Oxidative Polymerization Research Articles

Stearic Acid as Polymerization Medium, Dopant and Hydrophobizer: Chemical Oxidative Polymerization of Pyrrole.

In recent years, fatty acids have garnered significant attention as a natural phase-change material and a hydrophobizer due to their biocompatibility and biodegradability. In this study, the utilization of fatty acid is proposed as a polymerization medium for the first time. As a specific reaction, chemical oxidative polymerizations of pyrrole is conducted using ferric chloride as an oxidant in a stearic acid medium. The polymerizations resulted in the production of micrometer-sized polypyrrole (PPy) grains, which are aggregates of atypical primary particles with submicrometer size. The PPy grains are doped with stearic acid, suggesting that the stearic acid functioned as a dopant and a hydrophobizing agent as well as a polymerization medium. The dried PPy grains can adsorb at the air-water interface and function as a liquid marble stabilizer with light-to-heat photothermal properties. The liquid marble can move on a planar air-water interface by Marangoni flow induced by NIR laser light irradiation.

Investigation of functionalized graphene oxide incorporated superabsorbent polymers for enhanced durability, hydration, microstructure and mechanical strength of modified concrete

ABSTRACT This study focuses on enhancing cementitious materials by incorporating silanized graphene oxide (SGO) and superabsorbent polymers (SAPs), aiming to improve their mechanical and durability properties. The primary goal is to evaluate the effects of SGO/SAP composites on the hydration, absorption, shrinkage, and overall performance of concrete. The composites were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) to understand their microstructure. Mechanical and durability tests revealed that adding SGO/SAP composites significantly increased the mechanical strength and water absorption capabilities of the concrete. The compressive strength, split tensile strength, and flexural strength of the SGO/SAP-modified concrete were measured at 57 MPa, 4.90 MPa, and 8.25 MPa, respectively. Shrinkage tests demonstrated the composite hydrogel’s excellent water-holding capacity at 0.3 wt.% SGO/SAP, facilitating internal curing in concrete structures. FE-SEM analysis indicated a reduction in microcracks due to the presence of SGO/SAP. The improvements are attributed to the synergistic effects of SGO and SAP, which enhance water retention, dispersion, and interfacial bonding within the cementitious matrix. The microstructural studies confirmed the exceptional stability of the SGO/SAP-modified mix, emphasizing its potential as an additive to improve concrete properties. This research underscores the significant potential of SGO and SAP in advancing the performance of cement-based materials, highlighting their applicability in infrastructure development and construction for creating more durable and high-performing concrete structures.

“Click”able monomer and polymers based on Azide-functionalized 3,4-Propylenedioxythiophene with tunable processibility

This research introduces 3,3-bis(azidomethyl)-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine (ProDOT-AM2) as a versatile building block monomer for the synthesis of variously functionalized monomers and copolymers via “click”able 1,3-dipolar cycloaddition. The efficiency of this building block as a precursor to a wide range of ProDOT-based monomers is demonstrated by click reaction with various alkynes. The 1,3-dipolar cycloaddition of ProDOT-AM2 with different alkynes in the presence of a catalyst yields a novel class of ProDOT derivatives via a “triazole-locker” mechanism. Depending on the bases utilized, two distinct types of functionalized monomers, namely bistriazole and triazole, are obtained. The resulting polymers from the oxidative polymerization of selected monomers exhibit high solution processability and stability under multiple chemical redox processes, demonstrating potential applications in chemical chromics. Additionally, a conjugated copolymer containing ProDOT-AM2 is synthesized via Stille reaction conditions and subsequently post-functionalized with alkynes via a “triazole-locker” mechanism. Characterization studies via IR and 1H NMR confirm the successful post-functionalization of the polymer. Electropolymerization of ProDOT-AM2 yields an electroactive polymer (PProDOT-AM2), indicating its potential utility in conducting polymers to be further post-functionalized. Overall, this methodology presents a straightforward approach for synthesizing a new class of monomers for conducting polymers and polymer modification using click chemistry.

