Neutralization of Acid Sulfate Solutions Using Bauxite Refinery Residues and Its Derivatives
Author(s) -
Sara J. Couperthwaite,
Dean W. Johnstone,
Graeme J. Millar,
Ray L. Frost
Publication year - 2012
Publication title -
industrial and engineering chemistry research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.878
H-Index - 221
eISSN - 1520-5045
pISSN - 0888-5885
DOI - 10.1021/ie301618p
Subject(s) - hydrotalcite , neutralization , chemistry , dissolution , sodalite , bauxite , sulfate , nuclear chemistry , leaching (pedology) , jarosite , mother liquor , inorganic chemistry , zeolite , crystallization , organic chemistry , soil water , catalysis , geology , antibody , immunology , biology , soil science
This investigation has shown that by transforming free caustic in red mud (RM) to Bayer hydrotalcite (during the seawater neutralization (SWN) process) enables a more controlled release mechanism for the neutralization of acid sulfate soils. The formation of hydrotalcite has been confirmed by X-ray diffraction (XRD) and differential thermalgravimetric analysis (DTG), while the dissolution of hydrotalcite and sodalite has been observed through XRD, DTG, pH plots, and ICP-OES. Coupling of all techniques enabled three neutralization mechanisms to be determined: (1) free alkali, (2) hydrotalcite dissolution, and (3) sodalite dissolution. The mechanisms are determined on the basis of ICP-OES and kinetic information. When the mass of RM or SWN-RM is greater than 0.08 g/50 mL, the pH of solution increases to a suitable value for plant life with aluminum leaching kept at a minimum. To obtain a neutralization pH greater than 6 in 10 min, the following ratio of bauxite residue (g) in 50 mL with a known iron sulfate (Fe2(SO4)3) concentration can be determined as follows: 0.04 g:50 mL:0.1 g/L of Fe2(SO4)3
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