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JP2797610B2 - Fluorinated chlorinated hydrocarbon-based mixed solvent composition - Google Patents

Fluorinated chlorinated hydrocarbon-based mixed solvent composition

Info

Publication number
JP2797610B2
JP2797610B2 JP2052771A JP5277190A JP2797610B2 JP 2797610 B2 JP2797610 B2 JP 2797610B2 JP 2052771 A JP2052771 A JP 2052771A JP 5277190 A JP5277190 A JP 5277190A JP 2797610 B2 JP2797610 B2 JP 2797610B2
Authority
JP
Japan
Prior art keywords
mixed solvent
solvent composition
chlorinated hydrocarbon
fluorinated chlorinated
based 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.)
Expired - Fee Related
Application number
JP2052771A
Other languages
Japanese (ja)
Other versions
JPH03258734A (en
Inventor
健郎 北村
陽子 宇佐見
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 JP2052771A priority Critical patent/JP2797610B2/en
Publication of JPH03258734A publication Critical patent/JPH03258734A/en
Application granted granted Critical
Publication of JP2797610B2 publication Critical patent/JP2797610B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Extraction Or Liquid Replacement (AREA)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、プリント基板、IC等の電子部品、精密機械
部品、ガラス基板等のフラックス洗浄や付着水除去等に
用いられる混合溶剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a mixed solvent composition used for flux cleaning and removing adhering water of printed circuit boards, electronic components such as ICs, precision machine components, glass substrates and the like. .

[従来の技術] フラックス洗浄や付着水除去等には、不燃性、低毒
性、安定性に優れる等の特徴を有する1,1,2−トリクロ
ロ−1,2,2−トリフルオロプロパン(以下R113という)
とアルコールとの混合溶剤組成物が広く使用されてい
る。さらに、R113は金属、プラスチック、エラストマー
等の基材を侵さず、各種の汚れを選択的に溶解する特徴
を有するため、金属、プラスチック、エラストマー等か
らなる各種電子部品を実装したプリント基板のフラック
ス洗浄には最適であった。
[Prior art] 1,1,2-Trichloro-1,2,2-trifluoropropane (hereinafter referred to as R113) having features such as nonflammability, low toxicity, and excellent stability is used for flux washing and removal of attached water. That)
Mixed solvent compositions of alcohol and alcohol are widely used. Furthermore, since R113 has the feature of selectively dissolving various stains without attacking the base materials such as metals, plastics and elastomers, flux cleaning of printed circuit boards mounted with various electronic components made of metals, plastics, elastomers, etc. It was perfect for

[発明が解決しようとする課題] 従来使用されていたR113は、種々の利点を有するにも
かかわらず、化学的に特に安定なため、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、その使用規
制が実施されることとなった。このため、従来のR113に
替わり、オゾン層を破壊しにくい代替溶剤の探索が活発
に行なわれている。
[Problem to be Solved by the Invention] R113, which has been used conventionally, has various advantages, but is particularly stable chemically, so that it has a long life in the troposphere, diffuses into the stratosphere, Here, chlorine radicals generated by decomposition by sunlight cause a chain reaction with ozone and destroy the ozone layer, so that the use of the ozone layer has been restricted. For this reason, instead of the conventional R113, the search for alternative solvents that are less likely to destroy the ozone layer is being actively conducted.

本発明は、従来のR113が有している優れた特性を満足
しながら代替溶剤として使用できる新規なフッ素化塩素
化炭化水素系混合溶剤組成物の提供を目的とする。
An object of the present invention is to provide a novel fluorinated chlorinated hydrocarbon-based mixed solvent composition which can be used as a substitute solvent while satisfying the excellent properties of the conventional R113.

[課題を解決するための手段] 本発明は前述の目的を達成すべくなされたものであ
り、炭素数が3である特定のフッ素化塩素化炭化水素と
2−プロパノールからなる混合物を含む混合溶剤組成
物、を提供する。
Means for Solving the Problems The present invention has been achieved to achieve the above-mentioned object, and a mixed solvent containing a mixture of a specific fluorinated chlorinated hydrocarbon having 3 carbon atoms and 2-propanol A composition.

