JPH02206698A - Fluorinated hydrocarbon mixed solvent composition - Google Patents

Fluorinated hydrocarbon mixed solvent composition

Info

Publication number
JPH02206698A
JPH02206698A JP2393689A JP2393689A JPH02206698A JP H02206698 A JPH02206698 A JP H02206698A JP 2393689 A JP2393689 A JP 2393689A JP 2393689 A JP2393689 A JP 2393689A JP H02206698 A JPH02206698 A JP H02206698A
Authority
JP
Japan
Prior art keywords
fluorinated hydrocarbon
mixed solvent
solvent composition
fluorocarbons
hydrocarbon mixed
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
JP2393689A
Other languages
Japanese (ja)
Inventor
Akio Asano
浅野 昭雄
Naohiro Watanabe
渡辺 直洋
Shunichi Samejima
鮫島 俊一
Tateo Kitamura
健郎 北村
Toru Kamimura
徹 上村
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 JP2393689A priority Critical patent/JPH02206698A/en
Publication of JPH02206698A publication Critical patent/JPH02206698A/en
Pending legal-status Critical Current

Links

Landscapes

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

Abstract

PURPOSE:To obtain the title novel composition which is especially effective for cleaning fat and oil as a substitute of CFC without destruction of the ozone layer and any adverse effect on metals and plastics by using a specific fluorinated hydrocarbon and flons. CONSTITUTION:The subject composition is composed of (A) at least one fluorinated hydrocarbon selected from the group consisting of CClF2CF2CHCl2, CCl2FCF2CHClF, CF3CF2CHCl2, CClF2CF2CHClF, CClF2CF2CH2Cl, CHF2CF2 CHClF, CH3CF2CCl2F, CHF2CF2CH2Cl, CH2ClCF2CH2Cl, CHCl2CF2CH3, CH3CF2 CH2Cl, CClF2CF2CH2F, CH2ClCF2CHClF, CH2FCF2CHCl2, CH2FCF2CHCIF, CClF2CF2CH3, CH2FCF2CH2Cl, and CH3CF2CHClF and (B) a CFC other than components A.

Description

【発明の詳細な説明】 [産業上の利用分野]。[Detailed description of the invention] [Industrial application field].

本発明は、代替フロンとして使用できると共に、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混合
溶剤組成物に関するものである。
The present invention relates to a novel fluorinated hydrocarbon mixed solvent composition that can be used as a CFC substitute and has excellent properties as a solvent.

[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
特性を生かして精密機器類の脱脂、プリント基板のワッ
クス除去等のための洗浄剤として1,1.2− トリク
ロロ−1,2,2−トリプルオロエタン(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, non-flammable, and chemically stable, and various types of fluorocarbons with different standard boiling points are available.Using these characteristics, this product can be used as a cleaning agent for degreasing precision equipment, removing wax from printed circuit boards, etc. , 1.2-trichloro-1,2,2-triple oroethane (R113) and trichloromonofluoromethane (R11) as blowing agent.
), dichlorodifluoromethane (R12) is used as a propellant and 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ことから、これら
の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策が活発に行われている。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混合物を提供することを目的とする
ものである。
[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, which are converted into ozone. There is a movement to restrict the use of these conventional fluorocarbons because they cause a chain reaction and destroy the ozone layer. For this reason, active efforts are being made to find alternative fluorocarbons that are less likely to deplete the ozone layer in place of these conventional fluorocarbons. An object of the present invention is to provide a new fluorocarbon mixture 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 CHF2CF2CH2Cl (R224ca)、CC1
2FCF2CHCIF (R224cb)、CHFCF
2CCl 2 (R225c a )、CHF2CF2
CH2Cl (R225cb)、CClF2CF2CH
2Cl (R234cc)、CHF2CF2CHCI 
F (R235c a )、CH3CF2CCl2F 
(R243cc)、CHF2CF2CH2Cl (R2
440a)、CH2ClCF2CH2Cl  (R25
2ca)。
[Means for solving the problem] The present invention provides CHF2CF2CH2Cl (R224ca), CC1
2FCF2CHCIF (R224cb), CHFCF
2CCl2 (R225ca), CHF2CF2
CH2Cl (R225cb), CClF2CF2CH
2Cl (R234cc), CHF2CF2CHCI
F (R235c a ), CH3CF2CCl2F
(R243cc), CHF2CF2CH2Cl (R2
440a), CH2ClCF2CH2Cl (R25
2ca).

