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191.
On the basis of a complex null-polarimetric method, the natural birefringence and the rotation of the optical indicatrix in crystals of deuterated triglycinesulfate are measured in the temperature range of 300–340 K. The temperature-dependent behavior of the optical parameters is shown to be close to that observed previously in triglycinesulfate crystals. Changes in them upon the ferroelectric phase transition can be accounted for by the spontaneous quadratic electro-optic effect, with the values of the electro-optic coefficients being larger by a factor of 1.4 than in triglycinesulfate crystals.  相似文献   
192.
The initial-boundary-value problem for the equations describing motion of a thin, medium-length, non-circular cylindrical shell is examined. The shell edges are not necessarily plane curves, with the conditions of a joint support, a rigid clamp or a free edge being considered as the boundary conditions. The shell is supposed to experience normal internal (or external) dynamic pressure which may be non-uniform in the circumferential direction. It is assumed that the initial displacements and velocities of the points at the shell middle surface are functions decreasing rapidly away from some generatrix. Using the complex WKB method the asymptotic solution of the governing equations is constructed by superimposing localized families (wave packets) of bending waves running in the circumferential direction. The dependence of frequencies, group velocities, amplitudes and other dynamic characteristics upon variable pressure and geometrical parameters of the shell are studied. As an example, the wave forms of motion of a circular cylindrical shell with sloping edges under growing dynamic pressure are considered. The effect of localization of bending vibrations near the longest generator as well as the effects of reflection, focusing and increasing amplitude in the running wave packets are revealed.  相似文献   
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The tendency of boron-containing, iron-based glasses to show non monotonic changes of Curie Temperature (T c ) and room temperature saturation magnetization (SM) was examined by magnetic measurements and Mossbauer spectroscopy. Depending on B/Fe ratio theT c and SM first increased up to a maximum value and then steadily decreased, probably because of a shortrange ordering, due to the strong chemical interaction between iron and boron atoms, leading iron atoms in vicinity with Fe-atoms rather than another TM-atom. Finally, the phenomenon becomes analogous to the order-disorder phenomenon in crystalline alloys. An observed unusual crystallization behaviour, consisting of heterogeneous nucleation, was also ascribed to this ordering, which leads to the formation of associations, acting as the first nuclei of crystallization.  相似文献   
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A series of novel multifunctional hydrogels that combined the merits of both thermoresponsive and biodegradable polymeric materials were designed, synthesized, and characterized. The hydrogels were copolymeric networks composed of N‐isopropylacrylamide (NIPAAM) as a thermoresponsive component, poly(L‐lactic acid) (PLLA) as a hydrolytically degradable and hydrophobic component, and dextran as an enzymatically degradable and hydrophilic component. The chemical structures of the hydrogels were characterized by an attenuated total reflection–Fourier transform infrared spectroscopy (ATR–FTIR) technique. The hydrogels were thermoresponsive, showing a lower critical solution temperature (LCST) at approximately 32 °C, and their swelling properties strongly depended on temperature changes, the balance of the hydrophilic/hydrophobic components, and the degradation of the PLLA component. The degradation of the hydrogels caused by hydrolytic cleavage of ester bonds in the PLLA component was faster at 25 °C below the LCST than at 37 °C above the LCST, determined by the ATR–FTIR technique. Due to their multifunctional properties, the designed hydrogels show great potential for biomedical applications, including drug delivery and tissue engineering. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5054–5066, 2004  相似文献   
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