Electrocatalysis and detection of nitrite on a polyaniline‐Cu nanocomposite‐modified glassy carbon electrode

A polyaniline (PANI)‐Cu nanocomposite‐modified electrode was fabricated by the electrochemical polymerization of aniline and the electrodeposition of copper under constant potentials on a glassy carbon electrode (GCE), respectively. Scanning electron microscope result shows that the PANI‐Cu composite on the surface of the GCE displays the nanofibers having an average diameter of about 80 nm with lengths varying from 1.1 to 1.2 μm. The electrode exhibits enhanced electrocatalytic behavior to the reduction of nitrite compared to the PANI‐modified GCE. The effects of applied potential, pH value of the detection solution, electropolymerization charge, temperature, and nitrite concentration on the current response of the composite‐modified GCE were investigated and discussed. Under optimal conditions, the PANI‐Cu composite‐modified GCE can be used to determine nitrite concentration in a wide linear range (n = 18) of 0.049 and 70.0 μM and a limit of detection of 0.025 μM. The sensitivity of the electrode was 0.312 μA μM^?1 cm^?2. The PANI‐Cu composite‐modified GCE had the good storage stability. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Arsenic detection by nanogold/conducting‐polymer‐modified glassy carbon electrodes

This article discusses the results for the development of a nanogold‐particle/polyaniline‐modified glassy carbon electrode for the detection of arsenic(III) in water. A thin polyaniline film was electropolymerized onto a glassy carbon electrode. The gold nanoparticle was then deposited onto the polyaniline‐coated glassy carbon electrode via potential step electrolysis from 1.1 to 0 V versus Ag/AgCl/NaCl (saturated) for 45 s from a 0.5M H₂SO₄ solution containing 0.1 mM NaAuCl₄ in the absence and presence of a 0.1 mM KI additive. The surface of the modified electrode was examined with scanning electron microscopy. Cyclic and anodic stripping voltammetry of arsenic(III) was performed on the modified electrode. The thus modified nanogold‐particle/polyaniline‐modified glassy carbon electrode prepared in the presence of the I^? (KI) additive showed a high sensitivity in detecting arsenic(III) in water, and with stripping voltammetry, a limit of detection of 0.4 ppb arsenic was obtained, which is much lower than the arsenic guideline limit of the World Health Organization. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1306–1311, 2007     

Investigation of the behavior of hydrogen‐bonded phenolic compounds and their determination by using poly(vinylferrocenium)–polyaniline composite film

The hydrogen bonding between phenolic compounds (phenol (Ph), catechol (Ct), resorcinol (Rs), and hydroquinone (Hq)) is investigated at pH 4. The oxidation behaviors of total phenolic compounds (TotPh) are different from their individual behaviors due to the existence of intermolecular hydrogen‐bonded oligomeric clusters. Theoretical calculations and voltammetric and spectroscopic evidences support the intermolecular hydrogen bonding. The interaction of the phenolic compounds with polyaniline (PANI) and poly(vinylferrocenium) (PVF⁺) films are also investigated electrochemically and spectroscopically. The phenolic molecules are immobilized in both polymers due to the construction of hydrogen bonds by PANI and the complexation with PVF⁺. In addition, Ct and Hq are catalytically oxidized by PANI. Determinations of Ct and TotPh are performed on PVF⁺–PANI composite ‐ coated Pt electrode using amperometric I–t method. Composite coating exhibits significant electrochemical activity toward Ct and TotPh, with high sensitivity and a wide linearity range. The steady‐state currents versus concentration of Ct and TotPh are found to be linear in the range of 1.35 × 10^?3?50.0 mM and 4.10 × 10^?4?560 mM for two linear regions, respectively. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43596.     

High‐sensitivity QCM with multielectrode piezoelectric quartz crystal design

The ideal linear elastic, small hysteresis phenomenon makes the quartz resonator uniquely useful for Quartz Crystal Microbalances (QCM). Enhanced high‐precision integrated quartz crystal resonators were designed based on the common‐mode rejection principle. The internal stress of quartz crystal on the force was analyzed for the multielectrode design, and the point which located the electrode (diameter is 1 mm) is distributed on the circle from 4 mm to the center of the quartz crystal plate, and the orientation angle φ=60°. The 15 group difference frequency signals were first done the difference frequency processing and then superposition by information fusion technology. The final force sensitivity coefficient of integrated resonator is 11223 Hz/N. It is 10 times than the single resonator. The frequency stability of each electrode is shown 10^?10 order of magnitudes.     

