JPH01304106A - Curing agent for putty composition - Google Patents

Curing agent for putty composition

Info

Publication number
JPH01304106A
JPH01304106A JP13435688A JP13435688A JPH01304106A JP H01304106 A JPH01304106 A JP H01304106A JP 13435688 A JP13435688 A JP 13435688A JP 13435688 A JP13435688 A JP 13435688A JP H01304106 A JPH01304106 A JP H01304106A
Authority
JP
Japan
Prior art keywords
container
curing agent
peroxide
partition wall
acyl
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
JP13435688A
Other languages
Japanese (ja)
Other versions
JPH0629400B2 (en
Inventor
Akira Yamanaka
明 山中
Hiromoto Takagi
高木 弘基
Susumu Kitagawa
進 北川
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.)
Resonac Corp
Original Assignee
Hitachi Kasei Polymer 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 Hitachi Kasei Polymer Co Ltd filed Critical Hitachi Kasei Polymer Co Ltd
Priority to JP63134356A priority Critical patent/JPH0629400B2/en
Publication of JPH01304106A publication Critical patent/JPH01304106A/en
Publication of JPH0629400B2 publication Critical patent/JPH0629400B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Sealing Material Composition (AREA)
  • Polymerization Catalysts (AREA)
  • Paints Or Removers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

PURPOSE:To prepare a good curing agent having an extremely high workability by filling a ketone peroxide and a acyl peroxide divided by a partition wall in a container and extruding these two liq. from this container and mixing them when they are used. CONSTITUTION:A ketone peroxide 2 and an acyl peroxide 2' are filled in a container 1 divided by a partition wall 3 and, when they are used, these two liq. 2 and 2' are extruded from the container 1 by, e.g., pushing a pushing bar 5 against plungers 4 and mixed together. The ketone peroxide and the acyl peroxide have each a defect as a curing agent, but when they are simultaneously used, only their merits are exhibited. However, when they are mixed together, the lifecycle as a curing agent becomes short and it is therefore necessary to keep them at a cool and dark place. It is possible to make a good curing agent having an extremely high workability by using a container having a partition wall.

Description

【発明の詳細な説明】 (発明の属する分野) 本発明はパテ組成物を実際に使用する場合に極めて作業
性の良好な硬化剤を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field to which the invention pertains) The present invention provides a curing agent that has extremely good workability when a putty composition is actually used.

(従来技術の説明) 従来パテ組成物は、不飽和ポリエステルに充てん剤を混
合した主剤と過酸化物をペースト化した硬化剤とから構
成されている。
(Description of Prior Art) Conventional putty compositions are composed of a base material made of unsaturated polyester mixed with a filler and a hardening agent made of peroxide paste.

過酸化物として、メチルエチルケトンパーオキサイド、
メチルイソブチルケトンパーオキサイド、シクロヘキサ
ノンパーオキサイド、メチルシクロヘキサノンパーオキ
サイドなどのケトン系パーオキサイドと、ベンゾイルパ
ーオキサイドのようなアシル系パーオキサイドが汎用で
ある。レドックス触媒を用いて常温硬化させるため、ケ
トン系パーオキサイドは、ナフテン酸コバルトなどコバ
ルト塩を触媒とし、アシル系パーオキサイドは、ジメチ
ルアニリンなどアミン系化合物を触媒としている。この
組合せからパテ組成物としての特性が表われ、ベンゾイ
ルパーオキサイドを用いると被着体に対する接着性が良
いが触媒のアミンによる塗装面の汚染が現われる。また
、パテの硬化時、空気との接着面に粘着性が残りなかな
かタックフリーにならない、ケトン系パーオキサイドを
用いると被着体に対する接着性は、アシル系に比べてや
1劣るが塗装面の汚染は、はとんどない、また、硬化後
のパラ表面のタックフリーはアシル系に比較して速いが
、反応は緩慢であるため硬度の立上りは遅い0本発明は
このような従来の問題点を解消し、併せて著しく作業性
を改善した良好な硬化剤を提供するものである。
As a peroxide, methyl ethyl ketone peroxide,
Ketone peroxides such as methyl isobutyl ketone peroxide, cyclohexanone peroxide, and methyl cyclohexanone peroxide, and acyl peroxides such as benzoyl peroxide are commonly used. To cure at room temperature using a redox catalyst, ketone peroxides use a cobalt salt such as cobalt naphthenate as a catalyst, and acyl peroxides use an amine compound such as dimethylaniline as a catalyst. This combination exhibits properties as a putty composition, and when benzoyl peroxide is used, adhesion to the adherend is good, but staining of the painted surface due to the catalytic amine occurs. In addition, when the putty hardens, tack remains on the surface that adheres to the air, making it difficult to become tack-free.When using a ketone-based peroxide, the adhesion to the adherend is slightly inferior to that of an acyl-based putty, but the adhesiveness remains on the painted surface. Contamination is rare, and the tack-free surface of the para surface after curing is faster than that of acyl-based materials, but the reaction is slow, so the rise in hardness is slow.The present invention solves these conventional problems. The object of the present invention is to provide a good curing agent which solves the above problems and also significantly improves workability.

(発明の構成) 本発明は一つの容器に隔壁を界してケトン系パーオキサ
イドとアシル系パーオキサイドとを充てんさせ、使用の
際に当該二液を当該容器から吐出し混合してなることを
特徴とするパテ組成物用硬化剤に関する。
(Structure of the Invention) The present invention is characterized in that a single container is filled with a ketone peroxide and an acyl peroxide with a partition wall between them, and when used, the two liquids are discharged from the container and mixed. The present invention relates to a characteristic curing agent for putty compositions.

前述した通すケトン系パーオキサイドとアシル系パーオ
キサイドはそれぞれ硬化剤としての欠点を有しているが
、これを同時に使用する方法を追求したところ1両者の
長所だけが呪われ、従来の自動車補修パテの特性が大幅
に改善されることを見い出した。ところがケトン系パー
オキサイドとアシル系パーオキサイドを混合すると硬化
剤のライフサイクルが短くなり、商品化するには冷暗所
保管が必要となる。
The above-mentioned penetrating ketone peroxide and acyl peroxide each have their drawbacks as hardeners, but when we pursued a method of using them simultaneously, we found that only the advantages of both were cursed, and that the conventional automotive repair putty It was found that the properties of the material were significantly improved. However, when a ketone peroxide and an acyl peroxide are mixed, the life cycle of the curing agent is shortened, and storage in a cool, dark place is required for commercialization.

又、硬化剤を別々の容器に入れて使えば従来1回で済む
作業が2回となり作業が増加するだけでなく硬化剤量の
計量も従来の半分となるため計量精度の低下でパテ組成
物の品質にも問題が発生する。
In addition, if the hardening agent is placed in separate containers, it will require two steps instead of one, which not only increases the amount of work required, but also reduces the amount of hardening agent measured by half compared to the conventional method, resulting in a decrease in measurement accuracy and a reduction in the quality of the putty composition. There are also problems with the quality of

本発明はこのような問題に対して隔壁を有する容器を使
用することにより解決し、極めて作業性の高い良好な硬
化剤を作ることに成功した。
The present invention solved this problem by using a container with partition walls, and succeeded in producing a good curing agent with extremely high workability.

隔壁のある容器から同時にそれぞれを取出す方法として
ピストン方式と絞出方式が考えられる。
A piston method and a squeezing method are conceivable as methods for simultaneously taking out each substance from a container with a partition wall.

ピストン方式としては、容器には変形しにくい材質でポ
リエチレンやポリプロプレンの成形品がある。また絞出
方式としては容器は変形し易い材質でポリエチレンやポ
リプロピレンのフィルム状のものがある。
For the piston type, the container is made of polyethylene or polypropylene, which is a material that does not easily deform. In addition, in the squeezing method, the container is made of a film-like material such as polyethylene or polypropylene, which is easily deformable.

