
ISO 17852:2006
ISO 17852:2006 Water quality – Determination of mercury – Method using atomic fluorescence spectrometry
CDN $186.00
Description
ISO 17852:2006 specifies a method for the determination of mercury in drinking, surface, ground and rain water using atomic fluorescence spectrometry. It may be applied to industrial and municipal waste water after an additional digestion step under appropriate conditions. The potential linear dynamic range is approximately 1 nanogram per litre to 100 micrograms per litre. In practice, the working range is often from 10 nanograms per litre to 10 micrograms per litre.
Samples containing mercury at concentrations higher than the working range can be analysed following appropriate dilution of the sample. The method detection limit will be dependent on the selected operating conditions and calibration range. With high purity reagents, a method detection limit of less than 1 nanogram per litre is obtainable.The relative standard deviation is typically less than 5 % for concentrations greater than twenty times the method detection limit. The sensitivity of this method is dependent on the selected operating conditions.
Edition
1
Published Date
2006-05-22
Status
PUBLISHED
Pages
13
Format 
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Abstract
ISO 17852:2006 specifies a method for the determination of mercury in drinking, surface, ground and rain water using atomic fluorescence spectrometry. It may be applied to industrial and municipal waste water after an additional digestion step under appropriate conditions. The potential linear dynamic range is approximately 1 nanogram per litre to 100 micrograms per litre. In practice, the working range is often from 10 nanograms per litre to 10 micrograms per litre.
Samples containing mercury at concentrations higher than the working range can be analysed following appropriate dilution of the sample. The method detection limit will be dependent on the selected operating conditions and calibration range. With high purity reagents, a method detection limit of less than 1 nanogram per litre is obtainable.The relative standard deviation is typically less than 5 % for concentrations greater than twenty times the method detection limit. The sensitivity of this method is dependent on the selected operating conditions.
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