CN218618269U - Storage tank for lithium carbonate impurity removal process - Google Patents

Storage tank for lithium carbonate impurity removal process Download PDF

Info

Publication number
CN218618269U
CN218618269U CN202222575199.3U CN202222575199U CN218618269U CN 218618269 U CN218618269 U CN 218618269U CN 202222575199 U CN202222575199 U CN 202222575199U CN 218618269 U CN218618269 U CN 218618269U
Authority
CN
China
Prior art keywords
tank body
tank
lithium carbonate
storage tank
impurity removal
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.)
Active
Application number
CN202222575199.3U
Other languages
Chinese (zh)
Inventor
刘久传
才利民
陈圆
侯磊
李闯
郜丽慧
郜铁军
张宝森
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.)
Liaoning Hongjing Industry Co ltd
Original Assignee
Liaoning Hongjing 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 Liaoning Hongjing Industry Co ltd filed Critical Liaoning Hongjing Industry Co ltd
Priority to CN202222575199.3U priority Critical patent/CN218618269U/en
Application granted granted Critical
Publication of CN218618269U publication Critical patent/CN218618269U/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Abstract

The utility model relates to a lithium carbonate production technical field, specifically lithium carbonate edulcoration storage tank for technology, including a jar body, the lateral wall lower part of jar body is provided with the discharge gate, and the top surface of jar body is provided with the feed inlet, and the bottom surface of jar body is concave surface, and the low point position in the concave surface is provided with row's cinder notch, and row's cinder notch department installs the sediment control valve; the top surface of the tank body is provided with an air blowing pipeline which is vertically inserted into the tank body, and a nozzle is arranged on a pipe body of the air blowing pipeline positioned in the tank body; an exhaust port is arranged on the top surface of the tank body, and an exhaust valve is arranged at the exhaust port. The storage tank is utilized to realize deep reaction of the impurity removing agent which is not completely reacted in the solution after the primary impurity removal and metal ions, the addition amount of the impurity removing agent is reduced, and the reaction rate is accelerated by a blowing mode and a tank bottom reserved seed crystal mode; in addition, after the deep reaction, the metal ion impurities before the lithium precipitation process can meet the requirements, and EDTA does not need to be added for carrying out the complex reaction.

