ISO 1871
INTERNATIONAL STANDARD
Second edition 2009-09-01
Food and feed products — General guidelines for the determination of nitrogen by the Kjeldahl method Produits alimentaires et aliments des animaux — Lignes directrices générales pour le dosage de l'azote selon la méthode de Kjeldahl
Reference number ISO 1871:2009(E)
© ISO 2009
ISO 1871:2009(E)
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© ISO 2009 – All rights reserved
ISO 1871:2009(E)
Foreword
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ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2.
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The main task of technical committees is to prepare International Standards. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote.
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Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. ISO 1871 was prepared by Technical Committee ISO/TC 34, Food products.
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This second edition cancels and replaces the first edition (ISO 1871:1975), which has been technically revised.
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© ISO 2009 – All rights reserved
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ISO 1871:2009(E)
Introduction The analysis of products of animal or plant origin, such as those used in food and feed products, often includes determining their nitrogen content according to the Kjeldahl method.
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This method can be standardized in principle, as it is generally accepted that different apparatus or operating methods are equivalent if their results are similar. The purpose of this document is to describe the various stages of the method, the associated critical points and the minimum objectives to be achieved to ensure that the method is applied correctly.
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This document provides general guidelines; it is not intended to replace existing International Standards which are in use.
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© ISO 2009 – All rights reserved
INTERNATIONAL STANDARD
ISO 1871:2009(E)
Food and feed products — General guidelines for the determination of nitrogen by the Kjeldahl method
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WARNING — The use of this International Standard may involve hazardous materials, operations and equipment. This International Standard does not purport to address all the safety problems associated with its use. It is the responsibility of the user of this International Standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
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Scope
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NOTE
This measurement principle does not take into account the nitrogen from nitrates and nitrites.
Principle
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This International Standard provides general guidelines for the determination of nitrogen by the Kjeldahl method. It applies to food and feed products containing nitrogenous compounds that can be directly determined by the Kjeldahl method.
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Digestion of a test portion with concentrated sulfuric acid in the presence of catalysts to convert the organic nitrogen into ammonium sulfate. Excess sodium hydroxide is added to the cooled digest to release the ammonia. The released ammonia is distilled into an excess of boric acid solution and then titrated with a standard solution of sulfuric or hydrochloric acid. The nitrogen content is calculated from the quantity of ammonia produced.
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In the following text, the term “nitrogen” refers to organic nitrogen.
Reagents
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NOTE
Use only reagents of recognized analytical grade, unless otherwise specified, and distilled or demineralized water or water of equivalent purity.
3.2
Catalysts (see 5.2.1).
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3.1 Sulfuric acid, virtually free from nitrogenous compounds and of mass density ρ20 = 1,83 g/ml to 1,84 g/ml.
3.3 Boric acid solution (10 g/l to 40 g/l depending on the apparatus used). If using the colorimetric end-point titration, boric acid solution shall contain indicator (the pH or colour of this mixed solution shall be adjusted before use). 3.4 Standard hydrochloric acid (0,02 mol/l to 0,50 mol/l) or sulfuric acid solution (0,01 mol/l to 0,25 mol/l). The titre of the solution, ct, shall be known to at least within 0,001 mol/l. 3.5
Indicators, which should change colour between pH 4 and pH 5.
NOTE Various indicators are available. A methyl red and bromocresol green mixed indicator is most commonly used. Ready-to-use boric acid solutions containing mixed indicators are available.
© ISO 2009 – All rights reserved
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