Abstract

The magnesia (MgO) hydroxylation behavior in dilute suspensions (below 50% volumetric solid loads) has been extensively studied over the past decades due to its role in refractory castables. However, its equivalent effects on concentrated systems have not been analyzed in such a systemic way, although they are known to be as or more deleterious than those observed in dilute systems. This study focuses on the hydroxylation behavior of different sources of magnesia (sinter and caustic magnesia) in aqueous suspensions prepared at various solids concentrations (17-96 vol%) and shaped by distinct methods. They were analyzed by thermogravimetry, apparent volumetric expansion measurements, X-ray diffraction, scanning electron microscopy, and in situ temperature measurements during curing. The ratio between experimental and theoretical extents of the hydroxylation degree resulted in the reaction yield. A comparison between samples containing the same water amount revealed those with caustic magnesia showed a faster evolution of hydroxylation degree, apparent volumetric expansion, and higher maximum internal temperature during curing. In both systems, the yield levels of compositions of heavier solid loads were higher, despite the small quantity of hydroxylation products formed. Significant differences in the products’ microstructure were observed and related to the ions' mobility toward crystallization nuclei.

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