JPH0247326B2 - - Google Patents
Info
- Publication number
- JPH0247326B2 JPH0247326B2 JP58109824A JP10982483A JPH0247326B2 JP H0247326 B2 JPH0247326 B2 JP H0247326B2 JP 58109824 A JP58109824 A JP 58109824A JP 10982483 A JP10982483 A JP 10982483A JP H0247326 B2 JPH0247326 B2 JP H0247326B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- core
- cavity
- particulate matter
- molding
- 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.)
- Expired - Lifetime
Links
- 229920005989 resin Polymers 0.000 claims description 18
- 239000011347 resin Substances 0.000 claims description 18
- 239000013618 particulate matter Substances 0.000 claims description 15
- 238000000465 moulding Methods 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- 238000007789 sealing Methods 0.000 claims description 2
- 238000001179 sorption measurement Methods 0.000 claims 1
- 239000002245 particle Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000011236 particulate material Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Moulds For Moulding Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
本発明はアンダーカツト部を有する成形品を常
温硬化性樹脂により成形する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of molding a molded article having an undercut portion using a cold-setting resin.
従来、アンダーカツト部を有する成形品を常温
硬化性樹脂により成形するには、型抜きの理由か
ら、複数個に分割された金型や樹脂型あるいはス
ライドコアを用いて行つており、そのため、金型
や樹脂型は高価なものとなり、しかも成形操作が
複雑になる上に成形品にばかり発生しやすかつ
た。さらに、成形品のアンダーカツト部内に着色
塗装を施すことがきわめて困難であるなどの問題
があつた。 Conventionally, molded products with undercuts have been molded using room-temperature curable resins for reasons of mold cutting, using a mold divided into multiple parts, a resin mold, or a slide core. Molds and resin molds were expensive, molding operations were complicated, and molding was more likely to occur. Furthermore, there were other problems such as it was extremely difficult to apply colored coating to the inside of the undercut portion of the molded product.
本発明は上記の問題を解消するためになされた
もので、以下、本発明の一実施例について図面に
基づき詳細に説明する。 The present invention has been made to solve the above problems, and one embodiment of the present invention will be described in detail below with reference to the drawings.
第1図に示すように、中空室1,2内を吸引減
圧して木型あるいは石ころ型の垂直割マスター型
3のベントホール5,5を介してコアキヤビテイ
4の表面に吸引作用を働かせ、コアキヤビテイ4
の開口6があるマスター型3上面に、シータ7に
より加熱されて伸長性が増した成形フイルム8を
載せる。これにより、第2図に示すように成形フ
イルム8は吸引伸長されながらコアキヤビテイ4
の表面に吸着される。そこで第3図に示すよう
に、成形フイルム8が吸着されたコアキヤビテイ
4内に吸引管9を挿入するとともに平均粒径
100μの粒子状物質Mを充填し、続いて、マスタ
ー型3上面上および粒子状物質M上に密閉フイル
ム10を被せるとともにフイルム8,10同士を
融着接合あるいは接着テープで接合して開口6を
気密に閉鎖し、その後、粒子状物質Mが充填され
たコアキヤビテイ4内を吸引管9を介して吸引減
圧して粒子状物質Mを固化状態にし、もつてコア
型Cを成形する。 As shown in FIG. 1, the pressure inside the hollow chambers 1 and 2 is reduced by suction, and a suction action is applied to the surface of the core cavity 4 through the vent holes 5 and 5 of the vertically split master mold 3 in the form of a wooden or stone type. 4
A molded film 8 heated by a sheeter 7 to have increased extensibility is placed on the upper surface of the master mold 3 having an opening 6. As a result, as shown in FIG.
is adsorbed to the surface of Therefore, as shown in FIG. 3, a suction tube 9 is inserted into the core cavity 4 where the formed film 8 is adsorbed, and the average particle diameter is
After filling the particulate matter M with a thickness of 100μ, a sealing film 10 is placed over the upper surface of the master mold 3 and the particulate matter M, and the openings 6 are formed by joining the films 8 and 10 together with fusion bonding or adhesive tape. The core cavity 4 filled with the particulate matter M is then vacuumed and depressurized through the suction pipe 9 to solidify the particulate matter M, thereby molding the core mold C.
次いで、第4図に示すようにマスター型3を左
右に開くと、フイルム8,10内の粒子状物質M
が所定形状に固化されて成るコア型Cを取り出す
ことができる。こうして得たコア型Cを第5図に
示すように成形用型11内にセツトして成形用型
11とコア型Cとで製品キヤビテイ12を画成
し、注入口13からこの製品キヤビテイ12内に
液状の常温硬化性樹脂を流し込み製品キヤビテイ
12内を常温硬化性樹脂で充満させる。常温硬化
性樹脂の硬化後、吸引管9による吸引を停止して
コア型Cの固化状態を崩壊させ、粒子状物質Mを
成形用型11から排出させると、アンダーカツト
部を有する成形品を得ることができる。 Next, as shown in FIG. 4, when the master mold 3 is opened left and right, the particulate matter M in the films 8 and 10 is removed.
A core mold C formed by solidifying into a predetermined shape can be taken out. The core mold C thus obtained is set in a molding mold 11 as shown in FIG. 5, and a product cavity 12 is defined by the molding mold 11 and the core mold C. A liquid room temperature curable resin is poured into the product cavity 12 to fill the product cavity 12 with the room temperature curable resin. After the room temperature curable resin is cured, the suction by the suction pipe 9 is stopped to collapse the solidified state of the core mold C, and the particulate matter M is discharged from the mold 11 to obtain a molded product having an undercut portion. be able to.
なお、コアキヤビテイが深く1枚のフイルムで
絞ることができない場合には、コア型は、前述し
たと同様の方法で作つた複数個のコア型C1,C2
を貼り合わせ、あるいは接着テープにより接合し
て一体化させる方法により製作したものでよい
(第6図参照)。 In addition, if the core cavity is deep and cannot be squeezed with a single film, the core mold can be made of multiple core molds C 1 and C 2 made in the same manner as described above.
They may be manufactured by bonding them together or by joining them with adhesive tape to integrate them (see Fig. 6).
前述した実施例で使用されるフイルム8,10
の材料としては、ポリエチレン、ポリプロピレ
ン、ポリスチレン、塩化ビニール、塩化ビニリデ
ン、ポリアミド、ポリカーボネート、アイオノマ
ー、エチレン−酢酸ビニール共重合体、ポリオレ
フインブロツク重合体等の熱可塑性樹脂、合成ゴ
ムおよび天然ゴムなどがある。これらの材料に顔
料、染料、金属はくなどの着色剤を含有あるいは
塗装したもの、紫外線吸収剤を含有あるいは塗装
したものをフイルム8,10として用いることに
よつて成形品に着色することができる。フイルム
8,10は粒子状物質Mの排出後、成形品に装着
した状態で取り出されるが、成形品にフイルム
8,10が不要な場合には、フイルム8,10を
剥離できるように常温硬化性樹脂の種類とフイル
ムの材質について考慮したり、フイルム8,10
の表面に予め離型剤を塗布しなければならない。
一方、成形品に着色するため、上記のように特別
に処理したフイルム8,10を用いてこのフイル
ム8,10を成形品に装着させた状態にする必要
がある場合には、余分な部位のフイルム8,10
を切断除去すればよいが、成形品とフイルム8,
10との接着性が乏しいときには、フイルム8,
10に予め接着剤を塗布するなどの処理が必要で
ある。また、粒子状物質Mとしては、金属粉、ガ
ラス粉、砂、その他の無機化合物粉などの無機系
粒子、および木粉、プラスチツク粉などの有機系
粒子がある。そして、この粒子状物質の必要な性
質は、充填性が良いことであり、さらに、常温硬
化性樹脂が硬化時に発熱したり、成形時にある程
度加熱する必要があるときには、これらの温度に
十分耐え得るように耐熱性を有することである。
また、粒子状物質の粒径は10μ〜3mm程度でよい
が、成形品表面の平滑度が粒径の影響を受けるた
め注意を要する。粒径が小さければ成形品表面の
平滑度や細かな凹凸模様の転写性が良好になる
が、粒子状物質の取扱いが困難になりかつ発塵し
て環境を悪くする。一方、粗い粒子では逆の現象
が生じることになり、一般には粒径50〜600μ程
度のものがよい。 Films 8 and 10 used in the above embodiments
Examples of the material include thermoplastic resins such as polyethylene, polypropylene, polystyrene, vinyl chloride, vinylidene chloride, polyamide, polycarbonate, ionomer, ethylene-vinyl acetate copolymer, polyolefin block polymer, synthetic rubber, and natural rubber. Molded products can be colored by using these materials as films 8 and 10 containing or coating coloring agents such as pigments, dyes, and metal foils, or containing or coating ultraviolet absorbers. . After the particulate matter M has been discharged, the films 8 and 10 are taken out while being attached to the molded product, but if the films 8 and 10 are not required for the molded product, they are cured at room temperature so that they can be peeled off. Consider the type of resin and film material, and
A mold release agent must be applied to the surface of the mold in advance.
