JPS6172061A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPS6172061A
JPS6172061A JP19616784A JP19616784A JPS6172061A JP S6172061 A JPS6172061 A JP S6172061A JP 19616784 A JP19616784 A JP 19616784A JP 19616784 A JP19616784 A JP 19616784A JP S6172061 A JPS6172061 A JP S6172061A
Authority
JP
Japan
Prior art keywords
resin
parts
alkali metal
resin composition
polar aprotic
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
JP19616784A
Other languages
Japanese (ja)
Inventor
Tetsuo Mitani
徹男 三谷
Katsuyoshi Iizaka
飯阪 捷義
Fumiaki Baba
文明 馬場
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 Electric Corp
Original Assignee
Mitsubishi Electric Corp
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 Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP19616784A priority Critical patent/JPS6172061A/en
Priority to DE3532805A priority patent/DE3532805C2/en
Priority to US06/776,885 priority patent/US4687801A/en
Publication of JPS6172061A publication Critical patent/JPS6172061A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a resin composition capable of keeping excellent antistatic property even in low-humidity environment, and resistant to the lowering of the antistatic property by washing, by adding specific amounts of an alkali metal salt and a polar aprotic solvent to a thermoplastic resin. CONSTITUTION:100 pts. (wt.) of a thermoplastic resin (e.g. acrylic resin, polycar bonate resin, etc.) is compounded with (A) 0.1-30pts. of an alkali metal salt (e.g. lithium perchlorate, potassium perchlorate, etc.) and (B) 1-30pts. of a polar aprotic solvent (e.g. propylene carbonate, ethylene carbonate, etc.)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発I:!I:Iは帯電防止効果金有する叫脂組成物
に関するものである。
[Detailed description of the invention] [Industrial application field] This invention I:! I:I relates to a glaucoma composition having an antistatic effect.

[従来の技術〕 一般Vこプラスチックげ電気抵抗が大きく、#最等によ
って容易に帯電しやすぐ、ゴミやホコリ金吸引して外観
を損ねたり、電気・電子1戊器の誤動作や故障などの原
因1/(なっている。
[Prior art] General V plastics have high electrical resistance and can easily become charged and attract dust and dirt, damaging the appearance and causing malfunctions and breakdowns in electrical and electronic devices. Cause 1/(has become.

このような帯電しやすいプラスチックの蛍戒性?低下さ
せるためには、蛍厄防止剤全塗布したり内部練り込みで
行なうことが知らhでいる。塗布用の帯電防止剤として
は通常界面活性剤やシリコン系化合物か用いられる。
Is this kind of plastic easily charged with electricity? It is known that in order to reduce this, it is possible to apply an anti-fluorescent agent to the entire surface or to mix it into the interior. As the antistatic agent for coating, a surfactant or a silicone compound is usually used.

〔発(7)が解決しようとつる問題点〕し刀為し界[…
活性剤は洗浄によって脱落しやすぐ長期間の帝シ防止効
呆は期待L!IlIい。シリコン系化合物げかなり良好
7x帯゛ル防止効果か期待でAるが、塗布条件の管理か
難しく、作業能高も悪く、コスト的に不利な面がある。
[The problem that Hatsu (7) is trying to solve] and the sword fighting world [...
The active agent falls off when washed and is expected to have long-term anti-seizure effect! IlI. Silicon-based compounds have a fairly good 7x band prevention effect and are expected to be A, but they are difficult to control coating conditions, have poor workability, and are disadvantageous in terms of cost.

帯電防止剤の内部裸り込み法は、帯電防止剤か表面にし
み出すことにより帝′醒防止効果に発埃するため、水洗
や摩寿により効果は激職し、帯電防止効果の回復VCは
長時1川を要する。
In the method of internally soaking the antistatic agent, the antistatic agent oozes out onto the surface and generates dust, so washing with water or washing it with water will greatly reduce the effect, and the recovery of the antistatic effect will be difficult. It takes a long time and one river.

