Development of polyvinyl alcohol/carrageenan hydrogels and fibers via KOH treatment for Morse code information transmission.

To solve the inherent problems of conductive hydrogels, such as relatively low mechanical properties and fatigue resistance, inability to work after water loss, and difficulty weaving. In this study, the borax-crosslinked polyvinyl alcohol/k-carrageenan (kC) conducting hydrogels (BPKKOH) were prepared by a simple one-pot method, and KOH treatment was used instead of the cumbersome and time-consuming freeze-thaw cycle to improve the comprehensive properties. The KOH treatment increased the hydrogel hydrogen bonding content by 7.72 % and synergized with the induction of kC by K+ to enhance the tensile and compressive strengths by 8.12 and 34.6 times, respectively. Meanwhile, the BPKKOH hydrogel's fatigue resistance and shape recovery after water loss were improved. Additionally, the BPKKOH hydrogels can be monitored for finger bending, showing clear and stable differences in electrical signals. BPKKOH hydrogels combined with Morse code realize applications in information transmission and encryption/decryption. Notably, introducing KOH ensures the molding and preparation of BPKKOH hydrogel fibers while having good signal responsiveness and monitoring ability. More importantly, it can be woven into fabrics that can be loaded with heavy weights, which has the potential to be directly applied in smart wearables. This work provides new ideas for applying flexible sensors and wearable smart textiles.

Robust Superhydrophobic Composite Fabric with Self-Healing and Chemical Durability.

Superhydrophobic fabrics with multiple functions have become a research hotspot. However, it is challenging to make self-healing mechanically robust and eco-friendly superhydrophobic fabrics, which are limited by complex fabrication processes and excessive use of environmentally unfriendly solvents during fabrication. Herein, inspired by the secretion of a waxy substance from the surface of lotus leaves to restore water repellency, self-healing superhydrophobic composite fabrics (as-synthesized PA66/6-PET@Tico) are obtained by constructing a papillary TiO2 and tentacle-like fluorinated acrylate polymer (FCB015) coating on polyester-nylon composite fabrics using two-step hydrothermal method. The result indicates that PA66/6-PET@Tico with hierarchical micro/nanostructure exhibits excellent superhydrophobic and self-healing properties. Compared with FCB015 coated fabric, the contact angles (CA) of water and soybean oil rise to 172.2° and 166.8° from 137.4° and 98.8°, respectively. After mechanical abrasion, PA66/6-PET@Tico recovers a water contact angle (WCA) of 165.6° at room temperature. The WCA remains higher than 155° after 18 h of chemical corrosion. Furthermore, the bacterial inhibition rates of PA66/6-PET@Tico for Staphylococcus Aureus and Escherichia Coli are 99.90 and 98.38%, respectively. In this work, a new idea is proposed for designing a simple and effective self-healing superhydrophobic coating, expecting to promote the large-scale industrial production and application of functional surfaces.

Low-temperature superelastic, anisotropic, silane-crosslinked sodium alginate aerogel for thermal insulation.

Bio-aerogels have attracted much attention owing to their remarkable properties, but their brittle and poor elasticity has limited their further applications. Here, we propose a strategy of in-situ silanization crosslinking combined with unidirectional freeze casting (SUFC) to prepare superelastic sodium alginate (SA) aerogels. The resulting aerogel was ultra-light (0.048 g/cm3), high porosity (96.86 %), and self-extinguishing from fire. Aerogels exhibited anisotropic properties, such as low-temperature elasticity (500 g compression at -70 °C 10-cycle, 99.6 % recovery), exceptional fatigue resistance (100-cycle at 50 % strain), and excellent thermal insulation (0.0696 W·m-1·K-1). Thus, the SUFC strategy provides considerable freedom for constructing multi-material, lamellar/honeycomb structured alginate-based aerogels, which pave the way to thermal insulation development at low temperatures.

Bilayer fiber membrane electrospun from polylactic acid/alginate/bromelain and polylactic acid for enhancing the functionality of tea bags.

