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    <title>PRE: Polymers</title>
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    <description>Recently published articles in Phys. Rev. E in the Table of Content section "Polymers"</description>
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    <syn:updateBase>2012-02-10T21:05:31-05:00</syn:updateBase>
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    <dc:date>2012-02-10T21:05:31-05:00</dc:date>
    <dc:language>en</dc:language>
    <dc:rights>Copyright © 2012 the American Physical Society. Personal use only, all commercial or other reuse prohibited</dc:rights>
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  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.85.021802">
    <title>Slow knot formation by suppressed self-reptation in a collapsed polymer chain</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.85.021802</link>
    <description>Author(s): Mitsuo Nakata, Yoshiki Nakamura, Naoki Sasaki, and Yasuyuki Maki&lt;br/&gt;&lt;p&gt;Chain-expansion processes from knotted globules have been measured for poly(methyl methacrylate) (PMMA) in the mixed solvent tert-butyl alcohol (TBA) &lt;span&gt;+&lt;/span&gt; water (2.5 vol &lt;span&gt;%&lt;/span&gt;) by static light scattering. The solution was quenched from the &lt;span&gt;&lt;span style="font-style: italic;"&gt;Θ&lt;/span&gt;&lt;/span&gt; temperature of 41.5 &lt;span&gt;&lt;sup&gt;∘&lt;/sup&gt;&lt;/span&gt;C to 37.0 &lt;span&gt;&lt;sup&gt;∘&lt;/sup&gt;&lt;/span&gt;C, aged there for a time period &lt;span&gt;&lt;span style="font-style: italic;"&gt;t&lt;/span&gt;&lt;sub&gt;...&lt;/sub&gt;&lt;/span&gt;&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 85, 021802] Published Fri Feb 10, 2012</description>
    <content:encoded><![CDATA[<p>Author(s): Mitsuo Nakata, Yoshiki Nakamura, Naoki Sasaki, and Yasuyuki Maki</p><p> Chain-expansion processes from knotted globules have been measured for poly(methyl methacrylate) (PMMA) in the mixed solvent tert-butyl alcohol (TBA) <span>+</span> water (2.5 vol <span>%</span>) by static light scattering. The solution was quenched from the <span><span style="font-style: italic;">Θ</span></span> temperature of 41.5 <span><sup>∘</sup></span>C to 37.0 <span><sup>∘</sup></span>C, aged there for a time period <span><span style="font-style: italic;">t</span><sub>...</sub></span></p><p>[Phys. Rev. E 85, 021802] Published Fri Feb 10, 2012</p>]]></content:encoded>
    <dc:title>Slow knot formation by suppressed self-reptation in a collapsed polymer chain</dc:title>
    <dc:creator>Mitsuo Nakata, Yoshiki Nakamura, Naoki Sasaki, and Yasuyuki Maki</dc:creator>
    <dc:date>2012-02-10T10:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.85.021802</dc:identifier>
    <dc:source>Phys. Rev. E 85, 021802 (2012)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>85</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2012-02-10T10:00:00-05:00</prism:publicationDate>
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    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.85.021802</prism:url>
    <prism:startingPage>021802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.85.021801">
    <title>Nonlinear effective-medium theory of disordered spring networks</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.85.021801</link>
    <description>Author(s): M. Sheinman, C. P. Broedersz, and F. C. MacKintosh&lt;br/&gt;&lt;p&gt;Disordered soft materials, such as fibrous networks in biological contexts, exhibit a nonlinear elastic response. We study such nonlinear behavior with a minimal model for networks on lattice geometries with simple Hookian elements with disordered spring constant. By developing a mean-field approach...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 85, 021801] Published Wed Feb 08, 2012</description>
    <content:encoded><![CDATA[<p>Author(s): M. Sheinman, C. P. Broedersz, and F. C. MacKintosh</p><p> Disordered soft materials, such as fibrous networks in biological contexts, exhibit a nonlinear elastic response. We study such nonlinear behavior with a minimal model for networks on lattice geometries with simple Hookian elements with disordered spring constant. By developing a mean-field approach...</p><p>[Phys. Rev. E 85, 021801] Published Wed Feb 08, 2012</p>]]></content:encoded>
    <dc:title>Nonlinear effective-medium theory of disordered spring networks</dc:title>
    <dc:creator>M. Sheinman, C. P. Broedersz, and F. C. MacKintosh</dc:creator>
    <dc:date>2012-02-08T10:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.85.021801</dc:identifier>
    <dc:source>Phys. Rev. E 85, 021801 (2012)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>85</prism:volume>
    <prism:number>2</prism:number>
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    <prism:startingPage>021801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.85.011801">
    <title>Comparison of the kinetic friction of planar neutral and polyelectrolyte polymer brushes using molecular dynamics simulations</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.85.011801</link>
    <description>Author(s): Yangpeng Ou, Jeffrey B. Sokoloff, and Mark J. Stevens&lt;br/&gt;&lt;p&gt;We have simulated the relative shear motion of both neutral and polyelectrolyte end-grafted polymer brushes using molecular dynamics. The flexible neutral polymer brush is treated as a bead-spring model, and the polyelectrolyte brush is treated the same way except that each bead is charged and there...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 85, 011801] Published Fri Jan 06, 2012</description>
    <content:encoded><![CDATA[<p>Author(s): Yangpeng Ou, Jeffrey B. Sokoloff, and Mark J. Stevens</p><p> We have simulated the relative shear motion of both neutral and polyelectrolyte end-grafted polymer brushes using molecular dynamics. The flexible neutral polymer brush is treated as a bead-spring model, and the polyelectrolyte brush is treated the same way except that each bead is charged and there...</p><p>[Phys. Rev. E 85, 011801] Published Fri Jan 06, 2012</p>]]></content:encoded>
    <dc:title>Comparison of the kinetic friction of planar neutral and polyelectrolyte polymer brushes using molecular dynamics simulations</dc:title>
    <dc:creator>Yangpeng Ou, Jeffrey B. Sokoloff, and Mark J. Stevens</dc:creator>
    <dc:date>2012-01-06T10:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.85.011801</dc:identifier>
    <dc:source>Phys. Rev. E 85, 011801 (2012)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>85</prism:volume>
    <prism:number>1</prism:number>
    <prism:publicationDate>2012-01-06T10:00:00-05:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.85.011801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.85.011801</prism:url>
    <prism:startingPage>011801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.061801">
    <title>Aggregation kinetics of a simulated telechelic polymer</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.061801</link>
