JPH06279788A - Water-soluble resin solution composition - Google Patents

Water-soluble resin solution composition

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Publication number
JPH06279788A
JPH06279788A JP10582893A JP10582893A JPH06279788A JP H06279788 A JPH06279788 A JP H06279788A JP 10582893 A JP10582893 A JP 10582893A JP 10582893 A JP10582893 A JP 10582893A JP H06279788 A JPH06279788 A JP H06279788A
Authority
JP
Japan
Prior art keywords
pyrrolidone
water
composition
solvent
isoprene
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
JP10582893A
Other languages
Japanese (ja)
Inventor
Ikue Kouno
伊久枝 河野
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.)
RAKU KK
Raku KK
Original Assignee
RAKU KK
Raku KK
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 RAKU KK, Raku KK filed Critical RAKU KK
Priority to JP10582893A priority Critical patent/JPH06279788A/en
Publication of JPH06279788A publication Critical patent/JPH06279788A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain the composition which is safe and has an excellent effect of dissolving and removing contaminants by using a pyrrolidone-base organic solvent and a specified isoprene-skeleton-containing terpene compound as the essential components. CONSTITUTION:The composition is produced by mixing a pyrrolidone-base organic solvent (e.g. N-methyl-pyrrolidone) and a terpene compound, including 10C monoterpene to 15C sesquiterpene, consisting of isoprene skeletons as the smallest units as the essential components and further mixing the obtained mixture with optionally a hydrophilic surfactant (e.g. sorbitan fatty acid ester). Examples of the terpene compounds include d-limonene, l-limonene, alpha-pinene, myrcene and 2,6-dimethyloctane. This composition has an effect of speedily removing high-molecular resinous dirt, an oil stain of tar, etc., has no ignitability, causes no environmental pollution and is desirable for cleaning precision machines, etc.

