JPH0491200A - Cleanser composition - Google Patents

Cleanser composition

Info

Publication number
JPH0491200A
JPH0491200A JP20865890A JP20865890A JPH0491200A JP H0491200 A JPH0491200 A JP H0491200A JP 20865890 A JP20865890 A JP 20865890A JP 20865890 A JP20865890 A JP 20865890A JP H0491200 A JPH0491200 A JP H0491200A
Authority
JP
Japan
Prior art keywords
cleaning
alcohol
polyethylene glycol
glycol ester
aliphatic
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.)
Granted
Application number
JP20865890A
Other languages
Japanese (ja)
Other versions
JPH0668118B2 (en
Inventor
Takeshi Kono
武司 河野
Chiaki Wada
千昭 和田
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.)
DKS Co Ltd
Original Assignee
Dai Ichi Kogyo Seiyaku 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 Dai Ichi Kogyo Seiyaku Co Ltd filed Critical Dai Ichi Kogyo Seiyaku Co Ltd
Priority to JP2208658A priority Critical patent/JPH0668118B2/en
Publication of JPH0491200A publication Critical patent/JPH0491200A/en
Publication of JPH0668118B2 publication Critical patent/JPH0668118B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To provide a safe cleanser composition not causing the breakage of the ozone layer and exhibiting an excellent cleansing property by compounding an alkylene oxide adduct of an aliphatic (un)saturated alcohol a higher fatty acid polyethylene glycol ester, etc., in a specific ratio. CONSTITUTION:The objective cleanser composition comprises (A) 60-95 pts.wt. of an alkylene oxide adduct of a 1-4C aliphatic saturated alcohol (e.g. methyl alcohol) and/or a 1-4C aliphatic unsaturated alcohol (e.g. allyl alcohol) and (B) 5-40 pts.wt. of a castor oil polyethylene glycol ester having a HLB of 8-12 and/or 6-22C higher fatty acid polyethylene glycol ester.

Description

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

本発明は、ロジン系フラックス洗浄用洗浄剤組成物に関
するものである。
The present invention relates to a cleaning composition for cleaning rosin-based flux.

【従来の技術】[Conventional technology]

従来のロジン系フラックス洗浄用洗浄剤としては、例え
ばCFC−113に代表される通称フロン溶剤又は1,
1.l−トリクロロエタンに代表される塩素系溶剤が主
として用いられていた。
Conventional rosin-based flux cleaning agents include, for example, commonly known fluorocarbon solvents such as CFC-113, or 1,
1. Chlorinated solvents such as l-trichloroethane have been mainly used.

【発明が解決しようとする課題】[Problem to be solved by the invention]

しかしながら、このような従来のCFC−113或いは
1,1.1−トリクロロエタンにあっては、オゾン層を
破壊する原因物質として厳しい使用削減を計らねばなら
ず、当該洗浄に用いる事か不可能となってきたため、代
替洗浄剤が広く要望されてきている。 代替洗浄には、オゾン破壊係数の少ない或いは無い代替
フロンや、アルコール或いは炭化水素油を主成分とする
水系洗浄剤又はアルカリを主成分とする水系洗浄剤が広
く提案されている。しかしながらこれら代替フロンfc
、浄は、安全性・洗浄性・経済性の点において充分に満
足するレベルには到っておらず、アルコール(系)洗浄
は引火点の低い事より操業安全性に懸念が残り、炭化水
素油を主体とする水系洗浄又はアルカリを圧体とする水
系洗浄剤は被洗浄素材選択性すなわち被洗浄素材への影
響が懸念されるという問題点があった。
However, as conventional CFC-113 or 1,1,1-trichloroethane is a substance that destroys the ozone layer, strict measures must be taken to reduce its use, making it impossible to use it for cleaning. As a result, there has been a wide demand for alternative cleaning agents. As alternative cleaning methods, alternative chlorofluorocarbons with low or no ozone depletion coefficients, water-based detergents containing alcohol or hydrocarbon oil as a main component, or aqueous detergents containing alkali as a main component have been widely proposed. However, these alternative CFC fc
However, alcohol cleaning has not reached a fully satisfactory level in terms of safety, cleaning efficiency, and economic efficiency, and concerns remain about operational safety due to the low flash point of alcohol (based) cleaning, and hydrocarbon cleaning Water-based cleaning agents mainly containing oil or aqueous cleaning agents containing alkali as a pressurizer have a problem in that there is concern about the selectivity of the material to be cleaned, that is, the influence on the material to be cleaned.

