JPH02143847A - Laminated nonwoven fabric - Google Patents
Laminated nonwoven fabricInfo
- Publication number
- JPH02143847A JPH02143847A JP63297017A JP29701788A JPH02143847A JP H02143847 A JPH02143847 A JP H02143847A JP 63297017 A JP63297017 A JP 63297017A JP 29701788 A JP29701788 A JP 29701788A JP H02143847 A JPH02143847 A JP H02143847A
- Authority
- JP
- Japan
- Prior art keywords
- nonwoven fabric
- stress
- elongation
- laminated
- synthetic fiber
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004745 nonwoven fabric Substances 0.000 title claims abstract description 127
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 34
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 34
- 229920003051 synthetic elastomer Polymers 0.000 claims abstract description 24
- 239000005061 synthetic rubber Substances 0.000 claims abstract description 24
- 238000011084 recovery Methods 0.000 claims abstract description 13
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims abstract description 8
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 8
- 229920000098 polyolefin Polymers 0.000 claims abstract description 7
- 230000000704 physical effect Effects 0.000 claims abstract description 6
- 230000008602 contraction Effects 0.000 claims abstract description 3
- 238000003475 lamination Methods 0.000 claims description 2
- 238000010030 laminating Methods 0.000 abstract description 4
- 239000000835 fiber Substances 0.000 description 29
- 239000002131 composite material Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 16
- 238000010438 heat treatment Methods 0.000 description 8
- 239000004814 polyurethane Substances 0.000 description 8
- 229920002635 polyurethane Polymers 0.000 description 8
- 230000037303 wrinkles Effects 0.000 description 8
- 229920001971 elastomer Polymers 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000005060 rubber Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- -1 polypropylene Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 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
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000004049 embossing Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000000386 athletic effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000002788 crimping Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 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
- 239000004970 Chain extender Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 210000000707 wrist Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、積層不織布に関する。さらに詳しくは伸縮性
、風合い、柔軟性に優れ、シワができにくいなど外観に
優れる積層不織布に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a laminated nonwoven fabric. More specifically, it relates to a laminated nonwoven fabric that has excellent elasticity, texture, and flexibility, and has an excellent appearance such as wrinkle resistance.
サポータ、包帯、パップ剤の基布に用いられる伸縮性不
織布は、従来からポリウレタン不織布が各種あり(特開
昭59−223347号)、合成ゴム糸からなる布綿と
不織布シートを一体にした伸縮性を有する不織布(特開
昭flft−201060号)などが知られている。Stretchable nonwoven fabrics used as base fabrics for supporters, bandages, and poultices have traditionally been made of polyurethane nonwoven fabrics (Japanese Patent Application Laid-open No. 59-223347). A nonwoven fabric having the following properties (Japanese Patent Application Laid-Open No. 2010-201060) is known.
ゴム系不織布をサポータ−などに使用した場合、伸縮性
が大きいため身体に密着するものの、伸長応力が大きす
ぎるものは圧迫を与え、運動時に拘束があり、身体の運
動能力を100%発揮できるものではない。ここで述べ
る伸縮性が大きいとは、充分に伸びるとともに30%伸
縮繰り返し後の弾性回復率が大きいものをいい、伸長応
力とは、後記の条件で測定した、3゛0%伸長時の応力
であり、不織布の巾1011当りの応力を不織布の目付
けで割った値である。このようなゴム系からなる一般的
な不織布では、伸縮性があるとともに伸長応力が2〜3
0 g/cm//g/+/もある。When rubber-based nonwoven fabrics are used for supports, etc., they have high elasticity and adhere closely to the body, but if the stretching stress is too large, they will put pressure on you and restrict you during exercise, making it impossible to fully demonstrate your body's athletic ability. isn't it. High elasticity mentioned here refers to one that is sufficiently elongated and has a large elastic recovery rate after repeated 30% elongation, and elongation stress is the stress at 30% elongation measured under the conditions described below. It is the value obtained by dividing the stress per width 1011 of the nonwoven fabric by the basis weight of the nonwoven fabric. General non-woven fabrics made of such rubber-based materials have elasticity and an elongation stress of 2 to 3.
There is also 0 g/cm//g/+/.