Tea bags have been extensively used in the food industry and daily life as an efficient way to pack tea. However, the large pores of the commercial tea bags not only lead to the inner contents of tea bag susceptible to bacteria and moisture but also result in the faster water infusion which is undesired during tea brewing. In this study, the polylactic acid (PLA)-PLA/sodium alginate (SA)/bromelain (BL) bilayer fiber membrane imitating the asymmetric wetting structure of lotus leaf blades was fabricated to avoid the above disadvantages of commercial tea bag. The PLA/SA/BL skin-core nanofiber membrane which imitating the skin-core structure of lotus leaf stems was first prepared as the hydrophilic and support layer, then a hydrophobic PLA layer was deposited on top via electrospinning. The PLA-PLA/SA/BL bilayer fiber membrane had a breaking strength of 5.5 MPa and started to decompose at 260 °C. Using this bilayer membrane, tea bags were designed with a novel structure where the hydrophobic PLA layer was placed in the same direction. The novel structure endow the those tea bags a slow and directional water transfer property. Therefore, the PLA-PLA/SA/BL bilayer fiber membrane has great potential for applications as tea bags.

In-situ growth of zinc sulfide on the surface of alginate-based biomass carbon: A new material for removing methylene blue/basic fuchsin and copper ions.

This work aims to prepare a composite adsorbent with a fixed shape to improve the performance of carbon materials and to solve the problem of adsorbent in powder form which is difficult to recycle after use. The BC-ZnS composite system was successfully prepared by hydrothermal method based on the preparation of biomass carbon (BC) using alginate (Alg), while the ZnS component was grown in-situ on the surface of BC. The effects of Alg, Zn source, hydrothermal temperature and time on the synthesis of BC-ZnS were explored, the results indicated that ZnS was successfully grown in-situ on the BC surface, while the BC maintained its original morphology. BC-ZnS showed excellent adsorption capacity for methylene blue (MB), basic fuchsin (BF), and copper ions (Cu2+), reaching 301.50 mg/g for MB and exhibiting good cyclic stability. The adsorption of MB/BF/Cu2+ by BC-ZnS was characterized by the presence of multiple forces, where the BC component mainly depended on the electrostatic force of Alg residue, while the ZnS involves electrostatic forces, ion exchange and Lewis acid/base soft-soft interactions. The adsorption process conforms to pseudo-first-kinetics and is a spontaneous entropy-increasing process. BC-ZnS can be a candidate for reusable wastewater treatment and has excellent potential for application.

Guar-based aerogels with oriented lamellar structure and lightweight properties for flame-retardant and thermal insulation.

In this study, a multi-functional guar gum aerogel with the oriented lamellar structure, which introduced sodium silicate (Na2O·nSiO2) and phytic acid (PA) as thermal insulation additives and flame-retardant agents, respectively, was fabricated via freeze drying. Our aerogel's chemical structure, morphology, and thermal and mechanical properties were analyzed. The oriented lamellar structure was attributed to the orientated growth of ice crystals, which was induced by the "silicate-guar, guar-phytate, and phytate-silicate" multiple hydrogen bonds formed between Na2O·nSiO2, PA, and guar gum. The density of the sample with 2 wt% PA could reach 0.0335 g·cm-3, and the porosity was 5 %, along with a specific pore volume of 0.8144 cm3·g-1. The mechanical properties and thermal insulation performed significant differences in the radial and axial direction of the oriented lamella (nearly 100 % resilience while 50 % deformation quantity and 0.0235 W/(m*K) of thermal conductivity in the radial direction, up to 0.079 MPa of compressive strength in the axial direction). The presence of PA attached a good flame-retardant ability to our aerogel (The Limiting Oxygen Index (LOI) was 30.77 %). This work provides a novel and promising method for developing anisotropic aerogel with excellent potential in building energy efficiency and flame-retardant.

Molybdenum disulfide nanoflowers - doped sodium alginate/polyvinyl alcohol porous xerogel for methylene blue and copper ion adsorption.

