TWI770366B - Spunbond Nonwoven - Google Patents
Spunbond Nonwoven Download PDFInfo
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- TWI770366B TWI770366B TW108106677A TW108106677A TWI770366B TW I770366 B TWI770366 B TW I770366B TW 108106677 A TW108106677 A TW 108106677A TW 108106677 A TW108106677 A TW 108106677A TW I770366 B TWI770366 B TW I770366B
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- nonwoven fabric
- spunbond nonwoven
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- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 166
- 239000000835 fiber Substances 0.000 claims abstract description 144
- 238000000034 method Methods 0.000 claims abstract description 67
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 39
- 239000006185 dispersion Substances 0.000 claims abstract description 25
- 230000003746 surface roughness Effects 0.000 claims abstract description 22
- 150000001875 compounds Chemical class 0.000 claims description 24
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 22
- 229930195729 fatty acid Natural products 0.000 claims description 22
- 239000000194 fatty acid Substances 0.000 claims description 22
- 150000004665 fatty acids Chemical class 0.000 claims description 22
- 239000000155 melt Substances 0.000 claims description 9
- 229920005673 polypropylene based resin Polymers 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 abstract description 6
- 238000009987 spinning Methods 0.000 description 63
- -1 ester compound Chemical class 0.000 description 34
- 229920005989 resin Polymers 0.000 description 21
- 239000011347 resin Substances 0.000 description 21
- 238000004049 embossing Methods 0.000 description 19
- 239000000463 material Substances 0.000 description 18
- 239000004743 Polypropylene Substances 0.000 description 16
- 229920001155 polypropylene Polymers 0.000 description 16
- 238000002844 melting Methods 0.000 description 13
- 230000008018 melting Effects 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 238000012360 testing method Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 10
- 229920001519 homopolymer Polymers 0.000 description 10
- 238000005259 measurement Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 239000012748 slip agent Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- ZJOLCKGSXLIVAA-UHFFFAOYSA-N ethene;octadecanamide Chemical compound C=C.CCCCCCCCCCCCCCCCCC(N)=O.CCCCCCCCCCCCCCCCCC(N)=O ZJOLCKGSXLIVAA-UHFFFAOYSA-N 0.000 description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- ULNRTPCFRBIMKL-GHVJWSGMSA-N (e)-2-tetracosenoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCC\C=C\C(O)=O ULNRTPCFRBIMKL-GHVJWSGMSA-N 0.000 description 1
- ZVUNTIMPQCQCAQ-UHFFFAOYSA-N 2-dodecanoyloxyethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCC ZVUNTIMPQCQCAQ-UHFFFAOYSA-N 0.000 description 1
- PIFNLEVPOVXBCF-UHFFFAOYSA-N CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O Chemical compound CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O.CCCC=CC(N)=O PIFNLEVPOVXBCF-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- 229920001875 Ebonite Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- GWHCXVQVJPWHRF-UHFFFAOYSA-N cis-tetracosenoic acid Natural products CCCCCCCCC=CCCCCCCCCCCCCCC(O)=O GWHCXVQVJPWHRF-UHFFFAOYSA-N 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- BZLPNQQVFAFIBI-UHFFFAOYSA-N dodecanoyloxymethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCOC(=O)CCCCCCCCCCC BZLPNQQVFAFIBI-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical class [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- 229940072106 hydroxystearate Drugs 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- MYSPBSKLIFPWDI-UHFFFAOYSA-N octacosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(N)=O MYSPBSKLIFPWDI-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000004439 roughness measurement Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/005—Synthetic yarns or filaments
- D04H3/007—Addition polymers
-
- D—TEXTILES; PAPER
- 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
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
- D04H3/16—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nonwoven Fabrics (AREA)
Abstract
本發明提供一種紡黏不織布,其包含雖然平均單纖維直徑為細徑但是紡絲性良好且生產性高的聚烯烴系纖維,質地均勻,表面光滑且手感、肌膚觸感優異,更具有高柔軟性。本發明係關於一種紡黏不織布,其係由包含聚烯烴系樹脂的纖維所構成之紡黏不織布,其中前述纖維之平均單纖維直徑為6.5~11.9μm,根據反射光亮度之纖維分散度為10以下,且至少單面之根據KES法之表面粗糙度SMD為1.0~2.6μm。 The present invention provides a spunbond nonwoven fabric comprising polyolefin-based fibers with good spinnability and high productivity despite a small average single fiber diameter, uniform texture, smooth surface, excellent hand and skin feel, and high softness sex. The present invention relates to a spunbond nonwoven fabric, which is a spunbond nonwoven fabric composed of fibers containing polyolefin resin, wherein the average single fiber diameter of the aforementioned fibers is 6.5-11.9 μm, and the fiber dispersion degree according to the reflected light brightness is 10 Hereinafter, the surface roughness SMD according to the KES method on at least one side is 1.0 to 2.6 μm.
Description
本發明係關於一種紡黏不織布,其係由包含聚烯烴系樹脂的纖維所構成,特別適合作為衛生材料用途之使用。 The present invention relates to a spunbond nonwoven fabric, which is composed of fibers containing polyolefin resin, and is particularly suitable for use as a sanitary material.
一般而言,對於紙尿布或衛生棉等的衛生材料用之不織布,要求手感、肌膚觸感、柔軟性及高生產性。特別地,由於紙尿布的頂面薄片係直接接觸肌膚的材料,故為對於肌膚觸感、柔軟性之要求高的用途之一。 In general, nonwoven fabrics for sanitary materials such as disposable diapers and sanitary napkins are required to have a feel, feel, softness, and high productivity. In particular, since the top sheet of a disposable diaper is a material that directly contacts the skin, it is one of the applications requiring high skin touch and softness.
如此,作為提升手感、肌膚觸感及柔軟性之手段,向來已知控制構成不織布的纖維之纖維直徑之手法為有效果的。例如,有提案藉由將纖維的纖度與吸附力設為特定之範圍,而提升纖維本身的彎曲柔軟度之紡黏不織布(參照專利文獻1)。 As described above, it has been known that the method of controlling the fiber diameter of the fibers constituting the nonwoven fabric is effective as a means for improving the texture, skin feel, and softness. For example, there is proposed a spunbond nonwoven fabric in which the flexural softness of the fiber itself is improved by setting the fineness and the adsorption force of the fiber in a specific range (see Patent Document 1).
又,有提案藉由使用熔體流動速率比較大的聚丙烯系樹脂作為原料,將牽伸比設為1500以上,而將單纖維纖度細徑化到1.5丹尼以下,兼顧柔軟性與強度之方法(參照專利文獻2)。 In addition, there is a proposal to use a polypropylene-based resin with a relatively high melt flow rate as a raw material, set the draft ratio to 1500 or more, and reduce the single fiber fineness to 1.5 denier or less to achieve both flexibility and strength. method (refer to Patent Document 2).
專利文獻1:日本特開2013-159884號公報 Patent Document 1: Japanese Patent Laid-Open No. 2013-159884
專利文獻2:日本發明專利第4943349號公報 Patent Document 2: Japanese Invention Patent No. 4943349
然而,於專利文獻1所揭示之方法中,使用熔體流動速率比較小,即高黏度之聚丙烯系樹脂作為原料,藉由將紡絲速度高速化為如5,000m/分鐘,而將纖維予以細徑化,故容易發生斷線,難以安定地生產。 However, in the method disclosed in Patent Document 1, a polypropylene-based resin having a relatively low melt flow rate, that is, a high viscosity, is used as a raw material, and the spinning speed is increased to, for example, 5,000 m/min. As the diameter is reduced, wire breakage is likely to occur, making it difficult to produce stably.
再者,於專利文獻1中,亦顯示藉由含有具有70℃以上的熔點之酯化合物,而將光滑感賦予不織布,提升肌膚觸感。然而,於此提案中雖然的確摩擦係數降低,但是若對照所要求的水準,則不織布之光滑度無法令人充分滿足,而要求肌膚觸感的進一步提升。 Furthermore, in Patent Document 1, it is also shown that by containing an ester compound having a melting point of 70° C. or higher, a smooth feeling is imparted to a nonwoven fabric, and the skin feel is improved. However, although the friction coefficient is indeed reduced in this proposal, the smoothness of the non-woven fabric cannot be sufficiently satisfied when compared to the required level, and further improvement of the skin feel is required.
另一方面,於專利文獻2所揭示之方法中,藉由使用熔體流動速率比較大的聚丙烯系樹脂作為原料,將牽伸比設為1500以上而進行細徑化,故必須以大孔徑的紡嘴將低黏度的原料予以紡絲。因此,難以施加紡嘴背壓,無法均勻地紡出,有容易發生斷線、纖維直徑不均之課題,另外在質地均勻性亦有改善之餘地。 On the other hand, in the method disclosed in Patent Document 2, by using a polypropylene-based resin having a relatively large melt flow rate as a raw material, and making the draft ratio 1500 or more, the diameter is reduced, so it is necessary to use a large pore diameter The spinning nozzle spins low-viscosity raw materials. Therefore, it is difficult to apply the back pressure of the spinning nozzle, and the spinning cannot be uniform, and there are problems that thread breakage and uneven fiber diameter are likely to occur, and there is room for improvement in the uniformity of the texture.
因此,鑒於上述課題,本發明之目的在於提供一種紡黏不織布,其包含雖然平均單纖維直徑為細徑但是紡絲性良好且生產性高的聚烯烴系纖維,質地均勻,表面光滑且手感、肌膚觸感優異,更具有高柔軟性。 Therefore, in view of the above-mentioned problems, an object of the present invention is to provide a spunbond nonwoven fabric comprising polyolefin-based fibers with good spinnability and high productivity although the average single fiber diameter is small, and which has a uniform texture, a smooth surface, and a feel, Excellent skin feel and high softness.
本發明之紡黏不織布為一種紡黏不織布,其係由包含聚烯烴系樹脂的纖維所構成之紡黏不織布,前述纖維之平均單纖維直徑為6.5~11.9μm,根據反射光亮度之纖維分散度為10以下,且至少單面之根據KES法之表面粗糙度SMD為1.0~2.6μm。 The spunbond nonwoven fabric of the present invention is a spunbond nonwoven fabric, which is a spunbond nonwoven fabric composed of fibers containing polyolefin resin, the average single fiber diameter of the aforementioned fibers is 6.5~11.9 μm, and the fiber dispersion degree according to the reflected light brightness It is 10 or less, and the surface roughness SMD by KES method of at least one side is 1.0-2.6 micrometers.
若根據本發明之紡黏不織布的較佳態樣,則前述紡黏不織布之表觀密度為0.05~0.3g/cm3。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the apparent density of the aforementioned spunbond nonwoven fabric is 0.05-0.3 g/cm 3 .
若根據本發明之紡黏不織布的較佳態樣,則前述紡黏不織布的至少單面之根據KES法之平均摩擦係數MIU為0.1~0.5。 According to a preferred aspect of the spunbond nonwoven fabric according to the present invention, the average friction coefficient MIU of at least one side of the spunbond nonwoven fabric according to the KES method is 0.1 to 0.5.
若根據本發明之紡黏不織布的較佳態樣,則前述紡黏不織布之根據KES法之平均摩擦係數之變動MMD為0.008以下。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the variation MMD of the average friction coefficient of the spunbond nonwoven fabric according to the KES method is 0.008 or less.
若根據本發明之紡黏不織布的較佳態樣,則前述紡黏不織布之熔體流動速率為155~850g/10分鐘。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the melt flow rate of the aforementioned spunbond nonwoven fabric is 155-850 g/10 minutes.
若根據本發明之紡黏不織布的較佳態樣,則係使前述聚烯烴系樹脂中含有碳數23以上50以下的脂肪酸醯胺化合物。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the polyolefin-based resin contains a fatty acid amide compound having 23 to 50 carbon atoms.
若根據本發明之紡黏不織布的較佳態樣,則前述脂肪酸醯胺化合物之添加量為0.01~5.0質量%。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the amount of the fatty acid amide compound added is 0.01 to 5.0% by mass.
若根據本發明之紡黏不織布的較佳態樣,則前述脂肪酸醯胺化合物為伸乙基雙硬脂酸醯胺。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the aforementioned fatty acid amide compound is ethylene bisstearate.
若根據本發明之紡黏不織布的較佳態樣,則前述紡黏不織布係藉由包含聚丙烯系樹脂的纖維構成而成。 According to a preferred aspect of the spunbond nonwoven fabric of the present invention, the aforementioned spunbond nonwoven fabric is formed of fibers containing polypropylene-based resin.
