Ozone Formation Potential Research Articles

Characteristics and Source Apportionment of Ambient Volatile Organic Compounds in Shijiazhuang High-tech Industrial Development Zone in Autumn

Utilizing the online monitoring data of volatile organic compounds （VOCs） and ozone （O3） in the Shijiazhuang high-tech industrial development zone during October 2020, the pollution characteristics of VOCs were analyzed. Subsequently, ·OH estimation, secondary organic aerosol formation potential （SOAP）, and ozone formation potential （OFP） were applied to assess the chemical reactivity of VOCs. Additionally, the source apportionment was identified using the positive matrix factorization （PMF） model. The results revealed that the hourly φ[total VOCs （TVOCs）] were （11-281）×10-9, and the components were ranked by volume fraction in the following order： oxygenated volatile organic compounds （OVOCs） （60.83%）, alkanes （19.98%）, halohydrocarbons （5.64%）, aromatics （5.91%）, alkenes （4.83%）, and alkynes （2.48%）. Although the VOC concentration levels posed negligible non-carcinogenic risks to human health, benzene and ethylbenzene presented carcinogenic risks. The m/p-xylene to ethylbenzene ratio （X/E） varied from 2.5 to 3.4, indicating short-range transport of fresh air masses. Based on the X/E value, the ·OH concentration was 1.75×106 molecule·cm-3, and the ·OH exposure from 07：00 to 14：00 was calculated as 3.77×1010 molecule·s·cm-3. Aromatics played a dominant role in SOA, with a contribution rate as high as 93.35%, while alkenes dominated O3 formation, with the OFP contribution rate reaching up to 46.79%. By applying the PMF model, five major VOC sources were identified, including industrial sources （37.20%）, process flow and solvent use （33.80%）, vehicle and oil/gas evaporation sources （15.47%）, combustion sources （8.03%）, and plant emissions （5.50%）. Industrial and process emissions emerged as the primary contributors to VOCs in the ambient air of the high-tech zone, necessitating targeted control measures within this region.

Fugitive VOCs emitted by pharmaceutical wastewater treatment plant: Pollution characteristic, odor activity, ozone formation potential and health risk

Fugitive VOCs emitted by pharmaceutical wastewater treatment plant: Pollution characteristic, odor activity, ozone formation potential and health risk

In-house green hydrogen production for steelmaking decarbonization using steel slag as thermal energy storage material: A life cycle assessment

Steel production is a highly energy-intensive industry, responsible for significant greenhouse gas emissions. Electrification of this sector is challenging, making green hydrogen technology a promising alternative. This research performs a thermodynamic analysis of green hydrogen production for steel manufacturing using the direct reduction method. Four solid oxide electrolyzer (SOE) modules replace the traditional reformer to produce 2.88 kg/s of hydrogen gas, serving as a reducing agent for iron pellets to yield 30 kg/s of molten steel. These modules are powered by 37,801 photovoltaic units. Additionally, a thermal storage system utilizing 1342 tons of steel slag stores waste heat from Electric Arc Furnace (EAF) exhaust gases. This stored energy preheats iron scraps charged into the EAF, reducing energy consumption by 5 %. A life cycle assessment, conducted using open LCA software, reveals that the global warming potential (GWP) for the entire process, with a capacity of 30 kg/s, equates to 93 kg of CO2. The study also assesses other environmental impacts such as acidification potential, ozone formation, fine particle formation, and human toxicity. Results indicate that the EAF significantly contributes to global warming and fine particle formation, while the direct reduction process notably impacts ozone formation and acidification potential.

Chemical characteristics of BTEX, Formaldehyde and Trace gases: concentration, ozone formation potential and source apportionment at a campus site of Agra.

