Method for producing bisphenol and method for producing polycarbonate resin

Abstract

To provide a method for producing a bisphenol with excellent melting colors.SOLUTION: A method for producing a bisphenol includes a redox step for adding an oxidizer to a bisphenol solution and then adding a reductant.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to a method for producing bisphenol and a method for producing polycarbonate resin. [Background technology]

[0002] Bisphenols are useful as raw materials for polymeric materials such as polycarbonate resins, epoxy resins, aromatic polyester resins, etc. Representative bisphenols include, for example, 2,2-bis(4-hydroxyphenyl)propane and 2,2-bis(4-hydroxy-3-methylphenyl)propane (Patent Documents 1 and 2). [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Japanese Patent Application Laid-Open No. 62-138443 [Patent Document 2] JP 2008-214248 A Summary of the Invention [Problem to be solved by the invention]

[0004] Polycarbonate resin, a typical resin obtained by using bisphenol as a raw material, is required to be colorless and transparent. The color tone of polycarbonate resin is greatly affected by the color tone of the raw material. Therefore, the color tone of the raw material bisphenol is also required to be colorless. Here, since it is difficult to directly quantify the color of bisphenol powder, the color tone when dissolved in a solvent may be evaluated as the color tone of bisphenol. In this specification, this color tone is referred to as "melt color". In the production of polycarbonate resin, especially in the melting method, bisphenol is melted to produce polycarbonate resin, so it is exposed to high temperatures. Therefore, thermal color stability of bisphenol is also required. In addition, polycarbonate resins are required to have a designed molecular weight and good color tone, and therefore, for the production of such polycarbonate resins, bisphenols that are excellent in melt color are required as raw materials.

[0005] The present invention has been made in view of the above-mentioned conventional circumstances, and has an object to provide a method for producing bisphenol which has a good melt color. [Means for solving the problem]

[0006] As a result of intensive research aimed at solving the above problems, the inventors discovered that the melt color of bisphenol can be improved by reacting bisphenol with an oxidizing agent and then with a reducing agent, thereby completing the present invention.

[0007] That is, the gist of the present invention lies in the following [1] to [7]. [1] A method for producing bisphenol, comprising the steps of: A method for producing bisphenol, comprising an oxidation-reduction step of adding an oxidizing agent to a bisphenol solution and then adding a reducing agent. [2] The bisphenol solution is The method for producing bisphenol according to [1], wherein the solution is obtained by a reaction step in which a ketone or an aldehyde is subjected to a condensation reaction with an aromatic alcohol in the presence of an acidic catalyst, followed by a neutralization step in which an organic layer of the reaction solution obtained in the reaction step is neutralized. [3] The bisphenol solution is The method for producing bisphenol according to [1], wherein the solution is obtained by dissolving a bisphenol composition in an organic solvent. [4] The method for producing bisphenol according to [2], wherein the ketone or aldehyde is acetone or acetaldehyde. [5] The method for producing bisphenol according to [2], wherein the ketone or aldehyde is a ketone. [6] The method for producing bisphenol according to any one of [1] to [5], wherein the bisphenol is 2,2-bis(4-hydroxy-3-methylphenyl)propane. [7] A method for producing a polycarbonate resin, comprising a step of polymerizing a polycarbonate resin using, as a raw material, a bisphenol produced by the method for producing bisphenol according to any one of [1] to [6]. Effect of the Invention

[0008] According to the present invention, a method for producing bisphenol with good melt color is provided by reacting an oxidizing agent and then a reducing agent, and a method for producing polycarbonate resin using this bisphenol provides polycarbonate resin with excellent color tone. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] The following describes the embodiments of the present invention in detail, but the following description of the constituent elements is one example (representative example) of the embodiment of the present invention, and the present invention is not limited to the following content as long as the gist of the present invention is not changed. Note that when the expression "~" is used in this specification, it is used as an expression including the numerical values ​​or physical property values ​​before and after it.

[0010] <1. Manufacturing method of bisphenol> A method for producing bisphenol according to one embodiment of the present invention (hereinafter also simply referred to as a "method for producing bisphenol") is a method for producing bisphenol, which includes an oxidation-reduction step of adding an oxidizing agent to a bisphenol solution and then adding a reducing agent. The method for producing bisphenol according to this embodiment may include a step other than the above-mentioned oxidation-reduction step.

[0011] The bisphenol obtained by the above-mentioned production method has a good melt color. In this specification, the "melt color" is an index for evaluating the color tone of the bisphenol, and can evaluate the color tone of a solution obtained by heating and melting the bisphenol. The present inventors consider the reason why the above-mentioned effect is obtained by the method for producing bisphenol according to the present embodiment as follows. As a result of intensive research by the present inventors, it was found that the cause of the deterioration in color tone is a component (a component causing deterioration in color tone) that is generated by oxidation with an oxidizing agent and then reduction with a reducing agent, and that is contained in the aqueous phase when the organic phase and the aqueous phase are separated. The present inventors then found that by adding an oxidizing agent and then a reducing agent to a bisphenol solution, the amount of the component causing deterioration in color tone in the solution can be reduced, that is, bisphenol with good color tone can be produced.

[0012] The bisphenol solution is not particularly limited, but from the viewpoint of the stability of the oxidizing agent or reducing agent against pH, it may be a solution obtained by a neutralization process in which an organic layer of the reaction liquid obtained by a reaction process in which a ketone or aldehyde is subjected to a condensation reaction with an aromatic alcohol in the presence of an acidic catalyst to produce the bisphenol solution (hereinafter, also referred to as a "first bisphenol solution"), and from the viewpoint that in a solid state, only the surface is affected and sufficient effect cannot be obtained, it is preferable that the bisphenol solution is a solution obtained by dissolving a bisphenol composition in an organic solvent (hereinafter, also referred to as a "second bisphenol solution").

[0013] <1-1. First bisphenol solution> The following describes the case where the bisphenol solution is a first bisphenol solution, that is, a solution obtained by a reaction step in which a ketone or aldehyde and an aromatic alcohol are subjected to a condensation reaction in the presence of an acidic catalyst to produce a bisphenol solution, followed by a neutralization step in which the organic layer of the reaction solution obtained by the reaction step is neutralized.

[0014] <1-1-1. Reaction process> The first method for producing a bisphenol solution (hereinafter also referred to as the "method for producing bisphenol according to this embodiment" in this section) has a reaction step of producing bisphenol by a condensation reaction of acetone or an aldehyde with an aromatic alcohol in the presence of an acidic catalyst to obtain a bisphenol solution.

[0015] [Aromatic alcohols] The aromatic alcohol used in the method for producing bisphenol according to this embodiment is not particularly limited, but is usually a compound represented by the following general formula (1). [ka]

[0016] R 1 ~R 4 are each independently a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an aryl group, etc. The alkyl group, the alkoxy group, the aryl group, etc. may be substituted or unsubstituted. For example, a hydrogen atom, a fluoro group, a chloro group, a bromo group, an iodo group, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, an n-pentyl group, an i-pentyl group, an n-hexyl group, an n-heptyl group, an n-octyl group, an n-nonyl group, an n-decyl group, an n-undecyl group, an n-dodecyl group, a methoxy group, an ethoxy group, an n-propoxy group, an i-propoxy group, an n-butoxy group, an i-butoxy group, a t-butoxy group, etc. Examples of such groups include an n-pentyloxy group, an i-pentyloxy group, an n-hexyloxy group, an n-heptyloxy group, an n-octyloxy group, an n-nonyloxy group, an n-decyloxy group, an n-undecyloxy group, an n-dodecyloxy group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cyclododecyl group, a benzyl group, a phenyl group, a tolyl group, and a 2,6-dimethylphenyl group.

