Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
  • C08F216/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
  • C08F216/04—Acyclic compounds
  • C08F216/06—Polyvinyl alcohol ; Vinyl alcohol
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
  • C04B24/24—Macromolecular compounds
  • C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/12—Hydrolysis
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/48—Isomerisation; Cyclisation
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D129/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
  • C09D129/02—Homopolymers or copolymers of unsaturated alcohols
  • C09D129/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes

Definitions

• the present invention relates to a vinyl alcohol polymer, and an aqueous solution containing the vinyl alcohol polymer, a paint, and a cement admixture.
• Vinyl alcohol polymers have excellent film properties (mechanical strength, oil resistance, film-forming properties, oxygen gas barrier properties, etc.) due to their hydrophilicity or high crystallinity. For this reason, vinyl alcohol polymers are widely used as a raw material for viscosity adjusters (thickeners), adhesives, paper coating agents, fiber processing agents, binders, emulsion stabilizers, films, fibers, etc., taking advantage of these properties. Furthermore, in order to improve the performance of vinyl alcohol polymers to suit the application, modified vinyl alcohol polymers are being developed by introducing functional groups, controlling crystallinity, etc.
• the modified vinyl alcohol polymers described in Patent Documents 1 and 2 exhibit excellent thickening properties at low concentrations.
• an object e.g., an emulsion
• the above-mentioned modified vinyl alcohol polymer has problems in terms of handling, such as high viscosity at high concentrations making it impossible to pump the polymer or inability to dissolve the polymer at all.
• the present invention aims to solve the above problems, and aims to provide a vinyl alcohol-based polymer that can easily produce an aqueous solution of a vinyl alcohol-based polymer whose viscosity can be easily and greatly changed, an aqueous solution of a vinyl alcohol-based polymer whose viscosity can be easily and greatly changed, and a paint and a cement admixture that contain the vinyl alcohol-based polymer.
• the present invention includes the following inventions.
• a vinyl alcohol polymer the content of the vinyl alcohol polymer is 1.5% by mass, and the pH at 20° C. is 4, the aqueous solution viscosity X [cp] of the aqueous solution at a shear rate of 1 [1/s] at 20° C.;
• the vinyl alcohol-based polymer has a content of 1.5% by mass and a pH of 10 at 20° C. in an aqueous solution state, and the aqueous solution viscosity Y [cp] of the aqueous solution at a shear rate of 1 [1/s] at 20° C.
• a structural unit (A) having a lactone ring, a structural unit (B) having an ionic group, and a structural unit (C) having a hydrophobic group composed of a hydrocarbon having 3 or more carbon atoms The vinyl alcohol-based polymer according to any one of the above [1] to [3], which satisfies the following formula (3), where the content of the structural unit (A) is (a), the content of the structural unit (B) is (b), the content of the structural unit (C) is (c), the number of carbon atoms of the hydrophobic group in the structural unit (C) is (d), and the number of ionic groups in the structural unit (B) is (e), relative to all structural units of the vinyl alcohol-based polymer: 5 ⁇ (c ⁇ (d-3) 2 )/(a+b ⁇ e) ⁇ 95 (3)
• a vinyl alcohol polymer-containing aqueous solution comprising the vinyl alcohol polymer according to any one of [1] to [7] above and water.
• the present invention can provide a vinyl alcohol-based polymer that can easily produce an aqueous solution of a vinyl alcohol-based polymer whose viscosity can be easily and greatly changed, an aqueous solution of a vinyl alcohol-based polymer whose viscosity can be easily and greatly changed, and a paint and a cement admixture that contain the vinyl alcohol-based polymer.
• aqueous solution state refers to a state in which components other than the solvent (water) are dissolved or dispersed in water.
• the vinyl alcohol polymer according to the present invention is a vinyl alcohol polymer, the content of the vinyl alcohol polymer is 1.5% by mass, and the pH at 20° C. is 4, the aqueous solution viscosity X [cp] of the aqueous solution at a shear rate of 1 [1/s] at 20° C.;
• the vinyl alcohol-based polymer has a content of 1.5% by mass and a pH of 10 at 20° C. in an aqueous solution state, and the aqueous solution viscosity Y [cp] of the aqueous solution at a shear rate of 1 [1/s] at 20° C. satisfies the following formula (1): 1.5 ⁇ Y/X ⁇ 1,500 (1)
• the vinyl alcohol polymer according to the present invention has a large viscosity ratio (Y/X) of more than 1.5. Therefore, with the vinyl alcohol polymer according to the present invention, it is possible to easily change the viscosity significantly by changing the pH of an aqueous solution of the vinyl alcohol polymer. Therefore, when an aqueous solution of the vinyl alcohol polymer is transported through piping or the like, it is possible to easily make the aqueous solution low-viscosity by lowering the pH by adding an acid or the like, thereby enabling smooth transport. Furthermore, when used as a thickener or the like, it is possible to easily make the aqueous solution high-viscosity by increasing the pH by adding an alkali or the like.
• the viscosity ratio (Y/X) is more than 1.5 and less than 1,500. If it is 1.5 or less, the viscosity of the aqueous solution of the vinyl alcohol polymer cannot be easily changed, so that the pH If the pH is 1,500 or more, the viscosity changes significantly with a slight change in pH, making it difficult to adjust the viscosity and reducing convenience.
• the viscosity ratio (Y/X) is preferably more than 1.5 and not more than 1,000, more preferably more than 1.5 and not more than 800, even more preferably more than 1.5 and not more than 500, and still more preferably 3. 0 or more and 500 or less, more preferably 5.0 or more and 500 or less, more preferably 5.0 or more and 300 or less, more preferably 10 or more and 300 or less, more preferably 15 or more and 300 or less, more preferably Between 25 and 300.
• the viscosity ratio (Y/X) tends to increase when a structural unit having a hydrophobic group with a large number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is increased, when the degree of polymerization is increased, when the content of structural units having an ionic group is increased, or when the vinyl ester monomer units are decreased.
• the viscosity ratio (Y/X) tends to decrease when a structural unit having a hydrophobic group with a small number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is decreased, when the degree of polymerization is decreased, when the content of structural units having an ionic group is decreased, or when the vinyl ester monomer units are increased.
• the viscosity X [cp] is preferably 6,000 cp or less from the viewpoint of improving the liquid delivery property of the aqueous solution of the vinyl alcohol polymer.
• the viscosity X [cp] is preferably 1 cp or more from the viewpoint of thickening after changing the viscosity of the aqueous solution of the vinyl alcohol polymer. From this viewpoint, the viscosity X [cp] is preferably 1 to 6,000, more preferably 10 to 5,500, even more preferably 20 to 5,500, even more preferably 25 to 5,500, even more preferably 100 to 5,500, even more preferably 100 to 3,000, even more preferably 100 to 2,500, and even more preferably 130 to 2,500.
• the viscosity Y [cp] is preferably 20 cp or more from the viewpoint of viscosity changeability and thickening of the aqueous solution of the vinyl alcohol polymer. Also, the viscosity Y [cp] is preferably 500,000 cp or less from the viewpoint of handleability. From this viewpoint, the viscosity X [cp] is preferably 20 to 500,000, more preferably 100 to 300,000, even more preferably 100 to 200,000, even more preferably 200 to 200,000, even more preferably 500 to 200,000, even more preferably 2,000 to 200,000, even more preferably 5,000 to 200,000, even more preferably 6,000 to 200,000, even more preferably 10,000 to 150,000.
• the viscosity Y [cp] tends to increase when a structural unit having a hydrophobic group with a large number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is increased, when the degree of polymerization is increased, when the content of structural units having an ionic group is increased, or when the vinyl ester monomer units are decreased.
• the viscosity Y [cp] tends to decrease when a structural unit having a hydrophobic group with a small number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is decreased, when the degree of polymerization is decreased, when the content of structural units having an ionic group is decreased, or when the vinyl ester monomer units are increased.
• ⁇ Viscosity ratio (Y/Z)> The aqueous solution viscosity Y [cp] and the content of the vinyl alcohol polymer in the aqueous solution is 1.5% by mass and has a pH of 10 at 20° C.
• the aqueous solution has a shear rate of 100 [1/ It is preferable that the aqueous solution viscosity Z [cp] at the aqueous solution temperature [s] satisfies the following formula (2). 1.5 ⁇ Y/Z ⁇ 100 (2) When the viscosity ratio (Y/Z) is more than 1.5, the composition has excellent thixotropy, and when the viscosity ratio (Y/Z) is less than 100, the composition has excellent handleability.
• the viscosity ratio (Y/Z) is more preferably 2.0 to 80, even more preferably 5 to 80, still more preferably 10 to 80, still more preferably 20 to 80, and still more preferably It is preferably 20 to 60, and more preferably 20 to 50.
• the viscosity ratio (Y/Z) tends to increase when a structural unit having a hydrophobic group with a large number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is increased, when the content of structural units having an ionic group is increased, or when the vinyl ester monomer units are decreased. Also, the viscosity ratio (Y/Z) tends to decrease when a structural unit having a hydrophobic group with a small number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is decreased, when the content of structural units having an ionic group is decreased, or when the vinyl ester monomer units are increased.
• the viscosity Z [cp] is preferably 10,000 cp or less from the viewpoint of improving the liquid transportability of the aqueous solution of the vinyl alcohol polymer. Moreover, the viscosity Z [cp] is preferably 10 cp or more from the viewpoint of thickening. From this viewpoint, the viscosity Z [cp] is preferably 10 to 10,000, more preferably 50 to 10,000, even more preferably 100 to 10,000, still more preferably 100 to 6,000, still more preferably 100 to 4,000, still more preferably 500 to 4,000, and still more preferably 1,000 to 3,000.
• the viscosity Z [cp] tends to increase when a structural unit having a hydrophobic group with a large number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is increased, or when the content of structural units having an ionic group is increased; and the viscosity Z [cp] tends to decrease when a structural unit having a hydrophobic group with a small number of carbon atoms is introduced, when the content of structural units having a hydrophobic group is decreased, or when the content of structural units having an ionic group is decreased.
• aqueous solution viscosities X [cp], Y [cp], Z [cp], and W [cp] can be measured using a rheometer, and more specifically, can be measured by the method described in the Examples.
• ⁇ pH Adjuster> There is no particular limitation on the method for adjusting the pH of the aqueous solution of the vinyl alcohol polymer, but it is preferable to add an acidic compound or a basic compound to the aqueous solution.
• Acidic compounds include inorganic acids such as hydrochloric acid, sulfuric acid, phosphoric acid, nitric acid, and hydrofluoric acid; and organic acids such as formic acid, acetic acid, trichloroacetic acid, propionic acid, butanoic acid, chloroacetic acid, methanesulfonic acid, p-toluenesulfonic acid, trifluoromethanesulfonic acid, and citric acid.
• organic acids such as formic acid, acetic acid, trichloroacetic acid, propionic acid, butanoic acid, chloroacetic acid, methanesulfonic acid, p-toluenesulfonic acid, trifluoromethanesulfonic acid, and citric acid.
• p-toluenesulfonic acid, citric acid, hydrochloric acid, nitric acid, sulfuric acid, and acetic acid are preferred, and citric acid is more preferred.
• Examples of basic compounds include alkali metal hydrides such as sodium hydride and potassium hydride; alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; alkali metal carbonates such as sodium carbonate and potassium carbonate; alkali metal bicarbonates such as sodium hydrogen carbonate and potassium hydrogen carbonate; tertiary amines such as triethylamine, tributylamine, and diazabicyclo[2.2.2]octane; and nitrogen-containing heterocyclic aromatic compounds such as pyridine and 2,6-lutidine.
• alkali metal hydroxides are preferred, and sodium hydroxide is more preferred.
• the basic compounds may be used alone or in combination of two or more.
• the vinyl alcohol polymer according to the present invention preferably contains a structural unit (A) having a lactone ring.
• the lactone ring can be obtained, for example, by copolymerizing a vinyl ester and a (meth)acrylic acid ester, followed by saponification.
• the structural unit (A) having a lactone ring is preferably at least one selected from the group consisting of units represented by the following structural formula (1), units represented by the following structural formula (2), and units represented by the following structural formula (3), more preferably at least one selected from the group consisting of units represented by the following structural formula (1) and units represented by the following structural formula (2), and even more preferably a unit represented by the following structural formula (1).
• * denotes a bond bonding to an adjacent structural unit.