本発明におけるフッ素化塩素化炭化水素は、3,3−ジ
クロロ−1,1,1,2,2−ペンタフルオロプロパン(CF3CF2C
HCl2、以下R225caという)及び1,3−ジクロロ−1,1,2,
2,3−ペンタフルオロプロパン(CClF2CF2CHClF、以下R2
25cbという)であり、R225caとR225cbとの組成比は特に
限定されないが、好ましくは、R225caが0.01〜99.99重
量%、R225cbが0.01〜99.99重量%である。
The fluorinated chlorinated hydrocarbon in the present invention is 3,3-dichloro-1,1,1,2,2-pentafluoropropane (CF 3 CF 2 C
HCl 2 , hereinafter R225ca) and 1,3-dichloro-1,1,2,
2,3-pentafluoropropane (CClF 2 CF 2 CHClF, hereinafter R2
25 cb), and the composition ratio of R225ca to R225cb is not particularly limited, but preferably, R225ca is 0.01 to 99.99% by weight and R225cb is 0.01 to 99.99% by weight.

フッ素化塩素化炭化水素と2−プロパノールとの混合
組成比は、フッ素化塩素化炭化水素50〜99重量%と2−
プロパノール1〜50重量%である。
The mixture composition ratio of the fluorinated chlorinated hydrocarbon and 2-propanol is 50 to 99% by weight of the fluorinated chlorinated hydrocarbon and 2-
It is 1 to 50% by weight of propanol.

2−プロパノールの含有量が多いほど洗浄性は高くな
るが、2−プロパノールの含有量が50重量%を超えると
混合溶剤組成物が可燃性となる。
The higher the content of 2-propanol, the higher the detergency, but if the content of 2-propanol exceeds 50% by weight, the mixed solvent composition becomes flammable.

本発明の組成物には、必要に応じてその他の成分を更
に添加混合できる。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、n−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、プロパルギルアルコール等のアルコール類、フェ
ノール、o−クレゾール、m−クレゾール、p−クレゾ
ール、2,6−ジ−t−ブチル−p−クレゾール、ビスフ
ェノールA等のフェノール類、メチルセロソルブ、テト
ラヒドロフラン、1,4−ジオキサン、ブチルグリシジル
エーテル、1,2−ジメトキシメタン等のエーテル類、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、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、ジイソプロピルアミン、ジアリルアミン等の
アミン類、酢酸エチル、酢酸プロピル、酢酸ブチル、サ
リチル酸メチル等のエステル類、α−アミレン、β−ア
ミレン等のアミレン類、トリフェニルホスファイト、ト
リブチルホスファイト等の有機ホスファイト類、1,2−
ブチレンオキシド、エピクロルヒドリン等のエポキシド
類、1,2,3−ベンゾトリアゾール、2−(2′−ヒドロ
キシ−5′−メチル−フェニル)ベンゾトリアゾール等
のベンゾトリアゾール類、ジクロロメタン、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−ジクロロ−1−フルオロエタン、1,1−ジクロロ−
1,2,2,3,3−ペンタフルオロプロパン、1,2−ジクロロ−
1,1,3,3,3−ペンタフルオロプロパン、1,1−ジクロロ−
2,3,3,3−テトラフルオロプロペン−1、trans−3−ク
ロロ−1,1,1,2,4,4,5,5,5−ノナフルオロペンテン−
2、cis−3−クロロ−1,1,1,2,4,4,5,5,5−ノナフルオ
ロペンテン−2、1,1,1,2,2,5,5,6,6,6−デカフルオロ
ヘキサン等の、本発明におけるフッ素化塩素化炭化水素
以外のフロン類等を適宜添加できる。
Other components can be further added to and mixed with the composition of the present invention as needed. For example, in the use as a solvent, pentane, isopentane, hexane, isohexane, neohexane, heptane, isoheptane, 2,3-dimethylbutane, hydrocarbons such as cyclopentane, n-propyl alcohol, n-butyl alcohol, i Alcohols such as -butyl alcohol, s-butyl alcohol, t-butyl alcohol, propargyl alcohol, phenol, o-cresol, m-cresol, p-cresol, 2,6-di-t-butyl-p-cresol, bisphenol A, such as phenols, methyl cellosolve, tetrahydrofuran, 1,4-dioxane, butyl glycidyl ether, ethers such as 1,2-dimethoxymethane, ketones such as acetone, methyl ethyl ketone, methyl butyl ketone, nitromethane, nitroethane, nitro Nitroalkanes such as lopan, amines such as diethylamine, triethylamine, isopropylamine, butylamine, isobutylamine, diisopropylamine and diallylamine; esters such as ethyl acetate, propyl acetate, butyl acetate and methyl salicylate; α-amylene, β- Amylenes such as amylene, organic phosphites such as triphenyl phosphite and tributyl phosphite, 1,2-
Epoxides such as butylene oxide and epichlorohydrin, benzotriazoles such as 1,2,3-benzotriazole and 2- (2'-hydroxy-5'-methyl-phenyl) benzotriazole, dichloromethane, trans-1,2
-Dichloroethylene, cis-1,2-dichloroethylene, 2
-Halogenated hydrocarbons such as bromopropane, and others,
1,1-dichloro-1-fluoroethane, 1,1-dichloro-
1,2,2,3,3-pentafluoropropane, 1,2-dichloro-
1,1,3,3,3-pentafluoropropane, 1,1-dichloro-
2,3,3,3-tetrafluoropropene-1, trans-3-chloro-1,1,1,2,4,4,5,5,5-nonafluoropentene-
2, cis-3-chloro-1,1,1,2,4,4,5,5,5-nonafluoropentene-2,1,1,1,2,2,5,5,6,6, Freon other than the fluorinated chlorinated hydrocarbon in the present invention, such as 6-decafluorohexane, can be appropriately added.