Benzene, toluene, ethylbenzene, xylenes (BTEX) and formaldehyde (HCHO) impact the environment and human health due to their deleterious effect and are of great concern. In the present study, diurnal and seasonal trend of BTEX and HCHO along with trace gases are reported. BTEX samples were collected by activated charcoal tubes and analysed by Gas Chromatograph coupled with Mass Spectrometer and Flame Ionization Detector (GC-MS/FID) and formaldehyde sampling was done by impinger method and analysed by UV-Visible Spectroscopy. Summation BTEX varied from 50.3 to 188.3µgm-3 (average = 74.8 ± 31.8µgm-3). Amongst all species, toluene was the most abundant. Highest levels of BTEX, NOx and CO were observed in winter (96.4 ± 39.1µgm-3, 11.9 ± 7.8ppb and 540.8 ± 402.0ppb respectively) probably due to enhanced local emissions, stagnant weather conditions resulting in dilution and dispersion of pollutants and weak photochemical removal. Lower values are seen during monsoon (58.6 ± 25.4µgm-3, 7.6 ± 6.1µgm-3 and 149.8 ± 68.7µgm-3) as a consequence of rain showers and washout effect leading to clean atmospheric conditions. Further, ozone forming potential (OFP) BTEX was determined based on their reactivity with OH˙radical and concentration. Toluene (90.9µgm-3) was the largest contributor to ozone formation, whereas benzene (9.1µgm-3) was the lowest. Source apportionment of BTEX was determined based on estimation of diagnostic ratios, correlations and positive matrix factorization (PMF) analysis and revealed emissions from vehicles was the main source. Air mass back trajectory analysis for different seasons shows the impact of long-range during the summer season and localized air masses during winter season. The results of the current study provide a better understanding of OFP and sources of BTEX and HCHO to formulate effective pollution management.

Onboard measurements of organic vapor emissions from river vessels under various operational conditions

The emission factors and characteristics of pollutants from river vessels are critical for understanding the environmental impact of ship emissions, particularly in inland waterways. However, research gaps remain regarding emissions of volatile organic compounds (VOCs) and intermediate-volatility organic compounds (IVOCs) from river vessels. In this study, we collected and analyzed organic vapor emissions, including non-methane hydrocarbon (NMHCs), oxygenated volatile organic compounds (OVOCs) and IVOCs, from three river vessels under different operating conditions. The results show that the average emission factors of NMHCs, and IVOCs from river vessels are significantly higher than those from ocean-going vessels. Inland waterways’ proximity to residential areas increases the risk of pollutant transport to urban environments, heightening the importance of managing river vessel emissions. Notably, older auxiliary engines displayed higher organic vapor emissions compared to main engines, underscoring the need for better control measures for aging engines. By analyzing the emission characteristics of organic vapors from river vessels, it was found that, unlike other pollution sources where C12 n-alkanes are the major contributors of IVOCs, the contributions of C12-C15 n-alkanes in river vessel exhaust are similar, with C14 n-alkane having the highest contribution. OVOCs constituted more than 50% to ozone formation potentials of organic vapors, while IVOCs were responsible for over 90% of the secondary organic aerosol (SOA) formation. Given these findings, targeted efforts to reduce OVOCs and IVOCs emissions from river vessels should prioritized to mitigate their environmental impact.

Heatwave-amplified atmospheric oxidation in a multi-province border area in Xuzhou, China

Ozone formation is closely tied to emissions of precursors, meteorological conditions, and atmospheric chemistry. In June 2024, Xuzhou City, located at the intersection of Jiangsu, Shandong, Henan, and Anhui provinces in East China, experienced a series of ozone pollution events. The continuous pollution episodes were characterized by consistently high levels of ozone, with daytime peaks reaching 130 ppb. By combining observations of atmospheric oxidation and the use of the Observation-Based Model model, it was determined that the pollution was the result of a “heatwave-ozone” co-occurring extreme event triggered by elevated temperatures, low humidity, and intense radiation. The heatwave led to increased emissions of VOCs from both natural and human-related sources, with more pronounced contribution from Bio-alkenes and OVOCs. This, in turn, resulted in higher levels of oxidizing agents and ozone formation potential, exacerbating the co-occurrence of heatwaves and ozone extremes. Sensitivity tests on enhanced controls showed that reducing NOx had a significant adverse effect on ozone levels, whereas reducing VOCs had positive benefits, particularly for controlling alkenes. Despite ongoing reductions in anthropogenic VOCs, the elevated temperatures led to an increase in natural VOCs emissions. On average, a 1°C temperature decrease could reduce the reactivity ratio of VOCs to NOx (VOCR/NOxR) by 0.12, thereby enhancing the advantages of emission reductions. Therefore, implementing measures to alleviate extreme heatwaves, such as limiting high-energy consumption and inducing artificial rainfall, can simultaneously reduce the intensity and reactivity of VOC emissions, aiding in the effective implementation of ozone pollution control policies.

