JP2017082178A - Liquid detergent for clothing - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a liquid detergent for clothing more excellent in detergency to oily strains.SOLUTION: [1] There is provided a liquid detergent for clothing containing (A) component: a propylene oxide addition product of alcohol, (B) component: a surfactant, (C) component: at least one kind selected from an alkylene oxide addition product (c1) and an alkylene oxide addition product of polyalkylene amine (2). [2] There is provided a liquid detergent for clothing having mass ratio of the (A) component and the (C) component (A/C) of 0.1 to 4. [3] There is provided a liquid detergent for clothing containing having mass ratio of the (B) component and the (A) component (B/A) of 5 to 90. [4] There is provided a liquid detergent for clothing, wherein the (B) component contains a nonionic surfactant and an anionic surfactant and the content of the nonionic surfactant is more than that of the anionic surfactant.SELECTED DRAWING: None

Description

  The present invention relates to a liquid cleaning agent for clothing.

Conventionally, detergents have been proposed that have excellent detergency against hard-to-remove stains such as spilled dirt, mud stains, sebum stains on collar sleeves, and lipstick stains.
For example, as a detergent excellent in detergency against oily dirt such as lipstick dirt, Patent Document 1 discloses a detergent composition comprising an alkyl sulfate surfactant and an anionic surfactant system containing an alcohol ethoxy sulfate surfactant. Things are listed. Patent Document 2 describes a detergent composition comprising a cleaning polymer having a specific amount of a hydrophilic main chain and at least one hydrophobic pendant group.

Special table 2014-531506 gazette Special table 2008-540813

However, the techniques of Patent Documents 1 and 2 are not satisfactory in terms of detergency against oily dirt. In particular, the detergency against stains with stronger lipophilicity such as oil-based ink stains was not sufficient.
Also, when providing a liquid detergent, liquid stability is required so that the liquid detergent does not solidify or precipitate when stored in an environment of normal temperature or low temperature (for example, 5 to 35 ° C.). It is done.

  This invention is made | formed in view of the said situation, and aims at the liquid detergent for clothes which is excellent in the detergency with respect to oily dirt.

  The inventors of the present invention provide that the liquid detergent containing the following components (A) to (C) exhibits (i) an excellent detergency against oily stains such as ink stains, and (ii) the liquid in advance. Washing multiple times with a cleaning agent further increases the cleaning power against oily stains such as ink stains attached thereafter, and (iii) a good liquid even when the surfactant concentration is increased as a concentrated type The inventors have found that stability can be easily obtained, and have completed the present invention. That is, the present invention is as follows.

[1] Component (A): propylene oxide adduct of alcohol, component (B): surfactant, component (C): alkylene oxide adduct of polyalkyleneimine (c1) and alkylene oxide addition of polyalkyleneamine A liquid detergent for clothing, comprising at least one selected from the body (c2).
[2] The liquid cleaning agent for clothing according to the above [1], wherein the mass ratio (A / C) of the component (A) to the component (C) is 0.1 to 4.
[3] The liquid detergent for clothing according to the above [1] or [2], wherein the mass ratio (B / A) of the component (B) to the component (A) is 5 to 90.
[4] The above-mentioned [1] to [3], wherein the component (B) contains a nonionic surfactant and an anionic surfactant, and the content of the nonionic surfactant is larger than that of the anionic surfactant. The liquid cleaning agent for clothes as described in any one of these.

[5] The liquid detergent for clothing according to any one of [1] to [4] above, wherein the component (B) contains two or more kinds of nonionic surfactants.
[6] Content of (B) component with respect to the gross mass of the liquid cleaning agent for clothing is 30 mass% or more, For clothes as described in any one of said [1]-[5] characterized by the above-mentioned. Liquid detergents are preferred.

  ADVANTAGE OF THE INVENTION According to this invention, the liquid cleaning agent for clothes which has the outstanding cleaning power with respect to oil-based stains, such as oil-based ink, can be provided.

(Liquid detergent for clothing)
The liquid detergent for clothes of the present invention (hereinafter also simply referred to as “liquid detergent”) is a composition containing the components (A) to (C).

<(A) component>
Component (A) is a propylene oxide adduct of alcohol.
Propylene oxide adducts of alcohol include monoalcohols such as methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol and octanol; diols such as ethanediol, triols such as glycerol, tetraols such as erythritol, hexaols such as sorbitol It is obtained by adding propylene oxide to a polyhydric alcohol such as oar.

  As the component (A), for example, polyoxypropylene methyl ether, polyoxypropylene ethyl ether, polyoxypropylene propyl ether, polyoxypropylene butyl ether, polyoxypropylene pentyl ether, polyoxypropylene hexyl ether, polyoxypropylene heptyl ether, poly Examples thereof include oxypropylene octyl ether, polyoxypropylene ethylene glycol ether, polyoxypropylene glyceryl ether, polyoxypropylene pentaerythritol ether, and polyoxypropylene sorbitol. Moreover, what is represented by the following formula | equation (I)-(III) for (A) component is preferable.

In formula (I), R ¹ represents a hydrocarbon group having 1 to 8 carbon atoms, a is a number of 10 to 350 representing the average number of repetitions of PO, and PO represents an oxypropylene group.
The number of carbon atoms in R ¹ is 1-4 preferably 1 to 3 is more preferable.
R ¹ is preferably an alkyl group or an alkylene group, and more preferably a methyl group, an ethyl group, a propyl group, or a butyl group.
a is preferably 20 to 150.

In formula (II), b and c are each independently a number of 10 to 350 representing the average number of repetitions of PO, and PO represents an oxypropylene group.
It is preferable that b and c are independently 10-80.

In formula (III), d, e, and f are each independently a number of 10 to 350 that represents the average number of repetitions of PO, and PO represents an oxypropylene group.
d, e, and f are preferably independently 6 to 50.

  Of the formulas (I) to (III), the compounds represented by the formula (II) or the formula (III) are preferable because of their excellent detergency and liquid stability against oily stains such as ink stains. The compound represented by these is more preferable.

(A) As for the weight average molecular weight of a component, 1500-6000 are preferable, 2500-5500 are more preferable, 3000-5000 are more preferable.
If it is more than the said lower limit, the cleaning power with respect to oil-based stains, such as ink stains, will become easier to improve. If it is below the said upper limit, liquid stability will improve more easily.

  In addition, the weight average molecular weight of (A) component is calculated | required from the molecular weight distribution obtained by GPC (gel permeation chromatography) which used polypropylene glycol (weight average molecular weight: 800, 1200, 2000, 4000) as a standard.

As a method for producing a compound represented by the formula (I), for example, known methods for addition polymerization of propylene oxide to an alcohol (R 1 ^-OH) is.
As a manufacturing method of the compound represented by Formula (II), the well-known method of carrying out addition polymerization of propylene oxide to ethylene glycol is mentioned, for example.
As a manufacturing method of the compound represented by Formula (III), the well-known method of carrying out addition polymerization of propylene oxide to glycerol is mentioned, for example.
When addition polymerization is performed on each compound, a propylene oxide adduct having a desired weight average molecular weight can be produced by adjusting the supply amount of propylene oxide.

The component (A) contained in the liquid cleaning agent of the present invention may be one type or two or more types.
The content of the component (A) is preferably 0.5 to 5% by mass, more preferably 0.75 to 3% by mass, and 0.75 to 1.5% by mass with respect to the total mass of the liquid detergent. Further preferred.
If it is more than the said lower limit, the cleaning power with respect to oil-based stains, such as ink stains, will become easier to improve. If it is below the said upper limit, liquid stability will improve more easily.

