JP2006291404A - Moisture absorbing nonwoven fabric - Google Patents
Moisture absorbing nonwoven fabric Download PDFInfo
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- JP2006291404A JP2006291404A JP2005115208A JP2005115208A JP2006291404A JP 2006291404 A JP2006291404 A JP 2006291404A JP 2005115208 A JP2005115208 A JP 2005115208A JP 2005115208 A JP2005115208 A JP 2005115208A JP 2006291404 A JP2006291404 A JP 2006291404A
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- nonwoven fabric
- hygroscopic
- sheet
- heat
- web layer
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- 239000004745 nonwoven fabric Substances 0.000 title claims abstract description 76
- 239000000835 fiber Substances 0.000 claims abstract description 106
- 239000000843 powder Substances 0.000 claims abstract description 52
- 238000000034 method Methods 0.000 claims abstract description 45
- 239000000853 adhesive Substances 0.000 claims abstract description 35
- 239000000463 material Substances 0.000 claims abstract description 27
- 229920000098 polyolefin Polymers 0.000 claims abstract description 25
- 230000001070 adhesive effect Effects 0.000 claims abstract description 13
- 239000002585 base Substances 0.000 claims description 32
- -1 alkali metal salts Chemical class 0.000 claims description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 14
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 5
- 239000000758 substrate Substances 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 239000005909 Kieselgur Substances 0.000 claims description 3
- 235000017166 Bambusa arundinacea Nutrition 0.000 claims description 2
- 235000017491 Bambusa tulda Nutrition 0.000 claims description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 claims description 2
- 229920002845 Poly(methacrylic acid) Polymers 0.000 claims description 2
- 229910021536 Zeolite Inorganic materials 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 239000011425 bamboo Substances 0.000 claims description 2
- 239000003610 charcoal Substances 0.000 claims description 2
- 239000002274 desiccant Substances 0.000 claims description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical group O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- 239000002808 molecular sieve Substances 0.000 claims description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- 241001330002 Bambuseae Species 0.000 claims 1
- 238000007669 thermal treatment Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 58
- 238000002844 melting Methods 0.000 description 27
- 230000008018 melting Effects 0.000 description 22
- 239000004698 Polyethylene Substances 0.000 description 17
- 239000000306 component Substances 0.000 description 17
- 239000002131 composite material Substances 0.000 description 15
- 239000004743 Polypropylene Substances 0.000 description 14
- 230000035699 permeability Effects 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000032798 delamination Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000004566 building material Substances 0.000 description 3
- 238000003490 calendering Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000008358 core component Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000007731 hot pressing Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 101100087414 Arabidopsis thaliana RH20 gene Proteins 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- 101000813777 Homo sapiens Splicing factor ESS-2 homolog Proteins 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 102100039575 Splicing factor ESS-2 homolog Human genes 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000003230 hygroscopic agent Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- BWHLPLXXIDYSNW-UHFFFAOYSA-N ketorolac tromethamine Chemical compound OCC(N)(CO)CO.OC(=O)C1CCN2C1=CC=C2C(=O)C1=CC=CC=C1 BWHLPLXXIDYSNW-UHFFFAOYSA-N 0.000 description 1
- 239000012567 medical material Substances 0.000 description 1
- 239000004750 melt-blown nonwoven Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 238000009512 pharmaceutical packaging Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000001393 triammonium citrate Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
本発明は、高い吸湿性を有する不織布に関する。本発明の吸湿性不織布は、湿度調節や結露防止の機能を有する上に、吸湿性粉体の脱落がなく、柔軟性にも富むので各種の建築材料、衛生材料、生活用材料、医薬・食品用部材、電機電子部品、電線材料などの広い範囲の用途に適用できる。 The present invention relates to a nonwoven fabric having high hygroscopicity. The hygroscopic nonwoven fabric of the present invention has functions of humidity control and dew condensation prevention, and does not fall off hygroscopic powder, and is also flexible, so various building materials, sanitary materials, daily life materials, pharmaceuticals and foods It can be applied to a wide range of applications such as industrial members, electrical and electronic parts, and wire materials.
従来より、不織布は、土木資材や衛生資材などに広く用いられており、不織布と無機充填材とを組み合わせた不織布複合体が提案されている。
例えば、特許文献1(特開昭62−104956号公報)には、合成パルプ、天然パルプと、シリカ、アルミナ、ケイソウ土などの無機充填剤との乾式抄造(Air Lay)からなるシートが示されている。しかしながら、この用途は、自動車内装材などの熱プレス成型に用いるシートに係わるものであって、本発明が意図する吸湿性シートとは全く異なる用途であり、また、本発明の目的である吸湿性シートにとって重要な構成要件である、表裏層を形成する不織布の複合についても全く言及も示唆もない。
Conventionally, nonwoven fabrics have been widely used in civil engineering materials and sanitary materials, and nonwoven fabric composites combining nonwoven fabrics and inorganic fillers have been proposed.
For example, Patent Document 1 (Japanese Patent Laid-Open No. 62-104956) discloses a sheet made of dry paper making (Air Lay) of synthetic pulp, natural pulp, and inorganic fillers such as silica, alumina, diatomaceous earth and the like. ing. However, this application relates to a sheet used for hot press molding of automobile interior materials and the like, and is completely different from the hygroscopic sheet intended by the present invention, and is also a hygroscopic property that is the object of the present invention. There is no mention or suggestion about the composite of the nonwoven fabric forming the front and back layers, which is an important component for the sheet.
また、特許文献2(特開2003−113580号公報)には、吸湿性微粒子と短繊維を混合した状態でネットに気流で吹き付けてウェブ化する高吸湿性不織布複合体を得る方法が示されており、無機微粒子を繊維に固着するため、不織布に熱融着繊維を含有させたり、片面または両面に繊維シートなどの保護層を設けることもできる、との記載がある。同特許文献の実施例2には、目付60g/m2、厚み0.3mmのポリエステルスパンボンド不織布上に、多孔質シリカ微粒子と熱融着性の芯鞘ポリエステル短繊維とを混合して気流にて吹き付け積層し、熱プレスした例が開示されている。しかしながら、不織布を構成する繊維径の平均値は、好ましくは0.1〜1,000μmとあるのみで、本発明の重要な構成要件である、多分岐繊維構造の合成パルプを粉体と混合することによって粉体の脱落防止や、粉体の均一な分散を改良する技術については、なんら触れられていない。 Patent Document 2 (Japanese Patent Application Laid-Open No. 2003-113580) discloses a method for obtaining a highly hygroscopic nonwoven fabric composite that is webbed by blowing air current on a net in a state where hygroscopic fine particles and short fibers are mixed. In order to fix the inorganic fine particles to the fiber, there is a description that the non-woven fabric can contain a heat-sealing fiber, or a protective layer such as a fiber sheet can be provided on one side or both sides. In Example 2 of the patent document, porous silica fine particles and heat-fusible core-sheath polyester short fibers are mixed on a polyester spunbonded nonwoven fabric having a basis weight of 60 g / m 2 and a thickness of 0.3 mm to produce an air current. An example of spraying, laminating and hot pressing is disclosed. However, the average value of the fiber diameter constituting the nonwoven fabric is preferably only 0.1 to 1,000 μm, and the synthetic pulp having a multi-branched fiber structure, which is an important constituent element of the present invention, is mixed with the powder. There is no mention of a technique for preventing the powder from falling off and improving the uniform dispersion of the powder.
