DSpace À propos de l'application DSpace
 

Depot Institutionnel de l'UMBB >
Publications Scientifiques >
Publications Internationales >

Veuillez utiliser cette adresse pour citer ce document : http://dlibrary.univ-boumerdes.dz:8080/handle/123456789/6021

Titre: Cu2O addition and sintering temperature dependence of structural, microstructural and dielectric properties of CaCu3Ti4O12 ceramics
Auteur(s): Djafar, Rabah
Boumchedda, K.
Chaouchi, A.
Fasquelle, D.
Sedda, K.
Brahimi, S.
Khalfaoui, K.
Bououdina, M.
Mots-clés: Ceramics
CCTO
Powder metallurgy
XRD and SEM
Dielectric properties
Date de publication: 2020
Editeur: Elsevier
Collection/Numéro: Materials Chemistry and Volume 256, 1 December 2020, 123706;
Résumé: This study is aimed in the replacement of commonly used (CuO) by Cu2O in the synthesis of perovskite CaCu3Ti4O12 (CCTO) phase by the solid-state reaction method. The XRD analysis of powder calcined at 1100 °C and ceramics sintered at different temperatures show that the CCTO phase was well crystallized with the presence of small quantities of additional phases. The SEM/EDS analysis of prepared pellets show that the formation of Cu2O/CuO phase occurs above 950 °C, resulting in enhanced densification at 1050 °C (>96%). However, it is found that the Cu2O-based CCTO begins to degrade around 1090 °C. The densification after sintering at 1050 °C reaches 96%, meanwhile dielectric constant and loss tangent values are optimum in the low frequency range (<103 Hz); i.e. 13378 and 0.177, respectively. This favors the use of Cu2O instead of CuO in CCTO ceramics for applications at low frequencies
URI/URL: http://dlibrary.univ-boumerdes.dz:8080/handle/123456789/6021
ISSN: 02540584
Collection(s) :Publications Internationales

Fichier(s) constituant ce document :

Fichier Description TailleFormat
Cu2O addition and sintering temperature dependence.pdf106,26 kBAdobe PDFVoir/Ouvrir
View Statistics

Tous les documents dans DSpace sont protégés par copyright, avec tous droits réservés.

 

Valid XHTML 1.0! Ce site utilise l'application DSpace, Version 1.4.1 - Commentaires