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

被引:11
作者
Wang, Xiaohan [1 ]
Yu, Zhiqing [1 ]
Sun, Jinxiao [1 ]
Wei, Qiang [1 ]
Liu, Haoran [1 ]
Huang, Wenbin [1 ]
Zhao, Luyuan [1 ]
Si, Meng [1 ]
Zhou, Yasong [1 ]
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.
引用
收藏
页码:13817 / 13832
页数:16
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