JP2002061057A - Highly heat-conductive heat-resistant felt material having excellent abrasion resistance of surface - Google Patents
Highly heat-conductive heat-resistant felt material having excellent abrasion resistance of surfaceInfo
- Publication number
- JP2002061057A JP2002061057A JP2000248704A JP2000248704A JP2002061057A JP 2002061057 A JP2002061057 A JP 2002061057A JP 2000248704 A JP2000248704 A JP 2000248704A JP 2000248704 A JP2000248704 A JP 2000248704A JP 2002061057 A JP2002061057 A JP 2002061057A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- felt
- fiber
- resistant
- thermal conductivity
- 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.)
- Withdrawn
Links
- 239000000463 material Substances 0.000 title claims abstract description 39
- 238000005299 abrasion Methods 0.000 title abstract description 18
- 239000000835 fiber Substances 0.000 claims abstract description 65
- 238000000034 method Methods 0.000 claims abstract description 18
- 239000012210 heat-resistant fiber Substances 0.000 abstract description 9
- 238000004080 punching Methods 0.000 description 24
- 229920000642 polymer Polymers 0.000 description 13
- 239000000047 product Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 229920003235 aromatic polyamide Polymers 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 5
- -1 ferrous metals Chemical class 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 4
- 229920002748 Basalt fiber Polymers 0.000 description 3
- 229920000106 Liquid crystal polymer Polymers 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920000137 polyphosphoric acid Polymers 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229920006231 aramid fiber Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 229940098779 methanesulfonic acid Drugs 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 239000004976 Lyotropic liquid crystal Substances 0.000 description 1
- 229920000784 Nomex Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000004763 nomex Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920002577 polybenzoxazole Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- QXWYLVQTEJWMKW-UHFFFAOYSA-N thieno[3,4-c]pyridine Chemical compound C1=NC=CC2=CSC=C21 QXWYLVQTEJWMKW-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Landscapes
- Nonwoven Fabrics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、鉄鋼、窯業、非鉄
金属分野などの製造工程において、高温製品のキズ防止
を目的とした耐熱クッション材料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat-resistant cushioning material for the purpose of preventing scratches on high-temperature products in the manufacturing process of steel, ceramics, non-ferrous metals and the like.
【0002】[0002]
【従来の技術】鉄鋼、窯業、非鉄金属分野などの製造工
程においては、高温製品にキズを入れることなく製品を
支持する必要があり、主として耐熱性有機繊維からなる
耐熱クッション材料が使用されている。ここで、耐熱性
繊維の素材としてはパラアラミド繊維、メタアラミド繊
維、耐炎化繊維などが一般的に用いられており、耐熱ク
ッション材料としては、該耐熱繊維を単独であるいは複
合して用いられる。それらの例として芳香族ポリアミド
繊維とセラミックファイバーを混綿してニードルパンチ
ングした高耐熱性繊維製緩衝材(例えば特開平7−34
367号公報)、金属繊維や無機繊維を混綿してニード
ルパンチングした高温製品用耐熱フェルト(例えば特開
平08−296160号公報)、玄武岩繊維を主材とし
た耐屈曲性と耐摩耗性を有する無機繊維、金属繊維、耐
熱有機繊維を混入してなる耐熱ニードルフェルト(例え
ば特開平11−200211号公報)等が挙げられる。
しかしながら、金属繊維や無機繊維、玄武岩繊維などか
らなる耐熱クッション材料は、耐熱性有機繊維からなる
耐熱クッション材料と比較して、もろくて硬いため、耐
摩耗性が悪く、また、高温製品にキズを入れてしまうと
いう問題があった。2. Description of the Related Art In a manufacturing process in the fields of steel, ceramics, non-ferrous metals, etc., it is necessary to support a high-temperature product without damaging the product, and a heat-resistant cushion material mainly made of heat-resistant organic fibers is used. . Here, para-aramid fiber, meta-aramid fiber, flame-resistant fiber and the like are generally used as the material of the heat-resistant fiber, and the heat-resistant cushion material is used alone or in combination with the heat-resistant fiber. As an example thereof, a cushioning material made of a high heat-resistant fiber obtained by blending an aromatic polyamide fiber and a ceramic fiber and performing needle punching (for example, JP-A-7-34)
No. 367), a heat-resistant felt for high-temperature products which is needle-punched by blending metal fibers and inorganic fibers (for example, Japanese Patent Application Laid-Open No. 08-296160), and an inorganic material having a basalt fiber as a main material and having bending resistance and wear resistance. Heat-resistant needle felt obtained by mixing fibers, metal fibers, and heat-resistant organic fibers (for example, Japanese Patent Application Laid-Open No. 11-200211).
However, heat-resistant cushion materials made of metal fibers, inorganic fibers, basalt fibers, etc. are fragile and harder than heat-resistant cushion materials made of heat-resistant organic fibers, so they have poor abrasion resistance and also damage high-temperature products. There was a problem of putting it.
【0003】そこで、パラアラミド繊維単体、あるいは
アクリル繊維を熱処理して炭化させた耐炎化繊維( 例
えば商標名「 パイロメックス 」など )等に代表され
る耐熱性繊維との混合物からなる耐熱性クッション材料
はすでに実用化されており、一定の成果を上げている。
しかし、鉄鋼、窯業、非鉄金属分野などの製造工程にお
いては、加工成形直後の高温製品の温度は350℃以上
で使われるケースが多く、上記の耐熱性クッション材料
では寿命が著しく短く、頻繁に交換しなければならない
という問題があった。Therefore, a heat-resistant cushioning material composed of a mixture of heat-resistant fibers typified by para-aramid fibers alone or oxidized fibers made by heat-treating acrylic fibers (for example, trade name "Pyromex") is used. It has already been put into practical use and has achieved certain results.
However, in the manufacturing processes of steel, ceramics, non-ferrous metals, etc., the temperature of high-temperature products immediately after forming is often used at 350 ° C or higher. There was a problem that had to be done.
【0004】また、上記用途における耐熱性クッション
材料は冷却工程で用いられる場合が多く、断熱材といい
ながら高い熱伝導性が望まれており、熱伝導率の低い有
機素材断熱材では十分な冷却効果が得られない問題があ
った。この問題を解決する方法として高熱伝導性耐熱フ
ェルト材料(例えば特願平11-259229号)がすでに出願
されており、高熱伝導性耐熱繊維からなるニードルパン
チフェルトにおいてフェルトの厚み方向よりフェルトの
表面に平行な方向(面内方向)に熱伝導性が極めて高い
という特徴を幾何学的に活用して高熱伝導を実現させて
いる。しかしながら、上記のような幾何学的活用なし
で、フェルトの厚み方向の熱伝導率0.7W/m・K以
上を実現することは今までできなかった。また、ニード
ルパンチング数を増やしていくとニードルパンチング時
に繊維を切断しやすくなり、切断された繊維がフェルト
表面の摩耗性に悪影響してしまう問題点があったため、
これまで、主として高熱伝導性耐熱性有機繊維で構成さ
れた耐熱フェルト材料で、フェルト表面の摩耗性を損な
わず、かつ、フェルトの厚み方向の熱伝導率0.7W/
m・K以上を実現することはできなかった。[0004] In addition, the heat-resistant cushioning material used in the above applications is often used in a cooling step, and a high thermal conductivity is desired even though it is a heat insulating material. There was a problem that the effect could not be obtained. As a method for solving this problem, a high heat conductive heat resistant felt material (for example, Japanese Patent Application No. 11-259229) has already been filed, and in the case of a needle punch felt made of a high heat conductive heat resistant fiber, the surface of the felt is felt from the thickness direction of the felt. High heat conduction is realized by geometrically utilizing the feature that heat conductivity is extremely high in a parallel direction (in-plane direction). However, it has not been possible to achieve a thermal conductivity of 0.7 W / m · K or more in the thickness direction of the felt without the above-described geometrical utilization. Also, increasing the number of needle punching makes it easier to cut the fiber during needle punching, and the cut fiber has a problem of adversely affecting the abrasion of the felt surface.
Heretofore, a heat-resistant felt material mainly composed of a heat-conductive organic fiber having high heat conductivity, without impairing the abrasion of the felt surface, and having a thermal conductivity of 0.7 W / in the thickness direction of the felt.
mK or more could not be realized.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記の欠点
を解決するものであり、その目的は、優れた耐熱性と熱
伝導性を有する繊維からなる、表面耐摩耗性良好な高熱
伝導性耐熱フェルト材料を提供せんとするものである。The object of the present invention is to solve the above-mentioned drawbacks, and an object of the present invention is to provide a high thermal conductivity made of a fiber having excellent heat resistance and thermal conductivity and having good surface wear resistance. It is intended to provide a heat-resistant felt material.
【0006】[0006]
【課題を解決するための手段】本発明者等は、ポリベン
ザゾ−ル繊維や高強度ポリエチレン繊維のように繊維軸
方向に金属並の高い熱伝導率を有する有機繊維を用いた
フェルト材料の場合、熱伝導性を支配するのはフェルト
内の繊維の配向であること、そして、ニードルパンチ製
造条件のうち針深度を最適値に設定することで、パンチ
ングした側と反対側のフェルト面の表面耐摩耗性が大幅
に改善することを見い出し、発明を完成するに至った。Means for Solving the Problems The present inventors have found that in the case of a felt material using an organic fiber having a high thermal conductivity comparable to that of a metal in the fiber axis direction, such as a polybenzazol fiber or a high-strength polyethylene fiber, The thermal conductivity is governed by the orientation of the fibers in the felt, and by setting the needle depth to the optimum value in the needle punch manufacturing conditions, the surface wear resistance of the felt surface opposite to the punched side The inventors have found that the properties have been greatly improved, and have completed the invention.
【0007】即ち、本発明は、主として耐熱性有機繊維
で構成された、見かけ密度が0.2g/cm3以上であ
るフェルト材料で、JIS L 1913テーバ形法により測定し
たフェルトの表面の摩耗強さが4級以上で、かつ、厚み
方向の熱伝導率が0.7W/m・K以上であることを特
徴とする、表面耐摩耗性良好な高熱伝導性耐熱フェルト
材料であり、具体的には耐熱性有機繊維が、ポリベンザ
ゾール繊維であることを特徴とする上記記載の高熱伝導
性耐熱フェルト材料である。以下、本発明を詳述する。That is, the present invention relates to a felt material mainly composed of heat-resistant organic fibers and having an apparent density of 0.2 g / cm 3 or more. Is a high heat conductive heat-resistant felt material having good surface wear resistance, characterized in that the material has a class 4 or higher and a thermal conductivity in the thickness direction of 0.7 W / m · K or more. Is a high heat conductive heat resistant felt material as described above, wherein the heat resistant organic fiber is a polybenzazole fiber. Hereinafter, the present invention will be described in detail.
【0008】ポリベンザゾール繊維とは、ポリベンザゾ
ールポリマーよりなる繊維をいい、ポリベンザゾール
(以下、PBZともいう)とは、ポリベンゾオキサゾー
ル(以下、PBOともいう)ホモポリマー、ポリベンゾ
チアゾール(以下、PBTともいう)ホモポリマーおよ
びPBOとPBTのランダム、シーケンシャルあるいは
ブロック共重合ポリマー等をいう。ここでPBO、PB
Tおよびそれらのランダム、シーケンシャルあるいはブ
ロック共重合ポリマーは、例えばWolfe等の「Liquid Cr
ystalline Polymer Compositions, Process and Produc
ts」米国特許第4703103号(1987年10月2
7日)、「Liquid Crystalline Polymer Compositions,
Process and Products」米国特許第4533692号
(1985年8月6日)、「Liquid Crystalline Poly
(2,6-Benzothiazole) Compositions,Process and Produ
cts」米国特許第4533724号(1985年8月6
日)、「Liquid Crystalline Polymer Compositions, P
rocess and Products」米国特許第4533693号
(1985年8月6日)、Eversの「Thermooxidatively
Stable Articulated p-Benzobisoxazole and -Benzobis
thiazole Polymers」米国特許第4539567号(1
982年11月16日)、Tsai等の「Method formaking
Heterocyclic Block Copolymer」米国特許第4578
432号(1986年3月25日)等に記載されてい
る。[0008] The polybenzazole fiber refers to a fiber made of a polybenzazole polymer, and the polybenzazole (hereinafter, also referred to as PBZ) is a polybenzoxazole (hereinafter, also referred to as PBO) homopolymer, a polybenzothiazole (hereinafter, referred to as PBO). (Hereinafter also referred to as PBT) homopolymer and random, sequential or block copolymer of PBO and PBT. Where PBO, PB
T and their random, sequential or block copolymers are disclosed, for example, in Wolfe et al.
ystalline Polymer Compositions, Process and Produc
ts "U.S. Pat. No. 4,703,103 (October 2, 1987)
7) "Liquid Crystalline Polymer Compositions,
Process and Products, US Patent No. 4,533,692 (August 6, 1985), "Liquid Crystalline Poly"
(2,6-Benzothiazole) Compositions, Process and Produ
cts "U.S. Pat. No. 4,533,724 (August 6, 1985)
Sun), "Liquid Crystalline Polymer Compositions, P
"Rocess and Products" U.S. Pat. No. 4,533,693 (August 6, 1985); Evers, "Thermooxidatively
Stable Articulated p-Benzobisoxazole and -Benzobis
thiazole Polymers "U.S. Pat. No. 4,539,567 (1.
November 16, 982), “Method formaking” by Tsai et al.
Heterocyclic Block Copolymer '' U.S. Pat.
432 (March 25, 1986) and the like.
【0009】PBZポリマーに含まれる構造単位として
は、好ましくはライオトロピック液晶ポリマーから選択
される。当該ポリマーは構造式(a)〜(h)に記載さ
れているモノマー単位から選択され、さらに好ましく
は、本質的に構造式(a)〜(d)から選択されたモノ
マー単位からなる。The structural unit contained in the PBZ polymer is preferably selected from a lyotropic liquid crystal polymer. The polymer is selected from the monomer units described in Structural Formulas (a) to (h), and more preferably consists essentially of the monomer units selected from Structural Formulas (a) to (d).
【0010】[0010]
【化1】 Embedded image
【0011】[0011]
【化2】 Embedded image
【0012】ポリベンザゾール繊維は、PBZポリマー
を含有するドープより製造されるが、当該ドープを調製
するための好適な溶媒としては、クレゾールやそのポリ
マーを溶解しうる非酸化性の酸が挙げられる。好適な非
酸化性の酸の例としては、ポリリン酸、メタンスルホン
酸および高濃度の硫酸あるいはそれらの混合物が挙げら
れる。中でもポリリン酸及びメタンスルホン酸、特にポ
リリン酸が好適である。The polybenzazole fiber is produced from a dope containing a PBZ polymer. Suitable solvents for preparing the dope include cresol and a non-oxidizing acid capable of dissolving the polymer. . Examples of suitable non-oxidizing acids include polyphosphoric acid, methanesulfonic acid and concentrated sulfuric acid or mixtures thereof. Among them, polyphosphoric acid and methanesulfonic acid, particularly polyphosphoric acid, are preferred.
【0013】ドープ中のポリマー濃度は好ましくは少な
くとも約7重量%であり、より好ましくは少なくとも1
0重量%、特に好ましくは少なくとも14重量%であ
る。最大濃度は、例えばポリマーの溶解性やドープ粘度
といった実際上の取り扱い性により限定される。それら
の限界要因のために、ポリマー濃度は通常では20重量
%を越えることはない。[0013] The polymer concentration in the dope is preferably at least about 7% by weight, more preferably at least 1% by weight.
It is 0% by weight, particularly preferably at least 14% by weight. The maximum concentration is limited by practical handling properties such as, for example, polymer solubility and dope viscosity. Because of these limiting factors, the polymer concentration usually does not exceed 20% by weight.
【0014】好適なポリマーやコポリマーあるいはドー
プは公知の手法により合成される。例えばWolfe等の米
国特許第4533693号(1985年8月6日)、Sy
bert等の米国特許第4772678号(1988年9月
20日)、Harrisの米国特許第4847350号(19
89年7月11日)に記載される方法で合成される。P
BZポリマーは、Gregory等の米国特許第508959
1号(1992年2月8日)によると、脱水性の酸溶媒
中での比較的高温、高剪断条件下において高反応速度で
の高分子量化が可能である。このようにして調製される
ドープから公知の方法( 例えば米国特許第5,38
5,702号(1995年1月31日)に記載の方法
)を用いてポリベンザゾール繊維が製造される。得ら
れたポリベンザゾール繊維は、さらに通常の捲縮工程お
よび切断工程が施され、ポリベンザゾール繊維の短繊維
に加工される。[0014] Suitable polymers, copolymers or dopes are synthesized by known techniques. See, for example, Wolfe et al., US Pat. No. 4,533,693 (August 6, 1985);
U.S. Pat. No. 4,772,678 to S. bert et al. (September 20, 1988); U.S. Pat.
(July 11, 1989). P
BZ polymers are described in US Pat. No. 5,085,959 to Gregory et al.
According to No. 1 (February 8, 1992), it is possible to increase the molecular weight at a high reaction rate under a relatively high temperature and high shear condition in a dehydrating acid solvent. From the dope thus prepared, a known method (for example, US Pat.
5,702 (January 31, 1995)) to produce polybenzazole fibers. The obtained polybenzazole fiber is further subjected to a normal crimping step and a cutting step, and is processed into a short fiber of polybenzazole fiber.
【0015】ポリベンザゾール繊維を含むフェルトの製
造方法としては、公知の不織布の製造法が適用可能であ
るが、一般的には、短繊維からウェブを形成しニードル
パンチを行うことにより製造されるニードルパンチ法が
採用される。As a method for producing a felt containing polybenzazole fibers, a known method for producing a nonwoven fabric can be applied. Generally, the felt is produced by forming a web from short fibers and performing needle punching. The needle punch method is adopted.
【0016】該フェルト材料は異種の繊維を混合するこ
とが可能で、熱伝導性の要求が高くなるほど、また、耐
熱性の要求が高くなるほどポリベンザゾール繊維の混合
率を上げることが有効である。ポリベンザゾール繊維の
重量分率は、好ましくは50%以上である。50%未満
ではポリベンザゾール繊維の優れた高熱伝導性、耐熱性
が十分に発揮されない恐れがある。混合する繊維として
は、具体的にはパラアラミド繊維(商標名「 ケブラー
」など)、メタアラミド繊維(商標名「 ノーメックス
」など)、ポリイミド繊維(商標名「 P84 」な
ど)、耐炎化繊維(商標名「 パイロメックス 」な
ど)、柔らかさを兼ね備えた耐熱性繊維が好ましいが、
炭素繊維、ガラス繊維、ステンレス繊維、玄武岩繊維な
どの耐熱性繊維も混合が可能である。混合方法として
は、均一に混合したものをフェルトにするか、あるいは
ポリベンザゾール繊維と混合する繊維を別々にフェルト
とした後これらを2層以上に積層するか、フェルトとし
て成型可能であればいかなる方法でも良い。The felt material can mix different types of fibers, and it is effective to increase the mixing ratio of polybenzazole fibers as the requirement for thermal conductivity increases and as the requirement for heat resistance increases. . The weight fraction of the polybenzazole fiber is preferably at least 50%. If it is less than 50%, the excellent high thermal conductivity and heat resistance of the polybenzazole fiber may not be sufficiently exhibited. Specific examples of the fiber to be mixed include para-aramid fiber (trade name “Kevlar”, etc.), meta-aramid fiber (trade name “Nomex”, etc.), polyimide fiber (trade name “P84”, etc.), and oxidized fiber (trade name “ Pyromex "), and heat-resistant fibers having softness are preferred,
Heat-resistant fibers such as carbon fiber, glass fiber, stainless steel fiber, and basalt fiber can also be mixed. As a mixing method, a fiber that is uniformly mixed is made into a felt, or the fibers to be mixed with the polybenzazole fiber are separately made into felts, and then these are laminated in two or more layers, or any shape can be formed as a felt. A method is also acceptable.
【0017】本発明に係るフェルト材料の第一の特徴
は、該フェルト材料に高熱伝導性耐熱性有機繊維が組成
として含まれている事である。高熱伝導性耐熱性有機繊
維とは、繊維軸方向の熱伝導率が10W/m・K以上で
かつ、昇温速度20℃/分で熱重量分析を行ったとき残
存重量が90%未満になる温度が500℃以上の有機繊
維をいい、ポリベンザゾール繊維の他に、例えば、poly
[2,6-diimidazo[4,5-b:4'5'-e]pyridinylene-1,4(2,5-d
ihydroxy)phenylene]などの剛直な分子構造を持つポリ
マーからなる繊維などが挙げられる。高熱伝導性耐熱性
有機繊維を使用しなければ、フェルト材料の十分な耐熱
性が得られず、かつ、フェルト材料内の繊維配向を制御
しても見かけ密度が低いことによるフェルト自体が有す
る低熱伝導性を大幅に改善できない。A first feature of the felt material according to the present invention is that the felt material contains a high heat conductive organic fiber as a composition. High heat conductivity heat-resistant organic fibers are those having a thermal conductivity of 10 W / m · K or more in the fiber axis direction and a residual weight of less than 90% when subjected to thermogravimetric analysis at a heating rate of 20 ° C./min. Organic fiber whose temperature is 500 ° C or higher. In addition to polybenzazole fiber, for example, poly
[2,6-diimidazo [4,5-b: 4'5'-e] pyridinylene-1,4 (2,5-d
Fibers composed of a polymer having a rigid molecular structure such as [ihydroxy) phenylene]. High heat conductivity Unless heat-resistant organic fibers are used, sufficient heat resistance of the felt material cannot be obtained, and even if the fiber orientation in the felt material is controlled, the apparent density is low. Cannot greatly improve the quality.
【0018】本発明に係るフェルト材料の第二の特徴
は、見かけ密度が0.2〜0.5g/cm3であること
である。これは当該見かけ密度が0.2g/cm3で未
満であると、空気層が多くなり熱伝導性が低下するから
である。そしてクッション性を考慮すると0.5g/c
m3以下が望ましい。好ましくは0.3〜0.4g/c
m3である。The second feature of the felt material according to the present invention is that the apparent density is 0.2 to 0.5 g / cm 3 . This is because if the apparent density is less than 0.2 g / cm 3 , the air layer increases and the thermal conductivity decreases. And 0.5g / c in consideration of cushioning
m 3 or less is desirable. Preferably 0.3 to 0.4 g / c
m is 3.
【0019】短繊維からウェブを形成しニードルパンチ
を行うことにより製造されるフェルトは、ニードルパン
チング数を増やすことで、熱伝導性の高いポリベンザゾ
ール繊維をフェルト厚み方向に配向させることができ
る。図1に、ポリベンザゾール繊維からなるニードルパ
ンチフェルトにおける、フェルトの厚み方向の熱伝導率
とニードルパンチング数の相関関係を示すが、ニードル
パンチング数を増やすことで、本発明に係るフェルト材
料の第三の特徴であるフェルトの厚み方向の熱伝導率が
0.7W/m・K以上とし得る。これにより、一般的に
断熱材とよばれている熱伝導率が0.15W/m・K以
下の素材と比較して、熱伝導性に優れ、搬送時に高温製
品から受け取る熱を耐熱性フェルト材料外に放出しやす
くなり、これにより耐熱性フェルト材料は高寿命とする
ことが可能となる。A felt produced by forming a web from short fibers and performing needle punching can increase the number of needle punches so that polybenzazole fibers having high thermal conductivity can be oriented in the thickness direction of the felt. FIG. 1 shows the correlation between the thermal conductivity in the thickness direction of the felt and the number of needle punching in a needle punch felt made of polybenzazole fiber. By increasing the number of needle punching, the number of needle punching felts according to the present invention can be improved. The thermal conductivity in the thickness direction of the felt, which is the third feature, can be 0.7 W / m · K or more. As a result, compared to a material having a thermal conductivity of 0.15 W / m · K or less, which is generally called a heat insulating material, the material has excellent heat conductivity and receives heat received from a high-temperature product during transportation. It is easy to release to the outside, which allows the heat-resistant felt material to have a long life.
【0020】ここでいう熱伝導率とは、 JIS−A−
1412、ASTM−C−177に準拠した定常GHP
法( GuardedHotPlate法 )により、3
00℃の高温条件下において温度差をつけた2枚の熱板
で耐熱フェルトをはさんで測定した時の熱伝導率の値を
いう。The thermal conductivity referred to here is JIS-A-
1412, steady GHP based on ASTM-C-177
Method (GuardedHotPlate method)
It refers to the value of the thermal conductivity when measured by sandwiching a heat-resistant felt between two hot plates having a temperature difference under a high temperature condition of 00 ° C.
【0021】ニードルパンチ法における製造条件のう
ち、針深度のみ数水準変化させてニードルパンチングし
て得られた、ポリベンザゾール繊維からなる数水準のフ
ェルトの常温表面耐摩耗性を評価したところ、ニードル
パンチングした面の常温表面耐摩耗性は針深度に依存せ
ず良くなかったが、ある針深度でニードルパンチングし
たとき、ニードルパンチングした面と反対側のフェルト
面の常温表面耐摩耗性が非常に良好であった。これよ
り、ニードルパンチ製造条件のうち針深度を最適値に設
定し、ニードルパンチングした面と反対側のフェルト面
が最終仕上がりフェルトの表面になるようフェルト化設
計することで、本発明に係るフェルト材料の第四の特徴
である、JIS L 1913テーバ形法により測定したフェルト
の表面の摩耗強さが4級以上とし得る。これにより、フ
ェルト表面の常温耐摩耗性が向上し、フェルト表面から
の繊維の素抜けが抑制されるため、耐熱性フェルト材料
はさらに高寿命とすることが可能となる。Of the manufacturing conditions in the needle punching method, the room temperature surface abrasion resistance of several levels of felt made of polybenzazole fibers obtained by needle punching with only a few changes in the needle depth was evaluated. Room temperature surface wear resistance of the punched surface was not good regardless of the needle depth, but when needle punching was performed at a certain needle depth, the room temperature surface wear resistance of the felt surface opposite to the needle punched surface was very good Met. Thus, the felt material according to the present invention, by setting the needle depth to the optimum value among the needle punch manufacturing conditions and designing the felt so that the felt surface opposite to the needle punched surface becomes the surface of the final finished felt. The fourth feature of the present invention is that the surface of the felt measured by the JIS L 1913 Taber method has a wear strength of class 4 or higher. As a result, the room temperature wear resistance of the felt surface is improved, and the removal of fibers from the felt surface is suppressed, so that the heat-resistant felt material can have a longer life.
【0022】ここでいう常温表面耐摩耗性とは、JIS
L 1913テーバ形法により測定したフェルトの表面
の摩耗強さをいう。The normal temperature surface abrasion resistance referred to herein is JIS.
L 1913 Refers to the abrasion strength of the felt surface measured by the Taber method.
【0023】本発明の高熱伝導性耐熱フェルト材料は、
アルミニウム、鉄、銅などの金属成形分野やセラミック
スの成形分野などにおける高温物を搬送する用途に使用
可能であり、その温度範囲、使用用途を問うものではな
いが、特に300℃以上、さらには400℃以上の高温
物を搬送にする場合にその効果を発揮できる。The high heat conductive heat-resistant felt material of the present invention comprises:
It can be used for transporting high-temperature objects in the field of metal forming such as aluminum, iron, copper, etc., and in the field of forming ceramics, and its temperature range and usage are not limited. The effect can be exerted when conveying a high-temperature object of at least ℃.
【0024】[0024]
【実施例】以下、実施例をもって本特許を説明するが、
本発明は実施例に拘束されるものではない。EXAMPLES The present invention will be described below with reference to examples.
The present invention is not limited to the embodiments.
【0025】(実施例1)東洋紡績(株)製、繊度1.
5デニール、カット長44mmのPBO繊維ステープル
をオープナーにより開綿後ローラーカードにより目付4
00g/m2 のウェブを作製し、得られたウェブを順次
積層し、Foster社製ニードル(品番:15×18
×40×3.5PB−A F20 2−18−3B/LI
/CC/CONICAL)を用いて、針深度7mmで、
フェルトの片側面からのみ合計ニードルパンチング数2
000/cm2になるまでニードルパンチング実施、厚
み9.5mm、目付3600g/m2、密度0.38g
/m3のフェルトを得た。パンチングした面と反対側の
面をフェルト表面とした。成形したフェルト材料の熱伝
導性の評価として、JIS−A−1412に準じて、3
00℃の条件下での熱伝導率測定( 試験板面積100
cm2、試験板温度差10℃ )を行ったところ、熱伝導
率は1.07W/m・Kであった。また、成形したフェ
ルト材料の常温表面耐摩耗性の評価として、JIS L
1913テーバ形法により耐摩耗性を評価した結果、フ
ェルトの表面の摩耗強さは4級であった。さらに、図2
に示すような高温耐摩耗試験機を用いて、400℃に加
熱した摩擦子を500g/cm2 の荷重下で試料に接触
させた状態で試料を300rpmで回転させた時の50
時間後の摩耗による重量減少量で耐摩耗性を評価したと
ころ、摩耗量は2.0mg/cm2 であった。(Example 1) Fineness of 1. manufactured by Toyobo Co., Ltd.
5 denier, 44 mm cut length PBO fiber staple is opened with an opener and then weighted with a roller card 4
A web of 00 g / m 2 was prepared, and the obtained webs were sequentially laminated to form a needle manufactured by Foster (product number: 15 × 18).
× 40 × 3.5PB-A F20 2-18-3B / LI
/ CC / CONICAL) at a needle depth of 7 mm,
Needle punching number 2 only from one side of felt
Needle punching until 000 / cm 2 , thickness 9.5 mm, basis weight 3600 g / m 2 , density 0.38 g
/ M 3 of felt. The surface opposite to the punched surface was taken as a felt surface. The thermal conductivity of the formed felt material was evaluated as 3 in accordance with JIS-A-1412.
Thermal conductivity measurement under the condition of 00 ° C (test plate area 100
cm 2 and a test plate temperature difference of 10 ° C.), the thermal conductivity was 1.07 W / m · K. In addition, JIS L
As a result of evaluating the abrasion resistance by the 1913 Taber method, the abrasion strength of the felt surface was quaternary. Further, FIG.
Using a high-temperature wear test machine such as that shown in, 50 when the sample is rotated at 300rpm a heated friction element to 400 ° C. in a state of being contact with the sample under a load of 500 g / cm 2
When the abrasion resistance was evaluated based on the weight loss due to abrasion after time, the abrasion amount was 2.0 mg / cm 2 .
【0026】(実施例2)針深度を9mmに変更して、
他のニードルパンチング条件は実施例1と同様にしてニ
ードルパンチングを実施、厚み9.0mm、目付360
0g/m2、密度0.40g/m3のフェルトを得た。パ
ンチングした面と反対側の面をフェルト表面とした。実
施例1と同様に熱伝導率測定と表面耐摩耗性、高温耐摩
耗性試験を行ったところ、熱伝導率は1.02W/m・
K、フェルトの表面の摩耗強さは4級、高温耐摩耗試験
による摩耗量は2.3mg/cm2 であった。(Embodiment 2) Changing the needle depth to 9 mm,
Other needle punching conditions were the same as in Example 1, needle punching was performed, the thickness was 9.0 mm, and the basis weight was 360.
A felt having a density of 0 g / m 2 and a density of 0.40 g / m 3 was obtained. The surface opposite to the punched surface was taken as a felt surface. When the thermal conductivity was measured and the surface wear resistance and the high-temperature wear resistance test were performed in the same manner as in Example 1, the thermal conductivity was 1.02 W / m ·.
The wear strength of the surface of K and felt was grade 4, and the amount of wear in a high-temperature wear resistance test was 2.3 mg / cm 2 .
【0027】(比較例1)実施例1と全く同じニードル
パンチング条件にてニードルパンチングを実施、厚み
9.5mm、目付3600g/m2、密度0.38g/
m3のフェルトを得た。パンチングした面をフェルト表
面とした。実施例1と同様に熱伝導率測定と表面耐摩耗
性、高温耐摩耗性試験を行ったところ、熱伝導率は1.
07W/m・K、フェルトの表面の摩耗強さは3級、高
温耐摩耗試験による摩耗量は6.0mg/cm2 であっ
た。(Comparative Example 1) Needle punching was performed under exactly the same needle punching conditions as in Example 1, thickness 9.5 mm, basis weight 3600 g / m 2 , density 0.38 g /
m 3 of felt was obtained. The punched surface was used as a felt surface. The thermal conductivity was measured and the surface wear resistance and the high-temperature wear resistance test were performed in the same manner as in Example 1. As a result, the thermal conductivity was 1.
07 W / m · K, the wear strength of the felt surface was class 3, and the wear amount by a high-temperature wear resistance test was 6.0 mg / cm 2 .
【0028】(比較例2)実施例2と全く同じニードル
パンチング条件にてニードルパンチングを実施、厚み
9.0mm、目付3600g/m2、密度0.4g/m3
のフェルトを得た。パンチングした面をフェルト表面と
した。実施例1と同様に熱伝導率測定と表面耐摩耗性、
高温耐摩耗性試験を行ったところ、熱伝導率は1.02
W/m・K、フェルトの表面の摩耗強さは3級、高温耐
摩耗試験による摩耗量は5.0mg/cm2 であった。(Comparative Example 2) Needle punching was carried out under exactly the same needle punching conditions as in Example 2, thickness 9.0 mm, basis weight 3600 g / m 2 , density 0.4 g / m 3
Got the felt. The punched surface was used as a felt surface. Thermal conductivity measurement and surface wear resistance as in Example 1,
A high-temperature wear resistance test showed that the thermal conductivity was 1.02.
W / m · K, the wear strength of the felt surface was grade 3, and the wear amount by a high-temperature wear resistance test was 5.0 mg / cm 2 .
【0029】(比較例3)針深度を5mmに変更して、
他のニードルパンチング条件は実施例1と同様にしてニ
ードルパンチングを実施、厚み10.5mm、目付36
00g/m2、密度0.34g/m3のフェルトを得た。
パンチングした面と反対側の面をフェルト表面とした。
実施例1と同様に熱伝導率測定と表面耐摩耗性、高温耐
摩耗性試験を行ったところ、熱伝導率は0.95W/m
・K、フェルトの表面の摩耗強さは3級、高温耐摩耗試
験による摩耗量は9.5mg/cm2 であった。(Comparative Example 3) The needle depth was changed to 5 mm,
Other needle punching conditions were the same as in Example 1, needle punching was performed, thickness was 10.5 mm, and basis weight was 36.
A felt having a density of 00 g / m 2 and a density of 0.34 g / m 3 was obtained.
The surface opposite to the punched surface was taken as a felt surface.
When the thermal conductivity measurement, the surface wear resistance and the high-temperature wear resistance test were performed in the same manner as in Example 1, the thermal conductivity was 0.95 W / m.
-The wear strength of the surface of K and felt was grade 3, and the amount of wear in a high temperature wear resistance test was 9.5 mg / cm 2 .
【0030】(比較例4)比較例3と同様にニードルパ
ンチングを実施、厚み10.5mm、目付3600g/
m2、密度0.34g/m3のフェルトを得た。パンチン
グした面をフェルト表面とした。実施例1と同様に熱伝
導率測定と表面耐摩耗性、高温耐摩耗性試験を行ったと
ころ、熱伝導率は0.95W/m・K、フェルトの表面
の摩耗強さは3級、高温耐摩耗試験による摩耗量は1
0.5mg/cm2 であった。(Comparative Example 4) Needle punching was carried out in the same manner as in Comparative Example 3, with a thickness of 10.5 mm and a basis weight of 3600 g /
A felt having m 2 and a density of 0.34 g / m 3 was obtained. The punched surface was used as a felt surface. When the thermal conductivity was measured and the surface wear resistance and the high-temperature wear resistance test were performed in the same manner as in Example 1, the thermal conductivity was 0.95 W / m · K, the wear strength of the felt surface was grade 3, and the temperature was high. The wear amount by the wear resistance test is 1
It was 0.5 mg / cm 2 .
【0031】(比較例5)パラアラミドの44mmカッ
ト長のステープルを用いてニードルパンチングによって
厚み11.0mm、目付3600g/m2、密度0.3
3g/m3のフェルトを得た。実施例1と同様に熱伝導
率測定と表面耐摩耗性、高温耐摩耗性試験を行ったとこ
ろ、熱伝導率は0.24W/m・K、フェルトの表面の
摩耗強さは4級、高温耐摩耗試験による摩耗量は63.
4mg/cm2 であった。(Comparative Example 5) A thickness of 11.0 mm, a basis weight of 3600 g / m 2 , and a density of 0.3 were prepared by needle punching using a staple of 44 mm cut length of para-aramid.
3 g / m 3 of felt was obtained. When the thermal conductivity was measured and the surface wear resistance and the high-temperature wear resistance test were performed in the same manner as in Example 1, the thermal conductivity was 0.24 W / m · K, the wear strength of the felt surface was grade 4, and the temperature was high. The amount of abrasion in the abrasion resistance test was 63.
It was 4 mg / cm 2 .
【0032】(比較例6)パラアラミドと耐炎化繊維の
ステープルを3:7の割合で混合し、ニードルパンチン
グによって厚み11.0mm、目付3900g/m2、
密度0.35g/m3のフェルトを得た。実施例1と同
様に熱伝導率測定と表面耐摩耗性、高温耐摩耗性試験を
行ったところ、熱伝導率は0.27W/m・K、フェル
トの表面の摩耗強さは4級、高温耐摩耗試験による摩耗
量は119.3mg/cm2 であった。Comparative Example 6 A staple of para-aramid and oxidized fiber was mixed at a ratio of 3: 7, and the resulting mixture was needle-punched to have a thickness of 11.0 mm and a basis weight of 3900 g / m 2 .
A felt having a density of 0.35 g / m 3 was obtained. When the thermal conductivity was measured and the surface wear resistance and the high-temperature wear resistance test were performed in the same manner as in Example 1, the thermal conductivity was 0.27 W / m · K, the wear strength of the felt surface was grade 4, and the temperature was high. The abrasion loss in the abrasion resistance test was 119.3 mg / cm 2 .
【0033】以上の実験結果を表1にまとめる。比較例
と比べ、実施例のフェルトは耐熱性、熱伝導性に優れ、
フェルト表面の耐摩耗性、特に高温での耐摩耗性に圧倒
的に優れていることが明らかである。Table 1 summarizes the above experimental results. Compared with the comparative example, the felts of the examples have excellent heat resistance and thermal conductivity,
It is clear that the wear resistance of the felt surface, especially at high temperatures, is by far the best.
【0034】[0034]
【表1】 [Table 1]
【0035】[0035]
【発明の効果】本発明によると、優れた熱伝導性を有す
る耐熱性繊維からなる、表面耐摩耗性が良好な高熱伝導
性耐熱フェルト材料を提供することを可能とした。According to the present invention, it has become possible to provide a high heat conductive heat resistant felt material made of heat resistant fibers having excellent heat conductivity and having good surface wear resistance.
【図1】フェルトの厚み方向の熱伝導率とニードルパン
チング数の相関関係を示すグラフ。FIG. 1 is a graph showing the correlation between the thermal conductivity in the thickness direction of the felt and the number of needle punching.
【図2】耐摩耗性の測定で使用する高温耐摩耗測定器を
示す概要図。FIG. 2 is a schematic diagram showing a high-temperature wear resistance measuring instrument used for measuring wear resistance.
1 高熱伝導性耐熱性フェルト 2 ヒーター 3 摩擦子 4 重り 5 モーター 6 サンプルフォルダー 7 サンプル DESCRIPTION OF SYMBOLS 1 High thermal conductive heat resistant felt 2 Heater 3 Friction element 4 Weight 5 Motor 6 Sample folder 7 Sample
Claims (2)
かけ密度が0.2g/cm3以上であるフェルト材料
で、厚み方向の熱伝導率が0.7W/m・K以上であ
り、かつ、JIS L 1913テーバ形法により測定し
たフェルトの表面の摩耗強さが4級以上であることを特
徴とする表面耐摩耗性良好な高熱伝導性耐熱フェルト材
料。1. A felt material mainly composed of heat-resistant organic fibers having an apparent density of 0.2 g / cm 3 or more, a thermal conductivity in a thickness direction of 0.7 W / m · K or more, and A high heat conductive heat resistant felt material having good surface wear resistance, characterized in that the surface of the felt has a wear resistance of at least class 4 as measured by JIS L 1913 Taber method.
あることを特徴とする請求項1記載の表面耐摩耗性良好
な高熱伝導性耐熱フェルト材料。2. The high heat conductive heat resistant felt material having good surface wear resistance according to claim 1, wherein the heat resistant organic fiber is a polybenzazole fiber.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000248704A JP2002061057A (en) | 2000-08-18 | 2000-08-18 | Highly heat-conductive heat-resistant felt material having excellent abrasion resistance of surface |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000248704A JP2002061057A (en) | 2000-08-18 | 2000-08-18 | Highly heat-conductive heat-resistant felt material having excellent abrasion resistance of surface |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002061057A true JP2002061057A (en) | 2002-02-28 |
Family
ID=18738562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000248704A Withdrawn JP2002061057A (en) | 2000-08-18 | 2000-08-18 | Highly heat-conductive heat-resistant felt material having excellent abrasion resistance of surface |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002061057A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003039832A1 (en) * | 2001-11-09 | 2003-05-15 | Yamauchi Corporation | Cushioning material for hot pressing and process for producing layered board |
| JP2008202155A (en) * | 2007-02-19 | 2008-09-04 | Toyobo Co Ltd | Spark receiving sheet |
| WO2010007917A1 (en) * | 2008-07-15 | 2010-01-21 | イチカワ株式会社 | Heat resistant cushion material for molding press |
| JP2010236130A (en) * | 2009-03-31 | 2010-10-21 | Toyobo Co Ltd | Comfortable fabric |
| JP4820920B2 (en) * | 2008-07-15 | 2011-11-24 | イチカワ株式会社 | Heat-resistant cushioning material for molding press |
-
2000
- 2000-08-18 JP JP2000248704A patent/JP2002061057A/en not_active Withdrawn
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003039832A1 (en) * | 2001-11-09 | 2003-05-15 | Yamauchi Corporation | Cushioning material for hot pressing and process for producing layered board |
| JP2008202155A (en) * | 2007-02-19 | 2008-09-04 | Toyobo Co Ltd | Spark receiving sheet |
| WO2010007917A1 (en) * | 2008-07-15 | 2010-01-21 | イチカワ株式会社 | Heat resistant cushion material for molding press |
| WO2010007662A1 (en) * | 2008-07-15 | 2010-01-21 | イチカワ株式会社 | Heat-resistant cushion material for forming press |
| JP4820920B2 (en) * | 2008-07-15 | 2011-11-24 | イチカワ株式会社 | Heat-resistant cushioning material for molding press |
| TWI383893B (en) * | 2008-07-15 | 2013-02-01 | Ichikawa Co Ltd | Heat-resistant cushioning member for pressing |
| JP2010236130A (en) * | 2009-03-31 | 2010-10-21 | Toyobo Co Ltd | Comfortable fabric |
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