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1、BRITISH STANDARD BS 6200-3.40.2: 1997 ISO 13898-2: 1997 Sampling and analysis of iron, steel and other ferrous metals Part 3: Methods of analysis Section 3.40 Multi-element methods Subsection 3.40.2 Determination of nickel, copper and cobalt contents by inductively coupled plasma atomic emission spe
2、ctrometric method Determination of nickel content ICS 77.080.01 Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 This British Standard, having been prepared under the direction of the Engineering Sector Board, was publishe
3、d under the authority of the Standards Board and comes into effect on 15 September 1997 BSI 09-1999 ISBN 0 580 28420 4 National foreword This British Standard reproduces verbatim ISO 13898-2:1997 and implements it as the UK national standard. The UK participation in its preparation was entrusted to
4、Technical Committee ISE/18, Sampling and analysis of iron and steel, which has the responsiblity to: aid enquirers to understand the text; present to the responsible international/European committee any enquiries on the interpretation, or proposals for change, and keep the UK interests informed; mon
5、itor related international and European developments and promulgate them in the UK. A list of organizations represented on this committee can be obtained on request to its secretary. Cross-references The British Standards which implement international or European publications referred to in this doc
6、ument 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 Catalogue. A British Standard does not purport to include all the necessary provisions of a contract. Users of
7、British Standards are responsible for their 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, pages i and ii, the ISO title page, pages ii to iv, pages 1 to
8、 5 and a back cover. This standard has been updated (see copyright date) and may have had amendments incorporated. This will be indicated in the amendment table on the inside front cover. Amendments issued since publication Amd. No.DateComments Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06
9、15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 BSI 09-1999i Contents Page National forewordInside front cover Forewordiii Text of ISO 13898-21 Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI ii blank Licensed Copy: s
10、heffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 ii BSI 09-1999 Contents Page Forewordiii 1Scope1 2Normative references1 3Principle
11、1 4Reagents1 5Apparatus1 6Sampling1 7Procedure1 8Expression of results3 9Test report3 Annex A (informative) Additional information on the international cooperative tests4 Annex B (informative) Graphical representation of precision data5 Figure B.1 Logarithmic relationship between nickel content () a
12、nd repeatability limit (r) or reproducibility limits (R and Rw)5 Table 1 Nickel contents between 0,001 % (m/m) and 0,30 % (m/m)2 Table 2 Example for nickel contents up to 0,010 % (m/m)2 Table 3 Example for nickel contents between 0,010 % (m/m) and 0,060 % (m/m)3 Table 43 Table A.14 Descriptors: Iron
13、 and steel products, unalloyed steels, unalloyed cast iron, chemical analysis, determination of content, nickel, spectrometric method, atomic emission spectrometric method. wNi Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1
14、997 BSI 09-1999iii 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 interested in a su
15、bject 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 (
16、IEC) on all matters of electrotechnical standardization. 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. International St
17、andard ISO 13898-2 was prepared by Technical Committee ISO/TC 17, Steel, Subcommittee SC 1, Methods of determination of chemical composition. ISO 13898 consists of the following parts, under the general title Steel and iron Determination of nickel, copper and cobalt contents Inductively coupled plas
18、ma atomic emission spectrometric method. Part 1: General requirements and sample dissolution; Part 2: Determination of nickel content; Part 3: Determination of copper content; Part 4: Determination of cobalt content. Annex A and Annex B of this part of ISO 13898 are for information only. Licensed Co
19、py: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI iv blank Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 BSI 09-19991 1 Scope This part of ISO 13898 specifies an inductively
