JPH07166074A - Transparent antistatic resin composition for melt molding - Google Patents

Transparent antistatic resin composition for melt molding

Info

Publication number
JPH07166074A
JPH07166074A JP5315499A JP31549993A JPH07166074A JP H07166074 A JPH07166074 A JP H07166074A JP 5315499 A JP5315499 A JP 5315499A JP 31549993 A JP31549993 A JP 31549993A JP H07166074 A JPH07166074 A JP H07166074A
Authority
JP
Japan
Prior art keywords
resin
water
resin composition
weight
transparent thermoplastic
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.)
Granted
Application number
JP5315499A
Other languages
Japanese (ja)
Other versions
JP3304573B2 (en
Inventor
Tomohiro Maekawa
智博 前川
Masashi Yamamoto
正志 山本
Michio Fujitaka
理夫 藤高
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 JP31549993A priority Critical patent/JP3304573B2/en
Publication of JPH07166074A publication Critical patent/JPH07166074A/en
Application granted granted Critical
Publication of JP3304573B2 publication Critical patent/JP3304573B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To provide a resin composition which is antistatic and can retain its original transparency even when processed or molded at high temperatures by compounding a transparent thermoplastic resin with a water-absorbing resin having a urethane bond. CONSTITUTION:100 pts.wt. of a transparent thermoplastic resin is compounded with 0.1-10 pts.wt. of a water-absorbing resin having a urethane bond and a water absorbing capacity of 10-100g per gram of resin of obtain a resin composition. As the transparent thermoplastic resin, acrylic resins are preferable. The water-absorbing resin can be obtained by reacting a polyether polyol with a compound having an isocyanate group. A preferable polyether polyol is polyethylene glycol because of its excellent water absorbing capacity. Usable isocyanat compounds are those having two or more isocyanate groups in the molecule (e.g. tetramethylene disocyanated). The molar ratio of the polyether polyol to the isocyanate compound is so adjusted that a desired water absorbing capacity can be attained, for example, 70/30-50/50.