またゴム系不織布を中間目とし、その両面に不織布シー
トを積層した伸縮性不織布がある。しかし−膜内に使用
する不織布シートは、伸縮性がなく、伸長時の応力が大
きく、30%伸長時の応力が10〜100 g/am/
/g/Fもある。このような伸縮性のない不織布シート
を積層した不織布においては、伸長応力を低下させるも
のではない。伸長応力の改善されない積層不織布では、
応力、圧迫感、運動時の自由性を充分に改善されるもの
ではなく、繰り返し使用するとシワが発生する。また熱
可塑性ポリウレタン不織布を縦、横方向に伸長し、その
状態でポリエステル繊維等のカードウェブ等を積層し熱
圧着し、その後伸長を開放する方法よる伸縮性不織布が
ある。このような積層不織布においてもシワが発生し、
表面の均一性に劣るという欠点がある。In addition, there is a stretchable nonwoven fabric in which a rubber nonwoven fabric is used as an intermediate mesh, and nonwoven fabric sheets are laminated on both sides of the fabric. However, the nonwoven fabric sheet used in the membrane has no elasticity and has a large stress when stretched, with a stress of 10 to 100 g/am/ when stretched by 30%.
/g/F is also available. In a nonwoven fabric made by laminating such non-stretchable nonwoven fabric sheets, the elongation stress is not reduced. In laminated nonwoven fabrics whose elongation stress is not improved,
It does not sufficiently improve stress, pressure, and freedom of movement, and wrinkles occur when used repeatedly. There is also a stretchable nonwoven fabric produced by stretching a thermoplastic polyurethane nonwoven fabric in the vertical and horizontal directions, laminating a card web of polyester fiber or the like in that state, thermally pressing the fabric, and then releasing the stretching. Wrinkles also occur in such laminated nonwoven fabrics,
It has the disadvantage of poor surface uniformity.
本発明の目的は、風合いが良く、伸縮性が大きくても伸
長応力が小さく、かつ柔軟性があり、シワができにくく
表面の均一性に優れた積層不織布を提供することにある
。An object of the present invention is to provide a laminated nonwoven fabric that has a good feel, has low elongation stress even if it has high elasticity, is flexible, and is resistant to wrinkles and has an excellent surface uniformity.
すなわち本願の発明は、合成ゴム系不織布と合成繊維系
不織布を積層した不織布において、伸縮性で低伸長応力
の合成繊維系不織布を用いた積層不織布である。That is, the invention of the present application is a laminated nonwoven fabric in which a synthetic rubber nonwoven fabric and a synthetic fiber nonwoven fabric are laminated, using a synthetic fiber nonwoven fabric that is stretchable and has low elongation stress.
本発明の合成繊維系不織布とは、伸縮性があり、伸長応
力の低い合成繊維からなる不織布であることが必要であ
る。−膜内な不織布は、伸縮性がなく本発明の合成繊維
系不織布には適さない。また伸縮性のある不織布、例え
ばゴム繊維からなる不織布は、伸縮性があるとともに伸
長時の応力が大きく、本発明の合成繊維系不織布には適
さない。The synthetic fiber nonwoven fabric of the present invention needs to be a nonwoven fabric made of synthetic fibers that is stretchable and has low elongation stress. - Membrane nonwoven fabrics have no elasticity and are not suitable for the synthetic fiber nonwoven fabric of the present invention. In addition, a stretchable nonwoven fabric, for example, a nonwoven fabric made of rubber fibers is stretchable and generates large stress when stretched, and is therefore not suitable for the synthetic fiber nonwoven fabric of the present invention.
本発明の合成繊維系不織布は伸縮性があることが必要で
ある。この伸縮性は、80%以上あることが好ましい。The synthetic fiber nonwoven fabric of the present invention needs to be stretchable. This stretchability is preferably 80% or more.
また本発明の合成繊維系不織布は、伸長応力が低く、3
0%伸長時の応力が2〜0.1g/am//g/−であ
ることが好ましい。合成繊維系不織布の弾性回復率が8
0%以下の場合、積層不織布の伸縮性を低下するので好
ましくない。合成繊維系不織布の伸長応力が2 g/a
m//g/nF以上の場合には、積層不織布の伸長応力
を大きくすることがあり好まない。伸縮性があり伸長応
力のある合成繊維系不織布を用いた積層不織布は、サポ
ータ−などに使用した場合、人体に与える負荷が大きす
ぎるので適さない。Furthermore, the synthetic fiber nonwoven fabric of the present invention has low elongation stress and 3
It is preferable that the stress at 0% elongation is 2 to 0.1 g/am//g/-. The elastic recovery rate of synthetic fiber nonwoven fabric is 8
If it is less than 0%, it is not preferable because the elasticity of the laminated nonwoven fabric decreases. The elongation stress of synthetic fiber nonwoven fabric is 2 g/a
If it is more than m//g/nF, the elongation stress of the laminated nonwoven fabric may increase, which is not preferable. A laminated nonwoven fabric using a synthetic fiber nonwoven fabric that is stretchable and has elongation stress is not suitable when used for a supporter or the like because it imposes too large a load on the human body.
