Hydroisomerization of long-chain n-alkanes over Pt/AlSBA-15+zeolite bimodal catalysts

被引:55
|
作者
Jaroszewska, Karolina [1 ]
Fedyna, Monika [1 ]
Trawczynski, Janusz [1 ]
机构
[1] Wroclaw Univ Sci & Technol, Fac Chem, 7-9 Gdanska, PL-50344 Wroclaw, Poland
关键词
Long-chain n-alkanes; Hydroisomerization; Cold flow properties; AlSBA-15; BEA; MOR; HEXADECANE HYDROISOMERIZATION; DECANE HYDROISOMERIZATION; PRODUCT SELECTIVITY; ALUMINA CATALYSTS; HYBRID CATALYSTS; CETANE NUMBER; METAL CONTENT; BETA-ZEOLITE; SI/AL RATIO; ACID SITES;
D O I
10.1016/j.apcatb.2019.117756
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
In this study, the Pt (0.5 wt%) catalysts supported on the bimodal composite materials consisting of AISBA-15 and zeolite (BEA or MOR) were used for hydroisomerization of the long-chain n-alkanes. Consideration was given to the method by which the AISBA-15 and zeolite (20 wt% concentration) were combined: (i) by adding the zeolite to AISBA-15 synthesis gel (Method 1) and (ii) by mechanical mixing the zeolite and AISBA-15 powders (Method 2). The experiments of hydroisomerization of n-hexadecane were carried out using a fixed bed flow reactor system (5 MPa; 260-360 degrees C; WSHV, 3.5 h(-1); H-2:CH, 350:1 Nm(3)/m(3)). It was found that the synthesis of the supports according to Method 1 resulted in a formation of new mesopores in the "zeolitic" phase of A1SBA-15 + zeolite, and also in a moderate acidity of these materials. The catalysts supported on the carriers prepared according to Method 1 exhibited higher activity and isomerization selectivity than these supported on the carriers prepared according to Method 2. The Method 1 yielded the Pt/AlSBA-15 + BEA catalyst displaying the highest isomerization selectivity (together with the highest contribution of monobranched isomers) and the lowest cracking selectivity.
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页数:11
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