JP2010116548A - Absorptive resin particle, method for producing the same, absorbent containing the same and absorptive article - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an absorptive resin particle which allows an absorptive article, to which the absorptive resin particle is applied, to exhibit excellent absorbing properties while showing a specific absorption rate pattern. <P>SOLUTION: The absorptive resin particle contains a cross-linked polymer (A1) containing a water-soluble vinyl monomer (a1) and/or a hydrolyzable vinyl monomer (a2) and a cross-linking agent (b) as essential constituent units. The cross-linked polymer (A1) shows 14-19 mL/g amount (M1) absorbed after one minute, 26-33 mL/g amount (M2) absorbed after two minutes, 42-50 mL/g amount (M3) absorbed after five minutes and 52-59 mL/g amount (M4) absorbed after ten minutes when measured by a DW (Demand Wettability) method. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to absorbent resin particles, a production method thereof, an absorbent body including the same, and an absorbent article.

  As an absorbent resin particle having an excellent absorption rate, an absorbent resin particle having a structure containing a part or all of a hydrophobic substance inside a crosslinked polymer is known (Patent Document 1).

JP 2005-097569 A

In conventional absorbent resin particles and water-absorbing agents, the absorption rate over time after contact with the liquid to be absorbed (hereinafter referred to as an absorption rate pattern) is not appropriate. Specifically, the conventional absorbent resin particles have an absorption rate pattern (i) early early, medium-term normal, late late, (ii) early late, medium-term normal, late fast (the above-mentioned absorbency of Patent Document 1) Resin particles).
When these absorbent resin particles are applied to absorbent articles (paper diapers, etc.), the absorbent used in absorbent articles is biased in the absorption rate of the absorbent resin depending on the location of the absorbent articles, making the absorbent articles effective In the portion where the liquid to be absorbed cannot be used, the problem of blurring or the like is likely to occur, or the time during which the liquid that has not been absorbed in the entire absorber stays longer.
Specifically, when the absorbent resin particle (i) is used, the liquid is rapidly absorbed after contact with the absorbent resin particle at the site where the liquid to be absorbed comes into contact. The resin particles swell and become gelled, preventing the liquid that is not absorbed from diffusing and absorbing in the absorber, and as a result, the area where the absorbed liquid is in contact has a high absorption rate of the absorbent resin particles, and the other areas are Absorption rate deviation that the absorption rate of the absorbent resin particles is low occurs. And the time for which the liquid which was not absorbed stays in the site | part which the absorbed liquid contacted becomes long.
On the other hand, when the absorbent resin particles of (ii) are used, the liquid is only gradually absorbed after contact with the absorbent resin particles at the site where the liquid to be absorbed comes into contact, and the liquid that is not absorbed in the absorbent article. As a result, the absorptivity of the absorbent resin particles tends to be equal at the site where the absorbed liquid is in contact with the other site. However, the absorption speed is generally slow, and the time during which the liquid that has not been absorbed in the entire absorber stays is increased.
And in the site | part in which the liquid which was not absorbed remains long, the wearer's skin which contacts the site | part tends to produce problems, such as a blurring.
Therefore, an absorbent article that does not have such problems as fogging and an absorbent resin particle that can be used therefor are strongly desired.
That is, an object of the present invention is to provide absorbent resin particles having a specific absorption rate pattern.

  The absorbent resin particle of the present invention comprises a water-soluble vinyl monomer (a1) and / or a hydrolyzable vinyl monomer (a2), and a crosslinked polymer (A1) having a crosslinking agent (b) as essential constituent units. Absorbent resin particles having an absorption amount (M1) after 1 minute according to DW (Demand Wetability) method of (A1) of 14 to 19 ml / g, and an absorption amount after 2 minutes (M2) of 26 to 33 ml The absorption amount after 5 minutes (M3) is 42 to 50 ml / g, and the absorption amount after 10 minutes (M4) is 52 to 59 ml / g.

  The gist of the absorbent body of the present invention is that it comprises the above-described absorbent resin particles and a fibrous material.

  The gist of the absorbent article of the present invention is that the absorbent article is provided.

The method for producing absorbent resin particles of the present invention comprises a hydrophobic substance (C), a water-soluble vinyl monomer (a1) and / or a hydrolyzable vinyl monomer (a2), and an internal crosslinking agent (b) as essential constituent units. Mixing or kneading with the hydrogel of the crosslinked polymer (A1) to be performed; and / or in the presence of the hydrophobic substance (C), the water-soluble vinyl monomer (a1) and / or the hydrolyzable vinyl monomer (a2) and A method for producing absorbent resin particles comprising a step of polymerizing an internal crosslinking agent (b) as an essential constituent unit to obtain a hydrogel of a crosslinked polymer (A1),
The weight average particle diameter (μm) of the absorbent resin particles is 400 to 650, the apparent density (g / ml) of the absorbent resin particles is 0.56 to 0.62, and the DW (Demand) of the absorbent resin particles The absorption amount (M1) after 1 minute according to the Wettability method is 14 to 19 ml / g, the absorption amount after 2 minutes (M2) is 26 to 33 ml / g, and the absorption amount (M3) after 5 minutes is It is 42 to 50 ml / g, and the summary is that the absorbed amount (M4) after 10 minutes is 52 to 59 ml / g.

The absorbent resin particles of the present invention and the absorbent resin particles obtained by the production method of the present invention have a specific absorption rate pattern.
Therefore, when the absorbent resin particles of the present invention are applied to absorbent articles (paper diapers, sanitary napkins, etc.), there is no bias in absorptivity, and excellent absorption performance (absorption amount and absorption speed) is exhibited. Hard to occur.

It is the figure which represented typically the apparatus for measuring the amount of absorption by DW method.

  The water-soluble vinyl monomer (a1) is not particularly limited and is known {for example, a vinyl monomer disclosed in Japanese Patent No. 3648553, Japanese Patent Laid-Open No. 2003-165883, Japanese Patent Laid-Open No. 2005-75982, Japanese Patent Laid-Open No. 2005-95759}. Etc. can be used.

  The hydrolyzable vinyl monomer (a2) means a vinyl monomer that becomes a water-soluble vinyl monomer (a1) by hydrolysis, and is not particularly limited (for example, Japanese Patent No. 3648553, JP-A No. 2003-165883, The vinyl monomer etc. of Unexamined-Japanese-Patent No. 2005-75982, Unexamined-Japanese-Patent No. 2005-95759} etc. can be used. The water-soluble vinyl monomer means a vinyl monomer having a property of dissolving at least 100 g in 100 g of water at 25 ° C. The term “hydrolyzable” refers to the property of being hydrolyzed by the action of 50 ° C. water and, if necessary, the catalyst (acid or base) to make it water-soluble. Hydrolysis of the hydrolyzable vinyl monomer may be performed either during polymerization, after polymerization, or both of them, but from the viewpoint of the molecular weight of the resulting absorbent resin particles, etc., is preferable.

  Of these, water-soluble vinyl monomers (a1) are preferred from the viewpoint of absorption characteristics, etc., more preferably anionic vinyl monomers, and more preferably carboxy (salt) groups, sulfo (salt) groups, amino groups, carbamoyl groups. Vinyl monomers having an ammonio group or a mono-, di- or tri-alkyl ammonio group, then preferably vinyl monomers having a carboxy (salt) group or a carbamoyl group, particularly preferably (meth) acrylic acid (salt) and (Meth) acrylamide, next particularly preferably (meth) acrylic acid (salt), most preferably acrylic acid (salt).

The “carboxy (salt) group” means “carboxy group” or “carboxylate group”, and the “sulfo (salt) group” means “sulfo group” or “sulfonate group”. Moreover, (meth) acrylic acid (salt) means acrylic acid, acrylate, methacrylic acid or methacrylate, and (meth) acrylamide means acrylamide or methacrylamide. Examples of the salt include an alkali metal (such as lithium, sodium and potassium) salt, an alkaline earth metal (such as magnesium and calcium) salt or an ammonium (NH ₄ ) salt. Among these salts, alkali metal salts and ammonium salts are preferable from the viewpoint of absorption characteristics and the like, more preferably alkali metal salts, and particularly preferably sodium salts.

  When either the water-soluble vinyl monomer (a1) or the hydrolyzable vinyl monomer (a2) is used as a structural unit, each may be used alone as a structural unit, or two or more kinds may be used as a structural unit if necessary. The same applies when the water-soluble vinyl monomer (a1) and the hydrolyzable vinyl monomer (a2) are used as constituent units. Further, when the water-soluble vinyl monomer (a1) and the hydrolyzable vinyl monomer (a2) are used as structural units, the content molar ratio (a1 / a2) is preferably 75/25 to 99/1, more preferably. 85/15 to 95/5, particularly preferably 90/10 to 93/7, and most preferably 91/9 to 92/8. Within this range, the absorption performance is further improved.

  As a structural unit of the absorbent resin particles, in addition to the water-soluble vinyl monomer (a1) and the hydrolyzable vinyl monomer (a2), other vinyl monomers (a3) copolymerizable therewith can be used as the structural unit. .

Other vinyl monomers (a3) that can be copolymerized are not particularly limited and are known {for example, Japanese Patent No. 3648553, Japanese Patent Application Laid-Open No. 2003-165883, Japanese Patent Application Laid-Open No. 2005-75982, Japanese Patent Application Laid-Open No. 2005-95759. } Can be used, and the following vinyl monomers (i) to (iii) can be used.
(I) C8-C30 aromatic ethylenic monomer Styrene such as styrene, α-methylstyrene, vinyltoluene and hydroxystyrene, and halogen substituted products of styrene such as vinylnaphthalene and dichlorostyrene.
(Ii) C2-C20 aliphatic ethylene monomer Alkene [ethylene, propylene, butene, isobutylene, pentene, heptene, diisobutylene, octene, dodecene, octadecene, etc.]; and alkadiene [butadiene, isoprene, etc.], etc.
(Iii) C5-C15 alicyclic ethylene monomer Monoethylenically unsaturated monomer [pinene, limonene, indene and the like]; and polyethylene vinyl polymerizable monomer [cyclopentadiene, bicyclopentadiene, ethylidene norbornene and the like] and the like.

  When the other vinyl monomer (a3) is used as a constituent unit, the content (mol%) of the other vinyl monomer (a3) unit is that of the water-soluble vinyl monomer (a1) unit and the hydrolyzable vinyl monomer (a2) unit. Based on the number of moles, 0.01 to 5 is preferable, more preferably 0.05 to 3, then preferably 0.08 to 2, and particularly preferably 0.1 to 1.5. From the viewpoint of absorption characteristics and the like, the content of other vinyl monomer (a3) units is most preferably 0 mol%.

There are no particular limitations on the crosslinking agent (b), and known crosslinking agents such as those disclosed in known {eg, Japanese Patent No. 3648553, Japanese Patent Laid-Open No. 2003-165883, Japanese Patent Laid-Open No. 2005-75982, Japanese Patent Laid-Open No. 2005-95759}, and the like. Can be used.
Among these, from the viewpoint of absorption characteristics, etc., a crosslinking agent having two or more ethylenically unsaturated groups is preferable, more preferably a poly (meth) allyl ether of a polyol having 2 to 10 carbon atoms, particularly preferably triallylsia. Nurate, triallyl isocyanurate, tetraallyloxyethane and pentaerythritol triallyl ether, most preferably pentaerythritol triallyl ether.

  The content (mol%) of the crosslinking agent (b) unit is preferably 0.001 to 5, more preferably, based on the number of moles of the water-soluble vinyl monomer (a1) unit and the hydrolyzable vinyl monomer (a2) unit. Is 0.005 to 3, particularly preferably 0.01 to 1. Within this range, the absorption characteristics are further improved.

  The cross-linked polymer (A1) may be one type or a mixture of two or more types.

  The cross-linked polymer (A1) can be prepared by known aqueous solution polymerization {adiabatic polymerization, thin film polymerization, spray polymerization method, etc .; JP-A-55-133413, etc.} or known reverse-phase suspension polymerization {Japanese Examined Patent Publication No. 54-30710. Gazette, JP-A-56-26909 and JP-A-1-5808, etc.}. Among the polymerization methods, the solution polymerization method is preferable, and an aqueous solution polymerization method is particularly preferable because it is not necessary to use an organic solvent and is advantageous in terms of production cost.

