Polymers最新文献

Environmental pollution, stemming from the disposal of contaminants, poses severe threats to ecosystems and human health. The emergence of a new class of pollutants, termed emerging contaminants (ECs), in soil, water, and air has raised global concerns, aligning with the UN 2030 Agenda's Sustainable Development Goals. Aerogels, three-dimensional structures with high porosity and low density, offer promise in addressing this issue. Cellulose-based aerogels, derived from abundant, renewable, and biodegradable sources, particularly stand out for their potential in adsorption applications. However, challenges arise in water and wastewater treatment due to cellulose aerogel's inherent hydrophilicity. To overcome this limitation, incorporating new components and employing modification processes becomes essential. This article explores the production phases and diverse modifications of cellulose aerogels, aiming to enhance their adsorption capabilities for various environmental contaminants. By addressing hydrophilicity issues and developing stable composites, cellulose aerogels can contribute significantly to efficient and sustainable solutions in the quest for cleaner ecosystems and improved human health.

Background: Polymethyl methacrylate (PMMA) is ideal for denture bases but is prone to biofilm accumulation, leading to denture stomatitis (DS), often involving Candida albicans. Dimethylaminohexadecyl methacrylate (DMAHDM) and 2-methacryloyloxyethyl phosphorylcholine (MPC) are introduced into dental materials for their antimicrobial and protein-repellent properties. This study investigates the effects of incorporating dimethylaminohexadecyl methacrylate (DMAHDM) and 2-methacryloyloxyethyl phosphorylcholine (MPC) into heat-polymerized (HP) and 3D-printed (3DP) denture base resins on microbial adhesion and cytotoxicity.

Methods: HP and 3DP denture base specimens were prepared using varying concentrations of DMAHDM and MPC. Microbial adhesion was quantified using CFU counts of C. albicans, and cytotoxicity was assessed via an MTT assay using fibroblast cells after 24 h, 3 days, and 7 days.

Results: Both DMAHDM and MPC significantly reduced the CFU counts in both HP and 3DP materials; the combination of 1.5% DMAHDM and 3% MPC exhibited the most substantial antimicrobial effects. Cytotoxicity results varied between materials and time points; however, all treated groups maintained cell viability above the 70% threshold, indicating no significant cytotoxic effects.

Conclusion: Incorporating DMAHDM and MPC into denture base resins can effectively reduce microbial adhesion while maintaining acceptable cytotoxicity levels.

Brucite (Mg(OH)₂) is a typical precipitate in the mining industry that adversely affects processes such as flotation and thickening. Gaining insights into the physicochemical properties of this mineral is critical for developing strategies to mitigate these challenges and improve operational efficiency. Additionally, incorporating natural-origin polymers aligns with the shift toward more sustainable mining practices. In this study, molecular dynamics simulations were employed to investigate the interaction of brucite with polysaccharides such as cellulose, guar gum, and alginate and to compare these with conventional polymers, including polyacrylamide, hydrolyzed polyacrylamide, and polyacrylic acid, under conditions of pH 11 in low-salinity water. The methodology enhanced adsorption sampling by incorporating additional temporary interactions between the polymer and the brucite surface. The results reveal that neutral polymers exhibit stronger and more stable interactions with brucite compared to charged polymers, which is consistent with the neutral nature of brucite under the studied conditions. Van der Waals forces predominantly govern the adsorption of polysaccharides, while Coulombic forces primarily drive interactions involving polyacrylamides. These findings provide valuable insights into the molecular mechanisms of polymer-brucite interactions, facilitating the development of more effective and sustainable mining additives.

