JPS63175113A - Blend structure of polyethylene with polypropylene - Google Patents
Blend structure of polyethylene with polypropyleneInfo
- Publication number
- JPS63175113A JPS63175113A JP558687A JP558687A JPS63175113A JP S63175113 A JPS63175113 A JP S63175113A JP 558687 A JP558687 A JP 558687A JP 558687 A JP558687 A JP 558687A JP S63175113 A JPS63175113 A JP S63175113A
- Authority
- JP
- Japan
- Prior art keywords
- linear low
- density polyethylene
- polypropylene
- spinning
- density
- 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
- -1 polyethylene Polymers 0.000 title claims abstract description 35
- 239000004743 Polypropylene Substances 0.000 title claims abstract description 28
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 26
- 239000000203 mixture Substances 0.000 title claims abstract description 21
- 239000004698 Polyethylene Substances 0.000 title description 10
- 229920000573 polyethylene Polymers 0.000 title description 9
- 229920000092 linear low density polyethylene Polymers 0.000 claims abstract description 30
- 239000004707 linear low-density polyethylene Substances 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 17
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000005977 Ethylene Substances 0.000 claims abstract description 6
- 230000004927 fusion Effects 0.000 claims abstract description 6
- 229920001577 copolymer Polymers 0.000 claims abstract description 4
- 239000000155 melt Substances 0.000 claims description 14
- 239000004745 nonwoven fabric Substances 0.000 abstract description 15
- 238000002156 mixing Methods 0.000 abstract description 4
- 238000002074 melt spinning Methods 0.000 abstract 2
- 238000009987 spinning Methods 0.000 description 25
- 239000000835 fiber Substances 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 9
- 229920001903 high density polyethylene Polymers 0.000 description 6
- 239000004700 high-density polyethylene Substances 0.000 description 6
- 229920001684 low density polyethylene Polymers 0.000 description 5
- 239000004702 low-density polyethylene Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 101000697856 Rattus norvegicus Bile acid-CoA:amino acid N-acyltransferase Proteins 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920006253 high performance fiber Polymers 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000013441 quality evaluation Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 239000011800 void material 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)
本発明は線状低密度ポリエチレンと結晶性ポリプロピレ
ンとのブレンド構造体に関するもので。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a blend structure of linear low density polyethylene and crystalline polypropylene.
特に柔らかさと風合においてより好適な不織布を提供す
るものである。In particular, it provides a nonwoven fabric that is more suitable in terms of softness and texture.
(従来の技術)
従来より異なる溶融温度を有する繊維を含有する不織布
は当業界ではよく知られている。低い溶融温度を有する
繊維は高い溶融温度を有する繊維同士を結合させる接着
剤として作用する。ポリエチレンとポリプロピレンの含
有繊維は比較的低い溶融温度とかその他の望ましい特性
を有しているので不織布としてよく使用される。しかし
ながらポリエチレンは高速で製糸しにくいため製糸とウ
ェブ作成を連続的にするいわゆるスパンボンド方式でポ
リエチレンとポリプロピレンを含有する不織布を得にく
かった。製糸性に劣るため接着剤としては不満足であっ
た。BACKGROUND OF THE INVENTION Nonwoven fabrics containing fibers having conventionally different melting temperatures are well known in the art. Fibers with lower melting temperatures act as adhesives to bond fibers with higher melting temperatures. Polyethylene and polypropylene containing fibers are often used as nonwoven fabrics because they have relatively low melting temperatures and other desirable properties. However, since polyethylene is difficult to spin at high speeds, it has been difficult to obtain nonwoven fabrics containing polyethylene and polypropylene using the so-called spunbond method, which involves continuous spinning and web preparation. It was unsatisfactory as an adhesive because of its poor spinning properties.
またポリエチレン繊維は低密度ポリエチレンや高密度ポ
リエチレンが用いられてきたが最近に至り特開昭60−
209010号公報及び特開昭60−1941)3号公
報に示されるようにエチレンとオクテン−1を共重合し
て得られる線状低密度ポリエチレンが用いられるように
なってきた。In addition, low-density polyethylene and high-density polyethylene have been used as polyethylene fibers, but recently,
As shown in JP-A No. 209010 and JP-A-60-1941), linear low-density polyethylene obtained by copolymerizing ethylene and octene-1 has come to be used.
