Coherence and incoherence in extended broad band triplet interaction

In the present analysis we study the transition from coherent to incoherent dynamics in a nonlinear triplet of broad band combs of waves. Expanding the analysis of previous works, this paper investigates what happens when the band of available modes is much larger than that of the initial narrower combs within which the nonlinear interaction is not subjected to selection rules involving wave momenta. Here selection rules are present and active, and we examine how and when coherence can be defined.Comment: 6 pages, 2 figure

Chaos and a Resonance Mechanism for Structure Formation in Inflationary Models

We exhibit a resonance mechanism of amplification of density perturbations in inflationary mo-dels, using a minimal set of ingredients (an effective cosmological constant, a scalar field minimally coupled to the gravitational field and matter), common to most models in the literature of inflation. This mechanism is based on the structure of homoclinic cylinders, emanating from an unstable periodic orbit in the neighborhood of a saddle-center critical point, present in the phase space of the model. The cylindrical structure induces oscillatory motions of the scales of the universe whenever the orbit visits the neighborhood of the saddle-center, before the universe enters a period of exponential expansion. The oscillations of the scale functions produce, by a resonance mechanism, the amplification of a selected wave number spectrum of density perturbations, and can explain the hierarchy of scales observed in the actual universe. The transversal crossings of the homoclinic cylinders induce chaos in the dynamics of the model, a fact intimately connected to the resonance mechanism occuring immediately before the exit to inflation.Comment: 4 pages. This essay received an Honorable Mention from the Gravity Research Foundation, 1998-Ed. To appear in Mod. Phys. Lett.

Multipartite Entanglement Signature of Quantum Phase Transitions

We derive a general relation between the non-analyticities of the ground state energy and those of a subclass of the multipartite generalized global entanglement (GGE) measure defined by T. R. de Oliveira et al. [Phys. Rev. A 73, 010305(R) (2006)] for many-particle systems. We show that GGE signals both a critical point location and the order of a quantum phase transition (QPT). We also show that GGE allows us to study the relation between multipartite entanglement and QPTs, suggesting that multipartite but not bipartite entanglement is favored at the critical point. Finally, using GGE we were able, at a second order QPT, to define a diverging entanglement length (EL) in terms of the usual correlation length. We exemplify this with the XY spin-1/2 chain and show that the EL is half the correlation length.Comment: Published version. Incorporates correction made in erratu

Genuine Multipartite Entanglement in Quantum Phase Transitions

We demonstrate that the Global Entanglement (GE) measure defined by Meyer and Wallach, J. Math. Phys. 43, 4273 (2002), is maximal at the critical point for the Ising chain in a transverse magnetic field. Our analysis is based on the equivalence of GE to the averaged linear entropy, allowing the understanding of multipartite entanglement (ME) features through a generalization of GE for bipartite blocks of qubits. Moreover, in contrast to GE, the proposed ME measure can distinguish three paradigmatic entangled states: $GHZ_{N}$, $W_{N}$, and $EPR^{\otimes N/2}$. As such the generalized measure can detect genuine ME and is maximal at the critical point.Comment: 4 pages, 3 figures. Replaced with final published versio

The mechanism for the electrooxidation of procarbazine pharmaceutical preparation in alkaline media and its mathematical description

The mechanism for the electrooxidation of procarbazine in alkaline media has been proposed. The process is realized completely on the electrode surface and is adsorption-controlled. The oscillatory behavior in this case is more probable, than for neutral media and may be caused by influences of electrochemical oxidation and salt dissolution from the electrode surface