Synergistic adsorption–photocatalytic degradation of the emerging contaminant hydroxybenzotriazole by a 3D sponge-like easy separation polypyrrole/TiO2 composite

Herein, a 3D sponge-like polypyrrole/TiO2 (Ppy-TiO2) composite aerogel was developed for the first time to remove hydroxybenzotriazole (HOBt) from water. Mesoporous TiO2 was prepared via a sol–gel method, and then the Ppy-TiO2 composite hydrogel was prepared by oxidative polymerization and converted to aerogel by freeze-drying. The morphological, compositional, and surface characteristics of the prepared materials were detailly characterized. The characterization studies revealed that pure anatase mesoporous TiO2 nanoparticles were successfully prepared and incorporated into amorphous 3D Ppy with a porous chain-like network structure. Coupling Ppy and TiO2 extended the light absorption to the visible region and decreased the electron/hole recombination rate. The performance studies revealed that the Ppy-TiO2 composite has higher adsorption and photocatalytic activities than the sum of the individual components. Optimum performance was obtained at pH 5.3 using 0.25 g/L of the Ppy-TiO2 composite with a Ppy: TiO2 mass ratio of 1:1. The intermolecular hydrogen bonding was pivotal in the adsorption process which was multilayer. The degradation of HOBt occurs primarily by holes, then superoxide anion radicals. The total organic carbon (TOC) analysis showed a 90% reduction in carbon content after 30 min of treatment. The toxicity study indicated that the photocatalytic process decreased the toxicity of the HOBt solution. The synergism between adsorption and photocatalysis, easy separation, and reusability promote the application of Ppy-TiO2 composite aerogel for water treatment.

Metal Ions Modified Azo‐Linked Porous Polymers for High Performance CO2 Capture

AbstractPorous polymer show great potential for CO2 capture owing to its high specific surface area, adjustable porous structure and chemical structure. Herein, a novel CO2 adsorption materials ALP−M (M: Cu2+, Mg2+, Ni2+) were prepared through coordination between azo‐linked porous polymer (ALP) synthesized by oxidative coupling polymerization of tris(4‐aminophenyl)amine and metal ions. The structures and morphology of as‐prepared materials were demonstrated by FT‐IR, XRD, XPS, BET and SEM, the CO2 capture performance and mechanism of ALP−M were also investigated through static adsorption and column adsorption experments, the results show that metal ions can enhance the CO2 adsorption and desorption performance of ALPs by coordination adsorption. ALP−M showed a highest static CO2 adsorption capacity of 2.67 mmol g−1 at 273 K (1 bar), which is 35.5 % higher than that of ALP. The metal ions served as Lewis acid sites can enhance the affinity of adsorbent for CO2. In column adsorption experiments, the ALP−M showed a higher saturated adsorption capacity 4.99 mmol g−1 at 273 K (1 bar) than that of static adsorption, and excellent cycling stability after 500 adsorption and desorption cycles, the adsorption capacity retention rate of ALP−M for CO2 can reach 98 %.

Novel Ag-Doped- Poly (aniline-co-pyrrole)/Titanium-Dioxide Nanocomposite Sensor Material for Ammonia Detection in Spoiled Meat

Silver-doped poly(aniline-co-pyrrole)/titanium dioxide (Ag-doped PANI-PPy/TiO2) conducting copolymer-based nanocomposite ammonia gas sensor was synthesized through in situ chemical oxidative polymerization by taking different amounts (4%, 5%, 6%, 7%, and 8%) of Ag-TiO2 (1:1 ratio) nanoparticles. Zetasizer; dynamic light scattering, scanning electron microscopy, transmit ion electron microscopy, Fourier transform infrared, X-ray diffraction, UV–vis spectroscopy, differential scanning calorimetry, thermogravimetric analysis, and cyclic voltammetry characterization techniques were used to confirm the real formation of nanocomposites and to evaluate the detection performance of the sensor. The interaction sensitivity of the synthesized nanocomposite sensor with ammonia (NH3) was determined by changing the amounts of nanoparticles. Spectroscopic determination exhibited excellent porosity and a better shift in the absorption bands having band gaps (1.87 eV) for the Ag-doped PANI-PPy/TiO2 nanocomposite sensor than the PANI-PPy copolymer (3.17 eV). Morphological (10 μm) and nanoparticle arrangement studies (20 μm) have shown the uniform allocation of nanoparticles in the copolymer matrix when 6% of Ag-TiO2 (1:1 ratio) was added, while agglomeration occurred when <6% or >6% of Ag-TiO2 was added to the copolymer. A decrease in the amorphous domain of the copolymer with an increase in nanoparticles was observed from the X-ray diffraction and other results.