(発明が解決しようとする問題点) 近年スパンボンド方式で不織布を得るために。(Problem to be solved by the invention) In recent years, spunbond method has been used to obtain nonwoven fabrics.
あるいはマルチフィラメントの糸条などを得る工程を簡
略化して製造原価を低減するために、紡糸の高速化の(
順向が強くなってきている。しかし密度及びメルトイン
デックスを規定した上記両公報に記載の方法の線状低密
度ポリエチレン単体では高速紡糸に要求される可紡性は
高温領域では満足できるものの、その可紡性は時間的安
定性に対しなお不満足であった。すなわち紡糸温度が線
状低密度ポリエチレンの溶融温度よりかなり高くするこ
とにより高速吸引は可能で細いデニールの繊維は確かに
得ることは可能であるが、経時的に口金面が汚れ、糸面
がりや断糸というトラブルが生じる。Alternatively, in order to simplify the process of obtaining multifilament threads and reduce manufacturing costs,
The trend is becoming stronger. However, although the spinnability required for high-speed spinning can be satisfied in the high-temperature region using the linear low-density polyethylene alone obtained by the methods described in both of the above publications that specify the density and melt index, the spinnability is limited by the temporal stability. However, they were still dissatisfied. In other words, by setting the spinning temperature considerably higher than the melting temperature of linear low-density polyethylene, high-speed suction is possible and it is certainly possible to obtain fine denier fibers, but over time the spinneret surface gets dirty, the thread surface becomes curly, and it is possible to obtain fine denier fibers. The problem of thread breakage occurs.
本発明の目的は上記問題点を解消し、製糸において高速
吸引ができて操業性が経時的にも安定して製糸性できる
ブレンド構造体を提供することにある。An object of the present invention is to solve the above-mentioned problems and provide a blend structure that can perform high-speed suction during yarn spinning and has stable operability over time.
(問題点を解決するだめの手段および作用)すなわち本
発明は、エチレンとオクテン−1との線状低密度コポリ
マーでオクテン−1を実質的に1〜15重量%含有し、
密度が0.900〜0.940g/cm3,メルトイン
デツクスがASTMのD−1238(E)の方法で測定
して25〜100g/10分であり、融解熱が25ca
l/g以上からなる線状低密度ポリエチレンが99〜5
0重量%とメルトインデックスがASTMのD−123
8(E)の方法で測定して20g/10分より小さい結
晶性ボyプロピレンが1〜50重景%とから構成され、
溶融紡糸されているブレンド構造体を要旨とするもので
ある。(Means and effects for solving the problem) That is, the present invention is a linear low-density copolymer of ethylene and octene-1 containing substantially 1 to 15% by weight of octene-1,
The density is 0.900 to 0.940 g/cm3, the melt index is 25 to 100 g/10 minutes as measured by ASTM D-1238 (E) method, and the heat of fusion is 25 ca.
Linear low density polyethylene consisting of l/g or more is 99-5
0% by weight and melt index ASTM D-123
8(E), consisting of 1 to 50 weight percent of crystalline void propylene smaller than 20 g/10 min, as measured by the method of 8(E);
The gist is a melt-spun blend structure.
本発明においてメルトインデックスはA S T Mの
D −1238(E)の方法で測定する。In the present invention, the melt index is measured by ASTM method D-1238(E).
本発明において融解熱は以下のようにして測定したもの
である。パーキンエルマ(Perkin−Elmer)
製DSC−2C型分析器を使用し、試料約5mgを採取
し、走査速度(Scan Rate)を20℃/分とし
室温より昇温しで得られるDSC曲線から同装置マニア
ルに従って求める。In the present invention, the heat of fusion is measured as follows. Perkin-Elmer
Approximately 5 mg of a sample is collected using a DSC-2C type analyzer manufactured by Kogyo Co., Ltd., and the sample is determined from a DSC curve obtained by raising the temperature from room temperature at a scan rate of 20° C./min according to the device manual.
