WO2024049101A1 - 고순도 (메트)아크릴산의 제조방법 - Google Patents

고순도 (메트)아크릴산의 제조방법 Download PDF

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WO2024049101A1
WO2024049101A1 PCT/KR2023/012550 KR2023012550W WO2024049101A1 WO 2024049101 A1 WO2024049101 A1 WO 2024049101A1 KR 2023012550 W KR2023012550 W KR 2023012550W WO 2024049101 A1 WO2024049101 A1 WO 2024049101A1
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meth
acrylic acid
tower
absorption
absorption tower
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PCT/KR2023/012550
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English (en)
French (fr)
Korean (ko)
Inventor
유성진
장경수
이성규
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LG Chem Ltd
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LG Chem Ltd
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Priority claimed from KR1020230106990A external-priority patent/KR20240031050A/ko
Application filed by LG Chem Ltd filed Critical LG Chem Ltd
Priority to JP2024525178A priority Critical patent/JP2025527380A/ja
Priority to CN202380014190.XA priority patent/CN118159513A/zh
Priority to EP23860778.2A priority patent/EP4491606A4/en
Priority to US18/707,678 priority patent/US20250197340A1/en
Publication of WO2024049101A1 publication Critical patent/WO2024049101A1/ko
Anticipated expiration legal-status Critical
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation

Definitions

  • the present invention relates to a method for producing high purity (meth)acrylic acid.
  • (meth)acrylic acid is generally produced by subjecting compounds such as propane, propylene, and (meth)acrolein to a gas phase oxidation reaction in the presence of a catalyst.
  • compounds such as propane, propylene, and (meth)acrolein
  • propane, propylene, etc. for example, in the presence of an appropriate catalyst in the reactor, propane, propylene, etc.
  • the (meth)acrylic acid-containing mixed gas is contacted with an absorption solvent such as water in an absorption tower and recovered as a (meth)acrylic acid solution.
  • an absorption solvent such as water in an absorption tower
  • subsequent processes for recovering (meth)acrylic acid contained in the (meth)acrylic acid solution generally involve processes such as extraction, distillation, and purification.
  • various methods of adjusting process conditions or process sequence have been proposed.
  • the problem to be solved by the present invention is to recover (meth)acrylic acid, which can further reduce energy usage in the purification process and simplify subsequent processes in order to solve the problems mentioned in the technology behind the invention. It is intended to provide a method.
  • contacting a mixed gas containing (meth)acrylic acid with an absorption solvent in an absorption tower first (meth)acrylic acid discharged from the bottom of the absorption tower.
  • Supplying a solution to a high boiling point by-product separation tower supplying an upper discharge stream of the high boiling point by-product separation tower to the crystallizer, and supplying a second (meth)acrylic acid solution discharged from the side of the absorption tower to the crystallizer.
  • It provides a method for producing (meth)acrylic acid, including obtaining (meth)acrylic acid crystallized in the crystallizer, and circulating the mother liquor recovered from the crystallizer to the absorption tower.
  • the method for producing (meth)acrylic acid according to the present invention can dramatically reduce energy usage, and can continuously recover high purity (meth)acrylic acid with better production efficiency compared to previous recovery methods.
  • FIG. 1 is a process flow diagram showing a method for producing (meth)acrylic acid according to an embodiment of the present invention.
  • Figure 2 is a process flow diagram showing a method for producing (meth)acrylic acid according to a comparative example.
  • the term “stream” may refer to the flow of fluid within a process, or may also refer to the fluid itself flowing within a pipe. Specifically, the stream may refer to both the fluid itself and the flow of the fluid flowing within the pipes connecting each device.
  • the fluid may mean gas or liquid, and the case where the fluid contains a solid component is not excluded.
