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 accu...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.展开更多
An Eastman-AQ/Ni(II)chemically modified electrode(CME) produced by“double coating steps”deposition of Eastman-AQ/Ni(II) film and Ni(II)-coating crystalline species onto glassy carbon instead of metallic nickel elect...An Eastman-AQ/Ni(II)chemically modified electrode(CME) produced by“double coating steps”deposition of Eastman-AQ/Ni(II) film and Ni(II)-coating crystalline species onto glassy carbon instead of metallic nickel electrode exhibited stable electrocatalytic oxidation of numerous ∝-hydrogen compounds including carbohydrates, amines and amino acids.Determination of glucose in FIA on the CME, the linear response concentration range was bstween 1.0×10^(-5) and 5.0×10^(-2) mol/L and the detection limit was 5.0×10^(-6)mol/L.The stability of the CME was adequate for routine quantitative application.展开更多
An electrode for uric acid has been prepared by using an iodide selective electrode with the uricase enzyme. The iodide selective electrode used was prepared from 10% TDMAI and PVC according to our previous study. The...An electrode for uric acid has been prepared by using an iodide selective electrode with the uricase enzyme. The iodide selective electrode used was prepared from 10% TDMAI and PVC according to our previous study. The enzyme was immobilized on the iodide electrode by holding it at pH 7 phosphate buffer for 20 min at room temperature. The H2O2 formed from the reaction of uric acid was determined from the decrease of iodide concentration that was present in the reaction cell. The potential change was linear in the 2 × 10-5 to 2 × 10-4 M uric acid concentration (3 - 34 mg uric acid/100ml blood) range. Uric acid contents of some blood samples were determined with the new electrode and consistency was obtained with a colorimetric method. The effects of pH, iodide concentration, the amount of enzyme immobilized and the operating temperature were studied. No interference of ascorbic acid, glucose and urea was observed.展开更多
Nowadays, modified electrodes with metal nanoparticles have appeared as an alternative for the electroanalysis of various compounds. In this study, gold nanoparticles（GNPs） were chosen as interesting metal nanoparti...Nowadays, modified electrodes with metal nanoparticles have appeared as an alternative for the electroanalysis of various compounds. In this study, gold nanoparticles（GNPs） were chosen as interesting metal nanoparticles for modifying carbon paste electrode（CPE）. GNPs and the gold nanoparticles-modified carbon paste electrode（GNPs/CPE） were characterized by UV–Vis spectroscopy, transmission electron microscopy（TEM） and scanning electron microscopy（SEM）. GNPs/CPE as a simple and sensitive electrode was used to study three important biological molecules： folic acid（FA）, uric acid（UA） and ascorbic acid（AA）. Square wave voltammetry（SWV） was used as an accurate technique for quantitative measurements. A good linear relation was observed between anodic peak current（ipa） and FA（5.2 × 10（-6）– 2.5 × 10（-5）M）, UA（1.2 × 10（-6）– 2.1 × 10（-5）M） and AA（1.2 × 10（-6）– 2.5 × 10（-5）M） concentrations in simultaneous determination of these molecules.展开更多
Standard electrode potentials E° of Ag-AgC1 electrode in molality scale and acidity constants of glyeine pK_1° at constant molality of NaCl (1.0 mol·kg^(-1)) in 5 and 15 mass% glucose-water mixed solven...Standard electrode potentials E° of Ag-AgC1 electrode in molality scale and acidity constants of glyeine pK_1° at constant molality of NaCl (1.0 mol·kg^(-1)) in 5 and 15 mass% glucose-water mixed solvents over a range of temperatures from 278.15 to 318.15 K were determined from precise emf measurements.The dependence of acidity constant on temperature is given as a function of the thermodynamic temperature T by an empirical equation, pK_1° =A_1(K/T)-A_2+A_3(T/K).The corresponding thermodynamic quantities of the first dissociation process of glycine were calculated and the effects of both tho solvent and the salt on them were also discussed.展开更多
