MAGNETIC TITANIUM-BASED LITHIUM ADSORBENT AND PREPARATION METHOD THEREOF

Abstract

In order to resolve the problem that a magnetic lithium adsorbent in the related art is difficult to be used for lithium extraction from strong-alkaline and carbonate-type brines, a magnetic titanium-based lithium adsorbent is provided, which includes a magnetic composite and a lithium adsorption layer. The lithium adsorption layer is disposed at an outer surface of the magnetic composite. The magnetic composite includes a magnetic material and a titanium oxide. The lithium adsorption layer includes a lithium titanium oxide.

Claims

1. A magnetic titanium-based lithium adsorbent, comprising a magnetic composite and a lithium adsorption layer, wherein the lithium adsorption layer is disposed on an outer surface of the magnetic composite, the magnetic composite comprises a magnetic material and a titanium oxide, and the lithium adsorption layer comprises a lithium titanium oxide.

2. The magnetic titanium-based lithium adsorbent according to claim 1, wherein the magnetic composite comprises a magnetic core formed by the magnetic material and a titanium oxide coating layer formed by the titanium oxide, the magnetic core comprises one or more of Fe.sub.3O.sub.4, iron, cobalt, nickel, and ferrite, and the titanium oxide coating layer is coated on an outer surface of the magnetic core.

3. The magnetic titanium-based lithium adsorbent according to claim 2, wherein the titanium oxide coating layer comprises TiO.sub.2.

4. The magnetic titanium-based lithium adsorbent according to claim 3, wherein the magnetic core comprises Fe.sub.3O.sub.4.

5. The magnetic titanium-based lithium adsorbent according to claim 4, wherein a mole ratio of Ti in TiO.sub.2 to Fe in Fe.sub.3O.sub.4 is 1:2 to 1:5.

6. The magnetic titanium-based lithium adsorbent according to claim 2, wherein an average particle size of the magnetic composite is 20-120 nm.

7. The magnetic titanium-based lithium adsorbent according to claim 2, wherein an average particle size of the magnetic core is 10-100 nm, and a thickness of the titanium oxide coating layer is 5-20 nm.

8. The magnetic titanium-based lithium adsorbent according to claim 2, wherein a thickness of the lithium adsorption layer is 5-50 nm.

9. The magnetic titanium-based lithium adsorbent according to claim 1, wherein a saturation magnetization of the magnetic composite is 20-60 emu/g.

10. The magnetic titanium-based lithium adsorbent according to claim 1, wherein the lithium adsorption layer is a porous structure with a pore volume of 0.01 mL/g-0.30 mL/g.

11. The magnetic titanium-based lithium adsorbent according to claim 1, wherein the lithium titanium oxide is Li.sub.4-xTi.sub.5-yM.sub.yO.sub.12, and wherein x is selected from 0-2, y is selected from 0-0.1, and M is one or more of Mg, Cr, Co, Ni, Mo, Zr, and Zn.

12. The magnetic titanium-based lithium adsorbent according to claim 1, further comprising an outer coating layer, wherein the outer coating layer is disposed at an outer surface of the lithium adsorption layer, the outer coating layer comprises a metal oxide, the metal oxide is an oxide of one or more of Mg, Cr, Co, Ni, Mo, Zr, Ti, Zn, and Li, and a thickness of the outer coating layer is 1-10 nm.

13. A method for preparing a magnetic titanium-based lithium adsorbent, comprising: obtaining a magnetic composite comprising a magnetic material and a titanium oxide; preparing a precursor of the magnetic titanium-based lithium adsorbent by: mixing the magnetic composite, a titanium salt solution, and a lithium salt solution for reaction, and separating solid and liquid to obtain intermediate product particles; and calcining the intermediate product particles to form a lithium adsorption layer at an outer surface of the magnetic composite, and obtaining the precursor of the magnetic titanium-based lithium adsorbent; and adding the precursor of the magnetic titanium-based lithium adsorbent into an acidic solution to desorb a part of lithium from the lithium adsorption layer, and obtaining the magnetic titanium-based lithium adsorbent.

14. The method according to claim 13, wherein the obtaining the magnetic composite comprises: preparing an iron salt solution comprising ferrous ions and ferric ions; preparing a Fe.sub.3O.sub.4 dispersion by: adding aqueous ammonia into the iron salt solution dropwise at 40-60° C., and separating solid and liquid to obtain the Fe.sub.3O.sub.4 dispersion; and preparing a TiO.sub.2 dispersion from a nano-TiO.sub.2, mixing the TiO.sub.2 dispersion with the Fe.sub.3O.sub.4 dispersion, and separating solid and liquid to obtain the magnetic composite.