  • contacting a mixed gas containing (meth)acrylic acid with an absorption solvent in an absorption tower supplying the first (meth)acrylic acid solution discharged from the bottom of the absorption tower to a high boiling point by-product separation tower, Supplying the top discharge stream of the high boiling point by-product separation tower to the crystallizer, supplying a second (meth)acrylic acid solution discharged from the side of the absorption tower to the crystallizer, and crystallizing
  • a method for producing (meth)acrylic acid comprising the steps of obtaining meth)acrylic acid and circulating the mother liquor recovered from the crystallizer to the absorption tower.
  • the method for producing (meth)acrylic acid may include contacting a mixed gas containing (meth)acrylic acid with an absorption solvent in the absorption tower 100.
  • the mixed gas containing (meth)acrylic acid is a general term for gaseous components discharged from the reactor 10 that produces (meth)acrylic acid through a gaseous oxidation reaction.
  • the mixed gas includes (meth)acrylic acid, unreacted raw material compounds, (meth)acrolein, inert gas, carbon monoxide, carbon dioxide, absorption solvent vapor, and various organic by-products (acetic acid, low boiling point by-products, high boiling point by-products, etc.). can do.
  • 'low boiling point by-products' (light ends) or 'high boiling point by-products' (heavies) are a type of by-product that can be produced in the production and recovery process of the desired (meth)acrylic acid, and have a molecular weight higher than (meth)acrylic acid. It can be a small or large compound.
  • the mixed gas containing (meth)acrylic acid can be prepared as follows.
  • a reaction gas containing an oxygen-containing gas and a raw material compound is supplied to a reactor 10 equipped with a catalyst through the reaction gas supply line 1, and a gas phase oxidation reaction occurs in the presence of the catalyst within the reactor 10.
  • a mixed gas containing the (meth)acrylic acid can be obtained.
  • the gas containing oxygen may be air.
  • the raw material compound may be one or more compounds selected from the group consisting of propane, propylene, butane, i-butylene, t-butylene, and (meth)acrolein. Specifically, the raw material compound may include propylene.
  • the reaction gas supplied to the reactor 10 may further include recycle gas recovered from the upper part of the absorption tower 100 and recycled. Therefore, the mixed gas containing (meth)acrylic acid may be a reaction product of a gas phase oxidation reaction of a reactant containing air, raw material compounds, and recycle gas within the reactor 10.
  • the recycle gas may originate from the top of the absorption tower 100, which will be described later. That is, the mixed gas is in contact with the absorption solvent in the absorption tower 100, and the non-condensable gas that is not dissolved in the absorption solvent may be discharged to the upper discharge stream 110 of the absorption tower 100.
  • the non-condensable gas may include impurities such as acetic acid, inert gas, unreacted raw material compounds, and a small amount of (meth)acrylic acid that is not dissolved in the absorption solvent.
  • a portion (3) of the absorption tower top discharge stream (110) may be supplied to the cooling tower (20), and the remainder (120) may be supplied to a waste gas incinerator and disposed of.
  • the content of (meth)acrylic acid in the absorption tower top discharge stream 110 may be 0.03 mol% to 0.5 mol%.
  • the cooling tower 20 is provided with an absorption solvent supply line 5 at the top, and the absorption solvent can be supplied into the cooling tower 20 from the absorption solvent supply line 5.
  • the absorption solvent may contact non-condensable gases contained in a portion 3 of the absorption tower top discharge stream 110.
  • Components contained in the non-condensable gas, such as acetic acid and (meth)acrylic acid that is not dissolved in the absorption solvent in the absorption tower 100 are dissolved in the absorption solvent, which is the lower discharge stream of the cooling tower 20. may be discharged.
  • the bottom discharge stream of the cooling tower 20 may be re-supplied to the absorption tower 100, and the bottom discharge stream of the cooling tower 20 forms a mixed stream with the separately supplied absorption solvent stream 6 for the absorption. It can be supplied to the tower 100.
  • the absorption solvent is supplied to the absorption tower 100 through the absorption solvent supply line 5 provided at the top of the cooling tower 20, and directly to the absorption tower 100 (6).
