Atom formation and dissipation in electrothermal atomization

For a number of metals the mechanisms of atom formation and dissipation have been studied using a carbon mini-tube furnace and a carbon-strip heater. As to the atom formation rate two groups of metals can be distinguished: a group in which the sublimation of the metal, generated by the carbon reduction of the oxide, is rate determining and a group in which the carbon reduction of the metal oxide itself is the rate-determining process. Exceptionally the aluminium atomization is governed by the gas phase dissociation of the aluminium—oxide bond. There also seems to be two distinctly different dissipation mechanisms: one purely gas phase diffusional and the other a short-range evaporation—condensation type. Material loss by diffusion through the furnace wall is negligible compared with these dissipation mechanisms. However, the atom supply is strongly influenced by the porosity of the carbon wall.     

Characterization of the crystallization behavior of the eutectic-forming binary system polyoxyethylene and glutaric acid. I. melting and crystallization behavior

The crystallization characteristics of the binary system polyoxyethylene (PEO)-glutaric acid were determined. From the extrapolated melting point depression data the heat of fusion for PEO is 2506 ± 200 cal/mole of repeat unit while the heat of solution for the glutaric acid amounts to 6.7 ± 1.2 cal/cm³. A melting point of 348 K is found for the high-molecular-weight PEO. A calorimetric glass-transition temperature for mixtures of the two components is relatively independent of the melt composition and appears at 217 K. A eutectic is observed whose composition and melting temperature depend on the nature of the PEO crystal phase.     

Kinetics of reversible recombination of aromatic C-centered radicals

The kinetics of the reversible recombination of the 2-phenyl- (I), 2-p-methoxyphenyl-(II), and 2-p-nitrophenyl-3-oxo-2,3-dihydrobenzothiophene-2-yl (III) radicals have been investigated. Recombination rate constants of R(I–III) have been determined in different solvents (2k₁ ～ 10⁹ M^?1 s^?1). The rate of reaction (I) with R(I–III) decreases with increasing solvent viscosity η. In the toluene-vaseline oil mixture (2 ? η ? 120 cP) the recombination of R(I–III) is molecular mobility limited. The thermodynamic parameters of reaction (I) have been determined: ΔH⁰ = 20–30 kcal/mol. Activation volumes ΔV for recombination of R(II) have been measured. In n-propanol ΔV is equal to the viscous flow activation volume of the solvent ΔV. In toluene and chloroform ΔV < ΔV. For the last two solvents the activation volumes of the cage reaction have been estimated ΔV = ?(2–3) cm³/mol. Visible-range absorption spectra and ESR spectra have been recorded for R(I–III). The role of cage effect in the reactivity anisotropy averaging of R(I–III) is discussed. The potential of the high-pressure tests for deriving information about the elementary act of a fast bimolecular reaction is considered.     

Deformation and Flow Driven by Osmotic Processes in Porous Materials: Application to Bituminised Waste Materials

This paper presents a coupled Chemo-Hydro-Mechanical (CHM) analysis of the behaviour of leached Bituminized Waste materials (BW). Under geological disposal conditions the main factor that affects the long-term behaviour of this kind of materials is water uptake. First, the long-term behavior of BW in contact with water has been studied. A formulation has been proposed for the analysis of deformation induced by dissolution of salts in porous media in contact with water. The equations include the effect of coupled transport phenomena and the formulation has been included as an extension in the coupled THM program CODE_BRIGHT. The impact of osmotic forces on the swelling of the material has been investigated by simulating water uptake swelling tests under confined conditions. The numerical analysis has proven to be able to furnish a satisfactory representation of the main observed patterns of the behaviour. A sensitivity analysis has also been carried out to examine the effect of various key parameters.     

PLQP & Company: Decidable Logics for Quantum Algorithms

We introduce a probabilistic modal (dynamic-epistemic) quantum logic PLQP for reasoning about quantum algorithms. We illustrate its expressivity by using it to encode the correctness of the well-known quantum search algorithm, as well as of a quantum protocol known to solve one of the paradigmatic tasks from classical distributed computing (the leader election problem). We also provide a general method (extending an idea employed in the decidability proof in Dunn et al. (J. Symb. Log. 70:353–359, 2005)) for proving the decidability of a range of quantum logics, interpreted on finite-dimensional Hilbert spaces. We give general conditions for the applicability of this method, and in particular we apply it to prove the decidability of PLQP.     

The logic of justified belief,explicit knowledge,and conclusive evidence

We present a complete, decidable logic for reasoning about a notion of completely trustworthy (“conclusive”) evidence and its relations to justifiable (implicit) belief and knowledge, as well as to their explicit justifications. This logic makes use of a number of evidence-related notions such as availability, admissibility, and “goodness” of a piece of evidence, and is based on an innovative modification of the Fitting semantics for Artemov?s Justification Logic designed to preempt Gettier-type counterexamples. We combine this with ideas from belief revision and awareness logics to provide an account for explicitly justified (defeasible) knowledge based on conclusive evidence that addresses the problem of (logical) omniscience.     

Surface transfer doping of hydrogen-terminated diamond by C60F48: energy level scheme and doping efficiency

Surface sensitive C1s core level photoelectron spectroscopy was used to examine the electronic properties of C(60)F(48) molecules on the C(100):H surface. An upward band bending of 0.74 eV in response to surface transfer doping by fluorofullerene molecules is measured. Two distinct molecular charge states of C(60)F(48) are identified and their relative concentration determined as a function of coverage. One corresponds to ionized molecules that participate in surface charge transfer and the other to neutral molecules that do not. The position of the lowest unoccupied molecular orbital of neutral C(60)F(48) which is the relevant acceptor level for transfer doping lies initially 0.6 eV below the valence band maximum and shifts upwards in the course of transfer doping by up to 0.43 eV due to a doping induced surface dipole. This upward shift in conjunction with the band bending determines the occupation of the acceptor level and limits the ultimately achievable hole concentration with C(60)F(48) as a surface acceptor to values close to 10(13) cm(-2) as reported in the literature.     

The nanostructural analysis of hydrogenated silicon films based on positron annihilation studies

Due to the complex nature of hydrogenated amorphous and microcrystalline silicon (a-Si:H; μc-Si:H) a profound understanding of the Si:H nanostructure and its relation to the Staebler–Wronski effect (SWE) is still lacking. In order to gain more insight into the nanostructure we present a detailed study on a set of Si:H samples with a wide variety of nanostructural properties, including dense up to porous films and amorphous up to highly crystalline films, using Doppler broadening positron annihilation spectroscopy (DB-PAS) and Fourier Transform infrared (FTIR) spectroscopy. The results obtained from these material characterisation techniques show that they are powerful complementary methods in the analysis of the Si:H nanostructure. Both techniques indicate that the dominant type of open volume deficiency in device grade a-Si:H seems to be the divacancy, which is in line with earlier positron annihilation lifetime spectroscopy (PALS), Doppler broadening (DB) PAS and FTIR studies.