scholarly journals Atmospheric aerosols in Rome, Italy: sources, dynamics and spatial variations during two seasons

2016 ◽  
Vol 16 (23) ◽  
pp. 15277-15299 ◽  
Author(s):  
Caroline Struckmeier ◽  
Frank Drewnick ◽  
Friederike Fachinger ◽  
Gian Paolo Gobbi ◽  
Stephan Borrmann
Keyword(s):  
Biomass Burning ◽  
Atmospheric Aerosols ◽  
Ground Level ◽  
Organic Aerosol ◽  
Saharan Dust ◽  
Urban Site ◽  
Temporal Behaviour ◽  
Urban Location ◽  
Polycyclic Aromatic ◽  
Primary Emissions

Abstract. Investigations on atmospheric aerosols and their sources were carried out in October/November 2013 and May/June 2014 consecutively in a suburban area of Rome (Tor Vergata) and in central Rome (near St Peter's Basilica). During both years a Saharan dust advection event temporarily increased PM10 concentrations at ground level by about 12–17 µg m−3. Generally, in October/November the ambient aerosol was more strongly influenced by primary emissions, whereas higher relative contributions of secondary particles (sulfate, aged organic aerosol) were found in May/June. Absolute concentrations of anthropogenic emission tracers (e.g. NOx, CO2, particulate polycyclic aromatic hydrocarbons, traffic-related organic aerosol) were generally higher at the urban location. Positive matrix factorization was applied to the PM1 organic aerosol (OA) fraction of aerosol mass spectrometer (HR-ToF-AMS) data to identify different sources of primary OA (POA): traffic, cooking, biomass burning and (local) cigarette smoking. While biomass burning OA was only found at the suburban site, where it accounted for the major fraction of POA (18–24 % of total OA), traffic and cooking were more dominant sources at the urban site. A particle type associated with cigarette smoke emissions, which is associated with a potential characteristic marker peak (m∕z 84, C5H10N+, a nicotine fragment) in the mass spectrum, was only found in central Rome, where it was emitted in close vicinity to the measurement location. Regarding secondary OA, in October/November, only a very aged, regionally advected oxygenated OA was found, which contributed 42–53 % to the total OA. In May/June total oxygenated OA accounted for 56–76 % of the OA. Here a fraction (18–26 % of total OA) of a fresher, less oxygenated OA of more local origin was also observed. New particle formation events were identified from measured particle number concentrations and size distributions in May/June 2014 at both sites. While they were observed every day at the urban location, at the suburban location they were only found under favourable meteorological conditions, but were independent of advection of the Rome emission plume. Particles from sources in the metropolitan area of Rome and particles advected from outside Rome contributed 42–70 and 30–58 % to the total measured PM1, respectively. Apart from the general aerosol characteristics, in this study the properties (e.g. emission strength) and dynamics (e.g. temporal behaviour) of each identified aerosol type is investigated in detail to provide a better understanding of the observed seasonal and spatial differences.

scholarly journals Atmospheric aerosols in Rome, Italy: Sources, dynamics and spatial variations during two seasons

2016 ◽  
Author(s):  
Caroline Struckmeier ◽  
Frank Drewnick ◽  
Friederike Fachinger ◽  
Gian Paolo Gobbi ◽  
Stephan Borrmann
Keyword(s):  
Biomass Burning ◽  
Atmospheric Aerosols ◽  
Polyaromatic Hydrocarbons ◽  
Ground Level ◽  
Organic Aerosol ◽  
Saharan Dust ◽  
Urban Site ◽  
Temporal Behaviour ◽  
Urban Location ◽  
Primary Emissions

