JPS61135714A - Molding of copolymer of tetrafluoroethylene and molding mold therefor - Google Patents

Molding of copolymer of tetrafluoroethylene and molding mold therefor

Info

Publication number
JPS61135714A
JPS61135714A JP25732784A JP25732784A JPS61135714A JP S61135714 A JPS61135714 A JP S61135714A JP 25732784 A JP25732784 A JP 25732784A JP 25732784 A JP25732784 A JP 25732784A JP S61135714 A JPS61135714 A JP S61135714A
Authority
JP
Japan
Prior art keywords
molding
copolymer
mold
coated
tetrafluoroethylene
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP25732784A
Other languages
Japanese (ja)
Other versions
JPH0224648B2 (en
Inventor
Yoshitaka Yoshida
由孝 吉田
Kasuke Ishii
石井 嘉右
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.)
YOSHIDA S K T GOUSHI
Chemours Mitsui Fluoroproducts Co Ltd
Original Assignee
YOSHIDA S K T GOUSHI
Du Pont Mitsui Fluorochemicals Co Ltd
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 YOSHIDA S K T GOUSHI, Du Pont Mitsui Fluorochemicals Co Ltd filed Critical YOSHIDA S K T GOUSHI
Priority to JP25732784A priority Critical patent/JPS61135714A/en
Publication of JPS61135714A publication Critical patent/JPS61135714A/en
Publication of JPH0224648B2 publication Critical patent/JPH0224648B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To prevent the adhesion of copolymer of tetrafluoroethylene to the mold as well as the foaming of molded product by a method wherein the copolymer of tetrafluoroethylene and one or two kinds of comonomer, shown by the formula I, is heated to melt it, thereafter, the copolymer is cooled and solidified in the metallic mold, coated by polyallylenesulfide (PAS). CONSTITUTION:The dispersion coating medium or powder coating medium of PAS is coated on the metallic mold by the conventional technique such as spraying, dipping, brushing, roller coating, fludization dip coating or the like and, subsequently, is baked at the temperature of 300-450 deg.C. Heating and melting are effected outside of the metallic mold or in a barrel in case of injection molding while they are effected in a pot in case of transfer molding. Successively, the molten copolymer is poured into the metallic mold coated by PAS. On the other hand, the copolymer is heated and molten in the metallic mold, coated by PAS, in case of compression molding, rotary molding or the like and, successively, is cooled and solidified in the metallic mold.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、成形品の剥離性が良好で、且つ成形品に気
泡の発生のないテトラフルオロエチレン共重合体の成形
法とこの成形に使用する金型に関する。
Detailed Description of the Invention (Field of Industrial Application) This invention provides a method for molding a tetrafluoroethylene copolymer that has good peelability in molded products and does not generate bubbles in molded products, and a method for molding tetrafluoroethylene copolymers that can be used in this molding. Regarding molds.

(従来技術) テトラブルオロエチレン共重合体樹脂は優れた耐熱、耐
薬品、電気的特性、更には非粘着、低摩擦性などフッ素
樹脂特有の性質を有するとともに、高温で溶融して可塑
性を帯びるため、射出、トランスファー、圧縮、回転及
びキャスティングなどの成形法を用いて成形品を製造で
きる樹脂として知られている。
(Prior art) Tetrofluoroethylene copolymer resin has excellent heat resistance, chemical resistance, electrical properties, non-stick properties, low friction properties, and other properties unique to fluororesins, and it melts at high temperatures and becomes plastic. Therefore, it is known as a resin that can be used to produce molded products using molding methods such as injection, transfer, compression, rotation, and casting.

(発明が解決しようとする問題点) 斯かるテトラフルオロエチレン共重合体の成形における
第1の問題とし、て金型への樹脂の固着がある。
(Problems to be Solved by the Invention) The first problem in molding such a tetrafluoroethylene copolymer is that the resin sticks to the mold.

