Hydroconversion of n-decane on Pt/HZSM-5 bifunctional catalysts: effect of the Si/Al ratio of the zeolite on selectivities

被引:7
|
作者
Soualah, Ahcene [1 ,2 ]
Lemberton, Jean-Louis [3 ]
Pinard, Ludovic [3 ]
Chater, Mohamed [1 ]
Magnoux, Patrick [3 ]
Moljord, Kjell [4 ]
机构
[1] USTHB, Fac Chim, LEPCMAE, El Alia 16111, Alger, Algeria
[2] Univ A Mira, Dept Genie Procedes, Bejaia 06000, Algeria
[3] Univ Poitiers, Fac Sci, Catalyse Chim Organ Lab, UMR CNRS 6503, F-86022 Poitiers, France
[4] Statoil Res Ctr, N-7005 Trondheim, Norway
关键词
Hydroconversion; n-Decane; Platinum; HZSM-5; zeolite; PRIMARY HYDROCRACKING MODES; LONG-CHAIN PARAFFINS; BETA-CATALYSTS; HYDROISOMERIZATION; ALKANES; PLATINUM; ISOMERIZATION; HEPTANE; ACID; RATIONALIZE;
D O I
10.1007/s11144-010-0193-z
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
Hydroconversion of n-decane was investigated on a series of platinum loaded ZSM-5 samples with varied Si/Al ratio. It was observed that the catalytic activity of ZSM-5 zeolite catalysts decreased with increasing Si/Al ratios in samples. The isomer selectivity in the platinum catalysts increased with the Si/Al ratio, which can be explained by a better balance between acidic and hydrogenating sites (high nPt/nH(+) ratio = 0.3). On this catalyst, the olefinic intermediates formed on Pt come into contact with few acidic sites before encountering a Pt particle again on which they hydrogenate to be transformed into branched isomers. Among the various C(10) isomers, 2-MeC(9) was preferentially formed. On all catalysts, the content of linear products in the carbon number fractions is higher than branched products. This result is interpreted by type C hydrocracking of methylnonanes.
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页码:209 / 219
页数:11
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