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    <description>Recently published articles in Phys. Rev. E in the Table of Content section "Polymers"</description>
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    <dc:rights>Copyright (c) 2009 The American Physical Society</dc:rights>
    <dc:date>2009-11-22T06:18:14-05:00</dc:date>
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    <title>Bending affects entropy of semiflexible polymers: Application to protein-DNA complexes</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.052801</link>
    <description>Author(s): Shay M. Rappaport and Yitzhak Rabin&lt;br/&gt;We discuss a class of generalized wormlike chain models of polymers with spontaneous curvature and show that the density of states and consequently the entropy of such natively bent polymers are higher than that of straight ones. This effect changes the classical Langmuir binding isotherm by giving ...&lt;br/&gt;[Phys. Rev. E 80, 052801] Published Thu Nov 12, 2009</description>
    <dc:creator>Shay M. Rappaport and Yitzhak Rabin</dc:creator>
    <dc:date>2009-11-12T00:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.052801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 052801</dc:source>
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    <title>Ordering of a lamella-forming fluid near an interface</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.051803</link>
    <description>Author(s): Andrew B. Croll, An-Chang Shi, and Kari Dalnoki-Veress&lt;br/&gt;By using wedged thin films, we have measured the effect of interfaces on the ordering of an anisotropic fluid in real space. Symmetric diblock copolymers can form an ordered lamellar fluid, and the preference of the substrate for one of the blocks can induce order well into the disordered bulk phase...&lt;br/&gt;[Phys. Rev. E 80, 051803] Published Wed Nov 11, 2009</description>
    <dc:creator>Andrew B. Croll, An-Chang Shi, and Kari Dalnoki-Veress</dc:creator>
    <dc:date>2009-11-11T00:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.051803</dc:identifier>
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    <title>Aging dynamics in the polymer glass of poly(2-chlorostyrene): Dielectric susceptibility and volume</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.051802</link>
    <description>Author(s): Koji Fukao and Daisuke Tahara&lt;br/&gt;Aging dynamics was investigated in the glassy states of poly(2-chlorostyrene) by measuring the complex electrical capacitance during aging below the glass transition temperature. The variations with time and temperature of the ac dielectric susceptibility and volume could be determined by simply mea...&lt;br/&gt;[Phys. Rev. E 80, 051802] Published Tue Nov 10, 2009</description>
    <dc:creator>Koji Fukao and Daisuke Tahara</dc:creator>
    <dc:date>2009-11-10T00:00:00-05:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.051802</dc:identifier>
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    <title>Experimental observation of effects of seeds on polymer crystallization</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.051801</link>
    <description>Author(s): Peng-Wei Zhu, Andy Phillips, Graham Edward, and Lance Nichols&lt;br/&gt;The effects of two seeds on the melt crystallization of isotactic polypropylene were experimentally investigated. The seed, which has the flat surface full of a nonuniform size distribution, has provided a right surface pattern to activate effectively the heterogeneous nucleation. In contrast, the s...&lt;br/&gt;[Phys. Rev. E 80, 051801] Published Tue Nov 03, 2009</description>
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    <dc:date>2009-11-03T00:00:00-05:00</dc:date>
    <dc:rights>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.80.041809" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Renormalized field theory of collapsing directed randomly branched polymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041809</link>
    <description>Author(s): Hans-Karl Janssen, Frank Wevelsiep, and Olaf Stenull&lt;br/&gt;We present a dynamical field theory for directed randomly branched polymers and in particular their collapse transition. We develop a phenomenological model in the form of a stochastic response functional that allows us to address several interesting problems such as the scaling behavior of the swol...&lt;br/&gt;[Phys. Rev. E 80, 041809] Published Fri Oct 30, 2009</description>
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    <dc:date>2009-10-30T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041809</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041809</dc:source>
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  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.041808" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Entangled chain dynamics of polymer knots in extensional flow</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041808</link>
