WO2014050965A1 - スパンボンド不織布 - Google Patents
スパンボンド不織布 Download PDFInfo
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- WO2014050965A1 WO2014050965A1 PCT/JP2013/076061 JP2013076061W WO2014050965A1 WO 2014050965 A1 WO2014050965 A1 WO 2014050965A1 JP 2013076061 W JP2013076061 W JP 2013076061W WO 2014050965 A1 WO2014050965 A1 WO 2014050965A1
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- WIPO (PCT)
- Prior art keywords
- nonwoven fabric
- propylene
- melting point
- propylene polymer
- weight
- Prior art date
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Classifications
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- 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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/26—Synthetic macromolecular compounds
- B01J20/261—Synthetic macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
- D01F6/06—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins from polypropylene
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/46—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
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- 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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
- Y10T442/642—Strand or fiber material is a blend of polymeric material and a filler material
Definitions
- the present invention relates to a spunbonded nonwoven fabric including polypropylene, which has excellent flexibility, bending resistance, touch and strength. Specifically, the present invention relates to a polypropylene-based spunbonded nonwoven fabric that can be suitably used as a material for absorbent articles such as disposable diapers.
- nonwoven fabrics are widely used for various applications because of their excellent breathability and flexibility. For this reason, the nonwoven fabric is required to have various properties according to its use and to improve the properties.
- disposable diapers that require absorption properties to quickly transfer discharged or excreted menstrual blood, urine, and other liquids to the absorber, and surface properties that are soft to touch the wearer's skin and have little irritation to the skin It is widely used as a surface sheet for absorbent articles such as sanitary napkins.
- water resistance that prevents the liquid absorbed by the internal absorber from leaking to the outside and moisture permeation for preventing moisture due to moisture generated inside and allowing moisture inside the absorbent article to permeate and dissipate to the outside It is also widely used as a backside sheet that is required. Further, since this back sheet constitutes the surface of the absorbent article, it is required to have excellent texture and good tactile sensation.
- Thermoplastic long fiber nonwoven fabrics such as spunbonded nonwoven fabrics are used in many fields because they are excellent in continuous spinning and productivity, as well as mechanical properties such as tensile strength, bending resistance, and breathability. It is coming.
- thermoplastic resins used in these long-fiber nonwoven fabrics polyamide resins, polyester resins, and polyolefin resins are used from the viewpoint of melt spinnability and fiber characteristics. Especially in absorbent articles, they are inexpensive and workable. In order to improve the touch, resin compositions obtained by adding other resins and lubricants to the polyolefin resin are often used.
- Patent Document 1 discloses a spunbonded nonwoven fabric made of a polyolefin resin, particularly a polypropylene resin, having a static friction coefficient in the range of 0.1 to 0.4.
- Patent Document 1 discloses that a nonwoven fabric contains a fatty acid amide compound as a lubricant.
- Patent Document 2 also discloses a polyolefin nonwoven fabric containing a fatty acid amide compound, particularly erucic acid amide, as a lubricant.
- Patent Document 7 International Publication No. WO2012 / 07518 (Patent Document 7) as a spunbond nonwoven fabric using a resin composition in which low crystalline polypropylene is selected as another resin among the above resin compositions. is doing.
- Patent Documents 3, 4, 5, and 6 use a resin composition in which an ⁇ -olefin copolymer or a low crystalline polypropylene is added to a propylene-based polymer for the purpose of improving flexibility.
- an ⁇ -olefin copolymer or a low crystalline polypropylene is added to a propylene-based polymer for the purpose of improving flexibility.
- the added ⁇ -olefin copolymer or low crystalline polypropylene is deposited on the surface of the fiber forming the spunbonded nonwoven fabric, and the touch of the nonwoven fabric is impaired.
- these documents have descriptions relating to the addition of lubricants, but do not suggest specific descriptions of lubricants or their specific effects.
- the object of the present invention is to provide a spunbonded nonwoven fabric containing polypropylene and having excellent balance of flexibility, touch and strength.
- a spunbonded nonwoven fabric comprising a propylene-based polymer composition comprising a propylene-based polymer (A) having a melting point of 120 ° C. or higher and a fatty acid amide having 15 to 21 carbon atoms.
- a spunbond nonwoven fabric according to [1] wherein the fatty acid amide having 15 to 21 carbon atoms is oleic acid amide.
- the propylene-based polymer composition has a melting point of 120 ° C. or more and a total of 100 parts by weight of the propylene-based polymer (A) having a melting point of less than 120 ° C.
- the propylene polymer (B) having a melting point of less than 120 ° C. is a propylene homopolymer or a random copolymer composed of propylene and an ⁇ -olefin having 4 to 20 carbon atoms.
- Spunbond nonwoven fabric is a propylene homopolymer or a random copolymer composed of propylene and an ⁇ -olefin having 4 to 20 carbon atoms.
- a nonwoven fabric laminate comprising the spunbonded nonwoven fabric of [1] to [10].
- the spunbonded nonwoven fabric of the present invention contains a fatty acid amide having a carbon number of 15 to 21 together with a propylene polymer (A) having a melting point of 120 ° C. or higher, so that both softness and fluffy feeling and smooth feeling can be achieved.
- a propylene polymer (A) having a melting point of 120 ° C. or higher so that both softness and fluffy feeling and smooth feeling can be achieved.
- the propylene polymer (B) having a melting point of less than 120 ° C. is contained, the resulting nonwoven fabric has high flexibility, bending resistance and tactile sensation.
- the spunbonded nonwoven fabric of the present invention is suitable for uses such as sanitary products and disposable diapers because it has such flexibility, is less likely to fluff, and is excellent in strength and workability.
- the propylene-based polymer (A) forming the spunbonded nonwoven fabric of the present invention has a melting point measured by a differential scanning calorimeter of 120 ° C. or higher, preferably 120 to 170 ° C.
- the propylene-based polymer (A) according to the present invention has crystallinity and has an isotactic index I.D. I. It is desirable to use polypropylene having a (boiling n-heptane insoluble component) of preferably 75% by weight or more, more preferably 75 to 99% by weight.
- the melt flow rate (ASTMAD1238, temperature 230 ° C., load 2160 g) of the propylene polymer (A) is 1 to 300 g / 10 minutes, preferably 2 to 200 g / 10 minutes. When the melt flow rate is within this range, melt spinning can be performed.
- the propylene polymer (A) may be either a propylene homopolymer or a random copolymer composed of propylene and an ⁇ -olefin, or a propylene homopolymer, a random composed of propylene and an ⁇ -olefin. A combination with a copolymer may also be used. From the viewpoint of strength in the resulting nonwoven fabric, a propylene homopolymer is preferred. Further, when a random copolymer composed of propylene and ⁇ -olefin is used in combination with a propylene homopolymer, it is possible to improve the tactile sensation. In this case, the random copolymer is 100 weights in total with the propylene homopolymer. % In the range of 0.1 to 30% by weight.
- block polypropylene may be used as the polymer (A).
- a conventionally well-known thing can be used as such a propylene polymer (A), and it can obtain easily from a market.
- examples of the propylene homopolymer include “Prime Polypropylene S119” (trade name; manufactured by Prime Polymer Co., Ltd.).
- examples of the copolymer of propylene and ethylene include ExxonMobil's product name: Vistamaxx VM2125.
- the propylene polymer (A) can be produced by a known method using a conventionally known solid titanium catalyst (Ziegler catalyst) component or metallocene compound catalyst component.
