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A facile method to fabricate tough hydrogel with ultra‐wide adjustable stiffness, stress, and fast recoverability
ABSTRACT In this article, we report a synergistic strategy to develop dual physically cross‐linked tough hydrogels via one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone, acrylic acid, and stearyl methylacrylate (SMA) without any adscititious surfactant. Due to synergic effects of hydrogen bondi...
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Published in: | Journal of polymer science. Part B, Polymer physics Polymer physics, 2018-11, Vol.56 (21), p.1469-1474 |
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creator | Xiang, Shuangfei Li, Ting Dong, Weifu Lu, Qinghua |
description | ABSTRACT
In this article, we report a synergistic strategy to develop dual physically cross‐linked tough hydrogels via one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone, acrylic acid, and stearyl methylacrylate (SMA) without any adscititious surfactant. Due to synergic effects of hydrogen bonding and hydrophobic association, the resulted dual physically cross‐linked hydrogels (DP Gel) with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), and toughness (3.3–23.1 MJ m−3). Stretching to 300%, DP Gel exhibited fast recoverability that remained ~95% of initial dissipated energy after resting in 60 °C for 3 min. Finally, scanning electron microscopy revealed that the microstructure of hydrogel changed from phase separation structure to micro phase separation as SMA added, which accounted for excellent performance of DP Gel. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018, 56, 1469–1474
A facile method to fabricate dual physically cross‐linked hydrogels with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), toughness (3.3–23.1 MJ·m−3), and fast recoverability is presented. The hydrogel was developed via a one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone (NVP), acrylic acid (AAc), and stearyl methylacrylate (SMA) without any added surfactant. |
doi_str_mv | 10.1002/polb.24737 |
format | article |
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In this article, we report a synergistic strategy to develop dual physically cross‐linked tough hydrogels via one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone, acrylic acid, and stearyl methylacrylate (SMA) without any adscititious surfactant. Due to synergic effects of hydrogen bonding and hydrophobic association, the resulted dual physically cross‐linked hydrogels (DP Gel) with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), and toughness (3.3–23.1 MJ m−3). Stretching to 300%, DP Gel exhibited fast recoverability that remained ~95% of initial dissipated energy after resting in 60 °C for 3 min. Finally, scanning electron microscopy revealed that the microstructure of hydrogel changed from phase separation structure to micro phase separation as SMA added, which accounted for excellent performance of DP Gel. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018, 56, 1469–1474
A facile method to fabricate dual physically cross‐linked hydrogels with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), toughness (3.3–23.1 MJ·m−3), and fast recoverability is presented. The hydrogel was developed via a one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone (NVP), acrylic acid (AAc), and stearyl methylacrylate (SMA) without any added surfactant.</description><identifier>ISSN: 0887-6266</identifier><identifier>EISSN: 1099-0488</identifier><identifier>DOI: 10.1002/polb.24737</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Acrylic acid ; Copolymerization ; Hydrogels ; Hydrogen bonding ; hydrogen bonds ; hydrophobic association ; mechanical properties ; Modulus of elasticity ; Phase separation ; Phase transitions ; Recoverability ; Scanning electron microscopy ; Stiffness ; Tensile stress ; tough hydrogels</subject><ispartof>Journal of polymer science. Part B, Polymer physics, 2018-11, Vol.56 (21), p.1469-1474</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3017-e26c043185bc0b19a24c0ccb6d8a53a78131afaaf8aa43e7b867222150413df73</citedby><cites>FETCH-LOGICAL-c3017-e26c043185bc0b19a24c0ccb6d8a53a78131afaaf8aa43e7b867222150413df73</cites><orcidid>0000-0002-7432-8362</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Xiang, Shuangfei</creatorcontrib><creatorcontrib>Li, Ting</creatorcontrib><creatorcontrib>Dong, Weifu</creatorcontrib><creatorcontrib>Lu, Qinghua</creatorcontrib><title>A facile method to fabricate tough hydrogel with ultra‐wide adjustable stiffness, stress, and fast recoverability</title><title>Journal of polymer science. Part B, Polymer physics</title><description>ABSTRACT
In this article, we report a synergistic strategy to develop dual physically cross‐linked tough hydrogels via one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone, acrylic acid, and stearyl methylacrylate (SMA) without any adscititious surfactant. Due to synergic effects of hydrogen bonding and hydrophobic association, the resulted dual physically cross‐linked hydrogels (DP Gel) with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), and toughness (3.3–23.1 MJ m−3). Stretching to 300%, DP Gel exhibited fast recoverability that remained ~95% of initial dissipated energy after resting in 60 °C for 3 min. Finally, scanning electron microscopy revealed that the microstructure of hydrogel changed from phase separation structure to micro phase separation as SMA added, which accounted for excellent performance of DP Gel. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018, 56, 1469–1474