<(B) component>
Component (B) is a surfactant. As (B) component of this invention, the well-known surfactant currently used as a washing | cleaning component of a well-known detergent, for example, anionic surfactant, nonionic surfactant, cationic surfactant, amphoteric surfactant, semipolar A surfactant or the like is applicable.
Among these, from the viewpoint of enhancing the detergency against oily stains such as ink stains of the present invention, it is preferable to contain at least one of anionic surfactants and nonionic surfactants, and more preferably to contain both. .

[Nonionic surfactant]
Examples of known nonionic surfactants applicable as the component (B) include the following (1) to (8).
(1) An average of 3 to 30 moles, preferably 3 to 20 moles, more preferably 3 to 20 moles of an alkylene oxide having 2 to 4 carbon atoms in an aliphatic alcohol having 6 to 22 carbon atoms, preferably 8 to 18 carbon atoms, more preferably 9 to 18 carbon atoms. Is a polyoxyalkylene alkyl (or alkenyl) ether added in an amount of 5 to 20 mol. Among these, polyoxyethylene alkyl (or alkenyl) ether and polyoxyethylene polyoxypropylene alkyl (or alkenyl) ether are preferable. Examples of the aliphatic alcohol used here include primary alcohols and secondary alcohols. The alkyl group may have a branched chain. As the aliphatic alcohol, a primary alcohol is preferable. However, those corresponding to component (A) are excluded.
(2) Polyoxyethylene alkyl (or alkenyl) phenyl ether.
(3) A fatty acid alkyl ester alkoxylate in which an alkylene oxide is added between ester bonds of a long-chain fatty acid alkyl ester.
(4) Polyoxyethylene sorbitan fatty acid ester.
(5) Polyoxyethylene sorbite fatty acid ester.
(6) Polyoxyethylene fatty acid ester.
(7) Polyoxyethylene hydrogenated castor oil.
(8) Glycerin fatty acid ester.

  As the nonionic surfactant, the above (1) or (3) is preferable, and among them, those represented by the following formula (V) or (VI) are preferable.

_{^{R 2 -C (= O) O}} - [(EO) s / (PO) t] - (EO) u -R 3 ··· (V)

In the formula (V), R ² is a hydrocarbon group having 7 to 22 carbon atoms, R ³ is an alkyl group having 1 to 6 carbon atoms, and s is a number of 6 to 20 representing the average number of repetitions of EO. Yes, t is a number of 0 to 6 representing the average number of repetitions of PO, u is a number of 0 to 20 representing the average number of repetitions of EO, EO represents an oxyethylene group, PO represents an oxypropylene group Represent.

In Formula (V), at the number of carbon atoms in ^{R 2} is preferably 9 to 21, 11 to 21 is more preferable.
R ² is preferably an alkyl group or an alkenyl group.
R ² may be linear or branched.
From the viewpoint of further improving detergency, R ² is preferably a linear or branched alkyl group having 7 to 22 carbon atoms, or a linear or branched chain alkenyl group having 7 to 22 carbon atoms.

In formula (V), the alkyl group of R ³ may be either a straight chain or a branched chain, and is preferably a methyl group or an ethyl group.

  In formula (V), 6-20 are preferable, as for s + u, 6-18 are more preferable, and 11-18 are more preferable. If it is more than the said lower limit, liquid stability will become easy to improve more. If it is below the said upper limit, cleaning power will improve more easily.

In the formula (V), t is preferably 0 to 3, and more preferably 0.
If t is 3 or less, the liquid stability is more likely to be improved.
When t is 1 or more, in [(EO) _s / (PO) _t ], the oxyethylene group and the oxypropylene group may be random polymerization or block polymerization.

^{_{R 4 -O - [(EO)}} v / (PO) z] - (EO) x -H ··· (VI)

In the formula (VI), R ⁴ is a hydrocarbon having 6 to 22 carbon atoms, v is a number of 3 to 20 representing the average number of repetitions of EO, and z is a number of 0 to 6 representing the average number of repetitions of PO. And x is a number from 0 to 20 representing the average number of repetitions of EO, EO represents an oxyethylene group, and PO represents an oxypropylene group.

In formula (VI), the number of carbon atoms of R ⁴ is preferably 10 to 22, more preferably 10 to 20, and still more preferably 10 to 18, from the viewpoint of further improving the detergency.
R ⁴ may be linear or branched.

Preferable R ⁴ —O— includes a group represented by the following general formula (VII).

(R ¹⁰¹ ) (R ¹⁰² ) CH—O— (VII)

In formula (VII), R ¹⁰¹ and R ¹⁰² each independently represent a hydrogen atom or a chain hydrocarbon group.
The total carbon number of R ¹⁰¹ and R ¹⁰² is 5 to 21, preferably 9 to 21, more preferably 9 to 19, and still more preferably 9 to 17.
R ¹⁰¹ and R ¹⁰² may each independently be a straight chain or a branched chain.

In Formula (VI), R ⁴ is a linear alkyl group, and it is preferable that an etheric oxygen atom (—O—) represented by Formula (VI) is bonded to the secondary carbon atom of R ⁴ . .

  In formula (VI), v + x is preferably from 3 to 20, more preferably from 5 to 18, still more preferably from 6 to 18, and particularly preferably from 11 to 18. If it is more than the said lower limit, liquid stability will become easy to improve more. If it is below the said upper limit, cleaning power will improve more easily.

In formula (VI), z is preferably 0-3.
If z is 3 or less, the liquid stability is more likely to be improved.
When z is 1 or more, in [(EO) _v / (PO) _z ], the oxyethylene group and the oxypropylene group may be random polymerization or block polymerization.

The distribution of EO or PO in the formula (V) and the formula (VI) varies depending on the reaction method in production. For example, when ethylene oxide or propylene oxide is added to a raw material using sodium hydroxide, potassium hydroxide or the like, which is a general alkali catalyst, s or t in formula (V) and v in formula (VI) Or the distribution of z is relatively wide. A specific alkoxylation catalyst such as magnesium oxide to which metal ions such as Al ³⁺ , Ga ³⁺ , In ³⁺ , Tl ³⁺ , Co ³⁺ , Sc ³⁺ , La ³⁺ , Mn ^{2+ and the} like described in JP-B-615038 is added. When ethylene oxide or propylene oxide is added to the raw material, the distribution of s or t in formula (V) and v or z in formula (VI) becomes relatively narrow.

  In addition, the average repetition number of EO and PO of each component contained in the liquid detergent of the present invention can be measured by gas chromatography or the like.

  The “narrow ratio” described below indicates a distribution ratio of alkylene oxide adducts having different addition mole numbers of alkylene oxide (AO) having 2 to 4 carbon atoms, and is represented by the following mathematical formula (S).

［式中、ｎ_ｍａｘは、全体のアルキレンオキシド付加体中に最も多く存在するアルキレンオキシド付加体のＡＯの付加モル数を示す。ｉはＡＯの付加モル数を示す。Ｙｉは全体のアルキレンオキシド付加体中に存在する、ＡＯの付加モル数がｉであるアルキレンオキシド付加体の割合（質量％）を示す。］

[ _Wherein n _max represents the number of moles of AO added to the alkylene oxide adduct most present in the entire alkylene oxide adduct. i represents the number of moles of AO added. Yi represents the ratio (mass%) of the alkylene oxide adduct present in the entire alkylene oxide adduct and having an added mole number of AO of i. ]

  Addition of components that do not contribute to detergency to the product obtained by synthesizing the nonionic surfactant represented by formula (V), for example, fatty acid ester of raw material, or alkylene oxide addition in which s of formula (V) is 1 or 2 When the body coexists, the narrow rate tends to decrease. On the other hand, when the narrow ratio is high, there are few unnecessary components that coexist, and there is a tendency that the detergency of the cleaning power and the problem of raw material odor are less likely to occur. The same applies to the nonionic surfactant represented by the formula (VI).

