催化作用
甲醇
水溶液
化学
壳聚糖
化学工程
双水相体系
金属
铜
吸附
氢
结合
制氢
色散(光学)
选择性
无机化学
有机化学
数学分析
工程类
物理
光学
数学
作者
Xiuting Wu,Zefeng Zheng,Liang Ma,Changsong Hu,Yunhong Pi,Tiejun Wang
标识
DOI:10.1016/j.ijhydene.2023.05.147
摘要
The aqueous-phase reforming of methanol(APRM)via non-precious metal heterogeneous catalysts is highly desirable, but challenging. Herein, we report a highly efficient copper catalyst encapsulated by chitosan-glucose (CS-G) conjugate with high metal loading of 35 wt% for H2 generation from APRM. The optimized Cu@CS19-G1-300 catalyst exhibited exceptional activity of 1.39 × 105 μmolH2/gcat/h at low temperature of 210 °C, which was ∼4.5 times higher than that of commercial CuZrAl catalysts (2.88 × 104 μmolH2gcat−1h−1). The chitosan-glucose conjugate acted not only as the main carbon support for Cu dispersion, but also as adsorbent to stablize as many Cu ions as possible. And meanwhile, with abundant Cu+/Cu0 interface sites due to the reducing effect of glucose, the water gas shift reaction (WGSR) was intensified and thus displayed excellent selectivity toward CO by-product. This specific catalyst construction for H2 production from APRM exhibits great potential of on-site H2 supply for polymer membrane fuel cells.
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