Progress in devulcanization of waste tire rubber: Upcycling towards a circular economy
Zaheer ul Haq
, Teng Ren, Xinyan Yue, Krzysztof Formela
, Denis Rodrigue
, Xavier Colom Fajula
, Tony McNally
, Dong Dawei, Yong Zhang
, Shifeng Wang
, Teng Ren, Xinyan Yue, Krzysztof Formela
, Denis Rodrigue
, Xavier Colom Fajula
, Tony McNally
, Dong Dawei, Yong Zhang
, Shifeng Wang
Vol. 19., No.3., Pages 258-293, 2025
DOI: 10.3144/expresspolymlett.2025.20
DOI: 10.3144/expresspolymlett.2025.20
GRAPHICAL ABSTRACT

ABSTRACT
As a complex composite material, tire rubber has always presented significant environmental and waste management concerns due to its non-biodegradability and accumulation in landfills. The devulcanization of tire rubber has emerged as a historical challenge in the field of sustainable rubber engineering since Goodyear invented cross-linking in 1839. This review provides a comprehensive analysis of waste tire recycling processes, focusing on the sources, legislation, management strategies, and utilization across different regions. It explores the multifaceted challenges of devulcanizing rubber, with a specific focus on transitioning from ground tire rubber to the concept of multi-decrosslinking: sulfur bridge breakage, rubber chain depolymerization and micro-nano sized core-shell carbon black. Ideal devulcanization has restricted the release of reinforcing fillers, resulting in devulcanized rubber mainly containing dozens of micron particles, which hinder the wide usage of devulcanized rubber. This review comprehensively assesses the current state-of-the-art techniques for tire rubber devulcanization, including physical, chemical and biological methods. It explores the intricacies of ground tire rubber as a starting material, structural evolution of ground tire rubber during the devulcanization process and the associated challenges in achieving efficient devulcanization while retaining desirable mechanical properties. Furthermore, through an in-depth analysis of recent advancements, limitations and prospects, this paper offers a complete understanding of the challenges faced in tire rubber devulcanization. Considering the technical and environmental aspects of these processes, this work contributes to multi-decrosslinking, the ongoing discourse on sustainable materials development and circular economy initiatives, which pave the way for future innovations in the field of rubber recycling.
RELATED ARTICLES
Bokome Shaku, Reagan L. Mohlala, Kabelo B. Dilebo, Tshwafo E. Motaung
Vol. 20., No.9., Pages 905-922, 2026
DOI: 10.3144/expresspolymlett.2026.67
Vol. 20., No.9., Pages 905-922, 2026
DOI: 10.3144/expresspolymlett.2026.67

Cigarette butts (CBs) are among the most abundant forms of anthropogenic litter worldwide and constitute a persistent source of environmental contamination due to their slow degradation and the release of toxic substances into terrestrial and aquatic ecosystems. This review critically evaluates recent advances in the valorisation of CB waste into value-added functional materials. Particular attention is given to conversion strategies including chemical activation, electrospinning, hydrothermal processing, and nanocomposite fabrication. These approaches enable the production of activated carbons, cellulose-derived nanomaterials, and metal-doped composites with promising applications in water purification, energy storage, vector control, and pollutant remediation. The underlying mechanisms, performance, scalability, and sustainability of these technologies are discussed. Finally, current challenges, research gaps, and future opportunities of large-scale implementation are highlighted. Collectively, the findings demonstrate that CBs can be re-envisioned not only as a persistent environmental pollutant but also as valuable secondary resources that support circular economy and sustainable material development strategies.
Andrea Kohári, Tamás Bárány
Vol. 20., No.9., Pages 923-938, 2026
DOI: 10.3144/expresspolymlett.2026.68
Vol. 20., No.9., Pages 923-938, 2026
DOI: 10.3144/expresspolymlett.2026.68