これらの成分の添加量は特に限定されないが、溶解力
を調整する場合には、好ましくは1〜50重量%、さらに
好ましくは1〜40重量%程度であり、安定剤として添加
する場合には、好ましくは1ppm〜10重量%、さらに好ま
しくは1ppm〜3重量%程度である。
The addition amount of these components is not particularly limited, but is preferably about 1 to 50% by weight, more preferably about 1 to 40% by weight when adjusting the dissolving power, and when adding as a stabilizer, Preferably it is about 1 ppm to 10% by weight, more preferably about 1 ppm to 3% by weight.

本発明のフッ素化塩素化炭化水素系混合溶剤組成物
は、従来のR113/アルコール系と同程度の溶解力を有す
るため、溶剤等の各種用途に好適に使用できる。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。
Since the fluorinated chlorinated hydrocarbon-based mixed solvent composition of the present invention has the same dissolving power as that of the conventional R113 / alcohol-based mixed solvent composition, it can be suitably used for various uses such as a solvent. Specific applications of the solvent include flux, grease, oil, wax, remover for ink, solvent for paint, extractant, glass, ceramics, plastic, rubber, various metal articles, especially IC parts, electric equipment, Examples of the cleaning agent include a precision machine, a cleaning agent for an optical lens, and a draining agent. Cleaning methods include hand wiping, dipping, spraying, rocking, ultrasonic cleaning,
Steam cleaning or the like may be employed.

[実施例] 「実施例1〜3」 第1表に示す混合溶剤組成物を用いてフラックスの洗
浄試験を行なった。ガラスエポキシ製のプリント基板
(50mm×100mm×1.6mm)全面にフラックス(スピーディ
フラックスAGF−J−I:アサヒ化学研究所製)を塗布
し、250℃の電気炉で2分間焼成後、本発明の混合溶剤
組成物に1分間浸漬した。フラックスの除去の度合
(◎:良好に除去可、△:微量残存、×:かなり残
存。)を第1表に示す。
[Examples] "Examples 1 to 3" Flux washing tests were performed using the mixed solvent compositions shown in Table 1. A flux (speedy flux AGF-JI: manufactured by Asahi Chemical Laboratory) is applied to the entire surface of a printed board made of glass epoxy (50 mm × 100 mm × 1.6 mm) and baked in an electric furnace at 250 ° C. for 2 minutes. It was immersed in the mixed solvent composition for 1 minute. Table 1 shows the degree of flux removal (A: good removal possible, Δ: trace remaining, ×: considerable remaining).

