JP3067254B2 - Thermoplastic resin composition - Google Patents

Thermoplastic resin composition

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Publication number
JP3067254B2
JP3067254B2 JP9900191A JP9900191A JP3067254B2 JP 3067254 B2 JP3067254 B2 JP 3067254B2 JP 9900191 A JP9900191 A JP 9900191A JP 9900191 A JP9900191 A JP 9900191A JP 3067254 B2 JP3067254 B2 JP 3067254B2
Authority
JP
Japan
Prior art keywords
thermoplastic resin
weight
ethylene
resin composition
parts
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.)
Expired - Fee Related
Application number
JP9900191A
Other languages
Japanese (ja)
Other versions
JPH04328167A (en
Inventor
久雄 田中
寿三男 原
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 JP9900191A priority Critical patent/JP3067254B2/en
Priority to CA002061644A priority patent/CA2061644A1/en
Priority to EP92103346A priority patent/EP0502420B1/en
Priority to DE69204086T priority patent/DE69204086T2/en
Priority to US07/846,126 priority patent/US5214091A/en
Publication of JPH04328167A publication Critical patent/JPH04328167A/en
Application granted granted Critical
Publication of JP3067254B2 publication Critical patent/JP3067254B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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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、熱可塑性樹脂組成物に
関するものである。さらに詳しくは、熱可塑性樹脂に、
非導電性無機充填剤およびエチレン−飽和カルボン酸ビ
ニルエステル共重合体けん化物のアルキレンオキサイド
付加物を含有してなる熱可塑性樹脂組成物に関するもの
である。本発明で得られる組成物は、フィルムやラミネ
ートなどの包装基材として、あるいは容器、コンテナの
ような成形製品として、さらには日用雑貨等としてのシ
ート、容器などに最適に使用され得るものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermoplastic resin composition. More specifically, for thermoplastic resin,
The present invention relates to a thermoplastic resin composition containing a non-conductive inorganic filler and an alkylene oxide adduct of a saponified ethylene-saturated carboxylic acid vinyl ester copolymer. The composition obtained in the present invention can be optimally used as a packaging base material such as a film or a laminate, or as a molded product such as a container or a container, and further as a sheet or a container as daily necessities. is there.

【0002】[0002]

【従来の技術】熱可塑性樹脂への無機充填剤の添加は、
樹脂の機械的な性質の改良、省プラスチックによるコス
ト低下や環境対策、あるいは廃プラスチックの焼却時の
燃焼カロリー低減による焼却設備の負荷低減などの目的
によく行なわれており、例えばポリエチレンやポリプロ
ピレンのようなポリオレフィンに炭酸カルシウムやタル
クを混合し、シート化、成形などによりフィルムや成形
品として実用に供されている。
2. Description of the Related Art The addition of inorganic fillers to thermoplastic resins
Often used for the purpose of improving the mechanical properties of resins, reducing costs and environmental measures by saving plastics, and reducing the load on incineration facilities by reducing the calories burned when incinerating waste plastics, such as polyethylene and polypropylene. It is practically used as a film or molded product by mixing calcium carbonate or talc with a suitable polyolefin, forming a sheet, or molding.

【0003】しかし熱可塑性樹脂に無機充填剤を添加し
ても、機械的な混合であって化学変化が伴わないだけ
に、無機充填剤の分散不良により、均一なフィルムや成
形品が得難く、機械的な性質が低下する問題がある。
[0003] However, even if an inorganic filler is added to a thermoplastic resin, it is difficult to obtain a uniform film or molded article due to poor dispersion of the inorganic filler because of mechanical mixing and no chemical change. There is a problem that the mechanical properties deteriorate.

【0004】たとえば無機充填剤を多量に添加した場合
には、樹脂の柔軟性をそこなったり、強度が低下するな
ど物性的に悪影響を受ける問題がある。また場合によっ
ては無機充填剤が樹脂の表面に粉状に浮きだして、汚染
性のフィルムや成形物となることもある。
[0004] For example, when a large amount of an inorganic filler is added, there is a problem that physical properties are adversely affected, such as losing flexibility of the resin and decreasing strength. Further, in some cases, the inorganic filler may float out in a powder form on the surface of the resin, resulting in a contaminating film or molded product.