20 mass% or more is preferable and, as for the narrow rate of the nonionic surfactant represented by Formula (V) and (VI), 25 mass% or more is more preferable.
When the narrow ratio is 20% by mass or more, particularly 25% by mass or more, it becomes easy to obtain a liquid cleaning agent with less raw material odor of the surfactant.
Further, the higher the narrow rate, the better the detergency can be obtained. Therefore, the narrow rate may be 100% by mass, but it is often 80% by mass or less in a normal manufacturing method.
The narrow rate is preferably 20 to 50% by mass and more preferably 20 to 40% by mass because the liquid stability and detergency of the liquid detergent are improved.

The narrow rate can be controlled by the method for producing the nonionic surfactant.
As a suitable method for producing the nonionic surfactant represented by the formula (V), for example, a method in which ethylene oxide is addition-polymerized to a fatty acid alkyl ester using a surface-modified composite metal oxide catalyst (Japanese Patent Application Laid-Open No. 2000-2000). -144179)).
As a suitable method for producing the nonionic surfactant represented by the formula (VI), for example, a method of addition-polymerizing ethylene oxide to an alcohol having 6 to 22 carbon atoms using a surface-modified composite metal oxide catalyst Is mentioned.

Examples of the surface-modified suitable composite metal oxide catalyst include, for example, metal ions (Al ³⁺ , Ga ³⁺ , In ³⁺ , Tl ³⁺ , Co ³⁺ , Sc ³⁺ , surface modified with a metal hydroxide or the like, La ³⁺ , Mn ^2+, etc.) added to the composite metal oxide catalyst such as magnesium oxide, hydrotalcite calcined catalyst whose surface is modified with metal hydroxide and / or metal alkoxide, and the like.
In the surface modification of the composite metal oxide catalyst, it is preferable to use a composite metal oxide in combination with a metal hydroxide and / or a metal alkoxide. In this case, the ratio of the metal hydroxide and / or metal alkoxide is preferably 0.5 to 10 parts by mass and more preferably 1 to 5 parts by mass with respect to 100 parts by mass of the composite metal oxide. .

The nonionic surfactant as the material of the liquid detergent of the present invention may be a commercially available product or a product obtained by a known production method.
The nonionic surfactant represented by the formula (V) can be produced, for example, by a known method in which ethylene oxide and / or propylene oxide is added to a fatty acid alkyl ester.
The nonionic surfactant represented by the formula (VI) can be produced, for example, by a known method of addition polymerization of ethylene oxide and / or propylene oxide to an alcohol having 6 to 22 carbon atoms.

As the nonionic surfactant as the component (B), it is preferable to include a compound (that is, polyoxyethylene fatty acid alkyl ester) in which t in the formula (V) is 0. In particular, it is preferable to include polyoxyethylene fatty acid methyl ester (hereinafter referred to as “MEE”) in which R ³ in formula (V) is a methyl group. If these suitable nonionic surfactants are contained, the detergency and liquid stability of the liquid detergent of the present invention are further improved.

The nonionic surfactant as the component (B) contained in the liquid cleaning agent of the present invention may be one type or two or more types.
From the viewpoint of enhancing the detergency, it is preferable that two or more nonionic surfactants are blended. In particular, since both MEE and polyoxyethylene alkyl ether such as LMAO are blended, the detergency is further improved and the liquid stability is further improved, which is more preferable.

The concentration of the component (B) relative to the total mass of the liquid cleaning agent of the present invention may be about 25% by mass (regular type) or may be more than 40% by mass (super concentrated type). In the case of the ultra-concentrated type, a method of applying and cleaning a liquid cleaning agent directly on clothes (application cleaning) is preferable from the viewpoint of enhancing the cleaning power.
In general, it is known that a surfactant may precipitate in a liquid detergent having an ultra-concentrated composition. However, in the liquid cleaning agent of the present invention, when MEE is included, precipitation of the surfactant can be suppressed and the liquid stability can be improved.

  10-50 mass% is preferable, as for the density | concentration of the nonionic surfactant as (B) component with respect to the total mass of the liquid cleaning agent of this invention, 15-45 mass% is more preferable, and 20-40 mass% is further more preferable. Within the above range, the balance between cleaning power and liquid stability is good.

The content of the nonionic surfactant in the component (B) is preferably 10 to 80% by mass, more preferably 15 to 75% by mass, and still more preferably 20 to 70% by mass with respect to the total mass of the component (B). .
If it is more than the said lower limit, the cleaning power with respect to oil-based stains, such as ink stains, will become easier to improve. If it is below the said upper limit, liquid stability will improve more easily.

[Anionic surfactant]
As a well-known anionic surfactant applicable as (B) component, the following (1)-(12) is mentioned, for example.
(1) A methyl, ethyl or propyl ester salt of a saturated or unsaturated α-sulfo fatty acid having 8 to 20 carbon atoms.
(2) Linear or branched alkylbenzene sulfonate (LAS or ABS) having an alkyl group having 8 to 18 carbon atoms.
(3) Alkane sulfonate having 10 to 20 carbon atoms.
(4) C-C20 α-olefin sulfonate (AOS).
(5) Alkyl sulfate or alkenyl sulfate (AS) having 10 to 20 carbon atoms.
(6) Any one of alkylene oxides having 2 to 4 carbon atoms, or ethylene oxide (EO) and propylene oxide (PO) (molar ratio EO / PO = 0.1 / 9.9 to 9.9 / 0.1) Polyoxyalkylene alkyl (or alkenyl) ether sulfate (AES) having a linear or branched alkyl (or alkenyl) group having 10 to 20 carbon atoms added with an average of 0.5 to 10 mol.
(7) Any one of alkylene oxides having 2 to 4 carbon atoms, or ethylene oxide and propylene oxide (molar ratio EO / PO = 0.1 / 9.9 to 9.9 / 0.1), average 3 to 30 mol An alkyl (or alkenyl) phenyl ether sulfate having an added linear or branched alkyl (or alkenyl) group having 10 to 20 carbon atoms.
(8) Any one of alkylene oxides having 2 to 4 carbon atoms, or ethylene oxide and propylene oxide (molar ratio EO / PO = 0.1 / 9.9 to 9.9 / 0.1), an average of 0.5 to An alkyl (or alkenyl) ether carboxylate having a linear or branched alkyl (or alkenyl) group having 10 to 20 carbon atoms added with 10 moles.
(9) Alkyl polyhydric alcohol ether sulfates such as alkyl glyceryl ether sulfonic acids having 10 to 20 carbon atoms.
(10) Long-chain (C8-20) monoalkyl, dialkyl or sesquialkyl phosphates.
(11) Polyoxyethylene monoalkyl, dialkyl or sesquialkyl phosphate.
(12) Soap. A higher fatty acid salt having an average carbon number of 10 to 20 (preferably having 12 to 18 carbon atoms).

