JPH02215737A - Fluorinated hydrocarbon-based mixed composition - Google Patents

Fluorinated hydrocarbon-based mixed composition

Info

Publication number
JPH02215737A
JPH02215737A JP1033786A JP3378689A JPH02215737A JP H02215737 A JPH02215737 A JP H02215737A JP 1033786 A JP1033786 A JP 1033786A JP 3378689 A JP3378689 A JP 3378689A JP H02215737 A JPH02215737 A JP H02215737A
Authority
JP
Japan
Prior art keywords
composition
tert
fluorinated hydrocarbon
solvent
butyl 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
Application number
JP1033786A
Other languages
Japanese (ja)
Inventor
Akio Asano
浅野 昭雄
Toru Kamimura
徹 上村
Naohiro Watanabe
渡辺 直洋
Tateo Kitamura
健郎 北村
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 JP1033786A priority Critical patent/JPH02215737A/en
Publication of JPH02215737A publication Critical patent/JPH02215737A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To obtain a fluorinated hydrocarbon-based mixed composition, consisting of 1,1,2-trifluoroethane and tert-butyl chloride, usable as a substitute fluorocarbon for various applications, such as heating medium or foaming agent, and especially having excellent characteristics as a solvent. CONSTITUTION:The above-mentioned composition, obtained by blending (A) 60-95wt.%, preferably 80-90wt.% 1,1,2-trichlorotrifluoroethane with (B) 5-40wt.%, preferably 10-20wt.% tert-butyl chloride as essential components [the azeotropic composition is especially about 85wt.% component (A) and about 15wt.% component (B)], capable of reducing the amount thereof while satisfying excellent characteristics of conventional fluorocarbons and providing the same usage as that of the conventional single fluorocarbon due to the presence of the azeotropic composition and hardly any fluctuation of composition even in recycling. Since properties of dissolving and removing fluxes, oils, etc., are especially better than those of simple R113, the aforementioned incombustible or flame retardant composition is suitable as a detergent solvent substitute for the R113.

Description

【発明の詳細な説明】 [産業上の利用分野J 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混
合組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application J The present invention relates to a novel fluorinated hydrocarbon mixed composition that can be used as a fluorocarbon 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(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, non-flammable, and chemically stable, and various fluorocarbons with different standard boiling points are available, so they can be used to take advantage of these characteristics. Various types of fluorocarbons are used as solvents, blowing agents, propellants, refrigerants, etc. For example, 1,1,2-trichloro-1,2,2-trifluoroethane (R113) is used as a solvent, trichloromonofluoromethane (R11) is used as a blowing agent, and dichlorodifluoromethane (R12) is used as a propellant or refrigerant. It is used.

【発明の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] 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, which cause ozone. There is a movement to restrict the use of these conventional fluorocarbons because they are said to cause a chain reaction and destroy the ozone layer. 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1,1.2−トリクロロトリフルオロエタン(
R113)と塩化−tert−ブチルとからなるフッ素
化炭化水素系混合組成物に関するものである。本発明の
組成物は不燃又は難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単体よりも洗浄
力が高いため、R113の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 1,1,2-trichlorotrifluoroethane (
The present invention relates to a fluorinated hydrocarbon mixed composition comprising R113) and tert-butyl chloride. The composition of the present invention is nonflammable or flame retardant, has an azeotropic composition, and has higher detergency as a cleaning solvent than conventional R113 alone, 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ことから、本発明の
組成物としてはR113が60〜95重量%及び塩化−
tert−ブチルが5〜40重量%、好ましくはR11
3が80〜90重量%及び塩化−tert−ブチルが1
0〜20重量%であり、さらに好ましくはR113の約
85重量%と塩化−tert−ブチルの約15重量%か
らなる共沸組成物である。
Furthermore, the composition of the present invention has the advantage that there is little change in composition even when recycled, it can be used in the same way as conventional single fluorocarbons, and it does not require major changes in conventional technology. 60-95% by weight of R113 and chloride-
5 to 40% by weight of tert-butyl, preferably R11
3 is 80-90% by weight and tert-butyl chloride is 1
0 to 20% by weight, more preferably an azeotropic composition consisting of about 85% by weight of R113 and about 15% by weight of tert-butyl chloride.

本発明の組成物には、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、ペンタン、インペンタン、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
、i−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 composition of the present invention depending on the intended use. For example, when used as a solvent, hydrocarbons such as pentane, impentane, hexane, isohexane, heptane, and isohbutane,
Nitroalkanes such as nitromethane, nitroethane, nitropropane, diethylamine, triethylamine, isopropylamine, butylamine, isobutylamine,
Amines such as methanol, ethanol, n-propyl alcohol, i-propyl alcohol, n-butanol, alcohols such as i-butanol, ethers such as methyl cellosolve, tetrahydrofuran, 1,4-dioxane, acetone, methyl ethyl ketone , ketones such as methyl butyl ketone, and esters such as ethyl acetate, propyl acetate, butyl acetate, and the like can be added and mixed.

又、本発明の組成物を安定化する必要がある場合には、
安定化剤として、ニトロ化合物、フェノール類、アミン
類、エーテル類、アミシン類、エステル類、有機ホスフ
ァイト類、エポキサイド類、フラン類、アルコール類、
ケトン類およびトリアゾール類の群から選ばれる少なく
とも1種を添加することができる。添加重量としては、
特に限定されないが、混合組成物に対して1 ppm〜
10%、好ましくはloppm〜5%、さらに好ましく
はtoopp−〜3%である。
Additionally, if it is necessary to stabilize the composition of the present invention,
As stabilizers, nitro compounds, phenols, amines, ethers, amicins, esters, organic phosphites, epoxides, furans, alcohols,
At least one member selected from the group of ketones and triazoles can be added. As for the added weight,
Although not particularly limited, 1 ppm to mixed composition
10%, preferably loppm to 5%, more preferably toopp to 3%.

R113及び塩化−tert−ブチルからなる本発明の
混合組成物は、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、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かできる。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 mixed composition of the present invention consisting of R113 and tert-butyl chloride can be used for various purposes such as heat carriers and blowing agents, similar to conventional fluorocarbons, and especially when used as a solvent, it has a higher dissolving power than conventional R113. It is suitable because of its high value. Specific uses of solvents include flux, grease, oil,
Examples include removers for wax and ink, solvents for paints, extractants, cleaning agents and draining agents for glass, ceramics, plastics, rubber, various metal products, especially IC parts, electrical equipment, precision machinery, optical lenses, etc. I can do it. As the cleaning method, hand wiping, dipping, spraying, shaking, ultrasonic cleaning, steam cleaning, etc. may be employed.

[実施例] 実施例1 下記の組成から成る溶剤混合物1000 g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。
[Examples] 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g) RL13   (沸点47.6℃)600塩化−ter
t−ブチル(沸点50.7℃)400その結果46.5
℃に於て留分200g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 g) RL13 (Boiling point 47.6°C) 600 chloride-ter
t-Butyl (boiling point 50.7°C) 400 Result 46.5
200g of fraction was obtained at . As a result of measuring this product with a gas chromatograph, it had the following composition.

(組 成)      (重量%) R11385 塩化−tert−ブチル         15実施例
2 本発明の組成物(R113/塩化−tert−ブチル=
 85/ 15重量%)を用いて機械油の洗浄試験を行
なった。
(Composition) (% by weight) R11385 Tert-butyl chloride 15 Example 2 Composition of the present invention (R113/tert-butyl chloride=
85/15% by weight) was used to conduct a machine oil cleaning test.

5O3−304テストピース(25mmx 30mm+
X 2 mm厚)を機械油中に浸漬した後、本発明の前
記混合物に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。機械油の除去の度合いを
第1表に示す。
5O3-304 test piece (25mm x 30mm+
X 2 mm thick) was immersed in machine oil and then immersed in the mixture of the present invention for 5 minutes. A similar test was also conducted for R113 as a comparative example. Table 1 shows the degree of machine oil removal.

第  1  表 ない等の利点がある。又、溶剤としてよく使われている
R113単体よりもフラックスや油等の溶解除去性に優
れるためR113に替わる洗浄溶剤として好適である。
It has advantages such as not having Table 1. Furthermore, it is suitable as a cleaning solvent in place of R113 because it has better ability to dissolve and remove flux, oil, etc. than R113 alone, which is often used as a solvent.

0;良好に除去できる  ○;はぼ良好Δ;微量残存 
     ×;かなり残存[発明の効果]
0: Can be removed well ○: Good Δ: Trace amount remains
×; Significantly remaining [effect of invention]

Claims (1)

【特許請求の範囲】 1、1,1,2−トリクロロトリフルオロエタンと塩化
−tert−ブチルとからなるフッ素化炭化水素系混合
組成物。 2、1,1,2−トリクロロトリフルオロエタン60〜
95重量%と塩化−tert−ブチル5〜40重量%と
からなるフッ素化炭化水素系混合組成物。
[Claims] A fluorinated hydrocarbon mixed composition comprising 1,1,1,2-trichlorotrifluoroethane and tert-butyl chloride. 2,1,1,2-trichlorotrifluoroethane 60~
A fluorinated hydrocarbon mixed composition consisting of 95% by weight and 5 to 40% by weight of tert-butyl chloride.
JP1033786A 1989-02-15 1989-02-15 Fluorinated hydrocarbon-based mixed composition Pending JPH02215737A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1033786A JPH02215737A (en) 1989-02-15 1989-02-15 Fluorinated hydrocarbon-based mixed composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1033786A JPH02215737A (en) 1989-02-15 1989-02-15 Fluorinated hydrocarbon-based mixed composition

Publications (1)

Publication Number Publication Date
JPH02215737A true JPH02215737A (en) 1990-08-28

Family

ID=12396156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1033786A Pending JPH02215737A (en) 1989-02-15 1989-02-15 Fluorinated hydrocarbon-based mixed composition

Country Status (1)

Country Link
JP (1) JPH02215737A (en)

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