2010
DOI: 10.1021/ie101577r
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Synthesis and Characterization of Novel Poly(N-isopropylacrylamide-co-N,N′-dimethylaminoethyl methacrylate sulfate) Hydrogels

Abstract: Poly(N-isopropylacrylamide-co-N,N′-dimethylaminoethyl methacrylate sulfate) [P(NIPAM-co-DMAEMASA)] was prepared from N-isopropylacrylamide (NIPAM) and N,N-dimethylaminoethyl methacrylate sulfate (DMAEMASA) monomers, and its properties were compared with those of poly(N-isopropylacrylamide-co-N,N′-dimethylaminoethyl methacrylate) [P(NIPAM-co-DMAEMA)]. The copolymers were characterized by swelling measurements in distilled water (10-40 °C) and buffer solutions (I ) 0.1 M, pH ) 2.2-10.0), FTIR, DSC, and SEM metho… Show more

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Cited by 35 publications
(8 citation statements)
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“…The same effect was observed by Häntzschel et al in poly( N ‐vinyl caprolactam(VCL)‐ co ‐GM)‐based nanogels. As expected, the presence of a non‐responsive polymer led to a lower pH‐sensitivity . Moreover, it is well known that the pH‐responsiveness of polyelectrolyte‐based nanogels is governed by electrostatic interactions between the polymer chains, and therefore, it is determined by their charge density .…”
Section: Resultssupporting
confidence: 63%
“…The same effect was observed by Häntzschel et al in poly( N ‐vinyl caprolactam(VCL)‐ co ‐GM)‐based nanogels. As expected, the presence of a non‐responsive polymer led to a lower pH‐sensitivity . Moreover, it is well known that the pH‐responsiveness of polyelectrolyte‐based nanogels is governed by electrostatic interactions between the polymer chains, and therefore, it is determined by their charge density .…”
Section: Resultssupporting
confidence: 63%
“…Conventional PNIPAAm hydrogels are commonly initiated with TEMED/APS (or TEMED/KPS) redox pair and prepared by using an organic crosslinker such as BIS in water at temperatures T < VPTT . However, their high swelling ratios/slow shrinking rates, optical turbidities and mechanical weaknesses limit their application areas.…”
Section: Resultsmentioning
confidence: 99%
“…The intensity of the band at 1469 cm −1 is attributed to the bending of the CH bond in CH( CH 3 ) 2 . The peak at 1549 cm −1 represents the tertiary amine of the DMA unit, and the peaks at 3450 and 2919 cm −1 are characteristic indicators of the BODIPY moiety . The band at 1521 cm −1 is ascribed to the stretching of CC and C‐C in the thiophene ring.…”
Section: Resultsmentioning
confidence: 99%