Search Results (493)

The food packaging sector widely relies on polymeric materials, and as sustainability concerns grow, commodity polymers need to be replaced with innovative and more sustainable materials. Thermoplastic polyurethane (TPU) is a versatile elastomeric polymer characterized by flexibility, strength, chemical and abrasion resistance, and biocompatibility. However, it presents some limitations, notably in terms of functional properties (such as barrier properties). The use of nano-sized renewable fillers, such as cellulose nanocrystals (CNCs), may improve these properties, extending the applicability range of TPU. In this work, bio-based TPU nanocomposites were obtained by adding commercial silane-modified cellulose nanocrystals (Si−O−CNC) at different contents (1–5 wt.%). The nanocomposites were produced via melt mixing followed by compression molding and were characterized in terms of their chemical (FTIR), morphological, thermal, mechanical, rheological, wettability, and barrier properties (i.e., water vapor permeability, WVP and oxygen transmission rate, OTR). The presence of Si−O−CNC promoted hydrogen-bonding interactions with the TPU matrix, affecting the microphase separation and organization of the hard segments. These microstructural changes improved thermal stability, reduced WVP and OTR, and increased tensile properties at lower nanofiller contents (1–3 wt.%). At higher contents, partial nanofiller aggregation was observed, leading to a reduction in mechanical performance. Overall, these results suggest that TPU/Si−O−CNC nanocomposites have promising potential as sustainable food packaging materials. Full article

Silicon is among the most abundant elements on Earth, yet its incorporation into organic molecules is atypical in most biological contexts. However, the strategic introduction of silicon, in line with the demonstrated success of the incorporation of other bio-orthogonal elements, has emerged as a powerful approach in medicinal chemistry, enabling access to small molecules with unique chemical, physical, and biological properties that offer improved potency, stability, tolerability, or bioavailability profiles for the discovery and development of anticancer therapeutics. In this review, we describe the direct connection between reactivity and physiochemical paradigms of different classes of organosilicon-containing functional groups and their strategic deployment in small molecule design, including silanes, silyl ethers, siloxanes, and organosilicates. Specifically, we aimed to demonstrate how these strategies can be informed by first principles of reactivity in organosilicon containing functional groups, in both synthetic small molecules and bioactive natural products. Particular emphasis is placed on how silicon replacement and addition can be leveraged beyond simple isosteric carbon replacement, and how consequent structure–activity relationships arising from installation of diverse organosilicon motifs can also serve a unique role in unveiling new aspects of biological mechanism and function. Ultimately, the growing body of literature in applications of organosilicon-containing anticancer small molecules and the increasing sophistication and selectivity of synthetic methods used to construct these motifs will undoubtedly continue to expand the appreciation of organosilicon-based functional groups in the medicinal chemist’s toolbox. Full article

Advanced oxidation processes using titanium dioxide (TiO₂) have emerged as a promising approach for the photocatalytic degradation of contaminants in water and have drawn extensive research attention despite limited translation of this technology to large-scale applications. The limitations of this technology include immobilization of the photocatalyst, scalability, and compatibility with available light sources. Using 3D printing to immobilize TiO₂-based photocatalysts, we systematically evaluated the rates of photocatalytic degradation of methylene blue (MB) with different light-emitting diode (LED) ultraviolet (UV) light sources and modified TiO₂-based photocatalytic materials. The UV LED lights successfully decreased the MB concentrations with half-lives ranging from 0.9 to 2.4 h, with relative photocatalytic performance of UVA-365 > UVA-395 > UVC-280. The photocatalytic degradation rates under UV LEDs were slower (0.9–2.4 h) than those achieved using a low-pressure mercury UV-C lamp (0.5 h) and were also lower than those observed under solar simulated lights (0.6 h). The TiO₂ modified by an alkyl silane entity and embedded in a polylactic acid polymeric system with 3D printing exhibited the fastest methylene blue (MB) removal among the three TiO₂-based structures evaluated, with a half-life of 0.6 h compared to the 1.6–17.7 h for the other materials. This research demonstrated that 3D printing enables the integration of functionalized photocatalysts, and, when paired with low-cost, low-energy UV LED lights, can achieve environmentally relevant rates of performance. Ultimately, these findings represent an incremental step toward improving the performance of 3D-printed photocatalytic materials. Full article

