For the first time, zirconia nanofibers with an average diameter of about 75 nm have been fabricated by calcination of electrospun zirconium acetylacetonate/polyacrylonitrile fibers in the range of 500–1100 °C. Composite and ceramic filaments have been characterized by scanning electron microscopy, thermogravimetric analysis, nitrogen adsorption analysis, energy-dispersive X-ray spectroscopy, and X-ray diffractometry. The stages of the transition of zirconium acetylacetonate to zirconia have been revealed. It has been found out that a rise in calcination temperature from 500 to 1100 °C induces transformation of mesoporous tetragonal zirconia nanofibers with a high specific surface area (102.3 m²/g) to non-porous monoclinic zirconia nanofibers of almost the same diameter with a low value of specific surface area (8.3 m²/g). The tetragonal zirconia nanofibers with high specific surface area prepared at 500 °C can be considered, for instance, as promising supports for heterogeneous catalysts, enhancing their activity.

Extensive development of the Arctic, rich in various natural resources, requires a lot of cheap ecologically safe construction materials preferably using local renewable sources. Ice being easily available in regions with a cold climate meets all the above criteria but has low strength, high fragility and a tendency to creep. Known strengthening techniques using macroscopic and microfiber additives have many drawbacks. This paper describes a new approach to ice strengthening by adding organic or inorganic 50–100 nm nanoparticles (NPs) to the water to be frozen and presents experimental results and possible mechanisms analysis of polycrystalline ice strengthening using NPs. Cellulose and silica NPs have been tested as typical representatives of such additives. Both are hydrophilic, ecologically safe, widespread, cheap and can be produced from local renewable raw materials. It is shown that the addition of 0.01 to 5 wt.% of NPs results in a reduction of ice composite average grain size by a factor of 5.3 ± 0.7 and an increase of its compression strength by a factor of 2.5 ± 0.3. The highest sensitivity of ice strength to NPs concentration is between 0.1 and 1 wt.%. In this concentration range, the increase in strength is reversely proportional to the square root of the average grain size. Experimental data fit Griffith’s relation better than Hall–Petch, so ice strength is limited by cracks with the length proportional to average grain size.

A Zr-doped CaO sorbent for high-temperature CO₂ capture was fabricated using electrospinning. The nanofiber sorbent with an average filament diameter of about 160 nm is characterized by an initial CO₂ uptake capacity of 12.1 mmol/g, a specific surface area of 79 m²/g, an indentation Young’s modulus of 520 MPa, and a hardness of 1.6 MPa. After 50 carbonation/decarbonation cycles, the sorbent has a decent CO₂ uptake capacity of 9.7 mmol/g due to the uniform distribution of CaZrO₃ in the CaO nanofibers to prevent CaO grain growth caused by CaCO₃ sintering. It is revealed that the sorbent CO₂ uptake capacity decreases both with an increase in the decarbonation temperature and with an increase in the CO₂ concentration in the gas flow upon carbonation, where the sorbent CO₂ uptake capacity is more sensitive to the decarbonation temperature than to the CO₂ concentration in the gaseous stream during carbonation. It is assumed that the electrospun regenerable Zr-doped CaO sorbent is effective for removing CO₂ from flue gases.

The mats of yttria-stabilized tetragonal zirconia nanofibers were prepared using electrospinning. The effect of calcination temperature in the range of 600–1200 °C on their microstructure, phase composition and mechanical properties was investigated. Phase composition of the nanofibers did not change in all ranges of the calcination temperatures, while the average grain size increased from 8 to 39 nm. Nanoindentation testing of the mats showed a decrease in the hysteresis loop energy in samples with higher calcination temperature. Hardness and the elastic modulus measured with the indentation technique were the highest for the mats calcined at 900 °C.

The nanofibrous CaO sorbent for high-temperature CO₂ capture was fabricated by the calcination of electrospun composite filaments containing calcium acetylacetonate and polyacrylonitrile as a calcium-oxide precursor and a binder polymer, respectively. The calcination was carried out in air to prevent PAN carbonization and to obtain pure CaO nanofibers. The resulting mats of CaO nanofibers with the average diameter of 130 nm were characterized by a specific surface area of 31 m²/g, a CO₂-uptake capacity of 16.4 mmol/g at the carbonation temperature of 618 °C, a hardness of 1.87 MPa, and the indentation Young’s modulus of 786 MPa. The low decarbonation temperature makes the fabricated sorbent promising, for example, for the calcium-looping technology of CO₂ removal from the hot exhaust gases of fossil-fueled power plants.