Enthalpy recovery of ultrathin polystyrene film using Flash DSC
Enthalpy recovery for a single polystyrene ultrathin film of 20 nm thickness is studied using Flash DSC over an extended time and temperature range. Results are compared to a bulk sample of the same polystyrene using a similar experimental protocol and analysis procedure in an effort to determine th...
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description | Enthalpy recovery for a single polystyrene ultrathin film of 20 nm thickness is studied using Flash DSC over an extended time and temperature range. Results are compared to a bulk sample of the same polystyrene using a similar experimental protocol and analysis procedure in an effort to determine the effects of nanoconfinement. Examined is the cooling rate dependence of the glass transition temperature (Tg) of unaged films which informs the initial fictive temperature (Tfo) and thus the jump size (Tfo - Ta) for a given aging temperature (Ta). Isothermal enthalpy recovery is investigated as a function of both Ta for various cooling rates and as a function of jump size at constant Ta. The apparent activation energies at Tg and along the glassy line are determined and compared, as is the enthalpy recovery aging rate. Although the apparent activation energy along the glass line is the same within experimental error as the bulk, the aging rate is found to be slightly faster in the ultrathin film. Increasing the cooling rate prior to aging increases the aging rate. The results are discussed in the context of the two competing factors which influence the aging rate, namely, the driving force and the molecular mobility. The driving force for aging is dictated by the jump size or cooling rate, i.e., the value of Tfo - Ta. The mobility, on the other hand, is dictated by the relaxation time at the aging temperature, which increases during aging from the value on the initial glass line to that at equilibrium. The initial mobility in the glassy state is dictated by the jump size, being related to Tfo - Ta and the temperature dependence of the relaxation time along the glass line, whereas the mobility at equilibrium is dictated by Ta, Tg, and the temperature dependence and breadth of the equilibrium relaxation time.
[Display omitted]
•Enthalpy recovery for a 20 nm thick polystyrene is studied using Flash DSC.•Compared to bulk, the thin film has a broader and depressed Tg.•The thin film shows no aging for several conditions where aging occurs for the bulk.•The aging rate depends on two competing factors: jump size and aging temperature.•The aging rate is faster for the thin film at temperatures between 60 and 100 °C. |
doi_str_mv | 10.1016/j.polymer.2018.02.038 |
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[Display omitted]
•Enthalpy recovery for a 20 nm thick polystyrene is studied using Flash DSC.•Compared to bulk, the thin film has a broader and depressed Tg.•The thin film shows no aging for several conditions where aging occurs for the bulk.•The aging rate depends on two competing factors: jump size and aging temperature.•The aging rate is faster for the thin film at temperatures between 60 and 100 °C.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2018.02.038</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Activation energy ; Aging ; Cooling ; Cooling rate ; Differential scanning calorimetry ; Enthalpy ; Enthalpy recovery ; Glass transition temperature ; Heating ; Mobility ; Molecular chains ; Polystyrene ; Polystyrene resins ; Recovery ; Relaxation time ; Temperature dependence ; Temperature effects ; Thermodynamics ; Thickness ; Thin films ; Time dependence ; Transition temperatures ; Ultrathin film</subject><ispartof>Polymer (Guilford), 2018-05, Vol.143, p.40-45</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright Elsevier BV May 9, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-f74c23e1c49b1c62fd03d353a094ee9f67c18b1f98b4b3010a76d561bd2e20403</citedby><cites>FETCH-LOGICAL-c421t-f74c23e1c49b1c62fd03d353a094ee9f67c18b1f98b4b3010a76d561bd2e20403</cites><orcidid>0000-0001-7498-2826</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0032386118301630$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Koh, Yung P.</creatorcontrib><creatorcontrib>Simon, Sindee L.</creatorcontrib><title>Enthalpy recovery of ultrathin polystyrene film using Flash DSC</title><title>Polymer (Guilford)</title><description>Enthalpy recovery for a single polystyrene ultrathin film of 20 nm thickness is studied using Flash DSC over an extended time and temperature range. Results are compared to a bulk sample of the same polystyrene using a similar experimental protocol and analysis procedure in an effort to determine the effects of nanoconfinement. Examined is the cooling rate dependence of the glass transition temperature (Tg) of unaged films which informs the initial fictive temperature (Tfo) and thus the jump size (Tfo - Ta) for a given aging temperature (Ta). Isothermal enthalpy recovery is investigated as a function of both Ta for various cooling rates and as a function of jump size at constant Ta. The apparent activation energies at Tg and along the glassy line are determined and compared, as is the enthalpy recovery aging rate. Although the apparent activation energy along the glass line is the same within experimental error as the bulk, the aging rate is found to be slightly faster in the ultrathin film. Increasing the cooling rate prior to aging increases the aging rate. The results are discussed in the context of the two competing factors which influence the aging rate, namely, the driving force and the molecular mobility. The driving force for aging is dictated by the jump size or cooling rate, i.e., the value of Tfo - Ta. The mobility, on the other hand, is dictated by the relaxation time at the aging temperature, which increases during aging from the value on the initial glass line to that at equilibrium. The initial mobility in the glassy state is dictated by the jump size, being related to Tfo - Ta and the temperature dependence of the relaxation time along the glass line, whereas the mobility at equilibrium is dictated by Ta, Tg, and the temperature dependence and breadth of the equilibrium relaxation time.
