Kalliopi
Florou
a,
John K.
Kodros
a,
Marco
Paglione
ab,
Spiro
Jorga
c,
Stefania
Squizzato
a,
Mauro
Masiol
ad,
Petro
Uruci
ae,
Athanasios
Nenes
af and
Spyros N.
Pandis
*ae
aInstitute of Chemical Engineering Sciences, ICE-HT, Patras, 26504, Greece
bInstitute of Atmospheric Sciences and Climate, Italian National Research Council, Bologna 40129, Italy
cDepartment of Chemical Engineering, Carnegie Mellon University, Pittsburgh, 15213, USA
dDepartment of Environmental Sciences, Informatics and Statistics, Università Ca' Foscari Venezia, Venice, Italy
eDepartment of Chemical Engineering, University of Patras, Patras 26504, Greece. E-mail: spyros@chemeng.upatras.gr
fSchool of Architecture, Civil and Environmental Engineering, Swiss Federal Institute of Technology Lausanne, Lausanne 1015, Switzerland
First published on 28th July 2023
Pellet combustion in residential heating stoves has increased globally during the last decade. Despite their high combustion efficiency, the widespread use of pellet stoves is expected to adversely impact air quality. The atmospheric aging of pellet emissions has received even less attention, focusing mainly on daytime conditions, while the degree to which pellet emissions undergo night-time aging as well as the role of relative humidity remain poorly understood. In this study, environmental simulation chamber experiments were performed to characterize the fresh and aged organic aerosol (OA) emitted by a pellet stove. The fresh pellet stove PM1 (particulate matter with an aerodynamic diameter less than 1 μm) emissions consisted mainly of OA (93 ± 4%, mean ± standard deviation) and black carbon (5 ± 3%). The primary OA (POA) oxygen-to-carbon ratio (O:C) was 0.58 ± 0.04, higher than that of fresh logwood emissions. The fresh OA at a concentration of 70 μg m−3 (after dilution and equilibration in the chamber) consisted of semi-volatile (68%), low and extremely low volatility (16%) and intermediate-volatility (16%) compounds. The oxidation of pellet emissions under dark conditions was investigated by injecting nitrogen dioxide (NO2) and ozone (O3) into the chamber, at different (10–80%) relative humidity (RH) levels. In all dark aging experiments secondary organic aerosol (SOA) formation was observed, increasing the OA levels after a few hours of exposure to NO3 radicals. The change in the aerosol composition and the extent of oxidation depended on RH. For low RH, the SOA mass formed was up to 30% of the initial OA, accompanied by a moderate change in both O:C levels (7–8% increase) and the OA spectrum. Aging under higher RH conditions (60–80%) led to a more oxygenated aerosol (increase in O:C of 11–18%), but only a minor (1–10%) increase in OA mass. The increase in O:C at high RH indicates the importance of heterogeneous aqueous reactions in this system, that oxidize the original OA with a relatively small net change in the OA mass. These results show that the OA in pellet emissions can chemically evolve under low photochemical activity (e.g. the wintertime period) with important enhancement in SOA mass under certain conditions.
Environmental significancePellet combustion in residential heating stoves has increased globally during the last decade. However, this potentially important air pollution source has received relatively little attention compared to other sources of biomass burning. In this work we show that the corresponding emissions evolve chemically as they react during the night and day and that the corresponding production of secondary organic aerosol is quite different from that of logwood combustion. These results indicate that the emissions from pellet combustion need to be separated from the rest of the residential heating emissions and should be treated differently in chemical transport models. The characterization results (emission rates, composition, volatility distribution, etc.) can be used for the simulation of these emissions in the same models. |
During the wintertime wood burning is one of the most important sources of organic aerosol (OA). Emissions consist of both primary organic aerosol (POA) and organic vapors that can be oxidized producing secondary organic aerosol (SOA).10–13 Pellet stoves are typically considered low-emitting burners,14–16 since they emit less particulate matter (PM)17,18 and carbon monoxide (CO) than modern wood stoves.4,19 A growing influence of their emissions on air pollution is expected. In 2018, global wood pellet consumption increased by 130% compared to its 2013 levels, reaching 53 million tons.2 Half of this consumption took place in Europe (27 million tons; a 60% increase in 5 years), where pellet consumption, for heating purposes only, increased by 220% during the 2013–2018 period, accounting for 15.8 million tons in 2018.2 In 2019, European pellet consumption increased by 7%, an increase of 1.8 million tons in just one year.20
The fresh emissions of pellet stoves consist mainly of OA and black carbon (BC),7 carbon dioxide and monoxide, nitrogen oxides, and a wide range of volatile organic compounds (VOCs).19,21 Bertrand et al.5 reported that the dominant (up to 90%) PM component of fresh pellet emissions was BC (concentrations higher than 100 μg m−3). The oxygen-to-carbon ratio (O:C) of OA was in the range of 0.2–0.6,5,7 with fresh emitted particles having a mass distribution with a mode at around 0.1 μm.4,22 The pellet OA density was found to range between 1020 kg m−3 and 1350 kg m−3.23,24 Differences in the emissions of different pellet types,8,25,26 the importance of different pellet burner operations7,27 and the significance of having ideal and non-ideal burning conditions28 have been underlined in previous studies.
The atmospheric aging of pellet emissions has received relatively little attention. Few previous studies have investigated SOA formation using chambers or flow reactors focusing on the oxidation of pellet emissions in the presence of sunlight (i.e., via the OH radical). Bertrand et al.5 found that the OA mass increased by a factor of 1.5 to 1.9, after simulating atmospheric aging using ultraviolet light (UV), while Corbin et al.6 reported only minor amounts of SOA production relative to their primary OA emission from modern pellet stoves. Heringa et al.7 examined the aging of the emissions during different burning phases of a pellet burner (stable burning and starting) concluding that the O:C of OA increased in all cases, but SOA formation was quite variable ranging from low to a factor of 3.3 of the fresh OA, depending on the burning phase. Reyes et al.29 compared firewood and pellet emissions and concluded that firewood combustion emissions are more rapidly oxidized.
