Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)

碩士 === 國立臺灣大學 === 高分子科學與工程學研究所 === 102 === With precise synthetic control of hydrogen bond-rich side chains, shape memory polyurethanes (PUs) were prepared. These PUs comprising dendritic (DG series) or linear (LG series) polyurea/malonamide hydrogen bond-rich side chains with uniform chain lengths,...

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Main Authors: Yu-Ching Chen, 陳昱清
Other Authors: Ru-Jong Jeng
Format: Others
Language:zh-TW
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/42839677261525109839
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spelling ndltd-TW-102NTU053100162016-03-09T04:24:06Z http://ndltd.ncl.edu.tw/handle/42839677261525109839 Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide) 精準合成物理交聯型poly(urea/malonamide)側鏈之形狀記憶聚氨酯 Yu-Ching Chen 陳昱清 碩士 國立臺灣大學 高分子科學與工程學研究所 102 With precise synthetic control of hydrogen bond-rich side chains, shape memory polyurethanes (PUs) were prepared. These PUs comprising dendritic (DG series) or linear (LG series) polyurea/malonamide hydrogen bond-rich side chains with uniform chain lengths, providing physical crosslinking interactions to PUs. With the reactive functional group, azetidine-2,4-dione as the side chain of SPU to be a crosslinking site, different grafting ratios with various chain lengths of poly(urea/malonamides) were incorporated onto SPU. Consequently the physical crosslinking density could be adjusted. Via NMR, IR, EA, Mass and GPC analysis, we were able to confirm that the precise control of the poly (urea/malonamide) chain lengths were obtained. Differential scanning calorimeter (DSC) showed that, with the increasing chain length of the dendritic or linear poly (urea/malonamide), the glass transition temperature rose as a result of increasing hydrogen bonding interactions. Cyclic thermal-mechanical tests were conducted for evaluating shape memory properties. A higher E''low value would make the movement of the polymer chains limited at low temperatures. Consequently the shape retention was enhanced. Moreover, a significant phase transition peak (tanδmax) and a broad rubbery plateau region would also help to improve shape recovery. Because of this, SPU-DG series exhibited excellent shape retention, but relatively poor shape recovery. On the other hand, the SPU-LG series with higher generation side chains exhibited excellent shape and shape retention. S45-DG2.5-50, S45-DG2.5-25, S35-LG2.5-50, S45-LG2.5-50, S45-LG2.5-25 and S45-LG3.5-50 exhibited excellent shape memory effect, with both shape recovery and shape retention higher than 90%. It is concluded that these well-defined PUs with excellent shape-memory effect have been successfully developed in this work. Ru-Jong Jeng 鄭如忠 2014 學位論文 ; thesis 121 zh-TW
collection NDLTD
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description 碩士 === 國立臺灣大學 === 高分子科學與工程學研究所 === 102 === With precise synthetic control of hydrogen bond-rich side chains, shape memory polyurethanes (PUs) were prepared. These PUs comprising dendritic (DG series) or linear (LG series) polyurea/malonamide hydrogen bond-rich side chains with uniform chain lengths, providing physical crosslinking interactions to PUs. With the reactive functional group, azetidine-2,4-dione as the side chain of SPU to be a crosslinking site, different grafting ratios with various chain lengths of poly(urea/malonamides) were incorporated onto SPU. Consequently the physical crosslinking density could be adjusted. Via NMR, IR, EA, Mass and GPC analysis, we were able to confirm that the precise control of the poly (urea/malonamide) chain lengths were obtained. Differential scanning calorimeter (DSC) showed that, with the increasing chain length of the dendritic or linear poly (urea/malonamide), the glass transition temperature rose as a result of increasing hydrogen bonding interactions. Cyclic thermal-mechanical tests were conducted for evaluating shape memory properties. A higher E''low value would make the movement of the polymer chains limited at low temperatures. Consequently the shape retention was enhanced. Moreover, a significant phase transition peak (tanδmax) and a broad rubbery plateau region would also help to improve shape recovery. Because of this, SPU-DG series exhibited excellent shape retention, but relatively poor shape recovery. On the other hand, the SPU-LG series with higher generation side chains exhibited excellent shape and shape retention. S45-DG2.5-50, S45-DG2.5-25, S35-LG2.5-50, S45-LG2.5-50, S45-LG2.5-25 and S45-LG3.5-50 exhibited excellent shape memory effect, with both shape recovery and shape retention higher than 90%. It is concluded that these well-defined PUs with excellent shape-memory effect have been successfully developed in this work.
author2 Ru-Jong Jeng
author_facet Ru-Jong Jeng
Yu-Ching Chen
陳昱清
author Yu-Ching Chen
陳昱清
spellingShingle Yu-Ching Chen
陳昱清
Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)
author_sort Yu-Ching Chen
title Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)
title_short Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)
title_full Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)
title_fullStr Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)
title_full_unstemmed Side-chain physically reinforced SMPUs via precise architectures control of poly(urea/malonamide)
title_sort side-chain physically reinforced smpus via precise architectures control of poly(urea/malonamide)
publishDate 2014
url http://ndltd.ncl.edu.tw/handle/42839677261525109839
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