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181.
Thermally stimulated discharge (TSD) currents of polyvinyl butyral (PVB) thin films grown on glass substrates by isothermal immersion technique have been studied as a function of the polarization field, (750 to 25000 V/cm) and iodine doping concentration (0.5 to 0.9 g/100 ml of PVB solution). Polarized PVB films exhibit two glow discharge peaks, β – at 350 °K and α – at 430 °K corresponding to activation energies of 0.19 and 0.53 eV, respectively. It has been observed that the β-peak disappears at low polarizing fields (≈︁750 V/cm). The α-peak is attributed to the depolarization of the aligned dipoles connected to the main chain whereas the β-peak arises due to the local motion or twisting of the side groups connected to main chain. On doping with iodine, both unpolarized and polarized films exhibit TSD currents. This is attributed to the formation of charge transfer complexes between iodine and PVB chains where the dipoles may be aligned due to electrostatic interaction between the charge complexes. The disappearance of the β-peak at high field (≈︁10 kV/cm) in sharp contrast to the increasing and shifting to lower temperatures of the α-peak show that the complexes are formed with the side groups of the main chain. These conclusions regarding the charge complex formation have been further confirmed by UV and infrared optical absorption data on pure and doped PVB films. 相似文献
182.
A series of (CaxSr1–x)S:Cu, Nd electroluminophors is synthesized by reducing a charge consisting of appropriate amounts of CaSO4, SrSo4, and activators. The EL mechanism is believed to be of acceleration—collision type. None of the voltage—brightness relations described in the literature is found to describe the results exactly. Frequency, temperature dependence of brightness, and brightness waves are also studied. It is observed that peak emission at about 5400 Å for SrS:Cu remains unaffected by incorporation of Nd3+ or by increasing concentration of CaS in the SrS:Cu, Nd matrix. A detailed discussion of the results is given. 相似文献
183.
Thermal chemical vapor deposition of fluorinated carbon thin films in the polymeric form is described by hot filament decomposition of the gaseous C3F6O precursor. Decomposition at filament temperatures, ≤450 °C produces films in the ordered (CF2)2n polymeric chain structure as in a tetrafluoroethylene polymer. A composite of (CF2)2n chains structure and crosslinked m(C:Fx)n phases are formed in films deposited at filament temperature ≥600 °C. Polymerization of :CF2 radicals results in (CF2)2n chain structure and the crosslinked phase emerges from a separate process involving reaction among the CF3, CFO and CF3CO radicals and including CF2. Substrate temperature affects both the C-to-F bonding configuration and the relative ratio of the composite phases. Dominant C–CF bonding structure in the low (<-5 °C) substrate temperature films is thermally less stable compared to the C–F structure, which dominates the crosslinked structure in films deposited at high (∼70 °C) substrate temperatures. Dielectric properties of the composite films are studied using the electrical equivalent model and a correlation with the C-to-F bond structure is established. High polymeric (CF2)2n phase determines the electrical impedance and the dielectric constant of the film, and the crosslinked phase imparts structural stability. PACS 81.15.Gh; 73.61.Ph; 77.84.Jd; 79.60.Fr 相似文献
184.
S. C. Rastogi 《Acta Mathematica Hungarica》1988,52(3-4):239-247
185.
Ashok Kumar Rastogi Alok Banerjee Manju Tewari Dhirendra Bahadur 《Phase Transitions》2013,86(1-2):123-130
Abstract Besides investigating a number of oxides of the series La2?xMxCuO4 (M=Ba, Pb, Sr), we have, in this investigation emphasised on the studies of the effect of annealing conditions on superconducting properties of composition La1.8Sr0.2CuO4. The effect is remarkable and is di'scuss'ed in the light of X-ray diffraction results. These samples, studied after a gap of two months, showed interesting changes which has been discussed in the present paper. 相似文献
186.
Segmented cladding fiber (SCF) is capable of single mode operation over an extended range of wavelengths while maintaining large mode area. In this paper we report the design of an SCF with mode area as large as 1,825 $\upmu \hbox {m}^{2}$ , suitable for delivery of high peak power femtosecond laser pulses at 1550 and 1064 nm wavelengths. An SCF with such a large-mode area is a few-moded fiber and its design requires careful choice of design parameters to have robustness against mode-coupling effects and bend loss. In this paper we address these issues and report a design of an SCF showing near distortion-free propagation of 100-fs, 53-kW peak power pulses at 1550-nm wavelength with 1,825- $\upmu \hbox {m}^{2}$ mode area through fundamental mode. The same fiber can also deliver 250-fs, 15-kW peak power pulses at 1064-nm wavelength with 1,793- $\upmu \hbox {m}^{2}$ mode area. The fiber has been analyzed by using the radial effective-index method in conjunction with transfer matrix method and the pulse propagation has been studied by solving the nonlinear Schroedinger equation by split-step Fourier method. Such a fiber would find applications in multiphoton microscopy and in biomedical engineering. 相似文献
187.
