Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Mechanisms of LiOH degradation and H{sub 3}BO{sub 3} repair of ZrO{sub 2} films

Conference ·
OSTI ID:479433
; ; ;  [1]
  1. Univ. of Toronto, Ontario (Canada). Centre for Nuclear Engineering

During a program to elucidate the mechanisms by which LiOH accelerates the corrosion of zirconium alloys and boric acid inhibits this effect, specimens were exposed to 0.01, 0.1, and 1.0 M LiOH solutions at 300 C (573 K) or 360 C (673 K) with and without the addition of boric acid. Results showed that local dissolution of the ZrO{sub 2} films formed pores whose depth was a function of the LiOH concentration and probably also of the temperature, alloy composition, and structure. Below a critical LiOH concentration, only superficial porosity was developed in short experiments. Above this critical concentration porosity develops throughout the initially impervious oxide and no pretransition corrosion kinetics are observed. Below this critical concentration, no effect of LiOH is observed on the pretransition oxidation kinetics until pores and cracks start to develop in the oxide prior to the oxidation rate transition. At this point LiOH can concentrate in the freshly developed pores by chemical extraction of water from the solution in the pores to form new ZrO{sub 2}. Once the critical LiOH concentration is reached in the pores, enlargement or extension of the pores can occur by dissolution. This process should occur beneath the relatively untouched pretransition oxide when the bulk solution is not concentrated enough to attack the oxide surface. Hydrothermal redeposition of much of the dissolved ZrO{sub 2} occurs on specimen surfaces or within the porous oxide. Boric acid has no effect on ZrO{sub 2} dissolution by LiOH. It is considered that in concentrated solutions the solubility product of some complex lithium zirconate borate can be exceeded and this can plug the pores. In dilute solutions, therefore, boric acid can only operate inside the porous oxide film, where the chemical concentration mechanism should be equally effective for both LiOH and H{sub 3}BO{sub 3}.

Sponsoring Organization:
Organization of CANDU Industries, Toronto, ON (Canada); Natural Sciences and Engineering Research Council of Canada, Ottawa, ON (Canada)
OSTI ID:
479433
Report Number(s):
CONF-950926--
Country of Publication:
United States
Language:
English

Similar Records

Oxidation and salt corrosion of an Si{sub 2}N{sub 2}O-ZrO{sub 2} composite material
Conference · Mon Dec 30 23:00:00 EST 1996 · OSTI ID:567567

Aqueous chemistry of lithium hydroxide and boric acid and corrosion of Zircaloy-4 and Zr-2.5Nb alloys
Book · Fri Dec 30 23:00:00 EST 1994 · OSTI ID:55662

Corrosion and anodic behavior of lithium in solutions of the system LiC1-LiOH-H/sub 2/O
Journal Article · Sun Mar 09 23:00:00 EST 1986 · J. Appl. Chem. USSR (Engl. Transl.); (United States) · OSTI ID:7037291