EN 16423-2012 en Liquefied petroleum gases - Determination of dissolved residue - Gas chromatographic method using liquid on-column injection《液化石油气 溶渣测定 用液体的气相色谱柱头注射法》.pdf

《EN 16423-2012 en Liquefied petroleum gases - Determination of dissolved residue - Gas chromatographic method using liquid on-column injection《液化石油气 溶渣测定 用液体的气相色谱柱头注射法》.pdf》由会员分享，可在线阅读，更多相关《EN 16423-2012 en Liquefied petroleum gases - Determination of dissolved residue - Gas chromatographic method using liquid on-column injection《液化石油气 溶渣测定 用液体的气相色谱柱头注射法》.pdf（28页珍藏版）》请在麦多课文档分享上搜索。

1、BSI Standards PublicationBS EN 16423:2013Liquefied petroleumgases Determination ofdissolved residue Gaschromatographic method usingliquid, on-column injectionBS EN 16423:2013 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN 16423:2013. The UK participation in its

2、 preparation was entrusted to TechnicalCommittee PTI/13, Petroleum Testing and Terminology.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include all the necessary provisions of a contract. Users are responsible

3、for its correct application. The British Standards Institution 2013.Published by BSI Standards Limited 2013ISBN 978 0 580 78988 5ICS 75.160.20Compliance with a British Standard cannot confer immunity from legal obligations.This British Standard was published under the authority of the Standards Poli

4、cy and Strategy Committee on 31 October 2013.Amendments/corrigenda issued since publicationDate T e x t a f f e c t e dBS EN 16423:2013EUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN 16423 October 2013 ICS 75.160.20 English Version Liquefied petroleum gases - Determination of dissolved residue

5、-Gas chromatographic method using liquid, on-column injectionGaz de ptrole liqufi - Dtermination des rsidus dissous - Mthode par chromatographie en phase gazeuse avec injection liquide on-column Flssiggas - Bestimmung gelster Rckstnde - Gaschromatographisches Prfverfahren durch Direkteinspritzung vo

6、n Flssigkeit auf die Sule This European Standard was approved by CEN on 31 August 2013. CEN members are bound to 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 list

7、s and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC Management 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

8、the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yug

9、oslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPE

10、N DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2013 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 16423:2013: EBS EN 16423:2013EN 16423:2013 (E) 2 Contents Page

11、Foreword 3 Introduction .4 1 Scope 5 2 Normative references 5 3 Terms and definitions .5 4 Principle 5 5 Reagents and materials 5 6 Apparatus .6 7 Sampling 10 8 Preparation of apparatus . 10 9 Test procedure 11 9.1 Safety and hazards . 11 9.2 Summary of the method . 11 9.3 Calibration . 11 9.4 Proce

12、dure 12 10 Calculations . 13 11 Quality control . 14 12 Expression of results . 14 13 Precision 14 13.1 General . 14 13.2 Repeatability 14 13.3 Reproducibility 15 14 Test report . 15 Annex A (normative) Density calculation of the LPG and correction of the result . 16 Annex B (informative) Quality co

13、ntrol monitoring 19 Annex C (informative) Analysis of benzene, toluene and hydrocarbons C7through C10. 20 Annex D (informative) Analysis of di-iso-propanolamine 22 Annex E (informative) FID linearity check 23 Bibliography . 24 BS EN 16423:2013EN 16423:2013 (E) 3 Foreword This document (EN 16423:2013

14、) has been prepared by Technical Committee CEN/TC 19 “Gaseous and liquid fuels, lubricants and related products of petroleum, synthetic and biological origin”, the secretariat of which is held by NEN. This European Standard shall be given the status of a national standard, either by publication of a

15、n identical text or by endorsement, at the latest by April 2014 and conflicting national standards shall be withdrawn at the latest by April 2014. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be hel

16、d responsible for identifying any or all such patent rights. According to the CEN/CENELEC Internal Regulations, the national standards organisations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia

17、, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. BS EN 16423:2013EN 16423:2

18、013 (E) 4 Introduction Control over the residue content as specified in EN 589 is of considerable importance in end-use applications of Liquefied Petroleum Gas (LPG). Dissolved residual matter, also known as evaporation residue, in LPG is contamination which can occur during production, transportati

