JPH0397794A - Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition - Google Patents

Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition

Info

Publication number
JPH0397794A
JPH0397794A JP23460789A JP23460789A JPH0397794A JP H0397794 A JPH0397794 A JP H0397794A JP 23460789 A JP23460789 A JP 23460789A JP 23460789 A JP23460789 A JP 23460789A JP H0397794 A JPH0397794 A JP H0397794A
Authority
JP
Japan
Prior art keywords
trichloroethane
composition
azeotropic
weight
amount
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
JP23460789A
Other languages
Japanese (ja)
Inventor
Toru Kamimura
徹 上村
Naohiro Watanabe
渡辺 直洋
Akio Asano
浅野 昭雄
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 JP23460789A priority Critical patent/JPH0397794A/en
Publication of JPH0397794A publication Critical patent/JPH0397794A/en
Pending legal-status Critical Current

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

PURPOSE:To provide the subject novel composition highly useful as a substitute for 1,1,1-trichloroethane and little in the fluctuation of the composition even when recycled, comprising sec - butyl chloride, etc., and 1,1,1-trichloroethane. CONSTITUTION:The objective composition comprises (A) sec - butyl chloride preferably in an amount of 30-55wt.% (especially 42.9wt.%) and 1,1,1- trichloroethane preferably in an amount of 45-70wt.% (especially 57.1wt.%), or comprises (B) isobutyl chloride preferably in an amount of 40-65wt.% (especially 49.4wt.%) and 1,1,1-trichloroethane, preferably in an amount of 35-60wt.% (especially 50.6wt.%).

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、溶剤等として優れた特性を有する新規な共沸
及び共沸用溶剤組戊物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a novel azeotrope and azeotropic solvent composition having excellent properties as a solvent and the like.

[従来の技術] 1, 1. 1− }リクロロエタンは適当な沸点およ
び溶解性を有し、比較的毒性が少ないことから、これら
の特性を活かして溶剤、揃釈剤等として広く使用されて
いる。
[Prior art] 1, 1. 1-} Lichloroethane has an appropriate boiling point and solubility, and is relatively less toxic, so it is widely used as a solvent, a diluent, etc. by taking advantage of these properties.

[発明が解決しようとする課題] 化学的に特に安定なフロンRll,R12, Rl 1
3等の完全ハロゲン化炭化水素は成層圏に達した際に太
陽光線により分解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事から、これら
特定フロンの生産量規制が実施されることとなった。ま
た、l, 1. 1− トリクロロエタンに関してもオ
ゾン層破壊の原因とされている塩素を有するため、環境
保護の観点より特定フロン同様に生産量規制の動きがあ
る。
[Problem to be solved by the invention] Chemically particularly stable fluorocarbons Rll, R12, Rl 1
When fully halogenated hydrocarbons such as Class 3 reach the stratosphere, they are decomposed by sunlight and generate chlorine radicals that cause a chain reaction with ozone and destroy the ozone layer. Therefore, the production volume of these specific fluorocarbons has been regulated. It happened. Also, l, 1. 1- Since trichloroethane also contains chlorine, which is considered to be a cause of ozone layer destruction, there are moves to regulate the production volume of trichloroethane in the same way as specified fluorocarbons from the perspective of environmental protection.

このため、従来より用いられてきた1, 1, ]一ト
リクロロエタンに代わり、オゾン層を破壊しにくい代替
物質の探索が活発に行なわれている。
Therefore, in place of the conventionally used 1, 1, ]-trichloroethane, there is active search for alternative substances that are less likely to deplete the ozone layer.

本発明は、従来の1.1.1−トリクロロエタンの使用
量を低減し、かつ該物質が有している優れた特性を満足
しながら代替物質として使用できる新規な1,1.1−
トリクロロエタン組成物を提供することを目的とするも
のである。
The present invention provides a novel 1,1.1-trichloroethane that can be used as a substitute while reducing the amount of conventional 1.1.1-trichloroethane used and satisfying the excellent properties of this substance.
The object is to provide a trichloroethane composition.

[評題を解決するための手段] 本発明は、塩化−SeC−ブチル、塩化イソブチルのい
ずれか一種およびl, 1. 1−トリクロロエタンと
からなる共沸および共沸様組成物に関するものである。
[Means for Solving the Problem] The present invention provides a method for solving the problem using one of -SeC-butyl chloride and isobutyl chloride; 1-Trichloroethane.

