JPH04241159A - Thermally bonded nonwoven fabric - Google Patents
Thermally bonded nonwoven fabricInfo
- Publication number
- JPH04241159A JPH04241159A JP41882890A JP41882890A JPH04241159A JP H04241159 A JPH04241159 A JP H04241159A JP 41882890 A JP41882890 A JP 41882890A JP 41882890 A JP41882890 A JP 41882890A JP H04241159 A JPH04241159 A JP H04241159A
- Authority
- JP
- Japan
- Prior art keywords
- component
- nonwoven fabric
- weight
- ethylene
- fibers
- 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 36
- 238000002844 melting Methods 0.000 claims abstract description 18
- 230000008018 melting Effects 0.000 claims abstract description 18
- 229920001038 ethylene copolymer Polymers 0.000 claims abstract description 14
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 5
- 239000000835 fiber Substances 0.000 claims description 55
- 239000000853 adhesive Substances 0.000 claims description 23
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 21
- -1 acrylic ester Chemical class 0.000 claims description 19
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 5
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 3
- 239000011976 maleic acid Substances 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- 239000000463 material Substances 0.000 abstract description 4
- 239000000306 component Substances 0.000 description 41
- 239000002131 composite material Substances 0.000 description 23
- 229920000098 polyolefin Polymers 0.000 description 10
- 239000004743 Polypropylene Substances 0.000 description 9
- 229920001155 polypropylene Polymers 0.000 description 9
- 230000001070 adhesive effect Effects 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 229920002292 Nylon 6 Polymers 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000008358 core component Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000002074 melt spinning Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- 206010012735 Diarrhoea Diseases 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 238000010137 moulding (plastic) Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は熱接着不織布、殊に非ポ
リオレフィン系繊維素材との熱接着性に優れ、しかもポ
リエチレンの融点を超えない低温での熱接着され、スベ
リ摩擦抵抗が大きくゴム的な柔軟な感触を備えた熱接着
不織布に関するものである。[Industrial Application Field] The present invention is a heat-adhesive nonwoven fabric, which has excellent heat-adhesive properties, especially with non-polyolefin fiber materials, and can be thermally bonded at a low temperature that does not exceed the melting point of polyethylene. The present invention relates to a thermally bonded nonwoven fabric with a soft and flexible feel.
【0002】0002
【従来の技術】従来の熱接着不織布の多くはポリオレフ
ィン系の熱接着性繊維を含んで形成されている。そして
そのポリオレフィン系熱接着性繊維としては例えば特公
昭50−4767号公報や特公昭55−17807号公
報に記載されているようにポリプロピレンとポリエチレ
ン、またはポリプロピレンとエチレンの共重合体とを組
み合わせた複合繊維が基本的なものであった。BACKGROUND OF THE INVENTION Most conventional heat-adhesive nonwoven fabrics include polyolefin-based heat-adhesive fibers. The polyolefin-based heat-adhesive fiber is, for example, a composite made of a combination of polypropylene and polyethylene, or a copolymer of polypropylene and ethylene, as described in Japanese Patent Publication No. 50-4767 and Japanese Patent Publication No. 55-17807. Fibers were basic.
【0003】このようなポリオレフィン系の複合繊維は
比較的低温(120℃)で熱接着できること、及び得ら
れた不織布が他の不織布に比べて柔軟で風合がよいとい
う特徴がある。[0003] Such polyolefin composite fibers are characterized in that they can be thermally bonded at a relatively low temperature (120°C), and that the resulting nonwoven fabric is softer and has a better texture than other nonwoven fabrics.
【0004】0004
【発明が解決しようとする課題】しかしながらこれらポ
リオレフィン系の熱接着性繊維を用いた不織布はスベリ
摩擦抵抗が小さいため平滑な面に対して滑りやすく、例
えば各種のマットの下面の裏張りに用いた場合、僅かな
外力によっても移動して位置が変わるという不都合が生
じる。[Problems to be Solved by the Invention] However, these nonwoven fabrics using polyolefin-based heat-adhesive fibers have low sliding friction resistance, so they tend to slip easily on smooth surfaces, and are used, for example, as linings on the bottom of various mats. In this case, there is an inconvenience that even a slight external force causes the device to move and change its position.
