Electrophoresis-chemiluminescence detection of phenols catalyzed by hemin

Based on the catalytic activity of hemin, an efficient biocatalyst, an indirect capillary electrophoresis-chemiluminescence (CE-CL) detection method for phenols using a hemin-luminol-hydrogen peroxide system was developed. Through a series of static injection experiments, hemin was found to perform best in a neutral solution rather than an acidic or alkalinemedium. Although halide ions such as Br^- and F^- could further enhance the CL signal catalyzed by hemin, it is difficult to apply these conditions to this CE-CL detection systembecause of the self-polymerization of hemin, as it hinders the CE process. The addition of concentrated ammonium hydroxide to an aqueous/dimethyl sulfoxide solution of hemin-luminol afforded a stable CE-CL baseline. The indirect CE-CL detection of five phenols using this method gave the following limits of detections: 4.8 × 10^-8 mol/L (o-sec-butylphenol), 4.9 × 10^-8 mol/L (o-cresol), 5.4 × 10^-8 mol/L (m-cresol), 5.3 × 10^-8 mol/L (2,4-dichlorophenol) and 7.1 × 10^-8 mol/L (phenol).