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Herein, we reported a general and green synthetic strategy for photochromic functional alginate derivatives grafting with isoindolinone spiroxanthenes. Under mild condition, diverse 2-aminoalkyl isoindolinone spiroxanthene derivatives have been prepared from organic photochromic isobenzofuranone spiroxanthenes (including rhodamine B, rhodamine 6G and fluorescein), and grafted on alginate chains through amidation reaction using diamine as a linkage with water as a green solvent at room temperature. The photochromic properties of the fluorophores-modified polymers and the effect of pH value have been explored. Under acid conditions, the spiroisoindolinone rings of alginate derivatives are opened resulting in showing absorption bands and fluorescence with orange to green emission, while the alginate derivatives turned to colourless under basic conditions which is reversibly. In addition to biodegradability and biocompatibility, the polymers exhibit good film-forming properties simultaneously. The films and fibers produced from the alginate derivatives also project good fluorescence properties.

RESUMEN

Lightweight, flame retardant biomass aerogels combining with multi-functionalities are promising for thermal insulation, noise absorption and smart sensors. However, high flammability hinders the application of these aerogels in extreme condition. Herein, lightweight, flame retardant aerogel with fire-warning properties fabricated from resource-abundant graphite and green carboxymethyl cellulose (CMC) is reported. During sonicating expandable graphite (EG) in CMC solution, CMC not only fabricates the downsizing process via hydrogen bonding effect but also forms stable dispersions. Then biomass aerogel is fabricated by freeze-drying strategy and enhanced by metal ionic cross-linking method. This aerogel demonstrates Janus properties for electrical conductivity and thermal conductivity. Due to the synergistic flame retardant effect of graphite nanocomposite and metal ions with a barrier effect and catalytic carbonization capacity, the flame retardancy of these aerogels are enhanced with fire-warning properties. Furthermore, these aerogels are used for monitoring physical deformations as smart sensors, which provides inspiration and a sustainable solution for developing low-cost biomass aerogel with multifunction.

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Nanocomposite conductive fibers are of great significance in applications of wearable devices, smart textiles, and flexible electronics. Integration of conductive nanomaterials into flexible bio-based fibers with multifunctionality remains challenging due to interface failure, poor flexibility, and inflammability. Although having broader applications in textiles, regenerated cellulose fibers (RCFs) cannot meet the requirements of wearable electronics owing to their intrinsic insulation. In this study, we constructed conductive RCFs fabricated by coordinating copper ions with cellulose and reducing them into stable Cu nanoparticles coated on their surface. The Cu sheath offered excellent electrical conductivity (4.6 × 105 S m-1), electromagnetic interference shielding, and enhanced flame retardance. Inspired by plant tendrils, the conductive RCF was wrapped around an elastic rod to develop wearable sensors for human health and motion monitoring. The resultant fibers not only form stable conductive nanocomposites on the fiber surface by chemical bonds but also exhibit a huge potential for wearable devices, smart sensors, and flame-retardant circuits.

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TEMPO oxidized nano-fibrillated cellulose (TONFC) has been used in different applications including biomedical, packing materials, paints and cosmetics because of its higher transparency, mechanical properties and better biocompatibility. However, pulping is always required to remove lignin and hemicellulose, and high-energy homogenization is required to defibrillate cellulose bundle into filament. Therefore, it is desirable to find a novel way to get TONFC with high carboxyl content without intensive mechanical disintegration. In this work, nanocellulose (TOHOLO) with higher carboxyl groups (2.2 ± 0.2 mmol/g) and smaller size (length = 400-685 nm and diameter = 5.9 nm) was prepared by a two-step strategy without intensive mechanical homogenization. In addition to the advantages in terms of diameter and carboxyl groups, TOHOLO showed better transparency and re-dispersibility as well as higher mechanical properties (122.8 MPa) compared to previous reports. Furthermore, for high carboxyl group and dispersibility, the TOHOLO can be used as a reinforcing filler to fabricate nanocomposites. The reinforced PVA fibers show a tensile strength of 484.4 MPa, which is about 170 % higher than comparison samples (PVA/TOCN-M, 291.9 MPa).

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Green and scalable production of some fibrous materials with higher fracture energy has long been the goal of researchers. Although some progress has been made in recent years in the research of materials with high fracture energy, inspired by the fiber structure of spider silk, it is still a great challenge to produce artificial fibers with extremely high toughness using a simple and green process. Here, we use the molecular and nanoscale engineering of calcium phosphate oligomers (CaP, < 1 nm) and waterborne polyurethanes (WPU) macromolecules that have strong interactions to form organic-inorganic networks just like ß-sheet crystalline and flexible amorphous regions in spider silk. Through a simple and green route based on widespread paper string processing techniques, we fabricate a strong and supertough bioinspired fiber with a high strength (442 MPa), which is 7-15 times higher than the strength of counterpart PU (20-30 MPa), and a super toughness (640 MJ m-3), which is 2-3.5 times higher than the toughness of spider dragline silk. This technique provides a strategy for industrially manufacturing spider fiber-like artificial fibers with a super toughness.

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RESUMEN

The nanostructured metal sulfides have been reported as promising anode materials for sodium-ion batteries (SIBs) due to their high theoretical capacities but have suffered from the unsatisfactory electronic conductivity and poor structural stability during a charge/discharge process, thus limiting their applications. Herein, the one-dimensional (1D) porous FeS/carbon fibers (FeS/CFs) micro/nanostructures are fabricated through facile pyrolysis of double-helix-structured Fe-carrageenan fibers. The FeS nanoparticles are in situ formed by interacting with sulfur-containing group of natural material ι-carrageenan and uniformly embedded in the unique 1D porous carbon fibrous matrix, significantly enhancing the sodium-ion storage performance. The obtained FeS/CFs with optimized sodium storage performance benefits from the appropriate carbon content (20.9 wt %). The composite exhibits high capacity and excellent cycling stability (283 mAh g-1 at current density of 1 A g-1 after 400 cycles) and rate performance (247 mAh g-1 at 5 A g-1). This work provides a simple strategy to construct 1D porous FeS/CFs micro/nanostructures as high-performance anode materials for SIBs via a unique sustainable and environmentally friendly way.