阅读说明：本技术 苛性转化方法 (Caustic conversion process ) 是由 A·纳皮耶 C·格里菲思 于 2019-07-24 设计创作，主要内容包括：本发明涉及从未煅烧的含锂硅酸盐中提取锂并从中回收锂盐的方法。在高压釜中加热未煅烧的含锂硅酸盐和苛性溶液的浆液以提供富锂方钠石相。富锂方钠石相用稀酸浸出以产生富锂母液。本发明还描述了处理富锂母液以回收诸如磷酸锂、碳酸锂、硫酸锂或氢氧化锂等锂盐的各种后续工艺。(The present invention relates to a process for extracting lithium from an uncalcined lithium-containing silicate and recovering the lithium salt therefrom. The slurry of uncalcined lithium-containing silicate and caustic solution is heated in an autoclave to provide a lithium-rich sodalite phase. The lithium-rich sodalite phase is leached with dilute acid to produce a lithium-rich mother liquor. Various subsequent processes for treating the lithium-rich mother liquor to recover lithium salts such as lithium phosphate, lithium carbonate, lithium sulfate or lithium hydroxide are also described.)

1. A process for extracting lithium from an uncalcined lithium-containing silicate comprising the steps of:

a) heating a slurry of uncalcined lithium-containing silicate and caustic solution in an autoclave to produce a lithium-rich sodalite phase; and

b) the lithium-rich sodalite phase is leached with dilute acid to produce a lithium-rich mother liquor.

2. A process for recovering lithium salts from uncalcined lithium-containing silicates comprising the steps of:

a) heating a slurry of uncalcined lithium-containing silicate and caustic solution in an autoclave to produce a lithium-rich sodalite phase;

b) leaching the lithium-rich sodalite phase with dilute acid to produce a lithium-rich mother liquor; and

c) the lithium-rich mother liquor is treated to recover the lithium salt.

3. A process as claimed in claim 1 or claim 2, wherein the solids content of the slurry may be 25 wt% or less.

4. A process as claimed in any one of claims 1 to 3, wherein the caustic solution comprises 30% to 60% w/w NaOH or 30% to 60% w/w KOH.

5. A process according to any one of claims 1 to 4 wherein the slurry is heated in an autoclave to a temperature in the range 200 ℃ to 350 ℃.

6. A process according to any one of the preceding claims wherein the slurry is heated for a period of from 1 to 6 hours.

7. The process of any one of the preceding claims, wherein after heating the slurry to produce the lithium-rich sodalite phase, the process further comprises diluting the slurry with water.

8. The method of claim 7, wherein the slurry is diluted to 10-30% w/w NaOH or 10-30% w/w KOH.

9. The process of claim 7 or 8 wherein the lithium-rich sodalite phase is separated from the diluted slurry.

10. The process of claim 9 wherein the separated lithium-rich sodalite phase is washed one or more times to remove residual dilute caustic solution.

11. The process of claim 9, wherein the separated dilute caustic solution is treated with lime to produce insoluble calcium aluminate and calcium silicate.

12. The process of claim 10, wherein one or more of the scrubbing solutions are combined and treated with lime to produce insoluble calcium aluminate and calcium silicate and regenerated caustic solution for recycle to step a).

13. The process of claim 9 or 10 wherein the separated dilute caustic solution and one or more washings are combined and treated with lime to produce insoluble calcium aluminate and calcium silicate.

14. A method as claimed in any one of claims 11 to 13, wherein the lime may comprise a lime slurry comprising 5 to 50% by weight lime.

15. The process according to claim 11 or 13, wherein insoluble calcium aluminate and calcium silicate are separated from the slurry.

16. The process of claim 15 wherein the caustic concentration of the separated dilute caustic solution and/or the combined wash liquor is increased and said solution and/or wash liquor is recycled for use as the caustic solution in step a) of the process.

17. The method of claim 16, wherein the concentrated caustic solution and/or the combined wash solution comprises 30-60 wt% NaOH or KOH and 0.1-4g/L Li.

18. The method of claim 16 or 17, wherein increasing the concentration of the caustic solution comprises evaporating the caustic solution at a temperature of 80-150 ℃ under atmospheric or reduced pressure.

19. The process of any one of the preceding claims, wherein leaching the lithium-rich sodalite phase with the dilute acid is carried out at a temperature of 20-80 ℃.

20. A method as claimed in any one of the preceding claims, wherein the leaching step is carried out for 30min to 80 hours.

21. The process of any of the preceding claims, wherein the dilute acid comprises HCl or H₂SO₄。

22. The process according to any of the preceding claims, wherein the dilute acid has a pH of 2-6.

23. The process of any one of the preceding claims, wherein the slurry of the lithiated sodalite phase and the dilute acid has a solids content of 50 wt% or less.

24. The process of any one of the preceding claims, wherein the lithium extraction from the lithium-rich sodalite phase to PLS is > 90%.

25. The process of any one of the preceding claims, wherein the lithium-rich mother liquor comprises 5-25g/L Li.

26. The method of any of claims 2-25, wherein the lithium salt comprises lithium carbonate, lithium hydroxide, lithium phosphate, or lithium sulfate.

27. The process of any one of claims 2-26, wherein prior to treating the lithium-rich mother liquor to recover the lithium salt, the process further comprises removing impurities from the lithium-rich mother liquor.