15. The method according to claim 14, wherein in the iron salt solution, a concentration of iron ions is 0.5-3 mol/L, and a mole ratio of the ferrous ions to the ferric ions is 1:2; and based on a weight of a solution of the TiO.sub.2 dispersion as 100%, TiO.sub.2 in the TiO.sub.2 dispersion is 10 wt. %-20 wt. %.

16. The method according to claim 14, wherein the obtained magnetic composite is washed with deionized water and absolute ethanol, dried, and ground to a particle size of 20-120 nm.

17. The method according to claim 13, wherein the preparing a precursor of the magnetic titanium-based lithium adsorbent comprises, after adding the magnetic composite into the titanium salt solution with stirring, adding the lithium salt solution into the titanium salt solution for reaction, and wherein a mole ratio of Fe in the magnetic composite to Li in the lithium salt solution is configured to be 1:5 to 1:10, and a mole ratio of Li in the lithium salt solution to Ti in the titanium salt solution is configured to be 0.5:1 to 1:3.

18. The method adsorbent according to claim 13, wherein the titanium salt solution comprises a solution of one or more of titanyl sulfate and metatitanic acid, and a concentration of the titanium salt solution is 1-4 mol/L; and the lithium salt solution comprises a solution of one or more of lithium chloride, lithium sulfate, lithium hydroxide, lithium nitrate, and lithium acetate, and a concentration of the lithium salt solution is 1-3 mol/L.

19. The method according to claim 13, wherein before the calcining the intermediate product particles, a metal salt is added into the intermediate product particles for doping.

20. The method according to claim 13, wherein after the calcining the intermediate product particles, a metal oxide is added into the precursor of the magnetic titanium-based lithium adsorbent for calcining.

Description

DETAILED DESCRIPTION

[0032] In order to make the technical problem to be resolved, technical solutions, and beneficial effects in the present disclosure more comprehensible, the present disclosure will be further described in detail with reference to the embodiments below. It should be understood that the embodiments described herein are merely used to explain the present disclosure but are not to limit the present disclosure.

[0033] An embodiment of the present disclosure provides a magnetic titanium-based lithium adsorbent including a magnetic composite and a lithium adsorption layer. The lithium adsorption layer is provided on an outer surface of the magnetic composite. The magnetic composite includes a magnetic material and a titanium oxide. The lithium adsorption layer includes a lithium titanium oxide.

[0034] The magnetic titanium-based lithium adsorbent includes a magnetic composite and a lithium adsorption layer. The lithium titanium oxide in the lithium adsorption layer acts as the lithium adsorbent, which has the feature of being able to adsorb lithium from strong-alkaline and carbonate-type brines, not reacting with carbonate in brines, and having a high stability in a strong alkaline environment, thereby the scope of application in lithium extraction from brines is effectively expanded. The magnetic composite includes a titanium oxide and a magnetic material. The magnetic material is used to provide the magnetic properties of the magnetic composite, so that the magnetic titanium-based lithium adsorbent for lithium adsorption can be magnetically recovered when an operation of lithium enrichment from brines is carried out by using the magnetic titanium-based lithium adsorbent. The titanium oxide can participate in the synthesis of lithium titanium oxide in the lithium adsorption layer, so that the binding of the magnetic composite and the lithium adsorption layer is tighter, effectively preventing the lithium adsorption layer from falling off the surface of the magnetic composite during the long-term use of the magnetic titanium-based lithium adsorbent, and prolonging the service life of the magnetic titanium-based lithium adsorbent.

[0035] In different embodiments, the lithium adsorption layer is provided on the entire outer surface or part of the outer surface of the magnetic composite.

[0036] In different embodiments, the magnetic material and the titanium oxide in the magnetic composite may be bound in different forms. For example, the magnetic material and the titanium oxide may be doped and mixed with each other, or the titanium oxide is used as a coating layer of the magnetic material.

[0037] In an embodiment, the magnetic composite includes a magnetic core and a titanium oxide coating layer, the magnetic core includes one or more of Fe.sub.3O.sub.4, iron, cobalt, nickel, and ferrite, and the titanium oxide coating layer coats an outer surface of the magnetic core.

[0038] The titanium oxide is used as the coating layer of the magnetic core. On the one hand, the titanium oxide has good chemical inertness, which can effectively protect and isolate the magnetic core therein, ensuring the stability of the magnetic core and avoiding failure of magnetism. On the other hand, the contact area between the magnetic composite and the lithium adsorption layer is also increased. Because the titanium oxide coating layer has good affinity with the lithium titanium oxide of the lithium adsorption layer, it is beneficial to increasing the bonding strength of the magnetic composite and the lithium adsorption layer.

[0039] In an embodiment, the magnetic material is Fe.sub.3O.sub.4, the titanium oxide coating layer is TiO.sub.2, and a mole ratio of Ti in TiO.sub.2 to Fe in Fe.sub.3O.sub.4 is 1:2 to 1:5.