A facile method to fabricate dual physically cross‐linked hydrogels with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), toughness (3.3–23.1 MJ·m−3), and fast recoverability is presented. The hydrogel was developed via a one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone (NVP), acrylic acid (AAc), and stearyl methylacrylate (SMA) without any added surfactant.</description><subject>Acrylic acid</subject><subject>Copolymerization</subject><subject>Hydrogels</subject><subject>Hydrogen bonding</subject><subject>hydrogen bonds</subject><subject>hydrophobic association</subject><subject>mechanical properties</subject><subject>Modulus of elasticity</subject><subject>Phase separation</subject><subject>Phase transitions</subject><subject>Recoverability</subject><subject>Scanning electron microscopy</subject><subject>Stiffness</subject><subject>Tensile stress</subject><subject>tough hydrogels</subject><issn>0887-6266</issn><issn>1099-0488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kEtOwzAURS0EEqUwYQWRmCFS_EliZ1gQP6lSGcDYenac1lXaFNuhyowlsEZWgtswZvR-594nXYQuCZ4QjOnttm3UhGac8SM0IrgsU5wJcYxGWAieFrQoTtGZ9yuM4y0vR8hPkxq0bUyyNmHZVklo40I5qyGYOHSLZbLsK9cuTJPsbFgmXRMc_Hx972xlEqhWnQ-got4HW9cb4_1NbN2hwqaKZj4kzuj20zhQtrGhP0cnNTTeXPzVMXp_fHi7f05n86eX--ks1QwTnhpaaJwxInKlsSIl0ExjrVVRCcgZcEEYgRqgFgAZM1yJglNKSY4zwqqaszG6Gny3rv3ojA9y1XZuE19KSigXHGe8iNT1QGnXeu9MLbfOrsH1kmC5D1XuQ5WHUCNMBngXI-v_IeXrfHY3aH4Bat18Ow</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Xiang, Shuangfei</creator><creator>Li, Ting</creator><creator>Dong, Weifu</creator><creator>Lu, Qinghua</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-7432-8362</orcidid></search><sort><creationdate>20181101</creationdate><title>A facile method to fabricate tough hydrogel with ultra‐wide adjustable stiffness, stress, and fast recoverability</title><author>Xiang, Shuangfei ; Li, Ting ; Dong, Weifu ; Lu, Qinghua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3017-e26c043185bc0b19a24c0ccb6d8a53a78131afaaf8aa43e7b867222150413df73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acrylic acid</topic><topic>Copolymerization</topic><topic>Hydrogels</topic><topic>Hydrogen bonding</topic><topic>hydrogen bonds</topic><topic>hydrophobic association</topic><topic>mechanical properties</topic><topic>Modulus of elasticity</topic><topic>Phase separation</topic><topic>Phase transitions</topic><topic>Recoverability</topic><topic>Scanning electron microscopy</topic><topic>Stiffness</topic><topic>Tensile stress</topic><topic>tough hydrogels</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiang, Shuangfei</creatorcontrib><creatorcontrib>Li, Ting</creatorcontrib><creatorcontrib>Dong, Weifu</creatorcontrib><creatorcontrib>Lu, Qinghua</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of polymer science. Part B, Polymer physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiang, Shuangfei</au><au>Li, Ting</au><au>Dong, Weifu</au><au>Lu, Qinghua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A facile method to fabricate tough hydrogel with ultra‐wide adjustable stiffness, stress, and fast recoverability</atitle><jtitle>Journal of polymer science. Part B, Polymer physics</jtitle><date>2018-11-01</date><risdate>2018</risdate><volume>56</volume><issue>21</issue><spage>1469</spage><epage>1474</epage><pages>1469-1474</pages><issn>0887-6266</issn><eissn>1099-0488</eissn><abstract>ABSTRACT
In this article, we report a synergistic strategy to develop dual physically cross‐linked tough hydrogels via one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone, acrylic acid, and stearyl methylacrylate (SMA) without any adscititious surfactant. Due to synergic effects of hydrogen bonding and hydrophobic association, the resulted dual physically cross‐linked hydrogels (DP Gel) with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), and toughness (3.3–23.1 MJ m−3). Stretching to 300%, DP Gel exhibited fast recoverability that remained ~95% of initial dissipated energy after resting in 60 °C for 3 min. Finally, scanning electron microscopy revealed that the microstructure of hydrogel changed from phase separation structure to micro phase separation as SMA added, which accounted for excellent performance of DP Gel. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018, 56, 1469–1474
A facile method to fabricate dual physically cross‐linked hydrogels with ultra‐wide range adjustable Young's modulus (0.08–45.6 MPa), tensile stress (0.7–6.9 MPa), toughness (3.3–23.1 MJ·m−3), and fast recoverability is presented. The hydrogel was developed via a one‐pot bulk copolymerization of N‐vinyl‐2‐pyrrolidone (NVP), acrylic acid (AAc), and stearyl methylacrylate (SMA) without any added surfactant.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/polb.24737</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-7432-8362</orcidid></addata></record> |
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subjects | Acrylic acid Copolymerization Hydrogels Hydrogen bonding hydrogen bonds hydrophobic association mechanical properties Modulus of elasticity Phase separation Phase transitions Recoverability Scanning electron microscopy Stiffness Tensile stress tough hydrogels |
title | A facile method to fabricate tough hydrogel with ultra‐wide adjustable stiffness, stress, and fast recoverability |
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