JPH0357958B2 - - Google Patents

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Publication number
JPH0357958B2
JPH0357958B2 JP60226672A JP22667285A JPH0357958B2 JP H0357958 B2 JPH0357958 B2 JP H0357958B2 JP 60226672 A JP60226672 A JP 60226672A JP 22667285 A JP22667285 A JP 22667285A JP H0357958 B2 JPH0357958 B2 JP H0357958B2
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JP
Japan
Prior art keywords
weight
composition
carbon atoms
composition according
aliphatic
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
JP60226672A
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Japanese (ja)
Other versions
JPS6197395A (en
Inventor
Fuinsento Bosukanpu Ieerusu
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.)
Unilever NV
Original Assignee
Unilever NV
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Filing date
Publication date
Application filed by Unilever NV filed Critical Unilever NV
Publication of JPS6197395A publication Critical patent/JPS6197395A/en
Publication of JPH0357958B2 publication Critical patent/JPH0357958B2/ja
Granted legal-status Critical Current

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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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/37Mixtures of compounds all of which are anionic
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/06Ether- or thioether carboxylic acids
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

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  • 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)
  • Detergent Compositions (AREA)

Abstract

The invention pertains to suspending aqueous built liquid detergent composition comprising an anionic detergent active, electrolyte salts and a fatty alcohol polyalkylene oxide, carboxylate salt. Inclusion of the carboxylate salt renders the rheology of the composition less sensitive to electrolyte materials.