[0017] Of these, R 2 and R 3 is preferably a hydrogen atom since the condensation reaction is difficult to proceed if it is sterically bulky. 1 and R 4 are each independently preferably a hydrogen atom, an alkyl group, an alkoxy group, an aryl group, or an amino group, and more preferably a hydrogen atom or an alkyl group. 1 and R4 are each independently a hydrogen atom or an alkyl group, and R 2 and R 3 is a hydrogen atom. The alkyl group may be an alkyl group having 1 to 12 carbon atoms or an alkyl group having 1 to 6 carbon atoms.

[0018] Specific examples of the compound represented by the above general formula (1) include phenol, cresol, xylenol, ethylphenol, propylphenol, butylphenol, methoxyphenol, ethoxyphenol, propoxyphenol, butoxyphenol, aminophenol, benzylphenyl, and phenylphenol.

[0019] Among them, the aromatic alcohol is preferably one other than xylenol, is preferably any one selected from the group consisting of phenol and cresol, and is more preferably cresol. The aromatic alcohols may be used alone or in any combination of two or more in any ratio.

[0020] [Ketone or aldehyde] The ketone or aldehyde used in the method for producing bisphenol according to this embodiment is not particularly limited, but is usually a compound represented by the following general formula (2). [ka]

[0021] R 5 and R 6are each independently a hydrogen atom, an alkyl group, an alkoxy group, an aryl group, etc. The alkyl group, alkoxy group, aryl group, etc. may be substituted or unsubstituted. For example, a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, an n-pentyl group, an i-pentyl group, an n-hexyl group, an n-heptyl group, an n-octyl group, a 2-ethylhexyl group, an n-nonyl group, an n-decyl group, an n-undecyl group, an n-dodecyl group, a methoxy group, an ethoxy group, an n-propoxy group, an i-propoxy group, an n-butoxy group, an i-butoxy group, a t-butoxy group, an n-pentyl group, an i ... Examples of such aryloxy groups include butyloxy, isobutyloxy, n-hexyloxy, n-heptyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, n-undecyloxy, n-dodecyloxy, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclododecyl, benzyl, phenyl, tolyl, and 2,6-dimethylphenyl groups. The present inventors have found that the components causing the deterioration of color tone are some of the components derived from aldehydes that are separated into the aqueous phase by the addition of an oxidizing agent and a reducing agent. Therefore, the ketone or aldehyde used in the method for producing bisphenol according to the present embodiment is preferably a ketone since it is preferable that the content of aldehydes that can generate the components causing the deterioration of color tone is low. Specifically, 5 and R 6 is preferably a group other than a hydrogen atom. Note that the color tone deteriorating components do not correspond to all compounds generated from aldehydes, but rather to some of the compounds that can be generated from aldehydes.

[0022] R 5 and R 6 may be bonded or bridged to each other between the two groups, R 5 and R 6 and may be bonded together with adjacent carbon atoms to form a cycloalkylidene group, which is a divalent group formed by removing two hydrogen atoms from one carbon atom of a cycloalkane. R 5 and R 6 Examples of the cycloalkylidene group formed by bonding together with adjacent carbon atoms include cyclopropylidene, cyclobutylidene, cyclopentylidene, cyclohexylidene, 3,3,5-trimethylcyclohexylidene, cycloheptylidene, cyclooctylidene, cyclononylidene, cyclodecylidene, cycloundecylidene, cyclododecylidene, fluorenylidene, xanthonylidene, and thioxanthonylidene.

[0023] Specific examples of the compound represented by the above general formula (2) include formaldehyde, acetaldehyde, Aldehydes such as aldehyde, propionaldehyde, butyraldehyde, pentanaldehyde, hexanealdehyde, heptanealdehyde, octananealdehyde, nonanaldehyde, decananealdehyde, undecanealdehyde, and dodecanealdehyde; ketones such as acetone, butanone, pentanone, hexanone, heptanone, octanone, nonanone, decanone, undecanone, and dodecanone; benzaldehyde, phenyl methyl ketone, phenyl ethyl ketone, and Examples of the aldehyde include acetaldehyde, aryl alkyl ketones such as phenyl propyl ketone, cresyl methyl ketone, cresyl ethyl ketone, cresyl propyl ketone, xylyl methyl ketone, xylyl ethyl ketone, and xylyl propyl ketone, and cyclic alkane ketones such as cyclopropanone, cyclobutanone, cyclopentanone, cyclohexanone, cycloheptanone, cyclooctanone, cyclononanone, cyclodecanone, cycloundecanone, and cyclododecanone. The aldehyde is preferably acetaldehyde, and the ketone is preferably acetone, and it is particularly preferable to use acetone. The ketones or aldehydes may be used alone or in any combination of two or more in any ratio.

[0024] By using a ketone with a low aldehyde content, a bisphenol having a good melt color can be produced. In addition, a polycarbonate resin having an excellent color tone can be produced by using the obtained bisphenol. The aldehyde content in the ketone is usually 300 mass ppm or less, preferably 200 mass ppm or less, more preferably 150 mass ppm or less, and further preferably 100 mass ppm or less, and the lower limit is not particularly limited, but is usually 0.1 mass ppm or more, may be 0.2 mass ppm or more, and may be 0.3 mass ppm or more. The aldehyde content in the ketone can be quantified, for example, by gas chromatography. In this specification, unless otherwise specified, "mass" refers to the mass of a single type of target element when the target element is composed of a single type, and refers to the total mass of the multiple types of target elements when the target element is composed of multiple types.

[0025] Ketones that satisfy the above range of aldehyde content may be obtained by commercially available ketones with low aldehyde content, or by subjecting ketones with high aldehyde content to a treatment for removing aldehydes. The treatment for removing aldehydes from ketones may be carried out by applying a known method, for example, by distillation after chemical treatment (oxidation or reduction).

[0026] When the amount of ketone or aldehyde is large relative to the aromatic alcohol as a raw material, the ketone or aldehyde is likely to polymerize, and when the amount is small, the aromatic alcohol is lost unreacted. For these reasons, the molar ratio of aromatic alcohol to ketone or aldehyde (moles of aromatic alcohol / moles of ketone or aldehyde) is preferably 1.5 or more, more preferably 1.6 or more, and even more preferably 1.7 or more, and is preferably 15 or less, more preferably 10 or less, and even more preferably 8 or less.

[0027] [Acidic catalyst] The type of acid catalyst used in the bisphenol production method according to this embodiment is not particularly limited, and examples thereof that can be used include sulfuric acid, hydrochloric acid, hydrogen chloride gas, phosphoric acid, aromatic sulfonic acids such as p-toluenesulfonic acid, and aliphatic sulfonic acids such as methanesulfonic acid. From the viewpoints of reactivity and economy, however, sulfuric acid or hydrochloric acid is preferred.

