Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/04—Aromatic polycarbonates
  • C08G64/06—Aromatic polycarbonates not containing aliphatic unsaturation
• • 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
  • C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
  • C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
• • 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
  • C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
  • C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
  • C07C39/14—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with at least one hydroxy group on a condensed ring system containing two rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
  • C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
  • C07C39/15—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with all hydroxy groups on non-condensed rings, e.g. phenylphenol
  • C07C39/16—Bis-(hydroxyphenyl) alkanes; Tris-(hydroxyphenyl)alkanes
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
  • C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
  • C07C39/17—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings containing other rings in addition to the six-membered aromatic rings, e.g. cyclohexylphenol
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/04—Aromatic polycarbonates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/20—General preparatory processes
  • C08G64/30—General preparatory processes using carbonates
  • C08G64/307—General preparatory processes using carbonates and phenols
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/42—Chemical after-treatment
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
  • C07C2601/14—The ring being saturated
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2602/00—Systems containing two condensed rings
  • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
  • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
  • C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane

Definitions

• the present invention relates to a bisphenol composition, a polycarbonate resin, and a method for producing the same.
• the bisphenol composition of the present invention is useful as a resin raw material such as a polycarbonate resin, an epoxy resin, and an aromatic polyester resin, and as an additive for a curing agent, a color developer, a fading inhibitor, and other bactericidal agents and antibacterial and antifungal agents. Is.
• Bisphenol is useful as a raw material for polymer materials such as polycarbonate resin, epoxy resin, and aromatic polyester resin.
• polymer materials such as polycarbonate resin, epoxy resin, and aromatic polyester resin.
• typical bisphenols for example, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxy-3-methylphenyl) propane and the like are known (Patent Documents 1 and 2). ).
• Polycarbonate resin which is a typical use of bisphenol, is required to be colorless and transparent.
• the color tone of the polycarbonate resin is greatly affected by the color tone of the raw material. Therefore, the color tone of bisphenol, which is a raw material, is also required to be colorless. Since it is difficult to directly quantify the color of bisphenol, in the present invention, bisphenol is dissolved in methanol to quantify the color difference, and this color tone is referred to as "methanol-dissolved color".
• thermal color tone stability In the production of the polycarbonate resin, since the polymerization reaction is carried out after the bisphenol is melted, thermal color stability before the start of the polymerization is also required. In the present invention, this color tone is referred to as "thermal color tone stability”.
• the polycarbonate resin there is a demand for a polycarbonate resin having the molecular weight as designed and having a good color tone.
• bisphenol as a raw material is required to have excellent methanol-dissolved color, melt color difference, and thermal color stability, and also have excellent thermal decomposition stability.
• the present inventor has found that a bisphenol C composition containing a specific compound in a predetermined ratio is excellent in methanol dissolution color, melt color difference, thermal color tone stability, and thermal decomposition stability. Further, the present inventor has found that a polycarbonate resin containing a structural unit derived from this specific compound in a predetermined ratio is excellent in color tone. That is, the gist of the present invention lies in the following [1] to [14].
• X is a single bond, -CR 11 R 12 -, - O -, - CO -, - S -, - SO-, or -SO 2 - shows a.
• R 11 and R 12 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R 11 and R 12 may be combined to form a ring.
• X is a single bond, -CR 11 R 12 -, - O -, - CO -, - S -, - SO-, or -SO 2 - shows a.
• R 11 and R 12 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R 11 and R 12 may be combined to form a ring.
• the bisphenol represented by the general formula (II) is 2- (4-hydroxy-3-methylphenyl) -2- (4-hydroxy-3,5-dimethylphenyl) propane, 1- (4- (4-). Hydroxy-3-methylphenyl) -1- (4-hydroxy-3,5-dimethylphenyl) cyclohexane, and 1- (4-hydroxy-3-methylphenyl) -1- (4-hydroxy-3,5-)
• the bisphenol composition according to any one or more of [1] to [3] selected from the group consisting of dimethylphenyl) -3,3,5-trimethylcyclohexane.
• the bisphenol represented by the general formula (I) is 2,2-bis (4-hydroxy-3-methylphenyl) propane, 1,1-bis (4-hydroxy-3-methylphenyl) cyclohexane, and the like. And any one or more of [1] to [8] selected from the group consisting of 1,1-bis (4-hydroxy-3-methylphenyl) -3,3,5-trimethylcyclohexane.
• a polycarbonate resin having at least a repeating structural unit represented by the following general formula (A) and obtained by alkaline hydrolysis of the polycarbonate resin is represented by the following general formula (I).
• R 1 to R 6 are independently hydrogen atoms, halogen atoms, alkyl groups, alkoxy groups, or aryl groups, and the alkyl groups, alkoxy groups, and aryl groups are substituted or absent. It may be any of the substitutions.
• R 5 and R 6 may be bonded or crosslinked with each other between the two groups, or R 5 and R 6 may be bonded together with adjacent carbon atoms to contain a heteroatom.
• An alkylidene group may be formed.
• X is a single bond, -CR 11 R 12 -, - O -, - CO -, - S -, - SO-, or -SO 2 - shows a.
• R 11 and R 12 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R 11 and R 12 may be combined to form a ring.
• X is a single bond, -CR 11 R 12 -, - O -, - CO -, - S -, - SO-, or -SO 2 - shows a.
• R 11 and R 12 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R 11 and R 12 may be combined to form a ring.
• a bisphenol composition having good methanol dissolution color, melt color difference, thermal color tone stability, and thermal decomposition stability is provided.
• a polycarbonate resin obtained by using this bisphenol composition that is, a polycarbonate resin obtained by obtaining the specific compound in a predetermined ratio by alkaline hydrolysis, provides a polycarbonate resin having an excellent color tone.
• the bisphenol composition of the present invention is a bisphenol composition containing 95% by mass or more of bisphenol, and the bisphenol represented by the following general formula (II) in the bisphenol composition (hereinafter referred to as "bisphenol (II)").
• the content of (may be referred to as) is 150 mass ppm or more, and the methanol-dissolved color (Hazen color number) of the bisphenol composition is 2 or less.
• X is a single bond, -CR 11 R 12 -, - O -, - CO -, - S -, - SO-, or -SO 2 - shows a.
• R 11 and R 12 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R 11 and R 12 may be combined to form a ring.
• the content of bisphenol (II) in the bisphenol composition of the present invention is preferably 200 mass ppm or more, more preferably 250 mass ppm or more, particularly preferably 300 mass ppm or more, preferably 20000 mass ppm or less, more preferably. Is 15,000 mass ppm or less, more preferably 1400 mass ppm or less, and particularly preferably 1300 mass ppm or less.
• the content of bisphenol (II) in the bisphenol composition is less than the above lower limit, it is not possible to obtain a bisphenol composition having good methanol dissolution color, melt color difference, thermal color tone stability, and thermal decomposition stability.
• the content of bisphenol (II) in the bisphenol composition exceeds the above upper limit, there is a tendency as follows. 1) When producing a polycarbonate resin, the molar ratio with diphenyl carbonate shifts, which affects the polymerization reaction. 2) The brittleness (izod) of the polycarbonate resin obtained by using this bisphenol composition is reduced, and the high surface hardness peculiar to the polycarbonate resin containing the structural unit derived from bisphenol (I) described later is reduced.
• bisphenol (II) examples include 2- (4-hydroxy-3-methylphenyl) -2- (4-hydroxy-3,5-dimethylphenyl) propane and 1- (4-hydroxy-3-methyl). Phenyl) -1- (4-hydroxy-3,5-dimethylphenyl) cyclohexane, and 1- (4-hydroxy-3-methylphenyl) -1- (4-hydroxy-3,5-dimethylphenyl) -3 , 3,5-Trimethylcyclohexane, any one or more selected from the group. Of these, 2- (4-hydroxy-3-methylphenyl) -2- (4-hydroxy-3,5-dimethylphenyl) propane (hereinafter referred to as "trimethylbisphenol A”) is particularly preferable.
