State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090, PR China.
Bioresour Technol. 2013 Jan;128:827-30. doi: 10.1016/j.biortech.2012.10.086. Epub 2012 Oct 29.
This study aimed to prove the promotion effects of ultrasonic on malachite green (MG) decolorization in the ultrasonic-assisted ozone oxidation process (UAOOP), and propose the possible pathway of MG degradation. The decolorization of MG followed an apparent pseudo first-order kinetic law (initial MG concentration 100-1000 mg/L). When ultrasonic (US) was applied with ozone simultaneously, the apparent pseudo-first-order rate constant (K(app)) increased, and the time MG decolorized to the half of initial concentration (T(1/2)) shortened 185 s (1000 mg/L). Moreover, the stoichiometric ratio (Z(app)) between O(3) and MG was enhanced by US to 2.0 mol, saving 11% oxidant addition, comparing to individual ozone process. These results indicated that the application of US can reduce reaction time and dose of ozone addition. The possible pathway of MG degradation included three major approaches. And the result suggested that the reaction between MG and hydroxyl radical was substitution reaction rather than adduct reaction.
本研究旨在证明超声在超声辅助臭氧氧化过程(UAOOP)中对孔雀石绿(MG)脱色的促进作用,并提出 MG 降解的可能途径。MG 的脱色符合明显的准一级动力学规律(初始 MG 浓度 100-1000mg/L)。当同时施加超声(US)和臭氧时,表观准一级速率常数(K(app))增加,MG 褪色至初始浓度一半的时间(T(1/2))缩短了 185s(1000mg/L)。此外,US 将 O(3)和 MG 的化学计量比(Z(app))提高到 2.0mol,与单独的臭氧过程相比,节省了 11%的氧化剂添加量。这些结果表明,US 的应用可以减少反应时间和臭氧添加量。MG 降解的可能途径包括三种主要方法。结果表明,MG 与羟基自由基之间的反应是取代反应而不是加合反应。