Degradable epoxy resins prepared from diepoxide monomer with dynamic covalent disulfide linkage. (15th January 2016)
- Record Type:
- Journal Article
- Title:
- Degradable epoxy resins prepared from diepoxide monomer with dynamic covalent disulfide linkage. (15th January 2016)
- Main Title:
- Degradable epoxy resins prepared from diepoxide monomer with dynamic covalent disulfide linkage
- Authors:
- Takahashi, Akira
Ohishi, Tomoyuki
Goseki, Raita
Otsuka, Hideyuki - Abstract:
- Abstract: Development of a methodology for designing network polymers with both structural rigidity and facile degradability is an important challenge. In this paper, we demonstrate the efficient degradation of epoxy resins with disulfide linkages synthesized from bis(4-glycidyloxyphenyl)disulfide and several diamines. The synthesis was carried out without any undesired side-reactions derived from disulfide bonds, as supported by the structural characterization of the model linear polymer. While tensile testing revealed that the obtained resins possess comparable mechanical properties to the reference resin without disulfide bonds, they degraded into completely soluble fragments on a time-scale of several tens of minutes via disulfide exchange reaction in the presence of base. On the other hand, the resin containing disulfide bonds only at the diamine moieties only partially degraded and remained undissolved under the same conditions, which indicates that the design for fragmenting into smaller molecules is effective for the degradation of epoxy resins with dynamic disulfide linkages. Graphical abstract: Highlights: Epoxy resins with disulfide bonds in diepoxide moieties are synthesized. Model experiments indicated that target structure forms in cross-linked resins. Facile degradation was achieved on a time-scale of tens of minutes. Distribution of disulfide bonds in network affected degradation efficiency. Obtained resins show sufficient mechanical properties as ordinaryAbstract: Development of a methodology for designing network polymers with both structural rigidity and facile degradability is an important challenge. In this paper, we demonstrate the efficient degradation of epoxy resins with disulfide linkages synthesized from bis(4-glycidyloxyphenyl)disulfide and several diamines. The synthesis was carried out without any undesired side-reactions derived from disulfide bonds, as supported by the structural characterization of the model linear polymer. While tensile testing revealed that the obtained resins possess comparable mechanical properties to the reference resin without disulfide bonds, they degraded into completely soluble fragments on a time-scale of several tens of minutes via disulfide exchange reaction in the presence of base. On the other hand, the resin containing disulfide bonds only at the diamine moieties only partially degraded and remained undissolved under the same conditions, which indicates that the design for fragmenting into smaller molecules is effective for the degradation of epoxy resins with dynamic disulfide linkages. Graphical abstract: Highlights: Epoxy resins with disulfide bonds in diepoxide moieties are synthesized. Model experiments indicated that target structure forms in cross-linked resins. Facile degradation was achieved on a time-scale of tens of minutes. Distribution of disulfide bonds in network affected degradation efficiency. Obtained resins show sufficient mechanical properties as ordinary epoxy resin. … (more)
- Is Part Of:
- Polymer. Volume 82(2015)
- Journal:
- Polymer
- Issue:
- Volume 82(2015)
- Issue Display:
- Volume 82, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 82
- Issue:
- 2015
- Issue Sort Value:
- 2015-0082-2015-0000
- Page Start:
- 319
- Page End:
- 326
- Publication Date:
- 2016-01-15
- Subjects:
- Epoxy resins -- Dynamic covalent chemistry -- Degradation
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.2015.11.057 ↗
- 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:
- 1962.xml