PPS/PA12 blending and characterization of reactive interface compatibilization

碩士 === 淡江大學 === 化學工程學系 === 85 === This research places emphasis upon the in-situ compatibilization reaction of PPS and PA12 in a blending formation process. It was generally observed that as small multi-functional molecules, maleic anhydrid...

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Main Authors: Huang, Ching-Jiunn, 黃清俊
Other Authors: Lin Dar-Jone
Format: Others
Language:zh-TW
Published: 1997
Online Access:http://ndltd.ncl.edu.tw/handle/27384948246658669658
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spelling ndltd-TW-085TKU000630022016-07-01T04:15:56Z http://ndltd.ncl.edu.tw/handle/27384948246658669658 PPS/PA12 blending and characterization of reactive interface compatibilization PPS/PA12摻合系統之相界面相容性反應研究與分析 Huang, Ching-Jiunn 黃清俊 碩士 淡江大學 化學工程學系 85 This research places emphasis upon the in-situ compatibilization reaction of PPS and PA12 in a blending formation process. It was generally observed that as small multi-functional molecules, maleic anhydride (MAH) and styrene, were employed the compatibility between these polymers were increased considerably. MAH and styrene were first grafted onto the ends of PPS to form an oligomeric chain of poly(MAH-co-styrene). Subsequently, the anhydride group of MAH was reacted with the terminal amino group of PA12. In these cases, FTIR spectrometry analysis indicated a high quantity of interfacial chain linkages between these polymers. Improvement of compatibility between PPS and PA12 as a result of in-situ grafting reactions were evidence from dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), rheometric analysis and scanning electronic microscopy (SEM). Lin Dar-Jone 林達鎔 1997 學位論文 ; thesis 99 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 淡江大學 === 化學工程學系 === 85 === This research places emphasis upon the in-situ compatibilization reaction of PPS and PA12 in a blending formation process. It was generally observed that as small multi-functional molecules, maleic anhydride (MAH) and styrene, were employed the compatibility between these polymers were increased considerably. MAH and styrene were first grafted onto the ends of PPS to form an oligomeric chain of poly(MAH-co-styrene). Subsequently, the anhydride group of MAH was reacted with the terminal amino group of PA12. In these cases, FTIR spectrometry analysis indicated a high quantity of interfacial chain linkages between these polymers. Improvement of compatibility between PPS and PA12 as a result of in-situ grafting reactions were evidence from dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), rheometric analysis and scanning electronic microscopy (SEM).
author2 Lin Dar-Jone
author_facet Lin Dar-Jone
Huang, Ching-Jiunn
黃清俊
author Huang, Ching-Jiunn
黃清俊
spellingShingle Huang, Ching-Jiunn
黃清俊
PPS/PA12 blending and characterization of reactive interface compatibilization
author_sort Huang, Ching-Jiunn
title PPS/PA12 blending and characterization of reactive interface compatibilization
title_short PPS/PA12 blending and characterization of reactive interface compatibilization
title_full PPS/PA12 blending and characterization of reactive interface compatibilization
title_fullStr PPS/PA12 blending and characterization of reactive interface compatibilization
title_full_unstemmed PPS/PA12 blending and characterization of reactive interface compatibilization
title_sort pps/pa12 blending and characterization of reactive interface compatibilization
publishDate 1997
url http://ndltd.ncl.edu.tw/handle/27384948246658669658
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AT huangchingjiunn ppspa12cànhéxìtǒngzhīxiāngjièmiànxiāngróngxìngfǎnyīngyánjiūyǔfēnxī
AT huángqīngjùn ppspa12cànhéxìtǒngzhīxiāngjièmiànxiāngróngxìngfǎnyīngyánjiūyǔfēnxī
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