Method for continuously preparing mixed hydroxide precipitate from laterite nickel ore by hydrometallurgy
12391574 ยท 2025-08-19
Assignee
- PT QMB NEW ENERGY MATERIALS (Jakarta, ID)
- PT ESG NEW ENERGY MATERIAL (Jakarta, ID)
- GEM CO., LTD. (Shenzhen, CN)
- PT GEM INDONESIA NEW ENERGY MATERIALS (Jakarta, ID)
Inventors
- Kaihua XU (Shenzhen, CN)
- SATRYO SOEMANTRI BRODJONEGORO (Jakarta, ID)
- TEGAR MUKTI AJI (Jakarta, ID)
- RIZKY WANALDI (Jakarta, ID)
- ANDI SYAPUTRA HASIBUAN (Jakarta, ID)
- EVAN WAHYU KRISTIYANTO (Jakarta, ID)
- EMIL SALIM (Jakarta, ID)
- TAO CUI (Jakarta, ID)
Cpc classification
C01P2004/61
CHEMISTRY; METALLURGY
Y02P10/20
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
International classification
Abstract
Disclosed is a method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy. Primary-precipitated mixed hydroxide precipitate particles are used as crystal nuclei, by controlling precipitation process conditions, the quantity of the crystal nuclei, and reaction time of the crystal nuclei, primary mixed hydroxide precipitate crystal nuclei gradually grow, and crystal forms become larger. By controlling the number of cycles, a proportion of returned seed crystals, and a homogenization ratio with precipitants, mixed hydroxide precipitate particles with narrow particle size distribution, dense particles, and better sedimentation effect are obtained, thereby reducing a moisture content of mixed hydroxide precipitate. The preparation method in this disclosure plays a certain guiding role in practical production and has good application prospects.
Claims
1. A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy, comprising the following steps: (1) firstly, taking a laterite nickel ore solution after removal of iron and aluminum, adding a precipitant for a precipitation reaction to form a primary-precipitated mixed hydroxide precipitate crystal nucleus precipitation solution, and then performing thickening to obtain a mixed hydroxide precipitate crystal nucleus slurry; (2) adding the precipitant to the mixed hydroxide precipitate crystal nucleus slurry for homogenization to obtain a homogenized crystal nucleus slurry mixture, and simultaneously adding the homogenized crystal nucleus slurry mixture, the precipitant, and the laterite nickel ore solution after removal of iron and aluminum into a reactor for a reaction to obtain a primary growing mixed hydroxide precipitate precipitation solution; (3) thickening the primary growing mixed hydroxide precipitate precipitation solution, and then adding the precipitant for a precipitation reaction to obtain a secondary growing mixed hydroxide precipitate precipitation solution; and (4) thickening the secondary growing mixed hydroxide precipitate precipitation solution, then adding the precipitant for a precipitation reaction to obtain a tertiary growing mixed hydroxide precipitate precipitation solution, taking obtaining one time of growing mixed hydroxide precipitate precipitation solution as a cycle and performing such cycle one or more times to obtain a final mixed hydroxide precipitate precipitation solution, and performing filtration, washing and drying to obtain mixed hydroxide precipitate particles; wherein, a mass ratio of the homogenized crystal nucleus slurry mixture, to the precipitant, to the laterite nickel ore solution after removal of iron and aluminum in Step (2) is (1-8):(1-4):100.
2. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 1, wherein the mixed hydroxide precipitate crystal nucleus slurry in Step (2) is homogenized in a mass ratio of the amount of the mixed hydroxide precipitate crystal nucleus slurry to a theoretical precipitation quantity being (6-10):1.
3. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 2, wherein a mass ratio of a slurry obtained by the thickening in Step (3) and Step (4) to the precipitant is (1-10):1.
4. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 1, wherein sources of the laterite nickel ore solution after removal of iron and aluminum in Step (1) and Step (2) are a solution obtained through high-pressure acid leaching of the laterite nickel ore and then removal of iron and aluminum.
5. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 4, wherein the precipitants in Steps (1)-(4) are at least one of sodium hydroxide, lime milk, potassium hydroxide, calcium oxide, magnesium oxide, and magnesium hydroxide.
6. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 5, wherein the sodium hydroxide is blended to obtain a solution with a concentration of 4-25 wt % during use, and a concentration of the lime milk is 5-30 wt %.
7. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 1, wherein conditions for the precipitation reaction in Step (1) are: temperature of 40-70 C. and time of 30 min-12 h.
8. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 7, wherein conditions for the reaction in Step (2) are: temperature of 40-70 C. and time of 1 min to 4 h.
9. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 8, wherein conditions for the precipitation reactions in Step (3) and Step (4) are: temperature of 40-70 C. and time of 30 min-12 h.
10. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 1, wherein the number of cycles in Step (4) is 1-20.
11. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 1, wherein filtration in Step (4) is performed through any one of a centrifuge, a vertical filter press and a horizontal filter press.
12. The method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy according to claim 1, wherein a washing manner in Step (4) is: during filtration, a filter cake is rinsed with water or water is added for dilution and washing.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
(2) In order to make the objectives and advantages of this disclosure clearer and more comprehensible, this disclosure is described in further detail below with reference to the embodiments. It should be understood that the specific embodiments described herein are merely illustrative of this disclosure and are not intended to limit this disclosure.
(3) The source of the laterite nickel ore solution after removal of iron and aluminum used in the embodiments and comparative embodiments is a solution obtained through high-pressure acid leaching of the laterite nickel ore and removal of iron and aluminum. Cationic components are as follows: nickel ions of 3.2 g/L, cobalt ions of 0.3 g/L, manganese ions of 2.4 g/L, and magnesium ions of 3.8 g/L.
Embodiment 1
(4) A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy includes the following steps:
(5) (1) firstly, 1 L of a laterite nickel ore solution after removal of iron and aluminum was taken, 21.6 g of a precipitant (sodium hydroxide with a concentration of 20 wt %) was added for a precipitation reaction (reaction temperature of 60 C., and time of 1 h) to form a primary-precipitated mixed hydroxide precipitate crystal nucleus precipitation solution, and then thickening for separation was performed to obtain a mixed hydroxide precipitate crystal nucleus slurry;
(6) (2) 10.8 g of a precipitant (sodium hydroxide with a concentration of 20 wt %) was added to 30 g of the mixed hydroxide precipitate crystal nucleus slurry for homogenization (5 min) to obtain a homogenized crystal nucleus slurry mixture; and the homogenized crystal nucleus slurry mixture, the precipitant (sodium hydroxide with a concentration of 20 wt %), and the laterite nickel ore solution after removal of iron and aluminum were taken in a mass ratio of 4:1:100, and were simultaneously added into a reactor for a reaction (reaction temperature of 60 C., and time of 1 h) to obtain a primary growing mixed hydroxide precipitate precipitation solution;
(7) (3) the primary growing mixed hydroxide precipitate precipitation solution was subjected to thickening for separation, and then the precipitant (sodium hydroxide with a concentration of 20 wt %, and a mass ratio of the precipitant to the slurry being 1:3) was added to the slurry obtained through separation for a precipitation reaction (reaction temperature of 60 C., and time of 1 h) to obtain a secondary growing mixed hydroxide precipitate precipitation solution; and
(8) (4) the secondary growing mixed hydroxide precipitate precipitation solution was subjected to thickening for separation, the precipitant (sodium hydroxide with a concentration of 20 wt %, and a mass ratio of the precipitant to the slurry being 1:4) was added to the slurry obtained through separation for a precipitation reaction (reaction temperature of 60 C., and time of 1 h) to obtain a tertiary growing mixed hydroxide precipitate precipitation solution, such cycle was performed 15 times (means that seed crystal growth in the mixed hydroxide precipitate precipitation solution repeats 15 times in total) to obtain a final mixed hydroxide precipitate precipitation solution, and filtration, washing and drying were performed to obtain mixed hydroxide precipitate particles.
