Attuning doped ZnO-based composites for an effective light-driven mineralization of pharmaceuticals via PMS activation.

Water treatment technologies need to go beyond the current control of organic contaminants and ensure access to potable water. However, existing methods are still costly and often inadequate. In this context, novel catalysts that improve the mineralization degree of a wider range of pharmaceuticals through more benign and less consuming methodologies are highly sought after. ZnO, especially when doped, is a well-known semiconductor that also excels in the photocatalytic removal of persistent organic pollutants. In this study, we investigated the effect of doping ZnO nanoparticles with either copper, gallium or indium on the structure, morphology, photophysical properties and photocatalytic mineralization of pharmaceuticals. Their architecture was further improved through the fabrication of composites, pairing the best performing doped ZnO with either BaFe12O19 or nickel nanoparticles. Their suitability was tested on a complex 60-ppm multi-pollutant solution (tetracycline, levofloxacin and lansoprazole). The activation strategy combined photocatalysis with peroxymonosulfate (PMS) as an environmentally friendly source of highly oxidative sulfate radicals. The alliance of doped ZnO and BaFe12O19 was particularly successful, resulting in magnetic microcroquette-shaped composites with excellent inter-component synergy. In fact, indium outperformed the other proposed metal dopants, exceeding 97% mineralization after 1 h and achieving complete elimination after 3 h. All composites excelled in terms of reusability, with no catalytic loss after 10 consecutive cycles and minimal leakage of metal ions, highlighting their applicability in water remediation.

Study of Electrical and Dielectric Behaviors of Copper-Doped Zinc Oxide Ceramic Prepared by Spark Plasma Sintering for Electronic Device Applications.

In this study, Cu-doped ZnO aerogel nanoparticles with a 4% copper concentration (Cu4ZO) were synthesized using a sol-gel method, followed by supercritical drying and heat treatment. The subsequent fabrication of Cu4ZO ceramics through Spark Plasma Sintering (SPS) was characterized by X-ray diffraction (XRD), field-emission gun scanning electron microscopy (FE-SEM) equipped with EDS, and impedance spectroscopy (IS) across a frequency range of 100 Hz to 1 MHz and temperatures from 270 K to 370 K. The SPS-Cu4ZO sample exhibited a hexagonal wurtzite structure with an average crystallite size of approximately 229 ± 10 nm, showcasing a compact structure with discernible pores. The EDS spectrum indicates the presence of the base elements zinc and oxygen with copper like the dopant element. Remarkably, the material displayed distinct electrical properties, featuring high activation energy values of about 0.269 ± 0.021 eV. Complex impedance spectroscopy revealed the impact of temperature on electrical relaxation phenomena, with the Nyquist plot indicating semicircular arc patterns associated with grain boundaries. As temperature increased, a noticeable reduction in the radius of these arcs occurred, coupled with a shift in their center points toward the axis center, suggesting a non-Debye-type relaxation mechanism. Dielectric analyses revealed a temperature-driven evolution of losses, emphasizing the material's conductivity impact. Non-Debye-type behavior, linked to ion diffusion, sheds light on charge storage dynamics. These insights advance potential applications in electronic devices and energy storage.

Advanced degradation of organic pollutants using sonophotocatalytic peroxymonosulfate activation with CoFe2O4/Cu- and Ce-doped SnO2 composites.

The rampant upsurge of organic pollutants in aqueous media has become one of the major concerns nowadays. Finding non-specific catalysts that can target a wide range of organic pollutants is a key challenge. Eco-friendly oxidative radicals, such as promoted by peroxymonosulfate (PMS), are necessary for efficient water decontamination. We propose a multicomponent composite catalyst for activating PMS using a dual strategy of sonophotocatalysis. The composite integrates cobalt ferrite and Cu- or Ce-doped SnO2, with the at. % of doping metal and the mixture ratio carefully balanced. The top-performing architectures were able to decompose rhodamine B (20 ppm), a representative pollutant, in under 3 min and achieve over 70% mineralization in just 5 min. The synthesized nanocomposites demonstrated exceptional sonophotocatalytic performance, even when treating complex and diverse multipollutant solutions (80 ppm), achieving over 75% mineralization after 150 min. Considering their high stability and reusability, the proposed CoFe2O4/Cu- and Ce-doped SnO2 materials are among the state-of-the-art heterogeneous catalysts for mineralizing organic pollutants through PMS activation.

Validation of a 3D Local-Scale Adaptive Solar Radiation Model by Using Pyranometer Measurements and a High-Resolution Digital Elevation Model.