本発明の組成物は、共沸組成が存在する上、洗浄溶剤と
しては従来の1.1.1−1−リクロロエタンと同等の
洗浄力を有するため、被洗浄部材の劣化を起こす事なく
充分な洗浄が実施でき、かつ該規制物質である1, 1
. 1−トリクロロエタンの使用量を大幅に削減可能で
ある。また、非常に類似の物性を有するため現在用いて
いる洗浄機等の設備を大幅な仕様変更をすることなしに
多岐に渡った様々な洗浄方法での使用が可能である等の
長所を有しているため、i,i,x−トリクロロエタン
代替としてきわめて有用なものである。更に、リサイク
ルしても組成変動が少ないこと等多くの利点を有してい
る。
The composition of the present invention has an azeotropic composition and, as a cleaning solvent, has a cleaning power equivalent to that of conventional 1.1.1-1-lichloroethane, so it is sufficient without causing deterioration of the parts to be cleaned. 1, 1 which can be cleaned thoroughly and is a regulated substance.
.. The amount of 1-trichloroethane used can be significantly reduced. In addition, because they have very similar physical properties, they have the advantage of being able to be used in a wide variety of cleaning methods without making major changes to the specifications of equipment such as washing machines that are currently in use. Therefore, it is extremely useful as a substitute for i,i,x-trichloroethane. Furthermore, it has many advantages such as less compositional fluctuation even after recycling.

本発明における組成物の1, 1. 1−トリクロロエ
タンおよび塩化−see−ブチルの混合比は1,1.1
−トリクロロユタン45〜70重量%および塩化sec
ブチル30〜55重量%の共沸様組成が好ましく、更に
好ましくは1, 1,lトリクロロエタン57.1重量
%および塩化−SeC−ブチル42.9重量%である共
沸組成である。
Compositions 1, 1 of the present invention. The mixing ratio of 1-trichloroethane and -see-butyl chloride is 1,1.1
- 45-70% by weight of trichloroutane and sec chloride
An azeotrope-like composition of 30-55% by weight butyl is preferred, more preferably an azeotrope-like composition of 57.1% by weight 1,1,1 trichloroethane and 42.9% by weight -SeC-butyl chloride.

本発明における組成物の1.,1,1−トリクロロエタ
ンおよび塩化イソブチルの混合比は1, 1. 1−ト
リクロロエタン35〜60重量%および塩化イソブチル
40〜65重量%の共沸様組成が好ましく、更に好まし
くは1,1.1−トリクロロエタン50。6重量%およ
び塩化イソブチル49.4重量%である共沸組成である
1. Composition of the present invention. , 1,1-trichloroethane and isobutyl chloride at a mixing ratio of 1.1. An azeotrope-like composition of 35-60% by weight of 1-trichloroethane and 40-65% by weight of isobutyl chloride is preferred, more preferably an azeotrope-like composition of 50.6% by weight of 1,1.1-trichloroethane and 49.4% by weight of isobutyl chloride. It has a boiling composition.

本共沸組成物の共廊組成比は、混合する1.1.1−ト
リクロ口エタン等の純度や測定誤差等の影響により±1
、0重量%程度変動しつるものである。
The common composition ratio of this azeotropic composition is ±1 due to the influence of the purity of the 1.1.1-tricloethane to be mixed, measurement error, etc.
, it fluctuates by about 0% 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、ベンタン、インベンタン、ヘキサン、イソ
ヘキサン、ネオヘキサン、ヘブタン、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、ニトロブロバン等のニ
トロアルカン類、ジエチルアミン、トリエチルアミン、
イソブロビルアミン、プチルアミン、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−プロビル
アルコール,i−プロビルアルコール,n−ブチルアル
コール.i一ブチルアルコール,S−ブチルアルコール
,1−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、酢酸プロビル、
酢酸ブチル等のエステル類、ジクロロメタン、tran
s−1.2−ジクロロエチレン、cis−1. 2−ジ
クロロエチレ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、1
、1,2、2−テトラクロ口−1、2−ジフロロエタン
、1.1−ジクロロ−2.2,3,3.3−ペンタフロ
ロブロバン等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 composition of the present invention depending on the intended use. For example, in applications as a solvent, bentane, inventane, hexane, isohexane, neohexane, hebutane, isohexane,
.. Hydrocarbons such as 3-dimethylbutane and cyclopentane, nitroalkanes such as nitromethane, nitroethane and nitrobroban, diethylamine, triethylamine,
Amines such as isobrobylamine, butylamine, isobutylamine, methanol, ethanol, n-propyl alcohol, i-propyl alcohol, n-butyl alcohol. Alcohols such as monobutyl alcohol, S-butyl alcohol, 1-butyl alcohol, methyl cellosolve, tetrahydrofuran. 1. Ethers such as 4-dioxane, ketones such as acetone, methyl ethyl ketone, methyl butyl ketone, ethyl acetate, proyl acetate,
Esters such as butyl acetate, dichloromethane, tran
s-1.2-dichloroethylene, cis-1. Halogenated hydrocarbons such as 2-dichloroethylene, others, 1
, 1,2-trichloro-2,2-difluoroethane, 1
, 1,2,2-tetrachloro-1,2-difluoroethane, 1,1-dichloro-2,2,3,3,3-pentafluorobroban, and other fluorocarbons can be added as appropriate.

