Method for extracting magnesium and lithium and producing layered double hydroxide from brine
10016727 ยท 2018-07-10
Assignee
Inventors
Cpc classification
C01F7/784
CHEMISTRY; METALLURGY
C01P2002/72
CHEMISTRY; METALLURGY
International classification
Abstract
The present invention relates to a method for extracting magnesium and lithium and also producing layered double hydroxides (LDH) from brine, comprising the steps of: adding an aluminum salt to brine, to prepare a mixed salt solution A for preparing MgAl-LDH; adding an alkaline solution to carry out co-precipitation, followed by crystallization; after the crystallization is complete, performing solid-liquid separation to obtain a solid product of MgAl-LDH and a filtrate; concentrating the filtrate by evaporation to obtain a lithium-rich brine, adding an aluminum salt thereto to prepare a mixed salt solution B for preparing LiAl-LDH; adding the mixed salt solution B to an alkaline solution to carry out precipitation; after the precipitation is complete, performing solid-liquid separation to obtain a solid product of LiAl-LDH and a filtrate; and concentrating the filtrate by evaporation, returning the solution concentrated by evaporation to the lithium-rich brine for recycled use. This method uses mild reaction and simple equipment, has a small loss of Li, can achieve isolation of resources from salt lakes, and can also obtain functional materials having a high added value.
Claims
1. A method for extracting magnesium and lithium and also producing layered double hydroxides (LDH) from brine, characterized in that the method comprises the steps of: adding an aluminum salt to brine, to prepare a mixed salt solution A for preparing MgAl-LDH; adding an alkaline solution to carry out co-precipitation, followed by crystallization; after the crystallization is complete, performing solid-liquid separation to obtain a solid product of MgAl-LDH and a filtrate; concentrating the filtrate by evaporation to obtain a lithium-rich brine, adding an aluminum salt thereto to prepare a mixed salt solution B for preparing LiAl-LDH; adding the mixed salt solution B to an alkaline solution to carry out precipitation; after the precipitation is complete, performing solid-liquid separation to obtain a solid product of LiAl-LDH and a filtrate; and concentrating the filtrate obtained in step b) by evaporation, returning the solution concentrated by evaporation to the lithium-rich brine in step b) for recycled use.
2. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the brine in step a) is brine from a sulfate-type salt lake which is rich in Li.sup.+, Mg.sup.2+, K.sup.+ and Na.sup.+, at concentrations of [Li.sup.+]=1 to 3 g/L, [Mg.sup.2+]=10 to 30 g/L, [K.sup.+]=5 to 7 g/L, and [Na.sup.+]=70 to 90 g/L.
3. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the brine in step a) is filtered to remove insoluble impurities prior to use.
4. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that, in the mixed salt solution A for preparing MgAl-LDH in step a), the total concentration of metal ions is 0.9 to 1.5 mol/L.
5. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that, in the mixed salt solution A for preparing MgAl-LDH in step a), the molar ratio of magnesium salt to aluminum salt is 2 to 4:1.
6. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the alkaline solution in step a) is a mixed solution of sodium hydroxide and sodium carbonate, having the same volume as the mixed salt solution A, wherein the number of moles of sodium hydroxide is 1.5 to 2.5 times the total number of moles of magnesium and aluminum elements, and the molar ratio of sodium carbonate to aluminum element is 1.5 to 2.5:1.
7. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the co-precipitation in step a) is carried out by mixing the mixed salt solution A for preparing MgAl-LDH with the alkaline solution, and spinning them at 1000 to 5000 rpm for 1 to 10 min, to obtain crystal nuclei of MgAl-LDH.
8. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the crystallization in step a) is carried out by allowing the crystal nuclei of MgAl-LDH obtained from the co-precipitation in step a) to react under stirring at 60 to 90 C. for 6 to 24 hours, and after the reaction is complete, performing solid-liquid separation to obtain a filter cake of MgAl-LDH.
9. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that, when a filter cake of MgAl-LDH is obtained in step a), the filter cake is dried to obtain a solid product of MgAl-LDH, wherein the drying is performed at 60 to 80 C. for 6 to 12 hours.
10. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the solid product of MgAl-LDH obtained in step a) has a chemical formula of [Mg.sup.2+.sub.1xAl.sup.3+.sub.x(OH).sub.2](CO.sub.3.sup.2).sub.x/2.nH.sub.2O, wherein x=0.2 to 0.4 and n=1 to 10.
11. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the lithium-rich brine in step b) has lithium ions at a concentration of 0.1 to 0.5 g/L.
12. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that, in the mixed salt solution B for preparing LiAl-LDH in step b), the molar ratio of lithium to aluminum is 1 to 6:1.
13. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the alkaline solution in step b) has a pH of 9 to 12, and includes an aqueous solution of sodium hydroxide or potassium hydroxide.
14. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the alkaline solution in step b) has the same volume as the mixed salt solution B for preparing LiAl-LDH, and the number of moles of sodium hydroxide or potassium hydroxide is 1 to 1.6 times the total number of moles of lithium and aluminum elements.
15. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the co-precipitation in step b) is carried out by dropwise adding the mixed salt solution B for preparing LiAl-LDH to the alkaline solution for co-precipitation, and after the co-precipitation is complete, performing solid-liquid separation to obtain a filter cake of LiAl-LDH; wherein the speed of the dropwise adding is 1 to 5 ml/min; the pH for the co-precipitation is 9 to 12, the temperature for the co-precipitation is 10 to 25 C., and the duration of the co-precipitation is 8 to 24 hours.
16. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that, when a filter cake of LiAl-LDH is obtained in step b), the filter cake is dried to obtain a solid product of LiAl-LDH, wherein the drying is performed at 60 to 80 C. for 6 to 12 hours.
17. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the solid product of LiAl-LDH obtained in step b) has a chemical formula of [LiAl.sub.2(OH).sub.6].sub.2CO.sub.3.nH.sub.2O, wherein n=1 to 10.
18. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the aluminum salt in step a) is one of aluminum nitrate, aluminum sulfate, and aluminum chloride.
19. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the aluminum salt in step b) is one of aluminum nitrate, aluminum sulfate, and aluminum chloride.
20. The method for extracting magnesium and lithium and also producing LDH from brine according to claim 1, characterized in that the concentrating by evaporation in step c) is concentrating the filtrate obtained in step b) by evaporation to a lithium ion concentrating of 0.1 to 0.5 g/L.
Description
DESCRIPTION OF DRAWINGS
(1)
(2)
(3)
(4)
(5)
DETAILED DESCRIPTION OF INVENTION
(6) In order to provide a better understanding of the technical features, objectives and beneficial effects of the present invention, the embodiments of the present invention and the beneficial effects produced thereby will be described in detail below in conjunction with specific examples and figures, to help readers better understand the spirit and features of the present invention, but the scope of the present invention is not limited thereto.
(7) The brine used in the example of the present invention was taken from the West Taijinar Salt Lake, and was sulfate-type brine, the composition of which is shown in Table 1 below. The process flow of the method for extracting Mg and Li from brine and also producing LDH as provided according to the present invention is shown in
(8) TABLE-US-00001 TABLE 1 Ion Na.sup.+ K.sup.+ Li.sup.+ Mg.sup.2+ Cl.sup. SO.sub.4.sup.2 Concentration 70-90 5-7 1-3 10-30 140-160 20-40 (g/L)
Example 1
(9) This Example provides a method for extracting Mg and Li from brine and also producing LDH, comprising the steps of: a) 26.0325 g MgCl.sub.2.6H.sub.2O, 25.7993 g MgSO.sub.4.7H.sub.2O, 18.7290 g AlCl.sub.3.6H.sub.2O, 3.3873 g KCl, 1.8768 g LiCl, and 8.068 g NaCl were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain a mixed salt solution A; 19.8593 g NaOH and 16.4443 g NaCO.sub.3 were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain an alkaline solution;
(10) the mixed salt solution A and the alkaline solution were added together to a colloid mill, and spun at 3000 rpm for 3 min to form crystal nuclei of MgAl-LDH; the crystal nuclei liquid was transferred to a reactor to carry out crystallization under dynamic stirring at 80 C. for 12 hours to grow MgAL-LDH; a filter cake of MgAl-LDH was obtained by filtration, and was dried at 70 C. for 12 hours to obtain a white solid product of MgAl-LDH, and the filtrate was collected in a container; the formula of the MgAl-LDH is [Mg.sub.0.75Al.sub.0.25(OH).sub.2](CO.sub.3.sup.2).sub.0.125.5H.sub.2O;
(11) b) the filtrate obtained in step a) was concentrated by evaporation at 50 C. to 250 ml wherein the lithium ion concentration reached 0.4432 g/L; 1.2847 g AlCl.sub.3.6H.sub.2O was added thereto to prepare a mixed salt solution B; 16.784 g NaOH was separately weighed and dissolved in 100 ml deionized water to a molar concentration of 4 mol/l; the mixed salt solution B was added dropwise to the sodium hydroxide solution at a speed of 1 ml/min, while the pH was maintained at 11, the co-precipitation was allowed to proceed at 20 C. for 12 hours, followed by filtration, and the filter cake was dried at 80 C. for 10 hours, to obtain a solid product of LiAl-LDH, which has a formula of [LiAl.sub.2(OH).sub.6].sub.2CO.sub.3.5H.sub.2O; and
(12) c) the filtrate obtained in step b) was concentrated by evaporation to [Li.sup.+]=0.3 g/L, and the concentrate was returned to step b) for recycled use.
(13) The MgAl-LDH product prepared in Example 1 was analyzed by X-ray diffraction and transmission electron microscopy (TEM), to obtain an X-ray diffraction spectrum as shown in
(14) The LiAl-LDH product prepared in Example 1 was analyzed by X-ray diffraction and scanning electron microscopy (SEM), to obtain an X-ray diffraction spectrum as shown in
Example 2
(15) a) 39.0487 g MgCl.sub.2.6H.sub.2O, 38.6989 g MgSO.sub.4.7H.sub.2O, 32.7187 g Al(NO.sub.3).sub.3.9H.sub.2O, 9.1837 g KCl, 1.8768 g LiCl, and 8.068 g NaCl were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain a mixed salt solution A; 22.3368 g NaOH and 16.4443 g NaCO.sub.3 were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain an alkaline solution;
(16) the mixed salt solution A and the alkaline solution were added together to a colloid mill, and spun at 4000 rpm for 5 min to form crystal nuclei of MgAl-LDH; the crystal nuclei liquid was transferred to a reactor to carry out crystallization under dynamic stirring at 80 C. for 12 hours to grow MgAL-LDH; a filter cake of MgAl-LDH was obtained by filtration, and was dried at 80 C. for 6 hours to obtain a white solid product of MgAl-LDH, and the filtrate was collected in a container; the formula of the MgAl-LDH is [Mg.sub.0.8Al.sub.0.2(OH).sub.2](CO.sub.3.sup.2).sub.0.1.6H.sub.2O;
(17) b) the filtrate obtained in step a) was concentrated by evaporation at 50 C. to 250 ml wherein the lithium ion concentration reached 0.4385 g/L; 1.9749 g Al(NO.sub.3).sub.3.9H.sub.2O was added thereto to prepare a mixed salt solution B; 16.784 g NaOH was separately weighed and dissolved in 100 ml deionized water to a molar concentration of 4 mol/l; the mixed salt solution B was added dropwise to the sodium hydroxide solution at a speed of 2 ml/min, while the pH was maintained at 11, the co-precipitation was allowed to proceed at 20 C. for 12 hours, followed by filtration, and the filter cake was dried at 70 C. for 12 hours, to obtain a solid product of LiAl-LDH, which has a formula of [LiAl.sub.2(OH).sub.6].sub.2CO.sub.3.3H.sub.2O; and
(18) c) the filtrate obtained in step b) was concentrated by evaporation to [Li.sup.+]=0.4 g/L, and the concentrate was returned to step b) for recycled use.