先に述べた通シテトラブルオロエチレン共重合体は非粘
着性のポリマーで、非溶融状態(固体状態)では流体及
び接着剤のような粘稠な物質によっても殆んど濡れるこ
とがない。しかしながらテトラフルオロエチレン共重合
体樹脂が溶融して液体状態になった場合、表面張力が低
下して多くの固体物質を濡らすことが可能となシ、この
樹脂が固化する際に接触する固体物質の表面へ固着する
。そのため、金型への固着現象が生ずる。
The above-mentioned polyolefin ethylene copolymer is a non-adhesive polymer, and in its non-molten state (solid state), it is hardly wetted by fluids and viscous substances such as adhesives. However, when the tetrafluoroethylene copolymer resin melts into a liquid state, the surface tension decreases and it becomes possible to wet many solid materials. Sticks to surfaces. Therefore, a phenomenon of sticking to the mold occurs.

第2の問題は成形品の発泡の問題である。The second problem is foaming of the molded product.

テトラフルオロエチレン共重合体を射出成形又は押出成
形のような高い圧力で成形する場合には溶融状態の樹脂
中に樹脂の分解ガス及び空気などの気体物質が含まれて
いても、ガス抜きを比較的容易に行なうことができるた
め問題とはならないが、回転成形のように無加圧状態で
、且つ金型の温度が高い場合には多量の分解ガスが発生
し、しかもガスの除去が困難であるため、成形品中に気
泡が発生する。
When molding tetrafluoroethylene copolymer under high pressure such as injection molding or extrusion molding, even if the molten resin contains gaseous substances such as resin decomposition gas and air, degassing is compared. This is not a problem because it is easy to carry out, but when there is no pressure and the temperature of the mold is high, as in rotational molding, a large amount of decomposed gas is generated, and it is difficult to remove the gas. This causes bubbles to form in the molded product.

第1の問題点即ち成形品の金型からの離型については金
型表面の研磨或いは金型表面へシリコン系離型剤などの
離型剤を塗布することによって成形品の金型への固着問
題を解決して来たが、表面研磨は研磨に多くの手間が掛
シ、且つ寿命が短かく、離形性も十分でない。また離形
剤の使用する方法は、シリコン系離形剤でもフッ素樹脂
の成形温度に耐えられず、更に離形剤が成形品の表面に
付着することによ構成形品の表面状態を悪化”すること
がらシ、またその離形効果のある時間も短かいという欠
点がある。
The first problem, that is, the release of the molded product from the mold, can be fixed by polishing the mold surface or applying a mold release agent such as a silicone mold release agent to the mold surface. Although the problem has been solved, surface polishing requires a lot of time and effort, has a short service life, and does not have sufficient mold releasability. In addition, the method of using a mold release agent is such that even silicone mold release agents cannot withstand the molding temperature of fluororesin, and furthermore, the mold release agent adheres to the surface of the molded product, worsening the surface condition of the molded product. However, there are disadvantages in that the mold release effect is short-lived.

また第2の問題点即ち成形品中に気泡が発生する問題の
解決については樹脂中に亜鉛、錫などの安定剤を加える
方法が提案されているが、これ等金属の添加は耐酸、耐
アルカリ性の低下、電気絶縁性の低下及び不純物が含ま
れていないというフッ素樹脂の特性を損逢うものであり
、好ましくない。
In addition, to solve the second problem, that is, the problem of air bubbles occurring in molded products, it has been proposed to add stabilizers such as zinc and tin to the resin, but the addition of these metals has a high acid and alkali resistance. This is undesirable because it impairs the properties of fluororesin, such as a decrease in electrical insulation, a decrease in electrical insulation, and the absence of impurities.

(問題点を解決するための手段) 以上の問題点を解決するため、本願第1発明は、テトラ
フルオロエチレンと、下記式(式中R7tはH又は炭素
数1〜5のフルオロアルキル基、R/、は炭素数1〜5
のフルオロアルキル基、Xl、 X、及びX、はF又は
H)のコモノマーの1種又は2種以上との共重合体を加
熱、溶融し、ポリアリレンスルフィド(以下、PASと
記す)で被覆した金型中で冷却、固化して成形するテト
ラブルオロエチレン共重合体の成形法な提案するもので
ある。
(Means for Solving the Problems) In order to solve the above problems, the first invention of the present application provides tetrafluoroethylene and the following formula (where R7t is H or a fluoroalkyl group having 1 to 5 carbon atoms, R /, is carbon number 1-5
A copolymer of one or more comonomers of fluoroalkyl group, Xl, X, and This paper proposes a method for molding a tetrafluoroethylene copolymer by cooling and solidifying it in a mold.