[0028] If the molar ratio of the acid catalyst to the ketone or aldehyde used in the condensation (moles of acid catalyst / moles of ketone or aldehyde) is low, the acid catalyst is diluted by the by-product water as the condensation reaction proceeds, and the reaction takes time. In view of the above, the molar ratio of the acid catalyst to the ketone or aldehyde used in the condensation is preferably 0.01 or more, more preferably 0.05 or more, and even more preferably 0.1 or more, and is preferably 10 or less, more preferably 8 or less, and even more preferably 5 or less.

[0029] [Thiol cocatalyst] In the method for producing bisphenol according to the present embodiment, a thiol promoter can be used as a promoter in the reaction of condensing a ketone or an aldehyde with an aromatic alcohol. Examples of the thiol promoter used as a promoter 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, butyl mercaptan, pentyl mercaptan, hexyl mercaptan, heptyl mercaptan, octyl mercaptan, nonyl mercaptan, decyl mercaptan (decanethiol), undecyl mercaptan (undecanethiol), dodecyl mercaptan (dodecanethiol), Examples of suitable alkyl thiols include tridecyl mercaptan, tetradecyl mercaptan, pentadecyl mercaptan, mercaptophenol, and the like. However, since mercaptocarboxylic acids are highly hydrophilic and therefore difficult to mix with bisphenol raw materials, alkyl thiols are preferred. As alkyl thiols, those with 6 or more carbon atoms are preferred because smaller alkyl groups have lower boiling points and are difficult to handle (odor). In particular, dodecyl mercaptan (dodecanethiol) is preferred from the viewpoints of availability, lipophilicity, high boiling point, and ease of handling.

[0030] When the molar ratio of the thiol promoter to the ketone or aldehyde used in the condensation (the number of moles of the thiol promoter / the number of moles of the ketone or aldehyde) is low, it is difficult to obtain the effect of improving the reaction selectivity of bisphenol by using the thiol promoter. Note that the reaction selectivity of bisphenol is an index of the ease with which the target bisphenol is produced in the production reaction of bisphenol, and the more excellent the reaction selectivity of bisphenol is, the greater the amount of bisphenol produced. In addition, if the molar ratio of the thiol promoter to the ketone or aldehyde used in the condensation is high, it may be mixed into the bisphenol and deteriorate the quality. For these reasons, the molar ratio of the thiol promoter to the ketone or aldehyde is preferably 0.001 or more, more preferably 0.005 or more, even more preferably 0.01 or more, and is preferably 1 or less, more preferably 0.5 or less, even more preferably 0.1 or less.

[0031] As described later, it is preferable that the thiol promoter is mixed with the ketone or aldehyde beforehand and then used for the reaction. The method of mixing the thiol promoter and the ketone or aldehyde may be to supply the ketone or aldehyde to the thiol promoter, or the thiol promoter may be supplied to the ketone or aldehyde. The method of mixing the mixed solution of the thiol promoter and the ketone or aldehyde with the acid catalyst may be to supply the acid catalyst to the mixed solution of the thiol promoter and the ketone or aldehyde, or the mixed solution of the thiol promoter and the ketone or aldehyde to the acid catalyst. In order to suppress the self-condensation of the ketone or aldehyde, it is preferable to supply the mixed solution of the thiol promoter and the ketone or aldehyde to the acid catalyst. Furthermore, it is more preferable to supply the mixed solution of the thiol promoter and the ketone or aldehyde to the acid catalyst after supplying the acid catalyst and aromatic alcohol to the reaction vessel and then supplying the mixed solution of the thiol promoter and the ketone or aldehyde to the reaction vessel to mix them.

[0032] [Reaction solvent] In the method for producing bisphenol according to the present embodiment, the condensation reaction between aromatic alcohol and ketone or aldehyde may be carried out in the presence of a solvent. The solvent is not particularly limited as long as it does not inhibit the reaction for producing bisphenol, and examples of the solvent include aromatic hydrocarbons, aliphatic alcohols, and aliphatic hydrocarbons. These solvents may be used alone or in combination of two or more. Good too.

[0033] Examples of aromatic hydrocarbons include benzene, toluene, xylene, ethylbenzene, diethylbenzene, isopropylbenzene, and mesitylene. These solvents may be used alone or in combination of two or more. After being used in the production of bisphenol, aromatic hydrocarbons can be recovered and purified by distillation or the like for reuse. When aromatic hydrocarbons are reused in this way, those with a low boiling point are preferred.

[0034] The aliphatic alcohol is an alkyl alcohol in which an alkyl group and a hydroxyl group are bonded. The aliphatic alcohol may be a monohydric alcohol in which an alkyl group and one hydroxyl group are bonded, or a polyhydric alcohol in which an alkyl group and two or more hydroxyl groups are bonded. The alkyl group may be linear or branched, unsubstituted, or part of the carbon atoms of the alkyl group may be substituted with an oxygen atom.

[0035] The aliphatic alcohol is preferably an alcohol having an alkyl group and one hydroxyl group bonded thereto, and from the viewpoint of compatibility with the acid catalyst, is more preferably an alcohol having an alkyl group having 1 to 12 carbon atoms and one hydroxyl group bonded thereto, and is even more preferably an alcohol having an alkyl group having 1 to 8 carbon atoms and one hydroxyl group bonded thereto.

[0036] Specific examples of the aliphatic alcohol include 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, and triethylene glycol. One of the preferred aliphatic alcohols is methanol.

[0037] In addition, a large amount of the aromatic alcohol, which is the raw material, may be used in place of the organic solvent. In this case, the unreacted aromatic alcohol is lost, but the loss can be reduced by recovering and purifying it by distillation or the like and reusing it.

[0038] When a solvent is used, if the mass ratio of the solvent to the raw material ketone or aldehyde (solvent mass / ketone or aldehyde mass) is too high, the ketone or aldehyde and the aromatic alcohol do not react easily, and the reaction takes a long time. If the mass ratio is too low, the resulting bisphenol may cause poor mixing or may promote the polymerization of the ketone or aldehyde. For these reasons, the mass ratio of the solvent to the ketone or aldehyde is preferably 0.5 or more, more preferably 1 or more, and the upper limit may be adjusted within a range in which precipitation of the bisphenol occurs depending on the type of solvent, and may be 50 or less, or 30 or less.

[0039] The bisphenol produced is less likely to decompose if it is dispersed in the organic solvent rather than being completely dissolved therein. In addition, it is preferable to use a solvent in which bisphenol is less soluble, since this can reduce losses (e.g., losses to the filtrate during crystallization) when recovering bisphenol from the resulting bisphenol solution after the reaction is completed. Examples of solvents in which bisphenol is less soluble include aromatic hydrocarbons. For this reason, the organic solvent preferably contains an aromatic hydrocarbon, and one of the preferred aromatic hydrocarbons is toluene, since bisphenol is less soluble therein and has a low boiling point.

[0040] [Condensation reaction of ketones or aldehydes with aromatic alcohols] In the method for producing bisphenol according to the present embodiment, a ketone or aldehyde and an aromatic alcohol are condensed to produce a bisphenol represented by the following general formula (4) according to the following reaction formula (3). Bisphenols are produced.

[0041] [ka]

[0042] In general formula (3), R 1 ~R 6 has the same meaning as in general formulas (1) and (2).

[0043] [ka]

[0044] In general formula (4), R 1 ~R 6 has the same meaning as in general formulas (1) and (2).

