JPH01195027A - Method for molding synthetic resin - Google Patents
Method for molding synthetic resinInfo
- Publication number
- JPH01195027A JPH01195027A JP63018594A JP1859488A JPH01195027A JP H01195027 A JPH01195027 A JP H01195027A JP 63018594 A JP63018594 A JP 63018594A JP 1859488 A JP1859488 A JP 1859488A JP H01195027 A JPH01195027 A JP H01195027A
- Authority
- JP
- Japan
- Prior art keywords
- fillers
- matrix
- molded
- resin solution
- molded product
- 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
- 238000000034 method Methods 0.000 title claims abstract description 20
- 238000000465 moulding Methods 0.000 title claims abstract description 17
- 229920003002 synthetic resin Polymers 0.000 title claims description 7
- 239000000057 synthetic resin Substances 0.000 title claims description 7
- 229920005989 resin Polymers 0.000 claims abstract description 30
- 239000011347 resin Substances 0.000 claims abstract description 30
- 239000000945 filler Substances 0.000 claims abstract description 27
- 239000011159 matrix material Substances 0.000 claims abstract description 19
- 239000007788 liquid Substances 0.000 claims description 12
- 238000011074 autoclave method Methods 0.000 abstract description 2
- 230000006835 compression Effects 0.000 abstract description 2
- 238000007906 compression Methods 0.000 abstract description 2
- 238000005470 impregnation Methods 0.000 abstract description 2
- 239000002928 artificial marble Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 5
- 239000000178 monomer Substances 0.000 description 4
- 230000008602 contraction Effects 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000003980 solgel method Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- LFVLUOAHQIVABZ-UHFFFAOYSA-N Iodofenphos Chemical compound COP(=S)(OC)OC1=CC(Cl)=C(I)C=C1Cl LFVLUOAHQIVABZ-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 241000283220 Odobenus rosmarus Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- UGGQKDBXXFIWJD-UHFFFAOYSA-N calcium;dihydroxy(oxo)silane;hydrate Chemical compound O.[Ca].O[Si](O)=O UGGQKDBXXFIWJD-UHFFFAOYSA-N 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Landscapes
- Moulding By Coating Moulds (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
この発明は、キッチンカウンターなどの材料として好適
に用いられる合成樹脂の成形法に関し、充填材を成形し
て充填材同士が結合した状態の成形品を形成したのち、
マトリックス樹脂液を含浸、硬化させることにより、特
に耐熱性の良好な成形体が得られる」;うにしたもので
ある。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method of molding a synthetic resin that is suitably used as a material for kitchen counters, etc. The present invention relates to a method of molding a synthetic resin that is suitably used as a material for kitchen counters, etc. After forming the product,
By impregnating and curing the matrix resin liquid, a molded article with particularly good heat resistance can be obtained.
[従来の技術]
従来より、キッチンカウンターなどとして用いられる合
成樹脂の成形体の一つに、第2図に示したような、いわ
ゆる人造大理石と呼ばれるものがある。そしてこのよう
な人造大理石の製造に際しては、水酸化アルミニウムな
どの充填+A’ 1をアクリル樹脂などのマトリックス
樹脂2と混合してなる混合物を、成形型を用いて所定の
形状に成形、硬化させる方法が広く用いられていた。[Prior Art] One of the synthetic resin moldings conventionally used for kitchen counters and the like is so-called artificial marble, as shown in FIG. When manufacturing such artificial marble, there is a method in which a mixture of filling material such as aluminum hydroxide + A' 1 is mixed with matrix resin 2 such as acrylic resin is molded into a predetermined shape using a mold and hardened. was widely used.
