Ambient Volatile Organic Compounds Research Articles

Analysis of Ozone and VOCs Pollution Characteristics, Sources, and Abatement Control Strategies in Hebi

In order to control the increasing ozone （O3） pollution in Hebi, Henan Province, clarifying the pollution characteristics of ozone and its precursors is vital. Therefore, we conducted a comprehensive analysis of O3 pollution utilizing the OFP-PMF-EKMA method combined with online hourly resolution monitoring data of conventional pollutants and volatile organic compounds （VOCs） in the summer of 2022 （June-September）. Ozone formation potential （OFP） was used to identify the key VOCs species, and the PMF model was used to identify the VOCs emission sources, whereas EKMA curves and scenario analysis were used to identify the main ozone control area in Hebi and to determine the reduction ratio of VOCs and NOx in a scientifically refined way. In 2022, Hebi had persistent O3 pollution, with the highest concentration in June. Conditions of high temperature, low humidity, and low atmospheric pressure contributed to the O3 accumulation. Aromatic and oxygenated volatile organic compounds （OVOCs） contributed significantly to the OFP and VOCs fraction, which were the dominant active substance and concentration dominant species. The results of the VOCs source analysis indicated that vehicle exhaust sources （25.3%） were the main source of atmospheric VOCs, followed by process sources （17.7%） and biomass combustion sources （17.6%）. Thus, emission sources associated with the combustion of fossil fuels and industrial production emissions were the most urgent sources of atmospheric VOCs to be controlled in Hebi. The O3 generation in Hebi occurred in the VOCs-sensitive zones, and the emission reduction results showed that a synergistic emission reduction of VOCs and nitrogen oxide （NOx） could effectively control O3 pollution with a 75% reduction in VOCs and a 10% reduction in NOx.

The impacts of photochemical loss on the source apportionment of ambient volatile organic compounds: A case study in Northern China

Volatile organic compounds (VOCs) play a crucial role as precursors in the formation of ozone (O3) and secondary PM2.5. It is well-established that some VOC species exhibit high photochemical reactivity, leading to deviations between measured and initial concentrations. Therefore, precise source apportionment must consider these photochemical reaction which called photochemical losses. The study was conducted in Langfang, which located in an important site for pollution transferring to Beijing, with August to October as the sampling period. The initial concentrations of the VOC species were estimated using a photochemical age-based parameterization method. The effects of photochemical losses on source apportionment were compared by the positive matrix factorization (PMF) results, based on observed and initial concentration data. The results showed that neglecting photochemical losses would result in an underestimation of VOCs concentration by 6.7% compared to the measured values obtained in this study. Furthermore, olefins and aromatic hydrocarbons were found to be the key components involved in photochemical reactions, with a photochemical loss rate of 28.3% and 23.7%, respectively. VOCs source apportionment revealed that the impact of photochemical loss on source apportionment was significant. Results indicated that biogenic sources (−6.8%) and solvent usage (−5.9%) made a higher contribution based on initial VOCs compared to measured VOCs, while gasoline vehicular emissions showed a lower contribution (+7.9%) than that observed from measured VOCs data. Analysis results also demonstrated that the combustion sources accounted for 14.2% based on measured concentrations and that accounted for 9.5% based on initial concentrations.

Effects of VOC emission reduction on atmospheric photochemistry and ozone concentrations during high-ozone episodes

