Search Results (338)

As cutting-edge semiconductor devices become smaller and more densely packed (i.e., ultra large-scale integration, ULSI), there is an increased risk of parasitic capacitance preventing proper device operation. There is consequently growing interest in the development of low-permittivity dielectric materials to serve as intermetal/interlayer coatings that would minimize this effect. Highly porous aerogels exhibit extremely low dielectric permittivity; silica-based aerogel films, in particular, are candidates for this application. The present report focuses on the synthesis, structure and dielectric permittivity of hydrophobic, tetramethyl orthosilicate (TMOS)-based silica aerogels prepared in disc-form. Using our 3D printed polymer sample holder with few metallic components, we are now able to determine the dielectric permittivity of highly porous, hydrophobic silica aerogels in the very low frequency (VLF) range, 10–27 kHz. Commercial systems that operate in the VLF range include circuits for biological signal processing, characterized by low amplitude and frequency, and circuits that operate in marine environments, where the useful frequency range is limited by acoustic signal deterioration. During impedance measurements, aerogel samples were confined in pure, dry oxygen atmosphere. Low mass density (10–250 mg/cm³) TMOS-based aerogel discs present structural characteristics and relative dielectric permittivity values in the VLF range that are not readily comparable with analogous data reported to date in the relevant literature. Full article

Coatings based on polyvinylidene fluoride (PVDF) and poly(dimethylsiloxane) (PDMS)-based polymeric microspheres can be easily fabricated via non-solvent-induced phase separation (NIPS) and electrostatic spraying (ES) techniques. Both techniques are promising strategies for constructing superhydrophobic surfaces on various substrates. However, PVDF and PDMS inherently suffer from severe aggregation, which generates oversized particles and inhomogeneous microstructures. Conventionally, costly and environmentally hazardous dispersants are required to alleviate this issue, severely restricting the industrial scalability and practical application of such coatings. In this work, methyltrimethoxysilane-modified cellulose nanocrystals (Si-CNCs) were introduced as a green multifunctional modifier to tackle these issues. The results revealed that as structural building blocks and dispersants, Si-CNCs inhibited polymer aggregation via electrostatic repulsion and steric hindrance, refined the particle size and formed uniform micro/nano hierarchical structures. Increasing Si-CNC loading further improved polymer dispersion and superhydrophobic performance. Coatings fabricated by ES showed better hydrophobicity than those fabricated by NIPS. ES achieved a water contact angle (WCA) of 160–166° and a sliding angle (SA) near 1° on cotton fabric, while NIPS had a WCA of 153.8–158° and an SA of around 2°. Wood and glass substrates also obtained favorable superhydrophobicity, with WCAs above 150° and SAs below 1°. Furthermore, all modified surfaces exhibited excellent abrasion resistance. This work provides a relatively eco-friendly, environmentally sustainable, scalable and substrate-flexible strategy for fabricating high-performance PVDF/PDMS-based superhydrophobic coatings. Full article

Background/Objectives: Polymethyl methacrylate (PMMA) is widely used in medical and dental applications because of its favorable mechanical properties and ease of processing. However, its clinical performance is limited by low surface hardness, hydrophobicity, and susceptibility to microbial colonization and biofilm formation. This study aimed to investigate the effects of amorphous titanium dioxide (TiO₂) nanolayers deposited by atomic layer deposition (ALD) on the surface morphology and antibacterial properties of PMMA-based materials. Methods: Amorphous TiO₂ coatings were deposited on bone cement PMMA and dental PMMA substrates using ALD with TiCl₄ and H₂O precursors at 80 °C. The low deposition temperature enabled the conformal of thermally sensitive polymer substrates. Surface characterization was performed using atomic force microscopy (AFM) and scanning electron microscopy (SEM) to evaluate coating morphology and nanoscale topography. Antibacterial activity was assessed against S. aureus and P. aeruginosa through planktonic growth and biofilm formation assays, with additional evaluation of ultraviolet (UV) activation and surface polishing. Results: AFM analysis revealed that amorphous TiO₂ coating on standardly laboratory practice-polished PMMA increased the arithmetical mean roughness (Ra) from 1.82 nm to 14.60 nm, and maximum height (Rmax) from 36.20 nm to 298.00 nm. Polishing before coating significantly increased surface roughness and height variation, resulting in complex micro- and nanotopography. Microbiological analyses demonstrated variable antibacterial effects depending on bacterial species and surface characteristics. Comparison of planktonic growth, biofilm formation and OD590 ratio showed that amorphous TiO2 coating on polished PMMA reduced biofilm formation and planktonic growth in P. aeruginosa with a decreased OD ratio, while S. aureus biofilm formation was reduced. S. aureus had a consistently higher OD590 than P. aeruginosa. UV treatment alone did not produce consistent antibacterial enhancement. Conclusions: The study findings suggest that the surface topography had a greater role than UV treatment in determining bacterial adhesion. Surface roughness was strongly associated with S. aureus adhesion., whereas P. aeruginosa showed minimal response to the tested surface modifications. These findings suggest that TiO₂ coating after standard polishing alone may not provide consistent antibacterial activity under the tested conditions and point to the importance of nanoscale surface design in developing antimicrobial polymer biomaterials. Full article

