TY - JOUR
T1 - Core-Shell-Structured Co-Z@TiO2 Catalysts Derived from ZIF-67 for Efficient Production of C5+ Hydrocarbons in Fischer-Tropsch Synthesis
AU - Wang, Hu
AU - Wu, Bingxia
AU - Cai, Yuan
AU - Zhou, Chengwei
AU - Feng, Nengjie
AU - Liu, Geng
AU - Chen, Chong
AU - Wan, Hui
AU - Wang, Lei
AU - Guan, Guofeng
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/5/15
Y1 - 2019/5/15
N2 - The core-shell-structured Co-Z@TiO2(N2+O2) catalyst, which was prepared by subsequent pyrolysis and calcination from precursor ZIF-67 coated by amorphous TiO2, was applied in Fischer-Tropsch synthesis (FTS). Compared with Co-Z@TiO2 catalyst, which was directly calcinated in air (Co-Z@TiO2(O2)) or pyrolyzed in N2 (Co-Z@TiO2(N2)), the Co-Z@TiO2(N2+O2) catalyst showed better dispersion, easier reducibility, and optimal metal cobalt particle size (8.4 nm) due to the intermediate pyrolysis treatment and core-shell structure. The Co-Z@TiO2(N2+O2) catalyst exhibited high cobalt time yield (14.84 μmolCO·gCo-1·s-1), high selectivity to C5+ (81.5%), and low selectivity to low carbon hydrocarbon (CH4 (12.7%) and C2-C4 (5.8%)). The core-shell structure could enhance diffusion limitations to transform intermediate products into heavier hydrocarbons. After 110 h of evaluation, the Co-Z@TiO2(N2+O2) catalyst still maintained good catalytic performance and cobalt particle size distribution.
AB - The core-shell-structured Co-Z@TiO2(N2+O2) catalyst, which was prepared by subsequent pyrolysis and calcination from precursor ZIF-67 coated by amorphous TiO2, was applied in Fischer-Tropsch synthesis (FTS). Compared with Co-Z@TiO2 catalyst, which was directly calcinated in air (Co-Z@TiO2(O2)) or pyrolyzed in N2 (Co-Z@TiO2(N2)), the Co-Z@TiO2(N2+O2) catalyst showed better dispersion, easier reducibility, and optimal metal cobalt particle size (8.4 nm) due to the intermediate pyrolysis treatment and core-shell structure. The Co-Z@TiO2(N2+O2) catalyst exhibited high cobalt time yield (14.84 μmolCO·gCo-1·s-1), high selectivity to C5+ (81.5%), and low selectivity to low carbon hydrocarbon (CH4 (12.7%) and C2-C4 (5.8%)). The core-shell structure could enhance diffusion limitations to transform intermediate products into heavier hydrocarbons. After 110 h of evaluation, the Co-Z@TiO2(N2+O2) catalyst still maintained good catalytic performance and cobalt particle size distribution.
UR - http://www.scopus.com/inward/record.url?scp=85064843258&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.9b00533
DO - 10.1021/acs.iecr.9b00533
M3 - 文章
AN - SCOPUS:85064843258
SN - 0888-5885
VL - 58
SP - 7900
EP - 7908
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 19
ER -