JPH08302158A - Phenol resin molding material - Google Patents

Phenol resin molding material

Info

Publication number
JPH08302158A
JPH08302158A JP10435395A JP10435395A JPH08302158A JP H08302158 A JPH08302158 A JP H08302158A JP 10435395 A JP10435395 A JP 10435395A JP 10435395 A JP10435395 A JP 10435395A JP H08302158 A JPH08302158 A JP H08302158A
Authority
JP
Japan
Prior art keywords
phenol resin
molding material
molding
resin molding
parts
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
Application number
JP10435395A
Other languages
Japanese (ja)
Inventor
Chitoshi Yamashita
千俊 山下
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP10435395A priority Critical patent/JPH08302158A/en
Publication of JPH08302158A publication Critical patent/JPH08302158A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE: To obtain a phenol resin molding material which can be molded under a pressure lower than that for molding a commercially available phenol resin molding material and which enables both a satisfactory mold filling in the molding step and prevention of molding flash. CONSTITUTION: This molding material essentially comprises a novolak phenol resin having an ortho-para ratio of 1.0-2.5 and a soln. viscosity (in the 50% ethanolic soln. by the Ostwald method at 25 deg.C) of (20-70)×10<-6> m<2> /sec, hexamethylenetetramine, and a filler.

Description

【発明の詳細な説明】Detailed Description of the Invention 【産業上の利用分野】[Industrial applications]

【0001】本発明は低圧成形性及び硬化性に優れ、か
つ成形時のバリの発生が極めて少ないフェノール樹脂成
形材料に関するものである。
The present invention relates to a phenol resin molding material which is excellent in low-pressure moldability and curability and has very few burrs during molding.

【0002】[0002]

【従来の技術】従来からフェノール樹脂成形材料は、耐
熱性、電気特性、機械的強度等の諸特性が優れ、良好な
成形性を有するとともに、安価に得られることから種々
の用途に用いられている。
2. Description of the Related Art Conventionally, phenol resin molding materials have been used for various purposes because they are excellent in various properties such as heat resistance, electrical characteristics and mechanical strength, have good moldability and can be obtained at low cost. There is.

【0003】フェノール樹脂成形材料は一般に射出成形
が行なわれており、金型キャビティに高圧で成形材料を
注入し、一定時間圧力をかけながら硬化し賦形を行なっ
ている。従って金型内に賦形された成形品中に残留応力
が発生し、金型から取出された後の冷却過程において、
この残留応力が拡散するときに成形品に反りや変形を生
ずることがある。また、金型キャビティに高圧で成形材
料を注入するため、金型の微小な変形により金型間に隙
間ができ、それに伴いバリも多く発生する。
Generally, a phenol resin molding material is injection-molded, and the molding material is injected into the mold cavity at a high pressure, and is cured by applying pressure for a certain period of time to perform shaping. Therefore, residual stress occurs in the molded product shaped in the mold, and in the cooling process after being removed from the mold,
When the residual stress diffuses, the molded product may be warped or deformed. Further, since the molding material is injected into the mold cavity at a high pressure, a minute deformation of the mold creates a gap between the molds, which causes a lot of burrs.

【0004】従来、これらの問題点を解決する方法とし
て成形材料の溶融粘度の低下、即ち流動性を良好にして
射出圧力を低くすることが行なわれる(例えば、特開平
5−156120号公報に記載)が、バリの発生は少な
いものの成形材料の硬化が遅くなるので、成形サイクル
が長くなり、実用に供することは困難である。
Conventionally, as a method for solving these problems, the melt viscosity of the molding material is lowered, that is, the fluidity is improved and the injection pressure is lowered (for example, described in JP-A-5-156120). However, since the curing of the molding material is delayed, the molding cycle becomes long and it is difficult to put it into practical use.

【0005】[0005]

【発明が解決しようとする課題】本発明は、低圧成形す
ることができ、且つ硬化の速いフェノール樹脂成形材料
を得るため、種々検討した結果完成されたものであり、
その目的とするところは低圧の成形において金型への充
填性及び硬化性に優れ、成形時のバリの発生が極めて少
ないフェノール樹脂成形材料を提供するところにある。
SUMMARY OF THE INVENTION The present invention has been completed as a result of various studies in order to obtain a phenol resin molding material capable of low-pressure molding and having a fast curing,
It is an object of the invention to provide a phenol resin molding material which is excellent in mold filling property and curability in low-pressure molding and has very few burrs during molding.