We studied atmospheric volatile organic compounds (VOCs) characteristics and sources during fifteen high ozone (O3) episodes (daily 1-h maximum >100 ppbv and maximum 8-h average > 80 ppbv) in Nanjing, China, and used a photochemical box model to study the O3 formation sensitivity of VOCs, O3 photochemistry, radical budget, and reactivity for different emission reduction scenarios together with the base case ones. Overall, emission reduction from biogenic sources, followed by combustion sources, multiple sources, and solvent usage, had the major impacts on the O3 concentrations. According to photochemical box model simulations, isoprene was the most sensitive or influential VOC in the formation of O3, followed by ethylene, o-xylene, and cis-2-pentene. A 20.6 ± 11.7% concentration reduction of the sixteen most sensitive VOCs (SV16) for the production of O3 could bring the O3 concentration below the national standard level (daily 1-h maximum <100 ppbv). Besides, a 30% emission reduction from all the anthropogenic sources was more than enough to bring the O3 concentration below the national standard level. The total emission reduction of alkenes was always enough to bring the O3 concentration below the national standard level, which was not the case for aromatics under severe pollution conditions. The simulated OH reactivity analysis illustrates the importance of alkenes and aromatics, which account for about half of the total OH reactivity. The highest OH reactivity decreased due to the emission reduction for biogenic sources, followed by combustion and multiple sources. Alkenes played a major role in the OH, HO2, and RO2 radical's formation in the study area. The biggest drop in OH, HO2, and RO2 radical concentrations was noticed for biogenic emission reduction, followed by combustion and multiple sources. Due to the emission reduction from VOC sources, the highest O3 formation rates decreased for biogenic sources, followed by combustion and multiple sources. The acquired information is valuable to the scientific community and policymakers for formulating and implementing O3 pollution control strategies.

Anthropogenic-driven changes in concentrations and sources of winter volatile organic compounds in an urban environment in the Yangtze River Delta of China between 2013 and 2021

Volatile organic compounds (VOCs) serve as crucial precursors to surface ozone and secondary organic aerosols (SOA). In response to severe air pollution challenges, China has implemented key air quality control policies from 2013 to 2021. Despite these efforts, a comprehensive understanding of the chemical composition and sources of urban atmospheric VOCs and their responses to emission reduction measures remains limited. Our study focuses on analyzing VOCs composition and concentrations during the winters of 2013 and 2021 through online field observations in urban Nanjing, a typical city in the Yangtze River Delta region of China. Using a machine learning approach, we found a notable reduction in total VOCs concentration from 52.4 ± 30.4 ppb to 33.9 ± 21.6 ppb between the two years, with dominant contributions (approximately 94.3 %) associated with anthropogenic emission control. Furthermore, alkanes emerged as the major contributors (48.6 %) to such anthropogenic-driven decline. The total SOA formation potential decreased by approximately 27.4 %, with aromatics identified as the major contributing species. Positive matrix factorization analysis identified six sources. In 2013, prominent contributors were solid fuel combustion (43.6 %), vehicle emission (16.7 %), and paint and solvent use (12.8 %). By 2021, major sources shifted to solid fuel combustion (31.9 %), liquefied petroleum gas and natural gas (26.8 %), and vehicle emission (25.5 %). Solid fuel combustion emerged as the primary driver for total VOCs reduction. The lifetime carcinogenic risk in 2021 decreased by 72.6 % relative to 2013, emphasizing the need to address liquefied petroleum gas and natural gas source, and vehicle emissions for improved human health. Our findings contribute critical insights for policymakers working on effective air quality management.

Development of a UAV-borne sorbent tube sampler and its application on the vertical profile measurement of volatile organic compounds

Vertical detection of volatile organic compounds (VOCs) is essential to expend our understanding of the distribution characteristics of VOCs and improve the predictive ability of existing air quality models. In this work, we report the development of a sorbent tube sampler based on an unmanned aerial vehicle (UAV) platform. Vertical profile measurement of VOCs with a vertical resolution of 25 m was achieved. The sampler consists of five lightweight VOC sorbent tubes and a 5-way solenoid valve, making it available for collecting five atmospheric VOC samples in a single flight with a time response of less than 30 min. The sampler weighed ∼ 1.45 kg and had dimensions of 240 mm × 220 mm × 100 mm with small penetration loss (< 10%) under 4-liter sampling conditions (flow rate of 200 mL/min). Commercialized SUMMA canisters were used as experimental controls to investigate the possible loss of self-made sampler for target compounds in the same sampling process. Comparison experiment on the ground showed that the concentration differences for all VOC species were lower than 0.14 μg/m3, proving the good reliability for VOCs measurements using sorbent tube sampler. The UAV platform also incorporated online instruments for meteorological parameters and O3 measurement. The sampler was successfully applied to characterize the vertical profiles of VOCs up to 100 m in October 2023 in the Huaihe River Basin of China. The UAV platform and the sorbent tube sampler demonstrate good performance and will be a valuable and reliable tool for vertical VOCs measurement.