本発明の共沸および共沸様組成物は、従来の1. 1.
 1−トリクロロエタンと同様、各種用途に使用でき、
特に溶剤として用いた場合、従来の1. 1. 1−ト
リクロロエタンと同等の溶解力を有するため代替物質と
して好適である。
The azeotrope and azeotrope-like compositions of the present invention are similar to conventional 1. 1.
Like 1-trichloroethane, it can be used for various purposes,
Especially when used as a solvent, conventional 1. 1. It is suitable as a substitute substance because it has the same dissolving power as 1-trichloroethane.

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
各種部品、特にIC部品、電気機器、精密機械、光学レ
ンズ専の洗浄削や水切り剤等をあげることができる。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 uses of solvents include flux, grease,
Removal agents for oil, wax, ink, etc., paint solvents, extractants, glass, ceramics, plastics, rubber, various metal parts, especially IC parts, electrical equipment, precision machinery, optical lens cleaning and draining agents, etc. can be given. As a cleaning method, 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 第1表に示した各組成からなる混合物1000g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200gの留分を得た。こ
の時の留出温度および留分のガスクロマトグラフ測定結
果を第2表に示す。
Example 1 1000 g of a mixture consisting of each composition shown in Table 1 was placed in a distillation flask, and a rectification column with 20 theoretical plates was used.
Distillation was carried out under atmospheric pressure to obtain 200 g of each fraction. Table 2 shows the distillation temperature and gas chromatograph measurement results of the fraction at this time.

第l表 第2表 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・ SUS304製テストビース( 25mmX 30mm
X 2mm厚)を機械油(CQ−30,日本石油 製)
中に浸漬した後、本発明の前期組成物に5分間浸漬洗浄
した。比較例としてl, 1. 1〜トリクロロエタン
についても同様の試験を実施した。
Table 1 Table 2 Example 2 A machine oil cleaning test was conducted using the composition of the present invention. SUS304 test beads (25 mm x 30 mm)
x 2mm thick) with machine oil (CQ-30, manufactured by Nippon Oil)
After being immersed in the composition, the sample was washed by immersion in the composition of the present invention for 5 minutes. As a comparative example, 1. Similar tests were conducted for 1 to trichloroethane.

機械油の除去の度合を第3表に示す。Table 3 shows the degree of machine oil removal.

第3表 0;良好に除去できる、 ○;ほぼ良好△;微量残存、
     ×;かなり残量[発明の効果] 本発明の共沸および共沸様組成物は、従来の1. 1,
 l− トリクロロエタンが有している優れた特性を満
足しながら代替物質として使用できるとともに、リサイ
クルしても組成変動が小さいため、従来の1.1.1−
トリクロロエタン単一物と同等の使い方ができ、従来技
術の大幅な変更を要しない等の利点がある。また、溶剤
としてtti械油等の除去性能に優れるためi, i,
 i一トリクロロエタンに替わる脱脂洗浄溶剤として最
適である。
Table 3 0: Can be removed well, ○: Almost good △: A trace amount remains,
×: Significant residual amount [Effect of the invention] The azeotrope and azeotrope-like composition of the present invention have the same amount as the conventional 1. 1,
It can be used as a substitute material while satisfying the excellent properties of l-trichloroethane, and the composition change is small even when recycled, so it can be used as a substitute for conventional l-trichloroethane.
It has the advantage that it can be used in the same way as trichloroethane alone and does not require major changes in conventional technology. In addition, as a solvent, it has excellent removal performance of tti machine oil, etc., so i, i,
I-Ideal as a degreasing cleaning solvent in place of trichloroethane.

