BS ISO 6561-1-2005 en_9732 Fruits vegetables and derived products - Determination of cadmium content - Method using graphite furnace atomic absorption spectrometry《水果、蔬菜及其制品.镉含量测定.石墨炉原子吸收光谱测定法》.pdf

《BS ISO 6561-1-2005 en_9732 Fruits vegetables and derived products - Determination of cadmium content - Method using graphite furnace atomic absorption spectrometry《水果、蔬菜及其制品.镉含量测定.石墨炉原子吸收光谱测定法》.pdf》由会员分享，可在线阅读，更多相关《BS ISO 6561-1-2005 en_9732 Fruits vegetables and derived products - Determination of cadmium content - Method using graphite furnace atomic absorption spectrometry《水果、蔬菜及其制品.镉含量测定.石墨炉原子吸收光谱测定法》.pdf（12页珍藏版）》请在麦多课文档分享上搜索。

1、BRITISH STANDARD BS ISO 6561-1:2005 Fruits, vegetables and derived products Determination of cadmium content Part 1: Method using graphite furnace atomic absorption spectrometry ICS 67.080.01 BS ISO 6561-1:2005 This British Standard was published under the authority of the Standards Policy and Strat

2、egy Committee on 24 January 2005 BSI 24 January 2005 ISBN 0 580 45353 7 National foreword This British Standard reproduces verbatim ISO6561-1:2005 and implements it as the UK national standard. Any enquiries on this text should be forwarded to Head of International Content, Standards Development, BS

3、I, 389 Chiswick High Road, London W4 4AL who will present to the responsible international/European committee any such enquiries on the interpretation, or proposals for change, and keep UK interests informed. Cross-references The British Standards which implement international publications referred

4、to in this document may be found in the BSI Catalogue under the section entitled “International Standards Correspondence Index”, or by using the “Search” facility of the BSI Electronic Catalogue or of British Standards Online. This publication does not purport to include all the necessary provisions

5、 of a contract. Users are responsible for its correct application. Compliance with a British Standard does not of itself confer immunity from legal obligations. Summary of pages This document comprises a front cover, an inside front cover, the ISO title page, pages ii and iii, a blank page, pages 1

6、to 5 and a back cover. The BSI copyright notice displayed in this document indicates when the document was last issued. Amendments issued since publication Amd. No. Date Comments Reference number ISO 6561-1:2005(E)INTERNATIONAL STANDARD ISO 6561-1 First edition 2005-02-01 Fruits, vegetables and deri

7、ved products Determination of cadmium content Part 1: Method using graphite furnace atomic absorption spectrometry Fruits, lgumes et produits drivs Dtermination de la teneur en cadmium Partie 1: Mthode par spectromtrie dabsorption atomique avec four en graphite BSISO65611:2005DPlcsid Fremia ihTs PDF

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11、d 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 technica

12、l 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 ele

13、ctrotechnical standardization. International Standards are drafted in accordance with the rules 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 th

14、e member bodies for voting. Publication as an International Standard requires approval by at least 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 ide

15、ntifying any or all such patent rights. ISO 6561-1 was prepared by Technical Committee ISO/TC 34, Food products, Subcommittee SC 3, Fruit and vegetable products. This first edition of ISO 6561-1, together with ISO 6561-2:2004, cancels and replaces ISO 6561:1983, which has been technically revised. I

16、SO 6561 consists of the following parts, under the general title Fruits, vegetables and derived products Determination of cadmium content: Part 1: Method using graphite furnace atomic absorption spectrometry Part 2: Method using flame atomic absorption spectrometry BSISO65611:2005 1Fruits, vegetable

17、s and derived products Determination of cadmium content Part 1: Method using graphite furnace atomic absorption spectrometry 1 Scope This part of ISO 6561 specifies a graphite furnace atomic absorption spectrometric method for the determination of the cadmium content of fruits, vegetables and derive

18、d products. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. ISO 5515:1979,

19、 Fruits, vegetables and derived products Decomposition of organic matter prior to analysis Wet method 3 Principle Organic matter is decomposed by a wet method and the dissolved cadmium is determined by graphite furnace atomic absorption spectrometry. 4 Reagents Use only reagents of recognized analyt

20、ical grade, and which, with the exception of the cadmium sulfate hydrate (4.8) and the cadmium standard solutions (4.9 and 4.10), shall be free from cadmium. Use only water which has been double-distilled in borosilicate glass apparatus, or water of at least equivalent purity. 4.1 Sulfuric acid, con

