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JPH0542463B2 - - Google Patents
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JPH0542463B2 - - Google Patents

Info

Publication number
JPH0542463B2
JPH0542463B2 JP59080146A JP8014684A JPH0542463B2 JP H0542463 B2 JPH0542463 B2 JP H0542463B2 JP 59080146 A JP59080146 A JP 59080146A JP 8014684 A JP8014684 A JP 8014684A JP H0542463 B2 JPH0542463 B2 JP H0542463B2
Authority
JP
Japan
Prior art keywords
phenolic resin
molding material
resin
present
polyvinyl acetal
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
Application number
JP59080146A
Other languages
Japanese (ja)
Other versions
JPS60223853A (en
Inventor
Tsutomu Nagata
Mitsuo Ito
Masanori Kokubo
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
Original Assignee
Toshiba Chemical Products 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 Toshiba Chemical Products Co Ltd filed Critical Toshiba Chemical Products Co Ltd
Priority to JP8014684A priority Critical patent/JPS60223853A/en
Publication of JPS60223853A publication Critical patent/JPS60223853A/en
Publication of JPH0542463B2 publication Critical patent/JPH0542463B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41JTYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
    • B41J2202/00Embodiments of or processes related to ink-jet or thermal heads
    • B41J2202/01Embodiments of or processes related to ink-jet heads
    • B41J2202/02Air-assisted ejection

