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Fabrication of ordered lamellar polyacrylamide/P123 composite membranes via solvent-evaporation-induced self-assembly.

作者信息

Tang Jing, Fan Yubing, Hu Jun, Liu Honglai

机构信息

Lab for Advanced Material and Department of Chemistry, East China University of Science and Technology, Shanghai 200237, People's Republic of China.

出版信息

J Colloid Interface Sci. 2009 Mar 1;331(1):191-5. doi: 10.1016/j.jcis.2008.11.033. Epub 2008 Dec 17.

DOI:10.1016/j.jcis.2008.11.033
PMID:19095244
Abstract

A series of composite membranes of poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) (P123) and polyacrylamide (PAM) have been successfully prepared by solvent-evaporation-induced self-assembly. Micellar self-assembly of P123 in aqueous solution plays an important role as a model for the formation of composite membranes. XRD patterns show that the synthesized compositions are in a lamellar mesostructure. The lattice spacing changes with P123 concentration: the higher the concentration of P123, the smaller the lattice spacing of the composite membranes. The data on sizes and zeta potentials of pure p-PAM aggregates, P123 micelles, p-PAM/P123 mixtures, and c-PAM/P123 composite aggregates suggest that interactions take place between PAM and P123 aggregations. The fabrication of the lamellar membranes via water-evaporation-induced self-assembly is recorded by fluorescent emission spectroscopy and dynamic light-scattering methods. Based on analysis of the results, a tentative mechanism for the formation of the lamellar membranes has been proposed.

摘要

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