  • the absorption solvent can be supplied to the absorption tower (100) through one or more of the following supply methods, and the direct supply (6) to the absorption tower (100) forms a mixed stream with the lower discharge stream of the cooling tower (20) and is supplied to the absorption tower (100). It may be supplied to (100). Meanwhile, the supply amount of the absorption solvent supplied to the absorption tower 100 may be determined within a range in which the content of (meth)acrylic acid in the lower part of the absorption tower 100 can be maintained at 85% by weight or more.
  • the absorption solvent supplied to the cooling tower 20 and the absorption solvent supplied to the absorption tower 100 may be the same.
  • the absorption solvent may include water such as tap water or deionized water, and may include circulating process water introduced from another process (e.g., aqueous phase recycled from an extraction process and/or a distillation process).
  • the absorption solvent may contain trace amounts of organic by-products (for example, acetic acid) introduced from other processes.
  • the recycle gas can be supplied to the reactor 10 so that it can be used in a gas phase oxidation reaction for producing (meth)acrylic acid that proceeds in the reactor 10.
  • the recycle gas may be mixed with the reaction gas and supplied to the reactor 10, and may be supplied to the reactor 10 through a line separate from the line 1 through which the reaction gas is supplied.
  • acetic acid and (meth)acrylic acid in the non-condensable gas supplied from the absorption tower 100 in the cooling tower 20 may be dissolved in the absorption solvent and recycled to the absorption tower 100.
  • high-purity (meth)acrylic acid can be obtained by inducing as much of the acetic acid in the system to be discharged as possible into the upper discharge stream 110 of the absorption tower, and the loss of (meth)acrylic acid can be minimized.
  • the content of the absorption solvent in the recycle gas circulated from the cooling tower 20 to the reactor 10 can be reduced. That is, when the absorption solvent is water, by reducing the content of moisture (water) in the recycle gas, the moisture content in the stream supplied from the reactor 10 to the absorption tower 100 can be lowered, and through this, the absorption tower ( The moisture content within 100) can be lowered.
  • the absorption solvent (water) discharged from the reactor may contain dissolved various by-products that are unsuitable for introduction into the crystallizer. If the absorption solvent (water) is present in excess in the absorption tower (100), a high concentration (meth)acrylic acid solution may be dissolved. Since it is difficult to obtain, it becomes possible to introduce the side discharge stream of the absorption tower 100 directly into the crystallizer as described later by lowering the content of the absorption solvent (water) in the recycle gas.
  • the moisture content in the recycle gas may be 1% by weight to 10% by weight, specifically 3% by weight to 5% by weight.
  • the upper temperature of the cooling tower 20 for this purpose may be 35°C to 55°C, specifically 35°C to 45°C. If the upper temperature of the cooling tower 20 is lower than at least 35°C, excessive refrigerant may be consumed compared to the effect of reducing the moisture content contained in the recirculating gas, or a lower temperature refrigerant may be required, so there may not be a significant benefit from the viewpoint of efficient energy use. there is. Meanwhile, when the upper temperature of the cooling tower 20 exceeds 55°C, the content of the absorption solvent (moisture) contained in the recirculating gas transfer line 4 increases excessively, and thus the high concentration discharged from the absorption tower 100 It may be difficult to obtain a (meth)acrylic acid solution.
  • the temperature of the upper part of the cooling tower 20 is controlled by a heat exchanger provided at the bottom of the cooling tower 20, and specifically, a part of the lower stream of the cooling tower 20 is exchanged with the heat exchanger and the cooling tower 20. It can be performed by cycling. Meanwhile, the upper part of the cooling tower 20 may be operated under normal pressure operating conditions.
  • the mixed gas containing the (meth)acrylic acid is supplied to the absorption tower 100 through the reactor discharge line 2, and is contacted with the absorption solvent in the absorption tower 100 to obtain a (meth)acrylic acid solution.
  • the process can be performed. Specifically, a mixed gas containing (meth)acrylic acid, organic by-products, and absorption solvent vapor generated by the synthesis reaction of (meth)acrylic acid is brought into contact with the absorption solvent in the absorption tower 100 to produce a (meth)acrylic acid solution, specifically. First and second (meth)acrylic acid solutions can be obtained.