    <description>Author(s): Mark Wilson, Avinoam Rabinovitch, and Arlette R. C. Baljon&lt;br/&gt;&lt;p&gt;We investigate the aggregation kinetics of a simulated telechelic polymer gel. In the hybrid molecular dynamics (MD)/Monte Carlo (MC) algorithm, aggregates of associating end groups form and break according to MC rules, while the position of the polymers in space is dictated by MD. As a result, the ...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 061801] Published Mon Dec 05, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Mark Wilson, Avinoam Rabinovitch, and Arlette R. C. Baljon</p><p> We investigate the aggregation kinetics of a simulated telechelic polymer gel. In the hybrid molecular dynamics (MD)/Monte Carlo (MC) algorithm, aggregates of associating end groups form and break according to MC rules, while the position of the polymers in space is dictated by MD. As a result, the ...</p><p>[Phys. Rev. E 84, 061801] Published Mon Dec 05, 2011</p>]]></content:encoded>
    <dc:title>Aggregation kinetics of a simulated telechelic polymer</dc:title>
    <dc:creator>Mark Wilson, Avinoam Rabinovitch, and Arlette R. C. Baljon</dc:creator>
    <dc:date>2011-12-05T10:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.061801</dc:identifier>
    <dc:source>Phys. Rev. E 84, 061801 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>6</prism:number>
    <prism:publicationDate>2011-12-05T10:00:00-05:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.061801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.061801</prism:url>
    <prism:startingPage>061801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.051805">
    <title>Simulating flexible polymers in a potential of randomly distributed hard disks</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.051805</link>
    <description>Author(s): Sebastian Schöbl, Johannes Zierenberg, and Wolfhard Janke&lt;br/&gt;&lt;p&gt;We perform equilibrium computer simulations of a two-dimensional pinned flexible polymer exposed to a quenched disorder potential consisting of hard disks. We are especially interested in the high-density regime of the disorder, where subtle structures such as cavities and channels play a central ro...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 051805] Published Mon Nov 28, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Sebastian Schöbl, Johannes Zierenberg, and Wolfhard Janke</p><p> We perform equilibrium computer simulations of a two-dimensional pinned flexible polymer exposed to a quenched disorder potential consisting of hard disks. We are especially interested in the high-density regime of the disorder, where subtle structures such as cavities and channels play a central ro...</p><p>[Phys. Rev. E 84, 051805] Published Mon Nov 28, 2011</p>]]></content:encoded>
    <dc:title>Simulating flexible polymers in a potential of randomly distributed hard disks</dc:title>
    <dc:creator>Sebastian Schöbl, Johannes Zierenberg, and Wolfhard Janke</dc:creator>
    <dc:date>2011-11-28T10:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.051805</dc:identifier>
    <dc:source>Phys. Rev. E 84, 051805 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>5</prism:number>
    <prism:publicationDate>2011-11-28T10:00:00-05:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.051805</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.051805</prism:url>
    <prism:startingPage>051805</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.051804">
    <title>Numerical simulation methods for the Rouse model in flow</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.051804</link>
    <description>Author(s): Michael P. Howard and Scott T. Milner&lt;br/&gt;&lt;p&gt;Simulation of the Rouse model in flow underlies a great variety of numerical investigations of polymer dynamics, in both entangled melts and solutions and in dilute solution. Typically a simple explicit stochastic Euler method is used to evolve the Rouse model. Here we compare this approach to an op...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 051804] Published Mon Nov 28, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Michael P. Howard and Scott T. Milner</p><p> Simulation of the Rouse model in flow underlies a great variety of numerical investigations of polymer dynamics, in both entangled melts and solutions and in dilute solution. Typically a simple explicit stochastic Euler method is used to evolve the Rouse model. Here we compare this approach to an op...</p><p>[Phys. Rev. E 84, 051804] Published Mon Nov 28, 2011</p>]]></content:encoded>
    <dc:title>Numerical simulation methods for the Rouse model in flow</dc:title>
    <dc:creator>Michael P. Howard and Scott T. Milner</dc:creator>
    <dc:date>2011-11-28T10:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.051804</dc:identifier>
    <dc:source>Phys. Rev. E 84, 051804 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>5</prism:number>
    <prism:publicationDate>2011-11-28T10:00:00-05:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.051804</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.051804</prism:url>
    <prism:startingPage>051804</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.051803">
    <title>Measurement of the skin layer in the drying process of a polymer solution</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.051803</link>
    <description>Author(s): Yuji Shimokawa, Tadashi Kajiya, Keiji Sakai, and Masao Doi&lt;br/&gt;&lt;p&gt;When a polymer solution is dried in air, a polymer-concentrated region, called a “skin” layer, often appears near the surface. In this paper, an experimental method is proposed for detecting the initial process of the formation of the skin layer. An electric field is applied on the surface of polyme...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 051803] Published Fri Nov 04, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Yuji Shimokawa, Tadashi Kajiya, Keiji Sakai, and Masao Doi</p><p> When a polymer solution is dried in air, a polymer-concentrated region, called a “skin” layer, often appears near the surface. In this paper, an experimental method is proposed for detecting the initial process of the formation of the skin layer. An electric field is applied on the surface of polyme...</p><p>[Phys. Rev. E 84, 051803] Published Fri Nov 04, 2011</p>]]></content:encoded>
    <dc:title>Measurement of the skin layer in the drying process of a polymer solution</dc:title>
    <dc:creator>Yuji Shimokawa, Tadashi Kajiya, Keiji Sakai, and Masao Doi</dc:creator>
    <dc:date>2011-11-04T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.051803</dc:identifier>
    <dc:source>Phys. Rev. E 84, 051803 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>5</prism:number>
    <prism:publicationDate>2011-11-04T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.051803</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.051803</prism:url>
    <prism:startingPage>051803</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.051802">
    <title>Charge carrier dynamics and relaxation in (polyethylene oxide-lithium-salt)-based polymer electrolyte containing 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide as ionic liquid</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.051802</link>
