GB2197338A - Liquid detergent composition - Google Patents
Liquid detergent composition Download PDFInfo
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- GB2197338A GB2197338A GB08721893A GB8721893A GB2197338A GB 2197338 A GB2197338 A GB 2197338A GB 08721893 A GB08721893 A GB 08721893A GB 8721893 A GB8721893 A GB 8721893A GB 2197338 A GB2197338 A GB 2197338A
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- alkenyl
- polyoxyalkylene
- detergent composition
- liquid detergent
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/94—Mixtures with anionic, cationic or non-ionic compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/06—Ether- or thioether carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/526—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 are polyalkoxylated
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
A liquid detergent composition comprises in specific proportions, (a) a non-soap anionic surface active agent, (b) a nitrogen-containing amphoteric or non-ionic surface active agent, and (c) a nitrogen-free polyoxyalkylene addition type non-ionic surface active agent with from 50 to 300 moles of oxyalkylenes. The composition exhibits mildness, detergency and foaming ability at a low concentration of less than 1% for washing dishes and tableware.
Description
SPECIFICATION
Liquid detergent composition
This invention relates to a liquid detergent possessing an excellent detergency and abundant foaming ability. The detergent is particularly suitable for use in washing dishes and other tablewares.
Detergency and foaming ability are the most basic properties which a household detergent composition is supposed to possess. It is commonly accepted that there are no special relations between the foaming ability and detergency. Thus, a detergent possessing an excellent detergency is not necessarily one possessing a good foaming ability.
Most consumers, however, very frequently relate detergency with foaming ability, and tend to favor a detergent that produces abundant foam. For this reason, a detergent possessing both excellent detergency and foaming ability is favored as a commodity.
Conventional detergent compositions comprise an anionic surface active agent as a major detergent component, primarily for affording foaming ability, and a nitrogen-containing amphoteric or non-ionic surface active agent such as tert-amine oxides, higher fatty acid alkanol amides and alkyl betains, for imparting detergency or supplementing the foaming ability when they are used to wash out oily stains.
Although conventional detergents using an anionic surface active agent and a nitrogen-containing amphoteric or non-ionic surface active agent in combination exhibit detergency and foaming ability of a certain level at a relatively high concentration of more than 1%; at a lower concentration, i.e. at less than 1%, their detergency for oily stains is deficient, and moreover the stains once removed, tend to attach again to the object being washed.
In recent years, consumers have become inclined to use detergents at a lower concentration in order to prevent their hands from getting roughened. A lower concentration is also favorable from the economical point of view.
There has been therefore a strong desire for the development of a liquid detergent exhibiting an excellent detergency and foaming ability at a low concentration.
The inventors have made extensive studies to resolve these problems in conventional detergents, and as a result, it was found that a liquid detergent composition exhibiting an excellent detergency and foaming ability at a low concentration, e.g. at less than 1%, could be obtained by adding a specific polyoxyalkylene addition type non-ionic surface active agent to a detergent composition containing an anionic surface active agent and a nitrogen-containing amphoteric or non-ionic surface active agent in combination. Such a finding has led to the completion of this invention.
Accordingly, an object of this invention is to provide a liquid detergent composition comprising: (A) from 10 to 40% by weight of a synthesized anionic surface active agent, (B) from 1 to 10% by weight of a nitrogen-containing amphoteric or non-ionic surface active agent, and (C) from 0.5 to 10% by weight of a nitrogen-free polyoxyalkylene addition type non-ionic surface active agent having from 50 to 300 oxyalkylene groups per molecule.
DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
The component (A) to be used in the composition of this invention include polyoxyethylene alkyl- or alkenyl ether sulfates, alkylbenzenesulfonates, polyoxyethylene alkyl- or alkenyl ether acetates, a-olefin sulfonates, alkane sulfonates, salts of xx-sulfofatty acid esters, and the like.
Among these compounds, polyoxyethylene alkyl- or alkenyl sulfates are preferable in view of mildness to the skin and alkylbenzenesulfonates are preferable in view of detergency and cost.
More specific examples of these preferable synthesized anionic surface active agents may be illustrated as follows.
