GB2273300A - Hard surface cleaning compositions - Google Patents
Hard surface cleaning compositions Download PDFInfo
- Publication number
- GB2273300A GB2273300A GB9310677A GB9310677A GB2273300A GB 2273300 A GB2273300 A GB 2273300A GB 9310677 A GB9310677 A GB 9310677A GB 9310677 A GB9310677 A GB 9310677A GB 2273300 A GB2273300 A GB 2273300A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon atoms
- detergent composition
- individually
- component
- mean
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- 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
- C11D1/8305—Mixtures of non-ionic with anionic compounds containing a combination of non-ionic compounds differently alcoxylised or with different alkylated chains
-
- 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
- C11D1/24—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds containing ester or ether groups directly attached to the nucleus
-
- 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
- C11D1/65—Mixtures of anionic with cationic compounds
- C11D1/652—Mixtures of anionic compounds with carboxylic amides or alkylol amides
-
- 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
-
- 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
- C11D1/86—Mixtures of anionic, cationic, and non-ionic compounds
-
- 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
-
- 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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2068—Ethers
-
- 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
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/28—Heterocyclic compounds containing nitrogen in the ring
-
- 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
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- 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
-
- 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
- C11D1/662—Carbohydrates or derivatives
-
- 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
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D1/72—Ethers of polyoxyalkylene glycols
- C11D1/721—End blocked ethers
-
- 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
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
-
- 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
-
- 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
- C11D1/90—Betaines
-
- 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
- C11D1/92—Sulfobetaines ; Sulfitobetaines
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Abstract
A detergent composition for cleaning hard surfaces comprises: a diphenyl ether disulfonate anionic surfactant, a water-soluble organic solvent, an amino compound, and water. The composition is especially easy to wipe off the cleaned surface.
Description
TITLE OF THE INVENTION:
DETERGENT COMPOSITION FOR HARD SURFACES
BACKGROUND OF THE INVENTION i) Field of the Invention:
This invention relates to a detergent composition for hard surfaces, and more specifically to a detergent composition for hard surfaces, which is excellent in easiness of wiping, scarcely remains on the surface cleaned after its wiping to give a good result, and possesses excellent detergency to dirt or smears, in particular, deteriorated oil and grease smears.
ii) Description of the Background Art:
As detergent compositions for hard surfaces, the following compositions have hitherto been used properly according to the kind and degree of dirt.
Namely, surfactant-solvent type detergents and surfactant-solvent-alkaline agent type detergents have been principally used respectively for dirt from the hands and undeteriorated oil and grease smears, which are relatively light in degree of dirt, and for oil and fat smears appeared in or near a kitchen and deteriorated by an action of heat, sunlight, oxygen in air and/or the like, and the like.
However, when these detergents are used, the surfactant and alkaline agent remain on the surfaces cleaned after wiping off the detergents, so that wipe streaks are left even after the cleaning, leading to an insufficient result.
Therefore, these detergents require double wiping or sufficient rinsing with water, and are hence complicated.
As an attempt to solve such a problem, Japanese Patent
Application Laid-Open No. 29498/1990 discloses a liquid housecleaning detergent composition which comprises, as essential components, an anionic surfactant, a terpene hydrocarbon solvent and a water-soluble salt of a divalent metal, is excellent in cleansability and safe for the human body, scarcely affects substrates, and requires no rinsing.
This detergent composition has shown a considerable improvement from the viewpoint of finish upon cleaning a glass surface or the like, but has required a further improvement from the viewpoint of practical use. Japanese
Patent Application Laid-Open No. 501570/1987 (through PCT route) discloses a detergent composition composed of a glycoside surfactant, a solvent, a water-soluble detergent and a builder. However, this composition has also required sufficient rinsing because a portion of the composition has been observed remaining after wiping it.
Further, Japanese Patent Application Laid-Open No.
85400/1992 has proposed a liquid detergent composition which comprises a specific anionic surfactant and a specific amphoteric surfactant, has high detergency and leaves little wipe streaks. This composition has however overfoamed upon its wiping due to its high foaming power, and has hence been poor in easiness of wiping (easiness of wiping operation).
On the other hand, alkyl diphenyl ether type surfactants having two sulfonic groups in their molecules have heretofore been used widely, for example, as emulsifiers upon preparation of polymers, chemical agents for fiber-dyeing processes, dispersing agents for agricultural chemicals and dispersants for crude oil sludge.
However, it has not been known to use them in surfactantsolvent-amine compound type detergents for hard surfaces.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a detergent composition for hard surfaces, which is excellent in easiness of wiping, to say nothing of detergency, and leaves little wipe streaks to give a good result,
In view of the foregoing circumstances, the present inventors have carried out an extensive investigation. As a result, it has been found that when a diphenyl ether disulfonate type anionic surfactant, a water-soluble solvent and an amine compound are blended, a detergent composition which has excellent detergency to dirt, in particular, deteriorated oil and fat smears, is good in easiness of wiping, and scarcely leaves wipe streaks to give a good result, leading to completion of the present invention.
In an aspect of the present invention, there is thus provided a detergent composition for hard surfaces, which comprises the following components (A), (B) and (C):
(A) a diphenyl ether disulfonate type anionic surfactant,
(B) a water-soluble solvent, and
(C) an amine compound.
