JP4777892B2 - Flame retardant synthetic fiber, flame retardant fiber composite and upholstered furniture product using the same - Google Patents
Flame retardant synthetic fiber, flame retardant fiber composite and upholstered furniture product using the same Download PDFInfo
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- JP4777892B2 JP4777892B2 JP2006529172A JP2006529172A JP4777892B2 JP 4777892 B2 JP4777892 B2 JP 4777892B2 JP 2006529172 A JP2006529172 A JP 2006529172A JP 2006529172 A JP2006529172 A JP 2006529172A JP 4777892 B2 JP4777892 B2 JP 4777892B2
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING 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
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-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
- D04H1/42—Non-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
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/07—Addition of substances to the spinning solution or to the melt for making fire- or flame-proof filaments
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/48—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of halogenated hydrocarbons
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- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Artificial Filaments (AREA)
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Description
本発明は、燃焼時に極めて高い炭化性と自己消火性を発現することで、寝具や家具等に用いられる高度な難燃性を必要とする繊維製品に好適に使用できる高度な難燃性を有する難燃性合成繊維および該難燃性合成繊維を含む難燃繊維複合体およびそれを用いた布張り家具製品に関する。 The present invention exhibits high flame retardancy that can be suitably used for textiles that require high flame retardancy, such as bedding and furniture, by exhibiting extremely high carbonization and self-extinguishing properties during combustion. The present invention relates to a flame retardant synthetic fiber, a flame retardant fiber composite containing the flame retardant synthetic fiber, and a upholstered furniture product using the same.
近年、衣食住の安全性確保の要求が強まり、防炎の観点より難燃素材の必要性が高まってきている。そのような中で、特に発生時に人的被害が大きい就寝中の火災を防止するため、寝具や家具等に使用される素材への難燃性付与の必要性が高まってきている。 In recent years, demands for ensuring the safety of clothing, food and housing have increased, and the need for flame retardant materials has increased from the viewpoint of flameproofing. Under such circumstances, in order to prevent a fire during sleeping, which causes great human damage at the time of occurrence, there is an increasing need for imparting flame retardancy to materials used for bedding and furniture.
これら寝具や家具等の製品においては、使用時の快適さや意匠性のために綿やポリエステル、ウレタンフォームなどの易燃性素材がその内部や表面に用いられる事が多い。それら製品の防炎性の確保には、適当な難燃素材をこれら製品中に使用することで、その易燃性素材への着炎を長時間にわたり防止する高度な難燃性を具備することが重要である。また、その難燃素材は、これら寝具や家具等の製品の快適さや意匠性を損なわないものでなければならない。 In products such as bedding and furniture, flammable materials such as cotton, polyester, and urethane foam are often used on the inside and the surface for comfort and design at the time of use. In order to ensure the flame resistance of these products, by using appropriate flame retardant materials in these products, the products must have high flame retardant properties that prevent flames from flammable materials for a long time. is important. In addition, the flame retardant material must not impair the comfort and design of products such as bedding and furniture.
この難燃素材に使用される繊維製品に対し、過去様々な難燃性合成繊維や防炎薬剤が検討されてきたが、この高度な難燃性と寝具や家具等の製品に求められる快適さや意匠性といった要件を充分に兼ね合わせたものは未だ現れていない。 Various flame retardant synthetic fibers and flame retardants have been studied in the past for the fiber products used in this flame retardant material. The high flame retardancy and comfort required for products such as bedding and furniture There has not yet been a product that fully combines requirements such as design.
例えば、綿布に防炎薬剤を塗布する、いわゆる後加工防炎という手法があるが、防炎薬剤の付着量のばらつき、付着による布の硬化、洗濯による脱離、人体への安全性などの問題があった。 For example, there is a so-called post-processing flame-proofing method that applies a flameproofing agent to cotton cloth, but there are problems such as variations in the amount of flameproofing agent attached, hardening of the cloth due to adhesion, detachment due to washing, safety to the human body, etc. was there.
また、安価な素材であるポリエステルを用いた場合には、ポリエステルは炭化成分となりえないため、強制燃焼させた場合には溶融し穴が空き、構造を維持することが出来ず、前述の寝具や家具等に用いられる綿やウレタンフォームへ着炎してしまい、性能としては全く不充分であった。 In addition, when polyester, which is an inexpensive material, is used, polyester cannot become a carbonizing component, so when forcedly burned, it melts and has holes, and the structure cannot be maintained. The cotton and urethane foam used for furniture and the like were flared, and the performance was quite inadequate.
また、アラミド繊維やノボロイド繊維のような有機耐熱性繊維からなる布は、難燃性は優れているが極めて高価であり、さらに開繊時の加工性の問題や、吸湿性や触感の悪さ、そして染色性の低さから意匠性の高い色柄を得るのが難しいという問題もある。 In addition, fabrics made of organic heat-resistant fibers such as aramid fibers and novoloid fibers are excellent in flame retardancy, but are extremely expensive.Furthermore, there are problems with workability at the time of opening, hygroscopicity and poor touch, There is also a problem that it is difficult to obtain a design with high design properties due to low dyeability.
これらの家具、寝具に使用される難燃繊維素材の欠点を改良し、一般的な特性として要求される優れた風合、吸湿性、触感を有し、かつ、安定した難燃性を有する素材として、難燃剤を大量に添加して高度に難燃化した含ハロゲン繊維と、難燃化していない他の繊維とを組み合わせた難燃繊維複合体(特許文献1)が、提案されている。また、耐熱性繊維を少量混ぜることで、作業服用途に使用可能な、高度難燃繊維複合体(特許文献2)で、風合いや吸湿性に優れ、高度な難燃性を有するとの記載はあるが、有機耐熱繊維は一般に着色し布帛の白度が不十分であり、また染色による発色にも問題があり、製品の意匠性に問題のある難燃繊維複合体であった。更に、これらはまた、本質的に難燃性である繊維と含ハロゲン繊維から嵩高さを有する難燃性不織布(特許文献3)が提案されているが、これらの方法では複数の繊維を複合化して用いなければ高度な難燃性が得られず、製品の製造工程が複雑になり、また、有機耐熱繊維や本質的に難燃性である繊維は一般的に高価でありコスト的に不利であるという問題点があった。またガラス成分により難燃化した難燃ポリエステル素材もあるが、ガラス成分量が著しく多いためコスト高や繊維化時の工程安定性に問題があり繊維化には至っていない。(特許文献4)
本発明は、従来の難燃性合成繊維では解決が困難であった課題、すなわち、加工性や風合い、触感が良好で、意匠性のある家具、寝具等に使用されうる難燃性合成繊維、難燃性複合体およびそれを用いた布張り家具製品を容易にかつ安価に提供することを目的とする。 The present invention is a problem that has been difficult to solve with conventional flame-retardant synthetic fibers, i.e., processability, texture, and tactile feel, flame-retardant synthetic fibers that can be used for furniture, bedding, and the like, An object of the present invention is to easily and inexpensively provide a flame retardant composite and a upholstered furniture product using the same.
本発明者らは、前記問題を解決するため鋭意検討を重ねた結果、ハロゲン原子を含有する合成繊維にガラス成分とアンチモン化合物を併用含有させることで、難燃性を保持したまま、加工性や風合い・触感にマイナス影響を与えるガラス成分の減量が可能となることを見出した。このように燃焼時に極めて高い炭化性と自己消火性を発現することで、燃焼後の繊維形態を維持する高度な難燃性を兼ね備えた難燃性合成繊維が得ることができた。 As a result of intensive studies to solve the above-mentioned problems, the present inventors have incorporated a glass component and an antimony compound in combination with a synthetic fiber containing a halogen atom. We have found that it is possible to reduce the amount of glass components that negatively affect the texture and feel. Thus, by exhibiting extremely high carbonization and self-extinguishing properties at the time of combustion, it was possible to obtain a flame-retardant synthetic fiber having high flame retardancy that maintains the fiber form after combustion.
この結果、難燃素材の意匠性を損なうことなく、かつ長時間の炎にも耐え得る難燃性や自己消火性を兼ね備えた家具、寝具等に用いられる繊維製品を得ることが可能な難燃性合成繊維が安価に得られることを見出した。また、耐熱性繊維単独で使用するときの問題であった、加工性や価格の問題も改善できることを見出し、本発明の難燃性合成繊維、該難燃性繊維を含む難燃性複合体、およびそれを用いた布張り家具製品に到達した。 As a result, it is possible to obtain a textile product used for furniture, bedding, etc. that has flame retardancy and self-extinguishing properties that can withstand a long flame without impairing the design of the flame retardant material. The synthetic synthetic fiber was found to be obtained at low cost. In addition, it was found that the problem of processability and price, which was a problem when using a heat resistant fiber alone, can be improved, the flame retardant synthetic fiber of the present invention, a flame retardant composite containing the flame retardant fiber, And we have reached upholstered furniture products using it.
