JPH02295710A - Reaction injection molding method - Google Patents

Reaction injection molding method

Info

Publication number
JPH02295710A
JPH02295710A JP11814989A JP11814989A JPH02295710A JP H02295710 A JPH02295710 A JP H02295710A JP 11814989 A JP11814989 A JP 11814989A JP 11814989 A JP11814989 A JP 11814989A JP H02295710 A JPH02295710 A JP H02295710A
Authority
JP
Japan
Prior art keywords
molding material
resin molding
foaming
resin
mold
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
Application number
JP11814989A
Other languages
Japanese (ja)
Inventor
Toshitaka Takahashi
敏貴 高橋
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.)
Mazda Motor Corp
Original Assignee
Mazda Motor Corp
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 Mazda Motor Corp filed Critical Mazda Motor Corp
Priority to JP11814989A priority Critical patent/JPH02295710A/en
Publication of JPH02295710A publication Critical patent/JPH02295710A/en
Pending legal-status Critical Current

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  • Injection Moulding Of Plastics Or The Like (AREA)

Abstract

PURPOSE:To enhance the foaming rate of the thick wall part of a resin molded product and to prevent a sink mark by mixing a high b.p. foaming agent with a resin molding material and coating the thick wall part molding part of a mold with an amine type foaming accelerator. CONSTITUTION:A high b.p. foaming agent having a b.p. higher than the reaction molding temp. of a resin molding material is preliminarily mixed with the resin molding material while the thick wall part molding part 6 of a mold 5 is coated with an amine type foaming accelerator 7 reacted with the isocyanate component in the above mentioned resin molding material and generating temp. due to the reaction higher than the b.p. of the above mentioned high b.p. foaming agent by spraying after the coating with a release agent. Then, the resin molding material is injected in the mold 5. By this method, in the thick wall part molding part of the mold 5, the temp. of the resin molding material becomes higher than the b.p. of the high b.p. foaming agent by the reaction of the foaming accelerator 7 applied to said part 6 and the isocyanate component in the resin molding material. Therefore, the foaming rate at the thick wall part molding part 6 becomes higher than that at a thin wall part molding part 8 by the contribution of the high b.p. foaming agent to the foaming of the resin molding material.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は反応射出成形方法に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to a reaction injection molding method.

(従来の技術) リブ等の厚肉部がある樹脂成形品を反応射出成形によっ
て得る場合、樹脂成形品には上記厚肉部が突出している
反対側の面、つまり裏面にヒヶと呼ばれる表面欠陥を生
じやすいことは一般に知られている。すなわち、このヒ
ケは樹詣の硬化収縮量が厚肉部とその周辺の薄肉部とで
相違するために生じるものである。
(Prior art) When a resin molded product with thick parts such as ribs is obtained by reaction injection molding, the resin molded product has a surface called a gap on the opposite side from which the thick part protrudes, that is, the back side. It is generally known that defects are likely to occur. In other words, this sink mark occurs because the amount of hardening and shrinkage of the tree is different between the thick part and the surrounding thin part.

上記ヒケの対策としては、 ■ 厚内部の片側にその反対側よりも肉厚が小さい薄肉
部を形成することにより、成形型における厚肉部成形部
の樹脂成形材料の流速がその周辺部と略同じになるよう
にする方法(特開昭62−111711号公報参照)、 ■ 厚肉部周辺の肉厚の変化を小さくする方法、■ 樹
脂成形材料を射出後に加圧する方法、■ 低収縮マイク
ロカプセルを樹脂成形材料中に混入する方法 等が知られている。
As a countermeasure for the sink marks mentioned above, ■ By forming a thin wall part on one side of the thick interior where the wall thickness is smaller than that on the other side, the flow velocity of the resin molding material in the thick part molded part of the mold is approximately equal to that in the surrounding area. (Refer to Japanese Unexamined Patent Publication No. 62-111711), ■ A method to reduce the change in wall thickness around the thick part, ■ A method to pressurize the resin molding material after injection, ■ Low-shrinkage microcapsules A method is known in which the compound is mixed into a resin molding material.

