Search Results (584)

The increasing incidence of oil contamination in many aquatic ecosystems, particularly in oil-rich regions such as Qatar, poses significant threats to marine life and human activities. Our study addresses the critical need for effective and eco-friendly oil-water separation techniques, focusing on developing graphene and chitosan-based three-dimensional (3D) polymeric sponges. These materials have demonstrated potential due to their high porosity and surface area, which can be enhanced through surface treatment to improve hydrophobicity and oleophilicity. This study introduces a new technique dependent on the optimization of the graphene oxide (GO) concentration within the composite sponge to achieve a superior oil uptake capacity (51.4 g oil/g sponge at 3% GO), and the detailed characterization of the material’s performance in separating heavy oil-water emulsions. Our study seeks to answer key questions regarding the performance of these modified sponges and their scalability for industrial applications. This research directly aligns with Qatar’s environmental goals and develops sustainable oil-water separation technologies. It addresses the pressing challenges of oil spills, ultimately contributing to improved marine ecosystem protection and efficient resource recovery. Full article

The purpose of this study was to demonstrate the feasibility of using spheroidal cellulose powders with different particle sizes (2 and 7 µm) in face creams and to evaluate their effect on selected physicochemical and performance properties of these products. A series of prototypes of facial creams with spheroidal cellulose were prepared. The following tests were carried out: stability, dynamic viscosity, texture analysis, degree of skin hydration, and evaluation of sensory appeal by consumers. It was observed that none of the creams showed instability over time. The addition of powdered spheroidal cellulose was found to increase dynamic viscosity and hardness and reduce the adhesion strength of the tested emulsions to the base face cream. A positive effect of the presence of polymeric raw materials on the level of skin hydration was observed. The most favorable results were obtained for the E4 cream prototype containing spheroidal powders of both 2 and 7 µm particle size at a weight ratio of 2.5 to 2.5. In addition, according to the members of the sensory panel, the E4 face cream was best evaluated and showed sensory benefits. The study concluded that spheroidal cellulose powders are a promising biodegradable alternative to microplastics in cosmetics. Full article

Polymers containing biocidal moieties (e.g., amino or ammonium groups) are considered promising materials that can help combat the growing resistance of pathogens to commonly used antimicrobials. Searching for new polymeric biocides, in this work, non-porous and porous poly(hydromethylsiloxane) (PHMS) networks were prepared and post-functionalized by N-allylaniline (Naa). Non-porous networks were obtained by cross-linking PHMS in the bulk and porous—in W/O high-internal-phase emulsion (HIPE). Linear divinyldisiloxane (M₂^Vi) or cyclic tetravinyltetrasiloxane (D₄^Vi) were used as cross-linkers. Studies confirmed the expected non-porous and open macroporous microstructure of the initial networks. They also showed that functionalization by Naa was more efficient for the non-porous networks that swelled to lower extents in toluene and contained higher amounts of Si-H groups than the porous ones. In the reactions with benzyl chloride or 1-bromoctane, some amino groups present in these materials were transformed to ammonium groups. It was found that activity against Gram-positive S. aureus and Gram-negative E. coli bacteria depended on the functionalization degree, cross-linking level and the microstructure of the modified materials. Full article

Polymeric composite solutions (PCSs) reinforced with carbon nanotubes sponges (CNT-sponges) have attracted interest in material science and engineering due to their physicochemical properties. Understanding the influence of CNT-sponges content (0.1 wt.%, 0.3 wt.% and 0.5 wt.%) on rheological behavior of poly(styrene-co-acrylonitrile) P(S:AN) (0:100, 20:80, 40:60 and 50:50, wt.%:wt.%) solutions synthesized by emulsion polymerization can predict the viscoelastic parameters for their possible application in electrospinning processes. The obtained nanofibers can be used as sensors, textiles, purifying agents or artificial muscles and tissues. For this, amplitude and frequency sweeps were performed to measure the viscosity (η), storage (G’) and loss (G”) moduli and loss factor (tan δ). Most PCSs showed a shear thinning behavior over the viscosity range of 0.8 < η/Pa·s < 20. At low CNT-sponges concentration in the polymer matrix, the obtained loss factor indicated a liquid-like behavior, while as CNT-sponges content increases, the solid-like behavior predominated. Then, the polymeric solutions were successfully electrospun; however, some agglomerations were formed in materials containing 0.5 wt.% of CNT-sponges attributed to the interaction forces generated within the structure. Finally, the rheological analysis indicates that the PCS with a low percentage of CNT-sponges are highly suitable to be electrospun. Full article

