Secondary Organic Aerosol Formation Potential Research Articles

Comparison of the Yield and Chemical Composition of Secondary Organic Aerosol Generated from the OH and Cl Oxidation of Decamethylcyclopentasiloxane

Cyclic volatile methyl siloxanes (cVMS) that are emitted from industrial processes and consumer products often dominate the burden of volatile organic compounds (VOCs) in occupied spaces. cVMS may contribute to oxygenated VOC and secondary organic aerosol (SOA) formation following oxidation by gas-phase radicals in both indoor and outdoor source regions. Several recent studies examined the SOA formation potential of decamethylcyclopentasiloxane (D5) following exposure to hydroxyl radicals (OH) and found that this reaction generates SOA in high yield following multiple days of oxidative aging. Chlorine atoms (Cl) may compete with OH for the oxidative loss of D5 in indoor and outdoor source regions with active chlorine chemistry, but the SOA formation potential of D5 + Cl reactions has not been studied. Here, we characterized the yield and chemical composition of SOA generated from Cl oxidation of D5 in an oxidation flow reactor (OFR) under dry [relative humidity (RH) < 5%] and humid (RH = 40%) conditions and compared results to the yield and composition of SOA generated from OH oxidation of D5. D5 was oxidized using integrated OH and Cl exposures (OHexp and Clexp) ranging from 1.1 × 1012 to 8.2 × 1012 cm–3 s and from 1.6 × 1010 to 1.6 × 1012 cm–3 s, respectively. Like OH, Cl facilitated multistep SOA oxidative aging over the range of OFR conditions that were studied, with maximum SOA mass yields of 1.5 and 1.3 obtained following OH and Cl oxidation of D5 under humid conditions. These results suggest that indoor and outdoor source regions that are significantly influenced by chlorine chemistry may enhance the atmospheric SOA formation potential of D5.

Seasonal Characteristics of Volatile Organic Compounds in Seoul, Korea: Major Sources and Contribution to Secondary Organic Aerosol Formation

Volatile organic compounds (VOCs) are major pollutants that cause air pollution and are precursors that react in the air to produce secondary organic aerosol (SOA). This study attempted to elucidate the distribution characteristics of VOCs in the atmosphere of Seoul by measuring 34 types of VOCs in real time in the winter of 2020 and summer of 2021. The objectives of this research are as follows: (1) understand the characteristics of VOCs in Seoul and the difference between winter and summer compositions, (2) identify the main sources of VOCs in winter and summer, and (3) estimate the contribution of VOCs to the SOA formation potential in Seoul. Total VOC concentrations were found to be higher in summer (7.61 ± 4.22 ppb) than in winter (6.35 ± 4.11 ppb). To further specify the cause of the difference in major VOC components in winter and summer, a cause analysis was performed using the ratio between marker components, and an emission source analysis of VOCs was performed by applying the positive matrix factorization model (PMF). The source distribution of VOCs in Seoul was attributed to five factors: solvent usage, vehicle exhaust, industry/burning of fossil fuels, petrochemical industry, and road emission (winter)/gasoline-related (summer). The contribution of VOCs to SOA formation was estimated using the secondary organic aerosol formation potential. The results showed that toluene was the primary contributor to SOA formation in both winter and summer. In the summer, solvent usage containing high proportion of ethylbenzene and xylenes contributed more than twice as much to SOA formation compared to the winter.

A recent high-resolution PM2.5 and VOCs speciated emission inventory from anthropogenic sources: A case study of central China

Aiming to provide basic data support for the improvement of air quality in the study region, this study established the emission inventory and speciated emission inventory of PM2.5 and VOCs in Henan Province, and further estimated the ozone formation potential (OFP) and secondary organic aerosols formation potential (SOAFP) of VOCs to identify key species, priority sources and typical cities. The 2017-based emissions of PM2.5 and VOCs were 598 and 1079 kt, respectively. Industrial process, fugitive dust and biomass burning were the three major contributors to PM2.5, with a combined contribution of 79%, while industrial process, on-road mobile, solvent utilization and biomass burning were the four major contributors to VOCs emissions, with a combined contribution of 90%. Other unidentified species had the highest emissions, followed by carbonaceous components and inorganic elements and water-soluble ions. The total amount of OFP and SOAFP were 3482 and 81 kt. The species categories of VOCs that contributed large fractions to the emissions were alkanes, aromatic hydrocarbons and oxygenated VOCs, to the OFP were aromatic hydrocarbons, olefins, and oxygenated VOCs, and to the SOAFP were aromatic hydrocarbons and alkanes. Considering OFP and SOAFP together, industrial process, solvent utilization, on-road mobile and biomass burning are the key emission sources to control. The overall spatial distribution showed that PM2.5 and VOCs emissions were relatively low in the southwest and southeast of Henan province, while emissions were high in densely populated, industrial, agricultural and transportation developed areas, and the spatial distribution characteristics of OFP and SOAFP were similar to those of VOCs emissions.