  Water-containing gel obtained by polymerization {consists of a crosslinked polymer and water. } Can be shredded as necessary. The size (longest diameter) of the gel after chopping is preferably 50 μm to 10 cm, more preferably 100 μm to 2 cm, and particularly preferably 1 mm to 1 cm. Within this range, the drying property in the drying process is further improved.

  Shredding can be performed by a known method, and can be shredded using a normal shredding device {for example, a bex mill, rubber chopper, pharma mill, mincing machine, impact crusher and roll crusher}. .

  When using a solvent (organic solvent, water, etc.) for the polymerization, it is preferable to distill off the solvent after the polymerization. When the solvent contains an organic solvent, the content (% by weight) of the organic solvent after the distillation is preferably 0 to 10, more preferably 0 to 5, particularly preferably 0, based on the weight of the absorbent resin particles. ~ 3, most preferably 0-1. Within this range, the absorption performance (particularly the water retention amount) of the absorbent resin particles is further improved.

  When water is contained in the solvent, the water content (% by weight) after the distillation is preferably 0 to 20, more preferably 1 to 10, particularly preferably 2 to 9, most preferably based on the weight of the crosslinked polymer. 3-8. Within this range, the absorption performance and the breakability of the absorbent resin particles after drying are further improved.

  In addition, the content and moisture of the organic solvent are an infrared moisture meter {JE400 manufactured by KETT Co., Ltd .: 120 ± 5 ° C., 30 minutes, atmospheric humidity before heating 50 ± 10% RH, lamp specification 100V, 40W } Is obtained from the weight loss of the measurement sample before and after heating.

  As a method of distilling off the solvent (including water), a method of distilling (drying) with hot air at a temperature of 80 to 230 ° C., a thin film drying method using a drum dryer heated to 100 to 230 ° C., (heating ) Vacuum drying, freeze drying, infrared drying, decantation, filtration, etc. can be applied.

  The crosslinked polymer can be pulverized after drying. The pulverization method is not particularly limited, and a normal pulverizer (for example, a hammer-type pulverizer, an impact-type pulverizer, a roll-type pulverizer, and a shet airflow-type pulverizer) can be used. The pulverized crosslinked polymer can be adjusted in particle size by sieving or the like, if necessary.

  The weight average particle diameter (μm) of the crosslinked polymer (A1) when screened if necessary is preferably 400 to 650, particularly preferably 450 to 600, and most preferably 500 to 540. Within this range, the absorption performance is further improved.

  In addition, the weight average particle diameter was measured using a low-tap test sieve shaker and a standard sieve (JIS Z8801-1: 2006), Perry's Chemical Engineers Handbook, 6th edition (McGlow Hill Book Company, 1984). , Page 21). That is, JIS standard sieves are combined in the order of 1000 μm, 850 μm, 710 μm, 500 μm, 425 μm, 355 μm, 250 μm, 150 μm, 125 μm, 75 μm and 45 μm, and a tray from the top. About 50 g of the measured particles are put in the uppermost screen and shaken for 5 minutes with a low-tap test sieve shaker. Weigh the measured particles on each sieve and the pan, and calculate the weight fraction of the particles on each sieve with the total as 100% by weight. This value is the logarithmic probability paper {the horizontal axis is the sieve aperture (particle size ), The vertical axis is plotted in the weight fraction}, a line connecting the points is drawn, and the particle diameter corresponding to the weight fraction of 50% by weight is obtained, and this is defined as the weight average particle diameter.

  In addition, since the absorption performance is better when the content of fine particles is smaller, the content of fine particles of 106 μm or less (preferably 150 μm or less) in the total particles is preferably 3% by weight or less, more preferably 1% by weight or less. It is. The content of the fine particles can be determined using a plot created when determining the above weight average particle diameter.

The apparent density (g / ml) of the crosslinked polymer (A1) is preferably 0.56 to 0.62, more preferably 0.57 to 0.61, and particularly preferably 0.58 to 0.60. Within this range, the absorption performance is further improved.
The apparent density is measured at 25 ° C. according to JIS K7365: 1999.

  The shape of the crosslinked polymer (A1) is not particularly limited, and examples thereof include an irregular crushed shape, a flake shape, a pearl shape, and a rice grain shape. Among these, from the viewpoint of good entanglement with the fibrous material in the use of paper diapers and the like and no fear of dropping off from the fibrous material, an irregular crushed shape is preferable.

  The crosslinked polymer (A1) can be subjected to a surface crosslinking treatment with a surface crosslinking agent, if necessary. As the surface cross-linking agent, known {Japanese Patent Laid-Open Nos. 59-189103, 58-180233, 61-16903, 61-21305, 61-252212 are known. , JP-A-51-136588, JP-A-61-257235, etc.} surface crosslinking agent {polyvalent glycidyl, polyhydric alcohol, polyvalent amine, polyvalent aziridine, polyvalent isocyanate, silane coupling Agents and polyvalent metals, etc.} can be used. Of these surface cross-linking agents, from the viewpoint of economy and absorption properties, polyvalent glycidyl, polyhydric alcohol and polyvalent amine are preferable, more preferably polyvalent glycidyl and polyhydric alcohol, particularly preferably polyvalent glycidyl, most preferably Preferred is ethylene glycol diglycidyl ether.

  In the case of surface cross-linking treatment, the amount (% by weight) of the surface cross-linking agent is not particularly limited because it can be variously changed depending on the type of surface cross-linking agent, the conditions for cross-linking, the target performance, etc. From the viewpoint of the above, based on the weight of the water-soluble vinyl monomer (a1), the hydrolyzable vinyl monomer (a2) and the crosslinking agent (b), 0.001 to 3 is preferable, more preferably 0.005 to 2, Most preferably, it is 0.01-1.

  In the case of performing the surface cross-linking treatment, the method of the surface cross-linking treatment is known {for example, the method of Japanese Patent No. 3648553, JP-A No. 2003-165883, JP-A No. 2005-75982, JP-A No. 2005-95759}. Is applicable.

  The hydrophobic substance (C) includes a hydrophobic substance (C1) containing a hydrocarbon group, a hydrophobic substance (C2) containing a hydrocarbon group having a fluorine atom, and a hydrophobic substance (C3) having a polysiloxane structure. Etc. are included.

  Hydrophobic substances (C1) containing hydrocarbon groups include polyolefin resins, polyolefin resin derivatives, polystyrene resins, polystyrene resin derivatives, waxes, long chain fatty acid esters, long chain fatty acids and salts thereof, long chain aliphatic alcohols and these Or a mixture of two or more thereof.

  As the polyolefin resin, an olefin having 2 to 4 carbon atoms {ethylene, propylene, isobutylene, isoprene, etc.} as an essential constituent monomer (the olefin content is at least 50% by weight based on the weight of the polyolefin resin) And polymers having an average molecular weight of 1,000 to 1,000,000 {for example, polyethylene, polypropylene, polyisobutylene, poly (ethylene-isobutylene), isoprene, etc.}.

  Examples of the polyolefin resin derivative include polymers having a weight average molecular weight of 1,000 to 1,000,000 introduced by introducing a carboxyl group (—COOH), 1,3-oxo-2-oxapropylene (—COOCO—) or the like into a polyolefin resin {for example, polyethylene heat Degradation, polypropylene thermal degradation, maleic acid modified polyethylene, chlorinated polyethylene, maleic acid modified polypropylene, ethylene-acrylic acid copolymer, ethylene-maleic anhydride copolymer, isobutylene-maleic anhydride copolymer, maleation Polybutadiene, ethylene-vinyl acetate copolymer, and maleated product of ethylene-vinyl acetate copolymer}.

  As the polystyrene resin, a polymer having a weight average molecular weight of 1,000 to 1,000,000 can be used.

  As the polystyrene resin derivative, a polymer having a weight average molecular weight of 1,000 to 1,000,000 (for example, styrene-containing styrene as an essential constituent monomer (the content of styrene is at least 50% by weight based on the weight of the polystyrene derivative)). Maleic anhydride copolymer, styrene-butadiene copolymer, styrene-isobutylene copolymer, etc.}.

  Examples of the wax include waxes having a melting point of 50 to 200 ° C. (for example, paraffin wax, beeswax, carbana wax, beef tallow, etc.).

  As long-chain fatty acid esters, esters of fatty acids having 8 to 25 carbon atoms and alcohols having 1 to 12 carbon atoms {for example, methyl laurate, ethyl laurate, methyl stearate, ethyl stearate, methyl oleate, oleic acid Ethyl, glycerin lauric acid monoester, glycerin stearic acid monoester, glycerin oleic acid monoester, pentaerythritol lauric acid monoester, pentaerythritol stearate monoester, pentaerythritol oleic acid monoester, sorbit lauric acid monoester, Sorbit stearic acid monoester, sorbit oleic acid monoester, sucrose palmitic acid monoester, sucrose palmitic acid diester, sucrose palmitic acid triester, sucrose stearic acid monoester Ester, sucrose stearic acid diester, sucrose stearic acid triester, and beef tallow} and the like. Of these, sucrose stearate monoester, sucrose stearate diester, and sucrose stearate triester are preferable from the viewpoint of the resistance to moisture of the absorbent article, and more preferably sucrose stearate monoester and sucrose. Stearic acid diester.

  Examples of long chain fatty acids and salts thereof include fatty acids having 8 to 25 carbon atoms (for example, lauric acid, palmitic acid, stearic acid, oleic acid, dimer acid, and behenic acid). Examples of the salt include salts with calcium, magnesium, or aluminum (hereinafter abbreviated as Ca, Mg, Al) {for example, palmitic acid Ca, palmitic acid Al, stearic acid Ca, stearic acid Mg, stearic acid Al, etc.}. From the viewpoint of the moisture resistance of the absorbent article, Ca stearate, Mg stearate, and Al stearate are preferred, and Mg stearate is more preferred.

  Examples of the long-chain aliphatic alcohol include aliphatic alcohols having 8 to 25 carbon atoms (for example, lauryl alcohol, palmityl alcohol, stearyl alcohol, oleyl alcohol, etc.). From the viewpoint of the moisture resistance of the absorbent article, palmityl alcohol, stearyl alcohol, and oleyl alcohol are preferable, and stearyl alcohol is more preferable.

  Examples of the mixture of two or more of these include a mixture of a long-chain fatty acid ester and a long-chain aliphatic alcohol {for example, a mixture of sucrose stearic acid diester and stearyl alcohol}.

  Examples of the hydrophobic substance (C2) containing a hydrocarbon group having a fluorine atom include perfluoroalkane, perfluoroalkene, perfluoroaryl, perfluoroalkyl ether, perfluoroalkyl carboxylic acid, perfluoroalkyl alcohol, and those 2 A mixture of seeds or more is included.

  As perfluoroalkanes, alkanes having 4 to 42 fluorine atoms and 1 to 20 carbon atoms {for example, trifluoromethane, pentafluoroethane, pentafluoropropane, heptafluoropropane, heptafluorobutane, nonafluorofluorohexane, tridecafluoro Octane and heptadecafluorododecane, etc.}.

  The perfluoroalkene includes alkenes having 4 to 42 fluorine atoms and 2 to 20 carbon atoms (for example, trifluoroethylene, pentafluoropropene, trifluoropropene, heptafluorobutene, nonafluorofluorohexene, tridecafluorooctene and hepta Decafluorododecene etc.}.

  Perfluoroaryl includes aryl having 4 to 42 fluorine atoms and 6 to 20 carbon atoms (for example, trifluorobenzene, pentafluorotoluene, trifluoronaphthalene, heptafluorobenzene, nonafluorofluoroxylene, tridecafluorooctylbenzene and Heptadecafluorododecylbenzene, etc.}.

  Examples of perfluoroalkyl ether include ethers having 2 to 82 fluorine atoms and 2 to 40 carbon atoms (for example, ditrifluoromethyl ether, dipentafluoroethyl ether, dipentafluoropropyl ether, diheptafluoropropyl ether, diheptafluoro). Butyl ether, dinonafluorofluorohexyl ether, ditridecafluorooctyl ether, diheptadecafluorododecyl ether, etc.}.

