Search Results (341)

A metal-ion-free method was developed to prepare κ-carrageenan/cellulose hydrogel beads for efficient cationic dye removal. The beads were fabricated using a mixture of 1-ethyl-3-methylimidazolium acetate and N,N-dimethylformamide as the solvent system, followed by aqueous ethanol-induced phase separation. This process eliminated the need for metal-ion crosslinkers, which typically neutralize anionic sulfate groups in κ-carrageenan, thereby preserving a high density of accessible binding sites. The resulting beads formed robust interpenetrating polymer networks. The initial swelling ratio reached up to 28.3 g/g, and even after drying, the adsorption capacity remained over 50% of the original. The maximum adsorption capacity for crystal violet was 241 mg/g, increasing proportionally with κ-carrageenan content due to the higher surface concentration of anionic sulfate groups. Kinetic and isotherm analyses revealed pseudo-second-order and Langmuir-type monolayer adsorption, respectively, while thermodynamic parameters indicated that the process was spontaneous and exothermic. The beads retained structural integrity and adsorption performance across pH 3–9 and maintained over 90% of their capacity after five reuse cycles. These findings demonstrate that κ-carrageenan/cellulose hydrogel beads prepared via a metal-ion-free strategy offer a sustainable and effective platform for cationic dye removal from wastewater, with potential for heavy metal ion adsorption. Full article

This paper reviews the fundamental principles and techniques of nickel electrodeposition, with a particular focus on metallizing polymeric substrates. It outlines the electrochemical mechanisms involved in depositing nickel from an acidic Watts bath, detailing the roles of key electrolyte components—i.e., nickel sulfate, nickel chloride, and boric acid—and the influence of process parameters, such as current density, temperature, and pH, on deposit quality (density and surface condition) and mechanical properties. In addressing the unique challenges posed by non-conductive polymers, this review compares emerging methods like silver conductive paint, highlighting differences in deposition time, surface resistivity, and environmental impact. Additionally, this paper examines how process parameters affect the as-deposited microstructure, adhesion, and overall mechanical properties (such as hardness, ductility, and tensile strength), while identifying critical issues such as low deposition density and substrate degradation. These insights provide a structured background for optimizing electroplating processes for applications in electronics, automotive, aerospace, and biomedical sectors, and suggest future research directions to enhance deposition uniformity, sustainability, and process control. Full article

Traditional cementitious coating materials struggle to meet the performance criteria for protective coatings in complex environments. This study developed a polymer-modified cement-based coating material with polymer, silica fume (SF), and quartz sand (QS) as the principal admixtures. It also investigated the influence of material composition on the coating’s mechanical properties, durability, interfacial bond characteristics with concrete, and the durability enhancement of coated concrete. The results demonstrated that compared with ordinary cementitious coating material (OCCM), the interfacial bonding performance between 3% Styrene Butadiene Rubber Powder (SBR) coating material and concrete was improved by 42%; the frost resistance and sulfate erosion resistance of concrete protected by 6% polyurethane (PU) coating material were improved by 31.5% and 69.6%. The inclusion of polymers reduces the mechanical properties. The re-addition of silica fume can lower the porosity while increasing durability and strength. The coating material, mixed with 12% SF and 6% PU, exhibits mechanical properties not lower than those of OCCM. Meanwhile, the interfacial bonding performance and durability of the coated concrete have been improved by 45% and 48%, respectively. The grey relational analysis indicated that the coating material with the best comprehensive performance is the one mixed with 12% SF + 6% PU, and the grey correlation degree is 0.84. Full article

The aim of this study is to explore the feasibility of using flotation wastewater from copper–porphyry ore processing to synthesize a gel that serves as a precursor for a polymer nanocomposite used in supercapacitor electrode fabrication. These wastewaters—characterized by high acidity and elevated concentrations of metal cations (Cu, Ni, Zn, Fe), sulfates, and organic reagents such as xanthates, oil (20 g/t ore), flotation frother (methyl isobutyl carbinol), and pyrite depressant (CaO, 500–1000 g/t), along with residues from molybdenum flotation (sulfuric acid, sodium hydrosulfide, and kerosene)—are byproducts of copper–porphyry gold-bearing ore beneficiation. The reduction of Ni powder in the wastewater induces the degradation and formation of a gel that captures both residual metal ions and organic compounds—particularly xanthates—which play a crucial role in the subsequent steps. The resulting gel is incorporated during the oxidative polymerization of aniline, forming a nanocomposite with a polyaniline matrix and embedded xanthate-based compounds. An asymmetric supercapacitor was assembled using the synthesized material as the cathodic electrode. Electrochemical tests revealed remarkable capacitance and cycling stability, demonstrating the potential of this novel approach both for the valorization of industrial waste streams and for enhancing the performance of energy storage devices. Full article

