Sources Of Volatile Organic Compounds Research Articles

Volatile organic compound fluxes in the agricultural San Joaquin Valley – spatial distribution, source attribution, and inventory comparison

Abstract. The San Joaquin Valley is an agricultural region in California that suffers from poor air quality. Since traffic emissions are decreasing, other sources of volatile organic compounds (VOCs) are gaining importance in the formation of secondary air pollutants. Using airborne eddy covariance, we conducted direct, spatially resolved flux observations of a wide range of VOCs in the San Joaquin Valley during June 2021 at 23–36 ∘C. Through land-cover-informed footprint disaggregation, we were able to attribute emissions to sources and identify tracers for distinct source types. VOC mass fluxes were dominated by alcohols, mainly from dairy farms, while oak isoprene and citrus monoterpenes were important sources of reactivity. Comparisons with two commonly used inventories showed that isoprene emissions in the croplands were overestimated, while dairy and highway VOC emissions were generally underestimated in the inventories, and important citrus and biofuel VOC point sources were missing from the inventories. This study thus presents unprecedented insights into the VOC sources in an intensive agricultural region and provides much needed information for the improvement of inventories, air quality predictions, and regulations.

Effect of Volatile Organic Compounds on the Neurobehavioral Functions of Painters in Chennai, Tamilnadu: A Cross Sectional Study

Background: Paints are a major source of volatile organic compounds (VOCs) among painters. Limited information is available on neurobehavioral effect of long-term exposure to VOCs among painters working in unorganised industrial sectors such as construction site. Hence, this study was conducted to evaluate the neurobehavioral impact of long-term exposure to VOCs among construction painters. Methods: This cross-sectional study was conducted among male painters in Chennai. VOC exposure index was calculated using questionnaire as well as personal exposure monitors. Neurobehavioral tests including hand dexterity, auditory (ART) and visual reaction time (VRT) were used to assess motor coordination, fine motor activity, focused attention, and psychomotor speed. Results: Prevalence of prolonged ART and VRT in painters was 69% and 73%, respectively and 65% exhibited reduced hand dexterity. Hand dexterity had mild negative correlation (r = -0.3, p = 0.01) with VOC exposure index and work experience (r = -0.3, p = 0.02), whereas VRT had mild positive correlation (r = 0.3, p = 0.01) with VOC exposure index. Independent t-test showed a significant decrease in motor coordination with higher VOC exposure index (≤ 18.5*103 ppm-hrs = 60.1 ±10.1, >18.5*103 ppm-hrs = 53.3 ±12.3, p=0.03) and increase in work experience (≤ 10 years = 58.8 ±11.6, >10years = 52.5 ±11.5, p=0.05). Conclusion: Neurobehavioral functions gradually decline with VOC exposure in painters working in unorganized sectors indicating a need to create awareness among the public and workers in unorganized sectors about the organic solvent-induced neurobehavioral changes.

Effects of VOC emissions from chemical industrial parks on regional O3-PM2.5 compound pollution in the Yangtze River Delta

Ozone (O3) and fine particulate matter (PM2.5) compound pollution has emerged as a primary form of air pollution in Chinese urban. Volatile organic compounds (VOCs), as common precursors of O3 and PM2.5, play a significant role in air pollution control. Chemical industrial parks (CIPs) are crucial emission sources of VOCs and have garnered significant attention. This study focused on 142 CIPs located in the Yangtze River Delta (YRD) to investigate the characteristics of VOC emissions from CIPs and their impact on O3-PM2.5 compound pollution, considering the enhanced atmospheric oxidation capacity (AOC). The Comprehensive Air Quality Model with Extensions (CAMx) model was employed for this analysis. The results show that VOC emissions from CIPs contributed significantly to regional O3 and secondary organic aerosol (SOA), accounting for 17.1 % and 18.18 % of the anthropogenic sources, respectively. Regions exhibiting the highest contributions were located along the Hangzhou Bay. Compared with 2014, an elevation in the contribution of VOC emissions from CIPs to the annual average concentrations of MDA8 O3 and SOA in the YRD in 2017 by 0.069 μg/m3 and 0.007 μg/m3, respectively. During episodes of compound pollution, the concentration of atmospheric oxidant (HOx + NO3) was 28.65 % higher than during clean days, and significant positive correlations were observed between hydrogen oxygen radicals (HOx) and maximum daily 8-h average (MDA8 O3) as well as between HOx and SOA, exhibiting correlation coefficients of 0.86 and 0.48, respectively. Effective control measures for VOC emissions, particularly from the pharmaceutical and petrochemical industry parks located along Hangzhou Bay, are essential in curtailing the production rate of HOx and in regulating AOC levels in the YRD. Maintaining the daily average HOx concentration below 10 ppt would be a valuable strategy in achieving coordinated control of O3 and SOA, thus aiding in the alleviation of O3-PM2.5 compound pollution in the YRD.

