CN103459695B - The excellent non-woven fabrics of heat endurance, flexibility - Google Patents
The excellent non-woven fabrics of heat endurance, flexibility Download PDFInfo
- Publication number
- CN103459695B CN103459695B CN201180069808.XA CN201180069808A CN103459695B CN 103459695 B CN103459695 B CN 103459695B CN 201180069808 A CN201180069808 A CN 201180069808A CN 103459695 B CN103459695 B CN 103459695B
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- China
- Prior art keywords
- nonwoven fabric
- long
- fiber
- fibers
- polyolefin
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- 239000004745 nonwoven fabric Substances 0.000 title claims abstract description 106
- 239000000835 fiber Substances 0.000 claims abstract description 102
- 239000000463 material Substances 0.000 claims abstract description 27
- 229920000098 polyolefin Polymers 0.000 claims abstract description 22
- 238000005452 bending Methods 0.000 claims abstract description 14
- -1 polypropylene Polymers 0.000 claims description 37
- 238000012360 testing method Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000004743 Polypropylene Substances 0.000 claims description 9
- 229920001155 polypropylene Polymers 0.000 claims description 9
- 238000009835 boiling Methods 0.000 claims description 8
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- 239000010935 stainless steel Substances 0.000 claims description 5
- 238000005259 measurement Methods 0.000 claims description 4
- 206010021639 Incontinence Diseases 0.000 claims description 3
- 230000002745 absorbent Effects 0.000 abstract description 4
- 239000002250 absorbent Substances 0.000 abstract description 4
- 238000000034 method Methods 0.000 description 27
- 239000003795 chemical substances by application Substances 0.000 description 13
- 230000037303 wrinkles Effects 0.000 description 13
- 238000012545 processing Methods 0.000 description 12
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000009987 spinning Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 238000007789 sealing Methods 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000004049 embossing Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000007757 hot melt coating Methods 0.000 description 3
- 239000012943 hotmelt Substances 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XMHIUKTWLZUKEX-UHFFFAOYSA-N hexacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O XMHIUKTWLZUKEX-UHFFFAOYSA-N 0.000 description 2
- 238000007602 hot air drying Methods 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- LKOVPWSSZFDYPG-WUKNDPDISA-N trans-octadec-2-enoic acid Chemical compound CCCCCCCCCCCCCCC\C=C\C(O)=O LKOVPWSSZFDYPG-WUKNDPDISA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- ATNNLHXCRAAGJS-QZQOTICOSA-N (e)-docos-2-enoic acid Chemical compound CCCCCCCCCCCCCCCCCCC\C=C\C(O)=O ATNNLHXCRAAGJS-QZQOTICOSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-Hydroxyoctadecanoic acid Natural products CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- IZLFHMOZOWMKBO-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;propane-1,2,3-triol Chemical compound OCC(O)CO.OCC(O)CO.CCC(CO)(CO)CO IZLFHMOZOWMKBO-UHFFFAOYSA-N 0.000 description 1
- ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 description 1
- LXKCZUOSRQSRHW-UHFFFAOYSA-N 6-hydroxyoctadecanoic acid Chemical compound CCCCCCCCCCCCC(O)CCCCC(O)=O LXKCZUOSRQSRHW-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002961 polybutylene succinate Polymers 0.000 description 1
- 239000004631 polybutylene succinate Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4282—Addition polymers
- D04H1/4291—Olefin series
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers of the pads
- A61F13/511—Topsheet, i.e. the permeable cover or layer facing the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/15—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
- A61F13/51—Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators characterised by the outer layers of the pads
- A61F13/514—Backsheet, i.e. the impermeable cover or layer furthest from the skin
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/005—Synthetic yarns or filaments
- D04H3/007—Addition polymers
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
- D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Biomedical Technology (AREA)
- Public Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Nonwoven Fabrics (AREA)
- Absorbent Articles And Supports Therefor (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
- Laminated Bodies (AREA)
Abstract
Description
技术领域technical field
本发明涉及适合于在卫生材料中使用的吸收性物品的顶层片材(top sheet)、底层片材(back sheet)或侧面收集部的、加工性优异的由聚烯烃系纤维形成的无纺布。The present invention relates to a non-woven fabric formed of polyolefin-based fibers which is excellent in processability and is suitable for a top sheet, a back sheet, or a side collection part of an absorbent article used as a hygienic material .
背景技术Background technique
近年来,一次性尿布的普及是显著的,其产量也逐渐激增。作为这种环境下的一次性尿布,减少其生产线上的损失和品质的稳定性是重要的。在尿布生产线中,作为原材料的无纺布的热稳定性低时,在与薄膜贴合的工序中产生无纺布的宽度尺寸变化,发生褶皱产生、弯曲等各种不良情况。进而,在热封工序中由于热封辊的热的影响,无纺布自身收缩变形,发生褶皱产生、弯曲,因此需要热稳定性高的无纺布。In recent years, the popularity of disposable diapers has been remarkable, and its production has gradually surged. As a disposable diaper in this environment, it is important to reduce the loss on the production line and to stabilize the quality. In a diaper production line, if the thermal stability of the nonwoven fabric used as a raw material is low, the width dimension of the nonwoven fabric will change during the lamination process with the film, and various problems such as wrinkles and bending will occur. Furthermore, in the heat-sealing process, the non-woven fabric itself shrinks and deforms due to the influence of heat from the heat-sealing roll, causing wrinkles and bending. Therefore, a non-woven fabric with high thermal stability is required.
一直以来,作为使无纺布的热稳定性良好的手段,使用通过提高热粘接温度的方法、提高粘结压力的方法、提高压纹面积率的方法等来提高无纺布的纤维的粘接水平从而抑制尺寸变化的方法等,但使用其中任意方法都会提高粘接水平,从而使无纺布的质地变硬。即,现有的使无纺布的热稳定性良好的手段存在如下的问题:对用于卫生材料而言,柔软性差,兼具无纺布的柔软性和热稳定性是非常困难的。Conventionally, as a means of improving the thermal stability of nonwoven fabrics, methods such as increasing the thermal bonding temperature, increasing the bonding pressure, increasing the embossing area ratio, etc. are used to increase the bonding strength of the fibers of the nonwoven fabric. However, using any of these methods will increase the level of adhesion, thereby making the texture of the nonwoven fabric harder. That is, conventional methods for improving the thermal stability of nonwoven fabrics have the following problems: they are poor in flexibility when used in hygienic materials, and it is very difficult to achieve both flexibility and thermal stability of nonwoven fabrics.
以下的专利文献1中记载了:使用丙烯·乙烯无规共聚物,为了兼具柔软性和热稳定性,将乙烯含量设为特定的狭窄范围。由此,在专利文献1所记载的发明中,利用极其限定性的原料制造无纺布。The following Patent Document 1 describes that a propylene/ethylene random copolymer is used, and the ethylene content is set within a specific narrow range in order to achieve both flexibility and thermal stability. Thus, in the invention described in Patent Document 1, a nonwoven fabric is produced using extremely limited raw materials.
另外,以下的专利文献2中记载了提高热粘接温度来降低热收缩率的方法。然而,专利文献2所记载的方法中,无纺布的质地变硬,对用于卫生材料而言是不优选的。In addition, the following Patent Document 2 describes a method of increasing the thermal bonding temperature to reduce the thermal shrinkage rate. However, in the method described in patent document 2, the texture of a nonwoven fabric becomes hard, and it is not preferable to use it for a sanitary material.
