Hydroisomerisation of n-heptane over Pt/sulfated zirconia catalyst at atmospheric pressure

被引:14
作者
Oloye, F. F. [1 ,2 ]
Aliyev, R. [1 ]
Anderson, J. A. [1 ]
机构
[1] Univ Aberdeen, Sch Engn, Mat & Chem Engn, Surface Chem & Catalysis Grp, Aberdeen, Scotland
[2] Adekunle Ajasin Univ, Dept Chem Sci, Akungba Akoko, Nigeria
关键词
Hydroisomerisation; Catalyst; High and low temperature; Isomers; Cracked products; SOLID SUPERACID CATALYST; METAL-PROTON ADDUCT; SULFATED-ZIRCONIA; BUTANE ISOMERIZATION; PLATINUM; HYDROCRACKING; STATE; ACID; PT/SO42--ZRO2; HEXADECANE;
D O I
10.1016/j.fuel.2018.02.175
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
n-Heptane conversion was studied over Pt/sulfated zirconia catalyst using a fixed bed reactor at atmospheric pressure. Reaction temperature was varied between 453 and 723 K and the weight hourly space velocity was varied between 0.02 and 0.15 h(-1). The catalyst gave 96% selectivity to iso-heptane at ca. 9% conversion level (453 K). Furthermore, cracked products were only formed at higher conversions level through consecutive reaction routes. The only mono-branched product was 3-methyl hexane, while 2,3-dimethylpentane and 2,2-dimethylpentane were the other isomers. Under all conditions, selectivity to 2,3-dimethylpropane dominates because 2,2-dimethylpentane was cracked to iso-butane and propane. Both high temperature and low space velocity increase the conversion but lead to a significant decrease in isomer selectivity.
引用
收藏
页码:569 / 573
页数:5
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