Identification of volatile organic compounds and their sources driving ozone and secondary organic aerosol formation in NE Spain

Volatile organic compounds (VOCs) play a crucial role in the formation of ozone (O3) and secondary organic aerosol (SOA). We conducted measurements of VOC ambient mixing ratios during both summer and winter at two stations: a Barcelona urban background station (BCN) and the Montseny rural background station (MSY). Subsequently, we employed positive matrix factorization (PMF) to analyze the VOC mixing ratios and identify their sources. Our analysis revealed five common sources: anthropogenic I (traffic & industries); anthropogenic II (traffic & biomass burning); isoprene oxidation; monoterpenes; long-lifetime VOCs. To assess the impact of these VOCs on the formation of secondary pollutants, we calculated the ozone formation potential (OFP) and secondary organic aerosol formation potential (SOAP) associated with each VOC. In conclusion, our study provides insights into the sources of VOCs and their contributions to the formation of ozone and SOA in NE Spain. The OFP was primarily influenced by anthropogenic aromatic compounds from the traffic & industries source at BCN (38–49 %) and during winter at MSY (34 %). In contrast, the summer OFP at MSY was primarily driven by biogenic contributions from monoterpenes and isoprene oxidation products (45 %). Acetaldehyde (10–35 %) and methanol (13–14 %) also made significant OFP contributions at both stations. Anthropogenic aromatic compounds originating from traffic, industries, and biomass burning played a dominant role (88–93 %) in SOA formation at both stations during both seasons. The only exception was during the summer at MSY, where monoterpenes became the primary driver of SOA formation (41 %). These findings emphasize the importance of considering both anthropogenic and biogenic VOCs in air quality management strategies.

Impurity contribution to ultraviolet absorption of saturated fatty acids.

Saturated fatty acids are abundant organic compounds in oceans and sea sprays. Their photochemical reactions induced by solar radiation have recently been found as an abiotic source of volatile organic compounds, which serve as precursors of secondary organic aerosols. However, photoabsorption of wavelengths longer than 250 nanometers in liquid saturated fatty acids remains unexplained, despite being first reported in 1931. Here, we demonstrate that the previously reported absorption of wavelengths longer than 250 nanometers by liquid nonanoic acid [CH3(CH2)7COOH)] originates from traces of impurities (0.1% at most) intrinsically contained in nonanoic acid reagents. Absorption cross sections of nonanoic acid newly obtained here indicate that the upper limit of its photolysis rate is three to five orders of magnitude smaller than those for atmospherically relevant carbonyl compounds.

Impact of emissions of volatile organic compounds from restaurants on ambient air quality and health: Case study in beijing

