RESUMO
This study evaluated the performance of TiO2-ZnO/biochar as activator of persulfate (PS) for degradation of furfural. After the successful synthesis of the catalyst, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) methods were used to investigate the properties of TiO2-ZnO/biochar. The findings of this research suggests that under optimal conditions (pH = 3, catalyst dosage = 1 g/L, persulfate concentration = 1.2 mM, and furfural concentration = 10 mg/L), the PS/Catalysts/UV system can remove 96 % of furfural within 15 min. Under ideal conditions, the experimental results fit well with the first-order kinetic model (R2 > 0.95), and the rate constant (Kobs) was derived as 0.195 min-1. The quenching experiments provided further insights that confirmed the participation of SO4°- and OH° radicals in the degradation process. Nevertheless, the evidence strongly supports the idea that SO4°- plays a more prominent and dominant role as the primary radical species responsible for furfural degradation. Based on the obtained results, it can be concluded that the PS/Catalysts/UV system has an appropriate ability to remove furfural from aqueous solutions, which suggests promising perspectives for its practical application in pollutant treatment scenarios.
RESUMO
This study investigates the concentrations of PM10-bound PAHs and their seasonal variations in three cities of Ahvaz, Abadan, and Asaluyeh in Iran. The mean concentrations of PM10 in two warm and cold seasons in Ahvaz were higher and in Abadan and Assaluyeh were lower than the national standard of Iran and the guidelines of the World Health Organization. The Σ16 PAHs concentration in ambient air PM10 during the cold season in Ahvaz, Abadan and Asaluyeh was 244.6, 633, and 909 ng m- 3, respectively, and during the warm season in Ahvaz, Abadan, and Asaluyeh was 242.1, 1570 and 251 ng m- 3, respectively. The high molecular weight PAHs were the most predominant components. The most abundant PAHs species were Pyr, Chr, B [ghi] P, and Flt. The results showed that the total PAHs concentration in the cold and warm seasons was dependent on industrial activities, particularly the neighboring petrochemical units of the city, vehicular exhausts, traffic and use of oil, gas, and coal in energy production. The total cancer risk values as a result of exposure to PAHs in ambient air PM10 in all three cities for children and adults and in both cold and warm seasons were between 1 × 10- 6 and 1 × 10- 4, and this indicates a potential carcinogenic risk. Therefore, considering the various sources of air pollutants and its role on people's health, decision makers should adopt appropriate policies on air quality to reduce the ambient air PAHs and to mitigate human exposure.