The cyclic voltammetry(CV) and the square wave technique were used for the investigations of thallium(Ⅰ) underpotential deposition(UPD) on the silver electrode. A solution of 10 \{mmol/L\} HClO 4+10 mmol/L NaCl was s...The cyclic voltammetry(CV) and the square wave technique were used for the investigations of thallium(Ⅰ) underpotential deposition(UPD) on the silver electrode. A solution of 10 \{mmol/L\} HClO 4+10 mmol/L NaCl was selected as the supporting electrolyte. The calibration plots for Tl(Ⅰ) concentration in the range of 2×10 -9 -1×10 -7 mol/L were obtained. The detection limit was 5×10 -10 mol/L. For the solutions of 4 0×10 -9 mol/L thallium added before the urine sample pretreatment procedure, the average recovery was 105 6% with a relative standard deviation(RSD) of 15 5%.展开更多
A PCV-modified electrode was simply prepared by dip-coating a pyrolytic graphite electrode in a NaAc-HAc buffer solution of PCV. The peak currents of differential pulse voltammograms (DPV) decrease with the addition o...A PCV-modified electrode was simply prepared by dip-coating a pyrolytic graphite electrode in a NaAc-HAc buffer solution of PCV. The peak currents of differential pulse voltammograms (DPV) decrease with the addition of Al and the peak potentials remain the same. The decreasing of Delta i(p) is linear with Al concentration in the range of 1 x 10(-8) similar to 1 x 10(-7) mol/L. The detection limit is 5 x 10(-9) mol/L and the relative standard deviation for 4 x 10(-8) mol/L Al is 2.9% (n=8). No serious interference was found. The determination of Al in water samples is reported.展开更多
An electrochemical method for the simultaneous determination of lead(II) and Cadmium(II) with a calix[6]arene modified carbon paste electrode (CPE) has been developed. Pb2+ and Cd2+ were accumulated at the surface of ...An electrochemical method for the simultaneous determination of lead(II) and Cadmium(II) with a calix[6]arene modified carbon paste electrode (CPE) has been developed. Pb2+ and Cd2+ were accumulated at the surface of the modified electrode via formation of chemical complexes with calix[6]arene, and reduced at 1.40 V. During the following anodic potential sweep, reduced lead and cadmium were oxidized, and two well-defined striping peaks appeared at about ?0.60 V and ?0.84 V. Compared with a bare carbon paste electrode, the calix[6]arene modified CPE greatly improves the sensitivity of determining lead and cadmium. The stripping peak currents change linearly with the concentration of Pb2+ 3.0×10?8–8.0×10?6 mol·L?1 and with that of Cd2+ 6.0×10?8–1.0×10?5 mol ·L?1. The detection limits of Pb2+ and Cd2+ are found to be 8.0×10?9 mol·L?1 and 2.0×10?8 mol·L?1, respectively. The modified carbon paste electrode was applied to determine trace levels of lead and cadmium in water samples. Comparing with that of atomic absorption spectrometry, the results suggests that the calix[6]arene modified CPE has great potential for the practical sample analysis. Key words lead(II) - cadmium(II) - calix[6]arene - differential pulse stripping voltammetry - chemically modified electrode CLC number O 657.15 Foundation item: Supported by the National Natural Science Foundation of China (60171023)Biography: JI Xiao-bo (1980-), male, Master, research direction: electroanalytical chemistry.展开更多
An imidazole modified silver electrode is prepared by immersing the substrate silver electrode in a 2% imidazole solution of ethanol at 50°C for 10 min. The modified electrode is men swept in a cytochrome c solut...An imidazole modified silver electrode is prepared by immersing the substrate silver electrode in a 2% imidazole solution of ethanol at 50°C for 10 min. The modified electrode is men swept in a cytochrome c solution and the modified layer takes off because the modified electrode is very unstable. Although the amount of the silver-imidazole complex is very small compared with the amount of cytochrome c in the protein solution, it greatly facilitates redo reactions involving the biomacromolecules.展开更多
The chemically modified electrode (CME) which was constructed by covalent attaching erythromycin (ERM) to the glassy carbon (GC) surface was investigated in Tris-HCl buffer (pH=6.0) by cyclic voltammetry (CV) and diff...The chemically modified electrode (CME) which was constructed by covalent attaching erythromycin (ERM) to the glassy carbon (GC) surface was investigated in Tris-HCl buffer (pH=6.0) by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). In the potential range of -0.5～0.4V, CME yields a pair of stable redox wave. It is the carbonyl group of the ERM molecule immobilized on the GC surface that undergoes two electron redox process involving two protons. The interaction of CME with DNA was also studied by DPV. The CME shows the same interaction with DNA as that in the solution. And the result was proved by fluorescence.展开更多
