WO2023190074A1 - Tissu non tissé soufflé à l'état fondu et matériau hygiénique - Google Patents
Tissu non tissé soufflé à l'état fondu et matériau hygiénique Download PDFInfo
- Publication number
- WO2023190074A1 WO2023190074A1 PCT/JP2023/011624 JP2023011624W WO2023190074A1 WO 2023190074 A1 WO2023190074 A1 WO 2023190074A1 JP 2023011624 W JP2023011624 W JP 2023011624W WO 2023190074 A1 WO2023190074 A1 WO 2023190074A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- nonwoven fabric
- melt
- molecular weight
- thermoplastic polyurethane
- average molecular
- Prior art date
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 175
- 239000004750 melt-blown nonwoven Substances 0.000 title claims abstract description 171
- 239000000463 material Substances 0.000 title claims description 49
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims abstract description 89
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 89
- 239000000835 fiber Substances 0.000 claims abstract description 84
- 229920001971 elastomer Polymers 0.000 claims abstract description 72
- 239000000806 elastomer Substances 0.000 claims abstract description 72
- 238000009826 distribution Methods 0.000 claims abstract description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 54
- 238000011084 recovery Methods 0.000 claims description 23
- 230000004927 fusion Effects 0.000 claims description 17
- 239000007789 gas Substances 0.000 description 47
- 238000000034 method Methods 0.000 description 38
- 238000009987 spinning Methods 0.000 description 23
- 239000004745 nonwoven fabric Substances 0.000 description 22
- 239000002994 raw material Substances 0.000 description 19
- 239000002028 Biomass Substances 0.000 description 18
- 238000004519 manufacturing process Methods 0.000 description 17
- -1 sanitary masks Substances 0.000 description 17
- 239000011342 resin composition Substances 0.000 description 16
- 239000002245 particle Substances 0.000 description 14
- 238000007711 solidification Methods 0.000 description 13
- 230000008023 solidification Effects 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- 239000000155 melt Substances 0.000 description 9
- 239000002798 polar solvent Substances 0.000 description 9
- 239000012948 isocyanate Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 239000004970 Chain extender Substances 0.000 description 5
- 239000002657 fibrous material Substances 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 229920005862 polyol Polymers 0.000 description 5
- 229920002635 polyurethane Polymers 0.000 description 5
- 239000004814 polyurethane Substances 0.000 description 5
- 229920003225 polyurethane elastomer Polymers 0.000 description 5
- 239000002803 fossil fuel Substances 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 239000005022 packaging material Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 230000002745 absorbent Effects 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000691 measurement method Methods 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 239000012567 medical material Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 240000006394 Sorghum bicolor Species 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 239000012771 household material Substances 0.000 description 2
- 239000012770 industrial material Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920006306 polyurethane fiber Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 229920002725 thermoplastic elastomer Polymers 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- SWSBIGKFUOXRNJ-CVBJKYQLSA-N ethene;(z)-octadec-9-enamide Chemical compound C=C.CCCCCCCC\C=C/CCCCCCCC(N)=O.CCCCCCCC\C=C/CCCCCCCC(N)=O SWSBIGKFUOXRNJ-CVBJKYQLSA-N 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Inorganic materials [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D13/00—Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches
- A41D13/05—Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches protecting only a particular body part
- A41D13/11—Protective face masks, e.g. for surgical use, or for use in foul atmospheres
-
- 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
- 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
- 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
- D04H3/009—Condensation or reaction 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
- D04H3/016—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the fineness
-
- 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
Definitions
- the present disclosure relates to meltblown nonwoven fabrics and sanitary materials.
- nonwoven fabrics have been widely used for various purposes due to their excellent breathability and flexibility. Therefore, nonwoven fabrics are required to have various properties depending on their uses, and improvements in these properties are also required.
- Patent Document 1 discloses a polyurethane fiber nonwoven fabric (hereinafter also simply referred to as "nonwoven fabric").
- the nonwoven fabric disclosed in Patent Document 1 is made of ultrafine polyurethane fibers with an average fiber diameter of 10 ⁇ m or less, and 15 to 80% of the fibers are fused into bundles.
- the nonwoven fabric disclosed in Patent Document 1 has an equilibrium dyeing amount of 60 mg/g or more.
- Patent Document 2 discloses a filter.
- the filter disclosed in Patent Document 2 is made of a fibrous nonwoven fabric whose main component is a thermoplastic elastomer resin.
- the fibrous nonwoven fabric satisfies the following (1) to (4).
- (1) indicates that the average fiber diameter of the fibers constituting the fibrous nonwoven fabric is 10 ⁇ m or less.
- (2) indicates that 15 to 80% of the fibers are composed of two or more fibers fused together in a bundle.
- (3) indicates that the material has an elongation at break of 100% or more and a 50% elongation recovery rate of 60% or more.
- (4) indicates that the air permeability when stretched by 50% in at least one direction is less than twice the air permeability when not stretched.
- Patent Document 3 discloses fibers (hereinafter also simply referred to as "fibers") based on thermoplastic polyurethane.
- the fiber disclosed in Patent Document 3 contains an inorganic additive.
- at least 70% of the particles of the inorganic additive have a maximum particle diameter that is smaller than 75% of the fiber diameter of the thermoplastic polyurethane.
- Patent Document 1 Japanese Patent Application Publication No. 2003-064567
- Patent Document 2 Japanese Patent Application Publication No. 2004-057882
- Patent Document 3 Japanese Patent Publication No. 2010-509512
- nonwoven fabrics can be used for disposable diapers, absorbent materials such as sanitary products, sanitary materials such as sanitary masks, medical materials such as bandages, clothing materials, packaging materials, and the like.
- absorbent materials such as sanitary products
- sanitary materials such as sanitary masks
- medical materials such as bandages, clothing materials, packaging materials, and the like.
- nonwoven fabrics are often required to have excellent elongation at break and water pressure resistance.
- a problem to be solved by an embodiment of the present disclosure is to provide a melt-blown nonwoven fabric with excellent elongation at break and water pressure resistance, and a sanitary material containing the melt-blown nonwoven fabric.
- Means for solving the above problems include the following embodiments.
- ⁇ 1> Heat having a number average molecular weight (Mn) of 100,000 or more and a molecular weight distribution (Mw/Mn), which is the ratio of weight average molecular weight (Mw) to number average molecular weight (Mn), of 2.4 or less.
- Mw/Mn molecular weight distribution
- Mw/Mn molecular weight distribution
- Mw/Mn molecular weight distribution
- ⁇ Meltblown nonwoven fabric larger than g. ⁇ 3> The meltblown nonwoven fabric according to ⁇ 1> or ⁇ 2>, having an average fiber diameter of 5.5 ⁇ m or less.
- ⁇ 4> The meltblown nonwoven fabric according to any one of ⁇ 1> to ⁇ 3>, wherein the thermoplastic polyurethane elastomer satisfies the following formula I.