  Examples of perfluoroalkylcarboxylic acids include carboxylic acids having 3 to 41 fluorine atoms and 1 to 21 carbon atoms (for example, pentafluoroethanoic acid, pentafluoropropanoic acid, heptafluoropropanoic acid, heptafluorobutanoic acid, nonafluorofluorohexane). Acid, tridecafluorooctanoic acid, heptadecafluorododecanoic acid, and salts of these metals (alkali metal and alkaline earth metal etc.), etc.}.

  Perfluoroalkyl alcohols include alcohols having 3 to 41 fluorine atoms and 1 to 20 carbon atoms (for example, pentafluoroethanol, pentafluoropropanol, heptafluoropropanol, heptafluorobutanol, nonaflufluorohexanol, tridecafluorooctanol and Heptadecafluorododecanol and the like} and ethylene oxide (1 to 20 mol per 1 mol of alcohol) adduct of this alcohol.

  Examples of the mixture of two or more of these include a mixture of perfluoroalkylcarboxylic acid and perfluoroalkyl alcohol {for example, a mixture of pentafluoroethanoic acid and pentafluoroethanol, etc.}.

  Examples of the hydrophobic substance (C3) having a polysiloxane structure include polydimethylsiloxane, polyether-modified polysiloxane {polyoxyethylene-modified polysiloxane and poly (oxyethylene / oxypropylene) -modified polysiloxane, etc.}, carboxy-modified polysiloxane, Epoxy-modified polysiloxane, amino-modified polysiloxane, alkoxy-modified polysiloxane and the like, and mixtures thereof are included.

  The position of the organic group (modified group) of the modified silicone {polyether-modified polysiloxane, carboxy-modified polysiloxane, epoxy-modified polysiloxane, amino-modified polysiloxane, etc.} is not particularly limited, but the side chain of polysiloxane, polysiloxane Both ends of the polysiloxane, one end of the polysiloxane, and both the side chain and both ends of the polysiloxane may be used. Among these, from the viewpoint of absorption characteristics and the like, both the side chain of polysiloxane and the side chain and both ends of polysiloxane are preferred, and both the side chain and both ends of polysiloxane are more preferred.

  Examples of the organic group (modified group) of the polyether-modified polysiloxane include a group containing a polyoxyethylene group or a poly (oxyethylene / oxypropylene) group. The content (pieces) of oxyethylene groups and / or oxypropylene groups contained in the polyether-modified polysiloxane is preferably 2 to 40, more preferably 5 to 30, particularly preferably per molecule of the polyether-modified polysiloxane. 7-20, most preferably 10-15. Within this range, the absorption characteristics are further improved. Moreover, when it contains an oxyethylene group and an oxypropylene group, the content (% by weight) of the oxyethylene group is preferably 1 to 30, more preferably 3 to 25, and particularly preferably 5 based on the weight of the polysiloxane. ~ 20. Within this range, the absorption characteristics are further improved.

The polyether-modified polysiloxane can be easily obtained from the market. For example, the following products {modified position, type of oxyalkylene} can be preferably exemplified.
* Shin-Etsu Chemical Co., Ltd. KF-945 {side chain, oxyethylene and oxypropylene}, KF-6020 {side chain, oxyethylene and oxypropylene}, X-22-6191 {side chain, oxyethylene and oxypropylene} X-22-4922 {side chain, oxyethylene and oxypropylene}, X-22-4272 {side chain, oxyethylene and oxypropylene}, X-22-6266 {side chain, oxyethylene and oxypropylene}

FZ-2110 {both ends, oxyethylene and oxypropylene}, FZ-2122 {both ends, oxyethylene and oxypropylene}, FZ-7006 {both ends, oxyethylene and oxypropylene}, manufactured by Toray Dow Corning Co., Ltd. FZ-2166 {both ends, oxyethylene and oxypropylene}, FZ-2164 {both ends, oxyethylene and oxypropylene}, FZ-2154 {both ends, oxyethylene and oxypropylene}, FZ-2203 {both ends, oxy Ethylene and oxypropylene} and FZ-2207 {both ends, oxyethylene and oxypropylene}

  The organic group (modified group) of the carboxy-modified polysiloxane includes a group containing a carboxy group, and the organic group (modified group) of the epoxy-modified polysiloxane includes a group containing an epoxy group. Examples of the organic group (modified group) of polysiloxane include groups containing amino groups (1, 2, and tertiary amino groups). The organic group (modified group) content (g / mol) of these modified silicones is preferably 200 to 11000, more preferably 600 to 8000, and particularly preferably 1000 to 4000 as carboxy equivalent, epoxy equivalent or amino equivalent. It is. Within this range, the absorption characteristics are further improved. The carboxy equivalent is measured according to “16. Total acid value test” of JIS C2101: 1999. Moreover, an epoxy equivalent is calculated | required based on JISK7236: 2001. The amino equivalent is measured according to “8. Potentiometric titration method (base number / hydrochloric acid method)” of JIS K2501: 2003.

The carboxy-modified polysiloxane can be easily obtained from the market. For example, the following products {modified position, carboxy equivalent (g / mol)} can be preferably exemplified.
* Shin-Etsu Chemical Co., Ltd. X-22-3701E {side chain, 4000}, X-22-162C {both ends, 2300}, X-22-3710 {single end, 1450}

-BY 16-880 {side chain, 3500}, BY 16-750 {both ends, 750}, BY 16-840 {side chain, 3500}, SF8418 {side chain, 3500} manufactured by Toray Dow Corning Co., Ltd.

The epoxy-modified polysiloxane can be easily obtained from the market. For example, the following products {modified position, epoxy equivalent} can be preferably exemplified.
・ X-22-343 {side chain, 525}, KF-101 {side chain, 350}, KF-1001 {side chain, 3500}, X-22-2000 {side chain, 620} manufactured by Shin-Etsu Chemical Co., Ltd. X-22-2046 {side chain, 600}, KF-102 {side chain, 3600}, X-22-4741 {side chain, 2500}, KF-1002 {side chain, 4300}, X-22-3000T {Side chain, 250}, X-22-163 {both ends, 200}, KF-105 {both ends, 490}, X-22-163A {both ends, 1000}, X-22-163B {both ends, 1750}, X-22-163C {both ends, 2700}, X-22-169AS {both ends, 500}, X-22-169B {both ends, 1700}, X-22-173DX {single end, 4500} , X-22-9002 { Side chain, both ends, 5000}

-FZ-3720 {side chain, 1200}, BY 16-839 {side chain, 3700}, SF 8411 {side chain, 3200}, SF 8413 {side chain, 3800}, SF 8421 {manufactured by Toray Dow Corning Co., Ltd. Side chain, 11000}, BY 16-876 {side chain, 2800}, FZ-3736 {side chain, 5000}, BY 16-855D {side chain, 180}, BY 16-8 {side chain, 3700}

The amino-modified silicone can be easily obtained from the market. For example, the following products {modified position, amino equivalent} can be preferably exemplified.
-Shin-Etsu Chemical Co., Ltd. KF-865 {side chain, 5000}, KF-864 {side chain, 3800}, KF-859 {side chain, 6000}, KF-393 {side chain, 350}, KF-860 {Side Chain, 7600}, KF-880 {Side Chain, 1800}, KF-8004 {Side Chain, 1500}, KF-8002 {Side Chain, 1700}, KF-8005 {Side Chain, 11000}, KF-867 {Side Chain, 1700}, X-22-3820W {Side Chain, 55000}, KF-869 {Side Chain, 8800}, KF-861 {Side Chain, 2000}, X-22-3939A {Side Chain, 1500} , KF-877 {side chain, 5200}, PAM-E {both ends, 130}, KF-8010 {both ends, 430}, X-22-161A {both ends, 800}, X-22-161B {both Terminal 1500 }, KF-8012 {both ends, 2200}, KF-8008 {both ends, 5700}, X-22-1660B-3 {both ends, 2200}, KF-857 {side chain, 2200}, KF-8001 { Side chain, 1900}, KF-862 {side chain, 1900}, X-22-9192 {side chain, 6500}

-FZ-3707 {side chain, 1500}, FZ-3504 {side chain, 1000}, BY 16-205 {side chain, 4000}, FZ-3760 {side chain, 1500}, FZ manufactured by Toray Dow Corning Co., Ltd. -3705 {side chain, 4000}, BY 16-209 {side chain, 1800}, FZ-3710 {side chain, 1800}, SF 8417 {side chain, 1800}, BY 16-849 {side chain, 600}, BY 16-850 {side chain, 3300}, BY 16-879B {side chain, 8000}, BY 16-892 {side chain, 2000}, FZ-3501 {side chain, 3000}, FZ-3785 {side chain, 6000}, BY 16-872 {side chain, 1800}, BY 16-213 {side chain, 2700}, BY 16-203 {side chain, 1900}, BY 16-898 {side chain, 2900 BY 16-890 {side chain, 1900}, BY 16-893 {side chain, 4000}, FZ-3789 {side chain, 1900}, BY 16-871 {both ends, 130}, BY 16-853C {both Terminal 360}, BY 16-853U {both ends, 450}

  Examples of these mixtures include a mixture of polydimethylsiloxane and carboxyl-modified polysiloxane, a mixture of polyether-modified polysiloxane and amino-modified polysiloxane, and the like.

The viscosity (mPa · s, 25 ° C.) of the hydrophobic substance having a polysiloxane structure is preferably 10 to 5000, more preferably 15 to 3000, and particularly preferably 20 to 1500. Within this range, the absorption characteristics are further improved. The viscosity is JIS Z8803-1991 “Viscosity of liquid”. Cone and cone-measured according to the viscosity measurement method using a flat plate rotational viscometer {for example, E-type viscometer with temperature adjusted to 25.0 ± 0.5 ° C. (RE80L, Toki Sangyo Co., Ltd., radius 7 mm) , Angle 5.24 × 10 ⁻² rad cone). }

The HLB value of the hydrophobic substance (C) is preferably from 1 to 10, more preferably from 3 to 8, particularly preferably from 5 to 7. Within this range, the moisture resistance of the absorbent article is further improved.
The HLB value means a hydrophilic-hydrophobic balance (HLB) value, and is determined by the Oda method (new introduction to surfactants, page 197, Takehiko Fujimoto, Sanyo Chemical Industries, Ltd., published in 1981). .

  Of these hydrophobic substances (C), from the viewpoint of the resistance to moisture of the absorbent article, a long chain fatty acid ester, a long chain fatty acid salt, a long chain fatty acid alcohol, a hydrophobic substance having a polysiloxane structure is preferable. More preferably sucrose stearate, Mg stearate, stearyl alcohol, amino-modified polysiloxane, carboxy-modified polysiloxane, particularly preferably sucrose stearate monoester, sucrose stearate diester, Mg stearate, stearyl alcohol, amino It is a modified polysiloxane.

  The content (% by weight) of the hydrophobic substance (C) is preferably 0.001 to 5.0, more preferably 0.08 to 1.0, particularly preferably based on the weight of the crosslinked polymer (A1). Is 0.08 to 0.16. This range is preferable because the anti-absorbent article is excellent in anti-fogging property.

  If the absorbent resin particle of the present invention has a structure comprising part or all of the hydrophobic substance (C) inside the absorbent resin particle, how the hydrophobic substance (C) is contained. It does not matter. However, the structure comprising part or all of the hydrophobic substance (C) inside the absorbent resin particles is composed of (C) inside the absorbent resin particles from the viewpoint of the resistance to leakage of the absorbent article. A structure including the connecting portion (RC) is preferable.