若根據本發明,可得到一種紡黏不織布,其包含雖然平均單纖維直徑為細徑但是紡絲性良好且生產性高的聚烯烴纖維,質地均勻,表面光滑且手感、肌膚觸感優異,更具有高柔軟性。由於此等特性,本發明之紡黏不織布特別可適用作為衛生材料用途。 According to the present invention, it is possible to obtain a spunbond nonwoven fabric comprising polyolefin fibers having good spinnability and high productivity although the average single fiber diameter is small, having a uniform texture, a smooth surface, excellent hand and skin feel, and more Has high flexibility. Due to these characteristics, the spunbond nonwoven fabric of the present invention is particularly suitable for use as a sanitary material.
本發明之紡黏不織布為一種紡黏不織布,其係由包含聚烯烴系樹脂的纖維所構成之紡黏不織布,前述纖維之平均單纖維直徑為6.5~11.9μm,根據反射光亮度之纖維分散度為10以下,且至少單面之根據KES法(Kawabata Evaluation System,川端評估系統)之表面粗糙度SMD為1.0~2.6μm。 The spunbond nonwoven fabric of the present invention is a spunbond nonwoven fabric, which is a spunbond nonwoven fabric composed of fibers containing polyolefin resin, the average single fiber diameter of the aforementioned fibers is 6.5~11.9 μm, and the fiber dispersion degree according to the reflected light brightness It is 10 or less, and the surface roughness SMD according to KES method (Kawabata Evaluation System, Kawabata Evaluation System) of at least one side is 1.0~2.6 μm.
藉由成為如此,可作成質地均勻,表面光滑且粗糙感小,手感、肌膚觸感優異,且柔軟性優異之紡黏不織布。以下,說明此等之詳細。 By doing so, a spunbond nonwoven fabric having a uniform texture, a smooth surface, little roughness, excellent hand and skin feel, and excellent softness can be produced. The details of these will be described below.
關於本發明所用之聚烯烴系樹脂,例如可舉出聚丙烯系樹脂及聚乙烯系樹脂。 As a polyolefin resin used for this invention, a polypropylene resin and a polyethylene resin are mentioned, for example.
作為聚丙烯系樹脂,例如可舉出丙烯的均聚物、或者丙烯與各種α-烯烴之共聚物等。 Examples of polypropylene-based resins include homopolymers of propylene, copolymers of propylene and various α-olefins, and the like.
又,作為聚乙烯系樹脂,例如可舉出乙烯的均聚物、或者乙烯與各種α-烯烴之共聚物等。 Moreover, as a polyethylene-type resin, the homopolymer of ethylene, the copolymer of ethylene and various alpha-olefin, etc. are mentioned, for example.
從紡絲性、強度的特性之觀點來看,特佳使用聚丙烯系樹脂。 From the viewpoint of spinnability and strength characteristics, polypropylene-based resins are particularly preferably used.
關於本發明所用之聚烯烴系樹脂,丙烯的均聚物之比例較佳為60質量%以上,更佳為70質量%以上,進一步較佳為80質量%以上。藉由設為上述範圍,可維持良好的紡絲性,且提升強度。 Regarding the polyolefin-based resin used in the present invention, the ratio of the homopolymer of propylene is preferably 60% by mass or more, more preferably 70% by mass or more, and still more preferably 80% by mass or more. By setting it as the said range, favorable spinnability can be maintained, and intensity|strength can be improved.
作為本發明所用之聚烯烴系樹脂,可為2種以上之混合物,而且也可使用含有其它的烯烴系樹脂或熱塑性彈性體等之樹脂組成物。 As the polyolefin-based resin used in the present invention, a mixture of two or more kinds may be used, and a resin composition containing other olefin-based resins, thermoplastic elastomers, and the like may also be used.
又,亦可作為組合有上述聚烯烴系樹脂的複合型纖維使用。作為複合型纖維之複合形態,例如可舉出同心芯鞘型、偏心芯鞘型及海島型等的複合形態。其中,從紡絲性優異,可藉由熱接著而使纖維彼此均勻地接著來看,較佳的態樣為作成同心芯鞘型的複合形態。 Moreover, it can also be used as a composite fiber in which the above-mentioned polyolefin resin is combined. Examples of the composite form of the composite fiber include a concentric core-sheath type, an eccentric core-sheath type, and a sea-island type. Among them, from the viewpoint of being excellent in spinnability and being able to uniformly bond fibers to each other by thermal bonding, a preferred aspect is a composite form of a concentric core-sheath type.
於本發明所用之聚烯烴系樹脂中,在不損害本發明的效果之範圍內,因應需要可添加通常使用的抗氧化劑、耐候安定劑、耐光安定劑、抗靜電劑、防霧劑、防沾黏劑(antiblocking agent)、助滑劑、成核劑及顏料等之添加物、或其它的聚合物。 In the polyolefin resin used in the present invention, within the scope of not impairing the effect of the present invention, commonly used antioxidants, weather-resistant stabilizers, light-resistant stabilizers, antistatic agents, antifogging agents, anti-staining agents can be added as required. Additives such as antiblocking agents, slip agents, nucleating agents and pigments, or other polymers.
本發明所用之聚烯烴系樹脂的熔點較佳為80~200℃,更佳為100~180℃,進一步較佳為120~180℃。藉由將熔點較佳設為80℃以上,更佳設為100℃以上,進一步較佳設為120℃以上,變得容易得到耐得 住實用的耐熱性。又,藉由將熔點較佳設為200℃以下,更佳設為180℃以下,變得容易將從紡嘴所吐出的紗線冷卻,抑制纖維彼此的熔接而變得容易進行安定的紡絲。 The melting point of the polyolefin resin used in the present invention is preferably 80 to 200°C, more preferably 100 to 180°C, and further preferably 120 to 180°C. By setting the melting point to preferably be 80°C or higher, more preferably 100°C or higher, and further preferably 120°C or higher, it becomes easy to obtain heat resistance that can withstand practical use. In addition, by making the melting point preferably 200° C. or lower, more preferably 180° C. or lower, it becomes easy to cool the yarn discharged from the spinning nozzle, suppresses fusion of fibers, and facilitates stable spinning. .
本發明之紡黏不織布的原料之聚烯烴系樹脂的熔體流動速率(以下,有時記載為MFR)較佳為155~850g/10分鐘,更佳為155~600g/10分鐘,進一步較佳為155~400g/10分鐘。 The melt flow rate (hereinafter, sometimes referred to as MFR) of the polyolefin resin as the raw material of the spunbond nonwoven fabric of the present invention is preferably 155 to 850 g/10 minutes, more preferably 155 to 600 g/10 minutes, still more preferably It is 155~400g/10 minutes.
此聚烯烴系樹脂的MFR係採用藉由ASTM D1238(A法)所測定之值。 The MFR of this polyolefin resin adopts the value measured by ASTM D1238 (A method).
另外,若根據此規格,則例如聚丙烯係規定在荷重:2.16kg、溫度:230℃下測定;聚乙烯係規定在荷重:2.16kg、溫度:190℃下測定。 In addition, according to this standard, for example, polypropylene type is prescribed under load: 2.16 kg, temperature: 230°C, and polyethylene type is prescribed under load: 2.16 kg, temperature: 190°C.
當然,亦可以任意之比例摻合MFR不同的2種類以上之樹脂,而調整聚烯烴系樹脂的MFR。此時,對於主要的聚烯烴系樹脂所摻合的樹脂之MFR,較佳為10~1000g/10分鐘,更佳為20~800g/10分鐘,進一步較佳為30~600g/10分鐘。藉由設為上述範圍,可防止在所摻合的聚烯烴系樹脂中部分地發生黏度不均且纖度不均勻化、或者紡絲性變差。 Of course, it is also possible to adjust the MFR of the polyolefin-based resin by blending two or more types of resins having different MFRs in an arbitrary ratio. At this time, the MFR of the resin blended with the main polyolefin-based resin is preferably 10 to 1000 g/10 minutes, more preferably 20 to 800 g/10 minutes, and still more preferably 30 to 600 g/10 minutes. By setting it as the said range, the nonuniformity of viscosity and the nonuniformity of fineness, or the deterioration of spinnability can be prevented from partially generating in the polyolefin resin to be blended.
又,於後述之紡出纖維時,為了防止發生部分的黏度不均,將纖維的纖度均勻化,進一步如後述細化纖維直徑,而亦考慮對於所用的樹脂,分解該樹脂而調整MFR。然而,例如較佳為不添加過氧化物、尤其是二烷基過氧化物等的游離自由基劑等。使用此手法時,除了部分地發生黏度不均而纖度不均勻化,變得難以充 分地細化纖維直徑之外,亦有因黏度不均或分解氣體所造成的氣泡而紡絲性變差之情況。 In addition, in order to prevent the occurrence of partial viscosity unevenness during the spinning of fibers, the fineness of the fibers is made uniform, and the fiber diameter is further reduced as described later. The resin used is also considered to be decomposed to adjust the MFR. However, for example, it is preferable not to add a free radical agent such as a peroxide, especially a dialkyl peroxide or the like. When this method is used, in addition to the unevenness of the viscosity and the unevenness of the fineness, it becomes difficult to sufficiently thin the fiber diameter, and the spinnability is also deteriorated due to the unevenness of the viscosity or the bubbles caused by the decomposed gas. Happening.
於本發明之紡黏不織布,為了提升滑動性、柔軟性,較佳的態樣係使相當於構成纖維之包含聚烯烴系樹脂的聚烯烴系纖維中,含有碳數為23以上50以下的脂肪酸醯胺化合物。 In the spunbond nonwoven fabric of the present invention, in order to improve the sliding property and the softness, a preferable aspect is that the polyolefin-based fiber corresponding to the polyolefin-based resin constituting the fiber contains a fatty acid having a carbon number of 23 to 50. amide compounds.
藉由將混合於聚烯烴系樹脂中的脂肪酸醯胺化合物之碳數較佳設為23以上,更佳設為30以上,可抑制脂肪酸醯胺化合物過度地露出纖維表面,作成紡絲性與加工安定性優異者,保持高生產性。另一方面,藉由將脂肪酸醯胺化合物之碳數較佳設為50以下,更佳設為42以下,而脂肪酸醯胺化合物變得容易移動至纖維表面,可將滑動性與柔軟性賦予紡黏不織布。 By making the carbon number of the fatty acid amide compound mixed in the polyolefin resin preferably 23 or more, more preferably 30 or more, the fatty acid amide compound can be suppressed from being excessively exposed on the fiber surface, and the spinnability and processing can be achieved. Those with excellent stability maintain high productivity. On the other hand, by making the carbon number of the fatty acid amide compound preferably 50 or less, more preferably 42 or less, the fatty acid amide compound can easily move to the surface of the fiber, and the slidability and flexibility can be imparted to the spinning Sticky nonwoven.
作為本發明所使用之碳數23以上50以下的脂肪酸醯胺化合物,例如可舉出飽和脂肪酸單醯胺化合物、飽和脂肪酸二醯胺化合物、不飽和脂肪酸單醯胺化合物及不飽和脂肪酸二醯胺化合物等。 Examples of fatty acid amide compounds having 23 to 50 carbon atoms used in the present invention include saturated fatty acid monoamide compounds, saturated fatty acid diamide compounds, unsaturated fatty acid monoamide compounds, and unsaturated fatty acid diamide compounds. compounds, etc.
具體而言,作為碳數23以上50以下的脂肪酸醯胺化合物,可舉出二十四酸醯胺、二十六酸醯胺、二十八酸醯胺、二十四碳烯酸醯胺、二十四碳五烯酸醯胺、二十四碳六烯酸醯胺、伸乙基雙月桂酸醯胺、亞甲基雙月桂酸醯胺、伸乙基雙硬脂酸醯胺、伸乙基雙羥基硬脂酸醯胺、伸乙基雙二十二酸醯胺、六亞甲基雙硬脂酸醯胺、六亞甲基雙二十二酸醯胺、六亞甲基羥基硬脂酸醯胺、二硬脂基己二酸醯胺、二硬脂基癸二酸醯胺、 伸乙基雙油酸醯胺、伸乙基雙芥子酸醯胺及六亞甲基雙油酸醯胺等,此等亦可複數組合而使用。 Specifically, examples of the fatty acid amide compound having 23 to 50 carbon atoms include behenic acid amide, hexadecanoic acid amide, octacosanoic acid amide, tetracosenoic acid amide, Docosapentaenoic acid amide, docosahexaenoic acid amide, ethylene bis-laurate, methylene bis-laurate, ethylene bis-stearate, ethylene ethylene Ethyl bis-hydroxystearic acid amide, ethylene bis-docosamide, hexamethylene bis-docosamide, hexamethylene bis-docosamide, hexamethylene hydroxy stearate Amide, Amide Distearyl Adipate, Amide Distearyl Sebacate, Amide Ethylene Dioleate, Amide Ethylene Dioleate, Ammonium Ethylene Dioleate and Hexamethylene Dioleate Amines, etc., these can also be used in combination in plural.
