JPH0274694A - Paper having wet paper tenacity and water dispersibility and production thereof - Google Patents
Paper having wet paper tenacity and water dispersibility and production thereofInfo
- Publication number
- JPH0274694A JPH0274694A JP63224099A JP22409988A JPH0274694A JP H0274694 A JPH0274694 A JP H0274694A JP 63224099 A JP63224099 A JP 63224099A JP 22409988 A JP22409988 A JP 22409988A JP H0274694 A JPH0274694 A JP H0274694A
- Authority
- JP
- Japan
- Prior art keywords
- paper
- water
- wet
- binder
- wet paper
- 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 56
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 239000011230 binding agent Substances 0.000 claims abstract description 48
- 239000000835 fiber Substances 0.000 claims abstract description 31
- 150000001875 compounds Chemical class 0.000 claims abstract description 30
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 26
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 16
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000007127 saponification reaction Methods 0.000 claims abstract description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 38
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 38
- 238000002844 melting Methods 0.000 claims description 18
- 230000008018 melting Effects 0.000 claims description 17
- -1 alcohol compound Chemical class 0.000 claims description 8
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- 229920001451 polypropylene glycol Polymers 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 7
- 238000004090 dissolution Methods 0.000 abstract description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 150000001298 alcohols Chemical class 0.000 description 10
- 238000001035 drying Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 229940079593 drug Drugs 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 230000001476 alcoholic effect Effects 0.000 description 3
- 239000000730 antalgic agent Substances 0.000 description 3
- 239000003908 antipruritic agent Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 2
- ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 230000000202 analgesic effect Effects 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000013054 paper strength agent Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000004886 process control Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 2
- 229940034107 sulfazine Drugs 0.000 description 2
- 229940042585 tocopherol acetate Drugs 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- JCIIKRHCWVHVFF-UHFFFAOYSA-N 1,2,4-thiadiazol-5-amine;hydrochloride Chemical compound Cl.NC1=NC=NS1 JCIIKRHCWVHVFF-UHFFFAOYSA-N 0.000 description 1
- XWTUFPFWNHRJNF-UHFFFAOYSA-N 1,2-dimethylthianthrene Chemical compound C1=CC=C2SC3=C(C)C(C)=CC=C3SC2=C1 XWTUFPFWNHRJNF-UHFFFAOYSA-N 0.000 description 1
- WEEMDRWIKYCTQM-UHFFFAOYSA-N 2,6-dimethoxybenzenecarbothioamide Chemical compound COC1=CC=CC(OC)=C1C(N)=S WEEMDRWIKYCTQM-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- XPFCZYUVICHKDS-UHFFFAOYSA-N 3-methylbutane-1,3-diol Chemical compound CC(C)(O)CCO XPFCZYUVICHKDS-UHFFFAOYSA-N 0.000 description 1
- OFNXOACBUMGOPC-HZYVHMACSA-N 5'-hydroxystreptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](CO)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O OFNXOACBUMGOPC-HZYVHMACSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- IYLLULUTZPKQBW-UHFFFAOYSA-N Acrinol Chemical compound CC(O)C(O)=O.C1=C(N)C=CC2=C(N)C3=CC(OCC)=CC=C3N=C21 IYLLULUTZPKQBW-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- 241000276457 Gadidae Species 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000003332 Ilex aquifolium Nutrition 0.000 description 1
- 235000002296 Ilex sandwicensis Nutrition 0.000 description 1
- 235000002294 Ilex volkensiana Nutrition 0.000 description 1
- 239000008896 Opium Substances 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001139 anti-pruritic effect Effects 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- 229960001950 benzethonium chloride Drugs 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
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- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- VDQQXEISLMTGAB-UHFFFAOYSA-N chloramine T Chemical compound [Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 VDQQXEISLMTGAB-UHFFFAOYSA-N 0.000 description 1
- YZIYKJHYYHPJIB-UUPCJSQJSA-N chlorhexidine gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O.C1=CC(Cl)=CC=C1NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC1=CC=C(Cl)C=C1 YZIYKJHYYHPJIB-UUPCJSQJSA-N 0.000 description 1
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- 239000002537 cosmetic Substances 0.000 description 1
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- DNTGGZPQPQTDQF-XBXARRHUSA-N crotamiton Chemical compound C/C=C/C(=O)N(CC)C1=CC=CC=C1C DNTGGZPQPQTDQF-XBXARRHUSA-N 0.000 description 1
- 229960003338 crotamiton Drugs 0.000 description 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 1
- PHMMATAWQLJFIQ-UHFFFAOYSA-N cyanomercury(1+);oxygen(2-) Chemical compound [O-2].[Hg+]C#N.[Hg+]C#N PHMMATAWQLJFIQ-UHFFFAOYSA-N 0.000 description 1
- ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
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- RUQATQQNXCPTLL-PQMJGINDSA-N desoxymycin Chemical compound O1[C@@H](CO)[C@H](O)[C@@H](O)[C@H](NC)[C@@H]1O[C@@H]1[C@@H](CO)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O RUQATQQNXCPTLL-PQMJGINDSA-N 0.000 description 1
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical compound Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 229960003276 erythromycin Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
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- ACGUYXCXAPNIKK-UHFFFAOYSA-N hexachlorophene Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1CC1=C(O)C(Cl)=CC(Cl)=C1Cl ACGUYXCXAPNIKK-UHFFFAOYSA-N 0.000 description 1
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- 239000001257 hydrogen Substances 0.000 description 1
- OFNXOACBUMGOPC-UHFFFAOYSA-N hydroxystreptomycin Natural products CNC1C(O)C(O)C(CO)OC1OC1C(C=O)(O)C(CO)OC1OC1C(N=C(N)N)C(O)C(N=C(N)N)C(O)C1O OFNXOACBUMGOPC-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002497 iodine compounds Chemical class 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 229930027917 kanamycin Natural products 0.000 description 1
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- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 description 1
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- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229940096826 phenylmercuric acetate Drugs 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical class C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
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- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
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- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- 229960001544 sulfathiazole Drugs 0.000 description 1
- JNMRHUJNCSQMMB-UHFFFAOYSA-N sulfathiazole Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CS1 JNMRHUJNCSQMMB-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- LFAXYIHYMGEIHW-UHFFFAOYSA-N xyloylsulfamine Chemical compound C1=C(C)C(C)=CC=C1C(=O)NS(=O)(=O)C1=CC=C(N)C=C1 LFAXYIHYMGEIHW-UHFFFAOYSA-N 0.000 description 1
- 229950007039 xyloylsulfamine Drugs 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、容易に水に分散する紙であってかつ湿潤した
紙及びその製造方法に関する。更に詳しくは、ベビーワ
イパー クエットティッシュ、排便用ウェットティッシ
ュ等の湿潤状態で用いる各種ワイパー、生理用品、或い
は医療用手袋等の使い捨て製品として用いられ、水洗便
所等に廃棄され虎際に容易に水に分散して下水管内に閉
塞を生じない紙及びその製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a paper that is easily dispersible in water and is wet, and a method for producing the same. More specifically, it is used as a disposable product such as various wipers used in wet conditions such as baby wipes, wet wipes for defecation, sanitary products, or medical gloves, and is disposed of in flush toilets etc. and easily immersed in water. The present invention relates to paper that is dispersed and does not cause blockages in sewer pipes, and a method for producing the same.
〈従来技術〉
現在水で濡れた状態で使り紙及び不織布には湿濁時の紙
力を保持するために耐水性を向上させる工夫がなされて
いる。例えば紙などの場合には耐水性のあるエマルジョ
ンバインダーを用いたシ、湿潤紙力増強剤やエマルジョ
ン加工を施している。<Prior Art> Currently, paper and nonwoven fabrics used when wet with water have been devised to improve their water resistance in order to maintain paper strength when wet and muddy. For example, in the case of paper, a water-resistant emulsion binder is used, a wet paper strength agent is applied, and an emulsion process is applied.
また不織布の場合には水中絡合法、ニードルパンチ法、
更に熱溶融バインダー繊at用いたり、耐水性エマルジ
ョンバインダーを用いたシした化合*i不織布から出来
ている。これらは、当然耐水性を有するため水中分散性
は得られず水洗トイレへ流すことはできないものである
。例えば特開昭62−184193号公報に述べられて
いるが、水分散性はブロック状分散であシネ充分なもの
である。In addition, in the case of non-woven fabrics, underwater entanglement method, needle punch method,
Furthermore, it is made of a compound*i nonwoven fabric using heat-melting binder fibers or a water-resistant emulsion binder. Since these are naturally water resistant, they cannot be dispersible in water and cannot be flushed into a flush toilet. For example, as described in JP-A-62-184193, the water dispersibility is block-like dispersion, which is sufficient for cine.
t7’l−%開閉54−to4963 号公報には、P
vA含浸シートに硼酸等のゲル化剤を含有し九湿潤シー
トとし水中に流して処分する方法を提供している。t7'l-% open/close 54-to4963 publication includes P
A method is provided in which a vA-impregnated sheet contains a gelling agent such as boric acid to form a wet sheet and is disposed of by pouring it into water.
これとても毒性の強い硼酸を用いることから皮膚清浄材
としては好ましくない。This is not preferred as a skin cleansing material because it uses boric acid, which is highly toxic.
一方、水分散性の紙を得る方法としては、例えば特開昭
59−144426号公報の実施例に開示されているよ
うに、熱水可溶性のポリビニルアルコールを他の紙料と
共に混合し、湿式抄紙する方法がある。この方法によっ
て得られた紙は、混合したポリビニルアルコールが抄紙
後の乾燥工程において溶解し、他の紙料を接着固定して
バインダー効果を発揮しているが、水中に廃棄されると
ポリビニルアルコールが溶解し、紙が分散することとな
る。しかし用いるポリビニルアルコールが熱水には溶解
するが、冷水には溶解し難いものである場合、当然紙の
水分散性が悪くなシ、水洗便所の下水管を閉塞させるこ
ととなる。水分散性を向上さ斗るべく、冷水に溶解する
ポリビニルアルコールを用いた場合、ポリビニルアルコ
ールの抄紙時の溶解ロスが大きくなシ、抄紙時の排水処
理及び原材料費用等の経済的な損失が大きく、実用上不
可能である。On the other hand, as a method for obtaining water-dispersible paper, for example, as disclosed in the examples of JP-A No. 59-144426, hot water-soluble polyvinyl alcohol is mixed with other paper materials, and wet paper making is carried out. There is a way to do it. In the paper obtained by this method, the mixed polyvinyl alcohol dissolves in the drying process after papermaking and acts as a binder by adhering and fixing other paper materials, but when disposed of in water, the polyvinyl alcohol dissolves. It will dissolve and the paper will become dispersed. However, if the polyvinyl alcohol used is soluble in hot water but difficult to dissolve in cold water, the water dispersibility of the paper will naturally be poor and the sewage pipes in flush toilets will be clogged. When using polyvinyl alcohol that dissolves in cold water to improve water dispersibility, there is a large dissolution loss of polyvinyl alcohol during paper making, and economic losses such as wastewater treatment and raw material costs during paper making are large. , which is practically impossible.
tた特公昭55−38759号公報に示されているよう
に、熱水可解性のポリビニルアルコールバインダーを用
いる場合、その混合量を0.3〜1.5%と低下させて
紙の水分散性を確保する方法が考えられるが、この場合
、バインダー効果が充分発揮されないため、得られる紙
の紙力が低下すると共に、使用時紙粉の発生が著しく、
使用に耐えないという欠点がある。さらに、これら従来
の紙を湿潤紙とするべく水に湿潤させると、紙力が一層
低下することとなる。As shown in Japanese Patent Publication No. 55-38759, when a hydrothermally dissolvable polyvinyl alcohol binder is used, the mixing amount is reduced to 0.3 to 1.5% to improve water dispersion of paper. However, in this case, the binder effect is not sufficiently exerted, so the paper strength of the resulting paper decreases, and the generation of paper dust during use is significant.
The drawback is that it cannot withstand use. Furthermore, when these conventional papers are wetted with water to become wet paper, the strength of the paper is further reduced.
〈発明が解決しよりとする課題〉
本発明は、かかる従来技術の欠点を解消するものであっ
て、湿潤液としてアルコール系化合物で代表される湿潤
紙力保持剤含有液を用いた場合に湿潤紙力があり、かつ
水中分散性を有する紙であって、乾燥状態においても、
優れ走水分散性を有すると共に、使用に耐え得る充分な
紙力と柔軟でソフトな感触を有する水分散紙および経済
性、工程管理上優れた水分散紙の製造法を提供するもの
である。<Problems to be Solved by the Invention> The present invention solves the drawbacks of the prior art. A paper that is strong and dispersible in water, even in a dry state.
The present invention provides a water-dispersible paper that has excellent water running dispersibility, sufficient paper strength to withstand use, and a flexible and soft feel, and a method for producing the water-dispersible paper that is excellent in terms of economy and process control.
