Search Results (10)

Biomass burning processes affect many semi-rural areas in the Mediterranean, but there is a lack of long-term datasets focusing on their classification, obtained by monitoring carbonaceous particle concentrations and optical properties variations. To address this issue, a campaign to measure equivalent black carbon (eBC) and particle number size distributions (0.3–10 μm) was carried out from August 2019 to November 2020 at a coastal semi-rural site in the Basilicata region of Southern Italy. Long-term datasets were useful for aerosol characterization, helping to clearly identify traffic as a constant eBC source. For a shorter period, PM_2.5 mass concentrations were also measured, allowing the estimation of elemental and organic carbon (EC and OC), and chemical and SEM (scanning electron microscope) analysis of aerosols collected on filters. This multi-instrumental approach enabled the discrimination among different biomass burning (BB) processes, and the analysis of three case studies related to domestic heating, regional smoke plume transport, and a local smoldering process. The AAE (Ångström absorption exponent) daily pattern was characterized as having a peak late in the morning and mean hourly values that were always higher than 1.3. Full article

A study of carbonaceous species, polycyclic aromatic hydrocarbons (PAHs), and nitro-PAHs associated with PM_2.5 was conducted to assess their carcinogenic potential and associated health risks in the two main cities of the State of Morelos: Cuernavaca and Cuautla. The annual median concentrations in Cuernavaca of organic carbon (OC) and elemental carbon (EC) were 6.2 µg m⁻³ and 0.6 µg m⁻³, respectively, whereas in Cuautla, OC concentrations averaged 4.8 µg m⁻³ and EC 0.6 µg m⁻³. OC/EC ratios, total carbonaceous aerosols (TCA), primary (POC) and secondary organic carbon (SOC), as well as elemental carbon reactive (ECR) were estimated, also showing prevalence of primary emissions such as biomass burning. The seventeen PAHs recommended by the EPA and twelve nitro-PAHs were measured using gas chromatography–mass spectrometry. The annual median sum of PAHs was 9.7 ng m⁻³ in Cuernavaca and 11.2 ng m⁻³ in Cuautla, where carcinogenic high-molecular-weight compounds were the most dominant; the annual median sums of nitro-PAHs were 287 pg m⁻³ and 432 pg m⁻³, respectively. Diagnostic ratios were applied to identify potential sources of PAH emissions, suggesting that fuel combustion is the major contributor in both sites, followed by coal biomass burning and agricultural activities. The annual carcinogenic potential as benzo(a)pyrene equivalent was 2.2 ng m⁻³ for both sites. The lifetime excess cancer risk from PAH inhalation was estimated to range from 1.8 × 10⁻⁴ to 2 × 10⁻⁴ in Cuernavaca and from 1.5 × 10⁻⁴ to 2.2 × 10⁻⁴ in Cuautla, similar to values observed in other urban regions globally. Full article

Intermediate-volatility organic compounds (IVOCs) serve as pivotal precursors to secondary organic aerosol (SOA). They are highly susceptible to substantial wall losses both in indoor environments and within smog chambers even with Teflon walls. Accurately characterizing the wall loss effects of IVOCs is thus essential for simulation studies aiming to replicate their atmospheric behaviors in smog chambers to ensure precise modeling of their physical and chemical processes, including SOA formation, yet a comprehensive understanding of the wall loss behavior of IVOCs remains elusive. In this study, we conducted a thorough characterization of wall losses for typical intermediate-volatility hydrocarbon compounds, including eight normal alkanes (n-alkanes) and eight polycyclic aromatic hydrocarbons (PAHs), using the smog chamber with a 30 m³ Teflon reactor. Changes in the concentrations of gaseous IVOCs with the chamber were observed under dark conditions, and the experimental data were fitted to the reversible gas–wall mass transfer theory to determine the key parameters such as the wall accommodation coefficient (α_w) and the equivalent organic aerosol concentration (C_w) for different species. Our results reveal that C_w values for these hydrocarbon IVOCs range from 0.02 to 5.41 mg/m³, which increase with volatility for the PAHs but are relative stable for alkanes with an average of 3.82 ± 0.92 mg/m³. α_w span from 1.24 × 10⁻⁷ to 1.01 × 10⁻⁶, with the values for n-alkanes initially showing an increase followed by a decrease as carbon numbers rise and volatility decreases. The average α_w for n-alkanes and PAHs are 3.34 × 10⁻⁷ and 6.53 × 10⁻⁷, respectively. Our study shows that IVOCs exhibit different loss rates onto clean chamber walls under dry and dark conditions, with increasing rate as the volatility decreases. This study demonstrates how parameters can be acquired to address wall losses when conducting smog chamber simulation on atmospheric processes of IVOCs. Full article