Description

【発明の詳細な説明】Detailed Description of the Invention

〔0001〕 〔産業上の利用分野〕本発明は鉱物油.高分子樹脂物
質.タール系物質.油性埃塵混合物.化石煤煙物質.金
属酸化物含有.有機高分子物などの汚染物質を安全に適
格にしかも後処理を簡便に問題を有しないように処理す
るのに適した水溶性樹脂溶解組成物に関するもので具体
的にはピロリドン系有機溶剤とある種のテルペン化合物
とを必須成分とした組成物を特定した水溶性樹脂溶解組
成物に関するものである。従来からこの種の汚染物洗浄
剤としては大別して次の2つの系統のものが常用されて
きた。それに代わって天然植物系の抽出物としてテルペ
ン系化合物を安全上の有利性から利用したものも大いに
注目され上市されている。1つは有機塩素系溶剤(例え
ばトリクロルエタン.テトラクロールエチレントリクロ
ルエチレン.又は弗素含有のフルオルハロゲン化炭化水
素俗にフッ素系ソルベントというもの。今1つはトルエ
ン.キシレン.ヘキサン.アセトン.パラフィン.ケロ
シン.など石油系引火性炭化水素であるが両者共環境上
又は健康上あるいは危険物.劇毒物など取締対象物とし
て社会上の大きな制約〔従来の技術〕をうけつつある。
テルペン系のリモネンを含む油性洗浄剤としては例えば
特開第3−6300に開示された非イオン界面活性剤と
の併用がある。あるいは市販品でオレンジ系のソルベン
トを含む水溶性クリーナーと称されるものはD−リモネ
ンを界面活性剤で可溶化して洗浄剤として供しようとい
うものである。一方では水溶性有機溶剤が比較的多く利
用される。例えば酢酸エステル.ジメチルホルムアミ
ド.ジメチルスルホキシド.ジアセトンアルコール.ベ
ンジルアルコール.ジオキサン.テトラヒドロフラン.
アセトニルアセトン.酪酸エステルなどがあげられるが
芳香臭が強く又分散し難くLD50などの毒性も大きく
不安な要素を多く有している。それだけでなく洗浄力の
スピード.溶解能.などはかなり制約されるものであ
る。 〔0002〕 〔発明が解決しようとする課題〕本発明はこのような従
来の洗浄剤を調査し種々の問題点を安全に確実に解決す
ることに成功したものである。即ち従来の問題点は (1)有機ハロゲン系物質に代表される不燃性ソルベン
トは絶対的に地下水汚染.人の健康への重大なる障害発
生.大気オゾンの破壊.二次処理の困難性など。 (2)可燃性の石油系ソルベントは水溶性なきものが多
く生分解し難いこと。引火性が高く消防法の制約.ある
いは方向族系(例 キシロール.トルオールなど)は劇
毒物.犯罪への招来を起こすもの更には溶解力(洗浄
力)が不充分であり第一目的(クリーナー)に不満が残
ることなど。 (3)水溶性有機溶剤も又親水性の故に樹脂や油類の溶
解力に乏しく.スピード能率も不充分で実用的見地から
完全代用にはなりえないことに加えて汚染物が転移する
ことによって二次汚染.二次災害を惹起させる懸念もあ
る。 (4)一方イソプレン系のテルペンソルベントは芳香性
が強く残香現象が長びいてかえって作業環境を悪化させ
る。更に溶解力は鉱物油や液状の低分子汚染物質にはあ
る程度有効なるも樹脂に代表される高分子(MWが1万
以上)系のものには著しく劣ることが否めないこと及び
非水性のために界面活性剤との併用によっても界面活性
剤は樹脂溶解に積極的に機能しないか明らかである。 〔0003〕 〔課題を解決するための手段〕本発明は従来のこの称な
る種々の問題点に注目し次の2種の水性.非水性の洗剤
を併用しこの解決をみることが出来たものである。即ち
ピロリドン系有機溶剤とイソプレン骨格(C)を
最少単位とした炭素数10のモノテルペンから炭素数1
5のセスキテルペンとを必須成分とした混合溶剤から基
本的になる組成物が最適であることを見い出したもので
ある。必要によって界面活性剤を併用することである。
ピロリドン系溶剤としてはN−メチル−2ピロリドン.
2−ピロリドン.3−ピロリドンなどの異環芳香族溶剤
である。当該溶剤は強力な樹脂溶解力.油脂溶解力.が
あることは周知の事実であり本発明者も先願(特願平−
4−42464)で記述したとおりであるが極性が大な
る為水との吸着性(吸湿性)に富に安定性や金属部分へ
の影響.非水性作業工程での残湿性及びアフター処理の
再汚染防止作用及び独特の異臭(アミン系)が有するの
で不快感があるなどの問題をもたらすことがある。この
為に香料の併用.植物鉱物系の油剤.腐食防止剤の併
用.なども考えられるがかえってピロリドン系溶剤の溶
解特性を損ない又混合系の経日安定性化学変化のおそれ
が懸念される。一方テルペン系溶剤は耐水性の芳香臭の
強いしかもポリマー系汚れ(樹脂.ベヒクル.フイルム
状形成物.タール.ピッチ)の溶解力に劣って欠点があ
る。ところがこれらピロリドン系溶剤とテルペン系溶剤
を併用することによりそれぞれの有する欠点が旨く緩和
されおどろく程の諸効果が本発明の要旨である。テルペ
ン系溶剤はイソプレン骨格(C)を単位となし炭
素数がC10〜C15のモノ〜セスキ テルペンがあげ
られ代表的なものはD−リモネン.l−リモネン.α−
ピネン.β−ピネン.Pメンタン.ミルセン.2,6ジ
メチルオクタン.カンファンなどがあげられる。これか
ら強烈な芳香臭を有し植物精油として香料の外天然系
(植物系)溶剤(ソルベント)として使用されてきた
(塗料.ペイント.インキ.絵の具建材補助剤など)最
も代表的な組み合わせは で必要によって界面活性剤又は水分あるいは他の有機溶
剤(例えば疎水性では炭化水素系.親水性ではグリコー
ル系 アミン系.ケトン系.アルコール系)が加わる 界面活性剤は洗浄剤として使用するときは再汚染防止.
乳化目的として重要な物質である。例えばポリオキシエ
チレンアルキルエーテル.ポリオキシエチレンアルキル
アミン.ポリオキシエチレンポリオキシプロピレンエー
テルなどのノニオン,脂肪酸塩.アルキルベンゼンスル
ホン酸塩.アルキル硫酸塩.アルキルリン酸塩.アルキ
ルスルホン酸塩.アルキルナフタレンスルホン酸塩.な
どのアニオン,第4級アンモニューム.脂肪酸アミン.
などのカチオン,ベタイン.イミダゾリン.などの両性
のものが上げられる。 〔0004〕 〔作 用〕本発明は親水性のピロリドン系溶剤と疎水
性のテルペン系溶剤を組み合わせた混合溶剤系が樹脂洗
浄溶解力.再汚染防止作用.作業性(快適性.スピード
アップ)が改善される他 水系での処理が可能となって
大気.水質.土壌などへの各種溶剤の汚染.水分を混合
することもでき危険物の適用も大巾に緩和することがで
きるなどのすぐれた結果をもたらすこととなる 利用分野は電子部材の洗浄(IC.LSI.コンデンサ
ー.バッテリー.液晶)ペイント.インキ.各種ベヒク
ル.ワニス.ラテックスなどの溶解及びそのリムーバー
重質な(植物油.鉱物油)油汚れのスピード除去.ドラ
イクリーニング剤.精密機械(ファインメカニカル)の
洗浄.金型洗浄.化粧品のエナメル,ラッカー,顔料,
レーキ,農薬などの溶解分散ガラス,レンズ,貴金属な
どの宝飾部品の洗浄に巾広く安全に能率よく使用でき
る。加えてピロリドン系の溶剤の高価な面がテルペン系
溶材の併用で有利なコストとなり代替溶剤の経済的負担
軽減にも有利に働き安心して広く利用することができ
る。同時に人間を含む生物への影響力が少なく水質.大
気など環境へも少ない以下代表的な実施例をあげて具体
的に説明する。 〔0005〕 〔実 施 例〕以下の配合からなる樹脂溶解組成物を試
作して以下のテストを行った。 〔0006〕
[0001] [Industrial field of application] The present invention relates to a mineral oil. Polymer resin material. Tar-based substance. Oily dust mixture. Fossil soot material. Contains metal oxide. It relates to a water-soluble resin-dissolved composition suitable for safely and qualitatively treating pollutants such as organic macromolecules and easily performing post-treatment without causing a problem. Specifically, it is a pyrrolidone-based organic solvent. The present invention relates to a water-soluble resin-dissolved composition in which a composition containing one kind of terpene compound as an essential component is specified. Conventionally, as a contaminant cleaning agent of this type, the following two systems have been