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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.
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页码:2695 / 2699
页数:5
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