• the detection and quantification of bisphenol (II) can be performed using a standard reverse phase column for high-speed analysis with a particle size of 3 ⁇ m.
• the content of bisphenol (II) in the bisphenol composition can be adjusted by adding an appropriate amount of bisphenol (II) to bisphenol that does not contain or contains a low concentration of purified bisphenol (II). Further, as will be described later, a bisphenol product containing bisphenol (II) can be prepared as the bisphenol composition of the present invention by producing bisphenol (II) together with bisphenol in the reaction system during the production of bisphenol.
• the bisphenol contained in the bisphenol composition of the present invention is usually a compound represented by the following general formula (1).
• R 1 to R 6 in the general formula ( 1 ) are synonymous with R 1 to R in the general formulas (3) and (4) described later, and suitable examples and specific examples thereof are the general formula (3) described later. , (4).
• bisphenol represented by the above general formula (1) examples include 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxy-3-methylphenyl) propane, and 2, 2-Bis (4-hydroxy-3,5-dimethylphenyl) propane, 1,1-bis (4-hydroxy-3-methylphenyl) cyclohexane, 1,1-bis (4-hydroxy-3-methylphenyl)- 3,3,5-trimethylcyclohexane, 9,9-bis (4-hydroxy-3-methylphenyl) fluorene, 3,3-bis (4-hydroxyphenyl) pentane, 3,3-bis (4-hydroxy-3) -Methylphenyl) pentane, 2,2-bis (4-hydroxyphenyl) pentane, 2,2-bis (4-hydroxy-3-methylphenyl) pentane, 3,3-bis (4-hydroxyphenyl) heptane, 3 , 3-bis (4-hydroxy-3-methylphenyl) heptane, 2,2-bis (4-hydroxyphenyl) heptane
• bisphenol contained in the bisphenol composition of the present invention bisphenol represented by the following general formula (I) (hereinafter, may be referred to as "bisphenol (I)”) is preferable.
• bisphenol (I) include 2,2-bis (4-hydroxy-3-methylphenyl) propane, 1,1-bis (4-hydroxy-3-methylphenyl) cyclohexane, and 1,1-bis (4). Any one or more selected from the group consisting of -hydroxy-3-methylphenyl) -3,3,5-trimethylcyclohexane is preferable.
• 2,2-bis (4-hydroxy-3-methylphenyl) propane (bisphenol C) is preferable.
• X is a single bond, -CR 11 R 12 -, - O -, - CO -, - S -, - SO-, or -SO 2 - shows a.
• R 11 and R 12 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R 11 and R 12 may be combined to form a ring.
• the bisphenol composition of the present invention contains such bisphenol in an amount of 95% by mass or more, preferably 99% by mass or more, and more preferably 99.5% by mass or more. If the content of bisphenol is less than the above lower limit, it is not preferable for use as bisphenol.
• the upper limit of the content of bisphenol in the bisphenol composition of the present invention is to secure the content of bisphenol (II), from the viewpoint of production cost, etc., to adjust the ratio of the physical property to diphenyl carbonate in the production reaction of the polycarbonate resin, and the surface hardness. From the viewpoint of mechanical properties of the polycarbonate resin such as brittleness and brittleness, it is usually about 99.9% by mass.
• the detection and quantification of bisphenol can be performed using a standard reverse phase column for high-speed analysis.
• ⁇ Methanol-dissolved color of bisphenol composition The methanol-dissolved color of the bisphenol composition is used to evaluate the color tone of the bisphenol composition at room temperature. The lower the number of Hazen colors of the methanol-dissolved color of the bisphenol composition, the better the color tone of the bisphenol composition (closer to white). As a cause of deteriorating the dissolved color of methanol in the bisphenol composition, there is an inclusion of an organic coloring component or a metal.
• the methanol-dissolved color of the bisphenol composition is measured at room temperature (about 20 ° C.) after the bisphenol composition is dissolved in methanol to make a homogeneous solution.
• the measuring method include a method of visually comparing with a standard solution having a Hazen color number, or a method of measuring the Hazen color number using a color difference meter such as "SE6000" manufactured by Nippon Denshoku Kogyo Co., Ltd.
• the solvent methanol and bisphenol used here and the mass ratio of the solvent are preferably selected as appropriate depending on the type of bisphenol.
• the number of Hazen colors of the methanol-dissolved color of the bisphenol composition of the present invention is 2 or less, preferably 1 or less, and more preferably 0 or less.
• melt color difference of the bisphenol composition is used to evaluate the color tone of the bisphenol composition at a temperature close to the polymerization temperature of polycarbonate.
• the measurement temperature of the melt color difference is the melting point of bisphenol + 50 ° C.
• the melt color difference of the bisphenol composition indicates that the lower the number of Hazen colors, the better the color tone of the bisphenol composition (closer to white).
• the melt color difference of the bisphenol composition is measured in advance by melting the bisphenol composition at a temperature close to the polymerization temperature and measuring the time when the temperature is stable.
• Examples of the measuring method include a method of visually comparing with a standard solution having a Hazen color number, or a method of measuring the Hazen color number using a color difference meter such as "SE6000" manufactured by Nippon Denshoku Kogyo Co., Ltd.
• the bisphenol composition of the present invention is melted at 190 ° C. for 30 minutes, and the number of Hazen colors measured using "SE6000" manufactured by Nippon Denshoku Kogyo Co., Ltd. is preferably 100 or less, more preferably 30 or less, and particularly. It is preferably 25 or less, and particularly preferably 20 or less.
• the thermal color stability of the bisphenol composition is used to evaluate the thermal stability of the color tone of the bisphenol composition by holding it at a temperature close to the polymerization temperature of polycarbonate for a predetermined time, similar to the melt color difference of the bisphenol composition.
• the measurement temperature of the thermal color stability of the bisphenol composition is the melting point of bisphenol + 50 ° C.
• the thermal color stability of the bisphenol composition As for the thermal color stability of the bisphenol composition, the lower the number of Hazen colors, the better the thermal color stability of the bisphenol composition.
• the causes of deteriorating the thermal color stability of the bisphenol composition include components that are colored by heating and acidic substances and basic substances having a concentration of about several ppm.
• the thermal color stability of the bisphenol composition is measured in advance by melting the bisphenol composition at a temperature close to the polymerization temperature and measuring the time at which the temperature is stable.
• the retention time for thermal color stability of the bisphenol composition is 4 hours. Examples of the measuring method include a method of visually comparing with a standard solution having a Hazen color number, or a method of measuring the Hazen color number using a color difference meter such as "SE6000" manufactured by Nippon Denshoku Kogyo Co., Ltd.
• the number of Hazen colors is preferably 50 or less, more preferably 45 or less, and particularly preferably 35 or less.
• the thermal decomposition stability of the bisphenol composition is used to evaluate the thermal stability of the bisphenol composition by holding it at a temperature close to the polymerization temperature of polycarbonate for a predetermined time, similar to the thermal color stability of the bisphenol composition.
• the preferred measurement temperature for the thermal decomposition stability of the bisphenol composition is the melting point of bisphenol + 50 ° C.
• the thermal decomposition stability of the bisphenol composition indicates that the smaller the amount of the decomposed product produced, the more stable the bisphenol composition is.
• the decomposition product in the thermal decomposition stability of the bisphenol composition depends on the type of bisphenol, but the aromatic alcohol which is the raw material of the bisphenol composition or the addition of the aromatic alcohol and the ketone or aldehyde which is the raw material is used. Can be mentioned.
• causes of deteriorating the thermal decomposition stability of the bisphenol composition include, in addition to the mixing of organic coloring components and metals, components that are colored by heating and acidic substances and basic substances having a concentration of about several ppm.
