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In relation to this article, we declare that there is no conflict of interest.
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Received July 15, 2011
Accepted October 11, 2011
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Preparation of nanoporous films from self-assembled poly(vinyl chloride-g-methyl methacrylate) graft copolymer

Department of Chemical and Biomolecular Engineering, Yonsei University, 262, Seongsanno, Seodaemun-gu, Seoul 130-749, Korea
Korean Journal of Chemical Engineering, July 2012, 29(7), 959-963(5), 10.1007/s11814-011-0265-4
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Abstract

We report on the preparation of nanoporous films based on an amphiphilic graft copolymer of poly(vinyl chloride-graft-methyl methacrylate), i.e., PVC-g-PMMA. The PVC-g-PMMA graft copolymer was synthesized via atom transfer radical polymerization (ATRP), as confirmed by nuclear magnetic resonance spectroscopy (1H NMR), Fourier transform-infrared (FT-IR) spectroscopy, and gel permeation chromatography (GPC) analysis. The PVC-g-PMMA graft copolymer molecularly self-assembled into nanophase domains of PVC main chains and PMMA side chains, as revealed by wide angle X-ray scattering (WAXS) and transmission electron microscopy (TEM). The graft copolymer film prepared from tetrahydrofuran (THF), a good solvent for both chains, had a random microphase-separated morphology. However, when prepared from dimethyl sulfoxide (DMSO), a solvent selectively good for PVC, the film exhibited a micellar morphology consisting of a PMMA core and a PVC corona. Nanoporous films with different pore sizes and shapes were prepared through the selective etching of PMMA chains using a combined process of UV irradiation and acetic acid treatment.

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