    <description>Author(s): Demosthenes Kivotides, S. Louise Wilkin, and Theo G. Theofanous&lt;br/&gt;We formulate a coarse-grained molecular-dynamics model of polymer chains in solution that includes hydrodynamic interactions, thermal fluctuations, nonlinear elasticity, and topology-preserving solvent mediated excluded volume interactions. The latter involve a combination of potential forces with e...&lt;br/&gt;[Phys. Rev. E 80, 041808] Published Thu Oct 29, 2009</description>
    <dc:creator>Demosthenes Kivotides, S. Louise Wilkin, and Theo G. Theofanous</dc:creator>
    <dc:date>2009-10-29T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041808</dc:identifier>
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    <title>Microscopic density functional theory for dendrimers</title>
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    <description>Author(s): Alexandr Malijevsk&#253;&lt;br/&gt;Density functional theory for a simple model of dendrimers is proposed. The theory is based on fundamental measure theory, which accounts for the hard-sphere repulsion of the segments and on the Wertheim first-order perturbation theory for the correlations due to connectivity. Set of the recurrence ...&lt;br/&gt;[Phys. Rev. E 80, 042801] Published Tue Oct 27, 2009</description>
    <dc:creator>Alexandr Malijevsk&#253;</dc:creator>
    <dc:date>2009-10-27T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.042801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 042801</dc:source>
    <dc:format>text/html</dc:format>
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    <prism:publicationDate>2009-10-27T00:00:00-04:00</prism:publicationDate>
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    <dc:subject>Polymers</dc:subject>
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  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.041807" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Storage shear modulus of columnar structure formed in an immiscible polymer blend under electric fields</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041807</link>
    <description>Author(s): Kohei Aida, Yang Ho Na, Tomoyuki Nagaya, and Hiroshi Orihara&lt;br/&gt;Oscillatory measurements of a columnar structure were performed, which was formed in an immiscible polymer blend subjected to an electric field. The formation process was observed through a confocal scanning laser microscope and the structure for the measurements was confirmed to be well defined. Th...&lt;br/&gt;[Phys. Rev. E 80, 041807] Published Mon Oct 26, 2009</description>
    <dc:creator>Kohei Aida, Yang Ho Na, Tomoyuki Nagaya, and Hiroshi Orihara</dc:creator>
    <dc:date>2009-10-26T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041807</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041807</dc:source>
    <dc:format>text/html</dc:format>
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    <dc:subject>Polymers</dc:subject>
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  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.041806" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Conformational free energy of melts of ring-linear polymer blends</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041806</link>
    <description>Author(s): Gopinath Subramanian and Sachin Shanbhag&lt;br/&gt;The conformational free energy of ring polymers in a blend of ring and linear polymers is investigated using the bond-fluctuation model. Previously established scaling relationships for the free energy of a ring polymer are shown to be valid only in the mean-field sense, and alternative functional f...&lt;br/&gt;[Phys. Rev. E 80, 041806] Published Wed Oct 21, 2009</description>
    <dc:creator>Gopinath Subramanian and Sachin Shanbhag</dc:creator>
    <dc:date>2009-10-21T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041806</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041806</dc:source>
    <dc:format>text/html</dc:format>
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    <prism:publicationName>Physical Review E</prism:publicationName>
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    <prism:publicationDate>2009-10-21T00:00:00-04:00</prism:publicationDate>
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    <dc:subject>Polymers</dc:subject>
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  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.041805" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Characterization of the &#8220;simple-liquid&#8221; state in a polymeric system: Coherent and incoherent scattering functions</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041805</link>
    <description>Author(s): A. Arbe and J. Colmenero&lt;br/&gt;By means of time-of-flight neutron scattering, we have characterized the dynamic structure factor and the hydrogen motions of polyethylene above its melting point. As signatures of simple-liquid dynamics, we observe that (i) in the explored dynamic window, the intermediate scattering functions displ...&lt;br/&gt;[Phys. Rev. E 80, 041805] Published Wed Oct 14, 2009</description>
    <dc:creator>A. Arbe and J. Colmenero</dc:creator>
