Effect of temperature in the conversion of methanol to olefins (MTO) using an extruded SAPO-34 catalyst

被引:13
作者
Castellanos-Beltran, Ignacio Jorge [1 ]
Assima, Gnouyaro Palla [1 ]
Lavoie, Jean-Michel [1 ]
机构
[1] Univ Sherbrooke, CRIEC B, Sherbrooke, PQ J1L 2Y4, Canada
关键词
MTO; SAPO-34; temperature; extrusion; coke; light alkanes; TO-HYDROCARBONS; DIMETHYL ETHER; COKE FORMATION; LIGHT OLEFINS; MECHANISM; DEACTIVATION; PERFORMANCE; SELECTIVITY; CHEMISTRY; ZEOLITES;
D O I
10.1007/s11705-018-1709-8
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The methanol-to-olefin (MTO) reaction was investigated in a bench-scale, fixed-bed reactor using an extruded catalyst composed of a commercial SAPO-34 (65 weight percentage, wt-%) embedded in an amorphous SiO2 matrix (35 wt-%). The texture properties, acidity and crystal structure of the pure SAPO-34 and its extruded form (E-SAPO-34) were analyzed and the results indicated that the extrusion step did not affect the properties of the catalyst. Subsequently, E-SAPO-34 was tested in a temperature range between 300 and 500 degrees C, using an aqueous methanol mixture (80 wt-% water content) fed at a weight hour space velocity (WHSV) of 1.21 h(_1). At 300 degrees C, a low conversion was observed combined with the catalyst deactivation, which was ascribed to oligomerization and condensation reactions. The coke analysis showed the presence of diamandoid hydrocarbons, which are known to be inactive molecules in the MTO process. At higher temperatures, a quasi-steady state was reached during a 6 h reaction where the optimal temperature was identified at 450 degrees C, which incidentally led to the lowest coke deposition combined with the highest H/C ratio. Above 450 degrees C, surges of ethylene and methane were associated to a combination of H-transfer and protolytic cracking reactions. Finally, the present work underscored the convenience of the extrusion technique for testing catalysts at simulated scale-up conditions.
引用
收藏
页码:226 / 238
页数:13
相关论文
共 47 条
[1]   Neat dimethyl ether conversion to olefins (DTO) over HZSM-5: Effect of SiO2/Al2O3 on porosity, surface chemistry, and reactivity [J].
Al-Dughaither, Abdullah S. ;
de Lasa, Hugo .
FUEL, 2014, 138 :52-64
[2]   New Trends in Olefin Production [J].
Amghizar, Ismael ;
Vandewalle, Laurien A. ;
Van Geem, Kevin M. ;
Marin, Guy B. .
ENGINEERING, 2017, 3 (02) :171-178
[3]  
Bellussi G, 2005, STUD SURF SCI CATAL, V158, P1201
[4]   A methanol to olefins review: Diffusion, coke formation and deactivation SAPO type catalysts [J].
Chen, D. ;
Moljord, K. ;
Holmen, A. .
MICROPOROUS AND MESOPOROUS MATERIALS, 2012, 164 :239-250
[5]   Methanol conversion to light olefins over SAPO-34: kinetic modeling of coke formation [J].
Chen, D ;
Rebo, HP ;
Gronvold, A ;
Moljord, K ;
Holmen, A .
MICROPOROUS AND MESOPOROUS MATERIALS, 2000, 35-6 :121-135
[6]   Recent advancements in ethylene and propylene production using the UOP/Hydro MTO process [J].
Chen, JQ ;
Bozzano, A ;
Glover, B ;
Fuglerud, T ;
Kvisle, S .
CATALYSIS TODAY, 2005, 106 (1-4) :103-107
[7]   Study on the technology of thermal cracking of paraffin to alpha olefins [J].
Chen, Xinde ;
Yan, YongJie .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2008, 81 (01) :106-112
[8]   Pore-structure-mediated hierarchical SAPO-34: Facile synthesis, tunable nanostructure, and catalysis applications for the conversion of dimethyl ether into olefins [J].
Cui, Yu ;
Zhang, Qiang ;
He, Jie ;
Wang, Yao ;
Wei, Fei .
PARTICUOLOGY, 2013, 11 (04) :468-474
[9]   On the reaction mechanism for hydrocarbon formation from methanol over SAPO-34 .2. Isotopic labeling studies of the co-reaction of propene and methanol [J].
Dahl, IM ;
Kolboe, S .
JOURNAL OF CATALYSIS, 1996, 161 (01) :304-309
[10]  
ELLIOTT DC, 1988, ACS SYM SER, V376, P55