Composite powders were synthesized from the water solutions of sodium silicate and different calcium salts (nitrate, chloride, and acetate) at a Ca/Si molar ratio of 1.0. According to the XRD data, all the synthesized powders included hydrated calcium silicate Ca_1,5SiO_3,5·xH₂O (Ca/Si molar ratio = 1.5) and calcium carbonate CaCO₃ (Ca/Si molar ratio = ∞). The presence of H₂SiO₃ or SiO₂·xH₂O in the synthesized powders was assumed to be due to the difference between the Ca/Si molar ratio of 1.0 specified by the synthesis protocol and the molar ratio of the detected products. Reaction by-products (sodium nitrate NaNO₃, sodium chloride NaCl, and sodium acetate NaCH₃COO) were also found in the synthesized powders after filtration and drying. According to the XRD data phase composition of all powders after washing four times consisted of the quasi-amorphous phase and calcium carbonate in the form of calcite. Calcium carbonate in the form of aragonite was detected in powders synthesized from calcium chloride CaCl₂ and calcium nitrate Ca(NO₃)₂ before and after washing. Synthesized powders containing reaction by-products and washed powders were used for the preparation of ceramics at 900, 1000, and 1100 °C. The phase composition of the ceramic samples prepared from the washed powders and powder containing NaCl after firing at 900 and 1000 °C consisted of β-wollastonite β-CaSiO₃, and, after firing at 1100 °C, consisted of both β-wollastonite β-CaSiO₃ and pseudo-wollastonite α-CaSiO₃. The phase composition of the ceramic samples prepared from powders containing sodium nitrate NaNO₃ and sodium acetate NaCH₃COO after firing at 900, 1000, and 1100 °C consisted of calcium sodium silicates, i.e., Na₂Ca₂Si₃O₉ (combeite) and Na₂Ca₃S_i2O₈. Synthesized and washed composite powders can be used for the preparation of biocompatible materials, in the technology of construction materials, and as components of lunar soil simulants.

Powders with a phase composition including syngenite (K₂Ca(SO₄)₂·H₂O) and/or calcium sulfate dihydrate (gypsum, CaSO₄·2H₂O) were synthesized from the powder of calcium carbonate (CaCO₃) and water solutions of potassium hydrosulfate (KHSO₄) of various concentrations (0.5 M, 1 M, and 2 M). A molar ratio of starting salts, KHSO₄/CaCO₃ = 2, was used to provide the formation of syngenite (K₂Ca(SO₄)₂·H₂O). But when using a 0.5 M water solution of potassium hydrosulfate (KHSO₄), the phase composition of the synthesized powder was presented by calcium sulfate dihydrate (gypsum, CaSO₄·2H₂O). When using 1 M and 2 M water solutions of potassium hydrosulfate (KHSO₄), the syngenite (K₂Ca(SO₄)₂·H₂O) was found as the predominant phase in synthesized powders. According to estimations made from thermal analysis data, powders synthesized using 1.0 M and 2.0 M water solutions of potassium hydrosulfate (KHSO₄) contained no more than 7.9 and 1.9 mass % of calcium sulfate dihydrate (gypsum, CaSO₄·2H₂O), respectively. The phase composition of products isolated from mother liquors via water evaporation consisted of syngenite (K₂Ca(SO₄)₂·H₂O) and potassium sulfate (arcanite, K₂SO₄). Synthesized powders can be used in preparation of biocompatible bioresorbable materials with phase compositions in the K₂O-CaO-SO₃-H₂O system; as matrix of thermo- or photo-luminescent materials; as components reducing the setting time and increasing the strength of sulfate cements; in the fertilizing industry; and also as components of Martian regolith simulants.

Powders with phase composition including quasi-amorphous phases and calcium carbonate CaCO₃ in the form of calcite or aragonite and sodium halite NaCl as a reaction by-product were synthesized from 0.5M aqua solutions of sodium silicate and 0.5M aqua solutions of calcium and/or magnesium chlorides. Starting solutions were taken in quantities which could provide precipitation of hydrated calcium and/or magnesium silicates with molar ratios Ca/Si = 1 (CaSi), Mg/Si = 1 (MgSi) or (Ca+Mg)/Si = 1 (CaMgSi). Hydrated calcium and/or magnesium silicates, hydrated silica, magnesium carbonate, hydrated magnesium carbonate or hydrated magnesium silicate containing carbonate ions are suspected as components of quasi-amorphous phases presented in synthesized powders. Heat treatment of synthesized powders at 400, 600, 800 °C and pressed preceramic samples at 900, 1000, 1100 and 1200 °C were used for investigation of thermal evolution of the phase composition and microstructure of powders and ceramic samples. Mass loss of powder samples under investigation during heat treatment was provided due to evacuation of H₂O (m/z = 18), CO₂ (m/z = 44) and NaCl at temperatures above its melting point. After sintering at 1100 °C, the phase composition of ceramic samples included wollastonite CaSiO₃ (CaSi_1100); enstatite MgSiO₃, clinoenstatite MgSiO₃ and forsterite Mg₂SiO₄ (MgSi_1100); and diopside CaMgSi₂O₆ (CaMgSi_1100). After sintering at 1200 °C, the phase composition of ceramics CaSi_1200 included pseudo-wollastonite CaSiO₃. After heat treatment at 1300 °C, the phase composition of MgSi_1300 powder included preferably protoenstatite MgSiO₃. The phase composition of all samples after heat treatment belongs to the oxide system CaO–MgO–SiO₂. Ceramic materials in this system are of interest for use in different areas, including refractories, construction materials and biomaterials. Powders prepared in the present investigation, both via precipitation and via heat treatment, can be used for the creation of materials with specific properties and in model experiments as lunar regolith simulants.

Powders with phase composition including syngenite K2Ca(SO4)2·H2O and/or calcium sulfate di-hydrate (gypsum) CaSO4·2H2O were synthesized from powder of calcium carbonate CaCO3 and water solutions of potassium hydrosulfate KHSO4 of various (0.5M, 1M and 2M) concentrations. Molar ratio of starting salt KHSO4/CaCO3=2 were used to provide formation of syngenite K2Ca(SO4)2·H2O. But when using 0.5M water solution of potassium hydrosulfate KHSO4 the phase composition of synthesized powder was presented by calcium sulfate dihydrate (gypsum) CaSO4·2H2O. When using 1M and 2M water solution of potassium hydrosulfate KHSO4 the syn-genite K2Ca(SO4)2·H2O was found as predominant phase in synthesized powders. According es-timations made from thermal analysis data when 1.0M and 2.0M water solutions of potassium hydrosulfate KHSO4 were used the content of calcium sulfate dihydrate (gypsum) CaSO4·2H2O in these powders were not higher then as 7.9 and 1.9 % respectively. Phase composition of products isolated from mother liquors via water evaporation consisted of syngenite K2Ca(SO4)2·H2O and potassium sulfate (arcanite) K2SO4. Synthesized powders can be used in preparation of biocom-patible bioresorbable materials with phase composition in the K2O‑CaO‑SO3‑H2O system; as matrix of thermo- or photo-luminescent materials; as components reducing the setting time and increasing strength of sulfate cements; in the fertilizing industry and also as a components of Martian regolith simulant.