
Vlákniny, papír a lepenka - Stanovení primárních aromatických aminů (PAA) ve vodném výluhu metodou LC-MS (Norma k přímému použití jako ČSN).
NORMA vydaná dňa 1.7.2019
    
        Označenie normy: ČSN EN 17163
                Rozlišovací znak:  500361
                
                Katalógové číslo:  507400
                
                
               
                Dátum vydania normy:  1.7.2019
        Počet strán: 20
Približná hmotnosť: 60 g (0.13 libier)
        Krajina:          Česká technická norma
        Kategória: Technické normy ČSN
        
                
              
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