JPH02202836A - 1,3-dichloro-1,1,2,2,3-pentafluoropropane azeotropic and azeotropic-line mixture - Google Patents
1,3-dichloro-1,1,2,2,3-pentafluoropropane azeotropic and azeotropic-line mixtureInfo
- Publication number
- JPH02202836A JPH02202836A JP1022532A JP2253289A JPH02202836A JP H02202836 A JPH02202836 A JP H02202836A JP 1022532 A JP1022532 A JP 1022532A JP 2253289 A JP2253289 A JP 2253289A JP H02202836 A JPH02202836 A JP H02202836A
- Authority
- JP
- Japan
- Prior art keywords
- mixture
- azeotropic
- dichloro
- pentafluoropropane
- r225cb
- 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]
本発明は7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 7 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, nonflammable, and chemically stable, and various fluorocarbons with different standard boiling points are available, so they can be used to take advantage of these characteristics. 1.1.2-Trichloro-1,2,2-trifluoroethane (R113) is used as a solvent, blowing agent, propellant, or refrigerant, and trichloromonofluoromethane (R11) is used as a blowing agent. 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=1
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 = 1 chlorine radicals are generated by decomposition by sunlight. Conventional regulations on the use of these fluorocarbons have been implemented because they are believed to 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1.3−ジクロロ−1,1,2,2,3−ペン
タフルオロプロパン(R225cb)及び1,1.2−
)シクロロー1.2.2g、i、jノルオロエタン(R
113)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。[Means for Solving the Problems] The present invention provides 1,3-dichloro-1,1,2,2,3-pentafluoropropane (R225cb) and 1,1,2-
) Cycloro 1.2.2g, i, j noroloethane (R
113) of fluorinated hydrocarbon azeotropes and azeotrope-like mixtures.
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。The mixture of the present invention is nonflammable, has an azeotropic composition, and has the same cleaning power as conventional R113 alone as a cleaning solvent, 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。本発明の混合物と
してはR225cbが12〜52重量%及びR113が
48〜88重景%、重量しくは、R225cbが22〜
42重量%及びR113が58〜78重量%であり、さ
らに好ましくはR225cbの約32重量%とR113
の約68重量%からなる共沸混合物である。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 mixture of the present invention contains 12 to 52% by weight of R225cb and 48 to 88% by weight of R113, specifically, 22 to 52% by weight of R225cb.
42% by weight of R113 and 58-78% by weight, more preferably about 32% by weight of R225cb and R113.
It is an azeotrope consisting of about 68% by weight of
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、シクロベ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、メチルエ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 mixture 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 cyclobencune, 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, tetrahydrofuran , ethers such as 1,4-dioxane, acetone,
Ketones such as methyl ethyl ketone and methyl ethyl ketone, esters such as ethyl acetate, propyl acetate and butyl acetate, halogenated hydrocarbons such as dichloromethane, trans-1,2-dichloroethylene, cis-1,2-dichloroethylene and 2-bromopropane , Others, 1.1
-Dichloro-1-fluoroethane and other fluorocarbons other than those of the present invention can be added as appropriate.
R225cb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 R225cb 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 medium and blowing agent. 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] 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%)R225cb
(沸点55.4℃)30R113(沸点47.6℃)
70
その結果、46℃において留分380gを得た。(Composition) (% by weight) R225cb
(boiling point 55.4℃) 30R113 (boiling point 47.6℃)
70 As a result, 380 g of a fraction was obtained at 46°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%)R225cb
32R11368
実施例 2
本発明の混合物(R225cb/R113=32重景%
/68重量%)を用いて機械油の洗浄試験を行なった。(Composition) (% by weight) R225cb
32R11368 Example 2 Mixture of the present invention (R225cb/R113=32%
/68% by weight) 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 2 mm 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.
実施例 3
実施例2の混合物(R225cb/R113=32重量
%/68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 (R225cb/R113 = 32% by weight/68% by weight) was tested using the tag method (JIS-2).
265), it was confirmed that it had no flash point and was nonflammable.
[発明の効果コ
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=7
Claims (1)
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、1,3−ジクロロ−1,1,2,2,3−ペンタフ
ルオロプロパン32重量%及び1,1,2−トリクロロ
−1,2,2−トリフルオロエタン68重量%からなる
請求項1に記載の混合物。 3、1,3−ジクロロ−1,1,2,2,3−ペンタフ
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、1,3−ジクロロ−1,1,2,2,3−ペンタフ
ルオロプロパン12〜52重量%及び1,1,2−トリ
クロロ−1,2,2−トリフルオロエタン48〜88重
量%からなる請求項3に記載の混合物。[Claims] 1,1,3-dichloro-1,1,2,2,3-pentafluoropropane and 1,1,2-trichloro-1,2,
A fluorinated hydrocarbon azeotrope consisting of 2-trifluoroethane. Claim 1 consisting of 32% by weight of 2,1,3-dichloro-1,1,2,2,3-pentafluoropropane and 68% by weight of 1,1,2-trichloro-1,2,2-trifluoroethane. The mixture described in. 3,1,3-dichloro-1,1,2,2,3-pentafluoropropane and 1,1,2-trichloro-1,2,
A fluorinated hydrocarbon azeotrope-like mixture consisting of 2-trifluoroethane. From 12 to 52% by weight of 4,1,3-dichloro-1,1,2,2,3-pentafluoropropane and from 48 to 88% by weight of 1,1,2-trichloro-1,2,2-trifluoroethane 4. The mixture according to claim 3.
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1022532A JPH02202836A (en) | 1989-02-02 | 1989-02-02 | 1,3-dichloro-1,1,2,2,3-pentafluoropropane azeotropic and azeotropic-line mixture |
DK90102015.6T DK0381216T3 (en) | 1989-02-01 | 1990-02-01 | Azeotrope or azeotrope-like chlorofluorocarbon hydride mixture |
DE69024378T DE69024378T2 (en) | 1989-02-01 | 1990-02-01 | Azeotropic or azeotrope-like composition based on chlorofluorocarbons |
PCT/JP1990/000119 WO1990008814A1 (en) | 1989-02-01 | 1990-02-01 | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
AU50345/90A AU623748B2 (en) | 1989-02-01 | 1990-02-01 | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
KR1019900702196A KR970002043B1 (en) | 1989-02-01 | 1990-02-01 | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
ES90102015T ES2083978T3 (en) | 1989-02-01 | 1990-02-01 | AZEOTROPIC MIXTURE OR SIMILAR TO AN AZEOTROPIC MIXTURE BASED ON HYDROGENATED, CHLORINATED AND FLUORATED HYDROCARBONS. |
AT90102015T ATE132182T1 (en) | 1989-02-01 | 1990-02-01 | AZEOTROPIC OR AZEOTROP-LIKE COMPOSITION BASED ON CHLOROFLUOROHYDROCARBONS |
EP90102015A EP0381216B1 (en) | 1989-02-01 | 1990-02-01 | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
US07/942,328 US5607912A (en) | 1989-02-01 | 1992-09-09 | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
GR960400809T GR3019425T3 (en) | 1989-02-01 | 1996-03-26 | Hydrochlorofluorocarbon azeotropic or azeotropic-like mixture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1022532A JPH02202836A (en) | 1989-02-02 | 1989-02-02 | 1,3-dichloro-1,1,2,2,3-pentafluoropropane azeotropic and azeotropic-line mixture |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02202836A true JPH02202836A (en) | 1990-08-10 |
Family
ID=12085412
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1022532A Pending JPH02202836A (en) | 1989-02-01 | 1989-02-02 | 1,3-dichloro-1,1,2,2,3-pentafluoropropane azeotropic and azeotropic-line mixture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02202836A (en) |
-
1989
- 1989-02-02 JP JP1022532A patent/JPH02202836A/en active Pending
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