Polyhydroxylated Nanosized Graphite as Multifunctional Building Block for Polyurethanes
Polyurethane nanocomposites were prepared with a nanosized high surface area graphite (HSAG) functionalized on its edges with hydroxyl groups as a building block. Edge functionalization of HSAG was obtained through reaction with KOH. The addition of OH groups was demonstrated by means of infrared (F...
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creator | Rubino, Lucia Torrisi, Giulio Brambilla, Luigi Rubino, Luca Ortenzi, Marco Aldo Galimberti, Maurizio Barbera, Vincenzina |
description | Polyurethane nanocomposites were prepared with a nanosized high surface area graphite (HSAG) functionalized on its edges with hydroxyl groups as a building block. Edge functionalization of HSAG was obtained through reaction with KOH. The addition of OH groups was demonstrated by means of infrared (FTIR) and thermogravimetric analysis (TGA), and the Boehm titration allowed estimation of a level of about 5.0 mmol
/g
. Results from wide-angle X-ray diffraction (WAXD) and Raman spectroscopy suggested that functionalization of the graphene layers occurred on the edges. The evaluation of the Hansen solubility parameters of G-OH revealed a substantial increase of
and
parameters with respect to HSAG. In line with these findings, homogeneous and stable dispersions of G-OH in a polyol were obtained. PU were prepared by mixing a dispersion of G-OH in
-1,4-butenediol with hexamethylene diisocyanate. A model reaction between catechol, 1,4-butanediol, and hexamethylene diisocyanate demonstrated the reactivity of hydroxylated aromatic rings with isocyanate groups. PU-based G-OH, characterized with WAXD and differential scanning calorimetry (DSC), revealed lower T
, higher T
, T
, and crystallinity than PU without G-OH. These results could be due to the higher flexibility of the polymer chains, likely a consequence of the dilution of the urethane bonds by the carbon substrate. Hence, G-OH allowed the preparation of PU with a larger temperature range between T
and T
, with potential positive impact on material applications. The model reaction between butylisocyanate and 1-butanol revealed that HSAG and G-OH promote efficient formation of the urethane bond, even in the absence of a catalyst. The effect of high surface area carbon on the nucleophilic oxygen attack to the isocyanate group can be hypothesized. The results here reported lead us to comment that a reactive nanosized sp
carbon allotrope, such as G-OH, can be used as a multifunctional building block of PU. Indeed, G-OH is a comonomer of PU, a promoter of the polymerization reaction, and can definitely act as reinforcing filler by tuning its amount in the final nanocomposite leading to highly versatile materials. The larger temperature range between T
and T
, together with the presence of G-OH acting as a reinforcing agent, could allow the production of piezoresistive sensing, shape-memory PU with good mechanical features. |
doi_str_mv | 10.3390/polym14061159 |
format | Article |
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/g
. Results from wide-angle X-ray diffraction (WAXD) and Raman spectroscopy suggested that functionalization of the graphene layers occurred on the edges. The evaluation of the Hansen solubility parameters of G-OH revealed a substantial increase of
and
parameters with respect to HSAG. In line with these findings, homogeneous and stable dispersions of G-OH in a polyol were obtained. PU were prepared by mixing a dispersion of G-OH in
-1,4-butenediol with hexamethylene diisocyanate. A model reaction between catechol, 1,4-butanediol, and hexamethylene diisocyanate demonstrated the reactivity of hydroxylated aromatic rings with isocyanate groups. PU-based G-OH, characterized with WAXD and differential scanning calorimetry (DSC), revealed lower T
, higher T
, T
, and crystallinity than PU without G-OH. These results could be due to the higher flexibility of the polymer chains, likely a consequence of the dilution of the urethane bonds by the carbon substrate. Hence, G-OH allowed the preparation of PU with a larger temperature range between T
and T
