4.2 Article

Structured Multistimuli-Responsive Functional Polymer Surfaces Obtained by Interfacial Diffusion of Amphiphilic Block Copolymers

期刊

出版社

WILEY
DOI: 10.1002/pola.23962

关键词

blends; block copolymers; interfaces; nanostructured interfaces; stimuli-sensitive polymers; surface functionalization; surface segregation; surfaces

资金

  1. Centre National de la Recherche Scientifique
  2. Agence National de la Recherche [ANR-07-JCJC-0148]
  3. Spanish National Research Council [PI 2008601037, MAT2009-12251, CCG08-CSIC/MAT-3643]
  4. Agence Nationale de la Recherche (ANR) [ANR-07-JCJC-0148] Funding Source: Agence Nationale de la Recherche (ANR)

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Herein, we report the preparation of structured multistimuli-responsive surfaces able to change reversibly both their chemical composition depending on the environment and their surface behavior by varying either/both the pH or/and the temperature. For that purpose, we took advantage of the surface segregation in homopolymer/diblock copolymer blends, composed of either polystyrene-block-poly(N,N'-dimethylaminoethylmethacrylate) (PS-b-PDMAEMA) or polystyrene-block-poly (N,N'-diethylaminoethylmethacrylate) (PS-b-PDEAEMA) and high molecular weight polystyrene used as a matrix. The variations of the surface composition as a function of the environment of exposure (air or water vapor) was investigated were investigated by XPS and contact angle measurements. The water-annealed surfaces contain PDMAEMA or PDEAEMA at the surface and are additionally able to respond both to pH and temperature as demonstrated by the Wilhelmy technique. Both PDMAEMA and PDEAEMA can switch from a hydrophilic state to a collapsed hydrophobic state increasing the temperature above the LCST. More interestingly, as a result of the microphase separation of the block copolymers at the interface, the surfaces of the blends exhibit structuration. Thus, either micellar structures or donut-like morphologies were obtained by using THF or toluene, respectively, as solvent. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1952-1961,2010

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