JPH0510208B2 - - Google Patents

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Publication number
JPH0510208B2
JPH0510208B2 JP58140497A JP14049783A JPH0510208B2 JP H0510208 B2 JPH0510208 B2 JP H0510208B2 JP 58140497 A JP58140497 A JP 58140497A JP 14049783 A JP14049783 A JP 14049783A JP H0510208 B2 JPH0510208 B2 JP H0510208B2
Authority
JP
Japan
Prior art keywords
rubber
foaming
crosslinking
mold
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.)
Expired - Lifetime
Application number
JP58140497A
Other languages
Japanese (ja)
Other versions
JPS6032613A (en
Inventor
Hiroshi Kenbishi
Eishiro Noda
Yukinori Mitani
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.)
NAIGAI RUBBER IND
Original Assignee
NAIGAI RUBBER IND
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 NAIGAI RUBBER IND filed Critical NAIGAI RUBBER IND
Priority to JP58140497A priority Critical patent/JPS6032613A/en
Publication of JPS6032613A publication Critical patent/JPS6032613A/en
Publication of JPH0510208B2 publication Critical patent/JPH0510208B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

発明の技術分野 本発明は、各種フロート、パツキン、ガスケツ
ト、シール、クツシヨン類等の産業用品、履物底
材等の日常用品など全ゆる分野に有用なゴム発泡
成型品の製造方法に関するものである。 従来技術 ゴム発泡成型品は、重要な工業用ゴム製品であ
り、押出発泡製品、板状発泡製品、型物発泡製品
等として広い分野に使用されている。このうち、
型物発泡製品の独立気泡発泡体として、各種フロ
ート、パツキン、ガスケツト、シール、クツシヨ
ン類及び履物底材等に用いられる製品については
その要求性能が上がり、精密で複雑かつ異形のゴ
ム発泡製品の要請が高まりつつある。 これらのゴム発泡成型品としては、通常ゴムあ
るいはゴム及び合成樹脂の混合物に発泡剤を配合
したゴム系組成物(以下、発泡コンパウンドとい
う)の高圧2段発泡法によつて得られる独立気泡
発泡体が従来から主流を占めている。 この高圧2段発泡法による従来のゴム発泡成型
品の製法を概説すると、次のとおりである。 (1) 発泡コンパウンドを所要の精密なキヤビテイ
を有する1次金型に、キヤビテイ容量に対して
少なくとも100要領%以上仕込み、 (2) 高圧下(少なくともキヤビテイの投影面積当
り40Kg/cm2以上の圧力)で加熱し、発泡コンバ
ウンドに配合された発泡剤の分解ガスが大気中
に逸散しない程度に架橋を進め、発泡剤の分解
ガスを独立したバブルで存在させる。(この工
程を通常、1次架橋という。) (3) 次いで、1次架橋で得られた成型品を取り出
し、前記1次金型より大きなキヤビテイ容量を
有する製品金型(2次金型ともいう)に装入
し、 (4) 加圧下(製品金型が開かない程度の圧力があ
れば充分であり、1次架橋時より圧力は低くて
もよい)で加熱し、製品金型キヤビテイ内に充
分、発泡充満せしめ、同時に架橋を完結させ
る。(この工程を通常、2次架橋という。) (5) 発泡、架橋が完結した後、直ちに圧力を除い
て飛び出した発泡製品を取り出すか、あるいは
複雑かつ異形形状のために飛び出す際に発泡製
品が損なわれる場合には、加圧したまま冷却、
固化させてから金型を開き、製品を取り出す。 ところが、上記高圧2段発泡法には下記のよ
うな種々の問題点がある。 (a) 1次架橋、2次架橋の分離した2段階の製
造工程であり、成型金型が2種類必要とな
り、工数及び金型経費が大きくなる。 (b) 複雑かつ異形形状の発泡体、寸法精度が要
求される発泡体、あるいは異質組成の複合発
泡体等を得る場合は、製品形状、すなわち2
次金型に適切な形状及び発泡倍率をもたらす
ような1次金型のキヤビテイの設計が難かし
く、今後、高機能を要求される発泡製品の開
発に対応するこのが益々困難となる。 (c) 1次架橋工程においては、発泡ゴムパウン
ドをキヤビテイへ100%以上仕込む必要があ
るため、若干のはみ出しが発生し、材料ロス
が避けられない上、このはみ出し部を取り除
く仕上工程が必要となる。さらに、このはみ
出し部の気泡構造が仕上加工の際に破壊さ
れ、独立気泡発泡体としての品位が低下し、
製品の品質低下、バラツキ等の悪影響の要因
となる。 発明の目的 本発明は、以上のようなゴム発泡成型品の製造
において、従来の高圧2段発泡法の2工程でしか
も2種類の金型を使用する架橋発泡工程の欠点を
解消すべくなされたものであり、従来の高圧2段
発泡法で得られる独立気泡体と同等以上の物性を
有すると共に高品質の発泡成型品を、工数及び金
型費、材料等を低減でき、従つて低コストで生産
性よく製造できる省資源、省エネルギー型の製造
方法を提供することにある。 発明の構成 本発明は、製品金型のみを使用する直接成型法
であり、以下の2つの発明からなる。 まず、本発明に係る第1の発明は、製品金型に
予め必要な発泡倍率となるように、そのキヤビテ
イ容量以下の発泡コンパウンドを仕込み、その際
に生ずるキヤビテイの余剰の空間に外部から高圧
(約10Kg/cm2)の空気、窒素ガス等のガス体を導
入、充満させ、気密に保つて加圧状態に維持する
ことにより、加熱による発泡コンパウンドの過度
の先行発泡を抑制しながら架橋をある程度進行せ
しめ、次いで導入した高圧のガス体を解放し、さ
らに引続き加熱を続け、発泡・架橋を完結させる
方法である。 また、本発明に係る第2の発明は、基本的には
上記第1の発明の技術的手段を利用するものであ
るが、製品金型のキヤビテイの一部に少量の発泡
剤を配合した発泡コンパウンドを仕込み、キヤビ
テイの他部に上記コンパウンドより多量の発泡剤
を配合した発泡コンパウンドを仕込むなど、発泡
剤の配合量の異なる2種以上の発泡コンパウンド
を装入し、上記第1の発明と同様の方法により、
低密度発泡部分と堅固な比較的高密度の発泡部分
とを同時に一体成型する方法である。 発明の作用・効果及び態様 本発明の方法は、原理的には従来の高圧2段発
泡法と同様である。すわなち、架橋工程が1次架
橋、2次架橋の2段階で行なわれるという点では
同じである。しかし、その手段が従来の高圧2段
発泡法とは全く異なる。すなわち、従来の1次金
型の使用を省き、製品金型に発泡コンパウンドを
直接仕込み、高圧のガス体を導入、充満させるこ
とによつて、加熱による発泡コンパウンドの過度
の先行発泡を抑制しながら架橋をある程度進行せ
しめ、その後ガス体を解放し、引続き加熱を続け
て発泡・架橋を完結させるものであり、前記2段
階架橋を一連の一工程で行なうものである。 従つて、従来の高圧2段発泡法に比べて工数も
少なく、作業性、生産性を大巾に向上できる。ま
た、1次金型が不用であるため、金型経費が大巾
に低減できると共に、従来のように1次架橋工程
におけるはみ出し部が発生せず、1次架橋物の仕
上工程も不要となり、またはみ出し部分の気泡破
壊も防止できる。さらに、従来の高圧2段発泡法
では得ることが困難であつた複雑異形の独立気泡
発泡体が容易に製造できる。 なお、本発明の方法においては、ガス体による
加圧状態下で、加熱(1次加熱)による発泡コン
パウインドの過度の先行発泡を抑制しながら架橋
をある程度進行せしめ、その後ガス圧を解放して
引続き加熱(2次加熱)して発泡・架橋を完結さ
せるものであるから、1次加熱よりも2次加熱の
温度を高くした方が好ましい。 また、本発明に係る第2の発明は、発泡剤の配
合量の異なる2種以上の発泡コンパウンドを上記
方法によつて発泡・架橋させ、低発泡部分と高発
泡部分、従つて密度、硬さ、耐熱性等の諸物性の
異なる部分同志を同時に一体成型するものであ
る。 従来、例えば自動車キヤプレター用フロートに