- a represents the sum of the heat of fusion obtained from endothermic peaks in the range of 90°C to 140°C measured by a differential scanning calorimeter
- b represents 140°C measured by a differential scanning calorimeter.
- Mn number average molecular weight
- ⁇ 6> The meltblown nonwoven fabric according to any one of ⁇ 1> to ⁇ 5>, which has an elongation at break in the MD direction of 250% or more.
- ⁇ 7> The melt-blown nonwoven fabric according to any one of ⁇ 1> to ⁇ 6>, which has a water pressure resistance to basis weight (g/m 2 ) of 6.0 mmH 2 O ⁇ m 2 /g or more.
- ⁇ 8> The meltblown nonwoven fabric according to any one of ⁇ 1> to ⁇ 7>, which has a recovery stress in the MD direction with respect to basis weight (g/m 2 ) of 0.035 N ⁇ m 2 /50 mm ⁇ g or more.
- a sanitary material comprising the meltblown nonwoven fabric according to any one of ⁇ 1> to ⁇ 8>.
- a water-resistant sheet comprising the meltblown nonwoven fabric according to any one of ⁇ 1> to ⁇ 8>.
- a medical sheet comprising the meltblown nonwoven fabric according to any one of ⁇ 1> to ⁇ 8>.
- An embodiment of the present disclosure can provide a meltblown nonwoven fabric with excellent elongation at break and water pressure resistance, and a sanitary material containing the meltblown nonwoven fabric.
- FIG. 1 is a schematic diagram showing an example of the configuration of a meltblown nonwoven fabric manufacturing apparatus 10. As shown in FIG.
- a numerical range expressed using " ⁇ " means a range that includes the numerical values written before and after " ⁇ " as lower and upper limits.
- the amount of each component contained in the composition refers to the total amount of the multiple substances present in the composition. means.
- the upper limit or lower limit described in one numerical range may be replaced with the upper limit or lower limit of another numerical range described step by step. .
- the upper limit or lower limit of the numerical range may be replaced with the values shown in the Examples.
- the amount of each component in the material means the total amount of the multiple substances present in the material, unless otherwise specified.
- the meltblown nonwoven fabric of the present disclosure includes the meltblown nonwoven fabric of the first aspect and the meltblown nonwoven fabric of the second aspect.
- the melt-blown nonwoven fabric of the first aspect and the melt-blown nonwoven fabric of the second aspect will be described below.
- the melt-blown nonwoven fabric of the first aspect has a number average molecular weight (Mn) of 100,000 or more, and a molecular weight distribution (Mw/Mn), which is the ratio of the weight average molecular weight (Mw) to the number average molecular weight (Mn) (hereinafter, It contains a thermoplastic polyurethane elastomer having a molecular weight distribution (Mw/Mn) of 2.4 or less, and has an average fiber diameter of less than 6.5 ⁇ m.
- the melt-blown nonwoven fabric of the first aspect has the above configuration, it has excellent elongation at break and water pressure resistance.
- the thermoplastic polyurethane elastomer in the present disclosure has a relatively large number average molecular weight (Mn). This can increase the breaking strength of the fibers and prevent them from breaking easily. High breaking strength also contributes to improved water pressure resistance.
- the thermoplastic polyurethane elastomer in the present disclosure has a molecular weight distribution (Mw/Mn) of 2.4 or less. This makes the molecular weight in the fiber uniform. This reduces the number of weak portions of molecular chain entanglement that serve as starting points for rupture. As a result, the breaking strength of the fibers and the water pressure resistance of the meltblown nonwoven fabric are improved.
- the average fiber diameter of the melt-blown nonwoven fabric is less than 6.5 ⁇ m, the fiber amount of the melt-blown fibers and, as a result, the self-fusion point increases, and the entanglement becomes strong.
- the combination of the strong intertwining of the fibers and the high breaking strength of the fibers described above produces a synergistic effect in that the entangled fibers can be stretched well without breaking.
- the number average molecular weight (Mn) and weight average molecular weight (Mw) of the thermoplastic polyurethane elastomer refer to the number average molecular weight (Mn) and weight average molecular weight (Mw) in a state included in the meltblown nonwoven fabric.
- the number average molecular weight (Mn) and weight average molecular weight (Mw) of the thermoplastic polyurethane elastomer in a state included in the melt blown nonwoven fabric can vary depending on the conditions when forming the melt blown nonwoven fabric. For example, in Patent Document 1 mentioned above, the molecular weight of the elastomer is considered to be low because the molding temperature is high and the air permeability and elongation at break are extremely low. There is a possibility that high fusion has occurred due to high temperature molding.
- the meltblown nonwoven fabric of the first aspect has an average fiber diameter of less than 6.5 ⁇ m. As a result, the fiber content of the meltblown fibers and, as a result, the self-fusion point increases, and the entanglement becomes stronger.
- the melt-blown nonwoven fabric of the first aspect preferably has an average fiber diameter of 6.4 ⁇ m or less, more preferably 5.5 ⁇ m or less. When the average fiber diameter is 5.5 ⁇ m or less, the fiber amount and self-fusion point of the above-mentioned meltblown fibers further increase, and the entanglement becomes stronger. In addition, thin uneven parts of the nonwoven fabric, which can be the starting point for breakage and water leakage, are reduced. This further improves the elongation at break and the water pressure resistance.
- the melt-blown nonwoven fabric of the first aspect preferably has an average fiber diameter of 2.5 ⁇ m or more, more preferably 3.0 ⁇ m or more.
- the melt-blown nonwoven fabric of the first aspect may have an average fiber diameter of 2.5 ⁇ m or more and less than 6.5 ⁇ m.
- the average fiber diameter is measured by the following method.
- a photograph of the melt-blown nonwoven fabric is taken at a magnification of 1000 times using an electron microscope (eg, Hitachi S-3500N). Measure the diameter of the fiber from the photograph obtained. The imaging and measurement are repeated until the total number of fibers exceeds 100, and the arithmetic mean value of the obtained fiber diameters is defined as the average fiber diameter ( ⁇ m).
- the melt-blown nonwoven fabric of the first embodiment includes a thermoplastic polyurethane elastomer.
- the thermoplastic polyurethane elastomer has a number average molecular weight (Mn) of 100,000 or more. This can increase the breaking strength of the fibers and prevent them from breaking easily. High breaking strength also contributes to improved water pressure resistance.
- the thermoplastic polyurethane elastomer preferably has a number average molecular weight (Mn) of 101,500 or more, more preferably 102,500 or more, and even more preferably 103,500 or more. When the number average molecular weight (Mn) is 101,500 or more, the entanglement of molecular chains further increases, and the breaking strength of the fibers and, by extension, the breaking elongation and water pressure resistance of the nonwoven fabric are further improved.
- the weight average molecular weight (Mw) of the thermoplastic polyurethane elastomer is preferably 180,000 or more, and preferably 190,000 or more.