Cooking fumes are important sources of volatile organic compounds (VOCs). Compared with home cooking, commercial cooking uses a higher number of stoves, consumes more oil, operates for longer hours, and performs more complex cooking processes and usage of seasoning, resulting in more serious pollution. In this study, we collected samples of cooking fumes from six common types of restaurants in Beijing, and investigated their emission characteristics. We analyzed the secondary transformations of VOCs in cooking fumes and their impacts on human health. Results show that oxygenated VOCs (O–VOCs) accounted for the highest proportion of VOCs emitted by all types of restaurants (47.67–73.46%), with ethanol being their most significant component (27.04–62.31%). The ozone formation potential (OFP) were the highest from canteen emissions, and secondary organic aerosol potential (SOAP) were the highest from barbecue emissions. Among VOCs, aromatic hydrocarbons contributed the most to atmospheric SOA in all types of restaurants, exceeding 80%. The carcinogenic risks of the Class 1 carcinogens benzene and 1,3-butadiene in VOCs of barbecue emissions were the highest, and did not exceed acceptable levels. The non-carcinogenic risks were high from both barbecue and canteen without exceeding threshold values. This study can serve as an important basis for assessing the contribution of VOCs from restaurants in Beijing to secondary pollutants and their impacts on human health, and lead to the accurate determinations of the focus of pollution control.

Measurement report: Source apportionment and environmental impacts of volatile organic compounds (VOCs) in Lhasa, a highland city in China

Abstract. Hypoxia and adverse health outcomes might be affected by O3 pollution in the highland city of Lhasa. NOx emissions can amplify the role of volatile organic compounds (VOCs) in the secondary production of O3 under the conditions of high ultraviolet (UV) radiation levels and unfavourable dispersion patterns in the Lhasa River valley. Here, online C2–C11 VOC measurements, accompanied by other parameters concerning the O3 chemical budget, were first obtained and employed to identify the key VOC species and key sources of VOCs in terms of the loss rate against OH radicals (LOH), ozone formation potential (OFP), secondary organic aerosol potential (SOAP), and toxicity. Oxygenated VOCs (OVOCs) not only were the most abundant VOCs but also dominated LOH, OFP, and toxicity. Isoprene and anthropogenic VOCs were further identified as precursors of these OVOCs. Aromatics accounted for 5 % of the total VOCs (TVOCs) but contributed 88 % to the SOAP and 10 % to the toxicity. As the primary oxidative intermediates of aromatics were not well characterized by our measurements, the environmental impact of aromatics could be underestimated by our data. Source appointment and ternary analysis of benzene, toluene, and ethylbenzene confirmed the combined contribution of traffic emissions, solvent usage, and biomass burning. This suggests that O3 precursors are mainly from sources associated with residents' lives, except for solvent usage emissions which contribute to aromatics. Preliminary comparisons between source spectrums of transport sector emissions with positive matrix factorization (PMF)-decomposed ones and our measured ones suggest that vehicle emission patterns of VOCs at high altitude generally follow the ground-level impression. More quantitative data are required to further confirm this point though. Emission reduction strategy analysis for O3 pollution control highlighted multiple benefits of the simultaneous reduction in NOx originating from diesel vehicle emissions, biomass burning, and background sources (possibly dominated by incense burning). The notable biogenic emission contribution to the OFP was also first confirmed in our study, and this highlights the side effects of the government's pursuit of a greener city.

Composition Characteristics of VOCs in the Atmosphere of the Beibei Urban District of Chongqing: Insights from Long-Term Monitoring

Reducing anthropogenic volatile organic compounds (VOCs) is the most effective way to mitigate O3 pollution, which has increased over the past decades in China. From 2012 to 2017, special stainless-steel cylinders were used to collect ambient air samples from the urban area of Beibei district, Chongqing. Three-step pre-concentration gas chromatography–mass spectrometry was used to detect the collected air samples. The composition, concentration, photochemical reactivity, and sources of VOCs in Beibei were analyzed. During the observation period, the annual average VOC concentration was 31.3 ppbv, which was at an intermediate range compared to other cities in China. Alkanes (36.8%) and aromatics (35.6%) were the most abundant VOC groups, followed by halo-hydrocarbons (14.4%) and alkenes (12.6%). The overall trend of seasonal distribution of VOC concentration was high in summer and autumn, and low in winter and spring, with a statistically significant difference between summer and winter concentrations. The ozone formation potential (OFP) showed that alkenes were the most active species, followed by aromatics and alkanes, and summer was the season with the highest OFP (131.6 ppbv). Three major emission sources were identified through principal component analysis (PCA), i.e., vehicle exhaust emissions (66.2%), fuel oil evaporation (24.8%), and industrial sources (9.0%). To ameliorate the air quality within the study area, concerted efforts should be directed towards curtailing traffic emissions and mitigating the release of alkenes, particularly emphasizing more stringent interventions during the summer season.

