Search Results (1,264)

This study reports the synthesis and catalytic evaluation of a series of imidazolium-based polymeric ionic liquids (PILs) for the cycloaddition of CO₂ to epichlorohydrin (ECH). The synthesized catalysts include homopolymers, poly(3-hydroxyethyl-1-vinylimidazole chloride) (p[HVIm][Cl]) and poly(3-carboxymethyl-1-vinylimidazole chloride) (p[CMVIm][Cl]), and their block copolymers with polystyrene, synthesized for the first time, pS-b-p[HVIm][Cl] and pS-b-p[CMVIm][Cl]. Structural characterization by NMR, IR spectroscopy, and gel permeation chromatography confirmed the successful synthesis. The block copolymers exhibited a low polydispersity index (PDI 1.1–1.2), which is indicative of homogeneous chain lengths and the propensity to form ordered nanostructures, whereas the homopolymers showed higher PDI (2.4–2.9). Catalytic testing at 90 °C and 1 MPa CO₂ for 4 h revealed a clear activity trend: p[CMVIm][Cl] < p[HVIm][Cl] < pS-b-p[CMVIm][Cl] < pS-b-p[HVIm][Cl], with conversions exceeding 75% for all catalysts and a maximum of 82.69% for pS-b-p[HVIm][Cl]. These results demonstrate that the catalytic performance of PILs is governed by a synergistic interplay between the local chemical functionality of the ionic moiety and the overall polymer architecture. Based on these results, the synthesized polymeric ionic liquids, particularly pS-b-p[HVIm][Cl], demonstrate strong potential for creating multifunctional materials. Their ability to self-assemble into ordered nanostructures with distinct hydrophobic and hydrophilic domains provides a foundational architecture for combined gas separation and catalysis. The observed “micellar catalytic effect”, which enhances local reagent concentration near active sites, could be leveraged in a membrane reactor to simultaneously capture and convert CO₂ directly within the membrane. This integrated “separation–reaction” approach represents a promising strategy for advancing circular carbon economy technologies. Full article

This research aimed to quantify and investigate the morphology of microplastics in skincare and treatment creams related to their chemical composition and the potential risks to human health associated with exposure to microplastics by dermal contact. A total of 21 skincare and treatment cream samples, indicating the target audience (men, women, and children) for each product, and potential diseases were analyzed in terms of the hidden risk of microplastics. To determine the exact number of microplastics to which adults and children are exposed over the course of a year, in-depth research was conducted on the cosmetic care and treatment products used by over 354 respondents from Romania. This study used a free, self-reported questionnaire method, which took into account consumer habits and preferences, as well as any potential medical conditions that could affect exposure. Optical microscopy and micro-FTIR revealed a total of 109 microplastics, with different sizes, colors, and shapes (i.e., fragments and fibers) and various chemical compositions, including mixtures of polymeric and natural structures, as well as 100% synthetic materials, e.g., polyethylene and polyester. The potential health risk of exposure to microplastics in certain cosmetic formulations for adults was assessed by calculating various risk indices, such as the polymer risk index (H), pollution load index (PLI), dermal plastic absorption (DPA), chronic daily dermal exposure (CDDE), risk to human health from dermal absorption (RHHDA), and estimated annual dermal absorption (EADA). These indices were calculated based on the medical conditions and application areas indicated on the labels of the analyzed creams (i.e., skincare and treatment), for both adult and children’s categories, using the fingertip unit (FTU) method for estimating the cream amount. The plastic toxicity of the analyzed samples was assessed using the H and PLI indices. The risk of microplastics to human health from dermal exposure was assessed using the DPA, CDDE, RHHDA, and EADA indices, which showed concerning results regarding the presence of these particles in cosmetic formulations. Full article

