Fibre stability in anisotropic matrix at small strains

As acknowledged in almost all monographs on the fracture of composite materials, one of the major fracture mechanism in unidirectional fibrous composites under uniaxial compression along the reinforcing elements is the stability loss of the material structure (the structural instability). According to this mechanism, theoretical investigations of the fracture along the fibres are reduced to those of the stability loss in the material structure, and the value of external critical forces is accepted as the value of failure forces. At present, numerous theoretical investigations have been carried out in this field with the use of the three-dimensional linearized theory of stability in the framework of the piecewise-homogeneous body model. However, in all the investigations it is assumed that the matrix and the fibre material are isotropic. It is evident that in many cases it is necessary to take into account the anisotropy of the matrix material when investigating the stability loss of fibres. In view of the above, in the framework of the piecewise-homogeneous body model using the three-dimensional linearized theory of stability, the present paper considers the stability loss of the fibre in the anisotropic (transversally isotropic) matrix. The effect of the properties of the matrix material on the critical values of the external loading is examined.Submitted to the 10th International Conference of Mechanics of Composite Materials (Riga, April 20–23, 1998).Published in Mekhanika Kompozitnykh Materialov, Vol. 33, No. 5, pp. 603–611. September–October, 1997.     

Diffusion-limited annihilation in inhomogeneous environments

We study diffusion-limited (on-site) pair annihilation A + A → 0 and (on-site) fusion A + A → A which we show to be equivalent for arbitrary space-dependent diffusion and reaction rates. For one-dimensional lattices with nearest neighbour hopping we find that in the limit of infinite reaction rate the time-dependent n-point density correlations for many-particle initial states are determined by the correlation functions of a dual diffusion-limited annihilation process with at most 2n particles initially. Furthermore, by reformulating general properties of annihilating random walks in one dimension in terms of fermionic anticommutation relations we derive an exact representation for these correlation functions in terms of conditional probabilities for a single particle performing a random walk with dual hopping rates. This allows for the exact and explicit calculation of a wide range of universal and non-universal types of behaviour for the decay of the density and density correlations.     

Theory of Non-Equilibrium Stationary States as a Theory of Resonances

We study a small quantum system (e.g., a simplified model for an atom or molecule) interacting with two bosonic or fermionic reservoirs (say, photon or phonon fields). We show that the combined system has a family of stationary states parametrized by two numbers, T ₁ and T ₂ (‘reservoir temperatures’). If T ₁ ≠ T ₂, then these states are non-equilibrium stationary states (NESS). In the latter case we show that they have nonvanishing heat fluxes and positive entropy production and are dynamically asymptotically stable. The latter means that the evolution with an initial condition, normal with respect to any state where the reservoirs are in equilibria at temperatures T ₁ and T ₂, converges to the corresponding NESS. Our results are valid for the temperatures satisfying the bound min (T ₁,T ₂) > g ^{2 + α}, where g is the coupling constant and 0 < α < 1 is a power related to the infra-red behaviour of the coupling functions. Submitted: March 20, 2006. Revised: March 19, 2007. Accepted: May 11, 2007. Marco Merkli: Partly supported by an NSERC PDF, the Institute of Theoretical Physics of ETH Zürich, Switzerland, the Departments of Mathematics of McGill University and the University of Toronto, Canada. Matthias Mück: Supported by DAAD under grant HSP III. Israel Michael Sigal: Supported by NSERC under grant NA7901.     

The excited states of pyrazine: A basis set study

Summary Multiconfigurational second order perturbation theory (CASSCF/CASPT2) has been used to investigate the dependence of computed valence excitation energies and transition moments on the basis sets. Pyrazine has been selected as the test molecule. Atomic normal orbital (ANO) type basis sets are used throughout. Contractions of the structure (4s3p1d/2s) are found to be an optimal compromise between the quality and the size of the calculations and are capable of yielding results virtually identical to more extended basis sets.     

An upper bound for the largest eigenvalue of a graph: Effect of types of vertices

A novel method, based on the topology of the cardinal vertex, is described to find an upper bound for the largest eigenvalue of a graph.     

Temperature dependence of magnetization in nanocrystalline FeCoZr alloy

The temperature dependence of magnetization of a nanocrystalline Fe₆₀Co₃₀Zr₁₀ alloy annealed at various temperatures to varying crystal sizes was investigated down to 5 K in the field range up to 5 T. The fitting procedure gave T^3/2 as the leading term irrespective of the crystal size. We suggest that the increase of the coefficient by this term for smaller crystals may be connected to an increased relative volume of their surface.     

Complexes of 2,2′,2″-Nirtilotriphenol. Part IV. Cage Compounds with Phosphorus(III) and Phosphorus(V)

The ligand 2,2′,2″-nitrilotriphenol reacts with P(III) and P(V) compounds to form corresponding phosphorus complexes. Syntheses and NMR data of 2,2′,2″-nitrilotriphenyl phosphite ( II ), 2,2′,2″-nitrilotriphenyl phosphate ( III ) and of a hydrolysis product of II , 2,2′-[N-(2-hydroxyphenyl)imino]diphenly phosphonate ( IV ), are reported, as well as crystal structures of II and IV . Phosphite II shows a bicycloundecane framework; no N?Pinteraction is present. The phosphonate IV shows two coordinated and one dangling phenol group; the N-atom does not interact with the P-atom. Strong acids protonate II as well as III to form cations: in these, NMR evidence indicates coordination of the N-atom to the P-atom.     

Synchronization Analysis of Coupled Noncoherent Oscillators

We present two different approaches to detect and quantify phase synchronization in the case of coupled non-phase coherent oscillators. The first one is based on the general idea of curvature of an arbitrary curve. The second one is based on recurrences of the trajectory in phase space. We illustrate both methods in the paradigmatic example of the R?ssler system in the funnel regime. We show that the second method is applicable even in the case of noisy data. Furthermore, we extend the second approach to the application of chains of coupled systems, which allows us to detect easily clusters of synchronized oscillators. In order to illustrate the applicability of this approach, we show the results of the algorithm applied to experimental data from a population of 64 electrochemical oscillators.     

Optical and neutron domain structure studies of amorphous ribbons

The domain configuration of amorphous ribbons with positive, vanishing and negative magnetostriction constant λ_s has been investigated by means of the longitudinal magneto-optical Kerr-effect and a three-dimensional neutron depolarization analysis. The influence of an external tensile stress on the domain arrangement depends on the sign and the magnitude of the magnetostriction constant and could be measured quantitatively in the depolarization experiment. With the aid of the optical observations domain models have been established; these models were tested and completed by means of an analytic calculation of the corresponding depolarization matrix and a comparison with experimental data. Domain reorientation processes within the ribbons under an imposed tensile stress were found to agree with theoretical predictions. The nearly nonmagnetostrictive alloys shows neither stripe domains nor simple wide domains but a more complicated structure with several layers of domains.