Shipping-related air pollution at Busan Port: The unceasing threat of black carbon

被引:0
|
作者
Loh, Andrew [1 ]
Kim, Donghwi [1 ]
An, Joon Geon [1 ]
Hyun, Sangmin [2 ]
Yim, Un Hyuk [1 ,3 ]
机构
[1] Korea Inst Ocean Sci & Technol, Oil & POPs Res Grp, Geoje 53201, South Korea
[2] Korea Inst Ocean Sci & Technol, Marine Environm Res Ctr, Busan 49111, South Korea
[3] Korea Univ Sci & Technol, Dept Ocean Sci, Daejeon 34113, South Korea
关键词
Busan Port; Sub-micron aerosols; Black carbon; Emission sources; Seasonal variation; RESOLVED CHEMICAL-CHARACTERIZATION; AEROSOL CHEMISTRY; ORGANIC AEROSOLS; LIGHT-ABSORPTION; LONG-RANGE; MASS; CITY; PARTICLES; SECONDARY; SUMMERTIME;
D O I
10.1016/j.jhazmat.2025.137434
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Busan Port ranks among the top ten most air-polluted ports globally, yet the chemical characteristics of its air pollution, specifically the compositions and sources of aerosols, including black carbon (BC) have not been thoroughly studied. To assess the emission characteristics, four comprehensive air monitoring campaigns were conducted seasonally from fall 2020 to summer 2021. While mass concentrations of aerosol chemical species analyzed using the high-resolution time-of-flight aerosol mass spectrometer showed significant seasonal variations (3.6-11.4 mu g center dot m- 3), BC exhibited persistent concentrations throughout all seasons (1.9-2.2 mu g center dot m- 3). On average, BC constituted a staggering 26.5 % of the total non-refractory sub-micron aerosol mass concentrations. A positive matrix factorization model used to identify organic aerosol (OA) sources revealed six sources: two hydrocarbon-like OA, three oxygenated OA, and one biomass burning OA. Most of these sources were associated with shipping-related emissions at Busan Port. Spatial analysis of the elemental carbon revealed higher concentrations in port areas (1.2-1.5 mu g center dot m-3) and surrounding areas (0.6-1.0 mu g center dot m-3), compared to other urban cities (0.5-0.6 mu g center dot m- 3). This observation suggests that carbonaceous particles, along with persistent shippingrelated OA emissions, are likely to disperse and impact air quality in adjacent urban areas, potentially posing health hazards.
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