1、BSI Standards Publication BS ISO 6101-3:2014 Rubber Determination of metal content by atomic absorption spectrometry Part 3: Determination of copper contentBS ISO 6101-3:2014 BRITISH STANDARD National foreword This British Standard is the UK implementation of ISO 6101-3:2014. It supersedes BS 7164-2
2、8.1:1997 which is withdrawn. The UK participation in its preparation was entrusted to Technical Committee PRI/23, Test methods for rubber and non-black compounding ingredients. A list of organizations represented on this committee can be obtained on request to its secretary. This publication does no
3、t purport to include all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2014. Published by BSI Standards Limited 2014 ISBN 978 0 580 82376 3 ICS 83.060 Compliance with a British Standard cannot confer immunity from legal o
4、bligations. This British Standard was published under the authority of the Standards Policy and Strategy Committee on 31 July 2014. Amendments issued since publication Date Text affectedBS ISO 6101-3:2014 ISO 2014 Rubber Determination of metal content by atomic absorption spectrometry Part 3: Determ
5、ination of copper content Caoutchouc Dtermination de la teneur en mtal par spectromtrie dabsorption atomique Partie 3: Dosage du cuivre INTERNATIONAL STANDARD ISO 6101-3 Third edition 2014-08-01 Reference number ISO 6101-3:2014(E)BS ISO 6101-3:2014ISO 6101-3:2014(E)ii ISO 2014 All rights reserved CO
6、PYRIGHT PROTECTED DOCUMENT ISO 2014 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting on the internet or an intranet, without prior written per
7、mission. Permission can be requested from either ISO at the address below or ISOs member body in the country of the requester. ISO copyright office Case postale 56 CH-1211 Geneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749 09 47 E-mail copyrightiso.org Web www.iso.org Published in SwitzerlandBS ISO 61
8、01-3:2014ISO 6101-3:2014(E) ISO 2014 All rights reserved iii Contents Page Foreword iv 1 Scope . 1 2 Normative references 1 3 Principle 1 4 Reagents 2 5 Apparatus . 2 6 Sampling 3 7 Procedure. 3 7.1 Test portion 3 7.2 Preparation of test solution . 4 7.3 Preparation of the calibration graph 4 7.4 De
9、termination . 5 7.5 Blank determination 5 7.6 Number of determinations . 6 8 Expression of results 6 9 Precision . 7 10 Test report . 7 Annex A (informative) Method of standard additions 8 Annex B (informative) Precision 10 Bibliography .11BS ISO 6101-3:2014ISO 6101-3:2014(E) Foreword ISO (the Inter
10、national 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 committee has
11、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 electrotechnical st
12、andardization. The procedures used to develop this document and those intended for its further maintenance are described in the ISO/IEC Directives, Part 1. In particular the different approval criteria needed for the different types of ISO documents should be noted. This document was drafted in acco
13、rdance with the editorial rules of the ISO/IEC Directives, Part 2 (see www.iso.org/directives). 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 identifying any or all such patent rights. Detai
14、ls of any patent rights identified during the development of the document will be in the Introduction and/or on the ISO list of patent declarations received (see www.iso.org/patents). Any trade name used in this document is information given for the convenience of users and does not constitute an en
15、dorsement. For an explanation on the meaning of ISO specific terms and expressions related to conformity assessment, as well as information about ISOs adherence to the WTO principles in the Technical Barriers to Trade (TBT) see the following URL: Foreword - Supplementary information The committee re
16、sponsible for this document is ISO/TC 45, Rubber and rubber products, Subcommittee SC 2, Testing and analysis. This third edition cancels and replaces the second edition (ISO 6101-3:1997), which has been technically revised. ISO 6101 consists of the following parts, under the general title Rubber De
17、termination of metal content by atomic absorption spectrometry: Part 1: Determination of zinc content Part 2: Determination of lead content Part 3 Determination of copper content Part 4: Determination of manganese content Part 5: Determination of iron content Part 6: Determination of magnesium conte
18、ntiv ISO 2014 All rights reservedBS ISO 6101-3:2014INTERNATIONAL ST ANDARD ISO 6101-3:2014(E) Rubber Determination of metal content by atomic absorption spectrometry Part 3: Determination of copper content WARNING Persons using this part of ISO 6101 should be familiar with normal laboratory practice
