Gültekin I, Ince N H
Institute of Environmental Sciences, Bogazici University, 34342 Bebek, Istanbul, Turkey.
Ultrason Sonochem. 2006 Apr;13(3):208-14. doi: 10.1016/j.ultsonch.2005.03.002. Epub 2005 Jun 1.
Lab-scale degradation of azo dyes with ultrasound (300 kHz), ozone and both was investigated using an aryl-azo-naphthol dye-C.I. Acid Orange 8. It was found that in all schemes color decay was faster than UV absorbance, and the rates followed pseudo-first-order kinetics except for the decay of UV-254 band by ozone. Sonication alone was sufficient for decolorization, but not for UV absorption abatement or mineralization. Ozonation was more effective than ultrasound in bleaching, but not as much for the mineralization of the dye. Combined operation of ultrasound and ozone improved the rate of bleaching and UV absorption decay and remarkably enhanced the mineralization of the dye. This was attributed to increased mass transfer of ozone in solution and its decomposition in the gas phase to yield hydroxyl radicals and other oxidative species. The effect of alpha-methyl substituent at the aryl carbon of the dye was found to decelerate the rate of degradation as a result of weakened intramolecular hydrogen bonding.
使用一种芳基偶氮萘酚染料——C.I.酸性橙8,研究了实验室规模下超声(300 kHz)、臭氧以及二者联合对偶氮染料的降解情况。结果发现,在所有方案中,颜色衰减都比紫外吸光度快,除了臭氧对UV - 254波段的衰减外,降解速率均遵循准一级动力学。单独超声处理足以实现脱色,但不足以降低紫外吸收或实现矿化。臭氧化在漂白方面比超声更有效,但在染料矿化方面效果不如超声。超声和臭氧联合操作提高了漂白速率和紫外吸收衰减速率,并显著增强了染料的矿化程度。这归因于溶液中臭氧传质的增加及其在气相中的分解,从而产生羟基自由基和其他氧化物种。研究发现,由于分子内氢键减弱,染料芳基碳上的α - 甲基取代基会降低降解速率。