BS EN 15199-4:2015
$142.49
Petroleum products. Determination of boiling range distribution by gas chromatography method – Light fractions of crude oil
Published By | Publication Date | Number of Pages |
BSI | 2015 | 26 |
This European Standard describes a method for the determination of the boiling range distribution of petroleum products by capillary gas chromatography using flame ionization detection. This European Standard 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].
For the purposes of this European Standard, the terms “% (m/m)” and “% (V/V)” are used to represent respectively the mass fraction, ω, and the volume fraction, φ.
The use of this European Standard can involve hazardous materials, operations and equipment. This European Standard does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this standard to take appropriate measures to ensure safety and health of personnel prior to application of the standard, and fulfil statutory and regulatory requirements for this purpose.
PDF Catalog
PDF Pages | PDF Title |
---|---|
5 | European foreword |
6 | 1 Scope 2 Normative references 3 Terms and definitions 4 Principle 5 Reagents and materials |
7 | 6 Apparatus 6.1 Analytical balance 6.2 Gas chromatograph 6.3 Detector 6.4 Pre-column configurations 6.4.1 Heated valve switching box (see Figure B.1) |
8 | 6.4.2 Injection port (see Figure B.2 and B.3) Table 1 —Typical chromatographic conditions 6.5 Analytical column 6.5.1 General |
9 | 6.5.2 Resolution Figure 1 —Determination of resolution 6.6 Skewness |
10 | Figure 2 —Calculation of peak skewness 6.7 Data collection 7 Sampling and sample handling 8 Calculation of response factors |
11 | Table 2 — Calculated response factors for hydrocarbons 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 |
12 | Figure 3 — Example chromatogram showing elution for determining backflush time 9.3 Sample analysis 9.3.1 Initial work 9.3.2 Calculation of individual components results |
13 | 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 |
14 | 12 Test report |
15 | Annex A (informative) Analysis assistance Table A.1 — Example report of an analysis |
20 | Figure A.1 — Example chromatograms belonging to report data of Table A.1 |
21 | Annex B (informative) Apparatus configuration Figure B.1 — Typical configuration using a heated valve switching box |
22 | Figure B.2 — Typical configuration with direct connection to the capillary column Figure B.3 — Typical configuration with a connection via a splitter to the capillary column |
23 | Bibliography |