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JPS62277498A - Liquid detergent composition - Google Patents

Liquid detergent composition

Info

Publication number
JPS62277498A
JPS62277498A JP12043586A JP12043586A JPS62277498A JP S62277498 A JPS62277498 A JP S62277498A JP 12043586 A JP12043586 A JP 12043586A JP 12043586 A JP12043586 A JP 12043586A JP S62277498 A JPS62277498 A JP S62277498A
Authority
JP
Japan
Prior art keywords
water
weight
acid
carboxylic acid
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.)
Pending
Application number
JP12043586A
Other languages
Japanese (ja)
Inventor
孝一 松田
中栄 篤男
守康 村田
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP12043586A priority Critical patent/JPS62277498A/en
Publication of JPS62277498A publication Critical patent/JPS62277498A/en
Pending legal-status Critical Current

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  • 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】 3、発明の詳細な説明 〔産業上の利用分野〕 本発明は相安定性の優れた液体洗浄剤組成物に関する。[Detailed description of the invention] 3. Detailed description of the invention [Industrial application field] The present invention relates to a liquid detergent composition with excellent phase stability.

〔従来の技術〕[Conventional technology]

液体洗剤は、一般に、粉末洗剤に比べ水への溶解性に優
れ、低温度から高温度に到るまで広い温度範囲で使用で
きる反面、洗浄力が劣る、並びに溶液の安定性、即ち、
低温における沈澱、ゲル化、固結、高温における分離、
沈澱が生じ易いという問題があった。特に、通常の水和
性有機溶剤を含む系では高温での安定性が不充分であっ
た。
Liquid detergents generally have better solubility in water than powder detergents and can be used in a wide temperature range from low to high temperatures, but on the other hand, they have poor cleaning power and poor solution stability, i.e.
precipitation, gelation, and consolidation at low temperatures; separation at high temperatures;
There was a problem that precipitation was likely to occur. In particular, systems containing conventional hydratable organic solvents had insufficient stability at high temperatures.

これらの問題を解決するため多くの研究がなされている
。例えば、特開昭52−82909号公報は陰イオン活
性剤及び/又は非イオン活性剤、高級脂肪酸塩、低級ア
ルキルベンゼンスルホン酸塩、無機質ビルグー、多価カ
ルボン酸塩を含有する洗浄力、低高温安定性の優れた液
体洗剤組成物に関する。
Many studies have been conducted to solve these problems. For example, JP-A-52-82909 discloses cleaning power containing anionic activators and/or nonionic activators, higher fatty acid salts, lower alkylbenzene sulfonates, inorganic building blocks, polyvalent carboxylic acid salts, and low high temperature stability. The present invention relates to a liquid detergent composition with excellent properties.

特開昭58−65795号公報は非イオン活性剤および
/または陰イオン活性剤、特定のCaイオン捕捉能を有
するポリアクリル酸水溶性塩および低級アルキルベンゼ
ンスルホン酸系の可溶化剤を含有する水溶性ポリアクリ
ル酸塩の保存安定性を改良した、特に泥汚れに対して優
れた洗浄力を有する液体洗剤組成物に関する。
JP-A-58-65795 discloses a water-soluble activator containing a nonionic activator and/or anionic activator, a polyacrylic acid water-soluble salt having a specific Ca ion-trapping ability, and a lower alkylbenzenesulfonic acid-based solubilizer. This invention relates to a liquid detergent composition that has improved storage stability of polyacrylate and has excellent cleaning power, especially against mud stains.

又、特開昭60−141798号公報は、陰イオン活性
剤、ポリカルボン酸重合体および可溶化剤を含有し、組
成物のpHが7〜14に調整された保存安定性の良好な
液体洗剤組成物に関する。
Moreover, JP-A-60-141798 discloses a liquid detergent with good storage stability, which contains an anionic activator, a polycarboxylic acid polymer, and a solubilizer, and whose pH is adjusted to 7 to 14. Regarding the composition.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

一方、液体洗剤の洗浄力を増強するために水溶性ポリア
クリル酸塩などの高分子ビルダーを配合した場合、保存
安定性が悪化する傾向があり、その解決のために特定の
可溶化剤を必要とするが、それでもなお保存安定性は必
ずしも十分でなかった。この悪化傾向は濃縮化のために
界面活性剤濃度を高くした時、あるいは洗浄力増強のた
めに陰イオン活性剤と非イオン活性剤を併用した時に著
しくなるという問題があった。
On the other hand, when a polymer builder such as water-soluble polyacrylate is added to enhance the cleaning power of liquid detergent, storage stability tends to deteriorate, and a specific solubilizer is required to solve this problem. However, the storage stability was still not necessarily sufficient. This deterioration tendency becomes more pronounced when the surfactant concentration is increased for concentration, or when an anionic surfactant and a nonionic surfactant are used together to enhance detergency.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らは、鋭意検討の結果、特定の重合体を用いる
ことにより前記問題点を悉く解決できることを見い出し
本発明を完成した。
As a result of extensive studies, the present inventors have discovered that all of the above problems can be solved by using a specific polymer, and have completed the present invention.

即ち、本発明は1、 fa)陰イオン活性剤及び(1))非イオン活性剤を(
a)/(b)=3/1〜1/3の重量比で且つ(a) 
+ (bl =15〜50重量%、 (c)平均分子量3000以下の、炭素数6〜18を有
する有機メルカプタンをテロゲンとするα、β不飽和カ
ルボン酸の重合体の水溶性塩又はα。
That is, the present invention comprises (1) fa) an anionic activator and (1) a nonionic activator (
a)/(b) = 3/1 to 1/3 weight ratio, and (a)
+ (bl = 15 to 50% by weight, (c) A water-soluble salt or α of a polymer of α, β unsaturated carboxylic acid having an average molecular weight of 3000 or less and using an organic mercaptan having 6 to 18 carbon atoms as a telogen.

β不飽和カルボン酸と共重合可能なビニル単量体との共
重合体の水溶性塩を0.1〜10重量%、及び(di可
溶化剤を1〜10重量% 含有し、相安定性の優れた液体洗浄剤組成物を提供する
ものである。
Contains 0.1 to 10% by weight of a water-soluble salt of a copolymer of a β-unsaturated carboxylic acid and a copolymerizable vinyl monomer, and 1 to 10% by weight of a (di-solubilizing agent) to provide phase stability. The present invention provides an excellent liquid cleaning composition.

本発明の(al成分である陰イオン性界面活性剤として
は下記(1)〜(8)から選択される1種以上を使用で
きる。そのうち特に好ましいのは(1)、(2)、(3
)、(4)及び(5)である。
As the anionic surfactant (al component) of the present invention, one or more selected from the following (1) to (8) can be used. Particularly preferred among them are (1), (2), and (3).
), (4) and (5).

(1)平均炭素数10〜16のアルキル基を有する直鎖
又は分岐鎖アルキルベンゼンスルホン酸塩。
(1) Straight chain or branched chain alkylbenzene sulfonate having an alkyl group having an average carbon number of 10 to 16.

(2)平均炭素数10〜20の直鎖又は分岐鎖のアルキ
ル基又はアルケニル基を有し、1分子内に平均0.5〜
8モルのエチレンオキサイド或いはプロピレンオキサイ
ド或いはブチレンオキサイド或いはエチレンオキサイド
/プロピレンオキサイド或いはエチレンオキサイド/ブ
チレンオキサイドを付加したアルキル又はアルケニルエ
ーテル硫酸塩。
(2) Contains a linear or branched alkyl group or alkenyl group with an average of 10 to 20 carbon atoms, with an average of 0.5 to 20 carbon atoms per molecule.
Alkyl or alkenyl ether sulfate with 8 moles of ethylene oxide or propylene oxide or butylene oxide or ethylene oxide/propylene oxide or ethylene oxide/butylene oxide.

(3)  平均炭素数10乃至20のアルキル基又はア
ルケニル基を有するアルキル又はアルケニル硫酸塩。
(3) An alkyl or alkenyl sulfate having an alkyl or alkenyl group having an average carbon number of 10 to 20.