本発明におけるブレンド構造体に用いられる線状低密度
ポリエチレン単体は、エチレンとオクテン−1の他に、
オクテン−1の重量の15重量%以下の他のα−オレフ
ィンを含有していてもよい。また該線状低密度ポリエチ
レンに吸湿剤や潤滑剤、顔料、染料、安定剤、難燃剤等
の添加剤を加えてもよい。In addition to ethylene and octene-1, the linear low-density polyethylene used in the blend structure of the present invention includes:
It may contain up to 15% by weight of other α-olefins based on the weight of octene-1. Further, additives such as a moisture absorbent, a lubricant, a pigment, a dye, a stabilizer, and a flame retardant may be added to the linear low-density polyethylene.
本発明において線状低密度ポリエチレンのオクテン−1
の含有量が15重量%を超えると細い繊度の繊維が得に
(くなり、逆にこれが1重量%未満の場合は得られる繊
維は硬くなり9例えば不織布のような製品になってから
の風合がよくない。In the present invention, octene-1 of linear low density polyethylene
If the content exceeds 15% by weight, finer fineness fibers will be obtained.On the other hand, if it is less than 1% by weight, the resulting fibers will be stiff. The fit is not good.
本発明において線状低密度ポリエチレンの密度が0.9
40g/cm3を超えると繊維の軽量化が図れず逆に0
.9008/cm’未満では高性能の繊維を得ることは
困難である。In the present invention, the density of linear low density polyethylene is 0.9
If it exceeds 40g/cm3, it will not be possible to reduce the weight of the fiber, and on the contrary, the weight will be 0.
.. If it is less than 9008/cm', it is difficult to obtain high performance fibers.
本発明において線状低密度ポリエチレンのメルトインデ
ックスを25〜100g/10分に限定した理由は、線
状低密度ポリエチレン単体で製糸すればメルトインデッ
クス25g/10分未満では吐出糸条の変形がスムース
にいかず、その結果として製糸工程における高速吸引は
不可能である。また100g/10分以上では粘性があ
まりにも小さいため繊径斑が発生し、得られた繊維の性
能が劣る。The reason why the melt index of linear low-density polyethylene is limited to 25 to 100 g/10 minutes in the present invention is that if linear low-density polyethylene is used alone, the deformation of the discharged yarn will be smooth if the melt index is less than 25 g/10 minutes. As a result, high-speed suction in the spinning process is not possible. Moreover, if it exceeds 100 g/10 minutes, the viscosity is too low, causing fiber diameter unevenness, and the performance of the obtained fibers is poor.
本発明におけるブレンド構造体はポリエチレンとポリプ
ロピレンの両者の溶融粘性が特に重要な要件となる。す
なわち線状低密度ポリエチレンのメルトインデックスが
25g/10分未満では吐出糸条の溶融弾性があがり線
状低密度ポリエチレン単体の製糸性よりも劣る。そして
線状低密度ポリエチレンのメルトインデックスが100
g/10分以上であると粘性があまりにも異なるため均
一なブレンド状態が得られない。その結果として吐出糸
条が口金直下で断糸するという重大な欠陥を生じる。The melt viscosity of both polyethylene and polypropylene is a particularly important requirement for the blend structure in the present invention. In other words, if the melt index of the linear low density polyethylene is less than 25 g/10 minutes, the melt elasticity of the discharged yarn will increase and the spinability will be inferior to that of the linear low density polyethylene alone. And the melt index of linear low density polyethylene is 100.
g/10 minutes or more, the viscosity is too different and a uniform blend cannot be obtained. As a result, a serious defect occurs in that the discharged yarn breaks just below the nozzle.
上記の理由で線状低密度ポリエチレンのメルトインデッ
クスは好ましくは35〜80g/10分、更により好ま
しくは40〜70g/10分の範囲がよい。線状低密度
ポリエチレンの融解熱が25ca l/ g未満である
と製糸性は劣る。For the above reasons, the melt index of the linear low density polyethylene is preferably in the range of 35 to 80 g/10 minutes, even more preferably in the range of 40 to 70 g/10 minutes. If the heat of fusion of the linear low-density polyethylene is less than 25 cal/g, the spinning properties will be poor.
本発明のブレンド構造体に用いるのに適当な結晶性ポリ
プロピレンはイソタクチックポリプロピレンであり、そ
のメルトインデックスは20g/10分以下のものに限
定される。なぜならばこの範囲を外れると線状低密度ポ
リエチレンとのブレンドが均一になされない。すなわち
両成分のブレンド機構におけるポリプロピレンセグメン
トが線状低密度ポリエチレン中で繊維軸方向において「
流れすぎ」のために製糸工程における吸引速度は低下す
る。The crystalline polypropylene suitable for use in the blend structure of the present invention is isotactic polypropylene, which is limited to a melt index of 20 g/10 minutes or less. This is because, if it is outside this range, it will not be blended uniformly with linear low density polyethylene. In other words, the polypropylene segment in the blending mechanism of both components is "
Due to "too much flow", the suction speed in the yarn spinning process decreases.
本発明による構造体を得るには線状低密度ポリエチレン
と結晶性ポリプロピレンとを一諸にブレンドし1次いで
従来公知の紡糸設備で紡糸すればよい。しかし線状低密
度ポリエチレンと結晶性ポリプロピレンのブレンド比率
も高速吸引性に太き(関与する。綿状低密度ポリエチレ
ン単体やポリプロピレン単体の製糸工程における吸引速
度は本発明のブレンド構造体の場合はども高速にならな
い。また結晶性ポリプロピレンの量が線状低密度ポリエ
チレンの量より多(なると逆に製糸性は劣る結果となる
。In order to obtain the structure according to the present invention, linear low density polyethylene and crystalline polypropylene may be blended together and then spun using conventional spinning equipment. However, the blend ratio of linear low-density polyethylene and crystalline polypropylene also has a large effect on high-speed suction properties. The speed cannot be increased. Also, if the amount of crystalline polypropylene is greater than the amount of linear low-density polyethylene (on the contrary, the spinning properties will be poor).
更にまた線状低密度ポリエチレンの代わりに高密度ポリ
エチレン又は低密度ポリエチレンに置き換え結晶性ポリ
プロピレンとのブレンド構造体についてその製糸性につ
いて比較してみるとその吸引速度は製糸不能であったり
、製糸できても高速では行えない。Furthermore, when comparing the yarn-spinning properties of linear low-density polyethylene replaced with high-density polyethylene or low-density polyethylene and blended structures with crystalline polypropylene, the suction speed was found to be either impossible or impossible to spin. can't be done at high speed either.
本発明のブレンド機構は繊維断面及び軸方向に対し線状
低密度ポリエチレンの海成分にポリプロピレンが島成分
として位置する。製糸性に大きく起因するのは島成分の
大きさである。両成分の溶融粘性が近すぎるとかなり小
さな島成分となる。In the blending mechanism of the present invention, polypropylene is located as an island component in a sea component of linear low-density polyethylene with respect to the fiber cross section and axial direction. The size of the island component is largely responsible for the silk-spinning property. If the melt viscosities of both components are too close, a fairly small island component will result.
その結果として溶融弾性が上がりすぎ高速吸引には耐え
られない。逆にあまりにも異なりずき゛ると島成分が大
きくなりすぎ2両成分がマクロな形状で吐出されるため
同様に製糸工程で高速吸引に耐えられない。As a result, the melt elasticity becomes too high to withstand high-speed suction. On the other hand, if the difference is too large, the island component becomes too large and both components are discharged in a macroscopic shape, which similarly cannot withstand high-speed suction in the silk-spinning process.
本発明のブレンド構造体を製造するにおいて紡糸温度は
次のような考慮を払えばよい。線状低密度ポリエチレン
に結晶性ポリプロピレンをブレンドすることにより低い
紡糸温度でも高速吸引が可能であり、また従来より問題
となっている口金の汚れを防止することが可能である。In producing the blend structure of the present invention, the following considerations may be taken into consideration regarding the spinning temperature. By blending crystalline polypropylene with linear low-density polyethylene, high-speed suction is possible even at low spinning temperatures, and it is also possible to prevent staining of the spinneret, which has been a problem in the past.
線状低密度ポリエチレン単体は高速吸引性を考慮すれば
250℃付近が、結晶性ポリプロピレン単体は270℃
付近が通常適用されるが5本発明ブレンド構造体の紡糸
温度としては200〜250℃更に好ましくは210〜
230℃が適用される。なお繊維断面形状は丸に限らず
スリット部を有する異型あるいは中空断面でも何ら規制
するものでない。Linear low-density polyethylene alone has a temperature of around 250°C, considering high-speed suction properties, while crystalline polypropylene alone has a temperature of 270°C.
The spinning temperature of the blend structure of the present invention is usually 200 to 250°C, and more preferably 210 to 250°C.
230°C is applied. Note that the cross-sectional shape of the fibers is not limited to a round shape, and may be an irregular shape having a slit or a hollow cross-section.
本発明によるブレンド構造物からの不織布は線状低密度
ポリエチレン単体のものやポリプロピレン単体のものよ
り引張強力に優れ、ソフト性も十分であり、更にポリプ
ロピレン特有の「ぬめり」が全くない良好な風合を有し
ている。The nonwoven fabric made from the blend structure of the present invention has superior tensile strength and softness compared to linear low-density polyethylene alone or polypropylene alone, and has a good texture without any "sliminess" characteristic of polypropylene. have.
本発明によるブレンド構造物からの不織布を得るには製
糸工程とウェブ作成工程に分けて得ても差支えないが1
次のように連続工程によって得る方が生産性の点で好ま
しい。In order to obtain a nonwoven fabric from the blend structure according to the present invention, it is possible to obtain the nonwoven fabric by dividing the yarn spinning process and the web making process.
From the viewpoint of productivity, it is preferable to obtain it by a continuous process as described below.
その方法はいわゆるスパンボンド方式で本発明ブレンド
構造体を高速吸引ガンで吸引開繊し移動する金網状物の
上に堆積させウェブを形成し1次いでエンボスロールに
導き圧縮、加熱処理を施し不織布を得るものである。The method is the so-called spunbond method, in which the blend structure of the present invention is opened by suction with a high-speed suction gun, deposited on a moving wire mesh to form a web, and then passed to an embossing roll where it is compressed and heated to form a nonwoven fabric. It's something you get.
(実施例) 次ぎに実施例により具体的に説明する。(Example) Next, the present invention will be specifically explained using examples.
実施例1
第1表のとおり種々のポリエチレンとポリプロピレンを
準備した。Example 1 Various types of polyethylene and polypropylene were prepared as shown in Table 1.
第1表(続)
(注)第1表において線状低密度ポリエチレンをLLD
PE、低密度ポリエチレンをLDPE、高密度ポリエチ
レンをHDPEで示す。またポリプロピレンをPPで示
す。Table 1 (continued) (Note) In Table 1, linear low density polyethylene is
PE, low density polyethylene is shown as LDPE, and high density polyethylene is shown as HDPE. Further, polypropylene is indicated by PP.
次に第2表に示す条件で製糸した。第2表において高密
度ポリエチレンとポリプロピレンのブレンド比の欄のA
〜Gのアルファベットの記号は第1表の試料記号と対応
している。Next, yarn spinning was carried out under the conditions shown in Table 2. A in the blend ratio column of high density polyethylene and polypropylene in Table 2
The alphabetical symbols of ~G correspond to the sample symbols in Table 1.
第2表
各試料とも0.4φの孔径で孔数が80の紡糸口金を用
い、1孔当たり吐出量は1.5g/分とした。Table 2 For each sample, a spinneret with a hole diameter of 0.4φ and 80 holes was used, and the discharge rate per hole was 1.5 g/min.
製糸性の評価結果を第3表に示し、糸質の評価結果を第
4表に示す。Table 3 shows the evaluation results for yarn spinning properties, and Table 4 shows the evaluation results for yarn quality.
第3表 製糸性の評価結果
(注)■第3表において不能とあるのは製糸不能のこと
である。Table 3 Results of evaluation of silk-spinning properties (Note) ■ In Table 3, "impossible" means that silk-spinning is impossible.
■口金汚れは糸条を吐出し1時間後に口金面を観察する
方法によった。■ The staining of the cap was determined by observing the surface of the cap 1 hour after discharging the thread.
■糸切れの評価は1時間当たりの糸切れ回数で評価した
。■Evaluation of yarn breakage was based on the number of yarn breakages per hour.
第4表 糸質の評価結果
第1〜4表から明らかなように、ポリエチレンとポリプ
ロピレンのブレンド構造体で高性能のものを操業性よ(
得るには本発明の範囲外では決して得ることはできない
ことが分かる。Table 4 Results of yarn quality evaluation As is clear from Tables 1 to 4, high-performance blend structures of polyethylene and polypropylene have improved operability (
It can be seen that it cannot be obtained in any way outside the scope of the present invention.
例えば比較例寛1の線状低密度ポリエチレン単体と本発
明による試料患3のブレンド構造体を比較すると両者と
も吸引速度、糸性能、風合とも優れている。しかしなが
ら本発明例の隘3は製糸性は良好であるが比較例のNU
LLは口金汚れが多く。For example, when the linear low-density polyethylene alone of Comparative Example Kan 1 is compared with the blended structure of Sample No. 3 according to the present invention, both are excellent in suction speed, yarn performance, and texture. However, NU of the example of the present invention has good reeling properties, but NU of the comparative example
LL has a lot of dirt on the base.
これに起因する糸切れが見られた。ブレンド比率におい
ても比較例覧5と比較例1)h6のようにポリプロピレ
ンが重量%で50%を超えると逆に製糸性は低下し、ま
た風合においても「ぬめり」が発生する。比較例1)h
8と比較例患9.比較例N1)2は本発明の範囲以外の
メルトインデックスを示すポリエチレンやポリプロピレ
ンを用いた場合であり。Thread breakage caused by this was observed. As for the blend ratio, if the polypropylene content exceeds 50% by weight as in Comparative Example List 5 and Comparative Example 1)h6, the spinning property deteriorates and the texture also becomes "slimy". Comparative example 1) h
8 and comparative example patient 9. Comparative Examples N1) and 2 are cases in which polyethylene or polypropylene having a melt index outside the range of the present invention is used.
比較例1)&lIOと比較例mllは低密度ポリエチレ
ンや高密度ポリエチレンを用いた場合であり、いずれも
それらの製糸性の悪いことが分かる。Comparative Example 1) &lIO and Comparative Example mll are cases where low-density polyethylene and high-density polyethylene were used, and it can be seen that both have poor spinning properties.
実施例2
線状低密度ポリエチレン75重量%と結晶性ポリプロピ
レン25重量%のブレンドで、紡糸温度220℃、吸引
速度8800m/分として、その他実施例1の1)13
と同じの条件で吸引開繊し移動する金網状物の上に堆積
させ、ウェブを形成し、ついでエンボスロールに導き圧
縮、加熱処理を与えて不織布とした。得られた不織布の
性能は優れており、風合の非常に良好なものが得られた
。その不織布の性能を第5表に示す。Example 2 A blend of 75% by weight of linear low-density polyethylene and 25% by weight of crystalline polypropylene, with a spinning temperature of 220°C and a suction speed of 8800 m/min, as well as 1) 13 of Example 1.
The fibers were opened under suction under the same conditions as above and deposited on a moving wire mesh to form a web, which was then introduced to an embossing roll and subjected to compression and heat treatment to form a nonwoven fabric. The performance of the obtained nonwoven fabric was excellent, and the fabric had a very good feel. The performance of the nonwoven fabric is shown in Table 5.
第5表における物性値の測定法は次のとおりである。The method of measuring the physical property values in Table 5 is as follows.
引張強力はJIS L−1096のストリップ法に串じ
。The tensile strength is determined by the strip method of JIS L-1096.
巾30mm、長さ100mmの試験片の最大引張強力を
測定した。The maximum tensile strength of a test piece with a width of 30 mm and a length of 100 mm was measured.
トータルハンドは柔らかさを示すもので、JIS L−
1096のハンド・オ・メータ法に準じ、スロット巾1
0mmで測定した。Total hand indicates softness and is JIS L-
According to the hand-o-meter method of 1096, slot width 1
Measured at 0 mm.
(発明の効果)
本発明で得られるブレンド構造体は操業性よく生産され
、製糸後に不織布とすると、該構造体は柔らかさと風合
に優れているから、使い捨ておむつの内張りのような用
途に特に適した不織布が得られる。(Effects of the Invention) The blended structure obtained by the present invention can be produced with good operability, and when made into a nonwoven fabric after spinning, the structure has excellent softness and texture, so it is particularly suitable for applications such as the lining of disposable diapers. A suitable nonwoven fabric is obtained.
Claims (1)
ーでオクテン−1を実質的に1〜15重量%含有し,密
度が0.900〜0.940g/cm^3,メルトイン
デツクスがASTMのD−1238(E)の方法で測定
して25〜100g/10分であり,融解熱が25ca
l/g以上からなる線状低密度ポリエチレンが99〜5
0重量%とメルトインデツクスがASTMのD−123
8(E)の方法で測定して20g/10分より小さい結
晶性ポリプロピレンが1〜50重量%とから構成され,
溶融紡糸されていることを特徴とするブレンド構造体。(1) A linear low-density copolymer of ethylene and octene-1, containing substantially 1 to 15% by weight of octene-1, with a density of 0.900 to 0.940 g/cm^3, and a melt index of ASTM. It is measured by the method of D-1238 (E) of 25 to 100 g/10 minutes, and the heat of fusion is 25 ca.
Linear low density polyethylene consisting of l/g or more is 99-5
0% by weight and melt index is ASTM D-123
8(E), consisting of 1 to 50% by weight of crystalline polypropylene smaller than 20 g/10 minutes, as measured by the method of 8(E),
A blend structure characterized by being melt-spun.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62005586A JPH0653977B2 (en) | 1987-01-12 | 1987-01-12 | Method for producing fiber having a blend structure of polyethylene and polypropylene |
DE3888859T DE3888859T2 (en) | 1987-01-12 | 1988-01-12 | Bicomponent fiber made of polyolefin and non-woven fabric made from this fiber. |
US07/142,962 US4874666A (en) | 1987-01-12 | 1988-01-12 | Polyolefinic biconstituent fiber and nonwove fabric produced therefrom |
EP88300201A EP0277707B1 (en) | 1987-01-12 | 1988-01-12 | Polyolefinic biconstituent fiber and nonwoven fabric produced therefrom |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62005586A JPH0653977B2 (en) | 1987-01-12 | 1987-01-12 | Method for producing fiber having a blend structure of polyethylene and polypropylene |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6000641A Division JP2533289B2 (en) | 1994-01-10 | 1994-01-10 | Fiber made of a blended structure of polyethylene and polypropylene |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63175113A true JPS63175113A (en) | 1988-07-19 |
JPH0653977B2 JPH0653977B2 (en) | 1994-07-20 |
Family
ID=11615346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62005586A Expired - Fee Related JPH0653977B2 (en) | 1987-01-12 | 1987-01-12 | Method for producing fiber having a blend structure of polyethylene and polypropylene |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0653977B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06166111A (en) * | 1992-11-30 | 1994-06-14 | Kao Corp | Surface material of absorbent article and manufacture of the same |
JP2012106177A (en) * | 2010-11-17 | 2012-06-07 | Mitsubishi Paper Mills Ltd | Semipermeable membrane support |
JP2016532021A (en) * | 2013-09-19 | 2016-10-13 | ダウ グローバル テクノロジーズ エルエルシー | Small diameter polyolefin fiber |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5936147A (en) * | 1982-08-23 | 1984-02-28 | Mitsui Petrochem Ind Ltd | Polyethylene composition |
JPS5982406A (en) * | 1982-10-28 | 1984-05-12 | Nippon Petrochem Co Ltd | Polyolefin yarn |
JPS60194113A (en) * | 1984-02-17 | 1985-10-02 | ザ ダウ ケミカル カンパニー | Wettable olefine polymer fiber |
-
1987
- 1987-01-12 JP JP62005586A patent/JPH0653977B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5936147A (en) * | 1982-08-23 | 1984-02-28 | Mitsui Petrochem Ind Ltd | Polyethylene composition |
JPS5982406A (en) * | 1982-10-28 | 1984-05-12 | Nippon Petrochem Co Ltd | Polyolefin yarn |
JPS60194113A (en) * | 1984-02-17 | 1985-10-02 | ザ ダウ ケミカル カンパニー | Wettable olefine polymer fiber |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06166111A (en) * | 1992-11-30 | 1994-06-14 | Kao Corp | Surface material of absorbent article and manufacture of the same |
JP2012106177A (en) * | 2010-11-17 | 2012-06-07 | Mitsubishi Paper Mills Ltd | Semipermeable membrane support |
JP2016532021A (en) * | 2013-09-19 | 2016-10-13 | ダウ グローバル テクノロジーズ エルエルシー | Small diameter polyolefin fiber |
Also Published As
Publication number | Publication date |
---|---|
JPH0653977B2 (en) | 1994-07-20 |
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