JPH0338535A - Fluorohydrocarbon pseudoazeotropic composition - Google Patents
Fluorohydrocarbon pseudoazeotropic compositionInfo
- Publication number
- JPH0338535A JPH0338535A JP1171266A JP17126689A JPH0338535A JP H0338535 A JPH0338535 A JP H0338535A JP 1171266 A JP1171266 A JP 1171266A JP 17126689 A JP17126689 A JP 17126689A JP H0338535 A JPH0338535 A JP H0338535A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- dichloro
- solvent
- present
- methylene chloride
- 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
- Extraction Or Liquid Replacement (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Manufacturing Of Printed Wiring (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弗素化炭化水素系擬共
沸組成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-based pseudoazeotropic composition that can be used as a CFC substitute and has excellent properties as a solvent and the like.
[従来の技術]
弗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、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(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
Many of them are less toxic and chemically stable, and various types of fluorocarbons with different standard boiling points are available.Using these properties, 1.1.2-trichloro-1, 1.1.2-trichloro-1, 2,2-)-Lifluoroethane (R113) is used, trichloromonofluoromethane (R11) is used as a blowing agent, and dichlorodifluoromethane (R12) is used 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代わり、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. Because it causes a chain reaction with ozone and destroys the ozone layer.
These conventional regulations on the use of fluorocarbons have now been implemented. 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 new fluorocarbon composition 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、1.1−ジクロロ−2,2,2−トリフルオ
ロエタン(R123,沸点27.6℃) 、 1.1−
ジクロロ−1−フルオロエタン(R141b沸点32℃
)。[Means for Solving the Problems] The present invention provides 1.1-dichloro-2,2,2-trifluoroethane (R123, boiling point 27.6°C), 1.1-
Dichloro-1-fluoroethane (R141b boiling point 32℃
).
及びメチレンクロライド(沸点39.8℃)とからなる
弗素化炭化水素系層共沸組成物に関するものである。本
発明の組成物は擬共沸組成が存在し、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。and methylene chloride (boiling point 39.8°C). The composition of the present invention has a quasi-azeotropic composition and has higher cleaning power than conventional R113 alone as a cleaning solvent.
It is extremely useful as an alternative.
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。Furthermore, there is little change in composition even after recycling, and
It has the advantage that it can be used in the same way as conventional single fluorocarbons and does not require major changes to the conventional technology.
本発明の組成物の混合比はR123が49〜97重量%
、 R141bが2〜49重量%、及びメチレンクロラ
イドが2〜20重量%であり、好ましくはR123が5
5〜75重量%、 8141bが15〜35重量%。The mixing ratio of the composition of the present invention is 49 to 97% by weight of R123.
, R141b is 2 to 49% by weight, and methylene chloride is 2 to 20% by weight, preferably R123 is 5% by weight.
5-75% by weight, 15-35% by weight of 8141b.
及びメチレンクロライドが5〜15重量%である。and methylene chloride in an amount of 5 to 15% 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。Other components may be further added to the composition of the present invention depending on the intended use. For example, pentane in its application as a solvent.
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,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、
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、1,1.2−トリクロロ−
2,2−ジフルオロエタン(R122)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。Isopentane, hexane, isohexane, neohexane, heptane, isohexane, 2,3-dimethylbutane,
Hydrocarbons such as cyclopentane, nitroalkanes such as nitromethane, nitroethane, nitropropane, amines such as diethylamine, triethylamine, isopropylamine, butylamine, isobutylamine, methanol, ethanol, n-propyl alcohol, i-propyl alcohol, Alcohols such as n-butyl alcohol, i-butyl alcohol, S-butyl alcohol, t-butyl alcohol, ethers such as methyl cellosolve, tetrahydrofuran, 4-dioxane, ketones such as acetone, methyl ethyl ketone, methyl butyl ketone, acetic acid Esters such as ethyl, propyl acetate, butyl acetate,
trans-1,2-dichloroethylene, cis-1
, 2-dichloroethylene, halogenated hydrocarbons such as 2-bromopropane, others, 1,1,2-trichloro-
Fluorocarbons other than those of the present invention, such as 2,2-difluoroethane (R122), etc. can be added as appropriate.
本発明の弗素化炭化水素系層共沸組成物は、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。The fluorinated hydrocarbon layered azeotropic composition of the present invention can be used in various applications such as heat carriers and blowing agents, similar to conventional fluorocarbons, and has higher dissolving power than conventional R113, especially when used as a solvent. Therefore, it is suitable.
溶剤の具体的な用途としては、フラックス。A specific use of the solvent is flux.
グリース、油、ワックス、インキ等の除去剤。Remover for grease, oil, wax, ink, etc.
塗料用溶剤、抽出剤、ガラス、セラミックス。Paint solvents, extractants, glass, and ceramics.
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。Various products made of plastic, rubber, and metal, especially IC parts,
Examples include cleaning agents and draining agents for electrical equipment, precision machinery, optical lenses, etc. Cleaning methods include hand wiping,
Dipping, spraying, 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
本発明の組成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、本発明の組成物に5分間浸漬した。比較例とし
てR113についても同様の試験を行なった。Example 1 A flux cleaning test was conducted using the composition of the present invention. Flux (Tamura AL-4.
Tamura Manufacturing Co., Ltd.) was applied, baked for 2 minutes in an electric furnace at 200°C, and then immersed in the composition of the present invention for 5 minutes. A similar test was also conducted for R113 as a comparative example.
本発明の組成物の混合比及びフラックスの除去の度合い
を第1表に示す。Table 1 shows the mixing ratio of the composition of the present invention and the degree of flux removal.
第
1
表
0:良好に除去できる ○:はぼ良好△:微量残存
×:かなり残存実施例2
本発明の組成物を用いて機械油の洗浄試験を行なった。Table 1 0: Can be removed well ○: Good △: Trace amount remains
×: Significant residual Example 2 A machine oil cleaning test was conducted using the composition of the present invention.
5O3−304のテストピース(25mm+X 30m
mX 2mm厚)を機械油(CQ−30,日本石油■製
〉中に浸漬した後、本発明の組成物中に5分間浸漬した
。比較例としてR113についても同様の試験を行なっ
た。5O3-304 test piece (25mm+X 30m
2 mm thick) was immersed in machine oil (CQ-30, manufactured by Nippon Oil Corporation) for 5 minutes, and then immersed in the composition of the present invention for 5 minutes.As a comparative example, R113 was also subjected to a similar test.
本発明の組成物の混合比及び機械油の除去の度合いを第
2表に示す。The mixing ratio of the composition of the present invention and the degree of removal of machine oil are shown in Table 2.
第2表
0:良好に除去できる ○:はぼ良好△:微量残存
×:かなり残存[発明の効果]
本発明の弗素化炭化水素系擬共沸組成物は、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、従来のフロンと同様の使い
方ができるため、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R1
13に代わる洗浄溶剤として最適である。Table 2 0: Can be removed well ○: Good △: Trace amount remains
×: Significant residual [Effect of the invention] The fluorinated hydrocarbon-based pseudoazeotropic composition of the present invention can be used as an alternative to conventional fluorocarbons while satisfying the excellent properties of conventional fluorocarbons. Since it can be used in the same way as , it has the advantage that it does not require major changes to the conventional technology. In addition, R113, which is often used as a solvent,
R1 has better ability to dissolve and remove flux and oil than R1.
It is most suitable as a cleaning solvent in place of 13.
Claims (2)
タン,1,1−ジクロロ−1−フルオロエタン及びメチ
レンクロライドからなる弗素化炭化水素系擬共沸組成物
。(1) A fluorinated hydrocarbon-based pseudoazeotropic composition consisting of 1,1-dichloro-2,2,2-trifluoroethane, 1,1-dichloro-1-fluoroethane, and methylene chloride.
タン49〜97重量%,1,1−ジクロロ−1−フルオ
ロエタン2〜49重量%,及びメチレンクロライド2〜
20重量%からなる請求項1に記載の組成物。(2) 49-97% by weight of 1,1-dichloro-2,2,2-trifluoroethane, 2-49% by weight of 1,1-dichloro-1-fluoroethane, and 2-49% of methylene chloride
Composition according to claim 1, consisting of 20% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1171266A JPH0338535A (en) | 1989-07-04 | 1989-07-04 | Fluorohydrocarbon pseudoazeotropic composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1171266A JPH0338535A (en) | 1989-07-04 | 1989-07-04 | Fluorohydrocarbon pseudoazeotropic composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0338535A true JPH0338535A (en) | 1991-02-19 |
Family
ID=15920142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1171266A Pending JPH0338535A (en) | 1989-07-04 | 1989-07-04 | Fluorohydrocarbon pseudoazeotropic composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0338535A (en) |
-
1989
- 1989-07-04 JP JP1171266A patent/JPH0338535A/en active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2734624B2 (en) | Fluorinated hydrocarbon-based azeotropic compositions | |
| JPH0327328A (en) | Fluorinated hydrocarbon-based solvent composition | |
| JP2734623B2 (en) | Fluorinated hydrocarbon-based azeotropic compositions | |
| JP2737250B2 (en) | Fluorinated hydrocarbon pseudoazeotrope | |
| JP2737249B2 (en) | Fluorinated hydrocarbon pseudoazeotrope | |
| JPH0338535A (en) | Fluorohydrocarbon pseudoazeotropic composition | |
| JPH0327329A (en) | Fluorinated hydrocarbon-based solvent composition | |
| JPH02207033A (en) | Azeotropic mixture and pseudo-azeotropic mixture of dichloropentafluoropropane | |
| JPH02135296A (en) | Fluorinated hydrocarbon-based azeotropic mixture | |
| JPH0317033A (en) | Fluorinated hydrocarbon-based solvent composition | |
| JPH0331224A (en) | Fluorohydrocarbon azeotropic or pseudoazeotropic composition | |
| JPH02204455A (en) | 1,3-dichloro-1,1,2,2,3-pentafluoropropane-based azeotrope and azeotrope-like composition | |
| JPH02204449A (en) | 1,1-dichloro-2,2,3,3,3-pentafluoropropane-based azeotrope and azeotrope-like composition | |
| JP2738034B2 (en) | Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions | |
| JPH0338533A (en) | Fluorohydrocarbon azeotropic and pseudoazeotropic compositions | |
| JPH0317031A (en) | Fluorinated hydrocarbon-based solvent composition | |
| JPH0374338A (en) | Fluorinated hydrocarbon based azeotropic composition | |
| JPH01141993A (en) | Fluorinated hydrocarbon-based azeotropic mixture | |
| JPH0317029A (en) | Fluorinated hydrocarbon-based solvent composition | |
| JPH0331223A (en) | Fluorohydrocarbon azeotropic or pseudoazeotropic composition | |
| JPH02207031A (en) | Azeotropic composition and pseudo-azeotropic composition of dichloropentafluoropropane | |
| JPH0331222A (en) | Fluorohydrocarbon azeotropic or pseudoazeotropic composition | |
| JPH02202840A (en) | 1-chloro-2,2,3,3-tetrafluoropropane azeotropic and pseudo-azeotropic composition | |
| JPH0331225A (en) | Fluorohydrocarbon azeotropic or pseudoazeotropic composition | |
| JPH02204448A (en) | 1-chloro-2,2,3,3-tetrafluoropropane-based azeotrope and azeotrope-like composition |