Partially stabilised zirconia (PSZ) has received special attention due to i
ts high strength, high corrosion and erosion resistance, and high resistanc
e to fracture. The phase transformations of ZrO2 in its application process
have long been known to be important. Various physical, hydrothermal, and
chemical effects can cause the phase transformations. Although many advance
s have been made in recent years in the understanding of the effects, found
ations and mechanisms of the ZrO2 phase transformation, however, no study h
as yet reported on the phase transformation from t-ZrO2 to m-ZrO2 in corros
ion solution at room temperature. In the present study, both the corrosion
resistance of ZrO2 and the ZrO2 phase transformation in a corrosive solutio
n (1.5% HF + 5% HCl) used in the oil industry to clean downhole pipes were
investigated. The erosion behaviours of PSZ-ZrO2 before and after corrosion
have been studied using a SiC/water slurry jet impingement test rig with t
he aim of providing some information on the material's response to erosion
attack. SEM and X-ray were used to characterise the microstructure of the c
orroded layer, and phase change after corrosion. After corrosion, the peaks
of monoclinic structures increase dramatically; ZrCl4 or ZrF4 were not det
ected. By increasing the length of corrosion time, the monoclinic structure
is markedly increased. Thus, the corroded layer is the main source contrib
uting to the increase in the monoclinic phase. The possible reaction steps
in HF + HCl solution are discussed. The mechanism of t-m phase transformati
on is discussed in this work. From the thermodynamic viewpoint, a phase str
ucture would tend to transform from the metastable phase to the more stable
under the attack of a corrodent, or under impact stress or tensile stress.
However, the difference between the two cases is that during the transform
ation induced by impacting stress, part of the t-ZrO2 transforms into m-ZrO
2 and microcracks develop, which consume crack propagation energy and relea
se stress concentration, while t-m transformation due to the corrosion proc
ess forms a porous m-zirconia layer. Microstructural evaluation as well as
chemical analysis shows that the surface structure of PSZ-ZrO2 changes and
becomes more porous during corrosion process, not only due to the t-m phase
transformation, in which cracks and voids are anticipated owing to 3%-5% v
olume change; but also due to the effect of higher corrosion rates of addit
ives in PSZ-ZrO2 as well. The erosion behaviours of PSZ-ZrO2 before and aft
er corrosion, using a SiC/water slurry jet, are also compared with other ce
ramic materials. (C) 1999 Elsevier Science S.A. All rights reserved.