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JPH05124990A - Azeotropy-like composition - Google Patents

Azeotropy-like composition

Info

Publication number
JPH05124990A
JPH05124990A JP3310207A JP31020791A JPH05124990A JP H05124990 A JPH05124990 A JP H05124990A JP 3310207 A JP3310207 A JP 3310207A JP 31020791 A JP31020791 A JP 31020791A JP H05124990 A JPH05124990 A JP H05124990A
Authority
JP
Japan
Prior art keywords
chlorobutane
composition
10mee
hfc
weight
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
JP3310207A
Other languages
Japanese (ja)
Inventor
Hideaki Kikuchi
秀明 菊地
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.)
Chemours Mitsui Fluoroproducts Co Ltd
Original Assignee
Du Pont Mitsui Fluorochemicals 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 Du Pont Mitsui Fluorochemicals Co Ltd filed Critical Du Pont Mitsui Fluorochemicals Co Ltd
Priority to JP3310207A priority Critical patent/JPH05124990A/en
Publication of JPH05124990A publication Critical patent/JPH05124990A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Manufacturing Of Printed Wiring (AREA)
  • Detergent Compositions (AREA)

Abstract

PURPOSE:To obtain the subject composition comprising a highly brominated hydrocarbon as a base, having azeotropic behavior or a behavior close to azeotropic behavior and excellent characteristics as a detergent by blending decafluoropentane with chlorobutane. CONSTITUTION:(A) 85-99wt.% 1,1,1,2,3,4,4,5,5,5-decafluoropentane is mixed with 15-1wt.% 1-chlorobutane, otherwise (B) 75-99wt.% 1,1,1,2,3,4,4,5,5,5- decafluoropentane is mixed with 25-1wt.% 2-chlorobutane, and optionally a stabilizersuch as a nitroalkane (preferably 0.05-0.5wt.%) to give the objective composition.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、高度に弗素化されたハ
イドロフルオロカーボンをベースとする共沸乃至それに
近い挙動を示す組成物に関するものである。更に詳しく
は、加工や錆止めとして金属部品に使用されているグリ
ースや加工油等の脱脂洗浄、半導体製造時のフラックス
除去の為に好適に使用されるほか、発泡剤、作動媒体、
電気絶縁剤等の用途を代替することが可能な共沸様組成
物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a highly fluorinated hydrofluorocarbon-based composition exhibiting azeotropic or similar behavior. More specifically, it is preferably used for degreasing and cleaning of grease and processing oil used for metal parts for processing and rust prevention, and flux removal during semiconductor manufacturing, as well as a foaming agent, working medium,
The present invention relates to an azeotropic composition capable of substituting for applications such as electrical insulating agents.

【0002】[0002]

【従来の技術】クロロフルオロカーボンは毒性が少なく
難燃性で、化学的、熱的に安定なものが多いため、溶
剤、発泡剤、冷媒等に広く使用され、フラックス除去等
の半導体製品の洗浄には、クロロフルオロカーボン系溶
剤である1,1,2-トリクロロ−1,2,2-トリフルオロエタン
(CFC-113,沸点約48℃)、或は塩素系溶剤である1,1,
1-トリクロロエタン等が使用されていた。
BACKGROUND OF THE INVENTION Chlorofluorocarbons are widely used as solvents, foaming agents, refrigerants, etc. for cleaning semiconductor products such as flux removal, because they are less toxic, flame-retardant and chemically and thermally stable. Is a chlorofluorocarbon-based solvent, 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113, boiling point about 48 ° C), or a chlorine-based solvent, 1,1,
1-Trichloroethane etc. were used.

【0003】[0003]

【発明が解決しようとする課題】しかしオゾン層保護の
観点から、ウイーン条約(1985年)やモントリオール議
定書(1987年)に基づき、わが国でもCFC-11(トリクロ
ロフルオロメタン)、CFC-12(ジクロロジフルオロメタ
ン)、 CFC-113、 CFC-114、CFC-115などのクロロフル
オロカーボンについては生産量削減、使用規制等が実施
された。また塩素系溶剤についても発ガン性が指摘され
ており、地下水汚染などの問題もあって使用規制が検討
されている。そこで本発明は、オゾン層を破壊する恐れ
が無く、発ガン性の問題がない、塩素を含まない新規な
ハイドロフルオロカーボンをベースとして、共沸乃至そ
れに近い挙動を示す組成物を提供することを目的とす
る。
[Problems to be Solved by the Invention] However, from the perspective of protecting the ozone layer, CFC-11 (trichlorofluoromethane) and CFC-12 (dichlorodifluoromethane) are also used in Japan based on the Vienna Convention (1985) and the Montreal Protocol (1987). For chlorofluorocarbons such as methane), CFC-113, CFC-114, CFC-115, etc., production volume reduction and usage restrictions were implemented. In addition, it has been pointed out that the chlorine-based solvent is also carcinogenic, and there are problems such as groundwater pollution, and its use is being regulated. Therefore, the present invention aims to provide a composition which does not have a risk of depleting the ozone layer, does not have a problem of carcinogenicity, and is azeotropic or has a behavior close to that based on a novel chlorine-free hydrofluorocarbon. And

