Abstract

ABSTRACTThermoresponsive and pH‐responsive gels were synthesized from N‐isopropyl acrylamide (NIPA) and N,N′‐dimethyl aminoethyl methacrylate (DMAEMA) monomers. Gelation reactions were carried out with both conventional free‐radical polymerization (CFRP) and controlled free‐radical polymerization [reversible addition fragmentation transfer (RAFT)] techniques. The CFRP gels were prepared by polymerizing mixtures of NIPA and DMAEMA in 1,4‐dioxane in presence of N,N'‐methylene bisacrylamide (BIS) as cross‐linker. The RAFT gels were prepared by a the polymerization of NIPA via a similar process in the presence of different amounts of poly(N,N′‐dimethyl aminoethyl methacrylate) macro chain‐transfer agent and the crosslinker. These gels were characterized by scanning electron microscopy (SEM) and differential scanning calorimetry. SEM analysis revealed a macroporous network structure for the RAFT gels, whereas their volume phase‐transition temperatures (VPTTs) were found to be in the range 32–34°C, close to that of poly(N‐isopropyl acrylamide) gels. However, the CFRP copolymer gels exhibited a higher VPTT; this increased with increasing DMAEMA content. The RAFT gels exhibited higher swelling capabilities than the corresponding CFRP gels and also showed faster shrinking–reswelling behavior in response to changes in temperature. All of the gels showed interesting pH‐responsive behavior as well. The unique structural attributes exhibited by the RAFT gels can potentially open up opportunities for developing new materials for various applications, for example, as adsorbents or carrier of drugs or biomolecules. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 42749.

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