JPS60197723A - Composite material - Google Patents

Composite material

Info

Publication number
JPS60197723A
JPS60197723A JP5116584A JP5116584A JPS60197723A JP S60197723 A JPS60197723 A JP S60197723A JP 5116584 A JP5116584 A JP 5116584A JP 5116584 A JP5116584 A JP 5116584A JP S60197723 A JPS60197723 A JP S60197723A
Authority
JP
Japan
Prior art keywords
composite material
epoxy resin
polyethylene glycol
modified peg
modified
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.)
Granted
Application number
JP5116584A
Other languages
Japanese (ja)
Other versions
JPS6320449B2 (en
Inventor
Hiroyuki Fukuda
博之 福田
Kazuharu Shimizu
一治 清水
Tadahide Sato
佐藤 忠秀
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP5116584A priority Critical patent/JPS60197723A/en
Publication of JPS60197723A publication Critical patent/JPS60197723A/en
Publication of JPS6320449B2 publication Critical patent/JPS6320449B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27BSAWS FOR WOOD OR SIMILAR MATERIAL; COMPONENTS OR ACCESSORIES THEREFOR
    • B27B17/00Chain saws; Equipment therefor
    • B27B17/0033Devices for attenuation of vibrations

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Forests & Forestry (AREA)
  • Reinforced Plastic Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)

Abstract

PURPOSE:A composite material which has high vibration-damping property and can be used at higher temperature, comprising a reinforcing fiber and an epoxy resin containing modified polyethylene glycol. CONSTITUTION:A composite material comprising a reinforcing fiber (e.g., carbon fiber or glass fiber) and an epoxy resin (e.g., bisphenol A-derived epoxy resin) containing 10-40wt% amino group- or carboxyl group-terminated polyethylene glycol (hereinafter, abbreviated as modified PEG). This composite material can retain high vibration-damping property at high temperatures without exudation of the modified PEG because an epoxy resin containing polyethylene glycol having the modified PEG is used as the matrix resin. Besides, its strength and modulus are not less than those of a conventional composite material. Therefore, this composite material can be used effectively in the production of car stereo loud- speaker boxes, handles of electric drills, handles of chain saws, etc., for parts of an artificial satellite or as a structural material for automobiles, ships, etc.

Description

【発明の詳細な説明】 (イ)この発明の技術分野 この発明は複合材料に関し、さらに詳しくは、補強繊維
と樹脂との複合材料に関する。
DETAILED DESCRIPTION OF THE INVENTION (a) Technical Field of the Invention The present invention relates to a composite material, and more particularly to a composite material of reinforcing fibers and resin.

(ロ)従来技術とその欠点 補強繊維と樹脂との複合材料は、近年、たとえばゴルフ
シャフト、テニスラケットなどのスポーツ用途、スピー
カコーンやスピーカボックスなどの音響用途、ギターや
バイオリンの裏甲板や響板などの楽器用途といったよう
に、極めて広範な分野で使用されている。しかして、そ
のような用途においでは、はとんど例外なく高い振動減
衰性が要求されている。
(b) Conventional technology and its drawbacks Composite materials of reinforcing fibers and resins have been developed in recent years for sports applications such as golf shafts and tennis rackets, for acoustic applications such as speaker cones and speaker boxes, and for back decks and soundboards of guitars and violins. It is used in an extremely wide range of fields, such as musical instruments. However, in such applications, without exception, high vibration damping properties are required.

そのような高振動減衰性複合材料としては、たとえば特
開昭54−113299号公報に記載されているような
ものが知られている。この従来の複合材料は、その、い
わゆるマトリクス樹脂に、それ自体高い振動減衰性を有
するポリエチレングリコールを混入し、もって複合材料
の振動減衰性を向上せんとするものである。しかしなが
ら、かかる従来の複合材料は、室温程度の温度ではそれ
ほど問題ないものの、高温になるとポリエチレングリコ
ールが流れ出てくる、つまり振動減衰性が低下してくる
という欠点があり、せいぜい40’C程度までの領域に
おいて使用し得るにすぎない。
As such a high vibration damping composite material, for example, the one described in Japanese Patent Application Laid-Open No. 113299/1984 is known. In this conventional composite material, polyethylene glycol, which itself has high vibration damping properties, is mixed into the so-called matrix resin, thereby improving the vibration damping properties of the composite material. However, although such conventional composite materials do not have much of a problem at temperatures around room temperature, they have the disadvantage that polyethylene glycol flows out at high temperatures, in other words, the vibration damping properties decrease, and at most temperatures up to about 40'C. It can only be used in the area.