The structure including the connecting portion (RC) made of (C) inside the absorbent resin particles will be described.
The connecting portion (RC) is a sandwich composed of (A1)-(C)-(A1) formed by contacting at least half of the total surface area of the hydrophobic substance (C) with the crosslinked polymer (A1). Means structure.
When the hydrophobic substance (C) is present only on the surface of the absorbent resin particles, a two-layer structure composed of (A1)-(C) is formed, but composed of (A1)-(C)-(A1). It does not have a sandwich structure. That is, such a two-layer structure is not included in the connecting portion (RC) in the present invention.
Therefore, the structure including the connecting portion (RC) inside the absorbent resin particle means a structure in which this sandwich structure {(A1)-(C)-(A1)} is present inside the absorbent resin particle. means.
The hydrophobic substance (C) is preferably also present on a part of the surface of the absorbent resin particle, more preferably (C) is present on the surface of the absorbent resin particle, C) and (C) inside the absorbent resin particles are continuously connected.
In addition, content of the hydrophobic substance (C) which exists on the surface is measured by the following method. The content of the hydrophobic substance (C) existing inside is obtained by subtracting the content of the surface hydrophobic substance (C) from the content calculated from the total charged quantity of hydrophobic substances.
<Measurement method of content of hydrophobic substance (C)>
In a glass eggplant flask equipped with a cooling tube, 100 parts by weight of absorbent resin particles and an organic solvent (at least 0.01 parts by weight of the hydrophobic substance (D) are dissolved at 25 ° C. to 110 ° C. in 100 parts by weight of the organic solvent). (An organic solvent that can be dissolved is defined as a dissolution temperature.) 300 parts by weight is added and left at the dissolution temperature for 24 hours to obtain an extract of a hydrophobic substance. This extract is filtered using filter paper, collected in a glass eggplant flask weighed in advance, and then weighed after evaporating the solvent with a rotary evaporator. By subtracting the weight of the eggplant flask weighed in advance from the weight after evaporation of the filtrate, the amount of the evaporated and dried product extracted is determined.
Using the sample after extraction remaining on the filter paper, the same operation was repeated twice, and the total amount of the evaporated and dried product obtained by the extraction three times was determined as the content (% by weight) of the hydrophobic substance (C). And

The shape of the connecting portion (RC) is not particularly limited, but from the viewpoint of the anti-absorption property of the absorbent article, a layered shape, a planar shape, a rod shape, a tubular shape, a spherical shape, a mesh shape, and combinations thereof are preferable, and more preferably Layered and spherical, more preferably spherical. The size of the continuous part (RC) (longest part: unit μm) preferably includes 1-1000 linear parts, more preferably 50-800, particularly preferably 100-700, most preferably 200-600. Is included. Within this range, the moisture resistance of the absorbent article is further improved.
The shape and size of the continuous part (RC) are the same as those of the hydrophobic substance (C2) in which the hydrophobic substance (C) contains a hydrocarbon group having a fluorine atom and / or the hydrophobic substance (C3) having a polysiloxane structure. In this case, for example, measurement can be performed by mapping fluorine atoms and / or silicon atoms with an electron beam microanalyzer (EPMA) (for example, JXA-8621MX manufactured by JEOL Ltd.). Further, when the hydrophobic substance (C) is a hydrophobic substance (C1) containing a hydrocarbon group, the absorbent resin particles of the present invention are cut with a microtome and cut with a nonpolar solvent such as hexane and / or dimethyl ether. After washing the cross section, it can be measured by observing with a SEM (scanning electron microscope).

  The structure in which the absorbent resin particles contain part or all of the hydrophobic substance (C) in the interior is obtained by combining the absorbent resin particles with the water content of (1) the hydrophobic substance (C) and the crosslinked polymer (A1). It can be produced by a method of mixing and kneading with a gel, or (2) a method of polymerizing structural units in the presence of the hydrophobic substance (C) to obtain a hydrous gel of the crosslinked polymer (A1).

In the method (1), as the hydrophobic material (C), a material obtained by processing the hydrophobic material (C) into a pulverized product, bead, rod or fiber of a film can be used. The volume average particle size (μm) of the pulverized film is preferably 5 to 50, more preferably 7 to 30, and particularly preferably 10 to 20. The volume average particle diameter (μm) of the beads is preferably 0.5 to 100, more preferably 1 to 30, and particularly preferably 2 to 20. The rod-like length (μm) is preferably 5 to 50, more preferably 7 to 30, particularly preferably 10 to 20, and the diameter (μm) is preferably 0.5 to 50, more preferably 1 to 1. 30, particularly preferably 2-15. The fibrous length (μm) is preferably 5 to 50, more preferably 7 to 30, particularly preferably 10 to 20, and the diameter (μm) is preferably 0.5 to 50, more preferably 1. -30, particularly preferably 2-15. Within these ranges, the moisture resistance of the absorbent article is further improved.

When the hydrophobic substance (C1) containing a hydrocarbon group is used, beads such as Mg stearate beads, polystyrene beads and polyethylene beads, and polyethylene films (for example, Tamapoly, SE625M, UB-1) and polystyrene are used. Examples thereof include pulverized products (volume average particle size 20 to 50 μm) of films such as films (for example, manufactured by Asahi Kasei Corporation: OPS). When using a hydrophobic substance (C3) containing polysiloxane, silicone beads {eg, GE Toshiba Silicones, Inc .: Tospearl 240 (amorphous silicone resin fine powder, volume average particle size 4 μm), Tospearl 3120 (true spherical shape) Silicone resin fine powder, volume average particle size 12 μm), Tospearl 145 (true spherical silicone resin fine powder, volume average particle size 4.5 μm), etc.}. When using a hydrophobic substance (C2) containing a hydrocarbon group having a fluorine atom, a fluorine film {eg, Asahi Glass Co., Ltd .: FLUON PTFE (polytetrafluoroethylene film), FLUON PFA (tetrafluoroethylene and Perfluoroethylene copolymer film), FLUON AFLAS (tetrafluoroethylene and propylene copolymer film), etc.} pulverized product (volume average particle size of 20 to 50 μm).
Of these, beads are preferable from the viewpoint of the anti-moisture property of the absorbent article, and more preferably Mg stearate beads.

As a method for mixing the crosslinked polymer (A1) and the hydrophobic substance (C), the hydrophobic substance (C) is present inside the crosslinked polymer (A1) {ie, the crosslinked polymer (A1) and There is no limitation as long as the hydrophobic substance (C) is mixed so as to have a sandwich structure.
However, the hydrophobic substance (C) is preferably not mixed with the dried polymer of the crosslinked polymer (A1) but with the hydrogel (A1) or the polymerization solution (A1), and more preferably (A1). To be mixed with hydrous gel. In addition, it is preferable to mix uniformly so that mixing may be carried out.
When the crosslinked polymer (A1) is obtained by the aqueous solution polymerization method, the timing for mixing and kneading the hydrophobic substances (C) and (A1) is not particularly limited, but during the polymerization process, immediately after the polymerization process, Examples thereof include crushing (minching) and drying of the hydrogel. Among these, from the viewpoint of the anti-moisture resistance of the absorbent article, it is preferable to be immediately after the polymerization step and during the water-containing gel crushing (mincing) step, and more preferably during the water-containing gel crushing (mincing) step.

  When the crosslinked polymer (A1) is obtained by the reverse phase suspension polymerization method or emulsion polymerization, the timing of mixing the hydrophobic substance (C) and (A1) is not particularly limited, but during the polymerization process {(C) In the presence of (A1)}, immediately after the polymerization step, during the dehydration step (during the step of dehydrating to about 10% by weight of water), immediately after the dehydration step, during the step of separating and distilling off the organic solvent used in the polymerization And during the drying of the hydrogel. Among these, from the viewpoint of the anti-moisture resistance of the absorbent article, it is preferable during the polymerization step, immediately after the polymerization step, during the dehydration step, immediately after the dehydration step, and during the step of separating and distilling off the organic solvent used for the polymerization. Is immediately after the polymerization step during the polymerization step.

  In the case of mixing during the drying of the hydrogel, a normal apparatus such as a bex mill, rubber chopper, pharma mill, mincing machine, impact pulverizer, and roll pulverizer can be used. When mixing in the polymerization solution, a device having a relatively high stirring force such as a homomixer or a biomixer can be used. Moreover, when mixing in drying of a hydrogel, kneading apparatuses, such as SV mixer, can also be used.

  The mixing temperature (° C.) is preferably 20 to 100, more preferably 40 to 90, and particularly preferably 50 to 80. Within this range, it becomes easier to mix evenly and the absorption characteristics are further improved.

  In the method for producing the crosslinked polymer (A1) in the presence of the hydrophobic substance (C), the hydrophobic substance (C) is dissolved or emulsified (dispersed) in the polymer solution of the crosslinked polymer (A1). In addition, the connecting portion can be formed while (C) is precipitated as the polymerization of (A1) proceeds. The polymerization method is the same as in the case of the crosslinked polymer (A1), except that the polymerization is performed in the presence of the hydrophobic substance (C).

The hydrophobic substance (C) can also be used in a form dissolved and / or emulsified in water and / or a volatile solvent (however, no emulsifier is used). The volatile solvent preferably has a vapor pressure (Pa) at 20 ° C. of 0.13 to 5.3, more preferably 0.15 to 4.5, particularly preferably, from the viewpoint of easy removal. Is from 0.23 to 3.8.
Examples of the volatile solvent include alcohols having 1 to 3 carbon atoms (such as methanol, ethanol and isopropyl alcohol), hydrocarbons having 5 to 8 carbon atoms (such as pentane, hexane, cyclohexane and toluene), and ethers having 2 to 4 carbon atoms ( Dimethyl ether, diethyl ether, tetrahydrofuran, etc.), C3-C4 ketones (acetone, methyl ethyl ketone, etc.), C3-C5 esters (ethyl formate, ethyl acetate, isopropyl acetate, diethyl carbonate, etc.) and the like. When water and / or a volatile solvent is used, the amount (% by weight) of these used is preferably 1 to 900, more preferably 5 to 700, particularly preferably based on the weight of the hydrophobic substance (C). 10-400. When water and a volatile solvent are used, the amount (% by weight) of water used is preferably from 50 to 98, more preferably from 60 to 95, particularly preferably from 70 to 90, based on the weight of water and the volatile solvent. It is.

From the viewpoint of the anti-fogging property of the absorbent article, the structure in which the absorbent resin particles contain a part or all of the hydrophobic substance (C) therein includes hydrophilic material particles (d1) or hydrophobic material particles. It is preferable to have a structure in which the material particles (D) in which a part or all of the surface of (d2) is coated or impregnated with the hydrophobic substance (C) are contained inside the absorbent resin particles.
As the material particles (D), those obtained by coating or impregnating the hydrophobic material (C) with the hydrophilic material particles (d1) or the hydrophobic material particles (d2) can be used.

Examples of the hydrophilic material particles (d1) include hydrophilic organic polymer particles (d11) and hydrophilic inorganic particles (d12).
Examples of the hydrophilic organic polymer particles (d11) include particles of polymer electrolyte {cross-linked polymer (A2), etc.], cellulose (pulp, cotton, sawdust, straw, etc.), wool, microfibril, and bacterial cellulose.
In addition, a crosslinked polymer (A2) is a crosslinked polymer which has a water-soluble vinyl monomer (a1) and / or a hydrolyzable vinyl monomer (a2), and a crosslinking agent (b) as an essential structural unit. Here, the crosslinked polymer having the water-soluble vinyl monomer (a1) and / or the hydrolyzable vinyl monomer (a2) and the crosslinking agent (b) as essential constituent units is the same as the above-mentioned crosslinked polymer (A1). The preferred ones are also the same.

  Examples of the hydrophilic inorganic particles (d12) include particles such as glass, silica gel, silica, and clay.

The hydrophobic material particles (d2) include hydrophobic organic polymer particles (d21) and hydrophobic inorganic particles (d22).
As the hydrophobic organic polymer particles (d21), particles such as synthetic resin having a weight average molecular weight of 1,000 to 1,000,000 can be used, and a hydrophobic substance (C1) that can be used for the connecting portion (RC), polystyrene, Particles such as resin, polyethylene resin, polypropylene resin, acrylic resin, polyester resin, polyamide resin, epoxy resin, and urethane resin are used.
Examples of the polystyrene resin include polystyrene, styrene-ethylene copolymer, styrene-butadiene copolymer and the like.
Examples of the polyethylene resin include high-density polyethylene and low-density polyethylene.
Examples of the polypropylene resin include polypropylene and ethylene-propylene copolymer.
Examples of the acrylic resin include polymers such as methyl (meth) acrylate, ethyl (meth) acrylate, and (meth) acrylic ester of a long-chain alkyl alcohol having 8 to 22 carbon atoms.
Examples of the polyester resin include polyethylene terephthalate and polybutadiene terephthalate.
Examples of the polyamide resin include nylon.
Examples of the epoxy resin include a cured product of a normal epoxy resin.
Examples of the urethane resin include a cured product of a normal polyol isocyanate.

  Examples of the hydrophobic inorganic particles (d22) include particles of carbon fiber, kaolin, talc, mica, bentonite, sericite, asbestos, shirasu, and the like.

