BS EN 15199-4:2021 – TC:2022 Edition
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Tracked Changes. Petroleum products. Determination of boiling range distribution by gas chromatography method – Light fractions of crude oil
Published By | Publication Date | Number of Pages |
BSI | 2022 | 62 |
This document specifies a method for the determination of the boiling range distribution of petroleum products by capillary gas chromatography using flame ionization detection. This document is applicable to stabilized crude oils and for the boiling range distribution and the recovery up to and including n-nonane. A stabilized crude oil is defined as having a Reid Vapour Pressure equivalent to or less than 82,7 kPa as determined by IP 481 [3].
Annex C specifies an algorithm for merging the boiling point distribution results obtained using this method with the results obtained with EN 15199-3 . This will result in a boiling range distribution and recovery up to C120.
There is no specific precision statement for the combined results obtained after merging the results of EN 15199?3 and EN 15199?4 . For the precision of the boiling range distribution up to n-nonane, the precision statement of EN 15199?4 applies. For the precision of the boiling range distribution from n-nonane through C120, the precision of EN 15199?3 applies.
For the purposes of this document, the terms “% ( m/ m)” and “% ( V/ V)” are used to represent respectively the mass fraction, ?, and the volume fraction, ?.
The use of this document can involve hazardous materials, operations and equipment. This document does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this document to take appropriate measures to ensure safety and health of personnel prior to application of the document and fulfil statutory and regulatory requirements for this purpose.
PDF Catalog
PDF Pages | PDF Title |
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1 | 30447092 |
27 | A-30419040 |
28 | undefined |
32 | 1 Scope 2 Normative references 3 Terms and definitions |
33 | 4 Principle 5 Reagents and materials 6 Apparatus 6.1 Analytical balance capable of weighing to the nearest 0,1 mg 6.2 Gas chromatograph |
34 | 6.3 Detector |
35 | 6.4 Pre-column configurations 6.4.1 Heated valve switching box (see Figure B.1) 6.4.2 Injection port (see Figure B.2 and B.3) 6.5 Analytical column 6.5.1 General 6.5.2 Resolution |
36 | 6.6 Skewness 6.7 Data collection |
37 | 7 Sampling and sample handling 8 Calculation of response factors |
38 | 9 Procedure 9.1 Sample preparation 9.2 Determination of backflush time 9.2.1 Initial work 9.2.2 Analytical column 9.2.3 Accelerated analytical column |
39 | 9.3 Sample analysis 9.3.1 Initial work 9.3.2 Calculation of individual components results |
40 | 9.3.3 Boiling point distribution of fraction up to and including nonane 10 Reporting 11 Precision 11.1 General 11.2 Repeatability, r 11.3 Reproducibility, R |
41 | 12 Test report |
42 | Annex A (informative)Analysis assistance |
49 | Annex B (informative)Apparatus configuration |
51 | Annex C (normative)Algorithm for merging boiling point distribution results of EN 151993 and EN 151994 C.1 General C.2 Summary of the procedure C.3 EN 151993 and EN 151994 data accuracy determination |
52 | C.4 Elements required to perform merge of EN 151994 and EN 151993 at the merge point C.4.1 General C.4.2 EN 151994 mass percent by BP value array, N Elements |
53 | C.4.3 EN 151993 mass percent by BP data array, N elements |
54 | C.5 Data merging procedure |
55 | C.6 Reporting merged results |
58 | C.7 Normalizing results for recoveries in excess of 100 % by mass after merging |
60 | Blank Page |