- the propylene polymer (A) may be used alone, but when the propylene polymer (B) shown below is used together with the propylene polymer (A), Since flexibility, bending resistance, and touch are particularly excellent, it is preferable.
- the propylene-based polymer (B) used in the present invention is a propylene-based polymer having a melting point of less than 120 ° C. Even if it is a propylene homopolymer, the propylene and the ⁇ -carbon having 2 or 4 to 20 carbon atoms are used. It may be a copolymer with olefin. Among these, in the present invention, a propylene homopolymer or a copolymer of propylene and an ⁇ -olefin having 4 to 20 carbon atoms is preferable.
- the melting point (Tm) measured with a differential scanning calorimeter is less than 120 ° C., preferably 110 ° C. or less, more preferably 50 to 100 ° C., further preferably 55 to 85 ° C., most preferably 60 to 80 ° C. .
- the melt flow rate (ASTM D1238, temperature 230 ° C., load 2160 g) of the propylene polymer (B) is 1 to 1000 g / 10 minutes, preferably 2 to 500 g / 10 minutes, more preferably 2 to 250 g / 10. Min, most preferably 2 to 150 g / 10 min.
- the melt flow rate is within this range, the nonwoven fabric obtained when combined with the propylene-based polymer (A) is excellent in flexibility, bending resistance and touch.
- ⁇ -olefin when a copolymer of propylene and an ⁇ -olefin having 4 to 20 carbon atoms is used as the propylene polymer (B) include 1-butene, 1-pentene, Examples include 1-hexene, 1-heptene, 1-octene, 1-decene, 1-dodecene, 1-hexadecene, and 4-methyl-1-pentene. Of these, 1-butene is preferred.
- the ⁇ -olefin content in the copolymer is not particularly limited as long as the melting point (Tm) of the resulting propylene polymer is in the above range, but is usually 0.1 or more and less than 90 mol%, preferably 1 It is in the range of ⁇ 80 mol%, more preferably 5 to 80 mol%, most preferably 15 to 75 mol%.
- Examples of such a propylene polymer include Mitsui Chemicals, Inc .: trade name: Toughmer XM-7070.
- propylene polymer (B) When a propylene homopolymer is used as the propylene polymer (B), it is preferably a low crystalline polypropylene satisfying the following (A) to (f).
- (A) [mmmm] 20 to 60 mol%:
- the mesopentad fraction [mmmm] is preferably 30 to 50 mol%, more preferably 40 to 50 mol%.
- the mesopentad fraction [mmmm], the racemic pentad fraction [rrrr] and the racemic mesoraced mesopendad fraction [rmrm], which will be described later, are described in “Macromolecules, 6, 925 (1973)” by A. Zambelli et al.
- the mesopentad fraction [mmmm] increases, the stereoregularity increases.
- triad fractions [mm], [rr] and [mr] described later were also calculated by the above method.
- the 13 C-NMR spectrum can be measured by the following apparatus and conditions in accordance with the assignment of peaks proposed by “Macromolecules, 8, 687 (1975)” by A. Zambelli et al. it can.
- Apparatus JNM-EX400 type 13C-NMR apparatus manufactured by JEOL Ltd., Method: Proton complete decoupling method, Concentration: 220 mg / ml, Solvent: 90:10 (volume ratio) mixed solvent of 1,2,4-trichlorobenzene and heavy benzene, Temperature: 130 ° C Pulse width: 45 °, Pulse repetition time: 4 seconds, Integration: 10,000 times.
- M m / S ⁇ 100
- R ⁇ / S ⁇ 100
- S P ⁇ + P ⁇ + P ⁇
- S signal strength of side chain methyl carbon atoms of all propylene units, P ⁇ : 19.8-22.5 ppm, P ⁇ : 18.0 to 17.5 ppm, P ⁇ : 17.5 to 17.1 ppm, ⁇ : racemic pentad chain: 20.7 to 20.3 ppm, m: Mesopentad chain: 21.7-22.5 ppm.
- [rrrr] / (1- [mmmm]) is 0.1 or less, stickiness in the resulting elastic nonwoven fabric is suppressed.
- [rrrr] / (1- [mmmm]) is preferably 0.05 or less, more preferably 0.04 or less.
- the upper limit is usually about 10 mol%.
- Mass average molecular weight (Mw) 10,000 to 200,000: If the weight average molecular weight of the low crystalline polypropylene is 10,000 or more, the low crystalline polypropylene has an appropriate viscosity without being too low, so that yarn breakage during the production of the elastic nonwoven fabric is suppressed. Further, when the mass average molecular weight is 200,000 or less, the viscosity of the low crystalline polypropylene is not too high, and the spinnability is improved.
- the mass average molecular weight is preferably 30,000 to 150,000, more preferably 50,000 to 150,000. A method for measuring this mass average molecular weight will be described later.
- the mass average molecular weight (Mw) is a polystyrene-reduced mass average molecular weight measured by the gel permeation chromatography (GPC) method under the following apparatus and conditions, and the molecular weight distribution (Mw / Mn) is the same. It is a value calculated from the measured number average molecular weight (Mn) and the mass average molecular weight (Mw).
- ⁇ GPC measurement device Column: TOSO GMHHR-H (S) HT, Detector: RI detector for liquid chromatogram WATERS 150C, ⁇ Measurement conditions> Solvent: 1,2,4-trichlorobenzene, Measurement temperature: 145 ° C Flow rate: 1.0 ml / min, Sample concentration: 2.2 mg / ml, Injection volume: 160 ⁇ l, Calibration curve: Universal Calibration, Analysis program: HT-GPC (Ver. 1.0).
- the low crystalline polypropylene used in the present invention preferably further satisfies the following (g).
- G Using a differential scanning calorimeter (DSC), observed at the highest temperature side of the melting endotherm curve obtained by holding at ⁇ 10 ° C. for 5 minutes in a nitrogen atmosphere and then raising the temperature at 10 ° C./min.
- the melting point (Tm-D) defined as the peak top of the peak is 0 to 120 ° C.
- the melting point (Tm-D) of the low crystalline polypropylene is 0 ° C. or higher, stickiness of the elastic nonwoven fabric is suppressed, and when it is 120 ° C. or lower, sufficient elastic recovery is obtained.
- the melting point (Tm-D) is more preferably 0 to 100 ° C.
- the melting point (Tm-D) was determined by using a differential scanning calorimeter (manufactured by Perkin Elmer, DSC-7) and holding 10 mg of a sample at ⁇ 10 ° C. for 5 minutes in a nitrogen atmosphere, then 10 ° C./min. It can be determined as the peak top of the peak observed on the highest temperature side of the melting endothermic curve obtained by raising the temperature at.
- Such a low crystalline polypropylene can be synthesized by using a homogeneous catalyst called a metallocene catalyst as described in, for example, WO2003 / 087172.
- Examples of the low crystalline polypropylene described above include Idemitsu Kosan Co., Ltd .: trade name L-MODU S901, and Idemitsu Kosan Co., Ltd .: trade name L-MODU S600.
- the number of carbons in the present invention means the number of carbons contained in the molecule.
- palmitic acid amide (carbon number 16), stearic acid amide (carbon number 18), oleic acid amide (carbon number) 18), etc., and a plurality of these may be used in combination.
- -CONH constituting amide is also included in the carbon number.
