Screening the emission sources of volatile organic compounds (VOCs) in China by multi-effects evaluation

Author(s):  
He Niu ◽  
Ziwei Mo ◽  
Min Shao ◽  
Sihua Lu ◽  
Shaodong Xie
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.


2016 ◽  
Author(s):  
A. Baudic ◽  
V. Gros ◽  
S. Sauvage ◽  
N. Locoge ◽  
O. Sanchez ◽  
...  

Abstract. Within the framework of air quality studies at the megacity scale, highly time-resolved volatile organic compounds (C2–C8) measurements were performed in downtown Paris (urban background sites) from January to November 2010. This unique dataset included non-methane hydrocarbons (NMHCs) and aromatic/oxygenated species (OVOCs) measured by a GC-FID (Gas Chromatograph with a Flame Ionization Detector) and a PTR-MS (Proton Transfer Reaction – Mass Spectrometer), respectively. The current study presents the seasonal variability of atmospheric VOCs being monitored in the French megacity and their various associated emission sources. Clear seasonal and diurnal patterns differed from one VOC to another as the result of their different origins and the influence of environmental parameters (solar radiation, temperature). Source Apportionment (SA) was comprehensively conducted using a multivariate mathematical receptor modeling. The United States Environmental Protection Agency's Positive Matrix Factorization tool (US EPA, PMF) was used to apportion and quantify ambient VOC concentrations into six different sources. The modeled source profiles were identified from near-field observations (measurements from three distinct emission sources: inside a highway tunnel, at a fireplace and from a domestic gas flue, with hence a specific focus on road-traffic, wood burning activities and natural gas emissions) and hydrocarbon profiles reported in the literature. The reconstructed VOC sources were cross-validated using independent tracers such as inorganic gases (NO, NO2, CO), black carbon (BC) and meteorological data (temperature). The largest contributors to the predicted VOC concentrations were traffic-related activities (including motor vehicle exhaust, 15 % of the total mass on the annual average, and gasoline evaporation, 10 %), with the remaining emissions from natural gas and background (23 %), solvents use (20 %), wood burning (18 %) and a biogenic source (15 %). An important finding of this work is the significant contribution from wood burning, especially in winter, where it could represent up to ~ 50 % of the total mass of VOCs. Biogenic emissions also surprisingly contributed up to ~ 30 % in summer (due to the dominating weight of OVOCs in this source). Finally, the mixed natural gas and background source exhibited a high contribution in spring (35 %, when continental air influences were observed) and in autumn (23 %, for home heating consumption).


2015 ◽  
Vol 115 ◽  
pp. 153-162 ◽  
Author(s):  
Qiusheng He ◽  
Yulong Yan ◽  
Hongyan Li ◽  
Yiqiang Zhang ◽  
Laiguo Chen ◽  
...  

2017 ◽  
Author(s):  
Yu Zhao ◽  
Pan Mao ◽  
Yaduan Zhou ◽  
Yang Yang ◽  
Jie Zhang ◽  
...  

Abstract. Non-methane volatile organic compounds (NMVOC) are the key precursors of ozone (O3) and secondary organic aerosol (SOA) formation. Accurate estimation in their emissions plays a crucial role in air quality simulation and policy making. We developed a high-resolution anthropogenic NMVOCs emission inventory for Jiangsu in eastern China from 2005 to 2014, based on detailed information of individual local sources and the field measurements on source profiles of chemical industry. Totally 56 NMVOCs samples were collected in 9 chemical plants, and 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 lead 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 economy and industry. 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 NMVOCs emissions vary slightly from years, and the result for 2014 was −41 % ~ +93 %, expressed as 95 % confidence intervals (CI). Reduced uncertainty was achieved compared to previous national and regional inventories, attributed mainly 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 chemical and refinery sector with various data sources and methods. Compared with 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 region for developed cities in southern Jiangsu. Besides, clear discrepancies were found between this work and MEIC in the speciation of NMVOC emissions under the atmospheric chemistry mechanisms CB05 and SAPRC99. The difference of species OLE1 resulted mainly from the updated source profile of building paint use, and the differences of other species from the varied sector contributions to emissions of the two inventories. CMAQ simulation was applied to evaluate the two inventories, and better performance (indicated by daily 1h-max O3 concentrations in Nanjing city) was found for January, April and October 2012 when the provincial inventory was used.


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