• Detection and quantification of decomposition products of bisphenol compositions can be performed using a standard reverse phase column for high-speed analysis.
• the amount of isopropenyl cresol produced as a decomposition product of the bisphenol composition as measured in Examples described later is preferably 200 mass ppm or less.
• the methanol-dissolved color of the bisphenol composition is a method for evaluating the color tone of the bisphenol composition itself.
• the bisphenol composition having a good methanol-dissolved color is important. Since the polycarbonate resin inherits the color tone of the raw material, a bisphenol composition having a good color tone is important for the polycarbonate resin that is required to be colorless and transparent.
• the melt polymerization method which is one of the methods for producing a polycarbonate resin
• the bisphenol composition is held in a molten state at a high temperature until the start of the polymerization reaction.
• the substance amount ratio with diphenyl carbonate deviates from the predetermined substance amount ratio, and it is difficult to obtain a polycarbonate resin having polymerization reaction activity and a predetermined molecular weight. Become. Therefore, resistance to thermal decomposition (thermal decomposition stability of the bisphenol composition) is important.
• the methanol-dissolved color of the bisphenol composition is important.
• the melt color difference of the bisphenol composition is important.
• the thermal color stability of the bisphenol composition is important.
• the sodium content in the bisphenol composition of the present invention is preferably less than 0.5 mass ppm, more preferably less than 0.4 mass ppm, and particularly preferably less than 0.3 mass ppm. Since sodium in the bisphenol composition exhibits a catalytic action, a large content thereof deteriorates thermal color stability and thermal decomposition stability. Therefore, the sodium content in the bisphenol composition of the present invention is preferably not more than the above upper limit.
• the sodium content in the bisphenol composition is measured by the method described in the section of Examples below.
• the iron content in the bisphenol composition of the present invention is preferably 0.5 mass ppm or less, more preferably 0.4 mass ppm or less, and particularly preferably 0.3 mass ppm or less.
• Iron in the bisphenol composition has a structure in which bisphenol is coordinated, and therefore has absorption in the visible region. Therefore, the iron becomes a coloring factor of the bisphenol composition, and if the content thereof is large, the methanol-dissolved color and the molten color difference are deteriorated. Further, since the iron exhibits a catalytic action, if its content is large, the thermal color tone stability and the thermal decomposition stability are deteriorated. Therefore, the iron content in the bisphenol composition of the present invention is preferably not more than the above upper limit.
• Examples of the origin of iron in the bisphenol composition of the present invention include iron dissolved in aromatic alcohol, which is a raw material of bisphenol, and iron mixed from the reaction tank and the equipment above the reaction tank during the reaction to produce bisphenol. Be done. Depending on the form of iron, these irons are appropriately removed by a purification method described later, such as repeated washing with water under acidic conditions or repeated washing with basic conditions.
• the iron content in the bisphenol composition is measured by the method described in the section of Examples below.
• the aluminum content in the bisphenol composition of the present invention is preferably 0.1 mass ppm or less, more preferably 0.09 mass ppm or less, and particularly preferably 0.08 mass ppm or less.
• Aluminum in the bisphenol composition has a structure in which bisphenol is coordinated, and therefore has absorption in the visible region. Therefore, the aluminum becomes a coloring factor of the bisphenol composition, and if the content thereof is large, the methanol-dissolved color and the molten color difference are deteriorated. Further, since the aluminum exhibits a catalytic action, if the content thereof is large, the thermal color tone stability and the thermal decomposition stability are deteriorated. Therefore, the aluminum content in the bisphenol composition of the present invention is preferably not more than the above upper limit.
• the origin of aluminum in the bisphenol composition of the present invention is that aluminum dissolved in aromatic alcohol, which is a raw material of bisphenol, was mixed from the outside when the solid bisphenol was obtained and then taken out or supplied to a dryer.
• Examples include aluminum derived from aluminum oxide.
• these aluminums are appropriately removed by a purification method described later, such as repeated washing with water under acidic conditions or repeated washing with basic conditions.
• the aluminum content in the bisphenol composition is measured by the method described in the section of Examples below.
• the method for producing the bisphenol composition of the present invention containing bisphenol, preferably bisphenol (I) in an amount of 95% by mass or more and containing bisphenol (II) in a predetermined ratio is not particularly limited, and examples thereof include the following methods. Be done. (1) Method of adding a predetermined amount of bisphenol (II) to solid bisphenol (I) (2) Method of adding a predetermined amount of bisphenol (II) to molten bisphenol (I) (3) Method of adding bisphenol (I) A method for obtaining a bisphenol (I) product containing bisphenol (II) by producing bisphenol (II) as a by-product during production or by producing bisphenol (II) together with bisphenol (I).
• bisphenol (II) In the method of adding bisphenol (II) to the solid or melted bisphenol (I) of (1) and (2), it is necessary to prepare bisphenol (II) separately. Therefore, (3) bisphenol (II) is by-produced or bisphenol (II) is produced in the reaction system for producing bisphenol (I), and the bisphenol (I) product contains bisphenol (II) in a predetermined ratio. The method is preferred.
• the obtained bisphenol (I) product is further purified by crystallization, suspension washing, sprinkling washing, etc. By removing a part of the bisphenol (II) contained in the bisphenol (I) product, it is possible to control so that the bisphenol (I) product containing the bisphenol (II) within the specified range of the present invention can be obtained. it can.
• a method for producing trimethylbisphenol A together with bisphenol C in the reaction system during the production of bisphenol C to obtain a bisphenol C product containing trimethylbisphenol A as the bisphenol composition of the present invention a ketone or aldehyde and an aromatic alcohol are used as acids.
• acids include a method of producing trimethylbisphenol A together with bisphenol C or bisphenol C by condensing in the presence of a catalyst and a thiol co-catalyst. According to this method, trimethylbisphenol A can be produced in the reaction system. This method will be described below.
• bisphenol C is produced by condensing an aromatic alcohol with a ketone or aldehyde in the presence of an acid catalyst.
• the reaction for producing bisphenol is carried out according to the reaction general formula (2) shown below.
• the raw material aromatic alcohol and the raw material ketone or aldehyde are selected and used so that at least bisphenol C is produced in such a bisphenol production reaction.
• R 1 to R 6 are synonymous with those in the general formula (1).
• the raw material aromatic alcohol used for producing bisphenol is usually a compound represented by the following general formula (3).
• examples of R 1 to R 4 include a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and an aryl group, respectively.
• the alkyl group, alkoxy group, aryl group and the like may be substituted or unsubstituted.
• examples of R 1 to R 4 include hydrogen atom, fluoro group, chloro group, bromo group, iodo group, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group and i-butyl group.
• R 2 and R 3 are preferably hydrogen atoms because the condensation reaction does not easily proceed if they are sterically bulky. It is more preferable that R 1 to R 4 are independently hydrogen atoms or alkyl groups, respectively. It is more preferable that R 1 and R 4 are independently hydrogen atoms or alkyl groups, and R 2 and R 3 are hydrogen atoms.
• Specific examples of the compound represented by the general formula (3) include phenol, cresol, xylenol, ethylphenol, propylphenol, butylphenol, methoxyphenol, ethoxyphenol, propoxyphenol, butoxyphenol, benzylphenol, and phenylphenol. Can be mentioned.
• bisphenol C is produced using orthocresol, or bisphenol C and trimethylbisphenol A are produced using xylenol together with orthocresol.
• ketone or aldehyde The raw material ketone or aldehyde used for producing bisphenol is usually a compound represented by the following general formula (4).
• examples of R 5 and R 6 include a hydrogen atom, an alkyl group, an alkoxy group, and an aryl group, respectively.
• the alkyl group, alkoxy group, aryl group and the like may be substituted or unsubstituted.
• examples of R 5 and R 6 include hydrogen atom, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, i-butyl group, t-butyl group, n-pentyl group, and i.