Claims (1)

【特許請求の範囲】 1,塩化−sec−ブチル、塩化イソブチルのいずれか
一種および1,1,1−トリクロロエタンとからなる共
沸および共沸様組成物。 2,1,1,1−トリクロロエタン45〜70重量%、
及び塩化−sec−ブチル30〜55重量%からなる請
求項1に記載の共沸様組成物。 3,1.1,1−トリクロロエタン57.1重量%、及
び塩化−sec−ブチル42.9重量%からなる請求項
1に記載の共沸組成物。 4,1,1,1−トリクロロエタン35〜60重量%、
及び塩化イソブチル45〜60重量%からなる請求項1
に記載の共沸様組成物。 5,1,1,1−トリクロロエタン50.6重量%、及
び塩化イソブチル49.4重量%からなる請求項1に記
載の共沸組成物。
[Scope of Claims] Azeotropic and azeotrope-like compositions comprising any one of 1, sec-butyl chloride and isobutyl chloride and 1,1,1-trichloroethane. 2,1,1,1-trichloroethane 45-70% by weight,
and 30 to 55% by weight of -sec-butyl chloride. The azeotropic composition according to claim 1, consisting of 57.1% by weight of 3,1.1,1-trichloroethane and 42.9% by weight of -sec-butyl chloride. 4,1,1,1-trichloroethane 35-60% by weight,
and 45 to 60% by weight of isobutyl chloride.
The azeotrope-like composition described in . The azeotropic composition according to claim 1, consisting of 50.6% by weight of 5,1,1,1-trichloroethane and 49.4% by weight of isobutyl chloride.
JP23460789A 1989-09-12 1989-09-12 Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition Pending JPH0397794A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23460789A JPH0397794A (en) 1989-09-12 1989-09-12 Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23460789A JPH0397794A (en) 1989-09-12 1989-09-12 Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition

Publications (1)

Publication Number Publication Date
JPH0397794A true JPH0397794A (en) 1991-04-23

Family

ID=16973688

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23460789A Pending JPH0397794A (en) 1989-09-12 1989-09-12 Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition

Country Status (1)

Country Link
JP (1) JPH0397794A (en)

Similar Documents

Publication Publication Date Title
JPH03176433A (en) Azeotropic and pseudoazeotropic composition containing trichlorodifluoroethane as principal component
JPH0397793A (en) Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main component
JPH0397794A (en) Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main composition
JPH0331224A (en) Fluorohydrocarbon azeotropic or pseudoazeotropic composition
JPH0397797A (en) Azeotropic and azeotropic-like compositions containing 1,1,1-trichloroethane as main component
JPH0374338A (en) Fluorinated hydrocarbon based azeotropic composition
JPH02207032A (en) Azeotropic mixture and azeotrope-like mixture of dichloropentafluoropropane
JPH0399029A (en) Fluorinated hydrocarbon based-azeotropic composition
JPH02311430A (en) Fluorohydrocarbon-based azeotropic composition
JPH0397795A (en) Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main component
JPH02273632A (en) Fluorinated hydrocarbon-based azeotropic mixture
JPH04359095A (en) Mixed solvent composition and azeotrope-like solvent composition
JPH0397796A (en) Azeotropic and azeotropic-like compositions containing 1,1,1-trichloroethane as main component
JPH0327331A (en) Fluorinated hydrocarbon based azeotropic and pseudo-azeotropic composition
JPH0399030A (en) Fluorinated hydrocarbon based-azeotropic composition
JPH02209835A (en) Azeotropic mixture and azeotrope-like mixture of 1-chloro-2,2,3,3-tetrafluoropropane
JPH0489439A (en) Dichloropentafluoropropane-based azeotropic composition and azeotropy-like composition
JPH03236334A (en) Azeotropic and azeotropic-like composition consisting mainly of trichlorodifluoroethane
JPH02212440A (en) Azeotropic and azeotrope-like composition of chlorotetrafluoropropane
JPH02209834A (en) Azeotropic mixture and pseudo-azeotropic mixture of 1-chloro-2,2,3,3-tetrafluoropropane
JPH0327330A (en) Fluorinated hydrocarbon based azeotropic and pseudo-azeotropic composition
JPH07278595A (en) Solvent composition
JPH02209831A (en) Azeotropic mixture and pseudo-azeotropic mixture of chlorotetrafluoropropane
JPH03173837A (en) Fluorinated hydrocarbon-based azeotropic composition
JPH02279634A (en) Fluorohydrocarbon-based azeotropic composition and pseudoazeotropic composition