[発明が解決しようとする課題]
とごろが、このような方法によって製造される人造大理
石にあっては、第2図に示したように各々の充填材lが
マトリックス樹脂2中に分散された状態となっており、
各充填材1・間にはなんら結合力は存在していない。こ
のため、この人造大理石が加熱条件下に置かれた際?こ
は、7トリツクス樹脂2の熱膨張ににる流動が自由に進
行するため、熱応力が増大し、その結果割れやひびが入
るなどの不都合が生じる。また、このような人造大理石
はその製造時に成形型を用いて成形するので、成形時に
成形型による残留歪が生じる場合が多々あり、この残留
歪が大きい場合には、加熱された際に、その部分が熱収
縮して割れが生しるなどの不都合が起こる。すなわち、
耐熱性不良という問題かあった。[Problems to be Solved by the Invention] In the artificial marble manufactured by this method, each filler l is dispersed in the matrix resin 2 as shown in FIG. The condition is
There is no bonding force between each filler 1. Because of this, when this artificial marble is placed under heating conditions? This is because the flow due to the thermal expansion of the 7trix resin 2 proceeds freely, increasing thermal stress, resulting in problems such as cracks and cracks. In addition, since such artificial marble is molded using a mold during its manufacture, residual strain is often caused by the mold during molding, and if this residual strain is large, it may be damaged when heated. Inconveniences such as parts shrinking due to heat and cracks occur. That is,
There was a problem with poor heat resistance.
そこでこの発明は」二連の課題を解決し、熱膨張率およ
び熱収縮率の小さな、すなわち耐熱性の良好な成形体が
得られろ合成樹脂の成形法を提供することを目的として
いる。SUMMARY OF THE INVENTION It is an object of the present invention to solve the two problems and provide a method for molding a synthetic resin, which yields a molded article with a small coefficient of thermal expansion and a small coefficient of thermal contraction, that is, a molded article with good heat resistance.
[課題を解決するための手段]
この発明は、充填十Aを成形して充填剤同士が結合した
状態の成形品を形成したのち、マトリックスとなる樹脂
液を含浸、硬化させることをその解決手段とする。[Means for Solving the Problems] The present invention has a method of solving the problem by molding the filled material to form a molded product in which the fillers are bonded to each other, and then impregnating and curing the resin liquid that becomes the matrix. shall be.
以下、この発明の詳細な説明する。The present invention will be described in detail below.
この発明において使用される充填材としては、繊維状、
フレーク状なとの形状を有するもので、アスペクト比が
3以」−1より好ましくは5以」二と大きならのが好適
に使用される。具体的には例えばウオラストナイト、ヂ
タン酸カリウム、石こう繊維、ゾノトライト、斜状合成
マグネシウム系フィラー(MOS)、スラグ繊維(PM
F)、セピオライト、マイカ、タルク、カラス繊維など
の無機フィラーなどがある。The fillers used in this invention include fibrous,
It has a flaky shape and has an aspect ratio of 3"-1 or more, preferably 5 or more"2, and is preferably used. Specifically, for example, wollastonite, potassium ditanate, gypsum fiber, xonotlite, oblique synthetic magnesium filler (MOS), slag fiber (PM
F), inorganic fillers such as sepiolite, mica, talc, and glass fiber.
これらの充填材を、まず所望の形状に予備成形する。予
備成形法には、紙すき法、圧密法、プレス法などの方法
か利用されろ。そして、得られろ予備成形品のかさ密度
が01〜1 、 7 g/ cm″程度、またその空隙
率が96〜40%程度となるように成形するのが好まし
い。ここで、」1記充填祠にはアスペクト比の比較的大
きなものを用いているので、成形時に物理的な結合ある
いは絡まり合いが生じているが、これらの結合点あるい
は接合点をより強固に結合させるために、種々の化学的
結合手段を用いてもよい。ごの手段としては、ソリ力、
金属等のアルコキン)・なとをゾルゲル法などによって
含浸、固化させる方法や、または加熱して焼成する方法
などが利用されろ。またさらに、この充填材の予備成形
時に(J、必要に応じて適宜の着色剤を混入させて同情
成形することにより、美観を高めることもできる。この
着色剤には、染顔料を溶剤に溶解したもの、あるいはこ
れに少量の樹脂分、例えばポリウレタン系樹脂等を溶解
させたものなどが好適に使用される。These fillers are first preformed into the desired shape. For the preforming method, methods such as paper making method, consolidation method, pressing method, etc. may be used. Then, it is preferable to mold the obtained preformed product so that its bulk density is about 01 to 1.7 g/cm'' and its porosity is about 96 to 40%. Because shrines are made with relatively large aspect ratios, physical bonds or entanglements occur during molding, but in order to make these bonding points or bonding points more firmly bonded, various chemical treatments have been applied. You may also use a specific linking means. As a means of control, sled force,
Methods such as impregnating and solidifying metals (alcoquines, etc.) using a sol-gel method, or methods of heating and firing may be used. Furthermore, it is possible to improve the aesthetic appearance by mixing an appropriate coloring agent as necessary during preforming of this filler and molding it.This coloring agent includes dyes and pigments dissolved in a solvent. or a small amount of resin, such as a polyurethane resin, dissolved therein is preferably used.
次いで、この充填材からなる予備成形品にマトリ7クス
となる樹脂液を含浸、硬化させる。このマトリックス樹
脂液としては、上記予備成形品の微細な網目状の空隙の
中に浸透しやすいものでなくてはならず、低粘度のムの
で、未硬化時の状態が比較的低分子亀のらのが好ましい
。例えば熱硬化性樹脂初期縮合物、熱可塑性樹脂モノマ
ーまたはその部分重合物などて、具体的にはメヂルメタ
クリレート(MMΔ)モノマーのような低粘度のもので
、熱により重合するタイプのものが好ましい。Next, the preformed product made of this filler is impregnated with a resin liquid that will become the matrix 7 and hardened. This matrix resin liquid must be able to easily penetrate into the fine mesh-like voids of the preformed product, and because it has a low viscosity, the uncured state is a relatively low-molecular weight resin. is preferred. For example, a thermosetting resin initial condensate, a thermoplastic resin monomer, or a partial polymer thereof, etc., specifically, a low viscosity material such as methyl methacrylate (MMΔ) monomer, which is preferably a type that can be polymerized by heat. .
またこのようなメタクリル樹脂系の他にも、不飽和ポリ
エステル樹脂系、ジアリルフタレート樹脂系、ケイ素樹
脂系、エボキン樹脂系、ポリウレタン樹脂系、モノマー
注形型ポリアミド樹脂系などの低粘度品を使用ずろこと
もてきる。また、このマトリックス樹脂液としてメタク
リル樹脂系、ポリエステル樹脂系などの透明なものを用
いれば、上記充填材の網目構造があたかも模様のように
透(Jて見え、趣のあろ成形体かiUられろ効果もある
。In addition to methacrylic resins, we also use low-viscosity products such as unsaturated polyester resins, diallyl phthalate resins, silicone resins, Evokin resins, polyurethane resins, and monomer-cast polyamide resins. It can also happen. In addition, if a transparent material such as methacrylic resin or polyester resin is used as the matrix resin liquid, the network structure of the filler will be visible as if it were a pattern, and the molded product will look different from the original. It's also effective.
またこの7トリツクス樹脂液の含浸け、オートクレーブ
法などによって実施ずろ。例えばオートクレーブ内にて
、」−記マトリックス樹脂液中に」−記予備成形品を浸
漬して含浸せしめたのち、必要に応じて非酸素雰囲気下
て、室温〜200°C1常圧〜2 M P a程度の加
熱加圧条件で含浸樹脂液を硬化uしめる。In addition, impregnation with this 7 Trix resin solution can be carried out by an autoclave method, etc. For example, in an autoclave, after immersing the preformed product in the matrix resin liquid to impregnate it, if necessary, in a non-oxygen atmosphere, at room temperature to 200°C, normal pressure to 2 MPa. The impregnating resin liquid is hardened under heating and pressurizing conditions of approximately 1.
