Continuous solid-phase extraction and preconcentration of bisphenol A in aqueous samples using molecularly imprinted columns

A bisphenol A (BPA) molecularly imprinted polymer, the composition of which was optimised using a chemometric approach, has been applied to the selective preconcentration of the template from aqueous samples. The selectivity of the polymer toward BPA and related compounds was evaluated chromatographically. The BPA-imprinted polymer was packed in a column and used for continuous on-column solid-phase extraction (MISPE) of aqueous samples followed by subsequent analysis by HPLC with fluorescence detection of the eluted fractions. The composition of the washing solvent applied in the MISPE procedure was optimised to favour the specific interactions of the MIP with BPA and to remove the non-selectively bound matrix components. The MISPE method has proven to be effective for selective preconcentration of BPA in aqueous samples (recoveries >84% obtained in the eluate for 10–100 mL sample volumes) enabling detection and quantification limits of 1.0 and 3.3 ng mL^–1, respectively (based on 25 mL sample size). Analytical recoveries were between 92 and 101% for river water samples spiked with known amounts of BPA (30, 60, and 80 ng mL^–1); relative standard deviations (RSD) were lower than 5.0%.     

16, 18O induced transfer reactions on122, 120Sn

The reactions¹²⁰Sn+72 MeV¹⁸O and¹²²Sn+74 MeV¹⁶O were investigated with time of-flightE-E-telescopes. Data are presented for all quasi-elastic reaction channels. The two neutron stripping and pickup reactions (¹⁸O,¹⁶O), (¹⁸O,²⁰O) and (¹⁶O,¹⁸O) are analyzed in detail. It is shown that these heavy ion induced two neutron transfer reactions proceed with essentially the same type of selectivity as the corresponding light ion induced reactions. The differential cross sections for transfer reactions leaving the^{120, 122}Sn nuclei in their 2⁺ first excited states are shown to be influenced by interference effects due to additional inelastic excitations.     

Inner-shell ionization ofZ=25–32 elements by 5-48 MeV32S ions

TheK-shell ionization cross sections of Mn, Ni, Cu, Zn and Ge under³²S bombardment have been measured in the energy range from 5 to 48 MeV. The cross sections are compared with available theories based on a direct Coulomb ionization mechanism and with the predictions of theK-vacancy sharing process. This last process can reasonably account for the measured cross sections at high bombarding energies. The energy shifts of theK - andK -lines and theK /K -intensity ratios have also been measured. This information is used to deduce the defect configuration of the atoms. The mechanisms responsible for the multiple vacancy production are discussed.     

A one step synthesis of novel 4-alkoxy-β-lactams by high pressure promoted [2 + 21 cycloadditions of enol ethers and isocyanates derived from amino acids

Abstract

Novel moni-β-lactams derived from esters of amino acids have been prepared in one step by the high pressure promoted [2 + 2] cycloaddition of enol ethers with isocyanates derived from esters of amino acids. The effect of substituents in the enol ether and in the isocyanate on the scope of the synthesis has been demonstrated.     

Elimination of the type B uncertainty

An uncertainty of an estimated parameter can be, in general, decomposed into two parts, i.e. an uncertainty caused by errors in the actual experiment (the type A uncertainty) and an uncertainty caused by errors in preceding experiment, where some wanted constants were estimated (the type B uncertainty). These constants are necessary for an estimation of the useful parameters. The aim of the paper is to find a condition for elimination of the type B uncertainty.     

Concentration variations in the optical pseudogap and refractive index of crystals of Cu6PS5I1–xClx solid solutions

The effect of anionic substitution of halogen atoms on the spectral position and shape of the optical absorption edge and the dispersion of the refractive index of crystals of Cu₆PS₅I_1–xCl_x solid solutions are studied. The concentration dependences of the width of the optical pseudogap, refractive index, and lattice parameters are shown to be interrelated in these solid solution crystals.