Superstretchable, Self‐Healing Polymeric Elastomers with Tunable Properties
Utilization of self‐healing chemistry to develop synthetic polymer materials that can heal themselves with restored mechanical performance and functionality is of great interest. Self‐healable polymer elastomers with tunable mechanical properties are especially attractive for a variety of applicatio...
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creator | Cao, Peng‐Fei Li, Bingrui Hong, Tao Townsend, Jacob Qiang, Zhe Xing, Kunyue Vogiatzis, Konstantinos D. Wang, Yangyang Mays, Jimmy W. Sokolov, Alexei P. Saito, Tomonori |
description | Utilization of self‐healing chemistry to develop synthetic polymer materials that can heal themselves with restored mechanical performance and functionality is of great interest. Self‐healable polymer elastomers with tunable mechanical properties are especially attractive for a variety of applications. Herein, a series of urea functionalized poly(dimethyl siloxane)‐based elastomers (U‐PDMS‐Es) are reported with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance. Tailoring the molecular weights of poly(dimethyl siloxane) or weight ratio of elastic cross‐linker offers tunable mechanical properties of the obtained U‐PDMS‐Es, such as ultimate elongation (from 984% to 5600%), Young's modulus, ultimate tensile strength, toughness, and elastic recovery. The U‐PDMS‐Es can serve as excellent acoustic and vibration damping materials over a broad range of temperature (over 100 °C). The strain‐dependent elastic recovery behavior of U‐PDMS‐Es is also studied. After mechanical damage, the U‐PDMS‐Es can be healed in 120 min at ambient temperature or in 20 min at 40 °C with completely restored mechanical performance. The U‐PDMS‐Es are also demonstrated to exhibit recoverable gas‐separation functionality with retained permeability/selectivity after being damaged.
Urea‐functionalized poly(dimethyl siloxane)‐based elastomers with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance are fabricated. Tailoring the molecular weights of poly(dimethyl siloxane) offers tunable mechanical properties, such as ultimate elongation (from 984% to 5600%), Young's modulus, toughness, and elastic recovery. After mechanical damage, the elastomers can be healed in 2 h at ambient temperature with completely restored mechanical properties and recovered gas‐separation functionalities. |
doi_str_mv | 10.1002/adfm.201800741 |
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Urea‐functionalized poly(dimethyl siloxane)‐based elastomers with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance are fabricated. Tailoring the molecular weights of poly(dimethyl siloxane) offers tunable mechanical properties, such as ultimate elongation (from 984% to 5600%), Young's modulus, toughness, and elastic recovery. After mechanical damage, the elastomers can be healed in 2 h at ambient temperature with completely restored mechanical properties and recovered gas‐separation functionalities.</description><identifier>ISSN: 1616-301X</identifier><identifier>EISSN: 1616-3028</identifier><identifier>DOI: 10.1002/adfm.201800741</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Ambient temperature ; Elastic recovery ; Elastomers ; Elongation ; gas separation ; Healing ; hydrogen bonding ; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY ; MATERIALS SCIENCE ; Mechanical properties ; Modulus of elasticity ; Molecular chains ; Polydimethylsiloxane ; polymeric elastomers ; Polymers ; self-healing ; Separation ; Silicone resins ; Strain ; Stretchability ; tunable mechanical properties ; Ultimate tensile strength ; Vibration damping</subject><ispartof>Advanced functional materials, 2018-05, Vol.28 (22), p.n/a</ispartof><rights>2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3841-587e2377ae0f567faa8ed2e424bc22bdbbdae31a3ecf7545959fde123da20ce53</citedby><cites>FETCH-LOGICAL-c3841-587e2377ae0f567faa8ed2e424bc22bdbbdae31a3ecf7545959fde123da20ce53</cites><orcidid>0000-0003-2391-1838 ; 0000000323911838</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadfm.201800741$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadfm.201800741$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.osti.gov/servlets/purl/1435198$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Peng‐Fei</creatorcontrib><creatorcontrib>Li, Bingrui</creatorcontrib><creatorcontrib>Hong, Tao</creatorcontrib><creatorcontrib>Townsend, Jacob</creatorcontrib><creatorcontrib>Qiang, Zhe</creatorcontrib><creatorcontrib>Xing, Kunyue</creatorcontrib><creatorcontrib>Vogiatzis, Konstantinos D.</creatorcontrib><creatorcontrib>Wang, Yangyang</creatorcontrib><creatorcontrib>Mays, Jimmy W.</creatorcontrib><creatorcontrib>Sokolov, Alexei P.</creatorcontrib><creatorcontrib>Saito, Tomonori</creatorcontrib><creatorcontrib>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</creatorcontrib><title>Superstretchable, Self‐Healing Polymeric Elastomers with Tunable Properties</title><title>Advanced functional materials</title><description>Utilization of self‐healing chemistry to develop synthetic polymer materials that can heal themselves with restored mechanical performance and functionality is of great interest. Self‐healable polymer elastomers with tunable mechanical properties are especially attractive for a variety of applications. Herein, a series of urea functionalized poly(dimethyl siloxane)‐based elastomers (U‐PDMS‐Es) are reported with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance. Tailoring the molecular weights of poly(dimethyl siloxane) or weight ratio of elastic cross‐linker offers tunable mechanical properties of the obtained U‐PDMS‐Es, such as ultimate elongation (from 984% to 5600%), Young's modulus, ultimate tensile strength, toughness, and elastic recovery. The U‐PDMS‐Es can serve as excellent acoustic and vibration damping materials over a broad range of temperature (over 100 °C). The strain‐dependent elastic recovery behavior of U‐PDMS‐Es is also studied. After mechanical damage, the U‐PDMS‐Es can be healed in 120 min at ambient temperature or in 20 min at 40 °C with completely restored mechanical performance. The U‐PDMS‐Es are also demonstrated to exhibit recoverable gas‐separation functionality with retained permeability/selectivity after being damaged.
