CN219897130U - Wet phosphoric acid double-extraction purifying device - Google Patents
Wet phosphoric acid double-extraction purifying device Download PDFInfo
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- CN219897130U CN219897130U CN202321247124.0U CN202321247124U CN219897130U CN 219897130 U CN219897130 U CN 219897130U CN 202321247124 U CN202321247124 U CN 202321247124U CN 219897130 U CN219897130 U CN 219897130U
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title claims abstract description 154
- 238000000605 extraction Methods 0.000 title claims abstract description 120
- 229910000147 aluminium phosphate Inorganic materials 0.000 title claims abstract description 77
- 238000006243 chemical reaction Methods 0.000 claims abstract description 62
- 238000000746 purification Methods 0.000 claims abstract description 54
- 239000002253 acid Substances 0.000 claims abstract description 41
- 238000003860 storage Methods 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000007788 liquid Substances 0.000 claims description 26
- 230000003009 desulfurizing effect Effects 0.000 claims description 15
- 238000004458 analytical method Methods 0.000 claims description 13
- 238000004062 sedimentation Methods 0.000 claims description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 8
- 239000010452 phosphate Substances 0.000 claims description 8
- 239000012535 impurity Substances 0.000 abstract description 8
- 150000001768 cations Chemical class 0.000 abstract description 6
- 238000006477 desulfuration reaction Methods 0.000 abstract description 5
- 230000023556 desulfurization Effects 0.000 abstract description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052751 metal Inorganic materials 0.000 abstract description 4
- 239000002184 metal Substances 0.000 abstract description 4
- 229910052782 aluminium Inorganic materials 0.000 abstract description 3
- 229910052749 magnesium Inorganic materials 0.000 abstract description 3
- 239000011777 magnesium Substances 0.000 abstract description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 2
- 150000001450 anions Chemical class 0.000 abstract description 2
- 239000011737 fluorine Substances 0.000 abstract description 2
- 229910052731 fluorine Inorganic materials 0.000 abstract description 2
- 229910052742 iron Inorganic materials 0.000 abstract description 2
- 239000003337 fertilizer Substances 0.000 description 10
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000002367 phosphate rock Substances 0.000 description 7
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 3
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- -1 iron-magnesium-aluminum Chemical compound 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000000638 solvent extraction Methods 0.000 description 3
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- PYIXRBAUGAEEEW-UHFFFAOYSA-N [3,5-di(propan-2-yl)phenyl] diphenyl phosphate Chemical compound CC(C)C1=CC(C(C)C)=CC(OP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)=C1 PYIXRBAUGAEEEW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000009388 chemical precipitation Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- CKRORYDHXIRZCH-UHFFFAOYSA-N phosphoric acid;dihydrate Chemical compound O.O.OP(O)(O)=O CKRORYDHXIRZCH-UHFFFAOYSA-N 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Abstract
The utility model belongs to a wet-process phosphoric acid double-extraction purification device, wherein an outlet of a crude phosphoric acid storage tank is connected with an inlet of a pre-extraction reaction kettle; the outlet of the pre-extraction reaction kettle is connected with the inlet of the first concentration tank; the outlet of the concentration tank is connected with the inlet of the purification reaction kettle; the outlet of the purification extraction reaction kettle is connected with the inlet of the second stripping kettle; the outlet of the back extraction reaction kettle is connected with the inlet of the second concentration tank; and the outlet of the second concentration tank is connected with the inlet of the purified phosphoric acid storage tank. The double extraction physical removal of impurities is adopted, and the pre-extraction is to remove metal cations such as iron, magnesium, aluminum and the like from wet phosphoric acid by adopting a high-selectivity cation extractant. The intermediate extraction utilizes concentrated phosphoric acid to carry out extraction, fine desulfurization and back extraction by adopting a high-selectivity anion extractant to obtain back extraction acid. After a large amount of metal cations are removed in the pre-extraction process, the viscosity of the acid is reduced, the steam consumption can be saved when the concentration of phosphoric acid is improved, and meanwhile, the removal of fluorine is facilitated due to the improvement of the acid concentration.
Description
Technical Field
The utility model belongs to the technical field of a sulfuric acid method wet-process phosphoric acid double-extraction purification device, and relates to an obtained wet-process phosphoric acid purification device.
