Identifying the effective phosphorous species over modified P-ZSM-5 zeolite: a theoretical study

被引:32
作者
Chu, Yueying [1 ]
Gao, Xiuzhi [2 ]
Zhang, Xin [2 ]
Xu, Guangtong [2 ]
Li, Guangchao [1 ,3 ]
Zheng, Anmin [1 ,4 ]
机构
[1] Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Natl Ctr Magnet Resonance Wuhan, Wuhan 430071, Hubei, Peoples R China
[2] SINOPEC, State Key Lab Catalyt Mat & React Engn RIPP, Beijing 100083, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Wuhan Oxford Joint Catalysis Lab, Wuhan 430071, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
TEMPERATURE-PROGRAMMED DESORPTION; MODIFIED ZSM-5 ZEOLITE; CATALYTIC-CRACKING; HZSM-5; CATALYST; ACID STRENGTH; H-ZSM-5; METHANOL; OLEFINS; DEHYDRATION; CONVERSION;
D O I
10.1039/c8cp00946e
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
In this work, a density functional theory (DFT) study was carried out to address the fundamental description of the effective phosphorous species that could improve the framework stability and reduce the coke deposition formation on the P-ZSM-5 zeolite. On the basis of the dealumination barriers of ZSM-5 with all the possible phosphorous species bound on the zeolite framework, PO4H 4 was ascertained to be the effective phosphorous species that could improve the ZSM-5 zeolite hydrothermal stability and reduce its acid strength. Apart from this, the olefin polymerization reaction is the main cause of coking deactivation for ZSM-5. Thus, the effect of the modification P-ZSM-5 on the reactivity of light olefins dimerization was also studied. Compared to the unmodified ZSM-5, the activation energy of the rate-limiting step of ethylene dimerization was increased from 20.3 kcal mol(1) to 34.6 kcal mol (1), thereby apparently inhibiting ethylene dimerization and improving the resistance to coke deposition for P-ZSM-5. Our calculation results should provide a beneficial theoretical guide for designing and improving a catalyst for the methanol-to-olefins process and bioethanol dehydration.
引用
收藏
页码:11702 / 11712
页数:11
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