Heat Transfer Study in a Discoidal System: The Influence of an Impinging Jet and Rotation

Abstract

This article presents an experimental study of the local heat transfer on the rotor surface in a discoidal rotor-stator system air-gap in which an air jet comes through the stator and impinges the rotor. To determine the surface temperatures, measurements were taken on the rotor, using an experimental technique based on infrared thermography. A thermal balance was used to identify the local convective heat transfer coefficient. The influence of the axial Reynolds number Re _j and the rotational Reynolds number Re was measured and compared with the data available in the literature. Local convective heat transfer coefficients were obtained for a dimensionless space between the two disks G = 0.01, for Re _j between 0 and 41,666, and for Re between 20,000 and 516,000. The flow data found in the literature can be used to explain the heat transfers in this small space configuration. In fact, the rotating disk can be divided into two influence zones: one dominated by the air jet near the center of the rotor and one affected by both the air jet and rotation. Heat transfers with non zero impinging jets appear to be continuously improved compared to those with no jets, even if the two influence zones mentioned previously are situated differently.     

Hole Migration in Telomere-Based Oligonucleotide Anions and G-Quadruplexes

Vacuum ultraviolet photoionization of a gas-phase oligonucleotide anion leads to the formation of a valence hole. This hole migrates towards an energetically favorable site where it can weaken bonds and ultimately lead to bond cleavage. We have studied Vacuum UV photoionization of deprotonated oligonucleotides containing the human telomere sequence dTTAGGG and G-quadruplex structures consisting of four dTGGGGT single strands, stabilized by NH₄⁺ counter ions. The oligonucleotide and G-quadruplex anions were confined in a radiofrequency ion trap, interfaced with a synchrotron beamline and the photofragmentation was studied using time-of-flight mass spectrometry. Oligonucleotide 12-mers containing the 5'-TTAGGG sequence were found to predominantly break in the GGG region, whereas no selective bond cleavage region was observed for the reversed 5'-GGGATT sequence. For G-quadruplex structures, fragmentation was quenched and mostly non-dissociative single and double electron removal was observed.     

Unusual sum rule for Clebsch–Gordan coefficients

Letters in Mathematical Physics - We present a new sum rule for Clebsch–Gordan coefficients using generalized characters of irreducible representations of the rotation group. The identity is...     

Second-harmonic generation in a doubly resonant semiconductor microcavity

We demonstrate second-harmonic generation in a doubly resonant semiconductor microcavity. The monolithic cavity consists of an AlGaAs active medium sandwiched between two AlGaAs/AlAs dual-wavelength mirrors. The mirrors do not have any apparent periodicity because, unlike single- or dual-wavelength Bragg reflectors, they are engineered with dispersion taken into account. Quasi-phase matching is obtained by addition of the appropriate phases at reflection so as to compensate for the dephasing between the fundamental and the second-harmonic fields.     

Thermodynamic analysis of GaAs growth by molecular beam epitaxy at the surface structure transition from 3 × 1 to 4 × 2

The molecular beam epitaxy (MBE) growth of GaAs layers on a single crystal is studied in relation with the stability domain of the GaAs compound in the Ga-As binary system. The growth parameters, i.e. The Ga and As impinging atomic flows, are compared to the necessary flows as calculated by thermodynamics. In order to take into account in the real growth situation, which is not strictly at equilibrium, the flow balance at the surface of the crystal between the impinging flows and the growth and evaporated flows is written for quasi-equilibrium growth conditions, including condensation and evaporation coefficients that split the “so-called” sticking coefficient in parts related to the condensation or the evaporation phenomenon for each gaseous species. A comparison between the quasi-equilibrium simulation of the growth and the experiment is made with the assumption that the surface structure transition from gallium-stabilized to arsenic-stabilized surface corresponds to the growth of a GaAs crystal at its solidus boundary rich in gallium. The surface structure transitions are observed by reflection high energy electron diffraction (RHEED) and the impinging atomic flows are carefully calibrated and also controlled by RHEED oscillations as observed after gallium or arsenic excess as deposited on the surface. The results show that the growth is effectively performed close to equilibrium conditions as evidenced by the values of the condensations and evaporation coefficients. The evaporation coefficient of gallium is 0.4, showing that this component is the supersaturated one at the surface, and this value agrees with theoretical predictions for an evaporation process (during growth) controlled by the surface diffusion process of monoatomic species between steps.     

Formation of negative oxidation states of platinum and gold in redox ionic liquid: Electrochemical evidence

The electrochemical reduction of noble metal electrodes in the presence of redox ionic liquid, 1-ferrocenylethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, [FcEMIM][TFSI], was investigated by cyclic voltammetry. Our experiments suggest the formation of metal with negative oxidation states, in the cases of platinum and gold electrodes [M_n⁻, FcEMIM⁺]. By analogy with the previous work, the formation of these phases is concomitant with the insertion of the supporting electrolyte; which correspond in our experimental condition to the redox cation of the ionic liquid. As an exciting result, the electrochemical investigations of the reduced electrode in electrolytic solution, containing solvent and supporting electrolyte, evidence the presence of the ferrocene groups at the electrode surface. Moreover, the reduced electrode exhibits the presence of the ferrocene even after, contact with air, after ultrasound, and after physical polishing, highlighting the large stability of this organo-metallic phases formed in this media. The AFM investigations demonstrate the morphological change of the platinum surface after the reduction process. Finally, our works bring a formal electrochemical proof of the presence of the ionic liquid cation inside the electrode material after the cathodic treatment in this media.     

NMR and X-ray diffraction analysis of 3-thioamido-5-phosphono-1-cyclohexene derivatives: Conformational and stereochemical assignments

Reaction of N-(dienyl)-4-(R)-phenyloxazolidin-2-thione (1) with 1-diethoxyphosphoryl-1-buten-3-one (2a), methyl 3-(diethoxyphosphoryl)acrylate (2b) and 3-(diethoxyphosphoryl)acrylonitrile (2c) furnished the [4 + 2] cycloadducts 3a, 3b and 3c, respectively, as single stereoisomers, confirming the efficiency of the oxazolidin-2-thione chiral auxiliary in the facial discrimination of Diels–Alder reactions. The absolute configuration of the 3,4,5-trisubstituted cyclohexene derivatives (3a–c) was established by X-ray diffraction analysis. NMR studies confirmed the relative stereochemistries and showed two possible conformers in solution.     

Transferable specific scaling factors for interpretation of infrared spectra of biomolecules from density functional theory

A set of transferable local scaling factors is established for assignment of infrared spectra of molecular systems of biological interest experimentally recorded under gas-phase conditions. Each scaling factor is specific for an experimentally observable vibrational mode chosen among those bringing significant structural information. Those factors are provided for harmonic calculations at the DFT B3LYP and DFT B3PW91 levels respectively with 7 and 2 different basis sets. The used training set of neutral molecules comprises nucleobases, aminoacids, peptides, sugars, and neurotransmitters. The proposed specific scaling factors usable for unambiguous conformer assignments lead to typical prediction errors ca. 10 cm(-1) for free and moderately hydrogen-bonded group frequencies with red-shifts up to 200 cm(-1).     

Controlled assembly of bacteria on chemical patterns using soft lithography

Highly ordered arrays of single living bacteria were obtained by selective adsorption of bacteria onto chemical patterns with micrometric resolution. The chemically engineered template surfaces were prepared with the combination of microcontact printing process and a simple incubation technique. This methodology can be used for fundamental studies of bacterium's inner mechanisms and sub-cellular organization as well as for interfacing living bacteria with artificial microsystems.