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Styrene-butadiene

About: Styrene-butadiene is a research topic. Over the lifetime, 5568 publications have been published within this topic receiving 62099 citations. The topic is also known as: styrene-butadiene rubber & SBR.


Papers
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Journal ArticleDOI
TL;DR: In this paper, a facile and effective approach is developed to obtain the water-dispersible Kevlar nanofibers (KNFs) by modifying KNFs with the assistance of epichlorohydrin (ECH).
Abstract: In this work, a facile and effective approach is developed to obtain the water-dispersible Kevlar nanofibers (KNFs) by modifying KNFs with the assistance of epichlorohydrin (ECH). And the ECH-modified KNFs (m-KNFs) are firstly utilized to prepare styrene–butadiene rubber (SBR)/m-KNFs nanocomposites through latex co-coagulation method. The multifunctional properties of SBR/m-KNFs nanocomposites are thoroughly investigated. It is confirmed that m-KNFs have strong interactions with SBR via π-π stacking, which can generate huge enhancement on the performance of SBR nanocomposites. For example, the tensile strength, tear strength and the maximum decomposition temperature of SBR filled with 7 phr (parts per hundred rubber) m-KNFs are increased by 576%, 202% and 13.1 °C, respectively, compared with those of neat SBR. Meanwhile, the presence of m-KNFs has also improved the dielectric constant of SBR nanocomposites. This work provides a new insight into the fabrication of multifunctional KNFs-based rubber composites.

39 citations

Patent
26 Dec 1979
TL;DR: A multi-layer laminate is defined as a double-layer structure, where layer A is a layer comprising at least one material selected from the group consisting of olefin polymers, polyamide polymers and acrylate polymers; layer B is a modified block copolymer in which an unsaturated carboxylic acid or its derivative is grafted on a styrene-butadiene block copolemer as discussed by the authors.
Abstract: A multi-layer laminate comprising at least one A-B double layer structure, characterized in that said layer A is a layer comprising at least one material selected from the group consisting of olefin polymers, polyamide polymers, acrylate polymers, polyether polymers, polycarbonate polymers, polyurethane polymers, vinylidene chloride polymers, thermosetting resins, vulcanized rubbers, glass and papers and said layer B is a layer comprising mainly a modified block copolymer in which an unsaturated carboxylic acid or its derivative is grafted on a styrene-butadiene block copolymer. Said laminate is excellent in interlaminar adhesion, i.e. peeling strength.

39 citations

Journal ArticleDOI
TL;DR: In this article, a low-pressure gas RF plasma-treatment has been used to improve the adhesion of a synthetic vulcanized rubber to polyurethane adhesive as an environmentally friendly alternative surface treatment to the conventional chemical treatments.
Abstract: A low-pressure gas RF plasma-treatment has been used to improve the adhesion of a synthetic vulcanized rubber to polyurethane adhesive as an environmentally friendly alternative surface treatment to the conventional chemical treatments. A sulfur vulcanized styrene-butadiene rubber (R2) containing a noticeable amount of zinc stearate and paraffin wax (both providing a lack of adhesion) in its formulation was used. Two different gases (oxygen and nitrogen) were used to generate the RF plasma, which was performed at 50 Watt for 1–15 min. The modifications produced on the R2 rubber surface by the RF plasma treatments were assessed by using advancing and receding contact angle measurements, ATR-IR spectroscopy, X-ray Photoelectron Spectroscopy (XPS), Scanning Force Microscopy (SFM), and Scanning Electron Microscopy (SEM). Adhesion evaluation was obtained from T-peel tests of joints produced between plasma treated R2 rubber and a polyurethane adhesive. The plasma treatment produced a decrease in advancing and receding contact angle values on R2 rubber, irrespective to the gas used to generate the RF plasma. The treatment with RF plasma produced the partial removal of hydrocarbon moieties from the rubber surface and the generation of oxygen moieties. An increase in surface roughness was also produced. The degree of oxidation and the amount of hydrocarbon-rich layer removed from the R2 rubber surface was more important by treating with oxygen plasma. The treatment of rubber in oxygen plasma for 1 minute was enough to noticeably increase adhesion of R2 rubber to polyurethane adhesive. However, an extended treatment (15 min.) was needed when nitrogen plasma was applied to R2 rubber. The loci of failure in the joints produced between the plasma treated R2 rubber and the polyurethane adhesive was assessed by using ATR-IR spectroscopy. A mixed failure (partially adhesional and partially cohesive failure in the rubber) in the joints produced with plasma treated R2 rubber joints was always obtained.

39 citations

Journal ArticleDOI
01 Aug 2019
TL;DR: Although CNFs provide much stronger reinforcement than carbon black, going forward, SBR/CNFs/carbon black hybrid nanocomposites can also be developed to offer tailorable property combinations that meet different application requirements.
Abstract: Styrene-butadiene rubber (SBR) is widely used in the tire, footwear, and belt industries. SBR products contain a high content of carbon black, which is hazardous to human health and the environment. The goal of this study is to investigate the potential of using bio-based cellulose nanofibrils (CNFs) as a replacement for carbon black under simulated industrial formula/processing conditions. CNFs were surface-modified using five different reagents to have either -SH or -C=C functional groups grafted onto their surfaces. Vulcanized SBR sheets reinforced with pristine CNFs, and the five functionalized CNFs were prepared and their properties were tested and compared with those of industrial SBR containing carbon black. All the CNFs, pristine or modified, demonstrated higher reinforcing efficiencies (property increase/amount of reinforcement) than carbon black. The modified CNFs showed even higher reinforcing efficiencies than the pristine ones because of the former's better dispersion and stronger interfacial bonding. The -SH and -C=C functional groups reduced the hydrophilicity of CNFs and allowed chemical linkages between CNFs and SBR to be established during vulcanization. Solvent (toluene) resistance of the rubber was also improved after the incorporation of CNFs because of the barrier effect of the nanofibers and the restrained SBR chain mobility. The latter also led to reduced rubber damping. Although CNFs provide much stronger reinforcement than carbon black, going forward, SBR/CNFs/carbon black hybrid nanocomposites can also be developed to offer tailorable property combinations that meet different application requirements.

39 citations

Journal ArticleDOI
TL;DR: In this article, a benzoxazine-functionalized poly(styrene-b-butadiene)-b-styrene) (SBS) has been successfully synthesized via the thiol-ene click reaction.
Abstract: Benzoxazine-functionalized poly(styrene-b-butadiene-b-styrene) (SBS) has been successfully synthesized via the thiol–ene click reaction. Unlike the typical method for fabrication of blends of SBS and thermosetting resins, the benzoxazine could be directly attached on to the chains of PB domains of this triblock copolymer without any prechemical modification for SBS via the incorporation of thiol functionalized benzoxazine (PTMP-BZ). AFM characterization shows that both thiol–ene and subsequent benzoxazine ring-opening reactions have a profound influence on the final morphologies of SBS, which undergoes great change from the cylinders for the pure SBS to different types of lamella structure for the SBS with different contents of the benzoxazines and the results obtained from AFM indicate that the interaction between PB and PS domains is strengthened after two reaction steps and this is responsible for the substantial improvement on the mechanical properties of material including tensile strength and storag...

38 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023118
2022229
2021159
2020239
2019313
2018348