Femtosecond laser surface texturing offers a promising route to tailor the functionality of bio-based wood coatings, yet the interplay between coating composition and laser processing remains poorly understood. In this study, bio-based epoxy coatings with eventual micronized wax additives were textured using a femtosecond laser to investigate the effects of laser processing parameters on pattern formation and resulting hydrophobicity. The epoxy coatings containing PE, PE/PTFE, HDPE, and rice bran waxes at 1, 5, and 7 wt.-% were characterized in terms of morphology, roughness, wettability, and chemical stability, followed by systematic variation of pulse repetition rate and laser power. The results reveal that the ablation threshold strongly depends on intrinsic coating properties. Ablation resistance increases with surface roughness and wax melting enthalpy, reflecting the role of phase transition energy in laser–matter interaction. The wax-filled coatings exhibit a transition from melting-dominated behavior at low energy input to ablation-dominated behavior at a higher energy. Laser texturing enhances hydrophobicity in parallel with theoretical values calculated from the Cassie–Baxter wetting model, with the highest hydrophobicity achieved for coatings combining intrinsic hydrophobicity and stable pattern formation. Chemical analysis confirms limited degradation of the epoxy matrix without significant carbonization, while wax additives provide partial thermal shielding. Overall, this work demonstrates clear options for tailoring surface morphology and wettability of hydrophobic polymer coatings through controlled femtosecond laser processing. Full article

Wood’s inherent flammability, arising from its cellular organic composition, demands effective protective strategies. This study aimed to develop a multifunctional bio-based wood coating simultaneously integrating flame retardancy, optical transparency, moisture-triggered self-healing, and surface hydrophobicity within a single formulation. An intumescent flame retardant (PAGHR) was synthesized via ionic assembly of a phytic acid–phosphorylated polyethylene glycol conjugate (PgP) with a piperazine–etidronic acid salt (HEPHR), subsequently blended with gelatin (G) and surface-finished with fluorosilane. The optimized coating (G/PAGHR-4) achieved a limiting oxygen index (LOI) of 37.2% and passed the UL-94 V-0 rating. Cone calorimetry demonstrated reductions of 75.1% in peak heat release rate (pHRR) and 50.0% in total heat release (THR) relative to the neat gelatin control. Char yield at 700 °C increased substantially from 17.8 wt% to 41.0 wt%, confirming effective condensed-phase char promotion. Beyond fire performance, the coating maintained high visible-light transmittance, preserved natural wood aesthetics, and achieved macroscopic scratch healing within 40 min upon ambient water contact. Fluorosilane finishing elevated the water contact angle to 122°. These results establish a scalable, environmentally friendly strategy for multifunctional bio-based protective coatings applicable to wood, textiles, and polymer substrates. Full article

