Novel synthesis of aluminum hydroxyfluorides AlFx(OH)3-x and application in E-1-chloro-3,3,3-trifluoropropene isomerization

被引:1
|
作者
Feng, Shiwei [1 ]
Zhang, Chengping [1 ]
Quan, Hengdao [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, 5 South Zhongguancun St, Beijing 100081, Peoples R China
关键词
Aluminum hydroxyfluoride; E-1-chloro-3; 3; 3-fluoropropene; Z-1-chloro-3; Lewis acid sites; Bronsted acid sites; CATALYTICALLY ACTIVE-SITES; FLUORINATED ALUMINA; ACID SITES; FLUORIDES; HYDROXIDE; ALKYLATION; CATALYSTS; CITRONELLAL; GAMMA-AL2O3; CYCLIZATION;
D O I
10.1016/j.mtchem.2023.101652
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile, safe, and environmentally friendly preparation method is described for the synthesis of AlFx(OH)3-x by the activation of y-Al2O3 using HCFO-1233zd(E) under various temperatures. Comprehensive characterization techniques including XRD, XPS, N2 sorption, SEM, TEM, 27Al MAS NMR, FTIR, and py-IR were employed, revealing that at lower temperatures such as 275 & DEG;C and 300 & DEG;C, the synthesis yielded AlF(OH)2, while at higher temperatures like 350 & DEG;C and 375 & DEG;C, pyrochlore AlF1.5(OH)1.5 and metastable hexagonal tungsten bronze-type (HTB) 13-AlF3 were formed, with a-AlF3 detected at 325 & DEG;C. Notably, a significant quantity of AlF(OH)2 can be obtained at 325 & DEG;C within a specific time frame. This amorphous phase exhibits weak Lewis acid sites and a lower acid density, rendering it significantly more effective in the isomerization of HCFO-1233zd(E) compared to strong Lewis acid catalysts such as AlF1.5(OH)1.5 and 13-AlF3, which could promote coke formation, leading to catalyst deactivation. Moreover, due to its limited further fluorination at 290 & DEG;C, the optimal catalyst exhibits prolonged lifespan and high efficiency in HCFO-1233zd(E) isomerization.& COPY; 2023 Elsevier Ltd. All rights reserved.
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页数:10
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