In another aspect of this invention, there is also provided a detergent composition for hard surfaces, which comprises the following components (A), (B) and (C):
(A) 0.01-20 wt.% of a diphenyl ether disulfonate type anionic surfactant,
(B) 0.1-50 wt.% of a water-soluble solvent, and
(C) 0.01-30 wt.% of an amine compound.
The detergent compositions for hard surfaces according to the present invention have high detergency, in particular, to deteriorated oil and grease smears, are excellent in easiness of wiping, scarcely remains on the surfaces cleaned after their wiping and also show good finishing behavior.
The above and other objects, features and advantages of the present invention will be readily appreciated from the preferred embodiments of the present invention, which will be described subsequently in detail.
DETAILED DESCRIPTION OF THE INVENTION
AND PREFERRED EMBODIMENTS
No particular limitation is imposed on the component (A) useful in the practice of this invention so long as it is a diphenyl ether disulfonate. However, it may preferably comprise one or more anionic surfactants selected from compounds represented by the following general formulae (1) and (2):
wherein R1 and R2 mean individually a linear or branched alkyl or alkenyl group having 5-15 carbon atoms, and M and
M' denote individually an alkali metal atom, an ammonium group or an alkanol-substituted ammonium group.
R1 and R2 in the above general formulae may be individually a linear or branched alkyl or alkenyl group having 5-15 carbon atoms. However, alkyl groups having 8-14 carbon atoms, in particular, alkyl groups having 12-14 carbon atoms are preferred in that the resulting detergent composition has good detergency and leaves little wipe streaks, M and M' may be indivisually an alkali metal atom such as a sodium or potassium atom, an ammonium group, or an alkanol-substituted ammonium group such as monoethanolammonium or diethanolammonium. Of these, alkali metal atoms are particularly preferred. As the component (A), two compounds respectively selected from the surfactants represented by the formulae (1) and (2) may preferably be used in a proportion of from 100/0 to 25/75, in particular, from 95/5 to 70/30 by weight.Incidentally, the compounds represented by the above general formulae (1) and (2) can be separately obtained in accordance with the conventionallyknown process in which diphenyl ether is alkylated by the
Friedel-Crafts reaction, the resulting product is sulfonated with sulfur trioxide or the like in a dichloromethane solvent, and the resultant sulfonic compound is then neutralized. The alkylation reaction of diphenyl ether may take place selectively at a para position, but alkylates different in number of alkyl groups substituted or orientation site may be obtained by differences of reaction conditions such as the amount of an alkylating agent to be used. However, no serious problem is posed so far as the compounds represented by the formulae (1) and (2) are contained as principal components.
No particular limitation is imposed on the component (B) useful in the practice of this invention so long as it is a water-soluble solvent. However, it may preferably comprise one or more water-soluble solvents selected from compounds represented by the following general formulae (3) through (5):: R3O(C2H4O)m(C3H6O)nR4 (3)
R70C(CH3)2(CH2CH20H (5) wherein R3 and R4 mean individually a hydrogen atom or an alkyl group having 1-8 carbon atoms, with the proviso that both groups R3 and R4 do not mean hydrogen atoms at the same time, m and n stand individually for an integer of 0-3, with the proviso that both m and n do not stand for integers of O at the same time, R5 and R6 denote individually an alkyl group having 1-3 carbon atoms, and R7 means an alkyl group having 1-3 carbon atoms, dihydric alcohols having 4-12 carbon atoms and monohydric alcohols having 1-5 carbon atoms.
In the water-soluble solvent represented by the general formula (3), R3 and R4 may be individually a hydrogen atom or an alkyl group having 1-8 carbon atoms, with an alkyl group having 1-4 carbon atoms being particularly preferred. In the formula (3), m and n, which mean respectively the average numbers of moles of ethylene oxide (E.O.) and propylene oxide (P.O.) added, may preferably be 0-3. No particular limitation is imposed on the sequence of addition of these oxides. The addition may be conducted at random.As specific examples of the compound of the formula (3), may be mentioned ethylene glycol monobutyl ether, dipropylene glycol dimethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, propylene glycol monomethyl ether, propylene glycol monobutyl ether, propylene glycol monoethyl ether, propylene glycol dimethyl ether, polyoxyethylene (p = 1) polyoxypropylene (p = 1) glycol dimethyl ether (p denotes an average number of moles added), and the like.
Among these compounds of the formula (3), compounds represented by the following general formula (3') are particularly preferred from the viewpoint of detergency and easiness of wiping of the resulting detergent composition.
R3'0(C2H40)mr(C3H60),1R4' (3') wherein R31 and R41 mean individually a hydrogen atom or an alkyl group having 1-4 carbon atoms, with the proviso that both groups R3 and R4 do not mean hydrogen atoms at the same time, and m' and n' stand individually for an integer of 0-3, with the proviso that both m' and n' do not mean 0 at the same time, m' does not denote 1 and n' is not 0.
As specific examples thereof, may be mentioned propylene glycol monomethyl ether, diethylene glycol monobutyl ether and the like.
As preferable examples of the compound represented by the general formula (4), may be mentioned l,3-dimethyl-2- imidazolidinone and 1,3-diethyl-2-imidazolidinone. On the other hand, 3-methoxy-3-methylbutanol, 3-ethoxy-3-methylbutanol and the like are preferred as the compound represented by the general formula (5).
