BS 5766-21-2001 Methods for analysis of animal feeding stuffs Determination of potassium and sodium contents Methods using flame-emission spectrometry《动物饲料分析方法 钠钾含量的测定 使用火焰发射光谱法》.pdf

《BS 5766-21-2001 Methods for analysis of animal feeding stuffs Determination of potassium and sodium contents Methods using flame-emission spectrometry《动物饲料分析方法 钠钾含量的测定 使用火焰发射光谱法》.pdf》由会员分享，可在线阅读，更多相关《BS 5766-21-2001 Methods for analysis of animal feeding stuffs Determination of potassium and sodium contents Methods using flame-emission spectrometry《动物饲料分析方法 钠钾含量的测定 使用火焰发射光谱法》.pdf（18页珍藏版）》请在麦多课文档分享上搜索。

1、BRITISH STANDARD BS 5766-21:2001 BS ISO 7485:2000 Methods for analysis of animal feeding stuffs Part 21: Determination of potassium and sodium contents Methods using flame-emission spectrometry ICS 65.120 NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBS 5766-21:2001 This Brit

2、ish Standard, having been prepared under the direction of the Consumer Products and Services Sector Committee, was published under the authority of the Standards Committee and comes into effect on 15 May 2001 BSI 05-2001 ISBN 0 580 37280 4 National foreword This British Standard reproduces verbatim

3、ISO 7485:2000 and implements it as the UK national standard. The UK participation in its preparation was entrusted to Technical Committee AW/10, Animal feeding stuffs, which has the responsibility to: A list of organizations represented on this committee can be obtained on request to its secretary.

4、Cross-references The British Standards which implement international publications referred to in this document may be found in the BSI Standards Catalogue under the section entitled “International Standards Correspondence Index”, or by using the “Find” facility of the BSI Standards Electronic Catalo

5、gue. A British Standard does not purport to include all the necessary provisions of a contract. Users of British Standards are responsible for their correct application. Compliance with a British Standard does not of itself confer immunity from legal obligations. aid enquirers to understand the text

6、; present to the responsible international/European committee any enquiries on the interpretation, or proposals for change, and keep the UK interests informed; monitor related international and European developments and promulgate them in the UK. Summary of pages This document comprises a front cove

7、r, an inside front cover, the ISO title page, pages ii and iii, a blank page, pages 1 to 10, an inside back cover and a back cover. The BSI copyright date displayed in this document indicates when the document was last issued. Amendments issued since publication Amd. No. Date CommentsReference numbe

8、r ISO 7485:2000(E) INTERNATIONAL STANDARD ISO 7485 First edition 2000-08-15 Animal feeding stuffs Determination of potassium and sodium contents Methods using flame-emission spectrometry Aliments des animaux Dtermination des teneurs en potassium et sodium Mthodes par spectromtrie dmission de flammeI

9、SO7485:2000(E) ii ISO 7485:2000(E)iii Foreword 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

10、 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 Electrotec

11、hnical Commission (IEC) on all matters of electrotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 3. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publ

12、ication 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 International Standard may be the subject of patent rights. ISO shall not be held responsible for identifying any or al

13、l such patent rights. International Standard ISO 7485 was prepared by Technical Committee ISO/TC 34, Agricultural food products, Subcommittee SC 10, Animal feeding stuffs. Annex A of this International Standard is for information only.INTERNATIONAL STANDARD ISO 7485:2000(E)1 Animal feeding stuffs De

14、termination of potassium and sodium contents Methods using flame-emission spectrometry 1 Scope This International Standard specifies a calibration method and a standard addition method for the determination of potassium and sodium contents of animal feeding stuffs by flame-emission spectrometry. The

15、 standard addition method applies if it is not known whether the emissions measured for potassium or sodium are subject to matrix effects. The limit of determination for potassium and sodium is 0,04 g/kg. The calibration method applies if such matrix effects have been shown to be absent. 2 Normative

16、 reference The following normative document contains provisions which, through reference in this text, constitute provisions of this International Standard. For dated references, subsequent amendments to, or revisions of, any of these publications do not apply. However, parties to agreements based o

17、n this International Standard are encouraged to investigate the possibility of applying the most recent edition of the normative document indicated below. For undated references, the latest edition of the normative document referred to applies. Members of ISO and IEC maintain registers of currently

18、valid International Standards. ISO 6498:1998, Animal feeding stuffs Preparation of test samples. 3P r i n c i p l e The test portion is incinerated to destroy any organic matter. The potassium and sodium are dissolved by treatment with hydrochloric acid. The potassium and sodium contents are determi

19、ned by flame-emission spectrometry at wavelengths of 766 nm and 589 nm respectively, by means of a calibration curve (calibration method) or a standard addition graph (standard addition method). 4 Reagents Use only reagents of recognized analytical quality. 4.1 Water, double distilled, or double dei

