scholarly journals Volatile organic compounds and ozone in Rocky Mountain National Park during FRAPPÉ

2019 ◽  
Vol 19 (1) ◽  
pp. 499-521 ◽  
Author(s):  
Katherine B. Benedict ◽  
Yong Zhou ◽  
Barkley C. Sive ◽  
Anthony J. Prenni ◽  
Kristi A. Gebhart ◽  
...  

Abstract. The 2014 Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) aimed to better characterize summertime air quality in the Northern Front Range Metropolitan Area (NFRMA) and its impact on surrounding areas. As part of this study, measurements of gas- and particle-phase species were collected in Rocky Mountain National Park (ROMO), located in the mountains west of the urban northern Front Range corridor from July to October 2014. We report on measurements of ozone from two locations in the park and a suite of volatile organic compounds (VOCs) measured using a continuous real-time gas chromatography (GC) system and a quadrupole proton-transfer-reaction mass spectrometer (PRT-MS) at the ROMO Longs Peak (ROMO-LP) air quality site. We also measured VOCs using canister samples collected along transects connecting the NFRMA and ROMO. These datasets show that ROMO is impacted by NFRMA emission sources, and high observed mixing ratios of VOCs associated with oil and gas extraction (e.g. ethane) and urban sources (e.g. ethene and C2Cl4) occur during periods of upslope transport. Hourly ozone mixing ratios exceeded 70 ppb during six events. Two of the six events were largely associated with VOCs from the oil and gas sector, three high ozone events were associated with a mixture of VOCs from urban and oil and gas sources, and one high ozone event was driven by a stratospheric intrusion. For the high ozone events most associated with emissions from oil and gas activities, we estimate that VOCs and NOx from sources along the Front Range contributed ∼20 ppbv of additional ozone.

2018 ◽  
Author(s):  
Katherine B. Benedict ◽  
Yong Zhou ◽  
Barkley C. Sive ◽  
Anthony J. Prenni ◽  
Kristi A. Gebhart ◽  
...  

Abstract. The 2014 Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) aimed to better characterize summertime air quality in the Northern Front Range Metropolitan Area (NFRMA) and its impact on surrounding areas. As part of this study, measurements of gas and particle phase species were collected in Rocky Mountain National Park (ROMO), located in the mountains west of the urban North Front Range corridor. We report on measurements of ozone from two locations in the park and a suite of volatile organic compounds (VOCs) measured using a continuous real-time gas chromatography system and a quadrupole proton-transfer reaction-mass spectrometer at the ROMO Longs Peak air quality site. We also measured VOCs using canister samples collected along transects connecting the NFRMA and ROMO. These datasets show that ROMO is impacted by NFRMA emission sources, and high observed mixing ratios of VOCs associated with oil and gas extraction (e.g. ethane) and urban sources (e.g. ethene and C2Cl4) occur during periods of upslope transport. Hourly ozone mixing ratios exceeded 70 ppb on six events. Two of the six events were largely associated with VOCs from the oil and gas sector, three high ozone events were associated with a mixture of VOCs from urban and oil and gas sources, and one high ozone event was driven by a stratospheric intrusion. For the high ozone events most associated with emissions from oil and gas activities, we estimate that VOCs from this sector contributed to ∼20 ppbv of additional ozone.


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.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4759 ◽  
Author(s):  
Katherine B. Benedict ◽  
Anthony J. Prenni ◽  
Amy P. Sullivan ◽  
Ashley R. Evanoski-Cole ◽  
Emily V. Fischer ◽  
...  

Human influenced atmospheric reactive nitrogen (RN) is impacting ecosystems in Rocky Mountain National Park (ROMO). Due to ROMO’s protected status as a Class 1 area, these changes are concerning, and improving our understanding of the contributions of different types of RN and their sources is important for reducing impacts in ROMO. In July–August 2014 the most comprehensive measurements (to date) of RN were made in ROMO during the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ). Measurements included peroxyacetyl nitrate (PAN), C1–C5alkyl nitrates, and high-time resolution NOx, NOy, and ammonia. A limited set of measurements was extended through October. Co-located measurements of a suite of volatile organic compounds provide information on source types impacting ROMO. Specifically, we use ethane as a tracer of oil and gas operations and tetrachloroethylene (C2Cl4) as an urban tracer to investigate their relationship with RN species and transport patterns. Results of this analysis suggest elevated RN concentrations are associated with emissions from oil and gas operations, which are frequently co-located with agricultural production and livestock feeding areas in the region, and from urban areas. There also are periods where RN at ROMO is impacted by long-range transport. We present an atmospheric RN budget and a nitrogen deposition budget with dry and wet components. Total deposition for the period (7/1–9/30) was estimated at 1.58 kg N/ha, with 87% from wet deposition during this period of above average precipitation. Ammonium wet deposition was the dominant contributor to total nitrogen deposition followed by nitrate wet deposition and total dry deposition. Ammonia was estimated to be the largest contributor to dry deposition followed by nitric acid and PAN (other species included alkyl nitrates, ammonium and nitrate). All three species are challenging to measure routinely, especially at high time resolution.


