Premium
Rheological study of poly(ethylene glycol)/poly( N ‐isopropylacrylamide‐ co ‐2‐acrylamido‐2‐methylpropanesulphonic acid) semiinterpenetrating network formation
Author(s) -
Zhang Chi,
Easteal Allan J.
Publication year - 2004
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.21141
Subject(s) - comonomer , polymer chemistry , copolymer , ethylene glycol , rheometry , self healing hydrogels , poly(n isopropylacrylamide) , rheology , chemical engineering , materials science , chemistry , polymer , organic chemistry , composite material , engineering
The formation of a series of semiinterpenetrating network (SIPN) hydrogels made by free‐radical copolymerization of N ‐isopropylacrylamide (NIPA) and 2‐acrylamido‐2‐methylpropanesulphonic acid (AMPS) with varying comonomer mole ratios, crosslinked with N , N ′‐methylene‐bisacrylamide (MBAA) in the presence of poly(ethylene glycol) (PEG) with average molecular weight 6,000 g mol −1 was studied via determination of complex viscosity, η*, using plate–plate rheometry. The isothermal time dependence of η* at various temperatures or the variation of η* with temperature of pregel solutions was utilized to detect the onset of gelation. The SIPN systems were compared with the corresponding gels made under the same conditions in the absence of PEG. The copolymer mainchain composition has a major effect on the time or temperature for onset of gelation and in particular gelation appears to be inhibited to some extent by MBAA when the AMPS/NIPA mole ratio in the pregel solution exceeds 0.5. The presence or absence of PEG in pregel solutions has a lesser effect on gelation. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2083–2087, 2004