现有技术文献prior art literature
专利文献patent documents
专利文献1:日本特开平10-96157号公报Patent Document 1: Japanese Patent Application Laid-Open No. 10-96157
专利文献2:日本特开2003-129364号公报Patent Document 2: Japanese Patent Laid-Open No. 2003-129364
发明内容Contents of the invention
发明要解决的问题The problem to be solved by the invention
本发明希望解决的问题是提供适合于在卫生材料中使用的吸收性物品的顶层片材、底层片材或侧面收集部且热稳定性高、柔软性优异、而且加工性也良好的无纺布。The problem to be solved by the present invention is to provide a nonwoven fabric suitable for the top sheet, back sheet or side collection part of absorbent articles used in hygienic materials, having high thermal stability, excellent flexibility, and good processability .
用于解决问题的方案solutions to problems
本发明人等为了解决前述问题而反复进行了深入研究和实验,结果发现,通过将构成无纺布的聚烯烃系纤维的微晶尺寸设为特定的尺寸,将无纺布的弯曲柔软度设定为特定范围,能够抑制在卫生材料加工工序中的薄膜贴合工序中由涂布热熔剂时的热的影响导致的宽度尺寸变化、褶皱的产生、无纺布的弯曲等,进而,还能够抑制在作为后续工序的热封工序中的由热封辊的热的影响导致的宽度尺寸变化、褶皱的产生、无纺布的弯曲等,从而完成了本发明。The inventors of the present invention conducted intensive studies and experiments in order to solve the aforementioned problems. As a result, they found that by setting the crystallite size of the polyolefin-based fibers constituting the nonwoven fabric to a specific size, the bending softness of the nonwoven fabric can be set to a certain level. In a specific range, it is possible to suppress changes in the width dimension, generation of wrinkles, and bending of the nonwoven fabric caused by the influence of heat when applying the hot melt agent in the film bonding process in the sanitary material processing process. The present invention has been accomplished by suppressing changes in width dimensions, generation of wrinkles, warping of the nonwoven fabric, etc. due to the influence of heat of the heat-sealing roll in the heat-sealing process as a subsequent process.
另外,本发明人等发现,通过在无纺布的生产工序中将牵引装置入口的纤维温度和牵引空气风速设定为规定范围,微晶尺寸会处于特定范围,由此,可得到热稳定性高、柔软性优异、而且加工性也良好且可以适用于卫生材料的无纺布,从而达成了本发明。In addition, the inventors of the present invention have found that by setting the fiber temperature at the inlet of the pulling device and the wind speed of the pulling air to a predetermined range in the production process of the nonwoven fabric, the crystallite size will be in a specific range, thereby achieving thermal stability. The present invention has been achieved by a nonwoven fabric that is high, excellent in softness, and has good processability and can be applied to hygienic materials.
即,本发明如下所述。That is, the present invention is as follows.
一种无纺布,其特征在于,其由聚烯烃系纤维形成,该聚烯烃系纤维的微晶尺寸为15nm以上且50nm以下,并且该无纺布的弯曲柔软度为5mm以上且100mm以下。A nonwoven fabric characterized in that it is formed of polyolefin fibers, the crystallite size of the polyolefin fibers is not less than 15 nm and not more than 50 nm, and the bending softness of the nonwoven fabric is not less than 5 mm and not more than 100 mm.
根据前述[1]所述的无纺布,其中,前述无纺布的沸水收缩率为0%以上且3.0%以下。The nonwoven fabric according to the above [1], wherein the boiling water shrinkage of the nonwoven fabric is not less than 0% and not more than 3.0%.
根据前述[1]或[2]所述的无纺布,其中,前述聚烯烃系纤维为聚丙烯系纤维。The nonwoven fabric according to [1] or [2] above, wherein the polyolefin-based fibers are polypropylene-based fibers.
根据前述[1]~[3]中任一项所述的无纺布,其中,前述无纺布为长纤维无纺布。The nonwoven fabric according to any one of [1] to [3], wherein the nonwoven fabric is a long-fiber nonwoven fabric.
根据前述[1]~[4]中任一项所述的无纺布,其中,前述聚烯烃系纤维的平均单纱纤度为0.5dtex以上且3.5dtex以下。The nonwoven fabric according to any one of [1] to [4] above, wherein the polyolefin-based fibers have an average single-yarn fineness of 0.5 dtex to 3.5 dtex.
根据前述[1]~[5]中任一项所述的无纺布,其中,前述无纺布在120℃下的干热收缩率为0%以上且5.0%以下。The nonwoven fabric according to any one of [1] to [5] above, wherein the dry heat shrinkage rate of the nonwoven fabric at 120° C. is 0% or more and 5.0% or less.
一种卫生材料,其是使用前述[1]~[6]中任一项所述的无纺布而形成的。A hygienic material formed using the nonwoven fabric according to any one of [1] to [6].
根据前述[7]所述的卫生材料,其为一次性尿布、卫生巾或失禁垫的形态。The hygienic material according to the above [7], which is in the form of a disposable diaper, a sanitary napkin or an incontinence pad.
发明的效果The effect of the invention
本发明的无纺布是由聚烯烃系纤维形成的无纺布,将聚烯烃系纤维的微晶尺寸设为15nm以上且50nm以下,将弯曲柔软度设为5mm以上且100mm以下,从而保持柔软性,而且加工性也良好。The non-woven fabric of the present invention is a non-woven fabric formed of polyolefin-based fibers, and the crystallite size of the polyolefin-based fibers is 15 nm to 50 nm, and the bending flexibility is 5 mm to 100 mm, so as to maintain flexibility properties, and good processability.
为了抑制加工时由热导致的褶皱的产生、弯曲,将微晶尺寸设为某一尺寸以上是重要的。例如,即使结晶度相同,小尺寸的晶体大量存在时,纤维整体也会发生收缩。另一方面,微晶尺寸大时,结晶部刚性地抑制分子的运动,能够抑制收缩。In order to suppress generation of wrinkles and warping due to heat during processing, it is important to make the crystallite size larger than a certain size. For example, even if the degree of crystallinity is the same, if a large number of small-sized crystals exist, the entire fiber shrinks. On the other hand, when the crystallite size is large, the crystal part rigidly suppresses molecular movement, and shrinkage can be suppressed.
进而,为了使加工性(加工适性)良好,需要适度的柔软性。柔软性过低时,无法追随加工时的张力变动、辊圆周速度变动等,出现褶皱产生、曲折移动等问题。Furthermore, in order to make processability (processing suitability) favorable, moderate flexibility is required. When the softness is too low, it is impossible to follow the fluctuations in tension during processing, the fluctuations in the peripheral speed of the roll, etc., and problems such as wrinkles and zigzagging occur.
本发明的无纺布由于具有前述构成,因此适合于在卫生材料中使用的吸收性物品的顶层片材、底层片材或侧面收集部,加工性优异。Since the nonwoven fabric of the present invention has the aforementioned constitution, it is suitable for a top sheet, a back sheet, or a side collecting portion of an absorbent article used in hygienic materials, and has excellent processability.
附图说明Description of drawings
图1是说明弯曲柔软度的测定方法的示意图。FIG. 1 is a schematic diagram illustrating a method of measuring bending softness.
具体实施方式detailed description
以下对本发明进行详细描述。The present invention is described in detail below.