In order to improve the adsorption performance of MoS2, as well as to solve the problems of MoS2-powder in adsorption, which is prone to agglomeration and difficulty to be recycled, we prepared MoS2-nanoflowers(MoS2-NFs), and mixed them with sodium alginate/polyvinyl alcohol(SA/PVA) to prepare MoS2-NFs/SA/PVA xerogel(MSP) by freezing-lyophilization. Then two forms of xerogels - block-MSP(MSPB) and spherical-MSP(MSPS) were prepared, and they were used as methylene blue(MB) and Cu2+ adsorbent. It was found that MoS2-NFs were evenly dispersed inside the SA/PVA with no agglomeration, while the interior of MSPB/MSPS showed the structure of parallel-pores and radial-pores, respectively. The adsorption capacity of MSPB/MSPS on MB can reach 233 mg/g, which is five times higher than SA/PVA-gel, showing excellent synergistic-adsorption effect, and the adsorption capacity for Cu2+ reaches 271 mg/g. The adsorption mechanism indicated that the adsorption of MB by MSPB/MSPS conformed to pseudo-first-order model, with electrostatic force as the main force. And their adsorption of Cu2+ conformed to pseudo-second-order model and was dominated by Lewis acid/base soft-soft interactions. Notably, after long-term adsorption, MSPB/MSPS maintains its shape and more than 90 % of the adsorption capacity, ensuring the recovery and reuse of materials. So, MSPB/MSPS has great potential in adsorption, providing a new solution for sewage purification.

Guar gum-based multilayer fiber membranes inspired by plant transpiration for enhancing the functionality of dry facial masks.

As more eco-friendly and economical choice for wet facial masks, dry facial masks have always had the problem of cumbersome application process and poor water retention property. In this study, based on the mechanism of directional water transport of Janus membrane and plant transpiration, the hydrophobic polylactic acid (PLA) nanofiber layer and the superhydrophilic guar gum (GG) nanofiber layer were prepared on both sides of the silk facial mask (SM) by electrospinning to obtain the guar gum-based bionic Janus directional water transport facial mask (G-DFM). The results showed that the directional water transport function improved the facial mask's water retention by 37 %, and the nicotinamide (NAM) encapsulated in the GG layer gave the facial mask excellent whitening and antibacterial properties. The GG layer could be directed to swell after absorbing water to form the "gel-like", which ensured that the G-DFM could continue to release NAM during its work and would enhance the attachment between the G-DFM and the skin. G-DFM not only retained the advantages of SM but also expanded the functions that SM did not have, providing an idea for designing more practical and ideal facial masks in the future.

Dual-stimuli responsive skin-core structural fibers with an in situ crosslinked alginate ester for hydrophobic drug delivery.

To solve the problems of low bioavailability and low intestinal release efficiency of curcumin as a hydrophobic drug in the treatment of diabetes, a novel alginate ester/Antarctic krill protein/2-formylphenylboronic acid (AE/AKP/2-FPBA) skin-core structural fiber with pH and glucose stimulation responsiveness was prepared by an acid-catalyzed polyol in situ crosslinked phase separation method as a drug delivery system. The reaction mechanism and apparent morphology of the fiber were studied. The controlled release ability of the fiber in simulated liquids was evaluated. AE targeted the release of curcumin by pH stimulation; the release amount in the simulated colonic fluid reached 100%, while the release amount in the simulated digestive fluid was less than 12%. 2-FPBA controlled the release rate of curcumin by glucose stimulation, which increases with the increase of 2-FPBA content. Moreover, the cytotoxicity test confirmed that the skin-core structural fiber was non-toxic. These results suggest that skin-core structural fibers have great potential as curcumin delivery systems.

Development of cell adhesive and inherently antibacterial polyvinyl alcohol/polyethylene oxide nanofiber scaffolds via incorporating chitosan for tissue engineering.