本発明の合成繊維系不織布とは、特定な伸縮性があり、
伸長応力の低い合成繊維からなる不織布であればその繊
維は、ポリオレフィン、ポリアミド、ポリエステルなど
の合成繊維からなるものであっても、またこれらとレー
ヨン、木綿、麻これらの混合されたものでもよく、製品
の風合、吸水性改良等の目的で混合されるが、ポリオレ
フィンからなるものが好ましい。The synthetic fiber nonwoven fabric of the present invention has specific elasticity,
If it is a nonwoven fabric made of synthetic fibers with low elongation stress, the fibers may be made of synthetic fibers such as polyolefin, polyamide, polyester, or a mixture of these with rayon, cotton, hemp, etc. It is mixed for the purpose of improving the texture and water absorption of the product, but it is preferably made of polyolefin.
さらに詳しくポリオレフィンからなる複合繊維を用いた
合成繊維系不織布を説明する。この複合繊維としては並
列型、鞘芯型あるいは繊維断面が円形以外の異形状の複
合繊維があり、この複合繊維の具体例として、第1成分
ポリオレフィンとして、MFR(メルトフローレート)
が2〜70の結晶性ポリプロピレン、好ましくは分子全
分布の指標のQ値(Mw/′gin)が5.5以下のプ
ロヒレンホモボリマーが用いられる。第2成分の低1独
点ポリオレフィンとしては、プロピレンを主成分として
エチレン、ブテン−1等の他のα−オレフィンを共重合
成分とする2元系、或いは3元系の共重合体、好ましく
は第1成分より融点が15°C以上低い共重合体が用い
られる。この両成分の選択、組み合せ、及び紡糸、延伸
条件の選択により熱処理したときに繊維の捲縮収縮、熱
収縮等が発生し、不織布としたときに、所望の弾性回復
率、伸長応力とすることができる。In more detail, a synthetic fiber nonwoven fabric using composite fibers made of polyolefin will be explained. These composite fibers include parallel type, sheath-core type, and composite fibers with irregularly shaped fiber cross sections other than circular.As a specific example of this composite fiber, as the first component polyolefin, MFR (melt flow rate)
Crystalline polypropylene having a molecular weight of 2 to 70, preferably a prohylene homopolymer having a Q value (Mw/'gin), which is an index of the total molecular distribution, of 5.5 or less is used. The second component, the low uniqueness polyolefin, is preferably a binary or ternary copolymer containing propylene as the main component and other α-olefins such as ethylene and butene-1 as copolymer components. A copolymer having a melting point 15°C or more lower than that of the first component is used. The selection and combination of these two components, as well as the selection of spinning and drawing conditions, causes crimping and thermal contraction of the fibers when heat-treated, resulting in the desired elastic recovery rate and elongation stress when made into a nonwoven fabric. Can be done.
本発明の合成繊維系不織布の製法は、公知の不織布化の
方法であればよく、特に限定されるものではないが特開
昭[13−28980号公報記載のようなウォーターニ
ードル法により得ることができる。この場合、合成繊維
をカード法でウェブとし、このウェブをさらにウォータ
ーニードル結合等の処理により密に結合し、ウェブは、
無緊張状態で搬送されながら、表裏両面より熱風により
加熱される方式の熱処理機で熱処理する。この熱処理に
よりウェブ収縮を発生せしめ、ウェブ収縮と同時に合成
繊維の融着により繊維の交点が部分的に熱接着し、伸縮
性があり、伸長応力の低い合成繊維系不織布になる。こ
の不織布化以外の気流式ランダムウニバー法、湿式抄紙
法等の公知の方法が利用でき、更にクロスラッパーを用
いてクロスラッパーウェブとしてもよい。ウェブをさら
にニードルパンチ結合等の処理により密に結合してもよ
い。ウェブは、無緊張状態で搬送されながら、ウェブの
熱収縮を損わないような機能を有する熱処理機で熱処理
してもよい。不織布をさらに、熱エンボスロールで熱圧
着面積的5〜50%に熱圧着することも可能である。The method for producing the synthetic fiber nonwoven fabric of the present invention may be any known method for producing a nonwoven fabric, and is not particularly limited. can. In this case, the synthetic fibers are made into a web using a carding method, and this web is further tightly bonded by a process such as water needle bonding.