    <dc:date>2009-10-14T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041805</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041805</dc:source>
    <dc:format>text/html</dc:format>
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    <prism:publicationName>Physical Review E</prism:publicationName>
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    <prism:publicationDate>2009-10-14T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>041805</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
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  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.041804" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Grand-canonical and canonical solution of self-avoiding walks with up to three monomers per site on the Bethe lattice</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041804</link>
    <description>Author(s): Tiago J. Oliveira, J&#252;rgen F. Stilck, and Pablo Serra&lt;br/&gt;We solve a model of polymers represented by self-avoiding walks on a lattice, which may visit the same site up to three times in the grand-canonical formalism on the Bethe lattice. This may be a model for the collapse transition of polymers where only interactions between monomers at the same site a...&lt;br/&gt;[Phys. Rev. E 80, 041804] Published Wed Oct 14, 2009</description>
    <dc:creator>Tiago J. Oliveira, J&#252;rgen F. Stilck, and Pablo Serra</dc:creator>
    <dc:date>2009-10-14T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041804</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041804</dc:source>
    <dc:format>text/html</dc:format>
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    <dc:subject>Polymers</dc:subject>
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    <title>Detailed scaling analysis of low-force polyelectrolyte elasticity</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041803</link>
    <description>Author(s): D. B. McIntosh, N. Ribeck, and O. A. Saleh&lt;br/&gt;Single-molecule force-extension data are typically compared to ideal models of polymer behavior that ignore the effects of self-avoidance. Here, we demonstrate a link between single-molecule data and the scaling pictures of a real polymer. We measure a low-force elasticity regime where the extension...&lt;br/&gt;[Phys. Rev. E 80, 041803] Published Wed Oct 07, 2009</description>
    <dc:creator>D. B. McIntosh, N. Ribeck, and O. A. Saleh</dc:creator>
    <dc:date>2009-10-07T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041803</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041803</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>4</prism:issueIdentifier>
    <prism:publicationDate>2009-10-07T00:00:00-04:00</prism:publicationDate>
    <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.80.041802" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Polymer chains in confined geometries: Massive field theory approach</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041802</link>
    <description>Author(s): D. Romeis and Z. Usatenko&lt;br/&gt;The massive field theory approach in fixed space dimensions d&lt;4 is applied to investigate a dilute solution of long-flexible polymer chains in a good solvent between two parallel repulsive walls, two inert walls, and for the mixed case of one inert and one repulsive wall. The well-known correspondence between the field theoretical &#981;^{4} O(n) -vector model in the limit n&#8594;0 and the behavior of long-flexible polymer chains in a good solvent is used to calculate the depletion interaction potential and the depletion force up to one-loop order. In order to make the theory UV finite in renormalization-group sense in 3&#8804;d&lt;4 dimensions we performed the standard mass renormalization and additional surface-enhancement constants renormalization. Besides, our investigations include modification of renormalization scheme for the case of two inert walls. The obtained results confirm that the depletion interaction potential and the resulting depletion force between two repulsive walls are weaker for chains with excluded volume interaction (EVI) than for ideal chains because the EVI effectively reduces the depletion effect near the walls. Our results are in qualitative agreement with previous theoretical investigations, experimental results, and with the results of Monte Carlo simulations.&lt;br/&gt;[Phys. Rev. E 80, 041802] Published Wed Oct 07, 2009</description>
    <dc:creator>D. Romeis and Z. Usatenko</dc:creator>
    <dc:date>2009-10-07T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041802</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041802</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>4</prism:issueIdentifier>
    <prism:publicationDate>2009-10-07T00:00:00-04:00</prism:publicationDate>
    <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.80.041801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Microphase separation of comb copolymers with two different lengths of side chains</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.041801</link>
