Informacja

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

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


Wyświetlanie 1-2 z 2
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
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
    Wyświetlanie 1-2 z 2

    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