Classification of wine distillates using multivariate statistical methods based on their direct GC-MS analysis

This work describes a novel methodology for the recognition of brandies based on direct injection of a raw sample followed by GC-MS analysis. Direct injection was chosen for its simplicity and the fact that the composition of the samples analysed remains unchanged compared to original brandy. The repeatability of the analytical procedure was evaluated by a comparison of the peak areas for randomly selected compounds obtained from 10 parallel measurements. A novel chemometric procedure was investigated in order to separate the samples studied on the basis of their geographical origin, processing technology or maturation time. In this procedure, a principal component analysis was applied to full chromatograms to select the time interval that shows the significant differences between the samples studied. It was shown that the chromatogram recorded at 36–39 min bore the maximal differences, hence it could be used to classify the brandy samples. The chromatographic peaks found within this time interval were identified and their peak areas determined. These compounds could be used as specific markers for determining geographical origin or processing technology.     

Deep oxidative desulfurization of benzothiophene and dibenzothiophene with a peroxophosphotungstate–ionic liquid brush assembly

A novel, efficient and reusable heterogeneous catalytic assembly of peroxophosphotungstate held in an ionic liquid brush was synthesized and an extraction and catalytic oxidative desulfurization (ECODS) procedure was developed for a model oil of benzothiophene (BT) and dibenzothiophene (DBT) using 30 wt% hydrogen peroxide as terminal oxidant and methanol as solvent under mild conditions. Several factors that affect sulfur removal were investigated in detail. The highest sulfur removal can reach 100% for BT in 7 h at 70 °C when the molar ratio of H₂O₂, S and catalyst is 10:1:0.025. The sulfur removal for DBT can also reach 100% in 4 h at 50 °C with the same molar ratio of H₂O₂, S and catalyst. The experimental results demonstrate that this ECODS process has no apparent scale‐up effect. The catalyst can be easily recovered (via simple filtration) and recycled five times without a significant decrease in activity. Copyright © 2015 John Wiley & Sons, Ltd.     

Small orthomodular partial algebras

Orthomodular partial algebras (OMAs) can be seen as the algebraic representation of orthomodular posets. We use Greechie diagrams for the graphical representation of OMAs and investigate characterizations for the strong embeddability of a given OMA into a Boolean OMA. We present a complete list of the Greechie diagrams of OMAs up to 24 elements, and we show that there exists an infinite OMA that is generated by 4 elements.     

Palladium-Catalyzed Direct C2-and Further C7-Acylation of Indoles with Aldehydes

The palladium‐catalyzed direct C2‐ and further C7‐acylation of indoles with aldehydes have been developed. This method provides a convenient pathway toward a variety of mono‐ and diacylated indoles.