A review of cellulose-based catechol-containing functional materials for advanced applications.

With the increment in global energy consumption and severe environmental pollution, it is urgently needed to explore green and sustainable materials. Inspired by nature, catechol groups in mussel adhesion proteins have been successively understood and utilized as novel biomimetic materials. In parallel, cellulose presents a wide class of functional materials rating from macro-scale to nano-scale components. The cross-over among both research fields alters the introduction of impressive materials with potential engineering properties, where catechol-containing materials supply a general stage for the functionalization of cellulose or cellulose derivatives. In this review, the role of catechol groups in the modification of cellulose and cellulose derivatives is discussed. A broad variety of advanced applications of cellulose-based catechol-containing materials, including adhesives, hydrogels, aerogels, membranes, textiles, pulp and papermaking, composites, are presented. Furthermore, some critical remaining challenges and opportunities are studied to mount the way toward the rational purpose and applications of cellulose-based catechol-containing materials.

Biocompatible, Injectable, and Self-Healing Poly(N-vinylpyrrolidone)/Carboxymethyl Cellulose Hydrogel for Drug Release.

Hydrogels have drawn intensive attention as fascinating materials for biomedicine. However, fabricating hydrogels with injectable and self-healing properties remains a challenge. Herein, we reported a biocompatible poly(N-vinylpyrrolidone)/carboxymethyl cellulose (PVP/CMC) hydrogel with excellent injectable and self-healing properties. The PVP/CMC hydrogel exhibits good biocompatible, injectable, and self-healing properties. The sol-gel transition of PVP/CMC hydrogels demonstrates an outstanding self-healing behavior, and the bisected hydrogels can self-heal within 30 s. The hydrogels have a good swelling ratio, and the swelling ratio increases with increasing amount of CMC in PVP and reaches a maximum of 2850% at a 1.0:1.5 PVP and CMC ratio. In addition, the hydrogel possesses excellent drug release capacity, and its drug release rate reaches 70%. Moreover, the release of 4-aminosalicylic acid (4-ASA) in the hydrogel can be controlled by adjusting the proportion of the hydrogel. The PVP/CMC hydrogel with excellent biocompatible, injectable, and self-healing properties has great potential for applications in drug release.

Development of Biocompatible Mussel-Inspired Cellulose-Based Underwater Adhesives.

Conventional adhesives have poor underwater adhesion and harm to human health and the environment during their use, which largely limits their practical applications. Herein, we synthesized cellulose-based adhesives with underwater adhesion and biocompatibility by grafting N-(3,4-dihydroxyphenethyl)methacrylamide into the cellulose chain via atom transfer radical polymerization (ATRP). FTIR, 1H NMR, and XPS analyses ensured the successful preparation of the cellulose-based adhesive polymers. The different properties of the prepared adhesives, including swelling ratio, adhesion strength, and biocompatibility are examined. Results found that the lap shear strength is enhanced by increasing the catechol content. When catechol content is 27.2 mol %, cellulose-based adhesive with the addition of Fe3+ possesses a strong lap shear strength of 2.13 MPa in a dry environment, 0.10 MPa underwater, and 0.16 MPa under seawater for iron substrate, respectively. In addition, the cell culture test demonstrated that the prepared adhesives have outstanding biocompatibility. The cellulose-based adhesives with underwater adhesion and biocompatibility have potential applications in biomedicine, electronic engineering, and construction fields.

Recent advances in TEMPO-oxidized cellulose nanofibers: Oxidation mechanism, characterization, properties and applications.

Cellulose is the richest renewable polymer source on the earth. TEMPO-mediated oxidized cellulose nanofibers are deduced from enormously available wood biomass and functionalized with carboxyl groups. The preparation procedure of TOCNFs is more environmentally friendly compared to other cellulose, for example, MFC and CNCs. Due to the presence of functional carboxyl groups, TOCNF-based materials have been studied widely in different fields, including biomedicine, wastewater treatment, bioelectronics and others. In this review, the TEMPO oxidation mechanism, the properties and applications of TOCNFs are elaborated. Most importantly, the recent advanced applications and the beneficial role of TOCNFs in the various abovementioned fields are discussed. Furthermore, the performances and research progress on the fabrication of TOCNFs are summarized. It is expected that this timely review will help further research on the invention of novel material from TOCNFs and its applications in different advanced fields, including biomedicine, bioelectronics, wastewater treatment, and the energy sector.

Porous Scaffolds Based on Polydopamine/Chondroitin Sulfate/Polyvinyl Alcohol Composite Hydrogels.

In this paper, porous scaffolds based on composite hydrogels were fabricated using polydopamine (PDA), chondroitin sulfate (CS), and polyvinyl alcohol (PVA) via the freezing/thawing method. Different characteristics of the prepared composite hydrogels, including the pore sizes, compression strength, lap shear strength, mass loss, and cytocompatibility were investigated. Scanning electron microscope images (SEM) displayed the hydrogel pore sizes, ranging from 20 to 100 µm. The composite hydrogel exhibited excellent porosity of 95.1%, compression strength of 5.2 MPa, lap shear strength of 21 kPa on porcine skin, and mass loss of 16.0%. In addition, the composite hydrogel possessed good relative cell activity of 97%. The PDA/CS/PVA hydrogel is cytocompatible as a starting point, and it can be further investigated in tissue engineering.

Electrospun chitosan nanofiber constructing superhigh-water-flux forward osmosis membrane.

Forward osmosis (FO) technology exhibits great potential in seawater desalination and wastewater treatment due to its negligible energy consumption and high antifouling, however, the weak desalination capability, especially low water flux, remains challenging. Herein, a cost-effective and high-desalination-performance chitosan (CS)-based FO membrane is developed via coupling the electrospinning CS nanofibers and interfacial-polymerized polyamide (PA). The electrospun nanofibers construct the porous and hydrophilic CS layer with the large pore-diameter of ~274 nm and low thickness of ~10 µm, enabling the effective transport of water molecules, specifically, a superhigh water flux of 107.53 LMH at a low salt-water ratio of 0.24 g·L-1. In addition, such superior desalination performance of the as-prepared FO membrane is universal for the various salt species and concentrations. Our CS nanofiber-based membrane with the high separation capability of water-salt, desirable antibacterial activity, as well as the low cost, offers a roadmap toward the sustainable membrane materials.

Engineered Janus cellulose membrane with the asymmetric-pore structure for the superhigh-water flux desalination.

Membranes are the dominant material for seawater desalination and clean-water harvesting, which are commonly composed of synthetic polymers, showing low hydrophilicity and environmental hazard. Herein, we developed a low-cost, intrinsically green, superhigh-water flux Janus cellulose membrane (CEM) via a facile cellulase etching strategy. Coating cellulase on the single surface of cellulose membrane (such as top surface), triggers effective etching on its top section rather than bottom section, which architects an asymmetric-pore structure of the Janus CEM including porous top-and dense bottom-layer. Such distinction endows the Janus CEM with an unprecedented high-water flux of 135.75 LMH and a low salt-water ratio of 0.29 g·L-1 for 1 M NaCl solution, which is 17-time higher and 62-time lower than that of the pristine CEM. Our Janus CEM enables a promising participant for the advanced membrane materials toward versatile separation engineering.