JP2003292632A - Method for producing acrylic resin plate - Google Patents

Method for producing acrylic resin plate

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Publication number
JP2003292632A
JP2003292632A JP2002100185A JP2002100185A JP2003292632A JP 2003292632 A JP2003292632 A JP 2003292632A JP 2002100185 A JP2002100185 A JP 2002100185A JP 2002100185 A JP2002100185 A JP 2002100185A JP 2003292632 A JP2003292632 A JP 2003292632A
Authority
JP
Japan
Prior art keywords
resin plate
acrylic resin
viscosity
raw material
thickness
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
JP2002100185A
Other languages
Japanese (ja)
Inventor
Hiroki Ishibashi
弘樹 石橋
Yoshiya Kurachi
与志也 倉地
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 JP2002100185A priority Critical patent/JP2003292632A/en
Publication of JP2003292632A publication Critical patent/JP2003292632A/en
Pending legal-status Critical Current

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  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing a resin plate with reduced strain without reducing productivity. <P>SOLUTION: In the method for producing an acrylic resin plate by casting a polymerizable raw material into a casting mold, and polymerizing and curing the polymerizable raw material, the viscosity of the polymerizable raw material is controlled according to the thickness of the acrylic resin plate in such a manner that (1) when the thickness is less than 8 mm, the viscosity is 0.12-0.36 Pas; (2) when the thickness is not less than 8 mm to less than 40 mm, the viscosity is 0.18-0.42 Pas; and (3) when the thickness is not less than 40 mm, the viscosity is 0.48-0.72 Pas. <P>COPYRIGHT: (C)2004,JPO

Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、アクリル樹脂板の
製造方法に関する。 【0002】 【従来の技術】アクリル樹脂板等の樹脂板を製造する方
法として、鋳型に重合性原料を注入して、その鋳型を温
水等に浸漬することによって重合性原料を重合硬化させ
て樹脂板を製造する方法が広く用いられている。アクリ
ル樹脂板はその用途によって、1.5mm等の薄い板か
ら、100mm等の厚い板まで製造されている。 【0003】 【発明が解決しようとする課題】しかしながら、その製
造方法において、薄い板や厚い板を同じ重合性原料を用
いて製造した場合、薄い板では鋳型への注入に時間を要
して生産性を低下させる問題や、鋳型内へ重合性原料を
注入した際の原料の流れた跡が歪となって現れるという
問題があった。一方、厚い板では重合硬化時の加熱によ
って鋳型内での重合性原料が対流し、その対流によって
歪が発生するという問題があった。 【0004】本発明の目的は、生産性を低下させること
無く、歪の少ない樹脂板の製造方法を提供することにあ
る。 【0005】 【課題を解決するための手段】本発明の要旨は、鋳型に
重合性原料を注入して、その重合性原料を重合硬化させ
るアクリル樹脂板の製造方法において、アクリル樹脂板
の厚みによって重合性原料の粘度を下記の粘度とする製
造方法にある。 【0006】 (1)厚みが8mm未満の場合、0.12〜0.36P
a・s (2)厚みが8mm以上40mm未満の場合、0.18
〜0.42Pa・s (3)厚みが40mm以上の場合、0.48〜0.72
Pa・s 【0007】 【発明の実施の形態】本発明の製法で用いる鋳型は、一
対のガラス板、表面を研磨したステンレス板等とガスケ
ットとからなる。 【0008】ガスケットとしては、塩化ビニル樹脂系ガ
スケット、ポリエチレン樹脂系ガスケット、シリコンゴ
ム系ガスケット等が挙げられる。ガスケットの形状とし
ては、断面が中空円形状、角状、丸状、台形状等の形状
が挙げられる。その太さ及び長さは特に限定されるもの
ではなく、製造される樹脂板の厚み及び面積に応じて適
宜変更することができる。 【0009】鋳型に注入される重合性原料は、メタクリ
ル酸メチル(以下、適宜「MMA」という)を70質量
%以上含有するものが好ましい。その他の重合性原料と
してはアクリル酸メチル、アクリル酸エチル等のアクリ
ル酸エステルや、メタクリル酸エチル等のMMA以外の
メタクリル酸エステルや、メタクリル酸等が挙げられ
る。重合性原料の粘度は、製造されるアクリル樹脂板の
厚みによって決まる。アクリル樹脂板の厚みが8mm未
満の場合、重合性原料の粘度は0.12〜0.36Pa
・sである。0.20〜0.28Pa・sが好ましい。
アクリル樹脂板の厚みの下限は、1.5mmであること
が好ましい。 【0010】アクリル樹脂板の厚みが8mm以上40m
m未満の場合、重合性原料の粘度は、0.18〜0.4
2Pa・sである。0.26〜0.34Pa・sが好ま
しい。 【0011】アクリル樹脂板の厚みが40mm以上の場
合、重合性原料の粘度は、0.48〜0.72Pa・s
である。0.56〜0.64Pa・sが好ましい。樹脂
板の厚みの上限は100mmであることが好ましい。 【0012】重合性原料の粘度を調製する方法として
は、MMAに2,2’−アゾビスイソブチロニトリル等
の重合開始剤を添加して、その一部を重合させることに
よって、重合体の分子量と重合率とを調製することによ
って、重合性原料の粘度を調製する方法が挙げられる。
実際の生産においては、予め複数の粘度に調製した重合
性原料を準備し、それらを混合して使用することもでき
る。 【0013】重合性原料を重合させるためには、重合性
原料に2,2’−アゾビスイソブチロニトリル、2,
2’−アゾビス(2,4−ジメチルバレロニトリル)、
2,2’−アゾビス(4−メトキシ2,4−ジメチルバ
レロニトリル)、1,1’−アゾビス(シクロヘキサン
−1−カルボニトリル)等のアゾ系重合開始剤や、ラウ
ロイルパーオキサイド、メチルエチルケトンパーオキサ
イド、ジイソプロピルパーオキシジカーボネート、ジシ
クロヘキサンパーオキシジカーボネート等の過酸化物系
重合開始剤等を含有させることが好ましい。 【0014】また、本発明の樹脂板の製板方法において
は、必要に応じて重合性原料中に紫外線吸収剤、酸化防
止剤、離型剤等の種々の公知の添加剤を含有させること
ができる。 【0015】重合性原料を重合硬化させるには、熱媒と
して水または空気を用いて20℃〜80℃、好ましくは
30℃〜65℃の温度範囲で重合硬化させることが好ま
しい。重合時間は0.5〜200時間であることが好ま
しい。 【0016】この重合の後、熱風炉内において100℃
〜140℃、好ましくは120℃〜135℃の温度範囲
で、さらに重合させることが好ましい。その重合時間は
1時間以上であることが好ましい。 【0017】重合性原料を重合硬化させた後に、鋳型か
ら板状重合体を剥離させて樹脂板を取り出すことができ
る。 【0018】 【実施例】(1)粘度の測定方法 JIS K 7117−1に準じて、重合性原料につい
て、株式会社東京計器製造所製のB型粘度計を用いて粘
度を測定した。 【0019】(2)重合率の測定方法 重合性原料をノルマルヘキサンからなる溶媒に入れて、
溶媒に不溶の重合体と溶媒に可溶の単量体とをろ紙によ
りろ過することで分離した後、ろ紙上の重合体を乾燥し
溶媒を除去することで重合体のみを取り出し、重合性原
料の質量をMとし、分離された重合体の質量をaとする
ことによって、重合率Xをa/M×100(質量%)か
ら求めた。 【0020】(3)重量平均分子量の測定方法 重合性原料をテトロヒドロフランに溶解して、東ソー
(株)製ゲルパーミエイションクロマトグラフィーHP
LC−8120GPCを用いて測定した。カラムにはT
SK−GEL SUPER HM−H 6.0mmφ×
150mmを、ガードカラムにはTSK−GUARDC
OLUMN SUPER H−H 4.6mmφ×35
mmを用いた。検量線用標準ポリマーにはポリスチレン
を使用した。 【0021】(4)得られた樹脂板の歪み測定 手前に投影機を設置し、投影機から4m離れた位置にア
クリル樹脂板を設置した。アクリル樹脂板の更に1m後
方にアクリル樹脂板と平行にスクリーンを設置し、投影
機から投影された光がアクリル樹脂板を透過してスクリ
ーンに映し出され、その映し出された光の濃淡を観察す
ることによって、アクリル樹脂板中の歪みの有無を判断
した。即ち、スクリーン上の光に濃淡がないアクリル樹
脂板は歪みが無く、光に濃淡があるアクリル樹脂板は歪
みがあると判断した。 【0022】[実施例1]外径8.5mm、肉厚2mm
の塩化ビニル製の無端ガスケットを介して、大きさ12
00mm×1200mm×10mmの2枚の強化ガラス
板を積層して鋳型を形成した。 【0023】発生蒸気の冷却管付きSUS製重合容器内
で、MMAを加温し、MMAの温度が75℃に達したと
き、MMA100質量部に対して2,2’−アゾビスイ
ソブチロニトリル0.0022質量部を添加し、さらに
加温を継続してMMAの温度が95℃に達した時点で加
温を停止した。加温を停止した状態で10分保持した
後、重合容器を氷水に入れて常温まで冷却した。得られ
た重合性原料(1)の粘度は0.12Pa・sであり、
重合率は6質量%であり、重合体の重量平均分子量は8
00,000であった。 【0024】2,2’−アゾビスイソブチロニトリルの
添加量を0.0006質量部とし、保持時間を20分と
したこと以外は上述と同様な方法で重合を行った。得ら
れた重合性原料(2)の粘度は0.6Pa・sであり、
重合率は7質量%であり、重合体の重量平均分子量は
2,400,000であった。 【0025】次いで、粘度0.12Pa・sの重合性原
料(1)60質量部と粘度0.6Pa・sの重合性原料
(2)40質量部とを均一に撹拌して、その混合物10
0質量部に対し、重合開始剤として2,2’−(2,4
−ジメチルバレロニトリル)0.01質量部、離型剤と
してエアロゾールOT(アメリカンシアナミド社製)
0.02質量部を添加し、再度、均一に攪拌し、粘度
0.24Pa・sの重合性原料を得た。 【0026】鋳型の中にこの重合性原料を9100g注
入した。鋳型への注入に要した時間は40秒であった。
重合初期に65℃の水浴槽において、3時間重合した。
次いで125℃の空気浴槽において3時間重合し、鋳型
から板状重合体を剥離させて、板厚5mmのアクリル樹
