CN112897544A - Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake - Google Patents

Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake Download PDF

Info

Publication number
CN112897544A
CN112897544A CN202110124045.XA CN202110124045A CN112897544A CN 112897544 A CN112897544 A CN 112897544A CN 202110124045 A CN202110124045 A CN 202110124045A CN 112897544 A CN112897544 A CN 112897544A
Authority
CN
China
Prior art keywords
boron
brine
lithium
borax
purity
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN202110124045.XA
Other languages
Chinese (zh)
Other versions
CN112897544B (en
Inventor
朱红卫
马存彪
王守恒
张青山
张学鹏
吕春英
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Golmud Cangge Lithium Industry Co ltd
Original Assignee
Golmud Cangge Lithium Industry Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Golmud Cangge Lithium Industry Co ltd filed Critical Golmud Cangge Lithium Industry Co ltd
Priority to CN202110124045.XA priority Critical patent/CN112897544B/en
Publication of CN112897544A publication Critical patent/CN112897544A/en
Application granted granted Critical
Publication of CN112897544B publication Critical patent/CN112897544B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B35/00Boron; Compounds thereof
    • C01B35/08Compounds containing boron and nitrogen, phosphorus, oxygen, sulfur, selenium or tellurium
    • C01B35/10Compounds containing boron and oxygen
    • C01B35/12Borates
    • C01B35/121Borates of alkali metal
    • C01B35/122Sodium tetraborates; Hydrates thereof, e.g. borax
    • C01B35/124Preparation by working up natural brines, e.g. seawater
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F9/00Multistage treatment of water, waste water or sewage
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/80Compositional purity
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/42Treatment of water, waste water, or sewage by ion-exchange
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/44Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
    • C02F1/441Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis by reverse osmosis
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/44Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
    • C02F1/442Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis by nanofiltration
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/44Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
    • C02F1/444Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis by ultrafiltration or microfiltration
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/66Treatment of water, waste water, or sewage by neutralisation; pH adjustment
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/42Treatment of water, waste water, or sewage by ion-exchange
    • C02F2001/425Treatment of water, waste water, or sewage by ion-exchange using cation exchangers
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2209/00Controlling or monitoring parameters in water treatment
    • C02F2209/03Pressure

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The invention provides a method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in a salt lake, which comprises the following steps: s1: filtering by a primary nanofiltration system; s2: MVR evaporation concentration; s3: filtering by a secondary nanofiltration system; s4: filtering by a reverse osmosis membrane system; s5: MVR evaporation concentration; s6: adding sulfuric acid and sodium carbonate; s7: filtering by a three-stage nanofiltration system; s8: drying and packaging; step S1 is preceded by the following steps: sending the boron-containing brine into ion exchange resin for treatment to obtain brine containing lithium elements and boron elements; the following steps are also included between step S2 and step S3: and (4) separating the concentrated solution obtained in the step (S2) by using a nanofiltration membrane coated with boron on the surface. According to the invention, after lithium in the boron-containing brine is separated, the boron-containing brine is filtered by the secondary nanofiltration system, the reverse osmosis membrane system, the MVR evaporation and concentration, the sulfuric acid and the sodium carbonate are added, and the tertiary nanofiltration system is used for filtering, so that high-purity borax can be produced, a large amount of fresh water can be recovered, and the utilization rate of salt lake resources is improved.

