Large‐Sized Hydrogel Sheet Incorporated with Dual Physical Crosslinkers for Enhanced Mechanical and Adhesive Properties

Author:

Nam Kibeom1,Park Ju Hyang2,Kim Eon Ji1,Kim Jong Ryeol1,Min Yuho3,Hyun Dong Choon1,Lee Dong Yun1ORCID

Affiliation:

1. Department of Polymer Science and Engineering Kyungpook National University Daegu 41566 South Korea

2. Korea Textile Development Institute Daegu 41842 South Korea

3. School of Materials Science and Engineering Kyungpook National University Daegu 41566 South Korea

Abstract

AbstractThis work reports the fabrication of a large‐sized hydrogel sheet with enhanced mechanical and adhesive properties. The fabrication involves the introduction of carboxymethyl‐modified cellulose nanofibers (m‐CNFs) and solid silica nanoparticles (SSNs) as physical cross‐linkers into acrylic acid monomer (AA), followed by bar coating and photopolymerization. The addition of the nanomaterials to the monomer solution renders it viscous, enabling the fabrication of A4‐sized hydrogel sheets with uniform thickness and enhanced mechanical and adhesive properties. Interestingly, the combined incorporation of both the nanomaterials generates a synergistic effect to improve the properties much more, which results from the hierarchical rupture of the multiple hydrogen‐bonded interactions among the poly(acrylic acid) (PAA) matrix, m‐CNFs, and SSNs. Under optimal conditions, the hydrogel sheet incorporated with the dual crosslinkers exhibits a sevenfold higher toughness and a sixfold increased peel strength than plain PAA, together with good biocompatibility. Furthermore, when mesoporous silica nanoparticles (MSNs) with active agent loading into their pores are incorporated instead of SSNs, the active agent can be released from the hydrogel sheet in a sustained or temperature‐sensitive manner, indicating that the system is potentially applicable to transdermal drug delivery system with no additional adhesive.

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials

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