Polymer Matrix Research Articles

Significantly Enhanced Thermal Conductivity of hBN/PTFE Composites: A Comprehensive Study of Filler Size and Dispersion.

High-temperature polymers are attractive for applications in extreme temperatures, where they maintain their mechanical flexibility and electrical insulating properties. However, their heat dissipation capability is limited due to their intrinsically low thermal conductivities. Hexagonal boron nitride (hBN) is a chemically inert, thermally stable, and electrically insulative compound with a high thermal conductivity, making it an ideal candidate as a filler within a high-temperature polymer matrix to increase the thermal conductivity. This study evaluates the effect of filler size and dispersion on thermal conductivity by producing homogeneous composite samples using a combination of solvent mixing and resonant acoustic mixing (RAM). We carefully characterized our samples, including the spread of the size distribution, and observed that the smaller sized hBN centered around 5 μm was able to integrate more seamlessly into the polytetrafluoroethylene (PTFE) matrix with particle size in the 15 μm range and hence outperformed 30 μm, in contrast to the conventional wisdom, which asserts that larger fillers universally perform better than smaller ones. Our thermal conductivity of hBN/PTFE composites at 30 wt % is 2× higher than the literature values. Notably, we reached the record-high value of 3.5 W/m K at 40 wt % with an onset of percolation at 20 wt %, attributed to optimized hBN dispersion that facilitates the formation of thermal percolation. Our findings provide general guidelines to enhance the thermal conductivity of polymer composites for thermal management, ranging from power transmission to microelectronics cooling.

Influence of Dry-Mixing and Solvent Casting Blending Techniques on the Mechanical and Biological Behavior of Novel Biocompatible Poly(ε-caprolactone)/Alumina-Toughened Zirconia Scaffolds Obtained by 3D Printing

This work focuses on the study and comparison of two mixing methods for the dispersion of Alumina-Toughened Zirconia (ATZ) within the polymer matrix of Poly(ε-caprolactone) (PCL). The dry-mixing method using solvent-free impact milling (M) and the solvent casting method with chloroform (SC) were investigated. Samples were produced by 3D printing, and specimens were printed at increasing ATZ loadings (namely, 10, 20, and 40 wt.%). The chemico-physical, mechanical, and cell interaction characteristics of the materials prepared with both mixing methods were studied. Solvent mixing allowed better dispersion of the ATZ in the polymer matrix with respect to dry mixing. In addition, dry mixing affected the molecular weight of the PCL/ATZ composites much more than the solvent casting method. For these reasons, materials obtained by solid mixing exhibited the worst mechanical performance with respect to those obtained by solvent casting, which showed increased Young’s moduli with increasing ATZ amounts. The in vitro biological response elicited in a mesenchymal stem cell model seemed to be influenced by the mixing method, with a preference for the composites obtained through solvent mixing and containing 20 or 40 wt.% of ATZ.

Influence of wax addition on feedstock processing behavior in additive manufacturing of metals by material extrusion

AbstractThe additive manufacturing of metals by material extrusion in a multi-step process (MEX-MSt/M) represents a special process variant of the commonly used material extrusion (MEX) and is based on the processing of highly filled polymer filaments. This technology uses the geometrical freedom and fast processing given by MEX to create individual metal parts after a debinding and sintering process in a cost and time-efficient way. The filaments for MEX-MSt/M are made by incorporating metal powders, such as aluminum, stainless steel, or bronze into a polymer matrix. Due to the challenges that are assigned to the processing of highly filled polymers, like the increased viscosity of the material or clogging of the nozzle, the binder materials have to meet several requirements. Therefore, waxes are often used to enable a better extrusion behavior for MEX; however, the addition of wax also affects other crucial processing properties of the filaments. In this work, the interactions of different types and amounts of waxes on thermal, mechanical, and rheological properties were investigated to create a better understanding of the alternating effects of wax addition into highly filled filaments for processing via MEX. The study demonstrated that an increase in wax contents resulted in both a significant decrease in ductility and an overall improvement in melt flowability. The choice of waxes also affected the particle–matrix interactions, partly leading to an improved wetting of the filler particles.

Advanced Polymer Composite with Graphene Content for Emi Shielding

One of the increasingly common unexpected outcomes of the extensive usage of electronic devices and systems is electromagnetic interference (EMI). The need for efficient fillers and shielding materials to manage electromagnetic interference (EMI) and associated issues is rising. Adding more filler typically means greater production costs, poor dispersion, and unintended agglomeration, which makes polymer composites harder to work with and mechanically weak. Therefore, it is highly desired to design a strong composite with conductive filler content that nonetheless performs well as an EMI shield. Therefore, using a graphene substrate and dispersion of conducting polymers such as polyacetylene and MWCNT fillers, a hybrid polymer composite based on polyetherimide is proposed in this research. Next, the enhancement of EMI shielding efficiency is examined. The design of the graphene substrate was completed with a coating based on nano filler, and the blending methods of the polymer matrix and the reinforcing filler materials are explored. ANSYS-HFSS software is then used to assess the shield's efficacy among others, and the results demonstrated improved performance. Therefore, by putting the suggested design into practice, high-performance EMI shielding materials can be created by combining various shield fillers. As a result, the composites' mechanical, electrical, and EMI shielding qualities will all improve.

High-Resolution X-ray Image from Copper-Based Perovskite Hybrid Polymer.

Cs3Cu2I5 nanocrystals (NCs) are considered to be promising materials due to their high photoluminescence efficiency, lack of lead toxicity, and X-ray responsiveness. However, during the crystallization process, NCs are prone to agglomeration and exhibit uneven size distribution, resulting in several light scattering that severely affect their imaging resolution. Herein, we successfully developed a high-resolution scintillator film by growing copper-based perovskite NCs within a hybrid polymer matrix. By leveraging the ingenious integration of polyvinylidene fluoride (PVDF) and polymethyl methacrylate (PMMA), the size and distribution uniformity of Cs3Cu2I5 NCs can be effectively controlled. Consequently, a high spatial resolution of 14.3 lp mm-1 and a low detection limit of 105 nGy s-1 are achieved, and the scintillator film has excellent flexibility and stability. These results highlight the promising application of Cs3Cu2I5 scintillator films in low-cost, flexible, and high-performance medical imaging.

Understanding Na+ Diffusion, Physicochemical Behavior, and Electrochemical Performance of a Gel Polymer Electrolyte.

Gel polymer electrolytes (GPEs) represent a credible alternative to organic liquid electrolytes (LEs) for safer sodium metal batteries. As a compromise between solid polymer electrolytes and LEs, GPEs ensure a good ionic conductivity, improve the electrolyte/electrode interface, and prevent solvent leaks. Herein, a GPE based on acrylate-bifunctionalized polyethylene glycol chains mixed with an ether solvent (TEGDME) and a polyethylene glycol diacrylate (PEG600DA) in a 50/50 wt % ratio was prepared by ultraviolet photopolymerization. Sodium bis(fluorosulfonyl)imide salt (NaFSI) was added at different concentrations to study its interactions with the solvent and/or the cross-linked polymer. Infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry, and swelling ratio characterizations were combined to determine the physicochemical properties of the GPE. Complementary characterizations including electrochemical impedance spectroscopy, chronopotentiometry, and cyclic voltammetry allowed correlating the physicochemical properties of the GPE to its electrochemical performance. Then, improvements were obtained by careful combination of its components. The cross-linking agent allowed us to obtain a polymer matrix that traps the organic solvent and prevents leakage. Such a solvent inclusion reduces the rigidity of the membrane and lowers its viscosity, offering a room temperature ionic conductivity of 4.8 × 10-4 Ω-1 cm-1. The control of polymer's tortuosity leads to a stable cycling vs sodium metal over several hundred hours without increase of the polarization. Finally, optimization of the salt loading plays a major role in electrostatic cross-linking, leading to an improvement of the mechanical properties of the GPE without reducing its conductivity.

High green index electromagnetic interference shields with semiconducting Bi2S3 fillers in a PEDOT:PSS matrix.

