Dielectric relaxation studies of aqueous sucrose in ethanol mixtures using time domain reflectometry

Time domain reflectometry method has been used in the frequency range of 10 MHz to 10 GHz to determine dielectric properties of aqueous sucrose in ethanol. The dielectric parameters, i.e., static dielectric constant and relaxation time were obtained from the complex permittivity spectra using the non-linear least squares fit method. The Luzar theory is applied to compute the cross-correlation terms for the mixtures. It adequately reproduces the experimental values of static dielectric constants. The Bruggeman model for the non-linear case has been fitted to the dielectric data for mixtures.     

Study of activation parameters and NMR spin-lattice relaxation time in some substituted amines

The present communication reports the experimental values of NMR spin-lattice relaxation time (T₁) and dielectric relaxation time (τ) of piperidine, pyrrole, pyridine, diethylamine, triethylamine and pyrrolidine. The values of activation energy (ΔE_A) obtained using dielectric relaxation time, have been correlated with calculated values of ΔE_A obtained using Arrhenius equation of NMR relaxation time (T₁) for pyridine, diethylamine and pyrrole. Authors have also established a correlation between the experimental values of NMR spin-relaxation time (T₁) with its calculated values obtained using different equations of dielectric relaxation time (τ).     

Dielectric relaxation study of pyridine-alcohol mixtures using time domain reflectometry

Time domain reflectometry is applied to dielectric relaxation measurements on pyridine-alcohol (methanol, ethanol, propan- 1-o1 and butan-1 -o1) mixtures over the entire concentration range and over the frequency range 10MHz-10GHz at 5, 15, 25 and 35°C. From the data, static permittivity and the dielectric relaxation time are extracted using a bilinear calibration method and a nonlinear least-squares fit method. These mixtures exhibit a principal dispersion of the Debye type at microwave frequencies. The Kirkwood correlation factor, which contains information regarding solute-solvent interaction and corresponding structural information, was obtained for these systems, and the excess inverse relaxation time and molar energy of activation for all these systems were determined. The values of the static permittivity, the relaxation time and the Kirkwood correlation factor decrease with increased pyridine concentration in alcohol. The static permittivity of the mixtures fits the modified Brugemann model well.     

Study of heterogeneous interaction in binary mixtures of 2-methoxyethanol-water using dielectric relaxation spectroscopy

The dielectric relaxation measurements on binary mixtures of 2-methoxyethanol with water have been carried out over entire concentrations and at temperature range of 0 °C to 25 °C using a picosecond time domain reflectometry technique. The complex dielectric permittivity spectra of 2-methoxyethanol/water mixtures were fitted using Havriliak-Negami equation. The static dielectric constant and relaxation time for all concentrations were obtained using least square fit method. The principal relaxation time is small if compared to that of corresponding alcohol/water mixtures this may be due to the hydrogen bonding ether oxygen in the 2-ME-water system. Excess dielectric properties, Kirkwood correlation factor, thermodynamic properties and Bruggeman factor are also determined and the results are interpreted in terms of heterogeneous interactions among the unlike molecules due to hydrogen bonding.     

Dielectric behaviour of aqueous CsCl solutions

Complex dielectric permittivity spectra, in the frequency range 10 MHz to 20 GHz are reported for aqueous cesium chloride (CsCl) solutions at 250C using time domain reflectometry technique. The static dielectric constant, relaxation time and conductivity have been determined using nonlinear least squares fit method. From the static dielectric constant, hydration numbers were determined by using measured solutions density at different concentrations.     

Dielectric and thermodynamic properties of CHF3 near the critical temperature

We report here some measurements of the complex dielectric constant of CHF₃ near the critical temperature from the low pressure gas densities up to the compressed liquid ones. The behaviour of the complex dielectric constant, measured at about 10 GHz, is compared with the provisions of some recent theories. The dielectric relaxation time is derived and an interpretation of the relaxation mechanisms in the whole explored density range is proposed. The pressure second virial coefficient is also obtained.     

Parameters of LC molecules’ movement measured by dielectric spectroscopy in wide temperature range

Dielectric properties of a nematic liquid crystal (NLC) mixture ZhK-1282 were investigated in the frequency range of 10²–10⁶Hz and a temperature range of ?20 to 80?°С. On the basis of the Debye’s relaxation polarization model dielectric spectra of temperature dependence of the orientational relaxation time τ and the dielectric strength δe were numerically approximated at the parallel orientation of a molecular director relative to alternating electric field. Influence of ester components in the mixture plays crucial role in relaxation processes at low temperature and external field frequency. The activation energy of the relaxation process of a rotation of molecules around their short axis was measured in a temperature interval of ?20 to ?+15?°С in which the dispersion of a longitudinal component of the dielectric constant takes place. The energy of potential barrier for polar molecules rotation in the mesophase was calculated. The value of the transition entropy from the nematic to isotropic phase was obtained from this calculation. The values of the coefficient of molecular friction and rotational diffusion were obtained by different methods. The experimental data obtained are in a satisfactory agreement with the existing theoretical models.     