While being conveyed without tension, it is heat treated in a heat treatment machine that heats both the front and back sides with hot air. This heat treatment causes web shrinkage, and at the same time as the web shrinks, the synthetic fibers are fused and the intersections of the fibers are partially thermally bonded, resulting in a synthetic fiber nonwoven fabric with elasticity and low elongation stress. Other than this non-woven fabric, known methods such as the air flow random univer method and the wet paper making method can be used, and furthermore, a cross wrapper may be used to form a cross wrapper web. The webs may be further bonded tightly by processes such as needle punch bonding. The web may be heat-treated in a heat-treating machine having a function that does not impair the thermal shrinkage of the web while being conveyed in a tension-free state. It is also possible to further thermocompress the nonwoven fabric to an area of 5 to 50% using a thermoemboss roll.
本発明において合成ゴム系不織布とは、伸縮性のある合
成ゴムを原料とした繊維の不織布である。In the present invention, the synthetic rubber nonwoven fabric is a nonwoven fabric made of fibers made from stretchable synthetic rubber.
この合成ゴムとしてはポリウレタン系、ポリエステル系
、ポリアミド系、フッ素系などを挙げることができ、ポ
リウレタン系なかでも、熱可塑性ポリウレタン系が好ま
しい。Examples of this synthetic rubber include polyurethane-based, polyester-based, polyamide-based, fluorine-based, etc. Among polyurethane-based rubbers, thermoplastic polyurethane-based rubbers are preferred.
この熱可塑性ポリウレタンは、分子中にウレタン結合、
ウレア結合を有する広義のポリウレタンであって、溶融
紡糸可能な熱可塑性ポリウレタンを溶融紡糸し不織布化
したものである。原料ポリウレタンは溶融紡糸が可能で
あれば線状ポリウレタンであっても、架橋ポリウレタン
であってもいづれでもよい。例えば、ジヒドロキシポリ
エーテル、ジヒドロキシポリエステル等の分子ff15
00〜6000のポリオールと、P、Pジフェニルメタ
ンジイソシアネート、トリレンジイソシアネート、テト
ラメチレンジイソシアネート、ヘキサメチレンジイソシ
アネート、キシレンジイソシアネート等の分子量800
以下の有機ジイソシアネートとモドラジン、ジアミン、
グリコール等の鎖伸長剤との反応によって得られるポリ
ウレタンの中から選ぶことができる。This thermoplastic polyurethane has urethane bonds in the molecule,
Polyurethane in a broad sense has urea bonds, and is made by melt-spinning thermoplastic polyurethane that can be melt-spun into a non-woven fabric. The raw material polyurethane may be linear polyurethane or crosslinked polyurethane, as long as it can be melt-spun. For example, molecules ff15 such as dihydroxy polyether, dihydroxy polyester, etc.
Polyols with a molecular weight of 00 to 6000 and P, P diphenylmethane diisocyanate, tolylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate, xylene diisocyanate, etc. with a molecular weight of 800
The following organic diisocyanates and modrazine, diamines,
It can be chosen among polyurethanes obtained by reaction with chain extenders such as glycols.
合成ゴム系繊維の不織布化は、合成ゴムを溶融紡糸しス
パンボンド法、メルトブロー法等でウェブ又は不織布と
し、さらに熱圧着処理、乾熱処理等と組合せて得ること
ができる。また溶融紡糸した繊維をカード法ウェブ、湿
式抄紙法ウェブとしさらに公知の方法で加熱処理するこ
とにより得ることもでき特に不織布化を限定するもので
はない。Synthetic rubber fibers can be made into a non-woven fabric by melt-spinning synthetic rubber to form a web or non-woven fabric using a spunbond method, a melt-blowing method, etc., and further combining the process with a thermocompression bonding treatment, a dry heat treatment, etc. Further, the melt-spun fibers can be made into a carded web or a wet papermaking web and further heat-treated by a known method to obtain the fibers, and there is no particular limitation on the formation of non-woven fabrics.
この合成ゴム系不織布を構成する繊維の好ましいデニー
ルは1〜500/r、さらに好ましくは1〜30d/f
である。デニールが小の程風合は柔軟性が良くなる。ま
た合成ゴム系不織布の好ましい目付はlO〜300 g
/♂である。不織布目付が10g/rl以下では、不織
布の均一性が劣り、300g/♂以上では風合いが恕く
好まれない。本発明の収縮性ある合成ゴム系不織布は、
合成ゴム系繊維からなることが必要であり、合成ゴム系
繊維が70%以上あることが好ましく、さらに100%
であるとより好ましい。またこの合成ゴム系不織布は3
09A伸長後の弾性回復率で80%以上が好ましく、さ
らに90%以上であることがより好ましい。The preferred denier of the fibers constituting this synthetic rubber nonwoven fabric is 1 to 500 d/f, more preferably 1 to 30 d/f.
It is. The smaller the denier, the more flexible the texture. In addition, the preferred basis weight of the synthetic rubber nonwoven fabric is lO~300 g.
/It is a male. If the nonwoven fabric weight is less than 10 g/rl, the uniformity of the nonwoven fabric will be poor, and if it is more than 300 g/rl, the texture will be poor and undesirable. The shrinkable synthetic rubber nonwoven fabric of the present invention is
It is necessary to consist of synthetic rubber fibers, preferably 70% or more, and more preferably 100% synthetic rubber fibers.
It is more preferable. In addition, this synthetic rubber nonwoven fabric has 3
The elastic recovery rate after 09A elongation is preferably 80% or more, and more preferably 90% or more.
本発明の積層不織布の積層方法は、合成ゴム系不織布と
合成繊維系不織布を二層にまた多層状に積重ね、それを
熱カレンダーロール、熱エンボスロール等を用い熱接着
温度以上の温度で熱圧着する方法を例示できるが、これ
に限定するものではなく、積層できる公知方法であって
もよい。この熱エンボスロール法の場合、圧着面積は約
5〜50%が好ましい。また、乾熱、或いは湿熱式加熱
機を用い、積層不織布の境界面に熱接骨が起るような熱
風温度、加熱時間等の条件を選択し積層不織布とするこ
ともできる。The method for laminating the laminated nonwoven fabric of the present invention involves stacking a synthetic rubber nonwoven fabric and a synthetic fiber nonwoven fabric in two or multiple layers, and then thermocompression bonding using a heat calendar roll, heat embossing roll, etc. at a temperature higher than the heat bonding temperature. Examples of methods for doing this include, but the present invention is not limited to this, and any known method that allows lamination may be used. In the case of this hot embossing roll method, the crimping area is preferably about 5 to 50%. Alternatively, a laminated nonwoven fabric can be formed by using a dry heat or wet heat heating machine and selecting conditions such as hot air temperature and heating time that cause thermal bonding to occur at the interface of the laminated nonwoven fabric.
本発明の積層不織布は、特定な合成ゴム系不織布と、伸
縮性で低伸長応力の合成繊維系不織布を用いた積層不織
布なので、1)伸縮性がありながら、同時に伸長応力を
下げることがでる。このため2)風合い、3)柔軟性に
優れ、4)シワができにくいなど外観に優れた積層不織
布となり、5)運動時に身体の拘束がなく、運動能力を
充分に発揮できる従来にない格別な効果のある積層不織
布である。The laminated nonwoven fabric of the present invention is a laminated nonwoven fabric using a specific synthetic rubber nonwoven fabric and a synthetic fiber nonwoven fabric that is stretchable and has low elongation stress, so 1) it has elasticity and can simultaneously reduce elongation stress. This results in a laminated non-woven fabric with 2) excellent texture, 3) flexibility, 4) excellent appearance such as wrinkle resistance, and 5) an unprecedented and exceptional material that allows you to fully demonstrate your athletic abilities without restricting your body during exercise. It is an effective laminated nonwoven fabric.
本発明の積層不織布は、目付15〜150g/♂の低目
付のものでは包帯、紙おしめの表面材、紙おしめの裏面
材等の用途に、150〜300g/−Pの高目付のもの
では、衣料用芯地、各種のストレッチ用材料等の用途に
有用である。The laminated nonwoven fabric of the present invention has a low basis weight of 15 to 150 g/♂ for applications such as bandages, surface materials for paper diapers, backing materials for paper diapers, etc., and those with a high basis weight of 150 to 300 g/-P can be used as It is useful for applications such as interlining for clothing and various stretch materials.
実施例及び比較例により本発明をさらに具体的に説明す
る。なお各個で用いた物性測定方法を一括して以下に示
す。The present invention will be explained in more detail with reference to Examples and Comparative Examples. The physical property measurement methods used for each are listed below.
風合:得られた積層不織布から手ざわりの風合いを調べ
た。Texture: The texture of the obtained laminated nonwoven fabric was examined.
伸長窓カニ各種不織布の縦方向の長さ15cm1幅2.
5cmの試料片を切り取り、定速伸長型の自記式引張試
験器を用い、つかみ間隔10cm1引張速度10cm/
■−で3cmだけ伸長し30%伸長時の強力を測定した
記録紙より読み取る(このと壽の強力をα(g)とする
)。5個の試料の平均値をとり、さらに試料の幅1cm
当りで且つ試料の目付で割った値とした。 (試料の幅
1c鳳で且つ目付がIg//当りに換算した値)
伸長窓カニα(g)/2.5(am)/1♂当りの目付
(g/F)(g /cta//g /+/ )
弾性回復率: 30%伸長応力を測定しそのまま1分間
放置後、lOc■/llll11の速度で弛緩させる。Elongated window crab Various non-woven fabric length 15 cm 1 width 2.
