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Objectives This study was intended to separate residual stresses arising from the mismatch in coefficients of thermal expansion between glass and zirconia (ZrO2) from those stresses arising solely from the cooling process. Slow crack growth experimentes were undertaken to demonstrate how cracks grow in different residual stress fields. Methods Aluminosilicate glass discs were sintered onto ZrO2 to form glass–ZrO2 bilayers. Glass discs were allowed to bond to the ZrO2 substrate during sintering or prevented from bonding by means of coating the ZrO2 with a thin boron nitrade coating. Residual stress gradients on “bonded” and “unbonded” bilayers were assessed using birefringence measurements. Unbonded glass discs were further tested under biaxial flexure in dynamic fatigue conditions in order to evaluate the effect of residual stress on the slow crack growth behavior. Results When fast-ccoling was induced, residual tensile stresses on the glass increased significantly on the side toward the ZrO2 substrate. By allowing the bond between glass and ZrO2, those tensile stresses observed in unbonded specimens are overwhelmed by the contraction mismatch stresses between the ZrO2 substrate and the glassy overlayer. Specimens containing residual tensile stresses on the bending surface showed a time-dependent strength increase in relation to stress-free annealed samples in the dynamic biaxial bending test, with this effect being dependent on the magnitude of the residual tensile stress. The phenomenon observed is explained here on the basis of the water toughening effect, in which water diffuses into the glass promoting local swelling. An additional residual tensile stress at the crack tip adds an applied-stress-independent (Kres) term to the total tip stress intensity factor (Ktip), increasing the stress-enhanced diffusion and the shielding of the crack tip through swelling of the crack faces. Significance Residual stresses in the glass influence the crack growth behavior of veneered-ZrO2 bilayered dental prostheses. The role of water in crack growth might be of higher complexity when residual stresses are present in the glass layer.

Objectives The aim was to evaluate the polymerization properties of bulk-fill resin composites using two different light-curing protocols, in terms of degree of conversion (%DC), Vickers hardness (HV), polymerization volume shrinkage (PVS) and polymerization shrinkage stress (PSS) and compare them to conventional condensable and flowable resin composites. Materials and methods Filtek BulkFill (FBF, 3MESPE, Germany), SDR (Dentsply, Germany), TetricEvoCeram BulkFill (TBF, Ivoclar-Vivadent, Liechtenstein), Venus BulkFill (VBF, Heraeus, Germany), X-traBase (XTB, Voco, Germany), FiltekZ250 (3MESPE) and Filtek Supreme XTE Flowable (FSF, 3MESPE) were investigated. Light-curing was performed for 30 s or according to manufacturers’ instructions (1200 mW/cm2, Bluephase20i, Ivoclar-Vivadent). For %DC and HV, discs (n = 5) of 2 or 4 mm in thickness were prepared and stored for 24 h in distilled water at 37 °C. %DC was determined by FTIR-ATR-spectroscopy. %DC and HV were measured at the top and bottom of the specimens. PVS was measured using Archimedes method (n = 6). PSS measurements (n = 10) were carried out using 5 mm diameter PMMA rods as bonding substrates with a specimen height of 1 mm in a universal testing machine. Data were analyzed using one- and two-way ANOVA (α = 0.05). Results Except Z250 in the manufacturers’ light-curing mode, all materials showed no significant inferior %DC at 4 mm thickness. When light cured for 30 s Z250 had no significant differences in %DC at 2 or 4 mm when compared to top. FBF, TBF, FSF and Z250 displayed significant reduced HV at 4 mm in both curing modes. Z250 and TBF showed the lowest PVS and FSF the highest PSS in both curing modes. Significance All investigated bulk-fill composites obtained sufficient polymerization properties at 4 mm depth. Enhanced curing time improved the investigated polymerization properties of bulk-fills and Z250.

Objective The aim of this study was to evaluate if pH-neutralization behavior of self-adhesive resin cements has an influence on their mechanical properties. Methods pH-neutralization, water sorption, solubility and flexural strength of G-Cem Automix (GCA), G CEM Capsules (GCC), Maxcem Elite (MCE), RelyX Unicem Clicker (RXC), RelyX Unicem Maxicap (RXM), RelyX Unicem 2 (RX2), and Speed-Cem (SPC) were tested in self-curing mode. Specimen's pH-values were recorded up to 24 h with a pH-electrode. Water sorption (WS) and solubility (SO) were measured. Flexural strength (FS) was evaluated before and after thermocycling (TC) and fracture surfaces analyzed under SEM. Results RX2 (pH 24 5.89), RXC (pH 24 5.49) and SPC (pH 24 5.42) showed highest 24 h pH-values, followed by GCA (pH 24 5.34). Capsulated products and MCE (pH 24 3.90) reached lower pH-values. GCC (75.78 μg/mm 3 ) showed the highest WS followed by MX (69.64 μg/mm 3 ), RXM (64.76 μg/mm 3 ), GCA (25.86 μg/mm 3 ) and SPC (30.42 μg/mm 3 ). Capsulated products RXM (56.58 μg/mm 3 ) and GCC (30.94 μg/mm 3 ) presented the highest SO, GCA (4.06 μg/mm 3 ) and SPC (4.26 μg/mm 3 ) revealed the lowest. GCA (114.03 MPa) had the highest initial FS followed by SPC (79.81 MPa), RXM (41.61 MPa) the lowest. FS of all materials decreased significantly after TC except for RXC (44.65 MPa) and RX2 (65.92 MPa). FS of GCC (16.47 MPa) and MCE (28.21 MPa) decayed the most. A highly linear correlation was observed between percentage decrease of FS after TC and 24 h pH-values ( R 2 = 0.861). Significance Within the limits of this study pH-neutralization behavior has an influence on mechanical stability. When using self-adhesive resin luting agents, automix-syringe products with improved pH-neutralization behavior should be favored.