Dual-layer asymmetric microporous silica membranes

被引:190
作者
Tsai, CY
Tam, SY
Lu, YF
Brinker, CJ
机构
[1] Univ New Mexico, NSF, Ctr Micro Engn Mat, Albuquerque, NM 87106 USA
[2] Sandia Natl Labs, Adv Mat Lab, Albuquerque, NM 87106 USA
关键词
gas separations; inorganic membranes; membrane preparation and structure; microporous and porous membranes; CO2; removal;
D O I
10.1016/S0376-7388(99)00343-9
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
We report a novel sol-gel dip-coating process to form dual-layer microporous silica membranes with improved membrane performance and reproducibility. First, we deposit a surfactant-templated silica (STS) intermediate layer on top of a commercial gamma-alumina support both to improve its 'surface finish' and to prevent a subsequently deposited microporous overlayer from penetrating into the support. Second, membranes are processed under clean room conditions to avoid dust contamination, and third, membranes are vacuum-calcined to promote further pore shrinkage and impart surface hydrophobicity. The resulting asymmetric membrane exhibits a gradual change in pore diameter from 50 Angstrom (gamma-alumina support layer) to 10-12 Angstrom (STS intermediate layer), and then to 3-4 Angstrom (30 nm thick, ultramicroporous silica top-layer). Compared to a single-layer process using only the microporous overlayer, the dual-layer process improves both flux and selectivity. For the industrially important problem of natural gas purification, the combined CO2 flux ((3-0.5)x 10(-4) cm(3)(STP)/s/cm(2)/cm Hg) and CO2/CH4 separation factors (200-600) are superior to all previously reported values for the separation of a 50/50 (v/v) CO2/CH4 gas mixture. In addition, the membrane selectively separated hydrogen from a simulated reformate from partial oxidation of methanol as evidenced by a high concentration of hydrogen recovery. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:255 / 268
页数:14
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