Humidity Effect on Toluene Decomposition in a Wire-plate Dielectric Barrier Discharge Reactor

Laboratory-scale experiments were performed to evaluate the humidity effect on toluene decomposition by using a wire-plate dielectric barrier discharge (DBD) reactor at room temperature and atmospheric pressure. The toluene decomposition efficiency as well as the carbon dioxide selectivity with/without water in a gas stream of N₂ with 5% O₂ was investigated. Under the optimal humidity of 0.2% the characteristics of toluene decomposition in various background gas, including air, N₂ with 500 ppm O₂, and N₂ with 5% O₂ were observed. In addition, the influence of a catalyst on the decomposition was studied at selected humidities. It was found that the optimum toluene removal efficiency was achieved by the gas stream containing 0.2% H₂O, since the presence of water enhanced the CO₂ selectivity. In addition, the toluene removal efficiency increased significantly in a dry gas stream but decreased with an increase in the humidity when the Co₃O₄/Al₂O₃/nickel foam catalyst was introduced into the discharge area.     

Automatic measurement of the complex permittivity at millimeter wavelengths

A measuring system including an oversized cavity resonator operating in the TE₀₁ mode for the determination of the complex permittivity - j of low-loss liquids at frequencies of about 36 GHz is described. While is obtained by wavelength measurements in the filled and the empty resonator, is determined from the variation of the Q factor of the filled resonator with the length of the dielectric sample. The Q factors of values of about 2·10⁴ to 10⁵ can be measured automatically by means of a desk calculator which controls the frequency and collects the digitized values of the detector output voltage. By means of the calculator, the Q factors of the resonator are determined by fitting analytical (Lorentzian) resonance curves to the measurement data. and the Q factor for zero sample length are calculated according to Göttmann's methods.     

On the origin of the splittings of the ν3(SO4) modes in the specular reflectance IR spectra of gypsum

The IR polarized spectra of gypsum CaSO₄·2H₂O were recorded at incidence angles of approximately 10 and 16 degrees. Band singlet or doublet was observed for the higher frequency ν₃(SO₄²⁻) mode of B_u symmetry type, depending on polarization (n or p). A doublet was observed for the lower frequency ν₃(SO₄²⁻) mode of B_u symmetry type too, irrespectively of the type of polarization. In order to give an explanation for the doublets origin, a model permittivity function was constructed. Quite good agreement exists between the reflectance based on the model permittivity function and the experimentally measured one for the high-frequency doublet. The origin of the lower frequency doublet could not be explained in this way, but may be speculated to result from an Evans type interaction between a combination of a water libration and ν₂(SO₄²⁻), with the lower frequency ν₃(SO₄²⁻) mode.     

26种材料能量损失函数的计算研究

计算拟合了26种块体材料的能量损失函数,包括18种单质材料（Ag、Al、Au、C、Co、Cs、Cu、Er、Fe、Ge、Mg、Mo、Nb、Ni、Pd、Pt、Si、Te）和8种化合物（AgCl、Al₂O₃、AlAs、CdS、SiO₂、ZnS、ZnSe、ZnTe）.基于Drude-Lindhard模型,将实验测得的能量损失函数拟合为有限个解析函数,通过求和规则验证了拟合结果的准确性.基于拟合结果,模拟了反射电子能量损失谱,模拟结果与实验结果一致.所有材料能量损失函数的拟合参数均在线公开,地址为http：//micro.ustc.edu.cn/ELF/ELF.html.     

Investigation of thermo-electro-optic properties of some mixed nematic liquid crystals

The 6CB/8CB/8OCB liquid crystal mixture has been studied by Differential Scanning Calorimetry (DSC), polarised optic microscopy (POM), Semiconductor Characterization System, and Ultra-violet spectrophotometry (UV). DSC and POM results indicate that the 6CB/8CB/8OCB mixture exhibits liquid crystalline properties. The capacitance-voltage and conductance-voltage measurements were performed in the frequency range of 200-500 kHz and in the temperature range of 30oC–50oC. The 6CB/8CB/8OCB mixture showed an extremely large positive dielectric anisotropy. The molar absorptivity ? for the 6CB/8CB/8OCB mixture was calculated and found to be higher than the absorptivity values of the binary mixtures due to the alkyl chain length with H-aggregation.     

