Tandem catalytic synthesis of benzene from CO2 and H2

被引:29
作者
Zhu, Pengfei [1 ,3 ]
Sun, Jian [2 ]
Yang, Guohui [3 ]
Liu, Guoguo [3 ]
Zhang, Peipei [3 ]
Yoneyama, Yoshiharu [3 ]
Tsubaki, Noritatsu [3 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Environm Sci & Engn, Xian 710021, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
[3] Univ Toyama, Sch Engn, Dept Appl Chem, Gofuku 3190, Toyama 9308555, Japan
关键词
METHANE DEHYDROAROMATIZATION; DEHYDRO-AROMATIZATION; DIRECT CONVERSION; CARBON OXIDES; MO/HZSM-5; ZEOLITE; TEMPERATURE; PERFORMANCE;
D O I
10.1039/c7cy00842b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Benzene as an important raw material for production of industrial chemicals is generally synthesized from petroleum and coal tar. Here, we realized the synthesis of benzene from greenhouse CO2 and H-2 with two connected reactors by a tandem catalysis reaction comprising CO2 methanation and CH4 aromatization. The Ni/SiO2 catalyst loaded in the first reactor was used to convert CO2 to CH4, and the formed CH4 was sequentially converted to benzene on the Mo/HZSM-5 catalyst in the second reactor. The benzene formation rate reaches 0.68 mu molg(-1) min(-1) accompanied by a high CO2 conversion of 92%. This concept will provide a new pathway for the direct synthesis of benzene and CO2 utilization.
引用
收藏
页码:2695 / 2699
页数:5
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