Abstract. Investigations on atmospheric aerosols and their sources were performed during October/November 2013 and May/June 2014 subsequently in a suburban area of Rome (Tor Vergata) and in central Rome (near St. Peter's Basilica). During both years a Saharan dust advection event temporarily increased PM10 concentrations at ground level by approximately 10 µg m−3. Generally, during Oct/Nov the ambient aerosol was more strongly influenced by primary emissions, whereas higher relative contributions of secondary particles (sulphate, aged organic aerosol) were found during May/June. Absolute concentrations of anthropogenic emission tracers (e.g. NOx, CO2, particulate polyaromatic hydrocarbons, traffic-related organic aerosol) were generally higher at the urban location. Positive matrix factorisation was applied to the PM1 organic aerosol (OA) fraction of aerosol mass spectrometer (HR-ToF-AMS) data in order to identify different sources of primary OA (POA): traffic, cooking, biomass burning, and (local) cigarette smoking. While biomass burning OA was only found at the suburban site, where it accounted for the major fraction of POA (18–24 % of total OA), traffic and cooking were more dominant sources at the urban site. A particle type associated with cigarette smoke emissions, which is associated with a potential characteristic marker peak (m/z 84, C5H10N+, a nicotine fragment) in the mass spectrum, was only found in central Rome, where it was emitted in close vicinity to the measurement location. Regarding secondary OA, in Oct/Nov, only a very aged, regionally advected oxygenated OA was found, which contributed 42–53 % to the total OA. In May/June total oxygenated OA accounted for 56–76 % of the OA. Here also a fraction (18–26 % of total OA) of a fresher, less oxygenated OA of more local origin was observed. New particle formation events were identified from measured particle number concentrations and size distributions during May/June 2014 at both sites. While they were observed every day at the urban location, at the suburban location they were only found under favourable meteorological conditions, but independent of advection of the Rome emission plume. Particles from sources in the metropolitan area of Rome and particles advected from outside Rome contributed 42–70 % and 30–58 % to total measured PM1, respectively. Apart from the general aerosol characteristics, in this study the properties (e.g. emission strength) and dynamics (e.g. temporal behaviour) of each identified aerosol type is investigated in detail in order to provide a better understanding of the observed seasonal and spatial differences.

scholarly journals Sources of water-soluble Brown Carbon at a South-Eastern European Site

2021 ◽  
Author(s):  
Charalampia Baliaka ◽  
Christos Kaltsonoudis ◽  
Kalliopi Florou ◽  
Spiro Jorga ◽  
Christina Vasilakopoulou ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Light Absorption ◽  
Organic Aerosol ◽  
Water Soluble ◽  
Automated System ◽  
Urban Site ◽  
Multiple Sources ◽  
Brown Carbon ◽  
Liquid Waveguide Capillary Cell ◽  
Primary Emissions

<p>Atmospheric brown carbon (BrC) is a highly uncertain, but potentially important contributor to light absorption in the atmosphere. Laboratory and field studies have shown that BrC can be produced from multiple sources, including primary emissions from fossil fuel combustion and biomass burning (BB), as well as secondary formation through a number of reaction pathways. It is currently thought that the dominant source of atmospheric BrC is primary emissions from BB, but relatively few studies demonstrate this in environments with complex source profiles.</p><p>A field campaign was conducted during a month-long wintertime period in 2020 on the campus of the University of Peloponnese in the southwest of Patras, Greece which represents an urban site. During this time, ambient filter samples (a total of 35 filters) were collected from which the water-soluble BrC was determined using a semi-automated system similar to Hecobian et al. (2010),  where absorption was measured over a 1 m path length. To measure the BrC, a UV-Vis Spectrophotometer was coupled to a Liquid Waveguide Capillary Cell and the light absorption intensity was recorded at 365 and 700 nm. The latter was used as a reference wavelength. We found that the average BrC absorption in Patras at a wavelength of 365 nm was 8.5 ± 3.9 Mm<sup>-1</sup> suggesting that there was significant BrC in the organic aerosol during this period. Attribution of sources of BrC was done using simultaneous chemical composition data observations (primarily organic carbon, black carbon, and nitrate) combined with Positive Matrix Factorization analysis. This analysis showed that in addition to the important role of biomass burning (a contribution of about 20%) and other combustion emissions (also close to 20%), oxidized organic aerosol (approximately 40%) is also a significant contributor to BrC in the study area.</p><p><strong>Reference</strong></p><p>Hecobian, A., Zhang, X., Zheng, M., Frank, N., Edgerton, E.S., Weber, R.J., 2010. Water-soluble organic aerosol material and the light-absorption characteristics of aqueous extracts measured over the Southeastern United States. Atmos. Chem. Phys. 10, 5965–5977. https://doi.org/10.5194/acp-10-5965-2010</p><p> </p>