• R is a methyl group, a carboxy group, or a salt of a carboxy group.
• the vinyl alcohol polymer according to the present invention preferably contains a structural unit (B) having an ionic group.
• the vinyl alcohol-based polymer according to the present invention contains a structural unit (B) having an ionic group, and therefore has improved solubility in water when made into an aqueous solution.
• the structural unit (B) reacts with a hydroxyl group in the vinyl alcohol-based polymer to form a lactone ring structure, or the ionic group is protonated, thereby reducing the viscosity, and thus the aqueous solution can be smoothly transferred.
• the ionic group is not particularly limited, and examples thereof include carboxy groups, salts of carboxy groups, sulfo groups, salts of sulfo groups, amino groups, salts of amino groups, and salts of quaternary ammonium groups.
• carboxy groups salts of carboxy groups, sulfo groups, salts of sulfo groups, amino groups, salts of amino groups, and salts of quaternary ammonium groups.
• alkali metal salts are preferred, and sodium salts are more preferred.
• These ionic groups may be used alone or in combination of two or more types. Among these, from the viewpoints of viscosity modification and acidity, carboxy groups and salts of carboxy groups are preferred.
• the monomer constituting the structural unit (B) having an ionic group includes a monomer having a carboxy group or its salt, an ester of a monomer having a carboxy group, a monomer having a sulfo group or its salt, a monomer having an amino group or its salt, a monomer having a salt of a quaternary ammonium group, etc. These monomers may be used alone or in combination of two or more. Among these, from the viewpoint of viscosity modification and acidity, a monomer having a carboxy group or its salt, and an ester of a monomer having a carboxy group are preferred.
• the structural unit (B) having an ionic group may be a structural unit represented by the structural formula (6) described below.
• the monomer having a carboxy group or a salt thereof, and the ester of a monomer having a carboxy group may be any monomer that is copolymerizable with a vinyl ester monomer and that has a carboxy group or a salt thereof in the vinyl alcohol polymer after saponification.
• Such monomers include acrylic acid or a salt thereof; acrylic acid esters such as methyl acrylate, ethyl acrylate, n-propyl acrylate, and isopropyl acrylate; methacrylic acid or a salt thereof; methacrylic acid esters such as methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, and isopropyl methacrylate; maleic acid or a salt thereof; monomethyl maleate, maleic acid, and the like.
• carboxylic acid ester examples include dimethyl maleate, monoethyl maleate, diethyl maleate, and other maleic acid esters; itaconic acid or a salt thereof; itaconic acid esters such as monomethyl itaconate, dimethyl itaconate, monoethyl itaconate, diethyl itaconate, and other fumaric acid esters; fumaric acid or a salt thereof; fumaric acid esters such as monomethyl fumarate, dimethyl fumarate, monoethyl fumarate, diethyl fumarate, and other fumaric acid esters; maleic anhydride, itaconic anhydride, and a derivative thereof; formyl carboxylic acid such as phthalaldehyde acid, isophthalaldehyde acid, terephthalaldehyde acid, glyoxylic acid, formylacetic acid, and formylpropanoic acid, and other salts thereof.
• formyl carboxylic acid such as
• methyl acrylate, acrylic acid, maleic acid, monomethyl maleate, dimethyl maleate, itaconic acid, monomethyl itaconate, phthalaldehyde acid, isophthalaldehyde acid, terephthalaldehyde acid, glyoxylic acid, or a salt thereof is preferred, and methyl acrylate, acrylic acid, or a salt thereof is more preferred.
• the monomer having a sulfo group or a salt thereof is not particularly limited, and examples thereof include unsaturated sulfonic acids such as vinyl sulfonic acid, allyl sulfonic acid, (meth)acrylic sulfonic acid, styrene sulfonic acid, benzaldehyde sulfonic acid (orthobenzaldehyde sulfonic acid, methabenzaldehyde sulfonic acid, parabenzaldehyde sulfonic acid), 2-acrylamido-2-phenylpropanesulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid (AMPS), or salts of these unsaturated sulfonic acids; unsaturated disulfonic acids such as benzaldehyde-2,4-disulfonic acid, or salts of these unsaturated disulfonic acids
• These monomers having a sulfo group or a salt thereof may be used alone or in combination of two or more.
• orthobenzaldehydesulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid (AMPS), benzaldehyde-2,4-disulfonic acid, or a salt thereof is preferred, and benzaldehydesulfonic acid or a salt thereof is more preferred.
• Examples of monomers having an amino group or a salt thereof include those having an amino group (-NH 2 ) or a salt thereof, a methylamino group (-NHCH 3 ) or a salt thereof, a dimethylamino group (-N(CH 3 ) 2 ) or a salt thereof, a diethylamino group (-N(CH 2 CH 3 ) 2 ) or a salt thereof, and a diphenylamino group (-NPh 2 ) or a salt thereof, and examples thereof include unsaturated amines or salts thereof such as vinyldimethylamine, vinyldiethylamine, vinyldiphenylamine, allyldimethylamine, and methacryldiethylamine. These monomers having an amino group or a salt thereof may be used alone or in combination of two or more. Of these, vinyldimethylamine is preferred from the viewpoint of industrial availability.
• quaternary ammonium group refers to a cation formed by four carbon atoms bonded to one nitrogen atom. However, the four carbon atoms do not necessarily have to be different carbon atoms, and may be the same carbon atom.
• the monomer having a salt of a quaternary ammonium group is not particularly limited as long as it has a salt of a quaternary ammonium group such as quaternary ammonium chloride (-N+(CH 3 ) 3 Cl-), and examples thereof include 3-(methacrylamide)propyltrimethylammonium chloride (MAPTAC).
• the structural unit (B) having an ionic group may be a structural unit represented by the following structural formula (6).
• * represents a bond linking to an adjacent structural unit.
• R5 is an ionic group.
• the ionic group is preferably the above-mentioned ionic group, and more preferably a carboxy group or a salt thereof.
• the vinyl alcohol polymer according to the present invention preferably contains a structural unit (C) having a hydrophobic group made of a hydrocarbon having 3 or more carbon atoms.