The result of the multidisciplinary collaboration of researchers from different areas of knowledge to validate a solar radiation model is presented. The MAPsol is a 3D local-scale adaptive solar radiation model that allows us to estimate direct, diffuse, and reflected irradiance for clear sky conditions. The model includes the adaptation of the mesh to complex orography and albedo, and considers the shadows cast by the terrain and buildings. The surface mesh generation is based on surface refinement, smoothing and parameterization techniques and allows the generation of high-quality adapted meshes with a reasonable number of elements. Another key aspect of the paper is the generation of a high-resolution digital elevation model (DEM). This high-resolution DEM is constructed from LiDAR data, and its resolution is two times more accurate than the publicly available DEMs. The validation process uses direct and global solar irradiance data obtained from pyranometers at the University of Salamanca located in an urban area affected by systematic shading from nearby buildings. This work provides an efficient protocol for studying solar resources, with particular emphasis on areas of complex orography and dense buildings where shadows can potentially make solar energy production facilities less efficient.

Fe/Au galvanic nanocells to generate self-sustained Fenton reactions without additives at neutral pH.

The generation of reactive oxygen species (ROS) via the Fenton reaction has received significant attention for widespread applications. This reaction can be triggered by zero-valent metal nanoparticles by converting externally added H2O2 into hydroxyl radicals (˙OH) in acidic media. To avoid the addition of external additives or energy supply, developing self-sustained catalytic systems enabling onsite production of H2O2 at a neutral pH is crucial. Here, we present novel galvanic nanocells (GNCs) based on metallic Fe/Au bilayers on arrays of nanoporous silica nanostructures for the generation of self-sustained Fenton reactions. These GNCs exploit the large electrochemical potential difference between the Fe and Au layers to enable direct H2O2 production and efficient release of Fe2+ in water at neutral pH, thereby triggering the Fenton reaction. Additionally, the GNCs promote Fe2+/Fe3+ circulation and minimize side reactions that passivate the iron surface to enhance their reactivity. The capability to directly trigger the Fenton reaction in water at pH 7 is demonstrated by the fast degradation and mineralization of organic pollutants, by using tiny amounts of catalyst. The self-generated H2O2 and its transformation into ˙OH in a neutral environment provide a promising route not only in environmental remediation but also to produce therapeutic ROS and address the limitations of Fenton catalytic nanostructures.

Enhanced Activation of Peroxymonosulfate for Tetracycline Degradation Using CoNi-Based Electrodeposited Films.

Synthesizing efficient heterogeneous catalysts with multiple active sites able to activate peroxymonosulfate (PMS) for the degradation of persistent organic pollutants continues to be a challenge for societies worldwide. In response, cost-effective, eco-friendly oxidized Ni-rich and Co-rich CoNi micro-nanostructured films were fabricated following a two-step process based on simple electrodeposition using green deep eutectic solvent as an electrochemical media and thermal annealing. The CoNi-based catalysts demonstrated exceptional efficiency in the heterogeneous catalyzed activation of PMS for tetracycline degradation and mineralization. The effects of the catalysts' chemical nature and morphology, the pH, the concentration of PMS, irradiation with visible light, and the duration of contact with the catalysts on the degradation and mineralization of tetracycline were also studied. In dark conditions, oxidized Co-rich CoNi degraded more than 99% of tetracyclines in only 30 min and mineralized more than 99% of them in only 60 min. Moreover, the degradation kinetics doubled from 0.173 min-1 in dark conditions to 0.388 min-1 under visible light irradiation. In addition, the material demonstrated excellent reusability and can be easily recovered with simple heat treatment. Given those findings, our work provides new strategies for constructing high-efficiency and cost-effective PMS catalysts and elucidating the effects of operational parameters and primary reactive species formed by the catalyst-PMS system on water treatment technologies.

Scalable Microfabrication of Multi-Emitter Arrays in Silicon for a Compact Microfluidic Electrospray Propulsion System.

