BSI PD CEN/TS 18044:2024
$189.07
Ambient air. Determination of the concentration of levoglucosan. Chromatographic method
Published By | Publication Date | Number of Pages |
BSI | 2024 | 46 |
This document specifies a chromatographic method for the determination of levoglucosan in aqueous or organic extracts of filter samples collected in accordance with EN 12341:2023 [5]. The method has been tested for concentrations of ca. 10 ng/m3 up to ca. 3 000 ng/m3 with a sampling duration of 24 h. The procedure is also suitable for the determination of galactosan and mannosan. Depending on the analysis instrumentation used, the carbohydrates inositol, glycerol, threitol/erythritol, xylitol, arabitol, sorbitol, mannitol, threalose, mannose, glucose, galactose and fructose can also be determined. However, no performance characteristics are given for these compounds in this document.
PDF Catalog
PDF Pages | PDF Title |
---|---|
2 | undefined |
8 | 1 Scope 2 Normative references 3 Terms and definitions 4 Symbols and abbreviations |
9 | 5 Principle 6 Equipment 6.1 Sampling 6.1.1 Sampling device 6.1.2 Particle filter 6.2 Apparatus for sample preparation 6.3 Analytical equipment 6.3.1 IC-PAD |
10 | 6.3.2 GC-MS 6.4 Chemicals and accessories |
11 | 7 Sampling 8 Sample preparation and analysis 8.1 General 8.2 IC-PAD method 8.2.1 Sample preparation 8.2.2 Eluent preparation 8.2.3 Analysis 8.2.4 Calibration |
12 | 8.3 GC-MS method 8.3.1 Sample preparation 8.3.2 Analysis 8.3.3 Calibration 9 Calculation of results |
13 | 10 Measurement uncertainty 10.1 General 10.2 Evaluation according to ISO 57252 |
14 | 10.3 Evaluation of laboratory data according to ISO/IEC Guide 98-3 |
15 | 11 Limit of detection and limit of quantification |
16 | 12 Interferences 12.1 General 12.2 IC-PAD |
17 | 12.3 GC-MS 13 Quality assurance and quality control |
18 | Annex A (informative)Application examples of the IC-PAD method A.1 Example 1 A.1.1 Apparatus A.1.2 Operating parameters |
19 | A.1.3 Chemicals and accessories |
20 | A.1.4 Procedure A.1.4.1 Calibration standards A.1.4.2 Eluent preparation A.1.4.3 Sample preparation |
21 | A.1.4.4 Preparation of instrumentation A.1.4.5 Analysis A.1.4.6 Limits of detection |
22 | A.1.4.7 Chromatograms |
23 | A.2 Example 2 A.2.1 Apparatus |
24 | A.2.2 Operating parameters A.2.3 Chemicals and accessories |
25 | A.2.4 Procedure A.2.4.1 Calibration standards A.2.4.2 Eluent preparation A.2.4.3 Sample preparation |
26 | A.2.4.4 Preparation of instrumentation A.2.4.5 Separation and detection conditions |
27 | A.2.4.6 Analysis A.2.4.7 Analysis validation A.2.4.8 Limits of detection |
28 | A.2.4.9 Chromatograms |
30 | Annex B (informative)Application example of the GC-MS method B.1 Apparatus B.2 GC/MS operating parameters B.3 Chemicals |
31 | B.4 Procedure B.4.1 Calibration standards |
32 | B.4.2 Sample preparation B.4.2.1 Spiking the samples with surrogate standard B.4.2.2 Ultrasonic extraction B.4.2.3 Derivatisation B.4.2.4 Analysis |
34 | Annex C (informative)Calculation of the measurement uncertainty using results of a laboratory intercomparison C.1 General C.2 Calculations according to ISO 57252 |
35 | C.3 Calculation of uncertainty parameters according to ISO 13528 (Q/Hampel method) |
36 | C.4 Comparison of the two calculation methods |
39 | Annex D (informative)Possible requirements for the uncertainty of single steps in work up and analysis for an overall uncertainty of 40 % |
41 | Annex E (informative)Calculation of the limit of detection from the calibration function |
42 | Annex F (informative)Illustrative chromatograms |