Search Results (1,509)

CO₂ laser processing has emerged as an efficient dry-finishing technique capable of inducing controlled chemical and morphological transformations in cotton and denim textiles. The strong mid-infrared absorption of cellulose enables localised photothermal heating, leading to selective dye decomposition, surface oxidation, and micro-scale ablation while largely preserving the bulk fabric structure. These laser-driven mechanisms modify colour, surface chemistry, and topography in a predictable, parameter-dependent manner. Low-fluence conditions predominantly produce uniform fading through fragmentation and oxidation of indigo dye; in comparison, moderate thermal loads promote the formation of carbonyl and carboxyl groups that increase surface energy and enhance wettability. Higher fluence regimes generate micro-textured regions with increased roughness and anchoring capacity, enabling improved adhesion of dyes, coatings, and nanoparticles. Compared with conventional wet processes, CO₂ laser treatment eliminates chemical effluents, strongly reduces water consumption and supports digitally controlled, Industry 4.0-compatible manufacturing workflows. Despite its advantages, challenges remain in standardising processing parameters, quantifying oxidation depth, modelling thermal behaviour, and assessing the long-term stability of functionalised surfaces under real usage conditions. In this review, we consolidate current knowledge on the mechanistic pathways, processing windows, and functional potential of CO₂ laser-modified cotton substrates. By integrating findings from recent studies and identifying critical research gaps, the review supports the development of predictable, scalable, and sustainable laser-based cotton textile processing technologies. Full article

In this work, sodium alginate/chitosan (SA/CS) blend films were prepared by thermo-compression for the first time. Glycerol and lactic acid were used as de-structuring agents for SA and CS, respectively. The chemical structures, thermal stability, phase morphology, mechanical properties, water resistance, film opacity, film color, and soil burial test of thermo-compressed SA/CS films were investigated. The results indicate that intermolecular interactions in polyelectrolyte complexes in SA/CS blends were detected. Blending with CS improved the thermal stability of SA-based films. The SA/CS films showed excellent phase compatibility between SA and CS. The addition of CS improved the tensile properties of the SA-based films. The incorporation of CS in SA films resulted in enhanced water resistance and opacity and a decrease in biodegradability under soil burial. Thermo-compressed SA/CS films show promise for development and increased production capacity. These films can be tailored by varying the SA/CS ratios to display different properties. This versatility makes them suitable for a range of sustainable and diverse applications, including wound dressing, drug delivery, biosorbents, and packaging. Full article

The escalating global water crisis demands the development of cost-effective and environmentally sustainable treatment technologies. Among various advanced oxidation processes (AOPs), peracetic acid (PAA) has emerged as a promising oxidant, owing to its high redox potential, chemical stability, and potent disinfection capability. Nevertheless, the lack of highly efficient catalysts remains a major obstacle to achieving the effective degradation of contaminants of emerging concern in wastewater. Heterogeneous catalysis has proven to be a viable strategy for enhancing PAA activation, highlighting the urgent need for catalysts with superior activity, stability, and recyclability. Metal–organic frameworks (MOFs), with their large surface areas, tunable porosity, and structural diversity, provide versatile platforms for catalyst design. Recently, MOF-derived materials have attracted increasing attention for PAA activation, offering a new frontier in advanced oxidation technologies for efficient and sustainable wastewater remediation. This review systematically examines the role of MOFs in PAA activation, from pristine frameworks to MOF-based composites and MOF-derived catalysts. Mechanistic insights into PAA activation are highlighted, strategies for engineering MOF-based composites with synergistic catalytic properties are discussed, and the transformation of MOFs into robust derivatives with improved stability and reactivity is explored. Special attention is given to the identification and quantification of reactive species generated in PAA systems, providing a critical understanding of reaction pathways and catalytic performance. Finally, current challenges and future directions are outlined for designing highly efficient, recyclable, and environmentally compatible MOF-based catalysts, emphasizing their potential to significantly advance PAA-based AOPs. Full article