Amphiphilic copolymers based on polystyrene and polyglycidol combine the chemical inertness of polystyrene with the biocompatibility of polyglycidol, making them attractive materials for polymeric micelles. While comb-like architectures have been explored to control micellization behavior and biological response, a direct comparison between comb-like and coil-comb topologies in polystyrene–polyglycidol copolymers at identical polyglycidol content remains insufficiently investigated. In this work, amphiphilic comb-like and coil-comb polystyrene–polyglycidol copolymers were synthesized via copper-catalyzed azide–alkyne click chemistry by grafting a monoalkyne-terminated polyglycidol precursor onto azide-functionalized random and block styrene copolymers. The copolymers were characterized by size exclusion chromatography and nuclear magnetic resonance. Polymeric micelles were prepared by nanoprecipitation, and their self-assembly in aqueous solution was investigated by critical micelle concentration determination, dynamic and electrophoretic light scattering, and atomic force microscopy. Both copolymers formed stable aqueous dispersions and exhibited comparable critical micelle concentrations. At identical polyglycidol content, the random copolymer formed a uniform, monomodal micellar population, whereas the block-based coil-comb architecture led to bimodal size distributions, indicating the coexistence of two distinct micellar populations. The investigated systems showed low cytotoxicity and did not induce significant oxidative stress within the studied concentration range. On isolated rat brain sub-cellular fractions (synaptosomes, mitochondria and microsomes), administered alone, the comb-like and coil-comb polystyrene-polyglycidol copolymers did not reveal statistically significant neurotoxic effects. The results demonstrate that macromolecular architecture plays a key role in governing micellar organization and in vitro biological response in polystyrene–polyglycidol copolymers, highlighting their potential as architecture-controlled polymer-based nanocarriers. Full article

Background/Objectives: The classification of adhesive systems has historically relied on the type of etching agent and the sequence of application steps, distinguishing etch-and-rinse and self-etch categories. However, these models do not encompass the versatility introduced by universal adhesives or other emerging polymeric materials. This review aimed to integrate etching technique as a defining parameter within adhesive classification, linking material composition, bonding strategy, and clinical execution into a coherent functional framework. Methods: A structured narrative review of experimental, translational, and clinical studies published between 2010 and 2025 was conducted using PubMed and Scopus. Literature addressing adhesive categories, etching strategies, etching techniques, and smear layer characteristics was critically synthesized to identify functional relationships relevant to bonding performance and clinical decision-making. Results: The proposed taxonomy classifies materials as conventional, universal, touch-cure primers, self-adhesive/universal, and glass ionomer cements. Bonding strategies are organized as etch-and-rinse, self-etch, pre-etched, and unassisted, while etching techniques are defined as selective or nonselective families encompassing five clinically defined techniques. Incorporating etching technique clarifies the role of smear layer density, the acidity of adhesive materials, and functional monomer reactivity in demineralization and bonding. This structure enhances the understanding and teaching of adhesive concepts and supports evidence-based clinical selection of materials and techniques. Conclusions: Integrating etching technique into adhesive classification provides a functional and dynamic framework that unifies material, strategy, and technique. This taxonomy facilitates clinical decision-making and can evolve with future adhesive formulations. Further independent, long-term studies are warranted to validate the proposed combinations of materials and etching procedures. Full article

The management of dental caries has evolved from the traditional mechanical approach of “extension for prevention” to a biologically oriented philosophy centered on preserving natural tooth structures. Minimally invasive dentistry (MID) emphasizes early detection, risk assessment, prevention, and conservative intervention based on the lesion’s activity and depth. This review outlines current evidence on non-operative, micro-invasive, and minimally invasive strategies, including fluoride therapy, remineralizing agents such as casein phosphopeptide–amorphous calcium phosphate (CPP-ACP), self-assembling peptides that promote biomimetic enamel repair, sealants, and resin infiltration. Minimally invasive operative methods employ advanced technologies for selective tissue removal—chemomechanical systems (Carisolv, Papacarie, Brix3000), sono-and airabrasion, and new-generation polymeric and ceramic burs (SmartBur, Cerabur) designed to preserve sound dentin. Laser photoablation, particularly with erbium lasers (Er:YAG, Er,Cr:YSGG), enables precise cavity preparation with minimal thermal and mechanical stress. These approaches enhance patient comfort, reduce anesthesia requirements, and maintain tooth vitality. Despite limitations related to cost, equipment, and operator sensitivity, MID represents not only a set of refined clinical techniques but also a comprehensive, evidence-based treatment philosophy founded on biological principles, structural preservation, and the promotion of long-term oral health. Full article