The recent proliferation of SmallSats and their use in increasingly demanding applications require the development of onboard electric propulsion compatible with the power, mass, and volume constraints of these spacecraft. Electrospray propulsion is a promising technology for SmallSats due to its unique high efficiency and scalability across the wide power range of these platforms, for example, from a few watts available in a CubeSat to a few hundred watts in a MiniSat. The implementation of electrospray propulsion requires the use of microfabrication techniques to create compact arrays of thousands of electrospray emitters. This article demonstrates the microfabrication of multi-emitter electrospray sources of a scalable size for electrospray propulsion. In particular, a microfabrication and assembly process is developed and demonstrated by fabricating sources with arrays of 1, 64, and 256 emitters. The electrospray sources are tested in a relevant environment for space propulsion (inside a vacuum chamber), exhibiting excellent propulsive performance (e.g., absence of beam impingement in the extractor electrode, absence of hysteresis in the beam current versus propellant flow rate characteristic, proper operation in the cone-jet electrospraying mode, etc.) and nearly coincident output per emitter. Several design elements contribute to this performance: the even distribution of the propellant among all emitters made possible by the implementation of a network of microfluidic channels in the backside of the emitter array; the small dead volume of the network of microfluidic channels; the accurate alignment between the emitters and extractor orifices; and the use of a pipe-flow configuration to drive the propellant through closed conduits, which protects the propellant.

Utilizing Biomass-Based Graphene Oxide-Polyaniline-Ag Electrodes in Microbial Fuel Cells to Boost Energy Generation and Heavy Metal Removal.

Although regarded as environmentally stable, bioelectrochemical fuel cells or, microbial fuel cells (MFCs) continue to face challenges with sustaining electron transport. In response, we examined the performance of two graphene composite-based anode electrodes-graphene oxide (GO) and GO-polymer-metal oxide (GO-PANI-Ag)-prepared from biomass and used in MFCs. Over 7 days of operation, GO energy efficiency peaked at 1.022 mW/m2 and GO-PANI-Ag at 2.09 mW/m2. We also tested how well the MFCs could remove heavy metal ions from synthetic wastewater, a secondary application of MFCs that offers considerable benefits. Overall, GO-PANI-Ag had a higher removal rate than GO, with 78.10% removal of Pb(II) and 80.25% removal of Cd(II). Material characterizations, electrochemical testing, and microbial testing conducted to validate the anodes performance confirmed that using new materials as electrodes in MFCs can be an attractive approach to improve the electron transportation. When used with a natural organic substrate (e.g., sugar cane juice), they also present fewer challenges. We also optimized different parameters to confirm the efficiency of the MFCs under various operating conditions. Considering those results, we discuss some lingering challenges and potential possibilities for MFCs.

Utilization of lignocellulosic biomass: A practical journey towards the development of emulsifying agent.

With each passing year, the agriculture and wood processing industries generate increasingly high tonnages of biomass waste, which instead of being burned or left to accumulate should be utilized more sustainably. In parallel, advances in green technology have encouraged large companies and nations to begin using eco-friendly materials, including eco-friendly emulsifiers, which are used in various industries and in bio-based materials. The emulsion-conducive properties of lignocellulosic materials such as cellulose, hemicellulose, and lignin, the building blocks of plant and wood structures, have demonstrated a particular ability to alter the landscape of emulsion technology. Beyond that, the further modification of their structure may improve emulsion stability, which often determines the performance of emulsions. Considering those trends, this review examines the performance of lignocellulosic materials after modification according to their stability, droplet size, and distribution by size, all of which suggest their outstanding potential as materials for emulsifying agents.

Exploring the Potential of Cotton Industry Byproducts in the Plastic Composite Sector: Macro and Micromechanics Study of the Flexural Modulus.

The textile sector produces yearly great quantities of cotton byproducts, and the major part is either incinerated or landfilled, resulting in serious environmental risks. The use of such byproducts in the composite sector presents an attractive opportunity to valorize the residue, reduce its environmental impact, and decrease the pressure on natural and synthetic resources. In this work, composite materials based on polypropylene and dyed cotton byproducts from the textile industry were manufactured. The competitiveness of the resulting composites was evaluated from the analyses, at macro and micro scales, of the flexural modulus. It was observed that the presence of dyes in cotton fibers, also a byproduct from the production of denim items, notably favored the dispersion of the phases in comparison with other cellulose-rich fibers. Further, the presence of a coupling agent, in this case, maleic anhydride grafted polypropylene, enhanced the interfacial adhesion of the composite. As a result, the flexural modulus of the composite at 50 wt.% of cotton fibers enhanced by 272% the modulus of the matrix. From the micromechanics analysis, using the Hirsch model, the intrinsic flexural modulus of cotton fibers was set at 20.9 GPa. Other relevant micromechanics factors were studied to evaluate the contribution and efficiency of the fibers to the flexural modulus of the composite. Overall, the work sheds light on the potential of cotton industry byproducts to contribute to a circular economy.

Removal of Cyanobacteria and Cyanotoxins in Waters.