• the vinyl alcohol polymer according to the present invention contains a structural unit (C) having a hydrophobic group composed of a hydrocarbon having 3 or more carbon atoms, and therefore when left standing, physical crosslinks are formed by interaction between the hydrophobic groups, thereby improving the viscosity. Furthermore, when shear stress is applied by stirring or the like, the physical crosslinks are temporarily removed, resulting in a decrease in viscosity. As a result, the vinyl alcohol polymer according to the present invention exhibits thixotropy.
• the structural unit (C) include a structural unit represented by the following structural formula (4) and a structural unit represented by the following structural formula (5).
• R2 is a hydrophobic group made of a hydrocarbon having 3 or more carbon atoms, and is preferably an alkyl or alkenyl group having 3 or more carbon atoms.
• R3 is hydrogen or a methyl group.
• the number of carbon atoms in the alkyl or alkenyl group is preferably 3 to 25. When the number of carbon atoms is 3 or more, thixotropy is well exhibited. When the number of carbon atoms is 25 or less, the vinyl alcohol polymer is well soluble in water.
• the alkyl or alkenyl group more preferably has 4 to 25 carbon atoms, further preferably has 6 to 20 carbon atoms, further preferably has 6 to 12 carbon atoms, and further preferably has 10 to 12 carbon atoms.
• the carbon number of the alkyl group or alkenyl group may be linear or branched, but from the above viewpoint, linear is preferable.
• the alkyl group is preferably a hexyl group, an octyl group, a decyl group, a dodecyl group, or the like.
• R 2 is the same as R 2 in the structural formula (4).
• the structural formula (5) can be produced by binding an aldehyde or a derivative thereof to two hydroxyl groups bonded to two carbon atoms bonded to both ends of a methylene group in a vinyl alcohol polymer.
• the carbon number of the aldehyde or derivative thereof is preferably 4 to 20. When the carbon number is 4 or more, thixotropy is well expressed. When the carbon number is 20 or less, the vinyl alcohol polymer dissolves well in water. From this viewpoint, the carbon number is more preferably 4 to 16, even more preferably 6 to 14, and even more preferably 10 to 12.
• the aldehyde is preferably 1-butanal, isobutyraldehyde, tert-butyraldehyde, pentanal, 3-methyl-butanal, 1-hexanal, 1-heptanal, 1-octanal, 2-ethylhexanal, 1-nonanal, 1-decanal, 3,7-dimethyl-1-octanal, 1-undecanal, 1-dodecanal, 3-methyl-3-butenal, citral, citronellal, 7-octenal, and more preferably at least one selected from dodecanal, decanal, and hexanal.
• the vinyl alcohol polymer according to the present invention preferably contains a vinyl alcohol monomer unit.
• the vinyl alcohol polymer according to the present invention preferably contains a vinyl ester monomer unit.
• vinyl ester monomer units include vinyl acetate, vinyl formate, vinyl propionate, vinyl caprylate, vinyl versatate, etc. Among them, vinyl acetate is preferred from an industrial viewpoint. These may be used alone or in combination of two or more.
• the vinyl alcohol polymer of the present invention may further have other structural units than the structural unit (A), the structural unit (B), the structural unit (C), the vinyl alcohol monomer unit, and the vinyl ester monomer unit, so long as the effects of the present invention are obtained.
• the structural units are, for example, structural units derived from ethylenically unsaturated monomers copolymerizable with vinyl esters, and structural units that have been post-modified by acetalization or the like.
• Ethylenically unsaturated monomers are, for example, ⁇ -olefins such as ethylene, propylene, n-butene, and isobutylene; vinyl ethers such as methyl vinyl ether and ethyl vinyl ether; vinyl cyanides such as acrylonitrile and methacrylonitrile; vinyl halides such as vinyl chloride and vinyl fluoride; vinylidene halides such as vinylidene chloride and vinylidene fluoride; allyl compounds such as allyl acetate and allyl chloride; and vinyl silyl compounds such as vinyltrimethoxysilane.
• ⁇ -olefins such as ethylene, propylene, n-butene, and isobutylene
• vinyl ethers such as methyl vinyl ether and ethyl vinyl ether
• vinyl cyanides such as acrylonitrile and methacrylonitrile
• vinyl halides such as vinyl chloride and vinyl fluoride
• the content (a) of the structural unit (A) in the vinyl alcohol polymer according to the present invention is preferably 0.1 to 10 mol %. When it is 0.1 mol % or more, the solubility in water is excellent. When it is 10 mol % or less, the effects attributable to the structural units other than the structural unit (A) are excellent. From this viewpoint, the content (a) of the structural unit (A) is more preferably 0.1 to 8.0 mol%, even more preferably 0.1 to 6.0 mol%, still more preferably 1.0 to 6.0 mol%, even more preferably 2.0 to 6.0 mol%, even more preferably 3.0 to 5.5 mol%, and even more preferably 3.0 to 5.0 mol%.
• the content (b) of the structural unit (B) in the vinyl alcohol polymer according to the present invention is preferably 0.1 to 10 mol %. If it is 0.1 mol % or more, the solubility in water when the aqueous solution is prepared is improved, and when the pH of the aqueous solution is lowered, the structural unit (B) reacts with the hydroxyl group in the vinyl alcohol polymer to form a lactone ring structure or is protonated, thereby reducing the viscosity, and therefore the aqueous solution can be smoothly transferred. If it is 10 mol % or less, the effects attributable to the structural units other than the structural unit (B) are excellent.
• the content (b) of the structural unit (B) is more preferably 0.1 to 8.0 mol%, even more preferably 0.1 to 6.0 mol%, still more preferably 1.0 to 6.0 mol%, even more preferably 2.0 to 6.0 mol%, even more preferably 2.0 to 5.5 mol%, and even more preferably 2.0 to 5.0 mol%.
• the content (c) of the structural unit (C) in the vinyl alcohol polymer according to the present invention is preferably 0.1 to 10 mol %. When it is 0.1 mol % or more, the viscosity of the aqueous solution is improved. When it is 10 mol % or less, the effects attributable to the structural units other than the structural unit (C) are excellent. From this viewpoint, the content (c) of the structural unit (C) is more preferably 0.1 to 8.0 mol%, even more preferably 0.5 to 8.0 mol%, still more preferably 1.2 to 8.0 mol%, even more preferably 1.2 to 5.5 mol%, and still more preferably 1.2 to 3.0 mol%.
