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Homepage>BS Standards>85 PAPER TECHNOLOGY>85.060 Paper and board>BS EN 17163:2019 Pulp, paper and board. Determination of primary aromatic amines (PAA) in a water extract by a LC-MS method
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BS EN 17163:2019 Pulp, paper and board. Determination of primary aromatic amines (PAA) in a water extract by a LC-MS method

BS EN 17163:2019

Pulp, paper and board. Determination of primary aromatic amines (PAA) in a water extract by a LC-MS method

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Standard number:BS EN 17163:2019
Pages:20
Released:2019-02-20
ISBN:978 0 580 96918 8
Status:Standard
DESCRIPTION

BS EN 17163:2019


This standard BS EN 17163:2019 Pulp, paper and board. Determination of primary aromatic amines (PAA) in a water extract by a LC-MS method is classified in these ICS categories:
  • 85.060 Paper and board

This document describes two representative methods for the determination of the extractable amount of specific primary aromatic amines (PAA) in a water extract of paper, board and pulp samples by means of HPLC with MS/MS detection which basically differ concerning the choice of the mobile and stationary phases. Deviating from this standard further methods may be applicable if it can be shown that comparable results can be achieved. A validation should be carried out by each laboratory.

It is applicable for the determination of the 22 primary aromatic amines (PAA) mentioned in the annex of Directive 2002/61/EC of 19th July 2002 amending Council Directive 76/769/EEC relating to restrictions on the market and use of certain dangerous substances and preparations (azocolourants) which are classified as carcinogenic categories 1A and 1B according to the CLP regulation and aniline.

The method described by this standard should be also applicable for the determination of further primary aromatic amines (PAA). A validation for every further analyte has to be done by the laboratory using this method.

The extractable amount of a primary aromatic amine (PAA) is expressed in mg PAA per litre water extract. This method is suitable for the determination of PAA with a working range of about 0,001 mg/l – 0,020 mg/l water extract.

Deviating from this standard further methods may be applicable if it can be shown that comparable results can be achieved. A validation should be carried out by each laboratory.