Determination of trace amount of antimony (Ⅲ) by adsorption voltammetry on carbon paste electrode

A sensitive method is described for the determination of trace antimony based on the antimony-bromopyrogallol red (BPR) adsorption at a carbon paste electrode (CPE). Three steps were involved in the overall analysis: preconcentration,reduction and stripping. Optimal conditions were found to be an electrode containing 25% paraffin oil and 75% high purity graphite powder as working electrode;a 0.10 mol/L HCl solution containing 40 μmol/L BPR as accumulation medium;a 0.20 mol/L HCl solution as reduction and stripping electrolyte;accumulation time,150 s;reduction potential and time,-0.50 V,60 s;scan range from -0.50 to 0.20 V. Interferences by other ions were studied as well. The detection limit was found to be 0.5 nmol/L for 150 s preconcentration. The linear range was from 1.0 nmol/L to 0.50 μmol/L. Application of the proposed method to the determination of antimony in water and human hair samples gave good results.

Trace Determination of Scandium Using Adsorption Voltammetry of Mix-Polynuclear Complex of Scandium-Calcium-Alizarin Red S at Carbon Paste Electrode

A novel method was described for the determination of ultra trace amount of scandium based on the cathodic adsorptive voltammetry of the mix-polynuclear complex of scandium-calcium-alizarin red S at a carbon paste electrode (CPE). The 2nd-order derivative linear scan voltammograms of the adsorbed complex were recorded by model JP-303 polarographic analyzer from 0.0 to -1.0 V (vs. SCE). The experimental conditions of the working procedure were optimized. The results show that the complex can be adsorbed on the surface of the CPE, yielding one peak at -0.61 V, corresponding to the reduction of the alizarin red S in the mix-polynuclear complex at the electrode. The detection limit of Sc^(3+) is 1.0×10^(-10) mol·L^(-1) for 3 min of accumulation time. The procedure was successfully applied to the determination of trace amount of scandium in the sample ores.

Trace Determination of Zirconium(Ⅳ) by Anodic Adsorptive Voltammetry at a Carbon Paste Electrode

A new sensitive adsorptive voltammetric method was described for the determination of zirconium at a carbon paste electrode (CPE) in the presence of alizarin complexone (ALC). Optimal analytical conditions are: 1.0?0-6 or 5.0?0-7 mol/L ALC, 0. 20 mol/L HAC-NaAc (pH 4.3), accumulation for 60 s at 0 V (vs. SCE), and linear scanning from 0 V to 1.0 V at 250 mV/s. The peak potential of the complex is at 0.81 V. By using a model JP-303 polarographic analyzer, 2.0?0-10 mol/L (S/N=3) zirconium can be detected with a 90 s accumulation, when the 2nd-order derivative linear sweep technique is used, and the linear range is 6.0?0-10-2.0?0-8 mol/L (5.0?0-7 mol/L ALC) and 2.0?0-8-2.0?0-7 mol/L (1.0?0-6 mol/L ALC), respectively. The developed method was applied to the determination of trace zirconium in the ore samples with satisfactory results.

Electrochemical determination of vitamin C in the presence of uric acid by a novel TiO_2 nanoparticles modified carbon paste electrode

The electrochemical behavior of vitamin C（ascorbic acid or AA） is investigated on the surface of a carbon-paste electrode modified with TiO2 nanoparticles and 2,2＇-（1,2 butanediylbis（nitriloethylidyne））-bis-hydroquinone（BBNBH）.The prepared modified electrode showed an efficient catalytic role in the electrochemical oxidation of AA,leading to remarkable decrease in oxidation overpotential and enhancement of the kinetics of the electrode reaction.This modified electrode exhibits well-separated oxidation peaks for AA and uric acid（UA）.The modified electrode is successfully applied for the accurate determination of AA in pharmaceutical preparations.

