1、 Collection of SANS standards in electronic format (PDF) 1. Copyright This standard is available to staff members of companies that have subscribed to the complete collection of SANS standards in accordance with a formal copyright agreement. This document may reside on a CENTRAL FILE SERVER or INTRA
2、NET SYSTEM only. Unless specific permission has been granted, this document MAY NOT be sent or given to staff members from other companies or organizations. Doing so would constitute a VIOLATION of SABS copyright rules. 2. Indemnity The South African Bureau of Standards accepts no liability for any
3、damage whatsoever than may result from the use of this material or the information contain therein, irrespective of the cause and quantum thereof. ISBN 978-0-626-19575-5 SANS 3071:2007Edition 1ISO 3071:2005Edition 3SOUTH AFRICAN NATIONAL STANDARD Textiles Determination of pH of aqueous extract This
4、national standard is the identical implementation of ISO 3071:2005 and is adopted with the permission of the International Organization for Standardization. Published by Standards South Africa 1 dr lategan road groenkloof private bag x191 pretoria 0001 tel: 012 428 7911 fax: 012 344 1568 internation
5、al code + 27 12 www.stansa.co.za Standards South Africa SANS 3071:2007 Edition 1 ISO 3071:2005 Edition 3 Table of changes Change No. Date Scope National foreword This South African standard was approved by National Committee StanSA SC 5110.04C, Textile test methods Chemical analysis, in accordance w
6、ith procedures of Standards South Africa, in compliance with annex 3 of the WTO/TBT agreement. This standard was published in March 2007. This SANS edition cancels and replaces SANS 51413:2003/EN1413:1998. Reference numberISO 3071:2005(E)ISO 2005INTERNATIONAL STANDARD ISO3071Third edition2005-06-15T
7、extiles Determination of pH of aqueous extract Textiles Dtermination du pH de lextrait aqueux SANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .ISO 3071:2005(E) PDF disclaimer This PDF file may contain embedded typefaces. In accor
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12、eneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749 09 47 E-mail copyrightiso.org Web www.iso.org Published in Switzerland ii ISO 2005 All rights reservedSANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .ISO 3071:2005(E) ISO 2005 All
13、rights reserved iiiContents Page Foreword iv Introduction v 1 Scope . 1 2 Normative references . 1 3 Terms and definitions. 1 4 Principle. 1 5 Reagents 1 6 Apparatus 2 7 Preparation of test samples. 2 8 Procedure 2 8.1 Preparation of the aqueous extract 2 8.2 Measurement of the pH of the aqueous ext
14、ract 2 9 Calculation. 3 10 Precision 3 11 Test report . 3 Annex A (informative) Preparation of standard buffer solutions 4 SANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .ISO 3071:2005(E) iv ISO 2005 All rights reservedForeword
15、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 subject for which a technical
16、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 (IEC) on all matters of elect
17、rotechnical standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2. The main task of technical committees is to prepare International Standards. Draft International Standards adopted by the technical committees are circulated to the
18、member bodies for voting. Publication 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 document may be the subject of patent rights. ISO shall not be held responsible for ident
19、ifying any or all such patent rights. ISO 3071 was prepared by Technical Committee ISO/TC 38, Textiles. This third edition cancels and replaces the second edition (ISO 3071:1980), which has been technically revised. SANS 3071:2007This s tandard may only be used and printed by approved subscription a
20、nd freemailing clients of the SABS .ISO 3071:2005(E) ISO 2005 All rights reserved vIntroduction The pH-value of the aqueous extract of a textile affords a useful index to its processing history. In addition, it is becoming more common to demand that the textile, in its various forms, conforms to cer
21、tain limits in respect of its acidity or alkalinity, often expressed in terms of the pH-value of the aqueous extract. SANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .SANS 3071:2007This s tandard may only be used and printed by a
22、pproved subscription and freemailing clients of the SABS .INTERNATIONAL STANDARD ISO 3071:2005(E) ISO 2005 All rights reserved 1Textiles Determination of pH of aqueous extract 1 Scope This International Standard specifies a method for determining the pH of the aqueous extract of textiles. The method
23、 is applicable to textiles in any form. 2 Normative references The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendme
24、nts) applies. ISO 3696:1987, Water for analytical laboratory use Specification and test methods 3 Terms and definitions For the purposes of this document, the following terms and definitions apply. 3.1 pH co-logarithm of the hydrogen ion concentration in an aqueous extract 4 Principle The pH-value o
25、f an aqueous extract of a textile is measured electrometrically at room temperature by means of a glass electrode. 5 Reagents All reagents used shall be of recognized analytical grade. 5.1 Distilled or deionized water, of at least grade 3 as defined in ISO 3696, having a pH between 5,0 and 7,5. The
26、pH shall be verified the first time the water is used. If it is not within the specified range, the water shall be redistilled using chemically resistant glassware. Acid or organic matter can be removed by distilling water from a solution of 1 g/l potassium permanganate and 4 g/l sodium hydroxide. A
27、lkalinity (e.g. the presence of ammonia) can be removed by distilling the water from a solution of dilute sulfuric acid. If the distilled water is not grade 3, boil 100 ml of distilled water in a beaker at a moderate rate for (10 1) min and allow the covered beaker to cool to room temperature. 5.2 P
