Variations in physicochemical properties of airborne particles during a heavy haze-to-dust episode in Beijing
- 1. Institute of Surface-Earth System Science, School of Earth System Science, Tianjin University, Tianjin 300072 (China)
- 2. State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871 (China)
- 3. Key Laboratory of Resource Exploration Research of Hebei Province, Hebei University of Engineering, Handan 056038 (China)
Description
Highlights: • A typical transition from haze to dust was observed in Beijing. • Airborne particles were analyzed by single particle analysis combined with online aerosol mass spectrometry. • The dust plume brought mineral particles and freshly emitted particles and swept away secondary particles. • Photooxidation contributed secondary formation in dust episode while aqueous reaction dominated in haze episode. • The dust plume and local polluted air mixed slightly in the transition period. The variations in physicochemical properties of airborne particles collected during a typical transition from haze to dust were investigated using single particle analysis with transmission and scanning electron microscopes combined with online measurement of chemical compositions of airborne particles in Beijing in February 2013. The transition was divided into three phases based on the weather condition. During haze pollution (Phase 1), gaseous and particle pollutants enhanced gradually. Results from single particle analysis showed that more coatings and more anthropogenic elements (e.g., S) appeared on the surface of fine and coarse particles, which was probably caused by efficient aqueous-phase reactions under high humidity (70%) condition. Phase 2 was dust intrusion episode. PM10 reached over 1000 μg m−3. Larger fractions of mineral particles and bare-like soot particles were observed in fine particles, while the fraction of secondary particles with coatings decreased. The proportion of black carbon in submicron particles also increased. Photochemical oxidation in gas phase likely dominated in secondary formation under high O3 concentration. After the dust episode (Phase 3), secondary formation enhanced obviously. Soot aged quickly and had a larger mode of 0.45 μm than the other phases. The size modes of airborne fine particles during Phases 1 and 3 were 0.35 μm, which were a bit larger than that during Phase 2 (0.24 μm). These results indicate that dust plumes accompanied with strong wind brought mineral particles in both fine and coarse modes and freshly emitted particles with smaller sizes, and swept away pre-presence air pollutants. This study could provide detailed information on the physicochemical properties of airborne particles during typical severe pollution processes in a short time. Such short-term change should be taken into account in order to more accurately assess the environmental, climatic and health-related effects of airborne particles.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2020.143081Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2020.143081;
- PII
- S0048969720366110;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 762
- Journal Page Range
- vp.
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54061026
- Subject category
- S54: ENVIRONMENTAL SCIENCES; S46: INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY;
- Descriptors DEI
- AEROSOLS; AIR POLLUTION; CHEMICAL COMPOSITION; COARSE PARTICLES; COATINGS; ECOLOGICAL CONCENTRATION; EMISSION; FINE PARTICLES; HUMIDITY; MASS SPECTROMETERS; MASS SPECTROSCOPY; OXIDATION; PHOTOCHEMISTRY; POLLUTANTS; SCANNING ELECTRON MICROSCOPY; SOOT; SURFACES; WEATHER
- Descriptors DEC
- CHEMICAL REACTIONS; CHEMISTRY; COLLOIDS; COMBUSTION PRODUCTS; DISPERSIONS; ELECTRON MICROSCOPY; MEASURING INSTRUMENTS; MICROSCOPY; MOISTURE; PARTICLES; PARTICULATES; POLLUTION; SOLS; SPECTROMETERS; SPECTROSCOPY
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier B.V. All rights reserved.