JP3987028B2 - Liquid detergent composition - Google Patents

Description

  The present invention relates to a liquid cleaning composition, and more particularly to a liquid cleaning composition suitable for cleaning hard surfaces such as kitchen surroundings, tableware and cooking utensils.

Many dishwashing detergents use an anionic surfactant as a main component as a surfactant from the viewpoint of detergency. In addition, amine oxide type surfactants, amphoteric surfactants, and alkanolamide type surfactants are generally used in combination with anionic surfactants as foaming agents. Furthermore, many liquid detergents containing an alkylene oxide adduct of polyalkylene glycol or polyhydric alcohol are also known. (Patent Documents 1 to 11)
On the other hand, techniques using alkyl glyceryl ether for liquid detergents are known (Patent Documents 12 to 14), and alkylglycoside surfactants are also widely used for liquid detergents (Patent Documents 15 to 19). Polyoxyalkylene type nonionic surfactants are also commonly used surfactants. (Patent Documents 20 to 24)
Japanese Patent No. 2582626 Japanese Patent Laid-Open No. 10-140182 JP-A-10-176184 JP-A-6-17088 JP-A-6-17095 Japanese Patent No. 2526102 Japanese Patent No. 2530215 No. 2618311 Japanese Patent No. 3067541 Japanese Examined Patent Publication No. 3-57158 Japanese National Patent Publication No. 11-513067 JP 2001-19993 A JP 2001-49291 A JP 11-310792 A JP-T 8-502540 Japanese National Patent Publication No. 8-502310 Japanese National Patent Publication No. 8-501817 JP-A-5-148494 JP 2000-26889 A Japanese Patent Application Laid-Open No. 2002-226887 Japanese Patent Application Laid-Open No. 7-188697 JP-A-6-116587 JP-T 8-502540 JP 2003-13092 A

  Liquid detergent compositions such as dishwashing detergents are required to have foaming properties and foam retention properties during washing. For the purpose of solving these problems, amine oxide surfactants should be used in combination as foaming agents. Is preferred. Amine oxide improves not only the foam properties but also the detergency when used in combination with an anionic surfactant. This is because amine oxide has a cationic property in the middle and acidic regions, so it forms an ionic complex with the anion of the anionic surfactant, thereby improving the emulsifying power to oil, resulting in washing It seems that power improves.

  In recent years, concentrated liquid cleaning agents that have been made compact by increasing the concentration of the surfactant have been favored and used. In spite of this tendency to concentrate, the use of dishwashing detergents has become more common than before, in which the detergent is applied directly to the sponge and washed. It is easy to come into contact with a high concentration of surfactant.

  The contact between the high concentration of the surfactant and the hard surface facilitates the removal of oil stains adhering to the hard surface, while the excess surfactant causes sliminess, especially during rinsing. The luster is felt between a body such as a finger or a palm and the surface to be cleaned, and is a feeling that the cleaning agent is present as a smooth surface to be cleaned as an oil film. Basically, it can be resolved by rinsing thoroughly (making the rinsing time longer than the normal rinsing time), but the sensation of wiping that cannot be wiped off during rinsing is not preferable. This also leads to wasted rinsing water.

  The sliminess becomes more prominent when an amine oxide type surfactant is used. The cause is that the amidoxide-type surfactant itself exhibits a property that it is easy to become slippery as compared with other surfactants, but it is presumed that the formation of the complex also has an influence. Although reducing the amount of amine oxide surfactant improves rinsing during rinsing, the foaming properties are impaired, so there is a need for a liquid detergent that satisfies both foaming properties and improvement in rinsing. ing. Further, the combined use of an anionic surfactant and the above-mentioned foaming agent improves the foaming property. However, for example, when many dishes are washed, the foaming property gradually deteriorates.

  The problem to be solved by the present invention is to provide a liquid detergent composition which has good foamability and foam persistence and improves the wetness during washing and rinsing.

As a means for solving the problems, the present invention
(A) 0.1 to 10% by mass of a compound of the following general formula (1),
(B) 5 to 50% by mass of an anionic surfactant having a hydrocarbon group having 10 to 18 carbon atoms,
(C) 0.1 to 30% by mass of a surfactant selected from amine oxide surfactants having a hydrocarbon group having 8 to 18 carbon atoms, amphoteric surfactants, and alkanolamide surfactants,
(D) 0.1 to 10% by mass of one or more selected from (d-1) polypropylene glycol and / or (d-2) an alkylene (carbon number 2 or 3) oxide adduct of a tri- to hexavalent alcohol,
And a liquid detergent composition containing water.

R ^1a -A-B (1)
[Wherein, R ^1a is a C 7-10 alkyl group having one or more tertiary carbons or quaternary carbons, and A is a group selected from —O—, —COO—, and —CONH—. B is a group having 3 to 12 carbon atoms having 2 to 10 hydroxyl groups, or-(R ^1b O) _a -H (where R ^1b is an alkylene group having 2 or 3 carbon atoms, and a is It is an average added mole number and represents a number of 1 to 5). ]

  The liquid detergent composition of the present invention has good foaming and foam persistence, suppresses sliminess during washing of dishes, cooking utensils, etc., and easily removes sliminess during rinsing.

<(A) component>
The component (a) of the present invention is a compound of the general formula (1), which is a compound having a specific branched alkyl group and a specific hydrophilic group.

R ^1a -A-B (1)
[Wherein, R ^1a is a C 7-10 alkyl group having one or more tertiary carbons or quaternary carbons, and A is a group selected from —O—, —COO—, and —CONH—. B is a group having 3 to 12, preferably 3 to 8, carbon atoms having 2 to 10 hydroxyl groups, or — (R ^1b O) _a —H (where R ^1b is an alkylene having 2 or 3 carbon atoms). A is an average addition mole number, and is a group selected from 1 to 5). ]
R ^1a is an alkyl group having a branched structure, preferably a 2-ethylhexyl group, an iso-nonyl group, an iso-decyl group, a residue excluding the carbonyl carbon of the 2-ethylhexanoyl group, or an iso-nonanoyl group. A residue excluding the carbonyl carbon and a group excluding the carbonyl carbon of the iso-decanoyl group are preferable, and a residue excluding the carbonyl carbon of the 2-ethylhexyl group or 2-ethylhexanoyl group is particularly preferable.

A is a group for linking R ^1a and B, and preferably —O—. Specifically, B represents a reducing sugar residue, a reductive aminated sugar residue, a residue excluding one hydroxy group of glycerin, and a residual excluding one hydroxy group of polyglycerin (average polymerization degree 2 to 4). And a group selected from — (C ₂ H ₄ O) _b —H (b is the average number of moles added and represents a number of 2 to 5).

  Specific examples of the compound of the general formula (1) include compounds of the following general formulas (1-1) to (1-4).

R ^1a- (G) _e (1-3)
R ^1a —O— (C ₂ H ₄ O) _f —H (1-4)
[R ^1a has the same meaning as described above.
c is a number of 1 to 4, preferably 1.
d is a number of 1 to 4, preferably 1.
G represents a monosaccharide residue, and e represents an average value of 1 to 5, preferably 1 to 3, particularly preferably 1 to 2.
f shows the number of the average values 2-5. ]
The compound of the general formula (1-1) is produced by reacting 2-ethylhexanol, iso-nonanol, iso-decanol and an epoxy compound such as epihalohydrin or glycidol using an acid catalyst such as BF ₃ or an aluminum catalyst. The method to do is common.

  As the compound of the general formula (1-1), 2-ethylhexyl monoglyceryl ether is preferable, and a method of manufacturing by the above-described manufacturing method is common, and a plurality of methods as described in JP-A-2001-49291 are used. A mixture containing the product.

  Specifically, as 2-ethylhexyl monoglyceryl ether, a compound in which 2-ethylhexanol is added to the 1-position of an epoxy compound [Compound 1; 3- (2-ethylhexyloxy) -1,2-propanediol], an epoxy compound The compound [Compound 2; 2- (2-ethylhexyloxy) -1,3-propanediol] added to the 2-position of can be mentioned. Moreover, as a by-product, a polyaddition compound (compound 3) in which an epoxy compound is further added to the compound 1 or 2 can be exemplified.

  The 2-ethylhexyl monoglyceryl ether preferably has a compound 3 content of 30% by mass or less, more preferably 10% by mass or less, and particularly preferably 1% by mass or less.

  The compound of the general formula (1-2) is an esterification reaction (or ester) of glycerin and preferably 2-ethylhexanoic acid, iso-nonanoic acid, iso-decanoic acid (or their lower alkyl ester, acid chloride). Exchange reaction). However, in this case, a mixture of a monoesterified product, a diesterified product, and a triesterized product is obtained. In the present invention, those having a monoester content in these mixtures of 60 mol% or more, preferably 80 mol% or more are used.

  In the compound of the general formula (1-3), G is a monosaccharide residue, and examples thereof include triose, tetrose, pentose, and hexose having 3 to 6 carbon atoms. Specific examples include apiose, arabinose, galactose, glucose, lyxose, mannose, gulose, aldose, idose, talose, and xylose.

