Study of the zeolite-catalyzed isomerization of 1-methylnaphthalene

被引:0
|
作者
Xing, Shiyong [1 ]
Cui, Yan [2 ,3 ]
Zhang, Fenglin [1 ]
Su, Jianbin [1 ]
Xu, Kan [1 ]
Liu, Xiaofei [2 ]
Chen, Ziheng [2 ]
Zhao, Yuehua [2 ]
Han, Minghan [2 ]
机构
[1] Beijing Special Engn Design & Res Inst, Beijing 100028, Peoples R China
[2] Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green Chem React Engn & Technol, Beijing 100084, Peoples R China
[3] PetroChina Co Ltd, Petrochem Res Inst, Beijing 100195, Peoples R China
关键词
CRUDE-OIL; ALKYLATION; MECHANISM; BEHAVIOR; BENZENE; BETA; 2,6-DIMETHYLNAPHTHALENE; DISPROPORTIONATION; DENITRIFICATION; INTERGROWTH;
D O I
10.1039/d4ra05881j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isomerization of 1-methylnaphthalene (1-MN) to 2-methylnaphthalene (2-MN) is a crucial step in the production of 2,6-dimethylnaphthalene (2,6-DMN), which is an important raw material for polyethylene naphthalate (PEN). Herein, the isomerization of 1-MN was systemically investigated over beta zeolite. Firstly, reaction conditions were systemically optimized, by which enhanced catalytic performance was obtained. Thereafter, the effect of nitride on the catalytic performance was investigated using a series of characterization techniques and DFT calculations, revealing that firm adsorption of nitride on acid sites was the main reason for catalyst deactivation. Activity of the deactivated catalyst was difficult to recover via extraction with hot benzene. Fortunately, catalytic performance could be effectively recovered through coke-burning, wherein the framework and acid sites were well-preserved during calcination.
引用
收藏
页码:38335 / 38344
页数:10
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