Aquino José M, Miwa Douglas W, Rodrigo Manuel A, Motheo Artur J
São Carlos Institute of Chemistry, University of São Paulo, P.O. Box 780, CEP 13560-970, São Carlos, SP, Brazil.
Department of Chemical Engineering, Faculty of Chemical Sciences & Technologies, Universidad de Castilla - La Mancha, Campus Universitario s/n, 13071, Ciudad Real, Spain.
Chemosphere. 2017 Apr;172:185-192. doi: 10.1016/j.chemosphere.2016.12.154. Epub 2017 Jan 2.
The photo-assisted electrochemical degradation of a real effluent of the atrazine manufacturing process containing atrazine, simazine, hydroxy-triazine and propazine was carried out galvanostatically using a pilot-scale tubular flow reactor prototype containing DSA and Ti as cathode. The effluent was mainly characterized by a high amount of NaCl, required in the synthesis route used, and it was used as taken in the factory. The variables for process optimization were the current density (3.0, 6.0, and 9.0 mA cm) and flow rate (300 and 3,000 L h). These later values produces laminar and turbulent flow regimes, with Reynolds numbers of 1,100 and 11,000, respectively. None of the four organics contained in the waste is refractory to the photo-electrochemical treatment and they are depleted with the photo-electrolytic technology using large current densities and appropriate electric charge passed. Both direct electrochemical process and mediated anodic oxidation occur during the treatment. First process occurs at turbulent flow condition and low current densities, while the chemical oxidation process happens at laminar flow condition and high current densities. Atrazine and propazine are efficiently removed at laminar flow conditions, with an almost total depletion for the largest current densities. On the contrary, simazine is efficiently removed in turbulent flow conditions and intermediate current density, with removals higher than 90% for 20 kWh m. These results have great significance because they demonstrate the applicability of the electrochemical technology in the treatment of real industrial wastes with a cell specially designed to attain high efficiency in the removal of pollutants.
使用包含尺寸稳定阳极(DSA)和钛作为阴极的中试规模管状流动反应器原型,以恒电流方式对含有阿特拉津、西玛津、羟基三嗪和扑灭通的阿特拉津制造工艺实际废水进行光辅助电化学降解。该废水的主要特征是在所用合成路线中需要大量氯化钠,且按工厂原样使用。工艺优化的变量为电流密度(3.0、6.0和9.0 mA/cm²)和流速(300和3000 L/h)。后两个值分别产生层流和湍流状态,雷诺数分别为1100和11000。废水中所含的四种有机物对光电化学处理均非难降解,并且通过使用大电流密度和通过适当电荷量的光电解技术可将它们去除。处理过程中同时发生直接电化学过程和介导的阳极氧化。第一个过程发生在湍流条件和低电流密度下,而化学氧化过程发生在层流条件和高电流密度下。在层流条件下,阿特拉津和扑灭通能被有效去除,对于最大电流密度几乎可完全去除。相反,西玛津在湍流条件和中等电流密度下能被有效去除,对于20 kWh/m³的去除率高于90%。这些结果具有重要意义,因为它们证明了电化学技术在处理实际工业废水方面的适用性,该电池经过专门设计,可高效去除污染物。