• -Pentyl group n-hexyl group, n-heptyl group, n-octyl group, 2-ethylhexyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, methoxy group, ethoxy Group, n-propoxy group, i-propoxy group, n-butoxy group, i-butoxy group, t-butoxy group, n-pentyloxy group, i-pentyloxy group, n-hexyloxy group, n-heptyloxy group , N-octyloxy group, n-nonyloxy group, n-decyloxy group, n-undecyloxy group, n-dodecyloxy group, cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohex
• R 5 and R 6 may be bonded or crosslinked with each other between the two groups.
• R 5 and R 6 may be bonded together with adjacent carbon atoms to form a cycloalkylidene group that may contain heteroatoms.
• the cycloalkylidene group is a divalent group obtained by removing two hydrogen atoms from one carbon atom of cycloalkane.
• Examples of the cycloalkylidene group formed by bonding R 5 and R 6 together with adjacent carbon atoms include cyclopropylidene, cyclobutylidene, cyclopentylidene, cyclohexylidene, 3,3,5-trimethyl. Cyclohexylidene, cycloheptylidene, cyclooctylidene, cyclononylidene, cyclodecylidene, cycloundecylidene, cyclododecylidene, fluorenylidene, xantonilidene, thioxanthonidene and the like can be mentioned.
• Specific examples of the compound represented by the general formula (4) include formaldehyde, acetaldehyde, propionaldehyde, butylaldehyde, pentylaldehyde, hexylaldehyde, heptylaldehyde, octylaldehyde, nonylaldehyde, decylaldehyde, undecylaldehyde, and dodecyl.
• Ketones such as aldehydes; ketones such as acetone, butanone, pentanon, hexanone, heptanone, octanon, nonanone, decanone, undecanone, dodecanone; benzaldehyde, phenylmethylketone, phenylethylketone, phenylpropylketone, cresylmethylketone, cleres Arylalkyl Ketones such as Zyrethyl Ketone, Cresylpropyl Ketone, Xylyl Methyl Ketone, Xylyl Ethyl Ketone, Xylylpropyl Ketone, Cyclopropanone, Cyclobutanone, Cyclopentanone, Cyclohexanone, Cycloheptanone, Cyclooctanone, Cyclononanone , Cyclic alcan ketones such as cyclodecanone, cycloundecanone, cyclodo
• At least acetone is used among these.
• the molar ratio of the aromatic alcohol to the ketone or aldehyde is preferably 1.5 or more, more preferably 1.6 or more, still more preferably 1.7 or more, and preferably 15 or less, more preferably. Is 10 or less, more preferably 8 or less.
• ketones and aldehydes As the method for supplying ketones and aldehydes, a method of supplying them all at once and a method of supplying them separately can be used. Since the reaction for producing bisphenol is an exothermic reaction, it is preferable to supply ketones and aldehydes in divided amounts, such as by dropping them little by little.
• acid catalyst examples include aromatic sulfonic acids such as sulfuric acid, hydrochloric acid, hydrogen chloride gas, phosphoric acid and p-toluenesulfonic acid, and aliphatic sulfonic acids such as methanesulfonic acid.
• aromatic sulfonic acids such as sulfuric acid, hydrochloric acid, hydrogen chloride gas, phosphoric acid and p-toluenesulfonic acid
• aliphatic sulfonic acids such as methanesulfonic acid.
• the molar ratio of the acid catalyst to the ketone or aldehyde used for condensation ((number of moles of acid catalyst / number of moles of ketone) or (number of moles of acid catalyst / number of moles of aldehyde)) is small, as the condensation reaction progresses.
• the acid catalyst is diluted by the by-produced water and the reaction takes time. If this molar ratio is high, the amount of ketones or aldehydes may increase. From these facts, the molar ratio of the acid catalyst to the ketone or aldehyde used for condensation is preferably 0.01 or more, more preferably 0.05 or more, still more preferably 0.1 or more, preferably 10 or less, more preferably. Is 8 or less, more preferably 5 or less.
• the acid catalyst shall be any one selected from the group consisting of aromatic sulfonic acids such as sulfuric acid, hydrochloric acid, hydrogen chloride gas, phosphoric acid and p-toluenesulfonic acid, and aliphatic sulfonic acids such as methanesulfonic acid. Is preferable.
• the molar ratio of hydrogen chloride to the ketone or aldehyde used in the reaction ((number of moles of hydrogen chloride / number of moles of ketone) or (number of moles of hydrogen chloride / number of moles of aldehyde)) is small, water produced as a by-product during the condensation reaction Hydrogen chloride is diluted by this and a long reaction time is required. If this molar ratio is large, the amount of ketones or aldehydes may increase. From these facts, the molar ratio of hydrogen chloride to ketone or aldehyde is preferably 0.01 or more, more preferably 0.05 or more, still more preferably 0.1 or more, preferably 10 or less, more preferably 8 or less. , More preferably 5 or less.
• Sulfuric acid is an acidic liquid represented by the chemical formula H 2 SO 4 .
• sulfuric acid is used as an aqueous solution of sulfuric acid diluted with water, and is called concentrated sulfuric acid or dilute sulfuric acid depending on its concentration.
• dilute sulfuric acid is an aqueous sulfuric acid solution having a mass concentration of less than 90% by mass.
• the concentration of sulfuric acid used is preferably 70% by mass or more, more preferably 75% by mass or more, and further preferably 80% by mass or more.
• the upper limit of the concentration of sulfuric acid used is usually 99.5% by mass or less or 99% by mass or less.
• thiol In the production of bisphenol, thiol can be used as a cocatalyst in the reaction of condensing a ketone or aldehyde with an aromatic alcohol.
• thiol as a cocatalyst, for example, in the production of 2,2-bis (4-hydroxy-3-methylphenyl) propane, the production of 24 bodies is suppressed, the selectivity of 44 bodies is increased, and the polycarbonate resin is produced. It is possible to obtain the effect of increasing the polymerization activity at the time and improving the color tone of the obtained polycarbonate resin. Although the details of the reason why the effect of improving the polymerization activity during the production of the polycarbonate resin and the effect of improving the color tone of the obtained polycarbonate resin are exhibited are not clear, the use of thiol produces an inhibitor for the polymerization reaction for producing the polycarbonate resin. It is presumed that this is due to the fact that it is possible to suppress the formation of deteriorating substances as well as
• thiol used as a co-catalyst examples include mercaptocarboxylic acids such as mercaptoacetic acid, thioglycolic acid, 2-mercaptopropionic acid, 3-mercaptopropionic acid and 4-mercaptobutyric acid, methyl mercaptan, ethyl mercaptan, propyl mercaptan and butyl.
• mercaptocarboxylic acids such as mercaptoacetic acid, thioglycolic acid, 2-mercaptopropionic acid, 3-mercaptopropionic acid and 4-mercaptobutyric acid, methyl mercaptan, ethyl mercaptan, propyl mercaptan and butyl.
• Mercaptan Pentyl mercaptan, Hexyl mercaptan, Heptyl mercaptan, Octyl mercaptan, Nonyl mercaptan, Decyl mercaptan (decane thiol), Undecyl mercaptan (undecanthiolu), Dodecyl mercaptan (dodecane thiol), Tridecyl mercaptan, Tetradecyl mercaptan Examples thereof include alkyl thiols such as decyl mercaptan and aryl thiols such as mercaptophenol.
• the thiol cocatalyst is used.
• the effect of improving the reaction selectivity of bisphenol by using it cannot be obtained. If this molar ratio is high, it may be mixed with bisphenol and the quality may deteriorate.
• the molar ratio of the thiol cocatalyst to the ketone and the aldehyde is preferably 0.001 or more, more preferably 0.005 or more, still more preferably 0.01 or more, preferably 1 or less, more preferably 0. It is 5.5 or less, more preferably 0.1 or less.
• the thiol cocatalyst is preferably premixed with a ketone or aldehyde before being subjected to the reaction.
