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.

Understanding the thermal properties of zeolites is crucial for their industrial applications. This study explores the thermal stability and dehydration process of clinoptilolite using high-temperature X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Clinoptilolite’s thermal decomposition was monitored from 25 °C to 1200 °C, with results analyzed based on its crystal structure. Principal components analysis (PCA) of the DRIFT spectra indicated progressive water removal and dehydration upon heating, leading to the formation of hydrogen bonds. Thermogravimetric analysis (TGA) revealed a two-step endothermic weight loss: initially, physically adsorbed water was lost up to 100 °C, followed by the removal of tightly bound water and hydroxyl groups until 800 °C. Clinoptilolite remained the dominant phase up to 800 °C, after which albite and cristobalite took over. Rietveld refinement showed that the sample initially contained 70% clinoptilolite, 24% albite, and 6% cristobalite. Above 800 °C, clinoptilolite disappeared, leaving 93% albite and 7% cristobalite. FT-IR spectra changes due to water loss were evident: drying of adsorbed water occurred up to 75 °C and minimal changes were observed from 75 °C to 135 °C, followed by further dehydration until 240 °C. Complete dehydration was confirmed by the disappearance of OH stretching vibration bands by 395 °C, consistent with TGA findings.