Influence of Surface Pattern Characteristics on Electrolyte Separations Using Charge-Patterned Mosaic Membranes

Doctoral Dissertation


Distinct transport mechanisms emerge when nanostructured substrates are patterned with multiple chemistries. For example, charge-patterned mosaic membranes possess surfaces functionalized with discrete domains of both positive and negative charge. These oppositely-charged domains provide pathways for both the cation and anion from a dissolved salt to permeate through the membrane without violating the macroscopic constraint of electroneutrality. Here, by systematically varying the geometry and size of the charge pattern, we elucidate the molecular interactions that promote the transport of salts under the action of pressure-driven flow. For patterns that consist of equivalent areal coverages of positively-charged and negatively-charged domains, the effects of the geometric parameters were encapsulated in a single variable, the interfacial packing density, that quantified the fraction of the membrane surface covered by junctions between oppositely-charged domains. Experimentally, the transport of symmetric electrolytes (i.e., KCl and MgSO4) increased with the value of the interfacial packing density, while the interfacial packing density did not significantly affect the transport of asymmetric electrolytes (i.e., K2SO4 and MgCl2). Simulations of the electrical potential near the membrane surface demonstrate that for symmetric electrolytes, the structural charge heterogeneity reduces the barrier to ion partitioning thereby promoting salt transport through the membranes. For asymmetric electrolytes, the charge heterogeneity skews the local availability of ions from the stoichiometric ratio of the salt thus hindering salt transport. These findings demonstrate the promise of accessing transport mechanisms which could find utility in a diverse range of chemical separations and sensing applications through chemical-patterning of membranes.


Attribute NameValues
Author Feng Gao
Contributor William A. Phillip, Research Director
Degree Level Doctoral Dissertation
Degree Discipline Chemical and Biomolecular Engineering
Degree Name Doctor of Philosophy
Banner Code

Defense Date
  • 2020-01-31

Submission Date 2020-03-07
Record Visibility Public
Content License
  • All rights reserved

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