JPH11236596A - Aqueous composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an aq. compsn. improved in storage stability and bleaching- cleaning performance by incorporating, into the same, a specific cationic surfactant and a peracid precursor which reacts with hydrogen peroxide in an aq. soln. to form an org. peracid. SOLUTION: This compsn. comprises (A) water, (B) 0.01-60 wt.%, pref. 0.140 wt.%, peracid precursor which reacts with hydrogen peroxide in an aq. soln. to form an org. peracid, and (C) 0.01-60 wt.%. pref. 0.1-40 wt.%, cationic surfactant of the formula (wherein R<1> is an optionally hydroxylated linear or branched 1-22C alkyl, acyl, alkenyl, or alkoxy group or a phenyl or benzyl group optionally substd. by a 1-8C alkyl group; R<2> is a linear or branched 1-8C alkylene group optionally hydroxylated and optionally interrupted by a carbocycle; R<3> to R<5> are each H, an optionally hydroxylated linear or branched 1-18C alkyl, or the like; and X is an anionic group such as a halogen anion group or an alkylsulfate anion group) and is adjusted to a pH of 7-13.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an aqueous composition having an improved stability of a peracid precursor in an aqueous solution. The present invention also relates to a washing method which exhibits excellent bleaching performance and is particularly suitable as a method for removing mold.

[0002]

2. Description of the Related Art Bleaching agents are used not only for stains on clothes, spills, squirrel stains or oil stains, but also for small articles such as tableware and kitchen utensils. In such a case, by immersing in the aqueous solution, dirt and various germs remaining on the surface can be easily removed. In addition, the use of bleaching agents has been studied for mold stains that occur in humid places such as the eyes and walls of bathtubs. However, since mold stains are stubborn stains, a sufficient effect cannot be obtained with an oxygen-based bleach using ordinary hydrogen peroxide. In order to solve these problems, a combination with a peroxide precursor having a stronger bleaching power by reacting with hydrogen peroxide is being studied, but when the peroxide precursor is mixed with the same solution as hydrogen peroxide, Stabilization is difficult because they react with each other. Therefore, a method has been proposed in which the hydrogen peroxide system and the peracid precursor system are separated and mixed at the time of use. However, since the peracid precursor is hydrolyzed in an aqueous solution upon storage, there is a problem that the bleaching performance is reduced during actual use.

An object of the present invention is to provide an aqueous composition capable of securing sufficient bleaching performance even when blended with a bleaching component at the time of use by enhancing the storage stability of a peracid precursor in an aqueous solution. With the goal. Further, the present invention exerts excellent bleaching / cleaning performance by reacting with hydrogen peroxide or a compound which generates hydrogen peroxide in an aqueous solution (hereinafter referred to as "hydrogen peroxide releasing body"), and particularly a method for removing mold. Another object of the present invention is to provide a useful cleaning method.

[0004]

The present invention provides (a) a peracid precursor which reacts with hydrogen peroxide in an aqueous solution to form an organic peracid, and (b) a general formula (1) shown below:

[0005]

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[Wherein, R ¹ is a straight-chain or branched-chain alkyl, acyl, aryl, alkenyl, alkoxy or alkoxy group having 1 to 22 carbon atoms which may be substituted with a hydroxyl group. A phenyl group or a benzyl group which may be substituted with an alkyl group of 8; R ² is a linear or branched alkylene having 1 to 8 carbon atoms which is substituted with a hydroxyl group and which may be interrupted by a carbocyclic ring; A group; R ³ , R ⁴ , R ⁵
Is a hydrogen atom which may be the same or different, and a linear or branched carbon atom having 1 to 1 carbon atoms which may be substituted with a hydroxyl group.
8, an alkyl group, an acyl group, an aryl group, an alkenyl group, an alkoxy group, a phenyl group which may be substituted with an alkyl group having 1 to 8 carbon atoms, and a phenyl group which may be substituted with an alkyl group having 1 to 8 carbon atoms A benzyl group or an alkylene oxide group having an average addition mole number of 1 to 50 and having 1 to 4 carbon atoms, and when R ³ , R ⁴ and R ⁵ are alkylene oxide groups, the added alkylene groups may be the same or different. Often,
The sequence is also arbitrary; X represents an anionic substance such as a halogen anion group or an alkyl sulfate anion group. An aqueous composition containing a cationic surfactant represented by the formula:

