JPH0641385A - Methacrylic resin composition - Google Patents

Methacrylic resin composition

Info

Publication number
JPH0641385A
JPH0641385A JP19686692A JP19686692A JPH0641385A JP H0641385 A JPH0641385 A JP H0641385A JP 19686692 A JP19686692 A JP 19686692A JP 19686692 A JP19686692 A JP 19686692A JP H0641385 A JPH0641385 A JP H0641385A
Authority
JP
Japan
Prior art keywords
methacrylic resin
methyl methacrylate
resin composition
alcohol
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
JP19686692A
Other languages
Japanese (ja)
Inventor
Takeshi Hashimoto
剛 橋本
Takashi Sakamoto
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 JP19686692A priority Critical patent/JPH0641385A/en
Publication of JPH0641385A publication Critical patent/JPH0641385A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide the methacrylic resin composition, having excellent mold release properties in molding processing with a metallic mold and excellent in transparency and weather resistance by adding specific methylolpropanes and a specified alcohol together to a methyl methacrylate-based polymer. CONSTITUTION:The composition is obtained by blending (A) a methyl methacrylate-based polymer with (B) trimethylolpropanes selected from formulas I and II [each of X<1>, to X<8> is H, formula III (R is 10-22C hydrocarbon), etc.] and (C) a 10-22C saturated aliphatic alcohol so as to provide (10/90) to (90/10) weight ratio of the components (B)/(C) and 0.02-0.5 pt.wt. total amount of the components (B) and (C) based on 100 pts.wt. component (A). For example, monotrimethylolpropane is cited as the component (B) and, e.g. lauryl alcohol can be used as the component (C).

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ア
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アクリル系樹脂
組成物に関する物である。
FIELD OF THE INVENTION 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 mold releasability at the time of molding using a mold.

【0002】[0002]

【従来の技術】メタアクリル系樹脂は、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 Methacrylic resins are used for automobile parts such as meter covers, optical parts such as optical discs and lenses, and electric lamp covers, etc. by taking advantage of their excellent transparency, weather resistance and good mechanical properties. It is used for lighting parts, etc. 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 becomes extremely high. Mold release failure occurs, resulting in a decrease in productivity.

【0003】そこでメタア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61-737
54号公報には、メタアクリル系樹脂に、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。
Therefore, it has been proposed to add various releasing agents to the methacrylic resin. For example, Japanese Patent Laid-Open No. 61-737
Japanese Unexamined Patent Publication No. 54-54 proposes a resin composition obtained by adding 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 to a methacrylic resin.

【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 using these resin compositions, some degree of mold release performance is recognized, but it is still insufficient. In addition, the release agent and other additives added to the resin migrate to the surface of the resin to stain the surface of the mold or the surface of the molded product and to color the molded product, thereby significantly reducing 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
るメタア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 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〔化3〕又は〔化
4〕で表されるトリメチロールプロパン類から選ばれた
少なくとも1種と炭素数10〜22の飽和脂肪族アルコ
ールを重量比10/90〜90/10で、0.02〜
0.5重量部を含有してなるメタアクリル系樹脂組成物
に関するものである。
The present invention comprises 100 parts by weight of a methyl methacrylate polymer and at least one selected from trimethylolpropanes represented by the following [Chemical formula 3] or [Chemical formula 4]. A saturated aliphatic alcohol having 10 to 22 carbon atoms in a weight ratio of 10/90 to 90/10 and 0.02 to
The present invention relates to a methacrylic resin composition containing 0.5 part by weight.

【0007】[0007]

【化3】 [Chemical 3]

【0008】式中X1 ,X2 ,及びX3 は、下記〔外
2〕で示されるものの1つである。
In the formula, X 1 , X 2 and X 3 are ones shown in the following [External 2].

【0009】[0009]

【外2】 [Outside 2]

【0010】[0010]

【化4】 [Chemical 4]

【0011】式中X4 ,X5 ,X6 ,X7 及びX8 は、
上記X1 ,X2 ,及びX3 に同じ、nは0〜3である。
Where X 4 , X 5 , X 6 , X 7 and X 8 are
Same as the above X 1 , X 2 , and X 3 , and n is 0 to 3.

