JPH07138595A - Detergent - Google Patents

Detergent

Info

Publication number
JPH07138595A
JPH07138595A JP31256493A JP31256493A JPH07138595A JP H07138595 A JPH07138595 A JP H07138595A JP 31256493 A JP31256493 A JP 31256493A JP 31256493 A JP31256493 A JP 31256493A JP H07138595 A JPH07138595 A JP H07138595A
Authority
JP
Japan
Prior art keywords
weight
cleaning agent
detergent
agent according
cleaning
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
JP31256493A
Other languages
Japanese (ja)
Inventor
Masao Fukuda
政雄 福田
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.)
Sanyo Chemical Industries Ltd
Original Assignee
Sanyo Chemical Industries 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 Sanyo Chemical Industries Ltd filed Critical Sanyo Chemical Industries Ltd
Priority to JP31256493A priority Critical patent/JPH07138595A/en
Publication of JPH07138595A publication Critical patent/JPH07138595A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents

Abstract

PURPOSE:To obtain a halogen-free detergent having a detergency for various stains which is comparable to those of chlorinated hydrocarbon solvents, by using a specific glycol monoester compd. or an etherification or esterification product thereof. CONSTITUTION:(A) at least one of glycol monoester compds. prepd. by polymn. of 3 molecules of at least one 2-6C aliph. aldehyde, and etherification or esterification products thereof is blended in a detergent. It is pref. that at least 10wt.% component (A) be blended with (B) at most 90wt.% glycol ether compd. It is also pref. that at least 10wt.% component (A) be blended with at most 50wt.% water and, if necessary, (C) at most 20wt.% surfactant. It is further pref. that at least 10wt.% component (A) be blended with (D) a hydrocarbon solvent in an amt. of at most 90wt.% based on (A)+(D). Additionally stated, in the case of (A), (A)+(B), (A)+ water, or (A)+ water +(C), the aliph. aldehyde is pref. acetaldehyde, propionaldehyde, or the like.

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、金属加工品、電子部
品、光学部品、樹脂成形品、印刷版等の被洗浄物の表面
に存在する指紋、油脂、機械油、切削油、グリース、ワ
ックス、液晶、ロジン系フラックス、印刷インキ、金属
粉、塵埃等の汚れの除去性に優れる非ハロゲン系洗浄剤
組成物に関する。
FIELD OF THE INVENTION The present invention relates to fingerprints, oils and fats, machine oils, cutting oils, greases and waxes present on the surface of objects to be cleaned such as metalworked products, electronic parts, optical parts, resin molded products and printing plates. The present invention relates to a non-halogen type cleaning composition having excellent removability of stains such as liquid crystal, rosin-based flux, printing ink, metal powder and dust.

【0002】[0002]