commonly used. Instead, a terpene-based compound that is used as a natural plant-based extract from the viewpoint of safety is also receiving much attention and put on the market. One is an organic chlorine solvent (for example, trichloroethane.tetrachlorethylenetrichloroethylene.) Or a fluorine-containing fluorohalogenated hydrocarbon, commonly called a fluorine solvent. The other is toluene.xylene.hexane.acetone.paraffin. Although they are petroleum-based flammable hydrocarbons such as kerosene, both are subject to major social restrictions [prior art] as environmental, health, or dangerous substances.
As an oil-based detergent containing terpene-based limonene, for example, there is a combined use with a nonionic surfactant disclosed in JP-A-3-6300. Alternatively, what is called a water-soluble cleaner containing an orange solvent which is a commercial product is one in which D-limonene is solubilized with a surfactant and used as a cleaning agent. On the other hand, water-soluble organic solvents are used relatively often. For example, acetate ester. Dimethylformamide. Dimethyl sulfoxide. Diacetone alcohol. benzyl alcohol. Dioxane. Tetrahydrofuran.
Acetonylacetone. Examples thereof include butyric acid ester, but they have a strong aromatic odor, are difficult to disperse, and have large toxicity such as LD 50 and have many uneasy factors. Not only that, but the speed of detergency. Solubility. Etc. are quite limited. [Problems to be Solved by the Invention] The present invention has succeeded in investigating such conventional cleaning agents and safely and surely solving various problems. In other words, the conventional problems are: (1) Nonflammable solvents represented by organic halogen-based substances are absolutely contaminated with groundwater. Occurrence of serious damage to human health. Destruction of atmospheric ozone. Difficulty in secondary processing, etc. (2) Most flammable petroleum-based solvents are not water-soluble and are difficult to biodegrade. It is highly flammable and is a restriction of the Fire Service Act. Or direction group system (eg xylol, toluol, etc.) is a poisonous substance. What causes a crime, and further, the dissolving power (cleansing power) is insufficient and the first purpose (cleaner) remains unsatisfied. (3) Since the water-soluble organic solvent is also hydrophilic, it has a poor ability to dissolve resins and oils. In addition to the fact that it cannot be a complete substitute from a practical point of view due to insufficient speed efficiency, secondary pollution occurs due to the transfer of contaminants. There is also a concern that it may cause a secondary disaster. (4) On the other hand, the isoprene-based terpene solvent has a strong aromaticity and a long residual scent phenomenon, which rather deteriorates the working environment. Furthermore, its dissolving power is effective to some extent for mineral oil and liquid low-molecular pollutants, but it is undeniably inferior to that of polymers (MW of 10,000 or more) represented by resins. It is clear that the surfactant does not function positively in dissolving the resin even when used in combination with the surfactant. [0003] [Means for Solving the Problems] In the present invention, attention is paid to these various conventional problems, and the following two types of aqueous solutions are used. I was able to see this solution by using a non-aqueous detergent together. That is, a pyrrolidone-based organic solvent and an isoprene skeleton (C 5 H 8 ) are used as a minimum unit to obtain a C 1 to C 1 monoterpene.
It has been found that a composition basically consisting of a mixed solvent containing the sesquiterpene of 5 as an essential component is optimum. It is to use a surfactant together if necessary.
As the pyrrolidone-based solvent, N-methyl-2pyrrolidone.
2-pyrrolidone. Heterocyclic aromatic solvents such as 3-pyrrolidone. The solvent has a strong resin dissolving power. Oil and fat dissolving power. It is a well-known fact that the present inventor also applied for a prior application (Japanese Patent Application No.
