1、BS ISO 2962:2010ICS 67.100.30NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDCheese and processedcheese products Determination of totalphosphorus content Molecular absorptionspectrometric methodThis British Standard was published under the authority of the Stand
2、ards Policy and Strategy Committee on 31 July2010 BSI 2010ISBN 978 0 580 70104 7Amendments/corrigenda issued since publicationDate CommentsBS ISO 2962:2010National forewordThis British Standard is the UK implementation of ISO 2962:2010. Itsupersedes BS 770-6:1984 which is withdrawn.The UK participat
3、ion in its preparation was entrusted to TechnicalCommittee AW/5, Chemical analysis of milk and milk products.A list of organizations represented on this committee can be obtained onrequest to its secretary.This publication does not purport to include all the necessary provisionsof a contract. Users
4、are responsible for its correct application. Compliance with a British Standard cannot confer immunityfrom legal obligations.BS ISO 2962:2010Reference numbersISO 2962:2010(E)IDF 33:2010(E)ISO and IDF 2010INTERNATIONAL STANDARD ISO2962IDF33Third edition2010-06-01Cheese and processed cheese products D
5、etermination of total phosphorus content Molecular absorption spectrometric method Fromages et fromages fondus Dtermination de la teneur en phosphore total Mthode par spectromtrie dabsorption molculaireBS ISO 2962:2010ISO 2962:2010(E) IDF 33:2010(E) PDF disclaimer This PDF file may contain embedded
6、typefaces. In accordance with Adobes licensing policy, this file may be printed or viewed but shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In downloading this file, parties accept therein the responsibility of not i
7、nfringing Adobes licensing policy. Neither the ISO Central Secretariat nor the IDF accepts any liability in this area. Adobe is a trademark of Adobe Systems Incorporated. Details of the software products used to create this PDF file can be found in the General Info relative to the file; the PDF-crea
8、tion parameters were optimized for printing. Every care has been taken to ensure that the file is suitable for use by ISO member bodies and IDF national committees. In the unlikely event that a problem relating to it is found, please inform the ISO Central Secretariat at the address given below. COP
9、YRIGHT PROTECTED DOCUMENT ISO and IDF 2010 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying and microfilm, without permission in writing from either ISO or IDF at t
10、he respective address below. ISO copyright office International Dairy Federation Case postale 56 CH-1211 Geneva 20 Diamant Building Boulevard Auguste Reyers 80 B-1030 Brussels Tel. + 41 22 749 01 11 Tel. + 32 2 733 98 88 Fax + 41 22 749 09 47 Fax + 32 2 733 04 13 E-mail copyrightiso.org E-mail infof
11、il-idf.org Web www.iso.org Web www.fil-idf.org Published in Switzerland ii ISO and IDF 2010 All rights reservedBS ISO 2962:2010ISO 2962:2010(E) IDF 33:2010(E) ISO and IDF 2010 All rights reserved iiiForeword ISO (the International Organization for Standardization) is a worldwide federation of nation
12、al 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. Internatio
13、nal 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 rule
14、s given in the ISO/IEC Directives, Part 2. 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 l
15、east 75 % of the member bodies casting a vote. 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 2962IDF 33 was prepared by Technical Committee ISO
16、/TC 34, Food products, Subcommittee SC 5, Milk and milk products, and the International Dairy Federation (IDF). It is being published jointly by ISO and IDF. This third edition of ISO 2962IDF 33 cancels and replaces the second edition (ISO 2962:1984), of which it constitutes a minor revision. BS ISO
17、 2962:2010ISO 2962:2010(E) IDF 33:2010(E) iv ISO and IDF 2010 All rights reservedForeword IDF (the International Dairy Federation) is a non-profit organization representing the dairy sector worldwide. IDF membership comprises National Committees in every member country as well as regional dairy asso
18、ciations having signed a formal agreement on cooperation with IDF. All members of IDF have the right to be represented on the IDF Standing Committees carrying out the technical work. IDF collaborates with ISO in the development of standard methods of analysis and sampling for milk and milk products.