〈課題を解決するための手段〉
本発明は、ケン化度が90〜97.5モル−〇ポリビニ
ルアルコール系バインダー効果、 0〜20重量%、化
合繊維を10重量%以上含有し、且つ該ポリビニルアル
コール系バインダーが繊維状で存在して該化合繊維を結
合している紙、およびこの紙に含浸されている湿潤紙力
保持剤からなることを特徴とする湿潤紙力があシ、かつ
水中分散性を有する紙であ夛、更゛には、化合繊維を1
0重量−以上、溶解温度が50〜90℃で且つ潜在的溶
解温度が10〜40℃であるポリビニルアルコール(以
下PVAと略す)系轍維状バインダーを1.0〜20I
!量チ含有する紙料を湿式抄造した後、得られた紙に湿
潤紙力保持剤含有液を含浸することを特徴とする湿潤紙
力があ夛、かつ水中分散性を有する紙の製造方法である
。<Means for Solving the Problems> The present invention has a degree of saponification of 90 to 97.5 mol - polyvinyl alcohol binder effect of 0 to 20% by weight, contains compound fibers of 10% by weight or more, and A paper with low wet paper strength and water dispersion, characterized by comprising a paper in which an alcoholic binder exists in the form of fibers to bind the compound fibers, and a wet paper strength retaining agent impregnated in this paper. It is made of paper that has properties, and one layer of compound fiber is added
0 weight or more, a polyvinyl alcohol (hereinafter abbreviated as PVA)-based fibrous binder having a melting temperature of 50 to 90°C and a potential melting temperature of 10 to 40°C.
! A method for producing paper with high wet paper strength and dispersibility in water, which comprises wet-forming a paper stock containing a certain amount of water, and then impregnating the obtained paper with a liquid containing a wet paper strength retaining agent. be.
湿潤紙力保持剤とは、それを含む液を前記紙に含浸する
ことによシ、含浸され九湿潤紙の紙力が大きく低下する
ことを防ぐことができる化合物を意味しておシ、次に示
すアルコール系化合物で代表される。すなわちアルコー
ル系化合物とは、1価、、2価、3価あるいはそれ以上
の多価アルコールならびに、ポリエチレングリコールや
ポリプロピレングリコールで代表されるポリオキシアル
キレングリコールであシ、水溶性である化合物が好まし
い。Wet paper strength retaining agent means a compound that can prevent the paper strength of wet paper from being significantly reduced by impregnating the paper with a liquid containing it. It is represented by the alcohol-based compounds shown below. That is, the alcoholic compound is preferably a water-soluble compound such as monovalent, divalent, trivalent or higher polyhydric alcohol, and polyoxyalkylene glycol represented by polyethylene glycol or polypropylene glycol.
これら湿潤紙力保持剤を含有した、水中分散性がちり、
使用に耐える紙力と柔軟でかつンフトな感触を有する水
分散紙及びその製造方法について説明する。Water-dispersible dust containing these wet paper strength retention agents,
A water-dispersed paper that has paper strength that can withstand use, is flexible, and has a soft feel, and a method for manufacturing the same will be described.
ここで、PVA系H1維状バインダーの潜在的溶解温度
とは、該PVA系繊維状バインダーを製造−する際乾燥
のみ行ない、熱処理を施さない状態に於ける該バインダ
ーの溶解温度であり、後述の如く該バインダーを用いて
得られた水中分散紙に於けるPVA系バインダーの溶解
温度と一致する。Here, the potential melting temperature of the PVA-based H1 fibrous binder is the melting temperature of the PVA-based fibrous binder in a state in which only drying is performed and no heat treatment is performed when manufacturing the PVA-based fibrous binder. This corresponds to the melting temperature of the PVA binder in the water-dispersed paper obtained using the binder.
本発明に用いられるPVA系繊維状バインダーは、ケン
化度90〜97.5モルチのPVAの水溶芒
夜を・硝等の塩類浴を凝固浴として常法により湿式紡糸
シ、念後通常105〜140℃で乾燥し、更に溶解温度
が前述の50〜90℃になる如く通常160〜250℃
で熱処理した後適当な繊維長に切断して得られるが、紡
糸后の乾燥のみでは繊維状を保持しているもののその溶
解温度は10〜40℃であシ極めて水溶解性に富むもの
である。紙の抄造工程では、前述の熱処理後のPVA系
繊維状バインダーは一旦湿式抄造され、通常110〜3
.30℃で加熱乾燥される。この乾燥工程で抄造時に保
持した水分と乾燥時の加熱によシ該バインダーは溶解し
、バインダー効果を発揮するが、溶解後は、前記紡糸后
の乾燥と同穆度の温度で乾燥される九め、上記紡糸后の
乾燥後の溶解温度に対応する低い溶解温度(すなわち潜
在的溶解温度)を示す(て至る。これは紡糸乾燥後の熱
処理によって一時的に与えられる該PVA系繊維状バイ
ンダーの耐水性が消滅することによる。以上述べた如く
、本来極めて水溶性に富んだケン化度90〜97.5モ
ルチのPVAを用い、繊維形成後の熱処理によって一時
的に耐水性を与えて湿式抄造の際の溶解ロスを抑制して
経済的に優れ且つ、工程管理を容易ならしめるPVA系
繊維状バインダーを用い、抄造后の乾燥工程で再び水溶
性に富んだPVA系バインダーとして紙中に存在せしめ
るという巧妙な技術が本発明の根幹であシ、従って、本
発明の水中分散紙及びその製造方法は従来の技術には見
られない全く新規な技術である。The PVA-based fibrous binder used in the present invention is wet-spun by a conventional method using a water-soluble PVA solution having a saponification degree of 90 to 97.5 molt and a salt bath such as sulfur as a coagulation bath. Dry at 140°C, and then dry at usually 160°C to 250°C so that the melting temperature is 50°C to 90°C.
It is obtained by heat-treating it with water and then cutting it into appropriate fiber lengths. Although it retains its fibrous form only by drying after spinning, its melting temperature is 10 to 40°C and it is highly water-soluble. In the papermaking process, the PVA-based fibrous binder after the above-mentioned heat treatment is once wet-processed and usually has a
.. It is heated and dried at 30°C. In this drying process, the binder is dissolved by the moisture retained during papermaking and the heating during drying, and exhibits a binder effect. Therefore, the PVA-based fibrous binder exhibits a low melting temperature (i.e., potential melting temperature) corresponding to the melting temperature after drying after spinning. This is due to loss of water resistance.As mentioned above, wet papermaking is performed by using PVA with a saponification degree of 90 to 97.5 moles, which is originally extremely water-soluble, and temporarily imparting water resistance through heat treatment after fiber formation. We use a PVA-based fibrous binder that suppresses dissolution loss during papermaking, is economically superior, and facilitates process control, and is re-presented in the paper as a highly water-soluble PVA-based binder during the drying process after papermaking. This ingenious technique is the basis of the present invention, and therefore, the underwater dispersion paper of the present invention and its manufacturing method are completely new techniques not seen in the prior art.
