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  <title><![CDATA[PhD Defense by Tom Wyatt]]></title>
  <body><![CDATA[<p>PTFE PhD Defense - Tom Wyatt</p><p>&nbsp;</p><p>Date: April 30, 2015</p><p>Time: 1:05 PM</p><p>Location: MRDC 4404</p><p>&nbsp;</p><p>Committee:</p><p>Dr. Donggang Yao, MSE&nbsp;(Advisor)</p><p>Dr. Yulin Deng, ChBE</p><p>Dr. Anselm Griffin, MSE</p><p>Dr. Satish Kumar, MSE&nbsp;</p><p>Dr. Youjiang Wang, MSE</p><p>&nbsp;</p><p>Title:</p><p>Oligomer spin-solvent gel-fiber spinning</p><p>&nbsp;</p><p>Abstract:</p><p>&nbsp;</p><p>Successful processing of polymer molecules into well oriented fiber structures with minimal defects is difficult because the thermodynamically favorable state is a random coil, and molecular relaxation perpetually opposes efforts to extend and orient polymer molecules. This dissertation introduces the oligomer spin-solvent approach for gel-spinning high-strength fibers from many polymers with different chemistries. The theory is applied to two semi-crystalline, linear polymers without significant hydrogen bonding interactions: polyoxymethylene (POM) and polyethylene oxide (PEO). The resulting fibers are among the strongest POM and PEO fibers ever created. The efficiency of the gel-spinning process is increased through a mechanical solvent extraction method. By exploiting the unique solid-like behavior of the gel-fiber network, this work demonstrates that the spin-solvent can be separated from the gel-fiber by mechanically deforming the gel-network instead of chemically through an extraction solvent. A relatively safe and efficient gel-spinning process based on mechanical spin-solvent extraction is demonstrated using ultra-high molecular weight polyethylene.</p><p> </p>]]></body>
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