JP2738034B2 - Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions - Google Patents

Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions

Info

Publication number
JP2738034B2
JP2738034B2 JP1171265A JP17126589A JP2738034B2 JP 2738034 B2 JP2738034 B2 JP 2738034B2 JP 1171265 A JP1171265 A JP 1171265A JP 17126589 A JP17126589 A JP 17126589A JP 2738034 B2 JP2738034 B2 JP 2738034B2
Authority
JP
Japan
Prior art keywords
azeotropic
composition
pseudo
fluorinated hydrocarbon
present
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.)
Expired - Fee Related
Application number
JP1171265A
Other languages
Japanese (ja)
Other versions
JPH0338534A (en
Inventor
昭雄 浅野
徹 上村
直洋 渡辺
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 JP1171265A priority Critical patent/JP2738034B2/en
Publication of JPH0338534A publication Critical patent/JPH0338534A/en
Application granted granted Critical
Publication of JP2738034B2 publication Critical patent/JP2738034B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

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共
沸及び擬共沸組成物に関するものである。
Description: TECHNICAL FIELD The present invention relates to a novel fluorinated hydrocarbon-based azeotropic and pseudo-azeotropic composition which can be used as a substitute for chlorofluorocarbon and has excellent properties as a solvent and the like. is there.

[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−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エ
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 chlorofluorocarbon)
Since many types of fluorocarbons with low toxicity and chemical stability are available, and various types of fluorocarbons having different standard boiling points are available, these characteristics are utilized to make 1,1,2-trichloro- as a solvent, a foaming agent, a propellant or a refrigerant. 1,2,2-Trifluoroethane (R113) is used as a blowing agent, trichloromonofluoroethane (R11) is used, and dichlorodifluoromethane (R12) is used as a propellant and a 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。
[Problems to be Solved by the Invention] R11, R12, and R113, which are chemically particularly stable, have a long life in the troposphere and diffuse to reach the stratosphere, where chlorine radicals generated by decomposition by sunlight are converted into ozone. It causes a chain reaction and destroys the ozone layer, and the use of these conventional fluorocarbons has been regulated. Therefore, instead of these conventional fluorocarbons, the search for alternative fluorocarbons that are less likely to destroy the ozone layer is being actively conducted.

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 novel CFC composition which can be used as an alternative CFC while reducing the amount of conventional CFC used and satisfying the excellent characteristics of the CFC. .

[課題を解決するための手段] 本発明は、1,1−ジクロロ−1−フルオロエタン(R14
1b,沸点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共沸及び擬共沸組成物
に関するものである。本発明の組成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 relates to 1,1-dichloro-1-fluoroethane (R14
1b, boiling point 32 ° C) and methylene chloride (boiling point 39.8
C.) in the form of a fluorinated hydrocarbon-based azeotropic and pseudo-azeotropic composition. Since the composition of the present invention has an azeotropic composition and has a higher detergency than the conventional R113 alone as a cleaning solvent, it is extremely useful as a substitute for R113.

更に、本発明の共沸組成物はリサイクルしても組成の
変動がないこと及び本発明の擬共沸組成物はリサイクル
しても組成の変動が少ないこと,又、本発明の共沸及び
擬共沸組成物は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。
Further, the azeotropic composition of the present invention has no change in composition even when recycled, and the pseudo-azeotropic composition of the present invention has little change in composition even when recycled. The azeotropic composition can be used in the same way as the conventional single CFC,
There are advantages such as not requiring a significant change in the prior art.

本発明の組成物の混合比はR141bが75〜94重量%,及
びメチレンクロライドが6〜25重量%である擬共沸組
成,又はR141bが87.5重量%,及びメチレンクロライド
が12.5重量%である共沸組成である。
The mixing ratio of the composition of the present invention is a pseudo-azeotropic composition in which R141b is 75 to 94% by weight and methylene chloride is 6 to 25% by weight, or a mixture in which R141b is 87.5% by weight and methylene chloride is 12.5% by weight. It is a boiling composition.

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,イソヘプタン,
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、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R141b以外のフロン類等
を適宜添加することができる。
Other components can be further added to and mixed with the composition of the present invention depending on the use. For example, in the use as a solvent, pentane, isopentane, hexane, isohexane, neohexane, heptane, isoheptane,
Hydrocarbons such as 2,3-dimethylbutane and cyclopentane; nitroalkanes such as nitromethane, nitroethane and nitropropane; amines such as diethylamine, triethylamine, isopropylamine, butylamine and isobutylamine; methanol, ethanol and n-propyl Alcohol, i-propyl alcohol, n-butyl alcohol, i-butyl alcohol, s-butyl alcohol, t-
Alcohols such as butyl alcohol; ethers such as methyl cellosolve, tetrahydrofuran and 1,4-dioxane; ketones such as acetone, methyl ethyl ketone and methyl butyl ketone; esters such as ethyl acetate, propyl acetate and butyl acetate; , 2-dichloroethylene, cis
Halogenated hydrocarbons such as -1,2-dichloroethylene, 2-bromopropane, and others, 1,1,2-trichloro-2,2-
Freons other than R141b such as difluoroethane (R122) can be appropriately added.