Conventional metallic electromagnetic interference (EMI) shields, as well as the emerging 2D material-based shields, meet the shielding effectiveness (SE) needs of most applications. However, their shielding performance is dominated by the reflection of incoming radiation due to their high electrical conductivity, which leads to secondary pollution. This problem is getting exacerbated with the proliferation of electronics and communication networks in modern society. Thus, EMI shields that function dominantly by the absorption of incoming radiation are highly desirable. Such shields would be characterized by a green index, which is the ratio of absorbance over reflectance, close to or greater than one. For nonmagnetic materials, the best way to reduce the undesirable large impedance mismatch is to reduce the effective permittivity of the shield material. Here, we present a new EMI shield with a semiconductor Bi2S3 filler in a conducting PEDOT:PSS polymer matrix, instead of the conventional conductive fillers, to reduce the effective permittivity and demonstrate that even a light loading of only 10% Bi2S3 provides high SE of over 40 dB with a green index value of 0.75. Increasing the filler content to 15 wt% increases the green index close to unity while dropping the SE to 30 dB. The shielding mechanism is explained through electromagnetic parameter measurements and supplemented by density functional theory calculations. This work lays the foundation for the advancement of lightweight and ultrathin green EMI shields with minimum secondary pollution.

Lightweight, Strong, and Transparent Wood Films Produced by Capillary Driven Self-Densification.

Wood delignification and densification enable the production of high strength and/or transparent wood materials with exceptional properties. However, processing needs to be more sustainable and besides the chemical delignification treatments, energy intense hot-pressing calls for alternative approaches. Here, this study shows that additional softening of delignified wood via a mild swelling process using an ionic liquid-water mixture enables the densification of tube-line wood cells into layer-by-layer sheet structures without hot-pressing. The natural capillary force induces self-densification in a simple drying process resulting in a transparent wood film. The as-prepared films with ≈150µm thickness possess an optical transmittance ≈70%, while maintaining optical haze >95%. Due to the densely packed sheet structure with a large interfacial area, the reassembled wood film is fivefold stronger and stiffer than the delignified wood in fiber direction. Owing to a low density, the specific tensile strength and elastic modulus are as high as 282MPacm3g-1 and 31GPacm3g-1. A facile and highly energy efficient wood nanotechnology approach are demonstrated toward more sustainable materials and processes by directly converting delignified wood into transparent wood omitting polymeric matrix infiltration or mechanical pressing.

Exploring the Impact of Reinforcing Filler Systems on Devulcanizate Composites

Composites revolutionize material performance, fostering innovation and efficiency in diverse sectors. Elastomer-based polymeric composites are crucial for applications requiring superior mechanical strength and durability. Widely applied in automotives, aerospace, construction, and consumer goods, they excel under extreme conditions. Composites based on recycled rubber, fortified with reinforcing fillers, represent a sustainable material innovation by repurposing discarded rubber. The integration of reinforcing agents enhances the strength and resilience of this composite, and the recycled polymeric matrix offers an eco-friendly alternative to virgin elastomers, reducing their environmental impact. Devulcanized rubber, with inherently lower mechanical properties than virgin rubber, requires enhancement of its quality for reuse in a circular economy: considerable amounts of recycled tire rubber can only be applied in new tires if the property profile comes close to the one of the virgin rubber. To achieve this, model passenger car tire and whole tire rubber granulates were transformed into elastomeric composites through optimized devulcanization and blending with additional fillers like carbon black and silica–silane. These fillers were chosen as they are commonly used in tire compounding, but they lose their reactivity during their service life and the devulcanization process. Incorporation of 20% (w/w) additional filler enhanced the strength of the devulcanizate composites by up to 15%. Additionally, increased silane concentration significantly further improved the tensile strength, Payne effect, and dispersion by enhancing the polymer–filler interaction through improved silanization. Higher silane concentrations reduced elongation at break and increased crosslink density, as it leads to a stable filler–polymer network. The optimal concentration of a silica–silane filler system for a devulcanizate was found to be 20% silica with 3% silane, showing the best property profile.

Polymer Matrix and Manufacturing Methods in Solid Dispersion System for Enhancing Andrographolide Solubility and Absorption: A Systematic Review.