scholarly journals The impact of biomass burning and aqueous-phase processing on air quality: a multi-year source apportionment study in the Po Valley, Italy

2019 ◽  
Author(s):  
Marco Paglione ◽  
Stefania Gilardoni ◽  
Matteo Rinaldi ◽  
Stefano Decesari ◽  
Nicola Zanca ◽  
...  
Keyword(s):  
Air Quality ◽  
Source Apportionment ◽  
Biomass Burning ◽  
Organic Aerosol ◽  
Cold Season ◽  
World Health ◽  
Rural Site ◽  
Urban Site ◽  
Urban Background ◽  
Po Valley

Abstract. The Po Valley (Italy) is a well-known air quality hotspot characterized by Particulate Matter (PM) levels well above the limit set by the European Air Quality Directive and by the World Health Organization, especially during the colder season. In the framework of the Emilia-Romagna regional project SUPERSITO, the southern Po Valley submicron aerosol chemical composition was characterized by means of High-Resolution Aerosol Mass Spectroscopy (HR-AMS) with the specific aim of organic aerosol (OA) characterization and source apportionment. Eight intensive observation periods (IOPs) were carried out over four years (from 2011 to 2014) at two different sites (Bologna, BO, urban background and San Pietro Capofiume, SPC, rural background), to characterize the spatial variability and seasonality of the OA sources, with a special focus on the cold season. On the multi-year basis of the study, the AMS observations show that OA accounts for an average 45 ± 8 % (ranging 33–58 %) and 46 ± 7 % (ranging 36–50 %) of the total non-refractory submicron particle mass (PM1-NR) at the urban and at the rural site, respectively. Primary organic aerosol (POA) comprises biomass burning (23 ± 13 % of OA) and fossil fuel (12 ± 7 %) contributions with a marked seasonality in concentration. As expected, the biomass burning contribution to POA is more significant at the rural site (urban/rural concentrations ratio of 0.67), but it is also an important source of POA at the urban site during the cold season, with contributions ranging from 14 to 38 % of the total OA mass. Secondary organic aerosol (SOA) contribute to OA mass to a much larger extent than POA at both sites throughout the year (69 ± 16 % and 83 ± 16 % at urban and rural, respectively), with important implications for public health. Within the secondary fraction of OA, the measurements highlight the importance of biomass burning ageing products during the cold season, even at the urban background site. This biomass burning SOA fraction represents 14–44 % of the total OA mass in the cold season, indicating that in this region a major contribution of combustion sources to PM mass is mediated by environmental conditions and atmospheric reactivity. Among the environmental factors controlling the formation of SOA in the Po Valley, the availability of liquid water in the aerosol was shown to play a key role in the cold season. We estimate that organic fraction originating from aqueous reactions of biomass burning products (bb-aqSOA) represents 21 % (14–28 %) and 25 % (14–35 %) of the total OA mass and 44 % (32–56 %) and 61 % (21–100 %) of the SOA mass at the urban and rural sites, respectively.

scholarly journals Detection of Saharan dust and biomass burning events using near real-time intensive aerosol optical properties in the northwestern Mediterranean

2016 ◽  
Author(s):  
M. Ealo ◽  
A. Alastuey ◽  
A. Ripoll ◽  
N. Pérez ◽  
M. C. Minguillón ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Mineral Dust ◽  
Organic Aerosol ◽  
Saharan Dust ◽  
Aerosol Optical Properties ◽  
Angstrom Exponent ◽  
Ångström Exponent ◽  
Dust Events ◽  
Ångstrom Exponent