- the molecular weight distribution (Mw/Mn) of the thermoplastic polyurethane elastomer is 2.4 or less, preferably 2.3 or less, and more preferably 2.2 or less.
- the upper limit of the molecular weight distribution (Mw/Mn) is not particularly limited, but may be, for example, 1.0 or more. In other words, the molecular weight distribution (Mw/Mn) is preferably 1.0 to 2.4, more preferably 1.0 to 2.3, and even more preferably 1.0 to 2.2. preferable.
- the number average molecular weight (Mn), weight average molecular weight (Mw), and molecular weight distribution (Mw/Mn) are measured by the following methods.
- the produced melt-blown nonwoven fabric is heated and melted at 80° C. in the following eluent to produce a measurement sample.
- GPC gel permeation chromatography
- Mn number average molecular weight
- Mw weight average molecular weight
- Mw/Mn molecular weight distribution
- the thermoplastic polyurethane elastomer preferably has a solidification start temperature of 65°C or higher, more preferably 75°C or higher, and even more preferably 85°C or higher.
- solidification start temperature is 65°C or higher, molding defects such as fusion of fibers, thread breakage, and resin lumps can be suppressed when obtaining a meltblown nonwoven fabric, and meltblown molded during hot embossing can be suppressed. It is possible to prevent the nonwoven fabric from wrapping around the embossing roller.
- the thermoplastic solidification start temperature is 65° C. or higher, stickiness of the resulting melt-blown nonwoven fabric can be suppressed. Therefore, melt-blown nonwoven fabrics can be suitably used as materials that come into contact with the skin, such as clothing, sanitary materials, and sports materials.
- the thermoplastic polyurethane elastomer preferably has a solidification start temperature of 195°C or lower. By setting the solidification start temperature to 195° C. or lower, moldability can be improved.
- the solidification onset temperature is measured using a differential scanning calorimeter (DSC). Specifically, the temperature of the thermoplastic polyurethane elastomer is raised to 230°C at a rate of 10°C/min, held at 230°C for 5 minutes, and then lowered at a rate of 10°C/min. The starting temperature of the exothermic peak resulting from the solidification of the thermoplastic polyurethane elastomer that occurs at this time is the solidification start temperature.
- DSC differential scanning calorimeter
- Methods for adjusting the solidification initiation temperature of thermoplastic polyurethane elastomers to 65°C or higher include methods of appropriately selecting the chemical structures of polyol compounds, isocyanate compounds, chain extenders, etc. used as raw materials for thermoplastic polyurethane elastomers; Examples include a method of adjusting the amount of hard segments in the plastic polyurethane elastomer.
- Hard segment amount is the total content of isocyanate compounds and chain extenders used in the production of thermoplastic polyurethane elastomers, divided by the total amount of polyol compounds, isocyanate compounds, and chain extenders, and multiplied by 100. Mass percentage (mass %) value is meant. The amount of hard segments is preferably 20% by mass to 60% by mass, more preferably 22% by mass to 50% by mass, and even more preferably 25% by mass to 48% by mass.
- the thermoplastic polyurethane elastomer preferably has a polar solvent insoluble particle number of preferably 3 million particles (3 million particles/g) or less, more preferably 2.5 million particles per 1 g of the thermoplastic polyurethane elastomer. /g or less, more preferably 2 million pieces/g or less.
- the "polar solvent insoluble matter in the thermoplastic polyurethane elastomer” mainly refers to lumps such as fish eyes and gel that are generated during the production of the thermoplastic polyurethane elastomer.
- Components that cause the generation of polar solvent insoluble matter include components derived from hard segment aggregates of thermoplastic polyurethane elastomers, components in which hard segments and/or soft segments are crosslinked by allophanate bonds, burette bonds, etc. Examples include raw materials constituting the plastic polyurethane elastomer, components generated by chemical reactions between raw materials, and the like.
- the number of particles insoluble in a polar solvent was measured by measuring the insoluble content when a thermoplastic polyurethane elastomer was dissolved in a dimethylacetamide solvent using a particle size distribution measuring device using a pore electrical resistance method equipped with a 100 ⁇ m aperture. It is a value. By installing a 100 ⁇ m aperture, it is possible to measure the number of particles of 2 ⁇ m to 60 ⁇ m in terms of uncrosslinked polystyrene.
- thermoplastic polyurethane elastomer with a small content insoluble in polar solvents can be obtained by carrying out a polymerization reaction of a polyol compound, an isocyanate compound, and a chain extender, followed by filtration.
- the moisture value of the thermoplastic polyurethane elastomer is preferably 350 ppm or less, and 300 ppm or less. It is more preferable that it be present, and even more preferably that it is 150 ppm or less.
- thermoplastic polyurethane elastomer preferably satisfies the following formula I, more preferably satisfies the following formula II, and even more preferably satisfies the following formula III.
- a represents the sum of the heat of fusion obtained from endothermic peaks in the range of 90°C to 140°C measured by differential scanning calorimeter. (Represents the total amount of heat of fusion obtained from endothermic peaks in the range of more than 140 degrees Celsius and less than 220 degrees Celsius measured by
- thermoplastic polyurethane elastomer (heat of fusion ratio)
- a/(a+b) means the heat of fusion ratio (unit: %) of the hard domain of the thermoplastic polyurethane elastomer.
- the heat of fusion ratio of the hard domain of the thermoplastic polyurethane elastomer is 80% or less, the strength and stretchability of the fiber and meltblown nonwoven fabric are improved.
- the lower limit of the heat of fusion ratio of the hard domain of the thermoplastic polyurethane elastomer is preferably about 0.1%.
- the thermoplastic polyurethane elastomer preferably has a melt viscosity (hereinafter also simply referred to as "melt viscosity”) of 100 Pa.s to 3000 Pa.s, and preferably 200 Pa.s to 3000 Pa.s at a temperature of 200° C. and a shear rate of 100 sec -1 It is more preferably 2000 Pa ⁇ s, and even more preferably 900 Pa ⁇ s to 1600 Pa ⁇ s.
- the melt viscosity is measured with a capillograph (manufactured by Toyo Seiki Co., Ltd., with a nozzle length of 30 mm and a diameter of 1 mm).
- thermoplastic polyurethane elastomer having such characteristics can be obtained, for example, by the manufacturing method described in JP-A No. 2004-244791.
- the thermoplastic polyurethane elastomer may contain a biomass raw material. Details of the thermoplastic polyurethane elastomer containing biomass-derived raw materials (biomass-derived thermoplastic polyurethane elastomer) will be described later.
- the melt-blown nonwoven fabric preferably contains 50% by mass or more of a thermoplastic polyurethane elastomer, more preferably 70% by mass or more, even more preferably 90% by mass or more, and particularly preferably 99% by mass or more.
- the basis weight of the melt-blown nonwoven fabric may be determined as appropriate depending on the application.
- the basis weight of the meltblown nonwoven fabric is preferably 1 g/m 2 to 100 g/m 2 , more preferably 4 g/m 2 to 65 g/m 2 .