Improving VOC control strategies in industrial parks based on emission behavior, environmental effects, and health risks: A case study through atmospheric measurement and emission inventory

Industrial parks have a very important impact on regional economic development, but the extremely complex and relatively concentrated volatile organic compound (VOC) emissions from industrial parks also result in it being difficult to control VOCs. In this study, we took a large integrated industrial park in the upper reaches of the Yangtze River as an example, conducted a 1-year monitoring campaign of ambient air VOCs, and established a speciated VOC emission inventory based on the measured chemical profiles of the key industries. The comprehensive control index (CCI) of 125 VOCs was evaluated using the entropy weighting method based on comprehensive consideration of three aspects, namely, emission behavior, environmental effects, and health risks of VOCs, to identify priority VOC species and their key sources for VOC control in industrial parks. The total estimated VOC emissions in the industrial park in 2019 were 6446.96 t. Steel production, sewage treatment, natural gas chemical industry, pharmaceuticals, and industrial boilers were the main sources of VOC emissions. In terms of VOC components, halocarbons, aromatics, and OVOCs were the largest groups of VOCs emitted from the industrial park, accounting for 73.75 % of the total VOC emissions. Using the entropy weighting method, we evaluated the index weights of five parameters: emissions, ozone formation potential, secondary organic aerosol formation potential, hazard quotient, and lifetime cancer risk. Based on the CCI, five control levels for VOC species were further established. The VOC species in Level I and Level II, which contain species such as naphthalene, 2-chlorotoluene, benzene, acrolein, and chloroform, should be considered as extremely important priority control species. These results serve as a reference for the development of precise control strategies for VOCs in industrial parks.

Spatio-temporal variations, ozone and secondary organic aerosol formation potential, and health risk assessment of BTEX compounds in east of Azerbaijan Province, Iran

The present study aims to investigate the Spatio-temporal variation of benzene, toluene, ethylbenzene, and xylenes (BTEX), and their health risk assessments in the urban ambient air of Maragheh, Iran. Air samples were collected in the morning and evening from 15 points with low, medium, and high traffic. BTEX concentration in high traffic areas was 5.16 times higher than in low traffic areas. The highest mean concentration of BTEX was observed during the winter due to emissions from house heating, atmospheric inversion, and declined dilution of pollutants. The annual mean concentrations (lowest and highest concentration) of benzene, toluene, ethylbenzene, xylene and BTEX were 2.29 ± 1.07 (0.42–13.99), 5.52 ± 2.33 (1.37–29.45), 0.8 ± 0.32 (0.37–3.84), 4.47 ± 1.89 (1.48–29.79), and 12.75 ± 5.25 (3.65–74.07) μg.m−3, respectively. Moreover, it was observed that heavy vehicular traffic and lack of hydroxyl radicals (%OH) resulted in higher BTEX concentrations during rush hours compared to non-rush hours. The inhalation lifetime cancer risk (ILCR) for benzene and ethylbenzene in three age groups of birth to <1 year, 2 to <18, and 19 to <70 years was estimated to be in the range of 2.63 × 10−7–5.14 × 10−6 and 1.29 × 10−8–2.53 × 10−7, respectively, indicating that the ILCR value of benzene children and adults exceeded the recommended values.

Volatile organic compounds in ambient air of a major Asian port: spatiotemporal variation and source apportionment.

