TY - JOUR
T1 - Measurement of formic acid, acetic acid, formaldehyde and acetaldehyde in the atmosphere by ion chromatography
AU - Tanaka, Shigeru
AU - Iguchi, Masaru
AU - Yamanaka, Kazuo
AU - Yamada, Tomoyuki
AU - Nakao, Naoto
AU - Hashimoto, Yoshikazu
PY - 1987
Y1 - 1987
N2 - A method for the determination of formic acid, acetic acid, formaldehyde and acetaldehyde in the atmosphere by ion chromatography was investigated. These gases were collected by using two bubblers in series filled with 50 ml distilled water as a trapping solution. The collection efficiencies of the gases by this sampling system were almost 100% at an air flow rate 5 1/min for 4 h in the field measurement. Formic acid and acetic acid collected with distilled water were directly analyzed by ion chromatography. 0.005 M Na2B4O7 was suitable eluent for the ion chromatographic analysis of formate and acetate ions. It was possible to obtain good separation of formate and acetate ions and complete the analysis within 8 min by using 0.005 M Na2B4O7 eluent. Formaldehyde and acetaldehyde collected with distilled water could not be directly determined by ion chromatography with a conductimetric detector. It is therefore necessary to oxidize these aldehydes in the sample solution to formate and acetate for ion chromatographic analysis. The complete oxidation of formaldehyde and acetaldehyde to formate and acetate could be achieved by adding 5 ml of 1% H2O2 and 5 ml of 1 M NH4OH to a 40 ml sample solution, no loss of formate and acetate by the addition was observed. The concentration column was used for the analysis of samples at lower concentration levels. The relative standard deviations of 0.5 ppm formate and acetate determinations by the concentration column were 3~5%, and the detection limits were 0.005 ppm for formate and 0.01 ppm for acetate for a 5 ml injection volume. The measurements of the above gases in the atmosphere were done at two locations (Hiyoshi, Yokohama and Shiroganedai, Tokyo, from April to December, 1985) by using this method. The concentration range was l.5~7.5 μg/m3 for formic acid, 18.8~35.3 μg/m3 for acetic acid, 2.9~18 μg/m3 for formaldehyde and 5.3~ 18.8 μg/m3 for acetaldehyde, respectively. For a 1.2 m3 air sampling volume, the detection limits of this method were 0.2 μg/m3 for formic acid and formaldehyde and 0.4μg/m3 for acetic acid and acetaldehyde.
AB - A method for the determination of formic acid, acetic acid, formaldehyde and acetaldehyde in the atmosphere by ion chromatography was investigated. These gases were collected by using two bubblers in series filled with 50 ml distilled water as a trapping solution. The collection efficiencies of the gases by this sampling system were almost 100% at an air flow rate 5 1/min for 4 h in the field measurement. Formic acid and acetic acid collected with distilled water were directly analyzed by ion chromatography. 0.005 M Na2B4O7 was suitable eluent for the ion chromatographic analysis of formate and acetate ions. It was possible to obtain good separation of formate and acetate ions and complete the analysis within 8 min by using 0.005 M Na2B4O7 eluent. Formaldehyde and acetaldehyde collected with distilled water could not be directly determined by ion chromatography with a conductimetric detector. It is therefore necessary to oxidize these aldehydes in the sample solution to formate and acetate for ion chromatographic analysis. The complete oxidation of formaldehyde and acetaldehyde to formate and acetate could be achieved by adding 5 ml of 1% H2O2 and 5 ml of 1 M NH4OH to a 40 ml sample solution, no loss of formate and acetate by the addition was observed. The concentration column was used for the analysis of samples at lower concentration levels. The relative standard deviations of 0.5 ppm formate and acetate determinations by the concentration column were 3~5%, and the detection limits were 0.005 ppm for formate and 0.01 ppm for acetate for a 5 ml injection volume. The measurements of the above gases in the atmosphere were done at two locations (Hiyoshi, Yokohama and Shiroganedai, Tokyo, from April to December, 1985) by using this method. The concentration range was l.5~7.5 μg/m3 for formic acid, 18.8~35.3 μg/m3 for acetic acid, 2.9~18 μg/m3 for formaldehyde and 5.3~ 18.8 μg/m3 for acetaldehyde, respectively. For a 1.2 m3 air sampling volume, the detection limits of this method were 0.2 μg/m3 for formic acid and formaldehyde and 0.4μg/m3 for acetic acid and acetaldehyde.
KW - acetic acid
KW - collection by two bubblers in series contained with distilled water
KW - formaldehyde and acetaldehyde in the atmosphere
KW - ion chromatographic analysis of formate and acetate ions
KW - measurement of formic acid
KW - oxidation of aldehyde to carbonic acid by hydrogen peroxide
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U2 - 10.2116/bunsekikagaku.36.12
DO - 10.2116/bunsekikagaku.36.12
M3 - Article
AN - SCOPUS:84996013464
SN - 0525-1931
VL - 36
SP - 12
EP - 17
JO - Bunseki Kagaku
JF - Bunseki Kagaku
IS - 1
ER -