  • the type of the absorption tower 100 may be determined considering the contact efficiency of the mixed gas and the absorption solvent, for example, a packed column type absorption tower, a multistage tray type, etc. type) of absorption tower.
  • the packed column type absorption tower may have fillers such as rashing ring, pall ring, saddle, gauze, structured packing, etc. applied inside.
  • the mixed gas 2 may be supplied to the lower part of the absorption tower 100, and the absorption solvent, specifically the absorption solvent containing water, may be supplied to the upper part of the absorption tower 100. can be supplied.
  • the absorption tower 100 has an internal pressure of 1 to 1.5 bar or 1 to 1.3 bar, 50 to 120 °C or 50 to 100 °C, considering the condensation conditions of (meth)acrylic acid and the moisture content according to the saturated vapor pressure. Can be operated under internal temperature.
  • a first (meth)acrylic acid solution discharged from the bottom of the absorption tower 100 is obtained through an absorption process performed within the absorption tower 100, and the absorption A second (meth)acrylic acid solution discharged from the side of the tower 100 can be obtained.
  • the content of (meth)acrylic acid in the first and second (meth)acrylic acid solutions discharged from the absorption tower 100 may be 85% by weight to 99% by weight, and specifically, 85% by weight to 95% by weight. You can. This is a higher level than the content of (meth)acrylic acid in the (meth)acrylic acid solution discharged from the existing absorption tower.
  • the second (meth)acrylic acid solution can be obtained without undergoing a separate purification or separation process for the second (meth)acrylic acid solution.
  • the acrylic acid solution can be supplied directly to the crystallizer 300, thereby reducing overall process energy, and at the same time, high purity (meth)acrylic acid can be obtained from the crystallizer 300.
  • the second (meth)acrylic acid solution having such a high (meth)acrylic acid content is absorbed by, for example, optimally controlling the operating conditions of the cooling tower 20 and the absorption tower 100 according to the material components and their contents in the system. This can be achieved by minimizing the absorption solvent (moisture) content in the tower 100. That is, the absorption solvent component in the recirculating gas circulated from the cooling tower 20 to the reactor 10 is minimized, the input and usage amount of the absorption solvent supplied to the cooling tower 20 and the absorption tower 100 is minimized, and further, e.g.
  • a second (meth)acrylic acid solution having a high (meth)acrylic acid concentration can be implemented by setting the discharge number of the second (meth)acrylic acid solution discharged from the absorption tower 100.
  • the first (meth)acrylic acid solution may be discharged from the bottom of the absorption tower (100), and the second (meth)acrylic acid solution may be discharged from 80% to 99% from the top of the absorption tower (100) downward. It can be discharged from the side of the height, specifically 80% to 90% of the height.
  • the absorption solvent (moisture) in the discharged second (meth)acrylic acid solution ) and the content of high boiling point by-products can be minimized.
  • the second (meth)acrylic acid solution containing a high concentration of (meth)acrylic acid can be directly supplied to the crystallizer 300.
  • the second (meth)acrylic acid solution is discharged from a position higher than 80% downward from the top of the absorption tower 100, the content of the absorption solvent discharged through the side of the absorption tower increases.
  • the amount of (meth)acrylic acid lost to the top of the absorption tower may increase because absorption performed at a position lower than the side of the absorption tower is not sufficiently achieved.
  • the second (meth)acrylic acid solution when discharged from a position lower than the 99% point from the top of the absorption tower 100, the content of high boiling point by-products increases, so the second (meth)acrylic acid solution also The solution may become inadequate to supply to the crystallizer 300.
  • the content of (meth)acrylic acid in the second (meth)acrylic acid solution may be higher than the content of (meth)acrylic acid in the first (meth)acrylic acid solution. This is because relatively heavy high boiling point by-products are concentrated in the lowermost part of the absorption tower (100), and therefore, in the second (meth)acrylic acid solution associated with the side part of the absorption tower (100) where high boiling point by-products are almost absent (meth) )
  • the content of acrylic acid may be higher than the content of (meth)acrylic acid in the first (meth)acrylic acid solution.
