CN113773173A - Production process and device of ultrapure isopropanol - Google Patents

Production process and device of ultrapure isopropanol Download PDF

Info

Publication number
CN113773173A
CN113773173A CN202111011272.8A CN202111011272A CN113773173A CN 113773173 A CN113773173 A CN 113773173A CN 202111011272 A CN202111011272 A CN 202111011272A CN 113773173 A CN113773173 A CN 113773173A
Authority
CN
China
Prior art keywords
rectifying tower
tower
isopropanol
microwave
product
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
CN202111011272.8A
Other languages
Chinese (zh)
Other versions
CN113773173B (en
Inventor
王俊
陈华
韩海松
戚律
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.)
Changzhou Jiangye Information Engineering Technology Co.,Ltd.
Original Assignee
Changzhou University
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 Changzhou University filed Critical Changzhou University
Priority to CN202111011272.8A priority Critical patent/CN113773173B/en
Publication of CN113773173A publication Critical patent/CN113773173A/en
Application granted granted Critical
Publication of CN113773173B publication Critical patent/CN113773173B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C07C29/80Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/88Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to the technical field of chemical separation, and discloses a production process and a device of ultrapure isopropanol, which comprises a first microfiltration device, a reaction rectifying tower, a standing tank, a second microfiltration device, a heater, a vapor-liquid separation tank, a microwave rectifying tower, a sub-boiling rectifying tower and a nanofiltration device which are sequentially connected; the reactive distillation tower is at least provided with 3 feed inlets, namely a feed inlet of an ion complexing agent, a feed inlet of an isopropanol raw material and a feed inlet of a microwave distillation tower top product; a baffle is arranged in the standing tank; a filler foam catching net is arranged in the vapor-liquid separation tank; the microwave rectifying tower comprises a secondary dehydration rectifying tower and a microwave generator, and the stripping section of the secondary dehydration rectifying tower is arranged in the microwave generator; the heating device of the sub-boiling rectifying tower is an infrared heating pipe. The invention has the beneficial effects that: the method can be used for separating ultrapure isopropanol products in batches, and the products have stable quality and are free from solid waste discharge.

