Four kinds of high surface area activated carbon(HSAAC) were prepared from petroleum coke by KOH activation in this article. Modified glassy carbon electrodes with high surface area activated carbon(HSAAC/GCE)were prepared by dropping HSAAC on the substrate of glassy carbon electrode.Electrocatalysis of HSAAC/GCE to the electrochemical reaction of p-dihydroxybenzene was investigated by use of cyclic voltammetry and electrochemical impedance spectroscopy. The results show that the electrode process is controlled by diffusion. The HSAAC/GCE presents the high electrocatalytic activity to the redox reaction of p-dihydroxybenzene. Compared to the naked glass carbon electrode, the currents of the anodic and cathodic peak for HSAAC/GCE increased by 17.9 and 29.8 times, respectively, when the HSAAC/GCE was used. In the 0.1 mol/L HCl solution, the anodic peak current increases linearly with the concentration of p-dihydroxybenzene in the range of 0.01-7 mmol/L, and the linear equation can be expressed by Ipa(mA)=9E-06+5E-05×C(mmol/L) (R2=0.9967).p-dihydroxybenzene, o-dihydroxybenzene and m-dihydroxybenzene are three isomers of dihydroxybenzene. HSAAC/GCE showed electrocatalytic responses towards o-dihydroxybenzene and m-dihydroxybenzene as well as that toward p-dihydroxybenzene.In addition, the difference between the anodic potentiala on the cyclic voltammograms of p-dihydroxybenzene and o-dihydroxybenzene could be as wide as 0.100V on the HSAAC/GCE. Thus, the HSAAC/GCE can be applied to simultaneous determination of p-dihydroxybenzene,o-dihydroxybenzene and m-dihydroxybenzene. Moreover, the HSAAC/GCE could be readily prepared and is stable in the properties.In this work, four kinds of HSAAC were used to adsorb p-dihydroxybenzene, o-dihydroxybenzene and m-dihydroxybenzene. The results showed that the adsorption isotherms for the adsorption of p-dihydroxybenzene, o-dihydroxybenzene and m-dihydroxybenzene on the HSACCs were well described by Langmuir equation. A higher adsorption capacity of HSACCs lead to a stronger electrocatalysis of HSACC/GCE to the redox reaction of dihydroxybenzene.
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