Temperature dependence of protonic conductivity of porous glasses saturated with solutions of cesium dihydroorthophosphate in orthophosphoric acid

Wide-pore-glass plates saturated with solutions of cesium dihydroorthophosphate in orthophosphoric acid demonstrate a monotonic rise in the protonic conductivity in the temperature range 373–523 K, with σ ≥ 10^–2 Ω^–1 cm^–1 reached.     

Temperature dependence of DC electrical conductivity of kaolin

The samples from kaolin Sedlec were investigated by the help of DTA, TG, and temperature dependences of DC conductivity using Pt wire electrodes and linear heating up to 1,050 °C. After drying, the samples contained ~1.5 mass% of the physically bound water. DTA and TG reflected generally known facts about a release of the physically bound water, dehydroxylation, and metakaolinite → Si–Al spinel transformation. The results of electrical measurements showed the electric current passed over the maximum at 60 °C. The self-ionization of water results in the process H₂O → H⁺ + OH^? in the water layers on the crystal surfaces; consequently, OH^? and H⁺ are the main charge carriers in the low-temperature region. The water molecules simultaneously evaporate from the sample which decreases the number of the charge carriers. When the physically bound water evaporates, the current is carried mostly by K⁺ and Na⁺ ions. During dehydroxylation, the hydroxyls OH^? split into H⁺ and O^2?. The ions H⁺ jump to the neighboring OH^? groups creating the water molecules. The ions O^2?remain bounded to the newly created metakaolinite lattice. Therefore, mobile protons contribute to the electric current. At the same time, this contribution gradually decreases because of the escape of H₂O from the sample. The sharp current peak and DTA peak at 970 °C imply relatively fast metakaolinite → Si–Al spinel transformation. This DC current peak results from the shift of Al³⁺ and O^2? ions into new positions.     

Temperature dependence of the electrical conductivity of imidazolium ionic liquids

The electrical conductivities of 1-alkyl-3-methylimidazolium tetrafluoroborate ionic liquids and of 1-hexyl-3-methylimidazolium ionic liquids with different anions were determined in the temperature range between 123 and 393 K on the basis of dielectric measurements in the frequency range from 1 to 10(7) Hz. Most of the ionic liquids form a glass and the conductivity values obey the Vogel-Fulcher-Tammann equation. The glass transition temperatures are increasing with increasing length of the alkyl chain. The fragility is weakly dependent on the alkyl chain length but is highly sensitive to the structure of the anion.     

Formation of copper(II) oxide nanostructures in porous glass as revealed by electrical conductivity measurements

Copper(II) oxide was synthesized in a glass matrix by multiple cycles of impregnation of porous glass with an aqueous solution of copper nitrate, followed by dehydration and thermal decomposition of the salt. The electrical conductivity and its temperature dependences, measured during the progressive accumulation of copper(II) oxide in porous glass, are indicative of a gradual change from chains to 2D structures, eventually resulting in a conductive oxide monolayer.     

Temperature dependence of the electrical conductivity in EMIM-based ionic liquids: Evidence of Vogel–Tamman–Fulcher behavior

We present measurements of the electrical conductivity versus temperature for six pure 1-ethyl-3-methyl imidazolium (EMIM) based ionic liquids (ILs) at atmospheric pressure. The temperature range measured goes from 250 to 430 K, although the exact range for each IL varies depending on its melting and vaporisation temperatures. The data measured shows that the electrical conductivity value for all ILs, except EMIM-BF₄, increases more than 200 times for temperature increases of 180 K. We have also observed that the temperature dependence of the electrical conductivity for all measured ILs can be fitted with high precision with a Vogel–Tamman–Fulcher (VTF) type equation. From the fitting parameters we will extract the activation energy and the glass transition temperature.     

Temperature dependence of the Landau-Placzek ratio in glass forming liquids

Here, we studied Rayleigh-Brillouin light scattering in ten different glass-forming liquids (α-picoline, toluene, o-toluidine, ethanol, salol, glycerol, dibutyl phthalate, o-terphenyl, propylene carbonate, and propylene glycol). For each of these liquids it was found that the Landau-Placzek ratio is in a good agreement with the theory at high temperatures and significantly exceeds the theoretical prediction below a certain temperature. Transition between the two temperature regimes occurs near T(A), where T(A) is crossover point from an Arrhenius-like to a non-Arrhenius behavior for the α-relaxation time dependence on temperature. Increase of the Landau-Placzek ratio relative to the theoretical prediction below T(A) seems to be the universal feature of glass-formers. We suggest that formation of locally favored structures in liquids below T(A) causes observed excess of the Landau-Placzek ratio.     

The electrical conductivity of colloidal tungstic acid

Colloid and Polymer Science - It has been observed that during the dilution of tungstic acid the pH value varies and the variation becomes slow with increasing dilution and after a certain stage it...     

Spin state dependence of electrical conductivity of spin crossover materials

We studied the spin state dependence of the electrical conductivity of the spin crossover compound [Fe(Htrz)(2)(trz)](BF(4)) (Htrz = 1H-1,2,4-triazole) by means of dc electrical measurements. The low spin state is characterized by higher conductance and lower thermal activation energy of the conductivity, when compared to the high spin state.     

Temperature effect on the adsorption and desorption processes in retinoic acid crystals: An electrical conductivity study

Using electrical conductivity as a probe, the effect of crystal temperature on the process of adsorption and desorption of some chemical vapours on retinoic acid semiconductor has been investigated. It has been observed that a three-stage adsorption process in a sample at low temperature changes over to a two-stage process at higher temperature. Measures of activation energies of adsorption and desorption at different stages have been estimated from kinetic data analysis by using a modified Roginsky-Zeldovich equation.     

The Instability of Permanganate in orthophosphoric acid

Solutions of potassium permanganate in concentrated phosphoric acid (above 50%) are found to be unstable. The oxidation state of manganese is reduced from (VII) to (III) and oxygen is evolved during this process. The extent of decomposition of permanganate is found to be dependent on the concentration of the acid.     

Temperature dependence of direct current conductivity in Ag-ED20 nanocomposite films

Russian Journal of Physical Chemistry A - The effect of silver nanoparticles (NPs) in the concentration range of ≤0.8 wt % have on direct current conductivity σdc of Ag-ED20...     

Interaction of basalt with orthophosphoric acid

Physicochemical modeling is used to study the decomposition of basalt by orthophosphoric acid. The equilibrium compositions of the liquid and solid phases of the Al-Fe-Ca-Mg-Na-Si-P-O-H system are calculated. The effects of the acid concentration and solid-to-liquid ratio on the composition of reaction products and the degrees of extraction of iron, aluminum, magnesium, calcium, sodium, and silicon into solution are determined. Conditions for selective extraction of the components into liquid phase are estimated.     

Correlation between molecular orbitals and doping dependence of the electrical conductivity in electron-doped metal-phthalocyanine compounds

We have performed a comparative study of the electronic properties of six different electron-doped metal-phthalocyanine (MPc) compounds (ZnPc, CuPc, NiPc, CoPc, FePc, and MnPc), in which the electron density is controlled by means of potassium intercalation. Despite the complexity of these systems, we find that the nature of the underlying molecular orbitals produces observable effects in the doping dependence of the electrical conductivity of the materials. For all the MPc's in which the added electrons are expected to occupy orbitals centered on the ligands (ZnPc, CuPc, and NiPc), the doping dependence of the conductivity has an essentially identical shape. This shape is different from that observed in MPc materials in which electrons are also added to orbitals centered on the metal atom (CoPc, FePc, and MnPc). The observed relation between the macroscopic electronic properties of the MPc compounds and the properties of the molecular orbitals of the constituent molecules clearly indicates the richness of the alkali-doped metal-phthalocyanines as a model class of compounds for the investigation of the electronic properties of molecular systems.     

Electrical conductivity of porous glasses saturated with sulfuric acid solutions

Electrical conductivity of porous glasses saturated with sulfuric acid solutions was studied. At impregnating solution concentrations in the range 20–40 wt %, the glasses have high conductivities a σ > 0.1 ω^?1 cm^?1. The dependences of the electrical conductivity on parameters of the porous structure of membranes are considered.     

Temperature-concentration dependence of the electrical conductivity of glasses in the Zn(PO3)2-NaF system

Temperature-concentration dependence of the electrical conductivity in glasses of the Zn(PO₃)₂-NaF system was studied and compared with similar dependences for glasses of other systems. The extremal dependences log σ = f([Na⁺]) and {ie937-1} are interpreted from the standpoint of a macroscopically inhomogeneous structure of the glasses under study.     

Temperature dependence of photo-charge generation of polymeric photorefractive composite in the glass transition temperature region

For photo-charge generation of polymeric photorefractive (PR) composites, temperature is important factor with electric field, but no study for temperature dependence of photo-charge generation efficiency (φ) at the glass transition temperature (T_g) region has been done yet. In this work, we investigate the temperature dependency of φ of a low T_g PR composite. With increasing temperature the photo-charge generation efficiencies increased below T_g but decreased above T_g. This behavior could be attributed to temperature dependence of heat capacity and the dielectric constant of PR composite. The space charge field was strongly dependent on temperature and increased with increasing φ.     

Special features of the state of copper(II) oxide and its electric conductivity in porous glass

Controllable accumulation of copper(II) oxide in porous glass was carried out by repeated impregnation of the carrier by Cu(NO₃)₂ aqueous solutions with subsequent thermal decomposition of the salt. The results of measuring electric conductivity of a series of modified plates in combination with the data on the optical and X-ray electron spectroscopy make it possible to characterize two trends in the oxide distribution on a silica surface. In the case of its cyclic accumulation by small portions, a two-dimensional structure of monolayer filling the surface is presumably formed in a narrow range of CuO concentration, whereas the increase in the ??step?? of the accumulation gives rise to the formation and growth of island oxide particles.     

Temperature dependence of positron lifetime in ordered porous silica (SBA-3)

The temperature dependence of positron lifetime in uniform mesopores was analyzed. We used SBA-3 as the sample material, which possesses an ordered porous structure with uniform cylindrical mesopores. The positron lifetime corresponding to the annihilation in the mesopores increased gradually with a decrease in temperature down to 100 K, and its relative intensity also increased concomitantly. This result was attributed to the lower probability of the escape of the ortho-positronium (o-Ps) from the mesopores into the intergrain space at lower temperatures. An anomalous and sudden increase in the lifetime was observed at around 100 K; this result was in agreement with an increase in the positron lifetime reported in a previous study. It was revealed that the increase in the lifetime is very steep in cases of uniform mesopores, suggesting that the temperature dependence is influenced by the pore size.     

Temperature dependent electrical conductivity of polyaniline/Y2O3 composites

Composites of polyaniline with yttrium oxide (Y₂O₃) nanoparticles have been prepared by chemical polymerizations method by increasing the weight percentage of yttrium oxide. X-Ray diffraction (XRD) and Fourier Transform Infrared Spectra (FTIR) were used to characterize the composites. XRD and FTIR pattern indicate that Polyaniline (PANI) is intercalated into the layers of Y₂O₃ nanoparticles successfully by in situ polymerization and therefore the degree of crystallinity increases due to crystalline of yttrium oxide nanoparticles. The scanning electron micrographs (SEM) also confirm the formation of dual phase of platelet as well as of flaky structure in PANI-Y₂O₃. Temperature dependant DC conductivity showed three dimensional variable ranges hopping (3D VRH) model. Activation energy, density of states and hopping length are calculated and found to be influenced by intercalating PANI into the layers of Y₂O₃ clay.