Search Results (258)

In this study, we designed a statistical polyampholyte bearing cationic quaternary ammonium salts and anionic phosphate groups as pendant functionalities. In addition, small amounts of o-nitrobenzyl groups, which generate anionic species upon photoirradiation, were introduced into the pendant chains to prepare a photo-responsive polyampholyte via reversible addition-fragmentation chain transfer radical polymerization. By increasing the feed ratio of the cationic monomer during copolymerization, a polyampholyte with a net positive charge was obtained. Upon photoirradiation of the aqueous solution of this cationic polyampholyte, the fraction of negatively charged groups in the polymer increased, resulting in a decrease in the zeta potential from positive values to around 0 mV. When the photo-responsive cationic polyampholyte was mixed with an anionic polyelectrolyte, poly(2-acrylamido-2-methylpropanesulfonate) (PAMPS), in water, micrometer-sized coacervate droplets were formed via electrostatic interactions. Photoirradiation of the aqueous coacervate system increased the fraction of negative charges in the polyampholyte, thereby weakening the electrostatic interactions with anionic PAMPS and resulting in the dissociation of the coacervates. Overall, this study presents a design guideline for polymeric materials in which interpolymer electrostatic interactions can be controlled by light to induce the disappearance of coacervates. Full article

Poly(ethylene terephthalate) (PET) is a widely used commodity polymer owing to its low cost, excellent mechanical properties, and high processability. Chemical modification of PET surfaces to impart specific functionalities represents an effective strategy for transforming PET into high-value-added materials without altering its bulk properties. In this study, we investigated the surface functionalization of PET substrates using surface-initiated atom transfer radical polymerization (SI-ATRP). ATRP initiation sites were introduced onto PET surfaces through mild surface hydrolysis followed by polyethyleneimine coating. To further enhance the grafting density, an inimer-based strategy was employed, in which a bifunctional monomer containing both a polymerizable group and a latent initiation site was used to form hyperbranched polymer structures on the PET surface, thereby amplifying the number of active initiation sites. Using these modified PET substrates, SI-ATRP of functional methacrylate monomers was successfully carried out. Grafting of poly(2,2,2-trifluoroethyl methacrylate) imparted highly hydrophobic surface properties, yielding water contact angles above 120°, whereas grafting of poly([2-(methacryloyloxy)ethyl]trimethylammonium chloride) produced hydrophilic surfaces with contact angles below 20°. Surface characterization by X-ray photoelectron spectroscopy confirmed successful graft polymerization and effective surface coverage. While the macroscopic wettability was primarily governed by the chemical nature of the grafted polymers, the inimer-based initiation-site amplification significantly enhanced the surface electrostatic properties of the polycationic polymer–grafted surfaces, increasing the ζ-potential from approximately +20 mV to over +100 mV. Antibacterial tests using Escherichia coli K-12 as a model bacterium demonstrated that PET substrates grafted with poly([2-(methacryloyloxy)ethyl]trimethylammonium chloride) exhibited clear contact-active antibacterial activity, achieving up to 2-log reduction in viable bacterial counts after 3 h of contact incubation. These results highlight the importance of molecular-level control of grafting architecture and surface electrostatic properties in the design of functional antibacterial PET surfaces. Full article

Nitrogen pollution poses significant risks to both environmental systems and human health. Iron-based autotrophic denitrification offers a green and cost-effective strategy for nitrogen removal, but is often accompanied by the accumulation of undesirable byproducts. A nitrogen removal system combining anammox with iron-based autotrophic denitrification was constructed in this study to investigate the enhancement effect of anaerobic ammonium-oxidizing bacteria (AnAOB). The results showed that during the stable operation phase, nitrate removal efficiencies reached 91.45% and 84.29% for groups A (0.5 g/L AnAOB) and B (0.1 g/L AnAOB), respectively, significantly higher than the 62.87% observed in the control group. Furthermore, the experimental groups exhibited markedly reduced accumulation of ammonium byproducts. Microbial community analysis revealed that AnAOB addition increased microbial richness and diversity, and promoted community shifts that favored nitrogen removal. Notably, even low dosages of AnAOB yielded strong performance enhancements, underscoring the economic viability of this integrated approach. Structural characterization using SEM, XRD, and XPS indicated that system performance deterioration in the later stages was primarily due to cell encrustation and iron passivation. Electrochemical analyses further demonstrated that iron passivation impaired electron transfer on the filler surface, thereby reducing denitrification efficiency, whereas extracellular polymeric substances (EPS) did not exhibit such inhibitory effects. These findings provide both mechanistic insight and practical guidance for the design and optimization of anammox-enhanced iron-based denitrification systems. Full article

