DIN EN ISO 1833-16-2011 Textiles - Quantitative chemical analysis - Part 16 Mixtures of polypropylene fibres and certain other fibres (method using xylene) (ISO 1833-16 2006) Germa.pdf

1、January 2011 Translation by DIN-Sprachendienst.English price group 7No part of this translation may be reproduced without prior permission ofDIN Deutsches Institut fr Normung e. V., Berlin. Beuth Verlag GmbH, 10772 Berlin, Germany,has the exclusive right of sale for German Standards (DIN-Normen).ICS

2、 59.060.20!$l“1739897www.din.deDDIN EN ISO 1833-16Textiles Quantitative chemical analysis Part 16: Mixtures of polypropylene fibres and certain other fibres(method using xylene) (ISO 1833-16:2006)English translation of DIN EN ISO 1833-16:2011-01Textilien Quantitative chemische Analysen Teil 16: Misc

3、hungen aus Polypropylenfasern und bestimmten anderen Fasern(Xylol-Verfahren) (ISO 1833-16:2006)Englische bersetzung von DIN EN ISO 1833-16:2011-01Textiles Analyse chimique quantitative Partie 16: Mlanges de fibres de polypropylne et de certaines autres fibres (mthode auxylne) (ISO 1833-16:2006)Tradu

4、ction anglaise de DIN EN ISO 1833-16:2011-01SupersedesDIN 54215:1977-12www.beuth.deDocument comprises pagesIn case of doubt, the German-language original shall be considered authoritative.1002.11 DIN EN ISO 1833-16:2011-01 A comma is used as the decimal marker. National foreword This standard has be

5、en prepared by Technical Committee ISO/TC 38 “Textiles” in collaboration with Technical Committee CEN/TC 248 “Textile and textile products” (Secretariat: BSI, United Kingdom). The responsible German body involved in its preparation was the Normenausschuss Materialprfung (Materials Testing Standards

6、Committee), Working Committee NA 062-05-12 AA Textilchemische Prfver-fahren und Fasertrennung. The Introduction of ISO 1833-1 is summarized below as a help to users of this standard: In general, the methods described in the various parts of ISO 1833 are based on the selective solution of an individu

7、al component. Once a component is dissolved from a test specimen, the insoluble residue is weighed and the percentage of the soluble component(s) is calculated from loss in mass. ISO 1833-1 gives information that is common to all of these analytical methods for all fibre mixtures, regardless of thei

8、r composition. This general information should be used when applying the other parts of the ISO 1833 series; each of these parts contains a more detailed description of a method that is applicable for a specific fibre mixture. If one of these methods is based on a principle other than selective solu

9、tion, this is expressly stated and described in detail in the respective part of the standards series. Fibre mixtures used during processing and, to a lesser extent, in finished textiles may contain fats, waxes or dressings which either occur naturally or are added to facilitate processing. Fibre mi

10、xtures may also contain salts and other water-soluble matter. Some or all of these substances can separate during analysis and be erroneously calculated as soluble fibre components. To avoid this error, non-fibrous matter should be removed before analysis. A method of pre-treatment for removing oils

11、, fats, waxes and water-soluble matter is given in ISO 1833-1:2006, Annex A. In addition, textiles may contain resins or other matter added to bind the fibres or to confer special properties, such as water repellence or crease resistance. Such matter, including dyestuffs in exceptional cases, may in

12、terfere with the action of the reagent on the soluble components and/or may be partially or completely removed by the reagents. This type of added matter can thus also cause errors and should be removed before the sample is analysed. If it is impossible to remove such added matter, the methods are n

13、o longer applicable. Dye in dyed fibre is considered to be an integral part of the fibre and is not removed. Most textile fibres contain water, the amount of which depends on the type of fibre and the relative humidity of the ambient air. These analyses are conducted on the basis of dry mass, and a

14、procedure for determining the dry mass of analytical samples and residues is given in ISO 1833-1. The result is thus obtained on the basis of the dry mass of the dry fibres only. 2 DIN EN ISO 1833-16:2011-01 Provisions have been made for recalculating results on the basis of a) permissible deviation

