Search Results (6)

In this study, online ambient volatile organic compounds (VOCs) were collected at an urban site of Zhengzhou in Central China during February 2018. The VOCs characteristics, source contributions and the Chinese New Year (CNY) effects have been investigated. During the sampling period, three haze periods have been identified, with the corresponding VOCs concentrations of (92 ± 45) ppbv, (62 ± 18) ppbv and (83 ± 34) ppbv; in contrast, the concentration during non-haze days was found to be (57 ± 27) ppbv. In addition, the festival effects of the CNY were investigated, and the concentration of particulate matter precursor decreased significantly. Meanwhile, firework-displaying events were identified, as the emission intensity had been greatly changed. Both potential source contribution function (PSCF) and the concentration weighted trajectory (CWT) models results indicated that short-distance transportation was the main influencing factor of the local VOCs pollution, especially by transport from the northeast. Source contribution results by the positive matrix factorization (PMF) model showed that vehicle exhaust (24%), liquid petroleum gas and natural gas (LPG/NG, 23%), coal combustion (21%), industrial processes (16%) and solvent usages (16%) were the major sources of ambient VOCs. Although industry and solvents have low contribution to the total VOCs, their secondary organic aerosol (SOA) contribution were found to be relatively high, especially in haze-1 and haze-3 periods. The haze-2 period had the lowest secondary organic aerosol potential (SOAp) during the sampling period; this is mainly caused by the reduction of industrial and solvent emissions due to CNY. Full article

Volatile organic compounds (VOCs) are the main precursors of pollution from ground ozone (O₃) and PM_2.5, which cause the deterioration of urban air quality. The emissions of VOCs from industrialized areas are significant and their characteristics are complex, which nowadays contribute significantly to the challenges of investigating the emission inventory. Taking a typical industrialized area in Tianjin as a case study, the anthropogenic VOCs emission inventory for 2020 was established in this study by using the activity data from a large-scale survey and the latest emission factors. The impact of VOCs on the environment was analyzed from the perspective of the combined control of PM_2.5 and O₃. The results showed that the total emission of VOCs in 2020 was about 1.68 Gg, mainly from industrial processes and mobile sources, which accounted for 38.4% and 36.5% of the total emissions, respectively. The top 10 emitted VOCs were toluene, acetone, ethylbenzene, m/p-xylene, i-pentane, n-hexane, formaldehyde, benzene, ethyl acetate and ethylene. The dominant species of O₃ formation potential (OFP) were almost all aromatic hydrocarbons and alkenes, with m/p-xylene contributing the most to the OFP emissions (8.90%). The top 10 secondary organic aerosols formation potential (SOAP) emission species were aromatic hydrocarbons and long-chain alkanes, and the largest emission came from toluene (39.9%). An analysis of an ADMS diffusion model showed that VOCs emitted from traffic-heavy main roads and industrialized central areas had the greatest impact on the air quality in the surrounding areas. The VOCs concentration was higher in winter due to unfavorable meteorological conditions. Our research updated the VOC inventory of industrialized areas and evaluated VOCs species reactivity and their impact on ambient air quality. Full article

Volatile organic compounds (VOCs) emitted by plant foliage play an important role in ozone (O₃) and secondary organic aerosol (SOA) formation. Their emissions can be influenced by the leaf age. We explored the VOCs emissions and their effects on the formation of O₃ and SOA from plant foliage in different ages. VOCs emissions from the young, mature, and senescent leaves of Ginkgo biloba, Ligustrum lucidum, and Forsythia suspensa were measured using the dynamic enclosure system and the TD–GC–MS technique. Based on the emission rates of quantified compounds, their potential to form O₃ and SOA was estimated. Results showed that there were significant differences in the VOCs emission rate and their composition among leaves in different ages. The emission rate of the total VOCs by young leaves was the highest, while the lowest by senescent leaves. Monoterpenes were the dominant VOCs category, and isoprene emission had the lowest contribution for the leaves at each age. With increasing leaf age, the proportion of monoterpenes emission increased, and the proportion of sesquiterpenes decreased. The variations of isoprene and other VOCs were different. The potentials of total VOCs, isoprene, monoterpenes, sesquiterpenes, and other VOCs to form O₃ (OFP) and SOA (SOAP) varied significantly among leaves at different ages. The total OFP and SOAP were the highest by young leaves, while the lowest by senescent leaves. With increasing leaf age, the contribution of monoterpenes to OFP and SOAP also increased, while that of sesquiterpenes decreased. Our study will provide support for the more accurate parameterization of the emission model and help to understand the VOCs emissions and study the precise prevention and control of complex air pollution at different times. Full article