20、 coupled plasma atomic emission spectrometric method for the determination of nickel content in unalloyed steel and unalloyed iron. The method is applicable to nickel contents between 0,001 % (m/m) and 0,30 % (m/m). 2 Normative references The following standards contain provisions which, through ref
21、erence in this text, constitute provisions of this part of ISO 13898. At the time of publication, the editions indicated were valid. All standards are subject to revision, and parties to agreements based on this part of ISO 13898 are encouraged to investigate the possibility of applying the most rec
22、ent editions of the standards indicated below. Members of IEC and ISO maintain registers of currently valid International Standards. ISO 3696:1987, Water for analytical laboratory use Specification and test methods. ISO 5725-1:1994, Accuracy (trueness and precision) of measurement methods and result
23、s Part 1: General principles and definitions. ISO 5725-2:1994, Accuracy (trueness and precision) of measurement methods and results Part 2: Determination of repeatability and reproducibility of a standard measurement method. ISO 5725-3:1994, Accuracy (trueness and precision) of measurement methods a
24、nd results Part 3: Intermediate measures of the precision of a standard measurement method. ISO 13898-1:1997, Steel and iron Determination of nickel, cobalt and copper contents Inductively coupled plasma atomic emission spectrometric method Part 1: General requirements and sample dissolution. ISO 14
25、284:1996, Steel and iron Sampling and preparation of samples for the determination of chemical composition. 3 Principle The principle is described in clause 3 of ISO 13898-1:1997. 4 Reagents During the analysis, unless otherwise stated, use only reagents of recognized analytical grade and only grade
26、 2 water as specified in ISO 3696. In addition to the reagents given in clause 4 of ISO 13898-1:1997, the following are required. 4.1 Nickel standard solution 4.1.1 Stock solution, corresponding to 1,0 g of nickel per litre. Weigh, to the nearest 0,1 mg, 1,000 g of nickel metal purity 99,9 % (m/m) a
27、nd transfer to a 200 ml beaker. Add 50 ml of nitric acid (4.3 of ISO 13898-1:1997) cover with a watch-glass and heat to dissolve gently. Cool to ambient temperature, quantitatively transfer to a 1 000 ml one-mark volumetric flask and dilute to the mark with water and mix. 1 ml of this stock solution
28、 contains 1,0 mg Ni. 4.1.2 Standard solution A, corresponding to 0,100 g of nickel per litre. Transfer 20,0 ml of the nickel stock solution (4.1.1) to a 200 ml one-mark volumetric flask, dilute to the mark with water and mix. Prepare this standard solution immediately before use. 1 ml of this standa
29、rd solution contains 0,10 mg Ni. 4.1.3 Standard solution B, corresponding to 0,020 g of nickel per litre. Transfer 10,0 ml of the nickel stock solution (4.1.1) to a 500 ml one-mark volumetric flask, dilute to the mark with water and mix. If the calibration graph is found to be non-linear, additional
30、 calibration series may be used. Prepare this standard solution immediately before use. 1 ml of this standard solution contains 0,020 mg Ni. 5 Apparatus The apparatus required is given in clause 5 of ISO 13898-1:1997. 6 Sampling Carry out sampling in accordance with ISO 14284. 7 Procedure 7.1 Test p
31、ortion Weigh, to the nearest 1 mg, about 1,00 g of the test sample. 7.2 Blank test (corresponding to the zero member) Proceed as directed in 7.2 of ISO 13898-1:1997. 7.3 Determination 7.3.1 Preparation of the test solution Proceed as directed in 7.3.1 of ISO 13898-1:1997. Licensed Copy: sheffieldun
32、sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 2 BSI 09-1999 7.3.2 Preparation of the calibration solutions Transfer to a series of six 200 ml beakers 1,00 g 0,001 g of the pure iron (4.1 of ISO 13898-1:1997). Add to each beaker 10 ml of nitric ac
33、id (4.3 of ISO 13898-1:1997), cover the beaker with a watch-glass and heat gently until the end of effervescence. Add 10 ml of hydrochloric acid (4.2 of ISO 13898-1:1997) and continue the heating until complete dissolution occurs. Cool to ambient temperature and transfer the solution to six 200 ml o
34、ne-mark volumetric flasks, rinsing the beakers with the minimum quantity of water. Using a pipette or burette, add to the volumetric flasks the volume of nickel standard solution A (4.1.2) indicated in Table 1. If the calibration graph is found to be non-linear, additional calibration series may be
35、used (e.g. Table 2 and Table 3). If the internal standard technique is used, using a pipette, add 2 ml of the scandium internal standard solution (4.4 of ISO 13898-1:1997) or 10 ml of the yttrium internal standard solution (4.5 of ISO 13898-1:1997). Dilute to the mark with water and mix. 7.4 Spectro