- the number of carbon atoms of the fatty acid amide is more preferably 5 or more and 19 or less.
- oleic acid amide is particularly preferable.
- a nonwoven fabric excellent in flexibility, touch and strength can be obtained.
- the lubricant may include known ones, including fatty acid compounds, paraffin and hydrocarbon resins, silicone compounds, silicone polymers, fluorine compounds, tetrafluoroethylene and propylene. Examples thereof include a copolymer, a fluoropolymer such as a copolymer of vinylidene fluoride and hexafluoropropylene, and a mixture thereof.
- the propylene polymer composition as a raw material for the spunbonded nonwoven fabric according to the present invention contains, as essential components, a propylene polymer (A) having a melting point of 120 ° C. or higher and a fatty acid amide having 15 to 21 carbon atoms.
- the propylene polymer composition is composed of a propylene polymer (A) having a melting point of 120 ° C. or more and a propylene polymer having a melting point of less than 120 ° C. ( B) for a total of 100 parts by weight, Propylene polymer (A) having a melting point of 120 ° C. or higher: 70 to 99.9 parts by weight, The propylene polymer (B) having a melting point of less than 120 ° C .: 30 to 0.1 parts by weight, and further, the propylene polymer (A) having a melting point of 120 ° C.
- the propylene polymer (B) having a melting point of less than 120 ° C. is preferably composed of 25 to 1 part by weight, more preferably the propylene polymer (A) having a melting point of 120 ° C. or more: 80 to 97 parts by weight, Propylene polymer (B) having a melting point of less than 120 ° C .: 20 to 3 parts by weight.
- those containing the propylene polymer (A) and the propylene polymer (B) can be combined with a specific fatty acid amide to obtain a nonwoven fabric excellent in flexibility, touch and strength. .
- the fatty acid amide having 15 to 21 carbon atoms 0.01 to 1 part by weight, preferably 0.05, per 100 parts by weight in total of the propylene polymer (A) and the propylene polymer (B). Desirably, it is contained in the range of ⁇ 0.60 parts by weight, more preferably 0.10 to 0.40 parts by weight. Even if the fatty acid amide is excessively contained, the strength may be lowered or the static friction coefficient may be excessively reduced. Moreover, when there are few fatty acid amides, a softness
- the melt flow rate (MFR: ASTM D-1238, 190 ° C., load 2160 g) of the composition thus prepared is usually 1 to 150 g / 10 minutes, more preferably 10 to 100 g / 10 minutes, still more preferably 30 to 90 g. / 10 min.
- Production of Propylene Polymer Composition When producing the nonwoven fabric of the present invention, the propylene polymer (A) and a fatty acid amide having 15 to 21 carbon atoms and, if necessary, a melting point of less than 120 ° C. It is preferable to knead the propylene polymer (B) to produce a propylene polymer resin composition, and then spin it using the propylene polymer composition to form a nonwoven fabric.
- the propylene-based polymer composition is prepared by mixing various components in the above-described range by various known methods such as a multistage polymerization method, a Henschel mixer, a V-blender, a ribbon blender, a tumbler blender, or the like. Thereafter, it can be produced by a method of granulating or pulverizing after melt-kneading with a single screw extruder, twin screw extruder, kneader, Banbury mixer or the like.
- an organic peroxide or the like may be added as a decomposition accelerator (degra) if necessary for the purpose of ensuring moldability according to the nonwoven fabric production method.
- a decomposition accelerator degraving agent
- the propylene polymer composition of the present invention includes a weather resistance stabilizer, a heat resistance stabilizer, an anti-slip agent, an anti-blocking agent, an antifogging agent, a pigment, a dye, a plasticizer, and an aging as long as the object of the present invention is not impaired.
- Additives such as an inhibitor, a hydrochloric acid absorbent, an antioxidant, and a hydrophilizing agent may be blended as necessary. Further, other polymers and the like can be blended within a range that does not impair the object of the present invention without departing from the gist of the present invention.
- Producing nonwoven spunbond method from propylene polymer comprising the composition of propylene-based resin composition preparation was prepared as described above nonwoven fabric. The spunbond method is disclosed in Japanese Patent Application Laid-Open Nos. 2007-46224, 2002-317372, 2003-302862, and 2001-355172 by the applicant of the present application.
- the diameter of the fibers constituting the nonwoven fabric is generally about 0.1 to 100 ⁇ m.
- relatively thin fibers for example, 10 ⁇ m or less
- relatively thick fibers for example, thicker than 10 ⁇ m
- the spunbond method usually consists of continuous fibers.
- a nonwoven fabric By forming entanglement in the fibers formed as described above, a nonwoven fabric can be obtained.
- entanglement processing by means such as needle punching, water jet, ultrasonic sealing, or heat fusion processing by a hot embossing roll can be performed.
- a method of forming an entanglement by heat fusion treatment with a hot embossing roll is advantageous.
- the embossing area ratio of the embossing roll is appropriately determined, but is usually 5 to 30%.
- the non-woven fabric according to the present invention has a smooth feeling and a fluffy feeling, is difficult to fluff, and is extremely excellent in flexibility.
- the bending resistance of the nonwoven fabric is usually 37 or less, preferably 35 or less, more preferably 31 or less.
- the nonwoven fabric of the present invention usually has a basis weight (mass per unit area of the nonwoven fabric) of 3 to 100 g / m 2 , preferably 7 to 60 g / m 2 .
- the fiber constituting the nonwoven fabric of the present invention may be, for example, a monocomponent type, a core-sheath type, a split type, a sea-island type, or a side-by-side type composite fiber.
- a resin that forms part of the fiber May be the composition of the present invention.
- a cross-sectional shape of a fiber various well-known cross-sectional shapes, such as a round shape and a square shape, can be taken.
- the nonwoven fabric of the present invention may be a mixture of two or more types of fibers. In this case, at least one type of fiber may be the composition of the present invention.
- Nonwoven Fabric Laminate The nonwoven fabric of the present invention (hereinafter sometimes referred to as “flexible nonwoven fabric” in order to be distinguished from a normal nonwoven fabric) is obtained by laminating with various layers depending on the application.
- a knitted fabric, a woven fabric, a non-woven fabric, a film, and the like can be given.
- thermal embossing thermal fusion methods such as ultrasonic fusion
- mechanical entanglement methods such as needle punch and water jet
- hot melt adhesive urethane type
- Various known methods such as a method using an adhesive such as an adhesive, extrusion lamination, and the like can be adopted.
- nonwoven fabric laminated with the flexible nonwoven fabric examples include various known nonwoven fabrics such as a spunbond nonwoven fabric, a melt blown nonwoven fabric, a wet nonwoven fabric, a dry nonwoven fabric, a dry pulp nonwoven fabric, a flash spun nonwoven fabric, and a spread nonwoven fabric.
- the material constituting the nonwoven fabric examples include various known thermoplastic resins, for example, ⁇ -olefins such as ethylene, propylene, 1-butene, 1-hexene, 4-methyl-1-pentene and 1-octene.
- ⁇ -olefins such as ethylene, propylene, 1-butene, 1-hexene, 4-methyl-1-pentene and 1-octene.
- High-pressure low-density polyethylene linear low-density polyethylene (so-called LLDPE), high-density polyethylene, polypropylene, polypropylene random copolymer, poly-1-butene, poly-4-methyl-1-pentene, ethylene / propylene random Polyolefins such as copolymers, ethylene / 1-butene random copolymers, propylene / 1-butene random copolymers, polyesters (polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate
- the laminated body with a spun bond nonwoven fabric and / or a melt blown nonwoven fabric is mentioned.
