2026-05-27T04:43:06Zhttps://riuma.uma.es/rest/oai/request

oai:riuma.uma.es:10630/97842026-02-03T10:52:44Zcom_10630_2254col_10630_37953

Mechanism of stabilization of dicalcium silicate solid solution with aluminium Cuesta-García, Ana María García-Aranda, Miguel Ángel Sanz, Jesús Gómez-de-la-Torre, María de los Ángeles Losilla, Enrique R. Químina inorgánica Stoichiometric dicalcium silicate, Ca2SiO4, displays a well-known polymorphism with temperature. When this phase is doped by a range of elements, belite, one of the main phases of cements, is generated. Here, we thoroughly study the aluminum doping of dicalcium silicate. This type of study is important for cement characterization and also from a basic point of view. Ca2Si1−2xAl2xO4−x□x (x = 0, 0.010, 0.014, 0.03) has been prepared and studied by X-ray powder diffraction and the Rietveld method. The limiting composition has been established as Ca2Si0.972Al0.028O3.986□0.014. The 27Al MAS NMR band located close to ∼−70 ppm is ascribed to tetrahedral environments, in agreement with the proposed aliovalent Si/Al atomic substitution mechanism. Thermal analysis measurements under a wet atmosphere indirectly confirm the increase of oxygen vacancies as the amount of incorporated protons increases with the aluminium content. A thorough electrical characterization has been carried out including overall conductivity measurements under wet and dry atmospheres and conductivity as a function of the oxygen partial pressure. The samples show oxide anion conductivity with a small p-type electronic contribution under oxidizing conditions. These compounds display a very important proton contribution to the overall conductivities under humidified atmospheres. 2015-05-15T08:48:37Z 2015-05-15T08:48:37Z 2015 2013-11-11 journal article 1477-9226 http://hdl.handle.net/10630/9784 eng open access ELSEVIER