Pressure and Temperature Dependence of the Dilute Solution Segmental Dynamics of Anthracene-Labeled Polyisoprene
The local segmental dynamics of anthracene-labeled cis-1,4-polyisoprene in dilute solution have been studied as a function of temperature (298−323 K) and pressure (0.1−150 MPa) in several solvents (dioctyl phthalate, n-dodecane, squalane, and toluene). This range of temperature and pressure afforded...
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Veröffentlicht in: | Macromolecules 2002-04, Vol.35 (8), p.3281-3287 |
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description | The local segmental dynamics of anthracene-labeled cis-1,4-polyisoprene in dilute solution have been studied as a function of temperature (298−323 K) and pressure (0.1−150 MPa) in several solvents (dioctyl phthalate, n-dodecane, squalane, and toluene). This range of temperature and pressure afforded a viscosity range of 0.55−494 mPa·s. Previous studies of cis-1,4-polyisoprene as a function of temperature at ambient pressure have revealed that these motions scale as a fractional power of the solvent viscosity, η, thereby violating Kramers' theory which predicts τ c ∼ η. Findings reveal quantitatively similar behavior is observed when the solvent viscosity is varied by pressure at fixed temperatures. |
doi_str_mv | 10.1021/ma011783r |
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J ; Adolf, D. B</creator><creatorcontrib>Punchard, B. J ; Adolf, D. B</creatorcontrib><description>The local segmental dynamics of anthracene-labeled cis-1,4-polyisoprene in dilute solution have been studied as a function of temperature (298−323 K) and pressure (0.1−150 MPa) in several solvents (dioctyl phthalate, n-dodecane, squalane, and toluene). This range of temperature and pressure afforded a viscosity range of 0.55−494 mPa·s. Previous studies of cis-1,4-polyisoprene as a function of temperature at ambient pressure have revealed that these motions scale as a fractional power of the solvent viscosity, η, thereby violating Kramers' theory which predicts τ c ∼ η. Findings reveal quantitatively similar behavior is observed when the solvent viscosity is varied by pressure at fixed temperatures.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma011783r</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Exact sciences and technology ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization ; Solution and gel properties</subject><ispartof>Macromolecules, 2002-04, Vol.35 (8), p.3281-3287</ispartof><rights>Copyright © 2002 American Chemical Society</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a325t-a99c7d766114e26e6d2c7a3e6b26b0288c54e325b2bbb1e4c273abe739354cce3</citedby><cites>FETCH-LOGICAL-a325t-a99c7d766114e26e6d2c7a3e6b26b0288c54e325b2bbb1e4c273abe739354cce3</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/ma011783r$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ma011783r$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13628017$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Punchard, B. 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Findings reveal quantitatively similar behavior is observed when the solvent viscosity is varied by pressure at fixed temperatures.</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Solution and gel properties</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNptkE9PwkAQxTdGExE9-A168eChun-63fZIRMQEIxE8b6bbQYrtttktiXx7l2Dg4ullZn7zXmYIuWX0gVHOHhugjKlMuDMyYJLTWGZCnpMBpTyJc56rS3Ll_YYGSiZiQLq5Q--3DiOwZbTEpkMH_b4eY4e2RGswaldRvw6dqt72GC3aIFVrowV-NWh7qKPxzkJTGb8nR7ZfOzBoMZ5BgTWW0bytd5VvOxea1-RiBbXHmz8dks_J8_JpGs_eX16fRrMYBJd9DHluVKnSlLEEeYppyY0CgWnB04LyLDMywUAWvCgKhonhSoQ0JXIhE2NQDMn9wde41nuHK925qgG304zq_av08VWBvTuwHXgD9cqBNZU_LYiUZ5SpwMUHrvI9_hzn4L51qoSSejlf6LGcThYfbKrfTr5gvN60W2fDxf_k_wKMhIWv</recordid><startdate>20020409</startdate><enddate>20020409</enddate><creator>Punchard, B. 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B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pressure and Temperature Dependence of the Dilute Solution Segmental Dynamics of Anthracene-Labeled Polyisoprene</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2002-04-09</date><risdate>2002</risdate><volume>35</volume><issue>8</issue><spage>3281</spage><epage>3287</epage><pages>3281-3287</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>The local segmental dynamics of anthracene-labeled cis-1,4-polyisoprene in dilute solution have been studied as a function of temperature (298−323 K) and pressure (0.1−150 MPa) in several solvents (dioctyl phthalate, n-dodecane, squalane, and toluene). This range of temperature and pressure afforded a viscosity range of 0.55−494 mPa·s. Previous studies of cis-1,4-polyisoprene as a function of temperature at ambient pressure have revealed that these motions scale as a fractional power of the solvent viscosity, η, thereby violating Kramers' theory which predicts τ c ∼ η. Findings reveal quantitatively similar behavior is observed when the solvent viscosity is varied by pressure at fixed temperatures.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma011783r</doi><tpages>7</tpages></addata></record> |
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title | Pressure and Temperature Dependence of the Dilute Solution Segmental Dynamics of Anthracene-Labeled Polyisoprene |
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