【0004】[0004]

【課題を解決するための手段】本発明にかかわる共沸様
組成物は、デカフルオロペンタン及びクロロブタンから
なり、好ましくは85〜99重量%の1,1,1,2,3,4,4,5,5,5-
デカフルオロペンタン(以下HFC-43-10meeと記す)と15
〜1 重量%の1-クロロブタンからなるか、あるいは75〜
99重量%の1,1,1,2,3,4,4,5,5,5-デカフルオロペンタン
と25〜1 重量%の2-クロロブタンからなることを特徴と
する。
The azeotrope-like composition according to the present invention comprises decafluoropentane and chlorobutane, preferably 85-99% by weight of 1,1,1,2,3,4,4, 5,5,5-
Decafluoropentane (hereinafter referred to as HFC-43-10mee) and 15
~ 1% by weight 1-chlorobutane, or 75 ~
It is characterized by comprising 99% by weight of 1,1,1,2,3,4,4,5,5,5-decafluoropentane and 25 to 1% by weight of 2-chlorobutane.

【0005】実施例で用いたHFC-43-10meeは沸点が5
4.7℃であった。1-クロロブタン又は2-クロロブタン
は市販の溶剤グレードのものを使用できる。
HFC-43-10mee used in the examples has a boiling point of 5
It was 4.7 ° C. Commercially available solvent-grade 1-chlorobutane or 2-chlorobutane can be used.

【0006】本発明の組成物は共沸乃至それに近い挙動
を示す組成であるため、使用工程において蒸留操作があ
っても成分変化が少ないので該組成物の特性を維持する
ことができ、また組成物の回収や再利用に好都合であ
り、かつ炭化水素の溶解性がデカフルオロペンタンのみ
の場合よりも向上する。
Since the composition of the present invention is a composition which exhibits azeotropic behavior or a behavior close to it, the characteristics of the composition can be maintained because the composition does not change much even if a distillation operation is carried out in the use process. It is convenient for the recovery and reuse of substances, and the solubility of hydrocarbons is improved as compared with the case of decafluoropentane alone.

【0007】本発明の共沸様組成物中には、必要によっ
て安定化剤として従来クロロフルオロカーボンに用いら
れてきたニトロアルカン類、エポキシド類、フラン類、
ベンゾトリアゾール類、フェノール類、アミン類、ホス
フェイト類から選ばれる少なくとも1種が含まれていて
も構わない。安定剤の配合量は、共沸様組成物に対して
0.01〜5重量%、好ましくは0.05〜0.5重量
%である。
In the azeotrope-like composition of the present invention, nitroalkanes, epoxides, furans, which have been conventionally used as stabilizers for chlorofluorocarbons, if necessary,
At least one selected from benzotriazoles, phenols, amines, and phosphates may be contained. The amount of the stabilizer compounded is 0.01 to 5% by weight, preferably 0.05 to 0.5% by weight, based on the azeotropic composition.

【0008】洗浄剤用途として具体的には、フラック
ス、油脂、バフ研磨剤などの汚染物除去のため、金属部
品、プラスチック部品、ゴム製品や、これらを組み合わ
せた精密機械部品、電子部品の洗浄剤や、ドライクリー
ニング用洗浄剤として用いられる。洗浄剤として用いる
場合、常温洗浄法でのぬぐい落とし、浸漬、はけ洗い、
フラッシュ、スプレー、超音波洗浄や、加熱洗浄法での
沸騰状態での浸漬、蒸気ゆすぎ、蒸気洗浄等が適用で
き、これらを組み合わせるとより効果的である。
Specifically, as a cleaning agent application, a cleaning agent for metal parts, plastic parts, rubber products, precision machine parts and electronic parts combining these for removing contaminants such as flux, oil and buffing agent. Also used as a cleaning agent for dry cleaning. When used as a cleaning agent, wipe with normal temperature cleaning method, dip, brush wash,
Flashing, spraying, ultrasonic cleaning, immersion in a boiling state by a heating cleaning method, steam rinsing, steam cleaning, etc. can be applied, and it is more effective to combine them.