This study investigated the spatiotemporal variation and source characteristics of volatile organic compounds (VOCs) in Kaohsiung Harbor, one of the busiest ports in the world. The VOCs' potential to form ozone (O3) and secondary organic aerosols (SOAs) was also examined. The temporal variation was studied in February, May, July, and November of 2020, while the spatial distribution was investigated in the export processing zone (KEPZ) and at the two port entrances (E1 and E2). The most polluted month in the harbor was November (37.7 ± 12.6ppbv), while the most polluted site was the industrial area (KEPZ). A significant positive correlation was found between VOCs and O3 (r = 0.985). Meanwhile, a moderate positive correlation (r = 0.449) was observed between VOCs and secondary organic aerosol formation potential (SOAFP), mainly affected by the concentration of toluene in the study area. The diagnostic ratios indicated that the air parcels in the site were "fresh," and three possible ambient sources of VOC were identified by the positive matrix factorization (PMF): industrial emissions (53.6%), freight transport emissions (29.6%), and others (17.7%). The study highlights the current state of VOCs and their potential sources in the port city of Kaohsiung, which can be used to enhance the strategies for regulating and controlling industrial activities and improving air pollution control measures to reduce VOC emissions.

Analysis of VOCs Emitted from Small Laundry Facilities: Contributions to Ozone and Secondary Aerosol Formation and Human Risk Assessment.

Volatile organic compounds (VOCs) emitted to the atmosphere form ozone and secondary organic aerosols (SOA) by photochemical reactions. As they contain numerous harmful compounds such as carcinogens, it is necessary to analyze them from a health perspective. Given the petroleum-based organic solvents used during the drying process, large amounts of VOCs are emitted from small laundry facilities. In this study, a laundry facility located in a residential area was selected, while VOCs data emitted during the drying process were collected and analyzed using a thermal desorption-gas chromatography/mass spectrometer (TD-GC/MS). We compared the results of the solvent composition, human risk assessment, contribution of photochemical ozone creation potential (POCP), and secondary organic aerosol formation potential (SOAP) to evaluate the chemical species. Alkane-based compounds; the main components of petroleum organic solvents, were dominant. The differences in evaporation with respect to the boiling point were also discerned. The POCP contribution exhibited the same trend as the emission concentration ratios for nonane (41%), decane (34%), and undecane (14%). However, the SOAP contribution accounted for o-xylene (28%), decane (27%), undecane (25%), and nonane (9%), thus confirming the high contribution of o-xylene to SOA formation. The risk assessment showed that acrylonitrile, carbon tetrachloride, nitrobenzene, bromodichloromethane, and chloromethane among carcinogenic compounds, and bromomethane, chlorobenzene, o-xylene, and hexachloro-1, 3-butadiene were found to be hazardous, thereby excessing the standard value. Overall these results facilitate the selection and control of highly reactive and harmful VOCs emitted from the dry-cleaning process.

Effects of soil drought and nitrogen deposition on BVOC emissions and their O3 and SOA formation for Pinus thunbergii

Soil drought and nitrogen (N) deposition can influence the biogenic volatile organic compound (BVOC) emissions and thereby their ozone (O3) and secondary organic aerosol (SOA) formation. This study addressed their single and combined effects on BVOC emissions of Pinus thunbergii by laboratory simulation experiments. The results showed that light drought (LD, 50% soil volumetric water content (VWC)) stimulated isoprene, monoterpene, sesquiterpene, and total BVOC emissions, while moderate drought (MD, 30% and 40% VWC) and severe drought (SD, 10% and 20% VWC) inhibited their emissions (except for sesquiterpene in 20% VWC). N deposition decreased other VOC emissions and increased isoprene and sesquiterpene emissions. Total BVOCs and monoterpene were stimulated in low N deposition (LN, 2 g N/(m2·yr)) and inhibited in moderate (MN, 5 g N/(m2·yr)) and high N deposition (HN, 10 g N/(m2·yr)). Under combined treatment of soil drought and N deposition, total BVOC, monoterpene, and other VOC emissions were inhibited, sesquiterpene had no significant change, and isoprene emission was inhibited in MD combined treatment but promoted in SD. The O3 formation potential (OFP) and SOA formation potential (SOAP) from the changed BVOC emissions were calculated, OFP and SOAP of BVOC emissions and their compositions varied significantly among the treatments. Our study provided theoretical basis for assessing the impact of climate change and atmospheric pollution on BVOC emissions and their contribution to the formation of secondary atmospheric pollution.