Background
At present, the basic reserve of phosphorite in China is 32.4 hundred million tons, and it has been ascertained that phosphorite resources are distributed in 27 provinces (autonomous regions), but the distribution is centralized, and the distribution is mainly in five provinces of Hubei, sichuan, guizhou, yunnan and Hunan, the total reserve of phosphorite resources in five provinces exceeds 80%, but with the consumption of phosphorite resources, most of the phosphorite resources exhibit low grade characteristics, and the utilization of low grade phosphorite resources is greatly dependent on the technical level of wet phosphoric acid. The wet phosphoric acid has the characteristics of low-grade phosphorite utilization and low process energy consumption compared with the hot phosphoric acid, but has the inherent defects of high impurity content of phosphoric acid and high purification difficulty.
With the rise of new energy, the demand for high-purity phosphoric acid is increasing, so that the purification of phosphoric acid is particularly urgent. The phosphoric acid purifying method has a plurality of chemical precipitation, solvent extraction, crystallization, ion exchange and the like, and the solvent extraction is taken as a main flow process route in China at present, wherein the extraction process taking Vat Fu as a main flow process can continuously and industrially produce food grade phosphoric acid, and the Sichuan Dai and Hua Shi solvent extraction purifying processes meet the industrial phosphoric acid requirement.
Analysis of the wet phosphoric acid produced by collophanite in the Hubei area shows that the content of the iron-magnesium-aluminum sesquioxide in the acid is high, the MER value (the ratio of the sum of the percentage contents of the sesquioxide in the phosphoric acid to the percentage content of phosphorus pentoxide) is as high as 8 percent, and when dilute phosphoric acid is concentrated, the iron-magnesium-aluminum ion influence causes high acid viscosity, high energy consumption during concentration, difficult acid concentration and larger influence on the subsequent extraction efficiency improvement. Further, the removal of anions also has a problem of difficult removal.
Disclosure of Invention
In order to solve the problems, the main purpose is to provide a double-extraction suspension crystallization impurity removal technical route aiming at the defects existing in the prior extraction technology. Can effectively remove impurities under the condition of high impurity content of wet-process phosphoric acid to obtain high-purity wet-process purified phosphoric acid. The whole process has high extraction rate and low yield of raffinate acid, and is suitable for a new production device for large-scale production.
The technical scheme of the device comprises the following two procedures in series connection structure, and the device part is as follows: the wet-process phosphoric acid double-extraction purification device is characterized in that an outlet of a crude phosphoric acid storage tank is connected with an inlet of a pre-extraction reaction kettle;
the outlet of the pre-extraction reaction kettle is connected with the inlet of the first concentration tank;
the outlet of the first concentrating tank is connected with the inlet of the purifying extraction reaction kettle;
the outlet of the purification extraction reaction kettle is connected with the inlet of the second stripping kettle;
the outlet of the second stripping kettle is connected with the inlet of the second concentrating tank;
and the outlet of the second concentration tank is connected with the inlet of the purified phosphoric acid storage tank.
The outlet of the crude phosphoric acid storage tank is connected with the inlet of the sedimentation tower, and the outlet of the sedimentation tower is connected with the inlet of the clear liquid tank; the outlet of the clear liquid tank is connected with the inlet of the pre-extraction reaction kettle.
The other outlet of the pre-extraction reaction kettle is connected with the inlet of the first back-extraction kettle.
The outlet of the first stripping kettle is connected with the inlet of the pre-extraction storage tank, and the outlet of the pre-extraction storage tank is connected with the inlet of the pre-extraction reaction kettle; the outlet of the first stripping kettle is connected to a phosphate storage tank.
The outlet of the purification extraction reaction kettle is connected with the inlet of the desulfurizing tower, and the outlet of the desulfurizing tower is connected with the inlet of the back extraction kettle II.
The outlet of the second stripping kettle is connected with the inlet of a stripping acid storage tank;
the outlet of the back extraction acid storage tank is connected with the inlet of the desolventizing reaction kettle;
the outlet of the desolventizing reaction kettle is connected with the inlet of the decoloring reaction kettle;
the outlet of the decoloring reaction kettle is connected with the inlet of the second concentrating tank.
