Nickel stabilization efficiency of aluminate and ferrite spinels and their leaching behavior

Kaimin Shih, Tim White, James O. Leckie*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

98 Citations (Scopus)

Abstract

Stabilization efficiencies of spinel-based construction ceramics incorporating simulated nickel-laden waste sludge were evaluated and the leaching behavior of products investigated. To simulate the process of immobilization, nickel oxide was mixed alternatively with γ-alumina, kaolinite, and hematite. These tailoring precursors are commonly used to prepare construction ceramics in the building industry. After sintering from 600 to 1480 °C at 3 h, the nickel aluminate spinel (NiAl2O4) and the nickel ferrite spinel (NiFe2O4) crystallized with the ferrite spinel formation commencing about 200-300 °C lower than for the aluminate spinel. All the precursors showed high nickel incorporation efficiencies when sintered at temperatures greater than 1250 °C. Prolonged leach tests (up to 26 days) of product phases were carried out using a pH 2.9 acetic acid solution, and the spinel products were invariably superior to nickel oxide for immobilization over longer leaching periods. The leaching behavior of NiAl2O4 was consistent with congruent dissolution without significant reprecipitation, but for NiFe2O4, ferric hydroxide precipitation was evident. The major leaching reaction of sintered kaolinite-based products was the dissolution of cristobalite rather than NiAl2O4. This study demonstrated the feasibility of transforming nickel-laden sludge into spinel phases with the use of readily available and inexpensive ceramic raw materials, and the successful reduction of metal mobility under acidic environments.

Original languageEnglish
Pages (from-to)5520-5526
Number of pages7
JournalEnvironmental Science and Technology
Volume40
Issue number17
DOIs
Publication statusPublished - Sept 1 2006
Externally publishedYes

ASJC Scopus Subject Areas

  • General Chemistry
  • Environmental Chemistry

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