On the deactivation mechanism of zeolite catalyst in ethanol to butadiene conversion

被引:66
|
作者
Yan, Tingting [1 ,2 ]
Yang, Liu [1 ,2 ]
Dai, Weili [1 ,2 ,4 ]
Wang, Chuanming [5 ]
Wu, Guangjun [1 ,2 ,3 ]
Guan, Naijia [1 ,2 ,3 ]
Hunger, Michael [4 ]
Li, Landong [1 ,2 ,3 ]
机构
[1] Nankai Univ, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
[2] Nankai Univ, Natl Inst Adv Mat, Tianjin 300350, Peoples R China
[3] Nankai Univ, Collaborat Innovat Ctr Chem Sci & Engn, Minist Educ, Key Lab Adv Energy Mat Chem, Tianjin 300071, Peoples R China
[4] Univ Stuttgart, Inst Chem Technol, D-70550 Stuttgart, Germany
[5] SINOPEC Shanghai Res Inst Petrochem Technol, State Key Lab Green Chem Engn & Ind Catalysis, Shanghai 201208, Peoples R China
基金
中国国家自然科学基金;
关键词
Ethanol to butadiene; Deactivation mechanism; Zn-Y/Beta zeolite; Spectroscopy; Unsaturated aldehydes/ketones; TO-OLEFIN CONVERSION; SELECTIVE SYNTHESIS; MGO-SIO2; CATALYSTS; BIO-ETHANOL; 1,3-BUTADIENE; ACETALDEHYDE; LEBEDEV; CHEMISTRY; DRIFTS; OXIDES;
D O I
10.1016/j.jcat.2018.08.019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Despite of extensive attention on the ethanol to butadiene (ETB) conversion, the catalyst deactivation during ETB conversion is rarely investigated and poorly understood. Here, the mechanism of the catalyst deactivation during the ETB conversion over Zn-Y/Beta was investigated through several complementary approaches, including XPS, TGA, GC-MS, in situ DRIFTS, UV-vis and C-13 CP MAS NMR spectroscopy. Acetaldehyde was observed to be the first reactive intermediate formed in the ETB conversion, which was rapidly involved in a subsequent aldol condensation with the simultaneous production of acetone. Due to a self- and cross-condensation of acetaldehyde and acetone, long chain unsaturated aldehydes/ketones were formed and further converted to 2,4-dimethyl benzaldehyde via a cyclization reaction, which could gradually cover the active sites and led to catalyst deactivation. Fortunately, the deactivating species could be removed from catalyst surface via simple calcination and the complete regeneration of Zn-Y/Beta could be realized. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
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