Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
  • C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
  • C07C37/685—Processes comprising at least two steps in series
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
  • C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
  • C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
  • C07C37/74—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by distillation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
  • C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
  • C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
  • C07C37/84—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by crystallisation

Definitions

• This invention relates to an economical process for the production of high grade bisphenol A which is excellent in color hue and which is thermally stable and is not colored at a high temperature.
• One known method of producing bisphenol A includes a step of introducing crude BPA, which contains impurities such as reaction by-products, into a crystallizer to form crystals of an adduct of BPA with phenol and a mother liquor.
• the crystals separated from a mother liquor are introduced into a dephenolation step to remove phenol and to yield high purity BPA.
• Most of the mother liquor is recycled to a reaction zone while a portion thereof is purged and treated to obtain a purified mother liquor and a residual tar.
• the purified mother liquor is recycled to the reaction zone.
• the crude BPA also contains an acid contaminant which causes decomposition of BPA and production of phenol and isopropenyl phenol during distillation, crystallization, and other steps. Thus, it is undesirable to let the acid contaminant to accumulate in the system. In the above process, the acid contaminant may be discharged from the system together with the tar. However, in order to maintain the concentration of the acid contaminant in the process line at an acceptable level, it is necessary to increase the purge flow rate of tar purge to exhaust the acid contaminant with process fluid containing phenol, impurities like 2, 4' -BPA, etc. This operation causes a problem of an increase in BPA production costs .
• the present invention has been made in view of the above problem and is aimed to provide an economical process which can reduce raw material phenol consumption without adversely affecting the grade of product BPA.
• step (e) recycling a first portion of said mother liquor to step (a) as part of said feed;
• step (g) recycling said purified liquor to step (a) as part of said feed;
• step (h) subjecting at least one of (i) at least part of said feed, (ii) at least part of said product stream and (iii) at least part of said first portion of said mother liquor to a treatment for removing the acid contaminant contained therein, so that the concentration of the acid contaminant in said bottom stream to be supplied to step (c) is maintained within a range of 0.001-0.5 meq/L.
• Fig. 1 is a flow sheet for a system suited for carrying out a process of producing BPA in accordance with the present invention.
• a reactor to which a feed containing raw materials (mixture of phenol and acetone) from a line 11 is fed through lines 13 and 15.
• a strong acid catalyst such as a sulfonic acid-type cation exchange resin.
• the reaction is generally carried out at a temperature of 45-95 °C, preferably 55-85°C.
• the reaction pressure has little influence upon the BPA producing reaction and is not specifically limited.
• the reaction pressure is preferably in the range of 0.05-0.5 MPa from the standpoint of required mechanical strength of the reactor or avoidance of catalyst crush.
• the sulfonic acid-type cation exchange resin is preferably in the form of a gel and is partially modified with a sulfur-containing compound, preferably a compound having a mercapto group and a tertiary nitrogen-containing group, such as mercaptoalkylpyridine or mercaptoalkylamine
• a sulfur-containing compound preferably a compound having a mercapto group and a tertiary nitrogen-containing group, such as mercaptoalkylpyridine or mercaptoalkylamine
• the sulfur-containing compounds include 2- mercaptoethylamine and 2, 2-dimethylthiazolidine .
• the modification of the cation exchange resin may be performed by reacting the resin with a sulfur-containing compound in water or in an organic solvent such that a part of, generally 3-30 % of, preferably 5-15 % of, the sulfonic acid groups are modified with the sulfur-containing compound.
• the catalyst is preferably in the form of particles and packed in a cylindrical reactor.
• the average particle diameter of the catalyst particles is preferably 0.2-2.0 mm, more preferably 0.4-1.5 mm with the uniformity of particle diameter distribution being in the range of 1.0- 1.4, preferably 1.0-1.3.
• the average particle diameter herein and the uniformity of particle diameter distribution are as measured in the state where the catalyst particles are swollen with water.
• the uniformity of particle diameter distribution Z is defined by the formula:
• a and B are the sizes of openings of sieves through which 40 volume % and 90 % by volume of the catalyst particles remain unpassed, respectively.
• the reaction mixture in the reactor 1 is discharged therefrom as a product stream through a line 17.
• the product stream which contains bisphenol A, phenol, unreacted acetone, an acid contaminant or free acid derived from the acid catalyst, reaction by-products, etc. is fed through a line 20 to a distillation zone 2, such as a distillation tower and/or an evaporator, where a distillate containing water, unreacted acetone and part of phenol is separated and discharged through a line 21.
• a bottom stream from the distillation zone 2 containing bisphenol A, phenol and an acid contaminant is fed through a line 22 to a crystallizing zone 3, where the bottom stream is cooled to form crystals of adduct of bisphenol A with phenol.
• the crystals are separated from the mother liquor containing an acid contaminant and phenol and then sent to a next dephenolation step 8 through a line 23.
• the crystallization is repeated two or more times .
• the crystallization in the crystallizing zone 3 is performed in a series of first and second crystallization stages and wherein crystals obtained in the first crystallization stage are dissolved in phenol, suitably a mother liquor separated from the second crystallization stage, the resulting solution being subjected to crystallization in the second crystallization stage .
• the first crystallization stage is preferably carried out using a series of two, first and second crystallizers in such a manner that the bottom stream from the distillation zone is cooled to form relatively large crystals (pure seed crystals) of the adduct crystals having less than 30 % by weight of a content of fine crystals with a diameter of 100 ⁇ m or less.
• the seed crystals-containing slurry in the first crystallizer is fed to the second crystallizer and cooled at a temperature lower than the temperature of the first crystallizer to grow the seed crystals and to form adduct crystals having less than 30 % by weight of a content of fine crystals with a diameter of 100 ⁇ m or less.
• the crystals formed in the second crystallizer are separated from the mother liquor and are dissolved with phenol again.
• the solution is crystallized in the second crystallization stage which is also preferably carried out using a series of two, third and fourth crystallizers.
• the solution is fed to the third crystallizer and cooled to form relatively large crystals (pure seed crystals) of the adduct having less than 30 % by weight of a content of fine crystals with a diameter of 100 ⁇ m or less.
• the seed crystals-containing slurry in the third crystallizer is fed to the fourth crystallizer and cooled at a temperature lower than the third crystallizer temperature to grow the seed crystals and to form crystals having less than 30 % by weight of a content of fine crystals with a diameter of 100 ⁇ m or less.
• the crystals formed in the fourth crystallizer are separated from the mother liquor, melted by heat and sent to a next dephenolation step.
• the mother liquor obtained in the second crystallization stage is preferably used to dissolve the adduct crystals obtained in the first crystallization stage.
• the melted crystals of the adduct of bisphenol A with phenol obtained in the crystallizing zone 3 are sent to the dephenolation step 8, where the phenol is removed from said crystals to yield bisphenol A which is recovered through a line 32.
• the dephenolation may be carried out by any suitable known method.
• the dephenolation is performed by melting the crystals to form a melt containing bisphenol A and phenol, the resulting melt being heated to evaporate the phenol.
• the evaporation may be followed by stripping, for example, steam stripping.
• the melt be contacted with a cation donating solid to neutralize a strong acid contained in the melt with the cation donating solid.
• a cation donating solid to neutralize a strong acid contained in the melt with the cation donating solid.
• the mother liquor obtained in the crystallizing zone 3 is generally composed of 8-12 % by weight of bisphenol A, 75-90 % by weight of phenol and 5-15 % by weight of impurities such as acid contaminant, polyphenols such as trisphenol and coumarone compounds .
• Most of the mother liquor is recycled through lines 24, 31, 12, 13 and 16 to the reactor 1 as part of the feed.
• Another, remainder portion of the mother liquor, which is 0.5-5 parts by weight per 100 parts by weight of the mother liquor, is fed to a purge recovering zone 4 through a line 25.
• the liquid is treated to purge tarry compounds and to recover a purified mother liquor. Acid compounds are also separated from the mother liquor.
• the purge recovering zone 4 includes a phenol distillation tower, a reactor provided with an evaporator operated under vacuum conditions and a strong acid-type ion exchange resin-containing tower. In the purge recovering zone 4, the mother liquor stream 25 is first fed to the distillation tower to recover a phenol as distillate.
• the bottom stream, concentrated mother liquor, is introduced into the reactor with added basic catalyst, where bisphenol, trisphenol and other polyphenols contained in the bottom stream are thermally cracked into isopropenylphenol and phenol by the catalyst, while the impurities such as chromans compounds are polycondensed to form high boiling matters, tar.
• the recovered vapors of isoprophenyl phenol and phenol from the reactor are introduced into the condenser where the vapors are contacted with the distillate from the distillation tower and condensed.
• the condensed stream is then fed to the strong acid-type ion exchange resin-containing tower so that bisphenol A is formed as a result of the reaction of phenol with isopropynyl phenol.
• the effluent from the tower represents the purified liquor obtained from the purge recovering zone 4 and is recycled to the reactor 1 through lines 27, 12, 13 and 16.
• the high boiling matters obtained in the reactor is discharged as residual tar through a line 26.
