Water-soluble copolymers of 1-vinyl-2-pyrrolidone and acrylamide derivatives: Synthesis, characterization, and metal binding capability studied by liquid-phase polymer-based retention technique

Citation
Bl. Rivas et al., Water-soluble copolymers of 1-vinyl-2-pyrrolidone and acrylamide derivatives: Synthesis, characterization, and metal binding capability studied by liquid-phase polymer-based retention technique, J APPL POLY, 72(6), 1999, pp. 741-750
Citations number
28
Categorie Soggetti
Organic Chemistry/Polymer Science","Material Science & Engineering
Journal title
JOURNAL OF APPLIED POLYMER SCIENCE
ISSN journal
00218995 → ACNP
Volume
72
Issue
6
Year of publication
1999
Pages
741 - 750
Database
ISI
SICI code
0021-8995(19990509)72:6<741:WCO1AA>2.0.ZU;2-1
Abstract
Radical copolymerizations of 1-vinyl-2-pyrrolidone with acrylamide and N,N' -dimethylacrylamide at different feed ratios were investigated. The copolym ers were characterized by Fourier transform infrared spectroscopy, H-1 NMR, and C-13 NMR spectroscopy. The copolymer composition was determined from t he H-1 NMR spectra and found to be statistical. The metal complexation of p oly(acrylamide-co-1-vinyl-2-pyrrolidone) and poly(N,N'-dimethylacrylamide-c o-1-vinyl-2-pyrrolidone) for the metal ions Cu(II), Co(II), Ni(II), Cd(II), Zn(II), Pb(II), Fe(III), and Cr(III) were investigated in an aqueous phase . The liquid-phase polymer-based retention method is based on the retention of inorganic ions by soluble polymers in a membrane filtration cell and su bsequent separation of low-molecular compounds from the polymer complex for med. The metal ion interaction with the hydrophilic polymers was determined as a function of the pH and the filtration factor. Poly(N,N-dimethylacryla mide-co-2-vinyl-2-pyrrolidone) showed a higher affinity for the metal ions than poly(acrylamide-co-1-vinyl-2-pyrrolidone). According to the interactio n pattern obtained, Cr(III) and Cu(II) formed the most stable complexes at pH 7. Pb(II) and Zn(II) were not retained. (C) 1999 John Wiley & Sons, Inc.