烷基聚葡糖苷C9.6G1.3/n-C4H9OH/n-C6H14/H2O微乳液体系的介电弛豫谱研究

The pseudotertiary phase diagram of the microemulsion system alkyl polyglucoside/n-butanol/n-hexane/water was plotted at （30.0±0.1） ℃. The dielectric measurements, including permittivity, conductivity, relaxation strength, characteristic relaxation time, etc,, were applied to investigate the microstructure of the system. Unique dielectric relaxations were observed over the frequency range of 5-10^7 Hz, taking place possibly through an interracial polarization mechanism. According to the results obtained from dielectric spectroscopy, the structures of the microemulsion O/W, BC and W/O were determined, and some dielectric and phase parameters were calculated.     

Dilectric and thermal properties of PEO doped with cadimium chloride salt

The main aim of this research is to investigate the effect of salt concentration on the dielectric properties(AC (σ_AC),permittivity（ε′）,dielectric loss（ε″）,and dielectric relaxation process) and melting behavior of polyethylene oxide （PEO）/CdCl₂ complexes.The dielectric study was carried out over a frequency range 10-335 kHz and a temperature range 25-45℃.The AC conductivity,permittivity and dielectric loss of the PEO/CdCl₂ complexes increase with increasing salt concentration and temperature.Also,it was found that the addition of CdCl₂ salt to PEO host reduced the melting temperature of PEO host.Dielectric results reveal that the relaxation process of these complexes is due to viscoelastic relaxation or non-Debye relaxation at room temperature.Additionally,it was found that relaxation behavior remained viscoelastic at different temperatures and salt concentrations.     

DIELECTRIC PROPERTIES OF 1, 2-POLYBUTADIENES

The dielectric permittivity and loss tangent of 1,2-polybutadienes with different chain structures were determined as a function of temperature from-180℃ to 100℃ at different frequencies, and the frequency and structure dependence of the dielectric propertie of 1,2-polybutadienes have been investigated. It is found that a maximum of the permittivity occurs in the glass-transition region. The width of the glasstransition peak increases with increasing frequency while its height has little change. With a rise in the content of 1,2-units, the permittivity decreases and the height of the glass-transition peak slightly grows. A maximum of the width of the glass-transition peak appears when the content of 1,2-units is about 45%. Both the permittivity and dielectric loss drop down as the growth of the content of syndiotactic 1,2-units.     

Dielectric analysis on phase transition and micelle shape of polyoxyethylene trisiloxane surfactant in dilute aqueous solution

The cloudy Silwet L-77 aqueous solution on the concentration range from 0.5%to 50%was investigated by dielectric relaxation spectroscopy.The concentration dependence of phase microstructure was confirmed by means of analyzing the dielectric parameters of bulk solution.The relaxation behavior was assigned to the interfacial polarization between the micelle and the medium,and the relaxation distribution parameter was used to figure the shape transition from sphere to ellipsoid with the concentration increasing.The synchronous reduction of permittivity and conductivity indicated the formation of the lamellar phase. As compensation,the quantity of the surfactant liquid phase gradually decreased,whose shape constantly kept ellipsoidal.     

时域反射光谱法研究酰胺-醇混合物的介电驰豫

Using time domain reflectometry （TDR）, dielectric relaxation studies were carded out on binary mixtures of amides （N-methylformamide （NMF） and N,N-dimethylformamide （DMF）） with alcohols （1-butanol, 1-pentanol, 1- hexanol, 1-heptanol, 1-octanol, and 1-decanol） for various concentrations over the frequency range from 10 MHz to 10 GHz at 303 K. The Kirkwood correlation factor and excess dielectric constant properties were determined and discussed to yield information on the molecular interactions of the systems. The relaxation time varied with the chain length of alcohols and substituted amides were noticed. The Bruggeman plot shows a deviation from linearity. This deviation was attributed to some sort of molecular interaction which may take place between the alcohols and substituted amides. The excess static permittivity and excess inverse relaxation time values varied from negative to positive for all the systems indicating that the solute-solvent interaction existed between alcohols and substituted amides for all the dynamics of the mixture.     