【0005】そこでバインダーとしての添加剤を配合す
ることが考えられるが、ポリオレフィン樹脂との相溶性
が低い添加剤は、添加剤自身が樹脂表面に移行して、粘
着性や汚染性を示す問題があり得る。
Therefore, it is conceivable to add an additive as a binder. However, an additive having low compatibility with the polyolefin resin has a problem that the additive itself migrates to the resin surface and shows tackiness and stain. possible.

【0006】その改良のため、例えばエチレンオキサイ
ド系および/またはプロピレンオキサイド系の液状ポリ
マーを添加してなるポリオレフィン樹脂組成物が提案さ
れているが(特開昭55−165934号公報)、該液
状ポリマーも樹脂との相溶性があまりよくなく、時間と
ともに表面にポリマーが移行しベタツキを起こす傾向が
ある。
For the purpose of improvement, there has been proposed a polyolefin resin composition to which, for example, an ethylene oxide-based and / or propylene oxide-based liquid polymer has been added (JP-A-55-165934). However, the compatibility with the resin is not so good, and the polymer tends to migrate to the surface with time and cause stickiness.

【0007】[0007]

【発明が解決しようとする課題】本発明は、非導電性無
機充填剤の添加の際に、本来の樹脂の物性を維持しなが
ら、樹脂との相溶性にすぐれ、しかも非導電性無機充填
剤の分散性をよくする添加剤を検討するなかから到達し
た、熱可塑性樹脂組成物に関するものである。
SUMMARY OF THE INVENTION The present invention relates to a non-conductive inorganic filler which is excellent in compatibility with a resin while maintaining the original properties of the resin when the non-conductive inorganic filler is added. The present invention relates to a thermoplastic resin composition which has been reached from the study of an additive for improving the dispersibility of a thermoplastic resin.

【0008】[0008]

【課題を解決するための手段】すなわち本発明は、熱可
塑性樹脂たとえばポリエチレン、ポリプロピレン30〜
95重量部、非導電性無機充填剤たとえば炭酸カルシウ
ムやタルクを5〜70重量部およびエチレン−飽和カル
ボン酸ビニルエステル(たとえば酢酸ビニル)共重合体
けん化物のアルキレンオキサイド(たとえばエチレンオ
キサイド)付加物0.1〜10重量部を含有することを
特徴とする熱可塑性樹脂組成物に関するものである。
That is, the present invention relates to a thermoplastic resin such as polyethylene or polypropylene.
95 parts by weight, 5 to 70 parts by weight of a non-conductive inorganic filler such as calcium carbonate or talc, and an alkylene oxide (eg, ethylene oxide) adduct of a saponified ethylene-saturated carboxylic acid vinyl ester (eg, vinyl acetate) copolymer 0 The present invention relates to a thermoplastic resin composition containing from 1 to 10 parts by weight.

【0009】本発明に用いられる熱可塑性樹脂として
は、ポリオレフィンたとえばポリエチレン、ポリプロピ
レン、エチレン−プロピレン共重合体樹脂、エチレン−
ブテン−1共重合体樹脂、ポリメチルペンテンなどのオ
レフィンモノマーの重合体、共重合体およびその混合物
が、またビニル結合含有モノマーの重合体たとえばポリ
スチレン、ポリ塩化ビニル、ポリ塩化ビニリデン、エチ
レン−酢酸ビニル共重合体、スチレン−アクリロニトリ
ル共重合体などが、さらにはジエン結合含有モノマーと
の共重合体たとえばスチレン−ブタジエン−アクリロニ
トリル共重合体などが例示される。
As the thermoplastic resin used in the present invention, polyolefins such as polyethylene, polypropylene, ethylene-propylene copolymer resin, ethylene-
Polymers of olefin monomers such as butene-1 copolymer resin and polymethylpentene, copolymers and mixtures thereof, and polymers of vinyl bond-containing monomers such as polystyrene, polyvinyl chloride, polyvinylidene chloride, ethylene-vinyl acetate Examples thereof include copolymers, styrene-acrylonitrile copolymers, and copolymers with a diene bond-containing monomer, such as styrene-butadiene-acrylonitrile copolymer.

