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This work aimed to develop a simple, very stable, and sensitive biosensor to detect methadone for athlete doping monitoring by integrating polyaniline and graphitic carbon nitride on a glassy carbon electrode (PANI/g-C3N4/GCE). Using modified g-C3N4/GCE, the deposition approach was used to electrooxidize and polymerize aniline. The electrodeposited and polymerized aniline particles on g-C3N4 surfaces were confirmed by the structural analysis results. The addition of g-C3N4 to PANI produced a network film that improved stability and sensitivity and significantly increased electron mobility, according to cyclic-voltammetry and differential-pulse-voltammetry measurements. The DPV responses of PANI/g-C3N4/GCE indicated that this methadone sensor has sensitivity of 0.0891 μA/μM, linear-range of 1–520 μM, and detection limit of 4 nM. In this study, the proposed sensor's methadone detection capabilities were tested using prepared urine samples from four young athletes, ages 26–32. The sensor's accuracy and dependability are demonstrated by the significant recovery values (more than 97.00 %), suitable precision (RSD less than 4.69 %), and agreement between measurements made using the DPV and the methadone test kit. These findings demonstrate the developed sensor's potential to improve athletes' doping control by offering a dependable methadone detection technique.

Abstract This work reports the electrochemical fabrication of thin films comprising polyaniline nanofibers (PANI) in conjunction with graphene oxide (GO) and reduced graphene oxide (rGO) on ITO substrate, along with examining the electrochemical properties, with a focus on the influence of the substrate and electrolyte in the electrodeposition methods. The study explores the electrochemical characteristics of these thin films and establishes a flexible framework for their application in diverse sectors such as sensors, supercapacitors, and electronic devices. It analyzes the impact of the substrate and electrolyte in electrodeposition techniques. The effects were studied using techniques such as cyclic voltammetry and chronoamperometry. The fabrication process of PANI/GO and PANI/rGO thin films involved the integration of rGO within PANI via electropolymerization, conducted under sulfuric acid. GO was synthesized by modifying the well-known Hummers’ method and characterized by X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). SEM showed the diameters of the formed PANI were between 40 and 150 nm, which helped to intertwine the rGO nanosheets with PANI nanofibers to form thin films. The electrochemical behavior of the PANI/rGO thin films was examined using cyclic voltammetry (CV) and chronoamperometry in different electrolytes, including sulfuric acid (H₂SO₄) and potassium nitrate (KNO₃). The CV profiles exhibited distinct oxidation and reduction peaks, with variations in the voltammogram morphology attributed to the nature of the electrolyte and the substrate employed during the electrodeposition process. These results highlight the critical role of both the substrate and electrolyte in governing the electrochemical performance of PANI/rGO thin films. The findings from this study demonstrate a versatile approach for the fabrication of PANI/graphene-based thin films with tunable electrochemical properties, and such a strategy has great application to fabricating other thin film composites for supercapacitors or other control source frameworks requiring enhanced charge storage and electrochemical responsiveness.

Abstract Present work reports solution combustion synthesis (SCS) of Co0.5Zn0.5Fe2O4 spinel ferrite, its chemical modification with polymethylmethacrylate (PMMA), synthesis of polyaniline (PANI), and electromagnetic interference (EMI) shielding properties of their composites. Both as-prepared and PMMA-modified Co0.5Zn0.5Fe2O4 adopt cubic spinel structure as shown by X-ray diffraction studies. Field emission scanning electron microscopy images show the agglomerated and microporous nature of the ferrites. High resolution transmission electron microscopy image of as-prepared Co0.5Zn0.5Fe2O4 shows lattice fringes related to (311) plane of the spinel structure. X-ray photoelectron spectroscopy studies reveal the presence of Co2+, Zn2+, and Fe3+ in tetrahedral and octahedral coordinations in the ferrite. EMI shielding properties are evaluated for PMMA-modified Co0.5Zn0.5Fe2O4 and PANI composites in different weight ratios. Composites containing PMMA-modified ferrite and PANI with 50:50 and 10:90 weight ratios show the best performance among all the composites in 2−20 GHz frequency range. Optimized PMMA-modified Co0.5Zn0.5Fe2O4 and PANI composite with the ratio of 10:90 shows shielding effectiveness (SE) values of −16.6 to −24.2 dB in 2−20 GHz frequency region. Graphical Abstract

Abstract Three types of synthetic coal-derived adsorbents were characterized as potential enhanced structurers during the removal of chlorpyrifos pesticide. The raw coal (CA) was activated into porous graphitic carbon (AC), and both CA and AC were blended with polyaniline polymers (PANI/CA and PANI/AC) forming two advanced composites. The adsorption performances of the modified structures in comparison with CA were evaluated based on both the steric and energetic parameters of the applied advanced isotherm model (the monolayer model of one energy). The uptake performances reflected higher capacities for the PANI hybridized form (235.8 mg/g (PANI/CA) and 309.75 mg/g (PANI/AC) as compared to AC (156.9 mg/g) and raw coal (135.8 mg/g). This signifies the impact of activation step and PANI blending on the surface and textural properties of coal. The steric investigation determined the saturation of the coal surface with extra active sites after the activation step (Nm(AC) = 62.05 mg/g) and the PANI integration (Nm(PANI/CA) = 113.5 mg/g and Nm(PANI/AC) = 169.7 mg/g) as compared to raw coal (Nm(CA) = 39.6 mg/g). This illustrated the reported uptake efficiencies of the modified samples, which can be attributed to the enhancement in the surface area and the incorporation of additional chemical groups. The results also reflect that each site can be loaded with 3–4 molecules of chlorpyrifos, which are arranged vertically and adsorbed by multi-molecular mechanisms. The energetic studies (

A set of Pd-containing composites was prepared by the deposition of Pd on the following carriers: polyaniline (PANI); PANI doped by H2SO4; Norit GSX activated carbon or Aerosil (SiO2) coated by PANI or by H2SO4-doped PANI; PANI after thermal treatment at 300 °C in an atmosphere of H2. One sample was also prepared by the in situ polymerization of aniline in the presence of Pd2+· The decomposition of Pd was carried out via deposition from the solutions of Pd2+ salts or decomposition of Pd0 complex Pd2(dba)3, where dba is dibenzylideneacetone. The composites were studied by powder X-ray diffraction, transmission electron microscopy, IR and Raman spectroscopy. The hydrogenation of quinoline in the presence of composites was carried out; the catalytic performance of the composites was evaluated by the yield of 1,2,3,4-tetrahydroquinoline. It was found that the doping of PANI by H2SO4, inclusion of Norit GSX activated carbon as a component of the carrier or thermal treatment of PANI prior to the deposition of Pd led to significant increase in the catalytic performance of the composites in the hydrogenation of quinoline.

The search for new green and efficient stabilizers is of great importance for the stabilization of nitrocellulose (NC). This is due to the shortcomings of traditional stabilizers, such as high toxicity. In this study, reduced polyaniline (r-PANI), which has a similar functional structure to diphenylamine (DPA) but is non-toxic, was prepared from PANI based on the action with N2H4 and NH3–H2O, and used for the first time as a potential stabilizer for NC. XPS, FTIR, Raman, and SEM were used to characterize the reduced chemical structure and surface morphology of r-PANI. In addition, the effect of r-PANI on the stabilization of NC was characterized using DSC, VST, isothermal TG, and MMC. Thermal weight loss was reduced by 83% and 68% and gas pressure release by 75% and 49% compared to pure NC and NC&3%DPA, respectively. FTIR and XPS were used to characterize the structural changes of r-PANI before and after reaction with NO2. The 1535 cm−1 and 1341 cm−1 of the FTIR and the 404.98 eV and 406.05 eV of the XPS showed that the –NO2 was generated by the absorption of NO2. Furthermore, the quantum chemical calculation showed that NO2 was directly immobilized on r-PANI by forming –NO2 in the neighboring position of the benzene ring.

Abstract Conductive polymer nanocomposites for electromagnetic interference (EMI) shielding are important materials that can be combat the increasingly dangerous radiation pollution arising from electronic equipment and our surrounding environment. In this work, we have synthesized polyaniline-copper nanoparticles (PANI-Cu NPs) by the copper salt based oxidative polymerization method at room temperature and then added with different concentration (0, 1, 3 and 5 wt%) in polystyrene polymer forming PS/ PANI-Cu nanocomposites films by means of the traditional solution casting technique. The formed PANI-Cu NPs were investigated by UV/Vis spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM) and SEM/EDX elemental mapping techniques. On the other hand, the prepared PS/PANI-Cu nanocomposites films were evaluated by UV and SEM, the mechanical properties of the nanocomposites films were evaluated and showed an improvement by added PANI-Cu NPs up to 3 wt% and 50 kGy gamma exposure dose. The PS/PANI-Cu nanocomposites films were examined as electromagnetic interference shielding material. Electromagnetic shielding effectiveness of the produced nanocomposites were tested in the X-band of the radio frequency range namely from 8 to 12 GHz using the vector network analyzer (VNA) and a proper wave guide. All samples were studied before and after 50 kGy gamma-ray irradiation under the same condition of pressure and temperature. The results showed that the nanocomposites have improved shielding properties.

Abstract Photocatalytic membranes are effective in removing organic dyes, but their low UV resistance poses a challenge. To address this, self-protected photocatalytic PVDF membranes were developed using polyaniline (PANI) and polydopamine (PDA), whaich are anti-oxidation polymers, as interlayers between the membrane and TiO2. PVDF membranes were first modified by a self-polymerization layer of either PANI or PDA and then coated with titanium dioxide (TiO2). The TiO2 remained firmly attached to the PANI and PDA layer, regardless of sonication and prolonged usage. The PANI and PDA layers enhanced the durability of PVDF membrane under UV/TiO2 activation. After 72 h of irradiation, PVDF–PDA–TiO2 and PVDF–PANI–TiO2 membranes exhibited no significant change. This process improved both separation and photocatalytic activity in dye wastewater treatment. The PVDF–PDA–TiO2 and PVDF–PANI–TiO2 membranes showed enhanced membrane hydrophilicity, aiding in the rejection of organic pollutants and reducing fouling. The modified membranes exhibited a significant improvement in the flux recovery rate, attributed to the synergistic effects of high hydrophilicity and photocatalytic activity. Specially, the flux recovery rate increased from 17.7% (original PVDF) to 56.3% and 37.1% for the PVDF–PDA–TiO2 membrane and PVDF–PANI–TiO2 membrane. In dye rejection tests, the PVDF‒PDA‒TiO2 membrane achieved 88% efficiency, while the PVDF‒PANI‒TiO2 reached 95.7%. Additionally, the photodegradation of Reactive Red 239 (RR239) by these membranes further improved dye removal. Despite an 11% reduction in flux, the PVDF–PDA–TiO2 membrane demonstrated greater durability and longevity. The assistance of PANI and PDA in TiO2 coating also improved COD removal (from 33 to 58–68%) and provided self-protection for photocatalytic membranes, indicating that these photocatalytic membranes can contribute to more sustainable wastewater treatment processes.

In this study, mixed-matrix membranes (MMMs) were fabricated using a composite of UiO-66 and polyaniline (PANI) integrated into a polyether-block-amide (PEBAX) matrix. The successful synthesis of the UiO-66 and PANI@UiO-66 composites and their incorporation into the PEBAX matrix were validated through X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infrared (FTIR) Spectroscopy, Brunauer–Emmett–Teller (BET) analysis, and Thermogravimetric Analysis (TGA). Quantitative permeation tests revealed that the CO2 permeability in UiO-66 based MMMs increased by 90 % at 30 % filler loading (from 82 to 156 Barrer), and by 45 % (from 82 to 119 Barrer) in PANI@UiO-66 based MMMs, alongside substantial improvements in selectivity. For UiO-66 membranes we observed a selectivity drop for both gas pairs (CO2/CH4 and CO2/N2) that led to our motivation to modify the MOF. The CO2/CH4 selectivity of the PANI@UiO-66 based MMMs enhanced from 22 to 29 (34%) and the CO2/N2 selectivity from 48 to 57 (18%). Mixed-gas permeation tests further confirmed the efficacy of the membranes in real-world separation scenarios. The diffusivity and solubility results provide insights into the gas transport mechanisms, revealing the synergistic effects of filler incorporation on membrane performance. The integration of UiO-66 and PANI with PEBAX offers a promising pathway for developing efficient and effective gas separation technologies, aligning with the industrial requirements for environmental sustainability and energy efficiency.

The PANI-NiO composites were synthesized by employing an in situ chemical polymerization technique, with varying weight percentages of NiO dopant (PANI-5%NiO and PANI-10%NiO). Additionally, AC conductivity, dielectric constant and dielectric loss were investigated within a frequency range from 20 Hz to 1 MHz. XRD confirmed the phase purity and high crystallinity. SEM reveals the granular shape with a porous surface. In addition, the incorporation of NiO with different concentrations influences the composite’s dielectric properties. All samples exhibited frequency-dependent dielectric properties in line with the Maxwell–Wagner model. Notably, the AC conductivity of PANI-10% NiO composite increased as the frequency increased, this behaviour was certified with Jonscher’s power law. The I–V characteristics confirm the ohmic nature of all synthesized samples. Therefore, the potential of PANI and PANI-NiO composites, as efficient dielectric materials, has been explored and can be useful for device applications in diverse fields.

The redox activities of polyaniline (PANI) are hindered by the instability of pernigraniline salt (PS) state which degrades into oligo‐aniline. In this work, the use of protic additives is examined to mitigate capacity fading and increase utilization of PANI in nonaqueous electrolytes. The protic additive propylene glycol, with its hydrogen‐bonding capabilities, stabilizes the PS PANI and promotes reversible redox reactions, facilitating high capacity and an extended cycle lifetime for applications in metal ion supercapacitors. The use of this protic nonaqueous electrolyte in a PANI–zinc device results in an energy density of 255 Wh kg−1 at a power density of 1.8 kW kg−1 and a robust cycle lifetime of 3,850 charge/discharge cycles. The PANI at a high current density of 6.5 mA cm−2 reaches a capacity of 257 mAh g−1, equivalent to 87% of the its theoretical capacity, showcasing the effectiveness of the protic additive in improving both capacity and cycle life in electrochemical supercapacitors.

Fibrin clots are crucial for hemostasis and the healing of wounds; nevertheless, excessive blood clotting plays an important role in many chronic diseases, including cardiovascular disease. In this study, we demonstrated the effect of the prepared AuNPs@PANI core/shell on the formed fibrin network. The synthesis of nanoparticles combining electrically conducting polymers polyaniline (PANI) and gold nanoparticles (AuNPs) is an appealing field of research currently because of their physical features and prospective applications in biochemistry. AuNPs showed surface plasmonic resonance (SPR) properties in the visible region at 520 nm then, after coating with PANI, there was a dramatic red shift to 610 nm. The morphological conformation was confirmed by characterization at the microscopic (TEM, SEM, EDX). The PANI shell plays a crucial role in this system, first enhances the stability of AuNPs core; also, the surface of the PANI shell has positive charges (zeta potential = +17.8 mV), leading to electrostatic interactions with fibrin clots that have negatively charged surfaces. The synthesized core/shell AuNPs@PANI showed good efficiency for degrading fibrin networks under 1:30 h of irradiation by an external source of laser light, which is a result of AuNPs’ ability to absorb light at 520 nm. The degradation of fibrin was observed using a scanning electron microscope (SEM), which showed a clear change in the shape of the network. The appearance of fibrous endings and gaping indicates the beginning of the degradation and melting of the fibrin network in different sites of the clot. Overall, this method could have a major influence on disease states, for example, deep vein thrombosis, through a localized, catheter-based approach.

