Effects of Hard Segment of Polyurethane with Disulfide Bonds on Shape Memory and Self-Healing Ability

被引:26
作者
Ha, Yu-Mi [1 ,2 ]
Seo, Hae Cheon [3 ]
Kim, Young-O [1 ]
Khil, Myung-Seob [3 ]
Cho, Jae Whan [4 ]
Lee, Jae-Suk [2 ]
Jung, Yong Chae [1 ]
机构
[1] KIST, Inst Adv Composite Mat, 92 Chudong Ro, Wanju Gun 55324, Jeonbuk, South Korea
[2] GIST, Sch Mat Sci & Engn, 123 Cheomdangwagi Ro, Gwangju 61005, South Korea
[3] Chonbuk Natl Univ, Dept Organ Mat & Fiber Engn, 567 Baekje Daero, Jeonju Si 56896, Jeonbuk, South Korea
[4] Konkuk Univ, Dept Organ & Nano Syst Engn, Seoul 05029, South Korea
关键词
Polyurethane; phase separation; self-healing shape memory; polycarbonate; THERMOMECHANICAL PROPERTIES; BLOCK-COPOLYMERS; MORPHOLOGY; BEHAVIOR; POLYMER; FTIR; PCL;
D O I
10.1007/s13233-020-8027-y
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Self-healing polyurethane with disulfide bonds was synthesized using polycarbonate diol as a soft segment, and methylene diphenyl diisocyanate and 2-hydroxyethyl disulfide as a hard segment. Well-developed phase separation as the hard segments increased was confirmed by Fourier transform infrared spectra. The X-ray diffraction data showed that the crystallinity of the polycarbonate with a semicrystalline structure decreased as the HS increased, which affected the thermal, mechanical, and thermomechanical properties of the PU block copolymer. As the hard segments increased, the yield point on the strain-stress curve disappeared, and the mechanical properties (elongation at break and breaking stress) and the shape recovery rate of SHPU improved. The increase in the physical crosslinking between the hard segments contributed to improving shape recovery and mechanical properties. In particular, self-healing polyurethane with 30, and 35 wt% hard segments showed excellent self-healing ability at 80 C, while the self-healing ability for self-healing polyurethane with 40 wt% hard segments was decreased. The increase of the hard segment restricted the movement of the soft segment, thus the self-healing ability of SHPU with 40 wt% HS was decreased. It could be concluded that self-healing polyurethane synthesized using semicrystalline PC diol has a significant effect on shape recovery and self-healing efficiency due to the crosslinks between the hard segments.
引用
收藏
页码:234 / 240
页数:7
相关论文
共 33 条
[1]  
Aguilar MR, 2014, WOODHEAD PUBL MATER, P1, DOI 10.1533/9780857097026.1
[2]   Aromatic disulfide crosslinks in polymer systems: Self-healing, reprocessability, recyclability and more [J].
Azcune, Itxaso ;
Odriozola, Ibon .
EUROPEAN POLYMER JOURNAL, 2016, 84 :147-160
[3]   Self-Healing Materials Based on Disulfide Links [J].
Canadell, Judit ;
Goossens, Han ;
Klumperman, Bert .
MACROMOLECULES, 2011, 44 (08) :2536-2541
[4]   Autonomous Deployment of a Solar Panel Using Elastic Origami and Distributed Shape-Memory-Polymer Actuators [J].
Chen, Tian ;
Bilal, Osama R. ;
Lang, Robert ;
Daraio, Chiara ;
Shea, Kristina .
PHYSICAL REVIEW APPLIED, 2019, 11 (06)
[5]   Synthesis and characterization of novel segmented polyurethane/clay nanocomposites [J].
Chen, TK ;
Tien, YI ;
Wei, KH .
POLYMER, 2000, 41 (04) :1345-1353
[6]   Electroactive shape-memory polyurethane composites incorporating carbon nanotubes [J].
Cho, JW ;
Kim, JW ;
Jung, YC ;
Goo, NS .
MACROMOLECULAR RAPID COMMUNICATIONS, 2005, 26 (05) :412-416
[7]   Affect of polydispersity on the properties of waterborne polyurethane dispersions based on polycarbonate polyol [J].
Garcia-Pacios, Vanesa ;
Costa, Victor ;
Colera, Manuel ;
Miguel Martin-Martinez, Jose .
INTERNATIONAL JOURNAL OF ADHESION AND ADHESIVES, 2010, 30 (06) :456-465
[8]   Phase separation of diamine chain-extended poly(urethane) copolymers: FTIR spectroscopy and phase transitions [J].
Garrett, JT ;
Xu, RJ ;
Cho, JD ;
Runt, J .
POLYMER, 2003, 44 (09) :2711-2719
[9]   Self-Healing Polyurethanes with Shape Recovery [J].
Heo, Yunseon ;
Sodano, Henry A. .
ADVANCED FUNCTIONAL MATERIALS, 2014, 24 (33) :5261-5268
[10]   Self-healing polyurethane based on disulfide bond and hydrogen bond [J].
Jian, Xiaoxia ;
Hu, Yiwen ;
Zhou, Weiliang ;
Xiao, Leqin .
POLYMERS FOR ADVANCED TECHNOLOGIES, 2018, 29 (01) :463-469