时域反射光谱法研究酰胺-醇混合物的介电驰豫

Using time domain reflectometry (TDR),dielectric relaxation studies were carried out on binary mixtures of amides (N-methylformamide (NMF) and N,N-dimethylformamide (DMF)) with alcohols (1-butanol,1-pentanol,1-hexanol,1-heptanol,1-octanol,and 1-decanol) for various concentrations over the frequency range from 10 MHz to 10 GHz at 303 K. The Kirkwood correlation factor and excess dielectric constant properties were determined and discussed to yield information on the molecular interactions of the systems. The relaxation time varied with the chain length of alcohols and substituted amides were noticed. The Bruggeman plot shows a deviation from linearity. This deviation was attributed to some sort of molecular interaction which may take place between the alcohols and substituted amides. The excess static permittivity and excess inverse relaxation time values varied from negative to positive for all the systems indicating that the solute-solvent interaction existed between alcohols and substituted amides for all the dynamics of the mixture.     

Dielectric relaxation behavior of SDS/β-CD organized self-assembly in dilute aqueous solution

Dielectric relaxation behavior of SDS/β-CD self-organized with mass concentrations from 1% to 7% was investigated. The phase microstructure of SDS/β-CD aqueous solution was confirmed by analyzing the dielectric parameters. The dielectric relaxation behavior was attributed to the interfacial polarization between vesicle and medium, and the relaxation distribution parameter can indicate the shape transition from vesicles to microtubules with increasing concentration. Dielectric relaxation provided a new method to study surfactant organized self-assembly.     

FREQUENCY DEPENDENCE OF THE DIELECTRIC RELAXATION OF 1,2-POLYBUTADIENES

The dielectric loss factor and permittivity of a series of 1, 2-polybutadienes with different contents of 1, 2-units and different contents of syndiotactie 1, 2-units were determined over a frequency range from 30Hz to 100KHz at different temperatures. The WLF equation was evaluated for various samples with T_θat 100KHz as a reference temperature and the master curves of various samples have been constructed, which are in accordance with those calculated by Havriliak-Negami equation. The frequency dependence of the dielectric relaxation of 1, 2-polybutadienes was investigated over a frequency range from 10~0 Hz to 10~(12) ZHz in terms of the experimental data and the master curves.     

Phases confirmation of cloudy Silwet L-77 aqueous solution by dielectric relaxation spectroscopy

<正>The phase transition of Silwet L-77(a kind of siloxane surfactant) dilute aqueous solution with temperature was investigated by dielectric relaxation spectroscopy.In the initial heating process,a dielectric relaxation was found at about 10~6 Hz,which was considered as the interface polarization ascribed to the interface between water and liquid phases(W and L_1).With the temperature increasing further,a new dielectric relaxation was observed at about 10~4 Hz,which was assigned to the appearance of liquid crystal phase(L_α).According to the dielectric parameters fitted by Cole-Cole equation,the coexistence temperature of W,L_1 and L_αwas determined at about 37.0℃.     

Hydrolysis of Cephanone in SDS／n－C5H11OH／H2O System

The hydrolysis of cephanone in SDS micelle and SDS/n-C5H11-OH/H2O O/W microemulsion was studied through Uv-vis ab-sorption spectroscopy. The change of pH value in the hydrolysis of cephanone was determined. The result shows that pH value decreases in the process of the hydrolysis, and that the SDS ml-celle and SDS/n-C5H11OH/H2O O/W microemulsion accelerate the hydrolysis of cephanone compared with water.     

