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Facile ionothermal synthesis of SAPO-LTA zeotypes with high structural stability and their catalytic performance in MTO reaction.

Authors :
Lin, Yutong
Wei, Ying
Zhang, Ling
Guo, Ke
Wang, Miao
Huang, Pengfei
Meng, Xiangzhi
Zhang, Runduo
Source :
Microporous & Mesoporous Materials. Nov2019, Vol. 288, pN.PAG-N.PAG. 1p.
Publication Year :
2019

Abstract

Silicoaluminophosphate zeotype with LTA structure (SAPO-LTA) was prepared using ionothermal approach in commercial 1-ethyl-3-methyl imidazolium ([emim]+) ionic liquid. 1H→13C CP/MAS NMR, TGA and CHN elementary analysis results demonstrated that ionic liquid acted as single organic template occluded in pairs in each α cage of the structure. SAPO-LTA exhibited high structural stability after detemplation with excellent BET surface area and microporous volume. Silica content in the products increased with that in the initial reactants with a maximum of SiO 2 wt% lower than 5%. 29Si MAS NMR and NH 3 -TPD results further proved the incorporation of Si in the framework with improved acidity as compared with its aluminophosphate (AlPO) counterpart. SAPO-LTA was active in MTO reaction, showing higher butene and C 5+ product selectivity than that of SAPO-34 with CHA structure, and higher propene to ethylene and lower C 1 to C 4 alkane selectivity in comparison with that of high-silica LTA zeolite (LTA-HSZ). The deactivation of SAPO-LTA catalyst was due to the occlusion of bulky polyaromatic coke in the LTA structure, and could be perfectly recovered during three cycles of regeneration by high-temperature calcination. Image 1 • SAPO-LTA were ionothermally prepared in commercial [emim]+ ionic liquid. • Ionic liquid acted as single organic template occluded in pairs in each α cage of the structure. • The detemplated SAPO-LTA exhibited high structural stability with excellent texture property. • SAPO-LTA with improved acidity was active in MTO reaction showing unique product selectivity. • The deactivated SAPO-LTA could be perfectly recovered by high temperature calcination. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13871811
Volume :
288
Database :
Academic Search Index
Journal :
Microporous & Mesoporous Materials
Publication Type :
Academic Journal
Accession number :
137853182
Full Text :
https://doi.org/10.1016/j.micromeso.2019.109611