Ethylene oligomerization on nickel catalysts on a solid acid support: From New mechanistic insights to tunable bifunctionality

被引:35
|
作者
Koninckx, Elsa [1 ]
Mendes, Pedro S. F. [2 ]
Thybaut, Joris W. [2 ]
Broadbelt, Linda J. [1 ]
机构
[1] Northwestern Univ, McCormick Sch Engn & Appl Sci, Dept Chem & Biol Engn, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Univ Ghent, Lab Chem Technol, Technol Pk 125, B-9052 Ghent, Belgium
基金
美国国家科学基金会;
关键词
Ethylene oligomerization; Catalysis; Zeolite; Nickel; Bifunctional; OLEFIN OLIGOMERIZATION; ETHENE OLIGOMERIZATION; HETEROGENEOUS OLIGOMERIZATION; HIGHLY EFFICIENT; ACTIVE-SITES; DIMERIZATION; ZEOLITE; PROPENE; METAL; CONVERSION;
D O I
10.1016/j.apcata.2021.118296
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
Light alkene oligomerization on heterogeneous acidic catalysts is widely and successfully used in current commercial processes. However, ethylene oligomerization remains inefficient due to ethylene's inability to form reaction intermediates to a sufficient extent on acid sites. Adding Ni(II) on solid acids can more efficiently catalyze ethylene oligomerization and selectively produce butenes to fuel range products. The review proposes a complete and detailed mechanism of heterogenous Ni-catalyzed oligomerization, whose structures are supported by combining various studies throughout recent literature, and focuses on the bifunctional effects of the nickel and acid sites on ethylene oligomerization. Using experiments, first-principles calculations, and kinetic modeling, Ni2+ has been shown to selectively oligomerize ethylene to light, linear alkenes via the Cossee-Arlman mechanism, while Bronsted H+ sites catalyze further alkylation, cracking, and isomerization reactions. The effects of reaction conditions and catalyst properties on selectivity and activity for oligomerization are systematically discussed. Tuning the relative nickel-to-acid site ratio and the framework support can allow for an optimal catalyst design directed towards desirable products.
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页数:15
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