Kinetics on thermal dissociation and oligomerization of dicyclopentadiene in a high temperature & pressure microreactor

被引:14
作者
Yao, Zhen [1 ]
Xu, Xin [1 ]
Dong, Yiling [3 ]
Liu, Xue [1 ]
Yuan, Bei [1 ]
Wang, Kai [2 ]
Cao, Kun [1 ]
Luo, Guangsheng [2 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Peoples R China
[2] Tsinghua Univ, Dept Chem Engn, State Key Lab Chem Engn, Beijing 100084, Peoples R China
[3] Indiana Univ, Coll Arts & Sci, Bloomington, IN 47405 USA
基金
中国国家自然科学基金;
关键词
Dicyclopentadiene; Thermal decomposition; Kinetics; Microreactor; Cyclopentadiene; OPENING METATHESIS POLYMERIZATION; DIELS-ALDER REACTIONS; NORBORNENE COPOLYMERS; PHASE CRACKING; CYCLOPENTADIENE; REACTOR; TRICYCLOPENTADIENE; NITRATION; CHEMISTRY; ETHYLENE;
D O I
10.1016/j.ces.2020.115892
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Dicyclopentadiene(DCPD) is an important 10-carbon olefin mostly derived from the pyrolysis of total petroleum hydrocarbons to ethylene. DCPD has two isomers, endo-dicyclopentadiene(endo-DCPD) and exodicyclopentadiene(exo-DCPD), and can be thermally decomposed into cyclopentadiene (CPD). This reaction is also reversible. A further addition reaction of CPD with endo-DCPD or exo-DCPD can produce tricyclopentadiene(TCPD). Using a microreactor, the kinetics of the decomposition and condensation of DCPD were investigated systematically at 5 MPa, 180-240 degrees C. The complete reaction rate and kinetic parameters of the reaction system were obtained in this work. The kinetic results showed that high temperature and short residence time were effective for obtaining more of the product, CPD. (C) 2020 Elsevier Ltd. All rights reserved.
引用
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页数:7
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