The influence of aluminium sources on the acidic behaviour as well as on the catalytic activity of mesoporous H-AlMCM-41 molecular sieves

被引:106
作者
Sakthivel, A
Dapurkar, SE
Gupta, NM
Kulshreshtha, SK
Selvam, P
机构
[1] Indian Inst Technol, Dept Chem, Bombay 400076, Powai, India
[2] Bhabha Atom Res Ctr, Div Appl Chem, Bombay 400085, Maharashtra, India
[3] Bhabha Atom Res Ctr, Novel Mat & Struct Chem Div, Bombay 400085, Maharashtra, India
关键词
mesoporous materials; aluminium sources; butylation of phenol; AlMCM-41; TERTIARY BUTYLATION; T-BUTYLATION; PHENOL; MCM-41; ALKYLATION; STABILITY; ZEOLITES; STRENGTH; OXIDES;
D O I
10.1016/j.micromeso.2003.08.004
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of mesoporous molecular sieves (AIMCM-41) were synthesized with varying silicon-to-aluminium ratios and using three different aluminium sources, viz., sodium aluminate, aluminium isopropoxide and aluminium. sulphate. The samples were characterized systematically using XRD, TG-DTA, BET surface area, and ICP-AES. In addition, the extent of framework substitution as well as the nature of acid sites was deduced employing Al-27 MAS-NMR, pyridine FT-IR, and NH3-TPD methods. These studies indicate that in case of samples prepared with sodium aluminate, most of the aluminium existed in tetrahedral positions even after calcination. Also, such samples posses moderate-to-strong (Bronsted) acid sites along with small amounts of structural as well as non-framework Lewis acid sites. The density of non-framework acid sites depended upon the source of aluminium following a trend in the order of sodium aluminate < aluminium sulphate < aluminium isopropoxide. Among the various catalysts investigated, those having a silicon-to-aluminium ratio of around 60 irrespective of aluminum sources exhibited highest conversion and good selectivity for vapour phase tertiary-butylation of phenol. This characteristic is attributed to the presence of larger number of moderate-to-strong acid sites and a smaller number of Lewis acid sites. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:177 / 187
页数:11
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