Kinetics of hydroisomerization Of C5-C7 alkanes and their mixtures over platinum containing mordenite

被引:65
作者
Holló, A
Hancsók, J
Kalló, D
机构
[1] Univ Veszprem, Dept Hydrocarbon & Coal Proc, H-8201 Veszprem, Hungary
[2] Hungarian Acad Sci, Inst Chem, Chem Res Ctr, H-1525 Budapest, Hungary
关键词
kinetics; hydroisomerization; C-5-C-7; alkanes; hydrocarbon mixtures; platinum hydrogen-mordenite;
D O I
10.1016/S0926-860X(02)00018-2
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
The hydroisomerization of n-pentane (n-C-5), n-hexane (n-C-6), n-heptane (n-C-7), cvclohexane (C-C-6) and their binary mixtures, n-C-5/n-C-6, n-C-6/n-C-7, n-C-6/c-C-6, was investigated over platinum loaded hydrogen mordenite catalyst at 180-220degreesC, 5-40 bar total pressure and hydrogen to hydrocarbon molar ratios 1-20. The apparent activation energies of isomerization are 147, 123, 118 and 114 kJ/mol in case of n-C-5, n-C-6, n-C-7 and C-C-6, respectively, The reaction orders in alkane up to 4 bar are 0.33. 0.39, 0.15 and 0, 18, as well as the reaction orders in hydrogen up to 36 bar are -0.81. -0.65. - 1.08 and -0.57 for n-C5. n-C-6, n-C-7 and c-C-6, respectively. Rate equations were derived and parameters involved determined for the isomerization of pure paraffins. Kinetic results of n-C-5, n-C-6 and c-C-6 in lower pressure range ((Palkane). (PH2) less than or equal to 4 bar) suggest that the isomerization reaction on acid sites is rate-determining step, But in the case of n-C-7 or at higher pressures of n-C-6 and C-C-6 ((PH2 greater than or equal to) 20 bar, (Palkane) > 5 bar approximately), the zeolite micropore is getting filled with reactants resulting in diffusional inhibition. Experimental data for binary mixtures showed that the reaction rate of both components decreased on mixing. The component having higher boiling point exerts higher inhibiting effect on the hydroisomerization of more volatile alkane than inversely. Kinetic equations for binary mixtures were also proposed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:93 / 102
页数:10
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