Surface tension of mixtures of oligomers
The surface tension of mixtures of poly(dimethylsiloxane) and poly(isobutylene) fluids with their low molecular weight oligomers have been measured. These data, as well as those for n‐alkane mixtures from the literature, are fitted well by lattice‐theory expressions for the surface tension of polyme...
Gespeichert in:
| Veröffentlicht in: | Journal of polymer science. Part C, Polymer symposia Polymer symposia, 1971, Vol.34 (1), p.45-51 |
|---|---|
| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 51 |
|---|---|
| container_issue | 1 |
| container_start_page | 45 |
| container_title | Journal of polymer science. Part C, Polymer symposia |
| container_volume | 34 |
| creator | Legrand, D. G. Gaines Jr, G. L. |
| description | The surface tension of mixtures of poly(dimethylsiloxane) and poly(isobutylene) fluids with their low molecular weight oligomers have been measured. These data, as well as those for n‐alkane mixtures from the literature, are fitted well by lattice‐theory expressions for the surface tension of polymer solutions, and do not show a simple dependence on the average molecular weight in the mixture. We conclude that the molecular weight depend‐ence we have previously observed for the surface tension of polymer fluids is only an approximation. The results also suggest that the lattice‐model theory may have broader applicability than the model from which it was developed would imply. |
| doi_str_mv | 10.1002/polc.5070340107 |
| format | Article |
| fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_polc_5070340107</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_LFZCLWS7_F</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1767-de7ded65670b19e0dc08d807fa1b6971c916cb63c4e5eb424f0f3142705c6e503</originalsourceid><addsrcrecordid>eNqFz01Lw0AQgOFFFKzVs9cevaSdzX5MF08SbBWCFaoUvCzJZlaiaVN2U2z_vZaK4snTzGGegZexSw5DDpCO1m3jhgoQhAQOeMR63AiVCNDqmPVASpOkxshTdhbjG4BODeoeu5pvgi8cDTpaxbpdDVo_WNbbbhMo7ve2qV_bJYV4zk580US6-J599jy5fcruknw2vc9u8sRx1JhUhBVVWmmEkhuCysG4GgP6gpfaIHeGa1dq4SQpKmUqPXjBZYqgnCYFos9Gh78utDEG8nYd6mURdpaD3Yfafaj9Df0S1wfxUTe0--_cPs7y7I9ODrqOHW1_dBHerUaByi4epjafvGT5Yo52Ij4B94lmzA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Surface tension of mixtures of oligomers</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Legrand, D. G. ; Gaines Jr, G. L.</creator><creatorcontrib>Legrand, D. G. ; Gaines Jr, G. L.</creatorcontrib><description>The surface tension of mixtures of poly(dimethylsiloxane) and poly(isobutylene) fluids with their low molecular weight oligomers have been measured. These data, as well as those for n‐alkane mixtures from the literature, are fitted well by lattice‐theory expressions for the surface tension of polymer solutions, and do not show a simple dependence on the average molecular weight in the mixture. We conclude that the molecular weight depend‐ence we have previously observed for the surface tension of polymer fluids is only an approximation. The results also suggest that the lattice‐model theory may have broader applicability than the model from which it was developed would imply.</description><identifier>ISSN: 0449-2994</identifier><identifier>EISSN: 1935-3065</identifier><identifier>DOI: 10.1002/polc.5070340107</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><ispartof>Journal of polymer science. Part C, Polymer symposia, 1971, Vol.34 (1), p.45-51</ispartof><rights>Copyright © 1971 Wiley Periodicals, Inc., A Wiley Company</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1767-de7ded65670b19e0dc08d807fa1b6971c916cb63c4e5eb424f0f3142705c6e503</citedby><cites>FETCH-LOGICAL-c1767-de7ded65670b19e0dc08d807fa1b6971c916cb63c4e5eb424f0f3142705c6e503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpolc.5070340107$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpolc.5070340107$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Legrand, D. G.</creatorcontrib><creatorcontrib>Gaines Jr, G. L.