JPH0359169A - Hot-weldable fiber - Google Patents
Hot-weldable fiberInfo
- Publication number
- JPH0359169A JPH0359169A JP1192490A JP19249089A JPH0359169A JP H0359169 A JPH0359169 A JP H0359169A JP 1192490 A JP1192490 A JP 1192490A JP 19249089 A JP19249089 A JP 19249089A JP H0359169 A JPH0359169 A JP H0359169A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- hot
- polyoxyalkylene
- polyoxyethylene
- weight
- 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.)
- Pending
Links
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明はソフトな風合でかつ水洗耐久性に優れた親水性
を呈する熱接着性繊維に関する。更に詳しくは、製綿工
程、カード工程等でのスカム発生。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a thermoadhesive fiber that has a soft feel and exhibits hydrophilic properties with excellent water wash durability. More specifically, scum occurs in the cotton manufacturing process, carding process, etc.
静電気発生が少なく工程安定性が良好で、かつウェブ斑
等のない良品質の不織布が得られる熱接着性繊維に関す
る。The present invention relates to a heat-adhesive fiber that generates little static electricity, has good process stability, and provides a high-quality nonwoven fabric without web unevenness.
〈従来技術〉
従来より、不織布用として各種の熱接着性繊維が提案さ
れており、主として鞘/芯型の複合繊維、例えば、低融
点ポリエステル/ポリエチレンテレフタレート、ポリエ
チレン/ポリプロピレン、ポリエチレン/ポリエチレン
テレフタレート等が使用されている。近年、これらの使
用される分野も拡大しつつあり、中でも食品・家庭用の
ティーバッグ、化粧用パフ、ウェットティッシュ、衛生
医療用として、生理ナプキン、紙オムツ等の表面材。<Prior art> Various heat-adhesive fibers have been proposed for use in nonwoven fabrics, mainly sheath/core type composite fibers, such as low-melting point polyester/polyethylene terephthalate, polyethylene/polypropylene, polyethylene/polyethylene terephthalate, etc. It is used. In recent years, the fields in which they are used have been expanding, particularly as surface materials for tea bags for food and household use, cosmetic puffs, wet tissues, sanitary napkins, disposable diapers, etc. for hygiene and medical use.
オムツライナー、湿布基布等に使用される熱接着性繊維
には、水洗耐久性に優れた親水性、さらにはソフトな風
合が要求されている。Heat-adhesive fibers used for diaper liners, poultice base fabrics, etc. are required to have hydrophilic properties with excellent washability and a soft texture.
一般にソフト仕上げの可能な熱接着性繊維は、ポリマー
改質された熱接着成分ポリマーが使用されるため、容易
に変形してガイド、ローラー、針布等糸導部に対して、
通常の合成繊維よりはるかに接触面積が大きくなる。そ
の結果、繊維・金属間の摩擦が著しく大きくなってスカ
ムが極めて発生し易くなり、製綿工程の安定性低下、ひ
いては最終的に得られる不織布の品質低下の要因となっ
ている。さらには、紡績等の後工程においては、静電気
が発生し易く、かつカード、シリンダーローラー等への
捲付が多発する傾向がある。In general, heat-adhesive fibers that can be soft-finished use polymer-modified heat-adhesive component polymers, so they are easily deformed and cannot be attached to thread guides such as guides, rollers, and clothing.
The contact area is much larger than that of ordinary synthetic fibers. As a result, the friction between the fibers and the metal increases significantly, making it extremely easy to generate scum, which causes a decrease in the stability of the cotton-making process and, ultimately, a decrease in the quality of the nonwoven fabric finally obtained. Furthermore, in post-processes such as spinning, static electricity tends to be generated and winding around cards, cylinder rollers, etc. tends to occur frequently.
一方、熱接着性繊維に親水性を付与するには、親水性化
合物を繊維表面に付着させる方法が簡便であり、一般に
採用されている。かかる方法としては、例えば、特開昭
54−153872号公報には、硫酸エステル塩類、リ
ン酸エステル塩類、及びスルホン酸塩類から選ばれる1
種の化合物を含むアニオン系界面活性剤で5.ポリプロ
ピレン多孔質膜を処理する方法が開示されている。しか
し、この場合、親水性の耐久性に劣るという問題がある
。又、特開昭64−6173号公報には、ソルビタント
リ脂肪酸エステル化合物等を用いて処理する方法が開示
されているが、処理剤が接着界面に偏在し易いため接着
を阻害するといった問題がある。又、特開昭63−30
3184号公報には、ポリオキシアルキレン変性シリコ
ンを30重量%以上含む処理剤で、ポリオレフィン系熱
接着性繊維を処理することが開示されている。成程この
方法によれば、水洗耐久性に優れた親水性を呈するとと
もに、カード工程通過性の改善された熱接着性繊維が得
られる。しかしながら、本発明者らの検討によれば、製
綿工程、不織布製造工程でのスカム発生が大きく、工程
安定性の面では未だ不十分なものであった。さらには、
該繊維に機械捲縮が安定に付与できない、あるいは、日
付斑のない品質の安定した不織布が得難いといった問題
点もあった。On the other hand, in order to impart hydrophilicity to heat-adhesive fibers, a method of attaching a hydrophilic compound to the fiber surface is simple and generally employed. As such a method, for example, JP-A-54-153872 discloses that one selected from sulfuric acid ester salts, phosphoric acid ester salts, and sulfonic acid salts.
5. With an anionic surfactant containing a species compound. A method of treating a porous polypropylene membrane is disclosed. However, in this case, there is a problem that the durability of hydrophilicity is poor. Furthermore, JP-A No. 64-6173 discloses a treatment method using a sorbitan trifatty acid ester compound, etc., but there is a problem that the treatment agent tends to be unevenly distributed at the adhesive interface, inhibiting adhesion. . Also, JP-A-63-30
Publication No. 3184 discloses treating polyolefin thermal adhesive fibers with a treatment agent containing 30% by weight or more of polyoxyalkylene-modified silicone. According to this method, a heat-adhesive fiber can be obtained which exhibits hydrophilicity with excellent water washing durability and has improved passability through a carding process. However, according to studies conducted by the present inventors, scum generation was large in the cotton manufacturing process and the nonwoven fabric manufacturing process, and the process stability was still insufficient. Furthermore,
There are also problems in that mechanical crimp cannot be stably applied to the fibers, or that it is difficult to obtain nonwoven fabrics of stable quality without date spots.
〈発明の目的〉
本発明は、かかる背景に鑑みなされたもので、その目的
は、ソフトな風合と水洗耐久性に優れた親水性を呈しな
がら、製綿工程、不織布製造工程等での工程安定性に優
れ、かつ品質の良好(目付斑、接着強度)な不織布の得
られる熱接着性繊維を提供することにある。<Purpose of the Invention> The present invention was made in view of the above background, and its purpose is to provide a soft texture and hydrophilicity with excellent water washing durability, while providing a material that can be used in cotton manufacturing processes, nonwoven fabric manufacturing processes, etc. It is an object of the present invention to provide a thermally bondable fiber from which a nonwoven fabric with excellent stability and good quality (unevenness and adhesive strength) can be obtained.
〈発明の構成〉
本発明者らは、前記目的を達成すべく鋭意検討した結果
、驚くべきことに、ポリオキシアルキレン変性シリコン
を従来公知のものより極めて少なくするとともに、極め
て特定した範囲内のくポリオキシアルキレン〉アルキル
燐酸エステルアルカリ金属塩を併用した処理剤を付与す
ることにより、前記目的を同時に達成できることを知り
、本発明に到達した。<Structure of the Invention> As a result of intensive studies to achieve the above object, the present inventors have surprisingly found that the amount of polyoxyalkylene-modified silicone can be significantly reduced compared to conventionally known silicones, and that polyoxyalkylene-modified silicone can be used within a very specific range. It was discovered that the above objectives can be achieved at the same time by applying a treatment agent containing an alkali metal salt of polyoxyalkylene>alkyl phosphate ester, and the present invention was achieved.
すなわち、本発明によれば、融点が50〜200℃の熱
可塑性重合体を熱接着成分とし、かつその少なくとも5
0重量%がポリオレフィン系重合体である熱接着性繊維
において、該繊維表面に下記(A)及び(B)成分を含
有する処理剤が、処理剤有効成分として0.05〜5重
量%付着していることを特徴とする熱接着性繊維。That is, according to the present invention, a thermoplastic polymer having a melting point of 50 to 200° C. is used as a thermal adhesive component, and at least 5
In a heat-adhesive fiber in which 0% by weight is a polyolefin polymer, a treatment agent containing the following components (A) and (B) adheres to the surface of the fiber in an amount of 0.05 to 5% by weight as an active ingredient of the treatment agent. A thermoadhesive fiber characterized by:
(A)シリコン含有率が50%以下、ポリオキシアルキ
レン中のポリオキシエチレン含有率が40%以上で、分
子量がi、ooo〜100.000のポリオキシアルキ
レン変性シリコン=5〜20重量%(B)平均炭素数が
8〜10のアルキル基であってオキシエチレン付加モル
数が0〜15の〈ポリオキシエチレン〉アルキル基で、
燐酸化度が0.5〜1.0、酸価がθ〜150の、(ポ
リオキシエチレン〉アルキル燐酸エステルのアルカリ金
属塩=25〜95重量%
が提供される。(A) Polyoxyalkylene-modified silicone with silicon content of 50% or less, polyoxyethylene content in polyoxyalkylene of 40% or more, and molecular weight of i, ooo to 100.000 = 5 to 20% by weight (B ) A <polyoxyethylene> alkyl group having an average carbon number of 8 to 10 and an oxyethylene addition mole number of 0 to 15,
An alkali metal salt of (polyoxyethylene>alkyl phosphate ester=25 to 95% by weight) having a degree of phosphorylation of 0.5 to 1.0 and an acid value of θ to 150 is provided.
本発明で用いられるポリオキシアルキレン変性シリコン
(A成分〉としては、下記一般式で表わされるものがあ
げられる。Examples of the polyoxyalkylene-modified silicone (component A) used in the present invention include those represented by the following general formula.
MeX−RMe
(式中、Meはメチル基、Xはメチレン、プロピレン、
N−(アミノエチル〉メチルイミノ、又はN−(アミノ
プロピル〉プロピルイミノ、Rはポリオキシアルキレン
基、n及びmはシリコン含有率が50%以下で分子量が
1.000〜100.000となる範囲で選ばれる数を
示す。)
かかる変性シリコーン中のシリコン含有率は50%以下
である必要があり、50%を越えると十分な親水性は得
られず好ましくない。MeX-RMe (wherein, Me is a methyl group, X is methylene, propylene,
N-(aminoethyl>methylimino, or N-(aminopropyl>propylimino), R is a polyoxyalkylene group, n and m are in the range where the silicon content is 50% or less and the molecular weight is 1.000 to 100.000. (The selected number is shown.) The silicon content in such modified silicone must be 50% or less; if it exceeds 50%, sufficient hydrophilicity cannot be obtained and is not preferred.
又、上記ポリオキシアルキレン基としては、ポリオキシ
エチレン基、ポリオキシプロピレン基、ポリオキシブチ
レン基及びこれらの構成モノマーが共重合されたもの等
をあげることができるが、ポリオキシエチレン部を少な
くともポリオキシアルキレンに対して40重量%以上含
有する必要がある。これ未満にあっては、十分な親水性
が得られなくなり好ましくない。Examples of the polyoxyalkylene groups include polyoxyethylene groups, polyoxypropylene groups, polyoxybutylene groups, and copolymerized monomers of these. The content must be 40% by weight or more based on the oxyalkylene. If it is less than this, sufficient hydrophilicity cannot be obtained, which is not preferable.
また、上記変性シリコンの分子量は、i、ooo〜io
o、 oooとする必要があり、この範囲をはずれると
親水性が低下し、特、に1.000未満の場合にこの傾
向が著しい。Further, the molecular weight of the modified silicon is i, ooo to io
o, ooo, and if it is out of this range, the hydrophilicity decreases, and this tendency is particularly noticeable when it is less than 1.000.