作为构成本发明的无纺布的聚烯烃系纤维,例如可列举出由聚乙烯、聚丙烯、这些单体与其它α-烯烃的共聚物等树脂形成的纤维。其中,从强度强、使用时不易断裂、且生产卫生材料时的尺寸稳定性优异出发,优选使用聚丙烯纤维。聚丙烯可以是利用通常的齐格勒-纳塔(Ziegler-Natta)催化剂合成的聚合物,也可以是利用以金属茂为代表的单位点活性催化剂合成的聚合物。另外,可以是乙烯无规共聚聚丙烯,乙烯含量不足2%、优选不足1%是优选的。作为其它α-烯烃,为碳数3~10的烯烃,具体而言,可列举出丙烯、1-丁烯、1-戊烯、1-己烯、4-甲基-1-戊烯、1-辛烯等。它们可以单独使用一种,也可以组合两种以上使用。或者,也可以将聚烯烃系纤维、聚对苯二甲酸乙二醇酯纤维、聚对苯二甲酸丁二醇酯纤维、聚萘二甲酸乙二醇酯纤维、共聚聚酯等聚酯系纤维、尼龙-6纤维、尼龙-66纤维、共聚尼龙等聚酰胺系纤维、聚乳酸、聚丁二酸丁二醇酯、聚丁二酸乙二醇酯等生物降解性纤维使用一种或组合两种以上来使用。优选的是,单独使用一种即可。进而,以聚烯烃系树脂为表面层的芯鞘纤维也可。另外,其纤维形状不仅可以为通常的圆形纤维,也可以是卷曲纤维、异形纤维等特殊形态的纤维。Examples of the polyolefin-based fibers constituting the nonwoven fabric of the present invention include fibers made of resins such as polyethylene, polypropylene, and copolymers of these monomers and other α-olefins. Among them, polypropylene fibers are preferably used because they have high strength, are not easily broken during use, and are excellent in dimensional stability when producing hygienic materials. Polypropylene may be a polymer synthesized using a general Ziegler-Natta catalyst, or a polymer synthesized using a single-site active catalyst represented by a metallocene. Alternatively, ethylene random copolymerized polypropylene may be used, and the ethylene content is preferably less than 2%, preferably less than 1%. Other α-olefins are olefins having 3 to 10 carbon atoms, specifically, propylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1 -octene etc. These may be used alone or in combination of two or more. Alternatively, polyester fibers such as polyolefin fibers, polyethylene terephthalate fibers, polybutylene terephthalate fibers, polyethylene naphthalate fibers, and copolyesters may be used , Nylon-6 fiber, Nylon-66 fiber, polyamide fibers such as copolymerized nylon, polylactic acid, polybutylene succinate, polyethylene succinate and other biodegradable fibers use one or a combination of two Use more than one species. It is preferable to use only one kind. Furthermore, a core-sheath fiber having a polyolefin-based resin as a surface layer may also be used. In addition, the fiber shape may be not only ordinary round fibers, but also fibers of special forms such as crimped fibers and special-shaped fibers.
从强度/尺寸稳定性的观点出发,特别优选以均聚聚丙烯为主成分。From the standpoint of strength and dimensional stability, it is particularly preferable to use homopolypropylene as the main component.
另外,在聚丙烯的情况下,作为MFR,下限为20g/10分钟以上、优选超过30g/10分钟、更优选超过40g/10分钟、进一步优选超过53g/10分钟。上限为100g/10分钟以下、优选为85g/10分钟以下、更优选为70g/10分钟以下、进一步优选不足65g/10分钟。MFR处于该范围内时,树脂的流动性良好,可得到弯曲柔软度良好的无纺布。MFR是按照JIS-K7210“塑料-热塑性塑料的熔体质量流动速率(MFR)和熔体体积流动速率(MVR)的试验方法”的表1、试验温度230℃、试验载荷2.16kg进行测定而求出的。In addition, in the case of polypropylene, the lower limit of the MFR is 20 g/10 minutes or more, preferably more than 30 g/10 minutes, more preferably more than 40 g/10 minutes, and still more preferably more than 53 g/10 minutes. The upper limit is 100 g/10 minutes or less, preferably 85 g/10 minutes or less, more preferably 70 g/10 minutes or less, still more preferably less than 65 g/10 minutes. When the MFR is within this range, the fluidity of the resin is good, and a nonwoven fabric with good bending flexibility can be obtained. MFR is calculated according to Table 1 of JIS-K7210 "Melt Mass Flow Rate (MFR) and Melt Volume Flow Rate (MVR) Test Methods of Plastics - Thermoplastics", the test temperature is 230°C, and the test load is 2.16kg. out.
构成本发明的无纺布的聚烯烃系纤维中还可以配混成核剂、阻燃剂、无机填充剂、颜料、着色剂、耐热稳定剂、抗静电剂等。A nucleating agent, a flame retardant, an inorganic filler, a pigment, a colorant, a heat-resistant stabilizer, an antistatic agent, etc. may be compounded with the polyolefin fiber which comprises the nonwoven fabric of this invention.
作为将聚烯烃系纤维接合来制造无纺布时的接合手段,可列举出部分热压接法、热风法、利用熔融成分的接合(热熔剂)法、其它各种方法,从强度的观点出发,优选部分热压接法。As the bonding means when polyolefin-based fibers are bonded to produce non-woven fabrics, partial thermocompression bonding, hot air method, bonding (hot melt) method using molten components, and various other methods can be mentioned. From the viewpoint of strength , preferably partial thermocompression bonding.
本发明的无纺布的部分热压接的热压接面积率从强度保持和柔软性的观点出发,为3%以上且40%以下、优选为4%以上且25%以下、更优选为4%以上且20%以下、进一步优选为5%以上且15%以下。The thermocompression bonded area ratio of the nonwoven fabric of the present invention is from the viewpoint of strength retention and softness to 3% to 40%, preferably 4% to 25%, more preferably 4%. % or more and 20% or less, more preferably 5% or more and 15% or less.
另外,本发明的部分热压接处理可以通过超声波法进行、或者使纤维网(web)穿过加热压纹辊间来进行,由此使其表背一体化,例如,针尖状、椭圆形、菱形、矩形等凹凸图案散布于无纺布整面。从生产率的观点出发,优选使用加热压纹辊。In addition, part of the thermocompression bonding treatment of the present invention can be performed by ultrasonic method, or by passing the web (web) through heated embossing rollers, thereby integrating the front and back, for example, needle-shaped, oval, Concave-convex patterns such as diamonds and rectangles are scattered on the entire surface of the non-woven fabric. From the viewpoint of productivity, it is preferable to use a heated embossing roll.
构成本发明的无纺布的聚烯烃系纤维的平均单纱纤度优选为0.5dtex以上且3.5dtex以下、更优选为0.7dtex以上且3.2dtex以下、进一步优选为0.9dtex以上且2.8dtex以下。从纺丝稳定性的观点出发,优选为0.5dtex以上,纤度越细,制成无纺布时丝的粘接点越多,因此强度高,柔软性良好。由于其主要用于卫生材料,因此,从无纺布的强度的观点出发,优选为3.5dtex以下。The average single yarn fineness of the polyolefin fibers constituting the nonwoven fabric of the present invention is preferably from 0.5 dtex to 3.5 dtex, more preferably from 0.7 dtex to 3.2 dtex, still more preferably from 0.9 dtex to 2.8 dtex. From the viewpoint of spinning stability, it is preferably 0.5 dtex or more. The finer the fineness, the more bonding points of filaments when made into a nonwoven fabric, so the strength is high and the flexibility is good. Since it is mainly used for sanitary materials, it is preferably 3.5 dtex or less from the viewpoint of the strength of the nonwoven fabric.
本发明的无纺布的单位面积重量为8g/m2以上且40g/m2以下、优选为10g/m2以上且30g/m2以下、更优选为10g/m2以上且25g/m2以下、进一步优选为10g/m2以上且不足23g/m2。为8g/m2以上时,满足用于卫生材料的无纺布所需的强度的需求,另一方面,为40g/m2以下时,满足用于卫生材料的无纺布的柔软性,在外观上给人留下看似较厚的印象。The basis weight of the nonwoven fabric of the present invention is 8 g/m 2 to 40 g/m 2 , preferably 10 g/m 2 to 30 g/m 2 , more preferably 10 g/m 2 to 25 g/m 2 Below, more preferably 10 g/m 2 or more and less than 23 g/m 2 . When it is 8g/m 2 or more, it meets the demand for the strength required for non-woven fabrics used in sanitary materials. On the other hand, when it is 40g/m 2 or less, it meets the softness of non-woven fabrics used in sanitary materials. It gives the impression of being thicker in appearance.