A silver electrode was anodized in lowly concentrated potassium chloride solution almost under the steady state to generate a deposit of silver chloride on the electrode, and the deposit was cathodically stripped by l...A silver electrode was anodized in lowly concentrated potassium chloride solution almost under the steady state to generate a deposit of silver chloride on the electrode, and the deposit was cathodically stripped by linear potential scan to evaluate the reduction charge. Then the oxidation charge was larger than the reduction one. Since the equality was valid for long term chronocoulometry at the double potential step, the inequality is not due to any irreversibility of electrode reactions, but can be attributed to the process of the cathodic potential scan. A reason for the inequality is the negative charge of the capacitance involved in the electrode reaction, which has been observed in simple, dissolved redox species like a ferrocenyl derivative. The negative capacitive currents are conspicuous for high concentrations of redox species on the electrode because they result from the orientation of the dipoles of the redox species coupled with counterion, of which direction is opposite to that of the solvent dipoles. If a silver chloride film was thin enough to be regarded as a monolayer, we found that half of the cathodic stripping charge should be lost by the negative capacitance.展开更多
A novel differential pulse anodic stripping voltammetry for the determination of trace amounts of lead, using a biomacromolecule heparin drop-coated modified glassy carbon electrode, has been described. Pb2+ was depos...A novel differential pulse anodic stripping voltammetry for the determination of trace amounts of lead, using a biomacromolecule heparin drop-coated modified glassy carbon electrode, has been described. Pb2+ was deposited on the surface of a heparin-modified electrode at -1.0 V (vs. SCE) via forming Pb2+-heparin and subsequent re-duction at the electrode. In the following step, Pb-heparin was oxidized, and voltammograms were recorded by scanning the potential in a positive direction. Conditions were optimized with respect to the pH of the medium, the mass of drop-coated heparin, accumulation potential and accumulation time. The peak current was proportional to the Pb2+ concentration in the range of 2.0×10-9 to 7.0×10-7 mol/L. The detection limit was 3.0×10-10 mol/L. The relative standard deviation was 4.83% for 1.0×10-8 mol / L Pb2+ (n=10). The developed method has been applied to the determination of Pb2+ in water samples with satisfactory results.展开更多
The electrochemical behavior of the film of single wall carbon nanotube(SWNT) functionalized with carboxylic acid group was studied extensively at the glassy carbon(GC) electrode. One stable couple of waves correspond...The electrochemical behavior of the film of single wall carbon nanotube(SWNT) functionalized with carboxylic acid group was studied extensively at the glassy carbon(GC) electrode. One stable couple of waves corresponding to the redox of the carboxylic acid group, which was supported by the IR experiments, was observed. The electrode process involved four electrons, while the rate determining step was a one-electron reduction. The SWNT film modified electrode showed nice electrocatalytic behaviors toward the oxidations of some biomolecules such as dopamine, epinephrine and ascorbic acid.展开更多
文摘The cyclic voltammetry(CV) and the square wave technique were used for the investigations of thallium(Ⅰ) underpotential deposition(UPD) on the silver electrode. A solution of 10 \{mmol/L\} HClO 4+10 mmol/L NaCl was selected as the supporting electrolyte. The calibration plots for Tl(Ⅰ) concentration in the range of 2×10 -9 -1×10 -7 mol/L were obtained. The detection limit was 5×10 -10 mol/L. For the solutions of 4 0×10 -9 mol/L thallium added before the urine sample pretreatment procedure, the average recovery was 105 6% with a relative standard deviation(RSD) of 15 5%.
文摘A PCV-modified electrode was simply prepared by dip-coating a pyrolytic graphite electrode in a NaAc-HAc buffer solution of PCV. The peak currents of differential pulse voltammograms (DPV) decrease with the addition of Al and the peak potentials remain the same. The decreasing of Delta i(p) is linear with Al concentration in the range of 1 x 10(-8) similar to 1 x 10(-7) mol/L. The detection limit is 5 x 10(-9) mol/L and the relative standard deviation for 4 x 10(-8) mol/L Al is 2.9% (n=8). No serious interference was found. The determination of Al in water samples is reported.
