JPH04254928A - Methacrylic resin for optical information recording medium - Google Patents
Methacrylic resin for optical information recording mediumInfo
- Publication number
- JPH04254928A JPH04254928A JP3016364A JP1636491A JPH04254928A JP H04254928 A JPH04254928 A JP H04254928A JP 3016364 A JP3016364 A JP 3016364A JP 1636491 A JP1636491 A JP 1636491A JP H04254928 A JPH04254928 A JP H04254928A
- Authority
- JP
- Japan
- Prior art keywords
- methacrylic resin
- methyl methacrylate
- information recording
- resin
- optical information
- 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
- 239000000113 methacrylic resin Substances 0.000 title claims abstract description 16
- 230000003287 optical effect Effects 0.000 title abstract description 16
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 17
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000011347 resin Substances 0.000 abstract description 7
- 229920005989 resin Polymers 0.000 abstract description 7
- 239000000758 substrate Substances 0.000 abstract description 5
- 239000000155 melt Substances 0.000 abstract description 2
- 230000002542 deteriorative effect Effects 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 description 15
- 238000001746 injection moulding Methods 0.000 description 6
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 5
- 230000007423 decrease Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000006082 mold release agent Substances 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- PNOXUQIZPBURMT-UHFFFAOYSA-M potassium;3-(2-methylprop-2-enoyloxy)propane-1-sulfonate Chemical compound [K+].CC(=C)C(=O)OCCCS([O-])(=O)=O PNOXUQIZPBURMT-UHFFFAOYSA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Optical Record Carriers And Manufacture Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、ビデオディスク等の光
学式情報記録体用として有用なメタクリル樹脂に関する
ものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a methacrylic resin useful for optical information recording media such as video discs.
【0002】0002
【従来の技術】メタクリル樹脂は成形性、透明性に優れ
、有用な光学特性を示すため、種々の光学機器として使
用できることが知られており、最近はその優れた性質を
生かしてビデオディスク等の光学式情報記録体用基板と
して使用されている。[Prior Art] Methacrylic resin has excellent moldability and transparency, and exhibits useful optical properties, so it is known that it can be used in various optical devices.Recently, its excellent properties have been used to make video discs, etc. Used as a substrate for optical information recording media.
【0003】光学式情報記録体用基板としては光学歪が
小さく、優れた耐熱性と成形性を併せ持つことが要求さ
れる上、近年、ビデオディスクの生産性の向上、即ち成
形サイクルの短縮が強く望まれている。Substrates for optical information recording media are required to have low optical distortion, excellent heat resistance, and moldability, and in recent years, there has been a strong desire to improve the productivity of video discs, that is, to shorten the molding cycle. desired.
【0004】光学式情報記録体用メタクリル樹脂として
、メチルメタクリレートとエチルメタクリレートの共重
合体(特開昭57ー123208号)が提案されている
。A copolymer of methyl methacrylate and ethyl methacrylate (Japanese Unexamined Patent Publication No. 123208/1983) has been proposed as a methacrylic resin for optical information recording media.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、上記の
共重合体は流動性を向上させると光学歪は減少するが、
その反面、耐熱性が低下したり、機械的強度が低下する
という欠点が出てくるため、生産性を向上させることは
困難であった。[Problems to be Solved by the Invention] However, when the fluidity of the above-mentioned copolymer is improved, the optical distortion decreases;
On the other hand, it has been difficult to improve productivity because of the disadvantages of reduced heat resistance and reduced mechanical strength.
【0006】現在、光学式情報記録体用基板、特に、ビ
デオディスク、オーディオディスクは主に射出成形によ
り製造されているが、その生産性を考慮した場合、樹脂
の耐熱性および流動性により、その成形サイクルが決定
されている。射出成形性における生産性向上のためには
、光学歪が小さく、優れた透明性、機械的強度を損なう
ことなく、樹脂の流動性および射出成形時における冷却
時間の短縮の目的で耐熱性を向上させる必要があるが、
既存の成形材料では耐熱性を向上させると、流動性の低
下や機械的強度の低下を伴うという問題を有している。Currently, optical information recording substrates, especially video disks and audio disks, are mainly manufactured by injection molding, but when considering the productivity, the heat resistance and fluidity of the resin make it difficult to The molding cycle has been determined. In order to improve productivity in injection molding, optical distortion is small, excellent transparency, and heat resistance is improved to reduce resin fluidity and cooling time during injection molding without sacrificing mechanical strength. It is necessary to let
Existing molding materials have a problem in that improving their heat resistance is accompanied by a decrease in fluidity and mechanical strength.
【0007】[0007]
【課題を解決するための手段】そこで、本発明者らはこ
のような現状に鑑み、上述の問題点のない光学式情報記
録体用の材料を提供することにつき鋭意検討した結果、
本発明に到達した。[Means for Solving the Problems] In view of the current situation, the inventors of the present invention have conducted intensive studies to provide a material for optical information recording media that does not have the above-mentioned problems.
We have arrived at the present invention.
【0008】即ち、本発明はメチルメタクリレート単位
80〜99.5重量%およびイソボルニルアクリレート
単位20〜0.5重量%からなる情報記録体用メタクリ
ル樹脂である。That is, the present invention is a methacrylic resin for information recording media comprising 80 to 99.5% by weight of methyl methacrylate units and 20 to 0.5% by weight of isobornyl acrylate units.
【0009】本発明のメタクリル樹脂の共重合比率は上
記の通りであり、この範囲外では成形品の機械的強度、
および量産時の生産性を併せ持つことができない。即ち
、メチルメタクリレート単位が99.5重量%を超える
と樹脂の流動性を維持するために分子量を低くしなけれ
ばならず、その結果、機械的強度が低下する。一方、イ
ソボルニルアクリレート単位が20重量%を超えると機
械的強度に著しく劣ったものとなる。The copolymerization ratio of the methacrylic resin of the present invention is as described above, and outside this range, the mechanical strength of the molded article
It is not possible to combine this with productivity during mass production. That is, if the content of methyl methacrylate units exceeds 99.5% by weight, the molecular weight must be lowered in order to maintain the fluidity of the resin, resulting in a decrease in mechanical strength. On the other hand, if the isobornyl acrylate unit content exceeds 20% by weight, the mechanical strength will be significantly inferior.
【0010】また、本発明のメタクリル樹脂のメルトフ
ローレート(MFR)はASTM−D1238に基づき
荷重3.8kgで測定した値で0.5〜50g/10分
の範囲にあることが好ましい。MFRが0.5g/10
分より小さいと金型からの情報の転写性が劣り、尚且つ
成形品の光学歪が大きくなり、一方50g/10分より
大きいと機械的強度が低下する傾向にある。Further, the melt flow rate (MFR) of the methacrylic resin of the present invention is preferably in the range of 0.5 to 50 g/10 min as measured under a load of 3.8 kg based on ASTM-D1238. MFR is 0.5g/10
If it is smaller than 50 g/10 min, the transferability of information from the mold will be poor and the optical distortion of the molded product will increase, while if it is larger than 50 g/10 min, the mechanical strength will tend to decrease.
【0011】また、本発明のメタクリル樹脂の熱変形温
度は、成形時および使用時の熱変形を考慮すると、AS
TM−D648に基づき荷重18.56kgで測定した
値で70℃以上が好ましく、より好ましくは80℃以上
である。熱変形温度が70℃より低い場合には成形品の
耐熱性に劣り、特に成形時および使用時の熱変形が大き
くなり好ましくなくなる場合がある。[0011] Furthermore, the heat deformation temperature of the methacrylic resin of the present invention is AS
The temperature is preferably 70°C or higher, more preferably 80°C or higher, as measured under a load of 18.56 kg based on TM-D648. If the heat distortion temperature is lower than 70°C, the heat resistance of the molded product will be poor, and in particular, heat distortion during molding and use will become large, which may be undesirable.