Gold nanoparticle patterned on PANI nanowire modified transducer for the simultaneous determination of neurotransmitters in presence of ascorbic acid and uric acid

In the present work, we have electrochemically deposited polyaniline nanowires (PANIS) on glassy carbon electrode (GCE) from its monomer liquid crystalline template of anilinium‐3‐pentadecyl phenyl sulphonic acid (An⁺ PDPSA^?). Further, electrode was modified by the electrochemical patterning of gold nanoparticles on the PANIS/GCE (PANIS/Au/GCE) by electrodeposition through chronoamperometry. Modified electrode characterized by electrochemical impedance, morphology, XRD, electroactive surface area, and later demonstrated its efficacy for the individual and simultaneous sensing of dopamine, ascorbic acid, serotonin, and uric acid. Finally, its performance in the real sample (blood serum) was evaluated. The superior electrocatalytic performance with higher sensitivity suggested that the modified electrode can be used as an excellent transducer for the sensing of neurotransmitters. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133 , 44351.     

Impedimetric detection of dopamine on poly(3-aminophenylboronic acid) modified skeleton nickel electrodes

Detection of biologic compounds in particular dopamine is usually based on the complexation between boronic acid groups and diols. For this reason the development of new sensors based on direct monitoring of boronic acid–diol complexation is attractive. A measurable electric response due to a change in the dopamine concentration can be achieved on electrodes modified with boronic groups. In this work a modified electrode has been obtained by electropolymerization of 3-aminophenylboronic acid in aqueous solutions on a preformed polyaniline layer electrochemically deposited on smooth and skeleton nickel electrodes. The modified electrodes have been tested as impedimetric sensors for the detection of dopamine in aqueous phosphate buffer at pH = 7.4. Both sensors gave a linear response for dopamine concentrations between 10^?5 and 10^?10 mol L^?1. Poly(3-aminophenylboronic acid) modified skeleton nickel electrode has the advantage of an increased specific surface area, that lead to a high density of boronic acid groups and hence to a better sensitivity.     

Thorium (IV) phosphate‐polyaniline composite‐based hydrophilic membranes for bending actuator application

In the present study, ionic polymer metal composite (IPMC) membrane actuator based on triple‐layered thorium(IV) phosphate/polyaniline/Pt (ThP‐PANI‐Pt) was prepared via consecutive solution recasting and electroless plating methods. The triple‐layered membrane is composed of thorium(IV) phosphate (ThP) inorganic cation exchanger layer in the middle section, two layers of polyaniline deposited through in situ polymerization and finally Pt electrode layers on both the surfaces on the outer section. The water uptake capacity of the ThP‐PANI composite polymer membrane was found to be 95.40% at 45ºC for 10 h of immersion time. The ion exchange capacity and proton conductivity was found to be 1.6 meq g^?1of dry membrane and 1.12 × 10^?3 S cm^?1, respectively. Maximum water loss from IPMC was 38% at 4 V for a time period of 12 min. Scanning electron micrographs shows the smooth and uniform coating of Pt on both side of composite polymer membrane surfaces. Cyclic voltammetry, linear sweep voltammetry, transmission electron microscopy, Fourier transforms infrared spectroscopy, thermal gravimetric analysis, X‐ray diffraction, and tip displacement of ThP‐PANI‐Pt IPMC membrane actuator was also examined. POLYM. ENG. SCI., 57:258–267, 2017. © 2016 Society of Plastics Engineers     

New conductive thermoplastic elastomers. Part II. Physical and chemical‐physical characterization

To overcome the problems relevant to the low processbility and scarce mechanical properties of polyaniline, in a previous work we have proposed the synthesis of elastomeric conducting copolymers prepared by grafting polyaniline (EB) or sulfonated polyaniline (SPAN) chains to the backbone of a carboxylated segmented polyurethane (PEUA). In the present work the physical and chemical‐physical properties of the copolymers are investigated. As evidenced by thermal (DSC) and dynamo‐mechanical (DMTA) characterization, the introduction of EB or SPAN in the matrix enhances the hard‐soft phase segregation effect, because of the strong tendency of the conductive polymer chains to aggregate. Moreover, the EB and SPAN chains, grafted to the polyurethane backbone, acting as reinforcing filler, give rise, compared with the mechanical properties of the insulating matrix, to an increase of the Young modulus and a decrease of the tensile set. When the copolymers are HCl doped their electrical conductivity increases many orders of magnitude, reaching values of about 10^?3 Ω^?1 cm^?1. The conductivity, measured along the deformation direction, may be further increased by stretching the copolymer films. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1259–1264, 2002     

m‐Chloroaniline emulsion polymerization,macromolecular chain structure and electrochemical properties