Recently, there has been growing interest in exploring the extent of atmospheric processing of biomass burning emissions during the night-time.30,31 Hartikainen et al.32 reported substantial SOA production in laboratory experiments aging logwood combustion emissions under dark conditions. Kodros et al.33 showed that fresh emissions from wood burning exposed to NO3 radicals rapidly formed oxygenated OA (OOA) and organic nitrate compounds. The extent of oxidation was sensitive to relative humidity (RH) and consistently showed greater enhancement in the O:C ratio under high RH conditions, suggesting a sensitivity of the aging process to water vapor and/or aerosol liquid water content.34–36 Jorga et al.,37 using a dual chamber system and ambient air during the wintertime, observed rapid SOA formation corresponding to 20–70% of the pre-existing OA, with secondary organic nitrate accounting for up to 85% of total aerosol nitrate. The SOA produced in both studies was chemically similar to ambient observations of oxidized OA factors.38–40
Despite these previous studies, aging of pellet emissions in the absence of sunlight has received little or no attention. In this study, we performed environmental smog chamber experiments to characterize fresh pellet stove emissions using high commercially available fuel class quality fuel and a modern pellet unit. Pellet combustion was representative of residential heating in an urban environment. The oxidation of fresh pellet emissions under dark conditions was investigated by injecting different concentrations of both nitrogen dioxide (NO2) and ozone (O3), at low and high relative humidity levels. We compared these dark-aging experiments to 3 reference experiments: two experiments without any external initiation of oxidation and one experiment under exposure to UV lights. The results were additionally compared to those of logwood burning in an effort to distinguish the two biomass burning sources.
Pellets of the highest commercially available fuel class quality (defined by ISO 17225-2: ENplus A1; RH < 10%) were burned in a pellet stove (Atena 80, with a heat output of 3–6.7 kW) operated in its automatic mode. Both stem conifer wood and chemically untreated by-products were used as raw materials for pellet production. The fuel consumption in our experiments was 1.1 kg h−1, which is approximately in the middle of the range for this stove. The wood pellets had a diameter of 6–8 mm and a length of 5–20 mm. Both the fuel and pellet stove are commercially available in the European market and represent characteristic fuel and heating devices used in Greece.
The pellet combustion facility is located in the basement of the building, directly underneath the atmospheric simulation chamber (Fig. 1). In all experiments, we injected the pellet emissions into the chamber approximately 10–20 minutes after ignition under flaming conditions.
Fig. 1 Schematic of the FORTH-ASC combustion chamber, pellet burning facilities and instrumentation. |
The pellet combustion emissions were directed into the environmental chamber, passing through a dilution system. The tubing used in the injection system was stainless steel (3/8 prior to the diluter and 1/2 after the diluter) and all lines were insulated. The corresponding selection was made to minimize losses of particles, but some adsorption of the gas-phase organics to the tubing can be expected. The flow was in the laminar regime. Emissions were diluted by approximately a factor of 10 with clean air. The chamber was pre-filled and the dilution in the chamber was close to 1:30. The target was an OA mass concentration in the range of 40–200 μg m−3, which corresponds to observed atmospheric OA levels during periods of intense residential biomass burning.
The fresh emissions were allowed to equilibrate in the dark chamber for approximately 2 hours to allow sufficient time for mixing and characterization. After this period, NO2 and O3 were injected in the dark. We define the injection of O3 as time zero for all dark-aging experiments. In the three reference experiments time zero is the time when the emissions were exposed to UV (Exp. 7) or when the pellet emissions were injected into the chamber without any extra addition of NO2 and O3 (Exp. 8 and 9; Table 1). Isotopically labelled butanol d-9 was added to the chamber to estimate OH levels.41 Prior to each experiment the chamber was cleaned overnight by flushing it with clean air.
Exp. | Pellet burning emissions | Experimental conditions | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
OA [μg m−3] | BC [μg m−3] | Nitrate [μg m−3] | Total PM1 [μg m−3] | f 44/f60 | O:C | H:C | VOCs/NOx | MCE | Lights | RH [%] | T [°C] | O3 [ppb] | NO2 [ppb] | |
a In experiments 7–9, no additional NO2 or O3 was injected. | ||||||||||||||
1 | 42 | 0.6 | 0.4 | 43.2 | 0.66 | 0.53 | 1.74 | 2.80 | 0.97 | Dark | 8 | 21 | 55 | 50 |
2 | 204 | 4.7 | 2 | 211.4 | 0.51 | 0.56 | 1.73 | 1.72 | 0.96 | Dark | 9 | 22 | 100 | 100 |
3 | 93 | 6.9 | 0.9 | 101.5 | 0.66 | 0.55 | 1.75 | 0.74 | 0.97 | Dark | 9 | 22 | 100 | 90 |
4 | 62 | 5.5 | 1.5 | 69.4 | 0.72 | 0.58 | 1.77 | 0.45 | 0.92 | Dark | 80 | 20 | 90 | 90 |
5 | 78 | 3 | 2.2 | 83.4 | 0.58 | 0.57 | 1.77 | 3.15 | 0.92 | Dark | 80 | 20 | 45 | 40 |
6 | 58 | 4.2 | 5 | 70.2 | 0.76 | 0.65 | 1.76 | 0.98 | 0.92 | Dark | 60 | 18 | 100 | 110 |
7 | 67 | 1.5 | 0.4 | 69.2 | 1.11 | 0.54 | 1.73 | 54.12 | 0.96 | UV | 10 | 22 | (10)a | (0.3)a |
8 | 84 | 2.6 | 1.8 | 90.6 | 1.57 | 0.57 | 1.69 | 6.50 | 0.93 | Dark | 15 | 20 | (27)a | (4.5)a |
9 | 74 | 4.2 | 0.9 | 81.9 | 0.62 | 0.64 | 1.80 | 5.77 | 0.96 | Dark | 9 | 22 | (17)a | (4.7)a |
We tried to quantify the extent of losses of semivolatile organic vapors in the chamber by allowing the emissions to remain undisturbed for up to 12 h. No changes in the particle composition in the chamber were observed using the AMS. Also the small changes in the OA mass concentration were consistent with the measured particle wall losses in the FORTH chamber. These observations indicate that the losses of semi-volatile and lower-volatility organics to the walls during our experiments were relatively low.
Parallel to the AMS, a scanning mobility particle sizer (SMPS; classifier model 3080, DMA model 3081, CPC model 3787, TSI Incorporated) was used, with a sheath flow rate set at 3 L min−1 and an aerosol sample flow rate of 0.6 L min−1, measuring the particulate number size distribution for mobility diameters ranging between 14 and 710 nm every 3 min. A multiple-angle absorption photometer (MAAP, Thermo Scientific Inc.)45 was deployed to determine the BC levels. Due to its high flow (16.7 L min−1), the MAAP was sampling from the chamber for 10 min every half hour, with a time resolution of 1 min. A mass absorption cross section of BC of 6.6 m2 g−1 at a wavelength of 637 nm was assumed for the estimation of the BC concentration.