- two layers such as spunbond nonwoven fabric / flexible nonwoven fabric, meltblown nonwoven fabric / flexible nonwoven fabric, flexible nonwoven fabric / spunbond nonwoven fabric / flexible nonwoven fabric, flexible nonwoven fabric / spunbond nonwoven fabric / meltblown nonwoven fabric, spunbond nonwoven fabric / meltblown nonwoven fabric / flexible 3 layers of non-woven fabric, flexible non-woven fabric / melt blown non-woven fabric / flexible non-woven fabric, etc., or a laminate of 4 layers or more such as flexible non-woven fabric / spunbond non-woven fabric / melt blown non-woven fabric / spun bond non-woven fabric, flexible non-woven fabric / spunbond non-woven fabric / melt blown non-woven fabric / flexible non-woven fabric Is mentioned.
- the basis weight of the nonwoven fabric of each layer to be laminated is preferably in the range of 2 to 25 g / m 2 .
- the spunbonded nonwoven fabric composed of the ultrafine fibers can be obtained by controlling (selecting) the production conditions of the spunbond method.
- Such a nonwoven fabric laminate is a laminate that takes advantage of the flexibility of the flexible nonwoven fabric of the present invention, is excellent in surface smoothness, and has improved water resistance and processability.
- the film laminated with the flexible nonwoven fabric of the present invention is preferably a breathable (moisture permeable) film that takes advantage of the breathability characteristic of the flexible nonwoven fabric of the present invention.
- a breathable film include various known breathable films, for example, films made of thermoplastic elastomers such as moisture-permeable polyurethane elastomers, polyester elastomers, polyamide elastomers, and thermoplastic resins containing inorganic or organic fine particles. Examples thereof include a porous film formed by stretching a film to be porous.
- thermoplastic resin used for the porous film is preferably a polyolefin such as high-pressure method low-density polyethylene, linear low-density polyethylene (so-called LLDPE), high-density polyethylene, polypropylene, polypropylene random copolymer, or a composition thereof.
- a polyolefin such as high-pressure method low-density polyethylene, linear low-density polyethylene (so-called LLDPE), high-density polyethylene, polypropylene, polypropylene random copolymer, or a composition thereof.
- a laminate with a breathable film can be a cross-like composite material that takes advantage of the bulkiness and flexibility of the flexible nonwoven fabric of the present invention and has extremely high water resistance.
- the nonwoven fabric of the present invention is rich in flexibility, and various medical films or sheets such as various sanitary materials, disposable diapers, sanitary products, absorbent articles, disposable masks, bansoukou, patching agents, disposable surgical gowns, rescue gowns, etc. , Medical gowns, surgical caps, disposable caps and the like.
- Nonwoven fabric of the present invention has excellent flexibility, by utilizing this flexibility, specifically, in a deployable disposable diaper or a pants-type disposable diaper, a top sheet, a back sheet, a waistband ( (Extension tape, side flap), fastening tape, three-dimensional gather, leg cuff, and part of a side panel of a pants-type disposable diaper. Good tactile sensation can be obtained by using the product of the present invention at these sites.
- a deployable disposable diaper or a pants-type disposable diaper a top sheet, a back sheet, a waistband (Extension tape, side flap), fastening tape, three-dimensional gather, leg cuff, and part of a side panel of a pants-type disposable diaper.
- Good tactile sensation can be obtained by using the product of the present invention at these sites.
- the disposable mask is generally composed of a mouth periphery covering portion and ear hook portions extending from both sides of the covering portion.
- a good touch is required.
- the nonwoven fabric of the present invention has a good tactile sensation, it is possible to satisfy these requirements by using it as an ear hook part of a disposable mask.
- Substrates used in bansoukou, patch adhesive plasters, etc. have been required to have sufficient breathability so as not to cause rashes on the skin and flexibility that does not cause a feeling of stiffness. Since the nonwoven fabric of this invention has a softness
- Disposable surgical gowns Disposable surgical gowns, rescue gowns Disposable surgical gowns, rescue gowns, etc. Arms, elbows, shoulders, sleeves and other movable indirect parts are required to be breathable and flexible.
- the non-woven fabric of the present invention is suitably used as a material used for such disposable surgical gowns and rescue gowns because it is a non-woven fabric as well as a normal non-woven fabric and has air permeability and has excellent flexibility.
- the nonwoven fabric of the present invention is a polypropylene-based nonwoven fabric excellent in flexibility, and can be used for various uses as a nonwoven fabric including sanitary materials.
- diapers and sanitary napkins are able to retain the body's movements and are non-woven, so they are breathable. Can provide particularly excellent performance.
- Thickness [ ⁇ m] Five test pieces of 100 mm (MD) ⁇ 100 mm (CD) were collected from the nonwoven fabric. In addition, the collection place was arbitrary three places. Next, the thickness [ ⁇ m] was measured by the method described in JIS L 1096 using a load-type thickness meter (manufactured by Ozaki Seisakusho) for each collected specimen. The average value of the thickness of each test piece was obtained, and the first decimal place was rounded to the thickness [ ⁇ m] of each nonwoven fabric sample.
- CD strength [N / 25mm] Five pieces of 25 mm (MD) ⁇ 200 mm (CD) CD test pieces were collected from the nonwoven fabric. In addition, the sampling place was arbitrary five places. Next, each collected specimen was pulled using a universal tensile tester (IM-201, manufactured by Intesco) under the conditions of a chuck distance of 100 mm and a tensile speed of 100 mm / min, and the maximum load [N] was measured. The average value of the CD strength of each test piece was obtained, and the second decimal place was rounded off to obtain the CD strength [N / 25 mm] of each nonwoven fabric sample.
- IM-201 universal tensile tester
- the fuzzing state of the friction surface was graded according to the following criteria, and the worse grade was designated as the fuzz [point] of each nonwoven fabric sample.
- First grade The fiber is peeled off as the specimen is broken.
- Second grade As the specimen becomes thinner, the fibers are severely peeled off.
- Grade 2.5 Hairballs are large and clearly visible, and fibers begin to float at multiple locations.
- 3rd grade A clear hairball starts to appear, or several small hairballs are seen.
- Grade 3.5 Fluffy enough to start producing small pills in one place.
- Grade 4 No fuzz.
- Tactile feeling 20 panelists confirmed the touch of the nonwoven fabric and evaluated it according to the following criteria.
- test pieces of 2 cm ⁇ 15 cm were collected from the sample in the vertical direction and the horizontal direction, respectively.
- the short side of the test piece was placed on the scale base line on a smooth horizontal platform with a 45-degree slope at one end.
- the test piece was gently slid in the direction of the slope by an appropriate method, and the position of the other end was read with a scale when the central point of one end of the test piece was in contact with the slope.
- the bending resistance is indicated by the length (mm) that the test piece has moved.
- Each of the five specimens is measured, the average value in the vertical direction (MD) and the horizontal direction (CD) is obtained, and the following formula is used. The obtained numerical value was calculated by rounding off the second decimal place.
- a single screw extruder was used as the extruder, the resin temperature and the die temperature were both 220 ° C., and the cold air temperature was 20 ° C. At that time, the spinning speed was 2750 m / min.