は、要求性能上複雑な異形断面を持つものが多か
つた。しかも、軽量を要求される部分と強度を要
求される部分を同時に具有することが要求され、
このため可動金属性アームをフロート本体に強固
に取り付けたもの、あるいはマグネツトを埋設し
たもの等があつた。しかし、これらの金属部品は
1次架橋物に取付加工することになり、余分な取
付加工作業を要するという不具合があつた。一
方、上記強度を要求される部分を、発泡倍率が低
く、かつ硬度の高いゴム発泡体とし、発泡倍率の
高い軽量の部分と一体成型することが考えられ
る。しかし、これを従来の高圧2段発泡方で行な
つた場合、1次架橋物をそれぞれ別個に成型し、
これを冷却、固化して取り出した後、製品金型に
て2次架橋する必要がある。従つて、一旦冷却、
固化した一次架橋物を2次架橋しても低発泡倍率
部分と高発泡倍率部分との融合、密着が充分でな
く、その境界部分において折れ易く、また1次金
型として2個必要となり、製造工程数も増えて煩
雑化するなど、作業性、生産性やコストの点でも
問題がある。 ところが、本発明に係る第2の発明では、製品
金型1個を使用するのみで充分であり、しかも、
加熱しより1次架橋された1次架橋物は、冷却、
固化されることなく、そのまま2次架橋処理させ
るため、低発泡倍率部分と高発泡倍率部分との融
合・密着が充分に高いという効果が得られる。さ
らに、使用される金型は製品金型1個で済み、ま
た2段階架橋が一連の一工程で行なわれるため、
作業性や生産性に優れると共に、コストの点でも
有利である。 上記低発泡部分と高発泡部分の発泡コンパウン
ドは、発泡剤の配合量を変えた以外は同一の組成
物で構成することが、融合・密着性の点で最も好
ましいが、必ずしもこれに限らず、物性等の点で
大巾に異ならなり限り、異種の組成物から構成し
てもよい。 なお、以上の説明では、1個の製品に着目して
説明したが、製品金型に複数個のキヤビテイを設
けて、一工程で複数個の製品を同時に製造するこ
とも可能である。 原料ゴムとしては、ゴム発泡体製造に使用され
る全めるゴムが使用でき、例えば天然ゴムの外、
クロロプレンゴム、ニトリルゴム、SBR.ハイス
チレンゴム、ブチルゴム等の合成ゴムが単独でま
たは混合して使用され、さらにゴムと合成樹脂と
の共重合体あるいはブレンドポリマー等、各種原
料ゴムが使用できる。また、原料ゴムに配合され
る合成樹脂としては、フエノール樹脂、PVC、
スチレン等各種樹脂が知られている。また、発泡
剤としても、従来周知の無機発泡剤、有機発泡剤
が使用できる。 実施例 以下に実施例を示して、本発明を具体的に説明
する。なお、部数は重量部を示す。 実施例 1 本実施例においては、自動車燃料計用フロート
の例を示す。 発泡コンパウンドの組成: NBR 80部 PVC 20部 フエノール樹脂 60部 カーボンブラツク 30部 ZnO 5部 ステアリン酸 1部 加硫促進剤(DM1.5部 CZ0.5部) 2部 発泡剤(DPT) 6部 尿素系発泡助剤 2部 硫黄 30部 上記組成の配合物を混練して、圧延あるいは押
出してスラブ状とし、所要の形状、重量で製品金
型のキヤビテイ容量以下の容量に裁断、秤量して
金型に仕込む。例えば、第1図(縦断面図)及び
第2図(パーテイング面の平面図)に示すように
平型(縦:5cm、横:8cm、厚さ:1cmの直方体
キヤビテイ)で、密度0.25g/cm3の燃料計用フロ
ートを得るためには、40cm3の製品金型キヤビテイ
1に10gの発泡コンパウンド2を仕込めばよい。
割型3のキヤピテイ1の周囲には、キヤピテイ空
間の気密が保たれるように、パーテイング面にパ
ツキン溝6が設けられて該溝6にゴム製パツキン
4を嵌め込まれている。導入管5から高圧空気
(9〜9.8Kg/cm3)を圧入しながら、加圧プレスで
型締した状態で加熱する。 加熱は、約130℃(蒸気圧2Kg/cm3)で18分間
行なわれ、次いで高圧景気を解除し、引続き加圧
プレスを型締した状態で温度を約165℃(蒸気圧
6.5Kg/cm3)に上昇させ、30分間加熱し、発泡及
び架橋を完結させる。 その後、型締を保持したまま、加圧プレスの蒸
気を冷却水に切替えて10分間冷却し、製品を固化
させてから加圧プレス及び金型を開き、製品を取
り出す。 実施例 2 本実施例においては、自動車キヤプレター用フ
ロートの例を示す。 実施例1と同様の発泡コンパウンドを第3図に
示すいようなロツド状21a,21bで押し出
し、所要の長さ、重量に裁断、秤量し、第4図
(縦断面図)及び第5図(パーテイング面の平面
図)に示す金型に、フローエート本体部21aと
アーム部21bとして所要のキヤビテイ容量以下
に仕込む。 上記製品金型においても、前記実施例1で用い
た金型と同様に、キヤピテイ11の周囲には、パ
ーテイング面にパツキン溝61が設けられて、該
溝61にゴム製パツキン41が嵌め込まれる。加
圧プレスで型締めし、導入管51からN2ガス
(9.8Kg/cm3)を導入しながら、約130℃(蒸気圧
2Kg/cm3)で30分間加熱し、次いでN2ガスを解
放し、引続き型締を保持したまま、加圧プレス温
度を約170℃(蒸気圧7Kg/cm3)に昇温し、30分
間加熱を続け、発泡、架橋を完結させる。 その後、加圧プレスの蒸気を冷却水に切替え、
15分間水冷し、製品を固化させてから加圧プレス
を解除し、金型を開いて製品を取出す。 フロート本体にアーム部が強固に融合密着した
製品が同時成型できた。 実施例 3 本実施例では、複雑な模様を底面に有する覆物
底の実施例を示す。 発泡コンパウンドの組成: NR 100部* Nipol−2007 30部 ZnO 5部 ステアリン酸 1部 促進剤(DM) 0.6部 炭酸マグネシウム 50部 炭酸カルシウム 50部 プロセス油 15部 硫 黄 3部 発泡剤(DPT) 5部 尿素系発泡助剤 5部 *)スチレン(85%)−ブタジエン(15%)共
重合体、日本ゼオン株式会社製 上記組成の配合物を混練、圧延し、スラブ状2
2とし、第6図(縦断面図)及び第7図(パーテ
イング面の平面図)に示すように、所要のキヤビ
テイ容量以下に仕込み、キヤビテイ12の周囲の
パーテイング面に設けたパツキン溝62に気密用
ゴム製パツキン42を嵌め込み、加圧プレスで型
締めし、導入管52からN2ガス(9.8Kg/cm2)を
圧入しながら、約125℃(蒸気圧1.4Kg/cm2)で10
分間加熱し、次いでN2ガスを解除し、引続き型
締を保持したまま150℃(蒸気圧4Kg/cm2)で10
分間加熱し、発泡、架橋を完結させ、加圧プレス
を解除し、金型を開いて製品を取出す。 上記実施例1〜3で得られた発泡体の物性を下
記第1表及び第2表に示す。
TECHNICAL FIELD OF THE INVENTION The present invention relates to a method for manufacturing rubber foam molded products useful in all fields, including industrial products such as various floats, packings, gaskets, seals, and cushions, and everyday products such as footwear soles. BACKGROUND OF THE INVENTION Rubber foam molded products are important industrial rubber products and are used in a wide range of fields, such as extruded foam products, plate-shaped foam products, molded foam products, and the like. this house,
