JPS59201832A - Preparation of injection molded article - Google Patents
Preparation of injection molded articleInfo
- Publication number
- JPS59201832A JPS59201832A JP7668683A JP7668683A JPS59201832A JP S59201832 A JPS59201832 A JP S59201832A JP 7668683 A JP7668683 A JP 7668683A JP 7668683 A JP7668683 A JP 7668683A JP S59201832 A JPS59201832 A JP S59201832A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- injection molding
- injection molded
- molded product
- injection
- 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
Links
- 238000002347 injection Methods 0.000 title claims description 15
- 239000007924 injection Substances 0.000 title claims description 15
- 238000001746 injection moulding Methods 0.000 claims abstract description 16
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 16
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 10
- 239000000178 monomer Substances 0.000 claims abstract description 8
- 239000002966 varnish Substances 0.000 claims abstract description 8
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 150000008360 acrylonitriles Chemical class 0.000 claims 1
- -1 aromatic vinyl compound Chemical class 0.000 abstract description 8
- 229920002554 vinyl polymer Polymers 0.000 abstract description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 1
- 229920000058 polyacrylate Polymers 0.000 abstract 1
- 238000000465 moulding Methods 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 7
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 238000007747 plating Methods 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- 239000005062 Polybutadiene Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- SQHOHKQMTHROSF-UHFFFAOYSA-N but-1-en-2-ylbenzene Chemical compound CCC(=C)C1=CC=CC=C1 SQHOHKQMTHROSF-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/17—Component parts, details or accessories; Auxiliary operations
- B29C45/26—Moulds
- B29C45/37—Mould cavity walls, i.e. the inner surface forming the mould cavity, e.g. linings
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は1表面光沢がすぐれ、光沢むらのない射出成形
品の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an injection molded article with excellent surface gloss and no uneven gloss.
従来、オレフィン系、スチレン系等の熱可塑性樹脂の射
出成形に際しては、射出成形品の表面光沢を向上させる
ため金型のキャビティー面を硬質クロムメッキ等の表面
処理が行なわれている。しかし、従来の金属メッキ法で
は、成形材料によっては十分な光沢が得られない場合も
多く見られている。このため、成形条件、とくに金型温
度を高くして光沢全向上する方法が用いられているが。Conventionally, when injection molding thermoplastic resins such as olefin and styrene, the cavity surface of the mold is subjected to surface treatment such as hard chrome plating in order to improve the surface gloss of the injection molded product. However, with conventional metal plating methods, it is often the case that sufficient gloss cannot be obtained depending on the molding material. For this reason, methods are used to improve the overall gloss by increasing the molding conditions, especially the mold temperature.
金型温度を高くすると成形時間が長くなり生産性が著し
く低下したり、成形品の形状によっては成形品表面に陥
没部が生ずるいわゆるヒケ現象が発生し易くなることか
ら実用的には限定された方法にすぎない。他方、デザイ
ン上の必要性から成形品面にシボ模様を有する成形品も
多くの場合に用いられているが、従来の金属メッキ処理
ではシボ模様を有する場合にはシボ面のゲート部、ウェ
ルドライン部で光沢むらが生じやすく成形外観が著しく
損わn、従来の金属メッキ処理、成形条件等の改良では
この光沢むらを解決し得なかった。If the mold temperature is raised, the molding time becomes longer, which significantly reduces productivity, and depending on the shape of the molded product, the so-called sink mark phenomenon, which causes depressions on the surface of the molded product, is more likely to occur, so its practical use is limited. It's just a method. On the other hand, molded products with a textured pattern on the surface of the molded product are often used due to design needs, but in conventional metal plating processes, when the textured pattern is present, the gate area and weld line of the textured surface are The unevenness of gloss tends to occur in some areas, which seriously impairs the appearance of the molded product.This unevenness of gloss cannot be solved by conventional metal plating treatment, improvement of molding conditions, etc.
なお、従来一般に、金型面にオイル状またはエマルショ
アタイプのシリコーン離型剤(非硬化性)を塗布する方
法が用いられているが、これは、成形に際して、樹脂が
金型に膠着するのを防ぎ、成形品を取出しやすくするも
のであり、成形品の外観を向上させる効果はない。Conventionally, a method of applying an oil-type or emulsion-type silicone mold release agent (non-curing) to the mold surface has been used, but this method prevents the resin from sticking to the mold during molding. This prevents molding from occurring and makes it easier to take out the molded product, but it does not have the effect of improving the appearance of the molded product.
本発明は、このような間粗点を解決するものである。The present invention solves this problem.