Background: Andrographolide (ADG) has poor aqueous solubility and low bioavailability. This study systematically reviews the use of solid dispersion (SD) techniques to enhance the solubility and absorption of ADG, with a focus on the methods and polymers utilized. Methodology: We searched electronic databases including PubMed, Web of Science, Scopus®, Embase and ScienceDirect Elsevier® up to November 2023 for studies on the solubility or absorption of ADG in SD formulations. Two reviewers independently reviewed the retrieved articles and extracted data using a standardized form and synthesized the data qualitatively. Results: SD significantly improved ADG solubility with up to a 4.7-fold increase and resulted in a decrease in 50% release time (T1/2) to less than 5 min. SD could also improve ADG absorption, as evidenced by higher Cmax and AUC and reduced Tmax. Notably, Soluplus-based SDs showed marked solubility and absorption enhancements. Among the five SD techniques (rotary evaporation, spray drying, hot-melt extrusion, freeze drying and vacuum drying) examined, spray drying emerged as the most effective, enabling a one-step process without the need for post-milling. Conclusions: SD techniques, particularly using Soluplus and spray drying, effectively enhance the solubility and absorption of ADG. This insight is vital for the future development of ADG-SD matrices.

Fabrication and Characterization of Natural Fiber-Polymer Composites for Prosthesis Socket Application

ABSTRACT A natural fiber-reinforced composite from a locally available false banana plant is developed for a prosthesis socket application. Four batches of composite samples are fabricated by arranging the longitudinal uniformly distributed unidirectional false banana fibers in four orientations (0°, 90°, ±45°, 0°/90o). The composites’ mechanical and physical properties, such as tensile strength, compression strength, flexural strength, impact resistance, and the effect of chemical treatment on water absorption, are investigated. The results are compared with E-glass fiber-reinforced polymer matrix composite. The false banana fiber-polymer composites with a 0° fiber orientation have a tensile strength of 86.81 MPa, less than 9% lower than E-glass-fiber composites (95.44 MPa), and an impact resistance of 6.25 J, 10% higher compared to the E-glass fiber polymer composites (5.70 J). In addition, the treated false banana fiber-polymer composite absorbed 70% less water than the untreated false banana fiber-polymer composite. It is observed that the fiber treatment has increased the polymer–fiber interaction and the interface strength of the false banana fiber-polymer composites.

Enhanced polyacrylamide polymer hydrogels using nanomaterials for water shutoff: Morphology, thermal and rheological investigations at high temperatures and salinity

This study focuses on the synthesis, characterization, and performance evaluation of polyacrylamide (PAM)/polyethyleneimine (PEI) hydrogels enhanced with nanomaterials for potential application in conformance control in oil wells. The materials used include PAM with a molar mass of 25,000 Kg mol−1, PEI with an average weight molar mass of 25 Kg mol−1, and synthetic brine (ionic strength 0.6). Nanomaterials such as titanium dioxide (TiO2) nanoparticles, oxidized carbon nanotubes (CNT-ox), and graphene oxide (GO) were incorporated into the hydrogel matrix. A simple method was used for the incorporation of nanomaterials into the polymeric matrix, ensuring their good dispersion in the hydrogels formed. Characterization techniques including thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) were employed to analyze the structure, morphology, and thermal stability of the hydrogels. Rheological measurements and gel strength evaluations were conducted to assess the performance of the hydrogels. Results indicate that the incorporation of nanomaterials enhanced the thermal stability, gel strength (Sydansk code), and resistance to syneresis of the hydrogels. Specifically, the addition of TiO2 nanoparticles exhibited the highest improvement in viscosity and thermal stability, attributed to strong interactions between TiO2 and PAM molecules. A notable decrease in syneresis percentages was observed with the inclusion of nanomaterials compared to the PAM reference sample, reaching 70.1 % for the hydrogel modified with GO. These findings suggest that nanomaterial-enhanced hydrogels hold promise for applications in conformance control in oil wells, offering improved stability and performance over extended periods of use.

Hydrophilic Photocrosslinkers as a Universal Solution to Endow Water Affinity to a Polymer Photocatalyst for an Enhanced Hydrogen Evolution Rate.