Characteristic, source apportionment and effect of photochemical loss of ambient VOCs in an emerging megacity of Central China

During the transportation from emission sources to sampling site, volatile organic compounds (VOCs) undergo photochemical losses which have significant effects for tropospheric ozone (O3) formation and VOCs source apportionment. In this study, based on hourly speciated VOC data from May 23, to July 8, 2019 with high O3 concentrations, the concentration level, chemical composition, and diurnal variation of observed VOCs were studied, and the initial concentration of VOCs was obtained by combining the local emission inventory in Zhengzhou, Central China. The impact of photochemical loss on source apportionment was evaluated using the Positive Matrix Factorization/Multilinear Engine 2-Species Ratio (PMF/ME2-SR) model based on observed and initial VOCs concentration (OC-PMF and IC-PMF). Results suggest that during the observed period, the average concentration of total VOCs (TVOCs) was 23.74 ± 9.20 ppbv, and alkanes (3.92 ± 2.40 ppbv) were the predominant component. The photochemical losses of TVOCs were approximately 10.15 ± 7.13 ppbv, with an average loss rate of 29.9%. The ozone formation potential (OFP) based on the initial VOCs concentration was 2.2 times higher than that observed VOCs concentration. Alkenes contributed the most to OFP and were also the largest contributors to photochemical losses. TVOC concentrations increased by 5.0% during O3 pollution compared to non-O3 pollution. Seven sources of VOCs were determined, including biomass burning, liquefied petroleum gas (LPG), vehicle emission, industrial emission, solvent usage, gasoline evaporation, and biogenic emission. Compared to the results of IC-PMF, the contributions of these sources in OC-PMF were underestimated by 15.4%, 14.4%, 13.0%, 11.7%, 31.5%, 7.6%, and 4.7%, respectively. This study still exhibits certain limitations in calculation method, and further exploration can be conducted in the future.

Health Risk Assessment from Exposure to Ambient Volatile Organic Compounds (VOCs) at a Truck Tire Factory in the Yangtze River Delta, China

Occupational health risk assessments of exposure to VOCs still need to be extensively studied to improve the safety standards in the industry. Based on the monitoring of organic pollutants at various workstations in a truck tire factory in Jiangsu Province, both semi-quantitative and quantitative health risk assessment methods were employed to assess health risk levels. The findings indicated that VOCs were categorized into five classes, which included alkanes, aromatics, halocarbons, carbon disulfide, and oxygenated volatile organic compounds (OVOCs). The highest concentration of total volatile organic compounds (TVOCs) was found in shaping workshop; alkanes were the most abundant class (74.2%), followed by aromatics (24.02%) and OVOCs (1.96%). Although the results of the semi-quantitative risk assessment showed that most of the organic compounds had low R values, various kinds of VOCs were detected; particularly, many harmful organic compounds (such as toluene, ethyl benzene) were detected in all the sampling sites. The quantitative risk in the calendering and vulcanizing workshop exceeded the acceptable level; both the carcinogenic risk of ethylbenzene in the tire-strip storage room, and trichloroethylene and perchloroethylene in the calendering workshop were unacceptable. Thus, the calendering and vulcanizing processes in rubber tire manufacturing should be priority-controlled processes.

Multi-generation oxidation mechanism of M-xylene: Unexpected implications for secondary organic aerosol formation

Secondary organic aerosol (SOA) affects air quality, human health and climate. The multi-generation reactions of volatile organic compounds (VOCs) have become key process for explaining the SOA formation. M-xylene, as one of the most important VOCs in urban atmosphere, has got extensive study. However, the reaction mechanism of the first-generation products hydroperoxides (M-ROOH) and organonitrates (M-RONO2) remain unknown. In this work, the hydroxyl radicals (·OH) initiated reactions of M-ROOH and M-RONO2 were investigated by employing quantum chemical methods and kinetics modeling. The results show that new ring-retaining epoxides, a range of dialdehydes and less volatile hydroperoxides and organonitrates are formed, contributing to SOA formation. By adopting the unveiled new mechanism into the SOSAA box modeling, we found that the yield of SOA from m-xylene oxidation is up to 38%, which is comparable to the experimental value (36%). This work advances current understanding of multi-generation chemistry and elucidates the role of aromatic hydrocarbons oxidation in the formation of SOA.

