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Synthesis of Small Crystal Size Y Zeolite Catalysts with High Hydrocracking Performance on n-Hexadecane
被引:11
作者:

Wang, Xiaohan
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Yu, Zhiqing
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Sun, Jinxiao
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Wei, Qiang
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Liu, Haoran
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Huang, Wenbin
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Zhao, Luyuan
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Si, Meng
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China

Zhou, Yasong
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China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
机构:
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
基金:
中国国家自然科学基金;
关键词:
HYDRODESULFURIZATION CATALYSTS;
GREEN SYNTHESIS;
NAY ZEOLITE;
IN-SITU;
ACIDITY;
SULFIDATION;
SAPO-11;
SUPPORT;
MODEL;
ISOMERIZATION;
D O I:
10.1021/acs.energyfuels.2c02851
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
A series of in situ dodecyl trimethyl ammonium bromide (DTAB)-modified small-crystal Y zeolites have been successfully synthesized by DTAB addition to the seed synthesis procedure, which was used to create the small crystal size Y zeolites. Compared to the Y zeolites prepared without DTAB, the Y zeolites prepared with DTAB have a uniform morphology and mesoporous structure, a larger specific surface area (up to 32.3 m2 g-1 increase), a smaller crystal size (up to 66 nm reduction), and more Bro''nsted acid sites (up to 55 mu mol/g increase). After loading with NiW, the corresponding NiW catalysts were utilized in the hydrocracking of n-hexadecane. It is evident from the catalytic performance that the catalysts containing DTAB-modified small -crystal zeolites have a higher yield and selectivity of primary cracking products compared with the Y zeolites without DTAB modification. Moreover, the conversion of n-hexadecane is also higher due to its low mass-transfer resistance, high dispersion, and sulfation of W species. When the molar ratio of DTAB/Al2O3 is 0.15, the corresponding catalyst has the optimum balance between cracking and hydro-dehydrogenation activity. Therefore, it has the most excellent catalytic performance and a 7.3% increase in C8-C12 yield.
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收藏
页码:13817 / 13832
页数:16
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