JPH05311200A - Alkaline detergent - Google Patents
Alkaline detergentInfo
- Publication number
- JPH05311200A JPH05311200A JP14813092A JP14813092A JPH05311200A JP H05311200 A JPH05311200 A JP H05311200A JP 14813092 A JP14813092 A JP 14813092A JP 14813092 A JP14813092 A JP 14813092A JP H05311200 A JPH05311200 A JP H05311200A
- Authority
- JP
- Japan
- Prior art keywords
- alkaline
- carbon atoms
- agent
- detergent
- average
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/06—Hydroxides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/16—Sulfonic acids or sulfuric acid esters; Salts thereof derived from divalent or polyvalent alcohols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、洗浄剤に関する。更に
詳しくは、油汚れなどに対する洗浄力が高く、界面活性
剤を安定に含有するアルカリ性洗浄剤に関する。FIELD OF THE INVENTION The present invention relates to detergents. More specifically, it relates to an alkaline detergent which has a high detergency against oil stains and the like, and which contains a surfactant in a stable manner.
【0002】[0002]
【従来の技術】従来、アルカリ性洗浄剤としては、ア
ルカリ水溶液に溶けない界面活性剤を可溶化剤を用いて
予め配合し1液化したもの(例えば、特開平1−301
799号公報)、アルカリ剤と界面活性剤を使用の際
に混合して用いるもの(例えば、特公平2−55799
号公報)等が知られている。2. Description of the Related Art Conventionally, as an alkaline cleaning agent, a surfactant which is insoluble in an alkaline aqueous solution is preliminarily blended with a solubilizing agent so as to be one liquid (for example, JP-A-1-301).
799), a mixture of an alkali agent and a surfactant when used (for example, Japanese Patent Publication No. 2-55799).
No. gazette) is known.
【0003】[0003]
【発明が解決しようとする課題】しかし、上記のもの
は、保管中の安定性が不十分であり、の組成物は、使
用する度混合しなければならない為作業性が悪いという
問題がある。However, the above-mentioned compositions have insufficient stability during storage, and the composition of (1) has a problem of poor workability because they must be mixed each time they are used.
【0004】[0004]
【課題を解決するための手段】本発明者は、これらの問
題を解決し、且つ従来と同等以上の洗浄力を有するアル
カリ性洗浄剤を得るべく鋭意検討した結果、アルカリ剤
と界面活性剤を安定に含有する1液性組成物とすること
ができ、且つこの組成物は洗浄力も高いことを見い出し
本発明に到達した。Means for Solving the Problems The present inventor has made diligent studies in order to solve these problems and obtain an alkaline detergent having a detergency equal to or higher than that of the conventional one. As a result, the alkaline agent and the surfactant are stabilized. It was found that the composition can be a one-component composition containing the above-mentioned composition, and that this composition also has a high detergency, and reached the present invention.
【0005】即ち、本発明は、下記一般式(1)で示さ
れる化合物(A−1)および/または下記一般式(2)
で示される化合物(A−2)から選ばれる界面活性剤
(A)およびアルカリ剤(B)を含有する水溶液により
構成されることを特徴とするアルカリ性洗浄剤である。 RO(R’O)xCH2CH(OH)CH2SO3M (1) (各式中、Rは直鎖又は分岐鎖の炭素数6 〜20のア
ルキル基、直鎖又は分岐鎖の炭素数6 〜20のアルケ
ニル基、直鎖又は分岐鎖の炭素数4〜12のアルキル基
をもつアルキルフェニル基;(R’O)xは炭素数2〜
4のアルキレンオキシドが平均Xモル付加していること
を示す;Mは水素、もしくは塩基;Xは0〜20;m、
nはいずれも1または2;m+n=3)That is, the present invention provides a compound (A-1) represented by the following general formula (1) and / or a general formula (2) below.