A universal approach for enhancing water affinity in polymer photocatalysts by covalently attaching hydrophilic photocrosslinkers to polymer chains is presented. A series of bisdiazirine photocrosslinkers, each comprising bisdiazirine photophores linked by various aliphatic (CL-R) or ethylene glycol-based bridge chains (CL-TEG), is designed to prevent crosslinked polymer photocatalysts from degradation through a safe and efficient photocrosslinking reaction at a wavelength of 365nm. When employing the hydrophilic CL-TEG as a photocrosslinker with polymer photocatalysts (F8BT), the hydrogen evolution reaction (HER) rate is considerably enhanced by 2.5-fold compared to that obtained using non-crosslinked F8BT photocatalysts, whereas CL-R-based photocatalysts yield HER rates comparable to those of non-crosslinked counterparts. Photophysical analyses including time-resolved photoluminescence and transient absorption measurements reveal that adding CL-TEG accelerates exciton separation, forming long-lived charge carriers. Additionally, the in-depth study using molecular dynamics simulations elucidates the dual role of CL-TEG: it enhances water penetration into the polymer matrix and stabilizes charge carriers after exciton generation against undesirable recombination. Therefore, the strategy highlights endowing a high-permittivity environment within polymer photocatalyst in a controlled manner is crucial for enhancing photocatalytic redox reactivity. Furthermore, this study shows that this hydrophilic crosslinker approach has a broad applicability in general polymer semiconductors and their nanoparticulate photocatalysts.

3D-Networks Based Polymer Composites for Multifunctional Thermal Management and Electromagnetic Protection: A Mini Review

The rapid development of miniaturized, high-frequency, and highly integrated microelectronic devices has brought about critical issues in electromagnetic compatibility and thermal management. In recent years, there has been significant interest in lightweight polymer-based composites that offer both electromagnetic interference (EMI) shielding and thermal conductivity. One promising approach involves constructing three-dimensional (3D) interconnection networks using functional fillers in the polymer matrix. These networks have been proven effective in enhancing the thermal and electrical conductivity of the composites. This mini-review focuses on the preparation and properties of 3D network-reinforced polymer composites, specifically those incorporating metal, carbon, ceramic, and hybrid networks. By comparing the effects of different filler types and distribution on the composite materials, the advantages of 3D interconnected conductive networks in polymer composites are highlighted. Additionally, this review addresses the challenges faced in the field of multifunctional thermal management and electromagnetic protection materials and provides insights into future development trends and application prospects of 3D structured composites.

High‐Efficiency Semitransparent Near‐Infrared Organic Photodetectors Enabled by a Molecular Crystal Network

AbstractSemitransparent organic photodetectors (ST‐OPDs) show immense promise for integration into optoelectronic devices, offering adjustable absorption and see‐through functionalities. However, achieving high‐performance ST‐OPDs remains challenging, necessitating a delicate balance of low dark current density, high external quantum efficiency, and optimal visible light transmission. Here, a strategy is presented using anode interfacial materials (AIMs) as the donor and narrow bandgap non‐fullerene acceptors (NFAs) to formulate the donor: acceptor light‐sensitive layer. Critical to the approach is the incorporation of 1,8‐diiodooctane during film processing, enabling the formation of morphology with an NFA molecular crystal network embedded within the donor polymer matrix. This optimized morphology substantially boosted device external quantum efficiency and reduced dark current under reverse bias, yielding a remarkable special detectivity of over 1013 Jones at 840 nm under a bias of −0.1 V. ST‐OPDs are achieved with detectivity surpassing 1012 Jones and notable average visible transmittance of over 50%. These findings highlight the potential of AIM:NFA combinations for high‐efficiency ST‐OPDs by finely controlling morphology through multiple length scales, opening doors for various applications in transparent electronics and beyond.

A new polyazomethine-based pyrazole moiety and its reinforced nanocomposites @ ZnO for antimicrobial applications

ABSTRACT A new class of biologically active polyazomethine/pyrazole and their related nanocomposites, polyazomethine/pyrazole/zinc oxide nanoparticles, have been successfully synthesized through the polycondensation technique in the form of polyazomethine pyrazole (PAZm/Py4–6) and polyazomethine/pyrazole/zinc oxide nanoparticles (PAZm/Py/ZnOa-c). The polymeric nanocomposites were prepared with a 5% loading of zinc oxide nanofiller using the same preparation technique, in addition to the help of ultrasonic radiation. The characteristics of the new polymers, such as solubility, viscometry, and molecular weight, were examined. All the polymers were completely soluble in the following solvents: concentrated sulfuric acid, formic acid, dimethylformamide, dimethyl sulfoxide, and tetrahydrofuran. Furthermore, the weight loss of the polyazomethine pyrazole (4, 5, and 6) at 800 °C was 67%, 95%, and 86%, respectively, which indicates the thermal stability of these polymers. At 800 °C, the polyazomethine/pyrazole/zinc oxide nanoparticles (a, b, and c) lost 74%, 68%, and 75% of their weight, respectively. This shows that adding zinc oxide nanoparticles made these compounds more stable at high temperatures. The X-Ray diffraction pattern of the polyazomethine pyrazole (PAZm/Py4–6) shows a number of sharp peaks with varying intensities. The polymers that were studied had straight crystal structures. Furthermore, the measurements of polyazomethine/pyrazole/zinc oxide nanoparticles (PAZm/Py/ZnOa-c) indicate a good merging of zinc oxide nanoparticles into the matrix of polymers. The antimicrobial activity of polymers and polymer nanocomposites was tested against some selected bacteria and fungi. The synthesized polymer (c) shows the highest activity against the two types of gram-negative bacteria selected. Most tested compounds were found to be effective against gram-positive bacteria except polyazomethine pyrazole (PAZm/Py5) and polyazomethine pyrazole (PAZm/Py6), which do not exhibit any activity. The synthesized polymers and their related nanocomposites were tested for their ability to kill the chosen fungi. All of them were effective against Aspergillus flavus, but only polyazomethine pyrazole (PAZm/Py4) and polyazomethine/pyrazole/zinc oxide (PAZm/Py/ZnOc) were effective against Candida albicans.

Interfacial compatible PolyMOF membranes as ratiometric fluorescence temperature sensors

Cryogenic temperature sensors play significant roles in manufacturing, metallurgy, and aerospace. Metal-organic frameworks (MOFs) as emerging crystal materials exhibited inherent advantages as fluorescence temperature sensors and researchers have shifted their focus toward incorporating MOFs materials into mixed matrix membranes (MMMs) for broader practical applications. However, the poor interfacial compatibility between MOFs particles and the polymer matrix would cause aggregation-induced fluorescence quenching and reduced energy transfer efficiency, thereby compromising temperature sensing performances. Herein, we adopt a post-synthetic copolymerization strategy to realize an interfacial-compatible membranous ratiometric luminescent thermometer based on the emissions of ligands and lanthanide ions. Benefiting from the controllable covalent cross-linking structures, the designed polyMOF membrane exhibited excellent interfacial compatibility and avoided MOFs irregular morphology agglomeration and phase separation, which contributed to outstanding fluorescence temperature sensing performance with excellent sensitivity ranging from 0.300 to 0.745 %·K−1 within the temperature range of 80–300 K, superior to recent reported MOFs-based thermometers. This research presents a promising approach for the design and fabrication of interfacial compatible MOFs-based membranes with excellent fluorescence temperature sensing properties, advancing the understanding of structure-property relationships and accelerating the practical applications.