Abstract Cancer stands as one of the most impactful illnesses in the modern world, primarily owing to its lethal consequences. The fundamental concern in this context likely stems from delayed diagnoses in patients. Hence, detecting various forms of cancer is imperative. A formidable challenge in cancer research has been the diagnosis and treatment of this disease. Early cancer diagnosis is crucial, as it significantly influences subsequent therapeutic steps. Despite substantial scientific efforts, accurately and swiftly diagnosing cancer remains a formidable challenge. It is well known that the field of cancer diagnosis has effectively included electrochemical approaches. Combining the remarkable selectivity of biosensing components—such as aptamers, antibodies, or nucleic acids—with electrochemical sensor systems has shown positive outcomes. In this study, we adapt a novel electrochemical biosensor for cancer detection. This biosensor, based on a glassy carbon electrode, incorporates a nanocomposite of reduced graphene oxide/Fe3O4/Nafion/polyaniline. We elucidated the modification process using SEM, TEM, FTIR, RAMAN, VSM, and electrochemical methods. To optimize the experimental conditions and monitor the immobilization processes, electrochemical techniques such as CV, EIS, and SWV were employed. The calibration graph has a linear range of 102–106 cells mL−1, with a detection limit of 5 cells mL−1.

Abstract This paper reports on the development of a flexible-wearable potentiometric sensor for real-time monitoring of sodium ion (Na+), potassium ion (K+), and pH in human sweat. Na0.44MnO2, polyaniline, and K2Co[Fe(CN)6] were used as sensing materials for Na+, H+ and K+ monitoring, respectively. The simultaneous potentiometric Na+, K+, and pH sensing were carried out by the developed sensor, which enables signal collection and transmission in real-time to the smartphone via a Wi-Fi access point. Then, the potentiometric responses were evaluated by a designed android application. Na+, K+, and pH sensors illustrated high sensitivity (59.7 ± 0.8 mV/decade for Na+, 57.8 ± 0.9 mV/decade for K+, and 54.7 ± 0.6 mV/pH for pH), excellent stability, and good batch-to-batch reproducibility. The results of on-body experiments demonstrated that the proposed platform is capable of real-time monitoring of the investigated ions.

To investigate the electrocatalytic degradation effect of anthracene in coking wastewater, Ti/PbO2, Ti/PANI/PbO2 and Ti/PANI/PbO2-Ce electrodes were prepared by electrodeposition, and the electrodes were subjected to scanning electron microscopy and X-ray diffraction characterization, electrochemical performance test, hydroxyl radical (·OH) production capacity test and accelerated lifetime test.The results showed that the Ti/PANI/PbO2-Ce electrode modified with polyaniline (PANI) and cerium (Ce) had better surface morphology and higher catalytic activity, and could produce more ·OH with an oxygen precipitation potential of 1.83 V and an accelerated lifetime of 720 min.The Ti/PANI/PbO2-Ce electrode was used for the degradation of anthracene in coking wastewater, and the effects of the main factors on the degradation effect were investigated, and the optimal degradation conditions for anthracene were obtained as voltage 14 V, plate spacing of 1.0 cm, electrolyte concentration of 0.35 mol/L, reaction time of 120 min, pH value of 10.The Ti/PANI/PbO2-Ce electrode showed good electrocatalytic performance.

The properties and activity of TiO2-based nanorods as an antifouling agent and a photocatalyst for the catalytic degradation of methylene blue (MB) have been investigated. A modification of TiO2 with SiO2 was first carried out to enlarge the surface area. In order to enhance the TiO­2 photo response to the visible light region, a further modification of TiO2-SiO2 (TS) composites with polyaniline (PANI) was also conducted. The nanorod TiO2 exhibited an anatase structure based on the diffraction patterns. The TEM images showed that some TiO2 molecules were attached around SiO2 with a random orientation. The TiO2-SiO2-PANI (TS-PANI) exhibited the largest specific surface area (SBET) of about 256.85 m2/g. The profile on the AFM images of the composites showed that the nano-roughness of the coatings was confirmed. The photocatalytic activity was evaluated through the decomposition of MB both on the powder and the coated composites. The photocatalytic activity on the coatings was verified due to further application as anti-fouling coatings involving photocatalytic mechanism. The decomposition of MB using TS-PANI powder and TS-PANI coating composites was 89.5% and 90.2 %, respectively, with the irradiation time on the coatings was 20 min longer. The anti-fouling activity through the photocatalytic mechanism and nano-roughness surface was confirmed by the inhibition of barnacle growth on the teakwood surface immersed for two months in the sea.

In this study, ABS copolymers were blended with doped polyaniline (PAni) and undoped polypyrrole (PPy) at concentrations of up to 2.5 % by weight. This allowed to understand how the mechanical and electrical resistivity properties of the ABS copolymer were affected by small quantities of these polymers. Scanning electron microscopy revealed that even with the smallest amounts of PAni or PPy added, significant morphological changes occur. The contact angle values revealed that there is a different limit in the addition of PAni or PPy to maximize the dispersive component effect. Mechanical analysis of the composites indicated that the addition of 0.625 % and 1.25 % PPy produced the highest values of Toughness, 3.87 MJ m-3 and 3.89 MJ m-3, respectively. The stress at rupture varied from 57 to 61 MPa for ABS-PAni composites and from 25 to 61 MPa for ABS-PPy composites. In addition, the strain at break of ABS-PAni composites ranged from 4 to 7 %, while that of ABS-PPy composites varied from 5 to 12 %. Both ABS-PAni and ABS-PPy composites did not reveal significant changes by Thermogravimetric analysis (TGA). Finally, the electrical conductivity (σ) of the composites increased six and eleven-fold, respectively, upon the addition of 2.5 % of doped PAni or undoped PPy, which were considered significant changes.

Conductive polymers have attracted much attention in various applications, owing to their excellent chemical, thermal, and oxidative stability. However, they have low dielectric constant, which limits their performance in electrochemical devices. To overcome this drawback, blending with other polymers helps improving their electrochemical properties. Herein, we investigate structural and electrochemical properties of poly (vinylidene fluoride) (PVDF)/polyaniline (PANI) blends doped with lithium-based salt. Results showed that the blends exhibit phase separation of PANI and PVDF, which is confirmed by the thermodynamic interaction parameter. We found that the interaction between the two polymers enhanced the ionic conductivity from 4.9 × 10−5 S cm−1 for neat PVDF to 5.3 × 10−4 S cm−1 for composition of 50:50 (PANI50), whereas the ionic conductivity was inversely proportional to the temperature. Moreover, by adding lithium salt to the blend, the thermal stability increased from 376.6 to 478.5 °C for PANI50. The ionic conductivity of the blends depends on the PVDF content, which affects the interaction between the two polymers.

Detecting ovarian cancer at an early stage is crucial for enhancing patient outcomes, underscoring the demand for an efficient and non-invasive detection method. Cancer antigen 125 (CA125) is a vital biomarker in ovarian cancer detection, and there is a pressing demand to develop a quick, sensitive, and simple detection method. Nanobiosensors are increasingly being used by scientists due to their high selectivity and sensitivity, allowing for the swift and precise detection of a wide range of biomarkers. This study aimed to design and fabricate an electrochemical nanobiosensor that could accurately and selectively detect CA125. The nanobiosensor employed graphitic carbon nitrides, molybdenum disulfide, and polyaniline (g-C3N4/MoS2/PANI) to stabilize aptamer strands on a modified glassy carbon electrode. The aptasensor was used to perform electrochemical detection of labeled CA125, utilizing methylene blue and label-free ferrocyanide methods. Ferrocyanide and methylene blue detection limits were determined to be 0.196 U.mL−1 for ferrocyanide and 0.196 U.mL−1 for methylene blue, with a linear detection range of 2–10 U.mL−1 for linear detection. The study results showed that the modified electrode exhibited high selectivity towards CA125 and superior stability compared to other biomolecules. The electrochemical aptasensor also displayed impressive performance when analyzing the serum of patients and healthy people. These findings hold significant promise for future investigation in ovarian cancer diagnosis. This novel electrochemical nanobiosensor may aid in the early detection and management of ovarian cancer, ultimately leading to better patient outcomes.