さらに、特許文献3(特開2003−340231号公報)に記載された発明は、吸湿性粉体と極細短繊維との混合物を、多孔性支持体上に噴出させて、吸湿性シートを形成するものであり、片面または両面に不織布を積層することも開示されている。そして、特許文献3には、上記極細短繊維が絡んだ状態にあると、圧縮気体の作用によっても、極細短繊維を個々の極細短繊維に解繊し、均一に分散させるのが困難になるとの記載があり(同特許文献の段落「0047」)、吸湿性粉体とフラッシュ紡糸法により得られた多分岐繊維構造のポリオレフィン系合成パルプとを組合わせることにより、粉体脱落が少なく、柔軟性に富み、各種の用途に応用することが可能な吸湿性シートが得られるという本発明の技術思想とは合い入れない考え方が示されている。 Furthermore, the invention described in Patent Document 3 (Japanese Patent Laid-Open No. 2003-340231) forms a hygroscopic sheet by ejecting a mixture of hygroscopic powder and ultrafine short fibers onto a porous support. It is also disclosed that a non-woven fabric is laminated on one side or both sides. And in patent document 3, when it is in the state in which the said ultra-fine short fiber was entangled, it will become difficult to disperse | distribute an ultra-fine short fiber to each ultra-fine short fiber by the effect | action of compressed gas, and to disperse | distribute uniformly (Paragraph “0047” of the same patent document), combining a hygroscopic powder and a polyolefin-based synthetic pulp having a multi-branch fiber structure obtained by the flash spinning method, reduces the amount of powder falling off and is flexible. A concept that is not compatible with the technical idea of the present invention that a hygroscopic sheet that is rich in properties and can be applied to various uses is shown.
本発明は、ポリオレフィン系合成パルプと吸湿性粉体とを組合わせ、エアレイド法を用いることにより、粉体脱落が少なく、柔軟性に富み、各種の用途に応用することが可能な吸湿性シートを提供することを目的とする。 The present invention provides a hygroscopic sheet that combines a polyolefin synthetic pulp and a hygroscopic powder and uses the airlaid method to reduce powder fall-off, have high flexibility, and can be applied to various applications. The purpose is to provide.
本発明は、繊度が1〜4dtexの熱接着性繊維を60重量%以上含み、熱処理により繊維間結合された目付が10〜100g/m2の不織布からなる基材シート上に、ポリオレフィン系合成パルプと吸湿性粉体とが90/10〜10/90重量%の比率で混合された成分からなり、目付が20〜1,500g/m2のウェブ層をエアレイド法により形成し、積層一体化させてなる吸湿性不織布に関する。
本発明では、ポリオレフィン系合成パルプと吸湿性粉体とからなるウェブ層の上に、さらに、繊度が1〜4dtexの熱接着性繊維を60重量%以上含み、熱処理により繊維間結合された目付が10〜100g/m2の不織布からなる上層シートを積層してもよい。
また、上記基材シートとウェブ層との間および/またはウェブ層と上層シートとの間に、さらに熱接着性複合繊維からなる不織布を介在させてもよい。
本発明の吸湿性不織布は、熱処理されていることが好ましい。
The present invention provides a polyolefin-based synthetic pulp on a base sheet made of a nonwoven fabric containing 60% by weight or more of heat-adhesive fibers having a fineness of 1 to 4 dtex and having a basis weight of 10 to 100 g / m 2 bonded between fibers by heat treatment. And a hygroscopic powder are mixed in a ratio of 90/10 to 10/90% by weight, and a web layer having a basis weight of 20 to 1,500 g / m 2 is formed by the airlaid method and laminated and integrated. This relates to a hygroscopic nonwoven fabric.
In the present invention, on the web layer composed of the polyolefin synthetic pulp and the hygroscopic powder, the basis weight further includes 60% by weight or more of heat-adhesive fibers having a fineness of 1 to 4 dtex and are bonded between fibers by heat treatment. You may laminate | stack the upper layer sheet | seat which consists of 10-100 g / m < 2 > nonwoven fabric.
Moreover, you may interpose the nonwoven fabric which consists of thermoadhesive conjugate fiber further between the said base material sheet and a web layer, and / or between a web layer and an upper layer sheet.
The hygroscopic nonwoven fabric of the present invention is preferably heat treated.
本発明では、ポリオレフィン系合成パルプと吸湿性粉体とからウェブを形成させるに際し、エアレイド法を採用しているので、気流中でポリオレフィン系合成パルプと吸湿性粉体とが絡み合って、オレフィン系合成パルプ中に吸湿性粉体が絡合して、形成されるウェブからの吸湿性粉体の脱落が少なく、また、あらかじめ基材シート(キャリアシート)を用い、この上にエアレイド法により、オレフィン系合成パルプと吸湿性粉体とからなるウェブを積層させるので、仮に吸湿性粉体が生成ウェブから脱落しても、この基材シートに捕集されて、系外に脱落することもない。また、得られる吸湿性不織布は、柔軟性に富み、吸湿性に優れる。
また、上層を積層させた吸湿性不織布は、表裏ともに、吸湿性粉体の脱落がない。
さらに、基材シート層とウェブ層および/またはウェブ層と上層との間に、さらに熱接着性複合繊維からなる不織布を介在させると、得られる吸湿性不織布の層間剥離や吸湿性粉体の脱落をさらに抑制することができる。
また、本発明の吸湿性不織布は、熱風処理あるいは熱ロールによるカレンダー加工などの熱処理により、さらに層間剥離や吸湿性粉体の脱落を抑えることができる。
In the present invention, when the web is formed from the polyolefin synthetic pulp and the hygroscopic powder, the airlaid method is employed, so that the polyolefin synthetic pulp and the hygroscopic powder are entangled in the air stream, Hygroscopic powder is entangled in the pulp, so that the hygroscopic powder does not fall off from the formed web. In addition, a base sheet (carrier sheet) is used in advance, and an olefin type is formed thereon by the airlaid method. Since webs made of synthetic pulp and hygroscopic powder are laminated, even if the hygroscopic powder falls off the generated web, it is not collected by this base sheet and dropped out of the system. Moreover, the hygroscopic nonwoven fabric obtained is rich in flexibility and excellent in hygroscopicity.
Moreover, the hygroscopic nonwoven fabric laminated with the upper layer does not drop the hygroscopic powder on both the front and back sides.
Furthermore, when a non-woven fabric made of a heat-adhesive conjugate fiber is further interposed between the base sheet layer and the web layer and / or the web layer and the upper layer, delamination of the resulting hygroscopic non-woven fabric and removal of the hygroscopic powder Can be further suppressed.
In addition, the hygroscopic nonwoven fabric of the present invention can further suppress delamination and hygroscopic powder dropping by heat treatment such as hot air treatment or calendering with a hot roll.
基材シート:
本発明に用いられる基材シートは、繊度が1〜4dtexの熱接着性繊維を60重量%以上含み、熱処理により繊維間結合された、目付が10〜100g/m2の不織布から構成される。なお、この基材シートは、あらかじめ熱処理により繊維間結合されていなくてもよく、例えば、本発明の吸湿性不織布製造工程の最終段階で、上記ウェブ層や上層シートとともに熱処理されて繊維間結合されたものであってもよい。
この基材シートは、カード法、スパンボンド法、メルトブロー法、エアレイド法、または湿式抄造法のいずれで作成されたものでもよいが、好ましくはエアレイド法である。
Base sheet:
The base sheet used in the present invention is composed of a non-woven fabric having a basis weight of 10 to 100 g / m 2 containing 60% by weight or more of heat-adhesive fibers having a fineness of 1 to 4 dtex and bonded between fibers by heat treatment. The base sheet may not be bonded between fibers by heat treatment in advance. For example, in the final stage of the hygroscopic nonwoven fabric manufacturing process of the present invention, the base sheet is heat treated together with the web layer or the upper layer sheet and bonded between fibers. It may be.
The base sheet may be prepared by any of the card method, the spun bond method, the melt blow method, the air laid method, or the wet papermaking method, but is preferably the air laid method.