• the content of vinyl alcohol monomer units in the vinyl alcohol polymer according to the present invention is preferably 60 to 99 mol %. When it is 60 mol % or more, the effect due to water solubility is excellent. When it is 99 mol % or less, the effect due to the constitutional units other than the vinyl alcohol monomer units is excellent. From this viewpoint, the content of vinyl alcohol monomer units is more preferably 65 to 98 mol %, even more preferably 70 to 97 mol %, still more preferably 75 to 97 mol %, and even more preferably 77 to 96 mol %.
• the content of the vinyl ester monomer unit in the vinyl alcohol polymer according to the present invention is preferably 0.01 to 20 mol %. When it is 0.01 mol % or more, the storage stability of the aqueous solution is excellent. When it is 20 mol % or less, the effects attributable to the constituent units other than the vinyl ester monomer unit are excellent. From this viewpoint, the content of the vinyl ester monomer unit is more preferably 0.01 to 12.0 mol%, even more preferably 0.05 to 5.0 mol%, still more preferably 0.05 to 1.0 mol%, and even more preferably 0.05 to 0.5 mol%.
• the vinyl alcohol polymer according to the present invention comprises a structural unit (A) having a lactone ring, a structural unit (B) having an ionic group, and a structural unit (C) having a hydrophobic group composed of a hydrocarbon having 3 or more carbon atoms, It is preferable that the content of the structural unit (A) relative to all structural units of the vinyl alcohol-based polymer is (a), the content of the structural unit (B) is (b), the content of the structural unit (C) is (c), the number of carbon atoms of the hydrophobic group in the structural unit (C) is (d), and the number of ionic groups in the structural unit (B) is (e), and the following formula (3) is satisfied. 5 ⁇ (c ⁇ (d-3) 2 )/(a+b ⁇ e) ⁇ 95 (3)
• the number of carbon atoms (d) of the hydrophobic group in the structural unit (C) is the sum of the numbers of carbon atoms contained in R 1 and R 2 in structural formula (4), and d is the sum of the number of carbon atoms in R 2 and the number of carbon atoms in the acetal moiety in structural formula (5).
• the numerator “(c ⁇ (d ⁇ 3) 2 )” is an index showing the magnitude of interaction between hydrophobic groups in the resin
• the denominator “(a+b ⁇ e)” is an index showing the solubility in water. Therefore, the middle part “(c ⁇ (d ⁇ 3) 2 )/(a+b ⁇ e)” is an index showing the balance between hydrophobicity and hydrophilicity.
• the middle side "(c ⁇ (d ⁇ 3) 2 )/(a+b ⁇ e)" is more preferably 6 to 70, even more preferably 10 to 60, even more preferably 10 to 55, even more preferably 13 to 55, even more preferably 15 to 55, even more preferably 15 to 50, even more preferably 15 to 45, and even more preferably 15 to 40.
• the modification amount of the vinyl alcohol polymer according to the present invention is not particularly limited, but is preferably 0 to 30.0 mol%. When it is 30.0 mol% or less, the effect attributable to the vinyl alcohol polymer is excellent. From this viewpoint, the modification amount is more preferably 0 to 20.0 mol%, even more preferably 0 to 15.0 mol%, even more preferably 0 to 10.0 mol%, even more preferably 0 to 8.0 mol%, or may be 0 to 6.0 mol%, or may be 0.1 to 8.0 mol%, even more preferably 0.1 to 6.0 mol%, and even more preferably 1.0 to 6.0 mol%.
• the degree of polymerization of the vinyl alcohol polymer according to the present invention is not particularly limited, but is preferably 100 to 5,000. When it is 100 or more, the aqueous solution viscosity is excellent. When the degree of polymerization is 5,000 or less, it is easy to produce industrially. It is more preferably 200 to 4,500, even more preferably 300 to 4,000, even more preferably 400 to 2,500, even more preferably 500 to 2,500, even more preferably 600 to 2,500, even more preferably 700 to 2,500, even more preferably 700 to 2,000, even more preferably 800 to 1,800, and even more preferably 900 to 1,800.
• the method for producing the vinyl alcohol polymer according to the present invention is not particularly limited, and the polymer can be produced, for example, by the following production method.
• a vinyl alcohol polymer according to the present invention is obtained by polymerizing a vinyl ester monomer and a monomer having an ionic group or an ester thereof, followed by saponification to produce a vinyl alcohol polymer, and then acetalizing the hydroxyl groups in the vinyl alcohol polymer with an aldehyde.
• the hydroxyl groups in the vinyl alcohol polymer are acetalized with an aldehyde, and then the vinyl alcohol polymer is acetalized with an aldehyde having an ionic group, thereby providing an ionic group to the side chain of the vinyl alcohol polymer, thereby obtaining the vinyl alcohol polymer according to the present invention.
• a vinyl ester monomer and a monomer having an ionic group, or the vinyl ester and a monomer having a hydrophobic group, are polymerized and then saponified to obtain the vinyl alcohol polymer according to the present invention.
• a vinyl ester monomer and a monomer having a hydrophobic group are polymerized, and then saponified to obtain the vinyl alcohol polymer according to the present invention.
• Examples of the method for producing a vinyl alcohol polymer include known methods such as bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization. Among them, from the viewpoint of obtaining a polymer with a narrow molecular weight distribution, the bulk polymerization method in which polymerization is performed without a solvent or the solution polymerization method in which polymerization is performed in various organic solvents are preferred. From the viewpoint of not using a solvent or a dispersion medium that may cause a side reaction such as chain transfer, the bulk polymerization method is preferred, and from the viewpoint of adjusting the viscosity of the reaction solution and controlling the polymerization rate, the solution polymerization method is preferred.
• organic solvent used in the solution polymerization examples include esters such as methyl acetate and ethyl acetate, aromatic hydrocarbons such as toluene, lower alcohols such as methanol and ethanol, etc. Among these, from the viewpoint of cost, lower alcohols are preferred, and methanol is more preferred.
• the amount of the organic solvent to be added may be selected in consideration of chain transfer of the solvent according to the polymerization degree of the target vinyl alcohol polymer.
• the mass ratio of the organic solvent to the vinyl ester monomer is preferably in the range of 0.01 to 10.
• the mass ratio (organic solvent/vinyl ester monomer) is preferably 0.1 or more and preferably 5 or less.
