Synthesis and Characterization of a Poly(dimethylsiloxane)−Poly(ethylene oxide) Block Copolymer for Fabrication of Amphiphilic Surfaces on Microfluidic Devices
A poly(dimethylsiloxane)−poly(ethylene oxide) (PDMS−PEO) vinyl terminated block copolymer has been synthesized via a simple hydrosilylation reaction between hydride-terminated PDMS and PEO divinyl ether. This prepolymer can be subsequently cross-linked into an elastomer in a second hydrosilylation r...
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description | A poly(dimethylsiloxane)−poly(ethylene oxide) (PDMS−PEO) vinyl terminated block copolymer has been synthesized via a simple hydrosilylation reaction between hydride-terminated PDMS and PEO divinyl ether. This prepolymer can be subsequently cross-linked into an elastomer in a second hydrosilylation reaction involving a methylhydrosiloxane−dimethylsiloxane copolymer, forming a material suitable for the purposes of fabricating microfluidic devices. The presence of the PEO block in the prepolymer chain results in a much more hydrophilic material following cross-linking. The surface water contact angle of the PDMS−PEO material is 65° ± 3 (n = 6), as opposed to approximately 110° for native PDMS. Droplets of water straddled by air within molded channels of the PDMS−PEO are concave in shape with contact angles where the fluid meets the side walls of 32° ± 4 (n = 8), while droplets in PDMS microchannels are more convex with contact angles of 95° ± 6 (n = 6). The length of the PDMS−PEO prepolymer chain and the multifunctional hydride cross-linker chains appear to dictate the durability of the elastomeric material. Young’s modulus measurements yielded values of 0.94 ± 0.08, 2.6 ± 0.8, and 1.91 ± 0.06 MPa for a [5% vinyl excess prepolymer and 10-fold excess of cross-linker], [10% vinyl excess prepolymer and 5-fold excess of cross-linker], and 10:1 PDMS, respectively, confirming that the elasticity of the cross-linked PDMS−PEO is similar to that of PDMS (Sylgard 184:10:1 mixture of elastomeric base to elastomer curing agent). The PDMS−PEO material still possesses enough PDMS character to allow molded channel architectures to be sealed between two pieces of the block copolymer by conformal contact. As a result of the more hydrophilic nature of the material, the channels of devices fabricated from this polymer are self-filling when using aqueous buffers, making it more user-friendly than PDMS for applications calling for background electrolytes void of organic modifiers. Different compositions of PDMS−PEO devices feature different electroosmotic flow values with the 5% vinyl excess prepolymer EOF values of 2.5 ± 0.7 × 10−4 and 5.7 ± 0.8 × 10−4 cm2/(V s) at pHs 6 and 9, respectively, and 1.2 ± 0.3 × 10−4 and 2.5 ± 0.3 × 10−4 cm2/(V s) for the 10% vinyl excess prepolymer device at pHs 6 and 9, respectively. |
doi_str_mv | 10.1021/la900920q |
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This prepolymer can be subsequently cross-linked into an elastomer in a second hydrosilylation reaction involving a methylhydrosiloxane−dimethylsiloxane copolymer, forming a material suitable for the purposes of fabricating microfluidic devices. The presence of the PEO block in the prepolymer chain results in a much more hydrophilic material following cross-linking. The surface water contact angle of the PDMS−PEO material is 65° ± 3 (n = 6), as opposed to approximately 110° for native PDMS. Droplets of water straddled by air within molded channels of the PDMS−PEO are concave in shape with contact angles where the fluid meets the side walls of 32° ± 4 (n = 8), while droplets in PDMS microchannels are more convex with contact angles of 95° ± 6 (n = 6). The length of the PDMS−PEO prepolymer chain and the multifunctional hydride cross-linker chains appear to dictate the durability of the elastomeric material. Young’s modulus measurements yielded values of 0.94 ± 0.08, 2.6 ± 0.8, and 1.91 ± 0.06 MPa for a [5% vinyl excess prepolymer and 10-fold excess of cross-linker], [10% vinyl excess prepolymer and 5-fold excess of cross-linker], and 10:1 PDMS, respectively, confirming that the elasticity of the cross-linked PDMS−PEO is similar to that of PDMS (Sylgard 184:10:1 mixture of elastomeric base to elastomer curing agent). The PDMS−PEO material still possesses enough PDMS character to allow molded channel architectures to be sealed between two pieces of the block copolymer by conformal contact. As a result of the more hydrophilic nature of the material, the channels of devices fabricated from this polymer are self-filling when using aqueous buffers, making it more user-friendly than PDMS for applications calling for background electrolytes void of organic modifiers. Different compositions of PDMS−PEO devices feature different electroosmotic flow values with the 5% vinyl excess prepolymer EOF values of 2.5 ± 0.7 × 10−4 and 5.7 ± 0.8 × 10−4 cm2/(V s) at pHs 6 and 9, respectively, and 1.2 ± 0.3 × 10−4 and 2.5 ± 0.3 × 10−4 cm2/(V s) for the 10% vinyl excess prepolymer device at pHs 6 and 9, respectively.