    <description>Author(s): A. Karmakar and A. Ghosh&lt;br/&gt;&lt;p&gt;In this paper we report the dynamics of charge carriers and relaxation in polymer electrolytes based on polyethylene oxide (PEO), lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMPTFSI) ionic liquid prepared by solution cast te...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 051802] Published Wed Nov 02, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): A. Karmakar and A. Ghosh</p><p> In this paper we report the dynamics of charge carriers and relaxation in polymer electrolytes based on polyethylene oxide (PEO), lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMPTFSI) ionic liquid prepared by solution cast te...</p><p>[Phys. Rev. E 84, 051802] Published Wed Nov 02, 2011</p>]]></content:encoded>
    <dc:title>Charge carrier dynamics and relaxation in (polyethylene oxide-lithium-salt)-based polymer electrolyte containing 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide as ionic liquid</dc:title>
    <dc:creator>A. Karmakar and A. Ghosh</dc:creator>
    <dc:date>2011-11-02T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.051802</dc:identifier>
    <dc:source>Phys. Rev. E 84, 051802 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>5</prism:number>
    <prism:publicationDate>2011-11-02T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.051802</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.051802</prism:url>
    <prism:startingPage>051802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.051801">
    <title>Tube-width fluctuations of entangled stiff polymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.051801</link>
    <description>Author(s): Jens Glaser and Klaus Kroy&lt;br/&gt;&lt;p&gt;The tubelike cages of stiff polymers in entangled solutions have been shown to exhibit characteristic spatial heterogeneities. We explain these observations by a systematic theory generalizing previous work by Morse [ &lt;a href="http://dx.doi.org/10.1103/PhysRevE.63.031502"&gt; Phys. Rev. E &lt;span style="font-weight: bold;"&gt;63&lt;/span&gt; 031502 (2001)&lt;/a&gt;]. With a local version of the binary collision appr...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 051801] Published Tue Nov 01, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Jens Glaser and Klaus Kroy</p><p> The tubelike cages of stiff polymers in entangled solutions have been shown to exhibit characteristic spatial heterogeneities. We explain these observations by a systematic theory generalizing previous work by Morse [ <a href="http://dx.doi.org/10.1103/PhysRevE.63.031502"> Phys. Rev. E <span style="font-weight: bold;">63</span> 031502 (2001)</a>]. With a local version of the binary collision appr...</p><p>[Phys. Rev. E 84, 051801] Published Tue Nov 01, 2011</p>]]></content:encoded>
    <dc:title>Tube-width fluctuations of entangled stiff polymers</dc:title>
    <dc:creator>Jens Glaser and Klaus Kroy</dc:creator>
    <dc:date>2011-11-01T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.051801</dc:identifier>
    <dc:source>Phys. Rev. E 84, 051801 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>5</prism:number>
    <prism:publicationDate>2011-11-01T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.051801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.051801</prism:url>
    <prism:startingPage>051801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041810">
    <title>Orientational ordering transitions of semiflexible polymers in thin films: A Monte Carlo simulation</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041810</link>
    <description>Author(s): V. A. Ivanov, A. S. Rodionova, E. A. An, J. A. Martemyanova, M. R. Stukan, M. Müller, W. Paul, and K. Binder&lt;br/&gt;&lt;p&gt;Athermal solutions (from dilute to concentrated) of semiflexible macromolecules confined in a film of thickness &lt;span&gt;&lt;span style="font-style: italic;"&gt;D&lt;/span&gt;&lt;/span&gt; between two hard walls are studied by means of grand-canonical lattice Monte Carlo simulation using the bond fluctuation model. This system exhibits two phase transitions as a function o...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041810] Published Fri Oct 28, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): V. A. Ivanov, A. S. Rodionova, E. A. An, J. A. Martemyanova, M. R. Stukan, M. Müller, W. Paul, and K. Binder</p><p> Athermal solutions (from dilute to concentrated) of semiflexible macromolecules confined in a film of thickness <span><span style="font-style: italic;">D</span></span> between two hard walls are studied by means of grand-canonical lattice Monte Carlo simulation using the bond fluctuation model. This system exhibits two phase transitions as a function o...</p><p>[Phys. Rev. E 84, 041810] Published Fri Oct 28, 2011</p>]]></content:encoded>
    <dc:title>Orientational ordering transitions of semiflexible polymers in thin films: A Monte Carlo simulation</dc:title>
    <dc:creator>V. A. Ivanov, A. S. Rodionova, E. A. An, J. A. Martemyanova, M. R. Stukan, M. Müller, W. Paul, and K. Binder</dc:creator>
    <dc:date>2011-10-28T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041810</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041810 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-28T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041810</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041810</prism:url>
    <prism:startingPage>041810</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041809">
    <title>Coil-bridge transition and Monte Carlo simulation of a stretched polymer</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041809</link>
    <description>Author(s): Jeff Z. Y. Chen&lt;br/&gt;&lt;p&gt;The structure of the system consisting of a grafted self-avoiding polymer chain attracted to the surface layer of a flat wall at a distance away by a short-ranged force is investigated. A first-order transition is determined between the coil state at a low attraction energy and the bridge state at a...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041809] Published Tue Oct 25, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Jeff Z. Y. Chen</p><p> The structure of the system consisting of a grafted self-avoiding polymer chain attracted to the surface layer of a flat wall at a distance away by a short-ranged force is investigated. A first-order transition is determined between the coil state at a low attraction energy and the bridge state at a...</p><p>[Phys. Rev. E 84, 041809] Published Tue Oct 25, 2011</p>]]></content:encoded>
    <dc:title>Coil-bridge transition and Monte Carlo simulation of a stretched polymer</dc:title>
    <dc:creator>Jeff Z. Y. Chen</dc:creator>
    <dc:date>2011-10-25T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041809</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041809 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-25T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041809</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041809</prism:url>
    <prism:startingPage>041809</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041808">
    <title>Glass transition dynamics of stacked thin polymer films</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041808</link>