The virgin polymer content of thermoplastic polyurethane (TPU) can be reduced with the use of recycled tire rubber, but blend properties strongly depend on the structure of the rubber phase. In this study, we compared TPU-based compounds containing ground tire rubber (GTR), devulcanized GTR (dGTR) and dynamically revulcanized dGTR in terms of mechanical and rheological behavior. GTR-filled blends showed higher tensile strength at the same rubber content, whereas dGTR-containing blends exhibited higher elongation at break up to 40 wt% rubber. Among the thermoplastic dynamic vulcanizates, peroxide-cured blends provided higher tensile strength, higher elongation at break and lower compression set than sulfur-cured blends. The rubber phase also strongly affected melt rheology: dGTR-containing blends showed higher storage modulus (G′) and complex viscosity (η*) than the corresponding GTR-filled blends over the entire frequency range. In contrast, there were only minor rheological differences between sulfur- and peroxide-cured systems, indicating that rubber content had a stronger effect on melt behavior than the curing system. The novelty of this study is the direct comparison of GTR, dGTR and dynamically revulcanized dGTR within the same TPU matrix, showing how the breakdown and partial rebuilding of the recycled rubber network can be used to tune both solid-state properties and melt processability in TPU compounds with high recycled content.
Xavier Colom, Scott Martínez, Fernando Carrillo-Naverrete, Javier Cañavate
Vol. 20., No.2., Pages 114-126, 2026
DOI: 10.3144/expresspolymlett.2026.10
Vol. 20., No.2., Pages 114-126, 2026
DOI: 10.3144/expresspolymlett.2026.10

The need to recycle elastomeric waste requires studying its viability in industrial applications. This study investigates the feasibility of recycling elastomeric waste by analyzing whether virgin ethylene-propylene-diene monomer (EPDM) can be replaced by blends of virgin EPDM and thermomechanically and microwave devulcanized EPDM (EPDMd) in industrial applications from the perspective of environmental degradation. Two types of samples were examined: conventional EPDM used to roof membranes, and EPDM blended with different amounts (20, 40, and 50 phr) of EPDMd. Samples were subjected to natural aging in coastal and mountainous environments. Results show that mechanical properties decline with higher EPDMd content and, to a lesser degree, with prolonged outdoor exposure. The coastal climate proved more aggressive than the mountainous one when EPDMd content exceeded 40 phr. Zinc stearate (ZnSt2), a byproduct of vulcanization, was found to influence the evolution of the mechanical behavior. The combined analysis of scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), abrasion tests, and thermogravimetric analysis (TGA) provided insights into the degradation processes of these elastomeric blends.
Longqiang Xiao, Weijia Huang, Kaihong Lin, Shucui Han, Zuyun Luo, Linxi Hou, Yan’gen LV
Vol. 20., No.1., Pages 3-17, 2026
DOI: 10.3144/expresspolymlett.2026.2
Vol. 20., No.1., Pages 3-17, 2026
DOI: 10.3144/expresspolymlett.2026.2

In this study, magnetic core-shell Fe3O4@ZIF-8 was synthesized via a hydrothermal method and applied to Polyethylene terephthalate(PET) degradation. The catalytic degradation of PET by Fe3O4@ZIF-8 was carried out under atmospheric pressure, yielding high-value bis(2-hydroxyethyl) terephthalate (BHET) monomers. The as-synthesized Fe3O4@ZIF-8 core-shell composites possess hierarchical porosity with tunable nanoscale cavities. SEM and TEM analyses confirmed the core-shell morphology, with nanoparticles having a size distribution of 180–280 nm. The degradation product was identified as a high-purity, colorless, and transparent monomeric BHET through 1H NMR and LC analyses. Based on a series of onefactor experiments and a Box-Behnken experimental design, the optimal process conditions were determined to be an alcoholysis temperature of 200°C, a catalyst dosage of 0.5 wt% (relative to PET mass), a reaction time of 50 min, and an ethylene glycol-to-PET mass ratio of 4.5:1. Under these conditions, the actual BHET yield reached 81.12%, closely matching the predicted value.
Katalin Bocz, Ferenc Ronkay
Vol. 19., No.9., Pages 860-861, 2025
DOI: 10.3144/expresspolymlett.2025.65
Vol. 19., No.9., Pages 860-861, 2025
DOI: 10.3144/expresspolymlett.2025.65

This is an editorial article. It has no abstract.



