US20090088579A1 - Production Method of N-Vinyl-2-Pyrrolidone - Google Patents

Production Method of N-Vinyl-2-Pyrrolidone Download PDF

Info

Publication number
US20090088579A1
US20090088579A1 US11/918,228 US91822806A US2009088579A1 US 20090088579 A1 US20090088579 A1 US 20090088579A1 US 91822806 A US91822806 A US 91822806A US 2009088579 A1 US2009088579 A1 US 2009088579A1
Authority
US
United States
Prior art keywords
nvp
crystallization
crystallizer
crystallization process
mother liquor
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.)
Abandoned
Application number
US11/918,228
Other languages
English (en)
Inventor
Hideto Sugiura
Toru Inaoka
Shigeyuki Nozaki
Yoshihisa Oka
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.)
Nippon Shokubai Co Ltd
Original Assignee
Nippon Shokubai 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 Nippon Shokubai Co Ltd filed Critical Nippon Shokubai Co Ltd
Assigned to NIPPON SHOKUBAI CO., LTD. reassignment NIPPON SHOKUBAI CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SUGIURA, HIDETO, INAOKA, TORU, OKA, YOSHIHISA, NOZAKI, SHIGEYUKI
Publication of US20090088579A1 publication Critical patent/US20090088579A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/267—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atom
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D9/00—Crystallisation
    • B01D9/0059—General arrangements of crystallisation plant, e.g. flow sheets
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
    • C07D201/16—Separation or purification