Synthesis of Hybrid/Superhydrophobic Coupling Agent Grafted Nano SiO2 and Its Use in Fabrication of Rubber Nanocomposite with Outstanding Oil/Water Separation Capability

Design and synthesis of a new sorbent with high performances of oil-water separation is one of the challenges to the world community. Herein, a superhydrophobic/novel coupling agent (NCA) containing several vinyl groups was synthesized. Also, vinyl isocyanate (VI) and tetraethoxysilane (TEOS) reacted with a synergetic strategy of crosslinked networks through the click reaction under N2 gas atmosphere. 1H NMR and FTIR analyses confirmed the formation of NCA with the SiC10H18O6N2 chemical formula. Then, NCA was grafted on the nanoparticles at different amounts by sol-gel method. It was found that the surface modification of nanoparticles enhanced the water contact angle (WCA) from 60° to 163°. In the following, nanoparticles with and without NCA were applied at different contents to tire rubber compound. The uniform dispersion/distribution of the grafted nano fillers with NCA in polymer matrix and the strong filler-polymer interactions enhanced crosslink density and improved the mechanical performances of the rubber sample. The prepared nanocomposites were tested against absorption of different oils. The results showed that the superior nanocomposite with modified nanoparticles (i.e. TR-TNS5) had a separation efficiency of over 90 % compared to the nanocomposite with pure nanoparticles (i.e. TR-NS5) which had a separation efficiency of less than 30 %. Also, the separation cycle of nanocomposites improved by 95 % after addition of the modified nanoparticles (from 240 to 440 cycles). The modified nanocomposite illustrated contact angles of 153.22° and 13.34° with water and oil droplets, respectively. The results showed that the modified rubbery nanocomposite confirmed superior mechanical and oil-water separation performances.

An ambipolar PEDOT-perfluorinated porphyrin electropolymer: application as an active material in energy storage systems.

The development of functional organic materials is crucial for the advancement of various fields, such as optoelectronics, energy storage, sensing, and biomedicine. In this context, we successfully prepared a stable ambipolar perfluoroporphyrin-based polymeric film by electrochemical synthesis. Our strategy involved the synthesis of a novel tetra-pentafluorophenyl porphyrin covalently linked to four 3,4-ethylenedioxythiophene (EDOT) moieties. The resulting monomer, EDOT-TPPF16, was obtained through a straightforward synthetic approach with a good overall yield. The unique molecular structure of EDOT-TPPF16 serves a dual function, with EDOT moieties allowing electropolymerization for polymeric film formation, while the electron-acceptor porphyrin core enables electrochemical reduction and electron transport. The electrochemical polymerization permits the polymer (PEDOT-TPPF16) synthesis and film formation in a reproducible and controllable manner in one step at room temperature. Spectroelectrochemical experiments confirmed that the porphyrin retained its optoelectronic properties within the polymeric matrix after the electrochemical polymerization. The obtained polymeric material exhibited stable redox capabilities. Current charge-discharge cycles and electrochemical impedance spectroscopy of the electrochemically generated organic film demonstrated that the polymer could be applied as a promising active material in the development of supercapacitor energy storage devices.

Influence of synthesis conditions and raw materials on the properties of N‐chlorosulfonamides immobilized on granular styrene–divinylbenzene polymer carriers

AbstractPolymer materials with immobilized functional groups–donors of active chlorine are widely used to create products with a microbiocidal effect and increased resistance to microbial contamination. In this work, various methods for the synthesis of granular styrene–divinylbenzene polymers with N‐chlorosulfonamide groups were investigated. It has been shown that the synthesis of polymers with chlorine‐active SO2NNaCl groups from a non‐functionalized styrene–divinylbenzene polymer matrix through the stage of its sulfochlorination with chlorosulfonic acid in dichloromethane for 6–7 h is optimal. These products contain approximately 11% of active chlorine and maintain a stable particle size distribution. When cation exchangers such as Purolite C100 are used as the initial polymer carrier, the content of chlorine‐active groups in the target product is approximately 9%, and an increase in the content of the dust fraction is observed. The obtained samples, regardless of the synthesis method, are capable of releasing active chlorine into solutions containing amino compounds. The microbial impurities in water also cause the emission of active chlorine in an amount that does not depend on the loading of the polymer, but is determined by the concentration of microbes, due to which a pronounced antimicrobial effect is observed. In this case, the resulting products do not cause further decomposition of the functional groups of the polymer, which indicates the high service life of the latter. The availability of raw materials, relative ease of synthesis, stability, possibility of regeneration and microbiocidal properties of the studied polymers make them promising for use as components of water and air purification systems and other products for medical and industrial purposes. © 2024 Society of Chemical Industry.