Accession number:20090211853728
Title: Synthesis and characterization of amorphous poly(ethylene terephthalate) copolymers containing bis[4-(2-
hydroxyethoxy)phenyl]sulfone
Authors: Tsai, Yuhsin (1); Fan, Cheng-Hsing (1); Hung, Chi-Yuan (1);
Tsai, Fuu-Jen (2)
Author affiliation:(1) Nano-Powder and Thin Film Technology Center, Industrial Technology Research Institute, Tainan, Taiwan; (2)
Graduate Institute of Chinese Medical Science, China Medical University, Taichung, Taiwan; (3) Department of Medical Genetics, Pediatrics and Medical Research, China Medical University Hospital, Taichung, Taiwan; (4) Department of Biotechnology and
Bioinformatics, Asia University, Taichung, Taiwan Corresponding author:Tsai, Y.
Source title: European Polymer Journal Abbreviated source title:Eur Polym J Volume:45
Issue:1
Issue date:January 2009 Publication year:2009 Pages:115-122
Language:English ISSN:00143057 CODEN:EUPJAG
Document type:Journal article (JA)
Publisher:Elsevier Ltd, Langford Lane, Kidlington, Oxford, OX5 1GB, United Kingdom
Abstract:Poly(ethylene terephthalate) copolymers (abbreviated as PETS) that contain bis[4-(2-hydroxyethoxy)phenyl]sulfone (BHEPS) were prepared from dimethyl terephthalate (DMT), ethylene glycol (EG) (5-95%) and BHEPS (5-95%). The compositions and
microstructures of the copolyesters were determined by
<sup>1</sup>H and <sup>13</sup>C nuclear magnetic
resonance (NMR) spectroscopy, respectively. The thermal behaviors were studied over the entire range of copolymer compositions, using X-ray analysis, differential scanning calorimeter (DSC) and
thermogravimetric analysis (TGA). The molecular weights, optical characteristics and tensile properties of these polymers were also determined. Experimental results indicated that the copolymers had a random microstructure. The intrinsic viscosities of the copolymers ranged from 0.65 to 0.69 dL/g. The copolyesters with BHEPS of
<10 mol% were crystallizable, whereas the copolyesters with BHEPS of ≥10 mol% were amorphous. Incorporating BHEPS affected the glass-transition temperature (T<inf>g</inf>) values of those polymers, from about 81 °C for PETS<inf>5</inf> to 126
°C for PETS<inf>95</inf>. The optical transmissions exceeded 86% for λ = 400 nm for all of the amorphous polyesters.
The tensile modulus and strength of the copolyesters increased with BHEPS. However, they also became brittle and their elongation at break decreased. © 2008 Elsevier Ltd. All rights reserved.
Number of references:24
Main heading:Copolymerization
Controlled terms: Copolymers - Differential scanning calorimetry - Ethylene - Ethylene glycol - Glass transition - Glycols - Gravimetric analysis - Laser interferometry - Magnetic resonance -
Microstructure - Nuclear magnetic resonance - Nuclear magnetic resonance spectroscopy - Plastic products - Polyethylene
terephthalates - Polymers - Thermogravimetric analysis
Uncontrolled terms: Amorphous - Amorphous polies - Co polyesters - Copolymer compositions - Differential scanning calorimeters -
Dimethyl terephthalates - Elongation at breaks - Intrinsic viscosities - NMR - Optical characteristics - Optical transmissions - Phenyl sulfones - Poly(ethylene terephthalate) copolymer - Random
microstructures - Ray analyses - Synthesis and characterizations - Tensile modulus - Thermal behaviors - Transition temperatures
Classification code:815.2 Polymerization - 817.1 Polymer Products - 931.2 Physical Properties of Gases, Liquids and Solids - 931.3 Atomic and Molecular Physics - 815.1.1 Organic Polymers - 932.2 Nuclear Physics - 941.4 Optical Variables Measurements - 944.6 Temperature Measurements - 951 Materials Science - 933 Solid State Physics - 815.1 Polymeric Materials - 641.1 Thermodynamics - 701.2
Magnetism: Basic Concepts and Phenomena - 741.3 Optical Devices and Systems - 743.2 Holographic Applications - 531.2 Metallography - 744.9 Laser Applications - 801.4 Physical Chemistry - 802.3
Chemical Operations - 804.1 Organic Compounds - 801 Chemistry DOI:10.1016/j.eurpolymj.2008.10.007
Database:Compendex
Compilation and indexing terms, Copyright 2009 Elsevier Inc.