Definitions

  • the present invention relates to a stable production method of high-purity N-vinyl-2-pyrrolidone.
  • NVP N-vinyl-2-pyrrolidone
  • polymers of NVP are used extensively in various fields such as pharmaceuticals, cosmetics, adhesives, paints, dispersants, inks, electronic parts and photoresist materials because of their advantages such as biocompatibility, stability and hydrophilicity.
  • Impurities are firmly required to be removed in these fields. Therefore, it is proposed to control the concentration of impurities in a mother liquor at a constant level in search of a method for obtaining high-purity NVP (JP-A-2004-345994).
  • JP-A-2004-345993 A method for obtaining NVP of extremely high purity while improving energy efficiency by reducing stages in a crystallization process is proposed (JP-A-2004-345993).
  • the purity of NVP to be supplied to the first crystallization process is generally low, resulting in low purity of the obtained NVP and a high load of a crystal purification process, because a mother liquor from the first crystallization process is recycled for use to the first crystallization process. Further, much time is necessary in a purification process to obtain high-purity NVP, which sometimes results in low production efficiency.
  • the present invention can provide a production method of NVP characterized by comprising at least two crystallization processes, supplying the mother liquor from the first crystallization process to second crystallization process and supplying, as needed, the crystals from the crystallization processes to a crystal purification process where a sweating phenomenon is applied.
  • JP-A-2004-345994 discloses that it is preferable to control the concentration of impurities in a crude NVP solution at a constant level at the inlet of a crystallizer to prevent quality degradation of obtained NVP, but does not give any detail information on controlling the concentration of impurities.
  • high-purity NVP can be stably produced without plugging in a crystallizer caused by crystals that could deposit on the heat transfer surface by controlling the water content in a feed NVP solution within a specific range.
  • FIG. 1 is an illustration showing a method for purifying NVP in crystallization.
  • FIG. 2 is an illustration showing another method for purifying NVP in crystallization.
  • FIG. 3 is an illustration showing the other method for purifying NVP in crystallization.
  • FIG. 4 is an illustration showing still the other method for purifying NVP in crystallization.
  • a production method of NVP can be provided, characterized by comprising at least two crystallization processes, supplying the mother liquor from the first crystallization process to the second crystallization process and supplying, as needed, the crystals from the crystallization process to a crystal purification process where a sweating phenomenon is applied.
  • FIG. 1 is an illustration showing a method for purifying NVP in crystallization.
  • purification of NVP is carried out in a combination of two crystallizers 12 , 13 and crystal purification apparatus 14 .
  • the first crystallization process is supplied with only distilled NVP 11
  • the second crystallization process is supplied with a recovered mother liquor.
  • Distilled NVP is used as feed NVP to the first crystallization process using crystallizer 12 , whereas a mother liquor from the first crystallization process and a mother liquor from the second crystallization process and, as needed, a mother liquor and a sweating solution from the crystal purification process using crystal purification apparatus 14 are mixed and controlled for water content thereof to obtain a feed solution to the second crystallization process using crystallizer 13 .
  • the feed NVP is crystallized in the first crystallization process and the crude crystals obtained by filtration are purified in the crystal purification process to obtain product 15 .
  • the crude crystals obtained from the second crystallization process are sent to the crystal purification process and purified in the same way to obtain product 15 .
  • Distilled NVP provides crystals of higher purity because it contains less amount of impurities compared with a recovered mother liquor. Therefore, the crystals to be supplied to a crystal purification process of which the purity is higher than that of the crystals obtained from the recovered mother liquor improve the purity of the product NVP. Further, this leads to an increase of the amount of production due to a lighter load in the crystal purification process.
  • the concentration of impurities in the mother liquor is controlled so as to be generally not higher than 10%, preferably not higher than 6%.
  • the first crystallization process, the second crystallization process and the crystal purification process in the first embodiment can be operated continuously. Each process may be operated independently, but preferably operated continuously in view of production efficiency.
  • Feed NVP to be supplied in the first embodiment includes crude NVP synthesized by various methods such as crude NVP obtained by vinylating 2-pirrolidone with acetylene; crude NVP obtained as a dehydrated salt by reacting butyrolactone with ethanolamine and then replacing a hydroxyl group of thus obtained 1-( ⁇ -oxyethyl)-2-pirrolidone with chlorine using thionyl chloride; crude NVP obtained by removing an acetic acid from an acetic ester intermediate produced by reacting N-(2-hydroxyethyl)-2-pirrolidone with acetic anhydride; and crude NVP obtained by gas-phase intramolecular dehydration (sometimes abbreviated as “gas-phase dehydration”) of N-hydroxyethyl-2-pirrolidone in the presence of a catalyst.
  • gas-phase dehydration gas-phase intramolecular dehydration
  • the melting point of NVP is 13.5° C.
  • Crude NVP that contains few impurities may be used directly as a raw material for crystallization, but when it contains many impurities, it is used as a raw material for crystallization after purified by a known method such as fractional distillation.
  • the impurities include water, 2-pirrolidone that is a decomposition product of N-hydroxyethyl-2-pirrolidone, N-hydroxyethyl-2-pirrolidone that is an unreacted raw material, and a polymer.
  • distilled NVP can be used as a raw material for crystallization. Because impurities removed by distillation and impurities removed by crystallization are not always the same, the combination of both methods is effective for improving purity.
  • the purity of NVP is not particularly restricted, but it is preferably within the range between about 97% and about 99%. Even when NVP has a purity of over 99.95%, it can be used as a raw material without any problem if its purity is lower than that of the product NVP.
  • NVP can be distilled by a known method. For example, see JP-A-2004-345994.
  • a NVP-containing solution recovered from a crystallization process, a filtration process, a crystal purification process and the like may be used as a part of raw material for crystallization.
  • the mixing thereof is carried out using a known agitator.
