Patent Application
20230191361
This application is based on and claims priority to and benefits of Chinese Patent Application No. 202111567446.9, filed on Dec. 20, 2021. The entire content of the above-referenced application is incorporated herein by reference.
The present disclosure relates to the technical field of magnetic lithium adsorbent materials, and specifically, to a magnetic titanium-based lithium adsorbent and a preparation method thereof.
With the rapid development of electric bicycles, electric vehicles, and electronics industries, lithium batteries and lithium power batteries have become indispensable products, and the global demand for lithium resources is consequently increased. Salt lake brine and seawater are rich in liquid lithium resources, which are main resources for the future lithium production industry. Therefore, how to extract lithium from these liquid minerals has become a significant issue. At present, lithium extraction by adsorption is regarded as the most promising method for lithium extraction. In recent years, lithium adsorbents, extensively studied by researchers as a novel material, have a memory effect for lithium ions to some extent, stable adsorption capacity and elution rate due to lithiation. In order to facilitate the recovery of lithium adsorbents, magnetic materials are usually introduced into the lithium adsorbents.
In the related art, provided is a magnetic aluminum-based lithium adsorbent produced by a process as follows: Fe3O4 powder is added into deionized water with a dispersing agent. With aid of ultrasonic and strong stirring, AlCl3 powder is added into the resultant Fe3O4 dispersion for full dissolution by dispersing and stirring. Next, sodium hydroxide powder is added into the resultant system to gradually precipitate aluminum hydroxide at the interface of Fe3O4, to obtain a magnetic core @Al(OH)3·nH2O. Then, LiCl powder is added into the above system to disperse and react, to obtain a magnetic core @LiX·2Al(OH)3·nH2O. The above mixed solution is subjected to solid-liquid separation by using a magnetic separator, a filter press, or a centrifuge to obtain a dehydrated magnetic core @LiX·2Al(OH)3·nH2O as a magnetic aluminum-based lithium adsorbent.
In the related art, a magnetic lithium manganese spinel is produced additionally by a process as follows: Fe3O4 powder is added into a mixed solution of ethanol and water. Tetraethyl orthosilicate is added with stirring for a certain time. The resultant mixed solution is pumped into an electromagnetic separator again to magnetically separate a silicon dioxide-coated magnetic core Fe3O4. With stirring, the silicon dioxide-coated magnetic core Fe3O4 is pumped into a manganese chloride solution with addition of a lithium hydroxide solution, and is left for aging to obtain a magnetic lithium manganese compound. The magnetic lithium manganese compound is oven-dried at 60° C. and then placed in a furnace at 350° C. to calcine for 5 h, to obtain a magnetic lithium manganese spinel.
The magnetic aluminum-based lithium adsorbent and magnetic lithium manganese spinel in the related art are not suitable for adsorbing lithium from strong-alkaline and carbonate-type brines. The magnetic aluminum-based lithium adsorbent, which will react with carbonate to form a precipitate, is only suitable for adsorbing lithium from chloride-type brines. The magnetic lithium manganese spinel is prone to dissolution loss of Mn in a weak acid and strong alkaline environment, resulting in a decrease in adsorption performance, which is only suitable for adsorbing lithium from neutral to weak alkaline brines. According to another aspect, the lithium adsorbent in the related art tends to separate from its magnetic core due to insufficient binding. After a number of runs, the lithium adsorbent is difficult to recover due to the separation of the outer adsorbent and the magnetic core.
In order to resolve the problem that an existing magnetic lithium adsorbent is difficult to be used for lithium extraction from strong-alkaline and carbonate-type brines, the present disclosure provides a magnetic titanium-based lithium adsorbent and a preparation method thereof.
The technical solutions adopted by the present disclosure to resolve the above technical problem are as follows.
According to an aspect, the present disclosure provides a magnetic titanium-based lithium adsorbent including a magnetic composite and a lithium adsorption layer. The lithium adsorption layer is disposed 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.
In an embodiment, the magnetic composite includes a magnetic core formed by the magnetic material and a titanium oxide coating layer formed by the titanium oxide, the magnetic core includes one or more of Fe3O4, iron, cobalt, nickel, and ferrite, and the titanium oxide coating layer is coated on an outer surface of the magnetic core.
In an embodiment, the magnetic core is Fe3O4, the titanium oxide coating layer includes TiO2, and a mole ratio of Ti in TiO2 to Fe in Fe3O4 is 1:2 to 1:5.
In an embodiment, 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.
In an embodiment, a saturation magnetization of the magnetic composite is 20-60 emu/g.
In an embodiment, the lithium adsorption layer is a porous structure with a pore volume of 0.01 mL/g-0.30 mL/g.
In an embodiment, the lithium titanium oxide is Li4-xTi5-yMyO12, 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.
In an embodiment, the magnetic titanium-based lithium adsorbent further includes an outer coating layer disposed at an outer surface of the lithium adsorption layer, the outer coating layer includes 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.