• the tar from the line 26 may be used as a fuel oil by being mixed and diluted with an ether byproducts oil including aromatic ether obtained from a phenol production process.
• the tar at 180-230°C is fed to a mixing zone to which the dilutant by-products oil including aromatic ether at 60-170 °C is fed for mixing with the tar.
• the mixing ratio of the dilutant to the tar is 0.1:1 to 2:1.
• the mixture discharged from the mixing zone is cooled so that the temperature of the cooled mixture is 80-150°C. A portion of the cooled mixture is recycled to the mixing zone, with the remainder portion being recovered as the fuel oil .
• the concentration of the acid contaminant in the stream 22 to be supplied to the crystallizing zone 3 should be maintained within a range of 0.001-0.5 meq/L
• the lower limit of the acid contaminant concentration is 0.001 meq/L from the economical viewpoint, since a giant acid removing system is required in order to reduce the concentration of the acid contaminant in the bottom stream to an extremely low level.
• the acid contaminant may be removed by contacting the acid contaminant-containing fluid with an absorbent which scarcely elutes impurities.
• absorbents include activated carbon, alkaline inorganic oxides and anion exchange resins.
• the anion exchange resins are preferably used. While various kinds of anion exchange resins can be suitably used for the purpose of the present invention, the use of anion exchange resins having weak basic anion exchanging groups such as primary, secondary or tertiary amines is preferred.
• suitable anion exchange resins are Amberlite ' (manufactured by Rohm and Haas Company) , Dowex (manufactured by Dow Chemical Inc.) and Diaion (manufactured by Mitsubishi Chemical Company) .
• a portion or all of the feed in the line 13 is introduced through a line 14 into an acid treatment zone 5 and fed to the reactor 1 through a line 15
• a portion or all of the product stream in the line 17 is introduced through a line 18 into an acid treatment zone 6 and fed to the distilling zone 2 through a line 19
• a portion or all of the mother liquor in the line 28 is introduced through a line 29 into an acid treatment zone 7 and fed to the reactor 1 through a line 31.
• one or two of the above treatment zones 5, 6 and 7 can be omitted, if desired. It is preferred that the acid contaminant be removed only in the acid treatment zone 7 from the economical standpoint. Because the concentration of the acid contaminant per unit volume of the stream in the line 28 is higher than that in the line 13, 14, 17 and 18, the acid removal in the zone 7 is more effective and efficient than in the zone 5 or 6.
• the amount of the stream to be treated in each of the acid removing zones 5-7 may be suitably determined according to the concentration of the acid contaminant in the stream to be treated.
• the flow rate of the stream 25 to purge recovery zone 4 should be increased to remove acid contaminant, since the acid contaminants in the process stream are removed in at least one of the acid removing zones 5-7.
• the treatment in the purge recovery zone 4 may be carried out only for the purpose of reducing impurities other than acid contaminants.
• the quality of the crystals of the adduct obtained in the crystallization zone 3 is not adversely affected.
• the amount of the tars discharged through the line 26 can be reduced.
• the acid treatment in the present invention is performed such that the concentration of the acid contaminant in the bottom stream to be supplied to the crystallizing zone is maintained within a range of 0.001-0.5 meq/L, the operation load in the acid removal step can be reduced and the amount of the absorbent in the acid treatment can be reduced. Thus, the acid can be removed with reduced costs .
• Phenol 89.5 % Free acid: below measurable limit
• Absorbent Anion exchange resin having secondary amines (Amberlite manufactured by Rohm & Haas).
• Phenol below 15 ppm by weight
• Example 1 was repeated in the same manner as described except that the acid removal treatment at zone 7 was not carried out.
• the mother liquor in the line 28 was directly passed to the line 31 and fed to the reactor 1.
• the concentration of the free acid (acid contaminant) in the bottom stream in the line 22 was higher than 0.101 meq/L.
• the amount of tars discharged through the line 26 increased to 0.7 kg/h.
• the BPA production cost was thus higher than that in Example 1.
• Example 1 was repeated in the same manner as described except that the acid removal treatment at zone 7 was not carried out and that the amount of the mother liquor purged through the line 25 was reduced to 0.5 kg/h. In this case the amount of tars discharged through the line 26 was 0.05 kg/h. However, the concentration of the free acid in the bottom stream in the line 22 increased above 2.0 meq/L, so that BPA decomposed in dephenolation stage 8. The BPA product recovered through the line 32 had a phenol concentration of 100-1000 ppm by weight.

Priority Applications (1)

Applications Claiming Priority (2)

Publications (1)

Family

ID=18642275

Family Applications (1)

Country Status (5)

Families Citing this family (10)

Citations (13)

• 2000
  • 2000-05-02 JP JP2000133873A patent/JP4140171B2/ja not_active Expired - Lifetime
• 2001
  • 2001-04-26 AU AU2001252614A patent/AU2001252614A1/en not_active Abandoned
  • 2001-04-26 CN CNA01812223XA patent/CN1738787A/zh active Pending
  • 2001-04-26 WO PCT/JP2001/003660 patent/WO2001083416A1/en active Application Filing
  • 2001-04-26 KR KR1020027014618A patent/KR100786042B1/ko active IP Right Grant

Patent Citations (13)

Also Published As

Similar Documents

Legal Events