Purification of selenoprotein Ph from human plasma

There are three selenium-containing proteins in human plasma: glutathione peroxidase (GSH-Px-P), albumin and selenoprotein Ph, the human analogue to selenoprotein P from rat plasma. Selenoprotein Ph was separated from the two other selenium-containing proteins by Heparin Sepharose chromatography and was shown to have about 60-70% of the total plasma selenium, while both GSH-Px-P and albumin contain about 15%. A 2588-fold purification from human plasma was achieved by using a four-step procedure. SDS-PAGE of the purified selenoprotein revealed, besides one contaminant selenium-free protein band at about 70 kDa, one selenium-containing band ranging from 54 to 67 kDa with a maximum at 63 kDa. This microheterogeneity, also recognized by IEF, may be due to the glycprotein nature of the selenoprotein Ph. The determination of the molecular mass of the native protein varied from 65 kDa using gel filtration on Fraktogel HW 55 to 89 kDa on Sephacryl S-200 HR, suggesting an interaction between the gel-matrices and selenoprotein Ph.     

Epoxidizable Fatty Amide–Phenol Conjugates

This paper reports the synthesis of a series of novel compounds where carboxylic acids have been linked to a phenol through amidomethyl units. For instance, one, two, or three fatty acids have been selectively appended to the phenol in yields above 75%. The fatty acid used was oleic acid, which was subsequently epoxidized. Other functional groups, such as amino acids, can be incorporated in these compounds. Examples of monomers that are suitable for polymerization were also prepared: one acrylamide, one styrene derivative, and two types of AB₂ diamino acids, all of which contain oleic units that are sites for epoxidation and crosslinking. Fatty acid aryl ethers were prepared using hydroxy fatty acids. These molecules are intended to serve as augmented analogues of epoxidized vegetable oil. Their amide groups should lead to intermolecular aggregation through hydrogen bonding, and the option to covalently include other functional groups may permit tuning of the macroscopic materials properties of films, coatings, or solids constructed from them.     

n-Type Doping of Vapor–Liquid–Solid Grown GaAs Nanowires

In this letter, n-type doping of GaAs nanowires grown by metal–organic vapor phase epitaxy in the vapor–liquid–solid growth mode on (111)B GaAs substrates is reported. A low growth temperature of 400°C is adjusted in order to exclude shell growth. The impact of doping precursors on the morphology of GaAs nanowires was investigated. Tetraethyl tin as doping precursor enables heavily n-type doped GaAs nanowires in a relatively small process window while no doping effect could be found for ditertiarybutylsilane. Electrical measurements carried out on single nanowires reveal an axially non-uniform doping profile. Within a number of wires from the same run, the donor concentrations N _D of GaAs nanowires are found to vary from 7 × 10¹⁷ cm^-3 to 2 × 10¹⁸ cm^-3. The n-type conductivity is proven by the transfer characteristics of fabricated nanowire metal–insulator-semiconductor field-effect transistor devices.     

Development of a 100 W rechargeable bipolar zinc/oxygen battery

A bipolar filter press-type electrically rechargeable Zn/O2 battery has been developed. Reticulated copper foam served as substrate for the zinc deposit on the anodic side, and La0.6Ca0.4CoO3-catalysed bifunctional oxygen electrodes were used on the cathodic side of the cells. The 100cm2 unit cell had an open circuit voltage of 1.4V (O2) in moderately alkaline electrolyte. The open circuit voltage and the peak power measured for a stack containing seven cells were sim 10V and sim 90W, respectively. The current-potential behaviour was determined as a function of the number of bipolar cells, and the maximum discharge capacity was determined at different discharge rates.     

