JPS6018334A - Surface curing method of resin molded article - Google Patents

Surface curing method of resin molded article

Info

Publication number
JPS6018334A
JPS6018334A JP12640683A JP12640683A JPS6018334A JP S6018334 A JPS6018334 A JP S6018334A JP 12640683 A JP12640683 A JP 12640683A JP 12640683 A JP12640683 A JP 12640683A JP S6018334 A JPS6018334 A JP S6018334A
Authority
JP
Japan
Prior art keywords
temperature
molded article
resin molded
polypropylene
resin
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
JP12640683A
Other languages
Japanese (ja)
Inventor
Yasutomo Funakoshi
康友 船越
Yorihisa Maeda
前田 順久
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP12640683A priority Critical patent/JPS6018334A/en
Publication of JPS6018334A publication Critical patent/JPS6018334A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C71/00After-treatment of articles without altering their shape; Apparatus therefor
    • B29C71/0063After-treatment of articles without altering their shape; Apparatus therefor for changing crystallisation

Abstract

PURPOSE:To improve resistance to flaw and a quality level, by applying specific heat treatment to a resin molded material made from polypropylene or propylene-ethylene copolymer and a nucleating agent. CONSTITUTION:A resin molded article obtained by making use of a resin composite made from a polypropylene or propylene-ethylene copolymer and a nucleating agent is inserted into a furnace whose temperature is higher by 5-10 deg.C than that of crystallization of a material, which has been evaluated beforehand, and left for a predetermined period of time as it is. Then a temperature in the furnace is lowered at a predetermined rate, and surface hardness is raised by making crystallinity of a skin layer of the surface of the molded article improve more than the other part. As heat treatment is applied to polymer containing the uncleating agent like this, a crystal of the polymer of that part is turned into fine, dense and uniform structure and a non-crystalline part becomes smaller, it seems that hardness of the part is improved.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は樹脂成形品の表面層の結晶化度を熱処理により
」二昇さぜ耐傷性の向上および品位向上をd2かる樹脂
成形品の表向硬化方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is directed to surface hardening of resin molded products in which the degree of crystallinity of the surface layer of resin molded products is improved by heat treatment, which improves the scratch resistance and quality of the resin molded products. It is about the method.

従来例の構成とその問題点 一般に樹脂材料は他材料に比べ耐傷性は決して優れてい
るとはいえず、特にその中でオレフィン系の成形材料は
耐傷性については佃脂材料の中では低位のものである。
Structures of conventional examples and their problems In general, resin materials cannot be said to have superior scratch resistance compared to other materials, and olefin-based molding materials in particular have a lower scratch resistance than other Tsukuda resin materials. It is something.

しかし、石油価格の高騰につれて、安価なオレフィン系
材料は多く用いられるに至ったが、耐傷性が悪く広く外
装用途に用いられてないのが現状である。そこで、この
傷が伺きにくくするため、製品の設計面からガードを設
ける、艶消し皮シボを施こす等の工夫をこらし、又、材
料面からは、充填剤、ポリマー等の工夫か種々検討され
ているが、現在外装用途に最も適した方法がないのが現
状である。そのだめ、一般には外装用にはオレフィン系
と比ベコスト高のスチロール系の材料が用いられている
のである。このように、オレフィン系材料が外装用とし
て広く実用に供されないのは耐傷性に大きな問題がある
だめである。
However, as petroleum prices have soared, many inexpensive olefin-based materials have come into use, but they currently have poor scratch resistance and are not widely used for exterior applications. Therefore, in order to make these scratches difficult to see, we have taken measures such as providing a guard and applying matte skin texture from the product design perspective.In addition, from the material perspective, we have considered various methods such as fillers, polymers, etc. However, there is currently no method that is most suitable for exterior applications. As a result, styrene-based materials, which are more expensive than olefin-based materials, are generally used for exterior materials. As described above, the reason why olefin-based materials are not widely put into practical use for exterior packaging is that they have serious problems with scratch resistance.