Abstract. The study of Saharan dust events (SDE) and biomass burning (BB) emissions are both topic of great scientific interest since they are frequent and important polluting scenarios affecting air quality and climate. The main aim of this work is evaluating the feasibility of using near real-time in situ aerosol optical measurements for the detection of these atmospheric events in the Western Mediterranean Basin (WMB). With this aim, intensive aerosol optical properties (SAE: scattering Ångström exponent, AAE: absorption Ångström exponent, SSAAE: single scattering albedo Ångström exponent, and g: asymmetry parameter) were derived from multi-wavelength aerosol light scattering, hemispheric backscattering and absorption measurements performed at regional (Montseny; MSY, 720 m a.s.l.) and continental (Montsec; MSA, 1570 m a.s.l.) background sites in the WMB. A sensitivity study aiming at calibrating the measured intensive optical properties for SDE and BB detection is presented and discussed. The detection of Saharan dust events (SDE) by means of the SSAAE parameter and Ångström matrix depended on the altitude of the measurement station, and on SDE intensity. At MSA (mountain-top site) SSAAE detected around 85% of SDE compared with 50% at MSY station, where pollution episodes dominated by fine anthropogenic particles frequently masked the effect of mineral dust on optical properties during less intense SDE. Furthermore, an interesting feature of SSAAE was its capability to detect the presence of mineral dust after the end of SDE. Thus, resuspension processes driven by summer regional atmospheric circulations and dry conditions after SDE favored the accumulation of mineral dust at regional level having important consequences for air quality. On average, SAE, AAE and g ranged between -0.7 and 1, 1.3 and 2.5, and 0.5 and 0.75, respectively, during SDE. Based on the Aethalometer model, biomass burning (BB) contribution to equivalent black carbon (BC) accounted for 36% and 40% at MSY and MSA respectively. Linear relationships were found between AAE and %BCbb, with AAE values reaching around 1.5 when %BCbb was higher than 50%. BB contribution to organic matter (OM) at MSY was around 30%. Thus FF combustion sources showed important contributions to both BC and OM in the region under study. Results for OM source apportionment showed good agreement with simultaneous biomass burning organic aerosol (BBOA) and hydrocarbon-like organic aerosol (HOA) calculated from Positive Matrix Factorization (PMF) applied to simultaneous Aerosol Mass Spectrometer (ACSM) measurements. A wildfire episode was identified at MSY, showing AAE values up to 2 when daily BB contributions to BC and OM were 73% and 78% respectively.

scholarly journals Regional influence of wildfires on aerosol chemistry in the western US and insights into atmospheric aging of biomass burning organic aerosol

2017 ◽  
Vol 17 (3) ◽  
pp. 2477-2493 ◽  
Author(s):  
Shan Zhou ◽  
Sonya Collier ◽  
Daniel A. Jaffe ◽  
Nicole L. Briggs ◽  
Jonathan Hee ◽  
...  
Keyword(s):  
Pacific Northwest ◽  
Chemical Transformation ◽  
Biomass Burning ◽  
Atmospheric Aerosols ◽  
Global Climate ◽  
Organic Aerosol ◽  
The United States ◽  
Aerosol Composition ◽  
Western Us ◽  
The Impact

