JPH08127694A - Pvc plastisol composition - Google Patents

Pvc plastisol composition

Info

Publication number
JPH08127694A
JPH08127694A JP28914494A JP28914494A JPH08127694A JP H08127694 A JPH08127694 A JP H08127694A JP 28914494 A JP28914494 A JP 28914494A JP 28914494 A JP28914494 A JP 28914494A JP H08127694 A JPH08127694 A JP H08127694A
Authority
JP
Japan
Prior art keywords
plasticizer
pts
pvc
polymerization inhibitor
plastisol composition
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
JP28914494A
Other languages
Japanese (ja)
Inventor
Tadashi Takahashi
忠 高橋
Koichi Ogawa
晃一 小川
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.)
Uchiyama Manufacturing Corp
Original Assignee
Uchiyama Manufacturing 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 Uchiyama Manufacturing Corp filed Critical Uchiyama Manufacturing Corp
Priority to JP28914494A priority Critical patent/JPH08127694A/en
Publication of JPH08127694A publication Critical patent/JPH08127694A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Organic Insulating Materials (AREA)

Abstract

PURPOSE: To obtain a PVC plastisol composition excellent in storage stability at the ordinary temperature, giving PVC coatings having highly hard and insulating properties, and useful for the insulating coatings of high voltage power transmission lines, etc., by using a filling resin, a specific plasticizer, a reactive plasticizer, and a polymerization inhibitor in a specific ratio. CONSTITUTION: This composition comprises (A) 60-75 pts.wt. of a PVC paste resin, (B) 25-40 pts.wt. of a filling resin, (C) 10-30 pts.wt. of dinonyl phthalate or diisodecyl phthalate as a plasticizer, (D) 10-30 pts.wt. of trimethylolpropane trimethacrylate as a reactive plasticizer, and (E) 500-5000ppm of hydroquinone as a polymerization inhibitor.

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、PVCプラスチゾルの
組成物に関しており、具体的にはPVCプラスチゾルの
ディップコーティング組成物に関する。
FIELD OF THE INVENTION This invention relates to PVC plastisol compositions, and more particularly to PVC plastisol dip coating compositions.

【0002】[0002]

【従来の技術】高電圧送電線の地下埋設管には安全性を
確保するために高絶縁被覆が施されているが、直管部は
高絶縁被覆は容易に行なえるがジョイント部は複雑な形
状をしているため絶縁被覆が難しく、粉体樹脂塗料によ
る絶縁被覆とか、PVCプラスチゾルのディップコーテ
ィングが行なわれている。
2. Description of the Related Art Underground pipes for high-voltage transmission lines are provided with a high insulation coating to ensure safety. However, the straight pipe section can be easily coated with a high insulation coating, but the joint section is complicated. Insulation coating is difficult because of its shape, and insulation coating with powder resin paint or dip coating of PVC plastisol is performed.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、前記し
たようなPVCプラスチゾルはPVCペーストレジンを
主体に可塑剤、安定剤、充填剤、顔料等より作られるが
PVCペーストレジン中には界面活性剤が含まれてお
り、一般的なPVCプラスチゾルでは吸湿性が大で電気
絶縁性は低くなり高電圧送電線の地下埋設管の絶縁被覆
材には適さない。本発明はこのような欠点に鑑み、水中
浸漬条件下でも1012Ωcm以上の電気抵抗値を有する
組成物を提供するものである。
However, the PVC plastisol as described above is mainly made of PVC paste resin and is made of a plasticizer, a stabilizer, a filler, a pigment and the like, but the PVC paste resin contains a surfactant. However, general PVC plastisols have high hygroscopicity and low electrical insulation, and are not suitable as insulating coatings for underground pipes of high-voltage transmission lines. In view of such drawbacks, the present invention provides a composition having an electric resistance value of 10 12 Ωcm or more even under immersion in water.

