JPH05278041A - Polyurethane remover - Google Patents

Polyurethane remover

Info

Publication number
JPH05278041A
JPH05278041A JP10554892A JP10554892A JPH05278041A JP H05278041 A JPH05278041 A JP H05278041A JP 10554892 A JP10554892 A JP 10554892A JP 10554892 A JP10554892 A JP 10554892A JP H05278041 A JPH05278041 A JP H05278041A
Authority
JP
Japan
Prior art keywords
polyurethane
remover
weight
parts
sodium hydroxide
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
JP10554892A
Other languages
Japanese (ja)
Other versions
JP2892213B2 (en
Inventor
Kuniyasu Yamazaki
邦康 山崎
Shigeaki Hirose
恵朗 広瀬
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.)
Hoya Corp
Original Assignee
Hoya 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 Hoya Corp filed Critical Hoya Corp
Priority to JP4105548A priority Critical patent/JP2892213B2/en
Publication of JPH05278041A publication Critical patent/JPH05278041A/en
Application granted granted Critical
Publication of JP2892213B2 publication Critical patent/JP2892213B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/06Hydroxides
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents

Abstract

PURPOSE:To prepare a polyurethane remover having an easy handleability and a superior capability in removing a polyurethane adhering to a molded piece or the like by incorporating a dimethyl sulfoxide with a sodium hydroxide and/or a potassium hydroxide. CONSTITUTION:A polyurethane remover is applied for removing a polyurethane adhering to a molded piece made of a glass or a metal after, esp., a polyurethane lens casted and polymerized is released. In this invention, a polyurethane remover is prepared by incorporating a dimethyl sulfoxide with a sodium hydroxide and/or a potassium hydroxide. As a preferable example, the use ratio of a sodium hydroxide and/or a potassium hydroxide is determined to be 0.01-100 pts.wt. per 1 pts.wt. of a dimethyl sulfoxide. Furthermore, water as a diluent, a carboxylic acid having a cleaning effect, and the like are incorporated. In this manner, the obtained polyurethane remover has an easy handleability and a superior removing capability.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はポリウレタン除去剤に係
り、特にポリウレタンレンズを注型重合して離型させた
後、ガラスまたは金属等で構成されている成形型に付着
しているポリウレタンを除去するのに好適なポリウレタ
ン除去剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyurethane remover, and in particular, it removes the polyurethane adhering to a mold made of glass or metal after cast-polymerizing a polyurethane lens to release it. To a polyurethane remover suitable for

【0002】[0002]

【従来の技術】注型重合にてポリウレタンレンズを製造
することを良く知られている。またポリウレタンレンズ
をガラス又は金属等で構成されている成形型から離型さ
せた場合、前記成形型に前記ポリウレタンレンズの残留
が付着し、この付着物が容易に除去できないことも良く
知られている。この問題を解決する方法として例えば特
開平1−144498号公報にはジメチルスルホキシド
とトリクロロエチレンとを含むポリウレタン除去剤が、
また特開昭58−20422号公報にはジメチルスルホ
キシドに脂肪酸のアミン塩を添加したポリウレタン除去
剤が、さらに特開昭62−243697号公報にはジメ
チルスルホキシドとアルカリ金属有機化合物などからな
る除去剤が開示されている。
It is well known to manufacture polyurethane lenses by cast polymerization. It is also well known that when a polyurethane lens is released from a mold made of glass, metal or the like, the polyurethane lens residue adheres to the mold and the deposit cannot be easily removed. . As a method for solving this problem, for example, JP-A-1-14498 discloses a polyurethane removing agent containing dimethyl sulfoxide and trichlorethylene.
Further, JP-A-58-20422 discloses a polyurethane remover obtained by adding an amine salt of fatty acid to dimethyl sulfoxide, and JP-A-62-243697 discloses a remover comprising dimethyl sulfoxide and an alkali metal organic compound. It is disclosed.