[0040] Fe.sub.3O.sub.4 has strong magnetic properties and good stability, and has low material cost, which can show high magnetic properties, so it is beneficial to the magnetic separation operation on the magnetic titanium-based lithium adsorbent.

[0041] In other embodiments, the titanium oxide coating layer may be Ti.sub.3O.sub.5.

[0042] The above element proportions can ensure that the magnetic composite has enough Fe.sub.3O.sub.4 to satisfy its magnetization requirements, and enable TiO.sub.2 to effectively coat the surface of Fe.sub.3O.sub.4 and provide formation sites for the lithium titanium oxide of the lithium adsorption layer in the subsequent process.

[0043] In some embodiments, an average particle size of the magnetic composite is 20-120 nm, an average particle size of the magnetic core is 10-100 nm, a thickness of the titanium oxide coating layer is 5-20 nm, and a thickness of the lithium adsorption layer is 5-50 nm.

[0044] When the thickness of the titanium oxide coating layer is within the above range, the bonding strength of the lithium adsorption layer on the magnetic core can be significantly increased, preventing the lithium adsorption layer from falling off during repeated use, and the magnetic properties of the magnetic core are not significantly affected and satisfy the magnetization required for magnetic separation.

[0045] The lithium adsorption capacity of the magnetic titanium-based lithium adsorbent is determined by the content of the lithium adsorption layer, so when the thickness of the lithium adsorption layer is within the above range, the magnetic titanium-based lithium adsorbent has a high lithium adsorption capacity per unit volume.

[0046] In some embodiments, a saturation magnetization of the magnetic composite is 20-60 emu/g.

[0047] In some embodiments, the lithium adsorption layer has a porous structure with a pore volume of 0.01-0.30 mL/g. The pore volume of the lithium adsorption layer is measured by the BET specific surface area method.

[0048] When the lithium adsorption layer has a porous structure, the contact area between the lithium adsorption layer and the brine can be increased, thus facilitating the adsorption of lithium ions in the brine onto the lithium adsorption layer, increasing the lithium adsorption capacity of the magnetic titanium-based lithium adsorbent.

[0049] In some embodiments, the lithium titanium oxide is selected from Li.sub.4-xTi.sub.5-yM.sub.yO.sub.12, x being selected from 0-2, y being selected from 0-0.1, and M being one or more of Mg, Cr, Co, Ni, Mo, Zr, and Zn.

[0050] When x is 0, the lithium titanium oxide is in a full lithiation state, and it is necessary to carry out pre-desorption by an acidic solution to form vacancies by partial delithiation from the lithium titanium oxide, resulting in x of greater than 0. In this case, upon running into lithium ions in the brine, the lithium titanium oxide can allow the lithium ions to intercalate therein to reach a full lithiation state, and the lithium titanium oxide in the full lithiation state can be re-delithiated to enrich lithium ions, leading to reutilization of the magnetic titanium-based lithium adsorbent.

[0051] The metal element M can be intercalated into the lattice of the lithium titanium oxide by doping to improve the structural stability of the lithium titanium oxide and reduce the dissolution loss of titanium ions from the lithium titanium oxide during long-term soaking in the brine. When y is selected as 0, the lithium titanium oxide is not doped with the metal element M.

[0052] In some other embodiments, the magnetic titanium-based lithium adsorbent further includes an outer coating layer provided at an outer surface of the lithium adsorption layer, the outer coating layer is a metal oxide, the metal oxide is an oxide of one or more of Mg, Cr, Co, Ni, Mo, Zr, Ti, Zn, and Li, and a thickness of the outer coating layer is 1-10 nm.

[0053] By using the metal oxide as the outer coating layer coated outside the lithium adsorption layer, the lithium adsorption layer can be protected from being in direct contact with the brine, the molecular structure stability of the lithium adsorption layer is effectively ensured.

[0054] When the thickness of the outer coating layer is within the above range, the lithium adsorption layer can be effectively protected and the dissolution of titanium ions can be reduced. The outer coating layer of this thickness allows lithium ions to pass through and avoids blocking lithium ions, resulting in a high lithium-ion adsorption efficiency.

[0055] Another embodiment of the present disclosure provides a preparation method of the magnetic titanium-based lithium adsorbent above, including the following steps:

[0056] obtaining a magnetic composite: the magnetic composite includes a magnetic material and a titanium oxide;

[0057] preparing a precursor of the magnetic titanium-based lithium adsorbent: the magnetic composite, a titanium salt solution and a lithium salt solution are mixed for reaction, and intermediate product particles are obtained through separation of solid and liquid; and the intermediate product particles are calcined to form a lithium adsorption layer at an outer surface of the magnetic composite, to obtain the precursor of the magnetic titanium-based lithium adsorbent; and

[0058] pre-desorption: the precursor of the magnetic titanium-based lithium adsorbent is added into an acidic solution for pre-desorption to desorb a part of lithium from the lithium adsorption layer, to obtain the magnetic titanium-based lithium adsorbent.

