Národní úložiště šedé literatury Nalezeno 32 záznamů.  předchozí11 - 20dalšíkonec  přejít na záznam: Hledání trvalo 0.01 vteřin. 
HYDROGENATION PROPERTIES OF Mg-Al-Ti-Zr-C COMPOSITE
Král, Lubomír ; Čermák, Jiří ; Roupcová, Pavla
The improvement of hydrogen storage properties of ball-milled Mg-Al-Ti-Zr-C composite was studied in this\npaper. It has been previously shown, that the addition of Ti, Zr, Al and C improves storage properties of Mg.\nThis beneficial effect of additives upon hydrogen storage properties can be explained by catalysis by the\nnanoparticles rich in Ti, Zr or Al located on the surface of Mg grains. They provide effective pathways for the\nhydrogen diffusion into the MgH2. The morphological and microstructural characteristics were investigated by\nscanning electron microscope Tescan Lyra 3 and by X-ray diffraction. The hydrogen sorption was measured\nby Sieverts method using Setaram PCT-Pro device.\nStudied experimental composite absorbed 4.2 wt.% H 2 at 573 K and 3 wt.% H 2 at 523K within 10 min. The\nhydrogen storage capacity of the composite was about 4.6% wt.% H 2 and 4.2% wt.% H 2 at 573K and 523K,\nrespectively.
HYDROGENATION PROPERTIES OF BALL-MILLED Mg-Ti-C-Zr COMPOSITE
Král, Lubomír ; Čermák, Jiří ; Roupcová, Pavla
The hydrogen storage properties of ball-milled Mg-Ti-Zr-C composite (1.8 wt.% Ti, 1.9 wt.% Zr and 0.2 wt.% C) were investigated. It has been previously shown, that the addition of Ti, Zr and C improved its storage properties. This beneficial effect of additives upon hydrogen storage properties can be explained by catalysis by the particles rich in Ti or Zr located on the surface of Mg grains. They provide effective pathways for the hydrogen diffusion into the MgH2. The morphological and microstructural characteristics were investigated by scanning electron microscopy and by X-ray diffraction. The hydrogen sorption was measured by Sieverts method using Setaram PCT-Pro device. In this paper, sorption behaviour of the composite after ball-milling and after aging on the air was compared. The ball-milled composite adsorbed 3.5 wt.% H2 within 10 min at 623 K. However, hydrogen storage capacity of the composite aged on the air for 7 months remarkably decreased: The aged composite adsorbed within 10 min only 2 wt.% H2 at 623 K and the sorption capacity decreased from 4.7 wt.% H2 to 2.1 wt.% H2.
HYDROGEN ABSORPTION IN A-Co30Fe55B15
Čermák, Jiří ; Král, Lubomír ; Roupcová, Pavla
Hydrogen solved in amorphous alloys (AAs) influences their magnetic characteristics. AAs are also perspective\nas additives that can improve hydrogen storage kinetic in certain types of ball-milled hydrogen storage\nmaterials (HSMs). Therefore, knowledge of hydrogen solubility and hydrogen sorption kinetics in AAs are of a\ngreat importance for aimed design both AAs with optimal magnetic parameters and HSMs with desired sorption\ncharacteristics. In the present paper, amorphous alloy Co30Fe55B15 (an example of the type a-TM1xTM2y Bz ;\nTM - transition metal) was investigated. Hydrogen concentration c H was measured by Sieverts method in\ntemperature interval from T = 150 °C to T = 350 °C under hydrogen pressure p up to 6 MPa. It was found that\nc H was an increasing function of p and its maximum value was typically 0.5 wt.% H2 at 350 °C and 6 MPa.\nHowever, when the alloy was preliminary hydrogen charged (PHC), the pressure dependence of total c Htot in\nthe first absorption cycle(s) is non-monotonous in dependence on PHC conditions. For the sake of comparison,\nthe same absorption characteristics were measured also in Mg2Ni intermetallic that is a common constituent\nin Mg-based HSMs. Comparing Co30Fe55B15 and Mg2Ni, it was concluded that Co30Fe55B15 shows lower\nhydrogen solubility, but much better absorption kinetics.
IFRS a česká účetní legislativa
Fabiánová, Monika ; Král, Ing Lubomír (oponent) ; Fedorová, Anna (vedoucí práce)
Diplomová práce obsahuje transformaci účetních výkazů dle české účetní legislativy obchodní korporace XY, s. r. o. na účetní výkazy, jež jsou v souladu s Mezinárodními standardy účetního výkaznictví. Diplomová práce je rozdělena na 4 části. První částí jsou teoretická východiska, ve kterých jsou popsány rozdíly mezi Českou účetní legislativou a IFRS. Vybrané rozdíly jsou zvoleny na základě položek v účetních výkazech obchodní společnosti, vzniklé rozdíly jsou dále použity pro práci v druhé části diplomové práce. V praktické části je provedena analýza účetních výkazů obchodní společnosti. Na základě porovnání českých a mezinárodních standardů jsou zde uvedeny změny, které jsou nutné k převodu účetních výkazů. Závěrem diplomové práce je zhodnocení dané problematiky a dopadů na danou obchodní společnost.