Polyoxyethylene alkyl- or alkenyl ether sulfates may be the compounds represented by the following formula (I): R,O(CH2CH20)aSO3M 11) in which R, represents an alkyl- or alkenyl group having from 10 to 24 carbon atoms, a is a value of from 1 to 5, M represents an alkali metal, ammonium or an alkanolamine group.
Aikylbenzenesulfonates may be the compounds represented by the following formula (ill):
in which R2 represents an alkyl group having from 8 to 20 carbon atoms and M has the same meaning as defined above.
Polyoxyethylene alkyl- or alkenyl ether acetates may be the compounds represented by the following formula (III): R,O(CH2CH20)aCH2COOM (III) in which R1, a and M each has the same meaning as defined above.
Salts of a-olefin sulfonic acid and alkane sulfonic acid may be those compounds having from 10 to 24 carbon atoms, and salts of a-sulfofatty acid esters may be those compounds which are derived from fatty acids having from 10 to 24 carbon atoms.
Although there is no specific limitation to the Component (B), the nitrogen-containing non-ionic or amphoteric surface active agent, so long as the same has a good solubility with the above component (A) to be employed, preferable compounds are mono long chained alkyl- or alkenyl tert-amine oxides, or higher fatty acid alkanol amides or ethylene oxide adducts thereof.Mono long chained alkyl- or alkenyl tert-amine oxides may be, for example, the compounds represented by the following formula (IV):
in which R3 represents an alkyl- or alkenyl group having from 10 to 18 carbon atoms, and R4 and R5 independently represent an alkyl groups having 1 or 2 carbon atoms,
Higher fatty acid alkanol amides or ethylene oxide adducts thereof may be the compounds represented by the following formula (V):
in which R6 represents an alkyl- or alkenyl group having from 10 to 18 carbon atoms, b is a value of from 1 to 3 and c is a value of from 0 to 3.
The following compounds (1) through (5) are given as examples of nitrogen-free polyoxyalkylene addition type non-ionic surface active agents having from 50 to 300 oxyalkylene groups per molecule, i.e. the component (C):
(1) polyoxyalkylene alkyl- or alkenyl ethers and polyoxyalkylene fatty acid esters represented by the following formula (VI): R7-O-(AO)dR8 (VI) in which R7 represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms, Re represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, A represents an ethylene or propylene group, and d is a value of from 50 to 300.
(2) polyoxyalkylene glycerol alkyl- or alkenyl ethers and polyoxyalkylene glycerol fatty acid esters represented by the following formula (VII):
in which R9, R10 and R,1, each independently represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, provided that at least one of Re, Rlo and R" is an alkyl- alkenyl- or acyl group, A represents an ethylene or propylene group, and e, f and g independently represent values of from 0 to 100, provided that the sum of e plus f plus d is from 50 to 300.
(3) polyoxyalkylene sorbitan alkyl- or alkenyl ethers, polyoxyalkylene sorbitol fatty acid esters represented by the following formula (Vlil):
in which R12 through R,7 each independently represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, provided that at least one of R,2 through R,7 is an alkyl-, alkenyl- or acyl group, A represents an ethylene or propylene group, and h, i, j, k, I and m independently represent values of from 0 to 100, provided that the sum of h through m is from 50 to 300.
(4) polyoxyalkylene sorbitan alkyl- or alkenyl ethers and polyoxyalkylene sorbitan fatty acid esters represented by the following formula (IX):
in which Ri8 through R21 each independently represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, provided that at least one of Ris through R21 is an alkyl-, alkenyl- or acyl group, A represents an ethylene or propylene group, and n, o, p and q independently represent values of from 0 to 100, provided that the sum of n, o, p, and q is from 50 to 300.
(5) polyoxyalkylene castor oils and polyoxyalkylene hydrogenated castor oils or their derivatives with an average value of the added oxyalkylenes of from 50 to 300 moles.
The polyoxyalkylene type non-ionic surface active agent as illustrated above are characterized in that they have a long chained oxyalkylene groups. A suitable number of moles of the alkylene oxide to be added, however, is in a range of from 50 to 300, preferably 70 to 200. The compound will exhibit a decreased detergency at a low concentration and tend to impair the foaming of the detergent when the number of moles of the added alkylene oxide is less than 50. On the other hand, when the number of moles of alkylene oxide is more than 300 the compound becomes unacceptably viscous.