The outlet of the back extraction kettle II is connected with the inlet of the purifying extractant storage tank, and the outlet of the purifying extractant storage tank is connected with the inlet of the purifying extraction reaction kettle.
The outlet of the purifying extraction reaction kettle and the outlet of the desulfurizing tower are respectively connected with the raffinate acid analysis tower.
The outlet of the sedimentation tower and the outlet of the raffinate acid analysis tower are respectively connected with the inlet of the filter.
The outlet of the filter is respectively connected with the inlet of the clear liquid tank and the inlet of the phosphate storage tank.
The process method comprises the following steps:
1. pre-purification procedure:
(1) Step 1, pre-sedimentation: and (3) delivering 30% -50% of the crude phosphoric acid into a settling tank, settling by adding a settling agent to obtain clear acid, overflowing the clear acid into a clear liquid tank, performing solid-liquid separation on the lower silt acid through filter pressing, delivering the solid to a fertilizer workshop to produce fertilizer, and returning clear liquid to the clear liquid tank.
(2) Step 2, pre-extraction: and (3) sending the clear liquid obtained in the step (1) and the pre-extractant into an extraction tower, and carrying out extraction reaction in a countercurrent contact mode to obtain a light phase (1) and a heavy phase (2).
(3) Step 3, desolventizing: and (3) desolventizing the light phase 1 obtained in the step (2) to obtain phosphate, and producing the fertilizer.
(4) Step 4, desolventizing: concentrating the heavy phase obtained in the step 2 to obtain 53-65% concentrated phosphoric acid.
2. Intermediate purification process:
(1) Step 1, extraction: and (3) delivering the 53-65% concentrated phosphoric acid obtained in the step (4) of the pre-purification procedure to a purification tower and purifying an extracting agent for countercurrent extraction reaction to obtain a light phase 2 and a heavy phase 2 containing phosphorus pentoxide.
(2) And 2, fine desulfurization: and (3) carrying out reaction fine desulfurization on the light phase 2 obtained in the step 1 of the intermediate purification process by using a desulfurizing agent, and washing to obtain a light phase 3 and a heavy phase 3. The desulfurizing agent is dilute phosphoric acid solution with barium carbonate.
(3) Step 3, back extraction: and (3) carrying out back extraction on the light phase 2 obtained in the step 2 of the intermediate purification process by using desalted water to obtain a light phase 4 and a heavy phase 4. The light phase 4 returns to the purification and extraction process for cyclic reaction, and the heavy phase 4 is the stripping acid with the concentration of 38-42% obtained after intermediate purification.
(4) And 4, raffinate acid analysis: and (3) the heavy phase 2 obtained in the step (1) in the intermediate purification process is subjected to solvent analysis to obtain raffinate, and the raffinate is filtered to obtain clear liquid, and the clear liquid returns to a clear liquid tank in the pre-purification process to participate in the pre-extraction reaction. And delivering the filtered phosphorus-containing waste residue to a fertilizer process to produce the fertilizer.
(5) Step 5, stripping acid analysis: and (3) carrying out solvent analysis and concentration on the strip acid obtained in the step (3) in the intermediate purification process to obtain the phosphoric acid with 42-45% of concentration without solvent.
(6) And step 6, decoloring: and (3) decoloring the phosphoric acid obtained in the step (5) in the intermediate purification step by using activated carbon to obtain decolored acid.
(7) And 7, concentrating: and (3) carrying out flash evaporation on the decolorized acid obtained in the step (6) in the intermediate purification process to concentrate the acid to concentrated phosphoric acid with the phosphorus pentoxide content of 61-65%.
The utility model has the beneficial effects that
The device of the utility model adopts an extraction mode to remove metal cations in pretreatment, and can be suitable for a high impurity system of raw material acid, in particular to phosphoric acid of a high-aluminum high-magnesium system in a semi-water two-water wet phosphoric acid process.
The post-purification can produce phosphoric acid with different quality according to the process requirement, meanwhile, the low-temperature crystallization process scheme can reduce the dependence on materials, and the requirements can be met by common domestic 316L or 2205.
After a large amount of metal cations are removed in the pre-extraction process, the viscosity of the acid is reduced, the steam consumption can be saved when the concentration of phosphoric acid is improved, and meanwhile, the removal of fluorine is facilitated due to the improvement of the acid concentration.