「実施例4〜6」 第2表に示す混合溶剤組成物を用いて付着水の除去試
験を行なった。30mm×18mm×5mmのガラス板を純水に浸
漬後、本発明の混合溶剤組成物中に20秒浸漬して水切り
を行ない、取り出したガラス板を無水メタノール中に浸
漬してメタノール中の水分増加量から付着水の除去状況
を調べた。付着水の除去の度合(◎:良好に除去可、
△:微量残存、×:かなり残存。)を第2表に示す。
"Examples 4 to 6" Using the mixed solvent compositions shown in Table 2, an attached water removal test was performed. After immersing a glass plate of 30 mm x 18 mm x 5 mm in pure water, immersing the glass plate in the mixed solvent composition of the present invention for 20 seconds to perform drainage, and immersing the removed glass plate in anhydrous methanol to increase the water content in methanol. The removal status of the attached water was examined from the amount. Degree of removal of adhering water (◎: good removal possible,
Δ: trace amount remaining, ×: considerably remaining. ) Are shown in Table 2.

「実施例7〜9」 第3表に示す混合溶剤組成物を用いて機械油の洗浄試
験を行なった。SUS−304のテストピース(25mm×30mm×
2mm)を機械油(日本石油製CQ−30)中に浸漬した後、
本発明の混合溶剤組成物中に5分浸漬した。機械油の除
去の度合(◎:良好に洗浄可、△:微量残存、×:かな
り残存。)を第3表に示す。
"Examples 7 to 9" Machine oil cleaning tests were performed using the mixed solvent compositions shown in Table 3. SUS-304 test piece (25mm x 30mm x
2mm) in machine oil (Nippon Oil CQ-30)
It was immersed in the mixed solvent composition of the present invention for 5 minutes. Table 3 shows the degree of removal of the machine oil (A: good cleaning possible, Δ: trace amount remaining, ×: considerable amount remaining).

「実施例10」 R225ca/R225cb/2−プロパノール=30重量%/35重量%
/35重量%についてタグ式引火点測定装置(JIS−K226
5)を用いて、引火点を測定した。その結果、本発明の
混合溶剤組成物は引火点がなく、不燃であることが確認
された。
"Example 10" R225ca / R225cb / 2-propanol = 30% by weight / 35% by weight
Tag type flash point measuring device (JIS-K226
The flash point was measured using 5). As a result, it was confirmed that the mixed solvent composition of the present invention had no flash point and was nonflammable.

[発明の効果] 本発明のフッ素化塩素化炭化水素系混合溶剤組成物
は、従来のR113/アルコール系混合溶剤組成物が有して
いる優れた特性を満足し、従来のR113/アルコール系混
合溶剤組成物と同じ使い方ができ、従来技術の大幅な変
更を要しない等の利点がある。
[Effect of the Invention] The fluorinated chlorinated hydrocarbon-based mixed solvent composition of the present invention satisfies the excellent properties of the conventional R113 / alcohol-based mixed solvent composition, It has the advantages that it can be used in the same manner as the solvent composition and does not require a significant change in the prior art.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI (C11D 7/60 7:30 7:26) (56)参考文献 特開 平2−286630(JP,A) 特開 平2−286631(JP,A) 特開 平2−311430(JP,A) 特開 平3−2129(JP,A) 特開 平3−2130(JP,A) 特開 平3−74338(JP,A) 特開 平3−99029(JP,A) 特開 平3−99030(JP,A) 特開 平3−123744(JP,A) 特開 平3−123745(JP,A) (58)調査した分野(Int.Cl.6,DB名) C07C 19/10 B01D 12/00 C11D 7/50──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification symbol FI (C11D 7/60 7:30 7:26) (56) References JP-A-2-286630 (JP, A) JP-A-2 JP-A-286631 (JP, A) JP-A-2-311430 (JP, A) JP-A-3-2129 (JP, A) JP-A-3-2130 (JP, A) JP-A-3-74338 (JP, A) JP-A-3-99029 (JP, A) JP-A-3-99030 (JP, A) JP-A-3-123744 (JP, A) JP-A-3-123745 (JP, A) Field (Int.Cl. 6 , DB name) C07C 19/10 B01D 12/00 C11D 7/50