Characteristics, secondary transformation and odor activity evaluation of VOCs emitted from municipal solid waste incineration power plant

Volatile organic compounds (VOCs) emitted from municipal solid waste incineration power plant (MSWIPP) plays a significant role in the formation of O3 and PM2.5 and odor pollution. Field test was performed on four MSWIPPs in an area of the North China Plain. Nonmethane hydrocarbons (NMHCs) and 102 VOCs were identified and quantified. Ozone formation potential (OFP), secondary organic aerosol formation potential (SOAFP), and odor activity of the detected VOCs were evaluated. Results showed that the average concentration of NMHCs and VOCs were 1648.6 ± 1290.4 μg/m3 and 635.3 ± 588.8 μg/m3, respectively. Aromatics (62.1%), O–VOCs (16.0%), and halo hydrocarbons (10.0%) were the main VOCs groups in the MSWIPP exhaust gas. VOCs emission factor of MSWIPP was 2.43 × 103 ± 2.27 × 103 ng/g-waste. The OFP and SOAFP of MSWIPP were 960.18 ± 2158.17 μg/m3 and 1.57 ± 3.38 μg/m3, respectively. Acrolein as the dominant VOC species was the major odor contributor with a percentage of odor contribution of 65.9%. Benzene and 1,2,4-trimethylbenzene as the dominant VOC species were the main contributors of O3 formation potentials, in which 1,2,4-trimethylbenzene was also the main contributors of SOA formation potential.

Characteristics, sources of volatile organic compounds, and their contributions to secondary air pollution during different periods in Beijing, China

Continuous measurements of volatile organic compounds (VOCs), ozone (O3), fine particulate matter (PM2.5), and related parameters were conducted between April 2020 and March 2021 in Beijing, China, to characterize potential sources of VOCs and their impacts on secondary organic aerosols (SOAs) and O3 levels. The annual average mixing ratio of VOCs was 17.4 ± 10.1 ppbv, with monthly averages ranging from 11.6 to 25.2 ppbv. According to the empirical kinetic modeling approach (EKMA), O3 formation during O3 season was “VOCs-limited”, while it was in a “transition” regime during O3 pollution episodes. In the O3 season, higher ozone formation potential (OFP) of m/p-xylene, o-xylene, toluene, isopentane, and n-butane were evident during O3 pollution episodes, in line with the increasing contributions of solvent usage and coating, as well as gasoline evaporation to OFP obtained through a matrix factorization model (PMF). Aromatics contributed the most to the secondary organic aerosol formation potential (SOAFP). In the non-O3 season, the contribution of vehicle exhaust to SOAFP elevated on hazy days, thereby revealing the importance of traffic-derived VOCs for PM2.5 pollution. Our results indicate that the prior control of different VOC sources should vary by season, thereby facilitating the synergistic control of O3 and PM2.5 in Beijing.

Characteristics of volatile organic compounds and secondary organic aerosol pollution in different functional areas of petrochemical industrial cities in Northwest China

The aim of this study was to better understand the characteristics of volatile organic compounds (VOCs) and secondary organic aerosol (SOA) pollution in different functional areas of petrochemical industrial cities. In Lanzhou, a typical petrochemical industrial city in Northwest China, with the use of an Integrated Atmospheric Mobile Monitoring Vehicle (IAMMV), various real-time online monitoring instruments, including a VOC monitoring instrument (TH-300B) and single-particle aerosol mass spectrometer (SPAMS), were used in combination. These instruments were employed to determine PM2.5, VOCs and other factors at monitoring sites in Xigu (XG) and Chengguan (CG) districts in September 2020 and 2021, respectively. The results revealed that during the monitoring period, the average VOC concentrations at the XG and CG monitoring sites were 102.3 and 35.8 ppb, respectively. Benzene (45.58 %) and toluene (24.47 %) significantly contributed to the SOA formation potential at the XG site. M/P-xylene (27.88 %) and toluene (23.64 %) more notably contributed to the SOA formation potential at the CG site. The PM2.5 mass concentration at the XG site (24.1 μg·m−3) was similar to that at the CG site (21.2 μg·m−3), but the proportion of particulate matter components greatly differed. The proportion of organic carbon (OC) at the XG site (19.00 %) was higher than that at the CG site (9.97 %). The number of particles containing C2H3O+ (m/z = 43) accounted for 36.96 % and 15.41 % of the total particles at the XG and CG sites, respectively. The mixing ratios of OC and hybrid carbon (OCEC) with C2H3O+ (m/z = 43) were 0.81 and 0.53, respectively, at the XG site and reached only 0.48 and 0.25, respectively, at the CG site. The secondary ageing degree of particles in XG district was high. These results could provide a reference for ambient air quality improvement and the formulation of governance measures in different functional areas of petrochemical industrial cities.