Description

Production process and device of ultrapure isopropanol
Technical Field
The invention relates to a production process and a device of ultrapure isopropanol, in particular to a process and a device for producing high-purity isopropanol by removing metal ions and water through reactive distillation and microwave distillation, belonging to the technical field of chemical separation.
Background
Propylene hydration is currently the most common process for the commercial production of isopropanol worldwide. Isopropanol has intersolubility with water, fat compounds and many other organic matters, is an important organic chemical raw material and organic solvent, and has wide application in various fields. The ultrapure isopropanol is used as a chemical cleaning agent and is widely applied in the industrial field. With the leap forward of computer and mechatronic technologies, the information industry is the largest and most rapidly developing industry in world economy. The development of the information industry has driven a great demand for high purity reagents and other microelectronic chemicals. In the manufacturing process of the submicron ULSI silicon wafer, no matter the surface of the silicon wafer is treated after oxidation and etching, the film deposition and the high-temperature furnace diffusion are cleaned for many times by chemical cleaning agents prepared by a plurality of high-purity chemical reagents, and then cleaned by ultrapure water, and finally cleaned by an ultrapure isopropanol solvent in order to avoid leaving oil stains and water marks and achieve the purpose of quick drying.
Currently, ultrapure isopropanol is usually obtained by using industrial grade isopropanol as a raw material and performing dehydration, demetallization, purification and refining. Rectification is a main method for industrially purifying isopropanol and comprises azeotropic rectification, extractive rectification, salt-adding rectification and the like. However, the dehydration efficiency of the rectification cannot meet the water content requirement of the ultrapure isopropanol, and the metal ion and particle contents of the ultrapure isopropanol put forward very high requirements on the ultrapure isopropanol product, which cannot be met by the conventional rectification process.
In the prior art, dehydration (chemical or adsorption) and demetalization (metal complexing or ion exchange resin) are divided into two working sections, so that the process complexity is increased, the removal efficiency is reduced, a dehydrated solid waste product is formed, and the product quality can be unstable.
Disclosure of Invention
In order to overcome the defects of complex process flow, low removal efficiency, formation of dehydrated solid waste and unstable product quality in the prior art, the invention provides a process and a device for producing ultrapure isopropanol, integrates the process flow and the device for continuously and efficiently producing the ultrapure isopropanol product by strengthening demetallization and dehydration through reactive distillation and microwave distillation, can obtain the ultrapure isopropanol product through batch separation, and has stable product quality and no solid waste discharge.
In order to achieve the purpose, the invention provides the following technical scheme:
a production device of ultrapure isopropanol comprises a first microfiltration device, a reaction rectifying tower, a standing tank, a second microfiltration device, a heater, a vapor-liquid separation tank, a microwave rectifying tower, a sub-boiling rectifying tower and a nanofiltration device which are connected in sequence; the reactive distillation tower is at least provided with 3 feed inlets, namely a feed inlet of an ion complexing agent, a feed inlet of an isopropanol raw material and a feed inlet of a microwave distillation tower top product; a baffle is arranged in the standing tank; a filler foam catching net is arranged in the vapor-liquid separation tank; the microwave rectifying tower comprises a secondary dehydration rectifying tower and a microwave generator, and the stripping section of the secondary dehydration rectifying tower is arranged in the microwave generator; the heating device of the sub-boiling rectifying tower is an infrared heating pipe; the production device also comprises an ion exchange device, and a feed inlet of the ion exchange device is connected with the bottom of the vapor-liquid separation tank; the discharge hole of the ion exchange device is connected with the feed inlet of the ion complexing agent of the reaction rectifying tower.
Further, the first microfiltration device, the second microfiltration device and the nanofiltration device are commonly used filtering devices in the field of chemical separation, wherein the first microfiltration device and the second microfiltration device are used for filtering solid particles.
Furthermore, the number of reaction rectifying tower plates is 35-40, the complexing solvent is fed from the 5 th to 10 th plates, the isopropanol raw material is fed from the 15 th to 20 th plates, and the product at the top of the reaction rectifying tower is fed from the 25 th to 30 th plates.
Further, the ion complexing agent is 18-crown-6-ether solvent and a compound thereof.
Furthermore, the baffles arranged in the standing tank are arranged in a staggered mode at equal intervals, the interval between every two adjacent baffles is 300-600 mm, the tail end of each baffle is provided with a notch, and the length of each baffle is 100-300 mm.
Furthermore, chelating resin is filled in the ion exchange device, macroporous styrene ion exchange resin with iminodiacetic acid chelating groups and H-type strong acid cation resin RSO are filled in the order3 -1H+The liquid phases are sequentially passed in the above order, so that the divalent and higher metal ions and monovalent metal ions can be exchanged in a gradient manner with high efficiency.
Furthermore, the microwave rectifying tower is made of ceramic or quartz, ceramic packing or quartz packing is filled in the microwave rectifying tower, the number of tower plates is 25-35, 10-15 rectifying sections and 15-20 stripping sections are arranged in the microwave rectifying tower, and the microwave generator is arranged in 5 tower sections at the bottom of the stripping sections.
Furthermore, the material of the sub-boiling rectifying tower is high-purity quartz, the high-purity quartz random packing is filled in the tower, and the separation theoretical level is 10 blocks.