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la900920q</identifier><identifier>PMID: 19572528</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Chemistry ; Colloidal state and disperse state ; Devices and Applications: Sensors, Fluidics, Patterning, Catalysis, Photonic Crystals ; Exact sciences and technology ; General and physical chemistry ; Surface physical chemistry</subject><ispartof>Langmuir, 2009-09, Vol.25 (17), p.10390-10396</ispartof><rights>Copyright © 2009 American Chemical Society</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a343t-d4767de234c012deced441af75b995f8610cbf9175f79dbd6729bf9e20fffcc93</citedby><cites>FETCH-LOGICAL-a343t-d4767de234c012deced441af75b995f8610cbf9175f79dbd6729bf9e20fffcc93</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/la900920q$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la900920q$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2751,27055,27903,27904,56717,56767</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22069855$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19572528$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Klasner, Scott A</creatorcontrib><creatorcontrib>Metto, Eve C</creatorcontrib><creatorcontrib>Roman, Gregory T</creatorcontrib><creatorcontrib>Culbertson, Christopher T</creatorcontrib><title>Synthesis and Characterization of a Poly(dimethylsiloxane)−Poly(ethylene oxide) Block Copolymer for Fabrication of Amphiphilic Surfaces on Microfluidic Devices</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>A poly(dimethylsiloxane)−poly(ethylene oxide) (PDMS−PEO) vinyl terminated block copolymer has been synthesized via a simple hydrosilylation reaction between hydride-terminated PDMS and PEO divinyl ether. This prepolymer can be subsequently cross-linked into an elastomer in a second hydrosilylation reaction involving a methylhydrosiloxane−dimethylsiloxane copolymer, forming a material suitable for the purposes of fabricating microfluidic devices. The presence of the PEO block in the prepolymer chain results in a much more hydrophilic material following cross-linking. The surface water contact angle of the PDMS−PEO material is 65° ± 3 (n = 6), as opposed to approximately 110° for native PDMS. Droplets of water straddled by air within molded channels of the PDMS−PEO are concave in shape with contact angles where the fluid meets the side walls of 32° ± 4 (n = 8), while droplets in PDMS microchannels are more convex with contact angles of 95° ± 6 (n = 6). The length of the PDMS−PEO prepolymer chain and the multifunctional hydride cross-linker chains appear to dictate the durability of the elastomeric material. Young’s modulus measurements yielded values of 0.94 ± 0.08, 2.6 ± 0.8, and 1.91 ± 0.06 MPa for a [5% vinyl excess prepolymer and 10-fold excess of cross-linker], [10% vinyl excess prepolymer and 5-fold excess of cross-linker], and 10:1 PDMS, respectively, confirming that the elasticity of the cross-linked PDMS−PEO is similar to that of PDMS (Sylgard 184:10:1 mixture of elastomeric base to elastomer curing agent). The PDMS−PEO material still possesses enough PDMS character to allow molded channel architectures to be sealed between two pieces of the block copolymer by conformal contact. As a result of the more hydrophilic nature of the material, the channels of devices fabricated from this polymer are self-filling when using aqueous buffers, making it more user-friendly than PDMS for applications calling for background electrolytes void of organic modifiers. Different compositions of PDMS−PEO devices feature different electroosmotic flow values with the 5% vinyl excess prepolymer EOF values of 2.5 ± 0.7 × 10−4 and 5.7 ± 0.8 × 10−4 cm2/(V s) at pHs 6 and 9, respectively, and 1.2 ± 0.3 × 10−4 and 2.5 ± 0.3 × 10−4 cm2/(V s) for the 10% vinyl excess prepolymer device at pHs 6 and 9, respectively.