28. The process of claim 27, wherein the step of removing impurities from the lithium-rich mother liquor comprises bringing the lithium-rich mother liquor to a pH >10 by adding a base to the lithium-rich mother liquor and separating the precipitate containing the impurities by filtration.

29. The process as set forth in claim 27 or 28 further comprising softening the lithium-rich mother liquor by reducing the calcium content of the lithium-rich mother liquor to less than 25ppm after removing impurities from the lithium-rich mother liquor.

30. The method of claim 29, wherein the step of softening comprises adding an alkali metal carbonate or an alkali metal phosphate to the lithium-rich mother liquor to produce a calcium precipitate comprising calcium carbonate or apatite, and separating the calcium precipitate.

31. The process as set forth in any one of claims 26 to 30 wherein treating the lithium-rich mother liquor to recover lithium carbonate comprises contacting the lithium-rich mother liquor with carbon dioxide to produce lithium carbonate solids and a lithium-depleted solution.

32. The method of any one of claims 26-28, wherein processing the lithium-rich mother liquor to recover lithium carbonate comprises adding carbonate to the lithium-rich mother liquor to produce lithium carbonate solids and a lithium-depleted solution.

33. The method of any one of claims 26-28, wherein processing the lithium-rich mother liquor to recover lithium phosphate comprises adding phosphate to the lithium-rich mother liquor to produce lithium phosphate solids and a lithium-depleted solution.

34. The process of any one of claims 26-28, wherein processing the lithium-rich mother liquor to recover lithium sulfate comprises evaporating the lithium-rich mother liquor to produce lithium sulfate solids and a lithium-depleted solution.

35. The method of any one of claims 26-28, wherein processing the lithium-rich mother liquor to recover lithium hydroxide comprises:

i) adding sodium hydroxide solution into the lithium-rich mother liquor to ensure that the pH value is more than 10:

ii) cooling said lithium rich mother liquor from step i) to <10 ℃ to crystallize salt cake therefrom;

iii) separating salt cake from said lithium rich mother liquor from step ii); and

iv) concentrating said lithium-rich mother liquor from step iii) to 50% to 90% of its volume by evaporation, allowing lithium hydroxide solids to crystallize from said concentrated lithium-rich mother liquor.

36. The method of claim 35, wherein lithium hydroxide solids are separated from the concentrated lithium-rich mother liquor leaving a lithium-depleted solution.

37. The method of claim 36, wherein the lithium-depleted solution is recycled to step i) or the step of removing impurities.

38. A process for recovering lithium hydroxide from lithium-containing silicates comprising the steps of:

a) heating a slurry comprising a lithium silicate and a caustic solution in an autoclave to produce a lithium-rich sodalite phase;

b) leaching the lithium-rich sodalite phase with a dilute sulfuric acid solution to produce a lithium-rich mother liquor;

c) treating the lithium-rich mother liquor to remove impurities;

d) concentrating the treated lithium-rich mother liquor to increase the concentration of sodium sulfate and lithium;

e) crystallizing at low temperature to remove sodium sulfate; and

f) crystallizing and recovering the lithium hydroxide.

39. A method of recovering lithium phosphate from lithium-containing silicates, comprising the steps of:

a) heating a slurry comprising a lithium silicate and a caustic solution in an autoclave to produce a lithium-rich sodalite phase;

b) leaching the lithium-rich sodalite phase with an acid to produce a lithium-rich mother liquor;

c) treating the lithium-rich mother liquor to remove impurities; and

d) a phosphorus-containing compound is added to the lithium-rich mother liquor to produce lithium phosphate solids and a lean solution free of phosphorus compounds.

40. The process of claim 39 wherein the process further comprises separating lithium phosphate solids from the lean solution free of phosphorus-containing compounds, adding an alkali metal hydroxide to the lean solution free of phosphorus-containing compounds, and recycling the lean solution free of phosphorus-containing compounds to step b).

Technical Field

The present invention relates to a method for recovering lithium from a lithium-containing material. In particular, the invention relates to a method for recovering lithium phosphate, lithium carbonate or lithium hydroxide from lithium-containing silicate.

Background

Currently, lithium is supplied globally from salt water or hard rock deposits.

In the former, lithium is concentrated by solar evaporation to a soluble lithium salt. Lithium produced from brine is generally low grade, and while capital investment for production from brine is high, operating costs are low.

In the case of hard rock deposits, conventional mining and beneficiation techniques are used to produce high grade alpha-spodumene (alpha-spodumene) concentrates. Lithium chemicals of technical grade, battery grade (99.5%) or high purity (> 99.9%) lithium carbonate can be obtained from various air and lime roasting processes.

The air roasting process involves first blasting (>1000 ℃) to convert alpha-spodumene to the more reactive beta polymorph, then sulfation roasting with sulfuric acid at 250 ℃, and then aqueous leaching of the acid roasting residue at 90 ℃ to extract lithium into solution. This method is widely recognized as a "conventional" method of extracting lithium from spodumene. On the other hand, the lime roasting process relies on roasting spodumene and lime at temperatures >1000 ℃, followed by water leaching of the roasted mass (clinker) to extract lithium into solution. Other methods of extracting lithium from alpha-spodumene by pressure leaching with soda or chloridizing roasting have also been proposed.