  • the mixing ratio with distillated NVP is adjusted as appropriate without particular restriction.
  • a crystallization apparatus includes, for example, a continuous crystallizer such as a forced-circulation type crystallizer, a multistage crystallizer, a conveying layer type crystallizer, a classified-product-removal crystallizer, a turbulent type mixed- and classified-product-removal crystallizer, a double crystallizer, a direct-contact-refrigeration crystallizer and a flocculate formation technology; and a cooling type crystallizer such as a tank type crystallizer, a Swenson-Walker crystallizer, a Howard crystallizer and a drum flaker.
  • a continuous crystallizer such as a forced-circulation type crystallizer, a multistage crystallizer, a conveying layer type crystallizer, a classified-product-removal crystallizer, a turbulent type mixed- and classified-product-removal crystallizer, a double crystallizer, a direct-contact-refrigeration crystallizer and a flocculate formation technology
  • a feed NVP solution is crystallized in the above crystallizers making use of a cooling medium such as water and an aqueous solution of ethylene glycol. Crystallization is preferably carried out continuously by controlling the temperature (for example, ⁇ 20° C. to 13.5° C.) of the mother liquor discharged from the outlet so that the concentration of the slurry (mother liquor containing depositing crystals) in the mother liquor is a specified concentration, for example, 5 to 60%, and adjusting a retention time.
  • the above mother liquor (feed NVP in a crystallizer) can be recycled to the crystallization process.
  • a stabilizer may be added to a feed NVP solution and a mother liquor.
  • the stabilizer is not restricted so long as it can inhibit NVP polymerization, and includes, for example, a phenol-based antioxidant and an amine-based polymerization inhibitor. These stabilizers may be used alone or in combination.
  • N,N′-di-sec-butyl-p-phenylenediamine, p-phenylenediamine, N,N′-diethyl-p-phenylenediamine, N,N′-diphenyl-p-phenylenediamine or 2,6-t-butyl-4-hydroxytoluene are preferable in view of inhibiting ability against NVP polymerization.
  • the amount of a stabilizer to be used is not particularly restricted so long as NVP polymerization is inhibited or reduced.
  • a stabilizer is present in the concentration range of generally not higher than 1.5% by weight (not including 0%), preferably 0.1 ppm to 1.0% by weight based on the weight of NVP.
  • a stabilizer may be directly added to a feed NVP solution or a mother liquor at the inlet of a crystallizer.
  • a specific amount of a stabilizer dissolved or dispersed in feed NVP or a stabilizer present in a crystallization process can inhibit or reduce NVP polymerization and thus can prevent liquid or slurry viscosity from increasing.
  • the slurry discharged from the outlet may be transferred to a subsequent filtration process or further to a crystal purification process.
  • the mother liquor to be recovered may be subjected to an additional purification method that specifically includes distillation, filtration, centrifugal separation, adsorption and extraction purification.
  • Distillation purification includes simple distillation, continuous multistage distillation and batch multistage distillation.
  • Filtration purification includes pressure filtration, vacuum filtration and gravity filtration.
  • Centrifugal separation purification includes decantation and centrifugal filtration.
  • Adsorption purification includes fixed-bed adsorption using an adsorbent such as activated carbon, silica gel, alumina and a molecular sieve, moving-bed adsorption, fluidized-bed adsorption and agitated-tank adsorption.
  • Extraction purification includes batch extraction, multiple extraction, semibatch extraction and multistage extraction.
  • a filtration process is not particularly restricted so long as an obtained crystal phase and a liquid residue phase can be separated.
  • a known continuous or batch filtration method is generally used.
  • a crystal purification (or rectification) process is not restricted and is preferably used when higher-purity of NVP is required.
  • Crystal purification is not particularly restricted, but preferably uses a method that makes use of sweating. Sweating is a method for crystal purification wherein a relatively impure part of crystals is melted away by melting a part of the crystals to purify the crystals, and it is not limited especially.
  • a tower type purification apparatus KCP made by Kureha Engineering Co. Ltd.
  • MVB falling liquid film type apparatus
  • the crystals from the first crystallization process and the second crystallization process are preferably transferred in a crystal form without melting in view of energy efficiency.
  • the liquid containing impurities generated in these processes can be used after mixed with mother liquors from the second and subsequent crystallization process.
  • the method based on the second embodiment of the present invention is a method for stably producing high-purity NVP and characterized by controlling the water content in a feed NVP solution at the inlet of a crystallizer within a specific range.
  • the above method includes a method having at least one crystallization process where a multistage fractional crystallization process or single or plural dynamic or static crystallization stages are included, and a method where crystal purification is carried out after crystallization.
  • the water content needs to be adjusted at least at the inlet of the first crystallization process, but may be controlled or may not be controlled in the second and subsequent crystallization process depending on circumstances.
  • the object material of attention in the second embodiment is water.
  • the water content in a feed NVP solution at the inlet of a crystallizer is preferably not lower than 0.7% by weight and not higher than 10% by weight, more preferably not lower than 0.8% by weight and not higher than 7% by weight and particularly most preferably not lower than 1% by weight and not higher than 5% by weight.
  • the water content at the inlet of a crystallizer should be controlled so as to be within the above range.
  • the method for controlling the water content is not particularly restricted and includes a method where the water content in crude NVP introduced in an adjusting tank is measured and controlled by adding crude NVP or water based on the measurement, and a method where the water content in crude NVP is measured and controlled by adding crude NVP or water using a device such as a static mixer installed in a pipeline before the inlet of a crystallizer.
  • the pH value of a feed NVP solution at the inlet of a crystallizer is preferably not lower than 6.0 and not higher than 13.0, more preferably not lower than 6.5 and not higher than 12.5 and particularly most preferably not lower than 7.0 and not higher than 12.0.
  • pH value is not within the above range, production rate of NVP is reduced, which is not preferable from the industrial and economical standpoints.