The objective of this research is to develop environmentally friendly, risk-free and effective adsorbent composite beads that remove Cu(II) ions from aqueous solutions using cost-effective biopolymers (Carboxymethylcellulose (CMC) and sodium alginate (AL)). The synthesized hydrogel beads (AL@CMC) were dried using two drying modes, namely air-drying and freeze-drying, and characterized using scanning electron microscopy (SEM), Fourier Transform Infrared Spectroscopy (FT-IR), and Brunauer–Emmett–Teller (BET) analysis. The study investigated factors such as pH, adsorbent dosage, reaction time, Cu(II) ions concentration, and temperature to elucidate the adsorption mechanisms involved in removing copper ions. The results indicated that the hydrogel exhibited a maximum adsorption capacity of 99.05 mg·g⁻¹, which is highly competitive compared to previous studies; the AL@CMC beads prepared in this work show a significantly higher adsorption capacity, improved stability due to the interpenetrated biopolymer network, and a clear enhancement from freeze-drying, which greatly increases porosity and active surface area. In addition, the pseudo-second-order nonlinear kinetic model best described the experimental data, implying the chemical nature of the adsorption process. Furthermore, the thermodynamic studies revealed that the adsorption process was endothermic, spontaneous, and homogenous. A Monte Carlo simulation model was utilized to ensure compatibility with the adsorption mechanism, in order to delve deeper into the intricacies of the adsorption process and gain a more comprehensive understanding of its underlying mechanisms and behavior. In conclusion, the prepared hydrogel beads proved to be an effective adsorbent for efficiently removing copper ions, making them a promising solution for addressing Cu(II) ion pollution. Full article

Berry crops such as strawberry Fragaria × ananassa (Weston), raspberry Rubus idaeus L., blackberry Rubus ulmifolius Schott, 1818, and blueberry Vaccinium myrtillus L. are economically and nutritionally valuable worldwide. However, the intensive use of synthetic pesticides for pest management in these crops has led to ecological imbalance, pest resistance, and negative effects on non-target organisms and human health. The integration of biological control agents into sustainable integrated pest management (IPM) systems represents an alternative. This review compiles and evaluates current advances in the application of baculoviruses (BVs), entomopathogenic fungi (EPFs), nematodes (EPNs), predatory mites (PMs), and parasitoid wasps (PWs) for pest suppression in berry crops. Emphasis was placed on their ecological interactions, host specificity, and compatibility within IPM frameworks. The combined use of micro- and macrobiological control agents effectively reduces key pest populations. However, field efficacy remains influenced by abiotic stressors such as UV radiation, temperature fluctuations, and chemical incompatibility. The integration of native micro- and macrobiological control agents of through conservation biological control (CBC) strategies can enhance sustainability in berry production systems. Future efforts should focus on formulation improvements, adaptive management under field conditions, and synergistic interactions among microbial and arthropod natural enemies. Full article

The advancement of efficient and stable perovskite solar cells (PSCs) increasingly depends on developing flexible, metal-free electrode architectures. Single-walled carbon nanotubes (SWCNTs) offer chemical robustness, high conductivity, and mechanical flexibility, making them promising candidates to replace brittle metal cathodes. However, pristine SWCNTs are intrinsically p-type, creating energy barriers and recombination losses in inverted (p–i–n) PSCs. Achieving stable n-type doping compatible with both SWCNTs and perovskites is therefore critical. Here, seven representative n-type dopants, small molecules (TBD and TPP), ionic salts (TBAI, TBABr, and B18C6·KCl), and polymers (PEI and PVP) were systematically investigated to elucidate their effects on doping efficiency and interfacial stability. Morphological, structural, and electronic analyses supported by DFT calculations reveal that strong bases and ionic dopants promote perovskite degradation, whereas polymeric and coordination-type dopants preserve crystallinity and surface uniformity. Among them, PEI- and TPP-doped SWCNT electrodes achieved the best device performance, with power conversion efficiencies of 9.6% and 8.1%, respectively, demonstrating efficient electron extraction and interfacial stability. These findings highlight that interfacial chemical compatibility rather than intrinsic donor strength governs the effectiveness of n-type SWCNT doping, providing rational design principles for stable, metal-free perovskite photovoltaics. Full article