All of these processes involve an energy intensive pre-high temperature calcination step (i.e., calcination). It has been demonstrated that the high energy sources associated with roasting (calcining) low grade lithium concentrates face cost challenges.

Therefore, there is a need to develop an alternative or improved process to recover lithium from silicate materials that avoids energy intensive processing steps such as calcination (calcining).

It will be understood that, if any prior art publication is referred to herein, this reference does not constitute an admission that the publication forms part of the common general knowledge in the art in australia or in any other country.

Disclosure of Invention

The present invention provides a method for extracting lithium values from lithium-containing materials, particularly lithium-containing silicates such as spodumene, in the absence of a preliminary firing step to convert alpha-spodumene to beta-spodumene. The invention also provides a method for recovering the lithium value of lithium carbonate or lithium phosphate from lithium-containing materials, particularly lithium-containing silicates.

According to a first aspect of the present invention there is provided a process for extracting lithium from an uncalcined lithium-containing silicate comprising the steps of:

a) heating a slurry of uncalcined lithium-containing silicate and caustic solution in an autoclave to produce a lithium-rich sodalite phase; and

b) the lithium-rich sodalite phase is leached with dilute acid to produce a lithium-rich mother liquor.

According to a second aspect of the present invention, there is provided a process for recovering lithium salts from uncalcined lithium-containing silicates, comprising the steps of:

a) heating a slurry of uncalcined lithium-containing silicate and caustic solution in an autoclave to produce a lithium-rich sodalite phase;

b) leaching the lithium-rich sodalite phase with dilute acid to produce a lithium-rich mother liquor; and

c) treating said mother liquor to recover the lithium salt.

In one embodiment, the lithium salt may be lithium carbonate, lithium hydroxide, lithium phosphate, or lithium sulfate.

In one embodiment, the solids content of the slurry may be 25 wt% or less.

In another embodiment, the caustic solution comprises 30% to 60% w/w NaOH. In another embodiment, the caustic solution comprises 30% to 60% w/w KOH.

In one embodiment, the slurry is heated in an autoclave to 200 ℃ to 350 ℃, particularly 250 ℃ to 290 ℃. The heating step may be carried out for 1 to 6 hours, in particular 2 to 4 hours.

In various embodiments, after heating the slurry to produce the lithium-rich sodalite phase, the method further comprises diluting the slurry with water at a higher temperature, particularly 80 ℃ or higher. The slurry may be diluted to 10-30% w/w NaOH or 10-30% w/w KOH. The lithium-rich sodalite phase may then be separated from the diluted slurry. It will be appreciated that the separated sodalite-rich phase may be washed one or more times to remove residual dilute caustic solution.

In one embodiment, after separation of the lithium-rich sodalite phase from the diluted slurry, the separated dilute caustic solution may be treated with a lime slurry to produce insoluble calcium aluminate and calcium silicate, and the regenerated caustic solution may be recycled to step a). The lime slurry may be 5-50 wt% lime, especially 30 wt% lime. Subsequently, insoluble calcium aluminate and calcium silicate can be separated from the slurry.

In another embodiment, the aforementioned wash liquor or wash liquors may be treated with a lime slurry to produce insoluble calcium aluminate and calcium silicate. The lime slurry may be 5-50 wt% lime, especially 30 wt% lime. Insoluble calcium aluminate and calcium silicate can be separated from the slurry.

In another embodiment, the separated dilute caustic solution and the aforementioned wash liquor or wash liquors may be combined and treated with a lime slurry to produce insoluble calcium aluminate and calcium silicate. The lime slurry may be 5-50 wt% lime, especially 30 wt% lime. Insoluble calcium aluminate and calcium silicate can be separated from the slurry.

In some embodiments, the separated and/or combined caustic solution from which the insoluble calcium aluminate and calcium silicate have been separated may be concentrated and/or recycled for use as the caustic solution in process step a). In some embodiments, the concentrated caustic solution may include 30 to 60 wt% NaOH or KOH, particularly 30 to 40 wt% NaOH or KOH, and 0.1 to 4g/L Li.

The caustic strength of the caustic solution may include evaporating the remaining liquid for a time sufficient to increase the caustic strength to the saturation limit of the caustic solution used. In some embodiments, evaporation may be conducted at atmospheric or reduced pressure. In some embodiments, the temperature of evaporation may be 80-150 ℃.

In various embodiments, leaching the lithium-rich sodalite phase with dilute acid is performed at a temperature of 20 to 90 ℃, particularly 60 to 80 ℃. The time of the leaching step may be 30 minutes to 24 hours, in particular 6 to 12 hours.

In one embodiment, the dilute acid comprises HCl or H₂SO₄. The dilute acid may have a pH of from 2 to 6, especially a pH of 4.

In one embodiment, the solids content of the slurry of the lithium-rich sodalite phase and the dilute acid may be less than or equal to 50 wt%.

In various embodiments, the lithium extraction rate from the lithium-rich sodalite phase to the lithium-rich mother liquor may be > 90%, particularly > 95%. In some embodiments, the lithium-rich mother liquor comprises 5 to 25g/L Li, especially 10 to 15g/L Li. In some embodiments, in step b), at least a portion of the lithium-rich mother liquor may be recovered for slurrying the lithium-rich sodalite phase to increase the lithium content of the resulting lithium-rich mother liquor.

In various embodiments, the method further comprises removing impurities from the lithium-rich mother liquor prior to treating the lithium-rich mother liquor to recover the lithium salt. In some embodiments, the step of removing impurities from the lithium-rich mother liquor comprises adding a base to the lithium-rich mother liquor such that the lithium-rich mother liquor has a pH > 10. Suitable bases include, but are not limited to, sodium hydroxide, potassium hydroxide, lithium hydroxide, lime, ammonia, or a combination of two or more of the foregoing. It will be appreciated that the impurities may be separated by filtration.

In some embodiments, after removing impurities from the lithium-rich mother liquor, the process may further comprise softening the mother liquor by reducing the calcium content of the mother liquor to less than 25 ppm. In some embodiments, the step of softening may comprise adding potassium carbonate or potassium phosphate to the lithium-containing solution to produce a calcium precipitate comprising calcium carbonate or apatite. In other embodiments, the softening step may comprise adding an alkali metal phosphate (e.g., sodium phosphate) to the mother liquor to produce a calcium precipitate comprising apatite.

In some embodiments, after removing impurities from the lithium-rich mother liquor, the method can further comprise softening the lithium-rich mother liquor by reducing its calcium content to less than 25 ppm. In some embodiments, the softening step may include adding potassium carbonate or potassium phosphate to the lithium-containing solution to produce a calcium precipitate comprising calcium carbonate or apatite. In other embodiments, the softening step may comprise adding an alkali metal phosphate, such as sodium phosphate, to the lithium-rich mother liquor to produce a calcium precipitate comprising apatite.

In one embodiment, treating the lithium-rich mother liquor to recover lithium carbonate includes contacting the lithium-rich mother liquor with carbon dioxide to produce lithium carbonate solids and a lithium-depleted solution.

In another embodiment, treating the lithium-rich mother liquor to recover lithium carbonate includes adding carbonate to the lithium-rich mother liquor to produce lithium carbonate solids and a lithium-depleted solution. Suitable carbonates include, but are not limited to, ammonium carbonate, sodium carbonate, potassium carbonate, or mixtures thereof.

The lithium carbonate solids may be separated from the lithium-depleted solution. In one embodiment, the lithium-depleted solution may be recycled to the leaching step.

In another embodiment, treating the lithium-rich mother liquor to recover lithium phosphate comprises adding a phosphorus-containing compound (phosphate) to the lithium-rich mother liquor to produce lithium phosphate solids and a lean solution. The phosphorus-containing compound may be added as a solid or as an aqueous solution. The phosphorus-containing compound may be selected from phosphoric acid, potassium phosphate, sodium phosphate, or a combination thereof.

In some embodiments, the method may further comprise recovering the phosphorus-containing compound from the separated solution as tricalcium phosphate and/or apatite. The tricalcium phosphate and/or apatite may be separated from the softening liquid. In these embodiments, recovering the phosphorus-containing compound as tricalcium phosphate and/or apatite from the separated solution may include adding calcium hydroxide to the separated solution.

In another embodiment, the dilute acidic solution comprises sulfuric acid and treating the lithium-rich mother liquor to recover lithium sulfate comprises evaporating the lithium-rich mother liquor to recover lithium sulfate.

In another embodiment, treating the lithium-rich mother liquor to recover lithium hydroxide comprises:

i) adding sodium hydroxide solution into the lithium-rich mother liquor to ensure that the pH value is more than 10:

ii) cooling said PLS from step i) to <10 ℃ to crystallize salt cake (Glauber salt) therefrom;

iii) separating mirabilite from said lithium-rich mother liquor from step ii); and

iv) concentrating said lithium-rich mother liquor from step iii) to 50% to 90% of its volume by evaporation, and allowing the concentrated lithium-rich mother liquor to crystallize lithium hydroxide solids.

In some embodiments, the evaporation may be carried out at atmospheric or reduced pressure. In some embodiments, the temperature of evaporation may be from 80 ℃ to 150 ℃.

Lithium hydroxide solids can be separated from the concentrated lithium-rich mother liquor to leave a lithium-depleted solution. In one embodiment, the lithium-depleted solution may be recycled to step i) or the step of removing impurities.

According to a third aspect of the present invention there is provided a process for recovering lithium hydroxide from lithium-containing silicates, comprising the steps of:

a) heating a slurry comprising a lithium silicate and a caustic solution in an autoclave to produce a lithium-rich sodalite phase;

b) leaching the lithium-rich sodalite phase with a dilute sulfuric acid solution to produce a lithium-rich mother liquor;

c) treating the lithium-rich mother liquor to remove impurities;

d) concentrating the treated lithium-rich mother liquor to increase the concentration of sodium sulfate and lithium;

e) removing sodium sulfate by crystallization at low temperature; and

f) crystallizing and recovering the lithium hydroxide.

According to a fourth aspect of the present invention, there is provided a method of recovering lithium phosphate from a lithium-containing silicate, comprising the steps of:

a) heating a slurry comprising a lithium silicate and a caustic solution in an autoclave to produce a lithium-rich sodalite phase;

b) leaching the lithium-rich sodalite phase with an acid to produce a lithium-rich mother liquor;

c) treating the lithium-rich mother liquor to remove impurities; and

d) a phosphorus-containing compound is added to the lithium-rich mother liquor to produce lithium phosphate solids and a lean solution free of phosphorus compounds.

In one embodiment, the process further comprises separating lithium phosphate solids from the lean solution of the phosphorus-free compound, adding an alkali metal hydroxide to the lean solution of the phosphorus-free compound, and recycling the lean solution of the phosphorus-free compound to step b).

Drawings

Although any other form may fall within the scope of the method described in the summary, specific embodiments will now be described, by way of example only, with reference to the accompanying drawings, in which:

FIG. 1 is a flow diagram depicting a process for recovering lithium phosphate from lithium-containing silicates.

Detailed Description

The present invention is described in the following various non-limiting examples, which relate to a process for recovering lithium values, particularly lithium carbonate, from lithium-containing materials, particularly uncalcined lithium-containing silicates.

General terms

Throughout this specification, unless specifically stated otherwise or the context requires otherwise, reference to a single step, composition of matter, group of steps or group of matter shall include one or more (i.e., one or more) of such steps, compositions of matter, groups of steps or group of matter. Thus, as used herein, the singular forms "a," "an," and "the" include plural aspects unless the context clearly dictates otherwise. For example, reference to "a" includes one and two or more; reference to "a" includes one and two or more; reference to "the" includes one and two or more, and so on.

Unless specifically stated otherwise, each embodiment of the invention described herein will apply, mutatis mutandis, to each other embodiment. The scope of the present disclosure is not limited to the particular embodiments described herein, which are intended to be illustrative only. Functionally equivalent products, compositions and methods are clearly within the scope of the disclosure described herein.

The term "and/or" (e.g., "X and/or Y") should be understood as "X and Y" or "X or Y" and should be taken as providing express support for both meanings or either meaning.

In this specification, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

It will be clearly understood that, although a number of prior art publications are referred to herein, this reference does not constitute an admission that any of these documents form part of the common general knowledge in the art, in australia or in any other country.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

Specific terminology

As used herein, the term "lithium-containing silicate" refers to a concentrate (concentrate), ore (ore), or tailings (tails) derived from one or more lithium-containing value silicate minerals. Exemplary lithium-containing silicates include, but are not limited to, giardiate (jadarite), spodumene (spodumene) and other pyroxenes (pyroxene), livinite (trilithionite), petalite (petalite), and other lithium-containing silicates from the nepheline (nepheline) mineral group, lithionite (holmqristite) and other lithium-containing silicates from the amphibole (amphilite) group, lepidolite (lepidolite), lepidolite (zinwaldeie), lithium tourmaline (baelite), and other tourmaline (tourmaline), chlorite, smectite, lithium-containing mica, and lithium-containing clays. The process described herein is particularly suitable for recovering lithium from alpha spodumene or petalite. Several metals (such as Mn, Rb and Cs) and other minerals (such as quartz (quartz), albite (albite), feldspar (feldspar), topaz (topaz) and beryl) may also be associated with these lithium minerals. Thus, the term "lithium-containing silicate" includes high grade ores and concentrates as well as medium to low grade ores, concentrates and blends thereof.

Calcination is a thermal process in which the solid is heated to high temperatures (i.e., >500 ℃) in the absence or controlled amount of air or oxygen, typically resulting in decomposition of the solid into carbon dioxide, water of crystallization, or volatiles, or causing a phase change, such as the conversion of alpha-spodumene to beta-spodumene. Such heat treatment processes may be carried out in furnaces or reactors, such as shaft furnaces, rotary kilns, multi-stage furnaces and fluidized bed reactors. As used herein, the term "uncalcined" refers to a solid that has not undergone calcination. In particular, the term "uncalcined lithium silicate" when used with respect to lithium silicate refers to lithium silicate that has not undergone calcination or any other heat treatment capable of causing a phase change.

Reference throughout this specification to "g/kg" or "kg/t" means the mass of a substance per kilogram or ton of lithium-containing material.

The term "lithium-rich sodalite phase" refers to a phase having the general formula M₈(Al₆Si₆O₂₄)(OH)₂The sodalite (OH form) of (a) is a crystalline structure-equivalent aluminosilicate phase in which cations ('M') and hydroxide (OH) reside in aluminosilicate cages in the unit cell. As used herein, "a" lithium-rich sodalite phase "refers to a phase in which Li at least partially replaces Na or K in the aluminosilicate cage.

The term "apatite" as used herein refers to the general formula Ca₅(PO₄)₃(F, Cl, OH) (repeating units), and may include hydroxyapatite, fluoroapatite, green apatite, or a mixture thereof.

Method for extracting lithium values

As described herein, the methods for extracting lithium values from lithium-containing materials are particularly applicable to lithium-containing silicates, particularly uncalcined lithium-containing silicates, such as α -spodumene and petalite. The lithium extraction rate achieved by this method can be > 85%, > 90%, > 95%, or even > 98%.

The uncalcined lithium-containing silicate may be milled to P prior to performing the methods described herein₁₀₀<160 μm. In certain embodiments, the uncalcined lithium-containing silicate may have a P of 20 to 160 μm, 40 to 100 μm, or 40 to 50 μm₈₀And (4) the particle size. The uncalcined lithium-containing silicate may be ground to the desired particle size in a dry or wet grinding process by conventional techniques well known in the art.

Referring to the figure, the lithium values can be extracted from the uncalcined lithium-containing silicate by heating (100) a slurry of the uncalcined lithium-containing silicate and a caustic solution in an autoclave to produce a lithium-rich sodalite phase.

The slurry may have a solids content of 25 wt% or less, in particular 20 wt%.

The term "caustic solution" as used herein generally refers to an aqueous sodium hydroxide solution, but may also include aqueous hydroxide solutions having one or more types of counter cations including, but not limited to, alkali metals, such as potassium, lithium, or combinations thereof. The caustic solution may be a sodium hydroxide (NaOH) solution or a potassium hydroxide (KOH) solution having a concentration of 30 to 60% by weight, particularly 30 to 40% by weight. It will be appreciated that the caustic solution may be a solution of sodium hydroxide and potassium hydroxide having a total caustic concentration of 30 to 60 wt%, particularly 30 to 40 wt%.

The slurry can be heated for a sufficient time to convert the uncalcined lithium-containing silicate to the lithium-rich sodalite phase. The time required for extraction depends on the mineralogy and particle size of the uncalcined lithium-containing silicate, the concentration of the caustic solution, the solid density of the slurry, and the temperature conditions.

Those skilled in the art will appreciate that the higher the temperature, the shorter the reaction time to reach the desired level of extraction, all other things being equal.

Typically, the slurry is heated in an autoclave to 200 ℃ to 350 ℃, particularly 250 ℃ to 290 ℃. The time of the heating step may be 1 to 6 hours, particularly 2 hours.

The slurry may be agitated or mechanically agitated with an impeller or another agitator during the heating step, as is well known to those skilled in the art.

The heated slurry may then be diluted (110) with water to 10-30% w/w relative to the caustic solution.

The diluted slurry may then be subjected to conventional separation techniques to separate the lithium-rich sodalite phase from the diluted slurry. Suitable conventional separation techniques include, but are not limited to, filtration, gravity separation, centrifugation, and the like. One skilled in the art will appreciate that additives such as clarifiers and/or thickeners may be mixed into the diluted slurry prior to separating the solids from the liquid to facilitate efficient separation thereof. It is to be understood that the lithium-rich sodalite phase may be washed one or more times during the separation process.

The liquid remaining after separation of the lithium-rich sodalite phase (i.e., Primary Filtrate (PF)) may be combined with one or more of the caustic wash liquids previously described. The combined liquid contains soluble aluminum and silicon. When the combined liquids are treated with lime, soluble aluminum and silicon can be removed from the solution as calcium silicate and calcium aluminate and thereby regenerate the caustic solution. The combined liquids may be treated with a stoichiometric lime slurry (120) at a temperature of 60 ℃ to 80 ℃ to produce calcium silicate and aluminum silicate solids.

The solids may be isolated by conventional separation techniques. Suitable conventional separation techniques include, but are not limited to, filtration, gravity separation, centrifugation, and the like. One skilled in the art will appreciate that additives such as clarifiers and/or thickeners may be mixed into the diluted slurry prior to separation of solids from the liquor to facilitate efficient separation thereof. It is understood that the calcium aluminate and calcium silicate may undergo one or more washes during the separation process.

The inventors have found that in the heating step (100) of the process described herein, 70% to 95% of the Li is transferred to the lithium-rich sodalite phase, effectively separating the Li from the caustic solution, K, Si, and other impurities soluble in the slurry. In addition, the subsequent removal of silicate from the lithium-rich sodalite phase in one or more washing processes also provides good separation of Li from any Si dissolved in the heating step.

About 5% to 30% of the Li remains in the separated liquid optionally combined with one or more of the caustic washes previously described. As mentioned above, the combined liquor may be treated with lime to precipitate calcium aluminate and calcium silicate. The treated combined liquor may have a caustic strength of from 5 to 30% w/w. Advantageously, the separated treated combined liquor may be concentrated (130) to increase the caustic concentration of the combined liquor and recycled for use as the caustic solution in the heating step (100) of the process. In this way, lithium loss in the process is minimized and caustic solution is saved in the process. In some embodiments, the caustic concentration of the combined liquids may be increased to 30 to 60 wt% NaOH or KOH, particularly 30 to 40 wt% NaOH or KOH. The Li content of the concentrated combined liquid may be 1-4g/L Li.

The caustic strength of the combined liquids may be increased by evaporating the combined liquids for a period of time sufficient to increase the caustic strength to 30-60 wt%. In some embodiments, the combined liquids may be evaporated at a temperature of 80 ℃ to 150 ℃ at atmospheric pressure.

One skilled in the art will recognize that in some embodiments, the primary filtrate may be treated separately as described above to remove soluble aluminum and silicon in the form of calcium silicate and calcium aluminate. The caustic concentration of the treated primary filtrate may then be increased as described above, and the concentrated primary filtrate, or a portion thereof, may be recycled for use as the caustic solution in the heating step (100) of the process.

Alternatively, the caustic wash liquor may be treated one or more times as described above to remove soluble aluminum and silicon in the form of calcium silicate and calcium aluminate. The treated caustic wash liquor may then be increased in caustic concentration as described above and then recycled for use as the caustic solution in the heating step (100) of the process.

The treated primary filtrate, or a portion thereof, may optionally be combined with treated caustic wash liquor before being recycled for use as caustic solution in the heating step (100) of the process.

Extraction of Li from the lithium-rich sodalite phase may be achieved by leaching the lithium-rich sodalite phase (140) under relatively mild acidic conditions to produce a lithium-rich mother liquor containing high Li (up to 30g/L) and relatively low levels of major impurities (e.g., Al, Fe, and Si). The inventors believe that the mechanism of lithium extraction from the lithium-rich sodalite phase appears to be via an ion exchange mechanism (Li/H)⁺)。

In various embodiments, the lithium-rich sodalite phase is leached (140) with dilute acid at a temperature of 20 ℃ to 80 ℃. The time of the leaching step may be 1 to 24 hours, in particular 2 to 8 hours.

In one embodiment, the dilute acidic solution comprises a strong acid, such as HCl, HNO₃、H₂ SO₄Or a combination thereof. The pH of the dilute acid solution may be in the range of from 2 to 6, in particular from 3 to 5.

In various embodiments, the extraction of lithium from the lithium-rich sodalite phase into the lithium-rich mother liquor may be > 90%, particularly > 95%. In some embodiments, the lithium-rich mother liquor comprises 5 to 10g/L Li. Optionally, at least a portion of the lithium-rich mother liquor may be recycled for slurrying the lithium-rich sodalite phase, thereby increasing the lithium content of the resulting lithium-rich mother liquor.

The processes described herein can be performed in batch mode or continuous mode. The particular choice of operation will depend on the residence time required to extract the desired amount of lithium.

Method for recovering lithium salts from lithium-containing silicates

As previously described, after the lithium values are extracted from the lithium-containing material, the lithium values may then be recovered from the lithium-enriched solution as lithium salts, including but not limited to lithium carbonate, lithium hydroxide, lithium phosphate, or lithium sulfate.

One skilled in the art will recognize that one or more impurities may be co-dissolved with lithium in the lithium-rich mother liquor. As used herein, the term "impurity" refers to a metal value other than lithium contained in the lithium-rich sodalite phase, which is capable of dissolving under weakly acidic conditions. Examples of typical metal values other than lithium include, but are not limited to, K, Na, Cs, Rb, Si, Al, and Fe.

The lithium-rich mother liquor can be readily purified by adding (150) a suitable base such as a caustic (i.e., sodium hydroxide and/or sodium carbonate), a solution of potassium hydroxide or lithium hydroxide with chlorides or a solution of lime, caustic, potassium hydroxide or lithium hydroxide with sulfates prior to recovery of the desired lithium salt. As will be readily understood by those skilled in the art, the resulting impurity precipitate may be removed by conventional separation techniques. Calcium is often present in lithium-containing solutions, particularly in mother liquor, in undesirable concentrations because, as noted above, the mother liquor may have been previously treated with excess lime to precipitate metal impurities, such as calcium aluminate and calcium silicate, from the solution. It is common practice to reduce the calcium content by precipitating calcium carbonate by adding sodium carbonate to deplete (or "soften") the calcium mother liquor.

Some embodiments described in the present invention provide an alternative method for softening a lithium-rich mother liquor to reduce its calcium content from about 500ppm to less than 25ppm, particularly less than 20 ppm.

After removing impurities (150) from the lithium-rich mother liquor, the calcium content of the lithium-rich mother liquor may be reduced (160) by adding sodium carbonate to the lithium-rich mother liquor to produce a calcium precipitate such as calcium carbonate and magnesium carbonate. Sodium carbonate may be added to the lithium rich mother liquor as a 20% w/w solution at a temperature of from room temperature to 90 c, in particular from 50 c to 60 c. The amount of sodium carbonate added to the lithium-rich mother liquor may be sufficient to eliminate residual calcium content in the lithium-rich mother liquor or at least reduce the calcium content in the lithium-rich mother liquor to less than 25ppm, particularly 20 ppm.

Alternatively, the inventors have found that sodium phosphate can be added to the lithium rich mother liquor to facilitate the softening step (160) and to reduce the calcium content by producing calcium phosphate.

The sodium phosphate can be more than or equal to 100g/L Na₃PO₄The solution is added to the lithium-rich mother liquor in one or more equal portions, which may be added in stoichiometric proportions of more than 100% (wrt apatite formation), in particular in stoichiometric proportions of 200% to 500% (wrt apatite formation). In addition, any fluoride in the lithium-rich mother liquor may be phosphorus fluorideThe apatite form precipitates, thereby reducing the fluoride concentration to less than 5 ppm. The inventors believe that the main phases produced during the initial addition of potassium phosphate are calcium phosphate and hydroxyapatite.

It will be appreciated that in embodiments where the lithium-rich mother liquor has a high K content, the softening step may be achieved by adding potassium phosphate instead of sodium phosphate to the lithium-rich mother liquor in similar amounts as described above to produce calcium phosphate and fluorapatite (if fluoride is present in the lithium-rich mother liquor). Alternatively, another alkali metal phosphate may be used in the softening step.

Referring to the figure, the disclosed process also includes adding a phosphorus-containing compound to the softened lithium-rich mother liquor to precipitate lithium phosphate (170).

The phosphorus-containing compound may be added in the form of an aqueous solution. The phosphorus-containing compound may be selected from the group comprising phosphoric acid, potassium phosphate, sodium phosphate, or a combination thereof. It will be appreciated that the concentration of the aqueous solution of the phosphorus-containing compound is in fact limited by its solubility. For example, the concentration of the aqueous potassium phosphate solution may be 100g/L to 800 g/L. The phosphorus-containing compound may be added to the softened lithium-rich mother liquor in stoichiometric excess to ensure that less than 100mg/L of soluble lithium remains in solution and that more than 500mg/L, especially 500 to 3000mg/L, of P remains in solution.

In embodiments where the phosphorus-containing compound solution comprises phosphoric acid, hydroxide ions (e.g., KOH) may be added simultaneously to the softened lithium-rich mother liquor in an amount sufficient to maintain the pH of the solution above a threshold pH at which lithium phosphate may redissolve and increase soluble lithium in the solution to greater than 100 mg/L.

The phosphorus-containing compound may be added to the softened lithium-rich mother liquor to precipitate lithium phosphate at a temperature of from 50 ℃ to below the boiling point of the solution, in particular at a temperature of greater than 90 ℃.

The lithium phosphate precipitate may be separated from the solution by conventional separation techniques and washed in several steps. Suitable separation techniques include, but are not limited to, filtration, gravity separation, centrifugation, decantation, and the like. The mother liquor and wash filtrate may be combined and may be subjected to a dephosphorylation process (180) as described below.

The dephosphorylation process (180) includes adding calcium hydroxide to the filtrate or supernatant to produce tricalcium phosphate and/or apatite precipitates. The calcium hydroxide may be selected from the group consisting of hydrated lime (hydrated lime), quick lime (lime), hydrated lime (slaked lime), and mixtures thereof.

Tricalcium phosphate and/or apatite precipitates may be separated from the resulting liquid by conventional separation techniques. Suitable separation techniques include, but are not limited to, filtration, gravity separation, centrifugation, decantation, and the like. After removal of the excess phosphorus-containing compound, the lithium-depleted solution may be recycled to step a) or step b) to minimize lithium loss and/or optimize water balance.

In an alternative embodiment, lithium carbonate may be recovered from the lithium-rich mother liquor by increasing the carbonate content in the lithium-rich mother liquor to a concentration that exceeds the solubility limit of lithium carbonate. This can be readily accomplished by adding carbonate to the lithium-rich mother liquor to produce lithium carbonate solids and a lithium-depleted solution. Suitable carbonates include, but are not limited to, ammonium carbonate, sodium carbonate, potassium carbonate, or mixtures thereof.

Alternatively, lithium carbonate may be recovered from the lithium-rich mother liquor by contacting the lithium-rich mother liquor with carbon dioxide to produce lithium carbonate solids and a lithium-depleted solution. In some embodiments, carbon dioxide is sparged into the lithium-rich mother liquor at a steady rate. The temperature of the lithium-rich mother liquor may be in the range of 90 ℃ to 100 ℃.

The lithium carbonate solids produced may be separated from the lithium-depleted solution produced by conventional separation techniques described in the preceding paragraphs. The lithium-depleted solution may be recycled back to step b) of the process to minimize lithium loss.

In other alternative embodiments, lithium sulfate may be recovered from the lithium-rich mother liquor by increasing the sulfate content in the lithium-rich mother liquor to a concentration that exceeds the soluble lithium of the lithium sulfate. The increase in sulfate content can be achieved by evaporating the lithium rich mother liquor. The evaporation of the lithium-rich mother liquor can be carried out at atmospheric pressure or under reduced pressure. The temperature of evaporation of the lithium-rich mother liquor may be 80 ℃ to 150 ℃.

The lithium sulfate solids produced may be separated from the lithium-depleted solution produced by conventional separation techniques described in the preceding paragraphs. The lithium-depleted solution may be recycled back to step b) of the process to minimize lithium loss.

Alternatively, lithium hydroxide may be recovered from the lithium-rich mother liquor by adding sodium hydroxide to the lithium-rich mother liquor to increase the pH to greater than 10. The lithium-rich mother liquor may then be cooled to <10 ℃ to crystallize the niter salt therefrom. The nitrariat salt may be separated from the resulting lithium-rich mother liquor by conventional separation techniques, such as filtration.

The primary filtrate may be concentrated by evaporation to 50-90% of its volume and the lithium hydroxide solid crystallized from it. The evaporation can be carried out at atmospheric or reduced pressure and at a temperature of 80 ℃ to 150 ℃.

The lithium hydroxide solids can be separated from the concentrated primary filtrate to leave a lithium-depleted solution. In one embodiment, the lithium-depleted solution may be recycled back to step a) and/or step b) of the process to minimize lithium loss.

In the claims which follow and in the preceding description of the invention, unless the context requires otherwise due to express language or necessary implication, the word "comprise" or variations such as "comprises" or "comprising" is used in its inclusive sense, i.e. to specify the presence of the stated features in various embodiments of the invention, but not to preclude the presence or addition of further features.

It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the above-described embodiments without departing from the broad general scope of the disclosure. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.