Poly(m‐chloroaniline) (PmClAn) was synthesized by emulsion polymerization. The influences of reaction temperature and initiator concentration on polymerizations were studied. It was found that PmClAn with number‐average molecular weight of 1.85 × 10³ g mol^?1 was obtained by the following conditions: 80 °C, [monomer] = 0.187 × 10^?3 mol l^?1, [sodium lauryl sulfate] = 4.8 × 10^?2 mol l^?1, [potassium peroxydisulfate] = 5.6 × 10^?2 mol l^?1, reaction period = 2.0 h. ¹H NMR, FTIR, and transmission and scanning microscopy were used for structural characterization of PmClAn. It was shown that the ratio of benzoid to quinoid units in the macromolecular chain was respectively 3:2, and that PmClAn has a typical crystalline monoclinic form. A PmClAn molecular chain configuration was also proposed on the basis of crystallographic data. Cyclic voltammetry experiments revealed the PmClAn membrane electrode electroactivity. This electroactivity increased when the polymer was proton‐doped. When Pt particles were electrodeposited onto the polymer membrane electrode, they presented a preferred orientation. Isopropanol oxidation intensities with platinized PmClAn modified electrodes were larger than with a platinized Pt electrode. We also found that oxidation occurred mainly on the Pt particles deposited on the polymer, and that the anodic peak potential changed with polymer and its doping level. These results indicated that the Pt particles interacted with the polymer and that catalytic properties could be observed. © 2002 Society of Chemical Industry     

Electroreduction of hexavalent chromium by polyaniline

BACKGROUND: A plate‐gap model interpretation of enzymatic reaction kinetics and rotating disc voltammetry were applied for evaluation of the nature of the reaction of the electroreduction of Cr(VI) (as dichromate ions) on a polyaniline (PANI)‐modified glassy carbon (GC) electrode. RESULTS: The kinetic parameters (the maximal current (V_max) and Michaelis constant (K_M)) for electroreduction of Cr(VI) on the PANI‐modified GC electrode were determined as V_max = 0.34 × 10^?7 mol cm^?3 s^?1 and K_M = 0.47 × 10^?6 mol cm^?3. The reduction of dichromate is intensified by PANI film growth. CONCLUSION: To characterise the electroreduction of Cr(VI) on a PANI‐modified GC electrode, the kinetic parameters of the reaction were determined using a plate–gap model interpretation of enzymatic reaction kinetics and rotating disc voltammetry. The catalytic nature of Cr(VI) electroreduction on the PANI‐modified electrode has been shown. Copyright © 2009 Society of Chemical Industry     

Preparation of poly(9‐aminoacridine)‐modified electrode and its application in the determination of dopamine and ascorbic acid simultaneously

A novel modified electrode was fabricated with 9‐aminoacridine by electropolymerization in the phosphate buffer solution (PBS) (pH 7.4) and was characterized by cyclic voltammetry (CV). The modified electrode showed excellent electrocatalytic effect and high stability toward the electrochemical oxidation of dopamine (DA) and ascorbic acid (AA). Also, it showed a high stability for the determination of DA and AA simultaneously. Well‐separated voltammetric peaks were observed for DA and AA on the modified electrode. The separation of two anodic peaks was 170 mV, which was large enough to eliminate the interference of AA and determine DA. The differential pulse voltammograms (DPV) were used for the measurement of DA by means of the poly(9‐aminoacridine)‐modified electrode in PBS at pH 7.4. A linear response toDA was observed in the concentration range from 1.5 × 10^?6 to 3.5 × 10^?3 mol L^?1 with a correlation coefficient of 0.9998 and a detection limit (S/N = 3) of 1.0 × 10^?7mol L^?1. The proposed method was used to determine DA in DA‐hydrochloride injection and showed excellent sensitivity and recovery. The ease of fabrication, good reproducibility, high stability, and low cost of the modified electrode are the promising features of the proposed sensor. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3864–3870, 2007     

Strong effects of counterions on the electrochemistry of poly(N‐methylaniline) thin films

