The technological mode of obtaining amorphous SiO2 nanopowders based on hydrothermal solutions is proposed in this study. Polycondensation of orthosilicic acid as well as ultrafiltration membrane separation, and cryochemical vacuum sublimation were used. The characteristics of nanopowders were determined by tunneling electron microscopy, low-temperature nitrogen adsorption, X-ray diffraction, and small-angle X-ray scattering. The scheme allows to adjust density, particle diameters of nanopowders, specific surface area, as well as diameters, area and volume of the pore. Thus, the structure of nanopowders is regulated-the volume fraction of the packing of spherical particles in aggregates and agglomerates, the size of agglomerates, and the number of particles in agglomerates. The pour densities of the nanopowders depend on the SiO2 content in sols, which were 0.02 to 0.3 g/cm3. Nanoparticles specific surface area was brought to 500 m2/g by low temperature polycondensation. Nanoparticle aggregates specific pore volume (0.2-0.3 g/cm3) weakly depend on powders density. The volume fraction of the packing of SiO2 nanoparticles in aggregates was 0.6-0.7. Solid samples of compacted nanopowders had a compressive strength of up to 337 MPa. Possible applications of hydrothermal SiO2 nanopowders are considered.
Keywords: cryochemical vacuum sublimation; diameter of SiO2 nanoparticles; hydrothermal solution; nanopowder structure; polycondensation of orthosilicic acid; ultrafiltration membrane separation.