As described in 4-42464), since it has a large polarity, it is highly adsorbable with water (hygroscopicity) and has stability and effects on metal parts. This may cause problems such as residual moisture in a non-aqueous work process, anti-redeposition action of after-treatment and a unique off-odor (amine type), which causes discomfort. For this purpose, a fragrance is used together. Oil based on plant minerals. Combined use of corrosion inhibitors. However, there is concern that the dissolution characteristics of the pyrrolidone-based solvent may be impaired and that the chemical stability of the mixed system may change over time. On the other hand, the terpene-based solvent has a drawback that it is inferior in water-solubility, has a strong aromatic odor, and is inferior in dissolving power of polymer-based stains (resin. Vehicle. Film-shaped product. Tar. Pitch). However, by using the pyrrolidone-based solvent and the terpene-based solvent in combination, the drawbacks of each of them are alleviated, and various effects that are surprising are the gist of the present invention. The terpene-based solvent is a mono-sesquiterpene having an isoprene skeleton (C 5 H 8 ) as a unit and having a carbon number of C 10 to C 15 , and a typical one is D-limonene. l-limonene. α-
Pinene. β-pinene. P Mentan. Milsen. 2,6 dimethyl octane. Can fan and so on. From now on, it has a strong aromatic odor and has been used as a plant essential oil as an external natural (plant) solvent (solvent) for perfumes (paint, paint, ink, paint building material auxiliary agent, etc.). If necessary, add surfactant or water or other organic solvent (eg hydrocarbon type for hydrophobic type, glycol type, amine type, ketone type, alcohol type for hydrophilic type). Prevention of pollution.
It is an important substance for the purpose of emulsification. For example, polyoxyethylene alkyl ether. Polyoxyethylene alkylamine. Nonionic and fatty acid salts such as polyoxyethylene polyoxypropylene ether. Alkylbenzene sulfonate. Alkyl sulfate. Alkyl phosphate. Alkyl sulfonate. Alkylnaphthalene sulfonate. Anions, etc., quaternary ammonium. Fatty acid amines.
Cations such as, betaine. Imidazoline. And so on. [Operation] In the present invention, a mixed solvent system in which a hydrophilic pyrrolidone-based solvent and a hydrophobic terpene-based solvent are combined has a resin cleaning solubility. Recontamination prevention action. Workability (comfort, speedup) is improved, and in addition to being able to be treated in a water-based atmosphere. Water quality. Contamination of various solvents to soil. It has excellent results in that it can mix water and can significantly reduce the application of dangerous substances. The field of application is cleaning of electronic parts (IC.LSI.condenser.battery.liquid crystal) paint. ink. Various vehicles. varnish. Dissolution of latex and its remover Speedy removal of heavy (vegetable oil, mineral oil) oil stains. Dry cleaning agent. Cleaning of precision machinery (fine mechanical). Mold cleaning. Cosmetic enamel, lacquer, pigment,
It can be widely and safely and efficiently used for cleaning rake, glass for dissolving and dispersing agricultural chemicals, lenses, jewelry parts such as precious metals. In addition, the expensive surface of the pyrrolidone-based solvent becomes advantageous cost when the terpene-based solvent is used in combination, which also contributes to reducing the economic burden of the alternative solvent and can be widely used with peace of mind. At the same time, the quality of water has little influence on living things including humans. Specific examples will be given below with reference to the following representative examples that are less environmentally friendly. [0005] [Practical example] A resin-dissolved composition having the following composition was manufactured as a trial and the following tests were conducted. [0006]