Electrocatalytic oxidation of hydrazine on magnetic bar carbon paste electrode modified with benzothiazole and iron oxide nanoparticles: Simultaneous determination of hydrazine and phenol

A magnetic bar carbon paste electrode （MBCPE） modified with Fe3O4 magnetic nanoparticles （Fe3O4NPs） and 2‐（3,4‐dihydroxyphenyl） benzothiazole （DPB） for the electrochemical determina‐tion of hydrazine was developed. The DPB was firstly self‐assembled on the Fe3O4NPs, and the re‐sulting Fe3O4NPs/DPB composite was then absorbed on the designed MBCPE. The MBCPE was used to attract the magnetic nanoparticles to the electrode surface. Owing to its high conductivity and large effective surface area, the novel electrode had a very large current response for the electrocat‐alytic oxidation of hydrazine. The modified electrode was characterized by voltammetry, scanning electron microscopy, electrochemical impedance spectroscopy, infrared spectroscopy, and UV‐visible spectroscopy. Voltammetric methods were used to study the electrochemical behaviour of hydrazine on MBCPE/Fe3O4NPs/DPB in phosphate buffer solution （pH = 7.0）. The MBCPE/Fe3O4NPs/DPB, acting as an electrochemical sensor, exhibited very high electrocatalytic activity for the oxidation of hydrazine. The presence of DPB was found to reduce the oxidation potential of hydrazine and increase the catalytic current. The dependence of the electrocatalytic current on the hydrazine concentration exhibited two linear ranges, 0.1–0.4 μmol/L and 0.7–12.0 μmol/L, with a detection limit of 18.0 nmol/L. Additionally, the simultaneous determination of hydrazine and phe‐nol was investigated using the MBCPE/Fe3O4NPs/DPB electrode. Voltammetric experiments showed a linear range of 100–470 μmol/L and a detection limit of 24.3 μmol/L for phenol, and the proposed electrode was applied to the determination of hydrazine and phenol in water samples.

Electrocatalytic Oxidation of H_2 O_ 2 at a Carbon Paste Electrode Modified with a Nickel (Ⅱ)-5,11,17,23-Tetra-Tert-Butyl-25,27-Bis(Diethylcarbamoylmethoxy)Calix[4] Arene Complex and Its Application

Electrochemical behavior of a carbon paste electrode (CPE) modified with nickel(II)\|5, 11, 17, 23\|tetra\|tert\|butyl\|25, 27\|bis(diethylcarbamoylmethoxy)calix\arene (Ni(Ⅱ)\|L) complex and its electrocatalytic activity towards the oxidation of hydrogen peroxide were investigated by cyclic voltammetric technique in a 5.0×10 -2 mol/L NaClO 4+ 1.0×10 -3 mol/L NaOH solution. It was found that Ni(II)\|L acts as an effective catalyst for the oxidation of hydrogen peroxide. The modified electrode exhibited a linear response over a hydrogen peroxide concentrations in the range of 2.0×10 -6 \|1.0×10 -4 mol/L with a detection limit as low as 1.0×10 -6 mol/L. The relative standard deviation was 3.5% for 5 successive determinations of H 2 O 2 at 1.0×10 -5 mol/L. The modified electrode was used successfully in rainwater analysis.

Cyclam Modified Carbon Paste Electrode as a Potentiometric Sensor For Determination of Cobalt(Ⅱ) Ions

A new modified carbon paste electrode based on cyclam as a modifier was prepared for the determination of Co(Ⅱ) ions. The proposed electrode shows a Nernstian slope 28.4 mV per decade over a wide concentration range 5.0×10 -6_1.0×10 -1 mol/L of Co 2+ ions with detection limit 2.5×10 -6 mol/L. The sensor exhibits good selectivities for Co 2+ over a wide variety of other cations. It can be used as an indicator electrode in potentiometric titration of cobalt(Ⅱ) ions as well as in direct determination of cobalt(Ⅱ) ions in wastewater of acidic cobalt electroplating bath. The electrode shows Nernestian behavior in a solution of 25% ethanol.

Mixed Binder Carbon Paste Electrode for Quantitation of Isoniazid in Serum

This paper covers the construction and behaviour of a mixed binder carbon paste electrode system appropriate for the cathodic stripping voltammetric quantitation of iso-niazid. The mixed binder consisted of glycerol and liquid paraffin. At the mixed binder carbon paste electrodes in a pH 3.0 buffer solution, isoniazid showed two sensitive cathodic stripping voltammetric wave at-0. 75 V (p1) and-0. 88 V (p2) , respectively. The p2 can be used for the determination of trace amounts of isoniazid, the linear range of the peak current to the isoniazid concentration being from 5. 0×10-7 to 5.0×10-5 mol/L, and the limit of detection being 1. 0×10-7 mol/L with a relative standard deviation of 6. 0%(n=10). The proposed method was directly used to determine the drug in blood serum without the pretreatment of blood serum.