【0003】[0003]

【発明が解決しようとする課題】しかしながら前述した
特開平1−144498号公報に開示されたポリウレタ
ン除去剤は、付着しているポリウレタンを膨潤させる作
用を有しているが、該公報に記載されているようにポリ
ウレタンを溶解させる作用を有していない。このためポ
リウレタンの除去能力が不充分となり、成形型に付着し
ているポリウレタンを完全に除去するには長時間を要す
るという不具合を有する。
However, the polyurethane removing agent disclosed in the above-mentioned JP-A No. 1-14498 has a function of swelling the attached polyurethane, but it is described in this publication. It does not have the action of dissolving polyurethane as it does. Therefore, the ability to remove polyurethane becomes insufficient, and it takes a long time to completely remove the polyurethane attached to the mold.

【0004】また特開昭58−20422号公報に開示
された除去剤は、ポリウレタンの除去能力が不充分で、
該公報にも記載されているように24時間という長い除
去時間を要するという不具合を有する。
Further, the removing agent disclosed in Japanese Patent Application Laid-Open No. 58-20422 has an insufficient ability of removing polyurethane.
As described in this publication, there is a problem that a long removal time of 24 hours is required.

【0005】さらに特開昭62−243697号公報に
開示された除去剤は、ナトリウムハイドライド、カルシ
ウムハイドライドなどのアルカリ金属化有機化合物等を
使用している。これらの物質は湿った空気で分解した
り、水と激しく反応して水素を発生する特性を有してい
る。したがって、この除去剤は取扱いにくいという不具
合を有する。本発明は上述した不具合を解決するために
なされたもので、その目的は取扱いが容易でポリウレタ
ンの除去能力に優れたポリウレタン除去剤を提供するこ
とにある。
Further, the removing agent disclosed in JP-A-62-243697 uses an alkali metallized organic compound such as sodium hydride and calcium hydride. These substances have the property of decomposing in moist air or reacting violently with water to generate hydrogen. Therefore, this remover has a drawback that it is difficult to handle. The present invention has been made to solve the above-mentioned problems, and an object thereof is to provide a polyurethane removing agent which is easy to handle and has excellent polyurethane removing ability.

【0006】[0006]

【課題を解決するための手段】上述した目的は、ジメチ
ルスルホキシドと、水酸化ナトリウムおよび/または水
酸化カリウムとを含むことを特徴とするポリウレタン除
去剤によって達成された。
The above objects have been achieved by a polyurethane scavenger which is characterized in that it contains dimethylsulfoxide and sodium hydroxide and / or potassium hydroxide.

【0007】以下、本発明を詳しく説明する。本発明
は、ジメチルスルホキシド(以下、単に「DMSO」と
いう。)と、水酸化ナトリウムおよび/または水酸化カ
リウムを必須成分とする。(以下、これらの必須成分か
らなる溶液を単に、「必須成分溶液」という場合があ
る。)その理由は、この必須成分の組合せにより取扱い
が比較的容易でポリウレタンの除去能力が従来の除去剤
よりも優れる事を見出したからである。水酸化ナトリウ
ムおよび水酸化カリウムはどちらか1種を用いること、
また混合して用いることができる。その使用割合は限定
されない。
The present invention will be described in detail below. In the present invention, dimethyl sulfoxide (hereinafter, simply referred to as "DMSO") and sodium hydroxide and / or potassium hydroxide are essential components. (Hereinafter, a solution consisting of these essential components may be simply referred to as an "essential component solution".) The reason is that the combination of these essential components makes handling relatively easy and has a polyurethane removal capacity better than that of conventional removers. This is because they have found that they are also superior. Use one of sodium hydroxide and potassium hydroxide,
Further, they can be mixed and used. The usage rate is not limited.