A 5 cm sample piece was cut out and tested using a constant speed extension type self-recording tensile tester at a grip interval of 10 cm and a tensile speed of 10 cm/
(2) The strength at 30% extension after being extended by 3 cm at - is read from the recording paper (the strength at this time is defined as α (g)). Take the average value of 5 samples, and further measure the width of the sample by 1 cm.
The value was determined by the hit and divided by the basis weight of the sample. (Value converted to sample width 1c and basis weight per Ig//) Elongated window crab α (g) / 2.5 (am) / basis weight per 1 male (g/F) (g /cta// g /+/ ) Elastic recovery rate: Measure the 30% elongation stress, leave it as it is for 1 minute, and then relax at a rate of lOc/llll1.
この弛緩の過程で応力が零になった時点の残存伸び(A
auw)を記録紙より読み取り、1回測定後1分間放置
し繰返し5回の測定を行なった。下式より5個の試料の
平均値で算出し表わす。The residual elongation (A
auw) was read from the recording paper, and after one measurement, the sample was left for 1 minute and the measurement was repeated five times. It is calculated and expressed as the average value of 5 samples using the formula below.
シワ:弾性回復率で測定した後の試料を平地に放置し1
時1m後のシワの育無を調べた。Wrinkle: After measuring the elastic recovery rate, leave the sample on a flat surface and
The growth of wrinkles was examined after 1 m.
柔軟性:得られた積層不織布を、手首にするサポータ状
に縫製し運動使用時の拘束性、圧迫感を調べた。Flexibility: The obtained laminated nonwoven fabric was sewn into a supporter shape for the wrist, and its restraint and pressure feeling during exercise were examined.
〔実施例−1〜6〕
合成ゴム系不織布として、以下に示す熱可塑性ポリウレ
タン2種を用いた。脂肪族ポリイソシアネートとポリエ
ーテルポリオールの反応により得られたものを加熱溶融
し、スパンボンド法で紡糸しウェブを熱カレンダロール
で熱圧着することにより得たもの(G−1)。脂肪族ポ
リイソシアネートと、ポリエステルポリオールの反応に
より得られた熱可塑性ポリウレタンを加熱溶融し、メル
トブロー法で紡糸しウェブを部分的に熱接骨し、さらに
カレンダロールで熱圧着することにより得たもの(G−
2)。[Examples 1 to 6] Two types of thermoplastic polyurethanes shown below were used as synthetic rubber nonwoven fabrics. A product obtained by heating and melting a product obtained by the reaction of an aliphatic polyisocyanate and a polyether polyol, spinning it using a spunbond method, and thermocompressing the web using a thermocalender roll (G-1). A thermoplastic polyurethane obtained by the reaction of an aliphatic polyisocyanate and a polyester polyol is heated and melted, the web is spun using a melt blowing method, the web is partially heat-bonded, and the web is further thermocompressed using a calender roll (G −
2).
合成繊維系不織布として以下に示す5種を用いた。The following five types of synthetic fiber nonwoven fabrics were used.
F−1: MFR8,5、分子量分布の指標Qが5゜O
のポリプロピレンを第1成分とし、MFR8、プロピレ
ン/エチレンランダムコポリマー(Ci”97.5vt
%、C2” 2.5vt%)軟化点130℃、融点14
5℃を第2成分とし、複合比50対50の並列型複合繊
維、該複合繊維を用いランダムウェブとし、熱風噴出型
加熱機を用い、温度140℃でウェブを無緊張下で熱処
理し、ウェブ収縮率を54%発生させ、捲縮の絡合及び
繊維の交点で部分的な熱接着をさせることにより得たも
の。F-1: MFR8.5, molecular weight distribution index Q 5°O
polypropylene as the first component, MFR8, propylene/ethylene random copolymer (Ci”97.5vt
%, C2” 2.5vt%) Softening point 130℃, Melting point 14
5°C as the second component, a parallel composite fiber with a composite ratio of 50:50, a random web using the composite fiber, heat treatment of the web at a temperature of 140°C under no tension using a hot air jet heating machine, and a web Obtained by generating a shrinkage rate of 54% and performing partial thermal bonding at the entanglement of crimps and the intersection of fibers.
