Designing a superhydrophobic cotton fiber coating exploiting TiO2@g-C3N4 layered structure for augmented photocatalysis and efficient water-oil separation.

This study introduces a novel approach to develop a multifunctional coating on cotton fabric, emphasizing the utilization of cotton fiber as a biological macromolecule, by integrating a TiO2@g-C3N4 layered structure to confer superhydrophobic properties and multiple functionalities. The engineered structure not only enhances fabric roughness but also incorporates non-fluoro hydrophobic agents, thereby imparting diverse capabilities such as photocatalysis, oil-water separation, and self-cleaning to the cotton substrate. Fabrication of the TiO2@g-C3N4 layered structure involved ultrasonic dispersion of TiO2 and g-C3N4, subsequently deposited onto cotton fabric. Sequential hydrophobic treatment with polydimethylsiloxane (PDMS) and isophorone diisocyanate (IPDI) achieved superhydrophobicity, exhibiting an exceptional water contact angle (WCA) of 157.9°. Comprehensive characterization via scanning electron microscopy (SEM), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FT-IR), and thermogravimetric validated the composite's structural and chemical properties. The introduced TiO2@g-C3N4 structure significantly enhanced fabric roughness, while PDMS treatment lowered surface energy and IPDI hydrolysis facilitated cross-linking, ensuring durability. The resultant TiO2@g-C3N4/PDMS cotton exhibited outstanding self-cleaning properties and demonstrated oil adsorption capacity, accommodating both heavy and light oils. Notably, this superhydrophobic cotton efficiently separated water-oil mixtures, achieving 96.8 % efficiency even after 10 cycles. Moreover, under simulated light, it displayed outstanding photocatalytic degradation (93.2 %) of methylene blue while maintaining a WCA of 150° post-degradation, highlighting sustained functionality. This innovation holds promise for sustainable applications, offering robust physical and chemical durability within the realm of biological macromolecules. The amalgamation of TiO2@g-C3N4 layered structure and PDMS treatment on cotton fabric underscores a sustainable approach to address water-oil separation challenges and enable efficient self-cleaning. This research demonstrates a significant step towards sustainable material applications and addresses pertinent real-world challenges in diverse technological domains.

Artificial spinal dura mater made of gelatin microfibers and bioadhesive for preventing cerebrospinal fluid leakage.

Artificial spinal dura mater was designed by combining solution blow-spun gelatin microfibers and dopamine-capped polyurethane bioadhesive. Notably, the gelatin microfibers had a special pore structure, good water adsorption capability, and excellent burst pressure resistance. The bioadhesive layer contributed to the excellent sealing performance in the wet state. This material provides a promising alternative as an artificial spinal dura mater to prevent cerebrospinal fluid leakage.

Preparation of multifunctional cellulose macromolecule blended fabrics through internal and external synergy by N1, N6-bis (ethylene oxide-2-ylmethyl) hexane-1,6-diamine.

With the diversification of people's demand for textile functions, the preparation of multifunctional fabrics is still a current research hotspot. In this study, the water-soluble epoxy compound N1, N6-bis(oxiran-2-ylmethyl) hexane-1,6-diamine (EH) was introduced into cellulose macromolecule blended fabrics (cotton/modal) by two-phase vaporization technique, resulting in excellent wrinkle, hydrophobicity, and certain UV protection effects. It could be observed by electron microscopy that EH formed a polymer film on the fiber surface. In addition, the results of EDS scans and fiber swelling rate tests showed that EH was uniformly distributed and formed a cross-linked structure in the amorphous zones inside the fibers. Compared with the control fabrics, the wrinkle recovery angle of the EH-treated fabric was increased by 39.7 %. The fabrics could reach a contact angle of 136.9°, providing excellent hydrophobic effect. In addition, the fabrics achieved certain UV protection effects (UPF of 50+). The EH-treated fabrics were less stabilized in strong acid and alkali conditions, but exhibited greater durability in other environments. In summary, the internal and external synergistic effects of EH in forming polymer films on the fibers surface and internal cross-linking structures provided a cleaner, simple, and feasible method for the preparation of multifunctional cellulose macromolecule fibers textiles.