甲基丙烯酸甲酯、甲基丙烯酸乙酯与酚络合的介电驰豫行为

Dielectric absorption studies of H-bonded complexes of methyl methacrylate (MMA) and ethyl methacrylate (EMA) with p-cresol, p-chlorophenol, 2,4-dichlorophenol, and p-bromophenol were studied at microwave frequency 9.37 GHz in dilute solution of carbon tetrachloride at 308 K. Different dielectric parameters like dielectric constant ε' and dielectric loss ε' at microwave frequency, static dielectric constant ε0 and dielectric constant ε∞ at optical frequency were determined. The validity of the single frequency equation of Higasi et al. for multiple relaxation time τ(1) was found to be a function of the hydrogen bonding strength of phenolic hydrogen, whereas the group rotation relaxation time τ(2) was a function of the steric interaction of proton donor. The relaxation time was the maximumat 50:50 (molar ratio) of methacrylates with phenols.     

Dielectric Relaxation of Methyl Methacrylate and Ethyl Methacrylate on Complexation with Phenols

Dielectric absorption studies of H-bonded complexes of methyl methacrylate (MMA) and ethyl methacrylate (EMA) with p-cresol, p-chlorophenol, 2,4-dichlorophenol, and p-bromophenol were studied at microwave frequency 9.37 GHz in dilute solution of carbon tetrachloride at 308 K. Different dielectric parameters like dielectric constantε′ and dielectric loss ε″ at microwave frequency, static dielectric constant ε_0 and dielectric constant ε_∞ at optical frequency were determined. The validity of the single frequency equation of Higasi et al. for multiple relaxation time τ_(1) was found to be a function of the hydrogen bonding strength of phenolic hydrogen, whereas the group rotation relaxation time τ_(2) was a function of the steric interaction of proton donor. The relaxation time was the maximum at 50∶50 (molar ratio) of methacrylates with phenols.     

Electrochemical Oxidation of L-Cystenine in SDS／BA／H2O Microemulsion

The electrochemical oxidation of L-cysteine in an SDS/BA/H2O microemulsion system was studied with the methods of ultramicroelectrode cyclic voltammetry and AC impedance. The catalytic efficiency of the microemulsion on the electrochemical oxidation increases with the increase of BA or SDS content, but decreases with the increase of the water content because of the effects of BA, SDS and water on the solubilization of Lcysteine in the microemulsion. Furthermore, the catalytic efficiency of the bicontinuous structure is greater than that of an O/W microemulsion system. The results derived from both the rate constant k^0 and Gibbs free energy △G^≠ accord with those from the catalytic efficiency.     

Synergetic effects of silane-grafting and EVA on water tree resistance of LDPE

<正>The synergetic influence of silane-grafting and polar additives(EVA) on the water tree resistance of the low density polyethylene has been investigated.A series of samples obtained before and after hydration have been characterized by measuring gel content,infrared spectroscopy(FTIR),differential scanning calorimetry(DSC) and dielectric measurements.The results obtained clearly show that the silane condensation occurred and that the silane-grafting and polar additives have synergetic effects on the water tree resistance of LDPE with little influence on its dielectric properties,e.g.the dielectric breakdown strength,dielectric permittivity and loss tangent.     

Continuum Model for Electronic Polarization Based on a Novel Dielectric Response Function

A generalized response function based on the use of dielectric spectra for dielectric relaxation process is derived. We apply the general response function to the special case in order to examine how special dielectric relaxation functions developed by other authors for solvent relaxation can be derived based on our formulations. Three typical solvents, water, methanol, and acetonitrile are used to investigate the electronic polarization processes of polar solvents. The solvent electronic polarization process is shown after a linear variation with the external electric field imposed on the solvent. The results show a conclusion that the electronic polarization of the solvents will accompany the electronic transition synchronously, without time lag.     

时域反射谱法研究烷基丙烯酸酯与酚复合的介电弛豫

The dielectric relaxation measurements on binary mixtures of esters (methyl acrylate, ethyl acrylate, and butyl acrylate) with phenol derivatives (p-cresol, p-chlorophenol, and 2,4-dichlorophenol) were carried out at different concentrations at 303 K using the time domain reflectometry (TDR) over the frequency range from 10 MHz to 20 GHz. The Kirkwood correlation factor and excess inverse relaxation time were determined and discussed to yield information on the molecular interactions of the systems. The relaxation time increased with increasing concentration of phenols and increasing chain length of esters. The excess inverse relaxation time values were negative for all the systems, which indicated the solute-solvent interaction existing between esters and phenols producing a field in such a way that the effective dipole rotation was hindered.     