Description

Storage tank for lithium carbonate impurity removal process
Technical Field
The utility model relates to a lithium carbonate production technical field especially relates to a lithium carbonate storage tank for edulcoration technology.
Background
As a basic raw material for processing and producing lithium battery materials, the battery-grade lithium carbonate has the advantages that the market demand is continuously increased, the quality requirement is continuously improved, and particularly, the impurity requirements on sodium, sulfate radicals, iron, magnesium, aluminum and the like in the product, which have great influence on the chemical performance of the battery, are stricter, so that the impurity removal process becomes an important process for preparing the battery-grade lithium carbonate.
The existing lithium carbonate impurity removal process comprises the following steps: adding the leached and purified lithium sulfate solution into an impurity removal kettle, then adding an impurity removal agent into the impurity removal kettle, specifically adding sodium hydroxide to remove iron ions, aluminum ions and magnesium ions, then adding sodium carbonate to remove calcium ions to complete preliminary impurity removal, filtering the solution subjected to preliminary impurity removal by a precision filter, discharging into a crystallization kettle with a prepared sodium carbonate saturated solution to precipitate lithium, and finally adding EDTA into the crystallization kettle to complex out the remaining metal ions in the solution after the lithium precipitation is completed.
However, the generation of hydroxide and calcium carbonate and the completion of precipitation in the primary impurity removal process take a long time, and the formation of precipitation of trace calcium is difficult under the conditions of no crystal seed intervention and no serious excess of carbonate, so the amount of the added impurity removal agent is far beyond the theoretical requirement; in addition, the higher lithium content in the upper solution in the crystallization kettle after the complexation reaction needs to be recycled in the previous process, but part of the complexation metal ions can be recycled back to the previous process along with the upper solution, the lithium sulfate solution can change color along with the gradual increase of the complex, and the long-term accumulation of the complex can also reduce the impurity removal efficiency.
SUMMERY OF THE UTILITY MODEL
To the problem, the embodiment of the utility model provides a lithium carbonate edulcoration storage tank for technology.
In one aspect of the implementation of the utility model, a storage tank for lithium carbonate impurity removal process is provided, which comprises a tank body, wherein a discharge port is arranged at the lower part of the side wall of the tank body, a feed port is arranged at the top surface of the tank body, the feed port is communicated with the discharge port of the precision filter through a pipeline, the discharge port is communicated with the feed port of a crystallization kettle through a pipeline, the bottom surface of the tank body is a concave surface, a slag discharge port is arranged at the position of a low point in the concave surface, and a slag discharge control valve is arranged at the position of the slag discharge port; the top surface of the tank body is provided with an air blowing pipeline which is vertically inserted into the tank body, and a nozzle is arranged on a pipe body of the air blowing pipeline positioned in the tank body; an exhaust port is arranged on the top surface of the tank body, and an exhaust valve is arranged at the exhaust port.
Compared with the prior art, the beneficial effects of the utility model reside in that: when the storage tank is used for removing impurities, the amount of the required impurity removing agent can be calculated according to the content of impurities in the primary impurity removing process and added into an impurity removing kettle, the solution after primary impurity removal enters the tank body for storage, gas is blown into the solution through a gas blowing pipeline in the storage process to enable the solution to be slowly stirred, the impurity removing agent which is not completely reacted and metal ions in the solution after primary impurity removal are enabled to further perform deep reaction in the storage tank, gas blowing is stopped after the deep reaction is performed for a certain time, precipitate generated by reaction is statically enabled to be precipitated, the precipitate is discharged from a slag discharging port after reaching a certain amount, and a small amount of precipitate is reserved at the bottom of the tank to be used as seed crystal for the next deep reaction to accelerate the reaction rate during slag discharging; after the precipitation is finished, discharging the upper solution into a crystallization kettle through a discharge port to precipitate lithium. The storage tank is used for realizing deep reaction of the impurity removing agent which is not completely reacted in the solution after the primary impurity removal and metal ions, the addition amount of the impurity removing agent is reduced, and the reaction rate is accelerated by a blowing mode and a tank bottom reserved seed crystal mode; and after the deep reaction, the metal ion impurities before the lithium precipitation process can meet the requirements, and EDTA does not need to be added for carrying out the complex reaction.
Optionally, the blowing pipeline is provided with a plurality ofly, and uses the jar body axis as the central line symmetric distribution.