SBA-15 Modified Carbon Paste Electrode for Rapid cTnI Detection with Enhanced Sensitivity

A novel electrochemical immunoassay for cardiac troponin Ⅰ （cTnI） combining the concepts of the dual monoclonal antibody ＂sandwich＂ principle, the silver enhancement on the nano-gold particle, and the SBA-15 mesoporous modified carbon paste electrode （SBA-MCPE） is described. Four main steps were carried out to obtain the analytical signal, i.e., electrode preparation, immunoreaction, silver enhancement, and anodic stripping voltammetric detection. A linear relationship between the anodic stripping peak current and concentration of cTnI from 0.5 to 5.0 ng/mL and a limit of detection of 0.2 ng/mL of cTnI were obtained.

Gold Nanoparticle-based Layer-by-Layer Enhancement of DNA Hybridization Electrochemical Signal at Carbon Nanotube Modified Carbon Paste Electrode

Colloid gold nanoparticle-based layer-by-layer amplification approach was applied to enhance the electrochemical detection sensitivity of DNA hybridization at carbon nanotube modified carbon paste electrodes （CNTPEs）. Streptavidin was immobilized onto the surface of CNTPEs, and the conjugation of biotin labeled target oligonucle,otides to the above immobilized streptavidin was performed, followed by the hybridization of target oligonucleotides with the gold nanoparticle-labeled DNA probe and then the layer-by-layer enhanced connection of gold nanoparticles, on which oligonucleotides complementary to the DNA probe were attached, to the hybridization system. The differential pulse voltammetry （DPV） signal of total gold nanoparticles was monitored. It was found that the layer-by-layer colloidal gold DPV detection enhanced the sensitivity by about one order of magnitude compared with that of one-layer detection. One-base mismatched DNA and complementary DNA could be distinguished clearly.

Voltammetric Determination of Estrogens Based on the Enhancement Effect of Surfactant at Carbon Paste Electrode

Highly sensitive voltammetric method for the determination of estrogens, based on the enhancement effect of cetyltrimethylammonium bromide (CTAB) has been described. In the presence of CTAB, the oxidation peak currents of estrogens (estradiol, estrone, estriol, estradiol valerate and diethylstilbestrol) as the carbon paste electrode (CPE) increased significantly after open-circuit accumulation. The peak current was proportional to the concentration of estradiol over the range from 5×10?9 to 2.5×10?6 mol·L?1. The detection limit was 8×10?10 mol·L?1 at 6 min of accumulation. The total amounts of estrogens in the blood serums were determined and the average recovery was 104.92%. Under the conditions used, the electrode process of estradiol was examined the mechanism for peak current enhancement was also discussed.

Studies on Zeolite Modified Electrode(Ⅰ)─Ascorbic Acid Sensor Based on Carbon Paste Electrode Containing Fe(Ⅲ)Y Zeolite

A new ascorbic acid sensor constituted of carbon paste and Fe(Ⅲ)Y zeolite was studied.The characters of the sensor such as linear range. potential window、apparen Michaelis constant、response time、stability and accuracy wee investigated. The experimental results indicate that the analytical performance of the sensor is satisfactory.

Carbon Paste Electrodes for the Analysis of Some Agricultural Pollutants and Trace Metals

The present work is concerned with the voltammetric application of unmodified tricresyl phosphate carbon paste electrode （TCP-CPE） and in situ bismuth-film modified tricresyl phosphate-based carbon paste electrode （BiF-TCP-CPE）. The TCP-CPE was examined with the main objective of using it for the differential pulse voltammetric analysis of some neonicotinoid insecticides in aqueous Britton-Robinson buffer solution pH 7.0 as supporting electrolyte. After comparing the performance of the TCP-CPE with that of silicone oil carbon paste electrode, quantitative analysis of imidacloprid, thiamethoxam and clothianidin was performed in model solutions and real samples （river water and commercial insecticide formulations）. The in situ prepared BiF-TCP-CPE was tested for a simultaneous detection of selected heavy metal ions （Cd^2＋ and Pb^2＋） at a μg/dm^3 concentration level, using square wave anodic stripping voltammetric technique. The influence of different electrochemical pretreatments of the working electrode on the bismuth deposition and analyte signals were investigated. Film formation was studied at untreated, pre-cathodized and pre-anodized TCP-CPEs in the acetic buffer solution pH 4.6, containing 1 μg/cm^3 Bi （III）.

