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61.
S. V. Ivanov V. V. Trachevskii O. S. Titova L. A. Zozulya 《Russian Journal of Applied Chemistry》2006,79(10):1712-1714
Experimental data demonstrate that a study of accelerated aging can enable prognostication of the working capacity and storage life of polymeric formulations used in aircraft components on the basis of changes in thermogravimetric constants of these polymeric formulations. 相似文献
62.
V. B. Larin 《Ukrainian Mathematical Journal》1989,41(5):532-538
Translated from Ukrainskii Matematicheskii Zhurnal, Vol. 41, No. 5, pp. 615–621, May, 1989. 相似文献
63.
64.
Phase synchronization in a system of three virtual-cathode microwave oscillators (vircators) simulated by coupled van der Pol oscillators is studied. The phasing dynamics of the vircators is visualized with the phase portraits of the system in the triangular coordinates. Different phasing conditions are found. 相似文献
65.
V. A. Zayats A. N. Nikolaevskii T. A. Filippenko O. P. Kniga G. A. Tikhonova 《Russian Journal of Applied Chemistry》2006,79(10):1651-1654
Specific features of the initiated oxidation of polyethylene and its low-molecular-weight analogue tridecane, associated with the occurrence of the process in the short-chain mode, were studied. 相似文献
66.
67.
In this paper, we study the consistency of a variant of fractionalstep Runge–Kutta methods. These methods are designed tointegrate efficiently semi-linear multidimensional parabolicproblems by means of linearly implicit time integration processes.Such time discretization procedures are also related to a splittingof the space differential operator (or the spatial discretizationof it) as a sum of simpler linear differentialoperators and a nonlinear term. 相似文献
68.
69.
The sub-millisecond protonation dynamics of the chromophore in S65T mutant form of the green fluorescent protein (GFP) was
tracked after a rapid pH jump following laser-induced proton release from the caged photolabile compoundo-nitrobenzaldehyde. Following a jump in pH from 8 to 5 (which is achieved within 2 μs), the fluorescence of S65T GFP decreased
as a single exponential with a time constant of ∼90 μs. This decay is interpreted as the conversion of the deprotonated fluorescent
GFP chromophore to a protonated non-fluorescent species. The protonation kinetics showed dependence on the bulk viscosity
of the solvent, and therefore implicates bulk solvent-controlled protein dynamics in the protonation process. The protonation
is proposed to be a sequential process involving two steps: (a) proton transfer from solvent to the chromophore, and (b) internal
structural rearrangements to stabilize a protonated chromophore. The possible implications of these observations to protein
dynamics in general is discussed 相似文献
70.