JPH1147588A - Liquid absorbing agent, absorptive article and their manufacture - Google Patents
Liquid absorbing agent, absorptive article and their manufactureInfo
- Publication number
- JPH1147588A JPH1147588A JP9209444A JP20944497A JPH1147588A JP H1147588 A JPH1147588 A JP H1147588A JP 9209444 A JP9209444 A JP 9209444A JP 20944497 A JP20944497 A JP 20944497A JP H1147588 A JPH1147588 A JP H1147588A
- Authority
- JP
- Japan
- Prior art keywords
- water
- blood
- amount
- resin
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 68
- 239000006096 absorbing agent Substances 0.000 title claims abstract description 64
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 210000004369 blood Anatomy 0.000 claims abstract description 150
- 239000008280 blood Substances 0.000 claims abstract description 150
- 239000011347 resin Substances 0.000 claims abstract description 127
- 229920005989 resin Polymers 0.000 claims abstract description 127
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 114
- 238000010521 absorption reaction Methods 0.000 claims abstract description 56
- 238000000034 method Methods 0.000 claims abstract description 9
- 239000002250 absorbent Substances 0.000 claims description 99
- 230000002745 absorbent Effects 0.000 claims description 42
- 239000000178 monomer Substances 0.000 abstract description 10
- 238000004132 cross linking Methods 0.000 abstract description 6
- 239000002245 particle Substances 0.000 abstract description 5
- 230000000379 polymerizing effect Effects 0.000 abstract description 3
- 239000000499 gel Substances 0.000 description 38
- 230000000052 comparative effect Effects 0.000 description 30
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 17
- -1 hydroxypropyl Chemical group 0.000 description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 15
- 229940048053 acrylate Drugs 0.000 description 15
- 238000010438 heat treatment Methods 0.000 description 12
- 239000003431 cross linking reagent Substances 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 241001494479 Pecora Species 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000000306 component Substances 0.000 description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 235000011187 glycerol Nutrition 0.000 description 8
- 210000000601 blood cell Anatomy 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 210000002700 urine Anatomy 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 239000000017 hydrogel Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
- WOAMRAPSJUZQJV-UHFFFAOYSA-N 3-oxopent-4-ene-2-sulfonic acid Chemical compound OS(=O)(=O)C(C)C(=O)C=C WOAMRAPSJUZQJV-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 229930195725 Mannitol Natural products 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 229940105990 diglycerin Drugs 0.000 description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 229920000578 graft copolymer Polymers 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000000594 mannitol Substances 0.000 description 2
- 235000010355 mannitol Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- MFEWNFVBWPABCX-UHFFFAOYSA-N 1,1,2,2-tetraphenylethane-1,2-diol Chemical compound C=1C=CC=CC=1C(C(O)(C=1C=CC=CC=1)C=1C=CC=CC=1)(O)C1=CC=CC=C1 MFEWNFVBWPABCX-UHFFFAOYSA-N 0.000 description 1
- ZZXUZKXVROWEIF-UHFFFAOYSA-N 1,2-butylene carbonate Chemical compound CCC1COC(=O)O1 ZZXUZKXVROWEIF-UHFFFAOYSA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- KFNAHVKJFHDCSK-UHFFFAOYSA-N 2-[2-(4,5-dihydro-1,3-oxazol-2-yl)ethyl]-4,5-dihydro-1,3-oxazole Chemical compound N=1CCOC=1CCC1=NCCO1 KFNAHVKJFHDCSK-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- AUZRCMMVHXRSGT-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid;prop-2-enamide Chemical compound NC(=O)C=C.CC(C)CS(O)(=O)=O AUZRCMMVHXRSGT-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- PUEFXLJYTSRTGI-UHFFFAOYSA-N 4,4-dimethyl-1,3-dioxolan-2-one Chemical compound CC1(C)COC(=O)O1 PUEFXLJYTSRTGI-UHFFFAOYSA-N 0.000 description 1
- LWLOKSXSAUHTJO-UHFFFAOYSA-N 4,5-dimethyl-1,3-dioxolan-2-one Chemical compound CC1OC(=O)OC1C LWLOKSXSAUHTJO-UHFFFAOYSA-N 0.000 description 1
- OVDQEUFSGODEBT-UHFFFAOYSA-N 4-methyl-1,3-dioxan-2-one Chemical compound CC1CCOC(=O)O1 OVDQEUFSGODEBT-UHFFFAOYSA-N 0.000 description 1
- AEYSASDBPHWTGR-UHFFFAOYSA-N 4-oxohex-5-ene-3-sulfonic acid Chemical compound CCC(S(O)(=O)=O)C(=O)C=C AEYSASDBPHWTGR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 206010021639 Incontinence Diseases 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000012503 blood component Substances 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- BRXCDHOLJPJLLT-UHFFFAOYSA-N butane-2-sulfonic acid Chemical compound CCC(C)S(O)(=O)=O BRXCDHOLJPJLLT-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 210000003756 cervix mucus Anatomy 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- VKONPUDBRVKQLM-UHFFFAOYSA-N cyclohexane-1,4-diol Chemical compound OC1CCC(O)CC1 VKONPUDBRVKQLM-UHFFFAOYSA-N 0.000 description 1
- VCVOSERVUCJNPR-UHFFFAOYSA-N cyclopentane-1,2-diol Chemical compound OC1CCCC1O VCVOSERVUCJNPR-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- CYKDLUMZOVATFT-UHFFFAOYSA-N ethenyl acetate;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=O)OC=C CYKDLUMZOVATFT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 235000020256 human milk Nutrition 0.000 description 1
- 210000004251 human milk Anatomy 0.000 description 1
- IHPDTPWNFBQHEB-UHFFFAOYSA-N hydrobenzoin Chemical compound C=1C=CC=CC=1C(O)C(O)C1=CC=CC=C1 IHPDTPWNFBQHEB-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 150000002918 oxazolines Chemical class 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 235000004252 protein component Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical compound O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 description 1
- 206010046901 vaginal discharge Diseases 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
Landscapes
- Absorbent Articles And Supports Therefor (AREA)
- Materials For Medical Uses (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、吸液剤、吸収性物
品およびそれらの製造方法に関する。特に、血液に対す
る吸収特性に優れた吸液剤、吸収性物品およびそれらの
製造方法に関する。The present invention relates to a liquid absorbing agent, an absorbent article, and a method for producing the same. In particular, the present invention relates to a liquid absorbing agent, an absorbent article, and a method for producing the same, which have excellent blood absorption properties.
【0002】[0002]
【従来の技術】近年、体液を吸収させることを目的と
し、紙おむつ、生理用ナプキンなどの衛生材料の構成材
料の一つとして吸水性樹脂が幅広く利用されている。上
記の吸水性樹脂としては、例えば、ポリアクリル酸部分
中和物架橋体、澱粉−アクリロニトリルグラフト重合体
の加水分解物、澱粉−アクリル酸グラフト重合体の中和
物、酢酸ビニル−アクリル酸エステル共重合体のケン化
物、アクリロニトリル共重合体もしくはアクリルアミド
共重合体の加水分解物またはこれらの架橋体、カチオン
性モノマーの架橋体などが知られている。2. Description of the Related Art In recent years, water-absorbent resins have been widely used as one of the constituent materials of sanitary materials such as disposable diapers and sanitary napkins for the purpose of absorbing body fluids. Examples of the water-absorbing resin include a crosslinked product of a partially neutralized polyacrylic acid, a hydrolyzate of a starch-acrylonitrile graft polymer, a neutralized product of a starch-acrylic acid graft polymer, and vinyl acetate-acrylate. A saponified polymer, a hydrolyzate of an acrylonitrile copolymer or an acrylamide copolymer, a crosslinked product thereof, a crosslinked product of a cationic monomer, and the like are known.
【0003】被吸収液が血液などの場合には、血液吸収
時に血液成分が個々の吸水性樹脂粒子を包囲し吸収を妨
げるために吸水性樹脂の吸引量が低下する等の特別の事
情があるため、尿に対する吸引量が高い吸水性樹脂であ
っても、血液に対する吸引量も高いとは限らない。この
ような事情に鑑み、吸水性樹脂の血液吸収特性を改良す
る試みとして、種々の提案がなされている。例えば、吸
水性樹脂の血液に対する吸収力改善を目的として、食塩
やポリエチレングリコールのような化合物を吸水性樹脂
に添加することが提案されている(特開昭58−501
107号公報、特開昭54−70694号公報)。ま
た、高吸水性繊維を不均一にすることにより衛生材料用
不織布の吸血率を向上させようとする試み(特開平6−
207358号公報)や、上層と下層をそれぞれ粒度の
異なる吸水性樹脂で構成した積層体(実開平6−589
52号公報)が提案されている。確かにこれらの構成と
することにより血液吸収特性は若干改善されるものの、
未だ実用上不十分なものであった。[0003] When the liquid to be absorbed is blood or the like, there are special circumstances such as a decrease in the amount of water-absorbing resin sucked because blood components surround individual water-absorbing resin particles during blood absorption and hinder absorption. Therefore, even if the water-absorbing resin has a high suction amount for urine, the suction amount for blood is not always high. In view of such circumstances, various proposals have been made as an attempt to improve the blood absorption characteristics of the water absorbent resin. For example, it has been proposed to add a compound such as salt or polyethylene glycol to a water-absorbing resin for the purpose of improving the absorbency of the water-absorbing resin against blood (Japanese Patent Laid-Open No. 58-501).
