[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN106422994B - Method and equipment for preparing ammonium bicarbonate type extraction liquid - Google Patents

Method and equipment for preparing ammonium bicarbonate type extraction liquid Download PDF

Info

Publication number
CN106422994B
CN106422994B CN201610922145.6A CN201610922145A CN106422994B CN 106422994 B CN106422994 B CN 106422994B CN 201610922145 A CN201610922145 A CN 201610922145A CN 106422994 B CN106422994 B CN 106422994B
Authority
CN
China
Prior art keywords
reaction
ejector
absorption coil
heat exchanger
absorption
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
CN201610922145.6A
Other languages
Chinese (zh)
Other versions
CN106422994A (en
Inventor
李桢
刘玲玲
王大新
张承慈
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.)
Beijing Woteer Water Technology Co ltd
Original Assignee
Beijing Woteer Water Technology 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 Beijing Woteer Water Technology Co ltd filed Critical Beijing Woteer Water Technology Co ltd
Priority to CN201610922145.6A priority Critical patent/CN106422994B/en
Publication of CN106422994A publication Critical patent/CN106422994A/en
Application granted granted Critical
Publication of CN106422994B publication Critical patent/CN106422994B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J10/00Chemical processes in general for reacting liquid with gaseous media other than in the presence of solid particles, or apparatus specially adapted therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J4/00Feed or outlet devices; Feed or outlet control devices
    • B01J4/001Feed or outlet devices as such, e.g. feeding tubes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J4/00Feed or outlet devices; Feed or outlet control devices
    • B01J4/008Feed or outlet control devices
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01CAMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C1/00Ammonia; Compounds thereof
    • C01C1/26Carbonates or bicarbonates of ammonium
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01CAMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C1/00Ammonia; Compounds thereof
    • C01C1/28Methods of preparing ammonium salts in general
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A20/00Water conservation; Efficient water supply; Efficient water use
    • Y02A20/124Water desalination
    • Y02A20/131Reverse-osmosis

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Gas Separation By Absorption (AREA)

Abstract

The invention relates to a method and equipment for preparing a carbon ammonium extraction liquid. The equipment comprises a reaction tank, a circulating pump and CO 2 The device comprises a gas storage tank, an ejector, an absorption coil and a finished product storage tank; the outlet and the inlet of the reaction box are respectively communicated with two ends of a pipeline to form an external circulation loop, and the pipeline is sequentially provided with a circulation pump, an ejector and an absorption coil pipe from the outlet to the inlet; the inlet of the ejector is also connected with CO 2 The gas storage tank is communicated; the outlet of the reaction box is also communicated with the finished product storage box. Ammonia water or ammonia water solution is conveyed into the ejector through the circulating pump from the reaction box and is mixed with the CO 2 CO provided in a gas storage tank 2 After being mixed by the ejector, the mixture is further absorbed and reacted in the absorption coil pipe, then the mixture returns to the reaction box and is circulated, and after the reaction in the reaction box obtains carbon ammonium absorption liquid with proper concentration, the liquid in the reaction box is conveyed to the finished product storage box.

