JPH0218412A - Flexible epoxy resin composition - Google Patents
Flexible epoxy resin compositionInfo
- Publication number
- JPH0218412A JPH0218412A JP16769388A JP16769388A JPH0218412A JP H0218412 A JPH0218412 A JP H0218412A JP 16769388 A JP16769388 A JP 16769388A JP 16769388 A JP16769388 A JP 16769388A JP H0218412 A JPH0218412 A JP H0218412A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- ether
- resin composition
- weight
- specified
- 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
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 31
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims abstract description 11
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims abstract description 14
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims abstract description 5
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- 125000003118 aryl group Chemical group 0.000 claims abstract description 4
- 238000006482 condensation reaction Methods 0.000 claims abstract description 4
- 239000000539 dimer Substances 0.000 claims abstract description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920000768 polyamine Polymers 0.000 claims abstract description 3
- 150000001412 amines Chemical class 0.000 claims description 10
- 239000004952 Polyamide Substances 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 238000002156 mixing Methods 0.000 abstract description 4
- 229920005989 resin Polymers 0.000 abstract description 3
- 239000011347 resin Substances 0.000 abstract description 3
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 abstract description 2
- 238000005266 casting Methods 0.000 abstract description 2
- -1 alkylene ether Chemical compound 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 4
- 239000011342 resin composition Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 206010011878 Deafness Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000004842 bisphenol F epoxy resin Substances 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- 231100000895 deafness Toxicity 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 208000016354 hearing loss disease Diseases 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000004843 novolac epoxy resin Substances 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Epoxy Resins (AREA)
Abstract
Description
【発明の詳細な説明】
が可撓性に優れ、経時的な硬度変化が少なく、作業性に
優れた注型材に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a casting material that has excellent flexibility, little change in hardness over time, and excellent workability.
従来エポキシ樹脂に可撓性を付与する方法としては、そ
の系に可塑剤を多量に配合する方法が一般的であったが
、多量の可塑剤の配合は電気特性や耐湿性の経時的低下
を招き長期信幀性が劣るという欠点があった。近年では
、可撓性を有するエポキシ系樹脂としてフェノキシ樹脂
等も登場しているが、これらは高分子量であるため粘度
が高く作業性に劣る欠点がある。Conventionally, the common method for imparting flexibility to epoxy resins has been to add large amounts of plasticizers to the system, but adding large amounts of plasticizers can cause electrical properties and moisture resistance to deteriorate over time. The drawback was that long-term reliability was poor. In recent years, phenoxy resins and the like have appeared as flexible epoxy resins, but these have a drawback of high viscosity and poor workability due to their high molecular weight.
(発明が解決しようとする課題〕
本発明は、電気特性、作業性を低下させる事なく、長期
にわたって可撓性を維持する事の出来るエポキシ樹脂組
成物を提供することを目的とするものである。(Problems to be Solved by the Invention) An object of the present invention is to provide an epoxy resin composition that can maintain flexibility over a long period of time without deteriorating electrical properties or workability. .
本発明は、主鎖にアルキレンエーテル結合を含むビスフ
ェノールA型エポキシ樹脂を30〜60重量%含有する
エポキシ樹脂100重量部に対して、脂肪族モノ又はジ
グリシジルエーテル又は芳香族モノグリシジルエーテル
5〜30M量部を配合し、硬化剤としてダイマー酸とジ
アミンとの縮合反応により得られたポリアミドアミンを
配合してなる可撓性エポキシ樹脂組成物である。The present invention applies 5 to 30 M of aliphatic mono- or diglycidyl ether or aromatic monoglycidyl ether to 100 parts by weight of an epoxy resin containing 30 to 60 weight % of bisphenol A type epoxy resin containing an alkylene ether bond in the main chain. This is a flexible epoxy resin composition in which polyamide amine obtained by a condensation reaction of dimer acid and diamine is blended as a curing agent.