【従来の技術】従来より機械金属類、電気製品、電子部
品、光学部品、樹脂成形品等の表面に付着した機械油、
グリース、フラックス、ワックス、インキ、指紋などの
有機系の汚れや金属、ガラスなどの微粉などの汚れを除
去するための洗浄剤としては、トリクロルエタン、トリ
クロロトリフルオロエタン等のハロゲン化炭化水素系溶
剤が使用されている。ハロゲン化炭化水素系溶剤は幅広
い汚れを洗浄できるだけでなく、不燃性かつ乾燥性に優
れるなど非常に使いやすい溶剤であるが、これらの中の
いくつかは大気圏のオゾン層を破壊することが判ってい
るなど、環境汚染や安全性の点からこれら溶剤の使用規
制が強化されつつある。それで、これらのハロゲン化炭
化水素系溶剤から非ハロゲン系洗浄剤への代替が産業界
で現在急ピッチで進められており、非ハロゲン系の代替
洗浄剤としては、例えば「オゾン層破壊物質使用削減マ
ニュアル第3版」(オゾン層保護対策産業協議会発行、
1993年5月1日)に記載のアルコール系洗浄剤、炭
化水素系洗浄剤、水系洗浄剤およびその他の洗浄剤が知
られている。
2. Description of the Related Art Conventionally, mechanical oil adhered to the surface of mechanical metals, electric products, electronic parts, optical parts, resin molded products,
As a cleaning agent to remove organic stains such as grease, flux, wax, ink and fingerprints, and stains such as fine powder of metals and glass, halogenated hydrocarbon solvents such as trichloroethane and trichlorotrifluoroethane. Is used. Halogenated hydrocarbon solvents are very easy-to-use solvents that not only clean a wide range of stains but also are non-flammable and dry, but some of these have been found to destroy the ozone layer in the atmosphere. The regulations on the use of these solvents are being tightened from the standpoints of environmental pollution and safety. Therefore, the replacement of these halogenated hydrocarbon solvents with non-halogen detergents is currently being promoted at a rapid pace in the industry, and examples of non-halogen alternative detergents include "reduction of use of ozone-depleting substances. Manual 3rd Edition "(published by the Council for Measures against Ozone Layer Protection,
Alcohol-based cleaning agents, hydrocarbon-based cleaning agents, water-based cleaning agents, and other cleaning agents described in May 1, 1993) are known.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、アルコ
ール系洗浄剤はフラックスの洗浄力は優れているものの
脱脂力においてはトリクロルエタンなどの塩素化炭化水
素系溶剤よりも劣っている。炭化水素系洗浄剤は脱脂力
は優れているが、極性の強い有機系の汚れなどの洗浄に
難点がある。水系洗浄剤は被洗浄物表面にしみや錆が発
生しやすい欠点がある。またその他の代替洗浄剤が現在
開発中であるが、トリクロルエタンなどの塩素化炭化水
素系溶剤と同様に幅広い汚れに対応できる非ハロゲン系
の代替洗浄剤は未だ出現していない。
However, although alcohol-based detergents have excellent flux detergency, they are inferior in degreasing ability to chlorinated hydrocarbon solvents such as trichloroethane. Hydrocarbon-based cleaning agents have excellent degreasing power, but have a difficulty in cleaning highly polar organic stains. The water-based cleaning agent has a drawback that stains and rust are easily generated on the surface of the object to be cleaned. Although other alternative cleaning agents are currently under development, a non-halogen alternative cleaning agent that can deal with a wide range of stains like chlorinated hydrocarbon solvents such as trichloroethane has not yet appeared.

【0004】[0004]

【課題を解決するための手段】本発明者は、塩素化炭化
水素系溶剤と同様に幅広い汚れに対応でき且つ環境汚染
や安全性の問題を改善する非ハロゲン系洗浄剤を得るべ
く鋭意検討した結果、本発明に到達した。すなわち本発
明は、炭素数2〜6の脂肪族アルデヒド1種以上3分子
が重合してなるグリコールモノエステル化合物もしくは
そのエーテル化ないしエステル化物(A)1種以上から
なることを特徴とする洗浄剤である。
Means for Solving the Problems The present inventor diligently studied to obtain a non-halogen type cleaning agent which can deal with a wide range of stains like the chlorinated hydrocarbon type solvent and can improve environmental pollution and safety problems. As a result, the present invention has been reached. That is, the present invention is a detergent comprising a glycol monoester compound obtained by polymerizing one or more kinds of 3 or more molecules of an aliphatic aldehyde having 2 to 6 carbon atoms or one or more kinds of an etherified or esterified product (A) thereof. Is.

【0005】本発明において、炭素数2〜6の脂肪族ア
ルデヒドとしては、例えばアセトアルデヒド、プロピル
アルデヒド、n−ブチルアルデヒド、イソブチルアルデ
ヒド、バレルアルデヒド、イソバレルアルデヒド、カプ
ロンアルデヒド等が挙げられる。本発明において、該グ
リコールモノエステル化合物は例えば炭素数2〜6の脂
肪族アルデヒド1種以上をMg(OC252、Ca
(OC252、Mg[Al(OC2542、Na2
g(OC254等の弱塩基性の配位触媒の存在下で3
分子の重合反応させることにより得られ、その化学式は
次式(1)
In the present invention, examples of the aliphatic aldehyde having 2 to 6 carbon atoms include acetaldehyde, propyl aldehyde, n-butyraldehyde, isobutyraldehyde, valeraldehyde, isovaleraldehyde, capronaldehyde and the like. In the present invention, the glycol monoester compound includes, for example, one or more aliphatic aldehydes having 2 to 6 carbon atoms, Mg (OC 2 H 5 ) 2 , Ca
(OC 2 H 5 ) 2 , Mg [Al (OC 2 H 5 ) 4 ] 2 , Na 2 M
3 in the presence of a weakly basic coordination catalyst such as g (OC 2 H 5 ) 4.
It is obtained by polymerizing a molecule, and its chemical formula is represented by the following formula (1).

