The aim of this work is to describe the changes in the properties of ceramifiable silicone rubber-based composites caused by the incorporation of novel alternative minerals in comparison to other popular, widely utilized fillers. TiO₂, calcined kaolin and calcium-based minerals mix (CbMix) consisting of CaO (6.26 wt%), CaCO₃ (26.18 wt%) and Ca(OH)₂ (67.56 wt%) have not been considered as a dispersed phase of ceramifiable silicone composites destined for wire covers yet. Mineral fillers: TiO₂ (anatase), mica (phlogopite), CbMix, CaCO₃, Al(OH)₃, kaolin and calcined kaolin affect the processing and the various properties of silicone rubber-based composites destined for wire covers differently. The properties—flammability, smoke intensity, micromorphology and mechanical durability after ceramification—are assessed by measuring: the kinetics of vulcanization, stress at different levels of elongation, tensile strength and the elongation at break of the materials. Although the curing process of the composites is disturbed by the addition of CbMix, it benefits from an increase in oxygen index value, which reaches 31.4%. What is more, also its flammability parameters measured by cone calorimetry improve, such as the total heat released (THR) reaching 9.3 MJ/m². Samples containing kaolin and calcined kaolin exhibit the best mechanical properties before ceramification, whereas composites filled with calcium-based powders (CbMix, CaCO₃) mechanically display the strongest mineral char after heat treatment, possibly due to a more homogenous micromorphology and the creation of calcium silicates at elevated temperature. Significant amounts of wollastonite, parawollastonite and pseudowollastonite are visible in their structure after ceramification.

Ceramifiable styrene-butadiene (SBR)-based composites containing low-softening-point-temperature glassy frit promoting ceramification, precipitated silica, one of four thermally stable refractory fillers (halloysite, calcined kaolin, mica or wollastonite) and a sulfur-based curing system were prepared. Kinetics of vulcanization and basic mechanical properties were analyzed and added as Supplementary Materials. Combustibility of the composites was measured by means of cone calorimetry. Their thermal properties were analyzed by means of thermogravimetry and specific heat capacity determination. Activation energy of thermal decomposition was calculated using the Flynn-Wall-Ozawa method. Finally, compression strength of the composites after ceramification was measured and their micromorphology was studied by scanning electron microscopy. The addition of a ceramification-facilitating system resulted in the lowering of combustibility and significant improvement of the thermal stability of the composites. Moreover, the compression strength of the mineral structure formed after ceramification is considerably high. The most promising refractory fillers for SBR-based ceramifiable composites are mica and halloysite.

The paper presents the test results of the effect of modified graphene and multi-wall carbon nanotubes on the thermal and mechanical properties and flammability of acrylic rubber and styrene-butadiene rubber. The rubbers were cross-linked with the use of organic peroxide. Based on the test results obtained by optic and AFM methods, a relationship between the surface morphology of the nanocomposites obtained was presented. By means of thermal analysis methods (TG, DTG, DTA) and a micro-calorimeter, it has been found that the nanofillers used considerably increase the thermal stability and decrease flammability of the nanocomposites. The mechanical properties of the elastomeric materials obtained depend on the type and content of nanofiller.

In modern polymer industry, there still is a room for new generations of fillers capable of enhancing the performance of composite materials. Currently, much effort is being put into a process of improving mechanical properties of elastomer materials. In this work, multiwalled carbon nanotubes (MWCNTs) and graphene nanoplatelets (GnPs) were modified with silane, titanate, or zirconate using plasma treatment, in order to apply them as fillers for styrene/butadiene rubber. Following its modification, filler surface was analyzed: Surface free energy (SFE) was measured with tensiometry, and micromorphology and chemical composition were studied with scanning electron microscopy–energy-dispersive spectroscopy (SEM–EDS), while elemental composition and bonding were assessed with X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). Low-temperature oxygen plasma activation of MWCNT fillers leads to a significant increase in the SFE polar component, with the same effect being much weaker for GnP fillers. Grafting silanes, zirconates, and titanates on activated filler surface results in a decrease in SFE polar component—surface oxygen-containing active groups react with silane/zirconate/titanate molecules. Fillers modified in this way exhibit different micromorphology and surface chemical composition what is revealed with the SEM–EDS, ToF-SIMS, and XPS techniques. As the ultimate step, either MWCNT or GnP rubber nanocomposites were manufactured using the modified fillers with their mechanical properties and cross-link density being studied. Filler modification resulted in substantial changes both in composite performance, and in its cross-linking density. In the case of modified filler containing composites, improved tensile strength and elongation at break were observed.

Ground tire rubber (GTR) is used to decrease the cost of vulcanizates. However, insufficient interactions between GTR particles and rubber matrices make mechanical properties of vulcanizates containing GTR deteriorate. This paper compares original methods of GTR modification. The effects of surface activation of GTR by sulfuric acid (A), its modification by (3-mercaptopropyl)trimethoxy silane (M), or the hybrid treatment—combining both approaches (H), were analyzed in terms of surface energy, specific surface area and morphology of GTR particles. Vulcanizates containing virgin GTR were compared to the rubber filled with the modified GTR particles keeping the same amount of CB in the rubber mix, according to their crosslink density, mechanical and tribological properties. Contrary to the virgin GTR, the addition of modified GTR increases the stiffness of the vulcanizates. The highest changes have been observed for the samples filled with ca. 12 phr of the GTR modified with silane and ca. 25 phr of the GTR subjected to the hybrid treatment, representing the highest crosslink density of rubber vulcanizates filled with GTR. Furthermore, the addition of modified GTR, especially in the case of the samples where 10 phr of rubber was replaced, results in the significant lowering of friction but higher abrasive wear.

This paper describes a method of laser ablation for improving the hydrophobic properties of vulcanized rubber. The treatment was tested on acrylonitrile rubber (NBR) and styrene butadiene rubber (SBR) containing carbon nanotubes and soot as fillers. The surface layer of the vulcanizates was modified using a nanosecond-pulsed laser at 1060 nm wavelength. The parameters of the ablation process were congruent, so no chemical changes in the polymeric material were observed. Evaluation of the surface condition of the laser-textured samples was performed using a Leica MZ6 stereoscopic microscope, operating with MultiScan 8.0 image analysis software. The contact angles were determined for all the samples before and after the surface modification process. Following modification of the surface morphology, with the best parameters of laser ablation, the contact angle increased, reaching 147°, which is very close to the threshold of superhydrophobicity (150°). On the basis of the results from several tests, laser ablation with a fiber-pulsed laser can be considered a very useful method for producing rubbers with superhydrophobic surfaces.