- the basis weight of meltblown nonwoven fabric is measured by the following method. Six test pieces of 200 mm (machine direction: MD direction) x 50 mm (lateral direction: CD direction) are taken from the melt-blown nonwoven fabric. The sampling locations are any three locations in both the MD and CD directions (six locations in total). Next, the mass (g) of each sampled test piece is measured using an electronic balance (for example, an electronic balance manufactured by Kensei Kogyo Co., Ltd.). Find the average mass of each test piece. The obtained average value is converted into mass (g) per 1 m 2 , and the value rounded to the second decimal place is defined as the basis weight [g/m 2 ] of each sample.
- an electronic balance for example, an electronic balance manufactured by Kensei Kogyo Co., Ltd.
- the thickness of the melt-blown nonwoven fabric may be determined as appropriate depending on the application.
- the thickness of the meltblown nonwoven fabric may be 0.01 mm to 1.00 mm.
- MD (Machine Direction) direction means the flow direction of the fibers.
- the MD (Machine Direction) direction is also the conveyance direction when manufacturing the meltblown nonwoven fabric.
- CD (Cross Direction) direction means a direction perpendicular to the MD direction (that is, the flow direction of the fibers).
- the melt-blown nonwoven fabric of the first aspect preferably has an elongation at break in the MD direction of 250% or more, more preferably 270% or more, even more preferably 300% or more, and even more preferably 340% or more. It is particularly preferable.
- the elongation at break in the MD direction of the melt-blown nonwoven fabric of the first aspect is preferably 700% or less, more preferably 650% or less, and even more preferably 600% or less. It is also preferable that the melt-blown nonwoven fabric of the first aspect has a breaking elongation in the MD direction of 250% or more and 600% or less.
- melt-blown non-woven fabric will resist deformation in the stretching direction in applications where it is necessary to follow the deformation of the human body (for example, disposable diapers, bandages, etc.). It can be tracked well without breaking.
- the melt-blown nonwoven fabric of the first aspect preferably has a breaking elongation in the CD direction of 250% or more, more preferably 350% or more, even more preferably 400% or more, and even more preferably 430% or more. This is particularly preferred.
- the elongation at break in the CD direction of the melt-blown nonwoven fabric of the first aspect is preferably 700% or less, more preferably 650% or less, and even more preferably 600% or less. It is also preferable that the melt-blown nonwoven fabric of the first aspect has a breaking elongation in the CD direction of 250% or more and 600% or less.
- the elongation at break is measured by the following method. Five test pieces of 200 mm (measurement direction) x 50 mm (measurement direction) are taken from the melt-blown nonwoven fabric. The sampling locations are five arbitrary locations. Next, each sampled test piece was stretched in the MD direction of the test piece using a universal tensile tester (for example, model IM-201 manufactured by Intesco) under conditions of a chuck distance of 100 mm and a tensile speed of 100 mm/min. The stretching ratio at which the piece breaks is defined as the elongation at break [%] in the MD direction.
- a universal tensile tester for example, model IM-201 manufactured by Intesco
- the stretching ratio is measured in the same manner as the method for measuring the elongation at break [%] in the MD direction, except that the tensile direction of the test piece is changed from the MD direction of the test piece to the CD direction of the test piece.
- the measured value of the stretching ratio is defined as the elongation at break in the CD direction [%].
- the melt-blown nonwoven fabric of the first aspect preferably has a water pressure resistance (hereinafter also simply referred to as "water pressure resistance") with respect to basis weight (g/m 2 ) of 6.0 mmH 2 O ⁇ m 2 /g or more, and 9.0 mmH It is more preferably 2 O ⁇ m 2 /g or more, and even more preferably 12.0 mmH 2 O ⁇ m 2 /g or more.
- the melt-blown nonwoven fabric of the first aspect preferably has a water pressure resistance of 30.0 mmH 2 O ⁇ m 2 /g or less, more preferably 20.0 mmH 2 O ⁇ m 2 /g or less, and 15.0 mmH 2 More preferably, it is not more than O ⁇ m 2 /g.
- the melt-blown nonwoven fabric of the first aspect has a water pressure resistance of 6.0 mmH 2 O ⁇ m 2 /g or more and 30.0 mmH 2 O ⁇ m 2 /g or less.
- the water pressure resistance is 6.0 mmH 2 O ⁇ m 2 /g or more
- melt-blown nonwoven fabrics are suitable for applications that require liquid leakage resistance (e.g., disposable diapers, sanitary products, etc.). ) can be prevented from leaking.
- the water pressure resistance is a value obtained by dividing the water pressure resistance of the melt-blown nonwoven fabric measured according to method A (low water pressure method) specified in JISL1096 by the basis weight.
- the unit of water pressure resistance of the melt-blown nonwoven fabric is (mmH 2 O)/(g/m 2 ), that is, mmH 2 O ⁇ m 2 /g.
- the melt-blown nonwoven fabric of the first aspect has a recovery stress in the MD direction (hereinafter also simply referred to as "recovery stress in the MD direction”) with respect to basis weight (g/m 2 ) of 0.035 N ⁇ m 2 /50 mm ⁇ g or more. is preferable, and more preferably 0.036 N ⁇ m 2 /50 mm ⁇ g or more.
- the melt-blown nonwoven fabric of the first aspect preferably has a recovery stress in the MD direction of 0.060 N ⁇ m 2 /50 mm ⁇ g or less, more preferably 0.050 N ⁇ m 2 /50 mm ⁇ g or less, and 0.050 N ⁇ m 2 /50 mm ⁇ g or less.
- the melt blown nonwoven fabric of the first aspect has a recovery stress in the MD direction of 0.035 N ⁇ m 2 /50 mm ⁇ g or more and 0.060 N ⁇ m 2 /50 mm ⁇ g or less. If the recovery stress in the MD direction is 0.035 N m 2 /50 mm g or more, the melt blown nonwoven fabric will shrink in applications that need to follow the deformation of the human body (for example, disposable diapers, bandages, etc.). It can follow the deformation in the direction well without remaining stretched.
- the recovery stress in the MD direction is measured by the following method.
- Five test pieces of 200 mm (MD) x 50 mm (CD) are taken from the melt-blown nonwoven fabric.
- the sampling locations are five arbitrary locations.
- each sampled test piece was stretched in the MD direction using a universal tensile tester (for example, IM-201 model manufactured by Intesco) under conditions of a chuck distance of 100 mm, a tensile speed of 100 mm/min, and a stretching ratio of 100%. Afterwards, it is restored to its original length at the same speed.
- a universal tensile tester for example, IM-201 model manufactured by Intesco
- This operation is carried out for two cycles, and the value obtained by dividing the stress when the stretching ratio in the MD direction becomes 50% at the time of recovery in the second cycle by the basis weight is calculated as the MD for the basis weight (g/m 2 ). Let it be the recovery stress in the direction.