20、onized. 4.2 Potassium chloride (KCl), dried for 2 h at (110 2) C. 4.3 Sodium chloride (NaCl), dried for 2 h at (110 2) C. 4.4 Concentrated hydrochloric acid, c(HCl) = 12 mol/l ( 20 (HCl) = 1,19 g/ml). 4.5 Hydrochloric acid, c(HCl) = 6 mol/l. 4.6 Dilute hydrochloric acid, c(HCl) = 0,1 mol/l.ISO 7485:

21、2000(E) 2 4.7 Ionization and release buffer solution. Dissolve 50 g of caesium chloride and 250 g of aluminium nitrate nonahydrate Al(NO 3 ) 3 9H 2 O in water. Dilute to 1 litre with water and mix. Store in a plastic bottle, e.g. polyethene or polypropylene. 4.8 Potassium standard solutions. 4.8.1 P

22、otassium stock solution, (K) = 1 mg/ml. Weigh 1,906 g of potassium chloride (4.2) and transfer to a 1 000 ml volumetric flask with approximately 250 ml of dilute hydrochloric acid (4.6). Dissolve and dilute to the mark with the hydrochloric acid (4.6). Store in a plastic bottle, e.g. polyethene or p

23、olypropylene. At room temperature the solution is stable for up to 6 months. 4.8.2 Potassium intermediate solution, (K) = 100 g/ml. Transfer 10 ml of the potassium stock solution (4.8.1) to a 100 ml volumetric flask. Dilute to the mark with dilute hydrochloric acid (4.6) and mix. Store in a plastic

24、bottle, e.g. polyethene or polypropylene. At room temperature the solution is stable for 1 month. 4.8.3 Potassium calibration solution, (K) = 10 g/ml. Transfer 10 ml of the potassium intermediate solution (4.8.2) to a 100 ml volumetric flask. Add 10 ml of the ionization and release buffer solution (

25、4.7). Dilute to the mark with dilute hydrochloric acid (4.6) and mix. Prepare fresh on the day of use. 4.9 Sodium standard solutions. 4.9.1 Sodium stock solution, (Na) = 1 mg/ml. Weigh 2,542 g of sodium chloride (4.3) and transfer to a 1 000 ml volumetric flask with approximately 250 ml of dilute hy

26、drochloric acid (4.6). Dissolve and dilute to the mark with the hydrochloric acid (4.6). Mix well. Store in a plastics bottle. At room temperature the solution is stable for up to 6 months. 4.9.2 Sodium intermediate solution, (Na) = 100 g/ml. Transfer 10 ml of the sodium stock solution (4.9.1) to a

27、100 ml volumetric flask. Dilute to the mark with dilute hydrochloric acid (4.6) and mix. Store in a plastics bottle. At room temperature the solution is stable for 1 month. 4.9.3 Sodium calibration solution, (Na) = 10 g/ml. Transfer 10 ml of the sodium intermediate solution (4.9.2) to a 100 ml volum

28、etric flask. Add 10 ml of the ionization and release buffer solution (4.7). Dilute to the mark with the hydrochloric acid (4.6) and mix. Prepare fresh on the day of use. 4.10 Biological Certified Reference Materials. For example: V8-Rye flour or V10-Hay (powdered), from the International Atomic Ener

29、gy Agency (IAEA), Austria; SRM 157-Wheat flour, SRM 1568a-Rice flour or SRM 1548-Total diet, from the National Institute of Standards and Technology (NIST), USA.ISO 7485:2000(E)3 5 Apparatus Usual laboratory equipment and, in particular, the following. 5.1 Analytical balance, capable of weighing to

30、the nearest 1 mg. 5.2 Muffle furnace, electrically heated, capable of being maintained at (550 20) C. 5.3 Ashing dishes, of platinum or silica. 5.4 Flame photometer with an air-butane, air-propane or air-acetylene flame in a ratio allowing complete combustion; or an atomic absorption spectrometer op

31、erating in emission mode and equipped to determine potassium and sodium with an air-acetylene flame. 5.5 Sand bath or hot plate, capable of being maintained at approximately 150 C. 5.6 TD (to deliver) precision pipettes or microburette of 5 ml capacity. 5.7 TC (to contain) precision pipettes, of var

32、ious capacities. 5.8 Beakers, of 250 ml capacity. 5.9 Volumetric flasks, of various capacities. 6 Sampling Sampling is not part of the method specified in this International Standard. A recommended sampling method is given in ISO 6497 1. It is important that the laboratory receive a sample which is

33、truly representative and has not been damaged or changed during transport or storage. 7 Preparation of test sample Prepare the test sample in accordance with ISO 6498. 8 Procedure 8.1 Test portion 8.1.1 Samples containing organic matter Depending on the expected content, weigh 1 g to 5 g of the prep

34、ared test sample (clause 7) to the nearest 1 mg into an ashing dish (5.3). Proceed in accordance with 8.2.1. 8.1.2 Samples not containing organic matter Depending on the expected content of potassium and sodium, weigh 1 g to 5 g of the prepared test sample to the nearest 1 mg into a beaker (5.8). Pr

