Fischer-Tropsch Synthesis to Lower Olefins over Potassium-Promoted Reduced Graphene Oxide Supported Iron Catalysts

被引:233
作者
Cheng, Yi [1 ,2 ]
Lin, Jun [3 ]
Xu, Ke [1 ,2 ]
Wang, Hao [1 ,2 ]
Yao, Xuanyu [1 ,2 ]
Pei, Yan [1 ,2 ]
Yan, Shirun [1 ,2 ]
Qiao, Minghua [1 ,2 ]
Zong, Baoning [4 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] Chinese Acad Sci, Key Lab Nucl Anal Tech, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[4] SINOPEC, Res Inst Petr Proc, State Key Lab Catalyt Mat & Chem Engn, Beijing 100083, Peoples R China
来源
ACS CATALYSIS | 2016年 / 6卷 / 01期
基金
美国国家科学基金会;
关键词
iron catalysts; potassium promoter; reduced graphene oxide; Fischer-Tropsch synthesis; lower olefins; CARBON NANOTUBES; SYNTHESIS GAS; DIRECT CONVERSION; GRAPHITE OXIDE; LIGHT OLEFINS; ACTIVE PHASE; SYNGAS; HYDROGENATION; NANOPARTICLES; PERFORMANCE;
D O I
10.1021/acscatal.5b02024
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
Fischer Tropsch synthesis to lower olefins (FTO) opens up a compact and economical way to the production of lower olefin directly from syngas (CO and H-2) derived from natural gas, coal, or renewable biomass. The present work is dedicated to a systematic study on the effect of K in the reduced graphene oxide (rGO) supported iron catalysts on the catalytic performance in FTO. It is revealed that the activity, expressed as moles of CO converted to hydrocarbons per gram Fe per second (iron time yield to hydrocarbons, termed as FTY), increased first with the content of K, passed through a maximum at 646 mu mol(CO) g(Fe-1) s(-1) over the FeKl/rGO catalyst, and then decreased at higher K contents. Unlike the evolution of the activity, the selectivity to lower olefins increased steadily with K, giving the highest selectivity to lower olefins of 68% and an olefin/paraffin (O/P) ratio of 11 in the C-2-C-4 hydrocarbons over the FeK2/rGO catalyst. The volcanic evolution of the activity is attributed to the interplay among the positive effect of K on the formation of Hagg carbide, the active phase for FTO, and the negative roles of K in increasing the size of Hagg carbide at high content and blocking the active phase by K-induced carbon deposition. The monotonic increase in the selectivity to lower olefins is ascribed to the improved chain-growth ability and surface CO/H-2 ratio in the presence of K, which favorably suppressed the unwanted CH4 production and secondary hydrogenation of lower olefins.
引用
收藏
页码:389 / 399
页数:11
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