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は、耐熱安定性、帯電防止
性に優れた、溶融成形用透明熱可塑性樹脂組成物に関す
るものである。 【0002】 【従来の技術】メタクリル系樹脂、スチレン系樹脂およ
びポリカーボネートは優れた透明性および美麗な外観で
知られており、看板あるいは各種装飾品などに使用され
ている。しかし、これらの樹脂は、静電気が帯電しやす
く、光沢を低下させたり、ほこり等が付着して汚れやす
く、外観が損なわれるのが問題となっている。この問題
に対して、アルキルスルホン酸塩や高級脂肪酸モノグリ
セライドやポリエーテルエステルアミドをメタクリル系
樹脂に混在させる技術が数多く提案されている。例えば
特開平3-122165号公報には、透明性樹脂にアルカリ金属
塩を0.01重量%以上20重量%及びポリエーテル系
高分子体を0.5重量%以上60%以下含有した導電性
樹脂組成物が開示されている。特公平4-98号公報には、
透明性高分子材料にアルキルアリールスルホン酸リチウ
ム塩を30〜10重量%、非イオン界面活性剤70〜9
0重量%からなる帯電防止剤を0.5〜10重量%添加
し、溶融混錬し、透明高分子材料を得る旨が記載されて
いる。 【0003】 【発明が解決しようとする課題】特開平3-122165号公報
記載の組成物は、溶融成形を行うと、含まれるポリエー
テル系高分子体の分解が起こり、着色したり、帯電防止
性能が低下することが多い。特公平4-98号公報記載の組
成物は、比較的低分子量の剤を使用しているため、該組
成物を溶融して成形すると気化して減少し、帯電防止性
能が低下する。 【0004】そこで本発明は、樹脂組成物を射出成形や
押出成形のような溶融成形に供しても透明性と帯電防止
性に優れた樹脂組成物を提供するものである。 【0005】 【課題を解決するための手段】本発明は、透明熱可塑性
樹脂100重量部とウレタン結合を有する吸水性樹脂
0.1〜10重量部とからなる溶融成形用透明帯電防止
性樹脂組成物を提供するものである。 【0006】本発明で用いられる透明熱可塑性樹脂と
は、例えばポリエチレン、ポリプロピレン、エチレン−
酢酸ビニル共重合体、エチレン−メタアクリル酸メチル
共重合体等のポリオレフィン樹脂;ポリメチルメタアク
リレートが主成分のアクリル系樹脂;スチレン系樹脂;
塩化ビニル樹脂;ポリエステル樹脂;ポリアセタール樹
脂;ポリアミド樹脂;ポリカーボネード;ポリイミド樹
脂等が挙げられる。これらの合成樹脂を単独で、もしく
は混合物で、透明性の高いものが該当する。なかでも、
透明性の良いものとしてアクリル樹脂、スチレン樹脂、
ポリカーボネート等が望ましい。さらに好ましくは、ア
クリル系樹脂である。 【0007】該アクリル系樹脂とは、メタクリル酸メチ
ル単独合体あるいはメタクリル酸メチルを50重量%以
上含み、メタクリル酸メチルと共重合性単量体、例えば
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、メタクリル酸フェニル、メタクリル
酸ベンジル、メタクリル酸2−エチルヘキシル、メタク
リル酸2−ヒドロキシエチル、などのメタクリル酸エス
テル類、アクリル酸メチル、アクリル酸エチル、アクリ
ル酸ブチル、アクリルー酸シクロヘキシル、アクリル酸
フェニル、アクリル酸ベンジル、アクリル酸2−エチル
ヘキシル、アクリル酸2−ヒドロキシエチル、などのア
クリル酸エステル類、メタクリル酸、アクリル酸などの
不飽和脂肪酸類、スチレン、α−メチルスチレン、アク
リロニトリル、メタクリロニトリル、無水マレイン酸、
フェニルマレイミド、シクロヘキシルマレイミドなどと
の共重合体であるが、これらに限定されるものではな
い。また、ポリブタジエン、ポリアクリル酸ブチル共重
合体などのエラストマー成分や無水グルタル酸単位、グ
ルタルイミド単位をさらに含んでも良い。 【0008】本発明におけるウレタン結合を有する吸水
性樹脂とは、ポリエーテルポリオールとイソシアネート
基を有する化合物との反応によって得られるものであ
る。 【0009】ポリエーテルポリオールとしては、ポリエ
チレングリコール、ポリプロピレングリコールポリテト
ラメチレングリコール等で、分子内にエーテル結合が1
00個以下のものである。該ポリエーテルポリオールの
中でもポリエチレングリコールが吸水能がより優れてい
る。 【0010】尚、ポリエーテルポリオールの他にその他
のポリオールを、全ポリオール中30%未満を合わせ、
または共縮合して用いることが出来る。このポリオール
としては、ポリテトラメチレンカーボネートジオール、
ポリヘキサメチレンカーボネートジオール等のポリカー
ボネートポリオール類;ポリカプロラクトンジオールの
ごときポリエステルポリオール類がある。 【0011】また、イソシアネート基を有する化合物と
しては、分子内にイソシアネート基が2個以上存在する
ものが使用できる。例としては、テトラメチレンジイソ
シアネート、ヘキサメチレンジイソシアネート、オクタ
メチレンジイソシアネート、トリレンジイソシアネー
ト、4,4−ジフェニルメタンジイソシアネート、キシ
リレンジイソシアネート、リジンジイソシアネート、
4,4−メチレンビス(シクロヘキシルイソシアネー
ト)、メチルシクロヘキサン−2,4(2,6)−ジイ
ソシアネート、 イソホロンジイソシアネート、1.3
−または1.4−ビス(イソシアネートメチル)シクロ
ヘキサン、トリメチルヘキサメチレンジイソシアネー
ト、スルホニルジイソシアネート等、及び上記のイソシ
アネート化合物から得られたイソシアヌレート化合物等
も該当する。 【0012】ポリエーテルポリオール及びイソシアネー
ト基を有する化合物のモル比は、目標の吸水能に合わせ
て調節すれば良い。具体的にはポリエーテルポリオール
/イソシアネート基を有する化合物=70/30〜50
/50のモル比、好ましくは60/40〜50/50
で、ポリエーテルポリオールの比率が高い程吸水能が高
くなる。 【0013】吸水性樹脂の吸水能は10〜100g水/
g樹脂である。10g水/g樹脂未満であると、帯電防
止性能が発現しにくく、100g水/g樹脂を越えるも
のは、長期間放置で樹脂が変質することがある。 【0014】該吸水性樹脂の量は、透明熱可塑性樹脂1
00重量部当り0.1〜10重量部である。中でも0.
5〜5重量部が好ましい。添加量が0.1重量部より少
ないと、充分な帯電防止性は発現せず10重量部より多
いと耐熱性が低下するだけでなく透明熱可塑性樹脂と相
溶しにくくなり、組成物が白濁することがある。 【0015】なお、該吸水性樹脂の量は、その吸水能に
よってより好ましくは、吸水能のg水/g樹脂の数値と
透明熱可塑性樹脂100重量部当りの該吸水性樹脂の重
量部の数値の積が1〜200となる量である。 【0016】本発明おける樹脂組成物に、光拡散剤、艶
消し剤、染料、顔料、光安定剤、紫外線吸収剤、酸化防
止剤、補強剤、充填剤、離型剤、難燃剤等周知の添加剤
を加えてもよい。 【0017】さらに所望により有機化合物系の帯電防止
剤を併用してもよい。併用することのできる有機化合物
系の帯電防止剤としては公知のアルキルスルホン酸塩や
高級脂肪酸グリセライド等である。だだし、無機の過塩
素酸塩のごとく無機塩は、吸水性樹脂の熱分解をもたら
すので併用するのは避けた方がよい。 【0018】該、透明熱可塑性樹脂とウレタン結合を有
する吸水性樹脂とから本発明の熱可塑性樹脂組成物とす
る方法としては両者をヘンシェルミキサー、タンブラー
等で機械的に混合し、バンバリーミキサーや一軸、二軸
の押出機で溶融混錬する周知の方法がある。 【0019】なお、本発明に言う溶融成形とは、該熱可
塑性樹脂を該樹脂の融点以上、あるいはガラス転移温度
+(100℃〜250℃)程度に加熱して成形するもの
を言う。 例えば、射出成形、押出成形、プレス成
形などである。 【0020】 【発明の効果】本発明の溶融成形用透明帯電防止性樹脂
組成物は、押出成形や射出成形等の高温加工成形を行っ
ても樹脂本来の透明性を失わないで帯電防止性を付与す
ることができる。該樹脂組成物は、展示品表装用の樹脂
板、ショーケースのグレージング、自動車等のメーター
パネル、フレネルレンズ、レンチキュラーレンズ、光デ
ィスク、照明カバー、看板、透過型ディスプレイの前面
板などの各種成形品さらに各種フィルムに好適に利用で
きる。 【0021】 【実施例】以下実施例によって本発明をさらに詳しく説
明するが、本発明はこれら実施例によって制限されるも
のではない。なお、評価方法は以下のとおりである。 ・全光線透過率(Tt)及びヘイズ;ASTM D 1003-61に
準拠してポイック積分球式ヘイズメーター(日本精密光
学製SEP-HS-30D)により測定した。 ・帯電防止性:アクリル樹脂板を23℃、50%湿度の
状態に24時間放置した後、同雰囲気中でスタティック
オネストメータ(宍戸商会製)を用いて、印加電圧10
Kv、印加時間1分、テーブル回転数1300rpm、
の条件で帯電圧の半減期を測定した。 ・着色度;JIS-K7103に準拠し日本電色工業社製SZ−
Σ80分光式色差系を用い、黄色度(YI)を測定し
た。 ・吸水能:吸水性樹脂1gを純水で満たしたビーカーに
入れ、1時間攪拌した後、200メッシュの金網でろ過
した後、計量し増加した重量(g)を吸水量として算出
した。なお、全量該金網を通過する物質の場合は測定不
能とした。 【0022】実施例1,2、比較例1 メタアクリル樹脂ビーズ(スミペックスーEXA、住友
化学工業(株)製)表1に示す100重量部と、ウレタ
ン結合を有するポリエチレンオキサイド系吸水性樹脂
(吸水能30g水/g樹脂)を表1に示す量と酸化防止
