Group Of Volatile Organic Compounds Research Articles

Probing Into Ozone Production Through Photochemistry of Organic Peroxyl Radicals: Implications for Source Control

AbstractOzone (O3) pollution is a focus of the international community due to its health and environmental impacts. Organic peroxyl (RO2) radicals play a significant role in O3 initiation processes, which has implications for O3 mitigation. RO2 generated from volatile organic compounds (VOCs) sources contribute substantially to O3 formation. However, quantifying the RO2 from diverse sources is a great challenge. For the first time, we proposed a new hybrid Receptor‐Kinetic model to quantify sources contributions to RO2 from the perspective of molecular level and functional groups of VOCs. We revealed that 3‐Hydroxy‐2‐butylperoxy (BUT2OLO2), 4‐Hydroxy‐3‐methyl‐1‐butene‐3‐ylperoxy (ISOPBO2) and 1‐Hydroxypropane‐2‐ylperoxy (HYPROPO2) radicals were the dominant RO2, which were driven by reactions of cis/trans‐2‐butene (from Biogenic Emissions and Solvent Usage), isoprene (from Biogenic Emissions), and propylene (from Liquid Petroleum Gas Evaporation), respectively. The three dominant RO2 radicals contributed significantly to O3 production (28%, 10% and 14%), comparing with other 16 RO2. Sensitivity studies indicated that O3 production can be decreased effectively by reducing the dominant RO2 species for each source. Quantitative evidence suggested that targeting dominant RO2 sources can be a novel direction for O3 control.

Seasonal estimates of ozone and secondary organic aerosol formation from volatile organic compounds in a rural atmosphere of India

Volatile Organic Compounds (VOCs) serve as precursors for tropospheric ozone (O3) and Secondary Organic Aerosol (SOA) formation. The formation of O3 and SOA are the indicators of the oxidative capacity specific to a given chemical environment. The current study investigates the oxidative capacity of the relatively less explored tropical rural atmosphere. This study is accomplished by measuring the concentrations of various VOCs and combining them with OH loss rates to estimate the potentials for O3 and SOA formation (OFP and SOAP, respectively). Continuous diel VOC measurement data from Gadanki (13.5°N, 79.2°E), Peninsular India, encompassing four distinct seasons and comprising over 4000 samples, have been utilized to estimate OFP and SOAP and their variations across different seasons. Additionally, efforts have been made to comprehend the contribution of different VOC sources to O3 and SOA formation. The results indicate that, 1, 3, 6-trimethyl benzene (20.09 %) among the VOCs and aromatics (44.37%) among the VOC groups exhibit the highest OFP at the observational site. Among seasons, the post-monsoon period exhibits the highest OFP (31.94%). The increased presence of biogenic VOCs, such as ethylene, propylene, and 1-butene during monsoon, likely due to the increased vegetation cover can be attributed for the elevated OFP. Similarly, n-dodecane (43.22%) and the VOC group of alkanes (50.79%) show the highest SOAP. The summer season has the highest SOAP (29.7%), owing to the enhanced concentrations and photochemistry initiated by OH radicals. Within the PMF-modelled sources, biomass-burning VOCs make a substantial contribution to both OFP and SOAP, distinguishing the rural atmosphere from its urban counterpart, where traffic emissions predominantly influence OFP and SOAP.

Enhanced VOC emission with increased temperature contributes to the shift of O3-precursors relationship and optimal control strategy

Assessing the impact of anthropogenic volatile organic compounds (VOCs) on ozone (O3) formation is vital for the management of emission reduction and pollution control. Continuous measurement of O3 and the major precursors was conducted in a typical light industrial city in the YRD region from 1 May to 25 July in 2021. Alkanes were the most abundant VOC group, contributing to 55.0% of TVOCs concentration (56.43 ± 21.10 ppb). OVOCs, aromatics, halides, alkenes, and alkynes contributed 18.7%, 9.6%, 9.3%, 5.2% and 1.9%, respectively. The observational site shifted from a typical VOC control regime to a mixed regime from May to July, which can be explained by the significant increase of ROx production, resulting in the transition of environment from NOx saturation to radical saturation with respect to O3 production. The optimal O3 control strategy should be dynamically changed depending on the transition of control regime. Under NOx saturation condition, minimizing the proportion of NOx in reduction could lead to better achievement of O3 alleviation. Under mixed control regime, the cut percentage gets the top priority for the effectiveness of O3 control. Five VOCs sources were identified: temperature dependent source (28.1%), vehicular exhausts (19.9%), petrochemical industries (7.2%), solvent & gasoline usage (32.3%) and manufacturing industries (12.6%). The increase of temperature and radiation would enhance the evaporation related VOC emissions, resulting in the increase of VOC concentration and the change of ROx circulation. Our results highlight determination of the optimal control strategies for O3 pollution in a typical YRD industrial city.

Spatiotemporal variations, sources, and atmospheric transformation potential of volatile organic compounds in an industrial zone based on high-resolution measurements in three plants

Industrial emissions are significant sources of volatile organic compounds (VOCs). This study conducted a field campaign at high temporal and spatial resolution to monitor VOCs within three plants in an industrial park in southern China. VOC concentrations showed significant spatial variability in this industrial zone, with median concentrations of 75.22, 40.53, and 29.41 μg/m3 for the total VOCs in the three plants, respectively, with oxygenated VOCs (OVOCs) or aromatics being the major VOCs. Spatial variability within each plant was also significant but VOC-dependent. Seasonal variations in the VOC levels were governed by their industrial emissions, meteorological conditions, and photochemical losses, and they were different for the four groups of VOCs. The temporal and spatial variations in the VOC compositions suggest similar sources of each class of VOCs during different periods of the year in each plant. The diurnal patterns of VOCs (unimodal or bimodal) clearly differed from those at most industrial/urban locations previously, reflecting a dependence on industrial activities. The secondary transformation potential of VOCs also varied temporally and spatially, and aromatics generally made the predominant contributions in this industrial park. The loss rate of OH radicals and ozone formation potential were highly correlated, but the linear relationship substantially changed in summer and autumn due to the intensive emissions of an OVOC species. The lifetime cancer and non-cancer risks via occupational inhalation of the VOCs in the plants were acceptable but merit attention. Taking the secondary transformation potential and health risks into consideration, styrene, xylene, toluene, trichloroethylene, and benzene were proposed to be the priority VOCs regulated in the plants.

Elucidating contributions of volatile organic compounds to ozone formation using random forest during COVID-19 pandemic: A case study in China

Ozone has been reported to increase despite nitrogen oxides reductions during the COVID-19 pandemic, and ozone formation needs to be revisited using volatile organic compounds (VOCs), which are rarely measured during the pandemic. Here, a total of 98 VOCs species were monitored in an economy-active city in China from January 2021 to August 2022 to assess contributions to ozone formation during the pandemic. Total VOCs concentrations were 35.55 ± 21.47 ppb during the entire period, among which alkanes account for the largest fraction (13.78 ppb, 38.0%), followed by aromatics (6.16 ppb, 16.8%) and oxygenated VOCs (OVOCs, 5.69 ppb, 15.7%). Most VOCs groups (e.g., alkenes, OVOCs) and individual species (e.g., isoprene, methyl vinyl ketone) display obvious seasonal and diurnal variations, which are related to their sources and reactivities. No weekend effects of VOCs suggest limited influences from traffic emissions during pandemic. Aromatics and alkenes are the major contributors (39% and 33%) to ozone formation potential, largely driven by o/m/p-xylene (21%), ethylene (15%), toluene (9%). Secondary organic aerosol formation potential is dominated by toluene (>50%) despite its low proportion (5%). Further inclusion of VOCs and meteorology in the Random Forest model shows good ozone prediction performance (R2 = 0.77–0.86, RMSE = 11.95–19.91 μg/m3, MAE = 8.89–14.58 μg/m3). VOCs and NO2 contribute >50% of total importance with the largest difference in importance ratio of VOCs/NO2 in the summer and winter, implying ozone formation regime may vary. No seasonal variations in importance of meteorology are observed, while importance of other variables (e.g., PM2.5) is highest in the summer. This work identifies critical VOCs groups and species for ozone formation during the pandemic, and demonstrates the feasibility of machine learning algorithms in elucidation of ozone formation mechanisms.

Enhancement of Benzene Emissions in Special Combinations of Electronic Nicotine Delivery System Liquid Mixtures.

Electronic nicotine delivery systems (ENDS) are battery-powered devices introduced to the market as safer alternatives to combustible cigarettes. Upon heating the electronic liquid (e-liquid), aerosols are released, including several toxicants, such as volatile organic compounds (VOCs). Benzene has been given great attention as a major component of the VOCs group as it increases cancer risk upon inhalation. In this study, several basic e-liquids were tested for benzene emissions. The Aerosol Lab Vaping Instrument was used to generate aerosols from ENDS composed of different e-liquid combinations: vegetable glycerin (VG), propylene glycol (PG), nicotine (nic), and benzoic acid (BA). The tested mixtures included PG, PG + nic + BA, VG, VG + nic + BA, 30/70 PG/VG, and 30/70 PG/VG + nic + BA. A carboxen polydimethylsiloxane fiber for a solid-phase microextraction was placed in a gas cell to trap benzene emitted from a Sub-Ohm Minibox C device. Benzene was adsorbed on the fiber during the puffing process and for an extra 15 min until it reached equilibrium, and then it was determined using gas chromatography-mass spectrometry. Benzene was quantified in VG but not in PG or the 30/70 PG/VG mixtures. However, benzene concentration increased in all tested mixtures upon the addition of nicotine benzoate salt. Interestingly, benzene was emitted at the highest concentration when BA was added to PG. However, lower concentrations were found in the 30/70 PG/VG and VG mixtures with BA. Both VG and BA are sources of benzene. Enhanced emissions, however, are mostly noticeable when BA is mixed with PG and not VG.

Volatile organic compounds (VOCs) from diffuse degassing areas: Interstitial soil gases as message bearers from deep hydrothermal reservoirs

The chemical composition of volatile organic compounds (VOCs) in interstitial soil gases from hydrothermal areas is commonly shaped by both deep hydrothermal conditions (e.g., temperature, redox, sulfur fugacity) and shallow secondary processes occurring near the soil-atmosphere interface. Caldara di Manziana and Solfatara di Nepi, i.e., two hydrothermal systems characterized by diverse physicochemical conditions located in the Sabatini Volcanic District and Vicano-Cimino Volcanic District, respectively (Central Italy), were investigated to evaluate the capability of VOCs in soil gases to preserve information from the respective feeding deep fluid reservoirs. Hierarchical cluster analyses and robust principal component analyses allowed recognition of distinct groups of chemical parameters of soil gases collected from the two study areas. The compositional dissimilarities from the free-gas discharges were indeed reflected by the chemical features of soil gases collected from each site, despite the occurrence of shallow processes, e.g., air mixing and microbial degradation processes, affecting VOCs. Four distinct groups of VOCs were recognized suggesting similar sources and/or geochemical behaviors, as follows: (i) S-bearing compounds, whose abundance (in particular that of thiophenes) was strictly dependent on the sulfur fugacity in the feeding system; (ii) C4,5,7+ alkanes, n-hexane, cyclics and alkylated aromatics, related to relatively low-temperature conditions at the gas source; (iii) C2,3 alkanes, benzene, benzaldehyde and phenol, i.e., stable compounds and thermal degradation products; and (iv) aliphatic O-bearing compounds, largely influenced by shallow processes within the soil. However, they maintain a chemical speciation that preserves a signature derived from the supplying deep-fluids, with aldehydes and ketones becoming more enriched after intense interaction of the hypogenic fluids with shallow aquifers. Accordingly, the empirical results of this study suggest that the chemical composition of VOCs in soil gases from hydrothermal areas provides insights into both deep source conditions and fluid circulation dynamics, identifying VOCs as promising geochemical tracers for geothermal exploration.

