TY - JOUR
T1 - Fast synthesis and morphology control of silicalite-1 in the presence of polyvinyl alcohol
AU - Ji, Weiwei
AU - Yao, Jianfeng
AU - Zhang, Lixiong
PY - 2011/8
Y1 - 2011/8
N2 - Silicalite-1 crystals with various morphologies were prepared by addition of polyvinyl alcohol (PVA) in silicalite-1 synthesis solution at 180 °C for 6-40 h. The samples were characterized by X-ray diffraction, scanning electron microscopy, FT-IR, thermogravimetric analysis and N2 sorption. PVA in the synthesis solution promoted the fast crystallization of silicalite-1 within 6 h due to its adsorption on the surface of silicalite-1 precursors and the hydrogen bonding effect. The addition of PVA would produce silicalite-1 without aggregation because PVA served as temporary physical barriers. However, more PVA in the system (weight ratio of PVA/SiO2 = 1.75) slowed down the nucleation rate of silicalite-1 as the high viscosity of PAV hindered the selectivity between PVA and crystal facet. PVA also changed the surface energy of silicalite-1 precursors, and resulted in silicalite-1 crystals with sizes from 6 × 2 × 0.6 to 15 × 10 × 3 μm3. Silicalite-1 crystals exhibited coffin-, plate-, and rod-like structure when different weight ratios of PVA/SiO2 were applied, and the silicalite-1 crystals had high BET surface areas of 485-513 m2/g.
AB - Silicalite-1 crystals with various morphologies were prepared by addition of polyvinyl alcohol (PVA) in silicalite-1 synthesis solution at 180 °C for 6-40 h. The samples were characterized by X-ray diffraction, scanning electron microscopy, FT-IR, thermogravimetric analysis and N2 sorption. PVA in the synthesis solution promoted the fast crystallization of silicalite-1 within 6 h due to its adsorption on the surface of silicalite-1 precursors and the hydrogen bonding effect. The addition of PVA would produce silicalite-1 without aggregation because PVA served as temporary physical barriers. However, more PVA in the system (weight ratio of PVA/SiO2 = 1.75) slowed down the nucleation rate of silicalite-1 as the high viscosity of PAV hindered the selectivity between PVA and crystal facet. PVA also changed the surface energy of silicalite-1 precursors, and resulted in silicalite-1 crystals with sizes from 6 × 2 × 0.6 to 15 × 10 × 3 μm3. Silicalite-1 crystals exhibited coffin-, plate-, and rod-like structure when different weight ratios of PVA/SiO2 were applied, and the silicalite-1 crystals had high BET surface areas of 485-513 m2/g.
KW - Microporous materials
KW - Morphology control
KW - Polymer hydrogel
KW - Silicalite-1
UR - http://www.scopus.com/inward/record.url?scp=79960263040&partnerID=8YFLogxK
U2 - 10.1007/s10934-010-9397-x
DO - 10.1007/s10934-010-9397-x
M3 - 文章
AN - SCOPUS:79960263040
SN - 1380-2224
VL - 18
SP - 451
EP - 454
JO - Journal of Porous Materials
JF - Journal of Porous Materials
IS - 4
ER -