【0006】[0006]

【課題を解決するための手段】本発明は、オルソ・パラ
比が1.0〜2.5の範囲にあり、溶液粘度(50%エ
タノール溶液、オストワルド法(25℃)、以下同じ測
定法)が(20〜70)×10-62/secであるノボラ
ック型フェノール樹脂とヘキサメチレンテトラミン(以
下、ヘキサミンという)と充填剤とを必須成分とするこ
とを特徴とするフェノール樹脂成形材料である。
According to the present invention, the ortho-para ratio is in the range of 1.0 to 2.5, and the solution viscosity (50% ethanol solution, Ostwald method (25 ° C), the same measurement method hereinafter). Is a (20 to 70) × 10 −6 m 2 / sec novolac type phenolic resin, hexamethylenetetramine (hereinafter referred to as “hexamine”) and a filler as essential components. .

【0007】本発明において、用いられるフェノール樹
脂は、フェノール樹脂成形材料に、射出成形時の可塑化
において速やかに溶融して低粘度となり、低圧で成形で
きる特性を付与するために用いられ、更には、このフェ
ノール樹脂は高温では速硬化であるため成形サイクルを
短縮することを可能とする。従来のノボラック樹脂の溶
液粘度は(80〜300)×10-62/secであり、射
出成形時の可塑化で低圧で成形可能となるのに十分な低
粘度となる特性を成形材料に付与することができない。
The phenolic resin used in the present invention is used for imparting to the phenolic resin molding material the characteristic that it is rapidly melted to have a low viscosity during plasticization during injection molding and can be molded at a low pressure. Since this phenolic resin cures rapidly at high temperatures, it makes it possible to shorten the molding cycle. The conventional novolak resin has a solution viscosity of (80 to 300) × 10 -6 m 2 / sec, and the molding material has the property of low viscosity sufficient to enable low-pressure molding by plasticization during injection molding. Cannot be granted.

【0008】本発明に用いられるノボラック型フェノー
ル樹脂の溶液粘度は(20〜70)×10-62/secで
ある。20より小さいと樹脂が常温で液状化しやすく、
樹脂の保管及び成形材料の製造化に難がある。70より
大きいと射出成形時の可塑化で低圧で成形可能となるの
に十分な低粘度となる特性を成形材料に付与することが
できない。
The solution viscosity of the novolac type phenol resin used in the present invention is (20 to 70) × 10 -6 m 2 / sec. If it is less than 20, the resin tends to liquefy at room temperature,
There are difficulties in storing the resin and manufacturing the molding material. When it is more than 70, the molding material cannot be provided with a property that the viscosity is low enough to enable molding at low pressure due to plasticization during injection molding.

【0009】本発明のフェノール樹脂成形材料におい
て、硬化剤であるヘキサミンの配合割合はフェノール樹
脂成分に対して7〜25重量%、好ましくは10〜20
重量%である。7重量%より少ないと硬化が十分に行な
われず、25重量%より多くても硬化性は改善されず、
逆に成形品特性(例えは、機械的強度)が低下する。
In the phenol resin molding material of the present invention, the compounding ratio of hexamine as a curing agent is 7 to 25% by weight, preferably 10 to 20% by weight based on the phenol resin component.
% By weight. If it is less than 7% by weight, curing will not be sufficiently performed, and if it is more than 25% by weight, curability will not be improved.
On the contrary, the characteristics of the molded product (for example, mechanical strength) are deteriorated.

【0010】本発明のフェノール樹脂成形材料に用いら
れる充填剤としては、木粉、パルプ粉、各種織物粉砕
物、或いはフェノール樹脂積層板・成形品等の粉砕粉等
の有機質のもの、シリカ、アルミナ、水酸化アルミニウ
ム、ガラス、タルク、クレー、マイカ、炭酸カルシウ
ム、カーボン等の無機質の粉末のもの、ガラス繊維、ガ
ーボン繊維、アスベスト等の無機質繊維等の1種以上を
用いることができる。
The filler used in the phenol resin molding material of the present invention includes wood powder, pulp powder, various pulverized woven materials, organic materials such as pulverized powder of phenol resin laminated plates and molded products, silica, alumina. One or more of inorganic powders such as aluminum hydroxide, glass, talc, clay, mica, calcium carbonate and carbon, and inorganic fibers such as glass fiber, garbon fiber and asbestos can be used.

【0011】本発明のフェノール樹脂成形材料中の配合
割合は、ヘキサミンを含むフェノール樹脂が20〜70
重量%、充填剤が80〜30重量%である。また、本発
明のフェノール樹脂成形材料には、更に滑剤、溶剤、着
色剤、硬化促進剤、難燃剤等の各種の添加剤を適宜配合
することができる。
The blending ratio of the phenol resin molding material of the present invention is such that the phenol resin containing hexamine is 20 to 70.
% By weight and 80 to 30% by weight of filler. Further, various additives such as a lubricant, a solvent, a colorant, a curing accelerator, and a flame retardant can be appropriately added to the phenol resin molding material of the present invention.

