Efficient preparation of anisotropic cellulose sponge from cotton stalks: An excellent material for separation applications.

Water pollution and solid waste resource reuse demand immediate attention and research. Here, we present a method to create anisotropic cellulose sponges from cotton stalk waste. Using the inherent structure of cotton stalks, we selectively remove lignin and hemicellulose via acid and alkali pretreatment. This process yields cellulose sponges with a natural pore structure. Our findings demonstrate that these sponges retain the original pore configuration of cotton stalks, providing excellent connectivity and compressibility due to their unique anisotropic three-dimensional structure. Moreover, these sponges exhibit exceptional super-hydrophilic and underwater super-oleophobic properties, with underwater oil contact angles exceeding 150° for all tested oils. External pressure can reduce the pore size of the cellulose sponge, facilitating the gravity-driven separation and removal of dyes and emulsions. Remarkably, removal efficiencies for Methylene Blue (MB), Congo Red (CR), water-in-oil (w/o) emulsions, and oil-in-water (o/w) emulsions exceed 99 %, 97 %, 99 %, and 99 %, respectively, highlighting superior removal and recyclability. Further investigation into the mechanisms of dye and emulsion removal employs X-ray photoelectron spectroscopy (XPS) characterization and molecular dynamics (MD) simulation. These insights lay the groundwork for the efficient recycling and resource utilization of waste cotton stalks, offering promising applications in water purification.

Fluorine-Functionalized Covalent Organic Framework Superhydrophobic Modified Melamine Sponge for Efficient oil-water Separation.

Hydrophobic sponges have attracted significant interest in oil spills and water-oil separation as potential absorption materials due to their desirable absorptivity, selectivity, and elasticity. In this paper, a hydrophilic melamine sponge (MS) is transferred into a superhydrophobic sponge via polydimethylsiloxane (PDMS) modification followed by in situ growth of fluorine-functionalized covalent organic framework (denoted as TFA-COF) nanoparticles. Therefore, the PDMS@TFA-COF@MS sponge was successfully prepared for efficient oil-water separation. The resultant PDMS@TFA-COF@MS exhibits superhydrophobic properties with a water contact angle of 156.7°. The superhydrophobic sponge has selectivity adsorption for different organic solvents and oils from water as well as oil-water separation efficiency (96% after 30 cycles) and oil absorption capacity (12 646% after 30 cycles). Meanwhile, the PDMS@TFA-COF@MS sponge exhibits strong thermal stability and flame retardancy in addition to having exceptional resistance to chemical corrosion in acidic, alkaline, and salt solutions. Moreover, the surfactant-stabilized oil-in-water emulsion could be efficiently separated by the sponge. Therefore, the prepared superhydrophobic PDMS@TFA-COF@MS sponge demonstrates possible uses for long-life oil-water separation applications.

Effect of Solvent Treatment on the Composition and Structure of Santanghu Long Flame Coal and Its Rapid Pyrolysis Products.

Easily soluble organic components in Santanghu long flame coal (SLFC) from Hami (Xinjiang, China) were separated by CS2 and acetone mixed solvent (v/v = 1:1) under ultrasonic condition, and the extract residue was stratified by carbon tetrachloride to obtain the light raffinate component (SLFC-L). The effect of solvent treatment on the composition and structure of the coal and its rapid pyrolysis products was analyzed. Solvent treatment can reduce the moisture content in coal from 9.48% to 6.45% and increase the volatile matter from 26.59% to 28.78%, while the macromolecular structure of the coal changed slightly, demonstrating the stability of coal's complex organic structure. Compared with raw coal, the relative contents of oxygen-containing functional groups and aromatic groups in SLFC-L are higher, and the weight loss rates of both SLFC and SLFC-L reached the maximum at about 450 °C. In contrast, the loss rate of SLFC-L is more obvious, being 33.62% higher than that of SLFC. Pyrolysis products from SLFC at 450 °C by Py-GC/MS are mainly aliphatic hydrocarbons and oxygenated compounds, and the relative contents of aliphatic hydrocarbons decreased from 48.48% to 36.13%, while the contents of oxygenates increased from 39.07% to 44.95%. Overall, the composition and functional group in the coal sample were changed after solvent treatment, resulting in a difference in the composition and distribution of its pyrolysis products.

