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NAMS 2002 Workshop - ICOM 2008

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Hybrid and Novel Processes II – 2<br />

Thursday July 17, 3:00 PM-3:30 PM, Kaua’i<br />

Nanoparticle-Enhanced Microfiltration for Low Energy Metal Removal from<br />

Water.<br />

A. Jawor (Speaker), University Of California Los Angeles, Los Angeles, California, USA -<br />

ajawor@ucla.edu<br />

E. Hoek, University Of California Los Angeles, Los Angeles, California, USA<br />

Polymer-enhanced ultrafiltration (PEUF) is highly effective for selectively<br />

removing metal ions from water, but this process is difficult to implement in<br />

practice because polymer gel formation and pore plugging lead to severe, often<br />

irreversible flux decline. Recently, dendritic polymers (a.k.a., dendrimers) have<br />

been proposed as a high-binding capacity, low-fouling alternative to traditional<br />

polyelectrolytes. However, dendrimers are very expensive and require use of<br />

tight, ultrafiltration membranes. Nanoparticle-enhanced microfiltration (NEMF) is<br />

a hybrid membrane process, like PEUF, where a target contaminant selectively<br />

reacts with nanoparticles added to a mixed reactor. Contaminant-nanoparticle<br />

complexes are removed using low-pressure microfiltration membranes.<br />

In this study, we evaluate nanoparticle-enhanced microfiltration using inorganic<br />

nanoparticles. Our objective is to demonstrate selective removal of divalent metal<br />

cations from simple and complex electrolytes through addition of metal-binding<br />

nanoparticles followed by microfiltration. As a first step towards testing this<br />

concept, we evaluate a traditional polyelectrolyte (polyacrylic acid), a succinic<br />

and carboxylic acid functionalized PAMAM dendrimers, and a NaA zeolite<br />

nanocrystals as metal-binding agents in combination with various microfiltration<br />

and ultrafiltration membranes. Electron microscopy, light scattering, particle<br />

electrophoresis, direct titrations, and contact angle analyses are used to<br />

characterize nanoparticle size, shape, hydrodynamic radius, zeta potential,<br />

charge density, and surface energy, respectively. Preliminary metal-binding<br />

experiments are performed to elucidate nanoparticle binding kinetics, capacity<br />

and strength (i.e., reversibility) using various divalent metal ions (Ca 2+ , Mg 2+ ,<br />

Ba 2+ , Sr 2+ , Cd 2+ ). Nanoparticle rejections and flux decline are determined using<br />

polysulfone- based UF and MF membranes ranging from molecular weight cut-off<br />

(MWCO) of 5 kD up to a characteristic pore size of 100 nm. Mechanisms of<br />

membrane fouling by polymers, dendrimers, and nanocrystals are elucidated by<br />

fitting flux decline data with classical blocking filtration models. Clean and fouled<br />

membrane surfaces are analyzed by SEM/EDX to confirm morphology and<br />

composition of fouling layers formed. Additional membrane characterization<br />

includes pure water permeability and zeta potential by electrolyte filtration<br />

experiments, plus surface roughness and energy via AFM and contact angle<br />

analyses.

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