  Other than the above, for example, carboxylic acid type anionic surfactants such as alkyl ether carboxylate, polyoxyalkylene ether carboxylate, alkylamide ether carboxylate, alkenylamide ether carboxylate, acylaminocarboxylate; alkyl Examples thereof include phosphoric acid ester type anionic surfactants such as phosphoric acid ester salts, polyoxyalkylene alkyl phosphoric acid ester salts, polyoxyalkylene alkyl phenyl phosphoric acid ester salts and glycerin fatty acid ester monophosphoric acid ester salts.

As the anionic surfactant, the above (2) or (6) is preferable.
The polyoxyalkylene alkyl ether sulfate (6) is preferably a compound represented by the general formula (IV).

^{_{R 40 -O - [(EO)}} m / (PO) n] -SO 3 - M + ··· (IV)

In the formula (IV), R ⁴⁰ is a linear or branched alkyl group having 8 to 20 carbon atoms, EO represents an oxyethylene group, PO represents an oxypropylene group, and m represents EO. It is a number of 1 or more representing the average number of repetitions, n is a number of 0 to 6 representing the average number of repetitions of PO, and M ⁺ is a counter cation.

  The content of the component (b0) where m = 0 and n = 0 in the formula (IV) is preferably 35 to 55% by mass with respect to the total mass of the component (B).

As the polyoxyalkylene alkyl ether sulfate of (6), those having a linear or branched alkyl group having 10 to 20 carbon atoms and having an average of 1 to 5 moles of alkylene oxide added are preferred.
As carbon number of the said alkyl group, 10-20 are preferable and 12-14 are more preferable. Specifically, a dodecyl group, a tridecyl group, a tetradecyl group, etc. are mentioned. Of these, a dodecyl group is preferable.
1-5 are preferable and, as for the average repeating number of EO of (6), 1-3 are more preferable.
As for the average number of repetitions of PO of (6), 0-3 are preferable.

  Examples of the salt form of the anionic surfactant include alkali metal salts such as sodium salts and potassium salts; alkaline earth metal salts such as magnesium salts; alkanolamine salts such as monoethanolamine salts and diethanolamine salts; ammonium salts and the like. It is done. Of these, alkali metal salts are preferred.

The anionic surfactant can be produced by a known method.
Examples of the method for producing LAS include a method of sulfonating alkylbenzene with sulfuric anhydride and neutralizing with alkali.
Examples of the method for producing AES include a method in which polyoxyalkylene alkyl ether is reacted with sulfuric anhydride; a method in which chlorosulfonic acid is reacted to sulfonate and neutralize with an alkali.

1 type may be sufficient as the anionic surfactant as (B) component contained in the liquid cleaning agent of this invention, and 2 or more types may be sufficient as it.
The content of the anionic surfactant in the component (B) is preferably 5 to 50% by mass, more preferably 10 to 45% by mass, and further preferably 10 to 40% by mass with respect to the total mass of the component (B). .
If it is more than the said lower limit, the cleaning power with respect to oil-based stains, such as ink stains, will become easier to improve. If it is below the said upper limit, liquid stability will improve more easily.

[Cationic surfactant]
Examples of known cationic surfactants applicable as component (B) include alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkylbenzyldimethylammonium salts, alkylpyridinium salts, and the like. Examples of these salts include alkali metal salts such as sodium and potassium, alkaline earth metal salts such as magnesium, and alkanolamine salts such as monoethanolamine and diethanolamine.

1 type may be sufficient as the cationic surfactant as (B) component contained in the liquid cleaning agent of this invention, and 2 or more types may be sufficient as it.
(B) 0.1-5 mass% is preferable with respect to the total mass of (B) component, and, as for content of the cationic surfactant in a component, 0.5-4 mass% is more preferable, 1-3 mass % Is more preferable.
If it is more than the said lower limit, the cleaning power with respect to oil-based stains, such as ink stains, will become easier to improve. If it is below the said upper limit, liquid stability will improve more easily.

[Amphoteric surfactant]
Known amphoteric surfactants applicable as the component (B) include, for example, alkyl betaine type, alkyl amide betaine type, imidazoline type, alkyl amino sulfone type, alkyl amino carboxylic acid type, alkyl amide carboxylic acid type, and amide amino acid. And amphoteric surfactants such as phosphoric acid type.
The amphoteric surfactant as the component (B) contained in the liquid cleaning agent of the present invention may be one type or two or more types.

  The component (B) of the liquid detergent of the present invention preferably contains a nonionic surfactant and an anionic surfactant. The content ratio of the nonionic surfactant / anionic surfactant in the component (B) is preferably 0.1 to 20, more preferably 0.3 to 9, still more preferably 1 to 9, and 1.5 on the mass basis. ~ 4 is particularly preferred. When the above ratio is within this range, the cleaning power against oily stains such as ink stains during coating and cleaning is further improved.

20-70 mass% is preferable with respect to the total mass of a liquid cleaning agent, and, as for content of (B) component in the liquid cleaning agent of this invention, 20-60 mass% is more preferable.
When the component (B) is 20% by mass or more with respect to the total mass of the liquid cleaning agent of the present invention, the detergency against oily stains such as ink stains when used in combination with the components (A) and (C) is sufficient. Enhanced. Furthermore, 30 mass% or more is preferable, as for content of (B) component, 35 mass% or more is more preferable, and 40 mass% or more is especially preferable.
When the content of the component (B) is 30% by mass or more, a particularly excellent cleaning power can be obtained as a concentrated liquid cleaning agent in coating cleaning.
On the other hand, from the viewpoint of increasing the liquid stability of the liquid detergent, the component (B) is preferably 70% by mass or less, and more preferably 60% by mass or less.

<(C) component>
Component (C) is at least one selected from the alkylene oxide adduct (c1) of polyalkyleneimine and the alkylene oxide adduct (c2) of polyalkyleneamine.
In the liquid cleaning agent of the present invention, the detergency against oily stains such as ink stains is further enhanced by the combined use of the component (C) and the component (A). In particular, when the treatment is repeated with the liquid detergent of the present invention, the effect is remarkable.

The component (c1) is an alkylene oxide adduct of polyalkyleneimine.
The polyalkyleneimine is represented by the following general formula (II).
NH ₂ —R ²¹ — (NA—R ²¹ ) _n —NH ₂ (II)
In formula (II), each R ²¹ independently represents an alkylene group having 2 to 6 carbon atoms, A represents a hydrogen atom or another polyamine chain by branching, and n is a number of 1 or more. However, not all of the A are hydrogen atoms.

R ²¹ is a linear alkylene group having 2 to 6 carbon atoms or a branched alkylene group having 3 to 6 carbon atoms. R ²¹ is preferably an alkylene group having 2 to 4 carbon atoms, and more preferably an alkylene group having 2 carbon atoms.

The polyalkyleneimine can be obtained by polymerizing one or more of alkyleneimines having 2 to 6 carbon atoms by a conventional method. Examples of the alkyleneimine having 2 to 6 carbon atoms include ethyleneimine, propyleneimine, 1,2-butyleneimine, 2,3-butyleneimine, 1,1-dimethylethyleneimine and the like.
As polyalkyleneimine, polyethyleneimine (PEI) and polypropyleneimine are preferable, and PEI is more preferable. PEI is obtained by polymerizing ethyleneimine and has a branched chain structure containing primary, secondary and tertiary amine nitrogen atoms in the structure.

The weight average molecular weight of the polyalkyleneimine is preferably 200 to 2000, more preferably 300 to 1500, still more preferably 400 to 1000, and particularly preferably 500 to 800.
The weight average molecular weight of the component (C) is a value obtained by gel permeation chromatography (GPC) using polyethylene glycol as a standard substance.