(4)平均10〜20の炭素原子を1分子中に有するオ
レフィンスルホン酸塩。
(4) Olefin sulfonate having an average of 10 to 20 carbon atoms in one molecule.

(5)平均10〜20の炭素原子を1分子中に有するア
ルカンスルホン酸塩。
(5) Alkanesulfonate having an average of 10 to 20 carbon atoms in one molecule.

(6)平均炭素数10〜20のアルキル基又はアルケニ
ル基を有し、1分子中に平均0.5〜8モルのエチレン
オキサイド或いはプロピレンオキサイド或いはブチレン
オキサイド或いはエチレンオキサイド/プロピレンオキ
サイド、エチレンオキサイド/ブチレンオキサイドを付
加したアルキル又はアルケニルエーテルカルボン酸塩。
(6) Having an alkyl group or alkenyl group with an average carbon number of 10 to 20, and an average of 0.5 to 8 moles per molecule of ethylene oxide, propylene oxide, butylene oxide, ethylene oxide/propylene oxide, ethylene oxide/butylene Oxide-added alkyl or alkenyl ether carboxylate.

(7)下記の式で表わされるα−スルホ脂肪酸塩又はエ
ステル R−ClIC0□Y O3Z 〔式中Yは炭素数1〜3のアルキル基又は対イオン、Z
は対イオンである。Rは炭素数10〜20のアルキル基
又はアルケニル基を表わす。〕ここで陰イオン性界面活
性剤の対イオンとしてはナトリウム、カリウム等のアル
カリ金属イオン、カルシウム、マグネシウム等のアルカ
リ土類金属イオン、アンモニウムイオン、炭素数2又は
3のアルカノール基を1〜3個有するアルカノールアミ
ン(例えばモノエタノールアミン、ジェタノールアミン
、トリエタノールアミン、トリイソプロパツールアミン
など)を挙げることができる。
(7) α-sulfo fatty acid salt or ester R-ClIC0□Y O3Z represented by the following formula [wherein Y is an alkyl group having 1 to 3 carbon atoms or a counter ion, Z
is the counterion. R represents an alkyl group or alkenyl group having 10 to 20 carbon atoms. ] Here, the counter ions of the anionic surfactant include alkali metal ions such as sodium and potassium, alkaline earth metal ions such as calcium and magnesium, ammonium ions, and 1 to 3 alkanol groups having 2 or 3 carbon atoms. Examples include alkanolamines (eg, monoethanolamine, jetanolamine, triethanolamine, triisopropanolamine, etc.).

本発明の(bl成分である非イオン性界面活性剤として
は下記(11〜(8)から選択される1種以上を使用で
きる。そのうち特に好ましいのは(1)、(2)及び(
5)である。
As the nonionic surfactant which is the (bl component) of the present invention, one or more selected from the following (11 to (8)) can be used. Particularly preferred among them are (1), (2) and (
5).

(1)平均炭素数10〜20のアルキル基又はアルケニ
ル基を存し、1〜20モルのエチレンオキサイドを付加
したポリオキシエチレンアルキル又はアルケニルエーテ
ル。
(1) Polyoxyethylene alkyl or alkenyl ether containing an alkyl group or alkenyl group having an average carbon number of 10 to 20 and to which 1 to 20 moles of ethylene oxide is added.

(2)平均炭素数6〜12のアルキル基を有し、1〜2
0モルのエチレンオキサイドを付加したポリオキシエチ
レンアルキルフェニルエーテル。
(2) having an alkyl group with an average carbon number of 6 to 12, and 1 to 2
Polyoxyethylene alkylphenyl ether with 0 moles of ethylene oxide added.

(3)  平均炭素数10〜20のアルキル基又はアル
ケニル基を有し、1〜20モルのプロピレンオキサイド
を付加したポリオキシプロピレンアルキル又はアルケニ
ルエーテル。
(3) Polyoxypropylene alkyl or alkenyl ether having an alkyl group or alkenyl group having an average carbon number of 10 to 20 and to which 1 to 20 mol of propylene oxide is added.