Description

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

本発明は液体洗剤組成物、特に洗浄作用性を有
し且つ不溶物質を懸濁し得る懸濁システムからな
る水性ビルダー入り液体洗剤組成物(aqueous
builtliquid detergent compositions)に係る。 水性ビルダー入り液体洗剤組成物は良く知られ
ており、極めて多くの配合物が先行技術で開示さ
れてきた。この種の組成物は通常1種以上の洗浄
作用化合物と1種以上のビルダー塩とを不溶のビ
ルダー及び/又は補助物質(adjuvant
materials)を懸濁し得る水性媒体中に含んで構
成される。 しかしながら、この種の従来型のビルダー入り
液体洗剤は電解質レベルに対する感度
(sensitivity)が著しく大きいという重大な欠点
を有する。このような感敏性を有すると、物理的
に安定な組成の範囲及び許容し得る粘性の範囲の
大きさと位置とが溶解電解質量に応じて大きく変
化することになる。特にNTAの如き可溶性のよ
り高いビルダーを大量に使用すると、通常は液体
が不安定になり沈殿又は相分離を生起し易くな
る。 以上の理由から本発明の目的は、電解質物質に
対する感度がより低く、この種の物質をより大量
に使用しても粘性が許容し得るものであるような
前述タイプの組成物を提供することである。 従来の陰イオン表面活性物質の一部分を任意
に、特定の脂肪アルコールポリグリコールエーテ
ル誘導陰イオン表面活性剤を比較的少量用いて代
替すると、電気質物質特にビルダー及び単純な電
解質塩に対するレオロジー上の感度が低下するこ
とが判明した。 そこで本発明は、合成陰イオン系洗浄作用物質
と電解質塩とを含み、次式 R−(OCoH2ox−O(CH2y−COOM 〔式中Rは炭素原子を8〜20個を有する脂肪族
炭化水素基、又は脂肪族部分に4〜20個の炭素原
子を有する脂肪族−芳香族炭化水素基を表わし、
nは2から3までの数であり、xは1から16まで
の数であり、yは0から2までの数であり、Mは
陽イオンである〕 で示される脂肪アルコールポリアルキレンオキサ
イドカルボン酸塩又はこれら塩の混合物を0.5〜
10重量%含むことを特徴とする粒状物質懸濁作用
のある水性ビルダー入り液体洗剤組成物を提供す
る。 本発明のアルキルポリアルキレンオキサイドカ
ルボン酸塩は次式 R−(OCoH2ox−O(CH2y−COOM で示されることを特徴とする。 上記式中Rは炭素原子を8〜20個有する脂肪族
炭化水素であり、又は脂肪族部分に4〜20個の炭
素原子を有する脂肪族−芳香族炭化水素でもあり
得る。Rは通常直鎖又は分岐状、飽和又は不飽和
の種々の長さの脂肪族炭化水素基の混合物からな
り、好ましくは炭素原子を1〜14個有する直鎖飽
和脂肪族炭化水素である。 ポリアルキレンオキサイド部分(OCoH2ox
好ましくはエチレンオキサイドユニツト(n=
2)のみを含むが、プロピレンオキサイド又はプ
ロピレンオキサイドとエチレンオキサイドとの混
合物も適切である(2<n3)。エチレン及
び/又はプロピレンオキサイドユニツトの数
(x)は1〜16、特に1〜12である。アルキレン
オキサイド部分は好ましくは2〜5個のエチレン
オキサイドユニツトを含む。 カルボン酸塩部分((CH2y−COOM)は好ま
しくはアルキル鎖を含まない(y=0)が、メチ
レン及びエチレンの如き短いアルキル鎖を含んで
もよい。Mは陽イオンであり、水素、ナトリウ
ム、カリウム、アンモニウム、モノー、ジー及び
トリエタノールアンモニウムの中から選択され、
好ましくはアルカリ金属陽イオンである。 本発明の洗剤組成物には脂肪アルコールポリア
ルキレンオキサイドカルボン酸塩又はこれら塩の
混合物が合成陰イオン系洗浄作用物質の一部分と
任意に代替すべく0.5〜10%の量で含まれる。好
ましい量はカルボン酸塩化合物を含まない組成物
のレオロジーと所望のレオロジーとに依存する。
通常は、2〜5重量%の脂肪アルコールポリアル
キレンオキサイドカルボン酸塩をほぼ等量の合成
陰イオン系洗浄作用物質に代えて使用すると最良
の結果が得られる。 本発明は特に、合成陰イオン系洗浄作用物質と
電解質塩とをベースとする水性液体ビルダー入り
組成物に適用し得る、適切な合成陰イオン系洗浄
作用物質としてはアルキルアリールスルホン酸塩
タイプ、アルキル−及びアルキルエーテル硫酸塩
タイプ、アルカン−及びアルケンスルホン酸塩タ
イプ等々の公知の陰イオン系洗剤が挙げられる。
他にも多くの例がシユワルツ、ペリー
(Schwartz,Perry)著「洗剤及び界面活性剤
(Detergents and Surface−Active Agents)」
第巻、1958年、に列挙されている。 好ましくはアルキル鎖が10〜18個の炭素原子を
有するようなアルキルアリールスルホン酸塩、例
えばn−ドデシルベンゼンスルホン酸塩、テトラ
プロピレンベンゼンスルホン酸塩、n−ペンタデ
シルベンゼンスルホン酸塩、及び脂肪族基が分解
ワツクスポリマーから得られるような直鎖C12
C15アルキルベンゼンスルホン塩酸であつて、い
ずれもナトリウム塩又はカリウム塩の形態で使用
する。 合成陰イオン系洗浄作用物質の合計量は組成物
全体の6〜12重量%である。 主要洗浄作用成分は前記陰イオン系物質である
が、他の洗浄作用物質、特に非イオン系洗浄作用
物質も少量使用し得る。非イオン系洗剤は通常、
アルキレンオキサイドと反応した疎水性部分から
成る。 適切なものとしては、1〜30モルのアルキレン
オキサイドと縮合した1級又は2級の、直鎖又は
分岐鎖のC8〜C18アルコール、1〜30モルのアル
キレンオキサイドと縮合しアルキル基が9〜18個
の炭素原子を持つモノ−もしくはジアルキルフエ
ノール、1〜30モルのアルキレンオキサイドと縮
合したC10〜C18脂肪酸モノ−もしくはジアルキル
オールアミド、異なるかもしくは同一のアルキレ
ンオキサイドのブロツクコポリマー、等々が挙げ
られる。アルキレンオキサイドは通常エチレンオ
キサイドであるが、プロピレンオキサイド、又は
エチレンオキサイドとプロピレンオキサイドとの
混合物も使用し得る。その他の適切な例はエム・
シツク(M.Schick)著「非イオン系界面活性剤
(Nonionic Surfactants)」に列挙されている。 本発明の組成物に導入し得る非イオン系洗浄作
用物質の量は5%までであるが、合成陰イオン系
洗浄作用物質の量よりは少なくしなければない。 本発明で使用する電解質は洗浄作用物質の部分
塩析を生起させるような電解質である。本発明の
組成物は通常1〜60重量%、好ましくは3〜50重
量%、特に好ましくは5〜30重量%の電解質を含
み得る。 代表的なものとしてはビルダー塩、例えばアル
カリ金属オルト−及びピロホスフエート、トリポ
リリン酸ナトリウムの如きアルカリ金属トリポリ
リン酸アンモニウム、アルカリ金属クエン酸塩、
ニトリロトリ酢酸のアルカリ金属塩並びにカルボ
キシメチルオキシコハク酸のアルカリ金属塩等が
挙げられる。 適切な電解質としてアルカノールアミンの如き
緩衝剤、特にトリエタノールアミン、アルカリ金
属カルボン酸塩、アルカリ金属ホウ酸塩、アルカ
リ金属ケイ酸塩等々も挙げられる。 本発明の組成物は更に、この種の生成物に通常
含まれる総ての成分、例えば洗浄力を増加させる
ためのアルカリ金属亜硫酸塩、単独の酵素又は例
えばホウ砂と共に用いるポリアルコール又はアル
カノールアミンのような酵素安定剤と組合わせた
酵素、螢光体、ゼオライトの如き別のビルダー、
方解石の如き研摩剤(abrasives)、よごれ懸濁
剤、再付着防止剤、ハイドロトープ、腐食抑制
剤、泡沫増加剤又は減少剤、乳濁剤(opacifing
agents)、香料、着色剤、任意に漂白剤先駆体と
組合わせた漂白剤を含み得る。 本発明の生成物は従来技術を用いて製造し得
る。この場合該生成物は後撹拌(post−stirring)
にかけるかまたはデシンテグレーター
(desintegrator)もしくは類似の高剪断装置
(high−shear exerting equipment)に通すこと
などにより製造工程の最後に最大安定粘性が得ら
れるまで剪断すると有利であることが判明した。
このように処理した生成物は吸入排出操作
(pumping)及び壜詰操作の間に更に剪断力
(shear)が加えられても粘性への影響を受けな
い。 次に実施例を挙げて本発明を説明する。ここに
示す%はいずれも最終組成物に対する重量%であ
る。 実施例 表1に記載の配合に従つて、物理的安定性が高
く、高電解質レベルに対して明らかにより高い許
容性(tolerance)を示す組成物を製造した。
The present invention relates to liquid detergent compositions, in particular aqueous built liquid detergent compositions having detergent properties and comprising a suspension system capable of suspending insoluble substances.