A production process of ultrapure isopropanol comprises the following specific steps: the industrial isopropanol raw material enters a first microfiltration device, enters a reaction rectifying tower after being filtered, isopropanol by-products are discharged from the top of the tower, tower bottom products are sent to a standing tank, the standing tower bottom products are sent to a second microfiltration device, the filtered products are sent to a heater to be heated until being partially vaporized, then the vaporized products are sent to a vapor-liquid separation tank, the products at the bottom of the tank are a mixture of ion complex salt and isopropanol and are sent to an ion exchange device to carry out ion exchange reaction, and reactants flowing out of the ion exchange device are circularly sent to the reaction rectifying tower; the gas-phase product at the top of the gas-liquid separation tank enters a microwave rectifying tower, the bottom of the microwave rectifying tower is heated by a microwave generator, the product at the top of the microwave rectifying tower is sent to a reaction rectifying tower, and the product at the bottom of the microwave rectifying tower is sent to a sub-boiling rectifying tower; the heating device of the sub-boiling rectifying tower is an infrared heating pipe, and a liquid-phase product flowing out of the bottom of the microwave rectifying tower is heated, vaporized and condensed and flows out of the top of the tower; and (3) filtering the liquid phase flowing out of the top of the sub-boiling rectification tower in a nanofiltration device to obtain an ultra-pure isopropanol product.
Further, the tower top pressure of the reactive distillation tower is 0.35-1.5 atm, the reflux ratio is 1-3, the operating temperature is 60-90 ℃, and the mass ratio of the dosage of the metal complexing agent which is sent into the reactive distillation tower and used for removing the metal ions in the isopropanol solution through the complexing reaction is 0.1-0.5% of the feeding quantity of the isopropanol.
Further, a product at the bottom of the reactive distillation tower enters from the bottom of a standing tank and flows out from the top of the standing tank, the retention time in the standing tank is guaranteed to be 20-40 min, and the operating temperature is 60-90 ℃; the operating pressure of the vapor-liquid separation tank is 0.1MPa to 0.2MPa, and the operating temperature is 80 ℃ to 100 ℃.
Further, the operating pressure of the ion exchange device is 0.1-0.2 MPa, and the operating temperature is 60-90 ℃.
Further, the pressure of the microwave rectifying tower is 0.1-0.2 MPa, the operating temperature is 80-100 ℃, the microwave frequency is 2400-2500 MHz, the product at the top of the tower returns to the reaction rectifying tower, and the product at the bottom of the tower enters the sub-boiling rectifying tower.
Further, the operating pressure of the sub-boiling rectifying tower is 0.06-0.09 MPa, the operating temperature is 35-50 ℃, the reflux ratio is 0.1-0.5, and the product at the top of the tower is sent to a nanofiltration device for filtration to obtain the ultra-pure isopropanol product.
Compared with the prior art, the separation device and the separation process for the maleic anhydride hydrogenation product have the following beneficial effects:
(1) the production process and the device can separate the ultrapure isopropanol product in batches, and the product has stable quality and no solid waste discharge.
(2) The production process and the device of the invention use reactive distillation to simultaneously remove metal ions and water, thereby improving the separation efficiency and reducing the process complexity.
(3) The production process and the device adopt microwave rectification to strengthen dehydration, and because the polarity of water molecules is 10.2 which is 3.9 greater than that of isopropanol, the water molecules are easier to volatilize during microwave heating, thereby improving the volatilization performance of water. The production process and the device can further remove water to purify the isopropanol under the conditions of no introduction of an extracting agent to pollute the isopropanol, short time consumption and low cost, improve the stability of products, and enhance the dehydration efficiency and the dehydration quality, and the ultrapure isopropanol obtained by the production process has the isopropanol content of more than 99.99 percent, the water content of less than 50ppm, the cation content of less than 0.1ppb and the anion content of less than 50ppb and meets the SEMI C12 standard.
Drawings
FIG. 1 is a flow chart of the apparatus and process for producing ultrapure isopropanol of the present invention.
The reference numerals in the figures have the meaning: 1-a first microfiltration device; 2-a reactive distillation column; 3-standing the tank; 4-a second microfiltration device; 5-a heater; 6-vapor-liquid separation tank; 7-a secondary dehydration rectifying tower; 8-a microwave generator; 9-a sub-boiling rectification column; 10-a nanofiltration device; 11-ion exchange unit.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
As shown in fig. 1, the apparatus for producing ultrapure isopropanol provided by the present invention comprises a first microfiltration device 1, a reactive distillation column 2, a standing tank 3, a second microfiltration device 4, a heater 5, a vapor-liquid separation tank 6, a microwave distillation column, a sub-boiling distillation column 9 and a nanofiltration device 10, which are connected in sequence; the reactive distillation tower 2 is at least provided with 3 feed inlets, namely a feed inlet of an ion complexing agent, a feed inlet of an isopropanol raw material and a feed inlet of a microwave distillation tower top product; a baffle is arranged in the standing tank 3; a filler foam catching net is arranged in the vapor-liquid separation tank 6; the microwave rectifying tower comprises a secondary dehydration rectifying tower 7 and a microwave generator 8, and the stripping section of the secondary dehydration rectifying tower 7 is arranged in the microwave generator 8; the heating device of the sub-boiling rectifying tower 9 is an infrared heating pipe; the production device also comprises an ion exchange device 11, and a feed inlet of the ion exchange device 11 is connected with the bottom of the vapor-liquid separation tank 6; the discharge hole of the ion exchange device 11 is connected with the feed inlet of the ion complexing agent of the reaction rectifying tower.