The presence of chromium [Cr(VI)] and lead [Pb(II)] ions in the water bodies have adverse effects on humans and aquatic life. Graphene oxide-based magnetic nanocomposites synthesized in the presence of chitosan (mGO/CS) or polyaniline (mGO/PA) as potential adsorbents for the removal of Cr(VI) and Pb(II) ions. The FTIR (Fourier transform infrared spectroscopy), EDX (Energy dispersive X-ray), XRD (X-ray diffraction) and SEM (Scanning electron microscopy) were employed to investigate the chemical composition, structural, elemental analysis, crystalline size and morphology of the nanocomposites. The FTIR results confirmed the synthesis of the nanocomposites by detecting peaks of specific functional groups. The average crystallite sizes of the mGO, mGO/CS, and mGO/PA nanocomposites were 17, 25, and 23 (nm), respectively, as determined by the Debye-Scherrer equation from the XRD data. Batch adsorption experiments were conducted for Pb(II) and Cr(VI) removal by varying the variables like pH, concentration of metal ions and contact time. The Box Behnken design (BBD) was used to optimize the adsorption parameters. Under the optimum conditions, mGO/CS and mGO/PA showed maximum removal percentages (%R) of 92.36 and 98.7 for Pb(II), and 85.25 and 93.08 for Cr(VI), respectively. The adsorption capacities were 110.84 and 118.44 mg/g for Pb(II), and 87.74 and 111.7 mg/g for Cr(VI) were obtained for mGO/CS and mGO/PA, respectively. The pseudo-second-order kinetic model and Langmuir isotherm fitted well to the experimental data and explain the adsorption mechanism of the nanocomposite materials for both metal ions.

The constant increase in contamination of agricultural products with mycotoxins makes it urgent to develop new methods for their sorption, isolation, and determination. Molecular imprinting is a promising method for recognizing and isolating target molecules based on specifi c sorption mechanism. The work considers the possibility of obtaining and practical use of mycotoxin–specifi c selective sorbents based on imprinted polyaniline structures using a structural analogue of the mycotoxin zearalenone – 4-hydroxycoumarin. The optimal carrier for the synthesis of molecularly imprinted polymers has been selected. The specifi city of 4-hydroxycoumarin sorption from model solutions has been studied. The practical possibility of sorption and extraction of ZEA from an artifi cially contaminated wheat extract has been demonstrated.

For improving the anti-corrosion performance and durability of waterborne epoxy coatings in high-salt， high-humidity marine environments， polyaniline/boron nitride nanoparticles (PBN) were prepared by the in-situ polymerization of polyaniline (PANI) on the surface of hydroxylated hexagonal boron nitride (BN).In addition， PBN were used as anti-corrosion filler to enhance the anti-corrosion performance of waterborne epoxy coatings.The structure and micro-morphology of nano-particles were characterized by Fourier transform infrared spectroscopy(FT-IR) and scanning electron microscopy (SEM).Moreover， electrochemical tests and neutral salt spray tests (NSS) were used to explore the effects of BN， PANI modifications and PBN addition amount on the anti-corrosion performance of waterborne epoxy coatings.Results showed that PANI grew in situ on the surface of BN nanosheets to form a coral-like structure， and the bonding strength of waterborne epoxy coating reached 6.05 MPa after adding 0.50%(mass fraction，the same below) PBN.The corrosion current density (1.99×10-9 A/cm2) of the composite coating immersed in 3.5%NaCl solution after 120 h was reduced by about 3 orders of magnitude compared to that of pure epoxy coating (1.01×10-6 A/cm2).This was attributed to the fact that the addition of 0.50%PBN could evenly disperse in the epoxy resin， fill small gaps in the coating and enhance the barrier effect against corrosive medium.Meanwhile， PANI had a corrosion inhibition effect， which could synergistically improve the anti-corrosion performance of pure epoxy coatings.

Abstract Early diagnosis of cancer demands sensitive and accurate detection of cancer biomarkers in blood. Carbon dots (CDs) bio-functionalization with antibodies, peptides or aptamers have played significant role in cancer diagnosis and targeted cancer therapy. Herein, a biosensor for detection of cancer biomarker carcinoembryonic antigen (CEA) in blood serum has been designed using CDs bio-functionalized with HRP-conjugated CEA antibody (CUCDs@CEAAb2) as detection probe. CDs were synthesized by upscaling of cow urine, a nitrogen rich biomass waste, by hydrothermal method. Detection probe based on CDs resulted in 3.5 times higher sensitivity as compared to conventional electrochemical sandwich immunoassay. To further improve the sensor performance, hyper-branched polyethylenimine grafted poly amino aniline (PEI-g-PAANI) was used as the sensing interface, which enabled immobilization of higher amount of capture antibody. Detection of CEA in human blood serum coupled with wide linear range (0.5–50 ng/ml), good specificity, stability, reproducibility and low detection limit (10 pg/ml) signified the excellence of CUCDs based CEA immunosensor. CUCDs exhibited excitation wavelength dependent fluorescence property and showed strong blue emission under UV irradiation. MTT assay indicated that the material is not toxic towards human dental pulp stem cells (hDPSCs) and MG63 osteosarcoma cells (cell viability > 90%). The present study demonstrates a methodology for valorization of animal waste to a cost-effective carbon based functional nanomaterial for clinical detection of cancer biomarkers.

The application of solar steam generation in seawater desalination is an effective way to solve the shortage of fresh water resources. At present, many kinds of photothermal conversion materials have been developed and used as evaporators in seawater desalination. However, some evaporators need additional thermal insulation or water supply devices to achieve efficient photothermal conversion. In addition, their complex, time consuming and no scalable preparation process, high cost of raw materials and poor salt resistance hinder the practical application of these evaporator. Owing to its distinctive nanoporous structure, diatomite as fossilized single-cells algae diatoms is a promising natural silica-based material for seawater desalination. They are taken from sea and that makes true sense to use them in the sea. Herein, we report the first example of synthesis robust three-dimensional (3D) natural-diatomite composite by assembling polyaniline nanoparticles covered diatomite into the polyvinyl alcohol pre-treated melamine foam frameworks and demonstrate its application as new evaporator for seawater desalination. The porous framework does not only improve the sunlight scattering efficiency, but also offer large network of channels for water transportation. The inherent mechanism behind salt desalination process involves the absorption of water molecules on the surface of the internal silica micro-nano pores, and evaporation under the heat induced by the polyaniline absorbed sunlight. Meanwhile, the metal ions are segregated by many available pores and channels to achieve the self-desalting effect. The developed evaporator possesses the superiority of multi-stage pore structure, strong hydrophilicity, low thermal conductivity, excellent light absorption, fast water transportation and salt-resistant crystallization as well as good durability. The evaporation rate without an additional device is found to be 1.689 kg m−2 h−1 under 1-Sun irradiation, and the energy conversion efficiency is as high as 95%. This work creates a platform and develops the prospect of employing green and sustainable natural-diatomite composite evaporator for practical applications of seawater desalination.

Significant ethical and health concerns have been brought up recently by the illegitimate use of highly strong synthetic opioids, including fentanyl, as doping agents in sports. Therefore, the requirement for quick and accurate detection techniques to spot illicit drugs in athletes has never been more important. Our study presents a novel biosensor for the sensitive detection of fentanyl based on a nanocomposite of polyaniline (PANI) and a glassy carbon electrode modified with g-C3N4, which is the first of its kind. The g-C3N4-PANI nanocomposite's successful synthesis was confirmed by structural investigations performed using SEM, XRD, and FT-IR. Studies on the electrochemical effects of g-C3N4 and PANI using cyclic voltammetry (CV) and amperometry revealed that the g-C3N4-PANI hybrid composite enhanced the sensitivity, selectivity, stability, and accuracy of fentanyl measurement. With a sensitivity of 0.45445 μA/μM, the electrochemical measurements revealed a broad and consistent linear range spanning from 10 to 920 μM. The detection threshold was established at 0.006 μM. Additionally, its performance was assessed using several real-samples made from athlete pee. The findings displayed satisfactory recovery values ranging from 90.00% to 98.00% and low relative standard deviation values (less than 4.74%) and demonstrated the g-C3N4/PANI nanocomposite-based biosensor has the potential to be an effective anti-doping control tool, opening the door for its practical use in maintaining the fairness and safety of competitive sports. The analysis of the nanocomposite showed that the combination of PANI and g-C3N4 resulted in a material with enhanced electrochemical properties, which contributed to the high performance of the biosensor.