Characterization of photochemical losses of volatile organic compounds and their implications for ozone formation potential and source apportionment during summer in suburban Jinan, China

Volatile organic compounds (VOCs) undergo substantial photochemical losses during their transport from emission sources to receptor sites, resulting in serious implications for their source apportionment and ozone (O3) formation. Based on the continuous measurements of VOCs in suburban Jinan in August 2022, the effects of photochemical losses on VOC source contributions and O3 formation were evaluated in this study. The observed and initial concentrations of total VOCs (TVOC) were 12.0 ± 5.1 and 16.0 ± 7.4 ppbv, respectively. Throughout the observation period, alkenes had the most prominent photochemical losses (58.2%), followed by aromatic hydrocarbons (23.1%), accounting for 80.6% and 6.9% of the total losses, respectively. During high O3 episodes, the photochemical loss of VOCs was 6.9 times higher than that during the cleaning period. Alkene losses (exceeding 67.3%), specifically losses of isoprene, propylene, ethylene, and n-butene, dominated the total losses of VOCs during the O3 increase period. Eight sources of VOCs were identified by positive matrix factorization (PMF) based on the observed and initial concentration data (OC-PMF and IC-PMF, respectively). Concentrations of all emission sources in the OC-PMF were underestimated by 2.4%–57.1%. Moreover, the contribution of each emission source was over- or underestimated compared with that in case of the IC-PMF. The contributions of biogenic and motor vehicle exhaust emissions were underestimated by 5.3 and 2.8 percentage points, respectively, which was associated with substantial oxidation of the emitted high-reactive species. The contributions of coal/biomass burning and natural gas were overestimated by 2.4 and 3.9 percentage points, respectively, which were related to the emission of low-reactive species (acetylene, ethane, and propane). Based on our results, the photochemical losses of VOCs grossly affect their source apportionment and O3 formation. Thus, photochemical losses of VOCs must be thoroughly accounted to establish a precise scientific foundation for air-pollution control strategies.

Formation of nitrogen-containing gas phase products from the heterogeneous (photo)reaction of NO2 with gallic acid

Heterogeneous reaction of gas phase NO2 with atmospheric humic-like substances (HULIS) is potentially an important source of volatile organic compounds (VOCs) including nitrogen (N)-containing compounds, a class of brown carbon of emerging importance. However, the role of ubiquitous water-soluble aerosol components in this multiphase chemistry, namely nitrate and iron ions, remains largely unexplored. Here, we used secondary electrospray ionization ultrahigh-resolution mass spectrometry for real-time measurements of VOCs formed during the heterogeneous reaction of gas phase NO2 with a solution containing gallic acid (GA) as a proxy of HULIS at pH 5 relevant for moderately acidic aerosol particles. Results showed that the number of detected N-containing organic compounds largely increased from 4 during the NO2 reaction with GA in the absence of nitrate and iron ions to 55 in the presence of nitrate and iron ions. The N-containing compounds have reduced nitrogen functional groups, namely amines, imines and imides. These results suggest that the number of N-containing compounds is significantly higher in deliquescent aerosol particles due to the influence of relatively higher ionic strength from nitrate ions and complexation/redox reactivity of iron cations compared to that in the dilute aqueous phase representative of cloud, fog, and rain water.