於本發明中,在此等脂肪酸醯胺化合物之中,尤其較佳使用飽和脂肪酸二醯胺化合物的伸乙基雙硬脂酸醯胺。伸乙基雙硬脂酸醯胺由於熱安定性優異而可熔融紡絲,藉由包含摻合有此伸乙基雙硬脂酸醯胺的聚烯烴系樹脂的纖維,可得到保持高生產性,並且滑動性、柔軟性優異之紡黏不織布。 In the present invention, among these fatty acid amide compounds, ethylene bisstearic acid amide, which is a saturated fatty acid diamide compound, is particularly preferably used. Ethyl ethylene bisstearate can be melt-spun due to its excellent thermal stability, and high productivity can be obtained by including a fiber containing a polyolefin-based resin blended with this ethyl bis-stearate. , and spunbond non-woven fabric with excellent sliding and softness.
於本發明中,較佳的態樣為相對於此包含聚烯烴系樹脂的纖維,脂肪酸醯胺化合物之添加量為0.01~5.0質量%。藉由將脂肪酸醯胺化合物之添加量較佳設為0.01~5.0質量%,更佳設為0.1~3.0質量%,進一步較佳設為0.1~1.0質量%,可維持紡絲性,並且賦予適度的滑動性與柔軟性。 In the present invention, a preferable aspect is that the addition amount of the fatty acid amide compound is 0.01 to 5.0 mass % with respect to the fiber containing the polyolefin-based resin. By setting the addition amount of the fatty acid amide compound to preferably 0.01 to 5.0 mass %, more preferably to 0.1 to 3.0 mass %, and further preferably to 0.1 to 1.0 mass %, spinnability can be maintained and moderate Sliding and softness.
此處所謂的添加量,係指相對於構成本發明之紡黏不織布的聚烯烴系樹脂整體所添加的脂肪酸醯胺化合物之質量百分率。例如,即使僅於構成芯鞘型複合纖維的鞘部成分中添加脂肪酸醯胺化合物時,也算出相對於芯鞘成分整體量之添加比例。 The addition amount here means the mass percentage of the fatty acid amide compound added with respect to the whole polyolefin resin which comprises the spunbond nonwoven fabric of this invention. For example, even when the fatty acid amide compound is added only to the sheath component constituting the core-sheath type conjugate fiber, the addition ratio with respect to the total amount of the core-sheath component is calculated.
作為測定相對於包含聚烯烴系樹脂的纖維之脂肪酸醯胺化合物的添加量之方法,例如可舉出將添加劑從前述纖維中進行溶劑萃取,使用液相層析質量分析(LS/MS)等進行定量分析之方法。此時,萃取溶劑係因應脂肪酸醯胺化合物之種類而適宜選擇,例如於伸乙基雙硬脂酸醯胺之情況,可舉出使用氯仿-甲醇混合液等之方 法作為一例。 As a method of measuring the addition amount of the fatty acid amide compound with respect to the fiber containing the polyolefin resin, for example, solvent extraction of the additive from the fiber, liquid chromatography mass spectrometry (LS/MS), etc. can be mentioned. Methods of quantitative analysis. At this time, the extraction solvent is appropriately selected according to the type of the fatty acid amide compound, for example, in the case of ethylene bisstearic acid amide, a method of using a chloroform-methanol mixed solution can be mentioned as an example.
構成本發明之紡黏不織布的纖維,重要的是平均單纖維直徑為6.5~11.9μm。藉由將平均單纖維直徑設為6.5μm以上,較佳設為7.5μm以上,更佳設為8.4μm以上,可防止紡絲性之降低,安定地生產品質良好的紡黏不織布。另一方面,藉由將平均單纖維直徑設為11.9μm以下,較佳設為11.2μm以下,更佳設為10.6μm以下,可提升柔軟性,且作成均勻性高的紡黏不織布。 It is important that the fibers constituting the spunbond nonwoven fabric of the present invention have an average single fiber diameter of 6.5 to 11.9 μm. By setting the average single fiber diameter to be 6.5 μm or more, preferably 7.5 μm or more, and more preferably 8.4 μm or more, a decrease in spinnability can be prevented, and a good quality spunbond nonwoven fabric can be stably produced. On the other hand, by setting the average single fiber diameter to be 11.9 μm or less, preferably 11.2 μm or less, and more preferably 10.6 μm or less, flexibility can be improved and a spunbond nonwoven fabric with high uniformity can be obtained.
另外,於本發明中,構成前述紡黏不織布的纖維之平均單纖維直徑(μm),係採用藉由以下的程序所算出之值。 In addition, in this invention, the average single fiber diameter (micrometer) of the fiber which comprises the said spunbond nonwoven fabric uses the value calculated by the following procedure.
(1)將聚烯烴系樹脂予以熔融紡絲,以噴射器(ejector)牽引‧延伸後,在網狀物(net)上捕集不織纖維網(web)。 (1) Polyolefin-based resin is melt-spun, drawn and stretched by an ejector, and then a nonwoven web (web) is collected on a net.
(2)隨機地採集小片樣品(100×100mm)10個。 (2) 10 small samples (100×100 mm) were randomly collected.
(3)以顯微鏡拍攝500~1000倍的表面照片,測定從各樣品中各10根,合計100根的聚烯烴纖維之寬度。 (3) A photograph of the surface at a magnification of 500 to 1000 is taken with a microscope, and the width of 10 polyolefin fibers in total from 10 of each sample is measured.
(4)從所測定的100根之值的平均值,算出平均單纖維直徑(μm)。 (4) From the average value of 100 measured values, the average single fiber diameter (μm) was calculated.
構成本發明之紡黏不織布的纖維,其單纖維直徑的CV值較佳為7%以下。藉由將單纖維直徑的CV值較佳設為7%以下,更佳設為6%以下,進一步較佳設為5%以下,可防止在表面產生粗糙感,作成均勻性高的 紡黏不織布。對於單纖維直徑的CV值,主要受紡絲嘴的背壓或紗冷卻條件、延伸條件的均勻性所影響,可藉由適當地調整此等而控制。 The CV value of the single fiber diameter of the fibers constituting the spunbond nonwoven fabric of the present invention is preferably 7% or less. By making the CV value of the single fiber diameter preferably 7% or less, more preferably 6% or less, and further preferably 5% or less, it is possible to prevent roughness on the surface and to produce a spunbond nonwoven fabric with high uniformity. . The CV value of the single fiber diameter is mainly affected by the back pressure of the spinneret, the yarn cooling conditions, and the uniformity of the stretching conditions, and can be controlled by appropriately adjusting these.
重要的是本發明之紡黏不織布之根據反射光亮度之纖維分散度為10以下。根據反射光亮度之纖維分散度,係表示以0.1×0.1吋的格子劃分紡黏不織布而識別時的纖維之分散程度的指標,纖維分散度愈小,纖維愈均勻地分散,成為質地均勻性優異之不織布。藉由將根據反射光亮度之纖維分散度設為10以下,較佳設為9.5以下,更佳設為9以下,可使纖維充分地開纖而將質地均勻化,防止在表面發生凹凸、或者於物性發生偏差。又,即使於紙尿布等的製程所一般使用的超音波接著中,也不發生部分的接著不良或過度接著,可安定而均勻地接著。纖維分散度可藉由適當地調整紡黏不織布的熔體流動速率、纖維之平均單纖維直徑而控制。 It is important that the spunbond nonwoven fabric of the present invention has a fiber dispersion of 10 or less in terms of reflected light brightness. According to the fiber dispersion degree of reflected light brightness, it is an index indicating the degree of fiber dispersion when the spunbond nonwoven fabric is divided into a 0.1 × 0.1 inch grid to identify the fiber dispersion degree. The smaller the fiber dispersion degree, the more uniform the fibers are. of non-woven fabrics. By setting the fiber dispersion according to the brightness of reflected light to 10 or less, preferably 9.5 or less, and more preferably 9 or less, the fibers can be sufficiently opened to make the texture uniform, and unevenness on the surface can be prevented, or Deviations from physical properties. In addition, even in the ultrasonic bonding generally used in the manufacturing process of disposable diapers and the like, partial bonding failure or excessive bonding does not occur, and stable and uniform bonding is possible. The degree of fiber dispersion can be controlled by appropriately adjusting the melt flow rate of the spunbond nonwoven fabric and the average single fiber diameter of the fibers.
另外,本發明之紡黏不織布之根據反射光亮度之纖維分散度,更詳細而言,係採用藉由以下的程序所測定之值。 In addition, the fiber dispersion degree according to the reflected light brightness of the spunbonded nonwoven fabric of the present invention, more specifically, is a value measured by the following procedure.
(1)將黏不織布貼於黑襯紙(AC Card黑#350)。 (1) Stick the non-woven fabric on the black backing paper (AC Card black #350).
(2)以全彩200dpi掃描,作成紡黏不織布的彩色掃描影像,以JPG形式保存。 (2) Scan at 200dpi in full color to make a color scanned image of spunbond non-woven fabric and save it in JPG format.
(3)從掃描影像中切出6×6吋(1200×1200像素)的影像。 (3) Cut out a 6×6 inch (1200×1200 pixel) image from the scanned image.
(4)分割成0.1×0.1吋(20×20像素)之格子單位。 (4) Divide into grid units of 0.1×0.1 inches (20×20 pixels).
(5)於各自的格子中,使用以下之式,對於各畫素算出以YUV色空間所定義的亮度之平均值(平均亮度),求出彼等的平均亮度之標準偏差。 (5) In each grid, the average value (average luminance) of luminance defined in the YUV color space is calculated for each pixel using the following formula, and the standard deviation of the average luminance is obtained.
‧(各畫素之亮度)=0.29891×R+0.58661×G+0.11448×B ‧(Brightness of each pixel)=0.29891×R+0.58661×G+0.11448×B
此處,R、G、B各自表示RGB彩色模式的紅色、綠色、藍色之亮度。 Here, R, G, and B each represent the luminance of red, green, and blue in the RGB color mode.
(6)於紡黏不織布的寬度方向等間隔地以每1m三點來進行,求出各點的標準偏差的平均值,將小數點以下第二位予以四捨五入而當作纖維分散度。 (6) Three points per 1 m are carried out at equal intervals in the width direction of the spunbond nonwoven fabric, the average value of the standard deviation of each point is obtained, and the second decimal place is rounded off to obtain the fiber dispersion degree.
本發明之紡黏不織布重要的是至少單面之根據KES法之表面粗糙度SMD為1.0~2.6μm。藉由將根據KES法之表面粗糙度SMD設為1.0μm以上,較佳設為1.3μm以上,更佳設為1.6μm以上,進一步較佳設為2.0μm以上,可防止:紡黏不織布過度地緻密化而手感變差,或者損害柔軟性。另一方面,藉由將根據KES法之表面粗糙度SMD設為2.6μm以下,較佳設為2.5μm以下,更佳設為2.4μm以下,進一步較佳設為2.3μm以下,可作成表面光滑且粗糙感小、肌膚觸感優異之紡黏不織布。根據KES法之表面粗糙度SMD,可藉由適當地調整平均單纖維直徑或單纖維直徑的CV值、纖維分散度等而控制。 It is important for the spunbonded nonwoven fabric of the present invention that the surface roughness SMD of at least one side according to the KES method is 1.0 to 2.6 μm. By setting the surface roughness SMD according to the KES method to 1.0 μm or more, preferably 1.3 μm or more, more preferably 1.6 μm or more, and still more preferably 2.0 μm or more, it is possible to prevent the spunbonded nonwoven from becoming excessively thick. Densification and poor hand feel, or softness is impaired. On the other hand, by setting the surface roughness SMD according to the KES method to 2.6 μm or less, preferably 2.5 μm or less, more preferably 2.4 μm or less, and still more preferably 2.3 μm or less, the surface can be made smooth. Spunbond non-woven fabric with less roughness and excellent skin touch. The surface roughness SMD according to the KES method can be controlled by appropriately adjusting the average single fiber diameter or the CV value of the single fiber diameter, the degree of fiber dispersion, and the like.