No. 107, JP-A-54-70694). Also, an attempt to improve the blood absorption rate of a nonwoven fabric for a sanitary material by making the superabsorbent fibers non-uniform (Japanese Unexamined Patent Publication No.
207358) and a laminate in which the upper layer and the lower layer are composed of water-absorbing resins having different particle sizes (Japanese Utility Model Application Laid-Open No. 6-589).
No. 52) has been proposed. Certainly, although the blood absorption characteristics are slightly improved by adopting these configurations,
It was still insufficient for practical use.
【0004】これを解決するものとして、国際公開96
−28515号公報では、羊血に対する血液面積率とい
う新規なパラメータを導入し、この血液面積率の高い吸
血液性樹脂組成物は優れた血液吸収特性を示すこと、ま
た吸水性樹脂の表面を高架橋することにより血液面積率
が高い吸血液性樹脂組成物が得られることが開示されて
いる。[0004] To solve this problem, International Publication No. 96
In Japanese Patent No. 28515, a new parameter of blood area ratio to sheep blood is introduced, a blood absorbing resin composition having a high blood area ratio exhibits excellent blood absorption properties, and the surface of the water absorbing resin is highly crosslinked. It discloses that a blood-absorbing resin composition having a high blood area ratio can be obtained.
【0005】[0005]
【発明が解決しようとする課題】国際公開96−285
15号公報に開示された技術によると、確かに血液吸収
特性はかなり改善されるものの、吸液剤が血液を二度以
上に分けて少量ずつ吸収した場合には、その合計で吸収
できる血液の量は一気に吸収する場合と比べて少なくな
ってしまうという問題があることがわかった。つまり、
吸液剤がいったん血液を吸収してゲル(血液ゲル)とな
ってしまうと、もはや本来吸収可能であったはずの量は
吸収できないのである。例えば、一気に血液を吸収すれ
ば10gの血液を吸収可能な吸液剤であっても、まず3
gの血液を吸収してからしばらく時間をおいて血液ゲル
となってしまった後には、さらに7gの血液を吸収する
ことは不可能となるのである。そのため、血液吸収量が
多い吸液剤であっても血液ゲル吸収性が悪ければ、せっ
かくの血液吸収量が多いという特徴は十分に生かされ
ず、結果として実用性に劣ったものとなってしまう。Problems to be Solved by the Invention International Publication No. 96-285
According to the technology disclosed in Japanese Patent Publication No. 15-175, although the blood absorption characteristics are considerably improved, when the liquid-absorbing agent absorbs blood twice or more little by little, the total amount of blood that can be absorbed is obtained. It has been found that there is a problem that the amount is reduced as compared with the case of absorbing at a stretch. That is,
Once the liquid-absorbing agent has absorbed the blood and turned into a gel (blood gel), the amount that could originally be absorbed can no longer be absorbed. For example, even if a liquid absorbing agent can absorb 10 g of blood if it absorbs blood at a stretch,
After the blood gel has been absorbed for a while after absorbing g of blood, it becomes impossible to absorb another 7 g of blood. Therefore, even if the liquid absorbing agent has a large amount of absorbed blood, if the blood gel absorbability is poor, the characteristic of having a large amount of absorbed blood cannot be fully utilized, resulting in poor practicality.
【0006】したがって、本発明の課題は、血液吸収量
および血液ゲル吸収量に優れた吸液剤、吸収性物品およ
びそれらの製造方法を提供することにある。Accordingly, an object of the present invention is to provide a liquid absorbing agent, an absorbent article, and a method for producing the same, which are excellent in blood absorption and blood gel absorption.
【0007】[0007]
【課題を解決するための手段】上記課題を解決するた
め、本発明は、以下の構成をとる。 (1) 血液ゲル吸収量が3g/g以上の吸液剤。 (2) 血液吸引量が5g/g以上の吸水性樹脂と、該吸水
性樹脂に対して20〜900重量%の水とを含有する吸
液剤。 (3) 血液吸引量が5g/g以上の吸水性樹脂と、該吸水
性樹脂に対して20〜900重量%の水とから吸液剤を
製造する方法。 (4) 含水率が15重量%未満であって血液吸引量が5g
/g以上の吸水性樹脂に水を加えて、含水率15重量%
以上とする吸液剤の製造方法。 (5) 血液吸引量が5g/g以上の吸水性樹脂と、該吸水
性樹脂に対して20〜900重量%の水とを含有する坪
量20〜10000g/m2の吸収性物品。 (6) 前記(1)または(2)記載の吸液剤を坪量20〜100
00g/m2で用いた吸収性物品。 (7) 血液吸引量が5g/g以上の吸水性樹脂と、該吸水
性樹脂に対して20〜900重量%の水とから坪量20
〜10000g/m2の吸収性物品を製造する方法。 (8) 含水率が15重量%未満であって血液吸引量が5g
/g以上の吸水性樹脂に水を加えて、含水率15重量%
以上とする、坪量20〜10000g/m2の吸収性物
品の製造方法。In order to solve the above problems, the present invention has the following arrangement. (1) A liquid absorbing agent having a blood gel absorption of 3 g / g or more. (2) A liquid-absorbing agent containing a water-absorbing resin having a blood suction amount of 5 g / g or more and 20 to 900% by weight of water with respect to the water-absorbing resin. (3) A method of producing a liquid-absorbing agent from a water-absorbing resin having a blood suction amount of 5 g / g or more and 20 to 900% by weight of water based on the water-absorbing resin. (4) The water content is less than 15% by weight and the blood suction amount is 5 g.
/ G or more of water-absorbent resin and water content of 15% by weight
A method for producing a liquid absorbing agent as described above. (5) An absorbent article having a basis weight of 20 to 10000 g / m 2 containing a water-absorbing resin having a blood suction amount of 5 g / g or more and water of 20 to 900% by weight based on the water-absorbing resin. (6) The liquid absorbing agent according to (1) or (2),
Absorbent article used at 00 g / m 2 . (7) A water-absorbent resin having a blood suction amount of 5 g / g or more and water having a basis weight of 20 to 900% by weight based on the water-absorbent resin.
Method of making an absorbent article ~10000g / m 2. (8) The water content is less than 15% by weight and the blood suction amount is 5 g
/ G or more of water-absorbent resin and water content of 15% by weight
A method for producing an absorbent article having a basis weight of 20 to 10000 g / m 2 as described above.
【0008】被吸収液が人工尿の場合には二度以上に分
けて吸液した場合と一度に吸液した場合とで吸液量にほ
とんど違いがなかったことから、血液ゲル吸収量の問題
は、血液等に特有の問題であると考えられる。本発明者
らは、血液の方が人工尿よりもゲルブロッキングを起こ
しやすいことも考え合わせて、人工尿と血液との一番大
きな違いは、血液は液体成分の他に固体成分である血球
等を含んでいることであると考え、血球等が血液ゲル吸
収性を阻害する原因であると推測した。さらに検討を進
め、血球の内部は水分であることから、血液が吸水性樹
脂に吸収される際に血球中の水分も吸水性樹脂に吸収さ
れ、血球の表面膜が吸水性樹脂表面に密着した状態で吸
水性樹脂がゲル化し、血球の表面膜によって吸水性樹脂
と新たな液体(血液)との接触が阻害されるのではない
かと考えた。そこで、血球の表面膜が吸水性樹脂に密着
しないようにするための手段として、特定量の水を吸水
性樹脂に吸収させることを考えつき、本発明に到達した
ものである。その作用機構は定かではないが、吸水性樹
脂が水を吸収することによって吸水性樹脂全体がほぼ均
一に少しだけゲル化するため、血液が吸水性樹脂の一部
だけに不均一に吸収される(ママコになる)という問題
が起こりにくくなるということや、水によって血液が希
釈されるために血液特有の問題が起きにくくなる等の理
由が考えられる。When the liquid to be absorbed is artificial urine, there is almost no difference in the amount of liquid absorbed between the case where the liquid is absorbed twice or more and the case where the liquid is absorbed at one time. Is considered to be a problem specific to blood and the like. The present inventors consider that blood is more likely to cause gel blocking than artificial urine.The biggest difference between artificial urine and blood is that blood is a solid component in addition to liquid components such as blood cells. Was considered to be the cause, and it was presumed that blood cells and the like were responsible for inhibiting blood gel absorbability. Further examination, since the inside of the blood cells is water, when the blood is absorbed by the water-absorbent resin, the water in the blood cells is also absorbed by the water-absorbent resin, the surface membrane of the blood cells adhered to the surface of the water-absorbent resin It was thought that the water-absorbent resin gelled in this state, and that the contact between the water-absorbent resin and the new liquid (blood) was hindered by the blood cell surface film. Then, as a means for preventing the surface film of blood cells from adhering to the water-absorbing resin, the present inventors have conceived of absorbing a specific amount of water into the water-absorbing resin, and have arrived at the present invention. The mechanism of action is unclear, but the water-absorbent resin absorbs water, causing the entire water-absorbent resin to gel slightly and almost uniformly, so that blood is unevenly absorbed by only a portion of the water-absorbent resin. Possible reasons are that the problem (become a mamako) is less likely to occur, and that the blood is diluted with water, so that problems unique to blood are less likely to occur.