Description

Method and equipment for preparing ammonium bicarbonate type extraction liquid
Technical Field
The invention relates to the technical field of water treatment, in particular to a method and equipment for preparing a carbon ammonium draw solution.
Background
Forward osmosis refers to a process in which two kinds of aqueous solutions with different osmotic pressures are respectively placed on two sides of a forward osmosis membrane, and water molecules penetrate through the forward osmosis membrane from a low osmotic pressure side to a high osmotic pressure side under the driving of osmotic pressure difference. The driving force of the forward osmosis process is the osmotic pressure difference between the feed liquid and the draw liquid, so compared with membrane separation technologies such as reverse osmosis and nanofiltration, the forward osmosis technology has the advantages of low energy consumption, high recovery rate, light membrane pollution and the like, is an environment-friendly technology with great potential, and has the application range in the fields of seawater desalination, sewage purification, food, medicine, energy and the like.
In the last decade, the forward osmosis membrane and the separation technology thereof have been increasingly and internationally regarded as the most promising technology in the water treatment industry and the high-salinity water concentration technology. The forward osmosis membrane and the draw solution are two key factors influencing whether the forward osmosis technology can be successfully applied to the concentration of high-salinity water.
The ideal drawing liquid has higher solubility to ensure higher osmotic pressure, the effective components of the drawing liquid are easy to recover, the energy consumption of the recovery process is lower, the drawing liquid with low cost can be recycled, the drawing liquid has less pollution to the environment and does not chemically react with a membrane, and the drawing liquid used in the current commercialized forward osmosis project is mainly a carbon ammonium drawing liquid. The existing preparation method of the ammonium bicarbonate drawing liquid adopts ammonium bicarbonate and ammonia water, has high requirement on the purity of the ammonium bicarbonate and higher cost, the dissolution of the ammonium bicarbonate is an endothermic reaction, the influence of temperature on the solubility is great, the ammonium bicarbonate is easy to crystallize, and the ammonium bicarbonate is generally poured manually during the preparation, so the labor intensity is high. These factors greatly hinder the production efficiency of the ammonium carbonate-based drawing solution.
In view of the above, the present invention is particularly proposed.
Disclosure of Invention
The present invention is directed to a method and apparatus for preparing a carbon-based ammonium draw solution to solve the above-mentioned problems.
In order to achieve the above purpose of the present invention, the following technical solutions are adopted:
the equipment for preparing the ammonium bicarbonate drawing liquid comprises a reaction box, a circulating pump and CO 2 The device comprises a gas storage tank, an ejector, an absorption coil and a finished product storage tank;
the outlet and the inlet of the reaction box are respectively communicated with two ends of a pipeline to form an external circulation loop, and the pipeline is sequentially provided with a circulation pump, an ejector and an absorption coil pipe from the outlet to the inlet;
the inlet of the ejector is also connected with CO 2 The gas storage tanks are communicated;
the outlet of the reaction box is also communicated with the finished product storage box.
The equipment for preparing the ammonium bicarbonate type extracting solution has the advantages of simple structure, convenience in maintenance and easiness in operation.
The circulating pump exports aqueous ammonia or aqueous ammonia solution in with the reaction box by the pipeline, mixes with carbon dioxide gas on the pipeline, makes the absorption reaction more complete via the absorption coil pipe again, returns to in the reaction box again.
The absorption coil can increase ammonia water or ammonia water solution and CO 2 To promote thorough mixing and reaction of the two.
The ejector of the ejector is an ejector for gas-liquid mixing, and preferably, the ejector is a stainless steel ejector or an ejector made of PVDF (polyvinylidene fluoride) materials in order to ensure the strength of the ejector; in order to reduce or prevent the vibration of the ejector when gas and liquid are mixed, it is preferable that the ejector is fixed to the base.
Preferably, in the apparatus for preparing a carbon-containing ammonium extraction solution as described above, the reaction tank is connected to the finished product storage tank by a pump;
further preferably, the reaction tank is connected with the finished product storage tank through the circulating pump.
Will the reaction box through the circulating pump with the finished product bin links to each other can practice thrift a pump, makes the circulating pump obtain more abundant utilization.
Preferably, in the above equipment for preparing the ammonium bicarbonate type intake liquid, the absorption coil is formed by connecting 5 to 10 pipes with the length of 2m to 3m in series;
the absorption coil is formed by connecting 5, 6, 7, 8, 9 or 10 pipes with the length of 2m to 3m in series; the pipes are equal or unequal in length from 2m to 3m.
Further preferably, the tube of the absorption coil is a UPVC tube or a stainless steel tube;
both UPVC pipe and stainless steel pipe have the advantage of corrosion resistance, but stainless steel pipe has higher strength and better heat resistance, and therefore, most preferably, the pipe is stainless steel pipe.
Further preferably, two ends of the absorption coil are further provided with pipelines for short-circuiting the absorption coil.
The absorption coil pipe promotes ammonia water or ammonia water solution and CO 2 One of the main equipments for sufficient mixing and reaction requires regular maintenance, and short-circuiting pipes are provided at both ends thereof for the convenience of maintenance.