脂板を得た。 【0027】[実施例2]外径41mm、肉厚7mmの
塩化ビニル製の無端ガスケットを介して、大きさ120
0mm×1200mm×10mmの2枚の強化ガラス板
を積層して鋳型を形成した。 【0028】次いで、粘度0.6Pa・sの重合性原料
(2)90質量部とMMA10質量部とを均一に撹拌し
て、その混合物100質量部に対して、重合開始剤とし
て2,2−アゾビス(4−メトキシ2,4−ジメチルバ
レロニトリル)0.0035質量部、離型剤としてエア
ロゾールOT(アメリカンシアナミド社製)0.02質
量部を添加し、均一に攪拌し、粘度0.3Pa・sの重
合性原料を得た。その重合性原料を鋳型の中に5130
0g注入した。鋳型への注入に要した時間は62秒であ
った。重合初期に40℃の水浴槽において、20時間重
合した後、65℃の水浴槽で3時間重合し、次いで95
℃の空気浴槽において2時間重合した後、125℃の空
気浴槽において3時間重合し、鋳型から板状重合体を剥
離させて、板厚30mmのアクリル樹脂板を得た。 【0029】[実施例3]外径68mm、肉厚11mm
の塩化ビニル製の無端ガスケットを介して、大きさ12
00mm×1200mm×10mmの2枚の強化ガラス
板を積層して鋳型を形成した。 【0030】次いで、粘度0.6Pa・sの重合性原料
(2)100質量部に対し、重合開始剤として2,2−
アゾビス(4−メトキシ2,4−ジメチルバレロニトリ
ル)0.0015質量部、離型剤としてエアロゾールO
T(アメリカンシアナミド社製)0.02質量部を添加
し、均一に攪拌した。攪拌後の重合性原料の粘度は0.
6Pa・sであった。その重合性原料を、鋳型の中に8
6500g注入した。鋳型への注入に要した時間は48
秒であった。重合初期に40℃の水浴槽において、62
時間重合し、次いで70℃の空気浴槽で3時間重合した
後、95℃の空気浴槽において2時間、125℃の空気
浴槽において3時間重合し、鋳型から板状重合体を剥離
させて、板厚50mmのアクリル樹脂板を得た。 【0031】[比較例1]混合比を変えて、0.6Pa
・sの粘度に調製した重合性原料を用いたこと以外は実
施例1と同様にして、アクリル樹脂板を製造した。鋳型
への注入に要した時間は276秒であった。 【0032】[比較例2]混合比を変えて、0.03Pa
・sの粘度に調製した重合性原料を用いたこと以外は実
施例2と同様にして、アクリル樹脂板を製造した。一組
の鋳型への注入に要した時間は32秒であった。 【0033】実施例1、実施例2、実施例3、比較例
1、比較例2で得たアクリル樹脂板の歪みを測定した。 【0034】実施例1〜実施例3で製造されたアクリル
樹脂板を透過した光には濃淡はなく、歪みのないアクリ
ル樹脂板であった。 【0035】比較例1で製造されたアクリル樹脂板を透
過した光には濃淡があり、歪みのあるアクリル樹脂板で
あった。 【0036】比較例2で製造したアクリル樹脂板を透過
した光には濃淡があり、歪みのあるアクリル樹脂板であ
った。 【0037】 【発明の効果】本発明の樹脂板の製造方法によって、生
産性を低下させること無く、歪みの少ないアクリル樹脂
板を提供することができる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an acrylic resin plate. 2. Description of the Related Art As a method for producing a resin plate such as an acrylic resin plate, a polymerizable material is poured into a mold, and the polymerizable material is polymerized and cured by immersing the mold in warm water or the like. Plate manufacturing methods are widely used. The acrylic resin plate is manufactured from a thin plate such as 1.5 mm to a thick plate such as 100 mm depending on the use. [0003] However, in the manufacturing method, when a thin plate or a thick plate is manufactured using the same polymerizable raw material, the thin plate requires a long time to be poured into a mold. There is a problem that the properties of the polymerizable material are reduced, and a trace of the flow of the raw material when the polymerizable raw material is injected into the mold is distorted. On the other hand, in the case of a thick plate, there is a problem that the polymerizable raw material in the mold convects due to heating during the polymerization curing, and the convection causes distortion. An object of the present invention is to provide a method for producing a resin plate having less distortion without lowering productivity. SUMMARY OF THE INVENTION The gist of the present invention is to provide a method for producing an acrylic resin plate by injecting a polymerizable material into a mold and polymerizing and curing the polymerizable material. In the production method, the viscosity of the polymerizable raw material is set to the following viscosity. (1) When the thickness is less than 8 mm, 0.12 to 0.36P
a · s (2) When the thickness is 8 mm or more and less than 40 mm, 0.18
(0.4) 0.48 to 0.72 when the thickness is 40 mm or more.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS A mold used in the production method of the present invention comprises a pair of glass plates, a stainless steel plate whose surface is polished, and a gasket. Examples of the gasket include a vinyl chloride resin gasket, a polyethylene resin gasket, and a silicone rubber gasket. Examples of the shape of the gasket include a cross section having a hollow circular shape, a square shape, a round shape, a trapezoidal shape, and the like. The thickness and length are not particularly limited, and can be appropriately changed according