另外,本發明中根據KES法之表面粗糙度SMD,係採用如以下所測定的值。 In addition, in the present invention, the surface roughness SMD according to the KES method adopts the value measured as follows.
(1)於紡黏不織布的寬度方向等間隔地從紡黏不織 布採集3片寬度200mm×200mm之試驗片。 (1) Three test pieces with a width of 200 mm × 200 mm were collected from the spunbond nonwoven fabric at equal intervals in the width direction of the spunbond nonwoven fabric.
(2)將試驗片設置於試料台。 (2) The test piece is set on the sample table.
(3)以施加有10gf的荷重之表面粗糙度測定用接觸頭(材料:0.5mm鋼琴線,接觸長度:5mm),掃描試驗片之表面,測定表面的凹凸形狀之平均偏差。 (3) A contact tip for surface roughness measurement (material: 0.5mm piano wire, contact length: 5mm), scan the surface of the test piece, and measure the average deviation of the uneven shape of the surface.
(4)於全部的試驗片之縱向(不織布之長度方向)與橫向(不織布之寬度方向)進行上述之測定,將此等的合計6點之平均偏差予以平均,將小數點以下第二位予以四捨五入,當作表面粗糙度SMD(μm)。 (4) The above-mentioned measurement is carried out in the longitudinal direction (longitudinal direction of the non-woven fabric) and the transverse direction (the width direction of the non-woven fabric) of all the test pieces, the average deviation of the total of 6 points is averaged, and the second decimal place is calculated as It is rounded up as the surface roughness SMD (μm).
本發明之紡黏不織布的至少單面之根據KES法之平均摩擦係數MIU較佳為0.1~0.5。藉由將平均摩擦係數MIU較佳設為0.5以下,更佳設為0.45以下,進一步較佳設為0.4以下,可提升不織布表面的滑動性,作成使肌膚觸感更良好的紡黏不織布。另一方面,藉由將平均摩擦係數MIU較佳設為0.1以上,更佳設為0.15以上,進一步較佳設為0.2以上,可防止:過度地添加助滑劑而紡絲性變差,或者將紗線捕集在網狀物上時紗線滑動而質地變差。根據KES法之平均摩擦係數MIU,可藉由調整平均單纖維直徑或纖維分散度等,或者在聚烯烴系樹脂中添加助滑劑而控制。 The average friction coefficient MIU according to the KES method of at least one side of the spunbond nonwoven fabric of the present invention is preferably 0.1 to 0.5. By making the average friction coefficient MIU preferably 0.5 or less, more preferably 0.45 or less, and further preferably 0.4 or less, the slidability of the surface of the nonwoven fabric can be improved, and a spunbond nonwoven fabric with better skin feel can be produced. On the other hand, by making the average friction coefficient MIU preferably 0.1 or more, more preferably 0.15 or more, and still more preferably 0.2 or more, it is possible to prevent the spinnability from being deteriorated due to excessive addition of the slip agent, or When the yarn is captured on the mesh, the yarn slips and the texture becomes poor. The average friction coefficient MIU according to the KES method can be controlled by adjusting the average single fiber diameter, fiber dispersion, etc., or by adding a slip agent to the polyolefin-based resin.
本發明之紡黏不織布的至少單面之根據KES法之平均摩擦係數之變動MMD較佳為0.002~0.008。藉由將平均摩擦係數之變動MMD較佳設為0.008以下,更佳設為0.0077以下,進一步較佳設為0.0075以下,可更減低紡黏不織布的表面之粗糙感。另一方面,藉由將平 均摩擦係數之變動MMD較佳設為0.002以上,更佳設為0.004以上,進一步較佳設為0.005以上,可防止:生產設備複雜化,或者生產性極度地降低。根據KES法之平均摩擦係數之變動MMD,可藉由調整平均單纖維直徑或單纖維直徑的CV值、纖維分散度等,或者在聚烯烴系樹脂中添加助滑劑而控制。 The variation MMD of the average friction coefficient according to the KES method of at least one side of the spunbond nonwoven fabric of the present invention is preferably 0.002 to 0.008. By making the variation MMD of the average friction coefficient preferably 0.008 or less, more preferably 0.0077 or less, and still more preferably 0.0075 or less, the surface roughness of the spunbond nonwoven fabric can be further reduced. On the other hand, by making the variation MMD of the average friction coefficient preferably 0.002 or more, more preferably 0.004 or more, and still more preferably 0.005 or more, it is possible to prevent the production facility from being complicated or the productivity from being extremely lowered. The variation MMD of the average friction coefficient according to the KES method can be controlled by adjusting the average single fiber diameter or the CV value of the single fiber diameter, fiber dispersion, etc., or by adding a slip agent to the polyolefin resin.
另外,本發明中根據KES法之平均摩擦係數MIU、平均摩擦係數之變動MMD,係採用如以下所測定之值。 In the present invention, the average friction coefficient MIU and the variation MMD of the average friction coefficient according to the KES method are the values measured as follows.
(1)於紡黏不織布之寬度方向等間隔地從紡黏不織布採集3片的寬度200mm×200mm之試驗片。 (1) Three test pieces with a width of 200 mm×200 mm were collected from the spunbond nonwoven fabric at equal intervals in the width direction of the spunbond nonwoven fabric.
(2)將試驗片設置於試料台。 (2) The test piece is set on the sample table.
(3)以施加有50gf的荷重之接觸摩擦頭(材料:0.5mm鋼琴線(20條並列),接觸面積:1cm2),掃描試驗片之表面,測定平均摩擦係數。 (3) Contact the friction head with a load of 50gf (material: 0.5 mm piano wire (20 parallel), contact area: 1 cm 2 ), scan the surface of the test piece, and measure the average friction coefficient.
(4)於全部的試驗片之縱向(不織布之長度方向)與橫向(不織布之寬度方向)進行上述之測定,將此等的合計6點之平均偏差予以平均,將小數點以下第四位予以四捨五入,當作平均摩擦係數MIU。又,將前述的合計6點之平均摩擦係數之變動進一步平均,將小數點以下第四位予以四捨五入,當作平均摩擦係數之變動MMD。 (4) The above-mentioned measurement was carried out in the longitudinal direction (longitudinal direction of the non-woven fabric) and the transverse direction (the width direction of the non-woven fabric) of all the test pieces, the average deviation of the total of 6 points was averaged, and the fourth decimal place was calculated as Rounded to the nearest whole number and regarded as the average friction coefficient MIU. In addition, the fluctuation of the average friction coefficient of the above-mentioned 6 points in total was further averaged, and the fourth place below the decimal point was rounded to the nearest 5, and it was regarded as the fluctuation MMD of the average friction coefficient.
又,於本發明中,關於紡黏不織布之手感,藉由感官試驗進行評價。 Moreover, in the present invention, the texture of the spunbond nonwoven fabric was evaluated by a sensory test.
本發明之紡黏不織布的MFR較佳為155~850g/10分鐘。藉由將MFR較佳設為155~850g/10分 鐘,更佳設為155~600g/10分鐘,進一步較佳設為155~400g/10分鐘,而使纖維延伸時的細化行為安定,即使為了提高生產性而以快速的紡絲速度進行延伸,也可安定地紡絲。又,藉由使細化行為安定,而抑制紗晃動,變得不易發生捕集成片狀時的不均。再者,由於可安定地以快速的紡絲速度進行延伸,故可進行纖維的配向結晶化,作成具有高機械強度之纖維。 The MFR of the spunbond nonwoven fabric of the present invention is preferably 155-850 g/10 minutes. By setting the MFR to preferably 155 to 850 g/10 minutes, more preferably to 155 to 600 g/10 minutes, and still more preferably to be 155 to 400 g/10 minutes, the thinning behavior during fiber extension is stabilized, even if In order to improve productivity, it can be spun at a fast spinning speed, and stable spinning is also possible. In addition, by stabilizing the thinning behavior, the yarn backlash is suppressed, and unevenness at the time of capturing into a sheet becomes less likely to occur. Furthermore, since the drawing can be performed stably at a fast spinning speed, the orientation and crystallization of the fibers can be performed, and fibers having high mechanical strength can be obtained.
本發明之紡黏不織布的熔體流動速率(MFR),係採用藉由ASTM D1238(A法)所測定之值。 The melt flow rate (MFR) of the spunbonded nonwoven fabric of the present invention is the value measured by ASTM D1238 (method A).
另外,若根據此規格,則例如聚丙烯係規定在荷重:2.16kg、溫度:230℃下測定;聚乙烯係規定在荷重:2.16kg、溫度:190℃下測定。 In addition, according to this standard, for example, polypropylene type is prescribed under load: 2.16 kg, temperature: 230°C, and polyethylene type is prescribed under load: 2.16 kg, temperature: 190°C.
本發明之紡黏不織布的單位面積重量較佳為10~100g/m2。藉由將單位面積重量較佳設為10g/m2以上,更佳設為13g/m2以上,進一步較佳設為15g/m2以上,可得到可供實用的機械強度之紡黏不織布。另一方面,藉由將單、位面積重量較佳設為100g/m2以下,更佳設為50g/m2以下,進一步較佳設為30g/m2以下,可作成具有適合作為衛生材料用的不織布使用之適度柔軟性的紡黏不織布。 The weight per unit area of the spunbond nonwoven fabric of the present invention is preferably 10 to 100 g/m 2 . By making the basis weight preferably 10 g/m 2 or more, more preferably 13 g/m 2 or more, and still more preferably 15 g/m 2 or more, a spunbond nonwoven fabric with practical mechanical strength can be obtained. On the other hand, by setting the weight per unit area to preferably 100 g/m 2 or less, more preferably 50 g/m 2 or less, and still more preferably 30 g/m 2 or less, it is possible to make it suitable for use as a sanitary material. The non-woven fabric used is a moderately soft spunbond non-woven fabric.
另外,於本發明中,紡黏不織布的單位面積重量係依據JIS L1913(2010年)的「6.2每單位面積的質量」,採用藉由以下的程序所測定之值。 In addition, in this invention, the basis weight of a spunbond nonwoven fabric is based on "6.2 mass per unit area" of JIS L1913 (2010), and the value measured by the following procedure is used.
(1)於試料之寬度每1m採集3片20cm×25cm之試驗片。 (1) Collect 3 test pieces of 20cm×25cm for every 1m of the width of the sample.
(2)秤量標準狀態下的各自之質量(g)。 (2) Weigh the respective mass (g) in the standard state.
(3)以每1m2的質量(g/m2)表示其平均值。 (3) The average value is expressed in terms of mass per 1 m 2 (g/m 2 ).
本發明之紡黏不織布的厚度較佳為0.05~1.5mm。藉由將厚度較佳設為0.05~1.5mm,更佳設為0.08~1.0mm,進一步較佳設為0.10~0.8mm,而具備柔軟性與適度的緩衝性,可作成衛生材料用之紡黏不織布,尤其可作成適合於紙尿布用途使用之紡黏不織布。 The thickness of the spunbond nonwoven fabric of the present invention is preferably 0.05 to 1.5 mm. By setting the thickness to preferably 0.05~1.5mm, more preferably 0.08~1.0mm, and further preferably 0.10~0.8mm, it has softness and moderate cushioning, and can be used as a spunbond for sanitary materials Non-woven fabrics, especially spunbond non-woven fabrics suitable for use in disposable diapers.
另外,於本發明中,紡黏不織布的厚度(mm)係依據JIS L1906(2000年)的「5.1」,採用藉由以下的程序所測定之值。 In addition, in this invention, the thickness (mm) of a spunbond nonwoven fabric is based on "5.1" of JIS L1906 (2000), and the value measured by the following procedure is employ|adopted.
(1)使用直徑10mm的加壓頭,在荷重10kPa下,以0.01mm單位來測定於不織布的寬度方向等間隔地每1m十點的厚度。 (1) Using a pressure head having a diameter of 10 mm, under a load of 10 kPa, the thickness was measured at ten points per 1 m at equal intervals in the width direction of the nonwoven fabric in units of 0.01 mm.
(2)將上述十點的平均值之小數點以下第三位予以四捨五入。 (2) Round off the average of the above ten points to the third place below the decimal point.
