Shape recovery and reprocessable polyurethanes crosslinked with double decker silsesquioxane via Diels-Alder reaction

In this work, a novel organic-inorganic polyurethane thermoset crosslinked with a difunctional polyhedral oligomeric silsesquioxanes (POSS) was synthesized via Diels-Alder (DA) reaction. First, a linear multi-segmented polyurethane with furan rings in the main chain (PU–F) was synthesized via the st...

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Veröffentlicht in:Polymer (Guilford) 2021-09, Vol.230, p.124042, Article 124042
Hauptverfasser: Zhao, Bingjie, Mei, Honggang, Hang, Guohua, Li, Lei, Zheng, Sixun
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Hang, Guohua
Li, Lei
Zheng, Sixun
description In this work, a novel organic-inorganic polyurethane thermoset crosslinked with a difunctional polyhedral oligomeric silsesquioxanes (POSS) was synthesized via Diels-Alder (DA) reaction. First, a linear multi-segmented polyurethane with furan rings in the main chain (PU–F) was synthesized via the step-growth polymerization of 4,4′-diphenylmethane diisocyanate (MDI) with poly(tetramethylene ether glycol) (PTMEG) and 2,5-furandimethanol. Second, 3,13-dimaleimido octaphenyl double decker silsesquioxane (3,13-dimaleimido DDSQ) was synthesized and used as the crosslinker of the linear PU-F. By adjusting the feed ratio of the difunctional POSS macromer (i.e., 3,13-dimaleimido DDSQ) to PU-F, the organic-inorganic PU thermosets (denoted DAPU-DDSQs) with variable densities of crosslinking were obtained. It was found that the DAPU-DDSQs were microphase-separated and that POSS cages were aggregated into the spherical microdomains, the sizes of which were 20–40 nm in diameter. It was demonstrated that the crosslinking in the DAPU-DDSQs had two aspects of contribution: i) the chemical crosslinking with D-A adducts between 3,13-dimaleimido DDSQ and PU-F and ii) the physical crosslinking with POSS microdomains via the aggregation of POSS cages. The DAPU-DDSQs displayed the improved thermomechanical properties with increasing 3,13-dimaleimido DDSQ incorporation. Owing to the formation of crosslinked structures, the DAPU-DDSQs displayed excellent shape memory properties. More importantly, the DAPU-DDSQs displayed the reprocessing (or recycling) properties at the temperature of retro DA reaction. The reprocessing properties of the DAPU-DDSQs can be utilized to re-edit the original shapes of shape memory PUs. Organic-inorganic polyurethane was crosslinked with a difunctional polyhedral oligomeric silsesquioxanes (POSS) via Diels-Alder (DA) reaction. The materials simultaneously had shape memory and reprocessing properties▪. •Organic-inorganic polyurethanes were crosslinked with POSS via Diels-Alder reaction.•The organic-inorganic polyurethanes displayed microphase-separated morphologies.•The POSS-crosslinked polyurethanes had shape memory and reprocessing (or recycling) properties.
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First, a linear multi-segmented polyurethane with furan rings in the main chain (PU–F) was synthesized via the step-growth polymerization of 4,4′-diphenylmethane diisocyanate (MDI) with poly(tetramethylene ether glycol) (PTMEG) and 2,5-furandimethanol. Second, 3,13-dimaleimido octaphenyl double decker silsesquioxane (3,13-dimaleimido DDSQ) was synthesized and used as the crosslinker of the linear PU-F. By adjusting the feed ratio of the difunctional POSS macromer (i.e., 3,13-dimaleimido DDSQ) to PU-F, the organic-inorganic PU thermosets (denoted DAPU-DDSQs) with variable densities of crosslinking were obtained. It was found that the DAPU-DDSQs were microphase-separated and that POSS cages were aggregated into the spherical microdomains, the sizes of which were 20–40 nm in diameter. It was demonstrated that the crosslinking in the DAPU-DDSQs had two aspects of contribution: i) the chemical crosslinking with D-A adducts between 3,13-dimaleimido DDSQ and PU-F and ii) the physical crosslinking with POSS microdomains via the aggregation of POSS cages. The DAPU-DDSQs displayed the improved thermomechanical properties with increasing 3,13-dimaleimido DDSQ incorporation. Owing to the formation of crosslinked structures, the DAPU-DDSQs displayed excellent shape memory properties. More importantly, the DAPU-DDSQs displayed the reprocessing (or recycling) properties at the temperature of retro DA reaction. The reprocessing properties of the DAPU-DDSQs can be utilized to re-edit the original shapes of shape memory PUs. Organic-inorganic polyurethane was crosslinked with a difunctional polyhedral oligomeric silsesquioxanes (POSS) via Diels-Alder (DA) reaction. 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First, a linear multi-segmented polyurethane with furan rings in the main chain (PU–F) was synthesized via the step-growth polymerization of 4,4′-diphenylmethane diisocyanate (MDI) with poly(tetramethylene ether glycol) (PTMEG) and 2,5-furandimethanol. Second, 3,13-dimaleimido octaphenyl double decker silsesquioxane (3,13-dimaleimido DDSQ) was synthesized and used as the crosslinker of the linear PU-F. By adjusting the feed ratio of the difunctional POSS macromer (i.e., 3,13-dimaleimido DDSQ) to PU-F, the organic-inorganic PU thermosets (denoted DAPU-DDSQs) with variable densities of crosslinking were obtained. It was found that the DAPU-DDSQs were microphase-separated and that POSS cages were aggregated into the spherical microdomains, the sizes of which were 20–40 nm in diameter. It was demonstrated that the crosslinking in the DAPU-DDSQs had two aspects of contribution: i) the chemical crosslinking with D-A adducts between 3,13-dimaleimido DDSQ and PU-F and ii) the physical crosslinking with POSS microdomains via the aggregation of POSS cages. The DAPU-DDSQs displayed the improved thermomechanical properties with increasing 3,13-dimaleimido DDSQ incorporation. Owing to the formation of crosslinked structures, the DAPU-DDSQs displayed excellent shape memory properties. More importantly, the DAPU-DDSQs displayed the reprocessing (or recycling) properties at the temperature of retro DA reaction. The reprocessing properties of the DAPU-DDSQs can be utilized to re-edit the original shapes of shape memory PUs. Organic-inorganic polyurethane was crosslinked with a difunctional polyhedral oligomeric silsesquioxanes (POSS) via Diels-Alder (DA) reaction. The materials simultaneously had shape memory and reprocessing properties▪. •Organic-inorganic polyurethanes were crosslinked with POSS via Diels-Alder reaction.•The organic-inorganic polyurethanes displayed microphase-separated morphologies.•The POSS-crosslinked polyurethanes had shape memory and reprocessing (or recycling) properties.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2021.124042</doi><orcidid>https://orcid.org/0000-0003-2003-8754</orcidid></addata></record>
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subjects Adducts
Cages
Condensation polymerization
Crosslinking
Diels-Alder reactions
Diphenyl methane diisocyanate
Polyhedral oligomeric silsesquioxane
Polyurethane
Polyurethane resins
POSS
Reprocessing
Reprocessing properties
Shape memory
Shape memory properties
Thermomechanical properties
Thermosetting resins
title Shape recovery and reprocessable polyurethanes crosslinked with double decker silsesquioxane via Diels-Alder reaction
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