【0012】本発明のメタクリル樹脂の製造には、懸濁
重合、塊状重合、溶液重合等のメタクリル樹脂の製造の
慣用法を用いることができる。本発明のメタクリル樹脂
には、必要に応じて安定剤、離型剤、滑剤、可塑剤、染
料等を添加することもできるFor producing the methacrylic resin of the present invention, conventional methods for producing methacrylic resins such as suspension polymerization, bulk polymerization, and solution polymerization can be used. Stabilizers, mold release agents, lubricants, plasticizers, dyes, etc. can also be added to the methacrylic resin of the present invention, if necessary.
【0013】このようにして得られた本発明のメタクリ
ル樹脂は、射出成形、圧縮成形いずれの方法でも基板に
成形できる。The methacrylic resin of the present invention thus obtained can be molded into a substrate by either injection molding or compression molding.
【0014】[0014]
【実施例】以下、実施例により、本発明を具体的に説明
する。なお、実施例中の「部」は「重量部」を示す。な
お、各物性値の測定は、次の方法で行った。
■熱変形温度(HDT)
ASTM−D648に準じて荷重18.56kgで測定
した。
■メルトフローレート(MFR)
ASTM−D1238に準じて荷重3.8kgで測定し
た。
■引張強度、引張伸度
射出成形機(日精樹脂製、PS−60E)によりダンベ
ルA型試験片を射出成形し、ASTM−D638に準じ
て測定した。
■光線透過率
射出成形機(名機製作所製、M−200ダイナメルタ)
によりφ300mmのディスク(1.2mmt)をシリ
ンダー温度260℃で射出成形し、得られたディスク成
形品の中心より7cmの地点の透過率を島津製作所製;
UV−160Aにより500〜900nmの領域で測定
した。
■複屈折
■で得られたディスク成形品の中心より7cmの地点の
複屈折を偏光顕微鏡(Nikon,OPTIPHOT−
POL、SENARMONT COMPENSATO
R:使用波長546nm、single pass)
により測定した。[Examples] The present invention will be specifically explained below with reference to Examples. Note that "parts" in the examples indicate "parts by weight." In addition, the measurement of each physical property value was performed by the following method. ■Heat distortion temperature (HDT) Measured under a load of 18.56 kg according to ASTM-D648. ■Melt flow rate (MFR) Measured under a load of 3.8 kg according to ASTM-D1238. (2) Tensile strength and tensile elongation A dumbbell type test piece was injection molded using an injection molding machine (PS-60E, manufactured by Nissei Plastics Co., Ltd.), and measured according to ASTM-D638. ■Light transmittance injection molding machine (M-200 Dynamelta, manufactured by Meiki Seisakusho)
A φ300 mm disk (1.2 mmt) was injection molded at a cylinder temperature of 260°C, and the transmittance at a point 7 cm from the center of the obtained disk molded product was measured using Shimadzu Corporation;
It was measured in the region of 500 to 900 nm using UV-160A. ■Birefringence■ Birefringence at a point 7 cm from the center of the disc molded product obtained using a polarizing microscope (Nikon, OPTIPHOT-
POL, SENARMONT COMPENSATO
R: Usage wavelength 546nm, single pass)
It was measured by
【0015】実施例1〜4
表1に示す割合のメチルメタクリレートとイソボルニル
アクリレートの単量体混合物100部に、n−オクチル
メルカプタン0.35部を溶解し、重合触媒としてラウ
ロイルパーオキサイド0.44部、離型剤としてステア
リルアルコール0.1部、懸濁重合分散剤としてメタク
リル酸メチルと3−メタクリロイルオキシプロパンスル
ホン酸カリウムの共重合体0.01部、硫酸ナトリウム
0.15部、分散媒として水145部を攪拌機および温
度計の付いたガラス製フラスコ重合装置に混入し、80
℃で重合させて内温がピークに達した後95℃で30分
間保持後冷却し、濾過、水洗、乾燥することによりビー
ズ状共重合体を得た。Examples 1 to 4 0.35 parts of n-octyl mercaptan was dissolved in 100 parts of a monomer mixture of methyl methacrylate and isobornyl acrylate in the proportions shown in Table 1, and 0.35 parts of lauroyl peroxide was added as a polymerization catalyst. 44 parts, stearyl alcohol 0.1 part as a mold release agent, 0.01 part copolymer of methyl methacrylate and potassium 3-methacryloyloxypropanesulfonate as a suspension polymerization dispersant, 0.15 part sodium sulfate, dispersion medium 145 parts of water was mixed into a glass flask polymerization apparatus equipped with a stirrer and a thermometer, and 80
After polymerization was carried out at 95° C. and the internal temperature reached a peak, the mixture was kept at 95° C. for 30 minutes, cooled, filtered, washed with water, and dried to obtain a bead-like copolymer.