Urea‐functionalized poly(dimethyl siloxane)‐based elastomers with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance are fabricated. Tailoring the molecular weights of poly(dimethyl siloxane) offers tunable mechanical properties, such as ultimate elongation (from 984% to 5600%), Young's modulus, toughness, and elastic recovery. After mechanical damage, the elastomers can be healed in 2 h at ambient temperature with completely restored mechanical properties and recovered gas‐separation functionalities.</description><subject>Ambient temperature</subject><subject>Elastic recovery</subject><subject>Elastomers</subject><subject>Elongation</subject><subject>gas separation</subject><subject>Healing</subject><subject>hydrogen bonding</subject><subject>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</subject><subject>MATERIALS SCIENCE</subject><subject>Mechanical properties</subject><subject>Modulus of elasticity</subject><subject>Molecular chains</subject><subject>Polydimethylsiloxane</subject><subject>polymeric elastomers</subject><subject>Polymers</subject><subject>self-healing</subject><subject>Separation</subject><subject>Silicone resins</subject><subject>Strain</subject><subject>Stretchability</subject><subject>tunable mechanical properties</subject><subject>Ultimate tensile strength</subject><subject>Vibration damping</subject><issn>1616-301X</issn><issn>1616-3028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkM1Kw0AUhYMoWKtb10G3ps5fMsmy1NYKFgut4G6YTG7slDRTZyaU7nwEn9EnMSVSl67uWXzf4XKC4BqjAUaI3Mui3AwIwilCnOGToIcTnEQUkfT0mPHbeXDh3BohzDllvWC2aLZgnbfg1UrmFdyFC6jK78-vKchK1-_h3FT7DVitwnElnTdtduFO-1W4bOqDEc6taTu8BncZnJWycnD1e_vB62S8HE2j55fHp9HwOVI0ZTiKUw6Eci4BlXHCSylTKAgwwnJFSF7keSGBYklBlTxmcRZnZQGY0EISpCCm_eCm6zXOa-GU9qBWytQ1KC8wozHO0ha67aCtNR8NOC_WprF1-5cgiHHWFiespQYdpaxxzkIptlZvpN0LjMRhV3HYVRx3bYWsE3a6gv0_tBg-TGZ_7g8e133c</recordid><startdate>20180530</startdate><enddate>20180530</enddate><creator>Cao, Peng‐Fei</creator><creator>Li, Bingrui</creator><creator>Hong, Tao</creator><creator>Townsend, Jacob</creator><creator>Qiang, Zhe</creator><creator>Xing, Kunyue</creator><creator>Vogiatzis, Konstantinos D.</creator><creator>Wang, Yangyang</creator><creator>Mays, Jimmy W.</creator><creator>Sokolov, Alexei P.</creator><creator>Saito, Tomonori</creator><general>Wiley Subscription Services, Inc</general><general>Wiley</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>OIOZB</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0003-2391-1838</orcidid><orcidid>https://orcid.org/0000000323911838</orcidid></search><sort><creationdate>20180530</creationdate><title>Superstretchable, Self‐Healing Polymeric Elastomers with Tunable Properties</title><author>Cao, Peng‐Fei ; Li, Bingrui ; Hong, Tao ; Townsend, Jacob ; Qiang, Zhe ; Xing, Kunyue ; Vogiatzis, Konstantinos D. ; Wang, Yangyang ; Mays, Jimmy W. ; Sokolov, Alexei P. ; Saito, Tomonori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3841-587e2377ae0f567faa8ed2e424bc22bdbbdae31a3ecf7545959fde123da20ce53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Ambient temperature</topic><topic>Elastic recovery</topic><topic>Elastomers</topic><topic>Elongation</topic><topic>gas separation</topic><topic>Healing</topic><topic>hydrogen bonding</topic><topic>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</topic><topic>MATERIALS SCIENCE</topic><topic>Mechanical properties</topic><topic>Modulus of elasticity</topic><topic>Molecular chains</topic><topic>Polydimethylsiloxane</topic><topic>polymeric elastomers</topic><topic>Polymers</topic><topic>self-healing</topic><topic>Separation</topic><topic>Silicone resins</topic><topic>Strain</topic><topic>Stretchability</topic><topic>tunable mechanical properties</topic><topic>Ultimate tensile strength</topic><topic>Vibration damping</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Peng‐Fei</creatorcontrib><creatorcontrib>Li, Bingrui</creatorcontrib><creatorcontrib>Hong, Tao</creatorcontrib><creatorcontrib>Townsend, Jacob</creatorcontrib><creatorcontrib>Qiang, Zhe</creatorcontrib><creatorcontrib>Xing, Kunyue</creatorcontrib><creatorcontrib>Vogiatzis, Konstantinos D.