本願第2発明は、PASで被覆したテトラフルオロエチ
レン共重合体成形用金型を提案するものである。
The second invention of the present application proposes a mold for molding a tetrafluoroethylene copolymer coated with PAS.

この発明で使用するPASとしては、ポリフェニレンス
ルフィド(以下、PPSと記す)等を例示することがで
きる。
Examples of the PAS used in this invention include polyphenylene sulfide (hereinafter referred to as PPS).

なおPARは成可く純度の高いものが好ましく、例えば
醸化チタンなどの顔料や充填剤の過度の添加、例えばこ
れ等の充填剤を50−以上を含むPARは屡々離形性を
低下させることがある。
It should be noted that PAR is preferably one that is as pure as possible and has high purity; for example, excessive addition of pigments and fillers such as fermented titanium, for example, PAR containing 50 or more of these fillers, often reduces mold releasability. There is.

またPARの被覆表面は成可く平滑なことが好ましく、
塗膜の表面状態が悪いと離形性が不充分な場合がある。
It is also preferable that the PAR coating surface be smooth and smooth.
If the surface condition of the coating film is poor, the mold releasability may be insufficient.

なお塗膜の表面状態が悪く、離型性が不充分な場合には
その表面を研磨し、再焼付けを行なうことにより離形性
を向上させることができる。
In addition, if the surface condition of the coating film is poor and the mold releasability is insufficient, the mold releasability can be improved by polishing the surface and performing re-baking.

金型へのPARの被覆は常法にしたがって行なわれる。The mold is coated with PAR according to a conventional method.

例えばPP8の分散液塗料又は粉体塗料などを、吹き付
け、浸漬、刷毛塗シ、ローラー掛け、流動浸漬その他の
慣用の手法により金型に塗布し、次いで500〜450
℃の温度で焼付けを行う。
For example, a dispersion paint or powder paint of PP8 is applied to the mold by spraying, dipping, brushing, rolling, fluid dipping, or other conventional methods, and then
Baking is carried out at a temperature of °C.

一方この発明の成形法に好適なテトラフルオ(登碌商標
) ロエチレン共重合体としては例えばテフロンPF^、テ
フロンFEP 、テフロンEPE [三Jlデ(登碌商
標) エポン70ロケミカル(株)製品〕及びテクゼルETE
E (デュポン製品)などの商品名で知られている熱流
動性フッ素樹脂を挙げることができる。
On the other hand, examples of the tetrafluoroethylene copolymer suitable for the molding method of the present invention include Teflon PF^, Teflon FEP, Teflon EPE [San Jl De (registered trademark) Epon 70 Rochemical Co., Ltd. product], and Tekzel. ETE
Examples include thermofluid fluororesins known under trade names such as E (DuPont product).

テクゼクETFEを使用する場合凡そ300〜400℃
の温度で、テフロンPFA 、テフロンFEP、f”フ
ロンEPEの場合には330〜450℃の温度で加熱溶
融する。
When using Tekzeku ETFE, the temperature is approximately 300-400℃
In the case of Teflon PFA, Teflon FEP, and f'' flon EPE, it is heated and melted at a temperature of 330 to 450°C.

この加熱、溶融拡射出成形、トランスファ成形等の場合
は金型外で行う。即ち、射出成形の場合にはバレル内で
、またトランスファ成形の場合にはポット内で行なわれ
、次いでPASで被覆した金型内に注入する方法が採ら
れる。
This heating, melt expansion injection molding, transfer molding, etc. are performed outside the mold. That is, in the case of injection molding, it is carried out in a barrel, and in the case of transfer molding, it is carried out in a pot, and then it is injected into a mold coated with PAS.

一方圧縮成形、回転成形等の場合にはPASで被覆した
金型内で加熱溶融し、次いで金型内で冷却、固化する方
法が採られる。
On the other hand, in the case of compression molding, rotational molding, etc., a method is adopted in which the material is heated and melted in a mold coated with PAS, and then cooled and solidified in the mold.