, with potential positive impact on material applications. The model reaction between butylisocyanate and 1-butanol revealed that HSAG and G-OH promote efficient formation of the urethane bond, even in the absence of a catalyst. The effect of high surface area carbon on the nucleophilic oxygen attack to the isocyanate group can be hypothesized. The results here reported lead us to comment that a reactive nanosized sp
carbon allotrope, such as G-OH, can be used as a multifunctional building block of PU. Indeed, G-OH is a comonomer of PU, a promoter of the polymerization reaction, and can definitely act as reinforcing filler by tuning its amount in the final nanocomposite leading to highly versatile materials. The larger temperature range between T
and T
, together with the presence of G-OH acting as a reinforcing agent, could allow the production of piezoresistive sensing, shape-memory PU with good mechanical features.</description><identifier>ISSN: 2073-4360</identifier><identifier>EISSN: 2073-4360</identifier><identifier>DOI: 10.3390/polym14061159</identifier><identifier>PMID: 35335490</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Allotropy ; Aromatic compounds ; Butanediol ; Butanol ; Carbon ; Catechol ; Dilution ; Fourier transforms ; Graphene ; Graphite ; Hexamethylene diisocyanate ; Hydroxyl groups ; Infrared analysis ; Isocyanates ; Mathematical models ; Nanocomposites ; Nanoparticles ; Polymerization ; Polymers ; Polyurethane ; Polyurethane resins ; Raman spectroscopy ; Reagents ; Shape memory ; Solubility parameters ; Spectrum analysis ; Substrates ; Surface area ; Thermogravimetric analysis ; Titration</subject><ispartof>Polymers, 2022-03, Vol.14 (6), p.1159</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-c053ba0aa755fed317c207f9ed6454d547bf62c5e5a36e3b17a1089bfead2a133</citedby><cites>FETCH-LOGICAL-c415t-c053ba0aa755fed317c207f9ed6454d547bf62c5e5a36e3b17a1089bfead2a133</cites><orcidid>0000-0003-2264-1792 ; 0000-0001-6206-9589 ; 0000-0001-5770-7208 ; 0000-0002-4503-4250</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953097/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953097/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35335490$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rubino, Lucia</creatorcontrib><creatorcontrib>Torrisi, Giulio</creatorcontrib><creatorcontrib>Brambilla, Luigi</creatorcontrib><creatorcontrib>Rubino, Luca</creatorcontrib><creatorcontrib>Ortenzi, Marco Aldo</creatorcontrib><creatorcontrib>Galimberti, Maurizio</creatorcontrib><creatorcontrib>Barbera, Vincenzina</creatorcontrib><title>Polyhydroxylated Nanosized Graphite as Multifunctional Building Block for Polyurethanes</title><title>Polymers</title><addtitle>Polymers (Basel)</addtitle><description>Polyurethane nanocomposites were prepared with a nanosized high surface area graphite (HSAG) functionalized on its edges with hydroxyl groups as a building block. Edge functionalization of HSAG was obtained through reaction with KOH. The addition of OH groups was demonstrated by means of infrared (FTIR) and thermogravimetric analysis (TGA), and the Boehm titration allowed estimation of a level of about 5.0 mmol
/g
. Results from wide-angle X-ray diffraction (WAXD) and Raman spectroscopy suggested that functionalization of the graphene layers occurred on the edges. The evaluation of the Hansen solubility parameters of G-OH revealed a substantial increase of
and
parameters with respect to HSAG. In line with these findings, homogeneous and stable dispersions of G-OH in a polyol were obtained. PU were prepared by mixing a dispersion of G-OH in
-1,4-butenediol with hexamethylene diisocyanate. A model reaction between catechol, 1,4-butanediol, and hexamethylene diisocyanate demonstrated the reactivity of hydroxylated aromatic rings with isocyanate groups. PU-based G-OH, characterized with WAXD and differential scanning calorimetry (DSC), revealed lower T
, higher T
, T
, and crystallinity than PU without G-OH. These results could be due to the higher flexibility of the polymer chains, likely a consequence of the dilution of the urethane bonds by the carbon substrate. Hence, G-OH allowed the preparation of PU with a larger temperature range between T
and T
