ISO 1553-1976 Unalloyed copper containing not less than 99 90 % of copper Determination of copper content Electrolytic method《纯铜(铜≥99 90%) 铜含量的测定 电解法》.pdf

《ISO 1553-1976 Unalloyed copper containing not less than 99 90 % of copper Determination of copper content Electrolytic method《纯铜(铜≥99 90%) 铜含量的测定 电解法》.pdf》由会员分享，可在线阅读，更多相关《ISO 1553-1976 Unalloyed copper containing not less than 99 90 % of copper Determination of copper content Electrolytic method《纯铜(铜≥99 90%) 铜含量的测定 电解法》.pdf（6页珍藏版）》请在麦多课文档分享上搜索。

1、INTERNATIONAL STANDARD 1553 INTERNATIONAL ORGANIZATION FOR STANDARDIZATION MEY,!WHAPOHAI OPrAHM3AUMR n0 CTAHAPTM3AUM.ORGANISATION INTERNATIONALE DE NORMALISATON Unalloyed copper containing not less than 99,90 % of copper - Determination of copper content - Electrolytic method Cuivres non alli these

2、documents are in the process of being transformed into International Standards. As part of this process, Technical Committee ISO/TC 26, Copper and copper alloys, has reviewed IS0 Recommen- dation R 1553-1971 and found it technically suitable for transformation. International Standard IS0 1553 theref

3、ore replaces IS0 Recommen- dation R 1553-l 971, to which it is technically identical. IS0 Recommendation R 1553 had been approved by the member bodies of the following countries : Australia Belgium Canada Cuba Czechoslovakia Egypt, Arab Rep. of Finland France Germany Hungary India I ran Israel Italy

4、 Japan Netherlands New Zealand Norway Peru Poland South Africa, Rep. of Spain Sweden Switzerland Thailand Turkey United Kingdom U.S.A. Yugoslavia No member body had expressed disapproval of the Recommendation. The member bodies of the following countries disapproved the transformation of the Recomme

5、ndation into an International Standard : Hungary Italy 0 international Organization for Standardization, 1976 l Printed in Switzerland Copyright International Organization for Standardization Provided by IHS under license with ISONot for ResaleNo reproduction or networking permitted without license

6、from IHS-,-,-INTERNATIONAL STANDARD ISO 1553-1976 (E) Unalloyed copper containing not less than 99,90 % of copper - Determination of copper content - Electrolytic method 1 SCOPE AND FIELD OF APPLICATION This International Standard specifies an electrolytic method for the determination of the copper

7、content of unalloyed copper containing not less than 99,90 % of copper. Silver, if present, is deposited with the copper and is reported as copper. The method is applicable to coppers free from elements which leave insoluble residues in the solution for electrolysis, and having a low content of impu

8、rities which can be deposited electrolytically together with the copper. A spectrophotometric method for the determination of residual copper in the electrolyte after deposition of copper on the cathode is given in annex B. 2 REFERENCE ISO/R 1811, Chemical analysis of copper and copper alloys - Samp

9、ling of copper refinery shapes. 3 PRINCIPLE Electrolytic determination of the copper content of a sulphuric/nitric acid solution of a test portion. 4 REAGENTS During the analysis, use only reagents of recognized analytical grade and only distilled or deionized water. 4.1 Sulphuric/nitric acid, solut

10、ion. Add slowly, while stirring, 300 ml of sulphuric acid, p approximately I,83 g/ml, to 750 ml of water. Cool, and add 210 ml of nitric acid, p approximately I,38 g/ml. 5 APPARATUS Ordinary laboratory apparatus and 5.1 Current source. For preference, use a 6 V accumulator. If a rectifier is to be u

11、sed, an additional buffer battery is recommended. 5.2 Electrolysis equipment, the electrodes of which meet the following requirements : 5.2.1 Platinum cathode, Winkler type), made preferably from gauze containing approximately 400 meshes per square centimetre (50 meshes per linear inch), woven from

12、wire of diameter approximately 0,20 mm. The cathode shall be stiffened by doubling the gauze for about 3 mm at the top and the bottom of the cylinder or by reinforcing the gauze at the top and bottom with a platinum band or ring. The diameter of the cylinder shall be 30 to 50 mm and the height 40 to

13、 60 mm. The stem shall be made from a platinum alloy wire, such as platinum-iridium, platinum- rhodium, or platinum-ruthenium, having a diameter of approximately I,30 mm, flattened and welded along the entire length of the gauze. The overall height of the cathode shall be approximately 130 mm. The c

