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        <identifier>oai:www.ideals.illinois.edu:2142/82443</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, A.J.</dc:contributor>
          <dc:creator>Immaneni, Aravind</dc:creator>
          <dc:date>2015-09-25T20:44:05Z</dc:date>
          <dc:date>2015-09-25T20:44:05Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1997</dc:date>
          <dc:date>1997</dc:date>
          <dc:description>"The third study involves the conformational and phase stability of aqueous Poly-L-Lysine solutions in shear flow. Poly-L-lysine exists as an $\alpha$-helix at high pH and a random coil at neutral pH. When the $\alpha$-helix is heated above 27$\sp\circ$C, the macromolecule undergoes a conformational transition to a $\beta$-sheet. In this study, the stability of the secondary structure of poly-L-lysine in solutions subjected to shear flow, at temperatures below the $\alpha$-helix to $\beta$-sheet transition temperature, were examined using Raman spectroscopy and circular dichroism (CD). Solutions initially in the $\alpha$-helical state showed time-dependent increases in viscosity with shearing, rising to values as much as an order of magnitude. Visual observation and turbidity measurements showed the formation of a gel like phase under flow. Laser Raman measurements demonstrated the presence of small amounts of $\beta$-sheet structure evidenced by the amide I band at 1666 cm$\sp{-1}$. CD measurements indicated that solutions of predominantly $\alpha$-helical conformation at 20$\sp\circ$C transformed into 85% $\alpha$-helix and 15% $\beta$-sheet after being sheared for 20 minutes. However, on continued shearing the content of $\beta$-sheet conformation decreased. The observed phenomena were explained in terms of a ""zipping up"" molecular model based on flow enhanced hydrophobic interactions similar to that observed in gel-forming flexible polymers. (Abstract shortened by UMI.)."</dc:description>
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  Previous issue date: 1997</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 83724
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>140 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1997.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/82443</dc:identifier>
          <dc:identifier>(MiAaPQ)AAI9812639</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:subject>Engineering, Chemical</dc:subject>
          <dc:title>Conformational and Orientational Dynamics of Semi-Rigid Macromolecules in Shear Flow</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>
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