Abstract: An improved process for the causticisation of Bayer liquors in an alumina refinery, the process including the steps of reacting lime with aluminate ions in a Bayer liquor within a primary reactor under controlled conditions of low to moderate temperature (between 70-80° C.) and agitation, to form substantially only a hydrocalumite species and hydroxyl ions; and a secondary reactor wherein the hydrocalumite species formed is subjected to heating in contact with a Bayer liquor under controlled conditions so as to cause the hydrocalumite species to react with the liquor to form calcium carbonate, aluminate ions and hydroxyl ions, whereby a causticised Bayer liquor is obtained and wherein the efficiency of lime utilization is substantially increased and/or alumina losses are minimized.

Abstract: A process for removing anionic impurities from a caustic aluminate solution having aqueous tetrahydroxy aluminate ions is described. A caustic aluminate solution is obtained such that anionic impurities are partially or substantially substituted into tetrahydroxy aluminate ions to form substituted aluminate ions. A suitable calcium compound, such as quicklime, is reacted in a conventional slaker (10) with a slaking solution, for example water, and stored in an agitated storage tank (12). The resulting slurry is pumped to a reaction vessel (14) where it is reacted with a caustic aluminate solution under appropriate conditions such that the calcium compound is converted into tricalcium aluminate (TCA) precipitate. Upon reaction substituted aluminate ions are substantially incorporated within the TCA precipitate to form a substituted TCA precipitate enabling the anionic impurities to be removed from the solution via the substituted TCA precipitate for disposal or recovery.

Abstract: A process for the removal and causticisation of sodium oxalate and/or sodium sulphate from a Bayer process liquor containing sodium carbonate and one or both of sodium oxalate and sodium sulphate in an alumina refinery is described. The process is based on the observation that to efficiently causticise sodium oxalate solutions, it is first necessary to remove the aluminate ion from solution, optionally with recovery of the aluminate ion in some later step. This is effected by removing aluminate ions from the Bayer liquor through the formation of a carbonate bearing hydrocalumite and/or sulpha-bearing hydrocalumite. The liquor may then be treated with sufficient lime to remove and causticise any residual carbonate ions and some or all of the oxalate ions present so that any reacted lime solids thus formed can be separated and safely disposed of.

Abstract: An improved process for the production of tricalcium aluminate (TCA) filter aid for use in an alumina refinery is described. Quicklime is slaked in a slaker tin using a suitable slaking solution to form a slaked lime slurry (10). A suitable surface-active agent is added to the slaking solution prior to slaking of the lime. Alternatively, the surface-active agents can be added to the slaked lime either during slaking or after slaking. The slaked lime slurry is then transferred to a stirred storage/transfer tank (12) before it is pumped to a lime aging tank (14). A concentrated Bayer liquor and steam are added to the tank (14) to provide a caustic aluminate solution that reacts with the slaked lime. Sufficient residence time is allowed in the lime aging tank (14) for the initial product of the reaction to “age” before use, forming relatively pure particles of the thermodynamically stable TCA.

Abstract: A process for the removal and causticisation of sodium oxalate and/or sodium sulphate from a Bayer process liquor containing sodium carbonate and one or both of sodium oxalate and sodium sulphate in an alumina refinery is described. The process is based on the observation that to efficiently causticise sodium oxalate solutions, it is first necessary to remove the aluminate ion from solution, optionally with recovery of the aluminate ion in some later step. This is effected by removing aluminate ions from the Bayer liquor through the formation of a carbonate-bearing hydrocalumite and/or sulphate-hearing hydrocalumite. The liquor may then be treated with sufficient lime to remove and causticise any residual carbonate ions and some or all of the oxalate ions present so that any reacted lime solids thus formed can be separated and safely disposed of.

Abstract: An improved process for the causticisation of Bayer liquors in an alumina refinery includes a first step of reacting lime with aluminate ions in a Bayer liquor within a primary reactor operated at low to moderate temperature to form a hydrocalumite species and hydroxyl ions. In a second step, the hydrocalumite species is heated in contact with a Bayer liquor, which either includes or is a different liquor than the Bayer liquor of the first step, under controlled conditions to cause the hydrocalumite species to react with the liquor to form calcium carbonate, aluminate ions and hydroxyl ions. The principal advantages of the improved process include very high lime utilisation efficiencies (in excess of 90%) and a substantially increased C/S ratio (in excess of 0.955), allowing higher plant caustic concentrations and improved productivity. The loss of alumina due to the formation of unwanted calcium aluminate species is also greatly reduced.

Abstract: A process for the removal of organic impurities in a Bayer process liquor in which wet and dry oxidation processes are linked together in a complementary way, such that the weaknesses of each individual organic removal process become a strength of the combined process. An organics-rich liquor stream is fed to a wet oxidation process to produce a first processed liquor which is depleted in organic compounds, but enriched in sodium carbonate and/or sodium oxalate. A feed slurry is fed to the dry oxidation process, typically including a liquor burner, where sodium compounds react to produce a discharge product. The first processed liquor and discharge product are directed into a leach tank, resulting in the formation of precipitated products including sodium carbonate and/or sodium oxalate. The precipitated products are separated from the leach tank and recycled in a mix tank providing the feed slurry to the liquor burner.