Distribution and gas-particle partitioning of polycyclic aromatic hydrocarbons over the East China Sea and Yellow Sea in spring: Role of atmospheric transport transition
- 1. Institute of Eco-Chongming (IEC), Shanghai 200062 (China)
- 2. Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Institute of Atmospheric Sciences, Department of Environmental Science and Engineering, Fudan University, Shanghai 200433 (China)
- 3. College of Resources and Environment, Shanxi University of Finance and Economics, Taiyuan 030006 (China)
- 4. College of Marine Ecology and Environment, Shanghai Ocean University, Shanghai 201306 (China)
- 5. College of Marine Geosciences, Key Laboratory of Submarine Geosciences and Prospecting Technology, Ocean University of China, Qingdao 266100 (China)
Description
Highlights: • PAH pollution greatly varied over the YS and the ECS in mid-spring. • PAH distribution pattern was controlled by regional atmospheric transport transition. • Koa-based model well predicted HMW PAHs partitioning in land air masses. • Adsorption onto soot notably impacted the gas-particle partitioning of PAHs. To elucidate the variations in the East Asian monsoon system during seasonal changes and their impacts on continental outflow of polycyclic aromatic hydrocarbons (PAHs), sixteen integrated air samples were collected during a research cruise covering the Yellow Sea (YS) and East China Sea (ECS) in mid-spring of 2017. The concentrations of total suspended particle (TSP), aerosol-phase PAH fractions, ratios of organic to elemental carbon (OC/EC) and gas-particle partitioning of atmospheric PAHs exhibited clear regional differences associated with variations in the monsoon regime. The total concentrations of 16 USEPA priority PAHs (Σ16PAHs) varied from 3.11 to 13.4 ng/m3 throughout the cruise, with medium-to-high molecular weight (MW) PAHs more enriched over the YS and north ECS than the south ECS. Together with the relatively low gaseous PAH fraction over the YS and north ECS (78 ± 4%) relative to the south ECS (95 ± 13%), this result indicates the pattern of regional atmospheric transport. The ratio of organic to elemental carbon varied significantly between the south ECS (lower than 4) and the YS and north ECS (greater than 4), indicating contributions from vehicle emissions and coal combustion or biomass burning, respectively, following different atmospheric input pathways of carbonaceous aerosols, as supported by backward trajectory analysis. Considering the gas-particle partitioning of PAHs, soot adsorption was the main partitioning mechanism in the study region; while high-MW PAHs in the YS and north ECS were influenced by both absorption and adsorption. The Koa absorption model provided better predictions for high-MW PAHs when continental air masses prevailed, despite underestimating the partition coefficients (kp) of low-MW PAHs. Meanwhile, predicted kp for medium MW PAHs was better estimated over the YS and ECS when Ksa was included.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2020.143071Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2020.143071;
- PII
- S0048969720366018;
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
- 54061072
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ABSORPTION; ADSORPTION; AEROSOLS; BIOMASS; CARBON; CHINA SEA; COAL; ECOLOGICAL CONCENTRATION; EMISSION; LINEAR ABSORPTION MODELS; MOLECULAR WEIGHT; MONSOONS; POLLUTION; POLYCYCLIC AROMATIC HYDROCARBONS; TOTAL SUSPENDED PARTICULATES
- Descriptors DEC
- AROMATICS; CARBONACEOUS MATERIALS; COLLOIDS; DISPERSIONS; ELEMENTS; ENERGY SOURCES; FOSSIL FUELS; FUELS; HYDROCARBONS; MATERIALS; MATHEMATICAL MODELS; NONMETALS; ORGANIC COMPOUNDS; PACIFIC OCEAN; PARTICLE MODELS; PARTICLES; PARTICULATES; RENEWABLE ENERGY SOURCES; SEAS; SOLS; SORPTION; STORMS; SURFACE WATERS
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier B.V. All rights reserved.