【0010】本発明に用いられる非導電性無機充填剤と
しては、炭酸カルシウム、タルク、クレー、シリカ、硫
酸バリウム、マイカ、ガラス粉などに代表される非導電
性無機化合物があり、それぞれの単独もしくは併用使用
が可能である。
As the non-conductive inorganic filler used in the present invention, there are non-conductive inorganic compounds represented by calcium carbonate, talc, clay, silica, barium sulfate, mica, glass powder and the like. It can be used in combination.

【0011】非導電性無機充填剤の添加量としては熱可
塑性樹脂30〜95重量部に対して5〜70重量部が適
当である。5重量部よりも少ないと添加の目的に対して
実用的ではなく、70重量部よりも多いと、熱可塑性樹
脂の特性を大きく損なって、フィルムや成形品としての
実用性に乏しくなってしまうので好ましくない。
An appropriate amount of the non-conductive inorganic filler is 5 to 70 parts by weight based on 30 to 95 parts by weight of the thermoplastic resin. If it is less than 5 parts by weight, it is not practical for the purpose of addition, and if it is more than 70 parts by weight, the properties of the thermoplastic resin are greatly impaired, and the practicality as a film or molded article becomes poor. Not preferred.

【0012】本発明に用いられるエチレン−飽和カルボ
ン酸ビニルエステル共重合体けん化物のアルキレンオキ
サイド付加物において、エチレン−飽和カルボン酸ビニ
ルエステル共重合体は公知の方法たとえば高圧ラジカル
重合で製造できる。
In the alkylene oxide adduct of the saponified ethylene-saturated carboxylic acid vinyl ester copolymer used in the present invention, the ethylene-saturated carboxylic acid vinyl ester copolymer can be produced by a known method, for example, high-pressure radical polymerization.

【0013】飽和カルボン酸ビニルエステルとしては特
に制限されることなく、広範なものが使用できるが、そ
の具体例としては酢酸ビニル、プロピオン酸ビニル、酪
酸ビニルなどが示され、特に酢酸ビニルが好ましい。
The saturated vinyl carboxylate is not particularly limited, and a wide range can be used. Specific examples thereof include vinyl acetate, vinyl propionate and vinyl butyrate, with vinyl acetate being particularly preferred.

【0014】またエチレンと飽和カルボン酸ビニルエス
テルとを共重合するに際して、少量の不飽和カルボン酸
のアルキルエステル、例えばアクリル酸メチル、メタク
リル酸メチルなどを共存させて多元共重合体としたもの
も含まれる。
When ethylene and a saturated vinyl carboxylate are copolymerized, a copolymer obtained by coexisting a small amount of an alkyl ester of an unsaturated carboxylic acid, such as methyl acrylate or methyl methacrylate, is also included. It is.

【0015】エチレン−飽和カルボン酸ビニルエステル
共重合体のエチレン含有量および数平均分子量について
特に制限はないが、各々1〜90重量%および1,00
0〜20,000の範囲が特に好ましい。
The ethylene content and the number average molecular weight of the ethylene-saturated carboxylic acid vinyl ester copolymer are not particularly limited, but are 1 to 90% by weight and 1,000
The range of 0 to 20,000 is particularly preferred.

【0016】本発明に用いられるエチレン−飽和カルボ
ン酸ビニルエステル共重合体けん化物のアルキレンオキ
サイド付加物(以下、単に「付加物」と記すことがあ
る)とは、エチレン−飽和カルボン酸ビニルエステル共
重合体けん化物に対して、アルキレンオキサイドを付加
して得られるものである。
The alkylene oxide adduct (hereinafter sometimes simply referred to as "adduct") of the saponified ethylene-saturated carboxylic acid vinyl ester copolymer used in the present invention refers to an ethylene-saturated carboxylic acid vinyl ester copolymer. It is obtained by adding an alkylene oxide to a saponified polymer.

