WAITING
Search for articles
search


Research article
|
|
A comparison of the mechanical behaviour of natural rubber-based blends using waste rubber particles obtained by cryogrinding and high-shear mixing
Nicolas Candau, Rachel LeBlanc, Maria Lluisa Maspoch
Vol. 17., No.11., Pages 1135-1153, 2023
DOI: 10.3144/expresspolymlett.2023.86
Corresponding author: Nicolas Candau

GRAPHICAL ABSTRACT

ABSTRACT

The influence of the type of mechanical recycling of waste rubber particles on the tensile properties of waste/natural rubber blends has been investigated. The wastes originating from ground tyre rubber (GTR) had been treated by two distinct processes: cryo-grinding and high shear mixing (HSM). For both processes, the resulting composites show enhanced stiffness and strength for all strain rates and temperatures tested. This is attributed to both the reinforcing effect of the waste as well as the nucleation ability of the wastes on strain induced crystallization (SIC) in the natural rubber (NR) matrix. Cryo-grinding was shown to provide the finest particle size with an average diameter of 34 μm, while the HSM process was found to show an elastic modulus of aggregated GTR powder of 7 MPa at 1 Hz at room temperature. Within these characteristics, the NR/GTR blends using the HSM process show the best tensile performance under single loading, with the highest strength and highest ability to crystallize under strain. Under cyclic loading, NR/GTR blends using cryo-ground GTR particles show the best performance, which we ascribed to their ability to better distribute and accommodate the stress from one cycle to another owing to their finest size. Both explored recycling techniques provide the natural/waste rubber blends interesting properties such as mechanical reinforcement and strain-induced crystallization ability under various testing conditions.


RELATED ARTICLES

Is it possible to utilize rejected natural rubber gloves as matrix for rubber composites?
Nabil Hayeemasae, Siriwat Soontaranon, Abdulhakim Masa
Vol. 20., No.7., Pages 664-676, 2026
DOI: 10.3144/expresspolymlett.2026.50
We investigated the possibility of applying rejected natural rubber gloves (RNRGs) as a matrix for rubber composites filled with sepiolite. The virgin natural rubber (NR) samples were also prepared for comparison. Clearly, the RNRGs can be re-mixed with rubber chemicals, re-shaped, and revulcanized. Maximum torque increased with sepiolite loading during vulcanization, along with stress at 100 and 300% strains and strain-induced crystallization ability, whereas the tensile strength and elongation at break of the RNRG composites exhibited an opposite trend. The unfilled RNRG possessed high tensile strength (~19.86 MPa) and extensibility (~600%), which was about 67% higher than that of the unfilled NR sample. However, increased sepiolite loading decreased the thermomechanical properties of the RNRG composites because the RNRG had undergone vulcanization before re-mixing and revulcanizing; the NR-based composite showed the opposite trend. Based on the results, the RNRGs can be re-used as the rubber matrix of rubber compounds when thermal properties are not critical.
Sustainability in the rubber industry: State of the art
Péter Tamás-Bényei, Andrea Kohári, Ákos Görbe, Lóránt Kiss, Katalin Litauszki, Ferenc Szabó, László Mészáros, Károly Renner, Tamás Bárány
Vol. 20., No.6., Pages 547-550, 2026
DOI: 10.3144/expresspolymlett.2026.41
This is an editorial article. It has no abstract.
Rheological stability as the missing criterion in HDPE circularity: A critical review and a new decision framework
Maja Csapó, József Gábor Kovács
Vol. 20., No.4., Pages 414-434, 2026
DOI: 10.3144/expresspolymlett.2026.32
The greatest obstacle to recycling post-consumer high-density polyethylene (PCR-HDPE) is typically the degradation of properties caused by impurities and heterogeneity. However, a critical analysis of the literature reveals that the real bottleneck is not the material composition, but rather rheological stability, which simultaneously determines the degradation history of the waste stream, melt behavior, and processability at the cycle level. This review proposes a new perspective: the decision among mechanical, chemical, and energetic recycling is better made based on a unified rheological stability index (RSI), which integrates carbonyl index, viscosity change after multiple instances of melting, melt flow index (MFI) instability, in-mold pressure fluctuation, and the degree of polymer incompatibility. RSI enables the prediction of the processability of PCR-HDPE and identifies which recycling path a fraction is most suitable for. The study demonstrates how an RSI-based approach can reduce quality risk, improve cycle stability, and support circular decision-making in an industrial environment.
Reinforcing effect of thermo-oxidative reclaimed rubber on NR/SBR blends for tire tread applications
Yunhui Xu, Zaheer ul Haq, Junrong Li, Hui Tu, Zaixue Wang, Houluo Cong
Vol. 20., No.2., Pages 142-153, 2026
DOI: 10.3144/expresspolymlett.2026.12
This study explores the application of thermo-oxidative reclaimed ground tire rubber (RGTR) in natural rubber (NR)/styrene butadiene rubber (SBR) composite, focusing on its impact on morphology, mechanical properties, rheological behavior, vulcanization characteristics, aging resistance, tear strength and abrasion resistance. The findings revealed that RGTR enhances the tear strength and abrasion resistance of NR/SBR composites while maintaining comparable tensile strength, elongation at break, and modulus. The incorporation of RGTR reduced Mooney viscosity of the NR/SBR composites and improved flowability. It also shortened the vulcanization time and enhanced vulcanization efficiency. The NR/SBR composites with RGTR loadings below 60 phr exhibited optimal performance, achieved a maximum tear strength of 93.77 N/mm and improved abrasion resistance. However, higher RGTR content led to increased agglomeration, as evidenced by scanning electron microscopy (SEM), which showed finer dispersion at lower RGTR contents and larger aggregates at higher loadings. These findings demonstrate the potential of RGTR as a sustainable additive for enhancing specific properties in NR/SBR composites, contributing to both performance optimization and waste tire management.
Developing thermo-remoldable blends by combining natural rubber bearing benzyl chloride groups with gelatin
Rattanawadee Ninjan, Bencha Thongnuanchan, Phakawat Tongnuanchan, Subhan Salaeh, Jutharat Intapun, Abdulhakim Masa, Natinee Lopattananon
Vol. 20., No.1., Pages 18-35, 2026
DOI: 10.3144/expresspolymlett.2026.3
The present study has proposed a straightforward method to improve the reprocessability of modified natural rubber (NR) by blending it with gelatin (GT). The reprocessable characteristics of these blends were evaluated based on their remolding capabilities and mechanical recovery performance. In this method, poly(vinylbenzyl chloride) (PVBC) was first grafted onto NR chains to create graft copolymers known as NR-g-PVBC. The benzyl chloride groups in the graft copolymers were subsequently converted into quaternary ammonium groups, referred to as NR-g-QPVBC. This modification enabled ionic crosslinking when NR-g-QPVBC reacted with ethylenediamine tetraacetic acid. Blends were created by incorporating GT powder into the NR-g-QPVBC latex. The optimal loading level of GT was determined to be 30 wt%, as the resulting film exhibited the highest recovery of tensile properties. Initially, the film's tensile strength was measured at 15 MPa. After being remolded at 160 °C, the tensile strength decreased to 9.3 MPa, resulting in a recovery rate of 60.7% and withstanding a tensile strain of 144%. Although the NR-g-QPVBC/GT films could be remolded, their tensile properties declined with increasing remolding cycles. Therefore, this work demonstrated a practical method for producing NR-based films that could be reshaped through hot-pressing after being formed into products, increasing their reusability.
Published by:

Budapest University of Technology and Economics,
Faculty of Mechanical Engineering, Department of Polymer Engineering