Preparation of mesoporous silica-pillared H+-titanosilicates
- Authors
- Park, Kyeong-Won; Jung, Jong Hwa; Kim, Jong Duk; Kim, Sung-Kyu; Kwon, Oh-Yun
- Issue Date
- 1-Feb-2009
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Layered titanosilicate; Silica-pillaring; Intercalation; Template; Mesoporous material
- Citation
- MICROPOROUS AND MESOPOROUS MATERIALS, v.118, no.1-3, pp 100 - 105
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- MICROPOROUS AND MESOPOROUS MATERIALS
- Volume
- 118
- Number
- 1-3
- Start Page
- 100
- End Page
- 105
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/26395
- DOI
- 10.1016/j.micromeso.2008.08.021
- ISSN
- 1387-1811
1873-3093
- Abstract
- H+-titanosilicate (H4Ti2Si8O22 center dot 4H(2)O), formed by proton ion exchange of layered titanosilicate JDF-L1 (Na4Ti2Si8O22 center dot 4H(2)O) produced intercalation compounds in DDA (dodecylamine)-TEOS (tetraethylorthosilicate) solution. H+-titanosilicate/DDA/TEOS intercalation compounds rapidly hydrolyzed in pure water to form siloxane-pillared H+-titanosilicates. Calcination of siloxane-pillared H+-titanosilicates for 5 h at 500 degrees C in air resulted in the formation of mesoporous silica-pillared H+-titanosilicate (SPT) derivatives. SPT derivatives exhibited refractions corresponding to a basal spacing of 4.16-4.32 nm, a uniform pore size of 2.8-3.4 nm, and a large surface area of 535-618 m(2)/g. The structures and physical properties of SPT derivatives remained stable after heating for 5 h at 700 degrees C in air. These results indicate that DDA molecules have a decisive role in pore formation within SPT derivatives, because they act as a base catalyst and as a template, like surfactant micelles. during the hydrolysis of TEOS. (C) 2008 Elsevier Inc. All rights reserved.
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