【0017】アルキレンオキサイドとしては、特に制限
されることなく広範なものが使用され得るが、例えばそ
の具体例をあげるならば、エチレンオキサイド、プロピ
レンオキサイド、ブチレンオキサイド等が例示される
が、これらの1種もしくは2種以上をブロックまたはラ
ンダムに付加したものでもよく、なかでもエチレンオキ
サイドが特に好ましい。
As the alkylene oxide, a wide range can be used without any particular limitation. For example, ethylene oxide, propylene oxide, butylene oxide and the like can be mentioned as specific examples. Species or two or more species may be added in a block or random manner, and among them, ethylene oxide is particularly preferred.

【0018】エチレン−飽和カルボン酸ビニルエステル
共重合体けん化物の、けん化率についても特に制限はな
いが、30〜100%の範囲が好ましく、50〜100
%の範囲が特に好ましい。
The saponification rate of the saponified ethylene-saturated carboxylic acid vinyl ester copolymer is not particularly limited, but is preferably in the range of 30 to 100%, more preferably 50 to 100%.
% Is particularly preferred.

【0019】エチレン−飽和カルボン酸ビニルエステル
共重合体けん化物に対するアルキレンオキサイドの付加
量についても特に制限はないが、該けん化物100重量
部に対して20〜1000重量部の範囲が好ましい。
The amount of the alkylene oxide added to the saponified ethylene-saturated carboxylic acid vinyl ester copolymer is not particularly limited, but is preferably in the range of 20 to 1,000 parts by weight based on 100 parts by weight of the saponified product.

【0020】本発明に用いられる付加物の製法に特に制
限はないが、例えば次の様にして得られる。まず、エチ
レン−飽和カルボン酸ビニルエステル共重合体を、アル
コール中でアルカリの存在下で加熱することにより、エ
チレン−飽和カルボン酸ビニルエステル共重合体けん化
物を得る。つぎに該けん化物とアルキレンオキサイドを
アルカリの存在下に加熱、反応させる。かくして得られ
る反応物より、本発明の付加物が取得される。
Although there is no particular limitation on the method for producing the adduct used in the present invention, it can be obtained, for example, as follows. First, a saponified ethylene-saturated carboxylic acid vinyl ester copolymer is obtained by heating the ethylene-saturated carboxylic acid vinyl ester copolymer in an alcohol in the presence of an alkali. Next, the saponified product and the alkylene oxide are heated and reacted in the presence of an alkali. From the reactants thus obtained, the adduct of the present invention is obtained.

【0021】付加物の添加量は、熱可塑性樹脂30〜7
0重量部に対して0.1〜10重量部の範囲が好まし
い。付加物の添加量が0.1重量部よりも少ないと、非
導電性無機充填剤の分散効果がわずかであり、実用的に
不適である。また10重量部よりも多いと、熱可塑性樹
脂のもつ強度等の特性を低下させるので実用的に不適で
ある。
The addition amount of the additive is 30 to 7 for the thermoplastic resin.
The range is preferably 0.1 to 10 parts by weight with respect to 0 parts by weight. If the amount of the additive is less than 0.1 part by weight, the effect of dispersing the non-conductive inorganic filler is slight, which is not suitable for practical use. On the other hand, if the amount is more than 10 parts by weight, the properties such as strength of the thermoplastic resin are reduced, which is not suitable for practical use.

【0022】本発明において、熱可塑性樹脂に、非導電
性無機充填剤および付加物を添加してなる熱可塑性樹脂
組成物を得る方法に特に制限はないが、熱可塑性樹脂の
溶融温度において、熱可塑性樹脂、非導電性無機充填
剤、付加物それぞれを個別に添加する方法、あるいはま
ず2種類の物質をあらかじめ混合しておき、残る物質を
続いて添加混合する方法などが用いられ、混合機械とし
ては、バンバリーミキサー、オープンロール、ニーダ
ー、ヘンシェルミキサー等の一般的な混合機械、手段か
ら選択できる。
In the present invention, there is no particular limitation on a method for obtaining a thermoplastic resin composition obtained by adding a non-conductive inorganic filler and an additive to a thermoplastic resin. A method of individually adding a plastic resin, a non-conductive inorganic filler, and an additive, or a method of mixing two types of substances in advance and then adding and mixing the remaining substances is used as a mixing machine. Can be selected from general mixing machines and means such as a Banbury mixer, an open roll, a kneader, and a Henschel mixer.

【0023】本発明の熱可塑性樹脂組成物には、一般的
に熱可塑性樹脂に添加される、熱安定剤、酸化防止剤、
光安定剤、滑剤、帯電防止剤、防曇剤、顔料、発泡剤、
蛍光剤、難燃剤、離型剤、加工助剤、補強剤などを必要
に応じて包含してもよい。
The thermoplastic resin composition of the present invention generally comprises a heat stabilizer, an antioxidant,
Light stabilizers, lubricants, antistatic agents, antifogging agents, pigments, foaming agents,
Fluorescent agents, flame retardants, release agents, processing aids, reinforcing agents, and the like may be included as necessary.

【0024】[0024]

【実施例】以下に実施例および比較例によって本発明の
効果を具体的に説明するが、本発明はこれらによって限
定されるものではない。
EXAMPLES The effects of the present invention will be specifically described below with reference to examples and comparative examples, but the present invention is not limited to these examples.

【0025】実施例−1、2 低密度ポリエチレンと炭酸カルシウムと、エチレン含有
量31重量%、数平均分子量1900のエチレン−酢酸
ビニル共重合体の90%けん化物へのエチレンオキサイ
ド200%付加物(付加物−1)とを表1に示す量を、
バンバリーミキサーにて150℃で10分間混練した。
続いて厚さ1mmのシートをプレス成形機を用いて16
0℃で作成した。得られたシートの外観、引張物性を表
1にまとめて記す。
Examples 1, 2 Low-density polyethylene, calcium carbonate, 200% ethylene oxide adduct to 90% saponified ethylene-vinyl acetate copolymer having an ethylene content of 31% by weight and a number average molecular weight of 1900 ( And the amount shown in Table 1 as
The mixture was kneaded with a Banbury mixer at 150 ° C. for 10 minutes.
Subsequently, a sheet having a thickness of 1 mm was formed using a press forming machine.
Prepared at 0 ° C. Table 1 summarizes the appearance and tensile properties of the obtained sheet.

【0026】実施例−3、4 エチレン含有量31重量%、数平均分子量1900のエ
チレン−酢酸ビニル共重合体の60%けん化物へのエチ
レンオキサイド200%付加物(付加物−2)を用いた
以外は、実施例−1と同様に混練し、続いてシート化し
物性を調べた。結果を表1にまとめて記す。
Examples 3, 4 A 200% ethylene oxide adduct (adduct-2) was used to a 60% saponified ethylene-vinyl acetate copolymer having an ethylene content of 31% by weight and a number average molecular weight of 1900. Except for the above, kneading was carried out in the same manner as in Example 1, followed by sheeting and physical properties were examined. The results are summarized in Table 1.

【0027】実施例−5、6 エチレン含有量31重量%、数平均分子量1900のエ
チレン−酢酸ビニル共重合体の90%けん化物へのエチ
レンオキサイド500%付加物(付加物−3)を用いた
以外は、実施例−1と同様に混練し、続いてシート化し
物性を調べた。結果を表1にまとめて記す。
Examples -5 and 6 A 500% ethylene oxide adduct (adduct-3) was used to a 90% saponified ethylene-vinyl acetate copolymer having an ethylene content of 31% by weight and a number average molecular weight of 1900. Except for the above, kneading was carried out in the same manner as in Example 1, followed by sheeting and physical properties were examined. The results are summarized in Table 1.

