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        <identifier>oai:www.ideals.illinois.edu:2142/45467</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>Goldbart, Paul M.</dc:contributor>
          <dc:contributor>Stone, Michael</dc:contributor>
          <dc:contributor>Goldbart, Paul M.</dc:contributor>
          <dc:contributor>Abbamonte, Peter M.</dc:contributor>
          <dc:contributor>Weaver, Richard L.</dc:contributor>
          <dc:creator>Rocklin, David Z.</dc:creator>
          <dc:date>2013-08-22T16:41:04Z</dc:date>
          <dc:date>2013-08-22T16:41:04Z</dc:date>
          <dc:date>2013-08</dc:date>
          <dc:date>2013-08-22T16:41:04Z</dc:date>
          <dc:date>2013-08</dc:date>
          <dc:description>The equilibrium statistical mechanics of classical directed polymers in D+1
dimensions is well known to be equivalent to the imaginary-time quantum
dynamics of a quantum many-particle system in D spatial dimensions, with
polymer con gurations corresponding to particle world-lines. This equivalence
motivates the application of techniques originally designed for one-dimensional
many-particle quantum systems to the exploration of many-polymer
systems, as  first recognized and exploited by P.-G. de Gennes [J.
Chem. Phys. 48, 2257 (1968)]. In two dimensions, interactions give rise to
an emergent polymer 
fluid, and I shall examine how topological constraints
on this polymer 
fluid (e.g., due to uncrossable pins or barriers) and their
geometry give rise to strong, entropy-driven forces. I shall also apply quantum
techniques such as Bethe's Ansatz and bosonization to shed light on
the structure of the polymer system. These techniques allow us to examine
how polymer system correlations, thermodynamic properties, and response
to impurities are influenced by strong polymer-polymer interactions.
In three dimensions, polymers wind around one another and polymer topology
may be incorporated via coupling to a Chern-Simons fi eld. As I discuss,
this approach reveals the somewhat reduced role played by interactions in
this higher-dimensional setting, leading to qualitatively diff erent polymer
correlations, thermodynamic properties, and response to impurities.</dc:description>
          <dc:description>Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2013-05-24T21:41:59Z
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University of Illinois Theses &amp; Dissertations (ID: 1)
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          <dc:identifier>http://hdl.handle.net/2142/45467</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2013 David Z. Rocklin</dc:rights>
          <dc:subject>strongly interacting polymer fluids</dc:subject>
          <dc:subject>quantum-classical mapping</dc:subject>
          <dc:title>Directed-polymer systems explored via their quantum analogs</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Physics</department>
            <departmentCode>1244</departmentCode>
            <discipline>Physics</discipline>
            <disciplineCode>0240</disciplineCode>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
            <program>PHD:Physics -UIUC</program>
            <programCode>10KS0240PHD</programCode>
          </degree>
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