【0008】DMSOと水酸化ナトリウムおよび/また
は水酸化カリウムとの使用割合は、DMSOが1重量部
に対して水酸化ナトリウムおよび/または水酸化カリウ
ムが0.01重量部から100重量部の範囲が好まし
い。その理由は0.01重量部未満、または100重量
部を超えると相乗効果が得られず、充分なポリウレタン
の除去能力を有しないためである。尚、特に好ましい範
囲はDMSOが1重量部に対して水酸化ナトリウムおよ
び/または水酸化カリウムが0.03重量部から0.4
重量部の範囲が好ましい。
The proportion of DMSO and sodium hydroxide and / or potassium hydroxide used is in the range of 0.01 to 100 parts by weight of sodium hydroxide and / or potassium hydroxide to 1 part by weight of DMSO. preferable. The reason is that if it is less than 0.01 parts by weight or more than 100 parts by weight, a synergistic effect cannot be obtained, and sufficient polyurethane removing ability is not obtained. In addition, a particularly preferable range is 0.03 parts by weight of sodium hydroxide and / or potassium hydroxide to 1 part by weight of DMSO to 0.4 parts by weight.
A range of parts by weight is preferred.

【0009】本発明のポリウレタン除去剤は、前述した
必須成分溶液に、必要に応じて任意成分を含有させるこ
とができる。その例として、希釈剤として用いられる
水、また従来より洗浄効果を有すると知られている物
質、例えば、カルボン酸、硫酸塩、リン酸系化合物など
の陰イオン性界面活性剤、アルキレンオキシド化合物、
アミンオキシド、スルホキシドなどの非イオン性界面活
性剤、アミン化合物などの陽イオン性界面活性剤、硝酸
塩、珪酸塩、炭酸塩、ホウ酸塩などの無機酸、塩化ナト
リウム、塩化カリウムなどの塩酸塩、ハロゲンを含む無
機化合物、アルコール、グリセリンなどの酸素含有有機
化合物、アミン化合物、アミド化合物などの窒素含有有
機化合物、リン含有有機化合物、キレート化合物、Si
含有有機化合物が挙げられる。
The polyurethane removing agent of the present invention may contain optional components in the above-mentioned essential component solution, if necessary. As an example thereof, water used as a diluent, or a substance known to have a cleaning effect from the past, for example, carboxylic acid, sulfate, anionic surfactant such as phosphoric acid compound, alkylene oxide compound,
Nonionic surfactants such as amine oxides and sulfoxides, cationic surfactants such as amine compounds, inorganic acids such as nitrates, silicates, carbonates and borates, hydrochlorides such as sodium chloride and potassium chloride, Inorganic compound containing halogen, organic compound containing oxygen such as alcohol and glycerin, organic compound containing nitrogen such as amine compound and amide compound, organic compound containing phosphorus, chelate compound, Si
Including organic compounds.

【0010】本発明のポリウレタン除去剤の使用方法と
しては、例えば、ポリウレタンが付着している成形型、
治工具などを除去剤に浸漬する方法、ポリウレタンが付
着している箇所のみに塗布する方法などが挙げられる
が、好ましい方法は前者の方法である。成形型、治工具
など除去剤に浸漬する際の除去剤の温度は、作業能率、
安全面から20℃から80℃の間が好ましい。その理由
は20℃未満であるとポリウレタンを除去するために浸
漬時間が比較的長くなり、また80℃を超えると除去剤
の取扱いを特に注意しなくてはならないからである。除
去剤の中には、ポリウレタンの除去時間をさらに短くす
るために超音波を振動させることもできる。
The method of using the polyurethane removing agent of the present invention includes, for example, a mold to which polyurethane is attached,
Examples include a method of immersing a jig or the like in a remover and a method of applying only to a place where polyurethane is attached, but the former method is preferable. The temperature of the remover when immersed in the remover such as the mold and jig is
From the viewpoint of safety, it is preferably between 20 ° C and 80 ° C. The reason is that if the temperature is lower than 20 ° C., the dipping time becomes relatively long in order to remove the polyurethane, and if the temperature exceeds 80 ° C., special care must be taken in handling the remover. In some removers, ultrasonic waves can be vibrated to further shorten the removal time of polyurethane.