CHC12CF2CH3(R252c b)、CH3C
F2CH2Cl  (R262c a)、CHF2CF
2CC12F  (R225c c)、CHCI FC
F2CHCI F (R234c a)、CHF2CF
2CHC12(R234c b)、CHF2F2CC1
2F  (R234c d)、CF3CF2CH2Cl
  (R235cb)、CG I F2CF2CH2F
  (R235c c)、CH2Cl CF2CHCl
 F (R243c a)、CH2FCF2CHC12
(R243c b)、CH2FCF2CHCI F  
(R244a b)、CG I F2CF2CH3(R
244c c)、CH2FCF2CH2Cl  (R2
53c a)、及びCH2OF2CHCI F (R2
53c b )の群から選ばれる少なくとも1種と上記
以外のフロンであって沸点が20℃〜100’Cの範囲
から選ばれる1種以上のものからなる弗素化炭化水素系
混合溶剤組成物に関するものである。
CHC12CF2CH3 (R252c b), CH3C
F2CH2Cl (R262c a), CHF2CF
2CC12F (R225c c), CHCI FC
F2CHCI F (R234c a), CHF2CF
2CHC12 (R234c b), CHF2F2CC1
2F (R234c d), CF3CF2CH2Cl
(R235cb), CG I F2CF2CH2F
(R235c c), CH2Cl CF2CHCl
F (R243c a), CH2FCF2CHC12
(R243c b), CH2FCF2CHCI F
(R244a b), CG I F2CF2CH3 (R
244c c), CH2FCF2CH2Cl (R2
53c a), and CH2OF2CHCI F (R2
Regarding a fluorinated hydrocarbon mixed solvent composition comprising at least one member selected from the group of 53c b) and one or more fluorocarbons other than the above with a boiling point in the range of 20°C to 100’C. It is.

本発明の組成物は不燃性又は難燃性であり、且つ従来の
フロン類と同等以上の洗浄力を有するものである。
The composition of the present invention is nonflammable or flame retardant, and has cleaning power equivalent to or higher than that of conventional fluorocarbons.

本発明に用いられる沸点が20〜100℃のフロンとし
て好ましいものは、 R11,R112、R112a、R113、R113a
、R122、R122a、R122b、R123,R1
23a、R123b、R131a、R132、R132
a、R132b、R132c。
Preferable fluorocarbons with a boiling point of 20 to 100°C used in the present invention are R11, R112, R112a, R113, and R113a.
, R122, R122a, R122b, R123, R1
23a, R123b, R131a, R132, R132
a, R132b, R132c.

R141、R141b、R142、R151゜R152
、R1112(cis)、R1112(trans)、
R1121及びR1121aであり、これらの群から少
なくとも1種以上が組み合わせて用いられる。
R141, R141b, R142, R151°R152
, R1112 (cis), R1112 (trans),
R1121 and R1121a, and at least one kind from these groups is used in combination.

本発明のR224ea、R224,cb、R225ca
、R225cb、R234cc、R235ca、R24
3cc、R244ca、R252ca、R252eb、
R262ca。
R224ea, R224, cb, R225ca of the present invention
, R225cb, R234cc, R235ca, R24
3cc, R244ca, R252ca, R252eb,
R262ca.

R225cc、R234ca、R234cb、R234
cd、R235cb、R235cc、R243ca、R
243cb、R244eb。
R225cc, R234ca, R234cb, R234
cd, R235cb, R235cc, R243ca, R
243cb, R244eb.

R244cc、  R253ca、  R253cb、
の各々の、上記以外のフロンで沸点が20〜100℃の
Wi囲のものとの混合物中の混合割合は20〜95重量
%、好ましくは40〜90重量%、さらに好ましくは5
0〜80重量%である。
R244cc, R253ca, R253cb,
The mixing ratio of each of these with CFCs other than those mentioned above with a boiling point of 20 to 100 ° C. in the range Wi is 20 to 95% by weight, preferably 40 to 90% by weight, more preferably 5% by weight.
It is 0 to 80% by weight.

