HIGHER-ORDER STRUCTURE AND THERMORESPONSIVE PROPERTIES OF POLYMERIC GEL WITH CRYSTALLINE SIDE-CHAINS

Citation
Xw. He et al., HIGHER-ORDER STRUCTURE AND THERMORESPONSIVE PROPERTIES OF POLYMERIC GEL WITH CRYSTALLINE SIDE-CHAINS, Polymer Journal, 28(5), 1996, pp. 452-457
Citations number
15
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00323896
Volume
28
Issue
5
Year of publication
1996
Pages
452 - 457
Database
ISI
SICI code
0032-3896(1996)28:5<452:HSATPO>2.0.ZU;2-N
Abstract
Crosslinked polymeric gel films were prepared by a radical copolymeriz ation of stearyl acrylate (SA) and acrylic acid (AA) with N,N'-methyle nebisacrylamide (MBAA) as a cross-linker. Aggregation structure of the (SA/AA/MBAA, 24.7/74.3/1.0; molar ratio) gel film was investigated on the basis of X-ray diffraction study. The gel films in both a dried a nd a swollen states in dimethyl sulfoxide (DMSO) formed crystalline la mellar structure at room temperature owing to intermolecular aggregati on of stearyl acrylate side chains. The thermo-responsive behavior of the (SA/AA/MBAA) gel film was examined by the temperature dependence o f the swelling ratio. The swelling ratio of the (SA/AA/MBAA, 24.7/74.3 /1.0) gel film increased with an increase in temperature up to 320 K ( the melting temperature of stearyl acrylate side chain crystals), wher eas it decreased above 320 K. In order to improve the thermo-responsiv e behavior, the stretched gel film was prepared by uniaxial stretching . The magnitude of melting endotherm for the stretched (SA/AA/MBAA) ge l film increased with the stretching ratio and also, the crystallinity and/or the regularity of layer structure of the stretched gel him was improved by stretching, i.e. the lamellar long axis in the stretched gel aligned along the stretching direction. The thermo-responsive prop erties of the stretched gel films were also examined by the temperatur e dependence of the swelling ratio and the length of the gel film. The stretched gel film abruptly shrinked to the original length upon heat ing at melting temperature of stearyl acrylate side chain crystals.