ABSTRACT
Comparative degradation of azo dyes by 520 kHz ultrasonic irradiation and its combinations with ozone and/or ultraviolet light (UV) was investigated using a probe dye C.I. Acid Orange 7. Operation parameters such as ultrasonic power density, ozone flow, UV intensity, and type and injection mode of the bubbling gas were optimized based on the rate of absorption decay in the visible and UV bands as estimated by regression analysis of absorption-time data. At equivalent initial dye concentrations and contact times, individual effects of UV irradiation, ultrasound and ozone were "no effect", "bleaching", and "bleaching/organic carbon degradation", respectively. UV irradiation, however, was found to induce a catalytic effect when applied in combination with either ultrasound or ozone schemes; and the overall degradation process was most rapid under simultaneous operation of the three in the presence of a continuous flow of a gas mixture made of argon and oxygen. The synergy observed in combined schemes was attributed to enhanced ozone diffusion by mechanical effects of ultrasound, and the photolysis of ultrasound-generated H(2)O(2) to produce hydroxyl radicals.
ABSTRACT
Degradability of four textile dyes was investigated in deionized water solutions during 520 kHz ultrasonic irradiation. It was found that for all dyes, the rate of color decay was first order in the visible absorption of the dye, and related to the type of functional groups that characterized the chromophore in the dye molecules. The destruction of aromatic/olefinic carbons in azo dyes was slower than that of color--to be attributed to the priority of hydroxyl radical attack on the N=N bonds, and to the formation of numerous oxidation intermediates of organic character during the course of dye degradation. Toxicity analysis of the dye solutions prior to sonolysis revealed that "reactive" dyes were non-toxic, but "basic" ones were toxic at the test concentrations employed in the study. Significant degrees of toxicity reduction were accomplished along with color and aromatic carbon degradation.