[0007]

BEST MODE FOR CARRYING OUT THE INVENTION The peracid precursor (a) used in the present invention is not particularly limited as long as it reacts with hydrogen peroxide in an aqueous solution to form an organic peracid.
As the peracid precursor of the component (a), for example, a compound represented by the general formula (2): R ⁶ —C (＝ O) -L (2) [wherein, R ⁶ may be any of a straight chain or a branched chain] An alkyl group having 4 to 18 carbon atoms, an aryl group, an alkenyl group, an acyl group or the following general formula (3):

[0008]

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Wherein R ⁷ is a hydrogen atom, having 1 to 1 carbon atoms.
Straight or branched chain alkyl group having 8, an alkenyl group, an acyl group; R ⁸ represents a linear or branched alkylene group having 1 to 8 carbon atoms, p is 0 or 1; R ⁹ Represents a linear or branched alkylene group having 1 to 8 carbon atoms or a phenylene group which may be substituted with a linear or branched alkyl group having 1 to 5 carbon atoms;
Represents a straight-chain or branched-chain alkylene group; n is an average number of moles of alkylene oxide added, and represents a number of 0 to 100, and n A's may be the same or different) L represents the following general formulas (4), (5) and (6)
Or (7):

[0010]

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(Wherein, M represents a hydrogen atom, an alkali metal atom or an ammonium group; R ¹⁰ and R ¹¹ represent a linear or branched alkylene group having 1 to 8 carbon atoms). Represents a group. ] Can be mentioned.

[0012] In the general formula (2) representing the peracid precursor of the component (a), the R ⁶ and L, R ⁶ is the formula (3)
Group a group represented by and L is represented by the general formula (4), R ⁶
Is a group represented by the general formula (3) and L is a group represented by the general formula (5), R ⁶ is a group represented by the general formula (3) and L is represented by the general formula (6) It is preferable that the group or R ⁶ be a combination of a group represented by the general formula (3) and L be a group represented by the general formula (7). Among them, those in which R ⁶ is a group represented by the general formula (3) and L is a group represented by the general formula (6) are particularly preferable.

The cationic surfactant of the component (b) used in the present invention has the following general formula (1):

[0014]

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[In the formula, R ¹ is a straight-chain or branched-chain alkyl, acyl, aryl, alkenyl, alkoxy or alkoxy group having 1 to 22 carbon atoms which may be substituted by a hydroxyl group. A phenyl group or a benzyl group which may be substituted with an alkyl group of 8; R ² is a linear or branched alkylene having 1 to 8 carbon atoms which is substituted with a hydroxyl group and which may be interrupted by a carbocyclic ring; A group; R ³ , R ⁴ , R ⁵
Is a hydrogen atom which may be the same or different, and a linear or branched carbon atom having 1 to 1 carbon atoms which may be substituted with a hydroxyl group.
8, an alkyl group, an acyl group, an aryl group, an alkenyl group, an alkoxy group, a phenyl group which may be substituted with an alkyl group having 1 to 8 carbon atoms, and a phenyl group which may be substituted with an alkyl group having 1 to 8 carbon atoms A benzyl group or an alkylene oxide group having an average addition mole number of 1 to 50 and having 1 to 4 carbon atoms, and when R ³ , R ⁴ and R ⁵ are alkylene oxide groups, the added alkylene groups may be the same or different. Often,
The sequence is also arbitrary; X represents an anionic substance such as a halogen anion group or an alkyl sulfate anion group. ].

