Kinetics of coke formation in the dimethyl ether-to-olefins process over SAPO-34 catalyst

被引:26
作者
Gao, Yuli [1 ]
Chen, Sheng-Li [1 ]
Wei, Yaqian [1 ]
Wang, Ya [1 ]
Sun, Wei [1 ]
Cao, Yingqian [1 ]
Zeng, Penghui [1 ]
机构
[1] China Univ Petr, Chem Engn Dept, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
基金
中国国家自然科学基金;
关键词
Dimethyl ether to olefins; Methanol to olefins; SAPO-34; Coking kinetics; METHANOL CONVERSION; LIGHT OLEFINS; ZEOLITE CATALYSTS; MOLECULAR-SIEVES; MTO PROCESS; DEACTIVATION; DEPOSITION; PERFORMANCE; MECHANISM; CRACKING;
D O I
10.1016/j.cej.2017.05.158
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A kinetic of coke formation during dimethyl ether (DME) conversion to light olefins over SAPO-34 was studied by the use of a thermogravimetry (TG) reactor. Coke formation experiments were conducted at the heating rate from 4 K/min to 10 K/min and DME partial pressure between 40.53 kPa and 101.325 kPa. The effects of reaction temperature, DME partial pressure and coke content of catalyst on coking rate were investigated. The results showed that high reaction temperature and DME partial pressure led to high coking rate. The coking rate increased with coke content during the early stage of the DME to olefins (DTO) reaction, indicating that the coking reaction was autocatalytic reaction. A mechanism was proposed for the coke formation and a kinetic equation was established to correlate the rate of coke formation with DME partial pressure, reaction temperature and coke content of catalyst. The activation energies of coke formation and adsorption of DME onto the active sites of catalyst surface in DTO reaction were found to be 99 kJ/mol and 49 kJ/mol, respectively. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:528 / 539
页数:12
相关论文
共 42 条
[1]   Dual-template synthesis of nanostructured CoAPSO-34 used in methanol to olefins: Effect of template combinations on catalytic performance and coke formation [J].
Aghamohammadi, Sogand ;
Haghighi, Mohammad .
CHEMICAL ENGINEERING JOURNAL, 2015, 264 :359-375
[2]  
Aguayo AT, 1999, J CHEM TECHNOL BIOT, V74, P315
[3]  
Albright L. F., 1979, DEPOSITION GASIFICAT
[4]  
Alexis J., 1945, IND ENG CHEM, V37, P318
[5]   Aluminium chloride: A new aluminium source to prepare SAPO-34 catalysts with enhanced stability in the MTO process [J].
Alvaro-Munoz, Teresa ;
Marquez-Alvarez, Carlos ;
Sastre, Enrique .
APPLIED CATALYSIS A-GENERAL, 2014, 472 :72-79
[6]  
Annaland TV, 2001, CATAL TODAY, V66, P427
[7]   Theoretical study of the methylbenzene side-chain hydrocarbon pool mechanism in methanol to olefin catalysis [J].
Arstad, B ;
Nicholas, JB ;
Haw, JF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (09) :2991-3001
[8]   CONVERSION OF METHANOL TO LOWER OLEFINS - KINETIC MODELING, REACTOR SIMULATION, AND SELECTION [J].
BOS, ANR ;
TROMP, PJJ ;
AKSE, HN .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1995, 34 (11) :3808-3816
[9]   The Prout-Tompkins rate equation in solid-state kinetics [J].
Brown, ME .
THERMOCHIMICA ACTA, 1997, 300 (1-2) :93-106
[10]  
Chen D, 1998, STUD SURF SCI CATAL, V119, P521