The antibacterial performance and cytotoxic examination of in situ prepared silver nanoparticles (Ag NPs), on inorganic-organic hybrid nanopowder consisting of zirconium dioxide nanoparticles (ZrO₂ NPs) and dihydroquercetin (DHQ), was performed against Gram (−) bacteria Escherichia coli and Gram (+) bacteria Staphylococcus aureus, as well as against human cervical cancer cells HeLa and healthy MRC-5 human cells. The surface modification of ZrO₂ NPs, synthesized by the sol-gel method, with DHQ leads to the interfacial charge transfer (ICT) complex formation indicated by the appearance of absorption in the visible spectral range. The prepared samples were thoroughly characterized (TEM, XRD, reflection spectroscopy), and, in addition, the spectroscopic observations are supported by the density functional theory (DFT) calculations using a cluster model. The concentration- and time-dependent antibacterial tests indicated a complete reduction of bacterial species, E. coli and S. aureus, for all investigated concentrations of silver (0.10, 0.25, and 0.50 mg/mL) after 24 h of contact. On the other side, the functionalized ZrO₂ NPs with DHQ, before and after deposition of Ag NPs, do not display a significant decrease in the viability of HeLa MRC-5 cells in any of the used concentrations compared to the control.

Several recent studies have evaluated technologies of spent nuclear fuel processing specifically for solidifying transuranic (TRU) waste as a by-product of fission. Of the TRU group, plutonium and the minor actinides will be responsible for the bulk of the radiotoxicity and heat generation of spent nuclear fuel in the long term (300 to 20,000 years). In this study, we investigated magnesium potassium phosphate (MKP)-based compounds as host waste forms for the encapsulation of inactive trivalent Nd and Sm as analogues of the minor trivalent actinides, Am and Cm. Waste forms were fabricated under ambient atmospheric conditions by adding 5 wt.% of substances containing Nd or Sm via the following two routes: powder oxides and aqueous solutions of nitrate salts. Waste form performance was established using strength and aqueous medium leaching tests of MKP-based specimens. The MKP materials were analyzed by X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM and TEM), energy-dispersive X-ray spectroscopy (EDS), and Raman spectroscopy. The waste forms exhibited a compressive strength of ≥30 MPa and were durable in an aqueous environment. The leachability indices for Nd and Sm, as per the ANS 16.1 procedure, were 19.55–19.78 and 19.74–19.89, respectively, which satisfy the acceptable criteria (>6). The results of the present room temperature leaching study suggest that MKPs can be effectively used as a host material to immobilize actinides (Am and Cm) contained in TRU waste.

Controlled porosity with precise pore sizes in carbon monoliths (CMs) is crucial for optimizing performance in electrochemical energy storage and adsorption applications. This study explores the influence of porosity in CMs, developed from polymer precursors via the sol–gel route, employing soft templating, in situ graphene growth, and post-activation. The effects on CO₂ and H₂ sorption and electrochemical capacitor (EC) performance are analyzed. Graphene is successfully grown in situ from graphene oxide (GO), as confirmed by several characterization analyses. The amount of GO incorporated influences the crosslink density of the polymer gel, generating various pore structures at both micro- and mesoscales, which impacts performance. For instance, CO₂ capture peaks at 5.01 mmol g⁻¹ (0 °C, 101 kPa) with 10 wt % GO, due to the presence of wider micropores that allow access to ultramicropores. For H₂ storage, the best performance is achieved with 5 wt % GO, reaching 12.8 mmol g⁻¹ (−196 °C, 101 kPa); this is attributed to the enlarged micropore volumes between 0.75 and 2 nm that are accessible by mesopores of 2 to 3 nm. In contrast, for the ECs, lower GO loadings (0.5 to 2 wt %) improve ion accessibility via mesopores (4 to 6 nm), enhancing rate capability through better conduction.

This work deals with Cu-modified 1DTiO₂ microrods (MRs) and their surface properties. The pristine lyophilized precursor Cu_1DTiO₂, prepared by an environmentally friendly cryo-lyophilization method, was further annealed in the temperature interval from 500 to 950 °C. The microstructure of all samples was characterized by electron microscopy (SEM/EDS and HRTEM/SAED), X-ray powder diffraction (XRD), infrared spectroscopy, simultaneous DTA/TGA thermoanalytical measurement, and mass spectroscopy (MS). Special attention was paid to the surface structure and porosity. The 1D morphology of all annealed samples was preserved, but their surface roughness varied due to anatase-rutile phase transformation and the change of the nanocrystals habits due to nanocavities formation after releasing of confined ice-water. The introduction of 2 wt.% Cu as electronically active second species significantly reduced the direct bandgap of 1DTiO₂ in comparison with undoped TiO₂ and the standard Degussa TiO₂_P25. All samples were tested for their UV absorption properties and H₂ generation by PEC water splitting. We presented a detailed study on the surface characteristics of Cu doped 1DTiO₂ MRs due to gain a better idea of their photocatalytic activity.

Synthesis of mesoporous alumina made by nanocasting using polymer spheres matrix is reported. In contrast to all other recipes described in the literature so far, mesoporous alumina prepared by the nanocasting method consists of irregularly ordered particles exhibiting pores of ca. 25 nm in size. The void volume among the particles constitutes a porous system with narrow pore size distribution in the mesopore region.

We report on the study of the immobilization process of non-radioactive rhenium (Re), a chemical analogue of technetium-99 (⁹⁹Tc), in compounds based on magnesium potassium phosphate (MKP), as well as the possibility of enhancing their properties with iron-bearing additives/fillers. Powdered Re₂O₇ was used as the initial Re-containing source. Because of the solubility and high leachability of Tc (VII), which is also volatile at high temperatures, its immobilization for long-term storage and disposal poses a serious challenge to researchers. Taking this into account, low-temperature stabilization technology based on MKP, a cementitious material, is currently considered promising. We prepared experimental specimens based on Re-incorporated MKP matrices and analyzed their microstructure in detail using analytical methods of X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Considering that iron-bearing substances can reduce Tc (VII) to the lower-valence form Tc (IV), which is more stable, attention was also paid to evaluate the effect of fillers (Fe₂O₃, Fe₃O₄, Fe, FeS and blast furnace slag (BFS)) on strength, oxidation state, and water resistance (expressed as leaching cumulative concentration). The addition of fillers ensures the formation of denser compounds based on MKP after 28 days of curing under ambient conditions and increases their mechanical strength. The oxidation state of Re and the reduction from Re (VII) to Re (IV) was estimated using X-ray-absorption near-edge structure (XANES) analysis. Considering the Re leaching concentrations from tests using the ANS-16.1 standard in water, enhanced leachability indices (LI) for Re from MKP matrices were determined with the addition of iron-bearing fillers. Overall, the average LI values were greater than the minimum limit, indicating their acceptance for disposal recommended by the U.S. Nuclear Regulatory Commission.