【0016】得られた共重合体を、40mm押出機(田
辺プラスチック機械社製)にて、240℃で混練しペレ
ット化した。得られたペレットを用いて各種の評価をし
たところ、表1の結果を得た。The obtained copolymer was kneaded and pelletized at 240° C. using a 40 mm extruder (manufactured by Tanabe Plastic Machinery Co., Ltd.). When the obtained pellets were used for various evaluations, the results shown in Table 1 were obtained.
【0017】なお、光線透過率はいずれの実施例におい
ても500〜900nmの波長領域で91%以上であり
、また、複屈折はいずれも20nm以下と良好であった
。The light transmittance was 91% or more in the wavelength range of 500 to 900 nm in all Examples, and the birefringence was 20 nm or less, which was good.
【0018】比較例1〜4
メチルメタクリレートとエチルアクリレートまたはイソ
ボルニルアクリレートとの表1に示す割合からなる単量
体混合物100重量部を使用した以外は実施例1と全く
同様に実験を行った。なお、比較例4はn−オクチルメ
ルカプタンの使用量を0.62部として行った。結果を
表1に示す。Comparative Examples 1 to 4 Experiments were carried out in exactly the same manner as in Example 1, except that 100 parts by weight of a monomer mixture of methyl methacrylate and ethyl acrylate or isobornyl acrylate in the proportions shown in Table 1 was used. . In Comparative Example 4, the amount of n-octyl mercaptan used was 0.62 parts. The results are shown in Table 1.
【0019】なお、イソボルニルアクリレート30部と
メチルメタクリレート70部を共重合して得られた共重
合体(比較例3)は、機械的強度が弱いため実用性に欠
け、また、メチルメタクリレート100部を重合して得
られた重合体(比較例4)は、MFRが22.5g/1
0分であり、実施例2とほぼ同等の流動性であるが、引
張強度が半分以下であり実用性に欠けるものであった。[0019] The copolymer obtained by copolymerizing 30 parts of isobornyl acrylate and 70 parts of methyl methacrylate (Comparative Example 3) lacks practicality due to its weak mechanical strength. The polymer obtained by polymerizing the part (Comparative Example 4) had an MFR of 22.5 g/1
0 minutes, and the fluidity was almost the same as in Example 2, but the tensile strength was less than half, and it lacked practicality.
【0020】実施例1〜4及び比較例1〜2の結果より
、MFRとHDTの関係は図1のようになり、例えばM
FRが20g/10分の共重合体を得ようとする場合、
メチルメタクリレートとイソボルニルアクリレートの共
重合体は、メチルメタクリレートとエチルアクリレート
の共重合体よりも、HDTで約7℃向上が認められるこ
とがわかる。From the results of Examples 1 to 4 and Comparative Examples 1 to 2, the relationship between MFR and HDT is as shown in FIG.
When trying to obtain a copolymer with an FR of 20 g/10 min,
It can be seen that the copolymer of methyl methacrylate and isobornyl acrylate exhibits an approximately 7° C. improvement in HDT than the copolymer of methyl methacrylate and ethyl acrylate.