  In the present invention, among these, pentose or hexose having 5 or 6 carbon atoms is particularly preferable, and glucose is most preferable. As G, the above monosaccharides are shown, but oligosaccharides obtained by condensing 2 to 5, preferably 2 or 3, of these monosaccharides may be used for production. Further, a mixture of monosaccharide and oligosaccharide may be used. In this case, the average degree of condensation is 1 to 5, preferably 1 to 3, particularly preferably 1 to 2, and most preferably 1 to 1.5. preferable.

  The compound of the general formula (1-3) is an acetalization reaction or a ketalization reaction of 2-ethylhexanol, iso-nonanol, iso-decanol and the reducing end of the monosaccharide or oligosaccharide using an acid catalyst. Can be easily synthesized.

The compound of the general formula (1-4) is obtained by reacting 2-ethylhexanol, iso-nonanol, or iso-decanol with ethylene oxide at an alcohol / alkylene oxide molar ratio of 1/2 to 1/5. It is a mixture of compounds having a reaction alcohol containing f of about 0 to 10. In particular, a compound having an average value of f containing 2 to 5 containing unreacted alcohol is preferred. The average value is used H ¹ -NMR, it is possible to easily obtain the integral value of the proton of proton and the oxyethylene groups α-position of the R ^1a. These may be used after removing unreacted alcohol (compound with f = 0) and compounds with f> 5 or more by performing an operation such as distillation.

  In the compound of the general formula (1) of the present invention, it is preferable that the content of unreacted alcohol or fatty acid is small in order to obtain the effects of the present invention. The content of the unreacted alcohol or fatty acid in the compound of the general formula (1) is preferably 10% by mass or less, more preferably 5% by mass or less, still more preferably 3% by mass or less, and most preferably 1% by mass or less. is there.

As the component (a), particularly in the compound of the general formula (1-1), R ^1a is a 2-ethylhexyl group, and in the compound of c = 1, and in the compound of the general formula (1-3), R ^1a is 2- A compound having an ethylhexyl group and G being glucose is preferred, and a compound of formula (1-1) in which R ^1a is a 2-ethylhexyl group and c = 1 is most preferred.

<(B) component>
The component (b) of the present invention is an anionic surfactant having a hydrocarbon group having 10 to 18 carbon atoms, and preferred specific examples thereof include alkylbenzenesulfonic acid having an alkyl group having 10 to 15 carbon atoms or a salt thereof, C10-16 monoalkyl sulfate ester salt, polyoxyalkylene alkyl ether sulfate having an alkyl group having 10-16 carbon atoms and an average of 1.0-4.0 mol of oxyalkylene groups having 2 or 3 carbon atoms added Examples thereof include ester salts, α-olefin sulfonates having 8 to 16 carbon atoms, and α-sulfo fatty acids (8 to 16 carbon atoms) lower alkyl (1 to 3 carbon atoms) ester salts. Examples of the salt include sodium salt, potassium salt, magnesium salt, and alkanolamine salt, and sodium salt, potassium salt, and magnesium salt are particularly preferable from the viewpoint of viscosity.

  In the present invention, an alkyl group having 10 to 14 carbon atoms in particular and an oxyalkylene group having 2 or 3 carbon atoms, preferably an oxyethylene group, is on average 1.0 to 3.0 mol, particularly preferably 1.5 to It is preferable to use 3.0 mol added polyoxyalkylene alkyl ether sulfate salt, preferably sodium salt, potassium salt, or magnesium salt from the viewpoint of cleaning effect, and contains a high concentration of anionic surfactant. This is preferable because the storage stability of the composition at low or high temperatures can be improved.

  When a polyoxyalkylene alkyl ether sulfate salt is used as the component (b), a polyoxyalkylene alkyl ether having a branched primary alkyl group produced from an alcohol obtained by hydroformylating a linear 1-alkene as a raw material Sulfuric acid ester salts are preferred. Here, hydroformylation is a method for obtaining an alcohol by adding carbon monoxide to a linear 1-alkene using a carbonyl complex such as iron, cobalt or nickel as a catalyst. An alcohol containing groups is obtained.

  The polyoxyalkylene alkyl ether sulfate ester salt further adds an alkylene oxide, preferably propylene oxide (hereinafter referred to as PO) or ethylene oxide (hereinafter referred to as EO), more preferably EO, to such an alcohol, Further, it can be obtained by sulfonation with sulfur trioxide or chlorosulfonic acid and neutralization with an alkali agent. The average number of added moles is preferably 1.0 to 3.0, more preferably 1.5 to 3.0, and particularly preferably 1.5 to 2.5 from the viewpoint of the cleaning effect. As the alkali agent used for neutralization, sodium hydroxide, potassium hydroxide, magnesium hydroxide, sodium carbonate, potassium carbonate, and magnesium carbonate are preferable, and sodium hydroxide, potassium hydroxide, and magnesium hydroxide are more preferable.