• a suitable initiator may be selected from conventionally known azo initiators, peroxide initiators, redox initiators, and the like.
• the azo initiator include 2,2'-azobisisobutyronitrile, 2,2'-azobis(2,4-dimethylvaleronitrile), and 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile) (manufactured by Fujifilm Wako Pure Chemical Industries, Ltd., trade name "V-70").
• peroxide initiator examples include percarbonate compounds such as diisopropyl peroxydicarbonate, di-2-ethylhexyl peroxydicarbonate, and diethoxyethyl peroxydicarbonate, perester compounds such as t-butyl peroxyneodecanate, ⁇ -cumyl peroxyneodecanate, and t-butyl peroxyneodecanate, acetylcyclohexylsulfonyl peroxide, diisobutyryl peroxide, and 2,4,4-trimethylpentyl-2-peroxyphenoxyacetate.
• percarbonate compounds such as diisopropyl peroxydicarbonate, di-2-ethylhexyl peroxydicarbonate, and diethoxyethyl peroxydicarbonate
• perester compounds such as t-butyl peroxyneodecanate, ⁇ -cumyl peroxyneodecanate, and
• redox initiators include combinations of the above peroxides with reducing agents such as sodium hydrogen sulfite, sodium hydrogen carbonate, tartaric acid, L-ascorbic acid, and Rongalite.
• reducing agents such as sodium hydrogen sulfite, sodium hydrogen carbonate, tartaric acid, L-ascorbic acid, and Rongalite.
• azo-based initiators are preferred, and 2,2'-azobisisobutyronitrile is more preferred from the viewpoints of polymerization at a relatively low temperature and suppression of side reactions.
• the amount of the initiator to be added varies depending on the polymerization catalyst and cannot be generally determined, but is arbitrarily selected depending on the polymerization rate.
• the amount of the initiator to be added is preferably 0.001 to 1.0 part by mass, more preferably 0.005 to 0.1 part by mass, and even more preferably 0.008 to 0.05 part by mass, based on 100 parts by mass of the raw material monomer of the vinyl alcohol polymer.
• the polymerization temperature is preferably 0°C to 80°C. If the polymerization temperature is 0°C or higher, the polymerization rate is sufficient and productivity is improved. On the other hand, if the polymerization temperature is 80°C or lower, a vinyl alcohol polymer with a narrow molecular weight distribution can be obtained. From this viewpoint, the polymerization temperature is preferably 10 to 80°C, more preferably 20 to 80°C, even more preferably 40 to 70°C, and even more preferably 50 to 70°C.
• the polymerization reaction is terminated by rapidly cooling the reaction system or by adding a polymerization terminator, or by both simultaneously.
• cooling water may be passed through the jacket of the reactor, but a method in which a pre-cooled liquid medium is added to the reactor is preferred.
• the saponification is preferably carried out in a state where the vinyl alcohol polymer before saponification is dissolved in alcohol or aqueous alcohol.
• the alcohol used in the saponification reaction may be a lower alcohol such as methanol or ethanol, and is preferably methanol.
• the alcohol used in the saponification reaction may contain other solvents such as acetone, esters such as methyl acetate and ethyl acetate, and toluene, but the content of other solvents contained in the alcohol is preferably 10% by mass or less, more preferably 5% by mass or less.
• the concentration of the alcohol solution after the addition is preferably 1.0 to 50% by mass, more preferably 5 to 45% by mass, and even more preferably 8 to 40% by mass.
• Examples of the catalyst used in the saponification reaction include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, alkali catalysts such as sodium methylate, and acid catalysts such as mineral acids.
• alkali metal hydroxides such as sodium hydroxide and potassium hydroxide
• alkali catalysts such as sodium methylate
• acid catalysts such as mineral acids.
• sodium hydroxide is preferred from the viewpoint of ease of handling.
• the temperature of the saponification reaction is preferably, for example, 20 to 70° C. If the temperature is 20° C. or higher, the saponification reaction can proceed quickly. When a gel-like product precipitates as the saponification reaction proceeds, it is separated at that point, and the product is crushed, washed, and dried to obtain the vinyl alcohol polymer of the present invention.
• the reaction (acetalization reaction) between vinyl alcohol polymer and aldehyde can be carried out by a known method.
• aqueous medium method in which an aqueous solution of vinyl alcohol polymer and aldehyde are acetalized in the presence of an acid catalyst to precipitate particles of acetalized vinyl alcohol polymer
• a solvent method in which a vinyl alcohol polymer is dispersed in an organic solvent, acetalized with aldehyde in the presence of an acid catalyst, and water or the like, which is a poor solvent for vinyl alcohol polymer, is mixed with the resulting reaction mixture to precipitate acetalized vinyl alcohol polymer
• a method in which a vinyl alcohol polymer is dispersed in an organic solvent, acetalized with aldehyde in the presence of an acid catalyst to obtain an acetalized vinyl alcohol polymer.
• the acid catalyst is not particularly limited, and examples thereof include organic acids such as acetic acid and p-toluenesulfonic acid; inorganic acids such as nitric acid, sulfuric acid and hydrochloric acid; gases that exhibit acidity when dissolved in an aqueous solution, such as carbon dioxide; and solid acid catalysts such as cation exchange resins and metal oxides.
• the aqueous solution of the vinyl alcohol polymer according to the present invention contains the above-mentioned vinyl alcohol polymer and water. Since the aqueous solution of the vinyl alcohol polymer according to the present invention contains the above-mentioned vinyl alcohol polymer, it is possible to easily change the viscosity greatly.
• the content of the vinyl alcohol polymer in the aqueous solution of the vinyl alcohol polymer according to the present invention is preferably 0.1 to 10 mass%, more preferably 0.5 to 5.0 mass%, even more preferably 1.0 to 4.0 mass%, and still more preferably 1.3 to 3.0 mass%.
• the water content in the aqueous solution is preferably 80% by mass or more, and more preferably 90% by mass or more.
• the aqueous solution may contain a pH adjuster. As the pH adjuster, those mentioned above are suitable.
• the suitable pH range of the aqueous solution varies depending on the application, but is preferably 1-14, more preferably 3-12, and even more preferably 4-10.
• the aqueous solution may further contain additives such as surfactants, various plasticizers, antifoaming agents, ultraviolet absorbers, fillers, and water-resistant agents, within the scope of the present invention.
