Effect of low molecular weight polybutadiene as processing aid on properties of silica-filled styrene-butadiene rubber compounds

2003 ◽  
Vol 90 (11) ◽  
pp. 3135-3140 ◽  
Author(s):  
Sung-Seen Choi ◽  
Byung-Ho Park ◽  
Changwoon Nah
Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1626
Author(s):  
Abdullah Gunaydin ◽  
Clément Mugemana ◽  
Patrick Grysan ◽  
Carlos Eloy Federico ◽  
Reiner Dieden ◽  
...  

A set of poly(isobornyl methacrylate)s (PIBOMA) having molar mass in the range of 26,000–283,000 g mol−1 was prepared either via RAFT process or using free radical polymerization. These linear polymers demonstrated high glass transition temperatures (Tg up to 201 °C) and thermal stability (Tonset up to 230 °C). They were further applied as reinforcing agents in the preparation of the vulcanized rubber compositions based on poly(styrene butadiene rubber) (SBR). The influence of the PIBOMA content and molar mass on the cure characteristics, rheological and mechanical properties of rubber compounds were studied in detail. Moving die rheometry revealed that all rubber compounds filled with PIBOMA demonstrated higher torque increase values ΔS in comparison with rubber compositions without filler, independent of PIBOMA content or molar mass, thus confirming its reinforcing effect. Reinforcement via PIBOMA addition was also observed for vulcanized rubbers in the viscoelastic region and the rubbery plateau, i.e. from −20 to 180 °C, by dynamic mechanical thermal analysis. Notably, while at temperatures above ~125 °C, ultra-high-molecular-weight polyethylene (UHMWPE) rapidly loses its ability to provide reinforcement due to softening/melting, all PIBOMA resins maintained their ability to reinforce rubber matrix up to 180 °C. For rubber compositions containing 20 phr of PIBOMA, both tensile strength and elongation at break decreased with increasing PIBOMA molecular weight. In summary, PIBOMA, with its outstanding high Tg among known poly(methacrylates), may be used in the preparation of advanced high-stiffness rubber compositions, where it provides reinforcement above 120 °C and gives properties appropriate for a range of applications.


2021 ◽  
Vol 102 (2) ◽  
pp. 63-68
Author(s):  
S. Nikulin ◽  
◽  
V. Verezhnikov ◽  
T. Bulatetskaya ◽  
N. Nikulina ◽  
...  

In the articlethe estimation of coagulating ability using cationic electrolytes is shown.It was found that in the case of using low molecular weight cationic electrolyte, the completeness of the release of rubber from latex is achieved at their consumption of 20–30 kg/t of rubber. A feature of the behavior of cationic surfactants in the latex coagulation has been established. It is shown that the consumption of cationic surfactants corresponds to the consumption of polymer cationic electrolytes. Also, a hypothesis was put forwardthatcationic surfactants violate the aggregate stability of latex systems and the mechanism of action, which is basedon the interaction of cationic surfactant micelles with latex globules carrying anionic surfactants on the surfaceis proposed.The use of cationic surfactants can eliminate the use of sodium chloride in the industry of separating emulsion styrene-butadiene rubber from latex, as well as solve some environmental problems.The final stage of theinvestigationwas to determinethe parametersof rubber compounds and vulcanizates based on the rubber. These rubbers, rubber compounds and vulcanizates correspond to standard parameters.


2020 ◽  
Vol 39 (1) ◽  
pp. 81-90
Author(s):  
An Zhao ◽  
Xuan-Yu Shi ◽  
Shi-Hao Sun ◽  
Hai-Mo Zhang ◽  
Min Zuo ◽  
...  

1999 ◽  
Vol 35 (9) ◽  
pp. 1687-1693 ◽  
Author(s):  
N.S. Saxena ◽  
P. Pradeep ◽  
G. Mathew ◽  
S. Thomas ◽  
M. Gustafsson ◽  
...  