    <description>Author(s): Koji Fukao, Takehide Terasawa, Yuto Oda, Kenji Nakamura, and Daisuke Tahara&lt;br/&gt;&lt;p&gt;The glass transition dynamics of stacked thin films of polystyrene and poly(2-chlorostyrene) were investigated using differential scanning calorimetry and dielectric relaxation spectroscopy. The glass transition temperature &lt;span&gt;&lt;span style="font-style: italic;"&gt;T&lt;/span&gt;&lt;sub&gt;&lt;span style="font-style: italic;"&gt;g&lt;/span&gt;&lt;/sub&gt;&lt;/span&gt; of as-stacked thin polystyrene films has a strong depression from that of...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041808] Published Mon Oct 24, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Koji Fukao, Takehide Terasawa, Yuto Oda, Kenji Nakamura, and Daisuke Tahara</p><p> The glass transition dynamics of stacked thin films of polystyrene and poly(2-chlorostyrene) were investigated using differential scanning calorimetry and dielectric relaxation spectroscopy. The glass transition temperature <span><span style="font-style: italic;">T</span><sub><span style="font-style: italic;">g</span></sub></span> of as-stacked thin polystyrene films has a strong depression from that of...</p><p>[Phys. Rev. E 84, 041808] Published Mon Oct 24, 2011</p>]]></content:encoded>
    <dc:title>Glass transition dynamics of stacked thin polymer films</dc:title>
    <dc:creator>Koji Fukao, Takehide Terasawa, Yuto Oda, Kenji Nakamura, and Daisuke Tahara</dc:creator>
    <dc:date>2011-10-24T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041808</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041808 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-24T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041808</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041808</prism:url>
    <prism:startingPage>041808</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041807">
    <title>Self-assembly of (A-comb-C)-b-(B-comb-C) diblock copolymer-based comb copolymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041807</link>
    <description>Author(s): V. Markov, A. Subbotin, and G. ten Brinke&lt;br/&gt;&lt;p&gt;The phase behavior of (&lt;span&gt;&lt;span style="font-style: italic;"&gt;A&lt;/span&gt;&lt;/span&gt;-comb-&lt;span&gt;&lt;span style="font-style: italic;"&gt;C&lt;/span&gt;&lt;/span&gt;)-&lt;span&gt;&lt;span style="font-style: italic;"&gt;b&lt;/span&gt;&lt;/span&gt;-(&lt;span&gt;&lt;span style="font-style: italic;"&gt;B&lt;/span&gt;&lt;/span&gt;-comb-&lt;span&gt;&lt;span style="font-style: italic;"&gt;C&lt;/span&gt;&lt;/span&gt;) diblock copolymer melts is investigated using the strong segregation theory approach. Three different regimes are distinguished. In regime 1 both disordered comb blocks are microphase separated from each other, in regime 2 the side chains &lt;span&gt;&lt;span style="font-style: italic;"&gt;C&lt;/span&gt;&lt;/span&gt; are microphas...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041807] Published Thu Oct 20, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): V. Markov, A. Subbotin, and G. ten Brinke</p><p> The phase behavior of (<span><span style="font-style: italic;">A</span></span>-comb-<span><span style="font-style: italic;">C</span></span>)-<span><span style="font-style: italic;">b</span></span>-(<span><span style="font-style: italic;">B</span></span>-comb-<span><span style="font-style: italic;">C</span></span>) diblock copolymer melts is investigated using the strong segregation theory approach. Three different regimes are distinguished. In regime 1 both disordered comb blocks are microphase separated from each other, in regime 2 the side chains <span><span style="font-style: italic;">C</span></span> are microphas...</p><p>[Phys. Rev. E 84, 041807] Published Thu Oct 20, 2011</p>]]></content:encoded>
    <dc:title>Self-assembly of (A-comb-C)-b-(B-comb-C) diblock copolymer-based comb copolymers</dc:title>
    <dc:creator>V. Markov, A. Subbotin, and G. ten Brinke</dc:creator>
    <dc:date>2011-10-20T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041807</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041807 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-20T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041807</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041807</prism:url>
    <prism:startingPage>041807</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041806">
    <title>Polymer dynamics in semidilute solution during electrospinning: A simple model and experimental observations</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041806</link>
    <description>Author(s): Israel Greenfeld, Arkadii Arinstein, Kamel Fezzaa, Miriam H. Rafailovich, and Eyal Zussman&lt;br/&gt;&lt;p&gt;Electrospun polymer nanofibers demonstrate outstanding mechanical and thermodynamic properties as compared to macroscopic-scale structures. Our previous work has demonstrated that these features are attributed to nanofiber microstructure [ &lt;a href="http://dx.doi.org/10.1038/nnano.2006.172"&gt; Nat. Nanotechnol. &lt;span style="font-weight: bold;"&gt;2&lt;/span&gt; 59 (2007)&lt;/a&gt;]. It is clear that this micro...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041806] Published Fri Oct 14, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Israel Greenfeld, Arkadii Arinstein, Kamel Fezzaa, Miriam H. Rafailovich, and Eyal Zussman</p><p> Electrospun polymer nanofibers demonstrate outstanding mechanical and thermodynamic properties as compared to macroscopic-scale structures. Our previous work has demonstrated that these features are attributed to nanofiber microstructure [ <a href="http://dx.doi.org/10.1038/nnano.2006.172"> Nat. Nanotechnol. <span style="font-weight: bold;">2</span> 59 (2007)</a>]. It is clear that this micro...</p><p>[Phys. Rev. E 84, 041806] Published Fri Oct 14, 2011</p>]]></content:encoded>
    <dc:title>Polymer dynamics in semidilute solution during electrospinning: A simple model and experimental observations</dc:title>
    <dc:creator>Israel Greenfeld, Arkadii Arinstein, Kamel Fezzaa, Miriam H. Rafailovich, and Eyal Zussman</dc:creator>
    <dc:date>2011-10-14T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041806</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041806 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-14T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041806</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041806</prism:url>
    <prism:startingPage>041806</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041805">
    <title>Viscosity measurements of thin polymer films from reflow of spatially modulated nanoimprinted patterns</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041805</link>
    <description>Author(s): Etienne Rognin, Stefan Landis, and Laurent Davoust&lt;br/&gt;&lt;p&gt;We present a method to measure the viscosity of polymer thin films. The material is spin coated onto a silicon substrate and specially designed nanopatterns are imprinted on the film using thermal nanoimprint. A brief reflow is performed during which patterns flow under surface tension. Spectral den...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041805] Published Fri Oct 14, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Etienne Rognin, Stefan Landis, and Laurent Davoust</p><p> We present a method to measure the viscosity of polymer thin films. The material is spin coated onto a silicon substrate and specially designed nanopatterns are imprinted on the film using thermal nanoimprint. A brief reflow is performed during which patterns flow under surface tension. Spectral den...</p><p>[Phys. Rev. E 84, 041805] Published Fri Oct 14, 2011</p>]]></content:encoded>
    <dc:title>Viscosity measurements of thin polymer films from reflow of spatially modulated nanoimprinted patterns</dc:title>
    <dc:creator>Etienne Rognin, Stefan Landis, and Laurent Davoust</dc:creator>
    <dc:date>2011-10-14T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041805</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041805 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-14T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041805</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041805</prism:url>
    <prism:startingPage>041805</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041804">
    <title>Theory of the polyelectrolyte dielectric function</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041804</link>
    <description>Author(s): C.-Y. David Lu&lt;br/&gt;&lt;p&gt;A simple double-layer polarization theory is developed for the flexible polyelectrolyte solution. Under the applied electric field, the double layer of the polyelectrolyte induces the excess line fluxes of charge and salt within the double layer. The off-diagonal Onsager coefficient couples the char...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041804] Published Thu Oct 13, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): C.-Y. David Lu</p><p> A simple double-layer polarization theory is developed for the flexible polyelectrolyte solution. Under the applied electric field, the double layer of the polyelectrolyte induces the excess line fluxes of charge and salt within the double layer. The off-diagonal Onsager coefficient couples the char...</p><p>[Phys. Rev. E 84, 041804] Published Thu Oct 13, 2011</p>]]></content:encoded>
    <dc:title>Theory of the polyelectrolyte dielectric function</dc:title>
    <dc:creator>C.-Y. David Lu</dc:creator>
    <dc:date>2011-10-13T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041804</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041804 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-13T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041804</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041804</prism:url>
    <prism:startingPage>041804</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041803">
    <title>Dependence of the disorder-lamellar stability boundary of a melt of asymmetric wormlike AB diblock copolymers on the chain rigidity</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041803</link>
    <description>Author(s): Ying Jiang, Wu-Yang Zhang, and Jeff Z. Y. Chen&lt;br/&gt;&lt;p&gt;We study the disorder-order transition boundary of wormlile &lt;span&gt;&lt;span style="font-style: italic;"&gt;A&lt;/span&gt;&lt;span style="font-style: italic;"&gt;B&lt;/span&gt;&lt;/span&gt; diblock copolymers on the basis of the wormlike chain formalism aided by a self-consistent mean-field treatment. We examine the influence of the persistency on the phase diagram and properties of the phase transition as a function of the...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041803] Published Thu Oct 13, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Ying Jiang, Wu-Yang Zhang, and Jeff Z. Y. Chen</p><p> We study the disorder-order transition boundary of wormlile <span><span style="font-style: italic;">A</span><span style="font-style: italic;">B</span></span> diblock copolymers on the basis of the wormlike chain formalism aided by a self-consistent mean-field treatment. We examine the influence of the persistency on the phase diagram and properties of the phase transition as a function of the...</p><p>[Phys. Rev. E 84, 041803] Published Thu Oct 13, 2011</p>]]></content:encoded>
    <dc:title>Dependence of the disorder-lamellar stability boundary of a melt of asymmetric wormlike AB diblock copolymers on the chain rigidity</dc:title>
    <dc:creator>Ying Jiang, Wu-Yang Zhang, and Jeff Z. Y. Chen</dc:creator>
    <dc:date>2011-10-13T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041803</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041803 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-13T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041803</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041803</prism:url>
    <prism:startingPage>041803</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041802">
    <title>Polymer-induced entropic depletion potential</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041802</link>
    <description>Author(s): Xue-Zheng Cao, Holger Merlitz, Chen-Xu Wu, and Jens-Uwe Sommer&lt;br/&gt;&lt;p&gt;We study the effective interactions between nanoparticles immersed in an athermal polymer solution using Molecular dynamics. The directly measured polymer-induced depletion forces are well described with a scaling model in which the attraction between particles is caused by the depletion of concentr...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041802] Published Wed Oct 12, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Xue-Zheng Cao, Holger Merlitz, Chen-Xu Wu, and Jens-Uwe Sommer</p><p> We study the effective interactions between nanoparticles immersed in an athermal polymer solution using Molecular dynamics. The directly measured polymer-induced depletion forces are well described with a scaling model in which the attraction between particles is caused by the depletion of concentr...</p><p>[Phys. Rev. E 84, 041802] Published Wed Oct 12, 2011</p>]]></content:encoded>
    <dc:title>Polymer-induced entropic depletion potential</dc:title>
    <dc:creator>Xue-Zheng Cao, Holger Merlitz, Chen-Xu Wu, and Jens-Uwe Sommer</dc:creator>
    <dc:date>2011-10-12T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041802</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041802 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-12T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041802</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041802</prism:url>
    <prism:startingPage>041802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.041801">
    <title>Thermodynamic treatment of polymer thin-film glasses</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.041801</link>
    <description>Author(s): Ronald P. White and Jane E. G. Lipson&lt;br/&gt;&lt;p&gt;We propose a new, simple, thermodynamically based model in order to study the effect of film thickness on the glass transition of a polymer. The model equation of state incorporates the effect of a free surface by accounting for missing interactions, and is parametrized using experimental data for b...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 041801] Published Mon Oct 03, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Ronald P. White and Jane E. G. Lipson</p><p> We propose a new, simple, thermodynamically based model in order to study the effect of film thickness on the glass transition of a polymer. The model equation of state incorporates the effect of a free surface by accounting for missing interactions, and is parametrized using experimental data for b...</p><p>[Phys. Rev. E 84, 041801] Published Mon Oct 03, 2011</p>]]></content:encoded>