Preferably, in the above apparatus for preparing an ammonium carbonate-based draw solution, a heat exchanger is further disposed on the pipeline between the ejector and the absorption coil.
Due to ammonia water or ammonia water solution and CO 2 The reaction of (a) is exothermic, and therefore a heat exchanger is preferably provided for lowering the temperature.
Considering that the heat exchanger may not be needed to work when the temperature is lower in autumn and winter, and considering that the heat exchanger is convenient to overhaul, it is further preferable that pipelines for short-circuiting the heat exchanger are further arranged at two ends of the heat exchanger.
Preferably, the equipment for preparing a carbon ammonium based draw solution as described above, the heat exchanger is a plate heat exchanger or a tubular heat exchanger.
The plate heat exchanger has the advantages of small occupied area, high heat exchange efficiency, energy conservation and simple maintenance; the tubular heat exchanger has the advantages of high strength, larger heat exchange area and the like.
Preferably, in the apparatus for preparing an ammonium carbonate-based draw solution as described above, the pipeline between the outlet of the reaction tank and the heat exchanger is a stainless steel pipeline.
Preferably, in the above apparatus for preparing a carbon-ammonium extraction solution, a weighing module is disposed at the bottom of the reaction tank.
Wherein, in order to guarantee the stability of reaction box, preferably set up reaction box has a plurality of support columns, and the quantity of support column is 2, 3, 4, 5, 6 or more.
Preferably, the weighing module is provided with one or more weighing modules, and the weighing modules are arranged at the bottom of the supporting column.
The weighing module can accurately weigh the mass of ammonia water or ammonia water solution and introduced CO 2 And determining the gas quality so as to determine the proportion of the gas quality and the gas quality to obtain the carbon ammonium extraction liquid with proper concentration.
Preferably, in the above apparatus for preparing a carbon-ammonium extraction solution, an opening for injecting ammonia water or an ammonia water solution is provided at the top of the reaction tank;
preferably, the ammonia water or ammonia water solution is connected with the opening through an ammonia water delivery pump.
The method for preparing the ammonium bicarbonate draw solution by using the equipment comprises the following steps:
ammonia water or ammonia water solution is conveyed into the ejector through the circulating pump from the reaction box and is mixed with the CO 2 CO provided in a gas storage tank 2 After being mixed by the ejector, the mixture is further absorbed and reacted in the absorption coil pipe, then the mixture returns to the reaction box and is circulated, and after the reaction in the reaction box obtains carbon ammonium absorption liquid with proper concentration, the liquid in the reaction box is conveyed to the finished product storage box.
The concentration of the prepared drawing liquid can be regulated and controlled at any time, and the drawing liquid is clean and free of impurities.
Preferably, in the raw materials used in the invention, the ammonia water solution is prepared by adding reverse osmosis pure water into 23-25% industrial grade ammonia water, and the final ammonia water or ammonia water solution has a concentration of 6.9-11.5 mol/L; preferably, the CO is 2 Is industrial grade CO with the purity of more than 99.5 percent 2 A gas.
The main components of the carbon-ammonium draw solution prepared by the device are ammonium carbonate, ammonium bicarbonate, ammonium carbamate and other carbon-ammonium ion mixed solution;
preferably, the concentration of the finally prepared ammonium bicarbonate draw solution is 2-5 mol/L, and more preferably 2.8-3.5 mol/L;
preferably, the ratio of nitrogen element to carbon element in the finally prepared ammonium carbonate extracting solution is N: c =1.5 to 2.8, preferably 1.8 to 2.5.
Preferably, the method, the aqueous ammonia or aqueous ammonia solution and the CO are as described above 2 The gas is subjected to cooling treatment after being mixed by the ejector and before entering the absorption coil pipe for absorption, and the temperature of the mixed liquid before entering the absorption coil pipe cannot exceed 50 ℃; more preferably, the temperature of the mixed liquor before entering the absorption coil cannot exceed 45 ℃.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, and it is obvious that the drawings in the following description are some embodiments of the present invention, and other drawings can be obtained by those skilled in the art without creative efforts.
FIG. 1 is a schematic diagram of an apparatus for preparing a carbonaceous ammonium extraction solution according to the present invention.
Reference numerals are as follows:
an ammonia water delivery pump 1;
a reaction box 2;
CO 2 a gas storage tank 3;
a circulation pump 4;
an ejector 5;
a window 6;
an absorption coil 7;
a heat exchanger 8;
and (5) finished product storage boxes 9.
Detailed Description
Embodiments of the present invention will be described in detail below with reference to examples, but it will be understood by those skilled in the art that the following examples are only illustrative of the present invention and should not be construed as limiting the scope of the present invention. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are conventional products which are not indicated by manufacturers and are commercially available.
In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", etc., indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and simplicity of description, but do not indicate or imply that the device or element being referred to must have a particular orientation, be constructed and operated in a particular orientation, and thus, should not be construed as limiting the present invention. Furthermore, the terms "first," "second," and "third" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance.