21、centrated, 20= 1,84 g/ml. 4.2 Nitric acid, 20= 1,38 g/ml. 4.3 Perchloric acid, 20= 1,67 g/ml. 4.4 Sulfuric acid, dilute, 10 % (volume fraction). 4.5 EDTA (ethylenediaminetetraacetic acid, disodium salt), 0,20 mol/l solution. 4.6 Buffer solution, pH 9. Dissolve 5,4 g of ammonium chloride in water and

22、 transfer to a 100 ml one-mark volumetric flask. Add 35 ml of 25 % (volume fraction) ammonia solution and make up to the mark with water. BSISO65611:20052 4.7 Eriochrome black T, 1 % (mass fraction) mixture with sodium chloride. 4.8 Cadmium sulfate hydrate (3CdSO 4 8H 2 O). The titre of the cadmium

23、sulfate shall be verified as follows. Weigh exactly 102,6 mg of cadmium sulfate hydrate, transfer quantitatively to a conical flask with water and shake until dissolved. Add 5 ml of the buffer solution (4.6) and about 20 mg of the eriochrome black T mixture (4.7). Titrate with the EDTA solution (4.5

24、) until the end point is reached as indicated by a change of colour to blue. The volume of EDTA used shall be 20 ml. If the volume differs slightly, correct the mass of cadmium sulfate used to prepare the standard cadmium solution (4.9) accordingly. 4.9 Cadmium standard solution, corresponding to 1,

25、0 mg of cadmium per mililitre. 4.10 Cadmium standard solution, containing 0,05 mg of cadmium per litre. Transfer, by means of a pipette, 10 ml of the cadmium standard solution (4.9) to 1 000 ml one-mark volumetric flask and dilute to the mark with water. Transfer 5 ml of this solution to another 1 0

26、00 ml one-mark volumetric flask and dilute to the mark with the dilute sulfuric acid (4.4). 1 ml of this standard solution contains 0,05 g of cadmium. 5 Apparatus The glassware used shall be washed beforehand with hot concentrated nitric acid and rinsed with water. Usual laboratory apparatus and, in

27、 particular, the following. 5.1 Round-bottom flasks, of capacity 1 000 ml. 5.2 One-mark volumetric flasks, of capacity 50 ml. 5.3 One-mark pipettes or graduated pipettes, of appropriate capacities. 5.4 Funnels and ashless filter papers. 5.5 Conical flask. 5.6 Burette, of capacity 25 ml, graduated in

28、 0,1 ml divisions. 5.7 Atomic absorption spectrometer, with a graphite furnace, a background corrector, a multipotentiometric recorder and a hollow-cathode cadmium lamp, suitable for measurements at a wavelength of 228,8 nm. 5.8 Eppendorf micropipettes, of capacities 5 l, 10 l, 20 l, 25 l and 50 l,

29、having standard colourless Eppendorf tips. Some Eppendorf micropipettes are inaccurate by 10 % or more. Unless they have been especially calibrated for this procedure, it is recommended that the same pipette be used with the test solution, blank test solution and calibration solutions. 5.9 Analytica

30、l balance. 5.10 Mechanical grinder, the internal lining and blades of which are of polytetrafluoroethylene (PTFE). BSISO65611:2005 36 Sampling A representative sample should have been sent to the laboratory. It should not have been damaged or changed during transport or storage. Sampling is not part

31、 of the method specified in this part of ISO 6561. If there is no specific International Standard dealing with the product concerned, it is recommended that the parties concerned come to an agreement on the subject. 7 Procedure 7.1 Preparation of the test sample Mix the laboratory sample well. If ne

32、cessary, first remove stones, stalks and hard seed-cavity walls and pass the laboratory sample through the mechanical grinder (5.10). Allow frozen or deep-frozen products to thaw in a closed vessel and add the liquid formed during this process to the product before mixing. 7.2 Test portion 7.2.1 Liq

33、uid products Take, by means of pipette, 10 ml of the test sample (7.1). It is also possible to take the test portion by mass by weighing a quantity of the test sample to the nearest 0,01 g. 7.2.2 Semi-solid and solid products Weigh, to the nearest 0,01 g, a quantity of the test sample (7.1) correspo

