JPH04208162A - Portable bag for gatthering urine and ostomy bag - Google Patents
Portable bag for gatthering urine and ostomy bagInfo
- Publication number
- JPH04208162A JPH04208162A JP2340565A JP34056590A JPH04208162A JP H04208162 A JPH04208162 A JP H04208162A JP 2340565 A JP2340565 A JP 2340565A JP 34056590 A JP34056590 A JP 34056590A JP H04208162 A JPH04208162 A JP H04208162A
- Authority
- JP
- Japan
- Prior art keywords
- water
- bag
- polyvinyl alcohol
- film
- coated
- 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
- 210000002700 urine Anatomy 0.000 title claims abstract description 17
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 39
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 39
- 239000005871 repellent Substances 0.000 claims abstract description 30
- 238000007127 saponification reaction Methods 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 58
- 230000002940 repellent Effects 0.000 claims description 24
- 239000003349 gelling agent Substances 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 abstract description 6
- 239000002699 waste material Substances 0.000 abstract description 5
- 238000001879 gelation Methods 0.000 abstract description 3
- 210000000436 anus Anatomy 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000126 substance Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 230000002745 absorbent Effects 0.000 description 4
- 239000002250 absorbent Substances 0.000 description 4
- 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 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 229920000247 superabsorbent polymer Polymers 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920002689 polyvinyl acetate Polymers 0.000 description 3
- 239000011118 polyvinyl acetate Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- QLOKJRIVRGCVIM-UHFFFAOYSA-N 1-[(4-methylsulfanylphenyl)methyl]piperazine Chemical compound C1=CC(SC)=CC=C1CN1CCNCC1 QLOKJRIVRGCVIM-UHFFFAOYSA-N 0.000 description 1
- PGYZAKRTYUHXRA-UHFFFAOYSA-N 2,10-dinitro-12h-[1,4]benzothiazino[3,2-b]phenothiazin-3-one Chemical compound S1C2=CC(=O)C([N+]([O-])=O)=CC2=NC2=C1C=C1SC3=CC=C([N+](=O)[O-])C=C3NC1=C2 PGYZAKRTYUHXRA-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- JFGQHAHJWJBOPD-UHFFFAOYSA-N 3-hydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)NC1=CC=CC=C1 JFGQHAHJWJBOPD-UHFFFAOYSA-N 0.000 description 1
- LHYQAEFVHIZFLR-UHFFFAOYSA-L 4-(4-diazonio-3-methoxyphenyl)-2-methoxybenzenediazonium;dichloride Chemical compound [Cl-].[Cl-].C1=C([N+]#N)C(OC)=CC(C=2C=C(OC)C([N+]#N)=CC=2)=C1 LHYQAEFVHIZFLR-UHFFFAOYSA-L 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000012544 Viola sororia Nutrition 0.000 description 1
- 244000172533 Viola sororia Species 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- SUXCALIDMIIJCK-UHFFFAOYSA-L disodium;4-amino-3-[[4-[4-[(1-amino-4-sulfonatonaphthalen-2-yl)diazenyl]-3-methylphenyl]-2-methylphenyl]diazenyl]naphthalene-1-sulfonate Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(N=NC3=CC=C(C=C3C)C=3C=C(C(=CC=3)N=NC=3C(=C4C=CC=CC4=C(C=3)S([O-])(=O)=O)N)C)=CC(S([O-])(=O)=O)=C21 SUXCALIDMIIJCK-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 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
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000004335 litholrubine BK Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000002906 medical waste Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- JHOKTNSTUVKGJC-UHFFFAOYSA-N n-(hydroxymethyl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCO JHOKTNSTUVKGJC-UHFFFAOYSA-N 0.000 description 1
- MEMUMYCLWQPAEX-UHFFFAOYSA-N n-octadecylaziridine-1-carboxamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)N1CC1 MEMUMYCLWQPAEX-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- ZODDGFAZWTZOSI-UHFFFAOYSA-N nitric acid;sulfuric acid Chemical compound O[N+]([O-])=O.OS(O)(=O)=O ZODDGFAZWTZOSI-UHFFFAOYSA-N 0.000 description 1
- VRQWWCJWSIOWHG-UHFFFAOYSA-J octadecanoate;zirconium(4+) Chemical compound [Zr+4].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O VRQWWCJWSIOWHG-UHFFFAOYSA-J 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- ZFMRLFXUPVQYAU-UHFFFAOYSA-N sodium 5-[[4-[4-[(7-amino-1-hydroxy-3-sulfonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazenyl]-2-hydroxybenzoic acid Chemical compound C1=CC(=CC=C1C2=CC=C(C=C2)N=NC3=C(C=C4C=CC(=CC4=C3O)N)S(=O)(=O)O)N=NC5=CC(=C(C=C5)O)C(=O)O.[Na+] ZFMRLFXUPVQYAU-UHFFFAOYSA-N 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- UAWGEYZZCKAPHY-XBFRWELRSA-N sodium;5-[(4-ethoxyphenyl)diazenyl]-2-[(e)-2-[4-[(4-ethoxyphenyl)diazenyl]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound [Na+].C1=CC(OCC)=CC=C1N=NC(C=C1S(O)(=O)=O)=CC=C1\C=C\C1=CC=C(N=NC=2C=CC(OCC)=CC=2)C=C1S(O)(=O)=O UAWGEYZZCKAPHY-XBFRWELRSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- OLSOUGWNONTDCK-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=CC4=CC(=CC(N)=C4C=3O)S([O-])(=O)=O)S([O-])(=O)=O)OC)=C(O)C2=C1N OLSOUGWNONTDCK-UHFFFAOYSA-J 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業−1−の利用分野)
本発明は、携帯用採尿バッグ及びオストミ−バッグに関
するものであり、さらに詳しくは使用時には尿1人工肛
門等からの排出lη物などを漏らすことなく確実に溜め
ることができ、廃棄時には水洗トイレ等にバッグごと捨
てることができるバッグに関するものである。Detailed Description of the Invention (Field of Application of Industry-1-) The present invention relates to a portable urine collection bag and an ostomy bag, and more specifically, the present invention relates to a portable urine collection bag and ostomy bag. The present invention relates to a bag that can be reliably filled with water without leaking, and that can be thrown away together with the bag in a flush toilet or the like when discarded.
(従来の技術)
現在、市販されている携帯用採尿バッグなどの汚物袋の
多くは排泄された水分を含んだ汚物を高吸収ポリマー等
によって固形化し、水分不透過性累月からなる袋内に固
形化した汚物を保持するものである。そして、その廃棄
方法は使用済の汚物袋を固形化した汚物ごと一般ゴミと
して捨てるか。(Prior art) Most of the filth bags currently on the market, such as portable urine collection bags, solidify excreted water-containing filth with a superabsorbent polymer, etc., and store it in a bag made of water-impermeable material. It holds solidified filth. As for how to dispose of it, should you throw away the used waste bag along with the solidified waste as general garbage?
もしくは、固形化した汚物だ&Jをトイレに投棄し。Or, dump the &J, which is solidified filth, into the toilet.
汚物袋は一般のゴミとして捨てる方法により処理されて
いる。Garbage bags are disposed of by being disposed of as regular garbage.
また、オス1ミーバツグについては、従来のオストミ−
バッグは、低密度ポリエチレン、軟質ポリ塩化ビニル等
の水に溶解もしくは分散しないフィルムが使用されてい
る。そして、使用済のオス)・ミーバッグは、毎日、−
週間等の周期で収集されるゴミとして処理されている。In addition, regarding the male 1 me bag, the conventional ostomy
The bags are made of films such as low-density polyethylene and soft polyvinyl chloride that do not dissolve or disperse in water. And the used male) me bag is -
It is treated as garbage that is collected on a weekly basis.
例えば、特開昭63−181758号公報にはラミネー
1の一層が温水可溶性と耐久性テッシュベーバーからな
る流水に投棄可能な人工肛門用バうヂが記載されている
が、トイレの水には分散せず、トイレの機能に悪影響を
及ぼしている。For example, Japanese Patent Application Laid-Open No. 63-181758 describes a colostomy budge that can be disposed of in running water, and one layer of laminate 1 is made of hot water-soluble and durable tissue material. It is not dispersing and has a negative impact on the functioning of the toilet.
(発明が解決しようとする課題)
上記のような現在市販されている携帯用採尿ハック、オ
ス1−ミーバッグ等の汚物袋は、汚物の保持性及び防漏
性には優れているが、防漏材として水には不溶性の材料
1例えばポリエチレン等のポリマーが使用されているた
め、水洗トイレへ投棄した場合には排水設備に悪影響を
及ぼすことが予想され1袋ごと水洗1− (レヘ投棄で
きず、その処理が煩わし7いという問題かあ、った。(Problems to be Solved by the Invention) The currently commercially available filth bags such as the portable urine collection hack and the male 1-me bag described above are excellent in retaining filth and leak-proofing, but are not leak-proof. Since the materials used are polymers such as polyethylene, which are insoluble in water, it is expected that if they are disposed of in a flush toilet, it will have a negative effect on the drainage system. The problem was that the process was cumbersome.
本発明は、比較的長い時間汚物を保持することができ、
さらに水洗トイレに廃棄することができる携帯用採尿バ
ッグ及びオス1〜ミーバツグを提供するごとを目的とす
る。The present invention can hold waste for a relatively long time,
Another object of the present invention is to provide a portable urine collection bag and a male to me bag that can be disposed of in a flush toilet.
(課題を解決するための手段)
本発明者らは、−1、記のごとき目的を達成すべく鋭意
研究を重ねたところ、ポリビニルアルコールのゲルの生
成機構並びに撥水剤のもつ水をはじく機能を組み合わせ
ることにより、飛躍的にフィルムの片面の水不透過性を
高め、かつフィルムを水中に投棄した際には短時間で水
に溶解もしくは分散することができ、携帯用採尿バッグ
及びオストミ−バッグとして有用であることを見出し2
本発明に到達したものである。(Means for Solving the Problems) The inventors of the present invention have conducted extensive research to achieve the following objectives: -1.The inventors have discovered the gel formation mechanism of polyvinyl alcohol and the water repelling function of water repellent agents. By combining these, the water impermeability of one side of the film is dramatically increased, and when the film is disposed of in water, it can be dissolved or dispersed in water in a short time, making it suitable for portable urine collection bags and ostomy bags. Headline 2 found to be useful as
This has led to the present invention.
ずなわら2本発明は次の点を要旨とするものである。Zunawara 2 The gist of the present invention is as follows.
(1)ケン化度が70〜98%のポリビニルアルコール
とポリビニルアルコールのゲル化促進剤とからなるフィ
ルJ、の片面に撥水剤がコーティングされたフィルムか
らなり、撥水剤がコーティングされた面が内側となるよ
うに成形された携帯用採尿バッグ。(1) A film J made of polyvinyl alcohol with a degree of saponification of 70 to 98% and a polyvinyl alcohol gelling promoter, and one side of which is coated with a water repellent; the surface coated with the water repellent. A portable urine collection bag that is shaped so that the inside is inside.
(2)ケン化度が70〜98%のポリビニルアルコール
とポリビニルアルニl−ルのゲル化促進剤とからなるフ
ィルムの片面に撥水剤がコーティングされたフィルムか
らなり、撥水剤がコーティングされた面が内側となるよ
うに成形されたオス1−ミーバッグ。(2) A film made of polyvinyl alcohol with a degree of saponification of 70 to 98% and a gelling promoter of polyvinylalnyl, one side of which is coated with a water repellent; A male 1-me bag shaped so that the side faces inside.
以下2本発明の詳細な説明する。Two aspects of the present invention will be described in detail below.
マス、ポリビニルアルコールとは、ポリビニルアルコー
ルまたはその誘導体をいう。ポリビニルアルコールは、
酢酸ビニルを重合させたポリ酢酸ビニルを加水分解、す
なわち脱酢酸させて製造する等、公知の方法によって1
階られる。この工程の中で、加水分解の程度がケン化度
と呼ばれ、ケン化度はポリビニルアルコールのモノマー
ユニットのうち、いくら脱酢酸されているのか、その割
合を表す尾である。たとえば、ケン化度100%とは、
ポリ酢酸ビニルの酢酸エステル残基がすべて水酸基に加
水分解されていることをいい、ケン化度95%のポリビ
ニルアルコールとは、ポリ酢酸ビニルのモノマーユニッ
トが95%水酸基に置換されたものを意味する。Mass, polyvinyl alcohol refers to polyvinyl alcohol or a derivative thereof. Polyvinyl alcohol is
1 by a known method such as producing polyvinyl acetate by polymerizing vinyl acetate, that is, by deaceticating it.
I am floored. In this process, the degree of hydrolysis is called the degree of saponification, and the degree of saponification is a measure of how many of the monomer units of polyvinyl alcohol have been deacetated. For example, a degree of saponification of 100% means
It means that all the acetate residues of polyvinyl acetate have been hydrolyzed to hydroxyl groups, and polyvinyl alcohol with a degree of saponification of 95% means polyvinyl acetate in which 95% of the monomer units have been substituted with hydroxyl groups. .
本発明で用いられるポリビニルアルコールは。The polyvinyl alcohol used in the present invention is.
ケン化度が70〜98%であり、このポリビニルアルコ
ールは約40°C以下の水に溶解もしくは膨潤又は分散
するものであればよく、特に制限6才ない。また、ポリ
ビニルアルコールの分子量、すなわち重合度に制限はな
く2例えば、低重合度と高重合度のポリビニルアルコー
ルをブレンドして使うことも可能である。さらに、約4
0°C以下の水に溶解もしくは膨潤あるいは分散するの
であるなら、酢酸ビニルと共重合させることが可能なモ
ノマーをポリビニルアルニl−ルのモノマーとして含む
二元、三元もしくは四元共重合体であっても構わない。The degree of saponification is 70 to 98%, and the polyvinyl alcohol is not particularly limited to 6 years as long as it dissolves, swells, or disperses in water at a temperature of about 40° C. or less. Furthermore, there is no limit to the molecular weight of polyvinyl alcohol, that is, the degree of polymerization; for example, it is also possible to use a blend of polyvinyl alcohol with a low degree of polymerization and a polyvinyl alcohol with a high degree of polymerization. Furthermore, about 4
If it dissolves, swells, or disperses in water at temperatures below 0°C, it is a binary, ternary, or quaternary copolymer containing a monomer that can be copolymerized with vinyl acetate as a polyvinylalnylene monomer. It doesn't matter if there is.
共重合可能なモノマー成分としては1分子中に二重結合
を有する千ツマ−が挙げられる。Examples of monomer components that can be copolymerized include 1,000 polymers having a double bond in one molecule.
−例を挙げるなら、メチルビニルエーラール、スチレン
、塩化ビニル、アリルアルコール、アクリル酸およびそ
のエステル、ツタクリル酸およびそのエステル、アクリ
ロニトリル、ビニルピロリドン。- Methylvinyleral, styrene, vinyl chloride, allyl alcohol, acrylic acid and its esters, tutaacrylic acid and its esters, acrylonitrile, vinylpyrrolidone, to name a few.
クロロプレン、ブタジェン、イソプレン、エチレン、プ
ロピレン等が挙げられる。Examples include chloroprene, butadiene, isoprene, ethylene, propylene, and the like.
本発明で用いられるポリビニルアルコールのゲル化促進
剤とは、ポリビニルアルコールに対して凝析効果を有す
る塩類やポリビニルアルコールとジオール型の化学結合
等が可能である物質等をいう。本発明に好まし2く用い
られる塩類としては。The polyvinyl alcohol gelation promoter used in the present invention refers to salts that have a coagulating effect on polyvinyl alcohol, substances that can form diol-type chemical bonds with polyvinyl alcohol, and the like. The salts preferably used in the present invention include:
硫酸すトリウム、′6N酸マグネシウム、硫酸アルミニ
ウム、硫酸アンモニウム、硫酸カリウム等の硫酸塩、硝
酸すトリウム、硝酸アンモニウJ1.硝酸アルミニウム
等の硝酸塩、リン酸ナトリウム等のリン酸塩、クロム酸
カリウJ・等のクロム酸塩等が挙げられる。また、ポリ
ビニルアルコールと上記化学結合が可能な物質としては
、硼酸、硼酸塩。Sulfates such as sodium sulfate, magnesium '6N acid, aluminum sulfate, ammonium sulfate, potassium sulfate, sulfuric acid nitrate, ammonium nitrate J1. Examples include nitrates such as aluminum nitrate, phosphates such as sodium phosphate, and chromates such as potassium chromate J. In addition, substances that can form the above chemical bond with polyvinyl alcohol include boric acid and borates.
硼砂や銅、アルミニウム、チタン、ジルコニウム。Borax, copper, aluminum, titanium, zirconium.
スズ、バナジウム等の化合物が挙げられる。Examples include compounds such as tin and vanadium.
これらのゲル化促進剤のポリビニルアルコールに対する
割合は、ポリビニルアルコールのモノマーユニットに対
して、各ゲル化促進剤のゲル化能力によって異なるが、
0.1〜30モル%、好ましくは0.1〜20モル%含
んでいるものがよい。ゲル化剤濃度が0.1モル%より
低いと、フィルムに要求されろ水不透過性能が悪くなり
、また、30モル%を超えると、逆にフィルムの水溶性
が十分に得られず、目的とするフィルム性能が得られな
い。The ratio of these gelling promoters to polyvinyl alcohol varies depending on the gelling ability of each gelling promoter to the monomer unit of polyvinyl alcohol.
The content is preferably 0.1 to 30 mol%, preferably 0.1 to 20 mol%. If the gelling agent concentration is lower than 0.1 mol%, the water impermeability required of the film will be poor, and if it exceeds 30 mol%, the film will not have sufficient water solubility, and the desired The desired film performance cannot be obtained.
本発明におけるゲル化剤とポリビニルアルコールを構成
要素とするフィルムは、いろいろな方法で製造すること
が可能である。好ましくは、ポリビニルアルコールは、
公知の方法により、適当な温度の水に溶解、膨潤もしく
は分散させた後、ゲル化促進剤の水溶液もしくは分散液
を加え、1%!拌下に混合し、流延、乾燥という工程を
経て製造できる。フィルム強度を増大させるために、熱
処理工程を加えても構わない。The film containing the gelling agent and polyvinyl alcohol in the present invention can be produced by various methods. Preferably, the polyvinyl alcohol is
After dissolving, swelling or dispersing in water at an appropriate temperature by a known method, an aqueous solution or dispersion of a gelling accelerator is added, and the gelation promoter is dissolved, swollen or dispersed in water at an appropriate temperature. It can be manufactured through the steps of mixing with stirring, casting, and drying. A heat treatment step may be added to increase the film strength.
本発明で用いられるフィルムは、以」−のような条件で
得られたゲル化促進剤を含有したポリビニルアルコール
フィルl、の片面に、撥水剤をコーティング法、スプレ
ー法等の公知の方法にて:1−ティングすることにより
得られる。The film used in the present invention is obtained by applying a water repellent to one side of a polyvinyl alcohol film containing a gelling promoter obtained under the following conditions using a known method such as coating or spraying. Te: Obtained by 1-ting.
一般に撥水剤とは、フィルム表面に水による湿潤(ぬれ
)に抵抗する性能を付5゜することを撥水加工といい、
これに使用する薬剤のことをいう。In general, water repellent agents are called water repellent finishing, which means adding properties to the film surface to resist wetting (wetting) by water.
Refers to the drug used for this purpose.
撥水剤は、繊維製品、特に織物等の表面加工に一般に使
用されている。表面に撥水性を与えるには。Water repellents are commonly used for surface treatment of textile products, especially textiles. To make the surface water repellent.
水をはじく物質が必要であり2表面エネルギーの小さい
化合物はど水をはじきゃすい傾向にある。A substance that repels water is required, and compounds with low surface energy tend to repel water.
化学構造で示せば、−CF3〉−CF2〉−C14゜>
−CH□の順に水をよくはじく。すなわち、パラフィン
やステアリン酸等の飽和炭化水素部分のある化合物やシ
リコーン樹脂のように多数のメチル基をもつ化合物が、
一般に撥水性を与える部分として知られている。さらに
、ペルフルオロアルキル基をもつフッ素化合物は、撥水
性と油性物質をはじく撥油性も兼ね備えている。In terms of chemical structure, -CF3〉-CF2〉-C14゜〜
Repel water well in the order of -CH□. In other words, compounds with saturated hydrocarbon moieties such as paraffin and stearic acid, and compounds with many methyl groups such as silicone resins,
It is generally known as a part that provides water repellency. Furthermore, fluorine compounds with perfluoroalkyl groups have both water-repellent properties and oil-repellent properties that repel oily substances.
本発明で用いられる撥水剤として代表的な化合物を例示
すると、パラフィン、ステアリン酸アルミニウム、ステ
アリン酸ジルコニウム、シリコーン樹脂またはメチルヒ
ドロポリシロキサンを主成分とし、触媒により網状化す
る反応性シリコーン化合物やピリジニウム塩型陽イオン
界面活性剤。Typical water repellent compounds used in the present invention include paraffin, aluminum stearate, zirconium stearate, silicone resin or methylhydropolysiloxane as a main component, and reactive silicone compounds that form a network with a catalyst and pyridinium Salt-type cationic surfactant.
メチロールステアラミド、オクタデシルエチレンウレア
等の反応性を有する長鎖の飽和炭化水素系化合物、さら
には、ペルフルオロアルキル基を側=8−
鎖にもつアクリル酸ポリフルオロアルキルエステルを構
成単位として含有する化合物やフッ素を主鎖に含む化合
物が挙げられる。水、さらには油をはしく性質を有する
ペルフルオロアルキル基をもつ化合物を成分とする撥水
剤が好ましく用いられるが、用途に応じて他の撥水剤を
選んでも構わない。また、コーテイング量並びにコーテ
イング後の加熱処理方法に制限はない。Reactive long-chain saturated hydrocarbon compounds such as methylol stearamide and octadecyl ethylene urea, as well as compounds containing acrylic acid polyfluoroalkyl esters having a perfluoroalkyl group on the side = 8-chain as a constituent unit; Examples include compounds containing fluorine in the main chain. A water repellent containing a compound having a perfluoroalkyl group that repels water and even oil is preferably used, but other water repellents may be selected depending on the application. Moreover, there are no restrictions on the amount of coating and the method of heat treatment after coating.
上記のような↑發水剤は、1發水性をもつ化合物を少量
の界面活性剤を用いて水中に乳化した状態のものあるい
は溶媒中に分散・溶解したものをフィルム表面にコーテ
ィング法等の公知の方法でコーティングすることができ
、用途に応じて乾燥、熱処理を施せばよい。The above-mentioned ↑water-retaining agents are produced by coating the surface of a film with a water-retaining compound emulsified in water using a small amount of surfactant, or dispersed/dissolved in a solvent. It can be coated using the following methods, and may be dried and heat treated depending on the application.
本発明のフィルムの厚みは特に制限はないが。The thickness of the film of the present invention is not particularly limited.
通常25〜250μmの厚みが好ましく使用される。Usually, a thickness of 25 to 250 μm is preferably used.
また、フィルムの柔軟性をよくするために、フィルムの
性能を損なわない程度に可塑剤を添加してもよい。可塑
剤としては、−・般にグリコール類が用いられる。例え
ば、エチレングリコール、トリメチレングリコール、テ
トラメチレングリコール、ペンタメチレングリ:1−ル
、ヘキザメチビジグリコール、プロピレングリコール、
グリセリン。Further, in order to improve the flexibility of the film, a plasticizer may be added to an extent that does not impair the performance of the film. As the plasticizer, glycols are generally used. For example, ethylene glycol, trimethylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, propylene glycol,
Glycerin.
2.3−ブタンジオール、1,3−ブタンジオール。2.3-butanediol, 1,3-butanediol.
ジエヂビジグリコール、トリエチl/ングリコール等が
挙げられる。Examples include diezibidiglycol, triethyl/glycol, and the like.
さらに、ポリビニルアルコールを主成分とするフィルム
層に着色を施すため、フィルムの性能および強度を損な
わない程度に着色剤もしくは染料を添加しても構わない
。例えば、ベンゾプルプリン4 B K X (Ben
zopurpurine4 B K X ) 、 ニラ
ポンオレンジG C(Nippon Orange G
C) 、 クリソフェニンN S (Chryso
phenine N S ) 、ダイレフ1−スカイブ
ルー5 B (Direct Sky Blue 5
B ) 。Furthermore, in order to color the film layer containing polyvinyl alcohol as a main component, a colorant or dye may be added to an extent that does not impair the performance and strength of the film. For example, benzopurpurin 4 B K
zopurpurine4 B K
C), chrysofenine NS (Chryso
phenine NS), Direct Sky Blue 5
B).
ニラポンファーストバイオレットB B (Nippo
nFast Vio−let B B ) 、 ダイレ
クトブラウンM(Direct Brown M)
、 ニラポンディープブラックエキストう(Nippo
n Deep Black extra ) 、ザルフ
ァーインディゴR(Sulphur Indigo
R) 。Nippo First Violet B B (Nippo
nFast Vio-let B B ), Direct Brown M
, Nippo Deep Black Extract
n Deep Black extra), Sulfur Indigo R
R).
ザルファーブラックB C(Sulphur Blac
k B C) 。Sulfur Black B C
k B C).
ミゲスレンブルーR8(旧kethrene Blue
RS ) 。Migesrene Blue R8 (formerly Kethrene Blue
RS).
ナフト−ルAS (Naphtol AS) 、ファー
ス1−スカーレットGヘース(Fast 5carle
t G Ba5e ) 。Naphtol AS, Fast 5carle
tGBa5e).
ロゼリンNS (Rocceline NS) 、 ア
シッドブリリアントスカーレット3 R(Acid B
r1lliantScarlet 3 R)、クロムグ
リーンF (Chrome GreenF)、クロムブ
ラックA C(ChromeB]ack A C) 。Rocceline NS, Acid Brilliant Scarlet 3 R (Acid B
r1lliantScarlet 3 R), Chrome Green F, Chrome Black A C (Chrome B]ack A C).
ロダミンB (Rhodamine B ) 、 セリ
トンファース1−ピンクF 3 B (Cellito
n Fast PinkF 3 B ) 。Rhodamine B, Cellito Firth 1-Pink F3 B (Cellito
nFast PinkF3B).
セリトンファースI−ブルーF F R(Cellit
on FastBlue F F R)等が挙げられ
る。Celliton Firth I-Blue F F R (Cellit
on FastBlue F F R), etc.
上記のようにして得たフィル1、から本発明の携帯用採
尿バッグ又はオス1−ミーバッグを得るには。To obtain the portable urine collection bag or male 1-me bag of the present invention from the fill 1 obtained as described above.
フィルムを溶剤もしくは接着剤による接着法、ヒートシ
ール法、インパルスシール法、超音波接合法等の接合法
等の公知の方法を用いて成形する。The film is formed using a known method such as a bonding method using a solvent or adhesive, a bonding method such as a heat sealing method, an impulse sealing method, or an ultrasonic bonding method.
本発明においては、バッグを形成するフィルムと吸収保
持材をkJl ;’を合わせてバッグを形成することも
できる。In the present invention, the bag can also be formed by combining the bag-forming film and the absorption/retention material in kJl;'.
−11〜
吸収保持材としては、吸水紙、水分散性の織布もしくは
不織布上に高吸収性ポリマーの粒状物もしくは粉末を均
一に散布したもの、あるいは粉砕パルプなどの吸収剤の
間に上記高吸収ポリマーを混合したものを配置して薄い
層を形成させ、さらにその」二面を高含水率性能を有す
る吸水紙、水分散性織布あるいは不織布で被覆して固定
したものが挙げられる。さらに、使用時に排泄された尿
の水分によって溶解するような素材2例えば、水溶性の
ポリビニルアルコールフィルムからなる小袋の中に高分
子吸収剤を収納したものなどがあげられる。-11~ The absorbent and retaining material may be water-absorbing paper, water-dispersible woven or non-woven fabric with granules or powder of a superabsorbent polymer uniformly dispersed, or the above-mentioned superabsorbent polymer between absorbents such as pulverized pulp. An example is one in which a mixture of absorbent polymers is arranged to form a thin layer, and its two sides are further covered and fixed with water-absorbing paper, water-dispersible woven fabric, or non-woven fabric with high water content performance. Furthermore, a material 2 that dissolves in the water of urine excreted during use may include, for example, a pouch made of water-soluble polyvinyl alcohol film containing a polymer absorbent.
」1−記の高吸収性ポリマーとしては、澱粉類、架橋も
しくは加工澱粉、澱粉−アクリル酸系モノマーグラフ1
〜物、カルボキシメチルセルロースおよびその誘導体、
親水性アクリル酸もしくはメタクリル酸共重合体、高分
子量ポリエチレンオキザサイドとその架橋物、ポリビニ
ルアルコールとその誘導体等の群から選ばれる一種また
は二種以上の混合物であって水と接触した場合、ポリマ
ーの重量にたいして50〜1ooo倍の多量の水を吸収
しゲル化する性質を有するものである。これらのポリマ
ーは水に対して不溶性のものであるが1粒状もしくは粉
末状で吸収保持層に配置されているため水分散性を有し
、水洗トイレに投棄しても問題はない。Examples of the superabsorbent polymer described in 1-1 include starches, crosslinked or modified starches, and starch-acrylic acid monomer graph 1.
~ substances, carboxymethyl cellulose and its derivatives,
One or a mixture of two or more selected from the group of hydrophilic acrylic acid or methacrylic acid copolymers, high molecular weight polyethylene oxide and its crosslinked products, polyvinyl alcohol and its derivatives, etc. When in contact with water, the polymer It has the property of absorbing 50 to 100 times as much water as its weight and turning it into a gel. Although these polymers are insoluble in water, they are dispersible in water because they are arranged in the absorption and retention layer in the form of single particles or powder, so there is no problem even if they are disposed of in a flush toilet.
本発明におけるケン化度が70〜98%のポリビニルア
ルコールとポリビニルアルコールのゲル化促進剤とから
なるフィルムの片面に撥水剤がコーティングされたフィ
ルムからなり、撥水剤がコーティングされた面が内側と
なるように成形されたバッグは、携帯用採尿バッグ、オ
ストミ−バッグのほか、医療廃棄物用容器、ランドリー
バッグ。In the present invention, the film is made of polyvinyl alcohol with a degree of saponification of 70 to 98% and a polyvinyl alcohol gelling promoter, and one side of the film is coated with a water repellent, and the surface coated with the water repellent is on the inside. Bags shaped to be used include portable urine collection bags, ostomy bags, medical waste containers, and laundry bags.
生ゴミ処理バッグ等としても利用できる。It can also be used as a garbage disposal bag, etc.
(実施例) 以下9本発明を実施例によって具体的にに説明する。(Example) EXAMPLES The present invention will be specifically explained below using examples.
実施例1
ポリビニルアルコール(以下、PVAと略t。)(UF
−170M、ユニチカ■製、ゲン化度95゜5〜97.
5モル%)を15gビーカーに採り、蒸留水90gを加
えて十分に膨潤させた後、90°Cの湯浴中で強攪拌下
にPVAを溶解した。この溶液に硫酸アルミニウムi、
i 7 gを蒸留水10gに溶解したものを攪拌下に
加え、混合した。溶液中の気泡を脱泡した後、混合液を
ポリエチレンテレフタレートフィルム」二に流延し、室
温で一晩風乾した。得られたフィルムをAフィルムとす
る。Example 1 Polyvinyl alcohol (hereinafter abbreviated as PVA) (UF
-170M, manufactured by Unitika ■, degree of genification 95°5-97.
5 mol %) was placed in a beaker, 90 g of distilled water was added to sufficiently swell it, and then PVA was dissolved in a 90°C hot water bath with strong stirring. In this solution, aluminum sulfate i,
A solution of 7 g of i in 10 g of distilled water was added under stirring and mixed. After defoaming the air bubbles in the solution, the mixed solution was cast onto a polyethylene terephthalate film and air-dried overnight at room temperature. The obtained film is referred to as A film.
次に、20cm角のAフィルムに撥水剤としてAG−6
50(旭硝子■製)を約2 ml均一に塗布した後、室
温で約1時間乾燥し、さらに100°Cで約10分の加
熱処理を施した。Next, AG-6 was applied as a water repellent to a 20 cm square A film.
After about 2 ml of 50 (manufactured by Asahi Glass ■) was evenly applied, it was dried at room temperature for about 1 hour, and then heated at 100°C for about 10 minutes.
比較例1
実施例1において、撥水剤を塗布せずに100°Cで約
10分の加熱処理を行った以外は、同様の操作を施した
。Comparative Example 1 The same operation as in Example 1 was performed except that a heat treatment was performed at 100° C. for about 10 minutes without applying a water repellent.
実施例2
実施例1において、硫酸アルミニウム1.17 gを硼
酸0.21gに代えた以外は、同様の操作を行った。Example 2 The same operation as in Example 1 was performed except that 1.17 g of aluminum sulfate was replaced with 0.21 g of boric acid.
比較例2
実施例2において、撥水剤を塗布せずに100°Cで約
10分の加熱処理を行った以外は、同様の操作を施した
。Comparative Example 2 The same operation as in Example 2 was performed except that a heat treatment was performed at 100° C. for about 10 minutes without applying a water repellent.
実施例3
実施例1において、PVA (UF−170M)をPV
A(UP−180)(ユニチカ■製、ゲン化度87〜8
9モル%)に代えた以外は、同様の操作を行った。Example 3 In Example 1, PVA (UF-170M) was
A (UP-180) (manufactured by Unitika ■, degree of genification 87-8
The same operation was performed except that the concentration was changed to 9 mol %).
比較例3
実施例3において、撥水剤を塗布せずに100°Cで約
10分の加熱処理を行った以外は、同様の操作を行った
。Comparative Example 3 The same operation as in Example 3 was performed except that a heat treatment was performed at 100° C. for about 10 minutes without applying a water repellent.
実施例4
実施例3において、硫酸アルミニウム1.17gを硼酸
0.21gに代えた以外は、同様の操作を行った。Example 4 The same operation as in Example 3 was performed except that 1.17 g of aluminum sulfate was replaced with 0.21 g of boric acid.
比較例4
実施例4において、撥水剤を塗布せず乙こ100°Cで
約10分の熱処理を加えた以り(は、同様の操作を行っ
た。Comparative Example 4 The same operation as in Example 4 was performed except that no water repellent was applied and heat treatment was applied at 100°C for about 10 minutes.
実施例5
実施例1において、PVA(UF−170M)をP V
A (E−180) (:’−ニチhQ@製、ケン
化度87〜89モル%)に代えた以外は、同様の操作を
行った。Example 5 In Example 1, PVA (UF-170M) was
The same operation was performed except that A (E-180) (manufactured by:'-NichihQ@, saponification degree 87 to 89 mol%) was used.
比較例5
実施例5において、撥水剤を塗布せずに100°Cで約
10分の熱処理を加えた以外は、同様の操作を行った。Comparative Example 5 The same operation as in Example 5 was performed except that a water repellent was not applied and heat treatment was applied at 100°C for about 10 minutes.
試験例
実施例1〜5で得られたフィルムの撥水剤処理を施した
面を内側にして、ヒートシールにて10cm角のバッグ
を作製した。同様に比較例1〜5のフィルムからも同様
のバッグを作成した。Test Example A 10 cm square bag was prepared by heat-sealing the films obtained in Examples 1 to 5 with the water-repellent treated side facing inside. Similarly, similar bags were created from the films of Comparative Examples 1 to 5.
各バッグに蒸留水30m1を加えて、どのように変化す
るかを観察した。結果を表−1に示す。30 ml of distilled water was added to each bag and the changes were observed. The results are shown in Table-1.
また、各フィルム10cm角を50m1の蒸留水に加え
、攪拌下に状況の変化を観察した。結果を表−2に示す
。Further, a 10 cm square of each film was added to 50 ml of distilled water, and changes in the situation were observed while stirring. The results are shown in Table-2.
表−1から明らかなように2本発明のバッグは。As is clear from Table 1, there are two bags of the present invention.
1時間以上の保水性を有しているので、携帯用採尿バッ
グ又はオスI・ミーバッグとして使用するに必要な保水
性を有しており、バッグに汚物を保持することができる
ことを示している。また1表−2から明らかように1本
発明のバッグは、水洗1〜イレにおいて7数十分後に水
に溶解ないしは分散し9通常の水洗トイI/に廃棄して
も3支障のない溶解性を有していることが分かる。Since it has a water retention property of 1 hour or more, it has the water retention property necessary for use as a portable urine collection bag or a male I/M bag, indicating that the bag can retain filth. In addition, as is clear from Table 1, the bag of the present invention dissolves or disperses in water after several tens of minutes from washing with water, and has a solubility that does not cause any problem even when disposed of in a normal flushing toy. It can be seen that it has
=18− 表−1容袋の保水状況 表−2各フィルムの溶解性 (発明の効果)=18- Table - Water retention status of 1-capacity bag Table-2 Solubility of each film (Effect of the invention)
Claims (2)
とポリビニルアルコールのゲル化促進剤とからなるフイ
ルムの片面に撥水剤がコーテイングされたフイルムから
なり,撥水剤がコーテイングされた面が内側となるよう
に成形された携帯用採尿バツグ。(1) A film made of polyvinyl alcohol with a degree of saponification of 70 to 98% and a polyvinyl alcohol gelling promoter, coated with a water repellent on one side, with the surface coated with the water repellent on the inside. A portable urine collection bag shaped like this.
とポリビニルアルコールのゲル化促進剤とからなるフイ
ルムの片面に撥水剤がコーテイングされたフイルムから
なり,撥水剤がコーテイングされた面が内側となるよう
に成形されたオストミーバツグ。(2) A film made of polyvinyl alcohol with a degree of saponification of 70 to 98% and a polyvinyl alcohol gelling promoter, coated with a water repellent on one side, with the surface coated with the water repellent on the inside. An ostomy bag shaped to
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2340565A JP3004351B2 (en) | 1990-11-30 | 1990-11-30 | Portable urine collection bag and ostomy bag |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2340565A JP3004351B2 (en) | 1990-11-30 | 1990-11-30 | Portable urine collection bag and ostomy bag |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04208162A true JPH04208162A (en) | 1992-07-29 |
JP3004351B2 JP3004351B2 (en) | 2000-01-31 |
Family
ID=18338211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2340565A Expired - Fee Related JP3004351B2 (en) | 1990-11-30 | 1990-11-30 | Portable urine collection bag and ostomy bag |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3004351B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2284820A (en) * | 1993-12-16 | 1995-06-21 | Kimberly Clark Co | Flushable compositions |
JPH1119108A (en) * | 1997-06-27 | 1999-01-26 | Alcare Co Ltd | Pouch for stoma outfit |
JPH11138700A (en) * | 1997-11-07 | 1999-05-25 | Nippon Synthetic Chem Ind Co Ltd:The | Water-soluble nonwoven fabric or woven fabric molded material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101749049B1 (en) * | 2015-05-13 | 2017-06-20 | 박갑환 | Excretion Cleaner |
-
1990
- 1990-11-30 JP JP2340565A patent/JP3004351B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2284820A (en) * | 1993-12-16 | 1995-06-21 | Kimberly Clark Co | Flushable compositions |
GB2284820B (en) * | 1993-12-16 | 1998-04-15 | Kimberly Clark Co | Flushable compositions |
JPH1119108A (en) * | 1997-06-27 | 1999-01-26 | Alcare Co Ltd | Pouch for stoma outfit |
JPH11138700A (en) * | 1997-11-07 | 1999-05-25 | Nippon Synthetic Chem Ind Co Ltd:The | Water-soluble nonwoven fabric or woven fabric molded material |
Also Published As
Publication number | Publication date |
---|---|
JP3004351B2 (en) | 2000-01-31 |
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