Poly(N‐methylaniline) thin films show different cyclic voltammetric behaviour when cycled in HClO₄, HBF₄, HCl or HNO₃. While in the first two acids the film shows profiles peak potentials similar to those of polyaniline, profiles in HCl and HNO₃ show higher peak potentials for oxidation and a different shape. The free energy for the process, calculated from the oxidation peak potential, shows a linear correlation with the free energy of hydration of the anions present in the test solution. An energy cycle for the oxidation process is proposed to explain the results. The reaction mechanism assumes that anions have to lose their hydration shell to form the polymer salt during electrochemical oxidation of the films. Electropolymerization also depends on the anion present in the solution. While this is possible with low hydration energy anions (ClO₄^?, BF₄^?), it is difficult or impossible when the electrolyte solution contains other anions (Cl^?, NO₃^?) where a higher oxidation potential of the preformed polymer is observed. © 2002 Society of Chemical Industry     

Electrochemistry of polyaniline: Study of the pH effect and electrochromism

Polyaniline was electrochemically synthesized from an aqueous medium with various acid electrolytes via potentiodynamic and potentiostatic techniques. The electrochemical synthesis of polyaniline was studied over various substrates, including Pt, Ti, Ni, and SnO₂ coated glass, and in various acid electrolytes. Cyclic voltammograms of electrochemically synthesized polyaniline were studied in HCl in a pH range of 1–4. Probable electrochemistry and chemical changes were deduced that occurred when polyaniline film was electrochemically oxidized and reduced between ?0.2 and 1.0 V versus a Ag/AgCl reference electrode in an acidic electrolyte at pH 1, and three corresponding oxidation and reduction peaks were described instead of two redox peaks (as observed by W. S. Huang, B. D. Humphrey, and A. G. MacDiarmid, J Chem Soc Faraday Trans 1 1986, 82, 2385). The electrochromic property was studied with changes in the chemical states of polyaniline during electrochemical oxidation and reduction. A new viscous electrolyte, aqueous AlCl₃ (pH 2), saturated with AgCl was used for the construction of an electrochromic display device. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 378–385, 2002     

Design,synthesis and characterization of a novel self‐doped polyaniline derivative

A type of self‐doped polyaniline derivative was successfully synthesized using an oxidative coupling polymerization approach. The structure of the electroactive polymer was investigated using Fourier transform infrared and ¹H NMR spectroscopy and gel permeation chromatography. Its thermal and spectral properties were characterized using thermogravimetric analysis and UV‐visible spectroscopy. The electrochemical activity of the polymer was studied using cyclic voltammetry (CV) in 1.0 mol L^?1 H₂SO₄ solution with various scan rates. The peak current increases linearly with scan rate from 10 to 120 mV s^?1, which indicates that the electrode reaction is controlled by a surface process. In addition, the self‐doped characteristic was investigated using CV in 1.0 mol L^?1 KCl solution with pH value changing from 1 to 12, and the results indicate that the polymer has excellent electrochemical activity even in neutral and alkaline environments. Copyright © 2010 Society of Chemical Industry     

A highly oriented poly(3,4‐ethylenedioxythiophene) film: Facile synthesis and application for supercapacitor

A single crystal poly(3,4‐ethylenedioxythiophene) (PEDOT) film with highly oriented arrangement has been fabricated from an aqueous solution by a novel unipolar pulse electropolymerization method. Film formation mechanism was proposed based on the in situ mass change during electropolymerization process measured by the electrochemical quartz crystal microbalance. The compositions, morphology and crystal structure of the fabricated films are characterized by Fourier transfer infrared spectroscopy, scanning electron microscopy, and X‐ray diffraction, respectively. It is found that the prepared PEDOT film on carbon nanotubes (CNTs)‐modified electrode with a spongy dendritic structure possesses outstanding electroactivity, high specific capacitances (239.1 F?g^?1, including the specific capacitances of CNTs which is 21.4 F?g^?1), and excellent cycling stability with 7.3% decay from its initial capacitance over 10,000 cycles. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43418.     

Zinc ion-imprinted polymer based on silica particles modified carbon paste electrodes for highly selective electrochemical determination of zinc ions

ABSTRACT

In this study, Zn(II) ion-imprinted polymer was prepared on the surface of vinyl silica particles and applied for detection of Zn(II) ions using differential pulse voltametry. The ion- imprinted polymer particles were prepared by free radical polymerization. The prepared particles were characterized by different morphological and elemental techniques. The ion-imprinted particles were used to fabricate the carbon paste electrode as a zinc ions sensor. The modified zinc sensor showed linear response in the concentration range 6.12 × 10^?9 to 4.59 × 10^?8 mol L^?1. The limit of detection and limit of quantification of the electrode were 1.351 × 10^?8 and 4.094 × 10^?8 mol L^?1, respectively.     

