Gas Sensor Devices Obtained by Ink-jet Printing of Polyaniline Suspensions

We report on the fabrication process of a sensing device obtained by ink-jet printing of polyaniline suspension on alumina substrates. We optimized the inkjet parameters (amplitude and duration of jetting impulse, jetting frequency, substrate velocity) to obtain thin polyaniline lines as sensitive layers and we analyzed the morphology of PANI lines on substrate. Device response towards ammonia are also discussed and compared with reference device obtained by spin-coating.     

A polypyrrole-based amperometric ammonia sensor

An ammonia sensor is described in this work. The sensing membrane is a thin layer of oxidized polypyrrole (PPy) on a platinum substrate. This sensor is used as the working electrode in a conventional three-electrode system for amperometric measurement of ammonia in aqueous solutions in the potential range of + 0.2 to + 0.4 V (vs. Ag/AgCl). Contact with ammonia causes a current to flow through the electrode. This current is proportional to the concentration of free ammonia in the solution and ammonium ions do not contribute to the measured signal. The signal is due to reduction of PPy by ammonia with subsequent oxidation of PPy by the external voltage source. The sensor is able to detect ammonia reproducibly at the muM level. The main interference is the doping effect of small anions such as Cl(-) and NO(3)(-), also giving a response on PPy at the mM level. This anionic response can, to a certain degree, be reduced by covering the polymer surface with dodecyl sulfate. The sensor gradually loses its activity when exposed to ammonia concentrations greater than 1 mM. The sensor has been tested by the flow injection analysis technique.     

Amperometric methylene blue-mediated sensor highly sensitive to hydrogen peroxide based on a composite membrane of regenerated silk fibroin and poly-vinyl alcohol as immobilization matrix for horseradish peroxidase

Horseradish peroxidase (HRP) was effectively entrapped in a novel composite membrane of poly-vinyl alcohol and regenerated silk fibroin, and IR was employed to provide a useful insight into the structure of the composite membrane. A methylene bluemediated sensor highly sensitive to hydrogen peroxide was constructed, which was based on the immobilization of HRP in the composite membrane. Cyclic voltammetry and amperometric measurement were utilized to demonstrate the feasibility of electron communication between immobilized HRP and a glassy carbon electrode in the bioelectrocatalytic reduction of hydrogen peroxide via methylene blue. Performance and characteristics of the sensor were evaluated with regard to response time, detection limit, selectivity, and dependence on temperature and pH as well as operating and storage stability. The sensor possesses a variety of characteristics including high sensitivity, rapid response time and a low detection limit of 0.1 μmol/L.     

A non-enzymatic sensor for hydrogen peroxide based on polyaniline, multiwalled carbon nanotubes and gold nanoparticles modified Au electrode

We describe the construction of a polyaniline (PANI), multiwalled carbon nanotubes (MWCNTs) and gold nanoparticles (AuNPs) modified Au electrode for determination of hydrogen peroxide without using peroxidase (HRP). The AuNPs/MWCNT/PANI composite film deposited on Au electrode was characterized by Scanning Electron Microscopy (SEM) and electrochemical methods. Cyclic voltammetric (CV) studies of the electrode at different stages of construction demonstrated that the modified electrode had enhanced electrochemical oxidation of H(2)O(2), which offers a number of attractive features to develop amperometric sensors based on split of H(2)O(2). The amperometric response to H(2)O(2) showed a linear relationship in the range from 3.0 μM to 600.0 μM with a detection limit of 0.3 μM (S/N = 3) and with high sensitivity of 3.3 mA μM(-1). The sensor gave accurate and satisfactory results, when employed for determination of H(2)O(2) in milk and urine.     

Carbon nanoparticles-induced formation of polyaniline nanofibers and their subsequent decoration with Ag nanoparticles for nonenzymatic H2O2 detection

The present communication reports on the preparation of polyaniline nanofibers (PANINFs) by chemical oxidative polymerization of aniline under rapid stirring using ammonium persulfate as the oxidant in acidic aqueous media in the presence of carbon nanoparticles. The subsequent treatment of such nanofiber with a AgNO₃ aqueous solution leads to in situ chemical reduction of Ag⁺ on them to form Ag nanoparticle-decorated PANINFs. The resultant composites show good catalytic activity toward the reduction of H₂O₂. An effective enzymeless H₂O₂ sensor based on such composites is also constructed. It exhibits a fast amperometric response time 2 s, and it has a linear detection range from 0.1 to 60 mM and detection limit of 0.9 μM at a signal-to-noise ratio of 3, respectively.     