  Of these, the hydrophilic material particles (d1) are preferred, the hydrophilic organic polymer particles (d11) are more preferred, the cellulose and polyelectrolyte particles are more preferred, and the crosslinked polymer (A2) is particularly preferred. Most preferred are polyacrylic acid (sodium salt) crosslinked particles.

  The shape of the hydrophilic material particles (d1) and the hydrophobic material particles (d2) may be any of an irregular shape (crushed shape), a true spherical shape, a film shape, a rod shape, and a fiber shape, but the irregular shape (crushed shape). Alternatively, a true spherical shape is preferable, and a true spherical shape is more preferable.

The volume average particle diameter (μm) of the hydrophilic material particles (d1) and the hydrophobic material particles (d2) is preferably 1 to 30, more preferably 1.5 to 25, particularly preferably 2 to 20, and more particularly preferably. Is 2.5-15, most preferably 3-10. Within this range, the moisture resistance of the absorbent article is further improved.
The volume average particle diameter is measured by a light scattering method (solvent: cyclohexane or the like) in accordance with JIS Z8825-1: 2001.

When the material particle (D) is a material in which the hydrophobic material particle (d2) is coated or impregnated with the hydrophobic substance (C), the hydrophobic substance (C) to be coated or impregnated includes the resistance of the absorbent article. Of the hydrophobic substances (C1) containing a hydrocarbon group, from the viewpoint of moletability and the like, polyolefin resins, waxes and long-chain fatty acid esters are preferable, more preferably waxes and long-chain fatty acid esters, particularly preferably waxes, most preferably Paraffin wax is preferred. Similarly, among the hydrophobic substances (C2) containing a hydrocarbon group having a fluorine atom, perfluoroalkanes and perfluoroalkyl ethers are preferable, perfluoroalkyl ethers are more preferable, and dipentafluoropropyl is particularly preferable. Ether, diheptafluoropropyl ether, diheptafluorobutyl ether and dinonafluorohexyl ether, most preferably diheptafluoropropyl ether and diheptafluorobutyl ether. Similarly, among the hydrophobic substance (C3) having a polysiloxane structure, polydimethylsiloxane and alkoxy-modified polysiloxane are preferable, and polydimethylsiloxane is more preferable.
Of these hydrophobic substances, the hydrophobic substance (C3) having a polysiloxane structure is preferable from the viewpoint of anti-fogging property of the absorbent article.

When the material particle (D) is a material in which the hydrophilic material particle (d1) is coated or impregnated with the hydrophobic substance (C), the hydrophobic substance (C) to be coated or impregnated includes the resistance of the absorbent article. Of the hydrophobic substance (C1) containing a hydrocarbon group, from the viewpoint of molecularity and the like, polyolefin resin derivatives, wax derivatives and long-chain fatty acid esters are preferable, more preferably wax derivatives and long-chain fatty acid esters, and particularly preferably. Long chain fatty acid esters, most preferably sucrose stearate monoester and sucrose stearate diester. Similarly, among the hydrophobic substance (C2) containing a hydrocarbon group having a fluorine atom, perfluoroalkyl carboxylic acid and perfluoroalkyl alcohol are preferable, and more preferably perfluoroalkyl carboxylic acid metal salt and perfluoroalkyl. Alkyl alcohol, particularly preferably a perfluoroalkylcarboxylic acid metal salt. Similarly, among the hydrophobic substances (C3) having a polysiloxane structure, polyether-modified polysiloxane, carboxyl-modified polysiloxane, epoxy-modified polysiloxane and amino-modified polysiloxane are preferable, and carboxyl-modified polysiloxane is more preferable. Epoxy-modified polysiloxanes and amino-modified polysiloxanes, particularly preferably carboxyl-modified polysiloxanes and amino-modified polysiloxanes, most preferably amino-modified polysiloxanes.
Among these hydrophobic substances, the hydrophobic substance (C2) which is a long-chain fatty acid ester is preferable from the viewpoint of absorption characteristics, particularly preferably sucrose stearate, most preferably sucrose stearate monoester and sucrose. It is a sugar stearic acid diester.

  The volume average particle diameter (μm) of the material particles (D) is preferably 1 to 30, more preferably 1.5 to 25, particularly preferably 2 to 20, more particularly preferably 2.5 to 15, most preferably. 3-10. Within this range, the anti-fogging property of the absorbent article is further improved. The volume average particle diameter is measured in the same manner as the hydrophilic material particles (d1) and the hydrophobic material particles (d2).

  The content (% by weight) of the hydrophobic substance (C) in the material particles (D) is preferably 0.001 to 10, more preferably 0.005 to 8, particularly preferably based on the weight of (D). Is 0.07-7, most preferably 0.1-6. Within this range, the moisture resistance of the absorbent article is further improved.

  The content (% by weight) of the material particles (D) is preferably 0.01 to 20, more preferably 0.05 to 10, and most preferably 0.1 based on the weight of the crosslinked polymer (A1). To 1.0, particularly preferably 0.2 to 0.9, and most preferably 0.3 to 0.8. Within this range, the anti-fogging property of the absorbent article is further improved.

  When the absorbent resin particles have a structure comprising the material particles (D), the absorbent resin particles are (1) a method of mixing and kneading the material particles (D) and the hydrogel of the crosslinked polymer (A1). Or (2) It can be produced by a method of polymerizing in the presence of the material particles (D) to obtain a hydrogel of the crosslinked polymer (A1).

(1) As a method of mixing and kneading the water-containing gel of the crosslinked polymer (A1) and the material particles (D), the material particles (D) are present inside the water-containing gel of the crosslinked polymer (A1) { There is no limitation as long as the crosslinked polymer (A1) and the material particles (D) are mixed and kneaded so as to have a sandwich structure.
However, the material particles (D) are preferably mixed and kneaded with the hydrated gel of (A1) or the polymerization solution of (A1), not the dried product of the crosslinked polymer (A1), more preferably (A1). It is mixed and kneaded with the hydrous gel. In addition, it is preferable to mix and knead | mix uniformly so that it may knead.
Although there is no restriction | limiting in particular as a timing which mixes material particle | grains (D) and (A1), It is the same as the case where the hydrophobic substance (C) mentioned above is mixed. As the mixing / kneading apparatus, the same apparatus as used for mixing the hydrophobic substance (C) can be used.

(2) In the method of obtaining a crosslinked polymer (A1) by polymerizing in the presence of the material particles (D), the material particles (D) are emulsified or dispersed in the polymer solution of the crosslinked polymer (A1), and polymerization is performed. This is the same as the case of polymerizing the crosslinked polymer (A1) in the presence of the hydrophobic substance (C).

  When the hydrophobic material (C) is coated or impregnated on part or all of the surface of the hydrophilic material particles (d1) or the hydrophobic material particles (d2), the hydrophobic material (C) is dissolved or emulsified in a solvent. It can be used as a liquid by dispersing or heating to a melting point or higher of (C).

  In order to coat or impregnate the hydrophobic material (C) on the hydrophilic material particles (d1) or the hydrophobic material particles (d2), the liquid is sprayed on (d1) or (d2), or (d1 ) Or (d2) can be achieved by dipping. The hydrophilic dispersion particles (d1) or the hydrophobic material particles (d2) are brought into contact with the emulsified dispersion of the solid hydrophobic substance (C) or (C), and then heated to the melting point of (C) or higher. It can also be coated or impregnated.

When a solvent is used for coating or impregnation, it is preferable to distill off the solvent. In this case, the content (% by weight) of the organic solvent after the distillation is preferably 0 to 10, more preferably 0 to 5, particularly preferably 0 to 3 based on the weight of the material particles (D). Most preferably, it is 0-1. Within this range, the moisture resistance (particularly the amount of water retained) of the absorbent article is further improved. Moreover, when water is contained in the solvent, the water content (% by weight) after distillation is preferably 0 to 20, more preferably 0 to 10, particularly preferably 0 to 5, based on the weight of the material particles (D). Most preferably, it is 0-2. Within this range, the moisture resistance (particularly the amount of water retained) of the absorbent article is further improved.
The method for distilling off and the method for measuring the content of the solvent are the same as those for the crosslinked polymer (A1).

The solvent that can be used is not particularly limited as long as it dissolves (C), but the above-mentioned water and / or volatile solvent are preferable.
Examples of a mixing device that can be applied to spraying, dipping, or contact include a nauter mixer and a turbulizer.

The water-containing gel containing the hydrophobic substance (C) can be chopped as necessary. The size (longest diameter) of the hydrogel particles after chopping is preferably 50 μm to 10 cm, more preferably 100 μm to 2 cm, and particularly preferably 1 mm to 1 cm. Within this range, the drying property in the drying process is further improved.
As the shredding method, the same method as in the case of the crosslinked polymer (A1) can be adopted.

When a solvent (including an organic solvent and / or water) is used for production of the absorbent resin particles, the solvent can be distilled off after polymerization.
When the solvent contains an organic solvent, the content (% by weight) of the organic solvent after the distillation is preferably 0 to 10, more preferably 0 to 5, particularly preferably 0, based on the weight of the absorbent resin particles. ~ 3, most preferably 0-1. It is. Within this range, the absorption performance (particularly the water retention amount) of the absorbent resin particles is further improved.

Moreover, when water is contained in the solvent, the water content (% by weight) after the distillation is preferably 0 to 20, more preferably 1 to 10, particularly preferably 2 to 9, based on the weight of the absorbent resin particles. Most preferably, it is 3-8. Within this range, the absorption performance (particularly the water retention amount) and the breakability of the absorbent resin particles after drying are further improved.
In addition, the content of the organic solvent, the method for measuring the water content, and the method for distilling off the solvent are the same as in the case of the crosslinked polymer (A1).

The absorbent resin particles can be pulverized. When the absorbent resin particles contain a solvent, the solvent is preferably pulverized after being distilled off (dried).
When pulverizing, the weight average particle size (μm) after pulverization is preferably 400 to 650, particularly preferably 450 to 600, and most preferably 500 to 540. Within this range, handling properties after pulverization (powder fluidity of absorbent resin particles and the like) and anti-fogging properties of the absorbent article are further improved. In addition, a weight average particle diameter can be measured like the case of a crosslinked polymer (A1).

The smaller the content of fine particles, the better the absorption performance. The content of fine particles of 106 μm or less in the total particles is preferably 3% by weight or less, and more preferably the content of fine particles of 150 μm or less in the total particles is 3% by weight. It is as follows. The content of the fine particles can be determined using a plot created when determining the above weight average particle diameter.
For pulverization and particle size adjustment, the same method as in the case of the crosslinked polymer (A1) can be employed.

  The apparent density (g / ml) of the absorbent resin particles of the present invention is preferably 0.56 to 0.62, more preferably 0.57 to 0.61, and particularly preferably 0.58 to 0.60. . Within this range, the anti-fogging property of the absorbent article is further improved. The apparent density can be measured in the same manner as in the case of the crosslinked polymer (A1).

  The shape of the absorbent resin particles is not particularly limited, and examples thereof include an irregularly crushed shape, a flake shape, a pearl shape, and a rice grain shape. Among these, from the viewpoint of good entanglement with the fibrous material in the use of paper diapers and the like and no fear of dropping off from the fibrous material, an irregular crushed shape is preferable.

  The absorbent resin particles can be subjected to surface crosslinking as necessary. As the crosslinking agent (surface crosslinking agent) for performing the surface crosslinking, the same as the internal crosslinking agent (b) can be used. As the surface cross-linking agent, from the viewpoint of the absorption performance of the absorbent resin particles, the water-soluble substituent of the water-soluble vinyl monomer (a1) and / or the water-soluble substituent generated by hydrolysis of the vinyl monomer (a2) is reacted. The cross-linking agent (b3) having at least two functional groups that can be used is preferable, more preferably polyvalent glycidyl, particularly preferably ethylene glycol diglycidyl ether and glycerin diglycidyl ether, and most preferably ethylene glycol diglycidyl ether.