Raw lacquer, a natural polymer derived from the bast of lacquer trees (Toxicodendron vernicifluum), is renowned as the “King of Coatings” due to its exceptional film-forming properties, abrasion resistance, corrosion resistance, and biocompatibility. However, its inherent limitations—including stringent drying conditions, slow curing rates, deep coloration, and difficult application—have severely restricted its modernization and widespread adoption. This review systematically summarizes recent research advances in the modification and application of raw lacquer, focusing on four major modification strategies: (1) Nanocomposite modification—incorporating functional nanofillers such as Al₂O₃, cellulose nanofibrils (CNF), polydopamine (PDA) melanin-like nanoparticles, and SiO₂ to significantly enhance film hardness, compactness, UV-aging resistance, and drying kinetics. (2) Chemical structure modification—employing molecular design strategies including aminoanthraquinone grafting, tung oil blending, water-based emulsification, and terpene/allyl group functionalization to improve hydrophobicity, flexibility, fast-drying properties, and achieve dual photo/oxygen curing. (3) Biomass synergistic composites—utilizing natural polymers such as chitosan and lignin, along with bio-inspired adhesion mechanisms (e.g., PDA), to confer advanced functionalities including antibacterial and antifouling properties. (4) Curing behavior regulation—precisely controlling drying kinetics through inorganic salt ion microenvironment engineering, nonionic surfactants, and salicylaldehyde Schiff base-based driers. Building upon these foundations, this review further expands on the emerging high-value applications of modified lacquer in preventive conservation of cultural heritage, advanced functional coatings (anti-corrosion, super-hydrophobicity, flame retardancy), biomedical materials (hemostasis, antibacterial activity, drug-controlled release, water treatment adsorption), and intelligent responsive flexible electronics. Finally, addressing challenges including weak fundamental research, bottlenecks in green industrialization, and lack of standardization, future development directions are proposed encompassing interdisciplinary innovation, sustainable modification strategies, integration of multifunctional intelligent systems, and big data-driven research paradigms, aiming to provide theoretical guidance and technical references for the high-value utilization and modernization of lacquer resources. Full article

We report di- and triblock copolymers that combine hydrophilic polyethers—poly(ethylene glycol) monomethyl ether (mPEG) and polyglycidol (PGl)—with a hydrophobic, degradable polyester, poly(β-butyrolactone) (P(β-BL)). A mild hydrolysis method was developed to selectively remove acetal protecting groups from poly(ethoxy ethyl glycidyl ether) (PEEGE) without cleaving the β-butyrolactone polyester backbone, enabling the preparation of PGl-b-P(β-BL) and mPEG-b-PGl-b-P(β-BL) block copolymers. Thermal analysis revealed that the glass transition temperatures (T_g) of the copolymers could be tuned by varying block composition and length. Diblock copolymers containing the PGl segment were amorphous, with T_g values ranging from −2.7 to −19.9 °C. The presence of an mPEG segment in the triblock copolymers resulted in a further decrease in T_g, reaching values between −32.3 and −38.9 °C. Solubility and water affinity studies demonstrated that incorporation of hydrophilic polyether blocks enhances copolymer–solvent interactions, leading to increased wettability of the polymer-coated surface. The water contact angle for films formed from PGl-b-P(β-BL) decreased to 53 °C, while for mPEG-b-PGl-b-P(β-BL) copolymers, it was further reduced to 43 °C compared with the hydrophobic P(β-BL) film. Hydrolytic degradation experiments showed accelerated cleavage of the P(β-BL) segment in copolymers containing hydrophilic blocks compared to the P(β-BL) homopolymer, which is attributed to increased water accessibility and surface hydrophilicity. The most pronounced decrease in molar mass, reaching at least 50% relative to the initial non-degraded sample, was observed for the diblock copolymers, whereas the P(β-BL) sample showed only a marginal weight reduction of a few percent. Overall, this study demonstrates that the combination of hydrophilic mPEG and PGl blocks with P(β-BL) enables the design of block copolymers with tunable thermal properties, solubility, and degradation behavior, offering potential for a wide range of applications. Full article