to the thickness and area of the manufactured resin plate. The polymerizable raw material injected into the mold preferably contains at least 70% by mass of methyl methacrylate (hereinafter referred to as "MMA" as appropriate). Other polymerizable raw materials include acrylates such as methyl acrylate and ethyl acrylate, methacrylates other than MMA such as ethyl methacrylate, and methacrylic acid. The viscosity of the polymerizable material depends on the thickness of the acrylic resin plate to be manufactured. When the thickness of the acrylic resin plate is less than 8 mm, the viscosity of the polymerizable raw material is 0.12 to 0.36 Pa
-It is s. 0.20 to 0.28 Pa · s is preferable.
The lower limit of the thickness of the acrylic resin plate is preferably 1.5 mm. The thickness of the acrylic resin plate is 8 mm or more and 40 m
m, the viscosity of the polymerizable raw material is 0.18 to 0.4.
2 Pa · s. 0.26 to 0.34 Pa · s is preferable. When the thickness of the acrylic resin plate is 40 mm or more, the viscosity of the polymerizable raw material is 0.48 to 0.72 Pa · s.
It is. 0.56 to 0.64 Pa · s is preferable. The upper limit of the thickness of the resin plate is preferably 100 mm. As a method of adjusting the viscosity of the polymerizable raw material, a polymerization initiator such as 2,2'-azobisisobutyronitrile is added to MMA, and a part of the polymerization initiator is polymerized. There is a method of adjusting the viscosity of the polymerizable raw material by adjusting the molecular weight and the polymerization rate.
In actual production, it is also possible to prepare polymerizable raw materials which have been adjusted to a plurality of viscosities in advance, and to mix and use them. In order to polymerize the polymerizable raw material, 2,2′-azobisisobutyronitrile,
2′-azobis (2,4-dimethylvaleronitrile),
Azo polymerization initiators such as 2,2′-azobis (4-methoxy 2,4-dimethylvaleronitrile) and 1,1′-azobis (cyclohexane-1-carbonitrile), lauroyl peroxide, methyl ethyl ketone peroxide, It is preferable to contain a peroxide polymerization initiator such as diisopropyl peroxydicarbonate and dicyclohexaneperoxydicarbonate. In the method for producing a resin plate of the present invention, various known additives such as an ultraviolet absorber, an antioxidant and a release agent may be contained in the polymerizable raw material, if necessary. it can. In order to polymerize and cure the polymerizable raw material, it is preferable to polymerize and cure at 20 to 80 ° C., preferably 30 to 65 ° C. using water or air as a heat medium. The polymerization time is preferably from 0.5 to 200 hours. After this polymerization, 100 ° C.
It is preferable to further polymerize in a temperature range of from 140 to 140C, preferably from 120C to 135C. The polymerization time is preferably 1 hour or more. After polymerizing and curing the polymerizable raw material, the resin plate can be taken out by peeling the plate-like polymer from the mold. EXAMPLES (1) Method of Measuring Viscosity The viscosity of a polymerizable material was measured using a B-type viscometer manufactured by Tokyo Keiki Seisakusho in accordance with JIS K 7117-1. (2) Method of Measuring Polymerization Rate A polymerizable raw material is put in a solvent composed of normal hexane,
After the polymer insoluble in the solvent and the monomer soluble in the solvent are separated by filtration through a filter paper, the polymer on the filter paper is dried, and the solvent is removed to remove only the polymer, thereby obtaining a polymerizable raw material. The polymerization rate X was determined from a / M × 100 (% by mass) by setting the mass of M to M and the mass of the separated polymer to a. (3) Method of measuring weight average molecular weight A polymerizable raw material is dissolved in tetrahydrofuran, and gel permeation chromatography HP manufactured by Tosoh Corporation is used.