35、oceed in accordance with 8.2.2.ISO 7485:2000(E) 4 8.2 Preparation of test solution 8.2.1 Incineration and rendering silica insoluble Place the incineration dish containing the test portion (8.1.1) in the cold muffle furnace (5.2). Close the furnace and gradually increase the temperature to 550 C and

36、 ash for 3 h at this temperature. If many carbon particles are present, allow to cool down, moisten the contents of the dish with 2 ml of water and dry the dish on the sand bath or hot plate (5.5). Ash for another 2 h at 550 C in the muffle furnace. Allow to cool down, moisten the ash with a few dro

37、ps of water and transfer it to a 250 ml beaker (5.8). Rinse the incineration dish with a total of approximately 5 ml of concentrated hydrochloric acid (4.4) and then with a few millilitres of water, collecting the rinsings in the beaker. CAUTION Take care during the addition of hydrochloric acid, as

38、 an effervescent reaction may occur with some samples. Put a watch glass on the beaker to reduce spattering and slowly evaporate the contents of the beaker to near dryness on the sand bath or hot plate (5.5). Allow to cool to room temperature. Proceed in accordance with 8.2.3. 8.2.2 Dissolution of p

39、otassium and sodium Add to the beaker containing the test portion (8.1.2), slowly and carefully, a sufficient quantity (15 ml to 30 ml) of concentrated hydrochloric acid (4.4). Put a watch glass on the beaker to reduce spattering and slowly evaporate the contents of the beaker to dryness on the sand

40、 bath or hot plate (5.5). Allow to cool to room temperature. 8.2.3 Re-dissolution of potassium and sodium Treat the residue (8.2.1 or 8.2.2) with 5 ml of hydrochloric acid (4.5) and 45 ml of water. Bring to the boil and allow to cool to room temperature. Transfer quantitatively into a 100 ml volumet

41、ric flask. Dilute to the mark with water and mix. Allow particles to settle for at least 4 h. Filter if the solution is not clear. CAUTION Perform the above operations in an effective fume-removal device. 8.3 Blank test solution Prepare a solution in the same way as for the test solution, carrying o

42、ut all the operations specified in 8.2 but omitting the test portion. 8.4 Selection of method If it is not known whether the emissions measured for potassium or sodium are subject to matrix effects, proceed in accordance with 8.6. If such matrix effects have been shown to be absent, proceed in accor

43、dance with 8.5. 8.5 Calibration method 8.5.1 Test solutions Transfer to a 100 ml volumetric flask an aliquot portion of the test solution (8.2.3) containing a maximum of 1 mg of potassium or sodium. Add 10 ml of the ionization and release buffer solution (4.7), dilute to the mark with water and mix.

44、 Prepare the same dilution of the blank test solution (8.3) in the same way.ISO 7485:2000(E)5 8.5.2 Calibration solutions Transfer to six 100 ml volumetric flasks 0 ml, 2,0 ml, 4,0 ml, 6,0 ml, 8,0 ml and 10,0 ml of the potassium intermediate solution (4.8.2) or sodium intermediate solution (4.9.2).

45、Add 10 ml of the ionization and release buffer solution (4.7) to each flask. Dilute to the mark with hydrochloric acid (4.6) and mix. The potassium or sodium contents of these solutions are 0 g/ml, 2,0 g/ml, 4,0 g/ml, 6,0 g/ml, 8,0 g/ml and 10,0 g/ml respectively. Prepare fresh on the day of use. 8.

46、5.3 Spectrometric measurements 8.5.3.1 Adjustment of the instrument Adjust the instrument in accordance with the manufacturers instructions. Light the flame and allow some minutes for flame stabilization. Adjust the burner position, the gas flows and the wavelengths (theoretically 766 nm for potassi

47、um and 589 nm for sodium) or select the filters so that maximum reading is obtained when the calibration solution of potassium (4.8.3) or sodium (4.9.3) is atomized in the flame. 8.5.3.2 Test solution measurements Measure the emissions of the calibration solutions (8.5.2) and then the emission of th

48、e test solution (8.5.1). Correct the emission of the test solution for the emission of the diluted blank test solution (8.5.1), if the latter differs from the emission of the zero concentration calibration solution. 8.5.4 Calibration graph Draw the calibration graph by plotting the emissions of the

49、calibration solutions against their respective potassium or sodium contents in micrograms per millilitre. 8.6 Standard addition method 8.6.1 Test solutions Carry out the dilutions according to the expected potassium or sodium content. Transfer to each of three volumetric flasks of suitable capacity (flasks A, B and C) the same aliquot portion of the test solution (8.2.3). Add to flasks B and C aliquot portions of the potassium intermediate solution (4.8.2) or sodium intermediate solution (4.9.2) corresponding to a c