【0009】[0009]
【発明の実施の形態】本発明の吸液剤について説明す
る。本発明の吸液剤は、血液ゲル吸収量が3g/g以上
であることを特徴とする。血液ゲル吸収量とは、後述の
実施例において定義されるものであり、吸液剤が血液を
吸収してゲルとなった状態での血液吸収量を定量するも
のである。血液ゲル吸収量が3g/g以上であると、吸
液剤が血液を二度以上にわけて少量ずつ吸収した場合で
も合計で吸収できる血液の量が十分に多くなる。血液ゲ
ル吸収量は好ましくは4g/g以上、より好ましくは
4.5g/g以上である。BEST MODE FOR CARRYING OUT THE INVENTION The liquid absorbing agent of the present invention will be described. The liquid absorbing agent of the present invention is characterized by having a blood gel absorption of 3 g / g or more. The blood gel absorption amount is defined in Examples described later, and is used to quantify the blood absorption amount in a state in which the liquid absorbing agent has absorbed the blood to form a gel. When the blood gel absorption amount is 3 g / g or more, the amount of blood that can be absorbed in total becomes sufficiently large even when the liquid absorbing agent absorbs the blood twice or more little by little. The blood gel absorption is preferably at least 4 g / g, more preferably at least 4.5 g / g.
【0010】血液ゲル吸収量の高い吸液剤としては、血
液吸引量が5g/g以上の吸水性樹脂と、該吸水性樹脂
に対して20〜900重量%の水とを含有するものが挙
げられる。血液吸引量とは、後述の実施例において定義
されるものであり、吸水性樹脂が血液を引く力を定量す
るものである。血液吸引量は5g/g以上であることが
好ましく、より好ましくは10g/g以上である。血液
吸引量を測定するための試料樹脂としては、重合して得
られる含水ゲル状重合体を必要に応じて表面架橋処理し
た吸水性樹脂を用いてもよいし、吸水性樹脂と水とを含
む吸液剤の水分を乾燥させてもう一度吸水性樹脂(含水
率15重量%未満)としたものを用いてもよい。Examples of the liquid absorbing agent having a high blood gel absorption include those containing a water-absorbing resin having a blood suction amount of 5 g / g or more and water in an amount of 20 to 900% by weight based on the water-absorbing resin. . The blood suction volume is defined in Examples described later, and is used to determine the force of the water-absorbing resin to draw blood. The blood suction amount is preferably 5 g / g or more, more preferably 10 g / g or more. As the sample resin for measuring the blood suction amount, a water-absorbent resin obtained by polymerizing a hydrogel polymer and subjecting it to surface cross-linking treatment as necessary, or including a water-absorbent resin and water It is also possible to use a water-absorbent resin (water content of less than 15% by weight) obtained by drying the water of the liquid absorbing agent.
【0011】なお、本明細書において、特に断らない限
り、「吸水性樹脂」とは水を全く含まない吸水性樹脂単
独のものだけでなく、水を15重量%未満の範囲で含む
ほぼ乾燥状態の吸水性樹脂をも含むものとする。吸液剤
が、血液吸引量が5g/g以上の吸水性樹脂に対し、2
0〜900重量%の水を含有することによって、血液吸
収量を低下させることなく血液ゲル吸収量を向上させる
ことができる。水の量が20重量%未満であると、血液
ゲル吸収量の向上が見られない。一方、水の量が900
重量%を越えると相対的な吸水性樹脂量が低下するた
め、血液吸収量が低下する。また同様の理由から水の効
果であるはずの血液ゲル吸収量の向上の度合いも低下す
る。また、吸液剤に含まれる吸水性樹脂の血液吸引量が
5g/g未満であると、水を20〜900重量%含んで
も血液ゲル吸収量の向上が見られない。吸水性樹脂の血
液吸引量は10g/g以上であることが好ましく、より
好ましくは12g/g以上である。また、水の量は好ま
しくは50〜400重量%、より好ましくは100〜2
00重量%である。In the present specification, unless otherwise specified, the term "water-absorbent resin" means not only a water-absorbent resin containing no water but also a substantially dry state containing water in a range of less than 15% by weight. Of water-absorbent resin. The water-absorbing agent is used for a water-absorbing resin having a blood suction amount of 5 g / g or more.
By containing 0 to 900% by weight of water, the blood gel absorption can be improved without lowering the blood absorption. If the amount of water is less than 20% by weight, no improvement in blood gel absorption is observed. On the other hand, if the amount of water is 900
If the content exceeds% by weight, the relative amount of the water-absorbing resin decreases, so that the amount of absorbed blood decreases. In addition, the degree of improvement in blood gel absorption, which should be the effect of water for the same reason, also decreases. In addition, if the water-absorbing resin contained in the liquid-absorbing agent has a blood suction amount of less than 5 g / g, no improvement in the blood gel absorption amount is observed even when the water-absorbing resin contains 20 to 900% by weight of water. The blood suction amount of the water absorbent resin is preferably 10 g / g or more, and more preferably 12 g / g or more. The amount of water is preferably 50 to 400% by weight, more preferably 100 to 2% by weight.
00% by weight.
【0012】なお、ここで血液吸収量とは、後述の実施
例において定義されるものであり、吸液剤が血液を吸収
する量を定量するものである。前述の血液吸引量では、
吸水性樹脂が血液を吸引する量そのものを表すのに対し
て、血液吸収量には、一旦吸引することができても吸液
剤中に保持できないものは含めない。したがって、衛生
材料の実用性の点からは、血液吸引量よりも血液吸収量
の方がより重要な因子であると言える。The amount of blood absorbed here is defined in the examples described later, and is used to determine the amount of the liquid absorbing agent that absorbs blood. In the aforementioned blood suction volume,
While the water-absorbing resin represents the amount of blood itself to be sucked, the amount of blood absorbed does not include those that can be once sucked but cannot be retained in the liquid absorbing agent. Therefore, it can be said that the amount of absorbed blood is a more important factor than the amount of sucked blood from the practicality of the sanitary material.
【0013】上記したような血液ゲル吸収量の高い吸液
剤は、血液吸引量が5g/g以上の吸水性樹脂と、該吸
水性樹脂に対して20〜900重量%の水とから製造す
ることができ、吸水性樹脂に対して水を後添加するのが
簡便である。含水率の観点から見ると、通常吸水性樹脂
の含水率は15重量%未満であるため、含水率が15重
量%未満であって血液吸引量が5g/g以上の吸水性樹
脂に水を加えて、含水率15重量%以上とすればよい。
ここで、含水率とは、吸水性樹脂と水の合計重量に対す
る水の重量の割合をいう。The above-mentioned liquid-absorbing agent having a high blood gel absorption amount is produced from a water-absorbing resin having a blood suction amount of 5 g / g or more and water in an amount of 20 to 900% by weight based on the water-absorbing resin. It is convenient to post-add water to the water-absorbent resin. From the viewpoint of the water content, the water content of the water-absorbent resin is usually less than 15% by weight. Therefore, water is added to the water-absorbent resin having a water content of less than 15% by weight and a blood suction amount of 5 g / g or more. Thus, the water content may be 15% by weight or more.
Here, the water content refers to the ratio of the weight of water to the total weight of the water absorbent resin and water.
【0014】本発明において用いられる吸水性樹脂とし
ては、水を吸収して体積膨張を起こすものであれば特に
制限はないが、一般に水溶性不飽和単量体を重合させる
ことにより得られる。これらの水溶性不飽和単量体の例
としては、(メタ)アクリル酸、(無水)マレイン酸、
フマル酸、クロトン酸、イタコン酸、2−(メタ)アク
リロイルエタンスルホン酸、2−(メタ)アクリロイル
プロパンスルホン酸、2−(メタ)アクリルアミド−2
−メチルプロパンスルホン酸、ビニルスルホン酸、スチ
レンスルホン酸等のアニオン性単量体やその塩;(メ
タ)アクリルアミド、N−置換(メタ)アクリルアミ
ド、2−ヒドロキシエチル(メタ)アクリレート、2−
ヒドロキシプロピル(メタ)アクリレート、メトキシポ
リエチレングリコール(メタ)アクリレート、ポリエチ
レングリコール(メタ)アクリレート等のノニオン性親
水基含有単量体、N,N−ジメチルアミノエチル(メ
タ)アクリレート、N,N−ジメチルアミノプロピル
(メタ)アクリレート、N,N−ジメチルアミノプロピ
ル(メタ)アクリルアミド等のアミノ基含有不飽和単量
体やそれらの4級化物等を具体的に挙げることができ
る。また、得られる重合体の親水性を極度に阻害しない
程度の量で、例えば、メチル(メタ)アクリレート、エ
チル(メタ)アクリレート、ブチル(メタ)アクリレー
ト等のアクリル酸エステル類や酢酸ビニル、プロピオン
酸ビニル等の疎水性単量体を使用してもよい。単量体成
分としてはこれらのうちから1種または2種以上を選択
して用いることができるが、最終的に得られる吸水性材
料の吸水諸特性を考えると(メタ)アクリル酸(塩)、
2−(メタ)アクリロイルエタンスルホン酸(塩)、2
−(メタ)アクリルアミド−2−メチルプロパンスルホ
ン酸(塩)、(メタ)アクリルアミド、メトキシポリエ
チレングリコール(メタ)アクリレート、N,N−ジメ
チルアミノエチル(メタ)アクリレートまたはその4級
化物からなる群から選ばれる1種以上のものが好まし
く、(メタ)アクリル酸(塩)を必須成分として含むも
のがさらに好ましい。この場合(メタ)アクリル酸の3
0〜90モル%が塩基性物質で中和されているものが最
も好ましい。また、吸水性樹脂としての吸水倍率は、生
理食塩水中のティーバッグ法による値で、20〜60g
/g程度有することが好ましい。未架橋成分、いわゆる
水可溶成分の割合は20重量%以下が好ましく、より好
ましくは10重量%以下、さらに少ないほど好ましい。The water-absorbing resin used in the present invention is not particularly limited as long as it absorbs water and causes volume expansion, but is generally obtained by polymerizing a water-soluble unsaturated monomer. Examples of these water-soluble unsaturated monomers include (meth) acrylic acid, (maleic anhydride),
Fumaric acid, crotonic acid, itaconic acid, 2- (meth) acryloylethanesulfonic acid, 2- (meth) acryloylpropanesulfonic acid, 2- (meth) acrylamide-2
Anionic monomers such as methylpropanesulfonic acid, vinylsulfonic acid and styrenesulfonic acid and salts thereof; (meth) acrylamide, N-substituted (meth) acrylamide, 2-hydroxyethyl (meth) acrylate, 2-
Nonionic hydrophilic group-containing monomers such as hydroxypropyl (meth) acrylate, methoxypolyethylene glycol (meth) acrylate, and polyethylene glycol (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylate, N, N-dimethylamino Specific examples thereof include amino group-containing unsaturated monomers such as propyl (meth) acrylate and N, N-dimethylaminopropyl (meth) acrylamide, and quaternized products thereof. In addition, in an amount that does not extremely impair the hydrophilicity of the obtained polymer, for example, acrylates such as methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, vinyl acetate, and propionic acid A hydrophobic monomer such as vinyl may be used. One or more of these can be selected and used as the monomer component. However, considering the water absorption properties of the finally obtained water absorbing material, (meth) acrylic acid (salt),
2- (meth) acryloylethanesulfonic acid (salt), 2
Selected from the group consisting of-(meth) acrylamide-2-methylpropanesulfonic acid (salt), (meth) acrylamide, methoxypolyethylene glycol (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylate or a quaternized product thereof. Preferably, one or more of these are included, and more preferably those containing (meth) acrylic acid (salt) as an essential component. In this case, (meth) acrylic acid 3
Most preferably, 0 to 90 mol% is neutralized with a basic substance. The water absorption capacity as a water-absorbing resin is 20 to 60 g as a value according to a tea bag method in physiological saline.
/ G. The proportion of the uncrosslinked component, the so-called water-soluble component, is preferably 20% by weight or less, more preferably 10% by weight or less, and the smaller the ratio, the better.
【0015】また、吸水性樹脂は、架橋剤を使用せずに
得られる自己架橋型のものでも、重合性不飽和基および
/または反応性官能基を有する架橋剤を、得られる吸水
性樹脂の諸特性が所望の基準に達する範囲で用いて得ら
れるものでもよい。この場合、吸水性樹脂内部の架橋に
用いられる内部架橋剤の例としては、例えばN,N’−
メチレンビス(メタ)アクリルアミド、(ポリ)エチレ
ングリコール(メタ)アクリレート、グリセリントリ
(メタ)アクリレート、トリメチロールプロパントリ
(メタ)アクリレート、トリアリルアミン、トリアリル
シアヌレート、トリアリルイソシアヌレート、グリシジ
ル(メタ)アクリレート、(ポリ)エチレングリコー
ル、ジエチレングリコール、(ポリ)グリセリン、プロ
ピレングリコール、ジエタノールアミン、トリメチロー
ルプロパン、ペンタエリスリトール、(ポリ)エチレン
グリコールジグリシジルエーテル、(ポリ)グリセロー
ル(ポリ)グリシジルエーテル、エピクロルヒドリン、
エチレンジアミン、ポリエチレンイミン、(ポリ)塩化
アルミニウム、硫酸アルミニウム、塩化カルシウム、硫
酸マグネシウム等を具体的に挙げることができる。これ
らのうち反応性を考慮して、1種または2種以上を用い
ることができる。The water-absorbing resin may be a self-crosslinking type obtained without using a cross-linking agent, or a cross-linking agent having a polymerizable unsaturated group and / or a reactive functional group may be used. It may be obtained by using various characteristics in a range that reaches a desired standard. In this case, examples of the internal crosslinking agent used for crosslinking inside the water absorbent resin include, for example, N, N′-
Methylenebis (meth) acrylamide, (poly) ethylene glycol (meth) acrylate, glycerin tri (meth) acrylate, trimethylolpropane tri (meth) acrylate, triallylamine, triallyl cyanurate, triallyl isocyanurate, glycidyl (meth) acrylate , (Poly) ethylene glycol, diethylene glycol, (poly) glycerin, propylene glycol, diethanolamine, trimethylolpropane, pentaerythritol, (poly) ethylene glycol diglycidyl ether, (poly) glycerol (poly) glycidyl ether, epichlorohydrin,
Specific examples thereof include ethylenediamine, polyethyleneimine, (poly) aluminum chloride, aluminum sulfate, calcium chloride, and magnesium sulfate. Among these, one or two or more can be used in consideration of reactivity.
【0016】吸水性樹脂の平均粒子径は特に限定されな
いが、10〜400μmの範囲が好ましく、得られる吸
水性樹脂の血液吸収諸特性を考えると、20〜100μ
mが特に好ましい。吸水性樹脂の表面近傍を架橋処理す
ることにより、吸水性樹脂の血液吸引量および血液吸収
量を高めることができる。表面架橋剤としては、吸水性
樹脂の表面の官能基と反応できる2個以上の官能基を有
するもので、生理用ナプキン等の吸収性物品に使用した
場合安全性の高いものが好ましく、例えば、エチレング
リコール、ジエチレングリコール、トリエチレングリコ
ール、ポリエチレングリコール、プロピレングリコー
ル、ポリプロピレングリコール、トリメチレングリコー
ル、1,3−プロパンジオール、1,4−ブタンジオー
ル、1,5−ペンタンジオール、1,6−ヘキサンジオ
ール、1,7−ヘプタンジオール、1,8−オクタンジ
オール、1,9−ノナンジオール、ピナコール、ヒドロ
ベンゾイン、ベンズピナコール、シクロペンタン−1,
2−ジオール、シクロヘキサン−1,4−ジオール、ペ
ンタエリスリトール、グリセリン、ジグリセリン、ポリ
グリセリン、ジエタノールアミン、トリエタノールアミ
ン、ポリオキシプロピレン、オキシエチレン−オキシプ
ロピレンブロックポリマー、ソルビット、ソルビタン、
ソルビタン脂肪酸エステル、ポリオキシエチレンソルビ
タン脂肪酸エステル、トリメチロールプロパン、ペンタ
エリトリット、ポリビニルアルコール、グルコース、マ
ンニット、マンニタン、ショ糖、ブドウ糖等の多価アル
コール;エチレンカーボネート、プロピレンカーボネー
ト、4,5−ジメチル−1,3−ジオキソラン−2−オ
ン、4,4−ジメチル−1,3−ジオキソラン−2−オ
ン、4−エチル−1,3−ジオキソラン−2−オン、4
−ヒドロキシメチル−1,3−ジオキソラン−2−オ
ン、1,3−ジオキサン−2−オン、4−メチル−1,
3−ジオキサン−2−オン、4,6−ジメチル−1,3
−ジオキサン−2−オン等のアルキレンカーボネート;
エチレンジアミン、ジエチレントリアミン、トリエチレ
ンテトラミン、テトラエチレンペンタミン、ペンタエチ
レンヘキサミン、ポリエチレンイミン等の多価アミン;
2,4−トリレンジイソシアネート、ヘキサメチレンジ
イソシアネート等の多価イソシアネート;1,2−エチ
レンビスオキサゾリン等の多価オキサゾリン;2,2−
ビスヒドロキシメチルブタノール−トリス[3−(1−
アジリジル)プロピオネート]、1,6−ヘキサメチレ
ンジエチレンウレア、ジフェニルメタン−ビス−4,
4’−N,N’−ジエチレンウレア等の多価アジリジン
等が挙げられる。表面架橋剤としては、これらのうちの
1種または2種以上を用いることができる。中でも、得
られる吸水性樹脂の血液吸引量および血液吸収量の観点
から多価アルコールおよびアルキレンカーボネートが好
ましく、エチレングリコール、ジエチレングリコール、
トリエチレングリコール、ポリエチレングリコール、プ
ロピレングリコール、グリセリン、ジグリセリン、ポリ
グリセリン、エチレンカーボネート、プロピレンカーボ
ネートが好ましく、グリセリンが最も好ましい。The average particle size of the water-absorbent resin is not particularly limited, but is preferably in the range of 10 to 400 μm.
m is particularly preferred. By crosslinking the vicinity of the surface of the water-absorbent resin, it is possible to increase the blood suction amount and the blood absorption amount of the water-absorbent resin. As the surface cross-linking agent, those having two or more functional groups capable of reacting with the functional groups on the surface of the water-absorbent resin, those having high safety when used in absorbent articles such as sanitary napkins are preferable, for example, Ethylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol, trimethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, pinacol, hydrobenzoin, benzpinacol, cyclopentane-1,
2-diol, cyclohexane-1,4-diol, pentaerythritol, glycerin, diglycerin, polyglycerin, diethanolamine, triethanolamine, polyoxypropylene, oxyethylene-oxypropylene block polymer, sorbit, sorbitan,
Polyhydric alcohols such as sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, trimethylolpropane, pentaerythritol, polyvinyl alcohol, glucose, mannitol, mannitol, sucrose, glucose; ethylene carbonate, propylene carbonate, 4,5-dimethyl -1,3-dioxolan-2-one, 4,4-dimethyl-1,3-dioxolan-2-one, 4-ethyl-1,3-dioxolan-2-one,
-Hydroxymethyl-1,3-dioxolan-2-one, 1,3-dioxan-2-one, 4-methyl-1,
3-dioxan-2-one, 4,6-dimethyl-1,3
Alkylene carbonates such as -dioxan-2-one;
Polyvalent amines such as ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine and polyethyleneimine;
Polyvalent isocyanates such as 2,4-tolylene diisocyanate and hexamethylene diisocyanate; polyvalent oxazolines such as 1,2-ethylenebisoxazoline; 2,2-
Bishydroxymethylbutanol-tris [3- (1-
Aziridyl) propionate], 1,6-hexamethylenediethyleneurea, diphenylmethane-bis-4,
And polyvalent aziridine such as 4'-N, N'-diethyleneurea. One or more of these can be used as the surface crosslinking agent. Among them, polyhydric alcohols and alkylene carbonates are preferable from the viewpoints of blood suction amount and blood absorption amount of the obtained water-absorbent resin, ethylene glycol, diethylene glycol,
Triethylene glycol, polyethylene glycol, propylene glycol, glycerin, diglycerin, polyglycerin, ethylene carbonate, propylene carbonate are preferred, and glycerin is most preferred.
【0017】表面架橋剤の使用量は特に限定されない
が、吸水性樹脂100重量部に対して0.5〜10重量
部の範囲が好ましく、さらに好ましくは2〜5重量部の
範囲である。使用量が0.5重量部未満では、たとえ長
時間加熱しても得られる吸液剤の血液吸引量および血液
吸収量が上がりにくい。一方、使用量が10重量部を越
えると、使用量の増加に相当する効果を得ることは困難
であり、さらに未反応物が残存し、そのため種々のトラ
ブルの原因となるばかりでなく不経済である。The amount of the surface crosslinking agent to be used is not particularly limited, but is preferably in the range of 0.5 to 10 parts by weight, more preferably 2 to 5 parts by weight, per 100 parts by weight of the water-absorbent resin. If the amount used is less than 0.5 part by weight, the amount of blood absorption and blood absorption of the liquid absorbing agent obtained even if heated for a long time is unlikely to increase. On the other hand, if the amount used exceeds 10 parts by weight, it is difficult to obtain an effect corresponding to an increase in the amount used, and further unreacted substances remain, which not only causes various troubles but also is uneconomical. is there.
【0018】前記吸水性樹脂に表面架橋処理を施すに
は、通常、吸水性樹脂と表面架橋剤を均一に混合後、造
粒したものを加熱処理する。吸水性樹脂と表面架橋剤の
混合を均一にするには、吸水性樹脂100重量部に対
し、水0〜50重量部および親水性有機溶媒0〜60重
量部を用いてもよい。親水性有機溶媒としては、メタノ
ール、エタノール、n−プロパノール、イソプロパノー
ル、n−ブタノール、イソブタノール、sec−ブタノ
ールおよびt−ブタノールのような低級アルコール類、
アセトン、メチルエチルケトン、メチルイソブチルケト
ンのようなエーテル類、ジオキサン、テトラヒドロフラ
ンおよびジエチルエーテルのようなエーテル類、N,N
−ジメチルホルムアミドおよびN,N−ジエチルホルム
アミドのようなアミド類およびジメチルスルホキシドの
ようなスルホキシド類が挙げられる。In order to subject the water-absorbent resin to the surface cross-linking treatment, usually, the water-absorbent resin and the surface cross-linking agent are uniformly mixed, and the granulated product is heated. To make the mixing of the water-absorbing resin and the surface crosslinking agent uniform, 0 to 50 parts by weight of water and 0 to 60 parts by weight of the hydrophilic organic solvent may be used with respect to 100 parts by weight of the water-absorbing resin. As the hydrophilic organic solvent, lower alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol and t-butanol,
Ethers such as acetone, methyl ethyl ketone, methyl isobutyl ketone, ethers such as dioxane, tetrahydrofuran and diethyl ether, N, N
Amides such as -dimethylformamide and N, N-diethylformamide and sulfoxides such as dimethylsulfoxide.
【0019】混合方法は特に制限されず、通常の混合機
を用いることができる。また、造粒方法は特に制限され
ないが、押し出し造粒法が好ましい。加熱処理は、表面
架橋剤として多価アルコールまたはアルキレンカーボネ
ートを使用する場合、被加熱物の温度および加熱処理時
間が下記式(1)に示される条件下で行うのが好まし
い。The mixing method is not particularly limited, and an ordinary mixer can be used. The granulation method is not particularly limited, but extrusion granulation is preferred. When a polyhydric alcohol or an alkylene carbonate is used as the surface cross-linking agent, the heat treatment is preferably performed under the conditions of the temperature of the object to be heated and the heat treatment time represented by the following formula (1).
【0020】 log(t)≧15.7×103(1/T)−24.4 (1) (式中、tは加熱処理時間(秒)であり、Tは被加熱物
の絶対温度(K)である。) 式(1)を満足しない条件で加熱処理を行うと血液吸引
量および血液吸収量の劣ったものとなる。さらに、下記
式(2)に示される条件下で行うのが好ましい。Log (t) ≧ 15.7 × 10 3 (1 / T) −24.4 (1) (where, t is a heat treatment time (second), and T is an absolute temperature of an object to be heated ( If the heat treatment is performed under conditions that do not satisfy the expression (1), the blood suction amount and the blood absorption amount will be inferior. Further, it is preferable to carry out the reaction under the condition represented by the following formula (2).
【0021】 15.7×103(1/T)−23≧ log(t)≧15.7×103(1/T)−24.4 (2) (式中、tは加熱処理時間(秒)であり、Tは被加熱物
の絶対温度(K)である。) 式(2)を満足しない条件で加熱処理を行うと、長時間
費やしたことに相当する効果を得ることは困難であり不
経済である。15.7 × 10 3 (1 / T) −23 ≧ log (t) ≧ 15.7 × 10 3 (1 / T) −24.4 (2) (where t is the heat treatment time ( Second) and T is the absolute temperature (K) of the object to be heated.) If the heat treatment is performed under conditions not satisfying the expression (2), it is difficult to obtain an effect equivalent to spending a long time. It is uneconomical.
【0022】表面架橋剤が多価アルコールまたはアルキ
レンカーボネートである場合、具体的な被加熱物の温度
および加熱処理時間としては、170℃で18時間以上
70時間以下〜250℃で5分以上18分以下が好まし
く、180℃で8時間以上30時間以下〜210℃で1
時間以上3時間以下がより好ましい。被加熱物の温度が
170℃未満であると、血液吸引量および血液吸収量の
高いものを得るために非常に長い時間がかかり経済的で
ない。一方、被加熱物の温度が250℃を越えるもので
あると、使用される吸水性樹脂の種類によっては熱劣化
を起こす危険性がある。When the surface cross-linking agent is a polyhydric alcohol or an alkylene carbonate, the temperature of the object to be heated and the heat treatment time are from 18 to 70 hours at 170 ° C. to 5 to 18 minutes at 250 ° C. Or less, preferably at 180 ° C for 8 hours or more and 30 hours or less to 210 ° C for 1 hour.
The time is more preferably from 3 hours to 3 hours. If the temperature of the object to be heated is lower than 170 ° C., it takes a very long time to obtain a high blood suction amount and a high blood absorption amount, which is not economical. On the other hand, if the temperature of the object to be heated exceeds 250 ° C., there is a risk of causing thermal degradation depending on the type of the water-absorbing resin used.
【0023】本発明の加熱方法は、特に制限されるもの
ではなく、通常の乾燥機や加熱炉、例えば溝型攪拌乾燥
機、回転乾燥機、流動層乾燥機、気流乾燥機、赤外線乾
燥機、誘電加熱等を用いることができる。この加熱処理
の際の剪断力や破砕力はできるだけ小さい方が、血液吸
引量や血液吸収量の優れたものを得るために好ましく、
上記の中で流動層乾燥機、気流乾燥機が好ましい。The heating method of the present invention is not particularly limited, and may be a conventional dryer or heating furnace, for example, a channel-type stirring dryer, a rotary dryer, a fluidized-bed dryer, a flash dryer, an infrared dryer, Dielectric heating or the like can be used. It is preferable that the shearing force and the crushing force at the time of this heat treatment be as small as possible in order to obtain an excellent blood suction amount and blood absorption amount,
Among the above, a fluidized bed dryer and a flash dryer are preferred.
【0024】本発明の吸収性物品について説明する。吸
収性物品とは、吸水性樹脂を親水性繊維等の必要な部材
と組み合わせて構成したものである。本発明の吸収性物
品は、血液吸引量が5g/g以上の吸水性樹脂と、該吸
水性樹脂に対して20〜900重量%の水を含む。この
ような吸収性物品を製造するには、前記条件を満たす吸
水性樹脂と水とから製造すればよく、組み合わせる順番
等は特に限定されるわけではないが、例えば、次のよう
な方法が挙げられる。The absorbent article of the present invention will be described. The absorbent article is formed by combining a water-absorbing resin with necessary members such as hydrophilic fibers. The absorbent article of the present invention contains a water-absorbing resin having a blood suction amount of 5 g / g or more, and 20 to 900% by weight of water based on the water-absorbing resin. In order to manufacture such an absorbent article, it may be manufactured from a water-absorbent resin and water satisfying the above conditions, and the order of combination and the like are not particularly limited, but examples include the following method. Can be
【0025】上述した吸液剤を親水性繊維等と組み合
わせる。 吸水性樹脂を親水性繊維等と組み合わせた後に水を添
加する。 親水性繊維等に水を加えた後、吸水性樹脂と組み合わ
せる。 また、含水率の観点から見た場合、吸液剤の説明で述べ
たのと同様に、含水率が15重量%未満であって血液吸
引量が5g/g以上の吸水性樹脂に水を加えて、含水率
15重量%以上とすればよい。坪量は20〜10000
g/m2の範囲が一般的であり、100〜1000g/
m2の範囲が好ましく、200〜600g/m2の範囲が
より好ましい。The above-mentioned liquid absorbing agent is combined with a hydrophilic fiber or the like. Water is added after the water-absorbing resin is combined with the hydrophilic fiber or the like. After water is added to the hydrophilic fiber or the like, it is combined with a water-absorbing resin. Further, from the viewpoint of the water content, as described in the description of the liquid absorbing agent, water is added to a water-absorbing resin having a water content of less than 15% by weight and a blood suction amount of 5 g / g or more. The water content may be 15% by weight or more. Basis weight 20 to 10000
g / m < 2 > is common, and 100-1000 g / m <2>.
The range of m 2 is preferable, and the range of 200 to 600 g / m 2 is more preferable.
【0026】本発明の吸収性物品に用いられる親水性繊
維としては、公知のものがいずれも使用できる。例え
ば、粉砕された木材パルプ、コットンリンターや架橋セ
ルロース繊維、レーヨン、綿、羊毛、アセテート、ビニ
ロン等を用いることができる。中でも、粉砕された木材
パルプのエアレイド・パッドの形のものが好ましい。本
発明の吸収性物品は、拡散層、脚部弾性部材、腰部弾性
部材、テープなど公知の多数の部材を具備していてもよ
い。As the hydrophilic fiber used for the absorbent article of the present invention, any known fibers can be used. For example, pulverized wood pulp, cotton linter, crosslinked cellulose fiber, rayon, cotton, wool, acetate, vinylon, and the like can be used. Among them, those in the form of air-laid pads of ground wood pulp are preferred. The absorbent article of the present invention may include a number of known members such as a diffusion layer, a leg elastic member, a waist elastic member, and a tape.
【0027】本発明の吸収性物品は、上述したように血
液に対して優れた吸収特性を示すものであるが、その
他、血液と同様にタンパク質成分を含む水、例えば、牛
乳、母乳、おりもの等に対しても優れた吸収特性を示
す。また、従来の吸水性樹脂と同様の尿、海水、セメン
ト水、土壌水、肥料含有水、雨水、排水等に対しても優
れた吸収特性を示す。具体的な用途として、生理用ナプ
キン、タンポン、医療用血液吸収性物品、創傷保護材、
創傷治癒材、手術用廃液処理剤等の血液吸収特性の要求
される用途の他、使い捨ておむつや失禁パット等の衛生
材料、土木、農園芸等の各種産業分野においても好適に
用いられる。さらに、本発明の吸液剤または吸収性物品
に消臭剤、香料、薬剤、植物生育助剤、殺菌剤、発泡
剤、顔料、染料、親水性短繊維、肥料等を介在させるこ
とにより、得られる吸液剤に新たな機能を付与すること
もできる。The absorbent article of the present invention exhibits excellent absorption characteristics for blood as described above, but also contains water containing protein components like blood, for example, milk, breast milk, and vaginal discharge. It also shows excellent absorption characteristics for the same. In addition, it exhibits excellent absorption characteristics to urine, seawater, cement water, soil water, fertilizer-containing water, rainwater, drainage, and the like, similar to conventional water-absorbent resins. Specific applications include sanitary napkins, tampons, medical blood-absorbing articles, wound protectors,
In addition to applications requiring blood absorption properties, such as wound healing materials and treatment liquid for surgical use, it is also suitably used in various industrial fields such as sanitary materials such as disposable diapers and incontinence pads, civil engineering, and agricultural and horticultural arts. Furthermore, it can be obtained by interposing a deodorant, a fragrance, a drug, a plant growth aid, a bactericide, a foaming agent, a pigment, a dye, a hydrophilic short fiber, a fertilizer, etc. in the liquid absorbing agent or the absorbent article of the present invention. A new function can be given to the liquid absorbing agent.
【0028】[0028]
【実施例】以下、実施例および比較例により、本発明を
さらに詳細に説明するが、本発明はこれらにより何ら限
定されるものではない。なお、実施例中で「部」とは特
にことわりがない限り「重量部」を表すものとする。The present invention will be described in more detail with reference to the following Examples and Comparative Examples, but the present invention is not limited thereto. In the examples, “parts” means “parts by weight” unless otherwise specified.
【0029】吸液剤の諸性能は以下の方法により測定し
た。 (a)血液吸引量 内径95mmのシャーレ中の羊血(緬羊脱繊維血液;日
本バイオテスト研究所製、以下同じ)20mlに浸した
16枚重ねのトイレットペーパー(55mm×75m
m)上に試料樹脂約1gを加え、5分間吸液させた後、
膨潤ゲルを採取してその重量を測定した。吸液後の膨潤
ゲルの重量を元の試料樹脂の重量で除して、試料樹脂の
血液吸引量(g/g)を算出した。 (b)血液吸収量 内径60mmのシャーレ中に試料樹脂1gをできるだけ
均一にまき、その上に羊血5gを滴下し、血液を吸った
ゲルとする。ほとんどの吸水性樹脂はこの状態で均一な
ゲルにはならない。Various properties of the liquid absorbing agent were measured by the following methods. (A) Blood Suction Volume 16 sheets of toilet paper (55 mm × 75 m) immersed in 20 ml of sheep blood (sheep defibrillated blood; manufactured by Japan Biotest Laboratory, the same applies hereinafter) in a petri dish having an inner diameter of 95 mm
m) Approximately 1 g of the sample resin is added on the top, and after absorbing for 5 minutes,
The swollen gel was collected and its weight was measured. The weight of the swollen gel after absorption was divided by the weight of the original sample resin to calculate the blood suction amount (g / g) of the sample resin. (B) Amount of absorbed blood 1 g of the sample resin is spread as uniformly as possible in a Petri dish having an inner diameter of 60 mm, and 5 g of sheep blood is dropped thereon to obtain a gel that has absorbed blood. Most water absorbent resins do not form a uniform gel in this state.
【0030】次に、5分放置後、キッチンタオル(10
枚重ね)をそのゲルの上に置き、その上に重り(荷重0.
7psi=49g/cm2)を乗せ、1分後のキッチンタオルの重量
を測定し、その重量変化を、滴下した羊血から引いた値
を血液吸収量とした。 (c)血液ゲル吸収量 内径60mmのシャーレ中に試料樹脂1gをできるだけ
均一にまき、その上に羊血5gを滴下し、血液を吸った
ゲルとする。Then, after leaving for 5 minutes, a kitchen towel (10
Place the gel on the gel and put a weight on it (load 0.
7 psi = 49 g / cm 2 ), and the weight of the kitchen towel one minute later was measured, and the change in the weight was subtracted from the dropped sheep blood to determine the blood absorption. (C) Absorption of blood gel 1 g of the sample resin is spread as uniformly as possible in a petri dish having an inner diameter of 60 mm, and 5 g of sheep blood is dropped thereon to obtain a blood-sucking gel.
【0031】60分放置後、上記血液を吸ったゲルに羊
血を5g滴下し、5分放置後、キッチンタオル(10枚
重ね)を前記ゲルの上に置き、その上に重り(荷重0.7p
si=49g/cm2)を乗せ、1分後のキッチンタオルの重量を
測定し、その重量変化を、滴下した羊血から引いた値を
血液ゲル吸収量とした。 (d)血液戻り量 吸収性物品の中心部に羊血約15gを注射器で滴下し、
約5分間経過後、吸収性物品の表面を手で触って戻り量
を評価し、それを血液戻り量とした。さらに、1時間
経過後、羊血15gを注射器で滴下し、約5分経過後、
吸収性物品の表面を手で触って戻り量を評価し、それを
血液戻り量とした。 [実施例1]カルボキシル基を有する吸水性樹脂の製造
に際して、単量体成分としてのアクリル酸ナトリウム
(中和率75モル%)の37重量%水溶液4400部
に、内部架橋剤としてのトリメチロールプロパントリア
クリレート2.72部を溶解させて反応液とした。次
に、この反応液を窒素ガス雰囲気下で30分間脱気し
た。After standing for 60 minutes, 5 g of sheep blood was dropped on the gel that absorbed the blood, and after standing for 5 minutes, a kitchen towel (10 sheets) was placed on the gel, and a weight (0.7 p.
si = 49 g / cm 2 ), the weight of the kitchen towel one minute later was measured, and the change in the weight was subtracted from the dropped sheep blood to obtain the blood gel absorption amount. (D) Blood return amount About 15 g of sheep blood is dropped on the central part of the absorbent article with a syringe,
After a lapse of about 5 minutes, the amount of return was evaluated by touching the surface of the absorbent article with the hand, and this was defined as the amount of blood returned. Further, after 1 hour, 15 g of sheep blood is dropped with a syringe, and after about 5 minutes,
The amount of return was evaluated by touching the surface of the absorbent article with the hand, and this was defined as the amount of blood returned. [Example 1] In the production of a water-absorbent resin having a carboxyl group, trimethylolpropane as an internal crosslinking agent was added to 4400 parts of a 37% by weight aqueous solution of sodium acrylate (75 mol% neutralization ratio) as a monomer component. 2.72 parts of triacrylate was dissolved to obtain a reaction solution. Next, the reaction solution was degassed for 30 minutes under a nitrogen gas atmosphere.
【0032】次いで、シグマ型羽根を2本有するジャケ
ット付きステンレス製双腕型ニーダーに蓋を付けた反応
器に上記反応液を供給し、反応液を30℃に保ちながら
上記反応器内を窒素ガス置換した。続いて、反応液を攪
拌しながら、重合開始剤としての過硫酸ナトリウム1.
1部、および重合開始剤の分解を促進する還元剤として
の亜硫酸ナトリウム1.1部を添加したところ、およそ
1分後に重合が開始した。そして、30℃〜80℃で重
合を行い、重合を開始して40分後に含水ゲル状重合体
を取り出した。Next, the reaction solution was supplied to a reactor equipped with a jacketed stainless steel double-armed kneader having two sigma-type blades, and the reaction solution was maintained at 30 ° C. and the inside of the reactor was filled with nitrogen gas. Replaced. Subsequently, while stirring the reaction solution, sodium persulfate as a polymerization initiator was added.
When 1 part and 1.1 parts of sodium sulfite as a reducing agent for accelerating the decomposition of the polymerization initiator were added, polymerization started about 1 minute later. Then, polymerization was carried out at 30 ° C. to 80 ° C., and the hydrogel polymer was taken out 40 minutes after the initiation of the polymerization.
【0033】得られた含水ゲル状重合体を金網上に広
げ、150℃で2時間熱風乾燥した。次いで、乾燥物を
ハンマーミルを用いて粉砕し、さらに30メッシュの金
網(目開き600μm)で分級することにより平均粒径
が220μmの不定型破砕状の吸水性樹脂(1)を得
た。次いで、上記の吸水性樹脂(1)100部に対し、
グリセリン0.5部、水2部およびイソプロピルアルコ
ール0.5部を含有する水性液をレディゲミキサー(M
5R、レディゲ社製)で約30分間混合し、得られた吸
水性樹脂混合物(1)を乾燥機の中に入れ220℃で2
時間の加熱処理をし、参考用吸水性樹脂(1)を得た。
参考用吸水性樹脂(1)の血液吸引量は12.4g/
g、含水率は0.5重量%であった。得られた参考用吸
水性樹脂(1)100部に水20部を滴下混合し、本発
明の吸液剤(1)を得た。 [実施例2]実施例1で得た参考用吸水性樹脂(1)1
00部に水50部を滴下混合し、本発明の吸液剤(2)
を得た。 [実施例3]実施例1で得た参考用吸水性樹脂(1)1
00部に水100部を滴下混合し、本発明の吸液剤
(3)を得た。 [実施例4]実施例1で得た参考用吸水性樹脂(1)1
00部に水200部を滴下混合し、本発明の吸液剤
(4)を得た。 [実施例5]実施例1で得た参考用吸水性樹脂(1)1
00部に水400部を滴下混合し、本発明の吸液剤
(5)を得た。 [実施例6]実施例1で得た参考用吸水性樹脂(1)1
00部に水900部を滴下混合し、本発明の吸液剤
(6)を得た。 [比較例1]実施例1で得た吸水性樹脂(1)100部
に対し、グリセリン0.5部、水2部およびイソプロピ
ルアルコール0.5部を含有する水性液をレディゲミキ
サー(M5R、レディゲ社製)で約30分間混合し、得
られた吸水性樹脂混合物(1)を乾燥機の中に入れ18
0℃で1時間の加熱処理をし、参考用吸水性樹脂(2)
を得た。参考用吸水性樹脂(2)の血液吸引量は2.6
g/g、含水率は1.3重量%であった。得られた参考
用吸水性樹脂(2)100部に水20部を滴下混合し、
比較用吸液剤(1)を得た。 [比較例2]比較例1で得た参考用吸水性樹脂(2)1
00部に水50部を滴下混合し、比較用吸液剤(2)を
得た。 [比較例3]比較例1で得た参考用吸水性樹脂(2)1
00部に水100部を滴下混合し、比較用吸液剤(3)
を得た。 [比較例4]比較例1で得た参考用吸水性樹脂(2)1
00部に水200部を滴下混合し、比較用吸液剤(4)
を得た。 [比較例5]比較例1で得た参考用吸水性樹脂(2)1
00部に水400部を滴下混合し、比較用吸液剤(5)
を得た。 [比較例6]比較例1で得た参考用吸水性樹脂(2)1
00部に水900部を滴下混合し、比較用吸液剤(6)
を得た。 [比較例7]実施例1で得た参考用吸水性樹脂(1)1
00部に水10部を滴下混合し、比較用吸液剤(7)を
得た。 [比較例8]実施例1で得た参考用吸水性樹脂(1)1
00部に水1900部を滴下混合し、比較用吸液剤
(8)を得た。The obtained hydrogel polymer was spread on a wire mesh and dried with hot air at 150 ° C. for 2 hours. Next, the dried product was pulverized using a hammer mill, and further classified with a 30-mesh wire mesh (mesh size: 600 μm) to obtain an irregularly crushed water-absorbent resin (1) having an average particle size of 220 μm. Next, with respect to 100 parts of the water absorbent resin (1),
An aqueous liquid containing 0.5 part of glycerin, 2 parts of water and 0.5 part of isopropyl alcohol was mixed with a Loedige mixer (M
5R, manufactured by Redige Co., Ltd.) for about 30 minutes, put the resulting water-absorbent resin mixture (1) in a dryer at 220 ° C. for 2 minutes.
Heat treatment was performed for a time to obtain a reference water-absorbent resin (1).
The blood suction amount of the reference water absorbent resin (1) is 12.4 g /
g, water content was 0.5% by weight. 20 parts of water was dropped and mixed with 100 parts of the obtained water-absorbing resin for reference (1) to obtain a liquid absorbing agent (1) of the present invention. Example 2 Reference water-absorbent resin (1) 1 obtained in Example 1
To 50 parts of water, 50 parts of water was dropped and mixed, and the liquid absorbing agent of the present invention (2)
I got [Example 3] Reference water-absorbent resin (1) 1 obtained in Example 1
100 parts of water and 100 parts of water were dropped and mixed to obtain a liquid absorbing agent (3) of the present invention. [Example 4] Reference water-absorbent resin (1) 1 obtained in Example 1
200 parts of water was dripped and mixed with 00 parts to obtain a liquid absorbing agent (4) of the present invention. [Example 5] The reference water-absorbent resin (1) 1 obtained in Example 1
400 parts of water was dropped and mixed with 00 parts to obtain a liquid absorbing agent (5) of the present invention. [Example 6] The reference water-absorbent resin (1) 1 obtained in Example 1
To 900 parts of water was added 900 parts of water dropwise to obtain a liquid absorbing agent (6) of the present invention. Comparative Example 1 An aqueous liquid containing 0.5 part of glycerin, 2 parts of water and 0.5 part of isopropyl alcohol was mixed with 100 parts of the water-absorbent resin (1) obtained in Example 1 using a Loedige mixer (M5R, And the resulting water-absorbent resin mixture (1) was placed in a dryer for 18 minutes.
Heat-treated at 0 ° C for 1 hour, and water-absorbent resin for reference (2)
I got The blood suction volume of the reference water absorbent resin (2) is 2.6.
g / g, and the water content was 1.3% by weight. 20 parts of water was dropped and mixed with 100 parts of the obtained reference water-absorbent resin (2),
A comparative liquid absorbing agent (1) was obtained. Comparative Example 2 Reference water-absorbent resin (2) 1 obtained in Comparative Example 1
To 50 parts of water, 50 parts of water were dropped and mixed to obtain a comparative liquid absorbing agent (2). Comparative Example 3 Reference water-absorbent resin (2) 1 obtained in Comparative Example 1
To 100 parts of water, 100 parts of water was dropped and mixed, and a comparative liquid absorbing agent (3)
I got [Comparative Example 4] Reference water-absorbent resin (2) 1 obtained in Comparative Example 1
200 parts of water were dropped and mixed with 00 parts, and a comparative liquid absorbing agent (4)
I got [Comparative Example 5] The reference water-absorbent resin (2) 1 obtained in Comparative Example 1
To 400 parts of water, 400 parts of water were dropped and mixed, and a comparative liquid absorbing agent (5)
I got Comparative Example 6 The reference water-absorbent resin (2) 1 obtained in Comparative Example 1
To 900 parts of water, 900 parts of water were dropped and mixed, and a comparative liquid absorbing agent (6)
I got [Comparative Example 7] Reference water-absorbent resin (1) 1 obtained in Example 1
To 10 parts of water, 10 parts of water was dropped and mixed to obtain a comparative liquid absorbing agent (7). [Comparative Example 8] Reference water-absorbent resin (1) 1 obtained in Example 1
1900 parts of water was dropped and mixed with 00 parts to obtain a comparative liquid absorbing agent (8).
【0034】上記で得られた参考用吸水性樹脂(1)、
吸液剤(1)〜(6)、参考用吸水性樹脂(2)、比較
用吸液剤(1)〜(8)について、血液吸収量と血液ゲ
ル吸収量を測定した。その結果を表1に示す。The reference water-absorbent resin (1) obtained above,
With respect to the liquid absorbing agents (1) to (6), the reference water absorbing resin (2), and the comparative liquid absorbing agents (1) to (8), the blood absorption amount and the blood gel absorption amount were measured. Table 1 shows the results.
【0035】[0035]
【表1】 [Table 1]
【0036】吸液剤(1)〜(6)は、いずれも血液吸
収量および血液ゲル吸収量が多い実用性に優れたもので
ある。一方、参考用吸水性樹脂(1)および(2)に示
されるように水を全く添加していないものは、血液吸収
量は多いが、血液ゲル吸収量が少ない。比較用吸液剤
(1)〜(6)は、参考用吸水性樹脂(2)の血液吸引
量が少なかったために、水を添加したところで血液ゲル
吸収性は改善されない。比較用吸液剤(7)では、水の
添加量が少ないためにその効果が見られず血液ゲル吸収
量は十分に向上していない。比較用吸液剤(8)では、
水の添加量が多く相対的な吸水性樹脂量が不足している
ため、血液吸収量の低下が見られ、また同様の理由から
水を添加した効果であるはずの血液ゲル吸収量の向上の
度合いも吸液剤(1)〜(6)と比べて低下する。 [実施例7]実施例1で得られた吸液剤(1)100部
と粉砕パルプ100部を乾式混合した後空気抄造し圧縮
して、密度0.15g/cc、坪量0.05g/cm2
の吸液性構造体を得た。次に、6cm×20cmに裁断
した上記吸液性構造体、液透過性ポリプロピレン製トッ
プシート、2枚のティッシュペーパー、レッグギャザー
およびウエストギャザーを含む液不透過性ポリエチレン
製バックシートおよび2つのテープファスナーからなる
吸収性物品(1)を両面テープにより個々のコンポーネ
ントを締結させ手で組み立てた。 [実施例8〜12、比較例9〜16]実施例7におい
て、吸液剤(1)に代えて吸液剤(2)〜(6)または
比較用吸液剤(1)〜(8)をそれぞれ用いた以外は実
施例7と同様にして、密度0.14〜0.17g/c
c、坪量0.047〜0.052g/cm2の範囲にあ
る吸液性構造体を得た。得られた吸液性構造体を用い、
実施例7と同様にして、本発明の吸収性物品(2)〜
(6)および比較用吸収性物品(1)〜(8)を組み立
てた。Each of the liquid absorbing agents (1) to (6) has a large amount of blood absorption and blood gel absorption and is excellent in practicality. On the other hand, as shown in the reference water-absorbing resins (1) and (2), those to which no water is added have a large blood absorption but a small blood gel absorption. In Comparative Liquid Absorbents (1) to (6), blood gel absorbability was not improved when water was added because the blood suction amount of Reference Water Absorbent Resin (2) was small. In Comparative Liquid Absorbent (7), the effect was not seen because the amount of water added was small, and the blood gel absorption was not sufficiently improved. In the comparative liquid absorbing agent (8),
Since the amount of water added is large and the relative water-absorbing resin amount is insufficient, a decrease in blood absorption is seen, and for the same reason, an increase in blood gel absorption, which should have been the effect of the addition of water. The degree also decreases as compared with the liquid absorbing agents (1) to (6). Example 7 100 parts of the liquid absorbing agent (1) obtained in Example 1 and 100 parts of pulverized pulp were dry-mixed, air-formed and compressed to a density of 0.15 g / cc and a basis weight of 0.05 g / cm. Two
Was obtained. Next, the liquid-absorbent structure cut into 6 cm × 20 cm, a liquid-permeable polypropylene topsheet, two tissue papers, a liquid-impermeable polyethylene backsheet including leg gathers and waist gathers, and two tape fasteners The absorbent component (1) consisting of was assembled by hand by fastening individual components with double-sided tape. [Examples 8 to 12 and Comparative Examples 9 to 16] In Example 7, liquid absorbing agents (2) to (6) or comparative liquid absorbing agents (1) to (8) were used instead of liquid absorbing agent (1). Except that the density was 0.14 to 0.17 g / c in the same manner as in Example 7.
c, a liquid-absorbing structure having a basis weight of 0.047 to 0.052 g / cm 2 was obtained. Using the obtained liquid absorbing structure,
In the same manner as in Example 7, the absorbent article (2) of the present invention
(6) and comparative absorbent articles (1) to (8) were assembled.
【0037】上記で得られた吸収性物品(1)〜(6)
および比較用吸収性物品(1)〜(8)について、血液
戻り量、を評価した。その結果を表2に示す。The absorbent articles (1) to (6) obtained above
The blood return amount of each of the comparative absorbent articles (1) to (8) was evaluated. Table 2 shows the results.
【0038】[0038]
【表2】 [Table 2]
【0039】[0039]
【発明の効果】本発明によると、血液吸収性および血液
ゲル吸収性に優れた吸液剤および吸収性物品を得ること
ができる。したがって、吸液剤または吸収性物品が血液
を二度以上に分けて少量ずつ吸収した場合にも、その合
計で十分に多くの血液を吸収することができる。According to the present invention, it is possible to obtain a liquid absorbing agent and an absorbent article having excellent blood absorbability and blood gel absorbability. Therefore, even when the liquid absorbing agent or the absorbent article divides blood into two or more portions and absorbs it little by little, it is possible to absorb a sufficiently large amount of blood in total.
Claims (8)
剤。1. A liquid absorbing agent having a blood gel absorption of 3 g / g or more.
と、該吸水性樹脂に対して20〜900重量%の水とを
含有する吸液剤。2. A liquid-absorbing agent containing a water-absorbing resin having a blood suction amount of 5 g / g or more, and 20 to 900% by weight of water based on the water-absorbing resin.
と、該吸水性樹脂に対して20〜900重量%の水とか
ら吸液剤を製造する方法。3. A method for producing a liquid absorbing agent from a water-absorbing resin having a blood suction amount of 5 g / g or more and 20 to 900% by weight of water based on the water-absorbing resin.
引量が5g/g以上の吸水性樹脂に水を加えて、含水率
15重量%以上とする吸液剤の製造方法。4. A method for producing a liquid-absorbing agent comprising adding water to a water-absorbent resin having a water content of less than 15% by weight and a blood suction amount of 5 g / g or more to make the water content 15% by weight or more.
と、該吸水性樹脂に対して20〜900重量%の水とを
含有する坪量20〜10000g/m2の吸収性物品。5. An absorbent article having a basis weight of 20 to 10,000 g / m 2 containing a water-absorbent resin having a blood suction amount of 5 g / g or more and water of 20 to 900% by weight based on the water-absorbent resin.
0〜10000g/m2で用いた吸収性物品。6. The liquid absorbent according to claim 1 or 2 having a basis weight of 2.
Absorbent article used in 0~10000g / m 2.
と、該吸水性樹脂に対して20〜900重量%の水とか
ら坪量20〜10000g/m2の吸収性物品を製造す
る方法。7. An absorbent article having a basis weight of 20 to 10000 g / m 2 is produced from a water-absorbing resin having a blood suction amount of 5 g / g or more and 20 to 900% by weight of water based on the water-absorbing resin. Method.
引量が5g/g以上の吸水性樹脂に水を加えて、含水率
15重量%以上とする、坪量20〜10000g/m2
の吸収性物品の製造方法。8. A water-absorbing resin having a water content of less than 15% by weight and a blood suction amount of 5 g / g or more is added with water to a water content of 15% by weight or more, and has a basis weight of 20 to 10,000 g / m 2.
Method for producing an absorbent article.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20944497A JP3145334B2 (en) | 1997-08-04 | 1997-08-04 | Liquid-absorbing agent, absorbent article, and method for producing them |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20944497A JP3145334B2 (en) | 1997-08-04 | 1997-08-04 | Liquid-absorbing agent, absorbent article, and method for producing them |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH1147588A true JPH1147588A (en) | 1999-02-23 |
| JP3145334B2 JP3145334B2 (en) | 2001-03-12 |
Family
ID=16572972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20944497A Expired - Fee Related JP3145334B2 (en) | 1997-08-04 | 1997-08-04 | Liquid-absorbing agent, absorbent article, and method for producing them |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3145334B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012170875A (en) * | 2011-02-21 | 2012-09-10 | Nac Feeding Kk | Butterfat treating agent |
-
1997
- 1997-08-04 JP JP20944497A patent/JP3145334B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012170875A (en) * | 2011-02-21 | 2012-09-10 | Nac Feeding Kk | Butterfat treating agent |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3145334B2 (en) | 2001-03-12 |
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