【0028】実施例−7、8 エチレン含有量16重量%、数平均分子量2400のエ
チレン−酢酸ビニル共重合体の90%けん化物へのエチ
レンオキサイド200%付加物(付加物−4)を用いた
以外は、実施例−1と同様に混練し、続いてシート化し
物性を調べた。結果を表1にまとめて記す。
Examples -7 and 8 A 200% ethylene oxide adduct (adduct-4) was used to a 90% saponified ethylene-vinyl acetate copolymer having an ethylene content of 16% by weight and a number average molecular weight of 2400. Except for the above, kneading was carried out in the same manner as in Example 1, followed by sheeting and physical properties were examined. The results are summarized in Table 1.

【0029】比較例−1、5 低密度ポリエチレンと炭酸カルシウム、分子量600ま
たは4,000のポリエチレングリコールとを表2に示
す量を、実施例−1と同様に混練し、続いてシート化し
て物性を調べた。結果を表2にまとめて記す。
COMPARATIVE EXAMPLES-1, 5 Low-density polyethylene, calcium carbonate, and polyethylene glycol having a molecular weight of 600 or 4,000 were kneaded in the amounts shown in Table 2 in the same manner as in Example 1, and then kneaded to form a sheet. Was examined. The results are summarized in Table 2.

【0030】使用原料および評価方法は次の通り。 使用原料 樹脂 住友化学工業社製 低密度ポリエ
チレン(スミカセンL−705) 炭酸カルシウム 井上石灰工業社製 重質炭酸カル
シウム(ベスタBS) 付加物 実施例参照 評価方法(いずれもシート作成後、23℃、50%湿度
下で1週間保存してから評価) シートの表面状態 シート表面を観察して、炭酸カルシ
ウムの混合ムラや付加物あるいはポリエチレングリコー
ルの汚染性が無い場合を良好と判定した。 引張試験 JIS K6730(1981年)
に準拠して測定した。 表面固有抵抗率 東亜電波工業社製 超絶縁計SM−
10E型により測定した。(23℃×50%RH)
The raw materials used and the evaluation method are as follows. Raw materials used Resin Low-density polyethylene (Sumikacene L-705) manufactured by Sumitomo Chemical Co., Ltd. Calcium carbonate Heavy calcium carbonate (Vesta BS) manufactured by Inoue Lime Industry Co., Ltd. (Evaluated after storage under 1% humidity for one week) Surface condition of sheet The surface of the sheet was observed, and a case where there was no mixing unevenness of calcium carbonate, no adducts, or contamination of polyethylene glycol was judged to be good. Tensile test JIS K6730 (1981)
It measured according to. Surface specific resistivity Toa Denpa Kogyo Co., Ltd. super insulation meter SM-
It was measured with a model 10E. (23 ° C x 50% RH)

【0031】 [0031]

【0032】 [0032]

【0033】[0033]

【発明の効果】以上述べた通り、本発明による熱可塑性
樹脂組成物は、シートの外観に優れ、引張伸び特性が改
良でき、従来の技術において問題であった、シートの外
観や引張伸び特性の低下などを改善するものであり、そ
の工業的な価値は極めて高いものである。
As described above, the thermoplastic resin composition according to the present invention has excellent sheet appearance and improved tensile elongation properties, and has a problem in sheet appearance and tensile elongation properties, which have been problems in the prior art. It is intended to improve reduction and the like, and its industrial value is extremely high.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI C08L 23:26) (C08L 101/00 29:04) (58)調査した分野(Int.Cl.7,DB名) C08L 1/00 - 101/16 C08K 3/00 - 13/08 ──────────────────────────────────────────────────続 き Continuation of the front page (51) Int.Cl. 7 identification code FI C08L 23:26) (C08L 101/00 29:04) (58) Investigated field (Int.Cl. 7 , DB name) C08L 1 / 00-101/16 C08K 3/00-13/08

