Analysis of transverse momentum and event shape invN scattering

The transverse momentum distributions of hadrons produced in neutrino-nucleon charged current interactions and their dependence onW are analysed in detail. It is found that the components of the transverse momentum in the event plane and normal to it increase withW at about the same rate throughout the availableW range. A comparison withe ⁺ e ^? data is made. Studies of the energy flow and angular distributions in the events classified as planar do not show clear evidence for high energy, wide angle gluon radiation, in contrast to the conclusion of a previous analysis of similar neutrino data.     

Metastable peaks in a mass spectrum measured automatically under high resolution fast scan conditions

Three metastable peaks have been automatically recorded in the fast scan high resolution mass spectrum of 2-hydroxy-4-octoxybenzophenone. Values for released kinetic energy in the transitions m/e 326 to 325 and m/e 214 to 213 agree with the results obtained by conventional means.     

Spin-orbit cooling and population inversion in nozzle expansions of NH

Cooling of molecular spin-orbit fine structure in a nozzle expansion is demonstrated with a non-case (a) diatomic molecule, the A ³Π, state of NH. Not only is cooling rapid, comparable to the rate of rotational cooling, but several population inversions are observed.     

Reaction of hydroquinone with hematite; I. Study of adsorption by electrochemical-scanning tunneling microscopy and X-ray photoelectron spectroscopy

The reaction of hematite with quinones and the quinone moieties of larger molecules may be an important factor in limiting the rate of reductive dissolution, especially by iron-reducing bacteria. Here, the electrochemical and physical properties of hydroquinone adsorbed on hematite surfaces at pH 2.5-3 were investigated with cyclic voltammetry (CV), electrochemical-scanning tunneling microscopy (EC-STM), and X-ray photoelectron spectroscopy (XPS). An oxidation peak for hydroquinone was observed in the CV experiments, as well as (photo)reduction of iron and decomposition of the solvent. The EC-STM results indicate that hydroquinone sometimes forms an ordered monolayer with approximately 1.1 QH(2)/nm(2), but can be fairly disordered (especially when viewed at larger scales). XPS results indicate that hydroquinone and benzoquinone are retained at the interface in increasing amounts as the reaction proceeds, but reduced iron is not observed. These results suggest that quinones do not adsorb by an inner-sphere complex where adsorbate-surface interactions determine the adsorbate surface structure, but rather in an outer-sphere complex where interactions among the adsorbate molecules dominate.     

Reactions of polyolefins with strong lewis acids

Treatment of a cyclohexane solution of low density polyethylene and polystyrene with anhydrous aluminum chloride causes chemical reaction between the two polymers which results in the formation of a graft copolymer. The initial copolymer-forming reaction is very rapid, and prolonged contact of the polymers with aluminum chloride causes subsequent degradation in molecular weight. Treatment of separate solutions of polyethylene, isotactic polypropylene, and ethylene–propylene copolymers with aluminum chloride was studied as a function of time. The intrinsic viscosities of the polymers dropped from initial values of 2.4–6.5 to 0.55–0.85 in 5 min, followed by a slower decline over the next 2 hr. In the case of polypropylene, the low molecular weight fragments largely retained the isotactic structure, which demonstrates that stereochemical isomerization is not a major reaction.     

Baryon antibaryon production in the central region at 85 GeV/c

In a search for glueballs and exotic states decaying into baryons and antibaryons we have investigated the production of baryon antibaryon pairs produced centrally in the reactions π⁺/pp → π⁺/p(X ⁰)p at 85 GeV/c. In particular, channels whereX ⁰ goes to \(p\bar p,p\bar p\pi ^ + \pi ^ - ,p\bar p2\pi ^ + 2\pi ^ - \) and \(\Lambda \bar \Lambda \) have been observed. No significant new structure is observed in the mass spectra.     

The internal dynamic modes of charged self-assembled peptide fibrils

Photon correlation spectroscopy is used to study the internal dynamics of self-assembled charged peptide fibrils. Short neutral and charged polymeric aggregates have diffusive modes due to whole macromolecular motion. For long semiflexible fibrils the logarithm of the intermediate scattering function follows a q(2)t(3/4) scaling at long times consistent with a Kratky-Porod free energy and preaveraged Oseen hydrodynamics. Persistence lengths on the order of micrometers are calculated for the peptide fibrils consistent with estimates from the liquid-crystalline phase behavior. Fibril diameters (5-35 nm) calculated from the initial decay of the correlation functions are in agreement with transmission electron microscopy measurements.     

Azimuthal anisotropy of photon and charged parti cle emissionin 208Pb + 208Pb collisions at 158 $\ cdot A$ GeV/ c

The azimuthal distributions of photons and charged particles with respect to the event plane are investigated as a function of centrality in ²⁰⁸Pb + ²⁰⁸Pb collisions at 158 GeV/c in the WA98 experiment at the CERN SPS. The anisotropy of the azimuthal distributions is characterized using a Fourier analysis. For both the photon and charged particle distributions the first two Fourier coefficients are observed to decrease with increasing centrality. The observed anisotropies of the photon distributions compare well with the expectations from the charged particle measurements for all centralities.Received: 22 May 2004, Revised: 14 April 2005, Published online: 4 May 2005PACS: 25.75.Dw     

Analysis of chemical warfare agents III. Use of bis-nucleophiles in the trace level determination of phosgene and perfluoroisobutylene

The reactivity of phosgene and perfluoroisobutylene (PFIB) towards 1,2-bis-nucleophiles was exploited to allow determination of these gases in air samples. 2-Aminothiophenol (ATP), 3,4-dimercaptotoluene (DMT) and 2-hydroxymethylpiperidine (HMP) were evaluated as bis-nucleophiles capable of forming thermally-stable derivatives with phosgene and PFIB when loaded with triethylamine onto Tenax TA. Experimental design was used to optimise thermal desorption conditions. Detection limits in the low ngm(-3) range were observed for the five derivatives investigated. This work represents the most sensitive analytical method for trace level quantitation of phosgene and PFIB published to date.