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Homepage>BS Standards>13 ENVIRONMENT. HEALTH PROTECTION. SAFETY>13.040 Air quality>13.040.30 Workplace atmospheres>BS ISO 16740:2005 Workplace air. Determination of hexavalent chromium in airborne particulate matter. Method by ion chromatography and spectrophotometric measurement using diphenyl carbazide
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immediate downloadReleased: 2005-02-24
BS ISO 16740:2005 Workplace air. Determination of hexavalent chromium in airborne particulate matter. Method by ion chromatography and spectrophotometric measurement using diphenyl carbazide

BS ISO 16740:2005

Workplace air. Determination of hexavalent chromium in airborne particulate matter. Method by ion chromatography and spectrophotometric measurement using diphenyl carbazide

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Standard number:BS ISO 16740:2005
Pages:50
Released:2005-02-24
ISBN:0 580 45558 0
Status:Standard
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BS ISO 16740:2005


This standard BS ISO 16740:2005 Workplace air. Determination of hexavalent chromium in airborne particulate matter. Method by ion chromatography and spectrophotometric measurement using diphenyl carbazide is classified in these ICS categories:
  • 13.040.30 Workplace atmospheres

This International Standard specifies a method for the determination of the time-weighted average mass concentration of hexavalent chromium in workplace air.

Separate sample preparation methods are specified for the extraction of soluble and insoluble hexavalent chromium. The method for insoluble hexavalent chromium can also be used to prepare samples for determination of total hexavalent chromium, if desired.

This International Standard is applicable to the personal sampling of the inhalable fraction of airborne particles, as defined in ISO 7708, and to static (area) sampling. The analytical method is applicable to the determination of masses of 0,01 µg to 10 µg of hexavalent chromium per sample, without dilution.

The concentration range of hexavalent chromium in air for which the measuring procedure is applicable is determined by the sampling method selected by the user (see 10.1). For a 1 m3 air sample, without sample dilution, the working range is approximately 0,01 µg·m−3 to 10 µg·m−3.