- the long fibers obtained by melt spinning are deposited on the collecting surface to form a nonwoven fabric, and then peeled off from the collecting surface.
- the embossed pattern has an area ratio of 6.7% and an embossed area of 0.19 mm 2.
- the spunbonded nonwoven fabric was obtained by heat bonding with heated embossing at 130 ° C. and a linear pressure of 60 kg / cm. Basis weight of the resulting spunbonded nonwoven fabric was 13.8 g / m 2.
- the obtained spunbonded nonwoven fabric was evaluated by the method described above. The evaluation results are shown in Table 1.
- Example 2 A spunbonded nonwoven fabric was collected by the same method as in Example 1 except that C1 was 0.30 part by weight, and evaluated by the method described above. The evaluation results are shown in Table 1.
- Example 3 A1: 90 parts by weight, propylene polymer (manufactured by Idemitsu Kosan Co., Ltd .: trade name L-MODU S901; melting point: 75 ° C., MFR (measured at 230 ° C., load 2.16 kg according to ASTM D1238): 80 g / 10 min.
- B1 abbreviated as “B1”.
- a composition obtained by adding 0.30 part by weight of C1 to 100 parts by weight of the A1 / B1 mixture is used.
- a spunbond nonwoven fabric was collected in the same manner as in Example 1 and evaluated by the method described above. The evaluation results are shown in Table 1.
- Example 4 A spunbonded nonwoven fabric was collected by the same method as in Example 3 except that the mixing ratio of A1 and B1 was 80 parts by weight: 20 parts by weight, and evaluated by the method described above. The evaluation results are shown in Table 1.
- Example 5 A1: 90 parts by weight, propylene polymer (manufactured by Idemitsu Kosan Co., Ltd .: trade name L-MODU S600; melting point: 70 ° C., MFR (measured at 230 ° C., load 2.16 kg according to ASTM D1238): 300 g / 10 minutes, hereinafter abbreviated as “B2”): After mixing 10 parts by weight, a composition obtained by adding 0.30 part by weight of C1 to 100 parts by weight of the A1 / B2 mixture was used. A spunbond nonwoven fabric was collected in the same manner as in Example 1 and evaluated by the method described above. The evaluation results are shown in Table 1.
- Example 6 A1: 90 parts by weight and a propylene polymer (manufactured by Mitsui Chemicals, Inc .: trade name: TAFMER XM-7070; melting point: 75 ° C., MFR (measured at 230 ° C., load 2.16 kg according to ASTM D1238): 7 g / 10 minutes (hereinafter abbreviated as “B3”): After mixing 10 parts by weight, a composition obtained by adding 0.30 part by weight of C1 to 100 parts by weight of the A1 / B3 mixture is used. A spunbonded nonwoven fabric was collected in the same manner as in Example 1 and evaluated by the method described above. The evaluation results are shown in Table 2.
- Example 7 A spunbonded nonwoven fabric was collected by the same method as in Example 6 except that the mixing ratio of A1 and B3 was 80 parts by weight: 20 parts by weight, and evaluated by the method described above. The evaluation results are shown in Table 2.
- Example 8 A1: 80 parts by weight and a propylene polymer (manufactured by ExxonMobil: trade name Vistamaxx VM2125; melting point: 160 ° C., MFR (measured at 230 ° C. under a load of 2.16 kg according to ASTM D1238): 60 g / 10 minutes.
- A2 After mixing 20 parts by weight, a composition obtained by adding 0.30 part by weight of C1 to 100 parts by weight of the A1 / A2 mixture was used. Spunbond nonwoven fabrics were collected by the same method and evaluated by the method described above. The evaluation results are shown in Table 2.
- Comparative Example 2 A spunbonded nonwoven fabric was collected by the same method as in Comparative Example 1 except that C2 was 0.30 part by weight, and evaluated by the method described above. The evaluation results are shown in Table 3.
- the nonwoven fabric according to the present invention was excellent in tactile sensation, hardly fuzzed, had a well-balanced static friction coefficient and strength, and was excellent in flexibility and bending resistance.
- the spunbonded nonwoven fabric of the present invention is suitably used for various textile products such as disposable diapers, sanitary products, sanitary products, clothing materials, bandages and packaging materials.
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Abstract
Description
[1]融点が120℃以上のプロピレン系重合体(A)と、炭素数15以上21以下の脂肪酸アミドとを含む、プロピレン系重合体組成物からなるスパンボンド不織布。
[2]炭素数15以上21以下の脂肪酸アミドが、オレイン酸アミドである[1]のスパンボンド不織布。
[3]プロピレン系重合体組成物が、さらに、融点が120℃未満のプロピレン系重合体(B)を含む、[1]または[2]のスパンボンド不織布。
[4]プロピレン系重合体組成物が、融点が120℃以上のプロピレン系重合体(A)と融点が120℃未満のプロピレン系重合体(B)の合計100重量部に対して、
融点が120℃以上のプロピレン系重合体(A):70~99.9重量部、
融点が120℃未満のプロピレン系重合体(B):30~0.1重量部であり、
炭素数15以上21以下の脂肪酸アミド:0.01~1重量部の範囲にある、[3]のスパンボンド不織布。
[5]融点が120℃未満のプロピレン系重合体(B)が、プロピレン単独重合体、または、プロピレンと、炭素数が4~20のα・オレフィンからなるランダム共重合体である[1]~[3]のスパンボンド不織布。
[6]融点が120℃未満のプロピレン系重合体(B)が、プロピレンと、炭素数が4~20のα・オレフィンからなる共重合体である、[5]のスパンボンド不織布。
[7]前記共重合体中のα・オレフィン含量が、0.1以上90モル%未満である、[6]のスパンボンド不織布。
[8]融点が120℃未満のプロピレン系重合体(B)が、
以下の(A)~(f)を満たす低結晶性ポリプロピレンである、[3]~[7]のスパンボンド不織布;
(A)[mmmm]=20~60モル%
(B)[rrrr]/(1-[mmmm])≦0.1
(c)[rmrm]>2.5モル%
(d)[mm]×[rr]/[mr]2≦2.0
(e)質量平均分子量(Mw)=10,000~200,000
(f)分子量分布(Mw/Mn)<4
[9]融点が120℃以上のプロピレン系重合体(A)が、プロピレン単独重合体、または、プロピレンとα・オレフィンからなるランダム共重合体である、[1]~[4]のスパンボンド不織布。
[10]融点が120℃以上のプロピレン系重合体(A)として、プロピレン単独重合体と、プロピレンとαオレフィンからなるランダム共重合体とを含む、[1]~[4]のスパンボンド不織布。
[11]前記[1]~[10]のスパンボンド不織布を含む、不織布積層体。
[12]前記[1]~[10]のスパンボンド不織布を用いた吸収物品。
本発明のスパンボンド不織布を形成するプロピレン系重合体(A)は、示差走査熱量計で測定される融点が120℃以上、好ましくは120~170℃を有するものである。本発明に係るプロピレン系重合体(A)は、結晶性を有し、アイソタクチック・インデックスI.I.(沸騰n-ヘプタン不溶成分)が、好ましくは75重量%以上、より好ましくは75~99重量%のポリプロピレンを用いることが望ましい。
<融点が120℃未満のプロピレン系重合体(B)>
本発明で使用されるプロピレン系重合体(B)は、融点が120℃未満のプロピレン系重合体であり、プロピレン単独重合体であっても、プロピレンと炭素原子数2または4~20のα-オレフィンとの共重合体であってもよい。このうち、本発明では、プロピレン単独重合体あるいは、プロピレンと炭素原子数4~20のα-オレフィンとの共重合体が好ましい。
低結晶性ポリプロピレンのメソペンタッド分率[mmmm]が20モル%以上であると、べたつきの発生が抑制され、60モル%以下であると、結晶化度が高くなりすぎることがないので、弾性回復性が良好となる。このメソペンタッド分率[mmmm]は、好ましくは30~50モル%、より好ましくは40~50モル%である。
装置:日本電子(株)製JNM-EX400型13C-NMR装置、
方法:プロトン完全デカップリング法、
濃度:220mg/ml、
溶媒:1,2,4-トリクロロベンゼンと重ベンゼンの90:10(容量比)混合溶媒、
温度:130℃、
パルス幅:45°、
パルス繰り返し時間:4秒、
積算:10000回。
<計算式>
M=m/S×100、
R=γ/S×100、
S=Pββ+Pαβ+Pαγ、
S:全プロピレン単位の側鎖メチル炭素原子のシグナル強度、
Pββ:19.8~22.5ppm、
Pαβ:18.0~17.5ppm、
Pαγ:17.5~17.1ppm、
γ:ラセミペンタッド連鎖:20.7~20.3ppm、
m:メソペンタッド連鎖:21.7~22.5ppm。
(B)[rrrr]/(1-[mmmm])≦0.1:
[rrrr]/[1-mmmm]の値は、上記のペンタッド単位の分率から求められ、
本発明に係る低結晶性ポリプロピレンの規則性分布の均一さを示す指標である。この値が大きくなると、既存触媒系を用いて製造される従来のポリプロピレンのように高規則性ポリプロピレンとアタクチックポリプロピレンの混合物となり、べたつきの原因となる。
(c)[rmrm]>2.5モル%:
低結晶性ポリプロピレンのラセミメソラセミメソ分率[rmrm]が2.5モル%を超える値であると、該低結晶性ポリプロピレンのランダム性が増加し、弾性不織布の弾性回復性がさらに向上する。[rmrm]は、好ましくは2.6モル%以上、より好ましくは2.7モル%以上である。その上限は、通常10モル%程度である。
(d)[mm]×[rr]/[mr]2≦2.0:
[mm]×[rr]/[mr]2は、低結晶性ポリプロピレンのランダム性の指標を示し、この値が2.0以下であると、弾性不織布は十分な弾性回復性が得られ、かつべたつきも抑制される。[mm]×[rr]/[mr]2は、0.25に近いほどランダム性が高くなる。上記十分な弾性回復性を得る観点から、[mm]×[rr]/[mr]2は、好ましくは0.25を超え1.8以下、より好ましくは0.5~1.5である。
(e)質量平均分子量(Mw)=10,000~200,000:
低結晶性ポリプロピレンにおいて質量平均分子量が10,000以上であると、該低結晶性ポリプロピレンの粘度が低すぎず適度のものとなるため、弾性不織布の製造時の糸切れが抑制される。また、質量平均分子量が200,000以下であると、上記低結晶性ポリプロピレンの粘度が高すぎず、紡糸性が向上する。この質量平均分子量は、好ましくは30,000~150,000であり、より好ましくは50,000~150,000である。この質量平均分子量の測定法については後述する。
(f)分子量分布(Mw/Mn)<4:
低結晶性ポリプロピレンにおいて、分子量分布(Mw/Mn)が4未満であると、弾性不織布のべたつきの発生が抑制される。この分子量分布は、好ましくは3以下である。 上記質量平均分子量(Mw)は、ゲルパーミエイションクロマトグラフィ(GPC)法により、下記の装置及び条件で測定したポリスチレン換算の質量平均分子量であり、上記分子量分布(Mw/Mn)は、同様にして測定した数平均分子量(Mn)及び上記質量平均分子量(Mw)より算出した値である。
<GPC測定装置>
カラム :TOSO GMHHR-H(S)HT、
検出器 :液体クロマトグラム用RI検出器 WATERS 150C、
<測定条件>
溶媒 :1,2,4-トリクロロベンゼン、
測定温度 :145℃、
流速 :1.0ml/分、
試料濃度 :2.2mg/ml、
注入量 :160μl、
検量線 :Universal Calibration、
解析プログラム:HT-GPC(Ver.1.0)。
(g)示差走査型熱量計(DSC)を用いて、窒素雰囲気下-10℃で5分間保持した後10℃/分で昇温させることにより得られた融解吸熱カーブの最も高温側に観測されるピークのピークトップとして定義される融点(Tm-D)が0~120℃である。
<炭素数15以上21以下の脂肪酸アミド>
本発明で使用される炭素数15以上21以下の脂肪酸アミドとしては、脂肪酸モノアミド化合物、脂肪酸ジアミド化合物、飽和脂肪酸モノアミド化合物、不飽和脂肪酸ジアミド化合物が挙げられる。なお、本発明における炭素数とは、分子中に含まれる炭素数を意味し、具体的には、パルミチン酸アミド(炭素数16)、ステアリン酸アミド(炭素数18)、オレイン酸アミド(炭素数18)、などが挙げられ、これらは複数組み合わせて用いることもできる。なお、アミドを構成する-CONHも炭素数に含める。脂肪酸アミドの炭素数は、より好ましくは5以上19以下である。
本発明に係るスパンボンド不織布の原料となるプロピレン系重合体組成物は、融点が120℃以上のプロピレン系重合体(A)と炭素数15以上21以下の脂肪酸アミドとを必須成分として含む。
融点が120℃以上のプロピレン系重合体(A):70~99.9重量部、
融点が120℃未満のプロピレン系重合体(B):30~0.1重量部であり、さらには