Polymer electrolyte membranes serving in proton exchange membrane fuel cells (PEMFCs) and direct methanol fuel cells (DMFCs) must possess sufficient mechanical–dimensional stability and excellent proton conducting capacity. Derived from the successful syntheses of two different sulfonated poly(aryl ether ketone)s bearing functional amine groups, two series of novel epoxy-crosslinked and silane-crosslinked sulfonated poly(aryl ether ketone) electrolyte networks are constructed for highly conductive and mechanically stable proton exchange membranes. The designed multi-component architecture, which integrates a moderate-ion-exchange-capacity sulfonated poly(aryl ether ketone) (moderate-IEC SPAEK), a high-IEC SPAEK, and a tailored crosslinker (epoxy or silane), enables a breakthrough in decoupling the traditional trade-off between conductivity and stability. The resulting membranes exhibit an outstanding combination of properties: exceptional proton conductivity exceeding 0.18 S cm⁻¹ at 100 °C, tensile strength above 28.80 MPa, and enhanced chemical resistance, thermo-oxidative stability, and competitive direct methanol fuel cell performance. This work establishes a rational design strategy for crosslinked multi-component membranes as a promising platform for next-generation high-performance fuel cells. Full article

Photovoltaic modules require efficient sunlight modulation, including enhanced visible transmittance and conversion of unused ultraviolet light. This study develops a synthetic optical coating that achieves both functions by integrating down-conversion BAM (BaMgAl₁₀O₁₇:Eu²⁺, Mn²⁺) nanophosphors into a silica anti-reflection sol. The key novelty lies in a synergistic surface engineering strategy that decouples dispersion stabilization from luminescence protection. Five dispersants are systematically compared under combined ball and sand milling. The polyester-modified acrylic long-chain dispersant (DK062) yields a stable nanodispersion with an average particle size of 228 nm and a Zeta potential of −7.61 mV, effectively suppressing re-agglomeration while retaining high photoluminescence. Subsequent surface modification with KH570 grafts a dense silane passivation layer via Si–O–M covalent bonds, further increasing the photoluminescence intensity by 1.39-fold. The optimized nanophosphors are incorporated into a commercial anti-reflection sol and dip-coated onto photovoltaic glass. At a doping concentration of 2‰ and a withdrawal speed of 8 mm/s, the resulting DCSAR coating exhibits an average transmittance of 91.16%—slightly higher than that of the pure anti-reflection coating (90.96%)—while showing strong green emission at 515 nm. Industrial on-site testing further demonstrates an average transmittance of 94.20%–94.31% with uniform green emission. This work provides a scalable route to fabricate highly transparent, light-converting anti-reflection coatings by combining dispersant-assisted milling and silane passivation. Full article

Fluoroalkyl-substituted organoboron compounds are valuable building blocks for organic synthesis and for the development of functional molecules in medicinal chemistry, agrochemicals, and materials science. Building on our previous work on difluoromethyl-substituted borates, we report the synthesis and structural characterization of trifluoromethylated borates, 2-aryl-4,4,5,5-tetramethyl-2-(trifluoromethyl)-1,3,2-dioxaborolan-2-uide salts ([pinB(Aryl)CF₃]⁻). Treatment of pinB–Aryl boronates (pinB = 4,4,5,5-tetramethyl-1,3,2-dioxaborolane) with trimethyl(trifluoromethyl)silane (Ruppert–Prakash reagent) in the presence of potassium tert-butoxide and 18-crown-6 ether (18-C-6) afforded the corresponding trifluoromethylated borates as isolable crystalline compounds. Compared with the related difluoromethylated borates, the CF₃ substituent increases the tendency of [pinB(Aryl)CF₃]⁻ to exhibit hygroscopic behavior, as supported by a hydrated crystal structure and the formation of a hygroscopic product. The isolable trifluoromethylborates can serve as reservoirs of electrophilic trifluoromethyl radicals upon oxidation. Full article

