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        <identifier>oai:www.ideals.illinois.edu:2142/82456</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_11615</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>McHugh, Anthony J.</dc:contributor>
          <dc:creator>Barton, Benjamin Fredrick</dc:creator>
          <dc:date>2015-09-25T20:44:10Z</dc:date>
          <dc:date>2015-09-25T20:44:10Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1998</dc:date>
          <dc:date>1998</dc:date>
          <dc:description>The Cahn-Hilliard approach is extended to the study of phase separation in ternary polymer/solvent/nonsolvent systems. Three systems are studied: PMMA/N-methyl-2-pyrrolidinone [NMP]/glycerol, for which experimental data are available, and two common membrane-forming systems, poly(ether sulfone) [PES]/dimethylsulfoxide [DMSO]/water and cellulose acetate [CA]/acetone/water. The effects of quench temperature and initial solution composition on the predicted structure-formation dynamics are elucidated. For the PMMA/NMP/glycerol system, model predictions agree well with real-time data obtained from light scattering measurements. Predicted pore growth rate curves exhibit a relative maximum with both quench temperature and nonsolvent composition. For shallow quenches (higher quench temperatures and lower nonsolvent content) near a phase boundary, the pore growth rate increases with increasing quench depth while for deep quenches, where the composition of the polymer rich phase approaches that of a glass, the pore growth rate decreases with increasing quench depth. This behavior seems to be a universal phenomenon in quenched polymer solutions which can undergo a glass transition, and is result of an interplay between thermodynamic and kinetic driving forces for phase separation.</dc:description>
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license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5)
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  Previous issue date: 1998</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 83737
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>152 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1998.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/82456</dc:identifier>
          <dc:identifier>(MiAaPQ)AAI9912189</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:subject>Engineering, Chemical</dc:subject>
          <dc:title>Dynamics of Membrane Structure Formation in Quenched Polymer Solutions</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Chemical Engineering</department>
            <discipline>Chemical Engineering</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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