融点が120℃以上のプロピレン系重合体(A):75~99重量部、
融点が120℃未満のプロピレン系重合体(B):25~1重量部からなることが好ましく、より好ましくは
融点が120℃以上のプロピレン系重合体(A):80~97重量部、
融点が120℃未満のプロピレン系重合体(B):20~3重量部である。
プロピレン系重合体組成物の製造
本発明の不織布を製造するに際しては、予めプロピレン系重合体(A)および炭素数15以上21以下の脂肪酸アミド、および、必要に応じて、融点が120℃未満のプロピレン系重合体(B)とを混練してプロピレン系重合体樹脂組成物を製造した後に、このプロピレン系重合体組成物を用いて紡糸して不織布に成形するのが好ましい。ここでプロピレン系重合体組成物は、各成分を上記のような範囲で種々公知の方法、たとえば、多段重合法、ヘンシェルミキサー、V-ブレンダー、リボンブレンダー、タンブラブレンダー等で混合する方法、あるいは混合後、一軸押出機、二軸押出機、ニーダー、バンバリーミキサー等で溶融混練後、造粒あるいは粉砕する方法を採用して製造することができる。
プロピレン系重合体組成物からなる不織布の製法
上記のようにして調製されたプロピレン系樹脂組成物からスパンボンド法で不織布を製造する。スパンボンド法については、本願出願人による、特開2007-46224号公報、特開2002-317372号公報、特開2003-302862号公報、特開2001-355172号公報に開示されている。
不織布
上記のようにして得られる本発明の不織布は、特定の組成物から構成されるので、静摩擦係数が、0.41~0.8の範囲にある。
不織布積層体
本発明の不織布(以下、通常の不織布と区別するために、「柔軟不織布」と呼ぶ場合がある。)は、用途により種々の層と積層して得る。
吸収性物品
使い捨ておむつあるいは生理用品等の吸収性物品は、風合いや良好な触感が求められる。本発明の不織布は優れた柔軟性を有しているので、この柔軟性を利用して、具体的には、展開型使い捨ておむつあるいはパンツ型使い捨ておむつには、トップシート、バックシート、ウェストバンド(延長テープ、サイドフラップ)、ファスニングテープ、立体ギャザー、レッグカフ、またパンツ型使い捨ておむつのサイドパネル等の部位に好適に用いることができる。これら部位に本発明品を使用することで、良好な触感を得ることが可能となる。
使い捨てマスク
使い捨てマスクは一般に、口許周辺被覆部と、前記被覆部の両側から延びる耳掛け部から構成されている。マスク着用中には、特に耳掛け部が着用者の顔面に接触するため、良好な肌触りが求められる。本発明の不織布は良好な触感を有しているので、使い捨てマスクの耳掛け部に使用することでこれら要求を満足することが可能となる。
バンソウコウ、貼布剤
絆創膏等に用いられる基材には、肌にかぶれを起こさないための充分な通気性、ごわごわ感を感じさせない柔軟性が要求されてきた。本発明の不織布は、柔軟性を有するとともに、通気性を有するため、これら絆創膏等に用いられる基材として好適に使用される。
使い捨て手術着、レスキューガウン
使い捨て手術着、レスキューガウンなどの腕、肘、肩、袖など可動間接部には通気性、柔軟性が求められる。本発明の不織布は、通常の不織布と同様に不織布であるため通気性を有し、更に優れた柔軟性を有するためこれら使い捨て手術着、レスキューガウンなどに用いられる素材として好適に使用される。
不織布から100mm(MD)×100mm(CD)の試験片を5点採取した。なお、採取場所は任意の5箇所とした。次いで、採取した各試験片に対して上皿電子天秤(研精工業社製)を用いて、それぞれ質量(g)を測定した。各試験片の質量の平均値を求めた。求めた平均値から1m2当たりの質量(g)に換算し、小数点第2位を四捨五入して各不織布サンプルの目付〔g/m2〕とした。
不織布から100mm(MD)×100mm(CD)の試験片を5点採取した。なお、採取場所は任意の3箇所とした。次いで、採取した各試験片に対して荷重型厚み計(尾崎製作所社製)を用いて、JIS L 1096に記載の方法で厚み〔μm〕を測定した。各試験片の厚みの平均値を求め、小数点第1位を四捨五入して各不織布サンプルの厚み〔μm〕とした。
不織布から10mm(MD)×10mm(CD)の試験片を5点採取した。なお、採取場所は任意の1箇所とした。次いで、試験片を光学顕微鏡を用いて倍率200倍で撮影し、その画像を画像寸法計測ソフトウェア(イノテック社製:Pixs2000 Version2.0)により解析した。各試験片について10本の繊維径を測定し、各試験片の繊維径の平均値を求め、小数点第2位を四捨五入して各不織布サンプルの繊維径〔μm〕とした。
不織布から150mm(MD)×150mm(CD)の試験片を2点採取した。なお、採取場所は任意の2箇所とした。次いで、試験片をカトーテック(株)製のKES-FBシステムにより、測定条件としてニット高感度条件にて圧縮試験を行い、LC値〔-〕を測定した。各試験片のLC値の平均値を求め、小数点第3位を四捨五入して各不織布サンプルのLC値〔-〕とした。LC値はその数値が小さいほど、厚み辺りの初期圧縮仕事が小さく、柔軟性に優れることを示す。
不織布から300mm(MD)×100mm(CD)の試験片と100mm(MD)×100mm(CD)の試験片を各3点採取した。なお、採取場所は任意の各3箇所(計6箇所)とした。次いで、JIS K 7125に準拠し100mm(MD)×100mm(CD)の試験片を、エンボス面を外側になるように滑り片へ貼付し、300mm(MD)×100mm(CD)の試験片をエンボス面が摩擦されるように試験テーブルに貼付し、両試験片のエンボス面同士の静摩擦係数〔-〕を測定した。各試験片の静摩擦係数の平均値を求め、小数点第3位を四捨五入して各不織布サンプルの静摩擦係数〔-〕とした。
不織布から25mm(MD)×200mm(CD)のCD試験片を各5点採取した。なお、採取場所は任意の5箇所とした。次いで、採取した各試験片を万能引張試験機(インテスコ社製、IM-201型)を用いて、チャック間100mm、引張速度100mm/minの条件にて引っ張り、最大荷重〔N〕を測定した。各試験片のCD強度の平均値を求め、小数点第2位を四捨五入して各不織布サンプルのCD強度〔N/25mm〕とした。
不織布から150mm(MD)×150mm(CD)のCD試験片を各2点採取した。なお、採取場所は任意の2箇所とした。次いで、採取した各試験片を学振型摩擦堅牢度試験機(大栄科学精器製作所社製、新型NR-100)を用い、JIS L 0849の摩擦堅牢度試験法に準拠して摩擦試験を行った。なお、摩擦子側には布テープ(寺岡製作所社製、No.1532)を貼付し、荷重300gをかけた状態で、非エンボス面をMD方向に50回往復させて擦り、各試験片における被摩擦面の毛羽立ち状態を以下の基準で等級づけ、等級の悪い方を各不織布サンプルの毛羽立ち〔点〕とした。
1級:試験片が破損するほど繊維が剥ぎ取られる。
2級:試験片が薄くなるほど甚だしく繊維が剥ぎ取られている。
2.5級:毛玉が大きくはっきり見られ、複数箇所で繊維が浮き上がりはじめる。
3級:はっきりとした毛玉ができはじめ、または小さな毛玉が複数見られる。
3.5級:一カ所に小さな毛玉ができはじめる程度に毛羽立っている。
4級:毛羽立ちがない。
パネラー20人が不織布の手触りを確認し、下記基準で評価した。
A:20人のうち20人が柔らかいと感じた場合。
B:20人のうち19~15人が柔らかいと感じた場合。
C:20人のうち14~10人が柔らかいと感じた場合。
D:20人のうち9~5人が柔らかいと感じた場合。
E:20人のうち4~0人が柔らかいと感じた場合。
(9)剛軟度(カンチレバー法)
JIS1096の8.19.1[A法(45°カンチレバー法)]に準拠した。
剛軟度 = {(MDの平均値^2+CDの平均値^2)/2}^(1/2)
[実施例1]
結晶性PP(株式会社プライムポリマー社製:商品名 プライムポリプロ S119;融点:156℃、MFR(ASTM D1238に準拠し、温度230℃、荷重2.16kgで測定):62g/10分。以下、「A1」と略す。):100重量部に対してオレイン酸アミド(以下、「C1」と略す。)を0.15重量部添加してなる組成物を用い、スパンボンド法により溶融紡糸を行った。
C1を0.30重量部とした以外は、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表1に示す。
A1:90重量部と、プロピレン重合体(出光興産株式会社製:商品名 L-MODU S901;融点:75℃、MFR(ASTM D1238に準拠し、温度230℃、荷重2.16kgで測定):80g/10分。以下、「B1」と略す。):10重量部とを、混合した後、A1/B1混合物100重量部に対してC1を0.30重量部添加してなる組成物を用い、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表1に示す。
A1とB1との混合比を80重量部:20重量部とした以外は、実施例3と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表1に示す。
