A room-temperature self-healing elastomer with ultra-high strength and toughness fabricated via optimized hierarchical hydrogen-bonding interactions

2022 ◽  
Author(s):  
Liangliang Xia ◽  
Ming Zhou ◽  
Hongjun Tu ◽  
wen Zeng ◽  
xiaoling Yang ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Mechanical Strength ◽  
Room Temperature ◽  
Polymeric Materials ◽  
High Strength ◽  
Self Healing ◽  
High Mechanical Strength ◽  
Hydrogen Bonding Interactions ◽  
Healing Efficiency ◽  
Good Healing

The preparation of room-temperature self-healing polymeric materials with good healing efficiency and high mechanical strength is challenging. Two processes are essential to realise the room-temperature self-healing of materials: (a) a...

Developing self-healable and antibacterial polyacrylate coatings with high mechanical strength through crosslinking by multi-amine hyperbranched polysiloxane via dynamic vinylogous urethane

2017 ◽  
Vol 5 (32) ◽  
pp. 16889-16897 ◽  
Author(s):  
Youhao Zhang ◽  
Li Yuan ◽  
Qingbao Guan ◽  
Guozheng Liang ◽  
Aijuan Gu
Keyword(s):  
Tensile Strength ◽  
Mechanical Strength ◽  
Self Healing ◽  
High Tensile Strength ◽  
High Mechanical Strength ◽  
Antibacterial Ability ◽  
Healing Efficiency ◽  
Hyperbranched Polysiloxane

A novel multi-functional polyacrylate coating simultaneously showing high tensile strength, good reversible self-healing efficiency and remarkable antibacterial ability has been developed.

scholarly journals A Brief Overview on Preparation of Self-Healing Polymers and Coatings via Hydrogen Bonding Interactions

Macromol ◽  
2020 ◽  
Vol 1 (1) ◽  
pp. 18-36
Author(s):  
Ikhlas Gadwal
Keyword(s):  
Mechanical Property ◽  
Hydrogen Bonding ◽  
Service Life ◽  
Review Article ◽  
Main Topic ◽  
Self Healing ◽  
Paint Coating ◽  
Hydrogen Bonding Interactions ◽  
Healing Efficiency

Self-healing coatings or materials have received significant importance in paint, coating, and other industries, as well as in academia, because of their capability to extend materials service life, improving protection, and ensuring sustainability. This review article emphasizes significant advances accomplished in the preparation and properties of intrinsic self-healing materials exclusively based on hydrogen bonding interactions, with possible applications in coatings and adhesives. The main topic of discussion in this review article is the preparation, healing conditions, healing efficiency, and mechanical property recovery after healing. The last part of the review discusses the conclusions and outlook of self-healing materials.

scholarly journals Dynamic Nanohybrid-Polysaccharide Hydrogels for Soft Wearable Strain Sensing

Sensors ◽  
2021 ◽  
Vol 21 (11) ◽  
pp. 3574
Author(s):  
Pejman Heidarian ◽  
Hossein Yousefi ◽  
Akif Kaynak ◽  
Mariana Paulino ◽  
Saleh Gharaie ◽  
...  
Keyword(s):  
Mechanical Strength ◽  
Strain Sensors ◽  
Self Healing ◽  
Nano Materials ◽  
Strain Sensing ◽  
Ferric Ions ◽  
Research Activity ◽  
Adhesion Properties ◽  
High Mechanical Strength ◽  
The Moment

Electroconductive hydrogels with stimuli-free self-healing and self-recovery (SELF) properties and high mechanical strength for wearable strain sensors is an area of intensive research activity at the moment. Most electroconductive hydrogels, however, consist of static bonds for mechanical strength and dynamic bonds for SELF performance, presenting a challenge to improve both properties into one single hydrogel. An alternative strategy to successfully incorporate both properties into one system is via the use of stiff or rigid, yet dynamic nano-materials. In this work, a nano-hybrid modifier derived from nano-chitin coated with ferric ions and tannic acid (TA/Fe@ChNFs) is blended into a starch/polyvinyl alcohol/polyacrylic acid (St/PVA/PAA) hydrogel. It is hypothesized that the TA/Fe@ChNFs nanohybrid imparts both mechanical strength and stimuli-free SELF properties to the hydrogel via dynamic catecholato-metal coordination bonds. Additionally, the catechol groups of TA provide mussel-inspired adhesion properties to the hydrogel. Due to its electroconductivity, toughness, stimuli-free SELF properties, and self-adhesiveness, a prototype soft wearable strain sensor is created using this hydrogel and subsequently tested.

scholarly journals High-strength and fibrous capsule–resistant zwitterionic elastomers

2021 ◽  
Vol 7 (1) ◽  
pp. eabc5442
Author(s):  
Dianyu Dong ◽  
Caroline Tsao ◽  
Hsiang-Chieh Hung ◽  
Fanglian Yao ◽  
Chenjue Tang ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Mechanical Strength ◽  
High Strength ◽  
Design Principles ◽  
Fibrous Capsule ◽  
High Mechanical Strength ◽  
Capsule Formation ◽  
Locking Mechanism ◽  
Fibrous Capsule Formation

