Synthesis of amphiphilic ethyl cellulose grafting poly(acrylic acid) copolymers and their self-assembly morphologies in water |
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Authors: | Hongliang Kang Wenyong Liu Benqiao He Dawa Shen Lin Ma Yong Huang |
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Affiliation: | a State Key Laboratory of Polymer Physics and Chemistry, Joint Laboratory of Polymer Science and Material, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China b Graduate University, Chinese Academy of Sciences, Beijing 100039, China c Laboratory of Cellulose and Lignocellulosics Chemistry, Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou 510650, China |
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Abstract: | Amphiphilic ethyl cellulose (EC)-g-poly(acrylic acid) (PAA) copolymers were synthesized by atom transfer radical polymerization (ATRP). Firstly, ethyl cellulose macro-initiators with the degree of the 2-bromoisobutyryl substitution of 0.04 and 0.25 synthesized by the esterification of the hydroxyl groups remained in EC macromolecular chains and the 2-bromoisobutyryl bromides. Secondly, tert-butyl acrylate was polymerized by ATRP with the ethyl cellulose macro-initiator and EC-g-PtBA copolymers were prepared. Finally, the EC-g-PAA copolymers were prepared by hydrolyzing tert-butyl group of the EC-g-PtBA copolymers. The grafting copolymers were characterized by means of GPC, 1H NMR and FTIR spectroscopies. The molecular weight of graft copolymers increased during the polymerization and the polydispersity was low. A kinetic study showed that the polymerization was first-order. Meanwhile, EC-g-PAA copolymers were self-assembled to micelles or particles with diameters of 5 nm and 100 nm in water (pH = 10) when the concentration was 1.0 mg/ml. |
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Keywords: | Ethyl cellulose-g-poly(acrylic acid) ATRP Self-assembly |
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