【0006】[0006]

【化1】 [Chemical 1]

【0007】(式中、Zは炭素数2〜6の2価の脂肪族
炭化水素基を示し、R1、R2、R3、R4は独立に水素ま
たは炭素数1〜4の脂肪族炭化水素基を示す。)で表す
ことができる。このグリコールモノエステル化合物のエ
ーテル化物としては例えば低級アルキル(炭素数1〜
6)エーテル化物即ちグリコールモノエステルモノエー
テル化合物が挙げられ、エステル化物としては、例えば
酢酸などの低級脂肪酸(炭素数2〜6)エステル化物即
ちグリコールジエステル化合物が挙げられる。これらの
中で(A)として好ましいものはグリコールモノエステ
ル化合物であり、その具体例としては1,3−ブタンジ
オールモノアセテート(アセトアルデヒドの3分子重合
物;沸点210℃)、2−メチル−1,3−ペンタンジ
オールモノプロピオネート(プロピオンアルデヒドの3
分子重合物;沸点235℃)、2−エチル1,3−ヘキ
サンジオールモノブチレート(n−ブチルアルデヒドの
3分子重合物;沸点255℃)、2,2,4−トリメチ
ル−1,3−ペンタンジオールモノイソブチレート(イ
ソブチルアルデヒドの3分子重合物;沸点248℃)等
が挙げられる。(A)の常圧での沸点は、通常150〜
300℃、好ましくは180〜260℃である。沸点が
150℃未満では臭気および引火性が大きくなるので、
作業環境面が悪くなって好ましくない。また、沸点が3
00℃を越えると洗浄後の乾燥性が悪くなるので好まし
くない。
(In the formula, Z represents a divalent aliphatic hydrocarbon group having 2 to 6 carbon atoms, and R 1 , R 2 , R 3 and R 4 are independently hydrogen or an aliphatic group having 1 to 4 carbon atoms. It represents a hydrocarbon group.). Examples of etherification products of this glycol monoester compound include lower alkyl (having 1 to 1 carbon atoms).
6) Ether compounds, that is, glycol monoester monoether compounds, and examples of the ester compounds include lower fatty acid (C2-6) ester compounds such as acetic acid, that is, glycol diester compounds. Among these, preferred as (A) is a glycol monoester compound, and specific examples thereof include 1,3-butanediol monoacetate (a trimolecular polymer of acetaldehyde; boiling point 210 ° C.), 2-methyl-1, 3-Pentanediol monopropionate (3 of propionaldehyde
Molecular polymer; boiling point 235 ° C.), 2-ethyl 1,3-hexanediol monobutyrate (trimolecular polymer of n-butyraldehyde; boiling point 255 ° C.), 2,2,4-trimethyl-1,3-pentane Examples thereof include diol monoisobutyrate (a trimolecular polymer of isobutyraldehyde; boiling point 248 ° C.). The boiling point of (A) at normal pressure is usually 150 to
The temperature is 300 ° C, preferably 180 to 260 ° C. If the boiling point is less than 150 ° C, odor and flammability will increase, so
The work environment is not good, which is not preferable. Also, the boiling point is 3
When the temperature exceeds 00 ° C, the drying property after washing is deteriorated, which is not preferable.

【0008】本発明の洗浄剤の成分として、必要により
(A)と共にグリコールエーテル系化合物(B)を併用
することができる。該グリコールエーテル系化合物
(B)は下記一般式(2)
As a component of the detergent of the present invention, a glycol ether compound (B) can be used together with (A) if necessary. The glycol ether compound (B) has the following general formula (2)

【0009】[0009]

【化2】 [Chemical 2]

【0010】(式中、Yは炭素数2〜4のアルキレン基
を示し、R5は炭素数1〜8の炭化水素基を示し、R6
水素、炭素数1〜8の炭化水素基またはアシル基を示
し、nは1〜4の整数を示す。)で表すことができ、そ
の具体例としては、例えば特開平4−325598号公
報記載の化合物が挙げられる。これらの中では、モノま
たはジエチレングリコールモノアルキル(炭素数1〜
6)エーテル類、モノまたはジプロピレングリコール
(炭素数1〜6)モノアルキルエーテル類、モノまたは
ジエチレングリコールジアルキル(炭素数1〜6)エー
テル類が好ましい。(A)、(B)を併用する場合、本
発明の洗浄剤中の(A)の量は通常10重量%以上であ
り、(B)の量は、通常90重量%以下、好ましくは1
0〜80重量%である。
(In the formula, Y represents an alkylene group having 2 to 4 carbon atoms, R 5 represents a hydrocarbon group having 1 to 8 carbon atoms, R 6 represents hydrogen, a hydrocarbon group having 1 to 8 carbon atoms, or It represents an acyl group, and n represents an integer of 1 to 4.). Specific examples thereof include compounds described in JP-A-4-325598. Among these, mono or diethylene glycol monoalkyl (C1-C1
6) Ethers, mono- or dipropylene glycol (having 1 to 6 carbon atoms) monoalkyl ethers, and mono- or diethylene glycol dialkyl (having 1 to 6 carbon atoms) ethers are preferable. When (A) and (B) are used in combination, the amount of (A) in the detergent of the present invention is usually 10% by weight or more, and the amount of (B) is usually 90% by weight or less, preferably 1%.
It is 0 to 80% by weight.

【0011】本発明の洗浄剤の成分として、(A)およ
び必要により(B)と共に引火性を低くする等の目的で
適当量の水を使用することができる。水を用いる場合、
本発明の洗浄剤中の(A)の量は通常10重量%以上、
(B)の量は通常90重量%以下であり、水の量は通常
50重量%以下、好ましくは0.5〜20重量%であ
る。
As a component of the cleaning agent of the present invention, an appropriate amount of water can be used together with (A) and optionally (B) for the purpose of lowering the flammability. When using water,
The amount of (A) in the cleaning agent of the present invention is usually 10% by weight or more,
The amount of (B) is usually 90% by weight or less, and the amount of water is usually 50% by weight or less, preferably 0.5 to 20% by weight.

【0012】上記のように水を併用する場合、必要によ
り更にアニオン性界面活性剤、カチオン性界面活性剤、
両性界面活性剤、非イオン性界面活性剤などの界面活性
剤(C)1種以上を本発明の洗浄剤の成分として水と共
に使用できる。これら界面活性剤(C)の使用量は、本
発明の洗浄剤の通常20重量%以下、好ましくは0.2
〜10重量%である。
When water is used in combination as described above, an anionic surfactant, a cationic surfactant, and
One or more surfactants (C) such as amphoteric surfactants and nonionic surfactants can be used together with water as a component of the detergent of the present invention. The amount of these surfactants (C) used is usually 20% by weight or less, preferably 0.2% by weight of the detergent of the present invention.
10 to 10% by weight.

【0013】また、本発明の洗浄剤は、(A)と炭化水
素系溶剤(D)を併用したものでもよく、併用により汚
れの対象範囲を広くすることができる。炭化水素系溶剤
(D)としては、ノルマルパラフィン、イソパラフィ
ン、シクロパラフィン、ケロシン、テルペンなどの脂肪
族炭化水素系溶剤;アルキルベンゼン、アルキルナフタ
レンなどの芳香族炭化水素系溶剤およびこれらの混合物
が挙げられる。これらの中では脂肪族炭化水素系溶剤で
沸点が150〜300℃ものが好ましく、沸点が180
〜260℃のものが更に好ましい。沸点が150℃未満
では臭気および引火危険性に問題が生じ、また沸点が3
00℃を越えると洗浄後の乾燥性が悪くなるので好まし
くない。(A)、(D)を併用する場合、本発明の洗浄
剤中の(A)の量は通常10重量%以上であり、炭化水
素系溶剤(D)の量は、(A)+(D)の合計量の通常
90重量%以下、好ましくは20〜80重量%である。
Further, the cleaning agent of the present invention may be a combination of (A) and a hydrocarbon solvent (D), and the range of stains can be widened by the combined use. Examples of the hydrocarbon solvent (D) include aliphatic hydrocarbon solvents such as normal paraffin, isoparaffin, cycloparaffin, kerosene and terpene; aromatic hydrocarbon solvents such as alkylbenzene and alkylnaphthalene, and a mixture thereof. Among these, aliphatic hydrocarbon solvents having a boiling point of 150 to 300 ° C. are preferable, and a boiling point of 180
Those having a temperature of up to 260 ° C are more preferable. If the boiling point is less than 150 ° C, there will be problems with odor and fire hazard, and the boiling point will be 3
When the temperature exceeds 00 ° C, the drying property after washing is deteriorated, which is not preferable. When (A) and (D) are used in combination, the amount of (A) in the detergent of the present invention is usually 10% by weight or more, and the amount of the hydrocarbon solvent (D) is (A) + (D 90% by weight or less, preferably 20 to 80% by weight, of the total amount of the above).

【0014】更に、本発明の洗浄剤中には、必要に応じ
て他の溶剤、シリコンなどの消泡剤、アミン系またはフ
ェノール系の酸化防止剤、防錆剤、防菌剤、防黴剤等が
配合できる。
Further, in the detergent of the present invention, if necessary, other solvent, antifoaming agent such as silicone, amine-based or phenol-based antioxidant, anticorrosive agent, antibacterial agent, antifungal agent. Etc. can be blended.

【0015】本発明の洗浄剤は浸漬洗浄法、超音波洗浄
法、噴流法、スプレー法、蒸気洗浄法等の各種の洗浄法
を適用して使用することができる。
The cleaning agent of the present invention can be used by applying various cleaning methods such as an immersion cleaning method, an ultrasonic cleaning method, a jet method, a spray method and a steam cleaning method.

【0016】[0016]

【実施例】以下実施例により本発明を更に説明するが、
本発明はこれに限定されるものではない。以下、実施例
中の部は重量部を示す。
The present invention will be further described with reference to the following examples.
The present invention is not limited to this. Hereinafter, parts in the examples are parts by weight.

【0017】実施例1〜6、比較例1,2 下記の表1に示す組成の洗浄剤をそれぞれ調整し、各洗
浄剤について次に示す洗浄力テストにより汚染物質除去
性を評価した。その結果を表1に示す。
Examples 1 to 6, Comparative Examples 1 and 2, detergents having the compositions shown in Table 1 below were prepared, and the detergent removal properties of the detergents were evaluated by the following detergency tests. The results are shown in Table 1.

【0018】(洗浄テスト1)研磨洗浄した金属鋼板に
汚染物質(鉱物油70%、植物油20%、オレイン酸1
0%)を塗布し、室温で24時間風乾して汚染板のテス
トピースを作成した。このテストピースをそれぞれの洗
浄剤中で超音波洗浄(50℃で1分間)した後、50℃
の熱風で乾燥させた。次いで、鋼板に残存している汚染
物質を四塩化炭素で抽出し、赤外吸収スペクトルで吸光
度を測定し、吸光度と汚染物質濃度との関係を示す検量
線から洗浄率を求めた。
(Cleaning test 1) Pollutants (mineral oil 70%, vegetable oil 20%, oleic acid 1
0%) was applied and air dried at room temperature for 24 hours to prepare a test piece of a contaminated plate. After ultrasonic cleaning (1 minute at 50 ° C) of each test piece in each cleaning agent, 50 ° C
It was dried with hot air. Then, the contaminants remaining on the steel sheet were extracted with carbon tetrachloride, the absorbance was measured by an infrared absorption spectrum, and the cleaning rate was obtained from a calibration curve showing the relationship between the absorbance and the contaminant concentration.