The high mechanical strength and long-term resistance to the fibrous capsule formation are two major challenges for implantable materials. Unfortunately, these two distinct properties do not come together and instead compromise each other. Here, we report a unique class of materials by integrating two weak zwitterionic hydrogels into an elastomer-like high-strength pure zwitterionic hydrogel via a “swelling” and “locking” mechanism. These zwitterionic-elastomeric-networked (ZEN) hydrogels are further shown to efficaciously resist the fibrous capsule formation upon implantation in mice for up to 1 year. Such materials with both high mechanical properties and long-term fibrous capsule resistance have never been achieved before. This work not only demonstrates a class of durable and fibrous capsule–resistant materials but also provides design principles for zwitterionic elastomeric hydrogels.

scholarly journals Recyclable Self-Healing Polyurethane Cross-Linked by Alkyl Diselenide with Enhanced Mechanical Properties

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 773 ◽  
Author(s):  
Yuqing Qian ◽  
Xiaowei An ◽  
Xiaofei Huang ◽  
Xiangqiang Pan ◽  
Jian Zhu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Room Temperature ◽  
Amide Bond ◽  
Self Healing ◽  
Healing Efficiency ◽  
Polyurethane Networks ◽  
Combined Action ◽  
Cross Linker ◽  
Dynamic Structures ◽  
External Interventions

Dynamic structures containing polymers can behave as thermosets at room temperature while maintaining good mechanical properties, showing good reprocessability, repairability, and recyclability. In this work, alkyl diselenide is effectively used as a dynamic cross-linker for the design of self-healing poly(urea–urethane) elastomers, which show quantitative healing efficiency at room temperature, without the need for any catalysts or external interventions. Due to the combined action of the urea bond and amide bond, the material has better mechanical properties. We also compared the self-healing effect of alkyl diselenide-based polyurethanes and alkyl disulfide-based polyurethanes. The alkyl diselenide has been incorporated into polyurethane networks using a para-substituted amine diphenyl alkyl diselenide. The resulting materials not only exhibit faster self-healing properties than the corresponding disulfide-based materials, but also show the ability to be processed at temperatures as low as 60 °C.

scholarly journals Room-temperature autonomous self-healing glassy polymers with hyperbranched structure

2020 ◽  
Vol 117 (21) ◽  
pp. 11299-11305 ◽  
Author(s):  
Hao Wang ◽  
Hanchao Liu ◽  
Zhenxing Cao ◽  
Weihang Li ◽  
Xin Huang ◽  
...  
Keyword(s):  
Hydrogen Bonds ◽  
Room Temperature ◽  
Glassy State ◽  
Glassy Polymers ◽  
Self Healing ◽  
External Branch ◽  
Healing Efficiency ◽  
High Degree ◽  
External Stimuli ◽  
Hyperbranched Structure

Glassy polymers are extremely difficult to self-heal below their glass transition temperature (Tg) due to the frozen molecules. Here, we fabricate a series of randomly hyperbranched polymers (RHP) with high density of multiple hydrogen bonds, which showTgup to 49 °C and storage modulus up to 2.7 GPa. We reveal that the hyperbranched structure not only allows the external branch units and terminals of the molecules to have a high degree of mobility in the glassy state, but also leads to the coexistence of “free” and associated complementary moieties of hydrogen bonds. The free complementary moieties can exchange with the associated hydrogen bonds, enabling network reconfiguration in the glassy polymer. As a result, the RHP shows amazing instantaneous self-healing with recovered tensile strength up to 5.5 MPa within 1 min, and the self-healing efficiency increases with contacting time at room temperature without the intervention of external stimuli.

scholarly journals A Self-Healing Polymer with Fast Elastic Recovery upon Stretching

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 597 ◽  
Author(s):  
Pei-Chen Zhao ◽  
Wen Li ◽  
Wei Huang ◽  
Cheng-Hui Li
Keyword(s):  
Room Temperature ◽  
Elastic Recovery ◽  
Self Healing ◽  
Original Length ◽  
Healing Efficiency ◽  
Recovery Behavior ◽  
Long Time ◽  
Highly Stretchable ◽  
Soft Actuators

The design of polymers that exhibit both good elasticity and self-healing properties is a highly challenging task. In spite of this, the literature reports highly stretchable self-healing polymers, but most of them exhibit slow elastic recovery behavior, i.e., they can only recover to their original length upon relaxation for a long time after stretching. Herein, a self-healing polymer with a fast elastic recovery property is demonstrated. We used 4-[tris(4-formylphenyl)methyl]benzaldehyde (TFPM) as a tetratopic linker to crosslink a poly(dimethylsiloxane) backbone, and obtained a self-healing polymer with high stretchability and fast elastic recovery upon stretching. The strain at break of the as-prepared polymer is observed at about 1400%. The polymer can immediately recover to its original length after being stretched. The damaged sample can be healed at room temperature with a healing efficiency up to 93% within 1 h. Such a polymer can be used for various applications, such as functioning as substrates or matrixes in soft actuators, electronic skins, biochips, and biosensors with prolonged lifetimes.

Self-healable gradient copolymers

2019 ◽  
Vol 3 (3) ◽  
pp. 464-471 ◽  
Author(s):  
Jing Cui ◽  
Zhe Ma ◽  
Li Pan ◽  
Chun-Hua An ◽  
Jing Liu ◽  
...  
Keyword(s):  
Mechanical Strength ◽  
Ionic Interactions ◽  
Self Healing ◽  
Gradient Copolymers ◽  
High Mechanical Strength ◽  
Gradient Distribution

Synergistic hard/soft gradient distribution and dynamic ionic interactions impart high mechanical strength, toughness, stretchability and tenacious self-healing ability to copolymers.

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