実施例について説明すれば、1は容器本体(ネジ付キャ
ップ付)である、押出棒5をプランジャー4に押し当て
ることにより1の反対側の先端から隔壁3を界して硬化
剤2.2′が出てくる。
To explain the embodiment, 1 is a container body (with a screw cap), and by pressing an extrusion rod 5 against a plunger 4, a curing agent 2.2 is introduced from the opposite tip of 1 across a partition wall 3. ' will appear.

又、フィルム状容器の場合、使用時に、フィルムヒート
シール部6の切り込み7で容器の口を開き、プラスチッ
ク治具8,9でシールされた端部より巻き取りハンドル
10を回転させてフィルムを絞りながら押出口より硬化
剤を吐出し混合してパテ組成物の硬化剤として使用する
In the case of a film-like container, when in use, the mouth of the container is opened at the notch 7 of the film heat-sealing section 6, and the film is squeezed by rotating the winding handle 10 from the end sealed with the plastic jigs 8 and 9. At the same time, the curing agent is discharged from the extrusion port, mixed, and used as a curing agent for the putty composition.

(実施例および比較例の説明) 次に実施例および比較例を挙げて本発明を具体的に説明
する。
(Description of Examples and Comparative Examples) Next, the present invention will be specifically described with reference to Examples and Comparative Examples.

実施例1. 不飽和ポリエステル樹脂ポリセット171
4B (日立化成工業KK製)40重量パーセントに輸
入タルク TALC8P(日本タルクKK製)30重量
パーセント超微粒子炭酸カルシウムMS−100(日東
粉化工業KK製)30重量パーセント及び硬化促進剤C
T−13(日立化成工業KK製)5重量パーセントを均
一になるまで混合し、主剤とした。このパテ組成物の主
剤100重量パーセントに対して図1に示す容器を用い
て、ベンシルパーオキサイド ナイバーBO(日本油脂
KK製)とケトンパーオキサイド パーへキサD(日本
油脂KK製)とを各1重量パーセント混合し、特性を調
べた。その結果を表1に示す。
Example 1. Unsaturated polyester resin Polyset 171
4B (manufactured by Hitachi Chemical KK) 40% by weight, imported talc TALC8P (manufactured by Nippon Talc KK) 30% by weight ultrafine particle calcium carbonate MS-100 (manufactured by Nitto Funka Kogyo KK) 30% by weight and hardening accelerator C
5% by weight of T-13 (manufactured by Hitachi Chemical Co., Ltd. KK) was mixed until uniform to form a main ingredient. Using the container shown in FIG. 1, one portion each of benzyl peroxide Nyver BO (manufactured by NOF KK) and ketone peroxide Perhexa D (manufactured by NOF KK) was added to 100% by weight of the main ingredient of this putty composition. The weight percentages were mixed and the properties were investigated. The results are shown in Table 1.

比較例1. 実施例1で作成した主剤1oO重景パーセ
ントに対してナイパーBOを2重量パーセント混合し、
特性を調べた。その結果を表1に示す。
Comparative example 1. 2 weight percent of Niper BO was mixed with 100 weight percent of the base material prepared in Example 1,
We investigated the characteristics. The results are shown in Table 1.

比較例2. 実施例1で作成した主剤100重量パーセ
ントに対してパーへキサDを2重量パーセント混合し、
特性を調べた。その結果を表1に示す。
Comparative example 2. 2% by weight of Perhexa D was mixed with 100% by weight of the base material prepared in Example 1,
We investigated the characteristics. The results are shown in Table 1.

比較例3. 実施例1で作成した主剤100重要パーセ
ントに対してナイパーBOとパーへキサDとを等景況合
したポリエチレンチューブ入り硬化剤2重量パーセント
を混合し、特性を調べた。
Comparative example 3. To 100 weight percent of the base resin prepared in Example 1, 2 weight percent of a hardening agent in a polyethylene tube containing equal proportions of Niper BO and Perhexa D was mixed and the properties were investigated.

その結果を表1に示す。The results are shown in Table 1.

く備考〉 (1)接着性の評価: 0:パテ層凝集破壊、Δ:混合
破壊、×:界面はく離(2)耐湿熱性の評価: 接着°
性試験片を50℃X95%RHに10時間放置し、接着
性と同様の評価をした。
Notes> (1) Evaluation of adhesiveness: 0: Cohesive failure of putty layer, Δ: Mixed failure, ×: Interfacial peeling (2) Evaluation of heat and humidity resistance: Adhesion °
The test pieces were left at 50° C. and 95% RH for 10 hours, and evaluated in the same way as for adhesiveness.

(3)乾燥性の評価: 20℃でパテを硬化させ、硬化
後20分経過した時の表面指触タックを調べた。
(3) Evaluation of drying properties: The putty was cured at 20°C, and the surface tack to the touch was examined 20 minutes after curing.

0:タッフリーΔ:少しタック有り ×:タック有る(
本発明の効果) 以上のように1本発明のパテ組成物用硬化剤により本件
に関する従来技術の間厘点が解決され、極めて良好なパ
テ組成物が提供されることになる。
0: Tough free Δ: Slight tack ×: Tack (
Effects of the present invention) As described above, the curing agent for putty compositions of the present invention solves the shortcomings of the prior art related to this problem, and provides an extremely good putty composition.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の断面図であり第2図は本発明の平面図
であり第3図は本発明の正面図である。 1・・・容器本体(ネジ付キャップ付)2・・・ケトン
系パーオキサイド又はアシル系パーオキサイド2′ ・
・ 3・・・隔壁 4・・・プランジャー 5・・・押出棒 6・・・フィルムヒートシール部 7・・・切り込み 8・・・フィルム端部を閉じるプラスチック治具(雄型
)9・・・フィルム端部を閉じるプラスチック治具(雌
型)10・・・巻き取りハンドル 以  上
FIG. 1 is a sectional view of the invention, FIG. 2 is a plan view of the invention, and FIG. 3 is a front view of the invention. 1... Container body (with screw cap) 2... Ketone peroxide or acyl peroxide 2' ・
・ 3... Partition wall 4... Plunger 5... Extrusion rod 6... Film heat sealing part 7... Notch 8... Plastic jig (male type) for closing the film end 9...・Plastic jig (female type) for closing the film end 10... Winding handle or more

Claims (1)

【特許請求の範囲】[Claims] 一つの容器に隔壁を界してケトン系パーオキサイドとア
シル系パーオキサイドを充てんさせ、使用の際に当該二
液を当該容器から吐出し混合してなることを特徴とする
パテ組成物用硬化剤
A hardening agent for a putty composition, characterized in that a container is filled with a ketone peroxide and an acyl peroxide with a partition wall between them, and when used, the two liquids are discharged from the container and mixed.
JP63134356A 1988-06-02 1988-06-02 Curing agent for putty composition Expired - Fee Related JPH0629400B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63134356A JPH0629400B2 (en) 1988-06-02 1988-06-02 Curing agent for putty composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63134356A JPH0629400B2 (en) 1988-06-02 1988-06-02 Curing agent for putty composition

Publications (2)

Publication Number Publication Date
JPH01304106A true JPH01304106A (en) 1989-12-07
JPH0629400B2 JPH0629400B2 (en) 1994-04-20

Family

ID=15126455

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63134356A Expired - Fee Related JPH0629400B2 (en) 1988-06-02 1988-06-02 Curing agent for putty composition

Country Status (1)

Country Link
JP (1) JPH0629400B2 (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5022893A (en) * 1973-06-28 1975-03-11
JPS51134741A (en) * 1975-05-06 1976-11-22 Syntex Inc Method of producing betaastage unsaturated polyester resin
JPS5740507A (en) * 1980-08-25 1982-03-06 Kayaku Nuurii Kk Peroxide mixture composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5022893A (en) * 1973-06-28 1975-03-11
JPS51134741A (en) * 1975-05-06 1976-11-22 Syntex Inc Method of producing betaastage unsaturated polyester resin
JPS5740507A (en) * 1980-08-25 1982-03-06 Kayaku Nuurii Kk Peroxide mixture composition

Also Published As

Publication number Publication date
JPH0629400B2 (en) 1994-04-20

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