Examples of the cationic surfactant represented by the general formula (1) include N-lauroylaminopropyl-N, N, N-trimethylammonium chloride and N-lauroylaminopropyl-N, N, N-trimethylammonium chloride.
Octylaminopropyl-N, N-dimethyl-N-benzylammonium chloride, N-palmitylaminopropyl-N, N-dimethyl-N-hydroxyethylammonium chloride, N-octylaminopropyl-N,
N, N-trimethylpropylammonium methyl sulfate and the like can be mentioned.

The content of the components (a) and (b) in the aqueous composition is preferably from 0.01 to 0.01% in order to enhance the stability of the component (a).
The content is 60% by weight, particularly preferably 0.1 to 40% by weight, and the component (b) is preferably 0.01 to 60% by weight, particularly preferably 0.1 to 40% by weight. When components other than the components (a) and (b) are blended in the aqueous composition, the total content of the components (a) and (b) is preferably 80% by weight or less, particularly preferably 60% by weight. %
It is as follows.

The aqueous composition of the present invention preferably further contains a surfactant in order to improve the bleaching detergency. Surfactants include fatty acid soaps, alkyl sulfates, alkylbenzene sulfonates, polyoxyethylene alkyl sulfates, sulfosuccinate diesters, alkyl diphenyl ester disulfonates, alkane sulfonates, alkyl phosphates, α -Anionic surfactants such as olefin sulfates and α-olefin sulfonates; polyoxyethylene alkyl ethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, polyoxyethylene fatty acid esters, fatty acid monoglycerides, alkyl glycosides, amine oxides Nonionic surfactants such as monoalkyltrimethylammonium salt, dialkyldimethylammonium salt, trialkylmethylammonium salt;
Cationic surfactants such as tetraalkylammonium salts and alkyldimethylbenzalkonium salts; alkyldimethylcarbobetaines, alkylamidopropylcarbobetaines, alkylsulfobetaines, alkylhydroxysulfobetaines, alkylamidopropylsulfobetaines, alkylamidopropylhydroxysulfobetaines And the like, and one or more selected from amphoteric surfactants and the like. The amount of the surfactant in the aqueous composition is preferably 0.01 to 30% by weight, particularly preferably 0.05 to 20% by weight.

The aqueous composition of the present invention preferably further contains a water-soluble solvent in order to improve the bleaching detergency and the storage stability. Examples of the water-soluble solvent include ethanol, propanol, propylene glycol, propylene glycol monobutyl ether, propylene glycol monomethyl ether, butyl diglycol, phenoxyethanol, a compound obtained by adding an alkylene oxide to phenol, N-alkylpyrrolidone, and 3-methoxy-3.
One or more selected from -methyl-1-butanol, isoprene glycol and the like can be mentioned. The amount of the water-soluble solvent in the aqueous composition is preferably 0.01 to 40% by weight, particularly preferably 0.1 to 40% by weight.
３０30% by weight.

The aqueous composition of the present invention preferably further contains an organic acid in order to adjust and maintain the pH and to suppress the decomposition of the peracid precursor. Organic acids include citric acid,
One or more selected from succinic acid, malic acid, fumaric acid, tartaric acid, malonic acid and the like can be mentioned. The compounding amount of the organic acid is preferably 0.01 to 30% by weight in the aqueous composition.

