Ligand Assisted Chromatography for Metal Ion Separation

Abstract

Presented herein is a ligand-assisted elution chromatography process for the separation of metal ions using a sorbent. In particular, the present invention discloses a process of two sets of column system in combination with two sets of eluting ligand solutions to prepare substantially pure rare earth elements, wherein the first set of column comprises strong acid cation exchange resins and the second set of chromatographic columns comprises hydrous polyvalent metal oxide selected from the group consisting of TiO2, ZrO2, or SnO2 and wherein ligand of said second ligand solution coordinates with said hydrous polyvalent metal oxide.

1 . A product of substantially pure rare earth element (REE) manufactured according to the process of
 a. dissolving a mixture containing REEs in a strong acid to result in a dissolved mixture of metal ions, including that of REEs;   b. capturing metal ions of REEs in a first set of chromatographic columns comprising strong acid cation exchange resins;   c. washing said first set of chromatographic columns with a salt solution to remove non-adsorbing metal ions;   d. eluting metal ions of REES from said first set of chromatographic columns with a first ligand solution to result in a solution of enriched metal ions of REEs;   e. loading said solution of enriched metal ions of REEs onto a second set of chromatographic columns; and   f. eluting bound metal ions of REEs stepwise from said second set of chromatographic columns using a second ligand solution to afford a substantially pure REE, wherein said second set of chromatographic columns comprising hydrous polyvalent metal oxide selected from the group consisting of TiO 2 , ZrO 2 , or SnO 2  and wherein ligand of said second ligand solution coordinates with said hydrous polyvalent metal oxide.   
     
     
         2 . The product of  claim 1 , wherein said salt solution is a sodium or ammonium salt solution with a counter ion selected from the group consisting of chloride (Cl − ), sulfate (SO 4   2− ), bisulfate (HSO 4   − ), and nitrate (NO 3   − ). 
     
     
         3 . The product of  claim 1 , wherein said first ligand is ethylenediaminetetraacetic acid (EDTA), pentetic acid (DTPA), 1,2-diaminocyclohexanetetraacetic acid (DCTA), N-(2-Hydroxyethyl) ethylenediamine-N,N′,N′-triacetic acid (HEDTA), iminodiacetic acid (IDA), citric acid, or any combination thereof. 
     
     
         4 . The product of  claim 1 , wherein said metal ions of REEs are eluted separately by using said first ligand solution with a linear or stepwise concentration gradient of said ligand. 
     
     
         5 . The product of  claim 1 , wherein said metal ions of REEs are eluted separately by using said first ligand solution with a linear or stepwise gradient of pH. 
     
     
         6 . The product of  claim 1 , wherein said second ligand solution is a solution of ethylenediaminetetraacetic acid (EDTA), pentetic acid (DTPA), 1,2-diaminocyclohexanetetraacetic acid (DCTA), N-(2-Hydroxyethyl) ethylenediamine-N,N′,N′-triacetic acid (HEDTA), iminodiacetic acid (IDA), citric acid, or any combination thereof. 
     
     
         7 . The product of  claim 1 , wherein metal ions of REEs are eluted separately by using said second ligand solution with a linear or stepwise concentration gradient of said ligand. 
     
     
         8 . The product of  claim 1 , wherein metal ions of REEs are eluted separately by using said second ligand solution with a linear or stepwise gradient of pH. 
     
     
         9 . The product of  claim 1 , wherein said strong acid compromises one or more acids selected from the group consisting of hydrochloric acid (HCl), sulfuric acid (H 2 SO 4 ), and nitric acid (HNO 3 ). 
     
     
         10 . A product of substantially pure praseodymium (Pr), neodymium (Nd), or samarium (Sm) of  claim 1 .