発明の目的 本発明は従来のこのような欠点を除去するものであり、
その方法はオレフィン系のような安価な結晶性材料にお
いて、所定の結晶化制御材料を所定量含む成形材料を用
いた成形品に熱処理を施こすことによりその製品の表面
層の結晶化度を上昇させて、耐傷性を向上させる方法を
提供するものである。
OBJECTS OF THE INVENTION The present invention obviates these drawbacks of the prior art.
The method is to increase the degree of crystallinity of the surface layer of an inexpensive crystalline material such as an olefin by heat-treating the molded product using a molding material containing a predetermined amount of a specific crystallization control material. The present invention provides a method for improving scratch resistance.

発明の構成 本発明の樹脂成形品の表面硬化方法は温度が所定速度が
降温可能な炉体を有する装置を使用し、所定の結晶化制
御材料を所定量含むオレフィン系材料で成形された成形
品をあらかじめ評価しておいたその材料の結晶化温度よ
り5〜1o′C高い炉内に挿入し、一定の時間放置する
、その後、この炉内の温度を一定の速度で降温し、成形
品表面のスキン層の結晶化度を他の部分より上昇させて
、表面硬度を上げるものである。
Components of the Invention The method for surface curing resin molded articles of the present invention uses an apparatus having a furnace body capable of lowering the temperature at a predetermined rate, and cures molded articles made of an olefin material containing a predetermined amount of a predetermined crystallization control material. is inserted into a furnace that is 5 to 1 o'C higher than the pre-evaluated crystallization temperature of the material, and left for a certain period of time.Then, the temperature inside this furnace is lowered at a certain rate, and the surface of the molded product is The crystallinity of the skin layer is increased compared to other parts, thereby increasing the surface hardness.

実施例の説明 以下に本発明の実施例を具体的に説明する。Description of examples Examples of the present invention will be specifically described below.

実施例 1 M、I(メルトフローインデックス)〜16のホモポリ
プロピレンに安息香酸アルミニウム0.2wt%、ジベ
ンジリデンソルビトール0.1wt%ヲ加え高速混合機
にて混合攪拌後、φ30の異方向ベント型押出し機にて
ペレット化し80″Cで乾燥後、このペレットを成形機
に投入、樹脂温度1800〜230°C1金型温度30
〜40′Cでφ50X10tの製品の成形を行ない成形
品を得た。この成形品の結晶化温度を熱分析法で測定す
ると135°Cであった。そこで、炉の温度を約140
〜146°Cに設定し、この炉内に上記成形品を挿入し
、約30分間放置後2°C/10で40°Cまで降温し
表面層に熱処理を施こし硬化層を形成した。こり表面層
部分の結晶化度を水−エタノール系密度勾配管法で密度
測定を行ない、その後結晶化度換算すると熱処理前の6
5〜70に対し76〜85であった。このようにして得
た試料を鉛筆硬度試験法で測定すると表−1に示す結果
であった。
Example 1 0.2 wt% of aluminum benzoate and 0.1 wt% of dibenzylidene sorbitol were added to homopolypropylene with M, I (melt flow index) ~16, mixed and stirred in a high-speed mixer, and then extruded in a φ30 different direction vent type. After pelletizing in a machine and drying at 80"C, put the pellets into a molding machine, resin temperature 1800-230°C 1 mold temperature 30
A product of φ50×10t was molded at ~40'C to obtain a molded product. The crystallization temperature of this molded article was determined to be 135°C by thermal analysis. Therefore, the temperature of the furnace was set to about 140
The temperature was set at ~146°C, the molded article was inserted into this furnace, and after being left for about 30 minutes, the temperature was lowered to 40°C at a rate of 2°C/10, and the surface layer was heat-treated to form a hardened layer. The crystallinity of the surface layer of the lump was measured using a water-ethanol density gradient tube method, and the crystallinity was then converted to 6
It was 76-85 compared to 5-70. When the sample thus obtained was measured using a pencil hardness test method, the results were shown in Table 1.

実施例−2 実施例−1で用いたものと同じホモボリフ゛口ビレン(
造核剤を含まない)を用い樹脂温度1800〜230℃
、金型温度30〜40°Cでφ5Q×10tの製品の成
形を行ない成形品を得た。この成形汚^を実施例−1と
同じ方法で熱処理を施こし試料を得た。この試料の結晶
化度は60〜66であり硬度測定の結果を表−1にボす
Example-2 The same homobolyphic virens used in Example-1 (
(does not contain nucleating agent) resin temperature 1800-230℃
A product of φ5Q×10t was molded at a mold temperature of 30 to 40°C to obtain a molded product. This molded stain was heat treated in the same manner as in Example-1 to obtain a sample. The crystallinity of this sample was 60 to 66, and the hardness measurement results are shown in Table 1.

実施例−3 実施例−1で得た成形品を約140〜145°Cの炉内
に挿入し約30分間放置後120〜130°Cで30分
間、次に110〜120”Cで30分間、次に90℃〜
100°Cで30分間、次に70〜8Q°Cで30分間
、次に50〜60°Cで30分間放置し成形品表面に硬
化層を形成した。このようにして得た試料を鉛筆硬度試
験法で測定すると表−1に示す結果であった。
Example-3 The molded product obtained in Example-1 was placed in a furnace at about 140-145°C, left for about 30 minutes, then heated at 120-130°C for 30 minutes, then at 110-120"C for 30 minutes. , then 90℃~
A hardened layer was formed on the surface of the molded product by standing at 100°C for 30 minutes, then at 70-8Q°C for 30 minutes, and then at 50-60°C for 30 minutes. When the sample thus obtained was measured using a pencil hardness test method, the results were shown in Table 1.

実施例−4 実施例−1で得た成形品を約140〜146°Cの炉内
に挿入し約30分間放置後100°Ctでは0.5°C
/分の速度で降温し、更に60°Cまでは6°C/分の
速度で降温し成形′島表面に硬化層を形成した。このよ
うにして得た試料を鉛筆硬度試験法で測定すると表−1
に示す結果であった。
Example-4 The molded product obtained in Example-1 was inserted into a furnace at about 140 to 146°C, and after being left for about 30 minutes, the temperature at 100°Ct was 0.5°C.
The temperature was lowered at a rate of 6°C/min until it reached 60°C, and a hardened layer was formed on the surface of the molded island. The samples obtained in this way were measured using the pencil hardness test method and Table 1
The results are shown in.

実施例−9 M、l−24のABS樹脂を用い樹脂温度230’C〜
240°C金型温度40〜6o℃でφ50X10tの製
品の成形を行ない成形品を得た。この試料の硬度測定の
結果を表−1に示す。
Example-9 Using M, l-24 ABS resin, resin temperature 230'C~
A product of φ50×10t was molded at 240° C. and a mold temperature of 40 to 60° C. to obtain a molded product. Table 1 shows the results of hardness measurement of this sample.

実施例6〜8 M 、I=20のエチレン−プロピレンブロック共重合
体を用い実施例−1,2,3及び4と同様の方法で表面
硬化処理を行ない表面に硬化層を形成した。このように
して得た試料を鉛筆硬度試験法で測定すると表−1に示
す結果であった。
Examples 6 to 8 Using an ethylene-propylene block copolymer of M and I=20, a surface hardening treatment was performed in the same manner as in Examples 1, 2, 3, and 4 to form a hardened layer on the surface. When the sample thus obtained was measured using a pencil hardness test method, the results were shown in Table 1.

参考例−1,2 M、I=−1sのホモポリプロピレン及びM、I=20
(D−r−fVノープロピレンブロソク共重合体の硬度
、結晶化度測定結果を表−1に示す。
Reference Example-1, 2 Homopolypropylene with M, I=-1s and M, I=20
(Table 1 shows the hardness and crystallinity measurement results of the D-r-fV no-propylene broth copolymer.

以 下 余 白 表 −1 シ ? ( 発明の効果 以上、説明したように結晶性ポリマー、特にポリプロピ
レンにおいてはポリマー中に造核効果を有する物質を添
加することにより未添加ポリマーと比べ結晶化度は約8
%向上する。更にこのポリマーの結晶化温度以上の温度
で加熱処理することでよりその表面部分の結晶化度が更
に約20%向上し、このポリプロピレンの耐傷性はAB
Sとは・丁同様のものになることが明らかになった。
Below is the margin table -1? (As explained above, in crystalline polymers, especially polypropylene, by adding a substance that has a nucleating effect to the polymer, the degree of crystallinity can be reduced to about 8.
%improves. Furthermore, by heat treatment at a temperature higher than the crystallization temperature of this polymer, the crystallinity of the surface area is further improved by about 20%, and the scratch resistance of this polypropylene is AB
It has become clear that S is the same as Ding.

このように造核剤を含むポリマーに熱処理を施こすこと
によりその部分のポリマーの結晶は微細で微密で均質な
構造をとり、更に非結晶性部分が小さくなることにより
その部分の硬度が向上するもつと思われる。なお、この
本文中ではポリプロピレンとしてはホモポリマーグレー
ドを用いたがコポリマーブレードでも同様の効果を得る
ことが出東るものである。
By heat-treating a polymer containing a nucleating agent in this way, the polymer crystals in that area become fine, minutely dense, and homogeneous, and the amorphous area becomes smaller, improving the hardness of that area. It seems to be the case. In this text, a homopolymer grade polypropylene is used as the polypropylene, but the same effect can be obtained with a copolymer braid.

代理人の氏名 弁理士 中 尾 敏 男 ほか1名−1
75’)−
Name of agent: Patent attorney Toshio Nakao and 1 other person-1
75')-

Claims (1)

【特許請求の範囲】[Claims] ポリプロピレンまたハ、プロピレン−エチレン共重合体
のいづれかと造核剤とから成る樹脂組成物を用いた樹脂
成形品を、前記樹脂組成物が示す結晶化温度以上の温度
で加熱した後、所定の速度で降温し成形品表面層の結晶
化度を上昇させる樹脂成形品の表面硬化方法。
After heating a resin molded article using a resin composition comprising either polypropylene or propylene-ethylene copolymer and a nucleating agent at a temperature equal to or higher than the crystallization temperature of the resin composition, it is heated at a predetermined rate. A surface hardening method for resin molded products in which the temperature is lowered to increase the degree of crystallinity of the surface layer of the molded product.
JP12640683A 1983-07-11 1983-07-11 Surface curing method of resin molded article Pending JPS6018334A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12640683A JPS6018334A (en) 1983-07-11 1983-07-11 Surface curing method of resin molded article

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12640683A JPS6018334A (en) 1983-07-11 1983-07-11 Surface curing method of resin molded article

Publications (1)

Publication Number Publication Date
JPS6018334A true JPS6018334A (en) 1985-01-30

Family

ID=14934364

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12640683A Pending JPS6018334A (en) 1983-07-11 1983-07-11 Surface curing method of resin molded article

Country Status (1)

Country Link
JP (1) JPS6018334A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62256803A (en) * 1986-04-30 1987-11-09 Idemitsu Petrochem Co Ltd Propylene homopolymer and its production
JPS62256837A (en) * 1986-04-30 1987-11-09 Idemitsu Petrochem Co Ltd Production of polypropylene resin molding
US5288450A (en) * 1991-02-27 1994-02-22 Toyoda Gosei Co., Ltd. Process for producing molded article of continuous length
US5489404A (en) * 1994-08-08 1996-02-06 General Electric Company Process for annealing thermoplastics
US6423263B1 (en) * 1997-02-25 2002-07-23 Toyoda Gosei Co., Ltd. Method for producing molded crystalline resin article

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62256803A (en) * 1986-04-30 1987-11-09 Idemitsu Petrochem Co Ltd Propylene homopolymer and its production
JPS62256837A (en) * 1986-04-30 1987-11-09 Idemitsu Petrochem Co Ltd Production of polypropylene resin molding
US5288450A (en) * 1991-02-27 1994-02-22 Toyoda Gosei Co., Ltd. Process for producing molded article of continuous length
US5489404A (en) * 1994-08-08 1996-02-06 General Electric Company Process for annealing thermoplastics
US6423263B1 (en) * 1997-02-25 2002-07-23 Toyoda Gosei Co., Ltd. Method for producing molded crystalline resin article

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