{"id":462720,"date":"2024-10-20T10:23:53","date_gmt":"2024-10-20T10:23:53","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-178922024\/"},"modified":"2024-10-26T19:17:05","modified_gmt":"2024-10-26T19:17:05","slug":"bs-en-178922024","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-178922024\/","title":{"rendered":"BS EN 17892:2024"},"content":{"rendered":"
This document specifies a method for the determination of the dissolved fraction of selected perfluoroalkyl and polyfluoroalkyl substances (PFAS) in non-filtrated drinking water using liquid chromatography-tandem mass spectrometry (LC-MS\/MS). The applicability of the method to other types of water like fresh waters (e.g. ground water, surface water) or treated wastewater can be validated separately for each individual case. For each target compound both, eventually occurring branched isomers and the respective non-branched isomer, are quantified together. The selected set of substances determined by this method is representative for a wide variety of PFAS. This method has been validated for the analytes specified in Table 1. The list given in this table can be modified depending on the purpose and focus of the method. The lower application range of this method can vary depending on the sensitivity of the equipment used and the matrix of the samples. For many substances to which this document applies a limit of quantification (LOQ) of 1 ng\/l can be achieved. Using high volume direct injection as described in part A or SPE as described in part B of the method allows lower LOQs. Analytical limitations can occur with short-chain PFAS or PFAS with more than ten carbon atoms in the carbon chain. Actual LOQs can depend on the blank values realized by individual laboratories as well. NOTE This document enables the analysis of those 20 PFAS which are listed in point 3 of Part B of Annex III of the EU Drinking Water Directive, EU 2020\/2184 [4], for the surveillance of the parametric limit value of 0,10 \u00b5g\/l for the sum of PFAS. Furthermore, alternatives and substitutes for these PFAS substances can be analysed using this document as well. Table 1 – Analytes for which a determination was validated in accordance with this method<\/p>\n
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2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | 1 Scope <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 4 Principle 5 Interferences 5.1 Sampling 5.2 Background contamination <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 5.3 Interferences encountered during liquid chromatography and mass spectrometry 6 Reagents <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 7 Apparatus <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 8 Sampling 9 Procedure 9.1 Part A: Method using direct injection 9.1.1 General 9.1.2 Sampling 9.1.3 Sample preparation <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 9.2 Part B: Method using SPE 9.2.1 General 9.2.2 Sampling 9.2.3 Sample preparation <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 9.2.4 Extraction <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 9.3 LC MS\/MS operating conditions <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 9.4 Blank determination 9.4.1 General 9.4.2 Method using direct injection 9.4.3 Method using SPE 9.5 Identification <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 9.6 Calibration 9.6.1 General requirements <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 9.6.2 Calibration using an external standard <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 9.6.3 Calibration using an internal standard <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 9.6.4 Calibration check 10 Calculation 10.1 Use of a calibration curve to determine concentration 10.2 Calculation of concentration using calibration with external standards <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | 10.3 Calculation of concentration using calibration with internal standards 10.4 Treatment of results outside the calibration range 10.5 Quantification of branched isomers <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | 11 Determination of analyte recovery 11.1 Recovery <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | 11.2 Recovery of internal standards 12 Expression of results 13 Test report <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | Annex A (informative)Performance data <\/td>\n<\/tr>\n | ||||||
37<\/td>\n | Annex B (informative)Instrumental conditions and chromatograms <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Water quality. Determination of selected per- and polyfluoroalkyl substances in drinking water. Method using liquid chromatography\/tandem-mass spectrometry (LC-MS\/MS)<\/b><\/p>\n |