The OA volatility was measured using a thermodenuder (TD).46,47 The measurements were analyzed using the Karnezi et al.48 algorithm to estimate the volatility distribution of OA.49 The TD consists of a heated tube where more volatile compounds evaporate followed by a cooling section with activated carbon to avoid vapor condensation. The TD was combined with the SMPS and the AMS to measure the aerosol mass fraction remaining (MFR) in a selected range of temperatures. The mass transfer in TDs depends on the initial OA concentration, the residence time in the heating tube, the vaporization enthalpy of the OA, and any mass transfer resistances.
The concentration of VOCs was measured using a proton-transfer-reaction mass spectrometer (PTR-QMS 500, Ionicon Analytik). The reaction reagent for the PTR-QMS was H3O+. The drift tube was operated at 600 V at a constant pressure of 2.2–2.3 mbar and the sampling flow rate was 0.5 L min−1. The calibration followed the procedure described by Kaltsonoudis et al.50 using VOC standards obtained from Ionicon.
A suite of Teledyne gas monitors was used to monitor the concentration of nitrogen oxides and ammonia (T201), ozone (O3; 400E), carbon monoxide (CO; 300E), and carbon dioxide (CO2; T360). Gas monitors were routinely calibrated.
Sampling on 47 mm PTFE filters (Pall Corporation, 1 cm diameter of the collection surface) was performed at a flow rate of 8 L min−1 for 20 min for primary and aged PM1 pellet emissions in order to perform offline Fourier transform infrared spectroscopy (FTIR). Details about the FTIR analysis can be found in Yazdani et al.51
The size-dependent particle wall loss rate constants were measured after each experiment using ammonium sulfate seeds.53,54 Particles were produced using an atomizer and after passing through a dryer they were introduced to the chamber directly. The corresponding wall loss rate constants were nearly constant across particle diameters in the range of 60–700 nm. We corrected AMS mass concentrations using the average wall loss rate constant (0.06 ± 0.02 h−1) at the mean vacuum aerodynamic diameter of the OA mass distribution (170 nm).
To explore the range of solutions of the TD model, we discretized the domain of the parameters and simulated all combinations of volatilities, the vaporization enthalpy (ΔHvap), and the accommodation coefficient (αm). We used 7 bins for the volatility ranging from 10−3 to 103 μg m−3 and varied the mass fraction from 0 to 1 with a step of 0.1, leading to around 8000 different combinations. The values used for ΔHvap ranged from 20 to 200 kJ mol−1 with a step of 20 kJ mol−1, and for αm, the discrete values are 0.001, 0.01, 0.1, and 1. Around 320000 simulations were performed for all combinations of all properties, from which we identified those that led to errors less than 1%. Then we calculated the best estimate following the approach described by Karnezi et al.48 The one-dimensional volatility basis set (1 D-VBS) framework has been designed to help describe the volatility distribution of OA. The 1D-VBS utilizes logarithmically spaced bins based on an effective saturation concentration at 298 K.55
The theta angle (θ) was used to quantify the variation in the SOA mass spectra measured using the AMS.56 The theta angle is the inner product of mass spectra treated like n-dimensional vectors (where n is the number of mass-to-charge ratio, m/z, values). A theta angle of 10° or less indicates high similarity, while higher values (more than 25°) suggest significant differences between the two spectra.
Particulate organic nitrate (ON) was estimated based on the NO2+/NO+ ratio.57–59 In this work, the measured NO2+/NO+ ratio for pure ammonium nitrate (NH4NO3) was equal to 0.82, while the minimum observed NO2+/NO+ratio during all experiments was 0.04.
OH radical concentrations were estimated from the change in the concentration of the PTR-MS m/z 66 which corresponds to the isotopically labeled butanol-d9 (98%, Cambridge Isotope Laboratories). The corresponding reaction rate constant used was 3.4 × 10−12 cm3 per molecule per s.41 One photochemical day was defined as continued 24 h OH exposure at a concentration of 1.5 × 106 molecules per cm3.60,61
The acidity of the wood pellet burning aerosol was estimated using a procedure similar to that by Kodros et al.,62 using the aerosol thermodynamics model ISORROPIA-lite.63 ISORROPIA-lite is based on the ISORROPIA-II64 model but extended to account for the effects of water uptake from the organic aerosol that may exist, parameterized according to κ-Köhler theory.65 Inputs to the model include the relative humidity, temperature, the OA concentration, hygroscopicity parameter κ and density and the total (gas- and particle-phase) concentrations of ammonia/ammonium, sulfuric acid, sodium, calcium, potassium, magnesium, chloride/hydrochloric acid, and nitrate/nitric acid. A κ value equal to 0.15 was used.66 We assumed that the total nitric acid and hydrochloric acid concentrations were equal to the AMS-measured inorganic nitrate and chloride concentrations, respectively. This is a good assumption, given that the biomass burning aerosol pH is expected to be high enough so that most of the nitrate and chloride are in the aerosol phase.62,67 The potassium concentration was scaled as 15% of the PM nitrate.68 The concentrations of non-volatile cations such as sodium, calcium, and magnesium were assumed to be zero as their contribution to the sub-micrometer mode is considered to be negligible.69 For the submicron particles considered here and room temperature, the above methodology for pH estimation is expected to be reliable, albeit with the same limitations as when applied to ambient data. Pye et al.69 provide a thorough summary of the literature on the applicability of equilibrium models and associated errors for pH estimation.
The time dependent AMS CE was determined to be on average 0.8 ± 0.2 (one standard deviation, SD) and the average OA density calculated based on the Kostenidou et al.52 algorithm was 1.21 ± 0.07 (mean ± SD) g cm−3. For comparison, the estimated OA density based on the measured O:C and hydrogen-to-carbon (H:C) elemental ratios as suggested by Kuwata et al.70 was on average 1.26 ± 0.02 (mean ± SD) g cm−3. Based on the results of the two methods, an average density of 1.25 g cm−3 was selected to characterize the fresh pellet emissions.