Abstract. Biomass burning (BB) is one of the most important contributors to atmospheric aerosols on a global scale, and wildfires are a large source of emissions that impact regional air quality and global climate. As part of the Biomass Burning Observation Project (BBOP) field campaign in summer 2013, we deployed a high-resolution time-of-flight aerosol mass spectrometer (HR-AMS) coupled with a thermodenuder at the Mt. Bachelor Observatory (MBO, ∼  2.8 km above sea level) to characterize the impact of wildfire emissions on aerosol loading and properties in the Pacific Northwest region of the United States. MBO represents a remote background site in the western US, and it is frequently influenced by transported wildfire plumes during summer. Very clean conditions were observed at this site during periods without BB influence where the 5 min average (±1σ) concentration of non-refractory submicron aerosols (NR-PM1) was 3.7 ± 4.2 µg m−3. Aerosol concentration increased substantially (reaching up to 210 µg m−3 of NR-PM1) for periods impacted by transported BB plumes, and aerosol composition was overwhelmingly organic. Based on positive matrix factorization (PMF) of the HR-AMS data, three types of BB organic aerosol (BBOA) were identified, including a fresh, semivolatile BBOA-1 (O ∕ C  =  0.35; 20 % of OA mass) that correlated well with ammonium nitrate; an intermediately oxidized BBOA-2 (O ∕ C  =  0.60; 17 % of OA mass); and a highly oxidized BBOA-3 (O ∕ C  =  1.06; 31 % of OA mass) that showed very low volatility with only  ∼  40 % mass loss at 200 °C. The remaining 32 % of the OA mass was attributed to a boundary layer (BL) oxygenated OA (BL-OOA; O ∕ C  =  0.69) representing OA influenced by BL dynamics and a low-volatility oxygenated OA (LV-OOA; O ∕ C  =  1.09) representing regional aerosols in the free troposphere. The mass spectrum of BBOA-3 resembled that of LV-OOA and had negligible contributions from the HR-AMS BB tracer ions – C2H4O2+ (m∕z = 60.021) and C3H5O2+ (m∕z = 73.029); nevertheless, it was unambiguously related to wildfire emissions. This finding highlights the possibility that the influence of BB emission could be underestimated in regional air masses where highly oxidized BBOA (e.g., BBOA-3) might be a significant aerosol component but where primary BBOA tracers, such as levoglucosan, are depleted. We also examined OA chemical evolution for persistent BB plume events originating from a single fire source and found that longer solar radiation led to higher mass fraction of the chemically aged BBOA-2 and BBOA-3 and more oxidized aerosol. However, an analysis of the enhancement ratios of OA relative to CO (ΔOA ∕ΔCO) showed little difference between BB plumes transported primarily at night versus during the day, despite evidence of substantial chemical transformation in OA induced by photooxidation. These results indicate negligible net OA production in photochemically aged wildfire plumes observed in this study, for which a possible reason is that SOA formation was almost entirely balanced by BBOA volatilization. Nevertheless, the formation and chemical transformation of BBOA during atmospheric transport can significantly influence downwind sites with important implications for health and climate.

scholarly journals Organic aerosol volatility and viscosity in North China Plain: Contrast between summer and winter

2020 ◽  
Author(s):  
Weiqi Xu ◽  
Chun Chen ◽  
Yanmei Qiu ◽  
Ying Li ◽  
Zhiqiang Zhang ◽  
...  
Keyword(s):  
Coal Combustion ◽  
North China Plain ◽  
North China ◽  
Organic Aerosol ◽  
Rural Site ◽  
Urban Site ◽  
Aerosol Mass ◽  
Effective Saturation ◽  
Formation And Evolution ◽  
Primary Emissions

Abstract. Volatility and viscosity have substantial impacts on gas-particle partitioning, formation and evolution of aerosol, and hence the predictions of aerosol related air quality and climate effects. Here aerosol volatility and viscosity at a rural site (Gucheng) and an urban site (Beijing) in North China Plain (NCP) in summer and winter were investigated by using a thermodenuder coupled with high resolution aerosol mass spectrometer. The effective saturation concentration (C*) of organic aerosol (OA) in summer was smaller than that in winter (0.55 μg m−3 vs. 0.71–0.75 μg m−3), indicating that OA in winter in NCP is more volatile due to enhanced primary emissions from coal combustion and biomass burning. The volatility distributions varied largely different among different OA factors. In particular, we found that hydrocarbon-like OA (HOA) contained more non-volatile compounds compared to coal combustion related OA. The more oxidized oxygenated OA (MO-OOA) showed overall lower volatility than less oxidized OOA (LO-OOA) in both summer and winter, yet the volatility of MO-OOA was found to be relative humidity (RH) dependent showing more volatile properties at higher RH. Our results demonstrated the different composition and chemical formation pathways of MO-OOA under different RH levels. The glass transition temperature (Tg) and viscosity of OA in summer and winter are estimated using the recently developed parameterization formula. Our results showed that the Tg of OA in summer in Beijing (291.5 K) was higher than that in winter (289.7–290.0 K), while it varied greatly among different OA factors. The viscosity suggested that OA existed mainly as solid in winter in Beijing, but as semi-solids in Beijing in summer and Gucheng in winter. These results have important implications that kinetically limited gas-particle partitioning may need to be considered when simulating secondary OA formation in NCP.