Norpinic acid is a major semi-volatile oxidation product of α-pinene and β-pinene, two of the most important biogenic atmospheric volatile organic compounds. In this study we characterized the physicochemical properties of norpinic acid aerosol using a variety of techniques, and we investigated its reaction with OH radicals. The Aerosol Mass Spectrometer (AMS) spectrum of norpinic acid was characterized by a pronounced peak at m/z 82 (C₅H₆O⁺), which can be used as its chemical signature. The measured density of norpinic acid particles was 1.3 g cm⁻³. Its saturation concentration at 298 K was estimated to be equal to 8.9 μg m⁻³ using thermodenuder measurements and 12.8 μg m⁻³ using isothermal dilution. Its vaporization enthalpy was equal to 71 kJ mol⁻¹. After reaction with OH radicals for an equivalent atmospheric period of 0.6–5 days under UV radiation and low RH, there were no noticeable changes in the AMS spectrum of the particles, while the wall-loss corrected mass concentration slightly decreased. This suggests that the atmospheric aging products of norpinic acid particles are quite similar to the parent molecule when measured by the AMS, and the aging reactions lead to a small change in particle mass concentration. Full article

This article presents the results of the long-term studies at two stations located in the city of Irkutsk and the Listvyanka settlement of the southern Baikal region (East Siberia) concerning the concentration of polycyclic aromatic hydrocarbons (PAHs) in atmospheric aerosol. The studies revealed the seasonal and interannual dynamics in the distribution of PAHs in aerosols from urban (source) and rural (receptor) areas. We carried out a comprehensive analysis of weather conditions such as wind direction, relative humidity, air temperature, and atmospheric pressure. The analysis determined high correlations between air temperature, atmospheric pressure, temperature inversions, and PAHs at the monitoring stations. The average annual concentrations of PAHs in the abnormally warm 2020 were three times lower than the average values obtained in the cold 2016. The toxic equivalent concentrations (BaPeq) increased from summer to winter with an increase in the contribution from benzo(a)pyrene, one of the most toxic and hazardous compounds of this class of organic substances. Four-, five- and six-ring PAHs mainly predominated in aerosol; the proportion of two- and three-ring PAHs increased from the warm season to the cold season. Diagnostic ratios of PAHs identified the main sources of air pollution by this class of compounds: combustion of coal, liquid fuel and firewood, vehicle emissions, and wildfires. The percentage of the transport of anthropogenic aerosol containing PAHs from industrial sources of the Southern Baikal region towards Lake Baikal was 65 to 71%. Full article

Port cities are affected by a wide array of emissions, including those from the shipping, road transport, and residential sectors; therefore, the characterization and apportionment of such sources in a high temporal resolution is crucial. This study presents measurements of fine aerosol chemical composition in Piraeus, one of the largest European ports, during two monthly periods (winter vs. summer) in 2018–2019, using online instrumentation (Aerosol Chemical Speciation Monitor—ACSM, 7-λ aethalometer). PMF source apportionment was performed on the ACSM mass spectra to quantify organic aerosol (OA) components, while equivalent black carbon (BC) was decomposed to its fossil fuel combustion and biomass burning (BB) fractions. The combined traffic, shipping and, especially, residential emissions led to considerably elevated submicron aerosol levels (22.8 μg m⁻³) in winter, which frequently became episodic late at night under stagnant conditions. Carbonaceous compounds comprised the major portion of this submicron aerosol in winter, with mean OA and BC contributions of 61% (13.9 μg m⁻³) and 16% (3.7 μg m⁻³), respectively. The contribution of BB to BC concentrations was considerable and spatially uniform. OA related to BB emissions (fresh and processed) and hydrocarbon-like OA (from vehicular traffic and port-related fossil fuel emissions including shipping) accounted for 37% and 30% of OA, respectively. In summer, the average PM₁ concentration was significantly lower (14.8 μg m⁻³) and less variable, especially for the components associated with secondary aerosols (such as OA and sulfate). The effect of the port sector was evident in summer and maintained BC concentrations at high levels (2.8 μg m⁻³), despite the absence of BB and improved atmospheric dispersion. Oxygenated components yielded over 70% of OA in summer, with the more oxidized secondary component of regional origin being dominant (41%) despite the intensity of local sources, in the Piraeus environment. In general, with respect to local sources that can be the target of mitigation policies, this work highlights the importance of port-related activities but also reveals the extensive wintertime impact of residential wood burning. While a separation of the BB source is feasible, more research is needed on how to disentangle the short-term effects of different fossil-fuel combustion sources. Full article