Determining an optimal control strategy for anthropogenic VOC emissions in China based on source emissions and reactivity

An evidence-based control strategy for emission reduction of VOC sources can effectively solve the regional PM2.5 and O3 compound pollution in China. We estimated the anthropogenic VOC emission inventory in China in 2018 and established a source profile database containing 129 sources based on localized detection and the latest research results. Then, the distribution of the ozone formation potential (OFP) and secondary organic aerosol formation potential (SOAFP) for emission sources was analyzed. Moreover, priority control routes for VOC emission sources were proposed for different periods. Anthropogenic VOC emissions in China reached 27,211.8 Gg in 2018, and small passenger cars, industrial protective coatings, biomass burning, heavy trucks, printing, asphalt paving, oil storage and transportation, coking, and oil refining were the main contributors. Industrial protective coatings, small passenger cars, and biomass burning all contributed significantly to OFP and SOAFP. Priority in emission reduction control should be given to industrial protective coatings, small passenger cars, heavy trucks, coking, printing, asphalt paving, chemical fibers, and basic organic chemical sources over the medium and long term in China. In addition, the priority control route for VOC emission sources should be adjusted according to the variations in VOC emission characteristics and regional differences, so as to obtain the maximum environmental benefits.

Quantification of enhanced VOC emissions from fireworks

Fireworks are widely used in celebrations worldwide. The effects of fireworks on the physicochemical characteristics of atmospheric particles are well documented. However, the influence of firework burning on ambient volatile organic compound (VOC) emissions remains unclear. To determine the impact of firework-burning events on VOC emissions, ambient VOCs were measured at a receptor site on the Fenwei Plain during the Chinese Spring Festival period. Firework-burning plumes were identified by using potassium ions (K+) as tracers, and twenty VOC species were obtained as firework tracers. The emission ratios of the VOC species relative to K+ were in a range of 5.40 × 10−3–1.41 μg m−3/μg m−3 and were first estimated through the linear fitting method and source-tracer-ratio method. The VOC contributions of firework burning during the Lantern Festival (31.7 ± 8.3%) were higher than the levels during the Chinese New Year (28.6 ± 7.5%). The daytime net ozone (O3) formation rates during the Spring Festival and Lantern Festival increased by 11.4% and 15.2%, respectively, on average due to firework emissions. Secondary organic aerosol formation potential (SOAP) increased by 18.2% and 34.1% on average, respectively. These results can provide the source tracers of fireworks, and can subsequently help assess their impact on regional air quality and public health.

Intermediate‐Volatility Organic Compounds Observed in a Coastal Megacity: Importance of Non‐Road Source Emissions

AbstractIntermediate‐volatility organic compounds (IVOCs) are among the most important precursors to secondary organic aerosol (SOA), yet their sources and contributions to SOA in ambient air are poorly constrained. In this study, IVOCs were collected with sorption tubes in a coastal city in southern China during September–October 2019 and were analyzed by gas chromatography‐mass selective detector after thermo‐desorption. The measured average concentration of IVOCs was 25.0 ± 0.95 μg m−3 (mean ± 95% C.I.), and residual unresolved complex mixtures shared 79.8% ± 1.91% of IVOCs. The estimated SOA production, even only from speciated IVOCs and unspeciated branch‐alkane IVOCs, reached 2.44 ± 1.46 μg m−3, approximately five times that from VOCs during the photochemically active period (12:00–15:00 local time). Based on the positive matrix factorization model with a photochemical‐age‐based parameterization, diesel‐related emission was the largest contributor (46.6%) of IVOCs, followed by ship emission (23.0%), gasoline exhaust (16.8%), and biomass/coal burning (13.6%). Non‐road diesel engines accounted for a dominant part in diesel‐related emission. Ship emission was found to contribute SOA formation potentials (SOAFPs) comparable to that of diesel‐related emission, while biomass/coal burning showed higher SOAFPs than gasoline exhaust. Our results revealed that non‐road sources, such as ship emission, non‐road diesel engines, and biomass/coal burning contributed substantially to IVOCs, and will be of greater importance in producing ambient SOA with the increasingly stringent control on emissions from on‐road vehicles.