(4)平均炭素数10〜20のアルキル基又はアルケニ
ル基を有し1〜20モルのブチレンオキサイドを付加し
たポリオキシブチレンアルキル又はアルケニルエーテル
(4) Polyoxybutylene alkyl or alkenyl ether having an alkyl group or alkenyl group having an average carbon number of 10 to 20 and added with 1 to 20 moles of butylene oxide.

(5)平均炭素数10〜20のアルキル基又はアルケニ
ル基を有し、総和で1〜30モルのエチレンオキサイド
とプロピレンオキサイド或いはエチレンオキサイドとブ
チレンオキサイドを付加した非イオン性活性剤。
(5) A nonionic activator having an alkyl group or alkenyl group having an average carbon number of 10 to 20 and to which a total of 1 to 30 moles of ethylene oxide and propylene oxide or ethylene oxide and butylene oxide are added.

(6)下記の一般式で表わされる高級脂肪酸アルカノー
ルアミド又はそのアルキレンオキサイド付加物 R′、2 R′1□ c式中R°1.は炭素数10〜20のアルキル基、又は
アルケニル基であり、R°1□は11又はC113であ
り、i、は1〜3の整数、ll13は0〜3の整数であ
る。〕 (7)平均炭素数10〜20の脂肪酸と蔗糖から成る蔗
糖脂肪酸エステル。
(6) Higher fatty acid alkanolamide or its alkylene oxide adduct R', 2 R'1□ c in the formula R°1. is an alkyl group or alkenyl group having 10 to 20 carbon atoms, R°1□ is 11 or C113, i is an integer of 1 to 3, and ll13 is an integer of 0 to 3. ] (7) Sucrose fatty acid ester consisting of a fatty acid with an average carbon number of 10 to 20 and sucrose.

(8)平均炭素数10〜20の脂肪酸とグリセリンから
成る脂肪酸グリセリンモノエステル。
(8) Fatty acid glycerin monoester consisting of a fatty acid having an average carbon number of 10 to 20 and glycerin.

(al成分と(b)成分は重量比で3/1〜1/3、好
ましくは2/1〜1/2の割合で、総量で15〜50重
量%(以下%と略す)、好ましくは25〜45%配合さ
れる。この範囲内で洗浄力および相安定性がともに優れ
た組成物を得ることができる。
(Al component and component (b) are in a weight ratio of 3/1 to 1/3, preferably 2/1 to 1/2, and the total amount is 15 to 50% by weight (hereinafter abbreviated as %), preferably 25% by weight. ~45%. Within this range, a composition with excellent detergency and phase stability can be obtained.

本発明の(C)成分である重合体あるいは共重合体の水
溶性塩は、例えば特開昭59−91184号公報、米国
特許第3922230号明細書で金属イオン封鎖剤とし
て知られているものである。
The water-soluble salt of the polymer or copolymer which is the component (C) of the present invention is known as a sequestering agent as described in, for example, JP-A-59-91184 and US Pat. No. 3,922,230. be.

ここで、テロゲンとして用いられる有機メルカプタンと
しては、例えばヘキシル−、オクチル−、デシル−、ド
デシル−、テトラデシル−。
Here, examples of organic mercaptans used as telogens include hexyl, octyl, decyl, dodecyl, and tetradecyl.

ヘキサデシル−、オクタデシル−等のメルカプタン、2
−ヒドロキシ−ドデシルメルカプタン、ドデシルヘンゼ
ンオールなどが挙げられる。
Mercaptans such as hexadecyl and octadecyl, 2
-Hydroxy-dodecylmercaptan, dodecylhenzenol, and the like.

本発明で用いるα、β不飽和カルボン酸は次の一般式(
[)で表わされる。
The α,β-unsaturated carboxylic acid used in the present invention has the following general formula (
Represented by [).