Effects of different inhibitors on emission characteristics, environmental impact and health risk of volatile organic compounds from asphalt binder

Volatile organic compounds (VOCs) of asphalt will cause adverse environmental impact and workers’ health risk, inhibitors can be used to reduce the emission of VOCs from asphalt. Three inhibitors, including activated carbon (AC), expanded graphite (EG) and hydrotalcite (MA), were used to modified asphalt in this work. The effects of inhibitors on the VOCs emission characteristics of asphalt were investigated at multiple levels of VOCs total concentration, groups distribution and components characteristics. 101 asphalt VOCs components were detected, among which alkane accounted for more than 50% of the total concentration, followed by aldehyde and benzene. AC with the largest specific surface area and pore capacity exhibited the best inhibitory effect on the emission of VOCs with total concentration inhibition rate of 45.58%, followed by MA, while excessive MA would have adverse effect. Over 90% of VOCs components emissions had been suppressed by AC and EG. And inhibitors had the best inhibitory effect on the emission of olefin and aldehyde in VOCs, followed by ketone, but had the worst inhibitory effect on alkane, which was due to the weak interactions between non-polar alkane and polar hydroxyl on the surface of inhibitors. Furthermore, the effects of different inhibitors on the environmental impact and health risk of VOCs from asphalt were also systematically studied. The highest total inhibition rate of OFP and SOAP from asphalt VOCs by AC was only 58.3% and 21.7%, which was ascribed to the limited suppression on OFP and SOAP generated by alkane and benzene. Meanwhile, the non-carcinogenic risk from asphalt VOCs was mainly caused by acrolein with a contribution rate of 80.0%, AC and EG can completely inhibit the emission of acrolein in asphalt VOCs, while MA showed the poor performance. The contribution rate of acetaldehyde to the carcinogenic risk of asphalt VOCs reached 93.7%, while inhibitors had limited inhibitory effects on its emissions. This study contributes to a deeper understanding of the correlation mechanism between inhibitors, emission reduction characteristics of asphalt VOCs and environmental-health benefits, which could provide theoretical support for the design of bituminous material with low environmental-health load.

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.

Suppressive Effects of Volatile Compounds from Bacillus spp. on Magnaporthe oryzae Triticum (MoT) Pathotype, Causal Agent of Wheat Blast.

The Magnaporthe oryzae Triticum (MoT) pathotype is the causal agent of wheat blast, which has caused significant economic losses and threatens wheat production in South America, Asia, and Africa. Three bacterial strains from rice and wheat seeds (B. subtilis BTS-3, B. velezensis BTS-4, and B. velezensis BTLK6A) were used to explore the antifungal effects of volatile organic compounds (VOCs) of Bacillus spp. as a potential biocontrol mechanism against MoT. All bacterial treatments significantly inhibited both the mycelial growth and sporulation of MoT in vitro. We found that this inhibition was caused by Bacillus VOCs in a dose-dependent manner. In addition, biocontrol assays using detached wheat leaves infected with MoT showed reduced leaf lesions and sporulation compared to the untreated control. VOCs from B. velezensis BTS-4 alone or a consortium (mixture of B. subtilis BTS-3, B. velezensis BTS-4, and B. velezensis BTLK6A) of treatments consistently suppressed MoT in vitro and in vivo. Compared to the untreated control, VOCs from BTS-4 and the Bacillus consortium reduced MoT lesions in vivo by 85% and 81.25%, respectively. A total of thirty-nine VOCs (from nine different VOC groups) from four Bacillus treatments were identified by gas chromatography-mass spectrometry (GC-MS), of which 11 were produced in all Bacillus treatments. Alcohols, fatty acids, ketones, aldehydes, and S-containing compounds were detected in all four bacterial treatments. In vitro assays using pure VOCs revealed that hexanoic acid, 2-methylbutanoic acid, and phenylethyl alcohol are potential VOCs emitted by Bacillus spp. that are suppressive for MoT. The minimum inhibitory concentrations for MoT sporulation were 250 mM for phenylethyl alcohol and 500 mM for 2-methylbutanoic acid and hexanoic acid. Therefore, our results indicate that VOCs from Bacillus spp. are effective compounds to suppress the growth and sporulation of MoT. Understanding the MoT sporulation reduction mechanisms exerted by Bacillus VOCs may provide novel options to manage the further spread of wheat blast by spores.

