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Lab-Scale Model to Evaluate Odor and Gas Concentrations Emitted by Deep Bedded Pack Manure
Published on: July 19, 2018
Impact of volatile organic compounds in large municipal solid waste landfills on regional environment
Liyuan Zhang1, Guanyu Nian2, Jiahao Zhong2
1School of Water and Environment, Chang'an University, Xi'an, China; Key Laboratory of Subsurface Hydrology and Ecological Effect in Arid Region of the Ministry of Education, Chang'an University, Xi'an, China; Key Laboratory of Eco-hydrology and Water Security in Arid and Semi-arid Regions of Ministry of Water Resources, Chang'an University, Xi'an, China.
Abstract:
Landfill disposal is a major approach of disposing municipal solid waste (MSW) in China. In order to explore the impact of volatile organic compounds (VOCs) generated by landfill on the air quality of regional environment, Jiangcungou landfill in Xi'an and its surrounding area were taken as a research object to analyze the spatial distribution and seasonal variation patterns of non-methane hydrocarbon (NMHC) and VOCs components through seasonal sampling of regional NMHC concentration and VOCs concentration (116 species). CALPUFF model was adopted to analyze the regional dispersion characteristics of NMHC on landfill. In addition, propylene equivalent concentration (PEC) and maximum incremental reactivity (MIR) methods were used to estimate O3 formation potential of the landfill, while fraction aerosol coefficient (FAC) and SOA potential (SOAP) methods were used to estimate SOA formation potential of the landfill. It was indicated that, the component with the highest concentration of VOCs on the working surface and the surrounding area of landfill was p + m-xylene (41.0 μg/m3) and halohydrocarbon (111.2 μg/m3-156.3 μg/m3), respectively. The component with the greatest impact on the surrounding air was acetone, which accounts for 75 %-87 % of the corresponding substance concentration on the landfill. In summer, the surrounding area was affected most by NMHC from landfill, whose emissions contributed 9.5 mg/m3 to the surrounding area. The component making the largest contribution to O3 formation was p + m-xylene (8 %-24 %), while ethylbenzene was the component making the largest contribution to SOA formation (20 %-24 %).
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