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The investigation and development of a chemiluminescence based ethanol detection concept into a biosensor system is described. The biosensor uses alcohol oxidase to catalyze the reaction of short chain primary alcohols with elemental oxygen to produce hydrogen peroxide and the corresponding aldehyde. The reaction of hydrogen peroxide with an organic luminophore in the presence of a sufficient electric field results in emission of blue light with peak intensity at 425nm. The chemiluminescent light intensity is directly proportional to the alcohol concentration of the sample. The aqueous phase chemistry required for sensor operation is implemented using solid phase modules which adjust the pH of the influent stream, catalyze the oxidation of alcohol, provide the controlled addition of the luminophore to the flowing aqueous stream, and minimize the requirement for expendables. Precise control of the pH has proven essential for the long-term sustained release of the luminophore.

The initial development effort is described for an electrochemical hydrogen peroxide generator and pervaporation module capable of producing and delivering hydrogen peroxide to a contaminated waste water stream as an oxidant or to a pure water stream for use as a disinfectant. A three chambered cell is used to generate hydrogen peroxide by a combined electrodialysis and electrochemical process. Each chamber is separated from its neighbor by a membrane allowing selective production of peroxide anions and hydrogen ions under controlled pH conditions followed by migration to form hydrogen peroxide. Concentrations greater than 6,500mg/L have been produced in this manner. The effects of voltage, pH, membranes, electrode materials, and method of oxygen introduction are delineated. Hydrogen peroxide is then transferred to the end-use stream by pervaporation. The impact of pH, relative flow rates, and ionic strength of sink and source solutions on pervaporation rates is detailed.