Working Methods Paper: Critical considerations with respect to the identification of tin species in the environment

Biogeochemical pathways of tin species in the environment are still controversial, e.g. with regard to methylation and transmethylation phenomena, owing to the fact that the identification of methylated tin-compounds is often difficult. The previous tentative identification of a mixed methylbutyltin compound in sediment and biological samples by GC/AAS after hydride generation gave an illustration of this problem. This compound was previously identified in sediments by other authors and also suspected to occur in a contaminated sediment sample from the Boyardville Marina, France. The retention time obtained by GC/AAS corresponded to the actual retention time of a mixed methylbutyltin calibrant. However, additional checks demonstrated that the compound detected was actually monophenyltin. This evidence was produced by a thorough analysis of a selected sediment sample by alternative techniques such as GC/AAS and GC/AES after pentylation, GC/FPD and GC/MS. The results presented highlight the need for a full identification of compounds to avoid mis-interpretation.     

General base catalysis in the decomposition of N-Cl-Valine in aqueous solution

This article analyzes the kinetics of the decomposition of N-Cl-Valine in aqueous solution, which is formed rapidly by chlorination of Valine with sodium hypochlorite. A general-base catalyzed process not yet described is reported. The experimental evidence shows two competitive decomposition paths: an unimolecular concerted fragmentation process (k = (1.8 ± 0.1) · 10^?4 s^?1 at 298 K) and the other one is an E2 elimination process whose importance increases with pH and depends on the nature and the concentration of the bases present in the medium. © 1994 John Wiley & Sons, Inc.     

A study of polarized low-frequency spectra of the solid solution of paradibromobenzene with parachloronitrobenzene in the α phase

Polarized spectra of low-frequency Raman scattering in solid solutions of paradibromobenzene with parachloronitrobenzene in the α phase are studied at temperatures of 293 and 77 K. The solid solution spectrum is found to be similar to the paradibromobenzene spectrum (in accordance with the X-ray diffraction data), but has a series of additional low-intensity lines resulting from disordering. As the parachloronitrobenzene concentration increases, frequencies of the solid solution orientation vibrations decrease steadily, and the half-widths grow. Frequency spectra of the mixed crystal are calculated by the Dean method.     

LIDAR mapping of ozone-episode dynamics in Paris and intercomparison with spot analyzers Supplementary material available at http://link.springer.de/journals/apb

Continuous mapping of an ozone episode in Paris in June 1999 has been performed using a differential absorption lidar system. The 2D ozone concentration vertical maps recorded over 33 h at the Champ de Mars are compiled in a video clip that gives access to local photochemical dynamics with unprecedented precision. The lidar data are compared over the whole period with point monitors located at 0-, 50-, and 300-m altitudes on the Eiffel Tower. Very good agreement is found when spatial resolution, acquisition time, and required concentration accuracy are optimized. Sensitivity to these parameters for successful intercomparison in urban areas is discussed. Received: 11 February 2002 / Published online: 14 March 2002     

Multivalued differential equations on closed convex sets in Banach spaces

New derivation results for integrands and multifunctions via the Lipschitzean approximations are obtained. Applications to multivalued differential equations on closed convex sets are presented.     

The dependence of electron capture rate constants on some molecular parameters

We have analyzed the dependence of the thermal electron capture rate constant on molecular parameters as dipole moment, electronic and orientational polarizabilities. We have found that there is a linear dependence between the logarithm of the rate constant and the electronic polarizability on the electron-accepting center.