The attachment of Staphylococcus epidermidis on the surface of a carbon paste electrode at various positive potentials:The effect of pH,incubation time,and solid-medium type

The attachment of Staphylococcus epidermidis to the surface of carbon paste electrode (CPE) by applying positive potentials (50 - 600 mV) with regard of various buffer pH, cultivation time and solid-medium type was studied. The attachment process was analyzed by measuring the electric current derived from the dye (amido black) adsorbed on the vacant areas of CPE after attachment of microbial cells. The pH was not identified as a single main factor affecting the attachment (p > 0.05), however further insight revealed that the potentials applied had different effects on the microbial cells attachment. Both cultivation time and solid-medium type significantly affected the microbial attachment. Generally, increase of cultivation time up to 168 h resulted in increase of adhesion. Applying potentials 300, 400 and 200 mV resulted in the highest attachment process for bacteria cultivated for 24, 48 and 168 h, respectively. S. epidermidis cultivated on the blood agar and Baird-Parker agar plates showed the higher extent of attachment.

Trace detection of Ce^(3+) by adsorption strip voltammetry at a carbon paste electrode modified with ion imprinted polymers

To develop a convenient method for sensitive and selective determination of Ce3＋ in aqueous phase with complicated matrices, a carbon paste electrode（CPE） modified with ion imprinted polymers（IIPs） were fabricated. The polymers were prepared by precipitation polymerization using Ce3＋ as template, allyl phenoxyacetate（APA） as monomer, ethylene glycol dimethacrylate（EGDMA） as crosslinker and azobisisobutyronitrile（AIBN） as initiator under the molar ratio of Ce3＋, APA and EGDMA as 1：4：40, respectively. Ce3＋ was detected directly by differential pulse adsorptive stripping voltammetry（DPASV） and its oxidation peak appears at about 0.93 V. All parameters affecting the sensor＇s response are optimized and a calibration curve is plotted at a linear range of 1.0 × 10^（-6）-1.0 x 10^（-5） mol/L and 1.0×10^（-5）-2.0 × 10^（-4）mol/L with the detection limit of 1.5 × 10^（-7） mol/L. All other rare earth ions have no interference with the determination of Ce^（3＋） even at a concentration 500 times higher than that of Ce^（3＋）.This sensor was successfully applied to determination of Ce^（3＋） in two catalyst sample solutions with RSD≤3.3%（n = 5）and recoveries in the range of 99.2%-106.5% at our optimal conditions.

Electrochemical sensor for Cd2+ and Pb2+ detection based on nano-porous pseudo carbon paste electrode

An electrochemical sensor based on self-made nano-porous pseudo carbon paste electrode(nano-PPCPE)has been successfully developed,and used to detect Cd^2+ and Pb^2+.The experimental results showed that the electrochemical performance of nanoPPCPE is evidently better than both glassy carbon electrode(GCE)and pure carbon paste electrode(CPE).Then the prepared nano-PPCPE was applied to detect Cd^2+ and Pb^2+in standard solution,the results showed that the electrodes can quantitatively detect trace Cd^2+ and Pb^2+,which has great significance in electrochemical analysis and detection.The linear ranges between the target ions concentration and the D PASV current were from 0.1-3.0 μmol/L,0.05-4.0 μmol/L for Cd^2+ and Pb^2+,respectively.And the detection limits were 0.0780 μmol/L and 0.0292 μmol/L,respectively.Moreover,the preparation of the nano-PPCPE is cheap,simple and has important practical value.