Photo‐induced Charge Transfer and Relaxation of Persistent Charge Carriers in Polymer/Nanocrystal Composites for Applications in Hybrid Solar Cells

The photo‐induced charge transfer and the dynamics of persistent charge carriers in blends of semiconducting polymers and nanocrystals are investigated. Regioregular poly(3‐hexylthiophene) (P3HT) is used as the electron donor material, while the acceptor moiety is established by CdSe nanocrystals (nc‐CdSe) prepared via colloidal synthesis. As a reference system, organic blends of P3HT and [6,6]‐phenyl C₆₁‐butyric acid methyl ester (PCBM) are studied as well. The light‐induced charge transfer between P3HT and the acceptor materials is studied by photoluminescence (PL), photo‐induced absorption (PIA) and light‐induced electron spin resonance spectroscopy (LESR). Compared to neat P3HT samples, both systems show an intensified formation of polarons in the polymer upon photo‐excitation, pointing out successful separation of photogenerated charge carriers. Additionally, relaxation of the persistent charge carriers is investigated, and significant differences are found between the hybrid composite and the purely organic system. While relaxation, reflected in the transient signal decay of the polaron signal, is fast in the organic system, the hybrid blends exhibit long‐term persistence. The appearance of a second, slow recombination channel indicates the existence of deep trap states in the hybrid system, which leads to the capture of a large fraction of charge carriers. A change of polymer conformation due to the presence of nc‐CdSe is revealed by low temperature LESR measurements and microwave saturation techniques. The impact of the different recombination behavior on the photovoltaic efficiency of both systems is discussed.     

Parallel FTIR-ATR and gravimetrical in-situ measurements on sodium alanate powder samples during hydrogen desorption

An experimental set-up has been developed to carry out in-situ measurements on hydrogen storage materials. It has been used to perform FTIR–ATR measurements on sodium alanate samples during hydrogen desorption and, in parallel, to perform gravimetrical measurements on the same sample. The ATR spectra showed the typical broad Al–H vibrational features, changing according to the phase change the material undergoes during the load cycle. It is shown that the absorbance of the material at these bands and the hydrogen content correspond to each other in a reproducible way. This behavior may be used to measure the hydrogen mass released by an alanate hydrogen reservoir by measuring the optical absorbance at defined wavelengths. In this paper the results of these experiments that may give rise to the realization of a level sensor in future hydrogen storage applications are presented.     

Origin of Gas Porosity in Gold-Based Alloys Cast in Calcium Sulfate-Bonded Investment and Influence of Metal Oxide Acid–Base Properties on Calcium Sulfate Thermal Stability

The origin of gas-porosity in gold-based alloys produced via lost-wax casting in CaSO₄-bonded investment has been identified using a combination of microanalytical and thermal techniques. The occurrence of gas-porosity is related to the thermal decomposition of CaSO₄, which, with SiO₂, constitutes the investment material and decomposes at a temperature very close to the casting temperature of some typical gold alloys used for jewelry production. The thermal reaction generates SO₂, leading to gas-porosity and, therefore, to defective products. Furthermore, the results show the detrimental effect of thermal decomposition caused by the presence of ZnO, Cu₂O, CuO, NiO, and Ag₂O formed on the surface of the gold-based alloy during air melting or casting. Therefore, the solid-state thermal decomposition of CaSO₄ in the presence of other ceramic oxides has been investigated and found to be related to their surface acid–base properties, measured as isoelectric points on the solid surface.     

SOCIO-ECONOMIC ASPECTS OF THE AUSTRIAN 200 kWp-PHOTOVOLTAIC-ROOFTOP PROGRAMME

Between 1992 and 1994 a 200 kWp-rooftop programme to promote small grid-connected Photovoltaic (PV) systems was conducted in Austria. Within this programme about 100 PV systems with an average capacity of 2.28 kWp were installed. This paper investigates the socio-economic aspects of this programme and the prospects for a further dissemination of this technology. The major conclusions of this investigation are as follows: (1) The motives to invest in a PV system are: (i) environmental protection; (ii) an alternative to nuclear power; (iii) technical interest. Yet, it is also important that the public supports this purchase by means providing subsidies. (2) The purchase of a PV system leads to different changes in consumer behaviour. Consumers with low initial consumption increased their electricity demand slightly, while the majority of consumers with high initial electricity demand saved electricity. (3) The financial incentives in the programme were not optimally designed. With the same amount of total subsidies it would have been possible to promote more PV systems. (4) The key factors for a further dissemination of PV systems are: (i) financial incentives; (ii) a reduction of the investment costs; (iii) increase in reliability; (iv) distribution of information; (v) enhancement of environmental awareness.