本発明の混合溶剤組成物に共沸組成が存在する場合には
その共沸組成での使用が好ましい。
When the mixed solvent composition of the present invention has an azeotropic composition, it is preferably used in that azeotropic composition.

本発明の弗素化炭化水素系混合溶剤組成物は、従来の各
種用途に使用出来、特に従来の単独溶剤よりも洗浄力が
優れている点で有利である。
The fluorinated hydrocarbon mixed solvent composition of the present invention can be used in various conventional applications, and is particularly advantageous in that it has better cleaning power than conventional single solvents.

本発明の混合溶剤組成物の具体的な用途としては油、ワ
ックス、グリース等の除去剤、塗料用溶剤、シミ抜き剤
、ドライクリーニング用溶剤として、特に精密機器、プ
リント基板、光学レンズ等の洗浄剤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 超音
波洗浄、蒸気洗浄等を採用すればよい。
The mixed solvent composition of the present invention is specifically used as a remover for oil, wax, grease, etc., as a paint solvent, as a stain remover, and as a dry cleaning solvent, especially for cleaning precision instruments, printed circuit boards, optical lenses, etc. Agents can be mentioned. As cleaning methods, hand wiping, dipping, spray ultrasonic cleaning, steam cleaning, etc. may be used.

[実施例コ 第1表〜第5表に示す本発明の混合溶剤組成物を用いて
機械油の洗浄試験を行った。
[Example 2] Machine oil cleaning tests were conducted using the mixed solvent compositions of the present invention shown in Tables 1 to 5.

5US−304のテストピース(25mmX30mrn
X2mm厚)を機械油(CQ−30、日本石油製)に浸
漬した後、本発明の混合溶剤組成物中に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っ
た。機械油の除去の度合を第1表〜第5表に示す。
5US-304 test piece (25mmX30mrn
x 2 mm thick) was immersed in machine oil (CQ-30, manufactured by Nippon Oil) and then immersed in the mixed solvent composition of the present invention for 5 minutes. As a comparative example, a similar test was conducted on R113. Tables 1 to 5 show the degree of machine oil removal.

第 表 内は混合比 [重量%コ 内は混合比 [重量%コ 内は混合比 [重量%] 第 表 ()内は混合比[重量%] ◎;良好に除去できる。 ○;はぼ良好。No. table The inside is the mixing ratio [Weight% The inside is the mixing ratio [Weight% The inside is the mixing ratio [weight%] No. table (): Mixing ratio [wt%] ◎; Can be removed well. ○: Good condition.

△;微量残存。     Xフかなり残存。△; Trace amount remaining. There is quite a bit of X remaining.

内は混合比 [重量%コ [発明の効果コ 本発明の弗素化炭化水素系混合溶剤組成物は実施例から
明らかなように、例えば油脂類の洗浄効果等に優れたも
のである。又、従来使用されていたR113と同様に適
度な溶解力を持つことから、金属、プラスチック等から
なる複合部品に悪影響を与えることなく洗浄することが
できる。
The figures indicate the mixing ratio [wt%] [Effects of the Invention] As is clear from the Examples, the fluorinated hydrocarbon mixed solvent composition of the present invention is excellent in cleaning effects, for example, on oils and fats. Also, like the conventionally used R113, it has a suitable dissolving power, so it can clean composite parts made of metal, plastic, etc. without adversely affecting them.

Claims (1)