  • the temperature of a feed NVP solution at the inlet of a crystallizer is not particularly restricted so long as the solution does not freeze, and is preferably not lower than 7.0° C. and not higher than 30.0° C., more preferably not lower than 9.0° C. and not higher than 25.0° C. and particularly most preferably not lower than 11.0° C. and not higher than 20.0° C.
  • the temperature is preferably within the above range.
  • thermometer bulb one minute after the thermometer is set.
  • a thermocouple can be used depending on circumstances.
  • the second embodiment can be applied to the method shown in FIG. 1 described in the first embodiment.
  • at least two crystallizers are used and distilled NVP is supplied to the first crystallization process, whereas the mixture of NVP recovered from the first crystallization process and NVP recovered from the second crystallization process is supplied to the second crystallization process after the water content thereof is adjusted.
  • FIG. 2 is an illustration showing another method for purifying NVP in crystallization.
  • Purification of NVP is carried out using crystallizer 22 in FIG. 2 .
  • One crystallizer is used, and distilled NVP and NVP recovered from a crystallization process are mixed and then the water content of the mixture is adjusted.
  • feed NVP is obtained by mixing distilled NVP 21 and the mother liquor recovered from the crystallization process and then adjusting the water content of the mixed liquid.
  • Feed NVP is purified using crystallizer 22 and then filtered to obtain crystals as product 25 .
  • the concentration of impurities in a mother liquor is controlled so as to be generally not higher than 10%, preferably not higher than 6%.
  • FIG. 3 is the same in this respect.
  • FIG. 3 is an illustration showing the other method for purifying NVP in crystallization.
  • crystallizer 32 and crystal purification apparatus 34 are combined to carry out NVP purification.
  • NVP of higher purity is obtained by combining a crystallizer with a crystal purification apparatus than that obtained in the case of a crystallizer alone.
  • feed NVP is obtained by mixing distilled NVP 31 , the mother liquor recovered from the crystallization process using crystallizer 32 and, as needed, the mother liquor and sweating solution recovered from a crystal purification process using crystal purification apparatus 34 and then adjusting the water content in the mixed liquid.
  • Feed NVP is treated in crystallizer 32 and filtered to obtain crude crystals, which are then purified in crystal purification apparatus 34 to obtain product 35 .
  • a part of a mother liquor and sweating solution recovered from a crystal purification process is taken out of the system to adjust the concentration of impurities in this method.
  • FIG. 4 is an illustration showing still the other method for purifying NVP in crystallization.
  • Distilled NVP 41 is crystallized in a crystallization process using crystallizer 42 to obtain crystals as product 45 .
  • Feed NVP to be supplied to a crystallization process was obtained by gas-phase dehydration of N-hydroxyethyl-2-pirrolidone followed by purification by distillation.
  • the obtained crude NVP had a purity of 97.3125% and an organic-impurity concentration of 21,600 ppm.
  • the organic impurities include 2-pirrolidone which is a decomposition product of N-hydroxyethyl-2-pirrolidone, N-hydroxyethyl-2-pirrolidone which is an unreacted raw material, polymers and the like.
  • Feed NVP to be supplied to a crystallization process was obtained by gas-phase dehydration of N-hydroxyethyl-2-pirrolidone followed by purification by distillation.
  • the purity and the water content of the distilled NVP were in the range of 98.85% to 98.40% and in the range of 0.02% to 0.03% respectively.
  • NVP concentration, water content and pH of feed NVP and NVP in examples were measured by gas chromatography, Karl Fischer Method and a pH meter respectively.
  • NVP concentration (sometimes referred to as purity) is measured using gas chromatography (column: DB-1 made by SPELCO, carrier gas: He, flow rate: 17.2 mL/min, temperature: 60° C. to 250° C.).
  • Water content is measured using a Karl Fischer meter (DL18 model made by METTLER, solvent: methanol).
  • Crude NVP was supplied continuously to horizontal multistage cooling crystallizer 1 (the first crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the above crystallizer was operated under the conditions of a feed rate of the crude NVP solution to above crystallizer 1 of 75 kg/h, a feed temperature of 6.5° C. and a retention time of 4 hours.
  • the obtained slurry was filtered with a belt-type filter.
  • the obtained NVP crystals had a purity of 99.1975% and an organic-impurity concentration of 5,150 ppm.
  • the rate of NVP crystal generation was 15 kg/h.
  • the crystals obtained by filtration were mixed with the crystals from the second crystallization process to be described later and then supplied continuously to a tower type purification apparatus at a feed rate of 50 kg/h.
  • Ultrapure NVP was obtained at a rate of 35 kg/h under the conditions of a retention time of 0.5 hours and heating at the top of the tower with hot water of 30° C. to 50° C.
  • Analysis of the obtained NVP showed a purity of 99.9920% and an organic-impurity concentration of 50 ppm.
  • the mother liquor after filtration with a belt-type filter from the first crystallization process was mixed with the mother liquor from the second crystallization process and then supplied continuously to another horizontal multistage cooling crystallizer 2 (the second crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the above crystallizer was operated under the conditions of a flow rate of the mother liquor to crystallizer 2 of 85 kg/h, a feed temperature of 6.5° C. and a retention time of 2.5 hours.
  • the obtained NVP crystals had a purity of 98.9930% and an organic-impurity concentration of 7,700 ppm.
  • the rate of NVP crystallization was 35 kg/h.
  • the mother liquor obtained by filtrating the slurry from above crystallizer 2 with a belt-type filter was sent back to above crystallizer 2 at a rate of 25 kg/h.
  • Crude NVP was supplied continuously to a drum flaker (the first crystallization process) to obtain NVP crystals and a mother liquor.
  • the drum flaker was operated under the conditions of a feed rate of the crude NVP solution to the drum flaker of 75 kg/h, a feed temperature of 6.5° C., a drum surface area of 2 m 2 and a retention time of 2 hours.
  • the obtained NVP crystals had a purity of 99.0995% and an organic-impurity concentration of 6,300 ppm.
  • the rate of NVP crystallization was 7.5 kg/h.
  • the above crystals were mixed with the crystals from the second crystallization process to be described later and then supplied continuously to a tower type purification apparatus at a feed rate of 50 kg/h.
  • Ultrapure NVP was obtained at a rate of 35 kg/h under the conditions of a retention time of 0.5 hours and heating at the top of the tower with hot water of 30° C. to 50° C.