Volatile organic compounds during routine production and planned shutdown of a petrochemical refinery: Emission characteristics, source and risk assessment

During the routine production and planned shutdown of a petrochemical refinery in China, ambient volatile organic compound (VOC) data were continuously determined by an online monitoring system, and VOC characteristics, source apportionment, and health risks were calculated based on those data. The data showed that the total VOC concentration emitted during the planned shutdown period was significantly higher than that under daily production conditions, especially the alkane concentration, which increased from 137.4 μg m−3 to 481.8 μg m−3. A source apportionment study was performed using a positive matrix factorization model based on VOC data collected during different sampling times. The contributions of petroleum refinery emissions increased from 63.8% during routine production to 79.4% during the shutdown period. In addition, carcinogenic and noncarcinogenic risk assessment revealed that workers could be under higher acute and chronic health risks during the shutdown and maintenance period than during the routine production of the refinery. The results also indicated that VOCs emitted during maintenance might have more influence on public health. Therefore, more attention should be paid to the emission characteristics and source apportionment of VOCs during planned shutdowns. This work provides valuable data that can help regulatory agencies formulate VOC control strategies during routine production and shutdown maintenance in petrochemical refineries.

Spatiotemporal distribution, source apportionment and health risk assessment of atmospheric volatile organic compounds using passive air samplers in a typical coastal area, China

To fully understand source characteristics and human health effects of atmospheric volatile organic compounds (VOCs), it is of great importance to implement long-term measurements, precise source apportionment and simulation. In this study, a 12-month measurement of VOCs was conducted in a coastal area in East China by a novel passive air sampler (PAS). A total of 28 VOC species, mainly in groups of aromatics and halohydrocarbons were observed. The monthly average concentrations of TVOC were as follows: industrial sites (154.10–727.19 μg m−3) > business sites (65.83–86.96 μg m−3) > residential sites (59.63–60.05 μg m−3) > background site (57.62 μg m−3). Their seasonal variation characteristics were: winter > spring > autumn > summer, which was more apparent at industrial sites due to human activities. Six VOC sources including industrial processes, organic solvents, dyeing, plastic synthesis, traffic emissions, and pesticides identified by the positive matrix factorization model compared favorably with the local emissions at industrial sites. Bromoform, hexachloro-1,3-butadiene, C1–C3 halogenated alkanes and benzene homologs could be the important indicators of industrial VOC emissions. The halohydrocarbons and aromatics were the major contributors to the ozone formation potential (OFP) and secondary organic aerosol potential (SOAP) in industrial areas, respectively. Both of OFP and SOAP have their maximum values in winter due to high VOC concentrations. Health risk assessment indicated that a high probability of non-carcinogenic risk (HI > 1) was in the region at 10 m height and 50m radius, and minor carcinogenic risk (CR > 10−6) was in the region at 70 m height and 1000 m radius. Among all the compounds, 1,2-Dibromo-3-chloropropane was the largest contributor with the individual HI value (17.99) and carcinogenic risk (5.34 × 10−3) at the peak. In this study, the PAS as a sampling tool was proven to be reliable and efficient for long-term measurements in coastal areas. It is worth to have further studies to promote passive sampling as an alternative to VOCs monitoring methods.

Effects of drought and recovery on soil volatile organic compound fluxes in an experimental rainforest

Drought can affect the capacity of soils to emit and consume biogenic volatile organic compounds (VOCs). Here we show the impact of prolonged drought followed by rewetting and recovery on soil VOC fluxes in an experimental rainforest. Under wet conditions the rainforest soil acts as a net VOC sink, in particular for isoprenoids, carbonyls and alcohols. The sink capacity progressively decreases during drought, and at soil moistures below ~19%, the soil becomes a source of several VOCs. Position specific 13C-pyruvate labeling experiments reveal that soil microbes are responsible for the emissions and that the VOC production is higher during drought. Soil rewetting induces a rapid and short abiotic emission peak of carbonyl compounds, and a slow and long biotic emission peak of sulfur-containing compounds. Results show that, the extended drought periods predicted for tropical rainforest regions will strongly affect soil VOC fluxes thereby impacting atmospheric chemistry and climate.