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

[発明の技術分野] 本発明は、収縮率の小さい成形品が得られ、か
つ、耐湿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] 従来、フエノール樹脂を主成分とするフエノー
ル樹脂成形材料は、その優れた電気的機械的特性
のため電気・機械部品に幅広く応用されてきた。 また、低コスト、成形性、軽量化等の点から木
粉およびパルプ基材を充填した汎用のフエノール
樹脂成形材料が多く用いられてきた。 しかしながら、かかる汎用フエノール樹脂成形
材料では、木粉、パルプ等を用いているため、成
形時の収縮率、成形品の加熱収縮率、及び成形品
の吸水性が大きく電気・機械的部品に使用した場
合、特に精密部品の用途ではその使用は不可能で
あつた。そのため、低比重のフエノール樹脂成形
材料で、成形品の収縮率を低下する方法として
は、(イ)通常の樹脂/充填剤(木粉、パルプ)比を
小さくする方法、(ロ)木粉、パルプの充填剤のかわ
りに無機質中空体(シラスバルーン、ガラスバル
ーン)を充填する方法等があつた。 (イ)の場合は、低比重、低収縮になるものの材料
の流動性が低下し、成形性が悪化するえうに、耐
湿性(耐吸水性)が低下する欠点がある。また(ロ)
の場合は、通常の無機質充填剤に比べて低比重、
低収縮になるものの、限界があり、それを超える
と成形性および電気特性、機械的強度が著しく低
下する欠点がある。 [発明の目的] 本発明の目的は、上記の欠点に鑑みてなされた
もので成形時および成形品の収縮率を低下させ、
かつ耐湿性に優れた低比重の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、前記の目的を達成すべく鋭意研究を
重ねた結果、ポリビニルアセタール系樹脂を充填
することにより、低収縮、耐湿性、低比重のフエ
ノール樹脂成形材料を得られることを見出したも
のである。 即ち、本発明は、 (A)フエノール樹脂と、(B)一般式 で示されるポリビニルアセタール系樹脂(但し式
中、Rは水素原子又はアルキル基を、nは平均重
合度を表わす)であつて、平均重合度が200〜400
であるものを含有することを特徴とするフエノー
ル樹脂成形材料である。 本発明に用いる(A)フエノール樹脂としては、フ
エノール、クレゾール等のフエノール類、又は糖
蜜、リグニン、キシレン、ナフタレン、石油系芳
香族炭化水素による変性フエノール類に対してホ
ルマリンもしくはパラホルムアルデヒド類を適宜
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縮合物、レゾール型
フエノール樹脂縮合物、又はレゾール型フエノー
ル樹脂縮合物とノボラツク型フエノール樹脂縮合
物等が挙げられ、これらは単独もしくは混合系と
して使用される。 本発明に用いる(B)ポリビニルアセタール系樹脂
としては、ポリビニルホルマール樹脂、ポリビニ
ルアセタール樹脂、ポリビニルブチラール樹脂等
が挙げられ、これらの1種又は2種以上の混合系
として使用される。ポリビニルアセタール系樹脂
の軟化点は、併用するフエノール樹脂と同程度の
もの、例えばポリビニルブチラール樹脂であれば
平均重合度が200〜400程度のものが好ましい。ま
たポリビニルアセタール系樹脂は、フエノール樹
脂との相溶性がよくその樹脂が有する寸法安定
性、耐湿性を成形材料に付与し、低収縮、耐湿性
に優れたものになるものと推察される。 ポリビニルアセタール系樹脂の配合割合は、成
形材料に対して0.1〜30重量%であることが望ま
しい。その配合量が0.1重量%未満では低収縮、
耐湿性に効果がなく、またその配合量が30重量%
を超えると成形性、硬化性が悪くなり実用に適さ
ない。より好ましい配合割合は3〜20重量%の範
囲である。 本発明のフエノール樹脂成形材料は、(A)フエノ
ール樹脂、(B)ポリビニルアセタール樹脂を含有す
ることを特徴とするが、これらの他に必要に応じ
て木粉、パルプ、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
塑剤等を配合することができる。 本発明のフエノール樹脂成形材料は、通常次の
ようにして製造される。まず所定量のフエノール
樹脂、ポリビニルアセタール系樹脂、木粉その他
必要に応じて添加剤を混合し均一に分散させた
後、混練機で加熱混練し、次いで冷却固化させ粉
砕機で適当な大きさに粉砕してフエノール樹脂成
形材料を製造する。 こうして得られたフエノール樹脂成形材料は電
気部品、機械部品として幅広く使用することがで
きる。 [発明の効果] 本発明のフエノール樹脂成形材料は、低比重に
もかかわらず、成形時および成形品の収縮率が低
く、かつ、耐湿性に優れた成形材料であるため、
特に精密成形部品等に使用して好適なものであ
る。 [発明の実施例] 次に、本発明を実施例によつて具体的に説明す
るが、本発明は実施例によつて限定されるもので
はない。以下実施例および比較例で「%」とは
「重量%」を意味するものである。 実施例 1 ノボラツク型フエノール樹脂40%、ポリビニル
ブチラール樹脂5%、木粉35%、ヘキサメチレン
テトラミン8%、その他添加剤12%を常温で混合
し、次いで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製造した。こ
の成形材料を用いて射出成形で170℃に加熱した
金型中に成形硬化させて成形品とした。得られた
成形品について成形収縮率、比重、吸水率をJIS
−K−6911に準じて試験を行つた。 これらの結果を第1表に示した。 比較例 ノボラツク型フエノール樹脂45%、木粉35%、
ヘキサメチレンテトラミン8%、その他添加剤12
%を実施例と同様に操作してフエノール樹脂成形
材料を製造した。次いで実施例と同様にしてこの
成形材料を用いて成形品とし、同様にして成形収
縮率、比重、吸水率を試験した。これらの結果を
第1表に示した。
[Technical Field of the Invention] The present invention relates to a phenolic resin molding material that allows molded products with a small shrinkage rate to be obtained and has excellent moisture resistance. [Technical background of the invention and its problems] Conventionally, phenolic resin molding materials containing phenolic resin as a main component have been widely applied to electrical and mechanical parts due to their excellent electrical and mechanical properties. In addition, general-purpose phenolic resin molding materials filled with wood flour and pulp base materials have been widely used because of their low cost, moldability, and weight reduction. However, since such general-purpose phenolic resin molding materials use wood flour, pulp, etc., the shrinkage rate during molding, the heat shrinkage rate of molded products, and the water absorption of molded products are large, making it difficult to use them for electrical and mechanical parts. In many cases, its use was impossible, especially in applications involving precision parts. Therefore, methods for reducing the shrinkage rate of molded products using low-density phenolic resin molding materials include (a) reducing the usual resin/filler (wood flour, pulp) ratio; (b) wood flour, There was a method of filling inorganic hollow bodies (shirasu balloons, glass balloons) instead of pulp fillers. In the case of (a), although the specific gravity and shrinkage are low, the fluidity of the material is reduced, moldability is deteriorated, and moisture resistance (water absorption resistance) is reduced. Again (b)
In the case of , it has a lower specific gravity than ordinary inorganic fillers,
Although the shrinkage is low, there is a limit beyond which the moldability, electrical properties, and mechanical strength are significantly reduced. [Object of the Invention] The object of the present invention was made in view of the above-mentioned drawbacks, and it is an object of the present invention to reduce the shrinkage rate during molding and of molded products,
The present invention also aims to provide a low specific gravity phenolic resin molding material that has excellent moisture resistance. [Summary of the Invention] As a result of intensive research to achieve the above object, the present invention provides that a phenolic resin molding material with low shrinkage, moisture resistance, and low specific gravity can be obtained by filling with polyvinyl acetal resin. This is what we discovered. That is, the present invention comprises (A) a phenolic resin, and (B) a general formula A polyvinyl acetal resin represented by
This is a phenolic resin molding material characterized by containing the following. The phenolic resin (A) used in the present invention includes phenols such as phenol and cresol, or phenols modified with molasses, lignin, xylene, naphthalene, and petroleum aromatic hydrocarbons, and formalin or paraformaldehyde as appropriate. Novolak-type phenolic resin condensates, resol-type phenolic resin condensates, or resol-type phenolic resin condensates and novolak-type phenolic resin condensates obtained by blending them in a molar ratio and reacting them under a catalyst, etc. Used alone or in combination. Examples of the polyvinyl acetal resin (B) used in the present invention include polyvinyl formal resin, polyvinyl acetal resin, polyvinyl butyral resin, etc., and these resins may be used alone or as a mixture of two or more thereof. The softening point of the polyvinyl acetal resin is preferably similar to that of the phenol resin used in combination, for example, in the case of polyvinyl butyral resin, the average degree of polymerization is preferably about 200 to 400. It is also assumed that polyvinyl acetal resin has good compatibility with phenolic resin and imparts the dimensional stability and moisture resistance of the resin to the molding material, resulting in low shrinkage and excellent moisture resistance. The blending ratio of the polyvinyl acetal resin is preferably 0.1 to 30% by weight based on the molding material. If the amount is less than 0.1% by weight, the shrinkage will be low.
It has no effect on moisture resistance, and its content is 30% by weight.
If it exceeds this value, the moldability and curing properties deteriorate, making it unsuitable for practical use. A more preferable blending ratio is in the range of 3 to 20% by weight. The phenolic resin molding material of the present invention is characterized by containing (A) a phenolic resin and (B) a polyvinyl acetal resin, but in addition to these, wood flour, pulp, a hardening agent, a coloring agent, curing accelerator,
Flame retardants, mold release agents, lubricants, coupling agents, plasticizers, etc. can be added. The phenolic resin molding material of the present invention is usually produced as follows. First, a predetermined amount of phenolic resin, polyvinyl acetal resin, wood flour, and other additives as necessary are mixed and dispersed uniformly, then heated and kneaded in a kneader, then cooled and solidified, and then crushed into appropriate sizes by a pulverizer. Pulverize to produce phenolic resin molding material. The phenolic resin molding material thus obtained can be widely used as electrical parts and mechanical parts. [Effects of the Invention] The phenolic resin molding material of the present invention has a low shrinkage rate during molding and molded products despite its low specific gravity, and is a molding material with excellent moisture resistance.
It is particularly suitable for use in precision molded parts. [Examples of the Invention] Next, the present invention will be specifically explained using Examples, but the present invention is not limited by the Examples. In the following Examples and Comparative Examples, "%" means "% by weight". Example 1 40% novolac type phenolic resin, 5% polyvinyl butyral resin, 35% wood flour, 8% hexamethylenetetramine, and 12% other additives were mixed at room temperature, then kneaded at 90°C to 110°C and cooled. rear,
It was pulverized to produce a phenolic resin molding material. This molding material was injection molded into a mold heated to 170°C and cured to form a molded product. The molding shrinkage rate, specific gravity, and water absorption rate of the obtained molded product are determined according to JIS standards.
-Test was conducted according to K-6911. These results are shown in Table 1. Comparative example Novolac type phenolic resin 45%, wood flour 35%,
Hexamethylenetetramine 8%, other additives 12
% was operated in the same manner as in the examples to produce a phenolic resin molding material. Next, a molded article was made using this molding material in the same manner as in the example, and molding shrinkage, specific gravity, and water absorption were tested in the same manner. These results are shown in Table 1.

【表】 第1表からも明らかなように、本発明のフエノ
ール樹脂成形材料が成形収縮率、吸水率に優れて
いることがわかる。
[Table] As is clear from Table 1, it can be seen that the phenolic resin molding material of the present invention has excellent molding shrinkage and water absorption.

Claims (1)

【特許請求の範囲】 1 (A)フエノール樹脂と、(B)一般式 で示されるポリビニルアセタール系樹脂(但し式
中、Rは水素原子又はアルキル基を、nは平均重
合度を表わす)であつて、平均重合度が200〜400
であるものを含有することを特徴とするフエノー
ル樹脂成形材料。 2 ポリビニルアセタール系樹脂が、成形材料に
対して0.1〜30重量%含有されている特許請求の
範囲第1項記載のフエノール樹脂成形材料。
[Claims] 1 (A) phenolic resin, (B) general formula A polyvinyl acetal resin represented by
A phenolic resin molding material characterized by containing the following. 2. The phenolic resin molding material according to claim 1, wherein the polyvinyl acetal resin is contained in an amount of 0.1 to 30% by weight based on the molding material.
JP8014684A 1984-04-23 1984-04-23 Phenolic resin molding material Granted JPS60223853A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8014684A JPS60223853A (en) 1984-04-23 1984-04-23 Phenolic resin molding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8014684A JPS60223853A (en) 1984-04-23 1984-04-23 Phenolic resin molding material

Publications (2)

Publication Number Publication Date
JPS60223853A JPS60223853A (en) 1985-11-08
JPH0542463B2 true JPH0542463B2 (en) 1993-06-28

Family

ID=13710133

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8014684A Granted JPS60223853A (en) 1984-04-23 1984-04-23 Phenolic resin molding material

Country Status (1)

Country Link
JP (1) JPS60223853A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5527342A (en) * 1978-08-16 1980-02-27 Sekisui Chem Co Ltd Adhesive composition

Also Published As

Publication number Publication date
JPS60223853A (en) 1985-11-08

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