JPH0433840B2 - - Google Patents

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Publication number
JPH0433840B2
JPH0433840B2 JP56173640A JP17364081A JPH0433840B2 JP H0433840 B2 JPH0433840 B2 JP H0433840B2 JP 56173640 A JP56173640 A JP 56173640A JP 17364081 A JP17364081 A JP 17364081A JP H0433840 B2 JPH0433840 B2 JP H0433840B2
Authority
JP
Japan
Prior art keywords
sodium
alkaline
water
present
liquid
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.)
Expired - Lifetime
Application number
JP56173640A
Other languages
Japanese (ja)
Other versions
JPS5874800A (en
Inventor
Takeshi Kono
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

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はアルカリ洗浄剤、殊に安定性及び洗浄
性等に優れた金属、プラスチツクス用アルカリ洗
浄剤に関する。 今日、金属類、プラスチツクス等へのメツキ、
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、アルカリ金属の
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つて、今日使用
される洗浄剤の中、過半量はビルダー成分などに
界面活性剤を被覆、含浸等の手段で配合、乾燥さ
せた粉状又は紛状のものである。 しかし紛状、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、塩折効果
の関係で界面活性剤が分離、折出しやすいため、
高濃度のものを得難いという、製造上の難点を有
する。本発明は、金属、プラスチツクス用液状ア
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。 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、 (1) 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(Hydrotropic action,溶解度増大作用)
を利用する方法。 (2) 界面活性剤のHLB値を低下させる方法。 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。 などが知られている。 しかし、(1)のハイドロトロピー作用を利用する
方法では、性能の低下及び殊ひアニオン界面活性
剤が添加された場合にはそれによる発泡性の増大
が問題となつて来る。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折出防止手
段はいづれも効果において不満足であつて、この
ことが液状洗浄剤の発展を妨げる原因となつてい
た。 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が、特に
キサンタンガム、カルボキシメチルセルロース又
はその塩及びアルギン酸塩(以下「水溶性高分子
物質」又は単に、「高分子物質」と呼ぶ)が強い
安定性作用を奏することを見出した。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つ
て、これらコロイド物質の存在が難溶性物質の折
出及至沈澱防止に奏効することは周知のことであ
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折
出防止作用を奏するであることは簡単に予測でき
ないことであつて、本発明者により始めて見出さ
れた新知見である。 上記水溶性高分子物質は組成物中に0.1〜5.0
%、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効果が得られず、また
5%超過では一般に組成物の粘度が高くなつて流
動しにくくなる。 本発明の液状アルカリ洗浄剤は、必須成分とし
ての水溶性高分子物質の他、慣用成分としてのア
ルカリ性物質、非イオン界面活性剤、キレート化
合物、ビルダー、水などの一般成分を含む。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エノー
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
グリコールのブロツクポリマー等が好適に利用さ
れる。非イオン界面活性剤はなるべく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、リン酸水素ナトイウム、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。 以下本発明の実施例を示すが、これは例示であ
つて、発明の技術的範囲を限るものではない。 実施例 1 下表―1配合に従つて標準液状アルカリ洗浄組
成物を作つた。
The present invention relates to an alkaline cleaning agent, particularly an alkaline cleaning agent for metals and plastics having excellent stability and cleaning properties. Today, plating metals, plastics, etc.
Large amounts of alkaline cleaning agents are consumed in preparatory work such as painting. These alkaline cleaning agents are
Generally, alkali metal hydroxides, neutral salts of alkali metals, chelating agents, various builders and surfactants are blended, and the majority of cleaning agents used today are builder components. It is a powder or fine powder obtained by coating, impregnating, etc. with a surfactant and drying it. However, in addition to being bulky, solid products such as powders 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, liquids have advantages over the former, such as being easy to measure and can be transported through pipes, but on the other hand, surfactants tend to separate and precipitate due to the salt folding effect.
It has manufacturing difficulties in that it is difficult to obtain high-concentration products. The present invention relates to a new detergent composition that solves the above-mentioned problems in liquid alkaline detergents for metals and plastics. Conventionally, as an attempt to stably incorporate surfactants into alkaline aqueous solutions, (1) hydrotropic action (solubility increasing action) on anionic surfactants or nonionic surfactants such as lower alcohols;
How to use. (2) A method to reduce the HLB value of surfactants. and (3) two alkaline cleaning agents (one liquid, one
The other is a method of dividing into liquid or powder. etc. are known. However, in the method (1) that utilizes hydrotropy, problems arise such as a decrease in performance and an increase in foaming properties, especially when an anionic surfactant is added. Furthermore, according to the method (2) of lowering the HLB, cleaning performance is sacrificed. moreover
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. However, as a result of conducting systematic research on means for preventing the precipitation phenomenon in liquid alkaline cleaning agents, the present inventor has recently discovered that many water-soluble polymeric substances are extremely useful for this purpose. It has been found that xanthan gum, carboxymethylcellulose or a salt thereof, and alginate (hereinafter referred to as "water-soluble polymeric material" or simply "polymeric material") exhibit a strong stabilizing effect. 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 and precipitation of poorly soluble substances, but this is the subject of the present invention. The fact that a strong anti-precipitation effect can be achieved in a strongly alkaline 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. The above water-soluble polymeric substance is present in the composition in an amount of 0.1 to 5.0.
%, preferably in the range of 0.3 to 2.0%.
If it is less than 0.1%, a sufficient stabilizing effect will not be obtained, and if it exceeds 5%, the viscosity of the composition will generally increase and it will become difficult to flow. The liquid alkaline detergent of the present invention contains general components such as an alkaline substance, a nonionic surfactant, a chelate compound, a builder, and water as conventional components in addition to a water-soluble polymeric substance as an essential component. 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 alkylphenols, polyoxyethylene fatty alcohols, and polyoxyethylene fatty acids. , polyoxyethylene acid amide, polypropylene glycol, block polymers of polypropylene glycol, etc. are suitably used. It is preferable for the nonionic surfactant to have a high HLB. In addition, chelate compounds include nitrilotriacetic acid, ethylenediaminetetraacetic acid,
Diethylenetriaminepentaacetic acid or salts thereof are used. Further, as the builder in the present invention, inorganic alkaline salts and neutral salts and organic alkaline salts and neutral substances are preferably used, such as sodium phosphate, sodium hydrogen phosphate, sodium polyphosphate, sodium carbonate, sodium sesquicarbonate,
These include water glass, sodium sulfate, sodium chloride, sodium citrate, fatty acid amide, and sodium naphthalene sulfonate. Examples of the present invention will be shown below, but these are merely illustrative and do not limit the technical scope of the invention. Example 1 A standard liquid alkaline cleaning composition was prepared according to the formulation in Table 1 below.