Polyaniline (PANI) was prepared by in-situ polymerization and compounded on the two-dimensional network structural multi-walled carbon nanotube film (CNTF). Compared with the CNT/PANI composites fabricated by using CNT powders or dispersions, the compact and continuous network structure of CNTF/PANI is beneficial to both the thermoelectric and mechanical properties of the composites. The resultant CNTF/PANI composites with PANI polymerization time of 5 h obtain an electrical conductivity of 1 338.4 S/cm and Seebeck coefficient of 63.3 μV/K at 360 K, which are 168.7% and 5.7% higher than those of the CNTF (498.1 S/cm and 59.9 μV/K at 360 K). Consequently, a maximum power factor of 536.8 μW·m−1·K−2 at 360 K is acquired, which is about 2 times higher than that of CNTF (181.7 μW·m−1·K−2 at 360 K). The electrical conductivity of the composites could maintain 93.3% after being bent for 500 times, indicating the excellent flexibility. The tensile strength, Young's Modulus and toughness of CNTF/PANI composites (232.3 MPa, 3.6 GPa and 20.1 MJ/m3, respectively) are 3.5, 2.6 and 2.1 times of those of the CNTF. The flexible, free-standing, lightweight and high-strength CNTF/PANI composites reveal the excellent thermoelectric performance, which are promising in the applications in wearable thermoelectric devices.

Abstract Extensive research is being carried out on the degradation of water pollutants using various strategies to overcome the global water crisis. In the present study, xerogels as a better alternative is utilized to metal oxides for the photocatalytic degradation of toxic water pollutants such as dyes. Xerogels of polyaniline (PANI) and polypyrrole (PPy) are synthesized using phytic acid as a dopant as well as cross‐linker in the weight ratios of 1:1, 1:2, and 2:1 via simple chemical oxidative polymerization. The synthesized xerogels are analyzed for their spectral, morphological, thermal, and optical properties using FTIR, UV–vis, XRD, SEM, and TGA techniques. The xerogels are also tested for their photocatalytic activity against textile dyes – Methylene Blue (MB), Alizarin Red S, (ARS), Rhodamine B (RhB), and Methyl Orange (MO). Among all the composite xerogels, PANI/PPy‐2/1 showed excellent degradation efficiency of 91% for MB dye, 88% for RhB dye, 96% for ARS dye, and 92% for MO dye respectively. The composite PANI/PPy xerogels showed better degradation efficiency than their pristine counterparts. The fragments of the degraded dyes are examined using the LCMS technique and a tentative dye degradation mechanism is proposed.

Efficient and timely detection of cancer biomarkers is pivotal for enhancing treatment outcomes and mitigating patient mortality. This study addresses the pressing need for a swift, accurate, and non-invasive method to identify cancer antigen 125 (CA125), a vital biomarker in ovarian cancer. Leveraging the growing prominence of nano-biosensors for their high selectivity and sensitivity, we present the development and characterization of an innovative electrochemical nano-biosensor. The sensor, featuring aptamer strands immobilized on a glassy carbon electrode modified with graphitic carbon nitrides, molybdenum disulfide, and magnetic nanoparticles (g-C3N4/MoS2/Fe3O4), demonstrates superior sensitivity and accuracy in CA125 detection. Utilizing methylene blue for electrochemical detection of labeled CA125 and ferrocyanide for label-free detection, our aptasensor achieves a low limit of detection (LOD) at 0.202 U.mL−1 and 0.215 U.mL−1, respectively, with a broad detection range from 2 to 10 U.mL−1. The modified electrode exhibits a pronounced affinity for CA125, demonstrating enhanced stability compared to other biomolecules. Crucially, the evaluation of both patient and normal serum samples underscores the aptasensor's remarkable performance. These findings not only establish a robust foundation for future research in ovarian cancer diagnosis but also highlight the potential clinical impact of our electrochemical nano-biosensor in advancing early cancer detection methodologies.

This study investigated the electrochemical detection of Tryptophan (Trp) in pineapple using a glassy carbon electrode (GCE) modified with nanocomposites of green and chemically synthesized copper oxide-polyaniline (PANI/CuOgrn and PANI/CuOchm). Given the properties of PANI/CuOgrn and PANI/CuOchm that have never been applied in the detection of Trp, it indicates that the development of a highly sensitive and selective sensing platform for Trp-is necessary. Such a platform would take advantage of high electric conductivity, larger surface area, and improved catalytic activity of the nanocomposites. PANI/CuOgrn and PANI/CuOchm nanocomposites were formed by doping polyaniline (PANI) with green and chemically synthesized copper oxide (CuO) nanoparticles. Using Debye-Scherrer the particle sizes of PANI/CuOgrn and PANI/CuOchm were found to be 15 nm and 13 nm, respectively. Through cyclic voltammetry (CV) and square wave voltammetry (SWV), the electrochemical behaviour of CuOch, CuOgrn, PANI/CuOchm, and PANI/CuOgrn electrodes was studied, with the focus on comparing the nanocomposites for tryptophan (Trp) catalysis. GCE-PANI/CuOchm showed a higher current response of 3.2 μA than GCE-PANI/CuOgrn. SWV was used to determine Trp, with the linear range of 5.11 μM to 25.85 μM and limit of detection (LOD) values of 3.947 and 2.037 μM for GCE-PANI/CuOchm, and 3.434 and 2.427 μM for GCE-PANI/CuOgrn. The GCE-PANI/CuOchm electrode achieved a recovered percentage of 96 % to 109 %, with an average RSD value of 18.3 (n=3), while the GCE-PANI/CuOchm electrode achieved a percentage recovery of 85 % to 103 % with an RSD value of 12.7 (n=3). The high recovery percentages for both electrodes confirm their dependability in detecting Trp. The high concentration of Trp-in the fruit and the electrode's sensitivity to identifying Trp-in actual sample analysis may account for the high recovery percentage observed.

In this study, Cobalt Oxide (Co₃O₄) cube-doped polyaniline (PANI) composites were successfully synthesized through an in-situ oxidative polymerization process, with the primary objective of effectively eliminating Methyl Orange (MO) from aqueous solutions. The model dye MO was employed to assess the adsorption efficiencies of both PANI homopolymer and Co3O4 cube-doped composites. The results unequivocally reveal that the composites containing Co3O4 cubes exhibit significantly higher adsorption efficiency compared to undoped PANI. The adsorption kinetics adhere to a pseudo-second-order reaction, highlighting the exceptional effectiveness of these composites in MO adsorption. Furthermore, Response Surface Methodology (RSM) was employed to optimize the critical process parameters for MO removal. Utilizing a quadratic model generated by RSM, the study systematically explored the interplay between several key factors, namely initial pH, contact time, concentration, and temperature, and their impact on the removal rate of MO. Through a comprehensive analysis of the RSM model and experimental results, the optimal conditions for MO removal were identified, achieving a maximum adsorption capacity of 109.97 mg g−1 with a Co3O4 loading of 4 wt%. This study underscores the superior adsorption efficiency of Co3O4 cube-doped PANI composites in the removal of MO from aqueous solutions. Additionally, the incorporation of RSM has yielded valuable insights into process optimization, elucidating the intricate relationship between experimental factors and the rate of MO removal. These compelling findings carry profound practical implications, offering a promising avenue for the development of efficient water treatment processes and environmental remediation techniques and possibilities for addressing water pollution challenges.

