Search Results (43)

In this study, a solvent-free, slow-curing, inherently flame-retardant polyurea coating was successfully developed through an optimized formulation. The novel polyurea was synthesized using mixed Schiff base latent curing agents derived from terminal polyether amines with different-number average molecular weights (D2000 and D400), methyl isobutyl ketone, and polyethyl phosphate glycol ester (OP550). Subsequently, polyurea/meta-aramid (PUA/AF) composite fabrics were fabricated via a scraping coating technique. Thermogravimetric analysis revealed enhanced char formation and reduced decomposition temperatures due to the incorporation of OP550. Comprehensive flame retardant performance was demonstrated through vertical flame testing, limiting oxygen index, and micro-scale combustion calorimetry, with results showing significantly reduced heat release rates, lower total heat release, and increased residual char. Mechanical evaluations indicated marked improvements in tearing, tensile, single-yarn tensile, and bursting forces, attributed to strong fiber–polyurea interfacial interactions, as confirmed by detailed SEM morphological analyses. Moreover, the PUA/AF composites exhibited excellent static puncture resistance and effective self-healing capability. Collectively, these advancements highlight the potential of PUA/AF composite fabrics as promising candidates for advanced protective textiles, integrating superior flame retardancy, mechanical strength, puncture resistance, and self-repairing functionality. Full article

Implant-associated infections (IAIs) are major complications in dental and orthopedic implants, potentially compromising osseointegration and eventually causing implant loosening or removal. Thus, early prevention of bacterial adhesion and biofilm formation is critical for successful long-term osseointegration. Polyetheretherketone (PEEK) exhibits excellent physicochemical properties and an elastic modulus similar to bone tissue, making it a promising material for dental and orthopedic implants. However, its inherent lack of antibacterial properties limits its ability to prevent IAIs. Herein, an antibacterial coating with controlled drug release and excellent biocompatibility is designed by immobilizing minocycline (Mino)-doped carboxymethyl chitosan (CMCS) onto the PEEK surface via a polydopamine (PDA)-mediated Michael addition and Schiff base reaction. The coating is characterized by SEM, XPS, water contact angle measurements, and in vitro Mino release assays. Antibacterial activity is evaluated using the zone of inhibition (ZOI), turbidity, and colony counting assays, while biocompatibility is assessed through a SEM analysis of cell morphology and CCK-8 assay. The results show that the Mino-modified coating is successfully fabricated on the PEEK surface, achieving sustained Mino release for up to 14 days. Among the three Mino concentrations, the PEEK-0.5Mino group demonstrates the best balance of antibacterial activity and biocompatibility, highlighting its potential for preventing IAIs in orthopedic and dental applications. Full article

Hydrogen chloride (HCl) is one of the most hazardous air pollutants and can cause significant damage to human health and the environment. Therefore, the continuous quantitative monitoring of HCl is of great practical importance. In this work, a novel triphenylamine derivative, named TPTc-DBD, with a Schiff base structure was synthesized. The molecular structure of TPTc-DBD was determined by NMR analysis, FTIR analysis and single crystal diffraction analysis. On this basis, a porous polyvinylidene fluoride (PVDF) film containing TPTc-DBD was then prepared by a spin-coating method, and its sensitivity to HCl was evaluated by naked eye and ultraviolet-visible absorption spectrum, respectively. The detection limit of the composite porous film for HCl molecules was determined to be 5.8 mg/m³. Interestingly, the composite films absorbing HCl can be reactivated by NH₃, which provides a cycle detection ability for HCl. After five testing cycles, the detection error remained below 1%. Furthermore, the microstructure of the film remained unchanged, highlighting its exceptional detection performance for HCl. Full article

