JPH0418121A - Hot-melt fiber - Google Patents
Hot-melt fiberInfo
- Publication number
- JPH0418121A JPH0418121A JP11666190A JP11666190A JPH0418121A JP H0418121 A JPH0418121 A JP H0418121A JP 11666190 A JP11666190 A JP 11666190A JP 11666190 A JP11666190 A JP 11666190A JP H0418121 A JPH0418121 A JP H0418121A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- propylene
- resin
- nonwoven fabric
- butene
- 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
- 239000000835 fiber Substances 0.000 title claims abstract description 57
- 239000012943 hotmelt Substances 0.000 title abstract 2
- 229920005989 resin Polymers 0.000 claims abstract description 29
- 239000011347 resin Substances 0.000 claims abstract description 29
- VXNZUUAINFGPBY-UHFFFAOYSA-N ethyl ethylene Natural products CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 25
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 21
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 21
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 9
- 239000004700 high-density polyethylene Substances 0.000 claims abstract description 6
- 229920001903 high density polyethylene Polymers 0.000 claims abstract description 5
- 239000002131 composite material Substances 0.000 claims description 16
- -1 polypropylene Polymers 0.000 claims description 9
- 239000004743 Polypropylene Substances 0.000 claims description 7
- 229920001155 polypropylene Polymers 0.000 claims description 7
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 6
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 3
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 3
- 229920001748 polybutylene Polymers 0.000 claims description 2
- 239000004745 nonwoven fabric Substances 0.000 abstract description 49
- 239000000306 component Substances 0.000 abstract description 13
- 239000008358 core component Substances 0.000 abstract description 3
- 230000000704 physical effect Effects 0.000 abstract description 3
- 229920001684 low density polyethylene Polymers 0.000 abstract description 2
- 239000004702 low-density polyethylene Substances 0.000 abstract description 2
- 229940099514 low-density polyethylene Drugs 0.000 abstract 1
- 238000012545 processing Methods 0.000 description 11
- 229920005606 polypropylene copolymer Polymers 0.000 description 10
- 239000002994 raw material Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 7
- 238000009987 spinning Methods 0.000 description 7
- 238000004049 embossing Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920004889 linear high-density polyethylene Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
【発明の詳細な説明】
[!業上の利用分野〕
本発明は熱融着性繊維に関する。更に詳しくは、不織布
加工性ならびに不織布物性の優れた熱融着性繊維に関す
る。[Detailed description of the invention] [! Field of Industrial Application] The present invention relates to heat-fusible fibers. More specifically, the present invention relates to heat-fusible fibers with excellent nonwoven processability and nonwoven physical properties.
[従来の技術とその問題点コ
熱融着性繊維を用いた不織布は、接着剤等の化学的なバ
インダーを使用していないため安全性が高く、また不織
布の嵩高性および用合いが良いことから、紙オムツ、ナ
プキン等の使い捨て衛剤用品の表皮剤として広く使用さ
れている。[Conventional technology and its problems] Nonwoven fabrics using heat-fusible fibers are highly safe because they do not use chemical binders such as adhesives, and the bulkiness of nonwoven fabrics makes them easy to use. It is widely used as a skin agent for disposable hygiene products such as disposable diapers and napkins.
熱融着性繊維はそのl!IN構造から、複合繊維と単一
構造の繊維とに分けられる。Heat-fusible fibers are the best! Based on the IN structure, fibers can be divided into composite fibers and single-structure fibers.
そして該複合MINとしては、低融点樹脂と高融点樹脂
の2成分からなり、2成分の樹脂を並列に配した並列型
および高融点樹脂を芯にし低融点樹脂を鞘に配した芯鞘
型の構造が提案されている。The composite MIN consists of two components, a low melting point resin and a high melting point resin, and includes a parallel type in which the two component resins are arranged in parallel, and a core-sheath type in which the high melting point resin is the core and the low melting point resin is in the sheath. structure is proposed.
低融点樹脂としてはポリエチレンが、高融点樹脂として
はポリプロピレン、ポリエステルが多く用いられている
。Polyethylene is often used as a low melting point resin, and polypropylene and polyester are often used as high melting point resins.
この複合繊維の特徴は、ウェブの固定を低融点樹脂が行
なうことであり、これにより′柔軟で嵩高な不織布が製
造可能である。A feature of this composite fiber is that the web is fixed by a low-melting point resin, which makes it possible to produce a flexible and bulky nonwoven fabric.
単一成分の繊維としては、ポリプロピレン、ポリエチレ
ン繊維が主流である。この繊維は不織布の嵩高性、柔軟
性で複合繊維に劣るが低価格のため広く利用されている
。As single component fibers, polypropylene and polyethylene fibers are mainstream. Although this fiber is inferior to composite fibers in bulk and flexibility of nonwoven fabrics, it is widely used because of its low price.
しかし、上記公知の熱融着性繊維には以下の問題点が見
られる。However, the above known heat-fusible fibers have the following problems.
熱融着性繊維は、熱エンボスロール法およびサクション
ドライヤー等を用いた熱風法により不織布に製造される
。どちらの製造方法においても、不織布の加工温度が高
いと不織布強力は高くなるが不織布の風合いが悪く、ま
た不織布加工温度が低いと不織布強力が低くなり、不織
布加工温度を厳密に管理しなければならないという問題
が見られた。The heat-fusible fiber is manufactured into a nonwoven fabric by a hot embossing roll method and a hot air method using a suction dryer or the like. In both manufacturing methods, if the nonwoven fabric processing temperature is high, the nonwoven fabric strength will be high, but the texture of the nonwoven fabric will be poor, and if the nonwoven fabric processing temperature is low, the nonwoven fabric strength will be low, so the nonwoven fabric processing temperature must be strictly controlled. This problem was found.
この問題点の解決策として、複合繊維、単一成分*I!
共に不織布の低温加工性を改善するために融点の低い樹
脂を用いた繊維が提案されているが、この場合、不織布
の低温加工は可能となるが不織布強力は高くなく十分な
効果は得られてない。As a solution to this problem, composite fibers, single component *I!
In order to improve the low-temperature processability of non-woven fabrics, fibers using resins with a low melting point have been proposed, but in this case, low-temperature processing of non-woven fabrics is possible, but the strength of the non-woven fabric is not high and sufficient effects cannot be obtained. do not have.
このような従来の技術の問題点を解決するために、本発
明者等は不織布製造において不織布加工温度幅が広く且
つ不織布強力の高い不織布が製造可能な熱融着性繊維を
鋭意研究した結果、樹脂成分としてポリオレフィン樹脂
に特定組成のプロピレンとブテン−1の共重合体を一定
範囲内の比率で混合した樹脂組成物を用いて繊維を製造
すると上記の技術問題が解決できることを知見して本発
明を完成した。In order to solve the problems of the conventional technology, the present inventors conducted extensive research on heat-fusible fibers that can be processed in a wide range of non-woven fabric processing temperatures and can produce non-woven fabrics with high strength. The present invention was based on the finding that the above technical problem can be solved by producing fibers using a resin composition in which a polyolefin resin is mixed with a copolymer of propylene and butene-1 having a specific composition at a ratio within a certain range. completed.
[訝題を解決するための手段] 本発明は下記(1)または(2)の構成を有する。[Means to solve the question] The present invention has the following configuration (1) or (2).
(1)ポリオレフィン樹脂100重量部に対し、プロピ
レン含有量が55〜85モル%のプロピレンとブテン−
1の共重合体を5〜100重量部添加した樹脂からなる
熱融着性繊維。(1) Propylene and butene with a propylene content of 55 to 85 mol% based on 100 parts by weight of polyolefin resin.
A heat-fusible fiber made of a resin to which 5 to 100 parts by weight of copolymer No. 1 is added.
(2)高密度若しくは直鎖状低密度ポリエチレン樹脂、
ポリプロピレン樹脂若しくはポリブテン−1樹脂から選
ばれたいづれか一以上の樹脂からなる繊維を複合繊維の
一方の成分Aとし、ポリオレフィン樹脂100重量部に
対し、プロピレン含有量が55〜85モル%のプロピレ
ンとブテン−1の共重合体を5〜100重量部添加した
樹脂からなる繊維を複合繊維の他方の成分Bとしてなり
、前記B成分の全部若しくは一部が該複合繊維の表面を
構成してなる熱融着性複合繊維。(2) High-density or linear low-density polyethylene resin,
One component A of the composite fiber is a fiber made of one or more resins selected from polypropylene resin or polybutene-1 resin, and propylene and butene with a propylene content of 55 to 85 mol% based on 100 parts by weight of polyolefin resin. The other component B of the composite fiber is a fiber made of a resin to which 5 to 100 parts by weight of the copolymer of -1 is added, and all or part of the component B constitutes the surface of the composite fiber. Adhesive composite fiber.
本発明で用いられるポリオレフィン樹脂は、低密度ポリ
エチレン、直鎖状低密度ポリエチレン、高密度ポリエチ
レンもしくは結晶性ポリプロピレン、プロピレンと少量
のエチレンなどのα−オレフィンとの共重合体あるいは
これらの混合物が挙げられる。The polyolefin resin used in the present invention includes low density polyethylene, linear low density polyethylene, high density polyethylene or crystalline polypropylene, a copolymer of propylene and a small amount of α-olefin such as ethylene, or a mixture thereof. .
本発明で用いられるプロピレンが含有量が55〜85モ
ル%のプロピレンとブテン−1の共重合体は、例えば特
公昭54−48845に記載の方法により製造すること
ができる。The copolymer of propylene and butene-1 having a propylene content of 55 to 85 mol % used in the present invention can be produced, for example, by the method described in Japanese Patent Publication No. 54-48845.
本発明で用いられるプロピレンとブテン−1の共2 重
合体は、プロピレン含有量が55〜85モル%でなけれ
ばならない、プロピレン含有量が55モル%未満では繊
維の安定生産性が低下し、また85モル%を超えると十
分な効果が得られない。The copolymer of propylene and butene-1 used in the present invention must have a propylene content of 55 to 85 mol%. If the propylene content is less than 55 mol%, the stable productivity of fibers will decrease, and If it exceeds 85 mol%, sufficient effects cannot be obtained.
本発明で用いられるプロピレンとブテン−1の共重合体
の配合量は、前記ポリオレフィン樹脂100重量部に対
して5〜100重量部、好ましくは10〜70重量部で
ある。The amount of the copolymer of propylene and butene-1 used in the present invention is 5 to 100 parts by weight, preferably 10 to 70 parts by weight, based on 100 parts by weight of the polyolefin resin.
配合量が5重量部未満では十分な効果が得られず、また
100重量部を超えると安定した繊維の製造ができな
くなる。If the amount is less than 5 parts by weight, a sufficient effect will not be obtained, and if it exceeds 100 parts by weight, stable production of fibers will not be possible.
本発明の熱融着性繊維には光安定剤、造核剤、滑剤、帯
電防止剤、顔料、過酸化物のごときラジカル発生剤、金
属石鹸等の分散剤もしくは中和剤を本発明の目的を損な
わない範囲で併用することができる。The heat-fusible fibers of the present invention contain light stabilizers, nucleating agents, lubricants, antistatic agents, pigments, radical generators such as peroxides, and dispersants or neutralizing agents such as metal soaps for the purpose of the present invention. They can be used together as long as they do not impair the properties.
本発明の熱融着性繊維に使用する原料樹脂は、前記ポリ
オレフィンにプロピレンとブテン−1の共重合体ならび
に上述の各種化合物の所定量を通常の混合装置例えばヘ
ンセルミキサー(商品名)、スーパーミキサー、リボン
ブレンダー、バンバリーミキサ−などを用いて混合し、
通常の単軸押出機、2軸押用機、ブラベンダー又はロー
ルなどで溶融混練温度150〜300℃、好ましくは1
80℃〜250℃で溶融混練ペレタイズすることにより
得ることができる。The raw material resin used for the heat-fusible fiber of the present invention is prepared by mixing the polyolefin, a copolymer of propylene and butene-1, and predetermined amounts of the various compounds described above using a conventional mixing device such as a Hensel mixer (trade name), a super Mix using a mixer, ribbon blender, Banbury mixer, etc.
Melt-kneading temperature 150-300℃, preferably 1
It can be obtained by melt-kneading and pelletizing at 80°C to 250°C.