Dielectric Relaxation Spectroscopy of Liquid Crystal in Nematogenic Mesophase

In the present study, we report the dielectric behavior of a high temperature nematic liquid crystal (NLC) in both the planar as well as homeotropic alignments. To understand the mechanism of such high temperature NLC, we have performed dielectric spectroscopy in frequency range 100 Hz to 10 MHz. The different dielectric parameters, viz., effective dielectric permittivity and dielectric anisotropy of the sample have been determined with the variation of frequency and temperature. It is found that the dielectric parameters depend on dipole moment and rotation of side chain of molecule. The phase transition of this high temperature NLC has been confirmed by the DSC study.     

Deposition and dielectric characterization of strontium and tantalum-based oxide and oxynitride perovskite thin films

We have synthesized the composition x = 0.01 of the (Sr_1-xLa_x)₂(Ta_1-xTi_x)₂O₇ solid solution, mixing the ferroelectric perovskite phases Sr₂Ta₂O₇ and La₂Ti₂O₇. Related oxide and oxynitride materials have been produced as thin films by magnetron radio frequency sputtering. Reactive sputter deposition was conducted at 750 °C under a 75 vol.% (Ar) + 25 vol.% (N₂,O₂) mixture. An oxygen-free plasma leads to the deposition of an oxynitride film (Sr_0.99La_0.01) (Ta_0.99Ti_0.01)O₂N, characterized by a band gap E_g = 2.30 eV and a preferential (001) epitaxial growth on (001) SrTiO₃ substrate. Its dielectric constant and loss tangent are respectively Epsilon' = 60 (at 1 kHz) and tanDelta = 62.5 × 10⁻³. In oxygen-rich conditions (vol.%N₂ ≤ 15%), (110) epitaxial (Sr_0.99La_0.01)₂(Ta_0.99Ti_0.01)₂O₇ oxides films are deposited, associated to a larger band gap value (E_g = 4.55 eV). The oxide films permittivity varies from 45 to 25 (at 1 kHz) in correlation with the decrease in crystalline orientation; measured losses are lower than 5.10⁻³. For 20 ≤ vol.% N₂ ≤ 24.55, the films are poorly crystallized, leading to very low permittivities (minimum Epsilon' = 3). A correlation between the dielectric losses and the presence of an oxynitride phase in the samples is highlighted.     

Strong light‐matter coupling between a molecular vibrational mode in a PMMA film and a low‐loss mid‐IR microcavity

Microcavity devices exhibiting strong light‐matter coupling in the mid‐infrared spectral range offer the potential to explore exciting open physical questions pertaining to energy transfer between heat and light and can lead to a new generation of efficient wavelength tunable mid‐infrared sources of coherent light based on polariton Bose‐Einstein Condensation. Vibrational transitions of organic molecules, which often have strong absorption peaks in the infrared and considerably narrower linewidths than organic excitonic resonances, can generate polaritonic states in the mid‐infrared spectral range using microcavity devices. Here, narrow linewidth polaritonic resonances are exhibited in the mid‐infrared by coupling the carbonyl stretch vibrational transition of a polymethyl methacrylate film to the photonic resonance of a low optical‐loss mid‐infrared microcavity, which consisted of two Ge/ZnS dielectric Bragg reflectors. Rabi‐splitting of 14.3 meV is observed, with a 4.4 meV polariton linewidth at anti‐crossing. The large Rabi‐splitting relative to linewidth indicates efficient impedance‐matching between the bare vibrational and photonic states, and suggests molecular‐vibration polaritons incorporated in dielectric microcavities can be an enabling step towards realizing polariton optical switching and polariton condensation in the mid‐infrared spectral range.     

The enhancement of the oxidation resistance of carbonyl iron by polyaniline coating and consequent changes in electromagnetic properties

In order to enhance the stability of commercially unmodified processed carbonyl iron (CI) and to prevent corrosion, CI powders were coated with polyaniline (PANI) by using surfactant-stabilized PANI colloids in chloroform. PANI coats the individual particles with a film of a few micrometres thickness. Electromagnetic properties, as well as thermal and storage stability, of polymer composites filled with pristine and PANI-coated CI have been studied. The PANI overlayer has negligible influence on the magnetic and dielectric spectra of CI-filled polymer composites at ambient temperature. However, the temperature-frequency study of complex permittivity demonstrated that the composites containing PANI-coated CI powders are characterized by temperature-independent dielectric spectra, whereas the complex permittivity of polymer composites with pristine powders drastically decreased at elevated temperature. Additionally, the thermogravimetric analysis of pristine and PANI-coated CI powders in air has shown improvement in the stability. PANI overlayer prevents the oxidation of particles and acts as corrosion protection of CI.