JPH03187726A - Fiber-reinforced resin molded item and preparation thereof - Google Patents
Fiber-reinforced resin molded item and preparation thereofInfo
- Publication number
- JPH03187726A JPH03187726A JP1327662A JP32766289A JPH03187726A JP H03187726 A JPH03187726 A JP H03187726A JP 1327662 A JP1327662 A JP 1327662A JP 32766289 A JP32766289 A JP 32766289A JP H03187726 A JPH03187726 A JP H03187726A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- resin
- elastic body
- mold
- reinforced
- 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
- 229920005989 resin Polymers 0.000 title claims abstract description 69
- 239000011347 resin Substances 0.000 title claims abstract description 69
- 239000000835 fiber Substances 0.000 claims abstract description 37
- 239000011159 matrix material Substances 0.000 claims abstract description 15
- 239000011162 core material Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000006260 foam Substances 0.000 abstract description 6
- 239000003365 glass fiber Substances 0.000 abstract description 6
- 238000000465 moulding Methods 0.000 abstract description 5
- 229920001187 thermosetting polymer Polymers 0.000 abstract description 5
- 238000010107 reaction injection moulding Methods 0.000 abstract description 4
- 239000012779 reinforcing material Substances 0.000 abstract description 4
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 4
- 238000003825 pressing Methods 0.000 abstract description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract description 2
- 229920000049 Carbon (fiber) Polymers 0.000 abstract description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052796 boron Inorganic materials 0.000 abstract description 2
- 239000004917 carbon fiber Substances 0.000 abstract description 2
- 239000000805 composite resin Substances 0.000 abstract description 2
- 239000004745 nonwoven fabric Substances 0.000 abstract description 2
- 239000010703 silicon Substances 0.000 abstract description 2
- 229910052710 silicon Inorganic materials 0.000 abstract description 2
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 11
- 230000002787 reinforcement Effects 0.000 description 9
- 239000002994 raw material Substances 0.000 description 8
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 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 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000582 polyisocyanurate Polymers 0.000 description 1
- 239000011495 polyisocyanurate Substances 0.000 description 1
- -1 rubber-like bodies Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、繊維強化樹脂成形体およびその製造方法に関
するものであり、詳しくは、剛性が高く、しかも表面平
滑性の優れた繊維強化樹脂成形体およびその製造方法に
関するものである。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a fiber-reinforced resin molded article and a method for producing the same, and more specifically, a fiber-reinforced resin molded article with high rigidity and excellent surface smoothness. The present invention relates to bodies and methods for producing the same.
(従来の技術)
近年、繊維強化樹脂成形体が自動車用外板等に用いられ
るようになって、その剛性や表面平滑性が重要視される
ようになってきた。特に、表面の平滑性は、自動車分野
に限らず、商品としての美観を保つ上で重要である。(Prior Art) In recent years, fiber-reinforced resin molded bodies have been used for automobile outer panels and the like, and their rigidity and surface smoothness have become important. In particular, surface smoothness is important not only in the automobile field but also in maintaining the aesthetic appearance of products.
一般に、型の中に繊維強化材を載置し、型を閉じた後、
樹脂を注入、硬化して製造する繊維強化樹脂成形体にお
いて、その表面には型キャビティの表面がそのまま転写
されるわけではない。これは、硬化時に樹脂の収縮が起
こり、ガラス繊維が表面に浮き出るようになるからであ
り、この場合の表面平滑性はあまり良好とは言えない。Generally, after placing the fiber reinforcement in the mold and closing the mold,
In a fiber-reinforced resin molded article manufactured by injecting and curing resin, the surface of the mold cavity is not directly transferred to the surface thereof. This is because the resin shrinks during curing and the glass fibers come to stand out on the surface, and the surface smoothness in this case cannot be said to be very good.
ここで、収縮とは、硬化収縮と熱収縮を含む。Here, shrinkage includes curing shrinkage and heat shrinkage.
かかる繊維強化樹脂の表面平滑性を改良する方法として
は、樹脂の改良、製法の改良、二次加工等が知られてい
る。As methods for improving the surface smoothness of such fiber-reinforced resins, improvements in resins, improvements in manufacturing methods, secondary processing, etc. are known.