In all experiments, the fresh pellet stove emissions were dominated by OA, which represented 93 ± 4% of the measured PM1. Nitrate and OA had similar size distributions and mean diameters, indicating an internally mixed aerosol. With the exception of nitrate, the concentrations of the rest of the aerosol components measured using the AMS (sum of sulfate, ammonium and chloride) accounted for less than 3% of the aerosol mass (Table 1). Due to their low concentrations their corresponding AMS size distributions were quite noisy. The measured BC varied between 0.6 and 7 μg m−3, accounting for 1–8% of the measured PM1. This is in contrast to the study by Bertrand et al.,5 where BC was the dominant component (90%) of the fresh pellet emission. This difference is likely related to the operating conditions of the stove used in that study, as well as the choice of fuel which in the present study had high energy density (>4.6 kW h kg−1) with less than 10% moisture and a low percentage of ash (<0.7). The average organic aerosol to black carbon ratio (OA/BC) was 34 ± 24 which is higher than that reported by Heringa et al.7 (2.5 ± 0.9). A high OA/BC ratio usually indicates good combustion conditions. Our results are consistent with the measurements of McClure et al.71 who tested a number of biomass fuels and reported OA/BC ratios varying between 0.3 and 10.5 For example, for pine the OA/BC ranged between 7 and 143, while in our case the OA/BC ranged between 14 and 83.
Total nitrate (inorganic plus organic) accounted on average for 0.5–4% of the PM1 ranging between 0.4 and 2.5 μg m−3, while sulfate and chloride contributed equally 0.8%. Ammonium was less than 0.1% of the PM1 in all experiments. The organic nitrate fraction of total nitrate (see Section 2.2) was on average 31 ± 18% (Fig. S1†). The O:C of the fresh OA varied between 0.53 and 0.65 (Table 1) and is consistent with that in previous studies.5,7 The organic-mass-to-organic-carbon ratio (OM/OC) was on average 1.92 ± 0.04 (mean ± SD).
The AMS mass spectrum of the fresh biomass burning OA (bbOA) exhibited moderate variability across the various experiments with the theta angle between pairs of experiments varying between 3 and 18° (Table S1†). The average high resolution (HR) fresh OA spectrum from all experiments is shown in Fig. 2. The spectrum is characterized by prominent peaks at m/z 29 (CHO+ and C2H5+), 39 (C3H3+), 43 (C2H3O+), 44 (CO2+ and C2H4O+), 55 (C3H3O+ and C4H7+), 57 (C3H5O+), 60 (C2H4O2+), 73 (C3H5O2+), 91 (C7H7+), 115 (C9H7+), 137 (C8H9O2+) and 151 (C8H7O3+). These fragments contributed 36 ± 2% of the total organic mass. The OA spectrum resembled the HR spectrum of primary pellet stove emissions reported in previous studies5 but with a stronger signal at m/z 29, 43, 44, 60, 73 and 137. The HR spectrum of OA mainly consisted of CxHyO+ (39%), followed by CxHy+ (35%) and CxHyOz+ (22%) with the rest of the families contributing 4% (Fig. 2a). The variability of the OA mass spectra of all fresh pellet emissions is shown in Fig. S1.†
While various VOCs are emitted by biomass burning, the PTR-MS measures only a limited VOC range (the ones that can be protonated). The measured VOC to NOx ratios for the different experiments are shown in Table 1. The main gas-phase compounds and/or fragments of compounds measured using the PTR-MS in the environmental chamber after the injection period were phenolic compounds, furans and monoterpenes (Fig. 2b).
The major phenolic compounds detected were phenol (m/z 95), cresol (m/z 109), creosol (m/z 139), and 4-vinylguaiacol (m/z 151) which are commonly formed from thermal decomposition of lignin and are a significant component of biomass burning emissions.32,72 The m/z 151 could also be related to pinonaldehyde, but 4-vinylguaiacol was detected in previous studies of fire emissions.72
Furans are emitted into the atmosphere during biomass burning as products of the pyrolysis of cellulose.73 Furanoic emissions were dominated by furfural (m/z 97), which is considered a biomass burning marker74 and was also detected in pellet emissions.14 Monoterpenes (m/z 81 and m/z 137) detected with the PTR-MS were significant in all experiments. Other gas-phase compounds that were measured in the pellet emissions were: m/z 43 (alkyl fragments, propylene, acetic acid, acetone, and peroxyacetyl nitrate (PAN)), m/z 45 (acetaldehyde), m/z 57 (acrolein), m/z 73 (methyl ethyl ketone (MEK)), m/z 85 (ethyl vinyl ketone (EVK)), and m/z 87 (2-methyl-3-buten-2-ol (MBO)). Some of these VOCs (m/z 43, 45, 99, and 139) have been detected in pellet stove exhaust previously.14,75 Aromatic hydrocarbons such as benzene (m/z 79), toluene (m/z 93), xylenes/ethylbenzene (m/z 107), C10 aromatics (m/z 135), and C11 aromatics (m/z 149) were present in the emissions but were less than 1–2 ppb.
The modified combustion efficiency (MCE) is defined as the ratio of carbon emitted as carbon dioxide (CO2) to the total amount of carbon emitted as CO2 and CO and is a key metric of combustion.76 In general, a MCE value equal to one corresponds to complete combustion, while values between 0.9 and 1 indicate flaming conditions, and values of 0.85 and less indicate smoldering conditions.77 The arithmetic average MCE from the 9 experiments was 0.94 ± 0.02 (mean ± SD), with the lowest MCE values calculated for experiments 4–6 (Table 1).
In all experiments, the particle number distribution of the fresh emissions was unimodal. The calculated mean particle mobility diameter from the SMPS measurements during the emission period varied between 85 and 125 nm, with an average diameter of 106 nm and a modal width, σ, equal to 1.54. The variability in particle diameter is due to both small changes in the combustion conditions and coagulation of the fresh emissions. In previous studies, the number size distribution of pellet emissions was dominated by submicron particles with a maximum size in the range of around 150 nm.78
In two experiments the emissions were allowed to reside undisturbed in the dark chamber for 12 h. After particle wall-loss corrections were applied, no detectable changes in the mass, AMS spectrum and O:C ratio were observed, suggesting that low and semi-volatile vapor wall losses were not a dominant factor in our experiments.
The TD operated in a temperature range between 25 °C and 185 °C using several temperature steps. The centerline residence time of the aerosol in the TD was 16 s at 298 K. The OA mass fraction remaining (MFR) was calculated as the ratio of the organic mass concentration of a sample passing through the TD at time ti over the average mass concentration of the bypass sample at times ti−1 and ti+1.