又,本發明之紡黏不織布之表觀密度較佳為0.05~0.3g/cm3。藉由將表觀密度較佳設為0.3g/cm3以下,更佳設為0.25g/cm3以下,進一步較佳設為0.20g/cm3以下,可防止纖維緊密地填充而損害紡黏不織布的柔軟性。 In addition, the apparent density of the spunbond nonwoven fabric of the present invention is preferably 0.05 to 0.3 g/cm 3 . By setting the apparent density to preferably 0.3 g/cm 3 or less, more preferably 0.25 g/cm 3 or less, and still more preferably 0.20 g/cm 3 or less, it is possible to prevent the fibers from being densely packed and impair the spunbond. The softness of non-woven fabrics.
另一方面,藉由將表觀密度較佳設為0.05g/cm3以上,更佳設為0.08g/cm3以上,進一步較佳設為0.10g/cm3以上,可抑制起毛、層間剝離之發生,作成具備耐得住實用的強度、操作性之紡黏不織布。 On the other hand, by making the apparent density preferably 0.05 g/cm 3 or more, more preferably 0.08 g/cm 3 or more, and still more preferably 0.10 g/cm 3 or more, fuzzing and interlayer peeling can be suppressed When this happens, a spunbond nonwoven fabric with durable and practical strength and handleability is produced.
另外,於本發明中,表觀密度(g/cm3)係從上 述之四捨五入前的單位面積重量與厚度,基於下式算出,將小數點以下第三位予以四捨五入者。 In addition, in the present invention, the apparent density (g/cm 3 ) is calculated based on the following formula from the above-mentioned basis weight and thickness before rounding, and rounds off the third decimal place.
‧表觀密度(g/cm3)=[單位面積重量(g/m2)]/[厚度(mm)]×10-3。 • Apparent density (g/cm 3 )=[weight per unit area (g/m 2 )]/[thickness (mm)]×10 -3 .
本發明之紡黏不織布的硬挺度較佳為70mm以下。藉由將硬挺度較佳設為70mm以下,更佳設為67mm以下,進一步較佳設為64mm以下,作為衛生材料用之紡黏不織布,可得到尤其適合於紙尿布用途使用之適度的柔軟性。又,由於當硬挺度極度地低時,有操作性差之情況,故硬挺度較佳為10mm以上。硬挺度可藉由單位面積重量、單纖維直徑及熱壓接條件(壓接率、溫度及線壓等)而調整。 The stiffness of the spunbond nonwoven fabric of the present invention is preferably 70 mm or less. By setting the stiffness to preferably 70 mm or less, more preferably 67 mm or less, and further preferably 64 mm or less, as a spunbond nonwoven fabric for hygiene materials, it is possible to obtain moderate softness especially suitable for use in disposable diapers. . Further, when the stiffness is extremely low, the handleability may be poor, so the stiffness is preferably 10 mm or more. Stiffness can be adjusted by basis weight, single fiber diameter, and thermocompression bonding conditions (compression bonding ratio, temperature, linear pressure, etc.).
本發明之紡黏不織布之根據KES法之平均彎曲剛性B較佳為0.001~0.02gf‧cm2/cm。藉由將根據KES法之平均彎曲剛性B較佳設為0.02gf‧cm2/cm以下,更佳設為0.017gf‧cm2/cm以下,進一步較佳設為0.015gf‧cm2/cm以下,尤其在作為衛生材料用之紡黏不織布使用時,可得到充分的柔軟性。又,由於當根據KES法之平均彎曲剛性B極度地低時,有操作性差之情況,故平均彎曲剛性B較佳為0.001gf‧cm2/cm以上。根據KES法之平均彎曲剛性B可藉由單位面積重量、單纖維直徑及熱壓接條件(壓接率、溫度及線壓等)而調整。 The average bending rigidity B according to the KES method of the spunbond nonwoven fabric of the present invention is preferably 0.001 to 0.02 gf·cm 2 /cm. By setting the average bending rigidity B according to the KES method to preferably 0.02 gf·cm 2 /cm or less, more preferably 0.017 gf·cm 2 /cm or less, still more preferably 0.015 gf·cm 2 /cm or less , especially when used as a spunbond non-woven fabric for sanitary materials, sufficient softness can be obtained. Further, when the average bending rigidity B according to the KES method is extremely low, the handleability may be poor, so the average bending rigidity B is preferably 0.001 gf·cm 2 /cm or more. The average bending rigidity B according to the KES method can be adjusted by basis weight, single fiber diameter, and thermocompression bonding conditions (compression bonding ratio, temperature, linear pressure, etc.).
本發明之紡黏不織布之每單位面積重量的5%伸長時應力(以下,有時記載為每單位面積重量的5%模數)較佳為0.06~0.33(N/25mm)/(g/m2),更佳為0.13 ~0.30(N/25mm)/(g/m2),進一步較佳為0.20~0.27(N/25mm)/(g/m2)。藉由設成上述範圍,可作成保持可供實用的強度,並且柔軟且觸感優異之紡黏不織布。 The stress at 5% elongation per unit area weight of the spunbond nonwoven fabric of the present invention (hereinafter, sometimes described as 5% modulus per unit area weight) is preferably 0.06 to 0.33 (N/25mm)/(g/m 2 ), more preferably 0.13-0.30(N/25mm)/(g/m 2 ), further preferably 0.20-0.27(N/25mm)/(g/m 2 ). By setting it as the said range, the spunbond nonwoven fabric which maintains practical strength, and is soft and excellent in touch can be produced.
另外,於本發明中,紡黏不織布之每單位面積重量的5%伸長時應力,係依據JIS L1913(2010年)的「6.3拉伸強度及伸長率(ISO法)」,採用藉由以下的程序所測定之值。 In addition, in the present invention, the stress at 5% elongation per unit area weight of the spunbond nonwoven fabric is based on "6.3 Tensile strength and elongation (ISO method)" of JIS L1913 (2010), and is adopted by the following The value determined by the program.
(1)對於不織布之縱向(不織布之長度方向)與橫向(不織布之寬度方向)各自,於寬度每1m採集3片25mm×300mm之試驗片。 (1) For each of the longitudinal direction (the longitudinal direction of the non-woven fabric) and the transverse direction (the width direction of the non-woven fabric), three test pieces of 25 mm×300 mm were collected every 1 m in width.
(2)以夾具間隔200mm,將試驗片設置於拉伸試驗機。 (2) The test piece was installed in the tensile tester with a gap of 200 mm between the jigs.
(3)以拉伸速度100mm/分鐘,實施拉伸試驗,測定5%伸長時的應力(5%模數)。 (3) A tensile test was carried out at a tensile speed of 100 mm/min, and the stress (5% modulus) at 5% elongation was measured.
(4)求出於各試驗片所測定之縱向與橫向的5%模數之平均值,基於下式,算出每單位面積重量的5%模數,將小數點以下第三位予以四捨五入。 (4) Calculate the average value of the 5% modulus in the longitudinal and transverse directions measured for each test piece, calculate the 5% modulus per unit area based on the following formula, and round off to the third decimal place.
‧每單位面積重量的5%模數((N/25mm)/(g/m2))=[5%模數的平均值(N/25mm)]/單位面積重量(g/m2)。 ‧5% modulus of weight per unit area ((N/25mm)/(g/m 2 ))=[average value of 5% modulus (N/25mm)]/weight per unit area (g/m 2 ).
接著,對於製造本發明之紡黏不織布之方法的較佳態樣具體地說明。 Next, a preferred aspect of the method for producing the spunbond nonwoven fabric of the present invention will be specifically described.
本發明之紡黏不織布係藉由紡黏法所製造的長纖維不織布。不織布之製造方法沒有特別的限制,例 如可舉出紡黏法、閃式紡絲法(flash spinning method)、濕式法、梳理法(card method)及氣流成網法(air-laid method)等。特別地,紡黏法除了生產性、機械強度優異之外,亦可抑制在短纖維不織布所容易引起的起毛、纖維的脫落。又,藉由將所捕集的紡黏不織纖維網或經熱壓接的紡黏不織布(皆標記為S)以SS、SSS及SSSS進行複數層積層,而生產性、質地均勻性提升,因此為較佳的態樣。 The spunbond nonwoven fabric of the present invention is a long fiber nonwoven fabric produced by the spunbond method. The method for producing the nonwoven fabric is not particularly limited, and examples thereof include a spunbond method, a flash spinning method, a wet method, a card method, an air-laid method, and the like. . In particular, in addition to being excellent in productivity and mechanical strength, the spunbond method can also suppress fuzzing and fiber shedding that are easily caused in short-fiber nonwoven fabrics. In addition, by laminating the captured spunbond nonwoven web or thermocompression bonded spunbond nonwoven fabric (all marked as S) with SS, SSS and SSSS, the productivity and texture uniformity are improved, Therefore, it is a better form.
於紡黏法中,首先從紡絲嘴,將熔融的熱塑性樹脂作為長纖維紡出,將其藉由噴射器,以壓縮空氣進行吸引延伸後,在移動的網狀物上捕集纖維而得到不織纖維網。進一步對於所得之不織纖維網施予熱接著處理,而得到紡黏不織布。 In the spunbond method, the molten thermoplastic resin is first spun out from the spinning nozzle as long fibers, and after being sucked and stretched by an ejector with compressed air, the fibers are collected on a moving mesh. Nonwoven web. Further, heat-bonding treatment is applied to the obtained nonwoven fiber web to obtain a spunbond nonwoven fabric.
紡絲嘴或噴射器之形狀沒有特別的限制,例如可採用圓形或矩形等各種形狀者。其中,從壓縮空氣的使用量比較少而能量成本優異,不易引起紗線彼此的熔接、摩擦,紗線的開纖亦容易來看,較佳使用矩形紡嘴與矩形噴射器之組合。 The shape of the spinneret or the injector is not particularly limited, and various shapes such as a circle or a rectangle can be used, for example. Among them, the use of compressed air is relatively small, the energy cost is excellent, the yarns are not easily welded and rubbed together, and the yarns are easy to open, and a combination of a rectangular spinning nozzle and a rectangular jet is preferred.
於本發明中,將聚烯烴系樹脂在擠壓機中熔融、計量,供給至紡絲嘴,作為長纖維紡出。將聚烯烴系樹脂熔融、紡絲時的紡絲溫度較佳為200~270℃,更佳為210~260℃,進一步較佳為220~250℃。藉由將紡絲溫度設為上述範圍內,可作成安定的熔融狀態,得到優異的紡絲安定性。 In the present invention, the polyolefin-based resin is melted and measured in an extruder, supplied to a spinning nozzle, and spun out as a long fiber. The spinning temperature at the time of melting and spinning the polyolefin resin is preferably 200 to 270°C, more preferably 210 to 260°C, and further preferably 220 to 250°C. By setting the spinning temperature within the above-mentioned range, a stable molten state can be obtained, and excellent spinning stability can be obtained.
紡絲嘴之背壓較佳設為0.1~6.0MPa。藉由 將背壓較佳設為0.1~6.0MPa,更佳設為0.3~6.0MPa,進一步較佳設為0.5~6.0MPa,可防止:吐出均勻性變差而發生纖維直徑偏差,或者因提高耐壓性而紡嘴大型化。紡絲嘴之背壓可藉由紡嘴的吐出孔徑或吐出孔深度、紡絲溫度等而調整,其中吐出孔徑之貢獻大。 The back pressure of the spinning nozzle is preferably set to 0.1-6.0 MPa. By making the back pressure preferably 0.1 to 6.0 MPa, more preferably 0.3 to 6.0 MPa, and still more preferably 0.5 to 6.0 MPa, it is possible to prevent the occurrence of fiber diameter deviation due to deterioration of discharge uniformity, or to increase the Pressure resistance and larger size of the spinning nozzle. The back pressure of the spinneret can be adjusted by the discharge aperture or depth of the spinneret, and the spinning temperature, among which the contribution of the discharge aperture is large.
所紡出的長纖維之紗線隨後被冷卻。作為將所紡出的紗線予以冷卻之方法,例如可舉出將冷風強制地噴吹到紗線之方法、以紗線周圍的氣體環境溫度進行自然冷卻之方法、及調整紡絲嘴與噴射器間的距離之方法等,或者可採用組合此等方法之方法。又,冷卻條件可考慮紡絲嘴之每單孔的吐出量、紡絲溫度及氣體環境溫度等,適宜調整而採用。 The spun filament yarn is then cooled. As a method of cooling the spun yarn, for example, a method of forcibly blowing cold air to the yarn, a method of natural cooling at the ambient temperature of the yarn around the yarn, and adjustment of the spinning nozzle and jet The method of the distance between the devices, etc., or a method of combining these methods can be used. In addition, the cooling conditions can be appropriately adjusted and adopted in consideration of the discharge rate per single hole of the spinning nozzle, the spinning temperature, the gas ambient temperature, and the like.
