TY - JOUR
T1 - Marked inducing effects of metal oxide supports on the hydrothermal stability of zeolitic imidazolate framework (ZIF) membranes
AU - Kim, Jaesung
AU - Lee, Doohwan
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2016.
PY - 2016
Y1 - 2016
N2 - The thermal and hydrothermal stabilities and the structural degradation characteristics of a supported ZIF-7 membrane were studied at various temperatures (423-673 K), H2O vapor concentrations (10-40 mol%), and metal oxide supports (alumina, silica-alumina, silica, magnesia). The α-Al2O3 supported ZIF-7 membrane prepared by the seeding and secondary growth method exhibited a high H2 permeance (4.0 × 10-7 mol m-2 s-1 Pa-1) with high H2 selectivities (∼10) over larger CO, CH4, and CO2 gases at an elevated temperature of 573 K. The thermal stability of the membrane in a dry atmosphere was determined primarily by the intercrystalline grain boundaries on the ZIF-7 overlayer, exhibiting a high thermal stability at 573 K. However, considerable cracks developed through the grain boundaries at 673 K due to excessive thermal stress. It was found that the metal oxide supports markedly affect the hydrothermal stability of the ZIF membranes. The α-Al2O3 supported membrane suffered from fatal hydrothermal degradation of the ZIF-7 membrane layer even at a relatively low temperature of 473 K, and structural degradation was facilitated as the temperature and H2O vapor concentration increased. Surface acid/base properties of the metal oxide supports had a critical impact on the stability of the membrane; the ZIF-7 structure exhibited severe hydrothermal degradation on the acidic Al2O3 and SiO2-Al2O3 supports. Conversely, the ZIF-7 crystalline structure remained intact on the neutral SiO2 and basic MgO supports even under highly antagonistic hydrothermal conditions (573 K, 20 mol% H2O). These findings provide important new insights for the effective construction of ZIF membranes with improved structural stabilities under practically relevant thermal and hydrothermal operation conditions.
AB - The thermal and hydrothermal stabilities and the structural degradation characteristics of a supported ZIF-7 membrane were studied at various temperatures (423-673 K), H2O vapor concentrations (10-40 mol%), and metal oxide supports (alumina, silica-alumina, silica, magnesia). The α-Al2O3 supported ZIF-7 membrane prepared by the seeding and secondary growth method exhibited a high H2 permeance (4.0 × 10-7 mol m-2 s-1 Pa-1) with high H2 selectivities (∼10) over larger CO, CH4, and CO2 gases at an elevated temperature of 573 K. The thermal stability of the membrane in a dry atmosphere was determined primarily by the intercrystalline grain boundaries on the ZIF-7 overlayer, exhibiting a high thermal stability at 573 K. However, considerable cracks developed through the grain boundaries at 673 K due to excessive thermal stress. It was found that the metal oxide supports markedly affect the hydrothermal stability of the ZIF membranes. The α-Al2O3 supported membrane suffered from fatal hydrothermal degradation of the ZIF-7 membrane layer even at a relatively low temperature of 473 K, and structural degradation was facilitated as the temperature and H2O vapor concentration increased. Surface acid/base properties of the metal oxide supports had a critical impact on the stability of the membrane; the ZIF-7 structure exhibited severe hydrothermal degradation on the acidic Al2O3 and SiO2-Al2O3 supports. Conversely, the ZIF-7 crystalline structure remained intact on the neutral SiO2 and basic MgO supports even under highly antagonistic hydrothermal conditions (573 K, 20 mol% H2O). These findings provide important new insights for the effective construction of ZIF membranes with improved structural stabilities under practically relevant thermal and hydrothermal operation conditions.
UR - http://www.scopus.com/inward/record.url?scp=84962081928&partnerID=8YFLogxK
U2 - 10.1039/c5ta10190e
DO - 10.1039/c5ta10190e
M3 - Article
AN - SCOPUS:84962081928
SN - 2050-7488
VL - 4
SP - 5205
EP - 5215
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 14
ER -