JPH02202838A - 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like composition - Google Patents
1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like compositionInfo
- Publication number
- JPH02202838A JPH02202838A JP1022534A JP2253489A JPH02202838A JP H02202838 A JPH02202838 A JP H02202838A JP 1022534 A JP1022534 A JP 1022534A JP 2253489 A JP2253489 A JP 2253489A JP H02202838 A JPH02202838 A JP H02202838A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- azeotropic
- dichloromethane
- tetrafluoropropane
- chloro
- 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
Links
Landscapes
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は2代替フロンとして使用て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
沸及び共沸様組成物に関するものである。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a novel fluorinated hydrocarbon azeotrope and azeotrope-like composition that can be used as a substitute for CFCs and has excellent properties as a solvent, etc. It is.
[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)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。[Prior art] Fluorinated hydrocarbon compounds (hereinafter simply referred to as fluorocarbons) are mostly non-toxic, non-flammable, and chemically stable, and various types of fluorocarbons with different standard boiling points are available. 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
内での弁台が長く、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 valve stand in the troposphere and diffuse into the stratosphere, where they are decomposed by sunlight and generate chlorine radicals. Conventional regulations on the use of these fluorocarbons have been implemented because they cause a chain reaction with ozone 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、従来のフロンと同等な種々の優れた特性を有
しており代替フロンとして有用な炭素数が3の新規な含
水素クロロフルオロプロパン系フロンを含む組成物を提
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 composition containing a novel hydrogen-containing chlorofluoropropane-based fluorocarbon with a carbon number of 3, which has various excellent properties equivalent to conventional fluorocarbons and is useful as a fluorocarbon substitute. It is something to do.
[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)及びジクロロメタンからなる
フッ素化炭化水素系共沸及び共沸様組成物に関するもの
である。本発明の組成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単体よ
りも洗浄力が高いため、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 relates to fluorinated hydrocarbon azeotropic and azeotrope-like compositions consisting of 1-chloro-2,2,3,3-tetrafluoropropane (R244ca) and dichloromethane. be. The composition of the present invention is nonflammable, has an azeotropic composition, and has higher detergency as a cleaning solvent than conventional R113 alone, so 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、従来技術の大幅な
変更を要しないこと等の利点がある0本発明の組成物と
してはR244caが18〜58重量%及びジクロロメ
タンが42〜82重量%、重量しくは、R244caが
28〜48重量%及びジクロロメタンが52〜72重量
%であり、さらに好ましくはR244caの約38重量
%とジクロロメタンの約62重量%からなる共沸組成物
である。Furthermore, R244ca is the composition of the present invention, which has the advantage that there is little change in composition even when recycled, and it can be used in the same way as conventional single fluorocarbons, without requiring major changes in conventional technology. 18-58% by weight of R244ca and 42-82% by weight of dichloromethane, more preferably about 38% by weight of R244ca and about 62% by weight of dichloromethane. It is an azeotropic composition consisting of % by weight.
本発明の組成物には、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、インペンタン、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、シクロペンクン等の炭化水素類
、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、酢酸プロビル、酢酸ブチル等のエステル
類、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 composition of the present invention depending on the intended use. For example, when used as a solvent, pentane, impentane, hexane, isohexane, neohexane, heptane, isohexane,
.. Hydrocarbons such as 3-dimethylbutane and cyclopenkune, nitroalkanes such as nitromethane, nitroethane and nitropropane, diethylamine, triethylamine,
Amines such as isopropylamine, butylamine, isobutylamine, alcohols such as methanol, ethanol, n-propyl alcohol, i-propyl alcohol, n-butanol, i-butanol, S-butanol, t-butanol, methyl cellosolve, tetrahydrofuran , ethers such as 1,4-dioxane, acetone,
Ketones such as methyl ethyl ketone and methyl butyl ketone, esters such as ethyl acetate, proyl acetate, butyl acetate, trans-1,2-dichloroethylene, cis-
Halogenated hydrocarbons such as 1,2-dichloroethylene and 2-bromopropane, others, 1,1-dichloro-1-
Fluorocarbons other than those of the present invention, such as fluoroethane, can be added as appropriate.
R244’ca及びジクロロメタンからなる本発明の共
沸及び共沸様組成物は、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より高い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。洗浄方法としては、手拭き、浸漬、スプレ揺動、
超音波洗浄、蒸気洗浄等を採用すればよい。The azeotrope and azeotrope-like composition of the present invention, which consists of R244'ca and dichloromethane, can be used in various applications such as heat carriers and blowing agents, similar to conventional fluorocarbons, and especially when used as a solvent, it has a higher level of performance than conventional R113. It is suitable because it has high 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. Cleaning methods include hand wiping, soaking, spray shaking,
Ultrasonic cleaning, steam cleaning, etc. may be used.
