Search Results (189)

Background: Previous research has demonstrated that 20 kHz probe or 37 kHz bath sonication of poloxamers comprising polypropylene glycol (PPG) and polyethylene glycol (PEG) blocks can generate degradation byproducts that are toxic to mammalian cells and organisms. Herein, an investigation of a PEGylated phospholipid micelle was undertaken to identify low-molecular-weight sonolytic degradation byproducts that could be cytotoxic. The concern here lies with the fact that sonication is a frequently employed step in drug delivery manufacturing processes, during which PEGylated phospholipids can be subjected to shear forces and other extreme oxidative and thermal conditions. Methods: Control and 20 kHz-sonicated micelles of DSPE-mPEG2000 were analyzed using dynamic light scattering (DLS) and zeta potential analyses to study colloidal properties, matrix-assisted laser desorption/ionization–time of flight (MALDI-TOF) mass spectroscopy (MS) and proton nuclear magnetic resonance (¹H-NMR) spectroscopy to study the structural integrity of DSPE-mPEG2000, and ¹H-NMR spectroscopy and high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection to quantitate the formation of low-molecular-weight degradation byproducts. Results: MALDI-TOF-MS analyses of 20 kHz-sonicated DSPE-mPEG2000 revealed the loss of ethylene glycol moieties in accordance with depolymerization of the PEG chain; ¹H-NMR spectroscopy showed the presence of formate, a known oxidative/thermal degradation product of PEG; and HPLC-UV showed that the generation of formate was dependent on 20 kHz probe sonication time between 5 and 60 min. Conclusions: It was found that 20 kHz sonication can degrade the PEG chain of DSPE-mPEG2000, altering the micelle’s PEG corona and generating formate, a known ocular toxicant. Full article

In response to growing global concerns about plastic waste, the development of efficient recycling technologies for thermoplastics has become increasingly important. Polypropylene (PP), a widely used commodity resin, is of particular interest because of the urgent need to establish sustainable material circulation. However, conventional mechanical property evaluations of injection-molded products typically require dedicated specimens, which involve additional material and energy costs. As described herein, we propose a simplified mechanical model to derive Poisson’s ratio and critical expansion stress directly from standard uniaxial tensile tests of molded thermoplastics. The method based on the true stress–true strain relationship in the small deformation region was validated using various thermoplastics (PP, POM, PC, and ABS), with results showing good agreement with those of the existing literature. The model was applied further to assess changes in mechanical properties of Homo-PP and Block-PP subjected to repeated extrusion. Both materials exhibited reductions in elastic modulus and critical expansion stress with increasing extrusion cycles, whereas Block-PP showed a slower degradation rate because of thermo-crosslinking in its ethylene–propylene rubber (EPR) phase. DSC and chemiluminescence analyses suggested changes in stereoregularity and radical formation as key factors. This method offers a practical approach for evaluating recycled PP and contributes to high-quality recycling and material design. Full article

The growing demand for direct current transmission emphasizes the need for advanced insulation suitable for high-capacity, long-distance applications. Thermoplastics, especially polypropylene, offer several advantages over conventional materials like XLPE (cross-linked polyethylene) and EPR (ethylene propylene rubber), including higher thermal stability, recyclability, and reduced space charge accumulation. However, due to the inherent rigidity and limited flexibility of PP, its mechanical aging becomes a critical factor in assessing its long-term reliability as a cable insulation. In this study, mechanical aging characteristics, specifically declines in tensile strength and elongation, were selected as key indicators of insulation aging. Accelerated aging tests were conducted at 90 °C, 110 °C, and 130 °C for up to 5000 h. The experimental data were fitted to exponential models to derive aging coefficients, which formed the basis for the proposed aging model and the ACI (aging condition index). The ACI enables quantitative assessment of the current insulation condition and estimation of the remaining lifetime until a predefined threshold (e.g., ACI = 0.5) is reached. These findings contribute to the development of condition-based maintenance strategies and long-term asset management for power cables, offering practical insights for improving the reliability of future power grid systems. Full article