  The polyoxyalkylene alkyl ether sulfate salt thus obtained contains a branched alkyl group, and the mass ratio of the polyoxyalkylene branched alkyl ether sulfate salt to the total polyoxyalkylene alkyl ether sulfate salt is 5-80 mass%, Furthermore, 10-70 mass% is preferable in order to achieve the outstanding cleaning effect.

  In particular, when the polyoxyalkylene alkyl ether sulfate salt is blended in the composition in an amount exceeding 10% by mass (for example, when blended at a concentration of 15 to 40% by mass), in the polyoxyalkylene alkyl ether sulfate salt The content of the polyoxyalkylene branched alkyl ether sulfate ester salt preferably satisfies the above content range. The polyoxyalkylene alkyl ether sulfate salt itself has a characteristic that it is less sticky than other surfactants, but it increases with the increase in concentration as it increases with the use of amine oxide surfactants. Since it tends to remain on the surface to be cleaned due to viscosity or gelation, there is concern about an increase in the feeling of sliminess, but satisfying the content range of the branched chain described above is preferable because the feeling of sliminess is reduced. .

<(C) component>
The component (c) of the present invention is a surfactant selected from amine oxide surfactants having a hydrocarbon group having 8 to 18 carbon atoms, amphoteric surfactants, and alkanolamide surfactants. Examples of the compound include compounds represented by the following general formulas (2) to (4).

[Wherein, R ^2a is an alkyl group or alkenyl group having 8 to 16 carbon atoms, R ^2b is an alkylene group having 1 to 6 carbon atoms, and D is —COO—, —CONH—, —OCO—, — It is a group selected from NHCO-. g is a number of 0 or 1, and R ^2c and R ^2d are each an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group. ]

[Wherein, R ^3a is an alkyl group or alkenyl group having 9 to 17 carbon atoms, and R ^3b is an alkylene group having 1 to 6 carbon atoms. E is a group selected from —COO—, —CONH—, —OCO—, —NHCO—, and —O—, and h is a number of 0 or 1. R ^3c and R ^3d are each an alkyl group having 1 to 3 carbon atoms or a hydroxyalkyl group, and R ^3e is an alkylene group having 1 to 5 carbon atoms which may be substituted with a hydroxy group. F is a group selected from —SO ₃ ^— , —OSO ₃ ^— , and —COO ^— . ]

[Wherein, R ^4a —CO— represents a saturated or unsaturated acyl group having 8 to 20 carbon atoms, and R ^4b represents a methyl group, an ethyl group, or — (C ₂ H ₄ O) _i —H. R ^4c is — (C ₂ H ₄ O) _j —H. i and j are each a number of 0 to 5, and i + j is 1 to 6. ]
In the general formula (2), R ^2a is preferably an alkyl group or alkenyl group having 10 to 14 carbon atoms, and particularly preferably a lauryl group (or lauric acid residue) and / or a myristyl group (or myristic acid residue). ). D is preferably —COO— or —CONH—, and most preferably —CONH—. R ^2b preferably has 2 or 3 carbon atoms, and R ^2c and R ^2d are preferably methyl groups.

In the present invention, R ^2a may be a single alkyl (or alkenyl) chain length or a mixed alkyl group (or alkenyl group) having different alkyl (or alkenyl) chain lengths. In the latter case, those having a mixed alkyl (or alkenyl) chain length derived from a vegetable oil selected from coconut oil and palm kernel oil are preferred. Specifically, the cleaning effect is such that the molar ratio of lauryl group (or lauric acid residue) / myristyl group (or myristic acid residue) is 95/5 to 20/80, preferably 90/10 to 30/70. And from the viewpoint of foaming property.

In the general formula (3), R ^3a is preferably an alkyl group having 9 to 15 carbon atoms, particularly 9 to 13 carbon atoms, and R ^3b is preferably an alkylene group having 2 or 3 carbon atoms. E is preferably -CONH-. R ^3c and R ^3d are preferably a methyl group or a hydroxyethyl group. F is -SO ₃ ^-, or -COO ^- are preferred, F is -SO ₃ ^- are preferred, F is -COO ^- - ^{R 3e} is _-CH 2 CH (OH) CH ₂ in the case of the case of R ^3e is preferably a methylene group.

