Levitating states of superconducting rings in the field of a fixed ring with constant current

We consider the possibility of designing a plasma trap with a magnetic system formed by super-conducting rings and coils levitating in the field of a fixed coaxial coil carrying constant current. An analytic dependence of the potential energy of such a system with one or two levitating superconducting rings having trapped preset magnetic fluxes on their coordinates in the uniform gravitational field is obtained in the thin ring approximation. Calculations performed in the Mathcad system show that equilibrium states of such a system exist for certain values of parameters. Levitating states of a single superconducting ring and two superconducting rings in the field of the coil with constant current are observed experimentally in positions corresponding to calculated values.     

Structural and magnetoelectric properties of MFe<Subscript>2</Subscript>O<Subscript>4</Subscript>–PZT (M = Ni,Co) and La<Subscript>x</Subscript>(Ca,Sr)<Subscript>1-x</Subscript>MnO<Subscript>3</Subscript>–PZT multilayer composites

Thick-film layered magnetoelectric composites consisting of ferromagnetic and ferroelectric phases have been synthesized with nickel ferrite (NFO), cobalt ferrite, La_0.7Sr_0.3MnO₃ (LSMO), or La_0.7Ca_0.3MnO₃ (LCMO) and lead zirconate titanate (PZT). Structural, magnetic, and ferromagnetic resonance characterization shows evidence for defect-free ferrites, but deterioration of manganite parameters. The resistivity and dielectric constants are smaller than expected values. The magnetoelectric effect (ME) is stronger in ferrite–PZT than in manganite–PZT. The ME voltage coefficient _E at room temperature is the highest in NFO–PZT and the smallest for LCMO–PZT. The transverse ME effect is an order of magnitude stronger than the longitudinal effect. The magnitude of _E correlates well with magnetic permeability for the ferrites. PACS 75.80.+q; 75.70.Gg; 75.60.-d     

Heat capacity of the Pb<Subscript>5</Subscript>(Ge<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Si<Subscript>x</Subscript>)<Subscript>3</Subscript>O<Subscript>11</Subscript> ferroelectric system

The temperature dependences of the molar heat capacity at constant pressure, C_p, of Pb₅(Ge_1?xSi_x)₃O₁₁ crystals with x=0, 0.39, and 0.45 in the range 5–300 K, as well as of their permittivity, dielectric losses, and the pyroelectric effect, have been measured. Experimental data on the temperature behavior of the heat capacity are presented in the form of a sum of two Debye and one Einstein terms, C_p(T)=0.405C_D1(Θ_D1=160 K, T)+0.53C_D2(Θ_D2=750 K, T)+0.046C_E(Θ_E=47 K, T). Besides a peak in the region of the ferroelectric Curie point T_c=450 K for crystals with x=0, the temperature dependences of the heat capacity did not reveal any other pronounced anomalies.     

Composition-induced transition of spin-modulated structure into a uniform antiferromagnetic state in a Bi<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>La<Subscript>x</Subscript>FeO<Subscript>3</Subscript> system studied using <Superscript>57</Superscript>Fe NMR

By analyzing the NMR line shape, the transformation of a spatially spin-modulated magnetic structure in BiFeO₃ into an ordinary spatially uniform structure of the LaFeO₃ orthoferrite in Bi_1?xLa_xFeO₃ solid solutions is studied. The measurements are made using a spin-echo technique at temperatures of 77 and 4.2 K on ceramics with compositions x=0, 0.1, 0.2, 0.61, 0.9, and 1.0 enriched by the ⁵⁷Fe isotope. It is shown that the spin-modulated structure disappears near the concentration x=0.2, which corresponds, according to the published data, to the phase transition with a change in the unit-cell symmetry R3c → C222. A formula is obtained describing the NMR absorption line shape for the spin-modulated structure with account of local line-width. Theoretical spectra adequately describe the evolution of the experimental spectrum in the concentration range 0≤x≤0.2. Highly nonuniform local magnetic fields in the intermediate compositions make it impossible to detect NMR signals in a sample with x=0.61. A uniform magnetic structure characterized by a single narrow line arises in the range of existence of a phase with the symmetry Pnma typical of the pure orthoferrite LaFeO₃.     

Synthesis of functionalized sulfonamides via 1,3-dipolar cycloaddition of pentafluorophenyl vinylsulfonate

[reaction: see text] An efficient intermolecular 1,3-dipolar cycloaddition of a variety of nitrones to pentafluorophenyl (PFP) vinylsulfonate is described. The transformation produces stable "reversed" cycloadducts of unprecedented stereo- and regioselectivity. Subsequent amine displacement of the PFP moiety furnished functionalized sulfonamide products in good yields.     

Circadian synchrony in networks of protein rhythm driven neurons

The interaction between gene activation and cellular activity has recently emerged as a critical aspect of brain behavior, but the dynamics of networks incorporating these interactions are poorly understood. An interesting phenomena arises when the genetic activation oscillates endogenously and a network of such cells synchronize to a coherent rhythm, such as is the case with the suprachiasmatic nucleus. To explain this synchronization, we propose a model in which a mRNA/protein expression cycle drives neurons electrical activity, and synaptic activation shifts the phase of the protein rhythm. Using lattice networks, we demonstrate that these interactions are sufficient to generate coherent oscillation. © 2006 Wiley Periodicals, Inc. Complexity 12: 67–72, 2006     

Nonergodicity in electron capture dissociation investigated using hydrated ion nanocalorimetry

Hydrated divalent magnesium and calcium clusters are used as nanocalorimeters to measure the internal energy deposited into size-selected clusters upon capture of a thermally generated electron. The infrared radiation emitted from the cell and vacuum chamber surfaces as well as from the heated cathode results in some activation of these clusters, but this activation is minimal. No measurable excitation due to inelastic collisions occurs with the low-energy electrons used under these conditions. Two different dissociation pathways are observed for the divalent clusters that capture an electron: loss of water molecules (Pathway I) and loss of an H atom and water molecules (Pathway II). For Ca(H(2)O)(n)(2+), Pathway I occurs exclusively for n >or= 30 whereas Pathway II occurs exclusively for n 相似文献