The required performance of closed-cell foam products used in various floats, packing, gaskets, seals, cushions, footwear sole materials, etc. is increasing, and the demand for precise, complex, and irregularly shaped rubber foam products is increasing. is increasing. These rubber foam molded products are usually closed-cell foams obtained by a high-pressure two-stage foaming method of a rubber composition (hereinafter referred to as a foaming compound) in which a foaming agent is blended with rubber or a mixture of rubber and synthetic resin. has traditionally been the mainstream. An overview of the conventional method for manufacturing rubber foam molded products using this high-pressure two-stage foaming method is as follows. (1) Fill a primary mold with the required precision cavity with the foaming compound by at least 100% of the cavity capacity, (2) Under high pressure (at least 40 kg/cm 2 or more per projected area of the cavity) ) to promote crosslinking to such an extent that the decomposed gas of the blowing agent blended in the foaming compound does not escape into the atmosphere, allowing the decomposed gas of the blowing agent to exist in independent bubbles. (This process is usually called primary crosslinking.) (3) Next, the molded product obtained by primary crosslinking is taken out and molded into a product mold (also called secondary mold) having a cavity capacity larger than that of the primary mold. ), and (4) heat under pressure (it is sufficient to have enough pressure to prevent the product mold from opening; the pressure may be lower than during the primary crosslinking), and then heat it in the product mold cavity. Complete foaming and complete crosslinking at the same time. (This process is usually referred to as secondary crosslinking.) (5) After foaming and crosslinking are completed, immediately remove the pressure and take out the foamed product, or remove the foamed product due to its complex and irregular shape. If it is damaged, cool it under pressure,
After solidifying, open the mold and take out the product. However, the above-mentioned high-pressure two-stage foaming method has various problems as described below. (a) It is a two-step manufacturing process in which primary crosslinking and secondary crosslinking are separated, and two types of molds are required, increasing the number of man-hours and mold costs. (b) When obtaining foams with complex and irregular shapes, foams that require dimensional accuracy, or composite foams with different compositions, the product shape, i.e. 2
It is difficult to design the cavity of the primary mold to give the secondary mold an appropriate shape and expansion ratio, and it will become increasingly difficult to develop foamed products that require high performance in the future. (c) In the primary crosslinking process, it is necessary to charge more than 100% of the foamed rubber compound into the cavity, so some protrusion occurs, material loss is unavoidable, and a finishing process is required to remove this protrusion. Become. Furthermore, the cell structure in this protruding portion is destroyed during finishing, reducing the quality of the closed cell foam.
This can cause negative effects such as a decline in product quality and variations. Purpose of the Invention The present invention was made in order to solve the drawbacks of the conventional cross-linking foaming process, which is a two-step high-pressure foaming method and uses two types of molds, in the production of rubber foam molded products as described above. It has physical properties equivalent to or better than closed cell foam obtained by the conventional high-pressure two-stage foaming method, and can produce high-quality foam molded products at low cost by reducing man-hours, mold costs, materials, etc. The object of the present invention is to provide a resource-saving and energy-saving manufacturing method that can be manufactured with high productivity. Structure of the Invention The present invention is a direct molding method using only a product mold, and consists of the following two inventions. First, the first aspect of the present invention is to fill a product mold with a foaming compound in an amount equal to or less than the cavity capacity in advance so as to obtain the necessary foaming ratio, and to fill the surplus space of the cavity with high pressure from the outside. By introducing and filling a gas such as air or nitrogen gas (approx. 