34、nding to approximately 10 g of product. 7.3 Decomposition Transfer the test portion (7.2) to a round-bottom flask (5.1). If the test portion is liquid (7.2.1) and contains ethanol, first eliminate ethanol by boiling and then allow to cool. Add 10 ml of nitric acid (4.2), heat and then carefully add

35、5 ml of concentrated sulfuric acid (4.1) Proceed as described in ISO 5515:1979, 6.3.1, from the second paragraph to the eighth paragraph. When decomposition is complete, filter the sample solution, diluted with a few millilitres of water, through an ashless filter paper (5.4) that has been previousl

36、y rinsed with hydrochloric acid and water. Collect the filtrate in a 50 ml one-mark volumetric flask (5.2), rinsing the round-bottom flask (5.1) and the filter paper with a few millilitres of water and collecting the rinsing in the same volumetric flask. Shake, allow to cool, and dilute to the mark.

37、 Mix by shaking. 7.4 Blank test Carry out a blank test by repeating the decomposition (7.3), replacing the test portion by 10 ml of water. BSISO65611:20054 7.5 Determination 7.5.1 Furnace programme The furnace shall allow four independent thermal stages: a) drying the solution; b) thermal decomposit

38、ion; c) atomization; d) increase to maximum temperature to purge the furnace. The proposed conditions are as follows: drying at 100 C for 25 s; instantaneous change to the stage of thermal decomposition at 450 C for 30 s; atomization in 7 s at 1 900 C, after a progressive increase to this temperatur

39、e. During this stage, the apparatus shall record the maximum absorbance and the variation in absorbance. The duration over which atoms exist in the furnace may be increased by decreasing the rate of circulation of nitrogen (“mini flow”) or by stopping it altogether (“gas stop”); increase to the maxi

40、mum temperature (2 700 C) to purge the furnace with nitrogen at the end of the procedure. 7.5.2 Preparation of the calibration graph Prepare calibration solutions having cadmium concentrations of 5 g/l, 10 g/l and 20 g/l by suitably diluting the cadmium standard solution (4.10). Inject successively

41、into the furnace, programmed in accordance with 7.5.1, by means of micropipette (5.8) fitted with a tip, 50 l of each of these calibration solutions. Determine the absorbance from the heights of the peaks registered. Calculate the mean value of the absorbance from the results of three injections int

42、o the furnace. The absorbances thus determined correspond, respectively, to 0,000 25 g, 0,000 5 g and 0,001 g of cadmium. Plot a calibration graph having, for example, the values of absorbances as ordinates and the corresponding cadmium concentrations as abscissae. 7.5.3 Determination of test soluti

43、on Inject successively into the furnace, programmed in accordance with 7.5.1, by means of a micropipette (5.8) fitted with a tip, three times the adequate volume of the decomposed sample solution obtained in 7.3. Note the corresponding absorbances. Calculate the mean value of the absorbance and, fro

44、m the calibration graph, read the quantity of cadmium contained in the 50 l of injected test solution. 7.5.4 Determination of the blank test solution Inject successively into the furnace, programmed in accordance with 7.5.1, by means of a micropipette (5.8) fitted with a tip, three times the adequat

45、e volume of the blank test solution (7.4). The absorbance shall be zero or less than 0,005. If necessary, subtract the mean of the three values of absorbance of the blank test solution from the mean absorbance of the test solution determined in 7.5.3 before referring to the calibration graph (7.5.2)

46、 to obtain the cadmium content of the solution. BSISO65611:2005 58 Expression of the results 8.1 Method of calculation and equations 8.1.1 Liquid products The cadmium content of the sample, expressed in milligrams per litre of product, is equal to 1 100 m (1) where m 1is the mass, in micrograms, of

47、cadmium contained in the injected volume of the test portion, read from the calibration graph. 8.1.2 Semi-solid and solid products The cadmium content of the sample, expressed in milligrams per kilogram of product, is equal to 1 0 1000 m m (2) where m 0is the mass, in grams, of the test portion (7.2

48、.2); m 1is the mass, in micrograms, of cadmium contained in the injected volume of the test portion, read from the calibration graph. 8.2 Other method of expression of results To express the cadmium content on the dry basis, modify the equations accordingly. 9 Repeatability The absolute difference b

49、etween two independent single test results, obtained using the same method on identical test material in the same laboratory by the same operator using the same equipment within a short interval of time, will in not more than 5 % of cases be greater than 10 % of the arithmetic mean of the two results. 10 Test report The test report shall specify: a) all information necessary for the complete identification of the sample; b) the samp