基材シートに用いられる熱接着性繊維としては、熱接着性複合繊維が好適である。例えば、低融点成分を鞘成分とし、高融点成分を芯成分とする芯鞘型、一方が低融点、他方が高融点成分であるサイドバイサイド型などが挙げられる。これらの複合繊維の両方の成分の組み合わせとしては、PP〔ポリプロピレン〕/PE(ポリエチレン)、PET(ポリエチレンテレフタレート)/PE、PP/低融点共重合PP、PET/低融点共重合ポリエステルなどが挙げられる。ここで、上記低融点共重合ポリエステルの例としては、ポリエチレンテレフタレート、ポリプロピレンテレフタレート、ポリブチレンテレフタレートなどを基本骨格として、イソフタル酸、5−金属スルホイソフタル酸などの芳香族ジカルボン酸、アジピン酸、セバチン酸などの脂肪族ジカルボン酸、ジエチレングリコール、プロピレングリコール、1,4−ブタンジオールなどの脂肪族多価アルコールなどとの変性共重合などが挙げられる。 As the heat-adhesive fiber used for the base sheet, a heat-adhesive conjugate fiber is suitable. For example, a core-sheath type in which a low melting point component is a sheath component and a high melting point component is a core component, a side-by-side type in which one is a low melting point and the other is a high melting point component. Examples of the combination of both components of these composite fibers include PP [polypropylene] / PE (polyethylene), PET (polyethylene terephthalate) / PE, PP / low-melting copolymer PP, PET / low-melting copolymer polyester, and the like. . Here, examples of the low-melting point copolyester include polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, etc. as a basic skeleton, aromatic dicarboxylic acids such as isophthalic acid and 5-metal sulfoisophthalic acid, adipic acid, and sebacic acid. And a modified copolymer with an aliphatic polycarboxylic acid such as diethylene glycol, diethylene glycol, propylene glycol, 1,4-butanediol and the like.
低融点成分である熱接着成分の融点は、通常、110〜160℃、好ましくは120〜155℃である。110℃未満の場合、不織布としての耐熱性が低いので実用性に欠ける。一方、160℃を超えると、不織布製造工程における熱処理温度を高くする必要が生じ、生産性が落ち、実用的でないばかりか、後述するエアレイド繊維層との熱圧一体化における接着効果も期待できなくなる。 The melting point of the thermal adhesive component, which is a low melting point component, is usually 110 to 160 ° C., preferably 120 to 155 ° C. When the temperature is less than 110 ° C., the heat resistance of the nonwoven fabric is low, so that it is not practical. On the other hand, when the temperature exceeds 160 ° C., it is necessary to increase the heat treatment temperature in the nonwoven fabric production process, the productivity is lowered, and it is not practical, and the adhesive effect in the hot-pressure integration with the airlaid fiber layer described later cannot be expected. .
熱接着性繊維の繊度は、1〜4dtex、好ましくは1.1〜3dtexである。1dtex未満の場合は、細い繊維どうしが絡まり易くなり、他の繊維との混合も難しくなって、地合いの不均一性や塊状欠点発生のリスクが大になる。一方、4dtexを超えた太い繊維の場合は、同一混合率でも繊維本数がダウンする結果となるので、吸湿性粉体脱落防止、強度付与、ヒートシール性付与などの効果が薄れる。
なお、基材シートの製法がエアレイド法の場合は、熱接着性繊維は、繊維長が2〜15mmであることが好ましく、さらに好ましくは3〜10mmである。繊維長が2mm未満の場合は、強度アップなどの効果が十分で無く、一方、15mmを超えると、繊維どうしが絡まり易くなり、工程性や地合いの悪化につながりやすい。
The fineness of the heat-adhesive fiber is 1 to 4 dtex, preferably 1.1 to 3 dtex. If it is less than 1 dtex, thin fibers tend to be entangled with each other and mixing with other fibers becomes difficult, increasing the risk of uneven texture and occurrence of bulk defects. On the other hand, in the case of a thick fiber exceeding 4 dtex, the number of fibers decreases even at the same mixing rate, and thus the effects of preventing hygroscopic powder from falling off, imparting strength, and imparting heat sealability are reduced.
In addition, when the manufacturing method of a base material sheet is an airlaid method, it is preferable that the fiber length is 2-15 mm, More preferably, it is 3-10 mm. When the fiber length is less than 2 mm, the effect of increasing the strength is not sufficient. On the other hand, when the fiber length exceeds 15 mm, the fibers tend to be entangled with each other, leading to deterioration in processability and texture.
なお、熱接着性繊維は捲縮していても、していなくてもよく、またストランドチョップであってもよい。捲縮している場合、ジグザグ型の二次元捲縮繊維およびスパイラル型やオーム型などの三次元(立体)捲縮繊維の何れも使用できる。 The heat-adhesive fiber may be crimped or not, and may be a strand chop. When crimped, both zigzag-type two-dimensional crimped fibers and spiral-type and ohmic-type three-dimensional (three-dimensional) crimped fibers can be used.
また、これらの熱接着性繊維以外の繊維としては、例えばPP繊維、PET繊維、PBT繊維、ナイロン6繊維、ナイロン6,6繊維、芳香族ポリアミド繊維、アクリル繊維、合成パルプ(例えば、三井化学(株)製SWPのような、PEやPPを素材とする多分岐フィブリル状繊維)、木材パルプ、麻、レーヨン、ビスコース繊維などを本発明の趣旨、効果を阻害しない範囲で混合しておいても良い。この場合、他の繊維の比率は50重量%未満に留めるのが好ましい。50重量%以上であると、不織布強力やヒートシール性に影響が出るばかりか、熱接着性のない繊維は実使用中に脱落し易くなる。 Examples of fibers other than these heat-adhesive fibers include PP fibers, PET fibers, PBT fibers, nylon 6 fibers, nylon 6,6 fibers, aromatic polyamide fibers, acrylic fibers, synthetic pulp (for example, Mitsui Chemicals ( Multi-branched fibrillar fibers made of PE or PP, such as SWP manufactured by Co., Ltd.), wood pulp, hemp, rayon, viscose fibers, etc. are mixed within a range not impairing the gist and effect of the present invention. Also good. In this case, the proportion of other fibers is preferably kept below 50% by weight. If it is 50% by weight or more, not only the strength of the nonwoven fabric and the heat sealability will be affected, but fibers without thermal adhesiveness will easily fall off during actual use.
基材シートの目付は、10〜100g/m2、好ましくは12〜80g/m2である。10g/m2未満の場合は、ウェブ層に存在する吸湿性粉体が基材シートで捕捉されずに脱落したり、不織布強力も低くなるので実使用で破壊などのトラブルを引き起こし易い。一方、100g/m2を超えると、エアレイド法の基材として必要な通気度2秒以下の要件を確保できなくなる傾向が生じるばかりか、低通気性であるがために本発明の意図する吸湿性に悪影響が出る。
なお、基材シートの通気度は、2秒以下であることが好ましい。エアレイド法は、通気性材料の上部から繊維と空気の混合体を噴出させ、下部からサクションで空気を引きつつ、通気性材料上に繊維層を形成する方法なので、基材となる基材シートの通気度は重要な要件となる。2秒を超えた通気性の悪い場合は、エアレイド繊維層が不均一になり易く、且つ生産性も悪化する。通気度は、好ましくは0.5〜2秒である。
The basis weight of the base sheet is 10 to 100 g / m 2 , preferably 12 to 80 g / m 2 . When the amount is less than 10 g / m 2, the hygroscopic powder present in the web layer falls off without being captured by the base sheet, and the strength of the nonwoven fabric is lowered, so troubles such as breakage are likely to occur during actual use. On the other hand, if it exceeds 100 g / m 2 , not only will the requirement of air permeability of 2 seconds or less necessary as a base material for the airlaid method be apt to occur, but the moisture absorption intended by the present invention is due to low air permeability. Adversely affected.
The air permeability of the base sheet is preferably 2 seconds or less. The airlaid method is a method in which a fiber layer is formed on a breathable material by ejecting a mixture of fibers and air from the top of the breathable material and drawing air from the bottom by suction. Air permeability is an important requirement. When the air permeability exceeding 2 seconds is poor, the air-laid fiber layer is likely to be non-uniform and the productivity is also deteriorated. The air permeability is preferably 0.5 to 2 seconds.
