BS ISO 10315-2013 Cigarettes Determination of nicotine in smoke condensates Gas-chromatographic method《香烟 烟雾冷凝物中尼古丁的测定 气相色谱测定方法》.pdf

《BS ISO 10315-2013 Cigarettes Determination of nicotine in smoke condensates Gas-chromatographic method《香烟 烟雾冷凝物中尼古丁的测定 气相色谱测定方法》.pdf》由会员分享，可在线阅读，更多相关《BS ISO 10315-2013 Cigarettes Determination of nicotine in smoke condensates Gas-chromatographic method《香烟 烟雾冷凝物中尼古丁的测定 气相色谱测定方法》.pdf（18页珍藏版）》请在麦多课文档分享上搜索。

1、BSI Standards PublicationBS ISO 10315:2013Cigarettes Determination of nicotine in smoke condensates Gas-chromatographic methodIncorporating corrigendum September 2015BS ISO 10315:2013 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of ISO 10315:2013. It supersedes BS

2、ISO 10315:2000+A1:2011 which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee AW/40, Tobacco and tobacco products.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include al

3、l the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2015.Published by BSI Standards Limited 2015 ISBN 978 0 580 91495 9 ICS 65.160 Compliance with a British Standard cannot confer immunity from legal obligations.This British

4、Standard was published under the authority of the Standards Policy and Strategy Committee on 31 March 2013. Amendments/corrigenda issued since publicationDate Text affectedImplementation of ISO corrected text: wording of 31 September 20154.2 clarified ISO 2013Cigarettes Determination of nicotine in

5、smoke condensates Gas-chromatographic methodCigarettes Dosage de la nicotine dans les condensats de fume Mthode par chromatographie en phase gazeuseINTERNATIONAL STANDARDISO10315Third edition2013-03-01Reference numberISO 10315:2013(E)Corrected version2014-11-01ISO 10315:2013(E)ii ISO 2013 All rights

6、 reservedCOPYRIGHT PROTECTED DOCUMENT ISO 2013All 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 w

7、ritten permission. Permission can be requested from either ISO at the address below or ISOs member body in the country of the requester.ISO copyright officeCase postale 56 CH-1211 Geneva 20Tel. + 41 22 749 01 11Fax + 41 22 749 09 47E-mail copyrightiso.orgWeb www.iso.orgPublished in SwitzerlandBS ISO

8、 10315:2013ISO 10315:2013(E)Contents PageForeword ivIntroduction v1 Scope . 12 Normative references 13 Principle 14 Reagents 15 Apparatus . 26 Procedure. 26.1 Test portion 26.2 Setting up the apparatus. 36.3 Calibration of the gas chromatograph 36.4 Determination . 37 Expression of results 38 Repeat

9、ability and reproducibility 39 Alternative gas-chromatographic procedures and analysis precautions 49.1 General . 49.2 Alternative columns 49.3 Injection systems 59.4 Alternative internal standards 510 Test report . 5Annex A (informative) Use of this method with the gas-chromatographic determination

10、 of water 6Bibliography 7 ISO 2013 All rights reserved iiiBS ISO 10315:2013ISO 10315:2013(E)ForewordISO (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 o

11、ut 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 and non-governmental, in liaison with ISO, also take part in the work. ISO c

12、ollaborates 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, Part 2.The main task of technical committees is to prepare International S

13、tandards. 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 casting a vote.Attention is drawn to the possibility that some of the elements

14、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 10315 was prepared by Technical Committee ISO/TC 126, Tobacco and tobacco products.This third edition cancels and replaces the second edition (ISO 10315:2000), wh

15、ich has been technically revised. It also incorporates the Amendment ISO 10315:2000/Amd 1:2011 and the Technical Corrigendum ISO 10315:2000/Cor 1:2000.This corrected version of ISO 10315:2013 incorporates the following correction: the wording of 4.2 has been clarified.iv ISO 2013 All rights reserved

16、BS ISO 10315:2013ISO 10315:2013(E)IntroductionThis International Standard may be considered as part of a set produced by ISO/TC 126 which describes the determination of total and nicotine-free dry particulate matter (NFDPM) in cigarette smoke condensates. The set comprises:ISO 3308, ISO 3402, ISO 43

17、87, ISO 8243, ISO 10315, and ISO 10362-1.A related International Standard, ISO 3400, determines total alkaloids, whereas this International Standard determines only nicotine by virtue of the gas-chromatographic separation. Occasionally, differences can occur because of minor amounts of alkaloids oth