すなわち9本発明は、熱可塑性樹脂の射出成形において
、金型のキャビディ而が厚さ5〜100μmのシリコー
ンフェスの硬化被覆膜で被覆されている金型を用いて射
出成形することを特徴とする射出成形品の製造方法に関
する。That is, the present invention is characterized in that, in injection molding of thermoplastic resin, the injection molding is carried out using a mold in which the cavity of the mold is coated with a cured coating film of silicone face having a thickness of 5 to 100 μm. The present invention relates to a method for manufacturing injection molded products.
本発明の熱可塑性樹脂としては、ラジカル共重合によっ
て得られる重合体がある。このうち、オvフィン系の熱
可塑性樹脂としては、ポリエチレン、ポリプロピレン、
エチレン−プロピレン共重合体、エチレン−プロピレン
−ジエン共重合体。The thermoplastic resin of the present invention includes a polymer obtained by radical copolymerization. Among these, ov-fin type thermoplastic resins include polyethylene, polypropylene,
Ethylene-propylene copolymer, ethylene-propylene-diene copolymer.
ポリブタジェン等がある。また、スチレン系の熱可塑性
樹脂としては、スナレン、クロロスチレン。Examples include polybutadiene. In addition, examples of styrene-based thermoplastic resins include sunalene and chlorostyrene.
ビニルトルエン、α−メチルスチレン、α−エチルスチ
レン等のスチレン系モノマーの重合体または共重合体、
スチレン系モノマーとアクリロニトリル、メタクリル酸
アルキルエステル等の他のモノマーとの共重合体(例え
ばスチレン−アクリロニトリル共重合体)、ポリブタジ
ェン、エチレン−フロピレン共i合体、エチレン−プロ
ピレン−ジエン共重合体、アクリル酸アルキルエステル
重合体等のゴム成分にスチレン系モノマーおよび必要に
応じ他のモノマーをグラフト重合させて得られるもの(
例えば、アクリロニトリル−ポリブタジェンコム−スチ
レン三元共重合体、アクリロニトリル−アクリル酸アル
キルエステル重合体−スチレン共重合体等)がある。な
お、ここで、アクリル酸アルキルエステル重合体とは、
アクリル酸ブチル等のアクリル鍍アルキルエステルを必
要に応じ、ジビニルベンゼン、エチレングリコールジメ
タクリレート、トリアリルインシアヌレート。Polymers or copolymers of styrenic monomers such as vinyltoluene, α-methylstyrene, α-ethylstyrene, etc.
Copolymers of styrene monomers with other monomers such as acrylonitrile and methacrylic acid alkyl esters (e.g. styrene-acrylonitrile copolymers), polybutadiene, ethylene-propylene copolymer, ethylene-propylene-diene copolymer, acrylic acid Products obtained by graft polymerizing a styrene monomer and other monomers as necessary to a rubber component such as an alkyl ester polymer (
Examples include acrylonitrile-polybutadiene comb-styrene terpolymer, acrylonitrile-acrylic acid alkyl ester polymer-styrene copolymer, etc. In addition, here, the acrylic acid alkyl ester polymer is
If necessary, add acrylic alkyl esters such as butyl acrylate, divinylbenzene, ethylene glycol dimethacrylate, triallyl in cyanurate.
トリアリルシアヌレート、トリス(2−アクリロイルオ
キシエチル)インシアヌレート等の多官能性モノマーお
よび必要に応じポリブタジェンゴムの存在下重合させて
得られるものでるる。−また。It is obtained by polymerization in the presence of a polyfunctional monomer such as triallyl cyanurate or tris(2-acryloyloxyethyl)in cyanurate and, if necessary, polybutadiene rubber. -Again.
アクリル酸アルキルエステル重合体はベンゾイルパーオ
キサイド等の過酸化物で架橋させたものでもよい。The acrylic acid alkyl ester polymer may be crosslinked with a peroxide such as benzoyl peroxide.
本発明の熱可塑性樹脂としては、上記アクリル酸アルキ
ルエステル重合体にスチレン系モノマー等の芳合族ビニ
ル化合物、アクリロニトリル等のビニルシアン化合物お
よびメタクリル酸メチル等のメタクリル酸アルキルエス
テルのうち、少なくとも一種以上、特に好ましくは、ス
チレン系モノマーを含む少なくとも二種以上のモノマー
を重合させて得られるものが1表面光沢および光沢むら
のない射出成形品を得るという点で改善効果が優れる。The thermoplastic resin of the present invention includes at least one selected from the above-mentioned acrylic acid alkyl ester polymer, an aromatic vinyl compound such as a styrene monomer, a vinyl cyanide compound such as acrylonitrile, and a methacrylic acid alkyl ester such as methyl methacrylate. Particularly preferably, a product obtained by polymerizing at least two or more monomers including a styrene monomer has an excellent improvement effect in that an injection molded product with no surface gloss and no uneven gloss can be obtained.
