JPH02202840A - 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and pseudo-azeotropic composition - Google Patents
1-chloro-2,2,3,3-tetrafluoropropane azeotropic and pseudo-azeotropic compositionInfo
- Publication number
- JPH02202840A JPH02202840A JP1022536A JP2253689A JPH02202840A JP H02202840 A JPH02202840 A JP H02202840A JP 1022536 A JP1022536 A JP 1022536A JP 2253689 A JP2253689 A JP 2253689A JP H02202840 A JPH02202840 A JP H02202840A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- azeotropic
- tetrafluoropropane
- chloro
- dichloro
- 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
沸及び擬共沸組成物に関するものである。[Detailed Description of the Invention] [Industrial Field of Application] The present invention relates to a novel fluorinated hydrocarbon azeotropic and near-azeotropic composition that can be used as a CFC substitute and has excellent properties as a solvent, etc. be.
[従来の技術]
フッ素化炭化水素系化合pIJ(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 pIJ (hereinafter simply referred to as fluorocarbons) are mostly non-toxic, nonflammable, and chemically stable.
Since various types of CFCs with different standard boiling points are available, taking advantage of these properties, 1,1,2-trichloro-1,2,2 can be used as a solvent, blowing agent, propellant, refrigerant, etc.
-trifluoroethane (R113), trichloromonofluoromethane (R11) as a blowing agent, and dichlorodifluoromethane (R12) as a propellant or refrigerant.
[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 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1,2−ジクロロ−1,
1−ジフルオロエタン(R132b)からなるフッ素化
炭化水素系共沸及び擬共沸組成物に関するものである。[Means for Solving the Problems] The present invention provides 1-chloro-2,2,3,3-tetrafluoropropane (R244ca) and 1,2-dichloro-1,
This invention relates to fluorinated hydrocarbon azeotropic and near-azeotropic compositions consisting of 1-difluoroethane (R132b).
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。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。本発明の組成物と
してはR244caが18〜58重量%及びR132b
が42〜82重量%、好ましくは、R244caが28
〜48重量%及びR132bが52〜72重量%であり
、さらに好ましくはR244caの約38重量%とR1
32bの約62重量%からなる共沸組成物である。Furthermore, it has the advantage that there is little change in composition even after recycling, and it can be used in the same way as conventional single fluorocarbons, without requiring major changes to the conventional technology. The composition of the present invention contains 18 to 58% by weight of R244ca and R132b.
is 42 to 82% by weight, preferably R244ca is 28% by weight.
~48 wt.% and R132b is 52-72 wt.%, more preferably about 38 wt.% of R244ca and R132b.
32b.
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、テトラしドロフ
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、=4=
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、酢酸ブチル等のエステル類、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 composition of the present invention depending on the intended use. For example, when used as a solvent, pentane, isopentane, hexane, isohexane, neohexane, heptane, isohexane,
, 3-dimethylbutane, hydrocarbons such as cyclopentane, nitroalkanes such as nitromethane, nitroethane, 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, tetra Hydrofuran, ethers such as 1,4-dioxane, acetone,
Methyl ethyl ketone, = 4 = Ketones such as methyl butyl ketone, esters such as ethyl acetate, propyl acetate, butyl acetate, dichloromethane,
trans-1,2-dichloroethylene, cis-1,
Halogenated hydrocarbons such as 2-dichloroethylene and 2-bromopropane, and fluorocarbons other than those of the present invention such as 1,1-dichloro-1-fluoroethane can be added as appropriate.
R244ca及びR132bからなる本発明の共沸及び
擬共沸組成物は、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、プラスデック、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 azeotropic and near-azeotropic compositions of the present invention consisting of R244ca and R132b can be used in various applications such as heat carriers and blowing agents, similar to conventional fluorocarbons, and especially when used as solvents,
It is suitable because it has higher dissolving power than conventional R113. Specific uses of solvents include removers for flux, grease, oil, wax, and ink, paint solvents, extractants, glass, ceramics, plastic deck, rubber, various metal products, especially IC parts, and electrical equipment. , cleaning agents for precision machinery, optical lenses, etc., and draining agents.
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] 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℃)42
R132b (沸点46.8℃)58その結果、44
℃において留分400gを得た。(Composition) (Weight%) R244ca
(Boiling point 54℃) 42 R132b (Boiling point 46.8℃) 58 As a result, 44
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
38R132b
62実施例 2
本発明の組成物(R244ca/R132b=38重量
%/62重量%)を用いて機械油の洗浄試験を行なった
。(Composition) (Weight%) R244ca
38R132b
62 Example 2 A machine oil cleaning test was conducted using the composition of the present invention (R244ca/R132b=38% by weight/62% by weight).
5US−304のテストピース(25mmX 30m+
nX 2mm厚)を機械油(日本石油製CQ−30)中
に浸漬した後、本発明の前記組成物に5分間浸漬した。5US-304 test piece (25mm x 30m+
nX 2 mm thick) was immersed in machine oil (Nippon Oil Co., Ltd. CQ-30) and then immersed in the composition of the present invention for 5 minutes.
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。As a result, it was confirmed that machine oil could be removed as well as R113.
実施例 3
実施例2の組成物(R244ca/R132b=38重
量%/62重量%)についてタグ式測定法(J Is−
に2265 )に従って測定したところ引火点がなく不
燃であることが確認された。Example 3 The composition of Example 2 (R244ca/R132b=38% by weight/62% by weight) was subjected to tag measurement method (J Is-
2265), 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.
又、溶剤としてよく使われているR113単体よりも、
フラックスや油等の溶解除去性に優れるためR113に
替わる洗浄溶剤として好適である。In addition, compared to R113 alone, which is often used as a solvent,
It is suitable as a cleaning solvent in place of R113 because it has excellent ability to dissolve and remove flux, oil, etc.
−7=−7=
Claims (1)
パン及び1,2−ジクロロ−1,1−ジフルオロエタン
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1,2−ジクロロ−1,1−ジフル
オロエタン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1,2−ジクロロ−1,1−ジフルオロエタン
からなるフッ素化炭化水素系擬共沸組成物。 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1,2−ジクロロ−1,1−
ジフルオロエタン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 1,2-dichloro-1,1-difluoroethane. 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 1,2-dichloro-1,1-difluoroethane. A fluorinated hydrocarbon-based pseudoazeotropic composition consisting of 3,1-chloro-2,2,3,3-tetrafluoropropane and 1,2-dichloro-1,1-difluoroethane. 18-58% by weight of 4,1-chloro-2,2,3,3-tetrafluoropropane and 1,2-dichloro-1,1-
4. A composition according to claim 3, comprising 42 to 82% by weight of difluoroethane.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1022536A JPH02202840A (en) | 1989-02-02 | 1989-02-02 | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and pseudo-azeotropic composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1022536A JPH02202840A (en) | 1989-02-02 | 1989-02-02 | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and pseudo-azeotropic composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02202840A true JPH02202840A (en) | 1990-08-10 |
Family
ID=12085528
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1022536A Pending JPH02202840A (en) | 1989-02-02 | 1989-02-02 | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and pseudo-azeotropic composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02202840A (en) |
-
1989
- 1989-02-02 JP JP1022536A patent/JPH02202840A/en active Pending
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