なお、基材シートは、ウェブ層との積層に際し、同時に作成してもよいが、例えば、あらかじめエアレイド法で作製、熱処理された基材シートを用いることがエアレイド法による製造工程を簡略化できる点で好ましい。 The base sheet may be formed at the same time as the lamination with the web layer. For example, the use of a base sheet that has been prepared and heat-treated in advance by the airlaid method can simplify the manufacturing process by the airlaid method. Is preferable.
エアレイド不織布製造法によるウェブ層の形成と積層一体化:
次に、上記基材シートの上にエアレイド法で、ポリオレフィン系合成パルプと吸湿性粉体からなるウェブ層を形成する。すなわち、多孔質ネットコンベアー上に位置する単台または多数台の噴き出し部から、ポリオレフィン系合成パルプと吸湿性粉体との混合物を噴出し、ネットコンベアー下面に配置した空気サクション部で吸引しながらネットコンベアー上にウェブ層を形成するものである。このとき、ネットコンベア上に上記基材である基材シートをあらかじめ敷いて置くことにより、一挙に積層体が得られる。その後、積層体に熱風処理、および/または熱圧カレンダー処理を加えてエアレイド層の繊維間結合、および基材との熱接着を形成して不織布シートとして一体化させる。
さらに、ウェブ層には、熱接着性繊維を併せて混合しておいても良い。この場合、粉体の固定・脱落防止、層間剥離強力の向上、などの効果が期待できる。ウェブ層に熱接着性繊維を併用すると、特に本発明のシートの端面からの粉体脱落防止には効果が大きい。熱接着性繊維としては、上記した熱接着性複合繊維が特に好適である。混合率は、ウェブ層全体の60重量%以下であることが好ましい。60重量%を超えると、熱処理後のシートの柔軟性が失われてくるばかりか、吸湿性粉体の周囲を多くの熱接着性繊維で覆う状態となり、吸湿性に悪影響を及ぼす。
繊維量、噴き出し条件、空気サクション条件、熱処理条件などを調節することにより必要な特性をコントロールすることができる。
Formation and lamination integration of web layer by airlaid nonwoven manufacturing method:
Next, a web layer made of polyolefin synthetic pulp and hygroscopic powder is formed on the base sheet by the airlaid method. That is, a mixture of polyolefin synthetic pulp and hygroscopic powder is ejected from a single unit or a large number of ejection units located on a porous net conveyor and sucked by an air suction unit arranged on the lower surface of the net conveyor. A web layer is formed on a conveyor. At this time, a laminated body can be obtained at once by placing a base material sheet as the base material on a net conveyor in advance. Thereafter, hot air treatment and / or hot-pressure calender treatment is applied to the laminate to form an airlaid layer-to-fiber bond and a thermal bond with the substrate to be integrated as a nonwoven sheet.
Furthermore, you may mix the heat bondable fiber together with the web layer. In this case, it is possible to expect effects such as fixing of powder, prevention of dropping, and improvement of delamination strength. When a heat-adhesive fiber is used in combination with the web layer, it is particularly effective for preventing powder from falling off from the end face of the sheet of the present invention. As the heat-adhesive fiber, the above-mentioned heat-adhesive conjugate fiber is particularly suitable. The mixing ratio is preferably 60% by weight or less of the entire web layer. When it exceeds 60% by weight, not only the flexibility of the sheet after heat treatment is lost, but also the surroundings of the hygroscopic powder are covered with many heat-adhesive fibers, which adversely affects the hygroscopicity.
Necessary characteristics can be controlled by adjusting the fiber amount, ejection conditions, air suction conditions, heat treatment conditions, and the like.
ここで、ポリオレフィン系合成パルプは、例えば、高温、高圧状態にあるポリオレフィン、水の沸点よりも低い沸点を有する脂肪酸炭化水素および脂環族炭化水素から選ばれるポリマー用溶媒、および水よりなる分散液であって、減圧領域中に急速に放出したときに、実質的にすべての溶媒が蒸発し、かつ水の実質的蒸発を起こさない温度にある分散液を、沈殿ノズルを通して減圧領域中に放出して、ポリオレフィンを水中に分散した繊維状物質として回収し、この水中に分散した繊維状物質を、直ちに、50℃以上の初期温度にある状態で、界面活性剤の叩解またはリファイニングすることによって得られる。このポリオレフィン系合成パルプの製造方法は、例えば、特公昭52−47049号公報の第1欄の特許請求の範囲、第3欄第5行〜第19欄第25行に詳述されているが、本発明の趣旨、すなわち吸湿性粉体の捕捉作用を有するフィブリル状繊維からなるポリオレフィン系合成パルプの製法であれば、必ずしもこれらにこだわるものでは無い。
ポリオレフィン系合成パルプは、平均繊維長が0.5〜3mm、平均繊維径が1〜100μmのものが好適に使用できる。
また、このポリオレフィン系合成パルプの市販品としては、三井化学(株)製のSWP E790,E400,EST−8,E620,UL410,NL490,AU690,Y600,ESS−5,ESS−2,E380,E780,E90,UL415などが挙げられる。
Here, the polyolefin synthetic pulp is, for example, a high temperature, high pressure state polyolefin, a polymer solvent selected from a fatty acid hydrocarbon and an alicyclic hydrocarbon having a boiling point lower than the boiling point of water, and a dispersion comprising water. A dispersion at a temperature at which substantially all of the solvent evaporates and does not cause substantial evaporation of water when rapidly released into the vacuum zone, is released through the precipitation nozzle into the vacuum zone. The polyolefin is recovered as a fibrous material dispersed in water, and the fibrous material dispersed in water is obtained by beating or refining the surfactant immediately at an initial temperature of 50 ° C. or higher. It is done. The method for producing the polyolefin-based synthetic pulp is described in detail in, for example, the claims in the first column of JP-B-52-47049, column 3, line 5 to column 19, line 25. The gist of the present invention, that is, a method for producing a polyolefin-based synthetic pulp composed of fibrillar fibers having a trapping action for hygroscopic powder, is not necessarily limited to these.
As the polyolefin synthetic pulp, those having an average fiber length of 0.5 to 3 mm and an average fiber diameter of 1 to 100 μm can be suitably used.
Moreover, as a commercial item of this polyolefin synthetic pulp, SWP E790, E400, EST-8, E620, UL410, NL490, AU690, Y600, ESS-5, ESS-2, E380, E780 manufactured by Mitsui Chemicals, Inc. , E90, UL415, and the like.
これらのポリオレフィン系合成パルプは、多分岐繊維構造(フィブリル化して、多分岐、高比表面積を有する)なので、吸湿性粉体の捕捉性に優れる特徴を有する。また、エアレイド法により上記基材シートに吹き付けると、気流中でポリオレフィン系合成パルプと吸湿性粉体とが一体となったウェブ層が、該シート上に均一に載置されることになる。 Since these polyolefin-based synthetic pulps have a multi-branched fiber structure (fibrillated, multi-branched and have a high specific surface area), they have a feature of excellent hygroscopic powder capturing properties. Further, when the substrate sheet is sprayed by the airlaid method, the web layer in which the polyolefin synthetic pulp and the hygroscopic powder are integrated in an air current is uniformly placed on the sheet.
一方、ウェブ層を形成する他方の吸湿性粉体としては、吸湿性を有する粉体であればいかなるものでもよいが、好ましくはゼオライト、シリカ系粒子、アルミナゲル、アルミナ系粒子、シリカアルミナ系乾燥剤、けい藻土、木炭、竹炭、活性炭、モレキュラシーブス、ポリ(メタ)アクリル酸もしくはポリビニルピロリドンまたはこれらのアルカリ金属塩、などである。
これらの吸湿性粉体の平均粒径は、通常、0.01〜2mm、好ましくは0.1〜1mmである。
On the other hand, the other hygroscopic powder forming the web layer may be any hygroscopic powder, preferably zeolite, silica-based particles, alumina gel, alumina-based particles, silica-alumina-based dry Agents, diatomaceous earth, charcoal, bamboo charcoal, activated carbon, molecular sieves, poly (meth) acrylic acid or polyvinylpyrrolidone, or alkali metal salts thereof.
