Soluble ethane-bridged silsesquioxane polymer by hydrolysis–condensation of bis(trimethoxysilyl)ethane: characterization and mixing in organic polymers
Gel structure of ethane-bridged trialkoxysilsesquioxane has been investigated extensively. In contrast, only a few studies have focused on the characterization of soluble ethane-bridged silsesquioxane polymer (sEBSP) because of difficult preparation and isolation processes. The present study aims to...
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creator | Hayami, Ryohei Ideno, Yuzuko Sato, Yohei Tsukagoshi, Hayato Yamamoto, Kazuki Gunji, Takahiro |
description | Gel structure of ethane-bridged trialkoxysilsesquioxane has been investigated extensively. In contrast, only a few studies have focused on the characterization of soluble ethane-bridged silsesquioxane polymer (sEBSP) because of difficult preparation and isolation processes. The present study aims to characterize the sEBSP and investigate its mixing effect in an organic polymer. The sEBSP was prepared by the hydrolysis–condensation of bis(trimethoxysilyl)ethane under a nitrogen flow and characterized by nuclear magnetic resonance spectroscopy (NMR), Fourier-transform infrared (FTIR) spectroscopy, and gel permeation chromatography (GPC). Based on the NMR and FTIR results, sEBSP was characterized as a randomly structured polymer with hybridized linear, cyclic, branched, and bicyclic units. It was mixed with poly(methyl methacrylate) (PMMA) and poly(bisphenol A-
co
-epichlorohydrin) (PBE) to form PMMA–sEBSP and PBE–sEBSP, respectively, which were then characterized by FTIR spectroscopy. The results confirmed the formation of hydrogen bonds between sEBSP and the organic polymer. The thermal stabilities of PMMA–sEBSP were better than those of the pure polymers. PBE–sEBSP exhibited a lower 5% weight loss temperature (
T
d5
) because of the transalkoxylation between PBE and sEBSP. The miscibility of organic polymers and sEBSP was confirmed by differential scanning calorimetry (DSC). Based on their glass transition temperature, PMMA–sEBSP and PBE–sEBSP were classified as a hybrid and nanocomposite, respectively. Therefore, sEBSP was miscible to PMMA and PBE and affected to thermal properties. |
doi_str_mv | 10.1007/s10965-020-02294-z |
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co
-epichlorohydrin) (PBE) to form PMMA–sEBSP and PBE–sEBSP, respectively, which were then characterized by FTIR spectroscopy. The results confirmed the formation of hydrogen bonds between sEBSP and the organic polymer. The thermal stabilities of PMMA–sEBSP were better than those of the pure polymers. PBE–sEBSP exhibited a lower 5% weight loss temperature (
T
d5
) because of the transalkoxylation between PBE and sEBSP. The miscibility of organic polymers and sEBSP was confirmed by differential scanning calorimetry (DSC). Based on their glass transition temperature, PMMA–sEBSP and PBE–sEBSP were classified as a hybrid and nanocomposite, respectively. Therefore, sEBSP was miscible to PMMA and PBE and affected to thermal properties.</description><identifier>ISSN: 1022-9760</identifier><identifier>EISSN: 1572-8935</identifier><identifier>DOI: 10.1007/s10965-020-02294-z</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Bisphenol A ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Condensation polymerization ; Epichlorohydrin ; Ethane ; Fourier transforms ; Glass transition temperature ; Hydrogen bonds ; Hydrolysis ; Industrial Chemistry/Chemical Engineering ; Infrared spectroscopy ; Liquid chromatography ; Miscibility ; Nanocomposites ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Original Paper ; Polymer Sciences ; Polymers ; Polymethyl methacrylate ; Spectrum analysis ; Thermodynamic properties ; Weight loss</subject><ispartof>Journal of polymer research, 2020, Vol.27 (10), Article 316</ispartof><rights>The Polymer Society, Taipei 2020</rights><rights>The Polymer Society, Taipei 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-747a44d033d598b5d145d0241729e0c8a292acf56ee8084ddb3a37399a08f0c23</citedby><cites>FETCH-LOGICAL-c356t-747a44d033d598b5d145d0241729e0c8a292acf56ee8084ddb3a37399a08f0c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10965-020-02294-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10965-020-02294-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Hayami, Ryohei</creatorcontrib><creatorcontrib>Ideno, Yuzuko</creatorcontrib><creatorcontrib>Sato, Yohei</creatorcontrib><creatorcontrib>Tsukagoshi, Hayato</creatorcontrib><creatorcontrib>Yamamoto, Kazuki</creatorcontrib><creatorcontrib>Gunji, Takahiro</creatorcontrib><title>Soluble ethane-bridged silsesquioxane polymer by hydrolysis–condensation of bis(trimethoxysilyl)ethane: characterization and mixing in organic polymers</title><title>Journal of polymer research</title><addtitle>J Polym Res</addtitle><description>Gel structure of ethane-bridged trialkoxysilsesquioxane has been investigated extensively. In contrast, only a few studies have focused on the characterization of soluble ethane-bridged silsesquioxane polymer (sEBSP) because of difficult preparation and isolation processes. The present study aims to characterize the sEBSP and investigate its mixing effect in an organic polymer. The sEBSP was prepared by the hydrolysis–condensation of bis(trimethoxysilyl)ethane under a nitrogen flow and characterized by nuclear magnetic resonance spectroscopy (NMR), Fourier-transform infrared (FTIR) spectroscopy, and gel permeation chromatography (GPC). Based on the NMR and FTIR results, sEBSP was characterized as a randomly structured polymer with hybridized linear, cyclic, branched, and bicyclic units. It was mixed with poly(methyl methacrylate) (PMMA) and poly(bisphenol A-
co
-epichlorohydrin) (PBE) to form PMMA–sEBSP and PBE–sEBSP, respectively, which were then characterized by FTIR spectroscopy. The results confirmed the formation of hydrogen bonds between sEBSP and the organic polymer. The thermal stabilities of PMMA–sEBSP were better than those of the pure polymers. PBE–sEBSP exhibited a lower 5% weight loss temperature (
T
d5
) because of the transalkoxylation between PBE and sEBSP. The miscibility of organic polymers and sEBSP was confirmed by differential scanning calorimetry (DSC). Based on their glass transition temperature, PMMA–sEBSP and PBE–sEBSP were classified as a hybrid and nanocomposite, respectively. Therefore, sEBSP was miscible to PMMA and PBE and affected to thermal properties.</description><subject>Bisphenol A</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Condensation polymerization</subject><subject>Epichlorohydrin</subject><subject>Ethane</subject><subject>Fourier transforms</subject><subject>Glass transition temperature</subject><subject>Hydrogen bonds</subject><subject>Hydrolysis</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Infrared spectroscopy</subject><subject>Liquid chromatography</subject><subject>Miscibility</subject><subject>Nanocomposites</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Original Paper</subject><subject>Polymer Sciences</subject><subject>Polymers</subject><subject>Polymethyl methacrylate</subject><subject>Spectrum analysis</subject><subject>Thermodynamic properties</subject><subject>Weight loss</subject><issn>1022-9760</issn><issn>1572-8935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kc1OxCAUhRujiTr6Aq5I3OiiegulFHfG-JeYuFDXhAKdwXRghE4ynZXv4MrX80lEq3HngsC9-c65l5wsOyjgpABgp7EAXtEcMKSDeZmvN7KdgjKc15zQzfRO7ZyzCraz3RifAShlVb2TvT_4btl0Bpl-Jp3Jm2D11GgUbRdNfFlav0pttPDdMDcBNQOaDTqkKtr48fqmvNPGRdlb75BvUWPjUR_sPLn5VWK6oTsenc-QmskgVW-CXY-8dBrN7cq6KbJJHabSWfU7Ku5lW61MS-z_3JPs6ery8eImv7u_vr04v8sVoVWfs5LJstRAiKa8bqguSqoBlwXD3ICqJeZYqpZWxtRQl1o3RBJGOJdQt6AwmWSHo-8i-Jelib149svg0kiBSwqYclaQROGRUsHHGEwrFumbMgyiAPEVgRgjECkC8R2BWCcRGUUxwW5qwp_1P6pPOFeP2w</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Hayami, Ryohei</creator><creator>Ideno, Yuzuko</creator><creator>Sato, Yohei</creator><creator>Tsukagoshi, Hayato</creator><creator>Yamamoto, Kazuki</creator><creator>Gunji, Takahiro</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>2020</creationdate><title>Soluble ethane-bridged silsesquioxane polymer by hydrolysis–condensation of bis(trimethoxysilyl)ethane: characterization and mixing in organic polymers</title><author>Hayami, Ryohei ; Ideno, Yuzuko ; Sato, Yohei ; Tsukagoshi, Hayato ; Yamamoto, Kazuki ; Gunji, Takahiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-747a44d033d598b5d145d0241729e0c8a292acf56ee8084ddb3a37399a08f0c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bisphenol A</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Condensation polymerization</topic><topic>Epichlorohydrin</topic><topic>Ethane</topic><topic>Fourier transforms</topic><topic>Glass transition temperature</topic><topic>Hydrogen bonds</topic><topic>Hydrolysis</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Infrared spectroscopy</topic><topic>Liquid chromatography</topic><topic>Miscibility</topic><topic>Nanocomposites</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Original Paper</topic><topic>Polymer Sciences</topic><topic>Polymers</topic><topic>Polymethyl methacrylate</topic><topic>Spectrum analysis</topic><topic>Thermodynamic properties</topic><topic>Weight loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hayami, Ryohei</creatorcontrib><creatorcontrib>Ideno, Yuzuko</creatorcontrib><creatorcontrib>Sato, Yohei</creatorcontrib><creatorcontrib>Tsukagoshi, Hayato</creatorcontrib><creatorcontrib>Yamamoto, Kazuki</creatorcontrib><creatorcontrib>Gunji, Takahiro</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of polymer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hayami, Ryohei</au><au>Ideno, Yuzuko</au><au>Sato, Yohei</au><au>Tsukagoshi, Hayato</au><au>Yamamoto, Kazuki</au><au>Gunji, Takahiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soluble ethane-bridged silsesquioxane polymer by hydrolysis–condensation of bis(trimethoxysilyl)ethane: characterization and mixing in organic polymers</atitle><jtitle>Journal of polymer research</jtitle><stitle>J Polym Res</stitle><date>2020</date><risdate>2020</risdate><volume>27</volume><issue>10</issue><artnum>316</artnum><issn>1022-9760</issn><eissn>1572-8935</eissn><abstract>Gel structure of ethane-bridged trialkoxysilsesquioxane has been investigated extensively. In contrast, only a few studies have focused on the characterization of soluble ethane-bridged silsesquioxane polymer (sEBSP) because of difficult preparation and isolation processes. The present study aims to characterize the sEBSP and investigate its mixing effect in an organic polymer. The sEBSP was prepared by the hydrolysis–condensation of bis(trimethoxysilyl)ethane under a nitrogen flow and characterized by nuclear magnetic resonance spectroscopy (NMR), Fourier-transform infrared (FTIR) spectroscopy, and gel permeation chromatography (GPC). Based on the NMR and FTIR results, sEBSP was characterized as a randomly structured polymer with hybridized linear, cyclic, branched, and bicyclic units. It was mixed with poly(methyl methacrylate) (PMMA) and poly(bisphenol A-
co
-epichlorohydrin) (PBE) to form PMMA–sEBSP and PBE–sEBSP, respectively, which were then characterized by FTIR spectroscopy. The results confirmed the formation of hydrogen bonds between sEBSP and the organic polymer. The thermal stabilities of PMMA–sEBSP were better than those of the pure polymers. PBE–sEBSP exhibited a lower 5% weight loss temperature (
T
d5
) because of the transalkoxylation between PBE and sEBSP. The miscibility of organic polymers and sEBSP was confirmed by differential scanning calorimetry (DSC). Based on their glass transition temperature, PMMA–sEBSP and PBE–sEBSP were classified as a hybrid and nanocomposite, respectively. Therefore, sEBSP was miscible to PMMA and PBE and affected to thermal properties.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10965-020-02294-z</doi></addata></record> |
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subjects | Bisphenol A Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Condensation polymerization Epichlorohydrin Ethane Fourier transforms Glass transition temperature Hydrogen bonds Hydrolysis Industrial Chemistry/Chemical Engineering Infrared spectroscopy Liquid chromatography Miscibility Nanocomposites NMR NMR spectroscopy Nuclear magnetic resonance Original Paper Polymer Sciences Polymers Polymethyl methacrylate Spectrum analysis Thermodynamic properties Weight loss |
title | Soluble ethane-bridged silsesquioxane polymer by hydrolysis–condensation of bis(trimethoxysilyl)ethane: characterization and mixing in organic polymers |
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