(9) After detection, the mixed hydroxide precipitate particles prepared in Embodiment 1 have: D10=1.962 m, D50=6.915 m, and D90=15.434 m.
(10) The final mixed hydroxide precipitate precipitation solution obtained in Embodiment 1 has a moisture content of 53.2% after being subjected to filter pressing by the filter press. After detection and calculation, the mixed hydroxide precipitate particles prepared in Embodiment 1 contain 39.5% of nickel and 3.3% of cobalt, with a nickel-cobalt precipitation rate of 88%.
Embodiment 2
(11) A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy includes the following steps: the embodiment is different from Embodiment 1 only in that: the reaction time in Steps 1-4 should be 2 h, and the number of cycles in Step 4 should be 20.
(12) After detection, the mixed hydroxide precipitate particles prepared in Embodiment 2 have: D10=2.142 m, D50=7.225 m, and D90=15.736 m.
(13) The final mixed hydroxide precipitate precipitation solution obtained in Embodiment 2 has a moisture content of 51.8% after being subjected to filter pressing by the filter press.
(14) After detection and calculation, the mixed hydroxide precipitate particles prepared in Embodiment 2 contain 39.8% of nickel and 3.32% of cobalt, with a nickel-cobalt precipitation rate of 90%.
Embodiment 3
(15) A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy includes the following steps: the embodiment is different from Embodiment 1 only in that: the reaction time in Steps 1-4 is 4 h, and the number of cycles in Step 4 is 10.
(16) After detection, the mixed hydroxide precipitate particles prepared in Embodiment 3 have: D10=1.915 m, D50=7.153 m, and D90=15.582 m.
(17) The final mixed hydroxide precipitate precipitation solution obtained in Embodiment 3 has a moisture content of 52.8% after being subjected to filter pressing by the filter press.
(18) After detection and calculation, the mixed hydroxide precipitate particles prepared in Embodiment 3 contain 39.6% of nickel and 3.28% of cobalt, with a nickel-cobalt precipitation rate of 89%.
Embodiment 4
(19) A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy includes the following steps: the embodiment is different from Embodiment 1 only in that: reaction temperature in Steps 1-4 is 70 C.
Embodiment 5
(20) A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy includes the following steps: the embodiment is different from Embodiment 2 only in that: reaction temperature in Steps 1-4 is 70 C.
Embodiment 6
(21) A method for continuously preparing mixed hydroxide precipitate from a laterite nickel ore by hydrometallurgy includes the following steps: the embodiment is different from Embodiment 3 only in that: reaction temperature in Steps 1-4 is 70 C.
Comparative Embodiment 1
(22) A method for preparing mixed hydroxide precipitate from a laterite nickel ore solution after removal of iron and aluminum includes the following steps: the comparative embodiment is different from Embodiment 1 only in that: the number of cycles in Step 4 is 0.
(23) After detection, the mixed hydroxide precipitate particles prepared in Comparative embodiment 1 have: D10=3.032 m, D50=10.998 m, and D90-33.216 m.
(24) The final mixed hydroxide precipitate precipitation solution obtained in Comparative embodiment 1 has a moisture content of 66.12% after being subjected to filter pressing by the filter press.
(25) After detection and calculation, the mixed hydroxide precipitate particles prepared in Comparative embodiment 1 contain 34.77% of nickel and 2.7% of cobalt, with a nickel-cobalt precipitation rate of 80%.
Comparative Embodiment 2
(26) A method for preparing mixed hydroxide precipitate from a laterite nickel ore solution after removal of iron and aluminum includes the following steps: the comparative embodiment is different from Embodiment 1 only in that: the reaction time in Steps 1-4 is 2 h.
Comparative Embodiment 3
(27) A method for preparing mixed hydroxide precipitate from a laterite nickel ore solution after removal of iron and aluminum includes the following steps:
(28) The comparative embodiment is different from Embodiment 1 only in that: the reaction time in Steps 1-4 is 4 h.
