Kinetics of the reactions of C2H5, n‐C3H7, and n‐C4H9 radicals with Cl2 at the temperature range 190–360 K

The kinetics of the C₂H₅ + Cl₂, n‐C₃H₇ + Cl₂, and n‐C₄H₉ + Cl₂ reactions has been studied at temperatures between 190 and 360 K using laser photolysis/photoionization mass spectrometry. Decays of radical concentrations have been monitored in time‐resolved measurements to obtain reaction rate coefficients under pseudo‐first‐order conditions. The bimolecular rate coefficients of all three reactions are independent of the helium bath gas pressure within the experimental range (0.5–5 Torr) and are found to depend on the temperature as follows (ranges are given in parenthesis): k(C₂H₅ + Cl₂) = (1.45 ± 0.04) × 10^?11 (T/300 K)^{?1.73 ± 0.09} cm³ molecule^?1 s^?1 (190–359 K), k(n‐C₃H₇ + Cl₂) = (1.88 ± 0.06) × 10^?11 (T/300 K)^{?1.57 ± 0.14} cm³ molecule^?1 s^?1 (204–363 K), and k(n‐C₄H₉ + Cl₂) = (2.21 ± 0.07) × 10^?11 (T/300 K)^{?2.38 ± 0.14} cm³ molecule^?1 s^?1 (202–359 K), with the uncertainties given as one‐standard deviations. Estimated overall uncertainties in the measured bimolecular reaction rate coefficients are ±20%. Current results are generally in good agreement with previous experiments. However, one former measurement for the bimolecular rate coefficient of C₂H₅ + Cl₂ reaction, derived at 298 K using the very low pressure reactor method, is significantly lower than obtained in this work and in previous determinations. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 614–619, 2007     

Higher order symmetrizer and application to an unusual transport equation

We study a class of stationary transport equation with nonlocal low-order tems We obtain the existence and uniqueness of a solution in sobolev spaces     

Modifying gradient theory to predict the surface properties of halogenated hydrocarbons

A new method is proposed for predicting the surface tension, density profile, and thickness of the surface layer of a liquid near an interface using gradient theory. The objects of study are halogenated hydrocarbons. The algorithm for calculating surface properties includes a new modification of the Peng-Robinson cubic equation of state (EoS) that does not require information on the critical parameters, and a new procedure for calculating the influence parameter. Validation of the procedure for predicting the surface properties of liquids shows that the agreement between the calculated surface tension of halogenated hydrocarbons and the existing literature data is sufficient for practical use.     

求解复杂湍流的非线性涡黏性系数模型和代数应力模型

非线性涡黏性系数模型和代数应力模型联系了线性涡黏性系数湍流模型和完整的微分 雷诺应力模型.随着它们受到日益关注,其形式也越来越多样化.本篇综述的目的是对这些模 型加以总结并比较它们之间的共同点及不同之处,指出它们与完整微分雷诺应力模型之间的 关系,以及相对于线性涡黏性系数模型而言它们在预报流场上所具有的优势.     

Nonlinear absorption, linear optical properties and structure of CdSXSe1−X microcrystallites in glass matrix

It was found that optical properties and nonlinearity of semiconductor microcrystallites in glass matrix are determined mainly by their structure. We established that the Auger recombination and the traps filling are responsible for the intensity dependence of transmission at picosecond and nanosecond pump respectively. The probabilities of linear and Auger recombination as a function of intensity have been obtained by computer simulation.     

Polarization behaviour of paper during corona charging

The polarization phenomenon of papers containing different amounts and different types of inorganic fillers during corona charging was studied using a dose-charging method. This method enables to investigate the phenomena in the conditions close to the real ones. It revealed that the paper composition affects the polarization tendency during the corona charging of paper. The filler influences the paper's dielectric constant and hence its electrical capacitance, charging potential and polarizing electric field. It was shown that paper polarization depends mainly on the electric field and this is caused by the orientation polarization and the role of the filler origin and its concentration in the polarization was surprisingly low. Polarization temperature dependences enable to propose the paper polarization mechanism. Paper polarizability is dominated by cellulose and the moisture content in it, and the liability of cellulose and hydrogen bonds hydroxyl groups.     

Determination of electron affinity of carbonyl radicals by means of negative ion mass spectrometry

Appearance energies of [M-H](-) ions from carbonyl compounds R-CO-R' (R,R' = H, CH(3), NH(2), OH) have been measured by means of negative ion mass spectrometry in resonant electron capture mode. Values of electron affinity of the corresponding radicals, CH(2)&dbond;C(X)O, NH&dbond;C(X)O and O&dbond;C(X)O, have been determined. Copyright 1999 John Wiley & Sons, Ltd.     

Cavity ring-down spectroscopy of OH radicals in low pressure flame

10 molecules/cm³) and large dynamic range (more than 20 000) are demonstrated. CRDS also provides accurate temperature measurements, with statistical errors less than 2%. Measured concentration profiles are in reasonable agreement with calculated values. It is observed that in the preflame zone (where the temperature is about 1000 K), the OH concentration at the first vibrational excited state is about seven times larger than the equilibrium OH(v”=1) concentration at this temperature. Received: 24 June 1997/Revised version: 12 September 1997     

The multi-functional aspect of scanning holographic microscopy: a review(Invited Paper)

Recent developments in scanning holographic microscopy that offer the prospects of new quantitative tools and imaging modalities in bio, micro, and nano sciences are reviewed. The versatility of the method is emphasized. Scanning holography can operate in an incoherent mode for fluorescence imaging, in a coherent mode for quantitative phase imaging, or in a tomographic mode for axial sectioning and rejection of the out-of-focus haze. Possible applications are illustrated with examples, and future prospects ...