19、 The main task of Standing Committees is to prepare International Standards. Draft International Standards adopted by the Standing Committees are circulated to the National Committees for endorsement prior to publication as an International Standard. Publication as an International Standard requires
20、 approval by at least 50% of IDF National Committees casting a vote. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. IDF shall not be held responsible for identifying any or all such patent rights. ISO 2962IDF 33 was prepared by t
21、he International Dairy Federation (IDF) and Technical Committee ISO/TC 34, Food products, Subcommittee SC 5, Milk and milk products. It is being published jointly by IDF and ISO. All work was carried out by the former Joint ISO-IDF Action Team on Minor compounds, now part of the Standing Committee o
22、n Analytical methods for composition. This edition of ISO 2962|IDF 33 cancels and replaces IDF 33C:1987, of which it constitutes a minor revision. BS ISO 2962:2010INTERNATIONAL STANDARD ISO 2962:2010(E)IDF 33:2010(E) ISO and IDF 2010 All rights reserved 1Cheese and processed cheese products Determin
23、ation of total phosphorus content Molecular absorption spectrometric method 1 Scope This International Standard specifies a molecular absorption spectrometric method for the determination of the total phosphorus content of cheese. The method is applicable to all kinds of cheese and to processed chee
24、se products. 2 Terms and definitions For the purposes of this document, the following terms and definitions apply. 2.1 total phosphorus content in cheese and processed cheese products mass fraction of substances determined by the method specified in this International Standard NOTE Total phosphorus
25、content is expressed as a percentage mass fraction. 3 Principle Cheese is digested by concentrated sulfuric acid and hydrogen peroxide. Molybdenum blue is formed by addition of a sodium molybdate-ascorbic acid solution. Molecular absorption of the blue colour formed is measured spectrometrically at
26、a wavelength of 820 nm. NOTE Dry ashing can be used, provided that the procedure gives comparable results to the wet digestion. 4 Reagents Unless otherwise stated, use only reagents of recognized analytical grade and distilled or demineralized water or water of equivalent purity, free from phosphoru
27、s compounds. 4.1 Concentrated sulfuric acid (H2SO4), 20= 1,84 g/ml. 4.2 Hydrogen peroxide, solution containing about 30 g of H2O2per 100 ml. 4.3 Molybdate-ascorbic acid solution. 4.3.1 Sodium molybdate solution. Dissolve 12,5 g of sodium molybdate dihydrate (Na2MoO42H2O) in a 5 mol/l sulfuric acid s
28、olution, make up to 500 ml with this sulfuric acid solution and mix. BS ISO 2962:2010ISO 2962:2010(E) IDF 33:2010(E) 2 ISO and IDF 2010 All rights reserved4.3.2 Ascorbic acid solution. Dissolve 10 g of ascorbic acid (C6H8O6) in water, make up to 200 ml, and mix. This solution cannot be stored and sh
29、all be prepared immediately before use. 4.3.3 Mixed solution. Immediately before use, mix 25 ml of sodium molybdate solution (4.3.1) with 10 ml of ascorbic acid solution (4.3.2), make up to 100 ml with water, and mix. 4.4 Phosphorus, standard solution corresponding to 100 g of phosphorus per millili
30、tre. Dry, for at least 48 h, about 1 g of potassium dihydrogenorthophosphate (KH2PO4) in a desiccator over an efficient desiccant, e.g. concentrated sulfuric acid. Dissolve 0,439 4 g of the previously dried phosphate in water, make up to 1 000 ml, and mix. 5 Apparatus IMPORTANT All glassware shall b
31、e thoroughly cleaned with a phosphorus-free detergent and rinsed with water. Usual laboratory equipment and in particular the following. 5.1 Analytical balance. 5.2 Device for grinding or grating cheese, capable of being easily cleaned. 5.3 Water bath. 5.4 Digestion flasks (Kjeldahl flasks or digest
32、ion tubes), capacity 25 ml. 5.5 Heating apparatus. 5.5.1 Micro gas burners or electric heaters, for heating Kjeldahl flasks. 5.5.2 Heating block, for heating digestion tubes. 5.6 Glass beads. 5.7 Measuring cylinders, capacities 5 ml and 25 ml, ISO 47885class A. 5.8 One-mark volumetric flasks, capaci
33、ties 50 ml and 100 ml, ISO 10424class B. 5.9 Pipettes, capacities 1 ml, 2 ml, 3 ml, 5 ml and 10 ml, ISO 6481class B or ISO 8353. 5.10 Spectrometer, suitable for measurements at a wavelength of 820 nm, equipped with cells of optical pathlength 10 mm. 6 Sampling Sampling is not part of the method spec
34、ified in this International Standard. A recommended sampling method is given in ISO 707|IDF 502. It is important that the laboratory receive a truly representative sample which has not been damaged or changed during transport or storage. BS ISO 2962:2010ISO 2962:2010(E) IDF 33:2010(E) ISO and IDF 20
