The use of an industry waste, brown coal fly ash collected from the Latrobe Valley, Victoria, Australia, has been tested for the post-combustion CO2 capture through indirect minersalization in acetic acid leachate. Upon the initial leaching, the majority of calcium and magnesium in fly ash were dissolved into solution, the carbonation potential of which was investigated subsequently through the use of a continuously stirred high-pressure autoclave reactor and the characterization of carbonation precipitates by various facilities. A large CO2 capture capacity of fly ash under mild conditions has been confirmed. The CO2 was fixed in both carbonate precipitates and water-soluble bicarbonate, and the conversion between these two species was achievable at approximately 60 degrees C and a CO2 partial pressure above 3 bar. The kinetic analysis confirmed a fast reaction rate for the carbonation of the brown coal ash-derived leachate at a global activation energy of 12.7 kJ/mol. It is much lower than that for natural minerals and is also very close to the potassium carbonate/piperazine system. The CO2 capture capacity of this system has also proven to reach maximum 264 kg CO2/tonne fly ash which is comparable to the natural minerals tested in the literature. As the fly ash is a valueless waste and requires no comminution prior to use, the technology developed here is highly efficient and energy-saving, the resulting carbonate products of which are invaluable for the use as additive to cement and in the paper and pulp industry. (C) 2012 Elsevier B.V. All rights reserved.