Shiva K. Rastogi Robert A. Rogers Justin Shi Christopher T. Brown Cindy Salinas Katherine M. Martin Jacob Armitage Christopher Dorsey Gao Chun Peter Rinaldi William J. Brittain 《Magnetic resonance in chemistry : MRC》2016,54(2):126-131
We report through‐space (TS) 19F–19F coupling for ortho‐fluoro‐substituted Z ‐azobenzenes. The magnitude of the TS‐coupling constant (TSJFF) ranged from 2.2–5.9 Hz. Using empirical formulas reported in the literature, these coupling constants correspond to non‐bonded F–F distances (dFF) of 3.0–3.5 Å. These non‐bonded distances are significantly smaller than those determined by X‐ray crystallography or density functional theory, which argues that simple models of 19F–19F TS spin–spin coupling solely based dFF are not applicable. 1H, 13C and 19F data are reported for both the E and Z isomers of ten fluorinated azobenzenes. Density functional theory [B3YLP/6‐311++G(d,p)] was used to calculate 19F chemical shifts, and the calculated values deviated 0.3–10.0 ppm compared with experimental values. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
188.
Radhey M. Naik Surendra Prasad Shiv B. S. Yadav R. Rastogi R. K. Tiwari 《国际化学动力学杂志》2012,44(6):398-406
The kinetics and mechanism of the formation of an antitubercular complex [Fe(CN)5(INH)]3? based on the substitution reaction between K4[Fe(CN)6] and isoniazid (INH), i.e., isonicotinohydrazide, catalyzed by Hg2+ in aqueous medium was studied spectrophotometrically at 435 nm (the λmax of the golden‐yellow‐colored complex [Fe(CN)5(INH)]3?) as a function of pH, ionic strength, temperature, and the concentration of the reactants and the catalyst. The replacement of coordinated CN? in [Fe(CN)6]4? was facilitated by incoming ligand INH under the optimized reaction conditions: pH 3.5 ± 0.02, temperature = 30.0 ± 0.1°C, and ionic strength I = 0.05 M (KNO3). The stoichiometry of the reaction and the stability constant of the complex ([Fe(CN)5(INH)]3?) have been established as 1:1 and 2.10 × 103 M, respectively. The rate of catalyzed reaction was found to be slow at low pH values, to increase with increasing pH, to attain a maximum value at 3.50 ± 0.02, and finally to decrease after pH > 3.5 due to less availability of H+ ions needed to regenerate the catalytic species. The initial rates were evaluated for each variation from the absorbance versus time curves. The reaction was found to be pseudo‐first order with respect to [INH] and first order with respect to [Fe(CN)64?] at lower concentration, whereas it was found to be fractional order at higher [INH] and [Fe(CN)64?]. The ionic strength dependence study showed a negative salt effect on the rate of the reaction. Based on experimental results, a mechanism for the studied reaction is proposed. The rate equation derived from this mechanism explains all the experimental observations. The evaluated values of activation parameters for the catalyzed reaction suggest an interchange dissociative (Id) mechanism. © 2012 Wiley Periodicals, Inc. Int J Chem Kinet 44: 398–406, 2012 相似文献
189.
We discuss a class of solids which have in their structure fairly separated tetrahederal clusters of transition metals: vanadium and molybednum. With decreasing temperature these compounds undergo a structural transition from cubic to rhombohederal phase at a temperature T s , followed by a transition to a ferromagnetic phase at a lower temperarure T c . Magnetic measurements indicate the presence of moments of spin half per cluster. Between T c and T s susceptibility shows large departures from Curie-Weiss behavior and specific heat has an unusually large non-phononic contribution. We present a model in which each cluster acts as a unit associated with a magnetic moment of spin half and a structural degree of freedom related to distortions of the tetrahedron. Our model accounts for all the observed features including effects due to external pressure and magnetic field.https://doi.org/10.1209/0295-5075/101/67008 相似文献
190.
S. C. Rastogi 《Chromatographia》1990,29(1-2):13-15
Summary A gas chromatographic (GC) method for the routine analysis of fully halogenated chlorofluorocarbons (CFCs) in aerosol cans is described. The identification of CFCs by GC was found to be in full agreement with those by GC-mass-spectrometery. The method has been applied to the analysis of CFCs in 448 aerosol products. The most commonly used fully halogenated CFC propellants in aerosol cans were found to be CFC11, CFC12 and CFC114. 相似文献