Multivariate analysis of carcinogenic equivalence (CEQ) to characterize carcinogenic VOC emissions in a typical petrochemical industrial park in Taiwan.

Large industrial emissions of volatile organic compounds (VOCs) from the petrochemical industry are a critical concern due to their potential carcinogenicity. VOC emissions vary in composition depending on the source and occur in mixtures containing compounds with varying degrees of toxicity. We proposed the use of carcinogenic equivalence (CEQ) and multivariate analysis to identify the major contributors to the carcinogenicity of VOC emissions. This method weights the carcinogenicity of each VOC by using a ratio of its cancer slope factor to that of benzene, providing a carcinogenic equivalence factor (CEF) for each VOC. We strategically selected a petrochemical industrial park in southern Taiwan that embodies the industry's comprehensive nature and serves as a representative example. The CEQs of different emission sources in three years were analyzed and assessed using principal component analysis (PCA) to characterize the major contributing sectors, vendors, sources, and species for the carcinogenicity of VOC emissions. Results showed that while the study site exhibited a 20.7 % (259.8 t) decrease in total VOC emissions in three years, the total CEQ emission only decreased by 4.5 % (15.9 t), highlighting a potential shift in the emitted VOC composition towards more carcinogenic compounds. By calculating CEQ followed by PCA, the important carcinogenic VOC emission sources and key compounds were identified. More importantly, the study compared three approaches: CEQ followed by PCA, PCA followed by CEQ, and PCA only. While the latter two methods prioritized sources based on emission quantities, potentially overlooking less abundant but highly carcinogenic compounds, the CEQ-first approach effectively identified vendors and sources with the most concerning cancer risks. This distinction underscores the importance of selecting the appropriate analysis method based on the desired focus. Our study highlighted how prioritizing CEQ within the analysis framework empowered the development of precise control measures that address the most carcinogenic VOC sources.

Modelling chloroform in indoor swimming pool air and water: the influences of internal air circulation and occupants.

The release of chloroform from water to air in an indoor swimming pool (ISP) exhibits complex physicochemical interactions among many variables, including environmental conditions, occupant activities, and geometry of the ISP. By combining the relevant variables, a structured mathematical model, the double-layer air compartment (DLAC) model, was developed to predict the level of chloroform in ISP air. A physical parameter, the indoor airflow recycle ratio (R), was incorporated into the DLAC model due to internal airflow circulation resulting in the ISP structural configuration. The theoretical R-value for a specific indoor airflow rate (vy) can be found by fitting the predicted residence time distribution (RTD) to the simulated RTD from computational fluid dynamics (CFD), showing a positive linear relationship with vy. The mechanical energies induced by occupant activities were converted into a lumped overall mass-transfer coefficient to account for the enhanced mass transfer of chloroform from the water into the air and mixing in ISP air. The DLAC model predicted that chloroform air concentrations were statistically less accurate without considering the influence of R compared with the online open-path Fourier transform infrared measurements. A novel index, the magnitude of emission (MOE) from swimmers, was linked to the level of chloroform in ISP water. The capability of the DLAC model associated with the MOE concept may facilitate upgrading the hygiene management of ISPs, including the ability to administer necessary chlorine additives in pool water and monitor the chloroform in ISP air.

Simulating the spatiotemporal distribution of BTEX with an hourly grid-scale model.

Modeling approaches have been utilized to simulate ambient pollutant concentrations, but very limited efforts have been made to estimate volatile organic compounds in the atmosphere. For this reason, an hourly grid-scale simulation model was developed to determine ambient air concentrations of benzene, toluene, ethylbenzene, and xylene (BTEX). BTEX data were collected over a one-year time frame from the database of the Taiwan Environmental Protection Administration's photochemical assessment monitoring stations. Multivariate linear regression models were used along with correlation analysis to simulate hourly grid-scale BTEX concentrations, using criteria pollutants and selected meteorological variables as predictors. The simulation model was validated in the southern Taiwan area via a portable micro gas chromatography system (n = 121) with significant correlation (r = 0.566**, ** indicated p < 0.01). Moreover, the grid-scale model was applied to areas covering about 72% of the population in Taiwan. A geographic information system (GIS) was used to visualize the spatial distribution of BTEX concentrations from the modeling results. This new grid-scale modeling strategy, which incorporated the GIS output of the simulated data, provides a useful alternative tool for personal exposure analysis and health risk assessment of ambient air BTEX.

Cadmium adsorption on goethite-coated sand in the presence of humic acid.

Heat was employed to coat crystalline goethite onto a quartz sand surface so that the adsorbent properties of the coating could be utilized. The adsorption characteristics of cadmium and humic acid onto goethite-coated sand were examined. Results show that the goethite-coated sand surface had a higher specific surface area and more mesopores than the uncoated sand. The adsorption of both cadmium and humic acid was highly pH-dependent: cadmium adsorption increased with pH, but humic acid adsorption decreased as pH increased. The presence of humic acid resulted in increasing cadmium adsorption in a specific pH range. The order of reacting humic acid with cadmium was found to have a noticeable effect on the final adsorption capacity. The adsorption capacity of cadmium for humic acid that is adsorbed onto goethite-coated sand before reacting with a cadmium system, exceeds that of humic acid that is mixed with cadmium ions before goethite-coated sand is added.

Vertical ozone distributions observed using tethered ozonesondes in a coastal industrial city, Kaohsiung, in southern Taiwan.

This work presents the vertical distributions of ozone and meteorological parameters observed with tethered ozonesondes and meteorological radiosondes in the lower atmosphere during an ozone episode on March 25-27, 2003, in Kaohsiung City in southern Taiwan. Kaohsiung is a coastal industrial city with inland mountain ranges to the east. Extremely complicated ozone structures were identified that spanned day and night during the experimental period. During afternoons, the lower atmosphere was divided into two stratified air layers with substantially different ozone concentrations. On the episode day (March 26), average ozone concentration in the near-ground layer was 85 ppb and the aloft layer was 140 ppb. A very high ozone peak of 199 ppb measured aloft likely resulted from an elevated large point source. Several no-ozone air layers, distributed throughout 400-750 m, were observed to transport on shore during the night. As well, elevated ozone layers peaking at 60-90 ppb and 90-160 ppb were detected below and above the no-ozone air layers, respectively. These complicated ozone structures were likely formed through titration of plumes from large point sources and the circulations of sea breezes or combined sea-breeze/mountain flows in the study area.