• An aqueous solution of a vinyl alcohol polymer according to one embodiment of the present invention has a vinyl alcohol polymer content of 1 to 3 mass%, a pH of 7 or more at 20° C., and an aqueous solution viscosity of 20 to 1,000,000 cp at a shear rate of 1 [1/s] at 20° C.
• an aqueous solution of a vinyl alcohol-based polymer according to another embodiment of the present invention has a vinyl alcohol-based polymer content of 1 to 3 mass%, a pH of less than 7 at 20°C, and an aqueous solution viscosity of 20 to 100,000 cp at a shear rate of 1 [1/s] at 20°C.
• the coating material according to the present invention contains the above-mentioned vinyl alcohol polymer and water.
• the cement admixture according to the present invention contains the above-mentioned vinyl alcohol polymer and water.
• the paint according to the present invention may further contain other components, if necessary, in addition to the vinyl alcohol polymer and water.
• the other components are not particularly limited, and examples thereof include water-based emulsion resins, pigments, curing catalysts, crosslinking agents, fillers, defoamers, matting agents, crosslinking reaction catalysts, antiskinning agents, dispersants, wetting agents, surfactants, light stabilizers, antifungal agents, antialgae agents, anti-yellowing agents, reducing agents, UV absorbers, freeze stabilizers, antioxidants, film-forming assistants, organic solvents, rust inhibitors, plasticizers, antistatic agents, lubricants, deodorants, preservatives, and charge regulators. These may be used alone or in combination of two or more.
• the content of the vinyl alcohol polymer can be set as desired depending on the physical properties required for the paint. It is not particularly limited, but is preferably 0.001 to 10 mass%.
• the content of the pigment is not particularly limited, but the mass ratio of the pigment to the resin solids of the paint (PWC) is preferably 1 to 70 mass%.
• the coating material according to the present invention can be applied by a suitable method depending on the application and the material to be coated.
• Application methods include, but are not limited to, flow coating, spraying, brushing, flexographic printing, dip coating, spin coating, roll coating, casting, screen printing, and gravure printing.
• the coating is dried to remove the volatiles, resulting in a coating film.
• ultraviolet irradiation treatment or heating treatment at a temperature of about 40 to 120°C may be performed as necessary.
• the aforementioned substrate to be coated is not particularly limited as long as a coating film can be formed on its surface, and may be either an inorganic or organic substrate.
• Substrate materials include, but are not limited to, organic substrates such as natural resins and synthetic resins; and inorganic substrates such as ceramics, metals, glass, stone, concrete, and cement. These may be used alone or in combination of two or more.
• the temperature of the reactor was started to be raised, and when it reached 60°C, 0.06 parts by mass of 2,2'-azobis(isobutyronitrile) (AIBN) was added to start polymerization.
• AIBN 2,2'-azobis(isobutyronitrile)
• the prepared methanol solution of methyl acrylate was dropped into the system to keep the monomer composition (molar ratio of vinyl acetate to methyl acrylate) in the polymerization solution constant.
• the polymerization was terminated when the polymerization rate of vinyl acetate reached 30 mol%.
• the modification amount of the comonomer of the vinyl alcohol polymer obtained in Synthesis Examples 1 and 2 can be determined, for example, by using 1 H-NMR.
• the modification amount can be determined by measuring the vinyl ester polymer, which is a precursor of the vinyl alcohol polymer, by 1 H-NMR.
• the vinyl ester polymer (0.05 g) which is a precursor of PVOH-A, was dissolved in chloroform-d (0.95 g) and subjected to 500 MHz 1 H-NMR measurement.
• the modification amount was calculated from the integral value of the peak (4.7-5.1 ppm) derived from the main chain methine proton of the vinyl ester monomer unit and the peak (3.6-3.7 ppm) derived from the side chain methyl group of methyl acrylate.
• the vinyl ester polymer (0.05 g) which is a precursor of PVOH-B, was dissolved in dimethyl sulfoxide-d6 (0.95 g) and subjected to 500 MHz 1 H-NMR measurement.
• the amount of modification was calculated from the integral values of the peak (4.5-5.0 ppm) derived from the main chain methine proton of the vinyl ester monomer unit and the peak (3.0-3.2 ppm) derived from the side chain methylene group of itaconic acid.
• the amount of modification corresponds to the content of the structural unit consisting of the comonomer relative to the total structural units constituting the vinyl alcohol polymer (a).
• the NMR analysis may be combined with measurements under various temperature conditions and nuclides, or measurements using additives, in order to clarify the structure of the target product.
• the vinyl ester monomer unit content of the vinyl alcohol polymer obtained in Synthesis Examples 1 and 2 can be determined, for example, by 1 H-NMR.
• the vinyl alcohol polymer obtained in Synthesis Examples 1 and 2 (0.05 g) was dissolved in dimethyl sulfoxide-d6 (0.95 g) and subjected to 500 MHz 1 H-NMR measurement. From the obtained 1 H-NMR spectrum, the content of the vinyl ester monomer unit relative to all the constituent units constituting the vinyl alcohol polymer (a) was determined using the peak (1.9-2.0 ppm) derived from the methyl proton of the side chain of the vinyl ester monomer unit.
• the NMR analysis may be combined with measurements under various temperature conditions and nuclides, or measurements using additives, in order to clarify the structure of the target product.
• ⁇ Degree of Polymerization> The viscosity average degree of polymerization is measured in accordance with JIS K 6726-1994.
• the obtained vinyl alcohol polymer is resaponified and purified, and then the intrinsic viscosity [ ⁇ ] (unit: deciliter/g) is measured in water at 30° C. to determine the viscosity average degree of polymerization.
• Example 1 56.7 parts by mass of methanol and 0.6 parts by mass of dodecanal were added to a three-necked flask equipped with a reflux condenser and a thermometer at room temperature (20°C), and 10 parts by mass of PVOH-A obtained in Synthesis Example 1 was added over 1 minute while stirring with a mechanical stirrer. 1.3 parts by mass of p-toluenesulfonic acid was added to the reaction solution, and the temperature was raised to 65°C and the reaction was carried out for 5 hours. 1.7 parts by mass of an 8 mol/L aqueous sodium hydroxide solution was added, and the reaction was carried out at 65°C for 2 hours.