Mechanisms of dielectric polarization in thermotropic liquid-crystalline complexes based on lanthanides

The components of the dielectric constant of a terbium-based liquid-crystalline complex have been measured in the frequency range of 350–5 × 10⁶ Hz. The magnitude and sign of the dielectric anisotropy of the complex have been determined. Dispersion of the dielectric constants in the liquid-crystalline and isotropic phases has been found. The mechanisms responsible for the relaxation phenomena that appear in the studied sample have been determined. The time of dielectric relaxation, the activation energy, and the dipole moment of the complex have been obtained.     

Dielectric behaviour of propylene glycol-water mixtures studied by time domain reflectometry

Dielectric relaxation measurements on water mixtures of propylene glycol across the entire concentration range were carried out using time domain reflectometry at 25°C over the frequency range from 10 MHz to 4 GHz. For all the mixtures, only one dielectric loss peak was observed in this frequency range. The relaxation in these mixtures can be described by a single relaxation time using the Debye model. A plot of the calculated relaxation time of the mixtures gives a straight line against the mole fraction of water, X_w. It is reasoned that the diameter of the water cluster is nearly the same as the length of propylene glycol. Further, a plot of the dielectric relaxation strength δ? against X_w suggests that there is a changing pattern of dielectric behaviour from below X_w = 0.5 to higher values of X_w. The excess permittivity, the excess inverse relaxation time and the activation free energy have been determined, to confirm the formation of hydrogen bonded homogeneous and heterogeneous cooperative domains, the dynamics of solute-solvent interaction and the hindrance to molecular rotation in the hydrogen bonded glass forming propylene glycol-water system.     

Dielectric relaxation and related studies of 4-ethylphenol-methanol mixtures using time domain reflectometry

The dielectric relaxation studies of 4-ethylphenol-methanol mixtures have been carried out at various temperatures ranging from 10°C to 40°C using time domain reflectometry in the frequency range 10 MHz to 10 GHz. The relaxation mechanism in these systems is explained by Cole-Davidson model. The excess dielectric parameters, Kirkwood correlation factor and activation energy have been calculated and discussed with respect to molecular arrangements, and microdynamics of the binary mixture composed of both the associative type of liquids.     

Dielectric studies of alkyl acrylates with primary alcohols using time domain reflectometry

Binary polar–polar liquid mixtures of alkyl acrylates (methyl acrylate, ethyl acrylate and butyl acrylate) with primary alcohols (propan-1-ol, butan-1-ol and hexan-1-ol) were subjected to dielectric studies at 303?K for different concentrations using time domain reflectometry (TDR) over the frequency range from 10?MHz to 10?GHz. Static permittivity (ε₀) dielectric constant at high frequency (ε_∞) and relaxation time (τ) were found through dielectric measurements for different concentrations of each system. The Bruggeman dielectric factor, Kirkwood correlation factor and the excess inverse relaxation time were determined and discussed to yield information on the molecular interactions of the systems. Deviations from the linearity of various models suggest molecular association through hydrogen bonding between the ?OH group of alcohols and C=O group of esters. The results also show a dependence of dielectric parameters on the alkyl chain length of both the alcohols and esters.     

Dielectric relaxation studies of alkanols solubilized by sodium dodecyl sulphate aqueous solutions

Considerable attention has been paid in recent years to the influence of alcohols on ionic micellar structures, alcohol co-surfactants most commonly employed in the preparation of microemulsions. Dielectric relaxation spectroscopy (DRS) is a versatile tool to monitor the dynamic process of such micellar systems. We report here the changes in the dielectric constant of the medium and the relaxation time of micellar solutions of sodium dodecyl sulphate (SDS) in water in the presence and absence of alkanols—hexan-1-ol, octan-l-ol, decan-l-ol and 1,2-ethanediol. The time domain dielectric data were obtained in the reflection mode in the frequency range of 10 MHz to 20 GHz using a HP54750A sampling oscilloscope and HP 54754A TDR plug-in-module. The sample is held at 303 K in a SMA cell with an effective pin length of 1.35 mm. We have determined the relaxation time (τ) using the Cole–Cole method. The relative viscosity ηr on the micellar solutions were also determined. The result shows that the dielectric constant increases linearly with SDS concentration in pure aqueous solutions up to 400 mM and decreases thereafter. The relaxation times are of the order of 15 ps to 25 ps and are far greater than that of Debye rotational relaxation of the monomer species. It is assigned to the dispersion step to water molecules surrounding to hydrophobic particles or the “bound water”. The addition of alcohols results in a linear increase in relaxation time in all the systems. As the concentration of SDS increases τ/ηr attains a near constant value showing that solubilization becomes more difficult at these concentrations. Our results show that the alcohol molecules are solubilized at the surface of the SDS micelle (i.e.) the micelle–water interface.     

