Fission fragment mass yields of Th to Rf even-even nuclei

Fission properties of the actinide nuclei are deduced from theoretical analysis. We investigate potential energy surfaces and fission barriers and predict the fission fragment mass yields of actinide isotopes. The results are compared with experimental data where available. The calculations were performed in the macroscopic-microscopic approximation with the Lublin-Strasbourg Drop (LSD) for the macroscopic part, and the microscopic energy corrections were evaluated in the Yukawa-folded potential. The Fourier nuclear shape parametrization is used to describe the nuclear shape, including the non-axial degree of freedom. The fission fragment mass yields of the nuclei considered are evaluated within a 3D collective model using the Born-Oppenheimer approximation.     

Quantifying entanglement of two-qubit Werner states

In this article, we introduce a framework for entanglement quantification of photon pairs represented by two-qubit Werner states. The measurement scheme is based on the symmetric informationally complete POVM. To make the framework realistic, we impose the Poisson noise on the measured two-photon coincidences. For various settings, numerical simulations were performed to evaluate the efficiency of the framework.     

High-speed wavelength-division multiplexing quantum key distribution system

A high-speed quantum key distribution system was developed with the wavelength-division multiplexing (WDM) technique and dedicated key distillation hardware engines. Two interferometers for encoding and decoding are shared over eight wavelengths to reduce the system's size, cost, and control complexity. The key distillation engines can process a huge amount of data from the WDM channels by using a 1 Mbit block in real time. We demonstrated a three-channel WDM system that simultaneously uses avalanche photodiodes and superconducting single-photon detectors. We achieved 12 h continuous key generation with a secure key rate of 208 kilobits per second through a 45 km field fiber with 14.5 dB loss.     

Comparison of ultrasonic degradation rates constants of methylene blue at 22.8 kHz, 127 kHz, and 490 kHz

Techniques such as solvent extraction, incineration, chemical dehalogenation, and biodegradation have been investigated for the degradation of hazardous organic compounds. We found ultrasound to be an attractive technology for the degradation of hazardous organic compounds in water. However, the effects of ultrasonic frequency on degradation rate constants were not investigated quantitatively. In this study, the degradation process of a model for hazardous organic compound methylene blue was investigated using ultrasonic irradiation. The study focused on the effects of ultrasonic frequency and ultrasonic power on the degradation rate constant. The apparent degradation rate constants were estimated based on time dependence of methylene blue concentration assuming pseudo-first-order kinetics for the decomposition. A linear relationship between the apparent degradation rate constant and ultrasonic power was identified. In addition, the apparent degradation rate constants at frequencies of 127 and 490 kHz were much larger than those at 22.8 kHz. A relationship between the apparent degradation rate constant and the sonochemical efficiency value (SE value) was also found. Based on these results, a simple model for estimating the apparent degradation rate constant of methylene blue based on the ultrasonic power and the SE value is proposed in this study.     

Fragrance release profile from sonochemically prepared protein microsphere containers

Protein microspheres have been prepared by sonicating a mixture of pure fragrant oil (amyl acetate (AA)) with an aqueous protein (bovine serum albumin) solution. The prepared protein spheres are nano- to micrometer sized with an encapsulation efficiency of approx. 97% for the AA present on the surface and inside the BSA capsule. Containers were found stable for more than 6 months when stored sealed at 4 °C and 20 °C. For the release profile measurements, we used a simple, automated and direct method. We continuously weighed the encapsulated microspheres and measured the evaporation rates. The release profiles at 15 °C and 25 °C display two different evaporation rates. The higher rate is the sum of a few evaporation rates, including water molecules, while the slower rate is due to the evaporation of pure AA. The changes in the evaporation rates occur upon the collapse of the container. This event coincides with the full evaporation of water. For morphological characterization we dyed the AA with Nile red, and used SEM, ESEM, Cryo-SEM, light microscopy, and confocal laser scanning microscopy measurements.     

Hydrolysis of Cutin by PET-Hydrolases

Functionalisation of synthetic polymers by using enzymes has been recently demonstrated. The major advantage of enzymes over chemical processes lies in their surface specific and endo-wise mode of action. Surface hydrophilisation of PET with lipases and cutinases leads to a dramatic increase of the surfacial acid and hydroxyl group content while conventional chemical treatment does not cause any change. However, this PET-hydrolysing activity by enzymes from distinct classes has not yet been correlated to activity on natural polyesters. Here, we show that lipases, cutinases and a PHA-depolymerase are all capable of hydrolysing PET, while only lipases and cutinases also hydrolysed cutin to various degrees. Lipases showed a higher specificity for terminal fatty acids while the cutinases preferred hydroxy fatty acids during cutin hydrolysis.     

Beiträge zur Lumineszenzanalyse II

Ohne ZusammenfassungI.: Monatsh. Chem.55, 1930, S. 158, bzw. Sitzb. Ak. Wiss. Wien (II b)139, 1930, S. 74.