In the description of the present invention, it should be noted that, unless otherwise explicitly specified or limited, the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either a fixed connection, a removable connection, or an integral connection; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meanings of the above terms in the present invention can be understood in specific cases to those skilled in the art.
As shown in fig. 1, the apparatus for preparing a carbon-ammonium extraction solution according to the present invention includes a reaction chamber 2; CO 2 2 A gas storage tank 3; a circulation pump 4; an ejector 5; an absorption coil 7 and a finished product storage tank 9;
an outlet and an inlet of the reaction box 2 are respectively communicated with two ends of a pipeline to form an external circulation loop, and the pipeline is sequentially provided with a circulation pump 4, an ejector 5 and an absorption coil 7 from the outlet to the inlet;
the ejector 5 is a tee joint and is also connected with CO 2 The gas storage tank 3 is communicated;
the outlet of the reaction box 2 is also communicated with the finished product storage box 9.
When the equipment is in operation, the circulating pump 4 outputs the ammonia water or ammonia water solution in the reaction tank 2 through the pipeline, and the ammonia water or ammonia water solution is connected with CO on the pipeline ejector 5 2 CO from gas tank 3 2 Mixing, leading the absorption reaction to be more complete through the absorption coil 7, and then returning the reaction product into the reaction box 2; the reaction is carried out along with ammonia water or ammonia water solution and CO 2 The operation in the pipeline is performed circularly, and after the reaction in the reaction tank 2 obtains the ammonium bicarbonate extraction liquid with proper concentration, the liquid in the reaction tank 2 can be conveyed into the finished product storage tank 9.
Preferably, the top of the reaction box 2 is provided with an opening for injecting ammonia water or an ammonia water solution; more preferably, the ammonia water or ammonia water solution is connected with the opening through an ammonia water delivery pump 1; more preferably, as shown in fig. 1, a pressure gauge and an on-off valve are further provided in series near the ammonia water feed pump 1.
In the reaction raw materials used in the method, the ammonia water solution is preferably prepared by adding reverse osmosis pure water into industrial-grade ammonia water with the concentration of 23-25%, and the final ammonia water or ammonia water solution has the concentration of 6.9-11.5 mol/L; the CO is 2 The purity of the industrial grade CO is preferably more than 99.5% 2 A gas.
In order to ensure the strength of the ejector 5, preferably, the ejector 5 is a stainless steel ejector or an ejector made of PVDF.
In order to reduce or prevent the vibration of the ejector when the gas and the liquid are mixed, it is preferable that the ejector 5 is fixed to the base.
Preferably, in one embodiment of the present invention, the CO is 2 A pressure reducing valve is also arranged on the pipeline connecting section between the gas storage tank 3 and the ejector 5; more preferably, a gas flow meter is further arranged on the pipeline connecting section between the pressure reducing valve and the ejector 5; the operator can more conveniently control and/or monitor the CO through the pressure reducing valve and/or the gas flow meter 2 The pressure of the gas.
The absorption coil 7 can increase ammonia water or ammonia water solution and CO 2 To promote thorough mixing and reaction of the two; in order that the absorption coil 7 has a better absorption effect, preferably, the absorption coil is formed by connecting 5, 6, 7, 8, 9 or 10 pipes with the length of 2m to 3m in series; further preferably, the pipes are pipes with equal or unequal lengths from 2m to 3m.
In order to make the absorption coil 7 have better corrosion resistance, the tube of the absorption coil is preferably a UPVC tube or a stainless steel tube; in order to make the absorption coil 7 have better heat resistance and strength at the same time, it is more preferable that the tube of the absorption coil is a stainless steel tube.
The absorption coil 7 promotes ammonia water or ammonia water solution and CO 2 One of the main devices for thorough mixing and reaction requires periodic maintenance in order to maintain itConveniently, as shown in fig. 1, preferably, in an embodiment of the present invention, two ends of the absorption coil 7 are further provided with a pipe for short-circuiting the absorption coil 7; more preferably, the short-circuit pipeline is also provided with a switch valve for controlling the switch of the short-circuit pipeline; more preferably, in order to better realize the short-circuit effect, a check valve is further arranged in series at the inlet of the absorption coil 7 near the reaction tank 2, a switch valve is further arranged in series at the outlet of the absorption coil 7 near the reaction tank 2, and the check valve and the switch valve can be short-circuited together with the absorption coil 7. Wherein the purpose of the check valve is that when the absorption coil 7 is short-circuited, the solution does not flow back to the absorption coil 7.
Preferably, the ammonia or ammonia solution and the CO 2 The gas is subjected to temperature reduction treatment after being mixed by the ejector and before entering the absorption coil for absorption, and the temperature of the mixed liquid before entering the absorption coil cannot exceed 50 ℃; more preferably, the temperature of the mixed liquor before entering the absorption coil cannot exceed 45 ℃.
Due to ammonia water or ammonia water solution and CO 2 Is an exothermic reaction, and CO 2 Since the solubility of (b) is decreased due to the increase of the temperature, thereby affecting the reaction efficiency, it is preferable that a heat exchanger 8 is further provided on the pipe between the ejector 5 and the absorption coil 7 in one embodiment of the present invention.