According to another aspect, the present disclosure provides a method for preparing a magnetic titanium-based lithium adsorbent, including the following steps.
obtaining a magnetic composite including a magnetic material and a titanium oxide;
preparing a precursor of the magnetic titanium-based lithium adsorbent by: 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
the precursor of the magnetic titanium-based lithium adsorbent is added into an acidic solution to desorb a part of lithium from the lithium adsorption layer, to obtain the magnetic titanium-based lithium adsorbent.
In an embodiment, a preparation method of the magnetic composite includes the following steps:
preparing an iron salt solution including ferrous ions and ferric ions;
preparing a Fe3O4 dispersion by: aqueous ammonia is added into the iron salt solution dropwise at 40-60° C., and the Fe3O4 dispersion is obtained through separation of solid and liquid; and
a TiO2 dispersion is prepared from a nano-TiO2, the TiO2 dispersion is mixed with the Fe3O4 dispersion, and the magnetic composite is obtained through separation of solid and liquid.
In an embodiment, 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 the solution of the TiO2 dispersion as 100%, TiO2 in the TiO2 dispersion is 10 wt. %-20 wt. %.
In an embodiment, the obtained magnetic composite is washed with deionized water and absolute ethanol, dried, and ground to a particle size of 20-120 nm.
In an embodiment, 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 with 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.
In an embodiment, 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.
In an embodiment, before the calcining the intermediate product particles, a metal salt is added into the intermediate product particles for doping.
In an embodiment, after the calcining the intermediate product particles, a metal oxide is added into the precursor of the magnetic titanium-based lithium adsorbent for calcining.
The magnetic titanium-based lithium adsorbent provided in the present disclosure 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 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.
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.
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.
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.
In different embodiments, the lithium adsorption layer is provided on the entire outer surface or part of the outer surface of the magnetic composite.
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.
In an embodiment, the magnetic composite includes a magnetic core and a titanium oxide coating layer, the magnetic core includes one or more of Fe3O4, iron, cobalt, nickel, and ferrite, and the titanium oxide coating layer coats an outer surface of the magnetic core.
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.
In an embodiment, the magnetic material is Fe3O4, the titanium oxide coating layer is TiO2, and a mole ratio of Ti in TiO2 to Fe in Fe3O4 is 1:2 to 1:5.
Fe3O4 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.
In other embodiments, the titanium oxide coating layer may be Ti3O5.
The above element proportions can ensure that the magnetic composite has enough Fe3O4 to satisfy its magnetization requirements, and enable TiO2 to effectively coat the surface of Fe3O4 and provide formation sites for the lithium titanium oxide of the lithium adsorption layer in the subsequent process.
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.
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.
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.
In some embodiments, a saturation magnetization of the magnetic composite is 20-60 emu/g.
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.
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.
In some embodiments, the lithium titanium oxide is selected from Li4-xTi5-yMyO12, 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.
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.
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.
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.
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.
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.
Another embodiment of the present disclosure provides a preparation method of the magnetic titanium-based lithium adsorbent above, including the following steps:
obtaining a magnetic composite: the magnetic composite includes a magnetic material and a titanium oxide;
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
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.
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.
In some embodiments, a preparation method of the magnetic composite includes the following steps:
preparing an iron salt solution: the iron salt solution includes ferrous ions and ferric ions;
preparing a Fe3O4 dispersion: aqueous ammonia is added into the iron salt solution dropwise at 40-60° C., and the Fe3O4 dispersion is obtained through separation of solid and liquid; and
coating: a TiO2 dispersion is prepared from a nano-TiO2, the TiO2 dispersion is mixed with the Fe3O4 dispersion, and the magnetic composite is obtained through separation of solid and liquid.
Fe3O4 in the Fe3O4 dispersion prepared by the above method has a large particle size to form a Fe3O4 core. TiO2 in the solution of the TiO2 dispersion has a small particle size. When the Fe3O4 dispersion and the TiO2 dispersion are mixed, TiO2 self-assembles on the surface of the Fe3O4 core to form the TiO2 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.
In an embodiment, the Fe3O4 dispersion may be added into the TiO2 dispersion dropwise, or the TiO2 dispersion may be added into the Fe3O4 dispersion dropwise.
In some embodiments, both the Fe3O4 dispersion and the TiO2 dispersion are in the form of colloids.
In some embodiments, preparing a Fe3O4 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 Fe3O4 dispersion.
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 TiO2 dispersion as 100%, TiO2 in the TiO2 dispersion is 10 wt. %-20 wt. %.
In an embodiment, the ferrous ions are derived from ferrous chloride (FeCl2·4H2O), the ferric ions are derived from ferric chloride (FeCl3·6H2O), 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.
In other embodiments, the ferrous ions and the ferric ions may be derived from other iron salts such as FeSO4 and Fe2(SO4)3.
