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This work describes the electrochemical behaviour of ibuprofen on two types of multi-walled carbon nanotubes based composite electrodes,i.e.,multi-walled carbon nanotubes-epoxy(MWCNT) and silver-modified zeolite-multi-walled carbon nanotubes-epoxy(AgZMWCNT) composites electrodes.The composite electrodes were obtained using two-roll mill procedure.SEM images of surfaces of the composites revealed a homogeneous distribution of the composite components within the epoxy matrix.AgZMWCNT composite electrode exhibited the better electrical conductivity and larger electroactive surface area.The electrochemical determination of ibuprofen(IBP) was achieved using AgZMWCNT by cyclic voltammetry,differential-pulsed voltammetry,square-wave voltammetry and chronoamperometry.The IBP degradation occurred on both composite electrodes under controlled electrolysis at 1.2 and 1.75 V vs.Ag/AgCl,and IBP concentration was determined comparatively by differential-pulsed voltammetry,under optimized conditions using AgZMWCNT electrode and UV-Vis spectrophotometry methods to determine the IBP degradation performance for each electrode.AgZMWCNT electrode exhibited a dual character allowing a double application in IBP degradation process and its control.
This work describes the electrochemical behavior of ibuprofen on two types of multi-walled carbon nanotubes based composite electrodes, ie, multi-walled carbon nanotubes-epoxy (MWCNT) and silver-modified zeolite-multi-walled carbon nanotubes-epoxy electrodes. The composite electrodes were obtained using two-roll mill procedure. SEM images of surfaces of the composites revealed a homogeneous distribution of the composite components within the epoxy matrix. The determination of ibuprofen (IBP) was achieved using AgZMWCNT by cyclic voltammetry, differential-pulsed voltammetry, square-wave voltammetry and chronoamperometry. IBP-depleted on both composite electrodes under controlled electrolysis at 1.2 and 1.75 V vs. Ag / AgCl, and IBP concentration was determined comparatively by differential-pulsed voltammetry, under optimized conditions using AgZMWCNT electrode and UV-Vis spectrophotometry methods to determine the IBP degradation performance for each electrode.