JP3163723B2 - Methacrylic resin composition - Google Patents

Methacrylic resin composition

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Publication number
JP3163723B2
JP3163723B2 JP06469792A JP6469792A JP3163723B2 JP 3163723 B2 JP3163723 B2 JP 3163723B2 JP 06469792 A JP06469792 A JP 06469792A JP 6469792 A JP6469792 A JP 6469792A JP 3163723 B2 JP3163723 B2 JP 3163723B2
Authority
JP
Japan
Prior art keywords
fatty acid
carbon atoms
higher fatty
methacrylic resin
weight
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
JP06469792A
Other languages
Japanese (ja)
Other versions
JPH05262950A (en
Inventor
剛 橋本
坂本  隆
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP06469792A priority Critical patent/JP3163723B2/en
Publication of JPH05262950A publication Critical patent/JPH05262950A/en
Application granted granted Critical
Publication of JP3163723B2 publication Critical patent/JP3163723B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、加工性に優れたメタク
リル系樹脂組成物に関するものである。特に、金型を用
いた成形加工時の離型性に優れたメタクリル系樹脂組成
物に関する物である。
The present invention relates to a methacrylic resin composition having excellent processability. In particular, the present invention relates to a methacrylic resin composition having excellent releasability at the time of molding using a mold.

【0002】[0002]

【従来の技術】メタクリル系樹脂は、本来の特性の優れ
た透明性、耐候性、良好な機械的性質を生かして、メー
ターカバー等の自動車部品、光ディスク、レンズ等の光
学部品、電灯カバー等の照明部品等に使用されている。
これらの成形品は一般に射出成形、射出圧縮成形等で得
られているが、光学レンズや光ディスクのような精密金
型成形においては、成形品と金型面との密着性が極めて
高くなるために型離れ不良が発生し、生産性を低下させ
る結果となっている。
2. Description of the Related Art A methacrylic resin is used in automobile parts such as meter covers, optical parts such as optical discs and lenses, and electric light covers, etc. by making use of its original properties of excellent transparency, weather resistance and good mechanical properties. Used for lighting parts.
These molded products are generally obtained by injection molding, injection compression molding, etc., but in precision mold molding such as optical lenses and optical disks, the adhesion between the molded product and the mold surface is extremely high. As a result, mold release failure occurs, resulting in a decrease in productivity.

【0003】そこでメタクリル樹脂に各種離型剤を含有
させることが提案されている。例えば、特開昭61-73754
号公報には、メタクリル系樹脂に、多価アルコール、高
級脂肪酸エステル、高級アルコール、高級脂肪酸、高級
脂肪酸アミド、高級脂肪酸金属塩を添加した樹脂組成物
が提案されている。
[0003] Therefore, it has been proposed that methacrylic resins contain various release agents. For example, JP-A-61-73754
In Japanese Patent Application Publication No. H11-264, a resin composition in which a polyhydric alcohol, a higher fatty acid ester, a higher alcohol, a higher fatty acid, a higher fatty acid amide, and a higher fatty acid metal salt are added to a methacrylic resin is proposed.

【0004】[0004]

【発明が解決しようとする課題】しかしながらこれらの
樹脂組成物での射出成形を行った場合、ある程度の離型
性能は認められるものの未だ充分でない。その上添加さ
れている離型剤やその他の添加剤が樹脂表面に移行し
て、金型表面あるいは成形品表面を汚したり、成形品の
着色をもたらすなど成形品の商品価値を著しく低下させ
る。
However, when injection molding is performed with these resin compositions, a certain degree of mold release performance is recognized, but not yet sufficient. In addition, the added release agent and other additives migrate to the surface of the resin, thereby contaminating the surface of the mold or the surface of the molded product or causing coloring of the molded product, thereby significantly lowering the commercial value of the molded product.

【0005】本発明は、従来の離型剤のもつ欠点を克服
し、より少ない配合量によって優れた離型効果を発揮す
るメタクリル系樹脂組成物を提供する。
The present invention provides a methacrylic resin composition which overcomes the drawbacks of the conventional release agents and exhibits an excellent release effect with a smaller amount.

