BS 6200-3 12 1-1986 Sampling and analysis of iron steel and other ferrous metals - Methods of analysis - Determination of copper - Steel and cast iron volumetric method《铁、钢和其他铁金属的抽.pdf
《BS 6200-3 12 1-1986 Sampling and analysis of iron steel and other ferrous metals - Methods of analysis - Determination of copper - Steel and cast iron volumetric method《铁、钢和其他铁金属的抽.pdf》由会员分享,可在线阅读,更多相关《BS 6200-3 12 1-1986 Sampling and analysis of iron steel and other ferrous metals - Methods of analysis - Determination of copper - Steel and cast iron volumetric method《铁、钢和其他铁金属的抽.pdf(8页珍藏版)》请在麦多课文档分享上搜索。
1、BRITISH STANDARD BS 6200-3.12.1: 1986 Sampling and analysis of iron, steel and other ferrous metals Part 3: Methods of analysis Section 3.12 Determination of copper Subsection 3.12.1 Steel and cast iron: volumetric method UDC 669.1:543.24:546.56BS6200-3.12.1:1986 This British Standard, having been p
2、repared under the directionof the Iron and Steel Standards Committee, was published under the authority ofthe Board of BSI and comes intoeffect on 30 September 1986 BSI 09-1999 The following BSI references relate to the work on this standard: Committee reference ISM/18 Draft for comment 85/36502 DC
3、ISBN 0 580 15279 0 Foreword This Subsection of BS6200 has been prepared under the direction of the Iron and Steel Standards Committee. It supersedes method 1 for the determination of copper in BSI Handbook No.19, to which it is technically equivalent. BS 6200 is a multipart British Standard covering
4、 all aspects of the sampling and analysis of iron, steel and other ferrous metals. A list of contents, together with general information, will be given in Part1 to be published in due course. A British Standard does not purport to include all the necessary provisions of a contract. Users of British
5、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, pagesi andii, pages1 and2, an inside back cover and a back cover. This
6、 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. Date of issue CommentsBS6200-3.12.1:1986 BSI 09-1999 i Contents Page Foreword Inside front c
7、over 1 Scope 1 2 Principle 1 3 Reagents 1 4 Apparatus 1 5 Sampling 1 6 Procedure 2 7 Calculation and expression of results 2 8 Test report 2 Publications referred to Inside back coverii blankBS6200-3.12.1:1986 BSI 09-1999 1 1 Scope This Subsection of BS6200 describes a volumetric method for the dete
8、rmination of copper in steel and cast iron. The method is applicable to copper contents exceeding0.1%m/m. NOTEThe titles of the publications referred to in this Subsection on BS6200 are listed on the inside back cover. 2 Principle In an oxidized hydrochloric acid solution of the sample, iron is redu
9、ced by boiling with sulphurous acid. Copper is precipitated as cuprous thiocyanate from a neutralized solution made slightly acid with sulphuric acid. The precipitate is filtered off, washed and dissolved in acid. The determination is completed volumetrically by releasing the iodine equivalent of th
10、e copper with potassium iodide and titrating with sodium thiosulphate. 3 Reagents During the analysis, use only reagents of recognized analytical reagent grade and only distilled water or water of equivalent purity, free from copper. 3.1 Acetic acid, glacial, density ( ) 1.048g/mL to1.050g/mL. 3.2 A
11、mmonia solution, 0.91g/mL, diluted1+1. 3.3 Copper, standard solution, corresponding to 1 mg of copper per mL. Dissolve 1.000 g of high purity copper in30mL of nitric acid (3.6). Boil to remove nitrous fumes and cool. Transfer to a1L volumetric flask, dilute to the mark and mix. 3.4 Hydrochloric acid
12、, 1.16g/mL to1.19g/mL. 3.5 Nitric acid, 1.42g/mL. 3.6 Nitric acid, 1.42g/mL, diluted2 +3. 3.7 Potassium iodide, 600 g/L solution. Dissolve 60g of potassium iodide in water, dilute to100mL and mix. 3.8 Potassium thiocyanate, 200 g/L solution. Dissolve 200g of potassium thiocyanate in water, dilute to
13、1L and mix. 3.9 Sodium fluoride 3.10 Sodium sulphite, 250 g/L solution. Dissolve 250 g of sodium sulphite in water, dilute to1L and mix. 3.11 Sodium sulphite-acid wash To 1 L of sulphuric acid (3.15) add10mL of sodium sulphite solution (3.10), 5mL of potassium thiocyanate solution (3.8) and mix. 3.1
14、2 Sodium thiosulphate, 4 g/L solution, corresponding to1mg of copper per mL. 3.12.1 Preparation. Dissolve 4 g of sodium thiosulphate pentahydrate (Na 2 S 2 O 3 .5H 2 O) in water containing0.1g of sodium carbonate. Transfer to a1L volumetric flask, dilute to the mark and mix. 3.12.2 Standardization.
15、Transfer25mL of copper solution (3.3) to a250mL conical beaker. Add10mL of sulphuric acid (3.15) and evaporate to fuming. Cool, add with care10mL of water,0.5g of sodium fluoride (3.9) and, when dissolved, add ammonia solution (3.2) until the blue colour of the cuprammonium complex is fully develope
16、d. Cool, acidify with glacial acetic acid (3.1) and add1mL excess. Cool, add 5mL of potassium iodide solution (3.7) and titrate with sodium thiosulphate solution (3.12) until the brown iodine colour is almost discharged. Add5mL of starch indicator (3.13), 10mL of potassium thiocyanate solution (3.8)
17、 and continue the titration until the blue starch-iodine colour is just discharged. Record the copper equivalent of the sodium thiosulphate solution in mg per mL. 3.13 Starch, 5 g/L solution. Make a suspension of 0.5g of starch in10mL of water. Add to90mL of boiling water. Cool, dilute to100mL and m
18、ix. 3.14 Sulphuric acid, 1.84g/mL. 3.15 Sulphuric acid, 1.84g/mL, diluted 3 +17. To 400 mL of water add cautiously150mL of sulphuric acid (3.14). Mix, cool, dilute to1L and mix. 3.16 Sulphuric acid, 1.84g/mL, diluted 1 +99. To 400 mL of water add cautiously10mL of sulphuric acid (3.14). Mix, cool, d
19、ilute to1L and mix. 3.17 Sulphurous acid Pass sulphur dioxide gas into1L of water until a saturated solution is obtained. 4 Apparatus Use ordinary laboratory apparatus. Use only volumetric glassware in accordance with class A of BS846, BS1583 or BS1792, as appropriate. 5 Sampling Sampling shall be c
20、arried out in accordance with BS1837.BS6200-3.12.1:1986 2 BSI 09-1999 NOTEBS 6200-2 “Methods of sampling and sample preparation”, which will supersede BS1837, is currently in preparation. On its publication, this Subsection will be amended to include a requirement to sample in accordance with BS6200
21、-2. 6 Procedure 6.1 Test portion Weigh, to the nearest 0.001g, a test portion in accordance with the following: a) 5 g for samples with presumed copper contents up to0.25% m/m; b) 2 g for samples with presumed copper contents between0.25% m/m and1%m/m; c) 1 g for samples with presumed copper content
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