The thermodenuded OA was corrected for the AMS CE (average CETD = 0.9 ± 0.04) and for particle losses in the TD. The particle losses were measured as a function of temperature and particle size in an additional experiment using sodium chloride particles. The average loss fraction in the 0.1–1 μm size range for each temperature was used for the correction of the AMS results.47
The initial mass concentration in the TD was 70 μg m−3 and the mean volume diameter was 170 nm. The OA density (ρOA) was equal to 1.25 g cm−3. Approximately 80% of the OA evaporated at 90 °C (Fig. 3a). At 180 °C, 9% of the initial OA remained in the particulate phase.
Fig. 3 (a) Thermogram of the OA TD measurements of Exp. 8. Red dots represent the loss-corrected measurements. The black line represents the best estimate, and the gray area is the uncertainty range estimated using the model by Karnezi et al.48 (b) Estimated volatility distributions of the OA. The error bars represent the uncertainty calculated using the model. The ELVOCs in the 1 D-VBS framework are in the gray area, the LVOCs are in the red, the SVOCs are in the green, and the IVOCs are in the blue-shaded area. |
Applying the approach by Karnezi et al.,48 we determined the volatility distribution for the emitted OA by pellets. The model reproduced the measurements well (Fig. 3b). Our model results suggest that the pellet OA at 70 μg m−3 consisted of 11% extremely low-volatility compounds (ELVOCs), 5% low-volatility compounds (LVOCs), 68% semi-volatile compounds (SVOCs), and 16% intermediate-volatility compounds (IVOCs) (Fig. 3b). The estimated effective enthalpy of vaporization was equal to 77 ± 20 (mean ± SD) kJ mol−1, and the effective accommodation coefficient was 0.2 with an uncertainty range covering more than an order of magnitude.
After leaving the pellet emissions for approximately 2 h in the dark, reactions were initiated with an injection of 55 ppb of O3 (t = 0) (Fig. 4a). Then the system was monitored for another 4 h for chemical processing and characterization of the aged aerosol and vapors. Following the O3 injection, formation of SOA and particulate organic nitrate was observed (Fig. 4b). After 4 h the OA increased by 11 μg m−3 (an increase of 21%), while the organic nitrate increased by 0.7 μg m−3 (Fig. 4b).
The degree of chemical processing of biomass burning OA (bbOA) was quantified using both the change in the O:C and the theta angle of its AMS spectrum compared with that of the fresh OA. Before time zero and the initiation of dark oxidation, both metrics were stable (change less than 3%), suggesting that the bbOA was well mixed and stable in the chamber (Fig. 4c). After 4 h of dark aging following the O3 injection, the O:C ratio increased by 0.05 (10% increase), while a small change in the OA AMS spectrum was observed (θ = 8°) (Fig. 4c), indicating evolution of the bbOA spectrum to some extent, but still maintaining similarity to the fresh bbOA.
During the same period the levels of several VOCs decreased. Furfural (m/z 97) displayed higher reduction (45%) (Fig. 4d), while phenolic compounds such as phenol (m/z 95) and cresol (m/z 109) both decreased by 13%. Monoterpenes (m/z 81 and m/z 137) were reduced by around 10% and xylenes/ethylbenzene (m/z 107) presented the most significant reduction (7%) amongst the aromatic hydrocarbons. We also observed a moderately increasing trend in hexenal (m/z 99; 10%), MEK (m/z 73; 6%) and toluene (m/z 93; 5%).
The estimated average OH concentration from the d-9 butanol decay was 1.4 × 106 molecules per cm3. This is a relatively low level, but it is not negligible. We also calculated the production rate of NO3 based on the NO2 and O3 concentrations in the absence of VOCs. In this experiment, within the first hour the production rate of NO3 radicals increased from 1.2 to 6.5 ppb h−1 (Fig. S2†). To evaluate the relative contribution of reactions with nitrate radical, ozone and OH to the oxidation of pellet emissions, we calculated the average lifetime of the VOCs with the largest decreasing trends: furfural, phenol, cresol, creosol, and monoterpenes (assumed to be α-pinene for this calculation). We used the reaction rate constants reported in Table S2.† For OH, we used its concentrations in the first hour after time zero. For the NO3 radical concentration, we assumed an average concentration of 8 × 108 molecules per cm3, as by Kodros et al.62 for a similar system.
For furfural, phenol and α-pinene, the average lifetimes for reactions with OH are greater than 6 hours (Table S3†). The corresponding lifetimes for reactions with NO3 are all less than half an hour for typical concentrations (0.14 h for phenol, 0.5 h for furfural, and 0.28 h for α-pinene), indicating that NO3 was the dominant oxidant of these VOCs in our experiments. Cresol and α-pinene have an average lifetime of more than a day and 1.3 h, respectively when reacting with ozone while the corresponding furfural reaction is very slow.79,80
Creosol and cresol display an average lifetime, for reaction with NO3, close to that of OH (2 h for creosol and 4 h for cresol), implying that their oxidation by the two oxidants was competitive. So, together with the NO3 reactions there were also some reactions with OH taking place, but their overall extent was secondary.
Fig. 5 shows the produced OA (including organic nitrate) in all dark aging experiments. The formed SOA ranged between 0.6 and 30 μg m−3, increasing the OA levels by 1–28% (Fig. 6a) after a few hours of exposure to NO3 radicals in the chamber. For the low RH experiments, the formed SOA after 4 h of oxidation ranged from 12–28% of the initial OA (11–30 μg m−3 increase). Dark experiments under humid conditions showed a 1–10% increase in OA, forming clearly less SOA (0.6–5 μg m−3) in comparison to low RH conditions (Fig. 6a). This indicates that dryer nights in “rich” biomass burning urban haze episodes may have a lot more SOA than under humid conditions.
Fig. 5 Produced OA (red bars) and organic nitrate (black bars) for the dark aging (1–6) and UV (7) experiments. The values correspond to diluted concentrations in the chamber. |
After the injection of NO2 and O3, both organic and inorganic nitrates increased. Organic nitrate increased in all experiments by 200–600%, while in the case of experiment 5 it increased up to 1000%, reaching values up to 1 μg m−3 (Fig. 6b). For the low RH set of dark aging experiments, the mass concentration of organic nitrate increased by 300–600% (corresponding to 0.7–2 μg m−3), while for the higher RH cases the produced secondary organic nitrate after 4 h ranged from 400 to 1000% (an increase of 0.9 to 1.6 μg m−3; Fig. 6b). Inorganic nitrate increased by 30–230% (0.6–2.7 μg m−3) in all experiments, with higher RH cases presenting an average increase of 80% and lower RH cases 170% (Fig. S3†). The enhancements of organic and inorganic nitrate aerosols are typical of dark aging due to the presence of NO3 radicals.