An alkaline detergent comprising an aqueous solution containing a surfactant (A) selected from the compound (A-2) represented by and an alkaline agent (B). RO (R'O) x CH 2 CH (OH) CH 2 SO 3 M (1) (In each formula, R is a linear or branched alkyl group having 6 to 20 carbon atoms, a linear or branched alkenyl group having 6 to 20 carbon atoms, or a linear or branched alkyl group having 4 to 12 carbon atoms. An alkylphenyl group having a group; (R′O) x has 2 to 2 carbon atoms
4 shows that the alkylene oxide of 4 is added on average X moles; M is hydrogen or a base; X is 0 to 20; m,
n is either 1 or 2; m + n = 3)
【0006】一般式(1)および(2)におけるRの具
体例としては、n−ヘキシル、n−オクチル、n−デシ
ル、n−ドデシル、n−テトラデシル、n−ヘキサデシ
ル、n−オクタデシル等の直鎖アルキル基;2−エチル
ヘキシル、2−ヘキシルデシル、イソステアリル等の分
岐鎖アルキル基;オレイル、リノレイル等の直鎖又は分
岐鎖のアルケニル基;ブチルフェノール、オクチルフェ
ノール、ノニルフェノール等の直鎖又は分岐鎖の炭素数
4〜12のアルキル基をもつアルキルフェニル基等が挙
げられる。(R’O)は炭素数2〜4のアルキレンオキ
シドが平均Xモル付加していることを示し、アルキレン
オキシドの具体例としては、エチレンオキシド、プロピ
レンオキシド、ブチレンオキシド等が挙げられる。好ま
しくはエチレンオキシド、プロピレンオキシドである。
また、アルキレンオキシドは1種類、又は2種類以上
で、2種類以上付加する場合の付加形式はランダム付加
でもブロック付加でもよい。Xは平均付加モル数であ
り、通常0〜20、好ましくは2〜10である。Mは、
水素原子または塩基であり、ナトリウム、カリウム等の
アルカリ金属;カルシウム、マグネシウム等のアルカリ
土類金属;メチルアミン、エチルアミン、プロピルアミ
ン、エチレンジアミン、ジエチレントリアミン等の炭素
数1〜4の脂肪族アミン塩基;アンモニウム基;モノエ
タノールアミン、ジエタノールアミン、トリエタノール
アミン等のアルカノールアミン塩基等が挙げられる。こ
れらのうち好ましいものは、ナトリウムおよびカリウム
である。mおよびnは1または2である。好ましくは、
mは1で、nは2である。Specific examples of R in the general formulas (1) and (2) include direct groups such as n-hexyl, n-octyl, n-decyl, n-dodecyl, n-tetradecyl, n-hexadecyl and n-octadecyl. Chain alkyl group; 2-ethylhexyl, 2-hexyldecyl, isostearyl, and other branched-chain alkyl groups; oleyl, linoleyl, and other straight-chain or branched-chain alkenyl groups; butylphenol, octylphenol, nonylphenol, and other straight-chain or branched-chain carbon groups Examples thereof include an alkylphenyl group having an alkyl group of 4 to 12. (R′O) means that an alkylene oxide having 2 to 4 carbon atoms is added in an average X moles, and specific examples of the alkylene oxide include ethylene oxide, propylene oxide, butylene oxide and the like. Ethylene oxide and propylene oxide are preferred.
The alkylene oxide may be one type or two or more types, and when two or more types are added, the addition form may be random addition or block addition. X is the average number of moles added, and is usually 0 to 20, preferably 2 to 10. M is
A hydrogen atom or a base, an alkali metal such as sodium and potassium; an alkaline earth metal such as calcium and magnesium; an aliphatic amine base having 1 to 4 carbon atoms such as methylamine, ethylamine, propylamine, ethylenediamine, diethylenetriamine; ammonium. Group; alkanolamine bases such as monoethanolamine, diethanolamine, triethanolamine and the like. Of these, preferred is sodium and potassium. m and n are 1 or 2. Preferably,
m is 1 and n is 2.
【0007】(A−1)の製法としては、アルコール類
もしくはそのアルキレンオキシド付加物にエピクロルヒ
ドリンを反応させた後閉環させたグリシジルエーテルに
重亜硫酸塩を反応させる方法がある。また、アルコール
類もしくはそのアルキレンオキシド付加物にエピクロル
ヒドリンを反応させた後亜硫酸塩を反応させる方法もあ
る。(A−2)の製法としては、アルコール類もしくは
そのアルキレンオキシド付加物にエピクロルヒドリンを
反応させた後閉環させたグリシジルエーテルにリン酸を
反応させる方法がある。また、アルコール類もしくはそ
のアルキレンオキシド付加物にエピクロルヒドリンを反
応させた後閉環させたグリシジルエーテルにリン酸を反
応させた後中和する方法もある。As a method of producing (A-1), there is a method of reacting alcohols or alkylene oxide adducts thereof with epichlorohydrin and then reacting cyclized glycidyl ether with bisulfite. There is also a method of reacting alcohols or alkylene oxide adducts thereof with epichlorohydrin and then reacting with sulfite. As the production method of (A-2), there is a method of reacting alcohols or alkylene oxide adducts thereof with epichlorohydrin and then reacting cyclized glycidyl ether with phosphoric acid. There is also a method in which alcohols or alkylene oxide adducts thereof are reacted with epichlorohydrin, and then glycidyl ether which is ring-closed is reacted with phosphoric acid and then neutralized.
【0008】本発明におけるアルカリ剤(B)として
は、アルカリ金属水酸化物(水酸化ナトリウム、水酸化
カリウムなど)、珪酸類のアルカリ金属塩(オルソ珪酸
ナトリウム、メタ珪酸ナトリウムなど)、リン酸類の金
属塩(トリポリリン酸ナトリウム、メタリン酸ナトリウ
ムなど)、アミン類(エチレンジアミン、アルカノール
アミンなど)等が挙げられる。Examples of the alkaline agent (B) in the present invention include alkali metal hydroxides (sodium hydroxide, potassium hydroxide, etc.), alkali metal salts of silicic acids (sodium orthosilicate, sodium metasilicate, etc.), and phosphoric acids. Examples thereof include metal salts (sodium tripolyphosphate, sodium metaphosphate, etc.), amines (ethylenediamine, alkanolamine, etc.), and the like.
【0009】本発明の洗浄剤には必要により、消泡剤を
含有させることができる。消泡剤としては、洗浄剤用に
一般に用いられるものならばいずれのものでもよく、ポ
リアルキレングリコール系消泡剤〔例えば、三洋化成工
業(株)製、カラリンDF〕等が挙げられる。本発明の
洗浄剤には必要により、キレート剤を含有させることも
できる。キレート剤としては、エチレンジアミンテトラ
酢酸、グルコン酸、ポリアクリル酸、及びそれらの塩等
が挙げられる。これらのうち好ましいものは、エチレン
ジアミンテトラ酢酸、及びその塩である。本発明にはそ
の他ノニオン系界面活性剤〔例えば、三洋化成工業
(株)製、ノニポール100〕や他のアニオン系界面活
性剤〔例えば、三洋化成工業(株)製、サンデットAL
H〕を含有することもできる。本発明の洗浄剤を構成す
る各成分の量は目的に応じて調整すれば良いが、通常重
量割合は以下の通りである。界面活性剤(A−1)およ
び/また(A−2)の量は、通常0.01〜30%、好
ましくは、0.1〜10%、アルカリ剤(B)の量は、
通常0.1〜50%、好ましくは、1〜30%である。
残部はその他の任意成分及び水である。If desired, the detergent of the present invention may contain an antifoaming agent. As the defoaming agent, any defoaming agent that is generally used for detergents may be used, and examples thereof include polyalkylene glycol-based defoaming agents [for example, Sanyo Kasei Kogyo Co., Ltd., Karalin DF] and the like. If desired, the cleaning agent of the present invention may contain a chelating agent. Examples of the chelating agent include ethylenediaminetetraacetic acid, gluconic acid, polyacrylic acid, and salts thereof. Among these, preferred is ethylenediaminetetraacetic acid, and salts thereof. In the present invention, other nonionic surfactants [for example, Sanyo Chemical Industry Co., Ltd., Nonipol 100] and other anionic surfactants [for example, Sanyo Chemical Industry Co., Ltd., Sandet AL
H] may also be included. The amount of each component constituting the detergent of the present invention may be adjusted according to the purpose, but the weight ratio is usually as follows. The amount of the surfactant (A-1) and / or (A-2) is usually 0.01 to 30%, preferably 0.1 to 10%, and the amount of the alkaline agent (B) is
It is usually 0.1 to 50%, preferably 1 to 30%.
The balance is other optional ingredients and water.
【0010】本発明の界面活性剤(A−1)および/ま
たは(A−2)は、金属、ガラス、プラスチック、およ
びこれらの複合材料等の硬質表面洗浄剤、浸透剤、精錬
剤等のアルカリ性洗浄剤の他にも一般的な洗浄剤として
利用することもできる。The surfactants (A-1) and / or (A-2) of the present invention are alkaline agents such as hard surface cleaning agents such as metals, glass, plastics, and composite materials thereof, penetrants, refining agents and the like. Besides the cleaning agent, it can be used as a general cleaning agent.
【0011】本発明の洗浄剤の製法を例示すると、アル
カリ剤(B)の水溶液中に界面活性剤(A−1)および
/または(A−2)、および必要により上記に例示した
任意成分を投入し、混合することにより本発明の洗浄剤
が得られる。As an example of the method for producing the cleaning agent of the present invention, the surfactant (A-1) and / or (A-2) and, if necessary, the optional components exemplified above in an aqueous solution of the alkaline agent (B). The cleaning agent of the present invention is obtained by charging and mixing.
【0012】[0012]
【実施例】以下、実施例により本発明を更に詳しく説明
するが、本発明はこれに限定されるものではない。又以
下の説明において、部及び%は、それぞれ重量部及び重
量%を表す。下記表1に示した配合処方に基づき本発明
のアルカリ性洗浄剤を得た。次いで下記に示した試験方
法で洗浄剤組成物の外観及び洗浄力を評価した。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto. In the following description, parts and% represent parts by weight and% by weight, respectively. The alkaline cleaner of the present invention was obtained based on the formulation shown in Table 1 below. Then, the appearance and detergency of the detergent composition were evaluated by the test methods shown below.
【0013】[0013]
【表1】 [Table 1]
【0014】表1の配合処方中の活性剤の略称は下記化
合物を表す。 <実施例> 〔スルホン酸塩〕(A-1) (A-1)-1:RO(R'O)x=n-ト゛テ゛カノール残基、M=ナトリウム (A-1)-2:RO(R'O)x=n-ト゛テ゛カノールエチレンオキシト゛平均7モル付加物
残基、M=カリウム (A-1)-3:RO(R'O)x=2-ト゛テ゛カノールエチレンオキシト゛平均5モル付加物
残基、M=ナトリウム (A-1)-4:RO(R'O)x=n-テ゛カノールエチレンオキシト゛平均7モル/フ゜ロヒ゜レ
ンオキシト゛平均5モルランタ゛ム付加物残基、M=ナトリウム (A-1)-5:RO(R'O)x=ノニルフェノールエチレンオキシト゛平均9モル付加物残
基、M=ナトリウム 〔リン酸塩〕(A-2) (A-2)-1:RO(R'O)x=2-エチルヘキシルアルコール残基、m=1,n=2、M=ナ
トリウム (A-2)-2:RO(R'O)x=n-ト゛テ゛カノールエチレンオキシト゛平均7モル付加物
残基、m=1,n=2、M=カリウム (A-2)-3:RO(R'O)x=2-ト゛テ゛カノールエチレンオキシト゛平均5モル付加物
残基、m=1,n=2、M=ナトリウム (A-2)-4:RO(R'O)x=n-テ゛カノールエチレンオキシト゛平均7モル/フ゜ロヒ゜レ
ンオキシト゛平均5モルランタ゛ム付加物残基、m=1,n=2、M=ナトリウム (A-2)-5:RO(R'O)x=ノニルフェノールエチレンオキシト゛平均4モル付加物残
基、m=1,n=2、M=ナトリウム <比較例> (A')-1 :(ノニルフェニル)フェニルエーテルシ゛スルホン酸ナトリウム (A')-2 :ノニルフェノールエチレンオキシト゛平均9モル付加物The abbreviations of the active agents in the formulations shown in Table 1 represent the following compounds. <Example> [Sulfonate] (A-1) (A-1) -1: RO (R'O) x = n-decanol residue, M = sodium (A-1) -2: RO (R 'O) x = n-dodecanol ethylene oxide average 7 mol adduct residues, M = potassium (A-1) -3: RO (R'O) x = 2-decanol ethylene oxide average 5 mol adduct residues, M = sodium (A-1) -4: RO (R'O) x = n-decanol ethylene oxide average 7 moles / propylene oxide average 5 moles random adduct residue, M = sodium (A-1) -5: RO (R'O) x = nonylphenol ethylene oxide average 9 mol adduct residue, M = sodium [phosphate] (A-2) (A-2) -1: RO (R'O) x = 2-ethylhexyl Alcohol residue, m = 1, n = 2, M = sodium (A-2) -2: RO (R'O) x = n-decanol ethylene oxide average 7 mol adduct residue, m = 1, n = 2, M = potassium (A-2) -3: RO (R'O) x = 2- Dode mosquito Nord ethyleneoxy preparative Bu average 5 Le adduct residue, m = 1, n = 2 , M = sodium (A-2) -4: RO (R'O) x = n- des Cats Nord ethyleneoxy preparative Bu average 7 moles / propylene Ren'okishito Bu average 5 Moruranta Bu beam adduct Residue, m = 1, n = 2, M = sodium (A-2) -5: RO (R'O) x = nonylphenol ethylene oxide average 4 mol adduct residue, m = 1, n = 2, M = Sodium <Comparative Example> (A ')-1: (nonylphenyl) phenyl ether sodium disulfonate (A')-2: Nonylphenol ethylene oxide average 9 mol adduct
