化学
催化作用
二氧化碳
选择性
烯烃纤维
乙烯
玉米芯
碳纤维
生物量(生态学)
无机化学
有机化学
材料科学
复合材料
地质学
原材料
海洋学
复合数
作者
Lisheng Guo,Jian Sun,Xuewei Ji,Jian Wei,Zhiyong Wen,Ruwei Yao,Hengyong Xu,Qingjie Ge
标识
DOI:10.1038/s42004-018-0012-4
摘要
Abstract Although considerable efforts have been made in converting carbon dioxide to hydrocarbons via hydrogenation processes, precise control of C–C coupling towards heavy olefins remains a challenge. Here we report a carbon dioxide hydrogenation to olefin process that achieves 72% selectivity for alkenes and 50.3% selectivity for C 4–18 alkenes, of which formation of linear α-olefins accounts for 80%. The process is catalyzed by carbon-supported iron, commonly used in C–C coupling reactions, with multiple alkali promoters extracted from corncob. The design is based on the synergistic catalysis of mineral elements in biomass enzyme on which carbon dioxide can be directly converted into carbohydrate. The mineral elements from corncob may promote the surface enrichment of potassium, suppressing the secondary hydrogenation of alkenes on active sites. Furthermore, carburization of iron species is enhanced to form more Fe 5 C 2 species, promoting both the reverse water–gas shift reaction and subsequent C–C coupling.
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