JPS58104939A - Methacrylic resin composition - Google Patents

Methacrylic resin composition

Info

Publication number
JPS58104939A
JPS58104939A JP56204731A JP20473181A JPS58104939A JP S58104939 A JPS58104939 A JP S58104939A JP 56204731 A JP56204731 A JP 56204731A JP 20473181 A JP20473181 A JP 20473181A JP S58104939 A JPS58104939 A JP S58104939A
Authority
JP
Japan
Prior art keywords
weight
impact
methacrylic resin
methyl methacrylate
copolymer
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
JP56204731A
Other languages
Japanese (ja)
Inventor
Kazumasa Kamata
釜田 和正
Yasunobu Shimomura
下村 泰宣
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.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon 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 Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP56204731A priority Critical patent/JPS58104939A/en
Publication of JPS58104939A publication Critical patent/JPS58104939A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Optical Record Carriers And Manufacture Thereof (AREA)

Abstract

PURPOSE:To prepare a composition having excellent optical properties and impact resistance as well as remarkably reduced moisture absorption, by compounding a copolymer composed of methyl methacrylate and cyclohexyl methacrylate with an impact-resistant acrylic resin. CONSTITUTION:The objective composition is prepared by compounding (A) 70- 98pts.wt., preferably 80-95pts.wt. of a copolymer composed of (a) 50-85wt% (in terms of monomer) methyl methacrylate, (b) 15-50wt% cyclohexyl methacrylate and (c) 0-10% other vinyl monomer copolymerizable therewith with (B) 2-30pts.wt., preferably 5-20pts.wt. of an impact-resistant acrylic resin containing a crosslinked acrylic acid ester polymer as the rubber component. The heat decomposition resistance of the composition can be improved by using a vinyl compound, preferably a compound containing 0.2-10% alkyl acrylate having 1-8C alkyl, as a component of the component (A).

Description

【発明の詳細な説明】 本発明はメタクリル樹脂組成物に関する□メタクリル酸
メチルを主成分とするメタクリル樹脂は透明性ならびに
耐候性に極めて優れた特性を有しているはかりでなく、
機械的性iit。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a methacrylic resin composition □Methacrylic resin whose main component is methyl methacrylate has extremely excellent properties in terms of transparency and weather resistance.
mechanical iit.

熱的性質、成形加工性などにもバランスのとれたマぐれ
た性質を有しており、これらの特徴を生かしてシート材
料あるいは成形材料として看板、照明機器部品1電気機
器部品、自動車部品、維貨なと多方面に使用されている
It has well-balanced properties such as thermal properties and moldability, and by taking advantage of these characteristics, it can be used as a sheet material or molding material for signboards, lighting equipment parts, electrical equipment parts, automobile parts, and maintenance materials. It is used in many ways as currency.

また最近−メタクリル樹脂は透明性をはじめ・そのすぐ
れた性質を生かし、ビデオディスク・オーディオディス
ク、コンピューター用情報、ファイルディスク等の情報
記録体用材料として使用されはじめた〇 特に情報記録体用の基板としては装置で取扱いが容易な
点から塩化ビニルミt脂・ポリスチレン、メタクリル樹
脂等のシート、フィルムの使用が提案されているが、メ
タクリル他側は光線透過率に優れ、塩化ビニル樹脂に比
べて傷がっきにくい・複屈折率が低い、表面精度が良好
で仕上りが美しい等の特徴を有するため、特にレーザー
光により光学的に再生する方式の情報記録体にはメタク
リル樹脂が適している。
Recently, methacrylic resin has begun to be used as a material for information recording media such as video discs, audio discs, computer information, file discs, etc., taking advantage of its transparency and other excellent properties.In particular, methacrylic resin has been used as a material for information recording media, such as substrates for information recording media. The use of sheets and films made of vinyl chloride resin, polystyrene, methacrylic resin, etc. has been proposed because they are easy to handle with equipment, but methacrylic on the other side has excellent light transmittance and is less susceptible to scratches than vinyl chloride resin. Methacrylic resin is particularly suitable for information recording media that are optically reproduced using laser light because it has characteristics such as being resistant to flaking, having a low birefringence, and having good surface precision and a beautiful finish.