【0021】また、HDTが85℃の共重合体を得よう
とする場合、メチルメタクリレートとイソボルニルアク
リレートの共重合体はメチルメタクリレートとエチルア
クリレートの共重合体よりも、MFRで約12g/10
分の向上が認められ、メチルメタクリレートとイソボル
ニルアクリレートの共重合体は、メチルメタクリレート
とエチルアクリレートの共重合体よりもその成形性は生
産性の意味において良好であるといえる。Furthermore, when trying to obtain a copolymer with an HDT of 85°C, the copolymer of methyl methacrylate and isobornyl acrylate has a MFR of about 12 g/10 compared to the copolymer of methyl methacrylate and ethyl acrylate.
It can be said that the copolymer of methyl methacrylate and isobornyl acrylate has better moldability than the copolymer of methyl methacrylate and ethyl acrylate in terms of productivity.
【0022】[0022]
【表1】[Table 1]
【0023】[0023]
【発明の効果】本発明の光学式情報記録体用メタクリル
樹脂は、メタクリル樹脂が本来持つ優れた光学的特性を
保持したまま、耐熱性に優れ、良流動性で生産性にも優
れた成形材料として好適に使用することができるため、
工業上優れた効果を奏する。[Effects of the Invention] The methacrylic resin for optical information recording media of the present invention is a molding material with excellent heat resistance, good fluidity, and productivity while retaining the excellent optical properties inherent to methacrylic resin. Because it can be suitably used as
It has excellent industrial effects.
【図1】本発明のメタクリル樹脂と、従来のメチルメタ
クリレートとエチルアクリレートとの共重合体の、HD
TとMFRの関係を示すものである。FIG. 1: HD of the methacrylic resin of the present invention and the conventional copolymer of methyl methacrylate and ethyl acrylate.
It shows the relationship between T and MFR.
Claims (1)
.5重量%およびイソボルニルアクリレート単位20〜
0.5重量%からなる情報記録体用メタクリル樹脂。[Claim 1] Methyl methacrylate units 80-99
.. 5% by weight and 20 to 20 isobornyl acrylate units
Methacrylic resin for information recording media consisting of 0.5% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3016364A JPH04254928A (en) | 1991-02-07 | 1991-02-07 | Methacrylic resin for optical information recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3016364A JPH04254928A (en) | 1991-02-07 | 1991-02-07 | Methacrylic resin for optical information recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04254928A true JPH04254928A (en) | 1992-09-10 |
Family
ID=11914275
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3016364A Pending JPH04254928A (en) | 1991-02-07 | 1991-02-07 | Methacrylic resin for optical information recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04254928A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100645833B1 (en) * | 2005-06-27 | 2006-11-14 | 엘지엠엠에이 주식회사 | Optical transparent heat resistant resin |
CN104271663A (en) * | 2012-04-27 | 2015-01-07 | 株式会社可乐丽 | (meth)acrylic resin composition |
US20150284520A1 (en) * | 2012-11-09 | 2015-10-08 | Kuraray Co., Ltd. | Methacrylic resin composition |
CN105111359A (en) * | 2015-09-13 | 2015-12-02 | 长春工业大学 | Preparation method of polymethyl methacrylate copolymer |
-
1991
- 1991-02-07 JP JP3016364A patent/JPH04254928A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100645833B1 (en) * | 2005-06-27 | 2006-11-14 | 엘지엠엠에이 주식회사 | Optical transparent heat resistant resin |
CN104271663A (en) * | 2012-04-27 | 2015-01-07 | 株式会社可乐丽 | (meth)acrylic resin composition |
US20150148508A1 (en) * | 2012-04-27 | 2015-05-28 | Kuraray Co., Ltd. | (meth) acrylic resin composition |
US20150284520A1 (en) * | 2012-11-09 | 2015-10-08 | Kuraray Co., Ltd. | Methacrylic resin composition |
CN105111359A (en) * | 2015-09-13 | 2015-12-02 | 长春工业大学 | Preparation method of polymethyl methacrylate copolymer |
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