In order to enhance the physical barrier performance of polyaniline(PANI)/polyurethane(PU) coating against corrosive medium, the introduction of two-dimensional material in the coating is one of the effective methods. PU coating matrix was synthesized from 2, 4-diisocyanate (TDI) and 3, 3′-dichloro-4, 4′-diamino diphenylmethane(MOCA), and MXene@PANI was synthesized by intercalation reaction of PANI with Ti3C2Tx.Then protective coating of MXene@PANI/PU was obtained by adding MXene@PANI into PU. The results show that when the mass ratio of MXene/PANI is 1∶1, no obvious corrosion occurs on the surface of the MXene@PANI/PU coating after 60 days of salt spraying. The corrosion current is 3.709×10-9 A·cm-2, and the impedance modulus is 1.93×108 Ω·cm2. The reason is that MXene improves the electrochemical activity of PANI and thus enhances the electrochemical anticorrosion performance of PANI. On the other hand, MXene nanoplates as a two-dimensional barrier can prevent the corrosive medium from entering into the coating, which improves the long-term protective performance of the coating.

In this study, a manganese dioxide (MnO2/polyaniline (PANI)/ single-walled carbon nanotube (SWCNT) nanocomposite electrode was prepared for pseudo-supercapacitors. To reduce the internal resistance of the electrode, increase the capacitance stability, and reduce the cost of single-walled carbon nanotubes, SWCNT was subjected to two-step acid etching. The purity of SWCNT was improved from ~95% to 99.98%. In addition, SWCNT was functionalized by this process. Thus, a nanocomposite was formed by coating PANI around SWCNT. MnO2/PANI/SWCNT were synthesized using the hydrothermal method. Morphological, chemical and thermal analyses of the synthesized nanocomposite structure were carried out. In addition, X-ray diffraction (XRD) was used to determine the crystal structure. Electrochemical analyses were performed using a three-electrode system in a 1 M KOH electrolyte solution. Cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) measurements were performed. The capacitance of the nanocomposite electrode at 400 cycles was 314 mF/cm2, and the capacitance retention stability was calculated at 73.24%. The results showed that the capacitance stability was high, and the supercapacitor was sensitive to redox reactions.

Thermoelectric materials have been the object of interest in energy demand, given their potential for heat capture and the possibility of conversion into electricity. Among the possible thermoelectric materials, polymeric ones have been investigated because they are durable, non-toxic, and reproducible. This work used polyaniline (PANI), a good conductivity polymer, as a matrix to prepare hybrid nanocomposites. Nanoparticles were incorporated into the PANI matrix via solution with m-cresol. Two types of novel nanoparticles were used: zinc oxide (ZnO) synthesized with morphologies of nanoneedles (n-ZnO) and nanoflowers (f-ZnO). Hybrids of graphene oxide (GO) and ZnO with these morphologies (GO/n–ZnO and GO/f–ZnO) were incorporated into the hybrid PANI nanocomposites. Thermal stability was evaluated by thermogravimetric analysis (TGA). An improvement in thermal stability was observed with increasing GO/ZnO nanoparticles, as well as a higher degradation of the polymer matrix for higher levels of ZnO nanoparticles. The absorption bands of nanoparticles and PANI were observed by Fourier infrared spectroscopy (FT-IR). The corresponding characteristic bands of the functional groups were well evidenced, reflecting the success in synthesizing thermoelectric nanocomposites. Those with hybrid nanoparticles (GO/ZnO) had higher values of electrical conductivity (10.8 and 10.5 S cm−1), while those with only ZnO nanoparticles had higher Seebeck coefficient values (166.4 and 67.4 μV K−1). The only one with the highest thermoelectric force factor was PANI/GO/n-ZnO, with a value of 14.79 μW m−1 K−2, which is 49.3 times greater than the pure polymer and 1.5 times greater than the PANI/n-ZnO nanocomposite.

With the rapid expansion of industrial activities, chromium ions are discharged into the environment and cause water and soil pollution of various extents, which seriously endangers the natural ecological environment and human health. In this study, polyaniline/polyvinyl alcohol/amyloid fibril (PANI/PVA/AFL) composite gel beads (PPA) were prepared from polyaniline and amyloid fibrils with HCl as doping acid and PVA as a cross-linking agent. The results showed that PPA was an irregular composite bead with a diameter of 6 mm. The adsorption of Cr(VI) on the PPA gel beads followed the pseudo-second-order kinetics model, suggesting that chemical reactions were the controlling step in the Cr(VI) adsorption process. Though the Redlich–Peterson isotherm model had the best fit for the adsorption data, the isothermal adsorption process can be simplified using the Langmuir model. The maximum adsorption capacity for Cr(VI) in water was 51.5 mg g−1, comparable to or even higher than some PANI-based nanomaterials. Thermodynamic parameters showed that the adsorption process was a spontaneous, endothermic, and entropy-increasing process. Microscopic analysis revealed that the capture of Cr(VI) on PPA was mainly governed by electrostatic attraction, reduction, and complexation reactions. PPA can be used as a kind of effective remediation agent to remove Cr(VI) in water. HIGHLIGHTS PPA gel beads with bulk sizes were synthesized to remediate Cr(VI) in water.; Adsorption kinetics, isotherms, and thermodynamics of Cr on the PPA gel beads were studied.; PPA showed a high adsorption capacity (51.5 mg g−1) for Cr(VI).; Cr(VI) was almost completely reduced to Cr(III) on the PPA beads.; Electrostatic attraction, reduction, and complexation occurred for the Cr(VI) removal.;

Dyes are the most widely employed materials for coloring applications, especially for industrial purposes; thus, dyes are applied in the textile, cosmetics and foodstuffs. Dyes are very important owing to their applications in all aspects of human life. Accordingly, the production volume of dyes around the world is increasing. In this study, a new type of multifunctional material: polyaniline/Nb2O5/MnO2 and polyaniline/Nb2O5/Cr2O3 nanocomposites, was prepared by chemical polymerization from aniline monomer in the presence of metal oxides (Nb2O5, Cr2O3, and MnO2) and an oxidant (ammonium persulfate) in acidic aqueous solution for the elimination of dye from water. Herein, the nanocomposite was found to be a favorable adsorbent for wastewater treatment due to its high adsorption and efficiency, self-regeneration quality, low cost and easy synthesis. Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy and UV-visible spectroscopy were used to assess the synthesized nanocomposites' characteristics. From the results, we discovered that polyaniline nanocomposites doped with Nb2O5 and MnO2 nanoparticles had a higher adsorption efficiency (~97.37%) than those found in polyaniline with Cr2O3 and MnO2 (~94.3%). We looked at the adsorption conditions, including the medium's pH, the initial dye concentration, the dosage of the adsorbent, and the adsorption time.

Growing volumes of textile waste and heavy metal pollution of water are emerging environmental challenges. In an attempt to tackle these issues, a non-woven sorbent based on jute fibers was fabricated by recycling the textile waste from the carpet industry. The influence of contact time, concentration, pH and temperature on the sorption of lead and copper ions from aqueous solutions was studied. In order to enhance the sorption capacity of the non-woven material, in situ synthesis of polyaniline (PANI) in the presence of TiO2 nanostructures was performed. The contribution of TiO2 nanoparticles and TiO2 nanotubes to the uniformity of PANI coating and overall sorption behavior was compared. Electrokinetic measurements indicated increased swelling of modified fibers. FTIR and Raman spectroscopy revealed the formation of the emeraldine base form of PANI. FESEM confirmed the creation of the uniform nanocomposite coating over jute fibers. The modification with PANI/TiO2 nanocomposite resulted in a more than 3-fold greater sorption capacity of the material for lead ions, and a 2-fold greater absorption capacity for copper ions independently of applied TiO2 nanostructure. The participation of both TiO2 nanostructures in PANI synthesis resulted in excellent cover of jute fibers, but the form of TiO2 had a negligible effect on metal ion uptake.

In this paper, a room-temperature NO2 sensor based on a polyaniline (PANI)/black phosphorus (BP) composite material was proposed to solve the power consumption problem of traditional metal-oxide sensors operating at high temperatures. PANI was synthesized by chemical oxidative polymerization, whereas BP was synthesized by low-pressure mineralization. The PANI/BP composite materials were prepared via ultrasonic exfoliation and mixing. Various characterization techniques, including scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS), confirmed the successful preparation of the PANI/BP composites and their excellent structural properties. The sensor demonstrated outstanding gas sensitivity in the NO2 concentration range of 2–60 ppm. In particular, the sensor showed a response exceeding 2200% at 60 ppm NO2 concentration when using a 1:1 mass ratio of PANI to BP in the composite material.