This study employed a high-speed rotating crushing process to modify pyrolyzed carbon black (CBp) using self-lubricating and low-friction polytetrafluoroethylene (PTFE). The effects of PTFE content on the dispersion, mechanical properties, wear resistance, and thermal stability of modified PTFE-CBp/natural rubber (NR) composites were investigated. The rotating crushing process from the high-speed grinder altered the physical structure of PTFE, forming tiny fibrous structures that interspersed among the CBp particles. This arrangement encouraged the alignment of CBp particles in specific directions and improved the surface activity of CBp, enhancing the dispersion of CBp within the NR matrix and consequently improving wear resistance. The experimental results indicated that as the amount of PTFE fibers increased, the hardness, wear resistance, and thermal stability of the PTFE-CBp/NR composite significantly improved. Compared to untreated CBp/NR composites, the hardness, modulus at 300%, and wear resistance of the 3 phr PTFE-CBp/NR composites increased by 20%, 24%, 21%, respectively, achieving the preparation of highly wear-resistant CBp/NR composites.

Currently, in the domestic practice of retreading tires using vulcanization tanks, some tanks exhibit uneven temperature distributions leading to low retreading success rates. To address that, this paper simulated the temperature and velocity fields during the heating process of vulcanization tanks for waste tire retreading. The results indicated that a higher heating power reduces the time required for the vulcanizing agent to reach the vulcanization condition, but it also increases the difference in tire temperature in the tank, with a severely uneven distribution of the temperature field. Subsequently, to improve the uniformity of temperature distribution and enhance the retreading rate of waste tires, this paper proposed two types of orifice plates to adjust the airflow organization. The results show that both the plain orifice plate and the frustum cone orifice plate can enhance the uniformity of the temperature field within the vulcanization tank and reduce the temperature difference between tires. Moreover, at the same heating power, the presence of the orifice plates increases the rate of temperature increase in the tires and the vulcanizing agent compared to the original vulcanization tank, improving the thermal efficiency of the vulcanization tank heater.

The pequi (Caryocar brasiliense) is a typical fruit from the Brazilian Cerrado. From it, pequi pulp oil is extracted, a valuable product for cosmetic applications due to its high levels of unsaturated fatty acids and carotenoids. Carotenoids are antioxidant compounds that are easily oxidized. To improve pulp stability, emulsification techniques with carboxymethylcellulose at 1% (w/w) were used to encapsulate the pequi pulp oil at 1, 3, 5% (w/w), and 8% (w/w) of polysorbate 80^® using a high-rotation mechanical stirrer. The pequi pulp oil was first characterized by FTIR and GC-MS. The results indicated the presence of chemical groups characteristic of the oil itself and the presence of a large proportion of fatty acids, which are essential for the maintenance of cutaneous hydration and the barrier, also acting in the tissue repair process. All emulsions presented stable over 120 days with slightly acidic pH values and were compatible with human skin. The droplet diameter was less than 330 nm, and the polydispersity index was around 0.3, indicating systems with low polydispersity. The Zeta potential (ζ) exhibited negative values sufficient to stabilize the emulsified systems. All emulsions behaved as non-Newtonian fluids, presenting pseudo-plastic and thixotropic properties that are considered important for topical applications.

This study explores the use of propylene oxide-modified ethylenediamine (PPO-EDA) as a novel crosslinker and chain extender in polyurethane (PU) adhesives. PPO-EDA was synthesized and compared with N,N'-dimethylethylenediamine (DMEDA) to assess its impact on mechanical properties and adhesion performance. Key parameters such as NCO conversion, tensile strength, and lap shear strength were thoroughly evaluated. The results demonstrated that incorporating PPO-EDA significantly improved NCO conversion and crosslink density, leading to notable enhancements in tensile strength and elastic modulus compared to DMEDA. Lap shear tests further revealed superior adhesion performance in PPO-EDA-modified PU adhesives, particularly on amine silane-treated steel substrates, where lap shear strength consistently outperformed other samples. This improved performance was attributed to PPO-EDA's dual role as a chain extender and crosslinker, which strengthened the adhesive's structural integrity. This study underscores the effectiveness of PPO-EDA as a modifier for enhancing both mechanical and adhesive properties in PU-based adhesives, offering a promising solution for optimizing high-performance adhesives in automotive and industrial applications.