本発明の第2の特長は、湿潤紙力保持剤を好ましくは1
0%以上(重量に基づく値であって、以下慢は重量慢で
ある)含む溶液に前述の水溶解性紙を浸漬して濡れた状
態で使える紙でかつ水洗トイレに流すことができる水分
散性紙としたことである。湿潤紙力保持剤としては、P
vAの溶剤又は可塑剤として水に次ぐ良溶剤である三価
アルコール、たとえばグリセリン、ペトリオール%t−
+二価アルコールのブタンジオールなどの水溶液、又は
ポリオキシアルキレングリコールであるボリエfレンク
リコール’?ホリ7’ロビレングリコールの溶液、また
はこれに水を加えた混合溶液が好適な代表例として用い
られ、これに前述の水中分散紙を含浸しても、驚くべき
ことに、湿潤紙力保持液中では使用に耐え得る充分な紙
力を有していることを見出した。これら湿潤紙力保持剤
がPVAの水溶性を阻害する理由は不明であるが、不思
議なことに大量の水が存在する場合には水に容易に溶解
する性質を有する。すなわち本発明は、前述したような
新規なPVAバインダーと、PVAの溶剤となシ得るア
ルコール系化合物等の混合水溶液の利用の二つの相乗効
果を見出して初めて得られたものである。A second feature of the present invention is that the wet paper strength agent is preferably
Water-dispersed paper that can be used in a wet state by immersing the water-soluble paper mentioned above in a solution containing 0% or more (values based on weight, hereinafter referred to as weight-based) and that can be flushed into a flush toilet. This is because it was made into a sex paper. As a wet paper strength retaining agent, P
Trihydric alcohols, which are second only to water as solvents or plasticizers for vA, such as glycerin, petriol% t-
+Aqueous solutions of dihydric alcohols such as butanediol, or polyoxyalkylene glycols'? A solution of holly 7' robylene glycol or a mixed solution thereof with water is used as a suitable representative example, and even if the above-mentioned water-dispersed paper is impregnated with this solution, surprisingly, the wet paper strength retaining solution It was found that the paper had sufficient strength to withstand use. The reason why these wet paper strength retaining agents inhibit the water solubility of PVA is unknown, but strangely, they have the property of easily dissolving in water when a large amount of water is present. That is, the present invention was first achieved by discovering the synergistic effect of the above-mentioned novel PVA binder and the use of a mixed aqueous solution of an alcoholic compound or the like that can act as a solvent for PVA.
本発明のPVA系繊維状バインダーのケン化度は90〜
97.5モルチであり、90モル多未満では水溶性は優
れているものの前述の紡糸后の乾燥工程で繊維が膠着し
製造不能であり、オた97.5モルチを越えると紡糸乾
燥のみで耐水性が附与され抄造乾燥后も充分な水溶性が
得られず、従って得られた紙の水中分散性が悪くなる。The degree of saponification of the PVA-based fibrous binder of the present invention is from 90 to
If it is less than 90 moles, the water solubility is excellent, but the fibers will stick together in the drying process after spinning as described above, making it impossible to manufacture. Even after papermaking and drying, sufficient water solubility cannot be obtained, and the resulting paper has poor dispersibility in water.
ま九本発明の水中分散紙中に含有されるPVA系バイン
ダーは1〜20重量%である。1重量%(以下特に記さ
ない限夛チは重量%である)未満では充分な紙力が得ら
れないばかシでなく、他の紙料を充分結合接着出来ない
ため、使用時に紙粉が多発する。また2 0 Xi%を
越える場合には水中分散性が悪くなると共に得られる紙
が疎開になシ、触感が損われる。好ましくは3〜7%で
ある。(9) The PVA binder contained in the water-dispersed paper of the present invention is 1 to 20% by weight. If it is less than 1% by weight (unless otherwise specified, all percentages are by weight), sufficient paper strength cannot be obtained, and other paper materials cannot be bonded together sufficiently, resulting in a large amount of paper dust during use. do. If it exceeds 20 Xi%, the dispersibility in water will be poor and the paper obtained will not be loose and the texture will be impaired. Preferably it is 3 to 7%.
般に紙中のPVA系バインダーの含有量を増加させると
、紙力の向上と共に疎開感が増して来る九めPVA粉末
で混抄したシ、又紙にPVA系等の樹脂を塗布する従来
の方法では紙力を犠牲にして柔軟性を保持しなければな
らなかったが、本発明の如(PVA系繊維状バインダー
を用い紙中のバインダーを繊維状で点在させるとバイン
ダーが他の紙料全面を被覆しないため、バインダー量が
増加しても疎開感が現れ難く柔軟でソフトな感触の紙が
得られる。In general, when the content of PVA binder in paper is increased, the paper strength improves and the feeling of looseness increases. However, when using the present invention (using a PVA-based fibrous binder and interspersing the binder in the paper in the form of fibers), the binder spreads over the entire surface of other paper materials. Since the binder is not coated, even if the amount of binder is increased, the feeling of looseness is less likely to appear, and a paper with a flexible and soft feel can be obtained.
淘本発明のPVA系繊維状バインダーの繊度、繊維長は
特に限定されるものではないが、好ましくはそれぞれ1
.0〜2.0デニール、2〜10鱈である。The fineness and fiber length of the PVA-based fibrous binder of the present invention are not particularly limited, but each is preferably 1
.. 0 to 2.0 denier, 2 to 10 cod.
本発明の水中分散紙を構成する化合繊維は特に限定され
ず、PVA系、ポリエステル系、セルローズ系、ポリオ
レフィン系、ポリアミド系、アクリル糸環各種の化合繊
維を用いることが出来る。The compound fibers constituting the underwater dispersion paper of the present invention are not particularly limited, and various types of compound fibers such as PVA-based, polyester-based, cellulose-based, polyolefin-based, polyamide-based, and acrylic thread rings can be used.
またその繊度及び繊維長も特に限定されるものでなく、
用途に応じて適宜使い分ければよいが、得られる水中分
散紙の触感の点で好ましくは0.2〜3デニール、2〜
1O1alである。Also, the fineness and fiber length are not particularly limited,
It may be used as appropriate depending on the purpose, but from the viewpoint of the feel of the obtained underwater dispersion paper, preferably 0.2 to 3 deniers and 2 to 3 deniers.
1O1al.
化合繊維の含有量も又触感を左右し、柔軟で)7トな触
感を得る念めには少くとも10%以上の化合4Rmを含
有する必要がある。化合42m以外に用いられる紙料と
しては経済性、抄造性の点で主として各種天然パルプが
好ましいが、他の紙料全混合する場合も含めて化合PJ
、維10%未満では紙の柔軟さが損われ、所謂ペーパー
ライクで疎開な感触を与える。The content of compound fibers also affects the feel, and in order to obtain a soft and soft feel, it is necessary to contain at least 10% of the compound 4Rm. Various natural pulps are mainly preferred as the paper stock to be used other than Compound 42m from the viewpoint of economy and paper-making properties, but Compound PJ
If the fiber content is less than 10%, the flexibility of the paper will be impaired, giving it a so-called paper-like and loose feel.
湿潤紙力保持剤としてのアルコール系化合物としては、
まず1価のアルコール、具体的には、メタノール、エタ
ノール、グロバノール、ブタノール、プロピルアルコー
ル、インフロビルアルコール等の水溶性を示す直鎖状ま
之は分岐状アルコール類、また2価のアルコール、具体
的には、エチレングリコール、フロパンジオール、3−
メチルブタン−1,3−ジオール、ヘキシレングリコー
ル、プロピレングリコール、1.3−ブタンジオール等
の水溶性を示すアルコール類、そして3価のアルコール
、具体的には、グリセリン、ペトリオール(すなわち3
−メチルペンタン−1,3,5−)ジオール)等の水溶
性を示すアルコール類、そしてジエチレングリコール、
ポリエチレングリコール、ポリプロピレングリコール等
の水溶性ポリオキシアルキレングリコールが挙げられる
。Alcohol-based compounds as wet paper strength retention agents include:
First, monohydric alcohols, specifically water-soluble linear or branched alcohols such as methanol, ethanol, globanol, butanol, propyl alcohol, and inflobil alcohol, and dihydric alcohols, specifically Specifically, ethylene glycol, furopanediol, 3-
Water-soluble alcohols such as methylbutane-1,3-diol, hexylene glycol, propylene glycol, and 1,3-butanediol, and trihydric alcohols, specifically glycerin, petriol (i.e.,
-methylpentane-1,3,5-) diol), and diethylene glycol;
Examples include water-soluble polyoxyalkylene glycols such as polyethylene glycol and polypropylene glycol.
これら湿潤紙力保持剤の水への混入割合は多い方が紙力
保持効果は高いが、混入なしの場合水となり、紙は水分
散してしまう。その念め櫨々混合率を検討した結果、湿
潤紙力保持剤は液中に少くとも10%混合されているこ
とが望ましく、10チ未満では水の影響が大きく湿潤紙
力保持の点から好ましくない。よシ好ましくは40%以
上混合されている場合である。The greater the proportion of these wet paper strength retaining agents mixed in with water, the higher the paper strength retaining effect, but if they are not mixed in, water will form and the paper will be dispersed in water. As a result of careful consideration of the mixing ratio, we found that it is desirable that the wet paper strength retention agent be mixed in the liquid at least 10%; less than 10% is preferable from the viewpoint of wet paper strength retention because the influence of water is large. do not have. More preferably, it is a case where the content is 40% or more.
本発明の湿潤紙を人体清浄に用いるためには。In order to use the wet paper of the present invention for human body cleaning.
使用する部位によっても異るが、化粧品原料基準、又は
日本薬局方規格に適合する安全上問題のない湿潤紙力保
持剤、具体的にはグリセリン、3−メチルブタン−1,
3−ジオール、プロピレングリコール、1.3−ブタン
ジオール、ポリエチレングリコール等が用いられる。そ
の他スクヮランやゲラニオールなども湿潤紙力保持剤と
して、あるいはその他の添加剤として用いることができ
る。Although it varies depending on the part used, wet paper strength retention agents that meet the cosmetic raw material standards or the Japanese Pharmacopoeia standards and have no safety problems, specifically glycerin, 3-methylbutane-1,
3-diol, propylene glycol, 1,3-butanediol, polyethylene glycol, etc. are used. In addition, squalane, geraniol, and the like can also be used as wet paper strength retaining agents or as other additives.
また医薬用剤を含浸することも可能で、たとえばクロタ
ミトン(クロトニル−N−エチル−〇−トルイジン)l
OOWllb ヒドロコルチゾン2.5■、酢酸トコフ
ェロール(ビタミンEアセテート)5岬をlf中に含む
、湿疹等の皮膚疾患に好適な市販系(商品名:オイラツ
クス)を水で溶かしたもの、グルコン酸クロルヘキシジ
ン液(20%)1チと軟膏基剤99チからなる皮フ疾患
・外傷治療剤に好適な市販薬(商品名:オロナインHv
k膏)を水で溶かしたものなどを用いることもできる。It is also possible to impregnate medicinal agents, for example, crotamiton (crotonyl-N-ethyl-〇-toluidine) l.
OOWllb A commercially available system suitable for skin diseases such as eczema (trade name: Euratus) containing 2.5 ■ hydrocortisone and 5 caps of tocopherol acetate (vitamin E acetate) dissolved in water, chlorhexidine gluconate solution ( A commercially available drug (product name: Oronine Hv
It is also possible to use a solution prepared by dissolving K. ointment) in water.
この他にも種々の外用薬が適用し得る。例えば殺菌薬、
鎮痛鎮痒薬、皮膚刺激薬等が用いられる。In addition to these, various external medicines can be applied. For example, bactericides,
Analgesics, antipruritics, skin irritants, etc. are used.
例えば殺菌薬としては具体的には、メタノール、エタノ
ール、インプロパツール等のアルコール類、硫酸オキシ
キノリン酸等のオキシキノリン誘導体、ホウ酸、ホウ酸
ナトリウム等のホウ酸ないしその誘導体、アクリノール
、過酸化水素水、オキシシアン化水銀等の過酸化水素な
いしその誘導体、フェノール、クレゾール、レゾルシン
等のフェノールないしその誘導体、安息香酸、安息香酸
ナトリウム、安息香酸ベンジル等の安息香酸ないしその
誘導体、塩化ベンザルコニウム、塩化ベンゼトニウム等
のカチオン性界面活性剤、塩化第一水銀、塩化第二水銀
、黄色酸化水銀、酢酸フェニル水銀、チメロサール等の
水銀含有有機化合物、その他硝酸銀、ヨウ素ないしヨウ
素化合物、チアントール(ジメチルチアントレンおよび
ジトルエンジスルフイド)塩化メチルロザニリン、クロ
ラミンT。For example, specific disinfectants include alcohols such as methanol, ethanol, and impropatol, oxyquinoline derivatives such as oxyquinolinic acid sulfate, boric acid and its derivatives such as boric acid, sodium borate, acrinol, and peroxide. Hydrogen water, hydrogen peroxide or its derivatives such as mercuric oxycyanide, phenol, phenol or its derivatives such as cresol, resorcinol, benzoic acid or its derivatives such as benzoic acid, sodium benzoate, benzyl benzoate, benzalkonium chloride , cationic surfactants such as benzethonium chloride, mercury-containing organic compounds such as mercurous chloride, mercuric chloride, yellow mercury oxide, phenylmercuric acetate, thimerosal, other silver nitrate, iodine or iodine compounds, thianthole (dimethylthianthrene) and ditoluene disulfide) methylrosaniline chloride, chloramine T.
ヘキサクロロフェン、ニトロフラゾンなどの種々のもの
がある。ま念キシロイルスルファミン、スルファアジン
、スルファミン、スルファチアゾール、スルファアジン
、スルフィンキサゾール、スルフィンミジン、フタリル
スルファデアゾール等のサルファ剤、エリスロマイシン
、クロムフェニコール、カナマイシン、硫酸カナマイシ
ン、硫酸ストレプトマイシン、硫酸ジヒドロデオキシス
トレプトマイシン、硫酸ヒドロキシストレプトマイシン
等の抗生物質分散液等も使用可能である。There are various types such as hexachlorophene and nitrofurazone. Sulfa drugs such as xyloylsulfamine, sulfazine, sulfamine, sulfathiazole, sulfazine, sulfinxazole, sulfinmidine, phthalylsulfadeazole, erythromycin, chromphenicol, kanamycin, kanamycin sulfate, streptomycin sulfate, dihydrodeoxystreptomycin sulfate, Antibiotic dispersions such as hydroxystreptomycin sulfate can also be used.
これらの化合物のうち用途に応じて適宜の好ましい薬剤
を選択すれば良い。また鎮痛鎮痒剤および皮膚刺激系と
しても各種の薬剤が使用されるものであるが、例えば、
鎮痛鎮痒剤としては、チョウジ油、ベンジルアルコール
あるいはアヘンアルカロイド等が、また皮膚刺激系とし
ては、カンフル、サリチル酸およびサリチル酸エステル
、t−メント−huよo:、t−メントールエステル、
アンモニア、イソチオシアン酸エステル等がある。また
捕々の芳香剤を庭加することも可能である。Among these compounds, an appropriate and preferable drug may be selected depending on the intended use. Various drugs are also used as analgesic and antipruritic agents and skin stimulants, such as:
Examples of analgesic and antipruritic agents include clove oil, benzyl alcohol, and opium alkaloids; examples of skin irritation agents include camphor, salicylic acid and salicylic acid esters, t-menth-huyo:, t-menthol ester,
Examples include ammonia and isothiocyanate esters. It is also possible to add fresh fragrances.
以上列記した多くの化合物のうち、アルコール類に属す
る化合物は、湿潤紙力保持剤としての働きをも有する。Among the many compounds listed above, compounds belonging to alcohols also function as wet paper strength retaining agents.
またアルコール類以外の化合物であっても、それが湿潤
時の紙力の大幅な低下金時ぐことかできる化合物である
ならば、それも本発明で言う湿潤紙力保持剤に含まれる
。Further, even if the compound is other than alcohols, if it is a compound that can significantly reduce paper strength when wet, it is also included in the wet paper strength retaining agent as referred to in the present invention.
次に本発明を実施例によって更に具体的に説明する。Next, the present invention will be explained in more detail with reference to Examples.
淘、本発明は以下述べる実施例に限定されるものではな
い。However, the present invention is not limited to the embodiments described below.
実施例1
ケン化度96.0モルチ、平均重合度1700のPIA
粉末を16慢水溶液とし、これを孔径0.08芒
国、孔数6000の口金から40℃の飽和・硝浴中で
に紡糸し、得られ九糸条を90℃の飽和・硝浴中で2.
0倍のドラフトをかけ九後120℃で乾燥し更に180
℃で熱処理して単繊維繊度が1.0デニールの篠を得喪
。これをffi維長3■に切断し、PVA系繊維状バイ
ンダーを得九。Example 1 PIA with saponification degree of 96.0 molar and average polymerization degree of 1700
The powder was made into a 16% aqueous solution, which was spun in a saturated glass bath at 40°C from a spinneret with a pore size of 0.08 mm and 6000 holes, and the resulting nine threads were spun in a saturated glass bath at 90°C. 2.
Dry at 120℃ after 90 minutes with a 0x draft, and then dry at 180℃.
Shino with a single fiber fineness of 1.0 denier is obtained by heat treatment at ℃. This was cut into ffi fiber lengths of 3 to obtain a PVA-based fibrous binder.
同、得られたPVA系繊維状バインダーの溶解温1tは
60°Cであシ、ま念潜在的溶解温度、即ち上記紡糸、
乾燥后の溶解温度は15℃であつ之。The melting temperature 1t of the obtained PVA-based fibrous binder is 60°C.
The melting temperature after drying is 15°C.
この様にして得られ九PVA系繊維状バインダー3%、
繊度2.0デニール、繊維長5喝のポリエステルfRm
(クラレ社製EP203X5)479b及びカナダ標準
f水度710dの針葉樹パルプ(NBKP)50%を混
合して紙料とし、短網型ワイヤーを備えた湿式抄造材を
用いて常法によシ抄紙した後、110℃のヤンキー型ド
ライヤーで乾燥し、坪量30.5f/m”水中分散紙を
得九。Nine PVA-based fibrous binders obtained in this way, 3%;
Polyester fRm with a fineness of 2.0 denier and a fiber length of 5 mm.
(Kuraray EP203 After that, it was dried in a Yankee type dryer at 110°C to obtain a water-dispersed paper with a basis weight of 30.5 f/m.
次に湿潤紙力保持剤として重合度400のポリプロピレ
ングリコールを用い、水を加え、混合水溶液濃度を、1
0チ、20チ、40160%、100%とし、上記試作
した紙を浴比11000になるように20℃、24時間
浸漬した。浸漬后浴中から手で取)出し、水滴が落下し
なくなった時の紙の強力を測定し、湿潤時使用の可否の
判定をした。更にこの紙の水中分散性を判定する/とめ
に水100CCを入れた200CC容エレマイヤーフラ
スコに直径7鱈、長さ3Qmの円筒形の回転子を入れて
マグネチツクスタージー上に載せ、回転子が500RP
M±2ORPMになる様調整する。−辺7txの正方形
に裁断した水中分散性紙をエレマイヤーフラスコ中に投
入し1紙の原形をとどめ々く々る迄の時間を計測し、次
の如く表す。この結果を第1異に示す。Next, using polypropylene glycol with a degree of polymerization of 400 as a wet paper strength retaining agent, water was added to bring the concentration of the mixed aqueous solution to 1.
The sample paper was immersed at 20° C. for 24 hours at a bath ratio of 11,000. After soaking, the paper was removed from the bath by hand, and the strength of the paper was measured when water droplets stopped falling, and it was determined whether or not it could be used when wet. Furthermore, to determine the dispersibility of this paper in water, a cylindrical rotor with a diameter of 7 cods and a length of 3 Qm was placed in a 200 cc Ellemeyer flask containing 100 cc of water and placed on a magnetic stirrer. is 500RP
Adjust so that it becomes M±2ORPM. - A water-dispersible paper cut into a square with a side of 7 tx was put into an Elemeyer flask, and the time required to completely remove the original shape of one paper was measured and expressed as follows. This result is shown in the first difference.
◎ : 10秒以内
○ : 30秒以内
Δ : 1分以内
× : 1分以上
なお本発明で言う物性または物性の測定方法は次の通シ
である。◎: Within 10 seconds ○: Within 30 seconds Δ: Within 1 minute ×: 1 minute or more The physical properties or methods for measuring physical properties referred to in the present invention are as follows.
l)溶解ロス率
抄造に供したバインダーの混合比率(A)及び得られた
水中分散性紙の煮沸減量から求めたバインダー混合比率
(B)から次式によって求めた。l) Dissolution loss rate The dissolution loss rate was determined by the following formula from the blending ratio (A) of the binder used in papermaking and the binder blending ratio (B) determined from the boiling loss of the obtained water-dispersible paper.
八
2)PVA系R維状バインダーの溶解温度切断層の繊維
状バインダー2Fを5℃の水1007中に分散させ毎分
1℃で水温を上昇させ完全に愼維状物が・・・溶解した
ときの温度で表わす。82) Melting temperature of PVA-based R fibrous binder The fibrous binder 2F of the cutting layer was dispersed in water 1007 at 5°C, and the water temperature was raised at 1°C per minute until the fibrous material was completely dissolved. It is expressed as the temperature at that time.
3)紙裂断長
JIS P−8113に準じて判定し、タテ、ヨコの平
均値で示した。3) Paper tear length was determined according to JIS P-8113, and was expressed as an average value for length and width.
4)湿潤時の使用の可否の判定
湿潤処理するため水溶性シートを浸漬し、湿紙強力が弱
く手で取りあつか兄ないものをX印とし、取シ出し、紙
を折シたたんで手等を清拭した時毛羽の発生、紙の切れ
等の起らず強くふけるものを◎印とした。その中間で、
清拭時普通に取シ扱えるものを○印とした。4) Determining whether or not it can be used when wet Dip a water-soluble sheet into the wet sheet for wet treatment, mark the wet paper with a weak X mark if it is weak and cannot be handled by hand, take it out, and fold the paper. A mark of ◎ was given to those that were heavily indulging in without causing fuzz or paper cuts when wiping hands, etc. In the middle,
Items that can be handled normally during cleaning are marked with an ○.
比較例1
ケン化度98.5モルチ、平均重合度1700のPVA
粉末を用い、実施例1とまったく同じ方法で繊維状バイ
ンダーを得た。Comparative Example 1 PVA with saponification degree of 98.5 molt and average polymerization degree of 1700
A fibrous binder was obtained using the powder in exactly the same manner as in Example 1.
尚得られた繊維状バインダーの溶解温度は60℃であシ
、a在的溶解温度は45℃であった。該繊維状バインダ
ーを用い実施例1とまったく同じ方法により坪量31.
Ot/ m’の紙を得た。その後の処理、評価も実施例
1と同様に実施[7た。これを第1表に示した。The melting temperature of the obtained fibrous binder was 60°C, and the actual melting temperature was 45°C. The fibrous binder was used in exactly the same manner as in Example 1 to obtain a basis weight of 31.
A paper of Ot/m' was obtained. The subsequent treatments and evaluations were carried out in the same manner as in Example 1 [7]. This is shown in Table 1.
このように本発明の実施例1は湿潤強力もあシはぼ清拭
用として使用ができ、かつ水分散性のあるものである。As described above, Example 1 of the present invention can be used as a strong wet wiper for wiping and has water dispersibility.
それに対し、比較例1の場合は湿潤紙力は満足するが、
耐水性に優れているため水分散性は得られない。On the other hand, in the case of Comparative Example 1, the wet paper strength is satisfactory, but
Because it has excellent water resistance, water dispersibility is not obtained.
実施例2
実施例1で示したポリエステル繊維に代えて礒度1.5
デニール、繊維長5mのレーヨン繊′m(大和紡製レー
ヨン 3D1.5X5)を用い、実襖例】と同様にして
坪量31.2f/rn’の水中分散紙を得た。Example 2 In place of the polyester fiber shown in Example 1, the fragility was 1.5.
A water-dispersed paper with a basis weight of 31.2 f/rn' was obtained in the same manner as in Example] using rayon fibers (rayon 3D1.5X5 manufactured by Daiwabo Co., Ltd.) having a denier and a fiber length of 5 m.
また湿潤紙力保持剤として水とグリセリンの混合溶液と
し、グリセリン濃度を】0%、20%、40%、60%
、100%とし、他は実施例1とまったく同じ方法で処
理し、湿潤紙力及び水分散性を評価した。In addition, a mixed solution of water and glycerin is used as a wet paper strength retaining agent, and the glycerin concentration is 0%, 20%, 40%, and 60%.
, 100%, and otherwise treated in exactly the same manner as in Example 1, and wet paper strength and water dispersibility were evaluated.
その結果を第2表に示す。The results are shown in Table 2.
以下余白
第
表
上記結果よシ明らかなように、湿潤紙力保持剤(グリセ
リン)によ)湿潤時使用可能なシートが得られておシ、
なお水分散性があるものであり之。As is clear from the above results, it is possible to obtain a sheet that can be used when wet with the wet paper strength retaining agent (glycerin).
Note that it is water-dispersible.
Claims (1)
コール系バインダーを1.0〜20重量%、化合繊維を
10重量%以上含有し、且つ該ポリビニルアルコール系
バインダーが繊維状で存在して該化合繊維を結合してい
る紙、およびこの紙に含浸されている湿潤紙力保持剤か
らなることを特徴とする湿潤紙力があり、かつ水中分散
性を有する紙。 2、湿潤紙力保持剤がアルコール系化合物である請求項
1に記載の紙。 3、湿潤紙力保持剤が、エチレングリコール、プロピレ
ングリコール、ポリエチレングリコールおよびポリプロ
ピレングリコールからなる群から選ばれる少なくとも1
種の化合物である請求項1に記載の紙。 4、化合繊維を10重量%以上、溶解温度が50〜90
℃で且つ潜在的溶解温度が10〜40℃であるポリビニ
ルアルコール系繊維状バインダーを1.0〜20重量%
含有する紙料を湿式抄造した後、得られた紙に湿潤紙力
保持剤含有液を含浸することを特徴とする湿潤紙力があ
り、かつ水中分散性を有する紙の製造方法。 5、湿潤紙力保持剤がアルコール系化合物である請求項
4に記載の製造方法。 6、湿潤紙力保持剤が、エチレングリコール、プロピレ
ングリコール、ポリエチレングリコールおよびポリプロ
ピレングリコールからなる群から選ばれる少なくとも1
種の化合物である請求項4に記載の製造方法。[Scope of Claims] 1. Contains 1.0 to 20% by weight of a polyvinyl alcohol binder with a degree of saponification of 90 to 97.5 mol%, and 10% by weight or more of compound fibers, and the polyvinyl alcohol binder A paper having wet paper strength and dispersibility in water, characterized by comprising paper existing in the form of fibers and binding the compound fibers, and a wet paper strength retaining agent impregnated into the paper. 2. The paper according to claim 1, wherein the wet paper strength retaining agent is an alcohol compound. 3. The wet paper strength retaining agent is at least one selected from the group consisting of ethylene glycol, propylene glycol, polyethylene glycol, and polypropylene glycol.
The paper according to claim 1, which is a compound of seeds. 4. Compound fiber at 10% by weight or more, melting temperature 50-90
1.0 to 20% by weight of a polyvinyl alcohol-based fibrous binder having a potential melting temperature of 10 to 40°C.
1. A method for producing paper having wet paper strength and dispersibility in water, which comprises wet paper forming a paper stock containing the same, and then impregnating the obtained paper with a liquid containing a wet paper strength retaining agent. 5. The manufacturing method according to claim 4, wherein the wet paper strength retaining agent is an alcohol compound. 6. The wet paper strength retaining agent is at least one selected from the group consisting of ethylene glycol, propylene glycol, polyethylene glycol, and polypropylene glycol.
The manufacturing method according to claim 4, which is a seed compound.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63224099A JP2604436B2 (en) | 1988-09-06 | 1988-09-06 | Paper having wet paper strength and dispersibility in water and method for producing the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63224099A JP2604436B2 (en) | 1988-09-06 | 1988-09-06 | Paper having wet paper strength and dispersibility in water and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0274694A true JPH0274694A (en) | 1990-03-14 |
JP2604436B2 JP2604436B2 (en) | 1997-04-30 |
Family
ID=16808530
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63224099A Expired - Lifetime JP2604436B2 (en) | 1988-09-06 | 1988-09-06 | Paper having wet paper strength and dispersibility in water and method for producing the same |
Country Status (1)
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JP (1) | JP2604436B2 (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5558873A (en) * | 1994-06-21 | 1996-09-24 | Kimberly-Clark Corporation | Soft tissue containing glycerin and quaternary ammonium compounds |
US5601871A (en) * | 1995-02-06 | 1997-02-11 | Krzysik; Duane G. | Soft treated uncreped throughdried tissue |
WO1997013920A1 (en) * | 1995-10-13 | 1997-04-17 | Uni-Charm Corporation | Biodegradable and hydrolyzable sheet |
US5650218A (en) * | 1995-02-06 | 1997-07-22 | Kimberly-Clark Corporation | Soft treated tissue |
US5885697A (en) * | 1996-12-17 | 1999-03-23 | Kimberly-Clark Worldwide, Inc. | Soft treated tissue |
US6576575B2 (en) | 2000-05-15 | 2003-06-10 | Kimberly-Clark Worldwide, Inc. | Dispersible adherent article |
JP2006016733A (en) * | 2004-07-02 | 2006-01-19 | Daio Paper Corp | Water-disaggregative article |
EP1630288A1 (en) * | 2004-08-20 | 2006-03-01 | Kao Corporation | Bulky water-disintegratable cleaning article and process of producing water-disintegratable paper |
WO2016208625A1 (en) * | 2015-06-25 | 2016-12-29 | 株式会社クラレ | Readily fibrillatable polyvinyl alcohol fiber and method for manufacturing same |
KR20170131344A (en) | 2015-03-31 | 2017-11-29 | 다이오 페이퍼 코퍼레이션 | Tissue paper |
KR20170131345A (en) | 2015-03-31 | 2017-11-29 | 다이오 페이퍼 코퍼레이션 | Tissue paper |
KR20180061185A (en) | 2015-09-28 | 2018-06-07 | 다이오 페이퍼 코퍼레이션 | Tissue paper |
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JPS59144426A (en) * | 1983-02-04 | 1984-08-18 | ピジヨン株式会社 | Washable wiping paper |
JPS6340555A (en) * | 1986-08-06 | 1988-02-20 | 小林製薬株式会社 | Tissue paper for toilet seat |
-
1988
- 1988-09-06 JP JP63224099A patent/JP2604436B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS59144426A (en) * | 1983-02-04 | 1984-08-18 | ピジヨン株式会社 | Washable wiping paper |
JPS6340555A (en) * | 1986-08-06 | 1988-02-20 | 小林製薬株式会社 | Tissue paper for toilet seat |
Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5558873A (en) * | 1994-06-21 | 1996-09-24 | Kimberly-Clark Corporation | Soft tissue containing glycerin and quaternary ammonium compounds |
US5601871A (en) * | 1995-02-06 | 1997-02-11 | Krzysik; Duane G. | Soft treated uncreped throughdried tissue |
US5614293A (en) * | 1995-02-06 | 1997-03-25 | Kimberly-Clark Corporation | Soft treated uncreped throughdried tissue |
US5650218A (en) * | 1995-02-06 | 1997-07-22 | Kimberly-Clark Corporation | Soft treated tissue |
US5665426A (en) * | 1995-02-06 | 1997-09-09 | Kimberly-Clark Corporation | Soft treated tissue |
WO1997013920A1 (en) * | 1995-10-13 | 1997-04-17 | Uni-Charm Corporation | Biodegradable and hydrolyzable sheet |
US5905046A (en) * | 1995-10-13 | 1999-05-18 | Uni-Charm Corporation | Biodegradable and hydrolyzable sheet |
US5885697A (en) * | 1996-12-17 | 1999-03-23 | Kimberly-Clark Worldwide, Inc. | Soft treated tissue |
US6576575B2 (en) | 2000-05-15 | 2003-06-10 | Kimberly-Clark Worldwide, Inc. | Dispersible adherent article |
JP4746286B2 (en) * | 2004-07-02 | 2011-08-10 | 大王製紙株式会社 | Water-degradable article |
JP2006016733A (en) * | 2004-07-02 | 2006-01-19 | Daio Paper Corp | Water-disaggregative article |
EP1630288A1 (en) * | 2004-08-20 | 2006-03-01 | Kao Corporation | Bulky water-disintegratable cleaning article and process of producing water-disintegratable paper |
US7758724B2 (en) | 2004-08-20 | 2010-07-20 | Kao Corporation | Bulky water-disintegratable cleaning article and process for producing water-disintegratable paper |
KR20170131344A (en) | 2015-03-31 | 2017-11-29 | 다이오 페이퍼 코퍼레이션 | Tissue paper |
KR20170131345A (en) | 2015-03-31 | 2017-11-29 | 다이오 페이퍼 코퍼레이션 | Tissue paper |
US10316470B2 (en) | 2015-03-31 | 2019-06-11 | Daio Paper Corporation | Tissue paper |
US11519133B2 (en) | 2015-03-31 | 2022-12-06 | Daio Paper Corporation | Tissue paper |
WO2016208625A1 (en) * | 2015-06-25 | 2016-12-29 | 株式会社クラレ | Readily fibrillatable polyvinyl alcohol fiber and method for manufacturing same |
US11053610B2 (en) | 2015-06-25 | 2021-07-06 | Kuraray Co., Ltd. | Readily fibrillative polyvinyl alcohol fiber and method for manufacturing same |
KR20180061185A (en) | 2015-09-28 | 2018-06-07 | 다이오 페이퍼 코퍼레이션 | Tissue paper |
US10618261B2 (en) | 2015-09-28 | 2020-04-14 | Daio Paper Corporation | Tissue paper |
Also Published As
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JP2604436B2 (en) | 1997-04-30 |
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