Process for the selective recovery of transition metals from organic residues

Patent metadata

Field	Value
Publication number	US-12392011-B2
Application number	US-201917413068-A
Country	US
Kind code	B2
Filing date	Dec 11, 2019
Priority date	Dec 11, 2018
Publication date	Aug 19, 2025
Grant date	Aug 19, 2025

Abstract

There is a process for the selective recovery of transition metals from an organic stream containing transition metals. The organic stream and possibly a first extractor if solid, are melted up to the liquid state. The extractor consists of an ionic liquid or a mixture of two or more ionic liquids and the ionic liquid contains an ammonium salt as cation and as anion an anion with chelating properties. A melted organic stream and a first extractor, optionally melted, are fed to a first liquid-liquid extraction unit working at a temperature of at least 150° C. where the liquid-liquid extraction is carried out obtaining a liquid mixture containing an ionic liquid, or a mixture of two or more ionic liquids, and metals. After extraction, the liquid mixture is cooled at a temperature between 0° C. and 70° C. and becomes biphasic; then the cooled mixture is sent to a first separation unit, to separate a liquid phase that contains ionic liquids and metals, and a metal-depleted solid phase. After the first separation, the separated metal-depleted solid phase is optionally sent to a washing unit to which a solvent is fed, so as to eliminate the residual ionic liquid by transferring it into the solvent and obtaining a metal-depleted solid phase. Then the separate liquid phase containing ionic liquids and metals is sent into a liquid-liquid precipitation and separation unit, adding a counter-solvent, thereby obtaining a solid phase containing the metals and a liquid stream containing counter-solvent and ionic liquids.

First claim

The invention claimed is:

1. Process for the selective recovery of transition metals from an organic stream having a boiling point higher than or equal to 340° C. and containing transition metals which comprises the following steps:
a. melting up to the liquid state said organic stream and possibly a first extractor if solid, where said first extractor consists of an ionic liquid or a mixture of two or more ionic liquids, wherein said ionic liquid contains a quaternary ammonium salt or a quaternary phosphonium salt as cation and an anion with chelating properties as anion;
b. feeding to a first liquid-liquid extraction unit working at a temperature of at least 150° C. said molten organic stream and said first extractor, optionally melted, and carrying out the liquid-liquid extraction, obtaining a liquid mixture containing an ionic liquid, or a mixture of two or more ionic liquids, and the metals;
c. after extraction, cooling at a temperature comprised between 0° C. (zero degrees centigrade) and 70° C. said liquid mixture, which after cooling is biphasic, and subsequently sending the biphasic mixture to a first liquid-solid separation unit, to separate a liquid phase that contains ionic liquids and metals, and a metal-depleted solid phase;
d. after the first separation, the separated metal-depleted solid phase is optionally sent to a washing unit to which a solvent is fed, so as to eliminate the residual ionic liquid by keeping it into the solvent and obtaining a washed metal-depleted solid;
e. sending the separate liquid phase containing ionic liquids and metals into a liquid-solid precipitation and separation unit and adding a counter-solvent, thereby obtaining a solid phase containing the metals and a liquid flow containing counter-solvent and ionic liquids,
wherein the anion is selected from salicylate, thiosalicylate, acetate, citrate, oxalate, malonate, dicyanoamide, and glutarate, and
wherein in the extraction step, in addition to the ionic liquid, an extracting agent selected from the group consisting of thiocarbazones, thiocarbamides, mercaptobenzenes and aromatic carboxylic acids containing a thiol group is used.

2. Process according to claim 1 , wherein the counter-solvent containing residual ionic liquids is further recovered in an evaporation unit forming counter-solvent and metal-free ionic liquid which is recycled to the first extraction step.

3. Process according to claim 1 , wherein the cation is selected from imidazolium, pyridinium, tetra alkylguanidinium, uronium, thiouronium; or a quaternary phosphonium salt.

4. Process according to claim 1 , wherein the ionic liquid is selected from the group consisting of (1-butyl-3 methylimidazolium)dicyanoamide, (1-ethyl-3 methylimidazolium)salicylate, and (1-ethyl-3 methylimidazolium)thiosalicylate.