14、athode shall be sandblasted. 5.2.2 Spiral anode, made of platinum alloy wire of minimum diameter 1 mm, formed into a spiral of seven turns, having a height of approximately 50 mm and a diameter of 12 mm, the overall height being approximately 130 mm. The spiral section of the +anode shall be sandbla

15、sted. 5.3 Electric oven, capable of being controlled at 110 “C. 6 SAMPLING Sampling shall be carried out according to the procedure given in ISO/R 1811. 7 PROCEDURE 7.1 Test portion Weigh, to the nearest 0,001 g, 5 g of the test sample (see annex A). 7.2 Determination 7.2.1 Transfer the test portion

16、 (7.1) to a 400 ml tall-form lipless beaker provided with a close-fitting watch glass. Add 1) Platinum cathodes formed from plain or perforated sheets may also be used. 1 Copyright International Organization for Standardization Provided by IHS under license with ISONot for ResaleNo reproduction or n

17、etworking permitted without license from IHS-,-,-is0 1553-1976 03 45 ml of the sulphuric/nitric acid solution (4.1) and allow to stand for a few minutes until the reaction has nearly ceased. Heat at a temperature of 80 to 90 “C to complete dissolution and maintain the solution at this temperature fo

18、r 2 to 3 h to expel the oxides of nitrogen quantitatively. Wash the watch glass and walls of the beaker, and dilute the solution to 300 ml. 7.2.2 Insert the electrodes (5.2.1 and 5.2.2) in the solution and cover the beaker with two halves of a watch glass, one of which has two indentations through w

19、hich the electrode stems may pass. Electrolyse, without stirring, at a current density of about 0.6 A per square decimetre of cathode surface. When the solution becomes colourless, reduce the current density to about 0,3 Afdm2 and wash the watch glasses, electrode stems, and walls of the beaker. Con

20、tinue the electrolysis until the deposition of the copper is complete, as indicated by failure to plate on an unplated surface of the electrode stem when the level of the solution is raised. 7.2.3 Without switching off the current, quickly replace the beaker by another of the same size containing ap

21、proximately 350 ml of distilled water. Continue the electrolysis for 15 min. Remove the cathode and dip it in ethanol or methanol. Dry in the oven (5.3). maintained at 110 OC, for 3 to 5 min and cool, Determine the mass of the deposit of metallic copper as indicated in annex A. 7.2.4 Verify the abse

22、nce of copper in the electrolyte by a calorimetric test; if the determined content of copper is less than or equal to the prescribed figure, determine the residual copper in the electrolyte in accordance with the method given in annex B. 8 EXPRESSION OF RESULTS 8.1 Method of calculation The copper c

23、ontent is given, as a percentage by mass, by the formula where XIOO m m. is the mass, in grams, of the test portion (7.1); ml is the mass, in grams, of copper deposited. 8.2 Repeatability The determination shall be carried out twice, and the results obtained shall agree within 0,015 % (m/m) of coppe

24、r. 9 TEST REPORT The test report shall include the following particulars : a) the reference of the method used; b) the results and the method of expression used; c) any unusual features noted during the determination; d) any operation not included in this International Standard or in the document to

25、 which reference is made, or regarded as optional. ANNEX A DETERMINATION OF MASS OF TEST PORTION AND COPPER DEPOSIT A.1 USING A TWO-PAN BALANCE A.2 USING A SINGLE-PAN BALANCE Using a marked 5 g weight, weigh 5,005 0 to 5,007 0 g of the test sample, this mass constituting the test portion. Weigh the

26、cathode, placing the marked 5 g weight used in weighing the test portion on the same balance-pan as the cathode, and noting the other weights used. Deduct 5 g from the observed mass to obtain the mass of the cathode. Weigh the cathode with the copper deposit, using the same weights as were used in w

27、eighing the cathode before the electrolysis, except that the marked 5 g weight used on the pan with the cathode shall be omitted. First weigh the cathode alone and then, without removing the cathode from the balance, weigh accurately about 5 g of the test sample, this mass constituting the test port

28、ion. In subsequent weighing of the cathode with the copper deposit, use the same weights. The mass of the test portion is the difference between the masses of the cathode plus the test portion and the cathode alone. The mass of the copper deposit is the difference between the masses of the cathode w