Ti6Al4V alloy is one of the most widely used orthopedic implants due to its low density, high strength and good biocompatibility, but surface tribology limits its service life and performance. In this paper, a layer of dynamic double-network hydrogel based on a Schiff base bond and a hydrogen bond was grafted on the surface of Ti6Al4V alloy by the mussel chemical self-assembly method. The -NH₂ of acrylamide (AM) and -CHO of vanillin (VA) formed Schiff base bonds to form the first layer of a cross-linked network, a large number of hydrogen bonds were formed between the -OH of vanillin and the -OH of sodium alginate (SA) to provide the second layer of the cross-linked network and the network was properly regulated by introducing core–shell polymer nanoparticles (PDCS). Dynamic self-healing bonds, Schiff base bonds and hydrogen bonds endow qPDCS/SA/VA/AM hydrogels with self-healing ability, and the network structure destroyed under high strain (250%) can be rebuilt under low strain (1%). In the second cycle, G’ and G can recover almost the same value. PDCS/SA/VA/AM hydrogel coating can achieve dynamic repair through reversible Schiff base bond dissociation–recombination during friction, while 1000ppmPDCS/SA/VA/AM hydrogel coating can achieve stable friction reduction and low wear under multiple loads. Under 0.5 N load, the average friction coefficient of 1000ppmPDCS/SA/VA/AM hydrogel coating is as low as 0.157, which is 67.74% lower than the uncoated Ti6Al4V surface under the same load. Under 2 N load, 1000ppmPDCS/SA/VA/AM hydrogel coating remains stable and low-friction, and the average coefficient of friction (ACOF) can reach 0.130, which is 59.27% lower than the uncoated Ti6Al4V surface under the same load. The design idea of the hydrogel network regulated by core–shell polymer nanoparticles (PDCS) to achieve low friction and low wear provides a new strategy for biolubricating materials. Full article

The separation of high-viscosity oil–water emulsions remains a global challenge due to ultra-stable interfaces and severe membrane fouling. In this paper, SiO₂ micro–nanoparticles coated with polyethyleneimine (PEI) were initially loaded onto a stainless steel substrate. This dual-functional design simultaneously modifies surface roughness and wettability. Furthermore, a covalent crosslinking network was created through the Schiff base reaction between PEI and glutaraldehyde (GA) to enhance the stability of the membrane. The membrane exhibits extreme wettability, superhydrophilicity (WCA = 0°), and underwater superoleophobicity (UWOCA = 156.9°), enabling a gravity-driven separation of pump oil emulsions with 99.9% efficiency and a flux of 1006 L·m⁻²·h⁻¹. Moreover, molecular dynamics (MD) simulations demonstrate that the SiO₂-PEI-GA-modified membrane promotes the formation of a stable hydration layer, reduces the oil–layer interaction energy by 85.54%, and exhibits superior underwater oleophobicity compared to the unmodified SSM. Efficiency is maintained at 99.8% after 10 cycles. This study provides a scalable strategy that combines covalent crosslinking with hydrophilic particle modification, effectively addressing the trade-off between separation performance and membrane longevity in the treatment of viscous emulsions. Full article

Synthesis of uniform and stable electrochromic films on a conductive layer is one of the effective ways to construct high-performance electrochromic devices. The development of more convenient and feasible polymer film preparation technology is important and necessary. Herein, we demonstrated the development of a continuous in situ polymerization method to prepare electrochromic film on ITO glass through Schiff base condensation of a tetraamine Fe-based complex and organic di-/tri-aldehyde precursors. The electrochromic film was successfully coated on the surface of the ITO conductive layer and exhibited uniform morphology and excellent stability. Film P1 exhibited two reversible redox processes allowing two steps of electrochromic processes, including the oxidation of Fe(II) to Fe(III) at 1.05 V and oxidation of triphenylamine moieties to cation radicals at 1.4 V, which induced three stable color states from initial yellow to orange red and blue. The utilization of the so-formed polymer film for the fabrication of electrochromic devices gave rise to excellent electrochromic performance of fast response time of 0.4−1.2 s and high coloration efficiencies of 241.5−352.9 cm²/C at 1.9 V (at 535 nm) and 2.5 V (at 755 nm). The present work provides a new feasible strategy for constructing polymer films for high-performance electrochromic devices. Full article