Description

Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake
Technical Field
The invention discloses a method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in a salt lake, and belongs to the technical field of development and comprehensive utilization of salt lake brine resources.
Background
Boron is an element which is widely distributed and is one of the most important elements in the earth crust, China is one of the countries with rich boron resources in the world, B2O3The geological reserve is in the fifth place of the world. In recent years, with rapid development of economy, demand for boron products in various fields is increasing, and development and utilization of boron resources are greatly advanced. The product containing boron is widely applied to the fields of chemical industry, metallurgy, military industry, machinery, medicine and the like, and borax (Na)2B4O7·10H2O) is increasingly taking an important position in all industries.
The boron ion content in the Carlo salt lake brine is about 30-300ppm, and the development difficulty is large due to too low concentration, so that the development and utilization of boron resources in the Carlo salt lake region are not realized. With the gradual maturity of the process for developing and utilizing the salt lake resources, the separation technology for each ion in the old brine is gradually improved, the ions such as lithium, boron and the like can be extracted from the old brine, the separation is realized by adopting the nanofiltration membrane separation technology, and the salt lake resources are further developed and utilized.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide a method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in a salt lake, so as to solve the problems in the background technology.
In order to achieve the aim, the invention provides a method for producing high-purity borax from boron-containing wastewater of a salt lake, which comprises the following steps: s1: filtering by a primary nanofiltration system; s2: MVR evaporation concentration; s3: filtering by a secondary nanofiltration system; s4: filtering by a reverse osmosis membrane system; s5: MVR evaporation concentration; s6: adding sulfuric acid and sodium carbonate; s7: filtering by a three-stage nanofiltration system; s8: drying and packaging; step S1 is preceded by the following steps: sending the boron-containing brine into ion exchange resin for treatment to obtain brine containing lithium elements and boron elements;
the following steps are also included between step S2 and step S3: and (4) separating the concentrated solution obtained in the step (S2) by using a nanofiltration membrane coated with boron on the surface.
By adopting the scheme, the boron concentration in the boron-containing brine to be treated is lower, the effect is not good by directly utilizing the primary nanofiltration system for filtering, the boron-containing brine is treated by ion exchange resin, can separate lithium element and boron element from low-concentration boron-containing brine to obtain high-concentration boron-containing brine, then a primary nanofiltration system is used for filtration, the primary separation of boron and lithium is realized, the separation effect of boron and lithium is further improved through MVR evaporation concentration and nanofiltration membrane treatment with boron coated on the surface, partial impurity ions are removed through secondary nanofiltration system filtration, reverse osmosis membrane system filtration and MVR evaporation concentration, thereby being beneficial to the subsequent production of high-purity borax, recycling the fresh water generated in the processes of filtering of the secondary nanofiltration system, filtering of the reverse osmosis membrane system and MVR evaporation concentration, and improving the utilization rate of salt lake resources.
Preferably, step S1 specifically includes: heating the lithium-element-containing brine separated from the ion exchange resin to 50-70 ℃, and then sending the lithium-element-containing brine into a primary nanofiltration system for filtering to obtain boron-rich lithium-poor brine A and boron-poor lithium-rich brine B.
By adopting the scheme, the filtering efficiency can be improved.
Preferably, in step S1, the pressure difference between the two sides of the nanofiltration membrane in the primary nanofiltration system is 50-200 bar.
Preferably, step S2 specifically includes: and carrying out MVR evaporation concentration on the boron-poor lithium-rich brine B to obtain a concentrated solution.
Preferably, the concentrated solution obtained in step S2 is filtered by a nanofiltration membrane coated with boron on the surface to obtain boron-rich lithium-poor brine C and boron-poor lithium-rich brine D.
By adopting the scheme, after the surface of the nanofiltration membrane is coated with boron, lithium and boron can be effectively separated, the subsequent recovery of the boron is facilitated, and the lithium carbonate can be produced by adding sodium carbonate into the boron-poor and lithium-rich brine D.
Preferably, step S3 specifically includes: and (4) feeding the boron-rich lithium-poor brine C and the boron-rich lithium-poor brine A obtained in the step (S1) into a secondary nanofiltration system for filtration to obtain boron-rich brine D and fresh water, wherein the pressure difference between two sides of a nanofiltration membrane in the secondary nanofiltration system is 50-200 bar.
Preferably, step S4 specifically includes: and (4) sending the boron-rich brine D obtained in the step (S3) into a reverse osmosis membrane system, applying pressure on two sides of a reverse osmosis membrane, and obtaining the boron-rich brine E and fresh water, wherein the pressure difference is 50-100 bar.
Preferably, step S5 specifically includes: and (4) carrying out MVR evaporation concentration on the boron-rich brine E obtained in the step (S4) to obtain boron-rich brine F and fresh water.
