Abstract

Tricalcium silicate-based cements (TCS-BC) have reached great relevance in modern dentistry, where they are used in root-end filling or perforation repair treatments, and also for restoring deep and/or voluminous coronary carious lesions, among other applications. In some TCS-BC such as BiodentineTM, the physical and chemical properties, e.g. high compressive strength, have led to consider this cement as a dentine substitute. One of the drawbacks of BiodentineTM is its very high washout; which refers to the tendency of disintegrate at initial stage of hydration upon early contact with blood or other fluids, just at the moment after it is still as a freshly prepared paste. The present research was focused to compare properties related to workability and hardening at early stages of hydration of experimentally synthetized nano-sized tricalcium silicate (nTCS) and BiodentineTM (BIOD). Both pastes were tested for hardening at 0, 1, 2 and 3 h of hydration, using a penetration test adapted from standards D3441-79 and D1558-84. The hydrated products were evaluated by X-ray diffraction (XRD), thermogravimetry (TG) and 29Si NMR spectroscopy; pH measurements were taken along 28 days of hydration. The set cement pastes were evaluated for sealing ability and microleakage. Following literature reports, the CSH phase as a hydration product, was identified and modeled in both cements as defective clinotobermorite Ca11Si9O28(OH)2·8.5H2O. The CSH phases obtained differ from each other by its microstructural arrangement and packing densities, which depend on the w/c ratio of nTCS and BIOD pastes, which were 0.5 and 0.36 respectively. The hardening of BIOD is significantly influenced by its w/c ratio with a hydration fluid that presumably contains about 0.05% of polycarboxylate-based superplasticizer, which was identified by Raman spectroscopy. The washout and hardening properties were pictured by and scheme for flocculation, w/c ratio, and packing density of the CSH particles characterizing the cement pastes.

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