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JPS5910758B2 - azeotropic solvent composition - Google Patents

azeotropic solvent composition

Info

Publication number
JPS5910758B2
JPS5910758B2 JP7261680A JP7261680A JPS5910758B2 JP S5910758 B2 JPS5910758 B2 JP S5910758B2 JP 7261680 A JP7261680 A JP 7261680A JP 7261680 A JP7261680 A JP 7261680A JP S5910758 B2 JPS5910758 B2 JP S5910758B2
Authority
JP
Japan
Prior art keywords
azeotropic
composition
solvent
azeotropic solvent
solvent composition
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
Application number
JP7261680A
Other languages
Japanese (ja)
Other versions
JPS56167800A (en
Inventor
巌 久本
知明 前田
幸雄 大牟礼
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.)
Daikin Industries Ltd
Original Assignee
Daikin Kogyo 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 Daikin Kogyo Co Ltd filed Critical Daikin Kogyo Co Ltd
Priority to JP7261680A priority Critical patent/JPS5910758B2/en
Priority to US06/253,390 priority patent/US4378303A/en
Priority to GB8111641A priority patent/GB2076009B/en
Priority to DE3115015A priority patent/DE3115015C2/en
Publication of JPS56167800A publication Critical patent/JPS56167800A/en
Publication of JPS5910758B2 publication Critical patent/JPS5910758B2/en
Expired legal-status Critical Current

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  • Manufacturing Of Printed Wiring (AREA)
  • Detergent Compositions (AREA)

Description

【発明の詳細な説明】 本発明は新規な共沸溶剤組成物とくにアトラグ −ロロ
ジフルオロエタン、炭素数4のアルコールおよびニトロ
エタンから成る共沸溶剤組成物に係る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to novel azeotropic solvent compositions, particularly azeotropic solvent compositions comprising atlag-rollodifluoroethane, a C4 alcohol, and nitroethane.

クロロフルオロエタン溶剤は、平然性で、毒性が小さい
他に、高分子物質例えばゴムやプラスチックなどよりな
る被洗浄材を侵すことなく油脂、 。グリースなどを溶
解するという選択的溶解性能にすぐれる等、種々の利点
を有している。最近、例えば電子工業界などにおけるプ
リント基板の高融点ロジンフラックス、その他高融点グ
リースや油脂類を洗浄除去するために、化学的に 。
Chlorofluoroethane solvent is non-toxic, has low toxicity, and can be used to clean oils and fats without attacking materials to be cleaned made of polymeric substances such as rubber and plastics. It has various advantages such as excellent selective dissolving performance for dissolving grease and the like. Recently, chemical methods have been used to clean and remove high-melting point rosin flux, other high-melting point greases, and oils from printed circuit boards, such as in the electronics industry.

安定、かつ安全な比較的高沸点のフロン系溶媒の出現が
望まれている。フロン系溶媒のうち、トリクロロトリフ
ルオロエタンは化学的安定性および作業性の点でもつと
もすぐれているが、溶解性能が十分満足なものでなく、
さらには低沸点(47.6℃)であることから、前記の
要望を満たすことは本質的に不可能である。
It is desired that a stable and safe fluorocarbon solvent with a relatively high boiling point be developed. Among chlorofluorocarbon solvents, trichlorotrifluoroethane has excellent chemical stability and workability, but its dissolution performance is not fully satisfactory.
Furthermore, since it has a low boiling point (47.6° C.), it is essentially impossible to satisfy the above requirements.

一方、テトラクロロジフルオロエタンはトリクロロトリ
フルオロエタンに比べ溶解性能がすぐれ、また高沸点(
92.8℃)であるため、前記高融点汚染物を溶解する
ことができるが、十分な化学的安定性に欠け、また高融
点(26、O℃)であるためその使用が制限されている
のが実情である。
On the other hand, tetrachlorodifluoroethane has better solubility than trichlorotrifluoroethane and has a higher boiling point (
92.8°C), which makes it possible to dissolve the high melting point contaminants, but its use is limited because it lacks sufficient chemical stability and has a high melting point (26,0°C). That is the reality.

従来、テトラクロロジフルオロエタン(以下、フロン1
12という)の融点を低下させる目的で、他の有機溶剤
を組合せる方法が数多く提案されている。しかし、この
ような方法の多くは、プロソー112の前記有用な性質
や化学的安定性を損なうか、またはそのような混合溶剤
の多くは共沸組成を形成しないため一般に実用的でない
。ところで、今までプロソーl 12の化学的安定性を
向上せしめ、融点を低下させるもつとも有利な方法とし
て、プロソー112、アルコール類およびニトロメタン
より成る共沸溶剤組成物が知られている(特公昭53−
1232)。
Conventionally, tetrachlorodifluoroethane (hereinafter referred to as Freon 1)
For the purpose of lowering the melting point of 12), many methods have been proposed in which other organic solvents are combined. However, many such methods are generally impractical because they impair the useful properties and chemical stability of Proso 112, or because many such mixed solvents do not form azeotropic compositions. By the way, an azeotropic solvent composition consisting of Prosol 112, an alcohol, and nitromethane has been known as an extremely advantageous method for improving the chemical stability of Prosol 112 and lowering its melting point (Japanese Patent Publication No. 1983-1999).
1232).