The increasing number of waste rubber tires has attracted the attention of more and more researchers. Rubber asphalt has better performance compared with original asphalt. However, the compatibility between rubber powder and asphalt is poor because of the difference in physical and chemical properties and the improvement of high-temperature performance of asphalt by rubber powder is very limited. The compatibility between rubber powder and original asphalt plays a key role in the storage stability and rheological performance of rubber asphalt. This paper provides a comprehensive overview of rubber asphalt, factors influencing compatibility, compatibility evaluation methods, and improvement approaches. Desired compatibility results from the fact that rubber powder is cross-linked with molecules of original asphalt and evenly distributed in the original asphalt, forming a homogeneous system. Starting from the preparation process of rubber asphalt, the best preparation process was summarized. Then the activity of rubber powder is improved by physical and chemical methods, or other additives are added to finally promote the formation of a cross-linking network structure between rubber powder and original asphalt. Rheological method is the most widely used method in compatibility evaluation, but it is gradually accepted by researchers to evaluate the compatibility by observing the molecular morphology of rubber asphalt. Full article

Background: Lewisite, a potent chemical warfare agent, induces rapid and progressive cutaneous damage, necessitating treatment strategies that offer both immediate decontamination and prolonged therapeutic action. This study aimed to develop and evaluate a composite topical formulation comprising 4-phenylbutyric acid (4-PBA)-loaded emulsomes embedded within a foam vehicle to address both aspects of vesicant-induced skin injury intervention. Methods: Emulsomes composed of a stearic acid–cholesterol solid lipid core stabilized by a lecithin shell were prepared via thin film hydration and optimized by varying lipid ratios and drug loading parameters. Formulations were characterized for drug loading, particle size, and zeta potential. Physicochemical compatibility was assessed using Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) analyses. Stability was evaluated under accelerated refrigerated (25 °C/60% RH) and room temperature (40 °C/75% RH) conditions. The optimized formulation was incorporated into a foam base and evaluated for decontamination efficiency, drug release kinetics, in vitro permeation, and in vivo efficacy. Results: The selected formulation (E2) exhibited high drug loading (17.01 ± 0.00%), monodisperse particle size (PDI = 0.3 ± 0.07), and stable zeta potential (−40 ± 1.24 mV). FTIR and DSC confirmed successful encapsulation with amorphous drug dispersion. The emulsome-foam demonstrated dual functionality: enhanced decontamination (66.84 ± 1.27%) and sustained release (~30% over 24 h), fitting a Korsmeyer–Peppas model. In vitro permeation showed significantly lower 4-PBA delivery from E2 versus free drug, confirming sustained release, while in vivo studies demonstrated therapeutic efficacy. Conclusions: This emulsome-foam system offers a promising platform for topical treatment of vesicant-induced skin injury by enabling both immediate detoxification and prolonged anti-inflammatory drug delivery. Full article

The global phase-out of sulfur hexafluoride (SF6), an insulating gas with high global warming potential (GWP), has driven the search for eco-friendly alternatives in high-voltage equipment. Perfluoroisobutyronitrile (C4F7N) emerges as a promising candidate due to its low GWP and high dielectric strength. However, its chemical stability under circuit breaker conditions, especially when interacting with vaporized contact materials such as silver, remains a key concern. This study investigates the decomposition mechanisms of C4F7N in the presence of silver vapor using quantum chemical calculations at the B3LYP/LanL2DZ level. A reaction network comprising 35 pathways and 12 transition states were identified. All structures were confirmed as valid stationary points via frequency analysis and intrinsic reaction coordinate (IRC) calculations. Three primary reaction pathways between C4F7N and Ag were delineated, leading to secondary reactions that generate low-weight molecules and Ag-containing species such as AgF and AgCN. Key energy barriers and temperature-dependent equilibrium constants (K_eq) were determined to evaluate pathway feasibility. This work provides fundamental insights into the high-temperature interfacial chemistry of C4F7N with Ag, offering essential data for assessing its material compatibility and long-term reliability as a sustainable insulation medium in power systems. Full article