【0005】また非晶質ポリエステルを熱接着成分とす
る複合繊維も試みられているが(特公昭63−4780
6号)ポリエステル系熱接着成分による不織布は柔軟性
にかけるため風合いがよくないという欠点があった。Composite fibers containing amorphous polyester as a thermal adhesive component have also been attempted (Japanese Patent Publication No. 4780/1983).
No. 6) Nonwoven fabrics made from polyester-based thermal adhesive components have the disadvantage of poor texture due to their flexibility.
【0006】本発明はポリオレフィンのもつ低い接着温
度と柔軟性を維持し、非ポリオレフィン系繊維にも接着
性のよい熱接着性複合繊維の熱融着によって形成された
熱接着不織布を提供するものである。The present invention provides a heat-adhesive nonwoven fabric formed by thermally fusing heat-adhesive conjugate fibers that maintains the low adhesion temperature and flexibility of polyolefins and has good adhesion to non-polyolefin fibers. be.
【0007】[0007]
【課題を解決するための手段】本発明者はエチレンカル
ボン酸のエステルとエチレンとの共重合体樹脂は、ポリ
オレフィン系樹脂と非ポリオレフィン系樹脂の双方に接
着性がよく、またスベリ摩擦抵抗大きく比較的低温で溶
融することを見いだし本発明に至った。[Means for Solving the Problems] The present inventors have discovered that a copolymer resin of ethylene carboxylic acid ester and ethylene has good adhesion to both polyolefin resins and non-polyolefin resins, and has a large sliding friction resistance. It was discovered that the material melts at a relatively low temperature, leading to the present invention.
【0008】すなわち本発明は、アクリル酸エステル及
び/又はメタアクリル酸エステルが5〜30重量%、ア
クリル酸、メタアクリル酸及びマレイン酸から選ばれた
エチレンカルボン酸が0〜10重量%でこれらの合計が
5〜30重量%のエチレンカルボン酸系モノマーと、エ
チレン95〜70重量%とからなるエチレン共重合体を
第1成分、融点(T℃)が130<T<270の熱可塑
性樹脂を第2成分として、第1成分が繊維表面の少なく
とも一部を占めてなる熱接着性複合繊維の熱融着によっ
て形成されていることを特徴としているものである。That is, the present invention comprises 5 to 30% by weight of acrylic ester and/or methacrylic ester and 0 to 10% by weight of ethylene carboxylic acid selected from acrylic acid, methacrylic acid and maleic acid. The first component is an ethylene copolymer consisting of a total of 5 to 30% by weight of an ethylene carboxylic acid monomer and 95 to 70% by weight of ethylene, and the second component is a thermoplastic resin with a melting point (T° C.) of 130<T<270. It is characterized in that it is formed by thermally fusing two components, the first component of which occupies at least a portion of the fiber surface, of thermoadhesive conjugate fibers.
【0009】上記複合繊維の熱接着成分となる第1成分
は、アクリル酸エステル、メタアクリル酸エステルなど
のエチレンカルボン酸エステルとエチレンとの共重合体
である。共重合体中のエチレンカルボン酸エステルの割
合は多いほど複合繊維の接着力が優れてくるが、30重
量%をこえると共重合体の硬度が低くなりゴム的性質が
つよくなる。このため複合繊維の表面が柔軟になってカ
ード通過性が悪くウェブを作りにくくなる。逆に5重量
%より少ないと接着力が不足するので、エチレンカルボ
ン酸エステルの共重合体中の割合は、5〜30重量%、
好ましくは10〜25重量%である。[0009] The first component serving as the thermal adhesive component of the composite fiber is a copolymer of ethylene and an ethylene carboxylic acid ester such as an acrylic ester or a methacrylic ester. The higher the proportion of ethylene carboxylic acid ester in the copolymer, the better the adhesion of the composite fiber will be, but if it exceeds 30% by weight, the copolymer will have lower hardness and stronger rubber properties. As a result, the surface of the composite fiber becomes soft, resulting in poor card passing properties and difficulty in forming a web. On the other hand, if it is less than 5% by weight, the adhesive strength will be insufficient, so the proportion of ethylene carboxylic acid ester in the copolymer should be 5 to 30% by weight,
Preferably it is 10 to 25% by weight.