【表1】 〔0007〕[Table 1] [0007]

【表2】 の5×5cm プレート(2mm厚)に (a)カーボンブラックとクロロホルム及び流動パラフ
ィン 硅石粉末.卵黄油.モノオレインからなる汚垢を
cm当り1,5g塗布し1週間20°C下で放置する (b)ポリ塩化ビニール.リン酸トリクレジル.トリク
ロルエタン.カーボンブラックの溶液をcm 0,8
〜1,2g塗布し30°Cで30日間放置する 試作作品の組成物に(a).(b)の汚垢を塗布した金
属プレートを1分間浸漬し(500mlビーカー)引上
げて表面の状態を観察する。同時に各プレートを40°
C(60%RH〜70%RH)の恒温室に 〔0008〕
[Table 2] (A) Carbon black, chloroform and liquid paraffin silica powder on a 5 × 5 cm plate (2 mm thick). Egg yolk oil. Apply 1.5g of the stain containing monoolein per cm 2 and leave it at 20 ° C for 1 week. (B) Polyvinyl chloride. Tricresyl phosphate. Trichloroethane. The carbon black solution was added to cm 2 0.8
Apply 1-2g and leave at 30 ° C for 30 days . (A). The metal plate coated with the dirt of (b) is immersed for 1 minute (500 ml beaker) and pulled up to observe the surface condition. 40 ° at the same time for each plate
C (60% RH-70% RH) in a thermostatic chamber [0008]

【表3】 48hrs放置し表面の性質を観察する。−− 観察 , 同時に嗅覚状況を調査した −− 観察 更に汚染除去液のC.O.D.を測定した C,O,D.(過マンガン酸カリ法) ↓(10% 水溶液) 〔外観テスト〕 〔嗅覚テスト〕 〔C,O,D : 10% 水溶液 ppm〕 1. 88 2. 72 3. 34 .240 .286 .188 .122 (テスト−2) 急性毒性 〔LD50 (Mouse)〕 1.5860 経口 mg/kg 2.7200 3.6760 .5800 .4160 .6120 .6770[Table 3] Let stand for 48 hours and observe the surface properties. --- Observation, and at the same time, the olfactory condition was investigated --- Observation Further, C. O. D. C, O, D. (Potassium permanganate method) ↓ (10% aqueous solution) [Appearance test] [Smell test] [C, O, D: 10% aqueous solution ppm] 1. 88 2. 72 3. 34. 240. 286. 188. 122 (Test-2) Acute toxicity [LD 50 (Mouse)] 1.5860 Oral mg / kg 2.7200 3.6760. 5800. 4160. 6120. 6770