剤(イルガノックス1010チバガイギー製)1重量部と
を、ヘンシェルミキサーで混合した後、押出機(一軸、
スクリュー径40mm、田辺プラスチック(株)製)で樹
脂温度265℃で混錬しペレット化した。得られたペレ
ットを射出成形機(名機製作所(株)製M-140SJ)によ
り成形温度260℃金型温度55℃で成形し、3mm厚の
平板成形品を得た。得られたシートの評価結果を表2に
示す。 【0023】実施例3、比較例2 実施例1と同じメタアクリル樹脂ビーズ100重量部
と、吸水性樹脂表1に示す量及び酸化防止剤とを、ヘン
シェルミキサーで混合した後、実施例1で使用した押出
機を用い、溶融樹脂を押出し、Tダイ、ポリシングロー
ル3本を介し、2mm厚、巾20cmのシートを得た。得ら
れたシートの評価結果を表2に示す。 【0024】比較例3,4 実施例1と同じメタアクリル樹脂ビーズ100重量部に
テトラエチレングリコールラウリルエーテルまたは、ポ
リプロピレンオキサイド/ポリエチレンオキサイド=2
/1のブロック共重合体を表1に示す量用い、実施例3
と同様にして、シートを得た、得られたシートの評価結
果を表2に示す。 【0025】比較例5 実施例1と同じメタアクリル樹脂ビーズと吸水性樹脂と
さらに過塩素酸リチウムを表1に示す量を用い、実施例
3と同様に行ってシートを得た。得られたシートの評価
結果を表2に示す。 【0026】 【表1】 【0027】 【表2】
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a transparent thermoplastic resin composition for melt molding which is excellent in heat resistance stability and antistatic property. Methacrylic resins, styrene resins and polycarbonates are known for their excellent transparency and beautiful appearance, and are used for signboards and various ornaments. However, these resins have problems in that they are easily charged with static electricity, have a reduced gloss, are easily soiled by dust and the like, and have a poor appearance. To solve this problem, many techniques have been proposed in which an alkyl sulfonate, a higher fatty acid monoglyceride, or a polyether ester amide is mixed in a methacrylic resin. For example, JP-A-3-122165 discloses a conductive resin containing 0.01% by weight or more and 20% by weight of an alkali metal salt and 0.5% by weight or more and 60% or less by weight of a polyether polymer in a transparent resin. Compositions are disclosed. In Japanese Patent Publication No. 4-98,
30 to 10% by weight of alkylaryl sulfonic acid lithium salt in a transparent polymer material, nonionic surfactant 70 to 9
It is described that 0.5 to 10% by weight of an antistatic agent consisting of 0% by weight is added and melt-kneaded to obtain a transparent polymer material. When the composition described in Japanese Patent Laid-Open No. 3-122165 is melt-molded, the polyether polymer contained therein is decomposed to cause coloration or antistatic property. Performance is often degraded. The composition described in Japanese Patent Publication No. 4-98 uses an agent having a relatively low molecular weight. Therefore, when the composition is melted and molded, it is vaporized and reduced, and the antistatic performance is deteriorated. Therefore, the present invention provides a resin composition excellent in transparency and antistatic property even when the resin composition is subjected to melt molding such as injection molding or extrusion molding. The present invention provides a transparent antistatic resin composition for melt molding which comprises 100 parts by weight of a transparent thermoplastic resin and 0.1 to 10 parts by weight of a water absorbent resin having a urethane bond. It is to provide things. The transparent thermoplastic resin used in the present invention includes, for example, polyethylene, polypropylene, ethylene-
Polyolefin resins such as vinyl acetate copolymers and ethylene-methyl methacrylate copolymers; acrylic resins whose main component is polymethylmethacrylate; styrene resins;
Vinyl chloride resin; polyester resin; polyacetal resin; polyamide resin; polycarbonate; polyimide resin and the like. These synthetic resins may be used alone or as a mixture and have high transparency. Above all,
Acrylic resin, styrene resin,
Polycarbonate or the like is preferable. More preferably, it is an acrylic resin. The acrylic resin contains methyl methacrylate alone or 50% by weight or more of methyl methacrylate and is copolymerizable with methyl methacrylate, for example, ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, Methacrylic acid esters such as phenyl methacrylate, benzyl methacrylate, 2-ethylhexyl methacrylate, 2-hydroxyethyl methacrylate, methyl acrylate, ethyl acrylate, butyl acrylate, cyclohexyl acrylate, phenyl acrylate, acrylic acid Acrylic esters such as benzyl, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate, etc., unsaturated fatty acids such as methacrylic acid, acrylic acid, styrene, α-methylstyrene, acrylonitrile, methyl ester Acrylonitrile, maleic acid anhydride,