  • Analysis of the obtained NVP showed a purity of 99.9910% and an organic-impurity concentration of 50 ppm.
  • the mother liquor from the drum flaker was mixed with the mother liquor sent back from the second crystallization process and then supplied continuously to a horizontal multistage cooling crystallizer (the second crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the above crystallizer was operated under the conditions of a feed rate of the mother liquor to the crystallizer of 102 kg/h, a feed temperature of 6.5° C. and a retention time of 3 hours.
  • the obtained NVP crystals had a purity of 98.9475% and an organic-impurity concentration of 8,400 ppm.
  • the rate of NVP crystallization was 42.5 kg/h.
  • the mother liquor obtained by filtrating the slurry from above crystallizer 2 with a belt-type filter was sent back to above crystallizer 2 at a rate of 35 kg/h.
  • Crude NVP was supplied continuously to horizontal multistage cooling crystallizer 1 (the first crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the above crystallizer was operated under the conditions of a feed rate of the crude NVP solution to above crystallizer 1 of 75 kg/h, a feed temperature of 6.5° C. and a retention time of 4 hours.
  • the obtained slurry was filtered with a belt-type filter.
  • the obtained NVP crystals had a purity of 98.9995% and an organic-impurity concentration of 6,500 ppm.
  • the rate of NVP crystallization was 15 kg/h.
  • the mother liquor after filtration with a belt-type filter was mixed with the mother liquor sent back from the second crystallization process and then supplied continuously to horizontal multistage cooling crystallizer 2 (the second crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the above crystallizer was operated under the conditions of a feed rate of the mother liquor to the crystallizer of 85 kg/h, a feed temperature of 6.5° C. and a retention time of 2 hours.
  • the obtained NVP crystals had a purity of 98.9040% and an organic-impurity concentration of 7,500 ppm.
  • the rate of NVP crystallization was 35 kg/h.
  • the mother liquor after filtration was sent back to the second crystallization process at a rate of 25 kg/h, whereas the crystals after filtration were supplied to a tower type purification apparatus at a rate of 35 kg/h.
  • Ultrapure NVP was obtained at a rate of 25 kg/h under the conditions of a retention time of 0.5 hours and heating at the top of the tower with hot water of 30° C. to 50° C. Analysis of the obtained NVP showed a purity of 99.9885% and an organic-impurity concentration of 70 ppm.
  • Crude NVP was supplied continuously to a tank type crystallizer (the first crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the tank type crystallizer was operated under the conditions of a feed rate of the crude NVP solution to the crystallizer of 75 kg/h, a feed temperature of 6.5° C. and a retention time of 4 hours.
  • the obtained slurry was then separated into crystals and a mother liquor with a centrifugal separator.
  • the obtained NVP crystals had a purity of 99.1755% and an organic-impurity concentration of 5,500 ppm.
  • the rate of NVP crystallization was 15 kg/h.
  • the separated mother liquor was mixed with the mother liquor sent back from the second crystallization process and then supplied continuously to a horizontal multistage cooling crystallizer (the second crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the crystallizer was operated under the conditions of a feed rate of the mother liquor to the crystallizer of 85 kg/h, a feed temperature of 6.5° C. and a retention time of 2 hours.
  • the obtained NVP crystals had a purity of 98.194% and an organic-impurity concentration of 7,500 ppm.
  • the rate of NVP crystallization was 35 kg/h.
  • the mother liquor obtained by filtrating the slurry from the second crystallization process with a belt-type filter was sent back to the second crystallization process at a rate of 25 kg/h.
  • the crystals after filtration were mixed with the crystals from the first crystallization process and then supplied continuously to a tower type purification apparatus at a rate of 50 kg/h.
  • Ultrapure NVP was obtained at a rate of 35 kg/h under the conditions of a retention time of 0.5 hours and heating at the top of the tower with hot water of 30° C. to 50° C.
  • Analysis of the obtained NVP crystals showed a purity of 99.9765% and an organic-impurity concentration of 70 ppm.
  • Crude NVP was supplied continuously to a horizontal multistage cooling crystallizer (the first crystallization process) to obtain a slurry containing NVP crystals and a mother liquor.
  • the feed rate of the mother liquor to the above crystallizer was 75 kg/h, which consisted of 10 kg/h of virgin crude NVP and 65 kg/h of the recovered mother liquor from the first crystallization process.
  • This mixed liquid was supplied at a temperature of 6.5° C. and a retention time of 4 hours.
  • the rate of NVP crystallization was 15 kg/h.
  • the above slurry was then taken out of the first crystallization process and filtered with a belt-type filter.
  • the obtained NVP had a purity of 97.3985% and an organic-impurity concentration of 15,450 ppm.
  • the crystals after filtration was supplied continuously to a tower type purification apparatus at a retention time of 1 hour to obtain high-purity NVP at a rate of 10.5 kg/h.
  • the NVP had a purity of 98.6795% and an organic-impurity concentration of 8,350 ppm.
  • Crude NVP was supplied continuously to each crystallization process to obtain a slurry containing NVP crystals and a mother liquor.
  • the feed rate of the mother liquor to each crystallization process was 37.5 kg/h, which consisted of 5 kg/h of virgin crude NVP and 32.5 kg/h of the recovered mother liquor from each crystallization process.
  • This mixed liquid was supplied at a temperature of 6.5° C. and a retention time of 6 hours.
  • the rate of NVP crystallization was 15 kg/h in each process.
  • the above slurry was then taken out of each crystallization process and filtered with a belt-type filter.
  • the NVP obtained from the first crystallization process had a purity of 97.1825% and an organic-impurity concentration of 16,850 ppm, whereas the NVP obtained from the second crystallization process had a 97.2225% and an organic-impurity concentration of 16,550 ppm.
  • the crystals from each crystallization process were mixed after filtration and supplied continuously to a tower type purification apparatus at a retention time of 1 hour to obtain NVP at a rate of 10.5 kg/h.
  • the NVP had a purity of 98.3465% and an organic-impurity concentration of 9,650 ppm.
  • the NVP obtained from the first crystallization process of each example had generally higher purity than that obtained from the first crystallization process of each comparative example.
  • the NVP obtained from the second crystallization process of each example had higher purity than that obtained from the second crystallization process of Comparative Example 2. Therefore, the effect of the present invention that high-purity NVP could be obtained by supplying the mother liquor from the first crystallization process to the second crystallization process was demonstrated.
