Structure鈥揜heology Relationship in Weakly Amphiphilic Block Copolymer Langmuir Monolayers

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• 作者：Giovanni Li Destri ; Fausto Miano ; Giovanni Marletta
• 刊名：Langmuir
• 出版年：2014
• 出版时间：April 1, 2014
• 年：2014
• 卷：30
• 期：12
• 页码：3345-3353
• 全文大小：394K
• 年卷期：v.30,no.12(April 1, 2014)
• ISSN：1520-5827

文摘

The linear viscoelastic behavior in the low-frequency regime at the water/air interface of three different polystyrene-b-poly(methyl methacrylate) (PS-b-PMMA) copolymer monolayers, with block length ratio varying from 66鈥?3 to 50鈥?0 and 25鈥?5 in molecular units, was studied and related to the interfacial behavior, characterized by means of Langmuir isotherms, and their structure, characterized by means of the atomic force microscopy technique. The two monolayers with the highest PMMA amount showed a single phase transition at about 12 mN/m, the viscoelastic behavior changing from a predominantly elastic to a viscoelastic one. This change in the viscoelastic properties was ascribed to the beginning of entanglement among the PMMA coronas of the predominantly circular quasi-2D micelles formed by the two copolymer systems. Conversely, the polymer with the lowest PMMA amount, despite having the same PMMA block length of the PS鈥揚MMA 50鈥?0 block copolymer, was found to behave as a viscoelastic system at any surface pressure value. This characteristic behavior cannot therefore be simply related to the molecular weight difference, but it has been put in connection to the irregular micelle structure observed in this case, consisting of a mixture of spherical and wormlike micelles, and to the different conformation adopted by the PMMA block. By blending this copolymer with an immiscible elastic homopolymer, namely poly(2-vinylpyridine), it was possible to tune the micelle nanostructure, obtaining regular circular quasi-2D micelles, with viscoelastic properties as expected for the PMMA-rich copolymer monolayers. To the best of our knowledge, this study shows for the first time the explicit dependence upon the relative block length and, in turn, upon the nanostructure of the quasi-2D micelles, of the viscoelastic properties of Langmuir monolayers and suggests that molecular weight and intermolecular interactions are not the only parameters governing the polymer conformation and, in turn, the polymer rheology and dynamics in quasi-2D confined systems.