Hydrolytic degradation of ROMP thermosetting materials catalysed by bio-derived acids and enzymes: from networks to linear materials

This paper reports the first example of degradable ROMP thermosetting materials catalysed by bio-derived acids and cutinase from Thermobifida cellulosilytica (Thc_Cut1). The ROMP thermosetting materials are based on norbornene dicarboximides containing acetal ester groups only in the crosslinking mo...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2016, Vol.18 (19), p.519-5199
Hauptverfasser: Hou, S, Hoyle, D. M, Blackwell, C. J, Haernvall, K, Perz, V, Guebitz, G. M, Khosravi, E
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container_issue 19
container_start_page 519
container_title Green chemistry : an international journal and green chemistry resource : GC
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creator Hou, S
Hoyle, D. M
Blackwell, C. J
Haernvall, K
Perz, V
Guebitz, G. M
Khosravi, E
description This paper reports the first example of degradable ROMP thermosetting materials catalysed by bio-derived acids and cutinase from Thermobifida cellulosilytica (Thc_Cut1). The ROMP thermosetting materials are based on norbornene dicarboximides containing acetal ester groups only in the crosslinking moiety. The insoluble cross-linked materials were subjected to acid-catalysed hydrolysis using bio-derived acetic and citric acids as well as enzymatic degradation using Thc_Cut1, resulting in the materials becoming completely soluble in dichloromethane. 1 H NMR and rheological analysis performed on materials after acid-catalysed hydrolysis showed characteristics indistinguishable to those of the linear polymer analogues. These analyses confirmed the cleavage of the crosslinking moiety upon degradation with the main backbone chains remaining intact. The glass transition temperatures of the polymer materials after acid-catalysed hydrolysis were the same as those observed for the linear polymer analogues. TGA showed that the cross-linked polymers were thermally stable to 150 °C, beyond which they showed weight losses due to the thermal cleavage of the acetal ester linkages. ROMP thermosetting polymers are degraded by bio-derived acetic and citric acids as well as cutinase from Thermobifida cellulosilytica enzyme becoming soluble in DCM. The degradation process breaks the acetal ester linkages allowing transition to linear thermoplastic polymers.
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These analyses confirmed the cleavage of the crosslinking moiety upon degradation with the main backbone chains remaining intact. The glass transition temperatures of the polymer materials after acid-catalysed hydrolysis were the same as those observed for the linear polymer analogues. TGA showed that the cross-linked polymers were thermally stable to 150 °C, beyond which they showed weight losses due to the thermal cleavage of the acetal ester linkages. ROMP thermosetting polymers are degraded by bio-derived acetic and citric acids as well as cutinase from Thermobifida cellulosilytica enzyme becoming soluble in DCM. 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The insoluble cross-linked materials were subjected to acid-catalysed hydrolysis using bio-derived acetic and citric acids as well as enzymatic degradation using Thc_Cut1, resulting in the materials becoming completely soluble in dichloromethane. 1 H NMR and rheological analysis performed on materials after acid-catalysed hydrolysis showed characteristics indistinguishable to those of the linear polymer analogues. These analyses confirmed the cleavage of the crosslinking moiety upon degradation with the main backbone chains remaining intact. The glass transition temperatures of the polymer materials after acid-catalysed hydrolysis were the same as those observed for the linear polymer analogues. TGA showed that the cross-linked polymers were thermally stable to 150 °C, beyond which they showed weight losses due to the thermal cleavage of the acetal ester linkages. 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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Citric acid
Cleavage
Crosslinking
Degradation
Esters
Glass transition temperature
Hydrolysis
Networks
title Hydrolytic degradation of ROMP thermosetting materials catalysed by bio-derived acids and enzymes: from networks to linear materials
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