It is a copolymer with phenylmaleimide, cyclohexylmaleimide, etc., but is not limited thereto. Further, it may further contain an elastomer component such as polybutadiene or polybutyl acrylate copolymer, a glutaric anhydride unit, or a glutarimide unit. The water-absorbent resin having a urethane bond in the present invention is obtained by reacting a polyether polyol with a compound having an isocyanate group. Polyether polyols include polyethylene glycol, polypropylene glycol polytetramethylene glycol, etc., and have one ether bond in the molecule.
No more than 00. Among the polyether polyols, polyethylene glycol is more excellent in water absorption capacity. In addition to the polyether polyol, other polyols are combined in an amount of less than 30% of the total polyol,
Alternatively, they can be co-condensed before use. As this polyol, polytetramethylene carbonate diol,
There are polycarbonate polyols such as polyhexamethylene carbonate diol; polyester polyols such as polycaprolactone diol. As the compound having an isocyanate group, a compound having two or more isocyanate groups in the molecule can be used. Examples include tetramethylene diisocyanate, hexamethylene diisocyanate, octamethylene diisocyanate, tolylene diisocyanate, 4,4-diphenylmethane diisocyanate, xylylene diisocyanate, lysine diisocyanate,
4,4-methylenebis (cyclohexyl isocyanate), methylcyclohexane-2,4 (2,6) -diisocyanate, isophorone diisocyanate, 1.3
-Or 1.4-bis (isocyanatomethyl) cyclohexane, trimethylhexamethylene diisocyanate, sulfonyl diisocyanate, and the like, and isocyanurate compounds obtained from the above-mentioned isocyanate compounds are also applicable. The molar ratio of the polyether polyol and the compound having an isocyanate group may be adjusted according to the target water absorption capacity. Specifically, polyether polyol / compound having isocyanate group = 70/30 to 50
/ 50 molar ratio, preferably 60/40 to 50/50
Thus, the higher the proportion of polyether polyol, the higher the water absorption capacity. The water absorption capacity of the water absorbent resin is 10 to 100 g water /
g resin. If it is less than 10 g water / g resin, the antistatic performance is difficult to be exhibited, and if it exceeds 100 g water / g resin, the resin may be deteriorated after being left for a long time. The amount of the water-absorbent resin is the amount of the transparent thermoplastic resin 1
It is 0.1 to 10 parts by weight per 00 parts by weight. Above all, 0.
5 to 5 parts by weight is preferable. If the amount added is less than 0.1 parts by weight, sufficient antistatic properties will not be exhibited, and if it is more than 10 parts by weight, not only the heat resistance will decrease, but also it will become difficult to be compatible with the transparent thermoplastic resin and the composition will become cloudy. I have something to do. The amount of the water-absorbent resin is more preferably depending on its water-absorbing capacity, more preferably, the value of g water / g resin of the water-absorbing capacity and the value of parts by weight of the water-absorbing resin per 100 parts by weight of the transparent thermoplastic resin. The product is 1 to 200. For the resin composition of the present invention, light diffusing agents, matting agents, dyes, pigments, light stabilizers, ultraviolet absorbers, antioxidants, reinforcing agents, fillers, mold release agents, flame retardants, etc. are well known. Additives may be added. If desired, an organic compound type antistatic agent may be used in combination. Known organic compound antistatic agents that can be used in combination include known alkyl sulfonates and higher fatty acid glycerides. However, an inorganic salt such as an inorganic perchlorate salt causes thermal decomposition of the water-absorbent resin, and therefore it should be avoided in combination. As the method for preparing the thermoplastic resin composition of the present invention from the transparent thermoplastic resin and the water absorbent resin having a urethane bond, both are mechanically mixed with a Henschel mixer, a tumbler, etc., and a Banbury mixer or a uniaxial mixer is used. There is a well-known method of melt-kneading with a twin screw