The relationship between online learning self-efficacy, informal digital learning of English, and student engagement in online classes: the mediating role of social presence.

Introduction: This study investigates the interplay between Online Learning Self-Efficacy (OLSE), Informal Digital Learning of English (IDLE), student engagement in online classes, and the mediating effect of Social Presence (SP) among intermediate Chinese English as a Foreign Language (EFL) students. The research sample consisted of 389 participants enrolled in online English courses within a chain of language schools. Methods: Data collection involved the use of validated scales to assess OLSE, IDLE, SP, and online student engagement. Structural Equation Modeling (SEM) was employed for data analysis. Results: The findings revealed direct influences of OLSE and SP on online student engagement. Additionally, IDLE exhibited a positive impact on online student engagement, with a partial mediation effect through SP. This suggests that informal digital English learning significantly contributes to students' engagement in online classes, with this influence being facilitated by the sense of social presence experienced by students during virtual interactions. Discussion: This research underscores the importance of OLSE, IDLE, and SP in shaping student engagement within online learning environments. The results highlight that fostering informal digital English learning can enhance students' active participation in online courses, with SP serving as a key mediator in this relationship. These insights provide valuable guidance for educators and institutions seeking to improve student engagement in online educational settings.

Adsorption behavior of UV aged microplastics on the heavy metals Pb(II) and Cu(II) in aqueous solutions.

As the "vector" of heavy metals in the aquatic environment, microplastics (MPs) have a great influence on the migration and transformation of heavy metals. In this study, the adsorption of polypropylene (PP), polyethylene (PE) and polystyrene (PS) on two models of heavy metals after UV aging and environmental variables (ionic coexistence, pH, salinity, and fulvic acid) were comprehensively explored on adsorption. The results show that new oxidation functional groups are formed and their hydrophilicity is enhanced after MPs aging. As a result, the adsorption experiments showed that the adsorption of contaminants by UV aged MPs exceeds that of pristine MPs. The adsorption amounts of Pb(II) and Cu(II) by PP, PE and PS increased by 1.45, 1.46, 1.25 and 1.63, 1.39, 1.22 times, respectively. Adsorption kinetic data were more consistent with the pseudo-second-order kinetic model, proving chemisorption to be the mechanism governing the interaction between metal ions and MPs. The Freundlich model could accurately predict the heavy metal adsorption isotherms on MPs, showing that non-homogeneous multilayer adsorption dominates the process. In Pb(II)-Cu(II) binary composite system, metal ion adsorption capacity on MPs is less than that of the single system adsorption capacity, which proves that there is a specific inhibitory effect between coexisting ions. Additionally, external factors like pH, salinity, and fulvic acid content have a big impact on adsorption behavior. According to mechanism analysis, the adsorption process mainly relies on electrostatic interaction, surface complexation, and van der Waals force.

UV and chemical aging alter the adsorption behavior of microplastics for tetracycline.

This study evaluates the "vector" effects of different microplastics (MPs) on coexisting pollutants. The adsorption of tetracycline was studied on biodegradable plastics poly(butylene adipate-co-terephthalate) (PBAT) and non-biodegradable plastics polystyrene (PS), polypropylene (PP), and polyethylene (PE) after UV aging and chemical aging. The physicochemical properties of PBAT changed more obviously after UV radiation and chemical aging comparing to PS, PP and PE. Pores and cracks appear on the surface of aged PBAT. The crystallinity increased from 29.2% to 52.62%. In adsorption experiments, pristine and aged PBAT had strong vector effects on the adsorption of tetracycline than PS, PP and PE. The adsorption capacity of tetracycline on PBAT was increased from 0.7980 mg g-1 to 1.2669 mg g-1 after chemical aging. The adsorption mechanism indicated that electrostatic interactions and hydrogen bonds contribute to the adsorption process. In addition, for the adsorption of tetracycline on PS, π-π interaction was the main cause, and the adsorption mechanism was not considerably changed by aging. In conclusion, this study demonstrates that biodegradable plastics have substantial vector effect on coexisting pollutants at the end of their life cycle, this contributes to assessment of the risk from microplastic pollution.

