Methods, articles of manufacture, and kits for calibrating fluid delivery systems are provided. A fluid delivery system connected to N input streams, where N is an integer greater than or equal to 2, mixes together fluid from the N input streams to form an output stream. The methods involve obtaining N test solutions, each containing a dye, providing optical absorbances of the test solutions at appropriate wavelengths, injecting the test solutions into the input streams, mixing the test solutions, and measuring the absorbance of the output stream at the same wavelengths. The methods also involve comparing the absorbances of the test solutions with the absorbances of the output stream, which can include calculating ratios and comparing the ratios with target values. The methods can further involve adjusting operation of the fluid delivery system based upon the absorbances. In some embodiments, the dyes have largely non-overlapping absorbance spectra.

A method and a corresponding device for calibrating a gas detection device with a measuring chamber for generating a gas chromatogram. A sequence of at least two consecutive partial injections separated by a pause is carried out, each comprising a predetermined amount of a sample-gas mixture to be injected into the measuring chamber, and the gas detection device generates a measurement signal by means of gas chromatography. The measurement signal correlates with the presence and/or concentration of a component of the sample-gas mixture. Due to the different partial injections, a plurality of measurement signals can be obtained, which means that depending on these measurement signals the necessary information for a calibration can be obtained automatically even if the transfer function of the detector unit is non-linear. In this way, a rapid and automated calibration can be achieved, which means a double advantage for the user.

A sample measurement device includes a measurement unit (1) configured to measure a sample, and a controller (2) configured to analyze a measurement result of the measurement unit. The controller (2) is configured to estimate and acquire a measurement result under another measurement condition using a model formula based on measurement results under a plurality of measurement conditions with different measurement parameter conditions, and estimate a distribution of a measurement quality indicator with respect to a measurement parameter based on the estimated measurement result.

Described are techniques for performing automated maintenance evaluations on a gas chromatograph (GC) or a gas chromatograph-mass spectrometer (GC-MS). Systems and methods are described for directing an injector of a GC or GC-MS instrument system to autonomously inject a diagnostic material sample into a material analysis chamber and initiate a scientific analysis to formulate a set of results. The systems and methods further include the instrument system analyzing the set of results generating one or more output reports.

Presented are improved and more sensitive methods for measuring levels of phytoestrogens in a biological sample, and specifically in a human urine sample, employing a High Pressure Liquid Chromatography method, coupled with a photodiode array analysis detection system. Calibration curve preparation for each of a panel of phytoestrogen analytes, including daidzein, equol and genistein, are provided employing techniques that demonstrate greater accuracy and sensitivity of sample level measurement. Clinically applicable techniques suitable for large population scale screening, diet and gut microflora characterization and disease analysis and correlation in human populations, such as in at risk breast cancer populations, through monitoring of phytoestrogen levels, is disclosed.

A method of operating a chromatography column is described. This method involves collecting column outlet signal and accumulated flow parameters at two or more intervals of at least one mobile phase transition front during operation of the chromatography column comprising column packing. A model gamma cumulative distribution curve is calculated based on the collected column outlet signal and accumulated flow parameters for the at least one mobile phase transition front. A height equivalent theoretical plate (HETP) value is calculated for the at least one mobile phase transition front using parameters of the model gamma cumulative distribution curve and the quality of the chromatography column packing is assessed based on the calculated HETP value.

An analysis method includes analyzing a reference sample that contains a predetermined amount of a predetermined component by an analysis device using a chromatograph and obtaining a reference detection value which is a detection value of the predetermined amount of the predetermined component detected by the analysis device, calculating a judgment reference value which is a criterion for judging whether a concentration of a detection subject component in a measurement subject sample is equal to or larger than a reference concentration or equal to or smaller than the reference concentration based on the reference detection value, and analyzing the measurement subject sample by the analysis device and judging that the detection subject component has been detected in a case where a detection value exceeding the judgment reference value is detected in a peak detection time zone corresponding to the detection subject component.

Apparatus for monitoring the quality of gas in a process stream at a subsea location comprises: a container for permanent installation at the location; one or more devices for analysing gas quality, said devices being located in the container; and means for supplying a sample of gas from the process stream to the said one or more devices; wherein the pressure within the container is maintained at or near to atmospheric pressure. The invention also extends to a method of monitoring the quality of gas in a process stream at a subsea location.

Provided is a method for measuring the concentration of aliphatic hydroxy oxime and neodecanoic acid using gas chromatography. The method includes the steps of: (a) removing, from a reference material containing an extractant and a diluent, the diluent using a silica column; (b) generating a calibration curve by calculating each peak area of aliphatic hydroxy oxime and neodecanoic acid, which are extractants, by peak integration of gas chromatograms; and (c) calculating the peak area of the organic solvent used in DSX process through the steps (a) and (b) and comparing the peak area with the calibration curve of the step (b) to measure the concentration of aliphatic hydroxy oxime and neodecanoic acid.

A monitoring analysis device includes an acquirer that sequentially acquires reaction products produced by a reactor, an analyzer that sequentially analyzes the reaction products acquired by the acquirer, a pre-processor that performs a pre-process to be performed before an analysis of the reaction products by the analyzer, and a controller that controls the pre-processor such that the pre-process for a second analysis to be performed subsequently to a first analysis is performed during the first analysis by the analyzer.