Electro-optic and dielectric behavior of a FLC material having doped with a non-mesogenic polar molecules

Liquid crystal mixtures of non-mesogenic polar molecule with a commercial ferroelectric liquid crystal (FLC) mixture were prepared. Two mixtures were prepared by mixing 0.5% (w/w) and 1% (w/w) of polar molecules with commercial FLC mixture. Comprehensive studies of dielectric and electro-optic properties of the commercial FLC mixture and the polar molecules doped FLC mixtures have been made as a function of temperatures. Our studies reveal a higher tilt angle in lower concentration (0.5%) mixture but in case of 1% mixture tilt angle is decreased in comparison to 0.5% mixture. The spontaneous polarization of the commercial FLC mixture and other two mixtures is almost equal in magnitude at all temperatures. At the lower temperature region of SmC¹ phase, Goldstone mode (GM) dielectric strength of the commercial FLC mixture and low concentration (0.5%) mixture is found almost equal but it is slightly higher in case of high concentration (1%) mixture. With the increase of temperature GM dielectric strength of both the doped mixtures rapidly converges at different temperatures which are much lower than the temperature of transition (T_C) from SmC¹ – SmA phase. The results have been discussed.     

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.     

Microwave dielectric absorption studies of hydrogen bonded polar binary mixtures of isobutanol with tertiary butyl amine

The dielectric behaviour of polar liquids like isobutanol, tertiary butyl amine and their equimolar binary mixture in nonpolar solvent benzene is studied in the microwave frequency range using the cavity perturbation technique at 6.218?GHz (J band), 9.880?GHz (X band), 16.331?GHz (P band) and 24.951?GHz (K band). Hamiltonian quantum mechanical calculations such as AM1, PM3 and MNDO optimized converged geometry operation is performed on isobutanol, tertiary butyl amine and their equimolar binary mixtures using Argus lab chemical modelling software, 2004. Dipole moments of the binary mixtures are calculated from the dielectric data using Higasi's method, and compared with the theoretical Hamiltonian quantum mechanical results. Conformational analysis of the formation of hydrogen bond between the isobutanol and tertiary butyl amine is supported by FT-IR and proton NMR spectra. The average relaxation times are calculated from their respective Cole–Cole plots.     

Dielectric properties of paper as a function of of moisture content at 9 GHz

This letter gives values of the complex dielectric constant of a good quality paper as a function of the moisture content at 9 GHz. The experimental results are interpreted using Weiner's theory for dielectric mixtures.     

Conformational and dielectric analysis of hydrogen bonded polar binary mixtures of propan-1-ol with propionaldehyde

The dielectric behaviour of polar liquids such as propan-1-ol, propionaldehyde and their equimolar binary mixture in non-polar solvent benzene is studied in the microwave frequency range using the cavity perturbation technique at 6.218 GHz (J band), 9.880 GHz (X band), 16.331 GHz (P band) and 24.951 GHz (K band). Ab initio geometry optimization is performed in the 6-31G (d) basis set using the Gaussian 94W program for both pure and binary systems of propan-1-ol and propionaldehyde. Dipole moments of the binary mixtures are calculated from the dielectric data using Higasi's method and compared with the ab initio results. Conformational analysis of the formation of hydrogen bond between the propan-1-ol and propionaldehyde is supported by the FT-IR spectra. The average relaxation times are calculated from their respective Cole–Cole plots.     

On the Viscoelastic and Dielectric Behavior of Some Organic Compounds and Their Binary Mixtures

The dependence of dielectric relaxation time on the viscosity of the medium is being extensively used to draw certain quantitative conclusions regarding molecular motion and inter-molecular forces in liquids, liquid mixtures, dilute solutions, and multi-component polar solutes in dilute solution. In the absence of proper empirical or theoretical equations for the variation of dielectric relaxation time with viscosity, only the experimental investigations on different systems can give an insight. In the present study, the results of dielectric measurements carried out on pure samples of bromohexane, bromooctane and bromodecane in dilute solutions in different mixed solvents (benzene + paraffin) and on binary mixtures (1 : 1) of (bromohexane + bromodecane); (bromodecane + propyl alcohol) and (propyl alcohol + methyl alcohol) are reported. For comparison, the results of bromodecane + propyl alcohol and propyl alcohol + methyl alcohol are chosen as they form examples of mixture of non-associative + associative and associative + associative liquids, respectively. Different parameters determined using these dielectric measurements are also presented using different models. These studies indicate that the dielectric behavior at microwave frequencies favor the concept of dynamic viscosity and a single viscoelastic relaxation time for the systems under study.     

Dielectric relaxation and hydrogen bond interaction study of diol-water mixtures

Complex dielectric permittivity measurements in the frequency range 10MHz-20GHz have been carried out in diol-water mixtures over the entire concentration range using a time domain reflectometry (TDR) method at 25°C. A hydrogen bonded theory is applied to compute the dielectric constant for the mixtures. It adequately reproduces the experimental values of static dielectric constants for the diol-water mixtures. The dielectric parameters confirm that the intermolecular homogeneous and heterogeneous hydrogen bonding vary significantly with the increase in concentration of the constituents of the diol-water mixtures.     

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.     

Understanding the molecular interaction and relaxation findings in amphiphilics on solution state using TDR

The dielectric behavior of stearic acid in 1,4-dioxane medium at various temperature 303 K–288 K and frequency regime (10 MHz–30 GHz) determined from the complex dielectric permittivity spectra obtained by Time Domain Reflectometry(TDR). In this frequency range, the dielectric study gives the electrostatic interaction as well as orientational polarizability of complex mixtures of long chain molecules significantly. Dielectric parameters were calculated from the complex spectra of the binary mixture by non linear least square fit method. The excess permittivity (ε^E), correlation factors were calculated for the binary system. Thermal parameters(ΔH-enthalpy, ΔS-entropy and ΔG-Gibbs free energy) were calculated and the direction of reaction is determined. The FTIR spectrum of the binary system recorded and the assignments are discussed. The FTIR spectral assignments confirm the molecular interactions.     

Achieving a multi-band metamaterial perfect absorber via a hexagonal ring dielectric resonator

A multi-band absorber composed of high-permittivity hexagonal ring dielectric resonators and a metallic ground plate is designed in the microwave band.Near-unity absorptions around 9.785 GHz,11.525 GHz,and 12.37 GHz are observed for this metamaterial absorber.The dielectric hexagonal ring resonator is made of microwave ceramics with high permittivity and low loss.The mechanism for the near-unity absorption is investigated via the dielectric resonator theory.It is found that the absorption results from electric and magnetic resonances where enhanced electromagnetic fields are excited inside the dielectric resonator.In addition,the resonance modes of the hexagonal resonator are similar to those of standard rectangle resonators and can be used for analyzing hexagonal absorbers.Our work provides a new research method as well as a solid foundation for designing and analyzing dielectric metamaterial absorbers with complex shapes.     

Impact of High-Dielectric-Loss Materials on the Microwave Field in EPR Experiments

A dielectric material distorts the microwave field inside an EPR resonator, which results in distortion of the EPR signal from spins inside the material. In this paper, the effects of a spherical bulb filled with a dielectric liquid such as water or a water–ethanol mixture were examined. EPR spectra were recorded for small samples inside and outside of the sphere. The studies include CW and ESE experiments at two microwave frequencies, X band (9.2 GHz) and L band (1.03 GHz). The double integral (area) of an EPR signal depends on[formula]at the position of the sample, causing a large difference in EPR signal intensities between samples in regions of different dielectrics. The phase of the EPR signal also is affected by the presence of the dielectric. These results were compared with three methods of calculating electromagnetic fields (quasi-static method, plane-wave-superposition method, and numerical analysis). Good agreement was found between experimental and calculated results.     

Structural study of aqueous solutions of tetrahydrofuran and acetone mixtures using dielectric relaxation technique

The complex permittivity, static dielectric constant and relaxation time for tetrahydrofuran-water and acetone-water mixtures have been determined at 0°, 10°, 25° and 35°C using time domain reflectometry technique (TDR). The behaviour of relaxation time of the mixture shows a maxima for the mixture with 30% of water by volume. This suggests that the tendency to form cluster between water and solute molecule is maximum for this mixture. The excess permittivity for both tetrahydrofuran-water mixture and acetone-water mixtures, are found to be negative. The Kirkwood correlation factor has been determined at various concentrations of water. Static dielectric constant for the mixtures have been fitted well with the modified Bruggeman model. The values of the Bruggeman parametera for tetrahydrofuran is found to be more than the corresponding value for acetone.     