As examples of the dihydric alcohol having 4-12 carbon atoms, may be mentioned isoprene glycol, 2,2,4-trimethyl1,3-pentanediol and the like. As examples of the monohydric alcohol having 1-5 carbon atoms, may be mentioned methanol, ethanol, isopropanol and the like. When these lower alcohols are blended, the stability of the system at low temperatures can be more improved.
No particular limitation is imposed on the component (C) useful in the practice of this invention so long as it is an amine compound. However, it may preferably comprise one or more amine compounds selected from compounds represented by the following general formulae (6) through (9):
wherein R8, Rill, R13, R15, R17, R19 and R20 mean individually a hydrogen atom or an alkyl group having 1-4 carbon atoms, and R9, R1O, R12, R14 R16 and R18 denote individually a hydrogen atom, an alkyl group having 1-4 carbon atoms or a hydroxyalkyl group having 2-3 carbon atoms.
As exemplary compounds represented by the general formula (6), may be mentioned ammonia, monoethanolamine, diethanolamine, N-methylpropanolamine and the like.
As exemplary compounds represented by the general formula (7), may be mentioned N-(B-aminoethyl)ethanolamine and the like.
As exemplary compounds represented by the general formula (8), may be mentioned diethylenetriamine and the like.
As exemplary compounds represented by the general formula (9), may be mentioned morpholine, N-ethylmorpholine and the like.
Among these, monoethanolamine and morpholine are particularly preferred.
The detergent composition for hard surfaces according to a preferred embodiment of the present invention is -obtained by blending the above-described components (A), (B) and (C), and satisfies all of detergency, in particular, to deteriorated oil and grease smears, easiness of wiping, and finishing behavior. However, all such effects can not be exhibited if any one of these components is omitted.
In the detergent composition for hard surfaces according to another preferred embodiment of the present invention, the effects of the present invention can be more enhanced by blending the components (A), (B) and (C) in specific proportions. The component (A) may preferably be blended in a proportion of 0.01-20 wt.% (hereinafter indicated merely by "%"), more preferably 0.01-10%, most preferably 0.1-3% of the whole amount of the detergent composition. The component (B) may be preferably be blended in a proportion of 0.1-50%, more preferably 1-3u%, most preferably 1-20% of the whole amount of the detergent composition. The component (C) may be preferably be blended in a proportion of 0.01-30%, more preferably 0.01-20%, most preferably 0.05-10% of the whole amount of the detergent composition.Any amounts of the component (A) less than 0.01% result in a detergent composition insufficient in detergency. On the other hand, if the component (A) is blended in any proportion exceeding 20%, the effects of enhancing the easiness of wiping and finishing behavior according to the present invention are not expected to more heighten correspondingly. Any amounts of the component (B) less than 0.1t result in a detergent composition not wholly satisfied in detergency, while any proportions exceeding 50% result in a detergent composition impaired in finishing behavior. It is not hence preferable to blend the component (B) in any proportions outside the above range. If the amount of the component (C) is less than 0.01%, its influence on the detergent effect becomes insufficient, and its blending will hence mean little.On the other hand, if the component (C) is blended in any proportion exceeding 30%, the effects of the present invention can not be more heightened correspondingly.
The detergent compositions for hard surfaces according to the present invention may optionally contain, as a component (D), at least one surfactant other than those described above within limits not impeding the effects of the present invention. No particular limitation is imposed on such a surfactant. However, it may preferably comprise one or more surfactants selected from the group consisting of nonionic, anionic and amphoteric surfactants. Specific surfactants useful as the component (D) are as follows.
As examples of the anionic surfactants, may be mentioned alkylbenzene sulfonates, alkylene oxide-added alkyl (or alkenyl) ether sulfates, alkyl- or alkenylsulfates, olefinsulfonates, alkanesulfonates, fatty acid salts, alkylene oxide-added alkyl (or alkenyl) ether carboxylates, a-sulfo-fatty acid salts and esters thereof, and the like.
As examples of counter ions to the anionic surfactants, may be mentioned alkali metal ions such as sodium and potassium ions, ammonium ion, and alkanol substituted ammonium ions such as monoethanolammonium, diethanolammonium and triethanolammonium.
As examples of the nonionic surfactants, may be mentioned polyoxyalkylene alkyl (or alkenyl) ethers, polyoxyalkylene alkylphenyl ethers, sucrose fatty acid esters, fatty acid glyceryl esters, amine oxides, higher fatty acid alkanolamides or their addition products with alkylene oxides, and alkylglycosides represented by the following general formula (10): R21(OR22)xGy (10) wherein R21 means a linear or branched alkyl, alkenyl or alkylphenyl group having 8-18 carbon atoms, R22 denotes an alkylene group having 2-4 carbon atoms, G represents a residue derived from a reducing sugar having 5-6 carbon atoms, x stands for a number of 0-5 in terms of the average value, and y means a number of 1-10 in terms of the average value.