本发明的无纺布的微晶尺寸为15nm以上且50nm以下、优选超过20nm且为50nm以下、更优选为25nm以上且40nm以下。微晶尺寸为15nm以上时,热稳定性良好,从用于卫生材料的无纺布的柔软性的观点出发,微晶尺寸为50nm以下。The nonwoven fabric of the present invention has a crystallite size of 15 nm to 50 nm, preferably more than 20 nm and 50 nm, more preferably 25 nm to 40 nm. When the crystallite size is 15 nm or more, thermal stability is good, and from the viewpoint of the flexibility of a nonwoven fabric used for sanitary materials, the crystallite size is 50 nm or less.
本发明的无纺布通过在将牵引装置入口的纤维温度设为30℃以上、牵引空气风速设为5000m/min以上的条件下用强力的牵引力进行牵引而使纤维细化,从而具有期望的微晶尺寸。纤维温度优选为30℃以上且80℃以下、更优选为35℃以上且70℃以下。牵引空气风速优选为6000m/min以上且30000m/min以下、更优选为7000m/min以上且20000m/min以下。通过将牵引装置入口的纤维温度和牵引空气风速设为该范围,能够制成规定的微晶尺寸,卫生材料的加工性良好。The nonwoven fabric of the present invention has a desired fineness by pulling with a strong pulling force under the conditions that the fiber temperature at the inlet of the pulling device is set to be 30° C. or higher and the wind speed of the pulling air is set to be 5000 m/min or higher. crystal size. The fiber temperature is preferably 30°C to 80°C, more preferably 35°C to 70°C. The wind speed of the draft air is preferably not less than 6000 m/min and not more than 30000 m/min, more preferably not less than 7000 m/min and not more than 20000 m/min. By setting the fiber temperature at the inlet of the drawing device and the wind speed of the drawing air within these ranges, a predetermined crystallite size can be obtained, and the workability of the hygienic material is improved.
另外,对本发明的无纺布的牵引方法没有特别限制,为了得到微晶尺寸大且热稳定性优异的无纺布,使用基于空气喷射的高速气流牵引装置的方法是较好的,使用矩形型的牵引装置是更良好的。In addition, the drawing method of the nonwoven fabric of the present invention is not particularly limited. In order to obtain a nonwoven fabric with a large crystallite size and excellent thermal stability, it is better to use a high-speed airflow drawing device based on air jets. The traction device is better.
以下定义的本发明的无纺布的纵向和横向的平均“弯曲柔软度”为5mm以上且100mm以下、优选为5mm以上且90mm以下、更优选为10mm以上且80mm以下。弯曲柔软度为该范围时,成为加工性优异且质地、柔软性优异的无纺布。The average "bending softness" of the nonwoven fabric of the present invention defined below in the longitudinal and transverse directions is not less than 5 mm and not more than 100 mm, preferably not less than 5 mm and not more than 90 mm, more preferably not less than 10 mm and not more than 80 mm. When the flexural softness is within this range, it becomes a nonwoven fabric having excellent processability, texture, and flexibility.
关于本发明的无纺布的沸水收缩率,由于热水包围纤维的周围,因此能够效率良好地传播热能,对于观察纤维的热稳定性而言是适宜的手法。本发明的沸水收缩率优选为0%以上且3.0%以下、更优选为0.1%以上且2.0%以下、进一步优选为0.1%以上且1.0%以下。沸水收缩率为该范围时,在卫生材料的生产线中由涂布热熔剂时、热封时的热导致的缩幅、褶皱产生受到抑制,能够稳定地加工而不会断裂。Regarding the boiling water shrinkage of the nonwoven fabric of the present invention, since hot water surrounds the fiber, thermal energy can be efficiently transmitted, and it is an appropriate method for observing the thermal stability of the fiber. The shrinkage in boiling water in the present invention is preferably 0% to 3.0%, more preferably 0.1% to 2.0%, and still more preferably 0.1% to 1.0%. When the boiling water shrinkage ratio is within this range, shrinkage and wrinkles caused by heat during hot melt coating and heat sealing are suppressed in the production line of sanitary materials, and stable processing can be performed without breaking.
本发明的无纺布的干热收缩率在120℃下优选为0%以上且5.0%以下、更优选为0.1%以上且3.0%以下、进一步优选为0.2%以上且1.5%以下。干热收缩率为该范围时,在卫生材料的生产线中由涂布热熔剂时、热封时的热导致的缩幅、褶皱产生受到抑制,能够稳定地加工而不会断裂。The dry heat shrinkage rate of the nonwoven fabric of the present invention is preferably 0% to 5.0% at 120°C, more preferably 0.1% to 3.0%, still more preferably 0.2% to 1.5%. When the dry heat shrinkage ratio is within this range, shrinkage and wrinkle generation due to heat during hot melt coating and heat sealing are suppressed in a hygienic material production line, and stable processing without breakage is possible.
本发明的无纺布中还可以应用亲水剂。作为所述亲水剂,考虑到对人体的安全性、工序中的安全性等,优选单独或以混合物的形式使用对高级醇、高级脂肪酸、烷基酚等加成环氧乙烷而得到的非离子系活性剂、烷基磷酸盐、烷基硫酸盐等阴离子系活性剂等。Hydrophilic agents can also be used in the nonwoven fabric of the present invention. As the hydrophilic agent, in consideration of safety to the human body, safety in the process, etc., it is preferable to use one obtained by adding ethylene oxide to a higher alcohol, a higher fatty acid, an alkylphenol, etc. alone or in a mixture. Nonionic active agents, anionic active agents such as alkyl phosphates and alkyl sulfates, etc.
亲水剂的附着量根据所需的性能而不同,通常相对于纤维优选为0.1重量%以上且1.0重量%以下的范围,更优选为0.15重量%以上且0.8重量%以下、进一步优选为0.2重量%以上且0.6重量%以下。附着量处于该范围内时,满足作为卫生材料的顶层片材的亲水性能,加工性也良好。The amount of the hydrophilic agent attached varies depending on the desired performance, and is usually preferably in the range of 0.1% by weight to 1.0% by weight relative to the fiber, more preferably 0.15% by weight to 0.8% by weight, and still more preferably 0.2% by weight % or more and 0.6% by weight or less. When the adhesion amount is within this range, the hydrophilic performance of the top sheet as a hygienic material is satisfied, and the processability is also good.
作为涂布亲水剂的方法,通常,可以使用稀释了的亲水剂,采用浸渍法、喷雾法、涂覆(辊舐涂布、凹版涂布)法等现存的方法,优选将根据需要预先混合了的亲水剂用水等溶剂稀释后进行涂布。As a method of applying a hydrophilic agent, generally, a diluted hydrophilic agent can be used, and an existing method such as a dipping method, a spray method, or a coating (roll coating, gravure coating) method can be used. The mixed hydrophilic agent is diluted with a solvent such as water, and then applied.
将亲水剂用水等溶剂稀释后进行涂布时,有时需要干燥工序。作为此时的干燥方法,可以采用利用对流传热、传导传热、辐射传热等的已知方法,可以使用热风、利用红外线的干燥、利用热接触的干燥方法等。When the hydrophilizing agent is diluted with a solvent such as water and then applied, a drying step may be required. As the drying method at this time, known methods using convective heat transfer, conductive heat transfer, radiation heat transfer, etc. can be used, and hot air, drying using infrared rays, drying methods using thermal contact, etc. can be used.
本发明的无纺布中还可以应用软化剂。作为所述软化剂,优选酯化合物,更优选地,可列举出3~6元的多元醇与单羧酸的酯化合物。Softeners can also be used in the nonwoven fabric of the present invention. As said softening agent, ester compounds are preferable, and ester compounds of 3-6 valent polyhydric alcohols and a monocarboxylic acid are mentioned more preferably.
