JP2013170340A - Fiber for air-laid nonwoven fabric and air-laid nonwoven fabric using the fiber - Google Patents

Fiber for air-laid nonwoven fabric and air-laid nonwoven fabric using the fiber Download PDF

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JP2013170340A
JP2013170340A JP2012036883A JP2012036883A JP2013170340A JP 2013170340 A JP2013170340 A JP 2013170340A JP 2012036883 A JP2012036883 A JP 2012036883A JP 2012036883 A JP2012036883 A JP 2012036883A JP 2013170340 A JP2013170340 A JP 2013170340A
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fiber
nonwoven fabric
air
ethylene
laid nonwoven
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Munenori Kumagai
宗訓 熊谷
Yoshinobu Omae
好信 大前
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Kuraray Co Ltd
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Kuraray Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a fiber for an air-laid nonwoven fabric capable of producing an air-laid nonwoven fabric having sufficient flexibility, liquid-retaining properties, air permeability, bulkiness, hydrophilic properties and strength as a nonwoven fabric.SOLUTION: The fiber for the air-laid nonwoven fabric comprises an ethylene-vinyl alcohol based copolymer containing 5-70 mol% of ethylene, and has a fiber length of 2-30 mm and a crimp number of 3-30 crimps/inch. The air-laid nonwoven fabric that uses at least 10 wt.% or more of the fiber is also disclosed.

Description

本発明は、エアレイド不織布用繊維に関し、更に詳しくは、エチレンービニルアルコール系共重合体からなるエアレイド不織布用繊維に関する。より好ましくは、コスメ製品用エアレイド不織布に関するものである。   The present invention relates to a fiber for an air laid nonwoven fabric, and more particularly to a fiber for an air laid nonwoven fabric made of an ethylene-vinyl alcohol copolymer. More preferably, it relates to an airlaid nonwoven fabric for cosmetic products.

エアレイド製法とは乾式不織布製造方法の1種であり、パルプや合成繊維などの短繊維を空気中で開繊させた後、ワイヤー上にウェブを形成させる方法である。そのため、シートの製造に水を使用しないことによる排水負荷の軽減や、繊維の配向がランダムになること、また、空気搬送可能な材料であれば、SAP(高吸水性樹脂)や、活性炭などの粉体なども同時に不織布内部の空隙に介在させることもできるため、多様な材料が混合した不織布を1つの工程で得ることができるなど特徴に着目され、近年特に応用分野が拡大されている製法である。
特に、吸水性能、吸油性能を有し、かつ比較的コストも安いパルプ繊維を用いたエアレイド不織布は廉価不織布としてワイパー、タオル、衛材など幅広い製品に応用されている。
The airlaid manufacturing method is one type of dry nonwoven fabric manufacturing method, in which short fibers such as pulp and synthetic fibers are opened in the air and then a web is formed on the wire. Therefore, reduction of drainage load by not using water for sheet production, random fiber orientation, and SAP (high water absorption resin), activated carbon, etc. Since powder and the like can also be intervened in the voids inside the nonwoven fabric at the same time, attention has been focused on features such as the ability to obtain a nonwoven fabric in which various materials are mixed in one step, and in recent years the method of application has been particularly expanded. is there.
In particular, air laid nonwoven fabrics using pulp fibers having water absorption performance and oil absorption performance and relatively low cost are applied to a wide range of products such as wipers, towels and hygiene materials as inexpensive nonwoven fabrics.

エアレイド不織布製造工程におけるウェブ結合方法として、現在、接着剤をスプレーして結合させるラテックスボンド法や、ポリオレフィン系もしくは、ポリエステル系の熱接着性繊維をバインダー繊維として用い融着させるサーマルボンド法、または両者を兼ね備えたマルチボンド法が使用されている(例えば特許文献1〜3等参照。)。しかし、ラテックスボンド法による結合では、不織布の空隙内へ接着剤が浸透することにより、保液性や柔軟性が低下するなどの問題を有しており、また、ポリオレフィン系やポリエステル系熱接着性繊維を用いたサーマルボンド法による結合では、これら材料に由来する疎水性により、得られた不織布の親水性、保水性、吸水性が低下するなどの問題を有している。
そのため、コスメ製品用不織布として、上記製法によるエアレイド不織布は、薬液が不織布内部まで十分に浸透せず、また柔軟性も低下するためシートを肌に触れさせた際不快感を与えるため好ましくない。
As a web bonding method in the airlaid nonwoven fabric manufacturing process, currently, a latex bond method in which an adhesive is sprayed and bonded, a thermal bond method in which a polyolefin-based or polyester-based heat-adhesive fiber is used as a binder fiber, or both are bonded. Is used (see, for example, Patent Documents 1 to 3). However, in the bonding by the latex bond method, the adhesive permeates into the voids of the nonwoven fabric, resulting in problems such as a decrease in liquid retention and flexibility. Also, polyolefin-based and polyester-based thermal adhesiveness Bonding by a thermal bond method using fibers has problems such as a decrease in hydrophilicity, water retention and water absorption of the obtained nonwoven fabric due to the hydrophobicity derived from these materials.
Therefore, an airlaid nonwoven fabric produced by the above-mentioned production method as a nonwoven fabric for cosmetic products is not preferable because the chemical solution does not sufficiently penetrate into the nonwoven fabric and the flexibility is lowered, and the sheet is uncomfortable when touched to the skin.

特許公開2007−154163号公報Japanese Patent Publication No. 2007-154163 特許公開2001−329432号公報Japanese Patent Publication 2001-329432 特許公開2003−89958号公報Japanese Patent Publication No. 2003-89958

したがって、本発明の目的は、保液性、柔軟性を失わずにエアレイド不織布用熱接着繊維を提供することにある。   Accordingly, an object of the present invention is to provide a heat-bonding fiber for an airlaid nonwoven fabric without losing the liquid retaining property and flexibility.

本発明者らは上記の課題を解決するために鋭意検討した結果、分子内に水酸基を有するエチレンービニルアルコール系共重合体を用いた繊維をバインダー繊維として用いることで、親水性、保水性を維持したエアレイド不織布が得られることを見出した。   As a result of intensive studies to solve the above problems, the present inventors have used a fiber using an ethylene-vinyl alcohol copolymer having a hydroxyl group in the molecule as a binder fiber, thereby improving hydrophilicity and water retention. It has been found that a maintained airlaid nonwoven can be obtained.

すなわち、本発明はエチレン含有量5〜70モル%のエチレンービニルアルコール系共重合体からなる繊維であって、該繊維の繊維長が2〜30mm、かつ捲縮数が3〜30個/inchであることを特徴とするエアレイド不織布用繊維であり、好ましくはエチレンービニルアルコール共重合体(A)とエチレン−ビニルアルコール系共重合体以外の熱可塑性樹脂(B)とで構成される複合繊維であり、エチレンービニルアルコール共重合体(A)が繊維表面に存在していることを特徴とする上記のエアレイド不織布用繊維であり、さらに好ましくは該繊維を少なくとも10重量%以上含有してなるエアレイド不織布に関するものである。   That is, the present invention is a fiber comprising an ethylene-vinyl alcohol copolymer having an ethylene content of 5 to 70 mol%, wherein the fiber has a fiber length of 2 to 30 mm and a number of crimps of 3 to 30 / inch. It is a fiber for air laid nonwoven fabric characterized by being, The composite fiber comprised with thermoplastic resins (B) preferably other than ethylene-vinyl alcohol copolymer (A) and ethylene-vinyl alcohol type copolymer Wherein the ethylene-vinyl alcohol copolymer (A) is present on the fiber surface, and is a fiber for an airlaid nonwoven fabric, and more preferably contains at least 10% by weight of the fiber. The present invention relates to an airlaid nonwoven fabric.

本発明によれば、接着剤や、疎水性熱可塑性樹脂であるポリオレフィン系樹脂や、ポリエステル系樹脂をバインダー繊維に用いることなく、エアレイド用熱接着性繊維を提供することができるため、この繊維を用いることで得られたエアレイド不織布は、親水性、保水性、柔軟性を有するエアレイド不織布を得ることができる。   According to the present invention, it is possible to provide a heat-adhesive fiber for airlaid without using an adhesive, a polyolefin-based resin that is a hydrophobic thermoplastic resin, or a polyester-based resin as a binder fiber. The air-laid nonwoven fabric obtained by using can obtain an air-laid nonwoven fabric having hydrophilicity, water retention and flexibility.

以下、本発明について詳細に説明する。
本発明の繊維は、エチレンービニルアルコール系共重合体を原料として用いた溶融紡糸法により得ることができ、必要に応じて延伸処理、熱処理等を施しても良い。また、複合繊維を得る場合は、溶融紡糸法にて口金を変更することで得ることができる。たとえば、エチレン−ビニルアルコール共重合体(A)と、熱可塑性重合体(B)の複合繊維を得る場合、各々の原料を別々の押出機で溶融して、それらの溶融体を複合紡糸パックを有する紡糸装置に導入し、紡糸パック内で合流複合させて紡糸することにより得られる。
Hereinafter, the present invention will be described in detail.
The fiber of the present invention can be obtained by a melt spinning method using an ethylene-vinyl alcohol copolymer as a raw material, and may be subjected to stretching treatment, heat treatment, and the like as necessary. Moreover, when obtaining a composite fiber, it can obtain by changing a nozzle | cap | die with a melt spinning method. For example, when obtaining a composite fiber of an ethylene-vinyl alcohol copolymer (A) and a thermoplastic polymer (B), each raw material is melted in a separate extruder, and these melts are combined into a composite spin pack. It is obtained by introducing it into a spinning device having the same, and combining and spinning in a spinning pack.

本発明におけるエチレンービニルアルコール共重合体系繊維とは、エチレンと酢酸ビニルの共重合体のケン化物を成分とする繊維であり、該共重合体に含有されるエチレンの量は5〜70モル%のものが用いられる。エチレンの含有量が5モル%未満の場合、溶融紡糸性が悪化するため好ましくない。一方、エチレンの含有量が70モル%を超えた場合、本発明が目的とする親水性、保水性などの物性が低下するため好ましくない。好ましくは20〜50モル%である。   The ethylene-vinyl alcohol copolymer fiber in the present invention is a fiber containing a saponification product of a copolymer of ethylene and vinyl acetate as a component, and the amount of ethylene contained in the copolymer is 5 to 70 mol%. Is used. When the ethylene content is less than 5 mol%, melt spinnability deteriorates, which is not preferable. On the other hand, when the ethylene content exceeds 70 mol%, the physical properties such as hydrophilicity and water retention aimed at by the present invention are not preferred. Preferably it is 20-50 mol%.

本発明の繊維の繊度は目的に応じて選択すればよく、特に限定はされないが、0.5〜100dtex程度の範囲で用いられる。   The fineness of the fiber of the present invention may be selected according to the purpose and is not particularly limited, but is used in the range of about 0.5 to 100 dtex.

本発明の繊維の繊維長は2〜30mmの範囲であることが必要であり、3〜10mmの範囲であることが好ましい。繊維長が2mm未満の場合、エアレイド不織布として十分な強力を得ることができず、工程通過性が悪化するため好ましくない。また、繊維長が30mmを超えた場合、繊維同士が絡まり合い、空気開繊性が悪くなり不織布の目付け斑が引き起こされるなどの問題が生じるため好ましくない。   The fiber length of the fiber of the present invention needs to be in the range of 2 to 30 mm, and preferably in the range of 3 to 10 mm. When the fiber length is less than 2 mm, sufficient strength cannot be obtained as an air laid nonwoven fabric, and the process passability deteriorates, which is not preferable. Moreover, when the fiber length exceeds 30 mm, the fibers are entangled with each other, and problems such as poor air opening and causing unevenness of the nonwoven fabric occur, which is not preferable.

本発明の繊維は空気開繊性の観点から捲縮が付与されていることが好ましい。捲縮が付与されていることで、空気による衝撃または回転ドラム内壁面への衝突時に捲縮による弾性効果で未開繊状態の繊維塊が開繊しやすくなる。そのため、捲縮数は3〜30個/inchの範囲であることが必要であり、5〜20個/inchの範囲であることがより好ましい。捲縮数が3個/inch未満の場合、未開繊状態の繊維が発生しやすくなり風合が悪化するため好ましくない。また、捲縮数が30個/inchを超えた場合、空気開繊性が悪くなり、結束状となった欠点が発生しやすくなるため好ましくない。   The fibers of the present invention are preferably crimped from the viewpoint of air opening. By being crimped, a fiber lump in an unopened state can be easily opened by an elastic effect due to crimping upon impact by air or collision with the inner wall surface of the rotating drum. For this reason, the number of crimps needs to be in the range of 3 to 30 pieces / inch, and more preferably in the range of 5 to 20 pieces / inch. When the number of crimps is less than 3 / inch, unopened fibers are likely to be generated and the texture is deteriorated. On the other hand, when the number of crimps exceeds 30 / inch, the air-opening property is deteriorated, and a defect in a bundled shape tends to occur, which is not preferable.

本発明の繊維の140℃における乾熱収縮率は−20〜20%の範囲であることが好ましく、−15%〜15%の範囲であることがより好ましい。140℃における乾熱収縮率がマイナスであることは、つまり熱処理による伸張を示しており、この値が−20%未満であると熱処理時に本発明の繊維が伸張するため、不織布の寸法安定性が悪くなるため好ましくない。また、20%を超えた場合、スポット的な収縮が発生するため、不織布の寸法安定性が悪くなるだけでなく、目付け斑が発生するため好ましくない。なお、本発明でいう140℃における乾熱収縮率は後述する方法で測定される。   The dry heat shrinkage rate of the fiber of the present invention at 140 ° C. is preferably in the range of −20 to 20%, and more preferably in the range of −15% to 15%. That the dry heat shrinkage rate at 140 ° C. is negative, that is, indicates elongation due to heat treatment, and if this value is less than −20%, the fiber of the present invention stretches during heat treatment, so the dimensional stability of the nonwoven fabric is reduced. Since it gets worse, it is not preferable. On the other hand, if it exceeds 20%, spot-like shrinkage occurs, which is not preferable because not only the dimensional stability of the nonwoven fabric is deteriorated but also unevenness in appearance occurs. In the present invention, the dry heat shrinkage at 140 ° C. is measured by the method described later.

本発明の繊維の融点はエチレン含有量に応じて変化するため、その範囲は120℃〜230℃付近となるが、エチレン含有量が約40モル%以下の場合において、融点は170℃以上となるため、バインダー性能を発現させるためには高温での処理が必要になるため、不織布が収縮変形しやすくなり、目付斑などが発生する問題を有するが、その場合は、ウェブを湿潤状態にしてから熱処理を行い結合させる方法を実施することが好ましい。   Since the melting point of the fiber of the present invention changes depending on the ethylene content, the range is around 120 ° C. to 230 ° C., but when the ethylene content is about 40 mol% or less, the melting point is 170 ° C. or more. Therefore, in order to develop the binder performance, it is necessary to process at a high temperature, so that the nonwoven fabric tends to shrink and deform, and there is a problem that uneven spots etc. occur. It is preferable to carry out a heat treatment and bonding method.

本発明の繊維は単独であっても、他の熱可塑性重合体との複合繊維であってもよい。他の熱可塑性重合体としてポリオレフィン系樹脂、ポリエステル系樹脂、ポリアミド系樹脂、ポリ塩化ビニル、ポリ塩化ビニリデン、スチレン系樹脂、ポリ酢酸ビニル系樹脂、アクリル系樹脂、ポリ乳酸系樹脂、ポリカーボネート系樹脂、熱可塑性エラストマーなどの熱可塑性重合体が用いられ、エチレン共重合度の異なるエチレンービニルアルコール共重合体を用いても良い。   The fiber of the present invention may be a single fiber or a composite fiber with another thermoplastic polymer. Other thermoplastic polymers include polyolefin resins, polyester resins, polyamide resins, polyvinyl chloride, polyvinylidene chloride, styrene resins, polyvinyl acetate resins, acrylic resins, polylactic acid resins, polycarbonate resins, A thermoplastic polymer such as a thermoplastic elastomer is used, and ethylene-vinyl alcohol copolymers having different degrees of ethylene copolymerization may be used.

本発明の繊維を他の熱可塑性重合体との複合繊維とした場合、エチレンービニルアルコール共重合体(A)と熱可塑性重合体(B)の割合(質量比)は、構造(例えば、芯鞘型構造)に応じて選択でき、エチレンービニルアルコール共重合体(A)を少なくとも繊維表面の一部に有していれば特に限定されないが、エチレンービニルアルコール共重合体(A)の割合は10%以上であることが好ましい。エチレンービニルアルコール共重合体の割合が10%未満であると、熱接着性が低下するため好ましくない。   When the fiber of the present invention is a composite fiber with another thermoplastic polymer, the ratio (mass ratio) of the ethylene-vinyl alcohol copolymer (A) and the thermoplastic polymer (B) is the structure (for example, core It can be selected according to the sheath-type structure, and is not particularly limited as long as it has an ethylene-vinyl alcohol copolymer (A) on at least a part of the fiber surface, but the ratio of the ethylene-vinyl alcohol copolymer (A) Is preferably 10% or more. If the ratio of the ethylene-vinyl alcohol copolymer is less than 10%, the thermal adhesiveness is lowered, which is not preferable.

本発明の複合繊維の横断面構造としては、例えば、芯鞘型、海島型、サイドバイサイド型又は多層貼合型、放射状貼合型、ランダム複合型などが挙げられる。これらの横断面構造のうち、接着性の点から、エチレンービニルアルコール共重合体を少なくとも繊維表面の一部に有していればよいが、全表面を長さ方向に連続して占める構造である芯鞘型構造(すなわち、鞘部が湿熱接着性樹脂で構成された芯鞘型構造)が好ましい。   Examples of the cross-sectional structure of the conjugate fiber of the present invention include a core-sheath type, a sea-island type, a side-by-side type or a multilayer bonding type, a radial bonding type, and a random composite type. Of these cross-sectional structures, from the viewpoint of adhesiveness, it is sufficient that the ethylene-vinyl alcohol copolymer is at least part of the fiber surface, but the entire surface continuously occupies the length direction. A certain core-sheath type structure (that is, a core-sheath type structure in which the sheath part is composed of wet heat adhesive resin) is preferable.

本発明の繊維の断面形状はどのようなものであってもよく、円形または異形の形状とすることができる。異形断面の場合は、例えば偏平形、楕円形、三角形〜八角形等の角形、T字形、H字状、V字状、ドッグボーン(I字状)、3〜8葉形等の多葉形等の任意の形状とすることができ、それらの中空断面状などであってもよい。   The cross-sectional shape of the fiber of the present invention may be any shape, and may be a circular or irregular shape. In the case of an irregular cross-section, for example, flat, elliptical, triangular to octagonal, etc., T-shape, H-shape, V-shape, dogbone (I-shape), multi-leaf shape such as 3-8 leaf shape Any shape such as a hollow cross-section thereof may be used.

本発明の繊維は、さらに、慣用の添加剤、例えば、抗菌剤、消臭剤、難燃剤、熱安定剤、紫外線吸収剤、光安定剤、酸化防止剤、着色剤、帯電防止剤、可塑剤、潤滑剤、結晶化速度遅延剤などを含有していてもよく、これらの添加剤は、単独で又は二種以上組み合わせて使用できる。また、これらの添加剤は、繊維中に含まれていてもよく、繊維表面に担持されていてもよい。   The fibers of the present invention further comprise conventional additives such as antibacterial agents, deodorants, flame retardants, heat stabilizers, UV absorbers, light stabilizers, antioxidants, colorants, antistatic agents, and plasticizers. , Lubricants, crystallization rate retarders, and the like, and these additives may be used alone or in combination of two or more. Moreover, these additives may be contained in the fiber and may be carried on the fiber surface.

本発明の繊維に付与する油剤成分は、空気開繊性を良好にすることと、静電気の発生を抑制する油剤であれば特に限定されないが、アルキル燐酸アルカリ金属塩、アルキルエーテル型ノニオン、4級アンモニウム型カチオン活性剤、両性活性剤、変性シリコーンなどの成分を目的に応じて含まれた組成が好ましい例として挙げられる。   The oil component to be imparted to the fiber of the present invention is not particularly limited as long as it is an oil agent that improves the air opening property and suppresses the generation of static electricity. Alkyl phosphate alkali metal salt, alkyl ether type nonion, quaternary A preferred example includes a composition containing components such as an ammonium type cationic activator, an amphoteric activator, and a modified silicone depending on the purpose.

本発明の繊維を用いて得られたエアレイド不織布の保水率は2000%以上であることが望ましい。保水率が2000%未満の場合、例えば水溶性の薬液などを十分に保持することができず、コスメ用として用いることができないため好ましくない。   The water retention rate of the airlaid nonwoven fabric obtained using the fiber of the present invention is desirably 2000% or more. When the water retention rate is less than 2000%, for example, it is not preferable because a water-soluble chemical solution cannot be sufficiently retained and cannot be used for cosmetics.

本発明の繊維を用いて得られたエアレイド不織布の保油率は2000%以上であることが望ましい。保油率が2000%未満の場合、例えばエッセンシャルオイルなどの薬液などを十分に保持することができず、コスメ用として用いることができないため好ましくない。   The oil retention of the air-laid nonwoven fabric obtained using the fiber of the present invention is desirably 2000% or more. When the oil retention is less than 2000%, for example, a chemical solution such as essential oil cannot be sufficiently retained and cannot be used for cosmetics.

本発明の繊維を用いて得られたエアレイド不織布の脱水率は1000%以上であることが望ましい。脱水率が1000%未満の場合、例えば水溶性の薬液などを含ませた不織布を肌に接触させた際、いつまでも肌にまとわりつく感触残るため、例えばフェイスマスクなどの用途として用いた場合、使用時の感触が良くないため好ましくない。   The air-laid nonwoven fabric obtained using the fiber of the present invention preferably has a dehydration rate of 1000% or more. When the dehydration rate is less than 1000%, for example, when a non-woven fabric containing a water-soluble chemical solution is brought into contact with the skin, it will remain touching the skin forever. For example, when used as a face mask, It is not preferable because the touch is not good.

本発明の繊維を用いて得られたエアレイド不織布の剛軟性は90mm以下であることが望ましい。剛軟性が90mmを超えた場合、不織布が硬い感触となり、例えばフェイスマスクなどの用途として用いた場合、顔の形状に沿って不織布が変形することが出来なくなるため、不織布に接触しない空間が発生し肌への薬液が十分に浸透しないなどの問題が発生するため好ましくない。   Desirably, the air-laid nonwoven fabric obtained by using the fiber of the present invention has a bending resistance of 90 mm or less. When the bending resistance exceeds 90 mm, the nonwoven fabric has a hard feel. For example, when used as a face mask, the nonwoven fabric cannot be deformed along the shape of the face. This is not preferable because problems such as insufficient penetration of the chemical into the skin occur.

以下、実施例により本発明を具体的に説明するが、本発明は何等これらに限定されるものではない。   EXAMPLES Hereinafter, although an Example demonstrates this invention concretely, this invention is not limited to these at all.

<繊維繊度 dtex>
JIS L1015「化学繊維ステープル試験方法(8.5.1)」に準じて評価した。
<繊維長 mm>
JIS L1015「化学繊維ステープル試験方法(8.4.1)」に準じて評価した。
<繊維の捲縮数 個/inch>
JIS L1015「化学繊維ステープル試験方法(8.12.1)」に準じて評価した。
<Fiber fineness dtex>
Evaluation was made according to JIS L1015 “Testing method for chemical fiber staples (8.5.1)”.
<Fiber length mm>
Evaluation was made according to JIS L1015 “Testing method for chemical fiber staples (8.4.1)”.
<Number of crimped fibers / inch>
The evaluation was made according to JIS L1015 “Testing method for chemical fiber staples (8.12.1)”.

<繊維の乾熱収縮率 %>
繊維を約50cmにカットし、適切な性能をもつ垂下装置を用いて、結び目間隔が35cmとなるように両端を結ぶ。直示天秤を用いて重量を測定し、1デニール当たり50mgの初荷重を付加して、結び目間の糸長を測定する(L1)。次に、初荷重をはずし、熱風乾燥機にて140℃、15分間熱処理を行う。放冷後、再び1デニール当たり50mgの荷重を付加して、結び目間の糸長を測定する(L2)。
以下の式より乾熱収縮率を算出した。
乾熱収縮率(%)=[(L1−L2)/L1]×100
<Dry heat shrinkage% of fiber>
Cut the fiber to about 50 cm and use a drooping device with appropriate performance to tie both ends so that the knot spacing is 35 cm. The weight is measured using a direct balance, an initial load of 50 mg per denier is added, and the yarn length between the knots is measured (L1). Next, the initial load is removed, and heat treatment is performed at 140 ° C. for 15 minutes in a hot air dryer. After allowing to cool, a load of 50 mg per denier is added again and the yarn length between the knots is measured (L2).
The dry heat shrinkage was calculated from the following formula.
Dry heat shrinkage (%) = [(L1-L2) / L1] × 100

<不織布の保水率、保油率 %>
JIS L1913「一般短繊維不織布試験法(6.9.2)」に準じて評価。なお試験液として、保水率の場合はイオン交換水、保油率の場合はサラダ油を用いた。
<Nonwoven fabric water retention, oil retention%>
Evaluated according to JIS L1913 “General Short Fiber Nonwoven Fabric Test Method (6.9.2)”. As the test solution, ion-exchanged water was used for the water retention rate, and salad oil was used for the oil retention rate.

<不織布の脱水率 %>
5cm×5cmの試験片を用い、20分間イオン交換水に浸漬させた後の重量(a)を測定し、その後、遠心脱水機を用い1000Gにて2分間脱水処理を行った後の重量(b)を測定し、下記式より脱水率を算出した。
脱水率(%)=(a−b)/b×100 (a:浸漬処理後の重量、b:脱水後の重量)
<Dehydration rate of nonwoven fabric%>
Using a test piece of 5 cm × 5 cm, the weight (a) after being immersed in ion-exchanged water for 20 minutes was measured, and then the weight after being subjected to dehydration treatment at 1000 G for 2 minutes using a centrifugal dehydrator (b ) And the dehydration rate was calculated from the following formula.
Dehydration rate (%) = (ab) / b × 100 (a: weight after immersion treatment, b: weight after dehydration)

<不織布の剛軟性 mm>
JIS L1913「一般短繊維不織布試験法(6.9.3) カンチレバー法」に準じて評価した。
<Flexibility of nonwoven fabric mm>
The evaluation was made according to JIS L1913 “General Short Fiber Nonwoven Fabric Test Method (6.9.3) Cantilever Method”.

[実施例1〜8]
(1)表1に示すエチレン含有量のエチレンービニルアルコール共重合体(A)を鞘成分とし、ポリエチレンテレフタレート(株式会社クラレ製、極限粘度[η]=0.59)から成る熱可塑性重合体(B)を芯成分として、複合紡糸装置を用いて、丸断面口金にて、複合比率(A/B)=50/50(重量比)で芯鞘型に接合して紡出した。紡出した糸条を冷却固化した後、引取ローラーを介してボビンに捲き取った。
(2)次いで、この捲取糸を延伸倍率2倍で熱延伸し、油剤浴にて油剤を付与後、機械捲縮付与処理を施した。機械捲縮付与処理は、通常のスタッファ型捲縮付与装置等の捲縮付与装置を用いて行なった。捲縮付与処理に引き続き、繊維を熱風乾燥した後、カットすることでエチレンービニルアルコール系共重合体からなる短繊維を得た。各繊維物性を表1に示す。
[Examples 1 to 8]
(1) A thermoplastic polymer made of polyethylene terephthalate (manufactured by Kuraray Co., Ltd., intrinsic viscosity [η] = 0.59) having an ethylene-vinyl alcohol copolymer (A) having an ethylene content shown in Table 1 as a sheath component. Using (B) as a core component, a composite spinning device was used to join a core-sheath mold with a round cross-section die at a composite ratio (A / B) = 50/50 (weight ratio). The spun yarn was cooled and solidified, and then wound on a bobbin via a take-up roller.
(2) Next, this crimped yarn was hot-drawn at a draw ratio of 2 times, and after applying the oil in an oil bath, a mechanical crimping treatment was performed. The mechanical crimping treatment was performed using a crimping device such as a normal stuffer type crimping device. Subsequent to the crimping treatment, the fiber was dried with hot air and then cut to obtain a short fiber made of an ethylene-vinyl alcohol copolymer. Each fiber property is shown in Table 1.

上記の製造方法にて得られた短繊維を用いて、実施例1〜7では上記短繊維を100重量%、実施例8では上記短繊維10重量%、パルプ(ウェアーハウザー社製、木材粉砕パルプ)90重量%を混合したものを用い、Dan-Web forming社のフォーミングドラムユニットを用いて目付け50g/mのエアレイド不織布を製造した。各不織布の物性を表1に示す。 Using short fibers obtained by the above production method, the short fibers were 100% by weight in Examples 1 to 7, 10% by weight of short fibers in Example 8, pulp (Wood Hauser, wood-pulverized pulp) ) An air laid nonwoven fabric having a basis weight of 50 g / m 2 was manufactured using a blending drum unit manufactured by Dan-Web forming using 90% by weight. Table 1 shows the physical properties of each nonwoven fabric.

[比較例1]
繊維長が1mmであること以外は実施例1と同一である短繊維を用いてエアレイド不織布を製造したが、繊維長が短すぎるため、不織布内での繊維間接着が十分になされず、熱処理後のワイヤーから捲取りロールへの導紙工程にてウェブ切れが発生するため、エアレイド不織布を採取することができなかった。
[Comparative Example 1]
The air laid nonwoven fabric was manufactured using the same short fiber as in Example 1 except that the fiber length was 1 mm. However, since the fiber length was too short, the inter-fiber adhesion in the nonwoven fabric was not sufficient, and after heat treatment Since the web breakage occurred in the paper guiding process from the wire to the scissor roll, the air-laid nonwoven fabric could not be collected.

[比較例2]
繊維長が35mmであること以外は実施例1と同一である短繊維を用いてエアレイド不織布を製造したが、繊維長が長すぎるため、フォーミングヘッド内での開繊が十分になされず、スリット部から繊維が放出されないため、エアレイド不織布を採取することができなかった。
[Comparative Example 2]
An air laid nonwoven fabric was produced using the same short fiber as in Example 1 except that the fiber length was 35 mm. However, since the fiber length was too long, the opening in the forming head was not sufficiently performed, and the slit portion Since no fiber was released from the airlaid fabric, the airlaid nonwoven fabric could not be collected.

[比較例3]
捲縮数が2個/inchであること以外は実施例1と同一である短繊維を用いてエアレイド不織布を製造したが、捲縮数が少なすぎるため繊維間絡合が十分になされず、不織布自体の強力が低下し、熱処理後のワイヤーから捲取りロールへの導紙工程にてウェブ切れが発生するため、エアレイド不織布を採取することができなかった。
[Comparative Example 3]
An airlaid nonwoven fabric was produced using the same short fibers as in Example 1 except that the number of crimps was 2 / inch. However, since the number of crimps was too small, the interfiber entanglement was not sufficient, and the nonwoven fabric. Since the strength of itself decreased and web breakage occurred in the paper introduction process from the wire after heat treatment to the scooping roll, the air-laid nonwoven fabric could not be collected.

[比較例4]
捲縮数35個/inchであること以外は実施例1と同一である短繊維を用いてエアレイド不織布を製造したが、捲縮数が多すぎるためフォーミングヘッド内での開繊が十分になされず、スリット部から繊維が放出されないため、エアレイド不織布を採取することができなかった。
[Comparative Example 4]
An airlaid nonwoven fabric was produced using the same short fibers as in Example 1 except that the number of crimps was 35 / inch. However, since the number of crimps was too large, the opening in the forming head was not sufficiently performed. Since no fiber was released from the slit portion, the air-laid nonwoven fabric could not be collected.

[比較例5]
エチレン含有量が4モル%のエチレンービニルアルコール系共重合体を用いること以外は実施例1と同じ条件にて溶融紡糸したが、紡糸性が悪く、目的とする短繊維を採取するにいたらなかった。
[Comparative Example 5]
Except for using an ethylene-vinyl alcohol copolymer having an ethylene content of 4 mol%, melt spinning was performed under the same conditions as in Example 1, but the spinnability was poor, and it was not necessary to collect the desired short fibers. It was.

[比較例6]
エチレン含有量が75モル%のエチレンービニルアルコール系共重合体を用いること以外は実施例1と同じ繊度、繊維長、捲縮数からなる短繊維を製造したが、該短繊維を用いたエアレイド不織布は、不織布の親水性が低下するため、保水率が劣ったものとなった。
[Comparative Example 6]
A short fiber having the same fineness, fiber length, and number of crimps as in Example 1 was produced except that an ethylene-vinyl alcohol copolymer having an ethylene content of 75 mol% was used. Airlaid using the short fiber The nonwoven fabric was inferior in water retention because the hydrophilicity of the nonwoven fabric decreased.

[比較例7]
実施例1と同一のエチレンービニルアルコール系共重合体からなる繊維の重量比率が8重量%、パルプの重量比率が92重量%からなるエアレイド不織布を製造したが、バインダー繊維として機能するエチレンービニルアルコール系共重合体からなる繊維の重量比率が少ないため、不織布自体の強力が低下し、熱処理後のワイヤーから捲取りロールへの導紙工程にてウェブ切れが発生するため、エアレイド不織布を採取することができなかった。
[Comparative Example 7]
An airlaid nonwoven fabric was produced in which the weight ratio of the fiber made of the same ethylene-vinyl alcohol copolymer as in Example 1 was 8% by weight and the weight ratio of the pulp was 92% by weight, but ethylene-vinyl functioning as a binder fiber. Since the weight ratio of the fiber made of alcoholic copolymer is small, the strength of the nonwoven fabric itself is reduced, and the web breakage occurs in the paper introduction process from the wire after heat treatment to the take-up roll. I couldn't.

[比較例8]
バインダー繊維として、ポリエチレン(PE)を鞘成分とし、ポリエチレンテレフタレート(PET)からなる熱可塑性重合体を芯成分とした繊維(帝人ファイバー社製、1.7dtex,3mm)を用いたエアレイド不織布を製造したが、不織布の親水性が低下するため、保水率が劣ったものとなった。また剛軟性も高く、風合いの硬い不織布であった。
[Comparative Example 8]
An airlaid nonwoven fabric was produced using fibers (1.7 ttex, 3 mm, manufactured by Teijin Fibers Ltd.) having polyethylene (PE) as a sheath component and a thermoplastic polymer made of polyethylene terephthalate (PET) as a core component as binder fibers. However, since the hydrophilic property of the nonwoven fabric was lowered, the water retention rate was inferior. Further, the nonwoven fabric had high bending resistance and a hard texture.

[比較例9]
バインダー繊維として、非晶性ポリエチレンテレフタレート(株式会社クラレ製、イソフタル酸40モル%共重合PET、極限粘度[η]=0.59)を鞘成分とし、ポリエチレンテレフタレート(PET)から成る熱可塑性重合体を芯成分とし、芯鞘比=50/50の繊維を用いてエアレイド不織布を製造したが、不織布の親水性が低下するため、保水率が劣ったものとなった。また剛軟性も高く、風合いの硬い不織布であった。
[Comparative Example 9]
Thermoplastic polymer made of polyethylene terephthalate (PET) with non-crystalline polyethylene terephthalate (manufactured by Kuraray Co., Ltd., isophthalic acid 40 mol% copolymerized PET, intrinsic viscosity [η] = 0.59) as a sheath component as binder fiber The air-laid nonwoven fabric was manufactured using a fiber having a core-sheath ratio of 50/50, but the water retention was poor because the hydrophilicity of the nonwoven fabric was lowered. Further, the nonwoven fabric had high bending resistance and a hard texture.

Figure 2013170340
Figure 2013170340

Figure 2013170340
Figure 2013170340

本発明により得られたエアレイド不織布用繊維は、接着剤や、疎水性熱可塑性樹脂であるポリオレフィン系樹脂や、PET系樹脂をバインダー繊維に用いることなく、エアレイド用熱接着性繊維を提供することができるため、該繊維を用いることで得られたエアレイド不織布は、シート強力を有しながら、親水性、保水性、通気性、嵩高性、柔軟性を有するエアレイド不織布を得ることができる。このため、従来のエアレイド不織布では用途展開が困難であったコスメ分野への応用が十分可能となる。   The fiber for airlaid nonwoven fabric obtained by the present invention can provide a heat adhesive fiber for airlaid without using an adhesive, a polyolefin resin that is a hydrophobic thermoplastic resin, or a PET resin as a binder fiber. Therefore, the air-laid nonwoven fabric obtained by using the fiber can provide an air-laid nonwoven fabric having hydrophilicity, water retention, air permeability, bulkiness and flexibility while having sheet strength. For this reason, the application to the cosmetics field | area which was difficult for the use expansion | deployment with the conventional airlaid nonwoven fabric becomes possible sufficiently.

Claims (3)

エチレン含有量5〜70モル%のエチレンービニルアルコール系共重合体からなる繊維であって、該繊維の繊維長が2〜30mm、かつ捲縮数が3〜30個/inchであることを特徴とするエアレイド不織布用繊維。   A fiber comprising an ethylene-vinyl alcohol copolymer having an ethylene content of 5 to 70 mol%, wherein the fiber has a fiber length of 2 to 30 mm and a number of crimps of 3 to 30 / inch. An airlaid nonwoven fabric. エチレンービニルアルコール共重合体(A)とエチレンービニルアルコール系共重合体以外の熱可塑性樹脂(B)とで構成される複合繊維であり、エチレンービニルアルコール共重合体(A)が繊維表面に存在していることを特徴とする請求項1記載のエアレイド不織布用繊維。   A composite fiber composed of an ethylene-vinyl alcohol copolymer (A) and a thermoplastic resin (B) other than an ethylene-vinyl alcohol copolymer, and the ethylene-vinyl alcohol copolymer (A) is a fiber surface. The air-laid nonwoven fabric according to claim 1, wherein the fiber is present in the air-laid nonwoven fabric. 請求項1または2に記載の繊維を少なくとも10重量%以上用いたエアレイド不織布。   An airlaid nonwoven fabric using at least 10% by weight or more of the fiber according to claim 1 or 2.
JP2012036883A 2012-02-23 2012-02-23 Fiber for air-laid nonwoven fabric and air-laid nonwoven fabric using the fiber Pending JP2013170340A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015059288A (en) * 2013-09-20 2015-03-30 株式会社クラレ Nonwoven fiber structure body
WO2018214148A1 (en) * 2017-05-26 2018-11-29 Estee Lauder International, Inc. Cosmetic substrate comprising crimped fibers

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JP2002203530A (en) * 2000-12-27 2002-07-19 Daiwabo Co Ltd Battery separator and alkaline storage battery using the same
JP2007070798A (en) * 2006-11-02 2007-03-22 Teijin Fibers Ltd Polyester-based staple fiber and nonwoven fabric comprising the same
JP2007312931A (en) * 2006-05-24 2007-12-06 Daiwabo Co Ltd Wiper
JP2009280920A (en) * 2008-05-19 2009-12-03 Es Fibervisions Co Ltd Conjugated fiber for producing air-laid nonwoven fabric and method for producing high-density air-laid nonwoven fabric

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002203530A (en) * 2000-12-27 2002-07-19 Daiwabo Co Ltd Battery separator and alkaline storage battery using the same
JP2007312931A (en) * 2006-05-24 2007-12-06 Daiwabo Co Ltd Wiper
JP2007070798A (en) * 2006-11-02 2007-03-22 Teijin Fibers Ltd Polyester-based staple fiber and nonwoven fabric comprising the same
JP2009280920A (en) * 2008-05-19 2009-12-03 Es Fibervisions Co Ltd Conjugated fiber for producing air-laid nonwoven fabric and method for producing high-density air-laid nonwoven fabric

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015059288A (en) * 2013-09-20 2015-03-30 株式会社クラレ Nonwoven fiber structure body
WO2018214148A1 (en) * 2017-05-26 2018-11-29 Estee Lauder International, Inc. Cosmetic substrate comprising crimped fibers

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