The average particle diameter of these hygroscopic powders is usually 0.01 to 2 mm, preferably 0.1 to 1 mm.
ウェブ層を形成するポリオレフィン系合成パルプと吸湿性粉体との混合比は、90/10〜10/90重量%、好ましくは80/20〜20/80重量%、さらに好ましくは70/30〜20/80重量%である。ポリオレフィン系合成パルプが10重量%未満では、吸湿性粉体の捕捉機能が充分でなくなり、粉体脱落しやすくなる。一方、吸湿性粉体が10重量%未満では、得られる吸湿性不織布の吸湿性が乏しく、本発明の意図するものでなくなる。 The mixing ratio of the polyolefin-based synthetic pulp forming the web layer and the hygroscopic powder is 90/10 to 10/90% by weight, preferably 80/20 to 20/80% by weight, and more preferably 70/30 to 20%. / 80% by weight. When the polyolefin-based synthetic pulp is less than 10% by weight, the function of capturing the hygroscopic powder is not sufficient, and the powder easily falls off. On the other hand, if the hygroscopic powder is less than 10% by weight, the hygroscopic nonwoven fabric obtained has poor hygroscopicity, which is not intended by the present invention.
なお、エアレイド法で形成するウェブ層は、通常、目付が20〜1,500g/m2、好ましくは40〜1,000g/m2である。20g/m2未満の場合、吸湿性、不織布強力、ヒートシール強力が低くなり、実用に適さない。一方、1,500g/m2を超えると、厚過ぎて柔軟性が乏しくなり、またエアレイド法で均一なウェブを形成するのが困難となり好ましくない。
本発明のウェブ層を作製するエアレイド法は、カード法などの既存の乾式不織布製造法に較べて、空気流によって容易に単繊維に解繊され易い、長さの短い繊維が使用できるので、極めて地合いの良好な、つまり均一性の良好な不織布が得られるという大きな特徴を有する。吸湿性の用途において、粉体漏れが少なく、かつ吸湿性が良いという性能に、均一性は重要な要件であり、既存のカード法不織布、スパンボンド不織布、メルトブロー不織布では得られ難い。また、本製造法によれば、タテ/ヨコの強力比率がほぼ1/1に近いというメリットも有する。
The web layer formed by the airlaid method usually has a basis weight of 20 to 1,500 g / m 2 , preferably 40 to 1,000 g / m 2 . When it is less than 20 g / m 2 , the hygroscopic property, the nonwoven fabric strength, and the heat seal strength are low, which is not suitable for practical use. On the other hand, if it exceeds 1,500 g / m 2 , it is not preferable because it is too thick and the flexibility becomes poor, and it becomes difficult to form a uniform web by the airlaid method.
The airlaid method for producing the web layer of the present invention is extremely easy to use because of the short length of fibers that can be easily defibrated to a single fiber by air flow, compared to existing dry nonwoven fabric manufacturing methods such as the card method. A great feature is that a non-woven fabric having good texture, that is, good uniformity can be obtained. In hygroscopic applications, uniformity is an important requirement for the performance of low powder leakage and good hygroscopicity, and is difficult to obtain with existing card method nonwoven fabrics, spunbond nonwoven fabrics, and melt blown nonwoven fabrics. Moreover, according to this manufacturing method, there is also a merit that the vertical / horizontal strength ratio is close to 1/1.
上層シート:
本発明の吸湿性不織布は、上記ウェブ層に存在する吸湿性粉体の脱落を一層防止し、また表面耐磨耗性などの機能を強化するために、このポリオレフィン系合成パルプと吸湿性粉体とからなるウェブ層の上に、さらに、繊度が1〜4dtexの熱接着性繊維を60重量%以上含み、熱処理により繊維間結合された目付が10〜100g/m2の不織布からなる上層シートを積層することが好ましい。
この上層シートとしては、上記基材シートと同様のものを挙げることができる。
Upper sheet:
The hygroscopic non-woven fabric of the present invention is made of this polyolefin synthetic pulp and hygroscopic powder in order to further prevent the hygroscopic powder present in the web layer from falling off and to enhance functions such as surface abrasion resistance. An upper sheet made of a non-woven fabric further comprising 60% by weight or more of heat-adhesive fibers having a fineness of 1 to 4 dtex and having a basis weight of 10 to 100 g / m 2 bonded between fibers by heat treatment. It is preferable to laminate.
Examples of the upper layer sheet include the same sheet as the base sheet.
熱接着性複合繊維からなる接着性不織布:
本発明の吸湿性不織布は、基シートとウェブ層との間、あるいは、ウェブ層と上層シートとの間の接合を確かなものとするために、これらの層間に、熱接着性複合繊維からなる接着性不織布を介在させることが好ましい。
接着性不織布を介在させるには、基材である上記基材シート上、および/または、ウェブ層の上に、エアレイド法で接着性不織布層を形成する。すなわち、多孔質ネットコンベアー上に位置する単台または多数台の噴き出し部から、接着成分の融点が110〜160℃の熱接着性複合繊維を空気流と共に噴出し、ネットコンベアー下面に配置した空気サクション部で吸引しながらネットコンベアー上に繊維層を形成するものである。このとき、ネットコンベア上に上記基材シート層、あるいは、基材シート層およびウェブ層をあらかじめ敷いて置くことにより、一挙に積層体が得られる。その後、積層体に熱風処理、および熱圧カレンダー処理を加えてエアレイド層の繊維間結合、および基材シート層との熱接着を形成して不織布シートとして一体化させる。
繊維量、噴き出し条件、空気サクション条件、熱処理条件などを調節することにより必要な特性をコントロールすることができる。
Adhesive nonwoven fabric made of heat-adhesive conjugate fiber:
The hygroscopic nonwoven fabric of the present invention comprises a heat-adhesive conjugate fiber between the base sheet and the web layer or between the web layer and the upper layer sheet in order to ensure the bonding. It is preferable to interpose an adhesive nonwoven fabric.
In order to interpose the adhesive nonwoven fabric, the adhesive nonwoven fabric layer is formed by the airlaid method on the substrate sheet as the substrate and / or the web layer. That is, an air suction unit in which a heat-adhesive conjugate fiber having a melting point of 110 to 160 ° C. of an adhesive component is ejected together with an air flow from a single unit or a plurality of ejection units located on a porous net conveyor, and arranged on the lower surface of the net conveyor. The fiber layer is formed on the net conveyor while sucking at the part. At this time, the base material sheet layer, or the base material sheet layer and the web layer are laid in advance on the net conveyor to obtain a laminated body at once. Thereafter, hot air treatment and hot-pressure calender treatment are applied to the laminate to form an airlaid layer-to-fiber bond and a thermal bond with the base sheet layer to be integrated as a nonwoven sheet.
Necessary characteristics can be controlled by adjusting the fiber amount, ejection conditions, air suction conditions, heat treatment conditions, and the like.
接着性不織布に用いられる熱接着性複合繊維としては、基材シートに用いられる熱接着性複合繊維と同様のものが用いられる。
接着性不織布の目付は、通常、2〜50g/m2、好ましくは4〜30g/m2であり、2g/m2未満では、基材シートとウェブ層、あるいは、ウェブ層と上層シートとの接着が不充分となる。一方、50g/m2を超えると厚すぎて吸湿性能に悪い影響を及ぼし易い。
As the heat-adhesive conjugate fiber used for the adhesive nonwoven fabric, those similar to the heat-adhesive conjugate fiber used for the base sheet are used.
Basis weight of the adhesive nonwoven fabric, usually, 2 to 50 g / m 2, preferably 4~30g / m 2, is less than 2 g / m 2, the base sheet and the web layer, or the web layer and the upper layer sheet Adhesion is insufficient. On the other hand, if it exceeds 50 g / m 2 , it is too thick and tends to adversely affect the hygroscopic performance.
熱処理:
本発明の吸湿性不織布は、以上のようにして得られる不織布積層体を熱処理することが好ましい。熱処理としては、熱風処理および/または熱圧処理が挙げられる。
このうち、繊維間結合を形成するための熱風処理としては、熱接着性複合繊維の低融点成分の融点以上の温度が必要である。しかしながら、低融点成分の融点よりも30℃以上高い場合、あるいは高融点成分(芯鞘型複合繊維の芯成分、あるいはサイドバイサイド型複合繊維の高融点成分)の融点以上の場合は、繊維の熱収縮が大きくなり易く、地合いの悪化を招いたり、はなはだしい場合は繊維の劣化を生じるので好ましくない。
熱風処理温度は、通常、110〜190℃、好ましくは120〜175℃である。
Heat treatment:
As for the hygroscopic nonwoven fabric of this invention, it is preferable to heat-process the nonwoven fabric laminated body obtained as mentioned above. Examples of the heat treatment include hot air treatment and / or hot pressure treatment.
Among these, the hot air treatment for forming the fiber-to-fiber bond requires a temperature equal to or higher than the melting point of the low-melting component of the heat-adhesive conjugate fiber. However, if the melting point is 30 ° C. or higher than the melting point of the low melting point component, or the melting point of the high melting point component (the core component of the core-sheath type composite fiber or the high melting point component of the side-by-side type composite fiber), the heat shrinkage of the fiber. Is liable to be large, which leads to deterioration of the texture, and in extreme cases, it causes deterioration of the fibers, which is not preferable.
The hot air treatment temperature is usually 110 to 190 ° C, preferably 120 to 175 ° C.
また、熱風処理したのち熱圧処理、具体的には熱圧カレンダー処理を加えても良い。カレンダー処理に用いるローラーとしては、全体に均一な熱圧を加えるため、平滑表面の一対の金属ローラー、または金属ローラーと弾性ローラーの組み合わせを用いることが好ましいが、多段ローラーであっても良い。また、本発明の趣旨を損なわない範囲であれば、凸凹表面のエンボスローラーであっても良い。 Further, after the hot air treatment, a hot pressure treatment, specifically, a hot pressure calendar treatment may be added. As a roller used for the calendering treatment, it is preferable to use a pair of metal rollers having a smooth surface or a combination of a metal roller and an elastic roller in order to apply a uniform heat pressure to the whole, but a multi-stage roller may also be used. In addition, an embossing roller with an uneven surface may be used as long as the gist of the present invention is not impaired.
カレンダー処理の場合、単に厚さ調整のためであれば常温(非加熱)〜高温度の任意の温度で加圧すれば良い。圧力は希望する厚さになるよう適宜選択することができる。熱圧カレンダーにより繊維間の熱結合を補強し、強度、表面耐摩耗性、層間剥離防止などを向上するためであれば、ローラー表面の温度は、熱接着性複合繊維の低融点成分の融点以上の温度が必要である。しかしながら、低融点成分の融点よりも30℃以上高い場合、あるいは高融点成分(芯鞘型複合繊維の芯成分、あるいはサイドバイサイド型複合繊維の高融点成分)の融点以上の場合は、繊維の熱収縮が大きくなり易いばかりか、ローラー表面への粘着が発生し、工程性に欠ける。融点未満の場合は、当然のことながら繊維間結合の補強が充分でなくなる。
繊維間結合を補強する場合の熱処理温度は、通常、110〜190℃、好ましくは120〜175℃である。
In the case of calendering, the pressure may be applied at any temperature from room temperature (non-heated) to high temperature if it is simply for thickness adjustment. The pressure can be appropriately selected to achieve a desired thickness. The temperature of the roller surface is higher than the melting point of the low-melting component of the heat-adhesive conjugate fiber so as to reinforce the thermal bond between the fibers with a hot-pressure calender and improve strength, surface abrasion resistance, delamination prevention, etc. Temperature is required. However, if the melting point is 30 ° C. or higher than the melting point of the low melting point component, or the melting point of the high melting point component (the core component of the core-sheath type composite fiber or the high melting point component of the side-by-side type composite fiber), the heat shrinkage of the fiber. Not only tends to be large, but also sticks to the roller surface and lacks processability. When the temperature is lower than the melting point, it is a matter of course that the reinforcement between the fibers is not sufficient.
The heat treatment temperature for reinforcing the fiber-to-fiber bond is usually 110 to 190 ° C, preferably 120 to 175 ° C.
また、カレンダー処理の線圧は、幅方向で均一な接圧になるよう設定すれば、任意の圧力を選択することができる。高圧の場合は密度・不織布強力・層間強力がアップし、厚さがダウンする。低圧の場合は勿論これに反する影響が出る。不織布強力を重視するのであれば極力高圧のほうが好ましい。柔軟性を重視するのであれば低圧の方が好ましい。カレンダー処理の線圧は、通常、10〜100kgf/cmの範囲で任意に選択できる。 Moreover, if the linear pressure of the calendar process is set so as to be a uniform contact pressure in the width direction, an arbitrary pressure can be selected. In the case of high pressure, the density, non-woven fabric strength and interlayer strength increase, and the thickness decreases. In the case of low pressure, of course, an adverse effect occurs. If importance is attached to the strength of the nonwoven fabric, a high pressure is preferred as much as possible. If flexibility is important, low pressure is preferable. The linear pressure of the calendar process can usually be arbitrarily selected in the range of 10 to 100 kgf / cm.
なお、得られる本発明の吸湿性不織布の厚さは、通常、0.3〜30mm、好ましくは0.5〜20mmであるが、ウェブ層の目付け(20〜1,500g/m2)に応じ、且つ用途に応じて設定することができる。
また、本発明の吸湿性不織布の総目付けは、通常、40〜1,800g/m2、好ましくは50〜1,500g/m2である。
In addition, although the thickness of the hygroscopic nonwoven fabric of this invention obtained is 0.3-30 mm normally, Preferably it is 0.5-20 mm, but according to the fabric weight (20-1,500 g / m < 2 >) of a web layer. And can be set according to the application.
The total weight of the hygroscopic nonwoven fabric of the present invention is usually 40 to 1,800 g / m 2 , preferably 50 to 1,500 g / m 2 .
以下、実施例を挙げ、本発明をさらに具体的に説明するが、本発明はこれらの実施例に限定されるものではない。 EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated further more concretely, this invention is not limited to these Examples.
実施例1
まず、PET(ポリエチレンテレフタレート)/PE(ポリエチレン)系複合繊維2.2dt×5mm(帝人ファイバー(株)、F6)を原料繊維として用い、エアレイド法によってシート化した。目付けは12g/m2に調整し、熱オーブン温度136℃で熱処理した。このシートの通気度は0.8秒であった。次に、このシートを基材シート(キャリアシート)として、その上にポリエチレン系合成パルプ(三井化学(株)、SWP・E795)20重量%と、粉砕B型シリカゲル(新越化成工業(株)、GB(W)30メッシュパス)80重量%との混合物を180g/m2となるようエアレイド法でウェブ層として形成した。さらに、この上部に、上記12g/m2のシートを上層シートとして載置して、これら複層シートを重ねたままで136℃の熱オーブンで熱風処理したのちに表面フラットな一対の金属ローラーで80℃、10kgf/cmで熱圧処理した。得られた目付け204g/m2の積層一体化不織布は、柔軟で粉漏れも無く、実用に耐える強度、耐表面摩耗性などを有し、吸湿性にも優れ、かつ一度吸湿させた後に低湿度の環境下で放湿する性質も示し、吸放湿性不織布として有用であった。
Example 1
First, a PET (polyethylene terephthalate) / PE (polyethylene) based composite fiber 2.2 dt × 5 mm (Teijin Fibers Ltd., F6) was used as a raw material fiber to form a sheet by an airlaid method. The basis weight was adjusted to 12 g / m 2 and heat-treated at a hot oven temperature of 136 ° C. The air permeability of this sheet was 0.8 seconds. Next, this sheet is used as a base sheet (carrier sheet), on which polyethylene synthetic pulp (Mitsui Chemicals Co., Ltd., SWP · E795) 20% by weight and crushed B-type silica gel (Shinetsu Chemical Industries Co., Ltd.) , GB (W) 30 mesh pass) was formed as a web layer by the airlaid method so as to be 180 g / m 2 . Further, the sheet of 12 g / m 2 is placed on the upper part as an upper layer sheet, and the multi-layer sheets are stacked and subjected to hot air treatment in a 136 ° C. hot oven, followed by a pair of metal rollers having a flat surface. Hot pressing was performed at 10 ° C. and 10 kgf / cm. The resulting laminated integrated nonwoven fabric with a basis weight of 204 g / m 2 is flexible and free of powder leakage, has practically strong strength, surface wear resistance, etc., has excellent hygroscopicity, and has low moisture after being absorbed once. It exhibited the property of releasing moisture under the environment, and was useful as a moisture absorbing / releasing nonwoven fabric.