F−2:第1成分はF−1と同一のポリプロピレンとし
、第2成分をプロピレン/エチレン/ブテン−1(Ca
” 92wt%、Ct’ 3.5vt%、 Cm’
4.5冒t%)MFR12,5、軟化点110℃、融点
目O″Cを用い、複合比、複合形態はF−1と同一の複
合繊維とした。この繊維を用い、ウェブ形成及び不織布
化処理は、温度を130°Cとした以外はF−1と同一
条件とし不織布を得た。F-2: The first component is the same polypropylene as F-1, and the second component is propylene/ethylene/butene-1 (Ca
"92wt%, Ct' 3.5vt%, Cm'
4.5%) MFR 12.5, softening point 110°C, melting point O''C were used, and the composite ratio and composite form were the same as F-1. Using this fiber, web formation and nonwoven fabric were made. A nonwoven fabric was obtained under the same conditions as F-1 except that the temperature was 130°C.
ウェブの絡合及び繊維の交点で部分的な熱接骨を有し、
ウェブ収縮率は62%であった。having partial thermal bone bonding at web entanglements and fiber intersections;
Web shrinkage was 62%.
F−3=第1成分、第2成分及び複合比、複合形態等は
F−2と同一とし、但し、繊度は 3.OD/fであり
、この複合繊維を用い、ランダムウェーブとし−Hウオ
ーターニードル処理をした後、温度135°Cとした以
外はF−1と同一条件に準じ不織布を得た。F-3 = The first component, second component, composite ratio, composite form, etc. are the same as F-2, but the fineness is 3. OD/f, and using this composite fiber, a nonwoven fabric was obtained under the same conditions as F-1 except that the temperature was 135° C. after being subjected to a -H water needling treatment as a random wave.
F−4=第1成分はF−1と同一のポリプロピレンを用
い、第2成分をIIDPE(MFR20、融点132℃
)を用い、複合比、複合形態はF−1と同一の複合繊維
を得た。この繊維を用いカード機でパラレルウェブとし
た。続いて145℃で加熱処理し繊維の交点が強固に熱
接着した不織布を得た。F-4 = The first component uses the same polypropylene as F-1, and the second component is IIDPE (MFR 20, melting point 132 ° C.
), a composite fiber having the same composite ratio and composite form as F-1 was obtained. This fiber was made into a parallel web using a card machine. Subsequently, it was heat-treated at 145°C to obtain a nonwoven fabric in which the fiber intersections were firmly thermally bonded.
この不織布のウェブ収縮率は8%であった。The web shrinkage rate of this nonwoven fabric was 8%.
また伸縮性は30%伸長後の弾性回復率で60%以下と
低いものであった。Furthermore, the elasticity was low, with an elastic recovery rate of 60% or less after 30% elongation.
F−5:第1成分はポリエステルを用い、第2成分をH
DPE (M F R20、融点132℃)を用い、複
合比、複合形態はF−1と同一の複合繊維を得た。F-5: The first component is polyester, the second component is H
Using DPE (MFR20, melting point 132°C), a composite fiber having the same composite ratio and composite form as F-1 was obtained.
この繊維を用いカード機でパラレルウェブとした。This fiber was made into a parallel web using a card machine.
続いて145℃で加熱処理し繊維の交点が強固に熱接着
した不織布を得た。この不織布のウェブ収縮率は8%で
あった。また伸縮性は30%伸長後の弾性回復率で60
%以下と低いものであった。Subsequently, it was heat-treated at 145°C to obtain a nonwoven fabric in which the fiber intersections were firmly thermally bonded. The web shrinkage rate of this nonwoven fabric was 8%. In addition, the elasticity is 60% with elastic recovery rate after 30% elongation.
% or less.
前記した、合成ゴム系不織布の物性を第1表に示し合成
繊維系不織布の物性を第2表に示す。The physical properties of the synthetic rubber nonwoven fabric described above are shown in Table 1, and the physical properties of the synthetic fiber nonwoven fabric are shown in Table 2.
M4層不織布は、以下に記載する方法で行った。The M4 layer nonwoven fabric was prepared by the method described below.
合成ゴム系不織布と合成繊維系不織布を用い3居又は2
層構造とした。この不織布を、上部が凸部面積21%、
温度 110℃の熱エンボスロール下部が室温の金属ロ
ールを用い熱圧着し、エンボス部が熱接着した不織布(
実施例L 2.3.4、比較例1)とした。また11
0 〜125℃のカレンダロールで熱圧着し、不織布の
境界面で熱接着した不織布(実施例5.6、比較例2)
とした。3 or 2 using synthetic rubber non-woven fabric and synthetic fiber non-woven fabric
It has a layered structure. The upper part of this nonwoven fabric has a convex area of 21%,
The lower part of the heat embossing roll at a temperature of 110°C is thermocompressed using a metal roll at room temperature, and the embossed part is heat bonded to a nonwoven fabric (
Example L 2.3.4 and Comparative Example 1). Also 11
Nonwoven fabrics that were thermocompressed using a calendar roll at 0 to 125°C and thermally bonded at the interface of the nonwoven fabrics (Example 5.6, Comparative Example 2)
And so.
