JPS5885826A - Stabilization method of methylene chloride - Google Patents

Stabilization method of methylene chloride

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Publication number
JPS5885826A
JPS5885826A JP18439081A JP18439081A JPS5885826A JP S5885826 A JPS5885826 A JP S5885826A JP 18439081 A JP18439081 A JP 18439081A JP 18439081 A JP18439081 A JP 18439081A JP S5885826 A JPS5885826 A JP S5885826A
Authority
JP
Japan
Prior art keywords
methylene chloride
combination
stabilizer
metal
methanol
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
JP18439081A
Other languages
Japanese (ja)
Inventor
Hideji Baba
馬場 秀治
Nobuyuki Yoshimura
吉村 信行
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.)
Tokuyama Corp
Original Assignee
Tokuyama 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 Tokuyama Corp filed Critical Tokuyama Corp
Priority to JP18439081A priority Critical patent/JPS5885826A/en
Publication of JPS5885826A publication Critical patent/JPS5885826A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE:To prevent the decomposition of methylene chloride and further the corrosion of metal in the vapor and liquid phase parts in the washing step of the metal with steam, by adding a combination of methanol, an aliphatic amine, epoxide and phenol to the methylene oxide. CONSTITUTION:0.01-1.0wt% methanol, 0.005-0.5wt% aliphatic amine, e.g. diisobutylamine, 0.01-1.0wt% epoxide, e.g. propylene oxide, and 0.001-0.05wt% phenol, e.g. eugenol, are added to prevent the decomposition of methylene chloride. In particular, a stabilizer for the methylene chloride used in washing metal with steam is required to satisfy the above-mentioned combination, and the absence of even one component of the combination remarkably reduces the effect thereof.

Description

【発明の詳細な説明】 本楯明は塩化メチレンの安定化方法に員する。[Detailed description of the invention] This book concerns the method for stabilizing methylene chloride.

詳しくは塩化メチレンに対してメタ−ノール、11肪族
アミン類、工4キサイド類及びフェノール類を添加する
塩化メチレンの安定化方法である。
Specifically, it is a method for stabilizing methylene chloride in which methanol, 11-aliphatic amines, 4-oxides, and phenols are added to methylene chloride.

塩素化炭化水素は一般Kll媒、#l剤として広く使用
されている。一般に、塩素化炭化水嵩の純粋なものは比
較的安定な化合物であるが、工業的に製造され九製品が
光、空気、水分、油、熱等の影響下に金ll4Iiと接
触する場合、塩素化炭化水素が4解する。そのために従
来より種々の安定剤が一発され、単一で或いは数種の組
合せで使用されている。しかしながら塩素化炭化水素は
種1m1によってその分解機構が異なるため、全ての塩
素化炭化水素に効果のある安定剤は存在せず、塩素化炭
化水素の種類に応じて使用する安定剤の組合せも開発さ
れている0例えば/臂−クロルエチレン、トリクロルエ
チレン等の不飽和塩素化炭化水素の安定剤を2塩化エタ
ン、3塩化エタン等の飽和塩素化炭化水素に転用しても
安定化効果は全く期待出来ない。ま九飽和塩素化炭化水
素にあってもメチルクロロホルム、ジクロルエタン、[
化メfし7等それぞれの分解機構が異なシ同じ安定剤を
用いることが出来ない。従って各塩素化炭化水素の種類
に応じて適当な安定剤の組合せが開発されるのが現状で
ある。
Chlorinated hydrocarbons are widely used as general Kll and #l agents. In general, pure chlorinated hydrocarbons are relatively stable compounds, but when industrially produced products come into contact with gold under the influence of light, air, moisture, oil, heat, etc., chlorine Hydrocarbons are divided into 4 parts. For this purpose, various stabilizers have been developed and used singly or in combination. However, since the decomposition mechanism of chlorinated hydrocarbons differs depending on the species per ml, there is no stabilizer that is effective against all chlorinated hydrocarbons, and we have developed combinations of stabilizers to be used depending on the type of chlorinated hydrocarbon. For example, even if stabilizers for unsaturated chlorinated hydrocarbons such as chlorethylene and trichlorethylene are used for saturated chlorinated hydrocarbons such as dichloroethane and trichlorethane, no stabilizing effect can be expected. Can not. Even among saturated chlorinated hydrocarbons, methyl chloroform, dichloroethane, [
It is not possible to use the same stabilizer because the decomposition mechanisms are different for each type of stabilizer, such as 7. Therefore, at present, appropriate combinations of stabilizers are developed depending on the type of each chlorinated hydrocarbon.

上述した塩素化炭化水素のうち塩化メチレンは他の塩素
化炭化水素に比較すると着しく安定性が良好なため安定
剤を添加する必要があるi用分野は少なかった。しかし
ながら、該塩化メチレンを金属の蒸気洗浄用溶剤として
使用する際に塩化メチレンが多少分解し1分解物により
金属の腐食が生ずる傾向がある。
Among the above-mentioned chlorinated hydrocarbons, methylene chloride is relatively stable and has good stability compared to other chlorinated hydrocarbons, so there are few fields where it is necessary to add a stabilizer. However, when the methylene chloride is used as a solvent for steam cleaning of metals, the methylene chloride tends to decompose to some extent and the decomposed products tend to cause corrosion of metals.

