Reactivity-based industrial volatile organic compounds emission inventory and its implications for ozone control strategies in China

2017 ◽  
Vol 162 ◽  
pp. 115-126 ◽  
Author(s):  
Xiaoming Liang ◽  
Xiaofang Chen ◽  
Jiani Zhang ◽  
Tianli Shi ◽  
Xibo Sun ◽  
...  
Agronomy ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 956
Author(s):  
Jong-Kwon Im ◽  
Yong-Chul Cho ◽  
Hye-Ran Noh ◽  
Soon-Ju Yu

Volatile organic compounds (VOCs), with negative impacts on the aquatic ecosystem, are increasingly released into the environment by anthropogenic activities. Water samples were collected from five areas of the Han River Watershed (HRW) tributaries, South Korea, to detect 11 VOCs, which were classified as halogenated aliphatic hydrocarbons (HAHs) and aromatic hydrocarbons (AHs). Among the 11 VOCs, 1,1-dichloroethylene, 1,1,1-trichloroethane, and vinyl chloride were undetected. The highest concentration compounds were chloroform (0.0596 ± 0.1312 µg/L), trichloroethylene (0.0253 ± 0.0781 µg/L), and toluene (0.0054 ± 0.0139 µg/L). The mean concentration (0.0234 µg/L) and detection frequency (37.0%) of HAHs were higher than those of AHs (0.0036 µg/L, 21.0%, respectively). The Imjin Hantan River area exhibited the highest mean concentration (0.2432 µg/L) and detection frequency (22.9%), because it is located near industrial complexes, thus, highlighting their role as important VOC sources. However, the detected VOCs had lower concentrations than those permitted by the EU, WHO, USA, and South Korea drinking water guidelines. Ecological risks associated with the VOCs were estimated by risk quotient (RQ); consequently, the predicted no-effect concentration was 0.0029 mg/L, and the toluene and styrene RQ values were >1 and >0.5, respectively. The findings may facilitate policymakers in designing pollution control strategies.


2011 ◽  
Vol 8 (1) ◽  
pp. 91 ◽  
Author(s):  
Cécile Gaimoz ◽  
Stéphane Sauvage ◽  
Valérie Gros ◽  
Frank Herrmann ◽  
Jonathan Williams ◽  
...  

Environmental context Volatile organic compounds are key compounds in atmospheric chemistry as precursors of ozone and secondary organic aerosols. To determine their impact at a megacity scale, a first important step is to characterise their sources. We present an estimate of volatile organic compound sources in Paris based on a combination of measurements and model results. The data suggest that the current emission inventory strongly overestimates the volatile organic compounds emitted from solvent industries, and thus needs to be corrected. Abstract A positive matrix factorisation model has been used for the determination of volatile organic compound (VOC) source contributions in Paris during an intensive campaign (May–June 2007). The major sources were traffic-related emissions (vehicle exhaust, 22% of the total mixing ratio of the measured VOCs, and fuel evaporation, 17%), with the remaining emissions from remote industrial sources (35%), natural gas and background (13%), local sources (7%), biogenic and fuel evaporation (5%) and wood-burning (2%). It was noted that the remote industrial contribution was highly dependent on the air-mass origin. During the period of oceanic influences (when only local and regional pollution was observed), this source made a relatively low contribution (<15%), whereas the source contribution linked to traffic was high (54%). During the period of continental influences (when additional continental pollution was observed), remote industrial sources played a dominant role, contributing up to 50% of measured VOCs. Finally, the positive matrix factorisation results obtained during the oceanic air mass-influenced period were compared with the local emission inventory. This comparison suggests that the VOC emission from solvent industries might be overestimated in the inventory, consistent with findings in other European cities.


2020 ◽  
Vol 727 ◽  
pp. 138654 ◽  
Author(s):  
Hamid Rajabi ◽  
Mojgan Hadi Mosleh ◽  
Parthasarathi Mandal ◽  
Amanda Lea-Langton ◽  
Majid Sedighi

2017 ◽  
Vol 17 (12) ◽  
pp. 7733-7756 ◽  
Author(s):  
Yu Zhao ◽  
Pan Mao ◽  
Yaduan Zhou ◽  
Yang Yang ◽  
Jie Zhang ◽  
...  

Abstract. Non-methane volatile organic compounds (NMVOCs) are the key precursors of ozone (O3) and secondary organic aerosol (SOA) formation. Accurate estimation of their emissions plays a crucial role in air quality simulation and policy making. We developed a high-resolution anthropogenic NMVOC emission inventory for Jiangsu in eastern China from 2005 to 2014, based on detailed information of individual local sources and field measurements of source profiles of the chemical industry. A total of 56 NMVOCs samples were collected in nine chemical plants and were then analyzed with a gas chromatography – mass spectrometry system (GC-MS). Source profiles of stack emissions from synthetic rubber, acetate fiber, polyether, vinyl acetate and ethylene production, and those of fugitive emissions from ethylene, butanol and octanol, propylene epoxide, polyethylene and glycol production were obtained. Various manufacturing technologies and raw materials led to discrepancies in source profiles between our domestic field tests and foreign results for synthetic rubber and ethylene production. The provincial NMVOC emissions were calculated to increase from 1774 Gg in 2005 to 2507 Gg in 2014, and relatively large emission densities were found in cities along the Yangtze River with developed economies and industries. The estimates were larger than those from most other available inventories, due mainly to the complete inclusion of emission sources and to the elevated activity levels from plant-by-plant investigation in this work. Industrial processes and solvent use were the largest contributing sectors, and their emissions were estimated to increase, respectively, from 461 to 958 and from 38 to 966 Gg. Alkanes, aromatics and oxygenated VOCs (OVOCs) were the most important species, accounting for 25.9–29.9, 20.8–23.2 and 18.2–21.0 % to annual total emissions, respectively. Quantified with a Monte Carlo simulation, the uncertainties of annual NMVOC emissions vary slightly through the years, and the result for 2014 was −41 to +93 %, expressed as 95 % confidence intervals (CI). Reduced uncertainty was achieved compared to previous national and regional inventories, attributed partly to the detailed classification of emission sources and to the use of information at plant level in this work. Discrepancies in emission estimation were explored for the chemical and refinery sectors with various data sources and methods. Compared with the Multi-resolution Emission Inventory for China (MEIC), the spatial distribution of emissions in this work were more influenced by the locations of large point sources, and smaller emissions were found in urban area for developed cities in southern Jiangsu. In addition, discrepancies were found between this work and MEIC in the speciation of NMVOC emissions under the atmospheric chemistry mechanisms CB05 and SAPRC99. The difference in species OLE1 resulted mainly from the updated source profile of building paint use and the differences in other species from the varied sector contributions to emissions in the two inventories. The Community Multi-scale Air Quality (CMAQ) model simulation was applied to evaluate the two inventories, and better performance (indicated by daily 1 h maximum O3 concentrations in Nanjing) were found for January, April and October 2012 when the provincial inventory was used.


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