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
  • C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
  • C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
  • C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
  • C08G8/10—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenol
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
  • C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
  • C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols

Definitions

• the present invention relates to a water-soluble resole-type phenol resin having a reduced content of formaldehyde and phenol.
• Phenol resin is a typical thermosetting resin used in many fields due to its heat resistance and high mechanical strength. Phenol resins are used, for example, by impregnating or applying them to various base materials, or as binders for various organic and inorganic base materials. Phenol resins are roughly classified into novolak-type phenol resins that are heat-cured by adding a curing agent such as hexamethylenetetramine and resol-type phenol resins that are heat-cured by themselves. It has been.
• phenolic resins hydrophilicity is used in applications where ammonia-free is required for environmental friendliness and work environment improvement, and when solvent-free is required, applications used in the form of aqueous solutions or emulsions.
• High resole-type phenolic resins are often used.
• the water-soluble resole resin is used, for example, as a binder for abrasive cloth.
• Resol resin has excellent abrasive grain holding power and heat resistance, and high grindability can be obtained.
• this resol-type phenolic resin contains unreacted phenols and aldehydes, which are undesired substances from the viewpoint of protecting the air environment and the human environment.
• an excess amount of phenol may be reacted with aldehydes, but a resol-type phenol resin obtained by using an excess amount of phenol. Since it contains a large amount of unreacted phenols, it has poor curability, and the obtained cured product does not satisfy the mechanical strength required by the market.
• the resol-type phenol resin obtained by using an excess amount of phenol with respect to aldehydes contains a large amount of unreacted phenol, and therefore, it is not preferable to use it from the viewpoint of environment and occupational safety and health.
• Patent Document 1 describes a method for producing a resol resin capable of reducing the amount of unreacted monomers such as formaldehyde and phenol.
• the number of moles of the phenol component in the novolak resin and the alkali metal hydroxide as a catalyst are used in a specific ratio, and the aldehydes and the phenols are reacted in a specific ratio. It is described to control the content of unreacted phenols.
• Patent Document 1 can reduce the content of unreacted phenols to a very low level, unreacted formaldehyde remained in an unavoidable amount.
• An object of the present invention is to provide a resol-type phenol resin having water solubility while the residual amount of both phenol and aldehyde, which are unreacted monomers, is significantly reduced.
• a water-soluble resole-type phenol resin having an unreacted phenol content of 0.1% by mass or less and an unreacted aldehyde content of 0.1% by mass or less.
• the residual amount of unreacted phenol and unreacted aldehyde is both reduced, and the resin is water-soluble, thereby reducing the environmental load and the load on the human body, and has a wider range of application. Is provided.
• the resol-type phenol resin of the present embodiment is a water-soluble phenol resin, and the content of unreacted phenol is 0.1% by mass or less, and the content of unreacted aldehyde is 0.1% by mass or less.
• the resol-type phenol resin of the present embodiment is produced by reacting the novolak-type phenol resin (A) with aldehydes in the presence of a catalyst using specific reaction conditions.
• the novolak-type phenol resin (A) used for producing the resol-type phenol resin of the present embodiment is obtained by reacting phenols with aldehydes. At that time, by controlling the content and molecular weight of the unreacted phenols remaining in the novolak-type phenol resin resin, the unreacted phenols and unreacted aldehydes remaining in the finally obtained resol-type phenol resin can be obtained. It can be reduced.
• the novolak type phenol resin (A) can be produced, for example, through the following steps. First, phenols and aldehydes are reacted at 100 ° C. for 1 to 5 hours in the presence of an acid catalyst. Then, the unreacted phenol contained in the obtained reaction mixture is azeotropically removed at a temperature of 150 ° C. to 180 ° C. under reduced pressure while adding water.
• the content of unreacted phenol remaining in the novolak type phenol resin is preferably 0.1% by mass or less, more preferably 0.09% by mass or less, still more preferably 0.08% by mass or less, and particularly preferably. Is particularly preferably reduced to an amount of about 0.01% by mass.
• the molar ratio is less than 0.3, the yield deteriorates as the molar ratio decreases, which is economically unfavorable.
• it exceeds 0.6 it becomes difficult to adjust the molecular weight of the novolak-type phenol resin as a product, which is not preferable.
• the phenols used as a raw material for producing the novolak-type phenol resin (A) are not particularly limited, and are, for example, phenols; alkylphenols such as cresol, xylenol, ethylphenol, butylphenol, and octylphenol; resorcin, Polyphenols such as catechol; halogenated phenols such as fluorophenols, chlorophenols, bromophenols, iodophenols; monovalent phenol substitutions such as phenylphenols, aminophenols, nitrophenols, dinitrophenols, trinitrophenols; and naphthols. And so on.