A1:90重量部と、プロピレン重合体(出光興産株式会社製:商品名 L-MODU S600;融点:70℃、MFR(ASTM D1238に準拠し、温度230℃、荷重2.16kgで測定):300g/10分。以下、「B2」と略す。):10重量部とを、混合した後、A1/B2混合物100重量部に対してC1を0.30重量部添加してなる組成物を用い、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表1に示す。
A1:90重量部と、プロピレン系重合体(三井化学株式会社製:商品名 タフマー XM-7070;融点:75℃、MFR(ASTM D1238に準拠し、温度230℃、荷重2.16kgで測定):7g/10分。以下、「B3」と略す。):10重量部とを、混合した後、A1/B3混合物100重量部に対してC1を0.30重量部添加してなる組成物を用い、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方
法で評価した。評価結果を表2に示す。
A1とB3との混合比を80重量部:20重量部とした以外は、実施例6と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表2に示す。
A1:80重量部と、プロピレン重合体(ExxonMobil社製:商品名 Vistamaxx VM2125;融点:160℃、MFR(ASTM D1238に準拠し、温度230℃、荷重2.16kgで測定):60g/10分。以下、「A2」と略す。):20重量部とを、混合した後、A1/A2混合物100重量部に対してC1を0.30重量部添加してなる組成物を用い、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表2に示す。
A1を100重量部に対してエルカ酸アミド(以下、「C2」と略す。)を0.15重量部添加してなる組成物を用い、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表3に示す。
C2を0.30重量部とした以外は、比較例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表3に示す。
C2を0.45重量部とした以外は、比較例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表3に示す。
A1:90重量部と、B1:10重量部とを混合した後、A1/B1混合物100重量部に対してC2を0.30重量部添加してなる組成物を用い、実施例1と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表3に示す。
比較例4で用いたB1をB2に替えた以外は、比較例4と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表3に示す。
比較例4で用いたB1をB3に替えた以外は、比較例4と同様の方法でスパンボンド不織布を採取し、上記記載の方法で評価した。評価結果を表3に示す。
Claims (12)
- 融点が120℃以上のプロピレン系重合体(A)と、炭素数15以上21以下の脂肪酸アミドとを含む、プロピレン系重合体組成物からなるスパンボンド不織布。
- 炭素数15以上21以下の脂肪酸アミドが、オレイン酸アミドである請求項1記載のスパンボンド不織布。
- プロピレン系重合体組成物が、さらに、融点が120℃未満のプロピレン系重合体(B)を含む、請求項1または2に記載のスパンボンド不織布。
- プロピレン系重合体組成物は、融点が120℃以上のプロピレン系重合体(A)と融点が120℃未満のプロピレン系重合体(B)の合計100重量部に対して、
融点が120℃以上のプロピレン系重合体(A):70~99.9重量部、
融点が120℃未満のプロピレン系重合体(B):30~0.1重量部であり、
炭素数15以上21以下の脂肪酸アミド:0.01~1重量部の範囲にある、
請求項3に記載のスパンボンド不織布。 - 融点が120℃未満のプロピレン系重合体(B)が、プロピレン単独重合体、または、プロピレンと、炭素数が4~20のα・オレフィンからなるランダム共重合体である請求項1~3のいずれかに記載のスパンボンド不織布。
- 融点が120℃未満のプロピレン系重合体(B)が、プロピレンと、炭素数が4~20のα・オレフィンからなる共重合体である、請求項5に記載のスパンボンド不織布。
- 前記共重合体中のα・オレフィン含量が、0.1以上90モル%未満である、請求項6に記載のスパンボンド不織布。
- 融点が120℃未満のプロピレン系重合体(B)が、以下の(a)~(f)を満たす低結晶性ポリプロピレンである、請求項3~7のいずれかに記載のスパンボンド不織布;
(a)[mmmm]=20~60モル%
(b)[rrrr]/(1-[mmmm])≦0.1
(c)[rmrm]>2.5モル%
(d)[mm]×[rr]/[mr]2≦2.0
(e)質量平均分子量(Mw)=10,000~200,000
(f)分子量分布(Mw/Mn)<4 - 融点が120℃以上のプロピレン系重合体(A)が、プロピレン単独重合体、または、プロピレンとα・オレフィンからなるランダム共重合体である請求項1~4のいずれかに記載のスパンボンド不織布。
- 融点が120℃以上のプロピレン系重合体(A)として、プロピレン単独重合体と、プロピレンとαオレフィンからなるランダム共重合体とを含む、請求項1~4のいずれかに記載のスパンボンド不織布。
- 請求項1~10のいずれかに記載のスパンボンド不織布を含む、不織布積層体。
- 請求項1~10のいずれかに記載のスパンボンド不織布を用いた吸収物品。
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WO2017006972A1 (ja) * | 2015-07-06 | 2017-01-12 | 三井化学株式会社 | スパンボンド不織布及び衛生材料 |
JPWO2017006972A1 (ja) * | 2015-07-06 | 2018-03-15 | 三井化学株式会社 | スパンボンド不織布及び衛生材料 |
US20180213852A1 (en) * | 2015-07-06 | 2018-08-02 | Mitsui Chemicals, Inc. | Spunbond nonwoven fabric and hygienic material |
JP2017179658A (ja) * | 2016-03-30 | 2017-10-05 | 三井化学株式会社 | スパンボンド不織布および衛生材料 |
WO2019146656A1 (ja) | 2018-01-24 | 2019-08-01 | 三井化学株式会社 | スパンボンド不織布、衛生材料、及びスパンボンド不織布の製造方法 |
WO2020095947A1 (ja) * | 2018-11-09 | 2020-05-14 | 出光興産株式会社 | 不織布及びその製造方法 |
WO2020158875A1 (ja) | 2019-01-30 | 2020-08-06 | 三井化学株式会社 | スパンボンド不織布、衛生材料、及びスパンボンド不織布の製造方法 |
JPWO2020158875A1 (ja) * | 2019-01-30 | 2021-12-02 | 三井化学株式会社 | スパンボンド不織布、衛生材料、及びスパンボンド不織布の製造方法 |
JP7138197B2 (ja) | 2019-01-30 | 2022-09-15 | 三井化学株式会社 | スパンボンド不織布、衛生材料、及びスパンボンド不織布の製造方法 |
US11702779B2 (en) | 2019-01-30 | 2023-07-18 | Mitsui Chemicals, Inc. | Spunbonded non-woven fabric, sanitary material, and method of manufacturing spunbonded non-woven fabric |
Also Published As
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DK2902538T3 (en) | 2018-04-30 |
EP2902538A1 (en) | 2015-08-05 |
EP2902538A4 (en) | 2016-06-29 |
JPWO2014050965A1 (ja) | 2016-08-22 |
CN104662218A (zh) | 2015-05-27 |
MY180806A (en) | 2020-12-09 |
US20150233031A1 (en) | 2015-08-20 |
KR20150046334A (ko) | 2015-04-29 |
CN104662218B (zh) | 2017-07-14 |
EP2902538B1 (en) | 2018-03-07 |
KR101720442B1 (ko) | 2017-03-27 |
JP5931207B2 (ja) | 2016-06-08 |
TW201416504A (zh) | 2014-05-01 |
TWI601858B (zh) | 2017-10-11 |
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