Oral administration of tocotrienol has poor systemic distribution due to poor selectivity by the α-tocopherol transfer protein at the liver. Local injection of tocotrienols with appropriate drug delivery systems is significant to ensure that the drug is delivered directly to the site of injury or fracture. This paper presents a tocotrienol-loaded gelatin hydrogel crosslinked with genipin for bone regeneration. This innovative method improves the incorporation and sustained delivery of tocotrienol while overcoming its incompatibility with hydrophilic biomaterials. It establishes a novel platform for targeted therapeutic applications in bone treatment. The cytotoxicity and physicochemical properties of tocotrienol were examined using the genipin-crosslinked gelatin hydrogel. A 10% tocotrienol nanoemulsion (TTE) was prepared using a sonicator and characterized with a zeta sizer and FTIR. A dose–response analysis was conducted to determine the appropriate tocotrienol concentration for hydrogel integration with gelatin (7% or 10% w/v) and crosslinked with genipin (0.1% or 0.3% w/v). The dose–response study’s tocotrienol nanoemulsion was added to gelatin before polymerization. With 141.9 nm particles and 0.150 PDI, the nanoemulsion was homogeneous and stable. The 1% tocotrienol nanoemulsion was chosen due to its viability. Formulations 1% TTE_0.1% GNP_7% GEL and 1%TTE_0.3% GNP_7% GEL had superior physicochemical properties compared to other groups. The 1% TTE_0.3% GNP_7% GEL had outstanding hydrophilicity, low weight loss, and a suitable swelling ratio for bone application. SEM scans of the surface and cross-section showed that 1% TTE_0. 3% GNP_7% GEL had interconnected pores with an optimal average pore size of 292 ± 37 μm. Adding tocotrienol to the gelatin hydrogel matrix did not affect FTIR, XRD, or EDX. In vitro cytotoxicity studies indicated >90% cell viability of hFOB 1.19 cells cultured on 1% TTE_0.1% GNP_7% GEL and 1% TTE_0.3% GNP_7% GEL (105 ± 4.36% and 95.36 ± 9.78%). Combining tocotrienol with a genipin-crosslinked gelatin hydrogel demonstrated superior physicochemical properties and no in vitro toxicity. Full article

Nanogels provide unique opportunities for stabilizing fragile enzymes through soft, hydrated polymer networks. Here, we report the development of a glutathione peroxidase (GPx)-loaded nanogel (GPxNG) engineered via a mild “grafting-to” epoxy–amine coupling strategy to enhance enzyme stability and antioxidant function. An amphiphilic copolymer composed of methacrylated 2,2,6,6-tetramethyl-4-piperidyl (PMA) and glycidyl methacrylate (GMA) was synthesized by controlled reversible addition–fragmentation chain-transfer (RAFT) polymerization using a poly(ethylene glycol) (PEG) macro-chain transfer agent (macro-CTA), yielding well-defined polymer chains with reactive epoxy groups. Covalent conjugation between polymer epoxides and GPx enzyme surface amines generated soft, PEGylated nanogels with high coupling efficiency, uniform particle sizes, and excellent colloidal stability. The engineered nanogels exhibited shear-thinning injectability, robust storage stability, and non-cytotoxic behavior in RAW 264.7 macrophages. Compared with native GPx enzyme, GPxNGs demonstrated significantly enhanced reactive oxygen species (ROS) scavenging activity, including strong inhibition of lipid peroxidation and copper-induced low-density lipoprotein (LDL) oxidation. Importantly, the nanogels preserved GPx enzyme activity after extended storage, freeze–thaw cycles, and repeated catalytic use, whereas the free enzyme rapidly lost function. This protective effect arises from the nanoscale confinement of the GPx enzyme within the flexible PEG-based network, which limits unfolding and aggregation. Overall, this work introduces a simple and biocompatible “grafting-to” nanogel platform capable of stabilizing redox-active enzymes without harsh conditions. The GPx nanogels combine high enzymatic preservation, potent antioxidant activity, and excellent handling properties, highlighting their potential as a therapeutic nanoplatform for mitigating oxidative stress-associated disorders such as atherosclerosis. Full article

