JPS59105048A - Phenolic resin molding material - Google Patents

Phenolic resin molding material

Info

Publication number
JPS59105048A
JPS59105048A JP21392182A JP21392182A JPS59105048A JP S59105048 A JPS59105048 A JP S59105048A JP 21392182 A JP21392182 A JP 21392182A JP 21392182 A JP21392182 A JP 21392182A JP S59105048 A JPS59105048 A JP S59105048A
Authority
JP
Japan
Prior art keywords
phenolic resin
molding material
resin
xylene
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.)
Granted
Application number
JP21392182A
Other languages
Japanese (ja)
Other versions
JPH0432865B2 (en
Inventor
Tsutomu Nagata
勉 永田
Yoichi Nagata
洋一 永田
Toshio Mayama
間山 歳夫
Mitsuo Ito
光生 伊藤
Masanori Kokubo
小久保 正典
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toshiba Chemical Products Co Ltd
Kyocera Chemical Corp
Original Assignee
Toshiba Chemical Products Co Ltd
Toshiba Chemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toshiba Chemical Products Co Ltd, Toshiba Chemical Corp filed Critical Toshiba Chemical Products Co Ltd
Priority to JP21392182A priority Critical patent/JPS59105048A/en
Publication of JPS59105048A publication Critical patent/JPS59105048A/en
Publication of JPH0432865B2 publication Critical patent/JPH0432865B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To provide the titled molding material having well-balanced properties, for example, having high heat resistance and mechanical strength and excellent in wear resistance and electrical characteristics, consisting mainly of a phenolic resin, a xylene resin, glass fiber, natural org. fiber and kaolin clay. CONSTITUTION:A phenolic resin, a xylene resin or a xylene-modified phenolic resin, 5-40wt%, pref. 15-25wt% glass fiber, 5-30wt%, pref, 8-20wt% natural org. fiber and 5-30wt. kaolin clay are blended together as main ingredients to obtain the desired phenolic resin molding material, each quantity being based on that of the molding material. If desired, additives such as hardener, colorant, flame retarder, plasticizer, etc. may be added.

Description

【発明の詳細な説明】 [発明の技術分野] 本発明は、耐熱性、機械的強度、耐摩耗性、J5よび電
気特性に優れたフェノール樹脂成形材料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a phenolic resin molding material excellent in heat resistance, mechanical strength, abrasion resistance, J5 and electrical properties.

[発明の技術的背景とその問題点コ ツエノール樹脂は、充填剤、可塑剤、着色剤、離形剤等
を混合、混練した成形材オ′≧1としC幅広く使用され
ている。
[Technical background of the invention and its problems Cotenol resin is widely used as a molding material prepared by mixing and kneading fillers, plasticizers, colorants, mold release agents, etc.

一般的にフェノール樹脂成形材Δ″31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
摩耗性等に欠点があった。 この欠点を改良するものと
しでアスベスト、1夫酸カルシウム、およびタルク等の
無(幾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d3よび耐摩耗性に
難点がある。 この難点を改良しようとグラノIイトを
充枦剤として用いたものがあるが耐摩耗性につい]よ改
良されるものの機械的強度、電気特性に欠5、Jがある
。 これらの欠点を改良しようと刀うス繊ff−ff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)に欠点があった。
In general, phenolic resin molding material Δ''31 uses wood flour as the main filler, so it has drawbacks in heat resistance, mechanical strength, abrasion resistance, etc. To improve these drawbacks, asbestos, There are products that use calcium monoaltate, talc, and other substances as fillers. Although this improves heat resistance, it has drawbacks in mechanical strength d3 and abrasion resistance. Let's try to improve this drawback. There are fabrics using granoite and granoite as fillers, but although they improve wear resistance, they lack mechanical strength and electrical properties. Those using ff-ff as a filler have high heat resistance and mechanical strength, but have a drawback in abrasion resistance (particularly abrasion of the mating metal material).

