JPH02202841A - 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like mixture - Google Patents

1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like mixture

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Publication number
JPH02202841A
JPH02202841A JP1022537A JP2253789A JPH02202841A JP H02202841 A JPH02202841 A JP H02202841A JP 1022537 A JP1022537 A JP 1022537A JP 2253789 A JP2253789 A JP 2253789A JP H02202841 A JPH02202841 A JP H02202841A
Authority
JP
Japan
Prior art keywords
tetrafluoropropane
mixture
azeotropic
chloro
composition
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
JP1022537A
Other languages
Japanese (ja)
Inventor
Akio Asano
浅野 昭雄
Naohiro Watanabe
渡辺 直洋
Shunichi Samejima
鮫島 俊一
Tateo Kitamura
健郎 北村
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.)
AGC Inc
Original Assignee
Asahi Glass 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 Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP1022537A priority Critical patent/JPH02202841A/en
Publication of JPH02202841A publication Critical patent/JPH02202841A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To provide the subject nonflammable composition enabling to reduce the using amount of CFCs and useful as an alternate CFC by comprising 1- chloro-2,2,3,3-tetrafluoropropane and 1,1,2-trichloro-1,2,2-trifluoroethane. CONSTITUTION:A composition comprises 6-46wt.%, especially preferably 26wt.%, of 1-chloro-2,2,3,3-tetrafluoropropane and 54-94wt.%, especially preferably 74wt.%, of 1,1,2-trichloro-1,2,2-trifluoroethane (R113). The composition is nonflammable, enables to reduce the using amount of the CFCs while satisfying the excellent characteristics of the CFCs, does not cause the change of the composition thereof on the recyclization because of having an azeotropic point, can be used in the same manner as one of the conventional CFCs, does not require the wide change of the conventional techniques and further has other advantages.

Description

【発明の詳細な説明】 「産業上の利用分野] 本発明は1代替フロンとして使用できるとともに溶剤等
として優れた特性を有する新規なフッ素化炭化水素系共
沸及び共沸様混合物に関するものである。
[Detailed Description of the Invention] "Industrial Application Field" The present invention relates to a novel fluorinated hydrocarbon azeotrope and azeotrope-like mixture that can be used as a CFC substitute and has excellent properties as a solvent, etc. .

「従来の技術] フッ素化炭化水素系化合物(以下単にフロンというンは
、毒性が少なく不燃で化学的に安定なものが多く、標準
沸点の異なる各種フロンが入手できることから、これら
の特性を活かして溶剤、発泡剤、プロペラントあるいは
冷媒等として1.1.2トリクロロ−1,2,2−トリ
フルオロエタン(R113)が、発泡剤としてトリクロ
ロモノフルオロメタン(R11)が、プロペラントや冷
媒としてジクロロジフルオロメタン(R12”)が使わ
れている。
``Conventional technology'' Fluorinated hydrocarbon compounds (hereinafter simply referred to as chlorofluorocarbons) are mostly non-toxic, nonflammable, and chemically stable, and various types of fluorocarbons with different standard boiling points are available, making use of these characteristics. 1.1.2 Trichloro-1,2,2-trifluoroethane (R113) is used as a solvent, blowing agent, propellant, or refrigerant, trichloromonofluoromethane (R11) is used as a blowing agent, and dichloro is used as a propellant or refrigerant. Difluoromethane (R12'') is used.

[発明が解決しようとする課題] 化学的に特に安定なR11、R12、R113は対流圏
内での寿命か長く、拡散して成層圏に達し、ここで太陽
光線により分解して発生する塩素ラジカルがオゾンと連
鎖反応を起こし、オゾン層を破壊するとのことから、こ
れら従来のフロンの使用規制が実施されることとなった
。このため、これらの従来のフロンに変わり、オゾン層
を破壊しにくい代替フロンの探索が活発に行なわれてい
る。
[Problem to be solved by the invention] R11, R12, and R113, which are particularly stable chemically, have a long life in the troposphere and diffuse into the stratosphere, where they are decomposed by sunlight and generate chlorine radicals, which are converted into ozone. Conventional regulations on the use of these fluorocarbons have been implemented because they are believed to cause a chain reaction and destroy the ozone layer. For this reason, there is active search for alternative fluorocarbons that are less likely to deplete the ozone layer in place of these conventional fluorocarbons.

