JPWO2006095623A1 - Nonwoven fabric for cleaning - Google Patents

Nonwoven fabric for cleaning Download PDF

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JPWO2006095623A1
JPWO2006095623A1 JP2007507066A JP2007507066A JPWO2006095623A1 JP WO2006095623 A1 JPWO2006095623 A1 JP WO2006095623A1 JP 2007507066 A JP2007507066 A JP 2007507066A JP 2007507066 A JP2007507066 A JP 2007507066A JP WO2006095623 A1 JPWO2006095623 A1 JP WO2006095623A1
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fiber
nonwoven fabric
cleaning
mass
pva
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友浩 早川
友浩 早川
凪 比佐志
比佐志 凪
豊浦 仁
仁 豊浦
林 英男
英男 林
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Kuraray Co Ltd
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Kuraray Co Ltd
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    • AHUMAN NECESSITIES
    • A47FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47LDOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
    • A47L13/00Implements for cleaning floors, carpets, furniture, walls, or wall coverings
    • A47L13/10Scrubbing; Scouring; Cleaning; Polishing
    • A47L13/16Cloths; Pads; Sponges
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4391Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres
    • D04H1/43912Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres fibres with noncircular cross-sections
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/253Formation of filaments, threads, or the like with a non-circular cross section; Spinnerette packs therefor
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/14Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated alcohols, e.g. polyvinyl alcohol, or of their acetals or ketals
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4282Addition polymers
    • D04H1/4309Polyvinyl alcohol
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4391Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres
    • D04H1/43918Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece characterised by the shape of the fibres nonlinear fibres, e.g. crimped or coiled fibres

Abstract

【課題】洗剤や潤滑剤、研磨剤、漂白剤等を必要とせず、食器や目地にキズを生じずに茶渋やカビ等を除去することができる清掃用不織布を提供する。【解決手段】繊維断面が扁平形状しており、その断面において扁平度が6〜30であり、かつ繊維の外周長手方向に溝が形成してなるポリビニルアルコール系繊維が30質量%以上含有されてなる不織布で構成される清掃用不織布。Disclosed is a non-woven fabric for cleaning that does not require detergents, lubricants, abrasives, bleaching agents, etc., and can remove tea astringency and mold without causing scratches on tableware and joints. SOLUTION: The cross section of the fiber has a flat shape, the flatness is 6-30 in the cross section, and 30% by mass or more of polyvinyl alcohol fiber formed by forming a groove in the longitudinal direction of the outer periphery of the fiber is contained. A nonwoven fabric for cleaning composed of a nonwoven fabric.

Description

本発明はわずかな油汚れから、茶渋、水垢あるいはピッチ系の頑固にこびりついた汚れまで、洗剤を用いなくても容易に除去することが可能な清掃用不織布に関する。  The present invention relates to a non-woven fabric for cleaning that can be easily removed without using a detergent, from slight oil stains to stubbornly sticky stains such as tea astringents, scales or pitches.

従来より各家庭では、茶碗にこびりついた茶渋や風呂場のタイルの目地等に生じたカビを除去するために、次亜塩素酸ナトリウムを主成分とする漂白剤を、希釈した溶液に浸漬したり霧や泡状にして吹き付けて使用されている。しかしながら次亜塩素酸ナトリウムを使用した溶液はアルカリ性が強いため皮膚を荒らしたり、特に酸性の洗浄剤と混用すると大量の塩素ガスが急激に発生して目や喉の粘膜を刺激し、人体に影響を及ぼしたり、安全性に欠けるという問題点を有していた。  Conventionally, in each household, a bleaching agent containing sodium hypochlorite as a main component has been immersed in a diluted solution in order to remove mold generated on tea pots stuck to teacups or tile joints in bathrooms. It is used in the form of mist or foam. However, a solution using sodium hypochlorite has strong alkalinity and causes rough skin, especially when mixed with an acidic cleaning agent, a large amount of chlorine gas is generated suddenly, irritating the mucous membrane of the eyes and throat, affecting the human body. And has a problem of lack of safety.

また、鍋や釜にこびりついた焦げ等を擦り落とすために、亀の子タワシ、スチールウール、あるいはナイロン不織布に硬度の大きい砥粒を強固に固着したナイロンタワシや、同様のナイロンタワシを片面に接着したスポンジ等が使用されている。しかしながら、亀の子タワシやスチールウール、ナイロンタワシ等は表面が粗くしかも硬いため、ガラス製や陶磁器製、プラスチック製等の食器やタイルの目地等を傷めやすく、したがってこれらには適用できないという問題点を有していた。  In addition, in order to scrub off burns stuck to pots and kettles, glue a nylon scrub on a single side or a nylon scrub with strong hardness on a turtle scallop, steel wool, or nylon nonwoven fabric. Sponge etc. are used. However, turtle scallops, steel wool, nylon scourers, etc. have a rough and hard surface, which easily damages tableware and tile joints made of glass, ceramics, plastics, etc., and therefore cannot be applied to these. Had.

これらの問題点を改良するために、繊維表面積の大きい扁平形状の繊維を清掃用不織布に用いることで清掃時の掻き取り性能が良好になることが記載されている(例えば、特許文献1参照。)。このような扁平繊維使いの清掃用不織布は従来の扁平繊維を使用しない不織布に比べて性能は向上しているが、落ちにくい汚れに対する除去性能は繊維断面端部のエッジ部分の減少により効果がみられなかった。この繊維断面端部のエッジによる除去効果を改善させるために砥粒を繊維表面に付与した清掃用不織布が提案されている(例えば、特許文献2〜4参照。)。しかしながら、これら清掃用不織布で汚れを除去しようとする場合、清掃面と接触する部分が局所的になるため、汚れの除去に要する拭き取り回数が多くなったり、あるいは硬質の砥粒を使用しているためキズが付き易く、食器や水周りに適用できないという問題点を有していた。  In order to improve these problems, it is described that the scraping performance at the time of cleaning is improved by using flat fibers having a large fiber surface area for the nonwoven fabric for cleaning (see, for example, Patent Document 1). ). Such cleaning nonwoven fabrics using flat fibers have improved performance compared to conventional nonwoven fabrics that do not use flat fibers, but the removal performance against dirt that is difficult to remove is more effective by reducing the edge of the fiber cross section. I couldn't. In order to improve the removal effect by the edge of this fiber cross-section edge part, the nonwoven fabric for cleaning which provided the abrasive grain to the fiber surface is proposed (for example, refer patent documents 2-4). However, when removing dirt with these cleaning nonwoven fabrics, the portion that comes into contact with the cleaning surface becomes local, so the number of wiping required to remove the dirt increases, or hard abrasive grains are used. Therefore, there was a problem that it was easily scratched and could not be applied to tableware or water.

これらに対し、繊維自体ではなく不織布の片面又は両面を接着剤で砥粒を固着させた清掃用不織布が提案されている(例えば、特許文献5〜12参照。)。しかしながら、これらの清掃用不織布は、砥粒を固着させた部分しか清掃能力がなく、清掃時に接着剤層が磨耗するのと同時に砥粒が剥がれるので清掃能力の持続性が低いという問題点を有していた。  On the other hand, the nonwoven fabric for cleaning which fixed the abrasive grain with the adhesive agent on the single side | surface or both surfaces of the nonwoven fabric instead of fiber itself is proposed (for example, refer patent documents 5-12). However, these non-woven fabrics for cleaning have a problem that only the portion to which the abrasive grains are fixed has a cleaning ability, and the abrasive grains are peeled off at the same time as the adhesive layer is worn during cleaning, so that the sustainability of the cleaning ability is low. Was.

また、砥粒を使用せず不織布を構成する繊維に多孔質の樹脂層を形成した清掃用不織布が提案されていたり(例えば、特許文献13〜15参照。)、さらには、熱硬化性樹脂を不織布に付着させる方法が提案されている(例えば、特許文献16参照。)。しかしながら、これらの清掃用不織布は別途砥粒を含む研磨材を用意して同時に使用しないと茶渋等に対する清掃能力に劣るという問題点があった。  Moreover, the nonwoven fabric for cleaning which formed the porous resin layer in the fiber which comprises a nonwoven fabric without using an abrasive grain is proposed (for example, refer patent documents 13-15), Furthermore, thermosetting resin is used. A method of adhering to a nonwoven fabric has been proposed (see, for example, Patent Document 16). However, these non-woven fabrics for cleaning have a problem that the cleaning ability for tea astringency is inferior unless an abrasive containing abrasive grains is prepared and used simultaneously.

特開昭55−58147号公報JP-A-55-58147 特開平5−220670号公報JP-A-5-220670 特開平6−155310号公報JP-A-6-155310 特開平6−155311号公報Japanese Patent Laid-Open No. 6-155311 特開平5−28477号公報Japanese Patent Laid-Open No. 5-28477 特開平5−57622号公報JP-A-5-57622 特開平5−253850号公報JP-A-5-253850 特開平5−285854号公報Japanese Patent Laid-Open No. 5-285854 特開平6−238570号公報JP-A-6-238570 特開平7−100769号公報Japanese Patent Laid-Open No. 7-100769 特開平8−300252号公報JP-A-8-300252 特開平9−22886号公報Japanese Patent Laid-Open No. 9-22886 特開平6−17374号公報JP-A-6-17374 特開平7−108464号公報JP-A-7-108464 特開平7−108465号公報JP-A-7-108465 特表2000−508000号公報Special Table 2000-508000

本発明の目的は、洗剤や潤滑剤、研磨剤、漂白剤等を必要とせず、食器や目地にキズを付けることなく茶渋やカビ等を除去することができる清掃用不織布を提供することである。  An object of the present invention is to provide a non-woven fabric for cleaning that does not require detergents, lubricants, abrasives, bleaching agents, etc., and can remove tea astringency, mold, etc. without scratching tableware or joints. .