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

In this study, 56 volatile organic compounds species (VOCs) and other pollutants (NO, NO₂, SO₂, O₃, CO and PM_2.5) were measured in the northern suburbs of Nanjing from September 2014 to August 2015. The total volatile organic compound (TVOC) concentrations were higher in the autumn (40.6 ± 23.8 ppbv) and winter (41.1 ± 21.7 ppbv) and alkanes were the most abundant species among the VOCs (18.4 ± 10.0 ppbv). According to the positive matrix factorization (PMF) model, the VOCs were found to be from seven sources in the northern suburbs of Nanjing, including liquefied petroleum gas (LPG) sources, gasoline vehicle emissions, iron and steel industry sources, industrial refining coke sources, solvent sources and petrochemical industry sources. One of the sources was influenced by seasonal variations: it was a diesel vehicle emission source in the spring, while it was a coal combustion source in the winter. According to the conditional probability function (CPF) method, it was found that the main contribution areas of each source were located in the easterly direction (mainly residential areas, industrial areas, major traffic routes, etc.). There were also seasonal differences in concentration, ozone formation potential (OFP), OH radical loss rate (L^OH) and secondary organic aerosols potential (SOAP) for each source due to the high volatility of the summer and autumn temperatures, while combustion increases in the winter. Finally, the time series of O₃ and OFP was compared to that PM_2.5 and SOAP and then they were combined with the wind rose figure. It was found that O₃ corresponded poorly to the OFP, while PM_2.5 corresponded well to the SOAP. The reason for this was that the O₃ generation was influenced by several factors (NO_x concentration, solar radiation and non-local transport), among which the influence of non-local transport could not be ignored. Full article

Non-methane hydrocarbons (NMHCs) from four sampling sites in Lanzhou, a petrochemical industrialized city in northwest China, was sampled by stainless steel canisters and measured by gas chromatography–mass selective detection/flame ionization detection (GC–MSD/FID) in May and June of 2017. Based on these results, the contributions of NMHCs to the ozone (O₃) and secondary organic aerosols (SOA), differences in tracer ratios, and source apportionment by principal component analysis (PCA) were analyzed. The results showed that the total NMHCs concentration in Lanzhou was 48.4 ± 48.3 ppbv (parts per billion by volume) during the observation and it was higher in May (78.6 ppbv) than in June (37.8 ppbv); the highest NMHCs concentration was observed in industrial areas. Alkanes were the dominant group at all sites in Lanzhou and account for more than 60% of the NMHCs, while isopentane, n-butane n-pentane, propane and ethane were the major compounds. Additionally, the NMHCs in Lanzhou have made great contributions to O₃ and SOA generation and the S1 site of the industrial area contributed the most to both of them. Propene, toluene, ethylbenzene and n-pentane were found to be more reactive with relatively high contributions to ozone formation. Aromatics and high carbon alkanes were major contributors to SOA formation potential (SOAp) (i.e., toluene, m,p-xylene, dodecane, undecane, n-tanane, benzene and ethylbenzene) in Lanzhou. Based on the specific volatile organic compounds (VOCs) ratio method and the PCA modem, the observation sites in Lanzhou were greatly affected by the surrounding industrial areas. The sources consisted of petrochemical industry, vehicle emissions, solvent usage and combustion sources, which contributed to 33.9%, 31.6%, 19.2% and 7.9% of the total monitored NMHCs, respectively. From different sites, though the influence of regional transport was not very significant on the whole, it also affected the NMHCs of nonindustrial areas based on the ratio of xylene to ethyl-benzene (X/E), especially the S4 site; vehicle emission was less important compared to sources from petrochemical industries in S1, as characterized by relatively higher toluene to benzene (T/B) ratios. However, vehicle emission has significant influence on NMHCs in S4. Overall, local emissions are the main source of NMHCs in Lanzhou and the petrochemical industry has a great influence on the distribution of NMHCs in the whole region. Full article