The Characteristics Study of Helium-Xenon Mixture in Closed Brayton Cycle for Space Nuclear Reactor Power

Differing from the adoption of helium as working fluid of closed Brayton cycle (CBC) for terrestrial high temperature gas cooled reactor (HTGR) power plants, helium-xenon mixture with a proper molar weight was recommended as working fluid for space nuclear reactor power with CBC conversion. It is essential to figure out how the component of helium-xenon mixture affects the net system efficiency, in order to provide reference for the selection of appropriate cycle working fluid. After a discussion of the physical properties of different helium-xenon mixtures, the related physical properties are studied to analyze their affection on the key parameters of CBC, including adiabatic coefficient, recuperator effectiveness and normalized pressure loss coefficient. Then the comprehensive thermodynamics of CBC net system efficiency is studied in detail considering different helium-xenon mixtures. The physical properties study reveals that at 0.7 MPa and 400 K, the adiabatic coefficient of helium-xenon mixture increases with increased molar weight, from 0.400 (pure helium) to 0.414 (pure xenon), while recuperator effectiveness firstly increases and then decreases with the increase of molar weight, and the normalized pressure loss coefficient increases monotonically with molar weight increases. The thermodynamic analysis results show that the adiabatic coefficient has less effect on the net system efficiency, while the net system efficiency increases with increased recuperator effectiveness, and the net system efficiency decreases with normalized pressure loss coefficient increases. Finally, the mixture of helium-8.6% xenon was adopted as working fluid, instead of pure helium, for ensuring less turbine mechanicals (turbine and compressor) stages, and resulting maximum recuperator effectiveness. At the given cold / hot side temperature of 400 / 1300 K, the net system efficiency can reach 29.18% theoretically.

Synthesis and characterization of dextran-coated iron oxide nanoparticles

Synthesis and characterization of iron oxide nanoparticles coated with a large molar weight dextran for environmental applications are reported. The first experiments involved the synthesis of iron oxide nanoparticles which were coated with dextran at different concentrations. The synthesis was performed by a co-precipitation technique, while the coating of iron oxide nanoparticles was carried out in solution. The obtained nanoparticles were characterized by using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction spectrometry, Fourier transform infrared spectroscopy and superconducting quantum interference device magnetometry. The results demonstrated a successful coating of iron oxide nanoparticles with large molar weight dextran, of which agglomeration tendency depended on the amount of dextran in the coating solution. SEM and TEM observations have shown that the iron oxide nanoparticles are of about 7 nm in size.

CORP: The assessment of total hemoglobin mass by carbon monoxide rebreathing

In this Cores of Reproducibility in Physiology (CORP) article, we present the theory and practical aspects of the carbon monoxide (CO) rebreathing method for the determination of total hemoglobin mass in humans. With CO rebreathing, a small quantity of CO is diluted in O2and rebreathed for a specified time period, during which most of the CO is absorbed and bound to circulating hemoglobin. The dilution principle then allows calculation of the total number of circulating hemoglobin molecules based on the number of absorbed CO molecules and the resulting changes in the fraction of carboxyhemoglobin in blood. Total hemoglobin mass is derived by multiplication with the molar weight of hemoglobin. CO rebreathing has been used for >100 yr and has undergone steady improvement so that today excellent values in terms of accuracy and precision can be achieved if the methodological precautions are carefully followed.

Small-angle X-ray scattering and light scattering study of hybrid nanoparticles composed of thermoresponsive triblock copolymer F127 and thermoresponsive statistical polyoxazolines with hydrophobic moieties

A combination of new thermoresponsive statistical polyoxazolines, poly[(2-butyl-2-oxazoline)-stat-(2-isopropyl-2-oxazoline)] [pBuOx-co-piPrOx], with different hydrophobic moieties and F127 surfactant as a template system for the creation of thermosensitive nanoparticles for radionuclide delivery has recently been tested [Pánek, Filippov, Hrubý, Rabyk, Bogomolova, Kučka & Stěpánek (2012).Macromol. Rapid Commun.33, 1683–1689]. It was shown that the presence of the thermosensitive F127 triblock copolymer in solution reduces nanoparticle size and polydispersity. This article focuses on a determination of the internal structure and solution properties of the nanoparticles in the temperature range from 288 to 312 K. Here, it is demonstrated that below the cloud point temperature (CPT) the polyoxazolines and F127 form complexes that co-exist in solution with single F127 molecules and large aggregates. When the temperature is raised above the CPT, nanoparticles composed of polyoxazolines and F127 are predominant in solution. These nanoparticles could be described by a spherical shell model. It was found that the molar weight and hydrophobicity of the polymer do not influence the size of the outer radius and only slightly change the inner radius of the nanoparticles. At the same time, molar weight and hydrophobicity did affect the process of nanoparticle formation. In conclusion, poly(2-oxazoline) molecules are fully incorporated inside of F127 micelles, and this result is very promising for the successful application of such systems in radionuclide delivery.

Synthesis of Diblocks Copolymers PCL-b-PLLA and Optimization of its Mechanical Characteristics

<p>Biodegradable polymeric materials have a wide application in medicine, ecology and a number of other branches of industry. Overwhelming majority of such polymers is well exposed to the biodegradation, but they have mechanical properties which don’t correspond to the requirements of application areas. As a rule, these materials possess low elasticity. In this work, optimization of mechanical properties of biodegradable polymers and the search of structure of block polymer on the basis of ε-caprolactone and L-lactide with the maximal elasticity are considered. The purpose of the work is to receive the diblock polymer with mechanical properties as close as possible to elastomer for medical devices. The task is reached due to application of design of experiment with the subsequent optimization of the received results. Maximization of elongation at maximum load of received polymer is solved by the greatest possible reduction of crystallinity with a variation of molar weight of both part of diblock: polycaprolactone and polylactide. The absolute maximum of elongation at maximum load of synthesized diblock polymers is found. It is established that diblock with the following structure possesses the best mechanical properties in this class of polymers. Molar weight of the polycaprolactone block is 5000 Da while polylactide block is 7000 Da. Elongation at maximum load of this polymer was about 30%. In the second stage of our research, we try to improve the mechanical properties by making one block partly random (PCL-co-PLLA). Second block was made from homopolymer (PLLA). Maximum received elongation at break is 200%. First block of this polymer contains 25% of lactide, has molar weight of 10000 Da. Second block is the pure polylactide, with molar weight 10000 Da. All the experimental results and mathematical modeling pointing direction to maximum elongation could be achieved by multi-block structures.</p>