1k、上記のいずれの方法とも、空気中の水分全表向に
吸着することにより、樹脂表面のイオン云導性を増大さ
せて帯電防止効果を発均させるーものである!こめ、水
の存在は不可欠であり、低湿朋の環境においては帯電防
止効果か小さくなる専の問題点か15つだ。
1k, all of the above methods increase the ionic conductivity of the resin surface by adsorbing the moisture in the air on the entire surface, and even out the antistatic effect! Therefore, the presence of water is essential, and in a low-humidity environment, the antistatic effect is reduced, which is a major problem.

この発明は上記した従来のものの問題点を商去するため
になさねたもので、低湿度の環視中においても良好な帯
電防止効果全保持し、洗浄によって帯電防止性が低ドし
ないW脂組成物を提供することを目的としている。
This invention was made in order to eliminate the above-mentioned problems of the conventional products, and it has a W resin composition that retains all good antistatic effects even during low-humidity monitoring, and that does not lose its antistatic properties when washed. The purpose is to provide something.

〔間捌点を解決するための手段〕[Means for resolving the gap]

この発明の樹脂組成物け、熱可塑性樹脂にアルカリ金属
塩と極性非プロトン溶媒を含ませたものである。
The resin composition of this invention is a thermoplastic resin containing an alkali metal salt and a polar aprotic solvent.

[作用〕 この発明の側脂f、11成物において、アルカリ金属塩
ぽ樹脂組成物中に溶解してイオン解離しており。
[Function] In the side fat f and 11 compositions of the present invention, they are dissolved in the alkali metal salt resin composition and ionically dissociated.

覗界が印加さhハば、このイオンが樹脂組成物中を移I
IL11シて厄荷を中和しようとすることにより帯電防
止効果を示す。極性非プロトン溶媒げ非水下に2いてイ
オン解離を促進する。この促進作用により帯電防止効果
は充分に発揮される。なお、熱可塑性樹脂としてアクリ
ル樹脂を用いねば、アルカリ金kJ4塩および車性非プ
ロトンM媒げアクリル系樹脂に対し良好な相溶性かあり
、分子分散またけそ稍に近い形で溶解しているため、ア
クリル系樹脂の反好な透明性を保持することかでたる。
When a viewing field is applied, these ions migrate through the resin composition.
IL11 shows an antistatic effect by trying to neutralize harmful loads. A polar aprotic solvent is used under water to promote ionic dissociation. Due to this accelerating action, the antistatic effect is fully exhibited. In addition, if an acrylic resin is used as the thermoplastic resin, it has good compatibility with the alkali gold KJ4 salt and the car-based aproton M-carrying acrylic resin, and is dissolved in a form close to molecular dispersion or sparse. The main reason for this is that it maintains the transparency that acrylic resin has.

〔夷箔例〕[Example of Eibaku]

熱可塑性樹脂に含プハるアルカリ金慎塩及び極性非プロ
トン溶媒の緘にげ適当な範囲がある。熱可塑性樹脂10
0皇竹部に対して、アルカリ8−属塩の配合割合は0.
1軍量部から30 JI量部の範囲が望ましい。アルカ
リ金属塩か0.1 i 識部未満でげ専電性の同上げ小
さく、帯電防止効果か少ない。
There is a suitable range of alkali metal salts and polar aprotic solvents contained in thermoplastic resins. Thermoplastic resin 10
The blending ratio of alkali 8-group salt to 0 Kotake part is 0.
A range of 1 military part to 30 JI parts is desirable. Alkali metal salts are less than 0.1 i, have a small electrical property, and have little antistatic effect.

また、アルカリ金属塩か3ON量部金越えると結晶が析
出しやすぐなり、樹脂組成物けもろぐなる。
Further, if the amount of the alkali metal salt exceeds 3ON, crystals will precipitate and the resin composition will become sluggish.