5. Process according to claim 1 , wherein the separation takes place by filtration or centrifugation.

6. Process according to claim 1 , wherein the weight ratio between said organic stream and the ionic liquid, or mixture of ionic liquids, ranges from 1:10 to 1:0.5.

7. Process according to claim 1 , wherein the solvent used in the washing step is selected from methanol and tetrahydrofuran.

8. Process according to claim 1 , wherein the counter-solvent used in the liquid-liquid extraction steps subsequent to the first one is selected from water, ethanol, propanol.

9. Process according to claim 1 , wherein the operating temperature at which the first extraction is carried out ranges from 150° C. to 250° C.

10. Process according to claim 1 , wherein the operating temperature at which the first separation is carried out ranges from 0° C. to 70° C.

11. Process according to claim 1 , wherein the extraction and separation steps are at pressure lower than or equal to 15 atm.

12. Process according to claim 1 , wherein the extraction time during the extraction step ranges from 4 hours to 48 hours.

13. Process according to claim 1 , wherein said organic stream is produced in refinery processes and/or in hydro-conversion processes of heavy hydrocarbons.

14. Process according to claim 13 , wherein said organic stream is produced in the “Eni Slurry Technology process” for the hydro-conversion of heavy oil products comprising the steps of:
supplying to a hydro-conversion section in slurry phase a molybdenum-containing catalyst precursor, heavy oil products and a hydrogen-containing stream;
conducting a hydro-conversion reaction producing a reaction effluent which is subsequently separated into a vapour phase and a slurry phase;
subsequently sending the separate vapour phase to a gas treatment section with the function of separating a liquid fraction from the gas containing hydrogen and hydrocarbon gases having from 1 to 4 carbon atoms; said liquid fraction comprising naphtha, atmospheric gas oil (AGO), vacuum gas oil (VGO);
subsequently sending the slurry phase to a separation section which has the function of separating the Vacuum Gas Oil (VGO), Heavy Vacuum Gas Oil (HVGO), Light Vacuum Gas Oil (LVGO), Atmospheric Gas Oil (AGO), from a stream of heavy organic products which contains asphaltenes, unconverted feed, catalyst and solid formed during the hydro-conversion reaction;
recycling a part of said heavy organic products to the reaction section and forming a purge stream with the remainder.

15. Process according to claim 13 , wherein said organic stream is a purge or a cake produced in a hydro-conversion process of heavy hydrocarbons, wherein said purge is an organic stream in slurry phase characterized by the presence of quantities of asphaltenes higher than or equal to 5% by weight and by the presence of solids content higher than or equal to 5% by weight, said solids containing carbonaceous residues, metallic compounds containing sulphides of transition metals selected from the group consisting of molybdenum, iron, nickel and vanadium, and having sub-millimetric dimensions; and wherein said cake is a solid material at room temperature with a softening point, defined as the temperature at which the solid cake becomes soft, between 80° C. and 100° C., and a degree of penetration, measured according to the ASTM-D5-06 method, from 2 dmm to 5 dmm; the cake being grindable and consequently transportable at temperatures ranging from 50° C. to 60° C. without thermostatic control.

16. Process according to claim 1 , wherein the transition metals which are selectively extracted are molybdenum and one or more selected from the group consisting of scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, yttrium, zirconium, niobium, ruthenium, rhodium, palladium, silver, cadmium, lanthanum, hafnium, thallium, tungsten, rhenium, osmium, iridium, platinum, gold and mercury.

17. Process according to claim 16 , wherein the one or more transition metals which are selectively extracted are selected from the group consisting of vanadium, nickel, cobalt, chromium, manganese and iron.

Assignees

• Eni Spa

Inventors

• Guidetti Stefania
• De Angelis Alberto Renato

Classifications

• C22B34/345

  from spent catalysts · CPC title

• C22B34/225

  from spent catalysts · CPC title

• C10G67/04

  including solvent extraction as the refining step in the absence of hydrogen · CPC title

• B01D11/0492 Primary

  Applications, solvents used · CPC title

• B01D11/0488

  Flow sheets · CPC title