摘要
Amorphous silica membranes were developed, based on an in silico molecular design, to exhibit excellent hydrogen-selective performance for separating hydrogen from mixtures containing larger organic molecules, such as methylcyclohexane and toluene. Triphenylmethoxysilane (TPMS) was synthesized and used as a novel precursor to prepare membranes by the counter-diffusion chemical vapor deposition method. Under the optimized bubbler temperature and counter-diffusion chemical vapor deposition reaction time, the fresh membranes showed high reproducibility and high hydrogen permeance in the order of 10(-6) mol m(-2) s(-1) Pa-1 and high H-2/SF6 ideal selectivity of over 12,000 at 573 K. Moreover, the TPMS-derived membrane exhibited good stability after hydrogen regeneration, even after placement in a dehumidifier cabinet at room temperature for 90 days. Single gas permeation performance and normalized Knudsen-based permeance evaluation showed that the TPMS-derived membrane (three phenyl groups on the precursor) had a pore size of 0.486 nm, and exhibited looser structures with larger pore size than those of a diphenyldimethoxysilane (DPDMS)-derived membrane (two phenyl groups on the precursor). These results suggest that the pore size of silica membranes can be tailored with various structured silica precursors containing phenyl groups.
- 出版日期2016-2-1
- 单位江西师范大学