19、on or storage. This standard has been developed as a potential replacement of the commonly used methods, as this method of determination: is quicker and much more sensitive than manual methods, such as ASTM D2158 1 or EN 15471 2, which are based on evaporation of (large) sample volumes followed by v

20、isual or gravimetric estimation of residue content; provides enhanced sensitivity in measurements of heavier (evaporation) residues compared to EN 15470 3, with a quantification limit of 10 mg/kg total residue; gives both quantitative results and information about contaminant composition such as boi

21、ling point range and fingerprint, which can be very useful in tracing the source of a particular contaminant. BS EN 16423:2013EN 16423:2013 (E) 5 1 Scope This European Standard specifies a method for the determination of the dissolved residual matter, also known as evaporation residue, in liquefied

22、petroleum gases (LPG), by gas chromatography in the range of (10 to 600) mg/kg (ppm mass). This test method quantifies soluble organic compounds (hydrocarbon materials), sometimes called evaporation residue, which can be present in liquefied petroleum gases and which are substantially less volatile

23、than the LPG product, i.e. with a boiling point between 174 C and 522 C (C10to C40). Higher boiling materials, or materials that adhere permanently to the chromatographic column, will not be detected. WARNING This standard does not purport to address all of the safety concerns, if any, associated wi

24、th its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. 2 Normative references The following documents, in whole or in part, are normatively referenced in this docum

25、ent 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. EN 589, Automotive fuels LPG Requirements and test methods EN ISO 4257, Liquefied petroleum g

26、ases Method of sampling (ISO 4257) EN ISO 8973:1999, Liquefied petroleum gases Calculation method for density and vapour pressure (ISO 8973:1997) ISO 1998-1, Petroleum industry Terminology Part 1: Raw materials and products 3 Terms and definitions For the purposes of this document, the terms and def

27、initions given in EN 589, ISO 1998-1, and the following apply. 3.1 high pressure liquefied gas injector sample introduction device which injects liquefied gas samples under pressure and at room temperature directly onto the chromatographic column thereby maintaining the sample in liquid phase during

28、 the injection process 3.2 pressure station device that supplies high pressure inert gas to a suitable sample cylinder and therefore maintains sample in the liquid phase during the injection procedure 4 Principle A small quantity of LPG is directly transferred in liquid phase from the sample cylinde

29、r on to a GC column using a high pressure liquefied gas injector. The mixture is then analysed by capillary gas chromatography and the dissolved residue content is quantified by the external standard method. 5 Reagents and materials IMPORTANT Standards that are prepared in pentane, normally liquid a

30、t room temperature, shall be stored under refrigeration and transferred to sample cylinders prior to use. Alternatively, they can be stored in air tight cylinders. BS EN 16423:2013EN 16423:2013 (E) 6 5.1 Mineral oil in LPG calibration mixture. One of the following mixtures shall be selected for cali

31、bration: 5.1.1 Mineral oil in LPG calibration mixture, certified calibration mixture with about 50 mg/kg mineral oil in LPG. 5.1.2 Mineral oil in pentane calibration mixture. Prepare a calibration standard of mineral oil in pentane. Record the exact weighed value to the nearest mg of mineral oil and

32、 calculate the concentration in mg/kg. The concentration of the mineral oil shall be close to the expected concentration of the contamination in the LPG sample. 5.1.3 Mineral oil or local hydrocarbon fraction, boiling point range approximately C10to C40. Alternatively, a well characterised local hyd

33、rocarbon fraction, within the range C10to C40, can be used to provide quantitative and qualitative comparison to the contaminant in the sample. Care should be taken to ensure no significant fraction falls outside the C10to C40range. 5.2 Validation standard, mineral oil in pentane. Prepare a validati

34、on standard of mineral oil in pentane. Record the exact weighed value to the nearest mg of mineral oil and calculate the concentration in mg/kg. The concentration of the mineral oil shall be close to the expected concentration of the contamination in the LPG sample. 5.3 n-Alkane retention time stand

35、ard, mixture containing at least C10and C40in a concentration of (nominally) 5 mg/l each, dissolved in pentane or heptane. 5.4 Solvent, GC grade pentane. 6 Apparatus NOTE Successfully used columns and conditions are given in Table 1. 6.1 Gas chromatograph, equipped with a Large Volume Cold on Column