Optionally, a plurality of nozzles are vertically installed on each air blowing pipeline at intervals, and the direction of all the nozzles is the tangential direction of a cylindrical surface which takes the axis of the tank body as a central line.
Optionally, the nozzle is of duckbill type.
Drawings
The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this application, illustrate embodiment(s) of the invention and together with the description serve to explain the principle of the invention. In the drawings:
fig. 1 is a schematic structural diagram of a storage tank for a lithium carbonate impurity removal process provided by an embodiment of the present invention;
fig. 2 is a schematic view of a overlooking structure of a storage tank for a lithium carbonate impurity removal process provided by an embodiment of the utility model.
Wherein, jar body 1, discharge gate 2, feed inlet 3, row's cinder notch 4, gas blowing pipeline 5, nozzle 6, gas vent 7.
Detailed Description
To make the objects, technical solutions and advantages of the present invention more apparent, the present invention will be described in further detail with reference to the following embodiments and accompanying drawings. The exemplary embodiments and descriptions of the present invention are provided to explain the present invention, but not to limit the present invention.
Referring to fig. 1 and 2, the storage tank for the lithium carbonate impurity removal process provided by the embodiment of the invention comprises a tank body 1, wherein a discharge port 2 is arranged at the lower part of the side wall of the tank body 1, a feed port 3 is arranged on the top surface of the tank body 1, the feed port 3 is communicated with the discharge port of the precision filter through a pipeline, the discharge port 2 is communicated with the feed port of the crystallization kettle through a pipeline, the bottom surface of the tank body 1 is a lower concave surface, a slag discharge port 4 is arranged at the lower position in the lower concave surface, and a slag discharge control valve is arranged at the slag discharge port 4; an air blowing pipeline 5 vertically inserted into the tank body 1 is arranged on the top surface of the tank body 1, and a nozzle 6 is arranged on a pipe body of the air blowing pipeline 5 positioned in the tank body 1; an exhaust port 7 is arranged on the top surface of the tank body 1, and an exhaust valve is arranged at the exhaust port.
In implementation, a plurality of air blowing pipelines 5 are arranged and symmetrically distributed by taking the axis of the tank body 1 as a central line; a plurality of nozzles 6 are vertically arranged on each air blowing pipeline 5 at intervals, the orientation of all the nozzles 6 is the tangential direction of a cylindrical surface taking the axis of the tank body 1 as the central line, the nozzles 6 on each air blowing pipeline 5 can be arranged clockwise, and the solution is blown clockwise and stirred towards the same direction; the nozzle 6 is of duckbill type.
The lithium carbonate impurity removal process carried out by the storage tank by applying the scheme comprises the following steps: adding a leached and purified lithium sulfate solution into an impurity removal kettle, adding an impurity removal agent with a corresponding dose according to the content of metal ion impurities in the impurity removal kettle to carry out primary impurity removal, filtering the solution subjected to the primary impurity removal by a precision filter, and then discharging the filtered solution into a storage tank, after the tank body of the storage tank is filled with the solution, blowing gas into the solution in the tank body through a gas blowing pipeline to slowly stir the solution, so that the impurity removal agent which is not completely reacted in the solution subjected to the primary impurity removal and the metal ion impurities are subjected to deep reaction, and the ion reaction rate can be accelerated by utilizing the gas stirring, so that the impurity removal is more thorough; stopping blowing after the deep reaction is carried out for 20 hours, so that precipitates generated by the deep reaction are statically precipitated, and discharging the precipitated upper-layer solution into a crystallization kettle for precipitating lithium through a discharge port after the precipitates are statically precipitated for 4 hours; the sediment at the lower part in the tank body can be used as seed crystals for removing impurities in the next deep reaction, so that the sediment separation is accelerated, the seed crystals are discharged from a slag discharge port after reaching a certain amount, and a small amount of sediment needs to be reserved at the bottom of the tank during slag discharge;
the storage tank is utilized to further carry out deep reaction on the impurity removing agent which is not completely reacted and metal ion impurities in the solution after primary impurity removal, and the precipitate reserved at the bottom of the tank is used as a crystal seed to accelerate the precipitation of the precipitate, so that excessive impurity removing agent is not required to be added into the impurity removing kettle; in addition, the content of metal ions in the solution can meet the requirement through further deep reaction, and the residual metal ions in the solution can be recycled without adding EDTA (ethylene diamine tetraacetic acid) to complex after the lithium precipitation is finished.
The above description is only a preferred embodiment of the present invention, and is not intended to limit the scope of the present invention. Any modification, equivalent replacement, or improvement made within the spirit and principle of the present invention shall fall within the protection scope of the present invention.