extruder. The melt molding referred to in the present invention means molding by heating the thermoplastic resin to a temperature not lower than the melting point of the resin or to a glass transition temperature + (100 ° C. to 250 ° C.). For example, injection molding, extrusion molding, press molding and the like. INDUSTRIAL APPLICABILITY The transparent antistatic resin composition for melt molding of the present invention has an antistatic property without losing the transparency inherent to the resin even when it is subjected to high temperature processing molding such as extrusion molding or injection molding. Can be granted. The resin composition is used for various molded products such as resin plates for display of display products, glazing for showcases, meter panels for automobiles, Fresnel lenses, lenticular lenses, optical disks, lighting covers, signboards, front plates of transmissive displays, etc. It can be suitably used for various films. The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. The evaluation method is as follows. -Total light transmittance (Tt) and haze: Measured by a Poic integrating sphere type haze meter (SEP-HS-30D manufactured by Nippon Seimitsu Optical Co., Ltd.) according to ASTM D 1003-61. -Antistatic property: The acrylic resin plate was left at 23 ° C and 50% humidity for 24 hours, and then applied voltage 10 with a static Honest meter (manufactured by Shishido Shokai) in the same atmosphere.
Kv, application time 1 minute, table rotation speed 1300 rpm,
The half-life of the charged voltage was measured under the conditions.・ Coloring degree: SZ- manufactured by Nippon Denshoku Industries Co., Ltd. according to JIS-K7103
Yellowness (YI) was measured using a Σ80 spectral color difference system. Water absorption capacity: 1 g of the water-absorbent resin was placed in a beaker filled with pure water, stirred for 1 hour, filtered through a 200-mesh wire net, and then weighed and increased (g) was calculated as the amount of water absorption. In addition, when the whole amount of the substance passed through the wire net, the measurement was impossible. Examples 1 and 2, Comparative Example 1 Methacrylic resin beads (SUMIPEX-EXA, manufactured by Sumitomo Chemical Co., Ltd.) 100 parts by weight shown in Table 1 and a polyethylene oxide-based water-absorbing resin having a urethane bond (water-absorbing ability). An amount (30 g water / g resin) shown in Table 1 and 1 part by weight of an antioxidant (manufactured by Irganox 1010 Ciba Geigy) were mixed in a Henschel mixer, and then an extruder (uniaxial,
A screw having a diameter of 40 mm and manufactured by Tanabe Plastic Co., Ltd. was kneaded at a resin temperature of 265 ° C. and pelletized. The obtained pellets were molded with an injection molding machine (M-140SJ manufactured by Meiki Seisakusho Co., Ltd.) at a molding temperature of 260 ° C. and a mold temperature of 55 ° C. to obtain a flat plate molded product having a thickness of 3 mm. The evaluation results of the obtained sheet are shown in Table 2. Example 3, Comparative Example 2 100 parts by weight of the same methacrylic resin beads as in Example 1, the water-absorbent resin and the amounts and antioxidants shown in Table 1 were mixed in a Henschel mixer, and then in Example 1. The molten resin was extruded using the extruder used, and a sheet having a thickness of 2 mm and a width of 20 cm was obtained through a T-die and three polishing rolls. The evaluation results of the obtained sheet are shown in Table 2. Comparative Examples 3 and 4 100 parts by weight of the same methacrylic resin beads as in Example 1 were added to tetraethylene glycol lauryl ether or polypropylene oxide / polyethylene oxide = 2.
Example 3 using the block copolymer of 1/1 in the amount shown in Table 1.
A sheet was obtained in the same manner as above, and the evaluation results of the obtained sheet are shown in Table 2. Comparative Example 5 A sheet was obtained in the same manner as in Example 3, except that the same methacrylic resin beads, water absorbent resin and lithium perchlorate as in Example 1 were used in the amounts shown in Table 1. The evaluation results of the obtained sheet are shown in Table 2. [Table 1] [Table 2]