接著,經冷卻固化的紗線係藉由從噴射器所噴射出的壓縮空氣來牽引及延伸。 Then, the cooled and solidified yarn is drawn and extended by compressed air ejected from the ejector.
紡絲速度較佳為3,500~6,500m/分鐘,更佳為4,000~6,500m/分鐘,進一步較佳為4,500~6,500m/分鐘。藉由將紡絲速度設為3,500~6,500m/分鐘,變得具有高生產性,而且纖維的配向結晶化係進行,可得到高強度的長纖維。通常若提高紡絲速度,則紡絲性變差而無法安定地生產紗線,但如前述,藉由使用具有特定範圍的MFR之聚烯烴系樹脂,可將所意圖的聚烯烴纖維安定地紡絲。 The spinning speed is preferably 3,500 to 6,500 m/min, more preferably 4,000 to 6,500 m/min, still more preferably 4,500 to 6,500 m/min. By setting the spinning speed to 3,500 to 6,500 m/min, high productivity is achieved, and the orientation and crystallization of the fibers are advanced, and high-strength long fibers can be obtained. Generally, if the spinning speed is increased, the spinnability deteriorates and the yarn cannot be stably produced. However, as described above, by using a polyolefin-based resin having an MFR in a specific range, the intended polyolefin fiber can be spun stably. Silk.
接著,將所得之長纖維捕集在移動的網狀物上而得到不織纖維網。 Next, the obtained long fibers are collected on a moving web to obtain a nonwoven web.
於本發明中,亦較佳的態樣為對於不織纖維 網,在網狀物上從其單面來抵接熱平坦輥而使其暫時接著。藉由成為如此,可在網狀物上搬運中,防止不織纖維網的表層捲起或者飄動而質地變差,改善從補集紗線到熱壓接為止的搬運性。 In the present invention, it is also preferable that the nonwoven web is temporarily attached to the web by abutting the hot flat roll from one side thereof. By doing so, it is possible to prevent the surface layer of the nonwoven web from curling or fluttering during conveyance on the web and to prevent the texture from deteriorating, and to improve the conveyability from the yarn replenishment to the thermocompression bonding.
接著,藉由將所得之不織纖維網熱接著,可得到所意圖的紡黏不織布。 Next, by thermally bonding the obtained nonwoven web, the intended spunbond nonwoven fabric can be obtained.
將不織纖維網進行熱接著之方法沒有特別的限制,例如可舉出藉由上下一對的在輥表面上分別施有雕刻(凹凸部)的熱壓花輥、包含一個輥表面為平坦(平滑)的輥與另一個在輥表面上施有雕刻(凹凸部)的輥之組合的熱壓花輥、及包含上下一對的平坦(平滑)輥之組合的熱壓延輥等各種輥而進行熱接著之方法,或藉由喇叭(horn)的超音波振動而使其熱熔接之超音波接著等之方法。 The method for thermally bonding the nonwoven web is not particularly limited. For example, a pair of upper and lower thermal embossing rolls having engravings (concavities and convexities) on the roll surface, including one roll with a flat surface ( Various types of rolls, such as a combination of a smooth) roll and another roll with engraving (concave and convex) on the surface of the roll, and a combination of a pair of upper and lower flat (smooth) rolls and a hot calender roll. A method of performing thermal bonding, or a method of ultrasonic bonding in which heat is welded by ultrasonic vibration of a horn.
其中,從生產性優異,能以部分的熱接著部賦予強度,且在非接著部保持不織布才有的手感、肌膚觸感來看,較佳的態樣為使用上下一對的在輥表面分別施有彫刻(凹凸部)的熱壓花輥、或包含一個輥表面為平坦(平滑)的輥與另一個在輥表面上施有雕刻(凹凸部)的輥之組合的熱壓花輥。 Among them, from the viewpoint of being excellent in productivity, being able to impart strength to a part of the thermally bonded part, and to maintain the hand and skin feel of a non-woven fabric in the non-bonded part, it is preferable to use a pair of upper and lower pairs on the surface of the roll, respectively. A thermal embossing roll to which engravings (concavities and convexities) are applied, or a thermal embossing roll comprising a combination of a roll having a flat (smooth) roll surface and another roll having engravings (concavities and convexities) applied to the roll surface.
作為熱壓花輥之表面材質,為了得到充分的熱壓接效果,且防止一方的壓花輥之彫刻(凹凸部)轉印到另一方的輥表面,較佳的態樣為使金屬製輥與金屬製輥成對。 As the surface material of the thermal embossing roll, in order to obtain a sufficient thermal pressure bonding effect and prevent the engraving (concave and convex portion) of one embossing roll from being transferred to the surface of the other roll, a metal roll is preferably used. Pairs with metal rollers.
利用如此的熱壓花輥之壓花接著面積率較佳 為5~30%。藉由將接著面積較佳設為5%以上,更佳設為8%以上,進一步較佳設為10%以上,作為紡黏不織布,可得到能供實用的強度。另一方面,藉由將接著面積較佳設為30%以下,更佳設為25%以下,進一步較佳設為20%以下,作為衛生材料用的紡黏不織布,可得到尤其適合於紙尿布用途使用之適度的柔軟性。即使於使用超音波接著時,接著面積率較佳亦為同樣之範圍。 The area ratio of embossing using such a hot embossing roll is preferably 5 to 30%. By making the bonding area preferably 5% or more, more preferably 8% or more, and further preferably 10% or more, practical strength can be obtained as a spunbond nonwoven fabric. On the other hand, by making the bonding area preferably 30% or less, more preferably 25% or less, and still more preferably 20% or less, it is possible to obtain a spunbond nonwoven fabric for sanitary materials, which is particularly suitable for disposable diapers. Moderate softness for use. Even when ultrasonic bonding is used, the bonding area ratio is preferably within the same range.
此處所謂的接著面積,係指接著部在紡黏不織布整體中所占之比例。具體而言,當藉由一對具有凹凸的輥進行熱接著時,係指上側輥的凸部與下側輥的凸部重疊而抵接於不織纖維網的部分(接著部)在紡黏不織布整體中所占之比例。又,當藉由具有凹凸的輥與平坦輥進行熱接著時,係指具有凹凸的輥之凸部抵接於不織纖維網的部分(接著部)在紡黏不織布整體中所占之比例。又,進行超音波接著時,係指藉由超音波加工所熱熔接的部分(接著部)在紡黏不織布整體中所占之比例。 The so-called bonding area here refers to the proportion of the bonding portion in the entire spunbond nonwoven fabric. Specifically, when thermal bonding is performed by a pair of rolls having concavo-convex, it means that the portion (bonded portion) where the convex portion of the upper roll and the convex portion of the lower roll overlap and abut against the nonwoven web is spunbonded. The proportion of non-woven fabric as a whole. In addition, when thermal bonding is performed by a roll having unevenness and a flat roll, it refers to the proportion of the portion (bonding portion) where the convex portion of the roll having unevenness abuts on the nonwoven web in the entire spunbond nonwoven fabric. In addition, when ultrasonic bonding is performed, it refers to the proportion of the portion (bonded portion) thermally welded by ultrasonic processing in the entire spunbond nonwoven fabric.
因熱壓花輥或超音波接著所造成的接著部之形狀沒有特別的限定,例如可使用圓形、橢圓形、正方形、長方形、平行四邊形、菱形、正六角形及正八角形等。又,接著部較佳為在紡黏不織布之長度方向(搬運方向)與寬度方向上各自以一定的間隔均勻地存在。藉由成為如此,可減低紡黏不織布之強度偏差。 The shape of the bonding portion formed by hot embossing rolls or ultrasonic bonding is not particularly limited, for example, circle, ellipse, square, rectangle, parallelogram, rhombus, regular hexagon and regular octagon can be used. Moreover, it is preferable that the adhesive portion is uniformly present at predetermined intervals in each of the longitudinal direction (conveying direction) and the width direction of the spunbonded nonwoven fabric. By doing so, the variation in strength of the spunbond nonwoven fabric can be reduced.
熱接著時的熱壓花輥之表面溫度,設為相對於所使用的聚烯烴系樹脂之熔點而言為-50~-15℃者係較佳的態樣。藉由相對於聚烯烴系樹脂之熔點而將熱輥 之表面溫度較佳設為-50℃以上者,更佳設為-45℃以上者,可使其適度地熱接著,得到能供實用的強度之紡黏不織布。又,藉由相對於聚烯烴系樹脂之熔點而將熱壓花輥之表面溫度較佳設為-15℃以下者,更佳設為-20℃以下者,而抑制過度的熱接著,作為衛生材料用之紡黏不織布,可得到尤其適合於紙尿布用途使用之適度的柔軟性。 The surface temperature of the heat embossing roll at the time of thermal bonding is preferably -50 to -15° C. with respect to the melting point of the polyolefin-based resin used. By setting the surface temperature of the heat roller to preferably -50°C or higher, more preferably -45°C or higher with respect to the melting point of the polyolefin resin, it is possible to moderately thermally bond and obtain practical strength. of spunbond nonwovens. Moreover, by setting the surface temperature of the thermal embossing roll to preferably -15°C or lower, more preferably -20°C or lower with respect to the melting point of the polyolefin-based resin, excessive thermal bonding can be suppressed, and as a hygienic The spunbond non-woven fabric used as the material can obtain moderate softness especially suitable for the use of disposable diapers.
熱接著時之熱壓花輥的線壓較佳為50~500N/cm。藉由將輥的線壓較佳設為50N/cm以上,更佳設為100N/cm以上,進一步較佳設為150N/cm以上,可使其適度地熱接著,得到能供實用的強度之紡黏不織布。另一方面,藉由將熱壓花輥的線壓較佳設為500N/cm以下,更佳設為400N/cm以下,進一步較佳設為300N/cm以下,作為衛生材料用之紡黏不織布,可得到尤其適合於紙尿布用途使用之適度的柔軟性。 The linear pressure of the hot embossing roll during thermal bonding is preferably 50 to 500 N/cm. By setting the linear pressure of the roller to be preferably 50 N/cm or more, more preferably 100 N/cm or more, and still more preferably 150 N/cm or more, it is possible to moderately thermally bond, and to obtain a spinning of practical strength. Sticky nonwoven. On the other hand, by setting the linear pressure of the hot embossing roll to preferably 500 N/cm or less, more preferably 400 N/cm or less, and further preferably 300 N/cm or less, it is used as a spunbond nonwoven fabric for sanitary materials. , can obtain moderate softness especially suitable for the use of disposable diapers.
又,於本發明中,以調整紡黏不織布的厚度為目的,在利用上述的熱壓花輥的熱接著之前及/或之後,可藉由包含上下一對的平坦輥的熱壓延輥而施予熱壓接。所謂上下一對的平坦輥,係在輥之表面上無凹凸的金屬製輥或彈性輥,可使金屬製輥與金屬製輥成對,或者使金屬製輥與彈性輥成對而使用。 In addition, in the present invention, for the purpose of adjusting the thickness of the spunbond nonwoven fabric, before and/or after the thermal bonding with the above-mentioned thermal embossing rolls, a thermal calendering roll including a pair of upper and lower flat rolls can be used. Apply thermocompression. The upper and lower pair of flat rolls are metal rolls or elastic rolls with no unevenness on the surface of the rolls. Metal rolls and metal rolls can be used in pairs, or metal rolls and elastic rolls can be used in pairs.
又,此處所謂的彈性輥,係包含與金屬製輥相較更具有彈性的材質的輥。作為彈性輥,例如可舉出紙、棉及聚芳醯胺紙等之所謂的紙輥,或包含胺基甲酸酯(urethane)系樹脂、環氧系樹脂、矽系樹脂、聚酯系樹 脂及硬質橡膠、及此等之混合物的樹脂製輥等。 In addition, the elastic roll referred to here includes a roll made of a material more elastic than a metal roll. Examples of the elastic roll include so-called paper rolls such as paper, cotton, and polyaramide paper, and those containing urethane-based resins, epoxy-based resins, silicone-based resins, and polyester-based resins. And hard rubber, and resin rolls of these mixtures, etc.