Soil uptake of VOCs exceeds production when VOCs are readily available

Volatile organic compounds (VOCs) are reactive gaseous compounds with significant impacts on air quality and the Earth's radiative balance. While natural ecosystems are known to be major sources of VOCs, primarily due to vegetation, soils, an important component of these ecosystems, have received relatively less attention as potential sources and sinks of VOCs. In this study, soil samples were collected from two temperate ecosystems: a beech forest and a heather heath, and then sieved, homogenized, and incubated under various controlled conditions such as different temperatures, oxic vs. anoxic conditions, and different ambient VOC levels. A dynamic flow-through system coupled to a proton transfer reaction-time of flight-mass spectrometry (PTR-ToF-MS) was used to measure production and/or uptake rates of selected VOCs, aiming to explore the processes and their controlling mechanisms. Our results showed that these soils were natural sources of a variety of VOCs, and the strength and profile of these emissions were influenced by soil properties (e.g. moisture, soil organic matter), oxic/anoxic conditions, and temperature. The soils also acted as sinks for most VOCs when VOC substrates at parts per billions levels (ranging between 0.18 and 68.65 ppb) were supplied to the headspace of the enclosed soils, and the size of the sink corresponded to the amount of VOCs available in the ambient air. Temperature-controlled incubations and glass bead simulations indicated that the uptake of VOCs by soils was likely driven by microbial metabolism, with a minor contribution from physical adsorption to soil particles. In conclusion, our study suggests that soil uptake of VOCs can mitigate the impact of other significant VOC sources in the near-surface environment and potentially regulate the net exchange of these trace gases in ecosystems.

Atmospheric oxidation capacity and secondary pollutant formation potentials based on photochemical loss of VOCs in a megacity of the Sichuan Basin, China

Volatile organic compounds (VOCs) are significant precursors to photochemical pollution. However, reactive VOC species are easily oxidized during transportation, resulting in a systematic underestimate of the measured concentrations. To address this, we applied an improved calculation method to correct the measured VOC concentrations into photochemical initial concentrations (PICs) in Chengdu, a megacity in the Sichuan Basin, China, which is highly vulnerable to complex pollution. In this study, 56 VOC species on the Photochemical Assessment Monitor Station (PAMS) target list were quantitatively monitored throughout all four seasons. Comparing to directly measured values, photochemically initialized total mixing ratios of VOCs increased by 18.6 % in general. The photochemical loss percentages of alkenes and aromatics were prominent in summer (68.6 %, 28.7 %) and spring (65.9 %, 24.7 %), respectively. Furthermore, we examined contributions of VOCs to atmospheric oxidation capacity (AOC) depending on PICs and found that maximum daily total AOC showed a surge in spring and summer. Besides hydroxyl radicals, daytime O3 in spring and late-afternoon nitrate radicals in summer were essential for AOC with PICs. As expected, alkenes and aromatics dominated PIC-based ozone formation potentials (OFPs). Furthermore, contribution of alkenes to secondary organic aerosol formation potentials reached 15.5 % and 7.6 % in spring and summer, respectively. Using positive matrix factorization model, we identified five VOC sources including vehicular exhaust, industrial emissions, solvent usage, biogenic sources, and liquefied petroleum gas/natural gas use. Based on PICs, biogenic sources were significantly underestimated in spring and summer. Meanwhile, m,p-xylene from solvent usage and isoprene from biogenic sources were the primary contributors to OFPs. Consequently, these results emphasize the significance of photochemically oxidized VOC concentrations, especially for reactive species in typical seasons.

Characterizing VOCs emissions of five packaging and printing enterprises in China and the emission reduction potential of this industry