18、er than nicotine in some types of tobacco.Annex A provides information about the use of this method in conjunction with or simultaneously with the gas-chromatographic method of water determination specified in ISO 10362-1.A bibliography is provided.No machine smoking regime can represent all human s

19、moking behaviour: it is recommended that cigarettes also be tested under conditions of a different intensity of machine smoking than those specified in this International Standard; machine smoking testing is useful to characterize cigarette emissions for design and regulatory purposes, but communica

20、tion of machine measurements to smokers can result in misunderstandings about differences in exposure and risk across brands; smoke emission data from machine measurements may be used as inputs for product hazard assessment, but they are not intended to be nor are they valid as measures of human exp

21、osure or risks. Communicating differences between products in machine measurements as differences in exposure or risk is a misuse of testing using ISO standards. ISO 2013 All rights reserved vBS ISO 10315:2013Cigarettes Determination of nicotine in smoke condensates Gas-chromatographic methodWARNING

22、 The use of this International Standard can involve hazardous materials, operations, and equipment. This International Standard does not purport to address all the safety problems associated with its use. It is the responsibility of the user of this International Standard to establish appropriate sa

23、fety and health practices and determine the applicability of regulatory limitations prior to use.1 ScopeThis International Standard specifies a method for the gas-chromatographic determination of nicotine in cigarette smoke condensates. The smoking of cigarettes and the collection of mainstream smok

24、e are normally carried out in accordance with ISO 4387.NOTE 1 The method specified in this International Standard is also applicable to the determination of nicotine in cigarette smoke condensates obtained by non-standard smoking.NOTE 2 In countries not in a position to use the gas-chromatographic m

25、ethod, reference should be made to ISO 3400 for the determination of total nicotine alkaloids. In such cases, values obtained using the method described in ISO 3400 may be used with the addition of a note in the expression of results.2 Normative referencesThe following documents, in whole or in part

26、, are normatively referenced in this document and are indispensable for 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 4387, Cigarettes Determination of total and nico

27、tine-free dry particulate matter using a routine analytical smoking machine3 PrincipleThe smoke condensate from the mainstream smoke is dissolved in a solvent containing an internal standard. The nicotine content of an aliquot of the solution is determined by gas chromatography, and the nicotine con

28、tent of the whole of the smoke condensate is calculated.4 ReagentsUse only reagents of recognized analytical reagent grade.4.1 Carrier gas: helium (CAS: 7440-59-7) or nitrogen (CAS: 7727-37-9) of high purity (at least 99,999 %).4.2 Auxiliary gases: hydrogen (CAS: 1333-74-0) of high purity (at least

29、99,999 %) and air for the flame ionization detector.4.3 Propan-2-ol (CAS: 67-63-0), with maximum water content of 1,0 mg/ml.INTERNATIONAL STANDARD ISO 10315:2013(E) ISO 2013 All rights reserved 1BS ISO 10315:2013ISO 10315:2013(E)4.4 Internal standard: n-heptadecane (CAS: 629-78-7) or quinaldine (CAS

30、: 91-63-4) of purity not less than 99 %.Carvone (CAS: 99-49-0), n-octadecane (CAS: 593-45-3), or other appropriate internal standards may be used after assessment of their purity and determination that the internal standard does not co-elute with other components in the smoke extract. The peak area

31、of the internal standard on samples should be monitored for consistency. In cases where inconsistencies are found, analysis of an extraction of a smoke sample without the internal standard in the extraction solution should be performed to confirm the absence of a peak in the smoke extract eluting at

32、 the same time as the internal standard (see Clause 9).4.5 Extraction solvent: propan-2-ol (4.3) containing an appropriate concentration of internal standard (4.4); this is normally in the range of 0,2 mg/ml to 0,5 mg/ml.Solvent not stored in a temperature-controlled laboratory shall be allowed to e

33、quilibrate to (22 2) C before use.4.6 Reference substance: nicotine (CAS: 54-11-5) of known purity not less than 98 %.Store this at between 0 C and 4 C and exclude light.Nicotine salicylate (CAS: 29790-52-1) of known purity not less than 98 % may also be used.NOTE The purity of the nicotine or nicot

34、ine salicylate may be verified in accordance with ISO 13276 or by any other validated method.4.7 Calibration solutionsDissolve the nicotine (4.6) in the solvent (4.5) to produce a series of at least four calibration solutions with concentrations that cover the range expected to be found in the test

35、portion (usually 0,02 mg/ml to 2,0 mg/ml). Store these solutions at between 0 C and 4 C and exclude light.Solvent and solutions stored at low temperatures shall be allowed to equilibrate to (22 2) C before use.5 ApparatusUsual laboratory apparatus and, in particular, the following items.5.1 Gas-chro

36、matograph, equipped with a flame ionization detector, recorder, and integrator or other suitable data handling instrument (see Clause 9).5.2 Column, of internal diameter between 2 mm and 4 mm and preferably of length 1,5 m to 2 m.The column is preferably made of glass, but other materials such as de

37、activated stainless steel or nickel may be used. Stationary phase: 10 % poly(ethylene glycol) (PEG) 20 000 plus 2 % potassium hydroxide on an acid-washed silanized support material, 150 m (100 mesh) to 190 m (80 mesh) (see also Clause 9).6 Procedure6.1 Test portionPrepare the test portion by dissolv

38、ing the smoke condensate obtained by the machine smoking of a known number of cigarettes in a fixed volume of the solvent (4.5) of 20 ml for 44 mm discs, or 50 ml for 92 mm discs, ensuring that the disc is fully covered. The volume may be adjusted to give a concentration of nicotine appropriate for

39、the calibration graph (see 6.3) provided that there is adequate volume for effective extraction of the smoke condensate. Analysis should be performed as soon as possible, but if storage is inevitable then store the sample at between 0 C and 4 C and exclude light. For standard smoking, refer to ISO 4

40、387.2 ISO 2013 All rights reservedBS ISO 10315:2013ISO 10315:2013(E)6.2 Setting up the apparatusSet up the apparatus and operate the gas chromatograph (5.1) in accordance with the manufacturers instructions. Ensure that the peaks for solvent, internal standard, nicotine, and other smoke component pe

41、aks, especially neophytadiene (which can appear on the tail of the nicotine peak under certain circumstances), are well resolved (see also Clause 9).Suitable operating conditions are as follows: column temperature, 170 C (isothermal); injection temperature, 250 C; detector temperature, 250 C; carrie

42、r gas, helium, or nitrogen at a flow rate of about 30 ml/min; injection volume, 2 l.Using the above conditions, the analysis time is about 6 min to 8 min (see also Clause 9).6.3 Calibration of the gas chromatographInject an aliquot (2 l) of each of the calibration solutions (4.7) into the gas chroma

43、tograph. Record the peak areas (or heights) of the nicotine and internal standard (4.4). Carry out the determination at least twice.Calculate the ratio of the nicotine peak to the internal standard peak from the peak area (or height) data for each of the calibration solutions. Plot the graph of the

44、nicotine concentrations in accordance with the area ratios, and calculate a linear regression equation (concentration of nicotine according to the area ratios) from these data. The graph should be linear and the regression line should pass through the origin. Use the slope of the regression equation

45、.Perform this full calibration procedure daily. In addition, inject an aliquot of an intermediate concentration standard after every 20 sample determinations. If the calculated concentration for this solution differs by more than 3 % from the original value, repeat the full calibration procedure.6.4

46、 DeterminationInject aliquots (2 l) of the test portion (see 6.1) into the gas chromatograph. Calculate the ratio of the nicotine peak/internal standard peak from the peak area (or height) data.Carry out two determinations on the same test portion (see 6.1).Calculate the mean value of the ratio from

47、 the two determinations.Where results are obtained from a number of separate channels of smoking and where an auto-sampler is used, a single aliquot portion from the smoke traps is considered adequate.7 Expression of resultsCalculate the concentration of nicotine in the test portion using the graph

48、or linear regression equation prepared in 6.3. From the concentration of nicotine in the test portion, calculate the amount of nicotine in the smoke condensate. Deduce the amount in the cigarettes smoked. Express the test results in milligrams per cigarette, mN, for each channel to the nearest 0,01

49、mg and the average per cigarette to the nearest 0,1 mg.8 Repeatability and reproducibilityA major international collaborative study involving 30 laboratories and 6 samples, conducted in 1990, showed that when cigarettes are smoked in accordance with ISO 4387 and the resulting smoke solutions ISO 2013 All rights reserved 3BS ISO 10315:2013ISO 10315:2013(E)are analysed by this method, the following values for the repeatability limits (r) and the reproducibility limits (R) are obtained.The difference between two s