- the unit of the recovery stress in the MD direction with respect to the basis weight (g/m 2 ) is (N/50mm)/(g/m 2 ), that is, N ⁇ m 2 /50mm ⁇ g.
- the average fiber diameter of the meltblown nonwoven fabric is preferably 3.0 ⁇ m to 3.7 ⁇ m.
- the thermoplastic polyurethane elastomer preferably has a number average molecular weight (Mn) of 101,500 to 104,000.
- Mn number average molecular weight
- the meltblown nonwoven fabric has an average fiber diameter of 3.0 ⁇ m to 3.7 ⁇ m.
- the average fiber diameter of the meltblown nonwoven fabric is 3.0 ⁇ m to 3.7 ⁇ m, and the basis weight of the meltblown nonwoven fabric is 4 g/m 2 to 30 g/m 2 .
- the thermoplastic polyurethane elastomer has a number average molecular weight (Mn) of 101,500 to 104,000, and the melt blown nonwoven fabric has a basis weight of 4 g/m 2 to 30 g/m 2 .
- the number average molecular weight (Mn) of the thermoplastic polyurethane elastomer is 101,500 to 104,000
- the average fiber diameter of the meltblown nonwoven fabric is 3.0 ⁇ m to 3.7 ⁇ m
- the basis weight of the meltblown nonwoven fabric is It is preferably 4 g/m 2 to 30 g/m 2 .
- melt-blown nonwoven fabric of the first aspect includes, for example, disposable diapers, absorbent articles such as sanitary products, sanitary articles such as sanitary masks, medical articles such as bandages, clothing materials, packaging materials, waterproof sheets, medical sheets, etc. can be mentioned.
- the sanitary material of the present disclosure includes the meltblown nonwoven fabric of the present disclosure.
- the melt-blown nonwoven fabric of the first aspect can be suitably used for top sheets, back sheets, waistbands (e.g. extension tapes, side flaps, etc.), fastening tapes, three-dimensional gathers, and leg cuffs in expandable disposable diapers or pants-type disposable diapers. I can do it.
- the melt-blown nonwoven fabric of the first aspect can be suitably used for parts such as side panels of pants-type disposable diapers. By using the melt-blown nonwoven fabric of the first aspect in these parts, it becomes possible to follow the movements of the wearer and fit the wearer's body, and a comfortable state is maintained even while being worn.
- the melt-blown nonwoven fabric of the first aspect is also suitably used for a disposable mask, etc., which is composed of a mouth-periphery covering part and ear hook parts extending from both sides of the covering part.
- the melt-blown nonwoven fabric of the first aspect is suitably used as a base material for movable joints such as arms, elbows, and shoulders in disposable surgical gowns, rescue gowns, and the like.
- the water-resistant sheet of the present disclosure preferably includes the melt-blown nonwoven fabric of the present disclosure.
- the water-resistant sheet of the present disclosure may have any known configuration except that it includes the melt-blown nonwoven fabric of the present disclosure.
- the water-resistant sheet of the present disclosure may be made of the melt-blown non-woven fabric of the present disclosure, or may include a layer made of the melt-blown non-woven fabric of the present disclosure (hereinafter also referred to as "melt-blown non-woven fabric layer") and known fibers (for example, cellulose fibers). etc.) (hereinafter also referred to as a "fibrous layer").
- the fibrous layer is laminated on one main surface of the meltblown nonwoven fabric layer.
- the water-resistant sheet of the present disclosure can be used for absorbent materials such as disposable diapers and sanitary products, sanitary materials such as sanitary masks and cosmetic materials, medical materials such as bandages, household materials such as clothing materials and packaging materials, and industrial materials such as filters. It can be used for purposes such as In particular, it has excellent flexibility, breathability, stretchability, and barrier properties, so it is suitably used for sanitary materials such as paper diapers, sanitary napkins, base fabrics for poultice materials, and bed covers. Examples of medical materials and clothing materials include gowns, caps, drapes, masks, gauze, bandages, and various protective clothing.
- it has good post-processing properties such as heat sealing, so it can be used to wrap oxygen absorbers, body warmers, hot air bags, masks, various powders, semi-solids, gels, and liquid substances, CD (compact disc) bags, and food products. It can be applied to all kinds of household materials such as packaging materials, clothing covers, and agricultural sheets. For the same reason, it can also be suitably used as an industrial material such as automobile interior materials, various backing materials, and building materials. Furthermore, since it is composed of fine fibers, it can be widely applied as a material for liquid filters and air filters.
- the medical sheet of the present disclosure includes the melt-blown nonwoven fabric of the present disclosure.
- the medical sheet of the present disclosure may have any known configuration except that it includes the melt-blown nonwoven fabric of the present disclosure.
- the medical sheet of the present disclosure may be made of a meltblown nonwoven fabric, or may include a meltblown nonwoven fabric layer and a fiber layer.
- the fibrous layer is laminated on one main surface of the meltblown nonwoven fabric layer.
- the medical sheet of the present disclosure is suitably used for materials such as gowns, caps, drapes, masks, gauze, bandages, and various protective clothing, plaster base fabrics, poultice materials, wound dressings, wound tapes, and the like.
- raw materials that are stable against electron beams and gamma rays that are irradiated during sterilization and sterilization they can be suitably used for sterilized medical sheets.
- Biomass-derived thermoplastic polyurethane elastomers can also be obtained by polymerizing propylene obtained by dehydrating isopropanol produced by fermentation from biomass raw materials mainly made of inedible plants such as sorghum.
- biomass degree indicates the content rate of carbon derived from biomass, and is calculated by measuring radioactive carbon (C14). Since carbon dioxide in the atmosphere contains C14 at a certain rate (approximately 105.5 pMC), the C14 content in plants (e.g. corn) that grow by taking in atmospheric carbon dioxide is also approximately 105.5 pMC. It is known that the degree of It is also known that fossil fuels contain almost no C14. Therefore, by measuring the proportion of C14 contained in all carbon atoms in the raw material, the content rate of biomass-derived carbon in the raw material can be calculated.
- C14 radioactive carbon
- the content rate Pbio (%) of biomass-derived carbon in the raw material can be calculated using the following formula (1).
- Pbio (%) PC14/105.5 ⁇ 100...Formula (1)
- biomass-derived carbon is theoretically 100%, so the biomass degree of the biomass-derived thermoplastic polyurethane elastomer is 100%.
- biomass-derived raw materials hardly contain C14, the content of biomass-derived carbon in polyurethane produced only from fossil fuel-derived raw materials is 0%, and the biomass content of fossil fuel-derived polyurethane is 0%. becomes 0%.
- the biomass content of the biomass-derived polyurethane thermoplastic elastomer used as a raw material for the spunbond nonwoven fabric of the present disclosure is preferably 1% or more.