Considering that the heat exchanger may not be needed to work when the temperature is low in autumn and winter and considering that the heat exchanger is convenient to overhaul, preferably, pipelines for short-circuiting the heat exchanger are further arranged at two ends of the heat exchanger; more preferably, the short-circuit pipeline is also provided with a switch valve for controlling the switch of the short-circuit pipeline; more preferably, in order to achieve the short-circuit effect better, a check valve is further connected in series at the inlet of the heat exchanger 8 close to the reaction tank 2, a switch valve is further connected in series at the outlet of the heat exchanger 8 close to the reaction tank 2, and the check valve and the switch valve can be short-circuited together with the heat exchanger 8. Wherein the purpose of the check valve is that when the heat exchanger 8 is short-circuited, the solution does not flow back to the heat exchanger 8.
Preferably, if the temperature of the mixed liquid before entering the absorption coil is higher than 50 ℃, the short circuit of the heat exchanger 8 is closed, so that the temperature of the mixed liquid is reduced through the heat exchanger 8 before entering the absorption coil. More preferably, as shown in fig. 1, in order to better monitor the temperature of the mixed liquid, a temperature transmitter is further arranged in series at the inlet of the heat exchanger 8 near the reaction tank 2; meanwhile, in order to monitor the temperature of the mixed liquid in the pipeline no matter whether the heat exchanger 8 is in short circuit or not, preferably, another temperature transmitter is arranged before the position of the short circuit pipeline of the ejector 5 and the heat exchanger 8.
Preferably, the heat exchanger is a plate heat exchanger or a tube heat exchanger.
Due to ammonia water or ammonia water solution and CO 2 The reaction of (2) is exothermic, and when the ambient temperature is high and the reaction is severe, the temperature of the pipeline between the outlet of the reaction box 2 and the heat exchanger 8 is often relatively high, so in order to ensure the use safety and stability of the device, the pipeline of the section is preferably made of stainless steel.
Preferably, the bottom of the reaction box 2 is provided with a weighing module.
The weighing module can accurately weigh the mass of ammonia water or ammonia water solution and introduced CO 2 And determining the gas quality so as to determine the proportion of the two to obtain the ammonium carbonate extracting solution with proper concentration.
The main components of the carbon ammonium extraction liquid prepared by the device are ammonium carbonate, ammonium bicarbonate, ammonium carbamate and other carbon ammonium ion mixed solutions; preferably, the concentration of the finally prepared ammonium bicarbonate draw solution is 2-5 mol/L, and more preferably 2.8-3.5 mol/L; preferably, the ratio of nitrogen element to carbon element in the finally prepared ammonium carbonate extracting solution is N: c =1.5 to 2.8, preferably 1.8 to 2.5.
In order to ensure the stability of the reaction box 2, it is preferable to arrange the reaction box to have a plurality of support columns, the number of the support columns being 2, 3, 4, 5, 6 or more. More preferably, the weighing module is provided with one or more weighing modules and is arranged at the bottom of the supporting column.
When the reaction is carried out for a period of time and the concentration of the ammonium carbonate extracting solution is appropriate, the reactant in the reaction tank 2 can be discharged into the finished product storage tank 9.
Preferably, in one embodiment of the present invention, said reaction tank 2 is connected to said product storage tank 9 by means of a pump; in order to make the circulation pump more fully utilized, it is more preferable that the reaction tank 2 is connected to the product storage tank 9 through the circulation pump 4.
Preferably, in one embodiment of the invention, the number of finished storage bins 9 may be 1, 2, 3, 4, 5, 6 or more.
Preferably, in order to better control the opening and closing of the finished product storage tank 9, as shown in fig. 1, a switching valve is further disposed on a direct pipeline between the reaction tank 2 and the finished product storage tank 9; more preferably, the on-off valve is provided in series with the product storage tank 9 on a branch of the main pipe in order that the on-off valve does not interfere with the reaction in the main pipe.
Preferably, in order to better judge whether the reaction is complete, a branch for sampling is further provided in the pipeline, and an on-off valve is also provided on the branch to control the on-off of the branch for sampling.
Preferably, as shown in fig. 1, in order to monitor the pressure at the outlet and the pipeline of the circulation pump 4 and prevent the liquid pressure when the ammonia water or the ammonia water solution in the reaction tank 2 is output through the circulation pump 4 and enters the ejector 5 from being too high or too low, a pressure gauge is further disposed on the pipeline between the circulation pump 4 and the ejector 5.
In order to observe the conditions in the pipeline conveniently, the ammonia water or the ammonia water solution and CO are observed visually 2 Whether or not mixing is complete, as shown in fig. 1, it is preferred that in one embodiment of the present invention, windows 6 are provided in the vicinity of the ejector 5, the absorption coil 7, and the heat exchanger 8, respectively.
Finally, it should be noted that: the above embodiments are only used to illustrate the technical solution of the present invention, and not to limit the same; while the invention has been described in detail and with reference to the foregoing embodiments, it will be understood by those skilled in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some or all of the technical features may be equivalently replaced; and the modifications or the substitutions do not make the essence of the corresponding technical solutions depart from the scope of the technical solutions of the embodiments of the present invention.

