Interfacial assembly of self-healing and mechanically stable hydrogels for degradation of organic dyes in water

Guihua Yan,Huiqiang Wang,Xing Tang,Xianhai Zeng,Wenjing Hong,Lu Lin,Yunchao Feng,Yong Sun

doi:10.1038/s43246-020-0043-0

Guihua Yan, Huiqiang Wang + Show 6 more

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https://doi.org/10.1038/s43246-020-0043-0

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Mussel-inspired hydrogels have gained attention for underwater applications, including treatment of wastewater. However, they are typically limited by poor mechanical properties, short-term mechanical stability and by not being reusable. Here, we develop a mechanically stable and self-healing hydrogel with high mechanical strength for the degradation of dyes in wastewater, based on cellulose-derived co-polydopamine@Pd nanoparticles. A dynamic catechol redox system was achieved by reversible conversion between semiquinone and quinone/hydroquinone radicals, endowing the hydrogel with stable mechanical properties and self-healing behavior. Furthermore, a graphene oxide membrane is covalently grafted on to the hydrogel surface, which regulates its water permeability and intercepts some metal ions or large particles, protecting the hydrogel structure. High catalytic activity for anionic and cationic dyes is achieved, with the degradation rate reaching more than 95% after multiple cycles without significant deterioration in performance or hydrogel structure. Our work demonstrates a route to achieve mechanically stable hydrogels for degradation of organic dyes in wastewater.

Highlights

Mussel-inspired hydrogels have gained attention for underwater applications, including treatment of wastewater
Previous reports suggested that an effective combination of the catalytic performance, longterm mechanical property, and selective permeation would benefit from an integrative strategy
This hydrogel is constructed by grafted polymers, that is, coagulating them from an aqueous precursor solution containing cellulose–graft–polydopamine loaded with Pd NPs (DACOPDA@Pd NPs), acrylic acid (AA), and sodium alginate (SA)

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Introduction

Mussel-inspired hydrogels have gained attention for underwater applications, including treatment of wastewater. SA and AA are mixed with the undried DACO-PDA@Pd NPs to construct a catechol-conjugated alginate hydrogel with high toughness owing to the quinone–catechol-reversible reaction under an ambient environment (Fig. 2b, c). The introduction of multifunctional groups and the successful loading of Pd NPs on the surface of the DACO-PDA were essential to the construction of hydrogel network structure.

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