Polymer application combined with nitrogen (N) fertilization can increase soil N transformation efficiency. However, the mechanism of polymer influencing soil biocommunity characteristics and nitrogen transformation is still unclear. In this field experiment, a self-developed water-soluble polymer material (PPM, a mixture of anionic polyacrylamide, polyvinyl alcohol, and manganese sulfate) was combined with N fertilization N100 (300 kg/hm² of N), PN100 (PPM + 300 kg/hm² of N), and PN80 (PPM + 240 kg/hm² of N) to investigate soil biodiversity, enzyme activities, and metabolomics. The results showed that under the application of PPM, the contents of soil total nitrogen (TN), alkali hydrolyzable nitrogen (ANS), nitrate nitrogen, organic carbon (SOC), and microbial biomass nitrogen (MBN) increased with a decrease in the N application rate, while soil bulk density, pH, and EC (electrical conductivity) decreased. The Chao 1 index of soil bacterial and nematode communities of the PN80 treatment was 30.6% and 10.7% higher than that of the N100 treatment, respectively, and the Shannon index was 2.72% and 2.64% higher than that of the N100 treatment, respectively. In the short term, the application of PPM affected the structure and composition of soil bacterial and nematode communities. In particular, the relative abundances of omnivorous (Aporcelaimellus) and bacterivorous (Prismatolaimus) nematodes were significantly higher than those of the N100 treatment. These changes further regulated the soil metabolites, promoting soil nitrogen transformation. This study will provide a scientific basis for nitrogen reduction in drip-irrigated wheat planting in arid regions. Full article

To improve the construction performance of inorganic adhesives used for bonding fiber-reinforced polymer (FRP) sheets to reinforce concrete structures, make rational use of resources, and reduce carbon emissions, double-shear tests on the interface bonding performance between bonded FRP sheets and cement mortar test blocks, as well as four-point bending tests on bonded carbon fiber-reinforced polymers (CFRPs) to reinforce concrete beams, were conducted using basic magnesium sulfate cement (BMSC) as the adhesive. The influence laws of parameters, such as the type of FRP sheet and the number of FRP sheet bonding layers on the shear performance of the bonding interface between BMSC and cement mortar test blocks, were investigated, as well as the influence laws of the number of CFRP sheet bonding layers and the type of binder on the bending performance of CFRP sheet-reinforced beams. The test results show that the ultimate load of CFRP-reinforced beams bonded with BMSC as the binder increased by 17.4% to 44.4% compared with the unreinforced beams and simultaneously improved the flexural stiffness and crack-limiting ability of the reinforced beams. The failure of the reinforced beam begins with the separation of the CFRP sheet from the concrete at the middle and bottom of the beam span. When the CFRP sheet of the reinforced beam is one layer and two layers, the flexural bearing capacity reaches 91.4% and 96%, respectively, of the reinforced beam, with epoxy resin as the binder under the same conditions. With the increase in the number of CFRP layers, the flexural bearing capacity of the reinforced beam improves, but the increased flexural bearing capacity does not increase proportionally with the increase in the number of sheet layers. By introducing the influence coefficient of BMSC on the flexural bearing capacity (FBC) of reinforced beams, based on the test results, the formula for calculating the FBC of concrete beams, which are reinforced with CFRP sheets bonded by BMSC, was developed. After verification, the calculation formulas established in this paper have high accuracy and can provide theoretical references for similar engineering applications. Full article