It measured using LC-8120GPC. T in the column
SK-GEL SUPER HM-H 6.0mmφ ×
150 mm, TSK-GUARDC for guard column
OLUMN SUPER H-H 4.6mmφ × 35
mm. Polystyrene was used as the standard polymer for the calibration curve. (4) A projector was set in front of measuring the distortion of the obtained resin plate, and an acrylic resin plate was set at a position 4 m away from the projector. A screen is placed 1 m behind the acrylic resin plate in parallel with the acrylic resin plate, and the light projected from the projector passes through the acrylic resin plate and is projected on the screen, and the light and shade of the projected light is observed. Thus, the presence or absence of distortion in the acrylic resin plate was determined. That is, it was determined that the acrylic resin plate having no shading in the light on the screen had no distortion, and the acrylic resin plate having shading in the light had distortion. [Example 1] Outer diameter 8.5 mm, wall thickness 2 mm
Size 12 through an endless gasket made of vinyl chloride
A mold was formed by laminating two tempered glass plates of 00 mm × 1200 mm × 10 mm. The MMA was heated in a SUS polymerization vessel equipped with a cooling pipe for the generated steam. When the temperature of the MMA reached 75 ° C., 2,2′-azobisisobutyronitrile was added to 100 parts by mass of the MMA. 0.0022 parts by mass was added, and the heating was further continued. When the temperature of the MMA reached 95 ° C., the heating was stopped. After keeping the heating stopped for 10 minutes, the polymerization vessel was put into ice water and cooled to room temperature. The viscosity of the obtained polymerizable raw material (1) is 0.12 Pa · s,
The conversion was 6% by mass, and the weight average molecular weight of the polymer was 8%.
00,000. Polymerization was carried out in the same manner as described above, except that the amount of 2,2'-azobisisobutyronitrile was 0.0006 parts by mass and the holding time was 20 minutes. The viscosity of the obtained polymerizable raw material (2) is 0.6 Pa · s,
The conversion was 7% by mass, and the weight average molecular weight of the polymer was 2,400,000. Next, 60 parts by mass of the polymerizable material (1) having a viscosity of 0.12 Pa · s and 40 parts by mass of the polymerizable material (2) having a viscosity of 0.6 Pa · s are uniformly stirred, and the mixture 10
With respect to 0 parts by mass, 2,2 ′-(2,4
-Dimethylvaleronitrile) 0.01 part by mass, Aerosol OT (manufactured by American Cyanamide Co., Ltd.) as a release agent
0.02 parts by mass was added, and the mixture was uniformly stirred again to obtain a polymerizable material having a viscosity of 0.24 Pa · s. 9100 g of this polymerizable material was injected into the mold. The time required for injection into the mold was 40 seconds.
In the early stage of the polymerization, polymerization was carried out for 3 hours in a water bath at 65 ° C.
Then, polymerization was carried out for 3 hours in an air bath at 125 ° C., and the plate-like polymer was peeled off from the mold to obtain an acrylic resin plate having a thickness of 5 mm. [Example 2] A size of 120 mm was passed through an endless gasket made of vinyl chloride having an outer diameter of 41 mm and a thickness of 7 mm.