15、s agreed upon for moisture content1)b) permissible deviations agreed upon for humidity, as well as for 1) the fibrous matter separated during pre-treatment, and 2) non-fibrous matter (e.g. dressings, processing oils or sizing assistants) which can be considered as being a commonly used commercial ar

16、ticle that is part of the fibre. In some methods, the insoluble components of a mixture may be partially dissolved in the reagent used to dissolve the soluble component(s). Whenever possible, reagents have been chosen that have little or no effect on the insoluble fibres. If a loss in mass is known

17、to occur during the analysis, the result should be corrected; correction factors are given for this purpose. These factors have been determined in several laboratories by treating, with the appropriate reagent as specified in the method of analysis, fibres cleaned by pre-treatment. These correction

18、factors apply only to undegraded fibres. If the fibres have been degraded during processing, different correction factors may be necessary. The methods described in this series apply for single determinations; at least two determinations should be made on separate samples, further determinations can

19、 be made where desired. Before the analyses are carried out, all fibres in the mixture should be identified. For the purposes of confirmation, it is recommended that alternative methods be used in which the component that would have made up the residue when using the standard method is dissolved fir

20、st, unless this is not technically possible. Where practically possible, the components of a mixture are to be manually separated if the method described in ISO 1833-1:2006, Annex B is to be primarily used instead of the chemical analytical methods described in the other parts of ISO 1833. The DIN S

21、tandard corresponding to the International Standard referred to in this document is as follows: ISO 1833-1 DIN EN ISO 1833-1 Amendments This standard differs from DIN 54215:1977-12 as follows: a) the text of ISO 1833-16 has been adopted. Previous editions DIN 54215: 1977-12 1) Commonly used conditio

22、ning values shall be used for each fibre, where these are available. 3 DIN EN ISO 1833-16:2011-01 National Annex NA (informative) Bibliography DIN EN ISO 1833-1, Textiles Quantitative chemical analysis Part 1: General principles of testing 4 EUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 1

23、833-16 October 2010 ICS 59.060.01 English Version Textiles - Quantitative chemical analysis - Part 16: Mixtures of polypropylene fibres and certain other fibres (methodusingxylene) (ISO 1833-16:2006) Textiles - Analyse chimique quantitative - Partie 16: Mlanges de fibres de polypropylne et de certai

24、nes autres fibres (mthode au xylne) (ISO 1833-16:2006) Textilien - Quantitative chemische Analysen - Teil 16: Mischungen aus Polypropylenfasern und bestimmten anderen Fasern (Xylol-Verfahren) (ISO 1833-16:2006) This European Standard was approved by CEN on 12 September 2010. CEN members are bound to

25、 comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN Ma

26、nagement Centre or to any CEN member. This European Standard exists in three official versions (English, French, German). A version in any other language made by translation under the responsibility of a CEN member into its own language and notified to the CEN Management Centre has the same status a

27、s the official versions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Ro

28、mania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG Management Centre: Avenue Marnix 17, B-1000 Brussels 2010 CEN All rights of exploitation in any form and by any means reserve

29、d worldwide for CEN national Members. Ref. No. EN ISO 1833-16:2010: EDIN EN ISO 1833-16:2011-01 EN ISO 1833-16:2010 (E) 2Contents Page Foreword .3 1 Scope.5 2 Normative references.5 3 Principle 5 4 Reagents .5 5 Apparatus5 6 Test Procedure .6 7 Calculation and expression of results .6 8 Precision .6

30、 EN ISO 1833 consists of the following parts, under the general title Textiles Quantitative chemical analysis: Part 1: General principles of testing Part 2: Ternary fibre mixtures Part 3: Mixtures of acetate and certain other fibres (method using acetone) Part 4: Mixtures of certain protein and cert

31、ain other fibres (method using hypochlorite) Part 5: Mixtures of viscose, cupro or modal and cotton fibres (method using sodium zincate) Part 7: Mixtures of polyamide and certain other fibres (method using formic acid) Part 8: Mixtures of acetate and triacetate fibres (method using acetone) Part 9:

32、Mixtures of acetate and triacetate fibres (method using benzyl alcohol) Part 10: Mixtures of triacetate or polylactide and certain other fibres (method using dichloromethane) Part 11: Mixtures of cellulose and polyester fibres (method using sulfuric acid) Part 12: Mixtures of acrylic, certain modacr

