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.

Compatabilization of polystyrene/polypropylene blends by styrene–butadiene block copolymers with differing polystyrene block lengths

Abstract: Compatibilization of polystyrene/polypropylene (PS/PP) blends, by use of a series of butadiene–styrene block copolymers was studied by means of small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). The compatibilizers used differ in molar mass and the number of blocks. It was shown that the ability of a block copolymer (BC) to participate in the formation of an interfacial layer (and hence in compatibilization) is closely associated with the molar mass of styrene blocks. If the styrene blocks are long enough to form entanglements with the styrene homopolymer in the melt, then the BC is trapped inside this phase of the PS/PP blends, and its migration to the PS/PP interface is difficult. In this case, the BC does not participate in the formation of the interfacial layer nor, consequently, in the compatibilization process. On the other hand, the BC's with the molar mass of the PS blocks below the critical value are proved to be localized at the PS/PP interface. This preferable entrapping of some styrene–butadiene BC's in the PS phase of the PS/PP blend is, of course, connected to the differing miscibility of the BC blocks with corresponding components of this blend. Although the styrene block is chemically identical to the styrene homopolymer in the blend, the butadiene block is similar to the PP phase. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1647–1656, 1999

Ordered structures of styrene-butadiene block copolymers in the solid state

Abstract: Several narrow molecular weight distribution block copolymers were prepared by a two-stage anionic polymerization technique. Films cast from these solutions were studied by electron microscopy. Replicas showed that the film surfaces were composed of layered structures with various orientations. Micrographs of ultrathin sections of stained films demonstrate that layered structure occur throughout the film. The widths of the copolymer layer spacings increase with increasing molecular weight and agree quite well with the calculated values.

Influence of Silica and its Different Surface Treatments on the Vulcanization Process of Silica Filled SBR

Abstract: The effect of different silica treatments on the vulcanization of silica filled Styrene Butadiene Rubber (SBR) is investigated. The concentration, the length and the functionality (coupling or non coupling) of the silane used for this treatment are the parameters studied. It is shown that the silane grafting, by covering the silica surface, modifies the adsorption and desorption on this surface of the accelerators used in the vulcanization system, which in turn modifies the crosslinking kinetic and therefore should influence the final crosslinking state of the matrix.

Preparation, characterization, and application of NR/SBR/Organoclay nanocomposites in the tire industry

Abstract: The natural rubber/styrene butadiene rubber/organoclay (NR/SBR/organoclay) nanocomposites were successfully prepared with different types of organoclay by direct compounding. The optimal type of organoclay was selected by the mechanical properties characterization of the NR/SBR/organoclay composites. The series of NR/SBR/organoclay (the optimal organoclay) nanocomposites were prepared with various organoclay contents loading from 1.0 to 7.0 parts per hundreds of rubber (phr). The nearly completely exfoliated organoclay nanocomposites with uniform dispersion were confirmed by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The results of mechanical properties measurement showed that the tensile strength, tensile modulus, and tear strength were improved significantly when the organoclay content was less than 5.0 phr. The tensile strength and the tear strength of the nanocomposite with only 3.0 phr organoclay were improved by 92.8% and 63.4%, respectively. It showed organoclay has excellent reinforcement effect with low content. The reduction of the score and cure times of the composites indicated that the organoclay acted as accelerator in the process of vulcanization. The incorporation of a small amount of organoclay greatly improved the swelling behavior and thermal stability, which was attributed to the good barrier properties of the dispersed organoclay layers. The outstanding performance of co-reinforcement system with organoclay in the tire formulation showed that the organoclay had a good application prospect in the tire industry, especially for the improvement of abrasion resistance and the reduction of production cost. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011