Characteristics and Sources of Volatile Organic Compounds （VOCs） in Luohe City During Summer

Luohe City is an important node city in the Central Plains Urban Agglomeration in China, where the atmospheric ozone （O3） pollution situation has been serious in recent years. In order to provide a scientific basis for O3 pollution control, the online filed observation of O3 precursor volatile organic compounds （VOCs） was carried out in Luohe City in July 2022 to understand their variation characteristics and sources. The mean ratio of φ（TVOCs） during the observation period was （16.49±5.73）×10-9. Among them, alkane （33.7%）, oxygenated volatile organic compounds OVOC （24.0%）, and halohydrocarbon （21.9%） accounted for the top three. The results from source apportionment showed that the main VOCs sources （contributions） included the natural gas （NG） use （20.1%）, regional transport （14.8%）, solvent use （14.2%）, gasoline vehicle emissions （12.3%）, industrial emissions （11.6%）, diesel vehicle emissions （10.5%）, liquefied petroleum gas （LPG） use （9.8%）, and plant emissions （6.7%）. OVOC contributed the most to ozone formation potential （OFP） and free radical loss rate （L·OH）. The results showed that the contribution of motor vehicle exhaust （>22.8%） was the primary source of VOCs in Luohe City. However, other sources were complex and with comparable contributions, requiring the development of targeted and comprehensive prevention and control measures.

Significant Biogenic Source of Oxygenated Volatile Organic Compounds and the Impacts on Photochemistry at a Regional Background Site in South China.

Oxygenated volatile organic compounds (OVOCs) significantly modulate atmospheric chemistry, but the sources and air quality impacts of OVOCs in aged urban outflows remain to be elucidated. At a background site in South China, the ozone formation potential of six nonformaldehyde OVOCs studied was equivalent to that of 3.56 ppbv of formaldehyde, more than half of which was contributed by acetaldehyde. Source apportionment incorporating photochemical age revealed that considerable fractions (52.7%-62.6%) of the OVOCs were of biogenic origin, except for ethanol, which was primarily derived from anthropogenic emissions. The oxidation of cis-/trans-2-butene explained 71.1% of the in situ acetaldehyde formation. In contrast, α/β-pinenes and isoprene contributed 73.8% and 28.4% to acetone and methylglyoxal formation, respectively. An average of 12.4% of net in situ ozone (O3) production rate was attributed to the OVOCs studied, where the biogenic fractions accounted for 59%. The changes in the O3 production rate and hydroxyl radical (OH) concentration caused by OVOCs were mainly affected by ozone formation sensitivity. The effects of primary acetaldehyde and acetaldehyde-led O3 on secondary acetaldehyde formation were weak at this background site; however, they cannot be ignored in polluted areas. This study provides a scientific basis for mitigating O3 pollution driven by biogenic emissions and OVOCs.

Carbonyl Compounds Observed at a Suburban Site during an Unusual Wintertime Ozone Pollution Event in Guangzhou

