Search Results (27)

Sustainable binders are becoming decisive enabling materials for fiber-based packaging and cellulosic nonwovens because they govern strength, coating integrity, barrier performance, printability, wet durability, and end-of-life behavior. However, replacing fossil-derived latexes, fluorinated finishes, or persistent wet-strength systems with renewable alternatives is not a simple material substitution problem. This perspective argues that sustainable binders must be evaluated through an industrial lens that integrates performance, scalability, cost, process compatibility, food-contact safety, and recyclability. The discussion examines current binder limitations, emerging bio-based alternatives including starch, cellulose derivatives, nanocellulose, proteins, lignin, tannins, chitosan, hemicelluloses, and reactive green crosslinking systems, and the specific opportunity to move from bulk binder replacement toward engineered cellulose–cellulose junctions. Enzyme-assisted activation of cellulose surfaces, especially routes that generate controlled carboxyl and aldehyde functionality, is highlighted as a promising platform for low-energy bonding of recyclable all-cellulose webs when paired with rigorous spectroscopy, mechanical testing, and multiscale modeling. The central conclusion is that the next generation of sustainable binders will be selected not by renewable content alone, but by their ability to deliver reliable performance within high-throughput manufacturing and credible recovery pathways. Full article

Trifluoroacetic acid (TFA) is an ultrashort-chain perfluoroalkyl substance (PFAS) characterized by environmental persistence, water solubility, and a growing global presence, resulting primarily from the degradation of fluorinated compounds. Evidence suggests that plant-based foods may represent an underestimated exposure route, with wine emerging as a significant dietary source due to accumulation in soils, irrigation water, and plant uptake. This review provides an updated summary of the evidence on the environmental sources and temporal evolution of TFA in wine, its analytical detection, its contribution to dietary exposure, potential implications for human health, and current regulatory attention. A structured but non-systematic literature search was conducted using PubMed and Scopus, supplemented by European reports and monitoring data, and in accordance with SANRA guidelines. Evidence shows that TFA concentrations in wine derive from widespread environmental sources and have increased over time, from negligible levels before the 1970s to a marked increase in recent decades. Reported concentrations range from tens to several hundred µg/L, despite analytical challenges. Exposure estimates indicate that wine may contribute significantly to total dietary TFA intake in regular consumers. Although toxicological data suggest low acute toxicity, uncertainties remain regarding long-term exposure, and regulatory limits for TFA in foods and beverages are lacking. Full article

There is a strong and growing need for low environmental impact, fluorine-free finishes that deliver durable water repellency and stain resistance to leather while preserving its original appearance. This work successfully addresses this need by introducing a simple, robust, and scalable two-step coating strategy that endows leather surfaces with excellent hydrophobic and self-cleaning properties. The process relies on a straightforward spray application of functionalized silica nanoparticles followed by a hydrophobic silane, namely hexadecyltrimethoxysilane (HDTMS), enabling precise control over surface properties through the number of applied layers. Comprehensive characterization by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM–EDS) confirmed the effective formation and uniformity of the coating. Performance testing demonstrated excellent functional outcomes: the optimized coating achieved a water contact angle (WCA) of 128° and maintained values above 125° even after abrasion, highlighting its durability. Treated leather exhibited resistance to common liquid stains such as tea and coffee, maintaining a clean surface. These functional gains were achieved without compromising the leather’s natural look or soft feel, even after multiple coating cycles. This work delivers a fluorine-free solution offering an effective route to high-value water- and stain-resistant leather finishes that respect both environmental and aesthetic requirements. Full article

Plasma-enhanced atomic layer deposition (PEALD) is used to grow high-quality aluminum fluoride (AlF₃) antireflective coatings via a safe, HF-free route using trimethylaluminum and SF₆ plasma. In situ diagnostics reveal a reaction pathway mediated by a hydrogen-terminated fluorinated surface (s-FH). By systematically varying the plasma pulse duration, a critical process window is identified that balances efficient ligand removal against ion-induced structural damage. Within this optimized window, the films achieve ultra-low impurity levels and an atomically smooth morphology, increasing the optical transmittance of glass to (97.6 ± 0.5)%. This study establishes a clear link between fundamental plasma kinetics and functional optical performance, providing a robust, non-corrosive strategy for the rational design of metal–fluoride PEALD coatings. Full article

