Experimental evidence for impulsive energy transfer in electronically adiabatic low-energy collison of Na+ with CF4

Time-of-flight measurement of the inelastic scattering of Na⁺ ions from CF₄ reveal two energy-loss mechanisms which have been observed at center-of-mass collison energies between 4 and 24 eV. At small angles θ_1ab?20° a single energy transfer peak is observed and attributed to normal mode excitation. At larger angles an additional sharp peak is observed out to θ_lab = 70° with nearly double the energy transfer. the final velocities and angular dependence agree with an impulsive interaction involving only one of the F atoms with an effective mass which approaches that of the F atoms with increasing collison energy. This is the first evidence for an impulsive mechanism in inelastic collisons at energies below the threshold for electonic excitation.     

Elementaranalyse auf nassem Wege

Ohne Zusammenfassung     

Distance dependence of the local density of states in the near field of a disordered plasmonic film

We measure the statistical distribution of the photonic local density of states in the near field of a semicontinuous gold film. By varying the distance between the measurement plane and the film, we show that near-field confined modes play a major role in the width of the distribution. Numerical simulations in good agreement with experiments allow us to point out the influence of nonradiative decay channels at short distance.     

Independence in Operator Algebras

Various notions of independence of observables have been proposed within the algebraic framework of quantum field theory. We discuss relationships between these and the recently introduced notion of logical independence in a general operator-algebraic context. We show that C^*-independence implies an analogue of classical independence.     

Competitive Destabilization/Stabilization of β‐Lactoglobulin Foam by PEO‐PPO‐PEO Polymeric Surfactants

The effect on β‐lactoglobulin foamability and foam stability of the poly(ethylene oxide)‐poly(propylene oxide) block copolymers F127 (PEO₉₉‐PPO₆₅‐PEO₉₉), molecular weight 12500 g/mol, and P85 (PEO₂₆‐PPO₃₉‐PEO₂₆), molecular weight 4600 g/mol, has been investigated at constant protein concentration, 10 µM (0.2 mg/L), and varying block copolymer concentrations, ranging from 0.02 to 1600 µM. Foam was generated by means of air sparging and the foam volume and liquid volume of the foam were measured for one hour. It was found that foam stabilized by F127 or P85 in the concentration range 20–1600 µM contained a larger liquid volume initially than pure β‐lactoglobulin foam. Furthermore, β‐lactoglobulin foamability was only marginally affected by the presence of F127, while it was reduced in an interval of low P85 concentrations. The protein foam stability was retained in the presence of the larger polymer F127, whereas P85 largely reduced the stability, indicating that the size of the polymeric surfactant is important. The results are discussed in relation to surface rheological properties and forces acting across foam films. Steric repulsion generated between the surfaces of foam films is suggested to be the main stabilizing factor in dry foam containing F127. The instability of the mixed β‐lactoglobulin/P85 system is suggested to be caused by two effects. First, there are incompatible stabilization mechanisms of block copolymer and protein, as supported by previous surface rheological data. Second, there is a reduced importance of long‐range steric repulsion when P85 is added, compared to the case where F127 and β‐lactoglobulin are mixed.     

Heat capacity of Pd40Ni40P20 in the deeply undercooled liquid state determined by relaxation experiments in the glass transition region

An indirect method is presented which allows for the heat capacity determination of deeply undercooled melts at temperatures in the glass transition region, which are inaccessible to continuous calorimetric measurements. The method is based only on the unique relaxation behavior of glass-forming liquids in the transition region, and thus is generally applicable for vitreous systems. Here it is illustrated by measurements of the specific heat of deeply undercooled Pd₄₀Ni₄₀P₂₀, a metallic bulk-glass former, resulting in a considerable approach of the measurements towards the isentropic limit. Additionally, the consequent application of this method allowed for the determination of the dependence of the glass temperature on the cooling rate during vitrification, yielding a linear relation between the glass temperature and the logarithm of the cooling rate, as observed for several non-metallic glass-forming systems.