In a specific implementation manner of this embodiment, the number of plates of the reactive distillation column 2 is 35 to 40, the complexing solvent is fed from the 5 th to 10 th plates, the isopropyl alcohol raw material is fed from the 15 th to 20 th plates, and the overhead product of the reactive distillation column 2 is fed from the 25 th to 30 th plates.
In a specific embodiment of this example, the ion complexing agent is 18-crown-6-ether solvent and its complex.
In a specific embodiment of this embodiment, the baffles arranged in the standing tank 3 are arranged in an equidistant staggered manner, the distance between two adjacent baffles is 300-600 mm, the end of each baffle is provided with a notch, and the length of each baffle is 100-300 mm.
In a specific embodiment of this embodiment, the ion exchange device 11 is filled with chelating resin, macroporous styrene ion exchange resin with iminodiacetic acid chelating group, H-type strong acid cation resin RSO3 -1H+The liquid phases are sequentially passed in the above order, so that the divalent and higher metal ions and monovalent metal ions can be exchanged in a gradient manner with high efficiency.
In a specific embodiment of this embodiment, the microwave rectification tower is made of ceramic or quartz, and the microwave rectification tower is filled with ceramic packing or quartz packing, and has 25 to 35 tower plates, wherein the rectification section comprises 10 to 15 rectifying sections, the stripping section comprises 15 to 20 stripping sections, and the microwave generator 8 is disposed in the 5 tower sections at the bottom of the stripping section.
In a specific embodiment of this embodiment, the material of the sub-boiling rectification column 9 is high-purity quartz, the column contains high-purity quartz random packing, and the separation theoretical stage is 10 blocks.
As shown in fig. 1, the invention also provides a production process of the ultrapure isopropanol, which comprises the following specific steps: the industrial isopropanol raw material enters a first microfiltration device 1, enters a reaction rectifying tower 2 after being filtered, isopropanol by-products are discharged from the top of the tower, tower bottom products are sent to a standing tank 3, the standing tower bottom products are sent to a second microfiltration device 4, the filtered products are sent to a heater 5 to be heated until being partially vaporized, then the vaporized products are sent to a vapor-liquid separation tank 6, the products at the bottom of the tank are a mixture of ion complex salt and isopropanol and are sent to an ion exchange device 11 to carry out ion exchange reaction, and reactants flowing out of the ion exchange device 11 are circularly sent to the reaction rectifying tower 2; the gas-phase product at the top of the gas-liquid separation tank 6 enters a microwave rectifying tower, the bottom of the microwave rectifying tower is heated by a microwave generator 8, the product at the top of the microwave rectifying tower is sent to a reaction rectifying tower 2, and the product at the bottom of the microwave rectifying tower is sent to a sub-boiling rectifying tower 9; the heating device of the sub-boiling rectifying tower 9 is an infrared heating pipe, and a liquid-phase product flowing out of the bottom of the microwave rectifying tower is condensed and flows out of the top of the tower after being heated and vaporized; and (3) filtering the liquid phase flowing out of the top of the sub-boiling rectifying tower 9 in a nano-filtration device 10 to obtain an ultra-pure isopropanol product.
In a specific embodiment of this embodiment, the top pressure of the reactive distillation column 2 is 0.35 to 1.5atm, the reflux ratio is 1 to 3, the operating temperature is 60 to 90 ℃, and the mass ratio of the amount of the metal complexing agent fed into the reactive distillation column 2 for removing metal ions in the isopropanol solution by a complexation reaction is 0.1 to 0.5% of the feeding amount of the isopropanol.
In a specific implementation manner of the embodiment, a product at the bottom of the reactive distillation column 2 enters from the bottom of the standing tank 3 and flows out from the top of the standing tank, so that the standing time in the standing tank 3 is ensured to be 20-40 min, and the operating temperature is 60-90 ℃; the operation pressure of the vapor-liquid separation tank 6 is 0.1MPa to 0.2MPa, and the operation temperature is 80 ℃ to 100 ℃.
In a specific embodiment of this embodiment, the operating pressure of the ion exchange device 11 is 0.1MPa to 0.2MPa, and the operating temperature is 60 ℃ to 90 ℃.
In a specific embodiment of this embodiment, the microwave rectification tower has a pressure of 0.1MPa to 0.2MPa, an operating temperature of 80 to 100 ℃, a microwave frequency of 2400 to 2500MHz, the tower top product returns to the reactive rectification tower 2, and the tower bottom product enters the sub-boiling rectification tower 9.
In a specific embodiment of this embodiment, the operating pressure of the sub-boiling distillation column 9 is 0.06-0.09 MPa, the operating temperature is 35-50 ℃, the reflux ratio is 0.1-0.5, and the product at the top of the column is sent to the nanofiltration device 10 for filtration to obtain the ultrapure isopropanol product.
Example 1
Firstly, filtering industrial grade isopropanol (98%) raw material by a grade-1 microfilter, then feeding the raw material into a reaction rectifying tower with 36 theoretical plates, feeding a metal ion complexing agent which is 0.15% (mass ratio) of the feeding amount of the isopropanol into the reaction rectifying tower, wherein the metal ion complexing agent is 18-crown-6-ether solvent and a compound thereof, the operating pressure of the reaction rectifying tower is 0.5atm, the reflux ratio is 1.5, carrying out reaction rectification to obtain an isopropanol byproduct with the tower top of 90%, the tower top is an isopropanol metal complex salt reaction liquid with the water content of 99.5%, the reaction liquid is fed into a standing tank to stand for 25min, the operating temperature is 63.5 ℃, the reaction liquid is filtered by a grade-2 microfilter and then is fed into a heater to be heated, the heating material flow is fed into a steam-liquid separation tank, the operating temperature is 0.1MPa, the operating temperature is 85 ℃, wherein the liquid phase flowing out of the bottom of the steam-liquid separation tank is fed into macroporous styrene ion exchange resin sequentially filled with an imine diacetic acid group, h type strong acid cation resin RSO3 -1H+The ion exchange device regenerates the metal complexing agent, the operating pressure is 0.1MPa, the