Acoustic inspection of bond strength of steel-reinforced mortar after exposure to elevated temperatures

In order to evaluate the bond strength between the reinforcement and concrete after fire damage, a combination of acoustic through-transmission and pull-out tests were used. Previous studies have shown a 25% decrease in the ultrasonic pulse velocity at 90% of the maximum load at room temperature. The specimens were kept in the oven at an elevated temperature for 1, 2, or 3 h. They were then removed and cooled to room temperature. Inspection was conducted using a high-power ultrasonic pulse velocity system while a pull-out load was applied. The correlation between preheated temperature, acoustic wave velocity, and the applied load was analyzed. Initial results show that bond strength and pulse velocity decreased substantially as the temperature or the heating time increased.     

Comparing Diffusion Approximation with Radiation Transfer Analysis for Light Transport in Tissues

The diffusion model that is an approximation of the equation of radiation transfer is typically used to describe photon migration in scattering-dominant media. In general biological tissue is highly scattering and very weakly absorbing against near-infrared light, yet it is heterogeneous and may contain relatively highly absorbing or low-scattering regions. Here applicability of the diffusion approximation over the radiative transfer theory for describing ultrafast laser transport in biological tissues is numerically studied and investigated over different kinds of tissue conditions and geometries. Tissues having tumors of different sizes, locations and nature as well as dual-tumor and low-scattering conditions are considered. Radiation transfer analysis is taken as a comparison objective and it is initially proved to be accurate in benchmark comparisons with Monte Carlo simulation. The results predict systematically about the compatible conditions where and when we can use the diffusion approximation and the conditions in which the diffusion approximation may provide misleading results.     

Investigation of the anisotropy of the transverse magnetoresistance in single-crystal ferromagnetic films

The transverse magnetoresistance in films of nickel, iron, and several alloys is investigated when there is a current along the [100] and [110] directions as a function of the angle between the direction of the field (16 kG) and the plane of the film. The results obtained are compared with experimental data and with theory for bulk single crystals. An explanation of the anomalies observed in the film is given.Translated from Izvestiya VUZ. Fizika, No. 12, pp. 7–10, December, 1973.     

Synthesis and mesomorphic properties of three- and four-ring liquid crystals containing cyclohexyl, phenyl and pyridyl units

Two series of 4-(3-alkoxycarbonylpyridyl-6-ethynyl)phenyl trans-4-n-alkylcyclohexylcarboxylates and 4-(3-alkoxycarbonylpyridyl-6-ethynyl)phenyl 4-(trans-4-n-alkylcyclohexyl)benzoates have been prepared. Their mesmorphic properties were observed and measured by polarizing optical microscopy and differential scanning calorimetry. The relationship between structures and properties is discussed, showing that the ferroelectric phase can be observed when chiral terminal chains exist.     

Guettardine,a possible biogenetic intermediate in the formation of corynanthe-cinchona alkaloids

The structure of guettardine 1, an indole alkaloid isolated from the bark of $\text{Guettarda heterosepala}$ (Rubiaceae), was determined from an analysis of its MS, ¹H and ¹³C NMR spectral data, and by a chemical correlation with dihydrocorynantheol 7. Guettardine 1 can be considered to be an intermediate between the Corynanthé and the cinchonamine groups of alkaloids which are precursors of quinine and its derivatives.     

Kinetic flash spectroscopic study of the CH3O2?CH3O2 and CH3O2?SO2 reactions

Methylperoxy radicals were generated by the flash photolysis of azomethane–oxygen mixtures. The observed broadband spectrum of the CH₃O₂ radical is similar, but not identical to those reported previously. The CH₃O₂ decay followed second-order kinetics at high CH₃O₂ concentrations with k₄' = (2.5 ± 0.3) × 10⁸ liter/mol·sec (23 ± 2°C); 2CH₃O₂ → products (4). Because of the potential loss of CH₃O₂ through the reactions with HO₂ and CH₃O radicals subsequently formed in this system, simulations suggest that the true k₄ is in the range: 2.5 × 10⁸ ≥ k₄ ≥ 2.3 × 10⁸ liter/mol·sec. Deviations from linearity of the plot of the reciprocal of the CH₃O₂ absorbance versus time were seen at long times and were attributed to the reaction (5) with an apparent rate constant k₅' ? (1.6 ± 0.4) × 10⁵ liter/mol·sec; CH₃O₂ + Me₂N₂ → product (5). The CH₃O₂–SO₂ reaction, CH₃O₂ + SO₂ → products (16), was studied by observing CH₃O₂ decay in flashed mixtures of Me₂N₂, O₂, and SO₂. The results gave the apparent second-order rate constant k₁₆' ? (6.4 ± 1.4) × 10⁶ liter/mol·sec. It appears likely that each occurrence of reaction (5) and (16) is followed by the loss of an additional CH₃O₂ radical and that k₅ ? k₅'/2 and k₁₆ ? k₁₆'/2. Our findings suggest that a significant fraction of the SO₂ oxidation in a sunlight-irradiated NO_x?RH-polluted atmosphere, may occur by reaction with CH₃O₂ as well as from the HO and HO₂ reactions.