The packaging and printing industry has become an important source of industrial volatile organic compounds (VOCs) emissions in China, due to the abundant consumption of organic materials. Effective control measures must be developed which rely on a comprehensive understanding of both current emission characteristics and future emission projections. However, representative VOCs source profiles and updated EFs of packaging and printing industry in China are still lacking. In order to fully explore the VOCs emissions characteristics of packaging and printing industry, field measurements including 17 processes in five packaging and printing factories were conducted in this study. The emission factors (EFs), VOCs source profiles, ozone formation potential (OFP) and secondary organic aerosols potential (SOAP) of 110 VOCs species were acquired. Speciated VOCs emission inventory of packaging and printing industry was compiled based on the activity data in 2020. The future reduction perspectives of packaging and printing industry in China were projected. The VOCs EFs of different materials were estimated, including solvent-based ink (287 g/kg), water-based ink (117 g/kg), soybean oil ink (44 g/kg), UV curing ink (22 g/kg), solvent-based adhesive (420 g/kg), and water-based adhesive (139 g/kg). The VOCs EFs of products were 35.58 kg/t for plastic wrapper, 7.28 g/m2 for soft package plastic, 0.083 g/piece for carton, 0.54 g/piece for tin case, and 0.14 g/piece for aluminum can. The total VOCs emissions in Chinese packaging and printing industry was estimated to 634.32 Gg in 2020. Guangdong, Zhejiang, Jiangsu, Fujian, Shandong, and Sichuan contributed 73% to total VOCs emissions. Printing workshop was the main contributor to both primary emission and secondary pollutant generation. OVOCs was the most abundant specie in three sub-industries. The key VOCs species in PF were ethylacetate, ethanol, 2-pentanone, methyl ethyl ketone, and i-propanol. I-propanol, ethanol, m-tolualdehyde, and dichloromethane were dominated in PP. Ethanol, m/p-xylene, i-propanol, o-xylene, and acetaldehyde were the key species in MC. The key VOCs species to OFP and SOAP were ethanol, methyl ethyl ketone, 2-pentanone, ethyl methacrylate, acetaldehyde, toluene, and xylene, which should be prioritized. The VOCs emissions would be reduced by 46.5% in 2025 and 66.4% in 2030 with stringent control measures. Increasing the usage proportion of low-VOCs-contained raw material and improving treatment efficiency are the key technologies to reduce the VOCs emissions in the packaging and printing industry.

Leaf-level metabolic changes in response to drought affect daytime CO2 emission and isoprenoid synthesis pathways.

In the near future, climate change will cause enhanced frequency and/or severity of droughts in terrestrial ecosystems, including tropical forests. Drought responses by tropical trees may affect their carbon use, including production of volatile organic compounds (VOCs), with implications for carbon cycling and atmospheric chemistry that are challenging to predict. It remains unclear how metabolic adjustments by mature tropical trees in response to drought will affect their carbon fluxes associated with daytime CO2 production and VOC emission. To address this gap, we used position-specific 13C-pyruvate labeling to investigate leaf CO2 and VOC fluxes from four tropical species before and during a controlled drought in the enclosed rainforest of Biosphere 2 (B2). Overall, plants that were more drought-sensitive had greater reductions in daytime CO2 production. Although daytime CO2 production was always dominated by non-mitochondrial processes, the relative contribution of CO2 from the tricarboxylic acid cycle tended to increase under drought. A notable exception was the legume tree Clitoria fairchildiana R.A. Howard, which had less anabolic CO2 production than the other species even under pre-drought conditions, perhaps due to more efficient refixation of CO2 and anaplerotic use for amino acid synthesis. The C. fairchildiana was also the only species to allocate detectable amounts of 13C label to VOCs and was a major source of VOCs in B2. In C. fairchildiana leaves, our data indicate that intermediates from the mevalonic acid (MVA) pathway are used to produce the volatile monoterpene trans-β-ocimene, but not isoprene. This apparent crosstalk between the MVA and methylerythritol phosphate pathways for monoterpene synthesis declined with drought. Finally, although trans-β-ocimene emissions increased under drought, it was increasingly sourced from stored intermediates and not de novo synthesis. Unique metabolic responses of legumes may play a disproportionate role in the overall changes in daytime CO2 and VOC fluxes in tropical forests experiencing drought.

Ambient Volatile Organic Compound Characterization, Source Apportionment, and Risk Assessment in Three Megacities of China in 2019.

