JPH05339559A - Antistatic agent excellent in transparency - Google Patents

Antistatic agent excellent in transparency

Info

Publication number
JPH05339559A
JPH05339559A JP14592292A JP14592292A JPH05339559A JP H05339559 A JPH05339559 A JP H05339559A JP 14592292 A JP14592292 A JP 14592292A JP 14592292 A JP14592292 A JP 14592292A JP H05339559 A JPH05339559 A JP H05339559A
Authority
JP
Japan
Prior art keywords
transparency
antistatic agent
acrylic
test piece
test
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
JP14592292A
Other languages
Japanese (ja)
Other versions
JP3375148B2 (en
Inventor
Kiyotaka Hamaguchi
精隆 浜口
Tetsuya Fujisawa
哲也 藤澤
Akira Fujii
昭 藤井
Toshiichi Fukunaga
登志一 福永
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.)
Tosoh Corp
Tosoh Silica Corp
Original Assignee
Nippon Silica Industrial Co Ltd
Tosoh 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 Nippon Silica Industrial Co Ltd, Tosoh Corp filed Critical Nippon Silica Industrial Co Ltd
Priority to JP14592292A priority Critical patent/JP3375148B2/en
Publication of JPH05339559A publication Critical patent/JPH05339559A/en
Application granted granted Critical
Publication of JP3375148B2 publication Critical patent/JP3375148B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain an antistatic agent which is excellent in transparency and user for making a resin film for food wrapping, etc., antistaic. CONSTITUTION:The title agent comprises a synthetic hectorite clay mineral contg. 1.0-10.0wt.% sodium pyrophosphate, an acrylic or polyolefin-based soap- free emulsion, and a surfactant of an acetylene glycol type.

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、菓子類や生鮮食品を包
装する食品包装材または一般的な包装フィルム等、透明
性が重視される樹脂フィルムの帯電防止剤に関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antistatic agent for a resin film, such as a food packaging material for packaging confectionery and fresh food, or a general packaging film, in which transparency is important.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】一般に
樹脂フィルム等のポリマー製品は1013Ωcmを上回る
体積固有抵抗及び1013Ωを上回る表面固有抵抗を有し
ておりその電気絶縁性は、ポリマー製品の特徴のひとつ
と言える。この特徴はポリマー製品の需要拡大に大きく
寄与してきたが、その反面帯電による静電気障害を生じ
ている。摩擦等によりいったん静電気を生じると電気絶
縁特性により外部に逃げにくく、蓄積し、様々な問題を
生ずる事になる。例えば食品包装材においては陳列中に
塵や埃が付着し、外見上、著しくその商品としての価値
を低下させている。このような問題を防止するために一
般に各種界面活性剤を樹脂に練り込むか塗布する方法が
実施されている(シーエムシー発行,ファインケミカ
ル,“帯電防止材 最近の市場動向(上)”Vol.1
6,No.15,P24〜P36,(1987))。
2. Description of the Related Art Generally, polymer products such as resin films have a volume resistivity of more than 10 13 Ωcm and a surface resistivity of more than 10 13 Ω. This is one of the features of the product. This feature has greatly contributed to the expansion of demand for polymer products, but on the other hand, it causes electrostatic damage due to electrification. Once static electricity is generated due to friction, etc., it is difficult for the static electricity to escape to the outside due to its electrical insulation properties, and it accumulates, causing various problems. For example, in food packaging materials, dust and dirt are attached during the display, and the value of the product is remarkably reduced in appearance. In order to prevent such problems, a method of kneading or applying various surfactants to a resin is generally practiced (CMC Publishing, Fine Chemicals, "Antistatic Materials Recent Market Trends (1)" Vol. 1).
6, No. 15, P24-P36, (1987)).

【0003】然しながら上記各種界面活性剤の内、アニ
オン性,ノニオン性界面活性剤においては、練り込み方
式,塗布方式のいかんに拘らず一般に1012Ω以上の表
面固有抵抗レベルであり充分な帯電防止効果は得られて
いない。
However, among the above-mentioned various surfactants, the anionic and nonionic surfactants generally have a surface specific resistance level of 10 12 Ω or more regardless of the kneading method or the coating method, and sufficient antistatic property is obtained. No effect has been obtained.

【0004】またカチオン性界面活性剤,両性界面活性
剤は、発ガン性の疑いをもたれた物質が多く人体に与え
る影響が危惧されるために好ましくない。
Further, cationic surfactants and amphoteric surfactants are not preferable because many substances suspected of being carcinogenic may affect the human body.

【0005】一方、コロイド状のシリカやアルミナ水溶
液,天然クレーの精製品等を表面に塗布する方法も知ら
れている。
On the other hand, there is also known a method of applying colloidal silica or alumina aqueous solution, a purified product of natural clay or the like on the surface.

【0006】然しながらこれらの無機化合物を表面に塗
布した樹脂フィルムにおいては、接着性に乏しく均一な
表面塗布が困難であるという問題を有している。また樹
脂フィルムに塗布するにはハジキの問題から界面活性剤
との併用が不可欠でありその相容性の低さにより経時に
よる凝集や沈降分離を生じ、作業性の悪化および凝集に
よる透明性の劣化のため透明な有機フィルムを処理する
には不都合である。
However, the resin film coated with these inorganic compounds on the surface has a problem that the adhesiveness is poor and uniform surface coating is difficult. In addition, in order to apply it to the resin film, it is indispensable to use it together with a surfactant due to the problem of cissing, and its poor compatibility causes aggregation and sedimentation over time, resulting in poor workability and deterioration of transparency due to aggregation. Therefore, it is inconvenient to process a transparent organic film.

【0007】前述した様に透明な有機フィルムの帯電防
止剤として帯電防止効果,接着性および透明性に優れた
帯電防止剤は未だ得られておらずかかる帯電防止剤が強
く要望されていた。
As described above, as an antistatic agent for a transparent organic film, an antistatic agent excellent in antistatic effect, adhesiveness and transparency has not yet been obtained, and such an antistatic agent has been strongly demanded.

【0008】[0008]

【課題を解決するための手段】本発明者らは帯電防止効
果に優れた樹脂フィルムの製造に関し鋭意研究を積み重
ねた結果、ピロリン酸ソーダを含有してなる合成ヘクト
ライト粘土鉱物を利用し、アクリル系ソープフリーエマ
ルジョン又はポリオレフィン系ソープフリーエマルジョ
ンを接着剤として用い、更にアセチレングリコール型界
面活性剤を用いることにより接着性および透明性に優れ
た帯電防止剤が得られる事を見い出し本発明を完成し
た。
Means for Solving the Problems As a result of intensive studies conducted by the present inventors on the production of a resin film having an excellent antistatic effect, as a result of utilizing a synthetic hectorite clay mineral containing sodium pyrophosphate, an acrylic The present invention has been completed by finding that an antistatic agent excellent in adhesiveness and transparency can be obtained by using a soap-based emulsion or a polyolefin-based soap-free emulsion as an adhesive and further using an acetylene glycol type surfactant.

【0009】本発明において用いる合成ヘクトライト粘
土鉱物は、以下の一般式
The synthetic hectorite clay mineral used in the present invention has the following general formula:

【0010】[0010]

【化1】 [Chemical 1]

【0011】を有したものであり、主な成分としてマグ
ネシウム,ケイ素,ナトリウム及び微量のリチウム,フ
ッ素からなり、且つピロリン酸ソーダを含有したもので
ある。優れた接着性,透明性,及び帯電防止効果を得る
には、ピロリン酸ソーダの含有量は合成ヘクトライト粘
土鉱物全成分中1.0乃至10.0wt%、より好まし
くは3.0乃至8.0wt%である。ピロリン酸ソーダ
の含有量が上記範囲未満では透明性及び帯電防止効果が
劣る。また上記範囲より過剰のピロリン酸ソーダを含有
すると塗布液の安定性が劣ると共に塗膜肌が悪くなる。
In addition, it is composed of magnesium, silicon, sodium and trace amounts of lithium and fluorine as main components, and also contains sodium pyrophosphate. In order to obtain excellent adhesiveness, transparency, and antistatic effect, the content of sodium pyrophosphate is 1.0 to 10.0 wt% in the total components of the synthetic hectorite clay mineral, more preferably 3.0 to 8. It is 0 wt%. When the content of sodium pyrophosphate is less than the above range, the transparency and antistatic effect are poor. Further, if the content of sodium pyrophosphate exceeds the above range, the stability of the coating solution becomes poor and the coating film surface becomes poor.