A carbon paste electrode（CPE） chemically modified with multiwall carbon nanotubes and ferrocene（FC） was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine...A carbon paste electrode（CPE） chemically modified with multiwall carbon nanotubes and ferrocene（FC） was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine（CA） and folic acid（FA）.This modified electrode showed very efficient electrocatalytic activity for the anodic oxidation of CA.The peak current of differential pulse voltammograms of CA and FA increased linearly with their concentration in the ranges of 0.7-200μmol/L CA and 5.0- 700μmol/L FA.The detection limits for CA and FA were 0.3μmol/L and 2.0μmoI/L,respectively.The diffusion coefficient（D） and transfer coefficient（α） of CA were also determined.These conditions are sufficient to allow determination of CA and FA both individually and simultaneously.展开更多
In this study,Au nanoparticles/poly 5-[（2-hydroxynaphthalen-l-yl）diazenyl]isophthalic acid film modified glassy carbon electrode（AuNPs/poly（NDI）/GCE） has shown excellent electrocatalytic activity toward the oxid...In this study,Au nanoparticles/poly 5-[（2-hydroxynaphthalen-l-yl）diazenyl]isophthalic acid film modified glassy carbon electrode（AuNPs/poly（NDI）/GCE） has shown excellent electrocatalytic activity toward the oxidation of adrenaline（ADR）,paracetamol（PAC）,and tryptophan（Trp）.The bare glassy carbon electrode（GCE） fails to separate the oxidation peak potentials of these molecules,while the poly（NDI） film modified electrode can resolve them.Electrochemical impedance spectroscopy（EIS）indicates that the charge transfer resistance of the bare electrode decreases as 5-[（2-hydroxynaphthalen-l-yl）diazenyl]isophthalic acid is electropolymerized on the bare electrode.Furthermore,EIS exhibits enhancement of electron transfer kinetics between analytes and the electrode after electrodeposition of Au nanoparticles.Differential pulse voltammetry results show that the electrocatalytic current increases linearly in the ranges of 0.01-680.0 μmol L^-1 for ADR,0.05-498.0 μmol L^-1 for PAC,and 3.0-632.0 μmol L^-1 for Trp;with detection limits（S/N = 3） of 0.009 μmol L^-1,0.005 μmol L^-1,and 0.09 μmol L^-1 for ADR,PAC,and Trp,respectively.The proposed method has been successfully applied for simultaneous determination of ADR,PAC,and Trp in biological samples.展开更多
文摘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.
文摘An Eastman-AQ/Ni(II)chemically modified electrode(CME) produced by“double coating steps”deposition of Eastman-AQ/Ni(II) film and Ni(II)-coating crystalline species onto glassy carbon instead of metallic nickel electrode exhibited stable electrocatalytic oxidation of numerous ∝-hydrogen compounds including carbohydrates, amines and amino acids.Determination of glucose in FIA on the CME, the linear response concentration range was bstween 1.0×10^(-5) and 5.0×10^(-2) mol/L and the detection limit was 5.0×10^(-6)mol/L.The stability of the CME was adequate for routine quantitative application.
基金the Gazi University research fund for the financial support of this research.
文摘An electrode for uric acid has been prepared by using an iodide selective electrode with the uricase enzyme. The iodide selective electrode used was prepared from 10% TDMAI and PVC according to our previous study. The enzyme was immobilized on the iodide electrode by holding it at pH 7 phosphate buffer for 20 min at room temperature. The H2O2 formed from the reaction of uric acid was determined from the decrease of iodide concentration that was present in the reaction cell. The potential change was linear in the 2 × 10-5 to 2 × 10-4 M uric acid concentration (3 - 34 mg uric acid/100ml blood) range. Uric acid contents of some blood samples were determined with the new electrode and consistency was obtained with a colorimetric method. The effects of pH, iodide concentration, the amount of enzyme immobilized and the operating temperature were studied. No interference of ascorbic acid, glucose and urea was observed.
