Decomposition in Prolonged Storage of KF · H<Subscript>2</Subscript>O<Subscript>2</Subscript> Stabilized with Carboxylic Acids

Decomposition of KF · H₂O₂ stabilized with carboxylic acids (maleic, fumaric, succinic, adipic) in storage for more than three years at 20°C was studied. Rate constants of decomposition of stabilized KF · H₂O₂ were determined in different time intervals. The chemical reactions in the system KF-H₂O₂-carboxylic acid in the stage of preparation of solid KF · H₂O₂ stabilized with carboxylic acid and those during prolonged storage of the final product are discussed.__________Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 2, 2005, pp. 287–291.Original Russian Text Copyright © 2005 by Titova, Nikol’skaya, Buyanov, Pudova, Karzhavina.     

An open-shell INDO study of models for the stabilized O− ion in γ-irradiated alkaline ices

Structural models for stabilized O^– in -irradiated alkaline ices are evaluated. INDO calculations on hydrated O^– indicate octahedral coordination and hydrogen bond orientations for the water molecules are preferred. INDO results for hydrated OH^– are compared with crystallographic data for NaOH hydrates: a scaling factor for calculated hydrogen bond lengths is developed and applied to hydrogen bonded O^– models. The hydrated O^– model is closely similar to the hydrated anions in KF · 4H₂O, NaOH · 4H₂O, and NaOH · 7H₂O. A second model is developed, involving H₃O⁺ along with H₂O, in the O^– stabilization shell. Both models are discussed in terms of alkaline ice radiation chemistry.     

Thermal stability and crystal structure of potassium fluoride monoperoxosolvate KF·H2O2

Potassium fluoride peroxosolvate KF-H₂O₂ was obtained upon action of a 30% aqueous solution of hydrogen peroxide on solid potassium fluoride dihydrate. As compared to other peroxosolvates, KF-H₂O₂ is characterized by the highest thermal stability: the decomposition rate constantk ₁, at 120°C is 1.4 10^–3 min^–1, the enthalpy of H₂O₂ addition to KF is 8.1 kcal/ mol. The correlation between the high stability of KF-H₂O₂ and the absence of catalytic properties of KF towards H₂O₂, and the formation of strong intermolecular O-H...F and intramolecular O-H...O hydrogen bonds in the crystal is discussed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 38–44, January, 1993.     

Studies on synthesis, characterization and thermochemistry of Mg2[B2O4(OH)2]·H2O

A new magnesium borate Mg₂[B₂O₄(OH)₂]·H₂O has been synthesized by the method of phase transformation of double salt at hydrothermal condition and characterized by XRD, IR, TG and DSC. The enthalpy of solution of Mg₂[B₂O₄(OH)₂]·H₂O in 0.9764 mol L^–1 HCl was determined. With the incorporation of the enthalpies of solution of H₃BO₃ in HCl (aq), of MgO in (HCl+H₃BO₃) (aq), and the standard molar enthalpies of formation of MgO(s), H₃BO₃(s), and H₂O(l), the standard molar enthalpy of formation of –(3185.78±1.91) kJ mol^–1 of Mg₂[B₂O₄(OH)₂]·H₂O was obtained.This revised version was published online in November 2005 with corrections to the Cover Date.     

NH4F·H2O2, a new peroxyhydrate

Conclusions The new molecular compound NH₄F·H₂O₂ was observed during an investigation of the fusibility of the NH₄F-H₂O₂-H₂O system and has been isolated.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1617–1618, July, 1968.     

The synthesis and properties of zeolite CF-3

The novel zeolite CF-3, with a high ratio of SiO₂/Al₂O₃ and a characteristic X-ray powder diffraction pattern, has been synthesized hydrothermally from a TMEDA-Na₂O–SiO₂–Al₂O₃–H₂O system at 200°C. The molar composition of CF-3 is (0.4–0.6)Na₂O·(1.5–6.3)TMEDA·Al₂O₃·(80–400)SiO₂·(0–17)H₂O·CF-3 is similar to ZSM-39 and melanophlogite, which have a clathrate-type structure.     

Detection of HO2 radicals during decomposition of K2CO3·3H2O2

Conclusions HO₂ radicals were detected in the partial decomposition product of K₂CO₃·3H₂O₂ by the EPR method.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1638–1639, July, 1973.     

Gas-Sensing Properties of Doped In2O3 Films as Sensors for NO2 in Air

A number of sensing systems based on indium oxide doped with various metal oxides (In₂O₃ · WO₃, In₂O₃ · ZnO, In₂O₃ · RuO₂, In₂O₃ · Gd₂O₃, and In₂O₃ · Sm₂O₃) in amounts of no more than 3–5 mol % and also Au · In₂O₃ films were studied as sensors for detecting NO₂ in air. The working temperature of sensors was 250°C (except for In₂O₃ · RuO₂, for which T = 150–190°C). In₂O₃ · WO₃-based sensors reach a high sensitivity especially at a concentration of NO₂ in air higher than 10 ppm (the relative sensor conductivity changes by 2.5 orders of magnitude). However, a shortcoming of this system is an increased response time (7–9 min) as compared to the other studied systems, for which the response time does not exceed 15–20 s. In₂O₃ · Gd₂O₃ and In₂O₃ · Sm₂O₃ films exhibit the best sensing properties in sensitivity, selectivity, and stability. Various NO₂ species adsorbed on the surface of dispersed indium oxide were detected by Fourier-transform IR spectroscopy. The mechanism of changing the conductivity of In₂O₃ · Gd₂O₃ films upon detecting NO₂ in air is discussed.     

