Firing-Induced Microstructural Properties of Quasi-Diamagnetic Carbonate-Based Porous Ceramics: a <Superscript>1</Superscript>H NMR Relaxation Correlation Study

This study deals with the application of two-dimensional proton nuclear magnetic resonance relaxometry (2D ¹H NMR-R) to the characterization of porous ceramics nearly free of magnetic compounds. Different microstructural properties were obtained by firing a diamagnetic mixture of kaolin, calcium, and magnesium carbonate over a wide range of maximum temperatures (600–1100 °C) and firing times at the maximum temperature (soaking times) (0–10 h). The 2D ¹H NMR-R method relies on the correlated measurement of ¹H longitudinal (T ₁) and transverse (T ₂) relaxation times of pore-filling water by which the properties of the interconnected pore space may be investigated. In the absence of significant magnetic susceptibility effect due to para- and ferro-magnetic compounds, the 2D ¹H NMR-R maps allow studying the conjoint effects on pore size distribution and inter-pore coupling due to the variations in both time and temperature of firing. The NMR experiments were performed with a low-field ¹H NMR sensor, which allows non-destructive and in situ analysis. For ceramic specimens fired at 600 and 700 °C, the fraction of smallest pores increases with firing time at the expenses of those with intermediate size. The pore shrinkage occurring at this stage, and likely associated with the transformation of kaolinite in metakaolinite, is affected in a similar way by soaking time and firing temperature, in line with the concept of equivalent firing temperature. At temperatures from 800 to 1100 °C, the structural modifications involving interconnectivity and average pore size are driven primarily by firing temperature and, secondarily, by soaking time. The 2D ¹H NMR-R results are confirmed by more traditional, but destructive, mineralogical, and structural analyses like X-ray powder diffraction, helium pycnometry, mercury intrusion porosimetry, and nitrogen adsorption/desorption method.     

Covariant Sectors with Infinite Dimension¶and Positivity of the Energy

Let ? be a local conformal net of von Neumann algebras on S ¹ and ρ a M?bius covariant representation of ?, possibly with infinite dimension. If ρ has finite index, ρ has automatically positive energy. If ρ has infinite index, we show the spectrum of the energy always to contain the positive real line, but, as seen by an example, it may contain negative values. We then consider nets with Haag duality on ℝ, or equivalently sectors with non-solitonic extension to the dual net; we give a criterion for irreducible sectors to have positive energy, namely this is the case iff there exists an unbounded M?bius covariant left inverse. As a consequence the class of sectors with positive energy is stable under composition, conjugation and direct integral decomposition. Received: 21 April 1997 / Accepted: 23 September 1997     

Beyond the standard model: Working group report

This report summarises the activities of the working group on ‘Physics beyond the Standard Model’. The results of investigations in incorporatingR-parity in grand unification, the possibility of a light charged Higgs boson in extension of MSSM and radiative generation of neutral vector boson self-couplings within the MSSM are described. Also given is an account of activities in neutrino physics, namely a proposal for a study of the atmospheric muon anomaly in deep underground mines, a field theoretic study of neutrino oscillations and a mechanism to generate appropriate masses of three active plus one sterile neutrino species.     

A complete treatment of a steady-state four-level model for the interpretation of OH laser-induced fluorescence measurements in atmospheric pressure flames

In order to obtain OH concentration measurements in atmospheric pressure flames from saturated fluorescence signal, we have developed a stationary four-level model. A general relationship between the measured upper state population and the total number density has been derived. The effects of the imbalance between the rotational transfer rates in the upper and ground states is analyzed. We show that in the case of comparable rotational rates, the results of our treatment are similar to the ones obtained with the balanced cross rate model. A set of complementary data which should facilitate absolute OH concentration measurements is also pointed out.     

A heterodyne interferometric polarimeter for the detection of jones and stokes polarization vectors

A heterodyne interferometric polarimeter for detection of the Jones components and Stokes parameters is demonstrated. The measurement of both sets of quantities for various polarization states is achieved with excellent precision. The details of the corresponding Lissajous picture (ellipse) can be visualized in real time. Finally, the polarization data collected at the output of a highly birefringent fiber have been used for submillimetric beat-Length measurements.     

Lateral IBIC characterization of single crystal synthetic diamond detectors

In order to evaluate the charge collection efficiency (CCE) profile of single‐crystal diamond devices based on a p‐type/intrinsic/metal configuration, a lateral Ion Beam Induced Charge (IBIC) analysis was performed over their cleaved cross sections using a 2 MeV proton microbeam. CCE profiles in the depth direction were extracted from the cross‐sectional maps at variable bias voltage. IBIC spectra relevant to the depletion region extending beneath the frontal Schottky electrode show a 100% CCE, with a spectral resolution of about 1.5%. The dependence of the width of the high efficiency region from applied bias voltage allows the constant residual doping concentration of the active region to be evaluated. The region where the electric field is absent shows an exponentially decreasing CCE profile, from which it is possible to estimate the diffusion length of the minority carriers by means of a drift–diffusion model. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Thermal expansion of supported and freestanding graphene: lattice constant versus interatomic distance

By using ab initio molecular dynamics calculations, we show that even where the graphene lattice constant contracts, as previously reported for freestanding graphene below room temperature, the average carbon-carbon distance increases with temperature, in both free and supported graphene. This results in a larger corrugation at higher temperature, which can affect the interaction between graphene and the supporting substrate. For a weakly interacting system as graphene/Ir(111), we confirm the results using an experimental approach which gives direct access to interatomic distances.     

Entanglement cost in practical scenarios

We quantify the one-shot entanglement cost of an arbitrary bipartite state, that is, the minimum number of singlets needed by two distant parties to create a single copy of the state up to a finite accuracy, by using local operations and classical communication only. This analysis, in contrast to the traditional one, pertains to scenarios of practical relevance, in which resources are finite and transformations can be achieved only approximately. Moreover, it unveils a fundamental relation between two well-known entanglement measures, namely, the Schmidt number and the entanglement of formation. Using this relation, we are able to recover the usual expression of the entanglement cost as a special case.