• these phenols are not limited to only one type in their use, and two or more types can be used in combination. Resorcin and phenol are preferable in order to obtain a water-soluble resor-type phenol resin which is the final target product, and phenol is preferable from the viewpoint of obtaining an inexpensive product.
• aldehydes used as raw materials for producing the novolak type phenol resin (A) formaldehyde, paraformaldehyde, formaldehyde such as trioxane, acetaldehyde, etc., which are commonly used in the production of phenol resin, are effective. Urotropin can also be used. Of these, formaldehyde is preferable. As the aldehydes, one kind may be used alone, or two or more kinds may be used in combination.
• an acid generally used in the production of the novolak resin can be used, for example, oxalic acid, hydrochloric acid, phosphoric acid, sulfuric acid, paratoluene sulfone.
• examples thereof include acid, phenol sulfonic acid, zinc acetate and zinc octylate which are catalysts for high ortho-novolac resin.
• the novolak type phenol resin (A) As the novolak type phenol resin (A), a so-called modified novolak resin obtained by reacting phenol with, for example, an epoxy resin, triazines, etc. at an arbitrary ratio in the process of synthesizing the novolak resin can also be used.
• the novolak resin modified by these is used as a raw material in the production of the resol resin, it is possible to impart water resistance and heat resistance to the resol resin produced by the method of the present invention.
• the resole-type phenol resin of the present embodiment can be produced by using the above-mentioned novolak-type phenol resin (A) by the following method.
• the resol-type phenol resin of the present embodiment can be produced by reacting the above-mentioned novolak-type phenol resin (A) with aldehydes in the presence of a basic catalyst.
• a basic catalyst alkali metal hydroxides such as lithium hydroxide, sodium hydroxide and cariu hydroxide; hydroxides of alkaline earth metals such as magnesium hydroxide, calcium hydroxide and barium hydroxide; ammonia, Primary amines such as monoethanolamine, secondary amines such as diethanolamine; and tertiary or zinc acetate such as trimethylamine, triethylamine, triethanolamine, diazabicycloundecene and the like can be used.
• an alkali metal hydroxide it is preferable to use an alkali metal hydroxide, and it is particularly preferable to use sodium hydroxide.
• These catalysts may be reacted by one kind or a combination of two kinds. Further, sulfuric acid, hydrochloric acid, phosphoric acid, p-toluenesulfonic acid and the like may be used for the purpose of neutralizing the catalyst.
• the molar ratio of [aldehyde] / [novolak-type phenol resin], which is the ratio of the novolak-type phenol resin (A) and aldehydes in the production of the resol-type phenol resin of the present embodiment, is that the unreacted novolak-type phenol resin component is used. 4. From the viewpoint that the physical properties such as curability of the obtained resol-type phenol resin are good without remaining, 0.5 or more is preferable, and from the viewpoint that unreacted formaldehyde does not remain and is preferable in terms of environmental measures. It is preferably 0 or less.
• the molar ratio of [aldehyde] / [novolak-type phenol resin] is further 1.0 to 2.5 (molar ratio). It is preferable, and 1.5 to 2.0 (molar ratio) is particularly preferable.
• the molar ratio of [aldehyde] / [novolak-type phenol resin] is information on the number average molecular weight Mn obtained by GPC measurement of the novolak-type phenol resin (A) obtained by the above method and the molecular weight of the aldehyde used. Based on the above, the weight of the novolak-type phenol form (A) to be used and the weight of the aldehyde can be adjusted by weighing them so as to have the desired number of moles.
• the basic catalyst is an alkali metal hydroxide
• the alkali metal hydroxide is [the number of moles of the novolak-type phenol resin] with respect to the novolak-type phenol resin (A) used as a raw material. It is preferable that the alkali metal is used in an amount such that the value of] is 5 to 15, preferably 8 to 12.
• the alkali metal hydroxide catalyst in the above amount, the residual amount of unreacted aldehydes can be reduced.
• the number of moles of the novolak-type phenol resin can be calculated from the number average molecular weight Mn obtained by GPS measurement of the novolak-type phenol resin (A) and the weight of the novolak-type phenol resin used.
