Plastic Deformation of Semicrystalline Polyethylene by X‑ray Scattering: Comparison with Atomistic Simulations
Plastic deformation of uniaxially oriented polyethylene (PE) fiber has been examined by small and wide angle synchrotron X-ray scattering. Morphology changes of the lamellar stack with deformation beyond yielding have been characterized and quantified. Atomistic simulations of tensile deformation of...
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Veröffentlicht in: | Macromolecules 2013-07, Vol.46 (13), p.5279-5289 |
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creator | Che, Justin Locker, C. Rebecca Lee, Sanghun Rutledge, Gregory C Hsiao, Benjamin S Tsou, Andy H |
description | Plastic deformation of uniaxially oriented polyethylene (PE) fiber has been examined by small and wide angle synchrotron X-ray scattering. Morphology changes of the lamellar stack with deformation beyond yielding have been characterized and quantified. Atomistic simulations of tensile deformation of the lamellar stack in the longitudinal direction compare favorably to the experimentally observed morphological changes in the PE fiber. Experimental deformations at 100 °C exhibit responses comparable to those observed by simulation of deformation with constant total volume at 77 °C and a strain rate of 5 × 106 s–1. Experimental deformations of the PE fiber at 25 °C were found to be comparable to simulated tensile deformation with constant lateral dimensions at 77 °C and a strain rate of 5 × 107 s–1. Cavitation in the interlamellar region was found experimentally in the PE fiber deforming at room temperature as predicted by simulation with constant lateral dimensions at the higher strain rate. Melting, recrystallization, and removal of entanglements observed in the PE fiber deformation at 100 °C agree with the simulation results of a constant volume deformation at the slower strain rate. The ability to define the deformation behavior of PE at room and at high temperatures through simulation offers unique opportunities to examine how the interlamellar amorphous topology affects PE deformation. |
doi_str_mv | 10.1021/ma4005007 |
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Rebecca ; Lee, Sanghun ; Rutledge, Gregory C ; Hsiao, Benjamin S ; Tsou, Andy H</creator><creatorcontrib>Che, Justin ; Locker, C. Rebecca ; Lee, Sanghun ; Rutledge, Gregory C ; Hsiao, Benjamin S ; Tsou, Andy H ; Brookhaven National Laboratory (BNL)</creatorcontrib><description>Plastic deformation of uniaxially oriented polyethylene (PE) fiber has been examined by small and wide angle synchrotron X-ray scattering. Morphology changes of the lamellar stack with deformation beyond yielding have been characterized and quantified. Atomistic simulations of tensile deformation of the lamellar stack in the longitudinal direction compare favorably to the experimentally observed morphological changes in the PE fiber. Experimental deformations at 100 °C exhibit responses comparable to those observed by simulation of deformation with constant total volume at 77 °C and a strain rate of 5 × 106 s–1. Experimental deformations of the PE fiber at 25 °C were found to be comparable to simulated tensile deformation with constant lateral dimensions at 77 °C and a strain rate of 5 × 107 s–1. Cavitation in the interlamellar region was found experimentally in the PE fiber deforming at room temperature as predicted by simulation with constant lateral dimensions at the higher strain rate. Melting, recrystallization, and removal of entanglements observed in the PE fiber deformation at 100 °C agree with the simulation results of a constant volume deformation at the slower strain rate. The ability to define the deformation behavior of PE at room and at high temperatures through simulation offers unique opportunities to examine how the interlamellar amorphous topology affects PE deformation.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma4005007</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Fibers and threads ; Forms of application and semi-finished materials ; Polymer industry, paints, wood ; Technology of polymers</subject><ispartof>Macromolecules, 2013-07, Vol.46 (13), p.5279-5289</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a316t-13d5d678e7bb8e85a97bcfa8d4a59e7ceaf4ea950aa71d5871d484a61ec32d0f3</citedby><cites>FETCH-LOGICAL-a316t-13d5d678e7bb8e85a97bcfa8d4a59e7ceaf4ea950aa71d5871d484a61ec32d0f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ma4005007$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma4005007$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,776,780,881,2751,27055,27903,27904,56717,56767</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27561748$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1110076$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Che, Justin</creatorcontrib><creatorcontrib>Locker, C. Rebecca</creatorcontrib><creatorcontrib>Lee, Sanghun</creatorcontrib><creatorcontrib>Rutledge, Gregory C</creatorcontrib><creatorcontrib>Hsiao, Benjamin S</creatorcontrib><creatorcontrib>Tsou, Andy H</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL)</creatorcontrib><title>Plastic Deformation of Semicrystalline Polyethylene by X‑ray Scattering: Comparison with Atomistic Simulations</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Plastic deformation of uniaxially oriented polyethylene (PE) fiber has been examined by small and wide angle synchrotron X-ray scattering. Morphology changes of the lamellar stack with deformation beyond yielding have been characterized and quantified. Atomistic