[0045] Specific examples of the compound represented by the above general formula (4) include 2,2-bis(4-hydroxyphenyl)propane, 2,2-bis(4-hydroxy-3-methylphenyl)propane, 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane, 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, Examples of the hydroxyphenyl ether include, but are not limited to, 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, 2,2-bis(4-hydroxy-3-methylphenyl)heptane, 4,4-bis(4-hydroxyphenyl)heptane, and 4,4-bis(4-hydroxy-3-methylphenyl)heptane.

[0046] Among these, the method for producing 2,2-bis(4-hydroxy-3-methylphenyl)propane is preferred because it is easy to obtain bisphenol with a better color tone. In this specification, 2,2-bis(4-hydroxy-3-methylphenyl)propane is referred to as bisphenol C.

[0047] The method for preparing the reaction liquid is not particularly limited, and examples thereof include a method of mixing a solution containing an aromatic alcohol and a ketone or an aldehyde with a solution containing an acid catalyst, and a method of mixing a solution containing an aromatic alcohol and an acid catalyst with a solution containing a ketone or an aldehyde.

[0048] In order to suppress polymerization due to self-condensation of ketones or aldehydes, it is preferable to mix a solution containing an acid catalyst and an aromatic alcohol with a solution containing a ketone or an aldehyde. In this case, the solution containing an acid catalyst and an aromatic alcohol preferably contains a thiol co-catalyst.

[0049] Furthermore, the mixing of the solution containing the acid catalyst and the aromatic alcohol with the solution containing the ketone or aldehyde can usually be carried out by supplying the solution containing the ketone or aldehyde to the solution containing the acid catalyst and the aromatic alcohol. The solution containing the ketone or aldehyde may be supplied all at once or in portions. Since the reaction for producing bisphenol is an exothermic reaction, it is preferable to feed the solution containing the ketone or aldehyde in portions, for example by dropping it little by little.

[0050] The reaction for producing bisphenol is a condensation reaction between a ketone or aldehyde and an aromatic alcohol. When the reaction temperature of the condensation reaction is high, the polymerization of the ketone or aldehyde is likely to proceed. When the reaction temperature is low, the time required for the reaction is prolonged. For these reasons, the reaction temperature can be -30°C or higher, -20°C or higher, or -15°C or higher, and is preferably 0°C or higher, more preferably 5°C or higher, and even more preferably 10°C or higher, and is preferably 100°C or lower, more preferably 80°C or lower, and even more preferably 70°C or lower. The reaction temperature may be increased stepwise.

[0051] The reaction time of the condensation reaction is appropriately adjusted depending on the reaction conditions such as the production scale, the type of bisphenol produced, the reaction temperature, etc. If the reaction time is long, the produced bisphenol is easily decomposed, so the reaction time is preferably within 30 hours, more preferably within 25 hours, and even more preferably within 20 hours, and is usually 2 hours or more, and may be 5 hours or more, or 10 hours or more.

[0052] The reaction time includes the time required to mix the ketone or aldehyde with the aromatic alcohol (the time required to prepare the reaction solution). For example, when the ketone or aldehyde is supplied to a solution containing the aromatic alcohol and the acid catalyst over a period of 1 hour and then reacted for 2 hours, the reaction time is 3 hours. The supply time (dropping time) of the solution containing a ketone or aldehyde is appropriately adjusted depending on the cooling capacity of the reaction vessel, the production scale, the type of bisphenol to be produced, etc., and can be, for example, 0.3 hours or more or 0.5 hours or more, and can be, for example, 5 hours or less, 3 hours or less, or 1 hour or less, depending on the cooling capacity of the reaction vessel, etc. In this way, the bisphenol solution can be prepared while suppressing the generation of reaction heat.

[0053] The content of bisphenol in the bisphenol solution obtained by the reaction is not particularly limited, but is usually 10% by mass or more, preferably 15% by mass or more, more preferably 20% by mass or more, and even more preferably 25% by mass or more, and is usually 65% ​​by mass or less, preferably 60% by mass or less, more preferably 55% by mass or less, and even more preferably 50% by mass or less.

[0054] The pH of the bisphenol solution obtained by the reaction is not particularly limited, but since the reaction is carried out under an acid catalyst, it is usually 5.5 or less, but may be 5.0 or less, 4.5 or less, or 4.0 or less, and is usually 0 or more, 0.1 or more, 0.2 or more, or 0.3 or more. The temperature for measuring this pH is preferably room temperature (20 to 30°C), for example, 25°C.

[0055] <1-1-2. Neutralization> After the reaction step, the method further includes a neutralization step of neutralizing the organic layer of the reaction solution obtained in the reaction step. In the neutralization treatment, the acid catalyst in the bisphenol obtained by the condensation reaction can be neutralized and removed. Specifically, an organic phase containing bisphenol is mixed with desalted water or a basic aqueous solution, and then the mixture is separated into an organic phase and an aqueous phase. The aqueous phase is removed to obtain the organic phase. The organic phase is repeatedly washed with demineralized water and / or a basic aqueous solution until the pH of the aqueous phase to be removed is 7.5 or more and 13.0 or less, or 8.0 or more and 12.5 or less, or 8.5 or more and 12.0 or less. The basic aqueous solution may be an aqueous solution in which a basic substance such as sodium hydroxide or sodium bicarbonate is dissolved. When washing is performed multiple times, the same basic aqueous solution or different basic aqueous solutions may be used. The temperature for measuring the pH of the aqueous phase is preferably room temperature (20 to 30°C), for example, 25°C.

[0056] When the organic phase containing bisphenol is washed with water, the end point of the washing can be controlled by the electrical conductivity of the aqueous phase that is removed. If metal salts derived from the catalyst remain in the organic phase containing bisphenol, they cause a deterioration in color tone, so the electrical conductivity of the aqueous phase after washing is preferably 100 μS / cm or less, more preferably 50 μS / cm or less, and even more preferably 10 μS / cm or less. The temperature for measuring the electrical conductivity of the aqueous phase is preferably room temperature (20 to 30°C), for example, 25°C.

[0057] As the bisphenol solution to be used in each step after the reaction step, a mixed solution obtained by mixing bisphenol solutions obtained in different reaction steps may be used. The composition and characteristic conditions of the mixed solution when used as a mixed solution can be the composition and characteristic conditions of the bisphenol solution described above. In addition, when used as a mixed solution, it is preferable that at least one of the multiple reaction steps satisfies the above reaction step conditions, and it is more preferable that all reaction steps satisfies the above reaction step conditions.

[0058] <1-1-3. Purification process> The method for producing bisphenol according to this embodiment may further include, between the above-mentioned reaction step and the oxidation-reduction step described below, a step of purifying the bisphenol solution obtained by the reaction step, specifically, a step of purifying by means of crystallization, column chromatography, etc. Crystallization is preferred as a purification means from the viewpoints of ease of operation and economic efficiency, and in this case, the method for producing bisphenol according to this embodiment includes a purification step of crystallizing the bisphenol solution obtained by the reaction to obtain a bisphenol composition, and then dissolving the bisphenol composition in an organic solvent to obtain a bisphenol solution. When crystallization is carried out, the organic phase of the bisphenol solution may be cooled to effect crystallization. When a large amount of aromatic alcohol is used, the excess aromatic alcohol may be distilled off prior to the crystallization, and then the crystallization may be carried out. Crystallization may be performed multiple times. For example, when the method for producing bisphenol according to this embodiment has a second purification step, a second purification step may be further performed between the first purification step and the oxidation-reduction step described later, in which a bisphenol composition is obtained by crystallizing a bisphenol solution, and then the bisphenol composition is dissolved in an organic solvent to obtain a bisphenol solvent. The conditions of the second purification step can be similarly applied to the conditions of the purification step described above. In this way, by repeating the purification steps, a third purification step may be performed, or a fourth purification step may be performed. However, since a part of the bisphenol is dissolved in the mother liquor during crystallization and is lost, the number of times is preferably 5 or less, and more preferably 3 or less.

