Temperature and concentration dependence of equivalent conductivity in Ca(NO3)2-CaI2-H2O system

1980 ◽  
Vol 45 (6) ◽  
pp. 1639-1645 ◽  
Author(s):  
Jindřich Novák ◽  
Ivo Sláma
Keyword(s):  
Linear Function ◽  
Concentration Dependence ◽  
Mole Fraction ◽  
Constant Temperature ◽  
Salt Concentration ◽  
Free Water ◽  
Water Molecules ◽  
Equivalent Conductivity ◽  
Calcium Salts ◽  
Fraction I

The dependence of the equivalent conductivity on the temperature and composition of the Ca(NO3)2-CaI2-H2O system was studied. The ionic fraction [I-]/([I-] + [NO-3]) was changed from 0.1 to 0.5, the mole fraction of calcium salts (assumed in anhydrous form in the presence of free water molecules) was 0.075-0.200. The equivalent conductivity was found to be a linear function of the ionic fraction at constant temperature and salt concentration.

A discussion on equations of phase equilibrium between two regular binary phases

1981 ◽  
Vol 46 (6) ◽  
pp. 1433-1438
Author(s):  
Jan Vřešťál
Keyword(s):  
Phase Equilibrium ◽  
Linear Function ◽  
Concentration Dependence ◽  
Absolute Temperature ◽  
Enthalpy Change ◽  
Independent Parameter ◽  
Free Enthalpy ◽  
Regular Solutions ◽  
Regular Model ◽  
Concentration Dependences

The conditions of the existence of extreme on the concentration dependences of absolute temperature (x are mole fractions) T = Tα(xkα) and T = Tβ(xkβ) denoting equilibrium between two binary regular solutions are generally developed under two assumptions: 1) Free enthalpy change of pure components k = i, j at transition from phase α to β is a linear function of temperature. 2) Concentration dependence of excess free enthalpy (identical with enthalpy) of solutions α and β, respectively, is described in regular model by one concentration and temperature independent parameter for each individual phase.

scholarly journals Synthesis, Single Crystal Structural Investigation, Hirshfeld Surface Analysis, Thermoanalysis and Spectroscopic Study of Two New Cu(II) and Co(II) Transition-Metal Complexes

Crystals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 986
Author(s):  
Rim Boubakri ◽  
Mirosław Szybowicz ◽  
Mariola Sadej ◽  
Sarra Soudani ◽  
Frédéric Lefebvre ◽  
...  
Keyword(s):  
Hydrogen Bonds ◽  
Single Crystal ◽  
Organic Ligand ◽  
Free Water ◽  
Pyrimidine Ring ◽  
Water Molecules ◽  
Absorption Bands ◽  
Infrared And Raman Spectroscopy ◽  
Homo And Lumo ◽  
Coordinated Water

Two new complexes, [Cu(dimpyr)2(H2O)2](NO3)2.2H2O (1) and (Hamdimpy)2[CoCl4].H2O (2), with the monodentate ligand 2-amino-6-methylpyrimidin-4-(1H)-one (dimpyr) and the countercation 4-amino-2,6-dimetylpyrimidium (Hamdimpy), respectively, were prepared and characterized by single crystal X-ray diffraction, elemental analysis and IR spectroscopy. In (1), the Cu(II) cation is tetracoordinated, in a square plan fashion, by two nitrogen atoms from the pyrimidine ring of the organic ligand and two oxygen atoms of two coordinated water molecules. In the atomic arrangement, the CuO2N2 square planes are interconnected via the formation of O-H…O hydrogen bonds involving both coordinated and free water molecules and NO3− nitrate anions to form inorganic layers parallel to the (a, b) plane at z = (2n + 1)/4. In (2), the central atom Co(II) is four-coordinated in a distorted tetrahedral fashion by four Cl− ions. The [CoCl4]2− tetrahedra are arranged parallel to the plane (110) at x = (2n + 1)/2 and the organic cations are grafted between them by establishing with them hydrogen bonds of CH…Cl and NH…Cl types. The vibrational absorption bands were identified by infrared and Raman spectroscopy. Intermolecular interactions were investigated via Hirshfeld surfaces and electronic properties such as HOMO and LUMO energies were derived. The two compounds were characterized by thermal analysis to determine their thermal behavior with respect to temperature.