Detection of tetracycline by molecularly imprinted electrochemical sensor based on the modification of poly(3,4-propylene dioxythiophene)/chitosan/au

In this study, a molecularly imprinted polymer (MIP) electrochemical sensor based on poly(3,4-propylenedioxythiophene)/chitosan/Au (PProDOT/CS/Au) composite modification was designed for highly sensitive and selective detection of TC. Green synthesis of CS/Au without the use of reducing agents, followed by in-situ oxidation polymerization of PProDOT. The high electrochemical activity and high stability of PProDOT, the numerous functional groups (-OH, -NH2) of CS, and the excellent electron transport capacity of AuNPs, which provided a suitable incubation chamber for the production of imprinted cavities. Meanwhile, combined with the specific recognition ability of MIP, it showed superior performance over bare glassy carbon electrodes. Under the optimal experimental conditions, this sensor showed good linearity for TC in the concentration ranges of 0.0001–100 μM, with a low limit of detection (LOD) of 0.19 nM. At the same time, the sensor exhibited satisfactory selectivity, repeatability, reproducibility and stability. It was evident from the results of the study that the sensor designed in this paper showed considerable potential for application in the detection of TC in pharmaceuticals, the environment, and food samples.

Fabrication of core–shell nickel ferrite@polypyrrole composite for broadband and efficient electromagnetic wave absorption

Herein, nickel ferrite@polypyrrole (NiFe2O4@PPy) composite was prepared by a simple two-step route of solvothermal synthesis and in-situ oxidation polymerization reaction. The results of micromorphology analysis showed that the obtained NiFe2O4@PPy composite had a unique core–shell structure, good magnetic performance and electrical conductivity. Furthermore, the as-prepared magnetic/conductive NiFe2O4@PPy composite exhibited notably enhanced electromagnetic wave (EMW) absorption performance than pure NiFe2O4 and PPy. When the filling ratio was 17.5 wt% and the matching thickness was 2.24 mm, the optimal minimum reflection loss (RLmin) of −56.25 dB and a broad effective absorption bandwidth (EAB) of 5.2 GHz were achieved for NiFe2O4@PPy composite. With slightly increasing the matching thickness to 2.6 mm, the maximum EAB of 7.12 GHz could be reached. Additionally, the probable EMW absorption mechanism was elucidated. Therefore, this work could provide a valuable reference for the preparation of magnetic ferrite/conductive polymer composites as broadband and high-efficiency EMW absorbers.

Bifunctional PAni@Bi/Ce metal organic framework-Chitosan composite for electrochemical sensing and energy storage applications

Tailoring pristine metal-organic frameworks (MOFs) offered a great opportunity in exploring electrochemical sensing and energy storage applications. This study presents a novel Polyaniline@Bi/Ce MOF-Chitosan composite synthesized via a solvothermal method and chemical oxidative polymerization. PXRD, FTIR, SEM, EDAX, and TEM characterization confirmed its structural and morphological properties. Electrochemical performance was evaluated using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and electrochemical surface area (ECSA) analysis. The composite exhibited excellent electrocatalytic activity for detecting azithromycin and toluene with low detection limits and broad concentration ranges, demonstrated by voltammetry and amperometry. It showed significant stability for long term applications. Additionally, the material's energy storage capabilities were assessed through CV and galvanostatic charge-discharge (GCD) studies, revealing a specific capacitance of 415.32 F/g at 1.0 A g-1 and 90.48 % capacity retention after 5000 cycles at 6 A g-1. These findings highlight the Polyaniline@Bi/Ce MOF-Chitosan composite as a promising candidate for electrochemical sensing and energy storage applications.

Optical parameters of PANI.CSA/PMMA nanofibers

Abstract Polyaniline doped with camphor sulphonic/Poly(methyl methacrylate) PANI.CSA/PMMA nanofibers were manufactured by electrospinning technology, where all parameters of the electrospinning system are fixed and the effect of the needle gauge on the properties of the prepared nanofibers is studied at different needle gauge (18, 20, 23 G). The polyaniline was manufactured by aniline-chemical oxidation polymerization. The nanofibers were diagnosed by an FE-SEM scanner to identify the surface morphology of the samples and the diameters of the nanofibers, it shows that nanofibers become more regular and their diameters become smaller as the diameter of the needle decreases. The samples were measured by the analysis of UV-visible spectroscopy, identifying the optical properties of the nanofibers and calculating the energy gap, which was valued ranging from 2.8 eV to 3.2 eV, increased due to the phenomenon of the quantitative restriction. Absorption coefficient and optical constants were also studied as a function of needle gauge.