【0006】[0006]

【課題を解決するための手段】本発明はメタクリル酸メ
チル系重合体100重量部に、下記一般式、
According to the present invention, 100 parts by weight of a methyl methacrylate-based polymer has the following general formula:

【化2】R1COOR2 (式中、R1は炭素数10〜22の脂肪族炭化水素基、
2は炭素数1〜22のアルキル基を示す)で表される
高級脂肪酸エステルと、炭素数10〜22の高級脂肪酸
のグリセリンモノエステルを重量比10/90〜90/
10で、0.02〜0.5重量部、及び必要に応じて紫
外線吸収剤、耐候剤、難燃剤、着色剤、顔料、強化繊維
または無機充填剤を含有し、その他のものを含有しない
メタクリル系樹脂組成物に関するものである。
## STR2 ## R 1 COOR 2 (wherein, R 1 is an aliphatic hydrocarbon group having 10 to 22 carbon atoms,
R 2 represents an alkyl group having 1 to 22 carbon atoms) and a glycerin monoester of a higher fatty acid having 10 to 22 carbon atoms in a weight ratio of 10/90 to 90 /
10, 0.02 to 0.5 parts by weight , and if necessary purple
External absorbent, weathering agent, flame retardant, colorant, pigment, reinforced fiber
The present invention also relates to a methacrylic resin composition containing an inorganic filler and containing no other filler .

【0007】本発明でいうメタクリル酸メチル系重合体
とは、メタクリル酸メチル単独重合体、またはメタクリ
ル酸メチルと20重量%以下のアクリル酸エステルもし
くはメタクリル酸エステル、アクリル酸、メタクリル
酸、スチレン、アクリロニトリルあるいは、ジエン系ゴ
ムやグルタル酸無水物、グルタルイミドなどとの共重合
体をいう。なお、アクリル酸エステルとしてはアクリル
酸メチル、アクリル酸エチル、アクリル酸ブチルなど、
メタクリル酸エステルとしてはメタクリル酸エチル、メ
タクリル酸ブチル、メタクリル酸シクロヘキシルなどで
ある。
The methyl methacrylate polymer referred to in the present invention is a homopolymer of methyl methacrylate or methyl methacrylate and not more than 20% by weight of an acrylate or methacrylate, acrylic acid, methacrylic acid, styrene, acrylonitrile. Alternatively, it refers to a copolymer with a diene rubber, glutaric anhydride, glutarimide, and the like. In addition, as the acrylate, methyl acrylate, ethyl acrylate, butyl acrylate, etc.
Examples of the methacrylate include ethyl methacrylate, butyl methacrylate, and cyclohexyl methacrylate.

【0008】本発明の前記一般式で表される高級脂肪酸
エステルとしては、例えばラウリン酸のメチル,エチ
ル,プロピル,ブチルの各エステル、パルミチン酸のメ
チル,エチル,プロピル,ブチルの各エステル、ステア
リン酸のメチル,エチル,プロピル,ブチルの各エステ
ル、オレイン酸のメチル,エチル,プロピル,ブチルの
各エステル、ベヘン酸のメチル,エチル,プロピル,ブ
チル,ベヘニルの各エステル、ミリスチン酸ミリスチ
ル、ステアリン酸ステアリル、等が挙げられる。
The higher fatty acid ester represented by the above general formula of the present invention includes, for example, methyl, ethyl, propyl and butyl esters of lauric acid, methyl, ethyl, propyl and butyl esters of palmitic acid, stearic acid Methyl, ethyl, propyl, butyl esters, oleic acid methyl, ethyl, propyl, butyl esters, behenic acid methyl, ethyl, propyl, butyl, behenyl esters, myristate myristyl, stearyl stearate, And the like.

【0009】該高級脂肪酸エステルの脂肪酸の炭素数が
10未満のものは、揮発性が高く成形時に揮散して充分
な離型効果が得られない。一方脂肪酸の炭素数が22を
越えるものは、メタアクリル酸メチル系重合体との相溶
性が小さいため、樹脂表面に出易く、金型汚れ、成形品
汚れの原因となり好ましくない。
If the fatty acid of the higher fatty acid ester has less than 10 carbon atoms, it has a high volatility and volatilizes during molding, so that a sufficient releasing effect cannot be obtained. On the other hand, fatty acids having more than 22 carbon atoms are not preferred because they have a low compatibility with the methyl methacrylate-based polymer and therefore easily appear on the resin surface, causing mold stains and molded article stains.