なお1本発明の熱可塑性樹脂は、上記したもの全二種以
上ブレンドしたものでもよい。Note that the thermoplastic resin of the present invention may be a blend of two or more of the above-mentioned resins.
本発明におけるシリコーンフェスとしては、メチルンリ
コーンヮニス、メチルフェニルンリコーンワニス等の末
端にシラノール基を含み、触媒の存在ドまたは不存在下
に常温または加熱下に架橋反応し、三次元構造の硬化物
となるものが使用される。The silicone varnish in the present invention includes a silanol group at the end of methyl silicone varnish, methyl phenyl silicone varnish, etc., which undergoes a crosslinking reaction at room temperature or under heating in the presence or absence of a catalyst, resulting in a three-dimensional structure. A cured product is used.
金型のキャビティー面にシリコーンワニスノ硬化被膜を
形成するには、まず、金型のキャビティーにシリコーン
フェスをノーヶ塗り、スプレー塗装等の方法に塗装し、
常温でまたは加熱して硬化させられる。このときの好ま
しい硬化条件は、シリコーンフェスの種類によって異な
るが1通常、100〜250℃に加熱して硬化させるの
〃二、硬化被膜の金型面への密着度1表面硬度を向上さ
せ、射出成形品の光沢を向上させる上で好ましい。To form a hardened silicone varnish film on the cavity surface of the mold, first, coat the cavity of the mold with silicone varnish, spray paint, etc.
It can be cured at room temperature or by heating. The preferred curing conditions at this time vary depending on the type of silicone face, but 1. Usually, it is cured by heating to 100 to 250°C. 2. It improves the adhesion of the cured film to the mold surface, 1. It improves the surface hardness, and This is preferable for improving the gloss of molded products.
硬化被膜の厚さは、5〜100μm、好ましくは10〜
5 Q ltmにされる。5μm未満では、光沢向上効
果が低くなり、100μmを越えると射出成形後の冷却
工程が長くなり、成形サイクルが長くなる。The thickness of the cured film is 5 to 100 μm, preferably 10 to 100 μm.
5 Q It is made ltm. If it is less than 5 μm, the gloss improvement effect will be low, and if it exceeds 100 μm, the cooling process after injection molding will be long, resulting in a longer molding cycle.
本発明で、射出成形するに際しての射出成形機。An injection molding machine for injection molding according to the present invention.
射出成形条件については制約はなく、成形材料。There are no restrictions on injection molding conditions and molding materials.
成形品の形状等から選定されるべきものである。It should be selected based on the shape of the molded product, etc.
例えば、射出成形機としては9通常のスクリュ一式また
はプランジャ一式射出成形機が使用できる。廿た。成形
温度は樹脂の溶融温度から決められるが、樹脂がシリン
ダー内で充分溶融される温度でかつ熱分解等によシ劣化
しない温度に設定される。射出圧力は、成形温度から決
められるが。For example, as the injection molding machine, a conventional one-screw or one-plunger injection molding machine can be used. It was a long time ago. The molding temperature is determined by the melting temperature of the resin, and is set at a temperature at which the resin is sufficiently melted within the cylinder and at which it does not deteriorate due to thermal decomposition or the like. The injection pressure is determined by the molding temperature.
ショートショット及びヒケが生じないために必要な圧力
以上で、パリが生じない圧力以下に設定される。金型温
度は、一般に20〜100℃であるが、樹脂の流れ性、
成形温度、肉厚、成形サイクル等の条件から適宜選定さ
れる。The pressure is set above the pressure necessary to prevent short shots and sink marks, and below the pressure that does not cause flash. The mold temperature is generally 20 to 100°C, but depending on the flowability of the resin,
It is selected as appropriate based on conditions such as molding temperature, wall thickness, and molding cycle.
次[実施例を示す。Next [Example is shown]
実施例1
金型のキャビティー面をシリコーンフェス(50チトル
工ン溶iM、)−レ・シリコーンSR,2410゜トー
ン・シリコーン■商品名)をスプレー塗布し。Example 1 The cavity surface of the mold was spray coated with silicone face (50 Tittle Melt iM) - Re Silicone SR, 2410° Tone Silicone (trade name).
200℃で30分間焼付して30μmの硬化被膜を形成
した。この金型を用いて射出成形機(日鋼アンケルベル
グ■製V36A−450型)で、樹脂温度240℃、金
型温度50°C1射田圧力500に97cm2の成形条
件でアクリロニトリル−アクリル酸アルキルエステル重
合体−スチレン共重合体(パイタックスV6700.日
立化成工業■商品名)を射出成形した。It was baked at 200° C. for 30 minutes to form a hardened film of 30 μm. Using this mold, an acrylonitrile-acrylic acid alkyl ester polymer was molded using an injection molding machine (model V36A-450 manufactured by Nikko Ankelberg ■) under the following conditions: resin temperature 240°C, mold temperature 50°C, injection field pressure 500, and 97cm2. A polymerized styrene copolymer (Pitax V6700.Hitachi Chemical Co., Ltd. trade name) was injection molded.
成形品の表面の光沢度(反射角60°)をクロスメータ
ーを用いて測定した結果を表IVC示す。また、シリコ
ーンフェスの硬化被膜を形成しなかった金型を用いて同
様に射出成形し、評価した。この結果を表1に示す。Table IVC shows the results of measuring the glossiness (reflection angle of 60°) of the surface of the molded product using a crossmeter. In addition, injection molding was performed in the same manner using a mold in which no cured film of the silicone face was formed, and evaluation was made. The results are shown in Table 1.
表1 測定結果
実施例2
射出成形金型の表面にシボ模様(株式会社棚沢八光社製
のFNDB2及びUNDAx )をほどこした平板金型
にシリコーンフェス(50%トルエン溶液)をスプレー
塗装し、200℃で30分間焼付して、厚さ20μmの
硬化被膜を形成した。この金型を用いて、実施例1と同
じ成形機、成形条件にて射出成形した。Table 1 Measurement Results Example 2 Silicone face (50% toluene solution) was spray-painted on a flat plate mold with a grain pattern (FNDB2 and UNDAx manufactured by Tanazawa Hakkosha Co., Ltd.) on the surface of the injection mold. It was baked at ℃ for 30 minutes to form a hardened film with a thickness of 20 μm. Using this mold, injection molding was carried out using the same molding machine and molding conditions as in Example 1.
この平板は3点のゲー)k有して、ウェルドラインが2
ケ所に発生する構岳となっている。一方かった金型を用
いて、同一材料を同一条件にて射出成形した。射出成形
品の成形外観を評価した結果を表2に示す。This flat plate has a game of 3 points and a weld line of 2
It is a ridge that occurs in several places. On the other hand, the same material was injection molded under the same conditions using a different mold. Table 2 shows the results of evaluating the molded appearance of the injection molded product.
表2 成形外観
そ実施例1と同様
射出成形金型のキャビティー面にシリコーンフェスの硬
化被膜をほどこした金型を用いることにより、射出成形
品の表面光沢を向上させ、またシボ面での光沢むらを消
失させる効果が得られる。Table 2 Molding appearance As in Example 1, by using a mold with a hardened silicone face coating applied to the cavity surface of the injection mold, the surface gloss of the injection molded product was improved, and the gloss on the grained surface was improved. The effect of eliminating unevenness can be obtained.
Claims (1)
ィー面が厚さ5〜100μmのシリコーンワニスの硬化
被覆膜で被覆されている金型を用いて射出成形すること
を特徴とする射出成形品の製造方法。 2、熱可塑性樹脂がアクリル酸アルキルエステル重合体
に芳香族ビニル化合物、ビニルシアン化合物およびメタ
クリル酸アルキルエステルのウチから選ばれた一種以上
の単量体をグラフト重合させて得られるものである特許
請求の範囲第1項記載の射出成形品の製造方法。[Scope of Claims] 1. In injection molding of thermoplastic resin, injection molding is performed using a mold whose cavity surface is coated with a cured coating film of silicone varnish having a thickness of 5 to 100 μm. A method for manufacturing an injection molded product characterized by: 2. A patent claim in which the thermoplastic resin is obtained by graft polymerizing an acrylic acid alkyl ester polymer with one or more monomers selected from aromatic vinyl compounds, vinyl cyanide compounds, and methacrylic acid alkyl esters. A method for producing an injection molded product according to item 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7668683A JPS59201832A (en) | 1983-04-30 | 1983-04-30 | Preparation of injection molded article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7668683A JPS59201832A (en) | 1983-04-30 | 1983-04-30 | Preparation of injection molded article |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS59201832A true JPS59201832A (en) | 1984-11-15 |
Family
ID=13612329
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7668683A Pending JPS59201832A (en) | 1983-04-30 | 1983-04-30 | Preparation of injection molded article |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59201832A (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5748035A (en) * | 1980-09-08 | 1982-03-19 | Okabe Co Ltd | Constructing method for culvert |
-
1983
- 1983-04-30 JP JP7668683A patent/JPS59201832A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5748035A (en) * | 1980-09-08 | 1982-03-19 | Okabe Co Ltd | Constructing method for culvert |
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