35、10 All rights reserved 37 Preparation of test sample Remove the rind, smear or mouldy surface layer of cheese, in such a way as to provide a sample representative of the cheese as it is usually consumed. Grind or grate the sample using an appropriate device (5.2). Mix the ground or grated mass quick
36、ly and, if possible, grind or grate a second time and again mix thoroughly. If the sample cannot be ground or grated, mix it thoroughly by intensive stirring and kneading. Transfer the test sample to an airtight container to await analysis, which should be carried out as soon as possible after grind
37、ing or grating. If delay is unavoidable, take all precautions to ensure proper preservation of the sample and to prevent condensation of moisture on the inside surface of the container. Clean the device after grinding or grating the sample. 8 Procedure 8.1 Test portion Into a digestion flask (5.4),
38、weigh, to the nearest 1 mg, a test portion of 0,5 g to 1,0 g of the test sample. If the water content of the cheese is less than 50 % mass fraction, a test portion of approximately 0,5 g is sufficient. In the case of fresh cheese, a test portion of approximately 1,0 g can be taken. 8.2 Determination
39、 8.2.1 Add three glass beads and 4 ml of the concentrated sulfuric acid (4.1) in a digestion flask and heat under a well-ventilated fume hood. A Kjeldahl flask shall be placed in an inclined position. Control the height of the flame so as to limit the production of foam in the flask. Foaming into th
40、e neck of the flask is allowed but the foam shall not escape. Maintain the mixture at simmering point. Avoid local overheating and avoid heating the flask above the surface of the liquid contents. 8.2.2 As soon as the foaming stops, cool to room temperature. Carefully add a few drops of the hydrogen
41、 peroxide solution (4.2), reheat, and repeat this procedure until the contents have become clear and colourless. During heating, mix the contents from time to time by careful swirling. Avoid local overheating. 8.2.3 Rinse the neck of the flask with about 2 ml of water, and heat the contents again un
42、til the water has evaporated. Allow the liquid to boil for 30 min after colour disappearance in order to destroy traces of hydrogen peroxide. Avoid local overheating. 8.2.4 Cool to room temperature. Quantitatively transfer the liquid contents into a 100 ml one-mark volumetric flask (5.8). Make up to
43、 the mark with water and mix well. 8.2.5 Pipette (5.9) 1 ml of the solution into a 50 ml one-mark volumetric flask (5.8) and dilute with about 25 ml of water. Add 20 ml of the molybdate-ascorbic acid solution (4.3.3). Make up to the mark with water and mix well. 8.2.6 Heat the flask in a boiling wat
44、er bath (5.3) for 15 min. 8.2.7 Cool to room temperature in a cold water bath (5.3). Within 1 h, measure the absorbance of the solution against that of the blank test solution (see 8.4) at a wavelength of 820 nm. BS ISO 2962:2010ISO 2962:2010(E) IDF 33:2010(E) 4 ISO and IDF 2010 All rights reserved8
45、.3 Calibration curve 8.3.1 Pipette (5.9) 10 ml of the phosphorus standard solution (4.4) into a 100 ml one-mark volumetric flask (5.8). Make up to the mark with water and mix well. 8.3.2 Pipette into a series of five 50 ml one-mark volumetric flasks (5.8) 0 ml, 1 ml, 2 ml, 3 ml, and 5 ml, respective
46、ly, of the diluted standard solution (8.3.1), i.e. equivalent to 0 g, 10 g, 20 g, 30 g, and 50 g of elemental phosphorus, respectively. Dilute the contents of each flask to approximately 20 ml with water. 8.3.3 Add 20 ml of the molybdate-ascorbic acid solution (4.3.3) to the contents of each volumet
47、ric flask. Make up to the mark with water and mix well. Proceed as specified in 8.2.6. 8.3.4 Cool to room temperature in cold water. Within 1 h, measure the absorbance of each of the calibration solutions against water as reference at a wavelength of 820 nm. 8.3.5 Plot these absorbances against the
48、amounts of elemental phosphorus added. 8.4 Blank test Carry out a blank test by following the procedure specified in 8.2, but without a test portion. 9 Calculation The total phosphorus content, wP, expressed as a percentage by mass, is given by the equation 1P0100mwm= where m0is the mass, in grams,
49、of the test portion; m1is the mass, in micrograms, of phosphorus, read from the calibration curve (or calculated from the regression line obtained by the method of least squares). Report the result to two places of decimals. 10 Precision 10.1 Repeatability The difference between two single results obtained on identical test material by one analyst using the same apparatus within a short time interval will exceed 0,03 g of phosphorus per 100 g of product on average not more than once in 20 cases in the normal an
copyright@ 2008-2019 麦多课文库（www.mydoc123.com）网站版权所有
备案/许可证编号：苏ICP备17064731号-1