Buildings account for a significant share of global energy consumption and carbon emissions, creating an urgent need for advanced energy retrofit technologies. This review critically examines the role of plasma-modified textile polymer materials in improving the energy efficiency and durability of building retrofit systems. Various textile polymers, including polyester (polyethylene terephthalate, PET), polypropylene (PP), polytetrafluoroethylene (PTFE), polyamide (PA), and fiber-reinforced composites, are evaluated in relation to plasma surface engineering approaches, including atmospheric plasma, dielectric barrier discharge (DBD), and plasma jet treatment. Reported studies demonstrate that plasma treatment significantly alters surface morphology and chemistry, resulting in increased surface roughness, enhanced wettability, improved coating adhesion, and superior hydrophobic behavior. Water contact angles increased from approximately 70° to 145° depending on polymer type and plasma conditions, while reflective coating performance improved with solar reflectance enhancements of approximately 10–15%. Plasma-treated reflective roofing and shading textiles also showed reductions in building cooling energy demand of approximately 18–25% and roof temperature decreases of 10–15 °C. Furthermore, plasma-induced surface activation improved durability, ultraviolet (UV) resistance, and weather stability of textile membranes used in facade and roofing applications. The review also discusses industrial challenges related to scalability, plasma aging effects, energy consumption, and long-term performance. Plasma-modified systems demonstrate strong potential for multifunctional, lightweight, and sustainable building envelope technologies for future energy-efficient construction. Full article

To address wellbore instability and the technical challenges associated with high-density water-based drilling fluid loss control in deep shale gas formations of the Sichuan-Chongqing region in China, a novel nano-micro sealant designated CLG-Seal was synthesized via molecular structural optimization. The molecular structure of newly developed CLG-Seal exhibits distinct core–shell structural characteristics. The inorganic nano-silica constitutes the rigid core of CLG-Seal, which guarantees its plugging performance. The hydrophobically associating polymer which is coated on the surface of nano-silica constructs the flexible shell of CLG-Seal, endowing the CLG-Seal with excellent gel-forming capacity, adhesion film-forming capacity, deformability and perfect dispersibility. Transmission electron microscopy and scanning electron microscopy were employed to characterize the morphology of the CLG-Seal nanomicron-scale plugging agent. The sealing performance and underlying mechanisms of CLG-Seal were subsequently evaluated via particle plugging apparatus tests, displacement experiments, and etched glass micromodel simulations. Field trials conducted in the third section of Well WY3-2-3HF validated the application effectiveness of this agent in drilling fluid systems. The results indicate that the nano-micro sealant CLG-Seal exhibits a median particle size of D₅₀ is 146 nm, which can be modulated by adjusting the synthesis conditions. The nano-micro sealant CLG-Seal significantly mitigates fluid loss in low-permeability microfractures and fissures. Notably, a concentration of merely 3% is sufficient to achieve optimal nano-micro plugging performance. The results of the mechanism study indicate that while the CLG-Seal particles are close to each other, the polymer chains with flexible long chain structure which are coated on the surface of nano-silica constructs tend to be intertwined, forming a cross-linked network structure of gel film, thereby increasing the interaction between nano-micron particles and forming an impermeable plugging film. In addition, due to the nanoscale effect, the CLG-Seal has a strong tendency to adsorb onto the surface of shale rock through hydrogen bonding with the shale matrix. The hydrophobically associating polymer with high elastic modulus and excellent mechanical properties can enhance the pressure-bearing capacity of the filter cake through elastic deformation. Therefore, these nano-micron particles can form a strong sealing film on the filter cake and at the micropores of shale rock, thereby creating a dense mud cake on the outside of the shale formation. Field trial results demonstrate that the incorporation of the nano-micro sealant CLG-Seal into the drilling fluid for the third section of Well WY3-2-3HF reduced the PPA fluid loss to 4.6 mL. This value represents a substantial reduction compared to adjacent wells and signifies a remarkable improvement over the drilling fluids previously employed in the Longmaxi Formation of this block. Furthermore, the treated drilling fluid exhibited a superior filtration control pressure capacity of 10.5 MPa. The operation was completed successfully without any lost circulation or wellbore instability, and achieved a drilling footage of 42 h with an average penetration rate of 7.81 m/h. The mud weight was reduced by approximately 0.08–0.10 g/cm³ compared to offset wells. These results confirm the excellent application efficiency of the newly developed CLG-Seal in field operations. Full article

We present an optimized method for producing semiconducting polymer dots using a water–ethanol mixed antisolvent during nanoprecipitation. Compared to conventional Pdots made with pure water as the antisolvent, these newly produced Pdots exhibit simultaneously enhanced fluorescence efficiency and stability of particle size and emission spectra. These findings should be mainly attributed to an improved core–shell Pdots nanostructure formed by a sequential nanoprecipitation process. It offers Pdots a purer, more compact, and hydrophobic inner core, coated with a greater number of hydrophilic polyethylene glycol shells. This viewpoint is further reinforced by Förster energy-transfer efficiency in a fluorescence donor-acceptor Pdots system. The novelly prepared Pdots can better encapsulate small-molecular cargoes and more efficiently bioconjugate to targets. Consequently, it demonstrates improved specific immunofluorescence staining of microtubule structures in living cells. Full article