基金the Post-graduate Office of Guilan University(A-384579)for supporting
文摘Nowadays, modified electrodes with metal nanoparticles have appeared as an alternative for the electroanalysis of various compounds. In this study, gold nanoparticles（GNPs） were chosen as interesting metal nanoparticles for modifying carbon paste electrode（CPE）. GNPs and the gold nanoparticles-modified carbon paste electrode（GNPs/CPE） were characterized by UV–Vis spectroscopy, transmission electron microscopy（TEM） and scanning electron microscopy（SEM）. GNPs/CPE as a simple and sensitive electrode was used to study three important biological molecules： folic acid（FA）, uric acid（UA） and ascorbic acid（AA）. Square wave voltammetry（SWV） was used as an accurate technique for quantitative measurements. A good linear relation was observed between anodic peak current（ipa） and FA（5.2 × 10（-6）– 2.5 × 10（-5）M）, UA（1.2 × 10（-6）– 2.1 × 10（-5）M） and AA（1.2 × 10（-6）– 2.5 × 10（-5）M） concentrations in simultaneous determination of these molecules.
基金Project supported by the National Natural Science Foundation of China.
文摘Standard electrode potentials E° of Ag-AgC1 electrode in molality scale and acidity constants of glyeine pK_1° at constant molality of NaCl (1.0 mol·kg^(-1)) in 5 and 15 mass% glucose-water mixed solvents over a range of temperatures from 278.15 to 318.15 K were determined from precise emf measurements.The dependence of acidity constant on temperature is given as a function of the thermodynamic temperature T by an empirical equation, pK_1° =A_1(K/T)-A_2+A_3(T/K).The corresponding thermodynamic quantities of the first dissociation process of glycine were calculated and the effects of both tho solvent and the salt on them were also discussed.
文摘A carbon paste electrode（CPE） chemically modified with multiwall carbon nanotubes and ferrocene（FC） was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine（CA） and folic acid（FA）.This modified electrode showed very efficient electrocatalytic activity for the anodic oxidation of CA.The peak current of differential pulse voltammograms of CA and FA increased linearly with their concentration in the ranges of 0.7-200μmol/L CA and 5.0- 700μmol/L FA.The detection limits for CA and FA were 0.3μmol/L and 2.0μmoI/L,respectively.The diffusion coefficient（D） and transfer coefficient（α） of CA were also determined.These conditions are sufficient to allow determination of CA and FA both individually and simultaneously.
文摘In this study,Au nanoparticles/poly 5-[（2-hydroxynaphthalen-l-yl）diazenyl]isophthalic acid film modified glassy carbon electrode（AuNPs/poly（NDI）/GCE） has shown excellent electrocatalytic activity toward the oxidation of adrenaline（ADR）,paracetamol（PAC）,and tryptophan（Trp）.The bare glassy carbon electrode（GCE） fails to separate the oxidation peak potentials of these molecules,while the poly（NDI） film modified electrode can resolve them.Electrochemical impedance spectroscopy（EIS）indicates that the charge transfer resistance of the bare electrode decreases as 5-[（2-hydroxynaphthalen-l-yl）diazenyl]isophthalic acid is electropolymerized on the bare electrode.Furthermore,EIS exhibits enhancement of electron transfer kinetics between analytes and the electrode after electrodeposition of Au nanoparticles.Differential pulse voltammetry results show that the electrocatalytic current increases linearly in the ranges of 0.01-680.0 μmol L^-1 for ADR,0.05-498.0 μmol L^-1 for PAC,and 3.0-632.0 μmol L^-1 for Trp;with detection limits（S/N = 3） of 0.009 μmol L^-1,0.005 μmol L^-1,and 0.09 μmol L^-1 for ADR,PAC,and Trp,respectively.The proposed method has been successfully applied for simultaneous determination of ADR,PAC,and Trp in biological samples.