In the current study, the photooxidation reaction of toluene (C₇H₈) was investigated in a Potential Aerosol Mass Oxidation Flow Reactor (PAM OFR). The hydroxyl radical (OH) exposure of toluene in the PAM OFR ranged from 0.4 to 1.4 × 10¹² molec cm⁻³ s, which is equivalent to 3 to 12 days of atmospheric oxidation. A proton transfer reaction-mass spectrometer (PTR-MS) and a scanning mobility particle sizer (SMPS) were used to study the gas-phase products formed and particle number changes of the oxidation reaction in PAM OFR. The secondary organic aerosol (SOA) formed in the PAM OFR was also collected for off-line chemical analysis. Key gas-phase reaction products of toluene, including glyoxal, methyl glyoxal, unsaturated carbonyl compounds, and benzaldehyde, were identified by the PTR-MS. Second generation products, including acetic acid, formaldehyde, formic acid, and acetaldehyde, were also detected. By comparing the mass spectrums obtained under different OH exposures and relative humidity (RH), changes in the two parameters have minimal effects on the composition of gas-phase products formed, expect for the spectrum obtained at OH exposure of 0.4 × 10¹² cm⁻³ s and RH = 17%, which is slightly different from other spectrums. SMPS results showed that particle mass concentration increases with increasing OH exposure, while particle number concentration first increases and then decreases with increasing OH exposure. This result probably suggests the formation of oligomers at high OH exposure conditions. Off-line chemical analysis of the SOA sample was dominated by C4 diacids, including malic acid, citramalic acid, and tartaric acid. The well-known toluene SOA marker 2,3-Dihydroxy-4-oxopentanoic acid, as well as 2,3-dihydroxyglutaric acid, which has not been identified in previous toluene photooxidation experiments, were also detected in the SOA sample. Our results showed good agreements with the results of previous smog chamber studies of toluene photooxidation reaction, and they suggested that using PAM OFR for studies of oxidation reaction of different VOCs can be atmospherically relevant. Full article

Concentrations of aerosol particles in Poland and their sources are rarely discussed in peer-reviewed journal articles despite serious air quality issues. A source apportionment of carbonaceous aerosol particles was performed during winter at a rural background environment field site in north-eastern Poland. Data were used of light absorption at seven wavelengths and levoglucosan concentrations along existing monitoring of PM_2.5, organic carbon and elemental carbon (OC/EC) at the Diabła Góra EMEP monitoring site between January 17 and March 19 during the EMEP intensive winter campaign of 2018. Average PM_2.5, OC, EC, equivalent black carbon (eBC) and levoglucosan concentrations and standard deviations amounted to 18.5 ± 9.3, 4.5 ± 2.5, 0.57 ± 0.28, 1.04 ± 0.62 and 0.134 ± 0.084 µg m⁻³ respectively. Various tools for source apportionment were used to obtain a source contribution to carbonaceous matter (CM) with three components. The wood combustion source component contributed 1.63 µg m⁻³ (21%), domestic coal combustion 3.3 µg m⁻³ (41%) and road transport exhaust 2.9 µg m⁻³ (38%). Similar levels and temporal variability were found for the nearby Lithuanian site of Preila, corroborating the Polish results. Full article

New emerging issues appears regarding the possible aerosolization of micro-organisms from biofilters to the ambient air. Traditional bioaerosol sampling and cultural methods used in literature offer relative efficiencies. In this study, a new method revolving around a particle counter capable of detecting total and viable particles in real time was used. This counter (BioTrak 9510-BD) uses laser-induced fluorescence (LIF) technology to determine the biological nature of the particle. The concentration of viable particles was measured on two semi-industrial pilot scale biofilters in order to estimate the Removal Efficiency in viable particles (RE_vp) in stable conditions and to examine the influence of pollutant feeding and relative humidification of the gaseous effluent on the RE_vp. The RE_vp of biofilters reached near 80% and highlighted both the stability of that removal and the statistical equivalence between two identical biofilters. Pollutant deprivation periods of 12 h, 48 h and 30 days were shown to have no influence on the biofilters’ removal capacity, demonstrating the robustness and adaptation capacities of the flora. In contrast, a 90-day famine period turned the biofilters into emitters of viable particles. Finally, the humidification of the effluent was shown to negatively influence the removal capacity for viable particles, as drying off the air was shown to increase the RE_vp from 60 to 85%. Full article

The objective of this work was to assess the yearly contribution of fossil fuel combustion (BC_ff) and wood burning (BC_wb) to equivalent black carbon (eBC) concentrations, in Athens, Greece. Measurements were conducted at a suburban site from March 2013 to February 2014 and included absorption coefficients at seven wavelengths and PM_2.5 chemical composition data for key biomass burning markers, i.e., levoglucosan, potassium (K) and elemental and organic carbon (EC, OC). A well-documented methodology of corrections for aethalometer attenuation coefficients was applied with a resulting annual dataset of derived absorption coefficients for the suburban Athens’ atmospheric aerosol. The Aethalometer model was applied for the source apportionment of eBC. An optimum Ångström exponent for fossil fuel (α_ff) was found, based on the combined use of the model with levoglucosan data. The measured eBC concentrations were equal to 2.4 ± 1.0 μg m⁻³ and 1.6 ± 0.6 μg m⁻³, during the cold and the warm period respectively. The contribution from wood burning was significantly higher during the cold period (21 ± 11%, versus 6 ± 7% in the warm period). BC_ff displayed a clear diurnal pattern with a morning peak between 8 and 10 a.m. (during morning rush hour) and a second peak during the evening and night hours, due to the shallowing of the mixing layer. Regression analysis between BC_wb concentrations and biomass burning markers (levoglucosan, K and OC/EC ratio) supported the validity of the results. Full article