Drawings
FIG. 1 is a schematic diagram of a wet process phosphoric acid double extraction purification device, wherein 1 a crude phosphoric acid storage tank, 2 a settling tower, 3 a clear liquid tank, 4 a pre-extraction reaction kettle, 5 a strip extraction kettle I, 6 a pre-extraction storage tank, 7 a phosphate storage tank, 8 a concentration tank I, 9 a purification extraction reaction kettle, 10 a desulfurizing tower, 11 a purification extractant storage tank, 12 a strip extraction kettle II, 13 a strip acid storage tank, 14 a desolventizing reaction kettle, 15 a decolorizing reaction kettle, 16 a concentration tank II, 17 a purified phosphoric acid storage tank, 18 a raffinate acid analysis tower and 19 a filter.
Detailed Description
Example 1
For a better understanding of the present utility model, the following examples are set forth to further illustrate the utility model.
The wet-process phosphoric acid double-extraction purification device is characterized in that an outlet of a crude phosphoric acid storage tank 1 is connected with an inlet of a pre-extraction reaction kettle 4;
the outlet of the pre-extraction reaction kettle 4 is connected with the inlet of the first concentration tank 8;
the outlet of the concentration tank 8 is connected with the inlet of the purifying extraction reaction kettle 9;
the outlet of the purification extraction reaction kettle 9 is connected with the inlet of the back extraction kettle II 12;
the outlet of the back extraction reaction kettle 12 is connected with the inlet of a second concentration tank 16;
the outlet of the second concentration tank 16 is connected with the inlet of the purified phosphoric acid storage tank 17.
The outlet of the crude phosphoric acid storage tank 1 is connected with the inlet of the sedimentation tower 2, and the outlet of the sedimentation tower 2 is connected with the inlet of the clear liquid tank 3; the outlet of the clear liquid tank 3 is connected with the inlet of the pre-extraction reaction kettle 4.
The other outlet of the pre-extraction reaction kettle 4 is connected with the inlet of the first stripping kettle 5.
The outlet of the first stripping kettle 5 is connected with the inlet of the pre-extraction storage tank 6, and the outlet of the pre-extraction storage tank 6 is connected with the inlet of the pre-extraction reaction kettle 4; the outlet of the first stripping tank 5 is connected on the other hand to a phosphate storage tank 7.
The outlet of the purification extraction reaction kettle 9 is connected with the inlet of the desulfurizing tower 10, and the outlet of the desulfurizing tower 10 is connected with the inlet of the back extraction kettle II 12.
The outlet of the second stripping kettle 12 is connected with the inlet of a stripping acid storage tank 13;
the outlet of the back extraction acid storage tank 13 is connected with the inlet of the desolventizing reaction kettle 14;
the outlet of the desolventizing reaction kettle 14 is connected with the inlet of the decoloring reaction kettle 15;
the outlet of the decoloring reaction kettle 15 is connected with the inlet of a second concentrating tank 16.
The outlet of the second stripping kettle 12 is connected with the inlet of the purifying extractant storage tank 11, and the outlet of the purifying extractant storage tank 11 is connected with the inlet of the purifying extraction reaction kettle 9.
The outlet of the purifying extraction reaction kettle 9 and the outlet of the desulfurizing tower 10 are respectively connected with a raffinate analyzing tower 21.
The outlet of the sedimentation tower 2 and the outlet of the raffinate acid analysis tower 18 are respectively connected with the inlet of a filter 19. The filter is a plate and frame filter in some embodiments that achieves separation of dilute phosphoric acid from solid impurities.
The outlet of the filter 19 is connected with the inlet of the clear liquid tank 3 and the inlet of the phosphate storage tank 7 respectively.
Example 2
The wet process phosphoric acid dihydrate crude phosphoric acid is used as raw material phosphoric acid, and the index of the crude phosphoric acid is shown in Table 1, but the content of the utility model is not limited to the following examples
TABLE 1 phosphoric acid parameter index
The wet process phosphoric acid purification process is carried out by adopting the process and the crude phosphoric acid with the number of 4, and the specific steps are as follows:
preparation of the pre-extractant: adding tris (2, 4-di-tert-butylphenyl) phosphite ester into n-butanol to prepare a mixed solution with the mass concentration of 15.5wt%, and mixing the mixed solution at a high speed of 600r/min for 10min to obtain an extraction solvent.