Harmful cyanobacterial algal blooms and cyanotoxins currently pose a major threat to global society, one that exceeds local and national interests due to their extremely destructive effects on the environment and human health [...].

Assessing the Chemical Stability and Cytotoxicity of Electrodeposited Magnetic Mesoporous Fe-Pt Films for Biomedical Applications.

The development of feasible micro/nanoplatforms for various biomedical applications requires holistic research that explores scalable synthesis and design pathways and imposes an interdisciplinary integration of materials science, physical, medical, chemical, and biological knowledge. Thanks to their unique characteristics (i.e., structure, large specific surface areas, tuneability, versatility, and integrity), mesoporous materials have emerged as potential candidates for being part of micro/nanoplatforms for therapeutic, monitoring, and diagnostic applications. In this context, Fe-Pt mesoporous materials are excellent candidates to be part of biomedical micro/nanoplatforms, thanks to their chemical nature, structure, and magnetic properties, which endow them with magnetic locomotion, high cargo capability of therapeutic agents inside the mesoporous cavity, and large surface area for surface functionalization. However, the chemical stability in biological media and cytotoxicity of the Fe-Pt mesoporous material (without considering the effects of architecture and shape) are pivotal elements that determine the suitability of these materials for biomedical applications. This work demonstrates the following: (i) the potential of electrochemical deposition, based on the use of block copolymer micellar solutions as electrochemical media, as an easy, inexpensive, and scalable strategy to synthesize mesoporous Fe-Pt components with tunable chemical composition, porosity, magnetism, and shape (in this case films, but other architectures like nanowires can be easily fabricated using simultaneously hard templates); (ii) the excellent corrosion stability, which is comparable to bulk Au, and minimal chemical dissolution in biological media after 160 h of immersion (∼0.88% of Fe and ∼0.0019% of Pt), which confirms the robustness of Fe-Pt; and (iii) negligible cytotoxicity on HaCaT cells (human immortalized keratinocytes), which reinforces the biocompatibility of Fe-Pt mesoporous structures. Also, the presence of Fe-Pt mesoporous films seems to induce a slight increase in cell viability. These results confirm the biocompatibility of Fe-Pt mesoporous films, making them suitable for biomedical applications.

Electrodeposited Ni-Rich Ni-Pt Mesoporous Nanowires for Selective and Efficient Formic Acid-Assisted Hydrogenation of Levulinic Acid to γ-Valerolactone.

In pursuit of friendlier conditions for the preparation of high-value biochemicals, we developed catalytic synthesis of γ-valerolactone by levulinic acid hydrogenation with formic acid as the hydrogen source. Both levulinic and formic acid are intermediate products in the biomass transformation processes. The objective of the work is twofold: the development of a novel approach for milder synthesis conditions to produce γ-valerolactone and the reduction of the economic cost of the catalyst. Ni-rich Ni-Pt mesoporous nanowires were synthesized in an aqueous medium using a combined hard-soft-template-assisted electrodeposition method, in which porous polycarbonate membranes controlled the shape and the Pluronic P-123 copolymer served as the porogen agent. The electrodeposition conditions selected favored nickel deposition and generated nanowires with nickel percentages above 75 atom %. The increase in deposition potential favored nickel deposition. However, it was detrimental for the porous diameter because the mesoporous structure is promoted by the presence of the platinum-rich micelles near the substrate, which is not favored at more negative potentials. The prepared catalysts promoted the complete transformation to γ-valerolactone in a yield of around 99% and proceeded with the absence of byproducts. The coupling temperature and reaction time were optimized considering the energy cost. The threshold operational temperature was established at 140 °C, at which, 120 min was sufficient for attaining the complete transformation. Working temperatures below 140 °C rendered the reaction completion difficult. The Ni78Pt22 nanowires exhibited excellent reusability, with minimal nickel leaching into the reaction mixture, whereas those with higher nickel contents showed corrosion.

Enhanced Photocatalytic Removal of Cyanotoxins by Al-Doped ZnO Nanoparticles with Visible-LED Irradiation.

