513
Views
17
CrossRef citations to date
0
Altmetric
Articles

Mechanically strong and pH-responsive carboxymethyl chitosan/graphene oxide/polyacrylamide nanocomposite hydrogels with fast recoverability

, , , , &
Pages 1899-1917 | Received 13 Apr 2017, Accepted 12 Jul 2017, Published online: 28 Jul 2017
 

Abstract

The biocompatible, quickly recoverable, mechanically strong and tough polymer hydrogels have great potential for biomedical applications. A novel carboxymethyl chitosan (CMCTs)/graphene oxide (GO)/polyacrylamide (PAM) nanocomposite (NC) hydrogel with excellent mechanical performance was synthesized through a facile, one-pot free radical polymerization, using GO nanosheets as the crosslink centers instead of toxic organic molecules. The content of GO nanosheets and CMCTs has great influence on the mechanical properties of CMCTs/GO/PAM NC hydrogels. When the amount of GO nanosheets is 0.118 wt % and CMCTs is 1.5 wt % (to the total weight of CMCTs and acrylamide), CMCTs/GO/PAM hydrogel displays a compressive stress as high as 5.8 MPa at the breaking deformation of 87.5% and a tensile strength of 223.6 kPa at the failure strain of 631%. Besides, with nearly complete recovery in 1 min at the room temperature after unloading, the CMCTs/GO/PAM hydrogels exhibit excellent fast recoverability. Additionally, the CMCTs/GO/PAM hydrogels also have an obvious pH-responsive property.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.