Annealing effects on the magnetization of Co–Ni–B amorphous nanoparticles

Chemically prepared (Co_xNi_1−x)_1−yB_y (x=0.5, 0.75, 1; y≈0.4) amorphous fine particles were characterized by X-ray diffraction, DTA and TGA, and in situ magnetic measurement as a function of annealing temperature in an inert atmosphere. Magnetic measurement performed in as-prepared and 150°C annealed samples shows an increase of the saturation magnetization and magnetic moment after thermal treatment. Room temperature magnetization increases by factors of 3.5, 1.8, and 1.5, for x=0.5, 0.75, and 1, respectively. These measurements may indicate a local re-ordering of the amorphous phase at temperatures much lower than the full crystallization temperature.     

Infrared and Raman spectroscopic investigation of Eu3+-doped mono and Di-urethanesil hybrid siliceous materials

The general features of two series of sol-gel derived materials, designatedurethanesils (Ut), have been investigated by infrared and Raman spectroscopies with the goal of elucidating the chemical environment of the Eu³⁺ cations. The host frameworks of the two families of ormolytes studied have been represented by m-Ut(350) and d-Ut(300), where m stands for mono, d stands for di, 350 and 300 are the average molecular weights of the organic precursors (poly(ethylene glycol) methyl ether, PEGME, and poly(ethylene glycol), PEG, respectively). The hybrid matrix of the mono-xerogels is composed by a siliceous backbone bonded by means of urethane linkages (-NHC (=O)O-) to pendant methyl end capped oligopolymer chains with approximately 7 oxyethylene units, whereas that of the di-xerogels is based on a siliceous network grafted through urethane groups to both ends of poly(oxyethylene) segments containing about 6 (OCH₂CH₂) repeat units. Both classes of materials have been doped with europium triflate (Eu(CF₃SO₃)₃). The doped samples have been identified by m-Ut(350)_nEu(CF₃SO₃)₃ and d-Ut(300)_nEu(CF₃SO₃), where n is the molar ratio of (OCH₂CH₂) repeat units per Eu³⁺ ion. Materials with n ranging from ∞ to 5 have been analyzed. The spectral data obtained provide evidence that the cations begin to coordinate to the ether oxygen atoms of the oligopolymer chains at n=40 in the mono-urethanesils and at n=10 in the di-urethanesils. In mono-urethanesils samples with n>40 and in di-urethanesils materials with n>10, the Eu³⁺ coordinate exclusively to the carbonyl oxygen atoms of the urethane linkages. Paper presented at the 8th EuroConference on Ionics, Carvoeiro, Algarve, Portugal, Sept. 16–22, 2001.     

On the Cartan–Jacobson Theorem

The well-known Cartan–Jacobson theorem claims that the Lie algebra of derivations of a Cayley algebra is central simple if the characteristic is not 2 or 3. In this paper we have studied these two cases, with the following results: if the characteristic is 2, the theorem is also true, but, if the characteristic is 3, the derivation algebra is not simple. We have also proved that in this last case, there is a unique nonzero proper seven-dimensional ideal, which is a central simple Lie algebra of type A₂, and the quotient of the derivation algebra modulo this ideal turns out to be isomorphic, as a Lie algebra, to the ideal itself. The original motivation of this work was a series of computer-aided calculations which proved the simplicity of derivation algebras of Cayley algebras in the case of characteristic not 3. These computations also proved the existence of a unique nonzero proper ideal (which turns out to be seven-dimensional) in the algebra of derivations of split Cayley algebras in characteristic 3.     

Paraxial designing of planar waveguide variable-index focusing elements: Part 2—lenses of elliptical symmetry

A paraxial ray-optics formalism proposed for designing radially symmetric variable-index lenses is extended to the case of lenses of elliptical symmetry of the index profile.     

Continuous reaction system to investigate the dispersion polymerization of vinyl monomers in supercritical carbon dioxide

A laboratory‐scale continuous reaction system using a stirred tank reactor was assembled in our laboratory to study the dispersion polymerization of vinyl monomers in supercritical carbon dioxide (scCO₂). The apparatus was equipped with a suitable downstream separation section to collect solid particles entrained in the effluent stream from the reactor, whose monomer concentration could be measured online with a gas chromatograph. The dispersion polymerization of methyl methacrylate in scCO₂ was selected as a model process to be investigated in the apparatus. The experiments were performed at 65 °C and 25 MPa with 2,2′‐azobisisobutyronitrile as the initiator and a reactive polysiloxane macromonomer as a surfactant to investigate the effect of the mean residence time of the reaction mixture on the monomer conversion, polymerization rate, polymer molecular weight, and particle size distribution. The results were compared with those obtained in batch polymerizations carried out under similar operative conditions. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4122–4135, 2006     