simulations of tensile deformation of the lamellar stack in the longitudinal direction compare favorably to the experimentally observed morphological changes in the PE fiber. Experimental deformations at 100 °C exhibit responses comparable to those observed by simulation of deformation with constant total volume at 77 °C and a strain rate of 5 × 106 s–1. Experimental deformations of the PE fiber at 25 °C were found to be comparable to simulated tensile deformation with constant lateral dimensions at 77 °C and a strain rate of 5 × 107 s–1. Cavitation in the interlamellar region was found experimentally in the PE fiber deforming at room temperature as predicted by simulation with constant lateral dimensions at the higher strain rate. Melting, recrystallization, and removal of entanglements observed in the PE fiber deformation at 100 °C agree with the simulation results of a constant volume deformation at the slower strain rate. The ability to define the deformation behavior of PE at room and at high temperatures through simulation offers unique opportunities to examine how the interlamellar amorphous topology affects PE deformation.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Fibers and threads</subject><subject>Forms of application and semi-finished materials</subject><subject>Polymer industry, paints, wood</subject><subject>Technology of polymers</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNptkM9KxDAQh4MouK4efIMgePBQTdqmSb0t619YcGEVvJVpmrhZ2qYkWaQ3X8FX9Emsu7JevMww8M3HzA-hU0ouKYnpVQMpIYwQvodGlMUkYiJh-2hESJxGeZzzQ3Tk_YoQSlmajFA3r8EHI_GN0tY1EIxtsdV4oRojXe8D1LVpFZ7buldh2ddqGMoev359fDro8UJCCMqZ9u0aT23TgTN-MLybsMSTYBuzkS9Ms643bn-MDjTUXp389jF6ubt9nj5Es6f7x-lkFkFCsxDRpGJVxoXiZSmUYJDzUmoQVQosV1wq0KmCnBEATismhpKKFDKqZBJXRCdjdLb12uGCwksTlFxK27ZKhoJSOkSUDdDFFpLOeu-ULjpnGnB9QUnxk2exy3Ngz7dsB15CrR200vjdQsxZRnkq_jiQvljZtWuHN__xfQMcVIPv</recordid><startdate>20130709</startdate><enddate>20130709</enddate><creator>Che, Justin</creator><creator>Locker, C. Rebecca</creator><creator>Lee, Sanghun</creator><creator>Rutledge, Gregory C</creator><creator>Hsiao, Benjamin S</creator><creator>Tsou, Andy H</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20130709</creationdate><title>Plastic Deformation of Semicrystalline Polyethylene by X‑ray Scattering: Comparison with Atomistic Simulations</title><author>Che, Justin ; Locker, C. Rebecca ; Lee, Sanghun ; Rutledge, Gregory C ; Hsiao, Benjamin S ; Tsou, Andy H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a316t-13d5d678e7bb8e85a97bcfa8d4a59e7ceaf4ea950aa71d5871d484a61ec32d0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Fibers and threads</topic><topic>Forms of application and semi-finished materials</topic><topic>Polymer industry, paints, wood</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Che, Justin</creatorcontrib><creatorcontrib>Locker, C. Rebecca</creatorcontrib><creatorcontrib>Lee, Sanghun</creatorcontrib><creatorcontrib>Rutledge, Gregory C</creatorcontrib><creatorcontrib>Hsiao, Benjamin S</creatorcontrib><creatorcontrib>Tsou, Andy H</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL)</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Che, Justin</au><au>Locker, C. Rebecca</au><au>Lee, Sanghun</au><au>Rutledge, Gregory C</au><au>Hsiao, Benjamin S</au><au>Tsou, Andy H</au><aucorp>Brookhaven National Laboratory (BNL)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plastic Deformation of Semicrystalline Polyethylene by X‑ray Scattering: Comparison with Atomistic Simulations</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2013-07-09</date><risdate>2013</risdate><volume>46</volume><issue>13</issue><spage>5279</spage><epage>5289</epage><pages>5279-5289</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>Plastic deformation of uniaxially oriented polyethylene (PE) fiber has been examined by small and wide angle synchrotron X-ray scattering. Morphology changes of the lamellar stack with deformation beyond yielding have been characterized and quantified. Atomistic simulations of tensile deformation of the lamellar stack in the longitudinal direction compare favorably to the experimentally observed morphological changes in the PE fiber. Experimental deformations at 100 °C exhibit responses comparable to those observed by simulation of deformation with constant total volume at 77 °C and a strain rate of 5 × 106 s–1. Experimental deformations of the PE fiber at 25 °C were found to be comparable to simulated tensile deformation with constant lateral dimensions at 77 °C and a strain rate of 5 × 107 s–1. Cavitation in the interlamellar region was found experimentally in the PE fiber deforming at room temperature as predicted by simulation with constant lateral dimensions at the higher strain rate. Melting, recrystallization, and removal of entanglements observed in the PE fiber deformation at 100 °C agree with the simulation results of a constant volume deformation at the slower strain rate. The ability to define the deformation behavior of PE at room and at high temperatures through simulation offers unique opportunities to examine how the interlamellar amorphous topology affects PE deformation.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma4005007</doi><tpages>11</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology Fibers and threads Forms of application and semi-finished materials Polymer industry, paints, wood Technology of polymers |
title | Plastic Deformation of Semicrystalline Polyethylene by X‑ray Scattering: Comparison with Atomistic Simulations |
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