(builtliquid detergent compositions). Aqueous built liquid detergent compositions are well known and numerous formulations have been disclosed in the prior art. Compositions of this type usually contain one or more detergent compounds and one or more builder salts, insoluble builder and/or adjuvant substances.
materials) in an aqueous medium in which they can be suspended. However, conventional built liquid detergents of this type have a significant drawback of significant sensitivity to electrolyte levels. Such sensitivity means that the size and location of the physically stable composition range and the tolerable viscosity range vary greatly depending on the amount of dissolved electrolyte. The use of large amounts, especially of more soluble builders such as NTA, usually makes the liquid unstable and prone to precipitation or phase separation. For these reasons, it is an object of the present invention to provide a composition of the aforementioned type, which is less sensitive to electrolyte substances and whose viscosity is acceptable even when larger amounts of such substances are used. be. Optionally replacing a portion of conventional anionic surfactants with relatively small amounts of certain fatty alcohol polyglycol ether-derived anionic surfactants improves the rheological sensitivity to electrolytes, especially builders and simple electrolyte salts. was found to decrease. Therefore, the present invention includes a synthetic anionic cleansing substance and an electrolyte salt, and has the following formula R-(OC o H 2o ) x -O(CH 2 ) y -COOM [wherein R represents 8 to 20 carbon atoms] or an aliphatic-aromatic hydrocarbon group having from 4 to 20 carbon atoms in the aliphatic part;
n is a number from 2 to 3, x is a number from 1 to 16, y is a number from 0 to 2, and M is a cation] Fatty alcohol polyalkylene oxide carboxylic acid salt or a mixture of these salts from 0.5 to
Provided is a liquid detergent composition containing an aqueous builder having a particulate matter suspending action, characterized in that the composition contains 10% by weight. The alkyl polyalkylene oxide carboxylic acid salt of the present invention is characterized by being represented by the following formula: R-(OC o H 2o ) x -O(CH 2 ) y -COOM. In the above formula R is an aliphatic hydrocarbon having 8 to 20 carbon atoms, or can also be an aliphatic-aromatic hydrocarbon having 4 to 20 carbon atoms in the aliphatic portion. R usually consists of a mixture of linear or branched, saturated or unsaturated aliphatic hydrocarbon groups of various lengths, preferably a linear saturated aliphatic hydrocarbon having 1 to 14 carbon atoms. The polyalkylene oxide moiety (OC o H 2o ) x is preferably an ethylene oxide unit (n=
2), but also propylene oxide or a mixture of propylene oxide and ethylene oxide (2<n3). The number (x) of ethylene and/or propylene oxide units is from 1 to 16, in particular from 1 to 12. The alkylene oxide moiety preferably contains 2 to 5 ethylene oxide units. The carboxylate moiety ((CH 2 ) y -COOM) is preferably free of alkyl chains (y=0), but may contain short alkyl chains such as methylene and ethylene. M is a cation selected from hydrogen, sodium, potassium, ammonium, mono-, di- and triethanolammonium;
Preferred are alkali metal cations. The detergent compositions of the present invention contain a fatty alcohol polyalkylene oxide carboxylic acid salt or a mixture of these salts in an amount of 0.5 to 10% to optionally replace a portion of the synthetic anionic detergent agent. The preferred amount depends on the rheology of the carboxylate compound-free composition and the desired rheology.
Typically, best results are obtained when 2 to 5% by weight of fatty alcohol polyalkylene oxide carboxylic acid salt is used in place of approximately the same amount of synthetic anionic detergent agent. The present invention is particularly applicable to aqueous liquid built compositions based on synthetic anionic detergent agents and electrolyte salts, where suitable synthetic anionic detergent agents include alkylaryl sulfonate type, alkyl Examples include known anionic detergents such as - and alkyl ether sulfate types, alkane and alkenesulfonate types, and the like.
