ISO 21438-2:2009

Workplace atmospheres — Determination of inorganic acids by ion chromatography — Part 2: Volatile acids, except hydrofluoric acid (hydrochloric acid, hydrobromic acid and nitric acid)

Workplace atmospheres — Determination of inorganic acids by ion chromatography — Part 2: Volatile acids, except hydrofluoric acid (hydrochloric acid, hydrobromic acid and nitric acid)

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Referenced standards

EN 13205ISO 1042ISO 3585ISO 648ISO 7708:1995ISO 8655-1ISO 8655-2ISO 8655-6ISO 8756
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ISO 21438-2:2009

Workplace atmospheres — Determination of inorganic acids by ion chromatography — Part 2: Volatile acids, except hydrofluoric acid (hydrochloric acid, hydrobromic acid and nitric acid)

Workplace atmospheres — Determination of inorganic acids by ion chromatography — Part 2: Volatile acids, except hydrofluoric acid (hydrochloric acid, hydrobromic acid and nitric acid)

ISO 21438-2:2009 specifies a method for the determination of the time-weighted average mass concentration of hydrogen chloride (HCl) gas and hydrochloric acid mist, hydrogen bromide (HBr) vapour and hydrobromic acid mist and nitric acid (HNO3) vapour and mist in workplace air by collection on an alkali-impregnated quartz fibre filter and analysis by ion chromatography.

For mist sampling, the method is applicable to the personal sampling of the inhalable fraction of airborne particles and to static (area) sampling.

The analytical method is applicable to the determination of masses of 0,01 mg to 2,5 mg of HCl, HBr and HNO3 per sample.

The range of concentrations of HCl, HBr and HNO3 in air for which the measuring procedure is applicable is determined by the sampling method selected by the user. For a 240-litre air sample, the working range is approximately 0,04 mg/m3 to 10 mg/m3 for HCl, HBr and HNO3.

The procedure is intended to differentiate between the acids and their corresponding salts. If both are present in the air, particulate salts are trapped on a pre-filter. Co-sampled particulate matter trapped on the pre-filter and/or deposited on the walls of the sampler may be analysed, if desired.

Acids can react with co-sampled particulate matter on the pre-filter, causing interference with the measurement of the acid concentration.

Edition2009
Standard Part No2
Published Date2009
Published ByInternational Standardization Organisation
Page Count29