Anti-adhesive and antibacterial chitosan/PEO nanofiber dressings with high breathability for promoting wound healing.

Wound dressings are crucial for wound healing. Ideal wound dressings should possess many functions such as wettability, antibacterial activity and anti-adherent property to promote wound healing. In the present study solution blown spinning (SBS) technology was applied to prepare chitosan/polyethylene oxide (CS/PEO) nanofiber dressings in high efficiency. The obtained nanofiber dressings were treated with anhydrous ethanol to improve the fiber structure and enhance the functionality of the fiber dressings. The results show that the treated nanofibers had higher crystallinities and higher CS contents. The CS/PEO nanofiber dressings fabricated by using no additives and crosslinking had excellent wettability, water stability and antibacterial activity against Escherichia coli and Staphylococcus aureus reached to over 99.99 %. In addition, the CS/PEO nanofiber dressings exhibited high breathability, antioxidant activity and anti-adhesion function. The in vivo animal experiment confirmed that the nanofiber dressings enhanced cell proliferation and significantly accelerated the wound healing within 10 days. The developed CS/PEO nanofiber dressings have great potential in the clinical field of wound healing.

Hydroxyethyl methyl cellulose controls the diffusion behavior of pico-liter scale ink droplets on silk to improve inkjet printing performance.

In this study, a simple and effective coating method to improve printing quality and material utilization rate was proposed. The flow behavior of pico-liter scale ink droplets on the silk fabric surfaces which treated separately with Sodium alginate (SA), Hydroxyethyl cellulose (HEC) and Hydroxyethyl methyl cellulose (HEMC) was observed and measured. Indeed, based on the direct empirical results, the optimal pretreatment process on the fabrics, aiming to increase the ink utilization rate and further improve the surface printing clarity, has been obtained in the experiments. Studies on rheological property, surface activity, scanning electron microscope (SEM) and contact angle have shown that HEMC can form the densest and smoothest film on silk fabrics, where the most hydrophobic surface arises. X-ray photoelectron spectroscopy (XPS) results indicate that the surface of the fabric is covered with films of different properties formed by the treatment solution, and confirmed that the films formed by HEMC were more hydrophobic. The spreading motion of ink droplets revealed that although the hydrophobicity of HEC and HEMC effectively restrain the flow of ink droplet along the fiber, and the length and width of one-ink droplet deposition are minimum in HEMC treated fabric. Similarly, the findings on color performance suggest that HEMC has absolutely comparative advantage over HEC in improving the color effect of printing, with dye utilization rate of three different colors increasing by 68.7 %-80.0 %.

Potential use of bioactive nanofibrous dural substitutes with controlled release of IGF-1 for neuroprotection after traumatic brain injury.

For patients suffering from traumatic brain injury (TBI), the closure of dural defects after decompressive craniectomy is the prerequisite to restoring normal physiological functions. It is also an urgent challenge to provide a neuroprotection effect against the primary and secondary nerve damage during long-term recovery. To solve these issues, we herein develop a class of bioactive, nanofibrous dural substitutes that can long-term release insulin-like growth factor 1 (IGF-1) for improving the survival and neurite outgrowth of neural cells after TBI. Such dural substitutes were polycaprolactone (PCL) nanofibers encapsulated with hyaluronic acid methacryloyl (HAMA)/IGF-1 by blend or coaxial electrospinning techniques, achieving bioactive PCL/HAMA/IGF nanofibrous dural substitutes with different release profiles of IGF-1. The nanofibrous dural substitutes exhibited good mechanical properties and hydrophobicity, which prevent cerebrospinal fluid leakage, maintain normal intracranial pressure, and avoid external impact on the brain. We also found that the viability and neurite outgrowth of SH-SY5Y cells and primary neurons were significantly enhanced after neurite transection or oxygen and glucose deprivation treatment. Taken together, such PCL/HAMA/IGF nanofibrous dural substitutes hold promising potential to provide neuroprotection effects after primary and secondary nerve damage in TBI, which would bring significant benefits to the field of neurosurgery involving the use of artificial dura mater.