Anti-competitive adsorption of gaseous benzene on hydrophilic microporous carbon in humid conditions

The adsorption capture of ambient volatile organic compounds (VOCs) is of practical importance for air quality management. Herein, unique anti-competitive adsorption behavior of benzene on a hydrophilic activated carbon (Procarb-900 (P900)) is evidenced in the presence of competing components (e.g., formaldehyde (FA) and/or moisture). Contrary to general expectations, the adsorption capacity of 10 Pa benzene (QB) onto P900 (30 mg) at the 99 % breakthrough level improves from 144.8 to 187 mg g−1 as the relative humidity (RH) increases from 0 to 25 %. Such pattern is maintained at 183.9 mg g−1 even at the relatively high RH of 50 %. Furthermore, QB exhibits a remarkable increase of 56.1 % (to 226.0 mg g−1) in the binary phase (100 ppm benzene plus 50 ppm FA) relative to its single phase (144.8 mg g−1). The kinetic studies confirm the occurrence of anti-competitive adsorption of benzene under humid conditions with the unusual decrease in rate constants at the elevated RHs (i.e., 25 and 50 %). The thermodynamic studies suggest the exothermic nature of benzene adsorption onto P900. The hydrophilicity of P900's outer surface promotes the preferential adsorption of polar FA and water vapor over non-polar benzene, which deforms the activated carbon texture and lowers the pore size distribution (PSD). The narrow PSD enhances benzene uptake in the complex systems due to the confinement effect. Overall, this study offers insights into the unique anti-competitive adsorption of non-polar VOCs (e.g., benzene) on hydrophilic microporous adsorbents in the presence of potential interferences such as polar water vapor and FA. These findings offer a guideline for the practical implementation of adsorption techniques for gaseous VOCs in humid conditions.

Ambient volatile organic compounds in the Seoul metropolitan area of South Korea: Chemical reactivity, risks and source apportionment

The chemical reactivity, contribution of emission sources, and risk assessment of volatile organic compounds (VOCs) in the atmosphere of the Seoul metropolitan area (SMA) were analyzed. Datasets collected from 6 photochemical assessment monitoring stations (PAMS) of SMA from 2018 to 2021 were used. Alkenes and aromatics contributed significantly to ozone formation relative to the emission concentrations, and aromatics accounted for most of the secondary organic aerosols (SOA) formation in the SMA. The contributions of ozone and SOA formation were found to be notably higher at measurement stations in residential areas such as Guwol (GW) and Sosabon (SS) compared to other measurement stations. From the results of an emission source analysis, it was confirmed that anthropogenic sources such as combustion sources, vehicle exhaust, fuel evaporation, and solvent use had a significant effect at all measurement stations. Assessing the health risk, non-carcinogenic compounds were at acceptable level at all measurement stations. On the other hand, carcinogenic compounds were approaching risk level (10−4), thereby demanding immediate attention. The level of exposure to carcinogenic compounds increased by age group, and male was more vulnerable than female. It was found that SS had the highest level of exposure to carcinogens in the atmosphere of the population ages 60 or older. The health threat of the SMA population is expected due to direct exposure from inhalation of ambient toxic compounds and indirect exposure from ozone and PM2.5 formations through oxidation of VOCs. This study emphasizes the importance of addressing specific emission sources within the metropolitan area and developing comprehensive regional strategies to mitigate VOCs.

Association between Ambient Volatile Organic Compounds Exposome and Emergency Hospital Admissions for Cardiovascular Disease.