【表】 以上の基本組成物(配合A及びB)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。 (添加量は配合A・B共に同じ)
[Table] The following table -
Various water-soluble polymer compounds were blended as shown in 2. (The amount added is the same for both formulations A and B)

【表】【table】

【表】 * ポリオキシエチレンアルキルフエニルエ
ーテルサルフエートのナトリウム塩
A 安定度試験 以上の各試験料を室温(25℃)下に7日間放置
して各液の安定度を観察した。結果は下表―3の
とおりであつた。
[Table] * Polyoxyethylene alkyl phenyl
Sodium Salt A of Tersulfate Stability Test Each of the above test materials was left at room temperature (25°C) for 7 days and the stability of each solution was observed. The results were as shown in Table 3 below.

【表】 上表―3が示す如く、キ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又は0.08%含有する比較品1及び2では安
定化効果が不充分であり、またCMC―Na又はそ
れと可溶性デンプンを6%含む比較品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、従つ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響を与えないであ
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。 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,但し水溶性高分子物質を含まず)に次
を処置を加えた。 (イ) 比較品イ: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エニルエーテルホス
フエートのナトリウム塩0.5%を添加。 (ロ) 比較品ロ:ハイドロトロピー剤として、イソ
プロパノール1%を添加。 (ハ) 比較品ハ:非イオン界面活性剤のHLBを10
に変更。 (ニ) 比較品ニ:ビルダー部及びキレート部(粒状
固形物)と界面活性部(液状)とに分離。 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
作つた。 以上の比較品イ〜ニと本発明品1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。
[Table] As shown in Table 3 above, products 1 to 5 of the present invention containing xanthan gum or it, sodium alginate or CMC sodium, CMC-sodium or CMC-sodium, and an anionic surfactant
It is shown that the composition is stabilized when the amount of the polymer compound is within the range of 0.5 to 1.2%. On the other hand, Comparative Products 1 and 2 containing 0.05 or 0.08% xanthan gum or polyvinyl alcohol had insufficient stabilizing effect, and Comparative Products 3 and 4 containing 6% CMC-Na or soluble starch with CMC-Na caused gelation. This indicates the fact that this occurs and the product is unsuitable for use as a product. Incidentally, the xanthan gum used in this experiment contains D-glucose, D-mannose, and D-
Glucuronic acid is linked in a chain, and
CMC is composed of a compound in which only D-glucose is linked in a linear chain, and alginic acid is a linear linkage of D-mannouronic acid, so they are both chemically different. Therefore, it is presumed that the chemical structure of the water-soluble polymer substance will not have much influence on the effectiveness of the invention. In addition, in view of the results of this experiment, the content of the water-soluble polymeric substance in the composition is 0.1% or more and 5% or less, preferably 0.3 to 2.0%.
It would be appropriate to be within the range of Example 2 The following treatments were added to the standard liquid alkaline cleaning composition (Formulation A, but containing no water-soluble polymeric substance) used in the previous example. (A) Comparative product A: 0.5% sodium salt of polyoxyethylene alkyl phenyl ether phosphate was added as a hydrotropic agent. (B) Comparative product B: 1% isopropanol was added as a hydrotropic agent. (c) Comparative product c: HLB of nonionic surfactant is 10
change to. (d) Comparative product d: Separated into builder part and chelate part (granular solid) and surface active part (liquid). Separately, Invention Product 5' was prepared by changing the anionic surfactant in the stabilizer of Invention Product 5 to 4% casein. Comparative products 1 to 2 and products 1 and 5 of the present invention were compared in terms of stability, washability, foaming property, and workability. The results are shown in Table 4 below.