(発明が解決しようとする課題)
しかしながら、第一の方法としては、樹脂の収縮率を低
下させるよう改質することであり、化学的改質、物理的
改質(フィラーの添加等)が挙げられるが、表面平滑性
の向上の程度には限度かある。・
また、第二の方法としては、ゲルコート法、インモール
ド・コーティング法、加圧ゲル化法等が挙げられるが、
製法が複雑となり、有利とは言えない。また、樹脂中に
溶解したガスの圧力を利用して収縮を抑制する方法があ
るが、条件のコントロールが難しく、有利とは言えない
。(Problem to be solved by the invention) However, the first method is to modify the resin to reduce its shrinkage rate, and examples include chemical modification and physical modification (addition of fillers, etc.). However, there is a limit to the degree of improvement in surface smoothness.・Also, the second method includes gel coating method, in-mold coating method, pressure gelling method, etc.
The manufacturing method is complicated and cannot be said to be advantageous. There is also a method of suppressing shrinkage using the pressure of gas dissolved in the resin, but it is difficult to control the conditions and cannot be said to be advantageous.
さらに、第三の方法としては、成形体上に塗装を施すこ
とが挙げられるが、コストが高くつきやはり有利とは言
えない。Furthermore, a third method is to apply a coating onto the molded body, but this method is expensive and cannot be said to be advantageous.
(課題を解決するための手段)
そこで本発明者等は、このような事情に鑑み、鋭意検討
した結果、マトリックス樹脂を実質的に含浸しない弾性
体を核材として、その周囲に繊維強化樹脂複合材を配置
することにより、かがる課題を解消できることを見いだ
し、本発明を完成した。(Means for Solving the Problems) In view of the above circumstances, the inventors of the present invention have made extensive studies and found that an elastic body that is not substantially impregnated with matrix resin is used as a core material, and a fiber-reinforced resin composite is used around it. It was discovered that the problem of overcasting could be solved by arranging the materials, and the present invention was completed.
すなわち、本発明の目的は、剛性が高く、しがも表面平
滑性の優れた繊維強化樹脂成形体、およびその製造方法
を提供するものである。That is, an object of the present invention is to provide a fiber-reinforced resin molded article having high rigidity and excellent surface smoothness, and a method for producing the same.
そして、その目的は、
(1)マトリックス樹脂を実質的に含浸しない圧縮状態
にある弾性体を核材とし、その周囲に配置された繊維強
化材、および該繊維強化材に含浸されたマトリックス樹
脂から構成されることを特徴とする繊維強化樹脂成形体
。The purpose is to: (1) use an elastic body in a compressed state that is not substantially impregnated with matrix resin as a core material, fiber reinforcement material arranged around it, and matrix resin impregnated in the fiber reinforcement material; A fiber-reinforced resin molded article comprising:
および、
(2)マトリックス樹脂を実質的に含浸しない弾性体、
およびその周囲に該弾性体に接するように配置された繊
維強化材を型の中に載置し、型を閉じた後、該弾性体を
圧縮したままマトリックス樹脂を注入して加熱硬化する
ことを特徴とする繊維強化樹脂成形体の製造方法。and (2) an elastic body that is not substantially impregnated with matrix resin;
A fiber reinforced material placed around the elastic body in contact with the elastic body is placed in a mold, and after the mold is closed, a matrix resin is injected and heated to harden the elastic body while keeping it compressed. A method for producing a characteristic fiber-reinforced resin molded article.
により、容易に達成される。easily achieved.
以下に、本発明をより詳細に説明する。The present invention will be explained in more detail below.
本発明で言う弾性体とは、弾性を有するもの全てを含み
、具体的には発泡体、ゴム状体、不織布、マット等が挙
げられ、型の中で樹脂の硬化が完了するまで上下面に隣
接して配置された繊維強化材を型キヤビテイ表面に押し
つける機能を有するものである。尚、前記隣接は、直接
接しておらず、中間層が存在していても、繊維強化材を
型キヤビテイ表面に押しつける圧力を伝達しうる状態を
含む。弾性体として発泡体等を用いる場合、樹脂が発泡
体の中まで含浸すると弾性の低下を引き起こすので、含
浸しない方が好ましい。表面のスキン層あるいは圧力を
伝達する中間層により、含浸を阻止するものであっても
よい。弾性体の圧縮力としては、少なくともその周囲に
配置された繊維強化材を型の表面に押しつけるだけの力
を有し、しかも型が開かないよう型締め圧より低い力で
あることが必要であり、具体的には0.05〜20kg
f/cm’、好ましくは0.1〜10kgf/am2が
好適である。The elastic body referred to in the present invention includes anything that has elasticity, and specifically includes foam, rubber-like bodies, nonwoven fabrics, mats, etc. It has the function of pressing the adjacent fiber reinforcement material against the mold cavity surface. Note that the above-mentioned adjacency includes a state in which pressure for pressing the fiber reinforcement material against the mold cavity surface can be transmitted even if there is no direct contact and an intermediate layer is present. When a foam or the like is used as the elastic body, impregnation of the resin into the foam causes a decrease in elasticity, so it is preferable not to impregnate the foam. Impregnation may be prevented by a surface skin layer or an intermediate layer that transmits pressure. The compressive force of the elastic body must be at least enough to press the fiber reinforcement placed around it against the surface of the mold, and must also be lower than the mold clamping pressure to prevent the mold from opening. , specifically 0.05 to 20 kg
f/cm', preferably 0.1 to 10 kgf/am2.
