It is generally believed that only intermolecular, elastically-effective crosslinks influence elastomer properties. The role of the intramolecular modifications of the polymer chains is marginalized. The aim of our study was the characterization of the structural parameters of cured elastomers, and determination of their influence on the behavior of the polymer network. For this purpose, styrene-butadiene rubbers (SBR), cured with various curatives, such as DCP, TMTD, TBzTD, Vulcuren^®, DPG/S₈, CBS/S₈, MBTS/S₈ and ZDT/S₈, were investigated. In every series of samples a broad range of crosslink density was obtained, in addition to diverse crosslink structures, as determined by equilibrium swelling and thiol-amine analysis. Differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) were used to study the glass transition process, and positron annihilation lifetime spectroscopy (PALS) to investigate the size of the free volumes. For all samples, the values of the glass transition temperature (T_g) increased with a rise in crosslink density. At the same time, the free volume size proportionally decreased. The changes in T_g and free volume size show significant differences between the series crosslinked with various curatives. These variations are explained on the basis of the curatives’ structure effect. Furthermore, basic structure-property relationships are provided. They enable the prediction of the effect of curatives on the structural parameters of the network, and some of the resulting properties. It is proved that the applied techniques—DSC, DMA, and PALS—can serve to provide information about the modifications to the polymer chains. Moreover, on the basis of the obtained results and considering the diversified curatives available nowadays, the usability of “part per hundred rubber” (phr) unit is questioned.

This paper presents an overview of alternative uses for products of sugar beet processing, especially sucrose, as chemical raw materials for the production of biodegradable polymers.

Ceramizable (ceramifiable) silicone rubber-based composites are modern elastomeric materials for fire protection application. The most important sector of economy using such materials is cable industry because there are special types of electric circuits that have to keep working in the case of fire. These kinds of composites can create ceramic phase protecting copper wire from melting under high temperature. When temperature increases, polymer matrix degrades (creating silica residue as one of the products) and mineral particles dispersed in silicone rubber matrix stick together creating stiff, durable, insulating and porous ceramic skin. In this paper, the influence of surface modification of montmorillonite with quaternary ammonium salts on ceramization of their silicone rubber composites is presented. Filler modification was studied, determining changes to its surface energy and thermal stability. Mechanical properties, flammability and thermal stability of composites were determined. Ceramization of the composites was discussed from the point of view of their mechanical properties and structure of ceramic phase after heat treatment, determined by compression stress tests, porosimetry and scanning electron microscopy adequately. Results show that type of modifier applied strongly affects properties of silicone rubber-based ceramizable composites before and after ceramization. Samples containing surface-modified montmorillonite produce significantly less heat during their thermal decomposition than composite filled with unmodified montmorillonite. Moreover, incorporation of montmorillonite modified with ammonium salt of linear organic chain causes the creation of nano-porous structure after ceramization. On the one hand, it facilitates heat insulation, but on the other hand, high total volume of pores adversely affects mechanical endurance of the ceramic phase.

Ceramizable (ceramifiable) silicone composites are one of the most important elastic technical materials produced industrially. These composites are commonly used to increase flame retardancy of electrical cables and to ensure integrity of electricity network during fire by their ability to create a continuous ceramic structure. In this paper, ceramizable silicone composites filled with different contents of carbon fibers were tested. The research was focused on the characterization of ceramic structure created during heat treatment of the composites and thermal properties of the composites. For this purpose, morphology (SEM) and compression strength of the ceramic structures were studied. To describe process of ceramic structures creation, TG/DSC analysis was done. These tests have demonstrated that, the increase in carbon fibers amount improves the mechanical properties of ceramic structure regardless of heat treatment conditions.

It is widely acknowledged that waste sulfur generated from the petroleum industry creates huge storage and ecological problems. Therefore, the various methods of utilization are becoming increasingly attractive research topics worldwide. The thermal ability of elemental sulfur to homolytic cleavage of S₈ rings enables its free radical copolymerization with unsaturated organic species and the obtaining of chemically stable polymeric materials. Here we report a novel possibility to use sulfur/organic copolymers obtained via “inverse vulcanization” as curatives for rubber. For this purpose, several various sulfur/organic copolymers were synthesized and analyzed from the point of view of their performance as rubber crosslinking agents. Solvent extraction was used to purify sulfur/organic copolymers from unreacted (elemental) sulfur. Thermal properties of the prepared copolymers were characterized by thermogravimetric analysis and differential scanning calorimetry (TGA–DSC). Crosslink density and structure of cured elastomers was studied by equilibrium swelling, thiol-amine analysis and freezing point depression. Mechanical properties of the vulcanizates were determined under static and dynamic conditions (DMA—dynamic mechanical analysis). It is proved that the utilization of sulfur/organic copolymers as curatives enables an effective crosslinking process of rubbers. Taking into account the results of a crosslink density analysis and mechanical properties of the vulcanizates cured with purified copolymers, it is evident that relatively long copolymer macromolecules are also involved in the formation of chemical bonds between unsaturated rubber macromolecules.