Magneto-Structural analysis of rotating electrical machines

The vibrations of the stator core of a rotating electrical machine induce acoustic noise. These oscillations of the stator yoke are excited of the force density due to the magnetic field in the air gap. This requires a transient magnetic field analysis coupled with a dynamic mechanical analysis. Coupling these two different physical fields results in a high numerical effort and usually one direction of the interaction is disregarded. This paper presents a method to calculate the vibrations of a stator core under design operating conditions. For this purpose, harmonic electromagnetic excitation forces have been calculated in a linear magnetic field analyses using the finite element method. The resulting forces have been applied to a linear structural dynamic FE model in the frequency domain. The results of the calculations are harmonic velocities specified by amplitude and phase from the structural surface of the stator core. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Modelling thermoplastic material behaviour of dual-phase steels on a microscopic length scale - numerical treatment

On a microscopic length scale dual-phase steels exhibit a polycrystalline microstructure consisting of ferrite and martensite. In this work it is assumed that the martensitic phase behaves purely thermoelastic while for the ferritic phase a thermoplastic material model was developed based on the assumption that the driving mechanism for persistent deformation is the movement of dislocations on preferred planes in preferred directions. The necessary shear stress to move dislocations at a certain temperature and deformation rate is assumed to possess contributions from the atomic lattice, alloying atoms and the dislocation structure. To consider the influence of the dislocation structure, dislocation densities are introduced as state variables for which temperature and deformation rate dependent evolution equations are formulated. Since for general loading histories the model equations cannot be integrated analytically, a time discretized form of the model equations with an appropriate solution algorithm is presented. (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

On the dimers of β-tocopherol

Upon oxidation in aprotic media, β-tocopherol (2) forms a spiro-dimer (10) as the main product. The reaction mechanism is a hetero-Diels-Alder process with inverse electron demand of two intermediate ortho-quinone methide molecules. The spiro-dimer can be reduced to the corresponding symmetric ethano-dimer (11). In contrast to the well-studied α-tocopherol case, spiro-dimer and ethano-dimer do not form a reversible redox pair, their interconversion is accompanied by coupling reactions at C-7 with 7a-(β-tocopher-5a-yl)-β-tocopherol (13) as the main byproduct besides some oligomeric material. The full NMR assignments (¹H, ¹³C) of the β-tocopherol oxidation products are given.     

Colloidal stability of aqueous nanofibrillated cellulose dispersions

Cellulose nanofibrils constitute an attractive raw material for carbon-neutral, biodegradable, nanostructured materials. Aqueous suspensions of these nanofibrils are stabilized by electrostatic repulsion arising from deprotonated carboxyl groups at the fibril surface. In the present work, a new model is developed for predicting colloidal stability by considering deprotonation and electrostatic screening. This model predicts the fibril-fibril interaction potential at a given pH in a given ionic strength environment. Experiments support the model predictions that aggregation is induced by decreasing the pH, thus reducing the surface charge, or by increasing the salt concentration. It is shown that the primary mechanism for aggregation upon the addition of salt is the surface charge reduction through specific interactions of counterions with the deprotonated carboxyl groups, and the screening effect of the salt is of secondary importance.     

Effect of pH on the synthesis and properties of luminescent SiO2/calcium phosphate:Eu3+ core-shell nanoparticles

A novel method for the synthesis of luminescent SiO(2)/calcium phosphate (CaP):Eu(3+) core-shell nanoparticles (NPs) was developed via a sol-gel route followed by annealing at a temperature of 800 °C. The object of this study was the investigation of the effect of pH on the formation of a CaP shell around the silica core. The resulting annealed NPs exhibited an amorphous SiO(2) core and a crystalline luminescent shell. The formation of a CaP layer was possible at pH below 4.5 and above 6.5 during the coating step. The crystal structure of the shell was studied by X-ray diffraction analysis. Hydroxyapatite (HAp) and α-tricalcium phosphate were detected as crystal phases of the surrounding layer. However, NPs produced under basic conditions exhibited a higher crystallinity of the CaP layer than did samples coated at pH below 4.5. In the pH interval between 4.5 and 6.5, no shell growth but the formation of secondary NPs containing CaO and Ca(OH)(2) was observed. Furthermore, SiO(2)/CP:Eu(3+) core-shell NPs were investigated by transmission electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy, inductively coupled plasma optical emission spectrometry, and photoluminescence spectroscopy. The resulting HAp-coated NPs were successfully tested by a cell-culture-based viability assay with respect to a later application as a luminescent marker for biomedical applications.     

Characterizing the molecular order of phosphonic acid self-assembled monolayers on indium tin oxide surfaces

Self-assembled monolayers (SAMs) of alkanephosphonic acids with chain lengths between 8 and 18 carbon units were formed on thin films of indium tin oxide (ITO) sputter-deposited on silicon substrates with 400 nm thermally grown SiO(2). The silicon substrates, while not intended for use in near-IR or visible optics applications, do provide smooth surfaces that permit systematic engineering of grain size and surface roughness as a function of the sputter pressure. Argon sputter pressures from 4 to 20 mTorr show systematic changes in surface morphology ranging from smooth, micrometer-sized grain structures to <50 nm grains with 3× higher surface roughness. Near-edge X-ray absorption fine structure (NEXAFS) spectroscopy experiments are conducted for alkanephosphonic acids deposited on these wide range of ITO surfaces to evaluate the effects of these morphological features on monolayer ordering. Results indicate that long-chain SAMs are more highly ordered, and have a smaller tilt angle, than short-chain SAMs. Surprisingly, the 1-octadecyl phosphonic acids maintain their order as the lateral grain dimensions of the ITO surface shrink to ～50 nm. It is only when the ITO surface roughness becomes greater than the SAM chain length (～15 ?) that SAMs are observed to become relatively disordered.     

Supramolecular functionalization of electron-beam generated nanostructures

Electron-beam lithography was used to pattern poly(styrene-co-(methyldiaminotriazine) styrene) (PS-Triaz). These polymer nanopatterns were utilized as molecular scaffolds for assembling complementary thymine-functionalized CdSe-ZnS quantum dots (Thy-QDs) via three-point hydrogen-bonding molecular recognition. This interaction was very specific, with N-methyl thymine-functionalized QDs (MeThy-QDs) not depositing on the surfaces. The "lock and key" specificity of the assembly is mirrored in the disassembly process, where complete removal of the QD was observed using a competing thymine guest.     

Large inclusion constants of ��-cyclodextrin with carborane derivatives

Complexation of some o-, m- and p-carborane derivatives with ??-cyclodextrin was investigated using phenolphthalein in pH 10.5 (0.05 mol dm^?3) borate buffer. Some carborane derivatives indicated large inclusion constants K_ass > 1 × 10⁵ dm³ mol^?1.