Toughening diene elastomers by strong hydrogen bond interactions. (5th December 2016)
- Record Type:
- Journal Article
- Title:
- Toughening diene elastomers by strong hydrogen bond interactions. (5th December 2016)
- Main Title:
- Toughening diene elastomers by strong hydrogen bond interactions
- Authors:
- Luo, Ming-Chao
Zeng, Jian
Fu, Xuan
Huang, Guangsu
Wu, Jinrong - Abstract:
- Abstract: Introducing reversible hydrogen bonds as sacrificial bonds is an emerging strategy to improve the toughness of elastomers. However, binary hydrogen bonds are not strong enough and highly dynamic, and thus have only a moderate toughening effect. Here we demonstrate that quadruple hydrogen bonds have a remarkable toughening effect for diene elastomers. To fabricate the quadruple hydrogen bonds toughened elastomer, we graft 2-ureido-4[1H]-pyrimidinone (UPy) groups onto the backbone of polyisoprene (PI). The UPy groups dimerize to form strong hydrogen bonds which have higher bond energy than binary hydrogen bonds. Compared with weak hydrogen bonds with the same mole fraction, the strong hydrogen bonds lead to higher reversible crosslinking density and slower chain mobility of the elastomer; this enables higher energy dissipation as the elastomer is subjected to deformation. As a result, the introduction of UPy significantly increases both the toughness and the tensile strength of the elastomer. Moreover, unlike covalent sacrificial bonds, the hydrogen bonds of UPy are dynamic and show the re-association of sacrificial bonds at room temperature, as evidenced by recovery of hysteresis loop during cyclic tensile tests. This work will not only greatly extend our understanding on the different toughening effects of weak and strong hydrogen bonds, but also help us to rationally design tougher elastomers. Graphical abstract: Ashby plot in terms of toughness versus tensileAbstract: Introducing reversible hydrogen bonds as sacrificial bonds is an emerging strategy to improve the toughness of elastomers. However, binary hydrogen bonds are not strong enough and highly dynamic, and thus have only a moderate toughening effect. Here we demonstrate that quadruple hydrogen bonds have a remarkable toughening effect for diene elastomers. To fabricate the quadruple hydrogen bonds toughened elastomer, we graft 2-ureido-4[1H]-pyrimidinone (UPy) groups onto the backbone of polyisoprene (PI). The UPy groups dimerize to form strong hydrogen bonds which have higher bond energy than binary hydrogen bonds. Compared with weak hydrogen bonds with the same mole fraction, the strong hydrogen bonds lead to higher reversible crosslinking density and slower chain mobility of the elastomer; this enables higher energy dissipation as the elastomer is subjected to deformation. As a result, the introduction of UPy significantly increases both the toughness and the tensile strength of the elastomer. Moreover, unlike covalent sacrificial bonds, the hydrogen bonds of UPy are dynamic and show the re-association of sacrificial bonds at room temperature, as evidenced by recovery of hysteresis loop during cyclic tensile tests. This work will not only greatly extend our understanding on the different toughening effects of weak and strong hydrogen bonds, but also help us to rationally design tougher elastomers. Graphical abstract: Ashby plot in terms of toughness versus tensile strength, which includes PB-Urazole, Elastomer-Amide and hydroxyl, SBR-Zinc diacrylate, and PI-UPy. Highlights: The increase of toughness by incorporation of strong hydrogen bonds interactions. Quadruple hydrogen bonds disassociation during relaxation behavior and tensile process. Re-association behavior of quadruple hydrogen bonds. … (more)
- Is Part Of:
- Polymer. Volume 106(2016)
- Journal:
- Polymer
- Issue:
- Volume 106(2016)
- Issue Display:
- Volume 106, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 106
- Issue:
- 2016
- Issue Sort Value:
- 2016-0106-2016-0000
- Page Start:
- 21
- Page End:
- 28
- Publication Date:
- 2016-12-05
- Subjects:
- Toughness -- Diene elastomers -- Hydrogen bonds
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.2016.10.056 ↗
- 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:
- 1575.xml