EN 15550:2007

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Futtermittel - Bestimmung von Cadmium und Blei mittels Graphitrohrofen-Atomabsorptionsspektrometrie (GF-AAS) nach DruckaufschlussAliments des animaux - Détermination de la teneur en cadmium et en plomb par spectrométrie d'absorption atomique a four graphite (GF-AAS) apres digestion sous pressionAnimal feeding stuffs - Determination of cadmium and lead by graphite furnace atomic absorption spectrometry (GF-AAS) after pressure digestion65.120KrmilaAnimal feeding stuffsICS:Ta slovenski standard je istoveten z:EN 15550:2007SIST EN 15550:2008en,fr,de01-februar-2008SIST EN 15550:2008SLOVENSKI
STANDARD
EUROPEAN STANDARDNORME EUROPÉENNEEUROPÄISCHE NORMEN 15550October 2007ICS 65.120 English VersionAnimal feeding stuffs - Determination of cadmium and lead bygraphite furnace atomic absorption spectrometry (GF-AAS) afterpressure digestionAliments des animaux - Détermination de la teneur encadmium et en plomb par spectrométrie d'absorptionatomique à four graphite (GF-AAS) après digestion souspressionFuttermittel - Bestimmung von Cadmium und Blei mittelsGraphitrohrofen-Atomabsorptionsspektrometrie (GF-AAS)nach DruckaufschlussThis European Standard was approved by CEN on 26 August 2007.CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this EuropeanStandard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such nationalstandards may be obtained on application to the CEN Management Centre or to any CEN member.This European Standard exists in three official versions (English, French, German). A version in any other language made by translationunder the responsibility of a CEN member into its own language and notified to the CEN Management Centre has the same status as theofficial versions.CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland,France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMITÉ EUROPÉEN DE NORMALISATIONEUROPÄISCHES KOMITEE FÜR NORMUNGManagement Centre: rue de Stassart, 36
B-1050 Brussels© 2007 CENAll rights of exploitation in any form and by any means reservedworldwide for CEN national Members.Ref. No. EN 15550:2007: ESIST EN 15550:2008

Results of the interlaboratory tests.12 Annex B (informative)
Notes on the detection technique, interferences and quantification, pressure digestion.14 Bibliography.16
The limit of detection is numerically equal to three times the standard deviation of the mean of blank determinations (n ≥ 10, where n = number of measures) performed under reproducibility conditions. 3.2 limit of quantification (LOQ) lowest content of the analyte that can be measured with reasonable statistical certainty NOTE
If both trueness and precision are constant over a concentration range around the limit of detection, then the limit of quantification is numerically equal to ten times the standard deviation of the mean of blank determinations (n ≥ 10, were n = number of measures) performed under reproducibility conditions. 3.3 feed additives substances that comply with the definition of feed additives given in the Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition 3.4 animal feeding stuffs substances that comply with the definition of animal feeding stuffs given in the Regulation (EC) No 178/2002 SIST EN 15550:2008

The concentration of the elements is determined by graphite furnace atomic absorption spectrometry (GF-AAS) using external calibration.
The method detection limit for each element is dependent on the sample matrix as well as the instrument, the type of atomizer and the use of chemical modifiers. A typical sample volume of 10 µl to 20 µl is used. WARNING – Use of this European Standard can involve hazardous materials, operations and equipment. This standard does not purport to address all the safety problems associated with its use. It is the responsibility of the user of this European Standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. 5 Reagents 5.1 General Use only reagents of recognized analytical grade, and water conforming to grade 2 of EN ISO 3696. 5.2 Nitric Acid, concentrated, not less than 65 % (mass fraction), c(HNO3) = 14,4 mol/l, having a density of approximately ρ (HNO3) = 1,42 g/ml.
5.3 Hydrogen peroxide, mass fraction not less than 30 %. 5.4 Element stock solutions
Cd, Pb c = 1 000 mg/l The user should choose a suitable stock solution. Both single-element stock solutions and multi-element stock solutions with adequate specifications stating the acid used and the preparation technique are commercially available. It is advisable to use certified stock solutions. Stock solutions should not be used after expiration dates. Element stock solutions with concentrations different from 1 000 mg/l may also be used. 5.5 Calibration solutions
Prepare a range of standards including a blank calibration solution, which covers the linear range of the element to be determined by diluting the element stock solutions (5.4). Appropriate matrix matching of the calibration solutions shall be performed (see Annex B), e.g. adjust the acid concentration of the standards to the acid concentration of the samples. Dilute to volume with water.
5.6 Matrix modifier (e.g. Palladium nitrate/magnesium nitrate modifier) Pd(NO3)2 solution (Pd-nitrate solution) is commercially available (mass concentration 10 g/l). Dissolve 0,259 g of Mg(NO3)2 6H20 (Mg-nitrate solution) in 100 ml of water. Mix the Pd-nitrate solution with twice as much Mg-nitrate solution. 10 µl of the mixed solution is equal to 15 µg Pd and 10 µg Mg(NO3)2. It is advisable to use this solution for not longer than one week. SIST EN 15550:2008