[0059] Specifically, the crystallization treatment can be carried out by cooling the bisphenol solution obtained by the reaction step or the organic phase containing bisphenol obtained by the neutralization treatment. The cooling temperature for crystallization is not particularly limited, but if the cooling temperature is too high, crystals will not precipitate sufficiently, so the cooling temperature is usually 30° C. or lower, preferably 25° C. or lower, more preferably 20° C. or lower, and even more preferably 15° C. or lower, and is usually −30° C. or higher, preferably −20° C. or higher, and more preferably −15° C. or higher. It is more preferable that the temperature is -10°C or higher. The cooling time for crystallization is not particularly limited, and it is preferable to continue the cooling until the desired amount is obtained.

[0060] The type of solvent for dissolving the bisphenol composition obtained by crystallization is not particularly limited, and examples thereof include aromatic hydrocarbons such as toluene, xylene, and benzene, ethers such as tetrahydrofuran and 4-methyltetrahydropyran, and alcohols such as methanol and ethanol, and from an economical viewpoint, toluene, xylene, or benzene is preferred. The organic solvent may be used alone or in any combination and ratio of two or more kinds.

[0061] The content of bisphenol in the bisphenol solution obtained by dissolving the crystallized bisphenol in an organic solvent is not particularly limited, but from an economical viewpoint, it is usually 10% by mass or more, preferably 15% by mass or more, more preferably 17% by mass or more, and even more preferably 20% by mass or more. Furthermore, if the bisphenol concentration during crystallization is too high, it will inhibit crystal growth and will cause problems such as pipe clogging during withdrawal due to deterioration of fluidity, so the content is usually 60% by mass or less, preferably 50% by mass or less, more preferably 45% by mass or less, and even more preferably 40% by mass or less. The content of the organic solvent in the bisphenol solution obtained by dissolving the crystallized bisphenol in an organic solvent is not particularly limited, but if the bisphenol concentration during crystallization is too high, it will inhibit crystal growth and will cause problems such as blockage of piping during withdrawal due to deterioration of fluidity, so the content is usually 1 mass% or more, preferably 5 mass% or more, more preferably 10 mass% or more, and even more preferably 15 mass% or more, and from an economical viewpoint, it is usually 95 mass% or less, preferably 85 mass% or less, more preferably 80 mass% or less, and even more preferably 75 mass% or less.

[0062] The pH of the bisphenol solution after the purification step is not particularly limited, but from the viewpoint of stabilizing the polymerization activity, it is usually 6.5 or more, preferably 6.6 or more, more preferably 6.7 or more, and even more preferably 6.8 or more, and is usually 8.0 or less, preferably 7.7 or less, more preferably 7.5 or less, and even more preferably 7.4 or less. The temperature for measuring this pH is preferably room temperature (20 to 30°C), for example, 25°C.

[0063] The purification step may be performed after the oxidation-reduction step described below, and the content of bisphenol in the oxidation-reduction treated solution obtained by the oxidation-reduction step can be increased.

[0064] The bisphenol solution to be subjected to each step after the purification step may be a mixed solution obtained by mixing the bisphenol solution obtained in the reaction step with a bisphenol solution obtained by subjecting the bisphenol solution obtained in the reaction step to a purification step, or a mixed solution obtained by mixing the bisphenol solution obtained in the reaction step with a bisphenol solution obtained by subjecting the bisphenol solution obtained in the reaction step to a purification step. The composition and property conditions of the mixed solution when the mixed solution is used may be the same as those of the bisphenol solution described above.

[0065] <1-2. Second bisphenol solution> The case where the bisphenol solution is a second bisphenol solution, that is, a bisphenol solution obtained by dissolving a bisphenol composition in an organic solvent, will be described below. The method for dissolving the bisphenol composition in an organic solvent to obtain a bisphenol solution is not particularly limited. For example, the method for dissolving the bisphenol composition in an organic solvent in the above purification step may be The method of dissolving to obtain a bisphenol solution can be similarly applied. The bisphenol composition is not particularly limited as long as it contains bisphenol, and may contain components other than bisphenol, for example, the bisphenol composition described in "1-2. Purification step" above may be used, and specifically, it may be a bisphenol composition prepared through the reaction step, neutralization step, and purification step described above. The form of the bisphenol composition is not particularly limited, but it is usually a solid. The type of bisphenol contained in the bisphenol composition is not particularly limited, and may be the bisphenol described in the first bisphenol solution described above. The content of bisphenol in the bisphenol composition is not particularly limited, but from the viewpoint that a small content is not economical and a large content does not form a homogeneous solution, the content is usually 0.1% by mass or more, preferably 0.5% by mass or more, more preferably 1% by mass or more, and even more preferably 5% by mass or more, and is usually 90% by mass or less, preferably 85% by mass or less, more preferably 80% by mass or less, and even more preferably 75% by mass or less. The bisphenol composition may contain components other than bisphenol, such as cresols, phenols, and xylenols. Furthermore, the type of organic solvent for dissolving the bisphenol composition is not particularly limited, and may be the organic solvent described above in relation to the first bisphenol solution. The second bisphenol solution may contain components other than the bisphenol composition and the organic solvent.

[0066] The content of bisphenol in the bisphenol solution is not particularly limited, but from an economical viewpoint, it is usually 10% by mass or more, preferably 15% by mass or more, more preferably 17% by mass or more, and even more preferably 20% by mass or more. Furthermore, if the bisphenol concentration during crystallization is too high, it will inhibit crystal growth and cause problems such as blockage of piping during withdrawal due to deterioration of fluidity, so the content is usually 60% by mass or less, preferably 50% by mass or less, more preferably 45% by mass or less, and even more preferably 40% by mass or less. The content of the organic solvent in the bisphenol solution is not particularly limited, but from the viewpoints that a small content is not economical and that a large content does not form a homogeneous solution, the content is usually 0.1 mass% or more, preferably 0.5 mass% or more, more preferably 1 mass% or more, and even more preferably 5 mass% or more, and is usually 90 mass% or less, preferably 85 mass% or less, more preferably 80 mass% or less, and even more preferably 75 mass% or less.

[0067] <1-3. Oxidation-reduction process> The method for producing bisphenol according to the present embodiment includes an oxidation-reduction step in which an oxidizing agent is added to a bisphenol solution, followed by addition of a reducing agent. As described above, the present inventors have found that the cause of color deterioration is a component (a component causing color deterioration) that is generated by oxidation with an oxidizing agent and then reduction with a reducing agent, and that is contained in the aqueous phase when the organic phase and the aqueous phase are separated. Therefore, by removing the component causing color deterioration from the oxidized and reduced solution as wastewater, the amount of the component causing color deterioration in the solution can be reduced, i.e., bisphenol with good color can be produced. The method for adding the oxidizing agent and the method for adding the reducing agent to the bisphenol solution are not particularly limited, and may be carried out by a known method, and may be carried out while appropriately stirring. The oxidation-reduction treatment may be carried out only once, or may be carried out multiple times. Further, a separate treatment may be carried out between the oxidation treatment and the reduction treatment, but it is preferable to carry out these treatments consecutively.