[0059] The magnetic titanium-based lithium adsorbent prepared by the above preparation method can adsorb lithium ions from strong-alkaline and carbonate-type brines, and has a good structural stability and a long service life.

[0060] In some embodiments, a preparation method of the magnetic composite includes the following steps:

[0061] preparing an iron salt solution: the iron salt solution includes ferrous ions and ferric ions;

[0062] preparing a Fe.sub.3O.sub.4 dispersion: aqueous ammonia is added into the iron salt solution dropwise at 40-60° C., and the Fe.sub.3O.sub.4 dispersion is obtained through separation of solid and liquid; and

[0063] coating: a TiO.sub.2 dispersion is prepared from a nano-TiO.sub.2, the TiO.sub.2 dispersion is mixed with the Fe.sub.3O.sub.4 dispersion, and the magnetic composite is obtained through separation of solid and liquid.

[0064] Fe.sub.3O.sub.4 in the Fe.sub.3O.sub.4 dispersion prepared by the above method has a large particle size to form a Fe.sub.3O.sub.4 core. TiO.sub.2 in the solution of the TiO.sub.2 dispersion has a small particle size. When the Fe.sub.3O.sub.4 dispersion and the TiO.sub.2 dispersion are mixed, TiO.sub.2 self-assembles on the surface of the Fe.sub.3O.sub.4 core to form the TiO.sub.2 coating layer to further form the magnetic composite. The above method has the advantages of a low synthesis temperature, a short reaction time, and a uniform particle size of the prepared magnetic composite.

[0065] In an embodiment, the Fe.sub.3O.sub.4 dispersion may be added into the TiO.sub.2 dispersion dropwise, or the TiO.sub.2 dispersion may be added into the Fe.sub.3O.sub.4 dispersion dropwise.

[0066] In some embodiments, both the Fe.sub.3O.sub.4 dispersion and the TiO.sub.2 dispersion are in the form of colloids.

[0067] In some embodiments, preparing a Fe.sub.3O.sub.4 dispersion includes heating in a water bath to keep the temperature of the iron salt solution at 40-60° C., dropwise adding the aqueous ammonia includes rapid adding and then slow adding the aqueous ammonia with stirring at 200-500 rpm to adjust the pH value of the solution to 11, aging for 2-8 h after reaction for 1-4 h, and repeatedly washing, centrifuging, separating, and dispersing of the resulting product, to obtain the Fe.sub.3O.sub.4 dispersion.

[0068] In some embodiments, in the iron salt solution, a concentration of iron ions is 0.5-3 mol/L, and a mole ratio of ferrous ions to ferric ions is 1:2, and based on a weight of the solution of the TiO.sub.2 dispersion as 100%, TiO.sub.2 in the TiO.sub.2 dispersion is 10 wt. %-20 wt. %.

[0069] In an embodiment, the ferrous ions are derived from ferrous chloride (FeCl.sub.2.Math.4H.sub.2O), the ferric ions are derived from ferric chloride (FeCl.sub.3.Math.6H.sub.2O), the solvent of the iron salt solution is deionized water, and ferrous chloride and ferric chloride are added together into deionized water with stirring to fully dissolve therein.

[0070] In other embodiments, the ferrous ions and the ferric ions may be derived from other iron salts such as FeSO.sub.4 and Fe.sub.2(SO.sub.4).sub.3.

[0071] The intermediate product Fe.sub.3O.sub.4 contains both iron(II) and iron(III) in a ratio of 1:2, so the mole ratio of the ferrous ions to the ferric ions is configured to be 1:2 to effectively ensure the purity of Fe.sub.3O.sub.4 and prevent the resulted Fe.sub.3O.sub.4 from containing non-magnetic substances such as FeO and Fe.sub.2O.sub.3.

[0072] In some embodiments, in the step of coating, the solution of the TiO.sub.2 dispersion is heated in a water bath to 40-60° C., the Fe.sub.3O.sub.4 dispersion is added into the solution of the TiO.sub.2 dispersion dropwise, and then the resultant solution is stirred at 200-400 rpm for 1-4 h.

[0073] In some embodiments, the obtained magnetic composite is washed with deionized water and absolute ethanol, dried, and ground to a particle size of 20-120 nm.

[0074] In an embodiment, the solid-liquid separation is carried out by using a centrifuge at a rotational speed of 2500-4500 rpm for 10-60 min to obtain the magnetic composite. The separated magnetic composite is washed at a stirring speed of 150-500 rpm with deionized water and absolute ethanol at 10-30° C., and then filtered and separated to obtain a filtered substance. The filtered substance is washed with deionized water in a ratio of 1:(5-50) for 5-20 min each time, a total of 2-5 times. Through washing, ionic impurities can be effectively removed from the magnetic composite, thereby avoiding the influence of the ionic impurities on the subsequent preparation of the lithium adsorption layer.

