scholarly journals Unveiling the molecular mechanism of self-healing in a telechelic, supramolecular polymer network

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Tingzi Yan ◽  
Klaus Schröter ◽  
Florian Herbst ◽  
Wolfgang H. Binder ◽  
Thomas Thurn-Albrecht
2018 ◽  
Vol 9 (16) ◽  
pp. 2087-2091 ◽  
Author(s):  
Wenbo Wang ◽  
Hao Xing

A novel supramolecular mechanically interlocked crosslinker was designed and used to prepare a supramolecular polymer network.


2020 ◽  
Vol 117 (14) ◽  
pp. 7606-7612 ◽  
Author(s):  
Xueyu Li ◽  
Kunpeng Cui ◽  
Tao Lin Sun ◽  
Lingpu Meng ◽  
Chengtao Yu ◽  
...  

Load-bearing biological tissues, such as muscles, are highly fatigue-resistant, but how the exquisite hierarchical structures of biological tissues contribute to their excellent fatigue resistance is not well understood. In this work, we study antifatigue properties of soft materials with hierarchical structures using polyampholyte hydrogels (PA gels) as a simple model system. PA gels are tough and self-healing, consisting of reversible ionic bonds at the 1-nm scale, a cross-linked polymer network at the 10-nm scale, and bicontinuous hard/soft phase networks at the 100-nm scale. We find that the polymer network at the 10-nm scale determines the threshold of energy release rateG0above which the crack grows, while the bicontinuous phase networks at the 100-nm scale significantly decelerate the crack advance until a transitionGtranfar aboveG0. In situ small-angle X-ray scattering analysis reveals that the hard phase network suppresses the crack advance to show decelerated fatigue fracture, andGtrancorresponds to the rupture of the hard phase network.


2017 ◽  
Vol 38 (5) ◽  
pp. 1600702 ◽  
Author(s):  
Chih-Chia Cheng ◽  
Wei-Tsung Chuang ◽  
Duu-Jong Lee ◽  
Zhong Xin ◽  
Chih-Wei Chiu

2013 ◽  
Vol 4 (11) ◽  
pp. 3312 ◽  
Author(s):  
Xuzhou Yan ◽  
Donghua Xu ◽  
Jianzhuang Chen ◽  
Mingming Zhang ◽  
Bingjie Hu ◽  
...  

RSC Advances ◽  
2018 ◽  
Vol 8 (31) ◽  
pp. 17044-17055 ◽  
Author(s):  
Tuhin Ghosh ◽  
Niranjan Karak

A tough IPN of silicone containing polyurethane and polystyrene with smart attributes like self-healing, shape memory and self-cleaning is reported.


Soft Matter ◽  
2018 ◽  
Vol 14 (42) ◽  
pp. 8529-8536 ◽  
Author(s):  
You-Ming Zhang ◽  
Yong-Fu Li ◽  
Hu Fang ◽  
Jun-Xia He ◽  
Bi-Rong Yong ◽  
...  

A novel pseudorotaxanes-type crosslinker of a supramolecular polymer network (WP5-PN) was constructed based on water-soluble pillar[5]arene (WP5) and naphthalene dimethylamine derivative (PN) via host-guest interactions.


2019 ◽  
Vol 132 ◽  
pp. 374-384 ◽  
Author(s):  
Alina Gabriela Rusu ◽  
Aurica P. Chiriac ◽  
Loredana Elena Nita ◽  
Maria Bercea ◽  
Nita Tudorachi ◽  
...  

Polymers ◽  
2018 ◽  
Vol 11 (1) ◽  
pp. 41 ◽  
Author(s):  
Ali Berkem ◽  
Ahmet Capoglu ◽  
Turgut Nugay ◽  
Erol Sancaktar ◽  
Ilke Anac

The self-healing ability can be imparted to the polymers by different mechanisms. In this study, self-healing polydimethylsiloxane-graft-polyurethane (PDMS-g-PUR)/Vanadium pentoxide (V2O5) nanofiber supramolecular polymer composites based on a reversible hydrogen bonding mechanism are prepared. V2O5 nanofibers are synthesized via colloidal route and characterized by XRD, SEM, EDX, and TEM techniques. In order to prepare PDMS-g-PUR, linear aliphatic PUR having one –COOH functional group (PUR-COOH) is synthesized and grafted onto aminopropyl functionalized PDMS by EDC/HCl coupling reaction. PUR-COOH and PDMS-g-PUR are characterized by 1H NMR, FTIR. PDMS-g-PUR/V2O5 nanofiber composites are prepared and characterized by DSC/TGA, FTIR, and tensile tests. The self-healing ability of PDMS-graft-PUR and composites are determined by mechanical tests and optical microscope. Tensile strength data obtained from mechanical tests show that healing efficiencies of PDMS-g-PUR increase with healing time and reach 85.4 ± 1.2 % after waiting 120 min at 50 °C. The addition of V2O5 nanofibers enhances the mechanical properties and healing efficiency of the PDMS-g-PUR. An increase of healing efficiency and max tensile strength from 85.4 ± 1.2% to 95.3 ± 0.4% and 113.08 ± 5.24 kPa to 1443.40 ± 8.96 kPa is observed after the addition of 10 wt % V2O5 nanofiber into the polymer.


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