scholarly journals Temperature-induced volatility of molecular markers in ambient airborne particulate matter

2010 ◽  
Vol 10 (8) ◽  
pp. 20329-20353
Author(s):  
C. R. Ruehl ◽  
W. A. Ham ◽  
M. J. Kleeman
Keyword(s):  
Molecular Markers ◽  
Particulate Matter ◽  
Airborne Particulate Matter ◽  
Organic Aerosol ◽  
Urban Site ◽  
Atmospheric Conditions ◽  
Ambient Conditions ◽  
Aerosol Mass ◽  
Polycyclic Aromatic ◽  
Effective Saturation

Abstract. Molecular markers are organic compounds used to represent known sources of particulate matter (PM) in statistical source apportionment studies. The utility of molecular markers depends on, among other things, their ability to represent PM volatility under realistic atmospheric conditions. We measured the particle-phase concentrations and temperature-induced volatility of commonly-used molecular markers in California's heavily polluted San Joaqin Valley. Concentrations of elemental carbon, organic carbon, levoglucosan, and polycyclic aromatic hydrocarbons were not reduced by mild (~10 K) heating. In contrast, both hopane/sterane and n-alkane concentrations were reduced, especially during the summer sampling events at the urban site. These results suggest that hopanes and steranes have effective saturation concentrations ~1 μg m−3, and therefore can be considered semi-volatile in realistic ambient conditions. The volatility behavior of n-alkanes during the urban summer is consistent with that predicted for absorption by suberic acid (a C8 diacid) using a group contribution modelling method. Observations can also be matched by an absorbent whose composition is based on recently-obtained high-resolution aerosol mass spectrometer factors (approximately 33% "hydrocarbon-like" and 67% oxygenated organic aerosol). The diminished volatility of the n-alkanes, hopanes, and steranes during rural and/or winter experiments could be explained by a more oxygenated absorbing phase along with a non-absorptive partitioning mechanism, such as adsorption to soot. This suggests that the temperature-induced volatility of large hydrocarbons in PM is most important if a relatively non-polar absorbing organic phase exists. While the activity coefficients of most organic aerosol compounds may be close to unity, the assumption of ideality for large hydrocarbons (e.g., hopanes) may result in large errors in partitioning calculations.

scholarly journals Regional Influence of Wildfires on Aerosol Chemistry in the Western US and Insights into Atmospheric Aging of Biomass Burning Organic Aerosol

2016 ◽  
Author(s):  
Shan Zhou ◽  
Sonya Collier ◽  
Daniel A. Jaffe ◽  
Nicole L. Briggs ◽  
Jonathan Hee ◽  
...  
Keyword(s):  
Pacific Northwest ◽  
Biomass Burning ◽  
Atmospheric Aerosols ◽  
Global Climate ◽  
Organic Aerosol ◽  
The United States ◽  
Global Scale ◽  
Aerosol Composition ◽  
Photo Oxidation ◽  
The Impact