Efficient separation of Cu–Mo sulfide minerals from moraine materials remains a major challenge for low-grade, high-moraine Cu–Mo ores. Fine-grained muscovite induces severe slime coating and gangue entrainment, thereby markedly reducing flotation selectivity. In this work, a biodegradable polymer depressant, polyaspartic acid (PASP), was employed to regulate Cu–Mo sulfide flotation under muscovite interference conditions. Microflotation tests, particle size distribution analysis, zeta potential measurements, SEM-EDS observations, contact angle measurements, and XPS analyses were conducted to clarify the dispersion behavior, slime-coating mechanism, and selective adsorption characteristics of PASP. The results demonstrated that PASP selectively depressed muscovite at relatively low dosages while exerting negligible influence on the floatability of chalcopyrite and molybdenite. Notably, at a dosage of 15 mg/L, PASP reduced muscovite recovery by 43.07% and 31.23% more effectively than sodium silicate and sodium hexametaphosphate, respectively, demonstrating superior selective depression efficiency under moraine interference conditions. Particle size distribution and zeta potential analyses confirmed that PASP effectively weakened heterocoagulation and electrostatic attraction between muscovite and sulfide minerals, thereby suppressing slime coating and improving slurry dispersion stability. SEM-EDS and contact angle analyses further revealed that PASP significantly reduced muscovite deposition on sulfide mineral surfaces while maintaining the hydrophobicity of chalcopyrite and molybdenite. High-resolution XPS analysis further indicated that PASP adsorbed onto muscovite mainly through coordination between carboxylate groups and surface Al–OH sites, forming a stable hydrophilic adsorption layer. Overall, PASP provides a low-dosage, highly selective, and biodegradable depressant strategy for mitigating muscovite-induced slime coating and improving the flotation separation of Cu–Mo sulfide ores under moraine interference conditions. Full article

Flexible supercapacitors (SCs) have attracted considerable attention for wearable electronics, and developing high-performance electrolytes is critical for their practical application. While hydrogels have been widely investigated as solid electrolytes, studies on double-network (DN) hydrogel electrolytes specifically addressing the electrode–electrolyte interface stability under mechanical deformation remain relatively scarce. A major obstacle is maintaining a stable electrode–electrolyte interface under large mechanical deformation. Drawing inspiration from the mucus of a snail, which effectively adheres to various surfaces in challenging conditions, we present a self-healing xanthan gum/hydrophobically associated polyacrylamide/NaCl (XG/HPAAm/NaCl) hydrogel polymer electrolyte (HPE) that facilitates the creation of flexible SCs with improved mechanical and electrochemical properties. The optimized 2 wt% XG/HPAAm/0.4 M NaCl DN HPE exhibits a high ionic conductivity of 4.0 S/m, a tensile strength of 0.43 MPa, and an elongation at break of 11.7 mm/mm, along with a high adhesive energy of 254.7 J/m². The tough HPE was coated with a mixed adhesive of 502 cyanoacrylate glue and triethyl citrate (TEC) to create a surface coating resembling “mucus”, onto which activated carbon (AC)-modified carbon cloth (CC) electrodes (CC/AC) were affixed on both sides to construct the flexible SCs. Investigations into the HPE’s characteristics and the SCs’ electrochemical performance at various bending angles reveal that the “mucus-coating” HPE exhibits strong electrode adhesion and significantly improved electrochemical performance. The assembled flexible SC delivers a high specific capacitance of 249.3 F/g at 0.30 A/g, retains 73.4% of its initial capacitance after 20,000 cycles, and maintains 86.9% capacitance retention under 180° bending, outperforming SCs assembled with original HPEs in both performance and stability. This approach provides a versatile method for improving the interfacial properties between electrodes and HPEs, paving the way for innovative applications in robust, self-healing, and flexible devices. Full article