〔0009〕 〔発明の効果〕以上より本発明の併用の混合溶剤は洗浄
力.金属などの損傷度.水質汚染.生体安全性.作業適
性(嗅覚)のいずれも単独品よりすぐれた効果があり併
せてピロリドン系のコスト減(20〜60%)も図るこ
とができるので産業上の利用効果は甚大なものがある。
特にフロン.有機塩素系.ピロリドン.グリコールエー
テル.引火性炭化水素(BTX.パラフィン.ペンタ
ン.ヘキサンなど)に比して代替えを必至とされる電子
産業(半導体.IC.トランジスター.回路.LCD.
LCなど)精密産業(光学機械.NC工作機械.ロボッ
ト.ベアリング.マイクロギア)ドライクリーニング
業.農業.染顔料.防虫剤の非水系物質の乳化剤.エネ
ルギー素材の助財(ガソリン・ジーゼル・その他)及び
家庭用の洗浄剤(天ぷら油.シミヌキ剤.グリース.エ
リアカ汚れ.変質油)などに安全に確実に快適に利用で
きる。
[0009] [Effect of the invention] As described above, the mixed solvent of the present invention has a detergency. Degree of damage to metal, etc. Water pollution. Biosafety. The workability (smell) is superior to that of a single product, and the cost of the pyrrolidone system can be reduced (20 to 60%). Therefore, the industrial application effect is great.
Especially CFC. Organic chlorine system. Pyrrolidone. Glycol ether. Compared to flammable hydrocarbons (BTX, paraffin, pentane, hexane, etc.), the electronic industry (semiconductor, IC, transistor, circuit, LCD.
Precision industries (optical machines, NC machine tools, robots, bearings, micro gears) Dry cleaning industry. Agriculture. Dye / pigment. Emulsifier of non-aqueous substance of insect repellent. It can be used safely, reliably and comfortably as an auxiliary material for energy materials (gasoline, diesel, etc.) and household cleaners (tempura oil, shiminuki agent, grease, area stain, altered oil), etc.

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Claims (2)

【特許請求の範囲】[Claims] 〔請求項 1〕 ピロリドン系有機洗剤とイソプレン骨
格(C)を最少単位として構成される炭素数10
のモノテルペンから炭素数15のセスキテルペンとを必
須成分とすることを特徴とする水溶性樹脂溶解組成物
[Claim 1] A carbon number 10 comprising a pyrrolidone-based organic detergent and an isoprene skeleton (C 5 H 8 ) as a minimum unit.
A water-soluble resin-dissolving composition, characterized in that the monoterpene of 1 to sesquiterpene having 15 carbon atoms is an essential component
〔請求項 2〕 ピロリドン系有機洗剤とイソプレン骨
格(C)を最少単位として構成される炭素数10
のモノテルペンから炭素数15のセスキテルペンとを必
須成分としてこれに親水性界面活性剤を含有する第一項
記載の水溶性樹脂溶解組成物。
[Claim 2] A pyrrolidone-based organic detergent and an isoprene skeleton (C 5 H 8 ) having 10 carbon atoms as a minimum unit.
2. The water-soluble resin-dissolving composition according to the first item, wherein the monoterpene to sesquiterpene having 15 carbon atoms is contained as an essential component and a hydrophilic surfactant is contained therein.
JP10582893A 1993-03-29 1993-03-29 Water-soluble resin solution composition Pending JPH06279788A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10582893A JPH06279788A (en) 1993-03-29 1993-03-29 Water-soluble resin solution composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10582893A JPH06279788A (en) 1993-03-29 1993-03-29 Water-soluble resin solution composition

Publications (1)

Publication Number Publication Date
JPH06279788A true JPH06279788A (en) 1994-10-04

Family

ID=14417921

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10582893A Pending JPH06279788A (en) 1993-03-29 1993-03-29 Water-soluble resin solution composition

Country Status (1)

Country Link
JP (1) JPH06279788A (en)

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