JPH02209835A - Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane - Google Patents

Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane

Info

Publication number
JPH02209835A
JPH02209835A JP1029652A JP2965289A JPH02209835A JP H02209835 A JPH02209835 A JP H02209835A JP 1029652 A JP1029652 A JP 1029652A JP 2965289 A JP2965289 A JP 2965289A JP H02209835 A JPH02209835 A JP H02209835A
Authority
JP
Japan
Prior art keywords
mixture
dichloroethylene
tetrafluoropropane
chloro
weight
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
JP1029652A
Other languages
Japanese (ja)
Inventor
Shunichi Samejima
鮫島 俊一
Tateo Kitamura
健郎 北村
Naohiro Watanabe
渡辺 直洋
Akio Asano
浅野 昭雄
Toru Kamimura
徹 上村
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 JP1029652A priority Critical patent/JPH02209835A/en
Publication of JPH02209835A publication Critical patent/JPH02209835A/en
Pending legal-status Critical Current

Links

Landscapes

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

Abstract

PURPOSE:To obtain the subject mixture having excellent characteristics comparable or superior to those of conventional fluorocarbons and suitable as a fluorocarbon substitute by using R244ca, R225ca and trans-1,2-dichloroethylene as essential components. CONSTITUTION:The objective azeotropic mixture is composed of (A) 11wt.% of 1-chloro-2,2,3,3-tetrafluoropropane (R244ca), (B) 47wt.% of 1,1-dichloro-2,2,3,3,3- pentafluoropropane (R225ca) and (C) 42wt.% of trans-1,2-dichloroethylene and the azeotrope-like mixture is composed of 3-69wt.% of A, 8-78wt.% of B and 3-54wt.% of C, preferably 6-36wt.% of A, 42-72wt.% of B and 5-47wt.% of C. The mixture has azeotropic point, causes little variation of composition in recycling and can be used in similar manner as conventional simple fluorocarbon. It has higher dissolving power than conventional R113 when used especially as a solvent.

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)は
、毒性が少なく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5 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−)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(R1−1)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 often less toxic and chemically stable, and various types of fluorocarbons with different standard boiling points are available. 1.1.2-Trichloro-1,2,2-)lifluoroethane (R113) is used as a blowing agent, propellant, or refrigerant, and trichloromonofluoromethane (R1-1) is used as a blowing agent, propellant, or refrigerant. Dichlorodifluoromethane (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旧1、R12、R113は対流圏内
での鍔命が長く、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や
 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] Old 1, R12, and R113, which are particularly chemically stable, have a long life in the troposphere and diffuse into the stratosphere, where they are decomposed by sunlight and generate chlorine radicals. Regulations on the use of these conventional fluorocarbons have been implemented because they are said to cause a chain reaction with ozone and destroy the ozone layer. The search for alternative CFCs is actively underway.

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 mixture 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 an alternative fluorocarbon. It is something.

〔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)、1.1−ジクロロ−2,2
,3,3,3−ペンタフルオロプロパン(R225ca
)、及びtrans−1,2−ジクロロエチレンからな
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0本発明の混合物は共沸組成が存在し、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 provides 1-chloro-2,2,3,3-tetrafluoropropane (R244Ca), 1,1-dichloro-2,2
,3,3,3-pentafluoropropane (R225ca
), and trans-1,2-dichloroethylene. The mixture of the present invention has an azeotropic composition, and is particularly useful as a cleaning solvent when compared to conventional R113 alone. Because of its high detergency, 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かある。
Furthermore, 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 to the conventional technology.

本発明の混合物としてはR244caが3〜69重量%
、R225caが8〜78重景%重景びtrans−1
,2−ジクロロエチレンが3〜54重景%重景ましくは
、R244caが6〜36重景%重景225caが42
〜72重景%、重景trans−1゜2〜ジクロロエチ
レンが5〜47重量%である0本発明の共沸組成は、R
244caの約11重量%、 R225caの約47重
量%及び、trans−1,2−ジクロロエチレンの約
42重量%である。
The mixture of the present invention contains 3 to 69% by weight of R244ca.
, R225ca is 8-78% heavy view and trans-1
, 2-dichloroethylene is 3 to 54% heavy, or R244ca is 6 to 36% heavy, 225ca is 42
The azeotropic composition of the present invention is R
244ca, about 47% by weight of R225ca, and about 42% by weight of trans-1,2-dichloroethylene.

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0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−ブチルアル
コール、i−ブチルアルコール、S−ブチルアルコール
、t−ブチルアルコ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、
酢酸ブチル等のエステル類、ジクロロメタン、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 application.
, 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-butyl alcohol, i-butyl alcohol, S-butyl alcohol, t-butyl alcohol, Ethers such as methyl cellosolve, tetrahydrofuran, 1,4-dioxane, ketones such as acetone, methyl ethyl ketone, methyl butyl ketone, ethyl acetate, propyl acetate,
Esters such as butyl acetate, dichloromethane, 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.

