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        <identifier>oai:www.ideals.illinois.edu:2142/49461</identifier>
        <datestamp>2023-07-11</datestamp>
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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>Schroeder, Charles M.</dc:contributor>
          <dc:contributor>Schroeder, Charles M.</dc:contributor>
          <dc:contributor>Higdon, Jonathan J.L.</dc:contributor>
          <dc:contributor>Kenis, Paul J.A.</dc:contributor>
          <dc:contributor>Ewoldt, Randy H.</dc:contributor>
          <dc:creator>Brockman, Christopher A.</dc:creator>
          <dc:date>2014-05-30T16:45:32Z</dc:date>
          <dc:date>2014-05-30T16:45:32Z</dc:date>
          <dc:date>2014-05</dc:date>
          <dc:date>2014-05-30T16:45:32Z</dc:date>
          <dc:date>2014-05</dc:date>
          <dc:description>Polymeric materials play a profound role in our daily lives. There have been many key
advances in polymer processing over the last several decades, but much of the underlying
molecular behavior and physics of polymer solutions is not fully understood. Single molecule
studies of polymer solutions provide an avenue for studying polymer dynamics and can aid in
developing new molecular models of dynamic behavior. For nearly two decades, fluorescentlylabeled
double stranded DNA (dsDNA) has been the model system for studying single molecule
polymer dynamics in non-equilibrium conditions; however, dsDNA is a semiflexible polymer
with markedly different local molecular properties compared to flexible polymer chains, such as
synthetic organic polymers.
This thesis presents a new methodology for studying truly flexible polymers at the single
molecule level. We have demonstrated the ability to synthesize long strands of fluorescentlylabeled
ssDNA, and we directly imaged single ssDNA polymers stretching in fluid flows in
microfluidic devices (Chapter 2). In addition, we have developed an automated flow-based
method to isolate individual polymer chains for long periods of time in planar extensional flow
(Chapter 3). By combining the tools we developed we were able to study the longest polymer
relaxation time dynamics of flexible polymers (Chapter 4), and utilizing both Brownian
dynamics simulations and single molecule experiments, we were able to study the relaxation
dynamics of flexible chains. In addition, we were able to use to automated hydrodynamic trap to
study dynamics of polymers in precisely controlled flow conditions that have not been studied
previously (Chapter 6), as well as the dynamics of a different class of materials: ring polymers.</dc:description>
          <dc:description>Item withdrawn by Laura Spradlin (lspradl2@illinois.edu) on 2014-03-18T13:16:56Z
Item was in collections:
University of Illinois Theses &amp; Dissertations (ID: 1)
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          <dc:identifier>http://hdl.handle.net/2142/49461</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2014 Christopher Brockman</dc:rights>
          <dc:subject>Fluorescence microscopy</dc:subject>
          <dc:subject>polymers</dc:subject>
          <dc:subject>single molecule dynamics</dc:subject>
          <dc:title>Single molecule studies of flexible polymer systems</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Chemical &amp; Biomolecular Engr</department>
            <departmentCode>1687</departmentCode>
            <discipline>Chemical Engineering</discipline>
            <disciplineCode>0300</disciplineCode>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
            <program>PHD:Chemical Engineering -UIUC</program>
            <programCode>10KS0300PHD</programCode>
          </degree>
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