The limited research on volatile organic compounds (VOCs) has not taken into account the interactions between constituents. We used the weighted quantile sum (WQS) model and generalized linear model (GLM) to quantify the joint effects of ambient VOCs exposome and identify the substances that play key roles. For a 0 day lag, a quartile increase of WQS index for n-alkanes, iso/anti-alkanes, aromatic, halogenated aromatic hydrocarbons, halogenated saturated chain hydrocarbons, and halogenated unsaturated chain hydrocarbons were associated with 1.09% (95% CI: 0.13, 2.06%), 0.98% (95% CI: 0.22, 1.74%), 0.92% (95% CI: 0.14, 1.69%), 1.03% (95% CI: 0.14, 1.93%), 1.69% (95% CI: 0.48, 2.91%), and 1.85% (95% CI: 0.93, 2.79%) increase in cardiovascular disease (CVD) emergency hospital admissions, respectively. Independent effects of key substances on CVD-related emergency hospital admissions were also reported. In particular, an interquartile range increase in 1,1,1-trichloroethane, methylene chloride, styrene, and methylcyclohexane is associated with a greater risk of CVD-associated emergency hospital admissions [3.30% (95% CI: 1.93, 4.69%), 3.84% (95% CI: 1.21, 6.53%), 5.62% (95% CI: 1.35, 10.06%), 8.68% (95% CI: 3.74, 13.86%), respectively]. We found that even if ambient VOCs are present at a considerably low concentration, they can cause cardiovascular damage. This should prompt governments to establish and improve concentration standards for VOCs and their sources. At the same time, policies should be introduced to limit VOCs emission to protect public health.

Effects of volatile organic compounds and new particle formation on real-time hygroscopicity of PM2.5 particles in Seosan, Republic of Korea

The hygroscopicity of PM2.5 particles plays an important role in PM2.5 haze in Northeast Asian countries by influencing particle growth and chemical composition. New particle formation (NPF) and atmospheric volatile organic compounds (VOCs) are factors that influence particle hygroscopicity. However, the lack of real-time hygroscopicity measurements has deterred the understanding of their effects on particle hygroscopicity. In this study, two intensive monitoring campaigns were conducted during the summer of 2021 and spring of 2022 using real-time aerosol instruments, including a humidified tandem differential mobility analyzer (HTDMA), in Seosan, Republic of Korea. The hygroscopicity parameter κ was calculated from the real-time HTDMA measurement data (κGf). The diurnal variations in κGf exhibited strong inverse linear correlations with the total concentration of VOCs (CTVOC) during the two campaigns. The higher atmospheric CTVOC in summer increased the growth rate of the particle diameter from 10 to 40 nm (6 nm/h) compared with that in spring (2.7 nm/h), resulting in a faster change in κGf for 40-nm particles in summer than in spring because of the increase in organic matter in the chemical compositions of particles. In addition, NPF events introduced additional tiny fresh particles into the atmosphere, which reduced the κGf of 40-nm particles and increased the intensity of the less hygroscopic peaks (κGf < 0.1) of κ-probability density functions (κ-PDF) in NPF days. However, 100-nm particles exhibited fewer changes in κGf than 40-nm particles, resulting in additional dominant hygroscopic peaks (κ ∼ 0.2) of κ-PDFs in both NPF and non-NPF days. When κGf values measured in Seosan were compared with those in other Northeast Asian countries in the literature, the κ values for 40-nm particles were lower than those (κ > 0.2) measured in Beijing and Guangzhou, but those for 100-nm particles were close to those measured in the two cities.

Traceability tagging of volatile organic compound sources and their contributions to ozone formation in Suzhou using vehicle-based portable single-photon ionization mass spectrometry

BackgroundIn recent decades, there has been an increasing global preoccupation with atmospheric volatile organic compounds (VOCs). Given the significant impact of VOCs as pollutants and essential precursors of ozone (O3) in urban and industrial areas, it is imperative to identify and quantify the sources of their emissions to facilitate the development and implementation of effective environmental control strategies.MethodsA mobile laboratory vehicle equipped with a single-photon ionization–time-of-flight mass spectrometer (SPI–TOFMS) and a navigation system was employed to establish the traceability of VOCs that contribute to the formation of ozone in Suzhou Industrial Park. The method exhibited a favorable detection limit of 0.090 ppbv, accompanied by a mass resolution of 1500 for the instrument and a correlation coefficient ≥ 0.990. A positive matrix factorization (PMF) model was utilized to determine the source appointment of the VOCs.ResultsThe study tentatively traced and identified the VOCs emissions source and their contribution to ozone formation in Suzhou. Using the PMF model, the sources of VOCs were profiled: three primary sources of VOCs were identified, namely, vehicular emissions, an industrial solvent, and biofuel combustion. Alkanes groups were found to be the most abundant VOCs species, accounting for 60% of the total VOCs, followed by aromatics and alkenes. Maximum incremental reactivity (MIR) quantifies the impact of photochemical reaction mechanism on the potential ozone formation.ConclusionsThe findings of this study complement existing knowledge on the pollution status of atmospheric VOCs and highlight the correlation with ozone formation potential in Suzhou. The aforementioned sources were identified as the primary factors responsible for the pollution in Suzhou. The successful implementation of SPI–TOFMS has demonstrated a promising methodology that is well-suited for the real-time and online monitoring of VOCs in the atmosphere. In addition, a library for identifying VOC fingerprints from the same plant was established. This library serves as a comprehensive resource for establishing on-site VOC traceability, estimating source apportionment, and evaluating their impact on ozone formation.