In Situ Generated UiO-66/Cotton Fabric Easily Recyclable for Reactive Dye Adsorption.

In view of the environmental pollution caused by the widespread use of reactive dyes in the printing and dyeing industry, the modified cotton fabric was loaded with the extremely stable metal-organic frame (MOF) material UiO-66 for removing reactive dyes from colored wastewater. UiO-66/cotton fabric was prepared by in situ synthesis, and its surface morphology and structure were analyzed by XRD, SEM, BET, and XPS. The adsorption performance of UiO-66/cotton fabric on reactive dyes was investigated by adsorbent dosage, adsorption time and temperature, dye concentration, pH, and so on. The results indicated that the adsorption equilibrium time of UiO-66/cotton fabric on reactive orange 16 was 120 min, and the removal rate was about 98%. The adsorption process belongs to simple molecular layer chemisorption and can be regarded as a spontaneous heat absorption reaction, which was consistent with the proposed secondary kinetic model and Langmuir isothermal adsorption model. In addition, the reactive dyes with a higher molecular weight of each sulfonic acid group are more hydrophobic, and the dyes are more likely to aggregate and deposit on the adsorbent surface by electrostatic attraction, hydrogen bonding, and π-π accumulation. Therefore, this work provides a potential UiO-66/cotton fabric application for the effective adsorption of reactive dyes in textile wastewater.

Preparation of zeolitic imidazolate framework-67/wool fabric and its adsorption capacity for reactive dyes.

Zeolitic imidazolate framework-67 (ZIF-67) formed by Co2+ and 2-methylimidazole (MIM) is widely used for adsorption and separation of pollutants. However, there are some disadvantages for ZIF-67 powder, such as strong electrostatic interaction and difficulty in recovery from the liquid phase. The available way to solve the above problems is choosing a suitable substrate to load ZIF-67. The amino and hydroxyl of wool fabrics effectively capture and fix ZIF-67, making it easy to separate ZIF-67 by taking out the composite materials from aqueous solution. In this study, ZIF-67/Wool fabric (ZW) was successfully prepared. The results show that ZIF-67 has better adsorption performance for reactive dyes with more sulfonic groups, higher molecular weight and lower steric resistance. The equilibrium adsorption capacity of ZW for reactive red 195 was 4.15 mg g-1. The adsorption accorded with pseudo-second-order kinetic model and Langmuir isotherm. This study improved the application of ZIF-67, which provided a treatment method for dyeing wastewater and made it possible to recycle waste wool.

Fabrication of Chitosan-Loaded Multifunctional Wool Fabric for Reactive Dye Digital Inkjet Printing by Schiff Base Reaction.

Improving the development of high-value multifunctional wool fabrics was essential to satisfy diverse needs. Considering the various characteristics of chitosan macromolecules, herein, a padding-cross-linking process was adopted and then multifunctional wool fabrics with outstanding printing effects, shrink resistance, and antibacterial properties were fabricated. The test results showed that chitosan macromolecules loaded successfully on the wool fiber surface by Schiff base reaction. Wool fabrics changed from hydrophobic to hydrophilic due to the existence of chitosan macromolecules. The color strength (K/S value) of the reactive dye inkjet-printed wool fabric was greatly increased from 20.48 to 26.6. The area shrinkage of final samples was 2.53%, which was exceedingly lower than that of the original wool (10.96%). Moreover, the chitosan macromolecules with reactive amino groups endowed wool fabrics with certain antibacterial properties against E. coli and S. aureus. Generally, this study provided guidance for manufacturing multifunctional digital inkjet-printed wool products in mass production.