The aqueous composition of the present invention preferably further contains a chelating agent for improving the bleaching performance and suppressing the decomposition of the peracid precursor. Examples of the chelating agent include tripolyphosphoric acid, pyrophosphoric acid, orthophosphoric acid, hexametaphosphoric acid, and alkali metal salts thereof, ethylenediaminetetraacetic acid, hydroxyiminodiacetic acid, dihydroxyethylglycine, nitrilotriacetic acid, hydroxyethylenediaminetriacetic acid, diethylenetriaminepentaacetic acid, triethylenetriaminepentaacetic acid, and triethylenephosphoric acid. Ethylene tetramine hexaacetic acid and their alkali metal salts or alkaline earth metal salts, aminotrimethylene phosphonic acid, 1-
N-oxides of hydroxyethylidene-1,1-diphosphonic acid, ethylenediaminetetramethylenephosphonic acid, diethylenetriaminepentamethylenephosphonic acid, aminotrimethylenephosphonic acid and their alkali metal or alkaline earth metal salts, poly-α-hydroxyacrylic acid And one or more selected from alkali metal salts thereof. The amount of the chelating agent is preferably 0.0001 to 10% by weight, particularly preferably 0.001 to 5% by weight, in the aqueous composition.

The aqueous composition of the present invention preferably further contains a water-soluble polymer in order to improve the bleaching detergency. Examples of the water-soluble polymer include, for example,
One or more types selected from those described in page 20, column 10, line 20 to page 7, column 11, line 3 of 209194 can be mentioned, and among them, the following (i) to (iv) are preferable.

(I) guar gum, locust bean gum,
Natural polymers derived from plants such as carrageenan, alginic acid, gum arabic and pectin; (ii) natural polymers derived from microorganisms such as xanthan gum; (iii) oxidation, methylation and carboxymethylation of cellulose, starch, cellulose or starch. A cellulose derivative or a starch derivative processed by a treatment such as hydroxyethylation, hydroxypropylation, or cationization; (iv) a polyacrylic acid homopolymer or a polyacrylic acid derivative that is a copolymer with a monomer copolymerizable with acrylic acid; Crosslinked polyacrylic acid homopolymers or polyacrylic acid derivatives, especially those having a weight average molecular weight of about 2,000.

The amount of the water-soluble polymer in the aqueous composition is preferably from 0.001 to 10% by weight, particularly preferably from 0.01 to 5% by weight.

The aqueous composition of the present invention further contains other components in a range not impairing the object of the present invention, for example, a fragrance, an antibacterial agent, a peracid stabilizer, a pH adjuster, a pigment, a dye and a suspending agent. Can be blended.

The aqueous composition of the present invention preferably has a pH during storage of preferably 1 to prevent decomposition of the peracid precursor.
To 9, and particularly preferably 1.5 to 8.

The aqueous composition of the present invention generates peracid by mixing with hydrogen peroxide and a hydrogen peroxide-releasing substance, and removes stains or performs bleach washing. As a method of using the same, a hard cleaning object such as a fan of a ventilation fan, a range hood, tableware, a kitchen knife, or the like is immersed in an aqueous composition and a cleaning agent in which hydrogen peroxide or a hydrogen peroxide releasing body is dissolved, and left for a while. In addition to the method of washing with water after washing, when used for clothing, the aqueous composition of the present invention is applied directly to stains and Eri Sode stains, along with a detergent containing hydrogen peroxide or a hydrogen peroxide releasing body By washing, an excellent bleaching and washing effect can be obtained. Other objects to be cleaned can also be used as a cleaning booster for such partial contamination. That is, the aqueous composition of the present invention is
It is effective to use the aqueous composition as a cleaning method in which the composition is applied to a soil surface and then treated with a cleaning agent containing hydrogen peroxide or a hydrogen peroxide-releasing substance. In addition, a method of mixing the aqueous composition and hydrogen peroxide or a hydrogen peroxide-releasing substance in a coating container or a spray container immediately before use and applying the mixture to dirt is mentioned. It is suitable for use.

Examples of the hydrogen peroxide emitter include sodium percarbonate, sodium tripolyphosphate / hydrogen peroxide adduct,
Sodium pyrophosphate / hydrogen peroxide adduct, urea / hydrogen peroxide adduct, sodium sulfate / hydrogen peroxide adduct, sodium perborate monohydrate, sodium perborate tetrahydrate, sodium persilicate Examples thereof include sodium peroxide and calcium peroxide. In the present invention, in addition to hydrogen peroxide, sodium percarbonate, sodium perborate monohydrate, and sodium perborate tetrahydrate are preferred.