【0011】本発明のポリウレタン除去剤使用範囲は、
特に限定されないが、ポリウレタンが付着している成形
型および治工具などの除去に好ましく用いられる。ここ
でポリウレタンとは、ポリイソシアネートと、ポリオー
ルおよび/またはポリチオールとを含む単量体混合物を
重合してなるものをいう。このポリイソシアネート、ポ
リオールおよびポリチオールの例示は、特開平3−28
1312号公報、特開平3−236386号公報、特開
平1−144498号公報などによってなされているの
で省略する。本発明のポリウレタン除去剤は特開昭62
−243697号公報に開示されているアルカリ金属化
有機化合物などの危険物を使用することがないので除去
剤の取扱が容易となり、前記必須成分溶液の相乗効果に
より、従来の除去剤よりも短時間で付着したポリウレタ
ンを除去することが可能となる。
The range of use of the polyurethane removing agent of the present invention is
Although not particularly limited, it is preferably used for removing a mold and jigs and the like to which polyurethane is attached. Here, polyurethane means a polymer obtained by polymerizing a monomer mixture containing polyisocyanate and polyol and / or polythiol. Examples of the polyisocyanate, polyol and polythiol are described in JP-A-3-28.
No. 1312, JP-A-3-236386, JP-A-1-14498 and the like are omitted. The polyurethane removing agent of the present invention is disclosed in JP-A-62 / 62.
No dangerous substances such as alkali metallized organic compounds disclosed in JP-A-243697 are used, so that the removal agent can be easily handled, and due to the synergistic effect of the essential component solution, the removal time is shorter than that of the conventional removal agent. It is possible to remove the polyurethane adhered by.

【0012】[0012]

【実施例】以下に本発明の実施例を示すが、本発明をこ
れらの実施例に限定されるものではない。 (実施例1) m−キシレンジイソシアネート…………………………………100重量部 ペンタエリスリトールテトラキス3−メルカプトプロピオネート ………143重量部 リン酸ジn−ブチル………………………………………………6.05重量部 ジブチルスズジラウリン酸………………………………………0.24重量部 2(2′−ヒドロキシ−5′−t−オクチルフェニル)ベンゾトリアゾール ………0.48重量部 上記の混合物を均一に攪拌した後、この混合物3.0g
をガラス型に塗布し、25℃から120℃まで22時間
加熱してガラス型に付着した3.0gのポリウレタンを
得た。このポリウレタンが付着したガラス型全体を、ジ
メチルスルホキシド(DMSO) 40重量部、水 6
0重量部、水酸化ナトリム 8重量部を混合した除去剤
に除去剤温度70±2℃の条件下で浸漬し、5分ごとに
前記ガラス型を引き上げ風乾してポリウレタンの除去率
を測定した。その結果を表1に示す。表1に示すように
5分で22%、10分で48%、15分で75%、20
分で98%除去され、ポリウレタンの除去能力に優れた
除去剤であることが確認された。また、この除去剤は気
体の発生が見受けられなかった。
EXAMPLES Examples of the present invention will be shown below, but the present invention is not limited to these examples. (Example 1) m-xylene diisocyanate: 100 parts by weight pentaerythritol tetrakis-3-mercaptopropionate: 143 parts by weight di-n-butyl phosphate: ………………………………………… 6.05 parts by weight Dibutyltin dilauric acid …………………………………… 0.24 parts by weight 2 (2'-hydroxy-) 5'-t-octylphenyl) benzotriazole ... 0.48 parts by weight After uniformly stirring the above mixture, 3.0 g of this mixture was added.
Was applied to a glass mold and heated from 25 ° C. to 120 ° C. for 22 hours to obtain 3.0 g of polyurethane adhered to the glass mold. 40% by weight of dimethylsulfoxide (DMSO) and water 6
The removal rate of polyurethane was measured by immersing in a remover mixed with 0 part by weight and 8 parts by weight of sodium hydroxide under the condition of a remover temperature of 70 ± 2 ° C., pulling up the glass mold every 5 minutes and air drying. The results are shown in Table 1. As shown in Table 1, 22% in 5 minutes, 48% in 10 minutes, 75% in 15 minutes, 20%
It was confirmed to be a scavenger having an excellent ability of removing polyurethane by 98% in minutes. Further, no gas was found to be generated with this remover.