There was a minor increase in OA density (ranging from 3 to 7%) during the aging period. This increase was a bit higher in the case of higher RH experiments (4 to 7%; absolute change of 0.04 to 0.09 g cm−3) in comparison to the 3 to 4% (absolute change of 0.03 to 0.05 g cm−3) difference in low RH cases.
The theta angle between the fresh and aged OA spectra increased in all dark-aging experiments by 7–18°, in the 4 h of oxidation (Fig. 6c). The changes in the OA mass spectrum were smaller under low RH conditions. The theta angle changed around 6° in the first hour of dark oxidation and only 1–2 additional degrees during the next 3 hours.
For experiments 4–6 (elevated RH) the increase in the theta angle was almost twice (θ = 10–18°) at the end of the experiment (Fig. 6c), in comparison to low RH cases. Given the relatively low SOA formation at high RH, heterogeneous reactions in this system that oxidize the original OA appear to be important and deserve additional investigation. The theta angle between the aged spectra at t = 4 h for all experiments was also calculated (Table S4†). The theta angle between the aged spectra at t = 4 h for all experiments ranged between 4 and 8° in the case of low RH conditions (Exp. 1–3) and up to 20° for high RH cases (Table S4†). The average spectra for the dry and high RH cases, along with the corresponding deviations are shown in Fig. S5.†
For the high RH experiments in which the aged OA spectrum changed considerably, the levels of the CxHy+ family displayed a noticeable decrease (5%) compared to the fresh bbOA (Fig. 7). The fraction of the CxHyO+ family increased slightly (3%), while the CxHyOz+ and CxHyN+ families' contributions did not change significantly (change of 1%). The main differences between the fresh bbOA spectrum and that of elevated RH cases were found for m/z 28 and 44 which are more pronounced in the aged bbOA spectrum. The m/z 60 and 137 were lower in the aged bbOA spectra (Fig. 7b).
To quantify the evolution of OA composition, we examined the ratio of the OA mass signal at m/z 44 to m/z 60 (f44/f60) and the O:C. In the dark aging experiments after the injection of NO2 and O3 (precursors to the NO3 radical), an enhancement in f44/f60 by a factor of 1.5 to 2.5 was observed under both dry and high RH conditions (Fig. 6d). The dark aging of bbOA seems to be sensitive to RH suggesting a sensitivity of the aging process to water vapor and/or aerosol liquid water content. The enhancement for the low RH experiments was similar in all experiments, reaching its maximum of 1.5 after 30 min and increasing slowly during the rest of the experiments. The corresponding enhancement for high RH experiments increased throughout the experiment and was quite variable (1.5 to 2.5) (Table 2).
Species | Low RH | High RH | ||
---|---|---|---|---|
Fresh emissions | Dark aging | Fresh emissions | Dark aging | |
μg m− 3 | μg m− 3 | |||
Ammonium | 0.07 ± 0.06 | 0.05 ± 0.05 | 0.03 ± 0.03 | 0.05 ± 0.02 |
Sulfate | 0.22 ± 0.12 | 0.23 ± 0.10 | 0.70 ± 0.94 | 0.78 ± 1.04 |
Organics | 113.00 ± 82.83 | 130.20 ± 92.45 | 66.00 ± 10.58 | 66.89 ± 10.78 |
Nitrate | 1.10 ± 0.82 | 3.72 ± 2.41 | 2.90 ± 1.85 | 5.22 ± 2.00 |
Chloride | 0.23 ± 0.17 | 0.12 ± 0.12 | 0.47 ± 0.65 | 0.08 ± 0.09 |
BC | 4.07 ± 3.20 | 4.02 ± 3.12 | 4.23 ± 1.25 | 3.87 ± 1.22 |
ppb | ppb | |||
NO2 | 80.00 ± 26.46 | 46.15 ± 20.47 | 80.00 ± 36.06 | 37.97 ± 11.55 |
NO | 7.32 ± 2.60 | 3.02 ± 1.86 | 6.62 ± 2.49 | 3.26 ± 1.51 |
O3 | 85.00 ± 25.98 | 36.32 ± 7.11 | 78.33 ± 29.30 | 31.53 ± 9.29 |
m/z 42 (acetonitrile) | 16.95 ± 9.28 | 16.62 ± 9.41 | 10.08 ± 4.23 | 10.06 ± 3.90 |
m/z 57 (acrolein) | 6.76 ± 2.28 | 6.52 ± 2.08 | 5.87 ± 0.25 | 5.95 ± 0.20 |
m/z 73 (MEK) | 4.05 ± 0.71 | 4.22 ± 0.74 | 3.33 ± 0.43 | 3.51 ± 0.17 |
m/z 81 (monoterpenes/hexanal) | 3.65 ± 0.48 | 2.98 ± 0.23 | 3.09 ± 0.12 | 2.69 ± 0.06 |
m/z 93 (toluene) | 1.07 ± 0.46 | 1.15 ± 0.35 | 1.16 ± 0.21 | 1.29 ± 0.03 |
m/z 95 (phenol) | 4.98 ± 0.67 | 3.70 ± 0.31 | 4.50 ± 0.28 | 3.72 ± 0.19 |
m/z 97 (furfural) | 9.87 ± 3.54 | 5.93 ± 1.09 | 7.69 ± 0.28 | 5.97 ± 0.19 |
m/z 99 (hexenal) | 6.86 ± 1.80 | 7.36 ± 1.54 | 5.27 ± 0.23 | 5.69 ± 0.12 |
m/z 107 (xylenes) | 1.57 ± 0.55 | 1.36 ± 0.57 | 1.30 ± 0.07 | 1.38 ± 0.19 |
m/z 109 (cresol) | 8.58 ± 1.29 | 6.66 ± 0.45 | 9.29 ± 0.32 | 8.44 ± 0.56 |
m/z 115 (heptanal) | 7.19 ± 1.43 | 6.67 ± 0.60 | 5.46 ± 0.23 | 5.72 ± 0.34 |
m/z 135 (C10 aromatics) | 2.15 ± 0.60 | 1.68 ± 0.34 | 2.38 ± 0.55 | 2.60 ± 0.32 |
m/z 137 (monoterpenes) | 10.69 ± 1.21 | 9.18 ± 0.76 | 9.23 ± 0.17 | 9.13 ± 0.37 |
m/z 139 (creosol, methyl-guaiacol) | 13.53 ± 2.28 | 11.18 ± 0.59 | 11.40 ± 0.27 | 9.97 ± 0.24 |
m/z 149 (C11 aromatics) | 6.52 ± 0.98 | 6.91 ± 0.49 | 2.35 ± 0.50 | 2.49 ± 0.32 |
m/z 151 (4-vinylguaiacol) | 15.74 ± 2.44 | 13.25 ± 1.03 | 13.20 ± 0.30 | 13.02 ± 0.60 |