36、metric measurements 7.4.1 Optimization of the instrument Proceed as directed in 7.4.1 of ISO 13898-1:1997. 7.4.2 Measurements of the emitted intensities Proceed as directed in 7.4.2 of ISO 13898-1:1997. 7.4.3 Preparation of the calibration graph Proceed as directed in 7.4.3 of ISO 13898-1:1997. Tabl
37、e 1 Nickel contents between 0,001 % (m/m) and 0,30 % (m/m) Table 2 Example for nickel contents up to 0,010 % (m/m) Volume of nickel standard solution A (4.1.2) Nickel concentrationCorresponding nickel content in the test portion ml4g/ml% (m/m) 0a 5,0 10,0 15,0 20,0 30,0 0 2,50 5,00 7,50 10,00 15,00
38、0 0,050 0,100 0,150 0,200 0,300 a Zero member. Volume of nickel standard solution B (4.1.3) Nickel concentrationCorresponding nickel content in the test portion ml4g/ml% (m/m) 0a 0,5 1,0 2,0 3,0 5,0 0 0,050 0,100 0,200 0,300 0,500 0 0,001 0 0,002 0 0,004 0 0,006 0 0,010 0 a Zero member. Licensed Cop
39、y: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 BSI 09-19993 Table 3 Example for nickel contents between 0,010 % (m/m) and 0,060 % (m/m) Table 4 8 Expression of results 8.1 Method of calculation Proceed as directed in 8.1 of ISO 1389
40、8-1:1997. 8.2 Precision A planned trial of this method was carried out by 26 laboratories in 12 countries at 11 levels of nickel, each laboratory making three determinations of nickel content at each level (see notes 1 and 2). The test samples used are listed in Table A.1. The results obtained were
41、treated statistically in accordance with ISO 5725-1, ISO 5725-2 and ISO 5725-3, using the data obtained from the samples containing 11 levels of nickel within the application range. The data obtained showed a logarithmic relationship between nickel content and repeatability limit (r) and reproducibi
42、lity limits (R and Rw) of the test results (see note 3), as summarized in Table 4. The graphical representation of the data is given in Annex B. NOTE 1Two of the three determinations were carried out under repeatability conditions as defined in ISO 5725-1, i.e. one operator, same apparatus, identica
43、l operating conditions, same calibration, and a minimum period of time. NOTE 2The third determination was carried out at a different time (on a different day) by the same operator as in note 1 using the same apparatus with a new calibration. NOTE 3From the results obtained on day 1 the repeatability
44、 limit (r) and reproducibility limit (R) were calculated using the procedure specified in ISO 5725-2. From the first result obtained on day 1 and the result obtained on day 2, the within-laboratory reproducibility limit (Rw) was calculated using the procedure given in ISO 5725-3. 9 Test report Proce
45、ed as directed in clause 9 of ISO 13898-1:1997. Volume of nickel standard solution B (4.1.3) Nickel concentrationCorresponding nickel content in the test portion ml4g/ml% (m/m) 0a 0,5 10,0 20,0 30,0 50,0 0 0,50 1,00 2,00 3,00 5,00 0 0,010 0,020 0,040 0,060 0,100 a Zero member. Nickel contentRepeatab
46、ility limitReproducibility limits % (m/m)rRRw 0,001 0,002 0,005 0,010 0,020 0,050 0,000 39 0,000 46 0,000 56 0,000 66 0,000 77 0,000 95 0,000 76 0,000 95 0,001 3 0,001 6 0,002 0 0,002 8 0,000 55 0,000 67 0,000 87 0,001 0 0,001 3 0,001 6 0,050 0,100 0,200 0,300 0,001 3 0,002 6 0,005 1 0,007 5 0,003 7
47、 0,007 4 0,015 0,023 0,002 0 0,003 7 0,007 0 0,010 Licensed Copy: sheffieldun sheffieldun, na, Wed Dec 06 15:09:28 GMT+00:00 2006, Uncontrolled Copy, (c) BSI BS 6200-3.40.2:1997 4 BSI 09-1999 Annex A (informative) Additional information on the international cooperative tests The repeatability and re
48、producibility data in Table 4 were derived from the results of international analytical trials carried out in 1993 on nine steel samples and two iron samples in 12 countries involving 26 laboratories. The results of the trials were reported in document ISO/TC 17/SC 1 N 1024, March 1994. The graphica
49、l presentation of the precision data is given in Annex B. The test samples used are listed in Table A.1. Table A.1 SampleNickel content % (m/m) Precision data CertifiedFoundRepeatability limit Reproducibility limits rRRw JSS 003-3 (Unalloyed steel) 0,000 80,000 760,000 760,000 490,000 750,000 53 NR 1C (Unalloyed steel) 0,009 00,009 00,008 90,000 430,001 40,001 0 NR 21 (Unalloyed steel) 0,0350,034 60,034 50,001 10,003 60,001 3 NBS 15h (Unalloyed steel) 0,0170,017 80,017 80,000 690,002 30,001 1 NBS 16f (Unalloyed steel)