6.1.1 Use laboratory grinders that are equipped so that samples cannot be contaminated. 6.1.2 Laboratory grinder capable of grinding to a particle size of less than or equal to 1 mm, e.g. a knife mill or equivalent. 6.1.3 Laboratory grinder capable of grinding to a particle size of less than or equal to 0,1 mm, e.g. a ball mill or equivalent. 6.1.4 Mortar with pestle, free of contamination. 6.2 Analytical balance, capable of weighing with an accuracy of 1 mg. 6.3 Pressure digestion apparatus, commercially available.
The apparatus shall be tested for safety pressure vessels made of acid-resistant materials and having holders for the sample of acid-resistant material with a low level of contamination. Apparatus are available that uses a high-pressure incinerator with or without ambient autoclave pressure.
Instead of polytetrafluoroethylene (PTFE) holders, it is better to use graduated quartz holders, perfluoro ethylene propylene (FEP) holders or perfluoro alkoxy (PFA) holders. Quartz is advisable to be used for decomposition temperatures above 230 °C. 6.4 Graphite furnace atomic absorption spectrometer, with background correction, e.g. Zeeman, supplied with auto sampler, an appropriate gas (5.7) supply and hollow cathode lamps or EDL-lamps for lead and cadmium. NOTE It is necessary to place an exhaust venting system over the furnace to remove any smoke and vapours that might be harmful. 6.5 Graphite tubes, pyrolytically coated and preferably with platforms. 6.6 Freeze drying equipment, capable of freeze-drying liquid animal feeding stuffs. 7 Sampling Sampling is not part of the method specified in this International Standard. A recommended sampling method is given in EN ISO 6497. It is important that the laboratory receives a sample that is truly representative and has not been damaged or changed during transport or storage. SIST EN 15550:2008

 Grinding must be done in conditions such that the substance is not appreciably heated.
 Operation is to be repeated as many times as is necessary and it must be effected as quickly as possible in order to prevent any gain or loss of constituents (water).
 Whole ground product is placed in a flask made of e.g. polypropylene, which can be stoppered and stored in such way to prevent any change in composition.
 Before any weighing is carried out for the analysis, the whole test sample must be thoroughly mixed for reasons of homogeneity.
8.2 Animal feeding stuffs which can be ground as such
Grind the laboratory sample (usually 500 g), using a grinder (6.1.2) or mortar (6.1.4), until a particle size of 1 mm or less has been reached. 8.3 Liquid animal feeding stuffs
8.3.1 General Liquid feeding stuffs shall be pre-dried according to the procedure described in 8.3.2 or freeze-dried according to the procedure described in 8.3.3. 8.3.2 Pre-drying Pre-dry the laboratory sample at 70 °C ± 5 °C during at least 16 h to reduce the moisture content. The mass of the sample before and after the pre-drying is to be determined using an analytical balance (6.2). Grind the pre-dried sample in accordance with 8.2.
8.3.3 Freeze-drying Freeze-dry the laboratory sample following the instructions of the freeze-drying equipment (6.6). The mass of the sample before and after the freeze-drying is to be determined using an analyt
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