Rapid formation of soft hydrophilic silicone elastomer surfaces
We report on the rapid formation of hydrophilic silicone elastomer surfaces by ultraviolet/ozone (UVO) irradiation of poly(vinylmethyl siloxane) (PVMS) network films. Our results reveal that the PVMS network surfaces render hydrophilic upon only a short UVO exposure time (seconds to a few minutes)....
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Veröffentlicht in: | Polymer (Guilford) 2005-10, Vol.46 (22), p.9329-9341 |
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creator | Efimenko, Kirill Crowe, Julie A. Manias, Evangelos Schwark, Dwight W. Fischer, Daniel A. Genzer, Jan |
description | We report on the rapid formation of hydrophilic silicone elastomer surfaces by ultraviolet/ozone (UVO) irradiation of poly(vinylmethyl siloxane) (PVMS) network films. Our results reveal that the PVMS network surfaces render hydrophilic upon only a short UVO exposure time (seconds to a few minutes). We also provide evidence that the brief UVO irradiation treatment does not cause dramatic changes in the surface modulus of the PVMS network. We compare the rate of formation of hydrophilic silicone elastomer surfaces made of PVMS to those of model poly(dimethyl siloxane) (PDMS) and commercial-grade PDMS (Sylgard-184). We find that relative to PVMS, 20 times longer UVO treatment times are needed to oxidize the PDMS network surfaces in order to achieve a comparable density of surface-bound hydrophilic moieties. The longer UVO treatment times for PDMS are in turn responsible for the dramatic increase in surface modulus of UVO treated PDMS, relative to PVMS. We also study the formation of self-assembled monolayers (SAMs) made of semifluorinated organosilane precursors on the PVMS-UVO and PDMS-UVO network surfaces. By tuning the UVO treatment times and by utilizing mono- and tri-functional organosilanes we find that while mono-functionalized organosilanes attach directly to the substrate, SAMs of tri-functionalized organosilanes form in-plane networks on the underlying UVO-modified silicone elastomer surface, even with only short UVO exposure times. |
doi_str_mv | 10.1016/j.polymer.2005.07.046 |
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Our results reveal that the PVMS network surfaces render hydrophilic upon only a short UVO exposure time (seconds to a few minutes). We also provide evidence that the brief UVO irradiation treatment does not cause dramatic changes in the surface modulus of the PVMS network. We compare the rate of formation of hydrophilic silicone elastomer surfaces made of PVMS to those of model poly(dimethyl siloxane) (PDMS) and commercial-grade PDMS (Sylgard-184). We find that relative to PVMS, 20 times longer UVO treatment times are needed to oxidize the PDMS network surfaces in order to achieve a comparable density of surface-bound hydrophilic moieties. The longer UVO treatment times for PDMS are in turn responsible for the dramatic increase in surface modulus of UVO treated PDMS, relative to PVMS. We also study the formation of self-assembled monolayers (SAMs) made of semifluorinated organosilane precursors on the PVMS-UVO and PDMS-UVO network surfaces. By tuning the UVO treatment times and by utilizing mono- and tri-functional organosilanes we find that while mono-functionalized organosilanes attach directly to the substrate, SAMs of tri-functionalized organosilanes form in-plane networks on the underlying UVO-modified silicone elastomer surface, even with only short UVO exposure times.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2005.07.046</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Coating, metallization, dyeing ; ELASTOMERS ; Exact sciences and technology ; Functionalized silicone rubber ; IRRADIATION ; Machinery and processing ; MATERIALS SCIENCE ; national synchrotron light source ; OZONE ; Plastics ; Polymer industry, paints, wood ; Self-assembly ; SILANES ; SILICONES ; Surface modification ; SURFACES ; Technology of polymers ; ULTRAVIOLET RADIATION</subject><ispartof>Polymer (Guilford), 2005-10, Vol.46 (22), p.9329-9341</ispartof><rights>2005 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-8532d88a65d566f74cb94bfd1d2f4b812057c3b1b357bfbcdf230cb5f2dc80163</citedby><cites>FETCH-LOGICAL-c458t-8532d88a65d566f74cb94bfd1d2f4b812057c3b1b357bfbcdf230cb5f2dc80163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.polymer.2005.07.046$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17146913$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/913668$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Efimenko, Kirill</creatorcontrib><creatorcontrib>Crowe, Julie A.</creatorcontrib><creatorcontrib>Manias, Evangelos</creatorcontrib><creatorcontrib>Schwark, Dwight W.</creatorcontrib><creatorcontrib>Fischer, Daniel A.