[実施例] 以下に本発明の実施例を示す。[Example] Examples of the present invention are shown below.
実施例 1
下記の組成からなる溶剤組成物1000g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 composition having the composition shown below 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℃)50
ジクロロメタン(沸点39.8℃)50その結果、35
℃において留分400gを得た。(Composition) (Weight%) R244ca
(Boiling point 54℃) 50 Dichloromethane (Boiling point 39.8℃) 50 As a result, 35
400 g of fraction were obtained at .degree.
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
38ジクロロメ
タン 62
実施例 2
本発明の組成物(R244ca/ジクロロメタン・38
重重量/62重量%)を用いてフラックスの洗浄試験を
行なった。(Composition) (Weight%) R244ca
38 dichloromethane 62 Example 2 Composition of the present invention (R244ca/dichloromethane/38
A flux cleaning test was conducted using 62% by weight).
プリント基板全面にフラックス(クムラ製作所製りAラ
−AL−4)を塗布し、200℃の電気炉で2分間焼成
後、本発明の前記組成物に1分間浸漬した。その結果、
フラックスは良好に除去てきることが確認された。Flux (AL-AL-4 manufactured by Kumura Manufacturing Co., Ltd.) was applied to the entire surface of the printed circuit board, and after baking it in an electric furnace at 200° C. for 2 minutes, it was immersed in the composition of the present invention for 1 minute. the result,
It was confirmed that flux could be removed well.
実施例 3
実施例2の組成物(R244ca/ジクロロメタン・3
8重重量/62重量%)についてタグ式測定法(JTS
−に2265 )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J忍された。Example 3 Composition of Example 2 (R244ca/dichloromethane.3
8wt/62wt%) using the tag-type measurement method (JTS
-2265), it was confirmed that it had no flash point and was non-flammable.
[発明の効果]
本発明のフッ素化炭化水素系組成物は、不燃性で従来の
フロン類が有している優れた特性と同等以上の特性を有
する。又、共沸点が存在するため、リサイクル時に組成
変動がなく、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必要とせず、そのまま適用できる等
の利点がある。[Effects of the Invention] The fluorinated hydrocarbon composition of the present invention is nonflammable and has properties equivalent to or superior to those of conventional fluorocarbons. Furthermore, since it has an azeotropic point, there is no change in composition during recycling, and it can be used in the same way as conventional single chlorofluorocarbons, which has the advantage of being able to be applied as is without requiring major changes to the conventional technology.
Claims (1)
パン及びジクロロメタンからなるフッ素化炭化水素系共
沸組成物。 2、1−クロロ−2,2,3,3−テトラフルオロプロ
パン38重量%及びジクロロメタン62重量%からなる
請求項1に記載の組成物。 3、1−クロロ−2,2,3,3−テトラフルオロプロ
パン及びジクロロメタンからなるフッ素化炭化水素系共
沸様組成物。 4、1−クロロ−2,2,3,3−テトラフルオロプロ
パン18〜58重量%及びジクロロメタン42〜82重
量%からなる請求項3に記載の組成物。[Scope of Claims] A fluorinated hydrocarbon azeotropic composition comprising 1,1-chloro-2,2,3,3-tetrafluoropropane and dichloromethane. A composition according to claim 1, consisting of 38% by weight of 2,1-chloro-2,2,3,3-tetrafluoropropane and 62% by weight of dichloromethane. A fluorinated hydrocarbon azeotrope-like composition comprising 3,1-chloro-2,2,3,3-tetrafluoropropane and dichloromethane. 4. A composition according to claim 3, consisting of 18-58% by weight of 4,1-chloro-2,2,3,3-tetrafluoropropane and 42-82% by weight of dichloromethane.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1022534A JPH02202838A (en) | 1989-02-02 | 1989-02-02 | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1022534A JPH02202838A (en) | 1989-02-02 | 1989-02-02 | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02202838A true JPH02202838A (en) | 1990-08-10 |
Family
ID=12085468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1022534A Pending JPH02202838A (en) | 1989-02-02 | 1989-02-02 | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and azeotropic-like composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02202838A (en) |
-
1989
- 1989-02-02 JP JP1022534A patent/JPH02202838A/en active Pending
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