4.8 Article

Adhesion and Surface Interactions of a Self-Healing Polymer with Multiple Hydrogen-Bonding Groups

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 24, 期 16, 页码 2322-2333

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201303013

关键词

self healing polymers; hydrogen bonding; adhesion; surface interactions; surface forces apparatus

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Foundation for Innovation (CFI)
  3. MRSEC Program of the National Science Foundation [DMR11-21053]
  4. US Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences [DE-FG02-87ER-45331]

向作者/读者索取更多资源

The surface properties and self-adhesion mechanism of self-healing poly(butyl acrylate) (PBA) copolymers containing comonomers with 2-ureido-4[1H]-pyrimidinone quadruple hydrogen bonding groups (UPy) are investigated using a surface forces apparatus (SFA) coupled with a top-view optical microscope. The surface energies of PBA-UPy4.0 and PBA-UPy7.2 (with mole percentages of UPy 4.0% and 7.2%, respectively) are estimated to be 45-56 mJ m(-2) under dry condition by contact angle measurements using a three probe liquid method and also by contact and adhesion mechanics tests, as compared to the reported literature value of 31-34 mJ m(-2) for PBA, an increase that is attributed to the strong UPy-UPy H-bonding interactions. The adhesion strengths of PBA-UPy polymers depend on the UPy content, contact time, temperature and humidity level. Fractured PBA-UPy films can fully recover their self-adhesion strength to 40, 81, and 100% in 10 s, 3 h, and 50 h, respectively, under almost zero external load. The fracture patterns (i.e., viscous fingers and highly self-organized parallel stripe patterns) have implications for fabricating patterned surfaces in materials science and nanotechnology. These results provide new insights into the fundamental understanding of adhesive mechanisms of multiple hydrogen-bonding polymers and development of novel self-healing and stimuli-responsive materials.

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