JPS6134104A - Organic impregnant having good stability for metal - Google Patents

Organic impregnant having good stability for metal

Info

Publication number
JPS6134104A
JPS6134104A JP15637184A JP15637184A JPS6134104A JP S6134104 A JPS6134104 A JP S6134104A JP 15637184 A JP15637184 A JP 15637184A JP 15637184 A JP15637184 A JP 15637184A JP S6134104 A JPS6134104 A JP S6134104A
Authority
JP
Japan
Prior art keywords
polymn
impregnant
initiator
meth
impregnation
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
JP15637184A
Other languages
Japanese (ja)
Inventor
Kosaku Shimada
島田 耕作
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.)
SEVEN CHEM KK
Original Assignee
SEVEN CHEM KK
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 SEVEN CHEM KK filed Critical SEVEN CHEM KK
Priority to JP15637184A priority Critical patent/JPS6134104A/en
Publication of JPS6134104A publication Critical patent/JPS6134104A/en
Pending legal-status Critical Current

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  • Powder Metallurgy (AREA)

Abstract

PURPOSE:To provide an impregnant having an extended stable period in a pot life by adding a metallic chelate compd. to an org. impregnant consisting of a (meth)acrylate, polymn. initiator and polymn. inhibitor. CONSTITUTION:This impregnant for metal consists of the acrylate or methacrylate monomer, polymn. initiator, polym. inhibitor and the metallic chelate compd. as a stabilizer. The characteristic of the impregnant after impregnation is exactly the same as the characteristic of the basic compsn. consisting of the (meth)acrylate monomer and polymn. initiator and polymn. inhibor and only the stable perod in the pot life is extended. The metallic chelate compd. which is the stabilizer refers to ethylenediaminetetraacetic acid, N-hydroxyethyl ethylenediamine N, N', N' trictid acid, etc. which produce a water soluble chelate compd. by binding with metallic ions.

Description

【発明の詳細な説明】 本発明は、安定性の改良された金属用有機含浸剤に関す
るものである。金属の含浸剤は既に知られているように
、嫌気硬化性を示すラジカル重合性のアクリル酸エステ
ルおよび/またはメタクリル酸エステル単量体と重合開
始剤、重合抑制剤との混合物であり、この含浸剤は鋳造
あるいは粉末冶金等で生じる欠陥穴を埋め、部品として
の気密性を高めることが出来るため使用されている。従
来、鋳物に対する含浸処理は気密性保持が必要である鋳
物部品の救済手段として、ケイ酸ソーダが主成分である
含浸剤を使用しているが、部品メーカーの品質要求が高
くなるに従って、ケイ酸ソーダ系含浸剤で処理した鋳物
部品の信頼性は低下している。その主な理由は、ケイ酸
ソーダの固形分と硬化機構に原因があり、処理後の機械
加工や塗装・組立て工程において、未硬化の含浸剤が流
れ出る等のトラブルが発生しやすことにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to organic impregnating agents for metals with improved stability. As is already known, a metal impregnating agent is a mixture of a radically polymerizable acrylic ester and/or methacrylic ester monomer that exhibits anaerobic curing properties, a polymerization initiator, and a polymerization inhibitor; The agent is used because it can fill in defects caused by casting or powder metallurgy, etc., and improve the airtightness of parts. Conventionally, impregnation treatment for castings has used an impregnating agent whose main ingredient is sodium silicate as a means of saving cast parts that need to maintain airtightness, but as the quality requirements of parts manufacturers have become higher, Reliability of cast parts treated with soda-based impregnation agents is reduced. The main reason for this is the solid content and curing mechanism of sodium silicate, which tends to cause problems such as uncured impregnating agent flowing out during machining, painting, and assembly processes after treatment.

公知の有機含浸剤は、この様なケイ酸ソーダ系含浸剤の
欠点を解決出来る次の特徴があり、処理後の性能は安定
している。
Known organic impregnating agents have the following characteristics that can overcome the drawbacks of such sodium silicate-based impregnating agents, and their performance after treatment is stable.

■、ケイ酸ソーダ系含浸剤に比べて、粘度・表面張力が
小さいので、良く浸透する。
■ Compared to sodium silicate impregnation agents, it has a lower viscosity and surface tension, so it penetrates better.

■、ケイ酸ソーダ系含浸剤に比べて、液は100*の固
化物になる。
(2) Compared to a sodium silicate impregnation agent, the liquid becomes a solidified product of 100*.

■、硬化(重合)温度が定まっているので、含浸後の経
時変化が非常に小さい。
(2) Since the curing (polymerization) temperature is fixed, the change over time after impregnation is very small.

しかしながら、含浸処理時の取り扱いはケイ酸ソーダ系
含浸剤に比べて、保冷した状態でないと長期間の使用に
耐えないという重要な欠点がある。
However, compared to the sodium silicate impregnating agent, it has an important drawback in handling during impregnation treatment, in that it cannot withstand long-term use unless it is kept cold.

通常、公知の有機含浸剤を使用するには、材質はステン
レスで、冷却可能な装置が必要である。
Generally, the use of known organic impregnating agents requires stainless steel and cooling equipment.