</creatorcontrib><creatorcontrib>Genzer, Jan</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL) National Synchrotron Light Source</creatorcontrib><title>Rapid formation of soft hydrophilic silicone elastomer surfaces</title><title>Polymer (Guilford)</title><description>We report on the rapid formation of hydrophilic silicone elastomer surfaces by ultraviolet/ozone (UVO) irradiation of poly(vinylmethyl siloxane) (PVMS) network films. Our results reveal that the PVMS network surfaces render hydrophilic upon only a short UVO exposure time (seconds to a few minutes). We also provide evidence that the brief UVO irradiation treatment does not cause dramatic changes in the surface modulus of the PVMS network. We compare the rate of formation of hydrophilic silicone elastomer surfaces made of PVMS to those of model poly(dimethyl siloxane) (PDMS) and commercial-grade PDMS (Sylgard-184). We find that relative to PVMS, 20 times longer UVO treatment times are needed to oxidize the PDMS network surfaces in order to achieve a comparable density of surface-bound hydrophilic moieties. The longer UVO treatment times for PDMS are in turn responsible for the dramatic increase in surface modulus of UVO treated PDMS, relative to PVMS. We also study the formation of self-assembled monolayers (SAMs) made of semifluorinated organosilane precursors on the PVMS-UVO and PDMS-UVO network surfaces. By tuning the UVO treatment times and by utilizing mono- and tri-functional organosilanes we find that while mono-functionalized organosilanes attach directly to the substrate, SAMs of tri-functionalized organosilanes form in-plane networks on the underlying UVO-modified silicone elastomer surface, even with only short UVO exposure times.</description><subject>Applied sciences</subject><subject>Coating, metallization, dyeing</subject><subject>ELASTOMERS</subject><subject>Exact sciences and technology</subject><subject>Functionalized silicone rubber</subject><subject>IRRADIATION</subject><subject>Machinery and processing</subject><subject>MATERIALS SCIENCE</subject><subject>national synchrotron light source</subject><subject>OZONE</subject><subject>Plastics</subject><subject>Polymer industry, paints, wood</subject><subject>Self-assembly</subject><subject>SILANES</subject><subject>SILICONES</subject><subject>Surface modification</subject><subject>SURFACES</subject><subject>Technology of polymers</subject><subject>ULTRAVIOLET RADIATION</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkU9r3DAQxUVoIdu0HyHgHJqbnZFkyfIphJA2gUAgtGch6w-rxWu5Gm9gv3217EKOyWXm8pt5M-8RckmhoUDlzaaZ07jf-twwANFA10Arz8iKqo7XjPX0C1kBcFZzJek5-Ya4AQAmWLsit69mjq4KKW_NEtNUpVBhCku13ruc5nUco63wUNPkKz8aXFJRqnCXg7Eev5OvwYzof5z6Bfn76-HP_WP9_PL76f7uubatUEutBGdOKSOFE1KGrrVD3w7BUcdCOyjKQHSWD3TgohvCYF1gHOwgAnNWlR_5Bbk67k24RI02Lt6uy02Tt4vuKZdSFeb6yMw5_dt5XPQ2ovXjaCafdqhZLxRw9QlQKRBS9J8AZSs47woojqDNCTH7oOcctybvNQV9CElv9CkkfQhJQ6dLSGXu50nAoDVjyGayEd-HO9rK8l3hbo-cLx6_xbKlWOAn613MBwdcih8o_Qe1rapz</recordid><startdate>20051024</startdate><enddate>20051024</enddate><creator>Efimenko, Kirill</creator><creator>Crowe, Julie A.</creator><creator>Manias, Evangelos</creator><creator>Schwark, Dwight W.</creator><creator>Fischer, Daniel A.</creator><creator>Genzer, Jan</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>F28</scope><scope>FR3</scope><scope>7TB</scope><scope>OTOTI</scope></search><sort><creationdate>20051024</creationdate><title>Rapid formation of soft hydrophilic silicone elastomer surfaces</title><author>Efimenko, Kirill ; 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Our results reveal that the PVMS network surfaces render hydrophilic upon only a short UVO exposure time (seconds to a few minutes). We also provide evidence that the brief UVO irradiation treatment does not cause dramatic changes in the surface modulus of the PVMS network. We compare the rate of formation of hydrophilic silicone elastomer surfaces made of PVMS to those of model poly(dimethyl siloxane) (PDMS) and commercial-grade PDMS (Sylgard-184). We find that relative to PVMS, 20 times longer UVO treatment times are needed to oxidize the PDMS network surfaces in order to achieve a comparable density of surface-bound hydrophilic moieties. The longer UVO treatment times for PDMS are in turn responsible for the dramatic increase in surface modulus of UVO treated PDMS, relative to PVMS. We also study the formation of self-assembled monolayers (SAMs) made of semifluorinated organosilane precursors on the PVMS-UVO and PDMS-UVO network surfaces. By tuning the UVO treatment times and by utilizing mono- and tri-functional organosilanes we find that while mono-functionalized organosilanes attach directly to the substrate, SAMs of tri-functionalized organosilanes form in-plane networks on the underlying UVO-modified silicone elastomer surface, even with only short UVO exposure times.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2005.07.046</doi><tpages>13</tpages></addata></record> |
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subjects | Applied sciences Coating, metallization, dyeing ELASTOMERS Exact sciences and technology Functionalized silicone rubber IRRADIATION Machinery and processing MATERIALS SCIENCE national synchrotron light source OZONE Plastics Polymer industry, paints, wood Self-assembly SILANES SILICONES Surface modification SURFACES Technology of polymers ULTRAVIOLET RADIATION |
title | Rapid formation of soft hydrophilic silicone elastomer surfaces |
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