すなわち、本発明は、ハロゲン原子を17重量%以上含む100重量部に対し、ガラス成分とアンチモン化合物の合計を6〜50重量部含む繊維(A)10重量部以上と、天然繊維および/または化学繊維のうち少なくとも1種の繊維(B)90重量部以下からなる難燃性合成繊維及び難燃繊維複合体、およびこれを用いた布張り家具製品であって、前記ガラス成分とアンチモン化合物剤の合計中、ガラス成分が5〜49重量部、アンチモン化合物が1〜45重量部であり、好ましくは前記ハロゲン原子を17重量%以上含む重合体が、アクリロニトリル30〜70重量部、ハロゲン含有ビニルおよび/またはハロゲン含有ビニリデン単量体70〜30重量部、およびこれらと共重合可能なビニル系単量体0〜10重量部からなる難燃性合成繊維及び燃繊維複合体、およびこれを用いた布張り家具製品に関する。また前記天然繊維および/または化学繊維のうち少なくとも1種の繊維(B)にポリエステル系繊維を40重量部以下含み、前記難燃繊維複合体が不織布、特には炎遮蔽バリア用不織布であり、前記繊維(B)であるポリエステル系繊維が低融点バインダー繊維である繊維複合体およびこれを用いた布張り家具製品に関する。 That is, in the present invention, 10 parts by weight or more of the fiber (A) containing 6 to 50 parts by weight of the total of the glass component and the antimony compound, 100 parts by weight of halogen atoms and 17 parts by weight or more, natural fibers and / or chemicals. A flame-retardant synthetic fiber and a flame-retardant fiber composite composed of 90 parts by weight or less of at least one kind of fiber (B), and a upholstered furniture product using the same, comprising the glass component and the antimony compound agent In the total, the glass component is 5 to 49 parts by weight, the antimony compound is 1 to 45 parts by weight, and the polymer containing 17% by weight or more of the halogen atom is preferably 30 to 70 parts by weight of acrylonitrile, halogen-containing vinyl and / or Or a flame retardant synthesis comprising 70 to 30 parts by weight of a halogen-containing vinylidene monomer and 0 to 10 parts by weight of a vinyl monomer copolymerizable therewith Wei and retardant fiber composite, and to upholstered furniture products using the same. Further, at least one of the natural fibers and / or chemical fibers (B) contains 40 parts by weight or less of a polyester fiber, and the flame retardant fiber composite is a nonwoven fabric, particularly a nonwoven fabric for a flame shielding barrier, The present invention relates to a fiber composite in which a polyester fiber which is a fiber (B) is a low-melting-point binder fiber, and a upholstered furniture product using the same.
さらに具体的に本発明を説明すると、ハロゲン原子を17重量%以上含む重合体100重量部に対し、ガラス成分とアンチモン化合物を合計6〜50重量部含む難燃性合成繊維である。好ましくは、前記ガラス成分のガラス転移温度が200〜700℃であり、ガラス成分を5〜49重量部を前記アンチモン化合物を1〜45重量部含有し、前記ハロゲ原子含む重合体のハロゲン含量が、20〜86%であり、更に好ましくは前記ハロゲン原子を17重量%以上含む重合体が、アクリロニトリル30〜70重量部、ハロゲン含有ビニルおよび/またはハロゲン含有ビニリデン単量体70〜30重量部、およびこれらと共重合可能なビニル系単量体0〜10重量部からなる難燃性合成繊維(A)に関する。 More specifically, the present invention is a flame-retardant synthetic fiber containing a total of 6 to 50 parts by weight of a glass component and an antimony compound with respect to 100 parts by weight of a polymer containing 17% by weight or more of a halogen atom. Preferably, the glass transition temperature of the glass component is 200 to 700 ° C., the glass component is contained in an amount of 5 to 49 parts by weight, the antimony compound is contained in an amount of 1 to 45 parts by weight, and the halogen content of the halogen atom-containing polymer is 20 to 86%, and more preferably the polymer containing 17% by weight or more of the halogen atom is 30 to 70 parts by weight of acrylonitrile, 70 to 30 parts by weight of halogen-containing vinyl and / or halogen-containing vinylidene monomer, and these It is related with a flame-retardant synthetic fiber (A) which consists of 0-10 weight part of vinyl-type monomers copolymerizable with.
また前記天然繊維および/または化学繊維のうち少なくとも1種の繊維(B)にポリエステル系繊維を40重量部以下含み、前記難燃繊維複合体が不織布、特には炎遮蔽バリア用不織布であり、前記繊維(B)であるポリエステル系繊維が低融点バインダー繊維である繊維複合体およびこれを用いた布張り家具製品に関する。 Further, at least one of the natural fibers and / or chemical fibers (B) contains 40 parts by weight or less of a polyester fiber, and the flame retardant fiber composite is a nonwoven fabric, particularly a nonwoven fabric for a flame shielding barrier, The present invention relates to a fiber composite in which a polyester fiber which is a fiber (B) is a low-melting-point binder fiber, and a upholstered furniture product using the same.
本発明の難燃性合成繊維は、風合い、触感、視感などの意匠性や、加工性に優れ、長時間の炎にも耐え得る高度な難燃性や自己消火性を有する繊維製品を得ることを可能とするものである。また本発明の難燃複合体およびこれを使用したインテリア繊維製品は、風合い、触感、視感などの意匠性や、加工性に優れ、長時間の炎にも繊維形態を維持することで高度な難燃性を有することを可能とするものである。 The flame-retardant synthetic fiber of the present invention provides a fiber product having high flame retardancy and self-extinguishing properties that are excellent in design properties such as texture, touch, and visual feel, and processability, and can withstand a long flame. It is possible to do that. In addition, the flame-retardant composite of the present invention and interior fiber products using the same are excellent in design properties such as texture, touch, and visual sense, and processability, and are highly advanced by maintaining the fiber form even for a long flame. It is possible to have flame retardancy.
本発明のハロゲン原子を17%以上含む重合体における好ましいハロゲン含量の下限としては20%、さらには26%、上限としては86%、さらには73%、とくには48%である。前記ハロゲン含有量が17%未満の場合、繊維を難燃化することが困難になり、好ましくない。ハロゲン含有量の上限が86%であるのは、臭化ビニリデン単独重合体のハロゲン含有量であり、この値がハロゲン含有量の上限値となる。これ以上のハロゲン含有量を得るためにはさらにモノマー中のハロゲン原子を増やす必要があり、技術的に現実的ではなくなる。 The lower limit of the preferable halogen content in the polymer containing 17% or more of the halogen atom of the present invention is 20%, further 26%, the upper limit is 86%, further 73%, especially 48%. When the halogen content is less than 17%, it is difficult to make the fiber flame-retardant, which is not preferable. The upper limit of the halogen content is 86% is the halogen content of the vinylidene bromide homopolymer, and this value is the upper limit of the halogen content. In order to obtain a higher halogen content, it is necessary to increase the number of halogen atoms in the monomer, which is not technically practical.
前記のごときハロゲン原子を17%以上含む重合体としては、たとえばハロゲン原子を含有する単量体の重合体、前記ハロゲン原子を含有する単量体とハロゲン原子を含有しない単量体との共重合体、ハロゲン原子を含有する重合体とハロゲン原子を含有しない重合体とを混合したもの、ハロゲン原子を含有しない単量体もしくは重合体を重合中〜重合後に、ハロゲン原子を導入したハロゲン原子含有重合体などがあげられるが、これらに限定されるものではない。 Examples of the polymer containing a halogen atom of 17% or more include, for example, a polymer of a monomer containing a halogen atom, and a copolymer of a monomer containing a halogen atom and a monomer not containing a halogen atom. A mixture of a polymer containing a halogen atom and a polymer not containing a halogen atom, a monomer or polymer containing no halogen atom during polymerization, and after polymerization, Examples include, but are not limited to, coalescence.
このようなハロゲン原子を17重量%以上含む重合体の具体例としては、たとえば塩化ビニル、塩化ビニリデン、臭化ビニル、臭化ビニリデン、フッ化ビニル、フッ化ビニリデンなどのハロゲン含有ビニル系またはビニリデン系単量体の単独重合体または2種以上の共重合体;アクリロニトリル−塩化ビニル、アクリロニトリル−塩化ビニリデン、アクリロニトリル−臭化ビニル、アクリロニトリル−フッ化ビニル、アクリロニトリル−塩化ビニル−塩化ビニリデン、アクリロニトリル−塩化ビニル−臭化ビニル、アクリロニトリル−塩化ビニリデン−臭化ビニル、アクリロニトリル−塩化ビニリデン−フッ化ビニリデンなどのハロゲン含有ビニル系またはビニリデン系単量体とアクリロニトリルとの共重合体;塩化ビニル、塩化ビニリデン、臭化ビニル、臭化ビニリデン、フッ化ビニル、フッ化ビニリデンなどのハロゲン含有ビニル系またはビニリデン系単量体の1種以上とアクリロニトリルおよびこれらと共重合可能なビニル系単量体との共重合体;アクリロニトリル単独重合体にハロゲン含有化合物を添加・重合させた重合体;ハロゲン含有ポリエステル;ビニルアルコールと塩化ビニルの共重合体;ポリエチレンやポリ塩化ビニルなどを塩素付加処理した重合体などがあげられるが、これらに限定されるものではない。また、前記単独重合体や共重合体を適宜混合して使用してもよい。 Specific examples of such a polymer containing 17% by weight or more of halogen atoms include halogen-containing vinyl-based or vinylidene-based polymers such as vinyl chloride, vinylidene chloride, vinyl bromide, vinylidene bromide, vinyl fluoride, vinylidene fluoride, and the like. Monomer homopolymer or two or more copolymers; acrylonitrile-vinyl chloride, acrylonitrile-vinylidene chloride, acrylonitrile-vinyl bromide, acrylonitrile-vinyl fluoride, acrylonitrile-vinyl chloride-vinylidene chloride, acrylonitrile-vinyl chloride -Copolymers of halogen-containing vinyl or vinylidene monomers such as vinyl bromide, acrylonitrile-vinylidene chloride-vinyl bromide, acrylonitrile-vinylidene chloride-vinylidene fluoride and acrylonitrile; vinyl chloride, vinylidene chloride Copolymers of one or more halogen-containing vinyl-based or vinylidene-based monomers such as vinyl bromide, vinylidene bromide, vinyl fluoride, and vinylidene fluoride with acrylonitrile and vinyl monomers copolymerizable therewith A polymer obtained by adding and polymerizing a halogen-containing compound to an acrylonitrile homopolymer; a halogen-containing polyester; a copolymer of vinyl alcohol and vinyl chloride; a polymer obtained by adding chlorine to polyethylene or polyvinyl chloride, and the like. However, it is not limited to these. Moreover, you may use the said homopolymer and copolymer suitably mixing.
前記ハロゲン原子を17重量%以上含む重合体が、アクリロニトリル30〜70重量部、ハロゲン含有ビニル系単量体70〜30重量部およびそれらと共重合可能なビニル系単量体0〜10重量部、好ましくはアクリロニトリル40〜60重量部、ハロゲン含有ビニル系単量体60〜40重量部およびそれらと共重合可能なビニル系単量体0〜10重量部からなる重合体の場合には、得られる繊維が所望の性能(強度、難燃性、染色性など)を有しつつアクリル繊維の風合を有するため特に好ましい。 The polymer containing 17% by weight or more of the halogen atom is 30 to 70 parts by weight of acrylonitrile, 70 to 30 parts by weight of a halogen-containing vinyl monomer and 0 to 10 parts by weight of a vinyl monomer copolymerizable therewith, Preferably, in the case of a polymer composed of 40 to 60 parts by weight of acrylonitrile, 60 to 40 parts by weight of a halogen-containing vinyl monomer and 0 to 10 parts by weight of a vinyl monomer copolymerizable therewith, the resulting fiber Is particularly preferable because it has a texture of acrylic fiber while having desired performance (strength, flame retardancy, dyeability, etc.).
前記それらと共重合可能なビニル系単量体としては、たとえばアクリル酸、そのエステル、メタクリル酸、そのエステル、アクリルアミド、メタクリルアミド、酢酸ビニル、ビニルスルホン酸、その塩、メタリルスルホン酸、その塩、スチレンスルホン酸、その塩、2−アクリルアミド−2−メチルスルホン酸、その塩などがあげられ、それらの1種または2種以上が用いられる。また、そのうち少なくとも1種がスルホン酸基含有ビニル系単量体の場合には、染色性が向上するため好ましい。 Examples of the vinyl monomers copolymerizable therewith include acrylic acid, its ester, methacrylic acid, its ester, acrylamide, methacrylamide, vinyl acetate, vinyl sulfonic acid, its salt, methallyl sulfonic acid, its salt Styrene sulfonic acid, a salt thereof, 2-acrylamido-2-methylsulfonic acid, a salt thereof, and the like, and one or more of them are used. In addition, it is preferable that at least one of them is a sulfonic acid group-containing vinyl monomer because dyeability is improved.
前記ハロゲン含有ビニル系単量体およびアクリロニトリルからの単位を含む共重合体の具体例としては、例えば塩化ビニル50部、アクリロニトリル49部、スチレンスルホン酸ソーダ1部よりなる共重合体、塩化ビニリデン47部、アクリロニトリル51.5部、スチレンスルホン酸ソーダ1.5部よりなる共重合体、塩化ビニリデン41部、アクリロニトリル56部、2−アクリルアミド−2−メチルスルホン酸ソーダ3部などがあげられる。これは、既知の重合方法で得る事が出来る。 Specific examples of the copolymer containing units from the halogen-containing vinyl monomer and acrylonitrile include, for example, a copolymer comprising 50 parts of vinyl chloride, 49 parts of acrylonitrile and 1 part of sodium styrenesulfonate, 47 parts of vinylidene chloride. And a copolymer comprising 51.5 parts of acrylonitrile and 1.5 parts of styrene sulfonic acid soda, 41 parts of vinylidene chloride, 56 parts of acrylonitrile, 3 parts of 2-acrylamido-2-methylsulfonic acid soda and the like. This can be obtained by known polymerization methods.
本発明に用いるガラス成分としては、200〜700℃にガラス転移温度を有するものでは何でも良く、例えばSiO2−PbO系、SiO2−PbO−ZnO系、
SiO2−B2O3−Na2O系、SiO2−B2O3−PbO系、SiO2−Al2O3系、
B2O3−PbO系、B2O3−ZnO系、B2O3−Na2O−PbO系、
B2O3−PbO−ZnO系、B2O3−P2O5系、B2O3−Bi2O3−ZnO系、
P2O5−ZnO系などをあげることができるがこれらに限定されるものではない。またこれらを組み合わせて使用しても何ら支障はない。その使用量は、ハロゲン原子を17%以上含む重合 体100重量部に対して5〜49重量部、好ましくは7〜40重量部、更に好ましくは10〜30重量部である。5重量部未満だと燃焼時に炭化層の形態保持効果が得られず求める難燃性を得る事が難しくなり、49重量部を超えると十分な形態保持効果は得られるが繊維化時の製造工程において糸切れなどが発生するため好ましくない。また、前記ガラス成分のガラス転移温度は200℃〜700℃、好ましくは250〜600℃である。200℃未満だと燃焼時のガラス成分の溶融が早いため、また700℃を超えると燃焼時にガラス成分が溶融しないため、何れも意図する炭化効果を得ることが出来ない。また、前記ガラス成分の平均粒子径としては、3μm以下であることがハロゲン含有重合体にガラス成分を添加してなる繊維の製造工程上におけるノズル詰りなどのトラブル回避、繊維の強度向上、繊維中でのガラス成分粒子の分散などの点から好ましい。更に前記ガラス成分は、ブロッキング性改善のために粒子表面に化学的修飾を施しても支障ない。The glass component used in the present invention, 200 to 700 ° C. may whatever those having a glass transition temperature, for example, SiO 2 -PbO-based, SiO 2 -PbO-ZnO-based,
SiO 2 —B 2 O 3 —Na 2 O system, SiO 2 —B 2 O 3 —PbO system, SiO 2 —Al 2 O 3 system,
B 2 O 3 —PbO system, B 2 O 3 —ZnO system, B 2 O 3 —Na 2 O—PbO system,
B 2 O 3 —PbO—ZnO system, B 2 O 3 —P 2 O 5 system, B 2 O 3 —Bi 2 O 3 —ZnO system,
Examples thereof include P 2 O 5 —ZnO, but are not limited thereto. Moreover, there is no problem even if these are used in combination. The amount used is 5 to 49 parts by weight, preferably 7 to 40 parts by weight, more preferably 10 to 30 parts by weight, based on 100 parts by weight of the polymer containing 17% or more of halogen atoms. If the amount is less than 5 parts by weight, it is difficult to obtain the required flame retardancy because the shape retention effect of the carbonized layer is not obtained during combustion, and if it exceeds 49 parts by weight, a sufficient shape retention effect can be obtained, but the manufacturing process at the time of fiberization In this case, thread breakage or the like occurs. Moreover, the glass transition temperature of the said glass component is 200 to 700 degreeC, Preferably it is 250 to 600 degreeC. If it is less than 200 ° C., the glass component melts quickly during combustion, and if it exceeds 700 ° C., the glass component does not melt during combustion, so that neither of the intended carbonization effects can be obtained. Further, the average particle size of the glass component is 3 μm or less, avoiding troubles such as nozzle clogging in the production process of the fiber obtained by adding the glass component to the halogen-containing polymer, improving the strength of the fiber, From the viewpoint of dispersion of the glass component particles in FIG. Further, the glass component can be chemically modified on the particle surface to improve the blocking property.
前記アンチモン化合物としては、三酸化アンチモン、四酸化アンチモン、五酸化アンチモンなどの酸化アンチモン化合物、アンチモン酸やその塩類、オキシ塩化アンチモンなどの無機アンチモン化合物などを挙げることができるがこれらに限定されるものではない。その量はハロゲン原子を17%以上含む重合体100重量部に対し1〜45重量部、好ましくは3〜35重量部、更に好ましくは5〜30重量部である。1重量部未満では自己消火効果が少ないため、意図するような十分な高度な難燃性を得ることが出来ないし、45重量部を超えるとその効果が飽和しコスト高の要因となるため好ましくない。 Examples of the antimony compounds include, but are not limited to, antimony oxide compounds such as antimony trioxide, antimony tetraoxide, and antimony pentoxide, inorganic antimony compounds such as antimonic acid and salts thereof, and antimony oxychloride. is not. The amount is 1 to 45 parts by weight, preferably 3 to 35 parts by weight, and more preferably 5 to 30 parts by weight with respect to 100 parts by weight of a polymer containing 17% or more of halogen atoms. If the amount is less than 1 part by weight, the self-extinguishing effect is small, so that a sufficiently high flame retardance as intended cannot be obtained. If the amount exceeds 45 parts by weight, the effect is saturated and the cost is increased, which is not preferable. .
本発明の難燃性合成繊維には、必要に応じて帯電防止剤、熱着色防止剤、耐光性向上剤、白度向上剤、失透性防止剤、着色剤、難燃剤といったその他添加剤を含有せしめても良い。例えば、難燃剤としては、ヘキサブロモベンゼン、ヘキサブロモシクロドデカン、塩化パラフィンなどのハロゲン化合物、トリス(2,3−ジクロロプロピル)ホスフェートなどの含ハロゲンリン化合物、ポリリン酸アンモニウム、ジブチルアミノホスフェートなどのP系化合物、酸化マグネシウム、水酸化マグネシウム、炭酸マグネシウム などのMg系化合物、酸化第2スズ、メタスズ酸、オキシハロゲン化第2スズ、水酸化第1スズ、4塩化スズ、ZnSnO3、ZnSn(OH)6などのSn系化合物、酸化亜鉛、硼酸亜鉛などのZn系化合物、酸化モリブデンなどのMo系化合物、酸化チタン、チタン酸バリウムなどのチタン系化合物、硫酸メラミン、スルファミン酸グアニジンなどのN系化合物、水酸化アルミニウムなどのアルミニウム系化合物、酸化ジルコニウムなどのジルコニウム系化合物、錫酸マグネシウム、錫酸ジルコニウム、錫酸亜鉛、ヒドロキシ錫酸亜鉛などのスズ化合物などが挙げられるがこれらに限定されるものではない。The flame retardant synthetic fiber of the present invention may contain other additives such as an antistatic agent, a thermal coloring inhibitor, a light resistance improver, a whiteness improver, a devitrification inhibitor, a colorant, and a flame retardant as necessary. It may be included. For example, flame retardants include halogen compounds such as hexabromobenzene, hexabromocyclododecane, chlorinated paraffin, halogen-containing phosphorus compounds such as tris (2,3-dichloropropyl) phosphate, ammonium polyphosphate, dibutylaminophosphate and the like. Compounds, Mg compounds such as magnesium oxide, magnesium hydroxide, magnesium carbonate, stannic oxide, metastannic acid, stannic oxyhalide, stannous hydroxide, tin tetrachloride, ZnSnO 3 , ZnSn (OH) Sn compounds such as 6 , Zn compounds such as zinc oxide and zinc borate, Mo compounds such as molybdenum oxide, titanium compounds such as titanium oxide and barium titanate, N compounds such as melamine sulfate and guanidine sulfamate, Aluminum such as aluminum hydroxide Um compounds, zirconium compounds such as zirconium oxide, stannate magnesium stannate, zirconium, zinc stannate, but such as tin compounds such as zinc hydroxystannate are exemplified but not limited thereto.
さらに本発明は、難燃繊維複合体によって布張りされた、マットレス等の寝具、椅子、ソファー、車両用座席等を提供できる。 Furthermore, the present invention can provide a bedding such as a mattress, a chair, a sofa, a vehicle seat, and the like, which are upholstered by a flame-retardant fiber composite.
マットレスとしては、例えば、金属製のコイルが内部に用いられたポケットコイルマットレス、ボックスコイルマットレス、あるいはスチレンやウレタン樹脂などを発泡させたインシュレーターが内部に使用されたマットレス等がある。本発明に使用される難燃繊維複合体による防炎性が発揮されることにより、前記マットレス内部の構造体への延焼が防止出来るため、何れの構造のマットレスおいても、難燃性と同時に優れた風合いや触感に優れたマットレスを得ることができる。 Examples of the mattress include a pocket coil mattress in which a metal coil is used, a box coil mattress, and a mattress in which an insulator in which styrene or urethane resin is foamed is used. By exhibiting flame retardancy due to the flame retardant fiber composite used in the present invention, it is possible to prevent the spread of fire to the structure inside the mattress. A mattress excellent in texture and touch can be obtained.
一方、椅子としては、屋内にて使用される、ストゥール、ベンチ、サイドチェア、アームチェア、ラウンジチェア・ソファー、シートユニット(セクショナルチェア、セパレートチェア)、ロッキングチェア、フォールディングチェア、スタッキングチェア、スィーブルチェア、あるいは屋外で車両用座席等に使用される、自動車シート、船舶用座席、航空機用座席、列車用座席などが挙げられるが、これらにおいても通常の家具として要求される外観や触感と同時に内部の延焼を防止する機能を有する布張り製品を得ることができる。 On the other hand, as chairs used indoors, tools, benches, side chairs, armchairs, lounge chairs and sofas, seat units (sectional chairs, separate chairs), rocking chairs, folding chairs, stacking chairs, swivel chairs, Or automobile seats, marine seats, aircraft seats, train seats, etc., used outdoors for vehicle seats, etc., but also in these, the internal fire spreads at the same time as the appearance and feel required for normal furniture It is possible to obtain a upholstered product having a function of preventing the above.
また、テンピュール(登録商標)素材(テンピュールワールド社製、Tempur World,Inc.)に代表される圧力分散機能を有する低反発ウレタンフォームを使用したマットレスや椅子においては通常のスチレンやウレタン樹脂を発泡させたフォーム材料を用いたマットレスや椅子に比べて極めて易燃性であるが、本発明に使用される難燃複合体による防炎性が発揮されることにより、マットレスや椅子の内部構造体である低反発ウレタンフォームへの延焼が防止出来る。 Also, in mattresses and chairs using low-resilience urethane foam having a pressure dispersion function represented by Tempur World (Tempur World, Inc., Tempur World, Inc.), ordinary styrene or urethane resin is foamed. It is extremely flammable compared to mattresses and chairs using foam materials, but it is an internal structure of mattresses and chairs due to the flame retardant properties exhibited by the flame retardant composite used in the present invention. Fire spread to low-resilience urethane foam can be prevented.
布張り家具製品に対する本発明の難燃繊維複合体の用い方としては、表面の布地に織布やニットの形態で用いてもよいし、表面の布地と内部構造物、例えばウレタンフォームや詰め綿の間に織布やニット、不織布の形態で挟み込んでも良い。表面の布地に用いる場合には従来の表面の布地に替えて本発明の難燃繊維複合体よりなる布地を用いればよい。また、表面生地と内部構造物の間に織布やニットを挟む場合には、表面生地を2枚重ねる要領で挟み込んでも良いし、内部構造物を本発明の難燃繊維複合体よりなる織布やニットで覆っても良い。表面生地と内部構造物の間に炎遮蔽バリア用布織布として挟む場合には、内部構造物全体に、少なくとも表面の布地と接する部分については必ず内部構造物の外側に本発明の難燃繊維複合体よりなる不織布をかぶせ、その上から表面の布地を張ることになる。 As a method of using the flame-retardant fiber composite of the present invention for upholstered furniture products, the surface fabric may be used in the form of woven fabric or knit, or the surface fabric and internal structure such as urethane foam or stuffed cotton. It may be sandwiched in the form of woven fabric, knit or non-woven fabric. When used for the surface fabric, the fabric made of the flame retardant fiber composite of the present invention may be used instead of the conventional surface fabric. In addition, when a woven fabric or a knit is sandwiched between the surface fabric and the internal structure, the surface fabric may be sandwiched in the manner of overlapping two sheets, or the internal structure is a woven fabric made of the flame retardant fiber composite of the present invention. Or it may be covered with knit. When sandwiched between the surface fabric and the internal structure as a woven fabric for a flame-shielding barrier, the flame retardant fiber of the present invention must be placed on the entire internal structure, and at least the portion in contact with the surface fabric outside the internal structure. A non-woven fabric made of a composite is covered, and the surface fabric is stretched over it.
本発明の難燃繊維複合体は、ハロゲン含有難燃性合成繊維(A)、天然繊維および/または化学繊維(B)が複合したものであり、織物編物、不織布などの布帛、スライバーやウエブなどの繊維の集合体、紡績糸や合糸・撚糸などの糸状物、編み紐、組み紐などのヒモ状物のごとき形態のものである。 The flame retardant fiber composite of the present invention is a composite of halogen-containing flame retardant synthetic fiber (A), natural fiber and / or chemical fiber (B), and is a fabric such as a woven fabric or a non-woven fabric, a sliver or a web. Fiber aggregates, yarns such as spun yarns, synthetic yarns and twisted yarns, and string-like materials such as braids and braids.
前記複合したとは、繊維(A)、(B)をさまざまな方法で混ぜ合わせて所定の比率で含有する布帛などを得ることをいい、混綿、紡績、撚糸、織り、編みの段階でそれぞれの繊維や糸を組み合わせることを意味する。 The composite means that the fibers (A) and (B) are mixed by various methods to obtain a cloth containing the fibers in a predetermined ratio, and each of the mixed cotton, spinning, twisting, weaving and knitting stages. It means combining fiber and yarn.
本発明に用いうる難燃繊維複合体は炎遮蔽バリア用不織布として好適に用いられる。ここでいう炎遮蔽バリアとは、難燃性不織布が炎に晒された際に難燃性不織布が繊維の形態を維持したまま炭化することで炎を遮蔽し、反対側に炎が移るのを防ぐことであり、具体的にはマットレス、椅子、ソファー等の布張り家具等の表面生地と内部構造体であるウレタンフォームや詰め綿等との間に本発明の難燃性不織布をはさむことで、火災の際に内部構造物への炎の着火を防ぎ、被害を最小限に食い止めることができるものである。難燃性不織布の製造方法としては一般的なサーマルボンド法、ケミカルボンド法、ウォータージェット法、ニードルパンチ法、ステッチボンド法等の不織布作成方法が用いることが可能であり、複数の種類の繊維を混綿した後にカードにより開繊、ウェブ作成を行い、このウェブを不織布製造装置にかけることにより作成される。装置の簡便さからはニードルパンチ方式、ポリエステル系低融点バインダー繊維を用いる場合であればサーマルボンド方式による製造が一般的であるが、これらの方式に限定されるものではない。 The flame retardant fiber composite that can be used in the present invention is suitably used as a nonwoven fabric for a flame shielding barrier. The flame-shielding barrier here means that when the flame-retardant nonwoven fabric is exposed to flame, the flame-retardant nonwoven fabric is carbonized while maintaining the fiber form to shield the flame, and the flame moves to the opposite side. Specifically, by sandwiching the flame-retardant nonwoven fabric of the present invention between a surface fabric such as upholstered furniture such as a mattress, chair, sofa, etc. and urethane foam or stuffed cotton which is an internal structure In the event of a fire, the internal structure can be prevented from igniting flames and the damage can be minimized. Non-woven fabric creation methods such as general thermal bond method, chemical bond method, water jet method, needle punch method, stitch bond method and the like can be used as a method for producing a flame retardant nonwoven fabric. After blending, it is created by opening a card with a card and creating a web and applying the web to a nonwoven fabric manufacturing apparatus. In view of the simplicity of the apparatus, the production by the thermal bond method is common if the needle punch method or the polyester-based low melting point binder fiber is used, but it is not limited to these methods.
本発明の難燃繊維複合体には、必要に応じて帯電防止剤、熱着色防止剤、耐光性向上剤、白度向上剤、失透性防止剤などを含有せしめてもよい。 The flame retardant fiber composite of the present invention may contain an antistatic agent, a thermal coloration preventing agent, a light fastness improving agent, a whiteness improving agent, a devitrification preventing agent and the like as necessary.
このようにして得られる本発明の難燃繊維複合体は、所望の難燃性を有し、風合い、触感、吸湿性、意匠性などに優れた特性を有する。 The flame retardant fiber composite of the present invention thus obtained has desired flame retardancy and has excellent properties such as texture, touch, hygroscopicity, and design.
本発明の難燃繊維複合体を用いて布張り家具を製造すると、本発明の難燃繊維複合体が有する優れた特性、すなわち優れた難燃性を有し、風合い、触感、吸湿性、意匠性などの優れた特性を有する布張り家具製品が得られる。
本発明の難燃性合成繊維は短繊維でも長繊維でもよく、使用方法において適宜選択することが可能であり、例えば他の天然繊維および化学繊維と複合させて加工するには複合させる繊維に近似なものが好ましく、繊維製品用途に使用される他の天然繊維および化学繊維に合わせて、1.7〜12dtex程度、カット長38〜128mm程度の短繊維が好ましい。When producing upholstered furniture using the flame-retardant fiber composite of the present invention, the flame-retardant fiber composite of the present invention has excellent characteristics, that is, excellent flame retardancy, texture, touch, moisture absorption, design Upholstered furniture products having excellent properties such as properties can be obtained.
The flame-retardant synthetic fiber of the present invention may be a short fiber or a long fiber, and can be appropriately selected in the method of use. For example, it is similar to a fiber to be combined to be processed with other natural fibers and chemical fibers. It is preferable to use short fibers having a length of about 1.7 to 12 dtex and a cut length of about 38 to 128 mm in accordance with other natural fibers and chemical fibers used for textile products.
本発明の難燃性合成繊維が高度に優れた難燃性を示す理由は、以下のように考えられる。熱可塑性樹脂100重量部に対しガラス成分5〜49重量部、アンチモン化合物1〜45重量部を含有させた繊維を他の火炎源により燃焼させると重合体の成分は燃焼するが、重合体中のハロゲン原子と含有しているアンチモン化合物と反応して生成する不燃性ガスにより酸素が遮断され燃焼が抑制される(自己消火性)ため、焼失、焼損することなく炭化物となる。また燃焼時にガラス成分は溶融するのみで焼失しない。溶融したガラス成分は、重合体の燃焼により生成した炭化物間に入り込み、固化することで強固な炭化層を形成する(炭化効果)。これらの結果、前記繊維は燃焼後も崩壊することなく炭化物の状態で形態を保持するので、火炎は遮断されそれ以上の延焼が抑制されることで高度に優れた難燃性を示す。 The reason why the flame-retardant synthetic fiber of the present invention exhibits highly excellent flame retardancy is considered as follows. When a fiber containing 5 to 49 parts by weight of a glass component and 1 to 45 parts by weight of an antimony compound is burned by another flame source with respect to 100 parts by weight of a thermoplastic resin, the components of the polymer are burned. Oxygen is blocked by the non-combustible gas generated by reacting with the halogen atom and the antimony compound contained therein to suppress combustion (self-extinguishing property), so that it becomes a carbide without burning out or burning. In addition, the glass component only melts during combustion and does not burn out. The molten glass component enters between the carbides generated by the combustion of the polymer and solidifies to form a strong carbonized layer (carbonization effect). As a result, the fiber retains its form in the form of carbides without being disintegrated after combustion, so that the flame is cut off and further fire spread is suppressed, thereby exhibiting highly excellent flame retardancy.
本発明に用いる天然繊維および/または化学繊維(B)は、本発明の難燃性布帛に優れた風合、触感、意匠性、製品強力、耐洗濯性、耐久性を与えるための、また、寝具や家具に難燃性不織布を用いる際の加工性を良好にする成分である。 The natural fiber and / or chemical fiber (B) used in the present invention is for imparting excellent texture, touch, design, product strength, washing resistance and durability to the flame retardant fabric of the present invention. It is a component that improves processability when using a flame-retardant nonwoven fabric for bedding and furniture.
前記天然繊維の具体例としては、例えば綿、麻、などの植物性繊維や、羊毛、らくだ毛、山羊毛、絹などの動物繊維など、また化学繊維の具体例としては、たとえばビスコースレーヨン繊維、キュプラ繊維などの再生繊維、アセテート繊維などの半合成繊維、あるいはナイロン繊維、ポリエステル繊維、ポリエステル系低融点バインダー繊維、アクリル繊維などの合成繊維などがあげられるが、これらに限定されるものではない。これら天然繊維や化学繊維は単独で難燃性合成繊維(A)と用いてもよく、2種類以上で難燃性合成繊維(A)と用いてもよい。 Specific examples of the natural fibers include plant fibers such as cotton and hemp, animal fibers such as wool, camel hair, goat wool, and silk, and specific examples of chemical fibers include viscose rayon fibers. , Recycled fibers such as cupra fibers, semi-synthetic fibers such as acetate fibers, or synthetic fibers such as nylon fibers, polyester fibers, polyester-based low melting point binder fibers, and acrylic fibers, but are not limited thereto. . These natural fibers and chemical fibers may be used alone with the flame retardant synthetic fiber (A), or two or more types may be used with the flame retardant synthetic fiber (A).
ここでポリエステル系繊維は燃焼時に溶融物が生じ、難燃性不織布を覆うことで難燃性不織布により形成される炭化層がより強固なものとなり、激しい炎に長時間晒されても寝具や家具に用いられる綿やウレタンフォームへの着炎を防ぐ炎遮蔽バリア性能を付与することが出来ること、不織布に加工した際の嵩高性が得やすいこと、開繊機(カード)においてハロゲン含有難燃性合成繊維の強度の問題から繊維が破損することを緩和することから好ましい。ポリエステル系低融点バインダー繊維を用いると、不織布とする際に簡便な熱溶融接着法が採用できる。ポリエステル系低融点バインダー繊維としては、低融点ポリエステル単一型繊維でもよくポリエステル/低融点ポリプロピレン、低融点ポリエチレン、低融点ポリエステルからなる並列型もしくは芯鞘型複合型繊維でも良い。一般的に低融点ポリエステルの融点は概ね110〜200℃、低融点ポリプロピレンの融点は概ね140〜160℃、低融点ポリエチレンの融点は概ね95〜130℃であり、概ね110〜200℃程度で融解接着能力を有するものであれば特に限定はない。また低融点でないポリエステル系繊維を使用した場合、不織布とする際簡便なニードルパンチ法が採用できる。 Here, polyester fiber melts when burned, and the carbonized layer formed by the flame-retardant nonwoven fabric becomes stronger by covering the flame-retardant nonwoven fabric, so that bedding and furniture can be used even if exposed to intense flames for a long time. Can provide flame-shielding barrier performance to prevent flames on cotton and urethane foam used in the fabric, it is easy to obtain bulkiness when processed into non-woven fabric, and halogen-containing flame retardant synthesis in the opening machine (card) It is preferable because the damage of the fiber is eased due to the problem of the strength of the fiber. When a polyester-based low-melting-point binder fiber is used, a simple hot-melt bonding method can be adopted when forming a nonwoven fabric. The polyester-based low-melting-point binder fiber may be a low-melting-point polyester single-type fiber or a parallel-type or core-sheath-type composite fiber made of polyester / low-melting-point polypropylene, low-melting-point polyethylene, or low-melting-point polyester. Generally, the melting point of low-melting polyester is approximately 110 to 200 ° C, the melting point of low-melting polypropylene is approximately 140 to 160 ° C, and the melting point of low-melting polyethylene is approximately 95 to 130 ° C. There is no particular limitation as long as it has the ability. In addition, when a polyester fiber having a low melting point is used, a simple needle punch method can be employed when forming a nonwoven fabric.
本発明においては難燃性合成繊維(A)10重量部以上と天然繊維および/または化学繊維(B)90重量部以下とから、本発明の難燃性布帛100重量部が製造されるが、それらの混合割合は、得られる難燃性不織布から製造される最終製品に要求される難燃性とともに、吸水性、風合、吸湿性、触感、意匠性、製品強力、耐洗濯性、耐久性などの品質に応じて決定される。一般に、難燃性合成繊維(A)95〜10重量部、好ましくは60〜20重量部、天然繊維および/または化学繊維(B)5〜90重量部、好ましくは80〜40重量部の合計が100重量部になるように複合せしめられる。不織布製造の際に熱溶融接着法を選択する場合には、天然繊維および/または化学繊維(B)として、ポリエステル系低融点バインダー繊維を少なくとも10重量部含むことが好ましい。 In the present invention, 100 parts by weight of the flame-retardant fabric of the present invention is produced from 10 parts by weight or more of the flame-retardant synthetic fiber (A) and 90 parts by weight or less of the natural fiber and / or chemical fiber (B). The mixing ratio is the water resistance, texture, moisture absorption, touch, design, product strength, washing resistance, durability, as well as the flame resistance required for the final product manufactured from the resulting flame retardant nonwoven fabric. It is determined according to the quality. In general, the flame retardant synthetic fiber (A) 95 to 10 parts by weight, preferably 60 to 20 parts by weight, natural fiber and / or chemical fiber (B) 5 to 90 parts by weight, preferably 80 to 40 parts by weight. The composite is made to be 100 parts by weight. When the hot melt bonding method is selected during the production of the nonwoven fabric, it is preferable that at least 10 parts by weight of polyester-based low-melting-point binder fibers are included as natural fibers and / or chemical fibers (B).
難燃性合成繊維(A)の量が10重量部未満の場合、激しい炎に長時間晒されたときに寝具や家具に用いられる綿やウレタンフォームへの着炎を防ぐための炭化層形成が不充分で自己消火性にも乏しいため耐火性能が充分でなくなる。 When the amount of the flame retardant synthetic fiber (A) is less than 10 parts by weight, the formation of a carbonized layer for preventing flames from being applied to cotton and urethane foam used for bedding and furniture when exposed to intense flames for a long time. Insufficient and poor self-extinguishing properties, fire resistance is not sufficient.
本発明の難燃繊維複合体が高度に優れた難燃性を示す理由は、以下のように考えられる。難燃性合成繊維(A)を他の火炎源により燃焼させると重合体の成分は燃焼するが、含有しているアンチモン化合物から発生する不燃性ガスにより燃焼が抑制される(自己消火性)ため、焼失、焼損することなく炭化物となる。また燃焼時にガラス成分は溶融するのみで焼失せず、その溶融により難燃性合成繊維(A)や天然繊維および/または化学繊維(B)の燃焼により生成した炭化物層間に入り込み、強固な炭化層を形成する(炭化効果)。これらの結果、難燃繊維複合体は崩壊することなくその形態を保持するので、火炎はそれ以上延焼せず高度に優れた難燃性を示す。 The reason why the flame retardant fiber composite of the present invention exhibits highly excellent flame retardancy is considered as follows. When the flame retardant synthetic fiber (A) is combusted by another flame source, the polymer components are combusted, but the combustion is suppressed by the incombustible gas generated from the contained antimony compound (self-extinguishing property). It becomes a carbide without burning out or burning. In addition, the glass component only melts at the time of combustion, and does not burn out, and enters the carbide layer formed by the combustion of the flame retardant synthetic fiber (A) and natural fiber and / or chemical fiber (B), thereby a strong carbonized layer (Carbonization effect). As a result, since the flame retardant fiber composite retains its form without collapsing, the flame does not spread any further and exhibits a highly excellent flame retardancy.
本発明の難燃繊維複合体は炎遮蔽バリア用不織布として好適に用いられる。ここでいう炎遮蔽バリアとは、難燃性不織布が炎に晒された際に難燃性不織布が繊維の形態を維持したまま炭化することで炎を遮蔽し、反対側に炎が移るのを防ぐことであり、具体的にはマットレスや布張り家具等の表面生地と内部構造体であるウレタンフォームや詰め綿等との間に本発明の難燃性不織布をはさむことで、火災の際に内部構造物への炎の着火を防ぎ、被害を最小限に食い止めることができるものである。難燃性不織布の製造方法としては一般的な熱溶融接着法、ケミカルボンド法、ウォータージェット法、ニードルパンチ法、ステッチボンド法等の不織布作成方法が用いることが可能であり、複数の種類の繊維を混綿した後にカードにより開繊、ウェブ作成を行い、このウェブを不織布製造装置にかけることにより作成される。装置の簡便さからはニードルパンチ方式、ポリエステル系低融点バインダー繊維を用れば熱溶融接着方式による製造が一般的で生産性が高いため好ましいがこれらに限定されるものではない。 The flame retardant fiber composite of the present invention is suitably used as a nonwoven fabric for flame shielding barriers. The flame-shielding barrier here means that when the flame-retardant nonwoven fabric is exposed to flame, the flame-retardant nonwoven fabric is carbonized while maintaining the fiber form to shield the flame, and the flame moves to the opposite side. Specifically, in the event of a fire, the flame-retardant nonwoven fabric of the present invention is sandwiched between a surface fabric such as a mattress or upholstered furniture and an internal structure such as urethane foam or stuffed cotton. This prevents flames from igniting internal structures and minimizes damage. As a method for producing a flame retardant nonwoven fabric, nonwoven fabric creation methods such as a general hot melt bonding method, chemical bond method, water jet method, needle punch method, stitch bond method and the like can be used. After the cotton is blended, it is opened by a card, a web is created, and the web is applied to a nonwoven fabric manufacturing apparatus. From the viewpoint of simplicity of the apparatus, it is preferable to use a needle punch method or a polyester-based low-melting-point binder fiber because the production by the hot melt bonding method is general and the productivity is high, but it is not limited thereto.
本発明の難燃繊維複合体には、必要に応じて帯電防止剤、熱着色防止剤、耐光性向上剤、白度向上剤、失透性防止剤などを含有せしめてもよいし、染料や顔料などによる着色や染色を行っても何ら支障ない。 The flame retardant fiber composite of the present invention may contain an antistatic agent, a thermal coloring inhibitor, a light fastness improver, a whiteness improver, a devitrification preventive agent, and the like as necessary. There is no problem with coloring or dyeing with pigments.
このようにして得られる本発明の難燃繊維複合体は、所望の難燃性を有し、風合い、触感、吸湿性、意匠性などに優れた特性を有する。 The flame retardant fiber composite of the present invention thus obtained has desired flame retardancy and has excellent properties such as texture, touch, hygroscopicity, and design.
前記難燃繊維複合体は、高度な難燃性が要求され、かつ風合い、吸湿性、触感、意匠性などの一般的な繊維特性に優れていることが必要とされる意匠性のある布張り家具製品の用途に使用されるものである。 The flame retardant fiber composite is required to have a high degree of flame retardancy, and has a designable fabric tension that is required to have excellent general fiber characteristics such as texture, moisture absorption, touch, and design. Used for furniture products.
布張り家具製品に対する本発明の難燃繊維複合体の用い方としては、表面の布地に織布やニットの形態で用いてもよいし、表面の布地と内部構造物、例えばウレタンフォームや詰め綿の間に織布やニット、不織布の形態で挟み込んでも良い。表面の布地に用いる場合には従来の表面の布地に替えて本発明の難燃繊維複合体よりなる布地を用いればよい。また、表面生地と内部構造物の間に織布やニットを挟む場合には、表面生地を2枚重ねる要領で挟み込んでも良いし、内部構造物を本発明の難燃繊維複合体よりなる織布やニットで覆っても良い。表面生地と内部構造物の間に炎遮蔽バリア用布織布として挟む場合には、内部構造物全体に、少なくとも表面の布地と接する部分については必ず内部構造物の外側に本発明の難燃繊維複合体よりなる不織布をかぶせ、その上から表面の布地を張る。 As a method of using the flame-retardant fiber composite of the present invention for upholstered furniture products, the surface fabric may be used in the form of woven fabric or knit, or the surface fabric and internal structure such as urethane foam or stuffed cotton. It may be sandwiched in the form of woven fabric, knit or non-woven fabric. When used for the surface fabric, the fabric made of the flame retardant fiber composite of the present invention may be used instead of the conventional surface fabric. In addition, when a woven fabric or a knit is sandwiched between the surface fabric and the internal structure, the surface fabric may be sandwiched in the manner of overlapping two sheets, or the internal structure is a woven fabric made of the flame retardant fiber composite of the present invention. Or it may be covered with knit. When sandwiched between the surface fabric and the internal structure as a woven fabric for a flame-shielding barrier, the flame retardant fiber of the present invention must be placed on the entire internal structure, and at least the portion in contact with the surface fabric outside the internal structure. Cover the non-woven fabric made of the composite, and stretch the surface fabric over it.
以下、難燃性合成繊維及び難燃繊維複合体の実施例をあげて本発明をさらに詳しく説明するが、本発明はかかる実施例のみに限定されるものではない。なお実施例における繊維の難燃性は繊維単独及び不織布又は不織布複合体を用いて下記のようにして測定した。
(不織布による難燃性評価)
(難燃性評価試験用不織布の作成)
繊維をローラーカードにより開繊した後、ニードルパンチ法により、目付け200g/m2、縦20cm×横20cmの不織布を作成した。
(難燃性評価試験方法)
縦200mm×横200mm×厚さ10mmのパーライト板の中心に直径15cmの穴をあけたものを準備し、その上に難燃性評価試験用不織布を置き、加熱時に難燃性評価試験用不織布が収縮しないよう4辺をクリップで固定した。この試料を難燃性評価試験用不織布の面を上にして、ガスコンロ((株)パロマ工業製PA−10H−2)にバーナー面より40mmの所に試料の中心とバーナーの中心が合うようにセットした。燃料ガスは純度99%以上のプロパンを用い、炎の高さは25mmとし、着炎時間は180秒とした。この時に難燃性評価試験用不織布又は複合試験体の炭化層に貫通した穴があいていない場合、またはひびがない場合を合格○、穴やひびがある場合を不合格×として評価を実施した。
(LOI値による難燃性評価)
以下の製造例に従って作成した綿を2g取り、これを8等分して約6cmのコヨリを8本作成し酸素指数測定器のホルダーに直立させ、この試料が5cm燃え続けるのに必要な最小酸素濃度を測定し、これをLOI値とした。LOI値が大きいほど燃えにくく、難燃性が高い。
(繊維中のハロゲン含有量の測定方法)
得られた共重合体を(株)柳本製作所製ヤナコCHNコーダーMT−5によりC元素、H元素、N元素に関する元素分析を行い、N原子をアクリロニトリル由来のものとし、N原子含有量より重合体中のアクリロニトリル成分含有量を求めた。さらにp−スチレンスルホン酸ソーダは全量共重合したと仮定し、残りをハロゲンモノマー由来成分とし、計算により得られたハロゲン含有共重合体中のハロゲン含有量を求めた。
(製造例1)
アクリロニトリル51%、塩化ビニリデン48%およびp−スチレンスルホン酸ソーダ1%よりなる共重合体(ハロゲン原子割合:35%)をジメチルホルムアミドに樹脂濃度が30%になるように溶解させ、得られた樹脂溶液の樹脂重量に対して表1に示す添加量においてガラス成分(P2O5−ZnO系 旭ファイバーグラス(株)製 ZP150 ガラス転移温度約350℃)と三酸化アンチモンを添加し、紡糸原液とした。ガラス成分および三酸化アンチモンを含んだ紡糸原液をノズル孔径0.10mmおよび孔数1000ホールのノズルを用い、50%ジメチルホルムアミド水溶液中へ押し出し、水洗したのち120℃で乾燥し、ついで3倍に延伸してから、さらに150℃で5分間熱処理、さらに切断することでハロゲン含有繊維を得た。得られた繊維は繊度5.6dtexであり、カット長51mmの短繊維であった。
(実施例1〜3、比較例1〜2)
製造例1に従い、ガラス成分と三酸化アンチモンを表1の量で添加したハロゲン含有繊維を作成し、不織布およびLOI値での難燃性評価を実施した。結果を表1に示す。Hereinafter, the present invention will be described in more detail with reference to examples of the flame-retardant synthetic fiber and the flame-retardant fiber composite, but the present invention is not limited to such examples. In addition, the flame retardance of the fiber in an Example was measured as follows using the fiber alone and the nonwoven fabric or the nonwoven fabric composite.
(Flame resistance evaluation by non-woven fabric)
(Preparation of non-woven fabric for flame retardant evaluation test)
After opening the fiber with a roller card, a nonwoven fabric having a basis weight of 200 g / m 2 and a length of 20 cm × width of 20 cm was prepared by a needle punch method.
(Flame retardancy evaluation test method)
Prepare a pearlite plate with a length of 200 mm × width 200 mm × thickness 10 mm with a hole with a diameter of 15 cm, and place a non-woven fabric for flame retardancy evaluation test on it. Four sides were fixed with clips so as not to shrink. With this sample facing the non-woven fabric for flame retardancy evaluation test, the center of the sample and the center of the burner are aligned with a gas stove (PA-10H-2 manufactured by Paloma Kogyo Co., Ltd.) 40 mm from the burner surface. I set it. The fuel gas used was propane with a purity of 99% or more, the flame height was 25 mm, and the flame time was 180 seconds. At this time, the evaluation was carried out with a case where there was no through-hole or no crack in the carbonized layer of the flame retardant evaluation test non-woven fabric or composite test piece, and a case where there was a hole or a crack. .
(Flame resistance evaluation by LOI value)
Take 2g of cotton prepared according to the following production example, divide this into 8 equal parts, make 8 cisterns of about 6cm, stand upright on the holder of the oxygen index measuring instrument, and the minimum oxygen necessary for this sample to keep burning 5cm The concentration was measured and used as the LOI value. The larger the LOI value, the harder to burn and the higher the flame retardancy.
(Measurement method of halogen content in fiber)
The obtained copolymer was subjected to elemental analysis on C element, H element and N element by Yanako CHN coder MT-5 manufactured by Yanagimoto Seisakusho Co., Ltd., and N atom was derived from acrylonitrile, and the polymer was determined from the N atom content. The acrylonitrile component content in it was determined. Further, it was assumed that the total amount of p-styrene sulfonic acid soda was copolymerized, the remainder was regarded as a component derived from a halogen monomer, and the halogen content in the halogen-containing copolymer obtained by calculation was determined.
(Production Example 1)
A resin obtained by dissolving a copolymer (halogen atom ratio: 35%) of 51% acrylonitrile, 48% vinylidene chloride and 1% p-styrenesulfonic acid soda in dimethylformamide so that the resin concentration is 30%. Glass components (P2O5-ZnO system manufactured by Asahi Fiber Glass Co., Ltd., ZP150 glass transition temperature of about 350 ° C.) and antimony trioxide were added to the resin weight of the solution to obtain a spinning dope. The spinning solution containing the glass component and antimony trioxide was extruded into a 50% dimethylformamide aqueous solution using a nozzle with a nozzle hole diameter of 0.10 mm and a hole number of 1000 holes, washed with water, dried at 120 ° C., and then stretched 3 times. Then, a halogen-containing fiber was obtained by further heat treatment at 150 ° C. for 5 minutes and further cutting. The obtained fiber was a fine fiber having a fineness of 5.6 dtex and a cut length of 51 mm.
(Examples 1-3, Comparative Examples 1-2)
In accordance with Production Example 1, a halogen-containing fiber having a glass component and antimony trioxide added in the amounts shown in Table 1 was prepared, and the flame resistance was evaluated using a nonwoven fabric and LOI value. The results are shown in Table 1.
実施例1〜3、および比較例1〜2の難燃性評価試験結果
実施例1〜3の燃焼試験結果は良好であり、難燃性評価試験用不織布はガスコンロによる加熱後、良好な炭化層を形成し、残炎や亀裂、穴明きの発生はなく、総合判定は合格した。これに対して比較例1は、三酸化アンチモン量は実施例1と同量であるがガラス成分が少ないため良好な炭化層が形成できず不織布に穴が生じ、総合判定が不合格となった。比較例2は添加剤の合計量は実施例1と同量であり、LOI値は同程度だがガラス成分の量が少ないため良好な炭化層が形成できず不織布に穴が生じ、総合判定が不合格となった。
(実施例4〜6、比較例3〜5)
製造例に従い、ガラス成分と三酸化アンチモンを表2の量で添加したハロゲン含有繊維を作成し、本発明繊維80重量部、ポリエステル繊維(東洋紡績(株)製 6.6dtex カット長51mm)20重量部を混合した不織布の難燃性評価を実施した。結果を表2に示す。Flame retardancy evaluation test results of Examples 1 to 3 and Comparative Examples 1 to 2 The flame test results of Examples 1 to 3 are good, and the nonwoven fabric for flame retardancy evaluation test is a good carbonized layer after heating with a gas stove , And there was no after-flame, cracks or perforations, and the overall judgment passed. On the other hand, in Comparative Example 1, the amount of antimony trioxide was the same as that in Example 1, but since the glass component was small, a good carbonized layer could not be formed, a hole was formed in the nonwoven fabric, and the overall judgment was rejected. . In Comparative Example 2, the total amount of additives is the same as Example 1, and the LOI value is about the same, but the amount of glass component is small, so that a good carbonized layer cannot be formed, and a hole is formed in the nonwoven fabric, making the overall judgment unsatisfactory. Passed.
(Examples 4-6, Comparative Examples 3-5)
In accordance with the production example, a halogen-containing fiber having a glass component and antimony trioxide added in the amounts shown in Table 2 was prepared, and 80 parts by weight of the present fiber and 20% by weight of polyester fiber (6.6 dtex cut length 51 mm, manufactured by Toyobo Co., Ltd.). The flame retardancy evaluation of the nonwoven fabric mixed with the part was carried out. The results are shown in Table 2.
実施例4〜6、および比較例3〜5の難燃性評価試験結果
実施例4〜6の燃焼試験結果は良好であり、難燃性評価試験用不織布はガスコンロによる加熱後、良好な炭化層を形成し、残炎や亀裂、穴明きの発生はなかった。これに対して比較例3は、三酸化アンチモン量は実施例4と同量であるがガラス成分が少ないため良好な炭化層が形成できず、不織布に穴が生じた。比較例5、6は添加剤の合計量は実施例4と同量であるが、ガラス成分の量が少ないため良好な炭化層が形成できず不織布に穴が生じた。
さらに、実施例をあげて本発明をさらに詳しく説明するが、本発明はかかる実施例のみに限定されるものではない。なお実施例における繊維の難燃性は不織布を用いて下記のようにして測定した。これは、マットレス、椅子、ソファー等の布張り家具等の表面生地と内部構造体であるウレタンフォームや詰め綿等との間に本発明の難燃性不織布をはさむことで、火災の際に寝具や家具の内部構造物への炎の着火を防ぐことを想定した簡易評価方法である。
(不織布複合体による難燃性評価)
(難燃性評価試験用不織布複合体の作成)
所定の割合で混合した繊維をカードにより開繊した後、ニードルパンチ法により、目付け200g/m2、縦20cm×横20cmの不織布を作成した。表面生地としてポリエステル製織布(目付120g/cm2)で該不織布全面を包み、難燃性評価試験用不織布
複合体とした。
(不織布複合体による難燃性評価試験方法)
縦200mm×横200mm×厚さ10mmのパーライト板の中心に直径15cmの穴をあけたものを準備し、その上に難燃性評価試験用不織布複合体をセットし、加熱時に難燃性評価試験用不織布複合体が収縮しないよう4辺をクリップで固定した。この試料を難燃性評価試験用不織布複合体の面を上にして、株式会社パロマ工業製ガスコンロ(PA−10H−2)にバーナー面より40mmの所に試料の中心とバーナーの中心が合うようにセットした。燃料ガスは純度99%以上のプロパンを用い、炎の高さは25mmとし、着炎時間は180秒とした。この時に難燃性評価試験用不織布複合体の炭化膜の厚み斑がなく全く穴やひびがない場合を合格◎、炭化膜に貫通した穴があいていない場合、またはひびがない場合を合格○、穴やひびがある場合を不合格×として評価を実施した。
(製造例2)
アクリロニトリル51%、塩化ビニリデン48%およびp−スチレンスルホン酸ソーダ1%よりなる共重合体(ハロゲン原子割合:35%)をジメチルホルムアミドに樹脂濃度が30%になるように溶解させ、得られた樹脂溶液の樹脂重量に対して表3に示す添加量においてガラス成分(P2O5−ZnO系 旭ファイバーグラス(株)製 ZP150 ガラス転移温度約350℃)と三酸化アンチモンを添加し、紡糸原液とした。Flame retardancy evaluation test results of Examples 4 to 6 and Comparative Examples 3 to 5 The flame test results of Examples 4 to 6 are good, and the nonwoven fabric for flame retardancy evaluation test is a good carbonized layer after heating with a gas stove There was no afterflame, cracks, or perforations. On the other hand, in Comparative Example 3, the amount of antimony trioxide was the same as that in Example 4, but a good carbonized layer could not be formed because the glass component was small, and holes were formed in the nonwoven fabric. In Comparative Examples 5 and 6, the total amount of the additive was the same as that in Example 4, but since the amount of the glass component was small, a good carbonized layer could not be formed and holes were formed in the nonwoven fabric.
Furthermore, although an Example is given and this invention is demonstrated in more detail, this invention is not limited only to this Example. In addition, the flame retardance of the fiber in an Example was measured as follows using the nonwoven fabric. This is because the flame retardant nonwoven fabric of the present invention is sandwiched between a surface fabric such as upholstered furniture such as a mattress, a chair, a sofa, etc. and urethane foam or stuffed cotton which is an internal structure, so that bedding in the event of a fire It is a simple evaluation method that is supposed to prevent the ignition of the internal structure of furniture and furniture.
(Flame resistance evaluation by nonwoven fabric composite)
(Preparation of non-woven composite for flame retardant evaluation test)
After the fibers mixed at a predetermined ratio were opened with a card, a nonwoven fabric having a basis weight of 200 g / m 2 and a length of 20 cm × width 20 cm was prepared by a needle punch method. The entire surface of the nonwoven fabric was wrapped with a polyester woven fabric (weight per unit area: 120 g / cm 2 ) as a surface fabric to obtain a nonwoven fabric composite for flame retardancy evaluation test.
(Flame retardancy evaluation test method using nonwoven fabric composite)
Prepare a pearlite plate with a length of 200mm x width 200mm x thickness 10mm with a hole with a diameter of 15cm, set a non-woven composite for flame resistance evaluation test on it, and flame resistance evaluation test during heating Four sides were fixed with clips so that the nonwoven fabric composite for use did not shrink. With this sample facing the non-woven composite for flame retardancy evaluation test, the center of the sample and the center of the burner are aligned with a gas stove (PA-10H-2) manufactured by Paloma Industry Co., Ltd. at 40 mm from the burner surface. Set. The fuel gas used was propane with a purity of 99% or more, the flame height was 25 mm, and the flame time was 180 seconds. At this time, pass the case where there is no unevenness in the thickness of the carbonized film of the non-woven composite for flame retardancy evaluation test, and there are no holes or cracks. Pass the case where there are no holes or cracks in the carbonized film. In the case where there is a hole or a crack, the evaluation was made with a failure X.
(Production Example 2)
A resin obtained by dissolving a copolymer (halogen atom ratio: 35%) of 51% acrylonitrile, 48% vinylidene chloride and 1% p-styrenesulfonic acid soda in dimethylformamide so that the resin concentration is 30%. Glass components (P2O5-ZnO system manufactured by Asahi Fiber Glass Co., Ltd., ZP150 glass transition temperature of about 350 ° C.) and antimony trioxide were added to the resin weight of the solution to obtain a spinning dope.
このガラス成分および/または三酸化アンチモンを含んだ紡糸原液をノズル孔径0.10mmおよび孔数1000ホールのノズルを用い、50%ジメチルホルムアミド水溶液中へ押し出し、水洗したのち120℃で乾燥し、ついで3倍に延伸してから、さらに150℃で5分間熱処理を行なうことにより、ハロゲン含有繊維を得た。得られた繊維は繊度5.6dtex、カット長51mmの短繊維であった。
(実施例7〜12、比較例6〜9)
製造例2に従い、ガラス成分と三酸化アンチモンを表3の量で添加したハロゲン含有繊維を作成し、得られたハロゲン含有繊維、ポリエステル繊維(6.6dtex、カット長51mm)、レーヨン繊維(1.5dtex、カット長38mm)所定の割合で不織布を作成し、難燃性評価を実施した。結果を表3に示す。The spinning solution containing the glass component and / or antimony trioxide was extruded into a 50% dimethylformamide aqueous solution using a nozzle having a nozzle hole diameter of 0.10 mm and a hole number of 1000 holes, washed with water, dried at 120 ° C., and then 3 After drawing to double, a heat treatment was further performed at 150 ° C. for 5 minutes to obtain a halogen-containing fiber. The obtained fiber was a short fiber having a fineness of 5.6 dtex and a cut length of 51 mm.
(Examples 7-12, Comparative Examples 6-9)
In accordance with Production Example 2, a halogen-containing fiber was prepared by adding a glass component and antimony trioxide in the amounts shown in Table 3, and the resulting halogen-containing fiber, polyester fiber (6.6 dtex, cut length 51 mm), rayon fiber (1. (5 dtex, cut length 38 mm) Nonwoven fabric was prepared at a predetermined ratio, and flame retardancy evaluation was performed. The results are shown in Table 3.
実施例7〜12は燃焼試験結果が良好であり、難燃性評価試験用不織布複合体はガスコンロによる加熱後も亀裂や穴明きの発生がなく、良好な炭化膜を形成した。これに対して比較例6ではガラス成分が少ないため良好な炭化膜が形成できず、不織布に穴が生じた。 Examples 7 to 12 had good combustion test results, and the nonwoven fabric composite for flame retardancy evaluation test did not generate cracks or holes after heating with a gas stove, and formed a good carbonized film. On the other hand, in Comparative Example 6, since the glass component was small, a good carbonized film could not be formed, and holes were formed in the nonwoven fabric.
比較例7,8では難燃剤の合計量は実施例7と同量であるが、ガラス成分が含まれないために良好な炭化膜が形成できず、不織布に穴が生じた。 In Comparative Examples 7 and 8, the total amount of the flame retardant was the same as that in Example 7, but a good carbonized film could not be formed because the glass component was not included, and holes were formed in the nonwoven fabric.
比較例9では、実施例8,9に対してハロゲン含有繊維の量が少なく良好な炭化膜が形成されなかった。
In Comparative Example 9, a good carbonized film was not formed because the amount of halogen-containing fiber was small compared to Examples 8 and 9.
Claims (13)
前記ガラス成分が10〜40重量部でありかつ、前記アンチモン化合物が10〜35重量部である事を特徴とする難燃性合成繊維。A flame retardant synthetic fiber containing a total of 20 to 50 parts by weight of a glass component and an antimony compound with respect to 100 parts by weight of a polymer containing 17% by weight or more of a halogen atom ,
The flame-retardant synthetic fiber, wherein the glass component is 10 to 40 parts by weight and the antimony compound is 10 to 35 parts by weight .
前記ガラス成分が10〜40重量部でありかつ、前記アンチモン化合物が10〜35重量部である事を特徴とする難燃性合成繊維複合体。10 parts by weight or more of the flame retardant synthetic fiber (A) containing 20 to 50 parts by weight of the total of the glass component and the antimony compound with respect to 100 parts by weight of the polymer containing 17% by weight or more of halogen atoms, natural fiber and / or chemical A flame retardant fiber composite comprising 90 parts by weight or less of at least one kind of fiber (B) ,
The flame-retardant synthetic fiber composite, wherein the glass component is 10 to 40 parts by weight and the antimony compound is 10 to 35 parts by weight .
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| PCT/JP2005/013126 WO2006011379A1 (en) | 2004-07-30 | 2005-07-15 | Flame retardant synthetic fiber, flame retardant fiber composite, and cloth-lined furniture product using the same |
| JP2006529172A JP4777892B2 (en) | 2004-07-30 | 2005-07-15 | Flame retardant synthetic fiber, flame retardant fiber composite and upholstered furniture product using the same |
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Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63273690A (en) * | 1987-04-11 | 1988-11-10 | シープリー・プロダクツ・リミテッド | Flame retardant additive composition |
| JPH03294515A (en) * | 1990-04-09 | 1991-12-25 | Mitsubishi Rayon Co Ltd | Production of highly flame-retardant acrylic fiber having excellent transparency |
| JPH0860434A (en) * | 1994-08-12 | 1996-03-05 | Kanebo Ltd | Antibacterial acrylic synthetic fiber and its fiber product |
| JPH09221572A (en) * | 1996-02-14 | 1997-08-26 | Asahi Chem Ind Co Ltd | Agent for suppressing drip of live coals (fire source) or styrene resin composition |
| JP2003096619A (en) * | 2001-09-25 | 2003-04-03 | Kanebo Ltd | Acrylic synthetic fiber and fiber composite material made therefrom |
-
2005
- 2005-07-15 WO PCT/JP2005/013126 patent/WO2006011379A1/en not_active Ceased
- 2005-07-15 JP JP2006529172A patent/JP4777892B2/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63273690A (en) * | 1987-04-11 | 1988-11-10 | シープリー・プロダクツ・リミテッド | Flame retardant additive composition |
| JPH03294515A (en) * | 1990-04-09 | 1991-12-25 | Mitsubishi Rayon Co Ltd | Production of highly flame-retardant acrylic fiber having excellent transparency |
| JPH0860434A (en) * | 1994-08-12 | 1996-03-05 | Kanebo Ltd | Antibacterial acrylic synthetic fiber and its fiber product |
| JPH09221572A (en) * | 1996-02-14 | 1997-08-26 | Asahi Chem Ind Co Ltd | Agent for suppressing drip of live coals (fire source) or styrene resin composition |
| JP2003096619A (en) * | 2001-09-25 | 2003-04-03 | Kanebo Ltd | Acrylic synthetic fiber and fiber composite material made therefrom |
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| WO2006011379A1 (en) | 2006-02-02 |
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