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Harvard researchers develop tough, self-healing rubber

Researchers from the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS) have developed a new type of rubber that is as tough as natural rubber but can also self-heal. The research is published in Advanced Materials.

Self-healing materials aren’t new—researchers at SEAS have developed self-healing hydrogels, which rely on water to incorporate reversible bonds that can promote healing. However, engineering self-healing properties in dry materials such as rubber has proven more challenging. Rubber is made of polymers often connected by permanent, covalent bonds. While these bonds are incredibly strong, they will never reconnect once broken. In order to make a rubber self-healable, the team needed to make the bonds connecting the polymers reversible, so that the bonds could break and reform.

Previous research used reversible hydrogen bonds to connect polymers to form a rubber but reversible bonds are intrinsically weaker than covalent bonds. This raised the question, can we make something tough but can still self-heal?

—Li-Heng Cai, a postdoctoral fellow at SEAS and corresponding author

Cai, along with Jinrong Wu, a visiting professor from Sichuan University, China, and senior author David A. Weitz, Mallinckrodt Professor of Physics and Applied Physics, developed a hybrid rubber with both covalent and reversible bonds.

The concept of mixing both covalent and reversible bonds to make a tough, self-healing rubber was proposed in theory by Cai but never shown experimentally because covalent and reversible bonds don’t like to mix. These two types of bonds are intrinsically immiscible, like oil and water, said Cai.

The researchers developed a molecular rope to tie these two types of bonds together. This rope, called randomly branched polymers, allows two previously unmixable bonds to be mixed homogeneously on a molecular scale. In doing so, they were able to create a transparent, tough, self-healing rubber.

The randomly branched polymer links such two types of bonds and forces them to mix on the molecular level without cosolvents. This enables a hybrid “dry” elastomer that is very tough with fracture energy 13500 Jm−2 comparable to that of natural rubber. Moreover, the elastomer can self-heal at room temperature with a recovered tensile strength 4 MPa, which is 30% of its original value, yet comparable to the pristine strength of existing self-healing polymers.

—Wu et al.

Typical rubber tends to crack at certain stress point when force is applied. When stretched, hybrid rubber develops so-called crazes throughout the material, a feature similar to cracks but connected by fibrous strands. These crazes redistribute the stress, so there is no localized point of stress that can cause catastrophic failure. When the stress is released, the material snaps back to its original form and the crazes heal.

Harvard’s Office of Technology Development has filed a patent application for the technology and is actively seeking commercialization opportunities. The self-healing ability is appealing for a wide variety of rubber products.

There is still a lot more to do,. For materials science, it is not fully understood why this hybrid rubber exhibits crazes when stretched. For engineering, the applications of the hybrid rubber that take advantage of its exceptional combination of optical transparency, toughness, and self-healing ability remain to be explored. Moreover, the concept of using molecular design to mix covalent and reversible bonds to create a homogenous hybrid elastomer is quite general and should enable development of tough, self-healing polymers of practical usage.

—David A. Weitz

The research was supported by the National Science Foundation, Harvard Materials Research Science and Engineering Center (MRSEC) and the National Institute of Health/National Heart, Lung and Blood Institute.

Resources

  • J. Wu, L.-H. Cai, D. A. Weitz (2017) “Tough Self-Healing Elastomers by Molecular Enforced Integration of Covalent and Reversible Networks” Adv. Mater. doi: 10.1002/adma.201702616

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