【0013】(実施例2)実施例1で用いた水酸化ナト
リウム 8重量部の代わりに、水酸化カリウム11.2
重量部を用いた以外はすべて実施例1同様に行った。評
価結果を表1に示す。表1に示すよう実施例2で得られ
た除去剤は実施例1で得られた除去剤同様、除去能力に
優れたものであった。
Example 2 Instead of 8 parts by weight of sodium hydroxide used in Example 1, potassium hydroxide 11.2 was added.
Example 1 was repeated except that the parts by weight were used. The evaluation results are shown in Table 1. As shown in Table 1, the removing agent obtained in Example 2 was as excellent in removing ability as the removing agent obtained in Example 1.

【0014】(実施例3)実施例1で用いた水酸化ナト
リウム 8重量部の代わりに、水酸化ナトリウム4重量
部、および水酸化カリウム 5.6重量部を用いた以外
はすべて実施例1同様に行った。その結果、表1に示す
よう実施例3で得られた除去剤は実施例1で得られた除
去剤同様、除去能力に優れたものであった。
Example 3 All were the same as Example 1 except that 4 parts by weight of sodium hydroxide and 5.6 parts by weight of potassium hydroxide were used instead of 8 parts by weight of sodium hydroxide used in Example 1. Went to. As a result, as shown in Table 1, the removing agent obtained in Example 3 was as excellent in removing ability as the removing agent obtained in Example 1.

【0015】(比較例1)本発明の除去剤と比較する例
として特開平1−144498号公報に開示されている
除去剤を挙げる。実施例1で用いた水 60重量部、水
酸化ナトリウム 8重量部を用いず、代わりにトリクロ
ロエチレン 80重量部を用いた以外は、すべて実施例
1と同様に行った。その結果を表2に示す。表2に示す
よう比較例1の除去剤は20分浸漬してもポリウレタン
が除去されないものであった。
(Comparative Example 1) As an example for comparison with the removing agent of the present invention, the removing agent disclosed in JP-A-1-14498 will be mentioned. The procedure of Example 1 was repeated except that 60 parts by weight of water and 8 parts by weight of sodium hydroxide used in Example 1 were not used, and 80 parts by weight of trichlorethylene was used instead. The results are shown in Table 2. As shown in Table 2, the removing agent of Comparative Example 1 did not remove the polyurethane even after being immersed for 20 minutes.

【0016】(比較例2)除去剤としてDMSOのみを
用いた場合のポリウレタンの除去能力を比較例2で示
す。実施例1で用いた水 60重量部、水酸化ナトリム
8重量部を用いなかった以外はすべて実施例1と同様
に行った。その結果を表2に示す。表2に示すよう比較
例2の除去剤は20分浸漬してもポリウレタンが除去さ
れないものであった。尚、表1、表2における除去率は
以下の式より求めた。
(Comparative Example 2) Comparative Example 2 shows the removing ability of polyurethane when only DMSO is used as a removing agent. The same procedure as in Example 1 was carried out except that 60 parts by weight of water and 8 parts by weight of sodium hydroxide used in Example 1 were not used. The results are shown in Table 2. As shown in Table 2, the removing agent of Comparative Example 2 did not remove the polyurethane even after soaking for 20 minutes. The removal rates in Tables 1 and 2 were calculated by the following formula.

【0017】(比較例3)除去剤としてDMSOを用い
ない場合のポリウレタンの除去能力を比較例3で示す。
実施例1で用いたDMSO 40重量部を用いずに、水
100重量部、水酸化カリウム 5.6重量部を用い
て除去剤を作製した以外はすべて実施例1と同様に行っ
た。その結果を表2に示す。表2に示すよう比較例3の
除去剤は20分浸漬してもポリウレタンが除去されない
ものであった。
(Comparative Example 3) Comparative Example 3 shows the removing ability of polyurethane when DMSO is not used as a removing agent.
The same procedure as in Example 1 was carried out except that the removing agent was prepared using 100 parts by weight of water and 5.6 parts by weight of potassium hydroxide instead of 40 parts by weight of DMSO used in Example 1. The results are shown in Table 2. As shown in Table 2, the removing agent of Comparative Example 3 did not remove the polyurethane even after being immersed for 20 minutes.

【0018】(比較例4)除去剤として水酸化ナトリウ
ム、水酸化カリウムの代わりに弱アルカリ成分の炭酸水
素カリウムを用いた場合のポリウレタンの除去能力を比
較例4で示す。実施例1で用いた水酸化ナトリウム8重
量部の代わりに炭酸水素カリウム20重量部を用いて除
去剤を作製した以外はすべて実施例1と同様に行った。
その結果を表2に示す。表2に示すよう比較例4の除去
剤は20分浸漬してもポリウレタンが除去されないもの
であった。
(Comparative Example 4) Comparative Example 4 shows the removal ability of polyurethane when weak alkaline component potassium hydrogencarbonate is used in place of sodium hydroxide and potassium hydroxide as a removing agent. The procedure of Example 1 was repeated except that 20 parts by weight of potassium hydrogen carbonate was used instead of 8 parts by weight of sodium hydroxide used in Example 1 to prepare the removing agent.
The results are shown in Table 2. As shown in Table 2, the remover of Comparative Example 4 was such that the polyurethane was not removed even after being immersed for 20 minutes.

【0019】(比較例5)除去剤として水酸化ナトリウ
ム、水酸化カリウムの代わりに弱酸性成分の酢酸ナトリ
ウムを用いた場合のポリウレタンの除去能力を比較例5
で示す。実施例1で用いた水酸化ナトリウム8重量部の
代わりに酢酸ナトリウム27重量部を用いて除去剤を作
製した以外はすべて実施例1と同様に行った。その結果
を表2に示す。表2に示すよう比較例5の除去剤は20
分浸漬してもポリウレタンが除去されないものであっ
た。
(Comparative Example 5) Comparative Example 5 shows the removal ability of polyurethane when weakly acidic component sodium acetate is used in place of sodium hydroxide and potassium hydroxide as a removing agent.
Indicate. The procedure of Example 1 was repeated except that 27 parts by weight of sodium acetate was used instead of 8 parts by weight of sodium hydroxide used in Example 1 to prepare the removing agent. The results are shown in Table 2. As shown in Table 2, the removal agent of Comparative Example 5 was 20
The polyurethane was not removed even after immersion for a minute.

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【表2】 [Table 2]

【0022】[0022]

【発明の効果】以上、上述したように、本発明の除去剤
は、水素などの気体が発生しないので取扱が容易で、さ
らに従来の除去剤と比べポリウレタンの除去能力に優れ
る。
As described above, since the removing agent of the present invention does not generate a gas such as hydrogen, it is easy to handle, and is excellent in polyurethane removing ability as compared with the conventional removing agents.

フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 B29K 75:00 Continuation of the front page (51) Int.Cl. 5 Identification number Office reference number FI technical display area B29K 75:00

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ジメチルスルホキシドと、水酸化ナトリ
ウムおよび/または水酸化カリウムとを含むことを特徴
とするポリウレタン除去剤。
1. A polyurethane remover comprising dimethyl sulfoxide and sodium hydroxide and / or potassium hydroxide.
JP4105548A 1992-03-31 1992-03-31 Polyurethane remover Expired - Fee Related JP2892213B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4105548A JP2892213B2 (en) 1992-03-31 1992-03-31 Polyurethane remover

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4105548A JP2892213B2 (en) 1992-03-31 1992-03-31 Polyurethane remover

Publications (2)

Publication Number Publication Date
JPH05278041A true JPH05278041A (en) 1993-10-26
JP2892213B2 JP2892213B2 (en) 1999-05-17

Family

ID=14410632

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4105548A Expired - Fee Related JP2892213B2 (en) 1992-03-31 1992-03-31 Polyurethane remover

Country Status (1)