The development of smart coatings with active protection is a promising approach to prolonging the service life in extreme environments. Herein, the corrosion inhibitors 2-mercaptobenzimidazole (MBI) and CeO₂ were in situ loaded onto the surface of graphene oxide (GO) by dopamine (DA) polymerization, and we ultimately obtained the multifunctional composite MBI@CeO₂@PDA@GO (MCPG). The electrochemical impedance spectroscopy (EIS) results revealed that after 30 days of immersion in the corrosive media, the |Z|_0.01 Hz value of MCPG/WEP coating remained at 3.7 × 10⁹ Ω/cm², which displayed four orders of magnitude higher than that of pure WEP coating (1.4 × 10⁵ Ω/cm²). In a 200 h salt spray test, the MCPG/WEP coating also demonstrated minimal corrosion products and bubbles, affirming the exceptional corrosion-inhibiting effect and excellent self-healing performance. Consequently, the synergistic combination of pH-sensitive properties and outstanding barrier effect imparted dual active/passive anti-corrosion capabilities to the coating, resulting in long-lasting metal protection. Full article

Polyester/cotton blended fabrics—valued for comfort and durability—face significant fire hazards due to a synergistic “scaffold effect” during combustion. Conventional treatments with high temperature or some acidic phosphorus flame retardants during preparation often compromise the mechanical strength. Inspired by mussel adhesion chemistry, a mechanically enhanced polyester/cotton fabric was developed by using a novel bio-inspired phosphorus/nitrogen (P/N) synergistic coating. A uniform polydopamine-polyethylenimine (PDA-PEI) layer is rapidly deposited via co-deposition, suppressing dopamine self-polymerization. Subsequent covalent bonding with 2,2-dimethyl-1,3-propanediyl bis (phosphoryl chloride) (DPPC) establishes a robust P/N network. The fabricated PDA-PEI/DPPC coating reduces peak heat release rate (pHRR) and total heat release (THR) by 57.7% and 32.6%, respectively, in cone calorimetry, achieving self-extinguishment and a high limiting oxygen index (LOI) of 24.6%. Remarkably, the coating simultaneously increases the weft-direction breaking strength by 55% and elongation at break by 27.2%; these changes overcome the typical mechanical degradation associated with acidic phosphorus flame retardants. A comprehensive analysis reveals a synergistic mechanism: phosphoric acids catalyze cellulose dehydration and char layer formation in the condensed phase (90% stable C–C bonds), while radical scavengers (PO·, HPO·, and PDA) and non-flammable gases suppressed gas-phase combustion. This work presents a facile and effective strategy for fabricating high-performance and mechanically robust flame retardant polyester/cotton textiles, demonstrating the significant potential for improving fire safety in practical applications. Full article

Cellulose nanofibers/metal-organic framework (CNFs/MOF) composites hold promise for energy storage thanks to high porosity, large specific surface area, and inherent flexibility, but their poor conductivity limits applications to environmental remediation and gas adsorption. Herein, flexible CNFs served as substrates for in situ growth of continuous ZIF-8 nanolayers via interfacial synthesis, with a CNFs/ZIF-8 gel network built to enhance structural integrity and flexibility. A novel strategy first regulated the layered pore structure: ZIF-8 in CNFs/ZIF-8 nanofibers was etched in the acidic environment of aniline in situ polymerization, constructing a hierarchical porous architecture with interconnected micropores and mesopores. CNFs/ZIF-8/PANI gel composite membranes were then fabricated. As self-supporting electrodes for symmetric supercapacitors, the composites showed excellent electrochemical performance: 1350 F/g at 1 A/g for the electrode, and the flexible solid-state device delivered a specific capacitance of 220.9 F/g at 0.5 A/g, along with a capacitance retention rate of 74% after 5000 charge–discharge cycles at 10 A/g. The superior performance stems from synergistic hierarchical pore structure regulation via partial MOF sacrificial templating and gel matrix-mediated rapid ion diffusion, offering a feasible approach for high-performance flexible energy storage devices. Full article

The plasma-catalytic conversion of CO₂ is a promising route toward sustainable fuel and chemical production under mild operating conditions. However, many aspects still need to be better understood to improve performance and better understand the catalyst-plasma synergies. Among them, one aspect concerns understanding whether photons emitted by plasma discharges could induce changes in the catalyst, thereby promoting interaction between plasma species and the catalyst. This question was addressed by investigating the CO₂ splitting reaction in a planar dielectric barrier discharge (pDBD) reactor using titania-based catalysts that simultaneously act as discharge electrodes. Four systems were examined feeding pure CO₂ at different flow rates and applied voltage: bare titanium gauze, anodically formed TiO₂ nanotubes (TiNT), TiNT decorated with Ag–Au nanoparticles (TiNTAgAu), and TiNT supporting Ag–Au nanoparticles coated with polyaniline (TiNTAgAu/PANI). The TiNTAgAu exhibited the highest CO₂ conversion (35% at 10 mL min⁻¹ and 5.45 kV) and the most intense optical emission, even in the absence of external light irradiation, suggesting that the improvement is primarily attributed to plasma–nanoparticle interactions and self-induced localized surface plasmon resonance (si-LSPR) rather than conventional photocatalytic pathways. SEM analyses indicated severe plasma-induced degradation of TiNT and TiNTAgAu surfaces, leading to performance decay over time. In contrast, the TiNTAgAu/PANI catalyst retained structural integrity, with the polymeric coating mitigating plasma etching while maintaining competitive efficiency. There is thus a complex behavior with catalytic performance governed by nanostructure stability, plasmonic enhancement, and the interfacial protection. The results demonstrate how integrating plasmonic nanoparticles and conductive polymers can enable the rational design of durable and efficient plasma-photocatalysts for CO₂ valorization and other plasma-assisted catalytic processes. Full article