本発明は、従来のフロンの使用量を低減し、且つ該フロ
ンが有している優れた特性を満足しながら代替フロンと
して使用できる新規なフロン混合物を提供することを目
的とするものである。
An object of the present invention is to provide a new fluorocarbon mixture that can be used as a fluorocarbon substitute while reducing the amount of conventional fluorocarbons used and satisfying the excellent properties of the fluorocarbons.

[課題を解決するための手段] 本発明は1−クロロ−2,2,3,3−テトラフルオロ
プロパン(R244ca)及び1,1.2−)シクロロ
ー1.2.2− )−リフルオロエタン(R113)か
らなるフッ素化炭化水素系共沸及び共沸様混合物に関す
るものである。本発明の混合物は不燃性であるとともに
共沸組成が存在し、特に洗浄溶剤として従来のR113
単体と洗浄力が同程度であるため、R113代替として
極めて有用なものである。
[Means for Solving the Problems] The present invention provides 1-chloro-2,2,3,3-tetrafluoropropane (R244ca) and 1,1.2-)cyclo-1,2.2-)-lifluoroethane. The present invention relates to fluorinated hydrocarbon azeotropic and azeotrope-like mixtures consisting of (R113). The mixture of the present invention is non-flammable and has an azeotropic composition, in particular the conventional R113 as a cleaning solvent.
Since it has the same detergency as that of the simple substance, it is extremely useful as a substitute for R113.

更に、リサイクルしても組成の変動が少ないこと、又従
来の単一フロンと同じ使い方ができ、従末技術の大幅な
変更を要しないこと等の利点がある。本発明の混合物と
してはR244caが6〜46重量%及びR113が5
4〜94重量%、好ましくは、R244caが16〜3
6重量%及びR113が64〜84重景%で重量、さら
に好ましくはR244caの約26重量%とR113の
約74重量%からなる共沸混合物である。
Further, it has the advantage that there is little change in composition even after recycling, it can be used in the same way as conventional single fluorocarbons, and it does not require major changes in conventional technology. The mixture of the present invention contains 6 to 46% by weight of R244ca and 5% by weight of R113.
4 to 94% by weight, preferably 16 to 3 R244ca
6% by weight and R113 by weight of 64-84%, more preferably an azeotrope consisting of about 26% by weight of R244ca and about 74% by weight of R113.

本発明の混合物には、用途に応じてその他の成分を更に
添加混合することができる。例えば、溶剤としての用途
においては、ペンタン、イ、ソペンタン、ヘキサン、イ
ソヘキサン、ネオヘキサン、ヘプタン、イソへブタン、
2.3−ジメチルブタン、シクロペンタン等の炭化水素
類、ニトロメタン、ニトロエタン、ニトロプロパン等の
ニトロアルカン類、ジエチルアミン、トリエチルアミン
、イソプロピルアミン、ブチルアミン、イソブチルアミ
ン等のアミン類、メタノール、エタノール、n −プロ
ピルアルコール、i−プロピルアルコール、n−ブタノ
ール、i−ブタノール、S−ブタノール、t−ブタノー
ル等のアルコール類、メチルセロソルブ、テトラヒドロ
フラン、1,4−ジオキサン等のエーテル類、アセトン
、メチルエチルケトン、メチルブチルケトン等のケトン
類、酢酸エチル、酢酸プロピル、酢酸ブチル等のニスデ
ル類、ジクロロメタン、trans−1,2−ジクロロ
エチレン、cis−1,2−ジクロロエチレン、2−ブ
ロモプロパン等のハロゲン化炭化水素類、その他、1,
1−ジクロロ−1−フルオロエタン等の本発明以外のフ
ロン類等を適宜添加することができる。
Other components may be further added to the mixture of the present invention depending on the intended use. For example, when used as a solvent, pentane, i, sopentane, hexane, isohexane, neohexane, heptane, isohexane,
2. Hydrocarbons such as 3-dimethylbutane and cyclopentane, nitroalkanes such as nitromethane, nitroethane, and nitropropane, amines such as diethylamine, triethylamine, isopropylamine, butylamine, and isobutylamine, methanol, ethanol, n-propyl Alcohol, alcohols such as i-propyl alcohol, n-butanol, i-butanol, S-butanol, t-butanol, ethers such as methyl cellosolve, tetrahydrofuran, 1,4-dioxane, acetone, methyl ethyl ketone, methyl butyl ketone, etc. Ketones, Nisdels such as ethyl acetate, propyl acetate, butyl acetate, halogenated hydrocarbons such as dichloromethane, trans-1,2-dichloroethylene, cis-1,2-dichloroethylene, 2-bromopropane, etc., 1 ,
Fluorocarbons other than those of the present invention, such as 1-dichloro-1-fluoroethane, etc. can be added as appropriate.

R244ca及びR113からなる本発明の共沸及び共
沸様混合物は、従来のフロンと同様、熱媒体や発泡剤等
の各種用途に使用でき、特に溶剤として用いた場合、従
来のR113と同程度の溶解力を有するため好適である
。溶剤の具体的な用途としては、フラックス、グリース
、油、ワックス、インキ等の除去剤、塗料用溶剤、抽出
剤、ガラス、セラミックス、プラスチック、ゴム、金属
製各種物品、特にIC部品、電気機器、精密機械、光学
レンズ等の洗浄剤や水切り剤等を挙げることができる。
The azeotrope and azeotrope-like mixture of the present invention consisting of R244ca and R113 can be used for various purposes such as heat carriers and blowing agents, similar to conventional fluorocarbons, and especially when used as a solvent, the azeotrope and azeotrope-like mixture of the present invention can be used for various purposes such as heat transfer media and blowing agents. It is suitable because it has a dissolving power. Specific uses of solvents include removers for flux, grease, oil, wax, and ink, paint solvents, extractants, glass, ceramics, plastics, rubber, various metal products, especially IC parts, electrical equipment, Examples include cleaning agents and draining agents for precision instruments, optical lenses, etc.

洗浄方法としては、手拭き、浸漬、スプレー 揺動、超
音波洗浄、蒸気洗浄等を採用すればよい。
As cleaning methods, hand wiping, dipping, spray shaking, ultrasonic cleaning, steam cleaning, etc. may be used.

[実施例子 以下に本発明の実施例を示す。[Example child Examples of the present invention are shown below.

実施例 1 下記の組成からなる溶剤混合物1000 gを蒸留フラ
スコに入れ、理論段数20段の精留塔を用い、大気圧下
で蒸留を行なった。
Example 1 1000 g of a solvent mixture having the following composition was placed in a distillation flask and distilled under atmospheric pressure using a rectification column with 20 theoretical plates.

(組成)          (重量%)R244ca
 (沸点54°C)20 R113< 4点47.6℃)80 その結果、47℃において留分410gを得た。
(Composition) (Weight%) R244ca
(Boiling point 54°C) 20 R113 < 4 points 47.6°C) 80 As a result, 410 g of a fraction was obtained at 47°C.

このものをガスクロマトグラフで測定した結果、次の組
成であった。
As a result of measuring this product with a gas chromatograph, it had the following composition.

(組成)          (重量%)R244ca
            26R11374 実施例 2 本発明の混合物(R244ca/R113=26重景%
/74重足%)を用いて機械油の洗浄試験を行なった。
(Composition) (Weight%) R244ca
26R11374 Example 2 Mixture of the present invention (R244ca/R113=26%
/74 weight percent) was used to conduct a machine oil cleaning test.

5US−304のテストピース(25mmX 30mm
X 2mm厚)を機械油(日本石油製CQ−30>中に
浸漬した後、本発明の前記混合物に5分間浸漬した。そ
の結果、機械油は、R113と同様、良好に除去できる
ことが確認された。
5US-304 test piece (25mm x 30mm
X 2mm thick) was immersed in machine oil (Nippon Oil Co., Ltd. CQ-30>) and then immersed in the mixture of the present invention for 5 minutes. As a result, it was confirmed that machine oil could be removed as well as R113. Ta.

実施例 3 実施例2の混合物(R244ca/R113=26重量
%/74重量%)についてタグ式測定法(JIS−に2
265 )に従って測定したところ引火点がなく不燃で
あることが確認された。
Example 3 The mixture of Example 2 (R244ca/R113 = 26% by weight/74% by weight) was tested using the tag method (JIS-2).
265), it was confirmed that it had no flash point and was nonflammable.

[発明の効果] 本発明のフッ素化炭化水素系混合物は、不燃性で従来の
フロン類が有している優れた特性を満足しながら該フロ
ンの使用量が低減できるとともに、共沸点が存在するた
め、リサイクル時に組成変動がない、従来の単一フロン
と同じ使い方でき、従来技術の大幅な変更を要しない等
の利点がある。
[Effects of the Invention] The fluorinated hydrocarbon mixture of the present invention is nonflammable and satisfies the excellent properties of conventional fluorocarbons, while reducing the amount of fluorocarbons used, and has an azeotropic point. Therefore, it has the advantage that there is no change in composition during recycling, it can be used in the same way as conventional single fluorocarbons, and it does not require major changes to conventional technology.

7一71

Claims (1)

【特許請求の範囲】 1、1−クロロ−2,2,3,3−テトラフルオロプロ
パン及び1,1,2−トリクロロ−1,2,2−トリフ
ルオロエタンからなるフッ素化炭化水素系共沸混合物。 2、1−クロロ−2,2,3,3−テトラフルオロプロ
パン26重量%及び1,1,2−トリクロロ−1,2,
2−トリフルオロエタン74重量%からなる請求項1に
記載の混合物。 3、1−クロロ−2,2,3,3−テトラフルオロプロ
パン及び1,1,2−トリクロロ−1,2,2−トリフ
ルオロエタンからなるフッ素化炭化水素系共沸様混合物
。 4、1−クロロ−2,2,3,3−テトラフルオロプロ
パン6〜46重量%及び1,1,2−トリクロロ−1,
2,2−トリフルオロエタン54〜94重量%からなる
請求項3に記載の混合物。
[Claims] Fluorinated hydrocarbon azeotrope consisting of 1,1-chloro-2,2,3,3-tetrafluoropropane and 1,1,2-trichloro-1,2,2-trifluoroethane blend. 26% by weight of 2,1-chloro-2,2,3,3-tetrafluoropropane and 1,1,2-trichloro-1,2,
A mixture according to claim 1, consisting of 74% by weight of 2-trifluoroethane. A fluorinated hydrocarbon azeotrope-like mixture consisting of 3,1-chloro-2,2,3,3-tetrafluoropropane and 1,1,2-trichloro-1,2,2-trifluoroethane. 6-46% by weight of 4,1-chloro-2,2,3,3-tetrafluoropropane and 1,1,2-trichloro-1,
A mixture according to claim 3, consisting of 54 to 94% by weight of 2,2-trifluoroethane.
JP1022537A 1989-02-02 1989-02-02 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like mixture Pending JPH02202841A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1022537A JPH02202841A (en) 1989-02-02 1989-02-02 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like mixture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1022537A JPH02202841A (en) 1989-02-02 1989-02-02 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like mixture

Publications (1)

Publication Number Publication Date
JPH02202841A true JPH02202841A (en) 1990-08-10

Family

ID=12085557

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1022537A Pending JPH02202841A (en) 1989-02-02 1989-02-02 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like mixture

Country Status (1)

Country Link
JP (1) JPH02202841A (en)

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