本発明の熱融着性繊維は、上記の原料を単独にまたは並
列型複合繊維の1成分の原料としてもしくは芯鞘型複合
繊維の好ましくは鞘成分の原料として用い、通常公知の
溶融紡糸法にて紡糸した後延伸、捲縮処理して製造で鮒
る。The heat-fusible fiber of the present invention can be produced by using the above-mentioned raw materials alone or as a raw material for one component of a parallel type conjugate fiber, or preferably as a raw material for a sheath component of a core-sheath type conjugate fiber, using a commonly known melt spinning method. After spinning, it is stretched and crimped before being manufactured.
該複合繊維の好ましくは芯成分として使用できる原料樹
脂は、前記(2)の成分Aとして例示される高密度ポリ
エチレン樹脂等に限られず、公知の溶融紡糸可能な原料
樹脂例えば、ポリエーテル、ポリエステル、ポリエステ
ルエーテル若しくはポリアミド等を使用することができ
る。The raw material resin that can preferably be used as the core component of the composite fiber is not limited to the high-density polyethylene resin exemplified as component A in (2) above, but may also include known melt-spun raw material resins such as polyether, polyester, Polyester ether or polyamide can be used.
[実施例]
以下実施例および比較例に基付いて本発明を具体的に説
明するが、本発明はこれらに限定されるものではない、
尚実施例中に示された物性値の測定法または定義をまと
めて示しておく。[Examples] The present invention will be specifically explained below based on Examples and Comparative Examples, but the present invention is not limited thereto.
The measurement methods or definitions of the physical property values shown in the Examples will be summarized below.
MFR(メルトフローレイト): ^S丁M 01238の条件(L)による。MFR (melt flow rate): ^ According to condition (L) of S-cho M 01238.
Ml(メルトインデックス): ^STM 01238の条件(E)による。Ml (melt index): ^ According to condition (E) of STM 01238.
不織布強カニ
目付は重量的20g/■2の不織布より、機械方向に長
さ10c諺、幅5c園および長さ5cm、幅10c層の
試験片を切り出し該試験片を用いて、引張試験機を用い
て引張速度100mm/■in、試験片つかみ間隔5c
−の条件で、不織布の機械方向(MO)と機械方向と垂
直方向(CD)の破断強力を測定し、不織布の目付け2
0g当たりに換算して表した。Non-woven fabric strong fabric weight is determined by cutting out a test piece with a length of 10 cm and a width of 5 cm in the machine direction, and a length of 5 cm and a width of 10 cm from a non-woven fabric with a weight of 20 g/2. The tensile speed was 100mm/inch, and the specimen gripping interval was 5c.
- The breaking strength of the nonwoven fabric in the machine direction (MO) and machine direction and perpendicular direction (CD) was measured under the conditions of
Expressed in terms of 0g.
実施例1〜4
高密度ポリエチレン(M I −16)100重量部に
対して、 BIT 0.1重量部、ステアリン酸カルシ
ュウム 0.1重量部およびプロピレン含有量74モル
%、MFR14のプロピレンとブテン−1共重合体を表
1に示す割合でヘンセルミキサーに入れ、3分間攪拌混
合した後、口径40mmの単軸押出機で200℃にて造
粒し原料ペレットを得た。Examples 1 to 4 Based on 100 parts by weight of high-density polyethylene (MI-16), 0.1 part by weight of BIT, 0.1 part by weight of calcium stearate, 74 mol% propylene content, propylene and butene with MFR 14. 1 copolymer was put into a Hensel mixer in the ratio shown in Table 1, stirred and mixed for 3 minutes, and then granulated at 200° C. with a single-screw extruder having a diameter of 40 mm to obtain raw material pellets.
ノズル径0.5mm 、ノズル数450個を有する芯鞘
型複合繊維紡糸機により、芯成分樹脂にポリプロピレン
(MFRIO)を、鞘成分樹脂として前記原料を用い、
紡糸温度280℃、紡糸速度800■/sinの条件で
9デニールの芯鞘型複合未延伸糸を得た。Using a core-sheath type composite fiber spinning machine with a nozzle diameter of 0.5 mm and a number of nozzles of 450, polypropylene (MFRIO) is used as the core component resin and the above raw material is used as the sheath component resin,
A core-sheath type composite undrawn yarn of 9 denier was obtained under the conditions of a spinning temperature of 280° C. and a spinning speed of 800 μ/sin.
次にこの未延伸糸をステーブルファイバー製造設備を用
いて、延伸温度100℃、延伸倍率3倍の条件で延伸し
、捲縮を与えた後カットし3デニール長さ50m■のス
テーブルファイバーを得た。Next, this undrawn yarn was stretched using stable fiber manufacturing equipment at a stretching temperature of 100°C and a stretching ratio of 3 times, crimped, and then cut to produce a stable fiber with a length of 3 denier and 50 m. Obtained.
このステーブルファイバーを巻き取り速度7.5m/w
inのカード機によりウェブとした後、加熱エンボスロ
ールによりエンボス点面積7%、線圧11kg/c■2
、ロール速度3諷/■inの条件でウェブをポイントボ
ンディングし不織布とした。Winding speed of this stable fiber is 7.5m/w
After forming into a web using an in-line card machine, the embossing point area is 7% and the linear pressure is 11 kg/c■2 using a heated embossing roll.
The web was point-bonded to obtain a nonwoven fabric at a roll speed of 3 mm/inch.
表1に不織布強力の結果を示した。Table 1 shows the results of the strength of the nonwoven fabric.
いずれも広い温度範囲で優れた不織布強力を持りた不織
布が得られた。また、不織布の風合いを手触りにより検
査したが何れの不織布も柔軟であった。In all cases, nonwoven fabrics with excellent nonwoven fabric strength over a wide temperature range were obtained. In addition, the texture of the nonwoven fabrics was examined by touch, and all nonwoven fabrics were found to be flexible.
比較例1〜3
プロピレン含量75モル%、MFR14のプロピレンと
ブテン−1の共重合体の添加量を0.4.105重量部
とした以外は実施例1〜3と同様に実施した。Comparative Examples 1 to 3 Examples 1 to 3 were carried out in the same manner as in Examples 1 to 3, except that the amount of the copolymer of propylene and butene-1 having a propylene content of 75 mol% and an MFR of 14 was 0.4.105 parts by weight.
表1に不織布強力の結果を示した。比較例1.2は、エ
ンボスロール温度が低いと不織布強力が弱くなり、実施
例1〜3に比べ不織布加工温度が狭いことが判る。比較
例3は、糸切れが多く可紡性不良のため繊維が得られな
かった。Table 1 shows the results of the strength of the nonwoven fabric. It can be seen that in Comparative Example 1.2, when the embossing roll temperature is low, the strength of the nonwoven fabric becomes weaker, and the processing temperature of the nonwoven fabric is narrower than in Examples 1 to 3. In Comparative Example 3, fibers could not be obtained due to many yarn breakages and poor spinnability.
実施例5〜6
プロピレンブテン−1の共重合体の添加量を50重量部
とし、この共重合体のプロピレン含有量が表2に示され
るプロピレンとブテン−1の共重合体を用いた以外は実
施例1〜3と同様に実施した。Examples 5 to 6 Except for using a copolymer of propylene and butene-1 in which the amount of propylene-butene-1 copolymer added was 50 parts by weight, and the propylene content of this copolymer was shown in Table 2. It was carried out in the same manner as Examples 1-3.
表2に不織布強力の結果を示す、いずれも広い温度範囲
で優れた不織布強力を持りた不織布が得られた。また、
不織布の風合いを手触りにより検査したが何れの不織布
も柔軟であった。The results of the nonwoven fabric strength are shown in Table 2. In all cases, nonwoven fabrics with excellent nonwoven fabric strength over a wide temperature range were obtained. Also,
The texture of the nonwoven fabrics was examined by touch, and all nonwoven fabrics were found to be flexible.
比較例4〜5
プロピレン含有量が50モル%および90モル%のプロ
ピレンとブテン−1共重合体を用いた以外は実施例4〜
5と同様に実施した。Comparative Examples 4 to 5 Examples 4 to 5 except that propylene and butene-1 copolymers with propylene contents of 50 mol% and 90 mol% were used.
It was carried out in the same manner as in 5.
表2に不織布強力の結果を示す。Table 2 shows the results of the strength of the nonwoven fabric.
比較例4は、延伸工程でトウが延伸ロールに壱ぎ付か繊
維が得られなかフた。比較例5は、実施例4〜5と比べ
不織布加工温度幅が狭くまた不織布強力も低いことが判
る。In Comparative Example 4, the tow stuck to the drawing roll during the drawing process and no fibers were obtained. It can be seen that Comparative Example 5 has a narrower nonwoven fabric processing temperature range and lower nonwoven fabric strength than Examples 4 and 5.
実施例6および比較例6
MFRIGのポリプロピレン100重量部に対して、B
IT 0.1重量部、ステアリン酸カルシュウム0.1
重量部およびプロピレン含有量74モル%、MFR14
のプロピレンとブテン〜1の共重合体を表3に示す割合
でヘンセルミキサーに入れ、3分間攪拌混合した後、口
径40m+nの単軸押出機で200℃にて溶融混練しペ
レタイズした。Example 6 and Comparative Example 6 With respect to 100 parts by weight of polypropylene of MFRIG, B
IT 0.1 part by weight, calcium stearate 0.1
Part by weight and propylene content 74 mol%, MFR14
The copolymers of propylene and butene ~1 in the proportions shown in Table 3 were put into a Hensel mixer, stirred and mixed for 3 minutes, and then melt-kneaded and pelletized at 200°C using a single-screw extruder with a diameter of 40 m+n.
ノズル径0.5+am 、ノズル数450個を有する紡
糸機により、前記原料を紡糸温度280℃、紡糸速度8
00m+/mjnの条件で4デニールの未延伸糸を紡糸
した6次にこの未延伸糸をステーブルファイバー製造設
備を用いて、延伸温度80℃、延伸倍率2倍の条件で延
伸し、捲縮を与えた後カットし2デニール長さSO+a
mのステーブルファイバーを得た。Using a spinning machine with a nozzle diameter of 0.5+am and 450 nozzles, the raw material was spun at a spinning temperature of 280°C and a spinning speed of 8.
6 Next, the undrawn yarn of 4 denier was spun under the conditions of 00m+/mjn. Next, the undrawn yarn was stretched using stable fiber manufacturing equipment at a stretching temperature of 80°C and a stretching ratio of 2 times, and crimping was performed. Cut after giving 2 denier length SO+a
m stable fibers were obtained.
このステーブルファイバーを巻き取り速度7.5■/■
inのカード機によりウェブとした後、加熱エンボスロ
ールによりウェブをポイントボンディングし不織布とし
た。Winding speed of this stable fiber is 7.5■/■
After forming a web using an in-line card machine, the web was point-bonded using a heated embossing roll to form a nonwoven fabric.
表3に不織布強力の結果を示す。Table 3 shows the results of the strength of the nonwoven fabric.
単一成分j#維であっても不織布加工温度幅が広くかつ
不織布強力の高い不織布が得られた。Even with a single component j# fiber, a nonwoven fabric with a wide nonwoven fabric processing temperature range and high nonwoven fabric strength was obtained.
比較例6
プロピレンとブテン−1の共重合体を使用しないこと以
外は実施例6と同様に実施した。Comparative Example 6 The same procedure as Example 6 was carried out except that the copolymer of propylene and butene-1 was not used.
表3に不織布強力の結果を示す。Table 3 shows the results of the strength of the nonwoven fabric.
実施例6と比べ不織布加工温度幅が狭くまた不織布強力
も低いことが判る。It can be seen that the nonwoven fabric processing temperature range is narrower and the nonwoven fabric strength is lower than in Example 6.
[発明の効果]
本発明によれば、従来の熱融着性繊維の欠点である不織
布加工温度条件幅の狭さが改善され、強力の高い不織布
が広い加工温度条件で製造できる。[Effects of the Invention] According to the present invention, the narrow range of processing temperature conditions for nonwoven fabrics, which is a drawback of conventional heat-fusible fibers, is improved, and a highly strong nonwoven fabric can be produced under a wide range of processing temperature conditions.
その結果、本発明の繊維は紙オムツを始め各種の用途に
通した不織布の原料として好適である。As a result, the fibers of the present invention are suitable as raw materials for nonwoven fabrics used in various applications including disposable diapers.
以 上that's all
Claims (2)
レン含有量が55〜85モル%のプロピレンとブテン−
1の共重合体を5〜100重量部添加した樹脂からなる
熱融着性繊維。(1) Propylene and butene with a propylene content of 55 to 85 mol% based on 100 parts by weight of polyolefin resin.
A heat-fusible fiber made of a resin to which 5 to 100 parts by weight of copolymer No. 1 is added.
ポリプロピレン樹脂若しくはポリブテン−1樹脂から選
ばれたいづれか一以上の樹脂からなる繊維を複合繊維の
一方の成分Aとし、ポリオレフィン樹脂100重量部に
対し、プロピレン含有量が55〜35モル%のプロピレ
ンとブテン−1の共重合体を5〜100重量部添加した
樹脂からなる繊維を複合織維の他方の成分Bとしてなり
、前記B成分の全部若しくは一部が該複合繊維の表面を
構成してなる熱融着性複合繊維。(2) High-density or linear low-density polyethylene resin,
One component A of the composite fiber is a fiber made of one or more resins selected from polypropylene resin or polybutene-1 resin, and propylene and butene with a propylene content of 55 to 35 mol% based on 100 parts by weight of polyolefin resin. - A fiber made of a resin to which 5 to 100 parts by weight of the copolymer of 1 is added is the other component B of the composite woven fiber, and all or part of the component B constitutes the surface of the composite fiber. Fusible composite fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11666190A JP2909837B2 (en) | 1990-05-02 | 1990-05-02 | Heat fusible fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11666190A JP2909837B2 (en) | 1990-05-02 | 1990-05-02 | Heat fusible fiber |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0418121A true JPH0418121A (en) | 1992-01-22 |
JP2909837B2 JP2909837B2 (en) | 1999-06-23 |
Family
ID=14692767
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11666190A Expired - Fee Related JP2909837B2 (en) | 1990-05-02 | 1990-05-02 | Heat fusible fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2909837B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998029586A1 (en) * | 1996-12-25 | 1998-07-09 | Chisso Corporation | Heat-fusible composite fiber and non-woven fabric produced from the same |
WO1999016947A1 (en) * | 1997-09-30 | 1999-04-08 | Kimberly-Clark Worldwide, Inc. | Crimped multicomponent filaments and spunbond webs made therefrom |
KR100291755B1 (en) * | 1998-04-21 | 2001-10-25 | 권순자 | Manufacturing method of low melting point heat-sealable filament yarn using low density polyethylene |
WO2011007875A1 (en) * | 2009-07-17 | 2011-01-20 | ダイワボウホールディングス株式会社 | Crimped composite fiber, and fibrous mass and textile product using the same |
-
1990
- 1990-05-02 JP JP11666190A patent/JP2909837B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998029586A1 (en) * | 1996-12-25 | 1998-07-09 | Chisso Corporation | Heat-fusible composite fiber and non-woven fabric produced from the same |
US6156679A (en) * | 1996-12-25 | 2000-12-05 | Chisso Corporation | Heat-fusible composite fiber and non-woven fabric produced from the same |
WO1999016947A1 (en) * | 1997-09-30 | 1999-04-08 | Kimberly-Clark Worldwide, Inc. | Crimped multicomponent filaments and spunbond webs made therefrom |
US6410138B2 (en) | 1997-09-30 | 2002-06-25 | Kimberly-Clark Worldwide, Inc. | Crimped multicomponent filaments and spunbond webs made therefrom |
KR100291755B1 (en) * | 1998-04-21 | 2001-10-25 | 권순자 | Manufacturing method of low melting point heat-sealable filament yarn using low density polyethylene |
WO2011007875A1 (en) * | 2009-07-17 | 2011-01-20 | ダイワボウホールディングス株式会社 | Crimped composite fiber, and fibrous mass and textile product using the same |
Also Published As
Publication number | Publication date |
---|---|
JP2909837B2 (en) | 1999-06-23 |
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