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      Super-strong and tough poly(vinyl alcohol)/poly(acrylic acid) hydrogels reinforced by hydrogen bonding

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          Abstract

          Super-strong and tough poly(vinyl alcohol)/poly(acrylic acid) hydrogels based on hydrogen bonding are prepared by the strategy of immersing and cold-drawing.

          Abstract

          Synthetic hydrogels or water-containing polymeric materials are much inferior to biological tissues and solid plastics in many aspects of mechanical properties; it is a great challenge to develop hydrogels with mechanical properties comparable with or even superior to those of biological tissues and plastics. Here, we report a type of super-strong and tough hydrogen-bonded poly(vinyl alcohol)/poly(acrylic acid) (PVA/PAA) hydrogel by immersing as-prepared PVA hydrogels in aqueous PAA solutions and then cold-drawing the hydrogels to different strains. The immersing process introduces PAA chains into the PVA hydrogels, which increases the cross-linking density by hydrogen bonding and hence, much improved mechanical properties and low water contents (35.9–40.2 wt%) are observed. The cold-drawing orients the polymer chains, which enables the formation of more and stronger hydrogen bonds. The mechanical properties of cold-drawn gels are dramatically enhanced, with tensile strength and elastic modulus up to 140 and 100 MPa, respectively; also, super-high toughness (117 MJ m −3) and fracture energy (101 kJ m −2) are obtained. Very impressively, the ultra-high tensile strengths of the cold-drawn hydrogels are superior to those of biological tissues and most solid engineered plastics. Characterizations and comparative studies prove that the enhancement of mechanical properties is mainly due to the formation of more hydrogen bonding rather than the loss of water or the change in crystallinity. This study provides a new strategy for preparing super-strong physically cross-linked hydrogels and other polymeric materials. This super-strong and tough hydrogel may find potential applications in biomedical and load-bearing fields.

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          Most cited references51

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          Highly stretchable and tough hydrogels.

          Hydrogels are used as scaffolds for tissue engineering, vehicles for drug delivery, actuators for optics and fluidics, and model extracellular matrices for biological studies. The scope of hydrogel applications, however, is often severely limited by their mechanical behaviour. Most hydrogels do not exhibit high stretchability; for example, an alginate hydrogel ruptures when stretched to about 1.2 times its original length. Some synthetic elastic hydrogels have achieved stretches in the range 10-20, but these values are markedly reduced in samples containing notches. Most hydrogels are brittle, with fracture energies of about 10 J m(-2) (ref. 8), as compared with ∼1,000 J m(-2) for cartilage and ∼10,000 J m(-2) for natural rubbers. Intense efforts are devoted to synthesizing hydrogels with improved mechanical properties; certain synthetic gels have reached fracture energies of 100-1,000 J m(-2) (refs 11, 14, 17). Here we report the synthesis of hydrogels from polymers forming ionically and covalently crosslinked networks. Although such gels contain ∼90% water, they can be stretched beyond 20 times their initial length, and have fracture energies of ∼9,000 J m(-2). Even for samples containing notches, a stretch of 17 is demonstrated. We attribute the gels' toughness to the synergy of two mechanisms: crack bridging by the network of covalent crosslinks, and hysteresis by unzipping the network of ionic crosslinks. Furthermore, the network of covalent crosslinks preserves the memory of the initial state, so that much of the large deformation is removed on unloading. The unzipped ionic crosslinks cause internal damage, which heals by re-zipping. These gels may serve as model systems to explore mechanisms of deformation and energy dissipation, and expand the scope of hydrogel applications.
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            Nanocomposite Hydrogels: A Unique Organic–Inorganic Network Structure with Extraordinary Mechanical, Optical, and Swelling/De-swelling Properties

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              The Polyrotaxane Gel: A Topological Gel by Figure-of-Eight Cross-links

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                JMCBDV
                Journal of Materials Chemistry B
                J. Mater. Chem. B
                Royal Society of Chemistry (RSC)
                2050-750X
                2050-7518
                December 12 2018
                2018
                : 6
                : 48
                : 8105-8114
                Affiliations
                [1 ]Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University
                [2 ]Beijing 100875
                [3 ]P. R. China
                [4 ]State Key Laboratory of Polymer Physics and Chemistry, Joint Laboratory of Polymer Science and Material, Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences
                [5 ]Beijing 100190
                Article
                10.1039/C8TB02556H
                32254930
                e3cd891e-04f0-41a0-8532-f2eca424ae35
                © 2018

                http://rsc.li/journals-terms-of-use

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