Claims (4)

1. A storage tank for a lithium carbonate impurity removal process comprises a tank body, wherein a discharge port is formed in the lower portion of the side wall of the tank body, a feed port is formed in the top surface of the tank body, the feed port is communicated with the discharge port of a precision filter through a pipeline, and the discharge port is communicated with the feed port of a crystallization kettle through a pipeline; the top surface of the tank body is provided with an air blowing pipeline which is vertically inserted into the tank body, and a nozzle is arranged on a pipe body of the air blowing pipeline positioned in the tank body; an exhaust port is arranged on the top surface of the tank body, and an exhaust valve is arranged at the exhaust port.
2. The storage tank for the lithium carbonate impurity removing process according to claim 1, wherein a plurality of the air blowing pipelines are arranged and are symmetrically distributed by taking the axis of the tank body as a central line.
3. The storage tank for the impurity removing process of the lithium carbonate as claimed in claim 2, wherein a plurality of nozzles are vertically installed on each air blowing pipeline at intervals, and all the nozzles are oriented in the tangential direction of a cylindrical surface with the axis of the tank body as the center line.
4. The storage tank for the impurity removing process of lithium carbonate according to any one of claims 1 to 3, wherein the nozzle is of a duckbill type.
CN202222575199.3U 2022-09-28 2022-09-28 Storage tank for lithium carbonate impurity removal process Active CN218618269U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202222575199.3U CN218618269U (en) 2022-09-28 2022-09-28 Storage tank for lithium carbonate impurity removal process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202222575199.3U CN218618269U (en) 2022-09-28 2022-09-28 Storage tank for lithium carbonate impurity removal process

Publications (1)

Publication Number Publication Date
CN218618269U true CN218618269U (en) 2023-03-14

Family

ID=85468813

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202222575199.3U Active CN218618269U (en) 2022-09-28 2022-09-28 Storage tank for lithium carbonate impurity removal process

Country Status (1)

Country Link
CN (1) CN218618269U (en)

Similar Documents

Publication Publication Date Title
CN102020295B (en) Preparation method of high-purity lithium carbonate
CN109775732A (en) Adjust the preparation method of the high-purity lithium carbonate of granularity, size distribution and shape
CN110808369B (en) Preparation method of low-sodium-sulfur nickel-cobalt-aluminum ternary precursor
CN113620355B (en) Preparation method and preparation device of battery anode material powder
CN108642310A (en) A method of complex-precipitation removes aluminium from rare earth feed liquid
CN114655969B (en) Method for preparing lithium carbonate and iron phosphate by recycling high-impurity lithium iron phosphate positive electrode waste material
CN107459069A (en) A kind of method for reducing nickel cobalt aluminium presoma sulfur content
CN115043383A (en) High-tap-density battery-grade iron phosphate and preparation method thereof
CN114854987B (en) Nickel-cobalt precipitation method for removing iron-aluminum solution by acid leaching of laterite-nickel ore
CN207856912U (en) A kind of lithium battery tertiary precursor synthesis apparatus system
CN113149091A (en) Battery-grade nickel salt and preparation method thereof
CN106745102A (en) A kind of preparation technology of lithium carbonate
CN109354077A (en) A kind of ternary precursor and preparation method thereof of polycrystalline form
CN218618269U (en) Storage tank for lithium carbonate impurity removal process
CN1086361C (en) Production technology of yellow flaky sodium sulfide with low carbon and iron contents
WO2024066175A1 (en) Method for removing carbonate radicals from lithium precipitation mother liquor
CN110512075B (en) Method for deeply purifying and removing cadmium from cobalt-manganese sulfate mixed liquid
CN211521610U (en) Purification and drying treatment device for ammonium sulfate solution as byproduct in desulfurization by lead plaster ammonium method
CN112919506B (en) Device and method for continuously producing lithium chloride from salt lake lithium-rich brine
CN210163330U (en) Waste acid recycling production system for etching process
CN113845156A (en) Preparation method of low-sodium-sulfur ultrahigh-nickel quaternary precursor
AU2014314824B2 (en) Nickel hydroxide product and preparation method thereof
CN113061750A (en) Method for extracting and recovering lithium from lithium salt solution and reaction system thereof
CN217868144U (en) Iron phosphate synthesis system
CN115072751B (en) Method for preparing low-fluorine lithium carbonate by recycling lithium iron phosphate battery

Legal Events

Date Code Title Description
GR01 Patent grant
GR01 Patent grant