しかし、この共沸組成物はプロソー112の安定化に必
要な量よりも大過剰のニトロメタンを使用するため、被
洗浄材、例えば、ゴムやプラスチックの材質を侵す危険
があり、さらには毒性や価格の面でも不利益をまぬがれ
得ない。本発明者らはテトラクロロジフルオロエタンの
前記溶剤としての特色を生かし化学的不安定性、高融点
などの欠点を解消し、さらに前述のごとき材質に対して
も安全な、その他種々の利点を有する新しい共沸溶剤組
成物を見出すに至り、本発明を完成した。即ち、本発明
はテトラクロロジフルオロエタン89.0〜64.6重
量%、炭素数4のアルコール3.7〜34.2重量%お
よびニトロエタン7.3〜1.2重量%から成る共沸溶
剤組成物に係るものである。
However, since this azeotropic composition uses a large excess of nitromethane than is necessary to stabilize Proso 112, there is a risk of attacking the materials to be cleaned, such as rubber and plastics, and furthermore, there is a risk of toxicity and price. They cannot avoid being disadvantaged in this respect as well. The present inventors took advantage of the characteristics of tetrachlorodifluoroethane as a solvent to solve its disadvantages such as chemical instability and high melting point, and created a new solvent that is safe for the materials mentioned above and has various other advantages. The present invention was completed by discovering a boiling solvent composition. That is, the present invention provides an azeotropic solvent composition comprising 89.0 to 64.6% by weight of tetrachlorodifluoroethane, 3.7 to 34.2% by weight of alcohol having 4 carbon atoms, and 7.3 to 1.2% by weight of nitroethane. This is related to.

ここに、テトラクロロジフルオロエタン1,12,2−
テトラクロロ−1,2−ジフルオロエタンの単独物の他
、これの異性体である1,1,12−テトラクロロ−2
,2−ジフルオロエタンとの混合物をも含めていうもの
とする。
Here, tetrachlorodifluoroethane 1,12,2-
In addition to tetrachloro-1,2-difluoroethane alone, its isomer 1,1,12-tetrachloro-2
, 2-difluoroethane.

また、炭素数4のアルコールはn−ブチルアルコーノK
,isO−ブチルアルコール、Sec−ブチルアルコー
ルおよびTert−ブチルアルコールをいうものとする
In addition, alcohol with 4 carbon atoms is n-butylalconoK
, isO-butyl alcohol, Sec-butyl alcohol and tert-butyl alcohol.

本発明の共沸溶剤組成物の組成および物性は下記第1表
のとおりである。
The composition and physical properties of the azeotropic solvent composition of the present invention are shown in Table 1 below.

参考のために前記公知例についても同様に併記する。本
発明の組成物によれば、化学的に安定で低毒性の比較的
高沸点の溶媒が提供されるので、プリント基板の高融点
口シッフラックス、その他高融点グリースや油脂類を容
易に洗浄、除去することができる。
For reference, the above-mentioned known examples are also listed in the same manner. According to the composition of the present invention, since a chemically stable, low-toxicity, and relatively high-boiling solvent is provided, it is possible to easily clean high-melting point flux from printed circuit boards, other high-melting point greases, and oils. Can be removed.

またニトロエタンの使用量が少ないので、前記材質等へ
の悪影響が少なく、毒性や価格の面でも有利で、加えて
溶剤としてすぐれる炭素数4のアルコールのため、被洗
浄物への悪影響が比較的少くて溶解性能がアツプすると
いう選択溶解性能がすぐれる。その他本発明組成物は共
沸組成を形成するため、使用時の液管理や溶剤の回収再
使用がきわめて容易である。本発明の共沸組成物は、前
記第1表の組成割合で各成分を任意の順序で加えて混合
することにより、また各成分を任意の割合で混合したも
のを蒸留することによつても製造することができる。
In addition, since the amount of nitroethane used is small, it has less negative impact on the materials mentioned above, and is advantageous in terms of toxicity and cost.In addition, since the alcohol has 4 carbon atoms and is an excellent solvent, it has a relatively low negative impact on the items being cleaned. It has excellent selective dissolution performance, which improves dissolution performance even with a small amount. In addition, since the composition of the present invention forms an azeotropic composition, liquid management during use and solvent recovery and reuse are extremely easy. The azeotropic composition of the present invention can be prepared by adding and mixing each component in any order in the composition ratios shown in Table 1, or by distilling a mixture of each component in any ratio. can be manufactured.

本発明の共沸溶剤組成物は、前記プリント基板のフラツ
クス洗浄の他、眼鏡フレームの研磨後の洗浄、水溶性切
削油を使用して切削した被切削物の洗浄等にも広範囲に
亘つて有効に用いられる。つぎに実施例および実験例を
挙げて本発明の共沸溶剤組成物について説明する。実施
例 1 下記第2表の組成からなる溶剤混合物5009を蒸留フ
ラスコに入れ、理論段数30段の精留塔を用いて常圧下
に蒸留を行なつた。
The azeotropic solvent composition of the present invention is effective over a wide range of purposes, such as cleaning the flux of printed circuit boards, cleaning eyeglass frames after polishing, and cleaning workpieces cut using water-soluble cutting oil. used for. Next, the azeotropic solvent composition of the present invention will be explained with reference to Examples and Experimental Examples. Example 1 Solvent mixture 5009 having the composition shown in Table 2 below was placed in a distillation flask and distilled under normal pressure using a rectification column having 30 theoretical plates.