In the compound of the general formula (4), R ^4a —CO— is preferably a saturated or unsaturated acyl group having 8 to 17 carbon atoms. Preferred specific examples are derived from octanoic acid, decanoic acid, dodecanoic acid, tetradecanoic acid, hexadecanoic acid, octadecanoic acid, docosanoic acid, linoleic acid, 2-ethylhexanoic acid, 2-octylundecanoic acid, isostearic acid and oleic acid. Particularly preferred are acyl groups derived from octanoic acid, decanoic acid, dodecanoic acid, tetradecanoic acid, hexadecanoic acid, octadecanoic acid and oleic acid.

In the compound of the general formula (4), R ^4b is a methyl group, an ethyl group or — (C ₂ H ₄ O) _i —H, and preferably a methyl group or a hydrogen atom (i = 0). R ^4c is — (C ₂ H ₄ O) _j —H, and j is preferably a number from 1 to 5, particularly preferably from 1 to 3, from the viewpoint of durability of the cleaning effect.

  Preferable specific examples of the compound of general formula (4) include general formula (4-1) and general formula (4-2).

[Wherein, R ^4b and j have the same meaning as described above. ]
<(D) component>
As the component (d) of the present invention, either one of the component (d-1) and the component (d-2) is used, or both are used in combination.

The component (d-1) is polypropylene glycol, and commercially available products can be used. In the present invention, polypropylene glycol having a number average molecular weight of preferably 300 to 6000, more preferably 400 to 5000, and most preferably 500 to 3000 is suitable.
The component (d-2) is an alkylene (carbon number 2 or 3) oxide adduct of a trivalent to hexavalent alcohol. The number average molecular weight of these adducts is preferably 300 to 10,000, more preferably 400 to 5000, and most preferably 500 to 3000.

  Examples of the trivalent to hexavalent alcohol include glycerin, polyglycerin, trimethylolpropane, pentaerythritol, and sorbitol, and glycerin is particularly suitable. The adduct of component (d-2) can be prepared by adding an alkylene (carbon number 2 or 3) oxide, preferably ethylene oxide, to these alcohols so that an adduct having a number average molecular weight in the above range is obtained. . The number average molecular weight of the component (d) of the present invention can be determined from the hydroxyl value.

  In the present invention, the (d-1) component and / or the (d-2) component is used as the (d) component, preferably by using the (d-1) component and the (d-2) component in combination. The sustainability (foaming property) can be improved. The mechanism by which such an action is expressed is considered as follows.

  Foam formed by the surfactant aqueous solution is a phenomenon that occurs when the surfactant is adsorbed on the gas / liquid interface. Since the liquid in the foam film is drained over time due to gravity, the foam film becomes gradually thinner (that is, the foam film becomes thinner) and eventually breaks. The component (d) present in the liquid in the foam film acts as a resistance against the thinning of the foam film due to its large molecular weight, and the drainage is slowed by increasing the viscosity of the liquid in the foam film. Therefore, it is considered that the foam holding property is improved because the foam film is suppressed from thinning and the foam is difficult to break.

<Other ingredients>
In the present invention, for the purpose of improving the emulsifying power of the component (b) and enhancing the cleaning effect, it is preferable to blend magnesium [hereinafter referred to as the component (e)], and magnesium is present in the system as a salt or a free ion. And may be blended as a counter ion of the component (b) or may be blended as a water-soluble magnesium compound. As a water-soluble magnesium compound, the solubility in water at 20 ° C. in the magnesium compound described in Chemical Handbook II (Revised 3rd Edition), page 166, table 8.42, and page 190, table 8.47 is 1 g / A compound of 100 g or more, preferably 10 g / 100 g or more is suitable. Of these, magnesium sulfate, magnesium chloride, magnesium carbonate, magnesium nitrate, and magnesium acetate are most preferred in the present invention.

  In the present invention, for the purpose of enhancing the detergency, it is preferable to contain a surfactant other than the component (b) and the component (c) [hereinafter referred to as the component (f)], and a nonionic surfactant is used. Is preferred. As a nonionic surfactant preferable as the component (f), a compound represented by the following general formula (5) can be given.

R ^5a —O— (R ^5b O) _k —H (5)
[Wherein, R ^5a is an alkyl group or alkenyl group having 11 to 18 carbon atoms, preferably 11 to 15 carbon atoms, and R ^5b is an alkylene group having 2 or 3 carbon atoms, preferably an ethylene group. k represents a number of 6 to 100, preferably 6 to 20. ]
In the present invention, it is preferable to contain a hydrotrope agent (hereinafter referred to as component (g)) for the purpose of improving storage stability. As the hydrotrope, toluenesulfonic acid, xylenesulfonic acid, cumenesulfonic acid and their sodium, potassium or magnesium salts are preferable, and p-toluenesulfonic acid is particularly preferable.

  In the present invention, a solvent other than the component (a) [hereinafter referred to as the component (h)] can be contained as an object for improving storage stability and as a viscosity modifier. Specific examples of the solvent are preferably water-soluble organic solvents selected from ethanol, isopropyl alcohol, ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, glycerin, isoprene glycol, propylene glycol monomethyl ether, and propylene glycol monoethyl ether.

<Liquid cleaning composition>
The contents of the components (a) to (d) in the liquid detergent composition of the present invention are as follows.

  The content of the component (a) is from 0.1 to 10% by mass, preferably from 0.3 to 7% by mass, more preferably from 0.5 to 5% by mass, from the viewpoint of improving luster during washing and rinsing. It is.

  (B) Content of a component is 5-50 mass% from the point of a cleaning effect, Preferably it is 10-45 mass%, More preferably, it is 10-40 mass%.

  The content of the component (c) is from 0.1 to 30% by mass, preferably from 0.5 to 20% by mass, and more preferably from 1 to 15% by mass, from the viewpoint of foamability and foaming persistence.

  (D) Content of a component is 0.1-10 mass% from the point of foaming sustainability, Preferably it is 0.5-5 mass%, More preferably, it is 0.5-3 mass%.

  The mixing ratio (mass ratio) of the component (d-1) and the component (d-2) (d-2) / (d-1) is preferably 1/9 to 9 from the viewpoint of improving the persistence of foaming. / 1, more preferably 2/8 to 8/2, particularly preferably 3/7 to 7/3.

  In the liquid detergent composition of the present invention, by containing the component (c) and the component (d) together with the component (b), the foam is increased when contacted with water, and the foam is maintained by the action of the component (d). Sexuality is enhanced. As a result, the durability of the cleaning performance is improved, and for example, the number of dirty dishes cleaned by using a certain amount of the composition can be greatly increased.

  And since it contains the component (a), the sliminess between the finger and the object to be cleaned such as a dish is suppressed by the blending effect of the component (a), and further by the blending effect of the component (a), When rinsing, the sliminess is easily removed.

  The contents of components other than the components (a) to (d) in the liquid detergent composition of the present invention are as follows.

  The component (e) is preferable because it can obtain a high cleaning effect due to the interaction with the component (b), and can be used in combination with the component (a) to further reduce sliminess. (E) Content of a component is 0.01-2 mass% as magnesium, More preferably, it is 0.05-1 mass%, Most preferably, it is 0.1-1 mass%. Further, the molar ratio [(b) / (e)] of the component (b) and the component (e) (as magnesium) is preferably 300/1 to 1/1, more preferably 100/1 to 1/1. Most preferably, it is 50/1-2/1.

  The component (f) is preferably contained for the purpose of enhancing the cleaning effect and improving storage stability. In particular, the compound of the general formula (5) is excellent in the above-described improving effect. However, a large amount of blending tends to promote luster when washing dishes, and tends to reduce the effect of component (a). For this reason, the content of the component (f) is preferably 0.1 to 20% by mass, more preferably 0.5 to 15% by mass, and particularly preferably 1.0 to 15% by mass.

  The component (g) is preferably contained from the viewpoint of storage stability, and the content of the component (g) is preferably 0.1 to 10% by mass, more preferably 1 to 10% by mass, and particularly preferably 2%. -6 mass%.

  The component (h) is preferable in terms of improving storage stability, and is also effective as a viscosity modifier. The content of the component (h) is preferably 1 to 20% by mass, more preferably 5 to 20% by mass, and particularly preferably 5 to 15% by mass.

  The composition of the present invention is in a liquid form in which the above-described components are dissolved or dispersed in water, and the content of water is preferably 20 to 60% by mass, more preferably 30 to 30% from the viewpoint of storage stability. 60 mass%, More preferably, it is 40-60 mass%, Most preferably, it is 45-55 mass%.

  The pH at 20 ° C. of the composition of the present invention is preferably 6 to 8, more preferably 6.5 to 7.5, from the viewpoint of storage stability and safety to the skin.

  Examples of pH adjusters include inorganic acids such as hydrochloric acid and sulfuric acid, acid agents such as citric acid, succinic acid, malic acid, fumaric acid, tartaric acid, malonic acid, and maleic acid, and sodium hydroxide and hydroxide. Preferably, alkali agents such as potassium carbonate, ammonia and derivatives thereof, amine salts such as monoethanolamine, diethanolamine, and triethanolamine are used alone or in combination, such as sodium carbonate and potassium carbonate, particularly from hydrochloric acid, sulfuric acid, and citric acid. It is preferable to use an acid selected and an alkali agent selected from sodium hydroxide and potassium hydroxide. Any compound is blended within a range that does not have a great influence on the viscosity characteristics.

  From the viewpoint of ease of use, the composition of the present invention has a viscosity at 20 ° C. of preferably 10 to 1000 mPa · s, more preferably 30 to 700 mPa · s, and particularly preferably 50 to 500 mPa · s. Such a viscosity range can be adjusted using, for example, the above-described component (g), component (h), and the like.

  The viscosity as used in the present invention is measured as follows. First, a B-type viscometer model BM manufactured by TOKIMEC. INC is provided with a rotor of rotor number No. 2. The sample is filled in a tall beaker and adjusted to 20 ° C. in a thermostatic bath. A sample adjusted to a constant temperature is set in a viscometer. The rotational speed of the rotor is set to 60 r / m, and the viscosity 60 seconds after the start of rotation is taken as the viscosity of the present invention.

  As other components, as long as the viscosity characteristics are not affected, components usually blended in a liquid detergent such as a fragrance component, a sterilizing component, a preservative, a turbidity agent, and a colorant can be blended.

  The liquid detergent composition of the present invention is suitable as a liquid detergent composition for hard surfaces (particularly for kitchens) such as washing dishes, cooking utensils, and kitchenware.

  The liquid cleaning composition of the present invention is a foaming property in a method in which a liquid is soaked in a flexible material such as sponge (preferably containing water) and directly brought into contact with a hard surface such as tableware or cooking utensils. In addition, it is excellent in persistence of foam, can suppress the sliminess of dishes and cooking utensils during washing, and can quickly remove the sliminess during rinsing.

  A liquid detergent composition was prepared using the components shown in Tables 1 and 3. The foaming property, feel, and detergency of these compositions were evaluated by the following methods. The results are shown in Table 1. Table 2 shows an example of blending a kitchen liquid detergent composition having the effects of the present invention.

<Measurement of foamability>
A commercially available new sponge (flexible absorber, Kikuron) is rinsed with tap water and squeezed until the content of tap water becomes 10 g. 30 g of a 1% by weight aqueous solution of the composition of Table 1 is soaked in a sponge and placed on a ceramic dish. Place a plastic plate the same size as the sponge on the sponge and compress the plastic plate twice by hand. The foam from the sponge is collected in a measuring cylinder and the volume (ml) of the foam is measured.

<Foam persistence>
1 g of model dirt in which 0.1% by weight of pigment (Sudan Red) was uniformly mixed with salad oil was spread evenly on a ceramic dish, and 5 g of tap water was placed on it as model contaminated tableware.

  After washing a commercially available new sponge (flexible absorbent, Kyklon) with tap water and squeezing until the content of tap water is 10 g, soak 1 g of the composition in Table 1 and 30 g of tap water. It was. After the sponge is bubbled 3 times on the model contaminated tableware, the model contaminated tableware is scrubbed 5 times in a circular pattern, and the sponge is swirled once on the plate, and then a circle 5 is drawn. Washed twice. At this time, foam was prevented from spilling from the dish. Ten dishes were washed by the same operation, all the foam on each dish was collected in a measuring cylinder, and the volume (ml) of foam was measured.

<Feel evaluation>
1 g of model oil stain in which 0.1% by weight of pigment (Sudan Red) was uniformly mixed with salad oil was spread evenly on a ceramic plate, and 5 g of tap water was placed on the dish to make a model contaminated tableware.

  A commercially available new sponge (flexible absorber, Kikuron) is rinsed with tap water and squeezed until the tap water content is 10 g, and then impregnated with 1 g of the composition shown in Table 1 and 20 g of tap water. After the sponge was foamed by hand on the model-contaminated tableware 2 to 3 times, 5 model-contaminated tableware were scrubbed, and the wetness during the washing was subjected to sensory evaluation based on the following criteria. Next, the model-contaminated tableware that had been washed was rinsed with tap water, and the sensory evaluation was performed based on the following criteria to determine whether it was easy to get wet during rinsing.

[Standard for sliminess during cleaning]
○: Not very slippery.
Δ: Slightly slim.
X: Very slimy.

[Standard for ease of slipping during rinsing]
○: It is possible to get a slimy immediately.
Δ: It takes a little time before the sliminess is removed.
X: It takes time until the sliminess is removed.

<Detergency test>
1 g of model oil stain in which 0.1% by weight of a pigment (stan red) was uniformly mixed with salad oil was spread evenly on a polypropylene plate, and 5 g of tap water was further placed on the model contaminated tableware.

  A commercially available new sponge (flexible absorber, Kikuron) is rinsed with tap water and squeezed until the tap water content is 10 g, and then impregnated with 1 g of the composition shown in Table 1 and 20 g of tap water. After the sponge was bubbled with the hand 2-3 times on the model-contaminated tableware, the model-contaminated tableware was rubbed and the number of dishes that could be washed (confirmed by the disappearance of the color attached to the tableware) was determined.

(Note) The symbols in the table represent the following.
・ PPG (1): Polypropylene glycol (Exenol 1020, manufactured by Asahi Glass Co., Ltd.)
・ PPG (2): Polypropylene glycol (Excenol 3020, manufactured by Asahi Glass Co., Ltd.)
GLY (1): ethylene oxide adduct of glycerin, number average molecular weight 1000
GLY (2): ethylene oxide adduct of glycerin, number average molecular weight 3000
ES-I: Sodium polyoxyethylene alkyl ether sulfate ester [The raw material alcohol is an alcohol obtained by hydroformylation using 1-decene and 1-dodecene 50/50 (mass ratio) as raw materials. After adding an average of 2 moles of EO to this alcohol, it was sulfated with sulfur trioxide and neutralized with sodium hydroxide. The ratio of the total polyoxyethylene branched chain alkyl ether sulfate sodium in the total polyoxyethylene alkyl ether sulfate sodium was 42% by mass.
ES-II: ammonium polyoxyethylene coconut alkyl ether sulfate (EO average addition mole number 2 mol)
ES-III: ammonium polyoxyethylene lauryl ether sulfate (EO average addition mole number 4 mol)
AO-I: N-decyl-N, N-dimethylamine oxide / N-lauryl-N, N-dimethylamine oxide / N-myristyl-N, N-dimethylamine oxide = 25/50/25 (mass ratio)
AO-II: N-lauric acid amidopropyl-N, N-dimethylamine oxide sulfobetaine: N-lauryl-N, N-dimethyl-N- (2-hydroxy-1-sulfopropyl) ammonium sulfobetaine GE- 2EH: 2-ethylhexyl monoglyceryl ether (99% by mass or more of monoglyceryl ether)
GE-isoC5: isoamyl monoglyceryl ether (99% by mass or more of monoglyceryl ether)
GE-C8: n-octyl monoglyceryl ether (99% by mass or more of monoglyceryl ether)
GE-C10: n-decyl monoglyceryl ether (99% by mass or more of monoglyceryl ether)
MG-2EH: 2-ethylhexanoic acid monoglyceride (mixture of diglyceride and triglyceride, monoglyceride content in glyceride is 80%)
AG-2EH: alkyl glycoside whose alkyl group is a 2-ethylhexyl group, the average degree of condensation of glucose is 1.3
EO-2EH: polyethylene glycol 2-ethylhexyl ether, ethylene glycol average addition mole number 4
AG-IN: alkyl glycoside whose alkyl group is an iso-nonyl group, the average degree of condensation of glucose is 1.3
AG-ID: alkylglycoside whose alkyl group is an iso-decyl group, the average condensation degree of glucose is 1.3
Nonion-I: 12- and 13-carbon mixed alkyl secondary alcohol added with an average of 7 mol of EO (Softanol 70H, manufactured by Nippon Shokubai Co., Ltd.)
Nonionic-II: Alkyl glucoside having an alkyl group composition of 12 carbons / 14 carbons = 60/40 (molar ratio) mixed alkyl and an average degree of glucoside condensation of 1.5. P-TS: sodium p-toluenesulfonate -PG: Propylene glycol-Perfume: Perfume ingredients in Table 3-pH: 1N-adjusted with sulfuric acid aqueous solution or 1N-sodium hydroxide.

Claims (2)

(A) 0.1 to 10% by mass of a compound of the following general formula ( 1-1 ),
(B) 5 to 50% by mass of an anionic surfactant having a hydrocarbon group having 10 to 18 carbon atoms,
(C) 0.1 to 30% by mass of a surfactant selected from amine oxide surfactants having a hydrocarbon group having 8 to 18 carbon atoms, amphoteric surfactants, and alkanolamide surfactants,
(D) 0.1 to 10% by mass of one or more selected from (d-1) polypropylene glycol and / or (d-2) an alkylene (carbon number 2 or 3) oxide adduct of a tri- to hexavalent alcohol,
And a liquid detergent composition for hard surfaces containing water.

[Wherein, R ^1a is a C 7-10 alkyl group having one or more tertiary carbons or quaternary carbons, and c is a number of 1-4 . ] 2. The liquid cleaning according to claim 1, wherein in the component (d), the mass ratio (d-2) / (d-1) of the component (d-1) to the component (d-2) is 1/9 to 9/1. Agent composition.