In the general formula (10), x is a number of 0-5 in terms of the average value. Both water-solubility and crystallinity of the detergent compositions according to the present invention are controlled by this value. Namely, the compositions have an inclination that the water-solubility becomes higher and the crystallinity becomes lower as x increases. The value of x is preferably 0-2, with 0 being particularly preferred. On the other hand, when y is greater than 1 in terms of the average value, namely, a surfactant represented by the general formula (10) and containing a di- or higher polysaccharide chain as a hydrophilic group is contained, the bond form of the saccharide chain may be a 1-2, 1-3, 1-4 or 1-6 bond, or an alpha- or beta-pyranoside or furanoside bond. It is also possible to contain any mixture having a combined form of these bonds.The average value of y in the general formula (10) may be 1-10, preferably 1-3, more preferably 1-1.5, most preferably 1-1.4. Incidentally, the measurement of y in this invention is based on the proton NMR method.
Further, R21 in the general formula (10) may be a linear or branched alkyl, alkenyl or alkylphenyl group having 8-18 carbon atoms. However, alkyl groups having 1014 carbon atoms are preferred from the viewpoint of improvement in solubility, foamability and cleansability.
Furthermore, R22 may be an alkylene group having 2-4 carbon atoms. However, the number of carbon atoms is preferably 23 from the viewpoint of the solubility in water. Moreover, the structure of G is dependent upon the raw material to be used, which is a monosaccharide or di- or higher polysaccharide. As examples of the raw material for G, may be mentioned monosaccharides such as glucose, fructose, galactose, xylose, mannose, lyxose, arabinose and mixtures thereof; and disaccharides and higher polysaccharides such as maltose, xylobiose, isomaltose, cellobiose, gentiobiose, lactose, sucrose, nigerose, turanose, raffinose, gentianose, melezitose and mixtures thereof. Of these, preferred materials are glucose and fructose for the monosaccharide, and maltose and sucrose for the di- or higher polysaccharide because of their good availability and low cost.Of these, glucose is particularly preferred from the viewpoint of availability.
In addition, examples of the nonionic surfactants include nonionic surfactants containing at least one longchain, branched alkyl or alkenyl group and at least three hydroxyl groups in their molecules, such as an addition compound of pentaerythritol with 1 mole of isostearyl glycidyl ether, an addition compound of sorbitol with 1 mole of isostearyl glycidyl ether, an addition compound of mannitol with 1 mole of 2-octyldodecyl glycidyl ether, an addition compound of methylglucoside with 1 mole of isostearyl glycidyl ether, an addition compound of diglycerol with 1 mole of isostearyl glycidyl ether, and phytanetriol.
As examples of the amphoteric surfactants, may be mentioned sulfobetaines and carbobetaines containing a linear or branched alkyl or alkenyl group having 1-22 carbon atoms, and the like.
In the present invention, among the above-mentioned surfactants, the higher fatty acid alkanolamides or their addition products with alkylene oxides, amine oxides, alkylglycosides, sulfobetaines and carbobetaines are preferred from the viewpoint of improvements in detergency and easiness of wiping, with the alkylglycosides being particularly preferred.
If these surfactants of the component (D) are blended, the proportion thereof is 0.01-20%, preferably 0.05-10%, most preferably 0.05-5%. If the amount of the surfactants is less than 0.01%, the surface activity brought by the component (D) is not sufficiently exhibited, and its blending will hence mean little. On the other hand, if the component (D) is blended in any proportion exceeding 20%, its effects are not expected to more heighten correspondingly. There is hence no need to blend the component (D) in an amount exceeding 20%.
In order to more improve the storage stability at low temperatures, the detergent compositions of this invention may optionally contain, in addition to the above-described components, the routinely-used dispersants, chelating agents, perfume bases, dyes, pigments, antiseptics and the like within limits not impeding the effects of the present invention.
The detergent compositions for hard surfaces can be prepared by mixing the aboveodescribed components and water in a method known Per se in the art.
The present invention will hereinafter be described in more detail by the following examples. However, it should be borne in mind that this invention is not limited to and by these examples.
EXAMPLES
Example 1:
Evaluation of detergency, easiness of wiping and
remaining behavior after wiping:
Detergent compositions for hard surfaces of their corresponding compositions shown in Tables 1-4 were separately prepared. Each of these detergent compositions was evaluated in detergency, easiness of wiping and remaining behavior after wiping in accordance with the following respective evaluation methods. These results are shown in Tables 1-4.
Evaluation methods for detergency, easiness of wiping and remaining behavior after wiping: [netergency Dirt from the hand was forcedly caused to adhere to a 10 x 10 cm glass plate, deteriorated by heat at 200"C for 30 minutes and left over further for 1 month at room temperature, thereby providing model dirt.
Each of the liquid detergent compositions was sprayed by 1 cc on the model dirt by a commercially-available sprayer and then wiped off with a dry towel, followed by its organoleptic evaluation in accordance with the following standard:
A: Dirt was removed to a very good extent.
B: Dirt was removed to a good extent.
C: Dirt was not removed in some places.
D: Dirt was scarcely removed.
[Easiness of wiping
Each of the liquid detergent compositions was sprayed by 3 cc on a window pane of a dwelling in actual use by a commercially-available sprayer and then wiped off with a dry towel. It was then evaluated organoleptically by the degree of foaming upon the wiping and the bursting rapidity of foams in accordance with the following standard:
A: Hard to foam when wiped with the towel.
(Foams burst at once when wiped)
B: Slightly foamed when wiped with the towel.
(Foams were hard to burst at once when wiped)
C: Highly foamed when wiped with the towel.