</description><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Devices and Applications: Sensors, Fluidics, Patterning, Catalysis, Photonic Crystals</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Surface physical chemistry</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNptkcFO3DAQhq2qqGxpD7wA8qVV9xBqO3EcH2FbChKISrTnyLHHWlMnXuykYvsEPfMGvFqfBAOr5VLJ0sjzf_rHnh-hfUoOKWH0s1eSEMnIzSs0o5yRgjdMvEYzIqqyEFVd7qK3KV2TDJWVfIN2qeSCcdbM0P3VehiXkFzCajB4sVRR6RGi-6NGFwYcLFb4e_DrT8b1MC7XPjkfbtUA839_756Epy4MgMOtMzDHxz7oX3gRVlnsIWIbIj5RXXR6a3nUr5YuH-80vpqiVRoSztKF0zFYPzmThS_w2-X-O7RjlU_wflP30M-Trz8Wp8X55bezxdF5ocqqHAtTiVoYYGWlCWUGNJiqosoK3knJbVNTojsrqeBWSNOZWjCZ78CItVZrWe6hj8--qxhuJkhj27ukwfv81zClthY1aUoiMjh_BvNbU4pg21V0vYrrlpL2MY92m0dmDzamU9eDeSE3AWTgwwZQSStvoxq0S1uOMVLLhvMXTunUXocpDnkX_xn4AHm8o6U</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Klasner, Scott A</creator><creator>Metto, Eve C</creator><creator>Roman, Gregory T</creator><creator>Culbertson, Christopher T</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090901</creationdate><title>Synthesis and Characterization of a Poly(dimethylsiloxane)−Poly(ethylene oxide) Block Copolymer for Fabrication of Amphiphilic Surfaces on Microfluidic Devices</title><author>Klasner, Scott A ; Metto, Eve C ; Roman, Gregory T ; Culbertson, Christopher T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a343t-d4767de234c012deced441af75b995f8610cbf9175f79dbd6729bf9e20fffcc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Devices and Applications: Sensors, Fluidics, Patterning, Catalysis, Photonic Crystals</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Klasner, Scott A</creatorcontrib><creatorcontrib>Metto, Eve C</creatorcontrib><creatorcontrib>Roman, Gregory T</creatorcontrib><creatorcontrib>Culbertson, Christopher T</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Klasner, Scott A</au><au>Metto, Eve C</au><au>Roman, Gregory T</au><au>Culbertson, Christopher T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of a Poly(dimethylsiloxane)−Poly(ethylene oxide) Block Copolymer for Fabrication of Amphiphilic Surfaces on Microfluidic Devices</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>25</volume><issue>17</issue><spage>10390</spage><epage>10396</epage><pages>10390-10396</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>A poly(dimethylsiloxane)−poly(ethylene oxide) (PDMS−PEO) vinyl terminated block copolymer has been synthesized via a simple hydrosilylation reaction between hydride-terminated PDMS and PEO divinyl ether. This prepolymer can be subsequently cross-linked into an elastomer in a second hydrosilylation reaction involving a methylhydrosiloxane−dimethylsiloxane copolymer, forming a material suitable for the purposes of fabricating microfluidic devices. The presence of the PEO block in the prepolymer chain results in a much more hydrophilic material following cross-linking. The surface water contact angle of the PDMS−PEO material is 65° ± 3 (n = 6), as opposed to approximately 110° for native PDMS. Droplets of water straddled by air within molded channels of the PDMS−PEO are concave in shape with contact angles where the fluid meets the side walls of 32° ± 4 (n = 8), while droplets in PDMS microchannels are more convex with contact angles of 95° ± 6 (n = 6). The length of the PDMS−PEO prepolymer chain and the multifunctional hydride cross-linker chains appear to dictate the durability of the elastomeric material. Young’s modulus measurements yielded values of 0.94 ± 0.08, 2.6 ± 0.8, and 1.91 ± 0.06 MPa for a [5% vinyl excess prepolymer and 10-fold excess of cross-linker], [10% vinyl excess prepolymer and 5-fold excess of cross-linker], and 10:1 PDMS, respectively, confirming that the elasticity of the cross-linked PDMS−PEO is similar to that of PDMS (Sylgard 184:10:1 mixture of elastomeric base to elastomer curing agent). The PDMS−PEO material still possesses enough PDMS character to allow molded channel architectures to be sealed between two pieces of the block copolymer by conformal contact. As a result of the more hydrophilic nature of the material, the channels of devices fabricated from this polymer are self-filling when using aqueous buffers, making it more user-friendly than PDMS for applications calling for background electrolytes void of organic modifiers. Different compositions of PDMS−PEO devices feature different electroosmotic flow values with the 5% vinyl excess prepolymer EOF values of 2.5 ± 0.7 × 10−4 and 5.7 ± 0.8 × 10−4 cm2/(V s) at pHs 6 and 9, respectively, and 1.2 ± 0.3 × 10−4 and 2.5 ± 0.3 × 10−4 cm2/(V s) for the 10% vinyl excess prepolymer device at pHs 6 and 9, respectively.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>19572528</pmid><doi>10.1021/la900920q</doi><tpages>7</tpages></addata></record> |
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subjects | Chemistry Colloidal state and disperse state Devices and Applications: Sensors, Fluidics, Patterning, Catalysis, Photonic Crystals Exact sciences and technology General and physical chemistry Surface physical chemistry |
title | Synthesis and Characterization of a Poly(dimethylsiloxane)−Poly(ethylene oxide) Block Copolymer for Fabrication of Amphiphilic Surfaces on Microfluidic Devices |
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