Molecular associations in binary mixtures of pyridine and chlorobenzene in benzene solution using microwave absorption data

The dielectric relaxation time (τ) of binary mixtures of different molar concentrations of pyridine (C₅H₅N) and chlorobenzene (C₆H₅Cl) in benzene solution at different temperatures (25, 30, 35 and 40 °C) has been calculated by using standard microwave techniques and Gopala Krishna's single frequency (9.875 GHz) concentration variation method. The energy parameters (ΔH_ε, ΔF_ε, and ΔS_ε) for the dielectric relaxation process of the binary mixture containing 0.5 mol fraction of pyridine have been calculated at the respective temperatures. Comparisons have been made with the corresponding energy parameters for the viscous flow (ΔH_η, ΔF_η, and ΔS_η). From the observations it is found that the dielectric relaxation process can be treated as the rate process. Based upon above studies, solute–solvent type of molecular associations arising from the interaction of chlorobenzene and benzene and pyridine and benzene molecules has been proposed. No solute–solute type of molecular association has been observed.     

Dielectric absorption in mixtures of anisole with some primary alcohols at microwave frequency

Dielectric properties of binary mixtures of anisole with methanol (MeOH), 1-propanol (1-PrOH), 1-butanol (1-BuOH) and 1-heptanol (1-HeOH) over an entire concentration range have been studied at a fixed temperature 40°C. The dielectric constant (ε′) and dielectric loss (ε″) of the binary mixtures of polar liquids have been determined at a microwave frequency of 9.1?GHz. The static dielectric permittivity (ε ₀) of the liquid samples was also determined using a precision LCR meter. Determined values of static dielectric permittivity (ε ₀) and dielectric permittivity (ε*) at 9.1?GHz frequency were used to evaluate relaxation time (τ) and high frequency limit dielectric permittivity (ε _∞). Dielectric parameters were interpreted in terms of molecular interaction between the anisole and alcohol molecules.     

Microwave measurements and modelling of the permittivity of tropical vegetation samples

Microwave measurements of tropical vegetation samples (grass, casuarina, rubber leaf, rubber wood) at 9.5 GHz as a function of moisture content at 21°C are presented. A comparison is made with results calculated from six models for the permittivity of dielectric mixtures. Of these, only one of the models due to Polder, van Santen, and deLoor is found to give reasonable agreement, particularly for the real part of the permittivity. It is clear that more complex formulations for the permittivity of vegetation are necessary to model its behaviour as a function of moisture content and frequency.     

Dielectric relaxation study of ascorbic acid solutions in pure dimethylsulfoxide (or diethylsulfoxide) and in dimethylsulfoxide (or diethylsulfoxide)/water mixtures

The complex dielectric spectra of ascorbic acid solutions in pure dimethylsulfoxide (or diethylsulfoxide) and in dimethylsulfoxide (or diethylsulfoxide)/water mixtures have been measured at frequencies between 100 MHz and 20 GHz at 298.15 K.Two kinds of dielectric relaxation processes were observed in each solution. The low frequency relaxation (Debye term) is assigned to solute. The high frequency relaxation (Cole-Davidson term) is ascribed to practically unaffected solvent.From the results obtained it follows that relaxation time and relaxation strength in DESO containing solutions (i.e. binary AA/DESO and ternary AA/DESO/water systems) are greater than those in DMSO containing solutions.     

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.     

The attenuation of ultrasound in water-alcohol mixtures by the method of streaming

Experimental results on the attenuation of ultrasound in polar-polar liquid, that is, water-alcohol mixtures, by the method of streaming are presented. A comparative study of the results obtained by this method and those obtained by other methods has been made. Results of the present investigations agree well with those obtained by other workers. From the observed attenuation data, the bulk viscosity coefficients ‘b’ of the mixtures have been determined using Eckart's formalism on streaming.Satisfactory results could be obtained in the cases of water/methyl alcohol, and water/ethyl alcohol mixtures at all percentage compositions of mixtures but in the case of water/n-propyl alcohol satisfactory results could not be obtained at 5% to 40% mixture compositions. This observation bears the similarity with the cases of pure non-polar liquids. Here the observed results have been attempted to be explained, at least on the basis of relevant physical principles, in terms of dipole moment and dielectric constant.     

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.