• Example 2 A vinyl alcohol polymer (X), "PVOH-2", was obtained in the same manner as in Example 1, except that the amounts of methanol, dodecanal, p-toluenesulfonic acid, and 8 mol/L aqueous sodium hydroxide solution were changed. The respective conditions are shown in Table 2.
• Example 3 A vinyl alcohol polymer (X), "PVOH-3", was obtained in the same manner as in Example 1, except that the amount of methanol added, 0.8 parts by mass of decanal were added instead of dodecanal, and the amount of 8 mol/L aqueous sodium hydroxide solution added was changed. The respective conditions are shown in Table 2.
• Example 4 A vinyl alcohol polymer (X), "PVOH-4", was obtained in the same manner as in Example 3, except that the amount of decanal added was changed. The conditions are shown in Table 2.
• Example 5 A vinyl alcohol polymer (X) "PVOH-5" was obtained in the same manner as in Example 2, except that the amount of methanol added was 1.6 parts by mass of hexanal instead of dodecanal. The respective conditions are shown in Table 2.
• Example 6 The same method as in Example 1 was used to obtain "PVOH-6", which would become the vinyl alcohol polymer (X), except that the amount of dodecanal added, the amount of PVOH-B obtained in Synthesis Example 2 was added instead of PVOH-A, the amount of p-toluenesulfonic acid added, and the amount of 8 mol/L aqueous sodium hydroxide solution added were changed.
• the respective conditions are shown in Table 2.
• Example 7 The same method as in Example 1 was used to obtain "PVOH-7", which is to become a vinyl alcohol polymer (X), except that the amount of methanol added, 0.9 parts by mass of sodium benzaldehyde sulfonate was added instead of dodecanal, PVOH-C obtained in Synthesis Example 3 was added instead of PVOH-A, the amount of p-toluenesulfonic acid added, and the amount of 8 mol/L aqueous sodium hydroxide solution added were changed. The respective conditions are shown in Table 2.
• Example 8 Except for changing the amount of hexanal added, the same method as in Example 5 was used to obtain "PVOH-8" which is to become the vinyl alcohol polymer (X). The respective conditions are shown in Table 2.
• Example 4 The same method as in Example 1 was used to obtain "PVOH-12", which would become the vinyl alcohol polymer (X), except that the amount of dodecanal added, the amount of PVOH-D obtained in Synthesis Example 4 was added instead of PVOH-A, the amount of p-toluenesulfonic acid added, and the amount of 8 mol/L aqueous sodium hydroxide solution added were changed.
• the respective conditions are shown in Table 2.
• the "structural unit” means a repeating unit having a functional group
• the structural unit having a lactone ring, the ionic group introduced by acetalization, and the hydrophobic group are also considered to be "1 unit”.
• the structural unit (A) having a lactone ring and the structural unit (B) having an ionic group were calculated in duplicate.
• the lactone ring for example, one unit of a monomer unit having a carboxy group reacts with one unit of a vinyl alcohol monomer unit adjacent thereto to produce one lactone ring unit.
• an acetalized structure is also produced by reacting one unit of an acetal unit with two units of vinyl alcohol monomer units to produce one unit of an acetalized structure. Taking this into consideration, the lactone ring and the acetalized structure were calculated as "2 units" in the vinyl alcohol polymer unit in the denominator.
• Ion-exchanged water was added to the vinyl alcohol polymer (X) or an aqueous solution of the vinyl alcohol polymer (X), and an 8 mol/L aqueous sodium hydroxide solution was added in an amount of 2/3 molar of the structural unit (A) having a lactone ring contained in the vinyl alcohol polymer, and the solution was dissolved by stirring at 95 ° C. to prepare an aqueous solution having a vinyl alcohol polymer (X) content of 1.6% by mass.
• the 1.6% by mass aqueous vinyl alcohol polymer solution was allowed to cool to 20 ° C., and while stirring the aqueous solution using a magnetic stirrer, ion-exchanged water and a 20% by mass aqueous citric acid solution or a 2 mol/L aqueous sodium hydroxide solution were added to prepare a 1.5% by mass aqueous solution having a pH of 4 or 10 at 20 ° C.
• the solution was further stirred at 20 ° C. for 5 minutes.
• the pH was measured using a commercially available pH meter (LAQUA Twin compact pH meter manufactured by Horiba, Ltd.).
• ⁇ Viscosity X, Y> After adjusting the pH to 4 according to the above-mentioned method, the viscosity X of the 1.5% by mass aqueous solution (for viscosity X) after 5 minutes was determined using a rotational rheometer (rheometer Discovery HR-2 manufactured by TA Instruments-Waters LLC) under the following measurement conditions: shear rate: 1.0 [1/s], measurement time: 182 seconds.
• the viscosity Y of a 1.5% by mass aqueous solution (for viscosity Y) after 5 minutes was determined using a rotational rheometer (rheometer Discovery HR-2 manufactured by TA Instruments-Waters LLC) under the following measurement conditions: shear rate: 1.0 [1/s], measurement time: 182 seconds.
• ⁇ Viscosity ratio Y/X> The viscosity ratio Y/X of the viscosities X and Y measured by the above method was scored according to the following criteria. Note that the larger the viscosity ratio Y/X, the easier it is to change the viscosity, and the better the viscosity changeability. 5 points: 50.0 or more 4 points: 10.0 or more and less than 50.0 3 points: 5.0 or more and less than 10.0 2 points: 1.5 or more and less than 5.0 1 point: Less than 1.5
• ⁇ Viscosity ratio Y/Z> The viscosity ratio Y/Z of the viscosities Y and Z measured by the above method was scored according to the following criteria. Note that the larger the viscosity ratio Y/Z, the more the viscosity can be lowered by the shear rate during liquid delivery, and the better the liquid delivery properties. 5 points: 10.0 or more 4 points: 5.0 or more and less than 10.0 3 points: 2.0 or more and less than 5.0 2 points: 1.5 or more and less than 2.0 1 point: Less than 1.5
• the viscosity at this time was rated A when it was 4.0 times or more the viscosity of viscosity X, B when it was 2.5 times or more but less than 4.0 times the viscosity of viscosity X, C when it was 1.5 times or more but less than 2.5 times the viscosity of viscosity X, and D when it was less than 1.5 times the viscosity of viscosity X.
• the results are shown in Table 4.

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