Claims (1)

【特許請求の範囲】 【請求項1】透明熱可塑性樹脂100重量部とウレタン
結合を有する吸水性樹脂0.1〜10重量部とからなる
溶融成形用透明帯電防止性樹脂組成物。 【請求項2】ウレタン結合を有する吸水性樹脂の吸水能
が10〜100g水/g樹脂であることを特徴とする
〔請求項1〕記載の溶融成形用透明帯電防止性樹脂組成
物。
Claim: What is claimed is: 1. A transparent antistatic resin composition for melt molding, which comprises 100 parts by weight of a transparent thermoplastic resin and 0.1 to 10 parts by weight of a water absorbent resin having a urethane bond. 2. The transparent antistatic resin composition for melt molding according to claim 1, wherein the water absorbing resin having a urethane bond has a water absorbing capacity of 10 to 100 g water / g resin.
JP31549993A 1993-12-15 1993-12-15 Transparent antistatic resin composition for melt molding Expired - Fee Related JP3304573B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31549993A JP3304573B2 (en) 1993-12-15 1993-12-15 Transparent antistatic resin composition for melt molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31549993A JP3304573B2 (en) 1993-12-15 1993-12-15 Transparent antistatic resin composition for melt molding

Publications (2)

Publication Number Publication Date
JPH07166074A true JPH07166074A (en) 1995-06-27
JP3304573B2 JP3304573B2 (en) 2002-07-22