• the method for mixing the thiol with the ketone or aldehyde may be a mixture of the thiol with the ketone or the aldehyde, or a ketone or the aldehyde with the thiol.
• an acid catalyst may be mixed with a mixed solution of thiol and a ketone or aldehyde, or a mixed solution of thiol and a ketone or aldehyde in the acid catalyst.
• a mixed solution of thiol and a ketone or aldehyde with an acid catalyst. Further, it is more preferable to supply the acid catalyst and the aromatic alcohol to the reaction vessel, and then supply the mixed solution of the thiol to the ketone or aldehyde to the reaction vessel for mixing.
• organic solvent In the production of bisphenol, an organic solvent is usually used to dissolve or disperse the produced bisphenol.
• the organic solvent is not particularly limited as long as it does not inhibit the reaction for producing bisphenol C, and examples thereof include aromatic hydrocarbons, aliphatic alcohols, and aliphatic hydrocarbons.
• aromatic hydrocarbons aliphatic alcohols
• aliphatic hydrocarbons aliphatic hydrocarbons.
• the aromatic alcohol as a substrate and the bisphenol as a product are removed from the organic solvent.
• These solvents may be used alone or in combination of two or more.
• aromatic hydrocarbons examples include benzene, toluene, xylene, ethylbenzene, diethylbenzene, isopropylbenzene, and mesitylene. These solvents may be used alone or in combination of two or more. After using the aromatic hydrocarbon for the production of bisphenol, it can be recovered and purified by distillation or the like and reused. When reusing aromatic hydrocarbons, those having a low boiling point are preferable. One of the preferred aromatic hydrocarbons is toluene.
• the aliphatic alcohol is an alkyl alcohol in which an alkyl group and a hydroxyl group are bonded.
• the fatty alcohol may be a monohydric aliphatic alcohol in which an alkyl group and one hydroxyl group are bonded, or may be a polyhydric aliphatic alcohol in which an alkyl group and two or more hydroxyl groups are bonded.
• the alkyl group may be linear, branched, unsubstituted, or partially substituted with an oxygen atom in the carbon atom of the alkyl group.
• the lipophilicity of the aliphatic alcohol increases as the number of carbon atoms increases, and it becomes difficult to mix with sulfuric acid and it becomes difficult to generate monoalkyl sulfate, which will be described later. More preferred.
• the aliphatic alcohol is preferably an alcohol in which an alkyl group and one hydroxyl group are bonded, and more preferably an alcohol in which an alkyl group having 1 to 8 carbon atoms and one hydroxyl group are bonded. More preferably, it is an alcohol in which 1 to 5 alkyl groups and 1 hydroxyl group are bonded.
• Specific aliphatic alcohols include, for example, methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol, t-butanol, n-pentanol, i-pentanol, n-hexanol, n. -Heptanol, n-octanol, n-nonanol, n-decanol, n-undecanol, n-dodecanol, ethylene glycol, diethylene glycol, triethylene glycol and the like can be mentioned.
• One of the preferred aliphatic alcohols is methanol.
• Aliphatic hydrocarbons include linear hydrocarbons having 5 to 18 carbon atoms such as n-pentane, n-hexane, n-heptane, and n-octane, and branched chain hydrocarbons having 5 to 18 carbon atoms such as isooctane. , Cyclohexane, cyclooctane, methylcyclohexane and other cyclic hydrocarbons having 5 to 18 carbon atoms.
• the mass ratio of the organic solvent to the ketone or aldehyde used for condensation ((mass of ketone / mass of organic solvent) or (mass of aldehyde / mass of organic solvent)) is too large, the ketone or aldehyde and the aromatic alcohol Is difficult to react and it takes a long time to react. If this mass ratio is too small, the increase in the amount of ketones or aldehydes is promoted, and the bisphenol produced may solidify. From these facts, the mass ratio of the organic solvent to the ketone or aldehyde at the time of preparation is preferably 0.5 or more, more preferably 1 or more, while preferably 100 or less, and more preferably 50 or less.
• Bisphenol is less likely to decompose if the generated bisphenol is dispersed without being completely dissolved in an organic solvent. It is preferable to use a solvent having a low solubility of bisphenol because the loss when recovering bisphenol from the reaction solution after the reaction is completed (for example, the loss to the filtrate during crystallization) can be reduced.
• the solvent having low solubility of bisphenol include aromatic hydrocarbons. Therefore, the organic solvent preferably contains aromatic hydrocarbons as a main component, preferably contains 55% by mass or more of aromatic hydrocarbons in the organic solvent, more preferably 70% by mass or more, and more preferably 80% by mass. It is more preferable to contain% or more.
• the organic solvent contains an aliphatic alcohol, so that the sulfuric acid reacts with the aliphatic alcohol to produce monoalkyl sulfate, and the effect that the catalytic action can also be obtained by this monoalkyl sulfate. Is obtained. Therefore, when the acid catalyst contains sulfuric acid, the organic solvent is preferably an organic solvent containing an aliphatic alcohol. As the aliphatic alcohol has a large number of carbon atoms, lipophilicity increases, it becomes difficult to mix with sulfuric acid, and it becomes difficult to generate monoalkyl sulfate. Therefore, an alkyl alcohol having 8 or less carbon atoms is preferable.
• the molar ratio of the aliphatic alcohol to sulfuric acid is preferably 0.01 or more, more preferably 0.05 or more, still more preferably 0.1 or more, preferably 10 or less, more preferably 5 or less. More preferably, it is 3 or less.
• the organic solvent can include, for example, aromatic hydrocarbons and aliphatic alcohols.
• the organic solvent may contain 1 to 95% by mass of aromatic hydrocarbons and 0.1 to 10% by mass of an aliphatic alcohol.
• the method for preparing the reaction solution is not particularly limited, and a method of supplying an acid catalyst to a mixed solution of a mixture of an aromatic alcohol, an organic solvent, a ketone or an aldehyde, or a method of mixing an acid catalyst, an aromatic alcohol and an organic solvent. Examples thereof include a method of supplying a ketone or an aldehyde to the mixed solution.
• the solution containing the ketone or aldehyde may contain the ketone or aldehyde alone, or may contain a thiol or an organic solvent.
• the solution containing a ketone or aldehyde preferably contains a thiol.
• reaction condition The reaction for producing bisphenol C is a condensation reaction. If the reaction temperature of the production reaction is too high, oxidative decomposition of thiol proceeds, and if it is too low, the time required for the reaction becomes long. Therefore, the reaction temperature is preferably 0 ° C. or higher and 50 ° C. or lower.
• the reaction time of the production reaction is preferably 30 hours or less, more preferably 25 hours or less, still more preferably 20 hours or less because the produced bisphenol is decomposed if it is too long.
• the lower limit of the reaction time is usually 0.5 hours or more. It is possible to stop the reaction by adding water equal to or more than the amount of sulfuric acid used or an aqueous sodium hydroxide solution so that the sulfuric acid concentration is 45% by mass or less to reduce the sulfuric acid concentration.
• Purification of the bisphenol C product obtained by the bisphenol C production reaction can be carried out by a conventional method. For example, it can be purified by a simple means such as crystallization or column chromatography. Specifically, after the condensation reaction, the organic phase obtained by separating the reaction solution is washed with water or saline, and if necessary, neutralized and washed with sodium bicarbonate water or the like. The washed organic phase is then cooled and crystallized. When a large amount of aromatic alcohol is used, excess aromatic alcohol by distillation is distilled off before crystallization and then crystallization is performed.
• trimethylbisphenol A produced as a by-product in the bisphenol C production reaction system remains, and a bisphenol C product containing trimethylbisphenol A is obtained as the bisphenol composition of the present invention. Therefore, in the above method for purifying a bisphenol C product, for example, crystallization, suspension washing, sprinkling washing and the like are appropriately combined to leave a predetermined amount of trimethylbisphenol A in the purified bisphenol C product. It is preferable to adjust the purification conditions so as to.
