Studies of the out-of-plane emission of pions in symmetric heavy-ion collisions

Triple differential cross-sections of midrapidity pions from ²⁰⁹Bi+²⁰⁹Bi collisions were measured with the Kaon Spectrometer at SIS at incident energies of 400, 700 and 1000 AMeV. The azimuthal emission pattern of the pions has been investigated in dependence of beam energy and impact parameter. An enhanced emission of pions perpendicular to the reaction plane is observed. The strength of the anisotropy increases with beam energy and pion transverse momentum. In contrast to the nucleons the anisotropy varies only little with the impact parameter. No difference in the behaviour of positive and negative pions is observed.     

End-to-end correlation for a C-12 hydrocarbon chain

The 19F nuclear spin-lattice relaxation rate constants were measured as a function of magnetic field strength for 1,12-diaminododecane labeled at one end with a nitroxide radical and at the other with a trifluoromethyl group. The magnetic relaxation dispersion profile (MRD) reports the spectral density function appropriate to the end-to-end correlation function for the doubly labeled molecule. After extrapolation to zero concentration to eliminate the intermolecular relaxation contribution to relaxation, the resulting intramolecular MRD profile was compared with several model approaches. The rotational model for the spectral density functions as included in the Solomon-Bloembergen-Morgan equations does not describe the data well. The earlier model of Freed for nuclear spin relaxation induced by a freely diffusing paramagnetic co-solute is not rigorous for this case because the paramagnet is tethered to the observed nuclear spin and only a restricted space in the immediate vicinity of the nuclear spin is accessible for pseudo-translational diffusion of one end of the molecule with respect to the other. A generalization of the Torrey model for magnetic relaxation by translational diffusion developed by Nevzorov and Freed, which includes the effect of restrictions imposed by the finite length of the chain, describes the experiment within experimental errors. A simple modification of the Hwang-Freed model that does not specifically include the dynamical effects of the finite tether also provides a good approximation to the data when the tether chain is sufficiently long.     

Correspondence between spin-dynamic phases and pulse program phases of NMR spectrometers

Spin state selective experiments have become very useful tools in solution NMR spectroscopy, particularly in the context of TROSY line narrowing. However, the practical implementation of such pulse sequences is frequently complicated by unexpected instrument behavior. Furthermore, a literal theoretical analysis of sequences published with specific phase settings can fail to rationalize such experiments and can seemingly contradict experimental findings. In this communication, we develop a practical approach to this ostensible paradox. Spin-dynamic design, rationalization, and simulation of NMR pulse sequences, as well as their confident and reliable implementation across current spectrometer hardware platforms, require precise understanding of the underlying nutation axis conventions. While currently often approached empirically, we demonstrate with a simple but general pulse program how to uncover these correspondences a priori in the general case. From this, we deduce a correspondence table between the spin-dynamic phases used in NMR theory and simulation on the one hand and pulse program phases of current commercial spectrometers on the other. As a practical application of these results, we analyze implementations of the original (1)H-(15)N TROSY experiment and illustrate how steady-state magnetization can be predictably, rather than empirically, added to a desired component. We show why and under which circumstances a literal adoption of phases from published sequences can lead to incorrect results. We suggest that pulse sequences should be consistently given with spin-dynamically correct (physical) phases, rather than in spectrometer-specific (software) syntax.     

Formant transitions in fricative identification: the role of native fricative inventory

The distribution of energy across the noise spectrum provides the primary cues for the identification of a fricative. Formant transitions have been reported to play a role in identification of some fricatives, but the combined results so far are conflicting. We report five experiments testing the hypothesis that listeners differ in their use of formant transitions as a function of the presence of spectrally similar fricatives in their native language. Dutch, English, German, Polish, and Spanish native listeners performed phoneme monitoring experiments with pseudowords containing either coherent or misleading formant transitions for the fricatives /s/ and /f/. Listeners of German and Dutch, both languages without spectrally similar fricatives, were not affected by the misleading formant transitions. Listeners of the remaining languages were misled by incorrect formant transitions. In an untimed labeling experiment both Dutch and Spanish listeners provided goodness ratings that revealed sensitivity to the acoustic manipulation. We conclude that all listeners may be sensitive to mismatching information at a low auditory level, but that they do not necessarily take full advantage of all available systematic acoustic variation when identifying phonemes. Formant transitions may be most useful for listeners of languages with spectrally similar fricatives.     

