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首页> 外文期刊>Chemical engineering journal >Integrated treatment of reverse osmosis brines coupling electrocoagulation with advanced oxidation processes
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Integrated treatment of reverse osmosis brines coupling electrocoagulation with advanced oxidation processes

机译:具有先进氧化过程的综合治疗反渗透盐水耦合电凝。

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The potential of integrating electrocoagulation (EleC) with two-stage reverse osmosis (RO) to enhance desalination of secondary/tertiary effluents through removal of dissolved organic matter (DOM) and scaling salts from brines was studied. EleC appears advantageous due to the high electrical conductivity of RO brines and low residual ions concentration. EleC was performed in batch mode in a flow-through cell with recirculation through a stirred reservoir at 9.4 mA/cm~2 current density. Anode was made of Fe or Al as indicated, and cathode of stainless steel. Chemical coagulation (CC) with FeCl3 was tested as reference. EleC resulted in effective removal of phosphate (>99%), carbonate (88-98%) and DOM (40-50%) at a high Faradaic efficiency (>90%). Fe-HeC resulted less suitable than Al-EleC due to partial Fe(H) oxidation at pH 5.5 required for optimal DOM removal, leaving high Fe content and consequently turbidity in the supernatant, whereas residual Al was negligible. At optimal conditions Al release was 75 mg/L for lst-stage brines-ROl (2-fold concentrated) and 300mg/L for 2nd-stage brines-RO2 (-8.3-fold concentrated), corresponding to a specific energy consumption of 0.30 and 0.23 kWh/dm~3/mS/cm Similar results were obtained with CC, however, its main disadvantage was the considerable increase of chlorides in the supernatant. Since coagulation removes quenching components from brines, coupling EleC with advanced oxidation processes (AOP), either UVA/TiO2 or UVC/H2O2, was also evaluated for oxidation of model micropollutants from brines prior to discharge. Either EleC or CC in tandem with AOP increased micropollutants oxidation by 3-4 fold compared to raw brines, achieving practically complete transformation.
机译:通过除去溶解的有机物质(DOM)和从盐水中缩放甲状腺液中,将电凝渗透(ELEC)与两阶段反渗透(RO)相加以增强二次/叔污水的潜水。由于RO盐水和低残留离子浓度的高导电性,ELEC出现有利。在流通电池中以批量模式进行ELEC,通过搅拌贮存器以9.4 mA / cm〜2电流密度进行再循环。阳极由Fe或Al制成,如图所示,也是不锈钢的阴极。用FECL3进行化学凝结(CC)作为参考测试。 ELEC以高法达(> 90%)有效地除去磷酸盐(> 99%),碳酸盐(88-98%)和Dom(40-50%)。由于最佳DOM去除所需的pH5.5所需的pH5.5,留下高Fe含量并因此在上清液中浊度,因此,Fe-HEC导致的al-ELEC不太合适,而残留Al可忽略不计。在最佳条件下,Al释放为75mg / L对于LST-级盐水(2倍浓缩)和300mg / L用于第二阶段盐水-NO2(-8.3倍浓缩),对应于0.30的特定能量消耗和0.23kWh / dm〜3 / ms / mc / cm类似结果用CC获得,然而,其主要缺点是上清液中氯化物的大幅增加。由于凝固从盐水中去除淬火组分,并且还评估了具有晚期氧化过程(AOP)的ELEC,UVA / TiO 2或UVC / H 2 O 2,用于在放电之前从盐水中氧化模型微孔。与原料盐水相比,ELEC或CC串联,通过AOP增加3-4倍,达到3-4倍,实现实际上完全转化。

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