Effects of mass retention of dissolved organic matter and membrane pore size on membrane fouling and flux decline

Ultrafiltration (UF) fouling has been attributed to concentration polarization, gel layer formation as well as outer and inner membrane pore clogging. It is believed that mass of humic materials either retained on membrane surface or associated with membrane inner pore surface is the primary cause f...

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Bibliographic Details
Published in:Water research (Oxford) Vol. 43; no. 2; pp. 389 - 394
Main Authors: Lin, Cheng-Fang, Yu-Chen Lin, Angela, Sri Chandana, Panchangam, Tsai, Chao-Yuan
Format: Journal Article
Language:English
Published: Kidlington Elsevier Ltd 01-02-2009
Elsevier
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Summary:Ultrafiltration (UF) fouling has been attributed to concentration polarization, gel layer formation as well as outer and inner membrane pore clogging. It is believed that mass of humic materials either retained on membrane surface or associated with membrane inner pore surface is the primary cause for permeate flux decline and filtration resistance build-up in water supply industries. While biofilm/biofouling and inorganic matter could also be contributing factors for permeability decline in wastewater treatment practices. The present study relates UF fouling to mass of dissolved organic matter (DOM) retained on membrane and quantifies the effect of retained DOM mass on filtration flux decline. The results demonstrate that larger pore membranes exhibit significant flux decline in comparison with the smaller ones. During a 24-h period, dissolved organic carbon mass retained in 10 kDa membranes was about 1.0 g m −2 and that in 100 kDa membranes was more than 3 times higher (3.6 g m −2). The accumulation of retained DOM mass significantly affects permeate flux. It is highly likely that some DOMs bind or aggregate together to form surface gel layer in the smaller 10 kDa UF system; those DOMs largely present in inner pore and serving as pore blockage on a loose membrane (100 kDa) are responsible for severe flux decline.
Bibliography:http://dx.doi.org/10.1016/j.watres.2008.10.042
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ISSN:0043-1354
1879-2448
DOI:10.1016/j.watres.2008.10.042