The synthesis of enantiomerically pure chiral β-nitroalcohols is a crucial objective in asymmetric catalysis. In order to efficiently obtain such chiral products, we developed a series of thermoresponsive, oxazoline–copper catalysts (Cu^II-PN_xFe_yO_z) via sequential reversible addition–fragmentation chain transfer (RAFT) polymerization. These catalysts can self-assemble in water into single-chain nanoparticles (SCNPs) with biomimetic behavior, in which intramolecular hydrophobic and metal-coordination interactions generate a confined hydrophobic cavity. Comprehensive characterization by FT-IR, TEM, DLS, CD, CA, and ICP analysis confirmed the nanostructure and composition. When applied to the aqueous-phase asymmetric Henry reaction between nitromethane and 4-nitrobenzaldehyde, the optimal catalyst (2.0 mol%) achieved a quantitative yield (96%) with excellent enantioselectivity (up to 99%) within 12 h. Furthermore, the thermosensitive poly(N-isopropylacrylamide, NIPAAm) block enabled facile catalyst recovery through temperature-induced precipitation above its lower critical solution temperature (LCST). This work presents an efficient and recyclable biomimetic catalytic system, offering a novel strategy for designing sustainable chiral catalysts for green organic synthesis. Full article

Self-powered perovskite photodiodes provide an attractive platform for low-power and high-sensitivity photodetection; however, their performance capabilities are often constrained by inefficient interfacial charge extraction and noise suppression. Here, we report a polymer-mediated interfacial engineering strategy for methylammonium lead iodide (MAPbI₃) photodiodes by integrating thermally optimized nickel oxide (NiO_x) hole-transport layers (HTLs) with a nonionic polymeric surfactant, poly(oxyethylene)(10) tridecyl ether (PTE). NiO_x films annealed at 300 °C establish a favorable energetic baseline for hole extraction, while the ppm-level incorporation of PTE into the MAPbI₃ precursor enables the molecular-scale modulation of the NiO_x/MAPbI₃ interface without forming an additional interlayer. The external quantum efficiency at 640 nm increases from 78.7% for pristine MAPbI₃ to 84.1% and 84.6% for devices incorporating 30 and 60 ppm PTE, corresponding to enhanced responsivities of 406, 434, and 437 mA/W. These improvements translate into reduced noise-equivalent power and an increase in the noise-limited detectivity from 2.50 × 10¹² to 2.76 × 10¹² Jones under zero-bias operation. Importantly, enhanced sensitivity is achieved without compromising the dynamic performance, as all devices retain fast temporal responses and kilohertz-level bandwidths. These results establish polymeric-surfactant-assisted interfacial engineering as a scalable and effective platform for low-noise, high-sensitivity self-powered perovskite photodiodes for renewable-energy-integrated systems. Full article

The recent development in polymer science has gone beyond the traditional linear and randomly functionalizable macromolecules to the architected polymer systems, which integrate modular synthesis and dynamic responsiveness. Although the literature related to polymer synthesis and stimuli-responsive materials and applications is widely discussed, it is common to review the aspects independently, restricting a complete picture of how architectural modularity controls adaptive performance. This gap is filled in this review with an integrated framework of relating modular polymer synthesis, stimuli-responsive design, and application-oriented functionality in a single coherent design philosophy. The scientific novelty of this review is that the focus on modular polymers is not only on synthetic constructs, but is a programmable functional scaffold where the structural precision is the direct determinant of responsiveness, multifunctionality, and performance. Controlled polymerization and post-polymerization modification regimes are mentioned to be tools that allow precise positioning of functional modules, and this allows polymers to respond in predictable ways to environmental stimuli like pH, temperature, light, redox conditions, etc. In addition, the review identifies the role of a synergistic combination of various responsive modules in the emergence of behaviours that would not be reached in conventional polymer systems. This review offers a coherent viewpoint on the future of functional polymers of the next generation by bringing together synthetic approaches to nano-responsive behaviour and real-world technologies, such as drug delivery, self-healing surfaces, adaptive surfaces, and biosensing surfaces. The framework in the present paper provides a logical route towards the development of environmentally friendly, multifunctional, and adjustable polymer structures. Full article

