IE853191L - Detergent compositions - Google Patents
Detergent compositionsInfo
- Publication number
- IE853191L IE853191L IE853191A IE319185A IE853191L IE 853191 L IE853191 L IE 853191L IE 853191 A IE853191 A IE 853191A IE 319185 A IE319185 A IE 319185A IE 853191 L IE853191 L IE 853191L
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- Ireland
- Prior art keywords
- detergent
- weight
- detergent composition
- composition
- water
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Classifications
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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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2082—Polycarboxylic acids-salts thereof
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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
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers 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
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
Abstract
The composition comprises (a) from 15 to 18%, by weight, of a water-soluble non-phosphate detergent builder salt; (b) from 15 to 23%, by weight, of a surface active nonionic detergent compound which is the condensation product of 5 to 9 moles of ethylene oxide with one mole of a C12-15 aliphatic alcohol. (c) from 1 to 6%, by weight of at least one amphoteric detergent compound selected from betaine detergent compounds; (d) from 5 to 8%, by weight, of a solubilizer selected from alkali metal salts of nonyl succinic or nonyl maleic anhydride; and (e) from 35 to 65%, by weight, water. m
Description
.8 69 9 PI2 591 la "CONCENTRATED SINGLE-PHASE BUILT LIQUID DETERGENT COMPOSITION" The present invention relates to concentrated aqueous, built liquid detergent compositions suitable for laundry or pre-soak formulations. More particularly, it relates to aqueous built liquid detergent 5. compositions which are highly concentrated in surfactant and builder and are provided as homogeneous, clear single-phase liquid solutions.
The formulation of concentrated built aqueous liquid detergent compositions has been a commercial 10. objective in the detergent art in recent years. It is generally required that such compositions provide good detergency at low product concentration in the bath, contain water as the principal solvent and are in the form of homogeneous single-phase solutions 15. which provide long-term shelf life without undergoing phase separation. Conventional liquid detergent compositions containing a detergency builder are generally not highly concentrated. That is, they are formulated as relatively dilute aqueous solutions so 20. as to solubilize the builder and surfactant in the liquid composition. To provide the desired detergency, relatively high concentrations of such product are needed in the bath.
The term "concentrated" as used herein refers to 25. liquid detergent compositions which can provide effective detergency at a product concentration equivalent to about "l/4 cup" under U.S. washing conditions, namely about 60 ml of detergent composition per standard wash load (about 17 U.S. gallons 30. (64 litres) for a top loading washing machine), which P12591 corresponds to a concentration of about 0.1% of the liquid detergent composition in the wash bach. To achieve a commercially aceptable level of detergency at such low product concentration, it is necessary 5. that a high proportion of the detergent composition be comprised of active ingredients, notably, surfactant and builder. Thus, the term "concentrated" liquid detergent as used herein, is defined as a detergent composition which contains no more than 10. about 65%, by weight, of water.
As a practical matter, it is important that water is used as the principal, if not the sole, solvent in such concentrated liquid detergent composition, avoiding the use of costly solvents such as 15. glycols. Accordingly, the liquid detergent compositions described herein contain at a minimum about 35% water, by weight of the liquid composition, a water content of about 45% to 60% being ordinarily preferred. 20. Built liquid detergent compositions are known in the art. However, because of the limited solubility of builder and surfactant in water, such detergent compositions are generally prepared as relatively dilute aqueous compositions containing for the most 25. part in excess of 65%, and often as high as 93%, by weight, water. Frequently, an alkylene glycol co-solvent is used to enhance the solubility of the built detergent composition. In those aqueous compositions which contain less than 65% water, the 30. proportion of builder is generally kept low, i.e. no P12591 greater than about 10%, by weight, so as to enhance the solubility of the built detergent in water. To provide acceptable detergency when used under standard U.S. washing conditions, such known liquid 5. compositions are conventionally used at product concentrations substantially above the "1/4 cup" concentration (about 0.1%, by weight) at which the liquid detergent compositions of the present invention are effective. Moreover, the conventional 10- detergent compositions are generally in the form of emulsions or suspensions rather than forming clear homogeneous solutions which are stable against phase separation.
The detergent compositions described in U.S. 15. Patent No. 3,912,662 to Martinsson et al and U.S. Patent No. 4,021,377 to Borchert et al are illustrative of the prior art. The Martinsson et al patent discloses an aqueous detergent composition containing nonionic and betaine detergents and a poly-20. phosphate builder. In Example 1, a composition is described containing 66% water and 12% alkylene glycol as the solvent. The Borchert et al patent describes a phosphate-free liquid detergent composition containing citrate builder and surfactant in a 25. water-glycol solvent. The amount of water in each of the seven compositions disclosed in Table 1 of the patent is less than 26%, by weight, the major portion of the solvent being an alkylene glycol.
Consequently, the ability to provide an economical 30. liquid detergent composition which utilizes water as P12591 4. the principal solvent yet is in the form of a concentrated clear single-phase solution remains as a problem yet to be overcome in formulating a commercially acceptable built concentrated liquid 5. detergent composition.
The present invention provides a concentrated aqueous single-phase homogeneous built liquid detergent composition comprising: (a) from about 15 to 18%, by weight, of a 10. water-soluble non-phosphate detergent builder salt; (b) from about 15 to 23%, by weight, of a surface active nonionic detergent compound which is the condensation product of 5 to 9 moles of 15. ethylene oxide with one mole of an aliphatic alcohol containing 12 to 15 carbon atoms; (c) from about 1 to 6%, by weight, of at least one amphoteric detergent compound selected from the group consisting of 20. (i) betaine detergent compounds having the structure: R2 25. 30.
R1—CH2—N+—R4—COO-; and R3 (ii) alkyl amido betaine detergent compounds having the structure: O R2 R1—C—NH—R5—N+—R4—COO" R- P12591 5 . wherein R1 represents an alkyl group or a mixture of alkyl groups containing 9 to 13 carbon atoms, R2 and R3 each independently represent a methyl or an ethyl group, and and 5 r5 each independently represent a methylene, ethylene or propylene radical; (a) from about 5 to 8%. by weight, of a solubilizer selected from the group consisting of alkali metal salts of (i) nonyl succinic 10 anhydride and (ii) nonyl maleic anhydride; and (e) from about 35 to 65%, by weight, water. In accordance with the process aspects of the present invention, laundering of stained and/or soiled materials is effected by contacting such 15 materials with an aqueous solution of the above-defined liquid detergent composition.
Unlike the built liquid detergent compositions known in the art, the compositions of the present invention contain a high concentration of builder and 20 surfactant yet are characteristically clear, single-phase homogeneous solutions which are physically stable over prolonged periods of storage and over a wide range of temperature. The particular combinations of nonionic and betaine detergents with non-25 phosphate builder salt and solubilizer in accordance with the present invention unexpectedly form clear single-phase aqueous solutions, highly concentrated in both surfactant and builder. From a commercial standpoint, the compositions of the present invention 30 are particularly advantageous insofar as they are 35 P12591 phosphate-free in conformity with governmental regulations in many areas which prohibit the use of phosphate-containing detergents; they are relatively economical to formulate in that they utilize water as 5. the principal solvent and avoid the use of costly co-solvents such as alkylene glycols in other than minor amounts; they provide effective detergency at low product concentrations in the wash bath, notably at a so-called l/4 cup concentration, a desirably low 10. concentration under U.S. washing conditions; and they are homogeneous solutions, avoiding problems of non-uniformity and phase separation associated with the storage and use of emulsions and dispersions.
The nonionic detergent compound in the liquid 15. detergent compositions of the present invention may constitute from about 15 to 23%, and preferably from 17 to 19%, by weight, of the detergent composition, and the amphoteric detergent compound will generally vary from about 1 to 6%, preferably from 2 to 4%, by 20. weight, of such compositions. The relative amounts of each of the aforementioned detergents is generally determined by the amount of builder salt employed. The higher the builder concentrations within the range of 15 to 18%, the lower the maximum concentra-25. tion of nonionic detergent which may be employed in the composition and still form a stable single-phase solution. Conversely, at higher concentrations of builder salt, the concentration of amphoteric detergent and solubilizer is preferably increased within 30. the ranges of concentration set forth above so as to P12591 solubilize the mixture and form a clear sinale-phase solution having the requisite detergency. Thus, for example, at a builder concentration of about 17% or above, the preferred concentration of nonionic 5. surfactant is from about 1G to 18%, the amphoteric detergent is from about 2 to 4%, and most desirably at least 3%, and the concentration of solubilizer is about 7 to 8%, all percentages being by weight of the total composition. 10. The synthetic nonionic detergent employed in the practice of the present invention is specific to those compounds which are the condensation product of 5 to 9 moles of ethylene oxide with an aliphatic alcohol containing 12 to 15 carbon atoms. The 15. aliphatic alcohol is preferably a straight chain alcohol, and most preferably is a fatty alcohol or mixture thereof containing an average of 12 to 13 carbon atoms per mole. The number of ethylene oxide groups per mole of alcohol preferably averages about 20. 6.5 or 7. Neodol (Registered Trade Mark) 23-6.5 and Neodol (Registered Trade Mark) 25-7 are particularly preferred for use herein, both of such products being made by Shell Chemical Company, Inc.
The amphoteric detergent compounds most useful 25. in the compositions of the present invention are the betaine and alkyl amido betaine detergent compounds having the following structures: (i) betaine R2 30 - | ^ Rl—CH2—N+—g00~; and P12591 8 . (ii) alkyl amido betaine 0 R2 II I Rl—C — NH—R5—N + —R4—COO" R3 wherein in each of the above structures R^ represents an alkyl chain or a mixture of alkyls containing 9 to 13 carbon atoms; R2 and R3 each independently represent a methyl or an ethyl group,- and R4 and R^ each independently represent a methylene, ethylene or propylene radical.
When Rl is a mixture of alkyls of varying chain length, it is preferred that such mixture be comprised predominantly of alkyls having 9 to 13 carbon atoms, although it is sufficient, albeit less preferred, if only the predominant alkyl in the mixture contains 9 to 13 carbon atoms and the remaining alkyl chains are outside of such range. Rl is preferably derived from coconut oil.
R2 and R3 are preferably methyl groups and R4 is preferably a methylene group and R5 is preferably a propylene radical. Accordingly, preferred betaines for use herein are cocodimethyl- ammonium acetate (cocobetaine) and cocoamidopropyl dimethylammonium acetate (cocoamido betaine).
An anionic detergent may optionally be employed in minor amounts to supplement the nonionic and amphoteric detergent compounds in the liquid deter- P12591 9. gent compositions of the present invention.
Generally, the amount of anionic detergent will be below aoout 3%, by weight, of the total composition because of the limited solubility of such detergents in the built liquid detergent composition. Alkyl benzene sulphonate salts wherein the alkyl group contains 10 to 18 carbon atoms are particularly limited in solubility in the compositions of the present invention, and hence it is preferred that the lo. compositions of the present invention be substantially free of such compounds to avoid the possibility of product separation.
The preferred anionic detergents for use herein are sulphated ethoxylated higher fatty alcohols of 15^ the formula R0(C2H40)mS03M wherein R represents a fatty alkyl group of from 10 to 18 or 20 carbon atoms, m is from 2 to & or 8 (preferably having a value from about 1/5 to l/2 the 20. number of carbon atoms in R) and M is a solubilizing salt-forming cation, such as an alkali metal, ammonium, lower alkyl-amino or lower alkanolamino. A preferred polyethoxylated alcohol sulphate detergent is available from Shell Chemical Company and is 25 marketed as Neodol 25-3S.
Water is the principal solvent in the concentrated liquid detergent compositions of the present invention. The concentration of water may vary from about 35 to 65%, with a concentration in the range of 30 45 to 60%, by weight, being generally preferred. A P12591 10. co-solvent such as an alkylene glycol, e.g. ethylene glycol or propylene glycol, may optionally be employed in minor amounts for the purpose of enhancing the solubility of the surfactant and the 5. builder in solution. The concentration of alkylene glycol in the detergent composition should, if present, be below about 10%, by weight, of the total composition, preferably below about 5%, and most preferably, the composition is substantially free of 10. such alkylene glycol.
One or more alkali metal salts of nonyl succinic anhydride or nonyl maleic anhydride are included in the detergent composition because of their solubilizing properties with respect to 15. nonionic surfactants and builder salts. Such solubilizer is used in an amount of from 5 to 8%, by weight, of the total composition, a concentration of at least 7% being preferred when the builder salt concentration is about 17% or higher. 20. The term nonyl succinic anhydride as used herein means a compound having the formula H O 25. C9—C— ^O H-C—C' H O 30. wherein C9 represents a nine carbon atom member P12591 11. 10. aliphatic chain, preferably an alkyl chain. Nonyl maleic anhydride is similarly defined, the structures of succinic and maleic anhydride differing only by virtue of the unsaturated nature of maleic acid; the formula for nonyl maleic anhydride as used herein being: 0 '9 c C 0 H-C- O 15„ The non-phosphate detergent builder salts are employed in the present compositions in amounts generally of from about 15 to 18%, by weight.
Specific examples of non-phosphate water-soluble inorganic builders include water-soluble inorganic 20. carbonate, bicarbonate and silicate salts. The alkali (for example, sodium and potassium) carbonates, bicarbonates and silicates are particularly useful herein.
Water-soluble organic builders are also useful 25. and include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxysulphonates.
Specific examples of polyacetate and polycarboxylate builders include sodium, potassium, lithium, ammonium 30. and substituted ammonium salts of ethylene diamine- P12591 12 . tetracetic acid, nitrilotriacetic acid, benzene poly-carboxylic (i.e. penta- and tetra-) acids, carboxy-methoxysuccinic acid and citric acid. As used herein, the term "builder" does not include surfactants and soaps such as the water-soluble salts of higher fatty acids containing from about 8 to 20 carbon atoms.
The optical fluorescent brighteners or whiteners often employed in the liquid detergent compositions are important constituents of modern detergent compositions which give washed laundry and materials a bright appearance so that the laundry is not only clean but also appears clean. Although it is possible to utilize a single brightener for a specific intended purpose in the liquid detergent compositions of the present invention it is generally desirable to employ mixtures of brighteners which will have good brightening effects on cotton, nylons, polyesters and blends of such materials and which are also bleach stable. A good description of such types of optical brighteners is given in the article "The Requirements of Present day Detergent Fluorescent Whitening Agents" by A.E. Siegrist, J. Am. Oil Chemists Soc., January 1978 (Vol. 55). That article and U.S. Patent 3,812,041, issued 21st May, 1974, contain detailed descriptions of a wide variety of suitable optical brighteners.
Among the brighteners that are useful in the liquid detergent compositions of the present 13. invention are: Calcofluor 5 BM (American Cyanamid); Tinopal (Registered Trade Mark) LPW (Ciba); SOF A-2001 (Ciba); CDW (Hilton- Davis); Phorwite RKH, Phorwhite BBH and Phorwite BHC (Verona); CSL, powder, acid (American Cyanamid); FB 766 (Verona); Blancophor PD (GAF); CJNPA (Geigy); Tinopal RBS 200 (Geigy).
Adjuvants may be present in the liquid detergent compositions to provide additional properties, either functional or aesthetic. Included among the useful adjuvants are soil suspending or anti-redeposition agents, such as polyvinyl alcohol, sodium carboxy-methyl cellulose, hydroxypropylmethy1 cellulose; thickeners, e.g. gums, alginates, agar agar; foam improvers, e.g. lauric myristic diethanolamide; foam destroyers, e.g. silicones; bactericides, e.g. tribromosalicylanilide, hexachlorophene; dyes; pigments (water dispersible); preservatives; ultraviolet absorbers; fabric softeners; enzymes; opacifying agents, e.g. polystyrene suspensions; and perfumes. Of course, such materials will be selected based on the properties desired in the finished product, their compatbility with the other constituents, and their solubility in the liquid composition.
The liquid compositions of the present invention are efficient and easy to use. Compared to heavy duty laundry detergent powders, much smaller volumes of the liquids of the present invention are employed to obtain comparable cleaning of soiled laundry. For example, using a typical preferred formulation of the P12 59 1 14. present invention, only about 71 grams or l/4 cup of liquid is needed for a full tub of wash in a top-loading automatic washing machine in which the water volume is about 17 gallons (about 64 litres); and 5. even less is needed for front-loading machines.
Thus, the concentration of the liquid detergent composition in the wash water is of the order of about 0.1%. Usually, the proportion of the liquid composition in the wash solution will range from 10. about 0.05 to 0.3%, preferably from 0.10 to 0.20%. The proportions of the various constituents of the liquid composition may vary accordingly. Equivalent results can be obtained by using greater proportions of a more dilute formulation but the greater quantity 15. needed will require additional packaging and will generally be less convenient for consumer use.
The invention may be put into practice in various ways and a number of specific embodiments will be described to illustrate the invention with 20. reference to the accompanying examples.
EXAMPLE 1 A concentrated built liquid detergent composition in accordance with the present invention was formulated as set forth in Table 1 below. The 25. percentages shown refer to the 100% active component.
P12591 15. table 1 COMPONENT Sodium Citrate Ethoxylated C-^-C^ alcohol (6.5 WEIGHT PERCENT 17.2 17.6 5. moles EO/mole alcohol) Cocoamido betaine^-*-) Nonyl succinic anhydride^) 3.1 7.0 (Potassium salt) Brightener and blue dye 0.2 10. Water Balance Notes on Table 1 (1) Provided as "Varion CADG", an aqueous solution of cocoamido betaine sold by Sherex Chemical Company. 15. (2) The anhydride is provided as "Hoe 2817" sold by 20. clear blue-coloured single-phase homogeneous liquid detergent having a viscosity of about 80 centipoise (cp) at 75°F (24°C), and which poured satisfactorily from a plastic detergent bottle with a discharge opening of about 2.5 cm diameter. The liquid 25. detergent was employed to wash a mixed load of soiled laundry which included cotton swatches and polyester/ cotton swatches soiled with particulate soil and with sebum soil. The wash temperature was 120°F (49°C) and the concentration of the liquid detergent in the 30. wash bath was about 0.1%, by weight. After washing, American Hoechst Company, which is then reacted with potassium hydroxide to form the potassium salt.
The above-described liquid composition was a P12591 16. the laundered items were rinsed in tap water and then dried. The degree of stain removal was measured by taking a reflectance reading for each stained test swatch prior to and after the washing using a Gardner 5. XL-20 colourimeter.
The laundering operation described above was repeated with a control detergent, a commercial aqueous built liquid detergent composition containing 19% dodecylbenzene sulphonate, 10% sodium citrate, 7% 10. ethoxylated alcohol surfactant, and 5% sodium toluene sulphonate hydrotrope used at a "l/2 cup" concentration of about 0.2%, by weight, in the bath. The detergency of both compositions was compared based on the measured stain removal achieved during laundering. 15. The detergency of the liquid detergent of the present invention at a "1/4 cup" concentration was shown to be either equivalent to or superior to that achieved with the control liquid detergent at a "l/2 cup" concentration with respect to laundered soiled and 20. stained fabrics.
EXAMPLES 2A and 2B The effect of incorporating a betaine detergent not in accordance with the present invention into a built liquid detergent composition containing 25. nonionic surfactant and a high concentration of builder was demonstrated by preparing two liquid compositions as described in Example 1, except that the cocoamido betaine in the composition of Example 1 was replaced in one composition by stearyl betaine 30. (Example 2A) and in the second composition by palmytyl P12591 17. betaine (Example 2B). Both of the resulting compositions were unstable and formed separate phases in contrast to the stable clear solution which characterised the composition of Example 1. 5. EXAMPLES 3A, 3B and 3C Detergency tests were conducted with compositions A, B and C formulated as shown in Table 2 below. The numbers in Table 2 represent the percent by weight of each component in the liquid composition. 10 . TABLE 2 EXAMPLE 3A 3B 3C COMPONENT Sodium citrate 17.2 17.2 17.2 Ethoxylated Ci2_c13 alcohol 17.6 22.0 7.0 15. (6.5 moles EO/mole alcohol) Cocoamido betaine 3.1 — 9.0 Nonyl succinic anhydride 7.0 14.0 — (potassium salt) Water Balance Balance Balance 20.
All three compositions were clear, single-phase solutions. The composition of Example 3A is a composition in accordance with the present invention substantially as previously described in Example 1. 25. The composition of Example 33 represents the best performing formulation from the standpoint of detergency measured at a concentration of 0.1% in the bath from among compositions containing the same components of the composition of Example 3A except 30. for the omission of a betaine detergent, and which P12591 18 . formed a clear single-phase solution. Similarly, the composition of Example 3C represents the best performing formulation from the standpoint of detergency measured at a concentration of 0.1% in the 5 bath from among compositions containing the same components of Composition A, but which contained no solubilizer, and which formed a clear single-phase solution. The compositions of Examples 33 and 3C are not in accordance with the present invention and are 10 comparison examples.
The detergency of the composition of Examples 3A, 3B and 3C was determined in a Tergotometer vessel manufactured by U.S. Testing Company on the test fabrics and under the conditions stated in Table 3 15 below: TABLE 3 TEST FABRICS TFN - Test fabric soil on Nylon PCC - Piscataway clay on cotton 20 SC - Sebum particulate on cotton SDC - Sebum particulate on Dacron (Registered Trade Mark)/cotton EMPA - EMPA 101 on heavy cotton WASH CONDITIONS 25 Liquid detergent concentration 0.10% Water temperature 120JF (49°C) Water hardness about 150 ppm as calcium carbonate 30 At the end of the wash, the test swatches were rinsed in tap water and then dried. A reflectance P12591 19. reading was taken for each test swatch prior to and after the washing using a Gardner XL-20 colourimeter.
The values for the change in reflectance (ARd) are shown below in Table 4 for each of the aforementioned 5. test fabrics. A difference greater than 0.8 between two values of ARd is considered significant for all washed test fabrics except for measurements on EMPA where only ARd values above 1.3 are considered significant. 10. table 4 ARd Values for Fabrics Washed with Compositions A, B and C fabric tfn pcc empa sc sdc example 15. 3A 37 24 18 10 44 3B 35 24 17 8 42 3C 29 21 15 4 34 Table 4 demonstrates the unexpected improved 20. detergency attendant on the use of a composition in accordance with the present invention relative to two single-phase liquid detergent compositions similar thereto but which were not formulated in accordance with the present invention. The composition of 25. Example 3A is shown to be superior to the composition of Example 3b with respect to the majority of test fabrics laundered; and superior to the composition of Example 3C with respect to virtually all the test fabrics laundered above. 30.
P12591 20.
Claims (15)
1. A concentrated aqueous single-phase homogeneous built liquid detergent composition comprising: (a) from about 15 to 18%, by weight, of a water-soluble non-phosphate detergent builder salt; 5. (b) from about 15 to 23%, by weight, of a surface active nonionic detergent compound which is the condensation product of 5 to 9 moles of ethylene oxide with one mole of an aliphatic alcohol containing 12 to 15 carbon atoms; 10. (c) from about 1 to 6%, by weight, of at least one amphoteric detergent compound selected from the group consisting of (i) betaine detergent compounds having the structure: 15. R2 R1—CH2—N+—R4—COO-; and R3 20. (ii) alkyl amido betaine detergent compounds having the structure: O R2 25. R1—C—NH—r5—N+—R4—COCT .3 R* wherein R^- represents an alkyl group or a mixture of alkyl groups containing 9 to 13 carbon 30. P12591 21. atoms, R2 and R3 each independently represent a methyl or an ethyl group and R4 and R^ each independently represent a methylene, ethylene or propylene radical; 5 (d) from about 5 to 8%, by weight, of a solubilizer selected from the group consisting of alkali metal salts of (i) nonyl succinic anhydride (as defined herein) and (ii) nonyl maleic anhydride (as defined herein); and 10. (e) from about 35 to 65%, by weight, water.
2. A detergent composition as claimed in Claim 1 in which the said nonionic detergent compound is the condensation product of 6 to 7 moles of ethylene 15oxide with one mole of an aliphatic alcohol containing 12 to 13 carbon atoms.
3. A detergent composition as claimed in Claim 1 or Claim 2 in which the said builder salt is sodium 20 citrate.
4. A detergent composition as claimed in Claim 1, 2 or 3 in which in the structures of the said betaine detergent compounds is derived from coconut 25 oil, R2 and R3 each represent a methyl group, and R4 represents a methylene radical.
5. A detergent composition as claimed in any one of Claims 1 to 4 in which the said betaine 30. detergent compound is cocoamidopropyldimethyl ammonium acetate. PI 2591 22.
6. A detergent composition as claimed in any one of Claims 1 to 5 which contains less than about 3%, by weight, of a surface active anionic detergent compound. 5.
7. A detergent composition as claimed in any one of Claims 1 to 6 which is substantially free of a CjL0~Ci8 alkyl benzene sulphonate anionic detergent.
8. 10. 8. A detergent composition as claimed in any one of Claims 1 to 7 which contains less than about 10%, by weight, of an alkylene glycol.
9. A detergent composition as claimed in any 15. one of Claims 1 to 8 which is substantially free of an alkylene glycol.
10. A detergent composition as claimed in any one of Claims 1 to 9 which contains from about 45 to 20. 60%, by weight, of water.
11. A detergent composition as claimed in any one of Claims 1 to 10 in which the concentration of the builder salt is about 17% and the nonionic 25. detergent compound is present in an amount of from about 16 to about 18%, by weight, of the composition.
12. A detergent composition as claimed in any one of Claims 1 to 11 in which the concentration of 30. the said solubilizer in the composition is about 7%, by weight. P12591 23.
13. A detergent composition as claimed in Claim 1 substantially as specifically described herein with reference to Example 1 or Example 3A.
14. A method of laundering comprising contacting the stained and/or soiled fabrics to be laundered with a concentrated aqueous single-phase homogeneous liquid detergent composition as claimed in any one of Claims 1 to 13.
15. A method as claimed in Claim 14 in which the concentration of detergent composition in the wash water is about 0.1%, by weight. Dated this 17th day of December 1985 (signed) 5 Dartmouth Road Dublin 6.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US68297184A | 1984-12-18 | 1984-12-18 |
Publications (2)
Publication Number | Publication Date |
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IE853191L true IE853191L (en) | 1986-06-18 |
IE58699B1 IE58699B1 (en) | 1993-11-03 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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IE319185A IE58699B1 (en) | 1984-12-18 | 1985-12-17 | Concentrated single-phase built liquid detergent composition |
Country Status (32)
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JP (1) | JPS61145298A (en) |
KR (1) | KR930003937B1 (en) |
AR (1) | AR240336A1 (en) |
AT (1) | AT394378B (en) |
AU (1) | AU578333B2 (en) |
BE (1) | BE903874A (en) |
BR (1) | BR8506327A (en) |
CA (1) | CA1255182A (en) |
CH (1) | CH668078A5 (en) |
DE (1) | DE3544236A1 (en) |
DK (1) | DK160771C (en) |
EG (1) | EG17366A (en) |
FI (1) | FI79135C (en) |
FR (1) | FR2574813B1 (en) |
GB (1) | GB2170816B (en) |
GR (1) | GR853046B (en) |
HK (1) | HK41191A (en) |
IE (1) | IE58699B1 (en) |
IN (1) | IN165674B (en) |
IT (1) | IT1182083B (en) |
LU (1) | LU86213A1 (en) |
MX (1) | MX162411A (en) |
NL (1) | NL8503482A (en) |
NO (1) | NO165926C (en) |
NZ (1) | NZ214410A (en) |
PH (1) | PH24520A (en) |
PT (1) | PT81670B (en) |
SE (1) | SE466262B (en) |
TR (1) | TR23505A (en) |
ZA (1) | ZA859267B (en) |
ZM (1) | ZM9885A1 (en) |
ZW (1) | ZW22085A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8511303D0 (en) * | 1985-05-03 | 1985-06-12 | Procter & Gamble | Liquid detergent compositions |
IN169730B (en) * | 1986-02-19 | 1991-12-14 | Ciba Geigy Ag | |
US4908147A (en) * | 1986-02-19 | 1990-03-13 | Ciba-Geigy Corporation | Aqueous self preserving soft contact lens solution and method |
FR2603601B1 (en) * | 1986-09-08 | 1988-11-10 | Lesieur Cotelle | COMPOSITION FOR CLEANING SANITARY FACILITIES |
US4830782A (en) * | 1987-08-31 | 1989-05-16 | Colgate-Palmolive Company | Hot water wash cycle built nonaqueous liquid nonionic laundry detergent composition containing amphoteric surfactant and method of use |
US4900467A (en) * | 1988-05-20 | 1990-02-13 | The Clorox Company | Viscoelastic cleaning compositions with long relaxation times |
US5063084A (en) * | 1990-05-31 | 1991-11-05 | Nelson Riley H | Method of preventing adherence of insect residues to vehicular surfaces |
EP0476212A1 (en) * | 1990-09-17 | 1992-03-25 | The Procter & Gamble Company | Liquid detergent compositions |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3579453A (en) * | 1968-11-12 | 1971-05-18 | Rohm & Haas | Alkali-soluble surfactant consisting of substituted succinic acid-nonionic ethoxylate blends |
SE380751B (en) * | 1971-11-12 | 1975-11-17 | Seco Tools Ab | FRIENDS |
FR2327310A1 (en) * | 1972-11-30 | 1977-05-06 | Modokemi Ab | LIQUID DETERGENT COMPOSITION |
US4122043A (en) * | 1973-12-19 | 1978-10-24 | Polytrol Chemical Corporation | Amidobetaine containing detergent composition non-toxic to aquatic life |
AT344301B (en) * | 1974-08-01 | 1978-07-10 | Hoechst Ag | CLEANING SUPPLIES |
CA1115618A (en) * | 1977-07-01 | 1982-01-05 | Unilever Limited | Detergent compositions |
US4375421A (en) * | 1981-10-19 | 1983-03-01 | Lever Brothers Company | Viscous compositions containing amido betaines and salts |
JPS6039719B2 (en) * | 1982-05-11 | 1985-09-07 | 花王株式会社 | liquid cleaning composition |
-
1985
- 1985-12-02 IN IN1013/DEL/85A patent/IN165674B/en unknown
- 1985-12-02 NZ NZ214410A patent/NZ214410A/en unknown
- 1985-12-03 ZA ZA859267A patent/ZA859267B/en unknown
- 1985-12-05 ZW ZW220/85A patent/ZW22085A1/en unknown
- 1985-12-06 MX MX856A patent/MX162411A/en unknown
- 1985-12-06 AU AU50844/85A patent/AU578333B2/en not_active Ceased
- 1985-12-10 FI FI854875A patent/FI79135C/en not_active IP Right Cessation
- 1985-12-11 IT IT48909/85A patent/IT1182083B/en active
- 1985-12-12 FR FR8518433A patent/FR2574813B1/en not_active Expired
- 1985-12-12 PT PT81670A patent/PT81670B/en not_active IP Right Cessation
- 1985-12-13 SE SE8505909A patent/SE466262B/en not_active IP Right Cessation
- 1985-12-14 DE DE19853544236 patent/DE3544236A1/en not_active Ceased
- 1985-12-16 PH PH33179A patent/PH24520A/en unknown
- 1985-12-16 TR TR50127/85A patent/TR23505A/en unknown
- 1985-12-17 KR KR1019850009487A patent/KR930003937B1/en not_active IP Right Cessation
- 1985-12-17 AR AR302608A patent/AR240336A1/en active
- 1985-12-17 BE BE0/216022A patent/BE903874A/en not_active IP Right Cessation
- 1985-12-17 CA CA000497898A patent/CA1255182A/en not_active Expired
- 1985-12-17 ZM ZM98/85A patent/ZM9885A1/en unknown
- 1985-12-17 BR BR8506327A patent/BR8506327A/en not_active IP Right Cessation
- 1985-12-17 LU LU86213A patent/LU86213A1/en unknown
- 1985-12-17 IE IE319185A patent/IE58699B1/en not_active IP Right Cessation
- 1985-12-17 GR GR853046A patent/GR853046B/el unknown
- 1985-12-17 NO NO855083A patent/NO165926C/en unknown
- 1985-12-18 EG EG810/85A patent/EG17366A/en active
- 1985-12-18 NL NL8503482A patent/NL8503482A/en not_active Application Discontinuation
- 1985-12-18 JP JP60285395A patent/JPS61145298A/en active Pending
- 1985-12-18 DK DK591785A patent/DK160771C/en not_active IP Right Cessation
- 1985-12-18 CH CH5421/85A patent/CH668078A5/en not_active IP Right Cessation
- 1985-12-18 AT AT0365685A patent/AT394378B/en not_active IP Right Cessation
- 1985-12-18 GB GB08531144A patent/GB2170816B/en not_active Expired
-
1991
- 1991-05-30 HK HK411/91A patent/HK41191A/en unknown
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Patent lapsed |