Every year, millions of tires end up in landfills, creating an environmental crisis with far-reaching consequences. In the United States alone, over 274 million tires were scrapped in 2021, with nearly 20% of them being discarded in landfills. The accumulation of these waste materials presents not only a space issue but also introduces environmental hazards, such as chemical leaching and spontaneous combustion.

While pyrolysis—a process that chemically recycles rubber through high-temperature decomposition—is widely used, it generates harmful byproducts like benzene and dioxins, posing health and environmental risks.

A study titled “Deconstruction of Rubber via C–H Amination and Aza-Cope Rearrangement,” published in Nature, introduces a novel chemical method for breaking down rubber waste. This technique utilizes C–H amination and a polymer rearrangement strategy to transform discarded rubber into valuable precursors for epoxy resins, offering an innovative and sustainable alternative to traditional recycling methods.

The research was led by Dr. Aleksandr Zhukhovitskiy, William R. Kenan, Jr. Fellow and Assistant Professor in the Department of Chemistry at UNC-Chapel Hill.

Rubber, including the synthetic kind used in tires, is composed of polymers cross-linked together into a three-dimensional network that behaves as a tough, flexible material. Recycling these materials is difficult due to the extensive cross-linking within the polymer structure, which gives rubber its durability but also makes it resistant to degradation.

Traditional methods for breaking down rubber focus on two main approaches: devulcanization, which breaks sulfur cross-links but weakens the polymer’s mechanical properties; and cleavage of the polymer backbones using oxidative or catalytic methods, which often results in complex, low-value byproducts. Neither approach provides an efficient, scalable solution for repurposing rubber waste.

“Our research seeks to overcome these challenges by developing a method that breaks down rubber into functional materials that possess value even as a mixture,” said Dr. Zhukhovitskiy, who is the corresponding author of the study.

The researchers introduced a sulfur diimide reagent to enable the installation of amine groups at specific locations in the polymer chains. This step is crucial because it sets the stage for the subsequent backbone rearrangement. This chemical reaction reorganizes the polymer backbone, breaking down the rubber into soluble amine-functionalized materials that can be used to produce epoxy resins.

The researchers showed that their two-step process works very well. In a test with a model polymer, they broke it down significantly, reducing its molecular weight from 58,100 g/mol to about 400 g/mol. When they applied the method to used rubber, it broke down completely in just six hours, turning it into a soluble material with amine groups that could be used to manufacture broadly useful materials like epoxy resins.

The efficiency of this method is particularly striking when compared to traditional recycling techniques, which often require extreme temperatures or expensive catalysts. The researchers achieved their results under mild conditions (35–50°C, or 95–122°F) in aqueous media, making the process more environmentally friendly and cost-effective.

Epoxy resins are widely used in industries for adhesives, coatings, and composites. They are usually made from petroleum-based chemicals like bisphenol A and curing agents. This research shows that amine-modified poly-dienes, produced using the researchers’ method, can create epoxy materials with strengths similar to commercial resins.

“In moments like this, I come to appreciate the power of organic synthesis,” said Maxim Ratushnyy, a co-author of the paper and former postdoctoral scholar at UNC-Chapel Hill. “It is fascinating to see the ease with which the developed sequence of simple, yet powerful, organic transformations can take on a stubborn C–C bond and convert polybutadiene and polyisoprene-based rubbers into potentially valuable epoxy resins.”

Beyond its practical applications, this study marks a significant step toward greener recycling technologies. The researchers evaluated the environmental impact of their process using the Environmental Impact Factor (E-factor), a measure of waste generated relative to the product yield.

“E-factor is a simple but powerful metric to compare the impact of a new process to incumbents, and also to highlight process steps that can be improved as we work to transition this process out of the lab and into practice,” said Dr. Geoff Lewis, a research specialist at the University of Michigan’s Center for Sustainable Systems.

While the complete E-factor, which includes solvent use, was high, the simple E-factor, excluding solvents, was much lower, highlighting areas where the process could be further optimized for sustainability. The team is already exploring greener solvent systems and alternative reaction conditions to reduce waste generation.

“Our research represents a paradigm shift in how we approach the problem of rubber waste,” said Sydney Towell, a co-author of the study and Ph.D. candidate at UNC-Chapel Hill.

“By harnessing the power of C–H amination and backbone rearrangement, this method provides a new pathway to transforming post-consumer rubber into high-value materials, reducing reliance on landfills and minimizing environmental harm.”