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JPH0531530B2 - - Google Patents
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JPH0531530B2 - - Google Patents

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Publication number
JPH0531530B2
JPH0531530B2 JP59264635A JP26463584A JPH0531530B2 JP H0531530 B2 JPH0531530 B2 JP H0531530B2 JP 59264635 A JP59264635 A JP 59264635A JP 26463584 A JP26463584 A JP 26463584A JP H0531530 B2 JPH0531530 B2 JP H0531530B2
Authority
JP
Japan
Prior art keywords
freon
conducted
present
stability
zinc
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.)
Expired - Lifetime
Application number
JP59264635A
Other languages
Japanese (ja)
Other versions
JPS61143331A (en
Inventor
Megumi Furuno
Nobuaki Imamori
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

Links

Landscapes

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

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、1,2−ジクロロ−1,1−ジフル
オロエタン(以下、フロン132bと称する)の安
定化法に関する。 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
コーンウエハーやシリコンチツプ等の半導体材
料、ICやLSI等の半導体類、プリント配線基板、
リレースイツチ、マイクロモーター等の電子・電
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に有用であ
る。 (従来の技術) フロン132bは現実には未だ産業界で実用的に
は用いられず、その特性については未知な部分が
多い。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つた分
解挙動を示すため、その安定化には未だ充分な方
法が知られていない。 (発明が解決しようとする問題点) フロン132b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の塩素系溶
剤に較べて安定性が高く、一般の使用条件下では
安定化は必らずしも必要ではないが、それでも水
分が共存する場合とか、電子機器や精密機器類の
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
ている銅、亜鉛、鉄等の金属材料の存在下で溶剤
の劣化が起きるときは、同時にこれらの金属の腐
蝕をひき起すことになり、被洗物の品質に悪影響
を与える。 (問題点を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を重ねた結果、その方法を見
出し本発明に到達した。 すなわち、本発明は、N−メチルホルモリンお
よびニトロメタンから選ばれる一種または二種と
ベンゾトリアゾール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
チルホルモリン、ニトロメタン、については溶剤
に対し5容量%以下、ベンゾトリアゾールについ
ては溶剤に対し3000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
なつて析出したり、引火性が生じたりして得策で
はない。また、本発明の方法はフロン132bを主
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132bの溶剤特性を著しく変えない範囲
において、メタノール、エタノール、イソプロパ
ノール、イソブタノール、tert−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
ンクロライド等をフロン132bに少量部加えた混
合溶剤についてもその適用が可能である。 (発明の効果) 本発明によつ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、鉄等の金属材料を腐蝕させることが少
ないので、各分野における洗浄剤として幅広く使
用することができる。 (実施例) 以下に本発明を実施例によつて説明する。 なお、実施例における安定性試験は次の方法に
よつて行なわれた。また安定剤は次の略号で示
す。 N−メチルモルホリン:NMM ニトロメタン:NM ベンゾトリアゾール:BTA 安定性試験:試料50mlを容量100mlのガラスびん
に入れ、これに充分によく磨いた亜鉛、銅、鉄
等の金属試験片を、その下半分が液相部につか
るように入れて密閉し、60℃で96時間処理す
る。金属片の腐蝕状態を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 水分を800重量ppm含むフロン132bおよび表−
1に示す各種安定剤を加えたものと安定剤を加え
ないものを試料とし、金属試験片として亜鉛を用
いて安定性試験を行なつた。また、比較のため安
定剤を加えないフロン132bについても安定性試
験を行つた。その結果を表−1に示す。 実施例 2 金属試験片として銅を用いる以外は実施例1と
同じ試験を行なつた。その結果を表−2に示す。 実施例 3 金属試験片として鉄を用いる以外は実施例1と
同じ試験を行なつた。その結果を表−3に示す。 実施例 4 1100重量ppmの水分と5容量%のエタノールを
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%、BTAを同じく100重
量ppm加えたものを試料とし、金属試験片として
鉄、亜鉛、銅を用いて安定性試験を行なつた。ま
た、比較のため安定剤を加えない混合溶剤を用い
た。その結果を表−4に示す。
(Industrial Application Field) The present invention relates to a method for stabilizing 1,2-dichloro-1,1-difluoroethane (hereinafter referred to as Freon 132b). Freon 132b is nonflammable, has low toxicity, and has excellent solubility and an appropriate boiling point, so it can be used as a cleaning agent for various articles. For example, semiconductor materials such as silicone wafers and silicon chips, semiconductors such as ICs and LSIs, printed wiring boards,
Electronic and electrical equipment such as relay switches, micro motors, watches, cameras, micro bearings,
Useful as a degreasing agent for precision instruments such as lenses. (Prior Art) Freon 132b has not yet been practically used in industry, and many aspects of its properties are unknown. Among them, it exhibits a decomposition behavior different from conventional chlorine-based solvents and fluorine-based solvents that do not contain fluorine atoms or hydrogen atoms, so no sufficient method for stabilizing it is known yet. (Problems to be solved by the invention) Freon 132b is more stable than chlorinated solvents such as methyl chloroform, tetrachlorethylene, and trichlorethylene, and stabilization is not necessarily required under general usage conditions. However, its stability may still be a problem when moisture coexists or