A newly integrated dataset of volatile organic compounds (VOCs) source profiles and implications for the future development of VOCs profiles in China

Author(s):  
Qing'e Sha ◽  
Manni Zhu ◽  
Hewen Huang ◽  
Yuzheng Wang ◽  
Zhijiong Huang ◽  
...  
2018 ◽  
Vol 18 (23) ◽  
pp. 17637-17654 ◽  
Author(s):  
Quanyang Lu ◽  
Yunliang Zhao ◽  
Allen L. Robinson

Abstract. Emissions from mobile sources are important contributors to both primary and secondary organic aerosols (POA and SOA) in urban environments. We compiled recently published data to create comprehensive model-ready organic emission profiles for on- and off-road gasoline, gas-turbine, and diesel engines. The profiles span the entire volatility range, including volatile organic compounds (VOCs, effective saturation concentration C*=107–1011 µg m−3), intermediate-volatile organic compounds (IVOCs, C*=103–106 µg m−3), semi-volatile organic compounds (SVOCs, C*=1–102 µg m−3), low-volatile organic compounds (LVOCs, C*≤0.1 µg m−3) and non-volatile organic compounds (NVOCs). Although our profiles are comprehensive, this paper focuses on the IVOC and SVOC fractions to improve predictions of SOA formation. Organic emissions from all three source categories feature tri-modal volatility distributions (“by-product” mode, “fuel” mode, and “lubricant oil” mode). Despite wide variations in emission factors for total organics, the mass fractions of IVOCs and SVOCs are relatively consistent across sources using the same fuel type, for example, contributing 4.5 % (2.4 %–9.6 % as 10th to 90th percentiles) and 1.1 % (0.4 %–3.6 %) for a diverse fleet of light duty gasoline vehicles tested over the cold-start unified cycle, respectively. This consistency indicates that a limited number of profiles are needed to construct emissions inventories. We define five distinct profiles: (i) cold-start and off-road gasoline, (ii) hot-operation gasoline, (iii) gas-turbine, (iv) traditional diesel and (v) diesel-particulate-filter equipped diesel. These profiles are designed to be directly implemented into chemical transport models and inventories. We compare emissions to unburned fuel; gasoline and gas-turbine emissions are enriched in IVOCs relative to unburned fuel. The new profiles predict that IVOCs and SVOC vapour will contribute significantly to SOA production. We compare our new profiles to traditional source profiles and various scaling approaches used previously to estimate IVOC emissions. These comparisons reveal large errors in these different approaches, ranging from failure to account for IVOC emissions (traditional source profiles) to assuming source-invariant scaling ratios (most IVOC scaling approaches).


2017 ◽  
Vol 607-608 ◽  
pp. 253-261 ◽  
Author(s):  
Wang Hong-li ◽  
Jing Sheng-ao ◽  
Lou Sheng-rong ◽  
Hu Qing-yao ◽  
Li Li ◽  
...  

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.


2014 ◽  
Vol 14 (3) ◽  
pp. 818-828 ◽  
Author(s):  
Hongli Wang ◽  
Shengrong Lou ◽  
Cheng Huang ◽  
Liping Qiao ◽  
Xibin Tang ◽  
...  

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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