    <description>Author(s): M. A. Aliev and N. Yu. Kuzminyh&lt;br/&gt;The phase behavior of the monodisperse AB comb copolymer melt contained the macromolecules of special architecture is discussed. Each macromolecule is assumed to be composed of two comb blocks which differ in numbers of side chains and numbers of monomer units in these chains. It is shown (by analys...&lt;br/&gt;[Phys. Rev. E 80, 041801] Published Tue Oct 06, 2009</description>
    <dc:creator>M. A. Aliev and N. Yu. Kuzminyh</dc:creator>
    <dc:date>2009-10-06T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.041801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 041801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>4</prism:issueIdentifier>
    <prism:publicationDate>2009-10-06T00:00:00-04:00</prism:publicationDate>
    <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.80.040801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Tension dynamics and viscoelasticity of extensible wormlike chains</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.040801</link>
    <description>Author(s): Benedikt Obermayer and Erwin Frey&lt;br/&gt;The dynamic response of prestressed semiflexible biopolymers is characterized by the propagation and relaxation of tension, which arises due to the near inextensibility of a stiff backbone. It is coupled to the dynamics of contour length stored in thermal undulations but also to the local relaxation...&lt;br/&gt;&lt;img src="http://prola.aps.org/graphics/rapid30x30.gif" width="30" height="30" alt="Rapid Communication"/&gt;&lt;br/&gt;[Phys. Rev. E 80, 040801] Published Fri Oct 02, 2009</description>
    <dc:creator>Benedikt Obermayer and Erwin Frey</dc:creator>
    <dc:date>2009-10-02T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.040801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 040801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>4</prism:issueIdentifier>
    <prism:publicationDate>2009-10-02T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>040801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.031803" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Topological analysis of polymeric melts: Chain-length effects and fast-converging estimators for entanglement length</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.031803</link>
    <description>Author(s): Robert S. Hoy, Katerina Foteinopoulou, and Martin Kr&#246;ger&lt;br/&gt;Primitive path analyses of entanglements are performed over a wide range of chain lengths for both bead spring and atomistic polyethylene polymer melts. Estimators for the entanglement length N_{e} which operate on results for a single chain length N are shown to produce systematic O(1/N) errors. Th...&lt;br/&gt;[Phys. Rev. E 80, 031803] Published Tue Sep 29, 2009</description>
    <dc:creator>Robert S. Hoy, Katerina Foteinopoulou, and Martin Kr&#246;ger</dc:creator>
    <dc:date>2009-09-29T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.031803</dc:identifier>
    <dc:source>Phys. Rev. E 80, 031803</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>3</prism:issueIdentifier>
    <prism:publicationDate>2009-09-29T00:00:00-04:00</prism:publicationDate>
    <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.80.031802" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Glass transition and molecular mobility in polymer thin films</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.031802</link>
    <description>Author(s): R. Inoue, T. Kanaya, K. Nishida, I. Tsukushi, M. T. F. Telling, B. J. Gabrys, M. Tyagi, C. Soles, and W.-l. Wu&lt;br/&gt;Extensive studies on polymer thin films to date have revealed their interesting but unusual properties such as film thickness dependence of glass transition temperature T_{g} and thermal expansivity. Recent studies have shown that the lower T_{g} is not always related to the higher mobility in polym...&lt;br/&gt;[Phys. Rev. E 80, 031802] Published Tue Sep 22, 2009</description>
    <dc:creator>R. Inoue, T. Kanaya, K. Nishida, I. Tsukushi, M. T. F. Telling, B. J. Gabrys, M. Tyagi, C. Soles, and W.-l. Wu</dc:creator>
    <dc:date>2009-09-22T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.031802</dc:identifier>
    <dc:source>Phys. Rev. E 80, 031802</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>3</prism:issueIdentifier>
    <prism:publicationDate>2009-09-22T00:00:00-04:00</prism:publicationDate>
    <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.80.031801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Gel-like elasticity in glass-forming side-chain liquid-crystal polymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.031801</link>
    <description>Author(s): O. Pozo, D. Collin, H. Finkelmann, D. Rogez, and P. Martinoty&lt;br/&gt;We study the complex shear modulus G of two side-chain liquid-crystal polymers (SCLCPs), a methoxy-phenylbenzoate substituted polyacrylate (thereafter called PAOCH_{3} ), and a cyanobiphenyl substituted polyacrylate supplied by Merck (thereafter called LCP105) using a piezoelectric rheometer. Two me...&lt;br/&gt;[Phys. Rev. E 80, 031801] Published Tue Sep 22, 2009</description>
    <dc:creator>O. Pozo, D. Collin, H. Finkelmann, D. Rogez, and P. Martinoty</dc:creator>
