JPH0249341B2 - FUENOORUJUSHISEIKEIZAIRYO - Google Patents
FUENOORUJUSHISEIKEIZAIRYOInfo
- Publication number
- JPH0249341B2 JPH0249341B2 JP9585683A JP9585683A JPH0249341B2 JP H0249341 B2 JPH0249341 B2 JP H0249341B2 JP 9585683 A JP9585683 A JP 9585683A JP 9585683 A JP9585683 A JP 9585683A JP H0249341 B2 JPH0249341 B2 JP H0249341B2
- Authority
- JP
- Japan
- Prior art keywords
- molding material
- phenolic resin
- xylene
- resins
- 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 - Lifetime
Links
- 239000005011 phenolic resin Substances 0.000 claims description 29
- 239000012778 molding material Substances 0.000 claims description 28
- 229920001568 phenolic resin Polymers 0.000 claims description 26
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 19
- 239000003365 glass fiber Substances 0.000 claims description 13
- 229910052582 BN Inorganic materials 0.000 claims description 12
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 12
- 239000000835 fiber Substances 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 239000008096 xylene Substances 0.000 claims description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000005299 abrasion Methods 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 239000011134 resol-type phenolic resin Substances 0.000 description 4
- 244000144992 flock Species 0.000 description 3
- 239000004312 hexamethylene tetramine Substances 0.000 description 3
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000010680 novolac-type phenolic resin Substances 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- OIAUFEASXQPCFE-UHFFFAOYSA-N formaldehyde;1,3-xylene Chemical compound O=C.CC1=CC=CC(C)=C1 OIAUFEASXQPCFE-UHFFFAOYSA-N 0.000 description 2
- 239000006082 mold release agent Substances 0.000 description 2
- -1 phenol and cresol Chemical class 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 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 1
- 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
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
Description
[発明の技術分野]
本発明は、耐熱性、機械的強度、耐摩耗性およ
び電気特性に優れたフエノール樹脂成形材料に関
する。
[発明の技術的背景とその問題点]
フエノール樹脂は、充填剤、可塑剤、着色剤、
離形剤などを混合・混練した成形材料として幅広
く使用されている。
一般的にフエノール樹脂成形材料は、主充填剤
として木粉を用いるため、耐熱性、機械的強度お
よび耐摩耗性などに欠点があつた。この欠点を改
良するものとしてアスベスト、炭酸カルシウムお
よびタルク等の無機質を充填剤として用いたもの
がある。これは耐熱性は改良されるものの機械的
強度および対摩耗性に難点がある。これを改良し
ようとグラフアイトおよび二硫化モリブデンを充
填剤として用いたものがあるが耐摩耗性について
は改良されるものの機械的強度、電気特性に欠点
がある。これを改良しようとガラス繊維を充填剤
として用いたものは耐熱性、機械的強度は強いが
耐摩耗性(特に相手金属材料の摩耗)に欠点があ
つた。また、天然有機繊維を充填剤として使用し
たものは、機械的強度および耐摩耗性は良いが耐
熱性に欠ける。このような状況で優れた耐熱性、
機械的強度、耐摩耗性および電気特性を有するバ
ランスのとれたフエノール樹脂成形材料が求めら
れていた。
[発明の目的]
本発明の目的は、上記の欠点を解消する耐熱
性、機械的強度、耐摩耗性および電気特性の優れ
たバランスの良いフエノール樹脂成形材料を提供
しようとするものである。
[発明の概要]
本発明は、上記の目的を達成すべく鋭意研究を
重ねた結果、後述する成形材料が上記目的特性を
有することを見い出したものである。
即ち本発明は、
(a) フエノール樹脂、キシレン樹脂及びキシレン
変性フエノール樹脂のなかから選ばれる1種又
は2種以上の樹脂
(b) ガラス繊維
(c) 天然有機繊維
(d) ボロンナイトライド
を主成分とすることを特徴とするフエノール樹脂
成形材料で、成形材料に対してガラス繊維5〜40
重量%、天然有機繊維5〜30重量%、ボロンナイ
トライド1〜30重量%含有し耐熱性、機械的強
度、耐摩耗性および電気特性に優れたバランスの
とれたフエノール樹脂成形材料である。
本発明に用いる(a)フエノール樹脂、キシレン樹
脂及びキシレン変性フエノール樹脂のなかから選
ばれる1種又は2種以上の樹脂としては以下のも
のが挙げられる。フエノール樹脂としては、例え
ばフエノール、クレゾール等のフエノール類、又
は糖密、リグニン、キシレン、ナフタレンもしく
は石油系芳香族炭化水素による変性フエノール類
と、ホルマリン、パラホルムアルデヒド類とを適
宜のモル比に配合し、触媒下で反応させて得られ
た、ノボラツク型フエノール樹脂初期縮合物、レ
ゾール型フエノール樹脂初期縮合物およびノボラ
ツク型フエノール樹脂初期縮合物とレゾール型フ
エノール樹脂初期縮合物との混合物が挙げられ
る。キシレン樹脂もしくはキシレン変性フエノー
ル樹脂としては、キシレンホルムアルデヒド樹脂
又はキシレンホルムアルデヒド樹脂をフエノール
もしくはアルキルフエノールと反応させたキシレ
ン変性フエノール樹脂などが挙げられる。
本発明の用いる(b)ガラス繊維としては、2〜
30μ径の単繊維が収束されたストランドを0.1〜25
mmに切断したもの等が挙げられる。
また、本発明に用いる(c)天然有機繊維として
は、綿フロツク、α−セルロース、亜麻、大麻、
黄麻、綿織布、綿毛粉等が挙げられる。
更に、本発明に用いる(d)ボロンナイトライドと
しては、例えば電気化学工業社製ボロンナイトラ
イドがある。
上述の如く、本発明は(a)フエノール樹脂、キシ
レン樹脂及びキシレン変性フエノール樹脂のなか
から選ばれる1種又は2種以上の樹脂、(b)ガラス
繊維、(c)有機天然繊維、(d)ボロンナイトライドを
主成分とするフエノール樹脂成形材料であるが各
成分の配合割合を次に説明する。
ガラス繊維の配合割合は、成形材料に対して5
〜40重量%配合され、5重量%未満では機械的強
度が弱く、また40重量%を超えると耐摩耗性が悪
く好ましくない。望ましくは15〜25重量%であ
る。天然有機繊維の配合割合は、成形材料に対し
て5〜30重量%で、5重量%未満では、機械的強
度が弱く、30重量%を超えると耐熱性が悪くなり
好ましくない。望ましくは8〜20重量%の範囲内
である。ボロンナイトライド配合割合は、成形材
料に対して1〜30重量%で、1重量%未満では耐
耗性および耐熱性に効果なく、30重量%を超える
と機械的強度が劣り好ましくない。従つて各成分
は上記の範囲内に限定される。
本発明のフエノール樹脂成形材料は、上記の他
に必要に応じ、硬化剤、着色剤、硬化促進剤、難
燃剤、離形剤、滑剤、カツプリング処理剤、可塑
剤等の添加剤を配合することができる。
本発明の成形材料は、通常次のようにして製造
される。所定量の樹脂、ガラス繊維、天然有機繊
維およびボロンナイトライド、必要に応じ硬化剤
その他の添加剤を加えて混合し、均一に分散させ
たのち、混練機で加熱混練し、次いで冷却固化さ
せて粉砕機で適当な大きさに粉砕してフエノール
樹脂成形材料とする。
[発明の効果]
本発明のフエノール樹脂成形材料は、耐熱性が
高く、機械的強度が高く、耐摩耗性および電気特
性に優れており、極めてバランスのよい成形材料
である。
[発明の実施例]
以下、本発明を実施例により具体的に説明する
が、本発明はこれらの実施例によつて限定される
ものではない。以下「%」とは「重量%」を意味
する。
実施例 1
ノボラツク型フエノール樹脂45%にヘキサメチ
レンテトラミン7%、ガラス繊維20%、綿フロツ
ク10%、ボロンナイトライド10%、その他添加剤
8%を常温で混合し、90〜110℃で混練して冷却
した後、粉砕してフエノール樹脂成形材料を得
た。得られた成形材料を圧縮成形および射出成形
で170℃に加熱した金型で成形硬化させて成形品
とした。この成形品について各種の特性を測定し
たので第1表に示した。
実施例 2
ノボラツク型フエノール樹脂40%、キシレン変
性フエノール樹脂5%にヘキサメチレンテトラミ
ン7%、ガラス繊維20%、綿フロツク10%、ボロ
ンナイトライド10%、その他添加剤8%を常温で
混合し、90〜110℃で混練した後、冷却、粉砕し
てフエノール樹脂成形材料を得た。得られた成形
材料を実施例1と同様に成形品をつくりその特性
を測定したので第1表に示した。
実施例 3
レゾール型フエノール樹脂50%、ガラス繊維15
%、綿織布15%、ボロンナイトライド15%、その
他添加剤5%を実施例1と同様の方法により成形
材料を得て、次いで成形品を作りその特性を測定
したので第1表に示した。
比較例 1
ノボラツク型フエノール樹脂50%にヘキサメチ
レンテトラミン8%木粉35%、その他添加剤7%
を実施例1と同様の方法により成形材料を得て、
次いで成形品を作りその特性を測定したので第1
表に示した。
比較例 2
レゾール型フエノール樹脂40%、キシレン変性
フエノール樹脂10%にガラス繊維15%、綿織布15
%、カオリンクレー15%、その他添加剤5%を実
施例と同様の方法により成形材料を得た。次いで
成形品を作りその特性を測定したので第1表に示
した。
[Technical Field of the Invention] The present invention relates to a phenolic resin molding material that has excellent heat resistance, mechanical strength, abrasion resistance, and electrical properties. [Technical background of the invention and its problems] Phenol resin is a filler, a plasticizer, a colorant,
It is widely used as a molding material mixed and kneaded with mold release agents. Generally, phenolic resin molding materials use wood flour as the main filler, so they have drawbacks such as heat resistance, mechanical strength, and abrasion resistance. To improve this drawback, there are methods using inorganic materials such as asbestos, calcium carbonate, and talc as fillers. Although this improves heat resistance, it has drawbacks in mechanical strength and wear resistance. In an attempt to improve this, there are methods using graphite and molybdenum disulfide as fillers, but although the wear resistance is improved, there are drawbacks in mechanical strength and electrical properties. In an attempt to improve this, products using glass fiber as a filler had high heat resistance and mechanical strength, but had drawbacks in abrasion resistance (especially abrasion of the mating metal material). Furthermore, those using natural organic fibers as fillers have good mechanical strength and abrasion resistance, but lack heat resistance. Excellent heat resistance in such situations,
There was a need for a phenolic resin molding material with well-balanced mechanical strength, wear resistance and electrical properties. [Object of the Invention] An object of the present invention is to provide a well-balanced phenolic resin molding material with excellent heat resistance, mechanical strength, abrasion resistance, and electrical properties that eliminates the above-mentioned drawbacks. [Summary of the Invention] In the present invention, as a result of intensive research to achieve the above-mentioned object, it was discovered that a molding material described below has the above-mentioned desired characteristics. That is, the present invention mainly comprises (a) one or more resins selected from phenolic resins, xylene resins, and xylene-modified phenolic resins, (b) glass fibers, (c) natural organic fibers, and (d) boron nitride. A phenolic resin molding material characterized by containing 5 to 40% glass fiber in the molding material.
It is a well-balanced phenolic resin molding material containing 5-30% by weight of natural organic fibers and 1-30% by weight of boron nitride, and has excellent heat resistance, mechanical strength, abrasion resistance, and electrical properties. The one or more resins selected from (a) phenolic resins, xylene resins and xylene-modified phenolic resins used in the present invention include the following. As the phenolic resin, for example, phenols such as phenol and cresol, or phenols modified with molasses, lignin, xylene, naphthalene, or petroleum aromatic hydrocarbons, and formalin or paraformaldehyde are blended in an appropriate molar ratio. , a novolak-type phenolic resin initial condensate, a resol-type phenolic resin initial condensate, and a mixture of a novolak-type phenolic resin initial condensate and a resol-type phenolic resin initial condensate, which are obtained by reaction under a catalyst. Examples of the xylene resin or xylene-modified phenol resin include xylene formaldehyde resin or xylene-modified phenol resin obtained by reacting xylene formaldehyde resin with phenol or alkylphenol. The glass fiber (b) used in the present invention is 2-
0.1~25 strands of single fibers with a diameter of 30μ
Examples include those cut into mm. In addition, (c) natural organic fibers used in the present invention include cotton flock, α-cellulose, flax, hemp,
Examples include jute, cotton woven fabric, and fluff powder. Furthermore, as (d) boron nitride used in the present invention, there is, for example, boron nitride manufactured by Denki Kagaku Kogyo Co., Ltd. As mentioned above, the present invention comprises (a) one or more resins selected from phenolic resins, xylene resins, and xylene-modified phenolic resins, (b) glass fibers, (c) organic natural fibers, (d) This is a phenolic resin molding material whose main component is boron nitride, and the blending ratio of each component will be explained below. The blending ratio of glass fiber is 5% to the molding material.
If the content is less than 5% by weight, the mechanical strength will be weak, and if it exceeds 40% by weight, the abrasion resistance will be poor, which is not preferred. It is preferably 15 to 25% by weight. The blending ratio of natural organic fibers is 5 to 30% by weight based on the molding material. If it is less than 5% by weight, the mechanical strength will be weak, and if it exceeds 30% by weight, the heat resistance will be poor, which is not preferable. It is preferably within the range of 8 to 20% by weight. The blending ratio of boron nitride is 1 to 30% by weight based on the molding material. If it is less than 1% by weight, it has no effect on wear resistance and heat resistance, and if it exceeds 30% by weight, the mechanical strength is poor, which is not preferable. Therefore, each component is limited within the above range. In addition to the above, the phenolic resin molding material of the present invention may contain additives such as a curing agent, a coloring agent, a curing accelerator, a flame retardant, a mold release agent, a lubricant, a coupling agent, a plasticizer, etc., as necessary. Can be done. The molding material of the present invention is usually produced as follows. A predetermined amount of resin, glass fiber, natural organic fiber, and boron nitride, as well as curing agents and other additives as necessary, are added and mixed, uniformly dispersed, heated and kneaded in a kneader, and then cooled and solidified. It is crushed into an appropriate size using a crusher to obtain a phenolic resin molding material. [Effects of the Invention] The phenolic resin molding material of the present invention has high heat resistance, high mechanical strength, excellent wear resistance and electrical properties, and is an extremely well-balanced molding material. [Examples of the Invention] Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these Examples. Hereinafter, "%" means "% by weight". Example 1 45% novolac type phenolic resin, 7% hexamethylenetetramine, 20% glass fiber, 10% cotton flock, 10% boron nitride, and 8% other additives were mixed at room temperature and kneaded at 90 to 110°C. After cooling, the mixture was pulverized to obtain a phenolic resin molding material. The obtained molding material was molded and cured in a mold heated to 170°C by compression molding and injection molding to obtain a molded product. Various properties of this molded article were measured and are shown in Table 1. Example 2 40% novolac type phenolic resin, 5% xylene-modified phenolic resin, 7% hexamethylenetetramine, 20% glass fiber, 10% cotton flock, 10% boron nitride, and 8% other additives were mixed at room temperature, After kneading at 90 to 110°C, the mixture was cooled and pulverized to obtain a phenolic resin molding material. A molded article was made from the obtained molding material in the same manner as in Example 1, and its properties were measured and are shown in Table 1. Example 3 50% resol type phenolic resin, 15% glass fiber
%, 15% cotton woven fabric, 15% boron nitride, and 5% other additives were obtained in the same manner as in Example 1, and then molded products were made and their properties were measured, as shown in Table 1. Ta. Comparative Example 1 50% novolac type phenolic resin, 8% hexamethylenetetramine, 35% wood flour, and 7% other additives.
A molding material was obtained by the same method as in Example 1,
Next, we made a molded product and measured its characteristics, so the first step was to
Shown in the table. Comparative Example 2 40% resol type phenolic resin, 10% xylene modified phenolic resin, 15% glass fiber, 15% cotton woven fabric
%, 15% kaolin clay, and 5% other additives to obtain a molding material in the same manner as in the example. Next, molded products were made and their properties were measured and are shown in Table 1.
【表】
第1表から明らかなように本発明のフエノール
樹脂成形材料は、耐熱性、機械的強度、耐摩耗
性、電気特性の優れていることが認められた。[Table] As is clear from Table 1, the phenolic resin molding material of the present invention was found to be excellent in heat resistance, mechanical strength, abrasion resistance, and electrical properties.
Claims (1)
レン変性フエノール樹脂のなかから選ばれる1
種又は2種以上の樹脂 (b) ガラス繊維 (c) 天然有機繊維 (d) ボロンナイトライド を主成分とすることを特徴とするフエノール樹脂
成形材料。 2 成形材料に対し、ガラス繊維5〜40重量%、
天然有機繊維5〜30重量%、ボロンナイトライド
1〜30重量%含有することを特徴とする特許請求
の範囲第1項記載のフエノール樹脂成形材料。[Scope of Claims] 1 (a) 1 selected from phenolic resins, xylene resins, and xylene-modified phenolic resins;
A phenolic resin molding material characterized in that the main component is a species or two or more kinds of resins (b) glass fibers (c) natural organic fibers (d) boron nitride. 2 Glass fiber 5-40% by weight based on the molding material,
The phenolic resin molding material according to claim 1, characterized in that it contains 5 to 30% by weight of natural organic fibers and 1 to 30% by weight of boron nitride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9585683A JPH0249341B2 (en) | 1983-06-01 | 1983-06-01 | FUENOORUJUSHISEIKEIZAIRYO |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9585683A JPH0249341B2 (en) | 1983-06-01 | 1983-06-01 | FUENOORUJUSHISEIKEIZAIRYO |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59221351A JPS59221351A (en) | 1984-12-12 |
JPH0249341B2 true JPH0249341B2 (en) | 1990-10-29 |
Family
ID=14149007
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9585683A Expired - Lifetime JPH0249341B2 (en) | 1983-06-01 | 1983-06-01 | FUENOORUJUSHISEIKEIZAIRYO |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0249341B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0425556A (en) * | 1990-05-21 | 1992-01-29 | Daiwa Taika Renga Senzoushiyo:Kk | Composite material |
JP2653593B2 (en) * | 1991-12-18 | 1997-09-17 | 住友ベークライト株式会社 | Phenolic resin composition |
-
1983
- 1983-06-01 JP JP9585683A patent/JPH0249341B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS59221351A (en) | 1984-12-12 |
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