28、otassium chloride solution, 0,1 mol/l, prepared using distilled or deionized water (5.1). 5.3 Buffer solutions, which may be prepared as specified in Annex A, having a pH similar to that being determined, for calibration of the pH-meter before measurement. Buffer solutions having a pH around 4, 7 or
29、 9 are recommended. SANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .ISO 3071:2005(E) 2 ISO 2005 All rights reserved6 Apparatus 6.1 Stoppered glass or polypropylene flasks, chemically resistant, for preparation of the aqueous ext
30、ract. NOTE It is recommended that the glassware used for this test be set aside for this purpose only and filled with distilled water between tests. 6.2 Mechanical shaker, providing rotational or reciprocating movement sufficient to obtain a ready exchange of liquid between the interior of the texti
31、le material and the solution used in preparing the extract. A to-and-fro movement at a rate of 60 min1or a rotational frequency of 30 min1has been found satisfactory. 6.3 Beakers, chemically resistant, with a capacity of 150 ml (see Note to 6.1). 6.4 Rods, chemically resistant (see Note to 6.1). 6.5
32、 pH-meter, with a glass electrode, capable of measuring to at least 0,1 pH-units. 6.6 Balance, accurate to 0,01 g. 6.7 1 l volumetric flasks, of grade A quality. 7 Preparation of test samples 7.1 Take a laboratory sample representative of the bulk of the textile material and sufficient to provide al
33、l the test samples required. Cut the laboratory sample into pieces having approximately 5 mm sides or of such a size as to allow the test samples to wet out rapidly. 7.2 To avoid contamination, handle the material as little as possible. Take from the laboratory sample three test samples of (2,00 0,0
34、5) g each. 8 Procedure 8.1 Preparation of the aqueous extract Prepare the extract in triplicate at room temperature, as follows: Place each test sample and 100 ml of extracting solution either water (5.1) or potassium chloride solution (5.2) into a stoppered flask (6.1). Agitate the flask for a shor
35、t period by hand to ensure that the textile material is properly wetted out, then shake it mechanically for 2 h 5 min. Record the temperature of the extracting solution used. 8.2 Measurement of the pH of the aqueous extract Calibrate the pH-meter at the temperature of the extract to be measured. Che
36、ck the calibration of the pH-meter using two buffer solutions. Immerse the electrode several times in the same solution (water or KCl solution) used to prepare the extract until the indicated pH-value stabilizes. Decant the first extract into a beaker, immediately immerse the electrode to a depth of
37、 at least 10 mm and stir gently with a rod until the pH-value stabilizes (do not record the pH-value of this solution). Decant the second extract into another beaker, immediately immerse the electrode, without washing, in the beaker to a depth of at least 10 mm and allow to stand without stirring un
38、til the pH-value stabilizes. Record this value. SANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .ISO 3071:2005(E) ISO 2005 All rights reserved 3Decant the third extract into another beaker, immediately immerse the electrode, with
39、out washing, in the beaker to a depth of at least 10 mm and allow to stand without stirring until the pH-value stabilizes. Record this value. Record the pH-values of the second and third extracts as the first and second measurements. 9 Calculation If the difference between the two pH-values, express
40、ed to the nearest 0,1 pH-units, is greater than 0,2, repeat the procedure with other test samples. When two valid measurements have been obtained, calculate the mean value. 10 Precision Interlaboratory trials were carried out between nine laboratories measuring seven samples. Statistical analysis wa
41、s carried out and the following results were obtained: Using water (5.1) as the extracting solution: Reproducibility limit R = 1,7 pH-units; Using KCl solution (5.2) as the extracting solution: Reproducibility limit R = 1,1 pH-units. NOTE The statistical analysis was carried out in accordance with I
42、SO 5725-2, Accuracy (trueness and precision) of measurement methods and results Part 2: Basic method for the determination of repeatability and reproducibility of a standard measurement method. 11 Test report The test report shall include the following information: a) a reference to this Internation
43、al Standard, i.e. ISO 3071; b) the mean pH-value, to the nearest 0,1 pH-units; c) the type of solution used (water or KCl solution); d) the pH of the extracting solution; e) the temperature of the extracting solution; f) any factor likely to have had an effect on the results, including any resistanc
44、e to wetting out of the test samples g) the date of the determination. SANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .ISO 3071:2005(E) 4 ISO 2005 All rights reservedAnnex A (informative) Preparation of standard buffer solutions
45、 A.1 General Use only reagents of recognized analytical reagent grade. Prepare the buffer solutions using water of at least grade 3 as defined in ISO 3696 and renew them at least once a month. A.2 pH 4,0 potassium hydrogen phthalate solution (0,05 mol/l) Dissolve 10,21 g of potassium hydrogen phthal
46、ate (KHC8H4O4) in distilled or deionized water in a 1 l volumetric flask and dilute to the mark. The pH of this solution is 4,00 at 20 C and 4,01 at 25 C. A.3 pH 6,9 potassium dihydrogen orthophosphate and disodium hydrogen orthophosphate solution (0,08 mol/l) Dissolve 3,9 g of potassium dihydrogen
47、orthophosphate (KH2PO4) and 3,54 g of disodium hydrogen orthophosphate (Na2HPO4) in distilled or deionized water in a 1 l volumetric flask and dilute to the mark. The pH of this solution is 6,87 at 20 C and 6,86 at 25 C. A.4 pH 9,2 disodium tetraborate solution (0,01 mol/l) Dissolve 3,80 g of disodi
48、um tetraborate decahydrate (Na2B40710H2O) in distilled or deionized water in a 1 l volumetric flask and dilute to the mark. The pH of this solution is 9,23 at 20 C and 9,18 at 25 C. Standards South AfricaSANS 3071:2007This s tandard may only be used and printed by approved subscription and freemailing clients of the SABS .