Conductive hydrogels that simultaneously exhibit high mechanical robustness, reliable electrical conductivity, and interfacial adhesion are highly desirable for flexible sensing applications; however, achieving these properties in a single system remains challenging due to intrinsic structure–property trade-offs. Herein, a multifunctional conductive hydrogel (ASP hydrogel) is developed based on a polyacrylamide (PAM)/sodium alginate (SA) double-network architecture using a gallic acid (GA)–Fe³⁺–pyrrole (Py) coupling strategy. In this design, GA provides metal-coordination sites for Fe³⁺, while Fe³⁺ simultaneously serves as an oxidant to trigger the in situ polymerization of pyrrole, enabling the homogeneous integration of polypyrrole (PPy) conductive networks within the hydrogel matrix. The resulting ASP hydrogel exhibits a markedly enhanced fracture strength of 2.95 MPa compared with PAM (0.26 MPa) and PAM–SA (0.22 MPa) hydrogels, together with stable electrical conductivity and reproducible strain-dependent electrical responses. Moreover, the introduction of dynamic metal–phenolic coordination and hydrogen-bonding interactions endows the hydrogel with intrinsic self-healing capability and strong adhesion to diverse substrates. Rather than relying on simple filler incorporation, this work demonstrates an integrated network design that balances mechanical strength, conductivity, and adhesion, providing a versatile material platform for flexible strain sensors and wearable electronics. Full article

Enhancing the flame retardancy of polymeric materials by adding only eco-friendly ammonium polyphosphate (APP) while simultaneously maintaining high-temperature resistance has become a challenge. Talcum has been introduced as a cooperative agent into the silicone rubber/APP system to investigate the effect of talcum on flame retardancy, thermal stability, and high-temperature resistance. The machining process induces the orientation of talcum in the system. The ceramifiable silicone rubber blends containing oriented talcum (e.g., sample SA₆T₄) exhibited superb flame retardancy, including an LOI of 29.4%, a UL-94 rating of V-0, and a peak heat release rate (PHRR) of 250.2 kW·m⁻². More importantly, the blends present excellent thermal stability and high-temperature resistance, characterized by outstanding self-supporting properties and dimensional stability. Based on the structural analysis of the blends and their residues, the made of action for the improved flame retardancy may be attributed to the formation of a compact barrier layer. This layer is formed by oriented talcum platelets combined with phosphoric acid, from the thermal decomposition of APP, promoting crosslinking, thereby achieving a good inhibition barrier to inhibit heat feedback from the condensation zone. The excellent thermal stability and high-temperature resistance of the ceramifiable silicone rubber blends may be ascribed to a cooperative effect between APP and talcum at high temperatures, which facilitates the formation of ceramic structures. The novel ceramifiable silicone rubber composite has potential applications as flame-retardant sealing components for rail transit equipment and encapsulation materials for new energy battery modules. Full article

This review provides a comprehensive overview of recent progress in chitin-based nanomaterials and their composite engineering. Particular focus is placed on techniques for constructing self-assembled chitin nanofibers (ChNFs) with tightly bundled fibrillar structures, as well as strategies for fabricating composites in which the ChNFs serve as reinforcing components, combined with natural polymeric matrices. In addition, high-crystalline scaled-down (SD-)ChNFs were fabricated through partial deacetylation of the ChNFs, followed by electrostatic repulsive disassembly of the abovementioned bundled fibrils in aqueous acetic acid, which were further used to reinforce composites comprising the other polysaccharides. Mixing the SD-ChNFs with low-crystalline chitin substrates further enabled the fabrication of all-chitin composites (AChCs) that exploit crystallinity contrast to achieve enhanced tensile strength. Moreover, the AChC films exhibited high cell-adhesive properties and promoted the formation of three-dimensional cell-networks, highlighting their potential for biomedical applications. Full article