Carbonyl compounds are important oxygenated volatile organic compounds (VOCs) that play significant roles in the formation of ozone (O3) and atmospheric chemistry. This study presents comprehensive field observations of carbonyl compounds during an unusual wintertime ozone pollution event at a suburban site in Guangzhou, South China, from 19 to 28 December 2020. The aim was to investigate the characteristics and sources of carbonyls, as well as their contributions to O3 formation. Formaldehyde, acetone, and acetaldehyde were the most abundant carbonyls detected, with average concentrations of 7.11 ± 1.80, 5.21 ± 1.13, and 3.00 ± 0.94 ppbv, respectively, on pollution days, significantly higher than those of 2.57 ± 1.12, 2.73 ± 0.88, and 1.10 ± 0.48 ppbv, respectively, on nonpollution days. The Frame for 0-D Atmospheric Modeling (F0AM) box model simulations revealed that local production accounted for 62–88% of observed O3 concentrations during the pollution days. The calculated ozone formation potentials (OFPs) for various precursors (carbonyls and VOCs) indicated that carbonyl compounds contributed 32.87% of the total OFPs on nonpollution days and 36.71% on pollution days, respectively. Formaldehyde, acetaldehyde, and methylglyoxal were identified as the most reactive carbonyls, and formaldehyde ranked top in OFPs, and it alone contributed 15.92% of total OFPs on nonpollution days and 18.10% of total OFPs on pollution days, respectively. The calculation of relative incremental reactivity (RIR) indicates that ozone sensitivity was a VOC-limited regime, and carbonyls showed greater RIRs than other groups of VOCs. The model simulation showed that secondary formation has a significant impact on formaldehyde production, which is primarily controlled by alkenes and biogenic VOCs. The characteristic ratios and backward trajectory analysis also indicated the indispensable impacts of local primary sources (like industrial emissions and vehicle emissions) and regional sources (like biomass burning) through transportation. This study highlights the important roles of carbonyls, particularly formaldehyde, in forming ozone pollution in megacities like the Pearl River Delta region.

Source Profiles of VOCs for Different Types of Industrial Boilers in Sichuan, China

Seven different types of industrial boilers in Sichuan Province were selected to determine the VOC emission components and the source profiles of VOCs containing 115 components were established using Teflon sampling and GC-MS/FID analysis. The ozone formation potential （OFP） and emission factors of VOCs from different types of industrial boilers were analyzed. The results showed that the VOC components emitted from different types of industrial boilers were different. Oxygenated volatile organic compounds （OVOCs） and halogenated hydrocarbons were the major components of biomass boilers, with a total contribution rate of more than 60%. The primary VOC emission species included dichloromethane, ethylene, acetone, acetaldehyde, acetylene, and toluene. Halogenated hydrocarbons （50.7%） were the chief emission components of coal-fired boilers, followed by aromatic hydrocarbons and OVOCs. Dichloromethane, ethylene, acetaldehyde, ethyl acetate, and benzene hydrocarbon were the major VOC emission species. The emission of alkanes （59.7%） in natural gas boilers was prominent, particularly ethane and isopentane. The OFP values of VOC emissions from coal-fired, biomass, and natural gas industrial boilers were 6.1, 28.7, and 4.7 mg·m-3, respectively. Alkenes were the primary OFP contributors （35.1%-59.5%） in different types of industrial boilers. OVOCs （32.8%） in biomass boilers and aromatic hydrocarbons （43.0%） in coal-fired boilers also contributed significantly to OFP. The VOC emission factors of coal-fired, biomass, and natural gas industrial boilers in Sichuan Province were （17.3 ± 10.7） g·t-1, （90.6 ± 42.1） g·t-1, and 0.10 g·m-3, respectively. The VOC emission level of biomass boilers was higher than that of coal-fired boilers and VOC emission control could not be ignored.

Pollution Characteristics and Source Apportionment of Volatile Organic Compounds in Typical Solvent-using Industrial Parks in Beijing

The BCT-7800A PLUS VOC online monitor system was employed to measure ambient volatile organic compounds （VOCs） in a typical solvent-using industrial park in Beijing. From January to June 2023, the pollution characteristics, source apportionment, and ozone formation potential（OFP）of VOCs were studied, and the results of a comparative analysis were also discussed between heating and non-heating periods. The results indicated that VOC concentrations from January to June 2023 were （104.21 ± 91.31） μg·m-3 on average. The concentrations of TVOCs under the influence of southerly and northerly winds were （214.18 ± 202.37） μg·m-3 and （197.56 ± 188.3） μg·m-3, respectively. Alkanes were the species with the highest average concentration and proportion, respectively （45.53 ± 41.43） μg·m-3. The VOC concentration during the heating period was higher than those during the non-heating period, with values of （111.57 ± 83.96） μg·m-3 and （87.92 ± 75.03） μg·m-3, respectively. Propane and ethane were the species with the highest average concentration during the heating period. Compared with those in the non-heating period, the average concentrations of three species （propane, ethane, and n-butane） in the top ten species increased during the heating period, with average concentrations increasing by 51.94%, 54.64%, and 26.32%, respectively. The source apportionment results based on the positive matrix factorization （PMF） model indicated that the major sources of VOCs in the park during the monitoring period were printing emission sources （4.95%）, oil and gas evaporation sources （9.52%）, fuel combustion sources （15.44%）, traffic emissions sources （18.97%）, electronic equipment manufacturing （24.59%）, and industrial painting sources （26.52%）. Therefore, industrial painting sources, electronic equipment manufacturing sources, and traffic emissions sources were the emission sources that the park should focus on controlling. Compared with those during non-heating periods； industrial painting, traffic emission, and fuel combustion sources contributed more during the heating period, with VOC concentrations increasing by 15.02%, 16.53%, and 24.98%, respectively. The average OFP of VOCs from May to June during the monitoring period was 198.51 μg·m-3 and OVOCs, olefins, and aromatic hydrocarbons contributed the most to OFP, which were 47.41%, 22.15%, and 18.41%, respectively. The electronic equipment manufacturing source was the largest contributor to the summer OFP of the park and its contribution rate was 30.11%, which should be strengthened in the future.