(Foams did not burst while wiping) [Remaining behavior after wiping (finishing behavior)]
After the detergent composition was evaluated in the easiness of wiping, its remaining behavior after the wiping was ranked in accordance with the following standard:
A: Scarcely left wipe streaks.
B: Slightly left wipe streaks.
C: Left wipe streaks.
Table 1
Invention product (%) 4 2 3 4 516 Na dodecyldiphenyl ether 10-5 0.5 1.0 2.0 I disulfonate 0.5 0.5 1.0 2.0 1.0 0.5 Na tetradecyldiphenyl ether | 0.5 0.5 | 0.4 disulfonate I Na didodecyldiphenyl ether 0.3 0.1 disul fonate Alkyl (c=ll) diethanolamide 0.3 Dodecylamine oxide 1 1 0.3 Alkyl (c=13) maltoside N, N, N-Lauryldimethyl-N 2 hyroxy-3-sulfopropy1 ammonium betaine Laurylamidopropyl-N,- I dimehylacetate-betalne Na alkyl (c=12) sulfate Polyoxyethylene (p=10) alkyl (a=12) ether Propylene glycol onomethy1 |1o 10 ether Diethylene glycol dimethyl l 1 10 ether 1,3-Dimethyl-2-imidazolidinone 10 3-Methoxy-3-methylbutanol 10 2,2,4-Trimethyl-1,3-pentanediol 10 Isopropanol | 10 Monoethanolamine | 1 |0-5 0.5 3 N- (-Aminoethyl) ethanolamine I 1 3 Morphol ine Na carbonate Na metasilicate Na tertiary phosphate I Water Bal Bal Bal |Bal Bal Bal Bal L I Detergency B | B | A | A | B | A Easiness of wiping | A | A | A | A | A | A 4 Remaining behavior ,, A | A | A | A | A | A l Bal:Balance
Table 2
Invention product (t) 7 8 8 9 1 10 11 Na dodecyldiphenyl ether 0.5 0.5 1.0 0.5 1.5 disul 0.5 0.5 1,0 0.5 fonate Na tetradecyldiphenyl ether 0.5 0.5 0.5 disulfonate Na didodecyldiphenyl ether disul fonate Alkyl (c=ll) diethanolamide Dodecylamine oxide 0.3 0.3 Alkyl (c=13) maltoside 0.3 N,N,N-Lauryldimethyl-N-2- 0.3 hydroxy-3-sulfopropyl- 0.3 1 ammonium betaine Laurylamidopropyl-N,N- 0.3 dimethylacetate betaine Na alkyl (c=12) sulfate 0.3 Polyoxyethylene (p=10) 0.3 alkyl (c=12) ether Propylene glycol monomethyl 10 ether Diethylene glycol dimethyl 10 ether 1, 3-Dimethyl-2-imidazolidinone 10 3-Methoxy-3-methylbutanol 10 2,2,4-Trimethyl-1,3-pentanediol 10 Isopropanol Monoethanolamine 1 1 N-(B-Aminoethyl)ethanolamine Morpholine 0.5 1 3 Na carbonate Na metasilicate Na tertiary phosphate Water Bal Bal Bal Bal Bal 6 X Detergency B B | A A | A Easiness of wiping A A | A | A | A r Remaining behavior A A | A ! A | A Bal:Balance
Table 3
Comparative product (%) 1 ! 2 3 1 4 5 1 6 Na dodecyldiphenyl ether disulfonate 1.0 0.5 Na tetradecyldiphenyl ether 1.0 0.5 disul fonate Na didodecyldiphenyl ether disulfonate 1.0 Alkyl (c=ll) diethanolamide Dodecylamine oxide 2 0.3 Alkyl (c=13) maltoside N, N, N-Lauryldimethyl -N- 2 hydroxy-3 -sulfopropyl ammonium betaine Laurylamidopropyl-N,N dime hylace ate betaine Na alkyl (c=12) sulfate 1.0 Polyoxyethylene (p=10) 1.0 alkyl (c=12) ether Propylene glycol onomethy1 | |10 10 ether Diethylene glycol dimethyl l 10 ether 1,3-Dimethyl-2-imidazolidinone ! Z lO I 3-Methoxy-3-methylbutanol 10 2,2,4-Trimethyl-1,3-pentanediol 10 Isopropanol l I Monoethanolamine | 1 F 1 N-(8-Aminoethyl)ethanolamine 1 I I Morphol ine 1 Na carbonate j l l 1 Na metasilicate Na tertiary phosphate l I Water Bal Bal Bal |Bal Bal |Bal Bal Bal I I ≈ A Detergency | D | D B B B C Easiness of wiping | A | A C | C | B C z Remaining behavior ! A ! A B I C ss C C Bal:Balance
Table 4
Comparative proauct (%) 7 8 Na dodecyldiphenyl ether 1.0 disulfonate Na tetradecyldiphenyl ether 0 1.0 disul fonate Na didodecyldiphenyl ether disulfonate Alkyl (c=ll) diethanolamide I Dodecylamine oxide Alkyl (c=13) maltoside 0.3 N,N,N-Lauryldimethyl-N-2 hydroxy-3 -sul fopropyl - 0.3 ammonium betaine Laurylamidoropyl-N, dimethylaceate betalne Na alkyl (=12) sulfate 0.3 Polyoxvethylene (=10) 0.3 alkyl 7=12) eth.er Propylene glycol monomethyl ether Diethylene glycol dimethyl ether 1,3-Dimethyl-2-imidazolidinone 3-Methoxy-3-methylbutanol 2,2, 4-Trimethyl-l, 3-pentanediol Isopropanol 10 10 Monoethanolamine N- (p-Aminoethyl) ethanolamine Morpholine Na carbonate Na metasilicate 1 Na tertiary phosphate 1 Water Bal Bal ; ffi Detergency B B Easiness of wiping B C t 4 Remaining behavior C C Bal: Balance
Example 2:
Evaluation of detergency, easiness of wiping and
remaining behavior after wiping:
Detergent compositions for hard surfaces of their corresponding compositions shown in Table 5 were separately prepared.Each of these detergent compositions was evaluated in detergency, easiness of wiping and remaining behavior after wiping in accordance with the following respective evaluation methods. These results are shown in
Table 5.