Causes of Summer Ozone Pollution Events in Jinan, East China: Local Photochemical Formation or Regional Transport?

Simultaneous measurements of atmospheric volatile organic compounds (VOCs), conventional gases and meteorological parameters were performed at an urban site in Jinan, East China, in June 2021 to explore the formation and evolution mechanisms of summertime ozone (O3) pollution events. O3 Episode Ⅰ, O3 Episode II, and non-O3 episodes were identified based on the China Ambient Air Quality Standards and the differences in precursor concentrations. The O3 concentrations in Episode I and Episode II were 145.4 μg/m3 and 166.4 μg/m3, respectively, which were significantly higher than that in non-O3 episode (90 μg/m3). For O3 precursors, VOCs and NOx concentrations increased by 48% and 34% in Episode I, and decreased by 21% and 27% in Episode II compared to non-O3 episode days. The analysis of the m,p-xylene to ethylbenzene ratio (X/E) and OH exposure demonstrated that the aging of the air masses in Episode II was significantly higher than the other two episodes, and the differences could not be explained by localized photochemical consumption. Therefore, we speculate that the high O3 concentrations in Episode II were driven by the regional transport of O3 and its precursors. Backward trajectory simulations indicated that the air masses during Episode II were concentrated from the south. In contrast, the combination of high precursor concentrations and favorable meteorological conditions (high temperatures and low humidity) led to an excess of O3 in Episode I. Positive matrix factorization (PMF) model results indicated that increased emissions from combustion and gasoline vehicle exhausts contributed to the elevated concentrations of VOCs in Episode I, and solvent usage may be an important contributor to O3 formation. The results of this study emphasize the importance of strengthening regional joint control of O3 and its precursors with neighboring cities, especially in the south, which is crucial for Jinan to mitigate O3 pollution.

Ozone alters the chemical signal required for plant – insect pollination: The case of the Mediterranean fig tree and its specific pollinator

Tropospheric ozone (O3) is likely to affect the chemical signal emitted by flowers to attract their pollinators through its effects on the emission of volatile organic compounds (VOCs) and its high reactivity with these compounds in the atmosphere. We investigated these possible effects using a plant-pollinator interaction where the VOCs responsible for pollinator attraction are known and which is commonly exposed to high O3 concentration episodes: the Mediterranean fig tree (Ficus carica) and its unique pollinator, the fig wasp (Blastophaga psenes). In controlled conditions, we exposed fig trees bearing receptive figs to a high-O3 episode (5 h) of 200 ppb and analyzed VOC emission. In addition, we investigated the chemical reactions occurring in the atmosphere between O3 and pollinator-attractive VOCs using real-time monitoring. Finally, we tested the response of fig wasps to the chemical signal when exposed to increasing O3 mixing ratios (0, 40, 80, 120 and 200 ppb). The exposure of the fig tree to high O3 levels induced a significant decrease in leaf stomatal conductance, a limited change in the emission by receptive figs of VOCs not involved in pollinator attraction, but a major change in the relative abundances of the compounds among pollinator-attractive VOCs in O3-enriched atmosphere. Fig VOCs reacted with O3 in the atmosphere even at the lowest level tested (40 ppb) and the resulting changes in VOC composition significantly disrupted the attraction of the specific pollinator. These results strongly suggest that current O3 episodes are probably already affecting the interaction between the fig tree and its specific pollinator.