作为3~6元的多元醇,例如可列举出甘油、三羟甲基丙烷等3元的多元醇;季戊四醇、葡萄糖、脱水山梨糖醇、二甘油、乙二醇二甘油醚等4元的多元醇;三甘油、三羟甲基丙烷二甘油醚等5元的多元醇;山梨糖醇、四甘油、二季戊四醇等6元的多元醇等。Examples of 3- to 6-valent polyhydric alcohols include trivalent polyhydric alcohols such as glycerin and trimethylolpropane; Alcohol; triglycerin, trimethylolpropane diglycerol and other 5-membered polyols; sorbitol, tetraglycerin, dipentaerythritol and other 6-membered polyols, etc.
作为单羧酸,例如可列举出辛酸、十二烷酸、十四烷酸、十八烷酸、二十二烷酸、二十六烷酸、十八碳烯酸、二十二碳烯酸、异十八烷酸等单羧酸;环已烷羧酸等脂环式单羧酸;苯甲酸、甲基苯羧酸等芳香族单羧酸;羟基丙酸、羟基十八烷酸、羟基十八碳烯酸等羟基脂肪族单羧酸;烷基硫代丙酸等含硫脂肪族单羧酸等。Examples of monocarboxylic acids include octanoic acid, dodecanoic acid, tetradecanoic acid, octadecanoic acid, behenic acid, hexacosanoic acid, octadecenoic acid, and docosenoic acid. , isosteardecanoic acid and other monocarboxylic acids; cyclohexane carboxylic acid and other alicyclic monocarboxylic acids; benzoic acid, methylbenzene carboxylic acid and other aromatic monocarboxylic acids; hydroxypropionic acid, hydroxyoctadecanoic acid, hydroxyl Hydroxy aliphatic monocarboxylic acids such as octadecenoic acid; sulfur-containing aliphatic monocarboxylic acids such as alkylthiopropionic acid, etc.
酯化合物并非必须为单一成分,也可以为两种以上的混合物,也可以为源自天然物的油脂类。其中,包含不饱和脂肪酸的酯化合物容易被氧化,在纺丝时容易氧化劣化,因此,优选饱和的脂肪族单羧酸或芳香族单羧酸。关于源自天然物的油脂类,由于与原料油相比无味且稳定,因此优选使用加氢的酯化合物。The ester compound does not have to be a single component, and may be a mixture of two or more types, or may be oils and fats derived from natural products. Among them, ester compounds containing unsaturated fatty acids are easily oxidized and are easily oxidized and deteriorated during spinning. Therefore, saturated aliphatic monocarboxylic acids or aromatic monocarboxylic acids are preferred. As oils and fats derived from natural products, hydrogenated ester compounds are preferably used because they are odorless and more stable than raw material oils.
作为酯化合物,优选单羧酸的分子量较大且亲油性高。由于亲油性高,酯化合物进入聚烯烃系纤维的非晶部,阻碍结晶化,非晶区域增加,因此弯曲柔软度变得更小。As the ester compound, monocarboxylic acid preferably has a large molecular weight and high lipophilicity. Since the lipophilicity is high, the ester compound enters the amorphous part of the polyolefin fiber, hinders crystallization, increases the amorphous region, and thus reduces the flexural flexibility.
为了得到所述效果,酯化合物的熔点优选为70℃以上,更优选为80℃以上且150℃以下。酯化合物的熔点宽而具有范围时,该熔点意味着平均的熔点。另外,酯化合物中还可以配混其它组合物,例如,熔点不足70℃的酯化合物、其它有机化合物。In order to obtain the above effect, the melting point of the ester compound is preferably 70°C or higher, more preferably 80°C or higher and 150°C or lower. When the melting point of an ester compound is broad and has a range, this melting point means an average melting point. In addition, other compositions such as ester compounds having a melting point of less than 70° C. and other organic compounds may be blended with the ester compound.
作为软化剂的酯化合物的含有率相对于聚烯烃系纤维,优选为0.3重量%以上且5.0重量%以下。关于酯化合物,即使少量添加,弯曲柔软度、滑动容易度也明显提高,即使增加含量,也未观察到与含量相符的性能的提高。因此,考虑到纺丝性和发烟性,优选为5.0重量%以下、更优选为0.5重量%以上且3.5重量%以下、进一步优选为0.5重量%以上且2.0重量%以下。The content of the ester compound as a softener is preferably not less than 0.3% by weight and not more than 5.0% by weight relative to the polyolefin-based fibers. With regard to the ester compound, even if it is added in a small amount, the bending flexibility and the ease of sliding are significantly improved, and even if the content is increased, no performance improvement corresponding to the content is observed. Therefore, in consideration of spinnability and smoke generation, it is preferably 5.0% by weight or less, more preferably 0.5% by weight or more and 3.5% by weight or less, further preferably 0.5% by weight or more and 2.0% by weight or less.
对本发明的无纺布的制造方法没有特别限定,由于主要用于卫生材料,因此,从强度的观点出发,优选纺粘(S)法,通过层叠成SS、SSS、SSSS,分散提高,故而更加优选。另外,根据目的,也可以将纺粘(S)纤维与熔喷(M)纤维层叠,可以为层叠成SM、SMS、SMMS、SMSMS的结构。The manufacturing method of the nonwoven fabric of the present invention is not particularly limited. Since it is mainly used for hygienic materials, the spunbond (S) method is preferred from the viewpoint of strength. By laminating into SS, SSS, and SSSS, the dispersion is improved, so it is more preferred. In addition, depending on the purpose, spunbond (S) fibers and meltblown (M) fibers may be laminated, and SM, SMS, SMMS, or SMSMS may be laminated.
本发明的纺丝温度为190℃以上且260℃以下、优选为200℃以上且255℃以下、更优选为205℃以上且230℃以下、进一步优选为210℃以上且225℃以下。纺丝温度为260℃以下时,由树脂分解物造成的喷丝头表面的沾污少,进而能够抑制由树脂的粘度降低而导致的断线的产生。另外,纺丝温度高时,制作的无纺布由于受到树脂分解物的影响,因此弯曲柔软度提高,显示出作为无纺布坚硬的倾向。纺丝温度为190℃以上时,能够抑制由树脂的粘度增高而导致的断线的产生,进而能够抑制由纺丝时的喷丝头内压力增高而导致的树脂泄漏等。The spinning temperature in the present invention is 190°C to 260°C, preferably 200°C to 255°C, more preferably 205°C to 230°C, further preferably 210°C to 225°C. When the spinning temperature is 260° C. or lower, the contamination of the spinneret surface by resin decomposition products is small, and the occurrence of thread breakage due to a decrease in the viscosity of the resin can be suppressed. In addition, when the spinning temperature is high, since the produced nonwoven fabric is affected by resin decomposition products, the bending softness is improved, and the nonwoven fabric tends to be hard as a nonwoven fabric. When the spinning temperature is 190° C. or higher, it is possible to suppress the occurrence of thread breakage due to an increase in the viscosity of the resin, and further suppress resin leakage due to an increase in the internal pressure of the spinneret during spinning.
本发明的无纺布根据目的可以是长纤维,也可以是短纤维,没有特别限定,由于主要用于卫生材料,因此从强度的观点出发,优选长纤维无纺布。The nonwoven fabric of the present invention may be long-fiber or short-fiber depending on the purpose, and is not particularly limited. Since it is mainly used for sanitary materials, long-fiber nonwoven fabric is preferable from the viewpoint of strength.
本发明的无纺布由于热稳定性非常高,因此可以适宜地用于卫生材料的制造,作为卫生材料,可列举出一次性尿布、卫生巾或失禁垫,可以适用于它们的表面的顶层片材、外侧的底层片材、底部周围的侧面收集部等。Since the nonwoven fabric of the present invention has very high thermal stability, it can be suitably used in the production of hygienic materials. Examples of hygienic materials include disposable diapers, sanitary napkins, and incontinence pads, and can be applied to top sheets on their surfaces. material, bottom sheet on the outside, side collectors around the bottom, etc.
另外,本发明的无纺布的用途不限定于前述用途,例如还可以用于面膜、暖手宝、胶带基布、防水片基布、外贴药基布、急救绷带基布、包装材料、擦拭制品、医用长袍、绷带、衣料、皮肤护理用薄片等。In addition, the use of the nonwoven fabric of the present invention is not limited to the aforementioned uses, for example, it can also be used for facial masks, hand warmers, adhesive tape base cloths, waterproof sheet base cloths, external medicine base cloths, first aid bandage base cloths, packaging materials, Wipes, medical gowns, bandages, clothing, sheets for skin care, etc.
实施例Example
以下,通过实施例和比较例具体说明本发明,但本发明不仅仅限定于下述实施例。Hereinafter, although an Example and a comparative example demonstrate this invention concretely, this invention is not limited only to a following example.
需要说明的是,实施例和比较例中使用的各种特性的评价方法如下所述,将得到的物性示于以下的表1。In addition, the evaluation methods of various characteristics used in the Example and the comparative example are as follows, and the obtained physical properties are shown in Table 1 below.
1.平均单纱纤度(dtex)1. Average single yarn denier (dtex)
除去制造的无纺布的两端10cm,在宽度方向上约5等分,采取1cm见方的试验片,用显微镜分别对各20点测定纤维的直径,由其平均值算出纤度。Remove 10 cm from both ends of the manufactured nonwoven fabric, divide it into about 5 equal parts in the width direction, take a 1 cm square test piece, measure the diameter of the fiber at 20 points each with a microscope, and calculate the fineness from the average value.
2.单位面积重量(g/m2)2. Weight per unit area (g/m 2 )
根据JIS-L1906、任意选取5片纵向20cm×横向5cm的试验片,测定质量,将其平均值换算为每单位面积的重量,从而求出。According to JIS-L1906, 5 test pieces of 20 cm in length x 5 cm in width were selected arbitrarily, the mass was measured, and the average value thereof was converted into weight per unit area to obtain it.
3.沸水收缩率(%)3. Boiling water shrinkage (%)
任意选取3片纵向25cm×横向25cm的试验片,在试样的纵向、横向各3处标记准确表示20cm的长度的记号。Randomly select 3 test pieces with a length of 25 cm x a width of 25 cm, and mark marks that accurately represent the length of 20 cm in each of the vertical and horizontal positions of the sample.
将试样在适当的容器中、在沸水中浸渍3分钟后,取出试样,用滤纸等轻轻吸除水,将一端用夹具夹住,在室温下悬吊,使其干燥。接着,测定最初标记的纵向、横向各3处的长度。通过以下的式子算出纵向的收缩率,求出平均值。After immersing the sample in boiling water for 3 minutes in a suitable container, take out the sample, gently absorb the water with filter paper, etc., clamp one end with a jig, hang it at room temperature, and make it dry. Next, the lengths of each of the longitudinal and transverse lengths of the first mark are measured at three places. The longitudinal contraction rate was calculated by the following formula, and the average value was calculated|required.
沸水收缩率(%)=(L-L’)/L×100Boiling water shrinkage (%)=(L-L’)/L×100
{式中,L:处理前的3条线的长度的总和(mm),此外,L’:处理后的3条线的长度的总和(mm)}。{wherein, L: the sum of the lengths of the three lines before processing (mm), and L': the sum of the lengths of the three lines after processing (mm)}.
4.干热收缩率(%)4. Dry heat shrinkage (%)
任意选取3片纵向25cm×横向25cm的试验片,对试样在纵向、横向各3处标记准确表示20cm的长度的记号。Randomly select 3 test pieces with a length of 25 cm x a width of 25 cm, and mark a mark that accurately represents the length of 20 cm on each of the vertical and horizontal positions of the sample.
将恒温干燥机设定为120℃,在干燥机中悬吊试样,干燥机的指示刻度达到规定的温度后,在干燥机内放置3分钟,取出并冷却至室温。接着,测定最初标记的纵向、横向各3处的长度。通过以下的式子算出纵向的收缩率,求出平均值。Set the constant temperature dryer to 120°C, hang the sample in the dryer, and when the indicating scale of the dryer reaches the specified temperature, place it in the dryer for 3 minutes, take it out and cool it to room temperature. Next, the lengths of each of the longitudinal and transverse lengths of the first mark are measured at three places. The longitudinal contraction rate was calculated by the following formula, and the average value was calculated|required.
干热收缩率(%)=(L-L’)/L×100Dry heat shrinkage (%)=(L-L’)/L×100
{式中,L:处理前的3条线的长度的总和(mm),此外,L’:处理后的3条线的长度的总和(mm)}。{In the formula, L: the sum of the lengths of the three lines before processing (mm), and L': the sum of the lengths of the three lines after processing (mm)}.
5.弯曲柔软度(mm)5. Bending softness (mm)
从无纺布试样中任意选取5片宽10cm、长30cm的试验片(以测定方向为30cm的方式选取试样),如图1所示地放置在平坦的工作台上,在试验片的中央部以与长度方向正交的方式载置不锈钢制的直尺。直尺优选宽度为2.5cm且测定标度为30cm(1)。接着,拿起试验片的一端,以不锈钢制的直尺为边界以在相反一侧的试验片上形成环而不形成折痕的状态慢慢重叠(2)。接着,将不锈钢制的直尺向折叠产生的环的方向、以与长度方向正交的状态慢慢滑动(3),将环由于试样的回弹力伸展而使折叠消失时的状态作为终点,以刻度读出试验片的端部与直尺间的距离(L)(4)。由表背的纵向和横向的n=5的各测定值的平均值算出弯曲柔软度。弯曲柔软度(mm)的值越小表示越柔软。Randomly select 5 test pieces with a width of 10 cm and a length of 30 cm from the non-woven fabric samples (select the sample with the measurement direction being 30 cm), and place them on a flat workbench as shown in Figure 1. A stainless steel ruler is placed in the center so as to be perpendicular to the longitudinal direction. The ruler preferably has a width of 2.5 cm and a measuring scale of 30 cm (1). Next, one end of the test piece was picked up, and the test piece on the opposite side was slowly overlapped with a stainless steel ruler as a boundary in a state where a loop was formed without creases (2). Next, slowly slide a stainless steel ruler in the direction of the folded ring in a state perpendicular to the longitudinal direction (3), and set the state where the fold disappears due to the stretching of the ring by the resilience of the sample as the end point, Read the distance (L) between the end of the test piece and the ruler with the scale (4). The flexural flexibility was calculated from the average value of n=5 measured values in the vertical and horizontal directions of the front and back. The smaller the value of the flexural softness (mm), the softer it is.
6.微晶尺寸(nm)6. Crystallite size (nm)
使用XRD分析仪[装置:Rigaku Corporation制造的NanoViewer,光学系统:针孔准直(共焦反射镜+第一狭缝:0.4mmφ+第二狭缝:0.3mmφ),X射线源:CuKα射线,45kV60mA,检测器:成像板,摄像头长度:80.8mm],将一根纤维放置于样品池,从纤维轴垂直方向入射X射线,检测透射散射(衍射)光。为了减小背景散射的影响,在第二狭缝的下游全部为真空、从第二狭缝至检测器间的X射线通路上没有试样以外的散射体的状态下进行测定。Using an XRD analyzer [apparatus: NanoViewer manufactured by Rigaku Corporation, optical system: pinhole collimation (confocal mirror + first slit: 0.4 mmφ + second slit: 0.3 mmφ), X-ray source: CuKα ray, 45kV60mA, detector: imaging plate, camera length: 80.8mm], place a fiber in the sample cell, inject X-rays from the direction perpendicular to the fiber axis, and detect the transmitted scattered (diffracted) light. In order to reduce the influence of background scatter, all the downstream of the second slit is vacuum, and the X-ray path from the second slit to the detector is free of scatterers other than the sample.
以测定时间10~12小时、由二维图案通过圆环平均求出一维WAXS曲线,进行峰分离,然后由源自(040)面的衍射峰宽度利用以下的式子算出与(040)面垂直的方向的微晶尺寸。With a measurement time of 10 to 12 hours, the one-dimensional WAXS curve is obtained from the two-dimensional pattern through the circular average, and the peaks are separated, and then the width of the diffraction peak originating from the (040) plane is calculated by the following formula. The crystallite size in the vertical direction.
[数学式1][mathematical formula 1]
{式中,K:谢乐常数(取决于微晶形状等的常数:使用0.9),λ:X射线波长、β:峰的半峰宽(半峰全宽:FWHM)(rad),此外,b:入射光束的发散的半峰宽(半峰全宽:FWHM)(rad)}。{In the formula, K: Scherrer constant (constant depending on the crystallite shape, etc.: use 0.9), λ: X-ray wavelength, β: peak width at half maximum (full width at half maximum: FWHM) (rad), and, b: Half width at half maximum (full width at half maximum: FWHM) (rad)} of divergence of the incident light beam.
7.由加工时的热导致的褶皱产生评价(加工性(加工适性))7. Evaluation of wrinkle generation due to heat during processing (processability (processing suitability))
对于宽30cm的无纺布试样,将在160℃下熔融了的聚烯烃系的热熔剂以线速度50m/min、利用本领域技术人员周知的通常的热熔涂布方法涂布到无纺布上。根据以下的评价基准评价涂布时的无纺布的褶皱的情况:For a non-woven fabric sample with a width of 30 cm, a polyolefin-based hot-melt agent melted at 160° C. was applied to the non-woven fabric at a line speed of 50 m/min by a common hot-melt coating method known to those skilled in the art. on cloth. The wrinkle of the nonwoven fabric at the time of coating was evaluated according to the following evaluation criteria:
◎:无褶皱产生◎: no wrinkles
○:线方向上产生褶皱,但可以涂覆○: Wrinkles occur in the line direction, but coating is possible
×:线方向上产生褶皱,不可涂覆×: Wrinkles are generated in the line direction and cannot be coated
[实施例1][Example 1]
将MFR为60g/10分钟(根据JIS-K7210、在温度230℃、载荷2.16kg下测定)的聚丙烯树脂通过纺粘法在喷嘴直径φ0.4mm、单孔喷出量0.56g/min·Hole、纺丝温度215℃的条件下挤出,对该长丝群使用基于空气喷射的高速气流牵引装置、在牵引装置入口的纤维温度为40℃、牵引空气风速为17500m/min的条件下进行牵引,朝向移动收集面挤出,制备平均单纱纤度1.1dtex的长纤维纤维网。A polypropylene resin with an MFR of 60g/10min (measured according to JIS-K7210 at a temperature of 230°C and a load of 2.16kg) is spunbonded through a nozzle diameter of φ0.4mm and a single hole discharge amount of 0.56g/min·Hole , Extrude under the condition of spinning temperature of 215°C, use a high-speed airflow traction device based on air jets for the filament group, draw under the conditions that the fiber temperature at the entrance of the traction device is 40°C, and the traction air speed is 17500m/min , and extrude towards the moving collection surface to prepare a long-fiber web with an average single yarn denier of 1.1 dtex.
接着,使得到的纤维网穿过平面辊与压纹辊(图案规格:直径0.425mm圆形,交错排列,横间距2.1mm,纵间距1.1mm,压接面积率6.3%)之间,在温度135℃和线性荷载35kgf/cm下将纤维彼此粘接,得到单位面积重量17g/m2的长纤维无纺布。Then, make the obtained fiber web pass between the flat roller and the embossing roller (pattern specification: diameter 0.425mm circle, staggered arrangement, horizontal spacing 2.1mm, vertical spacing 1.1mm, crimping area ratio 6.3%), at temperature The fibers were bonded to each other at 135°C and a linear load of 35 kgf/cm to obtain a long-fiber nonwoven fabric with a weight per unit area of 17 g/m 2 .
[实施例2][Example 2]
将牵引装置入口的纤维温度设为50℃、牵引空气风速设为15000m/min,与实施例1同样操作,得到平均单纱纤度1.5dtex、单位面积重量11g/m2的长纤维无纺布。The fiber temperature at the entrance of the traction device was set to 50°C, the draft air velocity was set to 15000m/min, and the same operation as in Example 1 was performed to obtain a long-fiber nonwoven fabric with an average single yarn fineness of 1.5dtex and a weight per unit area of 11g/m2.
[实施例3][Example 3]
将单孔喷出量设为0.90g/min·Hole、牵引装置入口的纤维温度设为65℃、牵引空气风速设为12500m/min,与实施例1同样操作,得到平均单纱纤度2.0dtex、单位面积重量25g/m2的长纤维无纺布。The single-hole ejection amount is set to 0.90g/min·Hole, the fiber temperature at the entrance of the traction device is set to 65°C, and the draft air velocity is set to 12500m/min, and the same operation as in Example 1 is performed to obtain an average single yarn denier of 2.0dtex, Long-fiber non - woven fabric with a weight per unit area of 25g/m2.
[实施例4][Example 4]
将MFR为60g/10分钟(根据JIS-K7210、在温度230℃、载荷2.16kg下测定)的聚丙烯树脂通过纺粘法、在喷嘴直径φ0.48mm、单孔喷出量0.33g/min·Hole、纺丝温度230℃的条件下挤出,对该长丝群通过冷风推压方式在牵引装置入口的纤维温度为40℃、牵引空气风速为6400m/min的条件下进行牵引,朝向移动收集面挤出,制备平均单纱纤度1.1dtex的长纤维纤维网。Polypropylene resin with an MFR of 60g/10min (measured according to JIS-K7210 at a temperature of 230°C and a load of 2.16kg) is spunbonded, with a nozzle diameter of φ0.48mm and a single-hole discharge rate of 0.33g/min· Hole, extruded at a spinning temperature of 230°C, the filament group is drawn by cold air pushing under the condition that the fiber temperature at the entrance of the pulling device is 40°C, and the wind speed of the pulling air is 6400m/min, and is collected towards the mobile Surface extrusion to prepare a long-fiber web with an average single yarn denier of 1.1 dtex.
接着,与实施例1同样地将纤维彼此粘接,得到单位面积重量17g/m2的长纤维无纺布。Next, the fibers were bonded together in the same manner as in Example 1 to obtain a long-fiber nonwoven fabric with a basis weight of 17 g/m 2 .
[实施例5][Example 5]
将单孔喷出量设为0.66g/min·Hole、牵引装置入口的纤维温度设为60℃、牵引空气风速设为5500m/min,与实施例4同样操作,得到平均单纱纤度2.2dtex、单位面积重量20g/m2的长纤维无纺布。The single-hole ejection amount is set to 0.66g/min·Hole, the fiber temperature at the entrance of the traction device is set to 60°C, and the draft air velocity is set to 5500m/min, and the same operation is performed as in Example 4 to obtain an average single yarn fineness of 2.2dtex, Long-fiber non - woven fabric with a unit area weight of 20g/m2.
