Scaling and suppression of anomalous heating in ion traps

We measure and characterize anomalous motional heating of an atomic ion confined in the lowest quantum levels of a novel rf ion trap that features moveable electrodes. The scaling of heating with electrode proximity is measured, and when the electrodes are cooled from 300 to 150 K, the heating rate is suppressed by an order of magnitude. This provides direct evidence that anomalous motional heating of trapped ions stems from microscopic noisy potentials on the electrodes that are thermally driven. These observations are relevant to decoherence in quantum information processing schemes based on trapped ions and perhaps other charge-based quantum systems.     

On a Simple Nonisothermal Adsorption Experiment with Organic Vapors and an Inertial Microbalance To Study the Surface Properties of Hybrid (Organic/Inorganic) Porous Materials

A nonisothermal adsorption experiment using a controlled flow of cyclopentane in the 333-313 K range is used to simultaneously estimate the specific surface area and micropore volume of a hybrid (organic/inorganic) alcogel. For reference, the method is also applied to an all-inorganic material with a more rigid structure, namely, a high surface area SiO(2)-Al(2)O(3). The proposed data analysis provides guidelines to determine whether adsorption data on a certain adsorbate/adsorbent system can be modeled effectively as a convolution of BET (meso- and macropore) and Dubinin-Radushkevitch (DR, micropore) contributions. Copyright 2000 Academic Press.     

Working group report: Heavy-ion physics and quark-gluon plasma

This is the report of Heavy Ion Physics and Quark-Gluon Plasma at WHEPP-09 which was part of Working Group-4. Discussion and work on some aspects of quark-gluon plasma believed to have created in heavy-ion collisions and in early Universe are reported.     

Meson production in p + d reactions

Total and differential cross sections for the reactions p + d → ³He + m ⁰ with m=π, η and p + d → ³H+π⁺ were measured with the GEM detector at COSY for beam momenta between threshold and the maximum of the corresponding baryon resonance. For both reactions a strong forward-backward asymmetry was found. The data were compared with model calculations. The aspect of isospin symmetry breaking is studied. Representing the GEM Collaboration     

Interaction between explosive and analyte layers in explosive matrix-assisted plasma desorption mass spectrometry

An HMX/insulin two-layer system was chosen as a model for further investigation of the matrix properties of explosive materials for protein analytes in plasma desorption mass spectrometry. The dependencies of the molecular ion yield and average charge state as a function of the analyte thickness were studied. An increase in the charge state of multiply protonated molecular species was confirmed as the major matrix effect, with the average charge state z at the smallest thickness studied being higher than in matrix-assisted laser desorption/ionization and closer to the value obtained in electrospray ionization under standard acidic conditions. Observed charge state distributions are significantly narrower than the corresponding Poisson distributions, which suggests that the protonation of insulin is limited in plasma desorption by the number of basic sites in the molecule, similar to electrospray ionization. Both the curve displaying total molecular ion yield and the one showing the total charge (proton) yield as a function of the insulin thickness have maxima at a thickness different from an insulin monolayer. These observations diminish the significance of a matrix/analyte interface mechanism for the explosive matrix assistance. Instead, a mechanism related to the chemical energy release during conversion of the explosive after the ion impact is proposed. As additional mechanisms, enhanced protonation of the analyte through collisions with products of the explosive decay is considered, as well as electron scavenging by other products, which leads to a higher survival probability of positively charged protein molecular ions. Copyright 1999 John Wiley & Sons, Ltd.     

Spectral and Spatial UV Sky Radiance Measurements at a Seaside Resort Under Clear Sky and Slightly Overcast Conditions

Spatial measurements of the diffusely scattered sky radiance at a seaside resort under clear sky and slightly overcast conditions have been used to calculate the sky radiance distribution across the upper hemisphere. The measurements were done in the summer season when solar UV radiation is highest. The selected wavelengths were 307, 350 and 550 nm representing the UVB, UVA and VIS band. Absolute values of radiance differ considerably between the wavelengths. Normalizing the measured values by use of direct solar radiance made the spatial distributions of unequal sky radiance comparable. The results convey a spatial impression of the different distributions of the radiance at the three wavelengths. Relative scattered radiance intensity is one order of magnitude greater in UVB than in VIS, whereas in UVA lies roughly in between. Under slightly overcast conditions scattered radiance is increased at all three wavelengths by about one order of magnitude. These measurements taken at the seaside underline the importance of diffuse scattered radiance. The effect of shading parts of the sky can be estimated from the distribution of sky radiance. This knowledge might be useful for sun seekers and in the treatment of people staying at the seaside for therapeutic purposes.     

Synthesis,NMR spectra and chromatographic properties of five trimethylarsonioribosides

Five trimethylarsonioribosides were prepared from naturally occurring and synthetic dimethylarsinylribosides (arsenosugars) by reducing them with 2,3-dimercaptopropanol and quaternizing the resultant arsine with methyl iodide. The trimethylarsonioribosides prepared in this manner were the four novel compounds methyl 5-deoxy-5-trimethylarsonio-β-D -riboside (as the iodide), (2′R)-2′, 3′-dihydroxypropyl 5-deoxy-5-trimethylarsonio-β-D -riboside (as the formate), 3′-[(2″, 3″ -dihydroxypropyl)hydroxyphosphinyloxy] - 2′ -hydroxypropyl 5-deoxy-5-trimethylarsonio-β-D -riboside and 3-(5′-deoxy-5′-trimethylarsonio-β-D -ribosyloxy)-(2S)-2-hydro xypropanesulfonate, and the known (2′S)-2′-hydroxy-3′-(sulfooxy)propyl 5-deoxy-5-trimethylarsonio-β-D -riboside. They were synthesized to serve as standards for chromatographic analyses of arsenic compounds in marine samples and for investigations into the biotransformation of arsenic in marine organisms. NMR spectral and chromatographic data for the five trimethylarsonioribosides are presented and compared with those of their dimethylarsinyl analogues.