Many other examples include Detergents and Surface-Active Agents by Schwartz, Perry.
Volume 1, 1958. Alkylarylsulfonates, preferably those in which the alkyl chain has 10 to 18 carbon atoms, such as n-dodecylbenzenesulfonate, tetrapropylenebenzenesulfonate, n-pentadecylbenzenesulfonate, and aliphatic Linear C 12 − groups such as those obtained from decomposed wax polymers
C 15 alkylbenzenesulfonic hydrochloric acid, both of which are used in the form of sodium or potassium salts. The total amount of synthetic anionic cleansing agents is 6-12% by weight of the total composition. The main cleansing active ingredients are the anionic substances mentioned above, but other cleansing active substances, especially non-ionic cleansing active substances, may also be used in small amounts. Non-ionic detergents are usually
Consists of a hydrophobic moiety reacted with alkylene oxide. Suitable are primary or secondary, linear or branched C8 - C18 alcohols fused with 1 to 30 mol of alkylene oxide; mono- or dialkylphenols having ~18 carbon atoms, C10 - C18 fatty acid mono- or dialkylolamides condensed with 1 to 30 moles of alkylene oxide, block copolymers of different or identical alkylene oxides, etc. Can be mentioned. The alkylene oxide is usually ethylene oxide, but propylene oxide or a mixture of ethylene oxide and propylene oxide may also be used. Other suitable examples are M.
Listed in "Nonionic Surfactants" by M. Schick. The amount of nonionic detersive agent that may be incorporated into the compositions of the invention is up to 5%, but must be less than the amount of synthetic anionic detersive agent. The electrolyte used in the present invention is one that causes partial salting out of the cleaning agent. The compositions according to the invention may normally contain from 1 to 60% by weight, preferably from 3 to 50% by weight, particularly preferably from 5 to 30% by weight of electrolyte. Representative examples include builder salts such as alkali metal ortho- and pyrophosphates, alkali metal ammonium tripolyphosphates such as sodium tripolyphosphate, alkali metal citrates,
Examples include alkali metal salts of nitrilotriacetic acid and alkali metal salts of carboxymethyloxysuccinic acid. Suitable electrolytes also include buffers such as alkanolamines, especially triethanolamine, alkali metal carboxylates, alkali metal borates, alkali metal silicates, and the like. The compositions of the invention furthermore contain all the ingredients normally included in products of this type, such as alkali metal sulphites to increase the detergency, enzymes alone or polyalcohols or alkanolamines used together with e.g. borax. enzymes, fluorophores, other builders such as zeolites, in combination with enzyme stabilizers such as
abrasives such as calcite, soil suspending agents, anti-redeposition agents, hydrotopes, corrosion inhibitors, foam increasing or reducing agents, emulsifying agents.
agents), fragrances, colorants, and bleaching agents, optionally in combination with bleaching agent precursors. Products of the invention may be manufactured using conventional techniques. In this case the product is post-stirring
It has been found advantageous to shear at the end of the manufacturing process until a maximum stable viscosity is obtained, such as by applying a viscosity or passing through a desintegrator or similar high-shear exerting equipment.
Products treated in this way do not suffer from viscosity effects when subjected to further shear during pumping and bottling operations. Next, the present invention will be explained with reference to Examples. All percentages shown herein are percentages by weight based on the final composition. EXAMPLES According to the formulations listed in Table 1, compositions with high physical stability and significantly higher tolerance to high electrolyte levels were prepared.