(発明が解決しようとする課題) しかし、上記■,■の方法では、樹脂成形品の形状に制
約を生ずるとともに、成形型の形状の変更を要求され、
上記■では加圧装置が別途必要になり、上記■では厚肉
部と薄肉部との収縮量の差という根本原因についての解
決を図るものでないため、大きな効果は期待できない。
(Problems to be Solved by the Invention) However, the methods ① and ② above impose restrictions on the shape of the resin molded product and require changes in the shape of the mold.
The above method (2) requires a separate pressurizing device, and the above method (2) does not attempt to solve the root cause of the difference in the amount of shrinkage between the thick portion and the thin portion, so no great effect can be expected.

すなわち、本発明の課題は、成形型の形状変更や特別な
装置の付加を行なうことなく、上記ヒケを効率良く解消
できるようにすることにある。
That is, an object of the present invention is to make it possible to efficiently eliminate the sink mark without changing the shape of the mold or adding any special equipment.

(課題を解決するための手段) 本発明は、このような課題に対して、反応射出成形にお
ける反応系を制御して厚肉部における樹脂成形材料の発
泡率を高め、上記ヒヶを防止するものである。
(Means for Solving the Problems) In order to solve these problems, the present invention controls the reaction system in reaction injection molding to increase the foaming rate of the resin molding material in the thick-walled parts, thereby preventing the above-mentioned cracks. It is something.

すなわち、そのための手段は、 ウレタン・ウレア系樹脂成形材料により厚肉部を有する
樹脂成形品を得る反応射出成形方法であって、 上記樹脂成形材料中にその反応成形温度よりも沸点が高
い高沸点発泡剤を混入しておく一方、成形型における上
記厚内部を成形する部分に、上記樹脂成形材料中のイソ
シアネート成分と反応し且つその反応による発熱温度が
上記高沸点発泡剤の沸点よりも高いアミン系発泡促進剤
を塗布しておいて、 上記樹脂成形材料を成形型に射出する、ことを特徴とす
るものである。
That is, the means for this purpose is a reaction injection molding method for obtaining a resin molded product having a thick wall part using a urethane/urea resin molding material, and the resin molding material contains a high boiling point that is higher than the reaction molding temperature of the resin molding material. While a blowing agent is mixed in, an amine that reacts with the isocyanate component in the resin molding material and whose exothermic temperature due to the reaction is higher than the boiling point of the high boiling point blowing agent is added to the part of the mold that molds the thick interior. The method is characterized in that the resin molding material is injected into a mold after applying a foaming accelerator.

(作用) 上記成形方法においては、成形型の厚肉部成形部では、
そこに塗布されたアミン系発泡促進剤と樹脂成形材料中
のイソシアネート成分との反応により、樹脂成形材料の
温度が高沸点発泡剤の沸点よりも高くなる。よって、こ
の厚肉部成形部では高沸点発泡剤が樹脂成形材料の発泡
に寄与することにより、その周辺部よりも樹脂成形材料
の発泡率が高くなり、ヒケの発生が防止される。つまり
、発泡率が高いということは、樹脂成形品はこの厚肉部
においては気孔部が多く、樹脂部が少ないということで
あり、この樹脂部が少なくなる分、収縮率が低くなり、
ヒケの原因である厚肉部と薄肉部との収縮量の差が小さ
くなるものである。
(Function) In the above molding method, in the thick-walled molding part of the mold,
Due to the reaction between the amine foaming accelerator applied thereto and the isocyanate component in the resin molding material, the temperature of the resin molding material becomes higher than the boiling point of the high boiling point foaming agent. Therefore, the high boiling point foaming agent contributes to the foaming of the resin molding material in this thick-walled molded part, so that the foaming rate of the resin molding material becomes higher than that in the surrounding area, and the occurrence of sink marks is prevented. In other words, a high foaming rate means that a resin molded product has many pores and a small amount of resin in the thick part, and the smaller the resin, the lower the shrinkage rate.
This reduces the difference in the amount of shrinkage between the thick portion and the thin portion, which is the cause of sink marks.

(発明の効果) 従って、本発明によれば、樹脂成形材料に高沸点発泡剤
を混入し、成形型の厚肉部成形部にアミン系発泡促進剤
を塗布するという簡単な手段により、樹脂成形品の厚内
部の発泡率を高め、成形型の形状変更や特別な装置の付
加を行なうことなく、ヒケを防止することができる。
(Effects of the Invention) Therefore, according to the present invention, resin molding can be carried out by a simple means of mixing a high boiling point foaming agent into a resin molding material and applying an amine foaming accelerator to the thick-walled molding part of the mold. By increasing the foaming rate in the thick interior of the product, it is possible to prevent sink marks without changing the shape of the mold or adding special equipment.

(実施例) 以下、本発明の実施例を図面に基づいて説明する。(Example) Embodiments of the present invention will be described below based on the drawings.

第1図には反応射出成形によって得る樹脂成形品1の一
部が示されている。この樹脂成形品1の厚肉部2は、樹
脂成形品1の片面にリブが設けられた部分であり、厚肉
部2の両側が薄肉部3ということになる。
FIG. 1 shows a part of a resin molded product 1 obtained by reaction injection molding. The thick portion 2 of the resin molded product 1 is a portion where a rib is provided on one side of the resin molded product 1, and both sides of the thick portion 2 are called thin portions 3.

上記反応射出成形に供する樹脂成形材料の配合は次の通
りである。
The formulation of the resin molding material used in the reaction injection molding is as follows.

A.ボリオールサイド ボリブロピレングリコール 平均分子量4000     84. 8重量部DET
DA (ジエチル トルエンジアミン>    15.0重量部錫触媒(ジ
オクチルチン ジラウレート)0.12重量部 アミン触媒(トリエチル ジアミン).  0.12重量部 カットガラスファイバー (径lOμ,繊維長100μ)24.4重量部B.イソ
シアネートサイド 変性MDI(ジフェニル メタンジイソシアネート)   120重量部高沸点発
泡剤(テトラ クロロエタン)   5重量部 上記高沸点発泡剤の沸点は146.2℃である。
A. Polyol side polypropylene glycol average molecular weight 4000 84. 8 parts by weight DET
DA (diethyltoluenediamine> 15.0 parts by weight Tin catalyst (dioctyltin dilaurate) 0.12 parts by weight Amine catalyst (triethyldiamine). 0.12 parts by weight Cut glass fiber (diameter lOμ, fiber length 100μ) 24.4 parts by weight Part B. Isocyanate side modified MDI (diphenylmethane diisocyanate) 120 parts by weight High boiling point blowing agent (tetrachloroethane) 5 parts by weight The boiling point of the above high boiling point blowing agent is 146.2°C.

第2図には上記樹脂成形品1を得るための成形型(金型
)5の一部が示されている。
FIG. 2 shows a part of a mold (mold) 5 for obtaining the resin molded product 1. As shown in FIG.

しかして、射出成形にあたっては、この成形型5におけ
る上記厚肉部2を成形する厚肉部成形部6に発泡促進剤
7を塗布するものであり、この発泡促進剤7の配合は次
の通りである。
Therefore, in injection molding, a foaming accelerator 7 is applied to the thick-walled part molding part 6 of the mold 5 where the thick-walled part 2 is formed, and the formulation of the foaming accelerator 7 is as follows. It is.

C.発泡促進剤 アミン1 ;TDA (}ルエン ジアミン)  0.5重量部 アミン2 ,TEDA (}リ エチレンジアミン) 0.5重量部 そして、上記発泡促進剤7は、上記成形型5の厚肉部成
形部6に対して、離型剤を塗布した後、スプレーにより
塗布するものである。
C. Foaming accelerator amine 1; TDA (}luenediamine) 0.5 parts by weight Amine 2, TEDA (}lyethylenediamine) 0.5 parts by weight. On the other hand, after applying a mold release agent, it is applied by spraying.

そうして、上記発泡促進剤7の塗布後、上述の樹脂成形
材料を成形型5に射出する。これにより、成形型5の厚
肉部成形部6では、そこに塗布された発泡促進剤7と樹
脂成形材料中のイソシアネート成分との反応により、樹
脂成形材料の温度が高沸点発泡剤の沸点よりも高くなる
After applying the foaming accelerator 7, the resin molding material described above is injected into the mold 5. As a result, in the thick-walled molding part 6 of the mold 5, the temperature of the resin molding material rises above the boiling point of the high-boiling point blowing agent due to the reaction between the foaming accelerator 7 applied thereto and the isocyanate component in the resin molding material. It also becomes more expensive.