The increasing impact of global warming is predominantly driven by the extensive use of fossil fuels, which release significant amounts of greenhouse gases into the atmosphere. This has led to a critical need for alternative, sustainable energy sources that can mitigate environmental impacts. Photovoltaic technology has emerged as a promising solution by harnessing renewable energy from the sun, providing a clean and inexhaustible power source. Perovskite solar cells (PSCs) are a class of hybrid organic–inorganic solar cells that have recently attracted significant scientific attention due to their low cost, relatively high efficiency, low–temperature processing routes, and longer carrier lifetimes. These characteristics make them a viable alternative to traditional fossil fuels, reducing the carbon footprint and contributing to the fight against global warming. In this study, the SCAPS–1D numerical simulator was used in the computational analysis of a PSC device with the configuration FTO/ETL/BaZr(S_0.6Se_0.4)₃/HTL/Ir. Different hole transport layer (HTL) and electron transport layer (ETL) material were proposed and tested. The HTL materials included copper (I) oxide (Cu₂O), 2,2′,7,7′–Tetrakis(N,N–di–p–methoxyphenylamine)9,9′–spirobifluorene (spiro–OMETAD), and poly(3–hexylthiophene) (P₃HT), while the ETLs included cadmium suphide (CdS), zinc oxide (ZnO), and [6,6]–phenyl–C₆₁–butyric acid methyl ester (PCBM). Finally, BaZr(S_0.6Se_0.4)₃ was proposed as an absorber, and a fluorine–doped tin oxide glass substrate (FTO) was proposed as an anode. The metal back contact used was iridium. Photovoltaic parameters such as short circuit density (I_sc), open circuit voltage (V_oc), fill factor (FF), and power conversion efficiency (PCE) were used to evaluate the performance of the device. The initial simulated primary device with the configuration FTO/CdS/BaZr(S_0.6Se_0.4)₃/spiro–OMETAD/Ir gave a PCE of 5.75%. Upon testing different HTL materials, the best HTL was found to be Cu₂O, and the PCE improved to 9.91%. Thereafter, different ETLs were also inserted and tested, and the best ETL was established to be ZnO, with a PCE of 10.10%. Ultimately an optimized device with a configuration of FTO/ZnO/BaZr(S_0.6Se_0.4)₃/Cu₂O/Ir was achieved. The other photovoltaic parameters for the optimized device were as follows: FF = 31.93%, J_sc = 14.51 mA cm⁻², and V_oc = 2.18 V. The results of this study will promote the use of environmentally benign BaZr(S_0.6Se_0.4)₃–based absorber materials in PSCs for improved performance and commercialization. Full article

The interfacial polymerization of fluorine-containing polyarylates (F-PAR) represents an important synthetic route for advanced polymeric materials. This work presents a comprehensive mechanistic investigation through integrated kinetic analysis and macromolecular characterization. The polymerization for both F-PAR and its non-fluorinated analogue (M-PAR) follows a two-stage, second-order kinetic profile, with the F-PAR system exhibiting a lower initial rate constant. Kinetic modeling revealed a dynamic reaction locus, transitioning from the bulk organic phase to an indistinguishable regime. The fluorinated system exhibits distinct stage-dependent behavior: initial retardation due to fluorine-induced “nucleophilicity penalty” on bisphenol monomer followed by a kinetic crossover where the growth rate of F-PAR surpasses M-PAR through enhanced oligomer electrophilicity. The terminal stage reveals fundamental divergence, while flexible M-PAR chains sustain accelerated growth via efficient chain-chain coupling, rigid F-PAR chains reach a molecular weight plateau. The incorporation of fluorine enhances thermal stability and optical transparency due to the low polarizability of C-F bonds. This study provides a complete mechanistic roadmap of fluorine’s dynamic role in polymer architecture control. Full article

Silica-based multifunctional coatings hold great promise for applications in optical devices, lenses, and solar panels. Herein, we report a facile, low-temperature route to integrate super-hydrophobicity with high transparency and low haze. By precisely controlling particle gradation and applying fluorine passivation, a multi-scale structure with micro-scale uniformity and nano-scale asperity was constructed. This unique architecture, combined with low surface energy, effectively reduces light scattering and enhances air trapping. Consequently, the coated glass achieves a high optical transmittance of 95.24% with a low haze of 0.97%, alongside a water contact angle of 153° and a sliding angle of 3°. The coating also exhibits distinct anti-reflection (an improvement of ~5.0% relative to the bare substrate) and self-cleaning properties. Furthermore, it demonstrates impressive robustness and durability, withstanding extreme conditions including cryogenic temperatures (−50 °C), hygrothermal environments, and long-term outdoor exposure. This work demonstrates the versatile potential of our strategy for fabricating highly transparent and superhydrophobic surfaces. Full article

Carbon dioxide (CO₂) is the most significant anthropogenic greenhouse gas (GHG), accounting for approximately 81% of total emissions, with methane (CH₄), nitrous oxide (N₂O), and fluorinated gases contributing the remainder. Rising atmospheric CO₂ concentrations, driven primarily by fossil fuel combustion, industrial processes, and transportation, have surpassed the Earth’s natural sequestration capacity, intensifying climate change impacts. Carbon Capture, Utilization, and Storage (CCUS) offers a portfolio of solutions to mitigate these emissions, encompassing pre-combustion, post-combustion, oxy-fuel combustion, and direct air capture (DAC) technologies. This review synthesizes advancements in CO₂ capture materials including liquid absorbents (amines, amino acids, ionic liquids, hydroxides/carbonates), solid adsorbents (metal–organic frameworks, zeolites, carbon-based materials, metal oxides), hybrid sorbents, and emerging hydrogel-based systems and their integration with utilization and storage routes. Special emphasis is given to CO₂ mineralization using mine tailings, steel slag, fly ash, and bauxite residue, as well as biological mineralization employing carbonic anhydrase (CA) immobilized in hydrogels. The techno-economic performance of these pathways is compared, highlighting that while high-capacity sorbents offer scalability, hydrogels and biomineralization excel in low-temperature regeneration and integration with waste valorization. Challenges remain in cost reduction, material stability under industrial flue gas conditions, and integration with renewable energy systems. The review concludes that hybrid, cross-technology CCUS configurations combining complementary capture, utilization, and storage strategies will be essential to meeting 2030 and 2050 climate targets. Full article

Developing durable hydrophobic and oleophobic textiles using simple and environmentally responsible techniques remains a challenge. This study aimed to determine how the structure of organosilicon silanes—specifically the type of functional group (fluorinated alkyl, long alkyl, or benzyl group) and the presence of an ester linker formed via the thiol–Michael addition—affects the wetting behaviour of cotton fabrics. Five silanes were synthesized and applied using a mild pad–dry–cure silanization process. The modified fabrics were evaluated through water and oil contact angle (WCA, OCA) measurements, water absorption tests, droplet-stability analysis, and washing-durability assessment. All treated samples exhibited hydrophobicity, while the silane containing a C6 perfluoroalkyl chain provided both hydrophobic and oleophobic performance. This fabric showed a WCA of 152° and an OCA of 126° (hexadecane), which remained essentially unchanged after 10 washing cycles (153° and 126°, respectively). Water absorption decreased by 91%, and droplets remained stable for at least 30 min. SEM, and SEM-EDS confirmed the presence and uniform distribution of the silane coating. These results demonstrate that short-chain fluorinated silanes and long-chain alkyl silanes can form durable low-surface-energy layers on cotton using a straightforward and efficient process, offering a promising route for high-performance functional textiles. Full article

