The Influence of Corrosion in an Aqueous Solution of NaCl on Fracture and Strength of Various Structural Ceramics

Abstract

The present work studies the corrosion of three most widely used types of structural ceramics – silicon nitride, solid state sintered alumina and liquid phase sintered alumina – in 3 % aqueous solutions of sodium chloride at temperatures up to 290 °C and pressures up to 7 MPa. The corrosion of silicon nitride was controlled by attack of Si3N4 matrix grains, while yttrium oxynitride amorphous grain boundary phase was corrosion resistant. Corrosion of Si3N4 in reference media -distilled water - at 290 °C was characteristic by formation of passivation layer, which hindered further dissolution of silicon nitride matrix. The presence of sodium chloride resulted in formation of discontinuous layer of corrosion products, resulting in more severe corrosion than in distilled water. The corrosion of liquid phase sintered alumina was mainly attributed to congruent dissolution of SiO2 and CaO from grain-boundary amorphous film, which was accelerated at higher temperature, and accompanied by precipitation of siliceous phases from oversaturated solution at 200 °C. Pure polycrystalline alumina corroded by loss of alumina grains, which did not dissolve in the corrosion media. The corrosion impaired significantly the fracture strength of silicon nitride, creating new, corrosion related defects at the surface, while the influence of corrosion on fracture strength of polycrystalline aluminas was negligible.

Corrosion and Low Temperature Degradation of 3Y-TZP dental ceramics under acidic conditions

“…Additional corrosion tests in water at 80 °C for 40 days were carried out for IVOCLAR and leaching solutions were also analyzed by ICP-MS. The concentration of leached ions (Qit) was calculated according to the formula: The normalization (NLit) of the concentration of the leached ion (Qit) to its content in the material itself (wi) provides information on the dissolution of the material as a whole, or whether or not the preferential dissolution of any of the present phases, either crystalline or glassy, can be assessed [22].…”