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BS EN ISO 22854:2016

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Liquid petroleum products. Determination of hydrocarbon types and oxygenates in automotive-motor gasoline and in ethanol (E85) automotive fuel. Multidimensional gas chromatography method
Available format(s)

Hardcopy , PDF

Superseded date

08-06-2021

Language(s)

English

Published date

04-30-2016

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Principle
5 Reagents and materials
6 Apparatus
7 Sampling
8 Procedure
9 Calculation
10 Expression of results
11 Precision
12 Test report
Annex A (informative) - Instrument specifications
Annex B (informative) - Examples of typical chromatograms
Bibliography

Defines the gas chromatographic (GC) method for the determination of saturated, olefinic and aromatic hydrocarbons in automotive motor gasoline and ethanol (E85) automotive fuel.

This International Standard specifies the gas chromatographic (GC) method for the determination of saturated, olefinic and aromatic hydrocarbons in automotive motor gasoline and ethanol (E85) automotive fuel. Additionally, the benzene content, oxygenate compounds and the total oxygen content can be determined. NOTE1 For the purposes of this document, the terms% ( m/m) and% ( V/V) are used to represent respectively the mass fraction, µ, and the volume fraction, φ. This International Standard defines two procedures, A and B. Procedure A is applicable to automotive motor gasoline with total aromatics of up to 50% ( V/V); total olefins from about 1,5% ( V/V) up to 30% ( V/V); oxygenates from 0,8% ( V/V) up to 15% ( V/V); total oxygen from about 1,5% ( m/m) to about 3,7% ( m/m); and benzene of up to 2% ( V/V). The system can be used for ethers with 5 or more C atoms up to 22% ( V/V) but the precision has not been established up to this level. Although this test method can be used to determine higher-olefin contents of up to 50% ( V/V), the precision for olefins was tested only in the range from about 1,5% ( V/V) to about 30% ( V/V). Although specifically developed for the analysis of automotive motor gasoline that contains oxygenates, this test method can also be applied to other hydrocarbon streams having similar boiling ranges, such as naphthas and reformates. NOTE2 For Procedure A, precision data have been established for the oxygenate compounds in automotive motor gasoline samples containing ethyl-tert-butyl ether (ETBE), methyl-tert-butyl ether (MTBE), tert-amylmethyl ether (TAME), iso-propanol, iso-butanol, tert-butanol, methanol and ethanol. The derived precision data for methanol do not comply with the precision calculation as presented in this International Standard. Applicability of this International Standard has also been verified for the determination of n-propanol, acetone, and di-isopropyl ether (DIPE). However, no precision data have been determined for these compounds. Procedure B describes the procedure for the analysis of oxygenated groups (ethanol, methanol, ethers, C3– C5 alcohols) in ethanol (E85) automotive fuel containing ethanol between 50% ( V/V) and 85% ( V/V). The gasoline is diluted with an oxygenate-free component to lower the ethanol content to a value below 20% ( V/V) before the analysis by GC. If the ethanol content is unknown, it is advisable to use a dilution of 4:1 when analysing the sample. The sample can be fully analysed including hydrocarbons. Precision data for the diluted sample are only available for the oxygenated groups. NOTE3 For Procedure B, the precision can be used for an ethanol fraction from about 50% ( V/V) up to 85% ( V/V). For the ether fraction, the precision as specified in Table6 can be used for samples containing at least 11% ( V/V) of ethers. For the higher alcohol fraction, too few data were obtained to derive a full precision statement and the data presented in Table6 are therefore only indicative. NOTE4 While developing this test method, the final boiling point was limited to 215°C. NOTE5 An overlap between C9 and C10 aromatics can occur. However, the total is accurate. Isopropyl benzene is resolved from the C8 aromatics and is included with the other C9 aromatics.

Committee
PTI/13
DevelopmentNote
Supersedes BS EN 14517 & 06/30149412 DC. (02/2009) Supersedes BS 2000-526(2004). (03/2009) Supersedes 12/30263877 DC. (07/2014) Also numbered as BS 2000-566(2016). Supersedes BS 2000-566(2014). (05/2016)
DocumentType
Standard
Pages
30
PublisherName
British Standards Institution
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
ISO 22854:2016 Identical
EN ISO 22854:2016 Identical

ISO 3171:1988 Petroleum liquids — Automatic pipeline sampling
CEN/TR 15745:2015 LIQUID PETROLEUM PRODUCTS - DETERMINATION OF HYDROCARBON TYPES AND OXYGENATES VIA MULTIDIMENSIONAL GAS CHROMATOGRAPHY METHOD - ROUND ROBIN RESEARCH REPORT
EN 1601:2017 Liquid petroleum products - Determination of organic oxygenate compounds and total organically bound oxygen content in unleaded petrol - Method by gas chromatography (O-FID)
EN 228:2012+A1:2017 Automotive fuels - Unleaded petrol - Requirements and test methods
ISO 3170:2004 Petroleum liquids — Manual sampling
ASTM D 6839 : 2017-06 TEST METHOD FOR HYDROCARBON TYPES, OXYGENATED COMPOUNDS, AND BENZENE IN SPARK IGNITION ENGINE FUELS BY GAS CHROMATOGRAPHY
ISO 4259:2006 Petroleum products Determination and application of precision data in relation to methods of test
EN 13132:2000 Liquid petroleum products - Unleaded petrol - Determination of organic oxygenate compounds and total organically bound oxygen content by gas chromatography using column switching

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