Fabrication of versatile and durable superhydrophobic cotton fabrics using PTA-Ala adhesive

In recent years, the preparation of functional textiles based on polyphenols adhesion has received extensive attention and research. However, polyphenols are prone to peroxidation during oxidative polymerization, which can compromise the interfacial adhesion of their monomers. Reintroducing reactive functional groups after oxidative polymerization of polyphenols may potentially compensate for the lost interfacial adhesion while increasing cohesion. In this paper, L-alanine (Ala) is introduced into poly (tannic acid) (PTA) solution to generate the PTA-Ala via Michael addition and Schiff base reaction. Original cotton fabrics are modified with PTA-Ala solution to enhance adhesion strength between the fabrics and subsequent functional modifiers. A silver nanowire network is then incorporated to increase the surface roughness through tannic acid reduction. Finally, polydimethylsiloxane is applied to reduce fabric surface energy, resulting in superhydrophobic multifunctional OH-PDMS/Ag/PTA-Ala/cotton fabrics. The finished cotton fabric exhibits a water contact angle of 166.7 ± 1.9° and a rolling angle of 5 ± 0.5°. Moreover, the fabric features diverse functionalities such as oil-water separation, photothermal conversion, antimicrobial properties, water collection, and anti-icing capabilities, alongside excellent durability and self-healing properties that extend its service life. This finished cotton fabric demonstrates promising applications in oil pollution control, outdoor clothing and medical protection, highlighting its broad across various industries.

Co-delivery of novel valsartan and hydrochlorothiazide pH-responsive electrospun polymeric nanofibers for improved oral delivery

Valsartan (VAL) and Hydrochlorothiazide (HCTZ) as a fixed-dose combination are widely used for the management of hypertension. To enhance the dissolution and oral delivery of VAL (BCS class II drug) and HCTZ (BCS class IV drug), nanofibers containing both drugs were prepared using an electrospinning technique. VAL/HCTZ-loaded NFs were prepared using Eudragit L100-55 (EUD L100-55) and Poly (ethyne oxide) (PEO) polymer mixture and the formulation process was optimized through three process variables of polymer composition, polymer concentration, and spinning voltage. VAL/HCTZ-loaded NFs were characterized for their size, surface morphology, entrapment efficiency (%EE), drug-polymer interaction, in vitro drug release, ex-vivo permeation, and in vivo studies. Smooth, beadles and uniform drug-loaded NFs were successfully fabricated using optimum polymer composition (EUD L100-55/PEO 3:1), concentration (12 % w/v), and applied voltage (30 KV). The optimum formula (F9) showed a low average nanosize of 300 nm and a high drug loading of > 90 % was achieved. In vitro, release results showed a pH-dependent drug release, with minimum drug released at pH lower than 4.5, but a significant and complete release of both drugs was achieved at pH 6.5. The EUD L100-55/PEO improved the dissolution of VAL and HCTZ compared to free drugs at the intestinal site of absorption. Differential Scanning calorimetry and Fourier Transform Infra-Red studies showed both drugs’ amorphization and compatibility between drugs and polymers. Permeability behavior for the VAL/HCTZ-loaded NFs was found to be significantly higher than free drug suspensions of both drugs which indicated the improvement of VAL and HCTZ permeability through the intestinal membrane. The in vivo study proved the enhanced oral anti-hypertensive action of drugs-loaded NFs compared to free drug suspensions. The superior in vitro release, ex-vivo permeation, and in vivo anti-hypertensive effect indicate that drug-loaded nanofibers have the potential to improve the biological activity and hence oral delivery of the fixed-drug combination.