, with potential positive impact on material applications. The model reaction between butylisocyanate and 1-butanol revealed that HSAG and G-OH promote efficient formation of the urethane bond, even in the absence of a catalyst. The effect of high surface area carbon on the nucleophilic oxygen attack to the isocyanate group can be hypothesized. The results here reported lead us to comment that a reactive nanosized sp
carbon allotrope, such as G-OH, can be used as a multifunctional building block of PU. Indeed, G-OH is a comonomer of PU, a promoter of the polymerization reaction, and can definitely act as reinforcing filler by tuning its amount in the final nanocomposite leading to highly versatile materials. The larger temperature range between T
and T
, together with the presence of G-OH acting as a reinforcing agent, could allow the production of piezoresistive sensing, shape-memory PU with good mechanical features.</description><subject>Allotropy</subject><subject>Aromatic compounds</subject><subject>Butanediol</subject><subject>Butanol</subject><subject>Carbon</subject><subject>Catechol</subject><subject>Dilution</subject><subject>Fourier transforms</subject><subject>Graphene</subject><subject>Graphite</subject><subject>Hexamethylene diisocyanate</subject><subject>Hydroxyl groups</subject><subject>Infrared analysis</subject><subject>Isocyanates</subject><subject>Mathematical models</subject><subject>Nanocomposites</subject><subject>Nanoparticles</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Polyurethane</subject><subject>Polyurethane resins</subject><subject>Raman spectroscopy</subject><subject>Reagents</subject><subject>Shape memory</subject><subject>Solubility parameters</subject><subject>Spectrum analysis</subject><subject>Substrates</subject><subject>Surface area</subject><subject>Thermogravimetric analysis</subject><subject>Titration</subject><issn>2073-4360</issn><issn>2073-4360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkctLxDAQh4Mouqx79CoFL16qSfPo9iLo4gt8HRSPYZqmbtZssyatWP96o6uyOpcZyMfHTH4I7RB8QGmBDxfO9nPCsCCEF2tokOGcpowKvL4yb6FRCDMci3EhSL6JtiinlLMCD9DjXVRM-8q7t95Cq6vkBhoXzHuczj0spqbVCYTkurOtqbtGtcY1YJOTztjKNE_JiXXqOamdTz5NndftFBodttFGDTbo0Xcfooez0_vJRXp1e345Ob5KFSO8TRXmtAQMkHNe64qSXMW960JXgnFWcZaXtcgU1xyo0LQkORA8LspaQ5UBoXSIjpbeRVfOdaV003qwcuHNHHwvHRj596UxU_nkXuW44BQXeRTsfwu8e-l0aOXcBKWtjVe4LshMMIYxEZREdO8fOnOdj7_xRWVMZBnGkUqXlPIuBK_r32UIlp-pyT-pRX539YJf-icj-gG4cpWX</recordid><startdate>20220314</startdate><enddate>20220314</enddate><creator>Rubino, Lucia</creator><creator>Torrisi, Giulio</creator><creator>Brambilla, Luigi</creator><creator>Rubino, Luca</creator><creator>Ortenzi, Marco Aldo</creator><creator>Galimberti, Maurizio</creator><creator>Barbera, Vincenzina</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2264-1792</orcidid><orcidid>https://orcid.org/0000-0001-6206-9589</orcidid><orcidid>https://orcid.org/0000-0001-5770-7208</orcidid><orcidid>https://orcid.org/0000-0002-4503-4250</orcidid></search><sort><creationdate>20220314</creationdate><title>Polyhydroxylated Nanosized Graphite as Multifunctional Building Block for Polyurethanes</title><author>Rubino, Lucia ; Torrisi, Giulio ; Brambilla, Luigi ; Rubino, Luca ; Ortenzi, Marco Aldo ; Galimberti, Maurizio ; Barbera, Vincenzina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-c053ba0aa755fed317c207f9ed6454d547bf62c5e5a36e3b17a1089bfead2a133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Allotropy</topic><topic>Aromatic compounds</topic><topic>Butanediol</topic><topic>Butanol</topic><topic>Carbon</topic><topic>Catechol</topic><topic>Dilution</topic><topic>Fourier transforms</topic><topic>Graphene</topic><topic>Graphite</topic><topic>Hexamethylene diisocyanate</topic><topic>Hydroxyl groups</topic><topic>Infrared analysis</topic><topic>Isocyanates</topic><topic>Mathematical models</topic><topic>Nanocomposites</topic><topic>Nanoparticles</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Polyurethane</topic><topic>Polyurethane resins</topic><topic>Raman spectroscopy</topic><topic>Reagents</topic><topic>Shape memory</topic><topic>Solubility parameters</topic><topic>Spectrum analysis</topic><topic>Substrates</topic><topic>Surface area</topic><topic>Thermogravimetric