A monopole mass filter with a hyperbolic V-shaped electrode

In this article we compare the classical monopole mass filter of von Zahn and the monopole mass filter with a hyperbolic V-shaped electrode. The experimental results and those of computer simulation for both mass spectrometers are presented. We show that the replacement of a conventional 90 degrees V-shaped electrode by an electrode with a hyperbolic profile substantially improves the peak shape of any given mass, and increases the mass resolution by a factor of 3-4 and the abundance sensitivity by a factor of 100. The potential of high analytical performance combined with electroforming techniques for electrode manufacture indicate future practical uses of such instruments. Copyright 1999 John Wiley & Sons, Ltd.     

A three body approach to study the structural properties of 2-n halo nuclei and the search for Efimov states

The discovery of neutron rich isotopes of the lightest elements on the neutron drip line exhibiting a halo structure has opened up new vistas in research activities. The novel structural features associated with the halo phenomena have been the subject for extensive theoretical and experimental investigations in recent times. In this talk, I propose to present a broad overview of the recent developments in this field, bringing out the striking features which show that a large number oflight nuclei near the neutron drip line are characterized by a clear separation between a ‘normal’ core nucleus and a loosely bound low density veil of neutrons. Specifically, the two neutron halos offer a natural premises, from a theoretical standpoint, to employ three body techniques for studying their detailed structural properties. A considerable part of the talk will be devoted to report and highlight the results on a number of light halo nuclei such as ¹¹Li, ¹¹Be, ¹⁹B and ²²C on which we have been carrying out investigations employing a simple but realistic three body model. These three body systems which have been termed as ‘Borromean’ (i.e while three body systems are bound, the corresponding binary subsystems on the other hand are unbound) are characterized by large spacial extension and very low separation energy of the neutron. They are, therefore, ideally suited for exploring the possibility of the existence of Efimov states in two neutron halo nuclei. We have recently carried out the three body analyses to predict the possibility of the occurrence of such states on which experimental work at various laboratories is underway.     

Shape resonances in slow electron scattering by aromatic molecules. I. Anthraquinone derivatives

A series of anthraquinone (C(14)O(2)H(8)) derivatives has been studied by means of electron capture negative ion mass spectrometry (ECNI-MS), photoelectron spectroscopy (PES), and AM1 quantum chemical calculations. Mean lifetimes of molecular negative ions M(-.) (MNI) have been measured. The mechanism of long-lived MNI formation in the epithermal energy region of incident electrons has been investigated. A simple model of a molecule (a spherical potential well with the repulsive centrifugal term) has been applied for the analysis of the energy dependence of cross sections at the first stage of the electron capture process. It has been shown that a temporary resonance of MNI at the energy approximately 0.5 eV corresponds to a shape resonance with lifetime 1-2.10(-13) s in the f-partial wave (l = 3) of the incident electron. The next resonant state of MNI at the energy approximately 1.7 eV has been associated with the electron excited Feshbach resonance (whose parent state is a triplet npi* transition). In all cases the initial electron state of the MNI relaxes into the ground state by means of a radiationless transition, and the final state of the MNI is a nuclear excited resonance with a lifetime measurable on the mass spectrometry timescale. Copyright 1999 John Wiley & Sons, Ltd.     

Functional group dependent site specific fragmentation of molecules by low energy electrons

Functional group dependence is observed in the dissociative electron attachment (DEA) to various organic molecules in which the DEA features seen in the precursor molecules of the groups are retained in the bigger molecules. This functional group dependence is seen to lead to site-selective fragmentation of these molecules at the hydrogen sites. The results are explained in terms of the formation of core-excited Feshbach resonances. The results point to a simple way of controlling chemical reactions as well as interpreting the DEA data from bigger biological molecules.     

Functional group dependent dissociative electron attachment to simple organic molecules

Dissociative electron attachment (DEA) cross sections for simple organic molecules, namely, acetic acid, propanoic acid, methanol, ethanol, and n-propyl amine are measured in a crossed beam experiment. We find that the H(-) ion formation is the dominant channel of DEA for these molecules and takes place at relatively higher energies (>4 eV) through the core excited resonances. Comparison of the cross sections of the H(-) channel from these molecules with those from NH(3), H(2)O, and CH(4) shows the presence of functional group dependence in the DEA process. We analyze this new phenomenon in the context of the results reported on other organic molecules. This discovery of functional group dependence has important implications such as control in electron induced chemistry and understanding radiation induced damage in biological systems.     

