作者: Mohammad Mazloum-Ardakani , Nooshin Rajabzadeh , Afsaneh Dehghani Firouzabadi , Ali Benvidi , Mohammad Abdollahi-Alibeik
DOI: 10.1039/C4AY00164H
关键词: Carbon paste electrode 、 Chemically modified electrode 、 Electrochemical gas sensor 、 Electrode 、 Analytical chemistry 、 Electrochemistry 、 Differential pulse voltammetry 、 Chemistry 、 Nuclear chemistry 、 Chronoamperometry 、 Hydroquinone
摘要: A nanostructure electrochemical sensor with a carbon paste electrode has been used to study the electrocatalytic oxidation of isoproterenol (IP) in presence uric acid, folic acid and tryptophan. In this work nanoparticles (CNPs) 7-(3,4-dihydroxyphenyl)-10,10-dimethyl-9,10,11,12-tetrahydrobenzo[c]acridin-9 (7H)-one (DDTA) were for investigation behaviour IP. An apparent charge transfer rate constant ks = 1.99 s−1, coefficient α 0.51, electron between modifier calculated. optimum pH (pH 9.0), IP at modified occurs potential about 298 mV less positive than unmodified electrode. The catalytic (k 134.28 M−1 s−1) diffusion (D 3.7 × 10−5 cm2 calculated by chronoamperometry. Differential pulse voltammetry (DPV) exhibited two linear dynamic ranges 0.25 20.0 μM 2000.0 There was decrease sensitivity second segment due kinetic limitations. Also, determine (UA), (FA) tryptophan (TRY) differential voltammetry. Simultaneous determination these four compounds performed on proposed first time. This from an ampoule sample. detection limit as 0.075 μM.