Preferably, step S6 specifically includes: adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 4-6.5, heating to 80-120 ℃, adding sodium carbonate, adjusting the pH of the solution to 8-10, and reacting for 0.5-6h to obtain a borax solution.
By adopting the scheme, the boron-rich brine F is added with sulfuric acid to adjust the pH value of the solution, then sodium carbonate is added, and the purity of the borax produced after separation by the three-stage nanofiltration system is higher.
Preferably, in step S7, the pressure difference between the two sides of the nanofiltration membrane in the three-stage nanofiltration system is 50-200 bar.
Compared with the prior art, the invention has the following beneficial effects:
(1) the boron-containing brine is sent into the ion exchange resin for treatment before the filtration of the primary nanofiltration system, lithium and boron can be separated from the low-concentration boron-containing brine to obtain the high-concentration boron-containing brine, and then the primary nanofiltration system is used for filtration, so that the primary separation of the boron and the lithium is realized, and the recovery rate of the boron and the purity of the recovered borax are improved.
(2) And a nanofiltration membrane with the surface coated with boron is used between the MVR evaporation concentration step and the secondary nanofiltration system filtration step to separate concentrated solution obtained by MVR evaporation concentration, so that the separation effect of boron and lithium is further improved, and the recovery rate of boron and the purity of recovered borax are further improved.
(3) After the lithium element in the boron-containing brine is separated, the boron-containing brine is filtered by a secondary nanofiltration system, a reverse osmosis membrane system, MVR evaporation concentration, sulfuric acid, sodium carbonate and a tertiary nanofiltration system in sequence, so that high-purity borax can be produced, a large amount of fresh water can be recovered, and the utilization rate of salt lake resources is improved.
Drawings
FIG. 1 is a process flow for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in a salt lake.
Detailed Description
In order to make the technical means, the creation characteristics, the achievement purposes and the effects of the invention easy to understand, the invention is further described with the specific embodiments.
Example 1
The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake comprises the following steps:
sending the boron-containing brine into ion exchange resin for treatment to obtain brine containing lithium elements and boron elements;
s1: the first-stage nanofiltration system filters
Heating the lithium element-containing brine obtained by separating the ion exchange resin to 50 ℃, and then sending the lithium element-containing brine into a primary nanofiltration system for filtering to obtain boron-rich lithium-poor brine A and boron-poor lithium-rich brine B, wherein the pressure difference between two sides of a nanofiltration membrane in the primary nanofiltration system is 50 bar;
s2: MVR evaporative concentration
Carrying out MVR evaporation concentration on the boron-poor lithium-rich brine B to obtain a concentrated solution;
filtering the concentrated solution by a nanofiltration membrane with the surface coated with boron to obtain boron-rich lithium-poor brine C and boron-poor lithium-rich brine D;
s3: the second stage nanofiltration system filters
Feeding the boron-rich lithium-poor brine C and the boron-rich lithium-poor brine A obtained in the step S1 into a secondary nanofiltration system for filtration to obtain boron-rich brine D and fresh water, wherein the pressure difference between two sides of a nanofiltration membrane in the secondary nanofiltration system is 50 bar;
s4: reverse osmosis membrane system filtration
Feeding the boron-rich brine D obtained in the step S3 into a reverse osmosis membrane system, applying pressure on two sides of a reverse osmosis membrane, and obtaining boron-rich brine E and fresh water, wherein the pressure difference is 50 bar;
s5: MVR evaporative concentration
Carrying out MVR evaporation concentration on the boron-rich brine E obtained in the step S4 to obtain boron-rich brine F and fresh water;
s6: adding sulfuric acid and sodium carbonate
Adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 4, heating to 80 ℃, adding sodium carbonate, adjusting the pH of the solution to 8, and fully reacting for 0.5h to obtain a borax solution;
s7: filtering of three-stage nanofiltration system
The pressure difference between two sides of the nanofiltration membrane in the three-stage nanofiltration system is 50 bar;
s8: and (6) drying and packaging.
Example 2
The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake comprises the following steps:
in step S1, the temperature of the brine fed into the primary nanofiltration system is 70 ℃, and the pressure difference between two sides of the nanofiltration membrane in the primary nanofiltration system is 200 bar;
in step S3, the pressure difference between the two sides of the nanofiltration membrane in the secondary nanofiltration system is 200 bar;
in step S4, the pressure difference across the reverse osmosis membrane is 100 bar;
in step S6, adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 6.5, heating to 120 ℃, adding sodium carbonate, adjusting the pH of the solution to 10, and reacting for 6 hours to obtain a borax solution;
in step S7, the pressure difference between the two sides of the nanofiltration membrane in the three-stage nanofiltration system is 200 bar;
except for the above experimental parameters, other experimental parameters and experimental procedures were the same as in example 1.
Example 3
The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake comprises the following steps:
in step S1, the temperature of the brine fed into the primary nanofiltration system is 55 ℃, and the pressure difference between two sides of the nanofiltration membrane in the primary nanofiltration system is 80 bar;
in step S3, the pressure difference between the two sides of the nanofiltration membrane in the secondary nanofiltration system is 80 bar;
in step S4, the differential pressure across the reverse osmosis membrane is 60 bar;
in step S6, adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 4.5, heating to 90 ℃, adding sodium carbonate, adjusting the pH of the solution to 9, and reacting for 2 hours to obtain a borax solution;
in step S7, the pressure difference between the two sides of the nanofiltration membrane in the three-stage nanofiltration system is 80 bar;
except for the above experimental parameters, other experimental parameters and experimental procedures were the same as in example 1.
Example 4
The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake comprises the following steps:
in step S1, the temperature of the brine fed into the primary nanofiltration system is 65 ℃, and the pressure difference between two sides of the nanofiltration membrane in the primary nanofiltration system is 120 bar;
in step S3, the pressure difference between the two sides of the nanofiltration membrane in the secondary nanofiltration system is 120 bar;
in step S4, the differential pressure across the reverse osmosis membrane is 80 bar;
in the step S6, adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 6, heating to 110 ℃, adding sodium carbonate, adjusting the pH of the solution to 9, and reacting for 4 hours to obtain a borax solution;
in step S7, the pressure difference between the two sides of the nanofiltration membrane in the three-stage nanofiltration system is 120 bar;
except for the above experimental parameters, other experimental parameters and experimental procedures were the same as in example 1.
Example 5
The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake comprises the following steps:
in step S1, the temperature of the brine fed into the primary nanofiltration system is 70 ℃, and the pressure difference between two sides of the nanofiltration membrane in the primary nanofiltration system is 160 bar;
in step S3, the pressure difference between the two sides of the nanofiltration membrane in the secondary nanofiltration system is 160 bar;
in step S4, the differential pressure across the reverse osmosis membrane is 50 bar;
in step S6, adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 6.5, heating to 80 ℃, adding sodium carbonate, adjusting the pH of the solution to 9, and reacting for 4 hours to obtain a borax solution;
in step S7, the pressure difference between the two sides of the nanofiltration membrane in the three-stage nanofiltration system is 160 bar;
except for the above experimental parameters, other experimental parameters and experimental procedures were the same as in example 1.
Test example 1 Effect of different test parameters on test results
Comparative examples 1 to 5: in the comparative experiments corresponding to examples 1 to 5, the experimental steps were identical to those of the corresponding examples except that the concentrated solution obtained in step S2 was separated between step S2 and step S3 without using a nanofiltration membrane coated with boron on the surface, and the specific experimental results are detailed in table 1.
Comparative examples 6 to 10: comparative experiments corresponding to examples 1-5 were carried out in exactly the same manner as the corresponding examples except that the boron-containing brine was not treated with ion exchange resin prior to step S1, and the results are detailed in table 1.
TABLE 1 recovery of boron and composition of recovered borax
Figure RE-GDA0003005189520000061
Figure RE-GDA0003005189520000071
As can be seen from table 1, the recovery rate of boron element in examples 1 to 5 is greater than 80%, and the purity of the recovered borax is higher than 95%, which indicates that the present invention can effectively recover boron element in boron-containing brine, and the purity of the recovered borax is higher, compared with examples 1 to 5, the recovery rate of boron element in comparative examples 1 to 5 is between 70% and 74%, and the purity of the recovered borax is between 87% and 90%, which indicates that the concentrated solution obtained in step S2 is separated by using a nanofiltration membrane with a boron coated surface between step S2 and step S3, and the recovery rate of boron element and the purity of the recovered borax can be improved.
The recovery rate of the boron element in the comparative examples 6 to 10 is between 52 percent and 54 percent, the purity of the recovered borax is between 60 percent and 62 percent, and the recovery rate of the boron element and the purity of the recovered borax in the comparative examples 6 to 10 are far lower than those in the examples 1 to 5, which shows that the boron-containing brine is sent into ion exchange resin for treatment before the step S1, and the recovery rate of the boron element and the purity of the recovered borax can be obviously improved.
While there have been shown and described what are at present considered the fundamental principles and essential features of the invention and its advantages, it will be apparent to those skilled in the art that the invention is not limited to the details of the foregoing exemplary embodiments, but is capable of other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
Furthermore, it should be understood that although the present description refers to embodiments, not every embodiment may contain only a single embodiment, and such description is for clarity only, and those skilled in the art should integrate the description, and the embodiments may be combined as appropriate to form other embodiments understood by those skilled in the art.

