JP4930985B2 - Manufacturing method and product of fiber material with functional fine particles fixed - Google Patents
Manufacturing method and product of fiber material with functional fine particles fixed Download PDFInfo
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Description
本発明は、熱水により繊維間に空隙を発生させて柔軟性を有する繊維表面に、抗菌剤のような機能性微粒子を接着剤の使用なしに湿熱接着して柔軟性の繊維素材を製造する方法に関する。
さらに詳しくは、本発明は、湿熱接着繊維を平行に配列されたスライバーを用いて、熱水により発生したクリンプ収縮により空隙を生じるとともに該繊維素材の表面に微粒子の少なくとも一部が湿熱接着することによって繊維表面に微粒子よる多くの突起が突出し、各微粒子の本来機能を発揮するようにした柔軟性繊維素材を製造する方法に関する。
The present invention produces flexible fiber materials by generating voids between fibers with hot water and adhering functional fine particles such as antibacterial agents to the surface of the flexible fibers without using an adhesive. Regarding the method.
More specifically, the present invention uses a sliver in which wet-heat bonded fibers are arranged in parallel to form voids due to crimp contraction generated by hot water, and at least some of the fine particles are wet-heat bonded to the surface of the fiber material. It relates to a method for producing a flexible fiber material in which a large number of protrusions due to fine particles protrude from the surface of the fiber so that the original function of each fine particle is exhibited.
従来、機能性効果を有する微粒子を繊維に固着することによって、該微粒子の有する固有の機能を活用した繊維製品は公知であるが、微粒子を繊維に固着する従来技術としては、繊維の中に混合して紡糸する手段と、繊維表面に固着する手段とが知られている。
前者の混合紡糸には、例えば特開平03−205436号公報、特開昭62−195037号公報があり、合成繊維のポリマーに5μm以下の銀系抗菌剤の微粒子を混合して紡糸する方法がある。
Conventionally, fiber products utilizing the inherent function of fine particles by fixing fine particles having a functional effect to the fiber are known. However, as a conventional technique for fixing fine particles to the fiber, mixing is performed in the fiber. Thus, means for spinning and means for fixing to the fiber surface are known.
The former mixed spinning includes, for example, JP-A Nos. 03-205436 and 62-195037, and there is a method in which fine particles of a silver antibacterial agent having a size of 5 μm or less are mixed with a synthetic fiber polymer and then spun. .
上述する従来の微粒子の繊維に固着する手段は、製造工程の煩雑さに加え、混合紡糸により抗菌剤微粒子の多くが繊維の内部に存在したままとなり、繊維表面に必要な抗菌剤微粒子のブリーディングが少なくなるので、漸次、薬剤が外部に滲出してくることによって抗菌効果が発揮され難いという問題がある。
後者の後加工には、接着剤を用いて繊維製品に担持する方法が一般的で、代表的には、特開平02−021916号公報の技術がある。しかしながら、この技術では、微粒子が接着剤に包埋されて機能剤の効果が低い上に、接着剤により風合が硬化する欠点がある。
また、特開昭59−037956号公報や特開昭63−175117号公報によれば、低融点の合成繊維を含む繊維構造体を用いて、低融点繊維の溶融により銀抗菌剤粒子を固着するホットメルト固着方式も提案されているが、この技術は銀抗菌剤微粒子のブリーディングが多く、ブリーディングの本来機能は期待できるが、使用した低融点繊維の溶融により、隣接する繊維を融着固化して製品の風合が硬くなる欠点がある。
上述するように微粒子のブリーディングが適切で、柔軟な風合に加工できる微粒子の固着方法を熱望されているが、未だ知られていない。
In addition to the complexity of the manufacturing process, the conventional means for adhering to the fine particle fibers described above causes many of the antibacterial fine particles to remain inside the fiber by mixed spinning, and bleeding of the necessary antibacterial fine particles on the fiber surface is caused. Therefore, there is a problem that the antibacterial effect is hardly exhibited when the drug gradually exudes to the outside.