    <dc:date>2009-09-22T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.031801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 031801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>3</prism:issueIdentifier>
    <prism:publicationDate>2009-09-22T00:00:00-04:00</prism:publicationDate>
    <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.80.030801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Deformation mechanism of nanocomposite gels studied by contrast variation small-angle neutron scattering</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.030801</link>
    <description>Author(s): Toshihiko Nishida, Hitoshi Endo, Noboru Osaka, Huan-jun Li, Kazutoshi Haraguchi, and Mitsuhiro Shibayama&lt;br/&gt;Contrast-variation small-angle neutron scattering (CV-SANS) was applied to investigate the deformation mechanism of high-performance nanocomposite polymer hydrogels (NC gels) consisting of polymer chains and inorganic clay platelets. Anisotropic SANS functions were obtained at various stretching rat...&lt;br/&gt;&lt;img src="http://prola.aps.org/graphics/rapid30x30.gif" width="30" height="30" alt="Rapid Communication"/&gt;&lt;br/&gt;[Phys. Rev. E 80, 030801] Published Mon Sep 14, 2009</description>
    <dc:creator>Toshihiko Nishida, Hitoshi Endo, Noboru Osaka, Huan-jun Li, Kazutoshi Haraguchi, and Mitsuhiro Shibayama</dc:creator>
    <dc:date>2009-09-14T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.030801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 030801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>3</prism:issueIdentifier>
    <prism:publicationDate>2009-09-14T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>030801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.021801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Structure and stability of helices in square-well homopolymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.021801</link>
    <description>Author(s): M. N. Bannerman, J. E. Magee, and L. Lue&lt;br/&gt;Recently, it has been demonstrated [Magee , Phys. Rev. Lett. 96, 207802 (2006)] that isolated square-well homopolymers can spontaneously break chiral symmetry and &#8220;freeze&#8221; into helical structures at sufficiently low temperatures. This behavior is interesting because the square-well homopolymer i...&lt;br/&gt;[Phys. Rev. E 80, 021801] Published Wed Aug 26, 2009</description>
    <dc:creator>M. N. Bannerman, J. E. Magee, and L. Lue</dc:creator>
    <dc:date>2009-08-26T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.021801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 021801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>2</prism:issueIdentifier>
    <prism:publicationDate>2009-08-26T00:00:00-04:00</prism:publicationDate>
    <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.80.020801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Predicted electric-field-induced hexatic structure in an ionomer membrane</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.020801</link>
    <description>Author(s): Elshad Allahyarov and Philip L. Taylor&lt;br/&gt;Coarse-grained molecular-dynamics simulations were used to study the morphological changes induced in a Nafion&#174;-like ionomer by the imposition of a strong electric field. We observe the formation of structures aligned along the direction of the applied field. The polar head groups of the ionomer si...&lt;br/&gt;&lt;img src="http://prola.aps.org/graphics/rapid30x30.gif" width="30" height="30" alt="Rapid Communication"/&gt;&lt;br/&gt;[Phys. Rev. E 80, 020801] Published Mon Aug 24, 2009</description>
    <dc:creator>Elshad Allahyarov and Philip L. Taylor</dc:creator>
    <dc:date>2009-08-24T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.020801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 020801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>2</prism:issueIdentifier>
    <prism:publicationDate>2009-08-24T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>020801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.010801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Interactions between planar stiff polyelectrolyte brushes</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.010801</link>
    <description>Author(s): Aaron Wynveen and Christos N. Likos&lt;br/&gt;Molecular-dynamics simulations were performed for two opposing flat surfaces sparsely grafted with rigid polyelectrolyte chains whose lengths are smaller than their persistence lengths. The resulting force-distance dependence was analyzed theoretically in terms of two separate physical mechanisms: t...&lt;br/&gt;&lt;img src="http://prola.aps.org/graphics/rapid30x30.gif" width="30" height="30" alt="Rapid Communication"/&gt;&lt;br/&gt;[Phys. Rev. E 80, 010801] Published Fri Jul 31, 2009</description>
    <dc:creator>Aaron Wynveen and Christos N. Likos</dc:creator>
    <dc:date>2009-07-31T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.010801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 010801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>1</prism:issueIdentifier>
