TY - JOUR
T1 - Measurement of Parts per Million Level Gaseous Concentration of Hydrogen Sulfide by Ultraviolet Spectroscopy using 1,1,1,5,5,5-Hexafluoropentan-2,4-dione as a Derivative by Reaction of Cu(hfac)(1,5-Cyclooctadiene)
AU - Davidson, JM
AU - Pikramenou, Zoe
AU - Ponce, A
AU - Winpenny, REP
PY - 2009/5/1
Y1 - 2009/5/1
N2 - Hydrogen sulfide reacts rapidly and quantitatively at ppm levels with cycloocta-1,5-diene-1,1,1,5,5,5-hexafluoropentan-2,4-dionatocopper(I) (Cu(hfac)(COD)) to yield 1,1,1,5,5,5-hexafluoropentan-2,4-dione (Hhfac) having a strong ultraviolet absorption at 268 nm, and which can be used without interference as a derivative in the continuous, fast online spectroscopic determination of the H2S concentration. The analytical method has excellent selectivity and can be used in the presence of N2, H2, CO, COS, SO2, moist air, CH3OH, C2H4, C6H6, and light alkanes including fuel gases. Using a standard spectrometer, the level of detection is about 10 ppb. Concentrations down to 1 ppm H2S can be analyzed readily, usually with an error in the range 0 to −7% dependent largely on the sorption characteristics of the apparatus. These are systematic errors due to adsorption; however, the analytical apparatus was very stable, and relative standard deviations as low as 0.1% of the mean can be obtained. The method can also be applied to the analysis of methanethiol.
AB - Hydrogen sulfide reacts rapidly and quantitatively at ppm levels with cycloocta-1,5-diene-1,1,1,5,5,5-hexafluoropentan-2,4-dionatocopper(I) (Cu(hfac)(COD)) to yield 1,1,1,5,5,5-hexafluoropentan-2,4-dione (Hhfac) having a strong ultraviolet absorption at 268 nm, and which can be used without interference as a derivative in the continuous, fast online spectroscopic determination of the H2S concentration. The analytical method has excellent selectivity and can be used in the presence of N2, H2, CO, COS, SO2, moist air, CH3OH, C2H4, C6H6, and light alkanes including fuel gases. Using a standard spectrometer, the level of detection is about 10 ppb. Concentrations down to 1 ppm H2S can be analyzed readily, usually with an error in the range 0 to −7% dependent largely on the sorption characteristics of the apparatus. These are systematic errors due to adsorption; however, the analytical apparatus was very stable, and relative standard deviations as low as 0.1% of the mean can be obtained. The method can also be applied to the analysis of methanethiol.
UR - https://www.scopus.com/pages/publications/65649153041
U2 - 10.1021/ac9001035
DO - 10.1021/ac9001035
M3 - Article
C2 - 19361227
SN - 1520-6882
VL - 81
SP - 3669
EP - 3675
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 9
ER -