In the latter post-processing, a method of supporting the fiber product using an adhesive is generally used, and typically, there is a technique disclosed in Japanese Patent Laid-Open No. 02-021916. However, this technique has the disadvantages that fine particles are embedded in an adhesive and the effect of the functional agent is low, and the texture is cured by the adhesive.
Further, according to Japanese Patent Application Laid-Open Nos. 59-037956 and 63-175117, silver antibacterial agent particles are fixed by melting low-melting fibers using a fiber structure containing low-melting synthetic fibers. A hot melt fixing method has also been proposed, but this technique has many bleeding of silver antibacterial agent fine particles, and the original function of bleeding can be expected, but the adjacent fibers are fused and solidified by melting the low melting point fibers used. There is a drawback that the texture of the product becomes hard.
As described above, there is a keen desire for a fine particle fixing method that is suitable for fine particle bleeding and can be processed into a soft texture, but is not yet known.
上述する従来技術の適用では、微粒子、特に銀抗菌剤、防カビ剤、美白剤、皮膚保湿剤等の機能を有する微粒子や薬剤を繊維表面に微粒子を固着する場合に、耐久性を得ようとするほど、微粒子が接着剤に包み込まれて微粒子が繊維の表面からの突出せず、機能性粒子の本来機能が発揮されなくなる。
例えば銀系抗菌剤の例で言えば、接着剤に銀抗菌剤の微粒子が包み込まれると、抗菌の機能性の効果は得られなくなるが、銀抗菌剤微粒子を使用している目的は、本来有している機能を活用することで、そのためには銀抗菌剤の微粒子の一部が外側に突出することにより抗菌効果を発揮させることが必要である。
ところが、低融点繊維を使用してのホットメルトによる固着は、低融点繊維の溶融により隣接する繊維を融着することになり、微粒子の本来の効果はあっても、低融点の繊維を使用しているので、繊維フィラメントの熱融着に接点が多くなり、得られた繊維製品は必然的に風合いが悪く、硬くなる欠点があった。
そこで、従来の願望とする、微粒子による本来の突出効果は維持しつつ、柔軟な風合いの繊維製品とする繊維素材の製造法を現実化することを課題とするものものである。
In the application of the above-described prior art, it is intended to obtain durability when fine particles, particularly fine particles having a function such as silver antibacterial agent, antifungal agent, whitening agent, skin moisturizer, or the like are fixed to the fiber surface. Thus, the fine particles are encapsulated in the adhesive, and the fine particles do not protrude from the surface of the fiber, so that the original function of the functional particles is not exhibited.
For example, in the case of silver antibacterial agents, if silver antibacterial agent particles are encapsulated in the adhesive, the effect of antibacterial functionality will not be obtained, but the purpose of using silver antibacterial agent particles is inherently unique. For this purpose, it is necessary to exert antibacterial effects by projecting some of the fine particles of the silver antibacterial agent outward.
However, sticking by hot melt using low melting point fibers results in fusion of adjacent fibers by melting of low melting point fibers, and even though there is the original effect of fine particles, low melting point fibers are used. Therefore, the number of contacts is increased in the thermal fusion of the fiber filaments, and the obtained fiber product has a drawback that the texture is inevitably poor and hard.
Accordingly, it is an object of the present invention to realize a manufacturing method of a fiber material that is a fiber product having a soft texture while maintaining the original protruding effect by fine particles, which is a conventional desire.
本発明では、繊維素材を柔軟に加工するために、原料素材として湿熱接着性繊維を平行に配列されたスライバーを用いて、該スライバーが熱水処理による熱収縮によりクリンプを形成し、繊維間に空隙を発生することによって繊維素材は柔軟性を発揮することとなり、さらに繊維素材の表面には微粒子の一部が湿熱接着して固着することとなるので、微粒子の一部が外部に突出して微粒子の本来機能は発揮しつつ、得られた繊維素材は風合いよく、柔軟にすることができる。
本発明では、スキン及びコアの2部分よりなる湿熱接着性繊維のスレイバーを用いることによって可能としたもので、繊維のスキン部がエチレンビニールアルコール共重合体、コア部がポリエステルから形成されているので、熱水処理によっても繊維表面に接着性を有するが繊維全体が溶けることはない。
In the present invention, in order to process the fiber material flexibly, using a sliver in which wet and heat adhesive fibers are arranged in parallel as a raw material, the sliver forms a crimp by thermal contraction by hydrothermal treatment, By generating voids, the fiber material will exhibit flexibility, and furthermore, a part of the fine particles will adhere to the surface of the fiber material by wet heat bonding, so a part of the fine particles protrude to the outside and become fine particles. The fiber material obtained can be made soft and flexible while exhibiting its original function.
In the present invention, it is made possible by using a sliver of wet heat adhesive fibers consisting of two parts, a skin and a core, and the skin part of the fiber is made of an ethylene vinyl alcohol copolymer and the core part is made of polyester. Even with hot water treatment, the fiber surface has adhesiveness, but the entire fiber is not melted.
すなわち、本発明は上記課題を解決するために次の構成を特徴とする。That is, the present invention is characterized by the following configuration in order to solve the above problems.
請求項1に係る発明の繊維表面に多くの機能性微粒子の突起が突出した柔軟性繊維素材の製造方法は、機能性微粒子の分散液に、湿熱接着性繊維を平行に配列されたスライバーを含有する繊維素材からなる繊維製品を浸漬・絞液・乾燥して、該繊維素材に上記機能性微粒子を仮固定し、熱水処理を行い、該熱水処理による該繊維素材のクリンプ収縮によって該繊維素材間に空隙を生じるとともに、該繊維素材の表面に上記機能性微粒子の少なくとも一部が湿熱接着することを特徴とする。The method for producing a flexible fiber material in which protrusions of many functional fine particles protrude from the fiber surface of the invention according to claim 1 includes a sliver in which wet heat adhesive fibers are arranged in parallel in a dispersion of functional fine particles. A fiber product made of a fiber material is immersed, drawn and dried, the functional fine particles are temporarily fixed to the fiber material, subjected to hot water treatment, and the fiber material is crimped by the hot water treatment to cause the fiber to shrink. A void is formed between the materials, and at least a part of the functional fine particles is wet-heat bonded to the surface of the fiber material.
請求項2に係る発明の繊維表面に多くの機能性微粒子の突起が突出した柔軟性繊維素材の製造方法は、上記湿熱接着性繊維が、スキン及びコアの2部分より形成されてなり、スキン部がエチレンビニールアルコール共重合体、コア部がポリエステルであることを特徴とする。According to a second aspect of the present invention, there is provided a method for producing a flexible fiber material in which protrusions of many functional fine particles protrude from a fiber surface, wherein the wet heat adhesive fiber is formed of two parts, a skin and a core. Is an ethylene vinyl alcohol copolymer, and the core is polyester.
請求項3に係る発明の繊維表面に多くの機能性微粒子の突起が突出した柔軟性繊維素材の製造方法は、上記機能性微粒子が、銀系抗菌剤微粒子、ジンクピリチオン微粒子、化粧料微粒子、皮膚に機能性を付与する薬剤のマイクロカプセル微粒子又は石英斑岩微粒子より選ばれたものであることを特徴とする。According to a third aspect of the present invention, there is provided a method for producing a flexible fiber material in which protrusions of a large number of functional fine particles protrude from the fiber surface, wherein the functional fine particles are silver antibacterial agent fine particles, zinc pyrithione fine particles, cosmetic fine particles, and skin. It is characterized by being selected from microcapsule fine particles or quartz porphyry fine particles of a drug imparting functionality.
請求項4に係る発明の繊維製品は、請求項1〜3のいずれかに記載の方法により得られた繊維素材より形成されたことを特徴とする。The textile product of the invention according to claim 4 is formed from a fiber material obtained by the method according to any one of claims 1 to 3.
請求項5に係る発明の繊維製品は、不織布、織物、ニット、パイル織物又はパイルニットより選ばれることを特徴とする。 The fiber product of the invention according to claim 5 is selected from a nonwoven fabric, a woven fabric, a knit, a pile woven fabric, or a pile knit.
本発明で使用する湿熱接着性繊維素材としては、「ソフィスタ」(株式会社クラレ製品)を代表的なものとして用いるが、本発明では、特にこれらの繊維の有する、熱水の存在によって繊維表面への接着性を有する物性が活用可能なものである。
このような湿熱接着性繊維は、スキン部がエチレンビニールアルコール共重合体で、コア部がポリエステルよりなっており、織物やニットの製造原料として多用されているが、本発明では、単糸繊度2Dtexの500Dtexと250Dtexのスライバー、特にスライバー100%又は他の繊維と混用してスライバーとして用いるので、収束が少ないざっくりした組織のスライバーが好ましい。
本発明では、スライバーパイルニットでは海綿状の構造に抗菌性を付与した柔軟なボディ用スポンジを作成し、濡らして陰干しによって臭いの発生しない製品を得ることができる。
As a wet heat adhesive fiber material used in the present invention, “Sofista” (Kuraray Co., Ltd.) is used as a representative material. In the present invention, the surface of the fiber is brought into particular due to the presence of hot water of these fibers. The physical properties having the adhesive property can be utilized.
Such wet heat adhesive fibers have a skin part made of an ethylene vinyl alcohol copolymer and a core part made of polyester, and are often used as a raw material for producing woven fabrics and knits. In the present invention, the single yarn fineness is 2Dtex. 500Dtex and 250Dtex sliver, especially 100% sliver or mixed with other fibers and used as a sliver, a sliver having a rough texture with little convergence is preferred.
In the present invention, a sliver pile knit can produce a sponge for a flexible body that imparts antibacterial properties to a spongy structure and wets it to obtain a product that does not generate odor by drying in the shade.
本発明において、このような湿熱接着性繊維の表面に5μm以下の微粒子を付与して仮固定するには、該微粒子の分散液に湿熱接着性繊維製品を浸漬・絞液・乾燥する工程が必要であるが、上述する微粒子の仮固定は、接着剤を使用する必要はなく、分散安定剤として、公知の増粘剤の澱粉、マンナン、微生物産生グルカン、PVA等の使用が可能である。
また、本発明における熱水処理は、90℃以上で20〜30分で行うか、マイクロ波を用いて短時間に熱水処理を行うことのいずれもが可能である。
繊維素材として、単に湿熱接着性繊維を用いただけでは、繊維が収束した状態で湯水処理を行うと、繊維間の接着により硬化することとなるので、湿熱接着性繊維を平行に配列されたスライバーにより湯水処理により繊維間に空隙を発生させて柔軟性を得ることが可能となる。
In the present invention, in order to apply and temporarily fix fine particles of 5 μm or less to the surface of such wet heat-adhesive fibers, a step of immersing, drawing, and drying the wet heat-adhesive fiber product in the fine particle dispersion is required. However, the above-described temporary fixing of the fine particles does not require the use of an adhesive, and known thickeners such as starch, mannan, microbially produced glucan, and PVA can be used as the dispersion stabilizer.
In addition, the hot water treatment in the present invention can be performed at 90 ° C. or more for 20 to 30 minutes, or can be performed in a short time using a microwave.
If only wet heat-adhesive fibers are used as the fiber material, if hot water treatment is performed with the fibers converged, they will be cured by adhesion between the fibers, so the wet heat-adhesive fibers are aligned by a sliver arranged in parallel. It is possible to obtain flexibility by generating voids between the fibers by the hot water treatment.
本発明の繊維素材への微粒子の固着状態を図面で示すと、図1は、その概念図で、1は繊維、2は銀系抗菌剤微粒子のような微粒子、3は繊維同士の熱固着による接触交点、4は繊維間の空間であり、本発明では、熱融着交点が少ないので、柔軟性があり、風合いが優れている。 FIG. 1 is a conceptual diagram showing the state of adhesion of fine particles to the fiber material of the present invention. In FIG. 1, 1 is a fiber, 2 is a fine particle such as a silver-based antibacterial agent fine particle, and 3 is due to thermal fixation between fibers. The contact intersection 4 is a space between the fibers. In the present invention, since there are few heat fusion intersections, there is flexibility, and the texture is excellent.
本発明で使用する微粒子は、銀系抗菌剤微粒子、ジンクピリチオン微粒子、化粧料微粒子、皮膚に機能性を付与する薬剤のマイクロカプセル微粒子又は石英斑岩微粒子等の微粒子で、5μm以下の大きさがよく、5μm以上の大きさの微粒子では、湿熱接着繊維の太さ2Dtexに対して固着するには好ましくない。
銀系抗菌剤微粒子としては、銀ゼオライトにはゼオミック(シナネンゼオミック株式会社製品)があり、銀ガラスにはミリオンキラー(興亜硝子株式会社製品)があり、銀燐酸ジルコニウムにはノバロン(東亜合成株式会社製品)がある。
ジンクピリチオン(ZPT)のように水に不溶性の微粒子を、固着して防カビ効果を得ることができる。
皮膚に美白効果や保湿効果やスキンケア効果を有する薬剤を含有するマイキロカプセル微粒子としては、ビタミン、抗酸化剤、保湿剤等を含有するマイクロカプセル微粒子があり、サイクロデキストリンによる包接された微粒子を用いることもできる。
石英斑岩微粒子は、遠赤外線効果とK−40の効果があり、衣類に用いて湿熱効果や結構改善を得ることができる。
The fine particles used in the present invention are fine particles such as silver antibacterial agent fine particles, zinc pyrithione fine particles, cosmetic fine particles, microcapsule fine particles or quartz porphyry fine particles of a drug imparting functionality to the skin, and have a size of 5 μm or less. In the case of fine particles having a size of 5 μm or more, it is not preferable for fixing to the thickness 2Dtex of the wet heat bonding fiber.
As silver-based antibacterial particles, silver zeolite has Zeomic (product of Sinanen Zeomic Co., Ltd.), silver glass has Million Killer (product of Koa Glass Co., Ltd.), and silver zirconium phosphate has Novalon (Toa Gosei Co., Ltd.). Product).
Water-insoluble fine particles such as zinc pyrithione (ZPT) can be fixed to obtain an antifungal effect.
Microcapsule microparticles containing drugs that have whitening, moisturizing and skin care effects on the skin include microcapsule microparticles containing vitamins, antioxidants, moisturizers, etc. It can also be used.
Quartz porphyry fine particles have a far-infrared effect and an effect of K-40, and can be used for clothing to obtain a wet heat effect and a substantial improvement.
本発明は、繊維製品に対して機能性微粒子を固着するのに、多年の願望であった、繊維表面に多くの微粒子の突起が突出し、該微粒子の本来機能、例えば抗菌剤、美白剤、保湿剤、抗酸化剤等の多くの作用効果を十分に発揮でき、しかも風合いよい、柔軟な加工に仕上げることが可能である。ボディ用スポンジ、肌着、病院用寝衣、サポーター、等の肌に接する繊維製品では肌になじむ柔軟性が得られるのが本発明の効果である。 The present invention has been a long-standing desire for fixing functional fine particles to textile products, and many fine particle protrusions protrude from the fiber surface, and the original functions of the fine particles, such as antibacterial agents, whitening agents, moisturizing agents, etc. It is possible to achieve a flexible process that can sufficiently exhibit many functions and effects such as an agent, an antioxidant, and the like. It is an effect of the present invention that a textile product in contact with the skin such as a body sponge, an underwear, a hospital nightcloth, a supporter, and the like can be flexible to the skin.
(実施例1〜3)
湿熱接着性繊維の単糸繊度2Dtex250Dtexのスライバーを横糸として、縦糸にポリエステル糸80Dtex/40fを用いたガーゼ生地を用いる。
一方、PVA2重量%を溶解した水溶液に機能性微粒子を1重量%分散して分散液を調製しておく。
機能性微粒子の種類を変え、実施例1では銀ゼオライトとしてゼオミック(粒子径5μm)、実施例2では銀ガラスとしてミリオンキラー(粒径3μm)、実施例3ではジンクピリチオン(粒径2μm)をそれぞれ用いる。
上記調製した分散液に、上記機能性微粒子を各1重量%を分散した分散液に、浸漬し、絞液して、70℃で乾燥してガーゼ生地に銀抗菌剤微粒子を仮定着した。
次いで、得られた銀抗菌剤微粒子を仮定着したガーゼ生地を95℃に加熱した熱水に入れて20分間熱水処理をして乾燥した。
乾燥後に柔軟で抗菌効果を有する生地を得ることができた。
抗菌効果は表1に示す通りであった。
表中の「0hr」は植菌した初期の菌数であり、「12hr」は、12時間後の菌数を「抗菌効果」として示した。また、機能性微粒子として抗菌剤による効果を実施例に示したのは、微粒子のブリーディングの良否を抗菌効果により具体的に数値表現できるからである。
なお、比較例として抗菌剤を固着しないブランクの微生物に対する影響を示すと、大腸菌では1.0×104の植菌数(0hr)が12時間後には3.2×1012に増殖がされ、黄色ブドウ球菌では1.3×104の植菌数(0hr)が12時間後には2.5×1013に増殖がされる。このことから抗菌剤を固着しない場合、微生物が増殖し、汚染に対して弱いものであることがわかった。
(Examples 1-3)
A gauze fabric using a sliver having a single yarn fineness of 2Dtex250Dtex of wet heat adhesive fiber as weft and polyester yarn 80Dtex / 40f as warp is used.
Meanwhile, a dispersion is prepared by dispersing 1% by weight of functional fine particles in an aqueous solution in which 2% by weight of PVA is dissolved.
In Example 1, zeomic (particle diameter 5 μm) is used as silver zeolite in Example 1, million killer (particle diameter 3 μm) is used as silver glass in Example 2, and zinc pyrithione (particle diameter 2 μm) is used in Example 3. .
In the dispersion prepared above, the functional fine particles were immersed in a dispersion in which 1% by weight of each was dispersed, squeezed, dried at 70 ° C., and silver antibacterial fine particles were assumed on the gauze fabric.
Next, the gauze dough on which the obtained silver antibacterial agent fine particles were assumed was put in hot water heated to 95 ° C., treated with hot water for 20 minutes and dried.
After drying, a soft and antibacterial fabric could be obtained.
The antibacterial effect was as shown in Table 1.
“0hr” in the table is the initial number of inoculated bacteria, and “12hr” indicates the number of bacteria after 12 hours as “antibacterial effect”. Moreover, the reason why the effect of the antibacterial agent as the functional fine particles is shown in the examples is that the quality of the bleeding of the fine particles can be expressed specifically by the antibacterial effect.
In addition, when the influence with respect to the blank microorganisms which do not adhere an antibacterial agent as a comparative example is shown, in E. coli, the inoculation number of 1.0 × 10 4 (0 hr) is increased to 3.2 × 10 12 after 12 hours, In S. aureus, the number of inoculations of 1.3 × 10 4 (0 hr) is increased to 2.5 × 10 13 after 12 hours. From this, it was found that when the antibacterial agent is not fixed, the microorganisms grow and are vulnerable to contamination.
1 繊維
2 微粒子
3 接触交点
4 空間
1 Fiber 2 Fine particle 3 Contact intersection 4 Space
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