[0068] The type of oxidizing agent is not particularly limited, and examples thereof include hydrogen peroxide solution, chlorate solution, and hypochlorite solution. From the viewpoint that it is preferable that the oxidizing agent is colorless, hydrogen peroxide water, chloric acid water, or hypochlorite water is preferred, and hydrogen peroxide water is particularly preferred. The organic solvent may be used alone or in any combination and ratio of two or more kinds.

[0069] The type of reducing agent is not particularly limited, and for example, sodium citrate, sodium thiosulfate, sodium sulfite, oxalic acid, sodium borohydride, etc. can be used, and from the viewpoints of ease of handling, stability, and safe handling, sodium citrate, sodium thiosulfate, and sodium sulfite are preferred, and sodium citrate is particularly preferred. The organic solvent may be used alone or in any combination and ratio of two or more kinds.

[0070] In the bisphenol solution, the mass ratio of the oxidizing agent to the bisphenol is not particularly limited, but from the viewpoint that a small ratio will not be effective and a large ratio will increase the load on wastewater treatment, the mass ratio is usually 0.00001 or more, preferably 0.0005 or more, more preferably 0.001 or more, and even more preferably 0.005 or more, and is usually 10 or less, preferably 5 or less, more preferably 1 or less, and even more preferably 0.5 or less. In the bisphenol solution, the mass ratio of the reducing agent to the bisphenol is not particularly limited, but from the viewpoint that a small ratio will not be effective and a large ratio will increase the load on wastewater treatment, the mass ratio is usually 0.00001 or more, preferably 0.0005 or more, more preferably 0.001 or more, and even more preferably 0.005 or more, and is usually 10 or less, preferably 5 or less, more preferably 1 or less, and even more preferably 0.5 or less.

[0071] The content of bisphenol in the oxidation-reduction treated solution obtained by the oxidation-reduction step is not particularly limited, but from the viewpoints that if the content is too high, the bisphenol will precipitate and the effect will not be obtained, and if the content is too low, the efficiency will deteriorate, the content is usually 0.1 mass% or more, preferably 0.5 mass% or more, more preferably 1 mass% or more, and even more preferably 5 mass% or more, and is usually 80 mass% or less, preferably 70 mass% or less, more preferably 60 mass% or less, and even more preferably 50 mass% or less.

[0072] The pH of the oxidation-reduction treated solution obtained by the oxidation-reduction step is not particularly limited, but from the viewpoint of allowing the oxidizing agent and reducing agent to exist stably and act on the bisphenol, it is usually 1 or more, preferably 2 or more, more preferably 3 or more, and even more preferably 4 or more, and is usually 12 or less, preferably 11 or less, more preferably 10 or less, and even more preferably 9 or less. The temperature for measuring this pH is preferably room temperature (20 to 30°C), and for example, 25°C is preferable.

[0073] In the solution after the above-mentioned oxidizing agent and reducing agent addition treatment, the method for separating the components that cause the deterioration in color tone is not particularly limited, and the components may be separated by leaving the solution to stand, or the components used in general separation operations may be added to separate the components.

[0074] <1-4. Concentration process> The method for producing bisphenol according to this embodiment may include a concentration step of concentrating the oxidation-reduction treated solution obtained in the above-mentioned oxidation-reduction step, thereby recovering bisphenol in the solution. The method for concentrating the bisphenol is not particularly limited, and a known method can be applied. For example, when a crystallization process is applied, a solid bisphenol can be obtained, and the crystallization process described in the above-mentioned purification process can be performed. As a means other than the crystallization treatment, a solid-liquid separation method such as a centrifugal separation method can be used, and this method can provide solid bisphenol.

[0075] <2. Uses of bisphenol> The bisphenol obtained by the above-mentioned method for producing bisphenol can be used as a raw material for various thermoplastic resins such as polyether resins, polyester resins, polyarylate resins, polycarbonate resins, polyurethane resins, and acrylic resins, which are used for various applications such as optical materials, recording materials, insulating materials, transparent materials, electronic materials, adhesive materials, and heat-resistant materials, and various thermosetting resins such as epoxy resins, unsaturated polyester resins, phenolic resins, polybenzoxazine resins, and cyanate resins. It can also be used as a curing agent, additive, or precursor thereof. Furthermore, it is also useful as an additive such as a color developer, a discoloration inhibitor, a bactericide, or an antibacterial and antifungal agent for thermal recording materials, etc.

[0076] Among these, it is preferable to use it as a raw material (monomer) of thermoplastic resin or thermosetting resin because it can impart good mechanical properties, and more preferably as a raw material of polycarbonate resin or epoxy resin. It is also preferable to use it as a color developer, and more preferably to use it in combination with a leuco dye or a discoloration temperature regulator.

[0077] <3. Manufacturing method of polycarbonate resin> Another embodiment of the present invention is a method for producing a polycarbonate resin, comprising a step of polymerizing a polycarbonate resin using the bisphenol obtained by the above-mentioned production method as a raw material (hereinafter, also simply referred to as a "method for producing a polycarbonate resin").

[0078] A method for producing a polycarbonate resin, which comprises a step of polymerizing a polycarbonate resin using the bisphenol obtained by the above-mentioned production method as a raw material, will now be described. The polycarbonate resin is produced by, for example, transesterifying the above-mentioned bisphenol with a carbonate diester such as diphenyl carbonate in the presence of an alkali metal compound and / or an alkaline earth metal compound. The above-mentioned transesterification can be carried out by appropriately selecting a known method, but an example of a production method using bisphenol and diphenyl carbonate as raw materials will be described below.

[0079] In the above-mentioned method for producing polycarbonate resin, it is preferable to use an excess amount of diphenyl carbonate relative to the bisphenol in the bisphenol. The amount of diphenyl carbonate used relative to the bisphenol is preferably large in terms of the amount of terminal hydroxyl groups in the produced polycarbonate resin and excellent thermal stability of the polymer, and is preferably small in terms of the rate of transesterification reaction being fast and easy production of a polycarbonate resin with a desired molecular weight. For these reasons, the amount of diphenyl carbonate used relative to 1 mole of bisphenol is usually 1.001 moles or more, preferably 1.002 moles or more, and usually 1.3 moles or less, preferably 1.2 moles or less.

[0080] As for the method of supplying the raw materials, bisphenol and diphenyl carbonate can be supplied in a solid state, but it is preferable to melt one or both of them and supply them in a liquid state.

[0081] When producing a polycarbonate resin by the transesterification reaction of diphenyl carbonate and bisphenol, a transesterification catalyst is usually used. In the above-mentioned 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 any combination and ratio of two or more. In practical terms, it is preferable to use an alkali metal compound.

[0082] The amount of the transesterification catalyst used per mole of bisphenol or diphenyl carbonate is usually 0.05 μmol or more, preferably 0.08 μmol or more, more preferably 0.10 μmol or more, and usually 100 μmol or less, preferably 50 μmol or less, more preferably 20 μmol or less.