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】熱可塑性樹脂30〜95重量部、非導電性
無機充填剤5〜70重量部およびエチレン−飽和カルボ
ン酸ビニルエステル共重合体けん化物のアルキレンオキ
サイド付加物0.1〜10重量部を含有することを特徴
とする熱可塑性樹脂組成物。
1. A thermoplastic resin (30 to 95 parts by weight), a nonconductive inorganic filler (5 to 70 parts by weight) and an alkylene oxide adduct of a saponified ethylene-saturated carboxylic acid vinyl ester copolymer (0.1 to 10 parts by weight). A thermoplastic resin composition comprising:
【請求項2】熱可塑性樹脂がポリエチレンおよび/また
はポリプロピレンであり、非導電性無機充填剤が炭酸カ
ルシウムまたはタルクである請求項1記載の熱可塑性樹
脂組成物。
2. The thermoplastic resin composition according to claim 1, wherein the thermoplastic resin is polyethylene and / or polypropylene, and the non-conductive inorganic filler is calcium carbonate or talc.
【請求項3】エチレン−飽和カルボン酸ビニルエステル
共重合体けん化物のアルキレンオキサイド付加物が、エ
チレン単位含有量1〜90重量%、数平均分子量1,0
00〜20,000のエチレン−飽和カルボン酸ビニル
エステル共重合体のけん化物であって、そのけん化率が
30〜100%であり、アルキレンオキサイド付加量
が、該けん化物100重量部に対して20〜1000重
量部である請求項1記載の熱可塑性樹脂組成物。
3. An alkylene oxide adduct of a saponified ethylene-saturated carboxylic acid vinyl ester copolymer having an ethylene unit content of 1 to 90% by weight and a number average molecular weight of 1,0.
A saponified ethylene-saturated carboxylic acid vinyl ester copolymer having a saponification ratio of 30 to 100% and an alkylene oxide addition amount of 20 to 100 parts by weight of the saponified product. The thermoplastic resin composition according to claim 1, wherein the amount is from 1000 to 1000 parts by weight.
【請求項4】飽和カルボン酸ビニルエステルが、酢酸ビ
ニルである請求項1記載の熱可塑性樹脂組成物。
4. The thermoplastic resin composition according to claim 1, wherein the saturated carboxylic acid vinyl ester is vinyl acetate.
【請求項5】アルキレンオキサイドがエチレンオキサイ
ドである請求項1記載の熱可塑性樹脂組成物。
5. The thermoplastic resin composition according to claim 1, wherein the alkylene oxide is ethylene oxide.
JP9900191A 1991-03-05 1991-04-30 Thermoplastic resin composition Expired - Fee Related JP3067254B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP9900191A JP3067254B2 (en) 1991-04-30 1991-04-30 Thermoplastic resin composition
CA002061644A CA2061644A1 (en) 1991-03-05 1992-02-21 Thermoplastic resin composition
EP92103346A EP0502420B1 (en) 1991-03-05 1992-02-27 Thermoplastic resin composition
DE69204086T DE69204086T2 (en) 1991-03-05 1992-02-27 Thermoplastic resin composition.
US07/846,126 US5214091A (en) 1991-03-05 1992-03-04 Thermoplastic resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9900191A JP3067254B2 (en) 1991-04-30 1991-04-30 Thermoplastic resin composition

Publications (2)

Publication Number Publication Date
JPH04328167A JPH04328167A (en) 1992-11-17
JP3067254B2 true JP3067254B2 (en) 2000-07-17

Family

ID=14234755

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9900191A Expired - Fee Related JP3067254B2 (en) 1991-03-05 1991-04-30 Thermoplastic resin composition

Country Status (1)

Country Link
JP (1) JP3067254B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3243851B2 (en) * 1992-09-03 2002-01-07 住友化学工業株式会社 Flowability improver for thermoplastic resin

Also Published As

Publication number Publication date
JPH04328167A (en) 1992-11-17

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