すなわち、本例の場合、発泡促進剤7は、アミン1のT
DAが樹脂成形材料のインシアネート成分である変性M
DIと反応し、ウレア結合を有する高分子化合物を生成
し、アミン2のTEDAはこの反応の触媒的作用を呈す
る。そして、この反応はその速度が速く発熱量が大であ
って、当該厚内部成形部6においては、樹脂成形材料の
温度を高沸点発泡剤の沸点よりも高くするものである。
That is, in the case of this example, the foaming accelerator 7 has T of the amine 1.
Modified M in which DA is an incyanate component of a resin molding material
It reacts with DI to produce a polymeric compound having a urea bond, and the amine 2, TEDA, acts as a catalyst for this reaction. This reaction is fast and generates a large amount of heat, and in the thick internal molding section 6, the temperature of the resin molding material is made higher than the boiling point of the high boiling point blowing agent.

第3図は、成形型5に射出された樹脂成形材料の内部温
度の経時変化を示すものであって、図中の特性線Aが厚
肉部成形部6での内部温度変化を示し、特性線Bが薄肉
部成形部8での内部温度変化を示す。なお、樹脂成形品
1の薄肉部3の板厚は3.8+aロである。また、この
場合の樹脂成形材料の硬化時間は20〜30秒である。
FIG. 3 shows the change over time in the internal temperature of the resin molding material injected into the mold 5, and the characteristic line A in the figure shows the internal temperature change in the thick-walled molded part 6. Line B shows the internal temperature change in the thin-walled portion 8. Note that the thickness of the thin wall portion 3 of the resin molded product 1 is 3.8+a. Further, the curing time of the resin molding material in this case is 20 to 30 seconds.

第3図から、発泡促進剤7を塗布した厚肉部成形部6で
は樹脂成形材料の温度が射出から5〜9秒間に高沸点発
泡剤の沸点(148.2℃)を越え、この間で高沸点発
泡剤による発泡が進行することがわかる。
From Fig. 3, the temperature of the resin molding material exceeds the boiling point (148.2°C) of the high-boiling point foaming agent in 5 to 9 seconds after injection in the thick-walled molded part 6 coated with the foaming accelerator 7, and during this period It can be seen that foaming by the boiling point foaming agent progresses.

一方、発泡促進剤を塗布していない薄肉部成形部8では
樹脂成形材料の内部温度は上記高沸点発泡剤の沸点まで
は上昇せず、この薄肉部成形部8では高沸点発泡剤は樹
脂成形材料の発泡に寄与しないことがわかる。
On the other hand, the internal temperature of the resin molding material does not rise to the boiling point of the high-boiling point foaming agent in the thin-walled portion molding section 8 to which no foaming accelerator is applied. It can be seen that this does not contribute to foaming of the material.

従って、上記厚肉部成形部6では高沸点発泡剤が樹脂成
形材料の発泡に寄与することにより、その周辺部(薄肉
部成形部8)よりも樹脂成形材料の発泡率が高くなるも
のである。つまり、発泡率が高いということは、樹脂成
形品1はこの厚肉部2においては気孔部が多く、樹脂部
が少ないということであり、この樹脂部が少なくなる分
、収縮率が低くなり、厚肉部2と薄肉部3との収縮量の
差が小さくなるものである。よって、樹脂成形品1にお
ける上記厚肉部2の反対側の面(裏面)1aにヒケを生
ずることが防止される。
Therefore, the high boiling point foaming agent contributes to the foaming of the resin molding material in the thick-walled molded section 6, so that the foaming rate of the resin molded material is higher than that in the surrounding area (thin-walled molded section 8). . In other words, a high foaming rate means that the resin molded product 1 has many pores and few resin parts in the thick part 2, and as the resin part decreases, the shrinkage rate decreases. The difference in the amount of shrinkage between the thick portion 2 and the thin portion 3 is reduced. Therefore, sink marks are prevented from occurring on the surface (back surface) 1a of the resin molded product 1 opposite to the thick portion 2.

実施例の射出成形方法は以上の通りであり、この方法に
より樹脂成形品40本を得たところ、ヒケ不良の発生本
数は1本であった。一方、上記高沸点発泡剤及び発泡促
進剤を利用しない従来の方法の場合、樹脂成形品40本
中でヒケ不良の発生本数が6本であった。
The injection molding method of the example is as described above, and when 40 resin molded products were obtained by this method, the number of sink mark defects was one. On the other hand, in the case of the conventional method that does not use the above-mentioned high-boiling point foaming agent and foaming accelerator, the number of sink mark defects occurred in 6 out of 40 resin molded products.

なお、厚肉部成形部に塗布する発泡促進剤のアミン1と
しては、上記TDA以外にDETDA(ジエチルトルエ
ンジアミン)を用いることもでき、要は成形型の型温度
(70℃前後)以上の沸点を有し、樹脂成形材料のイソ
シアネート成分と反応して樹脂成形材料を局部的に高沸
点発泡剤の沸点以上に昇温せしめるものであればよい。
In addition to the TDA mentioned above, DETDA (diethyltoluene diamine) can also be used as the amine 1 of the foaming accelerator applied to the thick-walled molded part. Any foaming agent may be used as long as it has the following properties and reacts with the isocyanate component of the resin molding material to locally raise the temperature of the resin molding material to a temperature higher than the boiling point of the high boiling point blowing agent.

また、発泡促進剤の塗布にあたっては、離型剤中に混入
してこの離型剤と共にスプレー等によって行なうことも
できる。
Further, when applying the foaming accelerator, it can be mixed into a mold release agent and applied by spraying or the like together with the mold release agent.

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

図面は本発明の実施例を示し、第1図は樹脂成形品の一
部を示す断面図、第2図は成形型の一部を示す断面図、
第3図は成形型5に射出された樹脂成形材料の内部温度
の経時変化を示す特性図である。 1・・・・・・樹脂成形品 2・・・・・・厚肉部 3・・・・・・薄肉部 5・・・・・・成形型 6・・・・・・厚肉部成形部 7・・・・・・発泡促進剤 8・・・・・・薄肉部成形部
The drawings show embodiments of the present invention, FIG. 1 is a sectional view showing a part of a resin molded product, FIG. 2 is a sectional view showing a part of a mold,
FIG. 3 is a characteristic diagram showing the change in internal temperature of the resin molding material injected into the mold 5 over time. 1...Resin molded product 2...Thick wall part 3...Thin wall part 5...Molding mold 6...Thick wall part molding part 7... Foaming accelerator 8... Thin wall portion molding part

Claims (1)

【特許請求の範囲】[Claims] (1)ウレタン、ウレア系樹脂成形材料により厚肉部を
有する樹脂成形品を得る反応射出成形方法であって、 上記樹脂成形材料中にその反応成形温度よりも沸点が高
い高沸点発泡剤を混入しておく一方、成形型における上
記厚肉部を成形する部分に、上記樹脂成形材料中のイソ
シアネート成分と反応し且つその反応による発熱温度が
上記高沸点発泡剤の沸点よりも高いアミン系発泡促進剤
を塗布しておいて、 上記樹脂成形材料を成形型に射出する、 ことを特徴とする反応射出成形方法。
(1) A reaction injection molding method for obtaining a resin molded product having a thick wall part using a urethane or urea resin molding material, wherein a high boiling point blowing agent having a boiling point higher than the reaction molding temperature of the resin molding material is mixed into the resin molding material. On the other hand, an amine-based foaming promoter that reacts with the isocyanate component in the resin molding material and whose exothermic temperature due to the reaction is higher than the boiling point of the high-boiling blowing agent is added to the part of the mold where the thick-walled part is to be molded. A reaction injection molding method comprising: coating a resin molding agent on the resin molding material, and then injecting the resin molding material into a mold.
JP11814989A 1989-05-11 1989-05-11 Reaction injection molding method Pending JPH02295710A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11814989A JPH02295710A (en) 1989-05-11 1989-05-11 Reaction injection molding method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11814989A JPH02295710A (en) 1989-05-11 1989-05-11 Reaction injection molding method

Publications (1)

Publication Number Publication Date
JPH02295710A true JPH02295710A (en) 1990-12-06

Family

ID=14729299

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11814989A Pending JPH02295710A (en) 1989-05-11 1989-05-11 Reaction injection molding method

Country Status (1)

Country Link
JP (1) JPH02295710A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008254332A (en) * 2007-04-05 2008-10-23 Nissan Motor Co Ltd Skin material, its production method and skin material for automobile interior

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008254332A (en) * 2007-04-05 2008-10-23 Nissan Motor Co Ltd Skin material, its production method and skin material for automobile interior

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