- thermoplastic polyurethane elastomers are manufactured using polymer glycols such as polyether polyols, polyester polyols, and polycarbonate polyols; short chain glycols (chain extenders) such as aliphatic glycols, aromatic glycols, and alicyclic glycols as raw materials. and isocyanate compounds such as aromatic diisocyanates, aliphatic diisocyanates, and alicyclic diisocyanates.
- the isocyanates preferably used include aliphatic isocyanates such as 1,5-pentamethylene diisocyanate-based polyisocyanate (trade name: Stabio (registered trademark)) manufactured by Mitsui Chemicals, Inc., aromatic isocyanates, etc. Can be mentioned.
- the thermoplastic polyurethane elastomer used as the raw material for the spunbond nonwoven fabric of the present disclosure may contain a so-called recycled polymer obtained by recycling.
- Recycled polymer includes a polymer obtained by recycling waste polymer products, and can be produced, for example, by the method described in DE102019127827 (A1).
- the recycled polymer may include a marker that allows it to be identified as having been obtained through recycling.
- the melt-blown nonwoven fabric of the second aspect has a number average molecular weight (Mn) of 100,000 or more, and a molecular weight distribution (Mw/Mn), which is the ratio of the weight average molecular weight (Mw) to the number average molecular weight (Mn) (hereinafter, It contains a thermoplastic polyurethane elastomer with a recovery stress in the MD direction (hereinafter simply referred to as “recovery in the MD direction”) with respect to basis weight (g/m 2 ) of 2.4 or less (also simply referred to as "molecular weight distribution (Mw/Mn)"). (also referred to as "stress”) is greater than 0.034N ⁇ m 2 /50mm ⁇ g.
- the melt-blown nonwoven fabric of the second aspect has excellent elongation at break and water pressure resistance.
- the thermoplastic polyurethane elastomer in the present disclosure has a relatively large number average molecular weight (Mn). This can increase the breaking strength of the fibers and prevent them from breaking easily. High breaking strength also contributes to improved water pressure resistance.
- the thermoplastic polyurethane elastomer in the present disclosure has a molecular weight distribution (Mw/Mn) of 2.4 or less. This makes the molecular weight in the fiber uniform. This reduces the number of weak portions of molecular chain entanglement that serve as starting points for rupture. As a result, the breaking strength of the fibers and the water pressure resistance of the nonwoven fabric are improved.
- the fact that the recovery stress in the MD direction is greater than 0.034 N ⁇ m 2 /50 mm ⁇ g indicates that the structure of the hard segment and soft segment of the thermoplastic polyurethane elastomer is sufficiently formed. This can suppress plastic deformation of the fibers. As a result, even when high water pressure is applied, the fibers can maintain their shape, the opening of the fibers is suppressed, and the water pressure resistance is improved.
- the hard segments of the thermoplastic polyurethane elastomer are sufficiently formed, the entanglement of the polyurethane molecules in the fibers is easily maintained, and the fibers can be elastically deformed to a high elongation without breaking.
- the combination of the high elongation of the fibers and the high breaking strength of the fibers described above provides a synergistic effect in that the entangled fibers can be stretched well without breaking.
- each item described in the section of the first aspect can also be applied to the second aspect.
- the details of the preferred range, definition, measuring method, etc. of the average fiber diameter in the second aspect are the same as the details of the preferred range, definition, measuring method, etc. of the average fiber diameter in the first aspect.
- melt viscosity Details of the number average molecular weight (Mn) of the thermoplastic polyurethane elastomer in the first embodiment, Weight average molecular weight (Mw), molecular weight distribution (Mw/Mn), solidification start temperature, hard segment amount, number of particles insoluble in polar solvent, moisture value, formula I, formula II, formula III, heat of fusion ratio, melt viscosity,
- Mw Weight average molecular weight
- Mw/Mn molecular weight distribution
- solidification start temperature Details of the number average molecular weight (Mw), molecular weight distribution (Mw/Mn), solidification start temperature, hard segment amount, number of particles insoluble in polar solvent, moisture value, formula I, formula II, formula III, heat of fusion ratio, melt viscosity,
- the details are the same as the preferred range of content, definition, measurement method, etc.
- the details of the preferred ranges, preferred embodiments, definitions, measurement methods, etc. of the melt-blown nonwoven fabric in the second aspect include the
- the method for producing a melt-blown nonwoven fabric of the present disclosure includes a step (hereinafter, “ (also referred to as “fiberization process”).
- a melt of the resin composition is discharged from a spinneret together with a heated gas, and the discharged melt of the resin composition (hereinafter also referred to as “discharged product”) is stretched by the heated gas.
- the method for producing a meltblown nonwoven fabric of the present disclosure is a method for producing a meltblown nonwoven fabric by a meltblown method using a resin composition.
- a method for producing a melt-blown nonwoven fabric using a thermoplastic polyurethane elastomer by a melt-blown method is described in, for example, JP-A-2003-64567 (Patent Document 1), JP-A-2004-57882, and the like.
- the "melt blown method” is a process in which a molten resin composition is discharged from a spinneret in the form of fibers, and heated gas is applied to the discharged material from both sides of the fiber-shaped discharged material, and heated gas is applied to the moving discharged material.
- This is a method of reducing the diameter of the ejected material by making it accompany the ejected material.
- a resin composition as a raw material is melted using an extruder or the like.
- the molten resin composition is introduced into a spinneret connected to the tip of the extruder, and is discharged in the form of fibers from the spinning nozzle of the spinneret.
- a heated gas ejected from a gas nozzle of a spinneret is applied to the fibrous material, and the heated gas stretches the fibrous material, thereby making the fibrous material thinner.
- the resin composition only needs to contain the thermoplastic polyurethane elastomer according to the present disclosure, and may be the thermoplastic polyurethane elastomer itself according to the present disclosure, or the thermoplastic polyurethane elastomer according to the present disclosure and other resins. and at least one of an additive.
- the temperature (Ta) of the heating gas may be appropriately selected depending on the type of thermoplastic polyurethane elastomer.
- the temperature (Ta) of the heating gas may be, for example, 210°C to 240°C.
- the temperature (Tp) of the melt of the resin composition may be appropriately selected depending on the type of thermoplastic polyurethane elastomer.
- the temperature (Tp) of the melt of the resin composition may be, for example, 200°C to 230°C.
- the temperature (Tp) of the melt of the resin composition can be measured as the set temperature of the spinneret (die).
- the temperature (Ta) of the heated gas can be measured as the temperature of the heated gas immediately after being discharged from the spinneret (die). Specifically, the temperature of the heated gas (Ta) can be measured as the temperature of the heated gas at the opening of the gas nozzle of the spinneret (die).
- the temperature (Ta) of the heated gas can be adjusted, for example, while measuring the temperature (Ta) of the heated gas at the opening of the gas nozzle of the spinneret (die), until the temperature (Ta) of the heated gas at the opening of the gas nozzle is set to a predetermined value.
