Bifunctional Ni2P/SAPO-11 catalyst for simultaneous hydroisomerization of 1-hexene and hydrodesulfurization of thiophene

被引:3
作者
Huang, Guan [1 ,2 ]
Sun, Zhichao [1 ,3 ]
Liu, Ying-Ya [1 ,3 ]
Yu, Zhiquan [2 ]
Wang, Yao [1 ]
Liu, Jiaxu [1 ]
Wang, Anjie [1 ,3 ]
Hu, Yongkang [1 ,4 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian Natl Lab Clean Energy, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[3] Dalian Univ Technol, Liaoning Key Lab Petrochem Technol & Equipments, Dalian 116024, Peoples R China
[4] SINOPEC, Dalian Res Inst Petr & Petrochem, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni-2; P/SAPO-11; 1-hexene; Hydroisomerization; Thiophene; Hydrodesulfurization; NICKEL PHOSPHIDE CATALYSTS; SAPO-11; MOLECULAR-SIEVE; METAL-ACID BALANCE; FCC GASOLINE; SKELETAL ISOMERIZATION; ACTIVE-SITE; N-OCTANE; SELECTIVE HYDROISOMERIZATION; ADSORPTION DESULFURIZATION; CRACKED GASOLINE;
D O I
10.1016/j.ces.2024.120714
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A bifunctional Ni2P/SAPO-11 catalyst for the upgrading of fluidized catalytic cracking (FCC) gasoline was constructed to achieve the simultaneous removal of sulfur and prevention of octane number loss. In the preparation of Ni2P/SAPO-11, a modification with an ammonia post-treatment led to improved dispersion and high catalytic performance. Adsorption and kinetic study demonstrated that thiophene preferentially and more strongly occupied the Ni2P sites, so as to inhibit the undesired saturation of 1-hexene and facilitate the parallel skeletal isomerization on Ni2P/SAPO-11. The concerted synergy of Ni2P crystallites for hydrodesulfurization and moderate Br & oslash;nsted acid sites of SAPO-11 for isomerization led to full conversion of thiophene and 1-hexene with 74 % selectivity to branched isomers at 320 degrees C and 1.5 MPa.
引用
收藏
页数:11
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