(発明の効果) か\る成形法、即ち本願第1発明の成形法はテトラフロ
ルオロエトレン共重合体の金型への固着と成形品の発泡
という、その発生原因を異にする現象を一挙に解決する
ものである。
(Effects of the Invention) The above molding method, that is, the molding method of the first invention of the present application, simultaneously solves the problems of sticking of the tetrafluoroethrene copolymer to the mold and foaming of the molded product, which have different causes. This will solve the problem.

一方本願第2発明において金製はPASの被覆によシテ
トラブルオロエチレン共重合体の熱分解そのものを低減
できるだけで表<、腐食性の熱分解ガスが直接金属性の
金型面との接触を避けることができるため、テトラフル
オロエチレン共重合体成形用金型の材質として従来のよ
うにハステロイやステンレスのような耐食性合金を使用
することなく、安価なカーボンスチールで金型を製作す
ることができる。
On the other hand, in the second invention of the present application, the PAS coating can only reduce the thermal decomposition of the tetrafluoroethylene copolymer and prevent the corrosive pyrolysis gas from coming into direct contact with the metal mold surface. Therefore, it is possible to manufacture molds using inexpensive carbon steel instead of using conventional corrosion-resistant alloys such as Hastelloy and stainless steel as materials for molds for molding tetrafluoroethylene copolymer. .

更にPA8は金製に焼付けられているため、通常の離形
剤のように消耗することがなく、その表面硬度も高いた
め、離形効果を長く保つことができる。
Furthermore, since PA8 is baked into gold, it does not wear out like normal mold release agents, and its surface hardness is high, so it can maintain its mold release effect for a long time.

(実施例) 以下1、この発明の実施例を示す。(Example) Embodiment 1 of the present invention will be described below.

実施例1 5QXIQQ X 2.5mの鉄板(材質8841)を
溶剤脱脂、空焼きを行ない、その表面の半分にpps(
登碌商標) 水性分散塗料(サスティールC−400:保土ケ谷化学
工業製品)を約20pmlk布し乾燥した後、590℃
で50分間焼付けを行なった。
Example 1 A 5QXIQQ x 2.5m iron plate (material 8841) was degreased with solvent and air-baked, and half of its surface was coated with pps (
Approximately 20 pmlk of water-based dispersion paint (Sasteel C-400: Hodogaya Chemical Industry Product) was applied on a cloth and dried at 590°C.
Baking was performed for 50 minutes.

この鉄板を加熱圧縮成形用金型の底型とし、その上に厚
さ1gmのテフロンPFAシート〔三井・デュポンケミ
カル(株)製品〕を載せ、340〜350℃の炉中で加
熱し、PFAシートを溶融した。
This iron plate was used as the bottom mold of a mold for hot compression molding, and a 1 gm thick Teflon PFA sheet (manufactured by Mitsui DuPont Chemical Co., Ltd.) was placed on top of it, heated in a furnace at 340 to 350°C, and the PFA sheet was melted.

次いでこれを炉よシ取り出し、成形圧50隔−で圧縮、
冷却を行なった。
Next, this was taken out of the furnace and compressed at a molding pressure of 50 degrees.
Cooling was performed.

冷却後、上記鉄板(底型)を金型の外筒より取り出した
ところPPSを被覆した部分にはPFAが固着していな
かった(剥離強度0(j)。
After cooling, the iron plate (bottom mold) was taken out from the outer cylinder of the mold, and PFA was not adhered to the PPS-covered part (peel strength 0(j)).

一方PPSを被覆しなかった部分にはPFAが強く固着
しており、その剥離強度は5.9q/csであった。
On the other hand, PFA was strongly adhered to the part not coated with PPS, and its peel strength was 5.9 q/cs.

実施例2 直径200mの半球状の基金型にpps水性分散V−1
採土ケ谷化学工業製品)を塗布し、330℃で50分焼
付けを行なった。次いでこのPPS被覆表面を耐水研磨
紙(CC−600)で研磨し、560℃で60分間再焼
付を行なった。
Example 2 PPS aqueous dispersion V-1 in a hemispherical fund shape with a diameter of 200 m
(Odugaya Chemical Industry product) was applied and baked at 330°C for 50 minutes. The PPS coated surface was then polished with waterproof abrasive paper (CC-600) and rebaked at 560°C for 60 minutes.

この金型に粒径200μのテフロンPFA粉末(三井・
デュポンフロロケミカル製品)270fを入れ、温度5
70℃の炉中で2時間二輪回転法によυ直径200■、
肉厚的2−の中空球を成形した。
In this mold, Teflon PFA powder with a particle size of 200μ (Mitsui)
DuPont fluorochemical product) 270f was added, and the temperature was 5.
υ diameter 200■ by two-wheel rotation method in a 70℃ oven for 2 hours,
A 2-thick hollow sphere was molded.

成形品には発泡はみられず、また成形品が金型に固着す
ることもなかった。
No foaming was observed in the molded product, and the molded product did not adhere to the mold.

特許出願人 合資会社 吉日ニス・ケイ・テイ手続補正
書(6引 昭和60年1 月17日
Patent Applicant: Limited Partnership Company Kichihi Nis.K.T. Procedural Amendment (Reference 6, January 17, 1985)

Claims (2)

【特許請求の範囲】[Claims] (1)テトラフルオロエチレンと、 下記式 ▲数式、化学式、表等があります▼及び▲数式、化学式
、表等があります▼ (式中Rf_1はH又は炭素数1〜5のフルオロアルキ
ル基、 Rf_2は炭素数1〜5のフルオロアル キル基、 X_1、X_2及びX_3はF又はH) のコモノマーの1種又は2種以上との共重合体を加熱、
溶融し、ポリアリレンスルフィドで被覆した金型中で冷
却、固化して成形することを特徴とするテトラフルオロ
エチレン共重合体の成形法。
(1) Tetrafluoroethylene and the following formulas ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ and ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ (In the formula, Rf_1 is H or a fluoroalkyl group with 1 to 5 carbon atoms, Rf_2 is Heating a copolymer with one or more comonomers of a fluoroalkyl group having 1 to 5 carbon atoms,
A method for molding a tetrafluoroethylene copolymer, which is characterized by melting, cooling and solidifying in a mold coated with polyarylene sulfide, and molding.
(2)ポリアリレンスルフィドで被覆したことを特徴と
するテトラフルオロエチレン共重合体成形用金型。
(2) A mold for molding a tetrafluoroethylene copolymer, characterized in that it is coated with polyarylene sulfide.
JP25732784A 1984-12-07 1984-12-07 Molding of copolymer of tetrafluoroethylene and molding mold therefor Granted JPS61135714A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25732784A JPS61135714A (en) 1984-12-07 1984-12-07 Molding of copolymer of tetrafluoroethylene and molding mold therefor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25732784A JPS61135714A (en) 1984-12-07 1984-12-07 Molding of copolymer of tetrafluoroethylene and molding mold therefor

Publications (2)

Publication Number Publication Date
JPS61135714A true JPS61135714A (en) 1986-06-23
JPH0224648B2 JPH0224648B2 (en) 1990-05-30

Family

ID=17304819

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25732784A Granted JPS61135714A (en) 1984-12-07 1984-12-07 Molding of copolymer of tetrafluoroethylene and molding mold therefor

Country Status (1)

Country Link
JP (1) JPS61135714A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0473678U (en) * 1990-11-06 1992-06-29
JPH08145240A (en) * 1994-11-16 1996-06-07 Nichiei Intec Kk Piping support fitment for fixing base plate alone
EP0773093A1 (en) * 1995-11-08 1997-05-14 Hüls Aktiengesellschaft Coated mould for molding latex foamed articles

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0473678U (en) * 1990-11-06 1992-06-29
JPH08145240A (en) * 1994-11-16 1996-06-07 Nichiei Intec Kk Piping support fitment for fixing base plate alone
EP0773093A1 (en) * 1995-11-08 1997-05-14 Hüls Aktiengesellschaft Coated mould for molding latex foamed articles

Also Published As

Publication number Publication date
JPH0224648B2 (en) 1990-05-30

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