  As polyalkyleneimine, those having 5 to 30 active hydrogens in one molecule are preferable, those having 7 to 25 are more preferable, and those having 10 to 20 are more preferable.

The component (c1) is obtained by adding alkylene oxide to polyalkyleneimine. As this method, for example, an alkylene oxide such as ethylene oxide is added to a polyalkyleneimine which is a starting material in the presence of a basic catalyst such as sodium hydroxide, potassium hydroxide or sodium methylate at 100 to 180 ° C. And the like.
Examples of the alkylene oxide include alkylene oxides having 2 to 4 carbon atoms. Examples of the alkylene oxide include ethylene oxide, propylene oxide, and butylene oxide. Ethylene oxide and propylene oxide are preferable, and ethylene oxide is more preferable.

Examples of the alkylene oxide adduct of polyalkyleneimine include an ethylene oxide adduct of polyalkyleneimine, a propylene oxide adduct of polyalkyleneimine, and an ethylene oxide-propylene oxide adduct of polyalkyleneimine. In addition, the ethylene oxide-propylene oxide adduct of polyalkyleneimine is obtained by adding ethylene oxide and propylene oxide to polyalkyleneimine, and the addition order and addition form of ethylene oxide and propylene oxide to polyalkyleneimine (block shape, random shape). ) Is optional.
As the alkylene oxide adduct of polyalkyleneimine, an ethylene oxide adduct of polyalkyleneimine and an ethylene oxide-propylene oxide adduct of polyalkyleneimine are preferable, and an ethylene oxide adduct of polyalkyleneimine is more preferable.

  The alkylene oxide adduct of polyalkyleneimine is preferably an average of 5 to 40 alkylene oxides added to one active hydrogen atom of the starting polyalkyleneimine, and an average of 10 to 30 alkylene oxides. Those with added are preferred. That is, it is preferable that an average of 5 to 40 mol of alkylene oxide is added per 1 mol of active hydrogen of the polyalkyleneimine as a raw material, and an average of 10 to 30 mol of alkylene oxide is preferable.

1000-80000 are preferable, as for the weight average molecular weight of the alkylene oxide adduct of polyalkyleneimine, 2000-50000 are more preferable, 5000-30000 are further more preferable, and 10000-20000 are especially preferable.
Examples of the alkylene oxide adduct of polyalkyleneimine include compounds represented by the formula (II-a).

In formula (II-a), R ³² is each independently an alkylene group having 2 to 6 carbon atoms, and m is independently a number of 1 or more.
R ³² is preferably an alkylene group having 2 or 3 carbon atoms, and more preferably an alkylene group having 2 carbon atoms.
m is the average number of repetitions of (R ³² O), preferably 5 to 40, more preferably 10 to 30.
As the alkylene oxide adduct of polyalkyleneimine, a synthetic product or a commercially available product may be used.
As a commercial item, the brand name "Sokalan HP20" by BASF, etc. are mentioned, for example.

The component (c2) is an alkylene oxide adduct of polyalkyleneamine.
The polyalkyleneamine is represented by the following general formula (III).
NH ₂ (R ³¹ NH) ₁ H (III)
In the formula (III), R ³¹ is an alkylene group having 2 to 6 carbon atoms, and l is a number of 1 or more.

R ³¹ is a linear alkylene group having 2 to 6 carbon atoms or a branched alkylene group having 3 to 6 carbon atoms. R ³¹ is preferably an alkylene group having 2 to 4 carbon atoms, and more preferably an alkylene group having 2 carbon atoms.

  As the polyalkyleneamine, polyethyleneamine is preferable. Examples of polyethyleneamine include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine. These polyethyleneamines can be obtained by a known production method, for example, by reacting ammonia and ethylene dichloride.

  The weight average molecular weight of the polyalkyleneamine is preferably 60 to 1800, more preferably 60 to 1000, and still more preferably 60 to 800.

  As the polyalkyleneamine, those having 6 to 30 active hydrogens in one molecule are preferable, and those having 7 to 20 active hydrogens are more preferable.

  The component (c2) is obtained by adding alkylene oxide to polyalkyleneamine. This reaction can be performed in the same manner as the component (c1). Examples of the alkylene oxide include alkylene oxides having 2 to 4 carbon atoms. Examples of the alkylene oxide include ethylene oxide, propylene oxide, and butylene oxide. Ethylene oxide and propylene oxide are preferable, and ethylene oxide is more preferable.

Examples of the alkylene oxide adduct of polyalkyleneamine include an ethylene oxide adduct of polyalkyleneamine, a propylene oxide adduct of polyalkyleneamine, and an ethylene oxide-propylene oxide adduct of polyalkyleneamine.
The alkylene oxide adduct of polyalkyleneamine is preferably an ethylene oxide adduct of polyalkyleneamine or an ethylene oxide-propylene oxide adduct of polyalkyleneamine, more preferably an ethylene oxide adduct of polyalkyleneamine.

  The alkylene oxide adduct of polyalkyleneamine is preferably an average of 5 to 40 alkylene oxides added per active hydrogen atom of polyalkyleneamine as a raw material, and average 10 to 30 alkylene oxides. Those with added are preferred. That is, an average of 5 to 40 mol of alkylene oxide is preferably added per mol of active hydrogen of the polyalkyleneamine as a raw material, and an average of 10 to 30 mol of alkylene oxide is preferable.

  1000-80000 is preferable, as for the weight average molecular weight of the alkylene oxide adduct of polyalkyleneamine, 2000-50000 is more preferable, 5000-30000 is further more preferable, and 10000-20000 is especially preferable.

As the component (C), the component (c1) is preferable. Among the components (c1), an ethylene oxide adduct of polyethyleneimine is preferable.
As the component (C), any one type may be used alone, or two or more types may be used in combination.

The content of the component (C) is preferably 0.01 to 5% by mass, more preferably 0.05 to 3% by mass, and 0.1 to 2% by mass with respect to the total mass of the liquid detergent of the present invention. Is more preferable.
If the component (C) is 0.01% by mass or more, the detergency against oily stains such as ink is improved, and if it is 5% by mass or less, the liquid stability is good.

In the liquid detergent of the present invention, the mass ratio (A / C) of the component (A) / component (C) is preferably 0.1 to 4, more preferably 0.2 to 2.5, and 0.3 to 1.5 is more preferable.
When the mass ratio of the component (A) / component (C) is in the above range, the detergency against oily stains such as ink is further improved.

In the liquid detergent of the present invention, the mass ratio (B / A) of the component (B) / component (A) is preferably 5 to 90, more preferably 10 to 80, and still more preferably 15 to 60.
When the mass ratio of component (B) / component (A) is in the above range, the liquid stability is further improved.

<Optional component>
The liquid detergent of the present invention includes a solvent such as water, an enzyme such as protease (for example, alcalase and coronase), a water-miscible organic solvent such as ethanol, an alkaline agent such as monoethanolamine, and an antioxidant such as dibutylhydroxytoluene. Agents, preservatives such as sodium benzoate, enzyme stabilizers such as calcium chloride and sodium lactate, fragrances, pigments and the like.

  The liquid detergent of the present invention preferably has a pH at 25 ° C. of 4 to 9, more preferably pH 6 to 9. When the pH is in such a range, the liquid stability of the liquid detergent can be maintained well. pH can be adjusted by mix | blending a pH adjuster as needed. The pH adjuster is optional as long as the effects of the present invention are not impaired, but sulfuric acid, sodium hydroxide, potassium hydroxide, alkanolamine and the like are preferable. The pH is a value measured at 25 ° C. according to JIS Z8802: 2011.

  As a manufacturing method of the liquid detergent of this invention, the method of adding the said (A)-(C) component to water which is a solvent, adding an arbitrary component as needed, and mixing this is mentioned. .

Examples of the method of using the liquid cleaning agent of the present invention include a method in which the liquid cleaning agent is poured into water together with the object to be washed at the time of washing, and a cleaning agent aqueous solution prepared by dissolving the liquid cleaning agent in water in advance. For example, a method of immersing the washing product. Alternatively, the liquid cleaning agent may be applied directly to the article to be washed and left for a certain period of time, and then normal washing may be performed (application cleaning).
In addition, when using a liquid cleaning agent melt | dissolving in water, it is preferable to dilute, for example by 5 to 5000 times (volume basis).

  As described above, since the liquid detergent of the present invention contains the components (A) to (C), it is excellent in liquid stability and detergency against oily dirt such as ink.

In the liquid detergent of the present invention, the component (A) is preferably polyoxypropylene glyceryl ether, and the component (C) is preferably an alkylene oxide adduct of polyalkyleneimine.
In the liquid cleaning agent of the present invention, the component (A) is preferably polyoxypropylene glyceryl ether, and the component (B) is preferably two or more nonionic surfactants.
In the liquid detergent of the present invention, the component (A) is preferably polyoxypropylene glyceryl ether, and the component (B) is preferably two or more types of nonionic surfactants and one or more types of anionic surfactants. .
In the liquid detergent of the present invention, the component (A) is polyoxypropylene glyceryl ether, the component (B) is two or more nonionic surfactants and one or more anionic surfactants, and It is preferable that the total content of the nonionic surfactant is larger than the total content of the anionic surfactant.
In the preferred case of the above components (A) and (B), the component (C) is more preferably an alkylene oxide adduct of polyalkyleneimine.

Hereinafter, the present invention will be described in more detail using examples, but the present invention is not limited to these examples. In this example, “%” indicates “% by mass” unless otherwise specified.
The composition of the liquid detergent for clothing in each example is shown in Tables 1-2.
The raw materials used in this example are as follows.

<(A) component>
A-1: polyoxypropylene glyceryl ether, Actol T-1500 (trade name), manufactured by Mitsui Chemicals, Inc., weight average molecular weight 1500.
A-2: polyoxypropylene glyceryl ether, Actol T-3000 (trade name), manufactured by Mitsui Chemicals, Inc., weight average molecular weight 3000.
A-3: polyoxypropylene glyceryl ether, Actol T-4000 (trade name), manufactured by Mitsui Chemicals, Inc., weight average molecular weight 4000.
A-4: Polyoxypropylene glyceryl ether, Actol T-5000 (trade name), manufactured by Mitsui Chemicals, Inc., weight average molecular weight 5000.
A-5: Polyoxypropylene ethylene glycol ether, Actol D-3000 (trade name), manufactured by Mitsui Chemicals, Inc., weight average molecular weight 3000.
A-6: Polyoxypropylene ethylene glycol ether, Actol D-4000 (trade name), manufactured by Mitsui Chemicals, Inc., weight average molecular weight 4000.

<(B) component: surfactant>
B-1: MEE (polyoxyethylene fatty acid methyl ester). A product obtained by adding 15 moles of ethylene oxide to a coconut fatty acid methyl (mixture of methyl laurate / methyl myristate = 74/26 by mass ratio) using an alkoxylation catalyst. In the general formula (V), R ² = alkyl group having 11 carbon atoms and alkyl group having 13 carbon atoms, R ³ = methyl group, s = 15, t = 0, u = 0. Synthesized by the following synthesis method.

[Method for synthesizing B-1]
The synthesis was performed according to the synthesis method described in JP-A No. 2000-144179.
Alumina-magnesium hydroxide (Kyoward 300 (trade name), manufactured by Kyowa Chemical Industry Co., Ltd.) having a composition of 2.5 MgO.Al ₂ O ₃ .wH ₂ O (w: moles of hydrated water) is 600 ° C. And calcining in a nitrogen atmosphere for 1 hour to obtain a calcined alumina / magnesium hydroxide (unmodified) catalyst. An autoclave was charged with 2.2 g of calcined alumina / magnesium hydroxide (unmodified) catalyst, 2.9 mL of 0.5N potassium hydroxide ethanol solution, 280 g of lauric acid methyl ester, and 70 g of myristic acid methyl ester in a 4 L autoclave. The catalyst was reformed inside. Next, after the inside of the autoclave was replaced with nitrogen, 1052 g of ethylene oxide was introduced and reacted while stirring while maintaining the temperature at 180 ° C. and the pressure at 0.3 MPa.
The obtained reaction liquid was cooled to 80 ° C., 159 g of water and 5 g of activated clay and diatomaceous earth as filter aids were added and mixed, and then the catalyst was filtered off to obtain B-1.
The narrow rate of B-1 was 30 mass%.

-B-2: MEE. A product obtained by adding ethylene oxide equivalent to 15 moles to methyl coconut fatty acid (mixture of methyl laurate / methyl myristate = 8/2 in mass ratio) using an alkoxylation catalyst. In the general formula (V), R ² = alkyl group having 11 carbon atoms and alkyl group having 13 carbon atoms, R ³ = methyl group, s = 15, t = 0, u = 0. Synthesized by the following synthesis method.

[Method for synthesizing B-2]
In a 500 mL beaker, 137 g of 2-ethylhexanol (primary reagent, manufactured by Kanto Chemical Co., Inc.) and 41.7 g of calcium acetate monohydrate (special grade reagent, manufactured by Kanto Chemical Co., Ltd.) were placed, and the room temperature (25 (° C.) to obtain a dispersion (dispersing step). While stirring the dispersion, 20.9 g of sulfuric acid (special grade reagent, manufactured by Kanto Chemical Co., Inc.) was added and mixed for 10 minutes with a dropping funnel (mixing step). In the mixing step, heat generation was caused by the addition of sulfuric acid, so the beaker was cooled in a water bath and the reaction temperature was controlled at 30-50 ° C. After adding sulfuric acid, the mixture was further stirred for 2 hours while maintaining at 50 ° C. (catalyst aging step) to obtain an alkoxylation catalyst.
Into an autoclave, 12.5 g of the alkoxylation catalyst, 462 g of methyl laurate (Pastel M12, manufactured by Lion Chemical Co., Ltd.) and 166 g of methyl myristate (Pastel M14, manufactured by Lion Chemical Co., Ltd.) were added and stirred. While stirring, the inside of the autoclave was purged with nitrogen, heated to 100 ° C., and dehydrated under reduced pressure conditions of 1.3 kPa or less for 30 minutes. Next, the temperature was raised to 160 ° C., and 1876 g of ethylene oxide (15 times the total of methyl laurate and methyl myristate) was introduced and stirred under the condition of 0.1 to 0.5 MPa (addition reaction step). Furthermore, after stirring at the addition reaction temperature for 0.5 hour (aging step), the mixture was cooled to 80 ° C. to obtain 2516 g of a crude reaction product (fatty acid methyl ester ethoxylate (MEE), EO average addition mole number = 15). B-2 was obtained by filtering the crude reaction product to remove the catalyst.
The narrow rate of B-2 was 30 mass%.

