Proton-Transfer Chemical-Ionization Mass Spectrometry Allows Real-Time Analysis of Volatile Organic Compounds Released from Cutting and Drying of Crops

2000 ◽  
Vol 34 (12) ◽  
pp. 2640-2648 ◽  
Author(s):  
Joost A. de Gouw ◽  
Carleton J. Howard ◽  
Thomas G. Custer ◽  
Bradly M. Baker ◽  
Ray Fall
Keyword(s):  
Mass Spectrometry ◽  
Volatile Organic Compounds ◽  
Proton Transfer ◽  
Organic Compounds ◽  
Chemical Ionization ◽  
Chemical Ionization Mass Spectrometry ◽  
Ionization Mass ◽  
Time Analysis ◽  
Real Time Analysis ◽  
Volatile Organic

scholarly journals Using collision-induced dissociation to constrain sensitivity of ammonia chemical ionization mass spectrometry (NH<sub>4</sub><sup>+</sup> CIMS) to oxygenated volatile organic compounds

2019 ◽  
Vol 12 (3) ◽  
pp. 1861-1870 ◽  
Author(s):  
Alexander Zaytsev ◽  
Martin Breitenlechner ◽  
Abigail R. Koss ◽  
Christopher Y. Lim ◽  
James C. Rowe ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Mass Spectrometer ◽  
Chemical Ionization ◽  
Chemical Ionization Mass Spectrometry ◽  
Collision Induced Dissociation ◽  
Ionization Mass ◽  
Oxygenated Volatile Organic Compounds ◽  
Volatile Organic

Abstract. Chemical ionization mass spectrometry (CIMS) instruments routinely detect hundreds of oxidized organic compounds in the atmosphere. A major limitation of these instruments is the uncertainty in their sensitivity to many of the detected ions. We describe the development of a new high-resolution time-of-flight chemical ionization mass spectrometer that operates in one of two ionization modes: using either ammonium ion ligand-switching reactions such as for NH4+ CIMS or proton transfer reactions such as for proton-transfer-reaction mass spectrometer (PTR-MS). Switching between the modes can be done within 2 min. The NH4+ CIMS mode of the new instrument has sensitivities of up to 67 000 dcps ppbv−1 (duty-cycle-corrected ion counts per second per part per billion by volume) and detection limits between 1 and 60 pptv at 2σ for a 1 s integration time for numerous oxygenated volatile organic compounds. We present a mass spectrometric voltage scanning procedure based on collision-induced dissociation that allows us to determine the stability of ammonium-organic ions detected by the NH4+ CIMS instrument. Using this procedure, we can effectively constrain the sensitivity of the ammonia chemical ionization mass spectrometer to a wide range of detected oxidized volatile organic compounds for which no calibration standards exist. We demonstrate the application of this procedure by quantifying the composition of secondary organic aerosols in a series of laboratory experiments.

scholarly journals Development and validation of a portable gas phase standard generation and calibration system for volatile organic compounds

2010 ◽  
Vol 3 (3) ◽  
pp. 683-691 ◽  
Author(s):  
P. Veres ◽  
J. B. Gilman ◽  
J. M. Roberts ◽  
W. C. Kuster ◽  
C. Warneke ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Volatile Organic Compounds ◽  
Organic Carbon ◽  
Proton Transfer ◽  
Gas Phase ◽  
Organic Compounds ◽  
Total Carbon ◽  
Ionization Mass ◽  
Calibration System ◽  
Volatile Organic

Abstract. We report on the development of an accurate, portable, dynamic calibration system for volatile organic compounds (VOCs). The Mobile Organic Carbon Calibration System (MOCCS) combines the production of gas-phase VOC standards using permeation or diffusion sources with quantitative total organic carbon (TOC) conversion on a palladium surface to CO2 in the presence of oxygen, and the subsequent CO2 measurement. MOCCS was validated using three different comparisons: (1) TOC of high accuracy methane standards compared well to expected concentrations (3% relative error), (2) a gas-phase benzene standard was generated using a permeation source and measured by TOC and gas chromatography mass spectrometry (GC-MS) with excellent agreement (<4% relative difference), and (3) total carbon measurement of 4 known gas phase mixtures were performed and compared to a calculated carbon content to agreement within the stated uncertainties of the standards. Measurements from laboratory biomass burning experiments of formic acid by negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS) and formaldehyde by proton transfer reaction-mass spectrometry (PTR-MS), both calibrated using MOCCS, were compared to open path Fourier transform infrared spectroscopy (OP-FTIR) to validate the MOCCS calibration and were found to compare well (R2 of 0.91 and 0.99, respectively).