The pH of the aqueous detergent obtained by mixing the aqueous composition with hydrogen peroxide or a hydrogen peroxide-releasing substance is preferably adjusted to 7 to 13;
It is particularly preferable to adjust to 9 to 13, and more preferably to 9 to 13. Examples of the pH adjusting agent for maintaining the pH in the above range include sodium hydroxide, alkali metal hydroxides such as potassium hydroxide, ammonium hydroxide, amine derivatives such as mono, di or triethanolamine, and sodium carbonate. And alkali metal carbonates such as potassium carbonate, carbonates such as ammonium carbonate, alkali metal silicates such as sodium silicate and potassium silicate, and silicates such as ammonium silicate.

When a discharge vessel such as a trigger spray is used, toluenesulfonic acid, xylenesulfonic acid, cumenesulfonic acid, alkenylsuccinic acid or a mixture thereof is used in order to enhance adhesion to a hard surface and enhance bleaching performance. It is preferable to mix one or more selected from foaming aids such as alkali metal salts. It is preferable to mix the foaming aid in the aqueous composition, and the compounding amount is preferably 0.01 to 20% by weight, particularly preferably 0.05 to 10% by weight.

Further, the aqueous composition of the present invention and the hydrogen peroxide or the hydrogen peroxide-releasing substance are used as separate systems, kept in a non-contact state, and packaged for mixing at the time of use. A two-pack type is preferred. During packaging, other components are chelating agents, pH adjusters, stabilizers such as borate,
Surfactants, foaming aids and oxidation-resistant fragrances may be added to the hydrogen peroxide or hydrogen peroxide emitter as long as they do not decompose hydrogen peroxide. , As long as it does not affect the cationic surfactant in the aqueous composition. When using an aqueous solution of hydrogen peroxide or in order to further improve the detergency, a three-part type in which an alkali agent such as an alkali metal carbonate or an alkali metal silicate is separately packaged may be used. The most preferable one is a two-pack type in which the aqueous composition is packaged and sodium percarbonate or sodium perborate is packaged.

The packaging method is not particularly limited, and can be packaged by appropriately combining bottles and sachets. Materials for bottles and sachets include polyethylene and polypropylene, which are generally used for containers for bleaching detergents.
Examples thereof include polyamide, polyethylene terephthalate, and polyvinylidene chloride. In addition, these plastics can contain a pigment, an antistatic agent, a light-shielding agent, and an ultraviolet absorber as necessary. Bottles and sachets can have a multi-layer structure, and can also be provided with a metal layer such as aluminum. Further, a pinhole, a check valve, or a straw-like pouring means for transferring to another container may be provided.

The amount of the packaged hydrogen peroxide or the hydrogen peroxide releasing substance is preferably 0.01 to 30% by weight, particularly preferably 0.1 to 30% by weight, in terms of hydrogen peroxide in the composition. -20% by weight.

[0034]

EXAMPLE 1 N-lauroylaminopropyl-N, N-dimethylamine (molecular weight 284.) was placed in a 1-liter autoclave equipped with stirring, heating and cooling means, a thermometer and a pressure gauge.
2) 284.2 g, 100 g each of isopropyl alcohol and ion-exchanged water were charged. Then 90 ° C
Heated to methyl chloride (molecular weight 50.5) 50.
5 g was introduced over 1 hour, and the reaction was terminated when the pressure became constant. After cooling, the contents were taken out to obtain N-lauroylaminopropyl-N, N, N-trimethylammonium chloride (cationic activator 1).

Production Examples 2 to 4 According to Production Example 1, N-octylaminopropyl-N,
N, N-trimethylammonium chloride (cationic activator 2), N-palmitylaminopropyl-N, N, N
-Dimethyl-N-hydroxyethylammonium chloride (cationic activator 3) and N-octylaminopropyl-N, N, N-trimethylammonium methyl sulfate (cationic activator 4) were prepared.

Examples 1 to 9 and Comparative Examples 1 to 7 Aqueous compositions (aqueous solutions) having the compositions shown in Table 1 were produced.
As the component (a), the following compounds 1 to 7 were used. Compound 1: sodium octanoyloxybenzenesulfonate Compound 2: sodium dodecanoyloxybenzenesulfonate Compound 3: hexanoyloxybenzenecarboxylic acid

[0037]

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The pH of each composition was adjusted to 5 with sulfuric acid or sodium carbonate. The stability of the peracid precursor in these compositions was tested by the following method. Table 1 shows the results. In addition, the compounding amount in Table 1 is based on the total amount including water, and is represented by% by weight. (Stability of Peracid Precursor) The residual ratio of the peracid precursor when the aqueous composition was left in a room at 40 ° C. for one month was measured.
The residual ratio of the peracid precursor was determined from the ester value obtained by measuring the acid value and saponification value of the aqueous composition.

[0039]

[Table 1]

As is clear from Table 1, the combination of the component (a) and the component (b) suppressed the decomposition of the component (a) and improved the stability.

Examples 10 to 16 and Comparative Example 8 Of the components shown in Table 2, (a), (b), water and other components were packaged to prepare an agent I (corresponding to the aqueous composition of the present invention).
In addition, hydrogen peroxide (30% by weight aqueous solution) or a hydrogen peroxide releasing body (sodium percarbonate) component and other components are packaged as an agent II, and in some embodiments, potassium carbonate is packaged. III agent. In addition, each compounding ratio was divided and mixed so that the amount of the II or III agent shown in Table 2 became 100% by weight in total. These I
The washing method using the agent, the agent II and the agent III was carried out as follows. Note that the agent I was used after being left in a room at 40 ° C. for one month in a state filled in a closed polypropylene container. Table 2 shows the results. In addition, the compounding amount in Table 2 is based on the total amount including water, and is expressed in weight%. In addition, Dequest 2010 and Dequest 2015DN are both phosphonic acid chelating agents manufactured by Monsanto.

(Cleaning method 1) Inoculated with Cladosporium herbarum, and inoculated at 30 ° C. for 1 hour.
A plastic plate (made of ABS resin) cultured for 4 days was prepared as a model plate. I packaged separately
Agent, II agent or III agent were mixed immediately before use (p at the time of mixing).
H is 10 to 11). 40 μl of these solutions was dropped on a model plate, left for 15 minutes, washed with water and air-dried. Thereafter, the lightness (L value) was measured using a colorimeter 1001DP manufactured by NEC Corporation. The original L value of the plastic plate was 92.4, and the L value of the model plate was 65 to 75. Therefore, the higher the L value, the higher the bleaching and washing property, that is, the higher the mold removal rate.

[0043]

[Table 2]

As is clear from Table 2, the examples are as follows.
Since the decomposition of the component (a) was suppressed, a sufficient bleaching performance was exhibited by the action of the component (a) and the hydrogen peroxide or the hydrogen peroxide releasing material. In Comparative Example 8, since the decomposition rate of the component (a) was higher than that of the examples, the bleaching performance corresponding to the blending amount of the component (c) could not be obtained. From these results, it was confirmed that the cleaning method of the present invention can exhibit high bleaching performance (mold removal performance).

(Cleaning Method 2) Agent I shown in Table 2 (compositions shown in Examples 10 to 16) for the stain on the area of the polyester shirt worn for 3 days
Was applied. Five of these shirts were put together with a commercially available powder detergent (washing liquid concentration: 0.67 g / L) and a bleach containing sodium percarbonate (50% by weight) (0.33 g / L), and a standard for a general fully automatic washing machine. Washing was done on the course. As a comparison, washing was performed under the condition that the aqueous composition was not applied to the stain. After washing, the difference in detergency depending on whether or not the aqueous composition (agent I) was used was examined. As a result, it was found that excellent detergency was obtained by applying the aqueous composition in any of the compositions.

