Effects of shear stress and subcritical water on devulcanization of styrene-butadiene rubber based ground tire rubber in a twin-screw extruder

2013 ◽  
Vol 130 (3) ◽  
pp. 1845-1854 ◽  
Author(s):  
Xiaojun Wang ◽  
Changping Shi ◽  
Ling Zhang ◽  
Yuncan Zhang
Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1139
Author(s):  
Hans van Hoek ◽  
Jacques Noordermeer ◽  
Geert Heideman ◽  
Anke Blume ◽  
Wilma Dierkes

De-vulcanization of rubber has been shown to be a viable process to reuse this valuable material. The purpose of the de-vulcanization is to release the crosslinked nature of the highly elastic tire rubber granulate. For present day passenger car tires containing the synthetic rubbers Styrene-Butadiene Rubber (SBR) and Butadiene Rubber (BR) and a high amount of silica as reinforcing filler, producing high quality devulcanizate is a major challenge. In previous research a thermo-chemical mechanical approach was developed, using a twin-screw extruder and diphenyldisulfide (DPDS) as de-vulcanization agent.The screw configuration was designed for low shear in order to protect the polymers from chain scission, or uncontrolled spontaneuous recombination which is the largest problem involved in de-vulcanization of passenger car tire rubber. Because of disadvantages of DPDS for commercial use, 2-2′-dibenzamidodiphenyldisulfide (DBD) was used in the present study. Due to its high melting point of 140 °C the twin-screw extruder process needed to be redesigned. Subsequent milling of the devulcanizate at 60 °C with a narrow gap-width between the mill rolls greatly improved the quality of the devulcanizate in terms of coherence and tensile properties after renewed vulcanization. As the composition of passenger car tire granulate is very complex, the usefulness of the Horikx-Verbruggen analysis as optimization parameter for the de-vulcanization process was limited. Instead, stress-strain properties of re-vulcanized de-vulcanizates were used. The capacity of the twin-screw extruder was limited by the required residence time, implying a low screw speed. A best tensile strength of 8 MPa at a strain at break of 160% of the unblended renewed vulcanizate was found under optimal conditions.


2014 ◽  
Vol 34 (6) ◽  
pp. 543-554 ◽  
Author(s):  
Fazliye Karabork ◽  
Erol Pehlivan ◽  
Ahmet Akdemir

Abstract Ground tire rubber (GTR) was devulcanized by microwaves at the same heating rate (constant power) and different times of exposure. The devulcanized rubber (DV-R) and untreated GTR were characterized physically and thermally. Composite materials were prepared from different proportions of the GTR, which was used as a filler, and the DV-R, which was used as part of the styrene butadiene rubber (SBR) matrix, and by varying the exposure time of the microwave power. These composites were compared with a control sample that was prepared from virgin SBR. The sol content (soluble part) and Fourier transform infrared spectroscopy (FTIR) analyses of the devulcanized samples were examined to define the efficiency of devulcanization. The cure characteristics and tensile properties of the SBR composites were researched. In this study, it was found that using DV-R as part of the rubber matrix produced much better properties than using GTR as a filler, thereby showing the significant benefits of microwave devulcanization. At the DV-R content of 50 phr, the elongation at break of the DV-R 5 min/SBR composites increased to 445.06% from 217.25% for the GTR/SBR composites, i.e., the elongation at break was enhanced by 105% by the devulcanization of GTR. Scanning electron microscopy (SEM) photographs displayed a better interface coherence between the DV-R 5 min and SBR matrix than the GTR/SBR composites.


2021 ◽  
Vol 4 (2) ◽  
pp. 103-108
Author(s):  
Pirityi Dávid Zoltán ◽  
Pölöskei Kornél

Abstract The environmental impact of rubber waste can be reduced by extending the lifetime of rubber products. It can be achieved by developing graphene/rubber nanocomposites with good abrasion resistance. In this paper, we investigated how rubber mixing technologies influence the mechanical properties of rubber. We added various amounts (0, 1, 5 and 10 phr) of graphite and graphene to rubber mixtures using a two-roll mill, an internal mixer, a single- and a twin-screw extruder. We performed tensile, tear strength and Shore A hardness tests on the vulcanisates and analysed their fracture surfaces with a scanning electron microscope. Our results show that graphene had a better reinforcing effect than graphite. Rubber mixing via extrusion may contribute to more severe polymer degradation, though their reproducibility is better than that achieved on a two-roll mill or in an internal mixer.


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