Configuration of purifying extractant: 3, 5-bis (isopropyl) phenyl diphenyl phosphate and 2-hexanone in a volume ratio of 1:22, and mixing at a high speed of 700r/min for 10min to form a transparent suspension.
Desulfurizing agent: the mass concentration of the diluted phosphoric acid solution of the calcium bicarbonate is 35%, and the mass fraction of the calcium bicarbonate in the diluted phosphoric acid solution of the calcium bicarbonate is 30%.
1. Pre-purification procedure:
(1) Step 1, pre-sedimentation: and (3) conveying the crude phosphoric acid with the number of 3 into a settling tank, settling for 1h by adding a settling agent (polyacrylamide) to obtain clear acid, overflowing the clear acid into a clear liquid tank, performing filter pressing solid-liquid separation on the lower silt acid, conveying the solid to a fertilizer workshop to produce fertilizer, and returning clear liquid to the clear liquid tank.
(2) Step 2, pre-extraction: the temperature in the extraction tower is 45+/-5 ℃, the pressure in the extraction tower is 0.5-0.6MPa, the clear liquid obtained in the step 1 and the pre-extractant are respectively preheated to 45+/-5 ℃, then respectively enter the extraction tower from the upper part and the lower part of the extraction tower together for countercurrent contact extraction, a turntable tower is adopted for emulsification and dispersion in the extraction process, the volume ratio of wet phosphoric acid to the extraction solvent is 1:2, the contact extraction time is 5min, and the light phase 1 and the heavy phase 1 are collected after the extraction reaction is completed.
(3) Step 3, desolventizing: adding 30% of dilute sulfuric acid with the mass fraction of 30% into the light phase 1 obtained in the step 2 to remove cations such as calcium, magnesium and aluminum, adding 10% of oxalic acid to remove impurity cationic iron to obtain an empty pre-extractant, and adding 10% of fresh pre-extractant into the obtained pre-extractant for continuous pre-extraction; the separated cation salt is used for producing fertilizer additives.
(4) Step 4, desolventizing: concentrating the heavy phase 1 obtained in the step 2 to obtain 52-55% concentrated phosphoric acid.
2. Intermediate purification process:
(1) Step 1, extraction: the temperature in the purifying extraction tower is 45+/-5 ℃, the pressure in the purifying extraction tower is 0.01-0.05MPa, and the 52-55% concentrated phosphoric acid and the purifying extractant obtained in the step 4 of the pre-purifying procedure are respectively preheated to 45+/-5 ℃, and the volume ratio of the 52-55% concentrated phosphoric acid to the purifying extractant is 1:2 respectively enter the extraction tower from the upper part and the lower part of the extraction tower to carry out contact extraction, and the wet phosphoric acid and the extraction solvent are respectively emulsified and dispersed into particles with the granularity of 120 mu m by a turntable tower in the contact extraction process, and the light phase 2 and the heavy phase 2 containing phosphorus pentoxide are collected after 3min of contact reaction.
(2) And 2, fine desulfurization: and (3) carrying out reaction fine desulfurization on the light phase 2 obtained in the step 1 of the intermediate purification process by using a desulfurizing agent, wherein the volume ratio of the light phase 2 to the desulfurizing agent is 10:1, washing to obtain a light phase 3 and a heavy phase 3.
(3) Step 3, back extraction: and (3) carrying out back extraction on the light phase 3 obtained in the step (2) of the intermediate purification process by using desalted water to obtain a light phase 4 and a heavy phase 4. The light phase 4 is supplemented with 5 percent of purifying extractant with volume fraction, the purified extractant returns to the purifying extraction procedure for cyclic reaction, and the heavy phase 4 is stripping acid with mass concentration of 40-42 percent obtained after intermediate purification.
(4) And 4, raffinate acid analysis: and (3) mixing the heavy phase 2 obtained in the step (1) of the intermediate purification process with the heavy phase 3 obtained in the step (2), removing the solvent contained in the mixture by analysis to obtain raffinate, filtering the raffinate to obtain clear liquid, and returning the clear liquid to a clear liquid tank of the pre-purification process to participate in the pre-extraction reaction. And delivering the filtered phosphorus-containing waste residue to a fertilizer process to produce the fertilizer.