ZnO-Bi2O3系压敏陶瓷的晶界电子结构

测量了ZnO-Bi₂O₃系压敏陶瓷在不同温度下的介电频谱,基于压敏陶瓷介电特征损耗峰起源于耗尽层内本征缺陷电子松弛过程的理论,计算了ZnO的本征缺陷结构,并进一步求出了晶界的微观电参数和宏观单晶界击穿电压.单晶界击穿电压的理论值与实验测量值符合得很好,这表明本文建立的基于介电谱计算本征缺陷的方法是有效的. 关键词： ZnO压敏陶瓷 晶界电子结构 介电谱     

Electric Modulus Spectroscopic Studies of the Dielectric Properties of Carbon Nanotubes/Epoxy Polymer Composite Materials

The electrical properties of epoxy polymer/carbon nanotubes composites were characterized using impedance spectroscopy in the frequency range between 1 Hz and 10 MHz and temperature range between 25°C and 105°C. We report the analysis of the experimental data using the electric modulus formalisms to understand the dielectric relaxation mechanisms. The variation of the real and imaginary parts of the electric modulus versus frequency and temperature were suggestive of two relaxation processes, associated with dipolar relaxation and CNT-polymer interfaces. The Havriliak-Negami model of dielectric relaxation was used for modelling the relaxation processes, extracting the relaxation parameters.     

Dielectric relaxation spectrum of water studied by the site—site generalized Langevin/modified mode-coupling theory

The dielectric relaxation spectrum of water is calculated from the site-site generalized Langevin/modified mode-coupling theory. The main part of the relaxation follows the Debye-type function, and a small deviation from the Debye relaxation is found on the high-frequency side. This tendency is consistent with recent experiments, although the absolute relaxation time does not agree with the experimental value quantitatively. The time development of the longitudinal polarization function resembles the dielectric part of the memory function, and we consider that this is because the dielectric friction dominates the collective reorientation of the dipole moment of water. We performed calculations with different dielectric constants using the reference interaction-site model integral equation, and found that the large gap between the time scales of the dielectric relaxation and the longitudinal polarization relaxation causes the Debye-type dielectric relaxation in our theory when the dielectric friction is dominant in the friction on the collective reorientation of the dipole moment. Namely, the longitudinal polarization relaxation is fast enough to be considered as a white noise to the dielectric relaxation process, so that the relaxation becomes a Markov process. The large gap between the two relaxation times originates from a large local field correction owing to the large dielectric constant of water. It is also suggested that the deviation from the Debye relaxation at the high-frequency side is the manifestation of the slow memory caused by the long-time part of the longitudinal polarization relaxation in the low-wavenumber region.     

Non-markovian properties of dielectric relaxation in liquids

Statistical molecular memory is investigated in dielectric relaxation in a liquid medium. A new method of closing the infinite chain of kinetic equations for the time correlation function is proposed, and used to obtain an equation permitting the calculation of the smallest-order memory functions. The spectrum of the non-Markovian parameter obtained indicates that dielectric relaxation in liquid CH₃I is a significantly non-Markovian process.Kazan' State Pedagogical Institute. Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 10, pp. 27–31, October, 1995.     

自由和随机介电弛豫

本文介绍一种傅里叶变换介电谱仪方法,它可简化解谱过程,并节省数据内存量,使用这台仪器证明了同一电介质样品在不同条件下自由或随机弛豫可出现于10⁶至10^-4s的时间范围,这和唯象理论的预言一致,弛豫时间与连接样品两个电极的测量电路的电阻R有关,大的R值给出开路弛豫时间,小的R值导致短路极限,开路弛豫时间比短路值可以大10⁶倍,给出了从开路到短路情况复介电常数频域谱的变化。     

Shear Stress and Dielectric Analysis of H3PO4 Doped Polyaniline Based Electrorheological Fluid

We synthesized phosphoric acid (PA) doped polyaniline (PANI) particles (PANI‐PA) and investigated their electrorheological (ER) and dielectric characteristics when they were dispersed in silicone oil. Flow curves of the PANI‐PA based ER fluid under several applied electric field strengths were analyzed using a shear stress model. We also examined ER characteristics based on the relaxation time obtained from the dielectric spectrum.     

Glass transitions and dynamics in thin polymer films: dielectric relaxation of thin films of polystyrene

The glass transition temperature T(g) and the temperature T(alpha) corresponding to the peak in the dielectric loss due to the alpha process have been simultaneously determined as functions of film thickness d through dielectric measurements for polystyrene thin films supported on glass substrate. The dielectric loss peaks have also been investigated as functions of frequency for a given temperature. A decrease in T(g) was observed with decreasing film thickness, while T(alpha) was found to remain almost constant for d>d(c) and to decrease drastically with decreasing d for d相似文献   

Dielectrics with strong and weak processes of polarization relaxation

The relationships between electrical parameters of layers needed both for the transition from strong to weak relaxations and for when there are no extrema in the relation between frequency and the dielectric loss tangent and imaginary parts of dielectric permeability are determined using a model for a double-layered dielectric with the serial inclusion of strata. The literature data was analyzed, allowing us to discover heterogeneous materials with developing strong and weak relaxation polarization. Materials for which the mean time of relaxation for dielectric permeability and conductivity differ were found.