operating temperature is 65 ℃, and the exchanged metal complexing agent subjected to ion exchange returns to the reactive rectifying tower to form circulation; and (2) feeding the product at the top of the vapor-liquid separation tank into a rectifying tower with a theoretical plate number of 26 microwaves, wherein the operating pressure is 0.12MPa, the reflux ratio is 4, the microwave frequency is 2400MHz, 99% of isopropanol solution is extracted from the top of the tower and returned to the reactive rectifying tower, 99.99% of isopropanol is extracted from the bottom of the tower, the product at the bottom of the tower is fed into a sub-boiling rectifying tower with a theoretical plate number of 10, the pressure is 0.065MPa, the operating temperature is 50 ℃, the reflux ratio is 0.12, and the material flow extracted from the top of the tower is filtered by a nano-filtration device to obtain an ultra-pure isopropanol product. The samples were analyzed and the analytical data are shown in Table 1.
TABLE 1
Figure BDA0003238550310000081
Figure BDA0003238550310000091
Example 2
Firstly, filtering industrial grade isopropanol (98%) raw material by a 1-grade microfilter, then feeding the raw material into a reaction rectifying tower with 38 theoretical plates, feeding a metal ion complexing agent which is 0.35% (mass ratio) of the feeding amount of the isopropanol into the reaction rectifying tower, wherein the metal ion complexing agent is 18-crown-6-ether solvent and a compound thereof, the operating pressure of the reaction rectifying tower is 1atm, the reflux ratio is 2, carrying out reactive rectification to obtain an isopropanol byproduct with the tower top of 90%, the tower top is an isopropanol metal complex salt reaction solution with the water content of 99.5%, feeding the reaction solution into a standing tank, standing for 30min, the operating temperature is 83.5 ℃, filtering the reaction solution by a 2-grade microfilter, then feeding the heated material flow into a steam-liquid separation tank, the operating temperature is 0.15MPa, the operating temperature is 90 ℃, feeding a liquid phase flowing out of the bottom of the steam-liquid separation tank into a macroporous styrene ion exchange resin sequentially filled with an iminodiacetic acid base, h type strong acid cation resin RSO3 -1H+The ion exchange device regenerates the metal complexing agent, the operating pressure is 0.15, the operating temperature is 90 ℃, and the exchanged metal complexing agent after ion exchange returns to the reactive rectifying tower to form circulation; the product at the top of the vapor-liquid separation tank is sent into a rectifying tower with a theoretical plate number of 30 microwaves, the operating pressure is 0.12MPa, the reflux ratio is 5, the microwave frequency is 2450MHz, 99% of isopropanol solution is extracted from the top of the tower and returned to the reactive rectifying tower, 99.99% of isopropanol is extracted from the bottom of the tower, the product at the bottom of the tower is sent into a sub-boiling rectifying tower with a theoretical plate number of 10, the pressure is 0.075MPa, the operating temperature is 60 ℃, the reflux ratio is 0.3, and the material flow extracted from the top of the tower is filtered by a nano-filtration device to obtain an ultra-pure isopropanol product. The samples were analyzed and the analytical data are shown in Table 1.
Example 3
Firstly, filtering industrial isopropanol (98%) raw material by using 1-grade microfilter, then feeding the filtered raw material into 40 reaction rectifying towers whose theoretical plate number is 40, feeding metal ion complexing agent which is 18-crown-6-ether solvent and its composite solvent into the reaction rectifying tower, and feeding the metal ion complexing agent into the reaction rectifying tower, and making the metal ion complexing agent be 0.5% of isopropanol feeding quantityThe method comprises the steps of feeding reaction liquid into a standing tank for standing for 40min at an operating temperature of 90 ℃, filtering the reaction liquid by a 2-stage microfilter, heating the reaction liquid by a heater, feeding the heated material flow into a vapor-liquid separation tank at an operating pressure of 0.15MPa and an operating temperature of 100 ℃, feeding liquid phase flowing out of the bottom of the vapor-liquid separation tank into macroporous styrene ion exchange resin and H-type strong acid cation resin RSO, wherein the operating pressure of the reaction distillation column is 1.5atm, the reflux ratio is 3, the reaction distillation column obtains an isopropanol byproduct with a content of 90% at the top of the column, the isopropanol metal complex salt reaction liquid with a water content of 99.5% at the top of the column is fed into the standing tank, the operating temperature is 90 ℃, the heated material flow is fed into the heater for heating after being filtered by the 2-stage microfilter, the heated material flow is fed into the vapor-liquid separation tank, the operating pressure is 0.15MPa, and the operating temperature is 100 ℃, and the liquid phase flowing out of the bottom of the vapor-liquid phase from the bottom of the vapor-liquid separation tank is fed into macroporous styrene ion exchange resin and the H-type strong acid cation resin RSO3 -1H+The ion exchange device regenerates the metal complexing agent, the operating pressure is 0.2, the operating temperature is 90 ℃, and the exchanged metal complexing agent after ion exchange returns to the reactive rectifying tower to form circulation; and (2) feeding the product at the top of the vapor-liquid separation tank into a rectifying tower with the theoretical plate number of 35 microwaves, wherein the operating pressure is 0.2MPa, the reflux ratio is 15, the microwave frequency is 2500MHz, 99% of isopropanol solution is extracted from the top of the tower and returned to the reactive rectifying tower, 99.99% of isopropanol is extracted from the bottom of the tower, the product at the bottom of the tower is fed into a sub-boiling rectifying tower with the theoretical plate number of 10, the pressure is 0.09MPa, the operating temperature is 70 ℃, the reflux ratio is 0.5, and the material flow extracted from the top of the tower is filtered by a nano-filtration device to obtain an ultra-pure isopropanol product. The samples were analyzed and the analytical data are shown in Table 1.
It is noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other identical elements in a process, method, article, or apparatus that comprises the element.
Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

