Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "Przybylski, K." wg kryterium: Autor


Wyświetlanie 1-4 z 4
Tytuł:
Electrical properties of BaCeO₃-based electrolytes for use in dual protonic ceramic-solid oxide fuel cells
Autorzy:
Gawel, R.
Przybylski, K.
Powiązania:
https://bibliotekanauki.pl/articles/1055096.pdf
Data publikacji:
2017-05
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
composites
electrolytes
ceramics
electrochemistry
Opis:
Bulk samples consisting of BaCe_{0.85}Y_{0.15}O_{3-δ} (BCY15) and Ce_{0.85}Y_{0.15}O_{2-δ} (YDC15) compounds, mixed together in different ratios, were studied as potential electrolytes in dual protonic ceramic-solid oxide fuel cells and compared with non-composite BCY15 and YDC15. The microstructures of the sintered materials indicate that BCY15 exhibits the largest grains, whereas composites have greater visible porosity than the non-composite samples. From X-ray diffraction studies it follows that BCY15 and YDC15 consist mainly of one phase, whereas the composites are two-phase materials. Electrochemical impedance spectroscopy studies at different temperatures show that the composite materials are capable of conduction the order of 10¯³ S/cm at temperatures above 500°C in a hydrogen-containing atmosphere. Furthermore, activation energy values of the conductivity determined for the composites in air atmosphere are between those obtained for BCY15 (E_{a}=0.590±0.017 eV) and YDC15 (E_{a}=1.132±0.008 eV). From this it follows that both phases of the composites influence the electrical conductivity of the materials. In conclusion, BCY15 and the BCY15-YDC15 composites show promise for future use as electrolytes in dual protonic ceramic-solid oxide fuel cells.
Źródło:
Acta Physica Polonica A; 2017, 131, 5; 1361-1366
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Structure of Aqueous Solutions of 1,2-, 1,3- and 1,4-Butanediol Investigated by Positron Annihilation and Ultrasonic Methods
Autorzy:
Jerie, K.
Baranowski, A.
Gliński, J.
Orzechowski, K.
Przybylski, J.
Powiązania:
https://bibliotekanauki.pl/articles/2024276.pdf
Data publikacji:
2001
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
61.25.Em
78.70.Bj
Opis:
The structure of aqueous solutions of 1,2-, 1,3- and 1,4-butanediol was investigated using adiabatic compressibility measurements and positron annihilation methods. In the case of 1,2-butanediol the experimental results are very similar to those obtained earlier for systems where hydrophobic hydration dominates. In other cases there are evidences for increased rigidity of the water network, which arises from formation of hydrogen bonds between diols and water. Usefulness of both the methods applied in investigating the structure of liquid solutions was proved.
Źródło:
Acta Physica Polonica A; 2001, 99, 3-4; 393-398
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Hydrophobic-Like Solvation in Non-Aqueous Solutions: Positron Annihilation in and Compressibility of Tert-butanol and Tetramethylurea in Ethylene Glycol
Autorzy:
Jerie, K.
Baranowski, A.
Gliński, J.
Przybylski, J.
Powiązania:
https://bibliotekanauki.pl/articles/2024269.pdf
Data publikacji:
2001
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
61.25.Em
78.70.Bj
Opis:
The pioneer experimental results of positron annihilation experiments in non-aqueous solutions of tetramethylurea and tert-butanol were compared to those of ultrasonic velocity. For tert-butanol, the positron annihilation results exclude existence of hydrophobic-like interactions and formation of weak, labile crystalline-like solvates in solution. For tetramethylurea solute the changes of annihilation parameters with concentration are minor and only limited conclusions can be drawn on this system, while they are stronger for tert-butanol solute. However, all the above is consistent with an assumption that the more hydrophobic solute (tert-butanol) should affect the original glycol structure stronger than that interacting with glycol via hydrogen bondings only. On the other hand, the ultrasonic data for the systems tested, although very precise, hardly confirm formation of any specific structure. It is possible, however, that the solvates do not differ in their compressibility from the pure liquids, and/or are formed only in very small amounts. Thus, usefulness of the positron annihilation method in investigation of liquid structure was proven.
Źródło:
Acta Physica Polonica A; 2001, 99, 3-4; 385-392
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Comparative Study of Orientational Order of Some Liquid Crystals from Various Homologous Series
Autorzy:
Bielejewska, N.
Chrzumnicka, E.
Mykowska, E.
Przybylski, R.
Szybowicz, M.
Władysiak, K.
Bauman, D.
Powiązania:
https://bibliotekanauki.pl/articles/2047169.pdf
Data publikacji:
2006-12
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
61.30.Gd
33.20.Fb
33.20.Kf
33.50.Dq
Opis:
The long-range orientational order of liquid crystals from homologous series of 4-n-alkyl-4'-cyanobiphenyl, 4-n-alkoxy-4'-cyanobiphenyl, trans-4-n-alkyl(4'-cyano-phenyl)-hexane, and 4-(trans-4'-n -alkylcyclohexyl)-isothiocyanato-benzene was studied by means of classical methods of optical spectroscopy: absorption of the polarized light, fluorescence depolarization, and Raman scattering depolarization. The absorption, emission, and Raman scattering spectra of linearly polarized light were recorded as a function of temperature in the whole range of the mesophase. On the basis of these spectra the order parameters ⟨P$\text{}_{2}$⟩ and ⟨P$\text{}_{4}$⟩ as well as the orientational distribution function were determined. The results obtained for members of various series with the same number of carbon atom in the alkyl chain were compared. It was found that the orientational order of liquid crystal molecules depends on the structure of the rigid core, on the kind of the terminal group as well as on the alkyl chain length. The odd-even effect for the order parameters, explained as the alteration of interaction between alkyl chains, was observed.
Źródło:
Acta Physica Polonica A; 2006, 110, 6; 777-793
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies