US3823094A - Two part liquid car wash system - Google Patents

Two part liquid car wash system Download PDF

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US3823094A
US3823094A US00296509A US29650972A US3823094A US 3823094 A US3823094 A US 3823094A US 00296509 A US00296509 A US 00296509A US 29650972 A US29650972 A US 29650972A US 3823094 A US3823094 A US 3823094A
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car wash
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A Lancz
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Colgate Palmolive Co
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/34Organic compounds containing sulfur
    • C11D3/3418Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/42Amino alcohols or amino ethers
    • C11D1/44Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines

Definitions

  • a liquid concentrate for automatic car wash machines designed to be stored in two parts, one of said parts containing K P O and nitrilotriacetic acid trisodium salt, these constituting 30-60 weight percent of said part and the other part containing an ethoxylated nonionic surfactant, a hydrotrope, a viscosity controlling agent and monoethanolamine as a pH stabilizer.
  • the two parts are mixed in a volume ratio from 1:2 to about 2:1 with a quantity of water to produce a stock solution.
  • the present invention relates to a liquid formulation suitable for washing automobiles and including as the primary active ingredients detergent and builder components present in an aqueous solution.
  • the new formulation is stored by the car washing facility in two parts, namely an aqueous detergent solution and an aqueous builder solution, that are mixed together prior to use with a quantity of water.
  • the individual detergent and builder solutions are formulated so that equal parts of each are mixed with a large quantity of water, to form a stock solution that is ultimately utilized to wash automobiles or the like.
  • a good built liquid car wash formulation should contain certain essential ingredients, i.e., a nonionic surfactant, inorganic builders, water softeners, solubilizers, and viscosity modifiers. It has not been possible to combine these various ingredients at optimum levels into a stable liquid formulation. Unfavorable cloud points and gelling have dogged past attempts at developing a commercially superior car wash concentrate.
  • the detergent concentrate is stored in two moieties which are mixed and diluted shortly before use.
  • One of the said moieties is a liquid solution containing tetrapotassium pyrophosphate and nitrilotriacetic acid sodium salt in a combined amount of 30-60 weight percent.
  • the other part contains an ethoxylated nonionic surfactant and a hydrotrope (sufficient in amount to solublize the ingredients of both parts when mixed with water to form a stock solution).
  • viscosity controlling agents and monoethanolamine the latter being present in order to stabilize the pH of this part.
  • Part I of the two part liquid car wash formulation contains two builders, the trisodium salt of nitrilotriacetic acid (triglycollamic acid) and tetrapotassium pyrophosphate. Both builders possess water softening properties.
  • NTANa nitrilotriacetic acid trisodium salt
  • K4P207 should comprise between 0 and 60 percent by weight. However, the total of these two ingredients should remain between 30 and 60 percent by weight the remainder being water. For commercial purposes, a small amount of dye will normally be added to such an aqueous solution.
  • Nonionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group and a hydrophilic group which is a reaction product of a solubilizing group such as carboxylate, hydroxyl,
  • amido or amino with an alkylene oxide, e.g., ethylene oxide or with the polyhydration product thereof, e.g., polyethylene glycol.
  • alkylene oxide e.g., ethylene oxide
  • polyhydration product thereof e.g., polyethylene glycol
  • nonionic surface active agents there may be noted the condensation products of alkyl phenols with ethylene oxide, e.g., the reaction product of isooctyl phenol with about 6 to 30 ethylene oxide units; condensation products of alkyl thiophenols with 10 to 15 ethylene oxide units; condensation products of higher fatty alcohols such as tridecyl alcohol with ethylene oxide; ethylene oxide addends of monoesters of hexahydric alcohols and inner ethers thereof such a sorbitan monolaurate, sorbitol monooleate and mannitant mono palmitate, and the condensation products of polypropylene glycol with ethylene oxide.
  • nonionics include the alkylolamine condensates of higher fatty acids such as lauric and myristic monoand di-ethanolamide; the higher alkyl amine oxides such as lauryl dirnethylamine oxide, lauryl bis (hydroxyethyl) amine oxide; higher alkyl monoand di-sulfoxides, phosphine oxides and the like.
  • the nonionic component of Part II is preferably a polyalkylene oxide ether of higher aliphatic alcohols.
  • Suitable fatty alcohols having a hydrophobic character, preferably 8 to 22 carbons, are lauryl, myristic, cetyl, stearyl and oleyl alcohols which may be condensed with an appropriate amount of ethylene oxide, such as at least about 3 and, preferably, about 6 to 12 moles.
  • Preferred in the practice of this invention is an cthoxylated (6.5 moles) (I -C fatty alcohol such as Neodol 23-65.
  • Another typical product usable in this invention is oleyl alcohol condensed with 6 moles of ethylene oxide.
  • the nonionic component should be at least 10 per-cent by weight of Part II and can vary up to nearly percent.
  • a water-soluble alkali metal sulfonated hydrotropic salt is effective in promoting the compatibility of the ingredients.
  • Suitable materials are the alkali metal or ammonium organic sulfonated salts having a lower alkyl group up to about 6 carbons, such as the sodium and potassium xylene, toluene, ethylbenzene and isopropylbenzene sulfonates. Any suitable isomeric mixture may be employed.
  • hydrotropes should be present under 10 percent by weight.
  • polyethoxylated tertiary aliphatic amines possessing one alkyl group ranging from (l -C in chain length and two polyoxyethylene groups are suitable. These, as commercial formulations are, for example, available under the trademark Ethomeen.
  • Such hydrotropes should be present in a concentration of less than 1 percent by weight.
  • organic solvents such as lower aliphatic monohydric alcohols such as ethanol, propanol and isopropanol, glycols, glycol ether and esters.
  • a mixture of isopropanol and ethylene glycol alkyl ethers such as ethylene glycol monoethyl ether and glycol monobutyl ether are preferred.
  • the solvent should be present in a concentration ranging from about 4 to about 20 percent and preferably from 8 to 12 percent by weight.
  • compositions of the present invention may include ethanolamine in amounts ranging from percent to about 1 percent.
  • the monoethanolamine may contain trace amounts of NaOH (0.004 percent by weight). It has been found that this inclusion prevents a large pH draft. For example, inclusion of this in a concentration of 0.1 percent by weight lowered the change in pH to 0.35 pH units in one week after preparation of Part II from a pH drop of 2.8 pH units in one week found in a similar formula without the monoethanolamine. Less than 1 percent by weight of monoethanolamine is sufficient. Less than 1 percent by weight of monoethanolamine is sufficient and as will be seen in the examples can be used satisfactorily in extremely small concentrations (e.g., 0.1 percent by weight).
  • the saline requirement with regard to monoethanolamine concentration is that such ingredient be present in amounts sufficient to stabilize the pH of the composition.
  • a suitable dye is commercially advantageous.
  • the invention does not preclude the use of other known ingredients which may be desirable in certain situations such as compatible perfumes and corrosion inhibitors.
  • Part I and Part II formulations are separately prepared and subsequently mixed with a predetermined amount of water to form a stock solution.
  • Parts I and II can be added to water in a ratio by volume of from about 1:2 to about 2:1, to form a stock solution, that contains up to 15 volume percent of the combined Parts I and II, preferably between 5 and 15 volume percent.
  • the stock solution is diluted further by the car wash operator by water for direct use on automotive surfaces.
  • liquid detergent and builder moieties are prepared in any suitable manner.
  • the components were added and mixed inthe order shown. No unusual procedural steps were required.
  • Ethomeen C/25 is derived from cocoamine and has the chemical structure:
  • Avai1ab1e under the mark Neodol 23-65. 1 Composed of Thymol Blue (Thymolsulphonp-hthalein) indicator 0.10 50% NaOH 0.02 Deionized water 99.88
  • Part I has a pH of 11. 8201, a fluorescent green color and a specific gravity of about 1.5 grams/cc. at 80 F.
  • Part II has a maximum pH of 9.8 (a very small'downward drift occurs even using monoeth-anolamine with a trace of 'NaOI-I), an amber color, a viscosity of less than 40 200 centipoises at 80 F., and a specific gravity of about 1.0 grams/cc. at 80 F.
  • a stock solution sufficient to wash at least 85 cars can be formed by mixing 3.5 gallons each of Parts I and II-with 43 gallons of water.
  • the resulting 14 volume percent stock solution has a pH of 10.8 and is a blue color (in contradistinction to Parts I and II which are green and amber, respectively). Seventy-five ounces of this stock solution mixed in twenty gallons of Water during the washing operation is adequate for cleaning one car.
  • Ethomeen 0/25 is preferred over sodium xylene sulfonate on the basis that it sol-ubilizes the concentrates in water more efiiciently (on a weight basis) and cheaply.
  • Thymol Blue is preferred. This indicator changes color in the same pH range as phenolphthalein. Its acid form is yellow and its alkaline form is blue. I As stated previously, monoethanolamine with just a trace of NaOl-I drastically reduces (almost a fold decrease in pH units) the loss in alkalinity of compositions not incorporating this. For this reason, a composition such as that of Example 11 is not desirable.
  • Method of formulating a stock solution suitable for washing automobiles comprising the steps of (a) separately preparing a builder solution and a detergent solution by mixing predetermined ingredients;
  • ingredients of said builder solution consisting essentially of from 0 to 60 per- 3 cent by weight K3 0; and from 0 to 40 percent by weight of the trisodium salt of nitrilotriacetic acid, the total quantity of these two materials being between about 30 and 60 percent by weight and the remainder water;
  • said predetermined ingredients of said detergent solution consisting essentially of 10 percent to percent by weight of an ethoxylated C -C fatty alcohol containing from 3 to 12 moles of ethylene oxide, from 0.1 to 10 percent by weight of at least one hydrotrope selected from the groups consisting essentially of alkali metal and ammonium sulfonates of xylene, toluene, ethylbenzene and isopropyl benzene and polyethoxylated tertiary aliphatic amines containing one C -C alkyl group and two polyoxyethylene groups having a total of 15 ethylene oxide units, 0 to 1 percent by weight of ethanolamine, and from about 4 to about 20 percent by weight of a water-miscible organic solvent selected from the group consisting of lower monohydrie alkanols, lower alkyl ethers of ethylene glycol, and mixtures thereof;