本発明者等は、上記した清掃用不織布を得るべく鋭意検討を重ねた結果、水及び油との馴染みが良好であり、さらに図1に示すような、繊維表面に溝を形成する扁平形状のポリビニルアルコール(以下、PVAと略記する)系繊維を使用し、さらに好ましくは該繊維からなる不織布に高分子系樹脂状物を付着させるか、あるいは熱融着繊維からなるバインダー繊維を混綿することによって、清掃面への接地面積増加とエッジ増加により上記目的が達成可能な清掃用不織布得られることを見出した。
すなわち本発明は、繊維断面が扁平形状しており、その断面において扁平度が6〜30であり、かつ繊維の外周長手方向に溝が形成してなるPVA系繊維が30質量%以上含有されてなる不織布で構成される清掃用不織布であり、好ましくはPVA系繊維が、繊維の外周長手方向に深さ0.1〜2.0μmの溝が10μm間隔以内に1個以上有する繊維である上記の清掃用不織布であり、より好ましくはPVA系繊維の単繊維繊度が0.5〜5dtex、繊維長が5〜80mmである上記の清掃用不織布であり、さらに好ましくはPVA系繊維が平均粒子径0.01〜30μmの層状化合物を0.5〜30質量%含有されてなる繊維である上記の清掃用不織布である。
As a result of intensive studies to obtain the above-described nonwoven fabric for cleaning, the present inventors have a good familiarity with water and oil, and further have a flat shape that forms grooves on the fiber surface as shown in FIG. By using a polyvinyl alcohol (hereinafter abbreviated as PVA) fiber, more preferably by attaching a polymer resin to a nonwoven fabric made of the fiber, or by blending a binder fiber made of a heat fusion fiber The present inventors have found that a nonwoven fabric for cleaning that can achieve the above-described object can be obtained by increasing the contact area to the cleaning surface and increasing the edge.
That is, in the present invention, the fiber cross section has a flat shape, the flatness is 6 to 30 in the cross section, and 30% by mass or more of PVA fiber formed by forming a groove in the outer peripheral longitudinal direction of the fiber is contained. The nonwoven fabric for cleaning composed of the nonwoven fabric, preferably the PVA fiber is a fiber having one or more grooves having a depth of 0.1 to 2.0 μm within 10 μm intervals in the longitudinal direction of the outer periphery of the fiber. A non-woven fabric for cleaning, more preferably the above-mentioned non-woven fabric for cleaning having a single fiber fineness of PVA fibers of 0.5 to 5 dtex and a fiber length of 5 to 80 mm, more preferably PVA fibers having an average particle size of 0. It is said nonwoven fabric for cleaning which is a fiber containing 0.5-30 mass% of layered compounds of 0.01-30 micrometers.

また本発明は、好ましくは不織布のいずれかの方向での3%伸長時の引張強力が1.0kg/25mm以上である上記の清掃用不織布であり、より好ましくは熱融着繊維からなるバインダー繊維を10質量%以上混綿してなる上記の清掃用不織布であり、さらに好ましくは高分子系樹脂状物を不織布重量に対して5〜200質量%付与してなる上記の清掃用不織布であり、そして不織布に付与してなる上記高分子系樹脂状物が熱硬化性樹脂からなる清掃用不織布である。  Further, the present invention is preferably the above-mentioned non-woven fabric for cleaning having a tensile strength at 3% elongation in any direction of the non-woven fabric of 1.0 kg / 25 mm or more, more preferably a binder fiber comprising a heat-sealing fiber. 10% by mass or more of the above-mentioned non-woven fabric for cleaning, more preferably, the above-mentioned non-woven fabric for cleaning formed by adding 5 to 200% by mass of the polymer resinous material to the non-woven fabric weight, and The said high molecular resin-like material provided to a nonwoven fabric is a nonwoven fabric for cleaning which consists of thermosetting resins.

本発明によれば、清掃性に優れると共に拭き取り対象物にキズが付かない、優れた清掃能力を有する清掃用不織布を提供することが可能であり、特にわずかな油汚れから茶渋、水垢あるいはピッチ系の頑固にこびりついた汚れまで洗剤を用いなくても容易に除去することができる。  ADVANTAGE OF THE INVENTION According to this invention, it is possible to provide the nonwoven fabric for cleaning which is excellent in cleaning property, and does not damage the object to be wiped and has excellent cleaning ability. Even stubbornly sticky dirt can be easily removed without using a detergent.

以下に本発明について具体的に説明する。まず本発明で使用されるPVA系繊維の繊維断面は扁平形状である必要がある。具体的には繊維断面の長辺と短辺の長さの比で表される扁平度が6〜30であることが必要であり、好ましくは10〜25である。PVA系繊維の断面形状が繭型断面や丸型断面、あるいは扁平度が6未満である場合、清掃面との接地面積が小さくなり、本発明の目的とする清掃性能が得られない。逆に扁平度が30を超える場合は紡糸時に仮接着した繊維同士の界面が剥離しにくくなり、該繊維から不織布を製造した場合、貝柱状の塊がシート内に多数発生し、また構成繊維本数の低減化を招き、拭取り性能が低下してしまう。  The present invention will be specifically described below. First, the fiber cross section of the PVA fiber used in the present invention needs to be flat. Specifically, the flatness expressed by the ratio of the long side to the short side length of the fiber cross section is required to be 6 to 30, and preferably 10 to 25. When the cross-sectional shape of the PVA fiber is a saddle-shaped cross-section, a round cross-section, or a flatness of less than 6, the contact area with the cleaning surface becomes small, and the cleaning performance intended by the present invention cannot be obtained. Conversely, when the flatness exceeds 30, the interface between the fibers temporarily bonded during spinning becomes difficult to peel off, and when a nonwoven fabric is produced from the fibers, a large number of shell-like lumps are generated in the sheet, and the number of constituent fibers This leads to a reduction in the wiping performance.

また本発明に用いられるPVA系繊維は、上記した扁平度を有するとともに、繊維の表面には繊維の外周長手方向に溝が形成してなることが重要であり、具体的には繊維の外周長手方向に深さ0.1〜2.0μmの溝が10μm間隔以内に1個以上存在していることが好ましい。この溝は繊維製造時の凝固速度制御により形成させることができ、汚れの掻き取り時にエッジ効果を発現し汚れ除去性能を向上させることができる。この溝が10μm間隔以内に1個未満となる場合、十分な掻き取り性能を得ることができない場合がある。さらに汚れ除去性能を向上させるためには10μm間隔以内に3個以上10個以下存在していることが好ましい。溝の深さについては0.1μm未満であると、後述する高分子樹脂状物あるいは清掃時の汚れにより埋没してしまうことがあり、一方、2.0μmを超えると溝部分によって繊維が裂け易くなってしまい、不織布をシート化する時の地合形成性を阻害してしまうことがある。より好ましくは0.3〜1.5μm、さらに好ましくは0.5〜1.0μmである。  In addition, the PVA fiber used in the present invention has the above-described flatness, and it is important that a groove is formed on the surface of the fiber in the longitudinal direction of the outer periphery of the fiber. It is preferable that at least one groove having a depth of 0.1 to 2.0 μm exists in the direction within an interval of 10 μm. This groove can be formed by controlling the solidification rate at the time of fiber production, and can exhibit an edge effect when the dirt is scraped to improve the dirt removing performance. If the number of grooves is less than 1 within 10 μm, sufficient scraping performance may not be obtained. Further, in order to improve the dirt removing performance, it is preferable that 3 or more and 10 or less exist within an interval of 10 μm. If the depth of the groove is less than 0.1 μm, it may be buried due to a polymer resinous material to be described later or dirt during cleaning. On the other hand, if the depth exceeds 2.0 μm, the fiber easily breaks by the groove portion. In other words, the formation of the nonwoven fabric may be hindered. More preferably, it is 0.3-1.5 micrometers, More preferably, it is 0.5-1.0 micrometer.

図1に本発明のPVA系繊維の繊維断面写真を、また図2に従来より製造されているPVA系繊維の繊維断面写真を示す。図2の従来より製造されているPVA系繊維の断面形状は繭型といわれるのに対し、図1の本発明のPVA系繊維の断面は短辺の厚みが非常に薄い扁平形状を有し、かつ繊維表面には、繊維の長手方向に連続する溝が存在することがわかる。  FIG. 1 shows a fiber cross-sectional photograph of the PVA fiber of the present invention, and FIG. 2 shows a fiber cross-sectional photograph of a PVA fiber manufactured conventionally. The cross-sectional shape of the PVA-based fiber manufactured conventionally in FIG. 2 is called a saddle shape, whereas the cross-sectional shape of the PVA-based fiber of the present invention in FIG. 1 has a flat shape with a very short short side, And it turns out that the groove | channel which continues in the longitudinal direction of a fiber exists in the fiber surface.

本発明のPVA系繊維の製造において使用されるPVA系ポリマーは特に制限はなく、例えばカルボン酸基、スルホン酸基、エチレン基、シラン基、シラノール基、アミン基、アンモニウム基等のいずれか一つまたは二つ以上共重合していても構わない。またPVAのケン化度についても特に制限はなく、ケン化度85〜99.9モル%、好ましくは96〜99.9モル%のものが用いられる。  The PVA polymer used in the production of the PVA fiber of the present invention is not particularly limited, and for example, any one of a carboxylic acid group, a sulfonic acid group, an ethylene group, a silane group, a silanol group, an amine group, an ammonium group, and the like. Alternatively, two or more may be copolymerized. The saponification degree of PVA is not particularly limited, and those having a saponification degree of 85 to 99.9 mol%, preferably 96 to 99.9 mol% are used.

本発明のPVA系繊維の製造方法は特に制限はなく、乾式紡糸、湿式紡糸、乾湿式紡糸などが挙げられるが、生産性および品質の面から湿式紡糸が好適に採用される。
中でも湿式紡糸の方法には大きく分けて二つの方法が挙げられる。一つはPVA系ポリマーを水に溶解させて紡糸原液とした後、ノズル孔より凝固能を有する塩類の水溶液中に吐出させて繊維化する水系湿式紡糸法、もう一つはPVA系ポリマーを有機溶媒中に溶解させて紡糸原液とした後、ノズル孔より固化能を有する有機溶剤中に吐出させて繊維化する有機溶剤系湿式紡糸法であり、これらの何れの方法を用いることができる。
The method for producing the PVA fiber of the present invention is not particularly limited, and examples thereof include dry spinning, wet spinning, dry and wet spinning, and wet spinning is preferably employed from the viewpoint of productivity and quality.
Among them, the wet spinning method is roughly divided into two methods. One is a water-based wet spinning method in which a PVA polymer is dissolved in water to form a spinning stock solution, and then discharged into an aqueous solution of a salt having a coagulation ability through a nozzle hole to form a fiber. The other is a PVA polymer organically. This is an organic solvent-based wet spinning method in which a spinning solution is prepared by dissolving in a solvent, and then discharged into an organic solvent having a solidifying ability through a nozzle hole to form a fiber. Any of these methods can be used.

上記した紡糸法のうち、水系湿式紡糸法について以下説明する。
具体的には、まずPVA系ポリマーを水に溶解させてなる紡糸原液を調製する。このとき用いるPVA系ポリマーの重合度に特に制限はないが、一般的には重合度500〜4000であることが好ましく、より好ましくは1000〜2500の範囲のものが用いられる。重合度が500未満では分子鎖のからみが小さく、延伸工程で十分な延伸性が得られないので、結果として繊維強度や耐水性等の物性が低下してしまう。また重合度が4000を越えると、原液の粘度が著しく上昇するため、原液中のPVA系ポリマーの濃度を低下させる必要があるため、生産性が低下してしまう。紡糸時の原液濃度についても10〜20質量%の濃度が好ましい。原液濃度が10質量%未満であるとPVA系樹脂の吐出量が低下し生産性が低下してしまう。逆に20質量%を超えると脱水による体積収縮が小さくなり、繊維表面の溝が形成されにくくなる。
Of the above spinning methods, the water-based wet spinning method will be described below.
Specifically, first, a spinning dope is prepared by dissolving a PVA polymer in water. Although there is no restriction | limiting in particular in the polymerization degree of the PVA type polymer used at this time, Generally it is preferable that it is a polymerization degree 500-4000, More preferably, the thing of the range of 1000-2500 is used. If the degree of polymerization is less than 500, the entanglement of the molecular chain is small, and sufficient stretchability cannot be obtained in the stretching step. As a result, physical properties such as fiber strength and water resistance are lowered. On the other hand, when the degree of polymerization exceeds 4000, the viscosity of the stock solution is remarkably increased, so that the concentration of the PVA polymer in the stock solution needs to be lowered. The concentration of the stock solution at the time of spinning is preferably 10 to 20% by mass. When the concentration of the stock solution is less than 10% by mass, the discharge amount of the PVA-based resin is lowered and the productivity is lowered. On the other hand, if it exceeds 20% by mass, the volume shrinkage due to dehydration becomes small, and it becomes difficult to form grooves on the fiber surface.

本発明のPVA系繊維は、上記したPVA系ポリマーとともに、層状化合物を添加することにより凝固時の体積収縮が大きくなり繊維表面に形成された溝の高低差がより大きな繊維が得られるので好ましい。層状化合物としては、例えばスメクタイト、モンモリロナイト、雲母等が挙げられる。またこれらは、天然物あるいは合成物のいずれであっても構わない。ただし、繊維の紡糸原液に添加するためには、その平均粒子径は0.01〜30μmの範囲であることが好ましい。平均粒子径が30μmを越えると紡糸ノズルや濾過フィルターが目詰まりを起こし、紡糸性が悪化する。一方、平均粒子径が0.01μmよりも小さい場合、層状化合物どうしが凝集してしまい、結果として二次粒子は数十μm以上となり、紡糸ノズルや濾過フィルターが目詰まりを起こし、紡糸性が悪化する。より好ましくは平均粒子径0.1〜10μmである。  The PVA fiber of the present invention is preferable because, by adding a layered compound together with the above-described PVA polymer, a volume shrinkage at the time of coagulation is increased and a fiber having a larger difference in height of grooves formed on the fiber surface is obtained. Examples of the layered compound include smectite, montmorillonite, mica and the like. These may be natural products or synthetic products. However, in order to add to the fiber spinning dope, the average particle size is preferably in the range of 0.01 to 30 μm. When the average particle diameter exceeds 30 μm, the spinning nozzle and the filter are clogged, and the spinnability is deteriorated. On the other hand, when the average particle diameter is smaller than 0.01 μm, the layered compounds are aggregated. As a result, the secondary particles become several tens of μm or more, and the spinning nozzle and the filter are clogged, and the spinning property is deteriorated. To do. More preferably, the average particle size is 0.1 to 10 μm.

また層状化合物の繊維への添加量は、繊維に対して0.5〜30質量%添加することが好ましい。添加量が0.5質量%より少ない場合は繊維表面に形成された溝の高低差にあまり変化が見られない。逆に添加量が30質量%を越えると紡糸性が不安定となるばかりか、得られた繊維の物性も著しく低下してしまう。より好ましくは1〜10質量%である。  Moreover, it is preferable that the addition amount to the fiber of a layered compound is added 0.5-30 mass% with respect to a fiber. When the addition amount is less than 0.5% by mass, there is not much change in the height difference of the grooves formed on the fiber surface. On the contrary, if the addition amount exceeds 30% by mass, not only the spinnability becomes unstable, but also the physical properties of the obtained fiber are remarkably lowered. More preferably, it is 1-10 mass%.

本発明のPVA系繊維を製造する際に、紡糸で用いるノズル単孔の形状はスリット形状とすることが好ましい。具体的には長辺180〜1000μm、短辺30〜80μmの長方形型、あるいはその長方形の長端を半円状にしたもの、あるいは長端を円形処理した、いわゆる「ドックボーン」形状のものが用いられる。ただし、得られる繊維の断面形状は必ずしもノズル形状と一致しないため、ノズル単孔の長辺/短辺の比は5〜50の範囲が好適であり、この範囲とすることで本発明の目的とする扁平断面形状のPVA系繊維を得ることができる。  When the PVA fiber of the present invention is produced, the shape of the nozzle single hole used for spinning is preferably a slit shape. Specifically, a rectangular shape having a long side of 180 to 1000 μm and a short side of 30 to 80 μm, a long end of the rectangle made into a semicircle, or a so-called “dockbone” shape in which the long end is circularly processed. Used. However, since the cross-sectional shape of the obtained fiber does not necessarily match the nozzle shape, the ratio of the long side / short side of the nozzle single hole is preferably in the range of 5 to 50. A PVA fiber having a flat cross-sectional shape can be obtained.

上記した形状のノズルを用いて紡糸原液を通過させ、飽和硫酸ナトリウム水溶液中に吐出させ、第一ローラーで巻取り、次いで水を含んだままの状態で3〜4倍の湿延伸を行う。湿延伸後130℃の熱風乾燥機中で定長乾燥を行い、引き続いて230℃の熱風炉中でさらに2〜3倍の乾熱延伸を行うことにより本発明の繊維を得ることができる。なお、本発明のPVA系繊維はこのまま使用することは勿論のこと、引き続いてホルムアルデヒドによるホルマール化処理を施して耐水性を付与してもかまわない。  The spinning solution is passed through the nozzle having the shape described above, discharged into a saturated aqueous solution of sodium sulfate, wound up with a first roller, and then wet stretched 3-4 times while still containing water. The fiber of the present invention can be obtained by performing constant length drying in a hot air dryer at 130 ° C. after the wet stretching, and further performing dry heat stretching 2 to 3 times in a hot air oven at 230 ° C. The PVA fiber of the present invention can be used as it is, and subsequently subjected to a formalization treatment with formaldehyde to impart water resistance.

本発明のPVA系繊維は短繊維、長繊維の何れも使用可能である。短繊維が用いられる場合、繊維長は不織布の製造のしやすさおよび使用中における繊維の脱落を防止する点から、5〜80mm、好ましくは10〜60mmである。繊維長が80mmを超えると繊維が絡まってしまいカードでの地合形成ができなくなる。逆に5mm未満であると繊維の脱落が激しくなる。  Either short fibers or long fibers can be used for the PVA fibers of the present invention. When short fibers are used, the fiber length is 5 to 80 mm, preferably 10 to 60 mm, from the viewpoint of ease of manufacturing the nonwoven fabric and preventing the fibers from falling off during use. If the fiber length exceeds 80 mm, the fibers become entangled and formation with a card cannot be performed. On the other hand, if the thickness is less than 5 mm, the fibers will fall off drastically.

本発明のPVA系繊維の繊度は0.5〜5dtexであることが好ましい。0.5dtex未満であるとアスペクト比の低下により繊維が絡まりやすく、シート化時に地合の乱れたシートになってしまう。一方、繊度が5dtexを越えると不織布を構成する繊維本数は低減し、表面の粗い不織布となってしまい、本発明の目的とする清掃時の掻き取り効果を得ることができない。より好ましくは1〜4dtexである。なお、繊維の繊度はノズル径や延伸倍率により適宜調整すればよい。  The fineness of the PVA fiber of the present invention is preferably 0.5 to 5 dtex. If it is less than 0.5 dtex, the fibers are likely to be entangled due to a decrease in aspect ratio, resulting in a sheet with a disordered formation when formed into a sheet. On the other hand, if the fineness exceeds 5 dtex, the number of fibers constituting the non-woven fabric is reduced, resulting in a non-woven fabric with a rough surface, and the scraping effect during cleaning, which is the object of the present invention, cannot be obtained. More preferably, it is 1-4 dtex. The fineness of the fiber may be adjusted as appropriate depending on the nozzle diameter and the draw ratio.

このようにして得られた繊維は、以下の方法により乾式不織布を製造することができる。
例えば、まず本発明のPVA系繊維を機械捲縮し、繊維長を51mmにカットし、カーディングしてウェッブを作製する。ウェッブ作製の際、使用する繊維は当該繊維単独でもよいが、レーヨン、ポリノジック、溶剤紡糸セルロース繊維、アセテート、ポリエステル、ナイロン、アクリル、ポリエチレン、ポリプロピレン、ポリ乳酸系繊維、綿などの1種あるいは2種以上を混綿してもかまわない。本発明のPVA系繊維の配合率は30質量%以上であることが必要であり、好ましくは50質量%以上、より好ましくは70質量%以上100質量%以下である。配合率が30質量%未満であると、拭取り面へ接地するPVA系繊維の絶対量が少なく、掻き取り効果が不十分に得られない。こうして得られたウェッブは30kg/cm以上の高圧水流をあてること、もしくは250本/cm以上の密度でニードルパンチすることにより乾式不織布を得ることができる。
The fiber thus obtained can produce a dry nonwoven fabric by the following method.
For example, first, the PVA fiber of the present invention is mechanically crimped, cut to a fiber length of 51 mm, and carded to produce a web. When producing a web, the fiber used may be the fiber alone, but one or two of rayon, polynosic, solvent-spun cellulose fiber, acetate, polyester, nylon, acrylic, polyethylene, polypropylene, polylactic acid fiber, cotton, etc. The above may be blended. The blending ratio of the PVA fiber of the present invention needs to be 30% by mass or more, preferably 50% by mass or more, more preferably 70% by mass or more and 100% by mass or less. When the blending ratio is less than 30% by mass, the absolute amount of the PVA fiber that contacts the wiping surface is small, and the scraping effect cannot be obtained insufficiently. A dry nonwoven fabric can be obtained by applying a high-pressure water flow of 30 kg / cm 2 or more to the web thus obtained, or by needle punching at a density of 250 pieces / cm 2 or more.

一方、当該繊維を繊維長10mmにカットし、バインダー繊維とともに湿式抄造することにより湿式不織布を得ることができる。このとき、上記の乾式不織布の製造の場合と同様、他種の繊維が70質量%未満となるように混抄してもかまわない。本発明の繊維を少なくとも一部として含むスラリーを抄造して得られた原紙に、30kg/cm以上の高圧水流をあてることにより湿式不織布を得ることができる。On the other hand, a wet nonwoven fabric can be obtained by cutting the fiber into a fiber length of 10 mm and wet-making with a binder fiber. At this time, as in the case of the production of the dry nonwoven fabric, it may be mixed so that other types of fibers are less than 70% by mass. A wet nonwoven fabric can be obtained by applying a high-pressure water flow of 30 kg / cm 2 or more to a base paper obtained by making a slurry containing at least part of the fiber of the present invention.

上記したような方法にて不織布を製造するが、本発明の目的とする清掃性能を得るためには、不織布を構成する繊維が不織布中において十分に固定されていることが重要であり、そのためには不織布に高分子系樹脂状物が付与されてなるか、あるいは熱融着繊維からなるバインダー繊維を混綿することが好ましい。繊維の固定が不十分であると、清掃用不織布として使用した際、汚れ掻き取り時に繊維が動くため掻き取る力が逃げてしまう。また清掃用不織布としては致命的である清掃後の拭取り対象物への繊維の脱落が発生する。これらの方法による繊維の固定は、不織布の伸長−引張強力曲線の傾きに相関し、固定が進むほど傾きが大きくなるため不織布の伸長時での引張強力が高くなる。つまり、不織布の伸長時での引張強力の高さが、掻き取り性能の指標となる。
図3に不織布の伸度−引張強力曲線の一例を示す。不織布の伸長時での挙動を図3により説明する。一般的な繊維のみによる機械的な絡合で構成された従来の不織布の伸度−引張強力曲線を(A)、本発明の不織布が高分子系樹脂状物あるいは熱融着繊維からなるバインダー繊維で固定された不織布の伸度−引張強力曲線は(B)となる。
本発明の高分子系樹脂状物あるいは熱融着繊維からなるバインダー繊維で固定された不織布(B)は固定されていない従来の(A)に比べ破断伸度が1/2以下となり、同一伸度時の引張強力も高くなる。さらに高分子系樹脂状物あるいは熱融着繊維からなるバインダー繊維で固定された本発明の不織布は伸長後でも回復する領域が大きい。このことは不織布中の繊維が高分子系樹脂状物あるいは熱融着繊維からなるバインダー繊維により固定されていることをより明確に表している。
そこで本発明では、図3における(B)の不織布が伸長後でも回復しうる領域をIとした場合、繊維を固定したまま不織布が伸長回復しうる領域境界である伸度3%時の引張強力を、不織布中の繊維が高分子系樹脂状物あるいは熱融着繊維からなるバインダー繊維によりどの程度固定されているかを示す尺度として定義した。なお、本発明でいう不織布の伸度−引張強力曲線は、後述する方法で得られる。
Although a nonwoven fabric is manufactured by the method as described above, in order to obtain the cleaning performance targeted by the present invention, it is important that the fibers constituting the nonwoven fabric are sufficiently fixed in the nonwoven fabric. It is preferable that the non-woven fabric is provided with a polymer resinous material, or binder fibers made of heat-sealing fibers are mixed. If the fibers are not sufficiently fixed, when used as a cleaning nonwoven fabric, the fibers move when the dirt is scraped off, so that the scraping force escapes. In addition, the loss of fibers to the wiping target after cleaning, which is fatal as a nonwoven fabric for cleaning, occurs. The fixing of the fibers by these methods correlates with the inclination of the elongation-tensile strength curve of the nonwoven fabric, and the inclination increases as the fixing proceeds, so that the tensile strength at the time of elongation of the nonwoven fabric increases. That is, the high tensile strength when the nonwoven fabric is stretched is an index of the scraping performance.
FIG. 3 shows an example of the elongation-tensile strength curve of the nonwoven fabric. The behavior of the nonwoven fabric during elongation will be described with reference to FIG. (A) shows the elongation-tensile strength curve of a conventional nonwoven fabric constructed by mechanical entanglement using only ordinary fibers, and the nonwoven fabric of the present invention is made of a polymer resinous material or a heat-sealed fiber. The elongation-tensile strength curve of the non-woven fabric fixed in (B) is (B).
The non-woven fabric (B) fixed with the binder fiber made of the polymer resin material or heat-bonding fiber of the present invention has a breaking elongation of ½ or less compared to the conventional non-fixed (A), and the same elongation. The tensile strength at the time also increases. Furthermore, the nonwoven fabric of the present invention fixed with a binder fiber made of a polymer resinous material or a heat-sealing fiber has a large recovery area even after elongation. This more clearly indicates that the fibers in the nonwoven fabric are fixed by a binder fiber made of a polymer resinous material or a heat-sealing fiber.
Therefore, in the present invention, when the region where the nonwoven fabric of (B) in FIG. 3 can recover after stretching is defined as I, the tensile strength when the elongation is 3%, which is the region boundary where the nonwoven fabric can stretch and recover with the fibers fixed. Was defined as a scale indicating how much the fibers in the nonwoven fabric are fixed by the binder fibers made of polymer resinous materials or heat-sealing fibers. In addition, the elongation-tensile strength curve of the nonwoven fabric referred to in the present invention is obtained by the method described later.

本発明の高分子系樹脂状物が付与されてなるあるいは熱融着繊維からなるバインダー繊維が混綿されてなる不織布において、十分な繊維の固定を確保し、掻き取り性能を向上させるためには、上記定義した3%伸長時の引張強力が不織布の何れかの方向で1.0kg/25mm以上、好ましくは1.2kg/25mm以上15kg/25mm以下であれば不織布を構成する繊維が不織布中において十分に固定されており、本発明の目的とする清掃用不織布の性能が得られやすい。不織布の3%伸長時の引張強力としては、清掃用不織布の流れ方向(MD)および幅方向(CD)の何れの方向においても、1.0kg/25mm以上となることがより好ましいが、少なくとも一方の方向において1.2kg/25mm以上であれば、十分な掻き取り性能が発現する。一方、3%伸長時の引張強力が1.0kg/25mm未満であると、清掃時の汚れ掻き取り時に不織布中の繊維が十分に固定されていないので、本発明の目的とする掻き取り性能が得られない場合が多い。  In the nonwoven fabric in which the polymer resin-like material of the present invention is applied or the binder fiber composed of the heat-sealing fiber is mixed, in order to ensure sufficient fiber fixation and improve the scraping performance, If the tensile strength at 3% elongation defined above is 1.0 kg / 25 mm or more, preferably 1.2 kg / 25 mm or more and 15 kg / 25 mm or less in any direction of the nonwoven fabric, the fibers constituting the nonwoven fabric are sufficient in the nonwoven fabric. The performance of the nonwoven fabric for cleaning which is the object of the present invention is easily obtained. The tensile strength at 3% elongation of the nonwoven fabric is more preferably 1.0 kg / 25 mm or more in any of the flow direction (MD) and the width direction (CD) of the nonwoven fabric for cleaning, but at least one of them If it is 1.2 kg / 25 mm or more in this direction, sufficient scraping performance is exhibited. On the other hand, if the tensile strength at the time of 3% elongation is less than 1.0 kg / 25 mm, the fibers in the nonwoven fabric are not sufficiently fixed at the time of scraping the dirt at the time of cleaning. In many cases, it cannot be obtained.

本発明の不織布に熱融着繊維からなるバインダー繊維を混綿する場合、熱融着繊維としては、通常の不織布生産工程でバインダー性能を発揮できる繊維ならばよく、ポリエステル系繊維、ポリオレフィン系繊維、ナイロン系繊維、ポリ乳酸系繊維等が例示できるが、特に限定されるものではない。熱融着繊維の混綿量としては10質量%以上であることが好ましく、20質量%以上であることがより好ましい。混綿量が10質量%未満であると十分な繊維の固定ができないので、拭取り性能が低下するだけでなく、清掃用不織布としては致命的となる清掃対象物への繊維の脱落が発生してしまうことがある。  In the case of blending a binder fiber composed of a heat-bonding fiber into the nonwoven fabric of the present invention, the heat-bonding fiber may be any fiber that can exhibit binder performance in a normal nonwoven fabric production process, such as polyester fiber, polyolefin fiber, nylon. Examples of the fiber include polylactic acid fiber and polylactic acid fiber, but are not particularly limited. The blend amount of the heat-sealing fibers is preferably 10% by mass or more, and more preferably 20% by mass or more. If the amount of blended cotton is less than 10% by mass, sufficient fibers cannot be fixed, so that not only the wiping performance is deteriorated, but also the fibers fall into the cleaning object which is fatal as a nonwoven fabric for cleaning. It may end up.

本発明の不織布に高分子系樹脂状物に付与する場合、付与される高分子系樹脂状物としてはレンジ等での高温となる拭取り対象物や、摩擦熱等での温度上昇時でも効果の低下が見られない熱硬化性の樹脂が良く、フェノール樹脂、ユリア樹脂、メラミン樹脂、エポキシ樹脂、あるいはポリアクリル酸等の自己架橋性アクリル系樹脂等を例示できるが、特に限定されるものではない。自己架橋性ではない樹脂の場合、夫々に応じた硬化剤を適量配合し、硬化に必要な熱を供給することが重要である。  When applied to the polymeric resinous material to the nonwoven fabric of the present invention, the applied polymeric resinous material is effective even when the object to be wiped at a high temperature such as in a range or when the temperature rises due to frictional heat, etc. A thermosetting resin in which a decrease in the viscosity is not observed is good, and examples thereof include phenolic resins, urea resins, melamine resins, epoxy resins, and self-crosslinking acrylic resins such as polyacrylic acid, but are not particularly limited. Absent. In the case of a resin that is not self-crosslinkable, it is important to mix an appropriate amount of a curing agent corresponding to each resin and supply heat necessary for curing.

上記高分子系樹脂状物の付着量としては、不織布重量に対して5〜200質量%とすることが好ましい。高分子系樹脂状物の付着効果としては、繊維の固定以外に繊維表面を硬質な高分子系樹脂状物がコーティングされることにより、エッジ効果がより向上する利点がある。上記高分子系樹脂状物の付着量が5質量%未満であると繊維の固定が不十分となり、汚れ除去時に不織布中の繊維が動くため、繊維による掻き取り力が逃げてしまい、十分な掻き取り性能が得られない場合が多い。逆に200質量%を超えると樹脂分が過剰となってしまい、掻き取った汚れを保持する空間を埋めてしまい、汚れ成分により拭取り面への接触が阻害されてしまうことがある。より好ましくは10〜150質量%であり、さらに好ましくは20〜100質量%である。20質量%以上になると高分子系樹脂状物により繊維表面をコートする部分が増加することによりエッジ効果を増強し、掻き取り効果をより一層向上させるので好ましい。  The adhesion amount of the polymer resinous material is preferably 5 to 200% by mass with respect to the weight of the nonwoven fabric. The adhesion effect of the polymer resinous material has an advantage that the edge effect is further improved by coating the fiber surface with a hard polymer resinous material in addition to fixing the fiber. If the amount of the polymeric resinous material attached is less than 5% by mass, the fibers will not be fixed sufficiently, and the fibers in the nonwoven fabric will move when removing the dirt. In many cases, the performance cannot be obtained. On the other hand, if it exceeds 200% by mass, the resin content becomes excessive, filling the space for holding the scraped dirt, and the dirt component may inhibit the contact with the wiping surface. More preferably, it is 10-150 mass%, More preferably, it is 20-100 mass%. When the content is 20% by mass or more, the portion that coats the fiber surface with the polymer resinous material is increased, thereby enhancing the edge effect and further improving the scraping effect.

上記高分子系樹脂状物の付着方法としては、前述の樹脂からなる溶液やモノマーを使用し、不織布の繊維表面および交絡部に付着させて溶媒を蒸発させるか、あるいは繊維上で重合固化させるのが好ましい。前記した高分子系樹脂状物には、必要に応じて研磨剤を添加し、該樹脂を乾燥させると同時に研磨剤を不織布に固着させたり、高分子系樹脂状物を不織布に被覆し、乾燥させる前に研磨剤を散布して不織布に固着させてもよい。研磨剤を併用することにより掻き取り効果が向上し、こびりついた汚れなどの掻き取り性能が大幅に向上する。研磨剤としては、公知の研磨剤であれば特に限定されず、例えばアルミナ、珪藻土、シリカ、炭酸カルシウム、リン酸カルシウム、カーボランダム、金剛砂、ガラスビーズ、雲母などが挙げられる。研磨剤の大きさ、形状は使用する用途に応じて設定すればよいが、粒径5μm以下の粒子を用いることが好ましい。  As a method for attaching the polymer resinous material, a solution or a monomer made of the above-described resin is used, and the solvent is evaporated by adhering to the fiber surface and the entangled part of the nonwoven fabric, or polymerized and solidified on the fiber. Is preferred. Abrasives are added to the above-described polymer-based resinous material as necessary, and the resin is dried, and at the same time, the abrasive is fixed to the nonwoven fabric, or the polymer-based resinous material is coated on the nonwoven fabric and dried. Before making it, you may spray an abrasive | polishing agent and you may make it adhere to a nonwoven fabric. By using an abrasive together, the scraping effect is improved, and the scraping performance such as sticking dirt is greatly improved. The abrasive is not particularly limited as long as it is a known abrasive, and examples thereof include alumina, diatomaceous earth, silica, calcium carbonate, calcium phosphate, carborundum, gold sand, glass beads, mica and the like. The size and shape of the abrasive may be set according to the intended use, but it is preferable to use particles having a particle size of 5 μm or less.

以下実施例により、本発明を詳細に説明するが、本発明は実施例により何等制限されるものではない。なお、本発明の実施例において、繊維の扁平度、繊維表面に存在する溝の本数・溝の深さ、3%伸長時の引張強力、繊維の脱落性、清掃性能及び清掃時のキズ付き性は以下の測定法にて測定されたものとする。  Hereinafter, the present invention will be described in detail by way of examples. However, the present invention is not limited to the examples. In the examples of the present invention, the flatness of the fiber, the number of grooves existing on the fiber surface, the depth of the groove, the tensile strength when stretched by 3%, the fiber falling off, the cleaning performance, and the scratching property during cleaning Is measured by the following measurement method.

[繊維の扁平度]
繊維断面を走査型電子顕微鏡(株式会社日立製作所製「S−510」)で1000倍の倍率により撮影した写真により繊維断面における長辺と短辺の長さを測定し、扁平度を下記式より算出し、繊維20本の平均値として表した。
扁平度=長辺の長さ/短辺の長さ
[Fiber flatness]
The length of the long side and the short side of the fiber cross section are measured by a photograph obtained by taking a cross section of the fiber with a scanning electron microscope (“S-510” manufactured by Hitachi, Ltd.) at a magnification of 1000 times. Calculated and expressed as an average value of 20 fibers.
Flatness = Long side length / Short side length

[繊維表面に存在する溝の本数、溝の深さ]
繊維断面を走査型電子顕微鏡(株式会社日立製作所製「S−510」)で3000倍の倍率により撮影した写真により、繊維外周部分における外周部10μmあたりの溝の本数、および溝の深さを測定し、繊維20本の平均値として表した。
[Number of grooves on the fiber surface, depth of grooves]
The number of grooves per 10 μm of the outer periphery of the outer periphery of the fiber and the depth of the groove are measured with a photograph taken with a scanning electron microscope (“S-510” manufactured by Hitachi, Ltd.) at a magnification of 3000 times. And expressed as an average value of 20 fibers.

[3%伸長時の引張強力 kg/25mm]
JIS L1096の引張強力測定法に準拠して、不織布のMD方向25mm幅の試験片を作製し、図3に示すような伸び−引張強力曲線を測定し、得られた測定曲線より3%伸長時の引張強力を求めた。
[Tensile strength at 3% elongation kg / 25mm]
In accordance with the tensile strength measurement method of JIS L1096, a test piece having a width of 25 mm in the MD direction of the nonwoven fabric was prepared, an elongation-tensile strength curve as shown in FIG. 3 was measured, and the elongation was 3% from the obtained measurement curve. The tensile strength of was determined.

[繊維の脱落性]
清掃性能評価時の繊維脱落有無により判断した。
[Fabricity of fibers]
Judgment was made based on the presence or absence of fiber dropout during the cleaning performance evaluation.

[清掃性能]
不織布を5cm×5cmにカットし、透明なアクリル板上に墨汁を0.15ml滴下したものを200gの錘を載せて拭取り、拭取り後のアクリル板を色差計(日本電色工業株式会社製「Z−300A」)で透過率を測定し、透過率が80%以上の場合、清掃性能を良好(○)と評価した。
[Cleaning performance]
Cut non-woven fabric into 5cm x 5cm, drop 0.15ml of ink on a transparent acrylic plate, wipe it with 200g weight, and wipe the acrylic plate after wiping the color difference meter (manufactured by Nippon Denshoku Industries Co., Ltd.) The transmittance was measured with “Z-300A”), and when the transmittance was 80% or more, the cleaning performance was evaluated as good (◯).

[清掃時キズ付き性]
不織布を5cm×5cmにカットしたものに200%/不織布の水分を含浸させ、摩擦堅牢度試験機にOHPシート(コクヨ社製「VF−1」)を取り付け、前記不織布で200回摩擦し、摩擦後のOHPシートへのキズの有無を目視観察し、評価した。
[Scratch when cleaning]
A non-woven fabric cut to 5 cm × 5 cm is impregnated with 200% / non-woven fabric moisture, an OHP sheet (“VF-1” manufactured by KOKUYO) is attached to a friction fastness tester, and the non-woven fabric is rubbed 200 times to rub. The presence or absence of scratches on the subsequent OHP sheet was visually observed and evaluated.

[実施例1]
(1)平均重合度1700、ケン化度99.9モル%のPVAポリマー15質量%および層状化合物(コープケミカル株式会社社製合成雲母「MEB−3」)2.0質量%の水溶液からなる紡糸原液を孔数4000、縦30μm×横450μmの長方形のスリット型の紡糸口金より飽和硫酸ナトリウムからなる凝固浴中に吐出させ、第1ローラーで巻き取り、4倍の湿延伸を行った後、130℃で乾燥を行った。引続き230℃で2倍の乾熱延伸を行い、単繊維繊度1.2dtex、扁平度15、繊維外周長手方向10μm間隔に深さ0.3μmの溝が3個存在する、図1に示すような形状のPVA繊維を得た。得られたPVA繊維をホルムアルデヒド5質量%、硫酸10質量%からなる水溶液中で60分間アセタール化処理を行った。
(2)上記(1)で得られたPVA繊維を10mmにカットし、さらにカットしたPVA繊維と2.2dtex×10mmのポリエステル系バインダー繊維(株式会社クラレ製「N720」)とをPVA繊維/ポリエステル繊維=80/20(質量比)の組成にて混合し、目付30g/mの湿式不織布を製造した。続いて水流絡合装置により水圧60kg/mで絡合処理した。
(3)得られた不織布の性能評価結果を表1に示す。得られた不織布の3%伸長時の引張強力は1.4kg/25mmであり、不織布中において繊維がバインダーにより十分に固定されているのが確認できた。またこのようにして得られた不織布において繊維の脱落はなく、清掃性は良好で清掃時にキズ付きはみられなかった。
[Example 1]
(1) Spinning comprising an aqueous solution of 15% by mass of PVA polymer having an average polymerization degree of 1700 and a saponification degree of 99.9% by mole and a layered compound (synthetic mica “MEB-3” manufactured by Corp Chemical Co., Ltd.) of 2.0% by mass. The stock solution was discharged into a coagulation bath made of saturated sodium sulfate from a rectangular slit-type spinneret having a number of holes of 4000, length of 30 μm × width of 450 μm, wound with a first roller, subjected to wet stretching four times, and then 130 Drying was performed at ° C. Subsequently, dry heat drawing is performed twice at 230 ° C., and there are three grooves each having a single fiber fineness of 1.2 dtex, a flatness of 15, and a depth of 10 μm in the fiber outer circumferential direction at a depth of 0.3 μm, as shown in FIG. A shaped PVA fiber was obtained. The obtained PVA fiber was acetalized for 60 minutes in an aqueous solution consisting of 5% by mass of formaldehyde and 10% by mass of sulfuric acid.
(2) The PVA fiber obtained in the above (1) is cut to 10 mm, and the cut PVA fiber and 2.2 dtex × 10 mm polyester binder fiber (“N720” manufactured by Kuraray Co., Ltd.) are PVA fiber / polyester. A wet nonwoven fabric with a basis weight of 30 g / m 2 was produced by mixing at a composition of fiber = 80/20 (mass ratio). Subsequently, an entanglement treatment was performed at a water pressure of 60 kg / m 2 using a water entanglement device.
(3) Table 1 shows the performance evaluation results of the obtained nonwoven fabric. The tensile strength at 3% elongation of the obtained nonwoven fabric was 1.4 kg / 25 mm, and it was confirmed that the fibers were sufficiently fixed by the binder in the nonwoven fabric. In addition, the nonwoven fabric obtained in this manner had no fibers falling off, had good cleaning properties, and was not scratched during cleaning.

[実施例2]
不織布の繊維組成をPVA繊維/ポリエステル繊維=50/50(質量比)に変更すること以外は実施例1と同様の条件にて不織布を得た。得られた不織布の性能評価結果を表1に示す。得られた不織布は実施例1と同様、繊維の脱落がなく、清掃性及び清掃時のキズ付き性が良好であった。
[Example 2]
A nonwoven fabric was obtained under the same conditions as in Example 1 except that the fiber composition of the nonwoven fabric was changed to PVA fiber / polyester fiber = 50/50 (mass ratio). The performance evaluation results of the obtained nonwoven fabric are shown in Table 1. As in Example 1, the obtained nonwoven fabric had no fibers falling off, and had good cleaning properties and scratching properties during cleaning.

[実施例3]
平均重合度1700、ケン化度99.9モル%のPVAポリマー15質量%および層状化合物(コープケミカル株式会社製合成雲母「MEB−3」)2.0質量%の水溶液からなる紡糸原液を孔数4000、縦50μm×横300μmの長方形のスリット型の紡糸口金より飽和硫酸ナトリウムからなる凝固浴中に吐出させ、第1ローラーで巻き取り、4倍の湿延伸を行った後、130℃で乾燥を行った。引続き230℃で2倍の乾熱延伸を行い、単繊維繊度1.3dtex、扁平度6、繊維外周長手方向10μm間隔に深さ0.3μmの溝が3個存在する、図1に示すような形状のPVA繊維を得た。得られたPVA繊維をホルムアルデヒド5質量%、硫酸10質量%からなる水溶液中で60分間アセタール化処理を行った。
その後、該繊維を用いて実施例1と同様の条件で不織布を製造した。得られた不織布の性能評価結果を表1に示す。得られた不織布は実施例1と同様、繊維の脱落がなく、清掃性及び清掃時のキズ付き性が良好であった。
[Example 3]
A spinning stock solution comprising an aqueous solution of 15% by mass of PVA polymer having an average degree of polymerization of 1700 and a saponification degree of 99.9% by mol and a layered compound (synthetic mica “MEB-3” manufactured by Coop Chemical Co., Ltd.) is 2.0% by mass. 4000, length 50μm × width 300μm rectangular slit type spinneret is discharged into a coagulation bath consisting of saturated sodium sulfate, wound with the first roller, 4 times wet stretching, and then dried at 130 ° C went. Subsequently, dry heat drawing is performed twice at 230 ° C., and there are three grooves each having a single fiber fineness of 1.3 dtex, a flatness of 6, and a depth of 10 μm in the fiber outer circumferential direction at a depth of 0.3 μm, as shown in FIG. A shaped PVA fiber was obtained. The obtained PVA fiber was acetalized for 60 minutes in an aqueous solution consisting of 5% by mass of formaldehyde and 10% by mass of sulfuric acid.
Then, the nonwoven fabric was manufactured on the conditions similar to Example 1 using this fiber. The performance evaluation results of the obtained nonwoven fabric are shown in Table 1. As in Example 1, the obtained nonwoven fabric had no fibers falling off, and had good cleaning properties and scratching properties during cleaning.

[実施例4]
(1)平均重合度1700、ケン化度99.9モル%のPVAポリマー15質量%および層状化合物(コープケミカル株式会社製合成雲母「MEB−3」)2.0質量%の水溶液からなる紡糸原液を孔数4000、縦30μm×横450μmの長方形のスリット型の紡糸口金より飽和硫酸ナトリウムからなる凝固浴中に吐出させ、第1ローラーで巻き取り、4倍の湿延伸を行った後、130℃で乾燥を行った。引続き230℃で2倍の乾熱延伸を行い、単繊維繊度1.2dtex、扁平度15、繊維外周長手方向10μm間隔に深さ0.3μmの溝が3個存在する、図1に示すような形状のPVA繊維を得た。得られたPVA繊維をホルムアルデヒド5質量%、硫酸10質量%からなる水溶液中で60分間アセタール化処理を行った。
(2)上記(1)で得られたPVA繊維を10mmにカットし、目付30g/mの湿式不織布を製造した。続いて水流絡合装置により水圧60kg/cmで絡合処理し、不織布に対し20質量%付着するように熱硬化性アクリル系樹脂(BASF社製「アクロデュア945L」)を含浸し、エアースルー式乾燥機中120℃で予備乾燥後、200℃でキュア処理を行った。得られた不織布の性能評価結果を表1に示す。得られた不織布の3%伸長時の引張強力は2.8kg/25mmであり、繊維の固定及び不織布表面をコートするように樹脂が付着しているのを確認した。また、このようにして得られた不織布において、繊維の脱落はなく、清掃性及び清掃時のキズ付き性が良好であった。
[Example 4]
(1) Spinning stock solution comprising an aqueous solution of 15% by mass of a PVA polymer having an average degree of polymerization of 1700 and a saponification degree of 99.9 mol% and a layered compound (synthetic mica “MEB-3” manufactured by Coop Chemical Co., Ltd.) Is discharged into a coagulation bath made of saturated sodium sulfate from a rectangular slit-type spinneret having a pore number of 4000, length of 30 μm × width of 450 μm, wound with a first roller, subjected to wet stretching four times, and then 130 ° C. And dried. Subsequently, dry heat drawing is performed twice at 230 ° C., and there are three grooves each having a single fiber fineness of 1.2 dtex, a flatness of 15, and a depth of 10 μm in the fiber outer circumferential direction at a depth of 0.3 μm, as shown in FIG. A shaped PVA fiber was obtained. The obtained PVA fiber was acetalized for 60 minutes in an aqueous solution consisting of 5% by mass of formaldehyde and 10% by mass of sulfuric acid.
(2) The PVA fiber obtained in the above (1) was cut to 10 mm to produce a wet nonwoven fabric with a basis weight of 30 g / m 2 . Subsequently, the water entanglement device is entangled at a water pressure of 60 kg / cm 2 , impregnated with a thermosetting acrylic resin (“Acrodure 945L” manufactured by BASF) so as to adhere to 20% by mass of the nonwoven fabric, and is an air-through type. After preliminary drying at 120 ° C. in a dryer, curing treatment was performed at 200 ° C. The performance evaluation results of the obtained nonwoven fabric are shown in Table 1. The tensile strength at 3% elongation of the obtained nonwoven fabric was 2.8 kg / 25 mm, and it was confirmed that the resin was adhered so as to fix the fibers and coat the surface of the nonwoven fabric. Moreover, in the nonwoven fabric obtained in this way, the fiber did not fall off, and the cleaning property and scratching property during cleaning were good.

[実施例5]
不織布への熱硬化性アクリル樹脂の付着量を不織布に対し5質量%とすること以外は実施例4と同様に不織布を得た。得られた不織布の性能評価結果を表1に示す。得られた不織布は実施例1と同様、清掃性及び清掃時のキズ付き性が良好であった。
[Example 5]
A nonwoven fabric was obtained in the same manner as in Example 4 except that the adhesion amount of the thermosetting acrylic resin to the nonwoven fabric was 5 mass% with respect to the nonwoven fabric. The performance evaluation results of the obtained nonwoven fabric are shown in Table 1. As in Example 1, the obtained nonwoven fabric had good cleaning properties and scratching properties during cleaning.

[実施例6]
不織布の繊維組成をPVA繊維、レーヨン(ダイワボウ社製「コロナ」、1.1dtex×7mm)、ポリエステル系バインダー繊維とし、それらの比率をPVA繊維/レーヨン/ポリエステル繊維=50/10/40(質量比)とすること以外は実施例1と同様の製造方法にて不織布を得た。得られた不織布の性能評価結果を表1に示す。得られた不織布の3%伸長時の引張強力は2.3kg/25mmであり、また実施例1と同様、繊維の脱落がなく、清掃性及び清掃時のキズ付き性が良好であった。
[Example 6]
The fiber composition of the nonwoven fabric is PVA fiber, rayon (“Corona” manufactured by Daiwabo Co., Ltd., 1.1 dtex × 7 mm), and polyester binder fiber, and the ratio thereof is PVA fiber / rayon / polyester fiber = 50/10/40 (mass ratio). The nonwoven fabric was obtained by the same production method as in Example 1 except that. The performance evaluation results of the obtained nonwoven fabric are shown in Table 1. The obtained nonwoven fabric had a tensile strength at 3% elongation of 2.3 kg / 25 mm, and, as in Example 1, there was no fiber dropout, and the cleaning property and scratching property during cleaning were good.

[実施例7]
不織布の繊維組成をPVA繊維、ポリ乳酸繊維(株式会社クラレ製、1.8dtex×10mm)、ポリエステル系バインダー繊維とし、それらの比率をPVA繊維/ポリ乳酸繊維/ポリエステル繊維=60/20/20(質量比)とすること以外は実施例1と同様の製造方法にて不織布を得た。得られた不織布の性能評価結果を表1に示す。得られた不織布の3%伸長時の引張強力は1.5kg/25mmであり、また実施例1と同様、繊維の脱落がなく、清掃性及び清掃時のキズ付き性が良好であった。
[Example 7]
The fiber composition of the nonwoven fabric is PVA fiber, polylactic acid fiber (manufactured by Kuraray Co., Ltd., 1.8 dtex × 10 mm), and polyester binder fiber, and the ratio thereof is PVA fiber / polylactic acid fiber / polyester fiber = 60/20/20 ( A non-woven fabric was obtained by the same production method as in Example 1 except that the mass ratio). The performance evaluation results of the obtained nonwoven fabric are shown in Table 1. The tensile strength at 3% elongation of the obtained non-woven fabric was 1.5 kg / 25 mm, and as in Example 1, there was no fiber dropout, and the cleaning property and scratching property during cleaning were good.

[比較例1]
平均重合度1700、ケン化度99.9モル%のPVAポリマー17質量%および層状化合物(コープケミカル株式会社製合成雲母「MEB−3」)0.3質量%の水溶液からなる紡糸原液を実施例1とノズル形状を変更した孔数4000、縦70μm×横210μmの長方形のスリット型の紡糸口金より飽和硫酸ナトリウムからなる凝固浴中に吐出させ、第1ローラーで巻き取り、4倍の湿延伸を行った後、130℃で乾燥を行った。引続き230℃で2倍の乾熱延伸を行い、単繊維繊度1.3dtex、扁平度3、繊維外周長手方向10μm間隔に深さ0.05μmの溝が1個存在する、扁平度が小さく溝の浅い形状のPVA繊維を得た。得られたPVA繊維をホルムアルデヒド5質量%、硫酸10質量%からなる水溶液中で60分間アセタール化処理を行った。
その後、該繊維を用いて実施例1と同様の方法で不織布を製造した。得られた不織布の性能評価結果を表2に示す。得られた不織布は、清掃時のキズ付き性は良好であったが、不織布を構成するPVA繊維の扁平度が3と低く、溝の浅い形状であったため、清掃性が劣るものであった。
[Comparative Example 1]
Spinning stock solution comprising an aqueous solution of 17% by mass of PVA polymer having an average degree of polymerization of 1700 and a saponification degree of 99.9% by mol and a layered compound (synthetic mica “MEB-3” manufactured by Corp Chemical Co., Ltd.) of 0.3% by mass 1 and the nozzle shape is changed to 4000, the length is 70μm × width 210μm rectangular slit-type spinneret is discharged into a coagulation bath made of saturated sodium sulfate, wound with the first roller, 4 times wet stretch After performing, it dried at 130 degreeC. Subsequently, dry heat stretching is performed twice at 230 ° C., and there is a single fiber fineness of 1.3 dtex, flatness of 3, and one groove having a depth of 0.05 μm at intervals of 10 μm in the fiber outer peripheral longitudinal direction. A shallow PVA fiber was obtained. The obtained PVA fiber was acetalized for 60 minutes in an aqueous solution consisting of 5% by mass of formaldehyde and 10% by mass of sulfuric acid.
Then, the nonwoven fabric was manufactured by the method similar to Example 1 using this fiber. The performance evaluation results of the obtained nonwoven fabric are shown in Table 2. The obtained nonwoven fabric had good scratching properties during cleaning, but the flatness of the PVA fibers constituting the nonwoven fabric was as low as 3 and the groove was shallow, so the cleaning properties were inferior.

[比較例2]
平均重合度1700、ケン化度99.9モル%のPVAポリマー15質量%、ホウ酸0.3質量%の水溶液からなる紡糸原液を孔数4000、縦30μm×横450μmの長方形のスリット型の紡糸口金よりpH12以上に調製した飽和硫酸ナトリウムからなる凝固浴中に吐出させ、第1ローラーで巻き取り、4倍の湿延伸を行った後、130℃で乾燥を行った。引続き230℃で3倍の乾熱延伸を行い、単繊維繊度1.5dtex、扁平度15の繊維表面に溝のないPVA繊維を得た。得られたPVA繊維をホルムアルデヒド5質量%、硫酸10質量%からなる水溶液中で60分間アセタール化処理を行った。
その後、該繊維を用いて実施例1と同様の条件にて不織布を得た。得られた不織布の性能評価結果を表2に示す。得られた不織布は、清掃時のキズ付き性は良好であったが、不織布を構成するPVA繊維の外周長手方向に溝が形成されていないため、清掃性が劣るものであった。
[Comparative Example 2]
A rectangular slit-type spinning of a spinning stock solution consisting of an aqueous solution of an average degree of polymerization of 1700, a PVA polymer of 15% by mass and a saponification degree of 99.9% by mol and boric acid of 0.3% by mass with a pore size of 4000, length 30 μm × width 450 μm. It was discharged from a die into a coagulation bath made of saturated sodium sulfate adjusted to pH 12 or higher, wound with a first roller, subjected to wet stretching four times, and then dried at 130 ° C. Subsequently, dry heat drawing was performed 3 times at 230 ° C. to obtain a PVA fiber having a single fiber fineness of 1.5 dtex and a flatness of 15 and having no grooves on the fiber surface. The obtained PVA fiber was acetalized for 60 minutes in an aqueous solution consisting of 5% by mass of formaldehyde and 10% by mass of sulfuric acid.
Then, the nonwoven fabric was obtained on the conditions similar to Example 1 using this fiber. The performance evaluation results of the obtained nonwoven fabric are shown in Table 2. Although the obtained nonwoven fabric had good scratchability at the time of cleaning, since the groove was not formed in the outer peripheral longitudinal direction of the PVA fiber constituting the nonwoven fabric, the cleaning property was inferior.

[比較例3]
不織布の繊維組成をPVA繊維/ポリエステル系バインダー繊維=20/80(質量比)に変更すること以外は、実施例1と同様の条件にて不織布を得た。得られた不織布の性能評価結果を表2に示す。得られた不織布は清掃時のキズ付き性は良好であったが、不織布を構成するPVA繊維の含有比率が低いため、清掃性が劣るものであった。
[Comparative Example 3]
A nonwoven fabric was obtained under the same conditions as in Example 1 except that the fiber composition of the nonwoven fabric was changed to PVA fiber / polyester binder fiber = 20/80 (mass ratio). The performance evaluation results of the obtained nonwoven fabric are shown in Table 2. Although the obtained nonwoven fabric had good scratching property at the time of cleaning, since the content ratio of the PVA fibers constituting the nonwoven fabric was low, the cleaning property was inferior.

[比較例4]
不織布の繊維組成をPVA繊維/ポリエステル系バインダー繊維=95/5(質量比)に変更すること以外は実施例1と同様の条件にて不織布を得た。得られた不織布の性能評価結果を表2に示す。得られた不織布は清掃時のキズ付き性および清掃性は良好であるが、不織布を構成するバインダー繊維の混綿率が低いため繊維の脱落が発生し、清掃用不織布としては不適であった。
[Comparative Example 4]
A nonwoven fabric was obtained under the same conditions as in Example 1 except that the fiber composition of the nonwoven fabric was changed to PVA fiber / polyester binder fiber = 95/5 (mass ratio). The performance evaluation results of the obtained nonwoven fabric are shown in Table 2. The obtained non-woven fabric was excellent in scratching and cleaning properties at the time of cleaning. However, since the blending rate of the binder fibers constituting the non-woven fabric was low, the fibers dropped out and was unsuitable as a non-woven fabric for cleaning.

[比較例5]
不織布への熱硬化性アクリル樹脂の付着量を不織布に対し3質量%とすること以外は実施例4と同様に不織布を得た。得られた不織布の性能評価結果を表2に示す。得られた不織布は、清掃時のキズ付き性および清掃性は良好であったが、不織布に付与する熱硬化性アクリル樹脂の付着量が少ないため繊維の脱落が発生し、清掃用不織布としては不適であった。
[Comparative Example 5]
A nonwoven fabric was obtained in the same manner as in Example 4 except that the amount of the thermosetting acrylic resin attached to the nonwoven fabric was 3% by mass with respect to the nonwoven fabric. The performance evaluation results of the obtained nonwoven fabric are shown in Table 2. The obtained non-woven fabric was excellent in scratching and cleaning properties at the time of cleaning, but the amount of the thermosetting acrylic resin applied to the non-woven fabric is small, so that the fibers fall off and is not suitable as a non-woven fabric for cleaning. Met.

[比較例5]
研磨粒子付きスポンジ(住友スリーエム株式会社製「スコッチブライト」)を実施例1と同様に評価したところ、清掃性は良好であるが、多数のキズが拭き取り対象物に残り、キズ付き性は不良であった。性能評価結果を表2に示す。
[Comparative Example 5]
A sponge with abrasive particles (“Scotch Bright” manufactured by Sumitomo 3M Limited) was evaluated in the same manner as in Example 1. As a result, cleanability was good, but many scratches remained on the object to be wiped off, and scratch resistance was poor. there were. The performance evaluation results are shown in Table 2.

Figure 2006095623
Figure 2006095623

Figure 2006095623
Figure 2006095623

表1の実施例1〜5に示すように、本発明の扁平度が6以上の扁平形状であり、かつ繊維断面の外周において繊維の外周長手方向に溝が形成されたPVA繊維を30質量%以上含有した不織布や、さらに熱硬化性アクリル系樹脂を5質量%以上付与してなる不織布は清掃時に繊維の脱落がなく、さらに清掃性および清掃時のキズ付き性に優れたものとなる。
一方、表2に示すように比較例1の扁平度が6未満で繊維外周部分に形成する溝が浅いPVA繊維を用いた不織布、比較例2の繊維外周部分に溝が存在しないPVA繊維を用いた不織布、比較例3の不織布中におけるPVA繊維の含有率が30質量%未満である不織布、比較例4の不織布中にバインダー繊維を混綿した場合、バインダー繊維の混綿量が10質量%未満である場合、さらに比較例5の不織布への熱硬化性アクリル樹脂の付着量を不織布に対し5質量%未満である不織布は共に清掃時のキズ付き性は良好であったが、清掃性が本発明の不織布に比べて劣るものであったり、清掃時に繊維の脱落が見られ、清掃用不織布として適さなかった。さらに比較例5のように市販の研磨粒子付きスポンジの場合は清掃性は良好であったが、多数のキズが拭き取り対象物に残り、キズ付き性は不良であった。
As shown in Examples 1 to 5 in Table 1, 30% by mass of PVA fiber having a flatness of 6 or more according to the present invention and having grooves formed in the outer peripheral longitudinal direction of the fiber at the outer periphery of the fiber cross section. The non-woven fabric contained above or a non-woven fabric formed by applying 5% by mass or more of a thermosetting acrylic resin does not lose fibers during cleaning, and is excellent in cleaning properties and scratching properties during cleaning.
On the other hand, as shown in Table 2, a non-woven fabric using PVA fibers having a flatness of less than 6 in Comparative Example 1 and a shallow groove formed in the fiber outer peripheral portion, and PVA fibers having no groove in the outer peripheral portion of Comparative Example 2 are used. When the binder fiber was mixed in the nonwoven fabric having the PVA fiber content of less than 30% by mass in the nonwoven fabric of Comparative Example 3 and the nonwoven fabric of Comparative Example 4, the blended amount of the binder fiber was less than 10% by mass. In this case, the nonwoven fabric in which the adhesion amount of the thermosetting acrylic resin to the nonwoven fabric of Comparative Example 5 was less than 5% by mass with respect to the nonwoven fabric was good in scratching property at the time of cleaning. It was inferior to the non-woven fabric, or fibers were dropped during cleaning, and was not suitable as a non-woven fabric for cleaning. Further, in the case of the commercially available sponge with abrasive particles as in Comparative Example 5, the cleanability was good, but many scratches remained on the object to be wiped off, and the scratchability was poor.

本発明によれば、清掃性に優れると共に拭き取り対象物にキズが付かない、優れた清掃能力を有する不織布を提供することが可能であり、特にわずかな油汚れから茶渋、水垢あるいはピッチ系の頑固にこびりついた汚れまで洗剤を用いなくても容易に除去することができる。  According to the present invention, it is possible to provide a non-woven fabric having excellent cleaning ability and excellent cleaning ability and having no wiping on the object to be wiped. Even sticky dirt can be easily removed without using a detergent.

本発明の清掃用不織布に用いられるPVA系繊維の断面形状を示す顕微鏡写真。The microscope picture which shows the cross-sectional shape of the PVA type fiber used for the nonwoven fabric for cleaning of this invention. 従来の繭型の断面形状のPVA系繊維を用いた清掃用不織布を示す顕微鏡写真。The microscope picture which shows the nonwoven fabric for cleaning using the conventional saddle-shaped cross-sectional shape PVA type fiber. 不織布の伸度−引張強力曲線の一例を示す図。The figure which shows an example of the elongation-tensile strength curve of a nonwoven fabric.

Claims (8)

繊維断面が扁平形状しており、その断面において扁平度が6〜30であり、かつ繊維の外周長手方向に溝が形成してなるポリビニルアルコール系繊維が30質量%以上含有されてなる不織布で構成される清掃用不織布。  The cross section of the fiber has a flat shape, the flatness is 6 to 30 in the cross section, and the non-woven fabric is composed of 30% by mass or more of polyvinyl alcohol fiber formed with grooves in the longitudinal direction of the outer periphery of the fiber. Nonwoven fabric for cleaning. ポリビニルアルコール系繊維が、繊維の外周長手方向に深さ0.1〜2.0μmの溝が10μm間隔以内に1個以上有する繊維である請求項1記載の清掃用不織布。  The non-woven fabric for cleaning according to claim 1, wherein the polyvinyl alcohol fiber is a fiber having at least one groove having a depth of 0.1 to 2.0 µm within a distance of 10 µm in the longitudinal direction of the outer periphery of the fiber. ポリビニルアルコール系繊維の単繊維繊度が0.5〜5dtex、繊維長が5〜80mmである請求項1または2記載の清掃用不織布。  The nonwoven fabric for cleaning according to claim 1 or 2, wherein the polyvinyl alcohol fiber has a single fiber fineness of 0.5 to 5 dtex and a fiber length of 5 to 80 mm. ポリビニルアルコール系繊維が平均粒子径0.01〜30μmの層状化合物を0.5〜30質量%含有されてなる繊維である請求項1〜3のいずれか1項記載の清掃用不織布。  The nonwoven fabric for cleaning according to any one of claims 1 to 3, wherein the polyvinyl alcohol fiber is a fiber containing 0.5 to 30% by mass of a layered compound having an average particle size of 0.01 to 30 µm. 不織布のいずれかの方向での3%伸長時の引張強力が1.0kg/25mm以上である請求項1〜4のいずれか1項記載の清掃用不織布。  The nonwoven fabric for cleaning according to any one of claims 1 to 4, wherein a tensile strength at 3% elongation in any direction of the nonwoven fabric is 1.0 kg / 25 mm or more. 熱融着繊維からなるバインダー繊維を10質量%以上混綿してなる請求項1〜5のいずれか1項記載の清掃用不織布。  The nonwoven fabric for cleaning according to any one of claims 1 to 5, which is formed by blending 10% by mass or more of binder fibers composed of heat-sealing fibers. 高分子系樹脂状物を不織布重量に対して5〜200質量%付与してなる請求項1〜5のいずれか1項記載の清掃用不織布。   The cleaning nonwoven fabric according to any one of claims 1 to 5, wherein the polymer resinous material is provided in an amount of 5 to 200 mass% based on the weight of the nonwoven fabric. 不織布に付与してなる高分子系樹脂状物が熱硬化性樹脂からなる請求項7記載の清掃用不織布。
The nonwoven fabric for cleaning according to claim 7, wherein the polymer resin material applied to the nonwoven fabric comprises a thermosetting resin.
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JP2016197164A (en) * 2015-04-03 2016-11-24 日本バイリーン株式会社 Fixing part cleaning sheet, fixing part cleaning member, and fixing part cleaning device

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