  In the case of surface cross-linking, the content (% by weight) of the surface cross-linking agent is the total weight of the vinyl monomers (a1) and / or (a2), the internal cross-linking agent (b) and other vinyl monomers (a3) used as necessary. Is preferably 0.001 to 7, more preferably 0.002 to 5, particularly preferably 0.003 to 4. That is, in this case, the upper limit of the content (% by weight) of the surface cross-linking agent is preferably 7 based on the total weight of (a1) and / or (a2), (b) and (a3), more preferably 5, particularly preferably 4. Similarly, the lower limit is preferably 0.001, more preferably 0.002, and particularly preferably 0.003. In this range, the absorption performance is further improved. Surface cross-linking can be achieved by a method of spraying or impregnating absorbent particles with an aqueous solution containing a surface cross-linking agent, followed by heat treatment (100 to 200 ° C.).

  The absorbent resin particles of the present invention may contain other additives (for example, known preservatives, fungicides, antibacterial agents, antioxidants, ultraviolet rays (for example, JP 2003-225565 A, JP 2006-131767 A). Absorbers, colorants, fragrances, deodorants, inorganic powders, organic fibrous materials, etc.}. When these additives are contained, the content (% by weight) of the additives is preferably 0.001 to 10, more preferably 0.01 to 5, particularly preferably based on the weight of the crosslinked polymer (A1). Preferably it is 0.05 to 1, most preferably 0.1 to 0.5.

  The absorption amount (M) (ml / g) of the absorbent resin particles of the present invention by the DW method is preferably from 14 to 19 in terms of the absorption amount (M1) after 1 minute from the viewpoint of the resistance to moisture of the absorbent article. More preferably, it is 15-18, Most preferably, it is 16-17. The absorption amount (M2) after 2 minutes is preferably 26 to 33, more preferably 27 to 32, and particularly preferably 28 to 31. The absorption amount (M3) after 5 minutes is preferably 42 to 50, more preferably 43 to 49, and particularly preferably 44 to 48. The absorption amount (M4) after 10 minutes is preferably 52 to 59, more preferably 53 to 58, and particularly preferably 54 to 57. Within this range, the anti-fogging property of the absorbent article is further improved. The amount absorbed by the DW method includes the content of the hydrophobic substance (C), the apparent density of the absorbent resin particles, the weight average particle diameter of the absorbent resin particles, the volume average particle diameter and the content of the material particles (D), etc. By adjusting to the said preferable range, the absorption amount by DW method can be adjusted to a preferable range. Moreover, as a manufacturing method of an absorbent resin particle, the manufacturing method which mixes and knead | mixes the water-containing gel of a crosslinked polymer (A1) and material particle | grains (D) is preferable from a viewpoint which can adjust DW to a preferable range.

  The DW (Demand Wettability) method is a measurement method performed using the apparatus shown in FIG. 1 in a room at 25 ° C. and a humidity of 50%. The measuring apparatus shown in FIG. 1 includes a burette part (2) {scale capacity 50 ml, length 86 cm, inner diameter 1.05 cm,}, conduit {inner diameter 7 mm}, and measuring table (6). The burette part (2) is connected to the rubber stopper (1) at the upper part, the intake introduction pipe (9) {tip inner diameter 3 mm} and the cock (7) at the lower part, and the upper part of the intake introduction pipe (9) is There is a cock (8). A conduit is attached from the burette part (2) to the measurement table (6). At the center of the measurement table (6), there is a hole with a diameter of 3 mm as a physiological saline supply unit, and a conduit is connected.

  Using the measuring device of this configuration, first, the cock (7) of the burette part (2) and the cock (8) of the air introduction pipe (9) are closed, and a predetermined amount of physiological saline (salt) adjusted to 25 ° C. (Concentration 0.9 wt%) from the top of the burette part (2), and after plugging the top of the buret with the rubber plug (1), the cock (7) of the burette part (2) and the cock of the air introduction pipe (9) Open (8). Next, after wiping off the physiological saline overflowing the measurement table (6), the upper surface of the measurement table (6) and the surface of the saline solution coming out from the conduit port at the center of the measurement table (6) The height of the measurement table (6) is adjusted so that it is the same height. While wiping the physiological saline from the physiological saline supply part, the surface of the physiological saline in the burette part (2) is adjusted to the top (0 ml line) of the burette part (2) scale.

  Subsequently, the cock (7) of the burette part (2) and the cock (8) of the air introduction pipe (9) are closed, and the plain weave nylon mesh (on the measurement table (6) is placed so that the physiological saline supply part is at the center. 5) (Opening 63 μm, 5 cm × 5 cm) is placed on this plain weave nylon mesh (5), and 0.50 g in a range of 2.7 cm in diameter with the physiological saline supply part of the measuring table (6) as the center. The absorbent resin particles (4) are uniformly dispersed. Thereafter, the cock (7) of the burette part (2) and the cock (8) of the air introduction pipe (9) are opened.

  When the absorbent resin particles (4) begin to absorb water and the first foam introduced from the air introduction tube (9) reaches the surface of the physiological saline in the burette portion (2) (burette portion (2) The measurement start time is defined as the time when the physiological saline water in the inside drops, and the amount of physiological saline (3) in the burette portion (2) is continuously reduced (the physiological state in which the absorbent resin particles (4) have absorbed water). Saline amount) M (ml) is read. The absorption amount of the absorbent resin particles (4) after the elapse of a predetermined time from the start of water absorption is determined by the following equation.

  Absorption by DW method (ml / g) = M ÷ 0.50

  The water retention amount (g / g) of the absorbent resin particles of the present invention is preferably from 28 to 45, more preferably from 32 to 40, particularly preferably from 34 to 38, from the viewpoint of anti-fogging properties of the absorbent article. The water retention amount of the absorbent resin particles is measured by the following method.

<Measurement method of water retention amount of absorbent resin particles>
1.00 g of a measurement sample is put into a tea bag (20 cm long, 10 cm wide) made of a nylon net having a mesh size of 63 μm (JIS Z8801-1: 2006), and 1,000 ml of physiological saline (saline concentration 0.9% by weight). After being immersed in the inside for 1 hour without stirring, it was suspended for 15 minutes and drained. Thereafter, each tea bag is placed in a centrifuge, centrifuged at 150 G for 90 seconds to remove excess physiological saline, and the weight (h1) including the tea bag is measured to obtain the water retention amount from the following equation. In addition, the temperature of the used physiological saline and measurement atmosphere shall be 25 degreeC +/- 2 degreeC.
The weight of the tea bag after centrifugal dehydration is measured (h2) in the same manner as above except that no measurement sample is used.

Water retention amount (g / g) = (h1)-(h2)

  The absorption amount under load (g / g) of the absorbent resin particles of the present invention is preferably 15 to 27, more preferably 17 to 25, and particularly preferably 19 to 23 from the viewpoint of anti-fogging property of the absorbent article. is there.

The absorption amount under load is measured as follows.
<Measurement method of absorption amount of absorbent resin particles under load>
0.16 g of a measurement sample sieved to a particle diameter of 250 to 500 μm in a cylindrical plastic tube (inner diameter: 25 mm, height: 34 mm) having a nylon mesh of 63 μm (JIS Z8801-1: 2006) pasted on the bottom. Were weighed and the cylindrical plastic tube was placed vertically so that the measurement sample had a substantially uniform thickness on the nylon mesh, and then a weight (weight: 310.6 g, outer diameter: 24. 5mm,). After measuring the weight (W1) of the entire cylindrical plastic tube, a cylindrical type containing a measurement sample and a weight in a petri dish (diameter: 12 cm) containing 60 ml of physiological saline (salt concentration 0.9% by weight). Stand the plastic tube vertically and immerse it with the nylon mesh side down, and let stand for 60 minutes. After 60 minutes, pull up the cylindrical plastic tube from the petri dish, tilt it diagonally, remove the dripping water droplets, weigh the entire cylindrical plastic tube containing the measurement sample and weight (W2), Obtain the amount absorbed under load. In addition, the temperature of the physiological saline used and measurement atmosphere is 25 degreeC +/- 2 degreeC.

Absorption under load (g / g) = {(W2)-(W1)} / 0.16

  The absorbent resin particles of the present invention can be used as an absorbent body together with a fibrous material. The structure and manufacturing method of the absorber are the same as those known in the art (Japanese Patent Laid-Open Nos. 2003-225565, 2006-131767, and 2005-097569, etc.). Moreover, it is preferable that this absorber comprises absorbent articles {paper diapers, sanitary napkins, etc.}. The manufacturing method and the like of the absorbent article are the same as known ones (Japanese Unexamined Patent Publication Nos. 2003-225565, 2006-131767, and 2005-097569, etc.).

  When the absorbent resin particle of the present invention is used as an absorbent body together with a fibrous material, the weight ratio of the absorbent resin particle to the fiber (weight of absorbent resin particle / weight of fiber) is preferably 40/60 to 95/5. More preferably, it is 70/30 to 90/10, and particularly preferably 75/25 to 85/15.

  Hereinafter, although an example and a comparative example explain the present invention further, the present invention is not limited to these. Unless otherwise specified, “part” means “part by weight” and “%” means “% by weight”. The absorption amount by the DW method, the water retention amount of the absorbent resin particles, and the absorption amount under load of the absorbent resin particles were measured by the methods described above.

<Production Example 1>
Water-soluble vinyl monomer (a1-1) {acrylic acid, manufactured by Mitsubishi Chemical Corporation, purity 100%} 155 parts (2.15 mole parts), crosslinking agent (b1) {pentaerythritol triallyl ether, manufactured by Daiso Corporation } 0.6225 parts (0.0024 mole part) and 340.27 parts deionized water were kept at 3 ° C. with stirring and mixing. Nitrogen was introduced into the mixture to bring the dissolved oxygen amount to 1 ppm or less, and then 0.62 part of 1% aqueous hydrogen peroxide solution, 1.1625 part of 2% aqueous ascorbic acid solution and 2% 2,2′-azobis [ 2.325 parts of an aqueous solution of 2-methyl-N- (2-hydroxyethyl) -propionamide] was added and mixed to initiate polymerization. After the temperature of the mixture reached 90 ° C., polymerization was carried out at 90 ± 2 ° C. for about 5 hours to obtain a hydrogel (1).

  Next, 400 parts of this hydrogel (1) was shredded with a mincing machine (12 VR-400K manufactured by ROYAL), and 102.27 parts of 48.5% sodium hydroxide aqueous solution was added, mixed and neutralized. A cut gel (1) was obtained. Further, the chopped gel (1) was dried with a ventilation type band dryer {140 ° C., wind speed 2 m / sec} to obtain a dried product. The dried product is pulverized with a juicer mixer (Osterizer BLENDER manufactured by Oster Co., Ltd.) and then adjusted to a particle size of 25 to 45 μm using a sieve having an opening of 25 and 45 μm to obtain hydrophilic material particles (d1-1). It was. The volume average particle diameter of the hydrophilic material particles (d1-1) was 30 μm.

<Production Example 2>
Liquid obtained by dispersing 0.5 part of hydrophobic substance (C-1) {amino-modified silicone (Shin-Etsu Chemical Co., Ltd. product: KF880)} in 50 parts of methanol in 50 parts of hydrophilic material particles (d1-1) After adding 5 parts and stirring at 25 ° C. for 5 minutes, it was evaporated to dryness at 80 ° C. for 2 hours to obtain material particles (D-1).

<Production Example 3>
The hydrophilic material particles (d1-2) were prepared in the same manner as in Production Example 1 except that the sieves having openings of 25 and 45 μm were changed to “screens of openings of 15 and 25 μm” and adjusted to a particle size of 15 to 25 μm. ) The volume average particle diameter of the hydrophilic material particles (d1-2) was 20 μm.

<Production Example 4>
Hydrophobic material particles (d1-2) with 50 parts of hydrophobic substance (C-2) {sucrose stearate (Mitsubishi Chemical Foods, Ryoto Sugar Ester S-570 / S-770 weight ratio = 50 / 50 mixture)} 52.5 parts of a solution in which 2.5 parts are dissolved in 50 parts of cyclohexane are added and stirred at 25 ° C. for 5 minutes, and then evaporated to dryness at 80 ° C. for 2 hours. 2) was obtained.

<Production Example 5>
62.89 parts of acrylic acid was diluted with 37.02 parts of water and neutralized by adding 71.88 parts of 35% aqueous sodium hydroxide while cooling to 20-15 ° C. To this solution, 0.252 part of ethylene glycol diglycidyl ether, 0.018 part of sodium hypophosphite monohydrate and 0.192 part of potassium persulfate were added and dissolved, and stirred at 25 ° C. to obtain an aqueous monomer solution ( 1) was obtained. Next, after dissolving 1.6 parts of the hydrophobic substance (C-2) in 312 parts of cyclohexane while heating to 60 ° C., the monomer aqueous solution (1) was added, and the biomixer (Nippon Seiki Co., Ltd.) was added at 25 ° C. The mixture was stirred and dispersed at 10,000 rpm for 5 minutes using ABM-2 manufactured by the company, deoxygenated by flowing nitrogen, and dispersion (1) was obtained.

  Next, 312 parts of cyclohexane is placed in a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer and a nitrogen gas introduction tube, and 1.6 parts of a hydrophobic substance (C-2) is added thereto, followed by stirring. While replacing with nitrogen, the mixture was heated to 70 ° C. and dissolved. And the dispersion liquid was dripped for 60 minutes at 8.23 parts / min, keeping at 70 degreeC. Thereafter, after aging at 75 ° C. for 30 minutes, the water content of the resin is about 10% by azeotroping water with cyclohexane (infrared moisture meter: FD-100 type, manufactured by Kett, measured at 180 ° C. for 20 minutes). Removed until Thereafter, cyclohexane was removed by evaporation to obtain material particles (D-3). The volume average particle diameter of the material particles (D-3) was 3 μm.

<Production Example 6>
In the same manner as in Production Example 5, except that 1.6 parts of “hydrophobic substance (C-2)” is changed to “2.4 parts of hydrophobic substance (C-2)”, the material particles (D-4) Got. The volume average particle diameter of the material particles (D-4) was 1 μm.

<Production Example 7>
In a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, and a nitrogen gas introduction tube, a cyclohexane part is placed, and after 3.2 parts of a hydrophobic substance (C-2) is added thereto, nitrogen is added while stirring. The temperature was raised to 70 ° C. and dissolved. And after cooling to 25 degreeC, the monomer aqueous solution (1) obtained by manufacture example 5 was added, nitrogen substitution was carried out, stirring, and it heated up to 70 degreeC as it was, and started polymerization. Thereafter, after aging at 75 ° C. for 30 minutes, the water content of the resin is about 10% by azeotroping water with cyclohexane (infrared moisture meter: FD-100 type, manufactured by Kett, measured at 180 ° C. for 20 minutes). Removed until Thereafter, cyclohexane was removed by evaporation to obtain material particles (D-5). The volume average particle diameter of the material particles (D-5) was 10 μm.

<Production Example 8>
62.89 parts of acrylic acid was diluted with 37.02 parts of water and neutralized by adding 71.88 parts of 35% aqueous sodium hydroxide while cooling to 20-15 ° C. To this solution, 0.252 parts of ethylene glycol diglycidyl ether, 0.018 part of sodium hypophosphite monohydrate and 0.031 part of potassium persulfate were added and dissolved, and nitrogen was added while stirring at 25 ° C. It flowed in and deoxygenated, and monomer aqueous solution (2) was obtained. Next, 4.0 parts of a hydrophobic substance (C-2) was dissolved in 304 parts of cyclohexane while heating to 60 ° C., and nitrogen was introduced to perform deoxygenation to obtain a cyclohexane solution (1).

  Next, 312 parts of cyclohexane is placed in a reaction vessel equipped with a stirrer, a reflux condenser, a thermometer, and a nitrogen gas introduction pipe, and 0.8 part of a hydrophobic substance (C-2) is added thereto, followed by stirring. While replacing with nitrogen, the mixture was heated to 70 ° C. and dissolved. Then, the monomer aqueous solution (2) and the cyclohexane solution (1) were simultaneously added dropwise while maintaining the temperature at 70 ° C., the monomer aqueous solution (2) was added at 2.91 parts / min for 60 minutes, and the cyclohexane solution (1) was added at 4. The polymerization was carried out dropwise at 4 parts / min for 70 minutes. Thereafter, after aging at 75 ° C. for 30 minutes, the water content of the resin is about 10% by azeotroping water with cyclohexane (infrared moisture meter: FD-100 type, manufactured by Kett, measured at 180 ° C. for 20 minutes). Removed until Thereafter, cyclohexane was removed by evaporation to obtain material particles (D-6). The volume average particle diameter of the material particles (D-6) was 25 μm.

<Example 1>
0.454 parts of material particles (D-1) obtained in Production Example 2 while chopping 502.27 parts of the chopped gel (1) obtained in Production Example 1 with a mincing machine (12VR-400K manufactured by ROYAL) Were added and mixed to obtain a chopped gel (2). Further, the chopped gel (2) was dried with a ventilation band dryer {150 ° C., wind speed 2 m / sec} to obtain a dried product. The dried product was pulverized with a juicer mixer (Osterizer BLENDER manufactured by Oster Co., Ltd.) and then adjusted to a particle size of 150 to 850 μm using a sieve having an opening of 150 and 850 μm to obtain dried particles. While stirring 100 parts of the dry particles (high-speed stirring turbulizer manufactured by Hosokawa Micron: rotation speed 2000 rpm), a 2% water / methanol mixed solution of ethylene glycol diglycidyl ether (water / methanol weight ratio = 70/30). 5 parts were added while being sprayed and mixed, and the mixture was allowed to stand at 150 ° C. for 30 minutes to crosslink the surface to obtain the absorbent resin particles (1) of the present invention. The weight average particle diameter of the absorbent resin particles (1) was 500 μm, and the apparent density was 0.61 g / ml. Further, 0.0002% of the hydrophobic substance (C) was present inside the water absorbent resin particles (1), and 0.0001% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (2).

<Example 2>
“0.454 parts of material particles (D-1) obtained in Production Example 2” were changed to “0.756 parts of material particles (D-2) obtained in Production Example 4”; The absorbent resin particles (2) of the present invention were obtained in the same manner as in Example 1, except that the "850 μm sieve" was changed to "the sieve having 125 and 710 µm openings" and adjusted to a particle size of 125 to 710 µm. . The weight average particle diameter of the absorbent resin particles (2) was 400 μm, and the apparent density was 0.59 g / ml. Further, 0.022% of the hydrophobic substance (C) was present inside the water absorbent resin particles (2), and 0.003% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (2).

<Example 3>
“0.454 parts of the material particles (D-1) obtained in Production Example 2” were changed to “1.513 parts of the material particles (D-3) obtained in Production Example 5”; Absorbent resin particles (3) of the present invention were obtained in the same manner as in Example 1, except that the "850 μm sieve" was changed to "a sieve having an opening of 425 and 850 µm" and adjusted to a particle size of 425 to 850 µm. . The weight average particle diameter of the absorbent resin particles (3) was 650 μm, and the apparent density was 0.57 g / ml. Further, 0.037% of the hydrophobic substance (C) was present inside the water absorbent resin particles (3), and 0.004% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (3).

<Example 4>
“0.454 parts of the material particles (D-1) obtained in Production Example 2” were changed to “1.21 parts of the material particles (D-4) obtained in Production Example 6”, and “150 openings and Absorbent resin particles (4) of the present invention were obtained in the same manner as in Example 1, except that “850 μm sieve” was changed to “screens of 355 and 850 μm openings” and adjusted to a particle size of 355 to 850 μm. . The weight average particle diameter of the absorbent resin particles (4) was 600 μm, and the apparent density was 0.58 g / ml. Further, 0.045% of the hydrophobic substance (C) was present inside the water-absorbent resin particles (4), and 0.003% of the hydrophobic substance (C) was present on the surface of the water-absorbent resin particles (4).

<Example 5>
“0.454 part of the material particle (D-1) obtained in Production Example 2” was changed to “0.151 part of the material particle (D-5) obtained in Production Example 7”, and “150 openings and Absorbent resin particles (5) of the present invention were obtained in the same manner as in Example 1, except that “850 μm sieve” was changed to “125 and 710 μm sieve” and adjusted to a particle size of 125 to 710 μm. . The weight average particle diameter of the absorbent resin particles (5) was 400 μm, and the apparent density was 0.62 g / ml. Further, 0.004% of the hydrophobic substance (C) was present inside the water absorbent resin particles (5), and 0.001% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (5).

<Example 6>
“0.454 parts of the material particles (D-1) obtained in Production Example 2” were changed to “0.454 parts of the material particles (D-6) obtained in Production Example 8”, and “150 openings and Absorbent resin particles (6) of the present invention were obtained in the same manner as in Example 1, except that “850 μm sieve” was changed to “mesh 250 and 850 μm sieve” to adjust the particle size to 250 to 850 μm. . The weight average particle diameter of the absorbent resin particles (6) was 540 μm, and the apparent density was 0.60 g / ml. Further, 0.015% of the hydrophobic substance (C) was present inside the water-absorbent resin particles (6), and 0.003% of the hydrophobic substance (C) was present on the surface of the water-absorbent resin particles (6).

<Example 7>
“0.454 parts of the material particles (D-1) obtained in Production Example 2” were added to 0.212 parts of a hydrophobic substance (C-3) {stearyl alcohol} and a hydrophobic substance (C-4) {Mg stearate , Volume average particle size 8 μm} 0.378 parts ”, and“ sieve 150 and 850 μm sieve ”changed to“ 150 and 710 μm sieve ”and adjusted to a particle size of 150 to 710 μm Otherwise, the absorbent resin particles (7) of the present invention were obtained in the same manner as in Example 1. The weight average particle diameter of the absorbent resin particles (7) was 450 μm, and the apparent density was 0.58 g / ml. Further, 0.381% of the hydrophobic substance (C) was present inside the water absorbent resin particles (7), and 0.009% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (7).

<Example 8>
“0.454 part of the material particle (D-1) obtained in Production Example 2” was changed to “0.124 part of a hydrophobic substance (C-3) {stearyl alcohol}”, and “aperture 150 and 850 μm” Absorbent resin particles (8) of the present invention were obtained in the same manner as in Example 1 except that the sieve was changed to “a sieve having an opening of 250 and 850 μm” and adjusted to a particle size of 250 to 850 μm. The weight average particle diameter of the absorbent resin particles (8) was 540 μm, and the apparent density was 0.57 g / ml. Further, 0.077% of the hydrophobic substance (C) was present inside the water absorbent resin particles (8), and 0.005% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (8).

<Example 9>
“0.454 parts of material particles (D-1) obtained in Production Example 2” were changed to “0.248 parts of hydrophobic substance (C-3) {stearyl alcohol}”, and “apertures 150 and 850 μm” Absorbent resin particles (9) of the present invention were obtained in the same manner as in Example 1, except that the “screening of the sifter” was changed to “sieving with an opening of 355 and 850 μm” and adjusted to a particle size of 355 to 850 μm. The weight average particle diameter of the absorbent resin particles (9) was 600 μm, and the apparent density was 0.56 g / ml. Further, 0.156% of the hydrophobic substance (C) was present inside the water absorbent resin particles (9), and 0.008% of the hydrophobic substance (C) was present on the surface of the water absorbent resin particles (9).

<Example 10>
"Water-soluble vinyl monomer (a1-1) 155 parts (2.15 mole parts), crosslinking agent (b1) 0.6225 parts (0.0024 mole parts) and deionized water 340.27 parts" Monomer (a1-1) 155 parts (2.15 mol parts), cross-linking agent (b1) 0.6225 parts (0.0024 mol parts), hydrophobic substance (C-5) {low molecular weight polypropylene emulsion (Mitsui Chemicals, Inc.) Company product: Chemipearl WP100, concentration 40%: “Chemipearl” is a registered trademark of the company.) 4.728 parts and 33.541 parts of deionized water ”and“ Sieving with openings of 25 and 45 μm ” Was changed to “mesh of 125 and 710 μm openings” and adjusted to a particle size of 125 to 710 μm, in the same manner as in Production Example 1, to obtain absorbent resin particles (10) of the present invention. The weight average particle diameter of the absorbent resin particles (10) was 400 μm, and the apparent density was 0.59 g / ml. Further, 0.99% of the hydrophobic substance (C) was present inside the water-absorbent resin particles (10), and 0.01% of the hydrophobic substance (C) was present on the surface of the water-absorbent resin particles (10).