Comparative Embodiment 4
(29) A method for preparing mixed hydroxide precipitate from a laterite nickel ore solution after removal of iron and aluminum includes the following steps: the comparative embodiment is different from Embodiment 1 only in that: the reaction temperature in Steps 1-4 is 70 C.
Comparative Embodiment 5
(30) A method for preparing mixed hydroxide precipitate from a laterite nickel ore solution after removal of iron and aluminum includes the following steps: the comparative embodiment is different from Embodiment 2 only in that: the reaction temperature in Steps 1-4 is 70 C.
Comparative Embodiment 6
(31) A method for preparing mixed hydroxide precipitate from a laterite nickel ore solution after removal of iron and aluminum includes the following steps: the comparative embodiment is different from Embodiment 3 only in that: the reaction temperature in Steps 1-4 is 70 C.
(32) The comparative statistical table of the performance of the products in Embodiments 1-6 and Comparative Embodiments 1-6 is shown in Table 1.
(33) TABLE-US-00001 TABLE 1 Comparative statistical table of performance Number Moisture Nickel Cobalt Temperature/ Reaction of Particle size content/ content/ content/ Sample C. time/h cycles distribution % % % Embodiment 60 1 15 D10 = 1.962 m, 53.2 39.5 3.3 1 D50 = 6.915 m, D90 = 15.434 m Embodiment 60 2 20 D10 = 2.142 m, 51.8 39.8 3.32 2 D50 = 7.225 m, D90 = 15.736 m Embodiment 60 4 10 D10 = 1.915 m, 52.8 39.6 3.28 3 D50 = 7.153 m, D90 = 15.582 m Embodiment 70 1 15 D10 = 2.253 m, 52.3 39.72 3.31 4 D50 = 7.105 m, D90 = 16.05 m Embodiment 70 2 20 D10 = 2.342 m, 51.2 40.1 3.33 5 D50 = 7.325 m, D90 = 15.936 m Embodiment 70 4 10 D10 = 2.015 m, 52.5 39.7 3.31 6 D50 = 7.031 m, D90 = 15.782 m Comparative 60 1 0 D10 = 3.032 m, 66.12 34.77 2.7 embodiment D50 = 10.998 m, 1 D90 = 33.216 m Comparative 60 2 0 D10 = 2.944 m, 65.34 34.83 2.72 embodiment D50 = 10.644 m, 2 D90 = 31.115 m Comparative 60 4 0 D10 = 2.869 m, 65.2 35.09 2.74 embodiment D50 = 10.501 m, 3 D90 = 29.244 m Comparative 70 1 0 D10 = 2.752 m, 64.18 35.71 2.81 embodiment D50 = 10.094 m, 4 D90 = 28.996 m Comparative 70 2 0 D10 = 2.696 m, 63.63 36.2 2.85 embodiment D50 = 9.767 m, 5 D90 = 27.234 m Comparative 70 4 0 D10 = 2.673 m, 63.2 36.77 2.89 embodiment D50 = 9.464 m, 6 D90 = 26.278 m
(34) By comparing Embodiments 1-6, it can be seen that the crystal nuclei continuously grow after the precipitation reaction repeated several times, and by controlling the number of cycles, mixed hydroxide precipitate particles with narrow particle size distribution, dense particles, and better sedimentation effect are obtained, thereby reducing the moisture content of MHP.
(35) The growth rate, crystal morphology, particle size, and particle size distribution of crystal nuclei are controlled by controlling the quantity of the primary mixed hydroxide precipitate crystal nuclei, the quantity of the precipitants, the growth time of the crystal nuclei, the stirring speed of the reactor, and a feeding manner.
(36) The foregoing descriptions are implementation manners of this disclosure, but are not intended to limit the protection scope of this disclosure. Any changes and modifications made according to the technical idea of this disclosure shall fall within the protection scope of the claims of this disclosure.