Using nanocomposite materials technology to understand and control reverse osmosis membrane compaction

Citation data:

Desalination, ISSN: 0011-9164, Vol: 261, Issue: 3, Page: 255-263

Publication Year:
2010
Usage 620
Abstract Views 619
Full Text Views 1
Captures 106
Readers 101
Exports-Saves 5
Citations 111
Citation Indexes 111
Repository URL:
http://hdl.handle.net/10754/600153
DOI:
10.1016/j.desal.2010.06.008
Author(s):
Pendergast, Mary Theresa M.; Nygaard, Jodie M.; Ghosh, Asim K.; Hoek, Eric M.V.
Publisher(s):
Elsevier BV
Tags:
Chemistry; Chemical Engineering; Materials Science; Environmental Science; Engineering; Compaction; Desalination; Interfacial polymerization; Nanocomposite; Phase inversion; Reverse osmosis
article description
Composite reverse osmosis (RO) membranes were formed by interfacial polymerization of polyamide thin films over pure polysulfone and nanocomposite-polysulfone support membranes. Nanocomposite support membranes were formed from amorphous non-porous silica and crystalline microporous zeolite nanoparticles. For each hand-cast membrane, water flux and NaCl rejection were monitored over time at two different applied pressures. Nanocomposite-polysulfone supported RO membranes generally had higher initial permeability and experienced less flux decline due to compaction than pure polysulfone supported membranes. In addition, observed salt rejection tended to increase as flux declined from compaction. Cross-sectional SEM images verified significant reduction in thickness of pure polysulfone supports, whereas nanocomposites better resisted compaction due to enhanced mechanical stability imparted by the nanoparticles. A conceptual model was proposed to explain the mechanistic relationship between support membrane compaction and observed changes in water flux and salt rejection. As the support membrane compacts, skin layer pore constriction increased the effective path length for diffusion through the composite membranes, which reduced both water and salt permeability identically. However, experimental salt permeability tended to decline to a greater extent than water permeability; hence, the observed changes in flux and rejection might also be related to structural changes in the polyamide thin film.