The liquid detergent composition according to this invention is formulated with 10 to 40% by weight of the component (A), 1 to 10% by weight of the component (B) and 0.5 to 10% by weight of the component (C).
Beside these essential components, the liquid detergent composition of this invention may be added with, as an optional ingredient, a conventional low temperature stabiiizer. Such a low temperature stabilizer may include lower alcohols such as ethanol and isopropanol; glycols such as ethylene glycol, polyethylene glycol, propylene glycol and polypropylene glycol; lower alkylbenznesulfonic acids containing an alkyl group or groups of from 1 to 6 carbon atoms such as benzenesulfonic acid, p-toluenesulfonic acid and xylenesulfonic acid; aromatic carboxylic acids such as benzoic acid and salicylic acid; and urea.
Other compounds known in the art as ingredients of a detergent may be formulated to the composition of this invention. Such compounds may include organic or inorganic builders for improving the detergency of a detergent composition, inclusive of citric acid, malic acid, gulconic acid and salts of these compounds, skin roughening preventives, enzymes, protein derivatives, opacity promoting agents, coloring agents, preservatives, perfumes and the like.
In practice, it is desirable that the liquid detergent composition of this invention have a pH of from 5 to 9, more preferably from 6 to 8.
The liquid composition of this invention exhibits an excellent detergency and foaming ability at a low concentration of less than 1%. Thus, the composition not only possesses a strong detergency and foaming ability which any detergent is supposed to inherently possess, but also prevents washing hands from getting roughened and provides an economy because of usability at such a low concentration. Thus the composition has a wide variety of use, including particularly a detergent for washing dishes and other tablewares.
Other features of the invention will become apparent in the course of the following description of the exemplary embodiments which are given for illustration of the invention and are not intended to be limiting thereof.
EXAMPLES
In the examples below properties of tested detergents were determined according to the following test methods.
Detergency Evaluation Test
(1) Preparation of dirt bath: A dirt bath was prepared by dissolving 20 g of a mixed oil and fat consisting of 1 part of beef tallow and 1 part of soybean oil, both meeting the specification of the Japanese pharmacopoeia, and 0.1 g of oil red in 60 ml of chloroform.
(2) Preparation of stained glass plate specimens: Clean glass plates, 6 pieces for one set, were used for the test. Each glass plate was weighed precisely down to three place of decimal, dipped in the dirt bath to the depth of 55 mm at 25+ 10C for 1-2 minutes thus having stains attached thereto, and then taken out of the bath. Surplus of stains or dirt attached to the lower part of the glass plate were adsorbed by means of clean cloth like gauze or filter paper to obtain a uniform dirt on the glass plate, which was then air-dried at 25+ 10C for more than 1 hour and longer than 2 hours before it was submitted to the test. At this instance the quantity of the dirt or stains on each set of 6 glass plates adjusted to 0.140+0.010 g.
(3) Water
Water with a hardness of 3 DH (CaO/MgO molar ratio: 3/1) was employed. 59.0 mg of calcium chloride (dihydrate) and 27.2 mg of magnesium chloride (hexahydrate) each precisely weighed were dissolved in water to make the total volume to 1,000 ml.
(4) Test Procedure
Cleansing: One set of the stained glass plates prepared in (2) above were put into 700 ml of a 0.15% detergent solution, and washed by means of a Linnets modified detergency tester (250t 10 rpm) at 30+1 C for a prescribed period of time.
Rinse: The glass plates having been cleansed as above were put into 700 ml of water prescribed in (3) above and rinsed using the Linnets modified detergency tester at 30+ 1"C for 1 minutes.
Drying: The glass plates having been rinsed as above were air-dried for overnight and submitted to the evaluation of the detergency.
(5) Detergency evaluation
The glass plate specimens were weighed to determine the proportion of removed stains or dirt (%) to make it a standard of detergency evaluation.
Foaming Ability Evaluation Test
Foaming ability was measured on a 0.5% detergent solution added with 0.1% of commercially available butter, as a dirt component. Forty (40) cc of the detergent solution containing butter was put in a glass cylinder with a diameter of 5 cm, agitated rotationally for 10 minutes, and then the height of the foam attained was measured immediately after terminating the agitation.