Current hydrogels used for cartilage tissue engineering often lack the mechanical strength and structural integrity required to mimic native human cartilage. This study addresses this limitation by developing reinforced hydrogels based on a ternary polymer blend of poly(vinyl) alcohol (PVA), gelatin (GL), and chitosan (CH), with gentamicin sulfate (GS) as an antimicrobial agent and a crosslinker. The hydrogels were produced using two crosslinking methods, the freeze/thaw and heated cycles, and reinforced with forcespun polycaprolactone (PCL) nanofiber to improve mechanical performance. Chemical characterization revealed that GS forms weak hydrogen bonds with the ternary polymers, leading to esterification with PVA, and covalent bonds are formed as the result of the free amino group (-NH₂) of chitosan that reacts with the carboxylic acid group (-COOH) of gelatin. SEM images help us to see how the hydrogels are reinforced with polycaprolactone (PCL) fibers produced via force spinning technology, while mechanical properties were evaluated via uniaxial tensile and compressive tests. Water retention measurements were performed to examine the crosslinking process’s influence on the hydrogel’s water retention, while the hydrogel surface roughness was obtained via confocal microscopy images. A constitutive model based on non-Gaussian strain energy density was introduced to predict experimental mechanical behavior data of the hydrogel, considering a non-monotonous softening function. Loading and unloading tests demonstrated that GS enhanced crosslinking without compromising water retention or biocompatibility because of the reaction between the free amino group of CH and the carboxylic group of gelatin. The PCL-reinforced PVA/GL/CH hydrogel shows strong potential for cartilage repair and tissue engineering applications. Full article

Polymer concrete (PC) is recognized for its lightweight nature, wear resistance, and rapid curing, making it well-suited for the repair of deteriorated infrastructure. This research critically addresses the challenge of enhancing overlay adhesion to compromised substrates by uniquely evaluating the role of pristine versus functionalized multi-walled carbon nanotubes (MWCNTs) in improving polymer concrete (PC) bond strength, particularly on concrete deteriorated by sulfate attack. PC mixtures containing varying concentrations of MWCNTs (0%, 0.25%, and 0.5% by weight) were prepared and tested for their mechanical properties, including compressive strength, modulus of rupture, and pull-off strength. Pull-off tests were conducted to assess the bond between PC overlays and Portland cement concrete (PCC) substrates. To examine the effects of substrate deterioration, PCC specimens were cured under two conditions: standard and sulfate-exposed environments. The results showed that neat polymer concrete (PC-Neat) achieved a high average pull-off strength of 2.82 MPa under normal conditions. Incorporating 0.25% pristine MWCNTs (PC-P25) significantly reduced the bond strength to 0.039 MPa. In contrast, improved performance was observed with functionalized MWCNTs. The addition of 0.5% COOH-functionalized MWCNTs (PC-FC50) yielded a pull-off strength of 2.22 MPa under normal conditions and 1.65 MPa in sulfate environments. Notably, under sulfate exposure, functionalized MWCNTs enhanced the bond strength by up to 15% compared to PC-Neat, highlighting their potential in aggressive environments. This distinct improvement in bond strength presents a significant finding, demonstrating a novel pathway for developing more resilient repair materials for infrastructure exposed to aggressive chemical environments. Full article

Although the intercalation of sericite with cationic surfactants has been extensively studied, successful intercalation using anionic surfactants has yet to be achieved. This article aims to partially or fully intercalate sericite with an anionic surfactant, and to develop the corresponding sericite/polymer nanocomposite. To achieve this goal, we modified raw sericite by thermal modification, acid activation, and sodium modification. The modified sericite was then co-intercalated by cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and anionic surfactant sodium dodecyl sulfate (SDS). The intercalated sericite was characterized by XRD, FTIR, SEM, DTA-TG, and a contact angle tester. The optimized sample had a layer-to-layer distance of 6.56 nm and an intercalation rate of 95.7%. Compared with raw sericite, the new organo-sericite showed increased hydrophobicity. A proposed mechanism for the intercalation by these surfactants was also discussed. Finally, sericite/epoxy composite was prepared by using the new organo-sericite as the raw material, demonstrating significantly improved mechanical properties compared to pure epoxy resin (72% improved for bending strength and 62% improved for tensile strength, compared with pure epoxy resin). The new organo-sericite is a promising filler in epoxy resin to enhance thermal stability and mechanical performance of the composite. Full article