Polyaniline Film Based Amperometric pH Sensor Using A Novel Electrochemical Measurement System

A polyaniline based amperometric pH sensor has been developed using a novel electrochemical measurement system. A polyaniline film (PANI) coated pencil graphite electrode (PGE) is connected in series between the working and counter electrodes of a potentiostat, and immersed in the solution together with a reference electrode. When an external potential is applied, the resulting current varies with the solution pH, which provides the basis for the amperoemtric pH sensor. Equations describing the measurement principle are presented. Based on pH dependent emeraldine salt–emeraldine base transition of PANI film, the pH sensor exhibits high stability, accuracy, selectivity, sensitivity and a short time.     

Optimisation and characterisation of biosensors based on polyaniline

With lower limits of detection and increased stability constantly being demanded of biosensor devices, characterisation of the constituent layers that make up the sensor has become unavoidable, since this is inextricably linked with its performance. This work describe the optimisation and characterisation of two aspects of sensor performance: a conductive polymer layer (polyaniline) and the immobilised protein layer. The influence of the thickness of polyaniline films deposited electrochemically onto screen-printed electrode surfaces is described in this work in terms of its influence on a variety of amperometric sensor performance characteristics: time to reach steady state, charging current, catalytic current, background current and signal/background ratios. The influence of polymer film thickness on the conductivity and morphology of finished films is also presented.

An electrostatic method of protein immobilisation is used in this work and scanning electron microscopy in conjunction with gold-labelled antibodies and back-scattered electron detection has enabled the direct visualisation of individual groups of proteins on the sensor surface. Such information can provide an insight into the performance of sensors under influence of increasing protein concentrations.     

Voltammetric behavior and ion chromatographic detection of nitrite at a dispersed platinum glassy carbon electrode

Cyclic voltammetry was used to investigate the electrochemical behavior of nitrite at a platinum-modified glassy carbon electrode (Pt-CME) in phosphate buffer (pH 4.5). Experiments in flow injection analysis and ion-chromatography (IC) were performed to characterize the electrode as an amperometric sensor for the determination of nitrite ions. The effects of several common interferences on the amperometric signal were estimated. The electrode stability, precision, limit of detection, and linear range were evaluated at a constant applied potential of 1.1 V. Calibration plots were linear from 0.03 μM to 0.5 mM with a slope of about 21 μA/mM and a correlation coefficient of 0.9987. The limit of detection (LOD) was 15 nM (0.7 ppb) in a 100 μL injection. The electrode response was sufficiently stable: over 6 h of operating time a 2.8% signal loss was observed. The determination of nitrite in milk and pear juices was achieved by IC and the relevant results were compared with those obtained with a standard spectrophotometric method.     

Amperometric methylene blue-mediated sensor highly sensitive to hydrogen peroxide based on a composite membrane of regenerated silk fibroin and poly-vinyl alcohol as immobilization matrix for horseradish peroxidase

 Horseradish peroxidase (HRP) was effectively entrapped in a novel composite membrane of poly-vinyl alcohol and regenerated silk fibroin, and IR was employed to provide a useful insight into the structure of the composite membrane. A methylene blue-mediated sensor highly sensitive to hydrogen peroxide was constructed, which was based on the immobilization of HRP in the composite membrane. Cyclic voltammetry and amperometric measurement were utilized to demonstrate the feasibility of electron communication between immobilized HRP and a glassy carbon electrode in the bioelectrocatalytic reduction of hydrogen peroxide via methylene blue. Performance and characteristics of the sensor were evaluated with regard to response time, detection limit, selectivity, and dependence on temperature and pH as well as operating and storage stability. The sensor possesses a variety of characteristics including high sensitivity, rapid response time and a low detection limit of 0.1 μmol/L. Received: 10 January 1996/Revised: 20 March 1996/Accepted: 25 March 1996     

Amperometric Determination of Cholesterol-Reducing Drug,Ezetimibe, Using Glassy Carbon Electrode Modified with Multiwalled Carbon Nanotubes and Sodium Dodecylsulfate

A simple and sensitive electrochemical method is described for the determination of the cholesterol-reducing drug ezetimibe in aqueous solution. A glassy carbon electrode, modified with multiwalled carbon nanotubes and sodium dodecylsulphate was used as the working electrode. Ezetimibe yields a well-defined anodic peak at the surface of the electrode in an aqueous solution of pH 13. A linear amperometric calibration curve was obtained in the range of 1.2–78 μM (0.5–32.0 μg/mL) of ezetimibe, with a sensitivity of 88.6 nA/μM and a detection limit of 300 nM (0.12 μg/mL). The sensor was applied successfully to the determination of ezetimibe in pharmaceutical preparations.     

Operational parameters of voltammetric high-performance liquid chromatographic detectors with copper electrodes and application to a determination of some fodder biofactors

Two versions of an amperometric detector with a copper working electrode have been constructed and tested for high-performance liquid chromatography (HPLC). The performance of the detectors was studied using selected amino acids. The dependence of the detector response on the mobile phase flow-rate was studied in the range common in both macro- and microcolumn HPLC (5 microliter/min to 1.0 ml/min). It has been found that the detection sensitivity generally increases with decreasing flow-rate, i.e., the detector response is governed by the rate of the complexation reaction between the cupric ions and the solutes. This fact makes amperometric detection with a copper electrode especially useful for microcolumn separations. For all 20 amino acids studied, calibration curve parameters and detection limits have been determined; the latter vary from 0.4 to 18 ng in the injected volume. The amino acids can also be sensitively detected in a medium of 0.1-1.0 M ammonia, which is promising for the use of strong anion exchangers in amino acid separations. Choline can also be detected at a copper electrode, with a detection limit of 40 ng. An HPLC method with amperometric detection at a copper electrode has been developed for the determination of lysine, methionine and choline in fodder biofactors.     

Reagentless amperometric biosensor highly sensitive to hydrogen peroxide based on the incorporation of Meldola Blue, fumed-silica and horseradish peroxidase into carbon paste

 A reagentless amperometric sensor highly sensitive to H₂O₂ has been prepared by incorporating fumed silica, horseradish peroxidase (HRP) and Meldola Blue into carbon paste. The efficient mediating ability to shift electrons between HRP and the carbon paste electrode via Meldola Blue was investigated by cyclic voltammetric and amperometric measurements. Reproducibility, response time, detection limit, selectivity and effects of applied potential, temperature and pH on the response of the sensor are reported. The high sensitivity of the sensor with a detection limit of 0.1 μmol/l arose from the high efficiency of the bioelectrocatalytic reduction of hydrogen peroxide via HRP and Meldola Blue. The dependence of the Michaelis-Menten constant on the applied potential and the mediator concentration has been investigated and the results are presented. Received: 20 December 1995/Revised: 13 March 1996/Accepted: 16 March 1996     

Amperometric sensor for L-ascorbic acid determination based on MnO2 bulk modified screen printed electrode

A simple biosensor constructed by bulk-modification of carbon ink with manganese dioxide as a mediator was investigated for its ability to serve as amperometric detector for L-ascorbic acid in hydrodynamic mode. The sensor could be operated at pH 5.0 (0.05 M phosphate buffer) and exhibited excellent reproducibility and stability. Optimization of measurement parameters such as applied working potential and pH value were studied in detail. The screen printed electrode exhibited a linear amperometric increase with the concentration of L-ascorbic acid from 50 mg L(-1) to 250 mg L(-1) and gave a (LOD = 3sigma) detection limit of 0.2 mg L(-1) (1.172 micromol L(-1)). The manganese dioxide modified screen printed electrode shows long term stability.     

Amperometric sensor for detection of bisphenol A using a pencil graphite electrode modified with polyaniline nanorods and multiwalled carbon nanotubes

We report on a simple and highly sensitive amperometric method for the determination of bisphenol A (BPA) using pencil graphite electrodes modified with polyaniline nanorods and multiwalled carbon nanotubes. The modified electrodes display enhanced electroactivity for the oxidation of BPA compared to the unmodified pencil graphite electrode. Under optimized conditions, the sensor has a linear response to BPA in the 1.0 and 400?μM concentration range, with a limit of detection of 10?nM (at S/N?=?3). The modified electrode also has a remarkably stable response, and up to 95 injections are possible with a relative standard deviation of 4.2% at 100?μM of BPA. Recoveries range from 86 to 102% for boiling water spiked with BPA from four brands of baby bottles.

Inkjet printed Prussian blue films for hydrogen peroxide detection

An inkjet printing method is described to fabricate hydrogen peroxide (H(2)O(2)) sensors. Insoluble Prussian blue (PB) nanoparticles were dispersed in aqueous solvent, and were printed on screen printed carbon electrodes with a piezoelectric inkjet printer for H(2)O(2) detection. The electrochemical behavior of the printed sensors was studied by using cyclic voltammetry and chronoamperometry. The printed sensors showed great electrocatalytic activity toward H(2)O(2) and can be used for amperometric detection of H(2)O(2). The calibration curves for H(2)O(2) determination showed a linear range from 0.02 to 0.7 mM with a sensitivity of 164.82 μA M(-1) cm(-2) for the printed PB film. The results showed the feasibility of applying inkjet printing technology on surface modification; the results also provide an alternative way for manufacturing electrochemical sensors.     

Sol-gel-derived carbon ceramic electrode containing 9,10-phenanthrenequinone, and its electrocatalytic activity toward iodate

9,10-Phenanthrenequinone (PQ) supported on graphite powder by adsorption was dispersed in propyltrimethoxysilane-derived gels to yield a conductive composite which was used as electrode material to fabricate a PQ-modified carbon ceramic electrode. In this configuration, PQ acts as a catalyst, graphite powder guarantees conductivity by percolation, the silicate provides a rigid porous backbone, and the propyl groups endow hydrophobicity and thus limit the wetting region of the modified electrode. Square-wave voltammetry was exploited to investigate the pH-dependent electrochemical behavior of the composite electrode and an almost Nernstian response was obtained from pH 0.42 to 6.84. Because the chemically modified electrode can electrocatalyze the reduction of iodate in acidic aqueous solution (pH 2.45), it was used as an amperometric sensor for the determination of iodate in table salt. The advantages of the electrode are that it can be polished in the event of surface fouling, it is simple to prepare, has excellent chemical and mechanical stability, and the reproducibility of surface-renewal is good.     

铁酞菁/氮掺杂石墨烯复合物的电化学传感研究

本文用快速简便的方法制备了铁酞菁/氮掺杂石墨烯（FePc/N-G）修饰电极,用于定量检测半胱氨酸. 采用电化学方法对修饰电极的性能进行了表征,结果表明氮掺杂石墨烯负载铁酞菁修饰电极对半胱氨酸具有更宽的线性响应范围和较高的灵敏度.     

Methylene green-mediated sensor highly sensitive to hydrogen peroxide based on entrapment of horseradish peroxidase in composite membrane of regenerated silk fibroin and poly(vinyl alcohol)

Introduction The detection and quantitative determination of hydrogen peroxide play importantrole in several fields including biochemistry and environmental chemistry.A highlysensitive H202 sensor is useful to fabricate sensor for various substances by combiningit with hydrogen peroxide—producing oxidases.‘Although electrochemical detection ofH202 has been made via its oxidation or reduction at a variety of electrode materials,these electrodes are susceptible to the interference from electr…     

Amperometric sensor for L-ascorbic acid determination based on MnO2 bulk modified screen printed electrode

A simple biosensor constructed by bulk-modification of carbon ink with manganese dioxide as a mediator was investigated for its ability to serve as amperometric detector for L-ascorbic acid in hydrodynamic mode. The sensor could be operated at pH 5.0 (0.05 M phosphate buffer) and exhibited excellent reproducibility and stability. Optimization of measurement parameters such as applied working potential and pH value were studied in detail. The screen printed electrode exhibited a linear amperometric increase with the concentration of ¶L-ascorbic acid from 50 mg L^–1 to 250 mg L^–1 and gave a (LOD = 3σ) detection limit of 0.2 mg L^–1 (1.172 μmol L^–1). The manganese dioxide modified screen printed electrode shows long term stability.     

二氧化锆/石墨烯复合材料对亚硝酸盐的电化学传感研究

制备了一种二氧化锆/还原氧化石墨烯(ZrO2NPs/rGO)复合材料修饰电极的亚硝酸盐电化学传感器,并成功用于亚硝酸盐的检测.采用循环伏安法和电流-时间曲线考察了修饰电极的电化学行为.实验结果表明,ZrO2NPs/rGO复合材料修饰电极对亚硝酸盐具有良好的电流响应.在最优实验条件下,电流-时间曲线中的电流响应信号与亚硝酸盐浓度在3.0×10Symbolm@@_7～1.0×10Symbolm@@_6 mol/L和1.0×10Symbolm@@_6～6.0×10Symbolm@@_6 mol/L的范围内呈良好的线性关系,检测限为1.0×10Symbolm@@_7 mol/L(S/N 3).该传感器灵敏性高、稳定性和重现性好.使用此传感器检测实际样品香肠中的亚硝酸盐的回收率为93.7％～110.4％,相对标准偏差为1.6％～2.1％.