JPS5924740A - Phenolic molding material - Google Patents

Phenolic molding material

Info

Publication number
JPS5924740A
JPS5924740A JP13551182A JP13551182A JPS5924740A JP S5924740 A JPS5924740 A JP S5924740A JP 13551182 A JP13551182 A JP 13551182A JP 13551182 A JP13551182 A JP 13551182A JP S5924740 A JPS5924740 A JP S5924740A
Authority
JP
Japan
Prior art keywords
phenolic
ammonium borate
molding material
resin
phenolic resins
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
JP13551182A
Other languages
Japanese (ja)
Inventor
Takashi Konya
紺谷 隆
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP13551182A priority Critical patent/JPS5924740A/en
Publication of JPS5924740A publication Critical patent/JPS5924740A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To improve injection moldability and high-temperature rigidity of moldings, by incorporating ammonium borate in a phenolic molding material. CONSTITUTION:1-19wt% ammonium borate is added to a phenolic molding material. When the amount of ammonium borate is less than 1wt%, the high- temperature rigidity can not be improved, while when the amount exceeds 19wt%, the injection moldability can not be improved. Examples of the phenolic resins are resol and novolak type phenolic resins, cresol resin, xylenol resin and phenolic resins modified with molasses, lignin, xylene, naphthalene or petroleum arom. hydrocarbon resin. As additives other than the phenolic resin and ammonium borate, conventional hardener, parting agent, colorant, filler, reinforcing agent, etc. can be used as such.

Description

【発明の詳細な説明】 本発明は電子機器、電気機器、自動車用部品、船舶用部
品、厨房用品、雑貨用品等を得るための成形材料に関す
るもので、その目的とするところは射出成形性がよく成
形品の熱時剛性に優れた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 molding material for obtaining electronic equipment, electrical equipment, automobile parts, ship parts, kitchen goods, miscellaneous goods, etc., and its purpose is to have injection moldability. The object of the present invention is to provide a molding material that provides molded products with excellent rigidity when heated.

従来のこの種の成形材料はハイオルソ樹脂を用いている
がこれでは熱時剛性はよいが射出成形性が低下する欠点
があり、又、成形時の材料延びを小さくする方法では熱
時剛性はよくなるが成形圧力が高くなり成形性が低下す
る欠点があった。更にサリチル酸の硬化助剤を添加する
方法では熱時剛性はよくなるが成形性が低下していた。
Conventional molding materials of this type use high-ortho resins, which have good rigidity when hot, but have the disadvantage of poor injection moldability.Additionally, methods that reduce the elongation of the material during molding improve the rigidity when hot. However, there was a drawback that the molding pressure increased and moldability decreased. Furthermore, in the method of adding a curing aid of salicylic acid, the stiffness when heated was improved, but the moldability was lowered.

本発明は上記欠点を解決するもので、ホウ酸アンモニウ
ムを1〜19重量%(以下単に%と記す)含有させるこ
とにょって熱時剛性と射出成形性を併せて向上させるこ
とができたものである。
The present invention solves the above-mentioned drawbacks, and is capable of improving both hot rigidity and injection moldability by containing 1 to 19% by weight (hereinafter simply referred to as %) of ammonium borate. It is.

以下本発明を詳細に説明する。本発明に用いるフェノー
ル樹脂はレゾール型、ノボラック型各れでもよく、又、
クレゾール樹脂、キシレノール樹脂をも含み、更に糖密
、リグニン、キシレン、ナフタリン、石油系芳香族炭化
水素樹脂等による変性フェノール樹脂等をも含むもので
ある。ホウ酸アンモニウムの添加量は1〜19係がよく
1%未満では熱時剛性を向上させることができず、19
%をこえると射出成形性を向上させることができないか
らである。フェノール樹脂、ホウ酸アンモニウム以外の
添加物としては一般に用いられている硬化剤、離型剤、
着色剤、充填剤、補強剤等をそのまま用いることができ
る。これら樹脂、ホウ酸アンモニウム、硬化剤等の配合
物を混合、混練、粉砕、必要に応じて造粒化してフェノ
ール樹脂成形材料を得るものである。
The present invention will be explained in detail below. The phenolic resin used in the present invention may be either a resol type or a novolak type, and
It includes cresol resins and xylenol resins, and also includes phenolic resins modified with molasses, lignin, xylene, naphthalene, petroleum-based aromatic hydrocarbon resins, and the like. The amount of ammonium borate added is preferably 1% to 19%, and if it is less than 1%, the stiffness under heat cannot be improved;
%, injection moldability cannot be improved. Additives other than phenol resin and ammonium borate include commonly used curing agents, mold release agents,
Colorants, fillers, reinforcing agents, etc. can be used as they are. A phenol resin molding material is obtained by mixing, kneading, pulverizing, and, if necessary, granulating a blend of these resins, ammonium borate, a curing agent, and the like.

以下本発明を実施例及び従来例にもとずいて説明する。The present invention will be explained below based on embodiments and conventional examples.

実施例1及び2と従来例 ノボラック型フェノール樹脂を用い第1表の配合表に従
って配合、混合、混練、粉砕してフェノール樹脂成形材
料を得た。
Examples 1 and 2 and conventional novolac type phenolic resins were compounded, mixed, kneaded and pulverized according to the formulation table in Table 1 to obtain phenolic resin molding materials.

実施例1及び2と従来例のフェノール樹脂成形材料を1
00トン型射出成形機でシリンダー後部温度80℃、シ
リンダー前部温度100℃、金型温度160℃でブレー
カーを射出成形した時のシリンダー安定性及びブレーカ
ー成形品の反り(熱時剛性のよいもの程反りは少ない)
は第2表で明白なように本発明のフェノール樹脂成形材
料の射出成形性及び熱時剛性はよく本発明のフェノール
樹脂成形材料の優れていることを確認した。
1 of the phenolic resin molding materials of Examples 1 and 2 and the conventional example
Cylinder stability and warpage of the breaker molded product when injection molding a breaker with a 00 ton injection molding machine at a cylinder rear temperature of 80°C, a cylinder front temperature of 100°C, and a mold temperature of 160°C (the better the rigidity when heated) There is little warping)
As clearly shown in Table 2, it was confirmed that the phenolic resin molding material of the present invention was excellent in injection moldability and thermal rigidity.

Claims (1)

【特許請求の範囲】[Claims] ホウ酸アンモニウムを1〜19 重量%含有したことを
特徴とするフェノール樹脂成形材料。
A phenolic resin molding material containing 1 to 19% by weight of ammonium borate.
JP13551182A 1982-08-02 1982-08-02 Phenolic molding material Pending JPS5924740A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13551182A JPS5924740A (en) 1982-08-02 1982-08-02 Phenolic molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13551182A JPS5924740A (en) 1982-08-02 1982-08-02 Phenolic molding material

Publications (1)

Publication Number Publication Date
JPS5924740A true JPS5924740A (en) 1984-02-08

Family

ID=15153467

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13551182A Pending JPS5924740A (en) 1982-08-02 1982-08-02 Phenolic molding material

Country Status (1)

Country Link
JP (1) JPS5924740A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6142555A (en) * 1984-08-03 1986-03-01 ソシエテ シミック デ シャルボナージュ エス.アー. Novel phenol resin composition
US4584329A (en) * 1984-03-30 1986-04-22 Ruetgerswerke Aktiengesellschaft Hardenable molding masses and their use
JP2008094950A (en) * 2006-10-11 2008-04-24 Starlite Co Ltd Heat-resistant phenolic resin composition excellent in storage stability

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4584329A (en) * 1984-03-30 1986-04-22 Ruetgerswerke Aktiengesellschaft Hardenable molding masses and their use
JPS6142555A (en) * 1984-08-03 1986-03-01 ソシエテ シミック デ シャルボナージュ エス.アー. Novel phenol resin composition
JPH0559146B2 (en) * 1984-08-03 1993-08-30 Charbonnages Ste Chimique
JP2008094950A (en) * 2006-10-11 2008-04-24 Starlite Co Ltd Heat-resistant phenolic resin composition excellent in storage stability

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