JPS61143331A - Stabilization of solvent - Google Patents

Stabilization of solvent

Info

Publication number
JPS61143331A
JPS61143331A JP26463584A JP26463584A JPS61143331A JP S61143331 A JPS61143331 A JP S61143331A JP 26463584 A JP26463584 A JP 26463584A JP 26463584 A JP26463584 A JP 26463584A JP S61143331 A JPS61143331 A JP S61143331A
Authority
JP
Japan
Prior art keywords
solvent
nitroethane
nitromethane
methylmorpholine
benzotriazole
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
JP26463584A
Other languages
Japanese (ja)
Other versions
JPH0531530B2 (en
Inventor
Megumi Furuno
恵 古野
Nobuaki Imamori
信秋 今森
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP26463584A priority Critical patent/JPS61143331A/en
Publication of JPS61143331A publication Critical patent/JPS61143331A/en
Publication of JPH0531530B2 publication Critical patent/JPH0531530B2/ja
Granted legal-status Critical Current

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

Abstract

PURPOSE:To obtain a solvent having improved chemical stability, free from corrosivity to metallic materials such as copper, zinc, iron, etc., and most suitable as a cleaning agent, by adding a stabilizer selected from N- methylmorpholine, benzotiazole, nitromethane and nitroethane to a solvent. CONSTITUTION:1,2-Dichloro-1,1-difluoroethane (abbreviated as flon 1326) useful as a cleaning agent for various articles because of its inccombustibility, low toxicity, excellent solubility and moderate boiling point, is stabilized by the addition of one or more components selected from N-methylmorpholine, benzotriazole, nitromethane and nitroethane. Preferably, the amount of N- methylmorpholine, nitromethane or nitroethane is <=5 vol%, and that of benzotriazole is <=3,000 ppm (wt) based on the solvent.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、1,2−ジクロロ−1,1−シフA/オロエ
タン(以下、フロン162bと称する)の安定化法に関
するC フロン132bは不燃性で低毒性であり、またすぐれた
溶解能と適度の沸点を有するため、種々の物・品の洗浄
剤として利用できる。たとえば、シリコーンウェハーや
シ11コンチップ等の半導体材料、IOやL8工等の半
導体類、プリント配線基板、リレースイッチ、マイクロ
モーター等のt子−を気機器類、時計、カメラ、マイク
ロベアリング、レンズ等の精密機器類の脱脂洗浄剤Kl
f用である。
Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a method for stabilizing 1,2-dichloro-1,1-Schiff A/oloethane (hereinafter referred to as Freon 162b). It is highly resistant to water, has low toxicity, and has excellent solubility and a moderate boiling point, so it can be used as a cleaning agent for a variety of items. For example, semiconductor materials such as silicone wafers and silicon chips, semiconductors such as IO and L8, printed wiring boards, relay switches, micro motors, etc., mechanical equipment, watches, cameras, micro bearings, lenses, etc. Degreasing cleaner Kl for precision instruments
It is for f.

(従来の技術) フロン132bはり実には未だ産業界で実用的には用い
られておらず、その特性については未知な部分が多い。
(Prior Art) Freon 132b has not yet been practically used in industry, and there are many unknowns about its characteristics.

中でも弗素原子もしくは水素原子を含まない従来の塩素
系溶剤や弗素系溶剤とは異なった分解挙動ン示すため、
その安定化には未だ充分な方法が知られていない。
Among them, it exhibits a decomposition behavior different from conventional chlorine-based solvents and fluorine-based solvents that do not contain fluorine or hydrogen atoms.
A sufficient method for its stabilization is not yet known.

(発明が解決しようとする問題点) フロン132t)はメチルクロロホルム、テトラクロル
エチレン、トリクロルエチレン等ノ塩素系溶剤に較べて
安定性が高く、一般の使用条件下では安定化は必ずしも
必要でないが、それでも水分 −が共存する場合とか、
電子機器や精密I!器類の洗浄のように品質要求水準が
高度で厳密である場合には、その安定性が問題となるこ
とがある。特に電子・電気機器や精密機器類において多
用されて(・る銅、亜鉛、鉄等の金属材料の存在下で溶
剤の劣化が起るときけ、同時にこれらの金属の腐蝕tひ
き岨すことになり、被洗物の品質に悪影響を与える。
(Problems to be Solved by the Invention) Freon 132t) is more stable than chlorinated solvents such as methyl chloroform, tetrachloroethylene, and trichloroethylene, and stabilization is not necessarily required under general usage conditions. However, in cases where moisture coexists,
Electronic equipment and precision I! When the required quality level is high and strict, such as when cleaning equipment, stability may become a problem. In particular, it is frequently used in electronic/electrical equipment and precision equipment (・When deterioration of the solvent occurs in the presence of metal materials such as copper, zinc, and iron, it also causes corrosion of these metals. This will adversely affect the quality of the items being washed.

(問題点!解決するための手段) 本発明者等は、フロン132bの安定性を改善しようと
して種々検討7重ねた結果、その方法を見出し本発明に
到達した。
(Problem! Means for Solving) The present inventors have conducted various studies in an attempt to improve the stability of Freon 132b, and as a result, have found a method and arrived at the present invention.

すなわち、本発明は、フロン132bKN−メチルモル
ホリン、ペン1戸トリア1戸−ル、ニトロメタンおよび
ニトロエタンから選ばれる安定剤の一種または二種以上
?添加することン特徴とするフロン132bの安定化方
法である。本発明における安定剤の添加量については特
に限定されないが、通常、N−メチルモルホリン、ニト
ロメタン、ニトロエタンについては溶剤に対し5容量俤
以下、ペン・戸トリア・戸−ルについては溶剤に対し3
000重量ppm以下である。添加量がこれより多いと
きは液が着色したり、不溶物となって析出したり、引火
性が生じたりして得策でない。また、本発明の方法はフ
ロン132tl’主成分とする混合溶剤に対しても適用
できる、つまりフロン162bの溶剤特性ン著しく変え
ない範囲において、メタノール、エタノール、インゾロ
パノール、インブタノール、  tart−ブタノール
、アセトン、メチル・エチケトン、酢酸エチル、メチレ
ンクロライr等ケフロン132t)K少量部加えた混合
溶剤についてもその適用が可能である、 (発明の効果) 本発明によって安定化されたフロン132bおよびその
混合溶剤は極めて化学的安定性が高く、′銅、亜鉛、鉄
等の金属材料i腐蝕させることが少ないので、各分野に
おける洗浄畑として幅広く使用することができる。
That is, the present invention provides one or more stabilizers selected from Freon 132bKN-methylmorpholine, Pentritriol, nitromethane, and nitroethane. This is a method for stabilizing Freon 132b, which is characterized by addition. The amount of stabilizer added in the present invention is not particularly limited, but usually, for N-methylmorpholine, nitromethane, and nitroethane, it is less than 5 volumes per solvent, and for pens, doors, and doors, it is 3 volumes per solvent.
000 ppm by weight or less. If the amount added is larger than this, it is not a good idea because the liquid may become colored, become precipitated as insoluble matter, or become flammable. Furthermore, the method of the present invention can also be applied to mixed solvents containing Freon 132tl' as the main component, i.e., methanol, ethanol, inzolopanol, imbutanol, tart-butanol, acetone, as long as the solvent properties of Freon 162b are not significantly changed. , methyl ethiketone, ethyl acetate, methylene chloride r, etc. Keflon 132t) can also be applied to a mixed solvent containing a small amount of K. (Effects of the invention) Flon 132b stabilized by the present invention and its mixed solvent It has extremely high chemical stability and rarely corrodes metal materials such as copper, zinc, and iron, so it can be widely used as a cleaning field in various fields.

(実施例) 以下に本発明ン実施例によって説明する。(Example) The present invention will be explained below using examples.

なお、実施例における安定性試、験は次の方法によって
行なわれた。また安定剤は次の略号で示す。
Incidentally, the stability tests and tests in the Examples were conducted by the following method. Stabilizers are indicated by the following abbreviations.

N−メチルモルホリン:  NMM ニトロメタン    :NM ニトロエタン    二NB ベンψトリア1戸−ル :  BTA 安定性試@i: 試料5Qmを容量100dのがラスび
んに入れ、これに充分によく磨いた亜鉛、鋼、鉄等の金
属試験片を、その下半分が液相部につかるように入れ【
密閉し、60℃で96時間処理する。金属片の腐蝕状態
ン気相部に露出した部分と液相部に浸漬した部分にわけ
て観察する、実施例1 水分v800111ppm含むフo y 132 t’
および表−1に示す各種安定剤を加えたものt試料とし
、金属試験片として亜鉛を用いて安定性状mV行なった
。また、比較のため安定剤を加えないフロン1321)
Kついても安定性試験を行った、その結果7表−1に示
す。
N-methylmorpholine: NMM Nitromethane: NM Nitroethane 2NB Ben ψ tria 1 unit: BTA Stability test @i: Sample 5Qm was placed in a glass bottle with a capacity of 100 d, and thoroughly polished zinc, steel, Place a metal test piece such as iron so that its lower half touches the liquid phase [
Seal and process at 60°C for 96 hours. Example 1 Corrosion state of metal piece: Observed separately in the part exposed to the gas phase and the part immersed in the liquid phase.
The various stabilizers shown in Table 1 were added to prepare T samples, and the stability mV was conducted using zinc as a metal test piece. Also, for comparison, Freon 1321 (without adding stabilizer)
A stability test was also conducted with K, and the results are shown in Table 7-1.

実施例2 金属試験片とし【銅ン用いる以外は実施例1と同じ試験
を行なった。その結果を表−2に示す。
Example 2 The same test as in Example 1 was conducted except that copper was used as a metal test piece. The results are shown in Table-2.

実施例6 金属試験片として鉄を用いる以外は実施例1と同じ試験
を行なった。その結果を表−3に示す。
Example 6 The same test as in Example 1 was conducted except that iron was used as the metal test piece. The results are shown in Table-3.

実施例4 11001量ppmの水分と5容量チのエタノールyr
含むフロン132bの混合溶剤に安定剤としてNMMを
混合溶剤に対し2容量係、BTAy同じく100重量p
pm加えたものt試料とし、金属試験片として鉄、亜鉛
、銅7用いて安定性試MY行なった、また、比較のため
安定剤ン加えない混合溶剤を用いた。その結果を表−4
に示す。
Example 4 11001 ppm of water and 5 volumes of ethanol yr
Add NMM as a stabilizer to a mixed solvent containing Freon 132b, and add 2 parts by volume to the mixed solvent, and 100 parts by weight as well as BTAy.
A stability test was conducted using iron, zinc, and copper 7 as metal test pieces, and a mixed solvent with no stabilizer added was used for comparison. Table 4 shows the results.
Shown below.

(以下!p!、白) 表−1 表−2 表−6 表−4(Below! p!, white) Table-1 Table-2 Table-6 Table-4

Claims (1)

【特許請求の範囲】[Claims] N−メチルモルホリン、ベンゾトリアゾール、ニトロメ
タンおよびニトロエタンから選ばれる一種または二種以
上を添加することを特徴とする1,2−ジクロロ−1,
1−ジフルオロエタンの安定化法。
1,2-dichloro-1, characterized in that one or more selected from N-methylmorpholine, benzotriazole, nitromethane and nitroethane is added.
Method for stabilizing 1-difluoroethane.
JP26463584A 1984-12-17 1984-12-17 Stabilization of solvent Granted JPS61143331A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26463584A JPS61143331A (en) 1984-12-17 1984-12-17 Stabilization of solvent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26463584A JPS61143331A (en) 1984-12-17 1984-12-17 Stabilization of solvent

Publications (2)

Publication Number Publication Date
JPS61143331A true JPS61143331A (en) 1986-07-01
JPH0531530B2 JPH0531530B2 (en) 1993-05-12

Family

ID=17406084

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26463584A Granted JPS61143331A (en) 1984-12-17 1984-12-17 Stabilization of solvent

Country Status (1)

Country Link
JP (1) JPS61143331A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0496433A2 (en) 1987-10-22 1992-07-29 The Procter & Gamble Company Photoprotection compositions comprising chelating agents
JP2002241795A (en) * 2001-02-21 2002-08-28 Tosoh Corp Cleaning agent

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5679631A (en) * 1979-11-30 1981-06-30 Daikin Ind Ltd Stabilization of fluorine-containing halogenated hydrocarbon
JPS60116636A (en) * 1983-11-30 1985-06-24 Asahi Glass Co Ltd Stabilization of flon

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5679631A (en) * 1979-11-30 1981-06-30 Daikin Ind Ltd Stabilization of fluorine-containing halogenated hydrocarbon
JPS60116636A (en) * 1983-11-30 1985-06-24 Asahi Glass Co Ltd Stabilization of flon

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0496433A2 (en) 1987-10-22 1992-07-29 The Procter & Gamble Company Photoprotection compositions comprising chelating agents
EP0496434A2 (en) 1987-10-22 1992-07-29 The Procter & Gamble Company Photoprotection compositions comprising chelating agents
JP2002241795A (en) * 2001-02-21 2002-08-28 Tosoh Corp Cleaning agent

Also Published As

Publication number Publication date
JPH0531530B2 (en) 1993-05-12

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