Markovian representation of a bilinear time series model and maximum likelihood estimation of the parameters

A bilinear time series (BLTS) model is expressed in the form of Akaike's Markovian representation in order to use the Kalman recursive estimation approach. It is shown that Akaike's Markovian representation of autoregressive moving average models of orderp and q (ARMA(p,q)) and that of the bilinear model are equivalent. This equivalence facilitates the maximum likelihood estimation of the parameters involved in the bilinear model, which otherwise is an unwieldy problem. The present approach can easily be extended to take into account missing observations     

Simultaneous quantitation of IC87114, roflumilast and its active metabolite roflumilast N‐oxide in plasma by LC‐MS/MS: application for a pharmacokinetic study

A sensitive and reliable high‐performance liquid chromatography–mass spectrometry (LC–MS/MS) was developed and validated for simultaneous quantification IC87114, roflumilast (RFM), and its active metabolite roflumilast N‐oxide (RFN) using tolbutamide as an internal standard. The analytes were extracted by using liquid–liquid extraction and separated on a reverse phase C₁₈ column (50 mm × 3 mm i.d., 4.6 µ) using methanol: 2 mM ammonium acetate buffer, pH 4.0 as mobile phase at a flow rate 1 mL/min in gradient mode. Selective reaction monitoring was performed using the transitions m/z 398.3 > 145.9, 403.1 >186.9, 419.1 > 187.0 and 271.1 > 155.0 to quantify quantification IC87114, RFM, RFN and tolbutamide, respectively. The method was validated over the concentration range of 0.1–60 ng.mL^?1 for RFM and RFN and 6 to 2980 ng.mL^?1 for IC87114. Intra‐ and inter‐day accuracy and precision of validated method were within the acceptable limits of <15% at all concentrations. Coefficients of correlation (r²) for the calibration curves were >0.99 for all analytes. The quantitation method was successfully applied for simultaneous estimation of IC87114, RFM and RFN in a pharmacokinetic drug–drug interaction study in Wistar rats. Copyright © 2012 John Wiley & Sons, Ltd.     

Effect of Surface Passivation in Spinel Slurry Toward Hydrolysis: Neutron Scattering and Rheological Studies

Aqueous colloidal forming of magnesium aluminate (MgAl₂O₄) spinel offers much potential for various applications; however, these advantages are generally offset by the basic nature of the powder and its affinity for hydrolysis. Hydrolysis in the presence of water generally imparts surface chemical changes resulting in the degradation of colloidal stability. In the present study, spinel powders were subjected to thermally assisted surface passivation and evaluated for the effectiveness of preventing hydrolysis through quasielastic neutron scattering (QENS) technique and correlated with rheological measurements. In order to evaluate the extent of hydrolysis, spinel slurries prepared with (SP) and without surface passivation (WSP) were studied by rheological and QENS measurements at regular intervals of time. While WSP slurry exhibited a steep enhancement in viscosity from 1.02 to 19.4 Pa · s and fraction of the elastic intensity from 0.20 to 0.38 for 96 and 200 hours, respectively, a negligible change in viscosity for SP slurries from 0.313 to 0.345 Pa · s and fraction of the elastic intensity from 0.16 to 0.17 for the similar period confirmed the inhibition of hydrolysis, revealing change in surface chemistry due to hydrolysis. Microscopic details as obtained from neutron scattering data revealed that dynamical behavior of water molecules in both the slurries could be described very well by the Singwi–Sjolander model of jump diffusion. Further analysis showed lower diffusivity ～1.82 × 10^?5 cm²/sec and higher residence time ～6.39 ps for WSP slurry in comparison with 2.16 × 10^?5 cm²/sec and 5.80 ps, complimenting the inhibition of hydrolysis in case of SP slurry.