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Zastosuj identyfikator do podlinkowania lub zacytowania tej pozycji: http://hdl.handle.net/20.500.12128/12041
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dc.contributor.authorSzafraniak-Wiza, Izabela-
dc.contributor.authorDzik, Jolanta-
dc.contributor.authorBochenek, Dariusz-
dc.contributor.authorSzalbot, Diana-
dc.contributor.authorAdamczyk-Habrajska, Małgorzata-
dc.date.accessioned2020-01-17T16:09:32Z-
dc.date.available2020-01-17T16:09:32Z-
dc.date.issued2020-
dc.identifier.citation"Materials" 2020, iss. 2, art. no. 401, s. 1-13pl_PL
dc.identifier.issn1996-1944-
dc.identifier.urihttp://hdl.handle.net/20.500.12128/12041-
dc.description.abstractAlkaline based materials have been considered as a replacement for environmentally harmful Pb(Zr,Ti)O3 (PZT) electro‐ceramics. In this paper, the K1/2Na1/2NbO3 (KNN) ceramics were prepared in a three stage process: first Nb2O5, Na2CO3, and K2CO3 were milled in a high energy mill (shaker type) for different periods, between 25 h and 100 h, consecutively a solid state reaction was carried out at 550 °C. Finally, the uniaxially pressed samples were sintered at 1000 °C. The reaction temperature is lower for mechanically activated powders than in the case of the conventional solid‐state method. The ceramic samples, prepared from the mechanically activated powders, were investigated by dielectric spectroscopy. The influence of the duration of the mechanical activation on the properties of the ceramic materials, e.g., ceramic microstructures, phase transition temperatures, character of the temperature dependences of dielectric permittivity, are discussed.pl_PL
dc.language.isoenpl_PL
dc.rightsUznanie autorstwa 3.0 Polska*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/pl/*
dc.subjectLead‐free materialspl_PL
dc.subjectPerovskitespl_PL
dc.subjectMechanical activationpl_PL
dc.subjectPotassium sodium niobatepl_PL
dc.titlePreparation and dielectric properties of K1/2Na1/2NbO3 ceramics obtained from mechanically activated powderspl_PL
dc.typeinfo:eu-repo/semantics/articlepl_PL
dc.identifier.doi10.3390/ma13020401-
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Uznanie Autorstwa 3.0 Polska Creative Commons Creative Commons