Cyclic, differential-pulse, and square-wave voltammetric techniques were used to probe carbaryl (CB), carbofuran (CF), and malathion in Carmody buffers of pH 2–12. Oxidation of CF occurred at the three overpotentials 1.31 V, 1.44 V, and 1.69 V, and a broad reduction peak was observed at 1.10 V, referred against Ag|AgCl. Compared with the oxidation of CB at 1.35 V, these electrochemical differences allowed for simultaneous detection of both compounds. This non-enzymatic sensor demonstrated a linear calibration over a concentration range of 1–100 µM for CB (R=0.9834) and CF (R=0.9938). After exposure to 1 mM malathion, a reduction peak appears that is highly sensitive to pH, attributed to a complex carbon–oxygen adsorbate that is robust to aggressive cleaning methods and only removable by hydrogen plasma etching. This malathion modified surface may be advantageous in future applications such as pH sensing. The oxidised BDD demonstrated failsafe reproducibility, a linear response, and low detection limits at medically relevant concentrations.
References
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