Family

ID=18066104

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31549993A Expired - Fee Related JP3304573B2 (en) 1993-12-15 1993-12-15 Transparent antistatic resin composition for melt molding

Country Status (1)

Country Link
JP (1) JP3304573B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005055793A1 (en) * 2005-11-21 2007-05-24 Röhm Gmbh Transparent TPU (thermoplastic polyurethanes) / PMMA (polymethyl (meth) acrylate) Blends with improved impact resistance

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102005055793A1 (en) * 2005-11-21 2007-05-24 Röhm Gmbh Transparent TPU (thermoplastic polyurethanes) / PMMA (polymethyl (meth) acrylate) Blends with improved impact resistance

Also Published As

Publication number Publication date
JP3304573B2 (en) 2002-07-22

Similar Documents

Publication Publication Date Title
JP4439776B2 (en) Plastic optical parts
JPH073104A (en) Composition containing fluorinated-bisphenol-a-derived polycarbonate and polymethyl methacrylate
US5449709A (en) Resin composition for lens based materials
JPH07166074A (en) Transparent antistatic resin composition for melt molding
JPH09281307A (en) Screen for projection-type television set
JP2007153932A (en) Polycarbonate resin composition and its molding
JPH1017705A (en) Antistatic resin composition and its molded product
JP3284714B2 (en) Polyester film
JPH0812843A (en) Antistatic methacrylic resin composition
JP3391559B2 (en) Antistatic methacrylic resin composition
JP3371992B2 (en) Polycarbonate coextrusion product and its coextrusion method
JPH07207099A (en) Antistatic methacrylic resin composition
JPH1129685A (en) Antistatic acrylic resin composition
JPH10287740A (en) Polyether ester polycondensate
JPH1087944A (en) Antistatic methacrylic resin composition and its molding product
JPH0987458A (en) Antistatic methacrylic resin composition
JP3264058B2 (en) Antistatic methacrylic resin molding
JPH0912819A (en) Antistatic methacrylic resin composition
JPH10251389A (en) Polyether-ester polycondensate
JPH09279010A (en) Polycarbonate resin composition and molded product thereof
JPH09279009A (en) Polycarbonate resin composition and molded product thereof
JP2771675B2 (en) Polycarbonate laminate and method for producing the same
JPH1129630A (en) Polyetherester polycondensate
JP3047298B2 (en) Thermoplastic polymer composition
JPH08302146A (en) Antistatic methacrylic resin composition

Legal Events

Date Code Title Description
S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080510

Year of fee payment: 6

RD05 Notification of revocation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: R3D05

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090510

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100510

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100510

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110510

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110510

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120510

Year of fee payment: 10

LAPS Cancellation because of no payment of annual fees