-B-3: Softanol. 7 to 14 moles of ethylene oxide added to a secondary alcohol having 12 to 14 carbon atoms. Softanol 70 (trade name), manufactured by Nippon Shokubai Co., Ltd. In the general formula (VI), R ⁴ = a branched alkyl group having 12 to 14 carbon atoms, v = 7, w = 0, and x = 0.

B-4: polyoxyethylene alkyl ether. A product obtained by adding 15 moles of ethylene oxide to a natural alcohol (primary alcohol) having 12 and 14 carbon atoms.
[Synthesis Method of Polyoxyethylene Alkyl Ether]
CO-1214 (trade name, natural alcohols having 12 and 14 carbon atoms) manufactured by Procter & Gamble Co., Ltd. and 244.4 g of a 30% by mass NaOH aqueous solution were charged in a pressure-resistant reaction vessel, and the reaction vessel The inside was replaced with nitrogen. Next, after dehydrating for 30 minutes at a temperature of 100 ° C. and a pressure of 2.0 kPa or less, the temperature was raised to 160 ° C. Next, while stirring the reaction solution, 760.6 g of ethylene oxide (gaseous) was gradually added to the reaction solution. At this time, ethylene oxide was added through the blowing tube while adjusting the addition rate so that the reaction temperature did not exceed 180 ° C.
After completion of the addition of ethylene oxide, aging was performed at a temperature of 180 ° C. and a pressure of 0.3 MPa or less for 30 minutes, and then unreacted ethylene oxide was distilled off at a temperature of 180 ° C. and a pressure of 6.0 kPa or less for 10 minutes.
Next, after cooling the temperature to 100 ° C. or lower, 70% by mass p-toluenesulfonic acid was added to neutralize so that the pH of the 1% by mass aqueous solution of the reaction product was about 7, to obtain B-4. It was.

-B-5: EP nonion. Block addition of 8 moles of ethylene oxide, 2 moles of propylene oxide, and 8 moles of ethylene oxide to natural alcohol (mass ratio primary alcohol with 12 carbon atoms / primary alcohol with 14 carbon atoms = 7/3) Nonionic surfactant obtained.

-B-6: AES. Polyoxyalkylene alkyl ether sulfate (mixture of sodium polyoxyethylene lauryl ether sulfate and sodium polyoxyethylene myristyl ether sulfate, average addition mole number of EO 1). In formula (IV), R ⁴⁰ = a linear alkyl group having 12 and 14 carbon atoms, m = 1.0, n = 0, M = sodium, m = 0 with respect to the whole B-6, n = 0 Ratio of compound (component (b0)) = 43% by mass.

[Preparation Example of B-6]
In an autoclave with a capacity of 4 L, 400 g of a trade name CO1270 alcohol (mixture of 75/25 mass ratio of 12-carbon alcohol and 14-carbon alcohol) manufactured by P & G as raw material alcohol and potassium hydroxide as a reaction catalyst After charging 0.8 g of the catalyst and replacing the inside of the autoclave with nitrogen, the temperature was raised with stirring. Subsequently, while maintaining the temperature at 180 ° C. and the pressure at 0.3 MPa or less, 91 g of ethylene oxide was introduced and reacted to obtain an alcohol ethoxylate.
Gas chromatograph mass spectrometer: GC-5890 manufactured by Hewlett-Packard, detector: flame ionization detector (FID), column: Ultra-1 (manufactured by HP, L25m × φ0.2mm × T0.11 μm The alcohol ethoxylate thus obtained had an average addition mole number of ethylene oxide of 1.0. Further, the amount of the compound to which ethylene oxide was not added (final component (b0)) was 43% by mass with respect to the total alcohol ethoxylate obtained.
Next, 237 g of the alcohol ethoxylate obtained above was placed in a 500 mL flask equipped with a stirrer and replaced with nitrogen, and 96 g of liquid sulfuric anhydride (sulfane) was slowly added dropwise while maintaining the reaction temperature at 40 ° C. After completion of dropping, stirring was continued for 1 hour (sulfation reaction) to obtain polyoxyethylene alkyl ether sulfuric acid. Next, this was neutralized with an aqueous sodium hydroxide solution to obtain B-6.

-B-7: AEPS. Monoethanolamine salt of polyoxyethylene polyoxypropane-1,2-diyl alkyl ether sulfate. R ⁴⁰ in the general formula (IV) = a linear alkyl group having 12 carbon atoms, m = 2.0, n = 1.0, M = monoethanolamine.

[Method of synthesizing AEPS]
In an autoclave equipped with a stirrer, a temperature control device and an automatic introduction device, a linear primary alcohol having 12 carbon atoms [manufactured by Tokyo Chemical Industry Co., Ltd., trade name: 1-dodecanol (molecular weight 186.33), purity > 99%] 640 g and KOH 1.0 g were charged and dehydrated at 110 ° C. and 1.3 kPa for 30 minutes. After dehydration, nitrogen substitution was performed, and after heating up to 120 ° C., 199 g of propane-1,2-diyl oxide was charged. Subsequently, after addition reaction and aging at 120 ° C., the temperature was raised to 145 ° C., and 303 g of ethylene oxide was charged. Subsequently, after addition reaction and aging at 145 ° C., the mixture was cooled to 80 ° C., and unreacted ethylene oxide was removed at 4.0 kPa. After removing unreacted ethylene oxide, 1.0 g of acetic acid was added to the autoclave, and the mixture was stirred at 80 ° C. for 30 minutes and then extracted. The alkyl group was dodecyl group, the average added mole number of PO was 1.0, EO An alkoxylate having an average added mole number of 2.0 was obtained.
The resulting alkoxylate was sulfated in a falling film reactor using SO ₃ gas. The obtained sulfate was neutralized with monoethanolamine to obtain a composition containing a monoethanolamine salt (AEPS) of polyoxyethylene polyoxypropane-1,2-diylalkyl ether sulfate.

-B-8: LAS. Linear alkylbenzene sulfonic acid. Lipon LH-200 (trade name), manufactured by Lion Corporation.
-B-9: Palm fatty acid. Anionic surfactant. Product name "coconut fatty acid" (NOF Corporation).
B-10: alkyl chloride (carbon number 12) trimethylammonium. Product name “Arcade 12-37W” manufactured by Lion Akzo.
B-11: Amidoamine. Product name: Katchinal MPAS-R, manufactured by Toho Chemical Co., Ltd.

<C component>
C-1: Polyethyleneimine ethylene oxide adduct. Product name “Sokalan HP20” manufactured by BASF. In the above formula (II-a), compounds wherein R ³² is an ethylene group and m is 20.

<Other optional components>
Coronase: Coronase 48L (trade name), manufactured by Novozymes.
Alcalase: Alcalase 2.5L (trade name), manufactured by Novozymes
MEA: monoethanolamine (alkali agent), trade name “monoethanolamine”, manufactured by Nippon Shokubai Co., Ltd.
BHT: dibutylhydroxytoluene (antioxidant), trade name “SUMILZER BHT-R”, manufactured by Sumitomo Chemical Co., Ltd.
-Butyl carbitol: Butyl carbitol (Nippon Emulsifier Co., Ltd., "butyl diglycol").
Polyethylene glycol: PEG # 1000-L60 (trade name), manufactured by Lion Corporation.
-PG: Propylene glycol, manufactured by BASF.
-Ethanol: Water miscible organic solvent, trade name "specific alcohol 95 degree synthesis", manufactured by Nippon Alcohol Sales Co., Ltd.
-Sodium benzoate: antiseptic, trade name "sodium benzoate" (Toagosei).
・ Calcium chloride: Enzyme stabilizer, trade name “Calcium chloride” (Kanto Chemical).
Sodium lactate: enzyme stabilizer, trade name “sodium lactate” (Kanto Chemical).
-Fragrance | flavor: Fragrance composition A of the fragrance | flavor composition A of Tables 11-18 of Unexamined-Japanese-Patent No. 2002-146399.
-Dye: Colorant, trade name "Green No. 3", manufactured by Sakai Kasei Co., Ltd.
-Water: Distilled water, manufactured by Kanto Chemical Co., Inc.

(Examples 1-12, Comparative Examples 1-6)
[Manufacture of liquid detergent for clothing]
According to the composition shown in Tables 1 and 2, the components (A) to (C) and optional components were added to water and mixed to produce liquid detergents of Examples 1 to 12.
Moreover, the liquid cleaning agent of Comparative Examples 1-6 was manufactured like Example 1 except not having added (C) component or (A) component.
Tables 1 and 2 show the compositions (formulation components, content (mass%)) of the liquid detergents of each example produced.
In the table, when there is a blank blending component, the blending component is not blended.
In the table, the content of the compounding component indicates a pure equivalent amount. However, an enzyme shows content as an enzyme formulation.
“Balance” indicating the content of distilled water means the balance added so that the total amount (% by mass) of all the components included in the liquid detergent is 100% by mass.

  About the liquid cleaning agent of each example, the cleaning power with respect to the oil-based ink stain | pollution | contamination adhering to to-be-washed | cleaned material and liquid stability were evaluated as follows. The evaluation results are shown in Tables 1-2.

[Ink stain cleaning power]
Cotton cloth was put into a fully automatic electric washing machine (AW-80VC, manufactured by Toshiba Corporation), and the bath ratio was adjusted to 20 times. Thereto, 12 g of the liquid cleaning agent of each example was added, and a washing operation was performed in which washing, rinsing, and dehydration were sequentially performed in a standard course. The washing time, rinsing, dehydration, and water volume (set to 36 L) were not adjusted at all and the standard settings of the washing machine were used. The temperature of the tap water used was 15 ° C. This preliminary washing operation was repeated twice or five times. After finishing the pre-washing twice or five times, the cotton cloth was dried overnight by flat laying, and the cotton cloth after drying was cut into 5 × 5 cm to obtain a cotton cloth for evaluation.

An oil-based ballpoint pen (manufactured by ZEBRA, trade name “Clip-on-Slim oil-based ballpoint pen”) was applied to the evaluation cloth to prepare an ink-stained cloth with oil-based ink stains attached thereto. At this time, oil-based ink was applied to the center of the cotton cloth so as to form a circle having a diameter of 2 cm.
This ink soiled cloth was washed by the following procedure.
Apply 0.05 mL of the liquid cleaning agent in each example to the ink stain cloth so that the oil-based ink stain attached to the stain cloth becomes the center, and leave it for 3 minutes. On the other hand, it was cleaned using a washing liquid in which 6 mL of the liquid cleaning agent of each example was dissolved.
As a cleaning tester, Terg-O-Tometer (manufactured by UNITED STATES TESTING) was used. After applying the liquid cleaning agent of each example and leaving it to stand for 3 minutes, the above-mentioned ink stain cloth and the washing liquid are put into a cleaning tester, and the bath ratio is set to 30 times. Washed for minutes. Next, it was transferred to a two-tank washing machine (manufactured by Mitsubishi Electric Corporation, product number: CW-C30A1-H1), dehydrated for 1 minute, rinsed in 30 L of tap water (15 ° C., 4 ° DH) for 3 minutes, and air-dried.

The reflectance was measured with a color difference meter (product name: SE200 type) manufactured by Nippon Denshoku Co., Ltd. for each of the evaluation cloth without ink stain, the ink dirt cloth before washing, and the ink dirt cloth after washing. The washing rate (%) was calculated by the following formula. The cleaning rate (%) was calculated for 10 ink-stained cloths, and the average value was used to evaluate the cleaning power against ink stains based on the following criteria.
Washing rate (%) = 100 × (K / S of ink dirt cloth before washing−K / S of ink dirt cloth after washing) / (K / S of ink dirt cloth before washing−Evaluation cloth) K / S) × 100.
However, K / S is a value obtained by the formula: (1-R / 100) ² / (2R / 100), and R is an evaluation cloth, an ink dirt cloth before washing, or an ink dirt after washing. This is the reflectance (%) of the cloth.
A liquid cleaning agent having a cleaning rate of 50% or more based on the above criteria was regarded as acceptable.

<Evaluation of liquid stability>
A transparent glass bottle (wide-mouth bottle, PS-NO.11) was filled with 100 mL of the liquid cleaning agent of each example, and the lid was closed and sealed. In this state, it was stored in a constant temperature bath at 5 ° C. or 25 ° C. for 7 days.
After such storage, the appearance of the liquid was visually observed, and the appearance stability of the liquid detergent of each example was evaluated according to the following evaluation criteria.
(Evaluation criteria)
○: Precipitated material is not observed at the bottom of the glass bottle, and the fluidity of the liquid is present.
Δ: Precipitated material is observed at the bottom of the glass bottle, but when the glass bottle is shaken lightly, the precipitated material disappears (dissolves).
X: A precipitated substance was observed at the bottom of the glass bottle, and the precipitated substance did not disappear even if the glass bottle was shaken lightly, or gelled or became cloudy immediately after the production of the liquid detergent.
The evaluation results are shown in the columns of room temperature stability (25 ° C.) and low temperature stability (5 ° C.) in Tables 1 and 2, respectively.

  From the results shown in Table 1, it is clear that the liquid detergents of Examples 1 to 12 containing the component (A) and the component (C) have an excellent detergency against ink stains. The liquid detergents of Examples 1 to 5 containing PPG represented by the above formula (III) as the component (A) have a good balance between detergency and liquid stability. In particular, the molecular weight of PPG is 4000 to 5000. The cleaning power against ink stains of the liquid cleaning agents of Examples 3 to 5 is excellent.

  In addition, when comparing the ink stain cleaning power of the evaluation cotton fabrics that differ in the number of times of cleaning before the ink stains are adhered, the cleaning power of the case of cleaning 5 times in advance is more than the case of cleaning twice in advance. Are better. From this, it is understood that the washing power against oily stains such as ink adhered thereafter is improved by repeatedly washing the garment daily using the liquid detergent of the present invention.

On the other hand, it is clear that Comparative Examples 1 to 5 not including the component (C) and Comparative Example 6 not including the component (A) have low detergency against ink stains.
From the above results, it was confirmed that the liquid cleaning agent of the present invention containing the components (A) to (C) had excellent cleaning power against liquid stains such as ink stains and liquid stability.

Claims (4)

(A) component: propylene oxide adduct of alcohol,
(B) component: surfactant,
Component (C): at least one selected from an alkylene oxide adduct (c1) of a polyalkyleneimine and an alkylene oxide adduct (c2) of a polyalkyleneamine;
A liquid cleaning agent for clothing, comprising: The liquid detergent for clothes according to claim 1, wherein the mass ratio (A / C) of the component (A) to the component (C) is 0.1 to 4. The liquid cleaning agent for clothes according to claim 1 or 2, wherein the mass ratio (B / A) of the component (B) to the component (A) is 5 to 90. (B) component contains a nonionic surfactant and an anionic surfactant,
The liquid detergent for clothes according to any one of claims 1 to 3, wherein the content of the nonionic surfactant is greater than that of the anionic surfactant.