Z C=C(1) Y  C00)I 〔式中、X、Y、Zはそれぞれ−IL −C11,、−
COOIL −011又は−C1lzCOOIIを示す
。] 一般式(1)で表わされるα、β不飽和カルボン酸の重
合体の塩としては、例えばアクリル酸、メタクリル酸、
2−ヒドロキシアクリル酸、フマル酸、マレイン酸、イ
タコン酸、アコニット酸、シトラコン酸等の塩が挙げら
れる。
Z C=C(1) Y C00)I [wherein, X, Y, and Z are each -IL -C11,, -
Indicates COOIL-011 or -C1lzCOOII. ] Examples of the salt of the α,β-unsaturated carboxylic acid polymer represented by the general formula (1) include acrylic acid, methacrylic acid,
Examples include salts of 2-hydroxyacrylic acid, fumaric acid, maleic acid, itaconic acid, aconitic acid, citraconic acid, and the like.

さらにエチレン、スチレン、ブタジェン、イソブチレン
、ジイソブチレン、メチルビニルエーテル、酢酸ビニル
、ビニルピロリドン、アクリルニトリル等のビニル系モ
ノマーをコモノマーとして用いることもできる。
Furthermore, vinyl monomers such as ethylene, styrene, butadiene, isobutylene, diisobutylene, methyl vinyl ether, vinyl acetate, vinylpyrrolidone, and acrylonitrile can also be used as comonomers.

本発明において重合体又は共重合体の水溶性塩を構成す
るアルカリ金属としてはナトリウム、カリウム、リチウ
ムが挙げられ、アミンとしてはアンモニア、モノ−、ジ
ー又はトリーエタノールアミン、モルホリン等が挙げら
れ、これらの塩は当然ながら部分塩であっても良い。
In the present invention, the alkali metals constituting the water-soluble salt of the polymer or copolymer include sodium, potassium, and lithium, and the amines include ammonia, mono-, di-, or tri-ethanolamine, morpholine, etc. Naturally, the salt may be partial salt.

これら重合体又は共重合体の水溶性塩の平均分子量は溶
解性の面から、3000以下であり、望ましくは500
〜2000である。さらに重合部分が分子全体の95%
以下、特に90%未満である事が望ましい。
The average molecular weight of the water-soluble salt of these polymers or copolymers is 3000 or less, preferably 5000 or less, from the viewpoint of solubility.
~2000. Furthermore, the polymerized portion accounts for 95% of the entire molecule.
Below, it is particularly desirable that it be less than 90%.

(c)成分の配合量は0.1〜10%、好ましくは0.
5〜5%である。0.1%未満では相安定性効果がなく
、また10%を越えると相安定性は悪化してく る。
The blending amount of component (c) is 0.1 to 10%, preferably 0.1% to 10%.
It is 5-5%. If it is less than 0.1%, there will be no phase stability effect, and if it exceeds 10%, the phase stability will deteriorate.

本発明では相安定化のために(cl)成分である可溶化
剤を必要とする。
The present invention requires a solubilizer as a (cl) component for phase stabilization.

可溶化剤としては、エタノールのような低級アルコール
、ベンゼンスルホン酸塩、p−トルエンスルホン酸塩の
ような低級アルキルベンゼンスルホン酸塩、プロピレン
グリコールのようなグリコール類、アセチルベンゼンス
ルホン酸塩、アセトアミド類、ピリジンジカルボン酸ア
ミド類、安息香酸塩又は尿素等の可溶化剤が挙げられる
が、特に限定されるものではない。
Examples of solubilizers include lower alcohols such as ethanol, lower alkylbenzenesulfonates such as benzenesulfonates and p-toluenesulfonates, glycols such as propylene glycol, acetylbenzenesulfonates, acetamides, Solubilizing agents such as pyridine dicarboxylic acid amides, benzoates, and urea may be mentioned, but are not particularly limited.

可溶化剤は通常1〜10%の範囲で用いる。1%未満で
は低温における粘度低下作用、固結防止作用を充分発蓮
できず、10%を越えると高温において沈澱を生ずる傾
向がある。特にエタノールは液体洗剤の長期保存に際し
発生する菌の防止にも役立つので好ましい。エタノール
は3〜7%の範囲で使用するのがよい。
The solubilizer is usually used in an amount of 1 to 10%. If it is less than 1%, the viscosity-reducing effect and anti-caking effect at low temperatures cannot be fully exerted, and if it exceeds 10%, precipitation tends to occur at high temperatures. In particular, ethanol is preferable because it is useful for preventing bacteria generated during long-term storage of liquid detergents. Ethanol is preferably used in a range of 3 to 7%.

この他任意成分として、プロテアーゼ、アミラーゼ、リ
パーゼ、セルラーゼ等の酵素、及び塩化カルシウム等の
酵素安定化剤、螢光染料、香料等も、通常の範囲内で配
合できる。
In addition, as optional components, enzymes such as protease, amylase, lipase, and cellulase, enzyme stabilizers such as calcium chloride, fluorescent dyes, fragrances, and the like may also be included within the usual range.

〔実施例〕〔Example〕

以下実施例により本発明を更に詳しく説明するが、本発
明はこれら実施例に限定されるものではない。
The present invention will be explained in more detail below with reference to Examples, but the present invention is not limited to these Examples.

実施例1 以下のサンプルを調製し、その評価結果を表−1に示し
た。
Example 1 The following samples were prepared and the evaluation results are shown in Table-1.

エタノール               5水 道 
水           バランス評価は次の基準によ
り行った。
Ethanol 5 Water
Water balance evaluation was performed based on the following criteria.

(11相安定性 各サンプルを調製後、直径4cm高さ1oc111のス
クリュー管に入れ、−5℃、常温、40’Cに1ケ月保
存し、判定した。
(11 Phase Stability After each sample was prepared, it was placed in a screw tube with a diameter of 4 cm and a height of 1 oc 111, and was stored at -5°C, room temperature, and 40'C for 1 month, and then evaluated.

○:均−透明液体 ×:沈澱、濁り、分離を生じた。○: Uniform-transparent liquid ×: Precipitation, turbidity, and separation occurred.

(2)洗浄力試験 洗剤水溶液1βに10cm X 10cmの綿の泥汚れ
汚染布9 (人工汚染布)を5枚入れ、ターボトメ−タ
ーにて100rpa+で次の条件で洗浄した。
(2) Detergent power test Five 10 cm x 10 cm mud-stained cotton cloths 9 (artificially contaminated cloths) were placed in detergent aqueous solution 1β and washed with a turbotometer at 100 rpa+ under the following conditions.

洗浄条件は次の通り。The washing conditions are as follows.

(洗浄条件) 洗浄時間  1o分 洗浄濃度 0.133% 水の硬度  4°Dl+ 水      温    20”C ススギ     水道水にて5分間 洗浄力は汚染前の原布及び洗浄前後の汚染布の反射率を
自記色彩計(島津製作所製)にで測定し次式によって洗
浄率(%)を求めた。
(Washing conditions) Washing time: 10 minutes Washing concentration: 0.133% Water hardness: 4°Dl + Water temperature: 20”C Sugi Sugi 5 minutes with tap water The cleaning power is based on the reflectance of the original cloth before contamination and the contaminated cloth before and after cleaning. It was measured with a self-recording colorimeter (manufactured by Shimadzu Corporation), and the cleaning rate (%) was determined using the following formula.

(表には5枚の測定平均値を示す)。(The table shows the average value measured for 5 sheets).

〕 孝)泥汚れ汚染布(人工汚染布) 鹿沼園芸用赤玉土を120 ’C±5℃で4hr乾燥後
粉砕、150Mesh (100μo+)バスのものを
120℃±5℃2hr乾燥後、+150gを10001
のパークレンに分散し、金巾# 2023布をこの液に
接触、ブラッシングし、分散液の除去、過剰付着汚れを
脱落させる(特開昭55−26473号)。
] Takashi) Mud soil contaminated cloth (artificially contaminated cloth) Akadama soil for Kanuma gardening was dried at 120'C ± 5℃ for 4 hours, then crushed, 150Mesh (100μo+) Bath stuff was dried at 120℃ ± 5℃ for 2 hours, +150g was pulverized to 10001
The dispersion liquid is removed and excess dirt is removed by contacting and brushing a #2023 gold cloth with the liquid (Japanese Patent Application Laid-open No. 55-26473).

