JPH01141996A - Fluorinated hydrocarbon-based azeotropic mixture - Google Patents
Fluorinated hydrocarbon-based azeotropic mixtureInfo
- Publication number
- JPH01141996A JPH01141996A JP30008587A JP30008587A JPH01141996A JP H01141996 A JPH01141996 A JP H01141996A JP 30008587 A JP30008587 A JP 30008587A JP 30008587 A JP30008587 A JP 30008587A JP H01141996 A JPH01141996 A JP H01141996A
- Authority
- JP
- Japan
- Prior art keywords
- mixture
- fluorocarbon
- dimethylbutane
- methylbutane
- pentane
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5036—Azeotropic mixtures containing halogenated solvents
- C11D7/5068—Mixtures of halogenated and non-halogenated solvents
- C11D7/5072—Mixtures of only hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/028—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons
- C23G5/02809—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons containing chlorine and fluorine
- C23G5/02825—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons containing chlorine and fluorine containing hydrogen
- C23G5/02829—Ethanes
- C23G5/02832—C2H3Cl2F
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Extraction Or Liquid Replacement (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、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-like mixture that can be used as a CFC substitute and has excellent properties as a solvent and the like.
[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
れらの特性を生かして溶剤、発泡剤、プロペラントある
いは冷媒等として種々のフロンが使われている。例えば
、溶剤として1,1.2− トリクロロ−1,2,2−
トリフルオロエタン(RI+3)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(RI21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.
Since various types of fluorocarbons with different standard boiling points are available, they are used as solvents, blowing agents, propellants, refrigerants, etc. by taking advantage of these characteristics. For example, 1,1,2-trichloro-1,2,2-
Trifluoroethane (RI+3) is used as a blowing agent, trichloromonofluoromethane (R11) is used as a blowing agent, and dichlorodifluoromethane (RI21) is used as a propellant or refrigerant.
[発明の解決しようとする問題点]
化学的に特に安定なR11,RI2.RII3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を規制する動きがある。このた
め、これらの従来のフロンに替わり、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。[Problems to be solved by the invention] Chemically particularly stable R11, RI2. RII3 has a long life in the troposphere and diffuses into the stratosphere, where it is decomposed by sunlight and generates chlorine radicals that cause a chain reaction with ozone and destroy the ozone layer. There is a movement to regulate the use of For this reason, the search for alternative fluorocarbons that are less likely to deplete the ozone layer is being actively conducted in place of these conventional fluorocarbons.
本発明は、従来の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 novel fluorocarbon mixture that can be used as a fluorocarbon substitute while satisfying the excellent properties of conventional fluorocarbons.
[問題点を解決するための手段]
本2発明は炭化水素類の1種と1,1−ジクロロ−1−
フルオ゛ロエタン(RI41b) とからなるフッ素化
炭化水、素糸共沸様混合物に関するものである。[Means for Solving the Problems] The second invention provides a combination of one kind of hydrocarbons and 1,1-dichloro-1-
The present invention relates to a fluorinated hydrocarbon and an azeotrope-like mixture of fluoroethane (RI41b) and fluoroethane (RI41b).
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RI 1’3よりも洗浄力が高いため、 RI
+3の代替として極めて有用なものである。RI
This is an extremely useful alternative to +3.
更に、リサイクルしても組成の変動が少なく、従来の単
一フロンと同じ使い方ができるため、従来技術の大幅な
変更を要しないこと等の利点があげられる。Furthermore, even after recycling, there is little change in composition, and it can be used in the same way as conventional single fluorocarbons, so it has the advantage of not requiring major changes to conventional technology.
本発明の各炭化水素類のR141bに対する混合比はn
−ペンタンは15〜35重量%、2−メチルブタンは3
8〜58重量%、2,2−ジメチルブタンは1〜21重
量%であり、好ましくはn−ペンタンが20〜30重量
%、2−メチルブタンが43〜53重量%、2.2−ジ
メチルブタンが5〜15重量%であり、さらに好ましく
はn−ペンタンが25.5重量%、2−メチルブタンが
48.5重量%、2.2−ジメチルブタンが10重量%
である。The mixing ratio of each hydrocarbon of the present invention to R141b is n
- Pentane is 15-35% by weight, 2-methylbutane is 3% by weight.
8 to 58% by weight, 2,2-dimethylbutane is 1 to 21% by weight, preferably n-pentane is 20 to 30% by weight, 2-methylbutane is 43 to 53% by weight, and 2,2-dimethylbutane is 1 to 21% by weight. 5 to 15% by weight, more preferably 25.5% by weight of n-pentane, 48.5% by weight of 2-methylbutane, and 10% by weight of 2.2-dimethylbutane.
It is.
