Plaques of poly(oxyethylene)-segmented polyurethanes prepared from isophorone diisocyanate (IPDI) and polyethylene glycol (PEG) were used to probe the structure/property relationships with regard to hydrophilicity, crystallinity and electrostatic dissipating (ESD) ability. The prepared urethane poly
Electrostatic dissipation and flexibility of poly(oxyalkylene)amine segmented epoxy derivatives
✍ Scribed by Lin, Jiang-Jen; Tseng, Feng-Po; Chang, Feng-Chih
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 147 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0959-8103
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✦ Synopsis
A family of hydrophilic and ¯exible epoxy polymers was prepared from the reaction of poly(oxyalkylene)amines and diglycidyl ether of bisphenol-A (DGEBA) at 1:1 molar ratio of NÐH to epoxide. The use of a high molecular weight (M W = 1000±6000) poly(oxyethylene±oxypropylene)amine and a low M W amine as curing agents provided epoxy materials with good properties in toughness and hydrophilicity. The hydrophilicity, probed by surface resistivity of these cured materials, was found to be affected by the nature and weight content of poly(oxyethylene) segment in the polymer backbone, and also by the degree of crystallinity. Speci®cally, in the presence of a water-soluble poly(oxy-ethylene±oxypropylene)diamine of M W 2000 the cured epoxies can reach surface resistivity as low as 10 8.6±9.6 V/&. In comparison, the water-insoluble poly(oxypropylene)diamine of M W 2000 afforded a higher surface resistivity of 10 10.5 V/& because of the difference in hydrophilicity between oxyethylene and oxypropylene functionalities. Poly(oxypropylene)diamine of M W 230 as the sole curing agent generated an epoxy with even higher surface resistivity of 10 13 V/& due to a highly crosslinking structure. With proper selection of mixed poly(oxyethylene±oxypropylene)diamine (25 wt%) and 2-aminoethanol (9 wt%), the DGEBA cured polymer had an appropriate surface resistivity of 10 9.8 V/& for antistatics. Moreover, this material was extremely ductile in appearance and showed over 500 % elongation at break during mechanical tests. The high ¯exibility is rationalized by the balanced chemical structure of poly(oxyalkylene) segments and bisphenol-A distributed in a slightly crosslinked system.
📜 SIMILAR VOLUMES
A family of Mannich bases were prepared from the reaction of 2,2-bis-(4hydroxyphenyl)propane (bisphenol A or BPA), formaldehyde, and poly(oxyalkylene)diamines at 1 : 1 : 1 or 1 : 2 : 2 molar ratio. By varying the molar ratio of bisphenol A to amine and the chemical structures of poly(oxyalkylene)dia