これらにより得られた積層不織布の物性を、表−3に示
す。Table 3 shows the physical properties of the laminated nonwoven fabrics obtained.
表−3より以下のことが判る。The following can be seen from Table 3.
合成ゴム系不織布と伸縮性で低伸長応力の合成繊維系不
織布を用いた積層不織布は、3層構造であっても(実施
例−1,2,3,4)、2層構造であっても(実施例−
5、θ)いずれも30%伸長弾性回復率は90%以上と
高く、且つ30%伸長応力は3 g/am//g/ r
l以下と小さいことが判る。一方、本発明以外の、合成
ゴム系不織布と伸縮性がなく伸長応力大きな合成繊維系
不織布を用いた積層不織布(比較例−1,2)は、30
%伸長応力が高く、弾性回復率も低い。このため積層不
織布の風合いが悪く、縁り返し伸縮をすることにより不
織布内部の構造亀裂が起きたためか、シワが発生し、サ
ポータ−として使用すると、運動拘束感があり柔軟性に
乏しいものであった。A laminated nonwoven fabric using a synthetic rubber nonwoven fabric and a synthetic fiber nonwoven fabric with elasticity and low elongation stress can have a three-layer structure (Examples 1, 2, 3, 4) or a two-layer structure. (Example-
5, θ) Both have a high 30% elongation elastic recovery rate of 90% or more, and a 30% elongation stress of 3 g/am//g/r
It can be seen that it is small, less than l. On the other hand, laminated nonwoven fabrics other than the present invention (Comparative Examples 1 and 2) using synthetic rubber nonwoven fabrics and synthetic fiber nonwoven fabrics with no elasticity and high elongation stress were
% elongation stress is high and elastic recovery rate is low. As a result, the texture of the laminated non-woven fabric was poor, and wrinkles appeared, probably due to structural cracks inside the non-woven fabric caused by the non-woven fabric being stretched and contracted.When used as a supporter, it felt like movement was restricted and lacked flexibility. Ta.
Claims (1)
織布において、伸縮性で低伸長応力の合成繊維系不織布
を用いた積層不織布。 2、第1請求項の合成ゴム系不織布が熱可塑性ポリウレ
タン系不織布であり、合成繊維系不織布が30%伸長応
力が2〜0.1g/cm//g/m^2、30%伸縮繰
り返し後の弾性回復率が80%以上の物性を有するポリ
オレフィン系不織布を用いた積層不織布。[Scope of Claims] 1. A laminated nonwoven fabric using a synthetic fiber nonwoven fabric that is stretchable and has low elongation stress in a nonwoven fabric that is a lamination of a synthetic rubber nonwoven fabric and a synthetic fiber nonwoven fabric. 2. The synthetic rubber nonwoven fabric of the first claim is a thermoplastic polyurethane nonwoven fabric, and the synthetic fiber nonwoven fabric has a 30% elongation stress of 2 to 0.1 g/cm//g/m^2 after repeated 30% expansion and contraction. A laminated nonwoven fabric using a polyolefin nonwoven fabric having a physical property of having an elastic recovery rate of 80% or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63297017A JP2577979B2 (en) | 1988-11-24 | 1988-11-24 | Laminated non-woven fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63297017A JP2577979B2 (en) | 1988-11-24 | 1988-11-24 | Laminated non-woven fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02143847A true JPH02143847A (en) | 1990-06-01 |
JP2577979B2 JP2577979B2 (en) | 1997-02-05 |
Family
ID=17841165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63297017A Expired - Fee Related JP2577979B2 (en) | 1988-11-24 | 1988-11-24 | Laminated non-woven fabric |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2577979B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007319561A (en) * | 2006-06-02 | 2007-12-13 | My Care:Kk | Affected part cover for bathing |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6017162A (en) * | 1983-07-01 | 1985-01-29 | 東レ株式会社 | Elastic nonwoven structure |
JPS6381887U (en) * | 1986-11-17 | 1988-05-30 |
-
1988
- 1988-11-24 JP JP63297017A patent/JP2577979B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6017162A (en) * | 1983-07-01 | 1985-01-29 | 東レ株式会社 | Elastic nonwoven structure |
JPS6381887U (en) * | 1986-11-17 | 1988-05-30 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007319561A (en) * | 2006-06-02 | 2007-12-13 | My Care:Kk | Affected part cover for bathing |
JP4636330B2 (en) * | 2006-06-02 | 2011-02-23 | 株式会社マイ・ケアー | Cover for affected area for bathing |
Also Published As
Publication number | Publication date |
---|---|
JP2577979B2 (en) | 1997-02-05 |
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