Polymer Mixtures Research Articles

UV-assisted robotic arm freeforming of SiOC ceramics from a preceramic polymer

Material extrusion is a very common and facile additive manufacturing technique for ceramic materials, allowing for rapid design and fabrication of 3D structures without expensive tools. However, fabricating sophisticated structures with large spanning parts and overhanging features using this technology is still a challenge. Here, UV-assisted additive manufacturing is enabled by performing material extrusion with the assistance of UV light using mixture of a preceramic polymer and a photopolymer. The rheological properties of the ink were investigated under UV light radiation to optimize the printing parameters to achieve excellent printability. Complex ceramic structures were fabricated with this method, such as spiral and truss structures, which would be very difficult to obtain using traditional material extrusion without sacrificial supports. These structures have potential application in lightweight ceramic components, such as sandwich structures.

Online coupling of liquid chromatography and two-dimensional diffusion ordered spectroscopy for the analysis of oligostyrenes

The aim of this study was to introduce a powerful coupling of Liquid Adsorption Chromatography (LAC) and Diffusion-Ordered Spectroscopy (DOSY) for comprehensive structure analysis. This new hyphenation approach facilitated the simultaneous separation of a polymer mixture and the determination of molar masses within a single 3D experiment. The online coupling of High-Performance Liquid Chromatography (HPLC) and two-dimensional DOSY-NMR will be called 3D-LAC-NMR-DOSY experiment. Our methodology enabled the chromatographic separation of analytes based on their chemical heterogeneity, and provided accurate molar masses of the analytes through 2D-DOSY. This new method was demonstrated on a polystyrene oligomer mixture. In this case, the oligostyrenes could be separated with LAC according to their tacticity and chain length in protonated acetonitrile as eluent and DOSY measurements provided the molar masses of each oligomer. In order to show the power of the 3D-LAC-NMR-DOSY method, the comparison to 2D-DOSY, 3D-DOSY and LAC-NMR was separately evaluated. Furthermore, the recently published solvent-independent molar mass calibration of diffusion coefficients was also successfully applied in our LAC-DOSY studies for molar mass predictions of the oligomers in acetonitrile. The predicted molar masses were in good agreement with the LAC-DOSY measurements and were verified by calibrations of diffusion coefficients and mass spectrometry. Finally, this pioneering 3D technique offers a powerful new tool for advancing structure analysis and enhancing our understanding of complex systems such as oligostyrenes.

Spatially Resolved Anisotropic Natural Abundance Deuterium 2D-NMR Spectroscopy Using Bimesophasic Lyotropic Chiral Systems.

In this paper, we describe, for the first time, the combined and original use of spatially resolved anisotropic natural abundance deuterium (ANAD) 2D-NMR experiments and bimesophasic lyotropic chiral systems to extract two independent sets of anisotropic parameters such as 2H-RQCs from a single NMR sample. As a pioneering example, we focus on a mixture of immiscible polypeptides (PBLG) and polyacetylene helical polymers (L-MSP) dissolved in weakly polar organic solvents (chloroform). Nondeuterated (D)-(+)-camphor is used as a model chiral solute. By providing two series of 2H-RQCs, this new analytical approach paves the way for applications in 3D structure elucidation with increased reliability and also opens up original investigations in terms of spectral enantiomeric discriminations and mixing of helical polymers.

Leaching of catalyst platinum from cured silicone elastomers: A preliminary study for comparing reagents

Addition curing systems involve two-part silicones which require the mixture of a silicone polymer with a catalyst to initiate the cure. Platinum is the most commonly used metal catalyst for addition curing of silicones by hydrosilylation which involves the crosslinking by the addition reaction of silicon hydride species to unsaturated bonds, mainly CC, but also CO or CN double bonds. After crosslinking of the polymers, the platinum catalyst cannot be recovered but remains in the silicone materials throughout the entire product life. In the end, platinum is disposed of together with the silicones and is thus lost to the value chain. The overall objective of this work was to develop a recycling process for the recovery of platinum from addition-cured silicone elastomers. In the first step, this was achieved by efficient digestion methods and by optimizing the leaching processes for exemplary commercial silicone elastomer products. Two different silicone materials were investigated, both of which were crosslinked with a platinum catalyst. The initial Pt content in the tested samples was 12.6 ± 0.2 mg/kg for a commercial silicone impression material and 6.3 ± 0.5 mg/kg for a silicone baking mold, measured by graphite furnace atomic absorption spectrometry (GF-AAS). Samples were first frozen with liquid nitrogen to improve brittleness and then crushed with a simple food processor to obtain a silicone granule. Various acid mixtures, mainly based on sulfuric acid, were investigated as digestion methods in order to extract platinum from the silicone network. These had different effects on the dissolution behavior of silicone samples and the amount of platinum extracted in each case. The amount of platinum leached from the filtrate of the digested samples in each case was measured by ICP-OES to evaluate the efficiency of different leaching mixtures. In addition, the dissolved platinum species present in the solutions was identified by UV/VIS as tetrachloridoplatinate(II) complex. The best platinum leaching results so far were obtained with two methods, both of which used a leaching mixture based on sulfuric acid and hexamethyldisiloxane (M2). In the presence of hydrochloric acid, 9.6 ± 1.6 mg platinum/kg was leached from the silicone impression material and 4.2 ± 0.8 mg platinum/kg from the silicone baking mold. With the additional use of aqua regia instead of hydrochloric acid, 10.4 ± 2.8 mg platinum/kg was extracted from the silicone impression material and 4.8 ± 1.0 mg platinum/kg was extracted from the silicone baking mold. These methods were replicated with n = 3. Using statistical evaluation methods (F-test, t-test, and confidence interval), no significant difference was found between these two best methods. Recovery of platinum(0) from leach mixtures has not yet been achieved due to high dilution and very low platinum concentration in samples and will be part of another study.

Influence of chloride salt erosion on the adhesion of asphalt-aggregate interfaces considering mineral anisotropy: insights from molecular dynamics.

Asphalt, a polymer mixture composed of various hydrocarbons, is extensively utilized due to its excellent performance. To evaluate the sensitivity of asphalt concrete to chloride salt damage at the nanoscale, considering the anisotropy of aggregate mineral crystal orientation, molecular dynamic simulations were employed to model the interface interactions between asphalt and aggregate mineral components (silica and calcite) under chloride salt exposure. The wetting processes of water droplets and chloride salt droplets on different crystal surfaces of silica and calcite were analyzed. Furthermore, the adhesive energy, decohesion energy, degradation ratio, and energy ratio of the interaction model between asphalt and aggregate mineral interfaces were analyzed to reveal the variations in the interfaces between the two components. The results demonstrated that the anisotropy of the minerals significantly affects the adhesion energy of asphalt and aggregate. Moreover, the surface hydrophilicity of calcite was larger than that of silica. The interfacial adhesion energy of asphalt-calcite was larger than that of asphalt-silica under dry condition and chloride salt attack, and the interfacial adhesion energy of both asphalt and mineral decreased with the increase of chloride salt concentration. The degradation ratio and energy ratio values of asphalt and calcite were larger than those of asphalt and silica, and the anisotropy of the mineral surface affected the degradation ratio and energy ratio values. This study provides a new method and theoretical basis for further research on the damage mechanism and strengthening measures of asphalt-aggregate under chloride salt attack. To investigate the interaction between asphalt and mineral aggregates under chloride salt erosion, models of asphalt, aggregate, and asphalt/aggregate composite systems were constructed using the Amorphous Cell module in Materials Studio 2020 software. Molecular dynamic simulations of the asphalt/aggregate composite system were then conducted using the Forcite module, employing the COMPASS II force field to describe atomic and molecular interactions. Initially, considering the crystal orientation and surface configuration of the aggregate minerals, the impact of mineral anisotropy on the asphalt-aggregate interface model was analyzed. Subsequently, by simulating the contact states of nano water droplets and chloride salt droplets with different mineral surfaces, the wetting characteristics of nano water droplets on silica and calcite surfaces were determined. Lastly, considering the corrosion effect of chloride solution at different concentrations, the adhesion energy, debonding energy, degradation ratio, and energy ratio of the asphalt-aggregate interface interaction model were analyzed.

Wharton's jelly-derived multifunctional hydrogels: New tools to promote intervertebral disc regeneration in vitro and ex vivo.

The degeneration of intervertebral disc (IVD) is a disease of the entire joint between two vertebrae in the spine caused by loss of extracellular matrix (ECM) integrity, to date with no cure. The various regenerative approaches proposed so far have led to very limited successes. An emerging opportunity arises from the use of decellularized ECM as a scaffolding material that, directly or in combination with other materials, has greatly facilitated the advancement of tissue engineering. Here we focused on the decellularized matrix obtained from human umbilical cord Wharton's jelly (DWJ) which retains several structural and bioactive molecules very similar to those of the IVD ECM. However, being a viscous gel, DWJ has limited ability to retain ordered structural features when considered as architecture scaffold. To overcome this limitation, we produced DWJ-based multifunctional hydrogels, in the form of 3D millicylinders containing different percentages of alginate, a seaweed-derived polysaccharide, and gelatin, denatured collagen, which may impart mechanical integrity to the biologically active DWJ. The developed protocol, based on a freezing step, leads to the consolidation of the entire polymeric dispersion mixture, followed by an ionic gelation step and a freeze-drying process. Finally, a porous, stable, easily storable, and suitable matrix for ex vivo experiments was obtained. The properties of the millicylinders (Wharton's jelly millicylinders [WJMs]) were then tested in culture of degenerated IVD cells isolated from disc tissues of patients undergoing surgical discectomy. We found that WJMs with the highest percentage of DWJ were effective in supporting cell migration, restoration of the IVD phenotype (increased expression of Collagen type 2, aggrecan, Sox9 and FOXO3a), anti-inflammatory action, and stem cell activity of resident progenitor/notochordal cells (increased number of CD24 positive cells). We are confident that the DWJ-based formulations proposed here can provide adequate stimuli to the cells present in the degenerated IVD to restart the anabolic machinery.

Molecular Interaction Study in the Binary Liquid Mixture of PEO and DMF by Ultrasonic Technique

The non‐destructive ultrasonic technique is a great employ for knowing the solute–solvent interaction in the polymer blend. By the ultrasonic velocity and attenuation evaluation, the visco‐elastic behaviors of the polymer solution have been assessed and compared with the results of conventional dynamic mechanical analysis. In the present research work, a comprehensive ultrasonic investigation of molecular interaction in a polymeric mixture of Poly (ethylene oxide) PEO and dimethyformamide (DMF) at 333 K has been executed by using the information provided by the literature. For this purpose, ultrasonic waves of two different frequencies such as 2 and 5 MHz have been implemented. Several acoustical parameters such as adiabatic compressibility, acoustic impedance, relaxation time, and ultrasonic attenuation coefficient (𝛼/𝑓2) are explored. Thermodynamic parameters like relative association and intermolecular free path length are also estimated. The evaluated values have been associated with the previous experimental results. The non‐ideal approach of the solution is analyzed and discussed in detail.

VARIATION IN THERMAL STRESS BEHAVIOUR OF COMPOSITE MATERIALS BY THERMOMECHANICAL TECHNIQUE (TMA)

In this study, a polymeric-based composite material was made using 80% epoxy polyester 20% and unsaturated polyester resin. The polymeric composites were prepared by manual moulding method by adding a support material of silica powder to the mixture by weight (0%, 5%, 10%, and 15%) to examine one of the thermal properties which are thermal expansion. A comparison was made with the polymeric mixture before and after the reinforcement. The results of the study showed that the coefficient of thermal expansion increases with increasing temperatures, while it decreases at high temperatures. The results also showed that there is a decrease in the degree of glass transition with an increase in the concentration of the additive, and it was also noted that an increase in the percentage of silica at 15% decreases the value of the thermal expansion coefficient compared to other samples.

Laboratory evaluation of high-temperature resistant lysine-based polymer Gel systems for leakage control

In-situ crosslinking gel known for its cost-effectiveness, has been employed for decades to plug high-permeability features in subsurface environments. However, some commonly used crosslinkers are being phased out due to the increasingly rigorous environmental regulations. As a newly discovered environmentally friendly crosslinker, lysine can crosslink the partially hydrolyzed polyacrylamide through transamidation reaction. The present work aimed to study the effect of polymer composition and concentration on the gelation behavior of lysine and high molecular weight acrylamide-based polymers. Several commercial high molecular weight polymers with different contents of 2-Acrylamido-2-methyl-1-propane sulfonic acid (AMPS) including AN-105/125, SAV-55/37/28, and SAV-10 were deployed in this work. High-temperature/pressure-resistant glass tubes were used to study the crosslinking behavior. The plugging efficiency test used a high permeability sandstone core (1600 mD). Besides, the effect of salinity and pH on the crosslinking behavior, gel strength, and long-term thermal stability was also studied. Results showed that increasing the AMPS content could prolong the gelation time, but the polymer and lysine mixture failed to form gels when the AMPS content was excessively high. Additionally, increasing the AMPS content negatively affects the gel strength but positively impacts long-term thermal stability. Polymer gel with a relatively high content of AMPS could be stable in 0.5 % CaCl2 solution at 130 °C for over 200 days. The polymer/lysine gel system can efficiently plug the high permeability matrix, and the plugging efficiency is higher than 99 %. The polymer/lysine gel system is a promising green leakage control system in treating the high conductivity features in geothermal and oil reservoirs.

Thermodynamics of the Glassy Polymer State: Equilibrium and Non-Equilibrium Aspects.

This work examines, first, the non-equilibrium character of the glassy state of polymer systems and its significance in the development of novel materials for important technological applications. Subsequently, it summarizes the essentials of the generalized lattice fluid approach for the description of this highly complex non-equilibrium behavior with an approximate and simple, yet analytically powerful formalism. The working equations are derived in a straightforward and consistent manner by clearly defining the universal and specific variables needed to describe the discussed properties. The role of the non-random distribution of molecular species and free volume in the glassy system is also examined, as is the role of strong specific interactions, such as hydrogen-bonding networks. This work also reports examples of applications in a variety of representative systems, including glass densification, retrograde vitrification, increase in glass-transition temperature in hydrogen-bonded polymer mixtures, and hysteresis phenomena in sorption-desorption from glassy polymer matrices.

A Bilayer Microarray Patch (MAP) for HIV Pre-Exposure Prophylaxis: The Role of MAP Designs and Formulation Composition in Enhancing Long-Acting Drug Delivery.

Microarray patches (MAPs) have shown great potential for efficient and patient-friendly drug delivery through the skin; however, improving their delivery efficiency for long-acting drug release remains a significant challenge. This research provides an overview of novel strategies aimed at enhancing the efficiency of MAP delivery of micronized cabotegravir sodium (CAB Na) for HIV pre-exposure prophylaxis (PrEP). The refinement of microneedle design parameters, including needle length, shape, density, and arrangement, and the formulation properties, such as solubility, viscosity, polymer molecular weight, and stability, are crucial for improving penetration and release profiles. Additionally, a bilayer MAP optimization step was conducted by diluting the CAB Na polymeric mixture to localize the drug into the tips of the needles to enable rapid drug deposition into the skin following MAP application. Six MAP designs were analyzed and investigated with regard to delivery efficiency into the skin in ex vivo and in vivo studies. The improved MAP design and formulations were found to be robust and had more than 30% in vivo delivery efficiency, with plasma levels several-fold above the therapeutic concentration over a month. Repeated weekly dosing demonstrated the robustness of MAPs in delivering a consistent and sustained dose of CAB. In summary, CAB Na MAPs were able to deliver therapeutically relevant levels of drug.

Resolving acne with optimized adapalene microspongeal gel, in vivo and clinical evaluations

In our pursuit of enhancing acne treatment while minimizing side effects, we developed tailored Adapalene microsponges (MS) optimized using a Box–Behnken design 33. The independent variables, Eudragit RS100 percentage in the polymer mixture, organic phase volume, and drug to polymer percentage, were explored. The optimized formulation exhibited remarkable characteristics, with a 98.3% ± 1.6 production yield, 97.3% ± 1.64 entrapment efficiency, and a particle size of 31.8 ± 1.1 µm. Notably, it achieved a 24 h cumulative drug release of 75.1% ± 1.4. To delve deeper into its efficacy, we evaluated the optimized microspongeal-gel in vitro, in vivo, and clinically. It demonstrated impressive retention in the pilosebaceous unit, a target for acne treatment. Comparative studies between our optimized Adapalene microspongeal gel and marketed Adapalene revealed superior performance. In vivo studies on Propionibacterium acnes-infected mice ears showed a remarkable 97% reduction in ear thickness, accompanied by a significant decrease in inflammatory signs and NF-κB levels, as confirmed by histopathological and histochemical examination. Moreover, in preliminary clinical evaluation, it demonstrated outstanding effectiveness in reducing comedonal lesions while causing fewer irritations. This not only indicates its potential for clinical application but also underscores its ability to enhance patient satisfaction, paving the way for future commercialization.

Synthesis of a novel clay/polyacrylic acid-tannic acid hydrogel composite for efficient removal of crystal violet dye with low swelling and high adsorption performance

Hydrogels are versatile materials with numerous applications; however, their potential in water treatment is hindered by their tendency to exhibit high swelling, degradation, and excessive water absorption. In this study, a hydrogel composed of natural clay, polyacrylic acid (PAA), and tannic acid (TA) was prepared with varying ratios of TA to control swelling ratio, reduce degradation and enhance adsorption efficiency for removal of cationic dye-contaminated wastewater. The effect of the TA ratio on the physical, chemical, and adsorption properties of prepared hydrogel (clay/PAA-TA) was studied by preparing a series of hydrogel composites and characterizing them using various techniques. The swelling ratio of pure PAA hydrogels was 7061%, but by incorporating TA into the polymer mixture, the swelling ratio decreased to less than 500%, with the lowest observed swelling of 250% occurring at a 5% tannic acid. In adsorption studies, the target pollutant was crystal violet dye (CV) and the pH effect, time effect, temperature and initial dye concentration for the adsorption CV dye were investigated using batch adsorption parameters. Adsorption studies showed that using 5% of TA is the optimal ratio to achieve the highest adsorption capacity of the prepared clay/PAA-TA to uptake CV dye. With an adsorption capacity of 444.5 mg/g, the Langmuir-Freundlich model suited the adsorption isotherm. The adsorption kinetics were best explained by the pseudo-first-order model. The results of thermodynamic studies indicated that the adsorption was spontaneous, favorable, and endothermic.

Protein-Rich Rafts in Hybrid Polymer/Lipid Giant Unilamellar Vesicles.

Considerable attention has been dedicated to lipid rafts due to their importance in numerous cell functions such as membrane trafficking, polarization, and signaling. Next to studies in living cells, artificial micrometer-sized vesicles with a minimal set of components are established as a major tool to understand the phase separation dynamics and their intimate interplay with membrane proteins. In parallel, mixtures of phospholipids and certain amphiphilic polymers simultaneously offer an interface for proteins and mimic this segregation behavior, presenting a tangible synthetic alternative for fundamental studies and bottom-up design of cellular mimics. However, the simultaneous insertion of complex and sensitive membrane proteins is experimentally challenging and thus far has been largely limited to natural lipids. Here, we present the co-reconstitution of the proton pump bo3 oxidase and the proton consumer ATP synthase in hybrid polymer/lipid giant unilamellar vesicles (GUVs) via fusion/electroformation. Variations of the current method allow for tailored reconstitution protocols and control of the vesicle size. In particular, mixing of protein-free and protein-functionalized nanosized vesicles in the electroformation film results in larger GUVs, while separate reconstitution of the respiratory enzymes enables higher ATP synthesis rates. Furthermore, protein labeling provides a synthetic mechanism for phase separation and protein sequestration, mimicking lipid- and protein-mediated domain formation in nature. The latter means opens further possibilities for re-enacting phenomena like supercomplex assembly or symmetry breaking and enriches the toolbox of bottom-up synthetic biology.

Flexible Coatings Facilitate pH-Targeted Drug Release via Self-Unfolding Foils: Applications for Oral Drug Delivery.

Ingestible self-configurable proximity-enabling devices have been developed as a non-invasive platform to improve the bioavailability of drug compounds via swellable or self-unfolding devices. Self-unfolding foils support unidirectional drug release in close proximity to the intestinal epithelium, the main drug absorption site following oral administration. The foils are loaded with a solid-state formulation containing the active pharmaceutical ingredient and then coated and rolled into enteric capsules. The coated lid must remain intact to ensure drug protection in the rolled state until targeted release in the small intestine after capsule disintegration. Despite promising results in previous studies, the deposition of an enteric top coating that remains intact after rolling is still challenging. In this study, we compare different mixtures of enteric polymers and a plasticizer, PEG 6000, as potential coating materials. We evaluate mechanical properties as well as drug protection and targeted release in gastric and intestinal media, respectively. Commercially available Eudragit® FL30D-55 appears to be the most suitable material due to its high strain at failure and integrity after capsule fitting. In vitro studies of coated foils in gastric and intestinal media confirm successful pH-triggered drug release. This indicates the potential advantage of the selected material in the development of self-unfolding foils for oral drug delivery.

Mechanical Properties of PMMA and PLA Modified Epoxy Resins

Last years research in polymers registered an increase of interest regarding polymer mixtures aiming to obtain materials with properties of the mixed polymers. In this respect many studies are pointing the mixtures between a thermoset polymer and a thermoplastic polymer. It is known the fact that thermoplastic polymers are much more malleable than the thermoset ones and the goal is to obtain a mixture with the general properties of the thermoset polymer and with a machining ability proper to the thermoset polymer. The vitrimers are this type of polymers and, some of them, can be obtained by mixing polymers form the two categories. This study is about using solutions of two thermoset polymers to modify the basic properties of three epoxy resins. The results show that the presence of PMMA, respectively, PLA inside the epoxy resin matrix determines changes of the mechanical properties of the formed materials. Without analysing the adhesive properties of new materials is hard to decide about their value from the composites applications point of view.

Thermal and optical properties of P3HT:PC70BM:ZnO nanoparticles composite films

The results of studies on the influence of zinc oxide nanoparticles (ZnO-NPs) on the structural, thermal and optical properties of thin films of mixtures of phenyl-C71-butyric acid methyl ester (PCBM) with poly[3-hexylthiophene] (P3HT) of various molecular weights are described in this article. The structural properties of the layers of: polymers, mixtures of polymers with fullerenes and their composites with ZnO-NPs were investigated using X-ray diffraction. Whereas their glass transition temperature and optical parameters have been determined by temperature-dependent spectroscopic ellipsometry. The presence of ZnO-NPs was also visible in the images of the surface of the composite layers obtained using scanning electron microscopy. These blends and composite films have also been used as the active layer in bulk heterojunction photovoltaic structures. The molecular weight of P3HT (Mw = 65.2; 54.2 and 34.1 kDa) and the addition of nanoparticles affected the power conversion efficiency (PCE) of the obtained solar cells. The determined PCE was the highest for the device prepared from the blend of P3HT:PCBM with the polymer of the lowest molecular weight. However, solar cells with ZnO-NPs present in their active layer had lower efficiency, although the open-circuit voltage and fill factor of almost all devices had the same values whether they contained ZnO-NPs or not. It is worth noting that thermal studies carried out using temperature-dependent ellipsometry showed a significant effect of the presence of ZnO-NPs on the value of the glass transition temperature, which was higher for composite films than for films made of a polymer-fullerene blend alone.

Highly selective solid-liquid extraction of microplastic mixtures as a pre-preparation tool for quantitative nuclear magnetic resonance spectroscopy studies.

Despite various developments in the application of quantitative nuclear magnetic resonance (qNMR) spectroscopy toward microplastics in recent years, this method still lacks suitable sample preparation and fractionation procedures. As this poses a crucial obstacle for its utilisation on environmental samples, which contain various mixtures of polymers along with other matrix substances, this research aims to address this missing link by presenting an easy-to-apply procedure based on common laboratory equipment. The process selectively separates microplastics from inorganic constituents while performing the necessary fractionation of different types of microplastics prior to qNMR analysis. It allows subsequent quantification of polystyrene (PS), polybutadiene rubber (BR), polymethylmethacrylate (PMMA), polyvinylchloride (PVC), polyethylene terephthalate (PET) and polyamide (PA) from a single sample, establishing recovery rates greater than 88% for all tested polymer types. Additionally, we extended our previous qNMR protocol to include two common polymer types: polymethylmethacrylate (PMMA) and polyacrylonitrile (PAN), achieving limits of detection down to 1.76 μg ml-1 and 12.53 μg ml-1 as well as limits of quantification down to 5.88 μg ml-1 and 41.78 μg ml-1, respectively. Thus, the qNMR method presented herein is now applicable to eight abundant polymer types, allowing the quantification of up to three different types simultaneously.

Study of the environmental impact of the process of recycling fibrous waste

The paper considers the formation of composites based on mixtures of powders of highly dispersed polyethylene, polystyrene, natural silk and wool, cellulose, which have good physical and mechanical properties and are suitable for using materials with desired properties. The paper also provides information about composites, the principles of creating polymer composite materials. The main technological methods for obtaining composite materials and methods for molding products based on them are given. It contains data on the features of the structure and properties of the obtained polymer composites: particulate-filled, fiberreinforced, polymer mixtures. The study's findings also show that the creation of new technological procedures will enable the optimization of waste's resource potential, the reduction of waste sent for disposal to lessen waste's detrimental effects on the environment, and the expansion of the range of materials available for use in household, technical, and special applications. The parameters of the greatest technologies currently in use are suggested, together with technological, technical, and administrative solutions for waste processing.

Poly (ether sulfone) (PES)/polystyrene (PS) Thermoplastic Polymer Blend: Molecular Dynamics (MD) Simulation Methods and Experimental to Miscibility Evaluation

In this study, poly (ether sulfone) (PES)/polystyrene (PS) thermoplastic polymer blend miscibility was looked at using both molecular dynamics (MD) simulations and experiments. In particular, the parameters of the Flory-Huggins interaction and the heat of mixing of poly (ether sulfone) (PES)/polystyrene (PS) blends at different compositions were calculated from MD simulation. For the PES/PS blend, both differential scanning calorimetry (DSC) and MD simulation showed that they are immiscible at PES/PS: 80/20,60/40 ratios. The degree of compatibility of the 20/80 and 40/60 PES/PS blends is higher than that of a PES-rich blend. This thermodynamic behavior was found to be due mainly to intermolecular interactions. Scanning electron microscopy (SEM) results confirmed this observation. Results show that the calculated and#120594; value is positive at the compositions of PES/PS: 80/20 and 60/40, which confirmed that the polymer mixtures were immiscible at these compositions. The miscibility between PES and PS at these ratios is attributed to favorable van der Waals interactions. Also, the results of the DREIDING 2.21 force field show that electrostatic energy, bond angle bending energy, and bond stretching energy may be to blame for the immiscibility of certain composition polymer blends (PES/PS: 80/20 and 60/40).