Claims (13)

1. An apparatus for producing ultrapure isopropanol, characterized in that: comprises a first microfiltration device, a reaction rectifying tower, a standing tank, a second microfiltration device, a heater, a vapor-liquid separation tank, a microwave rectifying tower, a sub-boiling rectifying tower and a nanofiltration device which are connected in sequence; the reactive distillation tower is at least provided with 3 feed inlets, namely a feed inlet of an ion complexing agent, a feed inlet of an isopropanol raw material and a feed inlet of a microwave distillation tower top product; a baffle is arranged in the standing tank; a filler foam catching net is arranged in the vapor-liquid separation tank; the microwave rectifying tower comprises a secondary dehydration rectifying tower and a microwave generator, and the stripping section of the secondary dehydration rectifying tower is arranged in the microwave generator; the heating device of the sub-boiling rectifying tower is an infrared heating pipe; the production device also comprises an ion exchange device, and a feed inlet of the ion exchange device is connected with the bottom of the vapor-liquid separation tank; the discharge hole of the ion exchange device is connected with the feed inlet of the ion complexing agent of the reaction rectifying tower.
2. The apparatus for the production of ultrapure isopropanol according to claim 1, wherein: the number of the reaction rectifying tower plates is 35-40, the complexing solvent is fed from the 5 th to 10 th plates, the isopropanol raw material is fed from the 15-20 th plates, and the product at the top of the reaction rectifying tower is fed from the 25 th to 30 th plates.
3. The apparatus for the production of ultrapure isopropanol according to claim 1, wherein: the ion complexing agent is 18-crown-6-ether solvent and a compound thereof.
4. The apparatus for the production of ultrapure isopropanol according to claim 1, wherein: the baffle that sets up in the jar of stewing is equidistant staggered arrangement, and two adjacent baffles interval is 300 ~ 600mm, and every baffle end is equipped with the breach, and length is 100 ~ 300 mm.
5. The apparatus for the production of ultrapure isopropanol according to claim 1, wherein: the ion exchange device is internally provided with chelating resin, macroporous styrene ion exchange resin with iminodiacetic acid chelating groups and H-type strong acid cation resin RSO3 -1H+The liquid phases are sequentially passed through the liquid phase separator according to the sequence.
6. The apparatus for the production of ultrapure isopropanol according to claim 1, wherein: the microwave rectifying tower is made of ceramic or quartz, ceramic packing or quartz packing is filled in the microwave rectifying tower, the number of tower plates is 25-35, 10-15 rectifying sections and 15-20 stripping sections are arranged in the microwave rectifying tower, and a microwave generator is arranged in 5 tower sections at the bottom of each stripping section.
7. The apparatus for the production of ultrapure isopropanol according to claim 1, wherein: the material of the sub-boiling rectifying tower is high-purity quartz, high-purity quartz random packing is filled in the tower, and the separation theoretical level is 10.
8. A production process of ultrapure isopropanol is characterized in that: the method comprises the following steps: the industrial isopropanol raw material enters a first microfiltration device, enters a reaction rectifying tower after being filtered, isopropanol by-products are discharged from the top of the tower, tower bottom products are sent to a standing tank, the standing tower bottom products are sent to a second microfiltration device, the filtered products are sent to a heater to be heated until being partially vaporized, then the vaporized products are sent to a vapor-liquid separation tank, the products at the bottom of the tank are a mixture of ion complex salt and isopropanol and are sent to an ion exchange device to carry out ion exchange reaction, and reactants flowing out of the ion exchange device are circularly sent to the reaction rectifying tower; the gas-phase product at the top of the gas-liquid separation tank enters a microwave rectifying tower, the bottom of the microwave rectifying tower is heated by a microwave generator, the product at the top of the microwave rectifying tower is sent to a reaction rectifying tower, and the product at the bottom of the microwave rectifying tower is sent to a sub-boiling rectifying tower; the heating device of the sub-boiling rectifying tower is an infrared heating pipe, and a liquid-phase product flowing out of the bottom of the microwave rectifying tower is heated, vaporized and condensed and flows out of the top of the tower; and (3) filtering the liquid phase flowing out of the top of the sub-boiling rectification tower in a nanofiltration device to obtain an ultra-pure isopropanol product.
9. The process for the production of ultrapure isopropanol according to claim 8, wherein: the tower top pressure of the reactive distillation tower is 0.35-1.5 atm, the reflux ratio is 1-3, the operating temperature is 60-90 ℃, and the mass ratio of the metal complexing agent is 0.1-0.5% of the feeding amount of the isopropanol.
10. The process for the production of ultrapure isopropanol according to claim 8, wherein: the product at the bottom of the reactive distillation tower enters from the bottom of the standing tank and flows out from the top of the standing tank, the retention time in the standing tank is guaranteed to be 20-40 min, and the operating temperature is 60-90 ℃; the operating pressure of the vapor-liquid separation tank is 0.1MPa to 0.2MPa, and the operating temperature is 80 ℃ to 100 ℃.
11. The process for the production of ultrapure isopropanol according to claim 8, wherein: the operating pressure of the ion exchange device is 0.1-0.2 MPa, and the operating temperature is 60-90 ℃.
12. The process for the production of ultrapure isopropanol according to claim 8, wherein: the pressure of the microwave rectifying tower is 0.1-0.2 MPa, the operating temperature is 80-100 ℃, the microwave frequency is 2400-2500 MHz, the product at the top of the tower returns to the reactive rectifying tower, and the product at the bottom of the tower enters the sub-boiling rectifying tower.
13. The process for the production of ultrapure isopropanol according to claim 8, wherein: the operating pressure of the sub-boiling rectifying tower is 0.06-0.09 MPa, the operating temperature is 35-50 ℃, the reflux ratio is 0.1-0.5, and the product at the top of the tower is sent to a nanofiltration device for filtration to obtain the ultra-pure isopropanol product.
CN202111011272.8A 2021-08-31 2021-08-31 Production process and device of ultrapure isopropanol Active CN113773173B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111011272.8A CN113773173B (en) 2021-08-31 2021-08-31 Production process and device of ultrapure isopropanol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111011272.8A CN113773173B (en) 2021-08-31 2021-08-31 Production process and device of ultrapure isopropanol