Atmosphere ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 286
Author(s):  
Dorina Camelia Ilieș ◽  
Florin Marcu ◽  
Tudor Caciora ◽  
Liliana Indrie ◽  
Alexandru Ilieș ◽  
...  

Poor air quality inside museums is one of the main causes influencing the state of conservation of exhibits. Even if they are mostly placed in a controlled environment because of their construction materials, the exhibits can be very vulnerable to the influence of the internal microclimate. As a consequence, museum exhibits must be protected from potential negative effects. In order to prevent and stop the process of damage of the exhibits, monitoring the main parameters of the microclimate (especially temperature, humidity, and brightness) and keeping them in strict values is extremely important. The present study refers to the investigations and analysis of air quality inside a museum, located in a heritage building, from Romania. The paper focuses on monitoring and analysing temperature of air and walls, relative humidity (RH), CO2, brightness and particulate matters (PM), formaldehyde (HCHO), and total volatile organic compounds (TVOC). The monitoring was carried out in the Summer–Autumn 2020 Campaign, in two different exhibition areas (first floor and basement) and the main warehouse where the exhibits are kept and restored. The analyses aimed both at highlighting the hazard induced by the poor air quality inside the museum that the exhibits face. The results show that this environment is potentially harmful to both exposed items and people. Therefore, the number of days in which the ideal conditions in terms of temperature and RH are met are quite few, the concentration of suspended particles, formaldehyde, and total volatile organic compounds often exceed the limit allowed by the international standards in force. The results represent the basis for the development and implementation of strategies for long-term conservation of exhibits and to ensure a clean environment for employees, restorers, and visitors.


Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 806
Author(s):  
Ozge Cemiloglu Ulker ◽  
Onur Ulker ◽  
Salim Hiziroglu

Volatile organic compounds (VOCs) are the main source influencing the overall air quality of an environment. It is a well-known fact that coated furniture units, in the form of paints and varnishes, emit VOCs, reducing the air quality and resulting in significant health problems. Exposure time to such compounds is also an important parameter regarding their possible health effects. Such issues also have a greater influence when the exposure period is extended. The main objective of this study was to review some of the important factors for the emission of VOCs from coated furniture, from the perspective of material characteristics, as well as health concerns. Some methods for controlling VOC emissions to improve indoor air quality, from the point of view recent regulations and suggestions, are also presented in this work.


2021 ◽  
Vol 13 (12) ◽  
pp. 6570
Author(s):  
Asma Akter Parlin ◽  
Monami Kondo ◽  
Noriaki Watanabe ◽  
Kengo Nakamura ◽  
Mizuki Yamada ◽  
...  

The quantitative understanding of the transport behavior of volatile organic compounds (VOCs) in near-surface soils is highly important in light of the potential impacts of soil VOC emissions on the air quality and climate. Previous studies have suggested that temperature changes affect the transport behavior; however, the effects are not well understood. Indeed, much larger changes in the VOC flux under in situ dynamic temperatures than those expected from the temperature dependence of the diffusion coefficients of VOCs in the air have been suggested but rarely investigated experimentally. Here, we present the results of a set of experiments on the upward vertical vapor-phase diffusive transport of benzene and trichloroethylene (TCE) in sandy soils with water contents ranging from an air-dried value to 10 wt% during sinusoidal temperature variation between 20 and 30 °C. In all experiments, the flux from the soil surface was correlated with the temperature, as expected. However, the changes in flux under wet conditions were unexpectedly large and increased with increasing water content; they were also larger for TCE, the volatility of which depended more strongly on the temperature. Additionally, the larger flux changes were accompanied by a recently discovered water-induced inverse correlation between temperature and flux into the overlying soil. These results demonstrated that the flux changes of VOCs under dynamic temperatures could be increased by volatilization-dissolution interactions of VOCs with water. Future extensive studies on this newly discovered phenomenon would contribute to a better understanding of the impacts of soil VOC emissions on the air quality and climate.


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