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The role of nano-perovskite in the negligible thorium release in seawater from Greek bauxite residue (red mud)

  • Platon N. Gamaletsos*
  • , Athanasios Godelitsas
  • , Takeshi Kasama
  • , Alexei Kuzmin
  • , Markus Lagos
  • , Theo J. Mertzimekis
  • , Jörg Göttlicher
  • , Ralph Steininger
  • , Stelios Xanthos
  • , Yiannis Pontikes
  • , George N. Angelopoulos
  • , Charalampos Zarkadas
  • , Aleksandr Komelkov
  • , Evangelos Tzamos
  • , Anestis Filippidis
  • *Šī darba korespondējošais autors

Pētījuma izpildes rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

27 Atsauces (Scopus)

Kopsavilkums

We present new data about the chemical and structural characteristics of bauxite residue (BR) from Greek Al industry, using a combination of microscopic, analytical, and spectroscopic techniques. SEM-EDS indicated a homogeneous dominant "Al-Fe-Ca-Ti-Si-Na-Cr matrix", appearing at the microscale. The bulk chemical analyses showed considerable levels of Th (111 μg g-1), along with minor U (15 μg g-1), which are responsible for radioactivity (355 and 133 Bq kg-1 for 232Th and 238U, respectively) with a total dose rate of 295 nGy h-1. Leaching experiments, in conjunction with SF-ICP-MS, using Mediterranean seawater from Greece, indicated significant release of V, depending on S/L ratio, and negligible release of Th at least after 12 months leaching. STEM-EDS/EELS & HR-STEM-HAADF study of the leached BR at the nanoscale revealed that the significant immobility of Th4+ is due to its incorporation into an insoluble perovskite-type phase with major composition of Ca0.8Na0.2TiO3 and crystallites observed in nanoscale. The Th LIII-edge EXAFS spectra demonstrated that Th4+ ions, which are hosted in this novel nano-perovskite of BR, occupy Ca2+ sites, rather than Ti4+ sites. That is most likely the reason of no Th release in Mediterranean seawater.

OriģinālvalodaAngļu
Raksta numurs21737
ŽurnālsScientific Reports
Sējums6
DOIs
Publikācijas statussPublicēts - 22 febr. 2016

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