Nuclear stopping from 0.09A to 1.93A GeV and its correlation to flow

We present a complete systematics (excitation functions and system-size dependences) of global stopping and side flow for heavy ion reactions in the energy range between 0.09A and 1.93A GeV. For the heaviest system, Au+Au, we observe a plateau of maximal stopping extending from about 0.2A to 0.8A GeV with a fast drop on both sides. The degree of stopping, which is shown to remain significantly below the expectations of a full stopping scenario, is found to be highly correlated to the amount of side flow.     

A57Fe Mössbauer study of the high pressure hydride phases of Fe and Co

Hydrides of iron and cobalt prepared at pressures between 4.0 and 9.5 GPa were studied by⁵⁷Fe Mössbauer spectroscopy at 4.2 K. Iron hydride was found to be nearly stoichiometric FeH. The two iron sites in its dhep lattice have hyperfine fields of 33.8 and 28.8 T. Practically the same results were found for the deuteride. In hep ε-CoH_x, the hyperfine fields decrease with hydrogen content by about 6% betweenx=0 andx=0.5. In all studied hydrides the electron densities at the⁵⁷Fe nuclei are smaller than in the pure metals.     

A193Ir Mössbauer study of Pt−Ir catalysts prepared by impregnantion of silica with H2MCl6

The state of iridium on Pt?Ir catalysts prepared by impregnation of amorphous silica with H₂IrCl₆ and H₂PtCl₆ was studied by¹⁹³Ir Mössbauer spectroscopy after different steps of preparation. The Ir is adsorbed in its trivalent state, presumably as [IrCl₆]^3?. Calcination in air at 450°C converts this to IrO₂. The metallic clusters formed by subsequent reduction in H₂ at 200°C show a strong tendency towards segregation of Ir and Pt and re-oxidize partially when exposed to air at ambient temperature. In both respects the behaviour is similar to that of samples prepared by co-exchange from [Ir(NH₃)₅Cl]Cl₂ and Pt(NH₃)₄Cl₂. H₂O.     

A CEMS apparatus for in situ studies of ion beam modified metals

An apparatus for CEMS studies of ion beam modified metals is described. The spectrometer can be coupled directly to the ion implanter. During ion bombardement the sample can be cooled to liquid nitrogen temperature or heated to about 500 K. CEMS measurements can be taken directly after ion beam modification between room temperature and liquid nitrogen temperature. As a first test of the performance of the apparatus CEMS spectra of boron-ion implanted iron at room temperature are presented.     

F-18-FDG uptake is a reliable predictory of functional recovery of akinetic but viable infarct regions as defined by magnetic resonance imaging before and after revascularization

Identification of akinetic but viable myocardium is important for the selection of patients for coronary revascularization. In order to assess predictive values of end-diastolic wall thickness and dobutamine induced wall thickening obtained by magnetic resonance imaging (MRI) and [18F]Fluorodeoxyglucose uptake assessed by positron emission tomography (F-18-FDG-PET), these parameters were compared to recovery of left ventricular function after successful revascularization. Forty patients with chronic myocardial infarction and regional a- or dyskinesia by ventriculography underwent rest- and dobutamine-MRI studies (10 microg dobutamine/kg body weight/min) and F-18-FDG-PET. Viability of the infarct region was considered to be present if; 1) end-diastolic wall thickness was > or =5.5 mm; 2) dobutamine induced wall thickening > or =2 mm could be measured; and 3) normalized F-18-FDG-uptake was > or =50% in > or =50% of akinetic segments. Preserved end-diastolic wall thickness was found in 32/40 patients, functional improvement during dobutamine infusion in 26/40 patients and preserved F-18-FDG-uptake in 29/40 patients. After revascularization regional left ventricular function improved in 25/40 patients. Positive and negative predictive values and diagnostic accuracy were 78%, 100%, and 83% for preserved end-diastolic wall thickness, 92%, 93%, and 93% for dobutamine inducible contraction reserve and 86%, 100%, and 90% for preserved F-18-FDG-uptake. Quantitative assessment of dobutamine induced systolic wall thickening by MRI and F-18-FDG-uptake by PET are highly accurate techniques for the identification of viable myocardium and prediction of functional recovery after successful revascularization. Preserved end-diastolic wall thickness results in an overestimation of viable myocardium compared to functional improvement, but wall thickness <5.5 mm excludes recovery of regional function.