File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

석상일

Seok, Sang Il
Laboratory for Energy Harvesting Materials and Systems
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.endPage 1014 -
dc.citation.number 3 -
dc.citation.startPage 1008 -
dc.citation.title MATERIALS CHEMISTRY AND PHYSICS -
dc.citation.volume 112 -
dc.contributor.author Jana, Sunirmal -
dc.contributor.author Lim, Mi Ae -
dc.contributor.author Baek, In Chan -
dc.contributor.author Kim, Chang Hae -
dc.contributor.author Seok, Sang Il -
dc.date.accessioned 2023-12-22T08:13:42Z -
dc.date.available 2023-12-22T08:13:42Z -
dc.date.created 2016-02-14 -
dc.date.issued 2008-12 -
dc.description.abstract A silica-based inorganic-organic hybrid resins (IOHR) were synthesized by non-hydrolytic sol-gel process from 3-glycidoxypropyltrimethoxyrsi lane (GLYMO) and diphenylsilanediol (DPSD) at a fixed amount of (20 mol%) phenyltrimethoxysilane using barium hydroxide as a catalyst. The confirmation of condensation reaction in the IOHR was done by liquid state (29)Si NMR (Nuclear Magnetic Resonance) spectroscopy, measurement of viscosity as well as weight average molecular weight (W(m)) of the IOHR. The W(m) of the IOHR was varied from 1091 to 2151, depending upon the DPSD content. Fourier transform infrared (FTIR) spectroscopic measurements were performed to investigate the details of vibrational absorption bands in the IOHR. It was seen that up to 50 mol% of DPSD there were no absorption peaks in the region of 3000-3600 cm(-1) responsible for O-H groups and it reappeared at 60 mol% of DPSD due to some unreacted OH groups present in the resin. The IOHR at all the compositions was oily transparent liquid, miscible with various organic solvents like toluene, cyclohexanone, chloroform, tehrahydrofuran (THF), etc., and also commercial epoxy resins but immiscible with water. The color of the IOHR was pale yellow, which lightened with increasing DPSD content. The IOHR having 40-50 mol% ofDP5D were storable. The refractive index at 632.8 nm of the resin films varied from 1.556 to 1.588, depending upon the resin composition. Physico-chemical properties such as the thermal stability, visible transparency, etc. after curing were investigated as a function of the chemical composition. (C) 2008 Elsevier B.V. All rights reserved -
dc.identifier.bibliographicCitation MATERIALS CHEMISTRY AND PHYSICS, v.112, no.3, pp.1008 - 1014 -
dc.identifier.doi 10.1016/j.matchemphys.2008.06.070 -
dc.identifier.issn 0254-0584 -
dc.identifier.scopusid 2-s2.0-56049099993 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/18657 -
dc.identifier.url http://www.sciencedirect.com/science/article/pii/S0254058408004240 -
dc.identifier.wosid 000262183900052 -
dc.language 영어 -
dc.publisher ELSEVIER SCIENCE SA -
dc.title Non-hydrolytic sol-gel synthesis of epoxysilane-based inorganic-organic hybrid resins -
dc.type Article -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Sol-gel growth -
dc.subject.keywordAuthor Chemical synthesis -
dc.subject.keywordAuthor Optical materials -
dc.subject.keywordAuthor Coatings -
dc.subject.keywordPlus 3-GLYCIDYLOXYPROPYLTRIMETHOXYSILANE -
dc.subject.keywordPlus NANOCOMPOSITES -
dc.subject.keywordPlus SYSTEM -
dc.subject.keywordPlus FILMS -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.