10 kg/cm 2 ), keeping it airtight and maintaining a pressurized state, crosslinking can be achieved to some extent while suppressing excessive preliminary foaming of the foaming compound due to heating. This is a method in which foaming and crosslinking are completed by allowing the foam to proceed, then releasing the introduced high-pressure gas and continuing heating. In addition, a second invention according to the present invention basically utilizes the technical means of the first invention, but a foaming method is provided in which a small amount of foaming agent is blended into a part of the cavity of a product mold. The same method as in the first invention is carried out by charging two or more types of foaming compounds with different amounts of foaming agents, such as charging a foaming compound with a larger amount of foaming agent than the above compound into other parts of the cavity. By the method of
This is a method of integrally molding a low-density foamed portion and a firm, relatively high-density foamed portion at the same time. Functions, Effects, and Modes of the Invention The method of the present invention is similar in principle to the conventional high-pressure two-stage foaming method. That is, they are the same in that the crosslinking process is carried out in two stages: primary crosslinking and secondary crosslinking. However, the method is completely different from the conventional high-pressure two-stage foaming method. In other words, by omitting the use of a conventional primary mold, filling the product mold directly with the foaming compound, and introducing and filling the product mold with a high-pressure gas, we can suppress excessive preliminary foaming of the foaming compound due to heating. Crosslinking is allowed to proceed to a certain extent, then the gas is released, and heating is continued to complete foaming and crosslinking, and the two-step crosslinking is performed in a series of steps. Therefore, compared to the conventional high-pressure two-stage foaming method, the number of man-hours is reduced, and workability and productivity can be greatly improved. In addition, since a primary mold is not required, mold costs can be greatly reduced, and unlike conventional methods, protruding parts do not occur during the primary crosslinking process, and the finishing process of the primary crosslinked product is no longer necessary. It is also possible to prevent bubbles from breaking in the protruding portion. Furthermore, it is possible to easily produce closed-cell foams with complex irregular shapes, which have been difficult to obtain using conventional high-pressure two-stage foaming methods. In addition, in the method of the present invention, crosslinking is allowed to proceed to a certain extent while suppressing excessive preliminary foaming of the foaming compound due to heating (primary heating) under a pressurized state by a gas body, and then the gas pressure is released. Since foaming and crosslinking are completed by subsequent heating (secondary heating), it is preferable to set the temperature of the second heating higher than that of the first heating. In addition, the second invention according to the present invention is to foam and crosslink two or more foaming compounds containing different amounts of foaming agents by the above-mentioned method, and to form a low-foaming part and a high-foaming part, and thus to improve density and hardness. , parts with different physical properties such as heat resistance are integrally molded at the same time. Conventionally, floats for automobile carburetors, for example, often had complex irregular cross-sections due to the required performance. Moreover, it is required to have parts that require light weight and parts that require strength at the same time.
For this reason, some floats had movable metal arms firmly attached to the float body, others had magnets embedded in them. However, these metal parts have to be attached to the primary cross-linked structure, which poses a problem in that extra attachment work is required. On the other hand, it is conceivable that the above-mentioned parts requiring strength are made of a rubber foam with a low expansion ratio and high hardness, and are integrally molded with a lightweight part with a high expansion ratio. However, when this is carried out using the conventional high-pressure two-stage foaming method, each primary crosslinked product is molded separately.
After cooling and solidifying this and taking it out, it is necessary to perform secondary crosslinking in a product mold. Therefore, once cooled,
Even if the solidified primary crosslinked product is subjected to secondary crosslinking, the fusion and adhesion between the low expansion ratio part and the high expansion ratio part will not be sufficient, and the boundary will easily break, and two primary molds will be required, making it difficult to manufacture. There are also problems in terms of workability, productivity, and cost, as the number of steps increases and becomes complicated. However, in the second invention according to the present invention, it is sufficient to use only one product mold, and furthermore,
The primary crosslinked product that has been primary crosslinked by heating is cooled,
Since the secondary crosslinking treatment is performed as it is without being solidified, the effect of sufficiently high fusion and adhesion between the low expansion ratio portion and the high expansion ratio portion can be obtained. Furthermore, only one mold is needed for the product, and the two-step crosslinking is performed in a series of single steps.
It has excellent workability and productivity, and is also advantageous in terms of cost. It is most preferable from the viewpoint of fusion and adhesion that the foaming compounds of the low-foaming part and the high-foaming part are composed of the same composition except for changing the amount of the foaming agent, but this is not necessarily the case. They may be composed of different compositions as long as they differ widely in terms of physical properties, etc. Although the above explanation focuses on one product, it is also possible to provide a product mold with a plurality of cavities and simultaneously manufacture a plurality of products in one process. As raw rubber, all the rubber used for manufacturing rubber foam can be used, for example, in addition to natural rubber,
Synthetic rubbers such as chloroprene rubber, nitrile rubber, SBR, high styrene rubber, and butyl rubber can be used alone or in combination, and various raw material rubbers such as copolymers or blend polymers of rubber and synthetic resins can also be used. In addition, synthetic resins blended into raw rubber include phenol resin, PVC,
Various resins such as styrene are known. Further, as the blowing agent, conventionally well-known inorganic blowing agents and organic blowing agents can be used. EXAMPLES The present invention will be specifically explained with reference to Examples below. Note that the number of parts indicates parts by weight. Example 1 In this example, an example of a float for an automobile fuel gauge is shown. Composition of the foaming compound: NBR 80 parts PVC 20 parts phenolic resin 60 parts carbon black 30 parts ZnO 5 parts stearic acid 1 part vulcanization accelerator (DM 1.5 parts CZ 0.5 parts) 2 parts blowing agent (DPT) 6 parts urea Foaming aid: 2 parts Sulfur: 30 parts The above composition is kneaded, rolled or extruded to form a slab, cut into a desired shape and weight that is less than the cavity capacity of the product mold, weighed and molded. Prepare it. For example, as shown in Figure 1 (longitudinal sectional view) and Figure 2 (plan view of the parting surface), the flat type (cuboid cavity with length: 5 cm, width: 8 cm, and thickness: 1 cm) has a density of 0.25 g/ In order to obtain a float for a fuel gauge of cm 3 , 10 g of foaming compound 2 should be charged into a product mold cavity 1 of 40 cm 3 .
