JPS63309645A - Interior material of airplane - Google Patents
Interior material of airplaneInfo
- Publication number
- JPS63309645A JPS63309645A JP62142759A JP14275987A JPS63309645A JP S63309645 A JPS63309645 A JP S63309645A JP 62142759 A JP62142759 A JP 62142759A JP 14275987 A JP14275987 A JP 14275987A JP S63309645 A JPS63309645 A JP S63309645A
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- flame
- sulfur
- fiber
- resistant
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims description 28
- 239000000835 fiber Substances 0.000 claims description 49
- 229910052717 sulfur Inorganic materials 0.000 claims description 23
- 239000011593 sulfur Substances 0.000 claims description 23
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 21
- 239000004744 fabric Substances 0.000 claims description 18
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
- 230000000903 blocking effect Effects 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 229920002972 Acrylic fiber Polymers 0.000 description 12
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000004760 aramid Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 229920003235 aromatic polyamide Polymers 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- 229920000049 Carbon (fiber) Polymers 0.000 description 5
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
- 239000004917 carbon fiber Substances 0.000 description 5
- 239000003063 flame retardant Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 4
- 238000009940 knitting Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000004745 nonwoven fabric Substances 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 3
- 229920006231 aramid fiber Polymers 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 230000015271 coagulation Effects 0.000 description 3
- 238000005345 coagulation Methods 0.000 description 3
- 238000000578 dry spinning Methods 0.000 description 3
- -1 hydroxyalkyl acrylates Chemical class 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 238000005987 sulfurization reaction Methods 0.000 description 3
- 238000002166 wet spinning Methods 0.000 description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 description 2
- 229920005830 Polyurethane Foam Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 description 2
- 239000011496 polyurethane foam Substances 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 description 1
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OYUNTGBISCIYPW-UHFFFAOYSA-N 2-chloroprop-2-enenitrile Chemical compound ClC(=C)C#N OYUNTGBISCIYPW-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 1
- NJMYQRVWBCSLEU-UHFFFAOYSA-N 4-hydroxy-2-methylidenebutanoic acid Chemical compound OCCC(=C)C(O)=O NJMYQRVWBCSLEU-UHFFFAOYSA-N 0.000 description 1
- 206010000369 Accident Diseases 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920000784 Nomex Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229920001494 Technora Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 229920006240 drawn fiber Polymers 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000004763 nomex Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005486 sulfidation Methods 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000004950 technora Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Landscapes
- Inorganic Fibers (AREA)
- Woven Fabrics (AREA)
- Fireproofing Substances (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、ファイヤーブロッキング性(耐防火性〉に優
れた航空機内装材に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an aircraft interior material with excellent fire blocking properties (fire resistance).
(従来の技術)
近年、航空機の火災事故を契機に内装材の難燃化規制が
年々厳しくなりつつある。従って航空機の座席、壁、天
井および床などの内装材には火災から人命を守るため種
々の防火材すなわちファイヤーブロッキング材が使用さ
れている。例えば、座席の表地と内部のポリウレタンフ
ォームとの間にファイヤーブロッキングレイヤーと呼ば
れる耐炎布が配置されている。(Prior Art) In recent years, regulations on making interior materials flame retardant have become stricter year by year, triggered by aircraft fire accidents. Therefore, various fire-retardant materials, ie, fire-blocking materials, are used for interior materials such as seats, walls, ceilings, and floors of aircraft in order to protect human lives from fires. For example, a flame-resistant fabric called a fire blocking layer is placed between the outer material of the seat and the polyurethane foam inside.
ところで、上記ファイヤーブロッキングレイヤーとして
は、これまで種々の素材が提案されてきた。例えば、特
開昭61−55268号公報には、アクリル系繊維を空
気中で加熱、酸化した耐炎化繊維(セミカーボン繊維)
とパラ配向芳香族ポリアミド繊維からなる布帛にシリコ
ーン樹脂をコーティングした耐炎加工布が開示されてい
る。By the way, various materials have been proposed for the fire blocking layer. For example, in JP-A No. 61-55268, flame-resistant fibers (semi-carbon fibers) are made by heating and oxidizing acrylic fibers in the air.
A flame-resistant fabric is disclosed in which a fabric made of para-oriented aromatic polyamide fibers is coated with a silicone resin.
