Remendable thermosetting polymers for isocyanate-free adhesives: a preliminary study. Issue 45 (28th September 2015)
- Record Type:
- Journal Article
- Title:
- Remendable thermosetting polymers for isocyanate-free adhesives: a preliminary study. Issue 45 (28th September 2015)
- Main Title:
- Remendable thermosetting polymers for isocyanate-free adhesives: a preliminary study
- Authors:
- Dolci, Elena
Michaud, Guillaume
Simon, Frédéric
Boutevin, Bernard
Fouquay, Stéphane
Caillol, Sylvain - Abstract:
- Abstract : Based on a model study, a new bis-cyclic monomer bearing a Diels–Alder adduct was synthesized. This monomer was polymerized with a diamine to yield a thermoresponsive polyhydroxyurethane (PHU). This PHU is remendable at around 100 °C by retro Diels–Alder reaction. Abstract : This study describes the synthesis and polymerization of a dicyclocarbonate Diels–Alder (DA) adduct to give a thermoresponsive non-isocyanate polyurethane (NIPU). Firstly a model adduct was synthesized by DA reaction between N -methylmaleimide and furfuryl cyclocarbonate ether (FCE). This adduct was characterized by 1 H-NMR and its thermal behavior was studied by 1 H-NMR, and differential scanning calorimetry (DSC). Then a telechelic dicyclocarbonate DA adduct was obtained by DA reaction between a bismaleimide oligomer and FCE in bulk with full conversion. Its thermal behavior was studied by thermogravimetric analysis (TGA) and DSC. The dicyclocarbonate adduct was polymerized by step-growth polymerization with a diamine, Jeffamine EDR148. The polymerization was performed at room temperature (in order to avoid adduct deprotection) with triazabicyclodecene as the catalyst. The obtained polymer was characterized by size exclusion chromatography (SEC) and 1 H-NMR. The polymer thermal behavior was fully characterized by three complementary analyses. By DSC, retro-Diels–Alder temperatures could be measured to be 90–120 °C. By a 1 H-NMR kinetic study at 100 °C, it could be shown that after 120 min atAbstract : Based on a model study, a new bis-cyclic monomer bearing a Diels–Alder adduct was synthesized. This monomer was polymerized with a diamine to yield a thermoresponsive polyhydroxyurethane (PHU). This PHU is remendable at around 100 °C by retro Diels–Alder reaction. Abstract : This study describes the synthesis and polymerization of a dicyclocarbonate Diels–Alder (DA) adduct to give a thermoresponsive non-isocyanate polyurethane (NIPU). Firstly a model adduct was synthesized by DA reaction between N -methylmaleimide and furfuryl cyclocarbonate ether (FCE). This adduct was characterized by 1 H-NMR and its thermal behavior was studied by 1 H-NMR, and differential scanning calorimetry (DSC). Then a telechelic dicyclocarbonate DA adduct was obtained by DA reaction between a bismaleimide oligomer and FCE in bulk with full conversion. Its thermal behavior was studied by thermogravimetric analysis (TGA) and DSC. The dicyclocarbonate adduct was polymerized by step-growth polymerization with a diamine, Jeffamine EDR148. The polymerization was performed at room temperature (in order to avoid adduct deprotection) with triazabicyclodecene as the catalyst. The obtained polymer was characterized by size exclusion chromatography (SEC) and 1 H-NMR. The polymer thermal behavior was fully characterized by three complementary analyses. By DSC, retro-Diels–Alder temperatures could be measured to be 90–120 °C. By a 1 H-NMR kinetic study at 100 °C, it could be shown that after 120 min at 100 °C, 85% of the adducts are deprotected. Finally, by SEC, it was demonstrated that the obtained NIPU polymer chains undergo thermal scission by rDA reaction. … (more)
- Is Part Of:
- Polymer chemistry. Volume 6:Issue 45(2015)
- Journal:
- Polymer chemistry
- Issue:
- Volume 6:Issue 45(2015)
- Issue Display:
- Volume 6, Issue 45 (2015)
- Year:
- 2015
- Volume:
- 6
- Issue:
- 45
- Issue Sort Value:
- 2015-0006-0045-0000
- Page Start:
- 7851
- Page End:
- 7861
- Publication Date:
- 2015-09-28
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5py01213a ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2762.xml