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This work was undertaken to evaluate the effects of dental grinding and sandblasting on the biaxial flexural strength and Weibull modulus of various Y-TZP ceramics containing 3 mol% yttria. In addition, the susceptibility of pristine and mechanically treated materials to low-temperature degradation under the conditions adopted for testing the chemical solubility of dental ceramics was investigated. The results revealed that surface grinding and sandblasting exhibit a counteracting effect on the strength of Y-TZP ceramics. Dental grinding lowered the mean strength and Weibull modulus, whereas sandblasting provided a powerful method for strengthening, but at the expense of somewhat lower reliability. The finest-grained material exhibited the highest strength after sintering, but it was less damage tolerant than tougher, coarse-grained materials. Upon extraction with the acetic acid solution and the ammonia solution, a significant amount of tetragonal zirconia had transformed to monoclinic, but extensive microcracking and attendant strength degradation had not yet occurred. Standard grade Y-TZP ceramics are more resistant in an alkaline than in an acidic environment, and there was a strong grain-size dependence of the diffusion-controlled transformation. Since a special Y-TZP grade containing a small amount of alumina exhibited the highest damage tolerance and superior stability in an acidic environment, this material shows considerable promise for dental applications.

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The purpose of this study was to evaluate the influence of contamination and subsequent cleaning on the bond strength and durability of an adhesive resin to nano-structured alumina-coated zirconia ceramic. Zirconia ceramic disks were coated with nano-structured alumina, utilizing the hydrolysis of aluminum nitride powder. After immersion in saliva or the use of a silicone disclosing agent, specimens were cleaned with phosphoric acid etching or with tap water rinsing only. Uncontaminated specimens served as controls. Plexiglas tubes filled with composite resin were bonded with a phosphate monomer [10-methacryloxydecyl-dihydrogenphosphate (MDP)]-containing resin (Panavia 21). Subgroups of eight specimens each were stored in distilled water at 37 degrees C, either for 3 d without thermal cycling (TC) or for 150 d with 37,500 thermal cycles from 5 to 55 degrees C. The tensile bond strength (TBS) was determined using a universal testing machine at a crosshead speed of 2 mm min(-1). The topography of the debonded surface was scrutinized for fractographic features, utilizing both optical and scanning electron microscopy. The TBS to uncontaminated nano-structured alumina-coated zirconia ceramic was durable, while contamination significantly reduced the TBS. Phosphoric acid cleaning was effective in removal of saliva contamination from the coated bonding surface but was not effective in removal of the silicone disclosing agent. Nano-structured alumina coating improves resin bonding to zirconia ceramic and eliminates the need for air-abrasion before bonding.

The reactivity of AlN powder in diluted inorganic acids was studied by measuring the pH and temperature during its hydrolysis. At very low starting pH (pH ϳ1) no reaction was observed, regardless of the acid used. In contrast, in a less acidic environment, i.e., at higher pH values (pH ϳ3), the reaction was fast enough to reveal the influence of different acids on the hydrolysis reaction. Monoprotonic acids which are completely dissociated (HCl, HF, HNO 3 ), and form watersoluble salts with aluminum, did not influence the hydrolysis reactions. In the presence of incompletely dissociated diprotonic H 2 SO 4 and H 2 CO 3 acids which form water-soluble salts with aluminum, the reaction was hindered but not prevented. In the presence of phosphoric acid the hydrolysis was prevented at room temperature, presumably because of the formation of insoluble phosphates on the powder surface. At elevated temperatures their solubility was substantial, and the reactivity of AlN powder in a diluted hot phosphoric acid was reestablished. In the presence of silicic acid the reaction was suppressed at both room and elevated temperatures, which was also ascribed to the formation of insoluble silicates. The adsorption of silicate anions onto the powder surface was confirmed by chemical analysis and zeta potential measurement. Using DRIFT measurements, however, the presence of Si-O bonds on the powder could not be unambiguously confirmed, since the characteristic wavelengths for these bonds are in the region of very strong Al-N stretching frequencies.

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