【表】 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品イ
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
イソプロパノールを加えた比較品ロは、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
せた比較品ハ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れいる。しかも
安定性はそれ程向上していない。ビルダー部と界
面活性剤とを分離した比較品ニの安定性が良いこ
とは当然であるが、作業性が劣ることは云うまで
もない。 以上に反し、高分子化合物を含む発明品1と5´
はいづれも安定で、洗浄性も比較品ニと同等か又
はそれより優れており、かつ起泡性もそれ程大き
くなく、し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1
の洗浄性が同5´に比し優れているのでは、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
と相関しているように思われる。 以上詳述したように、本願発明は、金属及びプ
ラスチツクスを対象とする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つて、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。
[Table] As shown by the above experimental results, Comparative Product A, in which an anionic surfactant was added as a hydrotropic agent, had poor stability, large foaming properties, and poor cleaning properties. Comparative product B, in which isopropanol was added as a hydrotropic agent, had extremely poor stability and was found to have virtually no hydrotropic effect on high-concentration liquid detergents such as the present composition. Comparative product C, which is a nonionic surfactant with a lower HLB, has significantly poor cleaning performance, as is commonly believed.
This proves the correlation between HLB and cleanability. Moreover, the stability has not improved that much. It goes without saying that the comparative product 2, in which the builder part and the surfactant are separated, has good stability, but it goes without saying that the workability is inferior. Contrary to the above, invention products 1 and 5' containing polymer compounds
All of them are stable, their cleaning properties are equal to or better than comparative product 2, their foaming properties are not so large, and they are excellent in workability, so they are excellent as liquid alkaline cleaning agents. In addition, invention 1
The superior detergency of 5' compared to 5' is probably related to the ability of xanthan gum to form large emulsified particles. As detailed above, the present invention completely solves the stability disadvantages of liquid detergents for metals and plastics, and maximizes the advantages of liquid detergents. This brings great benefits to detergent users.

Claims (1)

【特許請求の範囲】 1 安定化剤としてキサンタンガム、カルボキシ
メチルセルロース又はその塩及びアルギン酸塩か
ら選ばれた水溶性高分子物質を含有することを特
徴とする安定な金属・プラスチツクス用液状アル
カリ洗浄剤。 2 水溶性高分子物質が、洗浄剤組成物中に0.1
〜5%、好ましくは0.3〜2%の割合で存在する
特許請求の範囲第1項記載のアルカリ洗浄剤。
[Scope of Claims] 1. A stable liquid alkaline cleaning agent for metals and plastics, characterized in that it contains a water-soluble polymeric substance selected from xanthan gum, carboxymethyl cellulose or its salt, and alginate as a stabilizer. 2 The water-soluble polymer substance is contained in the cleaning composition at a concentration of 0.1
Alkaline detergent according to claim 1, present in a proportion of ~5%, preferably 0.3-2%.
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 JPS5874800A (en) 1983-05-06
JPH0433840B2 true 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)

Families Citing this family (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
JP2978873B2 (en) 1997-05-09 1999-11-15 株式会社日立製作所 Electromagnet and accelerator, and accelerator system
JP2001003098A (en) * 1999-06-24 2001-01-09 Toho Chem Ind Co Ltd Detergent composition for removing fine particles excellent in rinsability

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

Also Published As

Publication number Publication date
JPS5874800A (en) 1983-05-06

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