【0012】本発明でいうメタアクリル酸メチル系重合
体とは、メタアクリル酸メチル単独重合体、またはメタ
アクリル酸メチルと20重量%以下のアクリル酸エステ
ルもしくはメタアクリル酸エステル、アクリル酸、メタ
アクリル酸、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、メタアクリル酸エステルとしてはメタアクリル
酸エチル、メタアクリル酸ブチル、メタアクリル酸シク
ロヘキシルなどである。
The term "methyl methacrylate polymer" as used in the present invention means methyl methacrylate homopolymer, or methyl methacrylate and 20% by weight or less of acrylic acid ester or methacrylic acid ester, acrylic acid, methacrylic acid. It refers to a copolymer with acid, styrene, acrylonitrile, diene rubber, glutaric anhydride, glutarimide, or the like. The acrylic ester is methyl acrylate, ethyl acrylate, butyl acrylate, etc., and the methacrylic ester is ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, etc.

【0013】本発明の上記〔化3〕又は〔化4〕で示さ
れるトリメチロールプロパン類としては、モノトリメチ
ロールプロパン,ジトリメチロールプロパン,トリトリ
メチロールプロパン,テトラトリメチロールプロパン,
及びペンタトリメチロールプロパン、及びこれらのトリ
メチロールプロパンとラウリン酸,ミリスチン酸,ステ
アリン酸,ベヘン酸,オレイン酸,リノール酸,リノレ
ン酸等の如き炭素数10〜22の炭化水素基Rを有する
カルボン酸との各エステル化合物、更にはこれらのトリ
メチロールプロパンのエチレンオキシド及び/又はプロ
ピレンオキシドの1〜5個の付加物等が挙げられる。
The trimethylolpropanes represented by the above [Chemical formula 3] or [Chemical formula 4] of the present invention include monotrimethylolpropane, ditrimethylolpropane, tritrimethylolpropane, tetratrimethylolpropane,
And pentatrimethylolpropane, and trimethylolpropane and carboxylic acids having a hydrocarbon group R having 10 to 22 carbon atoms such as lauric acid, myristic acid, stearic acid, behenic acid, oleic acid, linoleic acid and linolenic acid And ester compounds thereof, and addition products of 1 to 5 ethylene oxide and / or propylene oxide adducts of trimethylolpropane.

【0014】該トリメチロールプロパンのカルボン酸と
の各エステル化合物の炭化水素基R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を超えるものは、メ
タ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。又、前記〔化3〕又は〔化4〕のf、gが
5を超えるもの、及び〔化4〕のnが3を超えるもの
は、メタ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 hydrocarbon group R of each ester compound with carboxylic acid of trimethylolpropane has a carbon number of less than 10, it has a high volatility and volatilizes during molding, and a sufficient releasing effect cannot be obtained. On the other hand, those having more than 22 carbon atoms are not preferable because they have low compatibility with the methyl methacrylate-based polymer, so that they easily appear on the resin surface and cause mold stains and molded product stains. Further, those in which f and g in [Chemical Formula 3] or [Chemical Formula 4] exceed 5 and those in which n in [Chemical Formula 4] exceeds 3 have low compatibility with a methyl methacrylate polymer, It is not preferable because it easily appears on the resin surface and causes stains on the mold and molded articles.

【0015】本発明の、炭素数10〜22の飽和脂肪族
アルコールとしては、例えばラウリルアルコール、ミリ
スチルアルコール、セチルアルコール、ステアリルアル
コール、イソステアリルアルコール、ベヘニルアルコー
ル等が挙げられる。
Examples of the saturated aliphatic alcohol having 10 to 22 carbon atoms in the present invention include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, isostearyl alcohol and behenyl alcohol.

【0016】該飽和脂肪族アルコールの炭素数が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。
When the saturated aliphatic alcohol has less than 10 carbon atoms, it has a high volatility and is volatilized during molding, and a sufficient releasing effect cannot be obtained. On the other hand, if the carbon number exceeds 22,
Since it has a low compatibility with the methyl methacrylate polymer, it tends to appear on the resin surface, causing mold stains and molded product stains.