• the number of moles of the alkali metal can be obtained from the molecular weight of the hydroxide of the alkali metal used. Therefore, the value of [number of moles of novolak-type phenol resin] / [number of moles of alkali metal] should be adjusted between the amount of novolak-type phenol resin (A) to be used and the amount of alkali metal hydroxide as a catalyst. Therefore, it can be controlled within a target range.
• the aldehyde used in the production of the resole-type phenol resin of the present embodiment and the alkali metal hydroxide as the basic catalyst are used in an amount such that the above-mentioned molar ratio is obtained based on the number average molecular weight of the novolak-type phenol resin. Will be done. Thereby, the amount of aldehyde remaining as an unreacted substance in the obtained resol type phenol resin can be highly controlled.
• oxalic acid was added as a reaction catalyst to a mixture of phenol and a 37% concentration formaldehyde aqueous solution, the temperature in the reaction system was set to 100 ° C., the reaction was carried out for 1 to 5 hours, and then methanol was added at 150 ° C. While performing vacuum distillation, a novolak type phenol resin (A) is obtained.
• the amount of residual phenol in the obtained novolak-type phenol resin resin (A) is 0.1% by mass or less, more preferably 0.09% by mass or less, still more preferably 0.08% by mass or less.
• the amount of residual phenol in the resol-type phenol resin thus obtained is 0.1% by mass or less, preferably 0.09% by mass or less, and more preferably 0.08 with respect to the resin. It is less than mass%.
• the amount of residual phenol in this resol-type phenol resin is 0.1% by mass or less, preferably 0.09% by mass or less, and more preferably 0.08% by mass or less with respect to the resin. be.
• the resole-type phenol resin of the present embodiment is provided in the form of an aqueous solution produced by the above method.
• the form of the aqueous solution means that the obtained resol-type phenol resin aqueous solution does not substantially contain an organic solvent such as methanol used in the manufacturing process thereof.
• the fact that the organic solvent is substantially not contained means that the organic solvent is contained in an amount of 0.1% by mass or less in the aqueous solution of the resole-type phenol resin.
• Example 1 A stirrer and a thermometer were set in a 2-liter four-necked flask, 400 g of phenol and 0.4 g of oxalic acid dihydrate were added, the temperature was raised to the reflux temperature (100 ° C.), and 138 g of 37% formalin was added. Dropped over time. After reacting at the reflux temperature for 1 hour, the mixture was distilled at normal pressure and the temperature was raised to 100 ° C. Then, the temperature was raised to 150 ° C. under a reduced pressure of 70 Torr, and 40 g of water was added dropwise under a reduced pressure over 1 hour to azeotropically remove phenol.
• the number average molecular weight of the produced novolak-type phenol resin was 500. Moreover, when the obtained reaction mixture was measured by gas chromatography, the amount of unreacted phenol was 0.1% by mass.
• the non-volatile content at 135 ° C. is 68%, the miscibility with water is 210%, the amount of unreacted phenol measured by gas chromatography is below the detection limit (0.1% by mass), and the amount of unreacted formaldehyde is. It was 0.07% by mass.
• Example 1 Since the resole-type phenol resin obtained in Example 1 has a residual amount of unreacted phenol and a residual amount of unreacted formaldehyde of 0.1% by mass or less, the Industrial Safety and Health Act Specified Chemical Substance Disorder Prevention Regulations (Hereinafter, "Safety Law Specialization Regulations") is excluded.
• Novolak resin (Ia) was obtained.
• the novolak-type phenol resin was diluted with methanol so as to have a solid content of 80%, and a methanol solution of the novolak resin (Ia) was tested below.
• the miscibility of this resin with water is 320%, and GPC.
• the unreacted phenol was below the detection limit as measured by.
• the amount of unreacted phenol measured by gas chromatography was 0.02% by mass.
• the amount of unreacted formaldehyde measured by gas chromatography was 0.6% by mass.
• the binding molar ratio of this resin measured by 13 C-NMR was 1.49.
• the softening point of the ring ball method (B & R method) was 45 ° C.
• a novolak resin (Ib) having a number average molecular weight of 610 and a binding molar ratio of 0.75 determined by 13 C-NMR was obtained.

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• Phenolic Resins Or Amino Resins (AREA)

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• 2021
  • 2021-08-25 JP JP2021574859A patent/JP7095820B1/ja active Active
  • 2021-08-25 EP EP21864201.5A patent/EP4212563A4/en active Pending
  • 2021-08-25 KR KR1020237011445A patent/KR20230062607A/ko active Pending
  • 2021-08-25 US US18/024,562 patent/US20230331895A1/en active Pending
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