しかし、アクリル系繊維を高温の空気中で加熱、酸化す
ることによって製造される耐炎化繊維は、繊維の内部に
比較して繊維の表皮部の酸化の程度が極めて大きい不均
一な酸化構造を有しているために、機械的強度、特に引
張強度が小さく、靭性(タフネス)が低く、紡績または
編織が困難であり、仮に紡編織し得たとしても、jqら
れだ布帛は耐摩耗性に劣り、満足すべきものではなかっ
た。However, flame-resistant fibers produced by heating and oxidizing acrylic fibers in high-temperature air have a non-uniform oxidation structure in which the surface area of the fibers is extremely oxidized compared to the inside of the fibers. Because of this, it has low mechanical strength, especially tensile strength, and low toughness, making spinning or knitting difficult. , was not satisfactory.
そのため、上記のごとくパラ配向芳香族ポリアミド繊維
を多量に併用し耐摩耗性の改善をはかることになるが、
このパラ配向芳香族ポリアミド繊維を多く使用すると布
帛の難燃性が低下するといつた問題があった。Therefore, as mentioned above, large amounts of para-oriented aromatic polyamide fibers are used in combination to improve wear resistance.
There is a problem in that when a large amount of this para-oriented aromatic polyamide fiber is used, the flame retardance of the fabric decreases.
一方、航空機の壁、天井および床はメタ系アラミド繊維
のハニカムにガラス繊維、カーボン繊維あるいはパラ系
アラミド繊維などの布帛からなるFRPを積層した構造
になっているが、ファイヤーブロッキング材としてはそ
れぞれ一長一短があり必ずしも十分なものではない。例
えば、ガラス繊維は重い、カーボン繊維は高価およびパ
ラ系アラミド繊維は難燃性不足などといったそれぞれ問
題があり、特にパラ系アラミド繊維は今後の厳しい難燃
化規制を満足するのは困難でおる。On the other hand, the walls, ceilings, and floors of aircraft are constructed by laminating FRP made of fabrics such as glass fiber, carbon fiber, or para-aramid fiber on a honeycomb of meta-aramid fibers, but each has its own merits and demerits as a fire-blocking material. However, it is not always sufficient. For example, glass fibers are heavy, carbon fibers are expensive, and para-aramid fibers lack flame retardancy.In particular, it will be difficult for para-aramid fibers to meet future strict flame retardant regulations.
(発明が解決しようとする問題点)
本発明の目的は、引張強度が高く、靭性(タフネス)お
よび難燃性に優れた硫黄含有アクリル系耐炎化繊維の布
帛をファイヤーブロッキング材とすることによって、高
強力で耐摩耗性に優れ、かつ軽量で安価な航空機内装材
を提供することにある。(Problems to be Solved by the Invention) An object of the present invention is to use a sulfur-containing acrylic flame-resistant fiber fabric with high tensile strength, excellent toughness, and flame retardancy as a fire blocking material. The purpose of the present invention is to provide an aircraft interior material that is highly strong, has excellent wear resistance, is lightweight, and is inexpensive.
(問題点を解決するための手段)
このような本発明の目的は、前記特許請求の範囲に記載
したように、引張強度が少なくとも3゜5g/d、限界
酸素指数(LOI)が40以上および硫黄含有量が5重
量%以上である硫黄含有アクリル系耐炎化繊維の布帛を
ファイヤーブロッキング材として構成した航空機内装材
によって達成することができる。(Means for Solving the Problems) As described in the claims, the object of the present invention is to have a tensile strength of at least 3°5 g/d, a limiting oxygen index (LOI) of 40 or more, and This can be achieved by using an aircraft interior material made of a sulfur-containing acrylic flame-resistant fiber fabric having a sulfur content of 5% by weight or more as a fire blocking material.
本発明の航空機内装材を構成する硫黄含有アクリル系耐
炎化繊維は(以下、単に耐炎化繊維という)、その難燃
性が酸素結合の導入によるものではなくて、硫黄結合の
導入に基因する点に特徴かあり、かつその硫黄含有量が
5重量%以上、好ましくは8〜25重耐%であって、難
燃性の程度を表す限界酸素指数(LOI)が40以上、
好ましくは45〜70および引張強度が少なくとも3゜
5g/d、好ましくは4〜9g/dであることが必要で
ある。そして、上記硫黄含有アクリル系耐炎化繊維によ
り優れた加工性と耐摩耗性を付与する上で、該耐炎化繊
維は引張強度(g/d)と引張伸度(%)の平方根との
積で表わされる靭性(タフネス)は、10以上、好まし
くは12〜35であることが望ましい。The sulfur-containing acrylic flame-resistant fiber (hereinafter simply referred to as flame-resistant fiber) constituting the aircraft interior material of the present invention has a flame retardancy that is not due to the introduction of oxygen bonds but to the introduction of sulfur bonds. and has a sulfur content of 5% by weight or more, preferably 8 to 25% by weight, and a limiting oxygen index (LOI) representing the degree of flame retardancy of 40 or more,
45-70 and a tensile strength of at least 3.5 g/d, preferably 4-9 g/d. In order to impart superior processability and wear resistance to the sulfur-containing acrylic flame-resistant fiber, the flame-resistant fiber has a It is desirable that the displayed toughness is 10 or more, preferably 12 to 35.
ここで、硫黄の含有量が5重量%よりも少ないと、難燃
性のみならず、耐熱性や耐薬品性などの特性を十分に付
与できなくなるし、また余りに多くなると機械的強度が
低下するので好ましくない。If the sulfur content is less than 5% by weight, it will not be possible to provide sufficient properties such as flame retardancy, heat resistance, and chemical resistance, and if it is too large, mechanical strength will decrease. So I don't like it.
さらに、引張強度が3.5g/dよりも小さい場合は、
該耐炎化繊維を紡績、編iおよびニードルパンチなどに
よって糸条物や布帛などに転換する際に、風綿が発生し
易く、良好な糸条物や布帛などの製品を得ることができ
ないし、またファイヤーブロッキングレイヤーとして使
用中に繊維が摩耗、脱落し、耐久性に乏しいものとなり
、実用性を満足しないのである。Furthermore, if the tensile strength is less than 3.5 g/d,
When the flame-resistant fibers are converted into yarns, fabrics, etc. by spinning, knitting, needle punching, etc., fluff is likely to occur, making it impossible to obtain good yarns, fabrics, and other products. Furthermore, during use as a fire blocking layer, the fibers wear out and fall off, resulting in poor durability and unsatisfactory practicality.
本発明に用いる引張強度が少なくとも3.5g/d、L
OIが40以上および硫黄含有量が5重量%以上である
耐炎化繊維は、以下に詳述する特定のアクリル系繊維を
使用し、かつ特定の硫化工程および条件を採用すること
によってはじめて得ることができる。The tensile strength used in the present invention is at least 3.5 g/d, L
Flame-resistant fibers with an OI of 40 or more and a sulfur content of 5% by weight or more can only be obtained by using specific acrylic fibers and by adopting specific sulfiding processes and conditions as detailed below. can.
すなわち、まずアクリル系繊維としては、その重合度が
極限粘度で少なくとも1.5、好ましくは2.0〜5.
0の高重合度ポリマを使用し、このような高重合度ポリ
マからできる限り高強度、高弾性率のアクリル系繊維、
すなわち引張強度が少なくとも7g/d、好ましくは9
y/d以上さらに好ましくは10g/d以上のアクリル
系繊維を形成させることが必要である。That is, first, the degree of polymerization of the acrylic fiber is at least 1.5 in terms of intrinsic viscosity, preferably 2.0 to 5.
Acrylic fibers with as high strength and high modulus as possible from such high polymerization degree polymers are used.
i.e. a tensile strength of at least 7 g/d, preferably 9
It is necessary to form acrylic fibers of y/d or more, more preferably 10 g/d or more.
モして耐炎化繊維は、該アクリル系繊維を硫黄含有雰囲
気中で比較的緩慢な反応条件下に加熱、硫化し、繊維内
部まで十分に硫黄結合を導入し、内外構造差の少ない耐
炎化繊維とすることが必要であるが、このような内外構
造差の少ない高強度耐炎化繊維の製造には、アクリル系
繊維としても内外構造差が小さく、緻密で高強度である
ことが要求されるのである。Flame-resistant fibers are produced by heating and sulfurizing the acrylic fibers in a sulfur-containing atmosphere under relatively slow reaction conditions to fully introduce sulfur bonds into the fibers, resulting in flame-resistant fibers with little difference in internal and external structure. However, in order to manufacture such high-strength flame-resistant fibers with small differences in internal and external structures, acrylic fibers are required to have small differences in internal and external structures, be dense, and have high strength. be.
ここで、前記本発明に使用されるアクリル系繊維を構成
するアクリロニトリル(以下ANと略す)系重合体とし
ては、AN単独ポリマまたは、共重合成分としてアクリ
ル酸、メタクリル酸、イタコン酸などカルボン酸および
それらの低級アルキルエステル類、ヒドロキシエチルア
クリレート、ヒドロキシエチルメタアクリレートなどの
カルボン震の水酸基を含有するヒドロキシアルキルアク
リレート、アクリルアミド、メタクリルアミド、α−ク
ロルアクリロニトリル、ヒドロキシエチルアクリル酸、
アワルスルホン酸、メタクリルスルホン酸などを例示す
ることができるが、これらの中で硫化反応か速く、引張
強度の高い耐炎化繊維が得られるアクリルアミド類が特
に好ましく、その共重合量は10モル%以下、好ましく
は1〜7モル%である。Here, the acrylonitrile (hereinafter abbreviated as AN)-based polymer constituting the acrylic fiber used in the present invention may be an AN sole polymer or a carboxylic acid such as acrylic acid, methacrylic acid, itaconic acid, etc. as a copolymer component. Lower alkyl esters thereof, hydroxyalkyl acrylates containing a carboxyl hydroxyl group such as hydroxyethyl acrylate, hydroxyethyl methacrylate, acrylamide, methacrylamide, α-chloroacrylonitrile, hydroxyethyl acrylic acid,
Examples include awalsulfonic acid and methacrylsulfonic acid, but among these, acrylamides are particularly preferred because they undergo a quick sulfurization reaction and produce flame-resistant fibers with high tensile strength, and their copolymerization amount is 10 mol% or less. , preferably 1 to 7 mol%.
これらのAN系ポリマは、その溶剤、たとえばジメチル
スルホキシド(DMSO) 、ジメチルアセタミド(D
MAc>、ジメチルホルムアミド(DMF>などの有機
溶剤、塩化カルシウム、塩化亜鉛、ロダンソーダなどの
無機塩濃厚水溶液、硝酸などの無機系溶剤に、好ましく
はDMSOなどの有機溶剤に溶解して、ポリマ濃度が5
〜20%の紡糸原液とされる。These AN-based polymers can be used in their solvents, such as dimethyl sulfoxide (DMSO), dimethyl acetamide (D
MAc>, dimethylformamide (DMF>, etc.), a concentrated aqueous solution of an inorganic salt such as calcium chloride, zinc chloride, Rodan soda, etc., an inorganic solvent such as nitric acid, preferably an organic solvent such as DMSO, to increase the polymer concentration. 5
~20% spinning dope.
そして得られた紡糸原液の紡糸方法としては、該高重合
度のAN系ポリマから高強度、高弾性率の内外構造差の
小さい、緻密なアクリル系繊維を製造する上で、乾・湿
式紡糸、すなわち紡糸口金面と凝固浴液面との間の距離
を1〜20m、好ましくは3〜10mの範囲内に設定し
、該紡糸口金孔から紡糸口金面と凝固浴液面とで形成さ
れる微小空間に紡糸原液を吐出した後、凝固浴に導き凝
固させる方法を採用し、次いで得られた凝固繊維糸条を
常法により、水洗、脱溶媒、1次延伸、乾燥・緻密化、
2次延伸、熱処理などのあと処理工程を経由せしめて延
伸繊維糸条とする。この乾・湿式紡糸によって得られる
繊維糸条は、延伸性に極めて優れているが、好ましくは
2次延伸方法として、150〜270’Cの乾熱下に少
なくとも1゜1倍、好ましくは1.5倍以上延伸し、全
有効延伸倍率が少なくとも10倍、好ましくは12倍以
上になるように延伸し、その繊度を0.5〜7デニール
(d)、好ましくは1〜5dの範囲内にするのがよい。The spinning method of the obtained spinning dope includes dry/wet spinning, dry spinning, wet spinning, That is, the distance between the spinneret surface and the coagulation bath liquid level is set within the range of 1 to 20 m, preferably 3 to 10 m, and the microscopic particles formed by the spinneret surface and the coagulation bath liquid surface are separated from the spinneret hole. After discharging the spinning stock solution into the space, a method is adopted in which it is introduced into a coagulation bath and coagulated, and then the obtained coagulated fiber thread is washed with water, desolventized, primary stretched, dried and densified, and then subjected to conventional methods.
The fibers are subjected to post-processing steps such as secondary drawing and heat treatment to form drawn fiber threads. The fiber yarn obtained by this dry/wet spinning has extremely excellent drawability, but preferably the secondary drawing method is at least 1.1 times, preferably 1. Stretched 5 times or more so that the total effective stretching ratio is at least 10 times, preferably 12 times or more, and the fineness is in the range of 0.5 to 7 denier (d), preferably 1 to 5 d. It is better.
この繊度が0.5dよりも小さいと、得られる耐炎化繊
維の紡績性が低下し、耐摩耗性の良好な繊維製品を得る
ことが難しくなるし、7dよりも大きいと、硫化処理時
の繊維断面における硫化が不均一になるために好ましく
ない。If the fineness is smaller than 0.5d, the spinnability of the resulting flame-resistant fiber will be reduced, making it difficult to obtain textile products with good abrasion resistance.If the fineness is larger than 7d, the fiber during sulfurization will This is not preferable because sulfidation becomes uneven in the cross section.
かくして得られたアクリル系繊維は、硫黄含有雰囲気、
たとえば二硫化炭素、硫化水素、二酸化硫黄および硫黄
ガスなどの単独または混合ガス中で加熱、耐炎化される
が、好ましくは繊維断面全体が均一に硫化された(二重
構造でない)繊維を再現性よく)qることができる二酸
化硫黄を硫黄含有雰囲気として使用するのがよい。また
耐炎化温度は230〜400’Cの温度領域で加熱、硫
化するのがよい。The acrylic fiber thus obtained is exposed to a sulfur-containing atmosphere,
For example, the fibers are flame-proofed by heating in single or mixed gases such as carbon disulfide, hydrogen sulfide, sulfur dioxide, and sulfur gas, but preferably the fibers are uniformly sulfurized (not double-layered) over the entire fiber cross section. It is preferable to use sulfur dioxide as the sulfur-containing atmosphere. Further, it is preferable to heat and sulfurize the flameproofing temperature in a temperature range of 230 to 400'C.
すなわち本発明者らの検討によれば、この二酸化硫黄雰
囲気中で上記アクリル系繊維を加熱、硫化する場合には
、耐炎化反応が通常の空気などの酸化性雰囲気での酸化
反応に比較して緩慢であり、二酸化硫黄が繊維中にスム
ースに浸透し、結果として硫黄原子が繊維断面全体に均
−分イ[シた、内外構造差のない繊維WI造を有する耐
炎化繊維にすることかできるので有利である。In other words, according to the studies of the present inventors, when the acrylic fibers are heated and sulfurized in this sulfur dioxide atmosphere, the flame resistance reaction is faster than the oxidation reaction in an oxidizing atmosphere such as ordinary air. Sulfur dioxide penetrates smoothly into the fiber, and as a result, sulfur atoms are distributed evenly over the entire cross section of the fiber, making it possible to create a flame-resistant fiber with a fiber WI structure with no difference between the inner and outer structures. Therefore, it is advantageous.
なあ、本発明において、硫黄含有雰囲気、特に二酸化硫
黄雰囲気には、窒素、酸素などの他のカスを滋宜混合し
た加熱雰囲気であってもよく、特に二酸化硫黄と窒素と
の混合ガスは、二酸化硫黄を効率良く、繊維と反応させ
る上で有効でおる。Incidentally, in the present invention, the sulfur-containing atmosphere, especially the sulfur dioxide atmosphere, may be a heated atmosphere in which other gases such as nitrogen and oxygen are mixed together. In particular, the mixed gas of sulfur dioxide and nitrogen is It is effective in efficiently reacting sulfur with fibers.
この耐炎化工程の加熱は、一定温度条件下でもよいし、
昇温下でもよく、またアクリル系繊維は緊張、定長また
は弛緩のいずれの条件下でもよい。The heating in this flameproofing step may be performed under constant temperature conditions,
The temperature may be elevated, and the acrylic fibers may be under tension, constant length, or relaxation.
1例として、第1段加熱を230〜280’Cの温度範
囲に保たれた加熱炉中で行い、第2段加熱を280〜4
00 ’Cの温度範囲内で、かつ段階的に昇温条件に設
定された加熱炉中で硫化を完結させる方法を挙げること
ができる。As an example, the first stage heating is carried out in a heating furnace maintained at a temperature range of 230-280'C, and the second stage heating is carried out at a temperature range of 280-440'C.
One example is a method in which sulfurization is completed within a temperature range of 00'C in a heating furnace set to temperature increasing conditions in stages.
次に本発明の航空機内装材を開成する布帛は、上記耐炎
化繊維を用いて通常の方法によって一45帛化される。Next, the fabric constituting the aircraft interior material of the present invention is made into a 145-woven fabric using the above-mentioned flame-resistant fibers by a conventional method.
たとえば、耐炎化繊維からなるフィラメントヤーンまた
は紡績糸を製織または製編する方法によって容易に布帛
化することかできる。また、該耐炎化繊維のステープル
にニードルパンチを施すことによってjqられる不織布
であってもよい。For example, it can be easily made into a fabric by weaving or knitting filament yarns or spun yarns made of flame-resistant fibers. Alternatively, it may be a nonwoven fabric that is formed by needle punching a staple of the flame-resistant fiber.
これらの製編、製織および不i布製造に際して、より高
い引張強度と耐摩耗性を付与するため“′ビニロンパ、
アラミド繊維(たとえば“ケブラーパ、“テクノーラ゛
および″ノーメックス″など)、ポリフェニレンサルフ
ァイド(PPS)繊維、ポリイミド繊維、フェノール織
組、綿、羊毛、無殿系繊維などを混繊、混紡または混撚
し、用途に適した製品性能を与えることができる。In order to provide higher tensile strength and abrasion resistance during knitting, weaving, and non-woven fabric production,
Aramid fibers (e.g. Kevlarpa, Technora and Nomex), polyphenylene sulfide (PPS) fibers, polyimide fibers, phenolic weave, cotton, wool, non-woven fibers, etc. are blended, spun or mixed and twisted for various purposes. can provide product performance suitable for
また、より高度なファイヤーブロッキング性を付与する
ため、上記布帛に難燃性の樹脂やゴムを含浸、又はコー
ティングすることもできる。Furthermore, in order to impart higher fire-blocking properties, the fabric may be impregnated with or coated with a flame-retardant resin or rubber.
次に、本発明の航空機内装材の例を図面に基づき具体的
に説明する。Next, examples of the aircraft interior material of the present invention will be specifically explained based on the drawings.
第1図は、本発明に係る航空機内装材の一実施態様であ
る座席の断面図で、座席シートの表地1とポリウレタン
フォーム2の間にファイヤーブロッキングレイヤーとし
て硫黄含有アクリル系耐炎化繊維からなる不織布3を配
置したものである。FIG. 1 is a cross-sectional view of a seat that is an embodiment of the aircraft interior material according to the present invention, in which a nonwoven fabric made of sulfur-containing acrylic flame-resistant fiber is used as a fire blocking layer between the outer material 1 and the polyurethane foam 2 of the seat. 3 is arranged.
第2図は本発明に係る航空機内装材の一実施態様である
壁あるいは天井の断面図で、メタ系アラミド繊維のハニ
カム4の前後にカーボン繊維のフィラメントの織物5お
よびその上側に7フイヤーブロツキング材として硫黄含
有アクリル系耐炎化繊維のフィラメント織物6を配置し
、フェノール樹脂7で接合し、その表面に塗装置を施し
たものである。 なお、本発明において、限界酸素指数
(LOI)および引張強度は次の測定法により測定した
値である。FIG. 2 is a cross-sectional view of a wall or ceiling that is an embodiment of the aircraft interior material according to the present invention, in which a carbon fiber filament fabric 5 is placed before and after a honeycomb 4 made of meta-aramid fibers, and 7 fiber blocks are placed above the honeycomb 4. A filament fabric 6 of sulfur-containing acrylic flame-resistant fiber is arranged as a packing material, bonded with a phenol resin 7, and its surface is coated. In the present invention, the limiting oxygen index (LOI) and tensile strength are values measured by the following measuring method.
限界酸素指数(LOI):
J Is−に−7201に規定されている測定法に準じ
て測定される値であり、ざらに具体的には次の通り。Limiting Oxygen Index (LOI): A value measured according to the measurement method specified in JIS-7201, and the specific details are as follows.
測定試料的1gを直径約1mの針金(支持体)に巻付け
、直径が約4#の紐状にしてタテ150mの枠に固定す
る。次いでこれを燃焼筒内にセットし、その中に酸素と
窒素の混合ガスを11.41/minの流速で約30秒
間流した後、試料の上端に点火し、試料が3分間以上燃
焼し続けるかまたは着火した後、50#I#I以上の燃
焼長まで燃え続けるのに必要な最低の酸素流量(A)と
、その時の窒素流1(B)とを決定する。その混合ガス
の総流量に対する酸素流量の割合がLOfであり、次式
によって示される。Wrap 1 g of the sample to be measured around a wire (support) with a diameter of about 1 m, form a string with a diameter of about 4#, and fix it to a frame with a length of 150 m. Next, this is set in a combustion cylinder, and after flowing a mixed gas of oxygen and nitrogen into it at a flow rate of 11.41/min for about 30 seconds, the upper end of the sample is ignited, and the sample continues to burn for more than 3 minutes. Or, after ignition, determine the minimum oxygen flow rate (A) necessary to continue burning to a combustion length of 50#I#I or more, and the nitrogen flow rate 1 (B) at that time. The ratio of the oxygen flow rate to the total flow rate of the mixed gas is LOf, which is expressed by the following equation.
LOI= (A/ (A十B>)x100引張強度:
J l5−L−1069に規定されている測定法に準じ
て測定した。LOI=(A/(A+B>)×100 Tensile strength: Measured according to the measuring method specified in J15-L-1069.
(発明の効果〉
本発明に係る航空機内装材は、繊維断面方向に均一に硫
化され、高強度でかつ難燃性に優れた硫黄含有アクリル
系耐炎化繊維からなる布帛をファイヤーブロッキング材
としてるから、ファイヤーブロッキング性に優れている
のみならず、耐摩耗性などの機械的性質にも優れている
ので、年々厳しくなる航空機内装材の難燃化規制に対し
、十分対応ができる。しかも、上記布帛は安価で軽ωで
あるため航空機用途に極めて有用である。(Effects of the Invention) The aircraft interior material according to the present invention uses, as a fire blocking material, a fabric made of sulfur-containing acrylic flame-resistant fibers that are uniformly sulfurized in the cross-sectional direction of the fibers and have high strength and excellent flame retardancy. Not only does it have excellent fire blocking properties, but it also has excellent mechanical properties such as abrasion resistance, so it can fully comply with the flame retardant regulations for aircraft interior materials that are becoming stricter every year. is inexpensive and lightweight, making it extremely useful for aircraft applications.
第1図は本発明に係る航空機内装材の一実施態様である
座席の断面図、第2図は本発明に係る航空機内装材の一
実施態様である壁あるいは天井の断面図である。
1:表地
2:ウレタンフオーム
3:硫黄含有アクリル系耐炎化繊維の不織布4:ハニカ
ム
5:カーボン繊維のフィラメント織物
6:硫黄含有アクリル系耐炎化繊維のフィラメント織物
7:フェノール樹脂
8:塗料FIG. 1 is a cross-sectional view of a seat, which is an embodiment of the aircraft interior material according to the present invention, and FIG. 2 is a cross-sectional view of a wall or ceiling, which is an embodiment of the aircraft interior material according to the present invention. 1: Outer material 2: Urethane foam 3: Nonwoven fabric of sulfur-containing acrylic flame-resistant fiber 4: Honeycomb 5: Filament fabric of carbon fiber 6: Filament fabric of sulfur-containing acrylic flame-resistant fiber 7: Phenol resin 8: Paint
Claims (1)
数(LOI)が40以上および硫黄含有量が5重量%以
上である硫黄含有アクリル系耐炎化繊維の布帛をファイ
ヤーブロッキング材として構成したことを特徴とする航
空機内装材。(1) The fire blocking material is composed of a sulfur-containing acrylic flame-resistant fiber fabric having a tensile strength of at least 3.5 g/d, a limiting oxygen index (LOI) of 40 or more, and a sulfur content of 5% by weight or more. Aircraft interior materials featuring:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62142759A JPS63309645A (en) | 1987-06-08 | 1987-06-08 | Interior material of airplane |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62142759A JPS63309645A (en) | 1987-06-08 | 1987-06-08 | Interior material of airplane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS63309645A true JPS63309645A (en) | 1988-12-16 |
Family
ID=15322915
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62142759A Pending JPS63309645A (en) | 1987-06-08 | 1987-06-08 | Interior material of airplane |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63309645A (en) |
-
1987
- 1987-06-08 JP JP62142759A patent/JPS63309645A/en active Pending
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