Properties of hydrogen permeation barrier on the surface of zirconium hydride

A hydrogen permeation barrier was manufactured by the in situ reaction of zirconium hydride with oxygen. A reduction in the hydrogen permeation of the oxide films was detected by measuring the mass difference of the zirconium hydride samples after the dehydrogenation experiment. The reaction of zirconium hydride with oxygen occurs only under the condition that the temperature is higher than 673 K in the oxygen partial pressure of 0.1 MPa. The oxide film is composed of two layers, a permeable oxide layer and a dense oxide layer, and the main phase of the oxide film is ZrO2 with baddeleyite structure. The XPS analysis shows that O-H bonds exist in the oxide film, which are helpful for resisting hydrogen diffusion through the oxide film.

Improvement of hydrogen permeation barrier performance by iron sulphide surface films

Fe–S compounds with hexagonal crystal structure are potential hydrogen permeation barrier during H2S corrosion. Hexagonal system Fe–S films were prepared on carbon steel through corrosion and CVD deposition, and the barrier effect of different Fe–S films on hydrogen permeation was tested using electrochemical hydrogen permeation method. After that, the electrical properties of Fe–S compound during phase transformation were measured using thermoelectric measurement system. Results show that the mackinawite has no obvious barrier effect on hydrogen penetration, as a p-type semiconductor, and pyrrhotite (including troilite) has obvious barrier effect on hydrogen penetration,as an n-type semiconductor. Hydrogen permeation tests showed peak permeation performance when the surface was deposited with a continuous film of pyrrhotite (Fe_(1–x)S) and troilite. The FeS compounds suppressed hydrogen permeation by the promotion of the hydrogen evolution reaction, semiconducting inversion from p-to n-type, and the migration of ions at the interface.

Characterization of ZrO_(2) ceramic coatings on ZrH1.8 prepared in different electrolytes by micro-arc oxidation

ZrO_(2)ceramic coatings were directly prepared on the surface of ZrH_(1.8) in silicate and phosphate elec-trolytes by micro-arc oxidation(MAO)technique,respec-tively.The microstructure,chemical composition and phase composition of ZrO_(2)ceramic coatings were inves-tigated by X-ray diffraction(XRD),energy-dispersive spectrometry(EDS)and scanning electron microscopy(SEM).The anti-permeation effect was measured by means of vacuum dehydrogenation experiment.It is found that the coating fabricated in phosphate electrolyte is more compact than that in silicate electrolyte.The coatings fabricated on the surface of ZrH_(1.8) are composed of M-ZrO_(2),T-ZrO_(2) and C-ZrO_(2).EDS analysis indicates that the coatings are mainly composed of O and Zr.Vacuum dehydrogenation experiment shows that the permeation reduction factor(PRF)of coating prepared in phosphate electrolyte is su-perior to that in the silicate electrolyte,and the PRF value reaches up to 11.2,which can enhance the resistance effect of hydrogen significantly.