This computational study investigates the optical properties of a sixth-order Fibonacci quasi-periodic photonic crystal cavity designed for the infiltration of near-infrared colloidal quantum dots (QDs, e.g., InAs/ZnSe or PbS) and fully compatible with plasma-enhanced chemical vapor deposition (PECVD) using porous silicon layers. Using the transfer matrix method (TMM), we simulate transmission (T), reflection, absorption, electric field distributions and Purcell factors (F) for both TE and TM polarizations, incorporating the wavelength-dependent absorption of porous silicon. A multi-objective figure-of-merit is defined to simultaneously maximize transmission ($T>95\%$ at 800 nm) and the one-dimensional Purcell factor. The optimized structure ($P_H=0416$) yields a quality factor $Q\approx 4300$, a 1D Purcell factor $F_{1D}\approx 3.6$ and a realistic 3D Purcell enhancement estimated between 4 and 8 (under lateral confinement assumptions). This conservative estimate, derived via the effective index method to account for 3D effects, aligns with the detailed discussion within the article and is lower than the ideal upper bound of the 1D model. The integrated emission enhancement is approximately 3.0-fold. Monte Carlo simulations demonstrate remarkable robustness to fabrication tolerances ($\pm 10$ nm thickness variations result in a <5% reduction in transmission), highlighting the structure’s scalability for PECVD-based processing. Comparison with periodic Bragg structures reveals superior angular stability and disorder tolerance in the Fibonacci design, positioning it as a promising platform for robust QD-based light sources and integrated refractive index sensors. Full article

Natural fibers are increasingly used as sustainable, lightweight, and low-cost alternatives to glass fibers in polymer composites. However, their inherent hydrophilicity and surface polarity limit compatibility with non-polar polymer matrices. Both gas/solid and plasma fluorination modify only the surface of lignocellulosic materials. Mild conditions are mild, with reactivity governed by fluorine concentration, temperature, and material composition. Surface energy is typically assessed through contact-angle measurements and surface analytical techniques that quantify changes in hydrophobicity and chemical functionalities. In wood, fluorination proceeds preferentially in lignin-rich regions, making lignin a key component controlling reactivity and the spatial distribution of fluorinated groups. Natural fibers follow the same logic as for flax, which is a representative example of lignin content. Applications of fluorinated bio-based materials include improved moisture resistance, enhanced compatibility in composites, and functional surfaces with tailored wetting properties. Scalability depends on safety, cost, and process control, especially for direct fluorination. Durability of the treatment varies with depth of modification, and environmental considerations include the potential release of fluorinated species during use or disposal. Full article

Catalytic transfer hydrogenation (CTH) provides a practical and sustainable approach for reducing unsaturated compounds, serving as an alternative to high-pressure H₂ in laboratory and fine chemical contexts. This broad reaction class includes asymmetric transfer hydrogenation (ATH), a key strategy in enantioselective synthesis due to its operational simplicity, high stereocontrol, and compatibility with sensitive functional groups. A central variable governing CTH efficiency is the role of bases, which may function as essential activators, co-hydrogen donors, or be entirely absent depending on the catalytic system. This review provides a comparison of base-assisted, base-free, and base-as-co-hydrogen-donor CTH methodologies across diverse metal catalysts and substrates. We highlight how bases such as triethylamine, K₂CO₃, and NaOH facilitate catalyst activation, modulate hydride formation, and tune reactivity and selectivity. The dual function of bases in formic-acid-driven systems is examined alongside synergistic effects observed with mixed-base additives. In contrast, base-free CTH platforms demonstrate how tailored ligand frameworks, metal-ligand cooperativity, and engineered surface basicity can eliminate the need for external additives while maintaining high activity. Through mechanistic analysis and cross-system comparison, this review identifies the key structural, electronic, and environmental factors that differentiate base-assisted from base-free pathways. Emerging trends—including greener hydrogen donors, advanced catalyst architectures, and additive-minimized protocols—are discussed to guide future development of sustainable CTH processes. Full article