【表】
残部水
【table】
remaining water

【表】【table】

Claims (1)

【特許請求の範囲】 1 アルキル鎖が10〜18個の炭素原子を有するア
ルキルアリールスルホン酸塩の合成陰イオン系洗
浄作用物質6〜12重量%と電解質塩1〜60重量%
を含む、不溶ビルダー及び/又は補助粒状物質を
懸濁し得る水性ビルダー入り液体洗剤組成物であ
つて、次式 R−(OCoH2ox−O(CH2y−COOM [式中Rは8〜20個の炭素原子を有する脂肪族
炭化水素基、又は脂肪族部分に4〜20個の炭素原
子を有する脂肪族−芳香族炭化水素基を表わし、
nは2から3までの数、xは1から16までの数、
yは0から2までの数であり、Mは陽イオンを表
わす] で示される脂肪アルコールポリアルキレンオキサ
イドカルボン酸塩又は該塩の混合物を0.5〜10重
量%含むことを特徴とする該組成物。 2 前記Rが1〜14個の炭素原子をもつ直鎖飽和
炭化水素基である特許請求の範囲第1項に記載の
組成物。 3 nが2である特許請求の範囲第1項又は第2
項に記載の組成物。 4 xが2から5までの数である特許請求の範囲
第1項から第3項のいずれかに記載の組成物。 5 yが0である特許請求の範囲第1項から第4
項のいずれかに記載の組成物。 6 Mがアルカリ金属イオンである特許請求の範
囲第1項から第5項のいずれかに記載の組成物。 7 2〜5重量%の脂肪アルコールポリアルキレ
ンオキサイドカルボン酸塩を含む特許請求の範囲
第1項から第6項のいずれかに記載の組成物。 8 5重量%までの非イオン系洗浄作用物質を更
に含み、この非イオン系洗浄作用物質の量が合成
陰イオン系洗浄作用物質の量よりも少ない特許請
求の範囲第1項から第7項のいずれかに記載の組
成物。
[Scope of Claims] 1 Synthetic anionic detersive agent of alkylaryl sulfonate having 10 to 18 carbon atoms in the alkyl chain 6 to 12% by weight and 1 to 60% by weight of electrolyte salt
An aqueous built liquid detergent composition capable of suspending an insoluble builder and/or auxiliary particulate material comprising: R-(OC o H 2o ) x -O(CH 2 ) y -COOM represents an aliphatic hydrocarbon group having 8 to 20 carbon atoms, or an aliphatic-aromatic hydrocarbon group having 4 to 20 carbon atoms in the aliphatic part;
n is a number from 2 to 3, x is a number from 1 to 16,
y is a number from 0 to 2, and M represents a cation] The composition is characterized in that it contains 0.5 to 10% by weight of a fatty alcohol polyalkylene oxide carboxylic acid salt or a mixture of these salts. 2. The composition of claim 1, wherein R is a straight chain saturated hydrocarbon group having 1 to 14 carbon atoms. 3 Claim 1 or 2 in which n is 2
The composition described in Section. 4. A composition according to any one of claims 1 to 3, wherein x is a number from 2 to 5. 5 Claims 1 to 4 in which y is 0
The composition according to any of paragraphs. 6. The composition according to any one of claims 1 to 5, wherein 6M is an alkali metal ion. 7. A composition according to any one of claims 1 to 6, comprising 2 to 5% by weight of fatty alcohol polyalkylene oxide carboxylate. 8. Claims 1 to 7 further comprising up to 5% by weight of a nonionic cleansing agent, the amount of nonionic cleansing agent being less than the amount of the synthetic anionic cleansing agent. The composition according to any one of the above.
JP60226672A 1984-10-12 1985-10-11 Liquid detergent composition Granted JPS6197395A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8425785 1984-10-12
GB848425785A GB8425785D0 (en) 1984-10-12 1984-10-12 Liquid detergent compositions

