КІНЕТИКА ДЕГАЗАЦІЇ I ПОГЛИНАННЯ ВОДНЮ ПАЛАДІЄМ У МОЛЕКУЛЯРНОМУ ТА ЕЛЕКТРОЛІЗНОМУ РЕЖИМАХ
DOI:
https://doi.org/10.15407/dopovidi2026.02.046Ключові слова:
водень, паладій, електроліз, енергія активації, абсорбція, газовиділенняАнотація
Experimental investigations of the kinetics of hydrogen saturation and outgassing from palladium have been carried out in conditions of interaction with molecular and electrolytic hydrogen at near room temperature and the pressure range of 1—2 at. Using the gravimetric method, it was established that the rate of hydrogen saturation during electrolysis is more than two orders higher than in the molecular driven regime. With help of massspectrometric method it has been shown that in the course of hydrogen absorption by Pd cathode during electrolysis and subsequent heating process in high vacuum, the ultrapure hydrogen (higher than 99.999 vol. %) is generated. Based on the measured temperature dependence of hydrogen evolution, the activation energy of hydrogen outgassing from the Pdcathode after onehour exposure to electrolysis ion current ≈8 A was calculated to be E ≈ 23 kJ/mol or ≈12 kJ/mol, in dependence on the temperature range (20—100 °C or 300—650 °C). The average value of activation energy for the whole temperature range of the performed measurements was estimated as ≈22.4 kJ/mol. Therefore, hydrogen outgassing from PdHx system could be multistage process with everchanging activation energy on time. The physicalchemical mechanisms and the influence of β ↔ α transition in the PdHx system are further discussed and analyzed to explain such hydrogen behavior during the outgassing process.
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