The high-temperature performance of well cement is critical for the construction of deep geothermal wells and high-temperature energy storage wells, where mechanical integrity and pore structure stability govern wellbore reliability. To address the strength degradation and structural deterioration of conventional cements under high temperature, the G-class cement was modified by ethylene-vinyl acetate (EVA) polymer and polypropylene fibers (PF), and their impact under various temperatures was explored. Results show that at 600 °C, the compressive strength of modified cement remains above 30 MPa. While the cumulative pore area decreases at 500 °C, a significant increase in larger pores and a major restructuring of the pore network occurs at 600 °C, reflecting the dual effects of high temperature on the pore structure. The modified cement retains structural integrity and excellent mechanical performance up to 400 °C with minimal strength loss, uniform strain distribution, and stable pore structure. At 500 °C and above, it still maintains load-bearing capacity and deformation adaptability, meeting the service requirements for geothermal wells and high-temperature energy storage wells. Even at 600 °C, the reinforcing effect of EVA and PF degradation products slow down crack propagation, ensuring durability in extreme conditions. The research findings lay the foundation for the development of well cement for high-temperature service environments. Full article

Reducing the environmental impact is a key reason for developing recyclable insulation materials for high-voltage industries. In this study, polypropylene (PP) blends were prepared via melt mixing with styrene–ethylene–butylene–styrene (SEBS), a thermoplastic elastomer, to improve breakdown strengths at various cooling speeds. A systematic investigation was conducted to evaluate the influence of crystal size, degree of crystallinity, and nucleation growth rate on the breakdown strength. Crystallization behavior was analyzed using isothermal and non-isothermal methods based on the Avrami model. Increasing SEBS content reduced crystallinity, with the lowest nucleation growth rate observed at 35% SEBS. Breakdown strength correlated with crystallization behavior and was further validated by Weibull distribution method. Notably, PP/SEBS blends containing 35% SEBS exhibited the highest breakdown strength of 66.4 kV/mm at a cooling speed of 10 °C/mm. This improvement reflected a reduction in the degree of crystallinity from 36.0% to 22.9% and the lowest growth rate constant (k) at 35% SEBS. Furthermore, the predicted lifetime of PP/SEBS blend containing 35% SEBS, calculated using the oxidation induction time and the Arrhenius equation, was 42 years. These findings demonstrate that SEBS content and cooling rate effectively modulate crystallization and breakdown strength, enabling recyclable PP/SEBS with XLPE-comparable performance for sustainable high-voltage insulation. Full article

This study aimed to (i) characterize municipal solid waste (MSW) sourced from Utah and Michigan transfer stations and (ii) upcycle, produce, and evaluate composites derived from this MSW. Composition analysis showed that the MSW was composed of a variety of commodity plastics, paper/cardboard, and inorganic materials. Detailed chemical analysis for lignin, cellulose, hemicellulose, and lipids was performed. The plastics identified were mainly polyethylene, polypropylene, polystyrene, and poly (ethylene terephthalate). The compoundability of the MSW was assessed by torque rheometry. Composites were prepared by compounding the MSW in an extruder. A composite flexural strength of 29 MPa and a modulus of 1.0 GPa was achieved. The thermal properties of the composites were also determined. The melt flow behavior of the MSW composites at 190 °C was comparable to wood plastic composite formulations. Full article

To enhance the dispersion of silica within a natural rubber (NR) matrix and improve the modification efficiency of the silane coupling agent, a novel interfacial dispersant composed of block polyether with a PEO-PPO-PEO structure is employed in this study. This block polyether, consisting of poly(ethylene oxide) (PEO) and poly(propylene oxide) (PPO), serves to reduce the surface energy of silica and improve its compatibility with the rubber matrix. Three types of block polyethers with different hydrophilic–lipophilic balance (HLB) values of 8, 13, and 22 are selected to regulate the surface tension of silica. Subsequently, bis[γ-(triethoxysilyl)propyl] tetrasulfide (TESPT) is used to further modify the silica surface, aiming to prepare high-performance rubber composites. The results indicate that the HLB value of the block polyether has a significant influence on the system. Compared with block polyethers having HLB values of 8 and 22, the block polyether with an HLB value of 13 demonstrated superior silica dispersion, leading to enhanced filler–rubber interfacial interactions. Consequently, both the mechanical properties and processability of the NR composites were substantially improved. When the dosage of this block polyether was 1 phr, the composite exhibited a tensile strength of 28.9 MPa and an elongation at break of 523%. Full article

The properties of compatibilized blends of polyethylene (PE) and polypropylene (PP), having reduced macromolecular entanglements, were studied. The density of PP macromolecular entanglements was controlled by prior disentangling in solution. The polymer ratio in the blend was 4:1 or 1:4. An ethylene–octene copolymer was used as a compatibilizer. The melt blending process resulted in good dispersion of the minority component, with slightly larger inclusions when more disentangled PP was used. Rheological studies confirmed the achievement of different entanglement densities of PP macromolecules in the blends. The partial disentanglement did not affect the thermal stability of the blends. During the isothermal crystallization studies, faster growth of PP spherulites was observed in the blend with reduced entanglements, which also influenced the entire crystallization process. The recovery time of equilibrium entanglement was investigated and it turned out to be 45 min if the blend was annealed at 190 °C, which was shorter than in the analogous homopolymer. Studies of tensile properties showed that in blends with a majority share of polyethylene, the elongation at break increased with the disentanglement of the minority component, due to better bonding of the blend components and thus the reduction in microcavitation. Full article

Microplastics (MPs) in agricultural soils pose risks to human health in their potential accumulation along the food chain, and their characteristics require further understanding to implement targeted measures. This study investigated the MP characteristics in typical mulching soils from different farming scales in Sichuan Province, which is one of China’s key agricultural regions, and it also innovatively measured the ecological risk by incorporating size into assessments. The investigated sites showed average microplastic abundances of 19696.81 ± 13226.89, and these were dominated by small-sized ethylene–propylene copolymer (E/P), polypropylene (PP), and polyethylene (PE) particles in yellow-to-brown and black-to-shallow-gray soil. Size-considered evaluation suggested that most of the sites were at a high level of risk. It was found that microplastic pollution varies with farming scales. Larger-scale farming sites primarily received MPs from plastic mulching, while smaller-scale sites were likely affected by a range of non-agricultural sources. The risk assessment showed significant contributions from polyamide (PA) and polyphenylene sulfide (PPS). These results indicate that environmental management strategies should tailor source control measures according to agricultural scales and prioritize high-risk polymers, as well as that MP risk evaluations should include “size” along with “pollution load” and “chemical composition” to better reflect the impact of MPs on ecosystems. Full article

The co-occurrence of microplastics (MPs) and antibiotics as emerging contaminants demonstrates significant ecological perturbations in soil matrices. Of particular scientific interest is the potential for MPs to mediate the environmental fate and transport dynamics of co-existing antibiotics. This study investigated MP-mediated ciprofloxacin (CIP) adsorption in lateritic soils. Batch experiments with polyethylene (PE), polypropylene (PP), and poly (ethylene-terephthalate) (PET) revealed soil components dominated CIP retention, while 10% (w/w) MPs reduced soil adsorption capacity by ≥10.8%, with inhibition intensity following PET > PE > PP. Adsorption thermodynamics exhibited significant pH dependence, achieving maximum sorption efficiency at pH 5.0 (± 0.2), which was approximately 83%. Competitive adsorption analysis demonstrated inverse proportionality between ionic strength and CIP retention, with trivalent cations exhibiting superior competitive displacement capacity compared to mono- and divalent counterparts. Isothermal modeling revealed multilayer adsorption mechanisms governed by hybrid chemisorption/physisorption processes in both soil and MP substrates. Spectroscopic characterization suggested differential adsorption pathways: MP-CIP interactions were primarily mediated through hydrophobic partitioning and π-π electron coupling, while soil–MP composite systems exhibited dominant cation exchange capacity and surface complexation mechanisms. Notably, electrostatic attraction/repulsion forces modulated adsorption efficiency across all experimental conditions, particularly under varying pH regimes. This work advances understanding of co-contaminant dynamics in soil ecosystems, informing risk assessment frameworks. Full article

Space charge injection in polypropylene (PP) significantly weakens the stability of HVDC cables. Impact polypropylene copolymer (IPC) is often used as insulation material for AC cables, but in the DC field, IPC has the problem of space charge accumulation. This is because there is a multi-phase structure inside the IPC to which ethylene monomer was added in the production process, and the difference in physicochemical properties of each phase is an important reason for the accumulation of space charge inside the material. In this work, the vinyl phases and propenyl phases of two types of IPC were separated. The film samples were prepared and tested at 30 °C and 50 °C for DC electrical conductivity, and at 30 °C, 50 °C, and 80 °C for space charge. The experimental results show that the DC conductivity of vinyl phases is significantly higher than that of propenyl phases in both types of IPC. The degrees of mismatch between the DC conductivity of vinyl phase and that of propenyl phase are different in the two types of IPC, and the mismatch degree of DC conductivity is from several times to hundreds of times. The conductivity of the two vinyl samples is ohmic. The conductivity of the two propenyl phases shows nonlinearity under different electric field intensity, and the mismatch degree of the two phases increases with temperature. Compared to untreated IPC, at all test temperatures, the maximum space charge density of the propenyl samples is much lower, which can be reduced by about 1/3 at 50 °C and by about 50% at 80 °C. The density of heteropolar charge produced by impurity ionization in the samples and the depth of electrode injection both decreased. At each temperature, the distortion rate of the electric field in propenyl samples is lower than that in IPC, the distortion rate can be reduced by more than 15%, and the distortion rate can be reduced by nearly half at 80 °C. The charge dissipation characteristic of propenyl samples during depolarization is also optimized compared with IPC samples, the time required for charge dissipation to reach stability is shortened, and the residual charge density in the sample is reduced at the end of depolarization. In addition, the relevance between the variation of DC conductivity of phases and space charge characteristics was discussed according to SCLC (space charge limited current) theory. This work provides a feasible reference for the manufacture of high-reliability polypropylene-based cable material with excellent insulation performance. Full article

This study investigates the tensile and flexural properties of self-reinforced polylactic acid (SrPLA) and poly(ethylene terephthalate) (SrPET) for prosthetic socket applications. These self-reinforced polymer (srP) composites utilize both a matrix and reinforcement made from the same material, resulting in an optimal matrix–interface bond that significantly enhances mechanical properties compared to traditional bulk polymers and composites. Prosthetic sockets serve as a critical interface between an amputee’s residuum and the prosthetic components, such as pylons and feet. Conventional socket materials, including monolithic high-density polyethylene and polypropylene, as well as advanced fillers reinforced with thermoset resins, often fall short in strength or affordability, particularly for amputees in low- to middle-income countries. In this study, we employed srP composites with various architectural stitch densities, aiming to achieve superior material properties. The results demonstrate that these materials exhibit higher strength and strain capabilities than many existing prosthetic materials. Notably, the low-density srPET composites achieved a tensile strength of 85.11 MPa and a strain of 19.7%, while high-density srPLA exhibited a failure strength of 36.65 MPa and a strain of 1.4%. Additionally, our findings reveal that the stiffness of both srPLA and srPET increases as the density of the reinforcement decreases. Overall, this study suggests that srP composites represent a viable and sustainable alternative for the manufacturing of prosthetic sockets, offering both enhanced performance and cost-effectiveness. Full article

This study investigated the optimal combination of compatibilizers and stabilizers to enhance the value of marine environment plastic (MEP). The composition of the plastics was analysed, and a simulated recycled plastic blend (sMEP) was prepared based on a simplified composition of actual MEP. Different concentrations of three commercial compatibilizers (C1, C2 and C3) were tested to improve tensile strength. The tensile tests indicated that the blend compatibilized with 10 wt.% C3 (polypropylene grafted with maleic anhydride) exhibited the highest increase in tensile strength. This optimal compatibilization was then combined with two commercial stabilizers and applied to a simulated MEP blend. Scanning electron microscopy images showed that all blends had a continuous polyethylene phase with dispersed poly(ethylene terephthalate) (PET) and polypropylene (PP) droplets. The simulated blend with 10 wt.% C3 exhibited a reduced PET droplet size in the dispersed phase. Differential scanning calorimetry results revealed a decrease in polyethylene crystallinity and an increase in PP crystallinity. The improved properties of the blend were attributed to the effectiveness of the C3 compatibilizer in enhancing the interface between the PP and PET phases. An effective formulation was developed to valorise marine-sourced plastics by leveraging existing scientific knowledge and accessible commercial additives. Applying this enhanced formulation to real MEP not only demonstrated its effectiveness, but also highlighted a practical approach for reducing plastic pollution and supporting circular economy principles, contributing to environmental conservation efforts. Full article

This study describes the physicochemical characterisation of interpenetrating hydrogel networks (IHNs) composed of either poly(hydroxyethylmethacrylate, p(HEMA)) or poly(methacrylic acid, p(MAA)), and Pluronic block copolymers (grades F127, P123 and L121). IHNs were prepared by mixing the acrylate monomer with Pluronic block copolymers followed by free radical polymerisation. p(HEMA)–Pluronic blends were immiscible, evident from a lack of interaction between the two components (Raman spectroscopy) and the presence of the glass transitions (differential scanning calorimetry, DSC) of the two components. Conversely, IHNs of p(MAA) and each Pluronic were miscible, displaying a single glass transition and secondary bonding between the carbonyl group of p(MAA) and the ether groups in the Pluronic block copolymers (Raman and ATR-FTIR spectroscopy). The effect of storage of the IHNs in Tris buffer on the physical state of each Pluronic and on the loss of Pluronic from the IHNs were studied using DSC and gravimetric analysis, respectively. Pluronic loss from the IHNs was dependent on the grade of Pluronic, time of immersion in Tris buffer, and the nature of the IHN (p(HEMA) or p(MAA)). At equilibrium, the loss was greater from p(HEMA) than from p(MAA) IHNs, whereas increasing ratio of poly(propylene oxide) to poly(ethylene oxide) decreased Pluronic loss. The retention of each Pluronic grade was shown to be primarily due to its micellization; however, hydrogen bonding between Pluronic and p(MAA) (but not p(HEMA)) IHNs contributed to their retention. Full article

Acetylene and methylacetylene are impurities commonly found in the raw materials used for the production of polymers such as polypropylene and polyethylene. Experimental evidence indicates that both acetylene and methylacetylene can decrease the productivity of the Ziegler-Natta catalyst and alter the properties of the resulting polymer. However, there is still a lack of understanding regarding the mechanisms through which these substances affect this process. Therefore, elucidating these mechanisms is crucial to develop effective solutions to this problem. In this study, the inhibition mechanisms of the Ziegler-Natta catalyst by acetylene and methylacetylene are presented and compared with the incorporation of the first propylene monomer (chain initiation) to elucidate experimental effects. The Density Functional Theory (DFT) method was used, along with the B3LYP-D3 functional and the 6-311++G(d,p) basis set. The recorded adsorption energies were −11.10, −13.99, and −0.31 kcal mol⁻¹, while the activation energies were 1.53, 2.83, and 28.36 kcal mol⁻¹ for acetylene, methylacetylene, and propylene, respectively. The determined rate constants were 4.68 × 10¹¹, 5.29 × 10¹¹, and 2.3 × 10⁻⁸ M⁻¹ s⁻¹ for acetylene, methylacetylene, and propylene, respectively. Based on these values, it is concluded that inhibition reactions are more feasible than propylene insertion only if an ethylene molecule has not been previously adsorbed, as such an event reinforces propylene adsorption. Full article