Country Link
JP (1) JP2892213B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001098191A (en) * 1999-07-23 2001-04-10 Toray Fine Chemicals Co Ltd Composition for peeling organic coating film
US6568406B2 (en) * 1997-10-22 2003-05-27 Basf Aktiengesellschaft Method of cleaning plant parts for the preparation or processing of (meth)acrylic esters
JP2014125531A (en) * 2012-12-26 2014-07-07 Kaneko Kagaku:Kk Solvent composition for resin removal
KR101507530B1 (en) * 2013-09-27 2015-04-07 주식회사 금오공업 Separation chemical mixture and mechanical method of urethane film from automotive instrument panel skin for TPO recycle
WO2017126652A1 (en) * 2016-01-20 2017-07-27 日揮プラントイノベーション株式会社 Liquid detergent composition for removing sludge and hard films formed in system containing heavy hydrocarbon or element imparting polarity to molecule, and cleaning method using same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61848A (en) * 1984-06-14 1986-01-06 Nec Corp Bus selection system for decentralized control system
JPH01144498A (en) * 1987-11-30 1989-06-06 Hoya Corp Polyurethane-removing agent

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61848A (en) * 1984-06-14 1986-01-06 Nec Corp Bus selection system for decentralized control system
JPH01144498A (en) * 1987-11-30 1989-06-06 Hoya Corp Polyurethane-removing agent

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6568406B2 (en) * 1997-10-22 2003-05-27 Basf Aktiengesellschaft Method of cleaning plant parts for the preparation or processing of (meth)acrylic esters
JP2001098191A (en) * 1999-07-23 2001-04-10 Toray Fine Chemicals Co Ltd Composition for peeling organic coating film
JP2014125531A (en) * 2012-12-26 2014-07-07 Kaneko Kagaku:Kk Solvent composition for resin removal
KR101507530B1 (en) * 2013-09-27 2015-04-07 주식회사 금오공업 Separation chemical mixture and mechanical method of urethane film from automotive instrument panel skin for TPO recycle
WO2017126652A1 (en) * 2016-01-20 2017-07-27 日揮プラントイノベーション株式会社 Liquid detergent composition for removing sludge and hard films formed in system containing heavy hydrocarbon or element imparting polarity to molecule, and cleaning method using same
JPWO2017126652A1 (en) * 2016-01-20 2019-01-31 日揮プラントイノベーション株式会社 Cleaning liquid composition for removing sludge and hardened film produced in system containing heavy hydrocarbon or element that gives polarity to molecule, and cleaning method using the same

Also Published As

Publication number Publication date
JP2892213B2 (en) 1999-05-17

Similar Documents

Publication Publication Date Title
CA1235634A (en) Aqueous alkaline paint stripping compositions
US4377489A (en) Inorganic persulfate cleaning solution for acoustic materials
TWI386765B (en) Dynamic multi-purpose composition for the removal of photoresists and method for its use
JP2683729B2 (en) Alkali-containing photoresist stripping composition with reduced metal corrosion having cross-linked or cured resist resin
CA2190183C (en) Aluminum desmut composition and process
WO1996030488A9 (en) Aluminum desmut composition and process
EP0656405A2 (en) Aqueous stripping compositions containing a hydroxylamine and an alkanolamine and use thereof
JP2001520118A (en) Aqueous stripping and cleaning compositions
KR20090037088A (en) Resist stripper composition and a method of stripping resist using the same
US7699940B2 (en) Flushing solutions for coatings removal
JPH05278041A (en) Polyurethane remover
CA2200615C (en) Stainless steel alkali treatment
CN111978810A (en) Method for producing coating material and coating material
US3663476A (en) Alkaline stripping composition and process
JPH06248206A (en) Cleaning agent composition for removing protective coating film
KR20190121073A (en) Rust remover and its composition
JP3806869B2 (en) Descaler and inhibitor
US3563900A (en) Paint stripping composition and method
JPH10292138A (en) Composition for peeling off coated film
JPH0427472A (en) Washing method for resin molding
JPH06107984A (en) Cleaning agent for removing protective coating film
JPS6148583A (en) Scale remover
JPH11172300A (en) Cleaner composition for plastic lens molding glass mold
JP2792263B2 (en) Non-halogen cleaning agent used for cleaning the release agent attached to synthetic resin moldings
SU633896A1 (en) Composition for removing scale from enamelled metal surface

Legal Events

Date Code Title Description
A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 19971111

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080226

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090226

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100226

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100226

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110226

Year of fee payment: 12

LAPS Cancellation because of no payment of annual fees