Straightforward synthesis of poly(lauryl acrylate)-b-poly(stearyl acrylate) diblock copolymers by ATRP

被引:32
作者
Dutertre, Fabien [1 ]
Pennarun, Pierre-Yves
Colombani, Olivier [1 ]
Nicol, Erwan [1 ]
机构
[1] Univ Maine, Polymeres Colloides Interfaces UMR CNRS 6120, F-72085 Le Mans 09, France
关键词
Lauryl acrylate/dodecyl acrylate; Stearyl acrylate/octadecyl acrylate; Atom transfer radical polymerization (ATRP); Block copolymer; Semi-crystalline polymer; Thermoplastic elastomer; TRANSFER RADICAL POLYMERIZATION; SIZE-EXCLUSION CHROMATOGRAPHY; CHAIN-TRANSFER; BLOCK COPOLYMERIZATION; RENEWABLE RESOURCES; OCTADECYL ACRYLATE; MOLECULAR-WEIGHT; METHACRYLATE); POLYMERS; KINETICS;
D O I
10.1016/j.eurpolymj.2010.12.003
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Lauryl (LA) and stearyl (SA) acrylates were successfully polymerized by atom transfer radical polymerization (ATRP), leading to well defined homopolymers and diblock copolymers (PDI < 1.2). Interestingly, the polymerization was very well controlled using N,N,N',N '',N ''-pentamethyldiethylenetriamine (PMDETA), a ligand which had initially been reported to be unadvisable for the polymerization of such monomers. Both kinetic studies and chain extension reactions supported our conclusions. A PLA(65)-b-PSA(47) diblock copolymer was characterized by differential scanning calorimetry and dynamic thermo-mechanical analysis, revealing that both blocks exhibit side-chain crystallinity and phase segregate in the crystalline state. The diblock behaves as a brittle rigid polymer when both blocks are crystalline, as a ductile material after the melting of the PLA phase and becomes a viscous liquid when both blocks are molten. This work could be extended to the preparation of PSA-b-PLA-b-PSA bio-issued thermoplastic elastomers. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:343 / 351
页数:9
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