The thermal properties and crystalline structure of the amphiphilic graft copolymers CR-g-PEG600, CR-g-PEG2000, and CR-g-PEG6000 using chloroprene rubber (CR) as the hydrophobic backbone and poly(ethylene glycol) (PEG) with different molecular weights as the hydrophilic side chains were studied by D
Side-chain crystallization behavior of graft copolymers consisting of an amorphous main chain and crystalline side chains. II. Poly(n-hexyl methacrylate)-graft-poly(ethylene glycol)
β Scribed by Katsuhiro Inomata; Chieko Fukuda; Kuniyoshi Hori; Hideki Sugimoto; Eiji Nakanishi
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 409 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
Abstract
The phase behavior and crystallization of graft copolymers consisting of poly(nβhexyl methacrylate) (PHMA) as an amorphous main chain and poly(ethylene glycol) (PEG) as crystallizable side chains (HMA__x__ with 15 β€ x β€ 73, where x represents the weight percentage of PEG) were investigated. Smallβangle Xβray scattering profiles measured above the melting temperature of PEG suggested that a microdomain structure with segregated PHMA and PEG domains was formed in HMA40 and HMA46. This phase behavior was qualitatively described by a calculated phase diagram based on the meanβfield theory. Because of the segregation of PEG into microdomains, the crystallization temperature of the PEG side chains in HMA__x__ was higher than that in poly(methyl acrylate)βgraftβpoly(ethylene glycol) having a similar value of x, which was considered to be in a disordered state above the melting temperature. In HMA__x__ with x β€ 40, PEG crystallization was strongly restricted, probably because the PEG microdomains were isolated in the PHMA matrix. As a result, the growth of PEG spherulite was not observed because the PEG crystallization occurred after vitrification of the PHMA segregated domains. Β© 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 129β137, 2007
π SIMILAR VOLUMES
To improve the hemocompatibility on hydrophobic biomedical materials by a simple coating technique, graft copolymers composed of a hydrophilic side chain with phospholipid polar groups and a hydrophobic backbone were synthesized. The hydrophilic chain had phospholipid polar groups, polyI2-methacrylo