Provided are a total organic carbon measurement method and a total organic carbon measurement device capable of determining whether or not an acid has been added to a sample. An acid is introduced into a reaction unit in which the sample is placed from a reservoir in which the acid is reserved (step S103). The conductivity of the sample into which the acid has been introduced is measured (step S105). The introduction of the acid from the reservoir into the reaction unit is detected on the basis of a change in the conductivity of the sample (step S107).

Apparatus and methods for measuring the concentrations of organic and inorganic carbon, or of other materials in aqueous samples are described, having a reactor that is resistively heated by passing an electric current through the reactor.

A measuring apparatus for determining the total organic carbon of a sample in a liquid medium includes a reactor block made of a metallic, electrically conductive, and corrosion-resistant material, the reactor block including a housing wall for accommodating a light source, the housing wall including an inlet into and an outlet from the reactor block and a flow chamber in which digestion of the sample for determining the total organic carbon occurs, the flow chamber configured to accommodate the light source and to route the sample to be irradiated with light, wherein the measuring apparatus further includes at least one conductivity measurement device, wherein the reactor block is an external electrode of the conductivity measurement device. A method for determining the total organic carbon of the sample using the measuring apparatus is disclosed.

A method and system of providing ultrapure water for semiconductor fabrication operations is provided. The water is treated by utilizing a free radical scavenging system. The free radical scavenging system can utilize actinic radiation with a free radical precursor compound, such as ammonium persulfate. The ultrapure water may be further treated by utilizing ion exchange media and degasification apparatus. A control system can be utilized to regulate a continuously variable intensity of the actinic radiation.

Various implementations include a device for analyzing total organic carbon (TOC) within a fluid. The device includes a primary container, an input conduit, and an output conduit. The primary container is hollow and has a primary side wall and a primary end wall. The primary side wall has an inner surface defining a primary cavity and an outer surface opposite and spaced apart from the inner surface. The primary end wall includes a septum that is resiliently penetrable by an analyzer needle of a grab analysis port of a TOC analyzer. The input conduit has an input lumen. The input conduit extends through the primary container such that the input lumen is in fluid communication with the primary cavity. The output conduit has an output lumen.

A sample heating unit 30 has a space in which an oxidation catalyst is arranged, and heats a sample arranged in the space. A carrier gas introduction unit 40 introduces inert gas containing water vapor as carrier gas into the sample heating unit 30. A detection unit 35 detects carbon dioxide generated by steam reforming reaction of organic carbon in a sample in the sample heating unit 30.

A method for determining a carbon content of a sample in a TOC analyzer, includes the steps of: directing a carrier gas from an inlet through a high temperature furnace to an analysis unit; stopping the flow of the carrier gas through the high temperature furnace; injecting the sample into the high temperature furnace, which is used to vaporize and/or oxidize the sample at a high temperature to form water vapor and carbon dioxide gas; waiting until the sample injected into the high temperature furnace is vaporized; starting the flow of the carrier gas through the high temperature furnace and thereby transporting the carbon dioxide gas produced during vaporization and/or oxidation of the sample to an analysis unit; and determining the carbon content of the sample by means of the analysis unit on the basis of the carbon dioxide gas produced during the oxidation of the sample.

An analytical device for automated determining of a measured variable of a liquid sample, includes: a base module; a replaceable cassette connectable with the base module and having at least one liquid container connectable via a fluid line with a measuring cell and containing a reagent to be added to the liquid sample for forming a measured liquid; and a measuring transducer for registering measured values correlated with the measured variable for the measured liquid accommodated in the measuring cell. The cassette has, associated with the at least one liquid container, a fluid coupling apparatus having a primary component and a secondary component and serving for producing a connection of the fluid line with the liquid container.

Disclosed is an analysis system for analyzing water and wastewater, comprising an analysis device that includes a device housing which accommodates device components and which has an inlet on a housing surface, said inlet being designed as an injection port through which a substance to be analyzed can be introduced into a device component when the device housing is closed, and comprising a syringe that includes an injection needle outlet, the surface normal of which is congruent with the longitudinal axis; and/or the syringe includes an automatic ejection element for ejecting a predetermined amount of substance within a predetermined injection period.

In one embodiment, a cavity-enhanced absorption spectroscopy system includes a cavity-enhanced absorbance cell in which a liquid sample can be provided for purposes of evaluation, the absorbance cell having diffusely reflective inner surfaces, a light source configured to emit light into the liquid sample within the absorbance cell, and a light detector configured to capture the light after it has passed through the liquid sample.