A versatile and uncomplicated method for the analysis of volatile organic compounds in ambient urban air

1999 ◽  
Vol 363 (4) ◽  
pp. 391-398 ◽  
Author(s):  
Markus Haider ◽  
H. Malissa
2016 ◽  
Author(s):  
B. Bonn ◽  
E. von Schneidemesser ◽  
D. Andrich ◽  
J. Quedenau ◽  
H. Gerwig ◽  
...  

Abstract. Urban air quality and human health are among the key aspects of future urban planning. In order to address pollutants such as ozone and particulate matter, efforts need to be made to quantify and reduce their concentrations. One important aspect in understanding urban air quality is the influence of urban vegetation which may act as both, emitter and sink for trace gases and aerosol particles. In this context, the "Berlin Air quality and Ecosystem Research: Local and long-range Impact of anthropogenic and Natural hydrocarbons 2014" (BAERLIN2014) campaign was conducted between the June 2nd and August 29th in the metropolitan area of Berlin-Brandenburg, Germany. The predominant goals of the campaign were (1) the characterization of urban gaseous and particulate pollution and its attribution to anthropogenic and natural sources in the region of interest, especially considering the connection between biogenic volatile organic compounds and particulates and ozone; (2) the quantification of the impact of urban vegetation on organic trace gas levels and the presence of oxidants such as ozone; and (3) to explain the local heterogeneity of pollutants by defining the distribution of sources and sinks relevant for the interpretation of model simulations. In order to do so, the campaign included stationary measurements at an urban background station and mobile observations carried out from bicycle, van and airborne platforms. This paper provides an overview of the mobile measurements (Mobile BAERLIN2014) and general conclusions drawn from the analysis. Bicycle measurements showed micro-scale variations of temperature and particulate matter, displaying a substantial reduction of temperature and particulates in the proximity of vegetated areas compared to typical urban residential area (background) measurements. Van measurements extended the area covered by bicycle observations and included continuous measurements of O3, NOx, CO, CO2, and pointwise volatile organic compounds (VOCs) identification. The quantification displayed notable horizontal heterogeneity of the short lived gases and particle number concentrations. E.g. concentrations of the traffic related chemical species CO and NO varied by more than ±20 % and ±60 % on the scale of one hundred meters, respectively. Airborne observations revealed the dominant source of elevated urban particulate number and mass concentrations being local, i.e. not being caused by long range transport. Surface based observations related these two parameters predominantly to traffic sources. Vegetated areas lowered the pollutant concentrations substantially with ozone being reduced most by coniferous forests, which is most likely caused by their reactive biogenic VOC emissions. With respect to the overall potential to reduce air pollutant levels forests were found to result in the largest decrease, followed by parks and facilities for sports and leisure. Surface temperature was generally 0.6–2.1 °C lower in vegetated regions, which in turn will have an impact on tropospheric chemical processes. Based on our findings effective future mitigation activities to provide a more sustainable and healthier urban environment would focus predominantly on reducing fossil-fuel emissions from traffic as well as on increasing vegetated areas.


Author(s):  
I. S. Denisov ◽  
V. V. Korotkov ◽  
D. S. Smirnov

For determining 22 volatile organic compounds in the atmospheric air, the operating modes of the gas chromatographic complexes «chromatography-mass spectrometer — two-stage thermodesorber» and «gas chromatograph with 2 FID — static headspace analysis sampler» are optimized. The modes provide the values of the separation coefficients of the chromatographic peaks in the range of 1.5 ÷ 21. It has been experimentally established that the highest desorption efficiency of volatile organic compounds is registered when the sample is concentrated into Tenax TA sorption tubes.


2016 ◽  
Author(s):  
Abigail R. Koss ◽  
Carsten Warneke ◽  
Bin Yuan ◽  
Matthew M. Coggon ◽  
Patrick R. Veres ◽  
...  

Abstract. NO+ chemical ionization mass spectrometry (NO+ CIMS) can achieve fast (sub 1-Hz) on-line measurement of trace atmospheric volatile organic compounds (VOCs) that cannot be ionized with H3O+ ions (e.g. in a PTR-MS or H3O+ CIMS instrument). Here we describe the adaptation of a high-resolution time-of-flight H3O+ CIMS instrument to use NO+ primary ion chemistry. We evaluate the NO+ technique with respect to compound specificity, sensitivity, and VOC species measured compared to H3O+. The evaluation is established by a series of experiments including laboratory investigation using a gas-chromatography (GC) interface, in-situ measurement of urban air using a GC interface, and direct in-situ measurement of urban air. The main findings are that (1) NO+ is useful for isomerically resolved measurements of carbonyl species; (2) NO+ can achieve sensitive detection of small (C4–C8) branched alkanes, but is not unambiguous for most; and (3) compound-specific measurement of some alkanes, especially iso-pentane, methylpentanes, and high mass (C12–C15) n-alkanes, is possible with NO+. We also demonstrate fast in-situ chemically specific measurements of C12 to C15 alkanes in ambient air.