• Example of purification process As an example of a purification step suitable for the present invention, a method of purifying the bisphenol C product obtained by the condensation reaction after washing in the washing step and then precipitating in the crystallization step will be described below.
• the organic phase containing bisphenol C obtained from the reaction solution is washed with desalted water, and the washed organic phase is cooled and crystallized. Wash multiple times as follows. Crystallization may also be performed a plurality of times.
• First step After mixing the organic phase (O1) containing bisphenol C obtained from the reaction step and desalinated water, the organic phase (O2) containing bisphenol C and the aqueous phase (W1) are phase-separated. The aqueous phase (W1) is removed to obtain an organic phase (O2) containing bisphenol C.
• Second step After mixing the bisphenol C-containing organic phase (O2) obtained in the first water washing step with desalted water, the phase is separated into the bisphenol C-containing organic phase (O3) and the aqueous phase (W2). The aqueous phase (W2) is removed to obtain an organic phase (O3) containing bisphenol C.
• the first step is preferably performed so that the pH of the aqueous phase (W1) is 8.5 or higher.
• the second step is preferably performed so that the electrical conductivity of the aqueous phase (W2) is 10 ⁇ S / cm.
• the demineralized water is water that has undergone ion exchange treatment, pure water, or the like and has an electric conductivity of 1.5 ⁇ S / cm or less.
• the measurement temperature of the aqueous phase (W1) is preferably room temperature (20 to 30 ° C.), for example 25 ° C.
• the pH of the aqueous phase is lower than 7, it is possible to wash with a basic substance such as sodium hydroxide or sodium hydrogen carbonate, and then wash again with water.
• the organic phase obtained after washing with a basic substance is washed again with water so that the pH of the aqueous phase becomes 8.5 or higher.
• the pH is preferably 8.5 or higher, more preferably 9 or higher.
• the upper limit of the pH of the aqueous phase (W1) is usually. It is 14 or less, preferably 13 or less, and more preferably 12 or less.
• the measurement temperature of the electric conductivity of the aqueous phase (W2) in the second washing step is preferably room temperature (20 to 30 ° C.), for example 25 ° C.
• the electrical conductivity of the aqueous phase (W2) in the second washing step is preferably 10 ⁇ S / cm or less, more preferably 9 ⁇ S / cm or less, still more preferably 8 ⁇ S / cm or less.
• the organic phase containing bisphenol C was washed with water to make the pH of the obtained aqueous phase basic at pH 8.5 or higher, and then repeated washing with water as necessary to conduct electrical conduction of the obtained aqueous phase.
• the degree is 10 ⁇ S / cm or less, it is preferable to perform the crystallization step.
• acidic thionium is produced from the thiol, which is contained in the bisphenol composition and inhibits the polymerization reaction during the production of the polycarbonate resin.
• the aqueous phase (W1) ) And the electrical conductivity of the aqueous phase (W2) are controlled, so that thionium can be efficiently removed and polymerization inhibition by thionium can be prevented.
• the temperature in the washing step is 90 ° C. or lower, particularly 85 ° C. or lower, 50 ° C. or higher, particularly so that bisphenol can be efficiently precipitated by cooling in the crystallization step described later without evaporating the solvent. It is preferably 55 ° C. or higher.
• One washing time time for adding desalted water to the organic phase and mixing is usually about 1 to 120 minutes.
• the cooling temperature in the crystallization step should be 10 to 120 ° C. lower than the temperature of the organic phase (O3) obtained from the washing step, 40 ° C. or lower, particularly 30 ° C. or lower, -20 ° C. or higher, and particularly -10 ° C. or higher. Is preferable.
• the bisphenol composition precipitated in the crystallization step can be recovered by solid-liquid separation by filtration, centrifugation, decantation, or the like.
• the bisphenol composition of the present invention is a polyether resin, polyester resin, polyarylate resin, polycarbonate resin, polyurethane used for various purposes such as optical materials, recording materials, insulating materials, transparent materials, electronic materials, adhesive materials, and heat resistant materials.
• Components, curing agents, additives or their components such as various thermoplastic resins such as resins and acrylic resins, and various thermosetting resins such as epoxy resins, unsaturated polyester resins, phenol resins, polybenzoxazine resins and cyanate resins. It can be used as a precursor or the like.
• the bisphenol composition of the present invention is also useful as an additive such as a color developer such as a heat-sensitive recording material, a fading inhibitor, a bactericide, and an antibacterial and antifungal agent.
• the bisphenol composition of the present invention is preferably used as a raw material (monomer) for a thermoplastic resin and a thermosetting resin because it can impart good mechanical properties, and more particularly as a raw material for a polycarbonate resin and an epoxy resin. preferable.
• the bisphenol composition of the present invention is also preferably used as a color developer, and more preferably used in combination with a leuco dye and a discoloration temperature adjuster.
• the polycarbonate resin of the present invention is a polycarbonate resin having at least a repeating structural unit represented by the following general formula (A), and is a compound obtained by alkaline hydrolysis of the polycarbonate resin (hereinafter, "alkaline water addition").
• composition product is a polycarbonate containing bisphenol (I) and bisphenol (II), and the amount of bisphenol (II) obtained by alkaline hydrolysis is 160% by mass or more with respect to the polycarbonate resin.
• Such a polycarbonate resin of the present invention can be produced by using the bisphenol composition of the present invention.
• R 1 to R 6 are synonymous with those in the general formula (1).
• the ratio of this bisphenol (II) to the polycarbonate resin is preferably 200 mass ppm or more, more preferably 300 mass ppm or more, preferably 20000 mass ppm or less, and more preferably 15000 mass ppm or less.
• the bisphenol composition of the present invention and diphenyl carbonate or the like are used in the presence of an alkali metal compound and / or an alkaline earth metal compound. Examples thereof include a method of transesterifying.
• the bisphenol composition of the present invention may contain only one type of bisphenol (I), and may contain two or more types of bisphenol (I), or one or more types of bisphenol (I) and other bisphenols. It may be included.
• a copolymerized polycarbonate resin can be produced by using two or more kinds of bisphenols. Further, a dihydroxy compound other than the bisphenol composition of the present invention can be used in combination for reaction.
• the transesterification reaction can be carried out by appropriately selecting a known method.
• An example of a method for producing a polycarbonate resin using the bisphenol composition of the present invention and diphenyl carbonate as raw materials will be described below.
• diphenyl carbonate in an excess amount with respect to the bisphenol in the bisphenol composition of the present invention.
• the amount of diphenyl carbonate used for bisphenol is preferably large in that the produced polycarbonate resin has few terminal hydroxyl groups and is excellent in thermal stability of the polymer.
• the amount of diphenyl carbonate used for bisphenol is preferably small in that the transesterification reaction rate is high and a polycarbonate resin having a desired molecular weight can be easily produced. From these facts, the amount of diphenyl carbonate used with respect to 1 mol of bisphenol is usually 1.001 mol or more, preferably 1.002 mol or more, and usually 1.3 mol or less, preferably 1.2 mol or less.
• the bisphenol composition and diphenyl carbonate of the present invention can be supplied as a solid, but it is preferable to melt one or both of them and supply them in a liquid state.
• a transesterification catalyst When producing a polycarbonate resin by transesterification reaction of diphenyl carbonate and bisphenol, a transesterification catalyst is usually used.
• a transesterification catalyst In the above method for producing a polycarbonate resin, it is preferable to use an alkali metal compound and / or an alkaline earth metal compound as the transesterification catalyst. These may be used alone or in combination of two or more in any combination and ratio. Practically, it is desirable to use an alkali metal compound.
• the amount of the catalyst used is usually 0.05 ⁇ mol or more, preferably 0.08 ⁇ mol or more, more preferably 0.10 ⁇ mol or more, and usually 100 ⁇ mol or less, preferably 50 ⁇ mol, based on 1 mol of bisphenol or diphenyl carbonate. Below, it is more preferably 20 ⁇ mol or less.