A simple and innovative synthesis strategy was established to produce polymer microspheres with a distinctive walnut-like morphology, incorporating Fe₃O₄ nanoparticles within their structure. This was achieved through γ-ray-initiated mini-emulsion polymerization. To ensure high encapsulation efficiency, the surface of the Fe₃O₄ nanoparticles was chemically altered to shift their wettability from hydrophilic to hydrophobic, enabling uniform dispersion within the monomer phase before polymerization. The formation of the walnut-like architecture was found to be significantly influenced by both the polymerization dynamics and phase separation, as well as the shrinkage of the crosslinked polymer network formed between the monomer and the resulting polymer. Divinylbenzene (DVB) was chosen as the monomer due to its ability to generate a mechanically stable polymer framework. The γ-ray irradiation effectively initiated polymerization while preserving structural coherence. A detailed analysis using FTIR, SEM, and TEM confirmed the successful fabrication of the Fe₃O₄-loaded polymer microspheres with their characteristic textured surface. Moreover, magnetic characterization via vibrating sample magnetometry (VSM) indicated pronounced superparamagnetic behavior and strong magnetic responsiveness, highlighting the potential of these microspheres for advanced biomedical applications. Full article

The aim of this study was to develop and characterize UV-crosslinked hydrogel matrices based on polyethylene glycol diacrylate (PEGDA), gum arabic, betaine, and sodium alginate for potential bioanalytical applications. Various physicochemical analyses were performed, including pre-polymerization emulsion stability (Multiscan), FT-IR spectroscopy, swelling behavior in physiological buffers, pH monitoring, contact angle measurements, and morphological assessment via SEM and optical microscopy. The results demonstrated that both alginate content and UV exposure time significantly influence the structural and functional properties of the hydrogels. The highest swelling ratio (2.32 g/g) was observed for the formulation containing 5% sodium alginate polymerized for 5 min (5SA_5), though this sample showed mechanical fragmentation during incubation. In contrast, the most balanced performance was achieved for the 10SA_15 formulation, which maintained structural integrity and exhibited a swelling ratio of 1.92 g/g after 9 days. The contact angle analysis revealed a surface hydrophilicity range from 50° to 100°, with the lowest angle (50°) recorded for 10SA_5, indicating high surface wettability. These findings confirm the suitability of such hydrogels for biomedical applications, particularly as absorbent, stable platforms for drug delivery or wound healing. Full article

Nose-to-brain drug delivery is an innovative approach that leverages the unique anatomical pathways connecting the nasal cavity to the brain, including the olfactory and trigeminal nerve routes. This method bypasses the blood–brain barrier, enabling direct and efficient transport of therapeutic agents to the central nervous system. It offers significant advantages, such as rapid drug action, reduced systemic side effects, and improved patient compliance through non-invasive administration. This entry summarizes factors affecting the nose-to-brain delivery of drugs and the recent development of nanoparticle-based nose-to-brain delivery. Full article

In order to improve oil recovery efficiency in low-permeability reservoirs, this study developed amphiphilic Janus-SiO₂ nanoparticles to prepare polymer gel microspheres for enhanced oil recovery (EOR). Firstly, Janus-SiO₂ nanoparticles were synthesized via surface modification using (3-aminopropyl)triethoxysilane and α-bromoisobutyryl bromide. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) characterization confirmed the successful grafting of amino and styrene chains, with the particle size increasing from 23.8 nm to 32.9 nm while maintaining good dispersion stability. The Janus nanoparticles exhibited high interfacial activity, reducing the oil–water interfacial tension to 0.095 mN/m and converting the rock surface wettability from oil-wet (15.4°) to strongly water-wet (120.6°), thereby significantly enhancing the oil stripping efficiency. Then, polymer gel microspheres were prepared by reversed-phase emulsion polymerization using Janus-SiO₂ nanoparticles as emulsifiers. When the concentration range of nanoparticles was 0.1–0.5 wt%, the particle size range of polymer gel microspheres was 316.4–562.7 nm. Polymer gel microspheres prepared with a high concentration of Janus-SiO₂ nanoparticles can ensure the moderate swelling capacity of the particles under high-temperature and high-salinity conditions. At the same time, it can also improve the mechanical strength and shear resistance of the microspheres. Core displacement experiments confirmed the dual synergistic effect of this system. Polymer gel microspheres can effectively plug high-permeability zones and improve sweep volume, while Janus-SiO₂ nanoparticles enhance oil displacement efficiency. Ultimately, this system achieved an incremental oil recovery of 19.72%, exceeding that of conventional polymer microsphere systems by more than 5.96%. The proposed method provides a promising strategy for improving oil recovery in low-permeability heterogeneous reservoir development. Full article