Heavy metal contamination in water remains a major environmental concern due to the persistence, toxicity, and bioaccumulation potential of metal ions such as Ni²⁺ and Cu²⁺. Therefore, the development of sustainable membrane materials with improved permeability and metal ion retention capacity is of significant interest for advanced water purification applications. In this research, crown ether-functionalized cellulose acetate membranes were developed by employing cyanuric chloride as a linker in order to enable advanced heavy metal ion retention capacity. In order to achieve this, the modification process involved a multi-step approach comprising successive hydroxylation, silanization, triazine activation, and crown ether grafting. The successful functionalization was confirmed by FTIR (Fourier Transform Infrared Spectroscopy) and XPS (X-ray Photoelectron Spectroscopy) analyses, while thermal characterization demonstrated improved stability over a wide range of temperatures without compromising the integrity of the cellulose acetate backbone. The crown-ether-functionalized membranes exhibited enhanced performance in terms of heavy metal ion separation, demonstrating significantly higher retention of Ni²⁺ (30%) and Cu²⁺ (27%) as compared to pristine CA membranes (<10%) over repeated filtration cycles. These results demonstrate that crown ether functionalization is a versatile approach for tuning the interfacial features of cellulose acetate membranes in order to achieve increased permeability and selectivity toward heavy metal removal, highlighting their potential for advanced water purification applications. Full article

The growing demand for sustainable packaging materials has accelerated interest in biomass-derived carbon fillers as functional reinforcements for biodegradable polymer composites. This review critically evaluates the use of carbon materials produced from agricultural residues, particularly palm kernel shell (PKS) and coconut shell (CS), in biopolymer composite coating films for food packaging applications. Recent thermochemical conversion routes, including carbonization, activation, and catalytic graphitization, are discussed in relation to their influence on filler morphology, porosity, surface chemistry, and graphitic ordering. Particular emphasis is placed on structure–property relationships in composite systems containing matrices such as polylactic acid (PLA), starch, chitosan, gelatin, and polyvinyl alcohol (PVA). Published studies indicate that properly dispersed carbon fillers can improve tensile strength, thermal stability, ultraviolet shielding, and oxygen/water vapor barrier performance through stress-transfer mechanisms and tortuous diffusion pathways. However, excessive filler loading or poor interfacial compatibility frequently causes agglomeration, brittleness, and loss of transparency. Surface modification strategies including oxidation, silanization, and surfactant-assisted dispersion, are therefore reviewed as key approaches to optimize composite performance. Finally, current limitations involving migration safety, process scalability, and the lack of standardized testing protocols are discussed. Overall, PKS- and CS-derived carbon fillers represent promising sustainable additives for next-generation biopolymer composite packaging systems. Full article

In the surface protection of stone and brick cultural heritage, a primary challenge is that traditional polymeric coatings are prone to photooxidative degradation under ultraviolet (UV) irradiation, and the resulting aged fragments readily block the substrate micropores, leading to a loss of “breathability”. To address the performance conflict among waterproofing, breathability, and weather resistance, this study prepared few-layer Ti₃C₂T_X MXene using a minimally intensive layer delamination (MILD) method. The poor compatibility between MXene and the fluorosilicone (FPS) resin matrix was effectively resolved through covalent modification with a silane coupling agent (KH-550). Results demonstrate that at an ultralow loading (0.5 wt%), the functionalized f-MXene is uniformly dispersed within the resin. This structure not only spontaneously constructs a hierarchical rough architecture on the surface that imparts high hydrophobicity (water contact angle of 131.6°), but its internal “labyrinth effect” also effectively blocks corrosive media. Simultaneously, the intrinsic water vapor transmission rate of the substrate is effectively maintained (with a reduction of less than 3%), and no visually perceptible color difference is generated (∆E = 1.2). Mechanically, f-MXene relies on interfacial interactions to act as a “nano-skeleton” for stress transfer, thereby increasing the uniaxial compressive strength of fragile limestone by 32.4%. Optical and spectroscopic characterizations further elucidate its anti-aging mechanism: f-MXene not only provides broadband UV shielding but also exhibits highly efficient radical scavenging activity during long-term UV aging. After 400 h of aging, the concentrations of hydroxyl and superoxide anion radicals within the system are significantly reduced, blocking the photooxidative chain reaction from the source. This work develops a composite protective material system for stone cultural heritage that simultaneously integrates high moisture permeability, minimal visual intervention, and long-term antioxidant performance. Full article