The Role of Catalytic Converter in Vehicles

Liquefied petroleum gas (LPG), diesel, and petrol are utilized in large numbers as energy sources for various vehicles in Afghanistan. Vehicles running on LPG are increasingly the primary source of ambient volatile organic compounds. Long-term observations revealed that the catalytic converter was quite effective in reducing the levels of nitric oxide (NO), NOx, and volatile organic compounds (VOCs) linked to LPG in the air. Catalytic materials are used in car silencers to stop dangerous compounds from burning fuels in engines that cause air pollution, which poses a threat to human health. The role of car silencers is very important to the cleanliness of the environment because these silencers can protect the environment from harmful gases or change more harmful gases into less harmful gases. Those silencers that do not have a catalytic converter in them cause air pollution. Afghanistan's influence is spreading globally, releasing harmful gases into the atmosphere. To reduce these, transport equipment silencers are needed. Carbon monoxide, nitrogen oxides, and partially burned hydrocarbon components can be converted into less harmful substances. Catalysts aim to reduce toxic gases, such as volatile organic hydrocarbons, carbon monoxide, and nitrogen oxides that are created when fossil fuels are not burned completely.

Cruise observation of ambient volatile organic compounds over Hong Kong coastal water

Air pollution is a major environmental issue in Hong Kong, and ozone (O3) is one of the most concerned pollutants because of its notable rising trend during the past three decades. Volatile organic compounds (VOCs) are the main precursors to O3 formation, but their characteristics over coastal water in Hong Kong were not well studied due to a lack of observations. We conducted sixteen cruise campaigns and collected 109 VOC canister samples over Hong Kong coastal water between August 2020 and July 2021. 95 VOC species were analyzed from the samples by a GC-MSD/ECD/FID system to investigate their concentration distributions, reactivities, and potential emission sources. The average concentrations of alkanes, alkenes, aromatics, alkynes, halocarbons, and alkyl nitrates over Hong Kong coastal water were 8.94 ± 5.64 ppbv, 1.18 ± 1.09 ppbv, 1.90 ± 1.48 ppbv, 1.05 ± 0.63 ppbv, 3.82 ± 1.23 ppbv, and 0.09 ± 0.04 ppbv, respectively. Source apportionment results from positive matrix factorization (PMF) analysis suggest that liquefied petroleum gas (LPG) usage (24.9%), biomass burning (19.4%), gasoline evaporation (16.2%), ship emissions (15.6%), solvent usage (14.8%), and aged air mass (9.1%) were main VOC sources over Hong Kong coastal water during the study period. Toluene, ethene and m + p-xylene were found to be the top contributors to the O3 formation over Hong Kong coastal water, while isoprene had less O3 formation contributions compared with land measurements. This study provides important insights into the reactivities and sources of VOCs over Hong Kong coastal water and serves as a stepping stone to understanding the VOC characteristics and O3 formation mechanisms in a complex coastal environment.

Composition and Reactivity of Volatile Organic Compounds and the Implications for Ozone Formation in the North China Plain

Enhanced ozone (O3) pollution has emerged as a pressing environmental concern in China, particularly for densely populated megacities and major city clusters. However, volatile organic compounds (VOCs), the key precursors to O3 formation, have not been routinely measured. In this study, we characterize the spatial and temporal patterns of VOCs and examine the role of VOCs in O3 production in five cities (Dongying (DY), Rizhao (RZ), Yantai (YT), Weihai (WH), and Jinan (JN)) in the North China Plain (NCP) for two sampling periods (June and December) in 2021 through continuous field observations. Among various VOC categories, alkanes accounted for the largest proportion of VOCs in the cities. For VOCs, chemical reactivities, aromatic hydrocarbons, and alkenes were dominant contributors to O3 formation potential (OFP). Unlike inland regions, the contribution to OFP from OVOCs increased greatly at high O3 concentrations in coastal regions (especially YT). Model simulations during the O3 episode show that the net O3 production rates were 27.87, 10.24, and 10.37 ppbv/h in DY, RZ, and JN. The pathway of HO2 + NO contributed the most to O3 production in JN and RZ, while RO2 + NO was the largest contributor to O3 production in DY. The relative incremental reactivity (RIR) revealed that O3 formation in DY was the transitional regime, while it was markedly the VOC-limited regime in JN and RZ. The O3 production response is influenced by NOx concentration and has a clear daily variation pattern (the sensitivity is greater from 15:00 to 17:00). The most efficiencies in O3 reduction could be achieved by reducing NOx when the NOx concentration is low (less than 20 ppbv in this study). This study reveals the importance of ambient VOCs in O3 production over the NCP and demonstrates that a better grasp of VOC sources and profiles is critical for in-depth O3 regulation in the NCP.