【0017】本発明においては、該トリメチロールプロ
パン類と、該飽和脂肪族アルコールは、10/90〜9
0/10、好ましくは、25/75〜75/25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 trimethylolpropanes and the saturated aliphatic alcohol are 10/90 to 9
When used in a ratio of 0/10, preferably 25/75 to 75/25, a remarkable synergistic effect appears. Within the range of this ratio, it is selected according to the composition, molecular weight, fluidity and the like of the methyl methacrylate polymer used.

【0018】該トリメチロールプロパン類と該飽和脂肪
族アルコールの合計量は、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 trimethylolpropanes and the saturated aliphatic alcohol is 0.02 to 0.5 part by weight, preferably 0.05 to 0.2, based on 100 parts by weight of the methyl methacrylate polymer. Parts by weight. If the total amount of these is less than 0.02 parts by weight, the release performance is insufficient, and the surface layer of the molded product is likely to peel off or crack. On the other hand, when the addition amount exceeds 0.5 parts by weight, the molded product is colored, and the excess mold release agent adheres to the mold surface, and the mold becomes dirty.
It is not preferable because it becomes a contaminated molded product.

【0019】本発明で用いられるメタアクリル酸メチル
系重合体に、該トリメチロールプロパン類、該飽和脂肪
族アルコールを含ませて、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。
A well-known method can be used to prepare the composition by incorporating the trimethylolpropanes and the saturated aliphatic alcohol into the methyl methacrylate polymer used in the present invention. For example, there is a method of kneading each component in a molten state, and the melt kneading is not limited to a method using a commonly used kneading device such as a single-screw or twin-screw extruder, various kneaders, and injection. There is a method of directly kneading during a melt processing operation such as molding and extrusion molding.

【0020】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、該トリメチロールプロパ
ン類と該飽和脂肪族アルコールを添加混合し、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 trimethylolpropanes and the saturated aliphatic alcohol are added to and mixed with a monomer or syrup containing methyl methacrylate as a main component, and the mixture is subjected to a bulk polymerization method, a suspension polymerization method or an emulsification method. There are known methods such as a polymerization method and a solution polymerization method.

【0021】なお、本発明のメタア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 includes well-known antioxidants such as hindered phenolic antioxidants, phosphorus antioxidants and sulfur antioxidants, ultraviolet absorbers and hindered amine type photopolymers. Weathering agents such as stabilizers,
Flame retardants, colorants, pigments and the like can be added, and further, reinforcing fibers such as glass fibers and inorganic fillers can be added depending on the purpose.

【0022】[0022]

【発明の効果】本発明のメタアクリル系樹脂組成物は、
従来のメタア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、かつメタアクリル系樹脂
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。
The methacrylic resin composition of the present invention is
Compared with the conventional methacrylic resin, it has excellent releasability when molded by using a mold, and also has excellent transparency and weather resistance inherent to the methacrylic resin. Therefore,
It is suitable for molding molded articles having complicated shapes such as automobile parts such as meter covers, optical parts such as video disks and lenses, lighting parts, OA equipment parts, etc. using a mold.

【0023】[0023]

【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 methods used in the examples are as follows. -Releasability: Injection molding machine with capacity of 13 ounces (M-140SJ type, manufactured by each machine) with 25 mm x 76.5 mm x 3.
Attach a 2mm ASTM test piece mold, molding temperature 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.
It was expressed by the ratio of the number of defective products such as cracks and cracks in the molded product at this time. Stainability: Immediately after completion of the above-mentioned molding, the state of cloudiness on the surface of the mold (mirror surface part) was visually observed, and when no cloudiness was observed, it was rated as O, and when there was cloudiness, was rated as X. -Appearance: The stains and coloring of the molded product were visually observed.

【0024】実施例1 懸濁重合で得られた粒状メタアクリル樹脂、(スミペッ
クスB LO、住友化学工業(株)製)100部と、ジトリ
メチロールプロパン・プロピレンオキシド3付加物0.
025部及びステアリルアルコール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 obtained by suspension polymerization (Sumipex B LO, manufactured by Sumitomo Chemical Co., Ltd.) and ditrimethylolpropane / propylene oxide 3 adduct.
025 parts and stearyl alcohol 0.025 parts,
After mixing with a Henschel type mixer, pelletization was performed using a vent type extruder having a screw diameter of 40 mm. The pellets were evaluated. The results obtained are shown in Table 1.

【0025】実施例2〜5、比較例1〜4 ジトリメチロールプロパン・プロピレンオキシド3付加
物及びステアリルアルコールの添加量を表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 The procedure of Example 1 was repeated, except that the addition amounts of ditrimethylolpropane / propylene oxide 3 adduct and stearyl alcohol were changed as shown in Table 1. The results obtained are shown in Table 1.

【0026】実施例6 ジトリメチロールプロパン・プロピレンオキシド3付加
物に代えて、ジトリメチロールプロパンとした以外は、
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 Except that ditrimethylolpropane-propylene oxide 3 adduct was replaced by ditrimethylolpropane,
The same procedure as in Example 2 was performed. The results obtained are shown in Table 1.

【0027】実施例7 ステアリルアルコールに代えて、セチルアルコールとし
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 7 Example 2 was repeated except that cetyl alcohol was used instead of stearyl alcohol. The results obtained are shown in Table 1.

【0028】[0028]

【表1】 注 はジトリメチロールプロパンプロピレンオキシド
3付加物 はジトリメチロールプロパン を示す。
[Table 1] Note: Ditrimethylolpropane propylene oxide 3 adduct is ditrimethylolpropane.

Claims (1)

【特許請求の範囲】[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〔化1〕又は〔化2〕で表されるトリメチロー
ルプロパン類から選ばれた少なくとも1種と炭素数10
〜22の飽和脂肪族アルコールを重量比10/90〜9
0/10で、0.02〜0.5重量部を含有してなるメ
タアクリル系樹脂組成物。 【化1】 式中X1 ,X2 ,及びX3 は、下記〔外1〕で示される
ものの1つである。 【外1】 【化2】 式中X4 ,X5 ,X6 ,X7 及びX8 は、上記X1 ,X
2 ,及びX3 に同じ、 nは0〜3である。
1. To 100 parts by weight of a methyl methacrylate polymer, at least one selected from trimethylolpropanes represented by the following [Chemical formula 1] or [Chemical formula 2] and 10 carbon atoms.
~ 22 saturated aliphatic alcohol in a weight ratio of 10 / 90-9
A methacrylic resin composition, which is 0/10 and contains 0.02 to 0.5 part by weight. [Chemical 1] In the formula, X 1 , X 2 , and X 3 are ones shown in [External 1] below. [Outer 1] [Chemical 2] In the formula, X 4 , X 5 , X 6 , X 7 and X 8 are the above-mentioned X 1 , X
The same as 2 and X 3 , n is 0 to 3.
JP19686692A 1992-07-23 1992-07-23 Methacrylic resin composition Pending JPH0641385A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19686692A JPH0641385A (en) 1992-07-23 1992-07-23 Methacrylic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19686692A JPH0641385A (en) 1992-07-23 1992-07-23 Methacrylic resin composition

Publications (1)

Publication Number Publication Date
JPH0641385A true JPH0641385A (en) 1994-02-15

Family

ID=16364955

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19686692A Pending JPH0641385A (en) 1992-07-23 1992-07-23 Methacrylic resin composition

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009125768A1 (en) 2008-04-08 2009-10-15 住友化学株式会社 Methacrylic resin composition for hot plate melt-bonding, use of the same for hot plate melt-bonding, and melt-bonding method
WO2009125764A1 (en) 2008-04-08 2009-10-15 住友化学株式会社 Methacrylic resin composition for hot plate melt-bonding, use of the same for hot plate melt-bonding, and melt-bonding method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009125768A1 (en) 2008-04-08 2009-10-15 住友化学株式会社 Methacrylic resin composition for hot plate melt-bonding, use of the same for hot plate melt-bonding, and melt-bonding method
WO2009125764A1 (en) 2008-04-08 2009-10-15 住友化学株式会社 Methacrylic resin composition for hot plate melt-bonding, use of the same for hot plate melt-bonding, and melt-bonding method
KR20160025036A (en) 2008-04-08 2016-03-07 스미또모 가가꾸 가부시끼가이샤 Methacrylic resin composition for hot plate melt-bonding, use of the same for hot plate melt-bonding, and melt-bonding method

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