</creatorcontrib><creatorcontrib>Wang, Yangyang</creatorcontrib><creatorcontrib>Mays, Jimmy W.</creatorcontrib><creatorcontrib>Sokolov, Alexei P.</creatorcontrib><creatorcontrib>Saito, Tomonori</creatorcontrib><creatorcontrib>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Advanced functional materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Peng‐Fei</au><au>Li, Bingrui</au><au>Hong, Tao</au><au>Townsend, Jacob</au><au>Qiang, Zhe</au><au>Xing, Kunyue</au><au>Vogiatzis, Konstantinos D.</au><au>Wang, Yangyang</au><au>Mays, Jimmy W.</au><au>Sokolov, Alexei P.</au><au>Saito, Tomonori</au><aucorp>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Superstretchable, Self‐Healing Polymeric Elastomers with Tunable Properties</atitle><jtitle>Advanced functional materials</jtitle><date>2018-05-30</date><risdate>2018</risdate><volume>28</volume><issue>22</issue><epage>n/a</epage><issn>1616-301X</issn><eissn>1616-3028</eissn><abstract>Utilization of self‐healing chemistry to develop synthetic polymer materials that can heal themselves with restored mechanical performance and functionality is of great interest. Self‐healable polymer elastomers with tunable mechanical properties are especially attractive for a variety of applications. Herein, a series of urea functionalized poly(dimethyl siloxane)‐based elastomers (U‐PDMS‐Es) are reported with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance. Tailoring the molecular weights of poly(dimethyl siloxane) or weight ratio of elastic cross‐linker offers tunable mechanical properties of the obtained U‐PDMS‐Es, such as ultimate elongation (from 984% to 5600%), Young's modulus, ultimate tensile strength, toughness, and elastic recovery. The U‐PDMS‐Es can serve as excellent acoustic and vibration damping materials over a broad range of temperature (over 100 °C). The strain‐dependent elastic recovery behavior of U‐PDMS‐Es is also studied. After mechanical damage, the U‐PDMS‐Es can be healed in 120 min at ambient temperature or in 20 min at 40 °C with completely restored mechanical performance. The U‐PDMS‐Es are also demonstrated to exhibit recoverable gas‐separation functionality with retained permeability/selectivity after being damaged.
Urea‐functionalized poly(dimethyl siloxane)‐based elastomers with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance are fabricated. Tailoring the molecular weights of poly(dimethyl siloxane) offers tunable mechanical properties, such as ultimate elongation (from 984% to 5600%), Young's modulus, toughness, and elastic recovery. After mechanical damage, the elastomers can be healed in 2 h at ambient temperature with completely restored mechanical properties and recovered gas‐separation functionalities.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adfm.201800741</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2391-1838</orcidid><orcidid>https://orcid.org/0000000323911838</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Ambient temperature Elastic recovery Elastomers Elongation gas separation Healing hydrogen bonding INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY MATERIALS SCIENCE Mechanical properties Modulus of elasticity Molecular chains Polydimethylsiloxane polymeric elastomers Polymers self-healing Separation Silicone resins Strain Stretchability tunable mechanical properties Ultimate tensile strength Vibration damping |
title | Superstretchable, Self‐Healing Polymeric Elastomers with Tunable Properties |
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