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        <identifier>oai:www.ideals.illinois.edu:2142/71853</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_47053</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Wool, Richard P.</dc:contributor>
          <dc:creator>Willett, Julious Lee</dc:creator>
          <dc:date>2014-12-16T20:52:18Z</dc:date>
          <dc:date>2014-12-16T20:52:18Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1988</dc:date>
          <dc:date>1988</dc:date>
          <dc:description>Mechanical strength of incompatible polymer interfaces welded above T$\sb{\rm g}$ has been investigated as a function of time, temperature, and composition. Three pairs of polymers were used: polystyrene-polymethylmethacrylate, polystyrene-co-acrylonitrile-polymethylmethacrylate, and polystyrene-co-acrylonitrile-polycarbonate. For each pair, the weld strength, as measured by G$\sb{\rm IC}$, attained a constant value which increased with welding temperature. While only five to ten percent of bulk G$\sb{\rm IC}$ values, these plateau values are orders of magnitude greater than the work of adhesion calculated using intermolecular forces. For the copolymer-homopolymer pairs, the maximum plateau strength was reached when the interaction parameter was a minimum. These results are in agreement with a model of the interface based on current molecular theories of incompatible interfaces coupled with a chain pull out microstructural deformation mechanism, which predicts that G$\sb{\rm IC}$ increases inversely with the interaction parameter, X. Microscopic investigation of the fracture surfaces revealed dissimilar fracture surfaces for a given pair, with evidence of stick-slip crack growth. X-ray photoelectron spectroscopy revealed residues of one polymer on the other's surface, indicating cohesive fracture occurred to some extent; in each case, the residue was always from the polymer with the lower entanglement density.</dc:description>
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8823290.pdf: 5113962 bytes, checksum: 87c04810974abd02dc1478a14f973517 (MD5)
  Previous issue date: 1988</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 72019
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>221 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1988.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/71853</dc:identifier>
          <dc:identifier>(UMI)AAI8823290</dc:identifier>
          <dc:subject>Engineering, Materials Science</dc:subject>
          <dc:title>Strength Development at Incompatible Polymer Interfaces</dc:title>
          <dc:type>text</dc:type>
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            <department>Metallurgy and Mining Engineering</department>
            <discipline>Metallurgical Engineering</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
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