圧縮倍率については、硬化収縮により圧縮力が上記範囲
より小さくならない範囲であれば特に限定されない。The compression ratio is not particularly limited as long as the compression force does not become smaller than the above range due to curing shrinkage.
本発明で言う繊維強化樹脂とは、繊維で強化された樹脂
であり、繊維としては、無機、有機から選ばれる材料か
らなり、例えば、ガラス繊維、炭素繊維、アルミナ繊維
、ボロン繊維、珪素繊維、芳香族ポリアミド繊維、ポリ
エステル繊維等が挙げられる。繊維の長さは、限定され
ないが、機械的強度を高くするためには、長い方が好ま
しい。The fiber-reinforced resin referred to in the present invention is a resin reinforced with fibers, and the fibers are made of materials selected from inorganic and organic materials, such as glass fibers, carbon fibers, alumina fibers, boron fibers, silicon fibers, Examples include aromatic polyamide fibers and polyester fibers. Although the length of the fiber is not limited, the longer the fiber is, the more preferable it is in order to increase the mechanical strength.
繊維強化材の形態としては、マット、織物、あるいはこ
れらを組み合わせたものが好ましく用いられる。The form of the fiber reinforcement material is preferably a mat, a woven fabric, or a combination thereof.
本発明で言うマトリックス樹脂とは、反応射出成形機に
よって成形可能な熱可塑性、熱硬化性、あるいはこれら
を組み合わせた樹脂である。これらの樹脂は、液状の樹
脂原料の形態で型の中に注入される。液状樹脂原料とは
、前記樹脂の原料となる二液、あるいは三液性のもので
あり、これらを衝突混合させて硬化させることが出来る
。樹脂原料の粘度は、型温や混合比に依存するが、混合
後、注入する時点で低いほど好適であり、具体的には5
0cp以下が好ましい。硬化速度は型内に充てんする時
は遅く、充てんが完了した後は速やかに硬化することが
好ましい。The matrix resin referred to in the present invention is a thermoplastic resin, a thermosetting resin, or a combination thereof that can be molded by a reaction injection molding machine. These resins are injected into the mold in the form of liquid resin raw materials. The liquid resin raw material is a two-component or three-component material that is a raw material for the resin, and can be hardened by impact-mixing these materials. The viscosity of the resin raw material depends on the mold temperature and mixing ratio, but the lower it is at the time of injection after mixing, the better.
It is preferably 0 cp or less. It is preferable that the curing speed is slow when filling the mold, and that it hardens quickly after filling is completed.
具体的には、硬化時間として10分以下、好ましくは5
分以下、より好ましくは3分以下がよい。本発明の樹脂
としては、エポキシ、ビニルエステル、不飽和ポリエス
テル、フェノール、ビスマレイミド、ウレタン、ポリウ
レア、ポリイソシアヌレート等の熱硬化性樹脂、ポリア
ミド、ポリカーボネイト等の熱可塑性樹脂が挙げられる
。また、ノルボルネン型重合性モノマー、およびアリル
、ビニル、アクリル、メタクリル型の炭素−炭素二重結
合を有するモノマー、オリゴマーから重合される熱硬化
性樹脂も含まれる。これらの樹脂に反応性希釈剤、触媒
、内部離型剤等の添加物を適宜添加してもよい。Specifically, the curing time is 10 minutes or less, preferably 5 minutes.
