Catalytic hydroconversion of aryl ethers over a nickel catalyst supported on acid-modified zeolite 5A

被引:18
|
作者
Yang, Zheng [1 ]
Wei, Xian-Yong [1 ,2 ]
Zhang, Min [1 ]
Zong, Zhi-Min [1 ]
机构
[1] China Univ Min & Technol, Minist Educ, Key Lab Coal Proc & Efficient Utilizat, Xuzhou 221116, Jiangsu, Peoples R China
[2] Ningxia Univ, State Key Lab High Efficiency Coal Utilizat & Gre, Yinchuan 750021, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni-TFMSA/TZ5A; Hydroconversion; Cyclohexane; C-O BONDS; MODEL COMPOUNDS; DIBENZYL ETHER; HYDROGENATION; NI; HYDROGENOLYSIS; REDUCTION; LIGNIN; HYDROCRACKING; OXIDE;
D O I
10.1016/j.fuproc.2018.04.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An active and recyclable supported Ni catalyst was developed by thermally decomposing nickel tetracarbonyl to highly dispersive nickel nanoparticles onto treated zeolite 5A (TZ5A) impregnated with trifluoromethanesulfonic acid (TFMSA). Oxybis(methylene)dibenzene (OBMDB) and benzyloxybenzene (BOB) were used as lignin-related model compounds (LRMCs) to evaluate Ni-13%-TEMSA/TZ5A activity for the catalytic hydroconversion (CHC) of the LRMCs. The results show that Ni13%-TFMSA/TZ5A effectively induces the formation and transfer of H+ and biatomic active hydrogen, and thereby catalyzes the CHC of OBMDB and BOB to afford cyclohexane under mild conditions. The CHC includes the cleavage of C-O and C-C bridged bonds, the hydrogenation of benzene ring, and dehydroxygenation of the resulting phenylmethanol and cyclohexanol. Ni-13%-TFMSA/TZ5A can be easily separated and still active for the CHC after 3-times recycle.
引用
收藏
页码:345 / 352
页数:8
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