【特許請求の範囲】 1、CClF_2CF_2CHCl_2、 CCl_2FCF_2CHClF、 CF_3CF_2CHCl_2、CClF_2CF_2
CHClF、CClF_2CF_2CH_2Cl、 CHF_2CF_2CHClF、CH_3CF_2CC
l_2F、CHF_2CF_2CH_2Cl、 CH_2ClCF_2CH_2Cl、CHCl_2CF
_2CH_3、CH_3CF_2CH_2Cl、CHF
_2CF_2CCl_2F、CHClFCF_2CHC
lF、 CHF_2CF_2CHCl_2、CH_2FCF_2
CCl_2F、CF_3CF_2CH_2Cl、CCl
F_2CF_2CH_2F、CH_2ClCF_2CH
ClF、 CH_2FCF_2CHCl_2、CH_2FCF_2
CHClF、CClF_2CF_2CH_3、CH_2
FCF_2CH_2Cl、CH_3CF_2CHClF
の群から選ばれる1種以上と上記以外のフロン類とから
なる弗素化炭化水素系混合溶剤組成物。
[Claims] 1. CClF_2CF_2CHCl_2, CCl_2FCF_2CHClF, CF_3CF_2CHCl_2, CClF_2CF_2
CHClF, CClF_2CF_2CH_2Cl, CHF_2CF_2CHClF, CH_3CF_2CC
l_2F, CHF_2CF_2CH_2Cl, CH_2ClCF_2CH_2Cl, CHCl_2CF
_2CH_3, CH_3CF_2CH_2Cl, CHF
_2CF_2CCl_2F, CHClFCF_2CHC
IF, CHF_2CF_2CHCl_2, CH_2FCF_2
CCl_2F, CF_3CF_2CH_2Cl, CCl
F_2CF_2CH_2F, CH_2ClCF_2CH
ClF, CH_2FCF_2CHCl_2, CH_2FCF_2
CHClF, CClF_2CF_2CH_3, CH_2
FCF_2CH_2Cl, CH_3CF_2CHClF
A fluorinated hydrocarbon mixed solvent composition comprising one or more selected from the group of fluorocarbons and fluorocarbons other than those mentioned above.
JP2393689A 1989-02-03 1989-02-03 Fluorinated hydrocarbon mixed solvent composition Pending JPH02206698A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2393689A JPH02206698A (en) 1989-02-03 1989-02-03 Fluorinated hydrocarbon mixed solvent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2393689A JPH02206698A (en) 1989-02-03 1989-02-03 Fluorinated hydrocarbon mixed solvent composition

Publications (1)

Publication Number Publication Date
JPH02206698A true JPH02206698A (en) 1990-08-16

Family

ID=12124415

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2393689A Pending JPH02206698A (en) 1989-02-03 1989-02-03 Fluorinated hydrocarbon mixed solvent composition

Country Status (1)

Country Link
JP (1) JPH02206698A (en)

Similar Documents

Publication Publication Date Title
JPH01141995A (en) Fluorinated hydrocarbon-based azeotropic mixture
JPH01103686A (en) Fluorinated hydrocarbon mixture
JP2734624B2 (en) Fluorinated hydrocarbon-based azeotropic compositions
JPH0327328A (en) Fluorinated hydrocarbon-based solvent composition
JPH0397793A (en) Azeotropic and azeotropic-like composition containing 1,1,1-trichloroethane as main component
JPH02206698A (en) Fluorinated hydrocarbon mixed solvent composition
JP2734623B2 (en) Fluorinated hydrocarbon-based azeotropic compositions
JPH0317034A (en) Fluorinated hydrocarbon-based solvent composition
JPH06346095A (en) Fluorine based cleansing solvent composition
JPH0317032A (en) Fluorinated hydrocarbon-based solvent composition
JP2737249B2 (en) Fluorinated hydrocarbon pseudoazeotrope
JPH0327329A (en) Fluorinated hydrocarbon-based solvent composition
JPH02204466A (en) Fluorinated hydrocarbon mixed solvent composition
JPH0317033A (en) Fluorinated hydrocarbon-based solvent composition
JPH032130A (en) Fluorinated hydrocarbon-based pseudoazeotropic mixture
JPH0317029A (en) Fluorinated hydrocarbon-based solvent composition
JPH0317030A (en) Fluorinated hydrocarbon-based solvent composition
JPH02202830A (en) 1,1-dichloro-2,2,3,3,3-pentafluoropropane-based azeotrope and pseudo azeotrope composition
JPH02204468A (en) Fluorinated hydrocarbon mixed solvent composition
JPH0317031A (en) Fluorinated hydrocarbon-based solvent composition
JPH01141993A (en) Fluorinated hydrocarbon-based azeotropic mixture
JPH02286632A (en) Fluorinated hydrocarbon-based azeotropic composition
JPH02212442A (en) Azeotropic and pseudo-azeotropic mixture of chlorotetrafluoropropane
JPH0331222A (en) Fluorohydrocarbon azeotropic or pseudoazeotropic composition
JPH02286634A (en) Fluorinated hydrocarbon-based azeotropic composition