Evaluation methods for detergency, easiness of wiping and remaining behavior after wiping: [Detergency]
After tempura oil was heated at 200-220 C for 18 hours, air was blown in the oil at 100"C to treat it for 8 hours, thereby deteriorating the oil. The thus-deteriorated oil was applied to the surface of a stainless steel plate.
The thus-coated stainless steel plate was left over for 2 months at room temperature. Each of the liquid detergent compositions was spread on the oil smear adhered on the surface of the stainless steel plate, left over for 3 minutes and then wiped off with a dry towel, followed by its organoleptic evaluation in accordance with the following standard:
A: Smear was removed to a very good extent.
B: Smear was removed to a good extent.
C: Smear was not removed in some places.
D: Smear was scarcely removed.
[Easiness of wiping]
Each of the liquid detergent compositions was spread by 3 cc on a kitchen range (made of a stainless steel) in actual use and then wiped off with a dry towel. It was then evaluated organoleptically by the degree of foaming upon the wiping and the bursting rapidity of foams in accordance with the following standard:
A: Hard to foam when wiped with the towel.
(Foams burst at once when wiped)
B: Slightly foamed when wiped with the towel.
(Foams were hard to burst at once when wiped)
C: Highly foamed when wiped with the towel.
(Foams did not burst while wiping) [Remaining behavior after wiping (finishing behavior)]
After the detergent composition was evaluated in the easiness of wiping, its remaining behavior after the wiping was ranked in accordance with the following standard:
A: Scarcely left wipe streaks.
B: Slightly left wipe streaks.
C: Left wipe streaks.
Table 5
Invention product Comparative product (%) I (%) 12 \ 13 1 14 1 15 ! 9 l 10 T 11 ! 12 Na dodecyldiphenyl 5 5 l 10 l 10 1 5 ether disulfonate Na tetradecyldiphenyl 1 3 1 1 3 ether disulfonate Alkyl (c=12) glucoside 3 3 10 5 Tetradecylamine oxide 1 1 | 3 5 | 5 Na alkyl (c=12) 1 5 3 10 benzenesulfonate 1 5 3 10 Polyoxyethylene (p=4) polyoxypropylene (p=2) 1 1 alkyl (c=12) ether Diethylene glycol 10 20 10 20 20 20 10 monobutyl ether Propylene glycol 10 20 10 10 monobutyl ether Monoethanolamine 5 5 10 5 5 Na carbonate 10 5 10 15 Water Bal Bal Bal Bal Bal Bal Bal Bal Detergency B B A A C B C B ≈ & Easiness of A A A A C C C C W wiping Remaining A A A A C B C C behavior Bal: Balance
Claims (11)
1. A detergent composition for hard surfaces, which comprises the following components (A), (B) and (C):
(A) a diphenyl ether disulfonate type anionic surfactant,
(B) a water-soluble solvent, and
(C) an amine compound.
2. A detergent composition for hard surfaces, which comprises the following components (A), (B) and (C):
(A) 0.01-20 wt.% of a diphenyl ether disulfonate type anionic surfactant,
(B) 0.1-50 wt.% of a water-soluble solvent, and
(C) 0.01-30 wt.% of an amine compound.
3. The detergent composition as claimed in claim 1 or 2, wherein the component (A) comprises one or more anionic surfactants selected from compounds represented by the following general formulae (1) and (2):
wherein R1 and R2 mean individually a linear or branched alkyl or alkenyl group having 5-15 carbon atoms, and M and
M' denote individually an alkali metal atom, an ammonium group or an alkanol-substituted ammonium group.
4. The detergent composition as claimed in claim 1 or 2, wherein the component (A) comprises one or more anionic surfactants selected from compounds represented by the following general formulae (1) and (2):
wherein R1 and R2 mean individually a linear or branched alkyl or alkenyl group having 5-15 carbon atoms, and M and
M' denote individually an alkali metal atom, an ammonium group or an alkanol-substituted ammonium group, the proportion of the compounds represented by said general formulae (1) and (2) being within a range of from 100/0 to 25/75 by weight.