A mold was formed by laminating two tempered glass plates of 0 mm × 1200 mm × 10 mm. Next, 90 parts by mass of the polymerizable raw material (2) having a viscosity of 0.6 Pa · s and 10 parts by mass of MMA are uniformly stirred, and 100 parts by mass of the mixture is mixed with 2,2- 0.0035 parts by mass of azobis (4-methoxy 2,4-dimethylvaleronitrile) and 0.02 parts by mass of aerosol OT (manufactured by American Cyanamide Co.) as a release agent were added, and the mixture was stirred uniformly and the viscosity was 0.3 Pa. * The polymerizable raw material of s was obtained. The polymerizable material is placed in a mold in 5130
0 g was injected. The time required for injection into the mold was 62 seconds. In the early stage of polymerization, polymerization was carried out in a water bath at 40 ° C. for 20 hours, then polymerization was carried out for 3 hours in a water bath at 65 ° C.
After polymerizing for 2 hours in an air bath at 125 ° C., polymerizing for 3 hours in an air bath at 125 ° C., the plate polymer was peeled off from the mold to obtain an acrylic resin plate having a thickness of 30 mm. [Example 3] Outer diameter 68 mm, wall thickness 11 mm
Size 12 through an endless gasket made of vinyl chloride
A mold was formed by laminating two tempered glass plates of 00 mm × 1200 mm × 10 mm. Next, 2,100 as a polymerization initiator was added to 100 parts by mass of the polymerizable raw material (2) having a viscosity of 0.6 Pa · s.
0.0015 parts by mass of azobis (4-methoxy 2,4-dimethylvaleronitrile), Aerosol O as a release agent
0.02 parts by mass of T (manufactured by American Cyanamid Co.) was added and stirred uniformly. The viscosity of the polymerizable material after stirring is 0.1.
It was 6 Pa · s. Put the polymerizable material in a mold
6,500 g were injected. The time required for injection into the mold was 48
Seconds. In a water bath at 40 ° C. in the early stage of polymerization, 62
After polymerizing for 3 hours in a 70 ° C. air bath, polymerizing for 2 hours in a 95 ° C. air bath and 3 hours in a 125 ° C. air bath, the plate polymer was peeled from the mold, and the A 50 mm acrylic resin plate was obtained. [Comparative Example 1] The mixing ratio was changed and 0.6 Pa
An acrylic resin plate was manufactured in the same manner as in Example 1 except that the polymerizable raw material adjusted to have a viscosity of s was used. The time required for injection into the mold was 276 seconds. [Comparative Example 2] The mixture ratio was changed to 0.03 Pa
An acrylic resin plate was manufactured in the same manner as in Example 2 except that the polymerizable raw material adjusted to have a viscosity of s was used. The time required for injection into one set of molds was 32 seconds. The distortion of the acrylic resin plates obtained in Example 1, Example 2, Example 3, Comparative Example 1 and Comparative Example 2 was measured. The light transmitted through the acrylic resin plates manufactured in Examples 1 to 3 was an acrylic resin plate having no density and no distortion. The light transmitted through the acrylic resin plate manufactured in Comparative Example 1 was a dark and distorted acrylic resin plate. The light transmitted through the acrylic resin plate produced in Comparative Example 2 was a dark and light, distorted acrylic resin plate. According to the method for producing a resin plate of the present invention, an acrylic resin plate with less distortion can be provided without lowering productivity.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4F071 AA32X AA33 AA33X AA88 AG02 AG32 BA09 BB01 BB12 BC03 BC17 4J100 AJ02P AL03P CA01 CA04 DA09 FA17 FA27 FA47 GC00 GD19    ────────────────────────────────────────────────── ─── Continuation of front page    F term (reference) 4F071 AA32X AA33 AA33X AA88                       AG02 AG32 BA09 BB01 BB12                       BC03 BC17                 4J100 AJ02P AL03P CA01 CA04                       DA09 FA17 FA27 FA47 GC00                       GD19

