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Role of natural organic matter (NOM), colloidal particles, and solution chemistry on ultrafiltration performance

机译:天然有机物(NOM),胶体颗粒和溶液化学对超滤性能的作用

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摘要

Mechanistic studies on a charged ultrafiltration (UF) membrane fouled with natural organic matter (NOM) and colloidal particles are systematically investigated to understand the relative role of each NOM fraction and the presence of colloidal particulate to membrane fouling. Humic acid (HA), dextran, and kaolin were employed as surrogate model foulants representing the organic hydrophobic acid NOM, hydrophilic neutral NOM, and inorganic colloidal materials, respectively. The results obtained showed that the organic NOM of hydrophilic surrogate (dextran) plays a primary role in promoting membrane fouling, followed by hydrophobic acids and inorganic kaolin, but to a lesser extent than organic NOM compounds. Significant differences in the extent of fouling between dextran and HA have been observed despite filtering with identical membrane. Greater membrane fluxes and better DOC rejection shown by HA could be seen as evidence demonstrating the electrostatic interactions between HA and the negatively charged membrane surface, in addition to the steric hindrance mechanism, despite possessing relatively greater adsorptive interactions with the hydrophobic PSF membrane. These results suggest that NOM structural variations (aromatic versus aliphatic molecular structure), distribution (apparent molecular weight and size), and charge density are essential factors that determine the fouling potential of each NOM fraction. Feed solution containing all the NOM fractions (HA, dextran, and kaolin) fouled the membrane more readily than the individual organic and colloidal foulants, suggesting that an association of the latter two entities is responsible for the greater extent of membrane fouling. Furthermore, the electrokinetic effects of solution chemistry (ionic strength and Ca~(2+)) was employed to quantify the role of electrostatic interactions in providing principal effect that promotes better permeate flux and NOM rejection, particularly with the charged component such as HA. Moreover, observation of this study is beneficial in elucidating a clearer understanding on the influential factors and responsible mechanisms of UF fouling owing to single NOM solute and multiple NOM solute systems, with respect to membrane filterability and rejection efficiency.
机译:系统研究了带电荷的超滤(UF)膜污染了天然有机物质(NOM)和胶体颗粒的机理,以了解每个NOM组分的相对作用以及胶体颗粒的存在对膜污染的影响。腐殖酸(HA),右旋糖酐和高岭土分别用作代表有机疏水酸NOM,亲水性中性NOM和无机胶体材料的替代模型污垢。所得结果表明,亲水性替代物(葡聚糖)的有机NOM在促进膜结垢中起主要作用,其次是疏水性酸和无机高岭土,但程度要小于有机NOM化合物。尽管用相同的膜过滤,但观察到右旋糖酐和HA之间结垢程度的显着差异。 HA表现出的更大的膜通量和更好的DOC截留率可以被视为证明了HA和带负电荷的膜表面之间的静电相互作用(除了空间位阻机理)的证据,尽管与疏水性PSF膜具有相对更大的吸附相互作用。这些结果表明,NOM的结构变化(芳香族与脂肪族分子的结构),分布(表观分子量和大小)以及电荷密度是决定每个NOM组分结垢潜力的重要因素。包含所有NOM馏分(HA,右旋糖酐和高岭土)的进料溶液比单独的有机和胶体污垢物更容易弄脏膜,这表明后两个实体的结合是更大程度的膜污染的原因。此外,采用溶液化学的电动效应(离子强度和Ca〜(2+))来量化静电相互作用的作用,以提供促进更好的渗透通量和NOM排斥的主要作用,尤其是对带电组分(例如HA)。此外,对本研究的观察有助于阐明对单个膜上的NOM和多个膜上的NOM溶质造成的超滤结垢的影响因素和负责任机理的更清晰的理解,以及膜过滤性和截留效率。

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