Bio-gels are a class of functional polymeric materials with three-dimensional network structures. Their exceptional biocompatibility, biodegradability, high specific surface area, and tunable physicochemical properties make them highly promising for environmental remediation. This article systematically reviews the classification of bio-gels based on source, cross-linking mechanisms, and functional attributes. It also elaborates on their fundamental properties such as porous structure, high water absorbency, stimuli-responsiveness, and mechanical stability and examines how these properties influence their environmental remediation efficiency. This review comprehensively analyze the mechanisms and efficacy of bio-gels in adsorbing heavy metal ions, removing organic dyes, improving soil water retention, and restoring ecosystems. Special attention is given to the interactions between surface functional groups and contaminants, the role of porous structures in mass transfer, and the ecological effects within soil–plant systems. Additionally, this review explores extended applications of bio-gels in medical tissue engineering, controlled release of drugs and fertilizers, and enhanced oil recovery, highlighting their versatility as multifunctional materials. Finally, based on current progress and challenges, this review outline key future research directions. These include elucidating microscopic interaction mechanisms, developing low-cost renewable feedstocks, designing multi-stimuli-responsive structures, improving long-term stability, and establishing full life-cycle environmental safety assessments. These efforts will help advance the efficient, precise, and sustainable use of bio-gels in environmental remediation, offering innovative solutions to complex environmental problems. Full article

Herein, we report a combined computational and experimental investigation into the recently reported universal pyrazole-based reversible addition-fragmentation chain transfer (RAFT) agents (Z−C(=S)−S−R, where Z is 3,5-dimethyl-1H-pyrazol-1-yl), which can mediate controlled radical polymerization of a broad scope of monomers without the need for an additional initiator or catalyst. The results reveal that the high molar absorption coefficient and efficient photolysis kinetics of pyrazole-based chain transfer agents (CTAs) under blue light (${\lambda }_{\max }$ = 465 nm) enable rapid radical generation, underpinning ultrafast polymerization of acrylates, acrylamides, methacrylates, and N-vinylpyrrolidone (NVP). While the efficient light absorption is attributed to structural dissimilarity between the Z group and the S–R group (which breaks the local symmetry of the C=S group), the fast photolysis originates from favorable $\pi$ electron donation from the Z group to the C=S group. Meanwhile, the $\pi$ electron donation is still weaker than in xanthates, which explains the excellent control of a wide range of monomers, except methacrylates. This work establishes design principles for next-generation CTAs for ultrafast and monomer-universal photoiniferter RAFT polymerization. Full article

Anion exchange membranes (AEMs) are vital for electrochemical energy devices such as alkaline fuel cells and water electrolyzers, enabling the use of non-precious metal catalysts despite challenges from alkaline degradation. Hyperbranched polymers (hbPs) with their globular structure, high functional group density, and simple synthesis, offer a promising platform for enhancing transport and stability. In this study, multifunctional hbPs were synthesized from 4-vinylbenzyl chloride (VBC) and 2-hydroxyethyl methacrylate (HEMA) via atom transfer radical self-condensing vinyl polymerization (ATR-SCVP) and crosslinked into polyurethane-based AEMs. Characterization confirmed successful copolymerization and crosslinking, with excellent alkaline stability. Membranes crosslinked with higher molecular weight (MW) and VBC-richer hbPs (e.g., OH-hbP1-PU) exhibited high water uptake (75%) but low ion-exchange capacity (1.54 mmol/g) and conductivity (186 µS/cm), attributed to steric hindrance and insufficient ionic network connectivity. In contrast, OH-hbP2-PU exhibited optimal properties, with the highest OH⁻ conductivity (338 µS/cm) and IEC (2.64 mmol/g), highlighting a balanced structure for efficient ion transport. This work offers a tunable strategy for high-performance AEM development through tailored hbP architecture. Full article

