An algebraic characterization of vacuum states in Minkowski space

An algebraic characterization of vacuum states on nets ofC ^*-algebras over Minkowski space is given and space-time translations are reconstructed with the help of the modular structures associated with such states. The result suggests that a condition of geometrical modular action might hold in quantum field theories on a wider class of spacetime manifolds.     

High Frequency Dielectric Relaxation of a Ferroelectric Liquid Crystal

Dielectric relaxation measurements on a optically active thiadiazole derivative in the frequency range from 1 MHz to 1 GHz gave relaxation frequencies between 100 MHz and 1 GHz in the smectic C* phase. This relaxation which is related to molecular reorientation processes around the long molecular axis is connected with a mean activation energy of 57 kJmol⁻¹. A simple model of the energetic behaviour of this reorientation including the production of the spontaneous polarization is discussed.     

The effect of iron on the precipitation in an Al-Mg-Si alloy

The effect of iron on the precipitation of a technical Al-Mg-Si alloy was studied by macroand microhardness, Y-modulus and SANS with DKD and was compared with a pure alloy. The iron phases of the technical alloy were preferentially considered by the SANS. In addition the damping by the elastomat of FÖRSTER and the variance of the microhardness were measured. It was found that iron essentially influences the kinetics of the precipitate, particularly the mechanism of nucleation and precipitation sequence.     

Product states for local algebras

Let ()() and () () be the von Neumann algebras associated with the space-tiem regions and respectively in the vacuum representation of the free neutral massive scalar field. For suitably chosen spacelike separated regions and it is proved that there exists a normal product state of (), Some consequences for the algebraic structure of the local rings are pointed out.     

Suitability of hyperbranched polyester for sensoric applications – investigation with reflectometric interference spectroscopy

Hyperbranched polyesters (HBP) with different end groups (P-OH, P-COOH, P-OAc) were prepared as thin films. Their surface properties were investigated using zeta potential and contact angle measurements. The differences in surface properties between P-OH and P-COOH, on the one hand, and P-OAc, on the other hand, predicted different behavior in sensoric applications. Therefore, the vapor of the homologous series of alcohols from methanol to pentanol was exposed to the thin films. Changes in thickness were observed with reflectometric interference spectroscopy (RIfS). First investigations in a current analytical problem for the detection and discrimination of refrigerants (freons) using P-OH as sensitive layer have been shown. Polydimethylsiloxane (PDMS) and poly(ether urethane) (PUT) were used as reference sensor materials for the RIfS measurements.     

Shallow-underground accelerator sites for nuclear astrophysics: Is the background low enough?

In order to reliably estimate the rate of a charged particle induced nuclear reaction in a non-explosive astrophysical scenario, its cross-section must be measured far below the Coulomb barrier. However, at the corresponding energies the cross-section values are very low, so that the experimental counting rate is dominated by cosmic-ray induced background, even if a suitable anticoincidence shield is applied. This problem can be overcome by performing an accelerator-based experiment in a deep underground site, as has been done with great success at the LUNA 0.4MV accelerator in Gran Sasso, Italy. Several underground accelerators with higher beam energy are in the planning phase worldwide. All of them are shielded by over 1000m of rock, a depth at which cosmic-ray effects are negligible for the purposes of nuclear astrophysics experiments. It is shown here that a combined approach, using a shallow-underground laboratory below 47m of rock and an active shield to veto surviving muons in simple detectors, results in a background level that is not far from that of deep underground sites. Data have been obtained using two ??traveling?? ??-detectors. They have been transported both shallow underground, to the Dresden Felsenkeller in Germany, and deep underground, to the Gran Sasso laboratory in Italy. As shallow-underground facilities are more easily accessible than deep-underground ones, the present finding holds the promise of greatly accelerated progress in the field of cross-section measurements for nuclear astrophysics.     

A new weakly basic amino‐reactive fluorescent label for use in isoelectric focusing and chip electrophoresis

In this study, we present a novel amino‐reactive fluorescence marker (referred to as UR‐431), which is well suited for electrophoretic techniques. A main feature of this marker is its weakly basic behavior when conjugated to analytes. Labeled primary amines exhibit a positive net charge and accordingly a cathodic mobility below a pH of 2.4. The label features a pH‐independent fluorescence emission and is thus very interesting for electrophoretic applications such as IEF. The absorption maximum of this yellow daylight chromophore is at 431 nm, whereas fluorescence emission peaks at 537 nm (quantum yield≈0.1). The label was successfully conjugated to amines, peptides and proteins and separated via CE and MCE. The on‐chip detection limit of labeled lysine using a mercury‐lamp‐based fluorescence microscope was determined as 12 nM. An important feature of the new label is that it effects only a subtle change of the pI of proteins compared with common anionic labels, e.g. FITC. pI values of proteins were investigated by comparing native proteins and labeled proteins in CIEF. UR‐431 was also applied to sensitive detection of amines and peptides in MCE.     

Evaluation of solid adsorbent materials for cryogen-free trapping-gas chromatographic analysis of atmospheric C2-C6 non-methane hydrocarbons

Nine commercial solid adsorbent materials (in order of decreasing surface area: Carboxen 1000, Carbosieve S III, molecular sieve 5A, molecular sieve 4A, silica gel, Carboxen 563, activated alumina, Carbotrap and Carboxen 1016) were investigated for their ability to trap and release C2-C6 non-methane hydrocarbons (NMHCs) in atmospheric samples for subsequent thermal desorption gas chromatography-flame ionization detection analysis (GC-FID). Recovery rates for 23 NMHCs and methyl chloride (CH3Cl) were determined. A microtrap filled with the three adsorbents Carbosieve S III, Carboxen 563 and Carboxen 1016 was found to allow for the analysis of the widest range of target analytes. A detection limit of approximately 3pptC [parts per trillion (carbon)] in a 1l air sample and a linear response over a wide range of volatilities and sample volumes was determined for this configuration. Water vapor in the sample air was found to causes interference in trapping and subsequent chromatographic analysis of light NMHCs. A Peltier-cooled, regenerable water trap inserted into the sample flow path was found to mitigate these problems and to allow quantitative and reproducible results for all analytes at all tested humidity conditions.