Advancements in flexible, low-cost, and recyclable alternatives to transparent conductive oxides (TCOs) are critical challenges in the sustainability of third-generation solar cells. This work introduces a copper mesh-based transparent electrode for dye-sensitized solar cells, replacing conventional fluorine doped-tin oxide (FTO)-coated glass to simultaneously reduce spectral reflection losses, enhance mechanical flexibility, and enable material recyclability. Titanium dioxide (TiO₂) photoanodes were synthesized and directly deposited onto the mesh via a single-step, low-energy ball milling process, which eliminates TiO₂ paste preparation and high-temperature annealing while reducing fabrication time from over three hours to 30 min. Structural and surface analyses confirmed the deposition of high-purity anatase-phase TiO₂ with strong adhesion to the mesh branches, enabling improved dye loading and electron injection pathways. Optical studies revealed higher visible light absorption for the copper mesh compared to FTO in the visible range, further enhanced upon TiO₂ and Ru-based dye deposition. Electrochemical measurements showed that TiO₂/Cu mesh electrodes exhibited significantly higher photocurrent densities and faster photo response rates than bare Cu mesh, with dye-sensitized Cu mesh achieving the lowest charge transfer resistance in impedance analysis. Techno–economic and sustainability assessments revealed a decrease of 7.8% in cost and 82% in CO₂ emissions associated with the fabrication of electrodes as compared to conventional TCO electrodes. The synergy between high conductivity, transparency, mechanical durability, and a scalable, recyclable fabrication route positions this architecture as a strong candidate for next-generation dye-sensitized solar modules that are both flexible and sustainable. Full article

The calciothermic reduction slag (CRS) generated in heavy rare earth metal production, is rich in rare earth elements (REE) and highly amenable to recovery. In the present study, the CRS was treated with a H₂SO₄ roasting–water leaching method for the recovery of REEs. The feasibility of this process was confirmed by thermodynamic analysis. Key roasting and leaching factors governing the leaching efficiency of REE were identified and optimized. The maximum REE extraction efficiency reached 94.65% under the optimal conditions: roasting at 150 °C for 240 min with 15 mL of H₂SO₄, followed by water leaching at 20 °C for 60 min at a liquid–solid ratio of 15:1. Results of XRD, SEM, and EDS revealed that the REEs in the CRS were transformed into water-soluble rare earth sulfates after roasting. In the leaching process, the rare earth sulfate is efficiently extracted, whereas CaSO₄ has low solubility in water. A CaSO₄ product with a 98.10% purity was obtained with a calcium recovery of 90.79%, and the removal rate of fluorine in the CRS was 99.99%. The leaching kinetics of the REEs follow a diffusion plus interfacial transfer model with an apparent activation energy of –46.45 kJ·mol⁻¹. This study demonstrates that sulfation roasting–water leaching is a viable route for the comprehensive utilization of CRS. Full article

Currently, the growing demand for sustainable hydrogen makes the oxygen evolution reaction (OER) increasingly important. To boost the performance of electrochemical cells for water electrolysis, both cathodic and anodic sides need to be optimized. Noble metal catalysts for the OER suffer from high costs and limited availability; therefore, developing efficient, low-cost alternatives is crucial. This work investigates manganese-based materials as potential noble-metal-free catalysts. Mn antimonates, Mn chlorates, and Mn bromates were synthesized using ultrasound-assisted techniques to enhance phase composition and homogeneity. Physicochemical characterizations were performed using X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM), together with energy-dispersive X-ray spectroscopy (EDX) and surface area analyses. All samples exhibited a low surface area and inter-particle porosity within mixed crystalline phases. Among the catalysts, Mn_7.5O₁₀Br₃, synthesized via ultrasound homogenization (30 min at 59 kHz) and calcined at 250 °C, showed the highest OER activity. Drop-casted on Fluorine-Doped Tin Oxide (FTO)-coated Ti mesh, it achieved an overpotential of 153 mV at 10 mA cm⁻², with Tafel slopes of 103 mV dec⁻¹ and 160 mV dec⁻¹ at 1, 2, and 4 mA cm⁻² and 6, 8, 10, and 11 mA cm⁻², respectively. It also demonstrated good short-term stability (1 h) in acidic media, with a strong signal-to-noise ratio. Its short-term stability is comparable to that of the benchmark IrO₂, with a potential drift of 15 mV h⁻¹ and a standard deviation of 3 mV for the best-performing electrode. The presence of multiple phases suggests room for further optimization. Overall, this study provides a practical route for designing noble metal-free Mn-based OER catalysts. Full article