【0010】本発明の、炭素数10〜22の高級脂肪酸
のグリセリンモノエステルとしては、例えばラウリン酸
モノグリセライド、パルミチン酸モノグリセライド、ス
テアリン酸モノグリセライド、オレイン酸モノグリセラ
イド、ベヘン酸モノグリセライドなどがあげられる。
The glycerin monoester of a higher fatty acid having 10 to 22 carbon atoms according to the present invention includes, for example, monoglyceride laurate, monoglyceride palmitate, monoglyceride stearate, monoglyceride oleate and monoglyceride behenate.

【0011】該高級脂肪酸のグリセリンモノエステルの
高級脂肪酸の炭素数が10未満のものは、揮発性が高く
成形時に揮散して充分な離型効果が得られない。一方炭
素数が22をこえるものは、メタアクリル酸メチル系重
合体との相溶性が小さいため、樹脂表面に出易く、金型
汚れ、成形品汚れの原因となり好ましくない。
The higher fatty acid glycerin monoester having a higher fatty acid having less than 10 carbon atoms has a high volatility and volatilizes during molding, so that a sufficient releasing effect cannot be obtained. On the other hand, those having more than 22 carbon atoms are not preferable because they have a low compatibility with the methyl methacrylate-based polymer and thus easily appear on the resin surface, causing mold stains and molded article stains.

【0012】本発明においては、該高級脂肪酸エステル
と、該高級脂肪酸のグリセリンモノエステルは、10/
90〜90/10、好ましくは、25/75〜75/2
5の比率で用いることにより、顕著な相乗効果が現われ
る。この比率の範囲内で、使用されるメタアクリル酸メ
チル系重合体の組成、分子量、流動性などに応じて選択
する。
In the present invention, the higher fatty acid ester and the glycerin monoester of the higher fatty acid are 10/10
90-90 / 10, preferably 25 / 75-75 / 2
By using at a ratio of 5, a remarkable synergistic effect appears. The ratio is selected within the range according to the composition, molecular weight, fluidity and the like of the methyl methacrylate polymer used.

【0013】該高級脂肪酸エステルと高級脂肪酸のグリ
セリンモノエステルの合計量は、メタアクリル酸メチル
系重合体100重量部当り0.02〜0.5重量部、好
ましくは、0.05〜0.2重量部である。これらの合
計量が0.02重量部未満の場合には、離型性能が不足
し、成形品表面層が剥離したり、割れ易くなる。一方添
加量が0.5重量部を越えた場合には、成形品の着色を
もたらし、また余剰の離型剤が金型面に付着し、金型が
汚れ、汚染された成形品となり好ましくない。
The total amount of the higher fatty acid ester and the glycerin monoester of the higher fatty acid is 0.02 to 0.5 part by weight, preferably 0.05 to 0.2 part by weight, per 100 parts by weight of the methyl methacrylate polymer. Parts by weight. If the total amount is less than 0.02 parts by weight, the release performance is insufficient, and the surface layer of the molded product is easily peeled or cracked. On the other hand, when the addition amount exceeds 0.5 parts by weight, the molded article is colored, and an excessive release agent adheres to the mold surface, and the mold is undesirably stained and contaminated. .

【0014】本発明で用いられるメタクリル酸メチル系
重合体に、該高級脂肪酸エステル、該高級脂肪酸のグリ
セリンモノエステルを含ませて、組成物とするには、周
知の方法を用いることができる。例えば、各成分を、溶
融状態で混練する方法があり、該溶融混練は、一般的に
使用されている一軸または二軸の押出機、各種のニーダ
ー等の混練装置を用いる方法のみならず、射出成形や押
出成形のごとく溶融加工操作中に直接混練する方法があ
る。
In order to make the methyl methacrylate polymer used in the present invention contain the higher fatty acid ester and the glycerin monoester of the higher fatty acid to form a composition, a well-known method can be used. For example, there is a method in which each component is kneaded in a molten state. The melt kneading is not only a method using a kneading apparatus such as a commonly used single-screw or twin-screw extruder or various kneaders, but also an injection method. There is a method of directly kneading during a melt processing operation such as molding or extrusion molding.

【0015】又、メタアクリル酸メチルを主成分とする
単量体、あるいはシロップに、該高級脂肪酸エステルと
該高級脂肪酸のグリセリンモノエステルを添加混合し、
これを塊状重合法、懸濁重合法、乳化重合法、溶液重合
法など周知の方法で重合する方法がある。
Further, the higher fatty acid ester and a glycerin monoester of the higher fatty acid are added to a monomer or syrup containing methyl methacrylate as a main component, and mixed.
There is a method of polymerizing this by a known method such as a bulk polymerization method, a suspension polymerization method, an emulsion polymerization method, and a solution polymerization method.

【0016】なお、本発明のメタクリル系樹脂組成物に
は周知のヒンダードフェノール系酸化防止剤、リン系酸
化防止剤及びイオウ系酸化防止剤等の酸化防止剤、紫外
線吸収剤やヒンダードアミン型光安定剤等の耐候剤、難
燃剤、着色剤、顔料等を添加することも出来るし、さら
に目的によってはガラス繊維等の強化繊維、無機充填剤
等も配合することも出来る。
The methacrylic resin composition of the present invention contains a known antioxidant such as a hindered phenol antioxidant, a phosphorus antioxidant and a sulfur antioxidant, an ultraviolet absorber and a hindered amine type light stabilizer. It is possible to add a weathering agent such as an agent, a flame retardant, a colorant, a pigment and the like, and further, depending on the purpose, a reinforcing fiber such as a glass fiber and an inorganic filler.

【0017】[0017]

【発明の効果】本発明のメタクリル系樹脂組成物は、従
来のメタクリル系樹脂に比べ、金型を用いて成形した際
に、優れた離型性を有し、かつメタクリル系樹脂本来の
優れた透明性、耐候性も有している。 従って、メータ
ーカバー等の自動車部品、ビデオディスク、レンズ等の
光学部品、照明部品、OA機器部品等の複雑な形状の成
形品を金型を用いて成形するのに適している。
According to the present invention, the methacrylic resin composition of the present invention has excellent releasability when molded using a mold, and has excellent methacrylic resin inherent properties, as compared with the conventional methacrylic resin. It also has transparency and weather resistance. Therefore, it is suitable for molding a molded article having a complicated shape such as an automobile part such as a meter cover, an optical part such as a video disk and a lens, a lighting part, and an OA equipment part using a mold.

【0018】[0018]

【実施例】以下実施例によって本発明をさらに説明す
る。なお、実施例において用いた評価方法は次の通り。 ・離型性:容量13オンスの射出成形機(各機製作所
製、M−140SJ型)に、25mm×76.5mm×3.
2mmのASTM試験片金型を取りつけ、成形温度260
℃、射出圧力80kg/cm2 G 、金型温度60℃の条件
下、60秒サイクルで、連続40回試験片を作成した。
この時の成形品のヒビ、ワレ等の不良品の発生した個数
の比率で表わした。 ・汚染性:前記の成形を終えた直後の金型表面(鏡面
部)の曇りの状態を目視観察して曇りが見られないもの
を○、曇りが有るものを×とした。 ・外観;成形品の汚れ、着色状況を見視で観察した。
The present invention will be further described with reference to the following examples. The evaluation method used in the examples is as follows.・ Release property: 25 mm × 76.5 mm × 3 in an injection molding machine (M-140SJ type manufactured by each machine) having a capacity of 13 oz.
A 2 mm ASTM test piece mold was attached, and the molding temperature was 260
° C., injection pressure 80 kg / cm 2 G, under the conditions of mold temperature 60 ° C., 60 seconds cycle, have created a continuous 40 times the test piece.
At this time, it was represented by the ratio of the number of defective products such as cracks and cracks in the molded product. -Stainability: The state of fogging on the mold surface (mirror surface) immediately after the completion of the above-mentioned molding was visually observed. -Appearance: The stain and coloring of the molded product were visually observed.

【0019】実施例1 懸濁重合で得られた粒状メタクリル樹脂、(スミペック
スB LO、住友化学工業(株)製)100部と、ステアリ
ン酸ブチル0.025部及びステアリン酸モノグリセラ
イド0.025部とを、ヘンシェル型ミキサーで混合
後、スクリュー径40mmのベント型押出機を用いてペレ
ット化した。該ペレットを評価した。得られた結果を表
1に示す。
Example 1 100 parts of a granular methacrylic resin (SUMIPEX BLO, manufactured by Sumitomo Chemical Co., Ltd.) obtained by suspension polymerization, 0.025 parts of butyl stearate and 0.025 parts of monoglyceride stearate were used. Was mixed with a Henschel mixer and then pelletized using a vent type extruder having a screw diameter of 40 mm. The pellet was evaluated. Table 1 shows the obtained results.

【0020】実施例2〜5、比較例1〜4 ステアリン酸ブチル及びステアリン酸モノグリセライド
の添加量を表1に示すように変更した以外は、実施例1
と同様に行った。得られた結果を表1に示す。
Examples 2 to 5 and Comparative Examples 1 to 4 Example 1 was repeated except that the amounts of butyl stearate and monoglyceride stearate were changed as shown in Table 1.
The same was done. Table 1 shows the obtained results.

【0021】実施例6 ステアリン酸ブチルに代えて、ステアリン酸ステアリル
とした以外は、実施例2と同様に行った。得られた結果
を表1に示す。
Example 6 The procedure of Example 2 was repeated, except that stearyl stearate was used instead of butyl stearate. Table 1 shows the obtained results.

【0022】実施例7 ステアリン酸モノグリセライドに代えて、パルミチン酸
モノグリセライドとした以外は、実施例2と同様に行っ
た。得られた結果を表1に示す。
Example 7 The procedure of Example 2 was repeated except that monoglyceride palmitate was used instead of monoglyceride stearate. Table 1 shows the obtained results.

【0023】[0023]

【表1】 [Table 1]

フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C08L 33/12 C08K 5/10 Continuation of front page (58) Field surveyed (Int.Cl. 7 , DB name) C08L 33/12 C08K 5/10

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】メタクリル酸メチル系重合体100重量部
に、下記一般式、 【化1】R1COOR2 (式中、R1は炭素数10〜22の脂肪族炭化水素基、
2は炭素数1〜22のアルキル基を示す)で表される
高級脂肪酸エステルと、炭素数10〜22の高級脂肪酸
のグリセリンモノエステルを重量比10/90〜90/
10で、0.02〜0.5重量部、及び必要に応じて紫
外線吸収剤、耐候剤、難燃剤、着色剤、顔料、強化繊維
または無機充填剤を含有し、その他のものを含有しない
メタクリル系樹脂組成物。
1. A method according to claim 1, wherein 100 parts by weight of a methyl methacrylate polymer is represented by the following general formula: R 1 COOR 2 (wherein R 1 is an aliphatic hydrocarbon group having 10 to 22 carbon atoms,
R 2 represents an alkyl group having 1 to 22 carbon atoms) and a glycerin monoester of a higher fatty acid having 10 to 22 carbon atoms in a weight ratio of 10/90 to 90 /
10, 0.02 to 0.5 parts by weight , and if necessary purple
External absorbent, weathering agent, flame retardant, colorant, pigment, reinforced fiber
Or a methacrylic resin composition containing an inorganic filler and no other .
JP06469792A 1992-03-23 1992-03-23 Methacrylic resin composition Expired - Lifetime JP3163723B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06469792A JP3163723B2 (en) 1992-03-23 1992-03-23 Methacrylic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06469792A JP3163723B2 (en) 1992-03-23 1992-03-23 Methacrylic resin composition

Publications (2)

Publication Number Publication Date
JPH05262950A JPH05262950A (en) 1993-10-12
JP3163723B2 true JP3163723B2 (en) 2001-05-08

Family

ID=13265605

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06469792A Expired - Lifetime JP3163723B2 (en) 1992-03-23 1992-03-23 Methacrylic resin composition

Country Status (1)

Country Link
JP (1) JP3163723B2 (en)

Also Published As

Publication number Publication date
JPH05262950A (en) 1993-10-12

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