【0009】本発明の共沸様組成物は従来のフロンと同
様に、洗浄剤の他、発泡剤、作動媒体、フルオロポリマ
ー重合用溶剤、電気絶縁剤等の各種用途にも使用でき
る。
The azeotrope-like composition of the present invention can be used for various purposes such as a foaming agent, a working medium, a solvent for fluoropolymer polymerization, an electric insulating agent, etc., as well as a conventional CFC.

【0010】以下実施例により本発明を詳細に説明す
る。
The present invention will be described in detail below with reference to examples.

【0011】[0011]

【実施例1】還流器を備えたフラスコ(300ml)
に、あらかじめ1-クロロブタン(和光純薬製)濃度を調
節したHFC-43-10meeと1-クロロブタンとの混合液を約7
0g入れ、ヒーターで沸騰させた。約20分後に温度が
一定になったところでフラスコ内の液相及び気相の組成
をガスクロマトグラフィー(島津製作所製:GC-14A)に
より分析し、またその時の気相温度を測定した。1-クロ
ロブタン濃度を変えて上記の試験を繰り返した。試験結
果を表1に示す。また表1の結果より得たHFC-43-10mee
とクロロブタンとの混合組成物の気液平衡曲線を図1に
示す。
Example 1 Flask equipped with a reflux condenser (300 ml)
In addition, a mixture of HFC-43-10mee and 1-chlorobutane, the concentration of 1-chlorobutane (manufactured by Wako Pure Chemical Industries) was previously adjusted to about 7
0 g was put and it was boiled with a heater. After about 20 minutes, when the temperature became constant, the composition of the liquid phase and the gas phase in the flask was analyzed by gas chromatography (Shimadzu Corporation: GC-14A), and the gas phase temperature at that time was measured. The above test was repeated with different concentrations of 1-chlorobutane. The test results are shown in Table 1. HFC-43-10mee obtained from the results in Table 1
The vapor-liquid equilibrium curve of the mixed composition of chlorobutane and chlorobutane is shown in FIG.

【表1】 [Table 1]

【0012】表1及び図1から明らかなように、HFC-43
-10meeと1-クロロブタンの混合液はHFC-43-10meeが75〜
99重量%、1-クロロブタンが25〜1 重量%の範囲、特に
HFC-43-10meeが85〜99重量%、1-クロロブタンが15〜1
重量%の範囲では沸点がほぼ一定で、気相と液相の組成
がほぼ同一となり、共沸様組成物となっている。HFC-43
-10meeが75重量%より少なく1-クロロブタンが25重量%
より多くなると気液相の組成の差が大きくなる。
As is clear from Table 1 and FIG. 1, HFC-43
The mixture of -10mee and 1-chlorobutane has HFC-43-10mee of 75-
99% by weight, 25-1% by weight of 1-chlorobutane, especially
85-99% by weight of HFC-43-10mee, 15-1 of 1-chlorobutane
In the range of wt%, the boiling point is almost constant, the compositions of the gas phase and the liquid phase are almost the same, and the composition is an azeotropic composition. HFC-43
-10mee less than 75% by weight 1-chlorobutane 25% by weight
The larger the amount, the larger the difference in the composition of the gas-liquid phase.

【0013】[0013]

【実施例2】還流器を備えたフラスコ(300ml)
に、あらかじめ2-クロロブタン(和光純薬製)濃度を調
節したHFC-43-10meeと2-クロロブタンとの混合液を約7
0g入れ、ヒーターで沸騰させた。約20分後に温度が
一定になったところでフラスコ内の液相及び気相の組成
をガスクロマトグラフィー(島津製作所製:GC-14A)に
より分析し、またその時の気相温度を測定した。1-クロ
ロブタン濃度を変えて上記の試験を繰り返した。試験結
果を表2に示す。また表2の結果より得たHFC-43-10mee
とクロロブタンとの混合組成物の気液平衡曲線を図2に
示す。
Example 2 Flask equipped with a reflux condenser (300 ml)
In addition, about 7 parts of a mixed solution of HFC-43-10mee and 2-chlorobutane, in which the concentration of 2-chlorobutane (manufactured by Wako Pure Chemical Industries) was adjusted in advance.
0 g was put and it was boiled with a heater. After about 20 minutes, when the temperature became constant, the composition of the liquid phase and the gas phase in the flask was analyzed by gas chromatography (Shimadzu Corporation: GC-14A), and the gas phase temperature at that time was measured. The above test was repeated with different concentrations of 1-chlorobutane. The test results are shown in Table 2. HFC-43-10mee obtained from the results in Table 2
The vapor-liquid equilibrium curve of the mixed composition of chlorobutane and chlorobutane is shown in FIG.

