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1. The value of microscopy analysis Garry BurdettHealth and Safety LaboratoryHarpur Hill, Buxton, UK, SK17 9JN
2. Asbestos Hazard Mortality (excess deaths) due to:
Fibrosis of the lung (asbestosis)
Cancer of the lung (bronchial cancer etc)
Cancer of the lung lining (e.g. mesothelioma)
Morbidity (lung changes/dysfunction)
Pleural plaques;
Diffuse pleural effusions
3. Fibre Related Risk: Depends on:
Dimensions
Durability / Type
Dose / Exposure
Time
(Measurable by microscopy)
4. EU Directive: Dimensions For the purposes of measuring in the air, only fibres with a length of more than five micrometres, a breadth of less than three micrometres and a length to breadth ratio greater than 3:1 shall be taken into consideration.
(2003/18/EC amending to EU asbestos worker protection directive (83/477/EEC) article 7.6 )
5. Durability / Type
6. Dose / Exposure Exposure is used as a surrogate for dose by sampling a known volume of air onto a membrane filter and counting the numbers of fibres present in a known area.
This is used to calculate the fibre concentration in f/ml or f/cm3 of air.
Uses size criteria to determine ability to reach pulmonary region of the lung.
7. Time Dose = exposure x duration (f/ml/years)
Risk µ cumulative dose (assume linear);
Risk µ time since first exposure (mesothelioma related by power law).
Lag time 15 – 60 years from exposure to disease symptoms
8. EU directive: Fibre Counting “Fibre counting shall be carried out whenever possible by PCM (Phase contrast microscope) in accordance with the 1997 (World Health Organisation) recommended method (16) or any other method giving equivalent results.”
9. EU Directive: Requirements The 2003 amendment to 83/477/EEC abandoned action levels and different control levels for different types of asbestos and introduced a single limit of 0.1 f/ml over an 8-hour time weighted average. (Article 8)
Therefore the EU regulation for controlling the risk to workers, require only PCM fibre number information over a broadly defined size range.
Article 4 requires the type and quantities of asbestos handled to be notified
10. Main types of microscopy for fibre counting. Phase contrast light microscopy PCM
Scanning electron microscopy SEM
Transmission electron microscopy TEM.
All have ISO or WHO standard methods
Polarised light microscopy PLM for bulk analysis.
12. PCM (X500 magnification)
13. SEM
14. TEM
15. SEM higher Mag & 3D
16. TEM high mag chrystotile
17. PLM : Dispersion staining
18. Discrimination of fibre type PCM: No discrimination or identification ;
PLM Uses optical properties + refractive index/ dispersion colours to identify fibres; >0.8µm width;
SEM uses Energy Dispersive X-ray analysis to semi-quantitatively measure chemistry;
TEM uses quantitative EDX and electron diffraction to identify fibres.
20. Comparison of methods for fibre counting
21. Likely upper limit of detection (f/ml) by method and volume
22. Accuracy & Precision Accuracy not usually known.
Precision includes:
Random “Poisson” counting error
Instrumental errors (QA / calibration)
Human errors (QA / Proficiency testing)
23. Random counting errors (95%)
24. Quality and accreditation Quality assurance and proficiency testing is essential, particularly if results from different analysts and laboratories are being used or compared.
Accreditation of Laboratories to ISO 17025 mandated by the EU directive.
26. RICE: Fibre counting PT RICE - 187 labs.
MMMF – 12 labs.
ERM – WHO major change
27. AIMS: Fibre Identification PT
28. Value of PCM counting Workplace exposure can be controlled using the WHO - PCM method;
Counts “regulated” WHO fibres & meets EU criteria;
Relatively quick (on-site) and cheap;
Environmental exposure can be screened by PCM.
29. PCM Limitations PCM has limited detection due to background counts on blank filters (0.01 f/ml);
No knowledge of fibre types;
Only an “index of exposure”
30. Value of analytical SEM Can be adjusted to give regulated fibre counts,
Can give fibre size information,
Classifies fibre types present using EDX spectra data.
31. SEM limitations Limited availability;
Off site analysis;
Costly
Can only be used for regulated fibre counting,
No definitive identification of fibres,
Lowest area of filter scanned per field of view.
32. Value of TEM Can count regulated fibres + all fibre sizes.
Accurate size information,
EDX chemical analysis of all fibre sizes
Crystal structure information (SAED)
Identification of fibre type,
Can give complete information on all fibre sizes if needed
33. Limitations of TEM Limited availability;
Off site;
Costly
34. Recommendations 1 Use PCM for workplace control and checking after clean –up (with disturbance sampling).
Indoor and near source environmental use PCM screening and SEM or TEM analysis (as necessary) on selected half-filters.
Ambient air: Analytical TEM is best, SEM is more limited, PCM not very useful.
35. Recommendations 2 Use Polarised light microscopy (PLM) for analysis of bulk samples for asbestos present and type of asbestos.
Use PLM to screen minerals and soils for asbestos content.
Asbestos in water usually analysed by TEM