Thermal processing-induced changes in volatilome and metabolome of Brussels sprouts: focus on glucosinolate metabolism

This study aimed to investigate the influence of different thermal treatment methods (boiling, steaming) on the metabolome and volatilome of Brussels sprouts. Targeted, quantitative analysis of primary metabolites (amino acids and sugars), glucosinolates as well as untargeted analysis of volatile organic compounds (VOCs) were performed. The composition of primary metabolites was affected only by boiling, where the loss of nutrients was observed. Glucosinolate content increased after cooking, which can be explained by the loosening of the plant tissues and its better extractability. Most marked changes were noticed in the volatilome. Among the degradation products of glucosinolates, isothiocyanates were the main chemical group in the raw and boiled vegetable. In contrast, steaming favored the formation of nitriles. Another dominant group of VOCs were aldehydes, which were the most abundant in raw Brussels sprouts and their level significantly decreased after thermal treatment. It is well known that isothiocyanates are substances with widely proven bioactive properties. Therefore, their formation in the glucosinolate degradation process is favorable. Based on the obtained results, it was concluded that boiling seems to be the most beneficial form of Brussels sprouts’ processing.

Characteristics and source apportionment of ambient volatile organic compounds and ozone generation sensitivity in urban Jiaozuo, China

In recent years, many cities have taken measures to reduce volatile organic compounds (VOCs), an important precursor of ozone (O3), to alleviate O3 pollution in China. 116 VOC species were measured by online and offline methods in the urban area of Jiaozuo from May to October in 2021 to analyze the compositional characteristics. VOC sources were analyzed by a positive matrix factorization (PMF) model, and the sensitivity of ozone generation was determined by ozone isopleth plotting research (OZIPR) simulation. The results showed that the average volume concentration of total VOCs was 30.54 ppbv and showed a bimodal feature due to the rush-hour traffic in the morning and at nightfall. The most dominant VOC groups were oxygenated VOCs (OVOCs, 29.3%) and alkanes (26.7%), and the most abundant VOC species were acetone and acetylene. However, based on the maximum incremental reactivity (MIR) method, the major VOC groups in terms of ozone formation potential (OFP) contribution were OVOCs (68.09 µg/m3, 31.5%), aromatics (62.90 µg/m3, 29.1%) and alkene/alkynes (54.90 µg/m3, 25.4%). This indicates that the control of OVOCs, aromatics and alkene/alkynes should take priority. Five sources of VOCs were quantified by PMF, including fixed sources of fossil fuel combustion (27.8%), industrial processes (25.9%), vehicle exhaust (19.7%), natural and secondary formation (13.9%) and solvent usage (12.7%). The empirical kinetic modeling approach (EKMA) curve obtained by OZIPR on O3 exceedance days indicated that the O3 sensitivity varied in different months. The results provide theoretical support for O3 pollution prevention and control in Jiaozuo.

