A two-column method for long-term monitoring of non-methane hydrocarbons (NMHCs) and oxygenated volatile organic compounds (o-VOCs)

2002 ◽  
Vol 5 (1) ◽  
pp. 8-13 ◽  
Author(s):  
James R. Hopkins ◽  
Alastair C. Lewis ◽  
Katie A. Read
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Column Method ◽  
Oxygenated Volatile Organic Compounds ◽  
Volatile Organic ◽  
Long Term Monitoring ◽  
Term Monitoring

scholarly journals Development of a Water Matrix Certified Reference Material for Volatile Organic Compounds Analysis in Water

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4370
Author(s):  
Liping Fang ◽  
Linyan Huang ◽  
Gang Yang ◽  
Yang Jiang ◽  
Haiping Liu ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Reference Material ◽  
Organic Compounds ◽  
Certified Reference Material ◽  
Pure Water ◽  
Term Stability ◽  
Long Term Stability ◽  
Water Matrix ◽  
Volatile Organic

Water matrix certified reference material (MCRM) of volatile organic compounds (VOCs) is used to provide quality assurance and quality control (QA/QC) during the analysis of VOCs in water. In this research, a water MCRM of 28 VOCs was developed using a “reconstitution” approach by adding VOCs spiking, methanol solution into pure water immediately prior to analysis. The VOCs spiking solution was prepared gravimetrically by dividing 28 VOCs into seven groups, then based on ISO Guide 35, using gas chromatography-mass spectrometry (GC-MS) to investigate the homogeneity and long-term stability. The studies of homogeneity and long-term stability indicated that the batch of VOCs spiking solution was homogeneous and stable at room temperature for at least 15 months. Moreover, the water MCRM of 28 VOCs was certified by a network of nine competent laboratories, and the certified values and expanded uncertainties of 28 VOCs ranged from 6.2 to 17 μg/L and 0.5 to 5.3 μg/L, respectively.

scholarly journals Root anoxia effects on physiology and emissions of volatile organic compounds (VOC) under short- and long-term inundation of trees from Amazonian floodplains

SpringerPlus ◽  
2012 ◽  
Vol 1 (1) ◽  
pp. 9 ◽  
Author(s):  
Araceli Bracho-Nunez ◽  
Nina Knothe ◽  
Wallace R Costa ◽  
Liberato R Maria Astrid ◽  
Betina Kleiss ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Volatile Organic ◽  
Short And Long Term

scholarly journals Mapping Asian anthropogenic emissions of non-methane volatile organic compounds to multiple chemical mechanisms

2013 ◽  
Vol 13 (12) ◽  
pp. 32649-32701 ◽  
Author(s):  
M. Li ◽  
Q. Zhang ◽  
D. G. Streets ◽  
K. B. He ◽  
Y. F. Cheng ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Individual Species ◽  
Chemical Mechanisms ◽  
Mixing Ratios ◽  
Wide Range ◽  
Oxygenated Volatile Organic Compounds ◽  
Volatile Organic ◽  
Species Mapping ◽  
Multiple Chemical

Abstract. An accurate speciation mapping of non-methane volatile organic compounds (NMVOC) emissions has an important impact on the performance of chemical transport models (CTMs) in simulating ozone mixing ratios and secondary organic aerosols. In this work, we developed an improved speciation framework to generate model-ready anthropogenic Asian NMVOC emissions for various gas-phase chemical mechanisms commonly used in CTMs by using an explicit assignment approach and updated NMVOC profiles, based on the total NMVOC emissions in the INTEX-B Asian inventory for the year 2006. NMVOC profiles were selected and aggregated from a wide range of new measurements and the SPECIATE database. To reduce potential uncertainty from individual measurements, composite profiles were developed by grouping and averaging source profiles from the same category. The fractions of oxygenated volatile organic compounds (OVOC) were corrected during the compositing process for those profiles which used improper sampling and analyzing methods. Emissions of individual species were then lumped into species in different chemical mechanisms used in CTMs by applying mechanism-dependent species mapping tables, which overcomes the weakness of inaccurate mapping in previous studies. Gridded emissions for eight chemical mechanisms are developed at 30 min × 30 min resolution using various spatial proxies and are provided through the website: http://mic.greenresource.cn/intex-b2006. Emission estimates for individual NMVOC species differ between one and three orders of magnitude for some species when different sets of profiles are used, indicating that source profile is the most important source of uncertainties of individual species emissions. However, those differences are diminished in lumped species as a result of the lumping in the chemical mechanisms.

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.

Long-term soil biological fertility, volatile organic compounds and chemical properties in a vineyard soil after biochar amendment

Geoderma ◽  
2019 ◽  
Vol 344 ◽  
pp. 127-136 ◽  
Author(s):  
Laura Giagnoni ◽  
Anita Maienza ◽  
Silvia Baronti ◽  
Francesco Primo Vaccari ◽  
Lorenzo Genesio ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Chemical Properties ◽  
Volatile Organic ◽  
Vineyard Soil ◽  
Biochar Amendment ◽  
And Chemical Properties
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