The time is preferably 3 minutes or less, more preferably 3 minutes or less. Examples of the resin of the present invention include thermosetting resins such as epoxy, vinyl ester, unsaturated polyester, phenol, bismaleimide, urethane, polyurea, and polyisocyanurate, and thermoplastic resins such as polyamide and polycarbonate. Also included are thermosetting resins polymerized from norbornene type polymerizable monomers, and monomers and oligomers having allyl, vinyl, acrylic, and methacrylic type carbon-carbon double bonds. Additives such as a reactive diluent, a catalyst, and an internal mold release agent may be appropriately added to these resins.
成形体の構造としては、繊維強化材の少なくとも一部が
周囲を囲んでいることが好ましい。すなわち、繊維強化
材の寸法よりも弾性体の寸法を小さ目にし、弾性体の外
周部の少なくとも一部において上下の繊維強化材の少な
くとも一部が相互の剪断変形を拘束するのに十分あるい
はそれ以上の強度を持つように一体に成形されることが
好ましい。この様な成形体構造の例として、図1の様な
形態が挙げられる。図1において、1は弾性体、2,2
′は、マトリックス樹脂を含浸した繊維強化材である。As for the structure of the molded body, it is preferable that at least a portion of the fiber reinforcement material surrounds the periphery. In other words, the dimensions of the elastic body are made smaller than the dimensions of the fiber reinforced material, and at least a portion of the upper and lower fiber reinforced materials in at least part of the outer periphery of the elastic body are made sufficient or larger than the dimensions of the fiber reinforced material to restrain mutual shear deformation. It is preferable that they be integrally molded to have a strength of . An example of such a molded body structure is the form shown in FIG. 1. In Figure 1, 1 is an elastic body, 2, 2
' is a fiber reinforced material impregnated with matrix resin.
これにより両側の繊維強化樹脂の相互に独立な動きが拘
束され、強固なサンドイッチ構造体を形成することがで
きる。もし、両側の繊維強化材が拘束されていなかった
り拘束部分の強度が不十分であったりすると、成形後、
弾性体が膨らんで板厚が大きくなったり、負荷を受けた
時、弾性体の部分で剪断破壊を引き起こしたりして、好
ましくない。This restricts mutually independent movement of the fiber reinforced resins on both sides, making it possible to form a strong sandwich structure. If the fiber reinforcement materials on both sides are not restrained or the strength of the restrained parts is insufficient, after molding,
This is undesirable because the elastic body swells and the plate thickness increases, or when a load is applied, shear failure occurs in the elastic body.
次ぎに、本発明の繊維強化樹脂成形体を製造する方法を
説明する。Next, a method for manufacturing the fiber-reinforced resin molded article of the present invention will be explained.
型としては、金属製、樹脂製のいずれを用いても良い。The mold may be made of metal or resin.
型キャビティの表面は、研磨等により平滑に仕上げてお
くことが好ましい。これは、本発明方法に従って成形体
の表面平滑性を良好にする上で重要であり、また、成形
時の離型性を良くする上でも重要である。The surface of the mold cavity is preferably finished smooth by polishing or the like. This is important in improving the surface smoothness of the molded article according to the method of the present invention, and is also important in improving the mold releasability during molding.
型の中には、弾性体を核材として、その周囲に所定量の
繊維強化材を所定の位置に載置する。繊維強化材は、マ
ットのみ、織物のみを一枚以上積層して載置してもよい
し、これらを適宜組み合わせて載置してもよい。Inside the mold, an elastic body is used as a core material, and a predetermined amount of fiber reinforcing material is placed around it at a predetermined position. The fiber reinforcing material may be placed by laminating one or more mats or only woven fabrics, or may be placed by combining these as appropriate.
この後、型を閉じ、液状樹脂原料を注入する。After this, the mold is closed and the liquid resin raw material is injected.
液状樹脂原料としては、前記の熱硬化性樹脂、熱可塑性
樹脂、添加物、およびこれらを組み合わせたものの中か
ら選ばれる。注入方法としては、反応射出成形の常法に
より行い、温度、圧力等の操作条件は個々の樹脂の性状
、成形体の要求性能等により適宜法められる。注入量は
、成形する成形体の体積、弾性体の体積、繊維含有率等
により決まる。ここで、弾性体の中には、実質的に樹脂
を含有しないことが重要である。これは、弾性体の中の
樹脂の硬化が進行するにしたがって、弾性体として機能
しなくなるからである。The liquid resin raw material is selected from the above thermosetting resins, thermoplastic resins, additives, and combinations thereof. The injection method is a conventional reaction injection molding method, and operating conditions such as temperature and pressure are determined as appropriate depending on the properties of the individual resin, the required performance of the molded product, etc. The injection amount is determined by the volume of the molded body to be molded, the volume of the elastic body, the fiber content, etc. Here, it is important that the elastic body does not substantially contain resin. This is because as the resin in the elastic body hardens, it ceases to function as an elastic body.