【0015】洗浄剤の外観の試験方法 表1に示した配合処方に基づき混合し10分間攪拌した
後、1時間放置後の外観を観察する。 ○:分離、沈澱せず ×:分離、沈澱あり 洗浄力試験方法 軟鋼板(70×20mm)にカーボンブラック 2部と
大豆油 100部の混合物 0.1gをはけで均一に塗布
し、175〜180℃で1時間焼き付けしたものを空冷
して油汚れが付着した試験片を作成した。表1に示した
アルカリ洗浄剤を10倍に希釈し洗浄溶液を作成した。
30℃の洗浄溶液中に試験片を30秒間浸漬後、20℃
の静止水中で10秒間水洗後乾燥させた。次に洗浄した
試験片にセロテープをはりつけて、剥離すると残存する
汚れはセロテープ側に移るのでこのセロテープを白紙に
はりつけ、反射率をAKA光電管比色計で測定し、洗浄
率を求めた。 洗浄率(%)=(RW−RS)/(RO−RS)× 1
00 RO:原白紙の反射率 RS:洗浄前試験片の反射率 RW:洗浄後試験片の反射率Method of Testing the Appearance of the Detergent The mixture was mixed according to the formulation shown in Table 1 and stirred for 10 minutes, and then the appearance after standing for 1 hour is observed. ◯: No separation or precipitation X: Separation or precipitation Detergency test method 0.1 g of a mixture of 2 parts of carbon black and 100 parts of soybean oil was evenly applied to a mild steel plate (70 × 20 mm) by a brush, and 175 to 175 What was baked at 180 ° C. for 1 hour was air-cooled to prepare a test piece with oil stains. The alkaline cleaning agent shown in Table 1 was diluted 10 times to prepare a cleaning solution.
After soaking the test piece in the washing solution at 30 ° C for 30 seconds,
Was washed with water in still water for 10 seconds and then dried. Next, a cellophane tape was attached to the washed test piece, and the remaining stains were transferred to the cellophane tape when peeled off. Therefore, this cellophane tape was attached to a white paper, and the reflectance was measured with an AKA phototube colorimeter to obtain the washing rate. Cleaning rate (%) = (RW−RS) / (RO−RS) × 1
00 RO: reflectance of original blank paper RS: reflectance of test piece before washing RW: reflectance of test piece after washing
【0016】[0016]
【発明の効果】本発明の組成物は、下記効果を奏する。 (1)安定性が良い。従来の1液性アルカリ洗浄剤は安
定性に問題があった。 (2)作業性が良い。従来の2液性アルカリ洗浄剤は使
用時混合する手間を要した。 (3)油汚れの汚れに対し、洗浄力が高い。 上記効果を奏することから、本発明の組成物はアルカリ
性洗浄剤として有用である。The composition of the present invention has the following effects. (1) Good stability. The conventional one-pack alkaline cleaner has a problem in stability. (2) Good workability. The conventional two-liquid alkaline cleaner required time and effort for mixing. (3) High cleaning power against oil stains. Because of the above effects, the composition of the present invention is useful as an alkaline cleaner.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C11D 7:14) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location C11D 7:14)
Claims (2)
1)および/または下記一般式(2)で示される化合物
(A−2)から選ばれる界面活性剤(A)およびアルカ
リ剤(B)を含有する水溶液により構成されることを特
徴とするアルカリ性洗浄剤。 RO(R’O)xCH2CH(OH)CH2SO3M (1) (各式中、Rは直鎖又は分岐鎖の炭素数6 〜20のア
ルキル基、直鎖又は分岐鎖の炭素数6 〜20のアルケ
ニル基、直鎖又は分岐鎖の炭素数4〜12のアルキル基
をもつアルキルフェニル基;(R’O)xは炭素数2〜
4のアルキレンオキシドが平均Xモル付加していること
を示す;Mは水素、もしくは塩基;Xは0〜20;m、
nはいずれも1または2;m+n=3)1. A compound represented by the following general formula (1) (A-
