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contributor authorAnne Braghetta
contributor authorFrancis A. DiGiano
contributor authorWilliam P. Ball
date accessioned2017-05-08T21:21:03Z
date available2017-05-08T21:21:03Z
date copyrightJuly 1997
date issued1997
identifier other%28asce%290733-9372%281997%29123%3A7%28628%29.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/48031
description abstractStudies were conducted to examine the effect of solution chemistry, defined here as pH and ionic strength, on the permeability of negatively charged polymeric nanofiltration membranes. Water permeation through the membrane was demonstrated to decrease at conditions of low pH and high ionic strength in the absence of organic macromolecules. The reduction in membrane permeability was attributed to a compaction of the membrane matrix resulting from charge neutralization at the membrane surface and electric double layer compression. An uncharged model organic macromolecule (polyethylene glycol) was used to quantify the effects of solution chemistry on membrane compaction and solute rejection capabilities of the charged membrane. Studies of membrane permeability and rejection were then repeated with solutions containing natural organic matter (NOM), enabling concurrent evaluation of the effects of electric double layer compression as well as changes in both membrane structure and the apparent macromolecular size of charged NOM macromolecules.
publisherAmerican Society of Civil Engineers
titleNanofiltration of Natural Organic Matter: pH and Ionic Strength Effects
typeJournal Paper
journal volume123
journal issue7
journal titleJournal of Environmental Engineering
identifier doi10.1061/(ASCE)0733-9372(1997)123:7(628)
treeJournal of Environmental Engineering:;1997:;Volume ( 123 ):;issue: 007
contenttypeFulltext


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