Claims (10)

1. The method for preparing the ammonium carbonate drawing liquid by using the equipment for preparing the ammonium carbonate drawing liquid is characterized by comprising the following steps of:
ammonia water is conveyed into the ejector from the reaction box through the circulating pump and is mixed with CO 2 CO provided in a gas storage tank 2 After being mixed by the ejector, the mixture is further absorbed and reacted in the absorption coil pipe, then the mixture returns to the reaction box and is circulated, and after the reaction in the reaction box obtains carbon ammonium absorption liquid with proper concentration, the liquid in the reaction box is conveyed to a finished product storage box;
the ammonia water and the CO 2 The gas is subjected to temperature reduction treatment after being mixed by the ejector and before entering the absorption coil for absorption, and the temperature of the mixed liquid before entering the absorption coil cannot exceed 50 ℃;
the equipment comprises a reaction tank, a circulating pump and CO 2 The device comprises a gas storage tank, an ejector, an absorption coil and a finished product storage tank;
an outlet and an inlet of the reaction box are respectively communicated with two ends of a pipeline to form an external circulation loop, and the pipeline is sequentially provided with a circulation pump, an ejector and an absorption coil pipe in the direction from the outlet to the inlet;
the inlet of the ejector is also connected with CO 2 The gas storage tanks are communicated;
the outlet of the reaction box is also communicated with the finished product storage box;
a weighing module is arranged at the bottom of the reaction tank;
the absorption coil is formed by serially connecting 5 to 10 pipes with the length of 2m to 3m;
and a heat exchanger is also arranged on a pipeline between the ejector and the absorption coil.
2. The method of claim 1, wherein the reaction tank is connected to the product storage tank by a pump.
3. The method of claim 2 wherein said reaction tank is connected to said product storage tank by said circulation pump.
4. The method of claim 1, wherein the tubing of the absorption coil is UPVC tubing or stainless steel tubing.
5. The method of claim 1, wherein the ends of the absorption coil are further provided with tubing for short circuiting the absorption coil.
6. The method of claim 1, wherein the heat exchanger is further provided with a pipe at both ends thereof for short-circuiting the heat exchanger.
7. The method of claim 1, wherein the heat exchanger is a plate heat exchanger or a tube heat exchanger.
8. The method of claim 1, wherein the conduit between the outlet of the reaction tank and the heat exchanger is a stainless steel conduit.
9. The method according to claim 1, characterized in that the top of the reaction tank is provided with an opening for injecting ammonia.
10. The method of claim 9, wherein the ammonia is connected to the opening by an ammonia transfer pump.
CN201610922145.6A 2016-10-21 2016-10-21 Method and equipment for preparing ammonium bicarbonate type extraction liquid Active CN106422994B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610922145.6A CN106422994B (en) 2016-10-21 2016-10-21 Method and equipment for preparing ammonium bicarbonate type extraction liquid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610922145.6A CN106422994B (en) 2016-10-21 2016-10-21 Method and equipment for preparing ammonium bicarbonate type extraction liquid

