An original ultrasound (US) directly intensified photocatalytic reactor was designed to degrade azo dye pollutant methyl orange (MeO) using Degussa TiO(2) as the photocatalyst. The sonolytic, photocatalytic and sonophotocatalytic degradation of MeO in the new reactor and the synergistic effect between sonolysis and photocatalysis were investigated. Effects of operation parameters i.e., US power, TiO(2) dosage, liquid circulation velocity and air flow rate on degradation efficiency were investigated and optimized. The results showed that all parameters have optimal values for the sonophotocatalytic degradation of MeO, and the optimum conditions for the new process are US power 600 W, TiO(2) dosage 3g/L, liquid circulation velocity 4.05×10(-2) m/s and air flow rate 0.2 L/min. Under the optimum conditions, 91.52% MeO had been degraded within 1h, and the combination of sonolysis and TiO(2) photocatalysis exhibited an obvious synergetic effect.
The potential of TiO2-based photocatalysts in mitigating the effects of environmental pollutants is evident in the scientific literature but the large-scale implementation of photocatalytic concretes still appears limited, despite the current global concerns over urban NOx pollution. Improvements in cost-effectiveness are required to enhance the case for a photocatalyst-modified infrastructure and this must address catalyst efficiency, catalyst loading and performance durability. This paper compares photocatalytic efficiencies of TiO2 supported on mortar surfaces with the more conventional TiO2 dispersed in mortar. The influences of environmental conditions, such as NO concentration and flow rate, UVA light intensity and relative humidity, on photocatalytic performance are also investigated using photonic efficiency as an indicator. The supported TiO2 shows greater degradation of NOx (De-NOx), at about 9 times higher than TiO2 powder dispersed in the mortar, ca. 150 times higher utilization efficiency, than that of TiO2 in traditional photocatalytic mortar (with 5% loading).
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