4.7 Article

Gelation of microsphere dispersions using a thermally-responsive graft polymer

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 396, 期 -, 页码 187-196

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2013.01.025

关键词

Particle gel; Network; Polycaprolactone; Thermoresponsive polymer; PMe(2)OMA; Isostrain; Isostress

资金

  1. Malaysian government
  2. EPSRC Centre for Innovative Manufacturing in Regenerative Medicine
  3. European Research Council under the European Community [227845]
  4. EPSRC
  5. EPSRC [EP/H028277/1] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/H028277/1] Funding Source: researchfish
  7. European Research Council (ERC) [227845] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Dispersions of microspheres (MSs) that form self-supporting particle gels are fundamentally interesting from the viewpoints of gel formation and mechanical properties. Here, we investigate model mixed MS/thermally responsive polymer dispersions that exist as particle gels at 37 degrees C. The MS comprised poly(caprolactone) (PCL) and was prepared by solvent evaporation. The thermally responsive polymer contained a cationic backbone and poly(2-(2-methoxyethoxy)ethyl methacrylate) side chains and is abbreviated as PMA. Mixed PCL/PMA dispersions formed weak gels due to depletion at 20 degrees C. At higher temperatures they formed stronger gels due to a combination of bridging of PCL MS by PMA and reinforcement by a PMA network. A key parameter controlling the mechanical properties of the reinforced MS particle gels was the volume fraction of PMA with respect to total polymer present (Phi(PMA)). Self-healing behaviour was observed for the gels Using dynamic rheology and this depended on Phi(PMA). The MS particle gel mechanical properties were conceptually described in terms of isostress and isostrain blending laws. At Phi(PMA) less than or greater than 0.057 the gels were dominated by the PCL or PMA networks, respectively. The latter value is suggested to be analogous to a phase inversion point. (C) 2013 Elsevier Inc. All rights reserved.

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