Dimerization of some substituted benzoic acids in aqueous solution from conductance measurements

Precision molar conductances of benzoic, o-toluic, 2,6-dimethylbenzoic, 2,3,6-trimethylbenzoic, and, o-fluorobenzoic acids have been determined in aqueous solution as a function of temperature and of concentration up to near saturation (<0.035 M). At the higher concentrations molar conductances are found to be less than anticipated for the simple dissociation of a 1-1 electrolyte. Although the deviations are only 1% or less they have been interpreted to show that these acids are dimerized in solution. The interpretation includes an assumption that the dimer ionizes to produce a triple ion. Increasing numbers of methyl groups lead to increasing dimerization. For those acids with two ortho groups the dimerization increases with increasing temperature while the other three show decreasing dimerization with increasing temperature. Temperature functions have been determined for the dimerization constants and from these functions standard changes in enthalpy, entropy, and heat capacity have been determined. Comparisons are made with dimerization studies in non-aqueous solvents. From these as well as the behavior of benzene in water it is concluded that a major factor driving the dimerization is hydrophobic interaction. To provide a limiting conductance of the triple ion needed in the dimerization calculations a conductance study was also made for o-Phenylbenzoic acid on the assumption that its anion provides an approximate model of the triple ion.     

A measurement of differential cross-sections and nucleon structure functions in charged-current neutrino interactions on iron

A high-statistics measurement of the differential cross-sections for neutrino-iron scattering in the wide-band neutrino beam at the CERN SPS is presented. Nucleon structure functions are extracted and theirQ ² evolution is compared with the predictions of quantum chromodynamics.     

Are there “prompt” like-sign dimuons?

From exposures of the CDHS detector at the CERN SPS we have obtained 367μ ⁺ μ ^? events in neutrino beams and 73μ ⁺ μ ⁺ events in an antineutrino beam. The magnitude of a prompt like-sign signal has been controversial in the past and moreover could not be explained by known production mechanisms. A critical discussion of the experimental situation is given. We have tried to reduce the systematic uncertainties of previous experiments and to get more information on the dependence of the signal with energy and the muon momentum cut-off. This experiment yields a signal of 2.8σ (2.4σ) of prompt like-sign dimuon events in the case of neutrinos (antineutrinos). The rate to charged current events is of the order of 10^?4 forp _μ<9GeV andE>100 GeV. The prompt signal has all the properties expected from the production and decay of charm-anticharm events. The magnitude, however, is substantially higher then the prediction of perturbative QCD but lower than some other experiments.     

Electroweak parameters from a high statistics neutrino nucleon scattering experiment

The final results from the WA 1/2 neutrino experiment in the 1984 CERN 160 GeV narrow band beam are presented. The ratiosR _ν and \(R_{\bar v} \) of neutral to charged current interaction rates of neutrinos and antineutrinos in iron are measured to beR _ν=0.3072±0.0033 and \(R_{\bar v} \) =0.382±0.016. A value of the electroweak parameter sin² θ _w = 1 ?m _W ² /m _Z ² is extracted fromR _ν. The result is sin² θ _w =0.228+0.013(m _c ?1.5)±0.0003 (theor.) wherem _c is the mass of the charmed quark in GeV form _t =60 GeV,M _H =100 GeV, ρ=1. CombiningR _ν and \(R_{\bar v} \) one obtains a value for ρ=0.991+0.023(m _c ?1.5)±0.020(exp.). Alternatively,R _ν and \(R_{\bar v} \) yield a precise value of the ratio of intermediate vector boson massesm _W /m _Z =0.880?0.007(m _c ?1.5)±0.002(exp.)±0.002(theor.). Comparison of these results with those from direct measurements of the vector boson masses are presented. In a model-independent analysis the left- and right-handed neutral current coupling constants,g _L ² andg _R ² , are determined.     

Method for rapid metabolite profiling of drug candidates in fresh hepatocytes using liquid chromatography coupled with a hybrid quadrupole linear ion trap

Rapid information on metabolic profiling is required to evaluate the structural liabilities of drug candidates in early drug discovery. In this study, a sensitive and rapid semi-quantitative method was developed to simultaneously monitor the drug candidate and metabolites as well as collect tandem mass (MS/MS) spectra for subsequent metabolite identification. The simultaneous semi-quantitation and identification of metabolites in fresh hepatocytes is achieved using high-performance liquid chromatography (HPLC) coupled with a hybrid quadrupole linear ion trap. The survey experiment consists of monitoring multiple-reaction monitoring (MRM) transitions for the internal standard, the parent, and 48 MRM transitions designed to cover the most common phase I and II biotransformations. An information-dependent acquisition (IDA) method was employed to trigger product ion scans above the MRM signal threshold. Three biotransformations of a lead compound have been identified through enhanced product ion scans and the respective MRM transitions of those metabolites were selected for semi-quantitation. Parent disappearance and formation of the metabolites as a function of incubation time in five different species were monitored by their respective MRM responses. The method provides the necessary sensitivity to detect minor metabolites in a relevant therapeutic concentration range. Enzymatic turnover of the parent and the metabolites in different species are revealed based on the different initial concentrations of the parent. This methodology integrates the parent disappearance, metabolite identification, and the formation of the metabolites along the time course using a single rapid LC/MS/MS analysis. This method can be used as a complementary tool to the conventional method of metabolic profiling. It provides a rapid and sensitive initial profile of the metabolism of potential structural series at the lead selection stage. The method can also be incorporated into the overall metabolite profiling scheme to evaluate the drug candidates in drug discovery.     

Dissolution of Platinum Single Crystals in Acidic Medium

Platinum single crystal basal planes consisting of Pt(111), Pt(100), Pt(110) and reference polycrystalline platinum Pt(poly) were subjected to various potentiodynamic and potentiostatic electrochemical treatments in 0.1 M HClO₄. Using the scanning flow cell coupled to an inductively coupled plasma mass spectrometer (SFC-ICP-MS) the transient dissolution was detected on-line. Clear trends in dissolution onset potentials and quantities emerged which can be related to the differences in the crystal plane surface structure energies and coordination. Pt(111) is observed to have a higher dissolution onset potential while the generalized trend in dissolution rates and quantities was found to be Pt(110)>P(100)≈Pt(poly)>Pt(111).     

Wärmestrahlungsverhalten von Gas-/Feststoffgemischen bei niedrigen,mittleren und hohen Staubbeladungen

Zusammenfassung Zur Simulation des Wärmestrahlungsverhaltens staubbeladener Strömungen wurde ein Berechnungsmodell auf physikalischer Basis entwickelt, welches die Auswirkungen von Absorption, Vorwärts- und Rückwärtsstreuungen berücksichtigt. Neu gegenüber herkömmlichen Verfahren ist, daß die hierbei benötigten optischen Koeffizienten nicht empirisch oder durch Messungen ermittelt werden, sondern über die Anwendung der Mie-Theorie explizit berechenbar sind. Aufgrund der Erfassung der Rückwärtsstreuung ist das Modell zur Behandlung höherer Staubbeladungen bis in den Grenzbeeich der stationären Wirbelschicht geeignet.

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Thermal radiation of gas/solid mixtures with low, medium and high particle loadings

To describe the thermal radiation behaviour of particle-laden flows a mathematical model, based on a physical approach, was developed which takes into account the effects of absorption, scattering and backscattering. In contrast to existing calculational methods the required optical coefficients are not obtained empirically or by measurement. By applying the Mie theory these parameters can be calculated in an explicit manner. As backscattering is taken into consideration, the model is suitable for applications even at very high particle loadings including the limiting case of stationary fluidized beds.