1) and / or an alkaline cleaning comprising an aqueous solution containing a surfactant (A) selected from a compound (A-2) represented by the following general formula (2) and an alkaline agent (B). Agent. RO (R'O) x CH 2 CH (OH) CH 2 SO 3 M (1) (In each formula, R is a linear or branched alkyl group having 6 to 20 carbon atoms, a linear or branched alkenyl group having 6 to 20 carbon atoms, or a linear or branched alkyl group having 4 to 12 carbon atoms. An alkylphenyl group having a group; (R′O) x has 2 to 2 carbon atoms
4 shows that alkylene oxide of 4 is added on average X moles; M is hydrogen or a base; X is 0 to 20; m,
n is either 1 or 2; m + n = 3)
の式中の平均付加モル数Xが2〜10である請求項1記
載のアルカリ性洗浄剤。2. General formula (1) and / or general formula (2)
The alkaline detergent according to claim 1, wherein the average added mole number X in the formula is 2 to 10.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14813092A JP3142636B2 (en) | 1992-05-13 | 1992-05-13 | Alkaline cleaning agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14813092A JP3142636B2 (en) | 1992-05-13 | 1992-05-13 | Alkaline cleaning agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05311200A true JPH05311200A (en) | 1993-11-22 |
JP3142636B2 JP3142636B2 (en) | 2001-03-07 |
Family
ID=15445934
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14813092A Expired - Fee Related JP3142636B2 (en) | 1992-05-13 | 1992-05-13 | Alkaline cleaning agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3142636B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997045186A1 (en) * | 1996-05-31 | 1997-12-04 | Witco Corporation | Novel aromatic and aliphatic sulfonates and properties and applications thereof |
WO1999047101A3 (en) * | 1998-03-18 | 1999-11-25 | Lxr Biotechnology Inc | Compositions containing lysophosphatidic acids which inhibit apoptosis and uses thereof |
CN107164109A (en) * | 2017-03-31 | 2017-09-15 | 吴江创源新材料科技有限公司 | Cleaning fluid and preparation method thereof and cleaning before a kind of sapphire wafer annealing |
-
1992
- 1992-05-13 JP JP14813092A patent/JP3142636B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997045186A1 (en) * | 1996-05-31 | 1997-12-04 | Witco Corporation | Novel aromatic and aliphatic sulfonates and properties and applications thereof |
US5919975A (en) * | 1996-05-31 | 1999-07-06 | Witco Corporation | Aromatic and aliphatic sulfonates and properties and applications thereof |
WO1999047101A3 (en) * | 1998-03-18 | 1999-11-25 | Lxr Biotechnology Inc | Compositions containing lysophosphatidic acids which inhibit apoptosis and uses thereof |
EP1069895A2 (en) * | 1998-03-18 | 2001-01-24 | Lxr Biotechnology Inc. | Compositions containing lysophosphatidic acids which inhibit apoptosis and uses thereof |
EP1069895A4 (en) * | 1998-03-18 | 2002-07-31 | Lxr Biotechnology Inc | Compositions containing lysophosphatidic acids which inhibit apoptosis and uses thereof |
CN107164109A (en) * | 2017-03-31 | 2017-09-15 | 吴江创源新材料科技有限公司 | Cleaning fluid and preparation method thereof and cleaning before a kind of sapphire wafer annealing |
Also Published As
Publication number | Publication date |
---|---|
JP3142636B2 (en) | 2001-03-07 |
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