Optimization and Characteristics of Multimodal Binder on Polymer Nanocomposite for Lightweight Applications

The process of selecting binders is complex because it requires finding a balance between improving material performance and reducing environmental impact. This involves challenges such as achieving nanoparticle dispersion, optimizing binder compatibility, and addressing environmental concerns. The main objective of this research on use the multimodal binder optimization characterization model (M-MBOCM) analysis to understand the intricate relationship between metal oxide nanoparticles, polymer matrices, and binders. These specialized nanocomposites have a wide range of potential applications. By intelligently selecting Scanning Characterization binders (SCB), industries can enhance material properties to meet specific requirements. This applies across various fields, from high-capacity energy storage devices to lightweight structural materials and smart sensors. This research involves analyzing metal oxide nanoparticle mage polymer nanocomposites with aqueous and nonaqueous binders in manganese dioxide-based cathodes (M-BC), hybrid supercapacitors (HS), and non-enzymatic glucose sensors (NEGS). The significance of M-BC in the present investigation results is based on advanced M-MBOCM and SCB techniques. The performance analysis ratio exceeds 95%, which is higher than the reported results for M-BC, HS, and NEGS. The scalability analysis ratio for M-MBOCM and SCM is observed to be higher than others, recorded at 93% and 88% respectively. These findings demonstrate the potential for enhanced nanocomposite materials in practical applications (lightweight) and drive their development.

Sulfur/reduced graphite oxide and dual-anion solid polymer‒electrolyte integrated structure for high-loading practical all-solid-state lithium–sulfur batteries

The demand for high-capacity batteries with long cycle life and safety has been increasing owing to the expanding mid-to-large battery market. Li–S batteries are suitable energy-storage devices because of their reversibility, high theoretical capacity, and inexpensive construction materials. However, their performance is limited by various factors, including the shuttle effect and dendrite growth at the anode. Here, an integrated electrode for use in all-solid-state (ASS) Li–S batteries was formed via hot pressing. In detail, S particles dispersed in a functionalized reduced graphite oxide (rGO) cathode with a binder-less polymer electrolyte (PE) and a dual-anion ionic liquid-containing cross-linked poly(ethylene oxide)–Li bis(fluoromethanesulfonyl)imide–N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide-based solid polymer electrolyte (SPE, PEO–LiFSI0.1(Pyr14TFSI)0.4) were hot-pressed into an integrated electrode, which serves as both the cathode and electrolyte. The resulting S/rGO-based solid-state Li–S batteries exhibited more stable performance than Li–S batteries using liquid electrolytes did, indicating that the dual-anion SPE layer effectively suppressed dendritic Li formation and the shuttle effect with high ionic conductivity. At 0.1 C, the battery discharge capacities were 957 and 576 mAh g−1 in the first cycle and after 100 cycles, respectively. At 1 C, the reversible capacity was 590 and 417 mAh g−1 in the first cycle and after 100 cycles, respectively (capacity retention = 71%). Therefore, the proposed S/rGO/PE//LiFSI0.1(Pyr14TFSI)0.4-integrated electrodes are beneficial for ASS Li–S batteries.

Urushiol oligomer preparation and evaluations of their antibacterial, antioxidant, and thermal stability

There have been studies published on the composition and coating uses of raw lacquers following enzymatic oxidative polymerization. The change of urushiol’ thermal stability and biological activity following polymerization to create oligomer, however, has received little attention. This work using silica gel column chromatography to separate urushiol and urushiol oligomer from polymerized raw lacquer and assessed its antibacterial, antioxidant, and thermal stability in an effort to decrease the allergenicity of urushiol and increase its application. By using gel chromatography, the urushiol oligomer were discovered to be polymers with 2–5 degrees of polymerization. According to characterization results from techniques like UV, FT-IR, and 1H NMR, urushiol was converted into urushiol oligomer by addition reactions, and C–C coupling. The findings demonstrated that the urushiol oligomer’ IC50 values for scavenging DPPH and ABTS free radicals were 40.8 and 27.4 μg/mL, respectively, and that their minimum inhibitory concentrations against Staphylococcus aureus and Staphylococcus epidermidis were 250 and 125 μg/mL. The urushiol oligomer’s thermogravimetric differential curve peak temperature (461.8 °C) was higher than urushiol’s (239.5 °C), indicating that urushiol undergoes polymerization with enhanced thermal stability. The study’s findings establish a foundation for the use of polymerized urushiol and urushiol oligomer in applications including functional materials and additives.