  • NVP of higher purity from each crystallization process improved efficiency of a purification process where a sweating phenomenon was applied.
  • Table I-1 it can be understood that NVP of higher purity is obtained in each example than in each comparative example at a rate of crystallization as high or twice as high as that in each comparative example even though the retention time in each example is only half of that in each comparative example.
  • High-purity NVP can be efficiently produced by supplying the mother liquor from the first crystallization process to the second crystallization process.
  • NVP NVP was purified according to the method shown in FIG. 4 .
  • NVP Distilled NVP of a water content of 0.02% by weight and a purity of 98.80% was added with water to obtain feed NVP (pH: 11.0, temperature: 11.3° C.) of a water content of 1.18% by weight, which was supplied continuously at a feed rate of 75 kg/h to a horizontal multistage cooling crystallizer and crystallized for purification at 6.5° C. and a retention time of 4 hours for 7 days in series. It turned out that NVP of a purity of not lower than 99.98% was stably obtained in a continuous operation without depositing of crystals on the heat transfer surface of the crystallizer that may cause a shutdown of the crystallizer.
  • NVP NVP was purified according to the method shown in FIG. 2 .
  • Crystallization was carried out in the same way as Example II-1 except that distilled NVP of a water content of 0.02% by weight and a purity of 99.12% was mixed with the NVP of a water content of 2.20% by weight and a purity of 98.54% recovered from a crystallizer at a mixing ratio of 4:6 by weight and then added with water to obtain feed NVP (pH: 11.3, temperature: 13.2° C.) of a water content of 3.57% by weight. It turned out that NVP of a purity of not lower than 99.97% was stably obtained in a continuous operation without depositing of crystals on the heat transfer surface of the crystallizer that may cause a shutdown of the crystallizer.
  • NVP NVP was purified according to the method shown in FIG. 2 .
  • Crystallization was carried out in the same way as Example II-1 except that distilled NVP of a water content of 0.03% by weight and a purity of 99.24% was mixed with the NVP of a water content of 1.80% by weight and a purity of 98.33% recovered from a crystallization mother liquor at a mixing ratio of 4:6 by weight and then added with water to obtain feed NVP (pH: 11.0, temperature: 10.1° C.) of a water content of 8.89% by weight.
  • the crystallization mother liquor was taken out of the system at a rate of 2 L/h to prevent quality deterioration of the NVP, whereas water was added to the system at a rate of 0.2 L/h to keep the water content constant. It turned out that NVP of a purity of not lower than 99.95% was stably obtained in a continuous operation without depositing of crystals on the heat transfer surface of the crystallizer that may cause a shutdown of the crystallizer.
  • NVP NVP was purified according to the method shown in FIG. 3 .
  • Distilled NVP of a water content of 0.03% by weight and a purity of 98.99% was mixed with the NVP of a water content of 1.15% by weight and a purity of 98.08% recovered from a crystallization mother liquor at a mixing ratio of 4:6 by weight and then added with water to obtain feed NVP (pH: 10.8, temperature: 12.2° C.) of a water content of 0.91% by weight, which was supplied continuously at a feed rate of 75 kg/h to a horizontal multistage cooling crystallizer and crystallized for purification at a temperature of 6.5° C. and a retention time of 4 hours for 7 days in series.
  • the crystallization mother liquor was taken out of the system at a rate of 4 L/h to prevent quality deterioration of the NVP, whereas water of 0.4 L was added to the system every 8 hours to keep the water content constant. It turned out that NVP of a purity of not lower than 99.95% was stably obtained in a continuous operation without depositing of crystals on the heat transfer surface of the crystallizer that may cause a shutdown of the crystallizer.
  • the obtained NVP was supplied to a tower type purification apparatus where a sweating phenomenon was applied and subjected to further purification there to obtain NVP of a purity of not lower than 99.99%.
  • NVP NVP was purified according to the method shown in FIG. 2 .
  • Crystallization was carried out in the same way as Example II-1 except that distilled NVP of a water content of 0.02% by weight and a purity of 97.87% was mixed with the NVP of a water content of 0.56% by weight and a purity of 98.33% recovered from a crystallization mother liquor at a mixing ratio of 4:6 by weight to obtain the feed NVP (pH: 10.3, temperature: 11.9° C.), which was not added with water. It turned out that after 5 hours since beginning of the operation, crystals began to deposit on the heat transfer surface of the crystallizer with the production rate decreasing gradually and after 23 hours the operation was forced to stop.
  • NVP NVP was purified according to the method shown in FIG. 2 .
  • Crystallization was carried out in the same way as Example II-1 except that distilled NVP of a water content of 0.03% by weight and a purity of 99.43% was mixed with the NVP of a water content of 0.69% by weight and a purity of 98.33% recovered from a crystallization mother liquor at a mixing ratio of 4:6 by weight to obtain feed NVP (pH: 10.3, temperature: 6.5° C.).
  • the crystallization mother liquor was taken out of the system at a rate of 4 L/h to prevent quality deterioration of the NVP, but water was not added. It turned out that after 3 hours since beginning of the operation, crystals began to deposit on the heat transfer surface of the crystallizer with the production rate decreasing gradually and after 11 hours the operation was forced to stop.
  • NVP NVP was purified according to the method shown in FIG. 2 .
  • Distilled NVP of a water content of 0.02% was mixed with the mother liquor of a water content of 0.47% recovered from a horizontal multistage cooling crystallizer at a mixing ratio of about 1:6 (by weight) and then added with water to obtain feed NVP adjusted to be of a water content of 1.75% by weight, a pH of 11.7 and a temperature of 13.0° C., which was continuously supplied to the crystallizer.
  • Crystallization was carried out under the conditions of a feed rate of 75 kg/h, a slurry concentration of 20%, a temperature of 7.0° C. and a retention time of 4 hours.
  • NVP of a purity of not lower than 99.98% could be stably obtained without depositing of crystals on the heat transfer surface of the crystallizer.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)
US11/918,228 2005-04-11 2006-04-07 Production Method of N-Vinyl-2-Pyrrolidone Abandoned US20090088579A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2005113523 2005-04-11
JP2005-113523 2005-04-11
JP2005218778 2005-07-28
JP2005-218778 2005-07-28
PCT/JP2006/307892 WO2006109869A1 (en) 2005-04-11 2006-04-07 Production method of n-vinyl-2-pyrrolidone