The ZnO-based visible-LED photocatalytic degradation and mineralization of two typical cyanotoxins, microcystin-LR (MC-LR), and anatoxin-A were examined. Al-doped ZnO nanoparticle photocatalysts, in Al:Zn ratios between 0 and 5 at.%, were prepared via sol-gel method and exhaustively characterized by X-ray diffraction, transmission electron microscopy, UV-vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, and nitrogen adsorption-desorption isotherms. With both cyanotoxins, increasing the Al content enhances the degradation kinetics, hence the use of nanoparticles with 5 at.% Al content (A5ZO). The dosage affected both cyanotoxins similarly, and the photocatalytic degradation kinetics improved with photocatalyst concentrations between 0.5 and 1.0 g L-1. Nevertheless, the pH study revealed that the chemical state of a species decisively facilitates the mutual interaction of cyanotoxin and photocatalysts. A5ZO nanoparticles achieved better outcomes than other photocatalysts to date, and after 180 min, the mineralization of anatoxin-A was virtually complete in weak alkaline medium, whereas only 45% of MC-LR was in neutral conditions. Moreover, photocatalyst reusability is clear for anatoxin-A, but it is adversely affected for MC-LR.

Photocatalytic treatment of natural waters. Reality or hype? The case of cyanotoxins remediation.

This review compiles recent advances and challenges in the photocatalytic treatment of natural water by analyzing the remediation of cyanotoxins. The review frames the treatment need based on the occurrence, geographical distribution, and legislation of cyanotoxins in drinking water while highlighting the underestimated global risk of cyanotoxins. Next, the fundamental principles of photocatalytic treatment for remediating cyanotoxins and the complex degradation pathway for the most widespread cyanotoxins are presented. The state-of-the-art and recent advances on photocatalytic treatment processes are critically discussed, especially the modification strategies involving TiO2 and the primary operational conditions that determine the scalability and integration of photocatalytic reactors. The relevance of light sources and light delivery strategies are shown, with emphasis on novel biomimicry materials design. Thereafter, the seldomly-addressed role of water-matrix components is thoroughly and critically explored by including natural organic matter and inorganic species to provide future directions in designing highly efficient strategies and scalable reactors.

Electrodeposition of Mesoporous Ni-Rich Ni-Pt Films for Highly Efficient Methanol Oxidation.

The use of soft templates for the electrosynthesis of mesoporous materials has shown tremendous potential in energy and environmental domains. Among all the approaches that have been featured in the literature, block copolymer-templated electrodeposition had robustness and a simple method, but it practically cannot be used for the synthesis of mesoporous materials not based on Pt or Au. Nonetheless, extending and understanding the possibilities and limitations of block copolymer-templated electrodeposition to other materials and substrates is still challenging. Herein, a critical analysis of the role of the solution's primary electroactive components and the applied potential were performed in order to understand their influences on the mesostructure of Ni-rich Ni-Pt mesoporous films. Among all the components, tetrahydrofuran and a platinum (IV) complex were shown to be crucial for the formation of a truly 3D mesoporous network. The electrosynthesized well-ordered mesoporous Ni-rich Ni-Pt deposits exhibit excellent electrocatalytic performance for methanol oxidation in alkaline conditions, improved stability and durability after 1000 cycles, and minimal CO poisoning.

Advances and Challenges in Developing Efficient Graphene Oxide-Based ZnO Photocatalysts for Dye Photo-Oxidation.

The efficient remediation of organic dyes from wastewater is increasingly valuable in water treatment technology, largely owing to the tons of hazardous chemicals currently and constantly released into rivers and seas from various industries, including the paper, pharmaceutical, textile, and dye production industries. Using solar energy as an inexhaustible source, photocatalysis ranks among the most promising wastewater treatment techniques for eliminating persistent organic pollutants and new emerging contaminants. In that context, developing efficient photocatalysts using sunlight irradiation and effectively integrating them into reactors, however, pose major challenges in the technologically relevant application of photocatalysts. As a potential solution, graphene oxide (GO)-based zinc oxide (ZnO) nanocomposites may be used together with different components (i.e., ZnO and GO-based materials) to overcome the drawbacks of ZnO photocatalysts. Indeed, mounting evidence suggests that using GO-based ZnO nanocomposites can promote light absorption, charge separation, charge transportation, and photo-oxidation of dyes. Despite such advances, viable, low-cost GO-based ZnO nanocomposite photocatalysts with sufficient efficiency, stability, and photostability remain to be developed, especially ones that can be integrated into photocatalytic reactors. This article offers a concise overview of state-of-the-art GO-based ZnO nanocomposites and the principal challenges in developing them.

Hybrid Ni@ZnO@ZnS-Microalgae for Circular Economy: A Smart Route to the Efficient Integration of Solar Photocatalytic Water Decontamination and Bioethanol Production.