19、. This part of ISO 6101 does not purport to address all of the safety problems, if any, associated with its use. It is the responsibility of the user to establish appropriate safety and health practices and to ensure compliance with any national regulatory conditions. 1 Scope This part of ISO 6101 s
20、pecifies an atomic absorption spectrometric method for the determination of the copper content of rubbers. The method is applicable to raw rubber and rubber products having copper contents above 1 ppm. Copper contents below this limit can be determined, provided that suitable adjustments are made to
21、 the mass of the test portion and/or to the concentrations of the solutions used. The use of the standard additions method can lower the bottom limit of detection. 2 Normative references The following documents, in whole or in part, are normatively referenced in this document and are indispensable f
22、or its application. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. ISO 123, Rubber latex Sampling ISO 124, Latex, rubber Determination of total solids content ISO 247, Rubber Determinatio
23、n of ash ISO 648, Laboratory glassware Single-volume pipettes ISO 1042, Laboratory glassware One-mark volumetric flasks ISO 1772, Laboratory crucibles in porcelain and silica ISO 1795, Rubber, raw natural and raw synthetic Sampling and further preparative procedures ISO 4793, Laboratory sintered (fr
24、itted) filters Porosity grading, classification and designation 3 Principle A test portion is ashed at 550 C 25 C in accordance with ISO 247, method A. The ash is dissolved in hydrochloric acid or nitric acid. The solution is aspirated into an atomic absorption spectrometer and the absorption is mea
25、sured at a wavelength of 324,7 nm, using a copper hollow-cathode lamp as the copper emission source. Any silicates are volatilized by sulfuric and hydrofluoric acid. NOTE ISO 6955:1982 defines the spectrometric terms used in this part of ISO 6101. ISO 2014 All rights reserved 1BS ISO 6101-3:2014ISO
26、6101-3:2014(E) 4 Reagents During the analysis, unless otherwise stated, use only reagents of recognized analytical grade and only distilled water or water of equivalent purity. 4.1 Hydrochloric acid, 20= 1,18 Mg/m 3 , 37 % (m/m). 4.2 Hydrochloric acid, diluted 1 + 2. Dilute 1 volume of concentrated
27、hydrochloric acid (4.1) with 2 volumes of water. 4.3 Sulfuric acid, 20= 1,84 Mg/m 3 , 95 % (m/m) to 97 % (m/m). 4.4 Sulfuric acid, diluted 1 + 3. Add carefully 1 volume of concentrated sulfuric acid (4.3) to 3 volumes of water. 4.5 Hydrofluoric acid, 20= 1,13 Mg/m 3 , 38 % (m/m) to 40 % (m/m). 4.6 H
28、ydrogen peroxide, 30 % (m/m) solution. 4.7 Concentrated nitric acid, 20= 1,41 Mg/m 3 . 4.8 Dilute nitric acid, 1,6 % (by mass), prepared by carefully pipetting 11,5 cm 3of concentrated nitric acid (4.7) into a 1 000 cm 3one-mark volumetric flask, making up to the mark with water and mixing thoroughl
29、y. 4.9 Standard copper stock solution, containing 1 g of Cu per 1 000 cm 3 . Either use a commercially available standard copper solution, or prepare as follows: Weigh, to the nearest 0,1 mg, 1 g of electrolytic copper (purity 99,9 %) and dissolve in 50 cm 3of concentrated hydrochloric acid (4.1). A
30、dd 15 cm 3of hydrogen peroxide solution (4.6). After dissolution, decompose the excess hydrogen peroxide by boiling. Allow to cool and transfer quantitatively to a 1 000 cm 3one-mark volumetric flask (see 5.5). Dilute to the mark and mix thoroughly. 1 cm 3of this standard stock solution contains 1 0
31、00 g of Cu. 4.10 Standard copper solution, containing 10 mg of Cu per 1 000 cm 3 . Carefully pipet te 10 cm 3of the standard copper stock solution (4.9) into a 1 000 cm 3one-mark volumetric flask (see 5.5) and dilute to the mark with 1 + 2 hydrochloric acid (4.2) or dilute nitric acid (4.8), and mix
32、 thoroughly. Prepare this solution on the day of use. 1 cm 3of this standard stock solution contains 10 g of Cu. 5 Apparatus Ordinary laboratory apparatus, plus the following. 5.1 Atomic absorption spectrometer, fitted with a burner fed with acetylene and air, compressed to at least 60 kPa and 300 k
33、Pa, respectively, and also fitted with a copper hollow-cathode lamp as the copper emission source. The instrument shall be operated in accordance with the manufacturers instructions for optimum performance.2 ISO 2014 All rights reservedBS ISO 6101-3:2014ISO 6101-3:2014(E) Alternatively, an electroth
34、ermal atomization device (graphite furnace) may be used. It shall be operated by a competent person in accordance with the manufacturers instructions for optimum performance. 5.2 Balance, accurate to 0,1 mg. 5.3 Muffle furnace, capable of being maintained at a temperature of 550 C 25 C. 5.4 Glass fi
