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981.
About 40 epoxide-amine network polymers with glass transition temperatures ranging from 0 to 232°C were investigated, about one-third being reported for the first time. The glass transition temperature Tgl of the corresponding linear copolymers was first calculated by use of an additivity law whose physical validity was carefully checked. Then the contribution of crosslink mers was determined, and various physical and empirical approaches of the effect of crosslinking on Tg were compared. The results gave evidence in favor of the DiMarzio approach. A predictive relationship based on these considerations is proposed. 相似文献
982.
983.
The mechanisms of liquid-phase phenol ozonation are revised. A new mechanism in which a significant role is played by free-radical reactions is suggested for this process. 相似文献
984.
985.
986.
987.
988.
V. I. Karpman
A. G. Shagalov
《Physics letters. A》1991,160(6):538-540The self-focusing described by the nonlinear Schrödinger equation with a higher-order derivative term is investigated numerically. We demonstrate that, depending on the sign before this term, it may lead in the final stage either to defocusing or to a steady homogeneous wave beam. In both cases the transition to the final state is shown to be oscillatory. 相似文献
989.
The arc discharge was studied in a transparent channel at an intense flow rate of nitrogen, hydrogen, air, carbon dioxide in the current range 100–1500 A. The internal diameter of the porous channel varied from 10 to 34 mm, the length - from 50 to 150 mm, the air and nitrogen flow rates - from 0.05 to 1.5 kg/s, hydrogen - from 0.005 to 0.05 kg/s. The electric field strength in the arc channel reached a value of 300 V/cm for N2 and 500 V/cm for H2. The effect of plasma thermochemical non-equilibrium was discovered. 相似文献
990.
We have studied by ESR and ENDOR spectroscopy the free radicals produced in γ-irradiated inclusion compound formed between the ketone 10-nonadecanone and urea. Only one type of long lived radical is formed by the removal of an α-proton from the ketone. The hyperfine (hf) coupling constants of the α- and β-protons of the radicals have been measured by ESR at different temperatures in the range 110–292 K and at different orientations of the crystals. The hf coupling of the γ-protons of the radical and of the urea protons have been studied by ENDOR. The temperature and angular dependences of the coupling constants have been analyzed in terms of the internal and overall motions of the radical inside the hexagonal channels formed by the urea molecules. It has been found that the radical cannot perform complete reorientations around the long molecular axis, but it undergoes restricted rotational diffusion. This process is explained by assuming a coupling between the rotational and translational degrees of freedom of the radical inside the urea channels. 相似文献