Tunnelling spectra of individual magnetic endofullerene molecules

The manipulation of single magnetic molecules may enable new strategies for high-density information storage and quantum-state control. However, progress in these areas depends on developing techniques for addressing individual molecules and controlling their spin. Here, we report success in making electrical contact to individual magnetic N@C(60) molecules and measuring spin excitations in their electron tunnelling spectra. We verify that the molecules remain magnetic by observing a transition as a function of magnetic field that changes the spin quantum number and also the existence of non-equilibrium tunnelling originating from low-energy excited states. From the tunnelling spectra, we identify the charge and spin states of the molecule. The measured spectra can be reproduced theoretically by accounting for the exchange interaction between the nitrogen spin and electron(s) on the C(60) cage.     

Investigation of the effects of a variation of fuel assembly position on the ex-core neutron flux detection in a PWR

This work shows the impact of potential displacements of the fuel assembly positions in the reactor core on the signal values of the ex-core instrumentation of a pressurized water reactor in order to understand in detail the impact on the calibration factor of ex-core detectors. This was done with a range of Monte Carlo calculations that simulated the detailed geometrical effect by stepwise changing of the positions of fuel assemblies for selected, conservative scenarios. First, criticality calculations were carried out for the chosen core configurations, and corresponding surface sources on the core barrel were determined. In these calculations, the distances were varied between the fuel assemblies which were in the line of sight of the ex-core instrumentation. A maximal change of the fluxes on the surface of the core barrel of 4%/mm could be calculated under conservative assumptions for the combination of displaced fuel assemblies. In addition, a dependence of this effect as a function of cycle burn-up was analyzed. In a second step, transport calculations for the ionization chambers were performed using the surface sources. An increase of the reaction rate at the chambers of up to 3%/mm has been calculated.     

Metal Organic Frameworks for Natural Gas Storage in Vehicles

With the increasing demand for alternative fuels the storage of natural gas (NG) in adsorbents like metal organic frameworks (MOFs) will become more important. In order to use MOFs as storage media in fuel delivery systems, the optimization of mass and energy transfer of the system is crucial. For rapid NG filling of a tank, molecules need to reach the adsorption sites within a reasonable time while the heat of adsorption should be dissipated to the environment. In this article, mass transfer in shaped bodies of MOFs was determined by permeability measurements and pulsed field gradient (PFG) NMR spectroscopy. The heat dissipation was also experimentally measured and both data sets were used to set up a theoretical density function theory model to predict the behavior of MOFs for NG storage.     

Experimental fire analysis of steel‐to‐timber connections using dowels and nails

The paper describes and discusses the results of an extensive testing programme on the structural behaviour of timber connections under ISO‐fire. The results of reference tests performed at normal temperature are also presented. From the variety of timber connections multiple shear steel‐to‐timber connections with dowels and slotted‐in steel plates and connections with steel side plates and annular ringed shank nails were experimentally studied. Particular attention was given to the analysis of the efficiency of different strategies in order to increase the fire resistance of the timber connections. The test results showed that unprotected multiple shear steel‐to‐timber connections with dowels designed for normal temperature reached a fire resistance of about 30 min. A reduction of the load level applied during the fire did not lead to a significant increase of the fire resistance. By increasing the side timber members as well as the end distance of the dowels by 40 mm the connections reached a fire resistance of more than 70 min. Connections protected by timber boards or gypsum plasterboards showed a fire resistance of around 60 min. Thus, from a fire design point of view these strategies were favourable in order to increase the fire resistance of the connections significantly. Unprotected connections with steel side plates and annular ringed shank nails failed already after about 12 min due to large deformations of the nails and the steel side plates directly exposed to fire. By protecting the steel side plates using an intumescent paint the fire resistance of the connections was increased to around 30 min. The test results enlarged the experimental background of timber connections in fire significantly. Copyright © 2009 John Wiley & Sons, Ltd.     

A Systematic Structure–Activity Study of a New Type of Small Peptidic Transfection Vector Reveals the Importance of a Special Oxo-Anion-Binding Motif for Gene Delivery

We discovered a new class of artificial peptidic transfection vectors based on an artificial anion-binding motif, the guanidiniocarbonylpyrrole (GCP) cation. This new type of vector is surprisingly smaller than traditional systems, and our previous work suggested that the GCP group was important for promoting critical endosomal escape. We now present here a systematic comparison of similar DNA ligands featuring our GCP oxo-anion-binding motif with DNA ligands only consisting of naturally occurring amino acids. Structure–activity studies showed that the artificial binding motif clearly outperformed natural amino acids such as histidine, lysine, and arginine. It improved the ability to shuttle foreign genetic material into cells, yet successfully mediated endosomal escape. Also, plasmids that were complexed by our artificial ligands were stabilized against cytosolic degradation to some extent. This resulted in the successful expression of plasmid information (comparable to gold standards such as polyethyleneimine). Hence, our study clearly demonstrates the importance of the tailor-made GCP anion-binding site for efficient gene transfection.     

Design of LTCC with High Thermal Expansion

New applications of low-temperature co-fired ceramics (LTCC), such as pressure sensors or integrated functional layers, require materials that possess higher coefficients of thermal expansion (CTE). To fabricate LTCC with elevated CTE, two methods of material design are examined: firstly, glass ceramic composites (GCC), which consist of >50 vol% glass in the starting powder, and, secondly, glass-bonded ceramics (GBC), where glass is added as a sintering aid only. The CTE of GBC is mainly determined by the crystalline component. For GCC, the CTE can be well predicted, if CTE and elastic data of each phase in the microstructure are known. A nonlinear characteristic of the CTE versus phase composition was found with increasing E _crystals/ E _glass ratio and absolute CTE difference between the components. The glass composition and glass amount can be used to compensate the fixed properties of a crystalline material in a desired way. However, because the CTE and permittivity of a glass cannot be chosen independently, an optimum glass composition has to be found. For a given LTCC, it is possible to control the devitrification by shifting the glass composition. In this way, the resulting CTE values can be predicted more exactly and tailoring becomes possible. Different LTCC materials, based on the crystalline compounds Ba(La,Nd)₂Ti₄O₁₂, ZrO₂ (Y-TZP), SiO₂ (quartz), and specially developed glasses, possessing an elevated CTE of around 10 × 10⁻⁶ K⁻¹ while showing permittivity ɛ_r between 6 and 63, are introduced.