In order to illustrate pollution characterization, source apportionment, and risk assessment of VOCs in Beijing, Baoding, and Shanghai, field observations of CO, NO, NO2, O3, and volatile organic compounds (VOCs) were conducted in 2019. Concentrations of VOCs were the highest in Beijing (105.4 ± 52.1 ppb), followed by Baoding (97.1 ± 47.5 ppb) and Shanghai (91.1 ± 41.3 ppb). Concentrations of VOCs were the highest in winter (120.3 ± 61.5 ppb) among the three seasons tested, followed by summer (98.1 + 50.8 ppb) and autumn (75.5 + 33.4 ppb). Alkenes were the most reactive VOC species in all cities, accounting for 56.0%, 53.7%, and 39.4% of ozone formation potential in Beijing, Baoding, and Shanghai, respectively. Alkenes and aromatics were the reactive species, particularly ethene, propene, 1,3,5-trimethylbenzene, and m/p-xylene. Vehicular exhaust was the principal source in all three cities, accounting for 27.0%, 30.4%, and 23.3% of VOCs in Beijing, Baoding, and Shanghai, respectively. Industrial manufacturing was the second largest source in Baoding (23.6%) and Shanghai (21.3%), and solvent utilization was the second largest source in Beijing (25.1%). The empirical kinetic modeling approach showed that O3 formation was limited by both VOCs and nitric oxides at Fangshan (the suburban site) and by VOCs at Xuhui (the urban site). Acrolein was the only substance with an average hazard quotient greater than 1, indicating significant non-carcinogenic risk. In Beijing, 1,2-dibromoethane had an R-value of 1.1 × 10-4 and posed a definite carcinogenic risk.

Source apportionment of consumed volatile organic compounds in the atmosphere

Conventional source apportionments of ambient volatile organic compounds (VOCs) have been based on observed and initial concentrations after photochemical correction. However, these results have not been related to ozone (O3) and secondary organic aerosol (SOA) formation. Thus, the apportioned contributions could not effectively support secondary pollution control development. Source apportionment of the VOCs consumed in forming O3 and SOA is needed. A consumed VOC source apportionment approach was developed and applied to hourly speciated VOCs data from June to August 2022 measured in Laoshan, Qingdao. Biogenic emissions (56.3%), vehicle emissions (17.2%), and gasoline evaporation (9.37%) were the main sources of consumed VOCs. High consumed VOCs from biogenic emissions mainly occurred during transport from parks to the southwest and northwest of study site. During the O3 pollution period, biogenic emissions (46.3%), vehicle emissions (24.2%), and gasoline evaporation (14.3%) provided the largest contributions to the consumed VOCs. However, biogenic emissions contribution increased to 57.1% during the non-O3 pollution period, and vehicle emissions and gasoline evaporation decreased to 16.5% and 9.01%, respectively. Biogenic emissions and the mixed source of combustion sources and solvent use contributed the most to O3 and SOA formation potentials during the O3 pollution period, respectively.

Composition Characteristics of Volatile Organic Compounds and Associated Contributions to Secondary Pollution in Shenyang Industrial Area in Summer

Based on the observation data of volatile organic compounds (VOCs) in the industrial area of Shenyang during the summer of 2019 and 2020, the composition characteristics and sources of VOCs were preliminarily studied. The ozone formation potential (OFP) and aerosol formation potential (AFP) of VOCs were also estimated using the max incremental reactivity (MIR) and aerosol formation coefficient (FAC) methods, respectively. The results showed that the average concentration of VOCs was 41.66 μg·m-3, and the proportions of alkanes, olefins, aromatics, and acetylene were 48.50%, 14.08%, 15.37%, and 22.05%, respectively. The top ten species of VOCs were primarily C2-C5 alkanes, also including acetylene, ethylene, and some aromatics, accounting for 69.25% of the total VOCs. VOCs showed obvious diurnal variation characteristics with a high concentration in the morning and evening (at 06:00 and 22:00) and a low concentration in the afternoon (11:00-16:00). According to the value of toluene/benzene (T/B) and isopentane/n-pentane, the atmosphere of the industrial area was mainly affected by vehicle exhaust emissions, solvent use, combustion sources, and LPG/NG. The total AFP of VOCs was up to 41.43×10-2 μg·m-3, and aromatics were the largest contributor. The total OFP of VOCs reached 117.59 μg·m-3, in which the alkenes contributed the most.