In this study, the ambient concentrations of volatile organic compounds (VOCs) were intensively measured from January 2012 to December 2016 using an evacuated canister and were analyzed using a gas chromatography/mass spectrophotometer (GC/MS) based on the US EPA TO-15 in the community and industrial areas of the largest petroleum refinery and petrochemical industrial complex in Map Ta Phut Thailand. The ternary diagram was used to identify the source of VOCs. Reactivity of VOCs on their ozone formation potential (OFP) were quantified by the maximum incremental reactivity coefficient method (MIR) and propylene-equivalent concentration methods. Results from the study revealed that aromatic hydrocarbon was the dominant group of VOCs greatly contributing to the total concentration of measured VOCs. Among the measured VOCs species, toluene had the highest concentration and contributed as the major precursor to ozone formation. The ternary analysis of benzene:toluene:ethybenzene ratios indicated that VOCs mainly originated from mobile sources and industrial processes. Within the industrial area, measured VOC concentration was dominated by halogenated hydrocarbons, and alkene was the highest contributor to ozone formation. The propylene-equivalent concentration method was also used to evaluate the reactivity of VOCs and their role in ozone formation, and secondly to support findings from the MIR method.

Automotive manufacturing is one of the potential sources of air pollution particularly involving volatile organic compounds (VOCs). This study intensively evaluated VOC emissions and their dispersion from the industry. The measured VOCs were speciated for further evaluation of their odor threats according to the characteristics of each compound. Mathematical emission and air dispersion models were applied to assist in elaborating the source–receptor relationship allowing the determining of existing business-as-usual conditions with proposed mitigation measures to manage the pollution of the factory studied in this paper. Seven VOC species potentially caused odor problems to the surrounding community, including 1-butanol, ethyl benzene, toluene, m,p xylene, o xylene, methyl ethyl ketone, and methyl isobutyl ketone. The results from the AERMOD dispersion model revealed that the smell from these chemicals could reach up to about 800 m from the source. Analysis of mitigation measures indicated that two interesting scenarios should be considered according to their effectiveness. The concentrations of VOCs can decrease by up to 4.7, 14.0 and 24.9% from increasing the physical stack height by +1, +3 and +5 m from its existing height, respectively. Modification of the aeration tank of the wastewater treatment unit to a closed system also helped to reduce about 27.8% of emissions resulting in about a 27.6% decreased ambient air concentration. This study provided useful information on the characteristics of VOCs emitted by the automobile manufacturing industry. It also demonstrated the relevant procedures and highlights the necessity to comprehensively analyze the source–receptor relationship to evaluate the most appropriate measures in managing industrial air pollution.

Secondary organic aerosol (SOA), a key constituent of fine particulate matter, can be formed through the oxidation of volatile organic compounds (VOCs). However, information on its relevant emission sources remains limited in many cities, especially concerning different types of land use. In this study, VOC concentration in Bangkok Metropolitan Region (BMR), Thailand, was continuously collected for 24 h by 6-L evacuated canister and analyzed by gas chromatography/mass spectrophotometry following USEPA TO15, and the formation of SOA was evaluated through the comprehensive direct measurements and speciation of ambient VOCs. Finally, source contribution of VOCs to SOA formation was characterized using the Positive Matrix Factorization (PMF) model. The results revealed the abundant group of VOCs species in the overall BMR was oxygenated VOCs, accounting for 49.97-57.37%. The SOA formation potential (SOAP) ranged from 1,134.33 to 3,143.74 μg m −3 . The VOC species contributing to the highest SOAP was toluene. Results from the PMF model revealed the dominant emission source of VOCs that greatly contributed to SOA was vehicle exhaust emission. Industrial combustion was the main source of VOC emission contributing to SOA in industrial areas. Sources of fuel evaporation, biomass burning, and cooking were also found in the study areas but in small quantities. The results of this study elucidated that different emission sources of VOCs contribute to SOA with respect to different types of land use. Findings of this study highlight the necessity to identify the contribution of potential emission sources of SOA precursors to effectively manage urban air pollution.

Buoyancy and momentum fluxes are important parameters to determine the plume rise which is related to the ability to dilute air pollutants emitted from combustion stack sources. The change of temperature due to waste heat recovery directly affects these fluxes. This study analyzed buoyancy and momentum fluxes and evaluated the ground level concentration of PM-10 prior and after implementation of waste heat recovery in the area surrounding one of the largest cement production plants in Thailand. The results showed that the ambient temperature was the significant parameter affecting buoyancy and momentum fluxes. The buoyancy flux was found to be the dominant force to the rise of plume for both scenarios. There were no differences in the predicted PM-10 ground level concentrations at receptors around the cement plant for the model simulation under two scenarios. Therefore, it was concluded that decreasing of stack gas exit temperature does not affect the dispersion of air pollutants in the cement industry.

The emission inventory, emission factor, and spatial concentration distribution of volatile organic compounds (VOCs) from a petrochemical industry (aromatics plant) were intensively evaluated in this study to elucidate the potential sources of BTX emission and their contribution to ambient concentrations. Five emission groups were quantified through direct measurement and emission models. These data were then used as input for the AERMOD dispersion model for the source apportionment analysis. The source to ambient contribution analysis revealed that a wastewater treatment facility and organic liquid storage tank were major contributors accounting for about 20.6–88.4% and 10.3–75.4% to BTX environmental concentrations, respectively. The highest annual ambient concentrations of benzene (B), toluene (T), and xylenes (X) were predicted as 9.0, 2.8, and 57.9 µg/m3 at the fence line of the plant boundary, respectively. These findings assist policymakers in prioritizing the appropriate control measures to the right source by considering not just the amount released but also their contribution to ambient concentrations. This study suggested that the wastewater treatment unit should be changed to the closed system which will benefit reduction in its emission (45.05%) as well as effectively minimizing ambient VOC concentration by 49.96% compared to its normal operation.