Phosphorus contamination in water bodies is a major contributor to eutrophication, leading to algal overgrowth, oxygen depletion, and ecological imbalance. Conventional treatment methods, including chemical precipitation and synthetic adsorbents, are often limited by high operational costs, low biodegradability, and secondary pollutant generation. In this study, a cationic starch was synthesized through free radical graft polymerization of 3-methacrylamoylaminopropyl trimethyl ammonium chloride (MAPTAC) onto corn starch. The modified polymer exhibited a high degree of substitution (DS = 1.24), indicating successful functionalization with quaternary ammonium groups. Theoretical calculations using zDensity Functional Theory (DFT) at the B3LYP/6-311+G(d,p) level revealed a decrease in chemical hardness (from 0.10442 eV to 0.04386 eV) and a lower ionization potential (from 0.24911 eV to 0.15611 eV) in the modified starch, indicating enhanced electronic reactivity. HOMO-LUMO analysis and molecular electrostatic potential (MEP) maps confirmed increased electron-accepting capacity and the formation of new electrophilic sites. Experimentally, the cationic starch showed stable zeta potential values averaging +15.3 mV across pH 5.0–10.0, outperforming aluminum sulfate (Alum), which reversed its charge above pH 7.5. In coagulation-flocculation trials, the modified starch achieved 87% total suspended solids (TSS) removal at a low coagulant-to-biomass ratio of 0.0601 (w/w) using Scenedesmus obliquus, and 78% TSS removal in real wastewater at a 1.5:1 ratio. Additionally, it removed 30% of total phosphorus (TP) under environmentally benign conditions, comparable to Alum but with lower chemical input. The integration of computational and experimental approaches demonstrates that MAPTAC-modified starch is an efficient, eco-friendly, and low-cost alternative for nutrient and solids removal in wastewater treatment. Full article

Drought is a major environmental constraint that negatively affects crop germination, seedling establishment, and overall yield. This study presents a sustainable approach to improving wheat productivity under water-deficit conditions through the application of a gellan gum-based hydrogel enriched with the growth stimulant. The hydrogel was synthesized by inducing ionic gelation of gellan gum using potassium chloride and ammonium sulfate, forming a robust, cross-linked polymer network. Wheat seeds were coated with one to eight layers of the hydrogel using a sequential dipping and drying process. Optimal seedling performance was achieved with a two-layer coating, balancing sufficient water retention with adequate gas exchange. FTIR spectroscopy and pH analysis confirmed ionic interactions between Kaz-6 and the carboxyl groups of gellan, supporting its stable incorporation within the polymer matrix. Mechanical characterization showed that ammonium sulfate significantly enhanced gel strength and cross-linking density compared to potassium chloride. Laboratory germination assays and greenhouse trials demonstrated that seeds coated with gellan hydrogel containing Kaz-6 showed enhanced germination rates, greater biomass accumulation, and significantly improved drought tolerance—surviving up to 10 days longer than controls under water-limited conditions. These findings highlight the potential of biopolymer-based hydrogels as eco-friendly seed coating materials that can improve crop resilience and productivity in arid environments. The proposed formulation aligns with sustainable agriculture goals and represents a promising direction for future field-scale applications in climate-adaptive farming systems. Full article

Recent studies focus on recovering materials from Waste Electrical and Electronic Equipment (WEEE). Printed Circuit Boards (PCBs) are promising due to their heterogeneous composition, which includes precious metals, ceramics, and polymers. This research analyzes the leaching process of computer PCB waste to recover valuable metals such as copper and gold. The study involved physical-mechanical processing of PCB samples followed by chemical composition characterization. Metal extraction was performed through a three-stage leaching process. The first two stages used 2 M and 3 M sulfuric acid with hydrogen peroxide as leaching agents, achieving about 75% copper extraction. In the third stage, parameters for gold leaching using thiosulfate were evaluated, including concentrations of ammonium hydroxide and copper sulfate, reaction times (1–4 h), and temperatures (30, 40, and 50 ${\phantom{­}}^{\circ }$C). The leaching solution comprising 0.12 M sodium thiosulfate, 0.2 M ammonium hydroxide, and 20 mM copper sulfate yielded maximum gold extractions of 14.76% for fine and 15.73% for coarse fractions at 40 ${\phantom{­}}^{\circ }$C. In conclusion, the proposed method for recovering metals from PCBs can reduce the environmental impact of improper WEEE disposal while promoting a circular economy of secondary raw materials. Full article