• the amount of the catalyst used is within the above range, the polymerization activity required for producing a polycarbonate resin having a desired molecular weight can be easily obtained, the polymer hue is excellent, and excessive polymer branching does not proceed. It is easy to obtain a polycarbonate resin with excellent fluidity during molding.
• both of the above raw materials are continuously supplied to the raw material mixing tank, and the obtained mixture and the transesterification catalyst are continuously supplied to the polymerization tank.
• both raw materials supplied to the raw material mixing tank are usually stirred uniformly and then supplied to a polymerization tank to which a transesterification catalyst is added to produce a polymer.
• the polymerization reaction temperature is preferably 80 ° C. or higher, particularly 150 ° C. or higher, 400 ° C. or lower, particularly 350 ° C. or lower.
• the polymerization time is appropriately adjusted depending on the ratio of raw materials, the desired molecular weight of the polycarbonate resin, and the like. If the polymerization time is long, quality deterioration such as color tone deterioration becomes apparent. Therefore, it is preferably 10 hours or less, and more preferably 8 hours or less.
• the lower limit of the polymerization time is usually 0.1 hours or more, or 0.3 hours or more.
• a polycarbonate resin having a good hue and excellent transparency it is possible to produce a polycarbonate resin having a good hue and excellent transparency.
• a polycarbonate resin having a viscosity average molecular weight (Mv) of 10,000 or more, preferably 15,000 or more, 100,000 or less, preferably 35,000 or less, and a pellet YI of 10 or less, which has a good hue and excellent transparency can be produced in a short time. ..
• composition analysis of bisphenol C production reaction solution, trimethylbisphenol A analysis in bisphenol C composition, trimethylbisphenol A analysis in alkali hydrolysis product of polycarbonate resin is performed by high performance liquid chromatography under the following procedure and conditions. It was.
• LCMS high performance liquid chromatography mass spectrometry
• LCMS High Performance Liquid Chromatography Mass Spectrometry
• ⁇ Analysis of bisphenol C in bisphenol C composition> The analysis of bisphenol C in the bisphenol C composition is the same as ⁇ composition of bisphenol C production reaction solution, trimethylbisphenol A analysis in bisphenol C composition, trimethylbisphenol A analysis in alkali hydrolysis product of polycarbonate resin>. Carried out.
• the purity of bisphenol C in bisphenol in the bisphenol C composition produced in the present invention is usually 99% by mass or more, and the amount of bisphenol other than bisphenol C produced is very small. Therefore, bisphenol C in the bisphenol C composition
• the content can be regarded as the bisphenol content.
• ⁇ Methanol-dissolved color of bisphenol C composition The color of the bisphenol C composition dissolved in methanol is determined by adding 10 g of the bisphenol C composition and 10 g of methanol to a test tube "P-24" (24 mm ⁇ x 200 mm) manufactured by Niommen Rika Glass Co., Ltd. to make a homogeneous solution, and then at room temperature (about 20). The number of Hazen colors was measured and evaluated using "SE6000" manufactured by Nippon Denshoku Kogyo Co., Ltd. at (° C.).
• the melt color difference of the bisphenol C composition is as follows: 20 g of the bisphenol C composition is placed in a test tube "P-24" (24 mm ⁇ x 200 mm) manufactured by Niommen Rika Glass Co., Ltd., melted at 190 ° C. for 30 minutes, and manufactured by Nippon Denshoku Kogyo Co., Ltd. Using "SE6000", the number of Hazen colors was measured and evaluated.
• Thermal color stability of bisphenol C composition For the thermal color stability of the bisphenol C composition, 20 g of the bisphenol C composition was placed in a test tube "P-24" (24 mm ⁇ x 200 mm) manufactured by Niommen Rika Glass Co., Ltd. and melted at 190 ° C. for 4 hours. The number of Hazen colors was measured and evaluated using "SE6000" manufactured by Japan.
• ⁇ Pyrolysis stability of bisphenol C composition For the thermal decomposition stability of the bisphenol C composition, 20 g of the bisphenol C composition was placed in a test tube "P-24" (24 mm ⁇ x 200 mm) manufactured by Niommen Rika Glass Co., Ltd. and melted at 190 ° C. for 2 hours to produce the bisphenol C formation reaction. It was carried out in the same manner as the composition analysis of the liquid, and the amount of isopropenyl cresol produced was measured and evaluated.
• CM-A212 for petri dish measurement was fitted into the measuring section, and the zero calibration box “CM-A124" was placed over it to perform zero calibration, and then white calibration was performed using the built-in white calibration plate. ..
• CM-A210 white calibration plate
• L * was 99.40 ⁇ 0.05
• a * was 0.03 ⁇ 0.01
• b * was -0.43 ⁇ 0.01.
• YI was confirmed to be ⁇ 0.58 ⁇ 0.01.
• YI was measured by packing pellets to a depth of about 40 mm in a cylindrical glass container having an inner diameter of 30 mm and a height of 50 mm. The operation of taking out the pellets from the glass container and then performing the measurement again was repeated twice, and the average value of the measured values of a total of three times was used.
• Example 1 (1) Preparation of the first mixed solution In a separable flask equipped with a thermometer, a dropping funnel, a jacket and an anchor-type stirring blade, 320 g of toluene, 15 g of methanol, and Fuji Film Wako Pure Chemical Industries, Ltd. (reagent) under a nitrogen atmosphere. ), 230 g (2.13 mol) of orthocresol was added, and the internal temperature was set to 10 ° C. or lower. Then, 95 g of 98 mass% sulfuric acid was slowly added over 0.3 hours with stirring, and then cooled to 5 ° C. or lower.
• reaction solution After the internal temperature of the first mixed solution is lowered to 5 ° C. or lower, the second mixed solution is subjected to the second mixed solution using the dropping funnel over 1 hour so that the internal temperature does not reach 10 ° C. or higher. And supplied to prepare a reaction solution.
• the obtained sixth organic phase was cooled from 80 ° C. to 20 ° C. and maintained at 20 ° C. to precipitate bisphenol C. Then, after cooling to 10 ° C. and reaching 10 ° C., solid-liquid separation was performed using a centrifuge to obtain a crudely purified wet cake. The obtained wet cake was washed by sprinkling 500 g of toluene, and solid-liquid separation was performed using a centrifuge to obtain a purified wet cake. The obtained refined wet cake was distilled off with a light boiling point at an oil bath temperature of 100 ° C. under reduced pressure using an evaporator equipped with an oil bath to obtain 190 g of a white bisphenol C composition.
• the number of Hazen colors was 0.
• the melt color difference of the obtained bisphenol C composition was measured, the number of Hazen colors was 3.
• the thermal color stability of the obtained bisphenol C composition was measured, the number of Hazen colors was 26.
• the thermal decomposition stability of the obtained bisphenol C composition was measured, the amount of isopropenyl cresol produced was 186 mass ppm.
• the obtained bisphenol C composition contained 210 mass ppm of trimethylbisphenol A.
• the bisphenol C content in the obtained bisphenol C composition was 99.9% by mass.
• Example 2 (1) Preparation of the first mixed solution In a separable flask equipped with a thermometer, a dropping funnel, a jacket and an anchor-type stirring blade, 320 g of toluene, 15 g of methanol, and 5 g of 2,6-xylenol (0.04) under an air atmosphere. (Mol) and 225 g (2.08 mol) of orthocresol manufactured by Fuji Film Wako Pure Chemical Industries, Ltd. (reagent) were added, and the internal temperature was set to 10 ° C. or lower. Then, 95 g of 98 mass% sulfuric acid was slowly added over 0.3 hours with stirring, and then cooled to 5 ° C. or lower.
