Hybrid Superconducting Neutron Detectors

A new neutron detection concept is presented that is based on superconductive niobium (Nb) strips coated by a boron (B) layer. The working principle of the detector relies on the nuclear reaction 10B+n $\rightarrow$ $\alpha$+ 7Li , with $\alpha$ and Li ions generating a hot spot on the current-biased Nb strip which in turn induces a superconducting-normal state transition. The latter is recognized as a voltage signal which is the evidence of the incident neutron. The above described detection principle has been experimentally assessed and verified by irradiating the samples with a pulsed neutron beam at the ISIS spallation neutron source (UK). It is found that the boron coated superconducting strips, kept at a temperature T = 8 K and current-biased below the critical current Ic, are driven into the normal state upon thermal neutron irradiation. As a result of the transition, voltage pulses in excess of 40 mV are measured while the bias current can be properly modulated to bring the strip back to the superconducting state, thus resetting the detector. Measurements on the counting rate of the device are presented and the future perspectives leading to neutron detectors with unprecedented spatial resolutions and efficiency are highlighted.Comment: 8 pages 6 figure

Sorption of CO2, CH4 and Their Mixtures in Amorphous Poly(2,6-dimethyl-1,4-phenylene)oxide (PPO)

Sorption of pure CO2 and CH4 and CO2/CH4 binary gas mixtures in amorphous glassy Poly(2,6-dimethyl-1,4-phenylene) oxide (PPO) at 35 °C up to 1000 Torr was investigated. Sorption experiments were carried out using an approach that combines barometry with FTIR spectroscopy in the transmission mode to quantify the sorption of pure and mixed gases in polymers. The pressure range was chosen to prevent any variation of the glassy polymer density. The solubility within the polymer of the CO2 present in the gaseous binary mixtures was practically coincident with the solubility of pure gaseous CO2, up to a total pressure of the gaseous mixtures equal to 1000 Torr and for CO2 mole fractions of ~0.5 mol mol-1 and ~0.3 mol mol-1. The Non-Equilibrium Thermodynamics for Glassy Polymers (NET-GP) modelling approach has been applied to the Non-Random Hydrogen Bonding (NRHB) lattice fluid model to fit the solubility data of pure gases. We have assumed here that no specific interactions were occurring between the matrix and the absorbed gas. The same thermodynamic approach has been then used to predict the solubility of CO2/CH4 mixed gases in PPO, resulting in a deviation lower than 9.5% from the experimental results for CO2 solubility

Survey on Adsorption of Low Molecular Weight Compounds in Cu-BTC Metal–Organic Framework: Experimental Results and Thermodynamic Modeling

This contribution aims at providing a critical overview of experimental results for the sorption of low molecular weight compounds in the Cu-BTC Metal–Organic Framework (MOF) and of their interpretation using available and new, specifically developed, theoretical approaches. First, a literature review of experimental results for the sorption of gases and vapors is presented, with particular focus on the results obtained from vibrational spectroscopy techniques. Then, an overview of theoretical models available in the literature is presented starting from semiempirical theoretical approaches suitable to interpret the adsorption thermodynamics of gases and vapors in Cu-BTC. A more detailed description is provided of a recently proposed Lattice Fluid approach, the Rigid Adsorbent Lattice Fluid (RALF) model. In addition, to deal with the cases where specific self- and cross-interactions (e.g., H-bonding, Lewis acid/Lewis base interactions) play a role, a modification of the RALF model, i.e., the RALFHB model, is introduced here for the first time. An extension of both RALF and RALFHB is also presented to cope with the cases in which the heterogeneity of the rigid adsorbent displaying a different kind of adsorbent cages is of relevance, as it occurs for the adsorption of some low molecular weight substances in Cu-BTC MOF

High-efficiency mixing of fine powders via sound assisted fluidized bed for metal foam production by an innovative cold gas dynamic spray deposition method

Metal foams are an interesting class of materials with very low specific weight and unusual physical, mechanical and acoustic properties due to the porous structure (1). These materials are currently manufactured by means of several conventional processes (2), limited by the impossibility to produce foams with complex geometry. This paper deals with the study of an innovative method to produce complex shaped precursors for aluminum foams through cold gas dynamic spray deposition process (CGDS), aluminum alloy (AlSi12) and titanium-hydride (TiH2) being the metal and the blowing agent, respectively. However, the success of this approach strongly depends on the achievement of a homogenous and deep mixing between AlSi12 and TiH2 fine powders, belonging to group C of Geldart’s classification. Classical mixing methods (such as tumbling mixers, convective mixers, high-shear mixers, etc.) are suitable for large non-cohesive particles (\u3e 30µm) but not for micronic particles (3), agglomerated due to strong interparticle forces. Alternatively, new wet and dry mixing techniques have been proposed for fine particles (4), suffering from different disadvantages: additional steps of filtration/drying are needed for wet methods, whereas, dry methods generally involves the reduction of the granulometry and the damaging or contamination of the original powders. The sound assisted fluidization technology (140dB-80Hz) has been adopted in this work to overcome the technical issues of mixing cohesive powders (5), thus obtaining a mixing to the scale of the primary particles in a simple, economic, not intrusive and not destructive way (the properties and morphology of the original particles were preserved). Therefore, the mixed powders were then sprayed by means of the proposed CGDS process on a stainless steel sheet to obtain the precursor. This was then heated up in a furnace at 600°C for 10 minutes to obtain the foam. In particular, two different types of mixtures with 1 wt% and 2.5 wt% of TiH2 were investigated; moreover, air compressed as well as helium were used as CGDS carrier gas in order to ensure a higher impact velocity and a better compacting of the powders. A very efficient mixing of powders has been achieved as confirmed by SEM/EDS analysis performed on samples taken from the sound assisted fluidized bed (Fig.1a) and by the time-dependence of the mixing degree (Fig.1b). Macrographs of created porous structures (Fig.2) showed that the coupling of sound assisted fluidization and CGDS process under optimal conditions is a promising and effective technique in manufacturing aluminum precursors for metal foams. Please click Additional Files below to see the full abstract

A Hyphenated Approach Combining Pressure-Decay and in Situ FT-NIR Spectroscopy to Monitor Penetrant Sorption and Concurrent Swelling in Polymers

A new hyphenated technique based on simultaneous in situ FT-NIR spectroscopy and pressure-decay measurements has been implemented to study sorption of low-molecular-weight compounds in polymeric membranes and the induced swelling of the matrix. The FT-NIR measurements are performed in the transmission mode and, besides sorption equilibrium and kinetics, allow also the straightforward measurement of polymer swelling. The pressure decay method is used to provide quantitative information on the concentration of penetrant sorbed in the polymer. This measurement, once combined with the photometric data, allows an accurate estimation of the molar absorptivity of the analytical peaks as well. To validate the new experimental approach, sorption of CO2 in polydimethylsiloxane at 35 °C and at pressures up to 9 bar has been investigated and the results are compared with available literature data

Excitation energy and deformation of the 1/2+[431] intruder band in 107Tc^{107}Tc

The already detailed study of $^{107}Tc$ nucleus was complemented by a search for microsecond isomers at very low energy. For this purpose, this neutron-rich nucleus was produced by thermal-neutron-induced fission of $^{241}Pu$. We have found a new 30.1 keV microsecond isomeric state which deexcites to the ground state by a strongly-hindered E1 transition. This isomer was identified as the 3/2+ level of the 1/2+[431] intruder band in $^{107}Tc$ and is also the lowest-lying member of the band. The very low energy of the band head suggests a large quadrupole deformation. From a comparison with $^{105}Tc$,where more information is known about the intruder band, it is deduced that the 1/2+[431] band has a quadrupole deformation, $\epsilon_{2} \geq$ 0.35 and a possible triaxial shape, $\gamma \approx$ 20°

Recent measurements of the spherical and deformed isomers using the Lohengrin fission-fragment spectrometer

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