The intermediate product Fe3O4 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 Fe3O4 and prevent the resulted Fe3O4 from containing non-magnetic substances such as FeO and Fe2O3.
In some embodiments, in the step of coating, the solution of the TiO2 dispersion is heated in a water bath to 40-60° C., the Fe3O4 dispersion is added into the solution of the TiO2 dispersion dropwise, and then the resultant solution is stirred at 200-400 rpm for 1-4 h.
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.
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.
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.
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.
The titanium salt solution is selected from titanium salts that can react with lithium ions to precipitate.
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.
The titanium salt solution dissolves at 20-60° C. at a stirring speed of 150-500 rpm.
A stirring speed of the lithium salt solution is 150-500 rpm.
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.
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.
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 Li4Ti5O12.
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.
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.
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.
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 Li4-xTi5O12.
The present disclosure is further described through the following examples.
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.
At room temperature, FeCl2 and FeCl3 were formulated in a mole ratio of 1:2 into an iron salt solution of a concentration of 0.5 mol/L, a nano-TiO2 was formulated into 10 wt % of TiO2 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.
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 Fe3O4 colloid solution. The TiO2 colloid was added in the Fe3O4 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 Fe3O4/TiO2. 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 Li4Ti5O12. 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 Li2.2Ti5O12. In this case, the particle size of the magnetic core Fe3O4 was 90 nm, the thickness of the TiO2 layer was 10 nm, and the thickness of the Li2.2Ti5O12 layer was 30 nm.
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.
The lithium salt solution was selected from a lithium chloride solution of a concentration of 2 mol/L.
The titanium salt solution was selected from a metatitanic acid solution of a concentration of 2 mol/L.
The calcining was carried out at 400° C. for 5 h.
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.
The concentration of the TiO2 colloid was 20 wt %.
The TiO2 colloid was added into the Fe3O4 colloid in a titanium-iron mole ratio of 1:2. The thickness of the TiO2 layer was 20 nm.
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.
The concentration of the TiO2 colloid was 5 wt %.
The TiO2 colloid was added into the Fe3O4 colloid in a titanium-iron mole ratio of 1:6. The thickness of the TiO2 layer was 2 nm.
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.
The concentration of the TiO2 colloid was 20 wt %.
The TiO2 colloid was added into the Fe3O4 colloid in a titanium-iron mole ratio of 1:1. The thickness of the TiO2 layer was 30 nm.
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.
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.
The thickness of the formed Li2.2Ti5O12 layer was 8 nm.
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.
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.
The thickness of the formed Li2.2Ti5O12 layer was 3 nm.
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.
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.
The thickness of the formed Li2.2Ti5O12 layer was 60 nm.
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.
Before the calcining, Mg(NO3)2 was added into the intermediate product particles for doping. Then, the lithium adsorption layer of the obtained magnetic titanium-based lithium adsorbent was Li2.2Ti4.9Mg0.1O12.
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.
Before the calcination, CoCO3 was added into the intermediate product particles for doping. Then, the lithium adsorption layer of the obtained magnetic titanium-based lithium adsorbent was Li2.2Ti4.9Co0.1O12.
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.
Before the calcining, Zn(NO3)2 was added into the intermediate product particles for doping. Then, the lithium adsorption layer of the obtained magnetic titanium-based lithium adsorbent was Li2.2Ti4.9Zn0.1O12.
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 5 nm.
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 0.3 nm.
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.
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, 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.
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 calcination, Li2O was added into the precursor of the magnetic titanium-based lithium adsorbent and then calcined again for coating. The thickness of the outermost Li2O coating layer was 5 nm.
This comparative example provides a magnetic manganese-based lithium adsorbent and a preparation method thereof, including the following steps:
Fe3O4 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 Fe3O4/SiO2 composite. The Fe3O4/SiO2 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.
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.
A preparation method of a magnetic composite is as follows. Fe3O4 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 Fe3O4/SiO2 composite.
By replacing the magnetic composite Fe3O4/TiO2 in Example 1, the Fe3O4/SiO2 composite was used for subsequent steps.
Performance Test
The above prepared magnetic titanium-based lithium adsorbents and magnetic manganese-based lithium adsorbent were subjected to the following performance tests.
Adsorption Performance Test:
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+ 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+ concentration after adsorption, Li+ adsorption capacity, Li+ 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+ adsorption capacity shown in Table 1.
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.
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.
It can be learned from the test results of Examples 1 and 3-5 that the thickness of the TiO2 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 TiO2 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.
It can be learned from the test results of Examples 1 and 6-8 that when the thickness of the Li4-xTi5O12 layer is within 5-50 nm, the magnetic titanium-based lithium adsorbent has a good lithium adsorption capacity and maintains a good saturation magnetization.
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.
It can be learned from the test results of Example 1 and Comparative Example 2 that TiO2 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+ adsorption performance after multiple times of use.
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.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202111567446.9 | Dec 2021 | CN | national |