Analysis of Ozone Pollution and Precursor Control Strategies in the Pearl River Delta During Summer and Autumn Transition Season

To analyze the causes of ozone pollution in the Pearl River Delta （PRD） Region during the summer and autumn transition seasons, a case study was carried out in Guangzhou, which is located in the center of the PRD Region, to analyze the ozone photochemical production and destruction pathways as well as emission reduction scenarios using a box model based on comprehensive observation. The results showed that the stagnant meteorological conditions and high temperature during the observation period were suitable for the photochemical production of ozone, which led to widespread and prolonged ozone pollution. Aromatic hydrocarbons （AHs） contributed the most to the ozone formation potential （OFP）, and m/p-xylene, toluene, and o-xylene were the major three VOC species contributing to the OFP. Box model analysis revealed that the averaged net O3 production rate during the polluted period was 23.2×10-9 h-1 and the peak reached 39.2×10-9 h-1. The HO2·+NO and NO2+·OH reaction pathways contributed the most to the local photochemical ozone production （51.2%） and destruction （47.0%）, respectively. Observed ozone concentration was primarily controlled by both the local photochemical O3 production and the export-dominated transport. The RIR and EKMA analyses showed that O3 formation in Guangzhou during the summer-autumn transition seasons was mainly a VOC-limited regime and AHs showed the greatest sensitivity to O3 production. Toluene, m/p-xylene, o-xylene, n-butane, and propylene were the five key components affecting O3 generation. The analysis of reduction scenarios showed that reducing anthropogenic VOC emissions was the most favorable way to reduce O3 concentrations； however, if NOx emission was controlled after reducing VOCs, the O3 concentration would rebound in a short time. Our results suggested that the synergistic reduction of VOCs and NOx while mainly focusing on VOCs alleviation should be implemented to continuously reduce ozone concentrations in the future.

Spatial heterogeneity of volatile organic compound pollution in a typical industrial park based on multi-point online monitoring: Pollution characteristics, health risks, and priority-controlled species

Emissions from industrial parks are crucial sources of ambient volatile organic compound (VOC) pollution, characterized by high concentrations, complex compositions, dispersed emission sources, and uneven spatial distribution. To better understand and address this issue, it is crucial to analyze the spatial differences in VOC pollution and associated health risks through multi-point monitoring. In this study, we established four online monitoring sites in a typical industrial park in Kaifeng, China. We monitored 115 VOC species and found significant differences in the concentration and chemical composition of total VOCs (TVOCs) among the four sites. Two sites were primarily composed of halohydrocarbons (49.80% and 41.21%), while the other two sites had a higher proportion of aromatics (54.78% and 39.03%). Acetaldehyde was the main contributor to ozone formation potential (OFP) at one site, while toluene was associated with the other three sites. The site with the highest VOC concentration and OFP also showed the highest secondary organic aerosol formation potential (SOAP). In terms of health risk assessment, acrolein posed a non-carcinogenic risk at all sites, but there were disparities in the carcinogenic risk among the four sites. 1,2-Dichloroethane at one site exceeded the definite risk limit, while 1,2-dibromoethane and chloroform were considered probable risk species at another site. Considering both the environmental impact and health risk, we used entropy-weighting to calculate a comprehensive control index (CCI). This index identified 1,2-dichloroethane as the Level Ⅰ controlled pollutant species at two sites, and toluene at the other two sites. This study highlights the spatial heterogeneity in VOC pollution and health risks within the industrial park, providing valuable insights for targeted pollution control strategies.

