JP2006299425A - Water-absorbing nonwoven fabric laminate - Google Patents
Water-absorbing nonwoven fabric laminate Download PDFInfo
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- JP2006299425A JP2006299425A JP2005117854A JP2005117854A JP2006299425A JP 2006299425 A JP2006299425 A JP 2006299425A JP 2005117854 A JP2005117854 A JP 2005117854A JP 2005117854 A JP2005117854 A JP 2005117854A JP 2006299425 A JP2006299425 A JP 2006299425A
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- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
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- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
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- 229920000742 Cotton Polymers 0.000 description 1
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- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Laminated Bodies (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
本発明は、熱可塑性合成繊維不織布において、高い強度を損なうことなく、高い吸水性と保水性を有する吸水性不織布積層体に関するものである。 TECHNICAL FIELD The present invention relates to a water-absorbent nonwoven fabric laminate having high water absorption and water retention without impairing high strength in a thermoplastic synthetic fiber nonwoven fabric.
従来から、衛生材料や一般生活関連材料あるいは農業資材用、産業資材用の素材として、ポリアミドやポリエステル、ポリプロピレン等の汎用の熱可塑性合成繊維からなる不織布が知られているが、これらの不織布は、一般に疎水性であり、吸水性、保水性に乏しいものである。これまでにも、これら合繊からなる不織布に吸水性を付与するために、各種の提案がなされている。 Conventionally, non-woven fabrics made of general-purpose thermoplastic synthetic fibers such as polyamide, polyester, and polypropylene are known as sanitary materials, general life-related materials or agricultural materials, and industrial materials. Generally, it is hydrophobic and has poor water absorption and water retention. Various proposals have been made so far to impart water absorbency to nonwoven fabrics made of these synthetic fibers.
具体的には、合成繊維を親水性物質で表面被覆する方法(例えば、特許文献1)、アルキルフォスフェート金属塩を付着させる方法(例えば特許文献2)、繊維の表面あるいは断面形状を変化させる方法(例えば、特許文献3)、繊維に多孔性を付与する方法(例えば、特許文献4)、吸水ポリマーと吸水繊維を用いる方法(例えば、特許文献5)、ポリアルキレンオキシド変性物またはこの変生物とポリアミドまたはポリエステルとの混合物を鞘成分とする芯鞘型混合繊維を用いる方法(特許文献6)等を挙げることが出来る。 Specifically, a method of covering the surface of a synthetic fiber with a hydrophilic substance (for example, Patent Document 1), a method of attaching an alkyl phosphate metal salt (for example, Patent Document 2), a method of changing the surface or cross-sectional shape of the fiber (For example, Patent Document 3), a method for imparting porosity to a fiber (for example, Patent Document 4), a method using a water-absorbing polymer and a water-absorbing fiber (for example, Patent Document 5), a polyalkylene oxide modified product or this metamorphosis Examples thereof include a method using a core-sheath type mixed fiber having a mixture with polyamide or polyester as a sheath component (Patent Document 6).
しかしながら、合繊繊維を親水性物質で表面被覆する方法やアルキルフォスフェート金属塩を付着させる方法は、初期の親水性には優れるものの、吸水性および保水性という点では十分な性能を示さない。
吸水ポリマーと吸水繊維を用いる方法では吸水性に優れるものの、吸水ポリマーとの不織布積層体である為、一般に高強度のものを得ることは困難である。
繊維の表面あるいは断面形状を変化させる方法や多孔性を付与する方法は、後加工や特殊な製法を必要としコスト面で不利である等の問題がある。
However, the method of covering the synthetic fiber with a hydrophilic substance and the method of attaching an alkyl phosphate metal salt are excellent in initial hydrophilicity but do not exhibit sufficient performance in terms of water absorption and water retention.
Although a method using a water-absorbing polymer and a water-absorbing fiber is excellent in water absorption, it is generally difficult to obtain a high-strength material because it is a nonwoven fabric laminate with a water-absorbing polymer.
The method of changing the surface or cross-sectional shape of the fiber and the method of imparting porosity have problems such as being disadvantageous in terms of cost because it requires post-processing and a special manufacturing method.
また、ポリアルキレンオキシド変性物を用いる方法は吸水性には優れるものの、寸法安定性が悪く、ポリアルキレンオキシド変性物は曳糸性に乏しく、芯鞘型の繊維構造や他の熱可塑性樹脂との混合繊維でなければ繊維化が困難である等の問題があった。
一方、吸水性を有する不織布として、木綿や麻等の天然繊維が交絡一体化してなる、いわゆるスパンレース不織布が知られているが、この不織布は強力が低く、また繊維自体が熱可塑性でないために、不織不化を図るの際して加工方法が限定されるものであった。
Although the method using a polyalkylene oxide-modified product is excellent in water absorption, the dimensional stability is poor, and the polyalkylene oxide-modified product is poor in spinnability, so that the core-sheath fiber structure and other thermoplastic resins can be used. There was a problem that it would be difficult to make fibers unless the fibers were mixed.
On the other hand, as a nonwoven fabric having water absorbency, a so-called spunlace nonwoven fabric is known in which natural fibers such as cotton and hemp are entangled and integrated, but this nonwoven fabric has low strength and the fibers themselves are not thermoplastic. However, the processing method is limited when the nonwoven fabric is made non-woven.
本発明は、疎水性合成繊維不織布に吸水性を付与する上で、吸水性を付与する為の後加工の必要がなくコスト面で有利であり、かつ製造が容易で、十分な吸水性、保水性を有し、高強度である不織布を提供することを目的とするものである。 The present invention is advantageous in terms of cost because it does not require post-processing for imparting water absorbency to impart hydrophobicity to a hydrophobic synthetic fiber nonwoven fabric, and is easy to manufacture and has sufficient water absorbency and water retention. It aims at providing the nonwoven fabric which has property and is high intensity | strength.
本発明者らは、上記の課題を解決すべく鋭意検討した結果、ポリアルキレングリコールを共重合した吸水性繊維から構成される吸水性不織布層と、熱可塑性繊維不織布層を積層させることで、飛躍的に吸水性が向上し、高強力である不織布積層体を得ることができた。
すなわち、本発明は、以下の通りである。
(1)ポリアルキレングリコールを共重合した熱可塑吸水性樹脂を用いて得られる吸水性繊維から構成される吸水性不織布層と、熱可塑性繊維からなる不織布層から形成される積層体であり、該吸水性繊維が積層体の全重量に対して1〜99重量%含まれていることを特徴とする吸水性不織布積層体。
As a result of intensive studies to solve the above-mentioned problems, the present inventors made a leap forward by laminating a water-absorbing nonwoven fabric layer composed of water-absorbing fibers copolymerized with polyalkylene glycol and a thermoplastic fiber nonwoven fabric layer. In particular, it was possible to obtain a nonwoven fabric laminate having improved water absorption and high strength.
That is, the present invention is as follows.
(1) A laminate formed from a water-absorbing nonwoven fabric layer composed of a water-absorbing fiber obtained by using a thermoplastic water-absorbing resin copolymerized with a polyalkylene glycol, and a nonwoven fabric layer composed of a thermoplastic fiber, A water-absorbent nonwoven fabric laminate comprising 1 to 99% by weight of water-absorbent fibers based on the total weight of the laminate.
(2)JIS−L−1096滴下法による吸水速度が50秒以下であり、且つ保水率が7%以上であることを特徴とする上記(1)に記載の吸水性不織布積層体。
(3)前記熱可塑性吸水樹脂が、ポリテトラメチレンテレフタレートを主成分とするポリエステルとポリアルキレングリコールとの共重合体であり、ポリアルキレングリコールの共重合量が5〜90重量%である共重合ポリエステル系樹脂であることを特徴とする上記(1)又は(2)に記載の吸水性不織布積層体
(2) The water-absorbent nonwoven fabric laminate as described in (1) above, wherein the water absorption rate by a JIS-L-1096 dropping method is 50 seconds or less and the water retention is 7% or more.
(3) The thermoplastic water-absorbing resin is a copolymer of a polyester mainly composed of polytetramethylene terephthalate and a polyalkylene glycol, and the copolymerized polyester has a copolymerization amount of 5 to 90% by weight. A water-absorbent nonwoven fabric laminate as described in (1) or (2) above, wherein the laminate is a water-based resin
(4)前記吸水性不織布層の片面あるいは両面に、熱可塑性樹脂からなる不織布層が接合されてなる2層以上の多層構造を有することを特徴とする上記(1)〜(3)のいずれかに記載の吸水性不織布積層体。
(5)前記吸水性不織布層が吸水性連続長繊維からなることを特徴とする上記(1)〜(4)のいずれかに記載の吸水性不織布積層体。
(6)前記吸水性不織布層が、スパンボンド法あるいはメルトブローン法で形成されることを特徴とする上記(1)〜(5)のいずれかに記載の吸水性不織布積層体。
(4) Any one of the above (1) to (3), wherein the water-absorbing nonwoven fabric layer has a multilayer structure of two or more layers in which a nonwoven fabric layer made of a thermoplastic resin is bonded to one side or both sides. The water-absorbent nonwoven fabric laminate described in 1.
(5) The water-absorbing nonwoven fabric layered product according to any one of (1) to (4), wherein the water-absorbing nonwoven fabric layer is composed of water-absorbing continuous long fibers.
(6) The water-absorbing nonwoven fabric laminate according to any one of (1) to (5), wherein the water-absorbing nonwoven fabric layer is formed by a spunbond method or a melt blown method.
(7)前記熱可塑性繊維が、ポリオレフィン系またはポリアミド系またはポリエステル系であることを特徴とする上記(1)〜(6)に記載の吸水性不織布積層体。
(8)熱可塑性繊維からなる不織布層が、連続長繊維からなることを特徴とする上記(1)〜(7)記載の吸水性不織布積層体。
(9)熱可塑性繊維からなる不織布層が、スパンボンド法あるいはメルトブロー法で形成された不織布であることを特徴とする上記(1)〜(8)のいずれかに記載の吸水性不織布積層体。
(7) The water-absorbent nonwoven fabric laminate according to any one of (1) to (6) above, wherein the thermoplastic fiber is a polyolefin, polyamide, or polyester.
(8) The water-absorbent nonwoven fabric laminate as described in any one of (1) to (7) above, wherein the nonwoven fabric layer made of thermoplastic fibers is made of continuous long fibers.
(9) The water-absorbent nonwoven fabric laminate according to any one of the above (1) to (8), wherein the nonwoven fabric layer made of thermoplastic fibers is a nonwoven fabric formed by a spunbond method or a melt blow method.
(10)吸水性不織布積層体が、部分熱圧着法またはウォータージェット法またはニードルパンチ法で所定の形状を保持していることを特徴とする上記(1)〜(9)のいずれかに記載の吸水性不織布積層体。
(11)前記吸水性不織布が、熱可塑性樹脂からなるスパンボンド不織布を移動するウェブ捕集面上堆積させ、その上にメルトブローン法によって形成される吸水性繊維を直接堆積させ、さらにその上に熱可塑性樹脂からなるスパンボンド不織布を直接堆積させて熱エンボス処理により、積層体が圧着さてれなることを特徴とする上記(1)〜(10)に記載の吸水性不織布積層体。
(10) The water-absorbing nonwoven fabric laminate is maintained in a predetermined shape by a partial thermocompression bonding method, a water jet method, or a needle punch method, as described in any one of (1) to (9) above Water absorbent non-woven laminate.
(11) The water-absorbing nonwoven fabric is deposited on a moving web collecting surface of a spunbond nonwoven fabric made of a thermoplastic resin, and water-absorbing fibers formed by a melt blown method are directly deposited thereon, and heat is further deposited thereon. The water-absorbent nonwoven fabric laminate as described in any one of (1) to (10) above, wherein the laminate is pressure-bonded by directly depositing a spunbond nonwoven fabric made of a plastic resin and heat embossing.
本発明の熱可塑性吸水性繊維を用いた吸水性不織布積層体は、吸水性付与の為の後加工の必要がなく、コスト面で有利であり、吸水性繊維の比率によって積層体の強度と保水性を任意に制御でき、かつ、湿潤時の強度低下が小さく、取り扱い性に優れており、吸水吸放湿性を要求される用途に好適に利用できる。 The water-absorbent nonwoven fabric laminate using the thermoplastic water-absorbing fiber of the present invention does not require post-processing for imparting water absorption, and is advantageous in terms of cost. Therefore, it can be suitably used for applications that require water absorption / absorption and moisture absorption.
本発明の吸水性不織布積層体は、ポリアルキレングリコールを共重合した熱可塑吸水性
樹脂を用いて得られる吸水性繊維から構成される吸水性不織布層と、熱可塑性繊維からなる不織布層から形成される吸水性不織布積層体であり、該吸水性繊維が積層体の全重量に対して1〜99重量%含まれることを特徴とする吸水性不織布積層体である。また、吸水性不織布積層体であって、JIS−L−1096滴下法による吸水速度が50秒以下であり、且つ保水率が7%以上であることを特徴とする。
The water-absorbing nonwoven fabric laminate of the present invention is formed from a water-absorbing nonwoven fabric layer composed of water-absorbing fibers obtained by using a thermoplastic water-absorbing resin copolymerized with polyalkylene glycol, and a nonwoven fabric layer composed of thermoplastic fibers. A water-absorbing nonwoven fabric laminate, wherein the water-absorbing fibers are contained in an amount of 1 to 99% by weight based on the total weight of the laminate. Moreover, it is a water absorptive nonwoven fabric laminated body, Comprising: The water absorption rate by a JIS-L-1096 dripping method is 50 second or less, and a water retention is 7% or more, It is characterized by the above-mentioned.
以下に、各不織布の構成について述べる。
〔吸水性不織布層〕
本発明に用いる吸水性不織布層は、吸水性繊維から構成され、吸水性繊維は、吸水特性を有する吸水性樹脂から構成される。
この吸水性樹脂の吸水特性は、40℃、相対湿度80%下での吸湿率が7%以上、保水率が15%以上であり、好ましくは40℃、相対湿度80%下吸湿率が9%以上、保水率が20%以上の吸水特性を有する。
Below, the structure of each nonwoven fabric is described.
(Water-absorbing non-woven fabric layer)
The water-absorbing nonwoven fabric layer used in the present invention is composed of water-absorbing fibers, and the water-absorbing fibers are composed of a water-absorbing resin having water-absorbing properties.
The water-absorbing properties of this water-absorbing resin are as follows: moisture absorption at 40 ° C. and relative humidity of 80% is 7% or more, water retention is 15% or more, preferably 40 ° C. and relative humidity of 80% is 9%. As described above, the water retention rate is 20% or more.
吸水性繊維が吸水性不織布積層体(以後、「積層体」という。)の全重量に対して1〜99重量%の範囲であり、特に5〜80重量%含まれることが好ましい。吸水性繊維の含有量は、望みの吸水レベルに合わせて適宜設定でき、吸水特性と積層体強度のバランスを考慮して、設計できる。
吸水性樹脂は、ポリテトラメチレンテレフタレート主成分とするポリエステルとポリエチレングリコールとの共重合体からなる樹脂であり、ポリエチレングリコールの共重合量としては5〜90重量%、好ましくは10〜80重量%であり、特に好ましくは30〜60重量%の範囲である。
The water-absorbent fibers are in the range of 1 to 99% by weight, particularly preferably 5 to 80% by weight, based on the total weight of the water-absorbent nonwoven fabric laminate (hereinafter referred to as “laminate”). The water-absorbing fiber content can be set as appropriate according to the desired water absorption level, and can be designed in consideration of the balance between water absorption characteristics and laminate strength.
The water-absorbing resin is a resin comprising a copolymer of polyester and polyethylene glycol having polytetramethylene terephthalate as a main component, and the copolymerization amount of polyethylene glycol is 5 to 90% by weight, preferably 10 to 80% by weight. It is particularly preferably in the range of 30 to 60% by weight.
この共重合体の溶融粘度は特に制限はないが、常用のスパンボンド法やメルトブロー法にて繊維を得るためには、生産性の観点から、せん断速度1000秒-1での溶融粘度が100〜10000poiseの範囲のものを使用するのが好ましい。
吸水性不織布層に使用される繊維の繊度はその製造法によっても異なるが、0.01〜25dtex、特に0.05〜15dtexの範囲が適当である。
吸水性樹脂の溶融粘度がこの範囲であると、特にメルトブロー法による極細繊維化が容易であり、吸水性を有する極細繊維不織布を得ることができる。極細繊維の繊径は0.5〜5μmの範囲が好ましく、目付は1.0〜100g/m2 の範囲が可能であるが、低目付けの範囲(2〜10g/m2 )でも、安定した不織布が得られる。
The melt viscosity of this copolymer is not particularly limited, but in order to obtain fibers by a conventional spunbond method or melt blow method, from the viewpoint of productivity, the melt viscosity at a shear rate of 1000 sec- 1 is 100 to 100. It is preferable to use those in the range of 10,000 poise.
Although the fineness of the fiber used for the water-absorbing nonwoven fabric layer varies depending on the production method, a range of 0.01 to 25 dtex, particularly 0.05 to 15 dtex is appropriate.
When the melt viscosity of the water-absorbent resin is within this range, it is particularly easy to make ultrafine fibers by the melt blowing method, and an ultrafine fiber nonwoven fabric having water absorption can be obtained. The fine diameter of the ultrafine fiber is preferably in the range of 0.5 to 5 μm, and the basis weight can be in the range of 1.0 to 100 g / m 2 , but is stable even in the low basis weight range ( 2 to 10 g / m 2 ). A non-woven fabric is obtained.
〔熱可塑性繊維不織布層〕
熱可塑性不織布層を構成する樹脂としては、ポリエステル系ポリマー、ポリアミド系ポリマー、またはポリオレフィン系ポリマー、およびこれらのブレンド等を挙げることができる。
ポリオレフィン系ポリマーとしては、例えば、ポリプロピレン、低密度ポリエチレン、高密度ポリエチレン等を挙げることができる。ポリプロピレンに関しては、一般的なチーグラーナッタ触媒により合成されるものでもよいし、メタロセンに代表されるシングルサイト活性触媒により合成されたものであってもよい。ポリエチレンに関しては、直鎖状低密度ポリエチレン、低密度ポリエチレン、高密度ポリエチレン等を挙げることができる。更には、ポリプロピレンとポリエチレンとの共重合体やポリプロピレン中にポリエチレンやその他の添加剤を添加したポリマーであってもよい。
[Thermoplastic fiber nonwoven fabric layer]
Examples of the resin constituting the thermoplastic nonwoven fabric layer include polyester polymers, polyamide polymers, polyolefin polymers, and blends thereof.
Examples of the polyolefin-based polymer include polypropylene, low density polyethylene, and high density polyethylene. As for polypropylene, it may be synthesized by a general Ziegler-Natta catalyst or may be synthesized by a single site active catalyst typified by metallocene. Examples of polyethylene include linear low density polyethylene, low density polyethylene, and high density polyethylene. Furthermore, it may be a copolymer of polypropylene and polyethylene or a polymer obtained by adding polyethylene or other additives into polypropylene.
ポリアミド系ポリマーとしては、例えば、ナイロン4、ナイロン6、ナイロン46、ナイロン66、ナイロン11、ナイロン12、ナイロンMXD6(ポリメタキシレンアジパミド)等を挙げることができる。更には、これらのナイロンを主体とする共重合体あるいはこれらの混合物であってもよい。
ポリエステル系ポリマーとしては、例えば、ポリエチレンテレフタレート、ポリブチレ
ンテレフタレート、ポリトリメチレンテレフタレート、生分解性ポリエステル等を挙げることができる。更にはこれらのポリエステルを主体とする共重合体あるいはこれらの混合物であってもよい。
Examples of the polyamide polymer include nylon 4, nylon 6, nylon 46, nylon 66, nylon 11, nylon 12, nylon MXD6 (polymetaxylene adipamide), and the like. Furthermore, these nylon-based copolymers or a mixture thereof may be used.
Examples of the polyester-based polymer include polyethylene terephthalate, polybutylene terephthalate, polytrimethylene terephthalate, and biodegradable polyester. Furthermore, a copolymer mainly composed of these polyesters or a mixture thereof may be used.
また、熱可塑不織布層には本発明の目的を損なわない範囲で前記の吸水性樹脂を混合した混合繊維、あるいは吸水性樹脂との芯鞘、接合型の複合繊維を用いてもよい。
熱可塑性樹脂の溶融粘度は特に制限はないが、常用のスパンボンド法やメルトブロー法にて繊維を得るためには、生産性の観点から、せん断速度1000秒-1での溶融粘度が100〜10000poiseの範囲のものを使用するのが好ましい。
熱可塑性不織布層の繊維の繊度は0.05〜20dtex、好ましくは0.5〜15dtexの範囲が適当である。繊度が0.05dtex未満では十分な布の強度が得られない恐れがある。
The thermoplastic nonwoven fabric layer may be a mixed fiber in which the above water-absorbing resin is mixed, a core sheath with the water-absorbing resin, or a bonded composite fiber as long as the object of the present invention is not impaired.
The melt viscosity of the thermoplastic resin is not particularly limited, but in order to obtain fibers by a conventional spunbond method or melt blow method, the melt viscosity at a shear rate of 1000 sec- 1 is 100 to 10,000 poise from the viewpoint of productivity. It is preferable to use the thing of the range.
The fineness of the fibers of the thermoplastic nonwoven fabric layer is 0.05 to 20 dtex, preferably 0.5 to 15 dtex. If the fineness is less than 0.05 dtex, sufficient fabric strength may not be obtained.
また、本発明の吸水性繊維および熱可塑性繊維不織布層の繊維には、本発明の目的を損なわない範囲で、他の常用の各種添加成分、例えば、各種エラストマー類などの衝撃性改良材、結晶核剤、着色防止剤、ヒンダードフェノール、ヒンダードアミンなどの酸化防止剤、エチレンビスステアリルアミドや高級脂肪酸エステルなどの離型剤、ハロゲン化銅に代表される銅化合物などの耐熱剤、エポキシ化合物、可塑剤、滑剤、耐候剤、難燃剤、着色剤などの添加剤を添加することが出来る。
本発明において、吸水性繊維および熱可塑性不織布層の繊維の断面は、円形や楕円形、三角や四角等の多角形、扁平や中空等の異型断面形状でもよく、必要特性に応じて任意に設定することが出来る。
The fibers of the water-absorbent fiber and thermoplastic fiber nonwoven fabric layer of the present invention are not limited to the purpose of the present invention, and other commonly used additives such as impact modifiers such as various elastomers, crystals, etc. Nucleating agents, anti-coloring agents, antioxidants such as hindered phenols and hindered amines, mold release agents such as ethylenebisstearylamide and higher fatty acid esters, heat-resistant agents such as copper compounds typified by copper halides, epoxy compounds, plastics Additives such as agents, lubricants, weathering agents, flame retardants, and colorants can be added.
In the present invention, the cross section of the water-absorbing fiber and the thermoplastic nonwoven fabric layer may be a circular or elliptical shape, a polygonal shape such as a triangle or a square, or an irregular cross-sectional shape such as a flat shape or a hollow shape, and is arbitrarily set according to the required characteristics. I can do it.
〔吸水性不織布積層体〕
吸水性繊維の積層体への含有率は、1〜99重量%が好ましく、より好ましくは、10〜80重量%である。この比率が1重量%未満であると、吸水性を十分に発揮することができず好ましくない。逆に99重量%を超えると吸水性繊維の脱落や不織布積層体の強度が低下し、使用上の問題が生じるため好ましくない。この含有率は、積層体の用いられる用途特性、積層体としての強度と吸水性とのバランスを考慮して、最適条件を設定できる。
[Water-absorbing nonwoven fabric laminate]
As for the content rate to the laminated body of a water absorptive fiber, 1 to 99 weight% is preferable, More preferably, it is 10 to 80 weight%. If this ratio is less than 1% by weight, water absorption cannot be sufficiently exhibited, which is not preferable. On the other hand, if it exceeds 99% by weight, the water-absorbing fibers fall off and the strength of the nonwoven fabric laminate is lowered, which causes problems in use, which is not preferable. This content can be set to an optimum condition in consideration of the application characteristics of the laminate and the balance between strength and water absorption as the laminate.
本発明の吸水性不織布積層体は、公知の方法を用いて得られるものであり、製造方法、および積層方法としては従来公知の方法が任意に採用でき、特に制限はない。
吸水性不織布層、および熱可塑性樹脂からなる不織布層としては、短繊維あるいは長繊維のいずれを用いてもよく、その形成方法としても、スパンボンド法とメルトブロー法に代表される紡糸直結法や、カーディングやエアレイなどの乾式法、抄紙法などの湿式法などのいずれの方法を用いても良い。
The water-absorbent nonwoven fabric laminate of the present invention is obtained using a known method, and a conventionally known method can be arbitrarily employed as the production method and the lamination method, and there is no particular limitation.
As the nonwoven fabric layer made of a water-absorbing nonwoven fabric layer and a thermoplastic resin, either short fibers or long fibers may be used, and as a forming method thereof, a direct spinning method represented by a spunbond method and a melt blow method, Any method such as a dry method such as carding or airlaid, or a wet method such as papermaking may be used.
さらに、吸湿性繊維からなるウェブを熱可塑性樹脂からなる不織布層と接着あるいは絡み合わせる方法としても、カレンダー法、スルーエアヒーティング法などの熱的接着法、接着剤を用いて吸水性不織布層と熱可塑性樹脂からなる不織布層とを接着させる化学的接着法、ニードルパンチ法、水流交絡法、ステッチボンド法などの機械的接着法などのいずれの方法を用いても良い。
スパンボンド法、メルトブロー法及びこれらの積層により得られる不織布は、短繊維を経ることなく直接長繊維をウェブ化することにより作られるので、ボンディング部の破損による短繊維の脱落がないなどの物性上の特徴、及び生産性が高く、カード式短繊維不織布に比較して長所が多いため、衛生、土木、建築、農業・園芸、食品包材を中心に広範な用途で使用されており本発明の吸水性繊維からなる不織布積層体としては好適である。
Furthermore, as a method of adhering or entwining a web made of hygroscopic fibers with a nonwoven fabric layer made of a thermoplastic resin, a thermal bonding method such as a calender method or a through air heating method, and a water absorbent nonwoven fabric layer using an adhesive Any method such as a chemical bonding method for bonding a nonwoven fabric layer made of a thermoplastic resin, a needle punching method, a hydroentanglement method, a stitch bonding method, or the like may be used.
Non-woven fabrics obtained by the spunbond method, melt-blowing method, and lamination of these are made by directly forming long fibers without passing through the short fibers, so that the short fibers do not fall off due to breakage of the bonding part. It is used in a wide range of applications mainly in hygiene, civil engineering, architecture, agriculture / horticulture, and food packaging because it has high characteristics and productivity, and has many advantages over card-type short fiber nonwoven fabrics. It is suitable as a nonwoven fabric laminate comprising water-absorbing fibers.
本発明における不織布積層体の構造として、吸水性繊維からなる不織布層と熱可塑性樹
脂からなる基材が少なくとも各1層づつ積層されておればよく、積層するする層の数は特に限定されるものではないが、設備の制約や生産性を考慮した場合、3〜5層であることが好ましい。
さらには、両外層を熱可塑性樹脂からなる長繊維不織布で構成し、かつ中間層として吸水繊維からなる不織布層を配置した、3層以上の不織布がオンラインで積層してなる不織布積層体であることが好ましい。
As the structure of the nonwoven fabric laminate in the present invention, it is sufficient that a nonwoven fabric layer made of water-absorbing fibers and a base material made of a thermoplastic resin are laminated at least one layer each, and the number of layers to be laminated is particularly limited. However, it is preferable that the number of layers is 3 to 5 in consideration of equipment restrictions and productivity.
Furthermore, it is a nonwoven fabric laminate in which both outer layers are composed of a long-fiber nonwoven fabric made of a thermoplastic resin, and a nonwoven fabric layer made of water-absorbing fibers is arranged as an intermediate layer, and three or more layers of nonwoven fabric are laminated online. Is preferred.
このような構造を採用することにより、中間層に含まれる吸水繊維が優れた吸水性を示すと同時に、吸水性繊維の脱落と、湿潤時の布強度の低下を、低減することができる、積層体構成として適している。
オンライン上で、上記のような3層積層構造を形成すると、積層による吸水繊維の外層への突き出し効果が発生しやすくなり、より吸水速度を更に向上させることが可能となる。その際、吸水繊維の積層体全重量に占める割合が5〜70%であることが、湿潤時の強度低下を防ぐ上で好ましい。
By adopting such a structure, the water-absorbing fibers contained in the intermediate layer exhibit excellent water absorption, and at the same time, the dropping of water-absorbing fibers and the decrease in fabric strength when wet can be reduced. Suitable for body composition.
When a three-layer laminated structure as described above is formed online, the effect of protruding water-absorbing fibers to the outer layer due to the lamination tends to occur, and the water absorption rate can be further improved. At that time, it is preferable that the ratio of the water-absorbing fibers to the total weight of the laminate is 5 to 70% in order to prevent the strength from being reduced when wet.
本件発明の好ましい態様として、吸水性不織布が、熱可塑性樹脂からなるスパンボンド不織布を移動するウェブ捕集面上堆積させ(S層)、その上にメルトブローン法によって形成される吸水性繊維を直接堆積させ(M層)、さらにその上に熱可塑性樹脂からなるスパンボンド不織布を直接堆積させて(S層)、熱エンボス処理により、積層体が圧着さてれなる吸水性不織布積層体が挙げられる。このようなSMS構造の不織布のM層に、吸水性不織布を用いると、M層での吸水性の確保、S層による強度保持、耐磨耗性性の向上、毛羽たちの防止、柔軟風合い等、M層とS層の相乗効果が発揮され、好ましい積層不織布が得られる。該積層不織布は、用途に合わせて、適宜、層の数を調整できる。
吸水性繊維からなる不織布と、疎水性繊維からなる不織布を熱圧着で積層一体化することで、吸水、保水、拡散、放湿などの組み合わせ作用を有する不織布を得る可能性を有している。
As a preferred embodiment of the present invention, a water-absorbing nonwoven fabric is deposited on a web collecting surface on which a spunbond nonwoven fabric made of a thermoplastic resin is moved (S layer), and water-absorbing fibers formed by a melt blown method are directly deposited thereon. (M layer), a spunbond nonwoven fabric made of a thermoplastic resin is directly deposited thereon (S layer), and a water-absorbent nonwoven fabric laminate in which the laminate is pressure-bonded by heat embossing treatment can be mentioned. If a water-absorbing nonwoven fabric is used for the M layer of such an SMS-structured nonwoven fabric, water absorption in the M layer is ensured, strength retention by the S layer, improved wear resistance, fluff prevention, soft texture, etc. A synergistic effect of the M layer and the S layer is exhibited, and a preferable laminated nonwoven fabric is obtained. The number of layers of the laminated nonwoven fabric can be adjusted appropriately according to the application.
There is a possibility of obtaining a nonwoven fabric having a combined action of water absorption, water retention, diffusion, moisture release, etc., by laminating and integrating a nonwoven fabric made of water-absorbing fibers and a nonwoven fabric made of hydrophobic fibers by thermocompression bonding.
例えば、以下の様な方法で得られる。
熱可塑吸水性不織布および熱可塑性樹脂からなる不織布層の繊維形成には、通常使用される紡糸口金を用いて溶融紡糸をすればよい。紡糸した糸条は、冷却した後に延伸しウェブをコンベア上で捕集し任意の方法により布帛とする。
さらに、本発明の吸水性不織布積層体には、本発明の目的を損なわない範囲で、他の常用の後加工、例えば、難燃剤、消臭剤、抗菌剤、防ダニ剤などの付与をしてもよいし、染色、撥水加工などを施してもよい。
また、本発明の吸水性不織布積層体の形状、形態、目付等についても、必要特性に応じて任意に設定することが出来る。
吸水性不織布積層体に、印刷、染色、コーティング加工などを施すことも可能であるし、種類の異なる素材、製法、製品を複合化しても何ら差し支えない。
For example, it can be obtained by the following method.
For fiber formation of a nonwoven fabric layer composed of a thermoplastic water-absorbing nonwoven fabric and a thermoplastic resin, melt spinning may be performed using a commonly used spinneret. The spun yarn is cooled and then stretched, and the web is collected on a conveyor to obtain a fabric by an arbitrary method.
Further, the water-absorbent nonwoven fabric laminate of the present invention is provided with other conventional post-processing, for example, flame retardant, deodorant, antibacterial agent, anti-mite agent, etc., within the range not impairing the object of the present invention. Alternatively, dyeing, water-repellent processing, or the like may be performed.
Further, the shape, form, basis weight, etc. of the water-absorbent nonwoven fabric laminate of the present invention can be arbitrarily set according to the required characteristics.
The water-absorbing nonwoven fabric laminate can be subjected to printing, dyeing, coating processing, etc., and different types of materials, manufacturing methods and products can be combined.
本発明の吸水性不織布積層体は、従来の吸水性材料が用いられている用途に広く使用可能である。例えば、衣料部材、ディスポ衣料、靴部材などの衣料用途、保護衣、防護用品などの防護用途、手術着、マスク、ハップ剤基布などの医療用途、ルーフィング、タフト・カーペット基布、結露防止シートなどの建築用途、補強材、保護材、地中埋設管の補修材などの土木用途、自動車内装、自動車部品などの車両用途、救急用品、洗浄用品、おしぼりなどの衛生用途、カーペット、家具部材、壁紙などの家具・インテリア用途、ウェットワイパー、クリーニング材などのワイパー用途、空気フィルター、バグフィルター、エレクトレットフィルターなどのフィルター用途、布団、布団袋、枕カバーなどの寝装用途、べた掛けシート、防草シート、園芸プランターなどの農業・園芸用途、人工皮革用基布、合成皮革用基布、塩ビレザー用基布などの人工皮革類の基布用途、収納用品、食品等の包装資材、台所用品などの生活資材用途、電気材料、製品材料、機器部材などの工業資材
用途などである。
The water-absorbing nonwoven fabric laminate of the present invention can be widely used in applications where conventional water-absorbing materials are used. For example, apparel materials such as apparel materials, disposable apparel, and shoe materials, protective apparel such as protective clothing, protective equipment, medical uses such as surgical gowns, masks, haptic base fabrics, roofing, tufted carpet base fabrics, anti-condensation sheets Architectural applications such as, reinforcing materials, protective materials, civil engineering applications such as underground pipe repair materials, automotive interiors, vehicle applications such as automobile parts, sanitary applications such as emergency supplies, cleaning products, and hand towels, carpets, furniture components, Furniture and interior applications such as wallpaper, wipers such as wet wipers and cleaning materials, filter applications such as air filters, bag filters, electret filters, bedding applications such as futons, futon bags, pillow covers, solid sheets, grass protection Agricultural / horticultural applications such as seats, garden planters, artificial leather base fabrics, synthetic leather base fabrics, PVC leather base fabrics Of artificial leather such base fabric applications, storage supplies, packaging materials such as foods, living materials applications such as kitchen utensils, electrical material, or the like industrial materials applications such as product material, equipment member.
以下に、実施例などにより本発明をさらに具体的に説明するが、本発明はこれら実施例などにより何ら限定されるものではない。
なお、測定方法、評価方法等は下記の通りである。
<引張強さ>
JIS−L−1096の4.3に示された方法で測定して引張強さを評価した。
<吸水速度>
JIS−L−1096の6.26.1滴下法に示された方法で測定し、吸水に要した秒数で、吸水速度を評価した。
Hereinafter, the present invention will be described more specifically with reference to examples and the like, but the present invention is not limited to these examples.
Measurement methods, evaluation methods, etc. are as follows.
<Tensile strength>
Tensile strength was evaluated by measurement according to JIS-L-1096 4.3.
<Water absorption speed>
It measured by the method shown by 6.26.1 dropping method of JIS-L-1096, and the water absorption speed was evaluated by the number of seconds required for water absorption.
<不織布の保水率>
下記式(1)で示す吸水率で不織布の保水性を評価した。
まず、試料を温度20℃、相対湿度65%の雰囲気中で24時間調湿して重量W1(g)を測定し、次に温度20℃の水道水中に24時間浸漬した後取り出し、遠心脱水機にて3500rpmで5分間脱水後、重量W2(g)を測定し、下記式(1)で保水率T0(重量%)を求めた。
保水率T0(重量%)=〔(W2−W1)/W1〕×100(1)
<ポリエステルの固有粘度>
オルトクロロフェノールを溶媒とし、試料濃度1g/100cc、温度35℃の条件で定法により測定した。
<Water retention rate of nonwoven fabric>
The water retention of the nonwoven fabric was evaluated based on the water absorption represented by the following formula (1).
First, the sample was conditioned at a temperature of 20 ° C. and a relative humidity of 65% for 24 hours to measure the weight W1 (g), then immersed in tap water at a temperature of 20 ° C. for 24 hours, taken out, and centrifuged. After dehydration at 3500 rpm for 5 minutes, the weight W2 (g) was measured, and the water retention rate T0 (% by weight) was determined by the following formula (1).
Water retention rate T0 (% by weight) = [(W2-W1) / W1] × 100 (1)
<Intrinsic viscosity of polyester>
Measurement was carried out by a conventional method using orthochlorophenol as a solvent and a sample concentration of 1 g / 100 cc and a temperature of 35 ° C.
<メルトフローレート>
JIS−K−7210に記載の方法に準じてメルトフローレート(MFR)を測定した。
<ポリアミドの相対粘度>
濃度97%の硫酸を溶媒とし、試料濃度1g/100cc、温度25℃の条件で定法により測定した。
<Melt flow rate>
The melt flow rate (MFR) was measured according to the method described in JIS-K-7210.
<Relative viscosity of polyamide>
Measurement was carried out by a conventional method under the conditions of a sample concentration of 1 g / 100 cc and a temperature of 25 ° C. using sulfuric acid having a concentration of 97% as a solvent.
[実施例1]
MFRが40のポリプロピレン樹脂(PP)を常用のスパンボンド溶融紡糸装置に供給し、230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3000m/分にて引き取り、2.2dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が7.5g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートを主成分とするポリエステルとポリエチレングリコールとの共重合ポリエステル樹脂を、常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金からメルトブロー溶融紡出して2.5μmの吸水性繊維からなる目付が2g/m2 のウェブを得た。
[Example 1]
A polypropylene resin (PP) having an MFR of 40 is supplied to a conventional spunbond melt spinning apparatus, melted and mixed uniformly at 230 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 3000 m / min. To obtain a 2.2 dtex polypropylene fiber. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 7.5 g / m 2 .
Next, a polyester resin composed of polytetramethylene terephthalate, which has an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight, and polyethylene glycol is supplied to a conventional melt blow melt spinning apparatus. The mixture was uniformly melt-mixed at 270 ° C. and melt blown from a spinneret having a spinning hole having a circular cross section to obtain a web having a basis weight of 2 g / m 2 made of 2.5 μm water-absorbing fibers.
得られた吸水性繊維からなるウェブを目付が7.5g/m2 のポリプロピレンからウェブで挟み、135℃に加熱したピンポイントエンボス(圧着面積率7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して17g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。吸水性繊維の含有比率は12%であり、後述の比較例1と対して、強度は同一であり、吸水速度は早くなり、保水率は比較例1の約3倍に増加し、保水性が大幅に向上した。 A linear pressure between a pinpoint embossing (crimping area ratio 7.1%) roll and a flat roll, which is obtained by sandwiching a web made of water-absorbing fibers from polypropylene having a basis weight of 7.5 g / m 2 and heating to 135 ° C. A 17 g / m 2 nonwoven fabric was prepared by partial thermocompression bonding at 45 N / cm. Table 1 shows the physical properties of the obtained nonwoven fabric. The content ratio of the water-absorbing fiber is 12%, the strength is the same as that of Comparative Example 1 described later, the water absorption speed is increased, the water retention rate is increased about 3 times that of Comparative Example 1, and the water retention is increased. Greatly improved.
[実施例2]
MFR40のポリプロピレン樹脂(PP)を常用の溶融紡糸装置に供給し230℃にて
均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3200m/分にて引き取り、2.7dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が15g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水吸湿性繊維からなる目付が5g/m2 の吸水性ウェブを得た。
[Example 2]
1. MFR40 polypropylene resin (PP) is supplied to a conventional melt spinning apparatus, melted and mixed uniformly at 230 ° C., melt spun from a spinneret having a spinning hole having a circular cross section, and taken up at a speed of 3200 m / min. 7 dtex polypropylene fiber was obtained. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 15 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole having a circular cross section to obtain a water-absorbing web having a basis weight of 5 g / m 2 made of water-absorbing and hygroscopic fibers of 2.5 μm.
得られた吸水性ウェブと目付が15g/m2 のポリプロピレンウェブとを135℃に加熱したピンポイントエンボス(圧着面積率7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して20g/m2 の不織布を成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例2と対して、強度はやや低下したが、吸水速度は30秒と早くなり、保水率は、比較例2の約7倍に増加し、保水性が大幅に向上した。本実施例では、強度を維持しながら、大幅な吸水特性の改善が見られた。
Partial heat at a linear pressure of 45 N / cm between a pinpoint embossed (crimp area ratio 7.1%) roll obtained by heating the water-absorbent web and a polypropylene web having a basis weight of 15 g / m 2 to 135 ° C. and a flat roll. A nonwoven fabric of 20 g / m 2 was formed by pressure bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 25%, and the strength is slightly lower than that of Comparative Example 2 described later, but the water absorption speed is as fast as 30 seconds, and the water retention rate is about 7 times that of Comparative Example 2. The water retention was greatly improved. In this example, the water absorption characteristics were significantly improved while maintaining the strength.
[実施例3]
MFRが40のポリプロピレン樹脂(PP)を常用の溶融紡糸装置に供給し230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3000m/分にて引き取り、2.2dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が10g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートを主成分とするポリエステルとポリエチレングリコールとの共重合ポリエステル樹脂を常用の溶融紡糸装置に供給し、230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して3.0dtexの吸水性繊維からなる目付が10g/m2 のウェブを得た。
[Example 3]
A polypropylene resin (PP) having an MFR of 40 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 230 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and taken up at a speed of 3000 m / min. A 2.2 dtex polypropylene fiber was obtained. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 10 g / m 2 .
Next, a polyester resin having a polytetramethylene terephthalate as a main component and an intrinsic viscosity of 0.92 and a copolymerization ratio of polyethylene glycol of 45% by weight is supplied to a conventional melt spinning apparatus, The mixture was uniformly melt-mixed at 230 ° C., and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web having a basis weight of 10 g / m 2 made of 3.0 dtex water-absorbing fibers.
得られた吸水性繊維からなるウェブと目付が10g/m2 のポリプロピレンウェブとを135℃に加熱したピンポイントエンボス(圧着面積率7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して20g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は50%であり、後述の比較例2と対して、強度はやや低下したが、吸水速度は早くなり、保水率は、比較例2の約13倍に増加し、保水性が大幅に向上した。本実施例では、強度はやや低下したが、大幅な吸水特性の改善が見られた。
A linear pressure of 45 N / cm between a pinpoint embossing (crimping area ratio of 7.1%) roll obtained by heating a web made of water-absorbing fibers and a polypropylene web having a basis weight of 10 g / m 2 to 135 ° C. and a flat roll. And 20 g / m 2 nonwoven fabric was prepared by partial thermocompression bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 50%, and the strength is slightly reduced as compared with Comparative Example 2 described later, but the water absorption speed is increased, and the water retention rate is increased to about 13 times that of Comparative Example 2, and the water retention rate is increased. The characteristics have been greatly improved. In this example, the strength slightly decreased, but a significant improvement in water absorption characteristics was observed.
[実施例4]
MFRが40のポリプロピレン樹脂(PP)を常用のスパンボンド溶融紡糸装置に供給し230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3000m/分にて引き取り、2.2dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が7.5g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートを主成分とするポリエステルとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が2g/m2 のウェブを得た。
[Example 4]
A polypropylene resin (PP) having an MFR of 40 is supplied to a conventional spunbond melt spinning apparatus, melted and mixed uniformly at 230 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 3000 m / min. Taking up, a 2.2 dtex polypropylene fiber was obtained. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 7.5 g / m 2 .
Next, a polyester resin having a polytetramethylene terephthalate main component and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus. The mixture was uniformly melt-mixed at 270 ° C., and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web having a basis weight of 2 g / m 2 made of 2.5 μm water-absorbing fibers.
得られた吸水性繊維からなるウェブを目付が7.5g/m2 のポリプロピレンからなるウェブで挟み、ノズル径0.15mm、ノズルピッチ0.8mm、列数2列のノズルから水圧50kg/cm2 の柱状流を噴射し、水流交絡処理を行い17g/m2 の不織布を作
成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は12%であり、後述の比較例1と対して、強度は同一レベルであり、吸水速度は早くなり、保水率は比較例1の約3倍に増加し、保水性が大幅に向上した。
The obtained web made of water-absorbing fibers was sandwiched between webs made of polypropylene having a basis weight of 7.5 g / m 2 , and the water pressure was 50 kg / cm 2 from nozzles having a nozzle diameter of 0.15 mm, a nozzle pitch of 0.8 mm, and two rows. A columnar flow was sprayed and subjected to hydroentanglement treatment to produce a nonwoven fabric of 17 g / m 2 . Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 12%, and the strength is the same level as that of Comparative Example 1 described later, the water absorption speed is increased, and the water retention rate is increased about three times that of Comparative Example 1, and the water retention rate is increased. There has been a significant improvement.
[実施例5]
MFRが40のポリプロピレン樹脂(PP)を常用のスパンボンド溶融紡糸装置に供給し230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3000m/分にて引き取り、2.2dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が7.5g/m2 のウェブを形成した。
[Example 5]
A polypropylene resin (PP) having an MFR of 40 is supplied to a conventional spunbond melt spinning apparatus, melted and mixed uniformly at 230 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 3000 m / min. Taking up, a 2.2 dtex polypropylene fiber was obtained. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 7.5 g / m 2 .
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートを主成分とするポリエステルとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が2g/m2 のウェブを得た。 Next, a polyester resin having a polytetramethylene terephthalate main component and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus. The mixture was uniformly melt-mixed at 270 ° C., and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web having a basis weight of 2 g / m 2 made of 2.5 μm water-absorbing fibers.
得られた吸水性繊維からなるウェブを目付が7.5g/m2のポリプロピレンからなるウェブで挟みパンチング密度が10個/cm2、ニードルの突き込み深さ10mmでニードルパンチ処理を行い17g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は12%であり、後述の比較例1と対して、強度は同一レベルであり、吸水速度は早くなり、保水率は比較例1の約3倍に増加し、保水性が大幅に向上した。
The obtained web made of water-absorbing fibers was sandwiched between polypropylene webs having a basis weight of 7.5 g / m 2 , punching density was 10 pieces / cm 2 , and needle punching was performed at a needle penetration depth of 10 mm, and 17 g / m. Two nonwoven fabrics were made. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 12%, and the strength is the same level as that of Comparative Example 1 described later, the water absorption speed is increased, and the water retention rate is increased about three times that of Comparative Example 1, and the water retention rate is increased. There has been a significant improvement.
[実施例6]
相対粘度が2.5のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が15g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水吸湿性繊維からなる目付が10g/m2 のウェブを得た。
[Example 6]
Nylon 6 resin (N6) having a relative viscosity of 2.5 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The obtained nylon 6 fiber was spread and dispersed to form a web having a basis weight of 15 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web made of 2.5 μm water-absorbing and hygroscopic fibers with a basis weight of 10 g / m 2 .
得られた吸水吸放湿性ウェブを目付が15g/m2 のナイロン6繊維からなるウェブで挟み、165℃に加熱したピンポイントエンボス(圧着面積率7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して40g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例3と対して、強度はほぼ同一レベルであり、吸水速度は早くなり、保水率は比較例3の約2倍に増加し、保水性が大幅に向上した。本実施例では、強度を維持しながら、大幅な吸水特性の改善が見られた。
The resulting water-absorbing / absorbing / releasing web was sandwiched between nylon 6 fibers having a basis weight of 15 g / m 2 and heated to 165 ° C. Linear pressure between a pinpoint embossed (crimp area ratio 7.1%) roll and a flat roll A 40 g / m 2 non-woven fabric was prepared by partial thermocompression bonding at 45 N / cm. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 25%, and the strength is almost the same level as that of Comparative Example 3 described later, the water absorption speed is increased, and the water retention rate is increased approximately twice that of Comparative Example 3, The characteristics have been greatly improved. In this example, the water absorption characteristics were significantly improved while maintaining the strength.
[実施例7]
相対粘度が2.5のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が20g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリ
テトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水吸湿性繊維からなる目付が20g/m2 の吸水性ウェブを得た。
[Example 7]
Nylon 6 resin (N6) having a relative viscosity of 2.5 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The obtained nylon 6 fiber was spread and dispersed to form a web having a basis weight of 20 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole having a circular cross section to obtain a water-absorbing web having a basis weight of 20 g / m 2 made of water-absorbing and hygroscopic fibers of 2.5 μm.
得られた吸水性ウェブと目付が20g/m2 のナイロン6繊維からなるウェブを165℃に加熱したピンポイントエンボス(圧着面積率7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して40g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は50%であり、後述の比較例3と対して、強度はやや低下したが、吸水速度は早くなり、保水率は比較例3の約4倍に増加し、保水性が大幅に向上した。本実施例では、強度はやや低下したが、大幅な吸水特性の改善が見られた。
The obtained water-absorbing web and a web made of nylon 6 fibers having a basis weight of 20 g / m 2 were heated to 165 ° C., and the linear pressure was 45 N / cm between the pinpoint embossed (crimping area ratio 7.1%) roll and the flat roll. A 40 g / m 2 nonwoven fabric was prepared by partial thermocompression bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber was 50%, and the strength was slightly reduced as compared with Comparative Example 3 described later, but the water absorption rate was increased and the water retention rate was increased about 4 times that of Comparative Example 3, and the water retention rate was increased. There has been a significant improvement. In this example, the strength slightly decreased, but a significant improvement in water absorption characteristics was observed.
[実施例8]
相対粘度が2.5のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が20g/m2 のウェブを形成した。
[Example 8]
Nylon 6 resin (N6) having a relative viscosity of 2.5 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The obtained nylon 6 fiber was spread and dispersed to form a web having a basis weight of 20 g / m 2 .
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用の溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して3.0dtexの吸水吸湿性繊維からなる目付が20g/m2 の吸水性ウェブを得た。得られた吸水性ウェブと目付が20g/m2のナイロン6繊維からなるウェブを165℃に加熱したピンポイントエンボス(圧着面積率7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して40g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は50%であり、後述の比較例3と対して、強度はやや低下したが、吸水速度は早くなり、保水率は比較例3の約4倍に増加し、保水性が大幅に向上した。本実施例では、強度はやや低下したが、大幅な吸水特性の改善が見られた。
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt spinning apparatus and uniformly distributed at 270 ° C. The mixture was melt-mixed and melt-spun from a spinneret having a spinning hole having a circular cross section to obtain a water-absorbing web having a basis weight of 20 g / m 2 made of water-absorbing and hygroscopic fibers of 3.0 dtex. The obtained water-absorbing web and a web made of nylon 6 fibers having a basis weight of 20 g / m 2 were heated to 165 ° C., and the linear pressure was 45 N / cm between the pinpoint embossed (crimping area ratio 7.1%) roll and the flat roll. A 40 g / m 2 nonwoven fabric was prepared by partial thermocompression bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber was 50%, and the strength was slightly reduced as compared with Comparative Example 3 described later, but the water absorption rate was increased and the water retention rate was increased about 4 times that of Comparative Example 3, and the water retention rate was increased. There has been a significant improvement. In this example, the strength slightly decreased, but a significant improvement in water absorption characteristics was observed.
[実施例9]
相対粘度が2.5のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が15g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水吸湿性繊維からなる目付が10g/m2 のウェブを得た。
[Example 9]
Nylon 6 resin (N6) having a relative viscosity of 2.5 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The obtained nylon 6 fiber was spread and dispersed to form a web having a basis weight of 15 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web made of 2.5 μm water-absorbing and hygroscopic fibers with a basis weight of 10 g / m 2 .
得られた吸水吸放湿性ウェブを目付が15g/m2 のナイロン6繊維からなるウェブで挟み、ノズル径0.15mm、ノズルピッチ0.8mm、列数2列のノズルから水圧50kg/cm2 の柱状流を噴射し、水流交絡処理を行い40g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例3と対して、強度はほぼ同一レベルであり、吸水速度は早くなり、保水率は比較例3の約2倍に増加し、保水性が大幅に向上した。本実施例では、強度は損なうことなく、大幅な吸水特性の改善が見られた。
The obtained water-absorbing and moisture-releasing web is sandwiched between nylon 6 fibers having a basis weight of 15 g / m 2 , a nozzle diameter of 0.15 mm, a nozzle pitch of 0.8 mm, and a water pressure of 50 kg / cm 2 from two rows of nozzles. A columnar flow was sprayed and subjected to hydroentanglement treatment to produce a 40 g / m 2 nonwoven fabric. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 25%, and the strength is almost the same level as that of Comparative Example 3 described later, the water absorption speed is increased, and the water retention rate is increased approximately twice that of Comparative Example 3, The characteristics have been greatly improved. In this example, significant improvement in water absorption characteristics was observed without losing strength.
[実施例10]
相対粘度が2.5のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が15g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水吸湿性繊維からなる目付が10g/m2 のウェブを得た。
[Example 10]
Nylon 6 resin (N6) having a relative viscosity of 2.5 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The obtained nylon 6 fiber was spread and dispersed to form a web having a basis weight of 15 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web made of 2.5 μm water-absorbing and hygroscopic fibers with a basis weight of 10 g / m 2 .
得られた吸水吸放湿性ウェブを目付が15g/m2 のナイロン6繊維からなるウェブで挟み、パンチング密度が10個/cm2、ニードルの突き込み深さ10mmでニードルパンチ処理を行い40g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例3と対して、強度はほぼ同一れべるであり、吸水速度は早くなり、保水率は比較例3の約2倍に増加し、保水性が大幅に向上した。本実施例では、強度は損なうことなく、大幅な吸水特性の改善が見られた。
The obtained water-absorbing / releasing moisture-absorbing web is sandwiched between nylon 6 fibers having a basis weight of 15 g / m 2 and subjected to a needle punching process with a punching density of 10 pieces / cm 2 and a needle penetration depth of 10 mm. Two nonwoven fabrics were made. Table 1 shows the physical properties of the obtained nonwoven fabric.
The content ratio of the water-absorbing fiber is 25%, and the strength is almost the same as that of Comparative Example 3 to be described later, the water absorption speed is increased, and the water retention rate is increased about twice that of Comparative Example 3. The water retention was greatly improved. In this example, significant improvement in water absorption characteristics was observed without losing strength.
[実施例11]
固有粘度が0.70のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が30g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が20g/m2 のウェブを得た。
[Example 11]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.70 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 30 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web having a weight per unit area of 20 g / m 2 made of water-absorbing fibers of 2.5 μm.
得られた吸水性ウェブを目付が30g/m2 のポリエチレンテレフタレート繊維からなるウェブで挟み、165℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して80g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例5に対して、強度はほぼ同一であり、吸水速度は大幅に早くなり、保水率は比較例5の約5倍の31%に増加し、保水性が大幅に向上した。本実施例では、強度を損なうことなく、大幅な吸水特性の改善が見られた。
The obtained water-absorbing web was sandwiched between polyethylene terephthalate fibers having a basis weight of 30 g / m 2 and heated to 165 ° C. between a rectangular pattern embossed (crimp area 11.4%) roll and a flat roll at a linear pressure of 45 N / cm. A non-woven fabric of 80 g / m 2 was prepared by partial thermocompression bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 25%, the strength is almost the same as that of Comparative Example 5 described later, the water absorption rate is significantly faster, and the water retention rate is 31%, which is about 5 times that of Comparative Example 5. The water retention was greatly improved. In this example, significant improvement in water absorption characteristics was observed without impairing strength.
[実施例12]
固有粘度が0.70のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が15g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が30g
/m2 の吸水吸放湿性ウェブを得た。
[Example 12]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.70 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 15 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. 30 g of basis weight made of 2.5 μm water-absorbing fibers melt-spun from a spinneret having a spinning hole with a circular cross section
A water-absorbing / releasing moisture-absorbing web having an area of m 2 was obtained.
得られた吸水吸放湿性ウェブを目付が15g/m2 のポリエチレンテレフタレート繊維からなるウェブで挟み、165℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して60g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は50%であり、後述の比較例6に対して、吸水速度は2.8秒と大幅に早くなり、保水率は比較例6の約8倍の47%に増加し、保水性が大幅に向上した。
The resulting water-absorbing / absorbing / releasing web was sandwiched between polyethylene terephthalate fibers having a basis weight of 15 g / m 2 and heated to 165 ° C. between a rectangular pattern embossed (crimp area 11.4%) roll and a flat roll with a linear pressure of 45 N A non-woven fabric of 60 g / m 2 was prepared by partial thermocompression bonding at / cm. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 50%. Compared to Comparative Example 6 described later, the water absorption speed is 2.8 seconds, and the water retention rate increases to 47%, which is about 8 times that of Comparative Example 6. The water retention was greatly improved.
[実施例13]
固有粘度が0.70のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が10g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が60g/m2 のウェブを得た。
[Example 13]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.70 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 10 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt-spun from a spinneret having a spinning hole having a circular cross-section to obtain a web having a basis weight of 60 g / m 2 made of 2.5 μm water-absorbing fibers.
得られた吸水吸放湿性ウェブを目付が10g/m2 のポリエチレンテレフタレート繊維からなるウェブで挟み、165℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して80g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は75%であり、後述の比較例6に対して、吸水速度は0.8秒と大幅に早くなり、保水率は比較例6の約10倍の65%に増加し、保水性が大幅に向上した。
The obtained water-absorbing and moisture-releasing web was sandwiched between polyethylene terephthalate fibers having a basis weight of 10 g / m 2 and heated to 165 ° C. between a rectangular pattern embossed (crimp area 11.4%) roll and a flat roll with a linear pressure of 45 N A non-woven fabric of 80 g / m 2 was prepared by partial thermocompression bonding at / cm. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 75%. Compared to Comparative Example 6 described later, the water absorption speed is significantly faster at 0.8 seconds, and the water retention rate is increased to about 10% of Comparative Example 6 to 65%. The water retention was greatly improved.
[実施例14]
固有粘度が0.70のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が30g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が10g/m2 のウェブを得た。
[Example 14]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.70 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 30 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web having a basis weight of 10 g / m 2 made of 2.5 μm water-absorbing fibers.
得られた吸水性ウェブと目付が30g/m2 のポリエチレンテレフタレート繊維からなるウェブを165℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して60g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は50%であり、後述の比較例6に対して、吸水速度は0.8秒と大幅に早くなり、保水率は比較例6の約8倍の48%に増加し、保水性が大幅に向上した。
The obtained water-absorbing web and a web made of polyethylene terephthalate fibers having a basis weight of 30 g / m 2 were heated at 165 ° C. between a rectangular pattern embossed (crimp area 11.4%) roll and a flat roll at a linear pressure of 45 N / cm. A non-woven fabric of 60 g / m 2 was prepared by partial thermocompression bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 50%, and the water absorption rate is significantly faster at 0.8 seconds than Comparative Example 6 described later, and the water retention rate increases to 48%, about 8 times that of Comparative Example 6. The water retention was greatly improved.
[実施例15]
固有粘度が0.77のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が30g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用の溶融紡糸装置に供給し、230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して3.0dtexの吸水性繊維からなる目付が30g/m2 のウェブを得た。
[Example 15]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.77 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 30 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt spinning apparatus and uniformly distributed at 230 ° C. The mixture was melt-mixed and melt-spun from a spinneret having a spinning hole with a circular cross section to obtain a web made of 3.0 dtex water-absorbing fibers with a basis weight of 30 g / m 2 .
得られた吸水性ウェブを目付が30g/m2 のポリエチレンテレフタレート繊維からなるウェブを165℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して60g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は50%であり、後述の比較例6に対して、吸水速度は0.8秒と大幅に早くなり、保水率は比較例6の約8倍の48%に増加し、保水性が大幅に向上した。
The resulting water-absorbing web was formed of a polyethylene terephthalate fiber having a basis weight of 30 g / m 2 and heated to 165 ° C. between a rectangular embossed (crimp area 11.4%) roll and a flat roll at a linear pressure of 45 N / cm. A non-woven fabric of 60 g / m 2 was prepared by partial thermocompression bonding. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 50%, and the water absorption rate is significantly faster at 0.8 seconds than Comparative Example 6 described later, and the water retention rate increases to 48%, about 8 times that of Comparative Example 6. The water retention was greatly improved.
[実施例16]
固有粘度が0.70のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が30g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が20g/m2 のウェブを得た。
[Example 16]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.70 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 30 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. The mixture was melt-mixed and melt spun from a spinneret having a spinning hole with a circular cross section to obtain a web having a weight per unit area of 20 g / m 2 made of water-absorbing fibers of 2.5 μm.
得られた吸水性ウェブを目付が30g/m2 のポリエチレンテレフタレート繊維からなるウェブで挟み、ノズル径0.15mm、ノズルピッチ0.8mm、列数2列のノズルから水圧50kg/cm2 の柱状流を噴射し、水流交絡処理を行い80g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例5に対して、強度はやや増加し、吸水速度は10秒と大幅に早くなり、保水率は比較例5の約5倍に増加し、保水性が大幅に向上した。
The obtained water-absorbing web was sandwiched between webs made of polyethylene terephthalate fibers having a basis weight of 30 g / m 2 , and a columnar flow having a nozzle diameter of 0.15 mm, a nozzle pitch of 0.8 mm, and a water pressure of 50 kg / cm 2 from two nozzles. Were sprayed and subjected to hydroentanglement treatment to prepare an 80 g / m 2 nonwoven fabric. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 25%, the strength is slightly increased compared to Comparative Example 5 described later, the water absorption speed is significantly faster, 10 seconds, and the water retention rate is about 5 times that of Comparative Example 5. The water retention was greatly improved.
[実施例17]
固有粘度が0.70のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が30g/m2 のウェブを形成した。
次に固有粘度が0.92でポリエチレングリコールの共重合率が45重量%であるポリテトラメチレンテレフタレートとポリエチレングリコールとの共重合ポリエステル樹脂を常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmの吸水性繊維からなる目付が20g
/m2 の吸水性ウェブを得た。
[Example 17]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.70 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 30 g / m 2 .
Next, a copolyester resin of polytetramethylene terephthalate and polyethylene glycol having an intrinsic viscosity of 0.92 and a polyethylene glycol copolymerization ratio of 45% by weight is supplied to a conventional melt blow melt spinning apparatus, and uniform at 270 ° C. Is melt-spun from a spinneret having a spinning hole having a circular cross section, and a basis weight of 2.5 g of water-absorbing fiber is 20 g.
A water-absorbing web of / m 2 was obtained.
得られた吸水性ウェブを目付が30g/m2 のポリエチレンテレフタレート繊維からなるウェブで挟み、パンチング密度が10個/cm2、ニードルの突き込み深さ10mmで、ニードルパンチ処理を行い80g/m2 の不織布を作成した。得られた不織布の各物性を表1に示す。
吸水性繊維の含有比率は25%であり、後述の比較例5に対して、強度はやや増加し、吸水速度は10秒と大幅に早くなり、保水率は比較例5の約5倍に増加し、保水性が大幅に向上した。
The obtained water-absorbing web was sandwiched between polyethylene terephthalate fibers having a basis weight of 30 g / m 2 , punching density was 10 pieces / cm 2 , needle penetration depth was 10 mm, and needle punching was performed to give 80 g / m 2. A non-woven fabric was prepared. Table 1 shows the physical properties of the obtained nonwoven fabric.
The water-absorbing fiber content is 25%, the strength is slightly increased compared to Comparative Example 5 described later, the water absorption speed is significantly faster, 10 seconds, and the water retention rate is about 5 times that of Comparative Example 5. The water retention was greatly improved.
[比較例1]
MFR40のポリプロピレン樹脂(PP)を常用の溶融紡糸装置に供給し230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3000m/分にて引き取り、2.2dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が7.5g/m2 のウェブを形成した。
次にMFR900のポリプロピレンを常用のメルトブロー溶融紡糸装置に供給し、270℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmのポリプロピレン繊維からなる目付が2g/m2 のウェブを得た。
[Comparative Example 1]
1. MFR40 polypropylene resin (PP) is supplied to a conventional melt spinning apparatus, melted and mixed uniformly at 230 ° C., melt spun from a spinneret having a spinning hole having a circular cross section, and taken up at a speed of 3000 m / min. A 2 dtex polypropylene fiber was obtained. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 7.5 g / m 2 .
Next, MFR900 polypropylene is supplied to a conventional melt blow melt spinning apparatus, melted and mixed uniformly at 270 ° C., melt spun from a spinneret having a spinning hole with a circular cross section, and a basis weight made of 2.5 μm polypropylene fiber. A 2 g / m 2 web was obtained.
得られた2.5μmのポリプロピレンウェブを目付が7.5g/m2 のポリプロピレンからなるウェブで挟み、135℃に加熱したピンポイントエンボス(圧着面積7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して17g/m2 の不織布を作成した。得られた不織布の各物性を表2に示す。
得られた比較例1の積層不織布は、吸水速度は60秒以上と殆ど吸水せず、保水率は3.6%と非常に低いレベルであった。
The obtained 2.5 μm polypropylene web was sandwiched between polypropylene webs having a basis weight of 7.5 g / m 2 and heated at 135 ° C. between a pinpoint embossed (crimp area 7.1%) roll and a flat roll. A 17 g / m 2 nonwoven fabric was prepared by partial thermocompression bonding at 45 N / cm. Table 2 shows the physical properties of the obtained nonwoven fabric.
The laminated nonwoven fabric of Comparative Example 1 obtained had a water absorption rate of 60 seconds or more and hardly absorbed water, and the water retention rate was a very low level of 3.6%.
[比較例2]
MFR40のポリプロピレン樹脂(PP)を常用の溶融紡糸装置に供給し230℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度3000m/分にて引き取り、2.7dtexのポリプロピレン繊維を得た。得られたポリプロピレン繊維を開繊分散して目付が20g/m2 のウェブを形成し、135℃に加熱したピンポイントエンボス(圧着面積7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して20g/m2 の不織布を作成した。得られた不織布の各物性を表2に示す。
得られた比較例2の積層不織布は、吸水速度は60秒以上と殆ど吸水せず、保水率は3.4%と非常に低いレベルであった。
[Comparative Example 2]
1. MFR40 polypropylene resin (PP) is supplied to a conventional melt spinning apparatus, melted and mixed uniformly at 230 ° C., melt spun from a spinneret having a spinning hole having a circular cross section, and taken up at a speed of 3000 m / min. 7 dtex polypropylene fiber was obtained. The obtained polypropylene fiber was spread and dispersed to form a web having a basis weight of 20 g / m 2 , and a linear pressure of 45 N / cm between a pinpoint embossed (crimp area 7.1%) roll heated to 135 ° C. and a flat roll. Was subjected to partial thermocompression bonding to produce a 20 g / m 2 non-woven fabric. Table 2 shows the physical properties of the obtained nonwoven fabric.
The laminated nonwoven fabric of Comparative Example 2 obtained had a water absorption rate of 60 seconds or more and hardly absorbed water, and the water retention rate was a very low level of 3.4%.
[比較例3]
相対粘度が2.6のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が15g/m2 のウェブを形成した。
次に相対粘度が1.6のナイロン6を常用のメルトブロー溶融紡糸装置に供給し、290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmのナイロン6繊維からなる目付が10g/m2 のウェブを得た。
[Comparative Example 3]
Nylon 6 resin (N6) having a relative viscosity of 2.6 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The obtained nylon 6 fiber was spread and dispersed to form a web having a basis weight of 15 g / m 2 .
Next, nylon 6 having a relative viscosity of 1.6 is supplied to a conventional melt blow melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and 2.5 μm. A web made of nylon 6 fibers having a basis weight of 10 g / m 2 was obtained.
得られた2.5μmのナイロン6のウェブを目付が15g/m2 のナイロン6からなるウェブで挟み、175℃に加熱したピンポイントエンボス(圧着面積7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して40g/m2 の不織布を作成した。得られた不織布の各物性を表2に示す。
得られた比較例3の積層不織布は、吸水速度は40秒殆ど低い吸水性であり、保水率は12.8%と低いレベルであった。
The obtained 2.5 μm nylon 6 web is sandwiched between nylon 6 webs having a basis weight of 15 g / m 2 , and a wire is formed between a pinpoint embossed (crimp area 7.1%) roll heated to 175 ° C. and a flat roll. Partial thermocompression bonding was performed at a pressure of 45 N / cm to prepare a 40 g / m 2 nonwoven fabric. Table 2 shows the physical properties of the obtained nonwoven fabric.
The obtained laminated nonwoven fabric of Comparative Example 3 had a water absorption rate of almost low water absorption for 40 seconds, and a water retention rate as low as 12.8%.
[比較例4]
相対粘度が2.6のナイロン6樹脂(N6)を常用の溶融紡糸装置に供給し260℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4250m/分にて引き取り、2.0dtexのナイロン6繊維を得た。得られたナイロン6繊維を開繊分散して目付が40g/m2 のウェブを形成し、185℃に加熱したピンポイントエンボス(圧着面積7.1%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して40g/m2 の不織布を作成した。得られた不織布の各物性を表2に示す。
得られた比較例4の積層不織布は、吸水速度は45秒殆ど低い吸水性であり、保水率は12.3%と低いレベルであった。
[Comparative Example 4]
Nylon 6 resin (N6) having a relative viscosity of 2.6 is supplied to a conventional melt spinning apparatus, uniformly melt-mixed at 260 ° C., melt-spun from a spinneret having a spinning hole having a circular cross section, and a speed of 4250 m / min. To obtain 2.0 dtex of nylon 6 fiber. The resulting nylon 6 fiber was spread and dispersed to form a web having a basis weight of 40 g / m 2 , and a linear pressure of 45 N / b between a pinpoint embossed (crimp area 7.1%) roll and flat roll heated to 185 ° C. A 40 g / m 2 non-woven fabric was prepared by partial thermocompression bonding at cm. Table 2 shows the physical properties of the obtained nonwoven fabric.
The obtained laminated nonwoven fabric of Comparative Example 4 had a water absorption rate of almost 45 seconds and a low water absorption rate of 12.3%.
[比較例5]
固有粘度が0.77のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が30g/m2 のウェブを形成した。
次に固有粘度が0.49のポリエチレンテレフタレート樹脂(PET)を常用のメルトブロー溶融紡糸装置に供給し、310℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して2.5μmのポリエチレンテレフタレート繊維からなる目付が20g/m2 のウェブを得た。
[Comparative Example 5]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.77 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 30 g / m 2 .
Next, polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.49 is supplied to a conventional melt blow melt spinning apparatus, uniformly melted and mixed at 310 ° C., and melt spun from a spinneret having a spinning hole having a circular cross section. A web having a basis weight of 20 g / m 2 made of polyethylene terephthalate fibers of 2.5 μm was obtained.
得られた2.5μmのウェブを目付が30g/m2 のポリエチレンテレフタレート繊維からなるウェブで挟み230℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して80g/m2 の不織布を作成した。得られた不織布の各物性を表2に示す。
得られた比較例5の積層不織布は、吸水速度は60秒以上であり、殆ど吸水性を示さず、保水率は6.0%と低いレベルであった。
The obtained 2.5 μm web was sandwiched between polyethylene terephthalate fibers having a basis weight of 30 g / m 2 and heated to 230 ° C. between a rectangular pattern embossed (crimp area 11.4%) roll and a flat roll at a linear pressure of 45 N / A 80 g / m 2 nonwoven fabric was prepared by partial thermocompression bonding at cm. Table 2 shows the physical properties of the obtained nonwoven fabric.
The laminated nonwoven fabric of Comparative Example 5 obtained had a water absorption rate of 60 seconds or more, showed almost no water absorption, and had a low water retention rate of 6.0%.
[比較例6]
固有粘度が0.77のポリエチレンテレフタレート樹脂(PET)を常用の溶融紡糸装置に供給し290℃にて均一に溶融混合し、円形断面の紡糸孔を有する紡糸口金から溶融紡出して速度4500m/分にて引き取り、2.0dtexのポリエチレンテレフタレート繊維を得た。得られたポリエチレンテレフタレート繊維を開繊分散して目付が60g/m2 のウェブを形成し、220℃に加熱した長方形柄エンボス(圧着面積11.4%)ロールとフラットロール間で線圧45N/cmにて部分熱圧着して60g/m2 の不織布を作成した。得られた不織布の各物性を表2に示す。
得られた比較例6の積層不織布は、吸水速度は60秒以上であり、殆ど吸水性を示さず、保水率は5.8%と低いレベルであった。
[Comparative Example 6]
Polyethylene terephthalate resin (PET) having an intrinsic viscosity of 0.77 is supplied to a conventional melt spinning apparatus, uniformly melted and mixed at 290 ° C., melt-spun from a spinneret having a spinning hole with a circular cross section, and a speed of 4500 m / min. To obtain a polyethylene terephthalate fiber of 2.0 dtex. The obtained polyethylene terephthalate fiber was spread and dispersed to form a web having a basis weight of 60 g / m 2 , and a linear pressure 45 N / b between a rectangular pattern embossed (crimp area 11.4%) roll heated to 220 ° C. and a flat roll. A 60 g / m 2 non-woven fabric was prepared by partial thermocompression bonding at cm. Table 2 shows the physical properties of the obtained nonwoven fabric.
The laminated nonwoven fabric of Comparative Example 6 thus obtained had a water absorption rate of 60 seconds or more, hardly exhibited water absorption, and had a low water retention rate of 5.8%.
本発明の吸水性不織布積層体は、従来の吸水性材料が用いられている用途に広く使用可能であり、例えば、衣料部材、ディスポ衣料、靴部材などの衣料用途、保護衣、防護用品などの防護用途、手術着、マスク、ハップ剤基布などの医療用途、ルーフィング、タフト・カーペット基布、結露防止シートなどの建築用途、補強材、保護材、地中埋設管の補修材などの土木用途、自動車内装、自動車部品などの車両用途、救急用品、洗浄用品、おしぼりなどの衛生用途、カーペット、家具部材、壁紙などの家具・インテリア用途、ウェットワイパー、クリーニング材などのワイパー用途、空気フィルター、バグフィルター、エレクトレットフィルターなどのフィルター用途、布団、布団袋、枕カバーなどの寝装用途、べた掛けシート、防草シート、園芸プランターなどの農業・園芸用途、人工皮革用基布、合成皮革用基布、塩ビレザー用基布などの人工皮革類の基布用途、収納用品、食品等の包装資材、台所用品などの生活資材用途、電気材料、製品材料、機器部材などの工業資材用途などである。 The water-absorbing nonwoven fabric laminate of the present invention can be widely used in applications where conventional water-absorbing materials are used, such as apparel applications such as apparel members, disposable apparel, shoe members, protective clothing, protective articles, etc. Medical use such as protective use, surgical clothes, masks, haptic base fabrics, roofing, tuft / carpet base fabrics, anti-condensation sheets, etc., civil engineering uses such as reinforcing materials, protective materials, repair materials for underground pipes , Automotive interiors, automotive parts and other vehicle applications, emergency supplies, cleaning products, hand towels and other hygiene applications, carpets, furniture parts, wallpaper and other furniture / interior applications, wet wipers, cleaning materials and other wiper applications, air filters, bugs Filter applications such as filters and electret filters, bedding applications such as futons, futon bags, pillow covers, solid sheets, grass protection sheets Agricultural and horticultural applications such as horticultural planters, artificial leather base fabrics, synthetic leather base fabrics, artificial leather base fabrics such as PVC leather base fabrics, storage materials, packaging materials such as food, kitchen utensils, etc. It is used for industrial materials such as materials, electrical materials, product materials, and equipment members.
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009276034A (en) * | 2008-05-19 | 2009-11-26 | Asahi Kasei Fibers Corp | Fiber structure for vaporization filter |
| JP2012057290A (en) * | 2009-02-06 | 2012-03-22 | Nike Internatl Ltd | Composite element and manufacturing method thereof |
| US8906275B2 (en) | 2012-05-29 | 2014-12-09 | Nike, Inc. | Textured elements incorporating non-woven textile materials and methods for manufacturing the textured elements |
| WO2015194563A1 (en) * | 2014-06-17 | 2015-12-23 | 株式会社クラレ | Water absorbent laminate and method for producing same |
| US9682512B2 (en) | 2009-02-06 | 2017-06-20 | Nike, Inc. | Methods of joining textiles and other elements incorporating a thermoplastic polymer material |
| JP2020016000A (en) * | 2018-07-26 | 2020-01-30 | 東レ株式会社 | Laminated non-woven fabric |
| JPWO2021010178A1 (en) * | 2019-07-16 | 2021-01-21 | ||
| WO2023000643A1 (en) * | 2021-07-19 | 2023-01-26 | 厦门延江新材料股份有限公司 | Super-soft composite wiping non-woven fabric and manufacturing method therefor |
| US11779071B2 (en) | 2012-04-03 | 2023-10-10 | Nike, Inc. | Apparel and other products incorporating a thermoplastic polymer material |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05321115A (en) * | 1992-05-18 | 1993-12-07 | Toray Ind Inc | Laminated nonwoven fabric and its production |
| JP2003166173A (en) * | 2001-09-20 | 2003-06-13 | Mitsui Chemicals Inc | Fiber sheet and protective working clothes |
| JP2003201670A (en) * | 2001-12-28 | 2003-07-18 | Chisso Corp | Hydrophilic long-fiber nonwoven fabric, composite nonwoven fabric, and absorbent article using them |
| JP2005036321A (en) * | 2003-07-15 | 2005-02-10 | Chisso Corp | Thermal adhesive composite fiber, nonwoven fabric and product using the same |
-
2005
- 2005-04-15 JP JP2005117854A patent/JP4854214B2/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05321115A (en) * | 1992-05-18 | 1993-12-07 | Toray Ind Inc | Laminated nonwoven fabric and its production |
| JP2003166173A (en) * | 2001-09-20 | 2003-06-13 | Mitsui Chemicals Inc | Fiber sheet and protective working clothes |
| JP2003201670A (en) * | 2001-12-28 | 2003-07-18 | Chisso Corp | Hydrophilic long-fiber nonwoven fabric, composite nonwoven fabric, and absorbent article using them |
| JP2005036321A (en) * | 2003-07-15 | 2005-02-10 | Chisso Corp | Thermal adhesive composite fiber, nonwoven fabric and product using the same |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| US10138582B2 (en) | 2009-02-06 | 2018-11-27 | Nike, Inc. | Thermoplastic non-woven textile elements |
| US12404615B2 (en) | 2009-02-06 | 2025-09-02 | Nike, Inc. | Thermoplastic non-woven textile elements |
| US9227363B2 (en) | 2009-02-06 | 2016-01-05 | Nike, Inc. | Thermoplastic non-woven textile elements |
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| US9682512B2 (en) | 2009-02-06 | 2017-06-20 | Nike, Inc. | Methods of joining textiles and other elements incorporating a thermoplastic polymer material |
| US9732454B2 (en) | 2009-02-06 | 2017-08-15 | Nike, Inc. | Textured elements incorporating non-woven textile materials and methods for manufacturing the textured elements |
| US10982363B2 (en) | 2009-02-06 | 2021-04-20 | Nike, Inc. | Thermoplastic non-woven textile elements |
| JP2012057290A (en) * | 2009-02-06 | 2012-03-22 | Nike Internatl Ltd | Composite element and manufacturing method thereof |
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| US11779071B2 (en) | 2012-04-03 | 2023-10-10 | Nike, Inc. | Apparel and other products incorporating a thermoplastic polymer material |
| US8906275B2 (en) | 2012-05-29 | 2014-12-09 | Nike, Inc. | Textured elements incorporating non-woven textile materials and methods for manufacturing the textured elements |
| JPWO2015194563A1 (en) * | 2014-06-17 | 2017-04-20 | 株式会社クラレ | Water-absorbent laminate and method for producing the same |
| WO2015194563A1 (en) * | 2014-06-17 | 2015-12-23 | 株式会社クラレ | Water absorbent laminate and method for producing same |
| JP2020016000A (en) * | 2018-07-26 | 2020-01-30 | 東レ株式会社 | Laminated non-woven fabric |
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| CN114126742A (en) * | 2019-07-16 | 2022-03-01 | 可乐丽可乐富丽世股份有限公司 | Fiber structure and method for producing same |
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