Validation method for fire gas analysis — Part 2: Intralaboratory validation of quantification methods (ISO 12828-2:2016)
This document describes tools and techniques for use in validating the analysis of fire gases when ananalytical method is developed in a laboratory. It complements ISO 12828-1, which deals with limits ofquantification and detection.The tools and techniques described can be applied to the measurement of quantities, concentrations(molar and mass), volume fractions, and concentration or volume fraction versus time analyses. Fireeffluents are often a complex matrix of chemical species, strongly dependent on the materials involvedin the fire, but also dependent on fire scenario parameters (see ISO 19706). With such a wide varietyof conditions, the analytical techniques available will differ in terms of the influence of the matrixon the methods and on the concentration ranges which can be measured. The analytical techniquesavailable are likely to differ significantly in several respects, such as their sensitivity to the matrix andthe range of concentrations/ volume fractions which can be reliably measured. For these reasons, aunique reference analytical technique for every fire effluent of interest is, in practical terms, difficultor impossible to achieve. The tools in this document allow verification of the reliable measurementranges and conditions for the analysis of fire effluents, thereby enabling a comparison among variousanalytical techniques.Examples of existing International Standards where the information contained in this document canbe used are the analytical chemical methods in ISO 19701, ISO 19702, ISO 5660-1, and the chemicalmeasurements in the methods discussed in ISO/ TR 16312-2, ISO 16405, or their application to firetoxicity assessment using ISO 13571 and ISO 13344.NOTE 1 The variable “concentration” is used throughout this document, but it can be replaced in all placeswith “volume fraction” without altering the meaning. This does not apply to the Annexes.NOTE 2 Concentration can be calculated from volume fraction by multiplying by the density of the relevantgas at the relevant temperature and pressure.
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