• reaction solution After the internal temperature of the first mixed solution is lowered to 5 ° C. or lower, the second mixed solution is subjected to the second mixed solution using the dropping funnel over 1 hour so that the internal temperature does not reach 10 ° C. or higher. And supplied to prepare a reaction solution.
• the obtained sixth organic phase was cooled from 80 ° C. to 20 ° C. and maintained at 20 ° C. to precipitate bisphenol C. Then, after cooling to 10 ° C. and reaching 10 ° C., solid-liquid separation was performed using a centrifuge to obtain a crudely purified wet cake. The obtained wet cake was washed by sprinkling 500 g of toluene, and solid-liquid separation was performed using a centrifuge to obtain a purified wet cake. The obtained refined wet cake was distilled off with a light boiling point at an oil bath temperature of 100 ° C. under reduced pressure using an evaporator equipped with an oil bath to obtain 178 g of a white bisphenol C composition.
• the bisphenol C content in the obtained bisphenol C composition was 99.7% by mass, and the trimethylbisphenol A content was 20000% by mass.
• the number of Hazen colors was 0.
• the melt color difference of the obtained bisphenol C composition was measured, the number of Hazen colors was 8.
• the thermal color stability of the obtained bisphenol C composition was measured, the number of Hazen colors was 32.
• the thermal decomposition stability of the obtained bisphenol C composition was measured, the amount of isopropenyl cresol produced was 166 mass ppm.
• reaction solution After the internal temperature of the first mixed solution is lowered to 5 ° C. or lower, the second mixed solution is subjected to the second mixed solution using the dropping funnel over 1 hour so that the internal temperature does not reach 10 ° C. or higher. And supplied to prepare a reaction solution.
• the obtained 7th organic phase was cooled from 80 ° C. to 20 ° C. and maintained at 20 ° C. to precipitate bisphenol C. Then, after cooling to 10 ° C. and reaching 10 ° C., solid-liquid separation was performed using a centrifuge to obtain a wet cake. The obtained wet cake was washed by sprinkling 200 g of toluene, and solid-liquid separation was performed using a centrifuge to obtain a purified wet cake. The obtained refined wet cake was distilled off with a light boiling point at an oil bath temperature of 100 ° C. under reduced pressure using an evaporator equipped with an oil bath to obtain 183 g of a white bisphenol C composition.
• the bisphenol C content in the obtained bisphenol C composition was 99.9% by mass, and trimethylbisphenol A was not detected (quantification limit was less than 0.1% by mass).
• the number of Hazen colors was 3.
• the melt color difference of the obtained bisphenol C composition was measured, the number of Hazen colors was 48.
• the thermal color stability of the obtained bisphenol C composition was measured, the number of Hazen colors was 120.
• the thermal decomposition stability of the obtained bisphenol C was measured, the amount of isopropenyl cresol produced was 485 mass ppm.
• reaction solution After the internal temperature of the first mixed solution is lowered to 5 ° C. or lower, the second mixed solution is subjected to the second mixed solution using the dropping funnel over 1 hour so that the internal temperature does not reach 10 ° C. or higher. And supplied to prepare a reaction solution.
• the obtained 7th organic phase was cooled from 80 ° C. to 20 ° C. and maintained at 20 ° C. to precipitate bisphenol C. Then, after cooling to 10 ° C. and reaching 10 ° C., solid-liquid separation was performed using a centrifuge to obtain a wet cake. The obtained wet cake was washed by sprinkling 200 g of toluene, and solid-liquid separation was performed using a centrifuge to obtain a purified wet cake. The obtained refined wet cake was distilled off with a light boiling point at an oil bath temperature of 100 ° C. under reduced pressure using an evaporator equipped with an oil bath to obtain 160 g of a white bisphenol C composition.
• the bisphenol C content in the obtained bisphenol C composition was 99.9% by mass, and the trimethylbisphenol A content was 55% by mass.
• the number of Hazen colors was 2.
• the melt color difference of the obtained bisphenol C composition was measured, the number of Hazen colors was 39.
• the thermal color stability of the obtained bisphenol C composition was measured, the number of Hazen colors was 105.
• the thermal decomposition stability of the obtained bisphenol C was measured, the amount of isopropenyl cresol produced was 412 mass ppm.
• Example 3 100.00 g (0.39 mol of bisphenol C) and 86.49 g (0.4) of diphenyl carbonate obtained in Example 1 in a glass reaction tank having an internal volume of 150 mL equipped with a stirrer and a distillate. Mol) and 479 ⁇ L of a 400 mass ppm cesium carbonate aqueous solution were added. The operation of reducing the pressure of the glass reaction vessel to about 100 Pa and then restoring the pressure to atmospheric pressure with nitrogen was repeated three times to replace the inside of the reaction vessel with nitrogen. Then, the reaction vessel was immersed in an oil bath at 200 ° C. to dissolve the contents.
• the rotation speed of the stirrer is set to 100 times per minute, and the pressure in the reaction vessel is adjusted to absolute pressure over 40 minutes while distilling off the phenol produced by the oligomerization reaction of bisphenol C and diphenyl carbonate in the reaction vessel.
• the pressure was reduced from 101.3 kPa to 13.3 kPa.
• the transesterification reaction was carried out for 80 minutes while maintaining the pressure in the reaction vessel at 13.3 kPa and further distilling off phenol.
• the temperature outside the reaction vessel was raised to 250 ° C., and the pressure inside the reaction vessel was reduced from 13.3 kPa to 399 Pa in absolute pressure over 40 minutes to remove the distilled phenol from the system.
• the temperature outside the reaction vessel was raised to 280 ° C.
• the absolute pressure in the reaction vessel was reduced to 30 Pa, and the polycondensation reaction was carried out.
• the polycondensation reaction was terminated when the stirrer in the reaction tank became a predetermined stirring power.
• the time from the temperature rise to 280 ° C. to the end of the polymerization was 210 minutes.
• the reaction vessel was repressurized to 101.3 kPa with nitrogen at an absolute pressure, and then the pressure was increased to 0.2 MPa with a gauge pressure, and the polycarbonate resin was extracted from the bottom of the reaction vessel in a strand shape to obtain a strand-shaped polycarbonate resin. .. Then, the strands were pelletized using a rotary cutter to obtain a pellet-shaped polycarbonate resin.
• the viscosity average molecular weight (Mv) of the obtained polycarbonate resin was 24,800, and the pellet YI was 6.9.
• the amount of trimethylbisphenol A in the alkali hydrolysis product of the obtained polycarbonate resin was 160 mass ppm with respect to the polycarbonate resin.
• Example 4 In Example 3, instead of 100.00 g (bisphenol C 0.39 mol) of the bisphenol C composition obtained in Example 1, 100.00 g (bisphenol C 0.39) of the bisphenol C composition obtained in Example 2 was used. It was carried out in the same manner as in Example 3 except that it was used. The time from the temperature rise to 280 ° C. to the end of the polymerization (post-stage polymerization time) was 220 minutes. The viscosity average molecular weight (Mv) of the obtained polycarbonate resin was 24,800, and the pellet YI was 6.5. The amount of trimethylbisphenol A in the alkali hydrolysis product of the obtained polycarbonate resin was 16200 mass ppm with respect to the polycarbonate resin.
• Example 3 In Example 3, instead of 100.00 g (bisphenol C 0.39 mol) of the bisphenol C composition obtained in Example 1, 100.00 g (bisphenol C 0.39) of the bisphenol C composition obtained in Comparative Example 1 was used. It was carried out in the same manner as in Example 3 except that it was used. The time from the temperature rise to 280 ° C. to the end of the polymerization (post-stage polymerization time) was 230 minutes. The viscosity average molecular weight (Mv) of the obtained polycarbonate resin was 24,800, and the pellet YI was 10.2. The amount of trimethylbisphenol A in the alkali hydrolysis product of the obtained polycarbonate resin was 2 mass ppm with respect to the polycarbonate resin.

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