[0075] The washed magnetic composite is placed in a vacuum drying oven to dry at 60-90° C. for 5-12 h. The dried magnetic composite is ground in an agate crucible for 1-3 h to obtain the magnetic composite with an average particle size of 30-80 nm and a saturation magnetization of 20-60 emu/g.

[0076] In some embodiments, in the step of preparing a precursor of the magnetic titanium-based lithium adsorbent, the magnetic composite is added into the titanium salt solution with stirring at a speed of 300-500 rpm, and then the lithium salt solution is added for reaction with a mole ratio of Fe in the magnetic composite to Li in the lithium salt solution being configured to be 1:5 to 1:10 and a mole ratio of Li in the lithium salt solution to Ti in the titanium salt solution being configured to be 0.5:1 to 1:3.

[0077] The titanium salt solution is selected from titanium salts that can react with lithium ions to precipitate.

[0078] In an embodiment, in the step of preparing a precursor of the magnetic titanium-based lithium adsorbent, the titanium salt solution includes a solution of one or more of titanyl sulfate and metatitanic acid, and a concentration of the titanium salt solution is 1-4 mol/L; and the lithium salt solution includes a solution of one or more of lithium chloride, lithium sulfate, lithium hydroxide, lithium nitrate, and lithium acetate, and a concentration of the lithium salt solution is 1-3 mol/L.

[0079] The titanium salt solution dissolves at 20-60° C. at a stirring speed of 150-500 rpm.

[0080] A stirring speed of the lithium salt solution is 150-500 rpm.

[0081] In an embodiment, the lithium salt solution is selected from a lithium hydroxide solution. Compared with other lithium salt solutions, when the lithium salt solution is selected from the lithium hydroxide solution, the lithium adsorption layer with a porous structure can be formed, thereby effectively increasing the lithium adsorption capacity from the brine.

[0082] In some embodiments, in the step of preparing a precursor of the magnetic titanium-based lithium adsorbent, the magnetic composite, the titanium salt solution, and the lithium salt solution are mixed and stirred for 1-4 h, and then left for aging at 10-30° C. for 5-20 h, to obtain a mixture, and the mixture is filtered by using a vacuum filter in a negative pressure of 0.02-0.08 MPa to obtain intermediate product particles. The intermediate product particles obtained after filtering are washed with deionized water at a stirring speed of 100-300 rpm at 10-30° C. to obtain a filtered substance, and the filtered substance is washed with deionized water in a ratio of 1:(5-50) for 5-20 min. The washing temperature and speed should not be too high, and the washing time should not be too long, so as to avoid the structure damage of the intermediate product particles. The intermediate product particles obtained after washing are filtered by using a vacuum filter in a negative pressure of 0.02-0.08 MPa.

[0083] The intermediate product particles are calcined in an air atmosphere at 350-550° C. for 4-12 h to form the lithium adsorption layer on the surface of the magnetic composite. In this embodiment, the obtained lithium adsorption layer in a full lithiation state is Li.sub.4Ti.sub.5O.sub.12.

[0084] In some embodiments, before the calcining, a metal salt is added into the intermediate product particles for doping, and the metal salt includes a salt of one or more of Mg, Cr, Co, Ni, Mo, Zr, and Zn.

[0085] During the calcining, metal ions of the metal salt will be doped into the lattice of the lithium adsorption layer to replace some of titanium, so that the obtained lithium adsorption layer has a more stable structure.

[0086] In some embodiments, after the calcining, a metal oxide is added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating, and the metal oxide includes an oxide of one or more of Mg, Cr, Co, Ni, Mo, Zr, Ti, Zn, and Li.

[0087] In some embodiments, the precursor of the magnetic titanium-based lithium adsorbent is partially delithiated through the pre-desorption, so that the lithium adsorption layer is in the delithiation state and provides vacancies for lithium, and thus has the capability of lithium adsorption. In an embodiment, the precursor of the magnetic titanium-based lithium adsorbent is pre-desorbed with an acidic solution in a solid-liquid mass ratio of 1:(10-100), stirring at 150-400 rpm, at 20-50° C. for 2-10 h. The acidic solution is selected from one or more of a sulfuric acid solution, a hydrochloric acid solution, and a nitric acid solution. An acid concentration of the acidic solution is 0.5-2 mol/L. In this embodiment, the obtained lithium adsorption layer after pre-desorption is Li.sub.4-xTi.sub.5O.sub.12.

[0088] The present disclosure is further described through the following examples.

Example 1

[0089] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including the following steps.

[0090] At room temperature, FeCl.sub.2 and FeCl.sub.3 were formulated in a mole ratio of 1:2 into an iron salt solution of a concentration of 0.5 mol/L, a nano-TiO.sub.2 was formulated into 10 wt % of TiO.sub.2 colloid solution, lithium hydroxide was formulated into a lithium salt solution of a concentration of 3 mol/L, and titanyl sulfate was formulated into a titanium salt solution of a concentration of 3 mol/L.

[0091] While stirring at 200 rpm, aqueous ammonia was added into the iron salt solution dropwise at 50° C. to adjust the pH value of the solution to 11. After reacting for 1 h and then aging for 4 h, the obtained product was washed, centrifuged, and separated to obtain a pure Fe.sub.3O.sub.4 colloid solution. The TiO.sub.2 colloid was added in the Fe.sub.3O.sub.4 colloid solution dropwise in a titanium-iron mole ratio of 1:3 and then stirred at 200 rpm for 2 h. Solid-liquid separation was carried out by using a centrifuge. The separated substance was washed and then dried in a vacuum drying oven. The dried substance was ground for 1 h to obtain a magnetic composite Fe.sub.3O.sub.4/TiO.sub.2. The magnetic composite was slowly added into the titanium salt solution while stirring, followed by adding the lithium salt solution, to make a mole ratio of iron to lithium 1:5 and a mole ratio of lithium to titanium 1:2. The resultant mixture was stirred for 4 h and then aged for 10 h, and then filtered by using a vacuum filter to obtain intermediate product particles. After washing and filtering, the intermediate product particles were placed in a muffle furnace and calcined in an air atmosphere at 500° C. for 12 h to obtain a precursor of a magnetic titanium-based lithium adsorbent with a lithium adsorption layer of full lithiation state Li.sub.4Ti.sub.5O.sub.12. The precursor of the magnetic titanium-based lithium adsorbent was added in 0.5 mol/L sulfuric acid to carry out pre-desorption in a solid-liquid mass ratio of 1:20 while stirring at 200 rpm for 4 h to obtain the magnetic titanium-based lithium adsorbent with the lithium adsorption layer of delithiation-state Li.sub.2.2Ti.sub.5O.sub.12. In this case, the particle size of the magnetic core Fe.sub.3O.sub.4 was 90 nm, the thickness of the TiO.sub.2 layer was 10 nm, and the thickness of the Li.sub.2.2Ti.sub.5O.sub.12 layer was 30 nm.

Example 2

[0092] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0093] The lithium salt solution was selected from a lithium chloride solution of a concentration of 2 mol/L.

[0094] The titanium salt solution was selected from a metatitanic acid solution of a concentration of 2 mol/L.

[0095] The calcining was carried out at 400° C. for 5 h.

Example 3

[0096] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0097] The concentration of the TiO.sub.2 colloid was 20 wt %.

[0098] The TiO.sub.2 colloid was added into the Fe.sub.3O.sub.4 colloid in a titanium-iron mole ratio of 1:2. The thickness of the TiO.sub.2 layer was 20 nm.

Example 4

[0099] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0100] The concentration of the TiO.sub.2 colloid was 5 wt %.

[0101] The TiO.sub.2 colloid was added into the Fe.sub.3O.sub.4 colloid in a titanium-iron mole ratio of 1:6. The thickness of the TiO.sub.2 layer was 2 nm.

Example 5

[0102] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0103] The concentration of the TiO.sub.2 colloid was 20 wt %.

[0104] The TiO.sub.2 colloid was added into the Fe.sub.3O.sub.4 colloid in a titanium-iron mole ratio of 1:1. The thickness of the TiO.sub.2 layer was 30 nm.

Example 6

[0105] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0106] Lithium hydroxide was formulated into a lithium salt solution of a concentration of 0.5 mol/L. Titanyl sulfate was formulated into a titanium salt solution of a concentration of 0.5 mol/L.

[0107] The thickness of the formed Li.sub.2.2Ti.sub.5O.sub.12 layer was 8 nm.

Example 7

[0108] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0109] Lithium hydroxide was formulated into a lithium salt solution of a concentration of 0.1 mol/L. Titanyl sulfate was formulated into a titanium salt solution of a concentration of 0.1 mol/L.

[0110] The thickness of the formed Li.sub.2.2Ti.sub.5O.sub.12 layer was 3 nm.

Example 8

[0111] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0112] Lithium hydroxide was formulated into a lithium salt solution of a concentration of 6 mol/L. Titanyl sulfate was formulated into a titanium salt solution of a concentration of 6 mol/L.

[0113] The thickness of the formed Li.sub.2.2Ti.sub.5O.sub.12 layer was 60 nm.

Example 9

[0114] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0115] Before the calcining, Mg(NO.sub.3).sub.2 was added into the intermediate product particles for doping. Then, the lithium adsorption layer of the obtained magnetic titanium-based lithium adsorbent was Li.sub.2.2Ti.sub.4.9Mg.sub.0.1O.sub.12.

Example 10

[0116] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0117] Before the calcination, CoCO.sub.3 was added into the intermediate product particles for doping. Then, the lithium adsorption layer of the obtained magnetic titanium-based lithium adsorbent was Li.sub.2.2Ti.sub.4.9Co.sub.0.1O.sub.12.

Example 11

[0118] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0119] Before the calcining, Zn(NO.sub.3).sub.2 was added into the intermediate product particles for doping. Then, the lithium adsorption layer of the obtained magnetic titanium-based lithium adsorbent was Li.sub.2.2Ti.sub.4.9Zn.sub.0.1O.sub.12.

Example 12

[0120] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0121] After the calcining, ZnO was added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating. The thickness of the outermost ZnO coating layer was 5 nm.

Example 13

[0122] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0123] After the calcining, ZnO was added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating. The thickness of the outermost ZnO coating layer was 0.3 nm.

Example 14

[0124] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences. After the calcining, ZnO was added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating. The thickness of the outermost ZnO coating layer was 15 nm.

Example 15

[0125] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0126] After the calcining, MgO was added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating. The thickness of the outermost MgO coating layer was 5 nm.

Example 16

[0127] This example is used to describe the magnetic titanium-based lithium adsorbent and the preparation method thereof disclosed in the present disclosure, including most of the steps in Example 1 with the following differences.

[0128] After the calcination, Li.sub.2O was added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating. The thickness of the outermost Li.sub.2O coating layer was 5 nm.

Comparative Example 1

[0129] This comparative example provides a magnetic manganese-based lithium adsorbent and a preparation method thereof, including the following steps:

[0130] Fe.sub.3O.sub.4 was added into a mixed solution of ethanol and water in a volume ratio of 1:1. Tetraethyl orthosilicate was added while stirring to a silicon-iron mole ratio of 1:3, stirred for 5 h, and then subjected to solid-liquid separation, to obtain a Fe.sub.3O.sub.4/SiO.sub.2 composite. The Fe.sub.3O.sub.4/SiO.sub.2 composite was added into a manganese chloride solution of a concentration of 2 mol/L while stirring at 500 rpm, followed by adding a lithium hydroxide solution of a concentration of 3 mol/L, to make a mole ratio of iron to manganese 1:2 and a mole ratio of lithium to manganese 5:1. The resultant mixture was stirred for 1 h and then left for aging for 12 h to obtain a magnetic lithium manganese compound. After separation and oven-drying, the magnetic lithium manganese compound was placed in a muffle furnace and calcined at 350° C. for 5 h to obtain a precursor of the magnetic manganese-based lithium adsorbent. The precursor was added into 0.5 mol/L sulfuric acid and stirred for 5 h to obtain a magnetic manganese dioxide lithium ion sieve.

Comparative Example 2

[0131] This comparative example provides a magnetic titanium-based lithium adsorbent and a preparation method thereof, including most of the steps in Example 1 and the difference including follows.

[0132] A preparation method of a magnetic composite is as follows. Fe.sub.3O.sub.4 was added into a mixed solution of ethanol and water in a volume ratio of 1:1. Tetraethyl orthosilicate was added while stirring to a silicon-iron mole ratio of 1:3, stirred for 5 h, and then subjected to solid-liquid separation, to obtain a Fe.sub.3O.sub.4/SiO.sub.2 composite.

[0133] By replacing the magnetic composite Fe.sub.3O.sub.4/TiO.sub.2 in Example 1, the Fe.sub.3O.sub.4/SiO.sub.2 composite was used for subsequent steps.

[0134] Performance Test

[0135] The above prepared magnetic titanium-based lithium adsorbents and magnetic manganese-based lithium adsorbent were subjected to the following performance tests.

[0136] Adsorption Performance Test:

[0137] A magnetic adsorbent was subjected to the adsorption performance test with a lithium-containing brine of pH 12. The lithium-containing brine contained 1 g/L Li.sup.+ and 30 g/L Nat 10 g of magnetic adsorbent was weighed to carry out adsorption in a solid-liquid mass ratio of 1:30 at room temperature for 120 min while stirring at 300 rpm. After the adsorption, the magnetic adsorbent was filtered. Desorption was carried out with 0.1 mol/L sulfuric acid in a solid-liquid mass ratio of 1:10 for 30 min while stirring at 300 rpm. The obtained Li.sup.+ concentration after adsorption, Li.sup.+ adsorption capacity, Li.sup.+ concentration in desorption solution, Ti/Mn dissolution loss, and saturation magnetization of adsorbent are shown in Table 1. The above steps were repeated for 50 times to obtain the Li.sup.+ adsorption capacity shown in Table 1.

TABLE-US-00001 TABLE 1 Li.sup.+ Li.sup.+ Li.sup.+ Ti/Mn Li.sup.+ concentration adsorption concentration in dissolution loss adsorption capacity Saturation Pore after adsorption capacity desorption solution after one time after 50 times magnetization volume Test (mg/L) (mg/g) (g/L) (%) (mg/g) (emu/g) (mL/g) Example 1 37 28.89 2.75 0.09 26.59 50.1 0.25 Example 2 291 21.27 1.94 0.17 19.46 48.7 0.10 Example 3 49 28.53 2.70 0.13 22.64 27.3 0.25 Example 4 39 28.83 2.69 0.14 22.39 52.9 0.25 Example 5 40 28.80 2.73 0.11 25.68 19.1 0.25 Example 6 137 25.89 2.24 0.14 24.19 50.5 0.25 Example 7 254 22.38 2.11 0.15 20.64 50.8 0.25 Example 8 32 29.04 2.79 0.10 28.12 47.9 0.25 Example 9 60 28.20 2.74 0.05 27.50 49.8 0.22 Example 10 114 26.58 2.55 0.08 24.94 49.6 0.18 Example 11 97 27.09 2.61 0.07 25.77 49.8 0.19 Example 12 82 27.54 2.62 0.03 27.13 49.5 0.20 Example 13 71 27.87 2.65 0.05 27.11 49.7 0.21 Example 14 122 26.34 2.51 0.04 25.87 48.9 0.17 Example 15 104 26.88 2.60 0.04 26.24 49.1 0.18 Example 16 116 26.52 2.55 0.05 25.97 49.3 0.19 Comparative 577 12.69 1.26 64.5 — 33.6 0.30 Example 1 Comparative 71 27.87 2.65 0.40 9.5 49.0 0.24 Example 2

[0138] It can be learned from the test results of Examples 1-16 and Comparative Example 1 in Table 1 that in the case of lithium adsorption from strong-alkaline brines, after lithium adsorption to and desorption from the magnetic titanium-based lithium adsorbent prepared by the preparation method provided in the present disclosure, it has the adsorption capacity significantly increased compared with the magnetic manganese-based lithium adsorbent in the related art, and the low Ti dissolution loss, while the magnetic manganese-based lithium adsorbent has the Mn dissolution loss of up to 64.5%, and allows the brine to be pink after adsorption due to dissolution of a mass of Mn.

[0139] It can be learned from the test results of Examples 1 and 2 that the choice between lithium salt and titanium salt also has a certain influence on the adsorption and desorption performance and porosity of the magnetic titanium-based lithium adsorbent. When the lithium salt is selected from lithium hydroxide and the titanium salt is selected from titanyl sulfate, it is beneficial to the formation of the porous structure of the lithium adsorption layer, thereby increasing the lithium adsorption capacity.

[0140] It can be learned from the test results of Examples 1 and 3-5 that the thickness of the TiO.sub.2 layer in the magnetic composite has a certain influence on the bonding strength of the lithium adsorption layer and the saturation magnetization of the magnetic composite. When the thickness of the TiO.sub.2 layer is 5-20 nm, the effective binding of the lithium adsorption layer and the magnetic composite can be further ensured while avoiding the influence on the saturation magnetization, which is beneficial to the magnetic separation and recovery operation.

[0141] It can be learned from the test results of Examples 1 and 6-8 that when the thickness of the Li.sub.4-xTi.sub.5O.sub.12 layer is within 5-50 nm, the magnetic titanium-based lithium adsorbent has a good lithium adsorption capacity and maintains a good saturation magnetization.

[0142] It can be learned from the test results of Examples 1 and 9-16 that by doping a metal salt or coating a metal oxide, the adsorption performance of the magnetic titanium-based lithium adsorbent can be maintained to a certain extent, and the dissolution loss of titanium can be reduced. It can be learned from the test results of Examples 12-14 that when the thickness of the outer coating layer is within 1-10 nm, a complete coating can be formed on the magnetic titanium-based lithium adsorbent, which is beneficial to the intercalation and deintercalation of lithium ions.

[0143] It can be learned from the test results of Example 1 and Comparative Example 2 that TiO.sub.2 in the magnetic composite can increase the bonding strength of the magnetic composite and the lithium adsorption layer, thereby helping maintain the stability of Li.sup.+ adsorption performance after multiple times of use.

[0144] The foregoing descriptions are merely some embodiments of the present disclosure, but are not to limit the present disclosure. Any modification, equivalent replacement, and improvement made within the spirit and principle of the present disclosure shall fall within the protection scope of the present disclosure.