Polyethylene compounds with antimicrobial surface properties

The present study aims at antimicrobial polyethylene surfaces. To achieve this, LLDPE was compounded with the polymeric biocide poly(2-tert-butylaminoethyl) methacrylate TBAM (bulk modification with 1.5-5.0 wt.% of TBAM). Surfaces of these polymer compounds were then subjected to microbial assays. Using standard methods the colony forming units (CFU) for Escherichia coli and Staphylococcus aureus were determined on these surfaces. In all cases, polyethylene surfaces with highly antimicrobial properties were achieved. An average reduction of 10⁴ CFU ml⁻¹ compared to neat LLDPE was achieved. The surfaces of these LLDPE/TBAM compounds were assessed by electrokinetic (zeta potential) measurements. The results indicate a relation between the antimicrobial activity and the zeta-potential of the polymer compounds. Moreover, the antimicrobial compounds were investigated towards biofilm formation. Compared to pristine LLDPE, the surfaces of the polymer compounds showed less adhering biofilm after a testing period of 16 weeks.     

Conformal field algebras with quantum symmetry from the theory of superselection sectors

According to the theory of superselection sectors of Doplicher, Haag, and Roberts, field operators which make transitions between different superselection sectors—i.e. different irreducible representations of the observable algebra—are to be constructed by adjoining localized endomorphisms to the algebra of local observables. We find the relevant endomorphisms of the chiral algebra of observables in the minimal conformal model with central chargec=1/2 (Ising model). We show by explicit and elementary construction how they determine a representation of the braid groupB which is associated with a Temperley-Lieb-Jones algebra. We recover fusion rules, and compute the quantum dimensions of the superselection sectors. We exhibit a field algebra which is quantum group covariant and acts in the Hilbert space of physical states. It obeys local braid relations in an appropriate weak sense.     

Nachweise verwandter Elemente nebeneinander in einem Tropfen. II. Mitteilung: Der mikrochemische Nachweis von Aluminium und Beryllium mittels Ammoniummolybdats

Zusammenfassung Entgegen den Auffassungen von van Zijp über den von ihm veröffentlichten Nachweis des Aluminiums mit Ammoniummolybdat wurde gezeigt, daß ein derartiger Nachweis Empfindlichkeit und Störungsfreiheit in hohem Grade vereint.Der Nachweis durch Ammoniummolybdat konnte auf Beryllium ausgedehnt werden. Eine Reihe von Versuchen zeigte, daß Aluminium- und Berylliummolybdat in zwei verschiedenen Krystallformen ohne gegenseitige Beeinträchtigung selbst nebeneinander auszukrystallisieren vermögen.Es ist mir eine angenehme Pflicht, Herrn Prof. Dr. Wilhelm Böttger für sein stets färderndes Interesse und für die mikrochemische Arbeitsmäglichkeit überhaupt zu danken. Zu Dank verpflichtet bin ich auch der Fa. Otto Perutz, München für die freundliche überlassung von Pervola-Platten zu den Mikrophotographien.     

MDGC–MS: A powerful tool for enantioselective flavor analysis

This paper reports the differentiation between the enantiomers of theaspiranes and theaspirones, potent flavor compounds widely used in the flavor industry. Optically pure reference compounds of isomeric theaspiranes were obtained by enantioselective synthesis. Enantiomerically pure reference theaspirones were isolated from quince fruit; their absolute stereochemistry was assigned by CD spectroscopy. For both types of compounds the order of elution was elucidated by using authentic reference compounds. These data enabled the determination of the enantiomeric distribution of both types of compounds in a variety of plant tissues. Because of the complexity of the natural flavor isolates, compounds were identified by mass spectrometry after multidimensional gas chromatography employing a Sichromat 2 double oven chromatograph. After separation of the target compounds on the first, achiral, column (DB-5), they were transferred to a chiral column (C-Dex B) for determination of the enantiomeric distribution. Multiple ion detection (MID) enabled the determination of the enantiomeric distribution even for complex mixtures containing the target compounds at extremely low levels.     

Untersuchungen an reagenzien zur photometrischen zinnbestimmung

The formation of complexes between tin(IV) and o-diphenols, and o-hydroxyquinones, has been studied spectrophotometrically. Simple o-hydroxyquinones do not react with tin(IV), chloranilic acid gives an SnR₂ complex, and o-diphenols give SnR₃ complexes. The reactions of tin(IV) with hydroxyxanthene dyes to give coloured products were considered for their possible analytical utility: the pH range, absorption spectrum, solubility and composition of the complexes were investigated, and the stability constants determined. Analytical procedures have been developed for tin and checked for precision and sensitivity: gallein and hydroxyhydroquinonephthalein (dihydroxyfluorescein) are to be recommended.     

Determination of 1-vinyl-2-pyrrolidone in human serum by high-performance liquid chromatography

Summary A simple method is described which allows the quantification of 1-vinyl-2-pyrrolidone (NVP) in human serum. NVP is extracted from serum with diethylether and determined with HPLC/UV-detection. 1-Cyclohexyl-2-pyrrolidone serves as an internal standard. The detection limit is 0.1 mg/l. The method has shown that NVP can enter the organisms of workers occupationally exposed to this substance.     

Zur Theorie der Chiralitätsfunktionen

The Algebraic Theory of Chirality Functions is derived by means of exclusively qualitative considerations. Hence, the significance of quantitative results is questionable. Moreover the construction of “Näherungsansätze” (”Approximation-Ansatz”), which may be interpreted as semiempirical methods, is achieved on the basis of plausibility and mathematical simplicity. Since physical arguments are not included, the consistency or inconsistency of “Näherungsansätze” with experimental results do not justify direct physical conclusions.     

N-heterocyclic carbenes as ligands in high-valent molybdenum and tungsten complexes

Oxometal complexes of molybdenum and tungsten in high oxidation states from stable adducts with 1,3-dimethylimidazoline-2-ylidene (L) 1. The first ‘carbene’ complexes of molybdenum(VI) [MoO₂Cl(L)₃]Cl (3a) and tungsten(VI) WO₂Cl₂(L)₂ (4b) are reported.