[0083] When the amount of the transesterification catalyst used is within the above range, it is easy to obtain the polymerization activity required for producing a polycarbonate resin having a desired molecular weight, and it is easy to obtain a polycarbonate resin that has excellent polymer hue, does not undergo excessive polymer branching, and has excellent fluidity during molding.

[0084] In producing a polycarbonate resin by the above method, it is preferred to continuously feed both of the above raw materials to a raw material mixing tank, and then continuously feed the resulting mixture and the transesterification catalyst to a polymerization tank. In the production of polycarbonate resins by the transesterification method, usually, both raw materials are fed into a raw material mixing tank, stirred uniformly, and then fed into a polymerization tank where a transesterification catalyst is added to produce a polymer.

[0085] In the production of polycarbonate resin, the polymerization time is appropriately adjusted depending on the production scale, the ratio of raw materials, the molecular weight of the desired polycarbonate resin, etc. If the polymerization time is long, deterioration in quality such as deterioration in color tone becomes apparent, so it is preferably 10 hours or less, more preferably 8 hours or less. The lower limit of the polymerization time can be 0.1 hours or more, or 0.3 hours or more.

[0086] In addition, when bisphenol is used as a raw material to produce a polycarbonate resin by melt polymerization, it tends to be difficult to obtain a polycarbonate resin having a high molecular weight. However, the bisphenol according to the present embodiment has excellent polymerization activity (high polymerization activity), so that a polycarbonate having a large molecular weight can be efficiently produced. In the method for producing a polycarbonate resin according to the present embodiment, by using the bisphenol according to the present embodiment, such a polycarbonate resin having a high molecular weight (for example, a viscosity average molecular weight of 10,000 to 100,000 or 24,000 to 50,000) can be produced in a short polymerization time (for example, 3 hours or less). In addition, in the method for producing a polycarbonate resin according to the present embodiment, by using the bisphenol according to the present embodiment, a polycarbonate resin having an excellent color tone can be obtained. EXAMPLES

[0087] The present invention will be described in more detail below with reference to examples and comparative examples. However, the present invention is not limited to the following examples as long as it does not depart from the gist of the present invention.

[0088] [Raw materials and reagents] In the following examples and comparative examples, orthocresol, toluene, sodium hydroxide, 98% sulfuric acid, dodecanethiol, acetone, acetaldehyde, sodium bicarbonate, cesium carbonate, acetonitrile, acetic acid, ammonium acetate, and reagents manufactured by Fujifilm Wako Pure Chemical Industries, Ltd. were used. Diphenyl carbonate used was a product manufactured by Mitsubishi Chemical Corporation.

[0089] [analysis] <Analysis of Bisphenol C> The compositional analysis of bisphenol was carried out by high performance liquid chromatography under the following conditions. The bisphenol obtained in each of the following examples was bisphenol C, and its purity is usually 99% by mass or more. Therefore, in this analysis, it was confirmed that the obtained solid was bisphenol C. This was used to confirm that C. Equipment: Shimadzu Corporation "LC-2010A" Imtakt ScherzoSM-C18 3μm 250mm×3.0mm ID·Low-pressure gradient method ·Analysis temperature: 40 °C ·Eluent composition: Solution A Ammonium acetate: Acetic acid: Deionized water = 3.000 g: 1 mL: 1 L solution Solution B Ammonium acetate: Acetic acid: Acetonitrile: Deionized water = 1.500 g: 1 mL: 900 mL: 150 mL solution ·At 0 minutes of analysis time, the eluent composition is Solution A: Solution B = 60:40 (volume ratio, the same below). From 0 to 41.67 minutes of analysis time, Solution A: Solution B gradually changes to 10:90, From 41.67 to 50 minutes of analysis time, Solution A: Solution B is maintained at 10:90, Analysis was performed at a flow rate of 0.34 mL / min.

[0090] <Measurement of pH> The pH was measured using a pH meter "pH METER ES-73" manufactured by Horiba, Ltd. for the aqueous phase at 25 °C taken out from the flask.

[0091] <Electrical conductivity> The electrical conductivity was measured using a conductivity meter "COND METER D-71" manufactured by Horiba, Ltd. for the aqueous phase at 25 °C taken out from the flask.

[0092] <Melting color of bisphenol> The melting color of bisphenol was measured by putting 20 g of bisphenol C into a test tube "P-24" (24 mm φ × 200 mm) manufactured by Nippon Denshikagaku Glass Co., Ltd., melting it at 190 °C for 30 minutes, and using "SE6000" manufactured by Nippon Denshoku Industries Co., Ltd. to measure the Hazen color number.

[0093] [Reference Example 1] (1-1) Production of bisphenol C In a separable flask equipped with a thermometer, a dropping funnel, a jacket, and an anchor-type stirring blade, 320 g of toluene, 230 g of ortho-cresol, and 15 g of methanol were placed under a nitrogen atmosphere, and 95 g of 98% by mass sulfuric acid was added with stirring while maintaining the internal temperature at 10° C. or lower, to prepare mixed solution A1. Next, 65 g of acetone, 5 g of dodecanethiol, and 50 g of toluene were added to an Erlenmeyer flask and stirred to obtain a mixed liquid B1, which was then placed in the dropping funnel. While maintaining the mixed liquid A1 at 10°C or below, the mixed liquid B1 in the dropping funnel was added dropwise to the mixed liquid A1 over a period of one hour with stirring, and stirred for an additional two hours while maintaining the temperature at 10°C, to obtain a bisphenol solution C1 of bisphenol C. 190 g of 25% sodium hydroxide solution was added to the bisphenol solution C1, and the mixture was stirred and heated to 75° C., and then allowed to stand to separate into oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase D1. 100 g of desalted water was added to the organic phase D1 obtained at 75° C., and the mixture was allowed to stand to separate into oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase E1. 100 g of 3 wt % sodium bicarbonate solution was added to the obtained organic phase E1, and the mixture was stirred to neutralize, and then allowed to stand to separate the oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase F1. 100g of demineralized water was added to the obtained organic phase F1, stirred for 1 hour, and allowed to stand to separate the oil and water. After the oil-water separation, the aqueous phase 1 was removed from the bottom of the separable flask to obtain an organic phase G1. The obtained aqueous phase 1 had a conductivity of 525 μS / cm, but the organic phase was repeatedly washed with 100g of demineralized water until the aqueous phase was 10 μS / cm or less, to obtain an organic phase H1. The organic phase H1 was gradually cooled from 75° C. to 5° C. to precipitate crystals containing bisphenol C. The resulting slurry containing the crystals containing bisphenol C was subjected to solid-liquid separation using a centrifuge to obtain 180 g of a cake containing bisphenol C. Using an evaporator equipped with an oil bath, the low boiling points were distilled off under reduced pressure at an oil bath temperature of 90° C. to obtain 152 g of a white solid. A portion of the obtained white solid was identified as bisphenol C using high performance liquid chromatography. (1-2) Color of Bisphenol C The melt color of the bisphenol C obtained in (1-1) above was measured, and it was found to be 15 on the Hazen color scale.