Hydrogel particles, renowned for their high water content and biocompatibility in drug delivery and tissue engineering, typically rely on complex, costly microfluidic systems to reach sub 5 µm dimensions. We present a vortex-based inverse-emulsion polymerization strategy in which UV crosslinking of polyethylene glycol diacrylate (PEGDA) dispersed in n-hexadecane and squalene yields tunable micro- and nanogels while delineating the parameters that govern particle size and uniformity. Systematic variation in surfactant concentration, vessel volume, continuous phase viscosity, vortex speed and duration, oil-to-polymer ratio, polymer molecular weight, and pulsed vortexing revealed that increases in surfactant level, vortex intensity/duration, vessel volume, and oil-to-polymer ratio each reduced mean diameter and PDI, whereas higher polymer molecular weight and continuous phase viscosity broadened the size distribution. We further investigated how these same parameters can be tuned to shift particle populations between nano- and microscale regimes. Under optimized conditions, microhydrogels achieved a coefficient of variation of 0.26 and a PDI of 0.07, with excellent reproducibility, and nanogels measured 161 nm (PDI = 0.05). This rapid, cost-effective method enables precise and scalable control over hydrogel dimensions using only standard laboratory equipment, without specialized training. Full article

To address the deficiencies of traditional emulsified asphalt-pavement maintenance material in cohesive strength, high-temperature rutting resistance, as well as adhesion to aggregates, this study developed waterborne epoxy resin-modified emulsified asphalt (WEA) binders using a two-component waterborne epoxy resin (WER) and systematically investigated their modification mechanisms and pavement performance. The results indicated that WER emulsions and curing agents could polymerize to form epoxy resin within the emulsified asphalt dispersion medium, with the modification process dominated by physical interactions. When the WER content exceeded 12%, a continuous modifier network structure was established within the emulsified asphalt. The epoxy resin formed after curing could significantly increase the polarity component of the binder, thereby increasing the surface free energy. The linear viscoelastic range of the WEA binder exhibited a negative correlation with the dosage of the WER modifier. Notably, when the WER content exceeded 6%, the high-temperature stability (rutting resistance and elastic recovery performance) of the binder was significantly enhanced. Concurrently, stress sensitivity and frequency dependence gradually decrease, demonstrating superior thermomechanical stability. Furthermore, WER significantly enhanced the interfacial interaction and adhesion between the binder and aggregates. However, the incorporation of WER adversely affects the low-temperature cracking resistance of the binder, necessitating strict control over its dosage in practical applications. Full article

Polymer flooding is one of the critical methods for enhancing oil recovery (EOR) in domestic and international oilfields. Since the large-scale implementation of industrial polymer flooding in Daqing Oilfield in 1996, the overall recovery rate has increased by over 10%. With the advancement of chemical flooding technologies, conventional polymer flooding can no longer meet the practical demands of oilfield development. This study focuses on functional polymers, such as salt-resistant polymers and polymeric surfactants, tailored for Class II and III reservoirs in Daqing Oilfield. A series of experiments, including emulsification experiments, hydrodynamic characteristic size-reservoir compatibility comparison experiments, polymer retention experiments in porous media, and core flooding experiments, were conducted to investigate the differences between functional polymers and conventional polymers in terms of intrinsic properties and application performance. Comparative analyses of molecular chemical structures and micro-aggregation morphologies between functional polymers (branched polymers and polymeric surfactants) and conventional polymers revealed structural composition disparities and distinct viscosity-enhancing properties. From the perspective of aqueous solution viscosity enhancement mechanisms, functional polymers exhibit a three-stage viscosity-enhancing mechanism: bulk viscosity, associative viscosity, and emulsion-induced viscosity enhancement. The hydrodynamic characteristic sizes of polymers were analyzed to evaluate their compatibility with reservoir pore structures, and the seepage resistance mechanisms of both polymeric surfactants and salt-resistant polymers were identified. Core flooding experiments conclusively demonstrated the superior practical performance of functional polymers over conventional polymers. The application of functional polymers in polymer flooding can effectively enhance oil recovery. Full article

In the field of water-based inks, the use of alkali-soluble resins (ASRs) as polymeric surfactants for synthesizing polyacrylate latexes has become a mainstream method. This study first designed and prepared crosslinkable ASRs with a diacetone acrylamide (DAAM) crosslinking monomer via emulsion polymerization. These ASRs were then employed as surfactants to synthesize self-crosslinking polyacrylate latexes through an in situ one-pot method, systematically investigating the influence of crosslinkable ASRs on the properties of the corresponding polyacrylate latexes. The research revealed that all prepared polyacrylate latexes exhibited a core–shell structure. With increasing DAAM content in the ASRs, the latex particle size gradually increased while the particle size distribution narrowed. All latexes demonstrated excellent stability, with absolute ζ-potential values exceeding 30 mV. The introduction of DAAM into ASRs significantly increased the glass transition temperature in the high-temperature region of the corresponding latex films, with the tensile strength reaching a maximum of 7.96 MPa. Moderate crosslinking in ASRs substantially improved the water resistance of latex films. Crosslinking degree tests indicated that latex films prepared through either single shell-layer crosslinking or single core-layer crosslinking showed relatively low crosslinking degrees, while only the dual core–shell crosslinking strategy could effectively enhance the film crosslinking degree. However, excessively crosslinked shell layers significantly hindered the crosslinking reaction of DAAM in the core layer, leading to reduced overall film crosslinking. Additionally, incorporating a certain number of DAAM crosslinking groups in ASRs was found to improve the adhesion of corresponding water-based inks on PE and BOPP substrates, with adhesion on BOPP substrates reaching up to 100%. Full article

Traditional approaches to constructing thermally conductive networks typically necessitate costly equipment and intricate processes, rendering them unsuitable for mass production and commercialization. Here, we propose a facile strategy to construct highly oriented boron nitride/polyacrylate pressure-sensitive adhesive frameworks by a calendering process. A UV light-based bulk polymerization method is adopted to prepare the pressure-sensitive adhesives (PSAs), which makes the preparation process solvent-free and volatile organic compound (VOC)-free, and environmentally friendly compared to emulsion and solvent-based pressure-sensitive adhesives. This simple, economical and scalable method provides new ideas and ways for the preparation of advanced thermal conductive networks. The highly oriented and flexible m-BNNSs/polyacrylate pressure-sensitive adhesive composites (m-BNNSs/PSAs-Ori) exhibited a significantly high thermal conductivity (TC) of 0.9552 W/(m·K) at 25 wt% filler content. Significantly, m-BNNSs/PSAs-Ori composites showed a better thermal response than the single-layer thermally conductive pressure-sensitive adhesive. Moreover, the composites also possess excellent electrical insulation and mechanical properties. This exploration not only provides a reasonable design scheme for thermal interface materials, but also promotes the practical application of polyacrylate pressure-sensitive adhesive composites in thermal management. Full article

The development of eco-friendly surfactants is pivotal for enhanced oil recovery (EOR). In this study, a novel lignin-derived zwitterionic surfactant (DMS) was synthesized through a two-step chemical process involving esterification and free radical polymerization, utilizing renewable alkali lignin, maleic anhydride, dimethylamino propyl methacrylamide (DMAPMA), and sulfobetaine methacrylate (SBMA) as precursors. Comprehensive characterization via ¹H NMR, FTIR, and XPS validated the successful integration of amphiphilic functionalities. Hydrophilic–lipophilic balance (HLB) analysis showed a strong tendency to form stable oil-in-water (O/W) emulsions. The experimental results showed a remarkable 91.6% viscosity reduction in Xinjiang heavy crude oil emulsions at an optimum dosage of 1000 mg/L. Notably, DMS retained an 84.8% viscosity reduction efficiency under hypersaline conditions (total dissolved solids, TDS = 200,460 mg/L), demonstrating exceptional salt tolerance. Mechanistic insights derived from zeta potential measurements and molecular dynamics simulations revealed dual functionalities: interfacial modification by DMS-induced O/W phase inversion and electrostatic repulsion (zeta potential: −30.89 mV) stabilized the emulsion while disrupting π–π interactions between asphaltenes and resins, thereby mitigating macromolecular aggregation in the oil phase. As a green, bio-based viscosity suppressor, DMS exhibits significant potential for heavy oil recovery in high-salinity reservoirs, addressing the persistent challenge of salinity-induced inefficacy in conventional chemical solutions and offering a sustainable pathway for enhanced oil recovery. Full article

CO₂-responsive polymers have emerged as a significant class of smart materials, distinguished by their ability to reversibly alter their properties upon exposure to CO₂. Due to CO₂’s abundant availability, low cost, non-toxicity, energy efficiency, and excellent biocompatibility, these polymers offer remarkable environmental and practical advantages. This review succinctly explores recent advancements in the synthesis, mechanisms, and applications of CO₂-responsive polymers, emphasizing the pivotal roles of specific acidic and basic functional groups such as carboxylic acids, phenolic groups, amines, amidines, guanidines, and imidazoles. Advanced polymerization techniques including free radical polymerization (FRP), atom transfer radical polymerization (ATRP), reversible addition-fragmentation chain transfer (RAFT), and nitroxide-mediated polymerization (NMP) are critically evaluated for their precision and flexibility in polymer design. Significant applications in smart separation, carbon capture, drug delivery, desalination, emulsions, tissue engineering, and sensing technologies are discussed comprehensively. Although substantial progress has been made, ongoing challenges include enhancing response speed, durability, sustainability, and economic viability. Future research is recommended to focus on innovative polymer structures, computational modeling, hybrid materials, and greener synthesis methods. This review aims to inspire continued exploration and practical utilization of CO₂-responsive polymers to address pressing environmental and technological needs. Full article