Composites of Kaolin and Polydimethylsiloxane
Kaolin particles were surface-treated with isobutyltrimethoxysilane (IBTMS), hydrogenated tallow (HT), and a polyisobutyl chain-based stabilizer (SAP) to make composites with polydimethylsiloxane (PDMS). IBTMS did not cover the strong acid sites on the kaolin surface and as a result a cross-linking...
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Veröffentlicht in: | Langmuir 2008-10, Vol.24 (20), p.12032-12039 |
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creator | Zhang, Yan Gittins, David I Skuse, David Cosgrove, Terence van Duijneveldt, Jeroen S |
description | Kaolin particles were surface-treated with isobutyltrimethoxysilane (IBTMS), hydrogenated tallow (HT), and a polyisobutyl chain-based stabilizer (SAP) to make composites with polydimethylsiloxane (PDMS). IBTMS did not cover the strong acid sites on the kaolin surface and as a result a cross-linking reaction occurred for silanol-terminated PDMS. The polyisobutyl chain of SAP was found to be incompatible with PDMS and this caused aggregation of the kaolin particles. HT was the most effective at dispersing the particles into silanol-terminated PDMS. The aggregation state of the composites was characterized using rheology and microscopy. Both showed the HT-treated particles were well-dispersed in low molecular weight silanol-terminated PDMS, and they were weakly flocculated in higher molecular weight silanol-terminated PDMS. However, the same particles aggregated when dispersed in methyl-terminated PDMS. It appears the silanol-terminated PDMS acted as costabilizer through interaction with the kaolin surface. Transverse relaxation NMR was used to probe mobility of the PDMS chains in the composites. This showed little dependence on surface treatment, aggregation state, or polymer end groups. For all samples, chain mobility decreased with increasing kaolin concentration. |
doi_str_mv | 10.1021/la8018259 |
format | Article |
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IBTMS did not cover the strong acid sites on the kaolin surface and as a result a cross-linking reaction occurred for silanol-terminated PDMS. The polyisobutyl chain of SAP was found to be incompatible with PDMS and this caused aggregation of the kaolin particles. HT was the most effective at dispersing the particles into silanol-terminated PDMS. The aggregation state of the composites was characterized using rheology and microscopy. Both showed the HT-treated particles were well-dispersed in low molecular weight silanol-terminated PDMS, and they were weakly flocculated in higher molecular weight silanol-terminated PDMS. However, the same particles aggregated when dispersed in methyl-terminated PDMS. It appears the silanol-terminated PDMS acted as costabilizer through interaction with the kaolin surface. Transverse relaxation NMR was used to probe mobility of the PDMS chains in the composites. This showed little dependence on surface treatment, aggregation state, or polymer end groups. For all samples, chain mobility decreased with increasing kaolin concentration.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la8018259</identifier><identifier>PMID: 18823089</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; General and physical chemistry ; Materials: Nano-and Mesostructured Materials, Polymers, Gels, Liquid Crystals, Composites ; Surface physical chemistry</subject><ispartof>Langmuir, 2008-10, Vol.24 (20), p.12032-12039</ispartof><rights>Copyright © 2008 American Chemical Society</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-f7638e79cabc85e355241198db4f76bec1e684a5235e1f0c6af3dc1dc5b68653</citedby><cites>FETCH-LOGICAL-a381t-f7638e79cabc85e355241198db4f76bec1e684a5235e1f0c6af3dc1dc5b68653</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/la8018259$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la8018259$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20768506$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18823089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Gittins, David I</creatorcontrib><creatorcontrib>Skuse, David</creatorcontrib><creatorcontrib>Cosgrove, Terence</creatorcontrib><creatorcontrib>van Duijneveldt, Jeroen S</creatorcontrib><title>Composites of Kaolin and Polydimethylsiloxane</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Kaolin particles were surface-treated with isobutyltrimethoxysilane (IBTMS), hydrogenated tallow (HT), and a polyisobutyl chain-based stabilizer (SAP) to make composites with polydimethylsiloxane (PDMS). IBTMS did not cover the strong acid sites on the kaolin surface and as a result a cross-linking reaction occurred for silanol-terminated PDMS. The polyisobutyl chain of SAP was found to be incompatible with PDMS and this caused aggregation of the kaolin particles. HT was