JPS5874800A - Liquid alkali detergent - Google Patents

Liquid alkali detergent

Info

Publication number
JPS5874800A
JPS5874800A JP17364081A JP17364081A JPS5874800A JP S5874800 A JPS5874800 A JP S5874800A JP 17364081 A JP17364081 A JP 17364081A JP 17364081 A JP17364081 A JP 17364081A JP S5874800 A JPS5874800 A JP S5874800A
Authority
JP
Japan
Prior art keywords
sodium
gum
liquid
substances
alkaline
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
JP17364081A
Other languages
Japanese (ja)
Other versions
JPH0433840B2 (en
Inventor
武司 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.)
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 JP17364081A priority Critical patent/JPS5874800A/en
Publication of JPS5874800A publication Critical patent/JPS5874800A/en
Publication of JPH0433840B2 publication Critical patent/JPH0433840B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Detergent Compositions (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本実明快アルカリ洗浄剤、殊に安定性及び洗浄性等に優
れた液状洗浄剤に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a practical alkaline cleaning agent, particularly a liquid cleaning agent with excellent stability and cleaning properties.

今日、金属類、プラスチックス等へのン・ツキ、塗装な
どの準備作業として多量のアルカリ洗浄剤が消費されて
いる。これらのアルカリ洗浄剤は、一般にアルカリ金属
の水酸化物、アルカ1ノ金属の中性塩、キレート剤、各
種のビルダー及び界面活性剤などが配合されたものであ
−2て、今日使用される洗浄剤の中、′過半量はヒ゛ル
り゛−酸成分どに界面活性剤を被覆、含浸等の手段で配
合、乾燥させた粒状又は粉状のものである。
Today, large amounts of alkaline cleaning agents are consumed in preparatory work such as coating metals, plastics, etc., and painting. These alkaline cleaning agents are generally blended with alkali metal hydroxides, neutral salts of alkali metals, chelating agents, various builders, surfactants, etc., and are used today. The majority of detergents are in the form of granules or powders, which are prepared by coating or impregnating a hylic acid component with a surfactant and then drying it.

しかし粒状、粉末等の固形のものは、嵩高である以外に
、使用時の計量の厄介さや容器から取り出す際における
微粉末の飛散など、作業上及び労働衛生上の問題が多い
。これに反し液状のものは、計量が容易であり、かつパ
イプ輸送が可能である等、前者に優る利点を有する反面
、塩析効果の関係で界面活性剤が分離、析出しゃ上の難
点を有する。本発明は、液状アルカリ洗浄剤における以
上の問題を解決した新しい洗浄剤組成物に関する。
However, in addition to being bulky, solid products such as granules and powders have many operational and occupational health problems, such as the difficulty of measuring them during use and the scattering of fine powder when taking them out of containers. On the other hand, while liquids have advantages over the former, such as being easy to measure and can be transported through pipes, they also have the disadvantage that the surfactant may separate and precipitate due to the salting-out effect. . The present invention relates to a new detergent composition that solves the above problems in liquid alkaline detergents.

従来、アルカリ水溶液中に界面活性剤を安定に配合せん
がための試みとして、 ill  アニオン界面活性剤又は低級アルコール等の
非イオン界面活性剤に対するハイドロトロピー作用(H
ydqrotropic  action、溶解度増大
作用)を利用する方法。
Conventionally, in an attempt to stably incorporate a surfactant into an alkaline aqueous solution, the hydrotropic effect (H
ydqrotropic action, solubility increasing action).

(2)界面活性剤のHLB値を低下させる方法。(2) A method of lowering the HLB value of a surfactant.

及  び (3)  アルカリ洗浄剤を2剤(一方は液体、他方は
液体又は粉粒体)に分割する方法。
and (3) a method of dividing the alkaline cleaning agent into two parts (one liquid and the other liquid or powder).

などが知ら、れている。etc. are known.

しかし、(1)のハイドロトロピー作用を利用する方法
では、性能の低下及び、殊にアニオン界面活性剤が添加
された場合には、それによる発泡性の増大が問題となっ
て来る。また(2)のHLBを低下させる方法によると
、洗浄性能が犠牲となる。さらに(3)の分割法は、作
業性の上で大きな不利をもたらす。このように、公知の
界面活性剤の析出防止手段はいづれも効果において不満
足であって、このことが液状洗浄剤の発展を妨ける原因
となっていた。
However, in the method (1) that utilizes hydrotropy, problems arise such as a decrease in performance and, especially when an anionic surfactant is added, a resulting increase in foaming properties. Further, according to the method (2) of lowering the HLB, cleaning performance is sacrificed. Furthermore, the division method (3) has a major disadvantage in terms of workability. As described above, all of the known means for preventing precipitation of surfactants are unsatisfactory in their effectiveness, which has hindered the development of liquid detergents.

しかるに、本発明者は液状アルカリ洗浄剤における沈澱
現象を防止する手段につき組織的な研究を試みた結果、
今般、多くの水溶性高分子物質が目的上極めて有用であ
ることを見出した。
However, as a result of conducting systematic research on means for preventing the precipitation phenomenon in liquid alkaline cleaning agents, the present inventor found that
It has now been discovered that a number of water-soluble polymeric substances are extremely useful for this purpose.

因みに、水溶性高分子物質は概ね親水性コロイド物質で
あって、これらコロイド物質の存在が難溶性物質の析出
乃至沈澱防止に奏効することば周知のことであるが、本
発明の対象である強いアルカリ性雰囲気において、しか
も多量の電解質の存在で強力な析出防止作用を奏するで
あることは簡単に予測できないことであって、本発明者
により始めて見出された新知見である。ともあれ、本発
明にいう親水性高分子物質とは例えば次のような物質を
いう。
Incidentally, water-soluble polymeric substances are generally hydrophilic colloidal substances, and it is well known that the presence of these colloidal substances is effective in preventing precipitation of poorly soluble substances. The fact that a strong precipitation prevention effect can be achieved in an atmosphere and in the presence of a large amount of electrolyte cannot be easily predicted, and is a new finding discovered for the first time by the present inventor. In any case, the hydrophilic polymer substances referred to in the present invention include, for example, the following substances.

(1)デ/プン類:バレイショデンプン、サツマイモデ
ンプン、タピオカデンプン、コムギデンプン、トウモロ
コシデンプン等。
(1) Starches: potato starch, sweet potato starch, tapioca starch, wheat starch, corn starch, etc.

(Jil  マンナン類:コンニャクマンナン等。(Jil Mannans: Konjac mannan, etc.

(―)  海藻粘液質二フノリ、寒天、ファーセラン、
カラギーナン等。
(-) Seaweed mucilage Nifunori, agar, farcelan,
Carrageenan et al.

(1■)  植物粘質物:トロロアオイ粘液、ヤマイモ
粘液、トラガントガム、アラビアガム、ガラヤガム、ア
ーモンドガム、アラビノガラクタン←苺→、ガラティガ
ム、ローカストビーンガム、タマリンドガム、タラガム
、クインンードガム、ペクチン、デキストリン等。
(1■) Plant mucilages: trumpet mucus, yam mucilage, tragacanth gum, arabic gum, galaya gum, almond gum, arabinogalactan←strawberry→, galati gum, locust bean gum, tamarind gum, tara gum, quince gum, pectin, dextrin, etc.

(v)  微生物粘質物:キサンタンガム、カードラン
、サクシノグルカン、プルラン、デキストラン、レバン
等。
(v) Microbial mucilages: xanthan gum, curdlan, succinoglucan, pullulan, dextran, levan, etc.

(VD  蛋白質:膠、ゼラチン、カゼイン、血漿蛋白
、ホエイ蛋白、ダイズ蛋白、コムギ蛋白、コラーゲン。
(VD Protein: glue, gelatin, casein, plasma protein, whey protein, soy protein, wheat protein, collagen.

(dD  セルロース及ヒ半合成セルロース詞導体:微
結晶セルロース、ビスコース、メチルセルロース(MC
)、エチルセルロース(EC)、ヒドロキシエチルセル
ロース(HEC)、カルボキシメチルセルロース(CM
C)。
(dD Cellulose and semi-synthetic cellulose conductors: microcrystalline cellulose, viscose, methylcellulose (MC
), ethylcellulose (EC), hydroxyethylcellulose (HEC), carboxymethylcellulose (CM
C).

幡 半合成海藻粘液質ニアルギン酸ナトリウム、アルギ
ン酸プロピIレンゲリコールエステル等。
Hata: Semi-synthetic seaweed mucilage sodium nialginate, alginate propylene gellicol ester, etc.

(閃 半合成蛋白質:カゼインナトリウム。(Semi-synthetic protein: Sodium caseinate.

(×)、半合成デンプン誘導体:可溶性デンゾ/、カル
ボキシメチルデンプン(CMS)、IJン酸デンプ、ン
、ジアルデヒドデンプン、ンクロデキストリン等。
(×), Semi-synthetic starch derivatives: soluble Denzo/, carboxymethyl starch (CMS), IJ acid starch, N, dialdehyde starch, nclodextrin, etc.

(XI)  合成品:ポリビニルアルコール(PVA)
、ポリアクリル酸ナトリウム、ポリエチレンオキシド等
(XI) Synthetic product: polyvinyl alcohol (PVA)
, sodium polyacrylate, polyethylene oxide, etc.

以上の高分子物質の中で目的上特に好適なのは乳化安定
作用が強い割に粘度が比較的低く、かつ耐塩性が強く、
シかもゲル化作用の弱いものである。この条件を充たす
ものとして、例、えばグアガム、タマリンドガム、カラ
ギーナン、ファーセラン、アルギン酸ナトリウム、トラ
ガントガム、アラビアゴム、アラビノガラクタン、LM
ペクチン、キサンタンガム、カゼインナトリウム、カル
ボキシメチルセルローズ等がある。
Among the above-mentioned polymer substances, those which are particularly suitable for the purpose have a strong emulsion stabilizing effect, a relatively low viscosity, and a strong salt resistance.
It also has a weak gelling effect. Examples of substances that meet this condition include guar gum, tamarind gum, carrageenan, furcelan, sodium alginate, gum tragacanth, gum arabic, arabinogalactan, LM
Examples include pectin, xanthan gum, sodium caseinate, and carboxymethyl cellulose.

高分子物質は組成物中に0.励〜5.0%、好ましくは
0.3〜2.0%の範囲で添加される。0.1%未満で
は充分な安定性が得られず、また5%超過では組成物の
粘度が高くなり過ぎて流動しにくくなる。但しこの上限
値は一応の目安であって、例えば、アラビアゴムのよう
に粘度の低い高分子物質の場合には、より濃度が高くて
も充分流動性がある。
The polymeric substance is present in the composition with 0. It is added in an amount of 5.0% to 5.0%, preferably 0.3 to 2.0%. If it is less than 0.1%, sufficient stability cannot be obtained, and if it exceeds 5%, the viscosity of the composition becomes too high and it becomes difficult to flow. However, this upper limit is just a guideline; for example, in the case of a polymeric substance with low viscosity such as gum arabic, it has sufficient fluidity even at a higher concentration.

本発明洗浄剤は、必須成分としてのアルカリ性物質及び
水溶性高分子物質の他、非イオン界面活性剤、キレート
化合物、ビルダー等の一般成分ならび媒質としての水と
から構成される。例えばアルカリ性物質としては苛性ア
ルカリ、炭酸アルカリ、ケイ酸・ナトリウム等の強アル
カリ性物質が用いられ、また非イオン界面活性剤として
は、例えばポリオキシエチレンアルキルフェノール、ポ
リオキシエチレン脂肪アルコール、ポリオキシエチレン
脂肪酸、ポリオキシエチレン酸アミド、ポリプロピレン
グリコール、ポリプロピレングリコールのブロックポリ
マー等が好適番こ利用される。非イオン界面活性剤はな
るべ(HLBの高い方が好ましい。なおまたキレート化
合物としては、ニトリロ三酢酸、エチレンジアミン四酢
酸、ジエチレントリアミン五酢酸又はこれらの塩類が使
用される。さらに本発明におけるビルダーとしては、好
ましくは無機アルカリ性塩及び中性塩ならびに有機アル
カリ性塩及び中性物質が用いられ、それらの例を挙げれ
ば、例えばリン酸ナトリウム、リン酸水素ナトリウム、
ポリリン酸ナトリウム、炭酸ナトリウム、セスキ炭酸ナ
トリウム、水ガラス、硫酸ナトリウム、塩化ナトリウム
、クエン酸ナトリウム、脂肪酸アミド、ナフタリンスル
ホン酸ナトリウムなどがある。
The cleaning agent of the present invention is composed of an alkaline substance and a water-soluble polymer substance as essential components, as well as general components such as a nonionic surfactant, a chelate compound, and a builder, and water as a medium. For example, strong alkaline substances such as caustic alkali, alkali carbonate, and sodium silicate are used as alkaline substances, and examples of nonionic surfactants include polyoxyethylene alkylphenol, polyoxyethylene fatty alcohol, polyoxyethylene fatty acid, Polyoxyethylene acid amide, polypropylene glycol, block polymers of polypropylene glycol, and the like are preferably used. The nonionic surfactant is preferably one with a high HLB (the higher the HLB is, the better. As the chelate compound, nitrilotriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, or salts thereof are used. Furthermore, as the builder in the present invention, , preferably inorganic alkaline and neutral salts and organic alkaline salts and neutral substances, such as, for example, sodium phosphate, sodium hydrogen phosphate,
Examples include sodium polyphosphate, sodium carbonate, sodium sesquicarbonate, water glass, sodium sulfate, sodium chloride, sodium citrate, fatty acid amide, and sodium naphthalene sulfonate.

以下本発明の実施例を示すが、これは例示であって、発
明の技術的範囲を限るものではない。
Examples of the present invention will be shown below, but these are merely illustrative and do not limit the technical scope of the invention.

実施例1 下表−1配合に従って標準液状アルカリ洗浄剤組成物を
作った。
Example 1 A standard liquid alkaline detergent composition was prepared according to the formulation in Table 1 below.

以上の基本組成物(配合A)に、下表−2のとおり種々
の水溶性高分子化合物を配合した。
Various water-soluble polymer compounds were blended into the above basic composition (Formulation A) as shown in Table 2 below.

(添加量は配合A−B共に同じ) 表−2 ※ポリオキージエチレンアルキルフェニルエーテルサル
フェートのナトリウム塩 囚 安定度試験 以上の各試験料を、室温(25℃)下に7日間放置して
缶液の安定度を観察した。結果は下表−3のとおりであ
った。
(The amount added is the same for both formulations A and B.) Table 2 * Sodium salt of polyoxyethylene alkyl phenyl ether sulfate Each test material that passed the stability test was left at room temperature (25°C) for 7 days and the can liquid was The stability of was observed. The results were as shown in Table 3 below.

表−3 〔評価基準〕 0:分離、沈澱又は析出物を認めず。Table-3 〔Evaluation criteria〕 0: No separation, precipitation or precipitate observed.

△ニゲル化発生 X:分離、沈澱又は析出物を認める。△Nigelization occurs X: Separation, precipitation, or precipitate was observed.

上表−3が示す如く、牛サンタンガム又はそれとアルギ
ン酸ナトリウムもしくはCMCナトリウム、CMC−ナ
トリウムあるいはCMC−ナトリウムとアニオン界面活
性剤とを含む本発明品1〜5は、高分子化合物の量が0
.5〜1.2%の範囲内で組成物が安定化されているこ
とが示される。これに反し、キサンタンガム又はポリビ
ニルアルコールを0.05又+i o、os%含有含有
比較量l及び2では安定化効果が不充分であり、またC
 M C−Na又はそれと可溶性デンプンを6%含む比
較量3及び4ではゲル化が発生し、商品として不適当と
なる事実が示される。因みに、本実験で用いたキサンタ
ンガムはD−グルコース、D−マンノース及びD−グル
クロン酸が鎖状に結合したものであり、またCMCはD
−グルコースのみが直鎖状に結合した化合物を骨幹とす
るものであり、さらにアルギン酸はD−マンノウロン酸
の直鎖状結合体であるから、これらはいづれも化学的に
異質のものということができ、従って水溶性高分子物質
の化学構造如何は、発明効果に対し余り影智を与えない
であろうことが推測される。なお、この実験の結果から
見て、組成物中における水溶性高分子物質の含量は、0
,1%以上5%以下、好ましくは0.3〜2.0%の範
囲内に在ることが適当であろう。
As shown in Table 3 above, products 1 to 5 of the present invention containing bovine suntan gum or it and sodium alginate or sodium CMC, sodium CMC, or sodium CMC and an anionic surfactant have a polymer compound content of 0.
.. It is shown that the composition is stabilized within the range of 5-1.2%. On the other hand, when the comparative amounts 1 and 2 containing xanthan gum or polyvinyl alcohol at 0.05% or +IO, os%, the stabilizing effect was insufficient, and C
Comparative amounts 3 and 4 containing MC-Na or 6% soluble starch caused gelation, indicating the fact that they were unsuitable for commercial use. Incidentally, the xanthan gum used in this experiment is D-glucose, D-mannose, and D-glucuronic acid linked together in a chain, and CMC is D-glucuronate.
-Since only glucose is the backbone of a compound that is linked in a linear chain, and alginic acid is a linear combination of D-mannouronic acid, they cannot be said to be chemically different. Therefore, it is presumed that the chemical structure of the water-soluble polymer substance does not have much influence on the effectiveness of the invention. In addition, from the results of this experiment, the content of water-soluble polymeric substance in the composition is 0.
, 1% to 5%, preferably 0.3 to 2.0%.

実施例2 前例で用いた標準液状アルカリ洗浄剤組成物(配合A)
に次の処置を加えた。
Example 2 Standard liquid alkaline cleaning composition used in the previous example (formulation A)
The following actions were taken.

(イ) 比較量イ:ハイドロトロピー剤として、ポリオ
キシエチレンアルキルフェニルエーテルホスフェートの
ナトリウム塩0.5%を添加。
(A) Comparative amount A: 0.5% of sodium salt of polyoxyethylene alkylphenyl ether phosphate was added as a hydrotropic agent.

(ロ) 比較量ロ:ハイドロトロピー剤として、インプ
ロパツール1%を添加。
(b) Comparative amount b: Added 1% Impropatool as a hydrotropic agent.

(ハ) 比較量ハ:非イオン界面活性剤のHLBをIO
に変更。
(c) Comparative amount c: HLB of nonionic surfactant is IO
change to.

に) 比較品二二ビルダ一部及びキレート部(粒状固形
物)点界面活性5部(液状)とに分離O なお、別に、本発明品5の安定剤中、アニオン界面活性
剤をカゼイン4%に変更した発明品5′を作った。
) Comparative product 22 builder part and chelate part (granular solid matter) point surface active part separated into 5 parts (liquid) O Separately, in the stabilizer of invention product 5, the anionic surfactant was 4% casein. Invention 5' was created by changing the .

以上の比較品イ〜二と本発明品l及び5と安定性、洗浄
性、起泡性及び作業性の各点につき対比した。結果を下
表−4として示す。
Comparative products A to II and products I and V of the present invention were compared in terms of stability, washability, foaming performance, and workability. The results are shown in Table 4 below.

注1)安定性の評価 O:1週間以上安定 △:1週間週間未定 安定1週間未満に分離 注2)洗浄性の評価 (al  被洗浄物 市販のテストピースに、モーピル油#−5080部及び
大豆油20部からなる鉱物油・油脂混合物中に浸漬した
0紙を交互に重ね合わせ、100℃において100cj
Aの圧力下に3時間放置後、0紙を除き試験に供する。
Note 1) Stability evaluation O: Stable for more than 1 week △: 1 week undetermined stable Separated in less than 1 week Note 2) Cleanability evaluation (al) Item to be cleaned A commercially available test piece was coated with 80 parts of Mopil Oil #-50 and 0 paper soaked in a mineral oil/fat mixture consisting of 20 parts of soybean oil was layered alternately and heated to 100 cj at 100°C.
After leaving under the pressure of A for 3 hours, remove the 0 paper and use it for the test.

(bl  洗浄条件 極性カソード処理による電解洗浄法を採用、電流密度4
 fiy’M 、  電解時間3秒、洗浄剤濃度3oy
ie(固形分として)、洗浄温度70℃。
(bl Cleaning conditions Adopts electrolytic cleaning method with polar cathode treatment, current density 4
fiy'M, electrolysis time 3 seconds, cleaning agent concentration 3oy
ie (as solid content), washing temperature 70°C.

(cl  評価方法 被洗浄鉄板の水濡れ面M(%)を測定、算出。(cl evaluation method Measure and calculate the water wet surface M (%) of the iron plate to be cleaned.

注3)起泡性 洗浄液各50−を1004容のネスラー管に採り、20
0陣令の割合で激しく振盪し、発生した泡量をd数で現
わす。
Note 3) Pour 50 μl of each foaming cleaning solution into a 1004 volume Nessler tube, and add 20
Shake vigorously at a rate of 0 and the amount of bubbles generated is expressed as d number.

注4)作業性の評価 O:作業性良好 ×:作業性不良 以上の実験結果が示すように、ハイドロトロピー剤とし
てアニオン界面活性剤を加えた比較量イは安定性が悪い
上に起泡性が大きく、しかも洗浄性が余り良くない。ハ
イドロトロピー剤としてインプロパツールを加えた比較
品口は安定性が極めて悪く、本組成のような高濃度液状
洗浄剤に対しては実質的にハイドロトロープ効果のない
ことが判る。非イオン界面活性剤のHLBを低下させた
比較量ノ・の洗浄性は著しく悪く、通説どおりHLBと
洗浄性との相関を裏付けている。しかも安定性はそれ程
向上していない。ビルグ一部と界面活性剤とを分離した
比較品二の安定性が良いことは当然であるが、作業性が
劣ることは云うまでもない。
Note 4) Evaluation of workability O: Good workability ×: Poor workability As shown in the above experimental results, the comparative amount A, in which an anionic surfactant was added as a hydrotropic agent, had poor stability and foaming properties. is large, and the cleaning properties are not very good. It can be seen that the comparative product containing Impropatool as a hydrotropic agent has extremely poor stability and has virtually no hydrotropic effect on a highly concentrated liquid detergent such as the present composition. The detergency of the comparative amount of nonionic surfactant with lower HLB was significantly poorer, which supports the correlation between HLB and detergency, as is commonly believed. Moreover, the stability has not improved that much. It goes without saying that Comparative Product 2, in which part of the bilge and the surfactant are separated, has good stability, but it goes without saying that the workability is inferior.

以上に反し、高分子化合物を含む発明品lと5′はいづ
れも安定で、洗浄性も比較品二と同等か又はそれより優
れており、かつ起泡性もそれ程大きくなく、シかも作業
性に優れているので、液状アルカリ洗浄剤として優秀で
ある。なお、発明品lの洗浄性が同5′に比し優れてい
るのは、恐らくキサンタンガムの持つ大きな乳化粒子を
作る特性と相関しているよ1  うに思われる。
Contrary to the above, both invented products 1 and 5', which contain polymer compounds, are stable, have the same or better cleaning properties than comparative product 2, and have not so large foaming properties, and are easy to work with. It is excellent as a liquid alkaline cleaning agent. The superior detergency of Inventive Product 1 compared to Inventive Product 5' probably correlates with the property of xanthan gum to form large emulsified particles.

以上詳述したように、本願発明は、産業用の液状洗剤に
おける安定性上の欠点を完全に解決し得たものであって
、液状洗浄剤の利点を最大限度に発揮させるから、洗剤
利用者に多大の便益をもたらすものである。
As described in detail above, the present invention completely solves the stability disadvantages of industrial liquid detergents, and maximizes the advantages of liquid detergents, so it is useful for detergent users. It brings great benefits to the world.

Claims (1)

【特許請求の範囲】 ill  必須の安定剤成分として、水溶性高分子物質
を含有する液状アルカリ洗浄剤。 (2)  水溶性高分子物質が、組成物中に0.1〜5
.0%、好ましくは0.3〜2.0%の範囲内で存在す
る液状アルカリ洗浄剤。
[Claims] ill A liquid alkaline detergent containing a water-soluble polymeric substance as an essential stabilizer component. (2) The composition contains 0.1 to 5 water-soluble polymeric substances.
.. A liquid alkaline cleaning agent present in an amount of 0%, preferably in the range of 0.3-2.0%.
JP17364081A 1981-10-28 1981-10-28 Liquid alkali detergent Granted JPS5874800A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17364081A JPS5874800A (en) 1981-10-28 1981-10-28 Liquid alkali detergent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17364081A JPS5874800A (en) 1981-10-28 1981-10-28 Liquid alkali detergent

Publications (2)

Publication Number Publication Date
JPS5874800A true JPS5874800A (en) 1983-05-06
JPH0433840B2 JPH0433840B2 (en) 1992-06-04

Family

ID=15964350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17364081A Granted JPS5874800A (en) 1981-10-28 1981-10-28 Liquid alkali detergent

Country Status (1)

Country Link
JP (1) JPS5874800A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4652393A (en) * 1983-09-02 1987-03-24 Research Chemical Coating remover and wood restorative compositions and methods of using same
US4734138A (en) * 1985-05-13 1988-03-29 Research Chemical Method of removing coating and restoring wood
JP2001003098A (en) * 1999-06-24 2001-01-09 Toho Chem Ind Co Ltd Detergent composition for removing fine particles excellent in rinsability
US6236043B1 (en) 1997-05-09 2001-05-22 Hitachi, Ltd. Electromagnet and magnetic field generating apparatus

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52123407A (en) * 1976-04-08 1977-10-17 Yuken Kogyo Co Ltd Detergent composition
JPS5346303A (en) * 1976-10-08 1978-04-25 Sanpooru Kk Liquid cleanser
JPS5360909A (en) * 1976-11-12 1978-05-31 Minoru Sakamoto Continuous burning kiln capable to couple and separate
JPS5366909A (en) * 1976-04-01 1978-06-14 Unilever Nv Aqueous builder added liquid detergent compositions and production thereof
JPS5429303A (en) * 1977-08-06 1979-03-05 Earth Chemical Co Liquid detergent compositions

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5366909A (en) * 1976-04-01 1978-06-14 Unilever Nv Aqueous builder added liquid detergent compositions and production thereof
JPS52123407A (en) * 1976-04-08 1977-10-17 Yuken Kogyo Co Ltd Detergent composition
JPS5346303A (en) * 1976-10-08 1978-04-25 Sanpooru Kk Liquid cleanser
JPS5360909A (en) * 1976-11-12 1978-05-31 Minoru Sakamoto Continuous burning kiln capable to couple and separate
JPS5429303A (en) * 1977-08-06 1979-03-05 Earth Chemical Co Liquid detergent compositions

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4652393A (en) * 1983-09-02 1987-03-24 Research Chemical Coating remover and wood restorative compositions and methods of using same
US4734138A (en) * 1985-05-13 1988-03-29 Research Chemical Method of removing coating and restoring wood
US6236043B1 (en) 1997-05-09 2001-05-22 Hitachi, Ltd. Electromagnet and magnetic field generating apparatus
US6365894B2 (en) 1997-05-09 2002-04-02 Hitachi, Ltd. Electromagnet and magnetic field generating apparatus
JP2001003098A (en) * 1999-06-24 2001-01-09 Toho Chem Ind Co Ltd Detergent composition for removing fine particles excellent in rinsability

Also Published As

Publication number Publication date
JPH0433840B2 (en) 1992-06-04

Similar Documents

Publication Publication Date Title
NO151327B (en) WATER-FREE, CONSTRUCTED, LIQUID DETERGENT MIXTURE, AND PROCEDURE FOR PREPARING SUCH A
JP2005504630A5 (en)
JPH08501120A (en) Improved hard surface detergent
CA1209011A (en) Water-in-oil emulsions having improved low temperature properties
US4153571A (en) Heat dependent alkali gel cleaning compositions and process for cleaning greasy surfaces
JPS5874800A (en) Liquid alkali detergent
JPS60186600A (en) Bl eaching composition
CN106893115A (en) A kind of high concentration non-ionic celluloses ether suspended dispersed liquid and preparation method thereof
Sawicki Impact of surfactant composition and surfactant structure on foam control performance
JP2009298955A (en) Method of manufacturing cooling agent
CN110724607B (en) Shower room cleaning cream and preparation method thereof
EP0758352A1 (en) Aqueous suspension of a cellulose ether, method for the production thereof, and composition
CN1361819A (en) Liquid abrasive cleaning composition
CN113652236B (en) Mudstone dispersant and preparation method thereof
US3296147A (en) Cleaner for food residues
JPS6148546B2 (en)
JP3370185B2 (en) High-concentration one-part alkaline detergent composition and method for producing the same
JP2004518009A (en) Drag reduction of heat distribution water-based liquid containing large amount of antifreeze
JP2001524589A5 (en)
CN113150879A (en) Thickening composition for washing effervescent tablets and washing effervescent tablets
JP2004518010A (en) Use of Zwitterionic Surfactants as Anionic Ether-Containing Surfactants as Drag Reduction Agents
CN113385103A (en) Surfactant composition, preparation method and application
JP3250857B2 (en) Method for producing high-concentration surfactant paste
JPH0680996A (en) Lowly foaming detergent
JP3106016B2 (en) Low foam neutral detergent