本発明においては、エポキシ樹脂の一部として、主鎖に
アルキレンエーテル結合を有するビスフェノールA型エ
ポキシ樹脂(以下、単に「可撓性エポキシ樹脂」という
)を使用する。かかるエポキシ樹脂は通常のエポキシ樹
脂と同じように硬化剤と反応し、可撓性の硬化物を与え
る。市販のものとしては、旭電化■EP−4000等が
ある。In the present invention, a bisphenol A type epoxy resin (hereinafter simply referred to as "flexible epoxy resin") having an alkylene ether bond in the main chain is used as a part of the epoxy resin. Such an epoxy resin reacts with a curing agent in the same way as a normal epoxy resin to give a flexible cured product. Commercially available products include Asahi Denka EP-4000.
他のエポキシ樹脂としては、ビスフェノールA型エポキ
シ樹脂、ビスフェノールF型エポキシ樹脂、ノボラック
型エポキシ樹脂、ポリヒドロキシベンゼン系エポキシ樹
脂、フタル酸やテトラヒドロフタル酸などのガルボン酸
グリシジルエステルなどを例示することができる。これ
らのエポキシ樹脂はエポキシ当量100〜300で液状
のものが、作業性の点から好ましい。Examples of other epoxy resins include bisphenol A epoxy resin, bisphenol F epoxy resin, novolac epoxy resin, polyhydroxybenzene epoxy resin, and galboxylic acid glycidyl esters such as phthalic acid and tetrahydrophthalic acid. . These epoxy resins preferably have an epoxy equivalent of 100 to 300 and are liquid from the viewpoint of workability.
エポキシ樹脂中の可撓性エポキシ樹脂の割合は30〜6
0重量%である。30重量%未満では可成に、脂肪族モ
ノ又はジグリシジルエーテル又は芳香族モノグリシジル
エーテルは反応性希釈剤として配合するものであって、
組成物の低粘度化の他に、硬化物の電気特性を殆んど低
下させずに適度の可撓性を付与する働きがある。具体的
には例えば、ブチルグリシジルエーテル、1.6−へキ
シルグリシジルエーテル、フェニルグリシジルエーテル
などがある。The proportion of flexible epoxy resin in epoxy resin is 30-6
It is 0% by weight. If less than 30% by weight, the aliphatic mono- or diglycidyl ether or the aromatic monoglycidyl ether is blended as a reactive diluent,
In addition to lowering the viscosity of the composition, it has the function of imparting appropriate flexibility to the cured product without substantially reducing its electrical properties. Specific examples include butyl glycidyl ether, 1,6-hexyl glycidyl ether, and phenyl glycidyl ether.
かかる反応希釈剤の配合割合はエポキシ樹脂100重量
部に対して5〜30重量部である。5重量部未満ではそ
の効果が小さく、30重量部を越えると、電気特性に悪
影響を及ぼすようになる。The mixing ratio of such a reaction diluent is 5 to 30 parts by weight per 100 parts by weight of the epoxy resin. If it is less than 5 parts by weight, the effect is small, and if it exceeds 30 parts by weight, it will adversely affect the electrical properties.
本発明においては、硬化剤としてダイマー酸とポリアミ
ンとの縮合反応により得られたポリアミドアミンを配合
する。かかるポリアミドアミンとしてはアミン価300
〜500のものが、作業性、硬化物の可撓性の点で好ま
しく、具体的には、ヘンケル白水社のDSX−178(
アミン値43り尋→等がある。In the present invention, a polyamide amine obtained by a condensation reaction between a dimer acid and a polyamine is blended as a curing agent. Such polyamide amine has an amine value of 300.
~500 is preferable in terms of workability and flexibility of the cured product. Specifically, Henkel Hakusuisha's DSX-178 (
The amine value is 43 fathoms → etc.
配合割合は、ポリアミドアミンの種類、アミン価にもよ
るが、エポキシ樹脂100重量部に対して、80〜15
0重量部が通常好ましい範囲である。80重量部未満で
は可撓性はすぐれているものの、電気特性が低下する傾
向にあり、硬度の経時的変化も生じるようになり、15
0重量部を越えると可撓性が劣る傾向が現われることが
多い。The blending ratio depends on the type of polyamide amine and the amine value, but it is 80 to 15 parts by weight per 100 parts by weight of the epoxy resin.
0 parts by weight is usually the preferred range. If it is less than 80 parts by weight, the flexibility is excellent, but the electrical properties tend to deteriorate and the hardness changes over time.
When the amount exceeds 0 parts by weight, flexibility often tends to be poor.
(実施例)
第1表に示す配合組成にてエポキシ樹脂組成物を調製し
、粘度を測定した。(Example) Epoxy resin compositions were prepared with the formulation shown in Table 1, and the viscosity was measured.
第
表
EP 82B シェル化m エポキシ当1 19
0EP4000 旭電化製 エポキシ当M 32
5エポニツト014 アルコールモノグリシジルエ→
ル(エポキシ当II 215)
この組成物を60°Cで5時間加熱硬化した。その硬化
物について、硬化直後及び80℃にて10日間経過後の
硬度(ショア聾)を80℃にて測定した。Table EP 82B Shelling m Epoxy 1 19
0EP4000 Asahi Denka Epoxy M 32
5 Eponite 014 Alcohol monoglycidyl →
(Epoxy II 215) This composition was cured by heating at 60°C for 5 hours. The hardness (Shore deafness) of the cured product was measured at 80°C immediately after curing and after 10 days at 80°C.
実施例の樹脂組成物は、粘度が低く、得られた硬化物も
ショアD/80℃ 25と可撓性に富んでおり、80°
CtO日間経過後も硬度変化は認められなかった。The resin composition of the example has a low viscosity, and the obtained cured product has a Shore D/80°C of 25 and is highly flexible.
No change in hardness was observed even after CtO days had passed.
比較例1の樹脂組成物は、ショアD/80℃40であり
、柔軟性が不足している。The resin composition of Comparative Example 1 had a Shore D/80°C of 40, and lacked flexibility.
比較例2の樹脂組成物は粘度も低く硬化物もショアD/
80°C10と非常に柔軟性に冨んでいるが、硬化物に
ベタツキがあり、かつ80°C10日間経過後での硬度
変化が大きく長期信較性に欠ける。The resin composition of Comparative Example 2 has a low viscosity and the cured product is Shore D/
Although it is very flexible at 80°C10, the cured product is sticky and the hardness changes significantly after 10 days at 80°C, lacking long-term reliability.
〔発明の効果)
本発明は、可撓性付与のために可撓性エポキシ樹脂とポ
リアミドアミンを使用しているので、硬化物が可撓性に
冨み、かつ経時的な硬度変化の少ないエポキシ樹脂組成
物を得ることができる。[Effects of the Invention] Since the present invention uses a flexible epoxy resin and polyamide amine to impart flexibility, the cured product is highly flexible and the epoxy resin exhibits little change in hardness over time. A resin composition can be obtained.
反応性希釈剤を適度に使用する事により低粘度で作業性
に優れた樹脂を得ることができる。By appropriately using a reactive diluent, a resin with low viscosity and excellent workability can be obtained.
可撓性エポキシ樹脂とポリアミドアミン、それに反応性
希釈剤特に脂肪族グリシジルエーテルの影響により組成
物全体の相溶性がよくなるので反応が均一で、未反応物
が少ない、従って硬化物は電気特性等もすぐれており、
硬度の経時変化も少ない。Due to the influence of the flexible epoxy resin, polyamide amine, and the reactive diluent, especially the aliphatic glycidyl ether, the overall compatibility of the composition is improved, so the reaction is uniform, there are few unreacted substances, and the cured product has good electrical properties. It is excellent;
There is also little change in hardness over time.
Claims (1)
ールA型エポキシ樹脂を30〜60重量含有するエポキ
シ樹脂100重量部に対して、脂肪族モノ又はジグリシ
ジルエーテル又は芳香族モノグリシジルエーテル5〜3
0重量部を配合し、硬化剤としてダイマー酸とポリアミ
ンとの縮合反応により得られたポリアミドアミンを配合
することを特徴とする可撓性エポキシ樹脂組成物。(1) For 100 parts by weight of an epoxy resin containing 30 to 60 parts by weight of bisphenol A type epoxy resin containing an alkylene ether bond in the main chain, 5 to 3 parts by weight of aliphatic mono- or diglycidyl ether or aromatic monoglycidyl ether
1. A flexible epoxy resin composition characterized in that a polyamide amine obtained by a condensation reaction between a dimer acid and a polyamine is blended as a curing agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16769388A JPH0218412A (en) | 1988-07-07 | 1988-07-07 | Flexible epoxy resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16769388A JPH0218412A (en) | 1988-07-07 | 1988-07-07 | Flexible epoxy resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0218412A true JPH0218412A (en) | 1990-01-22 |
Family
ID=15854481
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16769388A Pending JPH0218412A (en) | 1988-07-07 | 1988-07-07 | Flexible epoxy resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0218412A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6160040A (en) * | 1996-12-31 | 2000-12-12 | Shell Oil Company | Water borne capped ester containing epoxy amine adduct curing agents compositions for self-curing epoxy resins at ambient or sub-ambient temperatures |
WO2000079582A1 (en) * | 1999-06-17 | 2000-12-28 | Loctite Corporation | Controllably degradable composition of heteroatom carbocyclic or epoxy resin and curing agent |
US6180727B1 (en) * | 1996-12-31 | 2001-01-30 | Shell Oil Company | Capped ester containing epoxy amine adduct curing agents for curing epoxy resins at ambient or sub-ambient temperatures without external catalysts |
US7012120B2 (en) | 2000-03-31 | 2006-03-14 | Henkel Corporation | Reworkable compositions of oxirane(s) or thirane(s)-containing resin and curing agent |
US8053587B2 (en) | 2000-03-31 | 2011-11-08 | Henkel Corporation | Reworkable thermosetting resin composition |
JP2012201711A (en) * | 2011-03-23 | 2012-10-22 | Kyocera Chemical Corp | Casting epoxy resin composition, and coil part |
-
1988
- 1988-07-07 JP JP16769388A patent/JPH0218412A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6160040A (en) * | 1996-12-31 | 2000-12-12 | Shell Oil Company | Water borne capped ester containing epoxy amine adduct curing agents compositions for self-curing epoxy resins at ambient or sub-ambient temperatures |
US6180727B1 (en) * | 1996-12-31 | 2001-01-30 | Shell Oil Company | Capped ester containing epoxy amine adduct curing agents for curing epoxy resins at ambient or sub-ambient temperatures without external catalysts |
WO2000079582A1 (en) * | 1999-06-17 | 2000-12-28 | Loctite Corporation | Controllably degradable composition of heteroatom carbocyclic or epoxy resin and curing agent |
JP2003502484A (en) * | 1999-06-17 | 2003-01-21 | ヘンケル ロックタイト コーポレイション | Controllable degradable compositions of heteroatom carbocyclic or epoxy resins and curing agents |
JP4718070B2 (en) * | 1999-06-17 | 2011-07-06 | ヘンケル コーポレイション | Underfill sealing and repair method |
US7012120B2 (en) | 2000-03-31 | 2006-03-14 | Henkel Corporation | Reworkable compositions of oxirane(s) or thirane(s)-containing resin and curing agent |
US8053587B2 (en) | 2000-03-31 | 2011-11-08 | Henkel Corporation | Reworkable thermosetting resin composition |
JP2012201711A (en) * | 2011-03-23 | 2012-10-22 | Kyocera Chemical Corp | Casting epoxy resin composition, and coil part |
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