XMCD studies of magnetic polarization at Mo atoms in CoMo alloy and magnetically coupled Co/Mo multilayers

Magnetic polarization of Mo atoms in Co₉₆Mo₄ alloy film and Co/Mo multilayered structures has been studied by X‐ray magnetic circular dichroism. Samples with Mo spacers of two different thicknesses (0.9 nm and 1.8 nm) were investigated. Mo atoms receive a magnetic moment of ?0.21μ_B in the alloy. In the multilayer with the thinner Mo spacer (d_Mo = 0.9 nm) the magnetic moment is much smaller (?0.03μ_B). In both cases the measured induced moment at the Mo site is oriented antiparallel to the moment at the Co atoms. The presence of the induced moment in the Mo spacer coincides with antiferromagnetic coupling between the Co component slabs. In contrast, neither measurable induced moment at the Mo site nor interlayer coupling between the Co layers has been found for the multilayer with the thicker Mo spacer. Possible mechanisms of the coupling associated with the induced moment are discussed in detail.     

Vacuum ultraviolet generation in phase matched carbon monoxide

Resonantly enhanced four-wave sum frequency mixing in phase matched carbon monoxide leads to the generation of continuously tunable over 1200 cm^-1 coherent VUV radiation in the 1150 Å range. Experiments allow to determine the VUV absorption cross sections and indices of refraction of CO. Multiphoton photolysis of CO has been observed and confirmed by the VUV absorption in atomic carbon.     

Bosons doubling

It is shown that next-nearest-neighbor interactions may lead to unusual paramagnetic or ferromagnetic phases which physical content is radically different from the standard phases. Actually there are several particles described by the same quantum field in a manner similar to the species doubling of the lattice fermions. The renormalizability of the theory is proven at the one loop level. Received: 26 June 2000 / Published online: 31 August 2000     

A phase unwrapping technique for object relief determination

Phase shifting methods are widely used in photomechanics to analyse fringe patterns obtained from interferometry, moiré, etc. The phase is determined by modulo 2π and an unwrapping process is needed. An algorithm is presented which avoids most of the inconsistency of the phase field. It can be applied to the relief determination of virtually any object shape. In this paper, two applications are performed using the projection of a parallel line grating with a pitch equal to 4 mm. The accuracy is shown to be around 0…1 mm.     

A constitutive model for semi-crystalline polymer deformation involving lamellar fragmentation

The mechanism of lamellar fragmentation in the semi-crystalline polymers with spherulitic structure, is observed at the beginning of plastic flow. It causes significant damage. This elementary mechanism is considered here as a result of plastic deformation coupled with damage, in the framework of generalized standard materials. The simplicity and the efficiency of the proposed approach come from the fact that the semi-crystalline polymers are considered as a macromolecular network bridled by intra-lamellar cohesive forces. Tensile tests and relaxation tests demonstrate the usefulness of a damage–plasticity coupled model.     

A magnetic and Mössbauer study of magnetic ordering and vacancy clustering in Cu5FeS4

Magnetic susceptibilities and Mössbauer spectra recorded at temperatures between 4° and 300°K show that the low temperature form of Cu₅FeS₄, bornite, orders magnetically at 76±2°K. At a lower temperature 8°K a second magnetic phase transition occurs. The Mössbauer spectra suggest that there is significant partial disordering of cations and vacancies in tetrahedral holes of the face-centred cubic sulphur lattice. Thermoelectric power measurements indicate that bornite is a p-type semiconductor.For a three dimensional magnetic superexchange interaction between Fe(III) atoms a small super-transferred spin density would be required on intermediate Cu(I) atoms.     

Reproducibility of low and high concentration data in reversed-phase liquid chromatography. II. Overloaded band profiles on Chromolith-C18

Single-component adsorption isotherm data were acquired by frontal analysis (FA) for six low molecular weight compounds (phenol, aniline, caffeine, o-toluidine, p-toluidine and propylbenzoate) on one Chromolith-C18 column (#30, Merck, Darmstadt, Germany), using different methanol:water solutions (composition between 60/40 and 15/85 v/v, depending on the solute) as the mobile phase. These data were modeled for best agreement between the experimental data points and the adsorption isotherm model. The adsorption-energy distributions were also derived and used for the selection of the best isotherm model. Widely different models were obtained for these six compounds, four being convex upward (i.e., Langmuirian) and two having at least one inflection point. Overloaded band profiles corresponding to two different sample sizes (a low and a high loading factor) were recorded on six monolithic columns (#30-35) belonging to the same manufactured lot. These experimental band profiles were compared to the profiles calculated from the isotherm measured by FA on the first column, using the equilibrium-dispersive (ED) model of chromatography. For four of the six columns (#30, #32, #33, and #35), the reproducibility was better than 5 and 2.5% for the low and the high concentration profiles, respectively. On the other two columns (#31 and #34), the bands showed significant and systematic retention time shifts for all six compounds (with nearly identical band shapes), the relative adsorption being between 6 and 15% stronger on column #31 or between 2 and 7% lower on column #34. These differences seem to be correlated with the differences in the total porosities of these columns, which differ by 3% from columns #31 to #34, the higher porosity column giving the stronger adsorption.     

The preparation of a stable 2-pyridylboronate and its reactivity in the Suzuki-Miyaura cross-coupling reaction

The preparation and reactivity of a 2-pyridylboronate stabilised by N-phenyldiethanolamine is described. In Suzuki-Miyaura cross-coupling reactions employing this boronate, significant aryl-aryl exchange from the phosphine ligand was observed with some combinations of ligand and substrates. The amount of the exchange by-product can be minimised by appropriate choice of phosphine ligand.