しかしながらメタクリル樹脂はポリオレフィン糸樹脂、
ポリスチレン系樹脂に比べ比較的吸湿性が大きく、吸湿
による寸法変化、成形品のそり、あるいは吸湿と乾燥の
長期くり返しサイクルによるクラック発生などを生ずる
ことがあり、通常のメタクリル樹脂はその使用が制約さ
れている分野もある。特にビデオディスク、オーディオ
ディスク、大容量画像ファイル、大容量コンピューター
用ディスクメモリー等の情報□ 記録体用材料としては成形品にそりを生じないこと等、
高度の寸法安定性が要求されており、吸湿性の低減され
たメタクリル系脂の提供が要望されている◎ このメタクリル樹脂の吸湿性の問題はある程度そのポリ
マーの化学構造に起因する本質的な性質であり、今まで
にその改質方法についての提案もほとんどなく、もちろ
ん商品化も行なわれていないのが現状である。
However, methacrylic resin is polyolefin thread resin,
It has relatively high hygroscopicity compared to polystyrene resins, and may cause dimensional changes due to moisture absorption, warpage of molded products, or cracks due to long repeated cycles of moisture absorption and drying, which limits the use of ordinary methacrylic resins. There are some fields where In particular, information such as video discs, audio discs, large-capacity image files, large-capacity computer disk memories, etc. □ As recording material, molded products should not warp, etc.
A high degree of dimensional stability is required, and there is a demand for the provision of methacrylic resins with reduced hygroscopicity.◎ The hygroscopicity problem of methacrylic resins is to some extent an inherent property caused by the chemical structure of the polymer. So far, there have been few proposals regarding the reforming method, and of course, the current situation is that it has not been commercialized.

本発明者らはこのような現状に鑑み、メタクリル樹脂の
吸湿性を改善し、かつ機械的強度がすぐれ、光学的特性
のすぐれたメタクリル樹脂を開発すべく鋭意研究を進め
た結果・メタクリル酸メチルにメタクリル酸シクロヘキ
シルおよび他の共重合性ビニル単量体を特定社共本合さ
せることにより、従来より知られていた光学的性質とは
全く別なメタクリル酸メチル重合体の吸湿性が大幅に低
減されるという全く新しい作用効果を見出し、さらにメ
タクリル酸メチル、メタクリル酸シクロヘキシルおよび
他の共重合性ビニルからなる共重合体(1)と耐衝撃性
アクリ1:: ル樹脂(II)との特定成分範囲内のブレンド物におい
てツー直材料および、形材料おり、”i(6明性、1:
1 耐候性、機械的性質、熱的性質および成形DII上性な
どメタクリル樹脂本来の優れた特性を有しているととも
に、吸湿性が通常のメタクリル樹脂に比べて大幅に低減
され、情報記録体用材料に最も適した組成物が得られる
ことを見出し1本発明に到達した□ すなわち本発明は単量体成分に換算してメタクリル酸メ
チル囚5oNzj重量襲、メタクリル酸シクロヘキシル
(Jl)/!〜j0重量襲−および囚および慟)と共重
合可能な他のビニル単量体(C)0〜IO重量外とから
なる共富合体中70〜wig量部と架橋アクリル酸エス
テル系重合体゛をゴム成分とした耐衝撃性アクリル1樹
脂(II)2〜30重量部(合計100重量部)からな
るメタクリル樹脂組成物である・ 本発明のメタクリル系樹脂の共重合成分として用いるメ
タクリル酸シクロヘキシルの単独重合体は他のメタクリ
レート重合体に比べ屈折率が高く、かつ光の分散特性も
優れているのでプラスチックレンズ素材−とじて優れた
基本性能を有していることは以前より知られていたが、
メタクリル酸シクロヘキシルの単独重合体は非常にも−
ろく、一般的な成形加工も困難な状況にあり、実用に供
するためには極めて大きな問題があった0 本発明は光学的特性に優れ、かつ吸湿性の改善されるメ
タクリル瘤メチルーメタクリル醒シクロヘキシル糸共重
合体とアクリル糸耐衝撃性樹脂とのブレンド物が光学的
特性、低吸湿性に優れ・かつ耐衝撃性の改善されたメタ
クリル系樹脂を与えφことを見出したものである0本発
明の共重合体(l)において、メタタ11 )し酸メチ
ル(4)の隼用割合30〜gs1に@%G) ?1られ
る共重合体中にメタクリル樹脂本来の光学的性質、耐候
、性ご機械的性質、熱的性質あるいは成形加工性を付与
するために必要な組成範囲であり、より好ましくはSS
〜tS重量%である。
In view of the current situation, the present inventors conducted intensive research to improve the hygroscopicity of methacrylic resin, and to develop a methacrylic resin with excellent mechanical strength and optical properties.Methyl methacrylate By co-merging cyclohexyl methacrylate and other copolymerizable vinyl monomers with methyl methacrylate, the hygroscopicity of methyl methacrylate polymer, which has completely different optical properties than previously known, has been significantly reduced. In addition, we discovered a completely new function and effect in which methyl methacrylate, cyclohexyl methacrylate, and other copolymerizable vinyls are used as specific components of copolymer (1) and impact-resistant acrylic resin (II). In the blends within the range of two direct materials and shaped materials, "i (6 brightness, 1:
1 It has the excellent properties inherent to methacrylic resin, such as weather resistance, mechanical properties, thermal properties, and molding DII properties, and its hygroscopicity is significantly lower than that of ordinary methacrylic resin, making it suitable for information recording media. The present invention was achieved by discovering that a composition most suitable for the material can be obtained□ That is, the present invention is based on methyl methacrylate (5oNzj weight), cyclohexyl methacrylate (Jl)/! in terms of monomer components. 70 to 10 parts by weight in a co-enriched polymer consisting of other vinyl monomers (C) copolymerizable with 0 to 10% by weight and 0 to 10% by weight and a crosslinked acrylic acid ester polymer. It is a methacrylic resin composition consisting of 2 to 30 parts by weight (total 100 parts by weight) of impact-resistant acrylic 1 resin (II) containing as a rubber component cyclohexyl methacrylate used as a copolymerization component of the methacrylic resin of the present invention. It has been known for some time that homopolymers have a higher refractive index than other methacrylate polymers and excellent light dispersion properties, so they have excellent basic performance as plastic lens materials. ,
Homopolymers of cyclohexyl methacrylate are very
However, the general molding process is also difficult, and there are extremely serious problems in putting it into practical use. The present invention is based on the discovery that a blend of a yarn copolymer and an acrylic yarn impact-resistant resin provides a methacrylic resin with excellent optical properties, low moisture absorption, and improved impact resistance. In the copolymer (l), the ratio of methyl metata-11) phosphate (4) to 30~gs1 @%G)? This is the composition range necessary for imparting the optical properties, weather resistance, mechanical properties, thermal properties, or moldability inherent to methacrylic resin to the copolymer prepared in 1, and more preferably SS.
~tS wt%.