本発明においては、以上に述べたポリオキシアルキレン
変性シリコンを、極めて少量の5〜20重量%、好まし
くは5〜15重量%配合した処理剤を使用することが重
要である。この配合量が20重量%を越える場合にあっ
ては、耐久性に優れた親水性を呈するものの、製綿工程
、不織布製造工程等でのスカム発生が多くなり、かつ製
綿時の捲縮付与工程の安定性及びスライバー製造時の工
程安定性(不織布目付斑の要因〉が低下する傾向にあり
好ましくない。さらには、接着障害が発生して不織布の
接着強度が低下したり、あるいは静電気発生の抑制効果
が不十分でカード通過性が損なわれる場合もある。一方
、5重量%未満の場合では、水洗耐久性のある親水性は
得られなくなる9本発明においては、上記ポリオキシア
ルキレン変性シリコンの外に、下記特定の〈ポリオキシ
アルキレン〉アルキル燐酸エステルアルカリ金属塩(B
成分)を併用することが肝要であり、かくすることによ
って水洗耐久性の優れた親水性を損なうことなく、前記
工程安定性及び不織布の品質を著しく改善できるのであ
る。In the present invention, it is important to use a processing agent containing a very small amount of 5 to 20% by weight, preferably 5 to 15% by weight of the polyoxyalkylene-modified silicone described above. If the blending amount exceeds 20% by weight, although it exhibits excellent durability and hydrophilicity, scum will be generated in the cotton manufacturing process, nonwoven fabric manufacturing process, etc., and crimping will occur during cotton manufacturing. This is undesirable as it tends to reduce the process stability and the process stability during sliver production (the cause of non-woven fabric unevenness).Furthermore, adhesion failure may occur and the adhesive strength of the non-woven fabric may decrease, or static electricity may be generated. In some cases, the suppressing effect is insufficient and the card passage property is impaired.On the other hand, if the amount is less than 5% by weight, hydrophilicity with water washing durability cannot be obtained9. In addition, the following specific <polyoxyalkylene> alkyl phosphate ester alkali metal salt (B
It is important to use these components in combination, and by doing so, the process stability and quality of the nonwoven fabric can be significantly improved without impairing the hydrophilicity, which has excellent water washing durability.
本発明で用いる(ポリオキシアルキレン)アルキル燐酸
エステルアルカリ金属塩におけるアルキル基の平均炭素
数は極めて重要であり、8〜10、好ましくは8とする
必要がある。該平均炭素数が8未満の場合にあっては、
界面活性の能力が低下して処理剤の安定性が低下し、一
方10を越える場合には十分な親水性が得られなくなる
とともに、処理剤の粘着性が増大する傾向があり、カー
ドへの捲付き、あるいはヒートローラーへの捲付き等の
トラブルを生ずるため好ましくない。The average carbon number of the alkyl group in the (polyoxyalkylene)alkyl phosphate ester alkali metal salt used in the present invention is extremely important and needs to be 8 to 10, preferably 8. If the average carbon number is less than 8,
The surfactant ability decreases and the stability of the processing agent decreases, while if it exceeds 10, sufficient hydrophilicity cannot be obtained and the tackiness of the processing agent tends to increase, making it difficult to wind the card. This is not preferable because it may cause problems such as sticking or winding around the heat roller.
また、ポリオキシエチレンアルキル基中のポリオキシエ
チレン基の平均重合度はO〜15、好ましくは0〜5(
重合度が0の時は単なるアルキル基であることを示す〉
とする必要がある。重合度が15を越えると、親水性が
低下するとともに静電気の発生が大きくなって、カード
工程通過性が低下する傾向にあるため好ましくない。In addition, the average degree of polymerization of the polyoxyethylene group in the polyoxyethylene alkyl group is 0 to 15, preferably 0 to 5 (
When the degree of polymerization is 0, it shows that it is a simple alkyl group〉
It is necessary to do so. If the degree of polymerization exceeds 15, the hydrophilicity decreases and the generation of static electricity increases, which tends to reduce the ability to pass through the carding process, which is not preferable.
また、燐酸化度は0.5〜1.0とする必要がある。Moreover, the degree of phosphorylation needs to be 0.5 to 1.0.
この値が0.5未満ではスカムが多発するようになり、
かつまた集束性も低下して、製綿工程、不織布製造工程
の安定性が損なわれるようになる。その結果、得られる
不織布は日付斑等の品質が不十分なものとなる。また、
未反応のアルコールが多くなるため、臭気が強く、生産
上好ましくないという欠点もある。一方、燐酸化度が1
.0を越える場合には、界面活性剤としての性能が損な
われ、。If this value is less than 0.5, scum will occur frequently,
Moreover, the cohesiveness is also reduced, and the stability of the cotton manufacturing process and the nonwoven fabric manufacturing process is impaired. As a result, the obtained nonwoven fabric has insufficient quality such as date spots. Also,
It also has the disadvantage that it has a strong odor, which is unfavorable in terms of production, since there is a large amount of unreacted alcohol. On the other hand, the degree of phosphorylation is 1
.. When it exceeds 0, the performance as a surfactant is impaired.
前記A成分との相溶性が低下するため、処理剤を熱接着
性繊維の表面に均一に付着できなくなる。Since the compatibility with the component A decreases, the treatment agent cannot be uniformly attached to the surface of the heat-adhesive fiber.
その結果、得られる親水性は不安定なものとなり、かつ
その水洗耐久性は著しく劣ったものとなり好ましくない
。なお、本発明において燐酸化度とは、使用した(オキ
シエチレン付加〉アルコールに燐原子が何モル結合して
いるかを算出した値であり、平均的にはこの値が1の時
リン酸モノエステルを、また0、5の時リン酸ジエステ
ルを示す(燐原子の定量は燐モリブデン酸比色法による
)。As a result, the obtained hydrophilicity becomes unstable and the water washing durability becomes extremely poor, which is not preferable. In addition, in the present invention, the degree of phosphorylation is a value calculated by calculating how many moles of phosphorus atoms are bonded to the (oxyethylene addition) alcohol used, and on average, when this value is 1, the phosphoric acid monoester , and when it is 0 or 5, it indicates a phosphoric acid diester (phosphorus atoms are determined by the phosphomolybdic acid colorimetric method).
また、アルカリ金属化合物による中和度も工程安定性に
大きく影響を及ぼし、酸価が150を越えると耐熱性が
低下してスカムの発生が多くなり、かつ溶解性も不良と
なり、臭気発生の原因ともなる。したがって、酸価は0
〜150の範囲で低い程好ましいが、あまりに低くなり
すぎるとA成分との相溶性が低下する傾向にあるので、
好ましくは10〜100の範囲とするのが望ましい。な
お、アルカリ金属としては、ナトリウム、カリウム、リ
チウム等をあげることができるが、就中カリウムが好ま
しく用いられる。In addition, the degree of neutralization by an alkali metal compound has a large effect on process stability, and when the acid value exceeds 150, heat resistance decreases and scum formation increases, and solubility becomes poor, causing odor generation. It also becomes. Therefore, the acid value is 0
The lower it is in the range of ~150, the more preferable it is, but if it becomes too low, the compatibility with component A tends to decrease.
Preferably, it is in the range of 10 to 100. Incidentally, examples of the alkali metal include sodium, potassium, lithium, etc., and among them, potassium is preferably used.
このように、(ポリオキシアルキレン)アルキル燐酸エ
ステル塩の性質は重要であって、アルキル基の炭素数、
オキシアルキレンの付加モル数、燐酸化度及び酸価を適
正な範囲内としたものを用いて、初めて本発明の目的を
達成することができるのである。In this way, the properties of the (polyoxyalkylene)alkyl phosphate ester salt are important, including the number of carbon atoms in the alkyl group,
The object of the present invention can only be achieved by using a material in which the number of moles of oxyalkylene added, the degree of phosphorylation, and the acid value are within appropriate ranges.
本発明においては、上記(ポリオキシエチレン〉アルキ
ル燐酸エステルアルカリ金属塩1種または2種以上を2
5〜95重量%、好ましくは40〜95重量%配合した
処理剤を用いる必要がある。この配合量が25重量%未
滴化あ)ては、前記A成分との併用効果が低減し、工程
安定性が悪化するとともに、親水性及び耐久性が低下す
る。なお、上記B成分として、アルカリ燐酸エステル塩
とポリオキシエチレンアルキル燐酸エステル塩を併用す
るのが好ましく、特に混合比を1=3〜3:1とするの
が望ましい。かくすることにより、水洗耐久性に優れf
SM4水性付与と、工程安定性及び不織布の品質改善を
同時に解決するといった本願の目的を高度に達成できる
。In the present invention, two or more of the above (polyoxyethylene>alkyl phosphate ester alkali metal salts)
It is necessary to use a processing agent containing 5 to 95% by weight, preferably 40 to 95% by weight. If this amount is less than 25% by weight, the effect of the combination with component A is reduced, process stability is deteriorated, and hydrophilicity and durability are reduced. As the component B, it is preferable to use an alkali phosphate salt and a polyoxyethylene alkyl phosphate salt in combination, and it is particularly desirable that the mixing ratio be 1=3 to 3:1. By doing so, it has excellent water washing durability.
The purpose of the present application, which is to simultaneously provide SM4 with aqueous properties and improve process stability and quality of nonwoven fabrics, can be highly achieved.
以上に述べた本発明で用いる処理剤には、本発明の効果
を損なわない範囲内で他の刑、例えば、ノニオン性界面
活性剤、前記B成分以外のアニオン活性剤、帯電防止剤
、増白剤、酸化防止剤、紫外線吸収剤、染料、顔料等を
添加することもできる。The processing agent used in the present invention described above may contain other additives within the range that does not impair the effects of the present invention, such as nonionic surfactants, anionic surfactants other than component B, antistatic agents, whitening agents, etc. Agents, antioxidants, ultraviolet absorbers, dyes, pigments, etc. can also be added.
本発明の熱接着性繊維は、繊維に対し前記処理剤を0.
05〜5重量%、好ましくは0.3〜1.0重量%付着
させる。付着量が0゜05重量%未満の場合には、十分
な親水性は得られず、かつ潤滑性と集束性も不十分なも
のとなってカード工程等でのトラブル発生の要因となる
。一方、5重量%を越えるとスカム発生やローラー捲付
きの傾向は大きくなり、また接着強力も低下する傾向に
ある。The heat-adhesive fiber of the present invention is prepared by applying the above-mentioned treatment agent to the fiber at 0.00%.
05 to 5% by weight, preferably 0.3 to 1.0% by weight. If the amount of adhesion is less than 0.05% by weight, sufficient hydrophilicity will not be obtained, and the lubricity and cohesiveness will also be insufficient, leading to troubles in the carding process, etc. On the other hand, if it exceeds 5% by weight, there is a tendency for scum generation and roller rolling to increase, and adhesive strength also tends to decrease.
処理剤を付着させるには、水洗エマルジョンなどとして
、紡糸及び延伸工程において浸漬またはスプレ一方式等
通常の方法をそのまま適用すればよい。To attach the treatment agent, a conventional method such as dipping or spraying in the spinning and stretching steps may be applied as a water-washed emulsion.
本発明で前記処理剤を付着せしめる熱接着性繊維は、融
点く非品性重合体にあってはその軟化点〉が50〜20
0℃の熱可塑性重合体を熱接着性成分とし、かつその少
なくとも50重量%がポリオレフィン系重合体であるこ
とが重要である。前記処理剤、特に変性シリコンはポリ
オレフィン系重合体との親和性が特異的に高いため、接
着性成分の50重量%以上がポリオレフィン系重合体の
時、前記処理剤が極めて強固に熱接着性繊維表面に固着
され、その結果水洗耐久性に優れた親水性が得られると
同時に、スカムの発生が低減されるものと推定される。In the present invention, the heat-adhesive fiber to which the treatment agent is attached is a non-polymer with a softening point of 50 to 20.
It is important that the thermoadhesive component is a thermoplastic polymer at 0° C., and that at least 50% by weight thereof is a polyolefin polymer. The processing agent, especially the modified silicone, has a specific high affinity with polyolefin polymers, so when 50% by weight or more of the adhesive component is polyolefin polymer, the processing agent can extremely firmly bond the thermal adhesive fibers. It is presumed that it is fixed to the surface, resulting in hydrophilicity with excellent washing durability, and at the same time, the generation of scum is reduced.
なお、上記熱接着性繊維は、接着性成分単独からなる繊
維であってもよく、また他の繊維形成性重合体との複合
繊維(芯鞘型、サイドバイサイド型等〉であってもよい
。また、断面形状も、丸断面、偏平、T型、Y型、中型
、異形等の多葉異形断面、中空断面、異形中空断面等い
ずれの形態にしてもよい。特に中空率が3〜40%の中
空部を有するものは、不織布の電性を向上させる。The heat-adhesive fiber may be a fiber consisting of an adhesive component alone, or may be a composite fiber (core-sheath type, side-by-side type, etc.) with another fiber-forming polymer. The cross-sectional shape may be any form such as a round cross-section, a flattened cross-section, a T-shape, a Y-shape, a medium shape, a multi-lobed irregular cross-section such as an irregular shape, a hollow cross-section, and an irregular hollow cross-section. Those having hollow portions improve the electrical properties of the nonwoven fabric.
次に、接着性成分として好ましく用いられるポリオレフ
ィン系重合体としては、例えばポリエチレン、ポリプロ
ピレン、ポリブテン−1、ポリペンテン−1及びこれら
のランダムもしくはブロック共重合体、あるいは、さら
にメタクリル酸、アクリル酸、マレイン酸、フマル酸、
クロトン酸、イタコン酸等の不飽和カルボン酸、および
それらのエステル、酸無水物などの誘導体から選択され
る少なくとも1種以上を共重合したポリオレフィン系重
合体〈変性オレフィンと称す〉をあげることができ、さ
らには前記ポリオレフィン系重合体に前記不飽和カルボ
ン酸又はその誘導体の少くとも1種をグラフトしたグラ
フト重合体をあげることができる。中でも製綿時の工程
安定性及び不織布の風合〈柔軟性〉等の面から不飽和カ
ルボン酸1種以上とエチレン、プロピレン、ブテン−1
等のα−オレフィンの少なくとも1種を共重合した変性
ポリオレフィンが好ましい。Next, polyolefin polymers preferably used as adhesive components include, for example, polyethylene, polypropylene, polybutene-1, polypentene-1, and random or block copolymers thereof, or methacrylic acid, acrylic acid, and maleic acid. , fumaric acid,
Examples include polyolefin polymers (referred to as modified olefins) that are copolymerized with at least one selected from unsaturated carboxylic acids such as crotonic acid and itaconic acid, and derivatives such as esters and acid anhydrides thereof. Further examples include graft polymers in which at least one of the unsaturated carboxylic acids or derivatives thereof is grafted onto the polyolefin polymer. Among them, one or more unsaturated carboxylic acids and ethylene, propylene, butene-1 are used from the viewpoint of process stability during cotton manufacturing and the texture (flexibility) of nonwoven fabrics.
Modified polyolefins copolymerized with at least one kind of α-olefins such as the following are preferred.
ポリオレフィン系重合体以外の熱接着性成分としては、
前述の如く融点が50〜200℃の範囲にあれば特に限
定する必要はなく、ポリ酢酸ビニル、ポリアクリル酸エ
ステル、あるいはこれらの共重合体、ナイロン10、ナ
イロン12の如きポリアミド、あるいは共重合ポリアミ
ド、ポリエステルもしくは共重合ポリエステル等をあげ
ることができ、特に90〜150℃の融点を有するもの
が好ましい。Thermal adhesive components other than polyolefin polymers include:
As mentioned above, there is no particular limitation as long as the melting point is in the range of 50 to 200°C, and polyvinyl acetate, polyacrylic acid ester, or copolymers thereof, polyamides such as nylon 10 and nylon 12, or copolymerized polyamides may be used. , polyester, copolyester, etc., and those having a melting point of 90 to 150°C are particularly preferred.
一方、複合繊維を構成する際の他の繊維形成性重合体と
しては、融点が150℃以上でかつ熱接着性成分より融
点の高い熱可塑性ポリマー、例えばPET、PBT、ナ
イロン−6、ナイロン−66、ポリプロピレン等をあげ
ることができ、特に最終的に得られる不織布の嵩高性、
耐ヘタリ性、弾力性、ソフトな風合の面でPETもしく
はPBTが好ましい。なお、複合繊維断面の全周長に対
する上記繊維形成重合体が占める割合、すなわち繊維断
面周率は60%以下(熱接着成分が占める割合は40%
以上〉とするのが好ましく、また繊維形成性重合体と熱
接着成分との間に親和性が不足して、界面剥離が発生し
易い場合には、40重量%以下の割合で熱接着性成分も
しくはこれと親和性の高い重合体を繊維形成性重合体に
配合するのが接着強力向上の面で好ましい。On the other hand, as other fiber-forming polymers for forming composite fibers, thermoplastic polymers having a melting point of 150° C. or higher and higher than that of the thermoadhesive component, such as PET, PBT, nylon-6, nylon-66, etc. , polypropylene, etc., especially the bulkiness of the final nonwoven fabric,
PET or PBT is preferable in terms of resistance to set, elasticity, and soft texture. The ratio of the fiber-forming polymer to the total circumference of the composite fiber cross section, that is, the fiber cross-sectional circumference is 60% or less (the ratio of the thermal adhesive component is 40%).
If the affinity between the fiber-forming polymer and the heat-adhesive component is insufficient and interfacial peeling is likely to occur, the heat-adhesive component should preferably be Alternatively, it is preferable to blend a polymer having high affinity with the fiber-forming polymer with the fiber-forming polymer in order to improve adhesive strength.
以上に詳述した本発明の熱接着性繊維は、不織布製造時
のカード通過性、抄紙性等の観点より、その繊度を0.
1〜20デニールとするのが望ましい。The thermoadhesive fiber of the present invention described in detail above has a fineness of 0.0000.000.
It is desirable to set it as 1-20 deniers.
繊維長、捲縮数は、用途によって異なり、例えば抄紙用
では夫々35mn+以下、0〜10ケ/25mm、また
乾式不織布用には、20〜150mm、6〜25ケ/2
5mmで、さらに、捲縮度、捲縮弾性度(JIS L
1015)及び熱収縮率(80℃〉が夫々8%以上、7
0%以上及び10%以下のものが適している。The fiber length and number of crimps vary depending on the application, for example, for paper making, 35 mm+ or less, 0 to 10 strands/25 mm, and for dry nonwoven fabric, 20 to 150 mm, 6 to 25 strands/2.
At 5 mm, the crimp degree and crimp elasticity (JIS L
1015) and heat shrinkage rate (80℃> are respectively 8% or more, 7
0% or more and 10% or less are suitable.
本発明の熱接着性繊維は、これ単独で不織布となしても
よく、また通常の繊維、例えばポリエステル短繊維、ポ
リプロピレン短繊維等と混合して用いてもよく、用途に
合わせて適宜選択することができる。The heat-adhesive fiber of the present invention may be used alone as a nonwoven fabric, or may be used in combination with ordinary fibers such as polyester short fibers, polypropylene short fibers, etc., and may be selected as appropriate depending on the purpose. I can do it.
(発明の作用・効果〉
本発明の熱接着性繊維は、処理剤と接着性成分の親和性
が良好なので、水洗耐久性に優れた親水性を呈する。し
かも、極めて特定のリン酸エステル塩と組み合わせて使
用することにより、親水性を低減させることなくポリオ
キシアルキレン変性シリコンの使用量を極めて少量とす
ることができるので、製綿工程、不織布製造工程等での
スカム発生及び不織布の品質斑(日付斑)を著しく改善
できる。(Actions and Effects of the Invention) The heat-adhesive fiber of the present invention has good affinity with the treatment agent and the adhesive component, so it exhibits hydrophilicity with excellent water washing durability. When used in combination, the amount of polyoxyalkylene-modified silicone used can be reduced to an extremely small amount without reducing hydrophilicity, thereby reducing the occurrence of scum in the cotton manufacturing process, nonwoven fabric manufacturing process, etc. and the quality unevenness of nonwoven fabrics ( Date spots) can be significantly improved.
さらには、上記リン酸エステル塩と変性シリコンとの相
溶性は極めて良好で、処理剤の均一付着が得られ、安定
した親水性の水洗耐久性及び優れた工程通過性が達成で
きる。Furthermore, the compatibility between the phosphoric acid ester salt and the modified silicone is extremely good, and uniform adhesion of the treatment agent can be obtained, and stable hydrophilic water washing durability and excellent process passability can be achieved.
本発明の熱接着性繊維は、上述の通り耐久性のある親水
性が付与されているので、ティーバッグ。As mentioned above, the thermoadhesive fiber of the present invention has durable hydrophilic properties, so it can be used in tea bags.
化粧用パフ、ウェットティッシュ等の食品家庭用、生理
ナプキン及び紙オムツ等の表面材、オムツライナー、湿
布基布等の衛生医療用の不織布に好適に用いることがで
きる。また、製綿工程、不織布製造工程等でのスカム発
生等のトラブル発生が著しく低減されており、品質の良
好な不織布が生産性よく得られるので、その工業的意義
は極めて大である。It can be suitably used for nonwoven fabrics for food and household use such as cosmetic puffs and wet tissues, surface materials for sanitary napkins and paper diapers, and hygiene and medical use such as diaper liners and poultice base fabrics. In addition, the occurrence of troubles such as scum generation in the cotton manufacturing process, nonwoven fabric manufacturing process, etc. is significantly reduced, and nonwoven fabrics of good quality can be obtained with high productivity, so its industrial significance is extremely large.
〈実施例〉
以下、実施例により本発明を更に具体的に説明する。な
お、各物性の評価は下記の方法にしたがった。<Examples> The present invention will now be described in more detail with reference to Examples. In addition, evaluation of each physical property followed the following method.
(1)処理剤溶液安定性
濃度10%の水溶液を作成し、20℃で3日間放置後の
液の状n(沈澱、層分離等)で判定した。(1) Stability of processing agent solution An aqueous solution with a concentration of 10% was prepared and evaluated based on the state of the liquid (precipitation, layer separation, etc.) after being left at 20° C. for 3 days.
(2)押込捲縮機通過性
押込捲縮機にて捲縮を付与する際、押込捲縮機が正常に
運転できかつ良好な捲縮が付与できる場合を良好(○)
、押込捲縮機がガタッキ等で正常に運転できずまた斑の
大きな捲縮しか付与できない場合を不良(×〉、両者の
中間でなんとか運転可能な場合をほぼ良好(△〉で評価
した。(2) Passability through the push crimper When applying crimps with the push crimper, the case where the push crimper can operate normally and provide good crimp is rated as good (○).
A case in which the push-in crimper could not be operated normally due to looseness or the like and only crimps with large spots could be applied was evaluated as poor (×>), and a case in which it could be operated somehow between the two was evaluated as almost good (△>).
(3)親水性
繊維1.Ogを採取し、直径的4cmの球状繊維塊をつ
くり、水10100Oを入れたビーカーの水面上方5c
mの高さから繊維塊を自然落下させ、繊維塊が水面下に
沈むまでの浸漬時間を測定して親水性の大小を評価した
。(3) Hydrophilic fiber 1. Collect Og, make a spherical fiber mass with a diameter of 4 cm, and place it 5 cm above the water surface in a beaker containing 10,100 O of water.
The fiber mass was allowed to fall naturally from a height of m, and the immersion time until the fiber mass sank below the water surface was measured to evaluate the hydrophilicity.
(4)親水性の水洗耐久性
水面下に浸漬した繊維塊を取り出し遠心分離機で脱水乾
燥した後、再度上記の親水性評価方法で浸漬時間を測定
した。(4) Durability of hydrophilic water washing After the fiber mass immersed under water was taken out and dehydrated and dried using a centrifuge, the immersion time was measured again using the above-mentioned hydrophilicity evaluation method.
浸漬時間が60秒を超えるまで繰り返し、浸漬時間が6
0秒以下を維持した浸漬回数をもって、浸水性能の水洗
に対する耐久性とした。Repeat until the soaking time exceeds 60 seconds, and the soaking time exceeds 60 seconds.
The number of immersion times during which the immersion time was maintained at 0 seconds or less was determined as the durability against water washing of water immersion performance.
(5)スカム発生
25℃×65%RHの条件下で原綿50Kgをローラー
カードにかけ、30g/lr?目イ寸のウェブを30m
/分で紡出した際のスカム発生有無により評価した。ス
カム発生なし、を良好くO)、スカムが発生しカーデイ
ングが不能になった場合を不良(×)、両者の中間でき
りぎりカーデイング可能な場合をほぼ良好(Δ)とした
。(5) Scum generation 50 kg of raw cotton was applied to a roller card under the conditions of 25°C x 65% RH, and 30 g/lr? 30m of eye-sized web
Evaluation was made based on the presence or absence of scum during spinning at a speed of /min. No scum occurred, which was considered good (O), cases where scum occurred and carding was impossible were judged poor (x), and cases where carding was barely possible between the two were judged good (Δ).
(6)静電気発生
25°C×65%RHの条件下で原綿50Kgをローラ
ーカードにかけ、30g/rr?′目付のウェブを30
m/分で紡出した際の静電気発生有無により評価した。(6) Static electricity generation 50 kg of raw cotton was applied to a roller card under the conditions of 25°C x 65% RH, and 30 g/rr? 'The web with a weight of 30
Evaluation was made based on whether or not static electricity was generated during spinning at m/min.
静電気発生なしを良好(O)、静電気が発生しカーデ
イングが不能になった場合を不良(×)、両者の中間で
きりぎりカーデイング可能な場合をほぼ良好(Δ)とし
た。A case where static electricity was not generated was judged as good (O), a case where static electricity was generated and carding was impossible was judged as poor (x), and a case where carding was possible as much as possible between the two was judged as good (Δ).
(7)カード捲付き
25℃×65%RH条件下でローラーカードを用いて3
0g/rrrの目付のウェブを30m/分で紡出した際
、正常に運転できたものを良好(○〉、カードの針布へ
の捲付きが多発して運転できなかったものを不良く×〉
、両者の中間でなんとか運転できたものを中間(Δ〉で
判定した。(7) Using a roller card under 25℃ x 65%RH conditions with card winding
When spinning a web with a basis weight of 0 g/rrr at 30 m/min, those that could be operated normally were rated Good (○), and those that could not be operated due to frequent winding of the card on the clothing were rated Bad ×. 〉
, and those that managed to operate between the two were judged as intermediate (Δ〉).
(8)不織布の日付斑
目付30g/−のウェブを165°C下20秒熱処理し
て不織布を作成する。この不織布から10cmx10c
mの試験片を100枚切り収ってその重量を測定し、そ
れらの測定値のσ値より判定した。(8) A web of nonwoven fabric having a grain size of 30 g/- is heat treated at 165°C for 20 seconds to produce a nonwoven fabric. 10cm x 10cm from this non-woven fabric
100 test pieces of size m were cut and weighed, and the weight was determined based on the σ value of the measured values.
σ値が0.003未満を良好(○〉、σ値が0、003
〜0.006をほぼ良好(Δ)、σ値が0、006を超
える場合を不良(×)で表示した。σ value less than 0.003 is good (○>, σ value is 0, 003
~0.006 was indicated as almost good (Δ), and a case where the σ value exceeded 0.006 was indicated as poor (×).
(9)接着強度
前記と同様にして作成した不織布から、マシン方向に巾
6cm、長さ20cmの試験片を切り取り、つかみ間隔
10cm、伸長速度20cm/分で引張破断強力を測定
した。(9) Adhesive Strength A test piece with a width of 6 cm and a length of 20 cm was cut in the machine direction from the nonwoven fabric prepared in the same manner as above, and the tensile strength at break was measured at a gripping interval of 10 cm and an elongation rate of 20 cm/min.
接着強度は引張破断強力を試験片重量で除した値とした
。The adhesive strength was determined by dividing the tensile strength at break by the weight of the test piece.
((0)臭気
ウェブを140℃×1分熱処理した際、臭いの感じられ
なかったものを良好(O〉、臭気が強く不快感をもよお
すものを不良(×〉、両者の中間をほぼ良好く△)で評
価した。((0) When the odor web was heat-treated at 140°C for 1 minute, those with no odor were evaluated as good (O), those with a strong odor that caused discomfort were evaluated as poor (×), and those in between the two were evaluated as good. It was evaluated as △).
実施例1
芯成分として極限粘度0.64のポリエチレンテレフタ
レート〈融点260℃〉を用い、鞘成分として高密度ポ
リエチレン(i!点130℃〉80部及びエチレン/メ
チルメタクリレート/無水マレイン酸共重合体く共重合
モル比90/6/4、メルトインデックス8、融点95
℃〉20部からなる熱接着性成分を用い、孔数210を
有する芯鞘型複合紡糸口金より、紡糸温度280℃、紡
糸速度1000 m/分、複合比50150 (重量比
〉で紡糸した。次いで得られた未延伸糸を集めて200
万デニールのトウにした後、80°Cの温水中にて3.
0倍に延伸し、表−1及び2に示す各種の処理剤(10
%水性エマルジョン)を表−3〜4に示す付着率(有効
成分として〉で付与した。この延伸糸を押込捲縮機に供
給して捲縮を付与した後、100℃で弛緩熱処理を施し
51mmの繊維長に切断して、単繊維繊度3.0デニー
ル、捲縮数15ケ/25mm、捲縮度12%、捲縮弾性
度77%、80℃乾熱収縮率1%以下の熱接着性繊維を
得た。Example 1 Polyethylene terephthalate (melting point 260°C) with an intrinsic viscosity of 0.64 was used as the core component, 80 parts of high-density polyethylene (i! point 130°C) and ethylene/methyl methacrylate/maleic anhydride copolymer were used as the sheath component. Copolymerization molar ratio 90/6/4, melt index 8, melting point 95
Using a heat-adhesive component consisting of 20 parts of a heat-adhesive component having 210 holes, the material was spun at a spinning temperature of 280°C, a spinning speed of 1000 m/min, and a composite ratio of 50150 (weight ratio). Collect the obtained undrawn yarn and
After forming tow of 10,000 denier, 3.
Stretched to 0 times, various processing agents shown in Tables 1 and 2 (10
% aqueous emulsion) was applied at the adhesion rate (as the active ingredient) shown in Tables 3 and 4. After this drawn yarn was fed to a push crimper and crimped, it was subjected to relaxation heat treatment at 100°C to form a 51 mm When cut to a fiber length of Obtained fiber.
これらの熱接着性繊維を用いて、前記評価方法にしたが
って評価した結果を表−3〜4に示す。Tables 3 and 4 show the results of evaluation using these heat-adhesive fibers according to the evaluation method described above.
なお、接着強度は、熱接着性繊維単独で不織布となした
場合のものである。Note that the adhesive strength is the one when the nonwoven fabric is made of heat-adhesive fiber alone.
実施例2
鞘成分として表−5に記載の熱接着性成分を用いる以外
は実施例1と同様にして熱接着性繊維を得た。〈阻し、
処理剤は表−1記載の■を使用し、1寸着量は0.5w
t%とした。)
得られた熱接着性繊維を実施例1と同様にし評価した。Example 2 A thermoadhesive fiber was obtained in the same manner as in Example 1 except that the thermoadhesive component listed in Table 5 was used as the sheath component. <obstruction,
For the treatment agent, use ■ listed in Table 1, and the amount per inch is 0.5w.
It was set as t%. ) The obtained thermal adhesive fibers were evaluated in the same manner as in Example 1.
その結果を表−6に示す。The results are shown in Table-6.
t
MA
MAΩ
A
A
MG
G
:エチレン、
:メチルメタクリレート、
:無水マレイン酸、
:テレフタル酸、
:イソフタル酸、
:ヘキサメチレングリコール
:エチレングリコール
表
6
ネ
:比較例
実施(Ijlj3
融点130°Cの高密度ポリエチレンを溶融温度250
℃で溶融した後、孔数210孔を有する口金を用いて紡
糸速度800m/分で紡糸し、延伸温度80°Cで2.
5倍に延伸した。次いで、表−7に記載の処理剤(10
%水性エマルジョン〉を付着率0.5wt%(有効成分
として〉となるように付与した後、押込捲縮機で捲縮を
吋与し、次いでioo’cで弛緩熱処理して熟接着性繊
維を得た。t MA MAΩ AA MG G : Ethylene, : Methyl methacrylate, : Maleic anhydride, : Terephthalic acid, : Isophthalic acid, : Hexamethylene glycol : Ethylene glycol Table 6 Ne: Comparative example implementation (Ijlj3 High density with melting point of 130°C Polyethylene melting temperature 250
After melting at ℃, spinning was carried out at a spinning speed of 800 m/min using a die having 210 holes, and the drawing temperature was 80 ℃.
It was stretched 5 times. Next, the processing agent (10
% aqueous emulsion> was applied at a deposition rate of 0.5 wt% (as the active ingredient), crimped with a push crimper, and then subjected to relaxation heat treatment with IOO'C to form fully adhesive fibers. Obtained.
前記評価方法にしたがって評価した結果を表−7に示す
。なお、ウェブを作成する際には、通常のポリエチレ〉
・テレフタレート短繊維(単糸繊度3.0デニール、繊
維長51mm )と50150の割合で混合して評価し
た。Table 7 shows the results of evaluation according to the above evaluation method. In addition, when creating the web, use regular polyethylene
- It was evaluated by mixing it with terephthalate short fibers (single filament fineness 3.0 denier, fiber length 51 mm) at a ratio of 50,150.
Claims (1)
し、かつその少なくとも50重量%がポリオレフィン系
重合体である熱接着性繊維において、該繊維表面に下記
(A)及び(B)成分を含有する処理剤が、処理剤有効
成分として0.05〜5重量%付着していることを特徴
とする熱接着性繊維。 (A)シリコン含有率が50%以下、ポリオキシアルキ
レン中のポリオキシエチレン含有率が40%以上で、分
子量が1,000〜100,000のポリオキシアルキ
レン変性シリコン:5〜20重量%(B)平均炭素数が
8〜10のアルキル基であってオキシエチレン付加モル
数が0〜15の(ポリオキシエチレン)アルキル基で、
燐酸化度が 0.5〜1.0、酸価が0〜150の、(ポリオキシエ
チレン)アルキル燐酸エステルのアルカリ金属塩:25
〜95重量%[Scope of Claims] A thermoadhesive fiber whose thermoadhesive component is a thermoplastic polymer having a melting point of 50 to 200°C, and at least 50% by weight of which is a polyolefin polymer, the fiber surface having the following (A): A heat-adhesive fiber characterized in that a processing agent containing component (B) is attached in an amount of 0.05 to 5% by weight as an active ingredient of the processing agent. (A) Polyoxyalkylene-modified silicone with a silicon content of 50% or less, a polyoxyethylene content in polyoxyalkylene of 40% or more, and a molecular weight of 1,000 to 100,000: 5 to 20% by weight (B ) an alkyl group having an average carbon number of 8 to 10 and a (polyoxyethylene) alkyl group having an added mole of oxyethylene of 0 to 15;
Alkali metal salt of (polyoxyethylene) alkyl phosphoric acid ester having a degree of phosphorylation of 0.5 to 1.0 and an acid value of 0 to 150: 25
~95% by weight
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1192490A JPH0359169A (en) | 1989-07-27 | 1989-07-27 | Hot-weldable fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1192490A JPH0359169A (en) | 1989-07-27 | 1989-07-27 | Hot-weldable fiber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0359169A true JPH0359169A (en) | 1991-03-14 |
Family
ID=16292172
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1192490A Pending JPH0359169A (en) | 1989-07-27 | 1989-07-27 | Hot-weldable fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0359169A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5654086A (en) * | 1995-08-01 | 1997-08-05 | Chisso Corporation | Durable hydrophilic fibers, cloth articles and molded articles |
| US6211101B1 (en) | 1998-07-10 | 2001-04-03 | Chisso Corporation | Durable hydrophilic fiber and fabric using the same |
| WO2024053624A1 (en) * | 2022-09-06 | 2024-03-14 | 竹本油脂株式会社 | Hydrophilization agent, nonwoven fabric, and method for producing nonwoven fabric |
| WO2025182765A1 (en) * | 2024-02-29 | 2025-09-04 | 松本油脂製薬株式会社 | Water permeability-imparting agent and use thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63303184A (en) * | 1987-05-29 | 1988-12-09 | 松本油脂製薬株式会社 | Binder fiber treatment agent |
| JPS6420378A (en) * | 1987-07-09 | 1989-01-24 | Kuraray Co | Hydrophylicity imparting agent suitable for polyolefinic fiber |
-
1989
- 1989-07-27 JP JP1192490A patent/JPH0359169A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63303184A (en) * | 1987-05-29 | 1988-12-09 | 松本油脂製薬株式会社 | Binder fiber treatment agent |
| JPS6420378A (en) * | 1987-07-09 | 1989-01-24 | Kuraray Co | Hydrophylicity imparting agent suitable for polyolefinic fiber |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5654086A (en) * | 1995-08-01 | 1997-08-05 | Chisso Corporation | Durable hydrophilic fibers, cloth articles and molded articles |
| US6211101B1 (en) | 1998-07-10 | 2001-04-03 | Chisso Corporation | Durable hydrophilic fiber and fabric using the same |
| WO2024053624A1 (en) * | 2022-09-06 | 2024-03-14 | 竹本油脂株式会社 | Hydrophilization agent, nonwoven fabric, and method for producing nonwoven fabric |
| JP2024037140A (en) * | 2022-09-06 | 2024-03-18 | 竹本油脂株式会社 | Hydrophilic treatment agent, nonwoven fabric, and method for producing nonwoven fabric |
| JP2024036874A (en) * | 2022-09-06 | 2024-03-18 | 竹本油脂株式会社 | Hydrophilic treatment agent, nonwoven fabric, and method for producing nonwoven fabric |
| WO2025182765A1 (en) * | 2024-02-29 | 2025-09-04 | 松本油脂製薬株式会社 | Water permeability-imparting agent and use thereof |
| JP7736970B1 (en) * | 2024-02-29 | 2025-09-09 | 松本油脂製薬株式会社 | Water permeability agents and their uses |
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