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1、 Reference number ISO 24538:2008(E) ISO 2008 INTERNATIONAL STANDARD ISO 24538 First edition 2008-11-01 Plastics Homopolymer and copolymer resins of vinyl chloride Determination of residual vinyl chloride monomer by gas-chromatographic analysis of dry powder Plastiques Rsines dhomopolymres et de copo
2、lymres de chlorure de vinyle Dosage du chlorure de vinyle rsiduel par chromatographie en phase gazeuse sur poudre sche Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/5910770001 Not for Resale, 01/29/2009 23:41:31 MSTNo reproduction
3、or networking permitted without license from IHS -,-,- ISO 24538:2008(E) PDF disclaimer This PDF file may contain embedded typefaces. In accordance with Adobes licensing policy, this file may be printed or viewed but shall not be edited unless the typefaces which are embedded are licensed to and ins
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6、 please inform the Central Secretariat at the address given below. COPYRIGHT PROTECTED DOCUMENT ISO 2008 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying and microf
7、ilm, without permission in writing 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 Switzerland ii ISO 200
8、8 All rights reserved Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/5910770001 Not for Resale, 01/29/2009 23:41:31 MSTNo reproduction or networking permitted without license from IHS -,-,- ISO 24538:2008(E) ISO 2008 All rights rese
9、rved iii Contents Page Foreword iv 1 Scope . 1 2 Normative references. 1 3 Terms and definitions. 1 4 Principle. 1 5 Apparatus and materials 2 6 Sampling 2 7 Procedure 2 8 Procedure A. 3 8.1 Preparation of test sample and analysis 3 8.2 Calibration . 3 8.3 Calculation. 3 9 Procedure B. 5 9.1 Prepara
10、tion of test sample and analysis 5 9.2 Calibration . 5 9.3 Calculation. 6 10 Precision 7 11 Test report . 7 Annex A (informative) Examples of suitable columns . 8 Bibliography. 9 Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/591077
11、0001 Not for Resale, 01/29/2009 23:41:31 MSTNo reproduction or networking permitted without license from IHS -,-,- ISO 24538:2008(E) iv ISO 2008 All rights reserved Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bo
12、dies). 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 been established has the right to be represented on that committee. International organizations, governmental an
13、d 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 standardization. International Standards are drafted in accordance with the rules given in the ISO/IEC Directives,
14、 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 member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies cas
15、ting 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 identifying any or all such patent rights. ISO 24538 was prepared by Technical Committee ISO/TC 61, Plastics, Subcommittee SC 5, Ph
16、ysical- chemical properties. Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/5910770001 Not for Resale, 01/29/2009 23:41:31 MSTNo reproduction or networking permitted without license from IHS -,-,- INTERNATIONAL STANDARD ISO 24538:20
17、08(E) ISO 2008 All rights reserved 1 Plastics Homopolymer and copolymer resins of vinyl chloride Determination of residual vinyl chloride monomer by gas-chromatographic analysis of dry powder SAFETY STATEMENT Persons using this document should be familiar with normal laboratory practice, if applicab
18、le. This document does not purport to address all of the safety concerns, 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 regulatory requirements. 1 Scope This International Standard specifie
19、s a method for the determination of residual vinyl chloride monomer in homopolymer and copolymer resins of vinyl chloride. The method is based on a static headspace gas-chromatographic technique (i.e. the analysis of the vapour phase in equilibrium with the solid phase at constant temperature) and i
20、s suitable for all kinds of homopolymer and copolymer resin. It is done directly on the resin in powder form. For compounded material, granulate, extrudate, films, etc., use ISO 6401. NOTE In the case of compounded material, it is necessary to dissolve the sample in a suitable solvent in order to re
21、ach complete headspace equilibrium. 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 amendments)
22、 applies. ISO 472, Plastics Vocabulary 3 Terms and definitions For the purposes of this document, the terms and definitions given in ISO 472 apply. 4 Principle A weighed amount of the sample is sealed into a glass vial. After thermal conditioning for a certain period of time to permit the vinyl chlo
23、ride monomer (VCM) to equilibrate between the powder and the vapour phase, a gas sample is taken from the headspace, e.g. by automatic injection, into the gas chromatograph. The components are separated on a column and detected using a flame-ionization detector. Copyright International Organization
24、for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/5910770001 Not for Resale, 01/29/2009 23:41:31 MSTNo reproduction or networking permitted without license from IHS -,-,- ISO 24538:2008(E) 2 ISO 2008 All rights reserved 5 Apparatus and materials 5.1 Gas chromatograph, fit
25、ted either with an automatic static headspace sampler or with facilities for manual sample injection. Chromatographic columns and conditions shall be chosen in such a way that VCM and impurities are separated reliably. NOTE Examples of suitable columns are described in Annex A. 5.2 Flame-ionization
26、detector (FID). 5.3 Glass vials, for most purposes of capacity 22 ml and 10 ml, with PTFE-faced silicone or butyl rubber septa and aluminium caps. No peaks which could interfere with the VCM determination shall come from the septa. 5.4 Crimping and decapping tools, for sealing and reopening the vial
27、s. 5.5 Gastight syringes, of capacity up to 5 ml, depending on the VCM concentration. Syringes are chosen in accordance with the volume analysed. 5.6 Analytical balance, capable of reading to 0,1 mg. 5.7 Data system, or equivalent system (recording potentiometer or integrator), for the acquisition a
28、nd evaluation of gas-chromatographic data. 5.8 Vinyl chloride gas standards, prepared by consecutive dilution of pure VCM (purity greater than 99,5 % by volume), for calibration purposes. The use of a commercially available standard in helium, nitrogen or air in a gas cylinder fitted with a capillar
29、y outlet or a syringe adapter is recommended. SAFETY PRECAUTIONS Vinyl chloride is a flammable gas at ambient temperature. The preparation of calibration samples must therefore be carried out under a well-ventilated hood. 5.9 FID gases and carrier gas. For low limits of quantification, so-called “ze
30、ro air” (dry, contaminant-free air) shall be used for the FID and the other gases used shall be of similarly high purity. 6 Sampling During storage, a concentration gradient may have formed in the PVC being sampled, since the upper layers release residual VCM faster. Cooling of the sample is advisab
31、le, but condensation of humidity shall be avoided. To minimize losses of residual monomer, carry out sample preparation as quickly as possible. When exchanging samples between laboratories or when storage is necessary, seal samples in completely filled glass vials. 7 Procedure Two different procedur
32、es are described. Procedure A is suitable for determining the residual VCM content of homopolymers and copolymers of vinyl chloride down to a level of 0,01 mg/kg. Calibration is performed by adding known amounts of VCM to samples of completely VCM-free PVC. Procedure B is similar to procedure A exce
33、pt that a smaller amount of test sample is used and calibration is performed using external VCM standards rather than VCM added to PVC. Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/5910770001 Not for Resale, 01/29/2009 23:41:31 MS
34、TNo reproduction or networking permitted without license from IHS -,-,- ISO 24538:2008(E) ISO 2008 All rights reserved 3 In procedure A, it is important to perform the calibration using the same type of PVC as that being analysed and using the same mass of PVC as that taken as the test sample. It is
35、 also important that equilibrium between the solid and gaseous phases be established under the same conditions during calibration and during actual analysis and that the reduction in the headspace volume caused by the presence of the PVC in the vial be allowed for. 8 Procedure A 8.1 Preparation of t
36、est sample and analysis Before taking the test sample, it is recommended that the vial into which the test sample will be placed be purged with nitrogen in order to remove any possible traces of VCM. Weigh between 2 g and 4 g of the PVC resin to be analysed (the same amount as used for calibration),
37、 to the nearest 0,001 g, into a clean 22 ml vial and seal the vial immediately with a septum and an aluminium cap. Place it in the headspace sampler of the gas chromatograph for 15 min at 120 C to allow it to come to temperature equilibrium and then start the analysis run. Perform two determinations
38、 on each sample. 8.2 Calibration Calibration is performed by adding known amounts of VCM to samples of totally degassed (i.e. VCM-free) PVC in vials. In order to ensure that the same equilibrium is established between the solid and gaseous phases during calibration as during the actual analysis and
39、in order to allow for the reduction in headspace volume caused by the presence of the PVC in the vial, use the same mass (for example 2 g) and the same type of PVC for the calibration as for the actual analysis. NOTE The mass of PVC taken to prepare the calibration standards and the test sample will
40、 affect the sensitivity of the method. To obtain VCM-free PVC, heat the PVC in an oven at 100 C until the VCM peak given by the degassed PVC is no longer detectable by the chromatograph. The calibration can be performed using diluted or pure VCM gas. Take five 22 ml headspace vials, each containing
41、between 2 g and 4 g of VCM-free PVC resin weighed to the nearest 0,001 g. If diluted (for example 0,4 %) VCM gas is used to prepare these calibration standards, transfer, for instance, 0 ml, 0,2 ml, 0,5 ml, 1 ml and 2 ml of the VCM gas to the individual vials using gastight syringes. If pure VCM gas
42、 is used, transfer, for instance, 0 l, 2,5 l, 5 l, 10 l and 20 l of the VCM gas to the individual vials, again using gastight syringes. Allow the vials to stand at room temperature for at least half an hour to allow the VCM to equilibrate between the headspace and the PVC. Then place the vials conta
43、ining the calibration standards in the static headspace sampler (or in a thermostatic bath) and allow to come to temperature equilibrium at 120 C for 15 min before analysis. Keep all parameters (time allowed for the vial and contents to come to temperature equilibrium, the equilibrium temperature, t
44、he injection parameters, etc.) constant for calibration and sample analysis. 8.3 Calculation 8.3.1 General Carry out the calculations below to one decimal place. Copyright International Organization for Standardization Provided by IHS under license with ISO Licensee=Boeing Co/5910770001 Not for Resa
45、le, 01/29/2009 23:41:31 MSTNo reproduction or networking permitted without license from IHS -,-,- ISO 24538:2008(E) 4 ISO 2008 All rights reserved 8.3.2 Evaluation of the calibration run The calculation of the results can be done by evaluation of the peak area. 8.3.3 Calculation of the mass of VCM c
46、alibration standard in each vial When commercially available diluted VCM gas in a gas cylinder is used for calibration, the concentration of the VCM gas may be given in millilitres per cubic metre. If so, it is first necessary to convert this to milligrams per cubic metre, as follows: /VCM / v v w v
47、 cM c V = where cw/v is the concentration of the VCM gas in the gas cylinder in milligrams per cubic metre (mg/m3); cv/v is the concentration of the VCM gas in the gas cylinder in millilitres per cubic metre (ml/m3); MVCM is the molar mass of VCM (= 62,5 g); V is the molar volume at 20 C and 1 013 m
48、bar (= 24,1 l). Then calculate the mass of VCM in each vial using the following equation: /D St 1000 w v cV c = where cSt is the mass of VCM in the vial, in milligrams (mg); cw/v is the concentration of the VCM gas in the gas cylinder in milligrams per cubic metre (mg/m3); VD is the volume of VCM gas introduced into the vial, in litres (l). If the calibration is performed using pure VCM, cSt is calculated using the same equations, but using a value for cv/v of 1. In order to take into account the (non-negligibl