The development of conducting polymer incorporated with carbon materials-based electrochemical biosensors has been intensively studied due to their excellent electrical, optical, thermal, physical and chemical properties. In this work, a label-free electrochemical dopamine (DA) biosensor based on polyaniline (PANI) and its aminated derivative, i.e., poly(3-aminobenzylamine) (PABA), composited with functionalized multi-walled carbon nanotubes (f-CNTs), was developed to utilize a conducting polymer as a transducing material. The electrospun nanofibers of the composites were fabricated on the surface of fluorine-doped tin oxide (FTO)-coated glass substrate under the optimized condition. The PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers were characterized by attenuated total reflectance–Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), which confirmed the existence of f-CNTs in the composites. The electroactivity of the electrospun nanofibers was investigated in phosphate buffer saline solution using cyclic voltammetry (CV) before being employed for label-free electrochemical detection of DA using differential pulse voltammetry (DPV). The sensing performances including sensitivity, selectivity, stability, repeatability and reproducibility of the fabricated electrospun nanofiber films were also electrochemically evaluated. The electrochemical DA biosensor based on PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers exhibited a sensitivity of 6.88 µA·cm−2·µM−1 and 7.27 µA·cm−2·µM−1 in the linear range of 50–500 nM (R2 = 0.98) with a limit of detection (LOD) of 0.0974 µM and 0.1554 µM, respectively. The obtained DA biosensor showed great stability, repeatability and reproducibility with precious selectivity under the common interferences, i.e., glucose, ascorbic acid and uric acid. Moreover, the developed electrochemical DA biosensor also showed the good reliability under detection of DA in artificial urine.

Aqueous zinc-ion batteries (ZIBs) have attracted burgeoning attention and emerged as prospective alternatives for scalable energy storage applications due to their unique merits such as high volumetric capacity, low cost, environmentally friendly, and reliable safety. Nevertheless, current ZIBs still suffer from some thorny issues, including low intrinsic electron conductivity, poor reversibility, zinc anode dendrites, and side reactions. Herein, conductive polyaniline (PANI) is intercalated as a pillar into the hydrated V2O5 (PAVO) to stabilize the structure of the cathode material. Meanwhile, graphene oxide (GO) was modified onto the glass fiber (GF) membrane through simple electrospinning and laser reduction methods to inhibit dendrite growth. As a result, the prepared cells present excellent electrochemical performance with enhanced specific capacity (362 mAh g−1 at 0.1 A g−1), significant rate capability (280 mAh g−1 at 10 A g−1), and admirable cycling stability (74% capacity retention after 4800 cycles at 5 A g−1). These findings provide key insights into the development of high-performance zinc-ion batteries.

Polyaniline nanofibers (PAni-NFs) have been synthesized under various concentrations (0.12, 0.16, and 0.2 g/l) of aniline and different times (2h and 3 h) by hydrothermal method at 90°C. Was conducted with the use of X-ray diffraction (XRD), Fourier Transform Infrared spectra (FTIR), Ultraviolet-Visible (UV-VIS) absorption spectra, Thermogravimetric Analysis (TGA), and Field Emission-Scanning Electron Microscopy (FE-SEM). The X-ray diffraction patterns revealed the amorphous nature of all the produced samples. FE-SEM demonstrated that Polyaniline has a nanofiber-like structure. The observed typical peaks of PAni were (1580, 1300-1240, and 821 cm-1), analyzed by the chemical bonding of the formed PAni through FTIR spectroscopy. Also, tests indicated the promotion of the thermal stability of polyaniline nano-composite at temperatures above 600°C. Still, the PAni-0.12 g/l sample was better than the other samples, and the optical parameters manifested a decrease in the band gap (Eg) band gap. The observed TGA test findings also promoted Polyaniline's thermal stability at temperatures reaching 600°C.

Nowadays, electromagnetic pollution caused by electronic devices is gradually becoming a concern. Moreover, as the frequency of electromagnetic pollution from electronic devices is mainly in the range of 2–10 GHz, the design of microwave-absorbing materials for this frequency range has become a hot issue. To tackle the issue, core-shell structured hexagonal boron nitride (h-BN) @polyaniline (PAn) composites have been proposed to construct heterogeneous microwave-absorbing materials. Firstly, the h-BN is exfoliated, and hydroxyl functionalized to produce hydroxy boron nitride (OH-BN), which enhances its polarization ability by structuring defects and adding functional groups to improve its microwave absorption efficiency. Afterward, PAn was grafted on the OH-BN surface by in situ polymerization. The microwave absorption properties of OH-BN@PAn composites can be tuned by modulating the doping of PAn. As expected, the OH-BN@PAn composite exhibits superior microwave absorption properties with the minimum reflection loss (RLmin) value of −38.60 dB at 3.5 mm and an effective absorption bandwidth (EAB) of 3.4 GHz (6.24–8.64 GHz) at pH = 2. Also, the composite achieves effective microwave absorption at 3.76–18 GHz by adjusting the matching thickness. Notably, the RLmin value of OH-BN@PAn was successfully tuned from the high-frequency region (12.4 GHz, pH = 0) to the low-frequency region (7.28 GHz, pH = 2) by adjusting the doping degree. In addition, the RL value and EAB width have been increased due to the increased impedance matching and polarization capability. This work can provide a reference for constructing composite microwave-absorbing materials and regulating microwave absorption performance.

Biofouling is a major issue in aquaculture cages and nano materials based antifouling strategies became more prominent in recent years. Polyethylene aquaculture cage net surface which is modified with polyaniline and nano-copper oxide (CuO), reported to have biofouling resistance. Leaching of nano CuO from the net to the aquatic environment and its bioaccumulation in fish is the major concern against the technology adoption. The present study aimed to understand the accumulation of copper in fishes grown in a nano CuO treated aquaculture cage net. Studied the leaching pattern of nano CuO, biofouling inhibition and changes in strength of the cage net due to the nano CuO treatments. Fishes grown in the treated cages exhibited normal growth characteristics with no signs of abnormalities and also copper in their organs were within the prescribed standard limit. The CuO treated cage net exhibited excellent biofouling resistance and the percentage of occlusion of mesh by foulers were 56.77% more efficient than untreated cage net. Rate of nano CuO leached to the aquatic system was less than 8 μg/g·d. The fouling organism assemblage on untreated and treated net was 18 and 11 species, respectively. Major calcareous shelled foulers were absent on treated nets. The study highlighted the potential application of nano CuO treatment to control biofouling in aquaculture cages.

Polyaniline (PANI)-Fe2O3/CuO and PANI -Fe2O3/ZnO hybrid materials were developed and prepared by in situ polymerization at 0°C using ammonium persulfate as oxidant. The resulting products are investigated for their structural properties by X-ray diffraction (XRD), Fourier transform infrared (FTIR), and scanning electron microscopy (SEM), and the results confirm the formation of the hybrid architecture. In addition, the electrochemical properties of the hybrid products are investigated by cyclic voltammetry (CV) and optical properties were determined using UV-Vis Diffuse Reflectance Spectrophotometer (UV-Vis DRS). Compared to PANI/ZnO or CuO, Fe2O3/CuO or ZnO exhibit significantly improved properties. Based on the obtained results, the products thus open the way for a variety of electrical and sensors applications.