the most effective at dispersing the particles into silanol-terminated PDMS. The aggregation state of the composites was characterized using rheology and microscopy. Both showed the HT-treated particles were well-dispersed in low molecular weight silanol-terminated PDMS, and they were weakly flocculated in higher molecular weight silanol-terminated PDMS. However, the same particles aggregated when dispersed in methyl-terminated PDMS. It appears the silanol-terminated PDMS acted as costabilizer through interaction with the kaolin surface. Transverse relaxation NMR was used to probe mobility of the PDMS chains in the composites. This showed little dependence on surface treatment, aggregation state, or polymer end groups. For all samples, chain mobility decreased with increasing kaolin concentration.</description><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Materials: Nano-and Mesostructured Materials, Polymers, Gels, Liquid Crystals, Composites</subject><subject>Surface physical chemistry</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNpt0E9LwzAYBvAgipvTg19AelHwUE2aJk2OOv_i0MF6D2maYmbazKSF7dvbsTI9eHoP74-HhweAcwRvEEzQrZUMIpYQfgDGiCQwJizJDsEYZimOs5TiETgJYQkh5Djlx2CEGEswZHwM4qmrVy6YVofIVdGbdNY0kWzKaO7spjS1bj83Nhjr1rLRp-Cokjbos-FOQP70mE9f4tnH8-v0bhZLzFAbVxnFTGdcyUIxojEhSYoQZ2WR9q9CK6QpSyVJMNGogorKCpcKlYoUlFGCJ-BqF7vy7rvToRW1CUpb21dwXRCUUwrTdAuvd1B5F4LXlVh5U0u_EQiK7TRiP01vL4bQrqh1-SuHLXpwOQAZlLSVl40yYe8SmFFGIO1dvHMmtHq9_0v_JWiGMyLy-ULQ9_zhfoG4-JMrVRBL1_mmn-6fgj8BeoUY</recordid><startdate>20081021</startdate><enddate>20081021</enddate><creator>Zhang, Yan</creator><creator>Gittins, David I</creator><creator>Skuse, David</creator><creator>Cosgrove, Terence</creator><creator>van Duijneveldt, Jeroen S</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20081021</creationdate><title>Composites of Kaolin and Polydimethylsiloxane</title><author>Zhang, Yan ; Gittins, David I ; Skuse, David ; Cosgrove, Terence ; van Duijneveldt, Jeroen S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-f7638e79cabc85e355241198db4f76bec1e684a5235e1f0c6af3dc1dc5b68653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Materials: Nano-and Mesostructured Materials, Polymers, Gels, Liquid Crystals, Composites</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Gittins, David I</creatorcontrib><creatorcontrib>Skuse, David</creatorcontrib><creatorcontrib>Cosgrove, Terence</creatorcontrib><creatorcontrib>van Duijneveldt, Jeroen S</creatorcontrib><collection>Istex</collection><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>Zhang, Yan</au><au>Gittins, David I</au><au>Skuse, David</au><au>Cosgrove, Terence</au><au>van Duijneveldt, Jeroen S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Composites of Kaolin and Polydimethylsiloxane</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2008-10-21</date><risdate>2008</risdate><volume>24</volume><issue>20</issue><spage>12032</spage><epage>12039</epage><pages>12032-12039</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>Kaolin particles were surface-treated with isobutyltrimethoxysilane (IBTMS), hydrogenated tallow (HT), and a polyisobutyl chain-based stabilizer (SAP) to make composites with polydimethylsiloxane (PDMS). IBTMS did not cover the strong acid sites on the kaolin surface and as a result a cross-linking reaction occurred for silanol-terminated PDMS. The polyisobutyl chain of SAP was found to be incompatible with PDMS and this caused aggregation of the kaolin particles. HT was the most effective at dispersing the particles into silanol-terminated PDMS. The aggregation state of the composites was characterized using rheology and microscopy. Both showed the HT-treated particles were well-dispersed in low molecular weight silanol-terminated PDMS, and they were weakly flocculated in higher molecular weight silanol-terminated PDMS. However, the same particles aggregated when dispersed in methyl-terminated PDMS. It appears the silanol-terminated PDMS acted as costabilizer through interaction with the kaolin surface. Transverse relaxation NMR was used to probe mobility of the PDMS chains in the composites. This showed little dependence on surface treatment, aggregation state, or polymer end groups. For all samples, chain mobility decreased with increasing kaolin concentration.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>18823089</pmid><doi>10.1021/la8018259</doi><tpages>8</tpages></addata></record> |
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subjects | Chemistry Colloidal state and disperse state Exact sciences and technology General and physical chemistry Materials: Nano-and Mesostructured Materials, Polymers, Gels, Liquid Crystals, Composites Surface physical chemistry |
title | Composites of Kaolin and Polydimethylsiloxane |
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