In the following description and in the Tables following notes are applicable:
Notes:
(i) "POE" denotes polyoxyethylene.
(ii) Values in parentheses immediately following "POE" designate number of moles of added oxyethylene.
(iii) Formulated quantities of each component in Tables are expressed by weight %.
(iv) In Table 3, "Tr" designates that the composition is transparent, "Tu/W" designates it is turbid and white, and "Tr/V" means that it is transparent and highly viscous (3,000 cps at 20"C) Example 1
Detergency and foaming ability were tested on various detergent compositions according to the test procedures described above. The results obtained are shown in Table 1.
Example 2.
Detergency and foaming ability were evaluated on the detergent compositions described below and Table 2. The results are shown in Table 2.
[Formulation]
Raw Materials Proportions (wt%) Sodium POE(3)* laurylsulfate 20
Lauryldimethylamine oxide 5
Long chained POE* type non-ionic 0-8 surface active agent (see Table 2)
Ethanol 5
Water Balance
Example 3.
Detergency and foaming ability were evaluated on the detergent compositions appearing in
Table 3. The appearances of the detergent compositions at normal temperature were observed.
The results are shown in Table 3.
Table 1
Comparative Compositions Inventive Compositions
Law Materials 1 2 3 4 5 6 7 8 9 10 11 12
Sodium POE(3) 15 15 laurylether sulfate
Sodium laurylbenzene 15 15 sulfonate
Sodium α-olefin 15 15 sulfonate (Average carbon number = 14)
Sodium alkanesulfonate 15 15 (Aberage carbon number = 18)
Sodium α;-sulfoethyl 15 15 laurate
Sodium POE(3) 15 15 laurylether acetate
Coconut oil fatty acid 5 3 3 5 3 3 diethanol amide
Lauryldimethylamine 3 2 3 2 3 2 3 2 oxide
Lauryl betain 7 7
POE(100) cetylether 2 2 2 2 2 2
Ethanol 5 5 5 5 5 5 5 5 5 5 5 5
Water ("B" denotes B B B B B B B B B B B B "Balance")
Detergency Test (%) 56 50 42 53 58 45 81 79 80 78 85 82
Foaming Abilty Test (mm) 80 90 75 80 85 80 80 90 75 80 85 80 Table 2
Comparative
Long-chained POE type Compodition Inventive Compositions non-ionic surface active agent 13 14 15 16 17 18 19 20 21
POE(70) - 1 - - - - - -
Laurylether
POE(100) - - 1 - - - - -
Oleylether
POE(140) - - - 0.5 - - - -
Monostearate
POE(140) - - - - 1 - - -
Distearate
POE(200) - - - - - 2 - -
Sorbitan trioleate
POE(100) - - - - - - 5 -
Glycerol monostearate
POE(200) - - - - - - - 8
Sorbitol tetraoleate
POE(280) - - - - - - - - 5
Hydrogenated castor oil
Detergency Test (%) 58 80 82 88 91 86 85 85 79
Foaming Ability (mm) 95 95 97 95 95 96 95 93 95
Test Table 3
Comparative Compositions Inventive Compositions
Raw Materials 22 23 24 25 26 27 28
Sodium laurylbenzene 20 20 20 20 20 20 20 sulfonate
Coconut oil fatty 5 5 5 5 5 5 5 acid diethanol amide
POE(5) - 2 - - - -
Stearyl ether
POE(30) - - 2 - - -
Stearyl ether
POE(45) - - - 2 - -
Stearyl ether
POE(60) - - - - 2 -
Stearyl ether
POE(100) - - - - - 2
Stearyl ether
POE(250) - - - - - - 2
Stearyl ether
Ethanol 5 5 5 5 5 5 5
Water B B B B B B B
Detergency Test (%) 46 43 50 53 78 82 88
Foaming Ability (mm) 95 38 42 68 90 95 95
Test
Appearance Tr Tu/W Tr Tr/V Tr/V Tr/V Tr/V Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.
Claims (16)
1. A liquid detergent composition comprising:
(A) from 10 to 40% by weight of a snythesized anionic surface active agent,
(B) from 1 to 10% by weight of a nitrogen-containing amphoteric or non-ionic surface active agent, and
(C) from 0.5 to 10% by weight of a nitrogen-free polyoxyalkylene addition type non-ionic surface active agent having from 50 to 300 oxyalkylene groups per molecule.
2. A liquid detergent composition according to claim 1, wherein said component (A) is selected from polyoxyethylene alkyl- or alkenyl ether sulfates, alkylbenzenesulfonates, polyoxyethylene alkyl- or alkenyl ether acetates, a-olefin sulfonates, alkane sulphonates, salts of asulfofatty acid esters.
3. A liquid detergent composition according to claim 1, wherein said component (A) is selected from polyoxyethylene alkyl- or alkenyl ether sulfates, or alkylbenzenesulfonates.
4. A liquid detergent composition according to claim 1, wherein said component (B) is selected from mono long chained alkyl- or alkenyl tert-amine oxides, or higher fatty acid alkanol amides or ethylene oxide adducts thereof.
5. A liquid detergent composition according to claim 1, wherein said component (C) comprises at least one compound selected from polyoxyalkylene alkyl- or alkenyl ethers, polyoxyalkylene fatty acid esters, polyoxyalkylene glycerol alkyl- or alkenyl ethers, polyoxyalkylene glycerol fatty acid esters, polyoxyalkylene sorbitan alkyl- or alkenyl ethers, polyoxyalkylene sorbitan fatty acid esters, polyoxyalkylene sorbitol alkyl- or alkenyl ethers, polyoxyalkylene sorbitol fatty acid esters, polyoxyalkylene castor oils, or polyoxyalkylene hydrogenated castor oils.
6. A liquid detergent composition as claimed in claim 3, wherein said component (A) is a polyoxyethylene alkyl- or alkenyl ether sulfate represented by the following formula (I): R1O(CH2CH20)aSO3M (I) in which R, represents an alkyl- or alkenyl group having from 10 to 24 carbon atoms, a is a value of from 1 to 5, M represents an alkali metal, ammonium or an alkanolamine group.
7. A liquid detergent composition as claimed in claim 3 wherein component (A) is an alkylbenzenesulfonate represented by the following formula (ill):
in which R2 represents an alkyl group having 8 to 20 carbon atoms and M represents an alkali metal, ammonium or alkanolamine group.
8. A liquid detergent composition as claimed in claim 4 wherein component (B) is a mono long chained alkyl- or alkenyl tert-amine oxide as represented by the following formula (IV):
in which R3 represents an alkyl- or alkenyl group having from 10 to 18 carbon atoms, and R4
and R5 independently represent alkyl groups having 1 or 2 carbon atoms.
9. A liquid detergent composition as claimed in claim 4 wherein component (B) is a higher fatty acid alkenyl amine or ethylene oxide adduct thereof represented by the following formula (V):
in which R6 represents an alkyl- or alkenyl group having from 10 to 18 carbon atoms, b is a value of from 1 to 3 and c is a value of from 0 to 3.
10. A liquid detergent composition as claimed in claim 5 wherein component (C) comprises a polyoxyalkylene alkyl- or alkenyl ether, or polyoxyalkylene fatty acid ester represented by the following formula (VI): R7O-(AO)dR8 (Vl) in which R7 represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms, R8 represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, A represents an ethylene or propylene group, and d is a value of from 50 to 300.
11. A liquid detergent composition as claimed in claim 5, wherein component (C) comprises polyoxyalkylene glycerol alkyl- or alkenyl ethers and polyoxyalkylene glycerol fatty acid esters represented by the following formula (VII): CH2O(AO)eR5 CHO(AO)Ro (VII) CH2O(AO)gR1i in which R9, Rlo and R11, each idependently represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, provided that at least one of R9, R10 and R" is an alkyl-, alkenyl- or acyl group, A represents an ethylene or propylene group, and e, f and g independently represent values of from 0 to 100, provided that the sum of e plus f plus d is from 50 to 300.
12. A liquid detergent composition as claimed in claim 5 wherein component (C) comprises a polyoxyalkylene sorbitan alkyl- or alkenyl ethers, polyoxyalkylene sorbitol fatty acid esters represented by the following formula (VIII):
in which R12 through R,7 each independently represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, provided that at least one of R12 through R,7 is an alkyl-, alkenyl- or acyl group, A represents an ethylene or propylene group, and h, i, j, k, I and m independently represent values of from 0 to 100, provided that the sum of h through m is from 50 to 300.
13. A liquid detergent composition as claimed in claim 5 wherein the component (C) comprises a polyoxyalkylene sorbitan alkyl- or alkenyl ethers and polyoxyalkylene sorbitan fatty acid esters represented by the following formula (IX):
in which R,8 through R2, each independently represents an alkyl-, alkenyl- or acyl group having from 10 to 24 carbon atoms or a hydrogen atom, provided that at least one of R,8 through R2, is an alkyl-, alkenyl- or acyl group, A represents an ethylene or propylene group, and n, o, p and q independently represent values of from 0 to 100, provided that the sum of n, o, p, and q is from 50 to 300.
14. A liquid detergent composition as claimed in any one of the preceding claims wherein the nitrogen-free polyoxylalkylene addition type non-ionic surface active agent comprises from 70 to 200 oxyalkylene groups per molecule.
15. A liquid detergent composition as claimed in any one of the preceding claims having a
PH of from 5 to 9 and preferably from 6 to 8.
16. A liquid detergent composition substantially as hereinbefore described.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61232589A JPS6386798A (en) | 1986-09-30 | 1986-09-30 | Liquid detergent composition |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8721893D0 GB8721893D0 (en) | 1987-10-21 |
GB2197338A true GB2197338A (en) | 1988-05-18 |
GB2197338B GB2197338B (en) | 1990-09-26 |
Family
ID=16941729
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8721893A Expired - Fee Related GB2197338B (en) | 1986-09-30 | 1987-09-17 | Liquid detergent composition |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPS6386798A (en) |
GB (1) | GB2197338B (en) |
HK (1) | HK32691A (en) |
MY (1) | MY101450A (en) |
PH (1) | PH24938A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5230823A (en) * | 1989-05-22 | 1993-07-27 | The Procter & Gamble Company | Light-duty liquid or gel dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant |
EP0586323A1 (en) * | 1992-07-20 | 1994-03-09 | Kao Corporation, S.A. | Detergent composition and method for its preparation |
US5376310A (en) * | 1990-11-16 | 1994-12-27 | The Procter & Gamble Co. | Alkaline light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant, magnesium ions, chelator and buffer |
US5378409A (en) * | 1990-11-16 | 1995-01-03 | The Procter & Gamble Co. | Light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant and ions |
US5403509A (en) * | 1992-07-20 | 1995-04-04 | Kao Corporation, S.A. | Detergent composition comprising a mono-, di- and tri-ester mixture and method of manufacturing same |
EP0723004A1 (en) * | 1994-08-10 | 1996-07-24 | Kao Corporation | Detergent composition |
WO1996022347A1 (en) * | 1995-01-17 | 1996-07-25 | Colgate-Palmolive Company | Light duty liquid cleaning compositions |
US5686403A (en) * | 1993-09-24 | 1997-11-11 | Kao Corporation | Cleanser composition containing phosphate ester and ether acetate surfactants |
WO1999030606A1 (en) * | 1997-12-02 | 1999-06-24 | Tord Georg Eriksson | Rinse method |
WO2000066684A1 (en) * | 1999-04-30 | 2000-11-09 | Colgate-Palmolive Company | Liquid cleaning compositions containing a methyl ethoxylated ester |
EP1832931A1 (en) * | 2004-12-09 | 2007-09-12 | Tokyo Ohka Kogyo Co., Ltd. | Cleaning liquid for lithography and method for resist pattern formation |
EP2792241A4 (en) * | 2011-12-12 | 2015-09-23 | Oxiteno Sa Ind E Comercio | Thickening composition for use in agrochemical formulations, use of a thickening composition and agrochemical formulations containing a thickening composition |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03106999A (en) * | 1989-09-20 | 1991-05-07 | Kanebo Ltd | Lowly irritant detergent composition |
WO2011046170A1 (en) * | 2009-10-15 | 2011-04-21 | ライオン株式会社 | Liquid detergent composition |