The rapid growth of the hydrogen industry, driven by global decarbonization efforts, has intensified the need for safe and large-capacity storage systems. Although hydrogen is one of the most abundant elements on Earth, its storage remains technically challenging due to its chemical reactivity and stringent containment requirements. Previous research has primarily emphasized the material-level behavior of polymer liners, composites, and metal alloys because chemical compatibility plays a critical role in aboveground high-pressure tanks. However, for underground storage systems, long-term structural stability is governed not only by material performance but also by the geo-mechanical behavior of deep rock masses. This study proposes a seismic design approach for Lined Rock Caverns (LRCs), a deep underground storage concept capable of sustaining high internal pressure. The method incorporates ground-induced deformation and evaluates the additional influence of internal pressure on lining behavior. Numerical analyses demonstrate that internal pressure has a significant stabilizing effect on the structural response by reducing ovalization and suppressing nonlinear deformation mechanisms. The results highlight that internal pressure is not a secondary load but a key design parameter that must be integrated into the seismic evaluation of LRC-based hydrogen storage facilities. Full article

To address the challenges of rutting and performance balance in asphalt pavements under high-temperature and heavy-load conditions, a novel polyolefin composite modifier (PCM-H) was developed from waste tire rubber powder, recycled ethylene vinyl acetate (EVA), acrylonitrile butadiene styrene (ABS), petroleum resin, and polymer additives. The chemical characteristics, thermal stability, and compatibility mechanisms of PCM-H were compared with those of two commercial modifiers (PCM-1 and PCM-2) using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). PCM-H exhibited superior compatibility and thermal stability. In contrast, PCM-2 tends to crystallize and precipitate within the 180–200 °C range, which is detrimental to the stability of the composite system. At an optimal dosage of 10 wt% in styrene–butadiene–styrene (SBS) modified asphalt, PCM-H formed a uniform dispersion and, through crosslinking reactions, established a three-dimensional network structure. Subsequently, the performance of composite modified asphalts, prepared with each of the three modifiers at their respective optimal dosages, was evaluated comparatively. Performance evaluations demonstrated that all polyolefin-modified asphalts significantly outperformed the conventional SBS modified asphalt. The PCM-H modified asphalt (PCM-H MA) exhibited the most superior performance, achieving a performance grade (PG) exceeding 94 °C, along with exceptional high-temperature elasticity and creep resistance, superior low-temperature cracking resistance, and enhanced fatigue healing capability. The results indicated that the crosslinked network structure effectively enhances asphalt cohesion, thereby providing a synergistic improvement in both high- and low-temperature performance. This study provides an effective solution and theoretical basis for developing high-performance pavement materials resistant to high temperatures and heavy loads conditions. Full article

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has become one of the most influential materials in neural engineering, offering high electrical conductivity, mechanical softness, and stable processing in complex aqueous media. Beyond these well-known merits, recent studies indicate that PEDOT:PSS can be regarded as a bio-solid electrolyte interphase (bio-SEI) that governs the interactions between neural probes and biological tissue. In this framework, PEDOT:PSS functions as a selective and adaptive interphase that mediates ion and electron transport, buffers mechanical mismatch, and mitigates chemical or biological degradation at the device-tissue boundary. This review critically summarizes the progress in molecular design, synthesis, and post-treatment strategies that enhance PEDOT:PSS stability and compatibility within physiological environments. Developments such as polydopamine-assisted adhesion, zwitterionic modification, and hybridization with soft hydrogels have expanded its role from a passive coating to an active, self-regulating interphase that prolongs implant performance. We further discuss how the hierarchical structure of PEDOT:PSS—from its molecular organization to device-level morphology—contributes to long-term electrochemical and biological stability. By treating PEDOT:PSS as an intrinsic bio-SEI rather than a simple conductive coating, this perspective highlights its central role in the development of durable, biocompatible, and intelligent neural interfaces for next-generation implantable electronics. Full article