Perovskite solar cells (PSCs) rarely report, on a single-device platform, concurrent gains in optoelectronic efficiency and buried-interface mechanical robustness—two prerequisites for flexible and roll-to-roll (R2R) integration. We engineered a nanoplate-structured fluorine-doped tin oxide (NP-FTO) front electrode that couples light management with three-dimensional interfacial anchoring, and we quantified both photovoltaic (PV) and nanomechanical metrics on the same device stack. Relative to planar FTO, the NP-FTO PSCs achieved PCE of up to 25.65%, with simultaneous improvements in Voc (to 1.196 V), Jsc (up to 26.35 mA cm⁻²), and FF (to 82.65%). Nanoindentation revealed a ~28% increase in reduced modulus and >70% higher hardness, accompanied by a ~32% reduction in maximum indentation depth, indicating enhanced load-bearing capacity consistent with the observed FF gains. The low-temperature, solution-compatible NP-FTO interface is amenable to R2R manufacturing and flexible substrates, offering a unified route to bridge high PCE with reinforced interfacial mechanics toward integration-ready perovskite modules. Full article

Polyimide, a class of high-performance polymers, is renowned for its exceptional thermal stability, mechanical strength, and chemical resistance. However, in the context of high-integration and high-frequency electronic packaging, polyimides face critical challenges including relatively high dielectric constants, inadequate thermal conductivity, and mechanical brittleness. Recent advances have focused on molecular design and composite engineering strategies to address these limitations. This review first summarizes the intrinsic properties of polyimides, followed by a systematic discussion of chemical synthesis, surface modification approaches, molecular design principles, and composite fabrication methods. We comprehensively examine both conventional polymerization synthetic routes and emerging techniques such as microwave-assisted thermal imidization and chemical vapor deposition. Special emphasis is placed on porous structure engineering via solid-template and liquid-template methods. Three key modification strategies are highlighted: (1) surface modifications for enhanced hydrophobicity, chemical stability, and tribological properties; (2) molecular design for optimized dielectric performance and thermal stability; and (3) composite engineering for developing high-thermal-conductivity materials with improved mechanical strength and electromagnetic interference (EMI) shielding capabilities. The dielectric constant of polyimide is reduced while chemical stability and wear resistance can be enhanced through the introduction of fluorine groups. Ultra-low dielectric constant and high-temperature resistance can be achieved by employing rigid monomers and porous structures. Furthermore, the incorporation of fillers such as graphene and boron nitride can endow the composite materials with high thermal conductivity, excellent EMI shielding efficiency, and improved mechanical properties. Finally, we discuss representative applications of polyimide and composites in electronic device packaging, EMI shielding, and thermal management systems, providing insights into future development directions. Full article

With improvements in living standards, the demand for antibacterial self-cleaning coatings has significantly increased. In this work, self-cleaning coatings with antibacterial properties were fabricated by spray-coating a composite of fluorinated acrylic resin and Ag/SiO₂ nanoparticles with quaternary ammonium salts. The synergistic action of the quaternary ammonium salts and silver nanostructures caused the coating to show a dual antibacterial effect. The Ag/SiO₂ nanoparticles roughened the coating’s surface and, in combination with the fluorinated chains, provided the surface a superhydrophobic self-cleaning property with a contact angle of 156° and a sliding angle of less than 2°. Notably, the composite coating withstood 100 abrasion cycles without losing its superhydrophobicity and the contact angle is still exceeded 150° after 60 h of immersion solutions with different pH values, demonstrating outstanding wear resistance and acid/alkali stability. The incorporation of nanostructured antibacterial agents was effective in improving the roughness and antibacterial properties of the low-surface-energy resin, resulting in a self-cleaning antibacterial composite coating. This method may pave a new route for the design of functional coating materials with excellent overall performance. Full article