Claims (1)

【特許請求の範囲】 【請求項1】 鋳型に重合性原料を注入して、その重合
性原料を重合硬化させるアクリル樹脂板の製造方法にお
いて、アクリル樹脂板の厚みによって重合性原料の粘度
を下記の粘度とする製造方法。 (1)厚みが8mm未満の場合、0.12〜0.36P
a・s (2)厚みが8mm以上40mm未満の場合、0.18
〜0.42Pa・s (3)厚みが40mm以上の場合、0.48〜0.72
Pa・s
Claims: 1. A method for producing an acrylic resin plate, in which a polymerizable material is injected into a mold and the polymerizable material is polymerized and cured, wherein the viscosity of the polymerizable material is determined according to the thickness of the acrylic resin plate. Production method for obtaining a viscosity of (1) When the thickness is less than 8 mm, 0.12 to 0.36P
a · s (2) When the thickness is 8 mm or more and less than 40 mm, 0.18
(0.4) 0.48 to 0.72 when the thickness is 40 mm or more.
Pa · s
JP2002100185A 2002-04-02 2002-04-02 Method for producing acrylic resin plate Pending JP2003292632A (en)

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JP2002100185A JP2003292632A (en) 2002-04-02 2002-04-02 Method for producing acrylic resin plate

Publications (1)

Publication Number Publication Date
JP2003292632A true JP2003292632A (en) 2003-10-15

Family

ID=29241264

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2003292632A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020084150A (en) * 2018-11-30 2020-06-04 株式会社クラレ Methacrylic resin cast plate and method for producing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020084150A (en) * 2018-11-30 2020-06-04 株式会社クラレ Methacrylic resin cast plate and method for producing the same
JP7166154B2 (en) 2018-11-30 2022-11-07 株式会社クラレ Methacrylic resin cast plate and method for producing the same

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