Pollution Characteristics，Source Analysis，and Activity Analysis of Atmospheric VOCs During Winter and Summer Pollution in Zhengzhou

In order to study the pollution characteristics of volatile organic compounds （VOCs）， continuous monitoring of VOCs in two pollution processes was conducted in June and December 2021 in Zhengzhou. Combined with meteorological conditions， the pollution characteristics， source contributions， and reactivity of VOCs in winter and summer were compared and analyzed. The results showed that the volume fraction of atmospheric VOCs in two episodes were （27.92±12.68）×10-9 and （24.30±5.93）×10-9， respectively. The volume fraction of atmospheric VOCs in the haze pollution process in winter was larger than that in the ozone pollution process in summer. The analysis results of winter sources were as follows： industrial source （27.0%）， motor vehicle source （22.5%）， combustion source （20.1%）， solvent use source （16.3%）， and oil and gas volatilization source （14.1%）. The analysis results of summer sources were as follows： motor vehicle source （24.8%）， industrial source （24.1%）， solvent source （17.4%）， oil and gas volatilization source （14.2%）， combustion source （11.2%）， and plant source （8.4%）. The results of the smog production model showed that the proportion of days in the synergistic control zone of VOCs during the two pollution processes in summer （66.7%） was smaller than that in winter （100.0%）. The secondary reaction activity results showed that the average ·OH loss rate （L·OH） values in winter and summer were 4.12 s-1 and 4.75 s-1， respectively. The average ozone formation potential （OFP） values in summer were 108.36 μg·m-3. The olefins were dominant in the top ten species due to L·OH and OFP contributions in summer. The total SOAFP values in winter in Zhengzhou were 54.38 μg·m-3. Among the top ten species contributing to SOAFP in winter， nine were aromatic hydrocarbons.

Identifying and correcting interferences to PTR-ToF-MS measurements of isoprene and other urban volatile organic compounds

Abstract. Proton-transfer-reaction time-of-flight mass spectrometry (PTR-ToF-MS) is a technique commonly used to measure ambient volatile organic compounds (VOCs) in urban, rural, and remote environments. PTR-ToF-MS is known to produce artifacts from ion fragmentation, which complicates the interpretation and quantification of key atmospheric VOCs. This study evaluates the extent to which fragmentation and other ionization processes impact urban measurements of the PTR-ToF-MS ions typically assigned to isoprene (m/z 69, C5H8H+), acetaldehyde (m/z 45, CH3CHO+), and benzene (m/z 79, C6H6H+). Interferences from fragmentation are identified using gas chromatography (GC) pre-separation, and the impact of these interferences is quantified using ground-based and airborne measurements in a number of US cities, including Las Vegas, Los Angeles, New York City, and Detroit. In urban regions with low biogenic isoprene emissions (e.g., Las Vegas), fragmentation from higher-carbon aldehydes and cycloalkanes emitted from anthropogenic sources may contribute to m/z 69 by as much as 50 % during the day, while the majority of the signal at m/z 69 is attributed to fragmentation during the night. Interferences are a higher fraction of m/z 69 during airborne studies, which likely results from differences in the reactivity between isoprene and the interfering species along with the subsequent changes to the VOC mixture at higher altitudes. For other PTR masses, including m/z 45 and m/z 79, interferences are observed due to fragmentation and O2+ ionization of VOCs typically used in solvents, which are becoming a more important source of anthropogenic VOCs in urban areas. We present methods to correct these interferences, which provide better agreement with GC measurements of isomer-specific molecules. These observations show the utility of deploying GC pre-separation for the interpretation PTR-ToF-MS spectra.