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2006/307892 A-371-Of-International WO2006109869A1 (en) 2005-04-11 2006-04-07 Production method of n-vinyl-2-pyrrolidone

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/109,450 Continuation US9096516B2 (en) 2005-04-11 2011-05-17 Production method of N-vinyl-2-pyrrolidone

Publications (1)

Publication Number Publication Date
US20090088579A1 true US20090088579A1 (en) 2009-04-02

Family

ID=37087130

Family Applications (2)

Application Number Title Priority Date Filing Date
US11/918,228 Abandoned US20090088579A1 (en) 2005-04-11 2006-04-07 Production Method of N-Vinyl-2-Pyrrolidone
US13/109,450 Active US9096516B2 (en) 2005-04-11 2011-05-17 Production method of N-vinyl-2-pyrrolidone

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/109,450 Active US9096516B2 (en) 2005-04-11 2011-05-17 Production method of N-vinyl-2-pyrrolidone

Country Status (5)

Country Link
US (2) US20090088579A1 (zh)
EP (2) EP2336106B1 (zh)
JP (1) JP4976311B2 (zh)
CN (1) CN101155779B (zh)
WO (1) WO2006109869A1 (zh)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2835365A1 (en) 2013-08-06 2015-02-11 S.P.C.M. Sa A process to produce N-ethenyl-N-alkyl-alkylamides
CN114685402A (zh) * 2020-12-30 2022-07-01 南通醋酸化工股份有限公司 一种共熔结晶法制备高品质双乙烯酮的方法

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10301230B2 (en) * 2014-05-12 2019-05-28 Gary David McKnight Efficiency of man-made and/or natural organic based animal manure fertilizers by liberating the bound nutrients (macro and micro) through the use of organic, non-aqueous liquid delivery formulations containing organic poly (organicacids) and/or their salts
US10464858B2 (en) * 2015-05-13 2019-11-05 World Source Enterprises, Llc Non-aqueous organo liquid delivery systems containing dispersed poly (organic acids) that improve availability of macro and micro-nutrients to plants
ES2933348T3 (es) * 2018-11-27 2023-02-06 Boai Nky Medical Holdings Ltd Uso de un inhibidor de la polimerización para un monómero de N-vinilpirrolidona
CN113144660B (zh) * 2021-02-05 2023-03-03 成都思达能环保设备有限公司 一种结晶方法及系统
CN113444029B (zh) * 2021-07-03 2023-10-24 乌兰察布市珂玛新材料有限公司 一种n-乙烯基吡咯烷酮精制系统及工艺

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5039817A (en) * 1987-10-29 1991-08-13 Basf Aktiengesellschaft Preparation of pure N-vinyl-2-pyrrolidone
US5329021A (en) * 1993-02-04 1994-07-12 Isp Investments Inc. Process for the production of pure vinyl pyrrolidone
US5710284A (en) * 1995-10-02 1998-01-20 Basf Aktiengesellschaft Purification of N-vinylpyrrolidone by crystallization
US6436243B1 (en) * 1999-10-22 2002-08-20 Nippon Shokubai Co Ltd Process for recovering N-vinyl-2-pyrrolidone
US20030166947A1 (en) * 2000-05-26 2003-09-04 Bernd Eck Method for obtaining pure n-vinyl pyrrolidone
US20030176712A1 (en) * 2002-02-20 2003-09-18 Nippon Shokubai Co., Ltd. Method for preparing deodorized N-vinyl-2-pyrrolidone
US20040133015A1 (en) * 2001-05-10 2004-07-08 Ulrich Hammon Method of purifying a raw melt of at least one monomer by crystallization
US7138528B2 (en) * 2005-02-01 2006-11-21 Lyondell Chemical Technology, L.P. Method for crystallizing N-vinyl-2-pyrrolidone
US20060281928A1 (en) * 2003-05-21 2006-12-14 Hideto Sugiura Process for rectifying n-vinyl-2-pyrrolidone

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003238532A (ja) * 2002-02-20 2003-08-27 Nippon Shokubai Co Ltd Ｎ−ビニル−２−ピロリドンの精製方法
JP2004345993A (ja) 2003-05-21 2004-12-09 Nippon Shokubai Co Ltd Ｎ−ビニル−２−ピロリドンの精製方法、および精製されたｎ−ビニル−２−ピロリドン
JP4269777B2 (ja) * 2003-05-21 2009-05-27 Ｊｓｒ株式会社 新規な芳香族スルホン酸エステル誘導体、ポリアリーレン、スルホン酸基を有するポリアリーレンおよびその製造方法、ならびに高分子固体電解質およびプロトン伝導膜

