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Membrane fouling and chemical cleaning in water recycling applications

机译:循环水应用中的膜污染和化学清洗

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Fouling and subsequent chemical cleaning are two important issues for sustainable operation of nanofiltration (NF) membranes in water treatment and reuse applications. Fouling strongly depends on the feed water quality, especially the nature of the foulants and ionic composition of the feed water. Consequently, appropriate selection of the chemical cleaning solutions can be seen as a critical factor for effective fouling control. In this study, membrane fouling and chemical cleaning under condition typical to that in water recycling applications were investigated. Fouling conditions were achieved over approximately 18 h with foulant cocktails containing five model foulants namely humic acids, bovine serum albumin, sodium alginate, and two silica colloids in a background electrolyte solution. These model foulants were selected to represent four distinctive modes of fouling: humic acid, protein, polysaccharide, and colloidal fouling. Three chemical cleaning solutions (alkaline solution at pH 11, sodium dodecyl sulphate (SDS), and a combination of both) were evaluated for permeate flux recovery efficiency. The results indicated that with the same mass of foulant, organic fouling was considerably more severe as compared to colloidal fouling. While organic fouling caused a considerable increase in the membrane surface hydrophobicity as indicated by contact angle measurement, hydrophobicity of silica colloidal fouled membrane remained almost the same. Furthermore, a mechanistic correlation amongst cleaning efficiency, characteristics of the model foulants, and the cleaning reagents could be established. Chemical cleaning of all organically fouled membranes by a 10 mM SDS solution particularly at pH 11 resulted in good flux recovery. However, notable flux decline after SDS cleaning of organically fouled membranes was observed indicating that SDS was effective at breaking the organic foulant-Ca~(2+) complex but was not able to effectively dissolve and completely remove these organic foulants. Although a lower permeate flux recovery was obtained with a caustic solution (pH 11) in the absence of SDS, the permeate flux after cleaning was stable. In contrast the chemical cleaning solutions used in this study showed low effectiveness against colloidal fouling. It is also interesting to note that membrane fouling and chemical cleaning could permanently alter the hydrophobicity of the membrane surface.
机译:结垢和随后的化学清洁是纳米过滤(NF)膜在水处理和回用应用中可持续运行的两个重要问题。结垢在很大程度上取决于给水的质量,尤其是结垢的性质和给水的离子组成。因此,正确选择化学清洗液可以被视为有效控制结垢的关键因素。在这项研究中,研究了在水循环应用中典型的条件下的膜污染和化学清洗。在约18小时内,在背景电解质溶液中用含有五种模型污染物的腐质混合物达到了污染条件,所述模型污染物为腐殖酸,牛血清白蛋白,藻酸钠和两种二氧化硅胶体。选择这些模型污垢以代表四种不同的污垢模式:腐殖酸,蛋白质,多糖和胶体污垢。评估了三种化学清洗液(pH值为11的碱性溶液,十二烷基硫酸钠(SDS),以及两者的组合)的渗透通量回收效率。结果表明,与胶体污垢相比,在污垢质量相同的情况下,有机污垢严重得多。如接触角测量所表明的,尽管有机结垢导致膜表面疏水性显着增加,但二氧化硅胶体结垢膜的疏水性几乎保持不变。此外,可以建立清洁效率,模型污垢物的特性和清洁试剂之间的机械关联。用10 mM SDS溶液对所有有机污垢膜进行化学清洗,尤其是在pH 11时,可实现良好的通量回收率。然而,观察到在SDS清洗有机污垢膜后通量显着下降,这表明SDS可以有效地破坏有机污垢-Ca〜(2+)配合物,但不能有效溶解并完全去除这些有机污垢。尽管在没有SDS的情况下使用苛性碱溶液(pH 11)可获得较低的渗透通量回收率,但清洗后的渗透通量是稳定的。相比之下,本研究中使用的化学清洁溶液对胶体结垢的有效性较低。还有趣的是,膜的结垢和化学清洁可永久改变膜表面的疏水性。

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