Membrane distillation (MD) is an attractive complementary technology to conventional desalination systems. Yet commercial uptake remains limited by membrane pore wetting, temperature polarisation, and material trade-offs. This review critically examines polymeric membranes and demonstrates that reported performance gains cannot be attributed to individual polymers or fillers alone, but rather to optimised structure–property interactions governing wetting resistance, mass transfer, and mechanical integrity. Through a comparative analysis of benchmark metrics (water flux, contact angle, and liquid entry pressure), we identify recurring failure mechanisms, including nanoparticle agglomeration, coating instability, and hydrophobicity-driven compromises in liquid entry pressure and durability. Moving beyond a descriptive summary of materials, this review introduces a predictive structure–property–performance framework that systematically links dominant operational limitations and targeted modification strategies. The analysis reveals that surface-localised, adhesion-controlled modifications outperform bulk approaches by preserving pore architecture while mitigating fouling and wetting risks. Key research priorities include validation under high-salinity conditions relevant to brine management, standardised environmental and leaching assessments of nanomaterials, scalable fabrication protocols supported by techno-economic considerations, and developments on bioinspired materials. By shifting focus from material novelty toward rational design principles, this review establishes actionable selection criteria to accelerate the translation of MD membranes from laboratory concepts to industrially viable desalination technologies. Full article

Herein, we describe a versatile synthetic strategy for constructing Prussian Blue (PB)-coated polymeric nanocapsules (PB@nanocapsules) with tunable sizes and controlled PB loading. A soft template was first formed from a miniemulsion composed of water/chloroform/hexadecane (94.55:5:0.2, w/w/w), using P4VP₈₂-b-PDMAA₁₈₀ as a stabilizer and varying amounts of P4VP homopolymer as a hydrophobe and additional reactive site provider. Crosslinked nanocapsules were obtained by adding 1,2-bis-(2-iodoethoxy)ethane (BIEE) as a crosslinker. The resulting nanocapsules exhibited average hydrodynamic diameters ranging from approximately 282 nm (without P4VP homopolymer) down to 58 nm (with 0.01 g P4VP homopolymer), as determined by DLS and TEM. Subsequently, sequential coordination with sodium pentacyanoammine -ferroate(II) hydrate (Na₃ [Fe(CN)₅NH₃]), followed by the addition of FeCl₃, yielded a uniform PB coating, as confirmed by the appearance of a characteristic absorption peak at 780 nm in the UV–Vis spectra and a CN stretching shift from 2060 to 2070 cm⁻¹ in FT-IR. TEM and HAADF-STEM with EDX mapping revealed the homogeneous distribution of Fe across the nanocapsule shells. The PB loading could be further controlled by varying the Fe³⁺ addition (5.0 × 10⁻³–4.5 × 10⁻² mmol), with higher loading improving thermal stability. This rational design provides a robust and generalizable platform for engineering polymer–inorganic hybrid nanostructures with tailored functionalities. Full article

Stone heritage deteriorates through physical, chemical, and biological processes driven by water, climate, and microbial colonization. Multifunctional polymeric coatings combining hydrophobic and antimicrobial moieties have emerged as a promising conservation strategy, yet a substantial gap remains between laboratory innovation and real-world performance. This review critically examines advances from 2021 to 2026, covering wetting theory, antimicrobial mechanisms, and material architectures, including molecularly integrated systems, Sol–Gel hybrids, nanocomposites, and layered systems. Long-term studies on the Aurelian Walls in Rome and stone in Reims show that biocidal efficacy typically declines within one to two years despite the chemical persistence of the coatings. In parallel, hydrophobic performance often deteriorates over time due to UV exposure, particulate deposition, and surface chemical changes, leading to increased wettability and reduced protective efficiency. Substrate porosity governs durability and visual compatibility (ΔE* < 5 threshold), while treatments can reshape microbial communities, favoring stress-tolerant meristematic fungi. Regulatory pressure on fluorinated compounds drives the development of more sustainable alternatives. Emerging directions include stimuli-responsive systems, self-healing materials, slippery interfaces, and precision polymer architectures. However, future progress will depend on tailoring formulations to major lithotypes, improving compatibility with porous substrates, and validating performance through standardized accelerated aging and multi-year field trials. Bridging laboratory design with environmental exposure data and conservation practice will be essential for achieving durable and culturally acceptable protection strategies. Full article