比較例1
ウェブ層をすべてポリエチレン系合成パルプで構成し、その他は実施例1と同様にした。得られた積層一体化不織布は吸湿性に欠けるものであった。
Comparative Example 1
All web layers were made of polyethylene synthetic pulp, and the others were the same as in Example 1. The obtained laminated integrated nonwoven fabric lacked hygroscopicity.
比較例2
ウェブ層の組成中、ポリエチレン系合成パルプをPET/PE系複合繊維2.2dt×5mm(帝人ファイバー(株)、F6)に置き換えた以外は、すべて実施例1と同様にした。得られた積層一体化不織布は吸湿性を有するものの粉漏れが激しく、実用性に欠けるものであった。
Comparative Example 2
The same procedure as in Example 1 was conducted except that the polyethylene synthetic pulp was replaced with PET / PE composite fiber 2.2 dt × 5 mm (Teijin Fibers Ltd., F6) during the composition of the web layer. Although the obtained laminated integrated nonwoven fabric had hygroscopicity, powder leakage was severe and lacked practicality.
実施例2
まず、PP(ポリプロピレン)/PE系複合繊維2.2dt×51mm(チッソ(株)、ESC)を原料繊維として用い、カード法によって目付け16g/m2のウェブとし、136℃のエアスルータイプの熱オーブンで熱処理してシート化した。このシートの通気度は0.9秒であった。次に、このシートを基材シートとして、その上にポリエチレン系合成パルプ(三井化学(株)、SWP・E795)15重量%と、粉砕B型シリカゲル(新越化成工業(株)GB(W)30メッシュパス)70重量%と、さらにPP/PE系複合繊維1.7dt×3mm(チッソ(株)、インタック)15重量%の混合物を100g/m2となるようエアレイド法でウェブ層として形成した。さらにこの上部に、上記16g/m2のエアスルー不織布シートを上層シートとして載置して、これら複層シートを重ねたままで136℃の熱オーブンで熱風処理したのちに表面フラットな一対の金属ローラーで100℃、20kgf/cmで熱圧処理した。得られた目付け132g/m2の積層一体化不織布は、柔軟で粉漏れも無く、実用に耐える強度、表面耐摩耗性などを有し、吸湿性不織布として有用であった。
Example 2
First, PP (polypropylene) / PE-based composite fiber 2.2 dt × 51 mm (Chisso Corporation, ESC) is used as a raw material fiber, and a web having a basis weight of 16 g / m 2 is obtained by a card method. Heat-treated into a sheet. The air permeability of this sheet was 0.9 seconds. Next, using this sheet as a base sheet, 15% by weight of polyethylene-based synthetic pulp (Mitsui Chemicals Co., Ltd., SWP · E795) and crushed B-type silica gel (Shinetsu Kasei Co., Ltd. GB (W)) (30 mesh pass) A 70% by weight and further 15% by weight PP / PE composite fiber 1.7 dt × 3 mm (Chisso Corporation, Intac) mixture was formed as a web layer by the airlaid method to 100 g / m 2 . . Further, on the upper part, the above-mentioned 16 g / m 2 air-through non-woven sheet is placed as an upper layer sheet. After these multilayer sheets are stacked, hot air treatment is performed in a 136 ° C. hot oven, and then a pair of metal rollers with a flat surface is used. Hot pressing was performed at 100 ° C. and 20 kgf / cm. The obtained laminated integrated nonwoven fabric having a basis weight of 132 g / m 2 was flexible and free from powder leakage, had practical strength, surface wear resistance, etc., and was useful as a hygroscopic nonwoven fabric.
実施例3
目付け30g/m2、通気度1.4秒のPPスパンボンド(三井化学(株)、シンテックス)を基材シートとして、まずこの上に、PP/PE系複合繊維1.7dt×3(チッソ(株)、インタック)を10g/m2となるようエアレイド法でウェブを形成し、接着性不織布の層とした。次に、この上に、ポリエチレン系合成パルプ(三井化学(株)、SWP・E795)10重量%と、粉砕B型シリカゲル(新越化成工業(株)、GB(W)30メッシュパス)80重量%と、さらにPP/PE系複合繊維1.7dt×3mm(チッソ(株)、インタック)10重量%の混合物を320g/m2となるようエアレイド法でウェブ層として形成した。さらに、この上部に、PP/PE系複合繊維1.7dt×3(チッソ(株)、インタック)を10g/m2となるようエアレイド法でウェブを形成し、接着性不織布の層とした。さらに、この上部に上記30g/m2のPPスパンボンドを上層シートとして載置して、これら複層シートを重ねたままで138℃の熱オーブンで熱風処理したのちに表面フラットな一対の金属ローラーで60℃、10kgf/cmでカレンダー処理した。得られた目付け400g/m2の積層一体化不織布は、柔軟で粉漏れも無く、実用に耐える強度、表面耐摩耗性などを有し、吸湿性不織布として有用であった。
Example 3
Using PP spunbond (Mitsui Chemicals, Syntex) with a basis weight of 30 g / m 2 and an air permeability of 1.4 seconds as a base sheet, first, PP / PE composite fiber 1.7 dt × 3 (Chisso) A web was formed by an airlaid method so as to be 10 g / m 2 as an adhesive nonwoven fabric layer. Next, on top of this, polyethylene synthetic pulp (Mitsui Chemicals Co., Ltd., SWP · E795) 10% by weight and crushed B-type silica gel (Shinetsu Kasei Co., Ltd., GB (W) 30 mesh pass) 80% by weight % And a PP / PE composite fiber 1.7 dt × 3 mm (Chisso Corporation, Intac) 10 wt% mixture was formed as a web layer by the airlaid method so as to be 320 g / m 2 . Furthermore, a web was formed on the upper portion of the PP / PE composite fiber 1.7 dt × 3 (Chisso Corporation, Intac) by an airlaid method so as to be 10 g / m 2 , thereby forming an adhesive nonwoven fabric layer. Further, the above-mentioned 30 g / m 2 PP spunbond is placed on the upper part as an upper layer sheet, and these multi-layer sheets are stacked and heated in a hot oven at 138 ° C., and then a pair of metal rollers with a flat surface is used. Calendar treatment was performed at 60 ° C. and 10 kgf / cm. The obtained laminated integrated nonwoven fabric with a basis weight of 400 g / m 2 was flexible and free from powder leakage, had practical strength, surface wear resistance, etc., and was useful as a hygroscopic nonwoven fabric.
<注>
(1)通気度; JIS P8117ガーレ試験機を使用する透気度(秒)で表す。
(2)厚さ; 40g/cm2の荷重によった。
(3)吸湿試験; 検体10cm×10cm。予備乾燥90℃×24hののちデシケーター中で2h室温放冷し、その後所定温湿度のデシケーター中に24時間放置。重量変化を測定し、g/m2に換算した。
(4)放湿試験; 高湿度RH90%×24hの条件で吸湿させたのち、低湿度RH20%のデシケーター中に24時間放置して放湿、重量変化を測定して残存吸湿量をg/m2に換算した。
(5)粉漏れ; 10cm×10cmの検体をポリ袋に入れ、10秒間激しく振ったあとに袋内の粉体を観察した。「極く微量」とは1重量%以下、「極めて多い」とは10重量%超、を意味する。
<Note>
(1) Air permeability: Expressed in terms of air permeability (seconds) using a JIS P8117 Gurley tester.
