The size of the inner water cavity of reversed micelles formedin a triple system water-surfactant-organic solventcan be widely varied by changing the degree of surfactant hydration.This gives grounds to use reversed micelles as matrix microreactorsfor the design of supramolecular complexes of proteins. Usingultracentrifugation analysis, it has been demonstrated thatthe oligomeric composition of various enzymes (ketoglutaratedehydrogenase, alkaline phosphatase, lactic dehydrogenase, glyceraldehyde-3-phosphatedehydrogenase) solubilized in reversed micelles of Aerosol OT[sodium bis(2-ethylehexyl)sulfosuccinate] in octane changesupon variation of the degree of hydration. An oligomeric complexforms under conditions when the radius of the micelle innercavity is big enough to incorporate this complex as a whole.At lower degrees of hydration the micelles uncouplesuch complexes to their components. The catalytic propertiesof various oligomeric complexes have been studied. Possibilitiesof using reversed micelles for the separation of subunits ofoligomeric enzymes under non-denaturating conditions have beendemonstrated. In particular, the isolated subunits of alkalinephosphatase, lactic dehydrogenase and glyceralde-hyde-3-phosphatedehydrogenase have been found to be active in Aerosol OT reversedmicelles. The dependences of the catalytic activity of oligomericenzymes represent saw-like curves. The maxima of the catalyticactivity observed at these curves relate to the functioningof various oligomeric forms of an enzyme. The radii of the micelleinner cavity under conditions when these maxima are observedcorrelate with the linear dimensions of the enzyme oligomericforms. Correlation of the position of a maximum with the shapeof an oligomeric complex is discussed. 相似文献
Hydrogen may be effectively utilized as a production atmosphere in hardening of 03Kh12N10MT steel for the purpose of a directed change in phase composition, an increased quantity of residual austenite. Without reducing the strength and plasticity this makes it possible to reduce the hydrogen permeability and increase the fracture toughness of the steel, important characteristics of its effectiveness in aggressive media.
2.
For 07Kh16N6 steel heat treatment in a hydrogen atmosphere is ineffective.
Voronezh Polytechnic Institute. Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 11, pp. 25–26, November, 1991. 相似文献
This paper presents a function approximation technique based immersion and invariance adaptive controller for chaos synchronization between nonidentical systems with unknown dynamics. In the proposed control scheme, the control system is reconstructed as the combination of a controllable linear system and a variation term from the original system. The variation term is treated as time-varying uncertainty and approximated by a group of weighted chosen basis functions. The immersion and invariance methodology is employed to design the adaptive control law such that both the synchronization error and uncertainty estimation error converge to zero. Two typical chaos synchronization problems are used in numerical simulations to verify the effectiveness and superiority of the proposed controller.
Comparative data on the molecular weight distribution of polymers obtained by polymerization of ethylene, propylene and 1-hexene, and copolymerization of ethylene with α-olefins over the titanium-magnesium catalysts (TMC) in the absence and presence of hydrogen are presented. In contrast to the ethylene polymerization, in the cases of propylene and 1-hexene polymerization and copolymerization of ethylene with α-olefins, the hydrogen addition is characterized by noticeable narrowing of the molecular weight distribution (MWD) due to lower contribution of the MWD component with high molecular weight. This result is an evidence of the increased reactivity of TMC active sites producing high molecular weight poly-α-olefins and copolymers of ethylene with α-olefins in the chain transfer reaction with hydrogen. It is suggested that the increased reactivity of these sites in the transfer reaction with hydrogen appears after the 2,1-addition of α-olefin to the growing polymer chain. 相似文献
We introduce and solve a problem motivated by integrity verification in third-party data distribution: Given an undirected tree, find a minimum-cardinality set of simple paths that cover all the tree edges and, secondarily, have smallest total path lengths. We give a linear time algorithm for this problem. 相似文献
Hot stage optical and scanning electron microscopy were used to study isothermal crystallization of isotactic polypropylene (iPP) in the presence of polyimide (Pl) fibres. Under the same crystallization conditions, the occurrence of transcrystallization depends on the type of fibre used. The transcrystalline interphase has a composed structure, with a characteristic layer adjacent to the fibre surface. The layer is about 1 m thick and has a crosshatched lamellar morphology. At the interface between iPP and the Pl fibre which causes transcrystallization, the nuclei from which the transcrystalline zone grows is observed. The nuclei consist of sheaves of closely packed parallel needleshaped lamellae of uniform thickness. The transcrystallization phenomenon can be explained by the epitaxial crystallization of iPP matrix on the surface fragments (domains) formed by extended chains of Pl fibres. Different abilities of Pl fibres to induce transcrystallization are associated with the superficial morphology of the fibres.Presented in part at the 28th Europhysics Conference on Macromolecular Physics, Transitions in Oligomer and Polymer Systems, 27 September–1 October 1993, Ulm, Germany. 相似文献
The structure, phase composition, and thermal stability of the industrial zirconium alloys, namely, E110 (Zr–1% Nb) and E635 (Zr–1% Nb–0.3% Fe–1.2% Sn), which are subjected to high‐pressure torsion (HPT) at room temperature (RT), 200, and 400 °С have been studied. HPT of Zr‐alloys at RT (10 revolutions) leads to the formation of grain–subgrain nano‐sized structure and to increase the microhardness by 2.1…2.8 times. The increase in the HPT temperature to 200–400 °С leads to the increase in the structural‐element average size. The structural‐element size in the complexly alloyed E635 alloy in all cases is lower compared with the E110 alloy. The hardening of the alloys after HPT at RT and 200 °С is close, and at 400 °С is much less. HPT initiates the α‐Zr → (ω‐Zr + β‐Zr) transformation, which is the main factor for alloys hardening. The α‐Zr → (ω‐Zr + β‐Zr) transformation in the E635 alloy occurs less quickly. The maximum amount (ω‐Zr + β‐Zr) phase in the structure of the alloys is observed after HPT at RT and 200 °C, and the minimum ? at 400 °C. During heating, the alloys undergo the reverse (ω‐Zr + β‐Zr) → α transformation which depends on both the alloy composition and HPT temperature. 相似文献