V. N. Trostin

Concentration dependence of the structure of aqueous solutions of lutetium nitrate according to X-ray diffraction

Aqueous solutions of lutetium nitrate over a wide range of concentrations are studied by X-ray diffraction under standard temperature and pressure. The low-angle peaks in experimental scattering intensity curves are interpreted. It is shown that the structure of these solutions can be of two types. It is found that a saturated solution and solutions concentrated to a molar ratio of 1: 20 have a quasi-crystalline structure resulting from interionic interactions. It is determined that dilute solutions form a water-like structure characterized by a tetrahedral network of hydrogen bonds between the water molecules. It is found that low-angle peaks also appear in the intensity curves of dilute solutions; this proves that the so-called “long-range” order is preserved in these solutions. It is revealed that in all the studied systems, the contributions to the total scattering pattern that are responsible for the occurrence of pre-peaks are intercationic interactions.

An X-ray diffraction study of aqueous solutions of lutetium trichloride

The X-ray diffraction analysis is used to study aqueous solutions of lutetium chloride in a wide concentration range under standard conditions. Small angle peaks on the functions of the X-ray scattering intensity and the maxima of radial distribution functions of the atomic-electron density are interpreted. It is found that highly concentrated solutions are characterized by a unique quasi-crystalline structure distinguished by short- and long-range ordering. Dilution of solutions results in that the own structure of the solvent starts to play the major role in the structure of the systems. It is established for the first time that small angle peaks on the scattering intensity functions are also manifested for diluted solutions, which indicates that long-range ordering is preserved in them.

Chemolysis of calcium oxalate stones: study in vitro and possible clinical application

The flow cell modeling clinical conditions have been used to study the interaction between dilute chemolytic solutions and large calcium oxalate renal stones. The stone treatment with 5% disodium ethylenediaminetetraacetate aqueous solutions or citrate buffer are found not to provide notable disruption of the samples studied. The significant improvement is reached with the mixed compositions containing both natural and synthetic chelating reagents:citrate and ethylenediaminetetraacetate ions as well as an antibiotic. Description of the chemolytic irrigation, numerical results and their possible clinical application are the main topic of the present research.

Concentration dependence of the structure of aqueous solutions of samarium trichloride according to X-ray diffraction

Aqueous solutions of samarium chloride in a wide range of concentration under ambient conditions are studied by X-ray diffraction analysis. The small-angle peaks in experimental scattering intensity curves are interpreted. It is shown that highly concentrated solutions are characterized by a unique structure that differs heavily from the structure of dilute systems. It is found that small-angle peaks also appear in the intensity curves of dilute solutions, indicating that the so-called long-range order is preserved in these solutions. It is revealed that the contributions to the total scattering pattern that govern the appearance of prepeaks are interionic interactions of different types (e.g., cation-cation, anion-cation, and anion-anion interactions) in concentrated systems and the distances between the cations in dilute solutions.

Effect of concentration on the structure of aqueous solutions of gadolinium chloride and gadolinium nitrate as probed by X-ray diffraction

Aqueous solutions of gadolinium chloride and gadolinium nitrate are studied by X-ray diffraction over wide ranges of concentrations under standard temperature and pressure. Small-angle peaks on measured scattering intensity curves are interpreted. Small-angle peaks are found not only on the intensity curves for concentrated solutions, but also on those for dilute systems, and this proves that these systems retain a long-range order. Diverse types of ion-ion interactions are shown to be the major contributors to the overall scattering pattern that are responsible for the appearance of pre-peaks.

Polymorphic conversions of 4-tert-butylcalix[4]arene upon the formation and thermal destruction of a complex with n-hexane

Complex polymorphic conversions of 4-tert-butylcalix[4]arene upon the formation and thermal destruction of a complex with n-hexane were revealed by combined analysis of powder X-ray pictures and data obtained by differential scanning calorimetry.

Polymorphism of 4-tert-butylcalix[4]arene upon the formation and thermal destruction of its complex with acetonitrile

It is demonstrated that combined analysis of powder X-ray diagrams and differential scanning calorimetry allows us to reveal complex polymorphic transformations of 4-tert-butylcalix[4]arene upon the formation and thermal destruction of its complex with acetonitrile. The stability of 4-tert-butylcalix[4]arene polymorph containing no solvent molecules in the crystal lattice after the removal of acetonitrile is assumed.

Enthalpies of reaction of calcium chloride and sodium oxalate in aqueous solution of Tween 80

The heats of mixing of dilute calcium chloride and sodium oxalate solutions in water and aqueous solutions of a nonionogenic surfactant, namely, polyoxyethylene (20) sorbitan monooleate (Tween 80) containing 1–5 wt % of the dissolved substance were measured at 298.15 K. The heats of dilution of calcium chloride solutions were determined, and the enthalpies of precipitation of calcium oxalate in water and surfactant solutions were calculated. The surfactant concentration was found to have almost no effect on the enthalpies of the processes under study; rather, it modifies the shape of the resultant deposit by preventing the agglomeration of calcium oxalate particles.

The enthalpies of interactions of Ca2+(aq) and C2O42− (aq) ions in complexon solutions: Competition between complexation and precipitation

The thermal effects of mixing of aqueous calcium chloride with sodium citrate and ethylenedi-aminetetraacetate in the absence and presence of sodium oxalate have been measured at 25°C. The thermal effects of dilution of aqueous calcium chloride solutions were determined. The thermal effects of calcium oxalate precipitation and formation of calcium complexes with citrate and ethylenediaminetetraacetate ions were calculated. The 1% solution of sodium citrate inhibited the formation of CaC2O4 (s); in a 1% solution of sodium ethylenediaminetetraacetate with [Ca2+][C2O42−] > 10−5, the endothermal formation of the [CaEdta]2− complex quickly changed to exothermal precipitation. The 3 and 5% solutions of complexons showed a pronounced inhibiting effect on the formation of urinary stones even when the concentration of calcium and oxalate ions in solution exceeded the product of solubility of CaC2O4 by four and more orders of magnitude.

The Complexon-Renal Stone Interaction: Solubility and Electronic Microscopy Studies

We have studied how complex formation between calcium and ethylenediaminetetraacetate or citrate ions influences the surface texture and the size of passed oxalate-phosphate renal stones. The four hour concrement treatment by sodium citrate or ethylenediaminetetraacetate aqueous solutions strongly affects the stone texture and provides a mass loss of 6-15%. We have found a significant decrease of the calcium and phosphor content on a concrement surface and formation of appreciable cracks. Our results do indicate that the Ca-complexon interaction can be effectively applied for disrupting some types of renal stones and, especially, residual concrements, which frequently occurs after a surgical operation or an extracorporeal shock-wave lithotripsy. This study provides an additional quantitative physicochemical basis for this slightly invasive therapy.