The Millimeter Wave Tomography Application for the Subsurface Imaging

In the present paper new results of modeling and experimental investigation on millimeter wave subsurface tomography are submitted. Tomographic algorithm is employed for imaging of subsurface objects in the case when conductivity of probed medium is not equal to zero. The possibilities and restrictions of this algorithm for image processing are shown both as a result of modeling and as a result of experiments. A new tomography setup allowing obtaining images of different inhomogeneities in dielectric media is considered.     

A periodic DFT study of water and ammonia adsorption on anatase TiO2 (001) slab

Water and ammonia adsorption mechanisms on anatase TiO₂ (001) slab surface are investigated by means of periodic DFT approach. Molecular and dissociative adsorption energies for water are calculated to be ? 15 kcal/mol and ? 32 kcal/mol, respectively. Similarly, molecular and dissociative adsorption energies of ammonia on the same surface are found as ? 25 kcal/mol and ? 20 kcal/mol. A reverse result in this order is reached for the previous case of ONIOM cluster study (? 23 kcal/mol and ? 37 kcal/mol, respectively). The vibration frequency values are computed for the optimized geometries of adsorbed water and ammonia molecules on anatase TiO₂ (001) slab surface and compared with the values reported in the literature.     

Precovering and Preenveloping Ideals

In [8 Salce , L. ( 1979 ). Cotorsion theories for abelian groups . Symposia Mathematica 23 : 11 – 23 . [Google Scholar]] L. Salce introduced the notion of a cotorsion pair (?, 𝒞) in the category of abelian groups. But his definitions and basic results carry over to more general abelian categories and have proven to be useful in a variety of settings. A significant result of cotorsion theory proven by Eklof and Trlifaj is that if a pair (?, 𝒞) of classes of R-modules is cogenerated by a set, then it is complete [1 Eklof , P. C. , Trlifaj , J. ( 2001 ). How to make Ext vanish . Bull. London Math. Soc. 33 : 31 – 41 .[Crossref], [Web of Science ®] , [Google Scholar]]. Recently Fu, Herzog, Guil, and Torrecillas developed the ideal approximation theory [6 Herzog , I. ( 2014 ). Phantom morphisms and Salce's Lemma . Contemp. Math. 607 : 57 – 83 .[Crossref] , [Google Scholar]], [4 Fu X. H. , Guil Asensio , P. A. , Herzog , I. , Torrecillas , B. ( 2013 ). Ideal Approximation Theory . Adv. in Math. 244 : 750 – 790 .[Crossref], [Web of Science ®] , [Google Scholar]]. In this article we look at a result motivated by the Eklof and Trlifaj argument for an ideal ? when it is generated by a set of homomorphisms.     

A monopole-like classical solution to a purely fermionic model of even dimensions

We present a static solution to the classical field equations of a purely spinorial model with SO(2n) internal symmetry in 2n dimensions. The model contains composite vector fields which have solutions of the Wu-Yang monopole type.     

Elemental Analysis of Tarhana by Microwave Induced Plasma Atomic Emission Spectrometry

Elemental analysis of tarhana, a traditional Turkish cereal soup, has been conducted. A new method was developed for the determination of calcium, iron, magnesium, manganese, potassium, and sodium, in tarhana by microwave induced plasma atomic emission spectrometry. A sample of 0.1?g were mineralized by microwave digestion in 10?mL of 65% HNO₃. A wheat flour standard reference material (GBW 08503) was used for validation. Linear calibration using standards prepared in acid was conducted for all determinations. The limits of detection were 1.21?µg?g^?1 for Ca at 393.366?nm, 0.43?µg?g^?1 for Fe at 259.940?nm, 11.5?µg?g^?1 for K at 766.491?nm, 0.12?µg?g^?1 for Mg at 285.213?nm, 0.04?µg?g^?1 for Mn at 403.076?nm, and 0.04?µg?g^?1 for Na at 588.995?nm. Ca, K, Fe, Mg, Mn, and Na were determined in tarhana with values from 0.73 to 1.61, 0.016 to 0.061, 2.02 to 4.09, 0.473 to 1.414, 0.019 to 0.043, and 0.26 to 1.83?mg?g^?1, respectively.     

Ethylene epoxidation catalyzed by chlorine-promoted silver oxide

It is demonstrated that, on a silver oxide surface, direct formation of ethylene oxide (EO) through the reaction between gas phase ethylene and surface oxygen is possible. The direct reaction channel produces EO selectively without competing with acetaldehyde (AA) formation. The oxometallacycle (OMC) forms on an oxygen vacant surface and reduces EO selectivity. Cl adsorption removes these surface vacant sites and hence prevents the formation of the OMC intermediate.     

Determination of Chlorine in Plastics via SrCl by Solid-Sampling High-Resolution Continuum Source Graphite Furnace Molecular Absorption Spectrometry

Solid sampling high resolution continuum source molecule absorption spectrometry (SS-HR-CS MAS) was applied for the determination of chlorine in plastic using the strontium monochloride (SrCl) molecule. For this purpose, 10?µL of 20?g L^?1 strontium (prepared from Sr(NO₃)₂) solution were pipetted with aqueous Cl standards or 0.05 to 4?mg of slivered plastic samples on a platform and introduced into the furnace. Chlorine was determined with the molecular absorption of SrCl at 635.862?nm using 1100?°C and 2200?°C for the pyrolysis and vaporization temperatures, respectively. Aqueous standards were used for calibration. The accuracy of the method was evaluated using a certified polyethylene reference material. The limit of detection and characteristic mass values of the method were 2.5?ng and 0.4?ng, respectively. The chlorine concentrations in various polyethylene beverage containers were determined.     

Nucleophilic attack by bromide ions as a first step of conversion of Se(VI) to Se(IV)

Numerous commonly used analytical methods allow only determination of a total amount of selenium in a given sample. Electroanalytical methods as well as those based on hydride generation or on formation of piazselenol allow only determination of Se(IV). To determine Se(VI) by these procedures, present alone or in mixtures with Se(IV), it is first necessary to convert Se(VI) to Se(IV). Such conversion is effective in the presence of excess of halides in acidic media or by photoreduction. In the often used conversion of Se(VI) in the presence of chlorides or less frequently of that of bromides, it has been assumed that the halide ion acts as a reducing agent. Kinetic studies of conversion of Se(VI) in acidic solutions containing an excess of bromide ions indicated that the rate determining first step of the reaction with Se(VI) is a nucleophilic substitution of the OH₂⁺ group in the protonated form of H₂SeO₄ by bromide ions. For the overall reaction with rate −d[Se(VI)]/dt = k₁[H⁺][Br⁻]^1.15[Se(IV)] the rate constant 1 × 10⁻³ L² mol⁻² s⁻¹ was found. The following formation of Se(IV) from the bromo derivative is a fast reaction probably resulting in elimination of HBrO.     

Photon transmission technique for studying multiple phase transitions in a liquid crystal

A photon transmission technique was used to monitor the multiple phase transitions in a 4-butoxyphenyl4(')-declyoxybenzoate (BOPDOB) liquid crystal. Drastic decreases in the transmitted photon intensity (I) were attributed to the sequential phase transitions in BOPDOB upon cooling. In this paper, it is assumed that the order parameter rho is proportional to the transmitted photon intensity. The isotropic-nematic and nematic-smectic-A transitions were observed and found to be of first order. It was observed that the smectic-A-smectic-C and smectic-C-smectic-G transitions are second order. It was found that for the smectic-A-smectic-C transition, critical exponent crosses over from beta=0.513+/-0.006, which is consistent with mean-field theory, to beta=0.35+/-0.009, which is consistent with heliumlike behavior, as the Ginzburg criterion predicts. The critical exponent for the smectic-C-smectic-G transition was found to be beta=0.703+/-0.001. Transition temperatures were established at each phase transitions and found to be 84.92 degrees C, 74.85 degrees C, 52.96 degrees C, and 33.03 degrees C for isotropic-nematic, nematic-smectic-A, smectic-A-smectic-C and, smectic-C-smectic-G transitions, respectively.