4.7 Article

Characterization of microstructure of poly (N-isopropylacrylamide)-grafted polycarbonate track-etched membranes prepared by plasma-graft pore-filling polymerization

Journal

JOURNAL OF MEMBRANE SCIENCE
Volume 258, Issue 1-2, Pages 157-166

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.memsci.2005.03.012

Keywords

gating membranes; poly(N-isopropylacrylamide); polycarbonate track-etched membranes; plasma-graft pore-filling polymerization; microstructure; thermo-response

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Poly(N-isopropylacrylamide) (PNIPAM) was successfully grafted on the surfaces and in the pores of polycarbonate track-etched (PCTE) membranes by plasma-graft pore-filling polymerization method, and the microstructure of the PNIPAM-g-PCTE membrane was investigated systematically by employing XPS, SEM, FT-IR, AFM, contact angle instrument and water flux experiments. The results showed that, the grafted PNIPAM polymers were formed inside the pores throughout the entire membrane thickness, and there was not a dense PNIPAM layer formed on the membrane surface even at a pore-filling ratio as high as 76.1%. With the pore-filling ratio increasing, the pore diameters of PNIPAM-grafted membranes became smaller. When the pore-filling ratio was smaller than 44.2%, the pores of PNIPAM-g-PCTE membranes showed thermo-responsive gating characteristics because of the conformational change of grafted PNIPAM in the pores. On the other hand, when the pore-filling ratio was larger than 44.2%, the pores of membranes immersed in water were choked by the volume expansion of the grafted PNIPAM polymers, and the membranes did not show thermo-responsive gating characteristics any longer. The critical pore-filling ratio for choking the membrane pores was in the range from 30 to 40%. The contact angle of PNIPAM-g-PCTE membrane increased from 58.5 degrees to 87.9 degrees when the temperature changed from 25 to 40 degrees C. The thermo-responsive gating characteristics of the water flux of PNIPAM-g-PCTE membranes were mainly dependent on the pore size change rather than the variation of membrane/pore surface hydrophilicity. (c) 2005 Elsevier B.V. All rights reserved.

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