【0019】(洗浄テスト2)清浄なガラス板に市販の
ロジン系ハンダフラックス(千住金属(株)製フラック
スSR−12A−20)を塗布後、150℃で加熱乾燥
して汚染板のテストピースを作成した。このテストピー
スをそれぞれの洗浄剤中に浸漬(50℃で1分間)し、
さらに流水でリンス、乾燥してガラス板上に残存するフ
ラックスの量を次の基準で目視評価した。 ○:ガラス板上にフラックスなし △:ガラス板上にフラックス一部あり ×:ガラス板上にフラックス多い
(Cleaning test 2) A commercially available rosin-based solder flux (Flux SR-12A-20 manufactured by Senju Metal Co., Ltd.) was applied to a clean glass plate, and then heated and dried at 150 ° C. to give a test piece of a contaminated plate. Created. Immerse this test piece in each cleaning agent (1 minute at 50 ℃),
Further, the amount of flux remaining on the glass plate after being rinsed with running water and dried was visually evaluated according to the following criteria. ◯: No flux on the glass plate △: Some flux on the glass plate ×: A large amount of flux on the glass plate

【0020】(洗浄テスト3)250メッシュの紗張り
のポリエステル製スクリーン印刷版に市販のインク(ア
サヒ化研(株)製ソルダーレジストUVF−2G)を塗
布し、25℃で5分間風乾して汚染板のテストピースを
作成した。このテストピースを洗浄剤中で超音波洗浄
(40℃で1分間)した後、スクリーン印刷版に残存す
るインクの量を次の基準で目視評価した。 ◎:スクリーン印刷版上にインクなし ○:スクリーン印刷版上にインクが極わずかに残存 △:スクリーン印刷版上にインクが薄い膜状で残存 ×:スクリーン印刷版上にインクが多く残存
(Washing test 3) A commercially available ink (Solder resist UVF-2G manufactured by Asahi Kaken Co., Ltd.) was applied to a 250 mesh mesh screened polyester screen printing plate, and air-dried at 25 ° C. for 5 minutes to contaminate it. The test piece of the board was created. After ultrasonically cleaning this test piece in a cleaning agent (at 40 ° C. for 1 minute), the amount of ink remaining on the screen printing plate was visually evaluated according to the following criteria. ◎: No ink on the screen printing plate ○: Very little ink remained on the screen printing plate △: Ink remained as a thin film on the screen printing plate ×: Large amount of ink remained on the screen printing plate

【0021】(洗浄テスト4)洗浄前のステンレス伸線
(径:2mm;フッ素系滑剤が汚染物質として付着)の
テストピース(長さ60mm)6本を洗浄剤中で浸漬洗
浄(50℃で20分間)した後、60℃の熱風で乾燥さ
せた。次いで、黒色台紙上に6本の伸線を面状に密に並
べて固定し、光沢計(日本電色工業(株)製)で75゜
での反射率(%)を測定して洗浄の程度を評価した。数
値の大きい方が光沢が大きく、洗浄性が良好である。
(Washing test 4) Six test pieces (60 mm in length) of stainless wire drawing (diameter: 2 mm; fluorine-based lubricant adhered as a pollutant) before washing were immersed and washed in a detergent (20 at 50 ° C.). Then, it was dried with hot air at 60 ° C. Then, the 6 drawn wires were closely arranged in a plane on a black mount and fixed, and the degree of cleaning was measured by measuring the reflectance (%) at 75 ° with a gloss meter (manufactured by Nippon Denshoku Industries Co., Ltd.). Was evaluated. The larger the value, the greater the gloss and the better the washability.

【0022】[0022]

【表1】 [Table 1]

【0023】表1から明らかなように特定の化合物から
なる本発明の洗浄剤は、他の代替洗浄剤である炭化水素
系洗浄剤やアルコール系洗浄剤よりも幅広い洗浄力の点
で優れており、従来洗浄剤である1,1,1−トリクロ
ロエタンにほぼ匹敵する幅広い洗浄力を有している。ま
た、実施例6の本発明の洗浄剤は、引火点がなく消防法
上の非危険物に該当し、防火安全性の点でも優れてい
る。
As is clear from Table 1, the cleaning agent of the present invention composed of a specific compound is superior to other alternative cleaning agents such as hydrocarbon-based cleaning agents and alcohol-based cleaning agents in a wide range of cleaning power. It has a wide range of detergency almost equal to that of conventional 1,1,1-trichloroethane. Further, the cleaning agent of the present invention of Example 6 has no flash point, corresponds to a non-dangerous substance under the Fire Service Law, and is excellent in fire safety.

【0024】[0024]

【発明の効果】本発明の洗浄剤は、各種の汚れに対する
洗浄力が従来の塩素化炭化水素系溶剤と同等であり、オ
ゾン層破壊物質の1,1,1−トリクロロエタンの代替
洗浄剤として広範囲の産業分野で使用できる。
EFFECT OF THE INVENTION The cleaning agent of the present invention has a detergency against various stains equivalent to that of a conventional chlorinated hydrocarbon solvent, and is widely used as an alternative cleaning agent for 1,1,1-trichloroethane which is an ozone depleting substance. It can be used in the industrial field.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 炭素数2〜6の脂肪族アルデヒド1種以
上3分子が重合してなるグリコールモノエステル化合物
もしくはそのエーテル化ないしエステル化物(A)1種
以上からなることを特徴とする洗浄剤。
1. A detergent comprising a glycol monoester compound obtained by polymerizing one or more 3 molecules of an aliphatic aldehyde having 2 to 6 carbon atoms or one or more etherification or esterification products (A) thereof. .
【請求項2】 (A)を10重量%以上含有し、更にグ
リコールエーテル系化合物(B)を90%重量以下含有
してもよい請求項1記載の洗浄剤。
2. The cleaning agent according to claim 1, which may contain 10% by weight or more of (A) and 90% by weight or less of glycol ether compound (B).
【請求項3】 (A)を10重量%以上含有し、更に水
50重量%以下および必要により界面活性剤(C)を2
0重量%以下含有してもよい請求項1または2記載の洗
浄剤。
3. A content of 10% by weight or more of (A), 50% by weight or less of water, and optionally 2% of a surfactant (C).
The cleaning agent according to claim 1 or 2, which may be contained in an amount of 0% by weight or less.
【請求項4】 該脂肪族アルデヒドがアセトアルデヒ
ド、プロピルアルデヒド、n−ブチルアルデヒドまたは
イソブチルアルデヒドである請求項1〜3の何れかに記
載の洗浄剤。
4. The cleaning agent according to claim 1, wherein the aliphatic aldehyde is acetaldehyde, propyl aldehyde, n-butyraldehyde or isobutyraldehyde.
【請求項5】 (A)を10重量%以上含有し、更に炭
化水素系溶剤(D)を(A)、(D)合計量に対し90
重量%以下含有してもよい請求項1記載の洗浄剤。
5. The composition contains 10% by weight or more of (A), and further contains 90% by weight of a hydrocarbon solvent (D) with respect to the total amount of (A) and (D).
The cleaning agent according to claim 1, which may be contained in an amount of not more than 5% by weight.
【請求項6】 金属加工品、電子部品、光学部品、樹脂
成形品もしくは印刷版用の洗浄剤である請求項1〜5の
何れかに記載の洗浄剤。
6. The cleaning agent according to claim 1, which is a cleaning agent for metal working products, electronic parts, optical parts, resin molded products or printing plates.
JP31256493A 1993-11-17 1993-11-17 Detergent Pending JPH07138595A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31256493A JPH07138595A (en) 1993-11-17 1993-11-17 Detergent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31256493A JPH07138595A (en) 1993-11-17 1993-11-17 Detergent

Publications (1)

Publication Number Publication Date
JPH07138595A true JPH07138595A (en) 1995-05-30

Family

ID=18030736

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31256493A Pending JPH07138595A (en) 1993-11-17 1993-11-17 Detergent

Country Status (1)

Country Link
JP (1) JPH07138595A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019196425A (en) * 2018-05-08 2019-11-14 日本化薬株式会社 Clear ink

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019196425A (en) * 2018-05-08 2019-11-14 日本化薬株式会社 Clear ink

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