scholarly journals Single and multiple excitations in double-core-hole states of free water molecules

2020 ◽  
Vol 53 (22) ◽  
pp. 224002
Author(s):  
T Marchenko ◽  
S Carniato ◽  
G Goldsztejn ◽  
O Travnikova ◽  
L Journel ◽  
...  
Keyword(s):  
Free Water ◽  
Water Molecules ◽  
Core Hole

scholarly journals DSC reveals variation in enthalpy associated with free water molecules in water-ethanol solution exposed to x-rays and magnetic field

2021 ◽  
Vol 17 (1) ◽  
pp. 07-07
Author(s):  
Nirmal Chandra Sukul ◽  
Tandra Sarkar ◽  
Atheni Konar ◽  
Md. Amir Sohel ◽  
Asmita Sengupta ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Aqueous Ethanol ◽  
Free Water ◽  
Ethanol Solution ◽  
Water Molecules ◽  
X Rays ◽  
Standard Medium ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Homeopathic Drugs

Aqueous ethanol is the standard medium for all drugs used in homeopathy. X-ray and Magnetispoli ambo are 2 homeopathic drugs prepared by exposure of aqueous ethanol to x-rays and static magnetic field, respectively.Mother tinctures (MT)weresuccessively diluted with solvent 1:100 and succussed in several steps to prepare centesimal potencies 8 cH, 14 cH and 32 cH. The solvent was processed in the same way. Although identical in chemical composition (0.03 molar ethanol) and water content (96%) these preparations like the Mother tinctures and three potencies of X-ray and Magnetispoli amboexhibit different therapeutic pathological effects. Potency 8cH of each preparation was diluted with water to reach concentrations 4%, 20%, 40% and 80% ethanol. The aim of the study was to establish whether these potencies exhibited variation in free water molecules. Differential Scanning Calorimetry (DSC) of MT and potencies exhibited almost similar freezing and melting points, but they remarkably differed in freezing and melting enthalpy and free water molecules. The various dilutions of potency 8cH exhibited variation in enthalpies and free water molecules, being this variation independent of the amount of water added. We conclude that exposure of aqueous ethanol to x-rays and magnetic field, with subsequent dilution and agitation induces changes in the solvent involving free water molecules. All X-ray and Magnetispoli ambo potencies were analyzed by means of Raman spectroscopy for free water molecules. The results were compared to the ones of DSC, being more or less similar.

scholarly journals Water Adsorption to Leaves of Tall Cryptomeria japonica Tree Analyzed by Infrared Spectroscopy under Relative Humidity Control

Plants ◽  
2020 ◽  
Vol 9 (9) ◽  
pp. 1107
Author(s):  
Wakana A. Azuma ◽  
Satoru Nakashima ◽  
Eri Yamakita ◽  
Tamihisa Ohta
Keyword(s):  
Hydrogen Bonding ◽  
Relative Humidity ◽  
Cryptomeria Japonica ◽  
Water Adsorption ◽  
Bound Water ◽  
Free Water ◽  
High Water ◽  
Water Molecules ◽  
Cross Sectional ◽  
Tissue Properties

Leaf water storage is a complex interaction between live tissue properties (anatomy and physiology) and physicochemical properties of biomolecules and water. How leaves adsorb water molecules based on interactions between biomolecules and water, including hydrogen bonding, challenges our understanding of hydraulic acclimation in tall trees where leaves are exposed to more water stress. Here, we used infrared (IR) microspectroscopy with changing relative humidity (RH) on leaves of tall Cryptomeria japonica trees. OH band areas correlating with water content were larger for treetop (52 m) than for lower-crown (19 m) leaves, regardless of relative humidity (RH). This high water adsorption in treetop leaves was not explained by polysaccharides such as Ca-bridged pectin, but could be attributed to the greater cross-sectional area of the transfusion tissue. In both treetop and lower-crown leaves, the band areas of long (free water: around 3550 cm−1) and short (bound water: around 3200 cm−1) hydrogen bonding OH components showed similar increases with increasing RH, while the band area of free water was larger at the treetop leaves regardless of RH. Free water molecules with longer H bonds were considered to be adsorbed loosely to hydrophobic CH surfaces of polysaccharides in the leaf-cross sections.

c , T-Dependence of the Self Diffusion in Concentrated Aqueous Sucrose Solutions

1994 ◽  
Vol 49 (3-4) ◽  
pp. 258-264 ◽  
Author(s):  
D. Girlich ◽  
H.-D. Lüdemann ◽  
C. Buttersack ◽  
K. Buchholz
Keyword(s):  
Field Gradient ◽  
Concentration Dependence ◽  
Diffusion Coefficients ◽  
The Self ◽  
Water Molecules ◽  
Pulsed Field Gradient Nmr ◽  
Pulsed Field ◽  
Self Diffusion ◽  
Sucrose Solutions ◽  
Wide Range

The self diffusion coefficients D of the water molecules and of sucrose have been determined by the pulsed field gradient NMR technique over a wide range of temperatures and concentrations (cmax: 70% w/w suc.). All temperature dependencies can be fitted to a Vogel- Tammann-Fulcher equation. The isothermic concentration dependence of D for the sucrose is given by a simple exponential concentration dependence

Fractionation of Hydrogen Isotopes in Aqueous Lithium Chloride Solutions

1988 ◽  
Vol 43 (5) ◽  
pp. 449-453 ◽  
Author(s):  
Masahisa Kakiuchi
Keyword(s):  
Oxygen Isotope ◽  
Isotope Effect ◽  
Lithium Chloride ◽  
Structural Changes ◽  
Platinum Catalyst ◽  
Pure Water ◽  
Free Water ◽  
Hydrogen Gas ◽  
Water Molecules ◽  
Chloride Solutions

The D/H ratio of hydrogen gas in equilibrium with water vapor over aqueous lithium chloride solutions was measured at 25 °C, using a hydrophobic platinum catalyst. Experimental details are described. The hydrogen isotope effect between the solution and pure water depends linearly on the LiCl concentration up to ca. 12 m, and at higher concentrations a marked deviation from linearity takes place, as was also observed for the oxygen isotope effect measured by Bopp et al. On the basis of these hydrogen and oxygen isotope effects it is concluded that H218O is enriched in the water molecules coordinated to Li+ ions and HD16O is enriched in the free water molecules of the solution. The observed deviation from linearity for concentrations higher than ca. 12m is interpreted in terms of structural changes in the hydration sphere of the Li+ ions.

Hydrogen Isotope Fractionation in Aqueous Alkali Halide Solutions

1997 ◽  
Vol 52 (11) ◽  
pp. 811-820 ◽  
Author(s):  
Masahisa Kakiuchi
Keyword(s):  
Oxygen Isotope ◽  
Isotope Effect ◽  
Alkali Halide ◽  
Hydrogen Isotope ◽  
Isotope Fractionation ◽  
Free Water ◽  
Aqueous Alkali ◽  
Water Molecules ◽  
Oxygen Isotope Fractionation ◽  
Hydrogen Isotope Effect

Abstract The D/H ratios of hydrogen gas in equilibrium with aqueous alkali halide solutions were deter-mined at 25 °C, using a hydrophobic platinum catalyst. The hydrogen isotope effect between the solution and pure water changes linearly with the molality of the solution at low concentrations, but deviates from this linearity at higher concentration for all alkali halide solutions. The magnitude of the hydrogen isotope effect is in the order; Kl > Nal > KBr > CsCl ≧ NaBr > KCl > NaCl > LiCl, at concentrations up to a molality of 4 m. The sign and trend of the hydrogen isotope effect is different from that of oxygen. In aqueous alkali halide solutions, the hydrogen isotope effect is influenced by both the cation and the anion species, while the oxygen isotope effect is mainly caused by the cation species. This suggests that the mechanism of hydrogen isotope fractionation between the water molecules in the hydration spheres and the free water molecules differs from the mechanism of the oxygen isotope fractionation. The hydrogen and oxygen isotope effects for alkali halides, except LiCl and NaCl, may be influenced by changes in energy of the hydrogen bonding in free water molecules.

Sign in / Sign up

Export Citation Format

Share Document