- the temperature of the heated gas at the opening of the gas nozzle (Ta) may be adjusted under predetermined conditions (e.g., die temperature, heated gas flow rate).
- Data showing the relationship between the temperature and the supply temperature of the heated gas is prepared in advance, and based on that data, the temperature of the heated gas (Ta) at the opening of the gas nozzle is set to a predetermined temperature. This may also be done by adjusting the supply temperature of the heating gas.
- the discharge amount of the melt of the resin composition per spinning nozzle of the spinneret may be, for example, 0.05 g/min to 0.20 g/min.
- the flow rate of the heating gas may be between 300 Nm 3 /hr/m and 500 Nm 3 /hr/m.
- the type of heating gas is not particularly limited, and examples include gases that are inert to the melted resin composition (eg, air, carbon dioxide gas, nitrogen gas, etc.). Among these, air is preferred from the viewpoint of economy.
- the method for producing a meltblown nonwoven fabric of the present disclosure may further include a step of collecting the fibrous extrudate in the form of a web after performing the above-described fiberizing step.
- the obtained discharged material is collected in the form of a web on a collector, for example.
- the ejected material is collected by suctioning air from the side of the collector opposite to the surface that collects the ejected material (hereinafter also referred to as the "back side"). May be promoted.
- collectors include perforated belts, perforated drums, and the like. Note that collection of fibrous materials may be promoted by sucking air from the back side of the collector. The ejected material may be collected on a desired base material provided in advance on the collector. Examples of pre-provided substrates include other nonwoven fabrics (eg, meltblown nonwoven fabrics, spunbond nonwoven fabrics, needle punched and spunlaced nonwoven fabrics, etc.), woven fabrics, knitted fabrics, paper, and the like.
- nonwoven fabrics eg, meltblown nonwoven fabrics, spunbond nonwoven fabrics, needle punched and spunlaced nonwoven fabrics, etc.
- meltblown nonwoven fabric manufacturing apparatus used in the meltblown nonwoven fabric manufacturing method of the present disclosure will be described with reference to FIG. 1.
- FIG. 1 is a schematic diagram showing an example of the configuration of a meltblown nonwoven fabric manufacturing apparatus 10.
- a meltblown nonwoven fabric manufacturing apparatus 10 includes an extruder 20, a die (spinneret) 30, and a collection mechanism 40.
- the extruder 20 has a hopper 21 and a compression section 22.
- the extruder 20 melts the solid material of the resin composition introduced into the hopper 21 in the compression section 22 .
- the extruder 20 may be a single-screw extruder or a multi-screw extruder such as a twin-screw extruder.
- a die (spinneret) 30 is connected to the tip of the extruder 20 and arranged.
- the die 30 has a plurality of spinning nozzles 31 and two gas nozzles 32.
- the plurality of spinning nozzles 31 are usually arranged in a row.
- the spinning nozzle 31 discharges the melted resin composition melted by the compression section 22 in the form of fibers from the nozzle opening.
- the diameter of the spinning nozzle can be, for example, between 0.08 mm and 0.60 mm.
- the temperature (Tp) of the melt of the resin composition can be adjusted by the set temperature of the die 30.
- the distance between the small holes in the spinning nozzle of the spinneret may be 0.5 mm to 3.0 mm.
- the two gas nozzles (air nozzles) 32 are arranged near the nozzle opening of the spinning nozzle 31 (specifically, on both sides of the row of the plurality of spinning nozzles 31).
- the gas nozzle 32 injects heated gas (heated compressed gas) near the opening of the spinning nozzle 31 . As shown in FIG. 1, the gas nozzle 32 injects heated gas to the discharged material immediately after being discharged from the opening of the spinning nozzle 31.
- the heating gas supplied to the gas nozzle 32 is supplied from the gas heating device 50.
- the temperature (Ta) of the heating gas can be adjusted by a heating temperature adjustment means (not shown) attached to the gas heating device 50.
- the collection mechanism 40 includes a perforated belt (collector) 41, a roller 42 that supports and transports the belt, and an air suction unit 43 arranged on the back side of the collection surface of the perforated belt 41.
- the air suction section 43 is connected to a blower 44.
- the collection mechanism 40 collects the fibrous discharge material onto a moving porous belt 41 .
- the molten resin composition melted in the extruder 20 is introduced into the spinning nozzle 31 of the die (spinneret) 30 and discharged from the opening of the spinning nozzle 31. Heated gas is injected from the gas nozzle 32 toward the vicinity of the opening of the spinning nozzle 31 .
- the fibrous material discharged from the spinning nozzle 31 is stretched and thinned by the heated gas.
- the temperature (Ta) of the heating gas is adjusted appropriately. Thereby, the discharged material is appropriately rapidly cooled and stretched.
- the flow rate of the heating gas is adjusted to satisfy the above range. Thereby, even if the discharged material is rapidly cooled, it can be sufficiently stretched. Then, the discharged material is collected on the porous belt 41 to obtain a meltblown nonwoven fabric.
- the above-described melt-blown nonwoven fabric of the present disclosure and the melt-blown nonwoven fabric produced by the above-described manufacturing method may be electrically charged.
- the charging method is not particularly limited as long as the melt-blown non-woven fabric can be made into an electret; for example, a corona charging method, a method of applying water or an aqueous solution of a water-soluble organic solvent to the melt-blown non-woven fabric and then drying it to make it an electret (for example, methods described in Japanese Patent Publication No. Hei 9-501604, Japanese Patent Application Laid-open No. 2002-115177, etc.) can be mentioned.
- the electric field strength is preferably 15 kV/cm or more, more preferably 20 kV/cm or more.
- the permissible range of elongation at break in the MD direction is 300% or more.
- the permissible range of elongation at break in the CD direction is 300% or more.
- Mn number average molecular weight
- thermoplastic polyurethane elastomer [TPU (1)].
- the obtained TPU (1) had Shore A hardness: 82, melting point (Tm) (high melting point side): 162.2°C, heat of fusion: 11.4 mJ/mg, melt viscosity: 1100 Pa ⁇ s, solidification start temperature 155 °C, heat of fusion of hard domain: 0.58.
- Example 1 A meltblown nonwoven fabric was produced as follows. TPU (1) was melted using a single screw extruder. The molten TPU (1) was supplied to the die, and from the die with a set temperature of 220°C (temperature of the molten TPU (1)), the amount of discharge per spinning nozzle was 0.067 g/min. It was discharged together with heated air (temperature Ta: 230°C, flow rate: 5.4 Nm 3 /cm/hour) blown from both sides. The diameter of the spinning nozzle of the die was 0.38 mm. Then, the fibrous extrudate was collected on a collector so that the basis weight became the value shown in Table 1, to obtain a meltblown nonwoven fabric. Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 2 The procedure was the same as in Example 1, except that the flow rate of the heated air was changed from 5.4 Nm 3 /cm / hour to 6.8 Nm 3 /cm / hour, and the basis weight was changed to the value listed in Table 1.