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】3,3−ジクロロ−1,1,1,2,2−ペンタフルオ
ロプロパン、1,3−ジクロロ−1,1,2,2,3−ペンタフルオ
ロプロパン及び2−プロパノールからなる混合物であっ
て、3,3−ジクロロ−1,1,1,2,2−ペンタフルオロプロパ
ン及び1,3−ジクロロ−1,1,2,2,3−ペンタフルオロプロ
パンの合量が50〜99重量%でありかつ2−プロパノール
が1〜50重量%である混合物を含むフッ素化塩素化炭化
水素系混合溶剤組成物。
(1) Consisting of 3,3-dichloro-1,1,1,2,2-pentafluoropropane, 1,3-dichloro-1,1,2,2,3-pentafluoropropane and 2-propanol A mixture, wherein the total amount of 3,3-dichloro-1,1,1,2,2-pentafluoropropane and 1,3-dichloro-1,1,2,2,3-pentafluoropropane is 50 to 50. A fluorinated chlorinated hydrocarbon-based mixed solvent composition comprising a mixture of 99% by weight and 1 to 50% by weight of 2-propanol.
JP2052771A 1990-03-06 1990-03-06 Fluorinated chlorinated hydrocarbon-based mixed solvent composition Expired - Fee Related JP2797610B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2052771A JP2797610B2 (en) 1990-03-06 1990-03-06 Fluorinated chlorinated hydrocarbon-based mixed solvent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2052771A JP2797610B2 (en) 1990-03-06 1990-03-06 Fluorinated chlorinated hydrocarbon-based mixed solvent composition

Publications (2)

Publication Number Publication Date
JPH03258734A JPH03258734A (en) 1991-11-19
JP2797610B2 true JP2797610B2 (en) 1998-09-17

Family

ID=12924131

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2052771A Expired - Fee Related JP2797610B2 (en) 1990-03-06 1990-03-06 Fluorinated chlorinated hydrocarbon-based mixed solvent composition

Country Status (1)

Country Link
JP (1) JP2797610B2 (en)

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2734624B2 (en) * 1989-04-26 1998-04-02 旭硝子株式会社 Fluorinated hydrocarbon-based azeotropic compositions
JPH03123744A (en) * 1989-10-06 1991-05-27 Asahi Glass Co Ltd Fluorinated hydrocarbon azeotropic composition and azeotropic-like composition
JP2780374B2 (en) * 1989-09-12 1998-07-30 旭硝子株式会社 Fluorinated hydrocarbon azeotropic compositions
JPH03123745A (en) * 1989-10-06 1991-05-27 Asahi Glass Co Ltd Fluorinated hydrocarbon azeotropic composition and azeotropic-like composition
JP2737250B2 (en) * 1989-05-30 1998-04-08 旭硝子株式会社 Fluorinated hydrocarbon pseudoazeotrope
JP2734623B2 (en) * 1989-04-26 1998-04-02 旭硝子株式会社 Fluorinated hydrocarbon-based azeotropic compositions
JP2780364B2 (en) * 1989-08-14 1998-07-30 旭硝子株式会社 Fluorinated hydrocarbon azeotropic compositions
JP2792134B2 (en) * 1989-09-12 1998-08-27 旭硝子株式会社 Fluorinated hydrocarbon azeotropic compositions
JP2737249B2 (en) * 1989-05-30 1998-04-08 旭硝子株式会社 Fluorinated hydrocarbon pseudoazeotrope
JP2737246B2 (en) * 1989-05-26 1998-04-08 旭硝子株式会社 Fluorinated hydrocarbon azeotropic compositions

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Publication number Publication date
JPH03258734A (en) 1991-11-19

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