Abstract: An improved measurement cell and circuit for measuring the electrical characteristics of a liquid sample during exposure to radiation includes a glass cell formed of a main tube extending generally parallel to an elongated lamp emitting the radiation, and a pair of electrodes disposed axially within the sample tube. In the preferred embodiment, the ends of the cell are formed of glass twinbore tubing fused to the glass main tube, the bores retaining ends of the electrodes. Inlet and outlet tubes and a temperature sensing well may also be fused to the main tube. In an implementation for measurement of TOC in water by oxidation to CO.sub.2, the source comprises a low pressure mercury vapor lamp, and the electrodes are formed of solid Ti with catalytic TiO.sub.2 surfaces.

Abstract: An apparatus for removal of organic materials from water includes a reactor for photocatalytic oxidation and/or ionization of organics in the water stream and an ion exchange column for removal of CO.sub.2, dissolved acids, and ionized organics formed in the reactor from the water stream. The reactor includes an elongated flow chamber having an inlet at one end and an outlet at the opposite end. A photocatalytic material is provided as a surface layer on a number of solid members in the chamber, typically a number of rods extending generally parallel to the axis of the flow chamber. The catalyst may be TiO.sub.2 formed by oxidizing the surface of Ti rods. An elongated UV lamp fitting within a tubular quartz window extends along the axis of the reaction chamber. An external circuit connects the electrodes and the water, such that a current flows in the water in the reaction chamber. A potential of up to 600 VDC may be applied between the solid electrodes and water in the chamber.

Abstract: Apparatus and methods for measurement of total organic carbon content of water, particularly of low relative organic content, are described, featuring a single sample cell for exposure of a static sample to ultraviolet radiation and comprising electrodes for measuring the conductivity of the water. The conductivity is monitored as a function of time and the second time derivative of the conductivity signal is monitored to indicate when the oxidation reaction has been completed. Compensation for the contribution to conductivity of the water sample made by the instrument is achieved by subtracting a quantity proportional to the first time derivative of the conductivity at a time when the second time derivative reaches zero, indicating that the oxidation reaction is complete, from the change in the total conductivity measurement, the remainder being equal to the contribution to conductivity made by oxidation of the organic content of the water.

Abstract: The production of acid and base is effected by the electrolysis of a metal halide salt solution across an ion-exchange membrane. The base is removed directly from the cathode and the hydrogen and halogen gases produced at the electrodes are reacted in a catalytic column to form the acid. This gas is absorbed by water to form an aqueous hydrogen halide acid solution. Such a system can be operated automatically and on a small scale.