Synthesis and properties of strong and tough Diels–Alder self-healing crosslinked polyamides

2021 ◽  
Vol 28 (4) ◽  
Author(s):  
Jinnan Zhao ◽  
Shuo Chen ◽  
Jingbo Zhao ◽  
Zhiyuan Zhang ◽  
Junying Zhang
Keyword(s):  
Diels Alder ◽  
Self Healing

Self-Healing Hydrophobic POSS-functionalized Fluorinated Copolymer via RAFT Polymerization and dynamic Diels-Alder Reaction

2021 ◽  
Author(s):  
Siva Ponnupandian ◽  
Prantik Mondal ◽  
Thomas Becker ◽  
Richard Hoogenboom ◽  
Andrew B Lowe ◽  
...  
Keyword(s):  
Chain Transfer ◽  
Raft Polymerization ◽  
Alder Reaction ◽  
Diels Alder ◽  
Self Healing ◽  
Diels Alder Reaction ◽  
Reversible Addition

This investigation reports the preparation of a tailor-made copolymer of furfuryl methacrylate (FMA) and trifluoroethyl methacrylate (TFEMA) via reversible addition-fragmentation chain transfer (RAFT) polymerization. The furfuryl groups of the copolymer...

Self-healing poly(siloxane-urethane) elastomers with remoldability, shape memory and biocompatibility

2016 ◽  
Vol 7 (47) ◽  
pp. 7278-7286 ◽  
Author(s):  
Jian Zhao ◽  
Rui Xu ◽  
Gaoxing Luo ◽  
Jun Wu ◽  
Hesheng Xia
Keyword(s):  
Mechanical Property ◽  
Shape Memory ◽  
Microphase Separation ◽  
Diels Alder ◽  
Good Mechanical Property ◽  
Self Healing ◽  
Healing Efficiency ◽  
Good Biocompatibility

The poly(siloxane-urethane) elastomers with microphase separation structure and Diels–Alder bonds show high healing efficiency, good mechanical property and good biocompatibility.

Fast‐reprocessing, Post‐adjustable, Self‐healing Covalent Adaptable Networks with Schiff base and Diels‐Alder Adduct

2022 ◽  
pp. 2100777
Author(s):  
Xiwei Xu ◽  
Songqi Ma ◽  
Sheng Wang ◽  
Binbo Wang ◽  
Hongzhi Feng ◽  
...  
Keyword(s):  
Schiff Base ◽  
Diels Alder ◽  
Self Healing ◽  
Alder Adduct

Self-healable Functional Polymers based on Diels-Alder ‘Click Chemistry’ Involving Substituted Furan and Triazolinedione Derivatives; A Simple and Very Fast Approach

2021 ◽  
Author(s):  
Prantik Mondal ◽  
Gourhari Jana ◽  
Tuhin Subhra Pal ◽  
Pratim K. Chattaraj ◽  
Nikhil K Singha
Keyword(s):  
Click Chemistry ◽  
Materials Science ◽  
Functional Polymers ◽  
Diels Alder ◽  
Polymer Materials ◽  
Self Healing ◽  
Natural Phenomena ◽  
Science And Engineering ◽  
Fast Approach ◽  
Materials Science And Engineering

Nowadays, the design of functional polymer materials that can mimic natural phenomena, e.g., self-healing of skin cuts, has got a tremendous interest in materials science and engineering. Recently, 1,2,4-triazoline-3,5-dione (TAD)...

scholarly journals A review on Diels-Alder based self-healing polymer composites

2018 ◽  
Vol 377 ◽  
pp. 012007 ◽  
Author(s):  
N I Khan ◽  
S Halder ◽  
S B Gunjan ◽  
T Prasad
Keyword(s):  
Polymer Composites ◽  
Diels Alder ◽  
Self Healing

The influence of furanyl monomer on the self-healing polyurethanes by reverse Diels-Alder cross-link

2018 ◽  
Vol 30 (3) ◽  
pp. 804-807 ◽  
Author(s):  
Yunlin Pan ◽  
Xi Yu ◽  
Pengfei Yang ◽  
Junying Li ◽  
Datong Zhang ◽  
...  
Keyword(s):  
Diels Alder ◽  
The Self ◽  
Self Healing ◽  
Cross Link

Self-healing 8-armed star-shaped ɛ-caprolactone oligomers dually crosslinked by the Diels-Alder and urethanization reactions

Polymer ◽  
2018 ◽  
Vol 144 ◽  
pp. 92-102 ◽  
Author(s):  
Kaito Sugane ◽  
Yoshiki Yoshioka ◽  
Toshiaki Shimasaki ◽  
Naozumi Teramoto ◽  
Mitsuhiro Shibata
Keyword(s):  
Diels Alder ◽  
Self Healing

New Chain Extenders for Self-Healing Polymers

2021 ◽  
Vol 899 ◽  
pp. 628-637
Author(s):  
Daria V. Zakharova ◽  
Zalina A. Lok’yaeva ◽  
Alexander A. Pavlov ◽  
Alexander V. Polezhaev
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Hydroxyl Groups ◽  
Structural Fragment ◽  
Self Healing ◽  
Diels Alder Reaction ◽  
Small Series ◽  
Chain Extenders ◽  
Reversible Covalent ◽  
Thermochemical Parameters

We present here a small series of compounds designed to modify the polymer chain of various polyurethanes in order to introduce a structural fragment with the ability of thermally-triggered reversible covalent interactions. Bismaleimides (2a-2e) were synthesized from commercially available aromatic and aliphatic symmetric diamines (1a-1e) and were further introduced into the Diels-Alder reaction with furfuryl alcohol as dienophiles. The Diels-Alder adducts (3a-3e) were obtained as a mixture of endo- and exo-isomer. The presence of symmetrical hydroxyl groups in the structure of the obtained compounds makes them suitable as chain extenders of low molecular weight diisocyanate prepolymers. The presence of a thermally reversible Diels-Alder reaction adduct in the structure of potential chain-extenders opens a possibility to create unique materials with self-healing properties. All compounds obtained were characterized by 1H, 13C NMR, ESI-HRMS, and IR spectroscopy. The thermochemical parameters of the reverse Diels-Alder reaction were established using DSC analysis.

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