【0004】[0004]

【課題を解決するための手段】本発明は、PVCペース
トレジンを60〜75部、増量剤レジンを25〜40
部、可塑剤としては吸水性の低いDIDPあるいはDI
NPを10〜30部、さらにプラスチゾルの粘度を下げ
加工性(ディッピング性)を良くし加熱キュアーしたも
のの硬度アップのために反応性可塑剤を10〜30部使
用し、次に反応性可塑剤の常温での反応を抑制するため
に重合禁止剤と分解温度の比較的高い重合開始剤を用い
る。
According to the present invention, 60 to 75 parts of PVC paste resin and 25 to 40 parts of extender resin are used.
Part, DIDP or DI with low water absorption as a plasticizer
10 to 30 parts by weight of NP, 10 to 30 parts by weight of the reactive plasticizer to further improve the hardness of the cured product by further lowering the viscosity of the plastisol and improving the processability (dipping property), and then the reactive plasticizer In order to suppress the reaction at room temperature, a polymerization inhibitor and a polymerization initiator having a relatively high decomposition temperature are used.

【0005】[0005]

【作用】一般に反応性可塑剤を重合させるためにパーオ
キサイド重合開始剤を加えるが、パーオキサイドは常温
でも徐々に分解してラジカルを生成し、反応性可塑剤を
重合させる傾向がある。すなわち、常温貯蔵中に反応が
進み粘度が上昇しゾルがゲル化してディップコーティン
グに使えなくなる欠点がある。
In general, a peroxide polymerization initiator is added to polymerize the reactive plasticizer, but the peroxide tends to gradually decompose even at room temperature to generate radicals and polymerize the reactive plasticizer. That is, there is a drawback that the reaction proceeds during normal temperature storage, the viscosity increases, and the sol gels and cannot be used for dip coating.

【0006】本発明は特にこの点の改良を目的として常
温でのパーオキサイドの分解を遅らせるために分解温度
の比較的高いパーオキサイドを使用し、常温でパーオキ
サイドが分解してラジカルが発生してもこのラジカルを
キャッチする重合禁止剤を500〜5000ppm反応
性可塑剤に加えることにより常温での反応を抑制し、常
温で6〜12ヶ月の長期に亘ってプラスチゾルの粘度上
昇を起こさず、かつディップコーティング作業中の粘度
上昇も極めて低いプラスチゾルを得ることができ、かつ
このゾルを200℃で加熱キュアーすると速やかに溶融
物となりパーオキサイドが分解してラジカルが発生し反
応性可塑剤を重合させて高硬度で高強度高絶縁性のPV
C被覆となる。
In order to improve this point, the present invention uses a peroxide having a relatively high decomposition temperature in order to delay the decomposition of peroxide at room temperature, and the peroxide is decomposed at room temperature to generate radicals. Also, by adding a polymerization inhibitor that catches this radical to the reactive plasticizer of 500 to 5000 ppm, the reaction at room temperature is suppressed, the viscosity of plastisol does not rise for a long period of 6 to 12 months at room temperature, and the dip It is possible to obtain a plastisol with a very low increase in viscosity during coating work, and when this sol is heated and cured at 200 ° C, it quickly becomes a melt and peroxide decomposes to generate radicals, which polymerizes the reactive plasticizer to a high degree. PV with hardness and high strength and insulation
It becomes C coating.

【0007】[0007]

【実施例】以下に本発明の実施例を示す。 PVCペーストレジン 70部 増量材レジン 30部 可塑剤DIDP 30部 反応性可塑剤TMPT 15部 (重合禁止剤2000ppm入り) 熱安定剤 2.5部 キレーター1292 0.5部 重合開始剤 0.2部 トナー 1.0部 上記ゾルの粘度3000cps. 上記ゾルを200℃で12分ギャーオーブン中で加熱す
ると、 硬度 ジョアA 93° 伸び 240% 引っ張り強さ 220kg/cm2 電気抵抗 Dry 1014Ωcm以上 水中5日浸漬 1012Ωcm以上 の高硬度、高絶縁性でありながら、常温での貯蔵安定性
が良く加熱の際は速やかに溶融反応する組成物が得られ
た。
Examples of the present invention will be described below. PVC paste resin 70 parts Extender resin 30 parts Plasticizer DIDP 30 parts Reactive plasticizer TMPT 15 parts (Polymerization inhibitor 2000 ppm is included) Thermal stabilizer 2.5 parts Chelator 1292 0.5 parts Polymerization initiator 0.2 parts Toner 1.0 part Viscosity of the above sol 3000 cps. When the above sol is heated at 200 ° C. for 12 minutes in a gear oven, hardness Joa A 93 ° elongation 240% tensile strength 220 kg / cm 2 electrical resistance Dry 10 14 Ωcm or more 5 days immersion in water 10 12 Ωcm or more high hardness, high A composition was obtained that was insulating but had good storage stability at room temperature and rapidly melted when heated.

【0008】[0008]

【発明の効果】本発明によると、水中浸漬条件下でも1
12Ωcm以上の電気抵抗値を有する組成物となる。ま
た、常温で6〜12ヶ月の長期に亘ってプラスチゾルの
粘度上昇を起こさず、かつディップコーティング作業中
の粘度上昇も極めて低いプラスチゾルを得ることがで
き、かつこのゾルを200℃で加熱キュアーすると速や
かに溶融物となりパーオキサイドが分解してラジカルが
発生し反応性可塑剤を重合させて高硬度で高強度高絶縁
性のPVC被覆となる。
EFFECTS OF THE INVENTION According to the present invention, 1
The composition has an electric resistance value of 0 12 Ωcm or more. Further, it is possible to obtain a plastisol that does not increase in viscosity of plastisol for a long period of 6 to 12 months at room temperature and has an extremely small increase in viscosity during dip coating work. Then, it becomes a melt and peroxide decomposes to generate radicals to polymerize the reactive plasticizer to form a PVC coating with high hardness, high strength and high insulation.

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01B 3/44 P Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI Technical display area H01B 3/44 P

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 PVCプラスチゾル組成物において、増
量剤レジンを25〜40phr使用し、可塑剤としてジ
ノニル・フタレートあるいはジイソデシル・フタレート
を10〜30phr用いると共に反応性可塑剤としてト
リメタクリル酸トリメチロールプロパンを10〜30p
hr用い、さらに重合禁止剤としてハイドロキノンを5
00〜5000ppm用いたことを特徴とするPVCプ
ラスチゾル組成物。
1. In a PVC plastisol composition, 25 to 40 phr of an extender resin is used, 10 to 30 phr of dinonyl phthalate or diisodecyl phthalate is used as a plasticizer, and 10 parts of trimethylolpropane trimethacrylate is used as a reactive plasticizer. ~ 30p
and used hydroquinone as a polymerization inhibitor.
A PVC plastisol composition, which is used in an amount of from 0.00 to 5000 ppm.
JP28914494A 1994-10-28 1994-10-28 Pvc plastisol composition Pending JPH08127694A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28914494A JPH08127694A (en) 1994-10-28 1994-10-28 Pvc plastisol composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28914494A JPH08127694A (en) 1994-10-28 1994-10-28 Pvc plastisol composition

Publications (1)

Publication Number Publication Date
JPH08127694A true JPH08127694A (en) 1996-05-21

Family

ID=17739332

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28914494A Pending JPH08127694A (en) 1994-10-28 1994-10-28 Pvc plastisol composition

Country Status (1)

Country Link
JP (1) JPH08127694A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100426229B1 (en) * 2001-01-05 2004-04-08 주식회사 엘지화학 Trimethyl olpropane ester based plasticizer composition for polyvinyl chloride resin
KR100456546B1 (en) * 2001-12-11 2004-11-10 현대자동차주식회사 Composition of nontoxic polyvinyl chloride resin compound
JP2008303252A (en) * 2007-06-05 2008-12-18 Daihachi Chemical Industry Co Ltd Stabilized composition
CN111777831A (en) * 2020-08-21 2020-10-16 柳州紫荆技术转移中心有限公司 Graphene modified PVC plastisol for automobile chassis and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100426229B1 (en) * 2001-01-05 2004-04-08 주식회사 엘지화학 Trimethyl olpropane ester based plasticizer composition for polyvinyl chloride resin
KR100456546B1 (en) * 2001-12-11 2004-11-10 현대자동차주식회사 Composition of nontoxic polyvinyl chloride resin compound
JP2008303252A (en) * 2007-06-05 2008-12-18 Daihachi Chemical Industry Co Ltd Stabilized composition
CN111777831A (en) * 2020-08-21 2020-10-16 柳州紫荆技术转移中心有限公司 Graphene modified PVC plastisol for automobile chassis and preparation method thereof

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