Measurement report: Ambient volatile organic compound (VOC) pollution in urban Beijing: characteristics, sources, and implications for pollution control

Abstract. The increasing ozone (O3) pollution and high fraction of secondary organic aerosols (SOA) in fine particle mass has highlighted the importance of volatile organic compounds (VOCs) in air pollution control. In this work, four intensive field measurements of VOCs during winter of 2018 (from 1 December 2018 to 17 January 2019), spring (15 April to 27 May), summer (17 June to 13 July), and autumn (22 September to 27 November) of 2019 were conducted at an urban site in Beijing to characterize VOC sources and their contributions to air pollution. The total mixing ratio of the 95 quantified VOCs (TVOC) observed in this study ranged from 5.5–118.7 ppbv with the mean value of 34.9 ppbv. Alkanes, OVOCs, and halocarbons were the dominant chemical groups, accounting for 75 %–81 % of the TVOC across the sampling months. The molar ratios of VOCs to NOx indicated that O3 formation was limited by VOCs during the whole sampling period. Positive matrix factorization (PMF) analysis showed that diesel vehicle exhaust, gasoline vehicle exhaust, and industrial emissions were the main VOC sources during both the O3-polluted and PM2.5-polluted months. On the basis of O3 formation impact, VOCs from fuel evaporation and diesel exhaust, particularly toluene, xylenes, trans-2-butene, acrolein, methyl methacrylate, vinyl acetate, 1-butene, and 1-hexene, were the main contributors, illustrating the necessity of conducting emission controls on these pollution sources and species to alleviate O3 pollution. Instead, VOCs from diesel exhaust as well as coal and biomass combustion were found to be the dominant contributors to secondary organic aerosol formation potential (SOAFP), particularly the VOC species of toluene, 1-hexene, xylenes, ethylbenzene, and styrene, and top priority should be given to these for the alleviation of haze pollution. This study provides insights for the government to formulate effective VOC control measures for air pollution in Beijing.

Distribution characteristics, source apportionment, and chemical reactivity of volatile organic compounds in two adjacent areas in Shanxi, North China

To determine the pollution characteristics, source apportionment, and chemical reactivity of volatile organic compounds (VOCs) in two adjacent areas, VOC samples were collected using 3.2-L stainless steel canisters between 2017 and 2018 in Taiyuan and Yuci areas. The concentrations of 48 VOCs were determined using a gas chromatography-mass selective detector/flame ionization detector. The average concentrations of the 48 VOCs (total VOCs [TVOCs]) in the Taiyuan and Yuci areas were 30.09 and 24.08 ppbv, respectively; the highest concentrations were recorded for ethane, which accounted for 21.40% and 25.49% of the TVOCs detected in the Taiyuan and Yuci areas, respectively. Alkanes accounted for the highest proportion of the TVOCs, followed by alkenes, alkynes, and aromatics. Through positive matrix factorization, six source categories were identified in Taiyuan and Yuci, namely gasoline evaporation (24.38%), petrochemical industrial sources (15.46%), biogenic emissions and LPG usage (8.75%), combustion sources (28.33%), solvent use (12.95%), and vehicle exhaust (10.13%). The backward trajectory and weighted potential source contribution function analysis results indicated that Taiyuan and Yuci were potential source areas for each other in September, and that Taiyuan was the potential source area of Yuci in November and December. Among the TVOCs detected in the Taiyuan and Yuci areas, alkenes contributed the most to ozone formation potential (OFP), followed by aromatics and alkanes; alkynes contributed the least to OFP. Aromatics contributed the most to secondary organic aerosol formation potential (SOAFP), accounting for 92.80% and 92.37% of the SOAFP in the Taiyuan and Yuci areas, respectively. These results indicate that the TVOCs in the Taiyuan and Yuci areas must be controlled, particularly aromatics with high SOAFP and alkenes with high OFP. Our results help to clarify the migration, transformation, and sources of ambient VOCs in adjacent areas; they also provide fundamental data on pollution control and the prevention of regional organic air pollution.

Atmospheric gaseous aromatic hydrocarbons in eastern China based on mobile measurements: Spatial distribution, secondary formation potential and source apportionment