    <dc:title>Thermodynamic treatment of polymer thin-film glasses</dc:title>
    <dc:creator>Ronald P. White and Jane E. G. Lipson</dc:creator>
    <dc:date>2011-10-03T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.041801</dc:identifier>
    <dc:source>Phys. Rev. E 84, 041801 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>4</prism:number>
    <prism:publicationDate>2011-10-03T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.041801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.041801</prism:url>
    <prism:startingPage>041801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.031803">
    <title>Thermodynamics of polymer adsorption to a flexible membrane</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.031803</link>
    <description>Author(s): Steffen Karalus, Wolfhard Janke, and Michael Bachmann&lt;br/&gt;&lt;p&gt;We analyze the structural behavior of a single polymer chain grafted to an attractive, flexible surface. Our model is composed of a coarse-grained bead-and-spring polymer and a tethered membrane. By means of extensive parallel tempering Monte Carlo simulations it is shown that the system exhibits a ...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 031803] Published Wed Sep 21, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Steffen Karalus, Wolfhard Janke, and Michael Bachmann</p><p> We analyze the structural behavior of a single polymer chain grafted to an attractive, flexible surface. Our model is composed of a coarse-grained bead-and-spring polymer and a tethered membrane. By means of extensive parallel tempering Monte Carlo simulations it is shown that the system exhibits a ...</p><p>[Phys. Rev. E 84, 031803] Published Wed Sep 21, 2011</p>]]></content:encoded>
    <dc:title>Thermodynamics of polymer adsorption to a flexible membrane</dc:title>
    <dc:creator>Steffen Karalus, Wolfhard Janke, and Michael Bachmann</dc:creator>
    <dc:date>2011-09-21T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.031803</dc:identifier>
    <dc:source>Phys. Rev. E 84, 031803 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>3</prism:number>
    <prism:publicationDate>2011-09-21T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.031803</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.031803</prism:url>
    <prism:startingPage>031803</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.031802">
    <title>Interfacial properties of polystyrene thin films as revealed by neutron reflectivity</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.031802</link>
    <description>Author(s): Rintaro Inoue, Kazuko Kawashima, Kazuya Matsui, Makoto Nakamura, Koji Nishida, Toshiji Kanaya, and Norifumi L. Yamada&lt;br/&gt;&lt;p&gt;We have studied the glass transition temperature (&lt;span&gt;&lt;span style="font-style: italic;"&gt;T&lt;/span&gt;&lt;sub&gt;&lt;span style="font-style: italic;"&gt;g&lt;/span&gt;&lt;/sub&gt;&lt;/span&gt;) and molecular mobility of polystyrene (PS) thin films near the interface between the polymer thin film and substrate with bilayer thin films consisting of surface hydrogenated PS (h-PS) and bottom deuterated PS (d-PS) using neutron reflectivity. ...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 031802] Published Fri Sep 16, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Rintaro Inoue, Kazuko Kawashima, Kazuya Matsui, Makoto Nakamura, Koji Nishida, Toshiji Kanaya, and Norifumi L. Yamada</p><p> We have studied the glass transition temperature (<span><span style="font-style: italic;">T</span><sub><span style="font-style: italic;">g</span></sub></span>) and molecular mobility of polystyrene (PS) thin films near the interface between the polymer thin film and substrate with bilayer thin films consisting of surface hydrogenated PS (h-PS) and bottom deuterated PS (d-PS) using neutron reflectivity. ...</p><p>[Phys. Rev. E 84, 031802] Published Fri Sep 16, 2011</p>]]></content:encoded>
    <dc:title>Interfacial properties of polystyrene thin films as revealed by neutron reflectivity</dc:title>
    <dc:creator>Rintaro Inoue, Kazuko Kawashima, Kazuya Matsui, Makoto Nakamura, Koji Nishida, Toshiji Kanaya, and Norifumi L. Yamada</dc:creator>
    <dc:date>2011-09-16T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.031802</dc:identifier>
    <dc:source>Phys. Rev. E 84, 031802 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>3</prism:number>
    <prism:publicationDate>2011-09-16T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.031802</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.031802</prism:url>
    <prism:startingPage>031802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.031801">
    <title>First-principle approach to rescale the dynamics of simulated coarse-grained macromolecular liquids</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.031801</link>
    <description>Author(s): I. Lyubimov and M. G. Guenza&lt;br/&gt;&lt;p&gt;We present a detailed derivation and testing of our approach to rescale the dynamics of mesoscale simulations of coarse-grained polymer melts ( I. Y. Lyubimov, J. McCarty, A. Clark and M. G. Guenza &lt;a href="http://dx.doi.org/10.1063/1.3450301"&gt; J. Chem. Phys. &lt;span style="font-weight: bold;"&gt;132&lt;/span&gt; 224903 (2010)&lt;/a&gt;). Starting from the first-principle Liouville equation and applying ...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 031801] Published Tue Sep 13, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): I. Lyubimov and M. G. Guenza</p><p> We present a detailed derivation and testing of our approach to rescale the dynamics of mesoscale simulations of coarse-grained polymer melts ( I. Y. Lyubimov, J. McCarty, A. Clark and M. G. Guenza <a href="http://dx.doi.org/10.1063/1.3450301"> J. Chem. Phys. <span style="font-weight: bold;">132</span> 224903 (2010)</a>). Starting from the first-principle Liouville equation and applying ...</p><p>[Phys. Rev. E 84, 031801] Published Tue Sep 13, 2011</p>]]></content:encoded>
    <dc:title>First-principle approach to rescale the dynamics of simulated coarse-grained macromolecular liquids</dc:title>
    <dc:creator>I. Lyubimov and M. G. Guenza</dc:creator>
    <dc:date>2011-09-13T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.031801</dc:identifier>
    <dc:source>Phys. Rev. E 84, 031801 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>3</prism:number>
    <prism:publicationDate>2011-09-13T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.031801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.031801</prism:url>
    <prism:startingPage>031801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.021805">
    <title>Phase behavior and structure of stable complexes between a long polyanion and a branched polycation</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.021805</link>