【0012】又、合成ヘクトライト粘土鉱物は本発明に
よる帯電防止剤の全成分中1乃至10wt%で使用され
得るが、使用量は帯電防止効果等の目的に応じて決定す
れば良い。但し1wt%以下の濃度では帯電防止効果が
得難く、また10wt%を越える濃度では粘度の上昇が
激しく作業性が悪くなるので注意を要する。
The synthetic hectorite clay mineral may be used in an amount of 1 to 10 wt% in all the components of the antistatic agent according to the present invention, and the amount used may be determined according to the purpose such as antistatic effect. However, it should be noted that the concentration of 1 wt% or less makes it difficult to obtain the antistatic effect, and the concentration of more than 10 wt% causes the viscosity to increase sharply and the workability to deteriorate.

【0013】次いで、用いる接着剤としては優れた透明
性を得る目的からアクリル系及びポリオレフィン系ソー
プフリーエマルジョンを使用するのが好ましい。これら
のアクリル系ソープフリーエマルジョンの内には、アク
リル酸エステル単独ポリマーやアクリル酸エステルとメ
タクリル酸エステル,酢酸ビニル,スチレン,アクリロ
ニトリル,アクリル酸等との共重合体なども含まれる。
また、ポリオレフィン系ソープフリーエマルジョンの内
には、エチレン酢酸ビニル共重合エマルジョン,エチレ
ンアクリル酸共重合体,アイオノマー等も含まれる。接
着剤としてのアクリル系及びポリオレフィン系ソープフ
リーエマルジョンの混合比率は広範囲に渡り可能で目的
とする接着強度に応じて使用すれば良いが、通常は全成
分中5.0乃至50wt%で用いることが好ましい。
Next, as the adhesive to be used, acrylic and polyolefin soap-free emulsions are preferably used for the purpose of obtaining excellent transparency. These acrylic soap-free emulsions also include acrylic acid ester homopolymers, copolymers of acrylic acid esters and methacrylic acid esters, vinyl acetate, styrene, acrylonitrile, acrylic acid, and the like.
Further, among the polyolefin-based soap-free emulsions, ethylene vinyl acetate copolymer emulsion, ethylene acrylic acid copolymer, ionomer and the like are also included. Acrylic and polyolefin soap-free emulsions as an adhesive can be mixed in a wide range and may be used according to the intended adhesive strength, but usually 5.0 to 50 wt% of all components is used. preferable.

【0014】接着剤として乳化剤含有アクリルエマルジ
ョン,あるいはカルボキシメチルセルロース(CM
C),ポリビニルアルコール等、他の水溶性樹脂の使用
は透明性,接着性,帯電防止等の性能に劣る場合があり
好ましくない。
Acrylic emulsion containing emulsifier or carboxymethyl cellulose (CM
The use of other water-soluble resins such as C) and polyvinyl alcohol may be inferior in performance such as transparency, adhesiveness and antistatic property, which is not preferable.

【0015】さらに本発明における界面活性剤は優れた
ハジキ防止効果および優れた系の安定性からアセチレン
グリコール型界面活性剤を使用する。このアセチレング
リコール型界面活性剤は分子中にアセチレン結合とアル
コール性水酸基とを持つ一連の化合物であり酸化エチレ
ン等の付加体をも含むものである。かかるアセチレング
リコール型界面活性剤は樹脂フィルムに帯電防止剤を塗
布する時におこるハジキを防ぐ目的で添加するため、添
加は必要最小量でよく全成分中0.1乃至5wt%で用
いれば良い。
Further, as the surfactant in the present invention, an acetylene glycol type surfactant is used because of its excellent cissing prevention effect and excellent system stability. This acetylene glycol type surfactant is a series of compounds having an acetylene bond and an alcoholic hydroxyl group in the molecule and also includes an adduct such as ethylene oxide. Since such an acetylene glycol type surfactant is added for the purpose of preventing cissing that occurs when the antistatic agent is applied to the resin film, the addition amount may be the minimum necessary amount and may be 0.1 to 5 wt% of all components.

【0016】他のノニオン系界面活性剤,アニオン系界
面活性剤は経時により粘度の上昇や沈澱物の生成等、問
題を生じる事もあり好ましくない。
Other nonionic surfactants and anionic surfactants are not preferable because they may cause problems such as increase in viscosity and formation of precipitates over time.

【0017】カチオン性界面活性剤,両性界面活性剤
は、発ガン性の疑いをもたれた物質が多く人体に与える
影響が危惧されるために好ましくないと共に合成ヘクト
ライト粘土鉱物の分散阻害を起こすために使用出来な
い。
Cationic surfactants and amphoteric surfactants are not preferable because many substances suspected to have carcinogenic effects on the human body are unfavorable and they also cause dispersion inhibition of synthetic hectorite clay minerals. It cannot be used.

【0018】[0018]

【実施例】以下本発明を、実施例および比較例をあげて
更に詳細に説明する。なお有機フィルムへの塗布および
電気特性,透過率の測定は以下の方法に従って実施し
た。 (有機フィルムへの塗布,乾燥)調整後の帯電防止剤を
適量有機フィルムに滴下し膜厚約2.5ミクロンの均一
な塗膜を得るためにNo.5バーコーターにより塗布
後、常温で乾燥しテストピースとした。
EXAMPLES The present invention will be described in more detail with reference to Examples and Comparative Examples. The coating on the organic film and the measurement of electrical characteristics and transmittance were carried out according to the following methods. (Applying to organic film, drying) An appropriate amount of the adjusted antistatic agent was dropped onto the organic film to obtain a uniform coating film having a thickness of about 2.5 μm. After coating with a 5-bar coater, the test piece was dried at room temperature.

【0019】(電気特性の測定)4329A HIGH
RESISTANCE METER(横河ヒューレッ
トパッカード社製)を用い表面固有抵抗を測定した。
(Measurement of electrical characteristics) 4329A HIGH
The surface resistivity was measured using a RESISTANCE METER (manufactured by Yokogawa Hewlett-Packard Co.).

【0020】(透過率の測定)MSC−CH型測色計
(スガ試験株式会社製)を用い透過率を測定した。測定
方法は、ブランクとして有機フィルムをガラス板に貼り
付けた時の透過率を100%と設定し、次にテストピー
スをガラス板に貼り付け同様の操作を行い透過率を測定
した。
(Measurement of Transmittance) An MSC-CH colorimeter (manufactured by Suga Test Co., Ltd.) was used to measure the transmittance. As the measuring method, the transmittance when the organic film was stuck on the glass plate as a blank was set to 100%, and then the test piece was stuck on the glass plate and the same operation was performed to measure the transmittance.

【0021】(接着性の測定)ゴムの剥離試験(JIS
K6301−1962)に基ずき試験を実施した。テ
ストピースの塗膜面に市販のセロハンテープ(日東セロ
ハン社製)7.5cm×5.0cmをローラーを用い貼
り付けた後、90°剥離しその時にかかるトルクを測定
し、以下の計算式により接着強さを算出した。
(Measurement of Adhesiveness) Rubber Peeling Test (JIS
Based on K6301-1964), the pedestrian test was carried out. Commercially available cellophane tape (manufactured by Nitto Cellophane Co., Ltd.) 7.5 cm x 5.0 cm was attached to the coating surface of the test piece using a roller, peeled at 90 °, and the torque applied at that time was measured. The adhesive strength was calculated.

【0022】Tf=F/b Tf:接着強さ(kg/cm) F:剥離荷重(kg) b:試験片の幅(cm) 接着強さが100g/cm以上で接着性;〇、未満を接
着性;×とした。
Tf = F / b Tf: Adhesive strength (kg / cm) F: Peeling load (kg) b: Width of test piece (cm) Adhesive strength of 100 g / cm or more; Adhesiveness: rated as x.

【0023】(塗膜状態)目視により塗膜状態を観察し
分散状態,塗膜肌等を評価した。
(Coating state) The coating state was visually observed to evaluate the dispersion state, coating surface and the like.

【0024】(塗布液の安定性)常温で30日放置し、
目視により塗布液の状態を観察した。
(Stability of coating liquid) Leave at room temperature for 30 days,
The state of the coating liquid was visually observed.

【0025】実施例1 水90重量部、ピロリン酸ソーダ6wt%含有の合成ヘ
クトライト粘土鉱物(商品名ラポナイトS:Lapor
te Industries Ltd.製)10重量
部、アクリル系ソープフリーエマルジョン(商品名アル
マテックスE−269:三井東圧化学社製)30重量
部、アセチレングリコール型界面活性剤(商品名サーフ
ィノール440:日信化学社製)1重量部を、ハイ・ス
ピード・ミキサーにより充分に撹拌混合し塗布液を調整
した後、前記塗布方法に従いPPフィルムに塗布してテ
ストピースとし、各種評価試験を実施した。結果を第一
表に示した。
Example 1 A synthetic hectorite clay mineral containing 90 parts by weight of water and 6 wt% of sodium pyrophosphate (trade name: Laponite S: Lapor)
te Industries Ltd. 10 parts by weight, acrylic soap-free emulsion (trade name Almatex E-269: manufactured by Mitsui Toatsu Chemicals, Inc.) 30 parts by weight, acetylene glycol type surfactant (trade name Surfynol 440: manufactured by Nisshin Chemical Co., Ltd.) 1 part by weight was sufficiently agitated and mixed by a high speed mixer to prepare a coating solution, which was then coated on a PP film according to the coating method described above to prepare a test piece, and various evaluation tests were carried out. The results are shown in Table 1.

【0026】実施例2 実施例1で使用した水溶性アクリル系エマルジョンの代
わりにポリオレフィン系エマルジョン(商品名:ケミパ
ールS−100:三井石油化学社製)を使用し、後は同
様の条件によりテストピースを得て、各種評価試験を実
施した。結果を第一表に示した。
Example 2 Instead of the water-soluble acrylic emulsion used in Example 1, a polyolefin emulsion (trade name: Chemipearl S-100: manufactured by Mitsui Petrochemical Co., Ltd.) was used, and the test piece was then subjected to the same conditions. Then, various evaluation tests were carried out. The results are shown in Table 1.

【0027】実施例3 実施例1で使用した合成ヘクトライト粘土鉱物の配合量
を5重量部に変更し、後は同様の条件によりテストピー
スを得て、各種評価試験を実施した。結果を第一表に示
した。
Example 3 The compounding amount of the synthetic hectorite clay mineral used in Example 1 was changed to 5 parts by weight, and thereafter, test pieces were obtained under the same conditions and various evaluation tests were carried out. The results are shown in Table 1.

【0028】実施例4 実施例1でピロリン酸ソーダ9%含有の合成ヘクトライ
ト粘土鉱物を使用し、後は同様の条件によりテストピー
スを得て、各種評価試験を実施した。結果を第一表に示
した。
Example 4 The synthetic hectorite clay mineral containing 9% of sodium pyrophosphate was used in Example 1, and thereafter a test piece was obtained under the same conditions and various evaluation tests were carried out. The results are shown in Table 1.

【0029】実施例5 実施例1で使用した水溶性アクリル系エマルジョンの配
合量を50重量部に変更し、後は同様の条件によりテス
トピースを得て、各種評価試験を実施した。結果を第一
表に示した。
Example 5 The amount of the water-soluble acrylic emulsion used in Example 1 was changed to 50 parts by weight, and thereafter a test piece was obtained under the same conditions, and various evaluation tests were carried out. The results are shown in Table 1.

【0030】比較例1 実施例1の合成ヘクトライト粘土鉱物を除いた配合で後
は同様の条件によりテストピースを得て、実施例1と同
様の試験を行い比較した結果を第一表に示した。
Comparative Example 1 A test piece was prepared under the same conditions except that the synthetic hectorite clay mineral of Example 1 was omitted, and the same test as in Example 1 was carried out. The comparison results are shown in Table 1. It was

【0031】比較例2 実施例1のアクリル系ソープフリーエマルジョンを除い
た配合で、後は同様の条件によりテストピースを得て、
実施例1と同様の試験を行い比較した結果を第一表に示
した。
Comparative Example 2 A test piece was obtained with the same composition as in Example 1 except that the acrylic soap-free emulsion was removed, and then the same conditions were used.
The same test as in Example 1 was performed and the results of comparison are shown in Table 1.

【0032】比較例3 実施例1のアセチレングリコール型界面活性剤を除いた
配合で、後は同様の条件によりテストピースを得て、実
施例1と同様の試験を行い比較した結果を第一表に示し
た。
Comparative Example 3 A test piece was obtained under the same conditions as in Example 1 except that the acetylene glycol type surfactant was removed, and the same test as in Example 1 was carried out. It was shown to.

【0033】比較例4 実施例1の配合で合成ヘクトライト粘土鉱物としてラポ
ナイトB(Laporte Industries L
td.製:ピロリン酸ソーダを含有しない)を使用し、
他の操作は同様に行いテストピースを得て、実施例1と
同様の試験を行い比較した結果を第一表に示した。
Comparative Example 4 Laponite B (Laporte Industries L) was used as a synthetic hectorite clay mineral with the composition of Example 1.
td. Made: does not contain sodium pyrophosphate),
Other operations were performed in the same manner to obtain a test piece, the same test as in Example 1 was performed, and the comparison results are shown in Table 1.

【0034】比較例5 実施例1の配合で合成ヘクトライト粘土鉱物としてピロ
リン酸ソーダを15重量部含有する合成ヘクトライト粘
土鉱物を使用し、他の操作は同様に行いテストピースを
得て、実施例1と同様の試験を行い比較した結果を第一
表に示した。
Comparative Example 5 A synthetic hectorite clay mineral containing 15 parts by weight of sodium pyrophosphate was used as the synthetic hectorite clay mineral in the composition of Example 1, and other operations were carried out in the same manner to obtain a test piece, and the test was carried out. The same test as in Example 1 was performed and the results of comparison are shown in Table 1.

【0035】比較例6 実施例1の配合でアクリル系ソープフリーエマルジョン
の代わりに乳化剤含有アクリルエマルジョン(商品名ボ
ンコートEC−100:大日本インキ化学社製)を使用
し、他の操作は同様に行いテストピースを得て、実施例
1と同様の試験を行い比較した結果を第一表に示した。
Comparative Example 6 Instead of the acrylic soap-free emulsion in the formulation of Example 1, an emulsifier-containing acrylic emulsion (Boncoat EC-100, trade name, manufactured by Dainippon Ink and Chemicals, Inc.) was used, and other operations were performed in the same manner. The test pieces were obtained, the same tests as in Example 1 were performed, and the results of comparison were shown in Table 1.

【0036】比較例7 実施例1の配合でアクリル系ソープフリーエマルジョン
の代わりにCMC(1%水溶液)(商品名CMC128
0:ダイセル化学社製)を使用し、他の操作は同様に行
いテストピースを得て、実施例1と同様の試験を行い比
較した結果を第一表に示した。
Comparative Example 7 The composition of Example 1 was replaced by CMC (1% aqueous solution) (trade name CMC128) instead of the acrylic soap-free emulsion.
(0: manufactured by Daicel Chemical Industries, Ltd.) and other operations were performed in the same manner to obtain a test piece, and the same test as in Example 1 was performed and the results of comparison are shown in Table 1.

【0037】比較例8 実施例1の配合でアクリル系ソープフリーエマルジョン
の代わりにPVA(5%水溶液)(商品名PVA(重合
度500):キシダ化学社製)を使用し、他の操作は同
様に行いテストピースを得て、実施例1と同様の試験を
行い比較した結果を第一表に示した。
Comparative Example 8 PVA (5% aqueous solution) (trade name PVA (polymerization degree 500): manufactured by Kishida Chemical Co., Ltd.) was used in place of the acrylic soap-free emulsion in the formulation of Example 1, and other operations were the same. Table 1 shows the comparison results obtained by performing the same test as in Example 1 to obtain a test piece.

【0038】比較例9 実施例1の配合で界面活性剤としてノニオン系のラウリ
ルエーテル型界面活性剤(商品名ノニオンP208:日
本油脂社製)を使用し、他の操作は同様に行いテストピ
ースを得て、実施例1と同様の試験を行い比較した結果
を第一表に示した。
Comparative Example 9 A nonionic lauryl ether type surfactant (trade name: Nonion P208, manufactured by NOF CORPORATION) was used as a surfactant in the formulation of Example 1, and other operations were carried out in the same manner to prepare a test piece. The same tests as in Example 1 were performed and the results of comparison were shown in Table 1.

【0039】比較例10 実施例1の配合で界面活性剤としてアニオン系界面活性
剤(ラウリル硫酸ナトリウム)を使用し、他の操作は同
様に行いテストピースを得て、実施例1と同様の試験を
行い比較した結果を第一表に示した。
Comparative Example 10 An anionic surfactant (sodium lauryl sulfate) was used as a surfactant in the formulation of Example 1, and other operations were performed in the same manner to obtain a test piece, and the same test as in Example 1 was performed. The results are shown in Table 1.

【0040】比較例11 実施例1の配合で界面活性剤としてカチオン系界面活性
剤(商品名コータミン24P:花王社製)を使用し、他
の操作は同様に行いテストピースを得て、実施例1と同
様の試験を行い比較した結果を第一表に示した。
Comparative Example 11 In the formulation of Example 1, a cationic surfactant (trade name: Kotamine 24P: manufactured by Kao Corporation) was used as a surfactant, and other operations were performed in the same manner to obtain a test piece. The same test as in Example 1 was conducted and the results of comparison are shown in Table 1.

【0041】比較例12 実施例1の配合で合成ヘクトライト粘土のかわりに天然
ベントナイト精製品(商品名クニピアF:クニミネ工業
社製)を使用し、他の操作は同様に行いテストピースを
得て、実施例1と同様の試験を行い比較した結果を第一
表に示した。
Comparative Example 12 A natural bentonite refined product (trade name: Kunipia F: manufactured by Kunimine Industry Co., Ltd.) was used in place of the synthetic hectorite clay in the composition of Example 1, and other operations were performed in the same manner to obtain a test piece. The same test as in Example 1 was performed and the results of comparison are shown in Table 1.

【0042】[0042]

【表1】 [Table 1]

【0043】[0043]

【発明の効果】以上の説明から明らかなように、本発明
によれば樹脂フィルムに対し十分な帯電防止効果を与え
ると共に接着性及び透明性に優れた帯電防止剤を提供す
ることが可能である。
As is apparent from the above description, according to the present invention, it is possible to provide an antistatic agent which gives a resin film a sufficient antistatic effect and is excellent in adhesiveness and transparency. ..

───────────────────────────────────────────────────── フロントページの続き (72)発明者 福永 登志一 山口県徳山市大字大島76−3 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Toshikazu Fukunaga 76-3 Oshima, Tokuyama City, Yamaguchi Prefecture

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ピロリン酸ソーダを1.0乃至10wt
%含有してなる合成ヘクトライト粘土鉱物、アクリル系
又はポリオレフィン系ソープフリーエマルジョン、及び
アセチレングリコール型界面活性剤からなる透明性に優
れた帯電防止剤。
1. Sodium pyrophosphate is 1.0 to 10 wt.
%, An antistatic agent having excellent transparency, which comprises a synthetic hectorite clay mineral, an acrylic or polyolefin soap-free emulsion, and an acetylene glycol type surfactant.
JP14592292A 1992-06-05 1992-06-05 Antistatic agent with excellent transparency Expired - Fee Related JP3375148B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14592292A JP3375148B2 (en) 1992-06-05 1992-06-05 Antistatic agent with excellent transparency

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14592292A JP3375148B2 (en) 1992-06-05 1992-06-05 Antistatic agent with excellent transparency

Publications (2)

Publication Number Publication Date
JPH05339559A true JPH05339559A (en) 1993-12-21
JP3375148B2 JP3375148B2 (en) 2003-02-10

Family

ID=15396188

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14592292A Expired - Fee Related JP3375148B2 (en) 1992-06-05 1992-06-05 Antistatic agent with excellent transparency

Country Status (1)

Country Link
JP (1) JP3375148B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2303374A (en) * 1995-07-18 1997-02-19 Laporte Industries Ltd Surface coating composition
JP2015199535A (en) * 2014-04-10 2015-11-12 電気化学工業株式会社 cover film

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2303374A (en) * 1995-07-18 1997-02-19 Laporte Industries Ltd Surface coating composition
GB2303373A (en) * 1995-07-18 1997-02-19 Laporte Industries Ltd Surface coating composition
JP2015199535A (en) * 2014-04-10 2015-11-12 電気化学工業株式会社 cover film

Also Published As

Publication number Publication date
JP3375148B2 (en) 2003-02-10

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