scholarly journals A high-resolution time-of-flight chemical ionization mass spectrometer utilizing hydronium ions (H<sub>3</sub>O<sup>+</sup> ToF-CIMS) for measurements of volatile organic compounds in the atmosphere

2016 ◽  
Vol 9 (6) ◽  
pp. 2735-2752 ◽  
Author(s):  
Bin Yuan ◽  
Abigail Koss ◽  
Carsten Warneke ◽  
Jessica B. Gilman ◽  
Brian M. Lerner ◽  
...  
Keyword(s):  
High Resolution ◽  
Volatile Organic Compounds ◽  
Proton Transfer ◽  
Organic Compounds ◽  
Chemical Ionization ◽  
Ionization Mass ◽  
Resolution Time ◽  
Hydronium Ions ◽  
Volatile Organic ◽  
Humidity Dependence

Abstract. Proton transfer reactions between hydronium ions (H3O+) and volatile organic compounds (VOCs) provide a fast and highly sensitive technique for VOC measurements, leading to extensive use of proton-transfer-reaction mass spectrometry (PTR-MS) in atmospheric research. Based on the same ionization approach, we describe the development of a high-resolution time-of-flight chemical ionization mass spectrometer (ToF-CIMS) utilizing H3O+ as the reagent ion. The new H3O+ ToF-CIMS has sensitivities of 100–1000 cps ppb−1 (ion counts per second per part-per-billion mixing ratio of VOC) and detection limits of 20–600 ppt at 3σ for a 1 s integration time for simultaneous measurements of many VOC species of atmospheric relevance. The ToF analyzer with mass resolution (m∕Δm) of up to 6000 allows the separation of isobaric masses, as shown in previous studies using similar ToF-MS. While radio frequency (RF)-only quadrupole ion guides provide better overall ion transmission than ion lens system, low-mass cutoff of RF-only quadrupole causes H3O+ ions to be transmitted less efficiently than heavier masses, which leads to unusual humidity dependence of reagent ions and difficulty obtaining a humidity-independent parameter for normalization. The humidity dependence of the instrument was characterized for various VOC species and the behaviors for different species can be explained by compound-specific properties that affect the ion chemistry (e.g., proton affinity and dipole moment). The new H3O+ ToF-CIMS was successfully deployed on the NOAA WP-3D research aircraft for the SONGNEX campaign in spring of 2015. The measured mixing ratios of several aromatics from the H3O+ ToF-CIMS agreed within ±10 % with independent gas chromatography measurements from whole air samples. Initial results from the SONGNEX measurements demonstrate that the H3O+ ToF-CIMS data set will be valuable for the identification and characterization of emissions from various sources, investigation of secondary formation of many photochemical organic products and therefore the chemical evolution of gas-phase organic carbon in the atmosphere.

scholarly journals Development and validation of a portable gas phase standard generation and calibration system for volatile organic compounds

2010 ◽  
Vol 3 (1) ◽  
pp. 333-357 ◽  
Author(s):  
P. Veres ◽  
J. B. Gilman ◽  
J. M. Roberts ◽  
W. C. Kuster ◽  
C. Warneke ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Volatile Organic Compounds ◽  
Organic Carbon ◽  
Proton Transfer ◽  
Gas Phase ◽  
Organic Compounds ◽  
Total Carbon ◽  
Ionization Mass ◽  
Calibration System ◽  
Volatile Organic

Abstract. We report on the development of an accurate, portable, dynamic calibration system for volatile organic compounds (VOCs). The Mobile Organic Carbon Calibration System (MOCCS) combines the production of gas-phase VOC standards using permeation or diffusion sources with quantitative total organic carbon (TOC) conversion on a palladium surface to CO2 in the presence of oxygen, and the subsequent CO2 measurement. MOCCS was validated using three different comparisons: (1) TOC of high accuracy methane standards compared well to expected concentrations (3% relative error), (2) a gas-phase benzene standard was generated using a permeation source and measured by TOC and gas chromatography mass spectrometry (GC-MS) with excellent agreement (<4% relative difference), and (3) total carbon measurement of 4 known gas phase mixtures were performed and compared to a calculated carbon content to agreement within the stated uncertainties of the standards. Measurements from laboratory biomass burning experiments of formic acid by negative-ion proton-transfer chemical-ionization mass spectrometry (NI-PT-CIMS) and formaldehyde by proton transfer reaction-mass spectrometry (PTR-MS), both calibrated using MOCCS, were compared to open path Fourier transform infrared spectroscopy (OP-FTIR) to validate the MOCCS calibration and were found to compare well (R2 of 0.91 and 0.99 respectively).

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