JPS6366242A - Air-permeating material - Google Patents

Air-permeating material

Info

Publication number
JPS6366242A
JPS6366242A JP20919986A JP20919986A JPS6366242A JP S6366242 A JPS6366242 A JP S6366242A JP 20919986 A JP20919986 A JP 20919986A JP 20919986 A JP20919986 A JP 20919986A JP S6366242 A JPS6366242 A JP S6366242A
Authority
JP
Japan
Prior art keywords
polyepoxide
curing
solid particles
bisphenol
diglycidyl ether
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
JP20919986A
Other languages
Japanese (ja)
Inventor
Koichi Kakefuda
掛札 紘一
Toshitatsu Shimoide
下出 敏達
Teruo Tejima
照雄 手島
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.)
Resonac Corp
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP20919986A priority Critical patent/JPS6366242A/en
Publication of JPS6366242A publication Critical patent/JPS6366242A/en
Pending legal-status Critical Current

Links

Landscapes

  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

PURPOSE:To obtain an air-permeable material having improved flexural modulus, flexural strain at break and crack resistance and suitable for filter, material for suction-holding, etc., by compounding solid particles having specific particle diameter with a polyepoxide and its hardener. CONSTITUTION:The objective material can be produced by compounding (A) solid particles having a void ratio of >=40vol% and an average particle diameter of <=100mum (e.g. aluminum powder) with (B) a polyepoxide forming a hard resin by curing (e.g. glycidyl compound of bisphenol A, etc.) and its hardener (e.g. diaminodiphenylmethane) and (C) an oil-modified bisphenol A diglycidyl ether polyepoxide. The weight ratio of the polyepoxide of the component B to the component C is 95:5-70:30 and the volume ratio of the component A to the sum of the components B and C is 90:10-70:30.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はフィルターや吸引保持用材料あるいは真空成形
用型材料として有用な強度のすぐtた通気性部材に関す
る。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a high-strength breathable member useful as a filter, a suction holding material, or a mold material for vacuum forming.

(従来の技術) 従米通気性部拐としては、セラミック糸パウダーにバイ
ングーとしてエテル7リケートなどを加え焼結したもの
や、ステルパウダーをエポキシ樹脂でコーティングし成
形後加熱硬化しkものなどが知られている。
(Prior technology) Known examples of air-permeable fabrics include those made by adding and sintering ether 7-lysate as bindu to ceramic thread powder, and those made by coating stell powder with epoxy resin and curing it by heating after molding. ing.

しかし前者に於いては、焼結に高い温#全必要とする事
などの他寸法精度に問題が残されている。又後者におい
ては、機械的強度特に耐クラツク性の向上が望tnてい
る。
However, in the former case, other problems remain in dimensional accuracy, such as the need for high temperatures for sintering. In the latter case, it is desired to improve mechanical strength, particularly crack resistance.

(発明が解決しようとする間旬点) 本発明は、平均粒子径が100μm以下の固体粒子とポ
リエポキシド及びその硬化剤とを含んでなる通気性部材
に於いてその機械的強度特に曲げ弾性率及び破断曲げ撓
みを改良して耐りラック性を向上させること全目的とす
る。
(Intermediate Point to be Solved by the Invention) The present invention provides an air-permeable member comprising solid particles having an average particle diameter of 100 μm or less, polyepoxide, and a curing agent thereof. The overall purpose is to improve rack resistance by improving bending deflection at break.

(問題点を解決するための手段) 下記tA) 、 IB)及びtQ ’(r必須成分とし
て配合し硬化してなる通気性部材 (N 平均粒子径が100μm以下の固体粒子(B) 
 6e化後硬質樹脂を形成するポリエポキシド及びその
硬化剤 FC)  油脂変性ビスフェノールAジグリフジルエー
テル系ポリエポキシド に関するもので、従来の硬質ポリエポキンド/硬化剤系
に油脂変性ビスフェノ−3Aジグリフジル工−テル系ポ
リエポキシド全配合した事全特徴とする。
(Means for solving the problem) The following tA), IB) and tQ' (r) A breathable member (N) formed by blending and curing as essential components Solid particles (B) with an average particle diameter of 100 μm or less
Polyepoxide that forms a hard resin after 6e conversion and its curing agent FC) This relates to oil-modified bisphenol A diglyfusyl ether polyepoxide, which is a complete blend of oil-modified bisphenol A diglyfusyl ether polyepoxide in a conventional hard polyepkind/curing agent system. All the features are the same.

本来油脂変性ビスフェノールAジグリシジルエーテル系
ポリエポキシドなどの内部0]酸化ポリエポキシドは、
そt自身の硬化物は軟かいものであり、ビスフェノール
Aジグリシジルエーテルなどの硬質ポリエポキシドに配
合した場合、その硬化物を柔軟にする性質を有するもの
であるが、通気性部材を製造する処方に於いては逆に曲
げ弾性率が向上して、耐クラツク性が改良さnること金
兄い出し本発明を得た。
Internally oxidized polyepoxides such as oil-modified bisphenol A diglycidyl ether polyepoxides are
The cured product itself is soft, and when blended with hard polyepoxides such as bisphenol A diglycidyl ether, it has the property of making the cured product flexible. On the contrary, the bending modulus of elasticity is improved, and the crack resistance is improved.

本発明で使井さnる平均粒子径が100μm以下の固体
粒子としてはアルミニウムやニッケル、鉄などの金属粒
子の他ガラス、ソリ力、シリコーンカーバイトなどの無
機系粒子、硬化エポキシ樹脂などのプラスチック粒子な
どから選は2″した1柚以上の粒子が使用さγしる。使
用される固体粒子はその空隙率が、通気性を盛保する上
で重要であり、固体粒子を一定量人nた容器を上下動さ
せ容積が一定になった所で求めた空隙率(パウダー空隙
率)が40容績%以上であることが望ましい。
In the present invention, the solid particles with an average particle diameter of 100 μm or less include metal particles such as aluminum, nickel, and iron, as well as glass, warping particles, inorganic particles such as silicone carbide, and plastics such as hardened epoxy resin. Particles with a size of 2" or more are used.The porosity of the solid particles used is important for maintaining air permeability, and a certain amount of solid particles are used. It is desirable that the porosity (powder porosity) determined by moving the container up and down and when the volume becomes constant is 40% by volume or more.

硬化後硬質樹脂を形成するポリエポキシド及びその硬化
剤は、ポリエポキシドとしてはビスフェノールA、Fお
よびSのグリシジル化合物、フェノールノボラックやク
レゾールノボラツタなどのグリシジル化合物、芳香族ア
ミンのグリシジル化合物および環状脂肪族エポキシ樹脂
などから選は扛、%にビスフェノールAのグリシジル化
合物が好ましい。硬化剤としてはジアミノジフェニルメ
タンやジアミノジフェニルスルホンなどの芳香族ジアミ
ン、ヘキサヒドロ無水フタxfliやエンドメチレンテ
トラヒドロ無水2タル酸などの酸無水物あるい(エフヱ
ノールノボラック樹脂などから選ばn又硬化促進剤とし
てイミダゾール化合物や三フッ化ホウ素のアミン錯体を
併用する事が出来る。
The polyepoxide and its curing agent that form a hard resin after curing include glycidyl compounds of bisphenol A, F, and S, glycidyl compounds such as phenol novolac and cresol novolac, glycidyl compounds of aromatic amines, and cycloaliphatic epoxy resins. Glycidyl compounds with bisphenol A in % are preferred. As a curing agent, it is selected from aromatic diamines such as diaminodiphenylmethane and diaminodiphenylsulfone, acid anhydrides such as hexahydrofanhydride xfli and endomethylenetetrahydroditalic anhydride (ewenol novolak resin, etc.), and as a curing accelerator. An imidazole compound or an amine complex of boron trifluoride can be used in combination.

油脂変性ビスフェノールAジグリシジルエーテル系ポリ
エポキシドは分子中に−OH基を有する燃油脂にビスフ
ェノールAジグリシジルエーテル全付加して得られる液
状の内f15可塑化ボリエボキ7ドである。
Oil-modified bisphenol A diglycidyl ether-based polyepoxide is a liquid F15 plasticized polyepoxide obtained by total addition of bisphenol A diglycidyl ether to fuel oil having an -OH group in the molecule.

硬化後硬質樹脂を形成するポリエポキシドと油脂変性ビ
スフェノールAジグリシジルエーテル系ポリエポキシド
の配合比率は重量比で95=5へ70:30で1更用さ
れる。油脂変性ビスフェノ−3Aジグリクジルエーテル
系ポリエポキシドの使用量が70 : 30より多(な
ると曲げ弾性率の向上効果が小さくなるばかりでなく、
耐熱変形性が低下し実用性ケ損なう恐γLがある。
After curing, the blending ratio of the polyepoxide to form the hard resin and the oil-modified bisphenol A diglycidyl ether polyepoxide is changed to 95=5 by weight to 70:30. If the amount of fat-modified bispheno-3A diglycyl ether polyepoxide used is more than 70:30 (if this is the case, not only will the effect of improving the flexural modulus become smaller;
There is a risk that heat deformation resistance will be reduced and practicality will be impaired.

又平均粒子径が100μm以下の固体粒子と硬化後@質
榴脂會形成するポリエポキシド、その硬化剤及び油脂変
性ビスフェノールAジグリシジルエーテル系ポリエポキ
シドの台計賃との配合比率は容積比で90:10〜7[
1:6[1で使用さ扛る。
In addition, the blending ratio of solid particles with an average particle size of 100 μm or less, the polyepoxide that forms a solid resin association after curing, its curing agent, and the oil-modified bisphenol A diglycidyl ether-based polyepoxide is 90:10 by volume. ~7[
1:6[Used in 1.

(作用) 硬化して硬質樹脂を形成するポリエポキシドに油脂変性
ビスフェノールAジグリシジルエーテル系ポリエポキシ
ドを組付せる事により硬化エポキシ樹脂の脆さが改良さ
れ、(AJ平均粒子径が100μm以下の固体粒子、(
B)硬化して硬質樹脂を形成するポリエポキシド及びそ
の硬化剤、tel 油脂変性ビスフェノールAジグリシ
ジルエーテル系ポリエポキシドを必須成分として配合し
硬化することにより曲げ弾性率の同上の他破断曲げ撓み
も向上して耐クラツク性に丁ぐれた通気性部材の製造が
可能となった。
(Function) The brittleness of the cured epoxy resin is improved by assembling the oil-modified bisphenol A diglycidyl ether polyepoxide to the polyepoxide that is cured to form a hard resin. (
B) Polyepoxide that hardens to form a hard resin and its curing agent, oil-modified bisphenol A diglycidyl ether polyepoxide is blended as an essential component and cured to improve the flexural modulus as well as the bending deflection at break. It has become possible to manufacture breathable members with excellent crack resistance.

(実施例) 〔実施例1〕 樹脂組成物(A+を下記比率で計1混合調整した。(Example) [Example 1] A total of one resin composition (A+) was mixed and adjusted at the following ratio.

硬化後硬質樹脂を形成するポリエポキシド(エピコート
828;油化シェルエボキク■製 ビスフェノールAジ
グリシジルエーテル)          21.2W
t部同上硬化剤 (HT972;油化ゾエルエボキ/■製芳香族ジアミン
)       5.9#油脂変性ビスフエノールAジ
グリシジルエーテル系ポリエポキシド     18 
1(エボミックR−151;三井石油化学■製)溶剤(
メチレンクロライド)31.5F次に、アルミニウム粒
子(平均粒子径44μm以下、ハウダー空隙率50%)
140Wt部、ニッケル粒子(平均粒子径44μ以下、
ハウダー空隙率54%)19OWt部全混合機に入tて
混合し、その中Vc佃脂組成物(へ會混合しながら少し
づつ重加する。光分混合した後、綿布の上に広げて空気
全欧きつけながら約6時間風乾する。得られたエポキシ
樹脂被援固体枚千をもみほぐし、成形型に軒くつきなか
ら光てんする。
Polyepoxide that forms a hard resin after curing (Epikoat 828; Bisphenol A diglycidyl ether manufactured by Yuka Shell Ebokiku ■) 21.2W
t part Same as above curing agent (HT972; aromatic diamine manufactured by Yuka Zoel Ebuki/■) 5.9#Oil-fat modified bisphenol A diglycidyl ether polyepoxide 18
1 (Evomic R-151; manufactured by Mitsui Petrochemicals) Solvent (
Methylene chloride) 31.5F Next, aluminum particles (average particle size 44 μm or less, Howder porosity 50%)
140Wt part, nickel particles (average particle size 44μ or less,
Howder porosity 54%) 19OWt part is mixed in a mixing machine, and the Vc tsukuda composition (add it little by little while mixing).After light mixing, spread it on a cotton cloth and air it. Air-dry for about 6 hours while soaking.The obtained epoxy resin-covered solid sheet is loosened and heated from the bottom to the mold.

