Min-Suk Bae’s research while affiliated with Mokpo National University and other places

Volatile organic compounds (VOCs) play a critical role in atmospheric chemistry, contributing to the formation of ozone, secondary PM2.5 production, and global warming. This study investigates the spatial distribution and long-range transport dynamics of VOCs over South Korea, using airborne observations conducted during the 2024 Asian Air Quality campaign. VOC concentrations were measured in urban, industrial, and long-range transport scenarios using proton transfer reaction-time-of-flight mass spectrometry (MS) and gas chromatography–MS with canister sampling. The results demonstrate that benzene shows significant vertical and spatial dispersion during long-range transport due to its intermediate atmospheric lifetime, which allows it to persist and impact downwind air quality. Additionally, Chlorinated VOCs, such as 1,2-dichloroethane and 1,2,4-trichlorobenzene, display transport behaviors. Their relatively consistent concentrations during long-range transport emphasize the influence of industrial activities, including coal combustion and petrochemical processes, as major sources. Elevated levels of chlorinated VOCs were primarily associated with emissions from industrial regions in Chungnam, while aromatic VOCs were predominantly linked to urban traffic emissions. These findings underscore the need for international cooperation to combat transboundary pollution and highlight the importance of comprehensive air quality management strategies that address both urban and industrial emission sources. This study provides essential insights into the atmospheric behavior of VOCs and emphasizes the need for targeted policies to effectively regulate air pollution.

PM2.5 samples were collected in Suncheon during the summer (June 2–11, 2023) and winter (January 15–21, 2024). The chemical composition analysis included carbonaceous components (OC, EC), secondary ionic components (NH4⁺, NO3⁻, SO4²⁻), dithiothreitol - oxidative potential (QDTT-OP), and volatile organic compounds. Results showed higher summer PM2.5 concentrations due to photochemical reactions and higher winter concentrations from heating and stable atmospheric conditions. The OC/EC ratio indicated greater secondary organic aerosol formation in summer. Oxidative potential (QDTT-OPv) was higher in summer (0.12 µM/m³) than winter (0.09 µM/m³), correlating strongly with OC in summer. Health risk assessment of BTEX revealed higher concentrations in winter, with benzene as the primary contributor to lifetime cancer risk (LTCR). The cumulative hazard quotient (HQ) was higher in winter, indicating increased non-carcinogenic risk. The study highlighted that oxidative potential is more influenced by chemical composition than physical characteristics, suggesting that regulating PM2.5 concentration alone may be insufficient. VOCs, as precursors of SOA, showed a positive correlation with QDTT-OPv, with benzene exhibiting the strongest correlation in winter. These findings emphasize the need for targeted management of specific PM2.5 components to mitigate health risks effectively. Graphical Abstract

This study evaluated the health risks and chemical composition of PM1.0 and PM2.5 in Incheon, South Korea, emphasizing the critical role of particle size in public health impacts. The average concentrations were 10.89 μg/m³ for PM2.5 and 8.11 μg/m³ for PM1.0. PM1.0 displayed higher proportions of carbonaceous components and water-soluble ions, predominantly formed through photochemical reactions and atmospheric chemistry processes. Health risk assessments, using the Benzo [a]pyrene toxic equivalency factor, mutagenic and carcinogenic potential, risk index, and oxidative potential (DTT-OP), indicated that PM1.0 poses significantly higher health risks per unit mass compared to PM2.5. Key components in PM1.0, such as levoglucosan and terephthalic acid (TPA), indicate significant contributions from combustion sources like biomass burning and plastic incineration, particularly at night. PM1.0 showed higher carcinogenic and mutagenic risks than PM2.5. The correlation between levoglucosan, PAHs, and TPA supports common combustion origins. Effective management of combustion-related emissions is crucial for reducing health risks associated with PM1.0. The overall average risk index for PM1.0 is 1.30 times higher than PM2.5, implying that, on average, PM1.0 poses a 30 % higher health risk across the measured indices compared to PM2.5. This study emphasizes the need for targeted management of combustion emissions, particularly those from plastic and fuel combustion, to mitigate the health risks posed by PM1.0. Effective control of the precursors contributing to PM1.0 formation is crucial for reducing the adverse health impacts of air pollution.

This study evaluates the composition and seasonal characteristics of fine particulate matter (PM2.5) during winter and summer through simultaneous measurements conducted at the Gwangju Institute of Science and Technology in South Korea and the Changping campus of Peking University in China. PM2.5 samples were concurrently collected at both sites, and chemical analyses were conducted to quantify various components, including carbonaceous materials, ionic species, and metals. Although the average PM2.5 concentrations were comparable between the two sites, there were distinct differences in the concentrations of major components. Organic indicator compounds were analyzed to discern the contributions of primary and secondary pollution sources. Changping displayed a mix of primary and secondary pollution, characterized by higher concentrations of primary organic carbon (POC) such as polycyclic aromatic hydrocarbons and hopanes, compared to Gwangju. In contrast, Gwangju demonstrated a higher prevalence of secondary organic carbon (SOC), particularly water-soluble organic carbon not related to biomass burning (WSOCnbb) and various polar organic compounds. The organic mass to organic carbon (OM/OC) ratios estimated using the mass balance method revealed significant differences, with Gwangju showing a higher ratio of 2.3 compared to 1.9 at Changping, indicating a greater influence of secondary pollutants at Gwangju. Additionally, both Changping and Gwangju exhibited higher OM/OC ratios in summer (Changping: 2.0, Gwangju: 2.5) compared to winter (Changping: 1.8, Gwangju: 2.2), indicating seasonal differences in organic mass contributions to PM2.5. These findings underscore the importance of accounting for spatial and seasonal variations in air pollution studies and suggest that updating commonly used OM/OC ratios could enhance the reliability of research outcomes.

This study explores the efficiency and applicability of a HONO collection system that incorporates an ultrasonic nozzle and spray chamber for the measurement of ambient air. The system demonstrates (1) a remarkable efficiency of 97.7% across two serial stages, (2) lower detection limits of 0.15 ppbv for HONO, and (3) an absence of interference from NO2 or OH radicals. Practical ambient monitoring with the HONO collection system revealed typical diurnal variations in HONO, O3, and HNO3 concentrations, aligning with photolysis dynamics. Notably, HONO concentrations peaked at 0.37 ppb during nighttime and decreased to 0.27 ppb by midday. O3 demonstrated an inverse relationship with HONO, especially during ozone depletion phases, with r2 values of 0.94, 0.81, and 0.52 across various intervals. The HONO/NOx ratio during periods of enhanced HONO suggested the presence of additional formation mechanisms beyond heterogeneous NOx reactions. Moreover, ozone levels often fell below 20 ppb, indicating a consistent inverse correlation with HONO, thereby reaffirming further mechanisms of HONO formation beyond heterogeneous NOx reactions. The real-time atmospheric chemical reactions involving HONO, monitored concurrently with O3 and NOx, were effectively validated by the HONO collection system employed in this investigation.