CuO-nanoparticles modified carbon paste electrode for square wave voltammetric determination of lidocaine: Comparing classical and Box–Behnken optimization methodologies

In this research, copper oxide nanoparticles modified carbon paste electrode was developed for the voltammetric determination of lidocaine. The square wave voltammogram of lidocaine solution showed a well-defined peak between ＋0.5 and ＋1.5 V. Instrumental and chemical parameters influencing voltammetric response were optimized by both one at a time and Box–Behnken model of response surface methodology. The results revealed that there was no significant difference between two methods of optimization. The linear range was 1–2500 μmol L^-1（Ip= 0.11 C（LH）＋ 17.38, R^2= 0.999）. The LOD and LOQ based on three and ten times of the signal to noise（S/N） were 0.39 and 1.3 μmol L^-1（n = 10）,respectively. The precision of the method was assessed for 10 replicate square wave voltammetry（SWV）determinations each of 0.05, 0.5 and 1 μmol L^-1 of lidocaine showing relative standard deviations 4.1%,3.7% and 2.1%, respectively. The reliability of the proposed method was established by application of the method for the determination of lidocaine in two pharmaceutical preparations, namely injection and gel.

Inorganic-Organic Hybrid 18-Molybdodiphosphate Nanoparticles Bulk-modified Carbon Paste Electrode and Its Electrocatalysis

A kind of inorganic organic hybrid 18 molybdodiphosphate nanoparticles ([(C 4H 9) 4N] 6P 2Mo 18 O 62 ·4H 2O) was firstly used as a bulk modifier to fabricate a three dimensional chemically modified carbon paste electrode (CPE) by direct mixing. The electrochemical behavior of the solid nanoparticles dispersed in the CPE in acidic aqueous solution was characterized by cyclic and square wave voltammetry. The hybrid 18 molybdodiphosphate nanoparticles bulk modified CPE (MNP CPE) displayed a high electrocatalytic activity towards the reduction of nitrite, bromate and hydrogen peroxide. The remarkable advantages of the MNP CPE over the traditional polyoxometalates modified electrodes are their excellent reproducibility of surface renewal and high stability owing to the insolubility of the hybrid 18 molybdodiphosphate nanoparticles.

Carbon Paste Electrode Modified by Surfactant for Anodic Stripping Voltammetric Determination of Sulphadiazine

he present paper covers the construction and behaviour of a mixed binder car-bon paste electrode modified by surfactant system appropriate for the anodic strip-ping voltammetric quantitation of sulphadiazine. The mixed binder consisted ofglycerol and liquid paraffin. On this electrode in a PH 8. 20 buffer solution sulpha-diazine yields a sensitive anodic stripping voltammetric wave at 0. 82 V. It can beused for the determination of trace amounts of drug, the linear range of the peakcurrent to the sulphadiazine concentration being from 1. 0 x 10-7 to 5. 0 x 10-5mol/L, and the detection limit being 6. 6 x 10-9 mol/L with a relative standard de-viation of 2. 6% (n= 15).The proposed method was used to determine the drug inurine samples.

An Ionic Liquid Bulk-Modified Carbon Paste Electrode and Its Electrocatalytic Activity toward p-Aminophenol

An ionic liquid bulk-modified carbon paste electrode （M-CPE） has been fabricated by using 1-heptyl-3-methylimidazolium bromide as a modifier. Cyclic voltammetry （CV） and differential pulse voltammetry （DPV） were used to evaluate the electrocatalytic activity of the proposed electrode by choosing p-aminophenol （p-AP） as a model compound. Both at a bare carbon paste electrode （CPE） and the M-CPE, p-AP yielded a pair of redox peaks in 0.1 mol·L^-1 phosphate buffer solution （PBS, pH 7.0）. At the CPE, the peak-to-peak potential separation （AEp） was 0.233 V, while at the M-CPE the AEp was decreased to 0.105 V. Furthermore, the current response to p-AP at the M-CPE was 10.2 times of that at the CPE by DPV. The electron transfer rate constant （ks） ofp-AP at the M-CPE was 13.3 times of that at the CPE. Under the optimal condition, a linear dependence of the catalytic current versus p-AP concentration was obtained in the range of 2.0× 10^- 6 to 3.0× 10^- 4 mol·L^-1 with a detection limit of 6.0× 10^-7 mol·L^-1 by DPV. In addition, compared to other modified method the proposed electrode exhibited distinct advantages of simple prapartion, surface renewal, good reproducibility and good stability. It has been used to determine p-AP in simulated wastewater samples.