Nanocellulose with unique character converted directly from plants without intensive mechanical disintegration.

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).

A Water-Soluble Epoxy-Based Green Crosslinking System for Stabilizing PVA Nanofibers.

With the ever-growing concern about environmental conservation, green production and water-based nanofibers have attracted more and more interest from both academic and industrial fields; nevertheless, the stabilization process of water-based nanofibers is primarily relying on the application of organic solvent-based crosslinking agents. In this work, we develop a green approach to fabricate water-resistant polyvinyl alcohol (PVA) nanofibers by using a water-based epoxy compound, N1, N6-bis(oxiran-2-ylmethyl) hexane-1,6-diamine (EH), as the crosslinker. This EH/sodium carbonate/sodium bicarbonate (CBS) solution system can break down large aggregates of PVA molecules into small ones and promote the uniform distribution of EH in the solution, resulting in the improved stability of crosslinked PVA nanofibers. We firstly report that the uniform dispersion of crosslinking agents in the electrospinning solution plays a vital role in improving the stability of spinning solutions and the water resistance of crosslinked PVA nanofibers by comparing crosslinking performances between water-based epoxy and conventional water-based blocked isocyanate (BI). This work could open up a novel strategy and green approach for the stabilization of water-based nanofibers.

Flower-Shaped Ni/Co MOF with the Highest Adsorption Capacity for Reactive Dyes.

Reactive dyes are widely used in textile industry, but their excessive use has caused several water pollution problems. In order to reasonably treat printing and dyeing wastewater, the highly efficient adsorbent for reactive dyes employed in this study is a new type metal-organic framework (MOF) material. Ni/Co MOF (NCM) was synthesized using the solvothermal method; then, the materials were analyzed by a series of characterization methods. This study mainly investigated the adsorption properties of NCM toward reactive dyes, and the adsorption capacities of NCM toward reactive red 218 were up to 200 mg·g-1. The results were found to conform to the Langmuir isotherm model, and the pseudo-second-order kinetic model by performing kinetic and isotherm studies on the adsorption process of reactive red 218 on NCM. The results of the intraparticle diffusion model suggest that the binding of reactive red 218 to NCM was mainly divided into three steps: adsorption, diffusion, and saturation. Moreover, it was concluded by thermodynamic fitting of the adsorption process that the adsorption of reactive red 218 by NCM proceeded spontaneously and was accompanied by an endothermic reaction, in which the adsorption of both occurred mainly by electrostatic attraction. The NCM has good reusability and still has good adsorption performance after being reused 5 times. Therefore, NCM is a very promising and excellent adsorbent for the treatment of dye wastewater because of its high efficiency and reusability.

Scalable Nano Building Blocks of Waterborne Polyurethane and Nanocellulose for Tough and Strong Bioinspired Nanocomposites by a Self-Healing and Shape-Retaining Strategy.

Nature has given us significant inspiration to reproduce bioinspired materials with high strength and toughness. The fabrication of well-defined three-dimensional (3D) hierarchically structured nanocomposite materials from nano- to the macroscale using simple, green, and scalable methods is still a big challenge. Here, we report a successful attempt at the fabrication of multidimensional bioinspired nanocomposites (fiber, films, plates, hollow tubes, chair models, etc.) with high strength and toughness through self-healing and shape-retaining methods using waterborne polyurethane (WPU) and nanocellulose. In our method, the prepared TEMPO oxide cellulose nanofiber (TOCNF)-WPU hybrid films show excellent moisture-induced self-healing and shape-retaining abilities, which can be used to fabricate all sorts of 3D bioinspired nanocomposites with internal aligned and hierarchical architectures just using water as media. The tensile and flexural strength of the self-assembled plate can reach 186.8 and 193.2 MPa, respectively, and it also has a high toughness of 11.6 MJ m-3. Because of this bottom-up self-assembly strategy, every multidimensional structure we processed has high strength and toughness. This achievement would provide a promising future to realize a large-scale and reliable production of various sorts of bioinspired multidimensional materials with high strength and toughness in a sustainable manner.