次に50℃/12時間+120℃/1時間+150℃/
1時間+iao℃/1時間の条件で硬化させ厚さ約8m
mの成形体を得た。
Next, 50℃/12 hours + 120℃/1 hour + 150℃/
Cured under conditions of 1 hour + iao℃/1 hour to a thickness of approximately 8 m.
A molded body of m was obtained.

得られた成形体についてJIS−に69+1に準じて曲
げ特性を評価した。試験条件は曲げ速匪4 mm 7分
、支点間距離106.61111Tlで行った。
The bending properties of the obtained molded body were evaluated according to JIS-69+1. The test conditions were a bending speed of 4 mm, 7 minutes, and a distance between fulcrums of 106.61111 Tl.

試験結果は表−1に示した。The test results are shown in Table-1.

〔実施例2〕 エピコート828を18.7Wt都、エポミックR−1
51を6.3Wt部、HT972を5.5Wt部とした
以外は実施例IK準じた。
[Example 2] Epicort 828 was 18.7 Wt, Epomic R-1
Example IK was followed except that 6.3 Wt parts of 51 and 5.5 Wt parts of HT972 were used.

〔比較例1〕 エピコート828を25、OWt部、エボミックR−1
51をOWし部HT972全6.5Wt部とした以外は
実施例1に準じた。
[Comparative Example 1] 25% of Epicoat 828, OWt part, Evomic R-1
The procedure of Example 1 was followed except that 51 was OWed and the total part of HT972 was 6.5 Wt.

〔比較例2〕 エピコート828、エボiツクR−151の代りに、木
端カルボキシル基液状ポリ(ブタジェン−アクリロニト
リル)(CTBN)変性ビスフェノールA・ングリシジ
ルエーテル系ポリエポキシド(エピクロンTSR−96
0;(BTCN含有量15%)大日本インキ化学工菓■
衾)全25Wt部、HT972を4.9Wt部とした以
外に実施例1Vc準じた。
[Comparative Example 2] Instead of Epicort 828 and Evoic R-151, wood end carboxyl-based liquid poly(butadiene-acrylonitrile) (CTBN) modified bisphenol A/nglycidyl ether polyepoxide (Epicron TSR-96
0; (BTCN content 15%) Dainippon Ink Kagaku Koka ■
衾) Example 1Vc was followed except that the total amount was 25 Wt parts and HT972 was 4.9 Wt parts.

表−1 (発明の効果) 表−1にfとめた結果に示された如く、油脂変性−ビス
フェノールA・ジグリフジルエーテル系ポリエボキ7ド
を配付する率で曲げ弾性率及び破断曲げ撓みが同上し、
従って成形体に対する曲げ応力に対しクランクが発生し
にくNなった。
Table 1 (Effects of the invention) As shown in the results shown in Table 1, the flexural modulus and bending deflection at break were the same as above at the distribution rate of oil-modified bisphenol A diglyphyl ether polyepoxy 7. ,
Therefore, cranking was less likely to occur due to bending stress on the molded body.

Claims (1)

【特許請求の範囲】 1、下記(A)、(B)および(C)を必須成分として
配合し硬化してなる通気性部材。 (A)平均粒子径が100μm以下の固体粒子 (B)硬化後硬質樹脂を形成するポリエポキシド及びそ
の硬化剤 (C)油脂変性ビスフェノールAジグリシジルエーテル
系ポリエポキシド 2、平均粒子径が100μm以下の固体粒子がアルミニ
ウムパウダーを主成分とし、その空隙率が40容積%以
上である特許請求の範囲第1項記載の通気性部材。 3、硬化後硬質樹脂を形成するポリエポキシドがビスフ
ェノールAジグリシジルエーテル系ポリエポキシドであ
り、その硬化剤が芳香族ジアミンを主成分とするもので
ある特許請求の範囲第1項記載の通気性部材。
[Scope of Claims] 1. A breathable member formed by blending and curing the following (A), (B) and (C) as essential components. (A) Solid particles with an average particle size of 100 μm or less (B) Polyepoxide and its curing agent that form a hard resin after curing (C) Oil-modified bisphenol A diglycidyl ether polyepoxide 2, solid particles with an average particle size of 100 μm or less The breathable member according to claim 1, wherein the air-permeable member has aluminum powder as a main component and has a porosity of 40% by volume or more. 3. The breathable member according to claim 1, wherein the polyepoxide that forms the hard resin after curing is a bisphenol A diglycidyl ether polyepoxide, and the curing agent is one containing aromatic diamine as a main component.
JP20919986A 1986-09-05 1986-09-05 Air-permeating material Pending JPS6366242A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20919986A JPS6366242A (en) 1986-09-05 1986-09-05 Air-permeating material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20919986A JPS6366242A (en) 1986-09-05 1986-09-05 Air-permeating material

Publications (1)

Publication Number Publication Date
JPS6366242A true JPS6366242A (en) 1988-03-24

Family

ID=16568992

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20919986A Pending JPS6366242A (en) 1986-09-05 1986-09-05 Air-permeating material

Country Status (1)

Country Link
JP (1) JPS6366242A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999016603A1 (en) * 1997-09-30 1999-04-08 Ngk Insulators, Ltd. Porous membrane comprising ceramic and containing plastic as binder

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999016603A1 (en) * 1997-09-30 1999-04-08 Ngk Insulators, Ltd. Porous membrane comprising ceramic and containing plastic as binder

Similar Documents

Publication Publication Date Title
US4798761A (en) Epoxy resin compositions for use in low temperature curing applications
EP0127198B1 (en) Preimpregnated reinforcements and high strength composites therefrom
JP5403184B1 (en) Fiber reinforced composite material
JP4821163B2 (en) Epoxy resin composition for fiber reinforced composite materials
WO2011163282A2 (en) Curable epoxy resin compositions and composites made therefrom
JP2007126637A (en) Resin composition, cured product of resin, prepreg and fiber-reinforced composite material
JPWO2020008847A1 (en) Epoxy resin composition for fiber reinforced composite material, fiber reinforced composite material and its manufacturing method
JP4475880B2 (en) Epoxy resin composition
JP4428978B2 (en) Epoxy resin composition
JPH0639519B2 (en) Epoxy resin composition and prepreg
JP5842395B2 (en) Epoxy resin composition for fiber reinforced composite materials
US4528342A (en) Epoxy resin compositions
JP2007284545A (en) Epoxy resin composition for fiber-reinforced composite material
JP2006291094A (en) Epoxy resin composition for reinforced composite material
JP2006291093A (en) Epoxy resin composition for fiber-reinforced composite material
US5151471A (en) Epoxy matrix resin formulations with improved storage stability containing powdered diamine dispersions
JPS6366242A (en) Air-permeating material
JP6961912B2 (en) Epoxy resin compositions, fiber reinforced composites, moldings and pressure vessels
JPH11279261A (en) Heat-resistant epoxy resin composition for fiber-reinforced composite material
US5244719A (en) Prepreg with improved room temperature storage stability
JP2003206332A (en) Epoxy resin composition for composite material and composite material using the same
JP4344662B2 (en) Epoxy resin composition, prepreg and molded body, and method for producing epoxy resin composition
JPH03243619A (en) Epoxy resin composition
JP3517468B2 (en) Carbon fiber reinforced composite material
JPH0517670A (en) Thermosetting resin composition