  • the mixed gas is in contact with the absorption solvent in the absorption tower 100, and the non-condensable gas that is not dissolved in the absorption solvent may be discharged to the upper discharge stream 110 of the absorption tower 100.
  • a portion 3 of the overhead stream 110 may be fed to the cooling tower 20, and the remainder 120 may be fed to a waste gas incinerator for disposal.
  • the first (meth)acrylic acid solution may be supplied to the high boiling point by-product separation tower 200 along the first (meth)acrylic acid solution stream 150, and the second (meth)acrylic acid solution may be supplied to the second (meth)acrylic acid solution.
  • Acrylic acid solution may be fed to the crystallizer 300 along the stream 160.
  • the first (meth)acrylic acid solution supplied to the high boiling point by-product separation tower 200 is distilled to form a lower fraction containing high boiling point by-products, and the high boiling point by-products are removed to produce (meth)acrylic acid solution. It can be separated into an upper fraction containing a high content of acrylic acid.
  • the upper fraction of the high boiling point by-product separation tower 200 may be discharged as an upper discharge stream of the high boiling point by-product separation tower and supplied to the crystallizer 300, and the lower fraction of the high boiling point by-product separation tower 200 may be discharged as an upper discharge stream of the high boiling point by-product separation tower 200.
  • the content of meth)acrylic acid may be 85% by weight to 99% by weight, or 90% by weight to 99% by weight, or specifically 90% by weight to 95% by weight.
  • the side discharge stream 160 of the absorption tower 100 containing the second (meth)acrylic acid solution and the top discharge stream of the high boiling point by-product separation tower 200 ( 210) may be supplied to the crystallizer 300.
  • (meth)acrylic acid contained in the (meth)acrylic acid solution supplied to the crystallizer 300 can be recrystallized through a crystallization process to obtain high purity crystallized (meth)acrylic acid.
  • This crystallization process can be performed under conventional conditions.
  • the crystallization method for obtaining the product through crystallization may be a suspension crystallization or a layer crystallization method without limitation, may be continuous or batch, and may be performed in one or two or more stages.
  • the (meth)acrylic acid may be dynamically crystallized to provide high purity (meth)acrylic acid.
  • the (meth)acrylic acid solution may first flow in the form of a falling film on the inner wall of the pipe.
  • crystals can be formed on the inner wall of the tube by adjusting the temperature of the tube below the freezing point of (meth)acrylic acid. Subsequently, the temperature of the tube can be raised to near the solidification point of (meth)acrylic acid to cause sweating of about 5% by weight of (meth)acrylic acid. Then, high purity crystallized (meth)acrylic acid can be obtained by removing the perspired mother liquid from the tube and recovering the crystals formed on the inner wall of the tube.
  • the mother liquid may refer to a solution from which crystallized (meth)acrylic acid has been removed from the (meth)acrylic acid solution introduced into the crystallizer 300.
  • the mother liquid may include acetic acid, an absorption solvent, and a low boiling point substance.
  • Separation of the mother liquor and crystallized (meth)acrylic acid can be performed using a solid-liquid separation device, for example, a belt filter, a centrifuge, etc.
  • the mother liquid may be discharged from the crystallizer and circulated to the absorption tower 100 along the mother liquid circulation line 310.
  • the mother liquid can be directly supplied to the absorption tower 100 without going through a separate purification process or separation process. That is, the ratio of the flow rate when the mother liquor recovered from the crystallizer 300 is introduced into the absorption tower to the flow rate when the mother liquor is discharged from the crystallizer may be 0.99 to 1.01, and more specifically, the The flow rate ratio may be 1. Meanwhile, the process is simplified by not performing a separate process for the mother liquor, such as a distillation process, and energy costs can be greatly reduced because the absorption solvent contained in the mother liquor, specifically water, does not need to be distilled.
  • the composition is (meth)acrylic acid (7.0 mol%) and water.
  • a mixed gas (2) containing (11.8 mol%), high boiling point material (0.09 mol%), and inert gas (80.6 mol%) was obtained.
  • the mixed gas (2) was introduced into the 22nd stage from the top of the absorption tower (100) at a temperature of 164°C.
  • the pressure at the top of the absorption tower (100) is 1.1 bar and the temperature at the bottom of the absorption tower (100) is 96.4°C, and the absorption solvent (water) introduced into the absorption tower (100) is a stream (6) supplied directly to the absorption tower. and fed through the bottom discharge stream of the cooling tower (20).
  • the absorption solvent was introduced into the upper part of the absorption tower (100) at a flow rate of 6.6% by weight compared to the flow rate of the mixed gas (2).
  • the mother liquid 310 circulated from the crystallizer described later was introduced into the 15th stage from the top of the absorption tower 100 at a mass flow rate of 1.3 times the flow rate of the absorption solvent introduced into the absorption tower 100.
  • the ratio of the mass flow rate when the recovered mother liquor was introduced into the absorption tower 100 to the flow rate when the mother liquor recovered from the crystallizer 300 was discharged from the crystallizer 300 was 1.
  • an absorption tower top discharge stream 110 containing non-condensable gas, a first (meth)acrylic acid solution stream 150 containing a first (meth)acrylic acid solution, and A second (meth)acrylic acid solution stream 160 containing a second (meth)acrylic acid solution was obtained.
  • the content of (meth)acrylic acid contained in the absorption tower top discharge stream 110 was 0.146 mol%.
  • a portion (3) of the absorption tower top discharge stream was supplied to the cooling tower (20), and the remainder (120) was disposed of outside the system.
  • the cooling tower (20) the non-condensable gas contained in the portion (3) of the absorption tower upper discharge stream and the absorption solvent supplied from the absorption solvent supply line (5) contact, and the absorption solvent and the absorption solvent dissolved in the absorption solvent are contacted.
  • a portion of the bottom discharge stream of the cooling tower (20) was fed to the absorption tower (100), and the remainder was circulated to the cooling tower (20). At this time, the moisture content in the recycle gas 4 was 4.4% by weight.
  • the first (meth)acrylic acid solution 150 discharged from the bottom of the absorption tower 100 contains (meth)acrylic acid (85.9% by weight), acetic acid (1.3% by weight), water (4.2% by weight), and furfural. (3.2% by weight), maleic acid (5.0% by weight), and the second (meth)acrylic acid solution (160) discharged from the side at a height of 86% from the top of the absorption tower contains (meth)acrylic acid (88.8% by weight) %), acetic acid (2.3% by weight), water (5.3% by weight), furfural (3.1% by weight), and maleic acid (0.06% by weight).
  • the second (meth)acrylic acid solution stream 160 was obtained at a mass flow rate of 7.3 times the mass flow rate of the first (meth)acrylic acid solution stream 150.
  • the mass flow rate of the absorption solvent contained in the first and second (meth)acrylic acid solutions was 30% by weight compared to the flow rate of the absorption solvent introduced into the absorption tower 100.
  • the first (meth)acrylic acid solution stream 150 is supplied to the high boiling point by-product separation tower 200, the high boiling point by-product is separated through the lower discharge stream 220 of the high boiling point by-product separation tower, and (meth)acrylic acid is produced.
  • the top discharge stream 210 of the high boiling point by-product separation tower was formed into a mixed stream with the second (meth)acrylic acid solution stream 160, and then supplied to the crystallizer 300.
  • the content of (meth)acrylic acid in the top discharge stream 210 of the high boiling point by-product separation tower was 92.8% by weight.
  • the mixed stream of the top discharge stream 210 of the high boiling point by-product separation tower and the second (meth)acrylic acid solution stream 160 contains high boiling point by-products furfural (2.8% by weight) and maleic acid (0.06% by weight). included.
