Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers
Inspired by the growing demand for smart and environmentally friendly polymer materials, we employed 2,2′-disulfanediyldianiline (22DTDA) as a chain extender to synthesize a waterborne polyurethane (WPUR). Due to the ortho-substituted structure of the aromatic disulfide, the urea moieties formed a u...
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MDPI AG
2020-04-01
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Series: | Polymers |
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Online Access: | https://www.mdpi.com/2073-4360/12/4/989 |
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author | Liangdong Zhang Teng Qiu Xiting Sun Longhai Guo Lifan He Jun Ye Xiaoyu Li |
author_facet | Liangdong Zhang Teng Qiu Xiting Sun Longhai Guo Lifan He Jun Ye Xiaoyu Li |
author_sort | Liangdong Zhang |
collection | DOAJ |
description | Inspired by the growing demand for smart and environmentally friendly polymer materials, we employed 2,2′-disulfanediyldianiline (22DTDA) as a chain extender to synthesize a waterborne polyurethane (WPUR). Due to the ortho-substituted structure of the aromatic disulfide, the urea moieties formed a unique microphase structure in the WPUR, its mechanical strength was enhanced more 180 times relative to that of the material prepared without 22DTDA, and excellent self-healing abilities at body temperature in air or under ultrasound in water were obtained. If the self-healing process was carried out at 37 °C, 50 °C or under ultrasound, the ultimate tensile strength and elongation at break of the healed film could reach 13.8 MPa and 1150%, 15.4 MPa and 1215%, or 16 MPa and 1056%, respectively. Moreover, the WPUR films could be re-healed at the same fracture location over three cutting–healing cycles, and the recovery rates of the tensile strength and elongation at break remained almost constant throughout these cycles. |
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language | English |
last_indexed | 2024-03-10T20:15:54Z |
publishDate | 2020-04-01 |
publisher | MDPI AG |
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series | Polymers |
spelling | doaj.art-df06b13ea4ee4dec8c27b36f414879af2023-11-19T22:35:45ZengMDPI AGPolymers2073-43602020-04-0112498910.3390/polym12040989Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne PolymersLiangdong Zhang0Teng Qiu1Xiting Sun2Longhai Guo3Lifan He4Jun Ye5Xiaoyu Li6State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, ChinaState Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, ChinaState Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, ChinaState Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, ChinaBeijing Engineering Research Center of Synthesis and Application of Waterborne Polymer, Beijing University of Chemical Technology, Beijing 100029, ChinaBeijing Engineering Research Center of Synthesis and Application of Waterborne Polymer, Beijing University of Chemical Technology, Beijing 100029, ChinaState Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, ChinaInspired by the growing demand for smart and environmentally friendly polymer materials, we employed 2,2′-disulfanediyldianiline (22DTDA) as a chain extender to synthesize a waterborne polyurethane (WPUR). Due to the ortho-substituted structure of the aromatic disulfide, the urea moieties formed a unique microphase structure in the WPUR, its mechanical strength was enhanced more 180 times relative to that of the material prepared without 22DTDA, and excellent self-healing abilities at body temperature in air or under ultrasound in water were obtained. If the self-healing process was carried out at 37 °C, 50 °C or under ultrasound, the ultimate tensile strength and elongation at break of the healed film could reach 13.8 MPa and 1150%, 15.4 MPa and 1215%, or 16 MPa and 1056%, respectively. Moreover, the WPUR films could be re-healed at the same fracture location over three cutting–healing cycles, and the recovery rates of the tensile strength and elongation at break remained almost constant throughout these cycles.https://www.mdpi.com/2073-4360/12/4/989disulfideself-healingwaterborne polyurethane |
spellingShingle | Liangdong Zhang Teng Qiu Xiting Sun Longhai Guo Lifan He Jun Ye Xiaoyu Li Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers Polymers disulfide self-healing waterborne polyurethane |
title | Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers |
title_full | Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers |
title_fullStr | Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers |
title_full_unstemmed | Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers |
title_short | Achievement of Both Mechanical Properties and Intrinsic Self-Healing under Body Temperature in Polyurethane Elastomers: A Synthesis Strategy from Waterborne Polymers |
title_sort | achievement of both mechanical properties and intrinsic self healing under body temperature in polyurethane elastomers a synthesis strategy from waterborne polymers |
topic | disulfide self-healing waterborne polyurethane |
url | https://www.mdpi.com/2073-4360/12/4/989 |
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