Characterization and source apportionment of ambient VOC concentrations: Assessing ozone formation potential in the Barnett shale oil and gas region

Atmospheric concentration and distribution of volatile organic compounds (VOC) are influenced by localized emissions and the fate and transport of secondary products formed through photochemical reactions. This study identifies the sources of VOC and its contribution to ozone formation in the Barnett Shale region, specifically in Denton, Texas, during the ozone seasons of 2015 through 2022. A total of 31 critical ozone precursor VOC compounds were observed at this site with an average total VOC concentration of 146 ppb-C, with n-alkanes from extensive oil and gas activities in the area contributing to 96.64% of the total VOC. Source apportionment using dispersion normalized positive matrix factorization (DN-PMF) identified eight VOC sources, with natural gas emissions (72%) being the dominant source followed by a combined source of natural gas combustion and aviation emissions (8.3%). Ozone formation potential (OFP) by VOC species was calculated using the propylene-equivalent concentration (propy-equiv) method. OFP calculated for all the apportioned sources highlighted that natural gas sources contributed significantly to the ozone formation in this region besides isoprene from biogenic sources and reactive alkenes from urban and industrial activities. This study underscores the critical role of slow-reacting n-alkanes along with other highly reactive VOC from urban and industrial sources influencing ambient air quality and it identifies strategies for mitigating ground-level ozone in urban areas affected by oil and gas extraction and production.

Atmospheric Degradation Mechanism of Isoamyl Acetate Initiated by OH Radicals and Cl Atoms Revealed by Quantum Chemical Calculations and Kinetic Modeling.

Isoamyl acetate is one of the volatile organic compound class molecules relevant to agricultural and industrial applications. With the growing interest in isoamyl acetate applications in industry, the atmospheric fate of isoamyl acetate must be considered. Reaction mechanisms, potential energy profiles, and rate constants of isoamyl acetate reaction with atmospheric relevant oxidant OH radicals and Cl atoms have been obtained from the quantum chemical calculations and kinetic modeling. The geometry optimizations were conducted using M06-2X/6-311++G(3df,3pd) followed by single point-energy calculations at the DLPNO-CCSD(T) method with an extrapolated complete basis set. The rate constants were calculated by solving the master equation. A hydrogen-abstraction reaction dominates the first step of isoamyl acetate degradation, while the addition-substitution reaction plays a small role in the degradation products. The kinetic study was conducted to evaluate the rate constants within a temperature range of 200-400 K. The total rate constants for the isoamyl acetate degradation reactions initiated by the OH radical and Cl atom were determined to be 6.96 × 10-12 and 1.27 × 10-10 cm3 molecule-1 s-1, respectively, under standard temperature and pressure conditions. The product degradation mechanism, ozone formation potential, and atmospheric impacts were discussed.

A comprehensive evaluation of the atmospheric impacts and health risks of cooking fumes from different cuisines

Pollutants emitted by catering enterprises pose a significant threat to the environment and public health. In this study, based on a systematic analysis of volatile organic compound (VOC) emission characteristics of different cuisines, the contribution of cooking emissions from catering enterprises to the PM2.5 and O3 concentrations in the atmosphere was evaluated using generation potential calculations and WRF-CAMx simulations. The health exposure risks of VOCs in kitchen breathing areas and those of PM2.5 and O3 contributed by the catering enterprises were evaluated. The generation potential calculation results showed that the catering enterprises exhibit 2.21–5.00 gO3/gVOCs of ozone formation potential (OFP) and 0.07–0.21 gSOA/gVOCs of secondary organic aerosol production potential (SOAP). The WRF-CAMx simulation results indicated that cooking emissions from catering enterprises contribute 0.36–1.91 μg/m3 and 0.05–0.21 μg/m3 to PM2.5 and maximum daily 8-h average (MDA8) concentrations of O3. The health exposure risks of PM2.5 and O3 were higher in catering enterprises in southern cities than in northern cities and were higher in urban areas than in suburban areas. The average hazardous VOCs (HVOCs) concentrations ranged from 53 ± 16 to 357 ± 31 μg/m3 in kitchen breathing areas. Acrolein was the primary contributor to the hazard index (HI) of all VOC species, accounting for 50.9%–99.5%. The total incremental lifetime carcinogenic risk (ILCR) of all cuisines exceeded the acceptable thresholds of 1.00 × 10−6. These findings provide insights that can aid in the formation and implementation of pollutant mitigation strategies in the catering industry.

