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Degradation of widespread cyanotoxins with high impact in drinking water (microcystins, cylindrospermopsin, anatoxin-α and saxitoxin) by CWPO

机译:CWPO降解饮用水中影响广泛的蓝藻毒素(微囊藻毒素,环精子藻蛋白,抗毒素α和沙毒素)

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The occurrence of harmful cyanobacterial blooms has unabated increased over the last few decades, posing a significant risk for public health. In this work, we investigate the feasibility of catalytic wet peroxide oxidation (CWPO) promoted by modified natural magnetite (Fe3O4-R400/H2O2), as an inexpensive, simple-operation and environmentally-friendly process for the removal of the cyanotoxins that show the major impact on drinking water: microcystins (MC-LR and MC-RR), cylindrospermopsin (CYN), anatoxin-a (ATX) and saxitoxin (STX). The performance of the system was evaluated under ambient conditions and circumneutral pH (pH(0) = 5) using relevant cyanotoxin concentrations (100-500 mu g L-1). The nature of the cyanotoxins determined their reactivity towards CWPO, which decreased in the following order: MC-RR > CYN > MC-LR ATX > STX. In this sense, microcystins and CYN were completely removed in short reaction times (1-1.5 h) with a low catalyst concentration (0.2 g L-1) and the stoichiometric amount of H2O2 (2-2.6 mg L-1), while only 60-80% conversion was achieved with ADC and STX in 5 h. In these cases, an intensification of the operating conditions (1 g L-1 catalyst and up to 30 mg H2O2 L-1) was required to remove both toxins in 1 h. The impact of the main components of freshwaters i.e. natural organic matter (NOM) and several inorganic ions (HCO3-, HPO42-, SO42-) on the performance of the process was also investigated. Although the former led to a partial inhibition of the reaction due to HO. scavenging and catalyst coating, the latter did not show any remarkably effect, and the versatility of the process was finally confirmed in a real surface water. To further demonstrate the effectiveness of the catalytic system, the toxicity of both the initial cyanotoxins and the resulting CWPO effluents was measured with the brine shrimp Artemia salina. Remarkably, all CWPO effluents were non-toxic at the end of the treatment. (C) 2019 Elsevier Ltd. All rights reserved.
机译:在过去的几十年中,有害的蓝藻水华的发生一直没有减少,对公共健康构成了重大风险。在这项工作中,我们研究了改性天然磁铁矿(Fe3O4-R400 / H2O2)促进的催化湿式过氧化物氧化(CWPO)的可行性,该方法是一种廉价,操作简单且环保的方法,可去除显示出对饮用水的主要影响:微囊藻毒素(MC-LR和MC-RR),环精子藻蛋白(CYN),抗毒素a(ATX)和毒素(STX)。使用相关的氰毒素浓度(100-500μgL-1)在环境条件和周围pH(pH(0)= 5)下评估系统的性能。氰毒素的性质决定了它们对CWPO的反应性,其反应性依次降低:MC-RR> CYN> MC-LR ATX> STX。从这个意义上讲,微囊藻毒素和CYN在较短的反应时间内(1-1.5 h)被完全去除,催化剂浓度低(0.2 g L-1),化学计量的H2O2(2-2.6 mg L-1),而仅在5小时内使用ADC和STX实现了60-80%的转换。在这些情况下,需要加强操作条件(1 g L-1催化剂和最高30 mg H2O2 L-1)以在1小时内除去两种毒素。还研究了淡水的主要成分,即天然有机物(NOM)和几种无机离子(HCO3-,HPO42-,SO42-)对工艺性能的影响。尽管前者由于HO而导致反应的部分抑制。清除和催化剂涂层,后者没有表现出任何明显的作用,并且该方法的多功能性最终在真实的地表水中得到证实。为了进一步证明催化系统的有效性,用卤水虾卤虫盐卤测定了初始氰毒素和所产生的CWPO废水的毒性。值得注意的是,所有CWPO废水在处理结束时都是无毒的。 (C)2019 Elsevier Ltd.保留所有权利。

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