Effect of the environment on the stability of surfactant–polypeptide self‐assembled complexes: Molecular dynamics simulations of stoichiometric complexes formed by N‐dodecyltrimethylammonium and poly(α,L‐glutamate) in chloroform,methanol, and water

A series of molecular dynamics simulations have been performed to study the supramolecular structure of self‐assembled complexes formed by N‐dodecyltrimethylammonium cations and the synthetic polypeptide poly(α,L ‐glutamate). The influence of the type of solvent has been investigated, considering explicit environments of chloroform, water, and methanol on a stoichiometric complex containing 15 residues. In chloroform, the complex stabilizes in a regular structure: the polypeptide adopts an α‐helix conformation that is regularly surrounded by surfactant molecules to form electrostatic interactions through a multiple interaction pattern. However, this structure destabilizes in methanol and water: (a) the α‐helix unfolds in the two solvents and (b) the electrostatic links between the surfactant molecules and the polyanion are disrupted in aqueous solution, although these interactions are still preserved in methanol. The role of the solvent environment in stabilizing or destabilizing the polypeptide secondary structure, the organization of the surfactant molecules, and predominantly the surfactant–polypeptide supramolecular organization is discussed in detail. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1122–1133, 2006     

Diff (S 1) and the Teichmüller spaces

Precisely two of the homogeneous spaces that appear as coadjoint orbits of the group of string reparametrizations, , carry in a natural way the structure of infinite dimensional, holomorphically homogeneous complex analytic Kähler manifolds. These areN=Diff(S ¹)/Rot(S ¹) andM=Diff(S ¹)/Möb(S ¹). Note thatN is a holomorphic disc fiber space overM. Now,M can be naturally considered as embedded in the classical universal Teichmüller spaceT(1), simply by noting that a diffeomorphism ofS ¹ is a quasisymmetric homeomorphism.T(1) is itself a homomorphically homogeneous complex Banach manifold. We prove in the first part of the paper that the inclusion ofM inT(1) iscomplex analytic.In the latter portion of this paper it is shown that theunique homogeneous Kähler metric carried byM = Diff (S ¹/SL(2, ) induces preciselythe Weil-Petersson metric on the Teichmüller space. This is via our identification ofM as a holomorphic submanifold of universal Teichmüller space. Now recall that every Teichmüller spaceT(G) of finite or infinite dimension is contained canonically and holomorphically withinT(1). Our computations allow us also to prove that everyT(G), G any infinite Fuchsian group, projects out ofM transversely. This last assertion is related to the fractal nature ofG-invariant quasicircles, and to Mostow rigidity on the line.Our results thus connect the loop space approach to bosonic string theory with the sum-over-moduli (Polyakov path integral) approach.     

Divisible modules and space of divisibility of an integral domain

Sunto Se A è un modulo divisibile su un dominio d'integrità R e Q è il campo delle frazioni di R, sia R_A Q il massimo sopraanello di R tale che A possa essere dotato della struttura di R_A-modulo. La struttura di R_A riflette quella di A. Se A è un modulo divisibile semplice di torsione, cioè è divisibile di torsione e non ha sottomoduli divisibili propri non nulli, R_A è analiticamente irriducibile. Se C e D sono due moduli divisibili semplici, diciamo C equivalente a D se R_C=R_D. Se d-Space (R) è un insieme di rappresentanti delle classi di equivalenza degli R-moduli divisibili semplici, d-Space (R) puó essere dotato di una struttura di spazio di Hausdorff zero-dimensionale; lo spazio topologico d-Space (R) (da noi chiamato lo spazio di divisibilità di R) contiene un sottospazio chiuso omeomorfo alla superficie di Riemann astratta di R dotata della patch topology.

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Lavoro eseguito con il contribute del Ministero délia Pubblica Istruzione     

Stationary axisymmetric solutions in the vacuum Jordan-Brans-Dicke theory

It is shown that any stationary axisymmetric solution to the vacuum field equations of the Jordan-Brans-Dicke (JBD) theory may be obtained from a composition of any stationary axisymmetric vacuum Einstein spacetime with the Weyl class of metrics. Thus, generating solution techniques can be used to obtain any stationary axisymmetric JBD vacuum solution. In this manner, C. B. G. McIntosh's results concerning this topic are improved upon.