Thermochemical properties of potassium fluoride peroxohydrates

Conclusions The heats of dissolution of hydrogen peroxide in water have been measured, and on the basis of this we have calculated the standard enthalpies of formation of KF and KF·nH₂O₂ (where n=1–3). We have also calculated the enthalpy of the combination of H₂O₂ to KF_cr.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 247–250, February, 1989.     

Infrared spectra (700–200 cm−1) and6Li/7Li and H2O/D2O isotope effects for four isotopically substituted lithium formate monohydrates

The infrared spectra, in the 700–200 cm^–1 region, have been reported for⁶LiHCO₂ · H₂O,⁶LiHCO₂ · D₂O,⁷LiHCO₂ · H₂O and⁷LiHCO₂ · D₂O and the observed fundamental bands have been discussed taking into account the⁶Li/⁷Li and H₂O/D₂O isotope wavenumber shifts on the fundamental vibrations.

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Infrarotspektren (700–200 cm^–1) und⁶Li/⁷Li- und H₂O/D₂O-Isotopeneffekte für vier isotopensubstituierte Lithiumformat-monohydrate

Zusammenfassung Die Infrarotspektren in der Region von 700–200 cm^–1 werden für⁶LiHCO₂ · H₂O,⁶LiHCO₂ · D₂O,⁷LiHCO₂ · H₂O und⁷LiHCO₂ · D₂O angegeben und die beobachteten Grundschwingungen zusammen mit den isotopischen Verschiebungen der Wellenzahlen diskutiert.

     

Diagramme polythermique du systeme ternaire H2O—Al(NO3)3—Mg(NO3)2

The solid—liquid equilibria of the ternary system H₂O—Al(NO₃)₃—Mg(NO₃)₂ were studied at –30, –20, –10 and 0°C by using a synthetic method which allows to detemine all the characteristic points of isothermal sections. The stable solid phases which appear are respectively: ice, Al(NO₃)₃·9H₂O, Mg(NO₃)₂·9H₂O and Mg(NO₃)₂·6H₂O. Neither double salts nor mixed crystals are observed in the temperature and composition field studied. Polytherm diagram layout show two invariant transformations correspond with an eutectic point and a peritectic point.This revised version was published online in November 2005 with corrections to the Cover Date.     

A study by pulse radiolysis of the radiation-chemical transformation of aqueous solutions of hydrazine in the presence of oxygen

It is shown by pulse radiolysis that in aqueous solutions of hydrazine containing oxygen the radical N₂H₃ reduces oxygen to O₂ ^– at pH > 7 (k 3·10⁹ dm³· mole^–1·sec^–1), while this reaction does not occur for the protonated form N₂H₄ ⁺ at pH < 7 (k, 5·10⁶ dm³·mole^–1·sec^–1). The rate constants for the disappearance of O₂ ^– have been determined in the pH range from 4 to 12. Rate constants have been calculated for the reaction of O^– with N₂H₄ [k=(1.6 ±0.2)·10⁹ dm³·mole^–1·sec^–1] and of O₃with N₂H₄ [k=(1.2 ±0.2)·10⁶ dm³· mole^–1·sec^–1].Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 341–345, February, 1991.     

By-product formation in spark breakdown of SF6/O2 mixtures

The yields of SOF₄, SO₂F₂, SOF₂, and SO₂ have been measured as a function of O₂ content in SF₆/O₂ mixtures, following spark discharges. All experiments were made at a spark energy of 8.7 J/spark, a total pressure of 133 kPa, and for O₂ additions of 0, 1, 2, 5, 10, and 20% to SF₆. Even for the case of no added O₂, trace amounts of O₂ and H₂O result in the formation of the above by-products. However, addition of O₂ significantly increases the yields of SOF₄ and SO₂F₂, while SOF₂ is only slightly affected. The net yields for SOF₄ and SO₂F₂ formation range from 0.18×10^–9 and 0.64×10^–10 mol·J^–1, respectively, at 1% O₂ content to 10.45×10^–9 and 7.15×10^–10 mol·J^–1, respectively, at 20% O₂ content. The mechanism for SOF₄ production appears to involve SF₄, an important initial product of SF₆, as a precursor. Comparison of the SOF₄ and SO₂F₂ yield from spark discharges (arc and corona) shows that the yields from other discharges (arc and corona) shows that the yields can vary by at least three orders of magnitude, depending on the type of discharge and on other discharge parameters.     