The linear economic model continues to drive multidimensional environmental problems, as it generates large volumes of plastic waste, as well as agricultural by-products, such as coconut husks. On the other hand, the maritime industry still relies on conventional materials such as wood, steel, and fibre-reinforced plastics, which have several usage challenges, including corrosion, toxicity, and difficulties associated with end-of-life management. These issues point to the need for more sustainable material options. This review examines the potential of combining coconut fibre (coir) with recycled plastics to produce a functional material for use in the maritime sector. The material is designed to add value to waste streams by providing a practical approach to reducing dependence on conventional and less sustainable resources. The review discusses fibre treatments (alkali, silane, acetylation) and fabrication methods (compression moulding, extrusion) and evaluates their impact on mechanical performance and durability. The studies show that coir–plastic composites possess highly tuneable mechanical properties. Tensile strengths are reported to range from approximately 2.4 MPa for natural resin matrices to 78 MPa for polyester hybrids, while the flexural modulus can be increased by up to 99% compared to the neat polymer blend. Fibre treatments (e.g., alkali) and fabrication methods are crucial, as they have been shown to improve tensile and flexural strength by over 40% and impact strength by 150%. However, the composites produced still show vulnerability to water absorption, UV radiation, and biofouling, which could limit their application in marine environments. To this end, several issues require further study, including long-term field validation, enhanced understanding of material fatigue, and scalable manufacturing. Full article

Ice accumulation on aircraft surfaces severely affects aerodynamic performance by increasing drag and reducing lift, leading to stall conditions. Conventional thermal and pneumatic anti-/de-icing systems, although widely used, have some disadvantages, including high cost, inefficiency, and environmental unsustainability. Hydrophobic and icephobic coatings have emerged as a promising alternative to reduce ice adhesion and delay ice formation. This paper reviews the use of silane agents in epoxy-based coatings, incorporating functional additives such as natural fibers, quantum dots, and nanoparticles, to enhance hydrophobicity. Results demonstrated that the combination of silanes and functional additives affects surface features and wettability, improving hydrophobicity. These case studies show the potential of this approach in the development of coatings for advanced aircraft ice-protection applications. Full article

Thyroxine (T4) is a key hormone regulating metabolic, cardiovascular, and neurodevelopmental processes, yet its clinical quantification still relies on centralized immunoassays that limit rapid or point-of-care monitoring. Here, we present a label-free biosensing platform based on silicon nanowire field-effect transistors (SiNW-FETs) functionalized with a T4-selective DNA aptamer via a 3-Triethoxysilyl propylsuccinic Anhydride (TESPSA)-mediated silanization approach, enabling a streamlined two-step modification for oriented immobilization. The biosensor achieves robust real-time detection of T4 across the physiological concentration range (5–30 pM), with a limit of detection of ~5 pM and a strong linear correlation between drain current and analyte concentration (R² = 0.9931). Specificity is confirmed using non-functionalized devices and estradiol as a non-target control. All measurements were performed in undiluted phosphate-buffered saline, representing a physiologically relevant ionic environment and demonstrating stable sensor performance under realistic buffer conditions. The dose–response behavior follows a Hill model, allowing extraction of binding parameters and confirming that the electrical signal originates from specific aptamer–target interactions. These results demonstrate that aptamer-functionalized SiNW-FETs provide a highly sensitive, selective, and miniaturizable platform for quantitative thyroid hormone monitoring, with strong potential for future point-of-care applications. Full article