Currently, polyvinyl alcohol (PVA) and polyethylene oxide (PEO), as tissue engineering scaffolds materials, had been widely studied, however the hard issues in cell adhesive and antimicrobial properties still seriously limited their application in biomedical respects. Herein, we solved both hard issues by incorporating chitosan (CHI) into the PVA/PEO system, and successfully prepared PVA/PEO/CHI nanofiber scaffolds via electrospinning technology. First, the hierarchical pore structure and elevated porosity stacked by nanofiber of the nanofiber scaffolds supplied suitable space for cell growth. Significantly, the PVA/PEO/CHI nanofiber scaffolds (the cytotoxicity of grade 0) effectively improved cell adhesion by regulating the CHI content, and presented positively correlated with the CHI content. Besides, the excellent surface wettability of PVA/PEO/CHI nanofiber scaffolds exhibited maximum absorbability at a CHI content of 15 wt%. Based on the FTIR, XRD, and mechanical test results, we studied the semi-quantitative effect of hydrogen content on the aggregated state structure and mechanical properties of the PVA/PEO/CHI nanofiber scaffolds. The breaking stress of the nanofiber scaffolds increased with increasing CHI content, and the maximum value reached 15.37 MPa, increased by 67.61 %. Therefore, such dual biofunctional nanofiber scaffolds with improved mechanical properties showed great potential application in tissue engineering scaffolds.

Sheath-core structured Ca-alginate/PVA aerogel fibers via directed freezing wet-spinning.

Biomass-based aerogel fibers have attracted increasing attention due to their renewable nature. However, their disadvantages, such as low mechanical strength, poor long-range order, and easy combustion, are still significant challenges. Herein, a directed freezing-assisted forced stretching strategy is developed to fabricate sheath-core structured Ca-alginate/polyvinyl alcohol (Ca-A/PVA) aerogel fibers with Long-range-ordered pores. The Ca-A/PVA aerogel fibers (3:2 m/m) exhibit the best comprehensive mechanical properties in terms of low thermal conductivity of 0.0524 W·m-1·K-1, a density of 0.1614 g·cm-3, a porosity of 89.9 %, a tensile strength of 8.72 MPa, a tensile modulus of 249.7 MPa, a toughness of 1.98 MJ∙m-3, and a self-extinguishing time from the fire of <1.2 s. The Ca-A/PVA fabrics showed a maximum absolute temperature difference of 11.4 °C at -20 °C and 14.0 °C at 60 °C compared to the plate temperature. The presented strategy is generalizable to other alginate-based aerogel fibers (e.g., alginate/guar gum).

Humidity-Responsive Guar Gum Fibers by Wet Spinning.

In this study, guar gum fibers were obtained by wet spinning, in which epichlorohydrin (ECH) and calcium chloride (CaCl2) were used as the cross-linking agent and metal complexing agent, respectively. The fibers' chemical structure, morphology, crystallinity, and thermal and mechanical properties were analyzed by Fourier infrared spectroscopy, scanning electron microscopy, and so forth. The results showed that ECH reacted with guar gum and formed ether bonds. Meanwhile, ECH can effectively increase the number of cross-linking points and improve the mechanical properties of the fibers. When the ECH content was 12% (w/w), the breaking strength could reach 2.4 cN/dtex. The conductivity of MC-GG fibers varied with the relative humidity and could reach 2.845 × 10-2 S/cm at maximum. Meanwhile, the contact angle of MC-GG fibers was 33°, indicating that the fibers had good hydrophilicity and humidity response ability and had excellent potential in the field of smart fabrics.

Characteristics of Sodium Alginate/Antarctic Krill Protein Composite Fiber Based on Cellulose Nanocrystals Modification: Rheology, Hydrogen Bond, Crystallization, Strength, and Water-Resistance.

The purpose of adding cellulose nanocrystals (CNCs) into sodium alginate (SA) and Antarctic krill protein (AKP) system is to use the ionic cross-linking of SA and AKP and the dynamic hydrogen-bonding between them and CNCs to construct multiple cross-linking structures, to improve the water-resistance and strength of SA/AKP/CNCs composite fiber. Based on the structural viscosity index in rheological theory, the ratio of spinning solution and temperature were optimized by studying the structural viscosity index of the solution under different CNCs content and temperature, then the composite fiber was prepared by wet spinning. We found that when the content of CNCs is 0.8% and 1.2%, the temperature is 45 °C and 55 °C, the structural viscosity is relatively low. Under the optimal conditions, the intermolecular hydrogen bonds decrease with the increase of temperature. Some of the reduced hydrogen bonds convert into intramolecular hydrogen bonds. Some of them exist as free hydroxyl; increasing CNCs content increases intermolecular hydrogen bonds. With the increase of temperature, the crystallinity of composite fiber increases. The maximum crystallinity reaches 27%; the CNCs content increases from 0.8% to 1.2%, the breaking strength of composite fiber increases by 31%. The water resistance of composite fiber improves obviously, while the swelling rate is only 14%.

