Insight into the Coke Precursor in the Process of the Methanol-to-Olefins Reaction

被引:16
|
作者
Zhang, Nini [1 ,2 ]
Zhu, Ruyue [1 ,2 ]
Chen, Sheng-Li [1 ,2 ]
Chen, Nan [1 ,2 ]
Cao, Yingqian [1 ,2 ]
Ma, Liya [1 ,2 ]
Wu, Tao [1 ,2 ]
Sun, Wei [1 ,2 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] China Univ Petr, Dept Chem Engn, Beijing 102249, Peoples R China
关键词
CATALYTIC CONVERSION; HYDROGEN-TRANSFER; SAPO-34; CATALYST; MOLECULAR-SIEVE; MTO REACTION; HYDROCARBONS; DEACTIVATION; MECHANISM; PATHWAYS; ACID;
D O I
10.1021/acs.energyfuels.9b02861
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In this work, formaldehyde formed in the methanol-to-olefins (MTOs) reaction was found to be a coke precursor on SAPO-34 and the amount of formaldehyde during the entire MTO reaction was measured accurately by the acetylacetone spectrophotometric method. The mechanism of formaldehyde formation, decomposition, and coking in the SAPO-34 molecular sieve in the methanol-to-olefins reaction was investigated. It was found that in the MTO reactor, the formed formaldehyde further condensed into coke on SAPO-34 where it was created and then traveled onto the downstream SAPO-34 and condensed into coke there. The higher the amount of formaldehyde in the MTO reaction, the higher the coking rate and the shorter the catalytic lifetime of SAPO-34. Physical mixing of MgO and SAPO-34 can slow down the coking rate and prolong the catalytic lifetime of SAPO-34 by decomposing the formaldehyde into CO, CO2, and H-2 on MgO.
引用
收藏
页码:742 / 748
页数:7
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