Publications (2)

Publication Number Publication Date
JPS6197395A JPS6197395A (en) 1986-05-15
JPH0357958B2 true JPH0357958B2 (en) 1991-09-03

Family

ID=10568081

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Application Number Title Priority Date Filing Date
JP60226672A Granted JPS6197395A (en) 1984-10-12 1985-10-11 Liquid detergent composition

Country Status (9)

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EP (1) EP0178006B1 (en)
JP (1) JPS6197395A (en)
AT (1) ATE56470T1 (en)
AU (1) AU579191B2 (en)
BR (1) BR8505035A (en)
CA (1) CA1232817A (en)
DE (1) DE3579658D1 (en)
GB (1) GB8425785D0 (en)
ZA (1) ZA857798B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4797225A (en) * 1986-09-08 1989-01-10 Colgate-Palmolive Company Nonaqueous liquid nonionic laundry detergent composition containing an alkali metal dithionite or sulfite reduction bleaching agent and method of use
DE3905938A1 (en) * 1989-02-25 1990-08-30 Huels Chemische Werke Ag DETERGENT COMPOSITIONS WITH INCREASED VISCOSITY
WO1995023202A1 (en) * 1994-02-23 1995-08-31 Ecolab Inc. Alkaline cleaners based on alcohol ethoxy carboxylates
US7037884B2 (en) 1994-02-23 2006-05-02 Ecolab Inc. Alkaline cleaners based on alcohol ethoxy carboxylates
NL9401510A (en) * 1994-09-16 1996-05-01 Chem Y Surfactant composition, surfactant concentrate in liquid form, and aqueous bleaching agent having increased viscosity and cleaning activity
TW294720B (en) * 1994-09-30 1997-01-01 Unilever Nv
DE19852973C1 (en) * 1998-11-17 2000-07-20 Cognis Deutschland Gmbh Production of low-viscosity aqueous detergent preparations
CN104159562B (en) * 2012-03-02 2016-12-28 花王株式会社 Composition of skin cleanser
MY167793A (en) * 2012-03-02 2018-09-26 Kao Corp Skin cleanser composition
JP6121098B2 (en) * 2012-03-07 2017-04-26 花王株式会社 Skin cleanser composition
WO2018127390A1 (en) * 2017-01-06 2018-07-12 Unilever N.V. Stain removing composition
CN110914397B (en) 2017-05-10 2021-04-13 荷兰联合利华有限公司 Laundry detergent compositions
CN110621769A (en) * 2017-05-10 2019-12-27 荷兰联合利华有限公司 Laundry detergent compositions

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Publication number Priority date Publication date Assignee Title
FR2014084A1 (en) * 1968-07-31 1970-04-10 Hoechst Ag
DE2206284A1 (en) * 1971-02-16 1972-08-31 Kao Soap Co., Ltd., Tokio Washing agents - contg anionic surface active agent and ether carboxylate
FR2436213A1 (en) * 1978-09-13 1980-04-11 Oreal COMPOSITION FOR TREATING FIBROUS MATERIALS BASED ON CATIONIC AND ANIONIC POLYMERS
US4443362A (en) * 1981-06-29 1984-04-17 Johnson & Johnson Baby Products Company Detergent compounds and compositions

Also Published As

Publication number Publication date
GB8425785D0 (en) 1984-11-21
EP0178006A2 (en) 1986-04-16
ZA857798B (en) 1987-06-24
ATE56470T1 (en) 1990-09-15
BR8505035A (en) 1986-07-29
AU579191B2 (en) 1988-11-17
AU4834485A (en) 1986-04-17
EP0178006A3 (en) 1988-07-20
DE3579658D1 (en) 1990-10-18
EP0178006B1 (en) 1990-09-12
JPS6197395A (en) 1986-05-15
CA1232817A (en) 1988-02-16

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