</creatorcontrib><title>Surface tension of mixtures of oligomers</title><title>Journal of polymer science. Part C, Polymer symposia</title><addtitle>J. polym. sci., C Polym. symp</addtitle><description>The surface tension of mixtures of poly(dimethylsiloxane) and poly(isobutylene) fluids with their low molecular weight oligomers have been measured. These data, as well as those for n‐alkane mixtures from the literature, are fitted well by lattice‐theory expressions for the surface tension of polymer solutions, and do not show a simple dependence on the average molecular weight in the mixture. We conclude that the molecular weight depend‐ence we have previously observed for the surface tension of polymer fluids is only an approximation. The results also suggest that the lattice‐model theory may have broader applicability than the model from which it was developed would imply.</description><issn>0449-2994</issn><issn>1935-3065</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1971</creationdate><recordtype>article</recordtype><recordid>eNqFz01Lw0AQgOFFFKzVs9cevaSdzX5MF08SbBWCFaoUvCzJZlaiaVN2U2z_vZaK4snTzGGegZexSw5DDpCO1m3jhgoQhAQOeMR63AiVCNDqmPVASpOkxshTdhbjG4BODeoeu5pvgi8cDTpaxbpdDVo_WNbbbhMo7ve2qV_bJYV4zk580US6-J599jy5fcruknw2vc9u8sRx1JhUhBVVWmmEkhuCysG4GgP6gpfaIHeGa1dq4SQpKmUqPXjBZYqgnCYFos9Gh78utDEG8nYd6mURdpaD3Yfafaj9Df0S1wfxUTe0--_cPs7y7I9ODrqOHW1_dBHerUaByi4epjafvGT5Yo52Ij4B94lmzA</recordid><startdate>1971</startdate><enddate>1971</enddate><creator>Legrand, D. G.</creator><creator>Gaines Jr, G. L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1971</creationdate><title>Surface tension of mixtures of oligomers</title><author>Legrand, D. G. ; Gaines Jr, G. L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1767-de7ded65670b19e0dc08d807fa1b6971c916cb63c4e5eb424f0f3142705c6e503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1971</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Legrand, D. G.</creatorcontrib><creatorcontrib>Gaines Jr, G. L.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of polymer science. Part C, Polymer symposia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Legrand, D. G.</au><au>Gaines Jr, G. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface tension of mixtures of oligomers</atitle><jtitle>Journal of polymer science. Part C, Polymer symposia</jtitle><addtitle>J. polym. sci., C Polym. symp</addtitle><date>1971</date><risdate>1971</risdate><volume>34</volume><issue>1</issue><spage>45</spage><epage>51</epage><pages>45-51</pages><issn>0449-2994</issn><eissn>1935-3065</eissn><abstract>The surface tension of mixtures of poly(dimethylsiloxane) and poly(isobutylene) fluids with their low molecular weight oligomers have been measured. These data, as well as those for n‐alkane mixtures from the literature, are fitted well by lattice‐theory expressions for the surface tension of polymer solutions, and do not show a simple dependence on the average molecular weight in the mixture. We conclude that the molecular weight depend‐ence we have previously observed for the surface tension of polymer fluids is only an approximation. The results also suggest that the lattice‐model theory may have broader applicability than the model from which it was developed would imply.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/polc.5070340107</doi><tpages>7</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0449-2994 |
| ispartof | Journal of polymer science. Part C, Polymer symposia, 1971, Vol.34 (1), p.45-51 |
| issn | 0449-2994 1935-3065 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_polc_5070340107 |
| source | Wiley Online Library Journals Frontfile Complete |
| title | Surface tension of mixtures of oligomers |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T05%3A09%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Surface%20tension%20of%20mixtures%20of%20oligomers&rft.jtitle=Journal%20of%20polymer%20science.%20Part%20C,%20Polymer%20symposia&rft.au=Legrand,%20D.%20G.&rft.date=1971&rft.volume=34&rft.issue=1&rft.spage=45&rft.epage=51&rft.pages=45-51&rft.issn=0449-2994&rft.eissn=1935-3065&rft_id=info:doi/10.1002/polc.5070340107&rft_dat=%3Cistex_cross%3Eark_67375_WNG_LFZCLWS7_F%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |