JPH034578B2 - - Google Patents
Info
- Publication number
- JPH034578B2 JPH034578B2 JP61038685A JP3868586A JPH034578B2 JP H034578 B2 JPH034578 B2 JP H034578B2 JP 61038685 A JP61038685 A JP 61038685A JP 3868586 A JP3868586 A JP 3868586A JP H034578 B2 JPH034578 B2 JP H034578B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl group
- carbon atoms
- good
- ratio
- printability
- 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 - Lifetime
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 239000002216 antistatic agent Substances 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- -1 alkyl diethanolamine Chemical compound 0.000 claims description 7
- 229920000098 polyolefin Polymers 0.000 claims description 7
- 238000004898 kneading Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 description 9
- 230000002950 deficient Effects 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000002087 whitening effect Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000007786 electrostatic charging Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
〔産業上の利用分野〕
本発明は、ポリオレフイン用帯電防止剤に関す
るものである。
〔従来の技術及び問題点〕
一般にポリオレフインはポリエチレン、ポリプ
ロピレン等の総称であり、フイルム、成形品、繊
維などの成形材料として広く用いられている。こ
れらは、通常、優れた電気絶縁性を有している半
面、静電気が帯電、蓄積し易く、種々の障害や災
害の原因となることがある。例えば周知のよう
に、これらの成形物は、静電気帯電により極めて
汚染され易く、汚れが強固に付着して商品価値を
著しく低下させる原因となる。また放電火花によ
る可燃性ガスの引火爆発も大きい問題である。
これらの問題を解決するため、従来、帯電防止
剤が提案されているが、帯電防止効果の持続性及
び成形品の表面状態の良好なこと（白化現象のな
いこと、ベタツキのないこと）及び印刷性の良好
なことを同時に満足するという点で充分ではなか
つた。
〔問題点を解決するための手段〕
本発明者らは、これらポリオレフインの持つ汚
れ易さ、可燃性ガスの誘引爆発の可能性をなく
し、且つこの効果を持続せしめ、表面状態の良好
な、また、印刷適性に優れたポリオレフイン組成
物を与える帯電防止剤を得るべく鋭意検討した結
果、特定の化学物質を特定の割合で用いた時、こ
れらを満足できることを見い出して本発明を完成
した。
即ち、本発明は下記の一般式
（式中、R1は炭素数16と18のアルキル基を表
わし、炭素数16と18のアルキル基が40／60〜20／
80の比で存在する。）
で表わされるアルキルジエタノールアミンと
下記の一般式
R2OH (2)
（式中、R2は炭素数16と18のアルキル基を表
わし、炭素数16と18のアルキル基が40／60〜20／
80の比で存在する。）
で表わされる高級アルコールからなり、アルキル
ジエタノールアミン(1)と高級アルコール(2)の重量
比が30／70〜70／30であるポリオレフイン用帯電
防止剤を提供するものである。
本発明に係る帯電防止剤をポリオレフイン樹脂
に練り込めば、帯電防止効果の持続性、成形品に
表面状態、印刷性の点で極めて満足すべき結果が
得られる。
本発明によればアルキルジエタノールアミンと
高級アルコールとを組み合わせて用いると予想外
にも各々の化合物のアルキル鎖長の影響が非常に
大きいことがわかつた。
表１にアルキルジエタノールアミンと高級アル
コールとの比が50：50の場合のアルキル鎖長の影
響を示したが、表１に於いて、次の様な傾向が認
められた。
領域……帯電防止効果持続性 不良
成形品の表面状態 ベトツキ傾向あり
印刷性 不良
領域……帯電防止効果持続性 良好〜やや不良
成形品の表面状態 ベトツキ傾向あり
印刷性 不良
領域……帯電防止効果持続性 良好〜やや不良
成形品の表面状態 白化傾向あり
印刷性 不良
領域……帯電防止効果持続性 良好
成形品の表面状態 良好
印刷性 良好
即ち、前記のジエタノールアミンのアルキル基
R1、高級アルコールのアルキル基R2は谷炭素数
16と18とのものが40／60〜20／80でなければなら
ない。
[Industrial Application Field] The present invention relates to an antistatic agent for polyolefins. [Prior Art and Problems] Generally, polyolefin is a general term for polyethylene, polypropylene, etc., and is widely used as a molding material for films, molded products, fibers, etc. Although these materials usually have excellent electrical insulation properties, they tend to be charged and accumulate static electricity, which may cause various problems and disasters. For example, as is well known, these molded products are extremely susceptible to being contaminated by electrostatic charging, and dirt adheres firmly to them, causing a significant decrease in commercial value. Furthermore, ignition and explosion of flammable gas caused by discharge sparks is also a major problem. To solve these problems, antistatic agents have been proposed in the past, but they require long-lasting antistatic effects, good surface condition of molded products (no whitening phenomenon, no stickiness), and printing. It was not sufficient to simultaneously satisfy the requirements of good sex. [Means for Solving the Problems] The present inventors have solved the staining properties of these polyolefins and the possibility of combustible gas-induced explosions, sustained this effect, and produced polyolefins with good surface conditions and As a result of intensive studies to obtain an antistatic agent that provides a polyolefin composition with excellent printability, the present invention was completed by discovering that these can be satisfied when specific chemical substances are used in a specific ratio. That is, the present invention is based on the following general formula (In the formula, R 1 represents an alkyl group having 16 and 18 carbon atoms, and the alkyl group having 16 and 18 carbon atoms is 40/60 to 20/
Exist in a ratio of 80. ) and the following general formula R 2 OH (2) (wherein, R 2 represents an alkyl group having 16 and 18 carbon atoms, and the alkyl group having 16 and 18 carbon atoms is 40/60 to 20/
Exist in a ratio of 80. The present invention provides an antistatic agent for polyolefins, which is made of a higher alcohol represented by the following formula and has a weight ratio of alkyldiethanolamine (1) to higher alcohol (2) of 30/70 to 70/30. If the antistatic agent according to the present invention is mixed into a polyolefin resin, extremely satisfactory results can be obtained in terms of the sustainability of the antistatic effect, the surface condition of the molded product, and the printability. According to the present invention, it has been found that when an alkyl diethanolamine and a higher alcohol are used in combination, the influence of the alkyl chain length of each compound is unexpectedly large. Table 1 shows the influence of alkyl chain length when the ratio of alkyl diethanolamine to higher alcohol is 50:50, and the following trends were observed in Table 1. Area...Durability of antistatic effect Surface condition of defective molded product Printability with a tendency to stickiness Defective area...Durability of antistatic effect Good to slightly defective surface condition of molded product Printability with a tendency to stickiness Defective area...Duration of antistatic effect Good to slightly poor Surface condition of molded product Tendency to whitening Printability Poor area...Durability of antistatic effect Surface condition of good molded product Good printability Good In other words, the alkyl group of diethanolamine mentioned above
R 1 , alkyl group R 2 of higher alcohol has valley carbon number
16 and 18 must be between 40/60 and 20/80.
【表】【table】
次に実施例にて本発明を説明するが、本発明は
これらの実施例に限定されるものではない。
実施例・比較例 １
合成樹脂に対して表２に示す帯電防止剤を添加
してヘンシエルミキサーにて１分間混合撹拌す
る。そのあと、射出成形機（シリンダー温度200
〜250℃）にて、帯電防止剤を含有するプレート
（縦120mm、横60mm、厚み３mm）を射出成形して、
そのプレートの帯電防止効果、表面状態、印刷性
を30日後に調べた。帯電防止効果は表面固有抵抗
値（Ω／□）を測定（ASTM Ｄ 257）するこ
とにより判定した。その値が1010以下の場合良
好、1011〜1013はやや良好、1014以上は不良であ
る。表面状態は目視にて判定した。印刷性につい
ては次に様に行つた。テストプレーヤ上に、横
200mm×縦200mmの正方形にポリアミド系インキを
塗工して、その後横１mm×縦１mmの正方形が100
個できる様にカツターで傷をつける。その上に粘
着テープを貼り、ついでそれを剥離することによ
り半定した（JIS Ｋ−5400 1979）。インキが98％
以上残つている場合は良好、97％以下の場合は不
良と判定した。
ポリプロピレン（三井東圧Ｊ−109G）100部に
対して帯電防止剤を0.5部（アミン／アルコール
＝50／50（重量比））添加した場合の結果を表２に
示した。
尚、帯電防止剤無添加の場合のポリプロピレン
プレートの表面固有抵抗は1016Ω／□以上であ
り、表面状態、印刷性とも良好であつた。
Next, the present invention will be explained with reference to Examples, but the present invention is not limited to these Examples. Examples/Comparative Examples 1 The antistatic agent shown in Table 2 was added to the synthetic resin and mixed and stirred for 1 minute using a Henschel mixer. After that, the injection molding machine (cylinder temperature 200
A plate (120 mm long, 60 mm wide, 3 mm thick) containing an antistatic agent was injection molded at ~250℃).
The antistatic effect, surface condition, and printability of the plate were examined after 30 days. The antistatic effect was determined by measuring the surface resistivity (Ω/□) (ASTM D 257). A value of 10 10 or less is good, a value of 10 11 to 10 13 is somewhat good, and a value of 10 14 or more is bad. The surface condition was visually determined. Printability was examined as follows. On the test player, horizontally.
Coat a square of 200 mm x 200 mm in height with polyamide ink, then print 100 squares of 1 mm in width x 1 mm in height.
Cut it with a cutter so that you can separate it into pieces. Semi-fixation was achieved by applying an adhesive tape thereon and then peeling it off (JIS K-5400 1979). 98% ink
If it remained above 97%, it was judged as good, and if it remained below 97%, it was judged as bad. Table 2 shows the results when 0.5 part of an antistatic agent (amine/alcohol = 50/50 (weight ratio)) was added to 100 parts of polypropylene (Mitsui Toatsu J-109G). The surface resistivity of the polypropylene plate without the addition of antistatic agent was 10 16 Ω/□ or more, and both the surface condition and printability were good.
【表】【table】
【表】【table】
【表】
比較例 ２
帯電防止剤の組成をアミン／アルコール＝80〜
20（重量比）とした以外は実施例と同様に試験を
行つた。その結果を表３に示した。[Table] Comparative Example 2 The composition of the antistatic agent is amine/alcohol = 80~
The test was conducted in the same manner as in the example except that the weight ratio was 20 (weight ratio). The results are shown in Table 3.
【表】【table】
【表】【table】
Claims (1)
わし、炭素数16と18のアルキル基が40／60〜20／
80の比で存在する。） で表わされるアルキルジエタノールアミンと下記
一般式 R2OH (2) （式中、R2は炭素数16と18のアルキル基を表
わし、炭素数16と18のアルキル基が40／60〜20／
80の比で存在する。） で表わされる高級アルコールからなり、アルキル
ジエタノールアミン(1)と高級アルコール(2)の重量
比が30／70〜70／30であるポリオレフイン用練込
型帯電防止剤。[Claims] 1. The following general formula (In the formula, R 1 represents an alkyl group having 16 and 18 carbon atoms, and the alkyl group having 16 and 18 carbon atoms is 40/60 to 20/
Exist in a ratio of 80. ) and the following general formula R 2 OH (2) (wherein, R 2 represents an alkyl group having 16 and 18 carbon atoms, and the alkyl group having 16 and 18 carbon atoms is 40/60 to 20/
Exist in a ratio of 80. ) A kneading type antistatic agent for polyolefin, which is made of a higher alcohol represented by the following formula, and has a weight ratio of alkyl diethanolamine (1) to higher alcohol (2) of 30/70 to 70/30.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3868586A JPS62197434A (en) | 1986-02-24 | 1986-02-24 | Antistatic agent for polyolefin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3868586A JPS62197434A (en) | 1986-02-24 | 1986-02-24 | Antistatic agent for polyolefin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62197434A JPS62197434A (en) | 1987-09-01 |
| JPH034578B2 true JPH034578B2 (en) | 1991-01-23 |
Family
ID=12532145
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3868586A Granted JPS62197434A (en) | 1986-02-24 | 1986-02-24 | Antistatic agent for polyolefin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62197434A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62295936A (en) * | 1986-06-16 | 1987-12-23 | Kao Corp | Antistatic agent for polyolefin |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5879044A (en) * | 1981-11-06 | 1983-05-12 | Mitsui Toatsu Chem Inc | Resin composition for polypropylene film having improved fog resistance |
| JPS6128537A (en) * | 1984-07-18 | 1986-02-08 | Kao Corp | Antistatic agent for polyolefin resin |
-
1986
- 1986-02-24 JP JP3868586A patent/JPS62197434A/en active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5879044A (en) * | 1981-11-06 | 1983-05-12 | Mitsui Toatsu Chem Inc | Resin composition for polypropylene film having improved fog resistance |
| JPS6128537A (en) * | 1984-07-18 | 1986-02-08 | Kao Corp | Antistatic agent for polyolefin resin |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62197434A (en) | 1987-09-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4976741A (en) | Antistatic agent: mixture of anionic surfactant and a fluorine-containing nonionic surfactant | |
| US5863466A (en) | Electrostatic dissipative composition | |
| WO1998035359A9 (en) | Electrostatic dissipative composition | |
| US3485786A (en) | Antistatic polyolefins | |
| JP3874796B2 (en) | Thermally stable antistatic agent | |
| CA1256629A (en) | Electrically conductive plastics and production of same | |
| US3317505A (en) | Polyolefin compositions | |
| JPH0443104B2 (en) | ||
| JPH034578B2 (en) | ||
| JPS6057461B2 (en) | Method for producing biaxially stretched polypropylene film with improved antistatic properties | |
| JPH0236620B2 (en) | GOSEIJUSHOTAIDENBOSHIZAISOSEIBUTSU | |
| JPS6262836A (en) | Master pellet for antistatic resin | |
| US3395137A (en) | Process for rendering high molecular weight compounds resistant to electrostatic charge | |
| JPS5879042A (en) | Polyolefin film | |
| JPH0341100B2 (en) | ||
| US3321456A (en) | Polyolefin compositions | |
| JPH034579B2 (en) | ||
| JPS6254737A (en) | Additive composition for synthetic resin | |
| JPH0280488A (en) | Antistatic agent | |
| JPS63213538A (en) | Polyolefin resin composition for injection molding | |
| JPH08134289A (en) | Antistatic agent composition for polypropylene | |
| JPS62143956A (en) | Antistatic agent for styrenic resin | |
| JP3871227B2 (en) | Antistatic agent and antistatic resin composition containing the same | |
| JPS60199062A (en) | Antistatic conductive resin composition | |
| JPS62240343A (en) | Antistatic agent for styrene resin |