Gas-chromatographische Bestimmung des Verhältnisses 2-Methylbutanol (2MB): 3-Methylbutanol (3MB) in verschiedenen Weinbrand- und Whiskysorten

Analytical and Bioanalytical Chemistry -     

Polymers Containing Lactone Groups

Polymers containing intact lactone groups are a new class of macromolecules with reactive groups, which are relatively easy to obtain by polymerization, polycondensation and polyaddition, as well as by reactions on existing macromolecules. Polymers with β-lactone Groups in particular can enter into numerous addition reactions, which can be used, for example, to obtain macromolecules containing hydroxy acid or amino acid groupings. The reactions proceed under mild conditions, and can even be carried out in aqueous media, frequently giving water-soluble polymers. The polymers can be cross-linked at low temperatures, even from the aqueous phase, by the addition of bifunctional or oligofunctional reagents. Polymers containing β-lactone groups can also be used as a basis for graft co-polymers; polyester or polyether branches can be grafted on, depending on whether monomeric lactones or monomeric epoxides are used.     

Synthesis and properties of residual graphite nitrate obtained by treatment of graphite nitrate with water

The possibility of obtaining residual graphite nitrate by water treatment of graphite nitrate and its subsequent drying was studied. The expansion coefficients were determined in the temperature range 500–900°C with a step of 100°C for the samples obtained.     

Méthode de marquage de groupes carboxyliques dans les peptides. Propriétés chromatographiques et autres,de peptide-p,p′-dimapa-anilides

Résumé Les auteurs décrivent une méthode efficate et les conditions (faibles valeurs de pH, milieu dioxane/eau (1∶2), carbodiimide hydrosoluble) de formation de peptides colorés par réaction de leur groupe carboxylique avec un colorant aminé (par exemple: 1(4-diméthylamino-1 phénylazo)-4-aminobenzène=p,p′-dimapa-aniline), sans polymérisation du peptide non-protégé. Quelques méthodes chromatographiques, faciles à mettre en oeuvre, pour l'isolement de peptide-p,p′-dimapa-anilides et quelques propriétés de ces nouveaux composés (peptides-C-colorés) sont présentées.

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Method for labelling carboxylic groups in peptides. Chromatographic and other properties of peptide-p,p′-dimapa-anilides

Summary The authors describe an effective method and the conditions (low pH values, dioxane/water (1∶2) media, watersoluble carbodiimide) for making coloured carboxylic peptides from amino-dye (i.e.: 1(4-dimethylamino-1 phenylazo)-4-aminobenzene=p,p′-dimapa-aniline), without polymerisation of unprotected peptide. Some easy chromatographic methods for isolation of peptide-p,p′-dimapa-anilides and some properties of these new compounds (C-dyed-peptides) are given.

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The collection and determination of atmospheric gaseous bromine and iodine

A procedure has been developed which allows for the isolation, collection and analysis of atmospheric gaseous iodine and bromine. Particulate matter is removed from the airstream to be sampled by electrostatic precipitation. The gaseous halogen species are adsorbed onto specially cleaned activated charcoal. After irradiation of the charcoal sample with thermal neutrons, the iodine and bromine are removed from the charcoal, isolated, and purified as the AgX precipitate. The amounts of gaseous iodine and bromine are then determined by β-counting. The system works well for air sheds with low particulate iodine and bromine concentrations relative to that in the gaseous phase. In air sheds where the particulate halogen predominates, the gas phase measurements are more uncertain.