5. The detergent composition as claimed in claim 1 or 2, wherein the component (B) comprises one or more watersoluble solvents selected from compounds represented by the following general formulae (3) through (5): R30(C2H40)m(C3H60)nR (3)
R70C(CH3)2(CH2CH20H (5) wherein R3 and R4 mean individually a hydrogen atom or an alkyl group having 1-8 carbon atoms, with the proviso that both groups R3 and R4 do not mean hydrogen atoms at the same time, m and n stand individually for an integer of 0-3, with the proviso that both m and n do not stand for integers of O at the same time, R5 and R6 denote individually an alkyl group having 1-3 carbon atoms, and R7 means an alkyl group having 1-3 carbon atoms, dihydric alcohols having 4-12 carbon atoms and monohydric alcohols having 1-5 carbon atoms.
6. The detergent composition as claimed in claim 1 or 2, wherein the component (B) comprises one or more watersoluble solvents selected from compounds represented by the following general formula (3'): R3,O(C2H4O)mi (C3H6O)nR4, (3') wherein R3 and R41 mean individually a hydrogen atom or an alkyl group having 1-4 carbon atoms, with the proviso that both groups R3 and R4 do not mean hydrogen atoms at the same time, and m' and n' stand individually for an integer of 0-3, with the proviso that both m' and n' do not mean 0 at the same time, m' does not denote 1 and n' does not mean 0.
7. The detergent composition as claimed in claim 1 or 2, wherein the component (C) comprises one or more amine compounds selected from compounds represented by the following general formulae (6) through (9):
wherein R8, R11, R131 R15, R17 R19 and R20 mean individually a hydrogen atom or an alkyl group having 1-4 carbon atoms, and R9, R10, R12, R14, R16 and R18 denote individually a hydrogen atom, an alkyl group having 1-4 carbon atoms or a hydroxyalkyl group having 2-3 carbon atoms.
8. The detergent composition as claimed in any one of claims 1-6, which further comprises, as a component (D), 0.01-20 wt.% of at least one surfactant other than the component (A).
9. The detergent composition as claimed in claim 8, wherein the component (D) comprises one or more surfactants selected from higher fatty acid alkanolamides or their addition products with alkylene oxides, amine oxides, alkylglycosides, sulfobetaines and carbobetaines.
10. The detergent composition as claimed in claim 8, wherein the component (D) comprises one or more alkylglycosides represented by the following general formula (10): R21(OR22)xGy (10) wherein R21 means a linear or branched alkyl, alkenyl or alkylphenyl group having 8-18 carbon atoms, R22 denotes an alkylene group having 2-4 carbon atoms, G represents a residue derived from a reducing sugar having 5-6 carbon atoms, x stands for a number of 0-5 in terms of the average value, and y means a number of 1-10 in terms of the average value.
11. Detergent composition substantially as described in the Examples.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33068292 | 1992-12-10 | ||
JP5084754A JP2521630B2 (en) | 1992-12-10 | 1993-04-12 | Cleaning composition for hard surfaces |
Publications (3)
Publication Number | Publication Date |
---|---|
GB9310677D0 GB9310677D0 (en) | 1993-07-07 |
GB2273300A true GB2273300A (en) | 1994-06-15 |
GB2273300B GB2273300B (en) | 1997-03-26 |
Family
ID=26425744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9310677A Expired - Fee Related GB2273300B (en) | 1992-12-10 | 1993-05-24 | Detergent composition for hard surfaces |
Country Status (6)
Country | Link |
---|---|
JP (1) | JP2521630B2 (en) |
GB (1) | GB2273300B (en) |
HK (1) | HK1000165A1 (en) |
MY (1) | MY110901A (en) |
SG (1) | SG46181A1 (en) |
TW (1) | TW230783B (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0623669A2 (en) * | 1993-05-03 | 1994-11-09 | The Procter & Gamble Company | Liquid hard surface detergent compositions containing amphoteric detergent surfactant and specific anionic surfactant |
WO1997006229A1 (en) * | 1995-08-08 | 1997-02-20 | Henkel Corporation | Metal cleaning composition and process that do not damage plastic |
EP0964056A2 (en) * | 1998-06-08 | 1999-12-15 | Ecolab Inc. | Compositions and process for cleaning and finishing hard surfaces |
EP1341882A1 (en) * | 2000-11-24 | 2003-09-10 | Henkel KGaA | Mixed surfactant cleaning compositions with reduced streaking |
WO2009024747A2 (en) * | 2007-08-17 | 2009-02-26 | Reckitt Benckiser Inc. | Environmentally acceptable hard surface treatment compositions |
US10570355B2 (en) | 2015-06-24 | 2020-02-25 | Kao Corporation | Cleaning agent composition for glass hard disk substrate |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06346094A (en) * | 1993-06-02 | 1994-12-20 | Kuraray Co Ltd | Non-flammable cleanser composition |
US6528478B2 (en) | 2000-10-16 | 2003-03-04 | Takatushi Totoki | Cleaning chemical composition comprising an amine oxide, alkanolamine, and organic solvent |