    <description>Author(s): Valentina Mengarelli, Mehdi Zeghal, Loïc Auvray, and Daniel Clemens&lt;br/&gt;&lt;p&gt;The association between oppositely charged branched polyethylenimine (BPEI) and polymethacrylic acid (PMA) in the dilute regime is investigated using turbidimetric titration and electrophoretic mobility measurements. The complexation is controlled by tuning continuously the pH-sensitive charge of th...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 021805] Published Tue Aug 30, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Valentina Mengarelli, Mehdi Zeghal, Loïc Auvray, and Daniel Clemens</p><p> The association between oppositely charged branched polyethylenimine (BPEI) and polymethacrylic acid (PMA) in the dilute regime is investigated using turbidimetric titration and electrophoretic mobility measurements. The complexation is controlled by tuning continuously the pH-sensitive charge of th...</p><p>[Phys. Rev. E 84, 021805] Published Tue Aug 30, 2011</p>]]></content:encoded>
    <dc:title>Phase behavior and structure of stable complexes between a long polyanion and a branched polycation</dc:title>
    <dc:creator>Valentina Mengarelli, Mehdi Zeghal, Loïc Auvray, and Daniel Clemens</dc:creator>
    <dc:date>2011-08-30T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.021805</dc:identifier>
    <dc:source>Phys. Rev. E 84, 021805 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2011-08-30T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.021805</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.021805</prism:url>
    <prism:startingPage>021805</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.021804">
    <title>Conformation transitions of a polyelectrolyte chain: A replica-exchange Monte-Carlo study</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.021804</link>
    <description>Author(s): Peng Chi, Baohui Li, and An-Chang Shi&lt;br/&gt;&lt;p&gt;The thermodynamic behavior of a strongly charged polyelectrolyte chain immersed in a salt-free solution is studied using replica-exchange Monte-Carlo simulations. The results reveal that the chain can assume a variety of conformations, and it undergoes two phase transitions upon cooling. The first t...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 021804] Published Wed Aug 10, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Peng Chi, Baohui Li, and An-Chang Shi</p><p> The thermodynamic behavior of a strongly charged polyelectrolyte chain immersed in a salt-free solution is studied using replica-exchange Monte-Carlo simulations. The results reveal that the chain can assume a variety of conformations, and it undergoes two phase transitions upon cooling. The first t...</p><p>[Phys. Rev. E 84, 021804] Published Wed Aug 10, 2011</p>]]></content:encoded>
    <dc:title>Conformation transitions of a polyelectrolyte chain: A replica-exchange Monte-Carlo study</dc:title>
    <dc:creator>Peng Chi, Baohui Li, and An-Chang Shi</dc:creator>
    <dc:date>2011-08-10T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.021804</dc:identifier>
    <dc:source>Phys. Rev. E 84, 021804 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2011-08-10T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.021804</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.021804</prism:url>
    <prism:startingPage>021804</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.021803">
    <title>Shear-induced metastable states of end-grafted polystyrene</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.021803</link>
    <description>Author(s): Leslie A. Sasa, Eric J. Yearley, Michael S. Jablin, Robert D. Gilbertson, Adrienne S. Lavine, Jaroslaw Majewski, and Rex P. Hjelm&lt;br/&gt;&lt;p&gt;The &lt;span style="font-style: italic;"&gt;in situ&lt;/span&gt; molecular scale response of end-grafted polystyrene to shear against a deuterated polystyrene melt was investigated with neutron reflectometry. The derived grafted polystyrene density profiles showed that the grafted polystyrene was retained on the quartz wafer during the measurements. T...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 021803] Published Fri Aug 05, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Leslie A. Sasa, Eric J. Yearley, Michael S. Jablin, Robert D. Gilbertson, Adrienne S. Lavine, Jaroslaw Majewski, and Rex P. Hjelm</p><p> The <span style="font-style: italic;">in situ</span> molecular scale response of end-grafted polystyrene to shear against a deuterated polystyrene melt was investigated with neutron reflectometry. The derived grafted polystyrene density profiles showed that the grafted polystyrene was retained on the quartz wafer during the measurements. T...</p><p>[Phys. Rev. E 84, 021803] Published Fri Aug 05, 2011</p>]]></content:encoded>
    <dc:title>Shear-induced metastable states of end-grafted polystyrene</dc:title>
    <dc:creator>Leslie A. Sasa, Eric J. Yearley, Michael S. Jablin, Robert D. Gilbertson, Adrienne S. Lavine, Jaroslaw Majewski, and Rex P. Hjelm</dc:creator>
    <dc:date>2011-08-05T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.021803</dc:identifier>
    <dc:source>Phys. Rev. E 84, 021803 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2011-08-05T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.021803</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.021803</prism:url>
    <prism:startingPage>021803</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.022801">
    <title>Constrained random-force model for weakly bending semiflexible polymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.022801</link>
    <description>Author(s): Panayotis Benetatos and Eugene M. Terentjev&lt;br/&gt;&lt;p&gt;The random-force (Larkin) model of a directed elastic string subject to quenched random forces in the transverse directions has been a paradigm in the statistical physics of disordered systems. In this Brief Report, we investigate a modified version of the above model where the total transverse forc...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 022801] Published Thu Aug 04, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Panayotis Benetatos and Eugene M. Terentjev</p><p> The random-force (Larkin) model of a directed elastic string subject to quenched random forces in the transverse directions has been a paradigm in the statistical physics of disordered systems. In this Brief Report, we investigate a modified version of the above model where the total transverse forc...</p><p>[Phys. Rev. E 84, 022801] Published Thu Aug 04, 2011</p>]]></content:encoded>
    <dc:title>Constrained random-force model for weakly bending semiflexible polymers</dc:title>
    <dc:creator>Panayotis Benetatos and Eugene M. Terentjev</dc:creator>
    <dc:date>2011-08-04T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.022801</dc:identifier>
    <dc:source>Phys. Rev. E 84, 022801 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2011-08-04T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.022801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.022801</prism:url>
    <prism:startingPage>022801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.021802">