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5039817A (en) * 1987-10-29 1991-08-13 Basf Aktiengesellschaft Preparation of pure N-vinyl-2-pyrrolidone
US5329021A (en) * 1993-02-04 1994-07-12 Isp Investments Inc. Process for the production of pure vinyl pyrrolidone
US5710284A (en) * 1995-10-02 1998-01-20 Basf Aktiengesellschaft Purification of N-vinylpyrrolidone by crystallization
US6436243B1 (en) * 1999-10-22 2002-08-20 Nippon Shokubai Co Ltd Process for recovering N-vinyl-2-pyrrolidone
US20030166947A1 (en) * 2000-05-26 2003-09-04 Bernd Eck Method for obtaining pure n-vinyl pyrrolidone
US6703511B2 (en) * 2000-05-26 2004-03-09 Basf Aktiengesellschaft Method for obtaining pure n-vinyl pyrrolidone
US20040133015A1 (en) * 2001-05-10 2004-07-08 Ulrich Hammon Method of purifying a raw melt of at least one monomer by crystallization
US20030176712A1 (en) * 2002-02-20 2003-09-18 Nippon Shokubai Co., Ltd. Method for preparing deodorized N-vinyl-2-pyrrolidone
US20060281928A1 (en) * 2003-05-21 2006-12-14 Hideto Sugiura Process for rectifying n-vinyl-2-pyrrolidone
US7138528B2 (en) * 2005-02-01 2006-11-21 Lyondell Chemical Technology, L.P. Method for crystallizing N-vinyl-2-pyrrolidone

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Myerson (Handbook of Industrial Crystallization, 2nd ed. (2002), 313 pages). *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2835365A1 (en) 2013-08-06 2015-02-11 S.P.C.M. Sa A process to produce N-ethenyl-N-alkyl-alkylamides
CN114685402A (zh) * 2020-12-30 2022-07-01 南通醋酸化工股份有限公司 一种共熔结晶法制备高品质双乙烯酮的方法

Also Published As

Publication number Publication date
JP2008535772A (ja) 2008-09-04
EP1868992B1 (en) 2011-06-22
JP4976311B2 (ja) 2012-07-18
EP2336106A1 (en) 2011-06-22
EP2336106B1 (en) 2014-07-16
WO2006109869A1 (en) 2006-10-19
CN101155779A (zh) 2008-04-02
CN101155779B (zh) 2011-03-23
EP1868992A4 (en) 2009-11-25
US20110218344A1 (en) 2011-09-08
EP1868992A1 (en) 2007-12-26
US9096516B2 (en) 2015-08-04

Similar Documents

Publication Publication Date Title
US9096516B2 (en) Production method of N-vinyl-2-pyrrolidone
CA2445063C (en) Crystallization method for production of purified aromatic dicarboxylic acids
JP6579957B2 (ja) 天然バニリンの精製方法
JP4960358B2 (ja) ヨウ素化フェニル誘導体の連続晶出方法
US20110124855A1 (en) Method for isolation of laurolactam from a laurolactam synthesis process stream
KR20140045599A (ko) 요오드화 페닐 유도체의 연속 결정화 방법
JP4949383B2 (ja) 高純度ビニレンカーボネートおよびビニレンカーボネートの精製方法
JP3716009B2 (ja) 炭酸ジフエニルの精製方法
US6703511B2 (en) Method for obtaining pure n-vinyl pyrrolidone
US20090163684A1 (en) Method for purifying polar vinyl compounds
US6414190B1 (en) Purification of acrylic acid by crystallization by means of vacuum evaporation
US20090131687A1 (en) Method of storing and transporting vinylene carbonate
JPH0134214B2 (zh)
EP1636180B1 (en) Process for rectifying n-vinyl-2-pyrrolidone
JP3674010B2 (ja) パラフェニレンジイソシアナートの製造方法
KR101828000B1 (ko) (메트)아크릴산의 회수 방법 및 회수 장치
CN115991673A (zh) 一种瑞戈非尼的纯化方法
KR20240122486A (ko) 조 메틸 메타크릴레이트의 정제를 위한 공정
CN115806465A (zh) 一种混合二氯苯的分离方法
CN117986224A (zh) 一种高纯dmdo的精制方法
JP2000229940A (ja) 高純度ピロリドン類の製造法
EP0757047A2 (en) Process for crystallizing chroman-I from an impure mixture
JP2004345993A (ja) Ｎ−ビニル−２−ピロリドンの精製方法、および精製されたｎ−ビニル−２−ピロリドン
JPH07126234A (ja) 難融解性なα−ヒドロキシイソ酪酸アミド結晶の取得方法
NO342021B1 (no) Kontinuerlig krystalliseringsprosess

Legal Events

Date Code Title Description
AS Assignment

Owner name: NIPPON SHOKUBAI CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SUGIURA, HIDETO;INAOKA, TORU;NOZAKI, SHIGEYUKI;AND OTHERS;REEL/FRAME:020005/0214;SIGNING DATES FROM 20070927 TO 20071009

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION