Pyrometallurgical method for obtaining compounds of lithium and intermediates from alpha-spodumene and lepidolite

Abstract

Pyrometallurgic process for obtaining lithium compounds and intermediates, the process being characterized by comprising the steps of a) contacting lithium aluminosilicate particles with at least a fluorine solid compound, b) heating until a temperature of 25 to 900° C. obtaining a solid mixture and c) carrying out at least a leaching process of the mixture in step b).

Claims

1. Pyrometallurgic process to obtain lithium compounds and intermediaries, comprising the steps of a) contacting particles of at least a lithium aluminosilicate with at least a solid fluorine solid compound, selected from the group consisting of NaF, KF or NH.sub.4HF.sub.2; b) heating until a temperature of 120° C. to 900° C. obtaining as a product of the reaction a solid mixture comprising at least a compound of the group consisting in lithium fluoride (LiF), albite (NaAlSi.sub.3O.sub.8), nepheline (NaAlSiO.sub.4), leucite (KAlSi.sub.2O.sub.6), aluminum fluoride (AlF.sub.3) and ammonium hexafluorosilicate ((NH.sub.4).sub.3SiF.sub.6); c) carrying out a leaching process with distilled water of the mixture of step b) to eliminate excess fluorinating agent, NaF, KF or NH.sub.4HF.sub.2, and subsequently filter and dry; and d) carrying out at least the leaching process of the solid mixture obtained in step c) using as leaching agents compounds selected from the group consisting of sodium hydroxide (NaOH), calcium chloride (CaCl.sub.2), sulfuric acid (H.sub.2SO.sub.4) and subsequently filter and dry.

2. Process according to claim 1, wherein at least a lithium aluminosilicate is α-spodumene, lepidolite or a combination thereof.

3. Process according to claim 1, wherein in step a) the aluminosilicate particles comprise a size between 29 and 200 μm.

4. Process according to claim 1, wherein the heating of step b) is carried out for a time of 30 to 300 min.

5. Process according to claim 1, wherein the fluorine solid compound is NaF, and the molar ratio aluminosilicate:NaF is between 1:1 and 1:2.5.

6. Process according to claim 1, wherein the fluorine solid compound is KF, and the molar ratio aluminosilicate:KF is between 1:1 and 1:2.5.

7. Process according to claim 1, wherein the fluorine solid compound is NH.sub.4HF.sub.2, and the molar ratio aluminosilicate:NH.sub.4HF.sub.2 is between 1:3.0 and 1:19.

Description

DESCRIPTION OF THE DRAWINGS

(1) For greater clarity and comprehension of the present invention, it has been illustrated with various figures, wherein the preferred embodiment has been represented, as an example, wherein:

(2) FIG. 1a) illustrates the DT-FGA curve of the α-spodumene:NaF mixture in molar ratio 1:1.5.

(3) FIG. 1b) shows a phase diagram for the NaF—LiF mixture.

(4) FIG. 2 shows the X-ray diffractograms. a) α-spodumene:NaF mixture in molar ratio 1:2. b) calcined at ratio 1:2 at 500° C., 120 min. c) calcined at ratio 1:2 at 800° C., 120 min.

(5) FIG. 3 shows the effect of temperature of the α-spodumene:KF system.

(6) FIG. 4 shows X-ray diffractograms. a) Calcined in molar ratio 1:2 at 500° C., 120 min. b) Calcined in ratio 1:2 at 600° C., 120 min. c) Calcined in ratio 1:2 at 700° C., 120 min. d) Calcined in ratio 1:2 at 800° C., 120 min.

(7) FIG. 5 shows the effect in molar ratio of α-spodumene:NaF during a 2 hs calcination at 700° C.

(8) FIG. 6 shows the effect in molar ratio α-spodumene:KF during a 2 hs calcination at 700° C.

(9) FIG. 7 shows the calcination time effect at 700° C. α-spodumene:NaF mixture in molar ratio 1:2.

(10) FIG. 8 shows X-ray diffractograms. a) α-spodumene:NaF mixture at molar ratio 1:2. b) Calcined at ratio 1:2 at 700° C., 30 min. c) Calcined at ratio 1:2 at 700° C., 60 min. d) Calcined at ratio 1:2 at 700° C., 180 min.

(11) FIG. 9 shows the calcination time effect at 700° C. in α-spodumene:KF mixture at molar ratio 1:2.

(12) FIG. 10 shows the effect at molar ratio of α-spodumene:NH.sub.4HF.sub.2 during a 2 hs calcination at 230° C.

(13) FIG. 11 shows the effect of the leaching agent on Li extraction at different times for the calcine obtained from the α-spodumene:NaF mixture at 700° C. during 2 hours with a molar ratio 1:2.

(14) FIG. 12 shows the effect of H.sub.2SO.sub.4 on Li extraction for the calcine obtained from the α-spodumene:NaF mixture at 700° C. during 2 hours with a molar ratio 1:2.

(15) FIG. 13 shows the flow chart for the process using NaF with α-spodumene.

(16) FIG. 14 shows the flow chart for the process using KF with α-spodumene.

(17) FIG. 15 shows the flow chart for the process using (NH.sub.4)HF.sub.2 with α-spodumene.

(18) FIG. 16 shows the flow chart for the process using NaF with lepidolite.

(19) FIG. 17 shows the flow chart for the process using KF with lepidolite.

(20) FIG. 18 shows the flow chart for the process using NH.sub.4HF.sub.2 with lepidolite.

DETAILED DESCRIPTION OF THE EMBODIMENT EXAMPLE

(21) For the direct fluoridation process of lithium aluminosilicates for lithium fluoride synthesis, the following tests are described:

(22) Calcination Test

(23) 7 g of α-spodumene, or lepidolite with NaF, KF or NH.sub.4HF.sub.2 mixtures at different molar ratio were prepared for the experimental tests in a manual mortar during 5 minutes. Each mixture was placed in a porcelain crucible and calcined in a muffle with temperature control between 120 and 900° C. Next the calcined solid was pulverized in a manual mortar during 5 minutes. Then, 2 g therein were leached during an hour with distilled water at 25° c. in a PVC reactor with continuous stirring. Finally the leaching solution was filtered and dried to be analyzed.

(24) The extraction reaction was quantified by calculating the amount of XF (X: Na o K o NH.sub.4) that reacts with the mineral using the following equation:
XF.sub.(C)-XF.sub.(L)=XF.sub.(R)  (1)
wherein
XF.sub.(C): Amount of calcined XF.
XF.sub.(L): Amount of XF in the leaching
XF.sub.(R): Amount of XF reacting with the mineral
Using the amount of reacted XF, according to equation (2.a), allows to calculate the amount of Li extracted from the mineral.
From the thermodynamic analysis results the following reactions are provided for the different reaction systems:
LiAlSi.sub.2O.sub.6+NaF.fwdarw.LiF+NaAlSi.sub.2O.sub.6  (2.a)
2NaAlSi.sub.2O.sub.6.fwdarw.NaAlSi.sub.3O.sub.8+NaAlSiO.sub.4  (2.b)
NaAlSi.sub.3O.sub.8+NaAlSiO.sub.4+2SiO.sub.2  (2.c)
LiAlSi.sub.2O.sub.6+KF.fwdarw.LiF+KAlSi.sub.2O.sub.6  (3)
Li.sub.2O.Al.sub.2O.sub.3.4SiO.sub.2+19(NH.sub.4)HF.sub.2.fwdarw.2LiF+4(NH.sub.4).sub.2SiF.sub.6+2(NH.sub.4).sub.3AlF.sub.6+5NH.sub.3+12H.sub.2O  (4.a)
(NH.sub.4).sub.3AlF.sub.6.fwdarw.AlF.sub.3+3NH.sub.4F  (4.b)

(25) Effect of the α-spodumene:NaF temperature

(26) In FIG. 1 differential thermal analysis results have been shown, wherein the endothermic peak noted between 500 and 600° C. is due to the beginning of the reaction between the mineral and NaF, while the exothermic peak noted between 650 and 750° C. matches with formation of an eutectic between NaF and (generated) LiF, FIG. 1b

(27) The comparative results of DRX analysis of the non-calcined mixture and those calcined at 500, 600, 700 and 800° C. are shown in FIG. 2. In FIG. 2a the diffraction pattern is noted corresponding to α-spodumene (JCPDS 33-0786) and sodium fluoride (ICDD 01-088-2299) and quartz (JCPDS 33-1161) present as a bargain. In the calcined mixtures at 500 and 600° C. (FIGS. 2b and c) a decrease can be noticed in the intensity of the diffraction lines of α-spodumene, relative to diffractogram of the non-reacted mixture, which would indicate the beginning of the mineral reaction. In FIG. 2d) and e), corresponding to 700 and 800° C. the nearly complete disappearance can be noticed of α-spodumene phase and formation of LiF, albite (NaASi.sub.3O.sub.8), and nepheline (NaAlSiO.sub.4). This data confirms the proposed reactions by thermodynamic study.

(28) Effect of the α-Spodumene:KF Temperature

(29) The study carried out on the temperature on the thermodynamic behavior of the α-spodumene:KF system was performed with the HSC Chemistry 5.11 program. The results are shown in FIG. 3.

(30) From FIG. 3 one can infer that the reaction is thermodynamically favored in all the proposed temperature ranges (25-800° C.) with conditions of maximum extraction in the range corresponding between 600 and 800° C.

(31) FIG. 4 shows the diffractograms of the solids obtained. In the calcines mixtures at 500 and 600° C. (FIGS. 4b) and 4c)) a decrease in intensity of the α-spodumene diffraction lines can be observed, relative to the diffractogram of the non-reacted mixture, which would indicate the beginning of the mineral reaction. Further, from 600° C. appearance of leucite compound is detected. In FIG. 2d) and e), corresponding to 700 and 800° C. nearly complete of the disappearance of α-spodumene phase can be observed and formation of LiF and leucite (KAlSi.sub.2O.sub.6). This data confirms the proposed reactions by thermodynamic studies.

(32) Effect of the α-Spodumene:NaF Molar Ratio

(33) FIG. 5, shows the results obtained from studying the effect exerted addition of NaF on the mineral conversion. The α-spodumene:KF mixtures with molar ratios of 1:1, 1:1.3; 1:1.6 and 1:2 were calcined at 700° C. during 2 hours and then leached with water during an hour at 25° C. and constant stirring.

(34) The curve shows that the higher Li extractions were reached which higher KF amounts to the stoichiometric relation raised in equation 3, obtaining extractions of 95 and 97% with molar ratios of 1:1.3 and 1:2, respectively.

(35) Effect of α-Spodumene:NaF Calcination Time

(36) The results obtained from studying the effect of calcination time on the mineral conversion with NaF, is shown in FIG. 7. The α-spodumene:NaF mixtures with molar ratio 1:2 were calcined at 700° C. during 30, 60, 90, 120, 180 and 240 minutes and later, leached with water during an hour at 25° C. and constant stirring.

(37) The curve obtained shows that upon increasing the calcination time, an increase in the amount of extracted Li is produced; this can be explained taking into account that upon increasing the contact time between the solids favors the ionic exchange reaction between Na+ from NaF and Li+ of the mineral. Once having reached 120 min, this effect is nearly negligible.

(38) FIG. 8, comparatively shows the analysis results with DRX of the molar ratio 1:2 α-spodumene:NaF mixtures, without being calcined and calcined at 700° C. during 30, 60, 120 and 189 minutes. In the corresponding diffractogram to the mixture calcined for 30 minutes (FIG. 8b) one can notice a pronounced decrease in the intensity of the α-spodumene peaks as regards the non-reacted mixture (FIG. 8a) and appearance of the LiF corresponding diffraction pattern. In FIG. 8c) corresponding to 60 minutes calcination, the albite (NaAlSi.sub.3O.sub.8), nepheline (NaAlSiO.sub.4) and lithium fluoride (LiF) phases can be noticed, with a decrease in the α-spodumene diffraction lines; while in FIG. 8d) and e) nearly complete disappearance of the α-spodumene phase can be seen, while the LiF, albite and nepheline phases show a greater intensity as regards their diffraction lines, indicating that the reaction of the mineral with NaF has been complete.

(39) Effect of α-Spodumene:KF Calcination Time

(40) The results obtained from studying the calcination time effect on the mineral conversion with KF is observed in FIG. 9. The α-spodumene:KF mixtures with molar ratio 1:2 were calcined at 700° C. during 30, 60, 90, 120, 180, 240 and 300 minutes and then leached with water during an hour at 25° C. and constant stirring.

(41) The curve obtained shows that by increasing calcination time, an increase in the amount of extracted Li is produced, this can be explained taking into account that by increasing the contact time between the solids favors the ionic interchange reaction between K+ from KF and Li from the mineral. Once having reached 120 min, this effect is nearly negligible.

(42) Effect of α-Spodumene:NH.sub.4HF.sub.2 Molar Ratio

(43) FIG. 10 shows the results obtained from studying the effect of adding NH.sub.4HF.sub.2 on the mineral conversion. The α-spodumene:NH.sub.4HF.sub.2 mixtures with molar ratios of 1:3.5; 1:9.5 and 1:19 were calcined at 230 during two hours and later, leached with water during one hour at 25° C.

(44) The curve shows that the greater Li extractions were reached with amounts of NH.sub.4HF.sub.2 in the stoichiometric relationship raised in equation 4a, obtaining extractions of 65% with molar ratios of 1:9.5 and 1:19, respectively

(45) Li Extraction Tests

(46) From the results obtained in the previous step tests were carried out to extract Li from the α-spodumene:NaF or KF (molar ratio 1:2, 120 min, 700° C.) and α-spodumene:NH.sub.4HF.sub.2 (molar ratio 1:9.5, 120 min, 230° C.) samples. Please note that, these calcination conditions were selected as optimum for said step. Next, the results for the mineral with NaF mixture are shown.

(47) The operative variables studied were, leaching agent, agent concentration and leaching time.

(48) Effect of the Leaching Agent

(49) From studying the effect that the leaching agent exert and the reaction time on Li extraction at different times, was carried out using the following working conditions: 300 ml leaching solution (total volume) and 14 g of α-spodumene:NaF (1:2) mixture, calcined at 700° C. during 120 min. The tested leaching agents were water and solutions of: CaCl.sub.2 0.09 M at pH7, CaCl.sub.2 0.09 M at pH 13 and H.sub.2SO.sub.4 at 10% v/v. The leaching time interval was from 30 to 240 min. The results of this study are shown in FIG. 10.

(50) In FIG. 11 you may note that the best extraction values are reached using H.sub.2SO.sub.4 solutions, a strong difference is detected between tis one and the other agents used. The maximum extraction obtained was 92.5% working with H.sub.2SO.sub.4 at 10% v/v at a time of 90 min. in all the experiments we have noticed that the reaction time does not have a strong influence on the extraction reaction. From these results, H.sub.2SO.sub.4 was selected as the leaching agent for future studies.

(51) Effect of the Leaching Agent Concentration

(52) Investigation of H.sub.2SO.sub.4 concentration effect on Li extraction at different reaction times, was carried out using a total volume leaching solution of 300 ml and 14 g α-spodumene:NaF (1:2) mixture, calcined at 700° C. during 2 hours. The concentrations of leaching agent studied were: between 3, 5 and 10% v/v for a time interval compressed between 30 and 240 min. The results are shown in FIG. 12.

(53) In FIG. 12 shows that upon decreasing the concentration of H.sub.2SO.sub.4 a decrease in the Li extraction percentage is not detected. The maximum extraction achieved was 98% working with 5% H.sub.2SO.sub.4. In all the experiments the reaction time does not have a strong influence on the extraction reaction should be noted.

EXAMPLES

Example 1 (α-Spodumene:NaF)

(54) 142.85 g α-spodumene (6.5% Li.sub.2O) and 57.15 g sodium fluoride were mixed (molar ratio 1:2, respectively) during 15 minutes in rod mills. Then, the solid mixture was placed in a ceramic crucible and calcined during 2 hours at 700° C., in a muffle, obtaining a LiF formation or mineral conversion at 91%. Next, the calcined sample was leached during one hour with 600 mL sulfuric acid solution at 10% v/v. Afterwards, the mixture was filtered separating the solid residues from the leaching solution, at the latter the lithium was quantified by flame photometry, obtaining a total value of lithium extraction of 85%.

Example 2 (α-Spodumene:NaF)

(55) 136.06 g α-spodumene (6.5% Li.sub.2O) and 63.94 g sodium fluoride were mixed (molar ratio 1:2) during 15 minutes in rod mills. Then, the solid mixture was placed in a ceramic crucible and calcined during 2 hours at 700° C., in a muffle, obtaining a conversion of 92%. Next, the calcined sample was leached during one hour with 600 mL sulfuric acid solution at 20% v/v. Finally, filtered separating the solid residues from the lithium solution and determined thereof by flame photometry, obtaining a total lithium extraction of 89%.

Example 3 (α-Spodumene:NaF)

(56) 136.06 g α-spodumene (6.5% Li.sub.2O) and 63.94 g sodium fluoride were mixed (molar ratio 1:2) during 15 minutes in rod mills. Then, the solid mixture was placed in a ceramic crucible and calcined during 2 hours at 700° C., in a muffle, obtaining a conversion of 92%. Next, the calcined sample was leached during one hour with 600 mL sulfuric acid solution at 7.5%. Finally, the mixture was filtered separating the solid residues from the leaching solution. In the latter lithium was determined by flame photometry, obtaining a total lithium extraction of 68%.

Example 4 (α-Spodumene:KF)

(57) The mineral sample was milled in rod mills during 15 minutes. From this, 142.85 g α-spodumene (6.5% Li.sub.2O) and 57.15 g potassium fluoride were mixed (molar ratio 1:1.3) during 15 minutes in rod mills. Then, the solid mixture was placed in a ceramic crucible and calcined during 2 hours at 700° C., in a muffle, obtaining a conversion of 93%. Next, the calcined sample was leached during one hour with 600 mL sulfuric acid solution at 10% v/v. Finally, the mixture was filtered separating the solid residues from the leaching solution, in the latter lithium was determined by flame photometry, obtaining a total lithium extraction of 85%.

Example 5 (α-Spodumene:NH.SUB.4.HF.SUB.2

(58) 142 g α-spodumene (6.5% Li.sub.2O) and 409 g ammonium biflouride were mixed (molar ratio 1:9.5) during 15 in rod mills. Then, the solid mixture was placed in a ceramic crucible coated with aluminum and the content calcined during 2 hours at 230° C., in a muffle, to form LiF the mineral conversion was 95%. Next, the calcined sample was leached during one hour with 600 mL sulfuric acid solution at 10% v/v. Afterwards, the mixture from the previous step was filtered separating the solid residues from the leaching solution, in the latter lithium was quantified by flame photometry, obtaining a total lithium extraction value of 65%.

Example 6 (Lepidolite:NaF)

(59) 130 g lepidolite (4% Li.sub.2O) and 40 g sodium fluoride were mixed (molar ratio 1:2) during 15 minutes in rod mills. The solid mixture was placed in a ceramic crucible and calcined during 2 hours at 700° C., in a muffle, obtaining a conversion of 90%. Next, the calcined was leached during one hour with 600 mL sulfuric acid solution at 7.5%. Finally, the mixture was filtered separating the solid residues from the leaching solution, then in the latter lithium was determined by flame photometry, obtaining a total lithium extraction of 75%.

Example 7 (Lepidolite:KF)

(60) 130 g lepidolite (4% Li.sub.2O) and 50 g potassium fluoride were mixed (molar ratio 1:2) during 15 minutes in rod mills. The reactive mixture was placed in a ceramic crucible and calcined during 2 hours at 700° C., in a muffle, obtaining a conversion of 90%. Next, the calcined was leached during one hour with 600 mL sulfuric acid solution at 7.5%. Finally, the mixture was filtered separating the solid residues from the leaching solution, then in the latter lithium was determined by flame photometry, obtaining a total lithium extraction of 80%.

Example 8 (Lepidolite:NH.SUB.4.HF.SUB.2

(61) 130 g lepidolite (4% Li.sub.2O) and 450 g ammonium biflouride were mixed (molar ratio 1:9.5) during 15 in rod mills. The reactive mixture was placed in a ceramic crucible coated with aluminum and calcined during 2 hours at 230° C., in a muffle, obtaining a conversion of 90%. Next, the calcined was leached during one hour with 600 mL sulfuric acid solution at 7.5%. Finally, the mixture was filtered separating the solid residues from the leaching solution, then in the latter lithium was determined by flame photometry, obtaining a total lithium extraction of 86%.