In this work, various types of organosilanes were introduced into Sn-Si oxide through a simple aerosol process to yield synthesis precursors. Then, a series of Sn-Beta zeolites were successfully synthesized using a hydrothermal method in the presence of fluoride. The influence of amine groups (A, 2A, and 3A), the length of branched chains present in the organosilanes, as well as the use of dipodal silanization agents (B2A) on the morphology, pore structure, acidic properties, coordination state, and content of Sn species in the obtained Sn-Beta zeolite samples was investigated. Compared to the organosilane-free Sn-Beta (crystal size: 1.3 μm; Si/Sn = 119; Lewis acid density: 77 μmol·g⁻¹), all monopodal organosilane-doped samples (Sn-Beta-A, -2A, and -3A) exhibited reduced crystal sizes (~0.9 μm) and increased specific surface areas (up to 502 m²·g⁻¹ for Sn-Beta-2A). UV–Vis spectroscopy showed that Sn-Beta-2A (containing two amine groups) achieved the highest optical bandgap (4.68 eV) and the strongest suppression of extra-framework SnO_x species (peak at ~269 nm), indicating the most isolated tetrahedral framework Sn⁴⁺ sites. This sample also delivered the highest Lewis acid density (225 μmol·g⁻¹) and the best catalytic performance in the Baeyer–Villiger oxidation of cyclohexanone (39% conversion, TON = 106) and 2-adamantanone (37% conversion, TON = 101). By contrast, the dipodal organosilane (B₂A) caused severe steric hindrance, yielding the lowest crystallinity (relative crystallinity 64%), Si/Sn ratio (158), Lewis acid density (38 μmol·g⁻¹), and catalytic activity, despite forming a nanoaggregate morphology with high mesoporosity (V meso = 0.20 cm³·g⁻¹). These quantitative results demonstrate that monopodal organosilanes with two amine groups optimally balance Sn incorporation and textural properties, whereas dipodal silanes hinder framework Sn entry. This study provides clear, numerically grounded guidelines for selecting organosilane functional groups to design high-performance Sn-Beta zeolites. Full article

Superhydrophobic coatings are regarded as a promising passive anti-icing strategy; however, their practical engineering application, particularly in electrical insulation, is severely hindered by the performance deterioration caused by mechanical damage and a lack of theoretical understanding of microscopic ice adhesion mechanisms. In this study, a layered polymer composite coating was designed to resolve the trade-off between abrasion resistance and low ice adhesion. The chemistry of the coating relies on a synergistic “primer–topcoat” design: the primer consists of an epoxy resin matrix chemically modified by amino silicone oil to lower its surface energy and improve toughness, while the topcoat features hierarchical SiO₂ clusters functionalized with hexamethyldisilazane (HMDS) and silane coupling agents. This architecture was fabricated via a controllable layer-by-layer spraying method. Systematic investigations revealed that the hierarchical micro/nanostructure, composed of microscale protrusions and nanoscale SiO₂ clusters, provides excellent superhydrophobicity (contact angle of 155.2°, sliding angle of 2°). Crucially, the crosslinked polymer network and stable siloxane (Si-O-Si) covalent bonding ensure that the coating maintains its functionality after a cumulative sand impact of 3 kg, demonstrating superior mechanical durability. Furthermore, differentiated theoretical models for ice adhesion in Cassie–Baxter and Wenzel states were established based on intermolecular interactions, identifying that maintaining a stable Cassie–Baxter state is key to reducing adhesion. This study offers a robust approach to balancing functionality and durability in polymer composites through synergistic structural design, providing both a scalable fabrication strategy and a quantitative theoretical framework for understanding interfacial ice adhesion. Full article

To enhance the mechanical properties and waterproof performance of polymer–cement (JS) waterproof coatings, cellulose nanofibrils (CNFs) were surface-modified using vinyltriethoxysilane (VTES). The modified cellulose nanofibrils (m-CNFs) were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) analysis, and energy-dispersive X-ray spectroscopy (EDS). JS waterproof coatings incorporating m-CNFs were subsequently prepared. The performance and mechanism were systematically evaluated using the tensile strength, bonding strength, water absorption, contact angle, permeability test, durability test, scanning electron microscopy, Brunauer–Emmett–Teller (BET) and atomic force microscopy (AFM). The results indicated that the coating exhibited optimal performance when 1 wt% m-CNFs were incorporated. Under this condition, the tensile strength and bonding strength increased by 33.8% and 9.8%, respectively, while the 7-day water absorption decreased by 72.9%. The contact angle reached 97.1°, and the durability of the coating was also improved. Moreover, the amphiphilic nature introduced by silane modification effectively improved the interfacial adhesion between the organic and inorganic phases within the coating. In addition, due to their water absorption capacity, m-CNFs fill the micropores of the coating during the curing process and produce an internal curing effect, thereby reducing the porosity of the material. As a result of these synergistic effects, the mechanical strength and hydrophobicity of the JS waterproof coating are significantly enhanced. This study expands the application of CNFs, a sustainable nanomaterial, in building waterproofing materials. Full article