    <title>Stretching and migration of DNA by solvent elasticity in an oscillatory flow</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.021802</link>
    <description>Author(s): Wei-Chang Lo, H. C. Hong, H. J. Choi, Pik-Yin Lai, and C. K. Chan&lt;br/&gt;&lt;p&gt;A model with solution viscoelasticity is proposed to explain the ratchetlike stretching of DNA by a symmetric ac electric field in polymer solutions. In this model, DNA is stretched by the interaction between the fluid elasticity and the oscillatory flow induced by DNA. Predictions of the model are ...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 021802] Published Thu Aug 04, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Wei-Chang Lo, H. C. Hong, H. J. Choi, Pik-Yin Lai, and C. K. Chan</p><p> A model with solution viscoelasticity is proposed to explain the ratchetlike stretching of DNA by a symmetric ac electric field in polymer solutions. In this model, DNA is stretched by the interaction between the fluid elasticity and the oscillatory flow induced by DNA. Predictions of the model are ...</p><p>[Phys. Rev. E 84, 021802] Published Thu Aug 04, 2011</p>]]></content:encoded>
    <dc:title>Stretching and migration of DNA by solvent elasticity in an oscillatory flow</dc:title>
    <dc:creator>Wei-Chang Lo, H. C. Hong, H. J. Choi, Pik-Yin Lai, and C. K. Chan</dc:creator>
    <dc:date>2011-08-04T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.021802</dc:identifier>
    <dc:source>Phys. Rev. E 84, 021802 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2011-08-04T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.021802</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.021802</prism:url>
    <prism:startingPage>021802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.021801">
    <title>Biaxial deformations of rubber: A comparison between entanglement theory and elastic fluctuation theory</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.021801</link>
    <description>Author(s): Xiangjun Xing&lt;br/&gt;&lt;p&gt;The classical theory of rubber elasticity fails in the regime of large deformation. The underlying physical mechanism has been under debate for a long time. In this work, we test the recently proposed mechanism of thermal elastic fluctuations by Xing, Goldbart, and Radzihovsky (XGR) against the biax...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 021801] Published Wed Aug 03, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Xiangjun Xing</p><p> The classical theory of rubber elasticity fails in the regime of large deformation. The underlying physical mechanism has been under debate for a long time. In this work, we test the recently proposed mechanism of thermal elastic fluctuations by Xing, Goldbart, and Radzihovsky (XGR) against the biax...</p><p>[Phys. Rev. E 84, 021801] Published Wed Aug 03, 2011</p>]]></content:encoded>
    <dc:title>Biaxial deformations of rubber: A comparison between entanglement theory and elastic fluctuation theory</dc:title>
    <dc:creator>Xiangjun Xing</dc:creator>
    <dc:date>2011-08-03T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.021801</dc:identifier>
    <dc:source>Phys. Rev. E 84, 021801 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>2</prism:number>
    <prism:publicationDate>2011-08-03T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.021801</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.021801</prism:url>
    <prism:startingPage>021801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.011808">
    <title>Field-theoretical approach to a dense polymer with an ideal binary mixture of clustering centers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.011808</link>
    <description>Author(s): Riccardo Fantoni and Kristian K. Müller-Nedebock&lt;br/&gt;&lt;p&gt;We propose a field-theoretical approach to a polymer system immersed in an ideal mixture of clustering centers. The system contains several species of these clustering centers with different functionality, each of which connects a fixed number segments of the chain to each other. The field theory is...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 011808] Published Fri Jul 29, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): Riccardo Fantoni and Kristian K. Müller-Nedebock</p><p> We propose a field-theoretical approach to a polymer system immersed in an ideal mixture of clustering centers. The system contains several species of these clustering centers with different functionality, each of which connects a fixed number segments of the chain to each other. The field theory is...</p><p>[Phys. Rev. E 84, 011808] Published Fri Jul 29, 2011</p>]]></content:encoded>
    <dc:title>Field-theoretical approach to a dense polymer with an ideal binary mixture of clustering centers</dc:title>
    <dc:creator>Riccardo Fantoni and Kristian K. Müller-Nedebock</dc:creator>
    <dc:date>2011-07-29T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.011808</dc:identifier>
    <dc:source>Phys. Rev. E 84, 011808 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>1</prism:number>
    <prism:publicationDate>2011-07-29T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.011808</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.011808</prism:url>
    <prism:startingPage>011808</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.84.011807">
    <title>Polymer segmental cross correlations from dielectric relaxation spectra of block copolymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.84.011807</link>
    <description>Author(s): George D. J. Phillies&lt;br/&gt;&lt;p&gt;Dielectric relaxation spectra of solutions of block polymers containing sequential type-A dipoles are considered from a theoretical correlation-function standpoint. Spectra of a specific set of block copolymers can be combined to isolate the dynamic cross-correlation between the motions of two disti...&lt;/p&gt;&lt;br/&gt;[Phys. Rev. E 84, 011807] Published Mon Jul 25, 2011</description>
    <content:encoded><![CDATA[<p>Author(s): George D. J. Phillies</p><p> Dielectric relaxation spectra of solutions of block polymers containing sequential type-A dipoles are considered from a theoretical correlation-function standpoint. Spectra of a specific set of block copolymers can be combined to isolate the dynamic cross-correlation between the motions of two disti...</p><p>[Phys. Rev. E 84, 011807] Published Mon Jul 25, 2011</p>]]></content:encoded>
    <dc:title>Polymer segmental cross correlations from dielectric relaxation spectra of block copolymers</dc:title>
    <dc:creator>George D. J. Phillies</dc:creator>
    <dc:date>2011-07-25T10:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>doi:10.1103/PhysRevE.84.011807</dc:identifier>
    <dc:source>Phys. Rev. E 84, 011807 (2011)</dc:source>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>84</prism:volume>
    <prism:number>1</prism:number>
    <prism:publicationDate>2011-07-25T10:00:00-04:00</prism:publicationDate>
    <prism:doi>10.1103/PhysRevE.84.011807</prism:doi>
    <prism:url>http://link.aps.org/doi/10.1103/PhysRevE.84.011807</prism:url>
    <prism:startingPage>011807</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
</rdf:RDF>

