Studies on Polymer/Carbon Black Composites by Heterocoagulation Method

碩士 === 國立臺灣大學 === 高分子科學與工程學研究所 === 101 === In this study, we synthesized micron-sized carbon black/polymer composites by heterocoagulation. First of all, we fabricated the polymeric latex with narrow size distribution and positive surface charge. Secondly, carbon black surface modification with sila...

Full description

Bibliographic Details
Main Authors: Hao Liu, 劉皓
Other Authors: Wen-Yen Chiu
Format: Others
Language:zh-TW
Published: 2013
Online Access:http://ndltd.ncl.edu.tw/handle/12329867176904837102
id ndltd-TW-101NTU05310006
record_format oai_dc
spelling ndltd-TW-101NTU053100062016-03-16T04:15:06Z http://ndltd.ncl.edu.tw/handle/12329867176904837102 Studies on Polymer/Carbon Black Composites by Heterocoagulation Method 以異質吸引法製備高分子/碳黑複合顆粒及其性質與應用研究 Hao Liu 劉皓 碩士 國立臺灣大學 高分子科學與工程學研究所 101 In this study, we synthesized micron-sized carbon black/polymer composites by heterocoagulation. First of all, we fabricated the polymeric latex with narrow size distribution and positive surface charge. Secondly, carbon black surface modification with silane coupling agent by sol-gel process had been achieved. In the last part, polymeric latex and surface-modified carbon black were mixed in water then we adjusted the pH value of the solution to a certain level and heated above the glass transition temperature of the polymeric latex to form carbon black/polymer composites. In the first part, we studied some experimental parameters that may affect the polydispersity, zeta potential, isoelectric point or Tg of the polymeric latex fabricated by dispersion polymerization. Dynamic light scattering zetasizer had been used to measure the zeta potential of the polymeric latex. We also used scanning electron microscopy(SEM) to measure the size of the latex particles. Glass transition temperature was measured by differential scanning calorimeter. In the second part, carbon black surface modification with various functional group on the silane coupling agents via sol-gel process had been studied. The size and its distribution of the modified carbon black were measured by dynamic light scattering and thermogravimetric analysis, then Fourier transform infrared spectrometer was used to confirm the results. In the last part, we fabricated the carbon black/polymer composites via heterocoagulation method. Appropriate pH values were controlled to achieve good heterocoagulation results. By heating up the polymeric latex to above its Tg, the surface of polymeric latex will become soft to form the stable composites with heterocoagulated carbon black on their surfaces. The composites were purified with centrifuge and the amount of the heterocoagulated carbon black was tested by thermogravimetric analysis. The morphologies of the cross section of the composites were observed via transmitting electron microscope ultra-thin sectioning technique. Wen-Yen Chiu 邱文英 2013 學位論文 ; thesis 89 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立臺灣大學 === 高分子科學與工程學研究所 === 101 === In this study, we synthesized micron-sized carbon black/polymer composites by heterocoagulation. First of all, we fabricated the polymeric latex with narrow size distribution and positive surface charge. Secondly, carbon black surface modification with silane coupling agent by sol-gel process had been achieved. In the last part, polymeric latex and surface-modified carbon black were mixed in water then we adjusted the pH value of the solution to a certain level and heated above the glass transition temperature of the polymeric latex to form carbon black/polymer composites. In the first part, we studied some experimental parameters that may affect the polydispersity, zeta potential, isoelectric point or Tg of the polymeric latex fabricated by dispersion polymerization. Dynamic light scattering zetasizer had been used to measure the zeta potential of the polymeric latex. We also used scanning electron microscopy(SEM) to measure the size of the latex particles. Glass transition temperature was measured by differential scanning calorimeter. In the second part, carbon black surface modification with various functional group on the silane coupling agents via sol-gel process had been studied. The size and its distribution of the modified carbon black were measured by dynamic light scattering and thermogravimetric analysis, then Fourier transform infrared spectrometer was used to confirm the results. In the last part, we fabricated the carbon black/polymer composites via heterocoagulation method. Appropriate pH values were controlled to achieve good heterocoagulation results. By heating up the polymeric latex to above its Tg, the surface of polymeric latex will become soft to form the stable composites with heterocoagulated carbon black on their surfaces. The composites were purified with centrifuge and the amount of the heterocoagulated carbon black was tested by thermogravimetric analysis. The morphologies of the cross section of the composites were observed via transmitting electron microscope ultra-thin sectioning technique.
author2 Wen-Yen Chiu
author_facet Wen-Yen Chiu
Hao Liu
劉皓
author Hao Liu
劉皓
spellingShingle Hao Liu
劉皓
Studies on Polymer/Carbon Black Composites by Heterocoagulation Method
author_sort Hao Liu
title Studies on Polymer/Carbon Black Composites by Heterocoagulation Method
title_short Studies on Polymer/Carbon Black Composites by Heterocoagulation Method
title_full Studies on Polymer/Carbon Black Composites by Heterocoagulation Method
title_fullStr Studies on Polymer/Carbon Black Composites by Heterocoagulation Method
title_full_unstemmed Studies on Polymer/Carbon Black Composites by Heterocoagulation Method
title_sort studies on polymer/carbon black composites by heterocoagulation method
publishDate 2013
url http://ndltd.ncl.edu.tw/handle/12329867176904837102
work_keys_str_mv AT haoliu studiesonpolymercarbonblackcompositesbyheterocoagulationmethod
AT liúhào studiesonpolymercarbonblackcompositesbyheterocoagulationmethod
AT haoliu yǐyìzhìxīyǐnfǎzhìbèigāofēnzitànhēifùhékēlìjíqíxìngzhìyǔyīngyòngyánjiū
AT liúhào yǐyìzhìxīyǐnfǎzhìbèigāofēnzitànhēifùhékēlìjíqíxìngzhìyǔyīngyòngyánjiū
_version_ 1718206318402076672