<Comparative Example 1>
A solution prepared by dissolving 0.004 parts of amino-modified silicone (Shin-Etsu Chemical Co., Ltd. product: KF354) in 80 parts of methanol was added to 40 parts of clay (ROCKWOOD ADDITIVES LIMITEDED: LAPONIPE XLG) and stirred at 25 ° C. for 2 minutes. Then, it dried at 60 degreeC * 1 hour, and obtained the material particle (D-7). The volume average particle diameter of the material particles (D-7) was 80 μm.

Next, in a glass reaction vessel, 77 parts of sodium acrylate, 22.85 parts of acrylic acid, 0.15 part of N, N′-methylenebisacrylamide and 293 parts of deionized water, dichlorotris (triphenylphosphine) ruthenium 0 0.001 part was charged, and the temperature of the contents was kept at 3 ° C. while stirring and mixing. After flowing nitrogen into the contents to make the dissolved oxygen amount 1 ppm or less, 0.3 part of 1% aqueous solution of hydrogen peroxide, 0.8 part of 0.2% aqueous solution of ascorbic acid and 2,2′-azobis Polymerization is started by adding and mixing 0.8 parts of a 2% aqueous solution of amidinopropane dihydrochloride, and after the reaction solution reaches 80 ° C., it is polymerized at a polymerization temperature of 80 ± 2 ° C. for about 5 hours. Gel (2) was obtained.
30 parts of the material particles (D-7) and 0.3 part of the surfactant (1) (manufactured by Sanyo Kasei Kogyo Co., Ltd .: Sanmorin OT70) are added to 300 parts of the hydrous gel (2). After kneading at 6 mm, 12 VR-400K manufactured by Iizuka Kogyo Co., Ltd. for 5 minutes at 25 ° C., the mixture was dried with an aeration-type band dryer under conditions of 135 ° C. and a wind speed of 2.0 m / sec to obtain a dried polymer product.
This polymer dried product was pulverized with a juicer mixer (Osterizer BLENDER manufactured by Oster) and adjusted to a particle size of 250 to 600 μm using a sieve having an opening of 250 and 600 μm, and then 100 parts of this polymer was stirred at a high speed (manufactured by Hosokawa Micron). 2 parts of a 10% water / methanol mixed solution of ethylene glycol diglycidyl ether (water / methanol weight ratio = 70/30) was added while being sprayed and mixed while the high-speed stirring turbulizer was rotated at 2000 rpm. Absorbent resin particles (H1) for comparison were obtained by allowing to stand at 140 ° C. for 30 minutes and crosslinking by heating. The weight average particle diameter of the absorbent resin particles (H1) was 390 μm, and the apparent density was 0.55 g / ml. Further, 0.005% of the hydrophobic substance (C) was present inside the water absorbent resin particles (10), and no hydrophobic substance (C) was present on the surface of the water absorbent resin particles (10).

<Comparative example 2>
"Material particle (D-7) 30 parts" was changed to "Material particles (D-8) {Silicon beads (Toshiba Silicone Co., Ltd .: Tospearl average particle size 2 μm)} 30 parts" and "Surfactant ( Comparative Example 1 except that 1) (Sanyo Kasei Kogyo Co., Ltd .: Sanmorin OT70) 0.3 part "was changed to" Surfactant (2) (Sanyo Kasei Kogyo Co., Ltd .: NAROACTY ID50) 0.3 part ". In the same manner, comparative absorbent resin particles (H2) were obtained. The weight average particle diameter of the absorbent resin particles (H2) was 390 μm, and the apparent density was 0.55 g / ml. Moreover, 39.0% of the hydrophobic substance (C) was present inside the water-absorbent resin particles (10), and 0.5% of the hydrophobic substance (C) was present on the surface of the water-absorbent resin particles (10).

  About the absorptive resin particles obtained in Examples 1 to 10 and Comparative Examples 1 and 2, the measured physical properties {weight average particle diameter, apparent density} and performance evaluation results {absorption amount by DW method, water retention amount, under load Absorption amount} is shown in Table 1. In Table 1, M1, M2, M3, and M4 represent the absorption amount after 1 minute by the DW method, the absorption amount after 2 minutes, the absorption amount after 5 minutes, and the absorption amount after 10 minutes, respectively. Indicates the content (% by weight) based on the weight of the crosslinked polymer (A1).

As can be seen from Table 1, the absorbent resin particles (Examples 1 to 10) of the present invention have an appropriate absorption rate pattern as compared with the absorbent resin particles of Comparative Examples 1 and 2.
Subsequently, when the absorption rate pattern was appropriate, it was evaluated what absorption characteristics were exhibited when applied to an absorbent article. Using the absorbent resin particles obtained in Examples 1 to 10 and Comparative Examples 1 and 2, absorbent articles (paper diapers) were prepared as follows, and the surface dryness value by the SDME method was evaluated. Are shown in Table 2.

<Preparation 1 of absorbent article (paper diaper)>
60 parts of fluff pulp and 140 parts of an evaluation sample {absorbent resin particles} were mixed with an airflow type mixing apparatus {Pad former manufactured by Autech Co., Ltd.} to obtain a mixture. laminated on m ² and so as to uniformly acrylic plate (thickness 4 mm), and pressed for 30 seconds at a pressure of 5 kg / cm ^2, to obtain absorbent body (1). This absorbent body (1) is cut into a 10 cm × 40 cm rectangle, and water absorbent paper (basis weight 15.5 g / m ² , manufactured by Advantech, filter paper No. 2) having the same size as the absorbent body is arranged above and below each. Further, a paper diaper (1) was prepared by disposing a polyethylene sheet (polyethylene film UB-1 manufactured by Tamapoly Co., Ltd.) on the back surface and a non-woven fabric (basis weight 20 g / m ² , Eltas Guard manufactured by Asahi Kasei Co., Ltd.) on the surface. The weight ratio of the absorbent resin particles to the fibers (weight of the absorbent resin particles / weight of the fibers) was 70/30.

<Preparation 2 of absorbent article (paper diaper)>
Preparation of absorbent article (paper diaper) 1 except that “60 parts fluff pulp and 140 parts evaluation sample {absorbent resin particles}” are changed to “20 parts fluff pulp and 180 parts evaluation sample {absorbent resin particles}” The paper diaper (2) was adjusted in the same manner as described above. The weight ratio of the absorbent resin particles and the fibers (weight of the absorbent resin particles / weight of the fibers) was 90/10.

<Surface dryness value by SDME method>
A disposable diaper {artificial urine (0.03% by weight of potassium chloride, 0.08% by weight of magnesium sulfate, 0.88% by weight of sodium sulfate, 0.8% by weight of sodium chloride) in which the detector of the SDME (Surface Dryness Measurement Equipment) tester (manufactured by WK system) is sufficiently moistened. % And deionized water 99.09% by weight) and a paper diaper was soaked for 60 minutes. }, A 0% dryness value was set, and then the detector of the SDME tester was prepared by drying a paper diaper {paper diaper at 80 ° C. for 2 hours by heating. } Was set to 100% dryness, and the SDME tester was calibrated. Next, set a metal ring (inner diameter 70 mm, length 50 mm) in the center of the paper diaper to be measured, inject 80 ml of artificial urine, and when the artificial urine has been absorbed {if the gloss due to artificial urine cannot be confirmed}, immediately Remove the metal ring, place three SDME detectors on the center of the paper diaper and its left and right sides (three places at equal intervals of 10 cm from the end of the 40 cm paper diaper), and start measuring the surface dryness value, 5 minutes after the start of the measurement Among the three SDME detectors, the dryness value of the central detector is the surface dryness value (1-1) {center}, and the dryness values of the remaining two SDME detectors are the surface dryness value (1-2). {Left}, surface dryness value (1-3) {right}.
The artificial urine, measurement atmosphere, and standing atmosphere were 25 ± 5 ° C. and 65 ± 10% RH.

  As can be seen from Table 2, the absorbent article using the absorbent resin particles of the present invention has a surface dryness value (1-1), (1- 2) and (1-3) were excellent with no bias. That is, the absorbent resin particles of the present invention have excellent absorption characteristics because they have a specific absorption rate pattern when applied to absorbent articles. Therefore, even if an absorbent article to which the absorbent resin particles of the present invention are applied is used, it is easily predicted that there is no concern about blurring or the like.

  The absorbent resin particles of the present invention can be applied to an absorbent body containing absorbent resin particles and a fibrous material, and absorbent articles {paper diapers, sanitary napkins, and medical blood retaining bodies comprising the absorbent body. It is useful for the agent}. In addition, pet urine absorbent, urine gelling agent for portable toilets, freshness preservation agent for fruits and vegetables, drip absorbent for meat and seafood, cooler, disposable warmer, battery gelling agent, water retention agent for plants and soil, dew condensation It can also be used in various applications such as inhibitors, water-stopping agents, packing agents and artificial snow.

DESCRIPTION OF SYMBOLS 1 Rubber stopper 2 Bullet part 3 Saline 4 Absorbent resin particle 5 Plain weave nylon mesh 6 Measuring stand 7 Cock 8 Cock 9 Intake pipe

Claims (12)

Absorbent resin particles comprising a water-soluble vinyl monomer (a1) and / or a hydrolyzable vinyl monomer (a2) and a crosslinked polymer (A1) having a crosslinking agent (b) as essential constituent units, The absorption amount (M1) after 1 minute by the DW (Demand Wettability) method of A1) is 14 to 19 ml / g, the absorption amount (M2) after 2 minutes is 26 to 33 ml / g, and after 5 minutes Absorbent resin particles having an absorption amount (M3) of 42 to 50 ml / g and an absorption amount (M4) after 10 minutes of 52 to 59 ml / g. Furthermore, it is an absorptive resin particle containing hydrophobic substance (C), Comprising: The absorptivity of Claim 1 which has a structure which contains a part or all of (C) inside an absorptive resin particle. Resin particles. The structure comprising part or all of the hydrophobic substance (C) inside the absorbent resin particle is hydrophobic on part or all of the surface of the hydrophilic material particle (d1) or the hydrophobic material particle (d2). The absorbent resin particle according to claim 2, wherein the absorbent resin particle has a structure comprising material particles (D) coated or impregnated with the substance (C) inside the absorbent resin particle. The hydrophilic material particles (d1) are crosslinked polymer (A2) particles having water-soluble vinyl monomer (a1) and / or hydrolyzable vinyl monomer (a2) and a crosslinking agent (b) as essential constituent units. Item 4. Absorbent resin particles according to Item 3. The absorbent resin particles according to claim 3 or 4, wherein the material particles (D) have a volume average particle diameter (µm) of 1 to 30. The absorbent resin particles according to any one of claims 3 to 5, wherein the content (% by weight) of the material particles (D) is 0.1 to 1.0 based on the weight of the crosslinked polymer (A1). The weight average particle diameter (micrometer) of an absorptive resin particle is 400-650, The absorptive resin particle in any one of Claims 1-6. Absorbent resin particles according to any one of claims 1 to 7, wherein the apparent density (g / ml) of the absorbent resin particles is 0.56 to 0.62. An absorbent comprising the absorbent resin particles according to any one of claims 1 to 8 and a fibrous material. The absorbent body according to claim 9, wherein the weight ratio of the absorbent resin particles to the fibers (weight of the absorbent resin particles / weight of the fibers) is 70/30 to 90/10. The absorbent article using the absorber of Claim 9 or 10. Hydrophobic substance (C) and water-containing gel of water-soluble vinyl monomer (a1) and / or hydrolyzable vinyl monomer (a2) and cross-linked polymer (A1) having internal cross-linking agent (b) as essential constituent units Mixing or kneading; and / or polymerization in the presence of the hydrophobic substance (C) with the water-soluble vinyl monomer (a1) and / or the hydrolyzable vinyl monomer (a2) and the internal cross-linking agent (b) as essential constituent units. A method for producing absorbent resin particles comprising a step of obtaining a hydrogel of a crosslinked polymer (A1),
The weight average particle diameter (μm) of the absorbent resin particles is 400 to 650, the apparent density (g / ml) of the absorbent resin particles is 0.56 to 0.62, and the DW (Demand) of the absorbent resin particles The absorption amount (M1) after 1 minute according to the Wettability method is 14 to 19 ml / g, the absorption amount after 2 minutes (M2) is 26 to 33 ml / g, and the absorption amount (M3) after 5 minutes is The manufacturing method of the absorbent resin particle which is 42-50 ml / g and the absorption amount (M4) after 10 minutes is 52-59 ml / g.

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