Poly(lactic acid) (PLA) exhibits excellent shape memory properties but suffers from brittleness and a high glass transition temperature (T_g), limiting its utility in flexible and durable applications. This study explored the modification of PLA properties through the incorporation of poly(ethylene glycol) (PEG), varying in both content (5-20 wt%) and molecular weight (4000-12,000 g/mol), to enhance its suitability for specific applications, such as medical splints. The PLA/PEG blend, containing 15 wt% PEG and with a molecular weight of 12,000 g/mol, exhibited superior shape fixity (99.27%) and recovery (95.77%) in shape memory tests conducted at a programming temperature (T_p) of 45 °C and a recovery temperature (T_r) of 60 °C. Differential scanning calorimetry (DSC) analysis provided insights into the thermal mechanisms driving shape memory behavior of the PLA/PEG blend. The addition of PEG to the PLA blend resulted in a reduction in T_g and an increase in crystallinity, thereby facilitating enhanced chain mobility and structural reorganization. These thermal changes enhanced the shape fixity and recovery of the PLA/PEG blend. Synchrotron wide-angle X-ray scattering (WAXS) was further employed to elucidate the microstructural evolution of PLA/PEG blends during the shape memory process. Upon stretching, the PLA/PEG chains aligned predominantly along the tensile direction, reflecting strain-induced orientation. During recovery, the PLA/PEG chains underwent isotropic relaxation, reorganizing into their original configurations. This structural reorganization highlighted the critical role of chain mobility and alignment in driving the shape memory behavior of PLA/PEG blends, enabling them to effectively return to their initial shape. Mechanical testing confirmed that increasing PEG content and molecular weight enhanced elongation at break and impact strength, balancing flexibility and strength. These findings demonstrated that PLA/PEG blends, especially with 15 wt% PEG at 12,000 g/mol, offer an optimal combination of shape memory performance and mechanical properties, positioning them as promising candidates for customizable and biodegradable medical applications.

CAM/CAD composites are widely used as dental restoration materials due to their resistivity to wear. The purpose of this study was to determine the effect of human gingival fibroblast cells on three different computer-aided design/computer-aided manufacturing (CAD/CAM) hybrid materials with resin-based composites (RBC) and to assess their stability following cell growth. The CAM/CAD dental materials were investigated in different conditions as follows: (i) cells (human gingival fibroblasts, HFIB-Gs) incubated over the material for each sample, denoted as A; (ii) reference, the raw material, denoted as B; and (iii) materials incubated in DMEM medium, denoted as C. We employed Vicker's hardness test, EDS, SEM, and AFM measurements as well as Raman spectroscopy to carefully characterize the surface modifications and the structural integrity of the CAM/CAD materials before and after fibroblast cell culture. The analysis of the surface in terms of morphology, roughness, structure, and plastic deformation presented no significant difference after incubation in cells or in media, proving their extraordinary stability and resilience to biofilm formation.

Quantum dot-polymer composites have the advantages of high luminescent quantum yield (PLQY), narrow emission half-peak full width (FWHM), and tunable emission spectra, and have broad application prospects in display and lighting fields. Research on quantum dots embedded in polymer films and plates has made great progress in both synthesis technology and optical properties. However, due to the shortcomings of quantum dots, such as cadmium selenide (CdSe), indium phosphide (InP), lead halide perovskite (LHP), poor water, oxygen, and light stability, and incapacity for large-scale synthesis, their practical application is still restricted. Various polymers, such as methyl methacrylate (PMMA), polyethylene terephthalate (PET), polystyrene (PS), polyvinylidene fluoride (PVDF), polypropylene (PP), etc., are widely used in packaging quantum dot materials because of their high plasticity, simple curing, high chemical stability, and good compatibility with quantum dot materials. This paper focuses on the application and development of quantum dot-polymer materials in the field of backlight displays, summarizes and expounds the synthesis strategies, advantages, and disadvantages of different quantum dot-polymer materials, provides inspiration for the optimization of quantum dot-polymer materials, and promotes their application in the field of wide-color-gamut backlight display.