    <prism:publicationDate>2009-07-31T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>010801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.011803" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Induced orientational effects in relaxation of polymer melts</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.011803</link>
    <description>Author(s): J. M. Deutsch and J. H. Pixley&lt;br/&gt;We study stress relaxation in bidisperse entangled polymer solutions. Shorter chains embedded in a majority of longer ones are known to be oriented by coupling to them. We analyze the mechanism for this both by computer simulation and theoretically. We show that the results can be understood in term...&lt;br/&gt;[Phys. Rev. E 80, 011803] Published Fri Jul 24, 2009</description>
    <dc:creator>J. M. Deutsch and J. H. Pixley</dc:creator>
    <dc:date>2009-07-24T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.011803</dc:identifier>
    <dc:source>Phys. Rev. E 80, 011803</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>1</prism:issueIdentifier>
    <prism:publicationDate>2009-07-24T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>011803</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.011802" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Thermodynamics of tubelike flexible polymers</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.011802</link>
    <description>Author(s): Thomas Vogel, Thomas Neuhaus, Michael Bachmann, and Wolfhard Janke&lt;br/&gt;In this work, we discuss the general phase behavior of short tubelike flexible polymers. The geometric thickness constraint is implemented through the concept of the global radius of curvature. We use sophisticated Monte Carlo sampling methods to simulate small bead-stick polymer models with Lennard...&lt;br/&gt;[Phys. Rev. E 80, 011802] Published Thu Jul 16, 2009</description>
    <dc:creator>Thomas Vogel, Thomas Neuhaus, Michael Bachmann, and Wolfhard Janke</dc:creator>
    <dc:date>2009-07-16T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.011802</dc:identifier>
    <dc:source>Phys. Rev. E 80, 011802</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>1</prism:issueIdentifier>
    <prism:publicationDate>2009-07-16T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>011802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.80.011801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Statistical mechanical modeling of catalytic polymerization within surface-functionalized mesoporous materials</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.80.011801</link>
    <description>Author(s): Da-Jiang Liu, Hung-Ting Chen, Victor S.-Y. Lin, and J. W. Evans&lt;br/&gt;A discrete lattice model is developed to describe diffusion-mediated polymerization occurring within mesopores, where reaction is enhanced at catalytic sites distributed within the interior of the pores. Diffusive transport of monomers and polymers is one-dimensional, diffusion coefficients for the ...&lt;br/&gt;[Phys. Rev. E 80, 011801] Published Mon Jul 06, 2009</description>
    <dc:creator>Da-Jiang Liu, Hung-Ting Chen, Victor S.-Y. Lin, and J. W. Evans</dc:creator>
    <dc:date>2009-07-06T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.80.011801</dc:identifier>
    <dc:source>Phys. Rev. E 80, 011801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>80</prism:volume>
    <prism:issueIdentifier>1</prism:issueIdentifier>
    <prism:publicationDate>2009-07-06T00:00:00-04:00</prism:publicationDate>
    <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.79.060801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Microphase separation in nanocomposite gels</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.79.060801</link>
    <description>Author(s): Noboru Osaka, Hitoshi Endo, Toshihiko Nishida, Takuya Suzuki, Huan-jun Li, Kazutoshi Haraguchi, and Mitsuhiro Shibayama&lt;br/&gt;Microphase separation in poly( N -isopropylacrylamide)(PNIPA)-clay nanocomposite hydrogels (NC gels) is investigated by means of contrast-variation small-angle neutron scattering (CV-SANS) and dynamic light scattering (DLS). By using CV-SANS, it is revealed that microphase separation occurs in NC ge...&lt;br/&gt;&lt;img src="http://prola.aps.org/graphics/rapid30x30.gif" width="30" height="30" alt="Rapid Communication"/&gt;&lt;br/&gt;[Phys. Rev. E 79, 060801] Published Mon Jun 15, 2009</description>
    <dc:creator>Noboru Osaka, Hitoshi Endo, Toshihiko Nishida, Takuya Suzuki, Huan-jun Li, Kazutoshi Haraguchi, and Mitsuhiro Shibayama</dc:creator>
    <dc:date>2009-06-15T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.79.060801</dc:identifier>
    <dc:source>Phys. Rev. E 79, 060801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>79</prism:volume>
    <prism:issueIdentifier>6</prism:issueIdentifier>
    <prism:publicationDate>2009-06-15T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>060801</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.79.061802" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Mechanical behavior of highly cross-linked polymer networks and its links to microscopic structure</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.79.061802</link>