A novel Schiff base ligand (L), bearing N₂O₂ donor sites, was derived from the condensation of 5-chloromethylisophthaldehyde and phenylpropanolamine (PPA). Mononuclear Co(II), Cu(II), and Zn(II) complexes were synthesized and were characterized by FTIR, UV–Vis, ¹H NMR, ESI-mass spectroscopy, molar conductance, and thermal and electrochemical studies. The thermal investigation revealed that the complexes were stable up to 150–250 °C and began to degrade in stages, resulting in the development of respective metal oxides. The Coats–Redfern integration method was used to calculate the kinetic and thermodynamic parameters, the energy of activation (Ea), and changes in enthalpy (∆H), entropy (∆S), and free energy (∆G) for each step of the degradation processes. For stage I decomposition, the calculated activation energy values of the complexes follow the order of Ea [Cu(L)] > Ea [Co(L)(H₂O)₂] > Ea [Zn(L)]. The influence of the temperature on the efficacy of antioxidant activities of the complexes with DPPH assay, ABTS assay, and hydroxy radical assay was investigated at various concentrations using ascorbic acid (AA) as the reference. Antioxidant activity was assessed at multiple temperatures to ascertain whether these complexes may be applied in radiation therapy enhanced with hyperthermia and found to be stable. Subsequently, the Cu(II) complex (C2) demonstrated a greater cytotoxicity (IC₅₀ = 5.16 µM) than Co(II), Zn(II), and conventional cisplatin when in vitro cytotoxicity was evaluated against the MCF-7 cell line using the MTT method. Analyses of the thermal stability and ROS scavenging ability of complexes have demonstrated that these complexes have potential in hyperthermic radiation therapy. Full article

Surgical resection is the primary treatment for melanoma; however, preventing tumor recurrence after resection remains a significant clinical challenge. To address this, we developed a multifunctional nanocomposite hydrogel (H-CPG) composed of glucose oxidase (GOx)-coated CuS@PDA@GOx (CPG) nanoparticles, aminated hyaluronic acid (HA-ADH), and oxidized rhizomatous polysaccharides (OBSP), which are interconnected through hydrogen bonds and dynamic Schiff base linkages. In the acidic tumor micro-environment, the hydrogel releases GOx, catalyzing the production of hydrogen peroxide (H₂O₂), which enhances chemokinetic activity through a Cu²⁺-mediated Fenton-like reaction. This process generates hydroxyl radicals that intensify oxidative stress and promote macrophage polarization from the M2 to M1 phenotype. This polarization triggers the release of pro-inflammatory cytokines, thereby inhibiting tumor recurrence. Additionally, the hydrogel induces photothermal effects that help eradicate residual bacteria at the wound site. Overall, the H-CPG hydrogel offers a dual mechanism to prevent melanoma recurrence and reduce resistance to monotherapy, presenting a promising strategy for postoperative tumor management. Full article

The functionalized graphene oxide (GO)-based composites as fillers added into organic coatings are desired for realizing the longstanding corrosion protection of carbon steel. Here, the pH-responsive two-dimensional/three-dimensional (2D/3D) GO-based composite (ZIF–90–AAP/GO) was developed by environmentally friendly corrosion inhibitor 4-aminoantipyrine (AAP) anchored on the in situ growth of zeolite imidazolate framework–90 (ZIF–90) on the GO surface (ZIF–90/GO) through the Schiff base reaction. The active filler (ZIF–90–AAP/GO) was incorporated into an epoxy coating (EP) to obtain a high-performance self-healing coating on the surface of carbon steel. ZIF–90–AAP can greatly improve dispersion and compatibility of GO in EP. The low-frequency impedance modulus of ZIF–90–AAP/GO–EP can still reach up to 1.35 × 10¹⁰ Ω⋅cm² after 40 days, which is about three orders of magnitude higher than that of the EP containing GO (GO–EP) relying on its passive and active corrosion protection. Meanwhile, ZIF–90–AAP/GO–EP exhibits excellent self-healing performance. The self-healing rate of ZIF–90–AAP/GO changes from negative to positive after 24 h, which results from the effective corrosion inhibition activity of ZIF–90–AAP for carbon steel based on the pH-triggered controlled release of AAP. The developed pH-responsive 2D/3D GO-based composite coating is very attractive for the corrosion protection of carbon steel. Full article