【0010】エチレンカルボン酸エステルのアルコール
部は炭素数1〜5のものが好ましく、特にメチルアクリ
レート及びエチルアクリレートが好ましい。またエチレ
ン共重合体が上記エチレンとエチレンカルボン酸エステ
ルの他にさらに加えるモノマー分として、エチレンカル
ボン酸を加えた三元共重合体であれば、得られた複合繊
維の表面はゴム的性質が強くなり、これにより不織布は
一層柔軟なものになる。The alcohol moiety of the ethylene carboxylic acid ester preferably has 1 to 5 carbon atoms, with methyl acrylate and ethyl acrylate being particularly preferred. In addition, if the ethylene copolymer is a terpolymer with ethylene carboxylic acid added as a monomer in addition to the above-mentioned ethylene and ethylene carboxylic acid ester, the surface of the resulting composite fiber will have strong rubbery properties. This makes the nonwoven fabric even more flexible.
【0011】しかしエチレンカルボン酸は多すぎると溶
融紡糸時に繊維間の接着が起こるので、10%以下にす
る。このような三元共重合体の場合も、エチレンカルボ
ン酸エステルとエチレンカルボン酸の合計量は30重量
%以下にして、複合繊維のゴム的性質が過剰にならない
ようにする。 このような組成のエチレン共重合体の
融点はエチレンカルボン酸系のモノマーが多くなるほど
低融点になり、逆にエチレンの量が多くなるに従って高
融点になるが、その範囲は70〜130℃である。However, if the amount of ethylene carboxylic acid is too large, adhesion between fibers will occur during melt spinning, so the amount should be 10% or less. Even in the case of such a terpolymer, the total amount of ethylene carboxylic acid ester and ethylene carboxylic acid is kept at 30% by weight or less to prevent the rubbery properties of the composite fiber from becoming excessive. The melting point of an ethylene copolymer with such a composition becomes lower as the amount of ethylene carboxylic acid monomer increases, and conversely, as the amount of ethylene increases, the melting point becomes higher, but the range is 70 to 130 ° C. .
【0012】複合繊維の第2成分の融点は第1成分のエ
チレン共重合体の融点より高く、且つ第1成分の分解温
度より低くなければならない。第1成分の融点は130
℃以下、分解温度は300℃である。そこで第2成分の
融点(T℃)は300℃より低くなければならないが、
溶融紡糸の安定性からその範囲は130<T<270に
なる。このような融点をもつ熱可塑性樹脂は、ポリプロ
ピレン、ポリエチレンテレフタレート、ポリブチレンテ
レフタレート、ナイロン−6、ナイロン−66およびナ
イロン−12から選ばれる。又これらの共重合体も都合
よく用いられる。特にポリプロピレン、ポリエチレンテ
レフタレート、ナイロン−6は経済的理由から好ましく
使用できるので各々の樹脂の持つ柔軟性、弾性、吸湿性
等の特性を用途にあわせて適宜選択すれば良い。The melting point of the second component of the composite fiber must be higher than the melting point of the ethylene copolymer of the first component and lower than the decomposition temperature of the first component. The melting point of the first component is 130
℃ or less, the decomposition temperature is 300℃. Therefore, the melting point (T°C) of the second component must be lower than 300°C,
From the stability of melt spinning, the range is 130<T<270. Thermoplastic resins with such melting points are selected from polypropylene, polyethylene terephthalate, polybutylene terephthalate, nylon-6, nylon-66 and nylon-12. Copolymers of these are also conveniently used. In particular, polypropylene, polyethylene terephthalate, and nylon-6 are preferably used for economical reasons, so the properties of each resin such as flexibility, elasticity, and hygroscopicity may be appropriately selected depending on the intended use.
【0013】複合繊維の構造は、繊維表面の少なくとも
一部、好ましくは30%以上を第1成分が占めている構
造である。両成分の複合比は断面積比で第1成分/第2
成分が30/70〜70/30の範囲内にあることが、
複合繊維の紡糸性、強力、接着力の点から好ましい。The structure of the composite fiber is such that the first component occupies at least a portion, preferably 30% or more, of the fiber surface. The composite ratio of both components is the cross-sectional area ratio of the first component/second component.
The ingredients are within the range of 30/70 to 70/30,
It is preferable from the viewpoint of spinnability, strength, and adhesive strength of the composite fiber.