JP4429001B2 (en) * | 2003-12-15 | 2010-03-10 | ライオン株式会社 | Multipurpose liquid detergent composition |
CN109715775A (en) * | 2016-09-23 | 2019-05-03 | 狮王株式会社 | Liquid detergent |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0040882A1 (en) * | 1980-05-27 | 1981-12-02 | THE PROCTER & GAMBLE COMPANY | Liquid detergent compositions |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ210848A (en) * | 1984-08-29 | 1988-06-30 | Ecolab Inc | Mechanical dishwashing rinse composition containing low foaming sulphonic acid rinsing agent and source of active halogen |
JPS6191299A (en) * | 1984-10-12 | 1986-05-09 | 川研ファインケミカル株式会社 | Hard surface cleanser |
JPH0715111B2 (en) * | 1986-05-01 | 1995-02-22 | 花王株式会社 | Glass cleaner composition |
AU4702289A (en) * | 1989-01-19 | 1990-07-26 | Sterling Drug Inc. | Hard surface cleaning composition |
-
1993
- 1993-04-12 JP JP5084754A patent/JP2521630B2/en not_active Expired - Fee Related
- 1993-05-04 TW TW082103493A patent/TW230783B/zh not_active IP Right Cessation
- 1993-05-24 SG SG1996000242A patent/SG46181A1/en unknown
- 1993-05-24 GB GB9310677A patent/GB2273300B/en not_active Expired - Fee Related
- 1993-06-18 MY MYPI93001182A patent/MY110901A/en unknown
-
1997
- 1997-08-22 HK HK97101678A patent/HK1000165A1/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0040882A1 (en) * | 1980-05-27 | 1981-12-02 | THE PROCTER & GAMBLE COMPANY | Liquid detergent compositions |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0623669A2 (en) * | 1993-05-03 | 1994-11-09 | The Procter & Gamble Company | Liquid hard surface detergent compositions containing amphoteric detergent surfactant and specific anionic surfactant |
EP0623669A3 (en) * | 1993-05-03 | 1995-07-26 | Procter & Gamble | Liquid hard surface detergent compositions containing amphoteric detergent surfactant and specific anionic surfactant. |
WO1997006229A1 (en) * | 1995-08-08 | 1997-02-20 | Henkel Corporation | Metal cleaning composition and process that do not damage plastic |
EP0964056A2 (en) * | 1998-06-08 | 1999-12-15 | Ecolab Inc. | Compositions and process for cleaning and finishing hard surfaces |
EP0964056A3 (en) * | 1998-06-08 | 2000-01-05 | Ecolab Inc. | Compositions and process for cleaning and finishing hard surfaces |
EP1341882A1 (en) * | 2000-11-24 | 2003-09-10 | Henkel KGaA | Mixed surfactant cleaning compositions with reduced streaking |
EP1341882A4 (en) * | 2000-11-24 | 2004-09-01 | Henkel Kgaa | Mixed surfactant cleaning compositions with reduced streaking |
WO2009024747A2 (en) * | 2007-08-17 | 2009-02-26 | Reckitt Benckiser Inc. | Environmentally acceptable hard surface treatment compositions |
WO2009024747A3 (en) * | 2007-08-17 | 2009-04-09 | Reckitt Benckiser Inc | Environmentally acceptable hard surface treatment compositions |
US10570355B2 (en) | 2015-06-24 | 2020-02-25 | Kao Corporation | Cleaning agent composition for glass hard disk substrate |
Also Published As
Publication number | Publication date |
---|---|
GB9310677D0 (en) | 1993-07-07 |
TW230783B (en) | 1994-09-21 |
SG46181A1 (en) | 1998-02-20 |
JP2521630B2 (en) | 1996-08-07 |
HK1000165A1 (en) | 1998-01-09 |
GB2273300B (en) | 1997-03-26 |
JPH06228591A (en) | 1994-08-16 |
MY110901A (en) | 1999-06-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4396520A (en) | Detergent compositions | |
US5507970A (en) | Detergent composition | |
EP0698660B1 (en) | Detergent composition for hard surface | |
JP4864598B2 (en) | Cleaning composition for hard surface | |
GB2273300A (en) | Hard surface cleaning compositions | |
US6897187B2 (en) | Light duty liquid cleaners comprising a monoalkoxylated quaternary ammonium surfactant | |
JP2952561B2 (en) | Bathroom cleaning composition | |
US7375067B2 (en) | Liquid detergent composition comprising an anionic surfactant, amine oxide, and alkyl glyceryl ether | |
US5096621A (en) | Detergent composition containing di-long chain alkyl amine oxides | |
JP4176325B2 (en) | Liquid detergent composition | |
JP3213467B2 (en) | Cleaning composition for hard surfaces | |
JPH11256200A (en) | Liquid detergent composition | |
JPH0699711B2 (en) | Liquid detergent composition | |
JP4864222B2 (en) | Liquid detergent composition for hard surfaces | |
JP3205655B2 (en) | Cleaning composition for hard surfaces | |
JP3751420B2 (en) | Cleaning composition for hard surface | |
JP3625957B2 (en) | Cleaning composition for hard surface | |
US6187731B1 (en) | Cleaning compositions for hard surfaces containing naphthalene sulfonic acid/formaldehyde condensates | |
JP3174658B2 (en) | Liquid detergent composition | |
JP2952555B2 (en) | Hard surface cleaning composition | |
JPH04292696A (en) | Liquid foamy detergent having high viscosity | |
EP0576691B1 (en) | Detergent composition | |
JPH05331454A (en) | Anti-fogging agent | |
JPH05279695A (en) | Detergent composition for hard surface | |
JPH10219292A (en) | Detergent composition for hard surface |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20100524 |