Publications (2)

Publication Number Publication Date
CN106422994A CN106422994A (en) 2017-02-22
CN106422994B true CN106422994B (en) 2022-10-18

Family

ID=58176004

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610922145.6A Active CN106422994B (en) 2016-10-21 2016-10-21 Method and equipment for preparing ammonium bicarbonate type extraction liquid

Country Status (1)

Country Link
CN (1) CN106422994B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107389589A (en) * 2017-08-03 2017-11-24 国网安徽省电力公司电力科学研究院 Detection absorption plant for sulfur hexafluoride gas
CN115536090B (en) * 2022-10-09 2024-04-12 深圳天华机器设备股份有限公司 Film-removing liquid medicine recovery device

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB731540A (en) * 1951-06-02 1955-06-08 Chemical Construction Corp Improvements relating to method of conducting chemical reactions and apparatus therefor
EP0860449A1 (en) * 1997-02-25 1998-08-26 CP TECH S.r.l. A continuous process for effecting gas liquid reactions
CN1276364A (en) * 1999-06-02 2000-12-13 奥克森诺奥勒芬化学股份有限公司 Method for carrying out heterogeneous catalytic reaction, especially hydroformylation
CN1330626A (en) * 1998-12-12 2002-01-09 巴斯福股份公司 Preparation of amines
CN1832979A (en) * 2003-06-06 2006-09-13 伊斯曼化学公司 Polyester process using a pipe reactor
CN204588716U (en) * 2015-04-23 2015-08-26 太原海力丰科技发展有限公司 A kind of pressurization tubular reactor utilizing melamine tail gas to produce ammonium nitrate solution

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2284638Y (en) * 1997-03-24 1998-06-24 化学工业部上海化工研究院 Desorption tower for thin ammonia water containing carbon dioxide
NL1008573C2 (en) * 1998-03-12 1999-09-14 Dsm Nv Device for carrying out gas / liquid contact.
CN2464427Y (en) * 2001-02-14 2001-12-12 李紫恩 High-energy wet type dust remover
US6797039B2 (en) * 2002-12-27 2004-09-28 Dwain F. Spencer Methods and systems for selectively separating CO2 from a multicomponent gaseous stream
GB0507269D0 (en) * 2005-04-11 2005-05-18 Johnson Matthey Plc Steam reforming
US8026380B2 (en) * 2007-07-30 2011-09-27 H R D Corporation System and process for production of fatty acids and wax alternatives from triglycerides
CN101497452A (en) * 2008-01-28 2009-08-05 刘键 Method for preparing ammonium acid carbonate using flue gas and equipment thereof
CN101513600B (en) * 2009-03-23 2012-01-18 江苏工业学院 Method for producing gas hydrate and device thereof
EP2377813B1 (en) * 2010-04-19 2014-12-31 Celanese International Corporation Method for the manufacture of an ammonium sulfate composition
CN102335573B (en) * 2010-07-23 2013-09-11 中国石油化工股份有限公司 Caprolactam causticization device
CN102030775B (en) * 2010-09-14 2012-08-08 浙江工业大学 Method for producing N-(N-butyl)thiophosphoric triamide in channelization manner and special equipment
WO2012121886A1 (en) * 2011-02-25 2012-09-13 Southern Company Dispersed bubble reactor for enhanced gas-liquid-solids contact and mass transfer
DE102011082441A1 (en) * 2011-09-09 2013-03-14 Evonik Oxeno Gmbh Jet loop reactor with nanofiltration
CN102728285B (en) * 2012-07-10 2014-05-28 四川大学 System and device for three-phase complete mixed flow carbon dioxide ammoniation mineralization reaction
CN102895844A (en) * 2012-10-10 2013-01-30 南昌航空大学 Liquid carbon dioxide absorbent and preparation method thereof
CN203790929U (en) * 2014-04-03 2014-08-27 湖北华世通生物医药科技有限公司 System for gas-liquid reaction
CN104353361A (en) * 2014-11-20 2015-02-18 淄博泰禾实业有限公司 Forward osmosis absorption liquid using and recycling method and forward osmosis absorption device
CN104478041B (en) * 2014-11-27 2016-01-20 新疆德蓝股份有限公司 A kind ofly just permeate for brackish water desalination the preparation method drawing liquid
CN104959353B (en) * 2015-07-07 2016-04-06 山东泰邦生物制品有限公司 A kind of on-line cleaning method of cooling type of economizing on water
CN105417566A (en) * 2015-11-26 2016-03-23 恩平粤怡化工有限公司 Method for preparing nano calcium carbonate through full-automatic rotating pressure jet-carbonation technology
CN105503568A (en) * 2016-01-28 2016-04-20 杭州海虹精细化工有限公司 Reaction system and method for compounding adipic acid by adopting loop reactor
CN206168390U (en) * 2016-10-21 2017-05-17 北京沃特尔水技术股份有限公司 Apparatus for preparing liquid is drawn to carbon ammonium class