First exploratory study of gaseous pollutants (NO2, SO2, O3, VOCs and carbonyls) in the Luanda metropolitan area by passive monitoring

An air quality monitoring campaign for gaseous pollutants using passive sampling techniques was carried out, for the first time, at 25 locations in the metropolitan area of Luanda, Angola, in June 2023. Concentrations of benzene, toluene, ethylbenzene, xylenes, trimethylbenzenes, SO2 and NO2 were generally higher in locations more impacted by traffic. Benzene, SO2 and NO2 levels did not exceed the World Health Organisation guidelines. Ozone concentrations surpassed those documented for other African regions. Higher O3 formation potential values were recorded at heavy-trafficked roads. The top 5 species with potential for ozone formation were m,p-xylene, toluene, formaldehyde, propionaldehyde and butyraldehyde. The Mulenvos landfill presented a distinctive behaviour with a very low toluene/benzene ratio (0.47), while values close to 5 were obtained at traffic sites. The maximum levels of α-pinene, D-limonene, formaldehyde, acetaldehyde, acetone, acrolein, propionaldehyde, butyraldehyde, benzaldehyde, valeraldehyde, hexaldehyde and crotonaldehyde were recorded at the landfill. The formaldehyde/acetaldehyde ratio ranged from 0.40 at the Mulenvos landfill to 3.0, averaging 1.8, which is a typical value for urban atmospheres. Acetaldehyde/propionaldehyde ratios around 0.4–0.6 were found in locations heavily impacted by traffic, whereas values between 0.7 and 1.2 were observed in green residential areas and in places with more rural characteristics. All hazard quotient (HQ) values were in the range from 1 to 10, indicating moderate risk of developing non-cancer diseases. The exception was the Mulenvos landfill for which a HQ of 11 was obtained (high risk). The cancer risks exceeded the tolerable level of 1 × 10−4, with special concern for the landfill and sites most impacted by traffic. A mean lifetime cancer risk of 9 × 10−4 was obtained. The cancer risk was mainly due to naphthalene, which accounted, on average, for 94.6% of the total.

Ambient volatile organic compounds in a typical industrial city in southern China: Impacts of aromatic hydrocarbons from new industry

New industrial parks, including fine chemical, medical manufacturers, etc., are emerging in modern cities in China, whereas their emissions and impacts have not been fully illuminated. In this study, ambient volatile organic compounds (VOCs) in Huizhou were measured in three functional zones, namely new industrial, roadside, and residential zones. The average mixing ratios of total VOCs were as follow: industrial (56.22 ± 15.06 ppbv) > roadside (39.30 ± 12.96 ppbv) > residential (26.03 ± 7.31 ppbv). The ozone formation potential (OFP) and secondary organic aerosol formation potential (SOAP) of VOCs in the industrial zone were 1.5–2.3 and 1.7–3.1 times those in the other zones, respectively. Aromatics contributed the most to OFP (39.8 % - 44.8 %) and SOAP (78.9 % - 91.0 %), with much less contributions to VOCs mixing ratios (18.3 % - 21.2 %). Naphthalene was the most abundant aromatic species across the three zones and ranked among the top contributors to OFP and SOAP among all VOCs species. Source apportionment identified that new industrial emissions and solvent use was the largest VOCs contributor in the industrial zone (53.9 %), traffic-related emissions dominated in the roadside zone (40.7 %), while new industrial and traffic-related emissions contributed similar in the residential zone (32.9 % and 34.7 %, respectively). The carcinogenic and non-carcinogenic risks of hazardous VOCs were above the acceptable threshold, primarily due to new industrial and traffic-related emissions. Our results suggested to strengthen the control of new industrial emissions and aromatics sources in Huizhou city to improve air quality and protect human health.

Biomass-burning sources control ambient particulate matter, but traffic and industrial sources control volatile organic compound (VOC) emissions and secondary-pollutant formation during extreme pollution events in Delhi

Abstract. Volatile organic compounds (VOCs) and particulate matter (PM) are major constituents of smog. Delhi experiences severe smog during the post-monsoon season, but a quantitative understanding of VOCs and PM sources is still lacking. Here, we conduct a source apportionment study for VOCs and PM using a recent (2022), high-quality dataset of 111 VOCs, PM2.5, and PM10 in a positive matrix factorization (PMF) model. Contrasts between clean monsoon air and polluted post-monsoon air, VOC source fingerprints, and molecular tracers enabled us to differentiate paddy residue burning from other biomass-burning sources, which had previously been impossible. Burning of fresh paddy residue, as well as residential heating and waste burning, contributed the most to observed PM10 levels (25 % and 23 %, respectively) and PM2.5 levels (23 % and 24 %, respectively), followed by heavy-duty vehicles fuelled by compressed natural gas (CNG), with a PM10 contribution of 15 % and a PM2.5 contribution of 11 %. For ambient VOCs, ozone formation potential, and secondary-organic-aerosol (SOA) formation potential, the top sources were petrol four-wheelers (20 %, 25 %, and 30 %, respectively), petrol two-wheelers (14 %, 12 %, and 20 %, respectively), industrial emissions (12 %, 14 %, and 15 %, respectively), solid-fuel-based cooking (10 %, 10 %, and 8 %, respectively), and road construction (8 %, 6 %, and 9 %, respectively). Emission inventories tended to overestimate residential biofuel emissions at least by a factor of 2 relative to the PMF output. The major source of PM pollution was regional biomass burning, while traffic and industries governed VOC emissions and secondary-pollutant formation. Our novel source apportionment method even quantitatively resolved similar biomass and fossil fuel sources, offering insights into both VOC and PM sources affecting extreme pollution events. This approach represents a notable advancement compared to current source apportionment approaches, and it could be of great relevance for future studies in other polluted cities and regions of the world with complex source mixtures.

Volatile organic compounds in typical coal chemical industrial park in China and their environmental and health impacts

The coal chemical industry produces a large amount of volatile organic compounds (VOCs), and the emission characteristics and associated impact on the environment and health of the residents are still unclear. This study determined the VOC concentrations and compositions in the Jinjie Coal Chemical Industry Park which is located in northern China. The average concentrations of total measured VOCs (TVOCs) in the industrial areas in summer and winter were 231.5 and 103.2 μg/m3, which were higher than those in the residential areas (123.7 and 70.3 μg/m3), respectively. Aromatics, Oxygenated volatile organic compounds (OVOCs), and alkanes were the dominant VOC classes in the industrial areas, while halocarbons, OVOCs, and alkenes had higher compositions in the residential areas where were not only affected by industrial emissions and also other anthropogenic sources. OVOCs contributed over 43% of ozone formation potential (OFP), while aromatics contributed over 61% of secondary organic aerosol (SOA) formation in the Park in both seasons. Using the source apportionment method, biogenic emission and anthropogenic source (gasoline production, coking emission, fuel combustion, solvent coating, and vehicle exhaust) were major contributors to VOCs in residential areas. The industrial-related emissions were the main components of anthropogenic source, accounting for 53.5%–58.7% of the overall VOCs. With reliable estimations of the health aspects, exposures to acrolein (HQ: 7.4–126.6) and formaldehyde (ILCR: 5.5 × 10−3-5.7 × 10−2) posed the highest non-carcinogenic and carcinogenic risks, accounting for 94.3%–98.6% and 55.8%–93.8% of the total HQ and ILCR, respectively. The results demonstrated that substantial environmental and health co-benefits to the residents could be achieved by reducing the industrial emissions from gasoline production, coking process, and diesel-fueled vehicles in the Jinjie Coal Chemical Industry Park. Prioritizing the establishment of efficient air pollution measures and tightening industrial emission standards, especially for hazardous VOCs, are recommended according to the findings of the valuable work.