Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties

碩士 === 中原大學 === 化學工程研究所 === 95 === The aim of my study is to propose a method of modifying polymer, most polymers are inactive, and so we use modifying methods to functionlize it, in order to synthesize it with specific functional group, and to produce new living points, for it to synthesize with ot...

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Main Authors: Kuo-Chuan Lin, 林國權
Other Authors: Ying-Ling Liu
Format: Others
Language:zh-TW
Published: 2007
Online Access:http://ndltd.ncl.edu.tw/handle/16255302113973880572
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spelling ndltd-TW-095CYCU50630112015-10-13T13:55:57Z http://ndltd.ncl.edu.tw/handle/16255302113973880572 Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties 化學改質與官能化高分子之合成與性質研究 Kuo-Chuan Lin 林國權 碩士 中原大學 化學工程研究所 95 The aim of my study is to propose a method of modifying polymer, most polymers are inactive, and so we use modifying methods to functionlize it, in order to synthesize it with specific functional group, and to produce new living points, for it to synthesize with other monomers, and control its degree of functionalization. First, we use ozone treat method to produce Poly-vinylidene fluoride (PVDF) that that contains phenol functional group, and then we use it to react with benzoxazine, producing PVDF that contains benzoxazine functional group(we called PVDF-Bz);then we heat up the PVDF-Bz for it to cross-linking, then to product cross-linking structured PVDF membranes. Using Instron, we can defect the difference of mechanical property before and after the cross-linking process, and detect the cross-linking density also. Although PVDF’s main chains are broken by the high energy of ozone, such that the mechanical property is not as good as the untreated PVDF. But our new modifying method has successfully produced cross-linking PVDF. In the second experiment, we use chloromethylated method to pendent (-CH2Cl) group onto PSF’s specific phenyl , and then use the terminate of chlorine to initiate the Atom Transfer Radical Polymerization (ATRP) reaction, in order to polymerize the N-Isopropyl acryl amide (NIPAAm). By utilizing the different reaction time, we control the amount of NIPAAm. PSF-g-PNIPAAm polymer made micelles will amphiphilic according to different water temperatures. We therefore produce a kind of amphiphilic polymer that is sensitive to temperature. Next, we pendent polyhedral olgomeric silsesquioxane (POSS) into PSF, producing a kind of organic-inorganic hybrid materials, TGA test shows that this process produces a SiO2 protection layer on POSS, and therefore elevate it’s thermal stability within high temperature. POSS molecules to PSF form self-assembled architecture as the mole ratio of POSS is increased, the polymer’s dielectric constants of PSF-POSS were lower due to the increased free volume and the chain interaction. Ying-Ling Liu 劉英麟 2007 學位論文 ; thesis 125 zh-TW
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description 碩士 === 中原大學 === 化學工程研究所 === 95 === The aim of my study is to propose a method of modifying polymer, most polymers are inactive, and so we use modifying methods to functionlize it, in order to synthesize it with specific functional group, and to produce new living points, for it to synthesize with other monomers, and control its degree of functionalization. First, we use ozone treat method to produce Poly-vinylidene fluoride (PVDF) that that contains phenol functional group, and then we use it to react with benzoxazine, producing PVDF that contains benzoxazine functional group(we called PVDF-Bz);then we heat up the PVDF-Bz for it to cross-linking, then to product cross-linking structured PVDF membranes. Using Instron, we can defect the difference of mechanical property before and after the cross-linking process, and detect the cross-linking density also. Although PVDF’s main chains are broken by the high energy of ozone, such that the mechanical property is not as good as the untreated PVDF. But our new modifying method has successfully produced cross-linking PVDF. In the second experiment, we use chloromethylated method to pendent (-CH2Cl) group onto PSF’s specific phenyl , and then use the terminate of chlorine to initiate the Atom Transfer Radical Polymerization (ATRP) reaction, in order to polymerize the N-Isopropyl acryl amide (NIPAAm). By utilizing the different reaction time, we control the amount of NIPAAm. PSF-g-PNIPAAm polymer made micelles will amphiphilic according to different water temperatures. We therefore produce a kind of amphiphilic polymer that is sensitive to temperature. Next, we pendent polyhedral olgomeric silsesquioxane (POSS) into PSF, producing a kind of organic-inorganic hybrid materials, TGA test shows that this process produces a SiO2 protection layer on POSS, and therefore elevate it’s thermal stability within high temperature. POSS molecules to PSF form self-assembled architecture as the mole ratio of POSS is increased, the polymer’s dielectric constants of PSF-POSS were lower due to the increased free volume and the chain interaction.
author2 Ying-Ling Liu
author_facet Ying-Ling Liu
Kuo-Chuan Lin
林國權
author Kuo-Chuan Lin
林國權
spellingShingle Kuo-Chuan Lin
林國權
Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties
author_sort Kuo-Chuan Lin
title Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties
title_short Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties
title_full Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties
title_fullStr Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties
title_full_unstemmed Chemical modification and specificfunctionalization of polymers : Studieson the preparation and polymer properties
title_sort chemical modification and specificfunctionalization of polymers : studieson the preparation and polymer properties
publishDate 2007
url http://ndltd.ncl.edu.tw/handle/16255302113973880572
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