【課題を解決するための手段】[Means to solve the problem]

二の発明は、このような従来の問題点に着目してなされ
たものである。すなわち、−炭素数1〜4の脂肪族飽和
アルコール及び/又は炭素数1〜4の脂肪族不飽和アル
コールのアルキレンオキシド付加物を60重量部〜95
重量部と、HLB8〜12のヒマシ油ポリエチレングリ
コールエステル及び/又は炭素数6〜22の高級脂肪酸
ポリエチレングリコールエステルを5重量部〜40重量
部からなることを特徴とする洗浄剤組成物である。 (手段を構成する要件) 本発明の洗浄剤組成物は、アルコール成分(り下A成分
という)と、エステル型非イオン界面活性剤(以下B成
分という)の混合物である。 A成分として炭素数1〜4の脂肪族飽和アルコール及び
/又は炭素数1〜4の脂肪族不飽和アルコールのアルキ
レンオキシド付加物か使用される。炭素数1〜4の脂肪
族飽和アルコールには、メチルアルコール、エチルアル
コール、プロピルアルコール、ブチルアルコールが挙げ
られ、炭素W91〜4の脂肪族不飽チロアルコールに1
寸、マリ;1アルコール、プロパルギルアルコール等が
挙げられる。 又、上記アルコールに付加合成するアルキレンオキンド
はエチレンオキシド、プロビレシオキンド、ブチレンオ
キシドか挙げられ、その付加モル数は1〜5モルが好ま
しい。そ2′1等アルキLンオキシドは単独或いは併用
付加合成する事も何らさしつかえない。 A成分の配合量としては組成物中60〜95重量部であ
り、60重量部未満或は95重量部を赳えるときは洗浄
液劣化時の洗浄性が劣る。 次にB成分はエステル型非イオン界面活性剤として、H
LB8〜12のヒマシ油のポリエチレングリコールエス
テル及び/又はHLB8〜12の炭素数6〜22の高級
脂肪酸のポリエチレングリコールエステルが使用される
。 炭素数6〜22の高級脂肪酸としては、カプロン酸、ラ
ウリン酸、ステアリン酸、オレイン酸等の単独或いは併
用した高級脂肪酸が挙げらねる。 ポリエチレングリコールエステルは、エチレシオキシド
3〜30モルをヒマシ油及び/又は高級脂肪酸に付加さ
せて製造しても良いし、あるいはエチレンオキシドを先
に重合させ、その後エステル化反応させて製造しても良
い。 B成分の配合量は組成物中5〜40重量部であり、5重
量部未満では劣化時洗浄性が劣り、又4ON量部を越え
たときは洗浄全般に劣る。又B成分のHLBは8〜12
である必要があり、HLBが8未満のときは全般に洗浄
性が劣り、特に劣化時洗浄性が大幅に低下し、又HLB
が12を越えるときは全FI9.に洗浄性か劣る。 本願発明洗浄剤組成物はそのまま或は水に希釈して、浸
漬、超音波、噴霧等の洗浄方式に基づき、ロジン系フラ
ックスの付着した基板の洗浄処理を行う。
The second invention was made by focusing on such conventional problems. That is, - 60 parts by weight to 95 parts by weight of an alkylene oxide adduct of an aliphatic saturated alcohol having 1 to 4 carbon atoms and/or an aliphatic unsaturated alcohol having 1 to 4 carbon atoms;
and 5 parts by weight to 40 parts by weight of castor oil polyethylene glycol ester having an HLB of 8 to 12 and/or higher fatty acid polyethylene glycol ester having 6 to 22 carbon atoms. (Requirements constituting means) The cleaning composition of the present invention is a mixture of an alcohol component (hereinafter referred to as component A) and an ester type nonionic surfactant (hereinafter referred to as component B). As component A, an alkylene oxide adduct of an aliphatic saturated alcohol having 1 to 4 carbon atoms and/or an aliphatic unsaturated alcohol having 1 to 4 carbon atoms is used. Examples of aliphatic saturated alcohols having 1 to 4 carbon atoms include methyl alcohol, ethyl alcohol, propyl alcohol, and butyl alcohol;
Examples include alcohol, alcohol, propargyl alcohol, and the like. The alkylene oxide to be added and synthesized to the above-mentioned alcohol may be ethylene oxide, propylene oxide, or butylene oxide, and the number of moles added is preferably 1 to 5 moles. There is no problem in addition-synthesizing the 2'1-iso-alkylene oxides alone or in combination. The blending amount of component A is 60 to 95 parts by weight in the composition, and if it is less than 60 parts by weight or 95 parts by weight, the cleaning performance when the cleaning liquid deteriorates will be poor. Next, component B is an ester type nonionic surfactant, H
A polyethylene glycol ester of castor oil having an LB of 8 to 12 and/or a polyethylene glycol ester of a higher fatty acid having a carbon number of 6 to 22 and an HLB of 8 to 12 is used. Examples of higher fatty acids having 6 to 22 carbon atoms include higher fatty acids such as caproic acid, lauric acid, stearic acid, and oleic acid, which may be used alone or in combination. Polyethylene glycol ester may be produced by adding 3 to 30 moles of ethylene oxide to castor oil and/or higher fatty acids, or may be produced by first polymerizing ethylene oxide and then carrying out an esterification reaction. . The blending amount of component B is 5 to 40 parts by weight in the composition, and if it is less than 5 parts by weight, the cleaning performance during deterioration will be poor, and if it exceeds 4 parts by weight, the overall cleaning will be poor. Also, the HLB of component B is 8 to 12.
When the HLB is less than 8, the cleaning performance is generally poor, especially when it deteriorates, and the cleaning performance is significantly reduced.
When exceeds 12, the total FI9. Cleanability is poor. The cleaning composition of the present invention may be used as it is or diluted with water to perform a cleaning treatment on a substrate to which rosin-based flux has been adhered based on a cleaning method such as immersion, ultrasonic waves, or spraying.

【作用】[Effect]

本発明洗浄剤組成物は、CFC−113或いは1、l、
l−トリクロロエタン等ロジン系フラックス洗浄用に用
いられる水溶性洗浄剤組成物でオゾン層破壊に原因する
物質を全く含有せず、アルコール系洗浄剤に比較し、高
い引火点を有し取扱いが容易であり且つ、優れた洗浄効
果と寿命を有し、水系洗浄剤に比較し取り扱いが安全且
つ優れた洗浄性と洗浄寿命を有し、更に水洗し易い事で
ファイン化の進む基板に付着するロジン系フラックスの
洗浄が容易となる。
The cleaning composition of the present invention contains CFC-113 or 1,1,
A water-soluble detergent composition used for cleaning rosin-based fluxes such as l-trichloroethane, which does not contain any substances that cause ozone layer depletion, has a higher flash point than alcohol-based detergents, and is easy to handle. A rosin-based product that has superior cleaning effects and longevity, and is safer to handle and has superior cleaning performance and cleaning life compared to water-based cleaning agents.In addition, it is easy to wash with water and adheres to increasingly finer substrates. Cleaning of flux becomes easy.

【実施例】【Example】

効果 −1超1゛洗  ) 油性フラックス付着モデル基板を表−1の各々洗浄剤で
60℃、60秒間超音波洗浄、超音波リンスを行い、乾
燥後、残存フラックスを紫外分光光度法にて測定、以下
式により洗浄(%)を求めた。 洗浄性(%) (但しCFC−113は30℃洗浄とする。)効 例−
2(スプレー洗浄 効果例−1と同様条件にて超音波洗浄に替え、2kg/
cm2圧のスプレー洗浄を行う。評価法は効果例−1と
同様に洗浄性C%)−で示す。 表−1に示す各々洗浄剤組成物中に被洗浄油性フラック
スを20%添加し劣化洗浄液とし、効果例−1と同様操
作を行い劣化洗浄液洗浄効果を測定する。      
    (以下余白)本発明洗浄剤組成物1〜3はいず
れの洗浄性についても優れた効果がある。一方比較洗浄
剤組成物について、 (イ+  [71は超音波及びスプレー洗浄性能ル干の
低下と共に劣化洗浄性の大巾低下が観られる。 (ハ)は、A成分のアルコールの炭素数が大きく、著し
い効果の低下が観られた。 (ニ)は、B成分のHLBが低い為、特に劣化洗浄性に
劣る。 (本)は、B成分のHLBが高い為、全Ejに洗浄性低
下が伺える。 (へ)it−)は、B成分の組成の違いの為、全般に洗
浄性が低下傾向にあり、特に、劣化洗浄性が低い。 (手)は、洗浄性は全般に優れるもののオゾン層破壊原
因物質である。 (ワ)は、引火点が低い事の懸念と共に、劣化時の性能
低下が大きい。 (ヌ)は、スプレー洗浄性能の低さと、劣化時の大巾性
能低下か問題である。 (1し)は、劣化時性能の低下と共にハンダ部分へのエ
ツチング影響が著しく実用的な洗浄に速さない。 【発明の効果ン 本発明洗浄剤組成物は、オゾン層を破壊する原因物質に
該当せず、安全かつ優れた洗浄性を特徴する
Effect -1 super 1゛ cleaning) The oil-based flux attached model board was ultrasonically cleaned and rinsed at 60℃ for 60 seconds with each cleaning agent listed in Table-1, and after drying, the residual flux was measured by ultraviolet spectrophotometry. The cleaning (%) was determined using the following formula. Cleanability (%) (However, CFC-113 should be cleaned at 30°C.) Effectiveness example -
2 (Same conditions as spray cleaning effect example-1, instead of ultrasonic cleaning, 2 kg/
Perform spray cleaning at cm2 pressure. The evaluation method is shown in terms of detergency C%) as in Effect Example-1. 20% of the oil-based flux to be cleaned was added to each of the cleaning agent compositions shown in Table 1 to obtain a deteriorated cleaning liquid, and the same operation as in Effect Example 1 was carried out to measure the cleaning effect of the deteriorated cleaning liquid.
(Hereinafter, blank) Cleaning compositions 1 to 3 of the present invention have excellent effects on all cleaning properties. On the other hand, regarding the comparative detergent compositions, (I + [71] shows a decrease in ultrasonic and spray cleaning performance as well as a large decrease in deterioration and cleaning performance. (C) has a large number of carbon atoms in the alcohol of component A. , a significant decrease in effectiveness was observed. In (d), the HLB of the B component is low, so the deterioration and cleaning performance is particularly poor. In (this), the HLB of the B component is high, so there is a decrease in the cleaning performance for all Ej. Because of the difference in the composition of the B component, the cleaning performance of ()it-) generally tends to decrease, and in particular, the deterioration cleaning performance is low. (Hands) have excellent cleaning properties in general, but they are substances that cause ozone layer depletion. (W) is concerned about its low flash point, and there is a large drop in performance when it deteriorates. (N) is a problem of low spray cleaning performance and a decline in wide width performance when it deteriorates. In case (1), the performance deteriorates when it deteriorates, and the etching effect on the solder portion is significant, making it difficult to perform practical cleaning. [Effects of the Invention] The cleaning composition of the present invention does not fall under the category of substances that destroy the ozone layer, and is characterized by safe and excellent cleaning properties.