  • a mixed stream of the top discharge stream 210 of the high boiling point by-product separation tower and the second (meth)acrylic acid solution stream 160 is crystallized to contain (meth)acrylic acid.
  • (meth)acrylic acid was finally obtained from the recovery stream (320), and the mother liquor was supplied to the absorption tower (100) through the mother liquor circulation line (310).
  • the content of (meth)acrylic acid contained in the (meth)acrylic acid recovery stream 320 was 99.5% by weight or more.
  • Example 2 was (meth)acrylic acid in the same process flow as Example 1, except that the second (meth)acrylic acid solution discharged from a height of 77% downward from the top of the absorption tower 100 was supplied to the crystallizer. was manufactured.
  • the second (meth)acrylic acid solution contains (meth)acrylic acid (88.8% by weight), acetic acid (2.2% by weight), water (5.4% by weight), furfural (3.2% by weight), and maleic acid (0.04% by weight). ) was included.
  • the content of (meth)acrylic acid in the (meth)acrylic acid recovery stream 320 was more than 99.5% by weight, and through this, (meth)acrylic acid was obtained. Meanwhile, the content of (meth)acrylic acid contained in the absorption tower top discharge stream 110 was 0.25 mol%.
  • the (meth)acrylic acid solution was not obtained from the side and bottom of the absorption tower (100), but the (meth)acrylic acid solution was obtained only from the bottom of the absorption tower, and this was input into the crystallizer (300).
  • (meth)acrylic acid (320) was obtained.
  • the mother liquid 310 after crystallization is input into the high boiling point by-product separation tower 200, and the discharge stream 220 from the bottom of the high boiling point by-product separation tower containing high boiling point by-products and the mother liquid from which the high boiling point by-products have been removed are produced.
  • a by-product separation tower overhead stream (210) was obtained.
  • the high boiling point by-product separation tower top discharge stream (210) was recycled to the absorption tower (100). Except for this, (meth)acrylic acid was prepared in the same manner as in Example 1.
  • the (meth)acrylic acid solution contained (meth)acrylic acid (90.5% by weight), acetic acid (1.8% by weight), water (5.9% by weight), furfural (0.7% by weight), and maleic acid (0.7% by weight). . This was put into the crystallizer 300, and it was confirmed that the content of (meth)acrylic acid in the (meth)acrylic acid recovery stream 320 was more than 99.5% by weight.
  • the energy used to remove high-boiling by-products in the high-boiling by-product separation tower (200) was 154.5 kcal/kg AA, which is about 4 of the energy used in the high-boiling by-product separation tower (200) in Example 1. You can see that more than twice as much energy has been consumed. Meanwhile, the content of (meth)acrylic acid (loss of acrylic acid) contained in the absorption tower top discharge stream 110 was 0.144 mol%.

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  • Organic Chemistry (AREA)
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PCT/KR2023/012550 2022-08-30 2023-08-24 고순도 (메트)아크릴산의 제조방법 Ceased WO2024049101A1 (ko)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2024525178A JP2025527380A (ja) 2022-08-30 2023-08-24 高純度（メタ）アクリル酸の製造方法
CN202380014190.XA CN118159513A (zh) 2022-08-30 2023-08-24 制备高纯度(甲基)丙烯酸的方法
EP23860778.2A EP4491606A4 (en) 2022-08-30 2023-08-24 PROCESS FOR PREPARING HIGH-PURITY (METH)ACRYLIC ACID
US18/707,678 US20250197340A1 (en) 2022-08-30 2023-08-24 Method for preparation of high-purity (meth)acrylic acid

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
KR20220109412 2022-08-30
KR10-2022-0109412 2022-08-30
KR1020230106990A KR20240031050A (ko) 2022-08-30 2023-08-16 고순도 아크릴산의 제조방법
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KR20120103520A (ko) * 2011-03-11 2012-09-19 주식회사 엘지화학 (메트)아크릴산의 연속 회수 방법 및 회수 장치
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