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作 者:耿承辉[1] 张飞[1] 高志贤[1] 周敬来[1] 任杰[2]
机构地区:[1]中国科学院山西煤炭化学研究所,山西太原030001 [2]浙江工业大学化工学院,浙江杭州310014
出 处:《石油学报(石油加工)》2005年第2期16-22,共7页Acta Petrolei Sinica(Petroleum Processing Section)
摘 要:以正十四烷(C14)在Pt/SAPO11催化剂上的临氢异构化为模型反应,探索了长链烷烃临氢异构化反应机制和产物分布的变化规律。结果表明,反应遵循含过渡态的平行顺序反应机制。温度升高,转化率、多支链异构体和裂解产物的收率持续升高,单支链异构体收率呈先升高后降低的变化规律;压力升高,转化率降低,单甲基异构体选择性明显提高;空速或n(H2)/n(C14)升高,转化率降低,单甲基异构体选择性呈升高趋势。随着反应转化率的升高,支链靠近碳链中心的单甲基异构体分布先增多然后趋于稳定。在压力0.5~1.5MPa、温度310~330℃条件下进行反应,可获得较佳的产物分布。The reaction mechanism of hydroisomerzation of n-tetradecane over Pt/SAPO-11 catalyst in a fixed bed down-flow reactor was studied. Results indicated that the reaction followed a parallel-sequential mechanism. As for the product distribution of the reaction, when reaction temperature increased, the total conversion, the yields of the multi-branching isomers and the cracked products kept increase, while the mono-branching isomers presented a tendency of firstly increased and then decreased. When the pressure increased, the conversion decreased, and the selectivity of the mono-methyl isomers increased significantly. When the space velocity or hydrogen to hydrocarbon mole ratio increased, the conversion decreased, and the mono-methyl isomers selectivity presented a tendency of increase. With the increase of conversion, the product distribution with respect to the mono-methyl isomers with the side-chain close to the center of the carbon chain increased at first and then went stabilized. The optimum product distribution was obtained at pressure of 0.5-1.5 MPa, temperature of 310-330°C.
关 键 词:临氢异构化 SAPO-11 长链烷烃 产物分布 催化剂
分 类 号:TQ426.94[化学工程] TE624.4[石油与天然气工程—油气加工工程]
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