It is well known that aqueous solutions can emit electromagnetic waves in the radio frequency range. However, the physical nature of this process is not yet fully understood. In this work, the possible role of gas nanobubbles formed in the bulk liquid is considered. We develop a theoretical model based on the concept of gas bubbles stabilized by ions, or “bubstons”. The role of bicarbonate and hydronium ions in the formation and stabilization of bubstons is explained through the use of quantum chemical simulations. A new model of oscillating bubstons, which takes into account the double electric layer formed around their gas core, is proposed. Theoretical estimates of the frequencies and intensities of oscillations of such compound species are obtained. It was determined that oscillations of negatively charged bubstons can occur in the GHz frequency range, and should be accompanied by the emission of electromagnetic waves. To validate the theoretical assumptions, we used dynamic light scattering (DLS) and showed that, after subjecting aqueous solutions to vigorous shaking with a force of 4 or 8 N (kg·m/s²) and a frequency of 4–5 Hz, the volume number density of bubstons increased by about two orders of magnitude. Radiometric measurements in the frequency range of 50 MHz to 3.5 GHz revealed an increase in the intensity of radiation emitted by water samples upon the vibrational treatment. It is argued that, according to our new theoretical model, this radiation can be caused by oscillating bubstons.

The advancement of experimental methods has provided new information about the structure and structural fluctuations of water. Despite the appearance of numerous models, which aim to describe a wide range of thermodynamic and electrical characteristics of water, there is a deficit in systemic understanding of structuring in aqueous solutions. A particular challenge is the fact that even pure water is a heterogeneous, multicomponent system composed of molecular and supramolecular structures. The possibility of the existence of such structures and their nature are of fundamental importance for various fields of science. However, great difficulties arise in modeling relatively large supramolecular structures (e.g. extended hydration shells), where the bonds between molecules are characterized by low energy. Generally, such structures may be non-equilibrium but relatively long-lived. Evidently, the short times of water microstructure exchanges do not mean short lifetimes of macrostructures, just as the instability of individual parts does not mean the instability of the entire structure. To explain this paradox, we review the data from experimental and theoretical research. Today, only some of the experimental results on the lifetime of water structures have been confirmed by modeling, so there is not a complete theoretical picture of the structure of water yet. We propose a new hierarchical water macrostructure model to resolve the issue of the stability of water structures. In this model, the structure of water is presented as consisting of many hierarchically related levels (the stratification model). The stratification mechanism is associated with symmetry breaking at the formation of the next level, even with minimal changes in the properties of the previous level. Such a hierarchical relationship can determine the unique physico-chemical properties of water systems and, in the future, provide a complete description of them.

Electrons localized by water molecules are known as hydrated electrons. The composition of the aqueous environment determines their state and behavior. In this experimental and theoretical work, hydrated electrons were formed in aqueous solutions upon high-energy electron impact, and the dependence of their characteristics on the presence of nanobubbles generated during vibrational treatment was investigated. To explain the results, quantum chemical simulations were carried out, and diverse possible kinetic schemes were considered. Absorbance of deionized water and NaCl aqueous solution was measured at a wavelength of 600 nm, which falls in the range typical of hydrated electrons. The principal differences in the spectral responses of the samples were discovered depending on whether they were preliminarily subjected to repeated vigorous shaking or not. Vigorous shaking caused a noticeable increase in both the integral and maximum absorbance, and the absorbance decay was significantly slower. The effects observed in the vibrationally treated aqueous samples were found to be explained only in the framework of a kinetic scheme that assumes the repeated solvation of electrons, which are transferred from a localized to a delocalized (free) state upon the energy absorption. This repeated solvation is possible only when the secondary electrons are localized on the inner surfaces of the boundary hydration shells of nanobubbles, which are formed in the process of shaking. Thus, nanobubbles substantially change the apparent gross lifetime and properties of hydrated electrons, and these changes, in turn, can indicate the presence of nanobubbles in water and aqueous solutions.

A comparative study of the properties of cytochrome c in its interaction with phosphatidic acid is carried out. Similar conformational changes in the active center of cytochrome c occurring during its interaction with both cardiolipin and phosphatidic acid are demonstrated using the methods of spectrofluorometry. The presence of similar magnitudes of peroxidase activity of cytochrome c in its interaction with both cardiolipin and phosphatidic acid was corroborated by luminol-dependent chemiluminescence, and the use of the EPR method enabled the detection formation of phenoxyl radical of etoposide in both complexes. It can be concluded that both phosphatidic acid and cardiolipin effectively alter the structure of the active center of cytochrome c and contribute to the enhancement of its peroxidase activity. The obtained results may indicate a very probable participation of both cardiolipin and phosphatidic acid in the development of cytochrome c–mediated proapoptotic processes in mitochondria.