In recent years, the application of polyvinyl chloride (PVC) material has significantly expanded within the realm of biomedical materials. However, the hydrophobicity of PVC has been found to cause many adverse reactions in patients within the biomedical field. It is imperative to urgently discover viable approaches for enhancing the hydrophilicity of PVC in order to ensure its safety in biomedical applications. In this study, the surface of PVC films was modified with a combination of hyperbranched polylysine (HBPL) and polydopamine (pDA) through either simultaneous deposition with polydopamine (PVC-pDA/HBPL) or successive deposition of pDA and HBPL (PVC-pDA-HBPL), aiming to investigate the influence of this modification method on surface hydrophilicity enhancement. The surface coatings were characterized using gravimetry, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, and water contact angle measurements. The results demonstrated that the incorporation of HBPL led to a significant enhancement in both the deposition amount and stability of pDA, particularly when the mass ratio of DA/HBPL was approximately 1:1. Simultaneously, the morphology of the films exhibited an increase in roughness, while surface hydrophilicity was significantly enhanced upon incorporating pDA and HBPL, and the water contact angle was decreased to 43.2°. Moreover, the detachment of PVC-pDA/HBPL and PVC-pDA-HBPL after exposure to 1.0 M NaOH solutions was considerably lower compared to that of PVC-pDA alone, indicating improved stability under strongly basic conditions. Notably, these enhancements were more pronounced for PVC-pDA/HBPL than for PVC-pDA-HBPL, indicating that HBPL may act as a cross-linker during pDA deposition primarily through intermolecular Schiff base reactions, hydrogen bonding, or Michael addition. This work represents a pioneering effort in integrating HBPL and dopamine for hydrophilic modification of PVC materials, thereby expanding the potential applications of PVC materials. Additionally, we provide novel insights into constructing a hydrophilic surface based on bionic principles and expanding the potential applications of HBPL and pDA. Full article

A new Schiff base (H₂L) generated from sulfamethazine (SMT), as well as its novel micro- and nanocomplexes with Ni(II) and Cd(II) metal ions, have been synthesized. The proposed structures of all isolated solid compounds were identified with physicochemical, spectral, and thermal techniques. Molar conductance studies confirmed that the metal complexes are not electrolytic. The molecular geometry located at the central metal ion was found to be square planar for the NiL₂ and tetrahedral for the CdL₂ complexes. The kinetic and thermal parameters were obtained using the Coats and Redfern approach. Coriandrum sativum (CS) in ethanol was used to create the eco-friendly Ni and Cd nanocomplexes. The size of the obtained nanoparticles was examined using PXRD and TEM, and found to be in the sub-nano range (3.07–4.61 nm). Furthermore, the TEM micrograph demonstrated a uniform and homogeneous surface morphology. The chemistry of the prepared nanocomplexes was studied using TGA and TEM techniques. The effect of temperature on the prepared nanocomplexes’ size revealed a decrease in size by heating. Furthermore, the nanocomplexes’ antimicrobial and anticancer properties were evaluated. The outcomes demonstrated that the nanocomplexes exhibited better antimicrobial properties. Moreover, the antitumor results showed that after heating, the Ni nanocomplex exhibited a substantial antitumor activity (IC₅₀ = 1.280 g/mL), which was higher than the activity of cis-platin (IC₅₀ = 1.714 g/mL). Finally, molecular-docking studies were performed to understand the evaluated compounds’ ability to bind to methionine adenosyl-transferases (PDB ID: 5A19) in liver cancer and COVID-19 main protease (PDB ID: 6lu7) cell-proteins. The findings reveal that [NiL₂]·1.5H₂O₂ has a higher binding energy of −37.5 kcal/mol with (PDB ID: 5A19) cell protein. Full article

