A hybrid kinetics integrating feed-consumption rate and product selectivity models for Fischer-Tropsch synthesis over an industrial cobalt-based catalyst

被引:6
作者
Niu, Congcong [1 ,2 ]
Guo, Shupeng [1 ]
Xia, Ming [1 ,3 ,7 ]
Wang, Jungang [1 ]
Jia, Litao [1 ,4 ]
Hou, Bo [1 ]
Wang, Baojun [5 ,6 ]
Li, Debao [1 ,4 ,8 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
[2] SINOPEC Res Inst Petr Proc Co Ltd, Beijing 100083, Peoples R China
[3] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[4] Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
[5] Taiyuan Univ Technol, State Key Lab Clean & Efficient Coal Utilizat, Taiyuan 030024, Shanxi, Peoples R China
[6] Taiyuan Univ Technol, Key Lab Coal Sci & Technol, Minist Educ & Shanxi Prov, Taiyuan 030024, Shanxi, Peoples R China
[7] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, 30 Puzhu South Rd, Nanjing 211816, Peoples R China
[8] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, 27 Taoyuan South Rd, Taiyuan 030001, Peoples R China
基金
中国国家自然科学基金;
关键词
Fischer-Tropsch synthesis; Kinetic model; CO consumption rate; Product selectivity model; PROMOTED IRON CATALYST; COMPREHENSIVE KINETICS; INTRINSIC KINETICS; DETAILED KINETICS; CO ACTIVATION; MECHANISM; OPTIMIZATION; REACTOR; WATER; HYDROGENATION;
D O I
10.1016/j.cej.2022.140817
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Intrinsic kinetic experiments were performed in a wide range of process conditions over an industrial Fischer-Tropsch Synthesis (FTS) cobalt-based catalyst to obtain the kinetic models, aiming at the process/engineering design and the elucidation of the reaction mechanism. A hybrid kinetic model including the CO consumption model based on the Langmuir Hinshelwood Hougen Watson (LHHW) reaction mechanism and the lump-type product distribution model-C19+ selectivity model was developed. The obtained model, through parameters' evaluation and optimization, could provide an excellent prediction of CO conversion and C19+ selectivity in a wide process condition range. Furthermore, it was inferred that CO activation follows direct dissociation mechanism with the hydrogenation of the dissociated C* and O* to CH* and OH* respectively as the rate determining step; and the activation energy for CO consumption rate model was obtained as 80.26 kJ mol- 1.
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页数:11
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