 又、天然有IMlaNを充Ji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点が
ある。 このような状況で優れた耐熱性、機械的強度、
耐摩耗1’1. 、 d、’;よび電気特性をイjし1
=バランスのとれたフェノール樹脂成形拐第1が求めら
れていノこ、。
In addition, those using natural IMlaN as a JI filler have good mechanical strength and wear resistance, but have a drawback in heat resistance. Excellent heat resistance, mechanical strength,
Wear resistance 1'1. , d,'; and the electrical characteristics are 1
= A well-balanced phenolic resin molding saw is in demand.

[発明の目的] 本発明は、上記の欠点を解消づ−る耐熱性、機械的強度
、耐摩耗性d′3よび電気特性に優れたバランスのどれ
だフェノール樹脂成形4A利を捉供づ−ることを目的ど
している。
[Object of the Invention] The present invention provides a phenolic resin molding method 4A that has an excellent balance of heat resistance, mechanical strength, abrasion resistance d'3, and electrical properties that eliminates the above-mentioned drawbacks. The purpose is to

「発明の概要J 本発明は、上記の目的を達成づべく鋭意研究を重ね7j
結果、次に示す成形材料が上記目的としている特1うを
有していることを見い出したものである。
“Summary of the Invention J The present invention was developed through intensive research to achieve the above object.
As a result, it has been discovered that the following molding material has the above-mentioned objective characteristics.

即ら、本発明は、(a )フェノール樹脂、(b、)キ
シレン樹脂若しくはキシレン変性71ノール樹脂、(C
)カラス繊キ(f、(d )天然有機繊維1、(e)カ
オリンクレーを主成分とすることを特徴とづ′るフェノ
ール樹脂成形月利で、成形材料に対し/ T: 力’ 
7 ス4Ilill’[5〜40 重量 %、天rA 
′5S tjW Xt% lit 5〜30重量%およ
び力Aリンクレー5へ・30申崖%を含有するものが特
に、耐熱1?1.ぼ械的強度、耐摩耗性および電気特性
に優れたバランスのとれたフェノール樹脂成形月利であ
る。
That is, the present invention provides (a) a phenolic resin, (b) a xylene resin or a xylene-modified 71-nor resin, (C
) Grass fiber (f, (d) Natural organic fiber 1, (e) Phenol resin molding rate, which is characterized by having kaolin clay as the main component, relative to the molding material / T: Force'
7 Su4Illill' [5-40% by weight, TenrA
'5S tjW It is a well-balanced phenolic resin molding product with excellent mechanical strength, abrasion resistance, and electrical properties.

本発明に使用するフェノール樹脂は、フェノール、クレ
ゾール等のフェノール類、又す糖蜜、リグニン、キシレ
ン、ナフタレン、Gd系芳香族炭化水素による変性)1
ノール類と、ノj・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μIこノボ
ラック型フ5ノール樹脂初期縮合物、又はレゾール型ノ
エノール樹脂初朋縮合物およびノボラック型フ」ノール
樹脂初期縮合物とレゾール型71ノール(ひI脂辺明縮
含物を組み合わせた一bの等が挙げlうれる。
The phenolic resin used in the present invention is modified with phenols such as phenol and cresol, or molasses, lignin, xylene, naphthalene, and Gd-based aromatic hydrocarbons.
The novolac type phenol resin initial condensate, or the resol type noenol resin Hatsuho condensate and the novolac are produced by blending the nols, noj rumin, and paraformaldehyde in an appropriate molar ratio and reacting them under a catalyst. Examples include 1b, which is a combination of a type phenol resin precondensate and a resol type 71nol (I fatty acid condensate).