Preparation and characterization of multi-network hydrogels based on sodium alginate/krill protein/polyacrylamide-Strength, shape memory, conductivity and biocompatibility.

Sodium alginate/krill protein/polyacrylamide (SA/AKP/PAM) hydrogel with "covalent bond-ion complex-hydrogen bond" multi-network structure was prepared by covalent cross-linking and complexion ion crosslinking using SA, AKP, and acrylamide (AM) as raw materials. The effects of ion species (Fe3+, Ba2+, Sr2+, Ca2+, and Zn2+) on the structure, morphology, and properties of multi-network hydrogels were studied in detail. The results showed that the mechanical strength of ionic cross-linked hydrogels increased significantly. The compressive strength of Fe3+ cross-linked hydrogels was 5.56 MPa, 16.13 times that of non-ionic crosslinked hydrogels. The results of ionic conductivity measurements showed that hydrogels had significant ionic conductivity and were sensitive to external forces. Interestingly, the hydrogel can be used as a capacitive pen in mobile phone writing, painting and dialing numbers. Moreover, ionic cross-linked hydrogels had a unique three-dimensional porous structure with gradient distribution, excellent shape memory effect, and good biocompatibility. Fe3+, Ba2+, Sr2+, and Ca2+ cross-linked hydrogels were nontoxic and conducive to the adhesion and growth of Schwann cells. These excellent properties of ionic cross-linked SA/AKP/PAM hydrogels have broad applications prospects in flexible electronic devices, sensors, soft electronic skins, and tissue engineering.

Preparation of Electrospun Polyvinyl Alcohol/Nanocellulose Composite Film and Evaluation of Its Biomedical Performance.

Using polyvinyl alcohol (PVA) and nanocellulose (NC) as raw materials, PVA/NC nanofiber membranes were prepared by electrospinning. The hydrogen bonding, crystalline properties and microscopic appearance of PVA/NC membranes with different NC contents were characterized. The mechanical properties, liquid absorption and cytotoxicity of the nanofiber membrane were evaluated. The results show that the free hydroxyl group of the PVA/NC nanofiber membranes have a maximum value of 9% at a mass fraction of 6% NC. The crystallinity of the PVA/NC nanofiber membranes and the average diameter of the nanofibers decreased and then increased as the NC content increased, with a minimum value of 38.23% and 272.03 nm, respectively, at 6% NC content. At this time, the contact angle was the smallest. The maximum strength of the PVA/NC nanofiber membranes is 75.8% higher than that of the PVA membrane at 2% NC content. With increasing NC content, the absorption of water, PBS sustained-release suspensions and artificial blood by PVA/NC nanofiber membranes increases. Cytotoxicity tests have shown that PVA/NC nanofiber membranes are non-toxic, have good cytocompatibility and are expected to be used in the field of medical dressings.

Hydrogen bonding in chitosan/Antarctic krill protein composite system: Study on construction and enhancement mechanism.

The main of the work concerns the reason for the interpretation of the tensile strength of chitosan (CS) enhanced by Antarctic krill protein (AKP). We found a new mixed solvent, 2 wt% glacial acetic acid, and 2 wt% ethylene glycol aqueous solution, to prepare a stable CS/AKP composite solution. Then we obtained CS/AKP fiber by wet-spinning on a lab-scale wet-spinning machine. The tensile strength of blended fibers is 2.53 cN/dtex in the dry state, which is improved by 11.9% compared with the CS fibers. We found that the increased tensile strength of the blended fibers is relative to the hydrogen bond formed between CS and AKP. Specifically, illustrate the restructured hydrogen bonds in CS/AKP system in Fourier transform infrared curve fitting. The hydrogen bond probably benefits on crystalline growth of CS along the fiber axis and is the main drivable factor in removing the water molecules in blended fibers.