実施例2 各成分の組成を表−2の通りに変え、実施例1と同様に
相安定性、洗浄率を評価した。
Example 2 The composition of each component was changed as shown in Table 2, and the phase stability and cleaning rate were evaluated in the same manner as in Example 1.

結果を表−2に併せて示す。The results are also shown in Table-2.

Claims (1)

【特許請求の範囲】 (a)陰イオン活性剤及び(b)非イオン活性剤を(a
)/(b)=3/1〜1/3の重量比で且つ(a)+(
b)=15〜50重量%、 (c)平均分子量3000以下の、炭素数6〜18を有
する有機メルカプタンをテロゲンとするα,β不飽和カ
ルボン酸の重合体の水溶性塩又はα,β不飽和カルボン
酸と共重合可能なビニル単量体との共重合体の水溶性塩
を0.1〜10重量%、及び(d)可溶化剤を1〜10
重量% 含有することを特徴とする液体洗浄剤組成物。
[Scope of Claims] (a) an anionic activator and (b) a nonionic activator (a)
)/(b)=3/1 to 1/3 weight ratio and (a)+(
b) = 15 to 50% by weight, (c) a water-soluble salt of a polymer of α,β unsaturated carboxylic acid or an α,β unsaturated carboxylic acid having an average molecular weight of 3000 or less and using an organic mercaptan having 6 to 18 carbon atoms as a telogen; 0.1 to 10% by weight of a water-soluble salt of a copolymer of a saturated carboxylic acid and a copolymerizable vinyl monomer, and (d) 1 to 10% of a solubilizer.
% by weight.
JP12043586A 1986-05-26 1986-05-26 Liquid detergent composition Pending JPS62277498A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12043586A JPS62277498A (en) 1986-05-26 1986-05-26 Liquid detergent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12043586A JPS62277498A (en) 1986-05-26 1986-05-26 Liquid detergent composition

Publications (1)

Publication Number Publication Date
JPS62277498A true JPS62277498A (en) 1987-12-02

Family

ID=14786138

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12043586A Pending JPS62277498A (en) 1986-05-26 1986-05-26 Liquid detergent composition

Country Status (1)

Country Link
JP (1) JPS62277498A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2717183A1 (en) * 1994-03-11 1995-09-15 Hoechst France Water-soluble detergent concentrates for textile treatment
US5489397A (en) * 1994-03-04 1996-02-06 National Starch And Chemical Investment Holding Corporation Aqueous lamellar detergent compositions with hydrophobically terminated hydrophilic polymer
US5599784A (en) * 1994-03-04 1997-02-04 National Starch And Chemical Investment Holding Corporation Aqueous lamellar detergent compositions with hydrophobically capped hydrophilic polymers
US5698511A (en) * 1994-12-05 1997-12-16 Colgate-Palmolive Company Granular detergent compositions containing deflocculating polymers and process for preparing such compositions
US6090762A (en) * 1993-05-07 2000-07-18 Albright & Wilson Uk Limited Aqueous based surfactant compositions
US6177396B1 (en) 1993-05-07 2001-01-23 Albright & Wilson Uk Limited Aqueous based surfactant compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6090762A (en) * 1993-05-07 2000-07-18 Albright & Wilson Uk Limited Aqueous based surfactant compositions
US6177396B1 (en) 1993-05-07 2001-01-23 Albright & Wilson Uk Limited Aqueous based surfactant compositions
US5489397A (en) * 1994-03-04 1996-02-06 National Starch And Chemical Investment Holding Corporation Aqueous lamellar detergent compositions with hydrophobically terminated hydrophilic polymer
US5599784A (en) * 1994-03-04 1997-02-04 National Starch And Chemical Investment Holding Corporation Aqueous lamellar detergent compositions with hydrophobically capped hydrophilic polymers
FR2717183A1 (en) * 1994-03-11 1995-09-15 Hoechst France Water-soluble detergent concentrates for textile treatment
US5698511A (en) * 1994-12-05 1997-12-16 Colgate-Palmolive Company Granular detergent compositions containing deflocculating polymers and process for preparing such compositions

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