本@咽者等ri、塩化メチレンによる金属の蒸気洗浄に
おいて本塩化メチレンを安定化し得る安定剤の開発に鋭
意研究を重ねた。その結果、メタノール、脂肪族アミン
類、ニーキサイド類及びフェノール類の組合せが上記金
属の蒸気洗浄における塩化メチレンの分解を極めて効果
的に防止し、該金属の蒸気洗弗を行なう場合に気相部及
び敵相部に存在する金属の腐食を防止できることを見い
出し本発明を完成するに至った。
We have conducted intensive research to develop a stabilizer that can stabilize methylene chloride during steam cleaning of metals with methylene chloride. As a result, the combination of methanol, aliphatic amines, nixides, and phenols very effectively prevents the decomposition of methylene chloride during steam cleaning of the metals, and when steam cleaning the metals, the gas phase and The present invention was completed by discovering that it is possible to prevent corrosion of metals present in the enemy phase.

本発明は塩化メチレンに対してメタノール、脂肪族アミ
ン類、エポキサイド類及びフェノール類を添加する塩化
メチレンの安定化方法である。
The present invention is a method for stabilizing methylene chloride by adding methanol, aliphatic amines, epoxides, and phenols to methylene chloride.

本発明で用いる脂肪族アミン類は他の塩素化炭化水素の
安定剤成分として公知の脂肪族アミン畑が特に限定され
ず用いうる。一般にはグイツブチルアミン、ジインゾロ
ビルアミン等のジイソアルキルアミンが最も効果的であ
り、塩化メチレンの着色上の心配もなく好適である。
The aliphatic amines used in the present invention may be any known aliphatic amines used as stabilizer components for other chlorinated hydrocarbons without particular limitation. In general, diisoalkylamines such as guitubutylamine and diinzolobylamine are the most effective, and are suitable because they do not have to worry about coloring caused by methylene chloride.

また、本発明で用いるエポキサイド類は公知のものが特
に制限なく使用される0例えばプロピレンオキサイド、
ブチレンオキサイド等が一般に用いられる。
In addition, as the epoxides used in the present invention, known ones can be used without particular restriction. For example, propylene oxide,
Butylene oxide and the like are commonly used.

更にまえ本発明で用いるフェノール類は1例オーばフェ
ノール、チモール、カテコール、ノヤラクレゾール、オ
イrノール、インオイゲノール等が一般に使用される。
Furthermore, the phenols used in the present invention include, for example, phenol, thymol, catechol, noyalacresol, eugenol, and eugenol.

本発明に於ける前記安定剤の添加量は塩化メチレンの使
用分野、使用条件、安定剤の種類等により異なり一部に
限定的ではなく必要に応じて予め決定すればよい。
The amount of the stabilizer added in the present invention varies depending on the field of use of methylene chloride, the conditions of use, the type of stabilizer, etc., and is not limited to any particular part, but may be determined in advance as necessary.

一般にメタノールは塩化メチレンに対して。Generally methanol is relative to methylene chloride.

0.00/〜2.0重量%、好ましくけo、oi〜/、
0重量部、また脂肪族アミン類は塩化メチレンに対して
O0θOノ〜コ、θ重t−,好ましくFio、oos〜
0.5重量−の範囲から選べば十分である。更にエポキ
サイド類FiO、00/〜コ、O重量−から、好ましく
liO,01〜i、0重iisの範囲から選べば十分で
ある。更にまた。
0.00/~2.0% by weight, preferably o, oi~/,
0 parts by weight, and the aliphatic amines are O0θOno~ko, θweight t-, preferably Fio, oos~ with respect to methylene chloride.
It is sufficient to select from a range of -0.5 weight. Furthermore, it is sufficient to select from the range of epoxides FiO, 00/~ko, O weight-, preferably from the range of liO, 01~i, 0 weight iis. Yet again.

フェノール類はO0θO7〜O07重量憾好ましくFi
o、θO/〜o、os重量5−の範囲内で添加すればよ
い。
Phenols are O0θO7~O07 weight, preferably Fi
It may be added within the range of o, θO/ to o, os weight 5-.

本発明における安定剤成分の一部は、他の成分と組合せ
て塩化メチレン及び他の塩素化炭化水嵩の安定剤として
公知である。しかし表から、後述する実施例及び比較例
より明らかな如く、I#に金属の蒸気洗浄に用いる塩化
メチレンの安定剤としては本発明の前記成分の組合せを
満足するととにより初めて一部な効果が見られ、この組
合せの一成分を欠い丸紐合せにおいてはそめ効果が著し
く低下する。*見切の前記成分の組合せによりこのよう
な優れた安定化効果を発揮する観構については未だ明ら
かではない。
Some of the stabilizer components in this invention are known as methylene chloride and other chlorinated hydrocarbon bulk stabilizers in combination with other components. However, as is clear from the table and the Examples and Comparative Examples described below, I# as a stabilizer for methylene chloride used for steam cleaning of metals can only be partially effective when the above-mentioned combination of components of the present invention is satisfied. However, when one component of this combination is missing and the round string combination is used, the reduction effect is significantly reduced. *It is not yet clear how the combination of the above-mentioned components of the cutout exhibits such an excellent stabilizing effect.

本発明を更に具体的に説明するため以下実施例及び比較
例を挙げて説明するが不発@はこれらの実施例に限定さ
れる本のではない。
In order to explain the present invention more specifically, the present invention will be described below with reference to Examples and Comparative Examples, but the book is not limited to these Examples.

実施例及び比較例 塩化メチレン2!;081に対して第1表に示す紐取、
及び量の安定剤、及び水3−を添加して試験液を・11
1111IL、該試験液を300dの丸底フラスコに入
れた後、/QQMIのソックスレー抽出器ヲ該丸鷹フラ
スコに取〕付けた。同、丸底フラスコとノックスレニ抽
出器の中にはそれぞれ表、面をよく磨いた亜鉛片を存在
させた。上記丸底フラスコを水浴上で加熱して塩化メチ
ルンをS日間連続沸騰還流させて、塩化メチレンの安定
性試験を行なり九、塩化メチレンの安定性は試験前及び
試験終了後に試験液と等量の蒸留水で試験液を抽出して
得られた水相の−を測定すると共に前記丸底フラスコ及
びソックスレー抽出器の中の亜鉛片の表面状態をI’l
lて評価し友、結果をIg/表に併せて示す、f4、亜
鉛片の表面状態の評価は下記の判定規準に基づいて行な
り九。
Examples and Comparative Examples Methylene chloride 2! ;Hitori shown in Table 1 for 081,
and an amount of stabilizer, and water to prepare the test solution.
1111IL, the test solution was placed in a 300 d round bottom flask, and a /QQMI Soxhlet extractor was attached to the round hawk flask. Similarly, inside the round-bottomed flask and the Noxleni extractor, there were zinc pieces with well-polished surfaces. A stability test of methylene chloride was carried out by heating the above round bottom flask on a water bath and boiling and refluxing methyl chloride for S days continuously. The test solution was extracted with distilled water, and the resulting aqueous phase was measured for -, and the surface condition of the zinc pieces in the round bottom flask and Soxhlet extractor was measured.
The results are also shown in the Ig/Table. The surface condition of the zinc piece was evaluated based on the following criteria.

O:試験片が全く変化しない。O: The test piece did not change at all.

0:試験片の一部に曇9が認められる。0: Cloudiness 9 is observed in a part of the test piece.

′Δ:試験片の一部に明らかな腐食が認められる。'Δ: Clear corrosion is observed in a part of the test piece.

X:試験片の全面にわたって腐食が認められる。X: Corrosion is observed over the entire surface of the test piece.

Claims (1)

【特許請求の範囲】[Claims] 塩化メチレンに、メタノール、脂肪族アミン類、工4キ
サイド類及びフェノール類を添加することをI!#像と
する塩化メチレンの安定化方法。
Adding methanol, aliphatic amines, tetraoxides, and phenols to methylene chloride is I! # Method for stabilizing methylene chloride as an image.
JP18439081A 1981-11-19 1981-11-19 Stabilization method of methylene chloride Pending JPS5885826A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18439081A JPS5885826A (en) 1981-11-19 1981-11-19 Stabilization method of methylene chloride

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18439081A JPS5885826A (en) 1981-11-19 1981-11-19 Stabilization method of methylene chloride

Publications (1)

Publication Number Publication Date
JPS5885826A true JPS5885826A (en) 1983-05-23

Family

ID=16152338

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18439081A Pending JPS5885826A (en) 1981-11-19 1981-11-19 Stabilization method of methylene chloride

Country Status (1)

Country Link
JP (1) JPS5885826A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62158228A (en) * 1985-12-28 1987-07-14 Tokuyama Soda Co Ltd Methylene chloride composition
JP2012041289A (en) * 2010-08-18 2012-03-01 Tokuyama Corp Method of producing chloropropane
WO2014185321A1 (en) * 2013-05-13 2014-11-20 昭和電工株式会社 Purification method for dichloromethane, and production method for difluoromethane using said purification method

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62158228A (en) * 1985-12-28 1987-07-14 Tokuyama Soda Co Ltd Methylene chloride composition
JP2012041289A (en) * 2010-08-18 2012-03-01 Tokuyama Corp Method of producing chloropropane
WO2014185321A1 (en) * 2013-05-13 2014-11-20 昭和電工株式会社 Purification method for dichloromethane, and production method for difluoromethane using said purification method
JP2014221727A (en) * 2013-05-13 2014-11-27 昭和電工株式会社 Dichloromethane purification method and method of producing difluoromethane using the same

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