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Comparative degradation studies of Malachite Green and Thiazole Yellow G and their binary mixture using UV/H2O2

机译:使用UV / H2O2比较孔雀石绿和噻唑黄G及其二元混合物的降解研究

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摘要

Wastewater effluents of many industries are usually composed of dye mixtures and their removal poses a significant challenge. The present study reports on the use of an advanced oxidation process namely UV/H2O2 to degrade Malachite Green (MG) (k = 0.0518min(-1)) and Thiazole Yellow G (TYG) (k = 0.0367min(-1)), and their binary mixture in aqueous solutions. Interestingly, it was seen that the photolytic degradation of dyes in binary solution was slower (by 10% for MG and by 46% for TYG) than that in neat solutions under comparable conditions. The total organic carbon analysis (TOC) was also carried out in both the neat dyes (38.5% decrease for MG and 13% decrease for TYG), and in mixture the TOC change was 40%. HPLC analyses confirmed the formation of intermediates in both individual dye solutions, which were however not seen in binary mixtures. The present work shows that dye mixtures behave very differently than neat dyes, and highlights the importance of studying complex dye mixtures and the possible deleterious interactions between dye intermediates during the remediation process.
机译:许多行业的废水通常由染料混合物组成,如何去除废水构成了巨大的挑战。本研究报告了使用高级氧化工艺UV / H2O2降解孔雀石绿(MG)(k = 0.0518min(-1))和噻唑黄G(TYG)(k = 0.0367min(-1)) ,以及它们在水溶液中的二元混合物。有趣的是,在可比较的条件下,发现在二元溶液中染料的光解降解要比纯溶液中的染料光解降解慢(MG降低10%,TYG降低46%)。还对两种纯染料都进行了总有机碳分析(TOC)(MG下降38.5%,TYG下降13%),混合时TOC变化为40%。 HPLC分析证实在两种单独的染料溶液中都形成了中间体,但是在二元混合物中却看不到。目前的工作表明,染料混合物的行为与纯染料完全不同,并且突出了研究复杂的染料混合物以及修复过程中染料中间体之间可能有害的相互作用的重要性。

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