Durable, multifunctional cotton fabrics with in situ deposited micro/nanomaterials for effective self-cleaning, oil-water separation and antibacterial activity.

The facile modification of cotton fabrics for excellent self-cleaning, oil-water separation, and antibacterial activity is of great interest for multifunctional requirements. Herein, a durable, robust, fluorine-free multifunctional cotton fabric was fabricated via in-situ growing zeolitic imidazolate framework-67 (ZIF-67) on the cotton surface, followed by depositing hydrophobic SiO2 (H-SiO2) nanoparticles synthesized via an improved Stöber reaction. Meanwhile, the abundant hydroxyls of the cotton fabrics provided the necessary ion interaction sites for the uniform deposition of micro/nanomaterials, confirmed by the visualized Raman imaging technology. The resultant H-SiO2/ZIF-67@cotton fabric exhibited superhydrophobicity with a water contact angle of 159° and versatile self-cleaning, antifouling, oil-water separation, as well as prominent antibacterial activity against S. aureus and E. coli. At the same time, the superhydrophobic cotton fabric possessed excellent durability and stability against harsh environments, including abrasion, washing, acid, base, salt, and organic solvents. This facile technique can be applied for large-scale production of multifunctional superhydrophobic cotton fabrics due to its easy operation, low cost, and environmental friendliness.

Aesthetic Cellulose Filaments with Water-Triggered Switchable Internal Stress and Customizable Polarized Iridescence Toward Green Fashion Innovation.

Healthy, convenient, and aesthetic hair dyeing and styling are essential to fashion trends and personal-social interactions. Herein, we fabricate green, scalable, and aesthetic regenerated cellulose filaments (ACFs) with customizable iridescent colors, outstanding mechanical properties, and water-triggered moldability for convenient and fashionable artificial hairdressing. The fabrication of ACFs involves cellulose dissolution, cross-linking, wet-spinning, and nanostructured orientation. Notably, the cross-linking strategy endows the ACFs with significantly weakened internal stress, confirmed by monitoring the offset of the C-O-C group in the cellulose molecular chain with Raman imaging, which ensures a tailorable orientation of the nanostructure during wet stretching and tunable iridescent polarization colors. Interestingly, ACFs can be tailored for three-dimensional shaping through a facile water-triggered adjustable internal stress: temporary shaping with low-level internal stress in the wet state and permanent shaping with high-level internal stress in the dry state. The health, convenience, and green aesthetic filaments show great potential in personal wearables.

Nitrogen-Doped Carbon Networks with Consecutive Conductive Pathways from a Facile Competitive Carbonization-Etching Strategy for High-Performance Energy Storage.

Recently, new carbonization strategies for synthesizing structure-controlled and high-performance carbon electrode materials have attracted great attentions in the field of energy storage and conversion. Here a competitive carbonization-etching strategy to prepare nitrogen-doped carbon polyhedron@carbon nanosheet (NCP@CNS) hybrids derived from zeolitic imidazolate framework-8 is presented. Consecutive conductive networks are constructed in the NCP@CNS hybrids during a unique carbonization-etching pyrolysis, where a competition between the formation of NCPs and CNSs exists. When the NCP@CNS hybrids are employed as supercapacitor electrodes, their hierarchically porous NCPs serve as ion-buffering reservoirs for offering fast ion transport channels, and the CNSs within hybrids not only link the NCPs together to build electron transfer pathways but also restrict the volume fluctuation of electrodes during charging and discharging process. As a result, the as-fabricated NCP@CNS electrode displays excellent electrochemical performances including a superior specific capacitance of 320 F g-1 , a high energy density of 22.2 W h kg-1 (5.6 W h kg-1 for symmetric device), and a long cycle life with capacitance retention of ≈101.8% after 5000 cycles. This study opens an encouraging avenue toward the tailored synthesis of metal-organic frameworks (MOFs)-derived carbon electrodes for renewable energy storage applications and devices.

Sustainable Fenton-like degradation of methylene blue over MnO2-loaded poly(amidoxime-hydroxamic acid) cellulose microrods.

Catalysts based on cellulose/metal oxide hybrids are considered effective for the remediation of dye wastewater. However, the difficult recovery of commonly used nanocellulose and the weak binding strength of metal oxide nanoparticles restrict their wide application. Herein, MnO2 nanoparticle-loaded poly(amidoxime-hydroxamic acid) modified microcrystalline cellulose (pAHA-MCC@MnO2) catalysts were synthesized via an oximation reaction followed by in-situ growth. Morphology, crystallinity and textural characteristics of pAHA-MCC before and after deposition of MnO2 nanoparticles were characterized by SEM, EDS, FTIR, XRD and XPS analyses. The main results indicated the formation of hierarchical porous structured cellulose microrods with uniform distribution of hydrangea flower-like MnO2 nanoparticles. In the presence of H2O2, pAHA-MCC@MnO2 displayed good catalytic performance toward the degradation of methylene blue (MB) over a wide pH range of 3-10, due to the advanced Fenton-like catalysis. Reaction conditions, such as amount of H2O2 used, the initial MB concentration and catalyst dosage were also investigated. The optimized system showed 97.6% removal of MB in 25 min for 100 mg/L MB solution, with very little decrease in performance after 5 cycles. This work provides a facile and promising strategy for the development of biodegradable and sustainable architectures capable of efficiently degrading dye wastewater.