The O:C ratio increased in all experiments by 7–18% in 4 h (an absolute increase of 0.04–0.12). For experiment 5, which was performed at elevated RH (80%) but a relatively low concentration of NO2 and O3 (40 and 45 ppb, respectively), the corresponding increase in O:C (12%) was the lowest across the three high RH experiments. For the low RH experiments, the average O:C at 4 h was 0.59 ± 0.01 (mean ± SD), while for the higher RH cases, the corresponding value was 0.70 ± 0.06. The Van Krevelen (VK) diagram81 presents the relation between the H:C and O:C ratios. The OA components for the pellet-burning experiments shown here mostly fall outside the VK-triangle region (Fig. S6†). For low RH experiments the enhancement in aging metrics is accompanied by decreasing concentrations in most of the measured VOCs. The highest decrease was detected for furfural (m/z 97; 40 ± 14%), phenol (m/z 95; 26 ± 8%), cresol (m/z 109; 22 ± 3%), monoterpenes/hexanal (m/z 81; 20 ± 7%), creosol (m/z 139; 20 ± 10%) and monoterpenes (m/z 137; 14 ± 6%) (Fig. S4†). This is in agreement with previous studies as biomass-burning-related VOCs, such as furfural and monoterpenes (C10H16), can react with NO3 radicals, resulting in nighttime SOA production.73,82,83 Palm et al.84 suggested that nighttime NO3 oxidation of phenolic compounds in bbOA plumes leads to nitrophenolics, which considerably contribute to SOA production. A small increase was detected for hexenal (m/z 99; 8 ± 6%), MEK (m/z 73; 5 ± 2%) and toluene (m/z 93; 8 ± 2%).
In the high RH set of experiments, a reduction in the concentration for the majority of VOCs (Fig. S4†) was detected, but the decrease was lower than that during low RH experiments (in some cases even half). Furfural for example decreased to 22 ± 12%, followed by a decrease in phenol (17 ± 4%), monoterpenes (m/z 81; 13 ± 4%), creosol (13 ± 1%), and cresol (10 ± 3%). At the same time certain VOCs (e.g., toluene, xylene, and hexenal) appeared to increase a little, but most of these changes were within experimental error. A fraction of these changes may also be due to the production of the corresponding compounds from reactions of larger molecules.
In all cases O3 decreased to approximately 30 ppb (a decrease of 54 ± 7%) in the 4 h of oxidation, with the lowest decrease observed for the low oxidant cases. The NO2 followed the same trend as ozone decreasing to 45 ± 20%.
At the same time SOA formation of around 2 μg m−3 (2% increase in OA) was observed (Fig. S7a†). This is comparable to the formed SOA in dark experiment 5 and consistent with the low or no SOA mass formed by pellet emissions for the flaming phase under UV exposure in previous studies.7,29 This may be explained by the good burning conditions for the pellet stove but it may also be due to the specific feed used. Organic and inorganic nitrates did not increase under these daytime conditions (Fig. S7a†).
The O:C in this experiment increased to 0.63 (0.09 absolute increase or a 17% increase; Fig. S7c†) comparable to that of the high RH experiments under dark conditions. The aged OA spectrum changed in comparison to that of fresh emissions by a theta angle of 16°, similar to the 10–18° in the high RH dark-aging experiments. The fraction of m/z 60 (due to C2H4O2+, characteristic of levoglucosan which is used as a molecular marker in biomass burning) was f60 = 0.048 in the fresh bbOA spectrum and decreased to 0.035 in the corresponding aged spectrum.
After the 3 h of UV illumination the lights were turned off and the system remained dark for another two hours to monitor any change in the OA spectrum and O:C ratio. Both the θ angle and O:C did not change further.
The levels of most VOCs decreased after the UV lights were switched on. The highest decreases were observed for m/z 73, 81, 85, 87, 95, 97, 109, 139 and 151 (pinonaldehyde/4-vinylguaiacol) (Fig. S4†). The highest decrease (27%) was detected for m/z 139 (creosol and methyl-guaiacol) followed by MEK and furfural (m/z 73 and 97; −21% each) (Fig. S7d†). A slight increase (6–9%) was detected in m/z 31 (formaldehyde), 42 (acetonitrile), 47 (formic acid), 59 (acetone), 61 (acetic acid), 71 (methyl vinyl ketone (MVK) or methacrolein (MACR)) and 79 (benzene).
For the fresh emissions an average pH of 3.2 ± 0.4 was calculated for all dark experiments. By splitting the experiments into low and high RH sets, the pH for the low RH conditions was estimated to be equal to 3.1 ± 0.1, while for cases with elevated RH the pH was 3.4 ± 0.3 (Fig. 8). This is expected given that higher RH is associated with higher liquid water contents that tend to dilute aerosol acidity.69 The estimated pH changed after the ozone injection. For low RH cases, the pH increased to 3.9 ± 0.2 (a 0.8-unit increase; Table S8†) at t = 4 h, while at high RH the pH decreased to 3.1 ± 0.1 (0.3-unit decrease). In the reference experiment with UV lights (Exp. 7), the pH of the aerosol increased from 2.5 to 2.8 (0.3-unit increase).
The average OA spectra of fresh bbOA emissions from wood and pellet combustion had a theta angle of 20° (Fig. S9†) implying some similarity, but also significant differences. The main differences between the two spectra were found for the signals at m/z 29, 57, 60, 73, 77 (C6H5+), 124 (C6H4O3+), 137 and 167 (C9H11O3+). The peaks at m/z 29, 60 and 73 were much higher in the pellet spectra (almost three times in the case of m/z 60). The m/z 60 and 73 peaks are related to sugar anhydrides such as levoglucosan, mannosan and galactosan, which are produced during burning of biomass containing cellulose and hemicellulose and are considered tracers of bbOA.85,86 Previous studies have reported the percentages of m/z 60 for biomass burning to be in the range of 0.6% and 4.1% (ref. 87) which is consistent with the fresh olive bbOA (around 2% (ref. 33)). In the case of pellets the corresponding percentage is much higher and around 6%, out of the suggested range. This high peak at m/z 60 may be a possible tracer for pellet-related bbOA emissions. Other marker ions for biomass burning lignin-related monomers are the peaks at m/z 137 and 167,88 with the latter being visible only in the wood and not in the pellet spectrum.