Claims (10)

1. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake comprises the following steps: s1: filtering by a primary nanofiltration system; s2: MVR evaporation concentration; s3: filtering by a secondary nanofiltration system; s4: filtering by a reverse osmosis membrane system; s5: MVR evaporation concentration; s6: adding sulfuric acid and sodium carbonate; s7: filtering by a three-stage nanofiltration system; s8: drying and packaging; the method is characterized by further comprising the following steps before the step S1: sending the boron-containing brine into ion exchange resin for treatment to obtain brine containing lithium elements and boron elements;
the following steps are also included between step S2 and step S3: and (4) separating the concentrated solution obtained in the step (S2) by using a nanofiltration membrane coated with boron on the surface.
2. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 1, wherein the step S1 is specifically as follows: heating the lithium-element-containing brine separated from the ion exchange resin to 50-70 ℃, and then sending the lithium-element-containing brine into a primary nanofiltration system for filtering to obtain boron-rich lithium-poor brine A and boron-poor lithium-rich brine B.
3. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 2, wherein in step S1, the pressure difference between two sides of the nanofiltration membrane in the primary nanofiltration system is 50-200 bar.
4. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 2, wherein the step S2 is specifically as follows: and carrying out MVR evaporation concentration on the boron-poor lithium-rich brine B to obtain a concentrated solution.
5. The method for producing high-purity borax by using boron-containing wastewater discharged in the production of salt lake lithium carbonate according to claim 4, wherein the concentrated solution obtained in the step S2 is filtered by a nanofiltration membrane with a boron-coated surface to obtain boron-rich lithium-poor brine C and boron-poor lithium-rich brine D.
6. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 5, wherein the step S3 is specifically as follows: and (4) feeding the boron-rich lithium-poor brine C and the boron-rich lithium-poor brine A obtained in the step (S1) into a secondary nanofiltration system for filtration to obtain boron-rich brine D and fresh water, wherein the pressure difference between two sides of a nanofiltration membrane in the secondary nanofiltration system is 50-200 bar.
7. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 6, wherein the step S4 is specifically as follows: and (4) sending the boron-rich brine D obtained in the step (S3) into a reverse osmosis membrane system, applying pressure on two sides of a reverse osmosis membrane, and obtaining the boron-rich brine E and fresh water, wherein the pressure difference is 50-100 bar.
8. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 7, wherein the step S5 is specifically as follows: and (4) carrying out MVR evaporation concentration on the boron-rich brine E obtained in the step (S4) to obtain boron-rich brine F and fresh water.
9. The method for producing high-purity borax from boron-containing wastewater discharged in the production of lithium carbonate in salt lake according to claim 8, wherein the step S6 is specifically as follows: adding sulfuric acid into the boron-rich brine F, adjusting the pH of the solution to 4-6.5, heating to 80-120 ℃, adding sodium carbonate, adjusting the pH of the solution to 8-10, and reacting for 0.5-6h to obtain a borax solution.
10. The method for producing high-purity borax from boron-containing wastewater discharged from the production of salt lake lithium carbonate as claimed in claim 1, wherein in step S7, the pressure difference between two sides of the nanofiltration membrane in the three-stage nanofiltration system is 50-200 bar.
CN202110124045.XA 2021-01-29 2021-01-29 Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake Active CN112897544B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110124045.XA CN112897544B (en) 2021-01-29 2021-01-29 Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110124045.XA CN112897544B (en) 2021-01-29 2021-01-29 Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake

Publications (2)

Publication Number Publication Date
CN112897544A true CN112897544A (en) 2021-06-04
CN112897544B CN112897544B (en) 2022-07-12

Family

ID=76120738

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110124045.XA Active CN112897544B (en) 2021-01-29 2021-01-29 Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake

Country Status (1)

Country Link
CN (1) CN112897544B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114917600A (en) * 2022-06-01 2022-08-19 启东神农机械有限公司 Evaporative crystallization process and device for producing borax from salt lake lithium extraction discharge liquid
CN116177557A (en) * 2023-01-13 2023-05-30 格尔木藏格锂业有限公司 Method for preparing borax from wastewater containing boron discharged from electrodialysis process section

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1542147A (en) * 2003-04-30 2004-11-03 中国科学院青海盐湖研究所 Nano-filtration method for separating magnesium and enriching lithium from salt lake brine
US20060249390A1 (en) * 2003-06-23 2006-11-09 Jinying Yan Boron separation and recovery
JP2007301456A (en) * 2006-05-10 2007-11-22 Nec Facilities Ltd Treatment method and treatment apparatus of boron containing waste water
CN103894140A (en) * 2014-03-10 2014-07-02 中国科学院青海盐湖研究所 Boron-strontium ion adsorbent, preparation method and application of adsorbent
US20160013476A1 (en) * 2013-10-29 2016-01-14 Lg Chem, Ltd. Manufacturing method of cathode active material, and cathode active material for lithium secondary battery manufactured thereby
CN105540619A (en) * 2015-08-17 2016-05-04 马培华 Method for directly preparing battery grade lithium carbonate from salt lake brine with high magnesium-to-lithium ratio
CN106629786A (en) * 2016-12-08 2017-05-10 华东理工大学 High selectivity method of extracting lithium from salt lake brine
CN108342595A (en) * 2018-01-26 2018-07-31 天津科技大学 A kind of boron lithium coextraction method in brine
CN108658101A (en) * 2017-08-10 2018-10-16 青海盐湖工业股份有限公司 A kind of new process of salt lake bittern production high-purity lithium chloride
CN109354043A (en) * 2018-11-14 2019-02-19 格尔木藏格锂业有限公司 Clean the method for mentioning lithium from super low concentration brine containing lithium

