In alternative embodiments, the invention provides processes and methods for the recovery, removal or extracting of, and subsequent purification of uranium from a wet-process phosphoric acid using a continuous ion exchange processing approach, where the uranium is recovered from a phosphoric acid, or a phos-acid feedstock using either a dual or a single stage extraction methodology. In both cases an intermediate ammonium uranyl-tricarbonate solution is formed. In alternative embodiments, in the dual cycle approach, this solution is contacted in a second continuous ion exchange system with a strong anion exchange resin then subsequently recovered as an acidic uranyl solution that is further treated to produce an intermediate uranyl peroxide compound which is ultimately calcined to produce the final uranium oxide product. In alternative embodiments, in the single cycle case, the intermediate ammonium uranyl-tricarbonate solution is evaporated to decompose the ammonium carbonate and produce an intermediate uranium carbonate/oxide solid material. These solids are digested in an acid medium, and then processed in the same manner as the secondary regeneration solution from the dual cycle process to produce an intermediate uranyl peroxide that is calcined to produce a final uranium oxide product.

In alternative embodiments, the invention provides processes and methods for the recovery, removal or extracting of, and subsequent purification of uranium from a wet-process phosphoric acid using a continuous ion exchange processing approach, where the uranium is recovered from a phosphoric acid, or a phos-acid feedstock using either a dual or a single stage extraction methodology. In both cases an intermediate ammonium uranyl-tricarbonate solution is formed. In alternative embodiments, in the dual cycle approach, this solution is contacted in a second continuous ion exchange system with a strong anion exchange resin then subsequently recovered as an acidic uranyl solution that is further treated to produce an intermediate uranyl peroxide compound which is ultimately calcined to produce the final uranium oxide product. In alternative embodiments, in the single cycle case, the intermediate ammonium uranyl-tricarbonate solution is evaporated to decompose the ammonium carbonate and produce an intermediate uranium carbonate/oxide solid material. These solids are digested in an acid medium, and then processed in the same manner as the secondary regeneration solution from the dual cycle process to produce an intermediate uranyl peroxide that is calcined to produce a final uranium oxide product.

In alternative embodiments, the invention provides processes and methods for the recovery, removal or extracting of, and subsequent purification of uranium from a wet-process phosphoric acid using a continuous ion exchange processing approach, where the uranium is recovered from a phosphoric acid, or a phos-acid feedstock using either a dual or a single stage extraction methodology. In both cases an intermediate ammonium uranyl-tricarbonate solution is formed. In alternative embodiments, in the dual cycle approach, this solution is contacted in a second continuous ion exchange system with a strong anion exchange resin then subsequently recovered as an acidic uranyl solution that is further treated to produce an intermediate uranyl peroxide compound which is ultimately calcined to produce the final uranium oxide product. In alternative embodiments, in the single cycle case, the intermediate ammonium uranyl-tricarbonate solution is evaporated to decompose the ammonium carbonate and produce an intermediate uranium carbonate/oxide solid material. These solids are digested in an acid medium, and then processed in the same manner as the secondary regeneration solution from the dual cycle process to produce an intermediate uranyl peroxide that is calcined to produce a final uranium oxide product.

The present invention relates to a process and, more specifically, to a process for the removal of components from a starting material. Optionally, the process is used for the removal of contaminants from ion exchange regenerant material.

The present invention relates to a process and, more specifically, to a process for the removal of components from a starting material. Optionally, the process is used for the removal of contaminants from ion exchange regenerant material.

A novel apparatus for an ion exchange system is provided. The apparatus comprises a first column for housing a first fluidized bed through which particles are flowed countercurrently to an ion-containing fluid to yield ion-loaded particles, a second column through which the ion-loaded particles are flowed countercurrently to an eluent fluid to yield regenerated particles, and a transport section which transfers the regenerated particles for re-introduction into the first column to repeat the ion exchange cycle in a continuous manner. A continuous method of ion exchange is also provided.

A novel apparatus for an ion exchange system is provided. The apparatus comprises a first column for housing a first fluidized bed through which particles are flowed countercurrently to an ion-containing fluid to yield ion-loaded particles, a second column through which the ion-loaded particles are flowed countercurrently to an eluent fluid to yield regenerated particles, and a transport section which transfers the regenerated particles for re-introduction into the first column to repeat the ion exchange cycle in a continuous manner. A continuous method of ion exchange is also provided.

A fluid treatment apparatus comprising a tank containing a bed of at least one fluid treatment medium, a distributor plate separating the bed from an end portion of the tank, and an inert medium comprising amorphous particles having a harmonic mean diameter from 2.5 to 250 mm and a density from 0.57 to 0.998 cm.sup.3/g. The volume of the end portion containing inert medium is from 25 to 95% of the total volume of the end portion.

A fluid treatment apparatus comprising a tank containing a bed of at least one fluid treatment medium, a distributor plate separating the bed from an end portion of the tank, and an inert medium comprising amorphous particles having a harmonic mean diameter from 2.5 to 250 mm and a density from 0.57 to 0.998 cm.sup.3/g. The volume of the end portion containing inert medium is from 25 to 95% of the total volume of the end portion.

A method for harmless disposal and resource utilization of resin desorption liquid generated in the ion exchange process is provided. Resin desorption liquid is channeled into an electrolytic tank, which is arranged with an inlet and an outlet; the anode and the cathode within the electrolytic tank are separately connected to a stabilized power supply; both the direct and indirect oxidation process and occurred at the anode can decompose the organic pollutants in the desorption liquid; with necessary replenishment of fresh regeneration agent, the treated desorption liquid can exert excellent performance in regenerating saturated resin; the recycled use of resin desorption liquid is therefore realized, which consequently avoids unnecessary waste of regeneration agent and reduces the final yield of the desorption liquid. This method is characterized by being convenient in operation, without addition of extra reagents, without secondary pollution, and suitable for the desorption liquid with wide pH variations.