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      One-pot cellulose etherification and self-crosslinking via a mild hydroxyl–yne click reaction in a homogeneous system

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          Abstract

          The one-pot etherification and crosslinking of cellulose were successfully achieved by a hydroxyl–yne click reaction in a homogeneous system at room temperature.

          Abstract

          The chemical modification of cellulose via sustainable pathways is highly desirable for high performance cellulose derivatives. Herein, a novel one-pot method for the etherification and self-crosslinking of cellulose is demonstrated, for the first time, by applying the mild hydroxyl–yne click reaction that occurs in a homogeneous system. Besides the benzene rings and carbonyl groups, the conjugated CC double bonds formed by the hydroxyl–yne click reaction were also introduced to the resulting cellulose phenyl propylene ketone ethers (CPPKs). Interestingly, the conjugated CC double bonds in CPPKs could crosslink via photo-dimerization reactions during the etherification of cellulose, forming chemically crosslinked CPPKs. Therefore, the CPPK films exhibited excellent mechanical properties and solvent resistance. The ultimate strength of CPPKs was 85.7 ± 1.5 MPa, 1.6 times higher than that of raw cellulose. Moreover, the CPPK films were stable in high-polarity solvents (DMSO, DMAc, and DMF) for 6 months. Furthermore, CPPKs not only exhibited excellent UV-shielding properties but also showed good UV self-reinforcing properties; both CPPK hydrogels and films displayed improved mechanical properties under UV irradiation. This work provides a sustainable one-pot method for etherification and self-crosslinking of cellulose in the homogeneous system, which imparts excellent stress, solvent resistance, UV-shielding, and UV self-reinforcement to cellulose, promoting high-value utilization of cellulose materials.

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          High-throughput screening for ionic liquids dissolving (ligno-)cellulose.

          The recalcitrance of lignocellulosic biomass poses a major challenge for its sustainable and cost-effective utilization. Therefore, an efficient pretreatment is decisive for processes based on lignocellulose. A green and energy-efficient pretreatment could be the dissolution of lignocellulose in ionic liquids. Several ionic liquids were identified earlier which are capable to dissolve (ligno-)cellulose. However, due to their multitude and high costs, a high-throughput screening on small scale is essential for the determination of the most efficient ionic liquid. In this contribution two high-throughput systems are presented based on extinction or scattered light measurements. Quasi-continuous dissolution profiles allow a direct comparison of up to 96 ionic liquids per experiment in terms of their dissolution kinetics. The screening results indicate that among the ionic liquids tested EMIM Ac is the most efficient for dissolving cellulose. Moreover, it was observed that AMIM Cl is the most effective ionic liquid for dissolving wood chips.
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            Biopolymer nanofibrils: Structure, modeling, preparation, and applications

            Biopolymer nanofibrils exhibit exceptional mechanical properties with a unique combination of strength and toughness, while also presenting biological functions that interact with the surrounding environment. These features of biopolymer nanofibrils profit from their hierarchical structures that spun angstrom to hundreds of nanometer scales. To maintain these unique structural features and to directly utilize these natural supramolecular assemblies, a variety of new methods have been developed to produce biopolymer nanofibrils. In particular, cellulose nanofibrils (CNFs), chitin nanofibrils (ChNFs), silk nanofibrils (SNFs) and collagen nanofibrils (CoNFs), as the four most abundant biopolymer nanofibrils on earth, have been the focus of research in recent years due to their renewable features, wide availability, low-cost, biocompatibility, and biodegradability. A series of top-down and bottom-up strategies have been accessed to exfoliate and regenerate these nanofibrils for versatile advanced applications. In this review, we first summarize the structures of biopolymer nanofibrils in nature and outline their related computational models with the aim of disclosing fundamental structure-property relationships in biological materials. Then, we discuss the underlying methods used for the preparation of CNFs, ChNFs, SNF and CoNFs, and discuss emerging applications for these biopolymer nanofibrils.
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              Cellulose-Lignin Biodegradable and Flexible UV Protection Film

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                Author and article information

                Contributors
                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                April 03 2023
                2023
                : 25
                : 7
                : 2608-2619
                Affiliations
                [1 ]Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Jiangsu Key Lab of Biomass-Based Green Fuel and Chemicals, Key Laboratory of Forestry Genetics and Biotechnology of Ministry of Education, College of Chemical Engineering, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China
                [2 ]State Key Laboratory of New Textile Materials and Advanced Processing Technologies, Wuhan Textile University, Wuhan 430200, China
                Article
                10.1039/D2GC04278A
                b2953099-aec2-4dd2-8433-2c98785ce6f0
                © 2023

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

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