analysis</topic><topic>Titration</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rubino, Lucia</creatorcontrib><creatorcontrib>Torrisi, Giulio</creatorcontrib><creatorcontrib>Brambilla, Luigi</creatorcontrib><creatorcontrib>Rubino, Luca</creatorcontrib><creatorcontrib>Ortenzi, Marco Aldo</creatorcontrib><creatorcontrib>Galimberti, Maurizio</creatorcontrib><creatorcontrib>Barbera, Vincenzina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rubino, Lucia</au><au>Torrisi, Giulio</au><au>Brambilla, Luigi</au><au>Rubino, Luca</au><au>Ortenzi, Marco Aldo</au><au>Galimberti, Maurizio</au><au>Barbera, Vincenzina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyhydroxylated Nanosized Graphite as Multifunctional Building Block for Polyurethanes</atitle><jtitle>Polymers</jtitle><addtitle>Polymers (Basel)</addtitle><date>2022-03-14</date><risdate>2022</risdate><volume>14</volume><issue>6</issue><spage>1159</spage><pages>1159-</pages><issn>2073-4360</issn><eissn>2073-4360</eissn><abstract>Polyurethane nanocomposites were prepared with a nanosized high surface area graphite (HSAG) functionalized on its edges with hydroxyl groups as a building block. Edge functionalization of HSAG was obtained through reaction with KOH. The addition of OH groups was demonstrated by means of infrared (FTIR) and thermogravimetric analysis (TGA), and the Boehm titration allowed estimation of a level of about 5.0 mmol
/g
. Results from wide-angle X-ray diffraction (WAXD) and Raman spectroscopy suggested that functionalization of the graphene layers occurred on the edges. The evaluation of the Hansen solubility parameters of G-OH revealed a substantial increase of
and
parameters with respect to HSAG. In line with these findings, homogeneous and stable dispersions of G-OH in a polyol were obtained. PU were prepared by mixing a dispersion of G-OH in
-1,4-butenediol with hexamethylene diisocyanate. A model reaction between catechol, 1,4-butanediol, and hexamethylene diisocyanate demonstrated the reactivity of hydroxylated aromatic rings with isocyanate groups. PU-based G-OH, characterized with WAXD and differential scanning calorimetry (DSC), revealed lower T
, higher T
, T
, and crystallinity than PU without G-OH. These results could be due to the higher flexibility of the polymer chains, likely a consequence of the dilution of the urethane bonds by the carbon substrate. Hence, G-OH allowed the preparation of PU with a larger temperature range between T
and T
, with potential positive impact on material applications. The model reaction between butylisocyanate and 1-butanol revealed that HSAG and G-OH promote efficient formation of the urethane bond, even in the absence of a catalyst. The effect of high surface area carbon on the nucleophilic oxygen attack to the isocyanate group can be hypothesized. The results here reported lead us to comment that a reactive nanosized sp
carbon allotrope, such as G-OH, can be used as a multifunctional building block of PU. Indeed, G-OH is a comonomer of PU, a promoter of the polymerization reaction, and can definitely act as reinforcing filler by tuning its amount in the final nanocomposite leading to highly versatile materials. The larger temperature range between T
and T
, together with the presence of G-OH acting as a reinforcing agent, could allow the production of piezoresistive sensing, shape-memory PU with good mechanical features.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35335490</pmid><doi>10.3390/polym14061159</doi><orcidid>https://orcid.org/0000-0003-2264-1792</orcidid><orcidid>https://orcid.org/0000-0001-6206-9589</orcidid><orcidid>https://orcid.org/0000-0001-5770-7208</orcidid><orcidid>https://orcid.org/0000-0002-4503-4250</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Allotropy Aromatic compounds Butanediol Butanol Carbon Catechol Dilution Fourier transforms Graphene Graphite Hexamethylene diisocyanate Hydroxyl groups Infrared analysis Isocyanates Mathematical models Nanocomposites Nanoparticles Polymerization Polymers Polyurethane Polyurethane resins Raman spectroscopy Reagents Shape memory Solubility parameters Spectrum analysis Substrates Surface area Thermogravimetric analysis Titration |
title | Polyhydroxylated Nanosized Graphite as Multifunctional Building Block for Polyurethanes |
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