Design of choline chloride modified USY zeolites for palladium-catalyzed acetylene hydrochlorination.

USY zeolites (USY) were applied to design and synthesize palladium-based heterogeneous catalysts for exploring an efficient non-mercuric catalyst for acetylene hydrochlorination. Choline chloride (ChCl) was selected as the nitrogen-containing ligand to modify the Pd@USY catalysts and the proposed Pd@15ChCl@USY catalyst exhibited obviously the best catalytic performance with a stable acetylene conversion and vinyl chloride selectivity of over 99.0% for more than 20 h. According to the results of characterization and the density functional theory calculations, it is indicated that the addition of ChCl can significantly inhibit the agglomeration and loss of the Pd active species, prevent carbon deposition and enhance the ability of HCl and C2H2 adsorption and C2H3Cl desorption, resulting in promoting the catalytic performance of Pd@USY catalysts during the acetylene hydrochlorination reaction.

Urchin-like hybrid nanostructures of CuOx/Fe2O3 from Cu-mediated pyrolysis of Fe-MOFs for catalytic reduction of organic pollutants.

MOFs have been widely used as templates to design and construct catalysis materials, such as LDH, metal oxides, and carbon. Herein, we developed a Cu-mediated pyrolysis protocol for the synthesis of urchin-like CuOx/Fe2O3 hybrid nanostructures using Fe-MOFs as the precursor. The hierarchical hybrids were composed of an inner CuOx-dispersed Fe2O3 octahedral matrix covered with radially grown Fe2O3 nanorods. This novel hierarchical hybrid nanostructure was generated likely due to the difference in the inward contraction rates between the Cu and Fe species during pyrolysis. Given the structural and compositional benefits, the urchin-like CuOx/Fe2O3 hybrids exhibited outstanding catalytic activity for the chemical reduction of 4-nitrophenol (4-NP) and dyes. Besides, CuOx/Fe2O3 was found to be highly catalytic in the reduction of 4-NP even after 30 consecutive runs, manifesting outstanding durability for continuous operation.

In situ construction of sulfated TiO2 nanoparticles with TiOSO4 for enhanced photocatalytic hydrogen production.

Photocatalytic hydrogen production from water is a promising method to obtain clean energy in the future. In this work, the sulfated TiO2 photocatalyst is successfully constructed in situ via a soft-templated method for photocatalytic water splitting to produce hydrogen. The content of sulfate species in TiO2 can be tuned by changing the amount of the surfactant. The photocatalyst with the appropriate content of sulfate ions exhibits an apparent quantum efficiency (AQE) of 3.9% at 365 nm and a high hydrogen production rate of 24.32 mmol h-1 g-1, which is 1.65 times that of commercial TiO2 (P25). The optimized photocatalyst has excellent photocatalytic activity for hydrogen evolution benefitting from the presence of sulfate ions on the surface of TiO2, large surface area and oxygen vacancies, which facilitates the rapid migration of photo-generated electrons to its surface and the improvement of the separation efficiency of photo-generated carriers. This work may inspire the rational design and the development of high-efficiency photocatalysts.

TiO2/Fe2O3 heterostructures with enhanced photocatalytic reduction of Cr(vi) under visible light irradiation.

We report a study on the synthesis of TiO2/Fe2O3 (TF) nanocomposites and their photocatalytic performance under visible-light irradiation. The characterization of structure and morphology shows that hematite Fe2O3 was deposited on anatase TiO2 nanoparticles with particle sizes in the range of 20-100 nm. In contrast to pure TiO2 and pure Fe2O3, the nanocomposites exhibited remarkable photocatalytic activity. For example, the photoreduction efficiency of TF0.5 reaches 100% for a 100 ppm Cr(vi) solution within 160 minutes. The photochemical properties were studied by various methods. Finally, we conclude that the excellent performance of the photocatalysts is mainly attributed to two aspects: the enhanced absorption of visible light and the synergistic effect of an internal electric field at the heterojunction and citric acid for promoting the separation of electron-hole pairs.

Underwater superoleophobic polyurethane-coated mesh with excellent stability for oil/water separation.

Oil/water separation has been a challenge in chemical engineering for various applications. There are numbers of studies on using coated metal meshes as a filter for oil/water separation. However, water resistance, chemical (such as: acid, base, and fouling) resistance and heat resistance for coating materials need further exploration, especially in terms of the durability of the coating materials. In this study, we synthesized a new coating material, hydrophilic polycarbonate polyurethane (HPCPU). We used HPCPU to chemically modify a steel mesh, and the mesh exhibits superhydrophilic and underwater superoleophobic properties. The HPCPU coated mesh shows excellent capacity for oil/water separation with a separation efficiency higher than 99.99% even after 40 cycles of separation. The coating material also exhibits excellent properties of water resistance, heat resistance, and chemical resistance. Moreover, the HPCPU-coated mesh exhibits a strong durability. For example, the separation efficiency for various oil/water mixtures remains higher than 99.7% after the HPCPU-coated mesh has been soaked in water for 30 days, hot water for 5 days, oils for 5 days, 0.5 M HCl solution, 0.5 M NaOH solution and 0.5 M NaCl solution for 24 hours.

Electric field-induced gradient strength in nanocomposite hydrogel through gradient crosslinking of clay.

In this paper, mechanically strong organic-inorganic nanocomposite (NC) gradient hydrogels were successfully prepared by the in situ polymerization of acrylamide (Am) and N,N-dimethyl aminoethyl methacrylate (DMAEMA) using an electrophoresis method. Due to its specific colloidal properties, LAPONITE® showed directional movement in direct-current (DC) electric field and thus formed a gradient distribution in the hydrogel. The concentration gradient of LAPONITE® was characterized by UV-vis absorption, FTIR and TGA. The network structures of lyophilized gradient hydrogels were observed from SEM images. The TEM morphology indicated that LAPONITE® had a good gradient dispersion in the NC gradient hydrogel. As a physical crosslinker, LAPONITE® can regulate the cross-linking density of the hydrogel, thus affecting its mechanical properties. The NC gradient hydrogel exhibited a high mechanical strength (a gradient tensile strength ranging from 43.4 to 135.3 kPa and a gradient compression strength ranging from 116 kPa to 1100 kPa, depending on the distance from the anode). This work provided a facile method to develop NC gradient hydrogels with improved mechanical performance. The NC gradient hydrogels can be used as potential candidates in the field of biological and chemical materials.

Green composite films prepared from cellulose, starch and lignin in room-temperature ionic liquid.

A series of novel biobased composite films derived from cellulose, starch and lignin were prepared from an ionic liquid (IL), 1-allyl-3-methylimidazolium chloride (AmimCl) by coagulating in a nonsolvent condition. The ionic liquid can be recycled with a high yield and purity after the green film was prepared. The uniform design method was applied to investigate mechanical properties of the biobased composite films. The effect of each component and their associated interactive effects were investigated. The experimental results showed that contents of cellulose, lignin and starch had a significant influence on the mechanical properties of composite films. The composite films showed relatively excellent mechanical properties in dry and wet states owing to the mutual property supplement of different components. The composite films were characterized via FT-IR, X-ray diffraction (XRD) and scanning electron microscope (SEM). Their thermal stability and gas permeability were also investigated, and the results showed that the composite films had good thermal stability and high gas barrier capacity and give a CO(2):O(2) permeability ratio close to 1.