Water remediation and development of carbon-neutral fuels are a priority for the evermore industrialized society. The answer to these challenges should be simple, sustainable, and inexpensive. Thus, biomimetic-inspired circular and holistic processes combing water remediation and biofuel production can be an appealing concept to deal with these global issues. A simple circular approach using helical Spirulina platensis microalgae as biotemplates to synthesize Ni@ZnO@ZnS photocatalysts for efficient solar water decontamination and bioethanol production during the recycling process is presented. Under solar irradiation, the Ni@ZnO@ZnS-Spirulina photocatalyst exhibits enhanced activity (mineralization efficiency >99%) with minimal photocorrosion and excellent reusability. At the end of its effective lifetime for water remediation, the microalgae skeleton (mainly glycogen and glucose) of the photocatalyst is recycled to directly produce bioethanol by simultaneous saccharification and fermentation process. An outstanding ethanol yield of 0.4 L kg-1, which is similar to the highest yield obtained from oxygenic photosynthetic microorganisms, is obtained. Thus, the entire process allows effective solar photocatalytic water remediation and bioethanol production at room temperature using simple and easily scalable procedures that simultaneously fixes carbon dioxide, thereby constituting a zero-carbon-emission circular process.

Highly reduced ecotoxicity of ZnO-based micro/nanostructures on aquatic biota: Influence of architecture, chemical composition, fixation, and photocatalytic efficiency.

Developing efficient sunlight photocatalysts with enhanced photocorrosion resistance and minimal ecotoxicological effects on aquatic biota is critical to combat water contamination. Here, the role of chemical composition, architecture, and fixation on the ecotoxicological effects on microalgae of different ZnO and ZnO@ZnS based water decontamination photocatalysts was analyzed in depth. In particular, the ecotoxicological effects of films, nanoparticles and biomimetic micro/nano-ferns were carefully assessed by correlating the algae's viability to the Zn(II) release, the photocatalyst-microalgae interaction, and the production of reactive oxygen species (ROS). The results showed a drastic improvement in algal viability for supported ZnO@ZnS core@shell micro/nanoferns, as their ecotoxicity after 96 h light exposure was significantly lower (3.7-10.0% viability loss) compared to the ZnO films (18.4-35.5% loss), ZnO micro/nanoferns (28.5-53.5% loss), ZnO nanoparticles (48.3-91.7% loss) or ZnO@ZnS nanoparticles (8.6-19.2% loss) for catalysts concentrations ranging from 25 mg L-1 to 400 mg L-1. In particular, the ZnO@ZnS micro/nanoferns with a concentration of 400 mg L-1 exhibited excellent photocatalytic efficiency to mineralize a multi-pollutant solution (81.4 ±â€¯0.3% mineralization efficiency after 210 min under UV-filtered visible light irradiation) and minimal photocorrosion (<5% of photocatalyst dissolution after 96 h of UV-filtered visible light irradiation). Remarkably, the ZnO@ZnS micro/nanoferns showed lower loss of algal viability (9.8 ±â€¯1.1%) after 96 h of light exposure, with minimal reduction in microalgal biomass (9.1 ±â€¯1.0%), as well as in the quantity of chlorophyll-a (9.5 ±â€¯1.0%), carotenoids (8.6 ±â€¯0.9%) and phycocyanin (5.6 ±â€¯0.6%). Altogether, the optimized ZnO@ZnS core@shell micro/nanoferns represent excellent ecofriendly photocatalysts for water remediation in complex media, as they combine enhanced sunlight remediation efficiency, minimal adverse effects on biological microorganisms, high reusability and easy recyclability.

Xyloglucan coating for enhanced strength and toughness in wood fibre networks.

In recent times, cellulosic materials are witnessing strong interest from both industry and academia for their ability to progress in high-value products with green stamp. Besides the renewability and biodegradability appeal, exceptional properties such as mechanical strength together with toughness are pursued. In the present work, wood fibre networks from eucalyptus Kraft pulp fibres and cellulose nanofibres are combined to produce nanostructured composite networks with outstanding mechanical behaviour. For this purpose, xyloglucan (XG) polymer is adsorbed on cellulose nanofibres (CNF) forming core-shell CNF fibrils in hydrocolloidal suspension which is used to dramatically strengthen wood fibre networks. TEMPO-CNF at two different oxidation levels were coated with XG. The exceptional Young's modulus and tensile strength found for fibre networks with only 10 wt% CNF was attributed to the fibre-fibre bond strength with better homogeneous stress distribution at the micro/nano scale. The production, mechanical characterization and structure analysis of such bionanocomposites is here presented.