注入が完了したら、そのまま密閉した型の中で所定の温
度条件下で硬化させ、硬化が完了したら、樹脂のガラス
転移温度以下で型を開き、成形体を取り出す。樹脂のガ
ラス転移温度以上であると、弾性体の反発力により成形
体が変形する恐れがあるので好ましくない。Once the injection is complete, the resin is cured in a sealed mold under predetermined temperature conditions. Once curing is complete, the mold is opened at a temperature below the glass transition temperature of the resin and the molded product is taken out. If the temperature is higher than the glass transition temperature of the resin, the molded article may be deformed due to the repulsive force of the elastic body, which is not preferable.
弾性体を挟み込むことにより、硬化の終了まで成形体の
表面を型キヤビテイ表面に押しつけることが可能となり
、樹脂の収縮による表面平滑性の低下を防止することが
出来る。この場合、注入の開始から硬化の完了まで成形
体の表面を型で加圧することが必要であり、樹脂の収縮
等により加圧できない状態にならないよう注意する必要
がある。また、型キャビティの形状が成形体表面にその
まま転写されるため、キャビティの表面性が良好である
ことが必要であることは言うまでもない。また、両側の
繊維強化樹脂層が剪断を阻止するよう少なくとも一部に
おいて拘束されるため、高い曲げ剛性を発揮できる。By sandwiching the elastic body, it is possible to press the surface of the molded article against the mold cavity surface until the end of curing, and it is possible to prevent a decrease in surface smoothness due to resin contraction. In this case, it is necessary to pressurize the surface of the molded body with a mold from the start of injection to the completion of curing, and care must be taken to ensure that the resin does not become unable to be pressurized due to shrinkage or the like. Furthermore, since the shape of the mold cavity is directly transferred to the surface of the molded product, it goes without saying that the cavity must have good surface properties. Furthermore, since the fiber reinforced resin layers on both sides are restrained at least in part to prevent shearing, high bending rigidity can be exhibited.
(実施例)
実施例1
型としては、盤面の大きさが、縦300mm、横300
mmで、キャビティの深さ3mmの金属製のものを用い
た。型キャビティの表面は研磨により#600に仕上げ
た。型の温度は120°Cに保った。樹脂原料としては
、ビスフェノールA型ジグリシジルエーテル(以下、A
と略記)とイソホロンジアミン(以下、Bと略記)を用
いた。繊維としては、縦295mm、横295mmで目
付は量450g/m’のガラス繊維マット、同じ< 1
58g/m2のガラス繊維織物を用いた。弾性体として
は、縦250mm、横250mm、厚さ1.5mmの硬
質発泡ウレタン(表面にスキン層あり)を用いた。(Example) Example 1 The size of the board surface is 300 mm in length and 300 mm in width.
A metal one with a cavity depth of 3 mm was used. The surface of the mold cavity was polished to #600. The temperature of the mold was maintained at 120°C. As a resin raw material, bisphenol A type diglycidyl ether (hereinafter referred to as A
) and isophoronediamine (hereinafter abbreviated as B) were used. The fibers are glass fiber mats with a length of 295 mm and a width of 295 mm and a basis weight of 450 g/m', the same < 1.
A 58 g/m2 glass fiber fabric was used. As the elastic body, a hard urethane foam (with a skin layer on the surface) with a length of 250 mm, a width of 250 mm, and a thickness of 1.5 mm was used.
前記型の中に、前記の弾性体を核材として、両側に前記
のガラスマットを各−枚配置し、さらにその両側に前記
のガラス織物を各−枚配置されるように積層して載置し
た。この後、型を閉じ、樹脂原料を重量比でB/A =
27/100となるよう反応射出成形機により型内に
注入した。10分後に型を冷却し、室温まで下がったと
ころで型を開き、成形体を取り出した。Inside the mold, with the elastic body as a core material, each sheet of the glass mat is placed on both sides, and each sheet of the glass fabric is stacked on both sides thereof. did. After this, the mold is closed and the weight ratio of the resin raw material is B/A =
It was injected into a mold using a reaction injection molding machine so that the ratio was 27/100. After 10 minutes, the mold was cooled, and when the temperature reached room temperature, the mold was opened and the molded product was taken out.
得られた成形体のサンドイッチ構造部の厚さは3mmで
あり、その表面の平滑性は前記型キャビティの研磨仕上
げそのままにきわめて良好であった。本成形体の表面形
状を触針式表面粗度計(小板研究所製“5urfcor
der SE −3F”)により測定し、図2に示した
。The thickness of the sandwich structure of the obtained molded body was 3 mm, and the surface smoothness was as good as the polished finish of the mold cavity. The surface shape of the molded body was measured using a stylus-type surface roughness meter ("5urfcor" manufactured by Koita Research Institute).
der SE-3F'') and shown in FIG.
比較例1
型キャビティの深さが2mmであること、弾性体を用い
ないこと以外は実施例と同様にして繊維強化樹脂成形体
を製造した。Comparative Example 1 A fiber-reinforced resin molded body was produced in the same manner as in Example except that the depth of the mold cavity was 2 mm and no elastic body was used.
得られた成形体の厚さは1.8mmであり、その表面の
樹脂層には、強化材として用いたガラス繊維の跡が浮き
上がって観察された。実施例1と同一条件で表面形状を
測定し、図3に示した。The thickness of the obtained molded body was 1.8 mm, and traces of the glass fiber used as a reinforcing material were observed to be raised on the resin layer on the surface. The surface shape was measured under the same conditions as in Example 1 and is shown in FIG.
(発明の効果)
本発明によれば、剛性、および表面平滑性のきわめて良
好な成形体を容易に得ることが出来る。(Effects of the Invention) According to the present invention, a molded article having extremely good rigidity and surface smoothness can be easily obtained.
図1は、本発明を用いた成形体の一例であり、図2は、
本発明の実施例1により得られた成形体の表面形状、図
3は比較例1で得られた成形体の表面形状を示す。
1 :弾性体FIG. 1 shows an example of a molded article using the present invention, and FIG.
FIG. 3 shows the surface shape of the molded product obtained in Example 1 of the present invention, and FIG. 3 shows the surface shape of the molded product obtained in Comparative Example 1. 1: Elastic body
Claims (2)
にある弾性体を核材とし、その周囲に配置された繊維強
化材、および該繊維強化材に含浸されたマトリックス樹
脂から構成されることを特徴とする繊維強化樹脂成形体
。(1) It is characterized by being composed of an elastic body in a compressed state that is not substantially impregnated with matrix resin as a core material, a fiber reinforced material arranged around the core material, and a matrix resin impregnated in the fiber reinforced material. Fiber-reinforced resin molded body.
およびその周囲に該弾性体に接するように配置された繊
維強化材を型の中に載置し、型を閉じた後、該弾性体を
圧縮したままマトリックス樹脂を注入して加熱硬化する
ことを特徴とする繊維強化樹脂成形体の製造方法。(2) an elastic body that is not substantially impregnated with matrix resin;
A fiber reinforced material placed around the elastic body in contact with the elastic body is placed in a mold, and after the mold is closed, a matrix resin is injected and heated to harden the elastic body while keeping it compressed. A method for producing a characteristic fiber-reinforced resin molded article.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1327662A JPH03187726A (en) | 1989-12-18 | 1989-12-18 | Fiber-reinforced resin molded item and preparation thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1327662A JPH03187726A (en) | 1989-12-18 | 1989-12-18 | Fiber-reinforced resin molded item and preparation thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03187726A true JPH03187726A (en) | 1991-08-15 |
Family
ID=18201567
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1327662A Pending JPH03187726A (en) | 1989-12-18 | 1989-12-18 | Fiber-reinforced resin molded item and preparation thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03187726A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7942637B2 (en) | 2008-12-11 | 2011-05-17 | General Electric Company | Sparcap for wind turbine rotor blade and method of fabricating wind turbine rotor blade |
-
1989
- 1989-12-18 JP JP1327662A patent/JPH03187726A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7942637B2 (en) | 2008-12-11 | 2011-05-17 | General Electric Company | Sparcap for wind turbine rotor blade and method of fabricating wind turbine rotor blade |
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