Using a sulfur-bearing silane to improve rubber formulations for potential use in industrial rubber articles

This is an Accepted Manuscript of an article published by Taylor & Francis in Journal of Adhesion Science and Technology on 13/08/2012, available online: http://dx.doi.org/10.1080/01694243.The availability of the coupling agent bis (3-triethoxysilylpropyl)-tetrasulfide (TESPT) has provided an opportunity for enhancing the reinforcing capabilities of precipitated amorphous white silica in rubber. Styrene-butadiene rubber, synthetic polyisoprene rubber (IR), acrylonitrile-butadiene rubber, and natural rubber (NR) containing the same loading of a precipitated silica filler were prepared. The silica surface was pretreated with TESPT, which is a sulfur-bearing bifunctional organosilane to chemically bond silica to the rubber. The rubber compounds were subsequently cured by reacting the tetrasulfane groups of TESPT with double bonds in the rubber chains and the cure was optimized by adding sulfenamide accelerator and zinc oxide. The IR and NR needed more accelerators for curing. Surprisingly, there was no obvious correlation between the internal double bond content and the accelerator requirement for the optimum cure of the rubbers. Using the TESPT pretreated silanized silica was a very efficient method for cross-linking and reinforcing the rubbers. It reduced the use of the chemical curatives significantly while maintaining excellent mechanical properties of the cured rubbers. Moreover, it improved health and safety at work-place, reduced cost, and minimized damage to the environment because less chemical curatives were used. Therefore, TESPT was classified as "green silane" for use in rubber formulations

REVIEW OF THE RECLAIMING OF RUBBER WASTE AND RECENT WORK ON THE RECYCLING OF ETHYLENE–PROPYLENE–DIENE RUBBER WASTE

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Rubber Chemistry and Technology, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.5254/rct.15.84850.Rubbers do not decompose easily and therefore disposal of rubber waste is a serious environmental concern. Raw material costs, diminishing natural resources, and the growing awareness of environmental issues and sustainability have made rubber recycling a major area of concern. Reclaiming and recycling rubber waste is a major scientific and technological challenge facing rubber scientists today. This paper reviews a number of important areas related to the reclaiming, characterizing, testing and recycling of rubber waste. These include: chemical and microbial devulcanization with particular emphasis on main chain scission and kinetics of chemical devulcanization reactions; the cutting-edge techniques for reclaiming devulcanized rubber waste by the action of large shearing forces, heat and chemical agents: and analytical techniques and methods for characterizing composition and testing of devulcanized rubber waste, respectively. In addition, some aspects of the recycling of devulcanized ethylene-propylene-diene rubber (EPDM) waste will be reported. EPDM is used extensively in automotive components world-wide and recycling the rubber at the end of its useful service life is of major importance to manufacturers of automotive components

Preparation and characterization of natural rubber/silica nanocomposites using rule of similarity in latex

Rule of similarity and latex compounding techniques were combined for the first time to prepare natural rubber/nanosilica (NR/SiO2) nanocomposite with core-shell nanosilica-poly (methyl methacrylate) (SiO 2-PMMA) particles and PMMA-modified natural rubber matrix (NR-PMMA). The microstructure of SiO2 and nanocomposites with different SiO 2 contents was characterized by fourier transform infrared spectroscopy (FTIR); the morphology of nanocomposites was investigated with scanning electron microscopy (SEM); the tensile strength was characterized by tensile testing machine and the thermal stability of composites was studied by thermal gravimetric analysis. Results showed that PMMA chains have successfully grafted onto the surface of SiO2, and the core-shell SiO 2-PMMA nanoparticles and NR-PMMA latex have been perfectly incorporated. SiO2-PMMA nanoparticles are evenly distributed over the NR matrix with an average size in the range of 60-100 nm at the low content (SiO2? 3 wt%), while aggregations are apparently observed when 5 wt% SiO2 is loaded. In addition, NR/SiO2 composities possess a considerable improvement in ageing resistance compared with the pure NR. The tensile strength of composite increases from 6.99 to 12.72 MPa, reaching the highest value at a 0.5 wt% SiO2 loading, and then the figure decreases gradually because of the aggregation of SiO2 nanoparticles. It is anticipated that the reported process is to provide a simple and economic way for preparing NR composites