Efficient Congo Red Removal Using Porous Cellulose/Gelatin/Sepiolite Gel Beads: Assembly, Characterization, and Adsorption Mechanism.

Porous sustainable cellulose/gelatin/sepiolite gel beads were fabricated via an efficient 'hydrophilic assembly-floating droplet' two-step method to remove Congo red (CR) from wastewater. The beads comprised microcrystalline cellulose and gelatin, forming a dual network framework, and sepiolite, which acted as a functional component to reinforce the network. The as-prepared gel beads were characterized using FTIR, SEM, XRD, and TGA, with the results indicating a highly porous structure that was also thermally stable. A batch adsorption experiment for CR was performed and evaluated as a function of pH, sepiolite addition, contact time, temperature, and initial concentration. The kinetics and isotherm data obtained were in agreement with the pseudo-second-order kinetic model and the Langmuir isotherm, with a maximum monolayer capacity of 279.3 mg·g-1 for CR at 303 K. Moreover, thermodynamic analysis demonstrated the spontaneous and endothermic nature of the dye uptake. Importantly, even when subjected to five regeneration cycles, the gel beads retained 87% of their original adsorption value, suggesting their suitability as an efficient and reusable material for dye wastewater treatments.

Synthesis of TiO2NWS@AuNPS Composite Catalyst for Methylene Blue Removal.

In this article, HBP-NH2-modified titania nanowire (TiO2NWS)-decorated Au nanoparticles (TiO2NWS@AuNPS) were synthesized by one-step method. The role of HBP-NH2 concentration in the formation of TiO2NWS was investigated. The fineness and uniformity of pure TiO2NWS were enhanced by absorbed amino groups from amino-terminated hyperbranched polymer (HBP-NH2). The morphology and crystal structure of TiO2NWS and TiO2NWS@AuNPS were examined by transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fournier transform infrared (FTIR) spectroscopy. The chemical states of gold, titanium and oxygen were analyzed by X-ray photoelectron spectroscopy (XPS). The results showed that at the concentration of HBP-NH2 100 g/L, the mean diameter of TiO2NWS was nearly 72 nm and Au nanoparticles were uniformly distributed on the surface of TiO2NWS. The presence of AuNPS improved the photocatalytic properties of TiO2NWS under UV light irradiation. The Au load was believed to improve the utilization rate of the photoelectron and activated the adsorbed oxygen. The obtained TiO2NWS@AuNPS decomposed 99.6% methylene blue (MB) after 300 min when subjected to UV light irradiation. After five cycles of the catalyzing process, the TiO2NWS@AuNPS still retained over 90% of its catalytic ability for MB. The Au deposition was found responsible for the high catalytic activity of TiO2NWS@AuNPS.

Cellulose/polymer/silica composite cotton fiber based on a hyperbranch-mesostructure system as versatile adsorbent for water treatment.

The present study describes the preparation of a hybrid cellulose-based adsorbent (HM-cotton) containing a dot-plane composite adsorption system. The dot-plane adsorption structure is formed by the plane of hyperbranched polymer (HBP) layer distributed by the functional mesoporous nanoparticle (CA-MSN) dots, fabricating hyperbranch-mesostructure system via self-assembly. The resultant adsorbent HM-cotton was characterized, and the adsorption mechanism for dyes and metal ions was also discussed in detail. The results show that the adsorption data is fitted to Pseudo-second-order kinetic model and Langmuir isotherm model, and owing to the dot-plane system possessing functional mesostructure of CA-MSNs with large surface area and substantial adsorption sites from HBP macromolecules, HM-cotton exhibits versatile, highly-efficiency and sustainable adsorption properties for dyes such as CR and MB, and metal ions such as Fe3+ and Cu2+ from aqueous media. The saturated adsorption capacities are 243.7, 165.4, 143.8 and 119.1mg/g for CR, MB, Fe3+ and Cu2+, respectively.

Sodium alginate/graphene oxide aerogel with enhanced strength-toughness and its heavy metal adsorption study.

Ordered porous sodium alginate/graphene oxide (SAGO) aerogel was fabricated by in situ crosslinking and freeze-drying method. GO, as reinforcing filler, can be easily incorporated with SA matrix by self-assembly via hydrogen bonding interaction. Compared with pure SA aerogel, the as-prepared SAGO exhibited excellent mechanical strength and elasticity, and the compression strength of SAGO can reach up to 324 kPa and remain 249 kPa after five compression cycles when 4 wt% GO was added, which were considered significant improvements. SEM result presents that the addition of GO obviously improves the porous structures of aerogel, which is beneficial for the enhancement of strength-toughness and adsorbability. As a consequence, the adsorption process of SAGO is better described by pseudo-second-order kinetic model and Langmuir isotherm, with maximum monolayer adsorption capacities of 98.0 mg/g for Cu2+ and 267.4 mg/g for Pb2+, which are extremely high adsorption capacities for metal ions and show far more promise for application in sewage treatment.