Sol-gel synthesis of mesoporous aluminosilicates with a narrow pore size distribution and catalytic activity thereof in the oligomerization of dec-1-ene

被引:34
作者
Agliullin, Marat R. [1 ,4 ]
Danilova, Irina G. [2 ]
Faizullin, Aidar V. [1 ]
Amarantov, Srgey V. [3 ]
Bubennov, Sergei V. [1 ]
Prosochkina, Tatyana R. [4 ]
Grigor'eva, Nelly G. [1 ]
Paukshtis, Evgeny A. [2 ]
Kutepov, Boris I. [1 ,4 ]
机构
[1] RAS, Inst Petrochem & Catalysis, St October Prospect 141, Ufa 450075, Russia
[2] RAS, AV Shubnikov Crystallog Inst, St Leninsky Prospekt 59, Moscow 119333, Russia
[3] RAS, Boreskov Inst Catalysis SB, Pr Akad Lavrentieva 5, Novosibirsk 630090, Russia
[4] Ufa State Petr Technol Univ, St Cosmonauts 1, Ufa 450062, Russia
关键词
Mesoporous aluminosilicates; Sol-gel synthesis; Bronsted and Lewis acidity; Oligomerization of dec-1-ene; ALUMINUM NITRATE NONAHYDRATE; SILICA-ALUMINA; ACIDIC PROPERTIES; POROUS PROPERTIES; AL-SBA-15; XEROGELS; SURFACE; IR; RECRYSTALLIZATION; AL-MCM-41;
D O I
10.1016/j.micromeso.2016.05.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Porous aluminosilicates with Si/Al ratio of 80 have been prepared by the sol-gel synthesis using tetraethyl orthosilicate (TEOS) and aluminum nitrate (Al(NO3)3*9H2O). It has been shown that the precipitation pH value and the gelation conditions strongly affected characteristics of the porous structure, the incorporation of aluminum into the silicate framework, and the surface acidity. It has been found that the implementation of the sol-gel synthesis initially in the acidic medium followed by the alkaline one allowed producing the mesoporous aluminosilicate with the specific surface area SBET of 660 m2 g(-1), the mesopore volume V of 0.74 cm3 g(-1), and the pore size distribution within the range of 2-5 nm. The high activity and selectivity of synthesized aluminosilicates in the oligomerization of dec-1-ene have been revealed. The conversion of dec-1-ene reached 92%. The formation selectivity of dec-1-ene oligomers with the oligomerization degree n = 2-3 amounted 87%. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 127
页数:10
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