Monocyclic aromatic hydrocarbons (MAHs) and polycyclic aromatic hydrocarbons (PAHs) are both well known as hazardous air pollutants and also important anthropogenic precursors of tropospheric ozone (O3) and secondary organic aerosols (SOA). In recent years, there have been intensive studies covering MAHs emission from various sources and their behavior under stimulated photochemical conditions. Yet in-situ measurements of PAHs presence and variations in ambient air are sparse. Herein we conducted large geometrical scale mobile measurements for 16 aromatic hydrocarbons (AHs, including 7 MAHs and 9 PAHs) in eastern China between October 27 and November 8, 2019. This unique dataset has allowed for some insights in terms of AHs concentration variations, accompanying chemical composition, source contributions and spatial distributions in eastern China. In general, AHs showed a clear concentration variability between the south and the north of the Yangtze River Delta (YRD). The concentrations of PAHs were approximately 9% of AHs, but contributed 23% of SOA formation potential. Source apportionment via positive matrix factorization (PMF) model revealed that industrial processes as the largest source (44%) of observed AHs, followed by solvent usage (21%), vehicle exhaust (19%), coal combustion (11%) and coking processes (6%). In the perspective of PAHs sources, coal combustion emissions were identified as the dominating factor of a share of 41%–52% in eastern China. Our findings complemented the simultaneously monitoring information of PAHs and MAHs in eastern China, revealed the importance of PAHs to SOA formation and highlighted the necessity of formulating strategies to reduce emissions from anthropogenic sources and reduce risks to human health.

Characteristics and Reactivity of VOCs in a Typical Industrial City in Summer

To investigate the ambient pollution caused by volatile organic compounds (VOCs) in a typical industrial city in summer, the characteristics and chemical reactivity from VOCs and the causes of ozone (O3) pollution were analyzed using online VOCs measurements during polluted and non-polluted periods in Zibo city in July 2020. The results showed that the average hourly concentration of total volatile organic compounds (TVOC) during the polluted period[(50.6±28.3)] μg·m-3 was 32.5% higher than that during the non-polluted period[(38.2±24.9) μg·m-3]. The contribution of all VOCs categories were as follows:alkanes>aromatics>alkenes>alkynes, and the diurnal averages of TVOC and O3 concentrations were opposite during the polluted and non-polluted period. Ozone formation potential (OFP),·OH radical loss rate (L·OH), and secondary organic aerosol formation potential (SOAp) during the polluted period were higher than those during the non-polluted period. Alkenes contributed most to OFP and L·OH, whereas aromatics contributed most to SOAp. The tendency of the diurnal average of OFP and SOAp was overall consistent with that of TVOC. The priority species of OFP, L·OH, and SOAp were alkenes and aromatics. The VOCs/NOx method was applied to identify the O3-VOC-NOx sensitivity during the polluted and non-polluted periods, and the results showed that the photochemical regimes were VOCs-limited and transition regions. In addition, the smog production model (SPM) was employed to identify the O3 formation regime, and the results showed that those during the polluted period were identified as VOCs-limited and transition regions from 08:00 to 16:00, whereas the non-polluted period was mainly considered to be VOCs-limited. To mitigate the O3 pollution in summertime, the synergistic control of VOCs (especially alkenes and aromatics) and NOx emissions should be enforced.

Levels, ozone and secondary organic aerosol formation potentials of BTEX and their health risks during autumn and winter in the Guanzhong Plain, China

Levels, ozone and secondary organic aerosol formation potentials of BTEX and their health risks during autumn and winter in the Guanzhong Plain, China

Characteristics of VOCs and their contribution to O3 and SOA formation across seasons over a metropolitan region in India

Understanding and quantifying the influence of volatile organic compounds (VOCs) on ozone and secondary organic aerosol formation is essential for better prediction/estimation of these products. A total of 9 VOCs along with surface ozone were measured during the year 2019 at Pune (India) location. The ozone formation potential (OFP) and secondary organic aerosol formation potential (SOAFP) estimations are compared for 2 methods-using measured VOC concentrations and using their photochemical initial concentrations (PIC). The OFP and SOAFP estimated based on the measured VOC concentrations provide an incomplete understanding of these 2 formation processes. This is mainly because measured VOCs don't account for the photochemical losses that compounds undergo from the source to the receptor. The PIC values of VOCs have been estimated in this study to highlight the importance of considering the photochemical losses. For example, the PIC value of highly reactive compound, isoprene, was found to be 152% higher (1.48 ppbv) than its measured value (0.59 ppbv). The resultant total OFP estimate based on PIC values of all the VOCs was found to be 53.30 ± 35.02 ppbv as compared to 45.99 ± 29.35 ppbv obtained from measured VOCs. Based on k-means clustering analysis, it was found that the highest ozone formation was favored under transition regime chemistry when PIC values were considered. The average total SOAFP based on PIC values was found to be 1.32 ± 1.40 ppbv, while it was 1.17 ± 1.18 ppbv for measured VOCs. The aromatics contributed to over 90% of total SOAFP estimated for the region.