scholarly journals Non-radioactive Chemical Ionization Mass Spectrometry Using Acetic Acid–Acetate Cluster as a Reagent Ion for the Real-time Measurement of Acids and Hydroperoxides

2017 ◽  
Vol 46 (1) ◽  
pp. 38-41 ◽  
Author(s):  
Satoshi Inomata ◽  
Jun Hirokawa
2018 ◽  
Vol 11 (4) ◽  
pp. 1901-1920 ◽  
Author(s):  
Victoria Treadaway ◽  
Brian G. Heikes ◽  
Ashley S. McNeill ◽  
Indira K. C. Silwal ◽  
Daniel W. O'Sullivan

Abstract. A chemical ionization mass spectrometry (CIMS) method utilizing a reagent gas mixture of O2, CO2, and CH3I in N2 is described and optimized for quantitative gas-phase measurements of hydrogen peroxide (H2O2), methyl peroxide (CH3OOH), formic acid (HCOOH), and the sum of acetic acid (CH3COOH) and hydroxyacetaldehyde (HOCH2CHO; also known as glycolaldehyde). The instrumentation and methodology were designed for airborne in situ field measurements. The CIMS quantification of formic acid, acetic acid, and hydroxyacetaldehyde used I− cluster formation to produce and detect the ion clusters I−(HCOOH), I−(CH3COOH), and I−(HOCH2CHO), respectively. The CIMS also produced and detected I− clusters with hydrogen peroxide and methyl peroxide, I−(H2O2) and I−(CH3OOH), though the sensitivity was lower than with the O2− (CO2) and O2− ion clusters, respectively. For that reason, while the I− peroxide clusters are presented, the focus is on the organic acids. Acetic acid and hydroxyacetaldehyde were found to yield equivalent CIMS responses. They are exact isobaric compounds and indistinguishable in the CIMS used. Consequently, their combined signal is referred to as the acetic acid equivalent sum. Within the resolution of the quadrupole used in the CIMS (1 m∕z), ethanol and 1- and 2-propanol were potential isobaric interferences to the measurement of formic acid and the acetic acid equivalent sum, respectively. The CIMS response to ethanol was 3.3 % that of formic acid and the response to either 1- or 2-propanol was 1 % of the acetic acid response; therefore, the alcohols were not considered to be significant interferences to formic acid or the acetic acid equivalent sum. The multi-reagent ion system was successfully deployed during the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) in 2014. The combination of FRAPPÉ and laboratory calibrations allowed for the post-mission quantification of formic acid and the acetic acid equivalent sum observed during the Deep Convective Clouds and Chemistry Experiment in 2012.


2017 ◽  
Author(s):  
Victoria Treadaway ◽  
Brian G. Heikes ◽  
Ashley S. McNeill ◽  
Indiria K. C. Silwal ◽  
Daniel W. O'Sullivan

Abstract. A chemical ionization mass spectrometry (CIMS) method utilizing a reagent gas mixture of O2, CO2, and CH3I in N2 is described and optimized for quantitative gas-phase measurements of hydrogen peroxide (H2O2), methyl peroxide (CH3OOH), formic acid (HCOOH), and the sum of acetic acid (CH3COOH) and hydroxyacetaldehyde (HOCH2CHO; also known as glycolaldehyde). The instrumentation and methodology were designed for airborne in situ field measurements. The CIMS quantification of formic acid, acetic acid, and hydroxyacetaldehyde used I- cluster formation to produce and detect the ion clusters I (HCOOH), I (CH3COOH), and I (HOCH2CHO) respectively. Although hydrogen peroxide and methyl peroxide also form cluster ions with I-, the focus here is on the organic acids. Acetic acid and hydroxyacetaldehyde were found to yield equivalent CIMS responses. They are exact isobaric compounds and indistinguishable in the CIMS used. Consequently, their combined signal is referred to as "the acetic acid equivalent sum." Within the resolution of the quadrupole used in the CIMS (1 m/z), ethanol and 1- and 2-propanol were potential isobaric interferences to the measurement of formic acid and the acetic acid equivalent sum, respectively. The CIMS response to ethanol was 3.3 % that of formic acid and the response to either 1- or 2-propanol was 1 % of the acetic acid response; therefore, the alcohols were not considered to be significant interferences to acetic acid or the acetic acid equivalent sum. The multi-reagent ion system was successfully deployed during the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) in 2014. The combination of FRAPPÉ and laboratory calibrations allowed for the post-mission quantification of formic acid and the acetic acid equivalent sum observed during the Deep Convective Clouds and Chemistry Experiment in 2012.


2018 ◽  
Vol 11 (9) ◽  
pp. 5087-5104 ◽  
Author(s):  
Theodora Nah ◽  
Yi Ji ◽  
David J. Tanner ◽  
Hongyu Guo ◽  
Amy P. Sullivan ◽  
...  

Abstract. The sources and atmospheric chemistry of gas-phase organic acids are currently poorly understood, due in part to the limited range of measurement techniques available. In this work, we evaluated the use of SF6- as a sensitive and selective chemical ionization reagent ion for real-time measurements of gas-phase organic acids. Field measurements are made using chemical ionization mass spectrometry (CIMS) at a rural site in Yorkville, Georgia, from September to October 2016 to investigate the capability of this measurement technique. Our measurements demonstrate that SF6- can be used to measure a range of organic acids in the atmosphere. One-hour averaged ambient concentrations of organic acids ranged from a few parts per trillion by volume (ppt) to several parts per billion by volume (ppb). All the organic acids displayed similar strong diurnal behaviors, reaching maximum concentrations between 17:00 and 19:00 EDT. The organic acid concentrations are dependent on ambient temperature, with higher organic acid concentrations being measured during warmer periods.


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