Abstract. Biomass burning (BB) is one of the most important contributors to atmospheric aerosols on a global scale and wildfires are a large source of emissions that impact regional air quality and global climate. As part of the Biomass Burning Observation Project (BBOP) field campaign in summer 2013, we deployed a High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-AMS) coupled with a thermodenuder at the Mt. Bachelor Observatory (MBO, ~ 2.8 km above sea level) to characterize the impact of wildfire emissions on aerosol loading and properties in the Pacific Northwest region of the United States. MBO represents a remote background site in the western U.S. and it is frequently influenced by transported wildfire plumes during summer. Very clean conditions were observed at this site during periods without BB influence where the 5-min average (±1σ) concentration of non-refractory submicron aerosols (NR-PM1) was 3.7 ± 4.2 μg m−3. Aerosol concentration increased substantially (reaching up to 210 µg m−3 of NR-PM1) for periods impacted by transported BB plumes and aerosol composition was overwhelmingly organic. Based on Positive Matrix Factorization (PMF) of the HR-AMS data, three types of BB organic aerosol (BBOA) were identified, including a fresh, semivolatile BBOA-1 (O/C = 0.35; 20 % of OA mass) that correlated well with ammonium nitrate, an intermediately oxidized BBOA-2 (O/C = 0.60; 17 % of OA mass), and a highly oxidized BBOA-3 (O/C = 1.06; 31 % of OA mass) that showed very low volatility with only ~ 40 % mass loss at 200 °C. The remaining 32 % of the organic aerosol (OA) mass was attributed to a boundary layer (BL) OOA (BL-OOA; O/C = 0.69) representing OA influenced by BL dynamics and a low-volatility oxygenated OA (LV-OOA; O/C = 1.09) representing regional free troposphere aerosol. The mass spectrum of BBOA-3 resembled that of LV-OOA and had negligible contributions from the HR-AMS BB tracer ions – C2H4O2+ (m/z = 60.021) and C3H5O2+ (m/z = 73.029). This finding highlights the possibility that the influence of BB emission could be underestimated in regional air masses where highly oxidized BBOA (e.g. BBOA-3) might be a significant aerosol component. We also examined OA chemical evolution for persistent BB plume events originating from a single fire source and found that longer solar radiation led to higher mass fraction of the chemically aged BBOA-2 and BBOA-3 and more oxidized aerosol. However, an analysis of the enhancement ratios of OA relative to CO (ΔOA/ΔCO) showed little difference between BB plumes transported primarily at night versus during the day, despite evidence of substantial chemical transformation in OA induced by photo-oxidation. These results indicate negligible net OA production with photo-oxidation for wildfire plumes observed in this study, for which a possible reason is that SOA formation was almost entirely balanced by BBOA volatilization.

scholarly journals The impact of biomass burning and aqueous-phase processing on air quality: a multi-year source apportionment study in the Po Valley, Italy

2020 ◽  
Vol 20 (3) ◽  
pp. 1233-1254 ◽  
Author(s):  
Marco Paglione ◽  
Stefania Gilardoni ◽  
Matteo Rinaldi ◽  
Stefano Decesari ◽  
Nicola Zanca ◽  
...  
Keyword(s):  
Air Quality ◽  
Source Apportionment ◽  
Biomass Burning ◽  
Organic Aerosol ◽  
Cold Season ◽  
Rural Site ◽  
Urban Site ◽  
Urban Background ◽  
Po Valley ◽  
Rural Sites