(2) Thickness: According to a load of 40 g / cm 2 .
(3) Moisture absorption test; specimen 10 cm x 10 cm. After pre-drying 90 ° C. × 24 h, it is allowed to cool at room temperature in a desiccator for 2 h, and then left in a desiccator with a predetermined temperature and humidity for 24 hours. The change in weight was measured and converted to g / m 2 .
(4) Moisture release test; after absorbing moisture under the conditions of high humidity RH90% × 24h, letting it stand in a desiccator with low humidity RH20% for 24 hours to measure moisture release and change in weight to determine the residual moisture absorption g / m Converted to 2 .
(5) Powder leakage: A 10 cm × 10 cm specimen was placed in a plastic bag, shaken vigorously for 10 seconds, and then the powder in the bag was observed. “Very trace amount” means 1% by weight or less, and “very high” means more than 10% by weight.
本発明の吸湿性不織布は湿度調節や結露防止の機能を有する上に、吸湿性粉体の脱落がなく、柔軟性にも富むので、例えば脱酸素剤、乾燥剤、発熱剤、吸湿 剤、脱臭剤、防虫剤、除湿剤、芳香剤を収納した包装体等の商品に応用できる。さらに各種の建築材料、衛生材料、生活用材料、医薬・食品用部材、電機電子部品、電線材料などの広い範囲の用途に適用できる。
建築材料用途の具体例としては、壁内材、壁紙、屋根材、屋根下敷材、外装材、床材、カーペット部品、押入れシート、カーテン、ロールカーテン、仕切材などであり、衛生材料の具体例としては乳児用、大人用のおむつ部品、生理用品、メディカルガウン、手術用品、介護用シート、医療部材、介護用品物品などであり、生活用品としては押し入れ、タンスなどの除湿剤、医薬部材としては医薬品包装の除湿剤、食品部材としてはお菓子などの包装内部の除湿剤などがあげられる。
また、湿度を嫌う電機電子部品の包装ばかりでなく、複写機、映像機器などの電機電子機器の内部に取り付けて吸湿・湿度調節の機能を発揮することもできる。
The hygroscopic nonwoven fabric of the present invention has functions of humidity control and dew condensation prevention, and does not drop hygroscopic powder, and is also flexible.For example, an oxygen scavenger, desiccant, exothermic agent, hygroscopic agent, deodorant, etc. It can be applied to products such as packages containing insecticides, insect repellents, dehumidifiers and fragrances. Furthermore, it can be applied to a wide range of uses such as various building materials, hygiene materials, daily life materials, pharmaceutical / food materials, electrical and electronic parts, and electric wire materials.
Specific examples of building material applications include interior materials, wallpaper, roofing materials, roof covering materials, exterior materials, flooring materials, carpet parts, closet sheets, curtains, roll curtains, partition materials, etc. As diaper parts for infants, adults, sanitary products, medical gowns, surgical supplies, care sheets, medical materials, care products, etc. Examples of the dehumidifying agent for pharmaceutical packaging and the food member include a dehumidifying agent inside a package such as sweets.
In addition to packaging of electrical and electronic parts that dislike humidity, it can also be mounted inside electrical and electronic equipment such as copying machines and video equipment to exhibit moisture absorption and humidity control functions.
Claims (7)
The hygroscopic nonwoven fabric according to any one of claims 1 to 6, which is heat-treated.
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| JP2005115208A JP4671741B2 (en) | 2005-04-13 | 2005-04-13 | Hygroscopic nonwoven fabric |
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| JP2005115208A JP4671741B2 (en) | 2005-04-13 | 2005-04-13 | Hygroscopic nonwoven fabric |
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| JP2006291404A true JP2006291404A (en) | 2006-10-26 |
| JP4671741B2 JP4671741B2 (en) | 2011-04-20 |
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| JP2005115208A Expired - Fee Related JP4671741B2 (en) | 2005-04-13 | 2005-04-13 | Hygroscopic nonwoven fabric |
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| JP2009039905A (en) * | 2007-08-07 | 2009-02-26 | Dainippon Printing Co Ltd | Moisture-absorbing laminate and water-absorbing pouch using the same |
| JP2009040440A (en) * | 2007-08-07 | 2009-02-26 | Dainippon Printing Co Ltd | Oxygen moisture-absorbing pouch and packaging product using the same |
| JP2009136863A (en) * | 2007-11-14 | 2009-06-25 | Nitto Denko Corp | Filter medium, method for manufacturing the same, and filter unit |
| JP2010106402A (en) * | 2008-10-31 | 2010-05-13 | Kinsei Seishi Kk | Water-permeable nonwoven fabric sheet |
| JP2011245719A (en) * | 2010-05-26 | 2011-12-08 | Nissan Motor Co Ltd | Resin molding containing bamboo fiber, and method and apparatus for manufacturing the same |
| CN116590846A (en) * | 2023-07-11 | 2023-08-15 | 江苏青昀新材料有限公司 | Flash-spun polyethylene film material with better toughness and manufacturing method thereof |
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| JP2004115927A (en) * | 2002-09-20 | 2004-04-15 | Mitsui Chemicals Inc | Wallpaper |
| JP2004216217A (en) * | 2003-01-10 | 2004-08-05 | Toppan Printing Co Ltd | Method for producing moisture absorbing and releasing material |
| JP2004262022A (en) * | 2003-02-28 | 2004-09-24 | Chisso Corp | Functional fiber aggregate and molded body using the same |
| JP2005067023A (en) * | 2003-08-25 | 2005-03-17 | Kinsei Seishi Kk | Laminated and integrated water absorption mat for food |
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| WO2002000983A1 (en) * | 2000-06-26 | 2002-01-03 | Matsumoto Yushi-Seiyaku Co., Ltd. | Functional non-woven fabric |
| JP2002235268A (en) * | 2000-12-06 | 2002-08-23 | Japan Vilene Co Ltd | Powder-bonded nonwoven fabric, method for producing the same, and sheet material containing the same |
| JP2004115927A (en) * | 2002-09-20 | 2004-04-15 | Mitsui Chemicals Inc | Wallpaper |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2009039905A (en) * | 2007-08-07 | 2009-02-26 | Dainippon Printing Co Ltd | Moisture-absorbing laminate and water-absorbing pouch using the same |
| JP2009040440A (en) * | 2007-08-07 | 2009-02-26 | Dainippon Printing Co Ltd | Oxygen moisture-absorbing pouch and packaging product using the same |
| JP2009136863A (en) * | 2007-11-14 | 2009-06-25 | Nitto Denko Corp | Filter medium, method for manufacturing the same, and filter unit |
| US8900351B2 (en) | 2007-11-14 | 2014-12-02 | Nitto Denko Corporation | Filter medium and method of manufacturing the same and filter unit |
| JP2010106402A (en) * | 2008-10-31 | 2010-05-13 | Kinsei Seishi Kk | Water-permeable nonwoven fabric sheet |
| JP2011245719A (en) * | 2010-05-26 | 2011-12-08 | Nissan Motor Co Ltd | Resin molding containing bamboo fiber, and method and apparatus for manufacturing the same |
| CN116590846A (en) * | 2023-07-11 | 2023-08-15 | 江苏青昀新材料有限公司 | Flash-spun polyethylene film material with better toughness and manufacturing method thereof |
| CN116590846B (en) * | 2023-07-11 | 2023-10-20 | 江苏青昀新材料有限公司 | Flash-spun polyethylene film material with better toughness and manufacturing method thereof |
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| JP4671741B2 (en) | 2011-04-20 |
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