MXene-based self-adhesive, ultrasensitive, highly tough flexible hydrogel pressure sensors for motion monitoring and robotic tactile sensing

With the rapid development of artificial intelligence and human–computer interaction fields, wearable electronic devices represented by flexible pressure sensors have a wider range of application scenarios. In this paper, we used a composite hydrogel made by one-pot polymerization using a combination of acrylamide (AM), sodium carboxymethyl cellulose (CMC), dopamine (DA), and MXene (Ti3C2Tx). The composite hydrogel has the advantages of self-adhesion, high sensitivity, large detection range (0–500 kPa), low detection limit, high toughness (compression > 90 %), stability (more than 6700 s) and other advantages of hydrogel flexible pressure strain sensor. Sodium carboxymethyl cellulose (CMC), as a multifunctional thickener and gelling agent, significantly improves rheological properties and viscosity in hydrogels, forms crosslinked structures to enhance mechanical properties and provides reliable toughness for pressure sensors. Dopamine (DA), which is rich in catechol groups, can adhere to the material surface through oxidative polymerization to enhance bond strength. Hydrogel pressure sensors for human motion detection can accurately track joint movement, respond sensitively to changes in knocks and touches, and display specific characters such as Morse code. The technology extends to robotic systems, where pressure-activated electrical signals are used to control robot movements. Therefore, it has a very promising application in the field of human–computer interaction, human-body movement signal detection, etc. PAM/CMC/DA/MXene hydrogel pressure sensors have excellent mechanical, electrical, and adhesion properties, which provide a more reliable solution for the fields of flexible wearable e-skin, human–computer interaction, and tactile sensing.

Self-Polymerized Tough and High-Entanglement Zwitterionic Functional Hydrogels.

Zwitterionic hydrogels exhibit great potential in biomedical applications due to their antifouling properties and biocompatibility. However, the single-network structure of pure zwitterionic hydrogels leads to a low toughness and strength, limiting their application in biomedical fields. In this work, a high entanglement sulfobetaine methacrylate-dopamine hydrogel (SBMA-DA-PE) with low cross-linker content and high monomer concentration is prepared by using a dopamine oxidative radical polymerization method. Compared to a regular zwitterionic hydrogel, the SBMA-DA-PE hydrogel exhibits a 5-fold increase in tensile fracture stress and a 10-fold increase in compressive fracture stress. The SBMA-DA-PE hydrogel possesses excellent mechanical properties (the maximum compressive stress ≥4.85MPa, the maximum compressive strain ≥90%). Besides, the non-covalent interactions between catechol or ortho-quinones within the SBMA-DA-PE hydrogel, combined with strong intermolecular electrostatic interactions, endow the SBMA-DA-PE hydrogel with great self-healing capabilities and fatigue resistance. The SBMA-DA-PE hydrogel demonstrates low swellability and possesses good antifouling properties. Furthermore, the good printability and conductivity of the tough SBMA-DA-PE hydrogel endows it with new possibilities for developing biological 3D scaffolds and electronic devices. Overall, this work provides new insights into the preparation of zwitterionic hydrogels with high mechanical strength and multi-functionality for biomedical applications.

Magnetic Nanocomposites Revolutionize Heavy Metal Adsorption for Environmental Cleanup

General background: Magnetic nanocomposites have garnered significant attention due to their multifunctional properties, particularly in environmental remediation, where they can be used for the removal of heavy metals from aqueous solutions. Specific background: Polypyrrole (PPy) and poly(p-hydroxyaniline) (P(p-OH An)) are conductive polymers known for their adsorption capabilities, while Fe3O4 nanoparticles exhibit magnetic properties, facilitating separation and recovery. Knowledge gap: Despite the potential of Fe3O4-based composites, few studies have systematically explored the synergistic adsorption properties of PPy and P(p-OH An) in Fe3O4-based nanocomposites under varying environmental conditions. Aims: This study aimed to synthesize and characterize Fe3O4/PPy/P(p-OH An) magnetic nanocomposites and evaluate their adsorption performance under different temperatures and isotherm models. Results: The nanocomposite was synthesized through chemical oxidation polymerization and characterized using FTIR, TEM, AFM, and TGA, confirming its successful formation and nanoscale structure. Adsorption studies indicated an exothermic process, with a decrease in adsorption capacity at higher temperatures. The adsorption data fit the Freundlich isotherm better than the Langmuir model, suggesting heterogeneous surface adsorption. Novelty: This study demonstrates a novel Fe3O4/PPy/P(p-OH An) nanocomposite with superior adsorption properties, showing its potential in heavy metal ion removal and offering an improved understanding of temperature effects on adsorption performance. Implications: The findings underscore the composite's promise for environmental remediation applications, particularly in water treatment, and suggest further optimization of the adsorption conditions and evaluation of the composite's reusability for industrial-scale applications. Highlights: Enhanced Adsorption: Fe3O4/PPy nanocomposites offer combined magnetic and polymer adsorption properties. Temperature Sensitivity: Adsorption decreases as temperature rises, indicating exothermic behavior. Surface Interaction: Freundlich isotherm shows adsorption occurs on heterogeneous surfaces. Keywords: Magnetic nanocomposite, Fe3O4, Polypyrrole, Adsorption, Environmental remediation.