接著,基於實施例而具體地說明本發明之紡黏不織布。另外,於各物性之測定中,沒有特別的記載者係基於前述方法進行測定。 Next, the spunbond nonwoven fabric of the present invention will be specifically described based on examples. In addition, in the measurement of each physical property, there is no specific description that the measurement is based on the aforementioned method.
(1)聚烯烴系樹脂之熔體流動速率(MFR)(g/10分鐘): (1) Melt flow rate (MFR) of polyolefin resin (g/10 minutes):
聚烯烴系樹脂之MFR係在荷重為2.16kg、溫度為230℃之條件下測定。 The MFR of the polyolefin resin was measured under the conditions of a load of 2.16 kg and a temperature of 230°C.
(2)紡絲速度(m/分鐘): (2) Spinning speed (m/min):
從上述之平均單纖維直徑與所使用的聚烯烴系樹脂之固體密度,將長度每10,000m的質量當作平均單纖維纖度(dtex),將小數點以下第二位予以四捨五入而算出。從平均單纖維纖度與以各條件設定的紡絲嘴單孔所吐出的樹脂之吐出量(以下,簡稱單孔吐出量)(g/分鐘),基於下式而算出紡絲速度。 From the above-mentioned average single fiber diameter and the solid density of the polyolefin-based resin used, the mass per 10,000 m of length was regarded as the average single fiber fineness (dtex), and the value was calculated by rounding off to the second decimal place. The spinning speed was calculated based on the following formula from the average single fiber fineness and the resin discharge rate (hereinafter referred to as single hole discharge rate) (g/min) from the spinning nozzle set under each condition.
‧紡絲速度(m/分鐘)=(10000×[單孔吐出量(g/分鐘)])/[平均單纖維纖度(dtex)]。 ‧Spinning speed (m/min)=(10000×[single hole output (g/min)])/[average single fiber fineness (dtex)].
(3)紡黏不織布之根據反射光亮度之纖維分散度: (3) Fiber dispersion of spunbond nonwovens according to reflected light brightness:
於紡黏不織布之根據反射光亮度之纖維分散度之測定中,於影像掃描使用彩色複合機「DocuCentre-VI C4471 PFS」(Fuji Xerox股份有限公司)。 In the measurement of the fiber dispersion degree according to the reflected light brightness of the spunbond nonwoven fabric, a color laminator "DocuCentre-VI C4471 PFS" (Fuji Xerox Co., Ltd.) was used for the image scanning.
(4)紡黏不織布之根據KES法之表面粗糙度SMD(μm): (4) Surface roughness SMD (μm) of spunbond non-woven fabric according to KES method:
於測定中,使用KATO TECH公司製自動化表面試驗機「KES-FB4-AUTO-A」。表面粗糙度SMD係在紡黏不織布之兩面進行測定,表1記載此等之中較小的值。 In the measurement, an automatic surface tester "KES-FB4-AUTO-A" manufactured by KATO TECH Co., Ltd. was used. The surface roughness SMD is measured on both sides of the spunbond nonwoven fabric, and Table 1 describes the smaller value among these.
(5)紡黏不織布之根據KES法之平均摩擦係數MIU、紡黏不織布之根據KES法之平均摩擦係數之變動MMD: (5) The average friction coefficient MIU of the spunbond non-woven fabric according to the KES method, and the change of the average friction coefficient of the spunbond non-woven fabric according to the KES method MMD:
於測定中,使用KATO TECH公司製自動化表面試驗機「KES-FB4-AUTO-A」。平均摩擦係數MIU係在紡黏不織布之兩面進行測定,表1記載此等之中較小的值。 In the measurement, an automatic surface tester "KES-FB4-AUTO-A" manufactured by KATO TECH Co., Ltd. was used. The average friction coefficient MIU is measured on both sides of the spunbond nonwoven fabric, and Table 1 describes the smaller value among these.
(6)紡黏不織布之熔體流動速率(MFR)(g/10分鐘): (6) Melt flow rate (MFR) of spunbond non-woven fabric (g/10min):
紡黏不織布之熔體流動速率係根據ASTM D1238,在荷重為2160g、溫度為230℃之條件下測定。 The melt flow rate of the spunbond nonwoven fabric was determined according to ASTM D1238 under the conditions of a load of 2160 g and a temperature of 230°C.
(7)紡黏不織布之手感 (7) The feel of spunbond nonwovens
採集尺寸100mm×100mm之樣品,官能檢查員(panelist)20人觸摸不織布,各自藉由以下的5等級之基準來評價紡黏不織布之手感。接著,合計各官能檢查員的判斷點數,當作紡黏不織布之手感,將80點以上當作合格。手感較佳為85點以上,更佳為90點以上。 A sample with a size of 100 mm×100 mm was collected, and 20 panellists touched the nonwoven fabric, and each evaluated the hand of the spunbond nonwoven fabric according to the following 5-level criteria. Next, the judgment points of each sensory inspector were totaled, and the spunbonded nonwoven fabric was regarded as the hand feeling, and 80 points or more were regarded as pass. The feel is preferably 85 points or more, more preferably 90 points or more.
5點:非常良好(感覺到緩衝性、柔軟性皆優異的舒適度) 5 points: very good (feeling of comfort with excellent cushioning and softness)
4點:良好(5點與3點之中間) 4 points: good (between 5 points and 3 points)
3點:普通(感覺到緩衝性、柔軟性) 3 points: Normal (feel cushioning, softness)
2點:差(3點與1點之中間) 2 points: difference (between 3 points and 1 point)
1點:非常差(感覺到缺少緩衝性、柔軟性之至少一 者) 1 point: very poor (at least one of cushioning and softness is felt to be lacking)
(實施例1) (Example 1)
將由熔體流動速率(MFR)為200g/10分鐘、熔點為163℃的均聚物所構成之聚丙烯樹脂在擠壓機中熔融,從孔徑為0.30mm、孔深度為2mm之矩形紡嘴,在紡絲溫度為235℃、單孔吐出量為0.32g/分鐘下紡出。將所紡出的紗線冷卻固化後,將其在矩形噴射器中,藉由將噴射器壓力設為0.35MPa的壓縮空氣而進行牽引、延伸,捕集在移動的網狀物上。藉此,形成由聚丙烯長纖維所構成之不織纖維網。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為10.1μm,由此所換算的紡絲速度為4,411m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。 A polypropylene resin composed of a homopolymer having a melt flow rate (MFR) of 200 g/10 minutes and a melting point of 163° C. was melted in an extruder, and the diameter of the A rectangular spinning nozzle with a hole depth of 0.30 mm and a hole depth of 2 mm was spun at a spinning temperature of 235°C and a single hole discharge rate of 0.32 g/min. After the spun yarn was cooled and solidified, it was drawn and stretched in a rectangular jet with compressed air whose jet pressure was 0.35 MPa, and was collected on a moving web. Thereby, a nonwoven web composed of polypropylene long fibers was formed. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 10.1 μm, and the spinning speed converted from this was 4,411 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good.
接著,將所形成的紡黏不織纖維網,使用由以下的上輥、下輥所構成之上下一對的熱壓花輥,於線壓:300N/cm、熱接著溫度:130℃的條件下熱接著,得到單位面積重量18g/m2之紡黏不織布。 Next, the formed spunbond nonwoven web was subjected to the following conditions of a pair of upper and lower thermal embossing rolls consisting of the following upper and lower rolls, under the conditions of linear pressure: 300 N/cm, and thermal bonding temperature: 130°C After heating, a spunbond nonwoven fabric with a weight per unit area of 18 g/m 2 was obtained.
(上輥):金屬製且施有水珠圖樣之雕刻的接著面積率16%之壓花輥 (Top roller): Embossing roller made of metal and engraved with a water drop pattern with an area ratio of 16%
(下輥):金屬製平坦輥 (Lower roll): Metal flat roll
表1中顯示對於所得之紡黏不織布評價的結果。 Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics.
(實施例2) (Example 2)
除了將由均聚物所構成之聚丙烯樹脂作成MFR為 155g/10分鐘、熔點為163℃者,將噴射器之壓力設為0.20MPa以外,藉由與實施例1相同之方法,得到紡黏不織布。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為11.8μm,由此所換算的紡絲速度為3,216m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。表1中顯示對於所得之紡黏不織布評價的結果。 A spunbond nonwoven fabric was obtained by the same method as in Example 1, except that the polypropylene resin composed of homopolymer was made into one with MFR of 155g/10min and melting point of 163°C, and the pressure of the ejector was set to 0.20MPa. . In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 11.8 μm, and the spinning speed converted from this was 3,216 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics.
(實施例3) (Example 3)
除了將由均聚物所構成之聚丙烯樹脂作成MFR為800g/10分鐘、熔點為163℃者以外,藉由與實施例1相同之方法,得到紡黏不織布。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為8.4μm,由此所換算的紡絲速度為6,422m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。表1中顯示對於所得之紡黏不織布評價的結果。 A spunbond nonwoven fabric was obtained by the same method as in Example 1, except that the polypropylene resin composed of the homopolymer was made into one having an MFR of 800 g/10 minutes and a melting point of 163°C. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 8.4 μm, and the spinning speed converted from this was 6,422 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics.
(實施例4) (Example 4)
除了將由均聚物所構成之聚丙烯樹脂作成MFR為800g/10分鐘、熔點為163℃者,將單孔吐出量設為0.21g/分鐘以外,藉由與實施例1相同之方法,得到紡黏不織布。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為7.2μm,由此所換算的紡絲速度為5,668m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。表1中顯示對於所得之紡黏不織布評價的 結果。 Spinning was obtained in the same manner as in Example 1, except that the polypropylene resin composed of a homopolymer had an MFR of 800 g/10 min, a melting point of 163° C., and a single-hole discharge rate of 0.21 g/min. Sticky nonwoven. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 7.2 μm, and the spinning speed converted from this was 5,668 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. Table 1 shows the results of evaluation for the obtained spunbond nonwoven fabric.
(實施例5) (Example 5)
除了將由均聚物所構成之聚丙烯樹脂作成MFR為155g/10分鐘者,將噴射器之壓力設為0.38MPa以外,藉由與實施例1相同之方法,得到紡黏不織布。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為10.1μm,由此所換算的紡絲速度為4,393m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。表1中顯示對於所得之紡黏不織布評價的結果。 A spunbond nonwoven fabric was obtained by the same method as in Example 1, except that the polypropylene resin composed of the homopolymer had an MFR of 155 g/10 minutes and the pressure of the ejector was set to 0.38 MPa. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 10.1 μm, and the spinning speed converted from this was 4,393 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics.
(實施例6) (Example 6)
除了使用在由均聚物所構成之聚丙烯樹脂中添加有1.0質量%的伸乙基雙硬脂酸醯胺作為脂肪酸醯胺化合物者以外,藉由與實施例1相同之方法,得到紡黏不織布。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為10.1μm,由此所換算的紡絲速度為4,352m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。表1中顯示對於所得之紡黏不織布評價的結果。 A spunbond was obtained in the same manner as in Example 1, except that 1.0% by mass of ethylidene bisstearate amide was used as the fatty acid amide compound in the polypropylene resin composed of the homopolymer Not woven. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 10.1 μm, and the spinning speed converted from this was 4,352 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics.
(比較例1) (Comparative Example 1)
除了將由均聚物所構成之聚丙烯樹脂作成MFR為60g/10分鐘、熔點為163℃者,將單孔吐出量設為0.43g/分鐘,將噴射器之壓力設為0.15MPa以外,藉由與實施 例1相同之方法,得到紡黏不織布。構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為14.0μm,由此所換算的紡絲速度為3,070m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。另外,於相同條件下將噴射器壓力設為0.35MPa時,斷線頻繁發生,無法紡絲。表1中顯示對於所得之紡黏不織布評價的結果。所得之紡黏不織布係平均單纖維直徑與纖維分散度大,因此表面粗糙度SMD亦大。 Except that the polypropylene resin composed of the homopolymer was made into a MFR of 60 g/10 min and a melting point of 163° C., the discharge rate per hole was set to 0.43 g/min, and the pressure of the ejector was set to 0.15 MPa. In the same manner as in Example 1, a spunbond nonwoven fabric was obtained. The characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 14.0 μm, and the spinning speed converted from this was 3,070 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. In addition, when the ejector pressure was set to 0.35 MPa under the same conditions, thread breakage frequently occurred, and spinning was not possible. Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics. The obtained spunbond nonwoven has large average single fiber diameter and fiber dispersion, so the surface roughness SMD is also large.