極性非プロトン溶媒の配合割合げ1軍事部から307I
r惜部が電せしい。極性非プロトン溶媒が1軍量部未調
ではイオン解離の促進効果は非常に少なく、30車景部
′に@オると樹脂組成物の熱変形温度か著しく低下し、
通常のプラスチック成形材料としての価値が少なくなる
Blending ratio of polar aprotic solvent 1 307I from the Ministry of Military Affairs
The regrettable part seems to be electric. If the amount of polar aprotic solvent is less than 1 part, the effect of promoting ion dissociation is very small, and if it exceeds 30 parts, the heat distortion temperature of the resin composition will drop significantly.
It has less value as a normal plastic molding material.

この発明に係わる熱可塑性樹脂としてけ熱斐形m呟が常
諷エリ蘭(、vJ7常の成形、例えば射出底形、押出成
形や圧縮成形の可能な樹脂を用いることがで致る。例え
ばアクリル系樹脂、ポリカーボネート側脂、アクリロニ
トリルーブタジエンースチレ/樹脂、アクリロニトリル
−スチレン樹脂。
As the thermoplastic resin according to this invention, resins that can be molded in a conventional manner, such as injection molding, extrusion molding, or compression molding, can be used. For example, acrylic resin. system resin, polycarbonate side fat, acrylonitrile-butadiene-styrene/resin, acrylonitrile-styrene resin.

スチレン樹脂、ポリアミド糸樹脂、ポリエステル系樹脂
等か用いI−1ねるが、アルカリ金属塩と極性非プロト
ン溶媒に相溶性の良い樹脂であhば、こf1以外の熱可
塑性樹脂か用いらねゐことげ言う寸でもない。
Styrene resin, polyamide thread resin, polyester resin, etc. can be used for I-1, but thermoplastic resins other than F1 can be used as long as the resin has good compatibility with alkali metal salts and polar aprotic solvents. It's not even worth mentioning.

この発明に係わるアルカリ金属塩げ公矧のものを1釉以
上用いることがで話る。例λば過塩諧酸リチウム、過塩
素酸カリウム、過塩素酸ナトリウム、a塩化リチウム、
チオシアン−9リチウム。
It is possible to use one or more glazes made of alkali metal salts according to the present invention. Examples: Lithium perchlorate, potassium perchlorate, sodium perchlorate, lithium chloride,
Thiocyan-9 lithium.

チオシアン酸カリウム、チオシアン酸ナトリウム。Potassium thiocyanate, sodium thiocyanate.

チオシアン峻セシウム、ホウフッ化リチウム、ホウフッ
化ナトリウム、フッ化リチウム、塩化リチウム、美化リ
チウム、ヨウ化リチウム、ヨウ化カリウム、ヨウ化ナト
リウム等が用いらハる。
Cesium thiocyanide, lithium borofluoride, sodium borofluoride, lithium fluoride, lithium chloride, lithium chloride, lithium iodide, potassium iodide, sodium iodide, etc. are used.

極性非プロトン溶媒として汀、アルカリ金属塩を溶解し
、熱可塑性樹脂と相溶性のあるものを1種以上用いるこ
とかで缶心。例えば炭酸プロピレン、炭酸エチレン、ジ
メチルホルムアミド、ジエチルホルムアミド、ジメチル
アセトアミド、N−メチルピロリドン、テトラメチルウ
レア、ヘキサメチルホスホルアミド、ジメチルスルホキ
シド。
The can core can be obtained by dissolving alkali metal salt as a polar aprotic solvent and using at least one solvent that is compatible with the thermoplastic resin. For example, propylene carbonate, ethylene carbonate, dimethylformamide, diethylformamide, dimethylacetamide, N-methylpyrrolidone, tetramethylurea, hexamethylphosphoramide, dimethylsulfoxide.

アセトニトリル、スルホラン等か用いらhる。Use acetonitrile, sulfolane, etc.

この発明の帯電防止性に潰れた樹脂組成物は射出成形法
、押出成形法、圧縮成形法あるいは真空成形法等の通常
の成形方法を用いて成形加工することがで傘る。
The antistatic resin composition of the present invention can be molded using a conventional molding method such as injection molding, extrusion molding, compression molding, or vacuum molding.

次にこの発明の樹脂組成物を夷角例にて具体的に説明す
る。
Next, the resin composition of the present invention will be specifically explained using an example of Ei angle.

実癩例1 炭酸プロピレン70電量部に過塙訴酸リチウム(無水)
30重緻部を80℃で攪拌りながら溶解させ透明な溶液
を得た。熱可塑性樹脂としてアクリル系樹脂であるアク
リベットS(三菱レイヨン)ヲ用い、この樹脂100軍
量部に回連のf?j液11Nit部を押出機を用いて1
80°Cで混練し、ペレタイザーによhベレットとした
。このペレットを射出成形機を用いて厚さ約3mmの板
状の試験片を作成し、スタチツクオネストメーターを用
いて@電圧の半減期を測定し、帯電防止性を判ボした。
Leprosy case 1 70 parts of propylene carbonate plus lithium oxide (anhydrous)
A clear solution was obtained by dissolving 30 parts of the solution while stirring at 80°C. Acryvet S (Mitsubishi Rayon), an acrylic resin, is used as the thermoplastic resin, and 100 parts of this resin is mixed with f? Using an extruder, 11Nit part of liquid J was added to 1
The mixture was kneaded at 80°C and made into pellets using a pelletizer. A plate-shaped test piece with a thickness of about 3 mm was prepared from the pellet using an injection molding machine, and the half-life of the voltage was measured using a static honest meter to determine the antistatic property.

結果を表1に示した。The results are shown in Table 1.

なお、スタテツクオ不ストメーターの測定条件は次の通
りである。
The measurement conditions of the static quotient are as follows.

印加電圧    10000V 試料回転数   130orpm 測定湿度    50%RH 測定副産    30”C 印加時間    1.0分 耐洗浄性は試料表[fiを中性況剤水溶液で充分洗浄し
た後、イオン交換水で充分洗浄し、その後室温で1週間
デシケータ中で乾燥した試料をスタチツクオネストメー
タを用いて帯電圧の半減期を測定した。結果と表1に示
した。
Applied voltage: 10,000 V Sample rotation speed: 130 orpm Measurement humidity: 50% RH Measurement by-product: 30"C Application time: 1.0 minutes After that, the sample was dried in a desiccator at room temperature for one week, and the half-life of the charged voltage was measured using a static honest meter.The results are shown in Table 1.

透F+J性は光礫透過率によって評価した。測定方法け
ASTM DIO03の方法を用い之。結果を表1に示
した。
Transparency F+J property was evaluated by optical gravel transmittance. The measurement method was ASTM DIO03. The results are shown in Table 1.

実権例2 実施例1と同様に炭酸プロピレン95mF鐘部、過塩素
酸リチウム(無水)5]if量部の溶液を調製し九〇ア
クリル系樹脂であるアクリペラI−V)] (三菱レイ
ヨン製)100重量部にこの溶液11重槍部を実症例1
と同様に混合し、試験片を作成した。帯電防止性、耐洗
浄性および透明性金実施列1と同様に評価した。結果を
表1に示した。
Practical Example 2 In the same manner as in Example 1, a solution containing 95 mF of propylene carbonate and 5 parts of lithium perchlorate (anhydrous) was prepared and 90 parts of acrylic resin Acrypera IV) (manufactured by Mitsubishi Rayon) was prepared. Add 11 parts of this solution to 100 parts by weight for actual case 1.
A test piece was prepared by mixing in the same manner as above. Antistatic properties, wash resistance, and transparency were evaluated in the same manner as in Gold Example 1. The results are shown in Table 1.

実権例3 実権例1と同様に炭酸プロピレン60重を部、過塩素酸
リチウム40M量部の浴′g!Lを調製した。この浴液
15重量部をアクリベットs 100重量部にニーダ−
を用いて混練し、圧縮成形により2mm厚の板状の試験
片を作成した。帯電防止性、耐洗浄性2よび透明性を実
権例1と同様に評価した。結果を表1に示した。
Practical Example 3 As in Practical Example 1, a bath containing 60 parts by weight of propylene carbonate and 40 M parts of lithium perchlorate was prepared. L was prepared. 15 parts by weight of this bath liquid was kneaded into 100 parts by weight of Acrybet S.
A 2 mm thick plate-shaped test piece was prepared by compression molding. Antistatic properties, wash resistance 2, and transparency were evaluated in the same manner as in Actual Example 1. The results are shown in Table 1.

実権例4 実加例3と同じ過塩素酸リチウムの炭酸プロピレンd/
[23重量部とアクリベット6100M量部と実権例3
と同様に混線し試験片を作成した。帝亀防止性、耐洗浄
性、透明性を実権例1と同様に評価した。結果を表1に
示した。
Practical example 4 Propylene carbonate d/ of lithium perchlorate same as practical example 3
[23 parts by weight and 6100M parts by weight of Acrybet and actual example 3
A test piece was prepared by mixing wires in the same manner as above. The anti-glare properties, wash resistance, and transparency were evaluated in the same manner as in Example 1. The results are shown in Table 1.

比較例1 アクリベット日に炭酸プロピレンおよび過塩素管リチウ
ム(無水)を加えることなく実権例1と同様な方法で試
験片を作成し帯電防止性、透明性を評価した。結果を表
1に示した。
Comparative Example 1 A test piece was prepared in the same manner as in Practical Example 1 without adding propylene carbonate and lithium perchlorate (anhydrous) to Acribet, and the antistatic properties and transparency were evaluated. The results are shown in Table 1.

比較例2 アクリベットθ100 li(置部、炭酸プロピレン1
゜重曖部の組成の試験片を実権例1と同様な方法で作成
し帯電防止性、透明性全評価した。結果を表1に示した
Comparative Example 2 Acrivet θ100 li (Okibe, propylene carbonate 1
A test piece having the composition of the heavy ambiguous area was prepared in the same manner as in Practical Example 1, and the antistatic property and transparency were completely evaluated. The results are shown in Table 1.

比較例3 アクリベット5loo]F量部、過塩素俊リチウム(無
水)5重量部の組成の試験片全実施例1と1同様な方法
で作成し帯電防止性、透明性全評価した。
Comparative Example 3 A test piece having a composition of 5 parts by weight of Acrybet 5loo] F and 5 parts by weight of lithium perchlorate (anhydrous) was prepared in the same manner as in Examples 1 and 1, and the antistatic properties and transparency were evaluated.

結果を表1に示した。The results are shown in Table 1.

表  1 実施例5 炭暇エチレン60車量部に過塩素管リチウム(無水)4
0車量部を約80°Cで攪拌しなから溶解させ逍#:!
AなfB液を得た。この溶液16 g蓋部をアクリベッ
トs 100 M置部にニーダーを用いて混練し、圧憚
成形により2mm厚の試験片を作成した。実抱例1と同
様に帯4防止性、耐洗浄性、透明性全評価した。結果・
f表2に示した。
Table 1 Example 5 Perchlorine tube lithium (anhydrous) 4 parts per 60 car parts of ethylene with charcoal
Dissolve 0 parts by stirring at approximately 80°C.
A fB solution was obtained. 16 g of this solution was kneaded in a lid part of Acryvet S 100 M using a kneader, and a test piece with a thickness of 2 mm was prepared by compression molding. In the same manner as Example 1, the band 4 prevention property, wash resistance, and transparency were all evaluated. result·
f is shown in Table 2.

Ji@Wす6 実施例5と同一の浴液23恵菫部とアクリベットθ10
0 jlj敏部の組成の試験片と実施例5と1間様に作
成し、帯電防止性、耐洗浄性、透(7)ヰを評価した。
Ji@Wsu 6 Same bath liquid 23 as in Example 5 Sumirebe and Acrybet θ10
A test piece having a composition of 0.0 jlj and Example 5 was prepared in the same manner as that of Example 5, and the antistatic properties, wash resistance, and transparency (7) were evaluated.

結果を表2に示した。The results are shown in Table 2.