Insights into coloration enhancement of mercerized cotton fabric on reactive dye digital inkjet printing.

Mercerization can improve the utilization rate of dyes in the dyeing process, and reduce the discharge of washing wastewater. However, the effect and mechanism of mercerization is not clear on digital inkjet printing of cotton fabric. In this work, two kinds of cotton fabrics (original and mercerized) were used for reactive dye digital inkjet printing, and the color improvement mechanism of caustic soda mercerization was investigated. It was found that the crystallinity of cotton fibre was adjusted from 73.9% to 58.5% by caustic mercerization, and the breaking strength did not decrease compared with original cotton fibre. Thus, the accessible reactive hydroxyl groups and the wettability were enhanced for treated cotton fibres, which promoted the inks' wick into the fibres. Interestingly, the penetration of ink droplets between the yarns and fibres after caustic mercerization was decreased, thus the dyes mainly gathered on the surface of cotton fabric. The cotton fibres' cross section structure changed from flat oval to round, which increased the contact area between reactive dyes and fibres. At a certain amount of ink, the optimal K/S value of 23.47 was achieved for treated cotton fabrics, which was higher than that of untreated cotton fabrics (17.15). Meanwhile, the printed fabrics displayed good washing fastness, rubbing fastness and glossiness. This work has important theoretical guiding significance for producing high quality mercerized cotton fabric digital printing products and reducing printing wastewater discharge.

Improving Biocompatibility of Polyester Fabrics through Polyurethane/Gelatin Complex Coating for Potential Vascular Application.

Medical apparatus and instruments, such as vascular grafts, are first exposed to blood when they are implanted. Therefore, blood compatibility is considered to be the critical issue when constructing a vascular graft. In this regard, the coating method is verified to be an effective and simple approach to improve the blood compatibility as well as prevent the grafts from blood leakage. In this study, polyester fabric is chosen as the substrate to provide excellent mechanical properties while a coating layer of polyurethane is introduced to prevent the blood leakage. Furthermore, gelatin is coated on the substrate to mimic the native extracellular matrix together with the improvement of biocompatibility. XPS and FTIR analysis are performed for elemental and group analysis to determine the successful coating of polyurethane and gelatin on the polyester fabrics. In terms of blood compatibility, hemolysis and platelet adhesion are measured to investigate the anticoagulation performance. In vitro cell experiments also indicate that endothelial cells show good proliferation and morphology on the polyester fabric modified with such coating layers. Taken together, such polyester fabric coated with polyurethane and gelatin layers would have a promising potential in constructing vascular grafts with expected blood compatibility and biocompatibility without destroying the basic mechanical requirements for vascular applications.

Organometallic Magnesium Complex with Aggregation Induced Emission Properties: Synthesis, Characterization, and Fluorescent Fibers Applications.

In this work, a novel organomagnesium complex with outstanding aggregation induced emission (AIE) properties is synthesized using dibenzoylmethane (DBM) as the ligand. The structure of the complex is confirmed to be one magnesium ion coordinated to the dione groups of two DBM molecules, and the magnesium ion adopts a distorted octahedrally geometry. The obvious emission is found for Mg(DBM)2 powder and not in the solution, making this the first reported organomagnesium complex with AIE property. The properties of the complex were investigated by using UV-vis absorption and fluorescence emission spectroscopy, cyclic voltammetry, and density functional theory calculations. Moreover, the Mg(DBM)2 solution dispersed in filter paper was is colorless, which may be made into a convenient anti-counterfeiting and encryption tool. Mg(DBM)2 /alginate fibers were prepared by wet-spinning process and further processed into paper, which can be used in the fields of sensors, anti-counterfeiting, and encryption. Sweat contains a wealth of chemical information that could potentially indicate the body's deeper biomolecular state. The prepared fluorescent fibers were used to detect sweat due to its non-toxic, low-cost efficient and fast response to analytes.

