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Full-Text Articles in Chemistry

Electrochemical Behavior And Determination Of Luteolin At A Glassy Carbon Electrode, Ai-Lin Liu, Shao-Bo Zhang, Xiao-Sha Wu, Li-Ping Li, Yang-Yuan Cao, Li-Ying Huang, Xin-Hua Lin Nov 2007

Electrochemical Behavior And Determination Of Luteolin At A Glassy Carbon Electrode, Ai-Lin Liu, Shao-Bo Zhang, Xiao-Sha Wu, Li-Ping Li, Yang-Yuan Cao, Li-Ying Huang, Xin-Hua Lin

Journal of Electrochemistry

The electrochemical behavior of luteolin was studied by voltammetry at a glassy carbon electrode in phosphate buffer solution.The results exhibited that the well-defined redox peak of luteolin is observed and the electrode process is adsorption-controlled.The charge transfer coefficient(α) was calculated as 0.66 in phosphate buffer solution(pH 4.0).The relationships between oxidation peak current and the concentration of luteolin are linear in the range of 1.0×10-8 ~ 5.0×10-6 mol·L-1 by differential pulse voltammetric method.The detection limit had been estimated as 1.0×10-8 molL-1.This method can be used for the determination of luteolin with satisfactory results.


Mwnts Modified Gc Electrode For Hydrogen Peroxide Determination, Hong-Juan Wang, Chun-Mei Zhou, Hao Yu, Feng Peng, Jin-Kun Fang Feb 2007

Mwnts Modified Gc Electrode For Hydrogen Peroxide Determination, Hong-Juan Wang, Chun-Mei Zhou, Hao Yu, Feng Peng, Jin-Kun Fang

Journal of Electrochemistry

A MWNTs modified GC electrode was constructed successfully to be used to detect hydrogen peroxide.Two methods of maximum anodic current of cyclic voltommogram and chronoamperometry were adopted to measure the concentration of hydrogen peroxide.The results show that the MWCNTs can enlarge the effective surface area of GC electrode and can enormously enhance the electron transfer.The sensitivity and correlation coefficient for hydrogen peroxide detection are 2.84 μA/mmol·L-1,0.997 and 1.5 μA/mmol·L-1,0.971 for cyclic voltammetry and chronoamperometry,respectively.The procedure of the two methods to detect hydrogen peroxide is simple,and the results obtained are satisfied.


Use Of Factor Analysis In Multi‐Electron Spectroelectrochemistry, Michael D. Ryan, Robert L. Keesey Jan 2007

Use Of Factor Analysis In Multi‐Electron Spectroelectrochemistry, Michael D. Ryan, Robert L. Keesey

Chemistry Faculty Research and Publications

Spectroelectrochemistry and voltammetry contain both unique and complementary information. For multielectron transfers, information on each electron exchange is only directly accessible in the voltammetric data if the potentials are well separated so that two distinct waves can be observed. If the E°’s are close together, the voltammetric data will contain the sum of the two exchanges which can only be deconvoluted by modeling the system and solving the appropriate equations. On the other hand, the spectroscopic data contains direct information on each electron exchange even when the E°’s are close together. Unfortunately, this information cannot be readily extracted if the …


Voltammetric And Spectroscopic Studies Of Vanadium(V)-- Nicotinamide Interactions At Physiological Ph, Semi̇ha Çakir, Ender Bi̇çer Jan 2007

Voltammetric And Spectroscopic Studies Of Vanadium(V)-- Nicotinamide Interactions At Physiological Ph, Semi̇ha Çakir, Ender Bi̇çer

Turkish Journal of Chemistry

The interaction of nicotinamide (NA) with NH_4VO_3 at the physiological pH (pH 7.4) was studied by voltammetry and UV-Vis spectroscopy. The reduction of V(V) ions complexed with NA in phosphate buffer (pH 7.4) was observed as a well-defined reversible reduction peak at --0.35 V. The stoichiometric (metal:ligand) ratio of the complex of V(V) with NA was determined as 1:2 by the mole ratio method.