Publications (2)

Publication Number Publication Date
CN113773173A true CN113773173A (en) 2021-12-10
CN113773173B CN113773173B (en) 2022-09-16

Family

ID=78840196

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111011272.8A Active CN113773173B (en) 2021-08-31 2021-08-31 Production process and device of ultrapure isopropanol

Country Status (1)

Country Link
CN (1) CN113773173B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114470958A (en) * 2022-02-15 2022-05-13 北京袭明科技有限公司 Production method and device of high-purity electronic grade methanol
CN115322074A (en) * 2022-07-06 2022-11-11 晶瑞(湖北)微电子材料有限公司 Purification method of isopropanol

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2000292C1 (en) * 1991-10-29 1993-09-07 Нижнекамское производственное объединение "Нижнекамскнефтехим" Method of extracting and purifying of secondary butyl alcohol
US20040158108A1 (en) * 2003-02-06 2004-08-12 Snoble Karel A.J. Purification of alcohol
CN101362675A (en) * 2008-09-16 2009-02-11 江阴市润玛电子材料有限公司 Method for preparing super-clean and high-purity isopropanol and apparatus thereof
CN102249850A (en) * 2011-05-31 2011-11-23 无锡市东风化工厂 Method for preparing high-purity isopropanol
CN102690172A (en) * 2011-03-25 2012-09-26 中国石油化工股份有限公司 Method for producing isopropanol by acetone hydrogenation
CN106984058A (en) * 2017-05-09 2017-07-28 西南石油大学 A kind of small microwave heats continuous rectification apparatus
CN107021872A (en) * 2017-05-10 2017-08-08 天津九源化工工程有限公司 A kind of process for separation and purification of aqueous isopropanol
CN107253901A (en) * 2017-07-26 2017-10-17 四川天采科技有限责任公司 A kind of separation of high-purity isopropanol and purification method
CN111039759A (en) * 2019-11-22 2020-04-21 苏州博洋化学股份有限公司 Preparation method of ultra-clean high-purity isopropanol
CN111574326A (en) * 2020-04-29 2020-08-25 镇江润晶高纯化工科技股份有限公司 Purification method of semiconductor grade isopropanol

