Significant concentration changes of chemical components of PM1 in the Yangtze River Delta area of China and the implications for the formation mechanism of heavy haze–fog pollution
Creators
- 1. Key Laboratory of Atmospheric Chemistry, Chinese Academy of Meteorological Sciences, Beijing 100081 (China)
- 2. State Key Laboratory of Cryospheric Sciences, Cold and Arid Region Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000 (China)
- 3. Lin'an Regional Air Background Station, Lin'an 311307 (China)
- 4. School of Atmospheric Sciences, Nanjing University, Nanjing 210093 (China)
- 5. College of Earth Science, University of Chinese Academy of Sciences, Beijing 100049 (China)
Description
Since the winter season of 2013, a number of persistent haze–fog events have occurred in central-eastern China. Continuous measurements of the chemical and physical properties of PM1 at a regional background station in the Yangtze River Delta area of China from 16 Nov. to 18 Dec., 2013 revealed several haze–fog events, among which a heavy haze–fog event occurred between 6 Dec. and 8 Dec. The mean concentration of PM1 was 212 μg m−3 in the heavy haze–fog period, which was about 10 times higher than on clean days and featured a peak mass concentration that reached 298 μg m−3. Organics were the largest contributor to the dramatic rise of PM1 on heavy haze–fog days (average mass concentration of 86 μg m−3), followed by nitrate (58 μg m−3), sulfate (35 μg m−3), ammonium (29 μg m−3), and chloride (4.0 μg m−3). Nitrate exhibited the largest increase (~ 20 factors), associated with a significant increase in NOx. This was mainly attributable to increased coal combustion emissions, relative to motor vehicle emissions, and was caused by short-distance pollutant transport within surrounding areas. Low-volatility oxidized organic aerosols (OA) (LV-OOA) and biomass-burning OA (BBOA) also increased sharply on heavy haze–fog days, exhibiting an enhanced oxidation capacity of the atmosphere and increased emissions from biomass burning. The strengthening of the oxidation capacity during the heavy pollution episode, along with lower solar radiation, was probably due to increased biomass burning, which were important precursors of O3. The prevailing meteorological conditions, including low wind and high relative humidity, and short distance transported gaseous and particulate matter surrounding of the sampling site, coincided with the increased pollutant concentrations mainly from biomass-burning mentioned above to cause the persistent haze–fog event in the YRD area. - Highlights: • Formation mechanism of a heavy haze-fog event that occurred in the YRD region of china was discussed. • Nitrate exhibited the largest increase on the heavy haze-fog days. • Increased biomass burning and atmospheric oxidizing capacity were the major reasons for the significant increase of OA. • Short-distance transport, low wind speed and high RH were highly responsible for the formation of the pollution event.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2015.06.104Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2015.06.104;
- PII
- S0048-9697(15)30301-6;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 538
- Journal Page Range
- p. 7-15
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48010933
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- AEROSOLS; BIOMASS; CHEMICAL COMPOSITION; CHINA; CHLORIDES; COAL; COMBUSTION; CONCENTRATION RATIO; ECOLOGICAL CONCENTRATION; EXHAUST GASES; FOG; NITRATES; NITROGEN OXIDES; OZONE; PARTICULATES; POLLUTANTS; POLLUTION; RIVER DELTAS; SULFATES; YANGTZE RIVER
- Descriptors DEC
- ASIA; CARBONACEOUS MATERIALS; CHALCOGENIDES; CHEMICAL REACTIONS; CHLORINE COMPOUNDS; COASTAL REGIONS; COLLOIDS; DIMENSIONLESS NUMBERS; DISPERSIONS; ENERGY SOURCES; FLUIDS; FOSSIL FUELS; FUELS; GASEOUS WASTES; GASES; HALIDES; HALOGEN COMPOUNDS; MATERIALS; NITROGEN COMPOUNDS; OXIDATION; OXIDES; OXYGEN COMPOUNDS; PARTICLES; RENEWABLE ENERGY SOURCES; RIVERS; SOLS; SULFUR COMPOUNDS; SURFACE WATERS; THERMOCHEMICAL PROCESSES; WASTES
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.