A packing groove 6 is provided on the parting surface around the capit 1 of the split mold 3 so that the airtightness of the capit y space is maintained, and a rubber packing 4 is fitted into the groove 6. While pressurizing high-pressure air (9 to 9.8 Kg/cm 3 ) from the introduction pipe 5, the mold is heated while being clamped with a pressure press. Heating was carried out for 18 minutes at approximately 130°C (vapor pressure 2Kg/cm 3 ), then the high pressure was released, and the temperature was lowered to approximately 165°C (vapor pressure) with the pressure press still clamped.
6.5Kg/cm 3 ) and heated for 30 minutes to complete foaming and crosslinking. Then, while keeping the mold clamped, the steam in the pressure press is switched to cooling water and cooled for 10 minutes to solidify the product, then the pressure press and mold are opened and the product is taken out. Example 2 In this example, an example of a float for an automobile carburetor is shown. The same foaming compound as in Example 1 was extruded using rod shapes 21a and 21b as shown in Fig. 3, cut to the required length and weight, and weighed. Flowate body portion 21a and arm portion 21b are charged into the mold shown in the plan view of the parting surface to a required cavity capacity or less. In the above product mold as well, similarly to the mold used in Example 1, a packing groove 61 is provided on the parting surface around the cap 11, and a rubber packing 41 is fitted into the groove 61. The mold was clamped with a pressure press, heated at approximately 130°C (vapor pressure 2Kg/cm 3 ) for 30 minutes while introducing N 2 gas (9.8Kg/cm 3 ) from the introduction pipe 51, and then the N 2 gas was released. Then, while keeping the mold clamped, the pressure press temperature was raised to about 170°C (vapor pressure 7Kg/cm 3 ), and heating was continued for 30 minutes to complete foaming and crosslinking. After that, switch the steam of the pressure press to cooling water,
Cool in water for 15 minutes to solidify the product, then release the pressure press, open the mold, and remove the product. We were able to simultaneously mold a product in which the arm part was firmly fused to the float body. Example 3 This example shows an example of a cover bottom having a complicated pattern on the bottom surface. Composition of the foaming compound: NR 100 parts * Nipol-2007 30 parts ZnO 5 parts Stearic acid 1 part Accelerator (DM) 0.6 parts Magnesium carbonate 50 parts Calcium carbonate 50 parts Process oil 15 parts Sulfur Yellow 3 parts Blowing agent (DPT) 5 Part Urea-based foaming aid 5 parts *) Styrene (85%)-butadiene (15%) copolymer, manufactured by Nippon Zeon Co., Ltd. The above composition was kneaded and rolled to form a slab 2.
2, as shown in FIG. 6 (longitudinal cross-sectional view) and FIG. 7 (plan view of the parting surface), the cavity is filled to less than the required cavity capacity, and the packing groove 62 provided on the parting surface around the cavity 12 is airtightly filled. Insert the rubber gasket 42, clamp the mold with a pressure press, and heat it at about 125°C (steam pressure 1.4Kg/cm 2 ) for 10 minutes while injecting N 2 gas (9.8Kg/cm 2 ) from the introduction pipe 52.
Heating for 1 minute, then releasing the N 2 gas, and heating at 150℃ (vapor pressure 4Kg/cm 2 ) for 10 minutes while keeping the mold clamped.
Heat for a minute to complete foaming and crosslinking, release the pressure press, open the mold and take out the product. The physical properties of the foams obtained in Examples 1 to 3 above are shown in Tables 1 and 2 below.

【表】【table】

【表】 前記実施例に示される如く、従来の高圧2段発
泡法に比較して、本発明の方法は特に発泡コンパ
ウンドの組成を変更する必要がなく、加圧ガスの
導入管のパルブ操作のみであり、また型入れ、型
出しが1回で済み、しかもはみ出しが発生せず、
1次架橋物の仕方工程も不要となり、はみ出し部
分の気泡破壊も防止でき、さらに従来の高圧2段
発泡法では得ることが難かしかつた複雑異形の独
立気泡の発泡体が容易に製造できた。 実施例 4 前記実施例1に示す組成と同一の発泡コンパウ
ンドにより、前記実施例2についての第3図に示
すようなロツド状21aに押出し、所要の長さ、
重量に裁断してフロート本体部とした。一方、発
泡剤の配合量を3部とする以外は前記実施例1に
示す組成と同一の発泡コンパウンドにより、第3
図の21bで示すようなロツド状に押出し、所要
の長さ、重量に裁断してアーム部とした。 上記フロート本体部21a及びアーム部21b
を第4図及び第5図に示す金型に仕込み、前記実
施例2と全く同様にして自動車キヤプレター用フ
ロートを同時成型した。高発泡のフロート本体
(密度0.29g/cm3)に堅固なアーム部(密度0.90
g/cm3)が強固に固着された製品が得られた。
[Table] As shown in the above examples, compared to the conventional high-pressure two-stage foaming method, the method of the present invention does not require any particular change in the composition of the foaming compound, and only requires pulving of the pressurized gas introduction pipe. In addition, only one mold insertion and mold removal is required, and no protrusion occurs.
It eliminates the need for a primary crosslinking process, prevents bubble collapse in protruding areas, and facilitates the production of complex, irregularly shaped, closed-cell foams that are difficult to obtain using conventional high-pressure two-stage foaming methods. Ta. Example 4 A foaming compound having the same composition as that shown in Example 1 was extruded into a rod shape 21a as shown in FIG.
It was cut into weight pieces to make the float body. On the other hand, a third foaming compound was prepared using the same foaming compound as shown in Example 1 except that the amount of foaming agent was changed to 3 parts.
It was extruded into a rod shape as shown by 21b in the figure, and cut to the required length and weight to form an arm portion. The float main body part 21a and the arm part 21b
was charged into the mold shown in FIGS. 4 and 5, and a float for an automobile capretor was simultaneously molded in exactly the same manner as in Example 2. Highly foamed float body (density 0.29g/cm 3 ) and solid arm part (density 0.90
A product was obtained in which the weight ratio (g/cm 3 ) was firmly fixed.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は実施例1で用いた金型の縦断面図、第
2図は第1図に示す金型のパーテイング面を示す
平面図、第3図は実施例2及び4で用いた発泡・
架橋前の発泡コンパウンド成型物の部分斜視図、
第4図は実施例2及び4で用いた金型の縦断面
図、第5図は第4図に示す金型のパーテイング面
を示す平面図、第6図は実施例3で用いた金型の
縦断面図、第7図は第6図に示す金型のパーテイ
ング面を示す平面図である。 1,11,12……金型キヤビテイ、2,21
a,21b,22……発泡コンパウンド、5,5
1,52……導入管。
FIG. 1 is a vertical cross-sectional view of the mold used in Example 1, FIG. 2 is a plan view showing the parting surface of the mold shown in FIG. 1, and FIG.
A partial perspective view of a foamed compound molded product before crosslinking,
Fig. 4 is a vertical cross-sectional view of the mold used in Examples 2 and 4, Fig. 5 is a plan view showing the parting surface of the mold shown in Fig. 4, and Fig. 6 is the mold used in Example 3. FIG. 7 is a plan view showing the parting surface of the mold shown in FIG. 6. 1, 11, 12... Mold cavity, 2, 21
a, 21b, 22... Foaming compound, 5, 5
1,52...Introduction pipe.

Claims (1)

【特許請求の範囲】 1 ゴム発泡成型品の製造において、製品成型用
金型キヤビテイに、予め必要な発泡倍率になるよ
うに金型キヤビテイ容量以下の量のゴムまたはゴ
ム及び合成樹脂の混合物に発泡剤を配合したゴム
系組成物を装入し、その際に生ずる金型キヤビテ
イの余剰の空間に外部から高圧のガス体を導入、
充満して加圧状態に保ちながら加熱し、ゴム系組
成物の発泡を抑制しながら架橋をある程度進行せ
しめ、その後高圧のガス体を解放し、さらに加熱
を続けて発泡、架橋を完結させることを特徴とす
るゴム発泡成型品の製造方法。 2 ゴム発泡成型品の製造において、製品成型用
金型キヤビテイに、ゴムまたはゴム及び合成樹脂
の混合物に異なつた量の発泡剤を配合した2種以
上のゴム系組成物をそれぞれ予め必要な発泡倍率
になるように金型キヤビテイの容量以下の量で装
入し、その際に生ずる金型キヤビテイの余剰の空
間に外部から高圧のガス体を導入、充満して加圧
状態に保ちながら加熱し、前記ゴム系組成物の発
泡を抑制しながら架橋をある程度進行せしめ、そ
の後高圧のガス体を解放し、さらに加熱を続けて
発泡、架橋を完結させ、低密度発泡部分と堅固な
比較的高密度の発泡部分とを同時に一体成型する
ことを特徴とするゴム発泡成型品の製造方法。
[Scope of Claims] 1. In the production of rubber foam molded products, rubber or a mixture of rubber and synthetic resin is foamed in an amount less than the capacity of the mold cavity in advance to obtain the required foaming ratio in the mold cavity for molding the product. The rubber composition containing the agent is charged, and a high-pressure gas is introduced from the outside into the excess space of the mold cavity that is created at that time.
Fill the rubber composition and heat it while keeping it in a pressurized state to allow crosslinking to proceed to some extent while suppressing foaming of the rubber composition, then release the high pressure gas and continue heating to complete foaming and crosslinking. A manufacturing method for characteristic rubber foam molded products. 2. In the production of rubber foam molded products, two or more rubber compositions containing different amounts of blowing agents in rubber or a mixture of rubber and synthetic resin are added to the mold cavity for molding the product at the required expansion ratio. A high-pressure gas is introduced from the outside into the excess space of the mold cavity that is created at this time, filling it and heating it while maintaining the pressurized state. Crosslinking is allowed to proceed to some extent while suppressing foaming of the rubber composition, and then a high-pressure gas is released, and heating is continued to complete foaming and crosslinking, forming a low-density foamed portion and a firm relatively high-density foamed portion. A method for manufacturing a rubber foam molded product, characterized by integrally molding a foamed part and a foamed part at the same time.
JP58140497A 1983-08-02 1983-08-02 Manufacture of rubber foamed and molded item Granted JPS6032613A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58140497A JPS6032613A (en) 1983-08-02 1983-08-02 Manufacture of rubber foamed and molded item

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58140497A JPS6032613A (en) 1983-08-02 1983-08-02 Manufacture of rubber foamed and molded item

Publications (2)

Publication Number Publication Date
JPS6032613A JPS6032613A (en) 1985-02-19
JPH0510208B2 true JPH0510208B2 (en) 1993-02-09

Family

ID=15270000

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58140497A Granted JPS6032613A (en) 1983-08-02 1983-08-02 Manufacture of rubber foamed and molded item

Country Status (1)

Country Link
JP (1) JPS6032613A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11780621B2 (en) 2008-05-19 2023-10-10 Max Co., Ltd. Brake system of wire reel in reinforcing bar binding machine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11780621B2 (en) 2008-05-19 2023-10-10 Max Co., Ltd. Brake system of wire reel in reinforcing bar binding machine

Also Published As

Publication number Publication date
JPS6032613A (en) 1985-02-19

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