DIPOLE POLARIZATION RELAXATION AND MOLECULAR STRUCTURE OF MAIN-AND SIDE-CHAIN LIQUID-CRYSTALLINE POLYMERS

Molecular mobility in thermotropic polyesters and side-chain polymers with different struc-ture of mesogens and spacers has been studied by dielectrical method in dilutesolutions. The results made it possible to establish the multiplicity of dielectric relaxationtransitions which reflects the small- and large-scale types of molecular motion. It was shownthat dielectric relaxation processes occurring in accordance with local mechanism (relaxationtimes 10~(-9)--10~(-7)s. and the activation energy 10--50kJ/mol) are due to the mobility of kineticchain elements of different length within a monomer units. It was found that the dielectricrelaxation process connected with a large-scale form of molecular motion (relaxation times10~(-5)--10~(-6)s. and the activation energy 100kJ/mol) did not depend on the molecular massbut was infiuenced by factors changing the conformational state of the macromolecule. It isestablished tha the cooperative reorientation mobility of associated mesogenic fragments isthe source of the large-scale process.     

STUDY OF MICROWAVE REMOTE SENSING OF THE SOIL MOISTURE

This article includes a study of the microwave emissivity characteristics of moist soil and the method of microwave remote sensing of the soil moisture. The relation between soil dielectric constant and moisture was measured with terminal short circuit line method. The microwave emissivity of soil decreases with the increase of humidity because the real andimage parts of dielectric constant increases with the humidity. The relation between soil microwave emissivity and humidity is measured with the microwave emissivity meter made by us. Considerable change of brightness temperature is caused by different soil humidity. This article also presents the exhausted depth and the influence of humidity distribution on emissivity, the effection of soil surface roughness on emissivity. The theoretical analysis and experiment results have shown that microwave radiometer is a helpful instrument in the remote sensing of soil moisture. 3.2 cm waveband, with higher sensibility, deeper penetrate depth and less effect o     

RELAXATION IN DOMAINS:STRUCTURE AND SEGMENTAL DYNAMICS OF LC/I DIBLOCK COPOLYMERS

A series of block copolymers consisting of an isotropic (polystyrene) block and a side-chain liquid crystallineblock (LC) have been studied using small-angle X-ray scattering and dielectric spectroscopy. The triblock copolymer (PS-LC-PS) displays an order-to-order transition (OOT) together with the isotropic/nematic transition of the LC phase. The seriesof diblock copolymers show no clear OOT but the phase diagram differs from that of non-LC block copolymers. Thesegmental dynamics as measured with dielectric spectroscopy is dominated by the α and δ relaxation of the LC block. Bothdisplay a WLF like temperature dependence. The relaxation times are influenced by the constraints of the nanoscale domains.They are decreased for the LC confined in the domain as compared to the LC in the continuous matrix.     

Fabrication and characterization of gold nano particles for DNA biosensor applications

This research involves the preparation of a biosensor using silicon oxide for biomedical applications, and its effective use for the detection of target DNA hybridization. An electrochemical DNA biosensor was successfully fabricated by using(3-aminopropyl) tri-ethoxysilane(APTES) as a linker molecule combined with gold nanoparticles(GNPs) on a thermally oxidized SiO_2 thin film. The size of the GNPs was calculated by utilizing UV–vis data with an average calculated particle size within the range of 30±5 nm, and characterization by transmission electron microscopy(TEM) and atomic force microscopy(AFM). The GNP-modified SiO_2 thin films were electrically characterized through the measurement of capacitance, permittivity and conductivity using a low-cost dielectric analyzer. The capacitance, permittivity and conductivity profiles of the fabricated sensor clearly differentiated DNA immobilization and hybridization.