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1542147A (en) * 2003-04-30 2004-11-03 中国科学院青海盐湖研究所 Nano-filtration method for separating magnesium and enriching lithium from salt lake brine
US20060249390A1 (en) * 2003-06-23 2006-11-09 Jinying Yan Boron separation and recovery
JP2007301456A (en) * 2006-05-10 2007-11-22 Nec Facilities Ltd Treatment method and treatment apparatus of boron containing waste water
US20160013476A1 (en) * 2013-10-29 2016-01-14 Lg Chem, Ltd. Manufacturing method of cathode active material, and cathode active material for lithium secondary battery manufactured thereby
CN103894140A (en) * 2014-03-10 2014-07-02 中国科学院青海盐湖研究所 Boron-strontium ion adsorbent, preparation method and application of adsorbent
CN105540619A (en) * 2015-08-17 2016-05-04 马培华 Method for directly preparing battery grade lithium carbonate from salt lake brine with high magnesium-to-lithium ratio
CN106629786A (en) * 2016-12-08 2017-05-10 华东理工大学 High selectivity method of extracting lithium from salt lake brine
CN108658101A (en) * 2017-08-10 2018-10-16 青海盐湖工业股份有限公司 A kind of new process of salt lake bittern production high-purity lithium chloride
CN108342595A (en) * 2018-01-26 2018-07-31 天津科技大学 A kind of boron lithium coextraction method in brine
CN109354043A (en) * 2018-11-14 2019-02-19 格尔木藏格锂业有限公司 Clean the method for mentioning lithium from super low concentration brine containing lithium

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
YAN CHUNYAN;ET AL.: "Removal of boron from refined brine by using selective ion exchange resins", 《JOURNAL OF HAZARDOUS MATERIALS》 *
肖湘: "离子交换法从盐湖卤水中分离富集硼的工艺及应用基础研究", 《中国博士学位论文全文数据库 工程科技I辑》 *
苏慧等: "从盐湖卤水中提取与回收锂的技术进展及展望", 《材料导报》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114917600A (en) * 2022-06-01 2022-08-19 启东神农机械有限公司 Evaporative crystallization process and device for producing borax from salt lake lithium extraction discharge liquid
CN116177557A (en) * 2023-01-13 2023-05-30 格尔木藏格锂业有限公司 Method for preparing borax from wastewater containing boron discharged from electrodialysis process section

Also Published As

Publication number Publication date
CN112897544B (en) 2022-07-12

Similar Documents

Publication Publication Date Title
WO2017005113A1 (en) Method for extracting lithium from salt lake brine
CN112897544B (en) Method for producing high-purity borax from boron-containing wastewater discharged in production of lithium carbonate in salt lake
CN114212807A (en) Preparation method of lithium hydroxide and lithium carbonate
CN101491323B (en) New production technique of sodium glutamate
CN106946275A (en) The method for directly producing battery-stage monohydrate lithium hydroxide using the rich lithium bittern in salt lake
CN109250856A (en) It is a kind of low cost ferric phosphate nitrogen-containing wastewater processing and recovery method as resource
CN105540619A (en) Method for directly preparing battery grade lithium carbonate from salt lake brine with high magnesium-to-lithium ratio
CN109607578B (en) Method for extracting battery-grade lithium carbonate from magnesium sulfate subtype salt lake brine
CN106882816A (en) A kind of method of concentration and separation boron in salt lake bittern containing lithium
CN105036159A (en) Method for preparing lithium carbonate with high-lithium salt lake bittern
CN113443639B (en) Preparation process of electronic grade potassium hydroxide
CN110436679B (en) Device and method for recycling and comprehensively utilizing washing water of lithium carbonate
CN109534369B (en) Membrane integrated lithium chloride preparation equipment and method thereof
US20240116002A1 (en) Systems and methods for direct lithium hydroxide production
CN108428893B (en) Preparation method of brine lithium carbonate
CN116239132A (en) Method for recovering carbonate in process of preparing battery-grade lithium carbonate from salt lake brine
CN115676856A (en) Method and system for extracting lithium from salt lake
CN110606499A (en) Lithium-containing salt lake brine lithium extraction combined device
CN211111482U (en) Lithium carbonate washing water resource comprehensive utilization's device
CN114014341A (en) Device and method for preparing high-lithium solution from raw halogen
CN106587112A (en) Comprehensive utilization method for brine
CN112661335A (en) Resource utilization method and device for ammonium fluoride waste brine
CN114906828B (en) Method for treating lithium dihydrogen phosphate mother solution
CN105585033B (en) The removal technique of sulfate ion in a kind of potassium chloride brine
CN220056562U (en) Membrane equipment for preparing battery-level lithium hydroxide

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant