EN ISO 3696-1995 en Water for Analytical Laboratory Use- Specification and Test Methods《分析实验室用水 规范和试验方法(ISO 3696-1987)》.pdf
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1、CEN EN*IS0*3696 95 3404589 0307762 T82 = t - BRITISH STANDARD water for analytical laboratory use - Specification and test methods L The European Standard EN IS0 3696 : 1995 has the status of a British Standard BS EN IS0 3696 : 1995 CEN EN*ISO*3696 95 3404589 0307763 919 M . BS 3978 : 1987 Contents
2、National foreword Committees responsible Specification 1 Scope and field of application 2 Descriqion 3 Classification 4 Requirements Page Inside front cover 5 Sampling Back cover 6 Storage 7 Methods of test 8 Test reports 1 1 Table 1 Requirements 1 Page 2 2 2 5 2 National foreword This British Stand
3、ard has been prepared under the direction of the Chemicals Standards Committee. It is identical with IS0 3696 : 1987 Water for analytical laboratory use - Specification and test methods, published by the International Organization for Standardization (ISO). In- 1995 the European Committee for Standa
4、rdization (CEN) accepted IS0 3696 : 1987 as European Standard EN IS0 3696. As a consequence of implementing the European Standard this British Standard is renumbered as BS EN IS0 3696 and any reference to BS 3978 should be read as a reference to BS EN Is0 3696. This standard IS a rewntc;u IS wiLnara
5、wn. I he principal changes ;-.this edition.are as tiiows. (a) The single grade of water has been replaced by three grades, of which grade 3 is roughly Equivalent to the water specified in the previous edition. (b) Residue on ignition is no longer specified and the requirement (for grade 3 water) for
6、 residue on evaporation has been tightened. (c) Electrical conductivity is now measured at 25 “C instead of 20 OC, and the requirement for grade 3 water has been changed from 1 mS/m to 0.5 mS/m. (d) The limit for oxidizable matter for grade 3 water has been tightened. (e) Requirements for ammonia co
7、ntent, chloride content and sulphate content are no longer included. 99.9 % of Cio7), previously dried at 110 OC, into the 7.6.2.2 Matched Nessler cylinders, of capacity 50 ml. platinum dish (7.5.2.3)- dd 4,s g of sodium carbonate * (anhydrous Na,CO,) and intimately mix the sample with a dry, smooth
8、-ended glass rod. Ease the mixture into the centre of the dish and flatten it so that it covers an area 0.5 g of the sodium carbonate, then gently brush any 7.6.2.3 Muffle 4oo oc. capable of being at 3oo to 30 mm in diameter. cover the mixture with a further 7.6.2.4 Water-bath. capable of being Cont
9、rolled at approx- imately 60 OC. particles adhering to the glass rod into the dish. Cover the dish with a platinum lid and place in the muffle fur- nace (7.6.2.31. controlled at 300 to 400 OC. Heat the mixture, gradually raising the temperature for about 10 min or until fusion is complete. Remove th
10、e dish from the furnace and gently swirl it to incorporate any particles. Allow to cool, wash into the dish any particles adhering to the underside of the lid with hot water, then dissolve the fused mass in hot water. Cool, transfer the solution quantitatively to a 1 o00 ml one- mark volumetric flas
11、k, dilute to the mark and mix. Transfer the solution to the plastics bottle for storage. 1 ml of this standard solution contains 1 mg of 50,. 7.6.3 Procedure 7.6.3.1 Test portion Take 520 ml of grade 1 water or 270 ml of grade 2 water. 7.6.3.2 Test Evaporate the test portion (7.6.3.1 1 in the dish (
12、7.6.2.1) in suc- cessive portions, to produce a final volume of 20 ml. Add 1 ml of the ammonium molybdate solution (7.6.1.31. After exactly 5 min, add 1 ml of the oxalic acid solution (7.6.1.6) and mix well. After 1 min, add 1 ml of the metol solution (7.6.1.41, and See national foreword for details
13、 of textual errors. 4 CEN EN*IS0*3696 95 = 3404589 0307770 059 BS 3978 : 1987 heat for 10 min in the water bath (7.6241, maintained at ap- proximately 60 OC. Transfer the solution to one of the matched Nessler cylinders (7.6.2.2). Prepare a standard colour solution following the same pro- cedure, bu
14、t using a mixture of 19.0 ml of the sample and 1.0 rnl of the standard silica solution (7.6.1.2) instead of the 20 ml resulting from the evaporation of the test portion (7.6.3.1 ). Transfep the solution to the other matched Nessler cylinder (7.6.2.2). kS, Viewing vertically downwards, check that the
15、 intensity of any blue colour produced in the test solution does not exceed that produced in the standard colour solution 8 Test reports Each test report shall include the following particulars : al an identification of the sample; b) the reference of the method used: e) the results and the methad b
16、f expression used; di any unusual features noted during the determination; e) dard, or regarded as optional. any operation not included in this International Stan- 5 CEN EN*IS0*3bb 95 = 3404569 0107771 T95 Amd. No. -? - This British Standard, having been prepared under the direction of the Chemicals
17、 Standards Committee, was published under the authority of the Board of BSI and comes into effect on 31 December 1987. O British Standards Institution, 1987 First published February 1966 First revisioryDecember 1987 ISBN O 580 16312 1 The following BSI references relate to the work on this standard:
18、 Committee reference CIC/26 Draft for comment 83/55146 DC Date of issue 3 E? +I- 1-5- 9 .- 4 British Standards Institution. Incorporated by Royal Charter, BSI is the independent national body for the preparation of British Standards. It is the UK member of the International Organization for Standard
19、ization and UK sponsor of the British National Committee of the International Electrotechnical Commission. In addition to the preparation and promulgation of standards, BSI offers specialist services including the provision of information through the BSI Library and Standardline Database; Technical
20、Help to Exporters; and other services. Advice can be obtained from the Enquiry Section, BSI, Milton Keynes MK14 6LE. telephone 0908 221 166, telex 825777. Copyright. Users of British Standards are reminded that copyright subsists in ali BSI publications. No part of this publication may be reproduced
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