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131.
We give a short proof for the Mixed Connectivity Certificate Theorem of Even, Itkis and Rajsbaum and provide an upper bound on the edge number of a certificate of local T-mixed connectivity up to k.  相似文献   
132.
We introduce the notion of an invariant of characteristics for a system of first-order partial differential equations. We prove that the existence of invariants is connected with passiveness of some systems. We describe a few methods for construction of new invariants from those already known. We give a scheme for application of the invariants to reduction and integration of systems of partial differential equations. As an application we consider the equation of gas dynamics.  相似文献   
133.
The NixAl1−x alloys exhibit shape memory effect, for which thermoelastic phase transformations are essential, in the composition range of 60<x<65. The analytical studies are very difficult on the thermoelastic phase transformations because these types of transformations exhibit anharmonic behaviour. In order to overcome this difficulty, it is possible to benefit from the molecular dynamics (MD) calculations based on interatomic interaction potentials. In the present study, the interatomic interactions of Ni62.5Al37.5 alloy have been modelled by means of Lennard-Jones potential energy function. A MD cell of 1024 atoms in B2 super lattice has been chosen and the structural changes were investigated on this system with changing temperature. It has been observed that the model alloy exhibits the thermoelastic phase transformation with thermal cycling. A hysteresis has been determined between forward and backward transformation temperatures. The structural analysis is also done before and after the transformation.  相似文献   
134.
The dynamics of the photoinduced differential absorption and excited-state bleaching spectra of single-walled carbon nanotubes suspended in a micellar solution were studied in the spectral range from 40 to 1000 nm within a time interval from 70 fs to 150 ps under excitation by 50-fs pulses with photon energies 2 and 4 eV. The bleaching and absorption bands were observed in the spectra; the positions of the bleaching peaks were independent of the photon energy of the exciting femtosecond pulse in the range 2–4 eV. It was established that, for delay times shorter than 1 ps, the shape of the differential spectrum of excited nanotubes coincided with the shape of the second derivative of the absorption spectrum of unexcited nanotubes in the frequency range of exciting pulse above 18000 cm?1 (the range of absorption bands of metallic nanotubes). In the frequency range below 16000 cm?1 (the range of absorption peaks of semiconducting nanotubes), the bleaching peaks in the differential spectrum of excited nanotubes undergo a high-frequency shift of 200–300 cm?1 with respect to the second-derivative spectrum of unexcited nanotubes. The excited-state relaxation rate constants were measured. They are well approximated by the exponential dependences and depend on the probe-pulse wavelength. An assumption was made about the nature of the observed spectra of excited nanotubes and about the excitation relaxation.  相似文献   
135.
It was shown that nonionic surfactants (NS) can be determined by potentiometry using liquid NS-selective electrodes. The effect of medium acidity and foreign substances on the operation of liquid NS-selective electrodes was studied. Some properties of NS-selective electrodes were determined.  相似文献   
136.
The Ac behaviour of PLZT 6/80/20 ferroelectric ceramics was analyzed around and above the phase transition. Two relaxation processes are identified, showing that the so-called ‘universal relaxation law’ holds for the ceramics. A critical point in the values of the Ac conductivity, around the temperature corresponding to the maximum of the dielectric losses, is observed below the transition temperature due to the relaxor behaviour. The frequency dependence of the Ac conductivity at various temperatures and the hysteresis loops show classical relaxor behaviour with a diffuse phase transition.  相似文献   
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Background: Although microemulsion-based nanoparticles (MEs) may be useful for drug delivery or scavenging, these benefits must be balanced against potential nanotoxicological effects in biological tissue (bio-nano interface). We investigated the actions of assembled MEs and their individual components at the bio-nano interface of thrombosis and hemolysis in human blood. Methods: Oil-in-water MEs were synthesized using ethylbutyrate, sodium caprylate, and pluronic F-68 (ME4) or F-127 (ME6) in 0.9% NaClw/v. The effects of MEs or components on thrombosis were determined using thrombo-elastography, platelet contractile force, clot elastic modulus, and platelet counting. For hemolysis, ME or components were incubated with erythrocytes, centrifuged, and washed for measurement of free hemoglobin by spectroscopy. Results and conclusions: The mean particle diameters (polydispersity index) for ME6 and ME4 were 23.6 ± 2.5 nm (0.362) and 14.0 ± 1.0 nm (0.008), respectively. MEs (0, 0.03, 0.3, 3 mM) markedly reduced the thromboelastograph maximal amplitude in a concentration-dependent manner (49.0 ± 4.2, 39.0 ± 5.6, 15.0 ± 8.7, 3.8 ± 1.3 mm, respectively), an effect highly correlated (r2 = 0.94) with similar changes caused by pluronic surfactants (48.7 ± 10.9, 30.7 ± 15.8, 20.0 ± 11.3, 2.0 ± 0.5) alone. Neither oil nor sodium caprylate alone affected the thromboelastograph. The clot contractile force was reduced by ME (27.3 ± 11.1–6.7 ± 3.4 kdynes/cm2, P = 0.02, n = 5) whereas the platelet population not affected (175 ± 28–182 ± 23 106/ml, P = 0.12, n = 6). This data suggests that MEs reduced platelet activity due to associated pluronic surfactants, but caused minimal changes in protein function necessary for coagulation. Although pharmacological concentrations of sodium caprylate caused hemolysis (EC50 = 213 mM), MEs and pluronic surfactants did not disrupt erythrocytes. Knowledge of nanoparticle activity and potential associated nanotoxicity at this bio-nano interface enables rational ME design for in vivo applications.  相似文献   
140.
Hydrophosphoryl nucleophilic agents add to the CN bond of N-sulfonyltrichloroacetimidoylphosphonates to give unstable C,C-diphosphorylated adducts, which undergo competitive 1,2-C → N phosphorotropic rearrangement and dehydrochlorination with the formation of aza-Perkow reaction products, C,N-diphosphorylated dichlorovinylsulfonamides. This is the first reliably identified case of an aza-Perkow transformation for acid phosphites and their initial nucleophilic attack at the C atom of the azomethine bond in the aza-substrates.  相似文献   
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