C22B3/282

Methods for simultaneous leaching and extraction of precious metals

The present application relates to methods for the simultaneous leaching and extraction of precious metals. For example, the present application relates to methods of leaching and extracting gold and/or palladium from a substance comprising gold and/or palladium such as a gold- and/or palladium-containing ore in one step using a compound of Formula I:(I). ##STR00001##

Methods for selective leaching and extraction of precious metals in organic solvents

The present application relates to methods for leaching and extraction of precious metals. For example, the present application relates to methods of leaching gold, palladium and/or platinum from a substance comprising gold, palladium and/or platinum (such as a gold-containing ore or a platinum group metal (PGM) concentrate) using an organic solvent that is water-miscible or partially water-miscible.

DIGLYCOLAMIDE DERIVATIVES FOR SEPARATION AND RECOVERY OF RARE EARTH ELEMENTS FROM AQUEOUS SOLUTIONS
20220002229 · 2022-01-06 ·

Rare earth extractant compounds having the following structure:

##STR00001##

wherein R.sup.1, R.sup.2, R.sup.3, and R.sup.4 are independently selected from alkyl groups containing 1-30 carbon atoms and optionally containing an ether or thioether linkage connecting between carbon atoms, provided that the total carbon atoms in R.sup.1, R.sup.2, R.sup.3, and R.sup.4 is at least 12; R.sup.5 and R.sup.6 are independently selected from hydrogen atom and alkyl groups containing 1-3 carbon atoms; and provided that at least one of the conditions (i)-(iv) apply as follows: presence of a distal branched group in at least one of R.sup.1-R.sup.4 (condition i), asymmetry in R.sup.1-R.sup.4 (condition ii), presence of amine-containing ring (condition iii), or presence of lactam ring (condition iv). Also described are hydrophobic water-insoluble solutions containing at least one extractant compound of Formula (1), as well as method for extracting rare earth elements from aqueous solution by contacting the aqueous solution with the water-insoluble solution.

VANADIUM EXTRACTION FROM DISPARATE SHALE ORES

The invention provides for the orchestrated treatment of disparate fractions of a shale deposit to recover vanadium values, with distinct steps of beneficiation that together provide a combined vanadium-enriched concentrate amenable to subsequent combined steps of hydrometallurgical vanadium extraction.

Method for separating nickel and cobalt from a solution

A method for separating nickel and cobalt from a solution includes the steps of: obtaining a solution containing nickel and cobalt by acid leaching of a cathode material of a waste lithium-ion battery, adjusting the pH of the solution containing nickel and cobalt to 3.5 to 4.5, adding extractants for extraction to separate the nickel and the cobalt. The cobalt enters the organic phase, the nickel remains in the aqueous phase, and the extractants contain an acidic extractant and an alkaline extractant. The method for efficiently separating nickel and cobalt through extraction adopts a non-saponification extraction method without using NaOH as a saponifier, thereby avoiding the discharge of saponification wastewater. Under acidic conditions, the cobalt in an acidic leaching solution is effectively extracted and separated into the organic phase through synergistic action of the acidic extractant and the alkaline extractant, thereby realizing the separation of nickel from cobalt.

Lipophilic guanidinium compounds for removal of oxyanions from aqueous solutions

Methods for removing an oxyanion from an aqueous source containing said oxyanion, comprising contacting said aqueous source with an aqueous-insoluble hydrophobic solution containing an oxyanion extractant compound dissolved in an aqueous-insoluble hydrophobic solvent to result in formation of an oxyanion salt of said extractant compound and extraction of said oxyanion salt into said aqueous-insoluble hydrophobic solution, wherein said extraction results in an extraction affinity (D) of said oxyanion of at least 1, wherein D is the concentration ratio of said oxyanion in the organic phase divided by the concentration of said oxyanion in the aqueous phase; wherein said extractant compound has the following composition: ##STR00001##
wherein at least one of R.sup.1-R.sup.10 is or contains a hydrocarbon (R) group containing at least 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms.

Method of recovering metal compounds from solid oxide fuel cell scrap

A method of recovering metal compounds from solid oxide fuel cell scrap includes processing the solid oxide fuel cell scrap to form a powder, digesting the processed scrap, extracting lanthanum oxide and cerium oxide from a solution containing the digested processed scrap, extracting a zirconium compound from the solution after extracting the lanthanum oxide and cerium oxide, and extracting scandium compound from the solution extracting the zirconium compound from the solution.

METHOD FOR SEPARATING NICKEL AND COBALT FROM A SOLUTION

A method for separating nickel and cobalt from a solution includes the steps of: obtaining a solution containing nickel and cobalt by acid leaching of a cathode material of a waste lithium-ion battery, adjusting the pH of the solution containing nickel and cobalt to 3.5 to 4.5, adding extractants for extraction to separate the nickel and the cobalt. The cobalt enters the organic phase, the nickel remains in the aqueous phase, and the extractants contain an acidic extractant and an alkaline extractant. The method for efficiently separating nickel and cobalt through extraction adopts a non-saponification extraction method without using NaOH as a saponifier, thereby avoiding the discharge of saponification wastewater. Under acidic conditions, the cobalt in an acidic leaching solution is effectively extracted and separated into the organic phase through synergistic action of the acidic extractant and the alkaline extractant, thereby realizing the separation of nickel from cobalt.

Process for recycling chromium from waste water containing hexavalent chromium

A process for recovering chromium from hexavalent chromium-containing wastewater comprises the following steps: (1) extracting hexavalent chromium in wastewater to an organic phase by using an extracting agent, and separating hexavalent chromium from a water phase, so as to acquire a hexavalent chromium-loaded organic phase; (2) reducing the hexavalent chromium-loaded organic phase by using an aqueous solution of an organic reducing agent, reducing hexavalent chromium into trivalent chromium, reversely extracting trivalent chromium into the water phase, and separating the organic phase from the water phase to acquire a solution of the trivalent chromium and a renewable organic phase, wherein the organic reducing agent is one or a mixture of alcohols, aldehydes and carboxylic acids having the carbon atom number ranging 1 to 3; and (3) performing solvent evaporation on the solution of trivalent chromium, catalyzing, and recovering the trivalent chromium.

Processes for selective recovery of rare earth metals present in acidic aqueous phases resulting from the treatment of spent or scrapped permanent magnets

The invention relates to a hydrometallurgical process which makes it possible to selectively recover at least one heavy rare earth metal, i.e. a rare earth metal with an atomic number at least equal to 62, that is in an acidic aqueous phase resulting from the treatment of spent or scrapped permanent magnets. It also relates to a hydrometallurgical process which makes it possible to selectively recover, on the one hand, at least one heavy rare earth metal present in an acidic aqueous phase resulting from the treatment of spent or scrapped permanent magnets and, on the other hand, at least one light rare earth metal, i.e. a rare earth metal with an atomic number at most equal to 61, that is also in this acidic aqueous phase. The invention has in particular an application in the recycling of rare earth metals present in spent or scrapped permanent magnets of the type Neodymium-Iron-Boron (or NdFeB) and, in particular, dysprosium, praseodymium and neodymium, and also in the recycling of samarium present in spent or scrapped permanent magnets of the type samarium-cobalt (or SmCo).