An investigation into the ultrasonic treatment of polluted solids

Granular pieces of brick impregnated with copper oxide were used as a model for contaminated soil. Washing this model substrate by passing water across the substrate on an ultrasonically shaken tray irradiation afforded a 40% reduction in copper content. This was compared with only a 6% reduction when the sample was treated under otherwise identical conditions but using a tray shaken conventionally. The majority of the copper was removed as a result of the removal of surface materials which were more heavily contaminated with the copper oxide.     

1′‐Acetyl­ferrocene‐1‐carboxyl­ic acid: an instance of hydrogen bonding in the rare dimeric acid‐to‐ketone mode

The title compound, [Fe(C₆H₅O₂)(C₇H₇O)], adopts a conformation involving partial staggering of its rings and aggregates in the solid as acid‐to‐ketone hydrogen‐bonding dimers [O?O = 2.720 (4) Å and O—H?O = 164°] having centro­symmetrically related components. Close intermolecular C—H?O contacts were found to both carboxyl O atoms.     

Achieving traceable chemical measurements: inter-laboratory evaluation of a simplified technique for isotope dilution mass spectrometry. Part 2. Methodology for high accuracy analysis of organic analytes

A high accuracy measurement procedure developed and validated at LGC has been transferred to a number of expert UK laboratories, and their experience in applying the technique has been evaluated by inter-laboratory comparisons. It is an “exact matching” calibration procedure for analysis of organic analytes using isotope dilution mass spectrometry (IDMS). This calibration procedure uses a calibration blend and a sample blend with closely matched isotope amount ratios, and is an iterative process, culminating in the calibration blend and sample blend having identical isotope amount ratios. It is capable of high accuracy, since systematic errors in the determination of the isotope amount ratios are cancelled out. A series of four inter-laboratory comparisons of increasing difficulty were carried out involving a number of expert laboratories. The first three comparisons used gas chromatography mass spectrometry (GC–MS) analysis of the pesticide metabolite (pp′-dichlorodiphenyl) dichloroethylene (pp′-DDE), involving both conventional calibration and IDMS exact matching procedures for pp′-DDE in a solvent and a complex liquid matrix (corn oil). The fourth comparisons utilised liquid chromatography mass spectrometry (LC–MS) and involved the analysis of sulphamethazine (4-amino-N-(4,6 dimethyl-2 pyrimidinyl) benzenesulphonamide) in solvent using IDMS and conventional calibration techniques. Following the first trial, a workshop for participants was held on the use of the exact matching procedure together with a short course on uncertainty estimation. The results of the comparisons clearly showed the superior accuracy of using IDMS with the exact matching procedure for both GC–MS and LC–MS applications. These comparisons and the workshop have enabled the methodology to be transferred to UK industry, helping to improve UK measurement capability.

     

trans‐4‐Acetylcyclo­hexane­carboxyl­ic acid and ()‐trans‐2‐acetyl­cyclo­hexane­carboxyl­ic acid: hydrogen‐bonding patterns in two isomeric keto acids

Both title compounds, C₉H₁₄O₃, display carboxyl‐dimer hydrogen‐bonding patterns. The 4‐acetyl isomer adopts a chiral conformation with negligible disordering of the methyl and carboxyl groups and forms centrosymmetric dimers across the b and c edges of the chosen cell [O?O = 2.667 (3) Å and O—H?O = 175°]. Intermolecular C—H?O close contacts were found for both carbonyl groups. In the 2‐acetyl isomer, there is no intramolecular interaction between the carboxyl and acetyl groups and the hydrogen bonding involves centrosymmetric carboxyl dimerization across the ab and ac faces of the chosen cell [O?O = 2.668 (2) Å and O—H?O = 173°]. The carboxyl group is negligibly disordered, but significant rotational disordering was found for the acetyl methyl group. An intermolecular C—H?O close contact was found involving the ketone group.     

Ketone enolization with lithium dialkylamides: the effects of structure,solvation, and mixed aggregates with excess butyllithium

The effects of lithium dialkylamide structure, mixed aggregate formation, and solvation on the stereoselectivity of ketone enolization were examined. Of the lithium dialkylamides examined, lithium tetramethylpiperidide (LiTMP) in THF resulted in the best enolization selectivity. The stereoselectivity was further improved in the presence of a LiTMP-butyllithium mixed aggregate. The use of less polar solvents reduced the enolization stereoselectivity. Ab initio calculations predict LDA and LiTMP to form mixed cyclic dimers in ethereal solvents. The calculations also predict LiTMP-alkyllithium mixed aggregates to competitively inhibit the formation of less stereoselective LiTMP-lithium enolate mixed aggregates.     

Effects of nonequilibrium on velocity and plate height in reactive capillary electrophoresis

Models for velocity and plate height for reactive CE are developed under the formalism of generalized nonequilibrium theory, as described by Giddings. The resultant equations are consistent with chromatographic theory and validated with an independent stochastic simulation. Moreover, unlike prior methods for CE, this model allows calculation of thermodynamic equilibrium constants and kinetic rate constants from a single, undistorted peak. The theoretical development shows that velocity is directly dependent on the equilibrium constant and is independent of the rate constant. On the other hand, plate height varies little with equilibrium constant and is inversely proportional to rate constant. The ability to evaluate equilibrium constants from velocity and rate constants from plate height is most greatly influenced by electric field strength and mobility difference. The accuracy in calculated equilibrium constants is limited by mobility difference; however, the accuracy in rate constants is limited by plate height and equilibrium constant.     

Potentiometric finish in the Schöniger Halogen Method

Summary Modifications for a potentiometric finish to the oxygen flask halogen method are given. Results show its reliability for routine determinations.

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Zusammenfassung Die potentiometrische Endbestimmung der Halogene nach der Flaschen-methode vonSchöniger wird beschrieben. Die Ergebnisse zeigen die Anwendbarkeit für Routineanalysen.

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Résumé On apporte des modifications à la méthode de dosage des halogènes par la fiole à oxygène, pour terminer potentiométriquement. Les résultats montrent que l'on peut l'appliquer aux dosages en série.