Redox Equilibria in the System Fe(OH)3(H2SO4)-Na2SO3-H2O Involving Precipitation of Iron(II) Sulfite as a Fe2O3 Precursor

Experimental data on the equilibria Fe²⁺/Fe³⁺ and SO₃ ²⁻/SO₄ ²⁻ in the system Fe(OH)₃(H₂SO₄)-Na₂SO₃-H₂O are presented. The quantitative relations between the reduction of Fe(III) and the precipitation of FeSO₃·2.5H₂O as a Fe₂O₃ precursor have considered graphically.__________Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 1, 2005, pp. 41–44.Original Russian Text Copyright © 2005 by Vasekha, Motov.     

IR-Spektralanalyse von Gläsern des Systems TeO2−V2O5

Studies of glasses and their crystalline products in the TeO₂–V₂O₅ system were made in the 1400–400 cm^–1 range. A continuous shift of the V=O-band from 1020 cm^–1 to 940 cm^–1 was found in the glasses with decreasing concentration of V₂O₅, as well as a sharp decrease in the intensity at 830 cm^–1. On the basis of the results obtained, it is concluded that with increasing TeO₂ content, the structure of the glasses is changed, caused by the breaking of the V–O–V bonds and the formation of Te–O–Te bridges.The IR-spectrum of the 2TeO₂·V₂O₅ compound in both crystalline and vitreous states was studied for the first time. The behaviour of the absorption bands is related to the structure of the glasses studied.

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Mit 4 Abbildungen     

Solubility in the systems Rb2SO4-H2SO4-H2O and Cs2SO4-H2SO4-H2O at 25°

Conclusions The solubility of rubidium and cesium sulfates in aqueous solutions of sulfuric acid was studied at 25°. Rubidium sulfate forms the compounds 3Rb₂SO₄· H₂SO₄, Rb₂SO₄ · H₂SO₄, Rb₂SO₄·3H₂SO₄ and Rb₂SO₄·7H₂SO₄ with sulfuric acid, while cesium sulfate forms the compounds Cs₂SO₄·H₂SO₄; Cs₂SO₄·3H₂SO₄ and Cs₂SO₄ · 7H₂SO₄.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1166–1170, June, 1968.     

Formation Mechanism of O2– Radical Anions in the Adsorption of NO + O2 and NO2 + O2 Mixtures on ZrO2 According to EPR and TPD Data

The effects of various factors on the formation of O₂ ^– radical anions in the adsorption of an NO + O₂ or NO₂ + O₂ mixture on ZrO₂ were studied. It was found that the thermal stability of the O₂ ^– species depends on the composition of the adsorbed gas. It was suggested that nitrogen oxide complexes on ZrO₂ centers are responsible for the formation of O₂ ^–. These centers are formed upon the treatment of the oxide in a vacuum; however, they are different from both coordinatively unsaturated Zr⁴⁺ cations (NO adsorption centers at 77 K) and Zr⁴⁺–O^––O^––Zr⁴⁺ centers, at which O₂ ^– are formed because of the adsorption of H₂ + O₂. Based on the experimental data, the mechanism of O₂ ^– formation in the adsorption of an NO + O₂ mixture is discussed.     

Peroxyhydrates of rubidium and cesium fluorides

Conclusions The compounds RbF · H₂O₂, RbF · 2H₂O₂, and CsF · H₂O₂ have been synthesized for the first time, and their thermal stabilities were investigated.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1871–1873, August, 1972.     

SCF LCAO MO studies on the hydration of ions: The system F− · 2H2O

The energy surface of the dihydrated fluoride anion (F·2H₂O)^–1 is studied for a number of different geometry points near the equilibrium structure within the SCF LCAO MO framework, using an extended gaussian basis set to approximate the molecular wavefunctions. For the first and second hydration step of the fluoride anion the corresponding hydration energies are calculated to beB ₁ ^scf =24.1 kcal/mole andB ₂ ^SCF =20.8 kcal/mole (experimental measurements: 23.3 kcal/mole and 16.6 kcal/mole, respectively). The hydration energies and equilibrium bond distances obtained for the dihydrated fluoride anion (F·2H₂O)^– are compared with those found for the monohydrate (FHOH)^– and with corresponding results of the dihydrated lithium cation (Li · 2H₂O)⁺. The system (F·2H₂O)^– is taken as a very simple model to discuss some basic features of the hydration process of small ions and to study the influence of a negative ion on an adjacent hydrogen bond.We would like to thank our technical staff for valuable help in carrying out these calculations.     

Formation of gels and gel-glasses in the VO2(V2O5)-SiO2 systems

Blue-coloured gels have been prepared in the VO₂-SiO₂ system up to 80 mol% VO₂ by sol-gel technology using TEOS and aqueous solutions of VOSO₄·5H₂O. It is established by means of VIS and ESR spectra that at low temperatures VO²⁺ complexes are formed. An oxidation of V⁴⁺ has taken place with increasing temperature, and V₂O₅ and cristobalite have been separated. Silica gel glasses stable up to 800°C have been obtained from gels containing 1–3 mol% VO₂.