The Schiff bases reaction is applied to form various functioned carbon structures using renewable carbon from waste sources, Chitosan, 4-Amino-3-hydroxy-napthalene-1-sulphnic acid, and dimethyl amino benzaldehyde as starting materials. The formed functioned carbons were characterized by TEM, FTIR, XRD, and surface area analysis to assess their morphology, structure, porosity, and surface functional groups. In addition, the chromatographic-based thermodynamic analysis is applied to evaluate the surface energy and thermodynamic parameters during the separation of hydrocarbon species. Results indicated the formation of various carbon structures in convex-like shapes with diameters between 600 nm and 1500 nm, including side-building edges of diameter between 100 nm and 316 nm. The formed functioned carbon surfaces are rich with O-H, N=C, C=C, C=O, and C=S groups, as indicated by the FTIR. The function carbons are named carbon coated with Chitosan-derived covalent organic layer (C@Chitosan-COL) as well as Schiff’s base-derived sulfonated carbon (Schiff’s-C-S) in relation to the applied starting materials. The chromatographic-based thermodynamic analysis showed that the entropy changes of adsorption (ΔS_A) increased with increasing chain length demonstrating less random movement and higher adsorption in both materials. The fabricated C@Chitosan-COL and Schiff’s-C-S showed an efficient separation of hydrocarbon mixture including n-Nonane, n-Decane, n-Undecane, and n-Dodecane. Full article

The condensation product of the reaction between aniline and salicylaldehyde was a 2-(2-hydroxybenzylidinemine)—aniline Schiff base bidentate ligand (L). L was used to generate complexes by interacting with the metal ions lanthanum(III), zirconium(IV), yttrium(III), and copper(II), in addition to cobalt(II). Various physicochemical techniques were utilized to analyze the synthesized L and its metal chelates, including elemental analysis (CHN), conductimetry (Λ), magnetic susceptibility investigations (μ_eff), Fourier-transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance (¹H NMR) spectroscopy, ultraviolet–visible (UV-Vis.) spectrophotometry, and thermal studies (TG/DTG). FT-IR revealed that the L molecule acted as a bidentate ligand by binding to metal ions via both the oxygen atom of the phenolic group in addition to the nitrogen atom of the azomethine group. Additionally, ¹H NMR data indicated the formation of complexes via the oxygen atom of the phenolic group. An octahedral geometrical structure for all of the chelates was proposed according to the UV-Vis. spectra and magnetic moment investigations. Thermal analysis provided insight into the pattern of L in addition to its chelates’ breakdown. In addition, the investigation furnished details on the chelates’ potential chemical formulas, the characteristics of adsorbed or lattice H₂O molecules, and the water that is coordinated but separated from the structure at temperatures exceeding 120 °C. The thermodynamic parameters utilizing Coats–Redfern in addition to Horowitz–Metzger equations were studied. The antimicrobial effectiveness of L and its chelates against distinct species of bacteria and fungi was studied using the disc diffusion method. Cu(II) and Y(III) chelates had significant antimicrobial activity against Staphylococcus aureus and Micrococcus luteus. Full article

