scholarly journals The Temporal and Spatial Distribution of Volatile Organic Compounds(VOCs) in the Urban Residential Atmosphere of Seoul, Korea

2010 ◽  
Vol 4 (1) ◽  
pp. 42-54 ◽  
Author(s):  
Ashish Anthwal ◽  
Chan-Goo Park ◽  
Kweon Jung ◽  
Min-Young Kim ◽  
Ki-Hyun Kim
2018 ◽  
Vol 7 (1) ◽  
pp. 373-388 ◽  
Author(s):  
Alejandro Moreno-Rangel ◽  
Tim Sharpe ◽  
Filbert Musau ◽  
Gráinne McGill

Abstract. Measurements of temporal and spatial changes to indoor contaminant concentrations are vital to understanding pollution characteristics. Whilst scientific instruments provide high temporal resolution of indoor pollutants, their cost and complexity make them unfeasible for large-scale projects. Low-cost monitors offer an opportunity to collect high-density temporal and spatial data in a broader range of households. This paper presents a user study to assess the precision, accuracy, and usability of a low-cost indoor air quality monitor in a residential environment to collect data about the indoor pollution. Temperature, relative humidity, total volatile organic compounds (tVOC), carbon dioxide (CO2) equivalents, and fine particulate matter (PM2.5) data were measured with five low-cost (“Foobot”) monitors and were compared with data from other monitors reported to be scientifically validated. The study found a significant agreement between the instruments with regard to temperature, relative humidity, total volatile organic compounds, and fine particulate matter data. Foobot CO2 equivalent was found to provide misleading CO2 levels as indicators of ventilation. Calibration equations were derived for tVOC, CO2, and PM2.5 to improve sensors' accuracy. The data were analysed based on the percentage of time pollutant levels that exceeded WHO thresholds. The performance of low-cost monitors to measure total volatile organic compounds and particulate matter 2.5 µm has not been properly addressed. The findings suggest that Foobot is sufficiently accurate for identifying high pollutant exposures with potential health risks and for providing data at high granularity and good potential for user or scientific applications due to remote data retrieval. It may also be well suited to remote and larger-scale studies in quantifying exposure to pollutants.


Chemosphere ◽  
2015 ◽  
Vol 134 ◽  
pp. 203-209 ◽  
Author(s):  
Katherine M. Mullaugh ◽  
Joanna M. Hamilton ◽  
G. Brooks Avery ◽  
J. David Felix ◽  
Ralph N. Mead ◽  
...  

2020 ◽  
Vol 149 ◽  
pp. 104311
Author(s):  
Dandan Huang ◽  
Mengxiao Sun ◽  
Mingzheng Han ◽  
Zihang Zhang ◽  
Yantao Miao ◽  
...  

2005 ◽  
Vol 48 (8) ◽  
pp. 1116-1131 ◽  
Author(s):  
Seong-Sook Park ◽  
Soon-Oh Kim ◽  
Seong-Taek Yun ◽  
Gi-Tak Chae ◽  
Soon-Young Yu ◽  
...  

Elem Sci Anth ◽  
2021 ◽  
Vol 9 (1) ◽  
Author(s):  
Samuel Rossabi ◽  
Jacques Hueber ◽  
Wei Wang ◽  
Pam Milmoe ◽  
Detlev Helmig

Methane and nonmethane volatile organic compounds (VOCs) were monitored near Boulder in the Northern Colorado Front Range to investigate their spatial distribution and sources as a part of the Front Range Air Pollution and Photochemistry Experiment (FRAPPE) and the Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) campaign, in summer 2014. A particular emphasis was the study of the contribution of emissions from oil and natural gas (O&NG) operations on the regional air quality. One network extended along an elevation gradient from the City of Boulder (elevation ≈1,600 m) to the University of Colorado Mountain Research Station (≈2900 m) on the eastern slopes of the Rocky Mountains. Light alkane petroleum hydrocarbons had the highest mole fraction of the VOCs that could be analyzed with the applied techniques. The longer lived VOCs ethane and propane decreased with increasing elevation, suggesting that Boulder and the surrounding plains were a source of these anthropogenic compounds. VOC diurnal time series showed a few events with elevated mole fractions at the mountain sites, which were likely the result of the upslope transport of plumes with elevated VOCs from the plains. Within the other site network, which extended into suburban East Boulder County (EBC), VOCs were monitored at 5 sites increasingly close to O&NG development in the Denver Julesburg Basin. Mean mole fractions and variability of primarily O&NG-associated VOCs (ethane, propane, butane isomers) increased by a factor of 2.4–5.2 with closer proximity to the O&NG producing region. Median mole fractions of C2–C5 n-alkanes and of imuch-butane at the EBC sites were higher than those previously reported from 28 larger urban areas in the United States. Among the VOCs that could be quantified with the gas chromatography methods, VOCs most clearly associated to O&NG-related emissions (C2–C5 alkanes) accounted for 52%–79% of the VOC hydroxyl radical reactivity (OHR). The horizontal gradient in OHR of the considered VOCs, with ≈3 times higher values at the furthest eastern sites, points toward higher chemical reactivity and ozone production potential from these ozone precursors in the eastern area of the county than within the City of Boulder.


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