Stimuli-responsive polymers (SRPs) have garnered significant attention in recent decades due to their immense potential in biomedical and environmental applications. When these SRPs are grafted onto magnetic nanoparticles, they form multifunctional nanocomposites capable of various complex applications, such as targeted drug delivery, advanced separations, and magnetic resonance imaging. In this study, we employed a one-step hydrothermal method using 3-aminopropyltrimethoxysilane (APTES) to synthesize APTES-modified Fe₃O₄ nanoparticles (APTES@Fe₃O₄) featuring reactive terminal amine groups. Subsequently, via two consecutive surface-initiated atom transfer radical polymerizations (SI-ATRP), pH- and temperature-responsive polymer blocks were grown from the Fe₃O₄ surface, resulting in the formation of poly(itaconic acid)-block-poly(N-isopropyl acrylamide) (PIA-b-PNIPAM)-grafted nanomagnetic particles (PIA-b-PNIPAM@Fe₃O₄). To confirm the chemical composition and assess how the particle morphology and size distribution of these SRP-based nanocomposites change in response to ambient pH and temperature stimuli, various characterization techniques were employed, including transmission electron microscopy, differential light scattering, and Fourier transform infrared spectroscopy. The results indicated successful synthesis, with PIA-b-PNIPAM@Fe₃O₄ demonstrating sensitivity to both temperature and pH. Full article

Polymer brushes (PBs) are transformative surface-modifying nanostructures, yet their synthesis via controlled methods like copper-mediated surface-initiated atom-transfer radical polymerization (Cu⁰-SI-ATRP) faces reproducibility challenges due to a lack of understanding of parameter interdependencies. This study systematically evaluates the Cu⁰-SI-ATRP process for polyacrylamide brushes (PAM-PBs), aiming to clarify key parameters that influence the synthesis process. This evaluation followed a step-by-step characterization that tracked molecular changes through infrared spectroscopy (IR) and surface development by contact angle (CA) through two different mixing methods: ultrasonic mixing and process simplification (Method A) and following literature-based parameters (Method B). Both methods, consisting of surface activation, 3-aminopropyltriethoxysilane (APTES) deposition, bromoisobutyryl bromide (BiBB) anchoring, and polymerization, were analyzed by varying parameters like concentration, temperature, and time. Results showed ultrasonication during surface activation enhanced siloxane (1139→1115 cm⁻¹) and amine (1531 cm⁻¹) group availability while reducing APTES concentration to 1 Vol% without drying sufficed for BiBB anchoring. BiBB exhibited insensitivity to concentration but benefited from premixing, evidenced by sharp C–Br (~1170 cm⁻¹) and methyl (3000–2800 cm⁻¹) bands. Additionally, it was observed that PAM-PBs improved with Method A, which had reduced variance in polymer fingerprint regions compared to Method B. Adding to the above, CA measurements gave complementary step-by-step information along the modifications of the surface, revealing distinct wettability behaviors between bulk PAM and synthesized PAM-PBs (from 51° to 37°). As such, this work identifies key parameter influence (e.g., mixing, BiBB concentration), simplifies steps (drying omission, lower APTES concentration), and demonstrates a step-by-step, systematic parameter decoupling that reduces variability. In essence, this detailed parameter analysis addresses the PAM-PBs synthesis process with better reproducibility than the previously reported synthesis method and achieves the identification of characteristic behaviors across the step-by-step process without the imperative need for higher-cost characterizations. Full article

Proton exchange membranes are widely used in environmentally friendly applications such as fuel cells and electrochemical hydrogen compression. In these applications, an ideal proton exchange membrane should have both excellent proton conductivity and mechanical strength. Polymer proton exchange membranes, such as sulfonated poly(ether ether ketone) (SPEEK) membranes with high ion exchange capacity, can lead to higher proton conductivity. However, the ionic groups may reduce the interaction between polymer segments, lower the membrane’s mechanical strength, and even cause it to dissolve in water as the temperature exceeds 55 °C. The porous graphitic C₃N₄ (Pg–C₃N₄) nanosheet is an important two–dimensional polymeric carbon–based material and has a high content of –NH₂ and –NH– groups, which can interact with the sulfonic acid groups in the sulfonated SPEEK polymer, form a more continuous proton transfer channel, and inhibit the movement of the polymer segment, leading to higher proton conductivity and mechanical strength. In this study, we found that a SPEEK membrane containing 3% Pg–C₃N₄ nanosheets achieves the optimized proton conductivity of 138 mS/cm (80 °C and 100% RH) and a mechanical strength of 74.1 MPa, improving both proton conductivity and mechanical strength by over 50% compared to the SPEEK membrane. 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