(比較例2) (Comparative Example 2)
除了將單孔吐出量設為0.43g/分鐘,將噴射器之壓力設為0.30MPa以外,藉由與實施例1相同之方法,得到紡黏不織布。構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為12.9μm,由此所換算的紡絲速度為3,617m/分鐘。關於紡絲性,在1小時的紡絲中未看見斷線而為良好。表1中顯示對於所得之紡黏不織布評價的結果。所得之紡黏不織布雖然纖維分散度小,但是平均單纖維直徑大,因此表面粗糙度SMD亦大。 A spunbonded nonwoven fabric was obtained by the same method as in Example 1, except that the discharge rate per hole was set to 0.43 g/min and the pressure of the ejector was set to 0.30 MPa. The characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 12.9 μm, and the spinning speed converted from this was 3,617 m/min. With regard to spinnability, no thread breakage was observed during 1 hour of spinning, and it was good. Table 1 shows the results of the evaluation of the obtained spunbond nonwoven fabrics. Although the obtained spunbond nonwoven fabric has a small fiber dispersion, the average single fiber diameter is large, so the surface roughness SMD is also large.
(比較例3) (Comparative Example 3)
參考日本國特開2013-159884號公報之實施例1,嘗試得到本案發明之紡黏不織布。將熔體流動速率(MFR)為35g/10分鐘的聚丙烯樹脂在擠壓機中熔融,從孔徑為0.35mm、孔深度為7mm之矩形紡嘴,在紡絲溫度為255℃、單孔吐出量為0.56g/分鐘下紡出。將所紡出的紗 線冷卻固化後,將其在矩形噴射器中,藉由將噴射器壓力設為0.35MPa的壓縮空氣而進行牽引、延伸,捕集在移動的網狀物上。藉此,形成由聚丙烯長纖維所構成之不織纖維網。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為12.5μm,由此所換算的紡絲速度為5,015m/分鐘。關於紡絲性,在1小時的紡絲中斷線頻繁發生而為不良。 Referring to Example 1 of Japanese Patent Application Laid-Open No. 2013-159884, an attempt was made to obtain the spunbond nonwoven fabric of the present invention. A polypropylene resin with a melt flow rate (MFR) of 35 g/10 minutes was melted in an extruder, from the hole diameter A rectangular spinning nozzle with a hole depth of 0.35 mm and a hole depth of 7 mm was spun at a spinning temperature of 255°C and a single hole discharge rate of 0.56 g/min. After the spun yarn was cooled and solidified, it was drawn and stretched in a rectangular jet with compressed air whose jet pressure was 0.35 MPa, and was collected on a moving web. Thereby, a nonwoven web composed of polypropylene long fibers was formed. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 12.5 μm, and the spinning speed converted from this was 5,015 m/min. With regard to spinnability, yarn breakage occurred frequently within 1 hour of spinning, and it was unfavorable.
接著,將所形成的紡黏不織纖維網,使用由以下的上輥、下輥所構成之上下一對的熱壓花輥,於線壓:300N/cm、熱接著溫度:130℃的條件下熱接著,得到單位面積重量17g/m2之紡黏不織布。 Next, the formed spunbond nonwoven web was subjected to the following conditions of a pair of upper and lower thermal embossing rolls consisting of the following upper and lower rolls, under the conditions of linear pressure: 300 N/cm, and thermal bonding temperature: 130°C After heating, a spunbond nonwoven fabric with a weight per unit area of 17 g/m 2 was obtained.
(上輥):金屬製且施有水珠圖樣之雕刻的接著面積率6%之壓花輥 (Top roller): Embossing roller made of metal and engraved with a water drop pattern with an area ratio of 6%
(下輥):金屬製平坦輥 (Lower roll): Metal flat roll
對於所得之紡黏不織布,選擇斷線沒有混入的部分進行評價。表1中顯示結果。所得之紡黏不織布係平均單纖維直徑與纖維分散度大,因此表面粗糙度SMD亦大。 About the obtained spunbond nonwoven fabric, the part which did not mix|blend a broken thread was selected and evaluated. The results are shown in Table 1. The obtained spunbond nonwoven has large average single fiber diameter and fiber dispersion, so the surface roughness SMD is also large.
(比較例4) (Comparative Example 4)
參考日本國特開平8-3853號公報之實施例5,嘗試得到本案發明之紡黏不織布。將熔體流動速率(MFR)為70g/10分鐘的聚丙烯樹脂在擠壓機中熔融,從孔徑為0.60mm、孔深度為1.2mm之矩形紡嘴,在紡絲溫度為245℃、單孔吐出量為0.35g/分鐘下紡出。將所紡出的紗 線冷卻固化後,將其在密閉型的矩形噴射器中,藉由將噴射器壓力設為0.35MPa的壓縮空氣而進行牽引、延伸,捕集在移動的網狀物上。藉此,形成由聚丙烯長纖維所構成之不織纖維網。另外,構成所形成的紡黏不織纖維網之纖維的特性,係平均單纖維直徑為8.4μm,由此所換算的紡絲速度為6,980m/分鐘。關於紡絲性,在1小時的紡絲中斷線頻繁發生而為不良。 Referring to Example 5 of Japanese Patent Application Laid-Open No. 8-3853, an attempt was made to obtain the spunbond nonwoven fabric of the present invention. A polypropylene resin with a melt flow rate (MFR) of 70 g/10 min was melted in an extruder, from the hole diameter A rectangular spinning nozzle with a diameter of 0.60 mm and a hole depth of 1.2 mm was spun at a spinning temperature of 245° C. and a single hole discharge rate of 0.35 g/min. After cooling and solidifying the spun yarn, it is drawn and stretched in a closed rectangular ejector with compressed air with an ejector pressure of 0.35 MPa, and collected on a moving web . Thereby, a nonwoven web composed of polypropylene long fibers was formed. In addition, the characteristics of the fibers constituting the formed spunbond nonwoven web were that the average single fiber diameter was 8.4 μm, and the spinning speed converted from this was 6,980 m/min. With regard to spinnability, yarn breakage occurred frequently within 1 hour of spinning, and it was unfavorable.
接著,將所形成的紡黏不織纖維網,使用由以下的上輥、下輥所構成之上下一對的熱壓花輥,於線壓:300N/cm、熱接著溫度:130℃的條件下熱接著,得到單位面積重量17g/m2之紡黏不織布。 Next, the formed spunbond nonwoven web was subjected to the following conditions of a pair of upper and lower thermal embossing rolls consisting of the following upper and lower rolls, under the conditions of linear pressure: 300 N/cm, and thermal bonding temperature: 130°C After heating, a spunbond nonwoven fabric with a weight per unit area of 17 g/m 2 was obtained.
(上輥):金屬製且施有水珠圖樣之雕刻的接著面積率21%之壓花輥 (Upper roll): Embossing roll made of metal and engraved with a water drop pattern with an area ratio of 21%
(下輥):金屬製平坦輥 (Lower roll): Metal flat roll
對於所得之紡黏不織布,選擇斷線沒有混入的部分進行評價。表1中顯示結果。所得之紡黏不織布雖然平均單纖維直徑小,但是纖維分散度大,因此表面粗糙度SMD亦大。 About the obtained spunbond nonwoven fabric, the part which did not mix|blend a broken thread was selected and evaluated. The results are shown in Table 1. Although the average single fiber diameter of the obtained spunbond nonwoven fabric is small, the fiber dispersion is large, so the surface roughness SMD is also large.
實施例1~6之平均單纖維直徑為6.5~11.9μm,根據反射光亮度之纖維分散度為10以下,且根據KES法之表面粗糙度SMD為1.0~2.6μm的實施例1~6之紡黏不織布,係質地均勻,表面光滑且手感、肌膚觸感優異,更具有高柔軟性。又,平均單纖維直徑變得愈細,有平均摩擦係數愈增加之傾向,但是添加有伸乙基雙硬脂酸醯胺的實施例6之紡黏不織布,係平均摩擦係數被減低,乾爽感、柔軟性增加,特別適合作為衛生材料用途。 The average single fiber diameter of Examples 1 to 6 is 6.5 to 11.9 μm, the fiber dispersion according to the reflected light brightness is 10 or less, and the surface roughness SMD of the KES method is 1.0 to 2.6 μm. Spinning of Examples 1 to 6 Sticky non-woven fabric with uniform texture, smooth surface, excellent hand and skin feel, and high softness. In addition, as the average single fiber diameter becomes smaller, the average friction coefficient tends to increase, but the spunbond nonwoven fabric of Example 6 to which ethylene bisstearate is added has a lower average friction coefficient and a dry feeling. , Increased flexibility, especially suitable for use as sanitary materials.
另一方面,比較例1與比較例3中所示之平均單纖維直徑與纖維分散度大且根據KES法之表面粗糙度SMD大之紡黏不織布、比較例2中所示之平均單纖維直徑大且根據KES法之表面粗糙度SMD大之紡黏不織布、及比較例4中所示的根據反射光亮度之纖維分散度大且根據KES法之表面粗糙度SMD大之紡黏不織布,相較於本發明之不織布係粗糙感大,手感、肌膚觸感差。又,比較例3與比較例4中所示的使用MFR比較小的聚丙烯樹脂之紡黏不織布,係於高紡絲速度下之紡絲性差,無法安定地生產。 On the other hand, spunbond nonwoven fabrics with large average single fiber diameter and fiber dispersion degree shown in Comparative Example 1 and Comparative Example 3 and large surface roughness SMD according to the KES method, and the average single fiber diameter shown in Comparative Example 2 The spunbond nonwoven fabric with large surface roughness SMD according to the KES method, and the spunbond nonwoven fabric with large fiber dispersion according to the reflected light brightness and large surface roughness SMD according to the KES method shown in Comparative Example 4, compared In the non-woven fabric of the present invention, the roughness is large, and the hand and skin feel are poor. In addition, the spunbond nonwoven fabrics using polypropylene resin having a relatively small MFR shown in Comparative Example 3 and Comparative Example 4 had poor spinnability at high spinning speeds and could not be stably produced.
雖然已使用特定的態樣詳細地說明本發明,但是在不脫離本發明的意圖與範圍下,各式各樣的變更及變形係可能的,此對於本業者而言可明知。另外,本申請案係以2018年2月28日申請的日本發明專利申請案(特願2018-034867)及2018年7月27日申請的日本發明專利申請案(特願2018-141046)為基礎,其整體係藉由 引用而被援用。 Although the present invention has been described in detail using specific aspects, it is clear for those skilled in the art that various changes and modifications are possible without departing from the intent and scope of the present invention. In addition, this application is based on the Japanese Patent Application for Invention (Japanese Patent Application No. 2018-034867) filed on February 28, 2018 and the Japanese Patent Application for Invention (Japanese Patent Application No. 2018-141046) filed on July 27, 2018 , the entirety of which is cited by reference.
本發明之紡黏不織布由於生產性高,質地均勻,表面光滑且手感、肌膚觸感優異,更具有高柔軟性,故可適合利用於拋棄式紙尿布或衛生棉等之衛生材料用途。於衛生材料之中,尤其適合利用於紙尿布之背片。 The spunbond nonwoven fabric of the present invention has high productivity, uniform texture, smooth surface, excellent hand and skin feel, and high softness, so it can be suitably used for sanitary materials such as disposable diapers or sanitary napkins. Among sanitary materials, it is especially suitable for the back sheet of paper diapers.
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| JP7676819B2 (en) * | 2020-03-31 | 2025-05-15 | 東レ株式会社 | Spunbond nonwoven fabric |
| WO2021215492A1 (en) * | 2020-04-22 | 2021-10-28 | 花王株式会社 | Non-woven fabric for hygiene, hygienic product and absorbent article provided with same, and method for manufacturing non-woven fabric for hygiene |
| WO2022113711A1 (en) * | 2020-11-27 | 2022-06-02 | 東レ株式会社 | Spunbond nonwoven fabric, and hygienic material equipped therewith |
| CN113355755A (en) * | 2020-12-15 | 2021-09-07 | 浙江青昀新材料科技有限公司 | Polymer sheet prepared by flash evaporation method |
| TW202321037A (en) * | 2021-08-06 | 2023-06-01 | 日商花王股份有限公司 | Nonwoven fabric for hygiene and method for producing same |
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| CN114657701B (en) * | 2022-03-28 | 2023-04-18 | 厦门当盛新材料有限公司 | Microwave heat seal flash spinning non-woven fabric process method, microwave heat seal device and non-woven fabric preparation equipment |
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