文摘An electrochemical method for the simultaneous determination of lead(II) and Cadmium(II) with a calix[6]arene modified carbon paste electrode (CPE) has been developed. Pb2+ and Cd2+ were accumulated at the surface of the modified electrode via formation of chemical complexes with calix[6]arene, and reduced at 1.40 V. During the following anodic potential sweep, reduced lead and cadmium were oxidized, and two well-defined striping peaks appeared at about ?0.60 V and ?0.84 V. Compared with a bare carbon paste electrode, the calix[6]arene modified CPE greatly improves the sensitivity of determining lead and cadmium. The stripping peak currents change linearly with the concentration of Pb2+ 3.0×10?8–8.0×10?6 mol·L?1 and with that of Cd2+ 6.0×10?8–1.0×10?5 mol ·L?1. The detection limits of Pb2+ and Cd2+ are found to be 8.0×10?9 mol·L?1 and 2.0×10?8 mol·L?1, respectively. The modified carbon paste electrode was applied to determine trace levels of lead and cadmium in water samples. Comparing with that of atomic absorption spectrometry, the results suggests that the calix[6]arene modified CPE has great potential for the practical sample analysis. Key words lead(II) - cadmium(II) - calix[6]arene - differential pulse stripping voltammetry - chemically modified electrode CLC number O 657.15 Foundation item: Supported by the National Natural Science Foundation of China (60171023)Biography: JI Xiao-bo (1980-), male, Master, research direction: electroanalytical chemistry.
基金Project supported by the National Natural Science Foundation of China (No. 29575199) and the Natural Science Foundation of Jiangsu Province (Nos. BJ97310 and BS98082).
文摘An imidazole modified silver electrode is prepared by immersing the substrate silver electrode in a 2% imidazole solution of ethanol at 50°C for 10 min. The modified electrode is men swept in a cytochrome c solution and the modified layer takes off because the modified electrode is very unstable. Although the amount of the silver-imidazole complex is very small compared with the amount of cytochrome c in the protein solution, it greatly facilitates redo reactions involving the biomacromolecules.
文摘The chemically modified electrode (CME) which was constructed by covalent attaching erythromycin (ERM) to the glassy carbon (GC) surface was investigated in Tris-HCl buffer (pH=6.0) by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). In the potential range of -0.5～0.4V, CME yields a pair of stable redox wave. It is the carbonyl group of the ERM molecule immobilized on the GC surface that undergoes two electron redox process involving two protons. The interaction of CME with DNA was also studied by DPV. The CME shows the same interaction with DNA as that in the solution. And the result was proved by fluorescence.
文摘A silver electrode was anodized in lowly concentrated potassium chloride solution almost under the steady state to generate a deposit of silver chloride on the electrode, and the deposit was cathodically stripped by linear potential scan to evaluate the reduction charge. Then the oxidation charge was larger than the reduction one. Since the equality was valid for long term chronocoulometry at the double potential step, the inequality is not due to any irreversibility of electrode reactions, but can be attributed to the process of the cathodic potential scan. A reason for the inequality is the negative charge of the capacitance involved in the electrode reaction, which has been observed in simple, dissolved redox species like a ferrocenyl derivative. The negative capacitive currents are conspicuous for high concentrations of redox species on the electrode because they result from the orientation of the dipoles of the redox species coupled with counterion, of which direction is opposite to that of the solvent dipoles. If a silver chloride film was thin enough to be regarded as a monolayer, we found that half of the cathodic stripping charge should be lost by the negative capacitance.
基金Project supported by the National Natural Science Foundation of China (No. 20377007).
文摘A novel differential pulse anodic stripping voltammetry for the determination of trace amounts of lead, using a biomacromolecule heparin drop-coated modified glassy carbon electrode, has been described. Pb2+ was deposited on the surface of a heparin-modified electrode at -1.0 V (vs. SCE) via forming Pb2+-heparin and subsequent re-duction at the electrode. In the following step, Pb-heparin was oxidized, and voltammograms were recorded by scanning the potential in a positive direction. Conditions were optimized with respect to the pH of the medium, the mass of drop-coated heparin, accumulation potential and accumulation time. The peak current was proportional to the Pb2+ concentration in the range of 2.0×10-9 to 7.0×10-7 mol/L. The detection limit was 3.0×10-10 mol/L. The relative standard deviation was 4.83% for 1.0×10-8 mol / L Pb2+ (n=10). The developed method has been applied to the determination of Pb2+ in water samples with satisfactory results.
文摘The electrochemical behavior of the film of single wall carbon nanotube(SWNT) functionalized with carboxylic acid group was studied extensively at the glassy carbon(GC) electrode. One stable couple of waves corresponding to the redox of the carboxylic acid group, which was supported by the IR experiments, was observed. The electrode process involved four electrons, while the rate determining step was a one-electron reduction. The SWNT film modified electrode showed nice electrocatalytic behaviors toward the oxidations of some biomolecules such as dopamine, epinephrine and ascorbic acid.
