Preparation of BTESE-derived organosilica membranes for catalytic membrane reactors of methylcyclohexane dehydrogenation

被引:95
作者
Niimi, Takuya [1 ]
Nagasawa, Hiroki [1 ]
Kanezashi, Masakoto [1 ]
Yoshioka, Tomohisa [1 ]
Ito, Kenji [2 ]
Tsuru, Toshinori [1 ]
机构
[1] Hiroshima Univ, Grad Sch Engn, Dept Chem Engn, Higashihiroshima 7398527, Japan
[2] Natl Inst Adv Ind Sci & Technol, Natl Metrol Inst Japan, Tsukuba, Ibaraki 3058565, Japan
基金
日本学术振兴会;
关键词
Bis(triethoxysilyDethane (BTESE); Silica; Methylcyclohexane; Dehydrogenation; Membrane reactor; SEPARATION MEMBRANES; SILICA MEMBRANES; HYDROGEN; DIFFUSION; ANNIHILATION; ORGANIZATION; POSITRONIUM; PERMEATION; MIXTURES; METHANE;
D O I
10.1016/j.memsci.2014.01.003
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
High-performance organic-inorganic hybrid silica membranes were developed for use in membrane reactors for methylcyclohexane (MCH) dehydrogenation to toluene (TOL). The membranes were prepared via sol-gel processing using bis(triethoxysilyl)ethane (BTESE). In particular, the effect of hydrolysis conditions (H2O/BTESE molar ratio) on membrane performance was extensively investigated. Characterization based on TO-MASS, FTIR, N-2 adsorption and positron annihilation lifetime (PAL) measurements of BTESE-derived silica gels revealed that the ethoxides of BTESE were almost completely hydrolyzed and the silica networks became dense by increasing the H2O/BTESE molar ratio from 6 to 240. BTESE-derived silica membranes showed a hydrogen permeance that was higher than 1 x 10 mol/ (m(2) s Pa). H-2/TOL selectivity increased from 100 to 10,000 by increasing the H20/BTESE molar ratio from 6 to 240, while keeping a hydrogen permeance of more than 1 x 10(-6) mol/(m(2)s Pa). In MCH dehydrogenation, a BTESE-derived silica membrane reactor with a Pt/gamma-Al2O3/alpha-Al2O3 bimodal catalytic layer achieved MCH conversion of 75% that was higher than the equilibrium conversion of 60%, and a hydrogen purity in the permeate stream of more than 99.9% at 230 degrees C. 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:375 / 383
页数:9
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