R244ca、  R225ca及び、trans−1
,2−ジクロロエチレン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より高い溶解力を有するため好適である。
R244ca, R225ca and trans-1
, 2-dichloroethylene, the azeotrope and azeotrope-like mixture of the present invention can be used in various applications such as heat carriers and blowing agents, similar to conventional fluorocarbons, and especially when used as a solvent, has a higher solubility than conventional R113. It is suitable because it has power.

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、スプレー 揺動、超音
波洗浄、蒸気洗浄等を採用すればよい。
Specific uses of solvents include flux, grease,
Removers for oil, wax, ink, etc., paint solvents, extractants, cleaning agents and draining agents for glass, ceramics, plastics, rubber, various metal products, especially IC parts, electrical equipment, precision machinery, optical lenses, etc. can be mentioned. 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混合物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 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℃)10 R225ca (沸点51.3℃)50trans−1
,2−ジクロロエチレン   40(沸点47.7℃) その結果、留分390gを得た。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。
(Composition) (Weight%) R244ca
(Boiling point 54℃) 10 R225ca (Boiling point 51.3℃) 50trans-1
,2-dichloroethylene 40 (boiling point 47.7°C) As a result, 390 g of a fraction was obtained. As a result of measuring this product with a gas chromatograph, it had the following composition.

(組成)          (重量%)R244ca
            11R225ca     
       47trans−1,2−ジクロロエヂ
レン 42実施例 2 本発明の混合物(R244ca、/R,225ea/1
rans−1,2−ジクロロエチレン−11重量%/4
7重量%/42重景%)を用いて機械油の洗浄試験を行
なった。
(Composition) (Weight%) R244ca
11R225ca
47 trans-1,2-dichloroethylene 42 Example 2 Mixture of the present invention (R244ca, /R,225ea/1
rans-1,2-dichloroethylene-11% by weight/4
A machine oil cleaning test was conducted using 7% by weight/42% by weight).

5O3−304のテストピース(25+wmX 30m
mX 2++n厚)を81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。
5O3-304 test piece (25+wmX 30m
mX 2++n thickness) with 81 machine oil (Nippon Oil CQ-30
> immersed in the mixture of the invention for 5 minutes. As a result, it was confirmed that machine oil could be removed as well as R113.

実施例 3 実施例2の混合物(R244ca/R225ca/1r
ans−1,2−ジクロロエチレン=11重量%/47
重量%/42重量%)を用いてフラックスの洗浄試験を
行なった。
Example 3 Mixture of Example 2 (R244ca/R225ca/1r
ans-1,2-dichloroethylene = 11% by weight/47
A flux cleaning test was conducted using a flux (% by weight/42% by weight).

プリント基板全面にフラックス(タムシ製作所製りAr
−AL−4)を塗布し、200℃の電気炉で2分間焼成
後、本発明の前記混合物に1分間浸漬した。その結果、
フラックスは良好に除去できることが確認された。
Flux (Ar manufactured by Tamushi Seisakusho) is applied to the entire printed circuit board.
-AL-4) was applied, baked for 2 minutes in an electric furnace at 200°C, and then immersed in the mixture of the present invention for 1 minute. the result,
It was confirmed that flux could be removed well.

[発明の効果] 本発明のフッ素化炭化水素系混合物は、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、リサイクル時に組成変動が少なく
、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 mixture of the present invention has properties equivalent to or superior to those of conventional fluorocarbons. It also has the advantage of having an azeotropic point, having little compositional variation during recycling, and can be used in the same way as conventional single fluorocarbons, and can be applied as is without requiring major changes to conventional technology.

代理人(弁理士)  半−h 不リナAgent (patent attorney) Half-h Furina

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、1,1−ジクロロ−2,2,3,3,3−ペンタ
フルオロプロパン、及びtrans−1,2−ジクロロ
エチレ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11重量%、1,1−ジクロロ−2,2,3,3,
3−ペンタフルオロプロパン47重量%、及びtran
s−1,2−ジクロロエチレン42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、1,1−ジクロロ−2,2,3,3,3−ペンタ
フルオロプロパン、及びtrans−1,2−ジクロロ
エチレ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3〜69重量%、1,1−ジクロロ−2,2,3,
3,3−ペンタフルオロプロパン8〜78重量%、及び
trans−1,2−ジクロロエチレン3〜54重量%
からなる請求項3に記載の混合物。
[Claims] 1,1-chloro-2,2,3,3-tetrafluoropropane, 1,1-dichloro-2,2,3,3,3-pentafluoropropane, and trans-1,2 -A fluorinated hydrocarbon azeotrope consisting of dichloroethylene. 2,1-chloro-2,2,3,3-tetrafluoropropane 11% by weight, 1,1-dichloro-2,2,3,3,
47% by weight of 3-pentafluoropropane, and tran
A mixture according to claim 1, consisting of 42% by weight of s-1,2-dichloroethylene. Fluorination consisting of 3,1-chloro-2,2,3,3-tetrafluoropropane, 1,1-dichloro-2,2,3,3,3-pentafluoropropane, and trans-1,2-dichloroethylene Hydrocarbon azeotrope-like mixture. 4,1-chloro-2,2,3,3-tetrafluoropropane 3-69% by weight, 1,1-dichloro-2,2,3,
3,3-pentafluoropropane 8-78% by weight, and trans-1,2-dichloroethylene 3-54% by weight
A mixture according to claim 3 consisting of.
JP1029652A 1989-02-10 1989-02-10 Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane Pending JPH02209835A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1029652A JPH02209835A (en) 1989-02-10 1989-02-10 Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1029652A JPH02209835A (en) 1989-02-10 1989-02-10 Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane

Publications (1)

Publication Number Publication Date
JPH02209835A true JPH02209835A (en) 1990-08-21

Family

ID=12282040

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1029652A Pending JPH02209835A (en) 1989-02-10 1989-02-10 Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane

Country Status (1)

Country Link
JP (1) JPH02209835A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07167786A (en) * 1993-06-29 1995-07-04 Boehringer Mannheim Gmbh Method of detecting and evaluating analog optical measurement signals in a test carrier analysis system

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07167786A (en) * 1993-06-29 1995-07-04 Boehringer Mannheim Gmbh Method of detecting and evaluating analog optical measurement signals in a test carrier analysis system

Similar Documents

Publication Publication Date Title
JPH02209835A (en) Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane
JPH02207033A (en) Azeotropic mixture and pseudo-azeotropic mixture of dichloropentafluoropropane
JPH02207032A (en) Azeotropic mixture and azeotrope-like mixture of dichloropentafluoropropane
JPH0331224A (en) Fluorohydrocarbon azeotropic or pseudoazeotropic composition
JPH02204455A (en) 1,3-dichloro-1,1,2,2,3-pentafluoropropane-based azeotrope and azeotrope-like composition
JPH02207031A (en) Azeotropic composition and pseudo-azeotropic composition of dichloropentafluoropropane
JPH02209828A (en) Azeotropic and azeotrope-like mixture of chlorotetrafluoropropane
JP2692230B2 (en) Fluorinated hydrocarbon azeotropes and azeotrope-like compositions
JPH0374338A (en) Fluorinated hydrocarbon based azeotropic composition
JP2737260B2 (en) Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions
JPH02207051A (en) 1-chloro-2,2,3,3-tetrafluoropropane-based azeotrope or azeotrope-like mixture
JPH02209831A (en) Azeotropic mixture and pseudo-azeotropic mixture of chlorotetrafluoropropane
JPH02202833A (en) 1,3-dichloro-1,1,2,2,3-pentafluoropropane based azeotropic and azeotropic like composition
JPH02209837A (en) Azeotropic composition and pseudo-azeotropic composition of 1-chloro-2,2,3,3-tetrafluoropropane
JPH02212440A (en) Azeotropic and azeotrope-like composition of chlorotetrafluoropropane
JPH02204451A (en) 1,3-dichloro-1,1,2,2,3-pentafluoropropane-based azeotrope and pseudo azeotrope
JPH02204447A (en) 1,1-dichloro-2,2,3,3,3-pentafluoropropane-based azeotrope and pseudo azeotrope composition
JPH02207047A (en) 1,1-dichloro-2,2,3,3,3-pentafluoropropane-based azeotropic or azeotropic-like mixture
JPH02207034A (en) Azeotropic and pseudo-azeotropic mixture of dichloropentafluoropropane
JPH02204465A (en) 1,-chloro-2,2,3,3-tetrafluoropropane based azeotropic and pseudo-azeotropic mixture
JPH02209830A (en) Azeotropic mixture and azeotrope-like mixture of chlorotetrafluoropropane
JPH02204459A (en) 1,1-dichloro-2,2,3,3,3-pentafluoropropane based azeotropic and pseudo-azeotropic mixture
JPH0399030A (en) Fluorinated hydrocarbon based-azeotropic composition
JPH02204463A (en) 1,1,-dichloro-2,2,3,3,3-pentafluoropropane based azeotropic and pseudo-azeotropic mixture
JPH02207030A (en) Azeotropic composition and azeotrope-like composition of dichloropentafluoropropane