【0012】[0012]

【作用】本発明は、ノボラック型フェノール樹脂が溶融
時低粘度であるため、フェノール樹脂成形材料が成形時
の可塑化工程で極めて速やかに溶融して低粘度となり、
良好な流動性を有することにより、余分な圧力を加える
ことなく低圧で金型のキャビティ内に充填することがで
き、速やかに硬化することにより成形時のバリの発生を
極めて少なくすることができ、又良好な特性を有する成
形品を得ることができる。更に、成形サイクルの短縮、
バリが少ないことによる金型摩耗の軽減・金型寿命の向
上、低圧成形による金型軽量化等を達成することができ
る。
In the present invention, since the novolac type phenolic resin has a low viscosity when melted, the phenolic resin molding material melts very quickly in the plasticizing step at the time of molding to have a low viscosity,
By having good fluidity, it is possible to fill the cavity of the mold at low pressure without applying extra pressure, and it is possible to extremely reduce the occurrence of burrs during molding due to rapid curing. Also, a molded product having good characteristics can be obtained. Furthermore, shortening the molding cycle,
It is possible to reduce die wear due to less burr, improve die life, and reduce die weight by low-pressure molding.

【0013】[0013]

【実施例】以下に、実施例と比較例により本発明を説明
する。ここにおいて「部」は重量部を表す。
EXAMPLES The present invention will be described below with reference to Examples and Comparative Examples. Here, "parts" represent parts by weight.

【0014】《実施例1》オルソ・パラ比が1.5であ
るノボラック型フェノール樹脂(溶液粘度30×10-6
2/sec、重量平均分子量500)45部、ヘキサミン
7部、水酸化カルシウム3部、木粉30部、炭酸カルシ
ウム10部、離型剤、顔料を5部を混合し、2本ロール
ミルを用いて加熱混練し、冷却後粉砕してフェノール樹
脂成形材料を得た。
Example 1 A novolac type phenol resin having an ortho-para ratio of 1.5 (solution viscosity 30 × 10 -6
m 2 / sec, weight average molecular weight 500) 45 parts, hexamine 7 parts, calcium hydroxide 3 parts, wood powder 30 parts, calcium carbonate 10 parts, mold release agent, and pigment 5 parts are mixed and a two-roll mill is used. The mixture was heated and kneaded, cooled, and pulverized to obtain a phenol resin molding material.

【0015】《実施例2》オルソ・パラ比が2.0であ
るノボラック型フェノール樹脂(溶液粘度50×10-6
2/sec、重量平均分子量750)45部、ヘキサミン
7部、水酸化カルシウム3部、木粉30部、炭酸カルシ
ウム10部、離型剤、顔料及び溶剤を5部混合した。こ
の他は実施例1と同様にしてフェノール樹脂成形材料を
得た。
Example 2 A novolac type phenol resin having an ortho-para ratio of 2.0 (solution viscosity 50 × 10 -6
m 2 / sec, weight average molecular weight 750) 45 parts, hexamine 7 parts, calcium hydroxide 3 parts, wood powder 30 parts, calcium carbonate 10 parts, a release agent, a pigment and a solvent 5 parts were mixed. A phenol resin molding material was obtained in the same manner as in Example 1 except for the above.

【0016】《比較例1及び2》オルソ・パラ比が1.
5であるノボラック型フェノール樹脂(溶液粘度100
×10-62/sec、重量平均分子量2000)45部、
ヘキサミン7部、水酸化カルシウム3部、木粉30部、
離型剤、顔料を5部を混合した。この他は実施例1と同
様にしてフェノール樹脂成形材料を得た。
Comparative Examples 1 and 2 The ortho-para ratio is 1.
Novolak type phenolic resin of 5 (solution viscosity 100
× 10 -6 m 2 / sec, weight average molecular weight 2000) 45 parts,
Hexamine 7 parts, calcium hydroxide 3 parts, wood flour 30 parts,
5 parts of the release agent and the pigment were mixed. A phenol resin molding material was obtained in the same manner as in Example 1 except for the above.

【0017】実施例及び比較例で用いたフェノール樹脂
の粘度およびフェノール樹脂成形材料の特性及びをバリ
取り仕上げ後に成形品に残ったバリ量を表1に示す。な
お、比較例において、比較例1は実施例と同じゲージ圧
50kg/cm2 で成形した場合であり、比較例2はゲージ
圧を110kg/cm2 に高くして成形した場合である。表
1の結果から明らかなように、各実施例で得られたフェ
ノール樹脂成形材料は低粘度であり、硬化性が優れてい
る。そして、充填性が良好で成形時のバリの発生が極め
て少ないことがわかる。
Table 1 shows the viscosity of the phenol resin used in the examples and comparative examples, the characteristics of the phenol resin molding material, and the amount of burr remaining in the molded product after deburring. In Comparative Examples, Comparative Example 1 is a case of molding with the same gauge pressure of 50 kg / cm 2 , and Comparative Example 2 is a case of increasing the gauge pressure to 110 kg / cm 2 . As is clear from the results in Table 1, the phenolic resin molding materials obtained in the respective examples have low viscosity and excellent curability. It can be seen that the filling property is good and the occurrence of burrs during molding is extremely small.

【0018】[0018]

【表1】 [Table 1]

【0019】表1における特性の測定方法は次の通りで
ある。 1.成形材料の流動性:高化式フローテスター(島津製
作所製、CFT-500C)によって測定した溶融粘度を示し
た。 2.硬化性:100℃に予熱された成形材料をトランス
ファー成形機で175℃の金型に充填し30秒後に成形
品を取出し、更に10秒経過した後のバーコル硬度を示
した。 3.成形性:射出成形機で円盤(50φ×厚さ3mm)
を成形し、キャビティヘの充填性及びエアベントにおけ
るバリ発生を目視で判定した。
The method of measuring the characteristics in Table 1 is as follows. 1. Flowability of molding material: The melt viscosity measured by a Koka type flow tester (CFT-500C manufactured by Shimadzu Corporation) is shown. 2. Curability: The molding material preheated to 100 ° C. was charged into a mold at 175 ° C. by a transfer molding machine, the molded product was taken out after 30 seconds, and the Barcol hardness after 10 seconds was shown. 3. Moldability: Disc by injection molding machine (50φ x thickness 3mm)
Was molded, and the filling property into the cavity and the occurrence of burrs in the air vent were visually determined.

【0020】[0020]

【発明の効果】本発明のフェノール樹脂成形材料は、溶
融時には低粘度であり、金型温度では硬化性に優れてい
るので、低圧成形が可能であり、成形時の金型への充填
性とバリ発生の抑制を両立することができる。従って、
成形性の優れたフェノール樹脂成形材料として幅広い利
用が可能であり、成形サイクルの短縮、金型寿命の向上
が達成できる。
EFFECTS OF THE INVENTION The phenol resin molding material of the present invention has a low viscosity when melted and is excellent in curability at the mold temperature, so that low pressure molding is possible, and the mold filling property during molding is improved. It is possible to achieve both suppression of burr generation. Therefore,
It can be widely used as a phenolic resin molding material with excellent moldability, shortening the molding cycle and improving the mold life.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 オルソ・パラ比が1.0〜2.5の範囲に
あり、溶液粘度(50%エタノール溶液、オストワルド
法(25℃))が(20〜70)×10-62/sec で
あるノボラック型フェノール樹脂とヘキサメチレンテト
ラミンと充填剤とを必須成分とすることを特徴とするフ
ェノール樹脂成形材料。
1. The ortho-para ratio is in the range of 1.0 to 2.5, and the solution viscosity (50% ethanol solution, Ostwald method (25 ° C.)) is (20 to 70) × 10 −6 m 2 / A phenol resin molding material comprising a novolac-type phenol resin having a sec, hexamethylenetetramine, and a filler as essential components.
JP10435395A 1995-04-27 1995-04-27 Phenol resin molding material Pending JPH08302158A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10435395A JPH08302158A (en) 1995-04-27 1995-04-27 Phenol resin molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10435395A JPH08302158A (en) 1995-04-27 1995-04-27 Phenol resin molding material

Publications (1)

Publication Number Publication Date
JPH08302158A true JPH08302158A (en) 1996-11-19

Family

ID=14378521

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10435395A Pending JPH08302158A (en) 1995-04-27 1995-04-27 Phenol resin molding material

Country Status (1)

Country Link
JP (1) JPH08302158A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7541410B2 (en) 2004-12-27 2009-06-02 Sumitomo Bakelite Co., Ltd. Thermosetting resin composition, thermosetting resin molding compound and cured product thereof
US10144823B2 (en) 2014-05-30 2018-12-04 Sumitomo Bakelite Co., Ltd. Phenolic resin composition and phenolic resin cured product

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7541410B2 (en) 2004-12-27 2009-06-02 Sumitomo Bakelite Co., Ltd. Thermosetting resin composition, thermosetting resin molding compound and cured product thereof
US10144823B2 (en) 2014-05-30 2018-12-04 Sumitomo Bakelite Co., Ltd. Phenolic resin composition and phenolic resin cured product

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