[实施例6][Example 6]
将牵引装置入口的纤维温度设为50℃、牵引空气风速设为10000m/min,与实施例3同样操作,得到平均单纱纤度2.8dtex、单位面积重量18g/m2的长纤维无纺布。使得到的无纺布在室温22℃的气氛下、在放电量40W·min/m2(放电度4.0W/cm2)的条件下通过电晕放电处理机,得到润湿张力39mN/m的无纺布。The fiber temperature at the entrance of the traction device was set to 50°C, the draft air velocity was set to 10000m/min, and the same operation as in Example 3 was performed to obtain a long-fiber nonwoven fabric with an average single yarn fineness of 2.8dtex and a weight per unit area of 18g/m2. The obtained non-woven fabric was passed through a corona discharge treater under the condition of a discharge capacity of 40 W·min/m 2 (discharge degree 4.0 W/cm 2 ) in an atmosphere at room temperature of 22° C. to obtain a wetting tension of 39 mN/m. non-woven fabric.
通过喷雾法对得到的无纺布施加聚醚系的亲水剂,接着在80℃下热风干燥5分钟,得到亲水剂浓度附着量为0.3重量%的长纤维无纺布。A polyether-based hydrophilic agent was applied to the obtained nonwoven fabric by a spray method, followed by hot air drying at 80° C. for 5 minutes to obtain a long-fiber nonwoven fabric having a hydrophilic agent concentration of 0.3% by weight.
[实施例7][Example 7]
将牵引装置入口的纤维温度设为50℃、牵引空气风速设为12500m/min,与实施例6同样操作,得到平均单纱纤度2.0dtex、单位面积重量15g/m2的、亲水剂浓度附着量为0.5重量%的长纤维无纺布。Set the fiber temperature at the entrance of the traction device to 50°C and the wind speed of the traction air to 12500m/min, and operate in the same manner as in Example 6 to obtain a fiber with an average single yarn fineness of 2.0dtex and a weight per unit area of 15g/m 2 . Long-fiber nonwovens in an amount of 0.5% by weight.
[实施例8][Example 8]
将牵引装置入口的纤维温度设为60℃、牵引空气风速设为5000m/min,与实施例5同样操作,得到平均单纱纤度2.6dtex、单位面积重量17g/m2的长纤维无纺布。使得到的无纺布在室温22℃的气氛下、在放电量40W·min/m2(放电度4.0W/cm2)的条件下通过电晕放电处理机,得到润湿张力39mN/m的无纺布。通过辊舐涂布法对得到的无纺布施加聚醚系的亲水剂,接着在80℃下热风干燥5分钟,得到亲水剂浓度附着量为0.3重量%的长纤维无纺布。The fiber temperature at the entrance of the traction device was set to 60°C, the draft air velocity was set to 5000m/min, and the same operation was performed as in Example 5 to obtain a long-fiber nonwoven fabric with an average single yarn fineness of 2.6dtex and a weight per unit area of 17g/m2. The obtained non-woven fabric was passed through a corona discharge treater under the condition of a discharge capacity of 40 W·min/m 2 (discharge degree 4.0 W/cm 2 ) in an atmosphere at room temperature of 22° C. to obtain a wetting tension of 39 mN/m. non-woven fabric. A polyether-based hydrophilic agent was applied to the obtained nonwoven fabric by the lick roll coating method, followed by hot air drying at 80° C. for 5 minutes to obtain a long-fiber nonwoven fabric having a hydrophilic agent concentration of 0.3% by weight.
[实施例9][Example 9]
混合1.25重量%的熔点为86~90℃(平均熔点88℃)的十八烷酸的甘油酯(氢化动植物油脂),将牵引装置入口的纤维温度设为40℃、牵引空气风速设为17500m/min,与实施例1同样操作,得到平均单纱纤度1.1dtex、单位面积重量17g/m2的长纤维无纺布。Mix 1.25% by weight of stearic acid glyceride (hydrogenated animal and vegetable oil) with a melting point of 86-90°C (average melting point: 88°C), set the fiber temperature at the entrance of the traction device to 40°C, and the traction air velocity to 17500m /min, operate in the same way as in Example 1, obtain the long-fiber nonwoven fabric of average single yarn denier 1.1dtex, weight per unit area 17g/m 2 .
[实施例10][Example 10]
混合3.50重量%的十八烷酸的甘油酯(氢化动植物油脂),将牵引装置入口的纤维温度设为40℃、牵引空气风速设为17500m/min,与实施例1同样操作,制备平均单纱纤度1.1dtex的长纤维纤维网。Mix 3.50% by weight of glycerides of octadecanoic acid (hydrogenated animal and vegetable oils and fats), set the fiber temperature at the entrance of the traction device to 40°C, and set the traction air wind speed to 17500m/min, operate in the same manner as in Example 1, and prepare the average single A long fiber web with a yarn denier of 1.1 dtex.
接着,使得到的纤维网穿过平面辊与压纹辊(图案规格:斜碎点花纹,压接面积率14%)之间,在温度135℃且线性荷载35kgf/cm下将纤维彼此粘接,得到单位面积重量15g/m2的长纤维无纺布。Next, the obtained fiber web was passed between a flat roll and an embossed roll (pattern specification: diagonal broken point pattern, crimping area ratio 14%), and the fibers were bonded to each other at a temperature of 135°C and a linear load of 35kgf/cm , to obtain a long-fiber nonwoven fabric with a weight per unit area of 15 g/m 2 .
[比较例1][Comparative example 1]
将单孔喷出量设为0.22g/min·Hole、牵引装置入口的纤维温度设为40℃、牵引空气风速设为5500m/min,与实施例1同样操作,得到平均单纱纤度1.1dtex、单位面积重量17g/m2的长纤维无纺布。The single-hole ejection amount is set to 0.22g/min·Hole, the fiber temperature at the entrance of the traction device is set to 40°C, and the draft air velocity is set to 5500m/min, and the same operation as in Example 1 is performed to obtain an average single yarn fineness of 1.1dtex, Long - fiber nonwoven fabric with a weight per unit area of 17g/m2.
[比较例2][Comparative example 2]
将单孔喷出量设为0.4g/min·Hole、牵引装置入口的纤维温度设为40℃、牵引空气风速设为4000m/min,与实施例1同样操作,得到平均单纱纤度2.0dtex、单位面积重量20g/m2的长纤维无纺布。The single-hole ejection amount is set to 0.4g/min·Hole, the fiber temperature at the entrance of the traction device is set to 40°C, and the draft air velocity is set to 4000m/min, and the same operation as in Example 1 is performed to obtain an average single yarn fineness of 2.0dtex, Long-fiber non - woven fabric with a unit area weight of 20g/m2.
[比较例3][Comparative example 3]
将牵引装置入口的纤维温度设为40℃、牵引空气风速设为17500m/min,与实施例1同样操作,得到平均单纱纤度1.1dtex的长纤维纤维网。The fiber temperature at the inlet of the drawing device was set at 40° C., the drawing air velocity was set at 17500 m/min, and the operation was the same as in Example 1 to obtain a long-fiber web with an average single yarn fineness of 1.1 dtex.
使得到的纤维网穿过平面辊与压纹辊(图案规格:织眼图案,横间距2.0mm,纵间距2.0mm,压接面积14.4%)之间,将温度设为148℃、线性荷载设为50kgf/cm,得到单位面积重量17g/m2的长纤维无纺布。Make the obtained fiber web pass between the flat roller and the embossing roller (pattern specifications: woven eye pattern, horizontal spacing 2.0mm, vertical spacing 2.0mm, crimping area 14.4%), set the temperature to 148°C, linear load setting It was 50kgf/cm, and a long - fiber nonwoven fabric with a basis weight of 17g/m2 was obtained.
[表1][Table 1]
产业上的可利用性Industrial availability
本发明的无纺布由于热稳定性高、柔软性优异、而且加工性也良好,因此可以适宜地用于卫生材料的顶层片材、底层片材、侧面收集部等。Since the nonwoven fabric of the present invention has high thermal stability, excellent flexibility, and good processability, it can be suitably used for top sheets, back sheets, side collection parts, and the like of hygienic materials.
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