【表2】 [Table 2]

【0014】表2及び図2から明らかなように、HFC-43
-10meeと2-クロロブタンの混合液はHFC-43-10meeが75〜
99重量%、2-クロロブタンが25〜1 重量%の範囲、特に
HFC-43-10meeが80〜99重量%、2-クロロブタンが20〜1
重量%の範囲では沸点がほぼ一定で、気相と液相の組成
がほぼ同一となり、明らかに共沸様組成物となってい
る。HFC-43-10meeが75重量%より少なく2-クロロブタン
が25重量%より多くなると気液相の組成の差が大きくな
る。
As is clear from Table 2 and FIG. 2, HFC-43
HFC-43-10mee is 75 ~ for mixed liquid of -10mee and 2-chlorobutane
99% by weight, in the range of 25 to 1% by weight of 2-chlorobutane, especially
HFC-43-10mee 80-99% by weight, 2-chlorobutane 20-1
In the range of wt%, the boiling point is almost constant, and the compositions of the gas phase and the liquid phase are almost the same, and the composition is obviously an azeotrope-like composition. When HFC-43-10mee is less than 75% by weight and 2-chlorobutane is more than 25% by weight, the difference in composition of gas-liquid phase becomes large.

【0015】[0015]

【実施例3】サンプル瓶(20ml)に、HFC-43-10mee
9.5g及び1-クロロブタン0.5gを採り室温で混合
し、その中に冷凍機油(アトモスHAB15F:日本石油製)
0.1gを入れ室温で手で振って撹拌した。冷凍機油は
該混合組成物に均一に溶解した。
[Example 3] HFC-43-10mee was added to a sample bottle (20 ml).
9.5 g and 1-chlorobutane 0.5 g are taken and mixed at room temperature, and a refrigerating machine oil (Atmos HAB15F: made by Nippon Oil Co., Ltd.)
0.1 g was added, and the mixture was shaken by hand at room temperature and stirred. Refrigerating machine oil was uniformly dissolved in the mixed composition.

【0016】[0016]

【実施例4】サンプル瓶(20ml)に、HFC-43-10mee
8.5g及び2-クロロブタン1.5gを採り室温で混合
し、その中に冷凍機油(アトモスHAB15F:日本石油製)
0.1gを入れ室温で手で振って撹拌した。冷凍機油は
該混合組成物に均一に溶解した。
[Example 4] HFC-43-10mee was added to a sample bottle (20 ml).
8.5 g and 1.5 g of 2-chlorobutane are taken and mixed at room temperature, and the refrigerating machine oil (Atmos HAB15F: made by Nippon Oil Co., Ltd.)
0.1 g was added, and the mixture was shaken by hand at room temperature and stirred. Refrigerating machine oil was uniformly dissolved in the mixed composition.

【0017】[0017]

【比較例1】サンプル瓶(20ml)に、HFC-43-10mee
を10gを計り取り、その中に冷凍機油(アトモスHAB1
5F:日本石油製)0.1gを入れ室温で手で振って撹拌
したところ、静置後二層分離した。
[Comparative Example 1] HFC-43-10mee was added to a sample bottle (20 ml).
Weigh 10 g of the oil and put it in the refrigerator oil (Atmos HAB1
5F: manufactured by Nippon Oil Co., Ltd.) (0.1 g) was added, and the mixture was shaken by hand at room temperature and stirred, and after standing, two layers were separated.

【0018】[0018]

【発明の効果】本発明の組成物は、実施例より明かなよ
うにCFC-113 (沸点約48℃)と沸点が近く、従来用い
てきた装置をそのまま使用でき、また共沸乃至はそれに
近い挙動を示すので、液管理が容易である。また油脂に
対する溶解性がHFC-43-10mee単独の場合よりも大きいた
め、加工や錆止めとして金属部品に使用されるグリース
や加工油等の脱脂洗浄そして半導体製造時のフラックス
除去等に有用である。
EFFECTS OF THE INVENTION The composition of the present invention has a boiling point close to that of CFC-113 (boiling point of about 48 ° C.) as is clear from the examples, and the conventional equipment can be used as it is, and azeotropic or close to it. Since it behaves, liquid management is easy. Further, since it has a higher solubility in oils and fats than HFC-43-10mee alone, it is useful for degreasing and cleaning grease and processing oils used for metal parts for processing and rust prevention, and flux removal during semiconductor manufacturing.