表 2 表1及び表2に示すように、この発明の実癲例によるも
のけ、比較例に比べて低湿度vcおいても大巾に帝戒防
止効果か向上しており、洗浄してもその効果は低下しな
い。また、光線透過量も職安することなく、良好な透明
性を保持している。
Table 2 As shown in Tables 1 and 2, the Mononoke according to the practical example of the present invention has a significantly improved anti-imperial effect even in low humidity VC compared to the comparative example, and even after washing. Its effectiveness does not decrease. In addition, the amount of light transmitted does not decrease the quality of work, and it maintains good transparency.

〔発(7)の効果〕 この発明は以上説明したとおり、熱可塑性樹脂にアルカ
リ金属塩と極性非プロトン溶媒を営ませることにより、
低湿度の環境中においても艮好な帯戒防出効果を保ML
、洗浄によっても帯電防止性が低下しなA樹脂組成物か
寿ら苅る効果がある。
[Effect of (7)] As explained above, this invention provides a thermoplastic resin with an alkali metal salt and a polar aprotic solvent.
ML maintains excellent anti-seizure effect even in low-humidity environments.
The A resin composition has antistatic properties that do not deteriorate even after washing.

なお、熱可塑性樹脂としてアクリル系樹脂を用いhばア
クリル系樹脂の良好な透明性を保持する饗脂組成物か得
られる。
Note that if an acrylic resin is used as the thermoplastic resin, a resin composition that maintains the good transparency of the acrylic resin can be obtained.

Claims (3)

【特許請求の範囲】[Claims] (1)熱可塑性樹脂にアルカリ金属塩と極性非プロトン
溶媒を含ませた樹脂組成物。
(1) A resin composition in which a thermoplastic resin contains an alkali metal salt and a polar aprotic solvent.
(2)熱可塑性樹脂100重量部にアルカリ金属塩0.
1〜30重量部と極性非プロトン溶媒1〜30重量部を
含ませた特許請求の範囲第1項記載の樹脂組成物。
(2) 0.0% alkali metal salt per 100 parts by weight of thermoplastic resin.
The resin composition according to claim 1, which contains 1 to 30 parts by weight and 1 to 30 parts by weight of a polar aprotic solvent.
(3)熱可塑性樹脂はアクリル系樹脂である特許請求の
範囲第1項又は第2項記載の樹脂組成物。
(3) The resin composition according to claim 1 or 2, wherein the thermoplastic resin is an acrylic resin.
JP19616784A 1984-09-17 1984-09-17 Resin composition Pending JPS6172061A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP19616784A JPS6172061A (en) 1984-09-17 1984-09-17 Resin composition
DE3532805A DE3532805C2 (en) 1984-09-17 1985-09-13 Antistatic acrylic polymer composition
US06/776,885 US4687801A (en) 1984-09-17 1985-09-17 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19616784A JPS6172061A (en) 1984-09-17 1984-09-17 Resin composition

Publications (1)

Publication Number Publication Date
JPS6172061A true JPS6172061A (en) 1986-04-14

Family

ID=16353319

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19616784A Pending JPS6172061A (en) 1984-09-17 1984-09-17 Resin composition

Country Status (1)

Country Link
JP (1) JPS6172061A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001329253A (en) * 2000-03-14 2001-11-27 Kao Corp Antistatic agent composition
US6610766B1 (en) 1998-03-12 2003-08-26 Kureha Kagaku Kogyo K.K. Polyvinylidene fluoride resin composition
US6846436B1 (en) 1999-05-12 2005-01-25 Kureha Kagaku Kogyo K.K. Semiconductive polyvinylidene fluoride resin composition
JP2006226369A (en) * 2005-02-16 2006-08-31 Fuji Koki Corp Motor operated valve with reduction gear

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6610766B1 (en) 1998-03-12 2003-08-26 Kureha Kagaku Kogyo K.K. Polyvinylidene fluoride resin composition
US6846436B1 (en) 1999-05-12 2005-01-25 Kureha Kagaku Kogyo K.K. Semiconductive polyvinylidene fluoride resin composition
JP2001329253A (en) * 2000-03-14 2001-11-27 Kao Corp Antistatic agent composition
JP2006226369A (en) * 2005-02-16 2006-08-31 Fuji Koki Corp Motor operated valve with reduction gear

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