On the extension of polysoaps: The Gaussian approximation

被引:2
作者
Borisov, OV
Halperin, A
机构
[1] INST CHEM SURFACES & INTERFACES,F-68057 MULHOUSE,FRANCE
[2] MAX PLANCK INST POLYMER RES,D-55021 MAINZ,GERMANY
关键词
D O I
10.1002/masy.19971130104
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polysoaps are linear hydrophilic chains that incorporate, at intervals, covalently bound amphiphilic monomers. In water, the amphiphilic monomers self assemble into intrachain micelles thus endowing the chain with a secondary structure. The relaxation of the secondary structure upon deformation qualitatively modifies the elastic behaviour of polysoaps in accordance with the LeChatelier principle. For long polysoaps a regime in which the tension in the chain, f, is independent of the end to end distance R, f similar to R degrees is predicted. The extension of long polysoaps is analysed for the particularly simple case when the backbone obeys Gaussian statistics and excluded volume interactions are neglected.
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页码:11 / 17
页数:7
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