その結果、88.7℃において最低共沸点を示した。As a result, the lowest azeotropic point was shown at 88.7°C.

また第2表に於いてn−ブチルアルコールに替えて、I
sO−ブチルアルコール. Sec−ブチルアルコール
、Tert−ブチルアルコールを夫々使用した場合は、
夫々、108.3℃、98.8℃、82.9℃の最低共
沸点を示した。これ等夫々の留分をガスクロマトグラフ
イ一により分析した結果、第2表に示す組成のものであ
つた。実験例 1 実施例1で得られた各共沸溶剤組成物が高融点フラツク
スの洗浄に適するものであるかどうかを調らべるために
次の実験を行なつた。
Also, in Table 2, instead of n-butyl alcohol, I
sO-butyl alcohol. When Sec-butyl alcohol and tert-butyl alcohol are used,
The lowest azeotropic points were 108.3°C, 98.8°C, and 82.9°C, respectively. As a result of analyzing each of these fractions by gas chromatography, they had the compositions shown in Table 2. Experimental Example 1 The following experiment was conducted to examine whether each of the azeotropic solvent compositions obtained in Example 1 was suitable for cleaning high melting point fluxes.

フエノール樹脂銅張積層板よりなるプリント基板(60
關×50m0全面に次表に示すプレフラツクスを塗布し
、ついでポストフラツクスを塗布した後、約250℃で
2分間焼成した。
Printed circuit board made of phenolic resin copper-clad laminate (60
A pre-flux shown in the following table was applied to the entire surface of the 50 m area, and then a post-flux was applied, followed by firing at about 250°C for 2 minutes.

この基板を室温まで冷却したのち、ビーカ中に入れられ
た前記各溶剤組成物300m1中に浸漬した。
After this substrate was cooled to room temperature, it was immersed in 300 ml of each of the above-mentioned solvent compositions placed in a beaker.

フラツクスの除去程度を肉眼で観察し、その結果を次表
を示す。
The degree of flux removal was visually observed and the results are shown in the table below.

実験例 2 実施例1で得られた共沸溶剤組成物がプラスチツクより
なる被洗浄材の材質を浸さないで研磨材の除去にすぐれ
た効果があることを調べるために次の実験を行なつた。
Experimental Example 2 The following experiment was conducted to find out that the azeotropic solvent composition obtained in Example 1 has an excellent effect on removing abrasives without soaking the material to be cleaned, which is made of plastic. .

通常用いられるハブ研磨装置の布面に、研磨材として白
棒(アルミナ、ケイ砂などを油脂と練り合せたもの)を
塗りつけ、アセチルセルロースよりなる眼鏡フレームの
研磨を行なつた。
A white rod (a mixture of alumina, silica sand, etc. mixed with oil and fat) was applied as an abrasive to the cloth surface of a commonly used hub polisher to polish an eyeglass frame made of cellulose acetate.

Claims (1)

【特許請求の範囲】[Claims] 1 テトラクロロジフルオロエタン89.0〜64.6
重量%、炭素数4のアルコール3.7〜34.2重量%
およびニトロエタン7.3〜1.2重量%から成る共沸
溶剤組成物。
1 Tetrachlorodifluoroethane 89.0-64.6
Weight%, carbon number 4 alcohol 3.7-34.2% by weight
and an azeotropic solvent composition consisting of 7.3 to 1.2% by weight of nitroethane.
JP7261680A 1980-04-14 1980-05-29 azeotropic solvent composition Expired JPS5910758B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP7261680A JPS5910758B2 (en) 1980-05-29 1980-05-29 azeotropic solvent composition
US06/253,390 US4378303A (en) 1980-04-14 1981-04-13 Azeotropic solvent composition
GB8111641A GB2076009B (en) 1980-04-14 1981-04-13 Azeotropic solvent composition
DE3115015A DE3115015C2 (en) 1980-04-14 1981-04-14 Azeotropic mixed solvents

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7261680A JPS5910758B2 (en) 1980-05-29 1980-05-29 azeotropic solvent composition

Publications (2)

Publication Number Publication Date
JPS56167800A JPS56167800A (en) 1981-12-23
JPS5910758B2 true JPS5910758B2 (en) 1984-03-10

Family

ID=13494485

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7261680A Expired JPS5910758B2 (en) 1980-04-14 1980-05-29 azeotropic solvent composition

Country Status (1)

Country Link
JP (1) JPS5910758B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5960439B2 (en) * 2012-01-27 2016-08-02 スリーエム イノベイティブ プロパティズ カンパニー Dust removal cleaning liquid and cleaning method using the same

Also Published As

Publication number Publication date
JPS56167800A (en) 1981-12-23

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