The Hall method was used to study the electrical characteristics of composite materials based on polyaniline (PANI), graphene oxide (GO), and manganese. A comparison of these characteristics of GO-PANI and GO-PANI-Mn composite systems with GO and PANI monomaterials was carried out. It was demonstrated that the electrical conductivity of composites was significantly higher than that of monomaterials and was determined by the charge carrier mobility. Based on UV-visible and IR spectroscopy data, it was shown that the optical band gap (Eg) of the GO-PANI composite increased with the addition of metal, but decreased compared to PANI; the shift of characteristic vibrations to lower frequencies indicated a covalent interaction of the GO-PANI composite with manganese cations

Recently, with the development of non-invasive human health monitoring technology including wearable devices, a flexible sensor that monitors ‘human sound and movement signals’ such as human voice and muscle movement is attracting attention. In this experiment, electrospun nanofibers were mixed with highly conductive nanoparticles and coated with polyaniline to detect the patient's electrical signals. Due to the high piezoelectric effect, nanofiber-based sensors do not require charging through a separate battery, so they can be used as self-powered devices. In addition, the LCR meter test confirmed that the sensor has a high capacitance due to its high conductivity and high sensitivity to electrical signals. The sensor produced in this study can visually estimate the electrical signal of the actual human body through real-time comparison with electromyography (EMG) measuring equipment, and it was confirmed that the error is small. This sensor is expected to be widely used in the medical field, from simple sound and movement signals to disease monitoring.

Excellent electromagnetic wave absorption ability and effective absorption bandwidth have been the development direction of electromagnetic wave absorbing materials. In this paper, a rational structural design is proposed. Graphene oxide (GO)/polyaniline (PANI) layer was formed on the surface of the natural material bamboo powder (BP) by an interfacial polymerization process. The combination of GO and PANI improves the impedance mismatch of the conductive polymer PANI. Enhanced dielectric storage and loss capability of the composite GO/PANI/BP. The addition of BP brings more electromagnetic wave loss channels to the composite GO/PANI/BP. This unique structure facilitates the construction of a three-dimensional electromagnetic wave-reflecting cavity, which improves the absorptive capacity of the composite by introducing effective multiple reflections. The conductivity of GO/PANI/BP was 1.78 (±0.06) S/cm. When filled to 30 wt%, a minimum reflection loss (RLmin) of −44 dB at 9.36 GHz and a thickness of 3 mm, and an effective absorption bandwidth (

The electrodeposition of polyaniline films is usually carried out in acid solutions such as hydrochloric acid, perchloric acid or sulfuric acid, and more rarely in organic acids such as camphorsulfonic acid (CSA). In this study, the impact of the presence of a surfactant in the electrolytic solution based on hydrochloric acid or CSA was evaluated by successively using anionic (sodium dodecyl sulfate, SDS), cationic (cetyltrimethylammonium bromide, CTAB), and non-ionic (Tritonx100) surfactants. Whatever the surfactant and the acid used, the electrochemical oxidation of aniline has successfully led to the formation of a thick polyaniline (PANI) film through a quasi-reversible reaction controlled by the diffusion of aniline monomers. The nature of the surfactant was shown to affect physico-chemical properties of the film, in particular its morphological features (morphology, thickness, roughness), electrochemical activity, specific capacitance, and conductivity. For example, PANI films containing SDS had a spongy morphology when PANI films containing Tritonx100 had a more fibrous and compact structure. Glow Discharge Optical Emission Spectroscopy (GDOES) experiments also highlighted differences depending on the acid used since chloride anions, from HCl, were present only on the top surface of the PANI films when camphorsulfonate anions were present everywhere throughout the polymer film, which impacts the doping process and electrochemical activity of the films. Moreover, the specific capacitance of the PANI/CSA films is higher and more sensitive to current density variation than the one of PANI/HCl films. Finally, electrochemical impedance experiments evidenced that the conductivity of PANI films electrodeposited from CSA solutions was much higher than the one of PANI films prepared from HCl solutions, and highly dependent on the nature of the surfactant, the most conductive films being obtained in the presence of SDS and Tritonx100. Therefore, the originality of this work comes from the possibility of modulating the conductivity, capacitance and electroactivity of electrodeposited polyaniline films using surfactants of different polarity, and from the determination of the distribution of ions in the films using the GDOES technique, which is rarely used to characterise organic films.

Gold nanoparticles (Au NPs) with graphene oxide (GO) shell (Au@GO), silver nanoparticles (Ag NPs) with GO shell (Ag@GO), and gold silver nanoparticles (AuAgNPs) with GO shell (AuAg@GO) were synthesized employing a cationic surfactant. The prepared core@shell structures were used for in situ synthesis of long tubular polyaniline structures employing cetyl trimethyl ammonium bromide (CTAB) as a soft template. This process led to a notable enhancement in the tubular nanostructure of PANI, extending its length beyond 10 μm, in the case of using core/shell Au@GO, Ag@GO, and AuAg@GO structures. To evaluate their applicability and compatibility, the dispersibility of these nanocomposites was assessed in three distinct solvents: water, dimethyl sulfoxide (DMSO), and N-Methyl-2-pyrrolidone (NMP). Subsequently, the dedoping of PANI within the prepared nanocomposites was scrutinized using UV–Visible (UV–Vis) spectroscopy, which revealed a reduction in the I750/I315 ratio from 1.00 to 0.66 when subjected to water and NMP solvents, respectively. Notably, the dedoping of the AuAg@GO/PANI nanocomposite was predominantly observed in NMP, attributable to the presence of hydrogen bonding interactions and the basic properties of NMP. In terms of ionic conductivity, it was observed that the prepared nanocomposite exhibited its highest conductivity in a water-based medium, registering at 1982 μs. Furthermore, the AuAg@GO/PANI nanocomposite exhibited superior sensing capabilities in comparison to PANI-based gas sensor devices, particularly when exposed to acetone, CO2, NO2, and H2S. Remarkably, at room temperature (25 °C), the AuAg@GO/PANI nanocomposite displayed rapid response and recovery times, with values of 279 s, 431 s, 335 s, and 509 s for 1 ppm concentrations of CO2, NO2, H2S, and acetone, respectively. The sensitivity of these sensors towards acetone, CO2, NO2, and H2S, was quantified by analyzing the slope of the response versus the target gas concentration, revealing the AuAg@GO/PANI nanocomposite to exhibit the highest sensitivity, particularly towards NO2.

Recent research works are based on ternary polyaniline composite with nickel oxides, nickel ferrite, cobalt (II), copper (II) doped with graphene, manganese, PVA, carbon and more. Nickel itself being a magnetic material it is much suitable for super capacitive behaviour. Incorporating Nickel (II) chloride and Benzalazine in polyaniline composite will enhance its electromagnetic, electrochemical and mechanical properties. In the present work, ternary composites containing polyaniline, benzalazine and nickel (II) chloride were synthesized by the oxidative polymerization of aniline with different weight percentages of benzalazine and Nickel (II) chloride. Benzalazine gets physically adsorbed on the polymer chain and nickel ions get coordinated in the polymer chain. X-ray diffraction pattern was carried out to determine the crystalline nature of the synthesized samples. The synthesized polymer composites were subjected to the technique of Ultraviolet visible and Fourier transform infrared spectroscopic techniques to find out the optical properties. Surface morphology of the synthesized samples were analyzed using atomic force microscopy and Scanning electron microscopy. Redox behavior and capacitance studies were carried out by using cyclic voltammetry at different solution pH value and the synthesized composites at solution pH value pH 1.0 found to exhibit well defined capacitance behavior.

Fullerene, an intimate zero dimensional nanocarbon, has been frequently adopted as nanocomposite reinforcement. Imperative utilizations of fullerene and derived nanocomposites have been observed in energy, optical, and electronics devices sectors. Conjugated or conductive polymers have π-conjugation backbone system leading to semiconducting features. In addition to fine electron conduction, these polymers have advantages of low weight, facile processing, and chemical and thermal robustness. Including nanocarbon dopants in conjugated polymers have enhanced several technical features of these matrices. Accordingly, this progressive overview highlights design, properties, and potential of fullerene reinforced conducting polymer nanocomposites. The structural multiplicity of conducting polymer/fullerene nanocomposites enabled advanced features and potential. Consequently, ensuing nanocomposites revealed efficient structural, morphological, and physical characteristics, along with several revolts in technological fields like photovoltaics, supercapacitors, sensors, etc. Forthcoming research on ground-breaking fullerene may daze design/performance challenges towards large scale practical applications.