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EnglishGraphene Oxide (GO) was prepared by chemical oxidation of high surface area graphite (G). GO was used to support ruthenium catalysts with the aim to activate self-healing reactions in multifunctional materials able to integrate simultaneously the healing reactions with the very interesting properties of graphene-based materials.Grubbs catalysts 1st (G1) and 2nd generation modified (G2 o-tol), Hoveyda-Grubbs catalysts 1st (HG1) and 2nd generation (HG2) were covalently bonded to GO preserving the same catalytic activity of the catalysts not bonded to the graphene sheets. GO-G2 o-tol and GO-G1deactivate during the process of preparation of the self-healing epoxy mixtures at 90°C. Evidence of the self-healing activity of the various catalytic complexes was investigated for both uncured and cured samples. Results show that GO-HG1 and GO-HG2 are not deactivated and hence they are able to trigger self-healing reaction based on the ROMP of 5-ethylidene-2-norbornene (ENB). This behavior is most likely due to the formation of 16 electron Ru-complexes that are more stable than the 14 electron complexes of GO-G1 and GO-G2 catalysts
| Titolo: | Synthesis of ruthenium catalysts functionalized graphene oxide for self-healing applications |
| Autori: | |
| Data di pubblicazione: | 2015 |
| Rivista: | |
| Abstract: | Graphene Oxide (GO) was prepared by chemical oxidation of high surface area graphite (G). GO was used to support ruthenium catalysts with the aim to activate self-healing reactions in multifunctional materials able to integrate simultaneously the healing reactions with the very interesting properties of graphene-based materials.Grubbs catalysts 1st (G1) and 2nd generation modified (G2 o-tol), Hoveyda-Grubbs catalysts 1st (HG1) and 2nd generation (HG2) were covalently bonded to GO preserving the same catalytic activity of the catalysts not bonded to the graphene sheets. GO-G2 o-tol and GO-G1deactivate during the process of preparation of the self-healing epoxy mixtures at 90°C. Evidence of the self-healing activity of the various catalytic complexes was investigated for both uncured and cured samples. Results show that GO-HG1 and GO-HG2 are not deactivated and hence they are able to trigger self-healing reaction based on the ROMP of 5-ethylidene-2-norbornene (ENB). This behavior is most likely due to the formation of 16 electron Ru-complexes that are more stable than the 14 electron complexes of GO-G1 and GO-G2 catalysts |
| Handle: | http://hdl.handle.net/11386/4647485 |
| Appare nelle tipologie: | 1.1.1 Articolo su rivista con DOI |
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