Abstract. The Po Valley (Italy) is a well-known air quality hotspot characterized by particulate matter (PM) levels well above the limit set by the European Air Quality Directive and by the World Health Organization, especially during the colder season. In the framework of Emilia-Romagna regional project “Supersito”, the southern Po Valley submicron aerosol chemical composition was characterized by means of high-resolution aerosol mass spectroscopy (HR-AMS) with the specific aim of organic aerosol (OA) characterization and source apportionment. Eight intensive observation periods (IOPs) were carried out over 4 years (from 2011 to 2014) at two different sites (Bologna, BO, urban background, and San Pietro Capofiume, SPC, rural background), to characterize the spatial variability and seasonality of the OA sources, with a special focus on the cold season. On the multi-year basis of the study, the AMS observations show that OA accounts for averages of 45±8 % (ranging from 33 % to 58 %) and 46±7 % (ranging from 36 % to 50 %) of the total non-refractory submicron particle mass (PM1-NR) at the urban and rural sites, respectively. Primary organic aerosol (POA) comprises biomass burning (23±13 % of OA) and fossil fuel (12±7 %) contributions with a marked seasonality in concentration. As expected, the biomass burning contribution to POA is more significant at the rural site (urban / rural concentration ratio of 0.67), but it is also an important source of POA at the urban site during the cold season, with contributions ranging from 14 % to 38 % of the total OA mass. Secondary organic aerosol (SOA) contributes to OA mass to a much larger extent than POA at both sites throughout the year (69±16 % and 83±16 % at the urban and rural sites, respectively), with important implications for public health. Within the secondary fraction of OA, the measurements highlight the importance of biomass burning aging products during the cold season, even at the urban background site. This biomass burning SOA fraction represents 14 %–44 % of the total OA mass in the cold season, indicating that in this region a major contribution of combustion sources to PM mass is mediated by environmental conditions and atmospheric reactivity. Among the environmental factors controlling the formation of SOA in the Po Valley, the availability of liquid water in the aerosol was shown to play a key role in the cold season. We estimate that the organic fraction originating from aqueous reactions of biomass burning products (“bb-aqSOA”) represents 21 % (14 %–28 %) and 25 % (14 %–35 %) of the total OA mass and 44 % (32 %–56 %) and 61 % (21 %–100 %) of the SOA mass at the urban and rural sites, respectively.

scholarly journals Secondary organic aerosol formation from photooxidation of naphthalene and alkylnaphthalenes: implications for oxidation of intermediate volatility organic compounds (IVOCs)

2009 ◽  
Vol 9 (9) ◽  
pp. 3049-3060 ◽  
Author(s):  
A. W. H. Chan ◽  
K. E. Kautzman ◽  
P. S. Chhabra ◽  
J. D. Surratt ◽  
M. N. Chan ◽  
...  
Keyword(s):  
Gas Phase ◽  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Diesel Emissions ◽  
Aerosol Formation ◽  
Gas Phase Reactions ◽  
Large Source ◽  
Aerosol Mass ◽  
Polycyclic Aromatic ◽  
Primary Emissions

Abstract. Current atmospheric models do not include secondary organic aerosol (SOA) production from gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs). Recent studies have shown that primary emissions undergo oxidation in the gas phase, leading to SOA formation. This opens the possibility that low-volatility gas-phase precursors are a potentially large source of SOA. In this work, SOA formation from gas-phase photooxidation of naphthalene, 1-methylnaphthalene (1-MN), 2-methylnaphthalene (2-MN), and 1,2-dimethylnaphthalene (1,2-DMN) is studied in the Caltech dual 28-m3 chambers. Under high-NOx conditions and aerosol mass loadings between 10 and 40 μg m−3, the SOA yields (mass of SOA per mass of hydrocarbon reacted) ranged from 0.19 to 0.30 for naphthalene, 0.19 to 0.39 for 1-MN, 0.26 to 0.45 for 2-MN, and constant at 0.31 for 1,2-DMN. Under low-NOx conditions, the SOA yields were measured to be 0.73, 0.68, and 0.58, for naphthalene, 1-MN, and 2-MN, respectively. The SOA was observed to be semivolatile under high-NOx conditions and essentially nonvolatile under low-NOx conditions, owing to the higher fraction of ring-retaining products formed under low-NOx conditions. When applying these measured yields to estimate SOA formation from primary emissions of diesel engines and wood burning, PAHs are estimated to yield 3–5 times more SOA than light aromatic compounds over photooxidation timescales of less than 12 h. PAHs can also account for up to 54% of the total SOA from oxidation of diesel emissions, representing a potentially large source of urban SOA.

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