[Display omitted]
•Enthalpy recovery for a 20 nm thick polystyrene is studied using Flash DSC.•Compared to bulk, the thin film has a broader and depressed Tg.•The thin film shows no aging for several conditions where aging occurs for the bulk.•The aging rate depends on two competing factors: jump size and aging temperature.•The aging rate is faster for the thin film at temperatures between 60 and 100 °C.</description><subject>Activation energy</subject><subject>Aging</subject><subject>Cooling</subject><subject>Cooling rate</subject><subject>Differential scanning calorimetry</subject><subject>Enthalpy</subject><subject>Enthalpy recovery</subject><subject>Glass transition temperature</subject><subject>Heating</subject><subject>Mobility</subject><subject>Molecular chains</subject><subject>Polystyrene</subject><subject>Polystyrene resins</subject><subject>Recovery</subject><subject>Relaxation time</subject><subject>Temperature dependence</subject><subject>Temperature effects</subject><subject>Thermodynamics</subject><subject>Thickness</subject><subject>Thin films</subject><subject>Time dependence</subject><subject>Transition temperatures</subject><subject>Ultrathin film</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkMFKxDAQhoMouK4-ghDw3DqTpG16WmTdVWHBg3oObZq4Kd22Ju1C394u693THOb_v2E-Qu4RYgRMH-u475rpYHzMAGUMLAYuL8gCZcYjxnK8JAsAziIuU7wmNyHUAMASJhZktWmHfdH0E_VGd0fjJ9pZOjaDL4a9a-mJHIbJm9ZQ65oDHYNrv-m2KcKePn-sb8mVLZpg7v7mknxtN5_r12j3_vK2ftpFWjAcIpsJzbhBLfISdcpsBbziCS8gF8bkNs00yhJtLktRckAosrRKUiwrZhgI4EvycOb2vvsZTRhU3Y2-nU8qBqkUUrIkm1PJOaV9F4I3VvXeHQo_KQR1cqVq9edKnVwpYGp2NfdW556ZXzi6eRu0M602lZu1DKrq3D-EX6xLdLw</recordid><startdate>20180509</startdate><enddate>20180509</enddate><creator>Koh, Yung P.</creator><creator>Simon, Sindee L.</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0001-7498-2826</orcidid></search><sort><creationdate>20180509</creationdate><title>Enthalpy recovery of ultrathin polystyrene film using Flash DSC</title><author>Koh, Yung P. ; Simon, Sindee L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-f74c23e1c49b1c62fd03d353a094ee9f67c18b1f98b4b3010a76d561bd2e20403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Activation energy</topic><topic>Aging</topic><topic>Cooling</topic><topic>Cooling rate</topic><topic>Differential scanning calorimetry</topic><topic>Enthalpy</topic><topic>Enthalpy recovery</topic><topic>Glass transition temperature</topic><topic>Heating</topic><topic>Mobility</topic><topic>Molecular chains</topic><topic>Polystyrene</topic><topic>Polystyrene resins</topic><topic>Recovery</topic><topic>Relaxation time</topic><topic>Temperature dependence</topic><topic>Temperature effects</topic><topic>Thermodynamics</topic><topic>Thickness</topic><topic>Thin films</topic><topic>Time dependence</topic><topic>Transition temperatures</topic><topic>Ultrathin film</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koh, Yung P.</creatorcontrib><creatorcontrib>Simon, Sindee L.</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koh, Yung P.</au><au>Simon, Sindee L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enthalpy recovery of ultrathin polystyrene film using Flash DSC</atitle><jtitle>Polymer (Guilford)</jtitle><date>2018-05-09</date><risdate>2018</risdate><volume>143</volume><spage>40</spage><epage>45</epage><pages>40-45</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><abstract>Enthalpy recovery for a single polystyrene ultrathin film of 20 nm thickness is studied using Flash DSC over an extended time and temperature range. Results are compared to a bulk sample of the same polystyrene using a similar experimental protocol and analysis procedure in an effort to determine the effects of nanoconfinement. Examined is the cooling rate dependence of the glass transition temperature (Tg) of unaged films which informs the initial fictive temperature (Tfo) and thus the jump size (Tfo - Ta) for a given aging temperature (Ta). Isothermal enthalpy recovery is investigated as a function of both Ta for various cooling rates and as a function of jump size at constant Ta. The apparent activation energies at Tg and along the glassy line are determined and compared, as is the enthalpy recovery aging rate. Although the apparent activation energy along the glass line is the same within experimental error as the bulk, the aging rate is found to be slightly faster in the ultrathin film. Increasing the cooling rate prior to aging increases the aging rate. The results are discussed in the context of the two competing factors which influence the aging rate, namely, the driving force and the molecular mobility. The driving force for aging is dictated by the jump size or cooling rate, i.e., the value of Tfo - Ta. The mobility, on the other hand, is dictated by the relaxation time at the aging temperature, which increases during aging from the value on the initial glass line to that at equilibrium. The initial mobility in the glassy state is dictated by the jump size, being related to Tfo - Ta and the temperature dependence of the relaxation time along the glass line, whereas the mobility at equilibrium is dictated by Ta, Tg, and the temperature dependence and breadth of the equilibrium relaxation time.
[Display omitted]
•Enthalpy recovery for a 20 nm thick polystyrene is studied using Flash DSC.•Compared to bulk, the thin film has a broader and depressed Tg.•The thin film shows no aging for several conditions where aging occurs for the bulk.•The aging rate depends on two competing factors: jump size and aging temperature.•The aging rate is faster for the thin film at temperatures between 60 and 100 °C.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2018.02.038</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-7498-2826</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Activation energy Aging Cooling Cooling rate Differential scanning calorimetry Enthalpy Enthalpy recovery Glass transition temperature Heating Mobility Molecular chains Polystyrene Polystyrene resins Recovery Relaxation time Temperature dependence Temperature effects Thermodynamics Thickness Thin films Time dependence Transition temperatures Ultrathin film |
title | Enthalpy recovery of ultrathin polystyrene film using Flash DSC |
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