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB731540A (en) * 1951-06-02 1955-06-08 Chemical Construction Corp Improvements relating to method of conducting chemical reactions and apparatus therefor
EP0860449A1 (en) * 1997-02-25 1998-08-26 CP TECH S.r.l. A continuous process for effecting gas liquid reactions
CN1330626A (en) * 1998-12-12 2002-01-09 巴斯福股份公司 Preparation of amines
CN1276364A (en) * 1999-06-02 2000-12-13 奥克森诺奥勒芬化学股份有限公司 Method for carrying out heterogeneous catalytic reaction, especially hydroformylation
CN1832979A (en) * 2003-06-06 2006-09-13 伊斯曼化学公司 Polyester process using a pipe reactor
CN204588716U (en) * 2015-04-23 2015-08-26 太原海力丰科技发展有限公司 A kind of pressurization tubular reactor utilizing melamine tail gas to produce ammonium nitrate solution

Also Published As

Publication number Publication date
CN106422994A (en) 2017-02-22

Similar Documents

Publication Publication Date Title
Ulbricht et al. Ammonia recovery from industrial wastewater by TransMembraneChemiSorption
CN106422994B (en) Method and equipment for preparing ammonium bicarbonate type extraction liquid
CN109455735B (en) Chemical pure ammonia water preparation system and method
CN102936201B (en) Production apparatus and production method for methyl nitrite
CN104591436A (en) Gas hydrate method sewage treatment system
CN202185260U (en) Forward osmosis equipment
Vogler et al. Biogas conditioning using hollow fiber membrane contactors
CN206168390U (en) Apparatus for preparing liquid is drawn to carbon ammonium class
CN103318921A (en) Method for preparing ammonium carbonate solution from ammonia-containing aqueous solution
CN111004387A (en) Method for preparing modified long carbon chain nylon by connecting multiple reactors in series
CN202666769U (en) Urea water production equipment for vehicle, ship or thermal power plant
CN204454761U (en) A kind of ultrafiltration injection water system
US20220126253A1 (en) Acrylamide production system
CN218665415U (en) Equipment for preparing hydrobromic acid by distillation with finished liquid as raw material
CN112010783B (en) Ammonolysis reaction system, taurine intermediate sodium taurate and preparation method of taurine
CN202566172U (en) Device used for increasing dissolved oxygen content in instant tea
CN103601648B (en) Desalination and purification method of pentasodium diethylenetriamine pentaacetic acid (DTPA)
CN203295267U (en) Carbon dioxide dissolving reaction device
CN113003884A (en) Green ammonia water recovery system based on anaerobic fermentation and membrane distillation
CN218089240U (en) High-salt concentration device and system for divalent salt
CN201848238U (en) Crude propylene glycol carbonizing apparatus in production of dimethyl carbonate
CN2892837Y (en) High-concentration industrial waste water processing system
CN204198528U (en) The Integrated Processing Unit of calcic suspended solid, chloride, salt bearing liquid wastes
CN112370971A (en) Separation and concentration method and separation and concentration device for food materials
CN212954701U (en) Lithium-containing wastewater recovery system

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant