JPS5924744A - Phenolic molding material and production thereof - Google Patents
Phenolic molding material and production thereofInfo
- Publication number
- JPS5924744A JPS5924744A JP13550182A JP13550182A JPS5924744A JP S5924744 A JPS5924744 A JP S5924744A JP 13550182 A JP13550182 A JP 13550182A JP 13550182 A JP13550182 A JP 13550182A JP S5924744 A JPS5924744 A JP S5924744A
- Authority
- JP
- Japan
- Prior art keywords
- phenolic resin
- rubber
- majority
- melamine
- fiber
- 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
- 239000012778 molding material Substances 0.000 title claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000000463 material Substances 0.000 claims abstract description 17
- 239000005011 phenolic resin Substances 0.000 claims abstract description 17
- 239000000835 fiber Substances 0.000 claims abstract description 16
- 229920001971 elastomer Polymers 0.000 claims abstract description 12
- 229920001568 phenolic resin Polymers 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 3
- 239000011256 inorganic filler Substances 0.000 claims description 7
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 7
- 238000013329 compounding Methods 0.000 claims description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 4
- 229920000459 Nitrile rubber Polymers 0.000 abstract description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 3
- 239000004677 Nylon Substances 0.000 abstract description 2
- 229920001778 nylon Polymers 0.000 abstract description 2
- 229920002635 polyurethane Polymers 0.000 abstract description 2
- 239000004814 polyurethane Substances 0.000 abstract description 2
- 239000000945 filler Substances 0.000 abstract 2
- -1 nitrile rubber Chemical compound 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 238000005299 abrasion Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 238000004898 kneading Methods 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002978 Vinylon Polymers 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- 239000006082 mold release agent Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003739 xylenols Chemical class 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はクラッチ用材料、ブレーキ用材料等に用いられ
るフェノール樹脂成形材料およびその製造方法に関する
もので、その目的とするところはアスペスト公害を発生
させるアスペストを使用することなくクラッチ用材料や
ブレーキ用材料に用いられるフェノール樹脂成形材料を
提供することにある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a phenolic resin molding material used for clutch materials, brake materials, etc., and a method for producing the same. The purpose of the present invention is to provide a phenolic resin molding material used for clutch materials and brake materials.
従来のクラッチ用材料やブレーキ用材料に用いられるフ
ェノール樹脂成形材料にアスペストが多使用されており
成形材料製造行程、成形工程、加工行程、使用中の全過
程でアスペスト公害を発生させていたものである。Conventional phenolic resin molding materials used in clutch materials and brake materials contain a large amount of aspest, which generates aspest pollution during the entire process of manufacturing, molding, processing, and use of the molding materials. be.
本発明は上記欠点を解決するもので、メラミン変性フェ
ノール樹脂、ゴム、有機繊維の8成分量が等量で全量の
過半数を占め、且つ残量の過半数が無機充填剤である組
成のフェノール樹脂成形材料であり更に上記材料を混合
後、ニーダー混練し必要によりフ造粒化することによっ
て得られる成形材料のためアスペストを全く使用するこ
となくクラッチ用材料、ブレーキ用材料等に用いること
ができるのでアスペスト公害を解消することができたも
のである。The present invention solves the above-mentioned drawbacks, and is a phenolic resin molding having a composition in which the eight components of melamine-modified phenolic resin, rubber, and organic fiber are equal in amount and account for a majority of the total amount, and the remaining amount is an inorganic filler. Aspest is a molding material obtained by mixing the above materials, kneading it in a kneader, and granulating it if necessary, so it can be used for clutch materials, brake materials, etc. without using Aspest at all. It was possible to eliminate pollution.
以下本発明を詳細に説明する。本発明に用いるメラミン
変性フェノール樹脂はレゾール型、ノボラック型各れで
もよく、又、メラミン変性クレゾ一ル樹脂、メラミン変
性キシレノール樹脂をも含み、更に糖蜜、リグニン、キ
シレン、ナフタリン、石油系芳香族炭化水素樹脂等によ
るメラミン変性フェノール樹脂等をも含むものである。The present invention will be explained in detail below. The melamine-modified phenolic resin used in the present invention may be either a resol type or a novolak type, and also includes melamine-modified cresol resin, melamine-modified xylenol resin, and further includes molasses, lignin, xylene, naphthalene, and carbonized petroleum aromatic resins. It also includes melamine-modified phenol resins made from hydrogen resins and the like.
ゴムはニトリルゴム等のようにフェノール樹脂と相溶性
のあるゴムならばよく特に限定するものではない。The rubber is not particularly limited as long as it is compatible with the phenol resin, such as nitrile rubber.
有機繊維としてはナイロン、ビニロン、ポリエステル、
ポリウレタン等のように耐熱性のある有機繊維であるな
らばよく特に限定するものではない。Organic fibers include nylon, vinylon, polyester,
There is no particular limitation as long as it is a heat-resistant organic fiber such as polyurethane.
無機充填剤としては炭酸カルシウム、シリカ、炭酸マグ
ネシウム、クレー等が用いられ特に限定するものではな
い。メラミン変性フェノール樹脂、ゴム、有機繊維、無
機充填剤以外の配合材料としては一般に用いられている
硬化剤、離型剤、着色剤等をそのまま用いることができ
る。メラミン変性フェノール樹脂、ゴム、有機繊維の量
は夫々等量であることが必要で全量の過半数を占めてい
ることが必要である。即ち樹脂量が不足すると強度不足
になり、過剰になると摩耗性が大となる。又ゴム量が不
足すると摩耗性が大となり、過剰になると強度不足にな
る。更に有機繊維量が不足すると摩耗性が大となり過剰
になると強度バラツキが発生する。樹脂、ゴム、有機繊
維の8成分量が全量の過半数を割ると摩耗性が大となり
強度も不足する。加えて無機充填剤は樹脂、ゴム、有機
繊維の8成分を除いた残量の過半数を占めることが必要
である。即ち無機充填剤量が不足すると耐熱性、成形性
が低下するからである。本発明の製造方法としては上記
配合材料中の有機繊維を切断、粉砕、粉末化してしまわ
ないことが重要でこのため従来、フェノール樹脂成形材
料製造工程で用いられているロール混練、押出機混練等
の方法は繊維を切断するため用いられず、ニーダー混練
して成形材料とするものである。この際、必要に応じて
ヘンシエルミキサー等で造粒化することもできるもので
ある。As the inorganic filler, calcium carbonate, silica, magnesium carbonate, clay, etc. can be used, but there are no particular limitations. As compounding materials other than the melamine-modified phenol resin, rubber, organic fibers, and inorganic fillers, commonly used curing agents, mold release agents, coloring agents, etc. can be used as they are. The amounts of the melamine-modified phenol resin, rubber, and organic fiber must be equal, and must account for more than half of the total amount. That is, if the amount of resin is insufficient, the strength will be insufficient, and if the amount is excessive, the abrasion will be increased. Also, if the amount of rubber is insufficient, abrasion will be high, and if it is excessive, the strength will be insufficient. Furthermore, if the amount of organic fiber is insufficient, abrasion will be high, and if it is excessive, strength variations will occur. If the amount of the eight components (resin, rubber, and organic fiber) is less than the majority of the total amount, the abrasion will be high and the strength will be insufficient. In addition, it is necessary that the inorganic filler accounts for the majority of the remaining amount excluding the eight components of resin, rubber, and organic fiber. That is, if the amount of inorganic filler is insufficient, heat resistance and moldability will decrease. In the manufacturing method of the present invention, it is important not to cut, crush, or powderize the organic fibers in the above-mentioned compounded materials.For this reason, roll kneading, extruder kneading, etc., which are conventionally used in the manufacturing process of phenolic resin molding materials, etc. This method is not used to cut the fibers, but rather kneads them with a kneader to form a molding material. At this time, granulation can be carried out using a Henschel mixer or the like, if necessary.
以下本発明の方法を実施例、従来例にもとずいて説明す
る。The method of the present invention will be explained below based on examples and conventional examples.
実施例例
メラミン変性フェノール樹脂20重量部(以下単に部と
記す)に対しニトリルゴム20部、ビニロン繊維20部
、炭酸カルシウム30部、ヘキサミン4部、離型剤2部
、着色剤2部、分散助剤2部を加えニーダーで30分間
混練してからヘンシエルミキサーで造粒化してフェノー
ル樹脂成形材料を得た。Examples 20 parts by weight of melamine-modified phenol resin (hereinafter simply referred to as parts), 20 parts of nitrile rubber, 20 parts of vinylon fiber, 30 parts of calcium carbonate, 4 parts of hexamine, 2 parts of mold release agent, 2 parts of colorant, dispersion. Two parts of the auxiliary agent were added and kneaded for 30 minutes using a kneader, followed by granulation using a Henschel mixer to obtain a phenolic resin molding material.
従来例
樹脂含量50重量%のフェノール樹脂ワニスをアスペス
トロープに含浸、乾燥させてロープ状プリプレグを得た
。Conventional Example Aspestrope was impregnated with a phenolic resin varnish having a resin content of 50% by weight and dried to obtain a rope-like prepreg.
実施例及び従来例の成形材料及びプリプレグを成形圧力
100kg/cm3、成形温度155℃で2分間成形し
て円板状のクラッチ材成形品を得、試験した結果は第1
表で明白なように本発明のフェノール樹脂成形材料およ
びその製造方法から得られた成形品の100℃及び20
0℃における摩耗率はアスペストを含有していないにも
かかわらずアスペスト含有品と同等で本発明のフェノー
ル樹脂成形材料およびその製造方法の優れていることを
確認した。The molding materials and prepregs of the examples and conventional examples were molded for 2 minutes at a molding pressure of 100 kg/cm3 and a molding temperature of 155°C to obtain a disc-shaped clutch material molded product.
As is clear from the table, the molded products obtained from the phenolic resin molding material of the present invention and the method for producing the same at 100°C and 20°C
The wear rate at 0° C. was equivalent to that of a product containing aspest even though it did not contain aspest, confirming the superiority of the phenolic resin molding material of the present invention and its manufacturing method.
Claims (2)
8成分量が等量で全量の過半数を占め、且つ残量の過半
数が無機充填剤であることを特徴とするフェノール樹脂
成形材料。(1) A phenolic resin molding material characterized in that eight components, melamine-modified phenolic resin, rubber, and organic fiber, are present in equal amounts and account for a majority of the total amount, and the majority of the remaining amount is an inorganic filler.
8成分量が等量で全量の過半数を占め,且つ残量の過半
数が無機充填剤である配合材料を混合後,ニーダー混練
し必要により造粒化することを特徴とするフェノール樹
脂の製造方法。(2) After mixing the compounding materials in which the eight components of melamine-modified phenolic resin, rubber, and organic fiber are equal in amount and account for a majority of the total amount, and the remaining amount is an inorganic filler, the mixture is kneaded with a kneader and granulated if necessary. A method for producing a phenolic resin, characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13550182A JPS5924744A (en) | 1982-08-02 | 1982-08-02 | Phenolic molding material and production thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13550182A JPS5924744A (en) | 1982-08-02 | 1982-08-02 | Phenolic molding material and production thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5924744A true JPS5924744A (en) | 1984-02-08 |
Family
ID=15153223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13550182A Pending JPS5924744A (en) | 1982-08-02 | 1982-08-02 | Phenolic molding material and production thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5924744A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62109860A (en) * | 1985-11-07 | 1987-05-21 | Akebono Brake Res & Dev Center Ltd | Organic friction material |
| JPS638441A (en) * | 1986-06-28 | 1988-01-14 | Kyushu Shinko Rubber Kk | Production of anti-slip rubber material |
| US4914414A (en) * | 1989-08-03 | 1990-04-03 | Susumu Ubukata | Thermally responsive switch |
-
1982
- 1982-08-02 JP JP13550182A patent/JPS5924744A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62109860A (en) * | 1985-11-07 | 1987-05-21 | Akebono Brake Res & Dev Center Ltd | Organic friction material |
| JPS638441A (en) * | 1986-06-28 | 1988-01-14 | Kyushu Shinko Rubber Kk | Production of anti-slip rubber material |
| US4914414A (en) * | 1989-08-03 | 1990-04-03 | Susumu Ubukata | Thermally responsive switch |
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