KR101980398B1 (en) * | 2011-09-20 | 2019-05-21 | 헨켈 아이피 앤드 홀딩 게엠베하 | Cleaning formulations with improved surfactant solubility and methods of production and use thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS609693B2 (en) * | 1977-09-12 | 1985-03-12 | ライオン株式会社 | Shampoo - Composition |
US5167872A (en) * | 1985-10-31 | 1992-12-01 | The Procter & Gamble Company | Comprising anionic surfactant polymeric nonionic surfactant and betaine surfactant |
AU589225B2 (en) * | 1985-10-31 | 1989-10-05 | Procter & Gamble Company, The | Liquid detergent composition |
US4803010A (en) * | 1986-09-18 | 1989-02-07 | Kao Corporation | Water-soluble viscosity increasing agent and detergent composition containing the same |
-
1986
- 1986-09-30 JP JP61232589A patent/JPS6386798A/en active Granted
-
1987
- 1987-09-16 PH PH35824A patent/PH24938A/en unknown
- 1987-09-17 GB GB8721893A patent/GB2197338B/en not_active Expired - Fee Related
- 1987-09-28 MY MYPI87002060A patent/MY101450A/en unknown
-
1991
- 1991-05-02 HK HK326/91A patent/HK32691A/en not_active IP Right Cessation
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5230823A (en) * | 1989-05-22 | 1993-07-27 | The Procter & Gamble Company | Light-duty liquid or gel dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant |
US5376310A (en) * | 1990-11-16 | 1994-12-27 | The Procter & Gamble Co. | Alkaline light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant, magnesium ions, chelator and buffer |
US5378409A (en) * | 1990-11-16 | 1995-01-03 | The Procter & Gamble Co. | Light duty dishwashing detergent composition containing an alkyl ethoxy carboxylate surfactant and ions |
EP0586323A1 (en) * | 1992-07-20 | 1994-03-09 | Kao Corporation, S.A. | Detergent composition and method for its preparation |
US5403509A (en) * | 1992-07-20 | 1995-04-04 | Kao Corporation, S.A. | Detergent composition comprising a mono-, di- and tri-ester mixture and method of manufacturing same |
US5686403A (en) * | 1993-09-24 | 1997-11-11 | Kao Corporation | Cleanser composition containing phosphate ester and ether acetate surfactants |
EP0723004A4 (en) * | 1994-08-10 | 1999-04-28 | Kao Corp | Detergent composition |
EP0723004A1 (en) * | 1994-08-10 | 1996-07-24 | Kao Corporation | Detergent composition |
WO1996022347A1 (en) * | 1995-01-17 | 1996-07-25 | Colgate-Palmolive Company | Light duty liquid cleaning compositions |
WO1999030606A1 (en) * | 1997-12-02 | 1999-06-24 | Tord Georg Eriksson | Rinse method |
WO2000066684A1 (en) * | 1999-04-30 | 2000-11-09 | Colgate-Palmolive Company | Liquid cleaning compositions containing a methyl ethoxylated ester |
EP1832931A1 (en) * | 2004-12-09 | 2007-09-12 | Tokyo Ohka Kogyo Co., Ltd. | Cleaning liquid for lithography and method for resist pattern formation |
EP1832931A4 (en) * | 2004-12-09 | 2010-05-26 | Tokyo Ohka Kogyo Co Ltd | Cleaning liquid for lithography and method for resist pattern formation |
US7795197B2 (en) | 2004-12-09 | 2010-09-14 | Tokyo Ohka Kogyo Co., Ltd. | Cleaning liquid for lithography and method for resist pattern formation |
CN101076759B (en) * | 2004-12-09 | 2010-12-01 | 东京应化工业株式会社 | Cleaning liquid for lithography and method for resist pattern formation |
EP2792241A4 (en) * | 2011-12-12 | 2015-09-23 | Oxiteno Sa Ind E Comercio | Thickening composition for use in agrochemical formulations, use of a thickening composition and agrochemical formulations containing a thickening composition |
Also Published As
Publication number | Publication date |
---|---|
PH24938A (en) | 1990-12-26 |
JPS6386798A (en) | 1988-04-18 |
GB8721893D0 (en) | 1987-10-21 |
HK32691A (en) | 1991-05-10 |
GB2197338B (en) | 1990-09-26 |
MY101450A (en) | 1991-11-18 |
JPH0359119B2 (en) | 1991-09-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19980917 |