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Adsorptive membranes for the efficient separation of dyes with the same charges are quite desirable. Herein, a novel membrane of lanthanum hydroxide/cellulose hydrogel coated filter paper (LC) was prepared through a facile strategy of dip-coating followed by freeze-shaping. With the aid of cellulose gel, the generated La(OH)3 achieved fine dispersion. In addition, the pore size of LC membrane could be regulated by altering the cellulose concentration or the lanthanum chloride dosage, which was crucial for its water flux. In particular, the obtained membrane possessed a high water flux (128.4 L m-2 h-1) and a high dye rejection (97.2 %) for anionic Congo red (CR) only driven by the gravity, which outperformed many previously reported membranes. More intriguingly, its dye rejection for anionic methyl orange (MO) was only 0.9 %, exhibiting high selectivity for dyes with the same charges. Single-solute adsorption experiments indicated that the CR adsorption on the membrane was best fitted by the pseudo-first-order kinetic model, and it followed the Langmuir monolayer adsorption mechanism.

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In this work, a unique three-dimensional nanofibrous foam of cellulose@g-C3N4@Cu2O was prepared via electrospinning followed by a foaming process. A cellulose solution in DMAc/LiCl containing g-C3N4 and CuSO4 was applied for electrospinning, while aqueous alkali was used as the coagulation bath. The solidification of electrospun cellulose/g-C3N4 nanofibers would be accompanied with in-situ formation of Cu(OH)2 nanoparticles. Interestingly, the hydrogen gas (H2) generated from NaBH4 could transform the two-dimensional membrane into a three-dimensional foam, leading to the increased specific surface area and porosity of the material. Meanwhile, the Cu(OH)2 nanoparticles attached on the electrospun nanofibers were reduced to Cu2O to form a p-n heterostructure between Cu2O and g-C3N4. The as-prepared cellulose@g-C3N4@Cu2O foam exhibited a high degradation efficiency (99.5 %) for the dye of Congo Red under visible light radiation. And ·O2- was discovered to be the dominant reactive species responsive for dye degradation. Moreover, the cellulose@g-C3N4@Cu2O could maintain its initial degradation efficiency even after seven cycles of reuse, suggesting the excellent stability and cycling performance.

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Despite of the fact that polymers have brought tremendous convenience to human life, they have also inevitably caused considerable environmental pollution after their service life. Therefore, a feasible strategy that can effectively recycle waste polymers and endow them with high added value is much desired. Superwetting materials have shown great promise in oily wastewater treatment because of their high oil/water separation efficiency. However, most of these materials present some limitations, such as complex preparation procedures and poor salt tolerance, which hamper their practical applications. In this study, an iron hydroxide@polydopamine@waste polyurethane foam (Fe(OH)3@PDA@WPU) was synthesized via a facile and mild "one-pot" reaction. During this process, polymerization of dopamine and in situ growth of Fe(OH)3 were simultaneously realized, and the resultant PDA and Fe(OH)3 nanoparticles were firmly attached to the surface of WPU. Due to the abundant hydrophilic groups from PDA and Fe(OH)3 coupled with the surface roughness created by Fe(OH)3 nanoparticles, the surface properties of the foam could be changed from hydrophobic to superhydrophilic. Remarkably, the Fe(OH)3@PDA@WPU was capable of separating various oil/water mixtures even under some severe conditions (e.g. erosion in a saturated sodium chloride solution and longtime sonication), demonstrating high potential in marine oily sewage treatment. Moreover, this work also paved a new path for reducing the negative impact of waste polymer foams on our environment, and in the meantime realizing their high value utilization.

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Electrospun cellulose nanofiber nonwovens have shown promise in wound dressing owing to the highly interconnected pore structure, high hydrophilicity coupled with other coveted characteristics of biodegradability, biocompatibility and renewability. However, electrospun cellulose wound dressings with loaded drugs for better wound healing have been rarely reported. In this study, a novel wound dressing with a high drug loading capacity and sustained drug release properties was successfully fabricated via electropinning of cellulose followed by polyethylenimine (PEI)-functionalization. Remarkably, the grafted PEI chains on the surface of electrospun cellulose nanofibers provided numerous active amino groups, while the highly porous structure of nonwovens could be well retained after modification, which resulted in enhanced adsorption performance against the anionic drug of sodium salicylate (NaSA). More specifically, when immersed in 100 mg/L NaSA solution for 24 h, the as-prepared cellulose-PEI nonwoven displayed a multilayer adsorption behavior. And at the optimal pH of 3, a high drug loading capacity of 78 mg/g could be achieved, which was 20 times higher than that of pristine electrospun cellulose nonwoven. Furthermore, it was discovered that the NaSA-loaded cellulose-PEI could continuously release the drug for 12 h in simulated body fluid (SBF), indicating the versatility of cellulose-PEI as an advanced wound dressing with drug carrier functionalities.

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A unique iron/carbon aerogel (Fe/CA) was prepared via pyrolysis using ferric nitrate and bamboo cellulose fibers as the precursors, which could be used for high-efficiency removal of toxic Cr(VI) from wastewaters. Its composition and crystalline structures were characterized by FTIR, XPS, and XRD. In SEM images, the aerogel was highly porous with abundant interconnected pores, and its carbon-fiber skeleton was evenly covered by iron particles. Such structures greatly promoted both adsorption and redox reaction of Cr(VI) and endowed Fe/CA with a superb adsorption capacity of Cr(VI) (182 mg/g) with a fast adsorption rate (only 8 min to reach adsorption equilibrium), which outperformed many other adsorbents. Furthermore, the adsorption kinetics and isotherms were also investigated. The experiment data could be much better fitted by the pseudo-second-order kinetics model with a high correlating coefficient, suggesting that the Cr(VI) adsorption of Fe/CA was a chemical adsorption process. Meanwhile, the Langmuir model was found to better describe the isotherm curves, which implied the possible monolayer adsorption mechanism. It is noteworthy that the aerogel adsorbent as a bulk material could be easily separated from the water after adsorption, showing high potential in real-world water treatment.

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Carbon aerogels (CA) derived from bamboo cellulose fibers were coupled with TiO2 to form CA/TiO2 hybrids, which exhibited extraordinary performance on the photo-catalytic degradation of methylene blue (MB). The structure and morphology of CA/TiO2 were characterized by field emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and Raman spectrum. The CA displayed a highly porous and interconnected three-dimensional framework structure, while introducing the catalytic active sites of TiO2 onto the aerogel scaffold could remarkably enhance its photo-catalytic activity. The adsorption and photo-catalytic degradation of MB by the CA/TiO2 hybrid were investigated. The maximum adsorption capacity of CA/TiO2 for MB was 18.5 mg/g, which outperformed many similar materials reported in the literature. In addition, compared with other photo-catalysts, the present CA/TiO2 demonstrated superior photo-catalytic performance. Almost 85% of MB in 50 mL solution with a MB concentration of 10 mg/L could be effectively degraded by 15 mg CA/TiO2 in 300 min.

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While of enormous scientific interests, the super-wetting materials capable of one-step separation of oils and dyes from water are rare on the market. Besides, the disposal of the used materials themselves is still a challenge, mainly ascribed to their non-biodegradation. Herein, we report an all-cellulose composite membrane that can simultaneously remove oil and dye from water. The membrane was fabricated via a simple dip-coating process during which the filter paper was coated by a cellulose hydrogel layer. This cellulose hydrogel coating was discovered to play an essential role in the separation of oil/water emulsion. Meanwhile, the incorporation of citric acid remarkably improved the mechanical and adsorption properties of the membrane as it served as both the crosslinking agent and the active species for methylene blue adsorption. This work demonstrated a new strategy on the development of fully biodegradable materials for both high-efficiency oil/water separation and dye removal.

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Nanocellulose-derived carbon is a promising material in energy storage because of its sustainability, low environmental impact, and large specific surface area. Herein, the skin secretion of Andrias davidianus (SSAD) is applied for the first time as the bio-nitrogen source to dope carbon aerogels from nanocellulose. Cellulose nanocrystal (CNC) is discovered to be very effective to address the dispersion problem of SSAD in water. After being homogeneously mixed with cellulose nanofiber (CNF), honeycomb-structured nanofibrous carbon aerogels are obtained via unidirectional freeze-drying of the SSAD/CNC/CNF mixture followed by high-temperature carbonization. Impressively, unlike those fragile carbon aerogels in many early works, the present ones exhibit outstanding elasticity in repeated compression and release tests. Moreover, a symmetric binder-free supercapacitor is assembled from the carbon aerogels, which exhibits improved electrochemical capacitive properties and cycling stability. And even after 500 compression and release cycles, the supercapacitor can still maintain high capacitive performance, indicating its superiorities in durability and electrochemical stability.

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Inspired from fishscales, membranes with special surface wettability have been applied widely for the treatment of oily waste water. Herein, a novel superhydrophilic graphene oxide (GO)@electrospun cellulose nanofiber (CNF) membrane was successfully fabricated. This membrane exhibited a high separation efficiency, excellent antifouling properties, as well as a high flux for the gravity-driven oil/water separation. Moreover, the GO@CNF membrane was capable to effectively separate oil/water mixtures in a broad pH range or with a high concentration of salt, suggesting that this membrane was quite promising for future real-world practice in oil spill cleanup and oily wastewater treatment.

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Nanofibrous scaffolds from cotton cellulose and nano-hydroxyapatite (nano-HA) were electrospun for bone tissue engineering. The solution properties of cellulose/nano-HA spinning dopes and their associated electrospinnability were characterized. Morphological, thermal and mechanical properties of the electrospun cellulose/nano-HA nanocomposite nanofibers (ECHNN) were measured and the biocompatibility of ECHNN with human dental follicle cells (HDFCs) was evaluated. Scanning electron microscope (SEM) images indicated that the average diameter of ECHNN increased with a higher nano-HA loading and the fiber diameter distributions were well within the range of natural ECM (extra cellular matrix) fibers (50-500nm). The ECHNN exhibited extraordinary mechanical properties with a tensile strength and a Young's modulus up to 70.6MPa and 3.12GPa respectively. Moreover, it was discovered that the thermostability of the ECHNN could be enhanced with the incorporation of nano-HA. Cell culture experiments demonstrated that the ECHNN scaffolds were quite biocompatible for HDFCs attachment and proliferation, suggesting their great potentials as scaffold materials in bone tissue engineering.

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