Mussel-inspired, self-healing polymer blends. (3rd June 2020)
- Record Type:
- Journal Article
- Title:
- Mussel-inspired, self-healing polymer blends. (3rd June 2020)
- Main Title:
- Mussel-inspired, self-healing polymer blends
- Authors:
- Song, Shengju
Yang, Haoyu
Cui, Yijie
Tang, Yifeng
Chen, Yanzheng
Yang, Biao
Yuan, Jikang
Huang, Jijun - Abstract:
- Abstract: Reversible dynamic covalent and noncovalent interactions are widely used to generate intrinsically self-healing polymers. However, nearly all approaches require sophisticated design and multi-stepped, tedious synthesis limited to weak hydrogels and rubbers, and pre-assume that high-modulus materials are more difficult to heal than low-modulus ones. Inspired by mussel foot proteins with the special amino acid unit of 3, 4-dihydroxy-l -phenylalanine, we develop a paradigm for achieving self-mendable polymer blends, composed of polyurethane (PU) as the matrix and poly(dopamine methacrylamide) (PDMA) as the dispersed phase. Healing efficiency increases from 24 to 32% for neat PU to 80–90% for the blends with increased moduli. This paradigm provides new insights into the role of mechanical properties in determining self-healing: high mechanical properties do not necessarily weaken self-repairability. The proof-of-concept enables easy modification of soft materials by solution mixing them with a polymer containing catechol groups, and thus opens up new applications in coatings, adhesives, antifouling, and biological engineering. Graphical abstract: Multiple adhesive proteins of mussels inspire to form polymer blends via solution polymerization. These blends are self-healable though the matrix of polyurethane contains no catechols, implying the essential roles of catechols in the dispersed phase (i.e., polydopamine methacrylamide) in rendering mendability. Image 1Abstract: Reversible dynamic covalent and noncovalent interactions are widely used to generate intrinsically self-healing polymers. However, nearly all approaches require sophisticated design and multi-stepped, tedious synthesis limited to weak hydrogels and rubbers, and pre-assume that high-modulus materials are more difficult to heal than low-modulus ones. Inspired by mussel foot proteins with the special amino acid unit of 3, 4-dihydroxy-l -phenylalanine, we develop a paradigm for achieving self-mendable polymer blends, composed of polyurethane (PU) as the matrix and poly(dopamine methacrylamide) (PDMA) as the dispersed phase. Healing efficiency increases from 24 to 32% for neat PU to 80–90% for the blends with increased moduli. This paradigm provides new insights into the role of mechanical properties in determining self-healing: high mechanical properties do not necessarily weaken self-repairability. The proof-of-concept enables easy modification of soft materials by solution mixing them with a polymer containing catechol groups, and thus opens up new applications in coatings, adhesives, antifouling, and biological engineering. Graphical abstract: Multiple adhesive proteins of mussels inspire to form polymer blends via solution polymerization. These blends are self-healable though the matrix of polyurethane contains no catechols, implying the essential roles of catechols in the dispersed phase (i.e., polydopamine methacrylamide) in rendering mendability. Image 1 Highlights: Poly(dopamine methacrylamide)/polyurethane blends were formed via solution polymerization. These PDMA/PU blends achieve superior self-healability even though the matrix contains no catechol groups. Self-healing is dominantly determined by the availability of PDMA rather than by mechanical properties. … (more)
- Is Part Of:
- Polymer. Volume 198(2020)
- Journal:
- Polymer
- Issue:
- Volume 198(2020)
- Issue Display:
- Volume 198, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 198
- Issue:
- 2020
- Issue Sort Value:
- 2020-0198-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-06-03
- Subjects:
- Mussel adhesive proteins -- Dopamine methacrylamide -- Self-healing -- Polymer blends -- Catechols
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2020.122528 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13488.xml