Electron beam (EB) treatment of a high vinyl styrene-butadiene-styrene (SBS) block copolymer was accomplished by exposing the polymer to high-energy electrons generated from an electron accelerator. This resulted in the formation of free radicals of carbon on the polybutadiene units in the backbone of the elastomer and subsequent radical coupling to produce cross-links. In the process, some unavoidable chain scission (CS) also occurred. An attempt was made to mathematically trace the nature of the CS as a function of radiation dose with the aid of the experimentally determined cross-link density (CLD), tensile strength and tear strength, the latter three also obtained as functions of radiation dose. The radiation dose was varied from 12.5 to 300.0 kGy in multiples of 12.5 kGy. The novelty of the work was, in part to create a function that can be used to calculate chain-scission in dependence of EB radiation dose. It was found that a change in the ratio of CS to CLD occurred as a function of radiation dose over the previously calculated constant ratio, using the Charlesby-Pinner equation.

Analyzing rubber waste is crucial for value-added recycling, but the multitude of ingredients in vulcanized networks makes it challenging to characterize cross-linked rubbers. A combination of analytical techniques is usually required. In this study, two complementary characterization techniques, based on Fourier transform infrared (FTIR) spectroscopy and derivative thermogravimetric analysis (DTGA) were applied to analyze the structural, physical, and thermal behavior of ground tire rubber (GTR) samples devulcanized by two different processes. A set of samples was devulcanized by only microwaves (MW) while another set was treated with a combination of a thermochemomechanical (TM) process, which included the use of a devulcanization aid such as benzoyl peroxide, and microwaves. The combined technique proved to be more efficient in terms of the degree of devulcanization, significantly reducing the cross-linking density. However, the combined thermochemomechanical and microwave (TM/MW) devulcanization process resulted in greater degradation of the main rubber chains in the cross-linked network compared to the process using only microwaves.

Silicone rubber magnetorheological elastomers (SR-MREs) are increasingly recognized for their resilience in marine conditions, offering prolonged service life and durability. This study evaluates the one-month durability of silicone rubber magnetorheological elastomers (SR-MREs) under seawater conditions. Results revealed a 6% reduction in hardness and an 8% decrease in Young’s modulus compared to unimmersed samples. Morphological and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) analyses supported these findings, revealing surface defects and chemical bonding changes. The immersed SR-MRE displayed a notable 250% increase in elongation at break, highlighting enhanced elasticity. Rheological properties revealed complex mechanical behavior, with an initial increase in storage modulus from 0.25 to 0.38 MPa in the presence of a magnetic field, followed by a gradual decrease to 0.15 MPa at 0 A and 0.52 Mpa at 5 A with strain. Additionally, this study proposes an illustrative mechanism to elucidate the relationship between seawater elements and SR-MRE behavior, enhancing our understanding of its mechanical properties and degradation in marine environments, thus highlighting SR-MRE’s potential as a durable material compared to traditional rubber composites.

The global concern over zinc leaching into aquatic ecosystems has led researchers to seek ways to reduce zinc oxide (ZnO) content in rubber products. Conventional microsized ZnO, commonly used in the rubber industry, poses dispersion challenges due to its hydrophilic nature and micron size within the hydrophobic rubber matrix. Therefore, higher amounts of ZnO are added, elevating the risk to aquatic life. A promising alternative involves using highly dispersible ZnO with active zinc (Zn) centers instead of conventional ZnO. Another approach includes incorporating ZnO-anchored silica particles into the rubber matrix, which requires additional ex-situ fabrication. This study presents an innovative method where ZnO-anchored silica is generated in situ during the blending of styrene-butadiene rubber/natural rubber (SBR/NR). The study also evaluates the effectiveness of active, nano-sized, and octylamine-modified ZnO as activators compared to conventional ZnO, by introducing silica filler, octylamine-modified and high surface area ZnO anchor onto the silica surface, forming Si–O–Zn covalent bonds. This protective layer reduces filler aggregation and the Payne effect. Even with 60% less usage, these activators in the SBR/NR blend significantly enhance tensile strength (31.27%) and elongation at break (49.13%) compared to conventional ZnO. These results point towards the possibility of a cost-effective and sustainable replacement for conventional ZnO.

Conductive carbon black (CCB), carbon nanotubes (CNT) and its hybrids are introduced into the natural rubber (NR) matrix aiming to explore the effect of filler ratio on the transport properties. Solvent transport of NR is found to decrease for hybrid filler systems as compared to single filler incorporated systems. Kinetic parameters of solvent transport behavior of filled NR systems are analyzed using various kinetic models. Upon the computation of kinetic parameters of transport data, it is found that the Peppas-Sahlin model is in good agreement with experimental observations, which suggests that the transport mechanism is diffusion controlled. Rubber–filler interaction parameters are computed and analyzed from the swelling experiments using Kraus, Cunneen-Russel, and Lorenz-Park equations