    <description>Author(s): Debashish Mukherji and Cameron F. Abrams&lt;br/&gt;Highly cross-linked polymer (HCP) networks are becoming increasingly important as high-performance adhesives and multifunctional composite materials. Because of their cross-linked molecular architectures, HCPs can be strong but brittle. One key goal in improving the performance of an HCP is to incre...&lt;br/&gt;[Phys. Rev. E 79, 061802] Published Mon Jun 08, 2009</description>
    <dc:creator>Debashish Mukherji and Cameron F. Abrams</dc:creator>
    <dc:date>2009-06-08T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.79.061802</dc:identifier>
    <dc:source>Phys. Rev. E 79, 061802</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>79</prism:volume>
    <prism:issueIdentifier>6</prism:issueIdentifier>
    <prism:publicationDate>2009-06-08T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>061802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
  <item rdf:about="http://link.aps.org/doi/10.1103/PhysRevE.79.061801" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Water harvesting using a conducting polymer: A study by molecular dynamics simulation</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.79.061801</link>
    <description>Author(s): Mayur M. Ostwal, Muhammad Sahimi, and Theodore T. Tsotsis&lt;br/&gt;The results of extensive molecular simulations of adsorption and diffusion of water vapor in polyaniline, made conducting by doping it with HCl or HBr over a broad range of temperatures, are reported. The atomistic model of the polymers was generated using energy minimization, equilibrium molecular ...&lt;br/&gt;[Phys. Rev. E 79, 061801] Published Wed Jun 03, 2009</description>
    <dc:creator>Mayur M. Ostwal, Muhammad Sahimi, and Theodore T. Tsotsis</dc:creator>
    <dc:date>2009-06-03T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.79.061801</dc:identifier>
    <dc:source>Phys. Rev. E 79, 061801</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>79</prism:volume>
    <prism:issueIdentifier>6</prism:issueIdentifier>
    <prism:publicationDate>2009-06-03T00:00:00-04:00</prism:publicationDate>
    <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.79.051802" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Influence of the torsional potential on the glass transition temperature and the structure of amorphous polyethylene</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.79.051802</link>
    <description>Author(s): Manel Canales&lt;br/&gt;The effect of the torsional potential on several thermodynamic and structural properties of a system of polyethylene chains has been analyzed. To this end, molecular dynamics simulations of a coarse-grained model, whose sites interact through a force field with bending, torsional, and nonbonded term...&lt;br/&gt;[Phys. Rev. E 79, 051802] Published Thu May 28, 2009</description>
    <dc:creator>Manel Canales</dc:creator>
    <dc:date>2009-05-28T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.79.051802</dc:identifier>
    <dc:source>Phys. Rev. E 79, 051802</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>79</prism:volume>
    <prism:issueIdentifier>5</prism:issueIdentifier>
    <prism:publicationDate>2009-05-28T00:00:00-04:00</prism:publicationDate>
    <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.79.050802" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/">
    <title>Perimeter length and form factor in two-dimensional polymer melts</title>
    <link>http://link.aps.org/doi/10.1103/PhysRevE.79.050802</link>
    <description>Author(s): H. Meyer, T. Kreer, M. Aichele, A. Cavallo, A. Johner, J. Baschnagel, and J. P. Wittmer&lt;br/&gt;Self-avoiding polymers in two-dimensional (d=2) melts are known to adopt compact configurations of typical size R(N)&#8764;N^{1/d} , with N being the chain length. Using molecular-dynamics simulations we show that the irregular shapes of these chains are characterized by a perimeter length L(N)&#8764;R(N)^{...&lt;br/&gt;&lt;img src="http://prola.aps.org/graphics/rapid30x30.gif" width="30" height="30" alt="Rapid Communication"/&gt;&lt;br/&gt;[Phys. Rev. E 79, 050802] Published Thu May 21, 2009</description>
    <dc:creator>H. Meyer, T. Kreer, M. Aichele, A. Cavallo, A. Johner, J. Baschnagel, and J. P. Wittmer</dc:creator>
    <dc:date>2009-05-21T00:00:00-04:00</dc:date>
    <dc:rights>Personal use only, all commercial or other reuse prohibited</dc:rights>
    <dc:identifier>10.1103/PhysRevE.79.050802</dc:identifier>
    <dc:source>Phys. Rev. E 79, 050802</dc:source>
    <dc:format>text/html</dc:format>
    <dc:type>article</dc:type>
    <prism:publicationName>Physical Review E</prism:publicationName>
    <prism:volume>79</prism:volume>
    <prism:issueIdentifier>5</prism:issueIdentifier>
    <prism:publicationDate>2009-05-21T00:00:00-04:00</prism:publicationDate>
    <prism:startingPage>050802</prism:startingPage>
    <dc:subject>Polymers</dc:subject>
    <prism:section>Polymers</prism:section>
  </item>
</rdf:RDF>