Background: Ulcerative colitis (UC), a subtype of chronic inflammatory bowel disease (IBD), is primarily treated with oral medications to reduce inflammation and alleviate symptoms. Celecoxib (CXB) is an attractive candidate for UC; however, its limited solubility and low bioavailability pose significant challenges to its clinical application. Methods: We reported a novel chondroitin sulfate A–Celecoxib (CSA-CXB) polymeric nanoprodrug to address the limited solubility and low bioavailability of CXB. CXB was conjugated to chondroitin sulfate A (CSA) via succinic anhydride (SA) and ethylenediamine to prepare CSA-CXB polymers, which can self-assemble into nanoparticle structural prodrugs in aqueous condition. We investigated the stability, blood compatibility, and responsiveness of the nanoparticles. The ability of the nanoparticles to treat UC in vitro and in vivo was then evaluated. Results: The CSA-CXB nanoprodrug was spherical with a mean particle size of 188.4 ± 2.2 nm, a zeta potential of −22.9 ± 0.1 mV, and sustained drug release behavior. Furthermore, CSA-CXB exhibited remarkable antioxidant and anti-inflammatory effects, as it can significantly increase the free radical scavenging rate and reduce the expression level of ROS, TNF-α, IL-6, nitric oxide (NO), and COX-2 protein in vitro. In vivo results demonstrated that CSA-CXB targeted the mice’s colon efficiently mitigate UC symptoms by inhibiting the expression of inflammatory cytokine. Conclusions: The CSA-CXB nanoprodrug can improve the therapeutic impact of CXB, and has potential as a new preparation for a clinical UC treatment nanoprodrug. Full article

Theranostic nanoparticles integrate diagnostic and therapeutic potential, representing a promising approach in precision medicine. Accordingly, numerous inventions have been patented to protect novel formulations and methods. This review examines the evolution of patented theranostic nanoparticles, focusing on organic nanosystems, particularly polymeric and lipid nanoparticles, to assess their development, technological advances, and patentability. A scoping review approach was conducted following the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines in the World Intellectual Property Organization (WIPO) and European Patent Office (EPO) database. The search included patents filed within the last ten years (2014–2024) that specifically claimed organic and/or hybrid theranostic nanoparticles. Data extraction focused on nanoparticle composition, synthesis methods, functionalization strategies, and theranostic applications. The search identified 130 patents, of which 13 met the inclusion criteria. These patents were primarily filed by inventors from the United States, Canada, Great Britain, Italy, and China. Polymeric nanoparticles were frequently engineered for targeted drug delivery and imaging, utilizing hyperbranched polyesters, sulfated polymers, or chitosan-based formulations. Lipid nanoparticles were often hybridized with inorganic nanomaterials or magnetic nanostructures to enhance their theranostic potential. While most patents detailed synthesis methods and physicochemical characterizations, only a few provided comprehensive preclinical validation, limiting their demonstrated efficacy. The analysis of recent patents highlights significant advances in the design and application of theranostic nanoparticles. However, a notable gap remains in validating these nanosystems for clinical translation. Future efforts should emphasize robust preclinical data, including in vitro and in vivo assessments, to enhance patent quality and applicability to substantiate the claimed theranostic capabilities. Full article

Polyetheretherketone (PEEK) is a high-performance, biocompatible polymer with remarkable mechanical properties, making it a promising candidate for medical implants. However, its intrinsic radiolucency poses a challenge for post-operative imaging. This study investigates the photon shielding capabilities and X-ray imaging qualities of pure PEEK and its composites with barium sulfate (BaSO₄), tantalum (Ta), bismuth oxide (Bi₂O₃), and hydroxyapatite (HA). The Monte Carlo-based Geant4 toolkit and the EpiXS application were used to evaluate key photon interaction parameters, including mass attenuation coefficients, effective atomic number (Z_eff), and effective electron density (N_eff), as well as the imaging performance metrics such as energy deposition and signal-to-noise ratio (SNR). Results indicate that high atomic number composites significantly enhance PEEK’s photon attenuation and imaging contrast. PEEK-Bi₂O₃ exhibited the highest attenuation coefficients and energy deposition, making it the most effective X-ray shielding material. PEEK-Ta provided a balanced performance with enhanced shielding and lower secondary radiation effects, making it suitable for applications requiring both radiopacity and imaging stability. PEEK-BaSO₄ moderately improved attenuation while maintaining a lower density, offering a trade-off between radiopacity and mechanical properties. Conversely, PEEK-HA demonstrated minimal enhancement in photon attenuation, limiting its effectiveness for radiographic applications. The findings suggest that incorporating high atomic number elements into PEEK significantly enhances its suitability for radiopaque medical implants, allowing for improved post-operative monitoring. Full article