[0046]

According to the aqueous composition of the present invention, the decomposition of the peracid precursor of the component (a) is suppressed by the action of the cationic surfactant of the component (b). Therefore, the bleaching composition for a hard body further containing a bleaching component can sufficiently exhibit the action of the peracid precursor of the component (a), and can maintain high bleaching / cleaning performance.

Continuation of the front page (51) Int.Cl. ⁶ Identification code FI C11D 3:39 3: 395) (72) Inventor Kazunori Tsukuda 1334 Minato, Wakayama-shi, Wakayama Prefecture Kao Corporation Research Center (72) Inventor Makoto Kubo 1334 Minato, Wakayama City, Wakayama Prefecture Inside Kao Research Institute

Claims (4)

[Claims] (1) reacting with hydrogen peroxide in an aqueous solution,
A peracid precursor forming an organic peracid and (b) the following general formula (1): [Wherein, R ¹ represents a linear or branched alkyl group having 1 to 22 carbon atoms, an acyl group, an aryl group, an alkenyl group, an alkoxy group, or a 1 to 8 carbon atom which may be substituted with a hydroxyl group.
A phenyl group or a benzyl group which may be substituted with an alkyl group; R ² represents a linear or branched carbon atom having 1 to 4 carbon atoms which may be substituted with a hydroxyl group and may be interrupted by a carbocyclic ring;
R ³ , R ⁴ and R ^{5 each} represent a hydrogen atom which may be the same or different, a linear or branched alkyl group having 1 to 18 carbon atoms which may be substituted by a hydroxyl group, Acyl group, aryl group, alkenyl group, alkoxy group, phenyl group optionally substituted with alkyl group having 1 to 8 carbon atoms, benzyl group optionally substituted with alkyl group having 1 to 8 carbon atoms, or average addition indicates an alkylene oxide group having 1 to 4 carbon atoms moles ^{1~50, R 3, R 4,} R
^{When 5} is an alkylene oxide group, the alkylene groups to be added may be the same or different and the sequence is arbitrary; X represents an anionic substance such as a halogen anion group or an alkyl sulfate anion group. An aqueous composition comprising a cationic surfactant represented by the formula: 2. The peracid precursor of the component (a) is represented by the following general formula (2): R ⁶ -C (） O) -L (2) wherein R ⁶ is a straight or branched chain An alkyl group, an aryl group, an alkenyl group, an acyl group, which may be any of the following, or the following general formula (3): (Wherein, R ⁷ represents a hydrogen atom, a linear or branched alkyl group, alkenyl group, or acyl group having 1 to 18 carbon atoms;
R ⁸ represents a linear or branched alkylene group having 1 to 8 carbon atoms, p represents 0 or 1; R ⁹ represents a linear or branched alkylene group having 1 to 8 carbon atoms or carbon number A represents a phenylene group which may be substituted by a linear or branched alkyl group having 1 to 5; A represents a linear or branched alkylene group having 1 to 4 carbon atoms; L represents a group represented by the following general formulas (4), (5), and (A represents an average number of moles, 0 to 100, and n A's may be the same or different); 6) or (7): (Wherein, M represents a hydrogen atom, an alkali metal atom or an ammonium group; R ¹⁰ and R ¹¹ represent a linear or branched alkylene group having 1 to 8 carbon atoms) . The aqueous composition according to claim 1, which is represented by the following formula: 3. A cleaning method comprising simultaneously treating the aqueous composition according to claim 1 and a cleaning agent containing hydrogen peroxide or a hydrogen peroxide-releasing substance. 4. A cleaning method comprising applying the aqueous composition according to claim 1 to a surface of a soil, and treating the surface with a cleaning agent containing hydrogen peroxide or a hydrogen peroxide-releasing substance.