(ハ)この発明の目的 この発明の目的は、従来の複合材料の上記欠点を解決し
、高い振動減衰性をもち、かつより高温でも使用するこ
とができる複合材料を提供するにある。
(c) Purpose of the Invention The purpose of the present invention is to provide a composite material which solves the above-mentioned drawbacks of conventional composite materials, has high vibration damping properties, and can be used even at higher temperatures.

(ニ)この発明の構成 上記目的を達成するために、この発明においては、補強
繊維と樹脂からなる複合材料であって、かつ前記樹脂は
、末端基としてアミノ基またはカルボキシル基をもつポ
リエチレングリコールを10〜40重川%含む用ポキシ
樹脂からなることを特徴とする複合材料が提供される。
(d) Structure of the Invention In order to achieve the above object, the present invention provides a composite material consisting of reinforcing fibers and a resin, and the resin contains polyethylene glycol having an amino group or a carboxyl group as a terminal group. A composite material is provided, characterized in that it is made of a poxy resin containing 10 to 40%.

この発明をさらに詳細に説明するに、この発明の複合材
料は、補強繊維と樹脂とを複合してなる。
To explain this invention in more detail, the composite material of this invention is made by combining reinforcing fibers and resin.

上記補強繊維は、m雑強化プラスチックの補強繊維とし
て通常用いられている炭素繊維、ガラス繊維、有機高弾
性繊維(たとえば、ポリアラミド繊維)などの高強痩、
高弾性繊維である。なかでも、炭素繊維が最も好ましく
使用される。もっとも、これらの補強繊維は異なる2種
以上の繊維が併用されてもよいものである。
The above-mentioned reinforcing fibers include high-strength and thin fibers such as carbon fibers, glass fibers, and organic high-elastic fibers (e.g., polyaramid fibers), which are commonly used as reinforcing fibers for miscellaneous reinforced plastics.
Highly elastic fiber. Among them, carbon fiber is most preferably used. However, two or more different types of these reinforcing fibers may be used in combination.

また、上記樹脂は、エポキシ樹脂と、末端基としてアミ
ノ基またはカルボキシル基をもつポリエチレングリコー
ル(以下、変性PEGという)からなる。エポキシ樹脂
は、ビスフェノールA型、脂肪族型、フェノールノボラ
ック型など、いずれであってもよい。また、変性PEG
は、複合材料に高い振動減衰性を与えるもので、エポキ
シ樹脂との相溶性が高い、分子−400〜10000程
度のものが好ましく使用される。さらに好ましくは、分
子−400〜6000のものが使用される。
Further, the resin is composed of an epoxy resin and polyethylene glycol (hereinafter referred to as modified PEG) having an amino group or a carboxyl group as a terminal group. The epoxy resin may be of any type, such as bisphenol A type, aliphatic type, or phenol novolac type. In addition, modified PEG
gives high vibration damping properties to the composite material, and those having high compatibility with epoxy resins and having a molecular weight of about -400 to 10,000 are preferably used. More preferably, those having a molecular weight of -400 to -6000 are used.

そのような変性PEGの代表的例としては、アミノ基を
もつものでは三洋化成工業株式会社製゛PE G 40
00 D CA ”が、カルボキシル基をもつものでは
同社製°′イオネットY B −400”などがある。
A typical example of such modified PEG is PEG 40 manufactured by Sanyo Chemical Industries, Ltd., which has an amino group.
00D CA'' has a carboxyl group, such as 'Ionet YB-400'' manufactured by the same company.

エポキシ樹脂に対する変性PEGの混入量は10〜40
重量%である。すなわち、10重量%未満では高い振動
減衰性を有する複合材料が得られない。また、40重量
%を越えると複合材料の剛性が著しく低下し、使用に耐
えなくなる。より好ましい混入量は10〜25重偵%で
ある。
The amount of modified PEG mixed into the epoxy resin is 10 to 40
Weight%. That is, if it is less than 10% by weight, a composite material with high vibration damping properties cannot be obtained. Moreover, if it exceeds 40% by weight, the rigidity of the composite material will be significantly reduced, making it unusable. A more preferable amount is 10 to 25%.

この発明の複合材料は、補強111Hと、所望−の変性
PEGを混入したエポキシ樹脂とを複合し、次いでその
複合体を1oo〜120’Cに加熱して変性PEGをエ
ポキシ樹脂と結合し、以下、常法にしたがってエポキシ
樹脂を硬化させることによって製造する。エポキシ樹脂
の硬化温度は130〜180℃である。もっとも、この
発明においては、変性PEGをエポキシ樹脂と結合した
後に補強繊維と複合してもよい。
The composite material of the present invention is produced by combining the reinforcement 111H with an epoxy resin mixed with a desired modified PEG, and then heating the composite to 100 to 120'C to bond the modified PEG with the epoxy resin. , manufactured by curing epoxy resin according to conventional methods. The curing temperature of the epoxy resin is 130 to 180°C. However, in the present invention, the modified PEG may be combined with the epoxy resin and then composited with reinforcing fibers.

(ホ)この発明の効果 この発明の複合材料は、いわゆるマトリクス樹脂として
、変性PEG、つまり末端基としてアミノ基またはカル
ボキシル基をもつポリエチレングリコールを10〜40
重量%含むエポキシ樹脂を使用しているからして、高温
で使用しても変性PEGが流れ出ることがなく、高い振
動減衰性を維持できる。しかも、強度や弾性率も従来の
複合材料にくらべて優るとも劣らない。そのため、この
発明の複合材料は、使用中に高温になる可能性があり、
しかも高い振動減衰性が要求される用途に特に適してい
る。たとえば、カーステレオのスピーカーボックスの構
成材料として使用すれば、炎天下の高温の車内において
も共振のない明瞭な音が楽しめる。また、たとえばチェ
ーンソーや電動ドリルの柄に使用すると、モーターの加
熱によって高温になっても振動が抑制され、振動による
職業病の防止に役立つ。さらに、人工衛星の部品に使用
すると、摩擦熱などが加わっても振動が抑制され、姿勢
制御を正確に行えるようになる。さらに、自動車や船舶
などの構造材料として使用することもできる。もちろん
、上述したスポーツ用途や楽器用途に使用しても何ら差
し支えない。
(e) Effects of the present invention The composite material of the present invention contains modified PEG, that is, polyethylene glycol having an amino group or a carboxyl group as a terminal group, in a concentration of 10 to 40% as a so-called matrix resin.
Since the epoxy resin containing % by weight is used, the modified PEG does not flow out even when used at high temperatures, and high vibration damping properties can be maintained. Moreover, its strength and elastic modulus are comparable to those of conventional composite materials. Therefore, the composite material of this invention can reach high temperatures during use.
Furthermore, it is particularly suitable for applications requiring high vibration damping properties. For example, if it is used as a component of a car stereo speaker box, you can enjoy clear sound without resonance even in the hot car interior under the scorching sun. Furthermore, when used on the handles of chainsaws and electric drills, for example, vibrations are suppressed even when the motors heat up to high temperatures, helping to prevent occupational diseases caused by vibrations. Furthermore, when used in parts of artificial satellites, vibrations are suppressed even when frictional heat is applied, allowing for accurate attitude control. Furthermore, it can also be used as a structural material for automobiles, ships, etc. Of course, there is no problem in using it for sports or musical instruments as described above.

実施例1 100qのエポキシ樹脂“エピコート” 828(油化
シェルエポキシ株式会社製)に20gの変性PEG ”
PEG4000DCA” (三洋化成工業株式会社製)
を加え、約120℃で約2時間加熱して変性PEGをエ
ポキシ樹脂と結合した後約70℃まで降温し、硬化剤と
して3oのジシアンジアミド/N−3,4ジクロロフェ
ニレンN=−ジメヂルウレアを加え、マトリクス樹脂を
得た。
Example 1 100q of epoxy resin “Epicote” 828 (manufactured by Yuka Shell Epoxy Co., Ltd.) and 20g of modified PEG”
PEG4000DCA” (manufactured by Sanyo Chemical Industries, Ltd.)
was added and heated at about 120°C for about 2 hours to bond the modified PEG with the epoxy resin, then the temperature was lowered to about 70°C, and 3o dicyandiamide/N-3,4 dichlorophenylene N=-dimedylurea was added as a curing agent. A matrix resin was obtained.