[0094] [Reference example 2] (2-1) Production of bisphenol C In a separable flask equipped with a thermometer, a dropping funnel, a jacket, and an anchor-type stirring blade, 320 g of toluene, 230 g of ortho-cresol, and 15 g of methanol were placed under a nitrogen atmosphere, and 95 g of 98% by mass sulfuric acid was added with stirring while maintaining the internal temperature at 10° C. or lower, to prepare mixed solution A1. Next, 65 g of acetone, 5 g of dodecanethiol, and 50 g of toluene were added to an Erlenmeyer flask and stirred to obtain a mixed liquid B1, which was then placed in the dropping funnel. While maintaining the mixed liquid A1 at 10° C. or less, the mixed liquid B1 in the dropping funnel was added dropwise to the mixed liquid A1 over a period of one hour with stirring, to obtain a bisphenol C solution C1′ of bisphenol C. Furthermore, 4 g of acetaldehyde was placed in the dropping funnel, and acetaldehyde was supplied to the bisphenol reaction solution C1' using the dropping funnel while maintaining the temperature at 10°C, and then the mixture was stirred for an additional 2 hours to obtain a bisphenol solution C2 of bisphenol C. 190 g of 25% sodium hydroxide solution was added to the bisphenol solution C2, stirred and heated to 75° C., and then allowed to stand to separate into oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase D1. 100 g of desalted water was added to the organic phase D1 obtained at 75° C., and the mixture was allowed to stand to separate into oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase E1. 100 g of 3 wt % sodium bicarbonate solution was added to the obtained organic phase E1, and the mixture was stirred to neutralize, and then allowed to stand to separate the oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase F1. 100g of demineralized water was added to the obtained organic phase F1, stirred for 1 hour, and allowed to stand to separate the oil and water. After the oil-water separation, the aqueous phase 1 was removed from the bottom of the separable flask to obtain an organic phase G1. The obtained aqueous phase 1 had a conductivity of 625 μS / cm, but the organic phase was repeatedly washed with 100g of demineralized water until the aqueous phase was 10 μS / cm or less, to obtain an organic phase H1. The organic phase H1 was gradually cooled from 75° C. to 5° C. to precipitate crystals containing bisphenol C. The resulting slurry containing the crystals containing bisphenol C was subjected to solid-liquid separation using a centrifuge to obtain 160 g of a cake containing bisphenol C. Using an evaporator equipped with an oil bath, the low boiling components were distilled off under reduced pressure at an oil bath temperature of 90° C. to obtain 140 g of a white solid. A portion of the obtained white solid was identified as bisphenol C using high performance liquid chromatography. (1-2) Color of Bisphenol C The melt color of the bisphenol C obtained in (1-1) was measured and found to be 87 on the Hazen color scale.

[0095] [Reference example 3] 67 g of bisphenol C having a Hazen color number (APHA) of 15 obtained in Reference Example 1 and 100 g of bisphenol C having a Hazen color number (APHA) of 87 obtained in Reference Example 2 were placed in a 500-liter plastic container and thoroughly mixed to obtain a bisphenol C mixture. The melt color of the obtained bisphenol C mixture was measured, and the Hazen color number (APHA) was 58.

[0096] [Example 1] In a separable flask equipped with a thermometer, a dropping funnel, a jacket, and an anchor-type stirring blade, 50 g of the bisphenol C mixture obtained in Reference Example 3, 100 g of toluene, and 100 g of 5% by mass hydrogen peroxide solution were placed under a nitrogen atmosphere, and the temperature was then raised to 75° C. Then, the mixture was allowed to stand to separate into oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask, and an organic phase 1 was obtained. 100 g of a 5% by mass aqueous solution of sodium citrate was added to the obtained organic phase 1 and stirred for 1 hour. Then, the mixture was left to stand to separate into oil and water. After the oil-water separation, the aqueous phase was removed from the bottom of the separable flask to obtain an organic phase 2. 100 g of demineralized water was added to the obtained organic phase 2 and stirred for 1 hour. Then, the mixture was left to stand to separate the oil and water. After the oil and water separation, the aqueous phase 1 was removed from the bottom of the separable flask to obtain an organic phase 3. The electrical conductivity of the obtained aqueous phase 1 was 734 μS / cm, but the organic phase was repeatedly washed with 100 g of demineralized water until the electrical conductivity of the aqueous phase was 10 μS / cm or less, to obtain an organic phase 4. The organic phase 4 was gradually cooled from 75° C. to 5° C. to precipitate crystals containing bisphenol C. The resulting slurry containing the crystals containing bisphenol C was subjected to solid-liquid separation using a centrifuge to obtain 40 g of a cake containing bisphenol C. Using an evaporator equipped with an oil bath, low boiling fractions were distilled off under reduced pressure at an oil bath temperature of 90°C to obtain 25 g of a white solid. A part of the obtained white solid was confirmed to be bisphenol C using high performance liquid chromatography. The color tone of the obtained bisphenol C was measured, and the Hazen color number (APHA) was 30.

[0097] [Comparative Example 1] Bisphenol C was obtained in the same manner as in Example 1, except that neither the 100 g of 5 mass % hydrogen peroxide solution nor the 100 g of 5 mass % aqueous sodium citrate solution was added. The color tone of the obtained bisphenol C was measured, and the Hazen color number (APHA) was 38.

[0098] [Comparative Example 2] Bisphenol C was obtained in the same manner as in Example 1, except that 100 g of 5 mass % hydrogen peroxide water was not added. When the color tone of the obtained bisphenol C was measured, the Hazen color scale (APHA) was 38.

[0099] [Comparative Example 3] Bisphenol C was obtained in the same manner as in Example 1, except that 100 g of the 5% by mass aqueous sodium citrate solution was not added. The obtained bisphenol C had a worse color tone than the bisphenol C mixture, and was severely colored.

[0100] The Hazen color number (APHA) of the bisphenol C mixture in Example 1 and Comparative Examples 1 to 3, the use or non-use of an oxidizing agent, the use or non-use of a reducing agent, and the color number (APHA) of the resulting bisphenol C are summarized in Table 1 below. From Table 1 below, it can be seen that for a bisphenol C mixture, the color tone of the bisphenol C is greatly improved by adding an oxidizing agent and then a reducing agent.

[0101] [Table 1]

Claims

1. A method for producing bisphenol, comprising the steps of: The method includes an oxidation-reduction step of adding an oxidizing agent to a bisphenol solution and then adding a reducing agent, The bisphenol solution is A method for producing bisphenol, comprising a reaction step in which a ketone or aldehyde is subjected to a condensation reaction with an aromatic alcohol in the presence of an acid catalyst and a thiol co-catalyst to produce a bisphenol, followed by a neutralization step in which an organic layer of the reaction solution obtained in the reaction step is neutralized.

2. The bisphenol solution is 2. The method for producing bisphenol according to claim 1, wherein the solution is obtained by a purification step of purifying the solution obtained in the neutralization step to obtain a bisphenol composition, and a step of dissolving the bisphenol composition obtained in the purification step in an organic solvent.

3. The method for producing bisphenol according to claim 1 or 2, wherein the ketone or aldehyde is acetone or acetaldehyde.

4. The method for producing bisphenol according to claim 1 or 2, wherein the ketone or aldehyde is a ketone.

5. The method for producing bisphenol according to any one of claims 1 to 4, wherein the bisphenol is 2,2-bis(4-hydroxy-3-methylphenyl)propane.

6. A method for producing a polycarbonate resin, comprising a step of polymerizing a polycarbonate resin using, as a raw material, a bisphenol produced by the method for producing bisphenol according to any one of claims 1 to 5.

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