On the other hand, if it is necessary to attach the specially treated films 8, 10 to the molded product in order to color the molded product, it is necessary to attach the films 8, 10 to the molded product in order to color the molded product. Film 8,10
It is sufficient to cut and remove the molded product and film 8,
When the adhesion with film 10 is poor, film 8,
10 requires treatment such as applying adhesive in advance. The particulate matter M includes inorganic particles such as metal powder, glass powder, sand, and other inorganic compound powders, and organic particles such as wood powder and plastic powder. The necessary properties of this particulate material are that it has good filling properties, and furthermore, when room-temperature curing resins generate heat during curing or require a certain degree of heating during molding, it must be able to withstand these temperatures sufficiently. It has heat resistance.
Further, the particle size of the particulate material may be about 10 μm to 3 mm, but care must be taken because the smoothness of the surface of the molded product is affected by the particle size. If the particle size is small, the smoothness of the surface of the molded product and the transferability of fine uneven patterns will be improved, but the particulate matter will be difficult to handle and will generate dust, which will worsen the environment. On the other hand, the opposite phenomenon will occur with coarse particles, and generally particles with a diameter of about 50 to 600 μm are preferable.
なお、常温硬化性樹脂としては、ポリウレタ
ン、ポリエステル、アクリル樹脂、エポキシ樹
脂、ポリアミド、フラン樹脂、シリコン樹脂、あ
るいはこれらの変性樹脂などがある。 Note that the room temperature curable resin includes polyurethane, polyester, acrylic resin, epoxy resin, polyamide, furan resin, silicone resin, and modified resins thereof.
以上の説明から明らかなように本発明は、粒子
状物質をフイルムにより気密に包囲するとともに
このフイルム内を吸引減圧して粒子状物質を固化
させることによりコア型を成形し、該コア型を成
形用型内にセツトして製品キヤビテイを画成し、
該製品キヤビテイ内に液状の常温硬化性樹脂を充
満し、樹脂の硬化後、吸引管の吸引作用を停止し
て粒子状物質を排出させるようにしたから、複数
個に分割された高価な金型や樹脂型あるいはスラ
イドコアを用いなくとも、安価な木型や石こう型
を用いてアンダーカツト部を有する成形品を常温
硬化性樹脂により適確に成形できしかも、着色剤
を含有・塗装したフイルムを用いることにより成
形品に容易に着色でき、その上、コア型に割り面
がないので成形品にはばりが生じないなどの優れ
た効果を奏する。 As is clear from the above description, the present invention molds a core mold by airtightly surrounding particulate matter with a film and solidifying the particulate matter by suctioning and reducing the pressure inside the film. Set in the mold to define the product cavity,
The product cavity is filled with liquid room-temperature curing resin, and after the resin hardens, the suction action of the suction tube is stopped to discharge particulate matter, which eliminates the need for expensive molds that are divided into multiple pieces. It is possible to accurately mold a molded product with an undercut using an inexpensive wooden mold or plaster mold using a cold-curing resin without using a resin mold or a slide core. By using it, molded products can be easily colored, and since there is no split surface in the core mold, excellent effects such as no burrs are produced on the molded products are achieved.
第1図〜第5図は本発明の一つの実施例の工程
を示す縦断面図、第6図は本発明に使用するコア
型の他の実施例を示す縦断面図である。
4:コアキヤビテイ、6:開口、8:フイル
ム、9:吸引管、10:フイルム、11:成型用
型、12:製品キヤビテイ。
1 to 5 are longitudinal cross-sectional views showing the steps of one embodiment of the present invention, and FIG. 6 is a longitudinal cross-sectional view showing another embodiment of the core mold used in the present invention. 4: Core cavity, 6: Opening, 8: Film, 9: Suction tube, 10: Film, 11: Molding mold, 12: Product cavity.
Claims (1)
イルムを吸着させるとともに前記コアキヤビテイ
と連通する開口から当該コアキヤビテイ内に吸引
管を挿入するとともに粒子状物質を装入充填し、
続いて前記開口を密閉フイルムで気密に閉鎖し、
前記吸引管をもつて両フイルムで包囲する内部を
吸引減圧して粒子状物質を固化状態にしもつてコ
ア型を形成し、前記成形フイルムのコアキヤビテ
イ表面への吸着状態を解いたのち離型し、該コア
型を成形用型内にセツトして成形用型とコア型と
で製品キヤビテイを画成し、該製品キヤビテイ内
に液状の常温硬化性樹脂を充満させ、該常温硬化
性樹脂の硬化後、前記吸引管による吸引を停止し
て前記コア型を崩壊させるとともに粒子状物質を
前記成形用型から排出させることを特徴とする常
温硬化性樹脂の成形方法。1 Adsorb a molded film onto the surface of the core cavity of the master mold, insert a suction pipe into the core cavity from an opening communicating with the core cavity, and charge particulate matter;
Subsequently, the opening is hermetically closed with a sealing film,
Using the suction tube, the inside surrounded by both films is sucked and depressurized to solidify the particulate matter to form a core mold, and after releasing the adsorption state of the molded film to the surface of the core cavity, the mold is released; The core mold is set in a molding mold to define a product cavity between the molding mold and the core mold, the product cavity is filled with a liquid room temperature curable resin, and after the room temperature curable resin is cured. . A method for molding a room-temperature curable resin, characterized in that suction by the suction tube is stopped to collapse the core mold and to discharge particulate matter from the mold.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10982483A JPS60909A (en) | 1983-06-17 | 1983-06-17 | Molding method of cold-setting resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10982483A JPS60909A (en) | 1983-06-17 | 1983-06-17 | Molding method of cold-setting resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60909A JPS60909A (en) | 1985-01-07 |
JPH0247326B2 true JPH0247326B2 (en) | 1990-10-19 |
Family
ID=14520136
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10982483A Granted JPS60909A (en) | 1983-06-17 | 1983-06-17 | Molding method of cold-setting resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60909A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62172019U (en) * | 1986-04-21 | 1987-10-31 | ||
DE3934153A1 (en) | 1989-10-12 | 1991-04-18 | Johnson & Johnson Gmbh | TAMPON, ESPECIALLY FOR WOMEN'S HYGIENE, AND METHOD AND DEVICE FOR PRODUCING THE SAME |
JP4721251B2 (en) * | 2001-09-03 | 2011-07-13 | 富士重工業株式会社 | Manufacturing method of composite reinforcing plate |
DE102006031325B4 (en) | 2006-07-06 | 2010-07-01 | Airbus Deutschland Gmbh | Method for producing a fiber composite component for aerospace applications |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4851060A (en) * | 1971-10-29 | 1973-07-18 | ||
JPS5983609A (en) * | 1982-11-04 | 1984-05-15 | Aisin Seiki Co Ltd | Preparation of molded hollow resin product |
-
1983
- 1983-06-17 JP JP10982483A patent/JPS60909A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4851060A (en) * | 1971-10-29 | 1973-07-18 | ||
JPS5983609A (en) * | 1982-11-04 | 1984-05-15 | Aisin Seiki Co Ltd | Preparation of molded hollow resin product |
Also Published As
Publication number | Publication date |
---|---|
JPS60909A (en) | 1985-01-07 |
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