35、lter crucible, filter pore size 16 m to 40 m (porosity grade P40 according to ISO 4793). 5.5 One-mark volumetric flasks, glass-stoppered, of capacities 50 cm 3 , 100 cm 3 , 200 cm 3 , 500 cm 3and 1 000 cm 3 , complying with the requirements of ISO 1042, class A. 5.6 Volumetric pipettes, of capacitie
36、s 5 cm 3 , 10 cm 3 , 20 cm 3 , and 50 cm 3 , complying with the requirements of ISO 648, class A. 5.7 Graduated pipette, of capacity 1cm 3 , complying with the requirements of ISO 835, class A. 5.8 Electric hotplate, or heated sand bath. 5.9 Steam bath. 5.10 Platinum or borosilicate-glass rod, for u
37、se as a stirrer. 5.11 Crucible, of platinum, and of capacity 50 cm 3to 150 cm 3depending on the test portion size. 5.12 Crucible, of silica, porcelain, or borosilicate glass, of capacity 50 cm 3to 150 cm 3depending on the test portion size, complying with the requirements of ISO 1772. 5.13 Ashless f
38、ilter paper. 6 Sampling Carry out sampling as follows: raw rubber: in accordance with ISO 1795; latex: in accordance with ISO 123; products: to be representative of the whole batch. 7 Procedure 7.1 Test portion Weigh, to the nearest 0,1 mg, approximately 1 g to 5 g of rubber product and 5 g to 10 g
39、of raw rubber, milled or finely cut, into an appropriate crucible. Wrap the test portion in an ashless filter paper and place into an appropriate crucible (5.11 or 5.12). The size of the test portion shall be judged by prior knowledge of the approximate amount of copper present. For natural rubber l
40、atex concentrate, take a portion of thoroughly mixed latex containing about 10 g of total solids, make into a thin film by pouring the portion onto a glass plate, dry to constant mass as specified in ISO 124 and cut into small pieces. For raw, natural rubber, take the test portion from a test sample
41、 prepared in accordance with ISO 1795. ISO 2014 All rights reserved 3BS ISO 6101-3:2014ISO 6101-3:2014(E) 7.2 Preparation of test solution 7.2.1 Destruction of organic matter Ash the test portion in accordance with method A of ISO 247, in the muffle furnace (5.3), maintained at 550 C 25 C. If the as
42、h is black, caused by small amounts of carbon black, stir carefully with the platinum or borosilicate-glass rod (5.10) and continue heating. 7.2.2 Dissolution of inorganic residue using hydrochloric acid After ashing, allow the crucible and its contents to cool to ambient temperature. Add 20 cm 3of
43、concentrated hydrochloric acid (4.1). Heat the mixture on the steam bath (5.9) for at least 10 min. Do not let the reaction mixture boil. Allow to cool to ambient temperature and transfer the solution quantitatively, with the aid of water, to a 50 cm 3one-mark volumetric flask (5.5). If the ash is n
44、ot totally dissolved, proceed as follows. Transfer the solution and the undissolved ash quantitatively, with the aid of water, to a platinum crucible (5.11). Add a few drops of concentrated sulfuric acid (4.3) and 5 cm 3of hydrofluoric acid (4.5). Heat on the electric hotplate or heated sand bath (5
45、.8) in a fume cupboard and evaporate to dryness, while stirring with a platinum rod (5.10). Repeat this digestion with the same quantities of sulfuric and hydrofluoric acids two more times. Allow to cool to ambient temperature, add 20 cm 3of concentrated hydrochloric acid (4.1), heat for 10 min and
46、transfer quantitatively, with the aid of water, to a 50 cm 3one-mark volumetric flask (5.5). Dilute to the mark with water and mix thoroughly. Insoluble matter can settle and, if so, shall be filtered off using a filter crucible (5.4) just before making spectrometric measurements in accordance with
47、7.3. Test solutions should contain approximately 12 % hydrochloric acid. If evaporation, etc., has reduced or increased this concentration, adjust accordingly with concentrated hydrochloric acid (4.1) or water. 7.2.3 Dissolution of inorganic residue using nitric acid Alternative method Add 10 cm 3of
48、 dilute nitric acid (4.8) to the cooled residue. Cover with a watch glass and heat on a steam bath (5.9) for at least 30 min. Allow to cool to ambient temperature. Filter the contents of the crucible into a 50 cm 3one-mark volumetric flask, rinsing the crucible, and making up to the mark with dilute
49、 nitric acid (4.8). 7.3 Preparation of the calibration graph 7.3.1 Preparation of calibration solutions 7.3.1.1 Into a series of five 100 cm 3one-mark volumetric flasks (see 5.5), introduce, using pipettes (see 5.6) the volumes of standard copper solution (4.10) indicated in Table 1. Dilute to the mark with 1 + 2 hydrochloric acid solution (4.2) or dilute nitric acid (4.8) and mix thoroughly. Table 1 Standard calibration solutions Volume of standard copper solution cm 3