(5) Step 5, stripping acid analysis: and (3) carrying out vacuum rectification and desolventizing on the stripping acid with the mass concentration of 40-42% obtained in the step (3) in the intermediate purification process at the absolute pressure of 10-30KPaA and the temperature of 85-100 ℃ to obtain the phosphoric acid with the concentration of 42-50% without solvent.
(6) And step 6, decoloring: and (3) decoloring the phosphoric acid obtained in the step (5) in the intermediate purification step by using activated carbon to obtain decolored acid.
(7) And 7, concentrating: and (3) carrying out vacuum flash evaporation and concentration on the decolorized acid obtained in the step 6 in the intermediate purification process at 90-120 ℃ under the absolute pressure of 10-25KPaA to obtain concentrated phosphoric acid with the phosphorus pentoxide content of 64-65%.
Claims (10)
1. The wet-process phosphoric acid double-extraction purification device is characterized in that an outlet of a crude phosphoric acid storage tank (1) is connected with an inlet of a pre-extraction reaction kettle (4);
the outlet of the pre-extraction reaction kettle (4) is connected with the inlet of the first concentration tank (8);
the outlet of the first concentrating tank (8) is connected with the inlet of the purifying extraction reaction kettle (9);
the outlet of the purification extraction reaction kettle (9) is connected with the inlet of the back extraction kettle II (12);
the outlet of the second stripping kettle (12) is connected with the inlet of the second concentrating tank (16);
the outlet of the second concentrating tank (16) is connected with the inlet of the purified phosphoric acid storage tank (17).
2. The wet-process phosphoric acid double-extraction purification device according to claim 1, wherein the outlet of the crude phosphoric acid storage tank (1) is connected with the inlet of the sedimentation tower (2), and the outlet of the sedimentation tower (2) is connected with the inlet of the clear liquid tank (3); the outlet of the clear liquid tank (3) is connected with the inlet of the pre-extraction reaction kettle (4).
3. The wet-process phosphoric acid double-extraction purification device according to claim 2, wherein the other outlet of the pre-extraction reaction kettle (4) is connected with the inlet of the back-extraction kettle I (5).
4. A wet-process phosphoric acid double-extraction purification device according to claim 3, wherein the outlet of the first stripping kettle (5) is connected with the inlet of a pre-extraction storage tank (6), and the outlet of the pre-extraction storage tank (6) is connected with the inlet of a pre-extraction reaction kettle (4); the outlet of the first stripping kettle (5) is connected to a phosphate storage tank (7) on the other hand.
5. The wet-process phosphoric acid double-extraction purification device according to claim 1, wherein an outlet of the purification extraction reaction kettle (9) is connected with an inlet of a desulfurizing tower (10), and an outlet of the desulfurizing tower (10) is connected with an inlet of a stripping kettle II (12).
6. The wet-process phosphoric acid double-extraction purification device according to claim 5, wherein the outlet of the second stripping kettle (12) is connected with the inlet of a stripping acid storage tank (13);
the outlet of the back extraction acid storage tank (13) is connected with the inlet of the desolventizing reaction kettle (14);
the outlet of the desolventizing reaction kettle (14) is connected with the inlet of the decoloring reaction kettle (15);
the outlet of the decoloring reaction kettle (15) is connected with the inlet of a second concentrating tank (16).
7. The wet-process phosphoric acid double-extraction purification device according to claim 6, wherein the outlet of the second stripping kettle (12) is connected with the inlet of the purifying extractant storage tank (11), and the outlet of the purifying extractant storage tank (11) is connected with the inlet of the purifying extraction reaction kettle (9).
8. The wet-process phosphoric acid double-extraction purification device according to claim 7, wherein the outlet of the purification extraction reaction kettle (9) and the outlet of the desulfurizing tower (10) are respectively connected with a raffinate resolving tower (18).
9. The wet-process phosphoric acid double-extraction purification device according to claim 8, wherein the outlet of the sedimentation tower (2) and the outlet of the raffinate acid analysis tower (18) are respectively connected with the inlet of the filter (19).
10. The wet-process phosphoric acid double-extraction purification device according to claim 9, wherein the outlet of the filter (19) is connected with the inlet of the clear liquid tank (3) and the inlet of the phosphate storage tank (7), respectively.
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