本発明で使用づるキシレン樹脂若しくはキシレン変性フ
ェノール樹脂としCは、−1シレンホルムアルデヒド樹
脂又はキシレンボルムアルデヒド4カ1脂をフェノール
もしくはアルキルノ■−ノールと反応させたキシレン変
性71ノール樹脂等が挙(yられる。
Examples of the xylene resin or xylene-modified phenol resin used in the present invention (C) include xylene-modified 71-nol resins made by reacting -1 silene formaldehyde resin or xylene formaldehyde 4-1 fat with phenol or alkylno-nol. It will be done.

本発明で使用リ−るガラス楳肩1としては、2〜20μ
径の単繊維が収束されたス1−ランドをo、1〜25m
mに切断したーしの等が挙げられる。
The glass shoulder 1 used in the present invention is 2 to 20 μm.
A land in which single fibers of diameter are converged is o, 1 to 25 m.
Examples include ``Shino'' cut into m.

又、本発明に使用する天然有機繊維としては、綿フロッ
ク、α−レルロース、亜麻、大麻、1【1麻、綿織布、
綿毛わ)、等ノ)(挙げられる。
In addition, the natural organic fibers used in the present invention include cotton flock, α-lerulose, flax, hemp, 1[1 linen, cotton woven fabric,
Fluff), etc.) (included).

更に本発明で使用覆る力Δ−リンクレーとしては、乾式
分級カオリンクレー、酸性含水カオリンクレー、中性含
水カオリンクレー、焼成カオリンクレー、サー七Aブヂ
ックカΔリンクレー等が挙げられる。
Further, examples of the power Δ-link clay used in the present invention include dry classified kaolin clay, acidic hydrated kaolin clay, neutral hydrated kaolin clay, calcined kaolin clay, and Sir 7A Budik Δ-link clay.

上jホの如く、本発明は、フェノール樹脂、キシレン樹
脂又はキシレン変性フェノール樹脂、ガラス繊維、天然
有機繊維d3よびカオリンクレーを主成分とする71ノ
ール樹脂成形材3′+1であるが各成分の配合割合を次
に説、明する。
As described above, the present invention is a 71-nor resin molding material 3'+1 whose main components are phenol resin, xylene resin or xylene-modified phenol resin, glass fiber, natural organic fiber d3, and kaolin clay. The blending ratio will be explained and explained below.

ガラス繊維の配合割合は、成形材料に対して5〜40重
量%配合される。 5車m%未満では機械的強度が弱く
好ましくない。  40手1%を超えると耐摩耗性が悪
くなる。 より好゛ましくは、15〜25@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重昂%である。
The blending ratio of glass fiber is 5 to 40% by weight based on the molding material. If it is less than 5 m%, the mechanical strength will be weak and undesirable. If it exceeds 1% for 40 hands, the wear resistance will deteriorate. More preferably, it is 15 to 25% by weight. The blending ratio of natural organic fibers to the molding material is 5 to 5.
It is 30%.

5重量%未満では機械的強度が弱く、30重但%を超え
ると耐熱性が悪り4rる。 より好ましくは8〜20重
恒%の範囲である。
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. More preferably, it is in the range of 8 to 20%.

力Aリンクレーの配合割合は、成形材料に対して5〜3
0重量%である。 5重量%未満では耐摩耗性および耐
熱性に効果がなく、30重量%を超えると機械的強度が
劣り都合が悪い。従ってガラスtvta、天然石1m1
Jj維J3よび力Aリンクレーはそれぞれ上記範囲に限
定される。
The blending ratio of Riki A link clay is 5 to 3 to the molding material.
It is 0% by weight. If it is less than 5% by weight, there will be no effect on wear resistance and heat resistance, and if it exceeds 30% by weight, mechanical strength will be poor and this is not convenient. Therefore glass tvta, natural stone 1m1
Jj fiber J3 and force A link clay are each limited to the above ranges.

本発明の成形材131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、カップ
リング処理剤、可塑剤等の添加剤を配合することかで゛
きる。
In addition to the above, the molding material 131 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 treatment agent, a plasticizer, etc., as necessary. I can do it.

本発明のフェノール樹脂成形イΔイ′qは、通76次の
ようにして製造される。 所定Wのフェノール樹脂、キ
シレン樹脂若しくはキシレン変(’l〕Jノール樹脂、
ガラス繊維、天然有機繊維、a3よび力Aリンクレー、
必要に応じ硬化剤、着色剤、硬化促進剤、難燃剤、離形
剤、カップリング処理剤、可塑剤、を混合し、均一に分
散さUたのら、混練(;届で加熱混練し、次いで冷19
同化さけて粉砕機で適当な太ささ[こ粉砕しC)「ノー
ル樹脂成形lわ1どする。
The phenolic resin molded i.DELTA.i'q of the present invention is manufactured as follows. Phenol resin, xylene resin or xylene modified ('l)J nord resin with a specified W,
Glass fiber, natural organic fiber, A3 and A link clay,
Mix curing agent, coloring agent, curing accelerator, flame retardant, mold release agent, coupling treatment agent, plasticizer as necessary, and heat and knead until uniformly dispersed. Then cold 19
Avoid assimilation and crush to appropriate thickness using a crusher.

「発明の効果] 本発明の71ノール樹脂成形材料は、耐熱性が高く、機
械的強電が強く、耐17耗(イ1および電気特性に優れ
UJ3す、極めてバランスのとれたものである。
"Effects of the Invention" The 71-nol resin molding material of the present invention has high heat resistance, strong mechanical strength, wear resistance (17) and excellent electrical properties (UJ3), and is extremely well-balanced.

し発明の実施例」 以下、本発明を実施例により具体的に説明づるが、本発
明はこれらの実施例にJ一つ−C限定されるものではな
い。 以下「%jどは[重量%」を意味する。
EXAMPLES OF THE INVENTION The present invention will be specifically explained below with reference to Examples, but the present invention is not limited to these Examples. Hereinafter, "%j" means "% by weight".

実施例 1゜ ノボラック型フェノール樹脂40%、キシレン変性フェ
ノール樹脂5%にヘキリーメチレンア1〜ラミン7%、
ガラス繊維20%、綿フロック 10%、カオリンクレ
ー 10%その他添加剤8%を1;)温で混合し、90
〜110℃で混練して冷却したのち、粉砕してフェノー
ル樹脂成形材料を冑た。 この成形材料を圧縮成形およ
び射出成形r170℃に加熱した金型で成形硬化さ1.
IC成形品とした++  1:’Iられた成形品につい
てその特性を測定したので第′1表に示した。
Example 1゜40% novolac type phenolic resin, 5% xylene modified phenolic resin, 1 to 7% hexyl methylene amine,
Mix 20% glass fiber, 10% cotton flock, 10% kaolin clay and 8% other additives at 1;) temperature,
After kneading and cooling at ~110°C, the mixture was crushed to remove the phenolic resin molding material. This molding material was molded and hardened in a mold heated to 170°C for compression molding and injection molding.
The characteristics of the IC molded product were measured and are shown in Table '1.

実施例 2゜ レゾール型フーrノール樹脂40%、:lシレン変性フ
ェノール樹脂10%にガラスi!、1lfl 15 %
、カオリンクレー 15%、ぞの仙の添加剤5%を実施
例1と同様に操作処理してフェノール樹脂成形材料を得
た。 次いで同様に成形品となし、その特性を測定した
ので第1表に示しIC。
Example 2 40% resol type phenol resin, 10% silene modified phenolic resin and glass i! , 1lfl 15%
, 15% kaolin clay, and 5% Zonosen additive were treated in the same manner as in Example 1 to obtain a phenolic resin molding material. Next, a molded product was made in the same manner, and its characteristics were measured and are shown in Table 1.

比較例 1゜ ノボラック型フェノール樹脂50%にヘキリメヂレンテ
1ヘラミン8%、木粉35%、その他添加剤7%を実施
例1と同様に操作処理して成形材(°3]を得た。 次
いで同様に成形品として−での特性を測定したので第1
表に示した。
Comparative Example 1° A molded material (°3) was obtained by treating 50% of novolac type phenolic resin, 8% of hexylimedelente 1 heramine, 35% of wood flour, and 7% of other additives in the same manner as in Example 1. We measured the characteristics of the molded product at -, so the first
Shown in the table.

比較例 2゜ レゾール型フ」ノール484脂50%にガラス4K f
f[45%その他添加剤5%を比較例1と同様に操作処
理して成形4A斜を1!′7k。 次いて同様に成形品
どしてその特性を測定したのC第1表に示した。
Comparative example 2° resol type phenol 484 fat 50% and glass 4K f
f [45% and 5% of other additives were processed in the same manner as in Comparative Example 1 to form 4A slope 1! '7k. Next, a molded product was made in the same manner and its properties were measured, and the results are shown in Table C1.

第1表 ◎印; 特に良好 O印: 良好 Δ印; やや劣る ×印: 劣る =331Table 1 ◎ mark: Particularly good O mark: Good Δ mark; Slightly inferior ×: Inferior =331

Claims (1)

【特許請求の範囲】 1 (a)フェノール樹脂 (b)キシレン樹脂若しくはキシレン変性フェノール樹
脂 (C)ガラス繊維 (d )天然有機繊維 (e)力Aリンクレー を主成分とり゛ることを特徴とするフェノール樹脂成形
材料。 2 成形旧材に対し、ガラス繊維5〜40千m%、天然
有(幾繊紐5〜30重M%、カオリンクレー5〜30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
載のフェノール樹脂成形材料。
[Claims] 1. (a) Phenol resin (b) Xylene resin or xylene-modified phenol resin (C) Glass fiber (d) Natural organic fiber (e) A link clay as the main component. Phenolic resin molding material. 2. Claim 1, characterized in that it contains 5 to 40,000 m% of glass fiber, 5 to 30 wt. M% of natural fibers, and 5 to 30 wt.% of kaolin clay, based on the old molded material. The phenolic resin molding material described.
JP21392182A 1982-12-08 1982-12-08 Phenolic resin molding material Granted JPS59105048A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21392182A JPS59105048A (en) 1982-12-08 1982-12-08 Phenolic resin molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21392182A JPS59105048A (en) 1982-12-08 1982-12-08 Phenolic resin molding material

Publications (2)

Publication Number Publication Date
JPS59105048A true JPS59105048A (en) 1984-06-18
JPH0432865B2 JPH0432865B2 (en) 1992-06-01

Family

ID=16647242

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21392182A Granted JPS59105048A (en) 1982-12-08 1982-12-08 Phenolic resin molding material

Country Status (1)

Country Link
JP (1) JPS59105048A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10155863B2 (en) 2014-10-31 2018-12-18 Sumitomo Bakelite Co., Ltd. Phenolic resin composition and molded body
CN112708241A (en) * 2020-12-29 2021-04-27 江苏森博新材料有限公司 Ammonia-free phenolic moulding plastic and its production method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4825771A (en) * 1971-08-05 1973-04-04
JPS5335793A (en) * 1976-09-14 1978-04-03 Matsushita Electric Works Ltd Production of phenolic resin molding material

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4825771A (en) * 1971-08-05 1973-04-04
JPS5335793A (en) * 1976-09-14 1978-04-03 Matsushita Electric Works Ltd Production of phenolic resin molding material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10155863B2 (en) 2014-10-31 2018-12-18 Sumitomo Bakelite Co., Ltd. Phenolic resin composition and molded body
CN112708241A (en) * 2020-12-29 2021-04-27 江苏森博新材料有限公司 Ammonia-free phenolic moulding plastic and its production method

Also Published As

Publication number Publication date
JPH0432865B2 (en) 1992-06-01

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