Synthesis and characterization of a silica-alumina composite membrane and its application in a membrane reactor

被引:20
|
作者
Kageyama, Naoki [1 ]
Takagaki, Atsushi [1 ,2 ]
Sugawara, Takashi [1 ]
Kikuchi, Ryuji [1 ]
Oyama, S. Ted [1 ,2 ,3 ]
机构
[1] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[2] Fuzhou Univ, Coll Chem Engn, Fuzhou 350116, Fujian, Peoples R China
[3] Virginia Polytech Inst & State Univ, Dept Chem Engn 0211, Environm Catalysis & Nanomat Lab, Blacksburg, VA 24061 USA
关键词
Silica-alumina membrane; Chemical vapor deposition; Permeance mechanism; Steam methane reforming; Solubility site model; MICROPOROUS SILICA; GAS PERMEATION; HYDROGEN SEPARATION; PORE-SIZE; DIFFUSION; DEPOSITION; PD; STABILITY; HELIUM; STEAM;
D O I
10.1016/j.seppur.2017.12.021
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Hydrothermally stable silica-alumina composite membranes were synthesized through chemical vapor deposition (CVD) of tetraethylorthosilicate (TEOS) and aluminium tri-sec-butoxide precursor at 923 K on porous alumina supports. The membranes showed high hydrogen permselectivity (order of 10(-7) mol m(-2) s(-1)Pa(-1)) comparable to that of pure silica membranes but with superior hydrothermal stability, and were used in a membrane reactor. The permeation of small gas species (H-2, He, Ne) was well explained by a solid-state diffusion mechanism, involving jumps of the permeating species between solubility sites. The permeation mechanism of large gas molecules (CH4, CO2, N-2) was explained by the gas translation mechanism involving large pore defects. Steam methane reforming (SMR) on a Ni/MgO-SiO2 catalyst was carried out at 923 K in the membrane reactor and in a conventional packed-bed reactor. The membrane contributed to an increase in the hydrogen production rate by the selective extraction of hydrogen from the reaction zone.
引用
收藏
页码:437 / 445
页数:9
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