JPH11106603A - Phenolic resin composition - Google Patents
Phenolic resin compositionInfo
- Publication number
- JPH11106603A JPH11106603A JP27675897A JP27675897A JPH11106603A JP H11106603 A JPH11106603 A JP H11106603A JP 27675897 A JP27675897 A JP 27675897A JP 27675897 A JP27675897 A JP 27675897A JP H11106603 A JPH11106603 A JP H11106603A
- Authority
- JP
- Japan
- Prior art keywords
- polyamide
- phenolic resin
- resin composition
- melting point
- melting
- 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
- 239000005011 phenolic resin Substances 0.000 title claims abstract description 23
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 239000000203 mixture Substances 0.000 title claims abstract description 17
- 229920001568 phenolic resin Polymers 0.000 title claims abstract description 17
- 239000004952 Polyamide Substances 0.000 claims abstract description 25
- 229920002647 polyamide Polymers 0.000 claims abstract description 25
- 238000002844 melting Methods 0.000 claims abstract description 11
- 230000008018 melting Effects 0.000 claims abstract description 11
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 6
- 239000000194 fatty acid Substances 0.000 claims abstract description 6
- 229930195729 fatty acid Natural products 0.000 claims abstract description 6
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 4
- 150000004985 diamines Chemical group 0.000 claims abstract description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 claims abstract description 4
- 238000006068 polycondensation reaction Methods 0.000 claims abstract description 4
- 125000003368 amide group Chemical group 0.000 claims abstract description 3
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 229920003986 novolac Polymers 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 238000001721 transfer moulding Methods 0.000 description 3
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 239000003365 glass fiber 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
- 239000007788 liquid Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は耐熱性、強靱性、加
工性に優れるフェノール系樹脂組成物に関するものであ
る。TECHNICAL FIELD The present invention relates to a phenolic resin composition having excellent heat resistance, toughness and processability.
【0002】[0002]
【従来の技術】従来のフェノール樹脂は比較的脆いとい
う欠点を有している、これを改良する方法として各種エ
ラストマー、エンプラなどとのブレンドが行われてい
る。このなかでも特にポリアミドとフェノール樹脂のブ
レンドは樹脂同士の相溶性が良いため、良好な強靱性を
示す。しかし、ポリアミドの融点が高いためブレンドし
て得られる樹脂は軟化点が高くなり、フェノール樹脂の
硬化温度と軟化点の差が小さくなり、加工する際に流動
性が悪くなったり、ポットライフが短くなってしまう欠
点があった。2. Description of the Related Art A conventional phenol resin has a disadvantage that it is relatively brittle. As a method for improving this, a blend with various elastomers, engineering plastics, and the like has been performed. Among them, a blend of a polyamide and a phenolic resin shows good toughness because the compatibility between the resins is good. However, since the melting point of polyamide is high, the resin obtained by blending has a high softening point, the difference between the curing temperature and the softening point of the phenolic resin is small, and the fluidity becomes poor during processing, and the pot life is short. There was a disadvantage that it became.
【0003】[0003]
【発明が解決しようとする課題】本発明は、強靱性に優
れ、かつ加工性、耐熱性に優れるフェノール樹脂組成物
を得るため鋭意検討したものである。DISCLOSURE OF THE INVENTION The present invention has been intensively studied in order to obtain a phenolic resin composition which is excellent in toughness, workability and heat resistance.
【0004】[0004]
【課題を解決するための手段】本発明は、フェノール樹
脂と、重合脂肪酸のカルボキシル残基および/またはC
2〜C21の各種ジカルボン酸とジアミンの重縮合で得
られるポリアミドを混合、溶融して得られるフェノール
樹脂とポリアミドの重量比が100:5〜5:100で
あることを特徴とするフェノール樹脂組成物であり、ポ
リアミドが融点80〜130℃のポリアミドである前記
のフェノール樹脂組成物であり、また、ポリアミドの架
橋剤として、ポリアミドのアミド基の当量に対してビス
エポキシを0.1〜1の割合で添加する特徴とするフェ
ノール樹脂組成物である。SUMMARY OF THE INVENTION The present invention provides a phenolic resin, a carboxyl residue and / or C
A phenolic resin composition characterized in that the weight ratio of the phenolic resin to the polyamide obtained by mixing and melting a polyamide obtained by polycondensation of various C2 to C21 dicarboxylic acids and diamines is 100: 5 to 5: 100. Wherein the polyamide is a phenolic resin composition having a melting point of 80 to 130 ° C., and as a cross-linking agent for the polyamide, a ratio of bisepoxy of 0.1 to 1 relative to the equivalent weight of the amide group of the polyamide. A phenolic resin composition characterized by being added in
【0005】[0005]
【発明の実施の形態】本発明は、ブレンドするポリマー
として比較的低融点の脂肪酸系ポリアミドを用いること
により加工性を、更にポリアミドを部分架橋させること
により耐熱性を損なうことなくフェノール樹脂に強靱性
を付与する事ができる。BEST MODE FOR CARRYING OUT THE INVENTION The present invention provides a phenolic resin having a high toughness without impairing the processability by using a fatty acid polyamide having a relatively low melting point as a polymer to be blended, and further, by impairing the heat resistance by partially crosslinking the polyamide. Can be given.
【0006】本発明で用いるフェノール樹脂は、一般に
使われている物なら用いることができる。ノボラック、
レゾールどちらでも良く、化学的に変成された構造を有
していても良い。As the phenol resin used in the present invention, any commonly used phenol resin can be used. Novolak,
Either resol may be used, and it may have a chemically modified structure.
【0007】本発明で用いるポリアミドは重合脂肪酸の
カルボキシル残基および/またはC2〜C21の各種ジ
カルボン酸とジアミンの重縮合で得られるポリアミドで
融点が好ましくは80〜130℃、より好ましくは90
〜110℃である。The polyamide used in the present invention is a polyamide obtained by polycondensation of a carboxyl residue of a polymerized fatty acid and / or various dicarboxylic acids of C2 to C21 with a diamine, and preferably has a melting point of 80 to 130 ° C., more preferably 90 to 130 ° C.
110110 ° C.
【0008】本発明においてポリアミドの部分架橋にも
ちいるビスエポキシは一般に使われるものはどれも使用
出来るが、液状のものが好ましくあらかじめポリアミド
と溶融混合しておくことが望ましい。In the present invention, any commonly used bisepoxy used for partial cross-linking of polyamide can be used, but liquid epoxy is preferred, and it is desirable to melt-mix it with polyamide in advance.
【0009】[0009]
(実施例1)フェノールノボラック(軟化点97℃)1
40gと融点100℃の脂肪酸系ポリアミド(アミド当
量180)60gにジグリシジルビスフェノールA(エ
ポキシ当量180)12gを混練機で120℃で溶融混
合し樹脂A(軟化点98℃)を得た。A100gにヘキ
サミン15g、酸化マグネシウム5g、ガラス繊維20
0gを加え、ロール混練後粉砕して、ペレットを得た。
175℃、3分間トランスファー成型機にてテストピー
スを作成した。結果を表1に示す。(Example 1) Phenol novolak (softening point 97 ° C) 1
12 g of diglycidylbisphenol A (epoxy equivalent: 180) was melt-mixed at 120 ° C. with 40 g and 60 g of a fatty acid-based polyamide (amide equivalent: 180) having a melting point of 100 ° C. at 120 ° C. to obtain a resin A (softening point: 98 ° C.). A100g, hexamine 15g, magnesium oxide 5g, glass fiber 20
After adding 0 g, the mixture was kneaded with a roll and then pulverized to obtain a pellet.
Test pieces were prepared at 175 ° C. for 3 minutes using a transfer molding machine. Table 1 shows the results.
【0010】(実施例2)フェノールノボラック(軟化
点97℃)100gと融点110℃の脂肪酸系ポリアミ
ド(アミド当量180)100gにジグリシジルビスフ
ェノールA(エポキシ当量180)40gを混練機で1
20℃で溶融混合し樹脂B(軟化点105℃)を得た。
実施例1の樹脂Aの代わりに樹脂Bを用い同様にしてペ
レットを得た。175℃、3分間トランスファー成型機
にてテストピースを作成した。結果を表1に示す。Example 2 100 g of phenol novolak (softening point: 97 ° C.) and 100 g of a fatty acid-based polyamide (amide equivalent: 180) having a melting point of 110 ° C. were mixed with 40 g of diglycidylbisphenol A (epoxy equivalent: 180) by a kneader.
The mixture was melted and mixed at 20 ° C. to obtain resin B (softening point: 105 ° C.).
Pellets were obtained in the same manner as in Example 1 except that resin B was used instead of resin A. Test pieces were prepared at 175 ° C. for 3 minutes using a transfer molding machine. Table 1 shows the results.
【0011】(比較例1)実施例1の樹脂Aの代わりに
フェノールノボラック(軟化点95℃)を用い同様にし
てペレットを得た。175℃、3分間トランスファー成
型機にてテストピースを作成した。結果を表1に示す。Comparative Example 1 Pellets were obtained in the same manner as in Example 1, except that phenol novolak (softening point: 95 ° C.) was used instead of resin A. Test pieces were prepared at 175 ° C. for 3 minutes using a transfer molding machine. Table 1 shows the results.
【0012】[0012]
【表1】 [Table 1]
【0013】[0013]
【発明の効果】本発明のフェノール樹脂組成物は、強靱
性に優れ、かつ加工性、耐熱性に優れている。The phenolic resin composition of the present invention is excellent in toughness, workability and heat resistance.
Claims (3)
キシル残基および/またはC2〜C21の各種ジカルボ
ン酸とジアミンの重縮合で得られるポリアミドを混合、
溶融して得られるフェノール樹脂とポリアミドの重量比
が100:5〜5:100であることを特徴とするフェ
ノール樹脂組成物。1. A phenolic resin mixed with a carboxyl residue of a polymerized fatty acid and / or a polyamide obtained by polycondensation of diamines with various C2 to C21 dicarboxylic acids,
A phenol resin composition, wherein the weight ratio of the phenol resin and the polyamide obtained by melting is from 100: 5 to 5: 100.
アミドである請求項1記載のフェノール樹脂組成物。2. The phenolic resin composition according to claim 1, wherein the polyamide has a melting point of 80 to 130 ° C.
ポリアミドのアミド基の当量に対してビスエポキシを
0.1〜1の割合で添加する特徴とするフェノール樹脂
組成物。3. The crosslinking agent for the polyamide according to claim 2,
A phenol resin composition, characterized in that bisepoxy is added at a ratio of 0.1 to 1 with respect to the equivalent of the amide group of the polyamide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27675897A JPH11106603A (en) | 1997-10-09 | 1997-10-09 | Phenolic resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27675897A JPH11106603A (en) | 1997-10-09 | 1997-10-09 | Phenolic resin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11106603A true JPH11106603A (en) | 1999-04-20 |
Family
ID=17573947
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27675897A Pending JPH11106603A (en) | 1997-10-09 | 1997-10-09 | Phenolic resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11106603A (en) |
-
1997
- 1997-10-09 JP JP27675897A patent/JPH11106603A/en active Pending
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