29、ith the deposit and the cathode alone. 2 Copyright International Organization for Standardization Provided by IHS under license with ISONot for ResaleNo reproduction or networking permitted without license from IHS-,-,-IS0 1553-1976 (El ANNEX B DETERMINATION OF RESIDUAL COPPER IN THE ELECTROLYTE - S

30、PECTROPHOTOMETRIC METHOD B.l SCOPE AND FIELD OF APPLICATION This annex specifies a spectrophotometric method for the determination of copper content. The method is applicable to the determination of residual copper in the electrolyte after the deposition of copper on the cathode. B.2 PRINCIPLE Forma

31、tion of the copper-oxalyl dihydrazide complex at pH 8,8 in the presence of acetaldehyde. Spectrophotometric measurement at a wavelength of approximately 540 nm. B.3 REAGENTS During the analysis, use only reagents of recognized analytical grade and only distilled or deionized water. 8.3.1 Ammonia sol

32、ution, p approximately 0,91 g/ml. B.3.2 Sulphuric/nitric acid solution. For the preparation, see 4.1. 8.3.3 Citric acid, 200 g/l solution. B.3.4 Acetaldehyde, 40 % (m/m) solution in water or methanol. B.3.5 Oxalyl dihydrazide, 2,50 g/l solution. Dissolve 2,50 g of oxalyl dihydrazide (H,NNH(CO),) in

33、1 I of water, heating gently. B.3.6 Copper, 0.01 g/l standard solution. In a 250 ml beaker, dissolve 1 g of electrolytic copper in 10 ml of nitric acid, p approximately I,38 g/ml, diluted with an equal volume of water. Evaporate almost to dryness to remove the excess acid. Add 50 ml of water to diss

34、olve the residue. Transfer to a 1 000 ml one-mark volumetric flask, rinse the beaker and dilute to the mark with water. Transfer 10 ml of this solution to a 1 000 ml one-mark volumetric flask and dilute to the mark with water. 1 ml of this standard solution contains 0,010 mg of Cu. B.4 APPARATUS Ord

35、inary laboratory apparatus and B.4.1 Spectrophotome;er, suitable for measurements at a wavelength of approximately 540 nm. B.5 PROCEDURE B.5.1 Determination After weighing the deposit of cathodic copper, concentrate the electrolyte to approximately 200 ml, cool and transfer to a 250 ml one-mark volu

36、metric flask. Dilute to the mark with water. Transfer 10 ml of this solution to a 50 ml one-mark volumetric flask. Add in the following order, shaking after each addition, - 2 ml of the citric acid solution (B.3.3); - 11 ml of the ammonia solution (B.3.1); - 10 ml of the acetaldehyde solution (B.3.4

37、); - 10 ml of the oxalyl dihydrazide solution (8.3.5). Cool, dilute to the mark with water and allow to stand for 30 min. Make the spectrophotometric measurement of this solution at a wavelength of approximately 540 nm after having adjusted the spectrophotometer (B.4.1) to zero absorbance against th

38、e zero term of the calibration graph.1) B.5.2 Plotting the calibration graph Transfer 45 ml of the sulphuric/nitric acid solution (B.3.2) to a 250 ml one-mark volumetric flask. Dilute to the mark with water. Place 10 ml of this solution into each of a series of six 50 ml one-mark volumetric flasks.

39、Add the following amounts of the standard copper solution (B.3.6) : 0 -1 - 2 - 3 - 4 and 5 ml, corresponding respectively to 0 - 0,Ol - 0,02 - 0,03 - 0,04 and 0.05 mg of copper. 1 j The zero term of the calibration graph corresponds to the blank test of the reagents. 3 Copyright International Organi

40、zation for Standardization Provided by IHS under license with ISONot for ResaleNo reproduction or networking permitted without license from IHS-,-,-IS0 1553-1976 (El Continue as indicated in paragraphs 3 and 4 of B.5.1 and make the spectrophotometric measurements of the standard matching solutions a

41、t a wavelength of approximately 540 nm after having adjusted the spectro- photometer (B.4.1) to zero absorbance against the zero term of the graph. B.7 TEST REPORT The test report shall include the following particulars : a) the reference of the method used; Plot the calibration graph b) the results

42、 and the method of expression used; B.6 EXPRESSION OF RESULTS c) any unusual features noted during the determination; From the calibration graph, deduce the mass of residual d) any operation not included in this international copper in the electrolyte. Standard or regarded as optional. 4 Copyright International Organization for Standardization Provided by IHS under license with ISONot for ResaleNo reproduction or networking permitted without license from IHS-,-,-