又、含浸処理中に周辺温度が高いと鋳物表面でのゲル化
を生じ、洗浄が回能になり外観不良になるなどの欠点が
ある。
In addition, if the ambient temperature is high during the impregnation process, gelation occurs on the surface of the casting, making cleaning difficult and resulting in poor appearance.

本発明者は前述の欠点を改良すべく研究を重ねた結果、
ラジカル重合可能な(メタ)アクリル酸エステル単量体
と重合開始剤・重合抑制剤および金属キレート化合物か
らなる組成物が本発明の目的に最適な有機含浸剤となり
得ることを見出した。
As a result of repeated research to improve the above-mentioned drawbacks, the present inventor found that
It has been found that a composition comprising a radically polymerizable (meth)acrylic acid ester monomer, a polymerization initiator/polymerization inhibitor, and a metal chelate compound can serve as an optimal organic impregnating agent for the purpose of the present invention.

本発明に係る有機含浸剤では、含浸後の特性は(メタ)
アクリル酸エステル単量体と重合開始剤・重合抑制剤か
らなる基本組成物のそれと比較してまったく低下するこ
とがなく、可使時の安定期間のみ増大する。
In the organic impregnating agent according to the present invention, the properties after impregnation are (meta)
Compared to the basic composition consisting of an acrylic acid ester monomer and a polymerization initiator/polymerization inhibitor, there is no deterioration at all, and only the stability period during use is increased.

つぎに本発明の含浸剤に使用するに最適な単量体は、(
メタ)アクリル酸エステルであり、っぎのごときものを
例示することが出来る。
Next, the monomer most suitable for use in the impregnating agent of the present invention is (
It is a meth)acrylic acid ester, and examples include meth)acrylic acid esters.

(メタ)アクリル酸2−とドロキシエチル、(メタ)ア
クリル12−ヒドロキシプロピル、(メタ)アクリルI
l!1゜4ブタンジオール、(メタ)アクリル8!1.
6ヘキサンジオール、メタクリル酸グリシジル、メタク
リル+1!2−エチルヘキシル、メタクリル酸アルキル
、メタクリル酸トリデシル、メタクリル酸シクロヘキシ
ル、メタクリル酸ラウリル、ジメタクリル酸ポリエチレ
ングリコール、ジメタクリル醒ポリ10ピレングリコー
ル、ジメタクリル酸トリエヂレングリコール、ジメタク
リル酸ジエチレングリコール、ジメタクリル酸ネオペン
チルグリコール、ジメタクリルl!16ヘキサンジオー
ル等である。
(meth)acrylic acid 2- and droxyethyl, (meth)acrylic 12-hydroxypropyl, (meth)acrylic I
l! 1゜4butanediol, (meth)acrylic 8!1.
6-hexanediol, glycidyl methacrylate, methacrylic + 1!2-ethylhexyl, alkyl methacrylate, tridecyl methacrylate, cyclohexyl methacrylate, lauryl methacrylate, polyethylene glycol dimethacrylate, dimethacrylate-strength poly-10-pyrene glycol, triedyl dimethacrylate Ren glycol, diethylene glycol dimethacrylate, neopentyl glycol dimethacrylate, dimethacrylate l! 16 hexanediol and the like.

重合抑制剤は0−ニトロソフェノール、ハイドロキノン
、4−メトキシフェノール、メトキノン等である。
Polymerization inhibitors include 0-nitrosophenol, hydroquinone, 4-methoxyphenol, and methoquinone.

重合開始剤はパーオキシエステル、ハイドロパーオキサ
イド、ジアシルパーオキサイド等である。
Polymerization initiators include peroxy esters, hydroperoxides, diacyl peroxides, and the like.

本発明でいう安定剤である金属キレート化合物とは、金
属イオンと結合して水溶性キレート化合物を作るEDT
A (エチレンジアミン四酢酸)、HEEDTA (N
−ヒト0キシエチルエチレンジアミンN、N′、N−三
酢酸)、DTPA(ジエチレントリアミン万酢酸)、T
HPED (N、NN−、N−、テトラキス2−ヒドロ
キシプロピルエチレンジアミン)、EDDA(エチレン
ジアミンN、N”二酢m’) 、HEDPA (1−ヒ
ドロキシエチリデン1−1.二燐!lj) 、TTHA
 (、t−リエチレンテトラミンN、N−,N−、N=
、N−六酢酸)である。
The metal chelate compound as a stabilizer in the present invention refers to EDT, which combines with metal ions to form a water-soluble chelate compound.
A (ethylenediaminetetraacetic acid), HEEDTA (N
-human 0xyethylethylenediamine N,N',N-triacetic acid), DTPA (diethylenetriamine panacetic acid), T
HPED (N, NN-, N-, tetrakis 2-hydroxypropylethylenediamine), EDDA (ethylenediamine N, N" diacetate m'), HEDPA (1-hydroxyethylidene 1-1. diphosphorus! lj), TTHA
(, t-lyethylenetetramine N, N-, N-, N=
, N-hexaacetic acid).

次に本発明の詳細をさらに具体的に示すために、実施例
をあげる。
Next, Examples will be given to show the details of the present invention more specifically.

尚、含浸効果、亜鉛・銅に対する安定性、光・温度に対
する安定性は次の方法によって測定した。
The impregnation effect, stability against zinc and copper, and stability against light and temperature were measured by the following methods.

含浸効果: 比重6.2のリング状鉄焼結体を各5個づつ浸漬・真空
法で含浸し、90度Cの熱水に15分間浸漬硬化機気密
試験(圧力5に9/d)をおこなう。
Impregnation effect: Five ring-shaped iron sintered bodies with a specific gravity of 6.2 were impregnated using the immersion/vacuum method, and were immersed in hot water at 90 degrees Celsius for 15 minutes to undergo a hardening airtightness test (pressure 5 to 9/d). Let's do it.

亜鉛・銅に対する安定性: 5dの無色透明なガラス瓶に含浸剤を2d入れ、亜鉛と
銅の棒を浸し、25度Gの雰囲気でゲル化期間を測定し
た。
Stability against zinc and copper: 2 d of impregnating agent was placed in a 5 d colorless and transparent glass bottle, zinc and copper rods were immersed, and the gelation period was measured in an atmosphere of 25 degrees G.

光・温度に対する安定性: 300dの無色透明なガラス瓶に含浸剤を300d入れ
、日当り(気温23〜35度C)に置いて、ゲル化期間
を測定した。
Stability against light and temperature: 300 d of impregnating agent was placed in a 300 d colorless and transparent glass bottle, placed in the sun (temperature 23 to 35 degrees Celsius), and the gelation period was measured.

実施例 メタクリル酸エステルの単量体の一種である2−ヒドロ
キシエチルメタクリレート800部、ジメタクリル酸ポ
リプロピレングリコール100部、グリシジルメタクリ
レート100部の混合物を用い、これに次の成分を添加
調合してl+81含浸剤を得た。
Example Using a mixture of 800 parts of 2-hydroxyethyl methacrylate, which is a type of monomer of methacrylic acid ester, 100 parts of polypropylene glycol dimethacrylate, and 100 parts of glycidyl methacrylate, the following components were added and prepared for l+81 impregnation. obtained the drug.

t−7チルバーオキシ2−エヂルヘキリネート(重合開
始剤)   20部 ハイドロキノン・モノメチルエーテル (重合抑υ1剤)    2部 この含浸剤を10等分し、N(11〜6の含浸剤に本発
明の範囲内にある金属キレート化合物を、N。
20 parts of t-7 tilveroxy 2-edylhexylnate (polymerization initiator) 2 parts of hydroquinone monomethyl ether (1 polymerization inhibitor) The metal chelate compound within the range of N.

1〜3にはTHPED、Nf14〜6にはHEDPAを
添加し、比較として、Nα7にはハイドロキノン、順8
にはO号ンルベント、llQ9にはβ−プフトールアル
デヒドを添加、順10は無添加とした。
THPED was added to 1 to 3, HEDPA was added to Nf14 to 6, and for comparison, hydroquinone was added to Nα7, and HEDPA was added to Nf14 to 6.
No. 0 nlubento was added, β-puftholaldehyde was added to 11Q9, and no addition was made to No. 10.

それぞれにつき亜鉛・銅に対する安定性、光・温度に対
する安定性、含浸効果を測定した。その結果を表−1に
示す。
For each, the stability against zinc and copper, the stability against light and temperature, and the impregnation effect were measured. The results are shown in Table-1.

表−1 以上の幕に、本発明品は金属に対しても、光・板 温度に対しても、安定な有機含浸剤である。Table-1 Based on the above, the product of the present invention can be applied to metals as well as light and plates. It is an organic impregnating agent that is stable even with respect to temperature.

Claims (1)

【特許請求の範囲】[Claims] アクリル酸エステルおよび/またはメタクリル酸エステ
ル単量体、重合開始剤、重合抑制剤、および安定剤とし
ての金属キレート化合物からなる金属用含浸剤
Impregnating agent for metals consisting of an acrylic ester and/or methacrylic ester monomer, a polymerization initiator, a polymerization inhibitor, and a metal chelate compound as a stabilizer
JP15637184A 1984-07-26 1984-07-26 Organic impregnant having good stability for metal Pending JPS6134104A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15637184A JPS6134104A (en) 1984-07-26 1984-07-26 Organic impregnant having good stability for metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15637184A JPS6134104A (en) 1984-07-26 1984-07-26 Organic impregnant having good stability for metal

Publications (1)

Publication Number Publication Date
JPS6134104A true JPS6134104A (en) 1986-02-18

Family

ID=15626289

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15637184A Pending JPS6134104A (en) 1984-07-26 1984-07-26 Organic impregnant having good stability for metal

Country Status (1)

Country Link
JP (1) JPS6134104A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0221609U (en) * 1988-07-29 1990-02-14

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0221609U (en) * 1988-07-29 1990-02-14

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