Analysis of the Effect of Processing Conditions on Physical Properties of Thermally Set Cellulose Hydrogels.

cellulose chemical cross-linking hydrogel physical cross-linking

Journal

Materials (Basel, Switzerland)
ISSN: 1996-1944
Titre abrégé: Materials (Basel)
Pays: Switzerland
ID NLM: 101555929

Informations de publication

Date de publication:
01 Apr 2019
Historique:
received: 05 03 2019
revised: 24 03 2019
accepted: 28 03 2019
entrez: 4 4 2019
pubmed: 4 4 2019
medline: 4 4 2019
Statut: epublish

Résumé

Cellulose-based hydrogels were prepared by dissolving cellulose in aqueous sodium hydroxide (NaOH)/urea solutions and casting it into complex shapes by the use of sacrificial templates followed by thermal gelation of the solution. Both the gelling temperatures used (40⁻80 °C), as well as the method of heating by either induction in the form of a water bath and hot press or radiation by microwaves could be shown to have a significant effect on the compressive strength and modulus of the prepared hydrogels. Lower gelling temperatures and shorter heating times were found to result in stronger and stiffer gels. Both the effect of physical cross-linking via the introduction of additional non-dissolving cellulosic material, as well as chemical cross-linking by the introduction of epichlorohydrin (ECH), and a combination of both applied during the gelation process could be shown to affect both the mechanical properties and microstructure of the hydrogels. The added cellulose acts as a physical-cross-linking agent strengthening the hydrogen-bond network as well as a reinforcing phase improving the mechanical properties. However, chemical cross-linking of an unreinforced gel leads to unfavourable bonding and cellulose network formation, resulting in drastically increased pore sizes and reduced mechanical properties. In both cases, chemical cross-linking leads to larger internal pores.

Identifiants

pubmed: 30939751
pii: ma12071066
doi: 10.3390/ma12071066
pmc: PMC6479291
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Ministry of Business, Innovation and Employment
ID : UOCX1304

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Auteurs

Tim Huber (T)

Department of Chemical and Process Engineering and Biomolecular Interaction Centre, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand. tim.huber@canterbury.ac.nz.
School of Product Design, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand. tim.huber@canterbury.ac.nz.

Sean Feast (S)

Department of Chemical and Process Engineering and Biomolecular Interaction Centre, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand. sean.feast@pg.canterbury.ac.nz.

Simone Dimartino (S)

Department of Chemical and Process Engineering and Biomolecular Interaction Centre, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand. simone.dimartino@ed.ac.uk.
Institute for Bioengineering, School of Engineering, University of Edinburgh, Edinburgh EH9 3FB, UK. simone.dimartino@ed.ac.uk.

Wanwen Cen (W)

Graymont Limited, New Zealand Region Office and Otorohanga Plant, 498 Old Te Kuiti Road RD 6, Otorohanga 3900, New Zealand. wcen603@aucklanduni.ac.nz.

Conan Fee (C)

Department of Chemical and Process Engineering and Biomolecular Interaction Centre, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand. conan.fee@canterbury.ac.nz.
School of Product Design, University of Canterbury, Private Bag 4800, Christchurch 8020, New Zealand. conan.fee@canterbury.ac.nz.

Classifications MeSH