Electrochemical supercapacitor properties of polyaniline thin films in organic salt added electrolytes

We demonstrate optimized supercapacitive characteristics of electrodeposited polyaniline by adding organic salt into electrolyte. The optimum amount of the organic salt is found to be 2 wt % which provides better ionic conductivity of the electrolyte, leading to the improved specific capacitance of 259 Fg^?1. This capacitance remains at up to 208 Fg^?1 (80% capacity retention) after 1000 charge–discharge cycles. The optimized organic salt added electrolyte causes better rate performance and higher cyclability. Significantly reduced electrochemical charge transfer resistance at the electrode/electrolyte interface results in the increased ionic conductivity, which can be useful in electrochemically preferred power devices for better applicability. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40306.     

A novel polymer‐based genosensor for the detection and quantification of Streptococcus pneumoniae in genomic DNA sample

The Streptococcus pneumoniae detection plays an important role in the diagnosis and monitoring of pneumococcal diseases. A genosensor based on graphite electrodes modified with polymer was developed for such detection. First, the poly(4‐aminophenol) film was electrochemically deposited on a graphite electrode. Afterward, an S. pneumoniae‐specific oligonucleotide (Strep1), isolated from conserved regions of the bacterial genome, was immobilized onto the modified electrode surface and used for the test with complementary target oligonucleotide (Strep2) or genomic DNA. The genosensor was evaluated using electrochemical techniques and atomic force microscopy. Poly(4‐aminophenol) film caused an increase in probe immobilization, monitoring the guanine oxidation peak. The detection limits obtained using differential pulse voltammetry and electrochemical spectroscopy impedance were 54 and 28 ng mL^?1, respectively. The novel genosensor was efficient for the immobilization and detection of S. pneumoniae genomic DNA. POLYM. ENG. SCI., 58:1308–1314, 2018. © 2017 Society of Plastics Engineers     

Electrochemical synthesis of polymer based on 4-(2-furyl) benzenamine: Electrochemical properties,characterization and applications

4-(2-Furyl) benzenamine (FBA), was successfully synthesized by a simple method including substitution of furan on p-nitroaniline followed by reduction of nitro group. Structure of the synthesized monomer was verified using IR, ¹H NMR and GC–MS techniques. Corresponding poly(4-(2-furyl) benzenamine) (PFBA) was electrochemically synthesized in acidic aqueous and organic solutions by cyclic potential sweep method. Characterization of the resulting polymer was performed by cyclic voltammetry (CV), IR, UV–vis spectroscopy, and scanning electron microscopy (SEM). Effect of solvent on the electroactivity of the polymer modified electrode was investigated. The HOMO, LUMO levels and band gap energies of the doped and undoped form of the PFBA were calculated using UV–vis and CV data. The electrochromic properties and corrosion behavior of PFBA were studied. The electrochromic properties of the copolymer film, electrochemically coated on transparent conductive oxide, corroborate multi-color electrochromic behavior of the polymer whenever the applied potential was switched from reducing (yellow) to oxidizing status (green). The FBA polymer was found to exhibit enhanced corrosion protection effect on steel electrode in comparison with corresponding polyaniline (PANI) and polyfuran (PFu) homopolymers based on series of electrochemical measurements in 3.5 wt% NaCl electrolyte solutions.     

Preparation of block copolymers via metal‐free visible‐light‐induced ATRP for the detection of lead ions

Polyacrylamide‐b‐poly(methacrylic acid) was prepared on the surface of Au electrode (Au/PAM/PMAA) for Pb²⁺ ion electrochemical sensing via metal‐free visible‐light‐induced atom transfer radical polymerization, which was very simple, convenient, and environmentally friendly. Au/PAM/PMAA was carefully examined by cyclic voltammetry, electrochemical impedance spectroscopy, and X‐ray photoelectron spectroscopy. Further, Au/PAM/PMAA was successfully used for the determination of Pb²⁺ ion by differential pulse anodic stripping voltammetry. Under the optimal conditions, a linear response from 1.0 × 10^?11 to 1.0 × 10^?4 mol/L with detection limit of 2.5 × 10^?12 mol/L (S/N = 3) was achieved from the results of experiments. Comparing with similar Pb²⁺ sensors, the broader linear range and lower detection limit suggested the promising prospect of Au/PAM/PMAA. In a word, the work of this article had an important significance for the polymer‐modified electrodes and the sensitive detection of Pb²⁺. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45863.