- a meltblown nonwoven fabric was obtained.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 3 The discharge amount per spinning nozzle was changed from 0.067 g/min to 0.106 g/min, the flow rate of heated air was changed from 5.4 Nm 3 /cm/hour to 6.8 Nm 3 /cm/hour, A meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the basis weight was changed to the value shown in Table 1.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 4 The discharge amount per spinning nozzle was changed from 0.067 g/min to 0.142 g/min, the flow rate of heated air was changed from 5.4 Nm 3 /cm/hour to 6.8 Nm 3 /cm/hour, A meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the basis weight was changed to the value shown in Table 1.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 5 A meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the moving speed of the collector was changed so that the basis weight was changed to the value shown in Table 1.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 6 A meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the moving speed of the collector was changed so that the basis weight was changed to the value shown in Table 1.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 7 The set temperature of the die was changed from 220°C to 215°C, the discharge amount per spinning nozzle was changed from 0.067g/min to 0.047g/min, and the flow rate of heated air was changed to 5.4Nm 3 /cm/hour.
- a meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the weight was changed from 4.1 Nm 3 /cm/hour to 4.1 Nm 3 /cm/hour, and the basis weight was changed to the value shown in Table 1.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 8 The set temperature of the die was changed from 220°C to 215°C, the discharge amount per spinning nozzle was changed from 0.067g/min to 0.047g/min, and the flow rate of heated air was changed to 5.4Nm 3 /cm/hour.
- a meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the weight was changed from 4.1 Nm 3 /cm/hour to 4.1 Nm 3 /cm/hour, and the basis weight was changed to the value shown in Table 1.
- Table 1 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 1 A meltblown nonwoven fabric was obtained in the same manner as in Example 4, except that the moving speed of the collector was changed so that the basis weight was changed to the value shown in Table 2.
- Table 2 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- Example 3 The set temperature of the die was changed from 220°C to 230°C, the discharge amount per spinning nozzle was changed from 0.067g/min to 0.106g/min, and the flow rate of heated air was changed to 5.4Nm 3 /cm/hour.
- a meltblown nonwoven fabric was obtained in the same manner as in Example 1, except that the weight was changed from 6.7 Nm 3 /cm/hour to 6.7 Nm 3 /cm/hour, and the basis weight was changed to the value shown in Table 2.
- Table 2 shows the average fiber diameter of the melt-blown nonwoven fabric, the molecular weight of TPU (1) contained in the melt-blown nonwoven fabric, the elongation at break in the MD and CD directions, and the water pressure resistance.
- melt-blown nonwoven fabrics of Examples 1 to 8 have a number average molecular weight (Mn) of 100,000 or more and a molecular weight distribution (Mw/Mn) of 2.4 or less.
- Mn number average molecular weight
- Mw/Mn molecular weight distribution
- the melt-blown nonwoven fabrics of Examples 1 to 8 contain a thermoplastic polyurethane elastomer having a number average molecular weight (Mn) of 100,000 or more and a molecular weight distribution (Mw/Mn) of 2.4 or less, and have a basis weight ( g/m 2 ) is greater than 0.034 N ⁇ m 2 /50 mm ⁇ g.
- the elongation at break in the MD direction and the elongation at break in the CD direction are each 300% or more, and the water pressure resistance is 4.0 (mmH 2 O)/(g/m 2 ).
- the elongation at break and water pressure resistance of Examples 1 to 8 were excellent.
- the melt-blown nonwoven fabric of Comparative Example 1 had an average fiber diameter not less than 6.5 ⁇ m and a recovery stress in the MD direction relative to the basis weight (g/m 2 ) of not more than 0.034 N ⁇ m 2 /50 mm ⁇ g.
- the water pressure resistance of the meltblown nonwoven fabric of Comparative Example 1 was less than 4.0 (mmH 2 O)/(g/m 2 ), which was inferior to Examples 1 to 8.
- the melt-blown nonwoven fabrics of Comparative Examples 2 and 3 did not use a thermoplastic polyurethane elastomer having a number average molecular weight (Mn) of 100,000 or more. Therefore, each of the MD breaking elongation and CD breaking elongation of Comparative Examples 2 and 3 was less than 300%, which was inferior to Examples 1 to 8.
- the meltblown nonwoven fabric broke at the stage of stretching at a stretching ratio of 100%. Therefore, the recovery stress of Comparative Example 2 could not be measured.
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- General Health & Medical Sciences (AREA)
- Vascular Medicine (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nonwoven Fabrics (AREA)
- Absorbent Articles And Supports Therefor (AREA)
Abstract
Le tissu non tissé soufflé à l'état fondu selon la présente invention comprend un élastomère à base de polyuréthane thermoplastique ayant un poids moléculaire moyen en nombre (Mn) supérieur ou égal à 100 000 et une distribution moléculaire (Mw/Mn), qui est un rapport du poids moléculaire moyen en poids (Mw) à un poids moléculaire moyen en nombre (Mn), inférieur ou égal à 2,4 et a un diamètre de fibre moyen inférieur à 6,5 µm.
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CN117552183A (zh) * | 2023-10-31 | 2024-02-13 | 黄河三角洲京博化工研究院有限公司 | 一种弹性非织造布及其制作工艺和应用 |
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WO1993001222A1 (fr) * | 1991-07-03 | 1993-01-21 | Kanebo, Ltd. | Elastomere de polyurethane thermoplastique, procede et dispositif de production, et fibre elastique realisee a partir de cet elastomere |
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WO2016143833A1 (fr) * | 2015-03-09 | 2016-09-15 | 三井化学株式会社 | Stratifié de tissu non tissé, stratifié de tissu non tissé étirable, produit de fibre, article absorbant et masque hygiénique |
JP2017056565A (ja) * | 2015-09-14 | 2017-03-23 | 日立化成株式会社 | 複合体及びその製造方法 |
WO2020218092A1 (fr) * | 2019-04-26 | 2020-10-29 | クラレクラフレックス株式会社 | Corps stratifié de fibres et son procédé de production |
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- 2023-03-23 WO PCT/JP2023/011624 patent/WO2023190074A1/fr unknown
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JPH0411061A (ja) * | 1990-04-27 | 1992-01-16 | Asahi Chem Ind Co Ltd | 伸縮性不織布とその製造法 |
WO1993001222A1 (fr) * | 1991-07-03 | 1993-01-21 | Kanebo, Ltd. | Elastomere de polyurethane thermoplastique, procede et dispositif de production, et fibre elastique realisee a partir de cet elastomere |
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WO2016143833A1 (fr) * | 2015-03-09 | 2016-09-15 | 三井化学株式会社 | Stratifié de tissu non tissé, stratifié de tissu non tissé étirable, produit de fibre, article absorbant et masque hygiénique |
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CN117552183A (zh) * | 2023-10-31 | 2024-02-13 | 黄河三角洲京博化工研究院有限公司 | 一种弹性非织造布及其制作工艺和应用 |
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