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2000292C1 (en) * 1991-10-29 1993-09-07 Нижнекамское производственное объединение "Нижнекамскнефтехим" Method of extracting and purifying of secondary butyl alcohol
US20040158108A1 (en) * 2003-02-06 2004-08-12 Snoble Karel A.J. Purification of alcohol
CN101362675A (en) * 2008-09-16 2009-02-11 江阴市润玛电子材料有限公司 Method for preparing super-clean and high-purity isopropanol and apparatus thereof
CN102690172A (en) * 2011-03-25 2012-09-26 中国石油化工股份有限公司 Method for producing isopropanol by acetone hydrogenation
CN102249850A (en) * 2011-05-31 2011-11-23 无锡市东风化工厂 Method for preparing high-purity isopropanol
CN106984058A (en) * 2017-05-09 2017-07-28 西南石油大学 A kind of small microwave heats continuous rectification apparatus
CN107021872A (en) * 2017-05-10 2017-08-08 天津九源化工工程有限公司 A kind of process for separation and purification of aqueous isopropanol
CN107253901A (en) * 2017-07-26 2017-10-17 四川天采科技有限责任公司 A kind of separation of high-purity isopropanol and purification method
CN111039759A (en) * 2019-11-22 2020-04-21 苏州博洋化学股份有限公司 Preparation method of ultra-clean high-purity isopropanol
CN111574326A (en) * 2020-04-29 2020-08-25 镇江润晶高纯化工科技股份有限公司 Purification method of semiconductor grade isopropanol

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
朱斌等: "工业级异丙醇连续生产电子级异丙醇", 《天然气化工(C1化学与化工)》 *
羊俊等: "常压下微量水-正丁醇汽液相平衡研究", 《化学工程》 *
胡湖生: "用填料塔将异丙醇连续共沸精馏脱水", 《浙江化工》 *
连峰等: "异丙醇脱水工艺技术进展", 《现代化工》 *
郑旭熙,杜长海主编: "《化工原理(第二版)下册》", 31 January 2016, 华中科技大学出版社 *
顾小焱等: "超纯异丙醇的制备方法研究", 《化学试剂》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114470958A (en) * 2022-02-15 2022-05-13 北京袭明科技有限公司 Production method and device of high-purity electronic grade methanol
CN115322074A (en) * 2022-07-06 2022-11-11 晶瑞(湖北)微电子材料有限公司 Purification method of isopropanol
CN115322074B (en) * 2022-07-06 2024-02-20 晶瑞(湖北)微电子材料有限公司 Purification method of isopropanol

Also Published As

Publication number Publication date
CN113773173B (en) 2022-09-16

Similar Documents

Publication Publication Date Title
CN113773173B (en) Production process and device of ultrapure isopropanol
CN105016554B (en) Semi-coke wastewater treatment process
JP2003512930A (en) Process for purifying industrial wastewater from propylene oxide production process
CN108059597B (en) Method and device for producing ethyl acetate by integrating reactive distillation and pervaporation
CN108128826B (en) Nitric acid-containing wastewater treatment device and treatment method
CN102502500A (en) Device for producing hydrogen chloride by resolving hydrochloric acid
CN108658051B (en) Method and device for recovering nitration waste acid and sulfuric acid recovered by method and device
CN113443977A (en) Sulfur and chlorine removal process in 2-ethyl anthraquinone production
CN111253284B (en) Benzyl cyanide production device and process with continuous whole process
CN110845734B (en) System and method for hydrolyzing organochlorosilane and refining hydrochloric acid
CN103772185B (en) Device and method for removing moisture and heteroacids in acetic acid
CN111892525A (en) N-methyl pyrrolidone for liquid crystal panel and production process thereof
TWI801674B (en) How to make isopropanol
CN103288135B (en) Filament wire is containing the method for chemical composition secondary resource whole in molybdenum spent acid
CN112047832A (en) N, N-dimethylacetamide wastewater recovery process
WO2010066017A1 (en) Process for purifying waste sulfuric acid
KR20210051943A (en) Continuous multi-stage treatment apparatus for separating and recovering phosphoric acid from mixed waste acid and as the same method
CN101245044A (en) Method for extracting biphenyl and indole from coal tar recovered wash oil
CN105329864A (en) Resourceful treatment method of waste acid solution in nitrobenzene production process
EP0118475A1 (en) Process for recovery of amine from spent acid stripping liquor
CN110606798A (en) Method for preparing benzyl alcohol by using microchannel reactor without alkali
CN113860995B (en) Recovery treatment process and treatment device for waste liquid produced in production of acetochlor
CN216798744U (en) Intermittent rectification and purification device for dimethyl sulfoxide
CN217472733U (en) Trioxymethylene's response device and production system thereof
CN108623474A (en) It is a kind of to purify N, N, N, the method for N- tetramethyl-1,3-propane diamines using azeotropic distillation

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
TR01 Transfer of patent right

Effective date of registration: 20221117

Address after: 213164 A401-402, Science and Technology Building, Jiangsu Research Institute, Dalian University of Technology, Changzhou Science and Education City, No. 18, Changwu Middle Road, Wujin District, Changzhou City, Jiangsu Province

Patentee after: Changzhou Jiangye Information Engineering Technology Co.,Ltd.

Address before: Gehu Lake Road Wujin District 213164 Jiangsu city of Changzhou province No. 1

Patentee before: CHANGZHOU University

TR01 Transfer of patent right