メタクリル酸メチル成分の使用割合がSO東量%未満で
は、上記の特性が損われ、逆にZS本量%をこえると吸
湿性の改善効果が少なくなるからである◎ また1、メタクリル酸−シクロヘキシル(B)の使用割
合/!r−jO重量%は、得られる共重合体σ)吸湿性
を改善するために必要な成分量であり、より好ましくは
一〇−13重1%である073重置重置溝では吸湿性改
質の効果が十分でなくSO型重量外こえると機械的強度
が大きく低下するからである□また共重合体に必要に応
じて用いることのできる囚および悌)と共重合可能な他
のビニル単量体(Qの異体例としては、たとえばメチル
アクリレート、エチルアクリレート、ブチルアクリレー
ト、スチレン、アクリロニトリル等を挙げることができ
使用割合としては10車置%以下がよい。
If the usage ratio of methyl methacrylate component is less than SO content%, the above properties will be impaired, and conversely, if it exceeds ZS content%, the effect of improving hygroscopicity will be reduced. 1. Cyclohexyl methacrylate Usage rate of (B)/! r-jO weight% is the amount of component necessary to improve the hygroscopicity of the resulting copolymer σ), and more preferably 10-13% by weight in the 073 overlapping groove, the hygroscopicity improvement is This is because if the quality effect is not sufficient and the weight exceeds the SO type weight, the mechanical strength will be greatly reduced.In addition, other vinyl monomers that can be copolymerized with Examples of different isomers of the polymer (Q) include methyl acrylate, ethyl acrylate, butyl acrylate, styrene, acrylonitrile, etc., and the proportion used is preferably 10% or less.

特に本発明の共重合体を成形材料として実用に供Tる場
合には・比較的高温域での成形を考慮し、共重合体の耐
熱分解性を向上させるため、02〜10gg%のビニル
化合物(C)を用いることが好ましい□O))の使用割
合がaコ重量外未満の場合には耐熱分解性が充分でなく
、またIO、:′:。
In particular, when the copolymer of the present invention is put to practical use as a molding material, in order to improve the thermal decomposition resistance of the copolymer in consideration of molding in a relatively high temperature range, 0.2 to 10 g% of a vinyl compound is added. It is preferable to use (C). If the proportion of □O)) used is less than the weight of a, the heat decomposition resistance will be insufficient, and IO, :':.

重量%を超える場合には透明性が低下したり、吸湿性が
低下したり、耐熱変形温度が低下したりする間層がある
◎ビニル化合物(C)としては炭素数/−gのアルキル
基を有するアルキルアクリレート、例えばアクリル酸エ
チル、アクリル酸ブチル、アクリル#に一一エチルヘキ
シル等を用いるのが耐熱分解性、吸湿性、耐熱変形性の
点から好ましい。
If it exceeds % by weight, there will be an interlayer that will reduce transparency, hygroscopicity, and heat deformation resistance.◎The vinyl compound (C) contains an alkyl group with carbon number/-g. It is preferable to use an alkyl acrylate such as ethyl acrylate, butyl acrylate, 1-ethylhexyl for acrylic acid, etc. from the viewpoint of heat decomposition resistance, hygroscopicity, and heat deformation resistance.

本発明の共重合体中の使用割合の70−9g重量部はg
&湿性を改質するためのものであり、より好ましくはg
O〜95本fitsである。共重合体(IJの使用割合
が70重量部より少ないと1吸湿性の改質効果が小さく
、9g重處都より多いと機械的強度の向上が望めないか
らである。
The proportion of 70-9g weight used in the copolymer of the present invention is g
& for modifying wettability, more preferably g
O~95 fits. This is because if the proportion of copolymer (IJ) used is less than 70 parts by weight, the effect of improving hygroscopicity is small, and if it is more than 9 g weight, no improvement in mechanical strength can be expected.

本発明の架橋アクリル酸エステル系本合体をゴム成分と
した耐衝撃性樹脂(n)の使用割合の1〜30重量部は
機械的強度を向上させるためのものであり、−重置都よ
り少ないと機械的強度の向上が望めず3q重盪部より多
いと吸湿性の改質効果が小さくJ光学的特性が劣る□よ
り好::、。
The proportion of 1 to 30 parts by weight of the impact-resistant resin (n) containing the crosslinked acrylic acid ester main composite of the present invention as a rubber component is for improving mechanical strength, and is less than - It is better than □ that no improvement in mechanical strength can be expected, and if it is more than 3q parts, the effect of modifying hygroscopicity is small and J optical properties are poor.

ましくはj−一〇本量部がよい。架橋アクリル酸エステ
ル系本合体をゴム成分とした耐衝撃性樹脂の具体的な製
造方法としては、例えばまずエチルアクリレート、n−
ブチルアクリレート、−一エチルヘキシルアクリレート
などのアクリル酸エステル70〜/DO重重外、これと
共重合可能なメタクリル酸メチル、アクリロニトリル、
スチレンなどの単量体θ〜30*量襲および7分子中に
少なくともコ個の戻素−炭素のコ本結合を含有する架橋
性単量体a/〜SJ!量外よりなる単量体混合物を乳化
重合して粒子径1203〜ajμの架11ゴムラテック
スを製造する。次いでこのラテックスの存在下にアクリ
ロニトリル、スチレンおよびメタクリル酸メチルなどの
単量体をグラフト重合して架橋アクリル酸エステル系重
合体をゴム成分とした耐衝撃性m脂をラテツタス状で得
1これを凝固\乾燥して、本発明に使用する成分の樹脂
を得ることができる□この種の樹脂として市販されてい
るものには三菱レイヨン(株)製の[ダイヤラック−A
J及び「アクリベットIR」、ロームアンドハース社朧
の「プレキシグラスDR」、日立化成工業(株)製の「
パイタラクズ」などがある。
Preferably, the amount is j-10 parts. As a specific method for producing an impact-resistant resin containing a crosslinked acrylic acid ester-based polymer as a rubber component, for example, first, ethyl acrylate, n-
Acrylic acid esters such as butyl acrylate, -monoethylhexyl acrylate, etc. 70~/DO polyester, methyl methacrylate copolymerizable with this, acrylonitrile,
Monomers such as styrene θ~30* weight ratio and crosslinkable monomers a/~SJ containing at least 0 return element-carbon bonds in 7 molecules! A monomer mixture consisting of a different amount is emulsion polymerized to produce a frame 11 rubber latex having a particle size of 1203 to ajμ. Next, in the presence of this latex, monomers such as acrylonitrile, styrene, and methyl methacrylate are graft-polymerized to obtain a latte-like impact-resistant resin containing a crosslinked acrylic acid ester polymer as a rubber component.1 This is solidified. \The resin of the component used in the present invention can be obtained by drying. □ Commercially available resins of this type include [Dialac-A] manufactured by Mitsubishi Rayon Co., Ltd.
J and "Acrivet IR", "Plexiglas DR" by Rohm and Haas Oboro, "
"Pytarakuzu" etc.

以上が本発明を@成している必須成分と千の配合比であ
るが本発明の組成物を具体的に得るには前記した樹脂を
本発明の範囲内に秤慮した後ヘンシェルミキサーあるい
は■型プレンダーで混合した後、押出機を用いてペレッ
ト化してもよいし1架橋アクリル酸工ステル糸本合体を
ゴム成分とした耐衝撃性樹脂な単量体混合物に溶解後、
塊状東金あるいは懸濁重合することによって得ることも
できる0 本発明の組成物には必要に応じて染顔料、紫外線吸収剤
及び酸化安定剤等を加えることができる・ 以下実施例によって本発明の内容を更に具体的に説明す
る0 実施例7〜コ、 比較例1−コ コンデンサー、攪拌機、温度計をそなえたjノのセパラ
ブルフラスコに、分散剤としてメタクリル酸メチルとぎ
タシウムスル7オブロビルメタクリレートとの共重合体
Q!溶解した水30009を入れ、別に!Ill整した
メタクリル酸メチル!フz9sメタタリル酸シクロヘキ
シルダ30g、アクリル酸ブチル7j9の単量体混合物
にn−オクチルメルカプタン3gおよびアゾビスイソブ
千四ニトリル119を溶解した該混合物をセパラブルフ
ラスコに投入してgOCの温度で回転数的J j Or
pmで攪拌しつつ一時間本合した後、91Cで3時間重
合し、ビースツ)IR−H−70を第1表に示す割合で
配合し、へンシエルミキサーで混合した後1シリンダ一
温度コ、l!rCで押出し、ペレット化した◎第   
l   表 次にこの押出ベレットをりjCでコ4’Hre乾た。そ
の結果を第2表にボした。
The above are the essential ingredients and blending ratio of the present invention, but in order to specifically obtain the composition of the present invention, after weighing the above-mentioned resin within the scope of the present invention, use a Henschel mixer or After mixing in a mold blender, it may be pelletized using an extruder, or after dissolving the 1-crosslinked acrylic acid ester yarn body in an impact-resistant resin monomer mixture containing a rubber component,
It can also be obtained by bulk Togane or suspension polymerization.Dyeing and pigments, ultraviolet absorbers, oxidation stabilizers, etc. can be added to the composition of the present invention as required. More specifically, Example 7 to Comparative Example 1 Into a separable flask equipped with a condenser, a stirrer, and a thermometer, methyl methacrylate, nitrate, and obrovil methacrylate were added as a dispersant. Copolymer Q! Add dissolved water 30009 and separate! Ill-ordered methyl methacrylate! A mixture obtained by dissolving 3 g of n-octyl mercaptan and 119 azobisisobutyonitrile in a monomer mixture of 30 g of cyclohexylda metatallylate and 7j9 of butyl acrylate was charged into a separable flask and heated at a temperature of gOC at a rotational speed of J. j Or
After polymerization for 1 hour while stirring at 100 pm, polymerization was carried out at 91C for 3 hours, and Beasts) IR-H-70 was blended in the ratio shown in Table 1, mixed in a Henschel mixer, and then heated in one cylinder at one temperature. ,l! Extruded with rC and pelletized ◎
The extruded pellet was then dried in a vacuum cleaner for 4' hours. The results are shown in Table 2.

□。□.

一へ 実施例3 実施例1と全く同様な方法でメタクリル酸メチルvoo
g、メタクリル酸シクロヘキシルj−s9、メタクリル
!!−−エチルへキシルクSgの単量体混合物を富含さ
せ、得られたポリマー920gと三菱レイヨン(株)族
アクリベット IR−H−り0 109とを■型ブレン
ダーでブレンド後シリンダー島度コ1IOCで押出しペ
レット化した。このボ、リマーの物性を測定し結果を第
3表に示した。
Example 3 In exactly the same manner as in Example 1, methyl methacrylate voo
g, cyclohexyl methacrylate j-s9, methacrylic! ! --Blending 920 g of the obtained polymer with a monomer mixture of ethylhexyl Sg and Mitsubishi Rayon Co., Ltd. Group Acrybet IR-H-RI0 109 in a ■ type blender, and then using a cylinder Shimadoko 1IOC. Extruded into pellets. The physical properties of this reamer were measured and the results are shown in Table 3.

Claims (1)

【特許請求の範囲】 l 単量体成分に換算してメタクリル酸メチル囚s0〜
Sj重量襲、メタクリル酸シタリヘキシルの)/jt−
jO重量外、および(2)および■)と共重合可能な他
のビニル単量体(On−10東量襲とからなる共重合体
中70〜98重量部と架橋アクリル酸エステル系重合体
をゴム成分とした耐衝撃性アクリル樹脂1)2〜30重
量部(合計100重量@)とからなるメタクリル樹脂組
成物〇 ユ 共重合体(1)を構成するビニル単量体(C)が次
素数/ A/Iのアルキル基な有するアルキルアクリレ
ートaコ〜70重量噂な含有する共重合体中であり1情
報記録体成形用に適するものであることを特徴とするI
#詐錆求の範囲゛第1項記載のメタクリル樹脂組成物。
[Claims] l Methyl methacrylate s0~ in terms of monomer components
Sj weight, citalyhexyl methacrylate)/jt-
70 to 98 parts by weight of a copolymer consisting of On-10 and other vinyl monomers (2) and A methacrylic resin composition consisting of impact-resistant acrylic resin as a rubber component 1) 2 to 30 parts by weight (total 100 parts by weight) The vinyl monomer (C) constituting the copolymer (1) is the prime number / A/I is a copolymer containing an alkyl acrylate a having an alkyl group of ~70% by weight, and is suitable for molding information recording bodies.
# Scope of fraud-seeking methacrylic resin composition according to item 1.
JP56204731A 1981-12-18 1981-12-18 Methacrylic resin composition Pending JPS58104939A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56204731A JPS58104939A (en) 1981-12-18 1981-12-18 Methacrylic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56204731A JPS58104939A (en) 1981-12-18 1981-12-18 Methacrylic resin composition

Publications (1)

Publication Number Publication Date
JPS58104939A true JPS58104939A (en) 1983-06-22

Family

ID=16495375

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56204731A Pending JPS58104939A (en) 1981-12-18 1981-12-18 Methacrylic resin composition

Country Status (1)

Country Link
JP (1) JPS58104939A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58162614A (en) * 1982-03-20 1983-09-27 Konishiroku Photo Ind Co Ltd Optical resin composition and optical element
EP0321878A2 (en) * 1987-12-19 1989-06-28 Röhm GmbH Impact modifier for plastic materials
EP0360137A2 (en) * 1988-09-20 1990-03-28 BASF Aktiengesellschaft Transparent thermoplastic blends
US5219935A (en) * 1987-12-19 1993-06-15 Rohm Gmbh Impact modified synthetic resins
AU753160B2 (en) * 2000-05-31 2002-10-10 Ishida Co., Ltd. Load cell
CN114901750A (en) * 2019-07-05 2022-08-12 盛禧奥欧洲有限责任公司 Polymerizable compositions and copolymers of cyclic (meth) acrylates with alkyl (meth) acrylates and/or free-radically polymerizable monomers

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58162614A (en) * 1982-03-20 1983-09-27 Konishiroku Photo Ind Co Ltd Optical resin composition and optical element
EP0321878A2 (en) * 1987-12-19 1989-06-28 Röhm GmbH Impact modifier for plastic materials
JPH01203450A (en) * 1987-12-19 1989-08-16 Roehm Gmbh Impact resistance improving agent for plastic and polymer compound
US5219935A (en) * 1987-12-19 1993-06-15 Rohm Gmbh Impact modified synthetic resins
EP0360137A2 (en) * 1988-09-20 1990-03-28 BASF Aktiengesellschaft Transparent thermoplastic blends
EP0360137A3 (en) * 1988-09-20 1992-04-01 BASF Aktiengesellschaft Transparent thermoplastic blends
AU753160B2 (en) * 2000-05-31 2002-10-10 Ishida Co., Ltd. Load cell
CN114901750A (en) * 2019-07-05 2022-08-12 盛禧奥欧洲有限责任公司 Polymerizable compositions and copolymers of cyclic (meth) acrylates with alkyl (meth) acrylates and/or free-radically polymerizable monomers

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