Hierarchical Bi2MoO6 microsphere photocatalysts modified with polypyrrole conjugated polymer for efficient decontamination of organic pollutants.

To effectively degrade organic pollutants in wastewater, visible-light-driven Bi2MoO6/PPy hierarchical heterogeneous photocatalysts were prepared through a solvothermal method and the following in-situ chemical oxidation polymerization. Compared with pristine Bi2MoO6 photocatalyst, the composite photocatalysts exhibited dramatically improved photocatalytic activity and photostability towards the degradation of methylene blue dye and tetracycline antibiotic. Bi2MoO6/PPy-80 sample achieved the highest photocatalytic degradation rates for methylene blue dye (93.6%) and tetracycline antibiotic (88.3%) under visible light irradiation. These two organic pollutants could be completely degraded into nontoxic small molecules according to in-depth HPLC-MS analysis of degradation products. The transient photocurrent responses, electrochemical impedance spectra, and photoluminescence spectra demonstrated that the introduction of PPy nanoparticles on the surface of Bi2MoO6 nanosheets could effectively accelerate the separation of photo-generated electron-hole pairs. Furthermore, a possible synergetic photocatalytic mechanism was put forward based on the electron spin resonance and XPS valence-band spectra. This work indicated that construction of hierarchical composite photocatalysts combining polypyrrole conductive polymer and Bi2MoO6 semiconductor in nanoscale is an efficient approach to improve photocatalytic activity for environmental remediation.

Controlling the Spreading of Nanoliter-Scale Droplets on the Fibers of Fabrics for Enhancing Image Quality and Ink Utilization.

Electronic and traditional textiles have been widely manufactured through inkjet printing. However, nanoliter-scale ink droplets tend to excessively spread along the fiber direction, which results in poor image quality and low ink utilization. Here, hydroxyethyl cellulose (HEC) and hydroxypropyl methyl cellulose (HPMC) were introduced to control the spreading of nanoliter-scale droplets on cotton fabrics. The results showed that both HEC and HPMC could reduce the spreading of nanoliter droplets along the fibers through increasing the hydrophobicity of the fabric. However, the effect of HPMC was much better than that of HEC due to its higher surface activity. The flow of nanoliter droplets along the fibers was well consistent with the Washburn function. After HPMC treatment, the depositing length of one droplet reduced from beyond 200 µm to about 50 µm. The imaging quality was greatly improved. In addition, the dye utilization increased by 33-78% due to the decrease in the diffusion of dye solution to the back of the fabric. This study is of great significance for improving the quality of inkjet printing and the utilization of depositing materials, particularly expensive materials.

Strategy to Fabricate a Strong and Supertough Bio-Inspired Fiber with Organic-Inorganic Networks in a Green and Scalable Way.

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.

Effect of Diethylene Glycol on the Inkjet Printability of Reactive Dye Solution for Cotton Fabrics.

Digital inkjet printing technology plays an increasingly important role in textile printing. The printing printability of reactive dye inks is the key to improving the quality of printed fabrics. In this study, an eco-friendly and simple method to improve the inkjet printability of reactive dye solutions was proposed. The influence of diethylene glycol on the surface tension, rheology, and dye molecule aggregation properties for three reactive dye solutions was investigated. The jetting performance of dye solutions was explored by observing droplet formation. Moreover, the color performance of printed cotton fabrics, including reactive dye solution penetration, colorimetric values, and color strength, was evaluated. Addition of diethylene glycol could change the aggregation of dye molecules by hydrophobic forces and hydrogen bonds. Diethylene glycol could inhibit formation of satellite droplets by changing the viscosity and surface tension of solutions, which made the pattern printed on cotton fabrics show regular edge sharpness. Furthermore, the dye solutions containing 10% DEG not only satisfied various properties of reactive dye inks but also had the highest color strength and the deepest and brightest colors.