Claims (1)

【特許請求の範囲】[Claims]  炭素数1〜4の脂肪族飽和アルコール及び/又は炭素
数1〜4の脂肪族不飽和アルコールのアルキレンオキシ
ド付加物を60重量部〜95重量部と、HLB8〜12
のヒマシ油ポリエチレングリコールエステル及び/又は
炭素数6〜22の高級脂肪酸ポリエチレングリコールエ
ステルを5重量部〜40重量部からなることを特徴とす
る洗浄剤組成物。
60 to 95 parts by weight of an alkylene oxide adduct of an aliphatic saturated alcohol having 1 to 4 carbon atoms and/or an aliphatic unsaturated alcohol having 1 to 4 carbon atoms, and HLB 8 to 12.
A cleaning composition comprising 5 to 40 parts by weight of castor oil polyethylene glycol ester and/or higher fatty acid polyethylene glycol ester having 6 to 22 carbon atoms.
JP2208658A 1990-08-06 1990-08-06 Cleaning composition Expired - Lifetime JPH0668118B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2208658A JPH0668118B2 (en) 1990-08-06 1990-08-06 Cleaning composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2208658A JPH0668118B2 (en) 1990-08-06 1990-08-06 Cleaning composition

Publications (2)

Publication Number Publication Date
JPH0491200A true JPH0491200A (en) 1992-03-24
JPH0668118B2 JPH0668118B2 (en) 1994-08-31

Family

ID=16559904

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2208658A Expired - Lifetime JPH0668118B2 (en) 1990-08-06 1990-08-06 Cleaning composition

Country Status (1)

Country Link
JP (1) JPH0668118B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009149903A (en) * 2006-04-27 2009-07-09 Intezyne Technologies Inc Poly (ethylene glycol) containing chemically different terminal groups

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01291905A (en) * 1988-05-20 1989-11-24 Chichibu Cement Co Ltd Raw material blending system
JPH03227400A (en) * 1989-11-08 1991-10-08 Arakawa Chem Ind Co Ltd Detergent for washing rosin-based soldering flux and washing method of same flux

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01291905A (en) * 1988-05-20 1989-11-24 Chichibu Cement Co Ltd Raw material blending system
JPH03227400A (en) * 1989-11-08 1991-10-08 Arakawa Chem Ind Co Ltd Detergent for washing rosin-based soldering flux and washing method of same flux

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009149903A (en) * 2006-04-27 2009-07-09 Intezyne Technologies Inc Poly (ethylene glycol) containing chemically different terminal groups
JP2011058001A (en) * 2006-04-27 2011-03-24 Intezyne Technologies Inc Poly(ethylene glycol) containing chemically disparate end group

Also Published As

Publication number Publication date
JPH0668118B2 (en) 1994-08-31

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