NF EN ISO 27108
Water quality - Determination of selected plant treatment agents and biocide products - Method using solid-phase microextraction (SPME) followed by gas chromatography-mass spectrometry (GC-MS)
ISO 27108:2010 specifies a method for the determination of the dissolved amount of selected plant treatment agents and biocide products in drinking water, ground water and surface water by solid‑phase microextraction (SPME) followed by gas chromatography-mass spectrometry (GC‑MS). The limit of determination depends on the matrix, on the specific compound to be analysed and on the sensitivity of the mass spectrometer. For most plant treatment agents and biocides to which ISO 27108:2010 applies, it is at least 0,05 µg/l. Validation data related to a concentration range between 0,05 µg/l and 0,3 µg/l have been demonstrated in an interlaboratory trial.This method may be applicable to other compounds not explicitly covered by ISO 27108:2010 or to other types of water. However, it is necessary to verify the applicability of this method for these special cases.
ISO 27108:2010 specifies a method for the determination of the dissolved amount of selected plant treatment agents and biocide products in drinking water, ground water and surface water by solid‑phase microextraction (SPME) followed by gas chromatography-mass spectrometry (GC‑MS). The limit of determination depends on the matrix, on the specific compound to be analysed and on the sensitivity of the mass spectrometer. For most plant treatment agents and biocides to which ISO 27108:2010 applies, it is at least 0,05 µg/l. Validation data related to a concentration range between 0,05 µg/l and 0,3 µg/l have been demonstrated in an interlaboratory trial.
This method may be applicable to other compounds not explicitly covered by ISO 27108:2010 or to other types of water. However, it is necessary to verify the applicability of this method for these special cases.
- Avant-proposiv
- Introductionv
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1 Domaine d'application1
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2 Références normatives1
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3 Principe1
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4 Interférences2
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4.1 Interférences lors de l'échantillonnage2
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4.2 Interférences lors du mode opératoire d'extraction2
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4.3 Interférences lors du mode opératoire de chromatographie en phase gazeuse et spectrométrie de masse3
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5 Réactifs4
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6 Appareillage6
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7 Échantillonnage et prétraitement de l'échantillon7
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8 Mode opératoire7
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8.1 Préparation des échantillons et extraction7
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8.2 Chromatographe en phase gazeuse8
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8.3 Identification des composés individuels par CG-SM8
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8.4 Mesurage des valeurs à blanc9
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9 Étalonnage9
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9.1 Exigences générales9
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9.2 Étalonnage avec un étalon interne couvrant le mode opératoire total10
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10 Calcul11
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11 Expression des résultats12
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12 Rapport d'essai12
- Annexe A (informative) Exemples de chromatogrammes en phase gazeuse pour les composés énumérés dans le Tableau 113
- Annexe B (informative) Spectres de masse des composés du Tableau 1 (balayage complet, impact électronique, 70 eV)23
- Annexe C (informative) Données de fidélité36
- Annexe D (informative) Informations générales sur la micro-extraction en phase solide (MEPS)38
- Bibliographie39
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