when quality requirements are high and strict, such as when cleaning electronic equipment or precision equipment. In particular, when solvents deteriorate in the presence of metal materials such as copper, zinc, and iron, which are often used in electronic/electrical equipment and precision equipment, it will also cause corrosion of these metals, and the adversely affect the quality of products. (Means for Solving the Problems) The present inventors have conducted various studies in an attempt to improve the stability of Freon 132b, and as a result, they have found a method and arrived at the present invention. That is, the present invention is a method for stabilizing 1,2-dichloro-1,1-difluoroethane, which is characterized by adding one or two selected from N-methylformoline and nitromethane and benzotriazole. Although the amount of stabilizer added in the present invention is not particularly limited, it is usually 5% by volume or less for N-methylformoline and nitromethane, and 3000 ppm by weight or less for benzotriazole based on the solvent. 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 132b as a main component. In other words, mixed solvents in which a small amount of methanol, ethanol, isopropanol, isobutanol, tert-butanol, acetone, methyl ethiketone, ethyl acetate, methylene chloride, etc. are added to Freon 132b may be used as long as the solvent properties of Freon 132b are not significantly changed. Its application is possible. (Effects of the Invention) Freon 132b stabilized by the present invention and its mixed solvent have extremely high chemical stability;
Since it rarely corrodes metal materials such as copper, zinc, and iron, it can be widely used as a cleaning agent in various fields. (Example) The present invention will be explained below using examples. In addition, the stability test in Examples was conducted by the following method. Stabilizers are indicated by the following abbreviations. N-Methylmorpholine: NMM Nitromethane: NM Benzotriazole: BTA Stability test: Place 50 ml of the sample in a 100 ml glass bottle, and place a well-polished metal test piece of zinc, copper, iron, etc. in the lower half of the bottle. Pour the tube so that it touches the liquid phase, seal it, and treat it at 60℃ for 96 hours. The corrosion state of the metal piece is observed separately in the part exposed to the gas phase and the part immersed in the liquid phase. Example 1 Freon 132b containing 800 ppm of water and Table-
A stability test was conducted using zinc as a metal test piece, using samples with and without the addition of the various stabilizers shown in 1. For comparison, a stability test was also conducted on Freon 132b without any stabilizer added. The results are shown in Table-1. Example 2 The same test as in Example 1 was conducted except that copper was used as the metal test piece. The results are shown in Table-2. Example 3 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. Example 4 NMM was added as a stabilizer to a mixed solvent of Freon 132b containing 1100 ppm by weight of water and 5% by volume of ethanol.
A stability test was conducted using iron, zinc, and copper as metal test pieces, using a sample containing 2% by volume of BTA and 100 ppm by weight of BTA in a mixed solvent. For comparison, a mixed solvent without any stabilizer was used. The results are shown in Table 4.

【表】【table】

【表】【table】

【表】【table】

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 N−メチルモルホリンおよびニトロメタンか
ら選ばれる一種または二種とベンゾトリアゾール
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- characterized in that one or two selected from N-methylmorpholine and nitromethane and benzotriazole are added.
Method for stabilizing 1,1-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 JPS61143331A (en) 1986-07-01
JPH0531530B2 true 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)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3856315T2 (en) 1987-10-22 1999-10-14 The Procter & Gamble Co. Sunscreen containing chelating agents
JP2002241795A (en) * 2001-02-21 2002-08-28 Tosoh Corp Washing soap

Family Cites Families (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

Also Published As

Publication number Publication date
JPS61143331A (en) 1986-07-01

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