Sensitivity analysis of volatile organic compounds to PM2.5 concentrations in a representative industrial city of Korea

This study aims to analyze the sensitivity of volatile organic compounds (VOCs) to ambient concentrations of fine particles (PM2.5) in the representative industrial city of Ulsan, Korea. For the calculation of sensitivity coefficients between VOCs and PM2.5 (SVOCs-PM2.5), PM2.5 data were obtained from an air quality monitoring station, and their corresponding 6-h average concentrations of VOCs (alkanes, alkenes, aromatics, and total VOCs) were measured at the Yeongnam intensive air monitoring station. The air monitoring period was divided into the warm-hot season (May–October 2020) and the cold season (November 2020–January 2021). The sensitivity coefficients in the low pollution period of PM2.5 (5 < PM2.5 ≤ 15 μg/m3) were higher and much higher than those in the medium pollution period (15 < PM2.5 ≤ 35 μg/m3) and high pollution period (35 < PM2.5 ≤ 50 μg/m3), respectively. This result indicates that the change ratios of PM2.5 concentrations to the background (PM2.5 ≤ 5 μg/m3) per unit concentration change of VOCs (particularly alkenes) in the high PM2.5 pollution period were much higher than those in the low pollution period. This also indicates that PM2.5 concentrations above 35 μg/m3 were more easily affected by the unit concentration change of VOCs (particularly alkenes) than those below 15 μg/m3. The average sensitivity coefficients during the cold season increased in a range of 23–125% as compared to those during the warm-hot season, except the alkenes-PM2.5 sensitivity with a decrease of 7%. It means that the impact of VOCs (except alkenes) on PM2.5 concentrations was relatively low in the cold season. However, in the cold season, the alkenes might contribute more to PM2.5 formation, particularly over the high pollution period, having PM2.5 > 35 μg/m3, than other VOC groups. The result of this study can be a basis for establishing PM2.5 management plans in industrial cities with large VOC emissions.

Characterizing sources and ozone formations of summertime volatile organic compounds observed in a medium-sized city in Yangtze River Delta region

Volatile organic compounds (VOCs) emitted from various sources into atmosphere could cause serious O3 pollution in urban areas. Although characterizations of ambient VOCs have been extensively studied in megacities, they are scarcely investigated in medium/small-sized cities, which could present different pollution characterizations due to the factors like emission sources and populations. Herein, field campaigns were conducted concurrently at six sites in a medium-sized city of Yangtze River Delta region to determine ambient levels, O3 formations and source contributions of summertime VOCs. During the observation period, the total VOC (TVOCs) mixing ratios ranged from 27.10 ± 3.35 to 39.09 ± 10.84 ppb at six sites. The ozone formation potential (OFP) results showed that alkenes, aromatics and oxygenated VOCs (OVOCs) were dominant contributors, together sharing 81.4% of total calculated OFPs. Ethene ranked the largest OFP contributor at all six sites. A high VOC site, KC, was selected as a case to detailed analyze diurnal variations of VOCs and its relationship with O3. Consequently, diurnal patterns varied with VOC groups, and TVOC concentrations were lowest during strong photochemical period (15:00–18:00 p.m.), opposite to the O3 peak. VOCs/NOx ratios and observation-based model (OBM) analysis revealed that O3 formation sensitivity was primarily in transition regime in summertime and that the reduction of VOCs rather than NOX would be more efficient to suppress O3 peak at KC during pollution episode. Additionally, source apportionment conducted with positive matrix factorization (PMF) indicated that industrial emission (29.2%–51.7%) and gasoline exhaust (22.4%–41.1%) were major sources for VOCs at all six sites, and that VOCs from industrial emissions and gasoline exhaust were the key precursors for ozone formation. Our results shed light on the importance of alkenes, aromatics and OVOCs in forming O3 and propose that preferentially reducing VOCs especially those from industrial emission and gasoline exhaust would benefit alleviating O3 pollution.

Nanofibers as optical sensors for model VOCs dispersed in aqueous phase

AbstractNanofibers mats, prepared from poly(vinyl chloride) (PVC) containing dispersed dye Nile red (NR) were applied in a proof of concept study as optical sensors for Volatile Organic Compounds (VOCs) dispersed in an aqueous phase. Benefiting from the solubility of the dye, and in some cases, also of the polymer in model solvents belonging to the group of VOCs, an increase of emission was observed for increasing solvent concentration in the sample. The optical signal formation was observed regardless if only the dye or both dye and PVC were soluble in the tested solvent. In both cases, high sensitivity emission increases for increasing VOCs present in the aqueous phase were observed within the range of concentration of model analytes: from 200 ppm of m‐xylene or from 300 ppm of styrene, to up to ca 1500 ppm. The obtained higher detection limit was lower compared to films of PVC containing the dye due to the lower availability of the material to be dissolved by analyte – solvent. The large surface area of nanofibers was useful in the detection, leading to higher signal changes compared to films.

Volatile responses of dwarf birch to mimicked insect herbivory and experimental warming at two elevations in Greenlandic tundra.

Plants release a complex blend of volatile organic compounds (VOCs) in response to stressors. VOC emissions vary between contrasting environments and increase with insect herbivory and rising temperatures. However, the joint effects of herbivory and warming on plant VOC emissions are understudied, particularly in high latitudes, which are warming fast and facing increasing herbivore pressure. We assessed the individual and combined effects of chemically mimicked insect herbivory, warming, and elevation on dwarf birch (Betula glandulosa) VOC emissions in high-latitude tundra ecosystems in Narsarsuaq, South Greenland. We hypothesized that VOC emissions and compositions would respond synergistically to warming and herbivory, with the magnitude differing between elevations. Warming increased emissions of green leaf volatiles (GLVs) and isoprene. Herbivory increased the homoterpene, (E)-4,8-dimethyl-1,3,7-nonatriene, emissions, and the response was stronger at high elevation. Warming and herbivory had synergistic effects on GLV emissions. Dwarf birch emitted VOCs at similar rates at both elevations, but the VOC blends differed between elevations. Several herbivory-associated VOC groups did not respond to herbivory. Harsher abiotic conditions at high elevations might not limit VOC emissions from dwarf birch, and high-elevation plants might be better at herbivory defense than assumed. The complexity of VOC responses to experimental warming, elevation, and herbivory are challenging our understanding and predictions of future VOC emissions from dwarf birch-dominated ecosystems.

Volatile organic compound emissions from typical industries: Implications for the importance of oxygenated volatile organic compounds

Industrial productions emit large reactive volatile organic compounds (VOCs) into atmosphere, affecting tropospheric atmospheric chemistry and human health. In this study, VOC samples of industrial process and solvent use were collected from typical industries. The mass concentrations of total VOC (TVOCs) were 34.10 ± 35.46 mg m−3 (mean ± 95% C.I.) measured in industrial process and 25.39 ± 16.88 mg m−3 in solvent use. Difference of VOC profiles between industrial process and solvent use was revealed. Much higher concentrations or percentages of halocarbons were emitted from industrial process, while more abundant alkanes were measured in solvent use. The relative proportions of B:T:E (benzene, toluene and ethylbenzene) were similar for these two industrial sources, but quite different from that of combustion sources. Different ratios of F/A (formaldehyde/acetaldehyde) and A/P (acetaldehyde/propionaldehyde) were found between industrial process and solvent use, suggesting that the ratios might be used as the references to distinguish these two industrial sources. The oxygenated VOCs (OVOCs) were the largest VOC group and ranked No.1 contributor of ozone formation potentials (OFPs) in these two sources. Our results provide the source profiles of industrial VOCs and emphasize the contribution of industrial OVOCs in ozone formations.

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

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

Characteristics and sources of ambient Volatile Organic Compounds (VOCs) at a regional background site, YRD region, China: Significant influence of solvent evaporation during hot months

Continuous measurement of 98 volatile organic compounds (VOCs) was conducted during 2017–2019 at a regional background site (Shanxi) located at northeast of Zhejiang Province, YRD region, China. The average concentration of total VOCs (TVOCs) was 25.4 ± 18.4 ppbv, and an increasing trend (+12.2 %) was observed. Alkanes were the most abundant VOC group among all seasons, accounting for 43.5 % of TVOCs. Oxygenated VOCs (OVOCs), aromatics, halides and alkenes contributed 15.9 %, 15.7 %, 11.7 % and 10.3 % of TVOCs concentration, respectively. Biogenic VOCs (BVOCs) and OVOCs showed distinguished diurnal cycle from primary anthropogenic VOCs. Photochemical reactivity analysis based on ozone formation potential (OFP) and OH loss rate (LOH) indicated that aromatics and alkenes were the most significant contributor, respectively. Toluene, xylene (m/p- and o-), ethene and propene were the largest contributor of annual OFP, with the mean OFP being 33.8 ± 44.3 μg·m−3, 31.9 ± 32.1 μg·m−3, 9.29 ± 11.4 μg·m−3, 22.1 ± 21.3 μg·m−3 and 12.8 ± 19.5 μg·m−3, respectively. Seven sources were identified with positive matrix factorization (PMF): petrochemical industry (13.8 %), biogenic emission (1.0 %), solvent usage-toluene (16.9 %), vehicular exhaust (43.8 %), Integrated circuits industry (3.8 %), solvent usage-C8 aromatics (10.9 %), and gasoline evaporation (9.8 %). Vehicular exhaust was the most significant source (43.8 %) during the whole measurement period. Solvent usage, petrochemical industry, and gasoline evaporation showed high temperature dependency. The integrated contribution of solvent usage and industrial processes were higher than vehicular exhaust during hot months. These sources also have higher chemical reactivities and can contribute more on O3 formation. Our results are helpful on determining the control strategies aiming at alleviating O3 pollution.

Determination of volatile organic compounds: allowable storage times for sorption tubes after sampling

Introduction. Monitoring and control of priority chemicals presented in the emissions in cities of Lipetsk, Omsk, Cherepovets, Novokuznetsk, participating in «The Clean Air» Federal project, require frequent sampling of air samples, their transportation and storage prior to analysis. Since most samples are not analyzed immediately after sampling, correct quantitative results can only be obtained if there is verified data on the long-term stability of volatile organic compounds (VOCs) collected on sorption tubes. The purpose of this work is to obtain up-to-date, experimentally substantiated data on the stability of various VOCs during storage of exposed sorption tubes in laboratory conditions. Materials and methods. Several groups of VOCs have been selected as the most common air pollutants. VOC stability tests during storage up to 5 months were carried out on model samples using sorption tubes filled with Tenax TA sorbent. The VOC content was determined by thermal desorption (TD) and gas chromatographic analysis using mass spectrometric detection (GC-MS). Results. When stored under laboratory conditions at a temperature of (20 ± 5)°C and humidity in the range of 33-65% in hermetically sealed containers or a glass desiccator, there was shown the stability of 28 VOCs, taken on tubes filled with Tenax TA sorbent: trichloromethane, carbon tetrachloride, trichlorethylene, tetrachlorethylene, benzene, o-xylene, the sum of isomers of m-xylene and p-xylene, ethylbenzene, n-octane, toluene, n-butanol, n-heptane, 1,2-dichloroethane, n-hexane, dichloromethane, ethyl acetate, n-butyl acetate, chlorobenzene, isopropylbenzene, α-pinene, n-propylbenzene, α-methylstyrene, 2-butoxyethanol, styrene up to 5 months; for 5 VOCs: phenol, pentanal (valeric aldehyde), hexanal (caproic aldehyde), n-nonane and n-decane - no more than 4 weeks. Limitations. The stability of the investigated VOCs was not studied at low (less than 15 °C) and high (more than 25 °C) temperatures, as well as high humidity (more than 65 %). Conclusion. The results obtained allow planning the frequency and period of air sampling and the time of their storage in the form of exposed tubes before transfer to the laboratory, as well as the time of preparation and storage, taking into account the throughput of the equipment during their analysis in the laboratory.