【図面の簡単な説明】[Brief description of drawings]

【図1】HFC-43-10meeと1-クロロブタンとの混合洗浄剤
組成物の気液平衡曲線を示す図である。
FIG. 1 is a view showing a gas-liquid equilibrium curve of a mixed detergent composition of HFC-43-10mee and 1-chlorobutane.

【図2】HFC-43-10meeと2-クロロブタンとの混合洗浄剤
組成物の気液平衡曲線を示す図である。
FIG. 2 is a view showing a gas-liquid equilibrium curve of a mixed detergent composition of HFC-43-10mee and 2-chlorobutane.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C23G 5/028 7308−4K // H05K 3/26 6736−4E ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location C23G 5/028 7308-4K // H05K 3/26 6736-4E

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 デカフルオロペンタン及びクロロブタン
からなることを特徴とする共沸様組成物。
1. An azeotropic composition comprising decafluoropentane and chlorobutane.
【請求項2】 85〜99重量%の1,1,1,2,3,4,4,5,5,5-デ
カフルオロペンタンと15〜1 重量%の1-クロロブタンか
らなる請求項1記載の共沸様組成物。
2. The composition according to claim 1, which comprises 85 to 99% by weight of 1,1,1,2,3,4,4,5,5,5-decafluoropentane and 15 to 1% by weight of 1-chlorobutane. An azeotropic composition.
【請求項3】 75〜99重量%の1,1,1,2,3,4,4,5,5,5-デ
カフルオロペンタンと25〜1 重量%の2-クロロブタンか
らなる請求項1記載の共沸様組成物。
3. The composition according to claim 1, which comprises 75 to 99% by weight of 1,1,1,2,3,4,4,5,5,5-decafluoropentane and 25 to 1% by weight of 2-chlorobutane. An azeotropic composition.
JP3310207A 1991-10-30 1991-10-30 Azeotropy-like composition Pending JPH05124990A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3310207A JPH05124990A (en) 1991-10-30 1991-10-30 Azeotropy-like composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3310207A JPH05124990A (en) 1991-10-30 1991-10-30 Azeotropy-like composition

Publications (1)

Publication Number Publication Date
JPH05124990A true JPH05124990A (en) 1993-05-21

Family

ID=18002483

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3310207A Pending JPH05124990A (en) 1991-10-30 1991-10-30 Azeotropy-like composition

Country Status (1)

Country Link
JP (1) JPH05124990A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5578137A (en) * 1993-08-31 1996-11-26 E. I. Du Pont De Nemours And Company Azeotropic or azeotrope-like compositions including 1,1,1,2,3,4,4,5,5,5-decafluoropentane
WO1999035210A1 (en) * 1998-01-02 1999-07-15 E.I. Du Pont De Nemours And Company Decafluoropentane compositions
EP0994929A4 (en) * 1997-07-09 2001-02-21 Great Lakes Chemical Corp Azeotrope and azeotrope-like compositions of 1-bromopropane and highly fluorinated hydrocarbons
USRE39819E1 (en) 1998-07-24 2007-09-04 Atofina Cleaning or drying compositions based on 1,1,1,2,3,4,4,5,5,5-decafluoropentane
KR20180044638A (en) * 2016-10-24 2018-05-03 동우 화인켐 주식회사 Composition for removing acrylic resin

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5578137A (en) * 1993-08-31 1996-11-26 E. I. Du Pont De Nemours And Company Azeotropic or azeotrope-like compositions including 1,1,1,2,3,4,4,5,5,5-decafluoropentane
EP0994929A4 (en) * 1997-07-09 2001-02-21 Great Lakes Chemical Corp Azeotrope and azeotrope-like compositions of 1-bromopropane and highly fluorinated hydrocarbons
WO1999035210A1 (en) * 1998-01-02 1999-07-15 E.I. Du Pont De Nemours And Company Decafluoropentane compositions
USRE39819E1 (en) 1998-07-24 2007-09-04 Atofina Cleaning or drying compositions based on 1,1,1,2,3,4,4,5,5,5-decafluoropentane
KR20180044638A (en) * 2016-10-24 2018-05-03 동우 화인켐 주식회사 Composition for removing acrylic resin

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