Example 3
(19) a) 39.0487 g MgCl.sub.2.6H.sub.2O, 29.139 g MgSO.sub.4.7H.sub.2O, 71.2620 g Al.sub.2(SO.sub.4).sub.3.18H.sub.2O, 9.1837 g KCl, 1.8768 g LiCl, and 8.068 g NaCl were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain a mixed salt solution A; 22.3223 g NaOH and 16.4443 g NaCO.sub.3 were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain an alkaline solution;
(20) the mixed salt solution A and the alkaline solution were added together to a colloid mill, and spun at 2000 rpm for 6 min to form crystal nuclei of MgAl-LDH; the crystal nuclei liquid was transferred to a reactor to carry out crystallization under dynamic stirring at 70 C. for 10 hours to grow MgAL-LDH; a filter cake of MgAl-LDH was obtained by filtration, and was dried at 80 C. for 8 hours to obtain a white solid product of MgAl-LDH, and the filtrate was collected in a container; the formula of the MgAl-LDH is [Mg.sub.0.744Al.sub.0.256(OH).sub.2](CO.sub.3.sup.2).sub.0.128.4H.sub.2O;
(21) b) the filtrate obtained in step a) was concentrated by evaporation at 50 C. to 250 ml wherein the lithium ion concentration reached 0.4108 g/L; 1.6435 g Al.sub.2(SO.sub.4).sub.3.18H.sub.2O was added thereto to prepare a mixed salt solution B; 16.784 g NaOH was separately weighed and dissolved in 100 ml deionized water to a molar concentration of 4 mol/l; the mixed salt solution B was added dropwise to the sodium hydroxide solution at a speed of 3 ml/min, while the pH was maintained at 10.5, the co-precipitation was allowed to proceed at 20 C. for 12 hours, followed by filtration, and the filter cake was dried at 70 C. for 12 hours, to obtain a solid product of LiAl-LDH, which has a formula of [LiAl.sub.2(OH).sub.6].sub.2CO.sub.3.6H.sub.2O; and
(22) c) the filtrate obtained in step b) was concentrated by evaporation to [Li.sup.+]=0.2 g/L, and the concentrate was returned to step b) for recycled use.
Example 4
(23) a) 39.0487 g MgCl.sub.2.6H.sub.2O, 38.6989 g MgSO.sub.4.7H.sub.2O, 32.6363 g Al(NO.sub.3).sub.3.9H.sub.2O, 3.3873 g KCl, 1.8768 g LiCl, and 8.068 g NaCl were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain a mixed salt solution A; 33.472 g NaOH and 18.4422 g NaCO.sub.3 were weighed out and dissolved in deionized water, and the volume thereof was metered in a 250 ml volumetric flask to obtain an alkaline solution;
(24) the mixed salt solution A and the alkaline solution were added together to a colloid mill, and spun at 3000 rpm for 3 min to form crystal nuclei of MgAl-LDH; the crystal nuclei liquid was transferred to a reactor to carry out crystallization under dynamic stirring at 80 C. for 24 hours to grow MgAL-LDH; a filter cake of MgAl-LDH was obtained by filtration, and was dried at 70 C. for 10 hours to obtain a white solid product of MgAl-LDH, and the filtrate was collected in a container; the formula of the MgAl-LDH is [Mg.sub.0.8Al.sub.0.2(OH).sub.2](CO.sub.3.sup.2).sub.0.1.7H.sub.2O;
(25) b) the filtrate obtained in step a) was concentrated by evaporation at 50 C. to 250 ml wherein the lithium ion concentration reached 0.4573 g/L; 1.3256 g AlCl.sub.3.6H.sub.2O was added thereto to prepare a mixed salt solution B; 16.784 g NaOH was separately weighed and dissolved in 100 ml deionized water to a molar concentration of 4 mol/l; the mixed salt solution B was added dropwise to the sodium hydroxide solution at a speed of 5 ml/min, while the pH was maintained at 12, the co-precipitation was allowed to proceed at 20 C. for 12 hours, followed by filtration, and the filter cake was dried at 60 C. for 12 hours, to obtain a solid product of LiAl-LDH, which has a formula of [LiAl.sub.2(OH).sub.6].sub.2CO.sub.3.7H.sub.2O; and
(26) c) the filtrate obtained in step b) was concentrated by evaporation to [Li.sup.+]=0.4 g/L, and the concentrate was returned to step b) for recycled use.