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Reduced graphene oxide–metal nanoparticle composite membranes for environmental separation and chloro-organic remediation

机译:石墨烯氧化物 - 金属纳米颗粒复合膜进行环境分离和氯有机修复

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This study explores the integration of separation performance of rGO membrane with heterogeneous oxidation reactions for remediation of organic contaminants from water. Herein, an approach was introduced based on layer-by-layer assembly for functionalizing rGO membranes with polyacrylic acid and then by in situ synthesis of Fe based reactive nanoparticles. TEM characterization of the cross-section lamella of the membranes showed a high density of nanoparticles (12% Fe) in the functionalized domain, signifying the importance of polyacrylic acid for in situ synthesis of nanoparticles. The membranes exhibited a pure water permeability of 1.9 LMH bar ~(?1) . The membranes had low to moderate salt retention, and more than 90% neutral red retention (organic probe molecule, size: 1.2 nm). The membranes also exhibited high retention of humic acids (80%), preventing these organics from entering the reactive domain, and thus potentially reducing the formation of undesired by-products. A persulfate mediated oxidative pathway was employed to demonstrate the reactive removal of organic contaminants. The membranes achieved >95% conversion by convectively passing 2 mM persulfate feed at a transmembrane pressure of 0.4 bar. Successful degradation of TCE (up to 61%) was achieved in a single pass by convective flowing of the feed solution through the membrane, generating up to 80% of the theoretical maximum chloride as one of the byproducts. Elevated temperatures significantly enhanced persulfate mediated TCE oxidation extent from 24% at 23 °C to 54% at 40 °C under batch operating conditions.
机译:本研究探讨了RGO膜与异质氧化反应的分离性能的整合,用于修复水中有机污染物。在此,基于逐层组件引入一种方法,用于用聚丙烯酸官能化RGO膜,然后通过原位合成Fe合成的Fe基反应性纳米颗粒。膜的横截面薄片的TEM表征在官能化结构域中显示出高密度的纳米颗粒(12%Fe),从而表示聚丙烯酸对纳米颗粒的原位合成的重要性。膜表现出1.9 LMH条的纯净渗透性〜(?1)。膜具有较低至中度盐保留,且超过90%的中性红色保留(有机探针分子,尺寸:1.2nm)。膜还表现出高保留腐殖酸(80%),防止这些有机物进入反应结构域,因此可能降低了不需要的副产物的形成。使用过硫酸盐介导的氧化途径来证明有机污染物的反应性去除。通过在0.4巴的跨膜压力下对流过2mm过硫酸盐进料来实现> 95%转化率。通过通过膜的对流流动流动进料溶液,在单次通过中成功降解TCE(最多61%),产生高达80%的理论最大氯化物作为副产物之一。升高的温度显着增强过硫酸盐介导的TCE氧化程度在23℃下在批量操作条件下在40℃下在24%至54%。

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