本発明の弗素化炭化水素系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。
The fluorinated hydrocarbon-based azeotropic and pseudo-azeotropic composition of the present invention,
Like conventional CFCs, it can be used for various applications such as a heating medium and a foaming agent, and is particularly suitable when used as a solvent because it has higher dissolving power than conventional R113.

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 applications of solvents include fluxes, greases, oils, waxes, removers for inks, paint solvents, extractants, glass, ceramics, plastics, rubber, various metallic articles, especially IC parts, electrical equipment, Examples of the cleaning agent include a precision machine, a cleaning agent for an optical lens, and a draining agent.
As a cleaning method, hand wiping, dipping, spraying, rocking, ultrasonic cleaning, steam cleaning, or the like may be employed.

[実施例] 以下に本発明の実施例を示す。[Example] An example of the present invention will be described 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 distillation was performed under atmospheric pressure using a rectification column having 20 theoretical plates.

(組成) (重量%) R141b 90 メチレンクロライド 10 その結果、留出温度27.5℃にて200gの留分を得た。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) (% by weight) R141b 90 Methylene chloride 10 As a result, 200 g of a fraction was obtained at a distillation temperature of 27.5 ° C. This was measured by gas chromatography to find that it had the following composition.

(組成) (重量%) R141b 87.5 メチレンクロライド 12.5 実施例2 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℃で電気炉で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R1
13についても同様の試験を行なった。
(Composition) (% by weight) R141b 87.5 Methylene chloride 12.5 Example 2 A cleaning test of a flux was performed using the composition of the present invention. A flux (Tamura AL-4, manufactured by Tamura Seisakusho) was applied to the entire surface of the printed board, baked in an electric furnace at 200 ° C. for 2 minutes, and immersed in the composition of the present invention for 5 minutes. R1 as a comparative example
A similar test was performed for 13 as well.

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.

実施例3 本発明の組成物を用いて機械油の洗浄試験を行なっ
た。
Example 3 A cleaning test of a machine oil was performed using the composition of the present invention.

SUS−304のテストピース(25mm×30mm×2mm厚)を機
械油(CQ−30,日本石油(株)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。
A test piece (25 mm × 30 mm × 2 mm thick) of SUS-304 was immersed in machine oil (CQ-30, manufactured by Nippon Oil Co., Ltd.), and then immersed in the composition of the present invention for 5 minutes. The same test was performed for R113 as a comparative example.

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。
Table 2 shows the mixing ratio of the composition of the present invention and the degree of removal of the machine oil.

[発明の効果] 本発明の弗素化炭化水素系共沸及び擬共沸組成物は、
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R113に代わる洗浄溶剤として最適である。
[Effect of the Invention] The fluorinated hydrocarbon-based azeotropic and pseudo-azeotropic composition of the present invention comprises:
While satisfying the excellent characteristics of conventional CFCs,
Since it can be used as a substitute for chlorofluorocarbon and can be used in the same manner as conventional chlorofluorocarbon, there is an advantage that a significant change of the conventional technology is not required. In addition, R113 is more suitable as a cleaning solvent instead of R113 because it has better dissolving and removing properties for flux and oil than R113, which is often used as a solvent.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C11D 7/50 C11D 7/50 C23G 5/028 C23G 5/028 5/032 5/032 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C11D 7/50 C11D 7/50 C23G 5/028 C23G 5/028 5/032 5/032

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】1,1−ジクロロ−1−フルオロエタンとメ
チレンクロライドからなる弗素化炭化水素系共沸組成
物。
1. A fluorinated hydrocarbon azeotropic composition comprising 1,1-dichloro-1-fluoroethane and methylene chloride.
【請求項2】1,1−ジクロロ−1−フルオロエタン87.5
重量%,及びメチレンクロライド12.5重量%からなる請
求項1に記載の組成物。
(2) 1,1-dichloro-1-fluoroethane 87.5
The composition according to claim 1, comprising 1% by weight and 12.5% by weight of methylene chloride.
【請求項3】1,1−ジクロロ−1−フルオロエタンとメ
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。
3. A fluorinated hydrocarbon-based pseudo-azeotropic composition comprising 1,1-dichloro-1-fluoroethane and methylene chloride.
【請求項4】1,1−ジクロロ−1−フルオロエタン75〜9
4重量%,及びメチレンクロライド6〜25重量%からな
る請求項3に記載の組成物。
4. A 1,1-dichloro-1-fluoroethane 75 to 9
4. A composition according to claim 3, comprising 4% by weight and 6 to 25% by weight of methylene chloride.
JP1171265A 1989-07-04 1989-07-04 Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions Expired - Fee Related JP2738034B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1171265A JP2738034B2 (en) 1989-07-04 1989-07-04 Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1171265A JP2738034B2 (en) 1989-07-04 1989-07-04 Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions

Publications (2)

Publication Number Publication Date
JPH0338534A JPH0338534A (en) 1991-02-19
JP2738034B2 true JP2738034B2 (en) 1998-04-08

Family

ID=15920123

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1171265A Expired - Fee Related JP2738034B2 (en) 1989-07-04 1989-07-04 Fluorinated hydrocarbon azeotropic and pseudo-azeotropic compositions

Country Status (1)

Country Link
JP (1) JP2738034B2 (en)

Also Published As

Publication number Publication date
JPH0338534A (en) 1991-02-19

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