本発明の混合物には、用途に応じてその他の成分をさら
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、ヘキサン、イソヘキサン、ヘプタン、イ
ソへブ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、1−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、酢酸ブチル等のエステル類等
から選ばれる1種又は2種以上を添加混合することがで
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, hydrocarbons such as hexane, isohexane, heptane, and isohebutane, nitroalkanes such as nitromethane, nitroethane, and nitropropane, diethylamine, triethylamine, isopropylamine, butylamine, isobutylamine, etc. Amines, alcohols such as methanol, ethanol, n-propyl alcohol, i-propyl alcohol, n-butanol, 1-butanol, ethers such as methyl cellosolve, tetrahydrofuran, 1,4-dioxane, acetone, methyl ethyl ketone, methyl One or more selected from ketones such as butyl ketone, esters such as ethyl acetate, propyl acetate, butyl acetate, etc. can be added and mixed. .
RI41b及び炭化水素類からなる本発明の混合物は、
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RI+3に
比べ溶解力が高いため好適である。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J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。The mixture of the invention consisting of RI41b and hydrocarbons is
Like conventional fluorocarbons, it can be used for various purposes such as a heat medium and a blowing agent, and is particularly suitable when used as a solvent because it has higher dissolving power than conventional RI+3. Specific uses of solvents include removal agents for flux, grease, oil, wax, ink, etc., solvents for paints, extractants, glass, ceramics, plastics, rubber, various metal products, especially ICs.
Examples include cleaning agents and draining agents for parts, electrical equipment, precision machinery, optical lenses, etc. As a cleaning method, hand wiping, dipping, spraying, shaking, ultrasonic cleaning, steam cleaning, etc. may be used.
[実施例]
実施例1
第1表に示した各組成からなる混合物1.000gを各
々、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い、各々400gの留分を得
た。この時の各留出温度は第2表の通りであった。又、
′この留分をガスクロマトグラフで測定した結果、第2
表の通りであった。[Example] Example 1 1.000 g of each mixture having the composition shown in Table 1 was placed in a distillation flask, and distilled under atmospheric pressure using a rectification column with 20 theoretical plates. A fraction was obtained. The distillation temperatures at this time were as shown in Table 2. or,
'As a result of measuring this fraction with a gas chromatograph, the second
It was as shown in the table.
第1表
第2表
実施例2
本発明の混合物を用いてフラックスの洗浄試験を行なっ
た。プリント基板全面にフラックス(タムラーAL−4
.タムラ製作所製)を塗布し、200℃の電気炉で2分
間焼成後、本発明の混合物に1分間浸漬した。比鮫例と
してR113についても同様の試験を行なった。本発明
の混合物組成とフラックスの除去の度合を第3表に示す
。Table 1 Table 2 Example 2 A flux cleaning test was conducted using the mixture of the present invention. Flux (Tamler AL-4) on the entire printed circuit board
.. (manufactured by Tamura Seisakusho) 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. A similar test was conducted for R113 as an example of a shark. Table 3 shows the composition of the mixture of the present invention and the degree of flux removal.
第 3 表
0:完全に除去、 O:微量残存
△;少量残存、 X:かなり残存
[発明の効果]
本発明のフッ素化炭化水素系共沸様混合物は、従来のフ
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
じ使い方ができ、従来技術の大幅な変更を要しない等の
利点がある。又、溶剤としてよく使われているR113
よりもフラックスや油等の溶解除去性に優れるため旧1
3に替わる洗浄溶剤として好適である。Table 3: 0: completely removed, O: trace amount remaining △; small amount remaining, It can be used as a substitute for CFCs while satisfying the above characteristics, and since it has an azeotropic point,
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. In addition, R113, which is often used as a solvent,
Old 1 because it has better ability to dissolve and remove flux and oil, etc.
It is suitable as a cleaning solvent in place of No. 3.
Claims (1)
メチルブタンから選ばれる1種と1,1−ジクロロ−1
−フルオロエタンとからなるフッ素化炭化水素系共沸様
混合物。One selected from 1, n-pentane, 2-methylbutane, or 2,2-dimethylbutane and 1,1-dichloro-1
- a fluorinated hydrocarbon azeotrope-like mixture consisting of fluoroethane.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30008587A JPH01141996A (en) | 1987-11-30 | 1987-11-30 | Fluorinated hydrocarbon-based azeotropic mixture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP30008587A JPH01141996A (en) | 1987-11-30 | 1987-11-30 | Fluorinated hydrocarbon-based azeotropic mixture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01141996A true JPH01141996A (en) | 1989-06-02 |
Family
ID=17880522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP30008587A Pending JPH01141996A (en) | 1987-11-30 | 1987-11-30 | Fluorinated hydrocarbon-based azeotropic mixture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01141996A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5057547A (en) * | 1990-04-06 | 1991-10-15 | Mobay Corporation | Rigid foams using blends of chlorofluorocarbons and hydrocarbons as blowing agent |
| US5085798A (en) * | 1990-09-11 | 1992-02-04 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane, cyclopentane and optionally an alkanol |
| US5102920A (en) * | 1991-04-06 | 1992-04-07 | Mobay Corporation | Novel azeotropes and the use thereof in the production of rigid foams |
| US5106527A (en) * | 1990-04-06 | 1992-04-21 | Mobay Corporation | Azeotropes of 2-methylbutane and 1,1-dichloro-1-fluorethane and the use thereof in the production of rigid foams |
| US5419849A (en) * | 1993-06-18 | 1995-05-30 | Fields; Paul B. | Cleaning fluids |
| US5454969A (en) * | 1993-06-18 | 1995-10-03 | Fields; Paul B. | Cleaning fluids |
| US5472989A (en) * | 1995-03-24 | 1995-12-05 | Bayer Corporation | Aezotropic compositions of 1,1,1,4,4,4-hexafluorobutane and n-pentane and the use thereof in the production of foams |
| US5532283A (en) * | 1995-03-24 | 1996-07-02 | Bayer Corporation | Azeotropic compositions of 1,1,1,4,4,4-hexafluorobutane and 2-methyl butane and the use thereof in the production of foams |
| US5562857A (en) * | 1995-12-22 | 1996-10-08 | Bayer Corporation | Azeotrope-like compositions of 1,1,1,3,3-pentafluoropropane and 2-methyl butane |
| US5614565A (en) * | 1995-03-24 | 1997-03-25 | Bayer Corporation | Azeotropic compositions of perfluorohexane and hydrocarbons having 6 carbon atoms and the use thereof in the production of foams |
| US5716541A (en) * | 1996-09-23 | 1998-02-10 | Bayer Corporation | Azeotrope-like compositions of 1,1,1,3,3 pentafluoropropane and tetramethylsilane |
| US6358908B1 (en) | 1995-03-24 | 2002-03-19 | Bayer Corporation | Azeotropic compositions of 1,3-dioxolane and hydrocarbons having 5 or 6 carbon atoms and the use thereof in the production of foams |
| US6372705B1 (en) | 1995-03-24 | 2002-04-16 | Bayer Corporation | Azeotropic compositions of perfluorohexane and hydrocarbons having 5 carbon atoms and the use thereof in the production of foams |
-
1987
- 1987-11-30 JP JP30008587A patent/JPH01141996A/en active Pending
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5057547A (en) * | 1990-04-06 | 1991-10-15 | Mobay Corporation | Rigid foams using blends of chlorofluorocarbons and hydrocarbons as blowing agent |
| US5106527A (en) * | 1990-04-06 | 1992-04-21 | Mobay Corporation | Azeotropes of 2-methylbutane and 1,1-dichloro-1-fluorethane and the use thereof in the production of rigid foams |
| US5085798A (en) * | 1990-09-11 | 1992-02-04 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane, cyclopentane and optionally an alkanol |
| US5102920A (en) * | 1991-04-06 | 1992-04-07 | Mobay Corporation | Novel azeotropes and the use thereof in the production of rigid foams |
| US5419849A (en) * | 1993-06-18 | 1995-05-30 | Fields; Paul B. | Cleaning fluids |
| US5454969A (en) * | 1993-06-18 | 1995-10-03 | Fields; Paul B. | Cleaning fluids |
| US5532283A (en) * | 1995-03-24 | 1996-07-02 | Bayer Corporation | Azeotropic compositions of 1,1,1,4,4,4-hexafluorobutane and 2-methyl butane and the use thereof in the production of foams |
| US5488073A (en) * | 1995-03-24 | 1996-01-30 | Bayer Corporation | Azeotropic compositions of 1,1,1,4,4,4-hexafluorobutane and N-pentane and the use thereof in the production of foams |
| US5472989A (en) * | 1995-03-24 | 1995-12-05 | Bayer Corporation | Aezotropic compositions of 1,1,1,4,4,4-hexafluorobutane and n-pentane and the use thereof in the production of foams |
| US5574072A (en) * | 1995-03-24 | 1996-11-12 | Bayer Corporation | Azeotropic compositions of 1,1,1,4,4,4-hexafuorobutane and n-pentane and the use thereof in the production of foams |
| US5614565A (en) * | 1995-03-24 | 1997-03-25 | Bayer Corporation | Azeotropic compositions of perfluorohexane and hydrocarbons having 6 carbon atoms and the use thereof in the production of foams |
| US6358908B1 (en) | 1995-03-24 | 2002-03-19 | Bayer Corporation | Azeotropic compositions of 1,3-dioxolane and hydrocarbons having 5 or 6 carbon atoms and the use thereof in the production of foams |
| US6372705B1 (en) | 1995-03-24 | 2002-04-16 | Bayer Corporation | Azeotropic compositions of perfluorohexane and hydrocarbons having 5 carbon atoms and the use thereof in the production of foams |
| US5562857A (en) * | 1995-12-22 | 1996-10-08 | Bayer Corporation | Azeotrope-like compositions of 1,1,1,3,3-pentafluoropropane and 2-methyl butane |
| US5716541A (en) * | 1996-09-23 | 1998-02-10 | Bayer Corporation | Azeotrope-like compositions of 1,1,1,3,3 pentafluoropropane and tetramethylsilane |
| US5854296A (en) * | 1996-09-23 | 1998-12-29 | Bayer Corporation | Azeotrope-like compositions of 1,1,1,3,3-pentafluoropropane and tetramethylsilane |
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