33、ylics, certain chlorofibres, certain elastanes and certain other fibres (method using dimethylformamide) Part 13: Mixtures of certain chlorofibres and certain other fibres (method using carbon disulfide/acetone) Foreword The text of ISO 1833-16:2006 has been prepared by Technical Committee ISO/TC 38

34、 “Textiles” of the International Organization for Standardization (ISO) and has been taken over as EN ISO 1833-16:2010 by Technical Committee CEN/TC 248 “Textiles and textile products” the secretariat of which is held by BSI. This European Standard shall be given the status of a national standard, e

35、ither by publication of an identical text or by endorsement, at the latest by April 2011, and conflicting national standards shall be withdrawn at the latest by April 2011. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/o

36、r CENELEC shall not be held responsible for identifying any or all such patent rights. Part 6: Mixtures of viscose or certain types of cupro or modal or lyocell and cotton fibres (method using formic acid and zinc chloride) Part 14: Mixtures of acetate and certain chlorofibres (method using acetic a

37、cid) Part 15: Mixtures of jute and certain animal fibres (method by determining nitrogen content) Part 16: Mixtures of polypropylene fibres and certain other fibres (method using xylene) Part 17: Mixtures of chlorofibres (homopolymers of vinyl chloride) and certain other fibres (method using sulfuri

38、c acid) Part 18: Mixtures of silk and wool or hair (method using sulfuric acid) DIN EN ISO 1833-16:2011-01 EN ISO 1833-16:2010 (E) 3 Part 19: Mixtures of cellulose fibres and asbestos (method by heating) Part 21: Mixtures of chlorofibres, certain modacrylics, certain elastanes, acetates, triacetates

39、 and certain other fibres (method using cyclohexanone) The following parts are under preparation: Part 22: Mixtures of viscose or certain types of cupro or modal or lyocell and flax fibres (method using formic acid and zinc chlorate) Part 23: Mixtures of polyethylene and polypropylene (method using

40、cyclohexanone) Part 24: Mixtures of polyester and some other fibres (method using phenol and tetrachloroethane) According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria

41、, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingdom. Endorsement notice The

42、 text of ISO 1833-16:2006 has been approved by CEN as a EN ISO 1833-16:2010 without any modification. Part 20: Mixtures of elastane and certain other fibres (method using dimethylacetamide) DIN EN ISO 1833-16:2011-01 EN ISO 1833-16:2010 (E) 41 Scope This part of ISO 1833 specifies a method, using xy

43、lene, to determine the percentage of polypropylene, after removal of non-fibrous matter, in textiles made of binary mixtures of polypropylene fibres and wool, animal hair, silk, cotton, viscose, cupro, modal, acetate, triacetate, polyamide, polyester, acrylic and glass fibres. 2 Normative references

44、 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) applies. ISO 1833-1, Textiles Quantitative chemical analy

45、sis Part 1: General principles of testing 3 Principle The polypropylene fibre is dissolved from a known dry mass of the mixture with boiling xylene. The residue is collected, washed, dried and weighed; its mass, corrected if necessary, is expressed as a percentage of the dry mass of the mixture. The

46、 percentage of polypropylene is found by the difference. 4 Reagents Use the reagent described in ISO 1833-1 as light petroleum together with that given in 4.1. 4.1 Xylene, distilling between 137 C and 142 C. SAFETY PRECAUTIONS The harmful effects of this reagent shall be borne in mind, and full prec

47、autions shall be taken during use. 5 Apparatus Use the apparatus described in ISO 1833-1 together with those given in 5.1 and 5.2. 5.1 Conical flasks, of minimum capacity 200 ml, glass stoppered. 5.2 Reflux condenser, suitable for liquids of high boiling point, fitting the conical flasks. DIN EN ISO

48、 1833-16:2011-01 EN ISO 1833-16:2010 (E) 56 Test procedure Follow the general procedure given in ISO 1833-1, and then proceed as follows. Preheat the filter crucible through which the xylene is to be filtered. To the specimen contained in the conical flask, add 100 ml of the xylene per gram of specimen. Attach the condenser and boil the contents for 3 min. Decant the hot liquid through the weighed filter crucible. Repeat this treatment twice more, each time using a fresh 50 ml po