Polymers ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 767 ◽  
Author(s):  
Dániel Simon ◽  
István Halász ◽  
József Karger-Kocsis ◽  
Tamás Bárány

Because of the chemically crosslinked 3D molecular structure of rubbers, their recycling is a challenging task, especially when cost efficiency is also considered. One of the most straightforward procedures is the grinding of discarded rubber products with subsequent devulcanization. The devulcanized rubber can be used as a feedstock for fresh rubber compounds or can be blended with uncured virgin rubber and thermoplastic polymers to form thermoplastic dynamic vulcanizates (TDVs). TDVs combine the beneficial (re)processability of thermoplastics and the elastic properties of rubbers. Our current work focuses on the development of polypropylene (PP)-based TDVs with the use of a tire model rubber (MR) composed of natural rubber (NR) and styrene-butadiene rubber (SBR) in a ratio of 70/30. The research target was the partial substitution of the above fresh MR by microwave devulcanized crumb rubber (dCR). TDVs were produced by continuous extrusion, and the effects of composition (PP/MR/dCR = 40/60/0…50/35/15) and processing parameters (different screw configurations, temperature profiles, the feeding method of PP) were investigated. Results showed that the fresh rubber compound can be replaced up to 10 wt % without compromising the mechanical properties of the resulting TDV.


Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1723 ◽  
Author(s):  
Magdalena Maciejewska ◽  
Anna Sowińska ◽  
Judyta Kucharska

Organic zinc salts and complexes were applied as activators for sulfur vulcanization of styrene–butadiene elastomer (SBR) in order to reduce the content of zinc ions in rubber compounds as compared with conventionally used zinc oxide. In this article, the effects of different organic zinc activators on the curing characteristics, crosslink densities, and mechanical properties of SBR as well as the aging resistance and thermal behavior of vulcanizates are discussed. Organic zinc salts seem to be good substitutes for zinc oxide as activators for sulfur vulcanization of SBR rubber, without detrimental effects to the vulcanization time and temperature. Moreover, vulcanizates containing organic zinc salts exhibit higher tensile strength and better damping properties than vulcanizate crosslinked with zinc oxide. The application of organic zinc activators allows the amount of zinc ions in SBR compounds to be reduced by 70–90 wt % compared to vulcanizate with zinc oxide. This is very important for ecological reasons, since zinc oxide is classified as being toxic to aquatic species.


1965 ◽  
Vol 38 (4) ◽  
pp. 961-966 ◽  
Author(s):  
S. K. Bhatnagar ◽  
S. Banerjee

Abstract Changes in the value of [η], [ηm], K′, (M) and μ of SBR masticated in the cold at 25.0 ± 5.0° C in presence of oxygen with the times of mastication are reported. An empirical relation has been developed between the intrinsic viscosity [η] and Mooney viscosity [ηm] which permits molecular weight of the rubber to be determined directly from Mooney viscosity. The value of g which appears in the Flory equation connecting true crosslink density with the physically determined one has been calculated for unfilled SBR.


2020 ◽  
pp. 000-000 ◽  
Author(s):  
Hyunsung Mun ◽  
Kiwon Hwang ◽  
Gwanghoon Kwag ◽  
JaeKon Suh ◽  
Duseong Ahn ◽  
...  

ABSTRACT In recent years, solution styrene–butadiene rubber (SSBR), which has a narrow molecular weight distribution, controllable microstructure, and chain end functionality, is mainly used as base rubber for passenger car tire tread compounds. However, SSBR has a lower molecular weight than that of emulsion SBR (ESBR) because it is difficult to increase the molecular weight of SSBR. In contrast, ESBR can easily increase the molecular weight; however, it has a broad molecular weight distribution. The reversible addition-fragmentation chain transfer (RAFT) polymerization technique is applicable to the emulsion polymerization. Polymers with narrow molecular weight distributions can be obtained by the RAFT polymerization because the RAFT agent prevents the coupling reaction of the growing chain radicals. In this case, ESBR having a narrow molecular weight distribution, which is an advantage of SSBR, and a high molecular weight, which is an advantage of ESBR, can be synthesized. Therefore, we synthesized RAFT ESBR and fabricated its compounds with silica filler. We confirmed that the physical properties of the RAFT ESBR silica compound are different from those of the ESBR silica compound. In addition to the narrow molecular weight distribution of the RAFT ESBR, the trithiocarbonyl group of the RAFT agent in the RAFT ESBR chain molecules affects the physical properties.


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