The fresh pellet bbOA spectrum can also be compared to the corresponding bbOA spectra found in the AMS database (High-Resolution AMS Spectral Database)89 and other previous studies. The pellet spectrum was relatively similar (θ less than 20°) to the bbOA factors from campaigns in Fresno, Athens and Patras38,90 and shared some similarities with some of the spectra obtained during FLAME-I (Fire Lab at Missoula Experiment, Phase 1) such as the burning of Alaska core Tundra duff (θ = 22°), southern pine needles and mixed wood (both with θ of 25°). For the rest of the database spectra, the theta angle values exceeded 25° (Fig. S10†) reaching up to 50°. The angles with the smoldering bbOA spectra (not shown) exceeded 50°.
The average O:C or the fresh pellet bbOA was high and around 0.6. The corresponding O:C of fresh bbOA from logwood of Kodros et al.62 was in the range of 0.3–0.4, close to that in ambient studies, which usually report O:C values less than 0.4 for fresh bbOA emissions91 and higher than 0.7 for aged bbOA.92 The high O:C for pellets is associated with the high signal in m/z 60 (C2H4O2+) and is not due to m/z 44 (f44 was close to 0.04).
The triangle plot in Fig. 9 displays the evolution of pellet bbOA during nighttime and daytime aging in our experiments. During the daytime the OA changes chemically and after 4 h it approaches in this space the aged under dry conditions bbOA spectrum of Kodros et al.62 and also some of the OOA factors found in winter periods. For dark aging the role of RH is evident. Under dry conditions, the aged bbOA remains in the same region as the fresh OA (Fig. 9), despite the fact that production of SOA is observed. In contrast, at higher RH the OA changes and moves closer to the area where wintertime OOA factors reside.
Fig. 9 The oxidation pathway of the average dark dry (experiments 1–3; orange circles), average dark humid (experiments 4–6; blue circles), reference (Exp. 7 and 8; black) and UV (Exp. 9; red) experiments compared to ambient observations of OOA (pink squares), and bbOA (green squares) factors (ESI Table S6†). |
Dark oxidation for log wood burning emissions led to a significant enhancement in OA mass (up to 80%),62 which was much more than the increase reported here for pellets (up to 30%). The same picture applies also to the absolute change in the O:C. In this study the change in O:C varied between 0.04 and 0.12 (7–21% increase), while for the wood burning experiments the corresponding change was 0.09–0.23 (20–60% increase). This might be related to the higher initial O:C of the pellet OA. The final O:C after dark aging for both sources was close to 0.7, indicating that this might be the upper limit of oxidation under these conditions. In both studies, the experiments with the lowest increase in the O:C were those with the lowest levels of oxidants. Secondary nitrate aerosol was produced in all pellet and wood dark-aging experiments, with organic nitrate presenting a higher increase in both cases.
The dark aged bbOA spectra from pellets and wood log combustion were quite different. For low RH (10%) the spectra had a theta angle of 35° (Fig. S11a†) while for high RH it was a bit lower than 30° (Fig. S11b†). The high theta angles suggest that the aged OA spectra from the two sources can be potentially separated in ambient datasets by positive matrix factorization analysis or other source-apportionment techniques. The main differences between logs and pellets are found in AMS m/z 28 and 44, which are higher in the case of logwood emissions, and m/z 57, 60 and 73 which are higher in the aged pellet OA spectrum (Fig. S11†).
Phenol (m/z 95) was the major VOC consumed in the wood stove experiments while furfural (m/z 97) dominated for the pellets. Hexanal (m/z 83) was the major product detected in the wood dark aging experiments, while here it was mainly MEK (m/z 73) and hexenal (m/z 99).
The fresh pellet aerosol pH was 3.2, while Kodros et al.62 estimated a value of 2.8 for the wood bbOA pH. In the work by Kodros et al.,62 the pH of the aerosol remained constant and did not change significantly following dark oxidation. In contrast, in our study, the RH seems to play a major role, as for humid conditions the pH decreased by 0.3 units following dark oxidation (9% decrease) and increased by 0.8 units (26%) for low RH cases.
In all dark aging experiments furfural (m/z 97) was the measured VOC species that decreased the most, followed by monoterpenes/hexanal (m/z 81), phenol (m/z 95), cresol (m/z 109), monoterpenes (m/z 137) and creosol (m/z 139). These VOCs are expected to be the major contributors to the observed SOA formation.
Despite the relatively high SOA production at low RH, the bbOA AMS spectrum changed little and its O:C increased by only 7–8%. In contrast, at high RH even if there was little additional SOA formed the OA mass spectrum changed significantly and the aerosol became more oxidized. This finding suggests the importance of heterogeneous reactions that can change the composition of the bbOA without necessarily increasing its mass concentration significantly. Secondary nitrate aerosol was produced in all dark-aging experiments, with organic nitrate contributing on average 40% to total PM1 nitrate.
The fresh PM1 pellet emissions were dominated by organics (more than 90%), followed by BC and nitrate. The MCE found for the fresh bbOA (higher than 0.92) indicated flaming conditions, demonstrating good operation of the pellet stove and, thus, relatively efficient combustion conditions. The average fresh pellet bbOA spectrum resembles to some extent that of the one emitted by logs, with m/z at 57, 60, 73 and 167 presenting the main differences between the two spectra. The fresh bbOA at 70 μg m−3 consisted of extremely low-volatility (11%), low-volatility (5%), semi-volatile (68%) and intermediate-volatility (16%) compounds. Its estimated effective enthalpy of vaporization was equal to 77 ± 20 kJ mol−1. The fresh pellet bbOA displayed an average O:C ratio close to 0.6, which is associated with the high signal of m/z 60 (C2H4O2+).
Our results indicate significant differences in the aging of pellet and wood log burning emissions. This suggests that the corresponding emissions may need to be treated differently in chemical transport models that have so far lumped them together as residential biomass burning.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3ea00070b |
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