HYDROGEN STORAGE IN Mg-In-C ALLOYS: EFFECT OF COMPOSITION AND AGEING
Čermák, Jiří ; Král, Lubomír
Hydrogen storage in two Mg-In-C alloys with different In concentration, c In , was studied in the temperature range from 250°C to 350°C after five-years-ageing at room temperature. The both alloys show acceptable cycling stability, however, the storage capacity of the alloys decreased from about 5 wt. % H2 to about 2,5 and 3.1 wt. % H 2 by higher c In and lower c In , respectively after 5 years. The sorption kinetics degraded much more by high c In than by c In . PCT isotherms, TPS and DSC patterns were measured for both materials. It was found that the hydrides responsible for hydrogen storage in alloy with higher c In are slightly more stable.
The Changes in Structure of Steel P91 after Short Annealings
Král, Lubomír ; Čermák, Jiří ; Král, Petr
Phase composition of the steel P91 during annealing was studied with the aim to reveal the evolution of new phases. In this paper, the precipitation was characterized using energy-dispersive X-ray spectroscopy (EDS) and electron diffraction in transmission microscopy (TEM). Only Nb-rich particles were found in the studied samples austenitized at 1423 °C for 20h and water cooled. After tempering at 673 °C for 2 h, the formation mainly M3C type carbides and after tempering at 873 °C for 2 h, the formation of M7C3 and M23C6 was observed. These structure changes play an important role for stability and also carbon diffusion.
CARBON DIFFUSION IN CARBON-SUPERSATURATED 9CR-1MO STEEL: ANOMALOUS TEMPERATURE DEPENDENCE OF CARBON DIFFUSIVITY
Čermák, Jiří ; Král, Lubomír
Carbon diffusion was studied in temperature interval 573 - 1073 K in carbon-supersaturated surface layer of 9Cr–1Mo steel P91 and in model Fe-15Cr binary alloy. Extremely low carbon diffusion coefficient D (by 3 orders of magnitude lower than the value D eq in material with equilibrium carbon concentration) was observed in carburized surface region of Fe-15Cr. Similar results were obtained for P91 above the temperature T n ~ 800 K. However, below T n , the values of D measured in P91 increased and approached the value of D eq . It seems that the non-Arrhenius behaviour of P91 steel around T n may be ascribed to the α → α + α’ phase decomposition. Possible effect of nitrogen upon the low-temperature increase in D in P91 steel was excluded.
Initial Stage of Mutual Diffusion of Carbide in Iron
Čermák, Jiří ; Král, Lubomír
Initial stage of mutual diffusion close to carbon/iron interface was investigated in the present work. SIMS technique of concentration profiles enabled to study the carbon redistribution in the very early stages, when the diffusion process occurs – at least partly – in regions, where the carbon concentration exceeds the carbon concentration limit. It was observed that carbon diffusion coefficients are much lower under such conditions, than in Fe matrix with equilibrium carbon concentration. The measured carbon diffusion coefficients approached values reported for carbon diffusion in carbides.
Comparison of Diffusion Coefficients in Initial Stages of Mutual Diffusion in Layered Structures Carbon/Ferrite and Carbon/Austenite for Chosen Alloys
Čermák, Jiří ; Král, Lubomír
Coefficients of mutual carbon diffusion were measured at initial stages of diffusion for surface thin layer of carbon/ferrite and carbon surface layer/austenite. The aim of the study was to compare the diffusion characteristics obtained at the present strongly non-equilibrium case with those known for carbon mutual diffusion in cases where the carbon concentration does not exceed the solubility limit in the respective substrate. The second goal was to judge, whether the carbon diffusivity is determined by the structure of the substrate matrix (BCC or FCC). As examples of ferrite substrate, pure Fe and chromium steel P91 were chosen, as an example of austenite substrate, AISI316 was taken. It was obtained that – similar to nearequilibrium case – the carbon diffusion measured close to interface C/austenite is significantly lower compared to carbon diffusion near the C/ferrite. Values of carbon diffusion coefficients in cases C/Fe and C/P91 are close one to another. All carbon diffusion coefficients are much lower than those, reported for near-equilibrium conditions; they approach values measured in carbides.
Measurement of Carbon Diffusion Coeficient - Calibration of Sputter Depth
Král, Lubomír ; Čermák, Jiří
Depth profiling mode of MiniSIMS device was applied to diffusion measurement. Calibration of crater depth was done using shearing interference microscope Zeiss Epival Interphako (ZEI) and confocal mikroskope Olympus LEXT OLS3100 with atomic force microscopy (AFM) modul. The ZEI uses one of the classical interferometric measuring methods. Generally this method leads to results with considerable experimental error. AFM is a very high-resolution type of scanning probe microscopy, with typical resolution of the order of fractions of nanometers, which is more than 1000 times better than the optical diffraction limit. However, the results taken by ZEI were in agreement with much more precise results of surface profiling achieved by AFM. It was found, at given experimental conditions (Fe-rich matrix, Ga + primary ions, 5 kV/3nA, DWT=1), that the sputter rate is some 0.3 nm per a single sputter scan of the crater area (50x50 µm). This depth calibration with SIMS technique can be applied to the study of carbon diffusion in BCC iron as an example. Special technique was developed, which avoids radio-tracer measurements with C-14. Obtained results are lower than the extrapolated values, which may be due to limited solubility of carbon in iron.

Národní úložiště šedé literatury : Nalezeno 32 záznamů.   předchozí11 - 20dalšíkonec  přejít na záznam:
Viz též: podobná jména autorů
3 KRÁL, Libor
3 Král, L.
1 Král, Ladislav
5 Král, Luboš
8 Král, Lukáš
3 Kráľ, Libor
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