This study presents a green protocol for the fabrication of a multifunctional smart nanobiocomposite (NBC) (ZnO-PIACSB-TiO₂) for secure antimicrobial and antibiofilm applications. First, shrimp shells were upgraded to a polyimidazolium amphiphilic chitosan Schiff base (PIACSB) through a series of physicochemical processes. After that, the PIACSB was used as an encapsulating and coating agent to manufacture a hybrid NBC in situ by co-encapsulating ZnONPs and TiO₂NPs. The physicochemical and visual characteristics of the new NBC were investigated by spectral, microscopic, electrical, and thermal methods. The antimicrobial indices revealed that the newly synthesized, PIACSB-coated TiO₂–ZnO nanocomposite is an exciting antibiotic due to its amazing antimicrobial activity (MIC/MBC→0.34/0.68 μg/mL, 0.20/0.40 μg/mL, and 0.15/0.30 μg/mL working against S. aureus, E. coli, and P. aeruginosa, respectively) and antifungal capabilities. Additionally, ZnO-PIACSB-TiO2 is a potential fighter of bacterial biofilms, with the results being superior to those of the positive control (Cipro), which worked against S. aureus (only 8.7% ± 1.9 biofilm growth), E. coli (only 1.4% ± 1.1 biofilm growth), and P. aeruginosa (only 0.85% ± 1.3 biofilm growth). Meanwhile, the NBC exhibits excellent biocompatibility, as evidenced by its IC₅₀ values against both L929 and HSF (135 and 143 µg/mL), which are significantly higher than those of the MIC doses (0.24–24.85 µg/mL) that work against all tested microbes, as well as the uncoated nanocomposite (IC₅₀ = 19.36 ± 2.04 and 23.48 ± 1.56 µg/mL). These findings imply that the new PIACSB-coated nanocomposite film may offer promising multifunctional food packaging additives to address the customer demand for safe, eco-friendly food products with outstanding antimicrobial and antibiofilm capabilities. Full article

A new chlorobenzylidene imine ligand, (E)-1-((5-chloro-2-hydroxybenzylidene)amino) naphthalen-2-ol (HL), and its [Zn(L)(NO₃)(H₂O)₃], [La(L)(NO₃)₂(H₂O)₂], [VO(L)(OC₂H₅)(H₂O)₂], [Cu(L)(NO₃)(H₂O)₃], and [Cr(L)(NO₃)₂(H₂O)₂], complexes were synthesized and characterized. The characterization involved elemental analysis, FT-IR, UV/Vis, NMR, mass spectra, molar conductance, and magnetic susceptibility measurements. The obtained data confirmed the octahedral geometrical structures of all metal complexes, while the [VO(L)(OC₂H₅)(H₂O)₂] complex exhibited a distorted square pyramidal structure. The complexes were found to be thermally stable based on their kinetic parameters determined using the Coats–Redfern method. The DFT/B3LYP technique was employed to calculate the optimized structures, energy gaps, and other important theoretical descriptors of the complexes. In vitro antibacterial assays were conducted to evaluate the complexes’ potential against pathogenic bacteria and fungi, comparing them to the free ligand. The compounds exhibited excellent fungicidal activity against Candida albicans ATCC: 10231 (C. albicans) and Aspergillus negar ATCC: 16404 (A. negar), with inhibition zones of HL, [Zn(L)(NO₃)(H₂O)₃], and [La(L)(NO₃)₂(H₂O)₂] three times higher than that of the Nystatin antibiotic. The DNA binding affinity of the metal complexes and their ligand was investigated using UV-visible, viscosity, and gel electrophoresis methods, suggesting an intercalative binding mode. The absorption studies yielded K_b values ranging from 4.40 × 10⁵ to 7.30 × 10⁵ M⁻¹, indicating high binding strength to DNA comparable to ethidium bromide (value 10⁷ M⁻¹). Additionally, the antioxidant activity of all complexes was measured and compared to vitamin C. The anti-inflammatory efficacy of the ligand and its metal complexes was evaluated, revealing that [Cu(L)(NO₃)(H₂O)₃] exhibited the most effective activity compared to ibuprofen. Molecular docking studies were conducted to explore the binding nature and affinity of the synthesized compounds with the receptor of Candida albicans oxidoreductase/oxidoreductase INHIBITOR (PDB ID: 5V5Z). Overall, the combined findings of this work demonstrate the potential of these new compounds as efficient fungicidal and anti-inflammatory agents. Furthermore, the photocatalytic effect of the Cu(II) Schiff base complex/GO was examined. Full article