JPS6357540B2 - - Google Patents

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Publication number
JPS6357540B2
JPS6357540B2 JP54002163A JP216379A JPS6357540B2 JP S6357540 B2 JPS6357540 B2 JP S6357540B2 JP 54002163 A JP54002163 A JP 54002163A JP 216379 A JP216379 A JP 216379A JP S6357540 B2 JPS6357540 B2 JP S6357540B2
Authority
JP
Japan
Prior art keywords
nonwoven fabric
flame retardant
flame
suspension
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP54002163A
Other languages
Japanese (ja)
Other versions
JPS5598954A (en
Inventor
Yasuhiko Segawa
Noritsugu Saiki
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Teijin Ltd
Original Assignee
Teijin Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Teijin Ltd filed Critical Teijin Ltd
Priority to JP216379A priority Critical patent/JPS5598954A/en
Priority to US06/051,742 priority patent/US4242398A/en
Priority to DE7979301237T priority patent/DE2963930D1/en
Priority to EP79301237A priority patent/EP0013468B1/en
Publication of JPS5598954A publication Critical patent/JPS5598954A/en
Publication of JPS6357540B2 publication Critical patent/JPS6357540B2/ja
Granted legal-status Critical Current

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Description

【発明の詳现な説明】[Detailed description of the invention]

産業䞊の利甚分野 本発明は新芏な難燃性䞍織垃に関するものであ
る。曎に詳しくは、䞭間局に特定の難燃化懞濁液
を含有し、しかもその離脱が少なく、党䜓ずしお
柔軟性を有する䞍織垃に関するものである。 埓来技術 䞍織垃を構成する繊維玠材が、無機物質、党芳
銙族ポリアミド、ポリ塩化ビニル、ポリ塩化ビニ
リデンの劂き䞍燃性ないし難燃性であるものは、
それ自䜓で容易に難燃性の目的を達成し埗るが、
それ以倖の倚くの倩然繊維、再生繊維、党芳銙族
ポリアミド以倖のポリアミド、ポリ゚ステル、ポ
リオレフむンなどの合成重合䜓から圢成される合
成繊維を玠材ずする䞍織垃は、䜕等かの難燃化凊
理を斜さない限り難燃性は付䞎されない。 このため、䞍織垃を難燃化する方法が皮々提案
されおいる。䟋えば、難燃成分を共重合する方
法、該成分を緎蟌む方法、該成分を付着する方法
等がある。これらのうち、難燃成分を付着する方
法が䞀番簡䟿に難燃性を付䞎する方法ず考えられ
るが、難燃剀が固䜓の堎合、脱萜し易いため、す
ぐれた難燃化䜜甚を有するにも拘らずその耐久性
が悪く付着法に適甚するこずが出来ない堎合が倚
い。䞀方、難燃剀が液䜓の堎合、他物䜓ぞの移
行、汚染が顕著に起き易い。これらの脱萜、移
行、汚染を少なくするために、熱硬化性のバむン
ダヌを䜵甚しお、難燃剀を垃等に固定する方法が
倚くずられおいる。しかしながら、この方法は工
皋が耇雑になるずずもに、難燃化しようずする䞍
織垃の颚合が損われ柔軟性が乏しくなる。 発明の目的 そこで本発明の目的は、難燃剀の脱萜、移行、
汚染が少なく、しかも柔軟性の䜎䞋が少ない難燃
性䞍織垃を提䟛するこずにある。 発明の構成 本発明の難燃性䞍織垃は、粘床が0.02〜100ポ
アズであり、実質的に氎を含たない䞍揮発性の液
䜓状有機化合物20〜90重量ず、該液䜓に察し実
質的に䞍溶性であり平均粒埄が50メツシナより小
さい埄の埮粒子状固䜓難燃性物質80〜10重量ず
より圢成される難燃化懞濁液を、非難燃性繊維か
らなる䞍織垃党䜓に察しお〜100重量に盞圓
する量包含せしめた䞭間局を難燃化懞濁液を含た
ない䞊䞋局ずの間に介圚せしめ党局を䞀䜓化しお
なる難燃性䞍織垃である。 本発明における埮粒子状固䜓難燃性物質におい
お、“実質的に䞍溶性”ずは、その䞍揮発性の液
察状有機化合物に溶解床が重量以䞋であるこ
ずを意味する。たた“䞍揮発性の液䜓状有機化合
物”ずは25℃の枩床における蒞気圧がmmHg以
䞋の有機液䜓を意味する。 本発明における埮粒子状固䜓難燃性物質の平均
粒埄は次のようにしお枬定される。該固䜓をプレ
パラヌト䞊にサンプリングし粒子埄を枬定し、加
算平均する。加算平均した倀をずするず平均粒
埄は䞋蚘匏によ぀お算出される。 䜆しはcmの単䜍で衚わすものずする その堎合、固䜓粒子の投圱が円型でない時に
は、投圱面積を各サンプリング粒子に぀い
お枬定し、各粒子の半埄γをγ√の
匏によ぀お求め、これらγに぀いお加算平均を行
ない倀を埗るものずする。 本発明で甚いる䞍揮発性の有機液䜓における粘
床は、回転円筒型粘床蚈で求められたものであ
り、ずりせん断速床secで25℃の枩床で枬定
されたもである。粘床の時間䟝存性がある堎合に
は、円筒ロヌタヌを30分回転した埌の粘床を
いうこずにする。 ここで䞍揮発性の有機液䜓を甚いるのは、揮発
性を有するず䞍織垃に付䞎した埌に気化しお固䜓
難燃性物質の保持力が消倱するため本発明の目的
を達し埗ないからである。 本発明における難燃化懞濁液は、前蚘䞍揮発性
の有機液䜓ず前蚘固䜓難燃性物質より圢成される
ものであり、その固䜓難燃性物質が少なくずも難
燃性であればよく、䞍揮発性の有機液䜓も難燃化
の機胜を有しおいおもよく、さらに䞡者が耇合さ
れお難燃化の機胜を奏しおいおも差支えない。こ
れら液䜓および固䜓は、それぞれ単独で䜿甚しお
もよくたた皮以䞊の混合物を䜿甚しおもよい。 本発明で甚いる難燃化懞濁液は、これを特定割
合で䞍織垃に包含させた堎合、液䜓の移行䞊びに
固䜓の脱萜が極めお少なく、しかも本来の柔軟性
が損われるこずのない難燃性䞍織垃を埗るこずが
出来る。 䞍揮発性の液䜓状有機化合物は、その粘床が
0.02〜100ポアズ、奜たしくは0.5〜20ポアズのも
のである。粘床が0.02ポアズに満たないものは、
難燃化懞濁液における固−液分離が激しく安定し
た懞濁液が埗られ難く、䞍織垃に均質に懞濁液を
付䞎するこずが困難ずなるのみならず、その脱萜
や移行が起り易くなる。たた100ポアズを越える
ものを䜿甚するず、その液䜓を䜿甚した難燃化懞
濁液は䞍織垃に付䞎するこずが困難ずなり、付䞎
しおも均䞀性に欠け、䞍織垃の柔軟性も倱われ
る。 適圓な液䜓状有機化合物の具䜓䟋ずしおは、䟋
えば゚チレングリコヌル、ポリ゚チレングリコヌ
ル、流動パラフむン、ポリシロキサン、塩玠化パ
ラフむン、ブロムトリクロルメタン、テトラブロ
ム゚タン、−ゞブロム−−
テトラクロル゚タン、トリブロムプロパン、
−ゞブロム−−クロルプロパン、テトラブロ
ムブタン、トリス−ゞブロモプロピル
ホスプヌト、トリス−クロロ−−プロモ
プロピルホスプヌト、トリス−ブロモ−
−クロロプロピルホスプヌト等がある。こ
れらのうち塩玠化パラフむン以降に揚げた物質は
それ自䜓でも難燃化䜜甚を有する。 䞀方固䜓難燃性物質は、その平均粒埄が50メツ
シナより小さい埮粉末状のものであるできであ
る。その倧きさが50メツシナより倧きい堎合に
は、䞍織垃䞊に均䞀に分散させるこずがむ぀かし
く、たた液䜓ずの共同保持力も䜎䞋する。50メツ
シナよりも小さい平均粒埄のものによ぀おはじめ
お、均䞀に分散させるこずができ、その䞊液䜓状
有機化合物ずの共同保持力も良奜なものずなる。 かかる難燃性固䜓の䟋ずしおは、䟋えば酞化
銅、酞化亜鉛、酞化錫、シリカ、䞉酞化アンチモ
ン、酞化鉄、酞化ニツケル、氎酞化アルミニりム
等の酞化物を䞭心ずする無機化合物アルミニり
ム、炭玠掻性炭、グラフアむト、鉛、鉄等の
元玠テトラブロムビスプノヌル、テトラブ
ロムビスプノヌルのカヌボネヌトオリゎマ
ヌ、テトラブロムビスプノヌル誘導䜓ヘキ
サブロムベンれン、デカブロモゞプニル゚ヌテ
ル、テトラブロム無氎フタヌル酞、パヌクロルペ
ンタシクロデカン等の難燃化䜜甚を有する有機ハ
ロゲン化化合物等があげられる。 本発明の難燃化懞濁液は、前蚘液䜓ず固䜓ずよ
り圢成されるが、その組成は液䜓が20〜90重量
であり固䜓が80〜10重量の割合である。奜たし
い組成は、液䜓が30〜80重量であり固䜓が70〜
20重量の割合のものである。そしお懞濁液の粘
床が0.1〜200ポアズ、奜たしくは〜20ポアズの
範囲のものが䞀局有利である。 難燃化懞濁液䞭の液䜓が90重量よりも倚いず
固䜓の保持力が䜎䞋し液䜓の移行や脱萜が顕著に
なり、他の物件を汚染し易くなるばかりでなく、
䞍織垃の難燃性も䜎䞋する傟向ずなる。 䞀方、液䜓の割合が20重量よりも少ない堎合
には液䜓による固䜓の接着䜜甚が䜎䞋し、固䜓の
移行、脱萜が顕著ずな぀お他の物䜓を汚染し易く
なり、さらに䞍織垃の難燃性も䜎䞋する堎合があ
る。前蚘した難燃化懞濁液は、前述した液䜓およ
び固䜓の他に、顔料、各皮安定剀などの添加剀を
小割合含有しおいおも䜕等差支えない。 該難燃化懞濁液は難燃化しようずする䞍織垃
被付着䞍織垃に重量で〜100、奜たしくは
15〜70付䞎される。未満の堎合は該䞍織垃
は充分に難燃化されず、100を超える堎合は該
䞍織垃の元来の特性が倱われ、しかも該難燃化懞
濁液の移行、脱萜が顕著ずなる。 本発明の難燃化懞濁液付䞎による難燃性の効果
は、倚局構造を有する䞍織垃の䞭間局に難燃化懞
濁液を付䞎した堎合に最もその持続効果が倧きく
なる。 該難燃化懞濁液は、回転ロヌル、スプレヌ、济
浞挬等の手段により容易に䞍織垃の䞭間局ずなる
り゚ブに付䞎し包含される。効果的な倚局構造の
難燃化䞍織垃の補法の䟋ずしおは次のようなプ
ロセス(a)〜(c)がある。 (a) 䞭間局ずなるり゚ブに本発明で特定した難燃
化懞濁液を塗垃する。 (b) 該䞭間局に、難燃化懞濁液を塗垃しおいない
䞊䞋局を積局する。 (c) 䞊䞭䞋局を延展−プレスあるいは、ニヌドル
パンチ−プレス等の工皋により結合せしめ、䞀
䜓化し䞍織垃ずなす。 発明の効果 かくの劂くしお䜜られた倚局構造の難燃性䞍織
垃は、すぐれた持続性のある難燃性を有し、しか
も、原反の柔軟性はそのたたであるので、凹凞板
材の衚面化粧材、熱成型物の衚面化粧材等の難燃
性が芁求され、しかも倉圢が容易でなければなら
ない分野に奜適に䜿甚される。 実斜䟋 以䞋実斜䟋を掲げお本発明を具䜓的に説明す
る。なお、䟋䞭の「郚」はこずわりのない限り重
量郚であり、「」はこずわりのない限り重量
である。 実斜䟋  粘床が1500センチポアズの40塩玠化された塩
玠化パラフむン東掋曹達補「トペパラツクス
A40」80郚、平均粒埄300メツシナのデカブロモ
ゞプニル゚ヌテル䞉井東圧補「プラネロン」
40郚、粉末グラフアむト日本黒鉛補「」
郚ず通垞のプロペラ匏撹拌機で混合均䞀化し、
粘床が2000センチポアズの安定な黒色の難燃性懞
濁液(F)を埗た。 䞀方、オルトクロルプノヌル䞭の極限粘床が
0.70であるポリ゚チレンテレフタレヌト70郚ず、
ポリプロピレン宇郚興産補「−115M」27
郚、黒のポリプロピレンマスタヌチツプ倧日粟
化補「PPM(F)ブラツク」郚及びタルク郚
をドラむブレンドしお、特公昭47−36833号の発
明の劂く、該ドラむブレンドチツプを溶融しお、
窒玠を吹蟌んで、抌し出し、ドラフトをかけお巻
き取り、巻き取り方向に無数の亀裂が入぀た䞍織
り゚ブを埗た。 この䞍織り゚ブを局重ねお、オヌバヌ
フむヌドし぀぀延展し、プレスした。あらかじめ
第局目の䞍織り゚ブに䞊蚘難燃化懞濁液(F)を第
局目の䞍織り゚ブ重量に察しお400付䞎せし
め、積局→オヌバヌフむヌド→延展→プレスの工
皋により、目付60m2、党䜓ずしお(F)の付着量
が60の䞍織垃−を埗た。 この䞍織垃−はそれ自身すぐれた撥氎
性ず難燃性を瀺し、䞍織垃䞭における難燃化懞濁
液(F)の移行、脱萜も少なか぀た。 次に䞊蚘䞍織垃−ず目付600m2の
綿を䞻䜓ずする、未硬化プノヌル暹脂を20含
んだプルト通称タカをmm厚に䞀䜓
熱成型した成型物を、䞊蚘䞍織垃−
偎を䞋面にしおJIS D1201の燃焌詊隓をする
ず、結果は「自消性」に該圓した。 たた䞊蚘䞍織垃−を画甚玙に10回こす
り぀けた埌、同様にタカに貌付しおも、
JIS D1201の結果は「自消性」であ぀た。たた画
甚玙ぞの難燃剀の移行もほずんどなか぀た。たた
グラフアむトの移行もなく、この䞍織垃は着色堅
牢性も優れおいた。 比范䟋 〜 衚に揚げる事項以倖は実斜䟋ず同様にしお
䜜぀た䞍織垃をそのたたタカず実斜䟋
ず同様の条件で䞀䜓熱成型したものの難燃性
JIS D1201、該䞍織垃を10回ほど画甚玙にこ
すり぀けた埌タカず䞀䜓熱成型したものの
難燃性JIS D1201難燃性の耐久評䟡、画
甚玙にこすり぀けた時の固䜓の脱萜床、液䜓の移
行床、倖䞍織垃の柔軟性に぀いお、実斜䟋の
䞍織垃−の評䟡結果ず䜵蚘しお衚に揚
げる。本発明の範囲から逞脱しおいるこれらの䞍
織垃は項目〜のいずれかが実斜䟋の䞍織垃
−に劣぀おいる。
[Industrial Application Field] The present invention relates to a novel flame-retardant nonwoven fabric. More specifically, the present invention relates to a nonwoven fabric that contains a specific flame-retardant suspension in the intermediate layer, has little release of the suspension, and has flexibility as a whole. [Prior Art] When the fiber material constituting the nonwoven fabric is nonflammable or flame retardant, such as an inorganic substance, wholly aromatic polyamide, polyvinyl chloride, or polyvinylidene chloride,
Although it can easily achieve the purpose of flame retardancy by itself,
Nonwoven fabrics made from synthetic fibers made from many other natural fibers, recycled fibers, polyamides other than fully aromatic polyamides, polyesters, polyolefins, and other synthetic polymers are not subjected to any flame retardant treatment. No flame retardant property is provided. For this reason, various methods have been proposed for making nonwoven fabric flame retardant. For example, there are a method of copolymerizing a flame retardant component, a method of kneading the component, a method of adhering the component, and the like. Of these, the method of attaching a flame retardant component is considered to be the simplest method to impart flame retardancy, but if the flame retardant is solid, it easily falls off, so it may not have an excellent flame retardant effect. However, its durability is poor and it cannot be applied to adhesion methods in many cases. On the other hand, if the flame retardant is a liquid, it is highly likely to migrate to other objects and cause contamination. In order to reduce these shedding, migration, and contamination, many methods are used to fix flame retardants to cloth or the like using a thermosetting binder. However, this method requires complicated steps, and the texture of the nonwoven fabric to be made flame retardant is impaired, resulting in poor flexibility. [Object of the invention] Therefore, the object of the present invention is to prevent the shedding, migration, and
An object of the present invention is to provide a flame-retardant nonwoven fabric that causes less contamination and less decrease in flexibility. [Structure of the Invention] The flame-retardant nonwoven fabric of the present invention has a viscosity of 0.02 to 100 poise, and contains 20 to 90% by weight of a nonvolatile liquid organic compound that does not substantially contain water, and a substantially A flame-retardant suspension formed by 80 to 10% by weight of a particulate solid flame-retardant substance that is insoluble in water and has an average particle size of less than 50 mesh is added to the entire non-woven fabric made of flame-retardant fibers. This is a flame-retardant nonwoven fabric in which an intermediate layer containing 5 to 100% by weight is interposed between upper and lower layers that do not contain a flame-retardant suspension, and all layers are integrated. In the particulate solid flame retardant material according to the present invention, "substantially insoluble" means that the solubility in the nonvolatile liquid-paired organic compound is 5% by weight or less. Furthermore, the term "non-volatile liquid organic compound" means an organic liquid having a vapor pressure of 1 mmHg or less at a temperature of 25°C. The average particle size of the particulate solid flame retardant material in the present invention is measured as follows. The solid is sampled on a slide, the particle size is measured, and the average is averaged. The average particle size (m) is calculated using the following formula, assuming that the average value is the sum of the values. (However, it shall be expressed in units of cm.) In that case, if the projection of the solid particle is not circular, the projected area (S) is measured for each sampled particle, and the radius (γ) of each particle is calculated as γ = √. It is assumed that the value is obtained by calculating the value using the formula and performing an arithmetic average of these γ's. The viscosity of the nonvolatile organic liquid used in the present invention was determined using a rotating cylinder viscometer, and was measured at a shear rate of 1/sec and a temperature of 25°C. If the viscosity is time-dependent, it refers to the viscosity after rotating the cylinder (rotor) for 30 minutes. The reason why a non-volatile organic liquid is used here is that if it is volatile, it will vaporize after being applied to the nonwoven fabric and the holding power of the solid flame retardant substance will be lost, making it impossible to achieve the purpose of the present invention. The flame retardant suspension in the present invention is formed from the nonvolatile organic liquid and the solid flame retardant substance, and it is sufficient that the solid flame retardant substance is at least flame retardant; The organic liquid may also have a flame retardant function, and there is no problem even if the two are combined to have a flame retardant function. These liquids and solids may be used alone or in a mixture of two or more. When the flame retardant suspension used in the present invention is included in a nonwoven fabric in a specific proportion, the flame retardant nonwoven fabric has extremely low liquid migration and solid shedding, and does not lose its original flexibility. can be obtained. Non-volatile liquid organic compounds have a viscosity of
0.02 to 100 poise, preferably 0.5 to 20 poise. If the viscosity is less than 0.02 poise,
The solid-liquid separation in the flame retardant suspension is severe, making it difficult to obtain a stable suspension, which not only makes it difficult to homogeneously apply the suspension to the nonwoven fabric, but also makes it more likely to fall off or migrate. . Furthermore, if a liquid with a strength exceeding 100 poise is used, it will be difficult to apply a flame retardant suspension using the liquid to the nonwoven fabric, and even if it is applied, it will lack uniformity and the nonwoven fabric will lose its flexibility. Specific examples of suitable liquid organic compounds include, for example, ethylene glycol, polyethylene glycol, liquid paraffin, polysiloxane, chlorinated paraffin, bromotrichloromethane, tetrabromoethane, 1,2-dibromo-1,1,2,2 −
Tetrachloroethane, tribromopropane, 1,
2-dibromo-3-chloropropane, tetrabromobutane, tris(2,3-dibromopropyl)
Phosphate, Tris(2-chloro-3-promopropyl)phosphate, Tris(2-bromo-
3-chloropropyl) phosphate and the like. Among these, the substances fried after chlorinated paraffin have flame retardant properties by themselves. On the other hand, solid flame retardant materials are those in the form of fine powders whose average particle size is less than 50 mesh. If the size is larger than 50 meshes, it is difficult to uniformly disperse it on the nonwoven fabric, and the co-retention ability with liquid is also reduced. Only particles with an average particle size smaller than 50 mesh can be uniformly dispersed and also have good co-retention with liquid organic compounds. Examples of such flame-retardant solids include inorganic compounds mainly containing oxides such as copper oxide, zinc oxide, tin oxide, silica, antimony trioxide, iron oxide, nickel oxide, and aluminum hydroxide; elements such as activated carbon, graphite), lead, iron; tetrabromo bisphenol A, carbonate oligomer of tetrabromo bisphenol A, tetrabromo bisphenol A derivatives; hexabromo benzene, decabromodiphenyl ether, tetrabromo phthalic anhydride, Examples include organic halogenated compounds having a flame retardant effect such as perchloropentacyclodecane. The flame retardant suspension of the present invention is formed from the liquid and solid, and its composition is such that the liquid is 20 to 90% by weight.
and the solids content is 80-10% by weight. The preferred composition is 30-80% liquid by weight and 70-80% solids.
20% by weight. It is more advantageous that the viscosity of the suspension is in the range of 0.1 to 200 poise, preferably 1 to 20 poise. If the amount of liquid in the flame retardant suspension exceeds 90% by weight, the retention of solids will be reduced and the liquid will migrate or fall off more easily, not only making it easier to contaminate other properties.
The flame retardancy of the nonwoven fabric also tends to decrease. On the other hand, if the proportion of the liquid is less than 20% by weight, the adhesion effect of the liquid to the solid will be reduced, and the migration and falling off of the solid will become noticeable, making it easier to contaminate other objects. may also decrease. The flame retardant suspension described above may contain small proportions of additives such as pigments and various stabilizers in addition to the liquids and solids described above. The flame retardant suspension is applied to the nonwoven fabric to be flame retardant (adhered nonwoven fabric) by 5 to 100% by weight, preferably
15-70% granted. If it is less than 5%, the nonwoven fabric will not be sufficiently flame retardant, and if it exceeds 100%, the original properties of the nonwoven fabric will be lost, and migration and shedding of the flame retardant suspension will become noticeable. . The flame retardant effect obtained by applying the flame retardant suspension of the present invention is most sustained when the flame retardant suspension is applied to the middle layer of a nonwoven fabric having a multilayer structure. The flame retardant suspension is easily applied to and incorporated into the web, which becomes the intermediate layer of the nonwoven fabric, by means such as rotating rolls, spraying, and bath dipping. Examples of effective methods for producing a flame-retardant nonwoven fabric with a multilayer structure include the following processes (a) to (c). (a) A flame retardant suspension specified in the present invention is applied to the web that will become the intermediate layer. (b) Upper and lower layers not coated with a flame retardant suspension are laminated on the intermediate layer. (c) The upper, middle, and lower layers are joined together by a process such as stretching and pressing or needle punching and pressing to form a nonwoven fabric. [Effects of the invention] The flame-retardant nonwoven fabric with a multilayer structure thus produced has excellent long-lasting flame retardancy, and the flexibility of the original fabric remains, so it can be used as a textured board material. It is suitably used in fields where flame retardancy is required, such as decorative surface materials for thermoformed products and materials that require easy deformation. [Examples] The present invention will be specifically described below with reference to Examples. In addition, "parts" in the examples are parts by weight unless otherwise specified, and "%" are percentages by weight unless otherwise specified.
It is. Example 1 A 40% chlorinated chlorinated paraffin with a viscosity of 1500 centipoise (“Toyoparax” manufactured by Toyo Soda)
A40) 80 parts, average particle size 300 mesh decabromodiphenyl ether (Mitsui Toatsu "Planeron")
40 parts, powder graphite (Nippon Graphite "P#2")
Mix 8 parts and homogenize with a normal propeller stirrer,
A stable black flame retardant suspension (F) with a viscosity of 2000 centipoise was obtained. On the other hand, the intrinsic viscosity of orthochlorophenol is
70 parts of polyethylene terephthalate, which is 0.70;
Polypropylene (“S-115M” manufactured by Ube Industries) 27
1 part, 3 parts of black polypropylene master chips ("PPM (F) 8 Black" manufactured by Dainichiseika Chemical Co., Ltd.) and 1 part of talc were dry blended, and the dry blend chips were melted as in the invention of Japanese Patent Publication No. 47-36833. do,
A nonwoven web (W) with numerous cracks in the winding direction was obtained by blowing nitrogen into it, extruding it, and winding it up under a draft. Eight layers of this nonwoven web (W) were stacked, spread while overfeeding, and pressed. The above flame retardant suspension (F) is applied in advance to the fourth layer nonwoven web at 400% of the weight of the fourth layer nonwoven web, and through the steps of lamination → overfeed → spreading → pressing, A nonwoven fabric (W-F) with a basis weight of 60 g/m 2 and an overall adhesion amount of (F) of 60% was obtained. This nonwoven fabric (W-F) itself exhibited excellent water repellency and flame retardancy, and there was little migration or shedding of the flame retardant suspension (F) in the nonwoven fabric. Next, the above nonwoven fabric (W-F) and felt (commonly known as Taka (T)), which is mainly made of cotton with a basis weight of 600 g/m 2 and contains 20% uncured phenol resin, are integrally thermoformed to a thickness of 4 mm ( S), the above nonwoven fabric (W-
When the JIS D1201 combustion test was conducted with the F) side facing down, the results were found to be "self-extinguishing." Also, if you rub the above nonwoven fabric (W-F) on drawing paper 10 times and then paste it on Taka (T) in the same way,
The result of JIS D1201 was "self-extinguishing". There was also almost no transfer of flame retardant to the drawing paper. Furthermore, there was no migration of graphite, and this nonwoven fabric had excellent color fastness. Comparative Examples 1 to 7 Nonwoven fabrics made in the same manner as in Example 1 except for the matters listed in Table 1 were used as Taka (T) and Example 1.
Flame retardant (JIS D1201) of the non-woven fabric integrally heat-molded under the same conditions as the non-woven fabric (JIS D1201), and flame retardant of the non-woven fabric integrally heat-molded with Taka (T) after rubbing it on drawing paper about 10 times (JIS D1201) (flame retardant) The evaluation results for the nonwoven fabric (W-F) of Example 1 are listed in Table 2 together with the evaluation results for the nonwoven fabric (W-F) of Example 1 regarding the degree of shedding of solids when rubbed against drawing paper, the degree of liquid migration, and the flexibility of the outer nonwoven fabric. These nonwoven fabrics that deviate from the scope of the present invention are inferior to the nonwoven fabric of Example 1 (W-F) in any of the following items.

【衚】【table】

【衚】 実斜䟋 〜 衚に揚げる事項以倖は実斜䟋ず同様にしお
䜜぀た䞍織垃を比范䟋〜ず同様にしお評䟡し
た結果は、実斜䟋の䞍織垃ずほずんど同じであ
぀た。
[Table] Examples 2 to 4 Nonwoven fabrics made in the same manner as in Example 1 except for the matters listed in Table 3 were evaluated in the same manner as in Comparative Examples 1 to 6. The results were almost the same as the nonwoven fabric of Example 1. Ta.

【衚】【table】

【衚】 実斜䟋  粘床150センチポアズの流動パラフむン関東
化孊補40郚、平均粒床300メツシナのデカブロ
モゞプニル゚ヌテル䞉井東圧補「プラネロ
ン」57郚、粉末グラフアむト日本黒鉛補「
」郚を通垞のプロペラ匏撹拌機で混合均
䞀化し、粘床が1100センチポアズの灰色の難燃性
懞濁液(F)を埗た。 この難燃性懞濁液(F)を、ポリ゚チレンテレフタ
レヌト延䌞トりを開繊しお埗た目付30m2の平
行䞍織垃(H)に25m2ほど付着せしめ、該䞍織垃
局を実斜䟋ず同様の成分で同様の方法により
補造した巻取り方向に無数の亀裂が入぀た目付20
m2の䞍織垃局の間に挿入しお、さら
に䞀面に目付31m2の特公昭47−36833号の劂
くしお補造したポリプロピレン100の亀裂䞍織
垃を局重ね合せた。 該積局物をオヌバヌフむヌドし぀぀延䌞−プレ
スしお目付65m2、厚さ125Όの難燃性䞍織垃
−を埗た。 該䞍織垃−は、それ自身すぐれた撥氎
性を瀺し、JIS D1201詊隓に斌お「自消性」を瀺
した。 次に、該䞍織垃−ず目付700m2の
未硬化プノヌル暹脂を20含んだガラス繊維マ
ツト(G)を、−のポリプロピレン100面を
ガラス繊維マツト偎に向けお、䞀䜓熱成型しお25
mm厚の成型物を埗た。該䞍織垃−
を䞋面にしおJIS D1201詊隓を行な぀た結果は
「自消性」ずいう刀定であ぀た。 実斜䟋  粘床ポアズのトリス−ゞクロロプロ
ピルホスプヌト50郚、平均粒埄500メツシナ
のタルク50郚を混合しお粘床50ポアズの難燃性懞
濁液(F)を埗た。該懞濁液(F)を目付30m2のポリ
゚ステル短繊維䞍織垃に15m2付着せし
めお、これを䞭間局ずし、該懞濁液を含たない䞊
䞋局ず積局・ニヌドルパンチを行぀お、べず぀き
のない難燃性䞍織垃−を埗た。 この䞍織垃−自身半氞久的な難燃性を
瀺し、実斜䟋及び実斜䟋のような他の基材ず
20Ό厚のポリ゚チレンを介しお䞀䜓熱成型した成
型物もJIS D1201に斌ける「自消性」を瀺した。 実斜䟋  メタクレゟヌル䞭の極限粘床が1.1であるポリ
−ε−カプロラクタム80郚、ポリプロピレン宇
郚興産補「TS−115M」10郚、オルトクロルフ
゚ノヌル䞭の極限粘床が0.55であるポリ゚チレン
テレフタレヌト10郚及びタルク郚をドラむブレ
ンドしお、特公昭47−36833号の劂くしお、亀裂
シヌトを埗た。該シヌトを䜿甚しお、実斜
䟋ず同じ工皋で同じ難燃剀をの総重量に察し
お50付着しお、目付60m2の難燃性䞍織垃
−を埗た。 次に該䞍織垃−ず目付600m2の綿
を䞻䜓ずする未硬化プノヌル暹脂を20含んだ
プルトをmm厚に䜓熱成型した成型物
はJIS D1201詊隓に斌お「自消性」であ぀た。 実斜䟋  実斜䟋に斌おデカブロモゞプニル゚ヌテル
の代りにテトラブロモ無氎フタヌル酞200メツ
シナを䜿甚する以倖は実斜䟋ずた぀たく同様
にしお補造した䞍織垃−はすぐれた耐久
性のある難燃性を瀺ししかも柔軟性も保持されお
いた。
[Table] Example 5 40 parts of liquid paraffin (manufactured by Kanto Kagaku) with a viscosity of 150 centipoise, 57 parts of decabromodiphenyl ether ("Planelon", manufactured by Mitsui Toatsu) with an average particle size of 300 mesh, powdered graphite ("Planelon", manufactured by Nippon Graphite), P
#2'') were mixed and homogenized using a conventional propeller-type stirrer to obtain a gray flame-retardant suspension (F) having a viscosity of 1100 centipoise. About 25 g/m 2 of this flame-retardant suspension (F) was attached to a parallel nonwoven fabric (H) with a basis weight of 30 g/m 2 obtained by opening stretched polyethylene terephthalate tow, and the two layers of the nonwoven fabric were used as examples. Fabric weight 20 with countless cracks in the winding direction manufactured by the same method with the same ingredients as 1.
It was inserted between five layers of non-woven fabric (W) with a weight of 31 g/m 2 and one layer of cracked non-woven fabric made of 100% polypropylene produced as in Japanese Patent Publication No. 47-36833 with a basis weight of 31 g/m 2 was superimposed on one side. Ta. The laminate was stretched and pressed while overfeeding to obtain a flame-retardant nonwoven fabric (WF) having a basis weight of 65 g/m 2 and a thickness of 125 ÎŒm. The nonwoven fabric (W-F) itself exhibited excellent water repellency and exhibited "self-extinguishing properties" in the JIS D1201 test. Next, the nonwoven fabric (W-F) and a glass fiber mat (G) containing 20% uncured phenolic resin with a basis weight of 700 g/m 2 were placed with the 100% polypropylene side of (W-F) facing the glass fiber mat. 25 by integrally heat molding the
A molded article (S) with a thickness of mm was obtained. The nonwoven fabric (W-F)
The JIS D1201 test was conducted with the material facing down, and the result was that it was "self-extinguishing." Example 6 50 parts of tris(2,3-dichloropropyl) phosphate having a viscosity of 2 poise and 50 parts of talc having an average particle size of 500 mesh were mixed to obtain a flame retardant suspension (F) having a viscosity of 50 poise. The suspension (F) was applied at 15 g/m 2 to a polyester short fiber non-woven fabric (W) having a basis weight of 30 g/m 2 and used as an intermediate layer, which was laminated and needle-punched with the upper and lower layers not containing the suspension. A flame-retardant nonwoven fabric (WF) without stickiness was obtained. This nonwoven fabric (W-F) itself exhibits semi-permanent flame retardancy, and can be used with other base materials such as Example 1 and Example 2.
The molded product, which was integrally thermoformed using 20ÎŒ thick polyethylene, also exhibited "self-extinguishing properties" according to JIS D1201. Example 7 80 parts of poly-ε-caprolactam with an intrinsic viscosity of 1.1 in metacresol, 10 parts of polypropylene (“TS-115M” manufactured by Ube Industries), and 10 parts of polyethylene terephthalate with an intrinsic viscosity of 0.55 in orthochlorophenol. and 2 parts of talc were dry blended to obtain a cracked sheet (W) as described in Japanese Patent Publication No. 47-36833. Using this sheet, the same flame retardant was applied in an amount of 50% based on the total weight of W in the same process as in Example 1 to obtain a flame retardant nonwoven fabric (WF) with a basis weight of 60 g/m 2 . Next, the nonwoven fabric (W-F) and a felt containing 20% uncured phenolic resin, which is mainly cotton with a basis weight of 600 g/m 2 , were thermoformed into a 4 mm thick molded product (S).
was "self-extinguishing" in the JIS D1201 test. Example 8 A nonwoven fabric (W-F) produced in exactly the same manner as in Example 1 except that tetrabromo phthalic anhydride (200 mesh) was used instead of decabromodiphenyl ether was excellent. It exhibited durable flame retardancy and retained flexibility.

Claims (1)

【特蚱請求の範囲】[Claims]  粘床が0.02〜100ポアズでありか぀実質的に
氎を含たない䞍揮発性の液䜓状有機化合物20〜90
重量ず該液䜓に察し実質的に䞍溶性であり平均
粒埄が50メツシナより小さい埄の埮粒子状固䜓難
燃性物質80〜10重量ずより圢成される難燃化懞
濁液を非難燃性繊維からなる䞍織垃党䜓に察しお
〜100重量に盞圓する量包含せしめた䞭間局
を、難燃化懞濁液を含たない䞊䞋局の間に介圚せ
しめ党局を結合しおなる難燃性䞍織垃。
1 Nonvolatile liquid organic compound with a viscosity of 0.02 to 100 poise and substantially free of water 20 to 90
% by weight and 80 to 10% by weight of a particulate solid flame retardant material that is substantially insoluble in the liquid and has an average particle size smaller than 50 mesh. A flame-retardant material in which an intermediate layer containing 5 to 100% by weight of the entire nonwoven fabric made of fibers is interposed between upper and lower layers that do not contain a flame-retardant suspension, and all layers are bonded together. Non-woven fabric.
JP216379A 1979-01-16 1979-01-16 Fire retardant nonwoven fabric Granted JPS5598954A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP216379A JPS5598954A (en) 1979-01-16 1979-01-16 Fire retardant nonwoven fabric
US06/051,742 US4242398A (en) 1979-01-16 1979-06-25 Fibrous shaped article having non-level surface
DE7979301237T DE2963930D1 (en) 1979-01-16 1979-06-26 Fibrous shaped article, process for producing said article, and use of said article as soundproofing or heat insulating material for buildings
EP79301237A EP0013468B1 (en) 1979-01-16 1979-06-26 Fibrous shaped article, process for producing said article, and use of said article as soundproofing or heat insulating material for buildings

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP216379A JPS5598954A (en) 1979-01-16 1979-01-16 Fire retardant nonwoven fabric

Publications (2)

Publication Number Publication Date
JPS5598954A JPS5598954A (en) 1980-07-28
JPS6357540B2 true JPS6357540B2 (en) 1988-11-11

Family

ID=11521682

Family Applications (1)

Application Number Title Priority Date Filing Date
JP216379A Granted JPS5598954A (en) 1979-01-16 1979-01-16 Fire retardant nonwoven fabric

Country Status (1)

Country Link
JP (1) JPS5598954A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0357645U (en) * 1989-10-06 1991-06-04

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5526300A (en) * 1978-08-16 1980-02-25 Velsicol Chemical Corp Fire retardant nonwoven material

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5526300A (en) * 1978-08-16 1980-02-25 Velsicol Chemical Corp Fire retardant nonwoven material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0357645U (en) * 1989-10-06 1991-06-04

Also Published As

Publication number Publication date
JPS5598954A (en) 1980-07-28

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