Achieving a high‐performance anti‐corrosive polyvinyl ester based on bisphenol a coating by addition of polyaniline‐Cu‐based metal organic framework composite

AbstractCorrosion of steel is one of the challenging issues that researchers has focused on it. Among corrosion control methods, organic coatings with suitable lifetime and efficiency are a great of interest. In the present research, polyaniline‐ copper‐based metal organic framework (PANI‐Cu‐MOF) is synthesized using in‐situ oxidation polymerization method and successfully characterized with different techniques. Then, 0.5, 1, and 1.5 wt. % of PANI‐Cu‐MOF composite are added to vinyl ester (VE) resin based on bisphenol A and coated on ST37 steel. The performance of the as‐prepared coatings on ST37 is evaluated using electrochemical impedance spectroscopy (EIS) for 360 h. The EIS results showed that loading of PANI‐Cu‐MOF (0.5 wt. %) in VE led to the highest protective properties against aggressive species with |Z|0.01 Hz = 6.76 × 107 Ωcm2 after 360 h. The uniform distribution of PANI‐Cu‐MOF composite in VE and its hydrophobic property causes a delay in the penetration of the corrosive species into the coating, thus increasing the corrosion resistance.Highlights PANI‐Cu‐MOF composite is embedded to VE resin as novel anti‐corrosive pigment. The highest Rcoat are achieved for VE‐PANI‐Cu‐MOF 0.5 wt. %. In the presence of PANI‐Cu‐MOF, the corrosive species penetrations decreased.

New spacious SrWO4/PEDOT-PPy nanohybrids and their electrochemical and photocatalytic activities.

A novel SrWO4-poly(3,4-ethylene dioxythiophene) (PEDOT)-polypyrrole (PPy) nanocomposite was synthesized via chemically oxidative polymerization and considered by using numerous method of the techniques. The resulting SrWO4/PEDOT-PPy nanocomposite demonstrated remarkable electrochemical sensing capabilities for sulfadiazine (SFA). As a modified glassy carbon electrode (SrWO4/PEDOT-PPy/GCE) revealed for superior catalytic activity in the electrochemical oxidation of sulfadiazine, enabling sensitive detection with quantification and detection limits of 1.0936 × 10-9M µA-1 and 2.2104 × 10-9M µA-1, respectively. This technique effectively determined SFA content in real samples. Additionally, SrWO4/PEDOT-PPy demonstrated extraordinary photocatalytic ability, achieving a Methylene Blue (MB) degradation rate of up to 99.1% under halogen light irradiation within 80min. Hybrid photocatalyst has exhibited to strong reusability and photocatalytic stability under frequent light exposure. A contrivance for the photocatalytic deprivation of MB by SrWO4/PEDOT-PPy is proposed. These results underscore the crucial role of SrWO4/PEDOT-PPy in practical environmental remediation analysis. The fluorescence investigations have betrothed to terephthalic acid radical formations of SrWO4/PEDOT-PPy hybrids, which were modulated by different approaches, and its mainly driven for higher illumination aptitudes. Meanwhile, this was more supporting for physio-chemical properties of the phenomenon, at this consequential with significantly well improved to the photocatalytic performances. Because of this, SrWO4/PEDOT-PPy hybrid materials were comprehended to deliver excellent kinetics, and better recyclable activities.