36、 Injector (LVOCI), linear temperature programmable column oven, and a flame ionisation detector (FID), with data acquisition and processing system. For checking the linearity of the FID one may use Annex E. 6.2 Solvent vent, controlled to allow venting the major part of the matrix. 6.3 Retention gap

37、, uncoated stainless steel capillary. 6.4 Retaining pre-column, a column with a polydimethylsiloxane stationary phase. 6.5 Analytical column, a column with a polydimethylsiloxane stationary phase. 6.6 Column coupler, coupling device suitable for leak free coupling of the retention gap to the retaini

38、ng pre-column. See Figure 1 for a schematic overview of the couplings inside the GC oven and the couplings to the solvent vent valve. BS EN 16423:2013EN 16423:2013 (E) 7 Table 1 Typical column configuration Equipment part Typical operation conditions Oven program 35 C for 3 min, 35 C to 340 C at 25

39、C/min, 340 C for 10 min Inlet program Type: cool on-column Temp: 55 C for 3 min, 55 C to 340 C at 25 C/min, 340 C for 9 min Detector settings Air flow: 400 ml/min Hydrogen flow: 40 ml/min Make up gas flow: 20 ml/min Temperature: 350 C Data rate: 20 Hz Column Retention gap: Sulfinert1 )stainless stee

40、l capillary with inner diameter 0,53 mm and length of 5 m Retaining pre-column: 3 m HP-1, 0,53 mm, 2,65 m Analytical column: HP-1, 30 m, 0,32 mm, 0,25 m Pressure station Sample flow: 2 ml/min Nitrogen pressure: 2 500 kPa Nitrogen purge pressure: 500 kPa Liquefied gas injector Injection: 25 ms 1) Sul

41、finert is a stainless steel treatment system from Restek Co., 110 Benner Circle, Bellefonte, PA 16823, USA. This information is given for the convenience of users of this European Standard and does not constitute an endorsement by CEN of the product named. Equivalent products may be used if they can

42、 be shown to lead to the same results. BS EN 16423:2013EN 16423:2013 (E) 8 6.7 Column splitter, suitable for leak-free coupling of the retaining pre-column to one side of the analytical column and the deactivated capillary on the other side. See Figure 1 for a schematic overview of the couplings ins

43、ide the GC oven and the couplings to the solvent vent valve. Key A solvent vent valve B cool on-column inlet C detector D column splitter E retention gap F retaining pre-column G analytical column Figure 1 Column overview BS EN 16423:2013EN 16423:2013 (E) 9 6.8 High pressure liquefied gas injector,

44、a high pressure valve as in Figure 2, directly connected to a needle which is inserted in the injection port of the GC, after which the valve is triggered in order to introduce a representative aliquot into the GC system without sample discrimination. Key A electrical attachment B solenoid on C valv

45、e spring D spray tip E pressurised fuel injection F injector casing G plunger Figure 2 High pressure valve BS EN 16423:2013EN 16423:2013 (E) 10 6.9 Pressure station, ensuring a sample in liquid phase at a constant pressure, with a typical configuration as in Figure 3. Key A sample cylinder B sample

46、line in C injection device D cool on column inlet E gas chromatograph F sample line out G rotometer H vaporiser I waste systemFigure 3 Typical configuration of the pressure station 7 Sampling Unless otherwise specified in the commodity specification, samples shall be taken as described in EN ISO 425

47、7 and/or in accordance with the requirements of national regulations for the sampling of the product under test. 8 Preparation of apparatus CAUTION Take all the necessary safety measures and, in particular, earth the equipment in order to eliminate the risks associated with static electricity. 8.1 G

48、as chromatograph: install and verify performance in accordance with the manufacturers instructions. Typical operating conditions are shown in Table 1. 8.2 Pressure station: install in accordance with the manufacturers instructions. Purge sample and check carefully for leaks. Connect the outlet to a

49、waste system. 8.3 High pressure liquefied gas injector: install in accordance with the manufacturers instructions. 8.4 Column configuration: install the columns as shown in Figure 1, using low dead volume connections, and check for leaks. BS EN 16423:2013EN 16423:2013 (E) 11 9 Test procedure 9.1 Safety and hazards 9.1.1 There is a significant fire hazard from LPG, and since the boiling point of LPG can be as low as -41 C, there is a risk of freezing “burns”. Take appropriate safety precautions to prevent i