【0014】このような複合繊維を製造するには、第1
成分、第2成分共に紡糸温度におけるMFR(メルトフ
ロレート、JISK7210 に準じて測定する。加
重2169g)が15≦MFR<300になるように紡
糸温度を設定する。このような溶融流動性を示す第1成
分は、MI(メルトインデックス)が190℃、加重2
169gで測定するとき、5<MI<200となるもの
を用いる。紡糸温度は第2成分の融点を15℃以上高く
且つ300℃より低い温度である。紡糸後、20℃以上
で第1成分の融点より15℃低い温度以下で2倍以上延
伸すると良好な繊維強度が得られる。[0014] In order to produce such a composite fiber, the first step is to
The spinning temperature is set so that the MFR (melt fluorate, measured according to JIS K7210, weight: 2169 g) at the spinning temperature for both the component and the second component satisfies 15≦MFR<300. The first component exhibiting such melt fluidity has an MI (melt index) of 190°C and a weight of 2
When measuring at 169g, use one that satisfies 5<MI<200. The spinning temperature is 15°C or more higher than the melting point of the second component and lower than 300°C. After spinning, good fiber strength can be obtained by drawing the fiber twice or more at a temperature of 20° C. or higher and 15° C. lower than the melting point of the first component.
【0015】本発明に適用される複合繊維は高温下での
収縮が大きいものもあり(後述する実施例11では13
0℃ 乾熱収縮率40%)、このような繊維で実用上
収縮が邪魔になるときは80〜100℃(エチレン共重
合体の融点より低い温度で)緊張熱処理しておくとよい
。[0015] Some of the composite fibers applied to the present invention have large shrinkage at high temperatures (in Example 11 described later, 13
(40% dry heat shrinkage rate at 0°C).If shrinkage becomes a nuisance in practical use of such fibers, it is advisable to perform tension heat treatment at 80 to 100°C (at a temperature lower than the melting point of the ethylene copolymer).
【0016】また本発明に適用される複合繊維は比較的
低温で熱接着が可能であり、接着する繊維はポリオレフ
ィン系繊維は勿論、非ポリオレフィン系繊維でもよく接
着する。繊維以外でも各種プラスチックスの成型材、木
材、鉄にも接着可能であり、そのうえスベリ摩擦抵抗が
大きく柔軟性に富む。[0016] Furthermore, the composite fibers applied to the present invention can be thermally bonded at relatively low temperatures, and the fibers to be bonded can be not only polyolefin fibers but also non-polyolefin fibers. In addition to fibers, it can also be bonded to various plastic molding materials, wood, and iron, and it has high sliding friction resistance and is highly flexible.
【0017】また、第1成分のエチレン共重合体中のエ
チレンカルボン酸エステルの含有量は30重量%まで増
加しても紡糸可能であり、このため得られる複合繊維の
熱接着力を大幅に向上させることができる。Furthermore, even if the content of ethylene carboxylic acid ester in the first component ethylene copolymer is increased to 30% by weight, it can be spun, which greatly improves the thermal adhesive strength of the resulting composite fiber. can be done.
【0018】[0018]
【実施例】[実施例1〜11]第1成分としてエチレン
共重合体、第2成分としてポリプロピレン(PP)、ポ
リエチレンテレフタレート(PET)、ポリブチレンテ
レフタレート(PBT)、ナイロン−6(Ny−6)、
ナイロン−66(Ny−66)及びエチレンプロピレン
ランダム共重合体(EP)を使い複合比を、第1成分4
0:第2成分60 の割合で、鞘芯型(S/C)及び
並列型(S/S)の複合繊維を紡糸した。次いでこれを
二つに分け、その一つを60℃の温水中で延伸糸、スタ
ッファボックスで機捲縮を付与し、乾燥後切断して繊維
長51mmのステープル繊維とした。また、他の一つを
60℃の温水中で延伸し、直ちに切断して繊維長5mm
の短カット繊維とした。[Examples] [Examples 1 to 11] Ethylene copolymer as the first component, polypropylene (PP), polyethylene terephthalate (PET), polybutylene terephthalate (PBT), nylon-6 (Ny-6) as the second component ,
Using nylon-66 (Ny-66) and ethylene propylene random copolymer (EP), the composite ratio was adjusted to 4 for the first component.
Sheath-core type (S/C) and parallel type (S/S) composite fibers were spun at a ratio of 0:60 of the second component. Next, this was divided into two parts, one of which was drawn in hot water at 60°C, crimped using a stuffer box, dried, and then cut to obtain staple fibers with a fiber length of 51 mm. In addition, the other one was stretched in hot water at 60°C and immediately cut to a fiber length of 5 mm.
It was made into short cut fibers.
【0019】また、比較のためエチレン酢酸ビニル共重
合体を鞘成分に、ポリプロピレンを芯成分にした鞘芯型
複合繊維を同様にして製造した。鞘成分の酢酸ビニルの
共重合体に占める割合は6%であった。次に、上記繊維
を用いて不織布及び紙を得た。不織布は本発明のステー
プル繊維30%と2デニール、51mmのポリエステル
繊維を混綿し、ローラカードでウエブとした後120℃
熱風貫通型熱加工機でウエブをネットに挟んで処理し、
複合繊維の熱接着成分を溶融させ、繊維間を接着し、目
付40g/m2の不織布となした。For comparison, a sheath-core type composite fiber was produced in the same manner using ethylene vinyl acetate copolymer as the sheath component and polypropylene as the core component. The proportion of vinyl acetate as a sheath component in the copolymer was 6%. Next, nonwoven fabric and paper were obtained using the above fibers. The non-woven fabric is a blend of 30% staple fiber of the present invention and 2 denier, 51 mm polyester fiber, made into a web using a roller card, and then heated at 120°C.
Process the web by sandwiching it between nets using a hot air penetrating type thermal processing machine.
The thermal adhesive component of the composite fibers was melted and the fibers were bonded together to form a nonwoven fabric with a basis weight of 40 g/m2.
【0020】また紙は、上記熱接着性繊維を5mmに切
断し、この短カット繊維20%と太さ2デニール、長さ
5mmのレーヨンとを混合して抄造し、120℃で乾燥
して坪量20g/m2の紙となした。Paper is made by cutting the above heat-adhesive fibers into 5 mm pieces, mixing 20% of the short cut fibers with rayon having a thickness of 2 deniers and a length of 5 mm, and drying the paper at 120° C. The paper weight was 20 g/m2.
【0021】上記実施例、比較例の各繊維の諸性能を表
1に示し、不織布及び紙の裂断長(km)を表2及び表
3に示す。Table 1 shows the various performances of each fiber of the above examples and comparative examples, and Tables 2 and 3 show the tearing lengths (km) of the nonwoven fabric and paper.
【0022】[0022]
【表1】[Table 1]
【0023】[0023]
【表2】[Table 2]
【0024】[0024]
【表3】[Table 3]
【0025】なお上記不織布と紙の裂断長は、幅50m
m、長さ100mmの試料を、引張速度300m/分で
破断強力を測定し、次の式によって計算した。また風合
は感触により比較例より柔らかいものを○にした。[0025] The tearing length of the above-mentioned nonwoven fabric and paper is 50 m in width.
The breaking strength of a sample with a length of 100 mm and a tensile speed of 300 m/min was measured and calculated using the following formula. Regarding the texture, those that were softer than the comparative example were rated ○.
【0026】[0026]
【式1】[Formula 1]
【0027】[実施例12〜15、比較例2〜4]第1
成分としてエチレン共重合体、第2成分として270℃
におけるMFRが13g/10分の熱減性タイプのポリ
プロピレンを用い、第1成分55、第2成分45の重量
割合で鞘/芯型(S/C)複合繊維を紡糸した。次いで
これを60℃の温水中で延伸し実施例1と同様にして2
.3デニール×51mmのステープル繊維とした。[Examples 12 to 15, Comparative Examples 2 to 4] First
Ethylene copolymer as a component, 270°C as a second component
A sheath/core type (S/C) composite fiber was spun using heat-reducible polypropylene having an MFR of 13 g/10 min at a weight ratio of 55 for the first component and 45 for the second component. Next, this was stretched in hot water at 60°C, and the same procedure as in Example 1 was carried out to obtain 2.
.. It was made into a staple fiber of 3 denier x 51 mm.
【0028】比較例としてポリエチレンテレフタレート
を芯成分とし高密度ポリエチレンを鞘成分とした2デニ
ール×51mmおよび4デニール×5mm[NBF(S
H)、大和紡績(株)製]、ポリプロピレンを芯成分と
し高密度ポリエチレンを鞘成分とした2デニール×51
mm[NBF(H)大和紡績(株)製]をそれぞれロー
ラーカードでウェブとしたのち熱風貫通型熱加工機でウ
ェブをネットに挟んで処理し、複合繊維の熱接着成分を
溶融させて繊維間を接着し、目付40g/m2の熱接着
不織布とした。上記実施例12〜15と比較例2〜4の
評価結果を表4に示した。As comparative examples, 2 denier x 51 mm and 4 denier x 5 mm [NBF (S
H), manufactured by Daiwabo Co., Ltd.], 2 denier x 51 with polypropylene as the core component and high-density polyethylene as the sheath component
mm [NBF (H) manufactured by Daiwabo Co., Ltd.] was made into a web using a roller card, and then processed by sandwiching the web between nets using a hot air penetration type thermal processing machine to melt the thermal adhesive component of the composite fiber and create a bond between the fibers. were adhered to form a heat-adhesive nonwoven fabric with a basis weight of 40 g/m2. The evaluation results of Examples 12 to 15 and Comparative Examples 2 to 4 are shown in Table 4.
【0029】[0029]
【表4】[Table 4]
【0030】不織布の風合は比較例2および3の同一デ
ニールの不織布より柔らかいものを○にした。また不織
布の滑り摩擦抵抗は次のようにして測定した。Regarding the feel of the nonwoven fabric, those that were softer than the nonwoven fabrics of Comparative Examples 2 and 3 of the same denier were rated ○. In addition, the sliding friction resistance of the nonwoven fabric was measured as follows.
【0031】鏡面仕上げの板ガラス上に10cm角の不
織布をのせ、その中心部に13gの5cm×5cmのア
ルミ板をのせ、その上に1個が50g、100g、およ
び200gの分銅をそれぞれの測定条件に応じてのせ、
アルミ板の長さ方向の不織布端にクリップを装着してク
リップをハンドタイプのバネ秤で緩やかに引っ張り、平
衡した引っ張り張力をg単位で測定し評価した。A 10 cm square piece of non-woven fabric is placed on a mirror-finished plate glass, a 13 g 5 cm x 5 cm aluminum plate is placed in the center of the non-woven fabric, and weights each weighing 50 g, 100 g, and 200 g are placed on top of the non-woven fabric under the respective measurement conditions. Place according to the
A clip was attached to the end of the nonwoven fabric in the longitudinal direction of the aluminum plate, the clip was gently pulled using a hand-type spring balance, and the balanced tensile tension was measured in g for evaluation.
【0032】実施例12〜15の不織布は従来の不織布
に比べて著しく滑りにくかった。The nonwoven fabrics of Examples 12 to 15 were significantly less slippery than conventional nonwoven fabrics.
【0033】[0033]
【発明の効果】このように本発明の熱接着不織布は、ア
クリル酸エステル及び/又はメタアクリル酸エステルが
5〜30重量%、アクリル酸、メタアクリル酸及びマレ
イン酸から選ばれたエチレンカルボン酸が0〜10重量
%でこれらの合計が5〜30重量%のエチレンカルボン
酸系モノマーと、エチレン95〜70重量%とからなる
エチレン共重合体を第1成分、融点(T℃)が130<
T<270の熱可塑性樹脂を第2成分とし、その第1成
分が繊維表面の少なくとも一部を占めてなる熱接着性複
合繊維が10重量%以上含まれてこの第1成分の熱溶融
により接合されてなるものであり、殊に上記エチレン共
重合体は手で触ると極めて柔らかく感じ、従来のポリオ
レフィン系の熱接着性繊維よりも太繊度であってもソフ
トな風合を感じる。Effects of the Invention As described above, the heat-adhesive nonwoven fabric of the present invention contains 5 to 30% by weight of acrylic ester and/or methacrylic ester and ethylene carboxylic acid selected from acrylic acid, methacrylic acid, and maleic acid. The first component is an ethylene copolymer consisting of an ethylene carboxylic acid monomer of 0 to 10% by weight and a total of 5 to 30% by weight, and 95 to 70% by weight of ethylene, and the melting point (T ° C.) is 130<
The second component is a thermoplastic resin with T<270, and the first component contains 10% by weight or more of thermally bondable composite fibers that occupy at least a portion of the fiber surface, and is bonded by thermal melting of the first component. In particular, the above-mentioned ethylene copolymer feels extremely soft to the touch, and even when the fiber is thicker than conventional polyolefin heat-adhesive fibers, it feels soft to the touch.
【0034】したがってナプキンや紙オムツの表面材シ
ートとして好適となり、特に軟便用の紙オムツの表面材
として有益となる。[0034] Therefore, it is suitable as a surface material sheet for napkins and paper diapers, and is particularly useful as a surface material for paper diapers for soft stools.
【0035】さらにスベリにくい特徴を有するから、玄
関マット、カーペット、バスマット等の敷物の裏張り用
として、あるいは各種置物の下敷きや下張り用として好
都合となる。そしてこのような用途に適用する際には、
上記したエチレン共重合体を第1成分とした熱接着性複
合繊維が床面側に集中して存在した不織布を形成すると
よい。そのうえ熱接着温度が比較的低いからヘアードラ
イヤーやハンダゴテ等の熱源を利用して不織布を他の物
品に接着することができるなど取り扱い上至便である。Furthermore, since it has a non-slip characteristic, it is suitable for use as a backing for rugs such as entrance mats, carpets, bath mats, etc., or as underlays and underlays for various ornaments. When applied to such uses,
It is preferable to form a nonwoven fabric in which heat-adhesive conjugate fibers containing the above-mentioned ethylene copolymer as a first component are concentrated on the floor surface side. Furthermore, since the thermal bonding temperature is relatively low, the nonwoven fabric can be bonded to other articles using a heat source such as a hair dryer or a soldering iron, making it convenient to handle.
Claims (1)
クリル酸エステルが5〜30重量%、アクリル酸、メタ
アクリル酸及びマレイン酸から選ばれたエチレンカルボ
ン酸が0〜10重量%でこれらの合計が5〜30重量%
のエチレンカルボン酸系モノマーと、エチレン95〜7
0重量%とからなるエチレン共重合体を第1成分、融点
(T℃)が130<T<270の熱可塑性樹脂を第2成
分とし、その第1成分が繊維表面の少なくとも一部を占
めてなる熱接着性複合繊維が10重量%以上含まれてこ
の第1成分の熱溶融により接合されている熱接着不織布
。Claim 1: 5 to 30% by weight of acrylic ester and/or methacrylic ester, 0 to 10% by weight of ethylene carboxylic acid selected from acrylic acid, methacrylic acid, and maleic acid, and the total amount of these is 5 to 30% by weight. ~30% by weight
of ethylene carboxylic acid monomer and ethylene 95-7
The first component is an ethylene copolymer consisting of 0% by weight, the second component is a thermoplastic resin with a melting point (T ° C.) of 130 A heat-adhesive nonwoven fabric containing 10% by weight or more of heat-adhesive conjugate fibers and bonded by thermal melting of the first component.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2418828A JP2571155B2 (en) | 1990-12-27 | 1990-12-27 | Heat bonded nonwoven |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2418828A JP2571155B2 (en) | 1990-12-27 | 1990-12-27 | Heat bonded nonwoven |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04241159A true JPH04241159A (en) | 1992-08-28 |
JP2571155B2 JP2571155B2 (en) | 1997-01-16 |
Family
ID=18526596
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2418828A Expired - Fee Related JP2571155B2 (en) | 1990-12-27 | 1990-12-27 | Heat bonded nonwoven |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2571155B2 (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01280020A (en) * | 1988-04-28 | 1989-11-10 | Teijin Ltd | Thermally bondable conjugated yarn |
JPH03287875A (en) * | 1990-04-04 | 1991-12-18 | Chisso Corp | Heat-weldable conjugate fiber and production thereof |
JPH04214411A (en) * | 1990-03-26 | 1992-08-05 | Daiwabo Create Kk | Hot-melt conjugated fiber and nonwoven fabric |
-
1990
- 1990-12-27 JP JP2418828A patent/JP2571155B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01280020A (en) * | 1988-04-28 | 1989-11-10 | Teijin Ltd | Thermally bondable conjugated yarn |
JPH04214411A (en) * | 1990-03-26 | 1992-08-05 | Daiwabo Create Kk | Hot-melt conjugated fiber and nonwoven fabric |
JPH03287875A (en) * | 1990-04-04 | 1991-12-18 | Chisso Corp | Heat-weldable conjugate fiber and production thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2571155B2 (en) | 1997-01-16 |
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