このような方法によれば、得られろ成形体(J、第1図
に示したように充填1711 が化学的にあるいは物
理的に結合し合ってなる網目状構造の成形品中に」二記
マトリックス樹脂液2か含浸し、硬化してなるものであ
るので、熱膨張率の小さい充填材l ・粒子にJ二って
マトリックス樹脂2の膨張あるいは収縮等の動きか抑制
されるため、従来の人造大理石に比べて、その耐熱性が
著しく向」ニしたものとなる。また、成形時に成形型を
用いないので、型による残留歪が成形体3に残ることが
なく、加熱条件下に置かれても熱変形して割れたりひび
が入ったりするなどの不都合がない。また」二連のよう
な充填材l ・が結合し合ってなる網II状+14迅を
有しているため、強度的にも従来の人造大理石に優って
いる。According to such a method, a molded article (J) having a network structure in which the fillings 1711 are chemically or physically bonded to each other as shown in FIG. Since it is impregnated with the matrix resin liquid 2 and cured, it is a filler with a small coefficient of thermal expansion.The J2 particles suppress the movement of the matrix resin 2, such as expansion or contraction. Its heat resistance is significantly better than that of artificial marble.In addition, since no mold is used during molding, residual strain caused by the mold does not remain in the molded product 3, and it can be placed under heating conditions. There is no inconvenience such as breakage or cracking due to heat deformation even when the material is heated.Also, since it has a network shape made of two-part filler material bonded to each other, it has a high strength. It is also superior to traditional artificial marble.
[実施例]
(実施例I)
充填しとして繊維状のウォラス)・ナイトを用い、これ
を圧縮プレス法により厚さ10mmの高密度(10)の
板状の予備成形品を形成した。[Example] (Example I) Using fibrous walrus night as a filler, a high-density (10) plate-like preformed product with a thickness of 10 mm was formed by compression pressing.
この予備成形品を、メチルメタクリレート(MMΔ)モ
ノマー液と2重重%のアゾビスイソブヂロニトリル(Δ
IBN)との混合液中に浸漬し、オートクレーブ内’−
Q−700mmHgテ20分間含浸したのち、さらにオ
ートクレーブにて窒素雰囲気下、60°C,9,5at
mの加圧条件で硬化させた。This preform was mixed with methyl methacrylate (MMΔ) monomer liquid and 2% by weight of azobisisobutyronitrile (Δ
IBN) and placed in an autoclave.
After impregnating with Q-700mmHg for 20 minutes, further autoclave under nitrogen atmosphere at 60°C, 9.5at
It was cured under pressure conditions of m.
ここで、このMM△モノマーに対する上記充填材の割合
(」、37体積%てあった。Here, the ratio of the filler to the MMΔ monomer was 37% by volume.
(比較例)
アクリル樹脂ど、水酸化アルミニウム粉よりなる充填材
を38体積%混合してなる混合物を、板状の成形型に流
し込み、温度60℃の条件で加熱成形し、−1−記樹脂
を硬化させて、厚さ10mm0人造大理石を製造した。(Comparative example) A mixture of 38% by volume of a filler such as acrylic resin and aluminum hydroxide powder is poured into a plate-shaped mold and heat-molded at a temperature of 60°C to form the -1- resin. was cured to produce a 10 mm thick artificial marble.
以」二のようにして製造した実施例および比較例のそれ
ぞれの成形体を用いて、熱的機械的分析装置(T M
A )により熱膨張率を測定した。またさらに、」−記
実施例および比較例の成形体を230°Cに加熱した後
に再び常温に戻した時の膨張収縮率を、同様にTMAに
より測定した。これらの結果を合わせて第1表に示す。Using a thermomechanical analysis device (T M
A) The thermal expansion coefficient was measured. Furthermore, the expansion/shrinkage ratios of the molded bodies of Examples and Comparative Examples ``-'' were similarly measured by TMA when the molded bodies were heated to 230°C and then returned to room temperature. These results are shown in Table 1.
第 1 表
第1表から明らかなように、この発明の実施例の成形体
は、従来の人造大理石と同程度の量の充填材を含んでい
るにもかかわらず、熱膨張率か1 、 I x、I
0−5(1/’C)と、プラスチック材料としではフェ
ノール積層板以下の非常に小さな値を示している。また
、(230’C−常温)処理を施した後でも、実施例の
成形体にあっては収縮は起こら1゛、僅かな膨張が起こ
るだけであり、非常に良好な耐熱性を示している。Table 1 As is clear from Table 1, the molded articles of the embodiments of the present invention have a coefficient of thermal expansion of 1, I even though they contain the same amount of filler as conventional artificial marble. x, I
0-5 (1/'C), which is a very small value for a plastic material, lower than that of a phenol laminate. Furthermore, even after the treatment (230'C - room temperature), the molded articles of the examples did not shrink by 1゛ and only slightly expanded, indicating very good heat resistance. .
[発明の効果]
以」二説明したように、この発明の合成樹脂の成形法は
、充填材を成形して充填材同士が結合した状態の成形品
を形成したのち、マトリックスとなる樹脂液を含浸、硬
化させるものであるので、得られる成形体は、充填材が
化学的にあるいは物理的に結合し合ってなる網目状構造
の成形品中に上記マトリックス樹脂液が含浸し硬化して
なるものであるので、熱膨張率の小さい充填材粒子によ
ってマトリックス樹脂の膨張あるいは収縮等の動きが抑
制されるため、良好な耐熱性を有するものとなる。また
成形時に成形型を用いないため、型による残留歪が成形
体に残ることがなく、加熱条件下に置かれても熱変形し
て割れたりひびが入ったりするなとの不都合もない。ま
た上述のような構=8−
造を有しているため、強度的にも従来の人造大理石に優
っている。[Effects of the Invention] As explained below, the synthetic resin molding method of the present invention involves molding fillers to form a molded product in which the fillers are bonded together, and then adding a resin liquid to serve as a matrix. Since it is impregnated and cured, the resulting molded product is obtained by impregnating and curing the matrix resin liquid into a molded product with a network structure in which fillers are chemically or physically bonded to each other. Therefore, the filler particles having a small coefficient of thermal expansion suppress movements such as expansion or contraction of the matrix resin, resulting in good heat resistance. Furthermore, since a mold is not used during molding, residual strain caused by the mold will not remain in the molded product, and even if it is placed under heating conditions, there will be no inconvenience such as cracks or cracks due to thermal deformation. Furthermore, since it has the above-mentioned structure, it is superior to conventional artificial marble in terms of strength.
第1図は、この発明の方法により製造した成形体の一例
を模式的に示す概略断面図、
第2図(J、従来の人造大理石の一例を模式的に示す概
略断面図である。
I ・・充填材、 2 ・・マトリックス樹脂。FIG. 1 is a schematic sectional view schematically showing an example of a molded article produced by the method of the present invention, and FIG. 2 (J) is a schematic sectional view schematically showing an example of a conventional artificial marble. - Filler, 2... Matrix resin.
Claims (1)
形成したのち、 マトリックスとなる樹脂液を含浸、硬化させることを特
徴とする合成樹脂の成形法。[Claims] A method for molding a synthetic resin, which comprises molding fillers to form a molded product in which the fillers are bonded together, and then impregnating and curing the molded product with a resin liquid serving as a matrix.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63018594A JPH01195027A (en) | 1988-01-29 | 1988-01-29 | Method for molding synthetic resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63018594A JPH01195027A (en) | 1988-01-29 | 1988-01-29 | Method for molding synthetic resin |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01195027A true JPH01195027A (en) | 1989-08-04 |
Family
ID=11975965
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63018594A Pending JPH01195027A (en) | 1988-01-29 | 1988-01-29 | Method for molding synthetic resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01195027A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61121910A (en) * | 1984-11-19 | 1986-06-09 | Toyota Motor Corp | Manufacture of fiber reinforced resin molded product |
JPS61239933A (en) * | 1985-04-17 | 1986-10-25 | Tokai Carbon Co Ltd | Method for homogeneous formation of whisker preform |
JPS63152637A (en) * | 1986-12-16 | 1988-06-25 | Toray Ind Inc | Preform material for reinforcement of resin |
JPS649725A (en) * | 1987-07-03 | 1989-01-13 | Nissan Motor | Manufacture of curved surface preform for composite material |
-
1988
- 1988-01-29 JP JP63018594A patent/JPH01195027A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61121910A (en) * | 1984-11-19 | 1986-06-09 | Toyota Motor Corp | Manufacture of fiber reinforced resin molded product |
JPS61239933A (en) * | 1985-04-17 | 1986-10-25 | Tokai Carbon Co Ltd | Method for homogeneous formation of whisker preform |
JPS63152637A (en) * | 1986-12-16 | 1988-06-25 | Toray Ind Inc | Preform material for reinforcement of resin |
JPS649725A (en) * | 1987-07-03 | 1989-01-13 | Nissan Motor | Manufacture of curved surface preform for composite material |
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