次に、東し株式会社製炭素繊随゛トレカ″T−300(
ストランド数: 3000本)を一方向に互に並行かつ
シート状に引き揃えたものに上記マトリクス樹脂を含浸
した後、炭素繊維の方向を揃えて300m5角に截断し
た。
Next, we will introduce the carbon fiber trading card “T-300” manufactured by Toshi Co., Ltd.
After impregnating the above matrix resin into a sheet made of 3,000 strands arranged in parallel to each other in one direction, the carbon fibers were cut into 5 squares of 300 m with the directions aligned.

次に、上記裁断片を炭素繊維の方向を揃えて金型内に3
枚積層し、約10Ko/cm2の圧力を加えながら約1
40℃で約2時間加熱してマトリクス樹脂を硬化させ、
炭素繊維の体積含有率が約60%であり、かつ厚みが2
11111であるこの発明の複合材料を得た。
Next, place the cut pieces into the mold 3 times with the direction of the carbon fibers aligned.
Laminate the sheets, apply a pressure of about 10 Ko/cm2, and
Heat at 40°C for about 2 hours to harden the matrix resin.
The volume content of carbon fiber is approximately 60%, and the thickness is 2
11111 was obtained.

一ト記複合材料について、引張弾性率と、20℃、44
0Hzにおける振動減衰係数と、変性PEGの流出量を
測定したところ、引張弾性率は約13゜000KO/+
na2であり、振動減衰係数は約0゜45X10−2で
あり、変性PEGの流出量はほとんど零であった。なお
、振動減衰係数は振動リード法によって測定した。また
、変性PEGの流出量は、複合材料を沸騰水に約20時
間浸漬し、浸漬する前の重量Wと、浸漬した後の重1w
から、式(W−W)Xl 00/Wによりめた。つまり
、変性PEGの流出量は、複合材料を約100℃で使用
した場合に相当する。
Regarding composite materials, tensile modulus and 20℃, 44
When we measured the vibration damping coefficient at 0Hz and the outflow amount of modified PEG, the tensile modulus was approximately 13°000KO/+
na2, the vibration damping coefficient was about 0°45×10-2, and the amount of modified PEG flowing out was almost zero. Note that the vibration damping coefficient was measured by the vibration lead method. In addition, the amount of outflow of modified PEG is calculated by immersing the composite material in boiling water for about 20 hours, and calculating the weight W before immersion and the weight 1 W after immersion.
Therefore, it was determined by the formula (W-W)Xl 00/W. In other words, the amount of modified PEG flowing out corresponds to the case where the composite material is used at about 100°C.

実施例2 上記実施例1で使用したエポキシ樹脂1ooqに、末端
基としてカルボキシル基をもつ変性PEG(分子量:約
400)を20o混入したほかは実施例1と全く同様に
してこの発明の複合材料を得た。
Example 2 A composite material of the present invention was produced in exactly the same manner as in Example 1, except that 20 grams of modified PEG (molecular weight: about 400) having a carboxyl group as a terminal group was mixed into 1 ooq of the epoxy resin used in Example 1 above. Obtained.

次に、上記各複合材料について、実施例1と同様に引張
弾性率、振動減衰係数、変性PEGの流出量を測定した
ところ、引張弾性率は約13,000 K Q /’m
i2であり、振動減衰係数は約0.40X10−2であ
り、変性PEGの流出量はほとんど零であづた。
Next, for each of the above composite materials, the tensile modulus, vibration damping coefficient, and outflow amount of modified PEG were measured in the same manner as in Example 1, and the tensile modulus was approximately 13,000 K Q /'m.
i2, the vibration damping coefficient was approximately 0.40X10-2, and the amount of modified PEG flowing out was almost zero.

比較例 変性PEGの代わりに三洋化成工業株式会社製ポリエチ
レングリコール゛’PEG4000” (分子量:約4
000)を使用したほかは実施例1と全く同様にして、
複合材料を得た。
Comparative Example Instead of modified PEG, polyethylene glycol ``PEG4000'' manufactured by Sanyo Chemical Industries, Ltd. (molecular weight: approximately 4
000) was used in exactly the same manner as in Example 1,
A composite material was obtained.

この複合材料について実施例1と同様の試験をしたとこ
ろ、引張弾性率は約13.100Kq/■2であり、ま
た振動減衰係数は約0.46X1Q−2で実施例1.2
のそれとそれほど変わらなかった。しかし、ポリエチレ
ングリコールの流出量は約5重量%もあった。このこと
は、この複合材料を高温で使用するとポリエチレングリ
コールが流出し、その分だけ振動減衰性が低下してくる
ことを示している。
When this composite material was subjected to the same test as in Example 1, the tensile modulus was approximately 13.100Kq/■2, and the vibration damping coefficient was approximately 0.46X1Q-2, which was the same as in Example 1.2.
It wasn't that different from that. However, the amount of polyethylene glycol flowing out was about 5% by weight. This indicates that when this composite material is used at high temperatures, polyethylene glycol flows out, and the vibration damping properties decrease accordingly.

特許出願人 東し株式会社Patent applicant: Toshi Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 補強繊維と樹脂からなる複合材料であって、かつ前記樹
脂は、末端基としてアミノ基またはカルボキシル基をも
つポリエチレングリコールを10〜40重量%含むエポ
キシ樹脂からなることを特徴とする複合材料。
1. A composite material comprising reinforcing fibers and a resin, wherein the resin is an epoxy resin containing 10 to 40% by weight of polyethylene glycol having an amino group or a carboxyl group as a terminal group.
JP5116584A 1984-03-19 1984-03-19 Composite material Granted JPS60197723A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5116584A JPS60197723A (en) 1984-03-19 1984-03-19 Composite material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5116584A JPS60197723A (en) 1984-03-19 1984-03-19 Composite material

Publications (2)

Publication Number Publication Date
JPS60197723A true JPS60197723A (en) 1985-10-07
JPS6320449B2 JPS6320449B2 (en) 1988-04-27

Family

ID=12879207

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5116584A Granted JPS60197723A (en) 1984-03-19 1984-03-19 Composite material

Country Status (1)

Country Link
JP (1) JPS60197723A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0333297A (en) * 1988-04-01 1991-02-13 Sanyo Kokusaku Pulp Co Ltd Primarily treated base paper for electrical insulating laminated board, production thereof and electrical insulating laminated board using the same
CN115010904A (en) * 2022-07-04 2022-09-06 青岛爱尔家佳新材料股份有限公司 Organosilicon modified waterborne epoxy emulsion, waterborne epoxy primer and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0468546U (en) * 1990-10-25 1992-06-17

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639928A (en) * 1970-11-27 1972-02-08 Jefferson Chem Co Inc Accelerator combination for epoxy curing
JPS5413597A (en) * 1977-06-30 1979-02-01 Texaco Development Corp Bisureide additive of polyoxyalkylene polyamine and curable epoxy resin composition using it
JPS5491598A (en) * 1977-12-27 1979-07-20 Texaco Development Corp Hardener for epoxy resin and rapidly hardening method of said epoxy resin

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3639928A (en) * 1970-11-27 1972-02-08 Jefferson Chem Co Inc Accelerator combination for epoxy curing
JPS5413597A (en) * 1977-06-30 1979-02-01 Texaco Development Corp Bisureide additive of polyoxyalkylene polyamine and curable epoxy resin composition using it
JPS5491598A (en) * 1977-12-27 1979-07-20 Texaco Development Corp Hardener for epoxy resin and rapidly hardening method of said epoxy resin

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0333297A (en) * 1988-04-01 1991-02-13 Sanyo Kokusaku Pulp Co Ltd Primarily treated base paper for electrical insulating laminated board, production thereof and electrical insulating laminated board using the same
JPH0457799B2 (en) * 1988-04-01 1992-09-14 Sanyo Kokusaku Pulp Co
CN115010904A (en) * 2022-07-04 2022-09-06 青岛爱尔家佳新材料股份有限公司 Organosilicon modified waterborne epoxy emulsion, waterborne epoxy primer and preparation method thereof
CN115010904B (en) * 2022-07-04 2023-12-19 青岛爱尔家佳新材料股份有限公司 Organosilicon modified aqueous epoxy emulsion, aqueous epoxy primer and preparation method thereof

Also Published As

Publication number Publication date
JPS6320449B2 (en) 1988-04-27

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