The physico-mechanical, chemical and mineralogical characteristics of volcanic glass (perlite) from the Mariovo region (Macedonia) as well as the mineralogical changes that occur during its thermal treatment were investigated to demonstrate its utilization for industrial use. The native perlite was characterized by chemical analysis, X-ray powder diffraction (XRPD), infrared (IR) spectroscopy, thermal analysis (TGA/DTA), scanning electron microscopy (SEM-EDX), transmission electron microscopy (TEM), and solid-state NMR. The chemical examination suggests that the perlite represents an acidic volcanic rock with a high percentage of SiO 2 (72.45%), high in alkali metal oxides (4.21 wt.% K 2 O, 3.56 wt.% Na 2 O), with a loss of ignition 3.54 wt.%. Results from the XRPD indicated major amorphous behaviour, with low amounts of feldspars, quartz, and cristobalite. SEM examinations revealed glassy structure with presence of certain pores (dimensions ranging from 50-100 μm). The determined expansion coefficient was 20 times its original volume. XRPD of expanded perlite compared to the native perlite depicted new intensive peaks of cristobalite. SEM and TEM revealed irregular morphology with broken or ragged edges. On the basis of the chemical and mineralogical composition, the studied perlite is classified as an appropriate material suitable as ceramic flux to lower the sintering temperature.

The diatomaceous earth (DE), collected from the Mariovo region in North Macedonia, was characterized and thermally modified. The material represents a sedimentary rock of biogenic origin, soft solid that can be easily disintegrated, with white to grayish color, with bulk density of 0.51–0.55 g/cm3, total porosity of 61–63%, and specific gravity of 2.25 g/cm3. The chemical composition is as follows: SiO2, 86.03; Al2O3, 3.01; Fe2O3, 2.89; MnO, 0.06; TiO2, 0.20; CaO, 0.76; MgO, 0.28; K2O, 0.69; Na2O, 0.19; P2O5, 0.15; and loss of ignition, 5.66 (wt%). The mineralogy of the raw DE is characterized by the predominant presence of amorphous phase, followed by crystalline quartz, muscovite, kaolinite, and feldspar. Significant changes in the opal phase are observed in the 1,000–1,200°C temperature region. At 1,100°C, the entire opal underwent solid–solid transition to cristobalite. Further ramp of the temperature (1,100–1,200°C) induced formation of mullite. Scanning electron microscopy (SEM) and transmission electron microscopy depict the presence of micro- and nanostructures with pores varying from 260 to 650 nm. SEM analysis further determined morphological changes in terms of the pore diameters shrinkage to 120–250 nm in comparison to the larger pores found in the initial material. The results from this investigation improve the understanding of mechanism of silica phase transition and the relevant phase alterations that took place in DE upon calcination temperatures from 500 to 1,200°C.

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Hydroxyapatite is a particularly attractive material for human tissue implantation. The intrinsic poor mechanical properties of hydroxyapatite material can lead to instability and unsatisfactory duration of the implant in the presence of body fluids and local loading. Addition of TiO2 in the hydroxyapatite matrix can enhance the mechanical properties of the obtained composite. The composite with 15 % TiO2 content shows a thermal stability of the system and improved mechanical properties

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