1992 ◽  
Vol 26 (1) ◽  
pp. 165-173 ◽  
Author(s):  
Clyde W. Sweet ◽  
Stephen J. Vermette

2016 ◽  
Vol 16 (12) ◽  
pp. 7785-7811 ◽  
Author(s):  
Boris Bonn ◽  
Erika von Schneidemesser ◽  
Dorota Andrich ◽  
Jörn Quedenau ◽  
Holger Gerwig ◽  
...  

Abstract. Urban air quality and human health are among the key aspects of future urban planning. In order to address pollutants such as ozone and particulate matter, efforts need to be made to quantify and reduce their concentrations. One important aspect in understanding urban air quality is the influence of urban vegetation which may act as both emitter and sink for trace gases and aerosol particles. In this context, the "Berlin Air quality and Ecosystem Research: Local and long-range Impact of anthropogenic and Natural hydrocarbons 2014" (BAERLIN2014) campaign was conducted between 2 June and 29 August in the metropolitan area of Berlin and Brandenburg, Germany. The predominant goals of the campaign were (1) the characterization of urban gaseous and particulate pollution and its attribution to anthropogenic and natural sources in the region of interest, especially considering the connection between biogenic volatile organic compounds and particulates and ozone; (2) the quantification of the impact of urban vegetation on organic trace gas levels and the presence of oxidants such as ozone; and (3) to explain the local heterogeneity of pollutants by defining the distribution of sources and sinks relevant for the interpretation of model simulations. In order to do so, the campaign included stationary measurements at urban background station and mobile observations carried out from bicycle, van and airborne platforms. This paper provides an overview of the mobile measurements (Mobile BAERLIN2014) and general conclusions drawn from the analysis. Bicycle measurements showed micro-scale variations of temperature and particulate matter, displaying a substantial reduction of mean temperatures and particulate levels in the proximity of vegetated areas compared to typical urban residential area (background) measurements. Van measurements extended the area covered by bicycle observations and included continuous measurements of O3, NOx, CO, CO2 and point-wise measurement of volatile organic compounds (VOCs) at representative sites for traffic- and vegetation-affected sites. The quantification displayed notable horizontal heterogeneity of the short-lived gases and particle number concentrations. For example, baseline concentrations of the traffic-related chemical species CO and NO varied on average by up to ±22.2 and ±63.5 %, respectively, on the scale of 100 m around any measurement location. Airborne observations revealed the dominant source of elevated urban particulate number and mass concentrations being local, i.e., not being caused by long-range transport. Surface-based observations related these two parameters predominantly to traffic sources. Vegetated areas lowered the pollutant concentrations substantially with ozone being reduced most by coniferous forests, which is most likely caused by their reactive biogenic VOC emissions. With respect to the overall potential to reduce air pollutant levels, forests were found to result in the largest decrease, followed by parks and facilities for sports and leisure. Surface temperature was generally 0.6–2.1 °C lower in vegetated regions, which in turn will have an impact on tropospheric chemical processes. Based on our findings, effective future mitigation activities to provide a more sustainable and healthier urban environment should focus predominantly on reducing fossil-fuel emissions from traffic as well as on increasing vegetated areas.


2016 ◽  
Vol 9 (7) ◽  
pp. 2909-2925 ◽  
Author(s):  
Abigail R. Koss ◽  
Carsten Warneke ◽  
Bin Yuan ◽  
Matthew M. Coggon ◽  
Patrick R. Veres ◽  
...  

Abstract. NO+ chemical ionization mass spectrometry (NO+ CIMS) can achieve fast (1 Hz and faster) online measurement of trace atmospheric volatile organic compounds (VOCs) that cannot be ionized with H3O+ ions (e.g., in a PTR-MS or H3O+ CIMS instrument). Here we describe the adaptation of a high-resolution time-of-flight H3O+ CIMS instrument to use NO+ primary ion chemistry. We evaluate the NO+ technique with respect to compound specificity, sensitivity, and VOC species measured compared to H3O+. The evaluation is established by a series of experiments including laboratory investigation using a gas-chromatography (GC) interface, in situ measurement of urban air using a GC interface, and direct in situ measurement of urban air. The main findings are that (1) NO+ is useful for isomerically resolved measurements of carbonyl species; (2) NO+ can achieve sensitive detection of small (C4–C8) branched alkanes but is not unambiguous for most; and (3) compound-specific measurement of some alkanes, especially isopentane, methylpentane, and high-mass (C12–C15) n-alkanes, is possible with NO+. We also demonstrate fast in situ chemically specific measurements of C12 to C15 alkanes in ambient air.


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