Novel amphiphilic block copolymers of N-vinyl pyrrolidone (NVP) and either n-hexyl methacrylate (HMA, PNVP-b-PHMA) or stearyl methacrylate (SMA, PNVP-b-PSMA) were prepared by RAFT polymerization techniques and the sequential addition of monomers starting from the polymerization of NVP and using two different Chain Transfer Agents, CTAs. PNVP-b-PHMA are amorphous block copolymers containing constituent blocks with both high and low Tg values, whereas PNVP-b-PSMA are amorphous–semi-crystalline copolymers. Samples with different molecular weights and compositions were obtained. The copolymers were microphase-separated, but partial mixing was also observed. The presence of the amorphous PNVP block reduced the crystallinity of the PSMA blocks in the PNVP-b-PSMA copolymers. The thermal stability of the blocks was influenced by both constituents. The self-assembly behavior in THF, which is a selective solvent for polymethacrylate blocks, and in aqueous solutions, where PNVP was soluble, was examined. Unimolecular or low-aggregation-number micelles were obtained in THF for both types of samples. On the contrary, high-aggregation-number, spherical, and compact micelles were revealed in aqueous solutions. The increase in the steric hindrance of the side ester group of the polymethacrylate chain led to slightly lower degrees of association. The hydrophobic compound curcumin was efficiently encapsulated within the micellar core of the supramolecular structures in aqueous solutions. Micelles with higher aggregation numbers were more efficient in the encapsulation of curcumin. The results of this study were compared with those obtained from other block copolymers based on PNVP. Full article

This paper elucidates the consecutive chain transfer reaction, initially to (p-vinylphenyl) methyl dichlorosilane (or (p-vinylbenzyl) methyl dichlorosilane), followed by hydrogen, during metallocene-catalyzed propylene polymerization by an isospecific metallocene catalyst (i.e., rac-dimethylsilylbis(2-methyl-4-phenylindenyl)zirconium dichloride, I)/ activated with methylaluminoxane (MAO), rendering a catalytic access styryldichlorosilane capped isotactic polypropylenes (iPP). The PP molecular weight is inversely related to the molar ratio of [(p-vinylphenyl) methyl dichlorosilane]/[propylene] and [(p-vinylbenzyl) methyl dichlorosilane]/[propylene]. Every polypropylene chain formed presents a terminal (p-vinylphenyl) methyl dichlorosilane (or (p-vinylbenzyl) methyl dichlorosilane) unit. Hydrogen enhances the concentration of the starting arm polymer for the subsequent synthesis of the star polymer by increasing the incorporation of the chain terminal group. In order to create star polymers with isotactic polypropylene(iPP) as the arm and a siloxane cross-linking structure as the core, the terminal dichlorosilane iPP unit can work up (with water) to create cyclic siloxane oligomer interlinkages between iPP chains. Full article

A novel efficient barium sulfate scale inhibitor was designed by examining important quantum parameters such as adsorption energy, solubility, steric hindrance parameter, and entanglement molecular weights. Through molecular simulation techniques, it was found that the carboxylic acid group of the scale inhibitor molecule could transfer an average of 0.07 e⁻ electrons to the barium sulfate surface. During molecular dynamics simulations, closer adsorption between oxygen atoms and barium ions in the scale inhibitor was observed, which resulted from van der Waals forces. Based on the simulation results at the molecular level, we successfully prepared this scale inhibitor by free radical polymerization and verified its high efficiency in our experiments: the scale inhibition efficiency was as high as 89.1% when used at a concentration of 160 mg/L under the conditions of pH = 7 and 70 °C. In addition, by SEM and XRD analyses, we further confirmed the consistency of the scale inhibition mechanism of the scale inhibitor with the molecular simulation results. Full article