A comparison of two different flow types on performance of a thermally coupled recuperative reactor containing naphtha reforming process and hydrogenation of nitrobenzene

被引:22
作者
Iranshahi, D. [1 ]
Pourazadi, E. [1 ]
Bahmanpour, A. M. [1 ]
Rahimpour, M. R. [1 ]
机构
[1] Shiraz Univ, Sch Chem & Petr Engn, Dept Chem Engn, Shiraz 71345, Iran
关键词
Recuperative coupling; Catalytic naphtha reforming; Hydrogen production; Aromatic enhancement; Nitrobenzene hydrogenation; CATALYTIC-HYDROGENATION; MEMBRANE REACTOR; DEHYDROGENATION; DEACTIVATION; ETHYLBENZENE; ANILINE; STYRENE; DESIGN;
D O I
10.1016/j.ijhydene.2010.12.033
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
Refineries have been looking for proper ways of improving reformer performance by enhancing the octane number of the product via increasing the aromatics' compounds. To reach this goal, the endothermic catalytic naphtha reforming is coupled with the exothermic hydrogenation of nitrobenzene to aniline in a multifunctional heat exchanger reactor through the process intensification concept. Considering the higher thermal efficiency as well as the smaller size of the coupled reactor, utilizing this reactor is given priority. In this novel configuration, the first and the second reactor of the conventional naphtha reforming process are exchanged with the coupled reactors contain the endothermic naphtha reforming in the shell side and the hydrogenation reaction in the tube side. Both co-current and counter-current modes of flow are examined during the operation considering various studies in literature which show the superiority of co-current flow compared with the counter-current flow. The result of current study is compared with the corresponding results for conventional tubular reactor (CTR). The results show higher aromatic production as much as 18.73% and 16.48% in the co-current and counter-current mode, respectively. Hydrogen molar flow rate increases about 5 kmol/h by using countercurrent flow regime, compared with the CTR. Copyright (C) 2010, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3483 / 3495
页数:13
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