Abstract

A LIQUID CONCENTRATE FOR AUTOMATIC CAR WASH MACHINES DESIGNED TO BE STORED IN TWO PARTS, ONE OF SAID PARTS CONTAINING K4P2O7 AND NITRILOTRIACETIC ACID TRISODIUM SALT, THESE CONSISTUTING 30-60 WEIGHT ERCENT OF SAID PART AND THE OTHER PART CONTAINING AN ETHOXYLATED NONIONIC SURFACTANT, A HYDROTROPE, A VISCOSITY CONTROLING AGENT AND MONOETHANOLAMINE AS A PH STABILIZER. THE TWO PARTS ARE MIXED IN A VOLUME RATIO FROM 1:2 TO ABOUT 2:1 WITH A QUANTITY OF WATER TO PRODUCE A STOCK SOLUTION.

Description

United States Patent O M US. Cl. 252527 2 Claims ABSTRACT OF THE DISCLOSURE A liquid concentrate for automatic car wash machines designed to be stored in two parts, one of said parts containing K P O and nitrilotriacetic acid trisodium salt, these constituting 30-60 weight percent of said part and the other part containing an ethoxylated nonionic surfactant, a hydrotrope, a viscosity controlling agent and monoethanolamine as a pH stabilizer. The two parts are mixed in a volume ratio from 1:2 to about 2:1 with a quantity of water to produce a stock solution.
RELATED APPLICATIONS This application is a continuation-in-part of copending application Ser. No. 789,940 filed Jan. 8, 1969, now abandoned, entitled Two Part Car Wash System.
BACKGROUND OF THE INVENTION The present invention relates to a liquid formulation suitable for washing automobiles and including as the primary active ingredients detergent and builder components present in an aqueous solution. The new formulation is stored by the car washing facility in two parts, namely an aqueous detergent solution and an aqueous builder solution, that are mixed together prior to use with a quantity of water. Preferably the individual detergent and builder solutions are formulated so that equal parts of each are mixed with a large quantity of water, to form a stock solution that is ultimately utilized to wash automobiles or the like.
A good built liquid car wash formulation should contain certain essential ingredients, i.e., a nonionic surfactant, inorganic builders, water softeners, solubilizers, and viscosity modifiers. It has not been possible to combine these various ingredients at optimum levels into a stable liquid formulation. Unfavorable cloud points and gelling have dogged past attempts at developing a commercially superior car wash concentrate.
In efforts to overcome such disadvantages, resort has been had to a number of undesirable devices. Most common, of course, is to reduce the proportions of the essential ingredients of the liquid formulations, but this results in poorer performance unless proportionately larger amounts of the detergent are used in the washing operation (which results in higher cost to the consumer). Another device is to resort to expensive combinations of specially purified surfactants with unduly large proportions of solubilizers. These latter substances should be kept to a minimum owing to the fact that they increase the cost of the built liquid detergent without contributing appreciably to detergcncy.
BRIEF SUMMARY OF INVENTION It is an object of this invention to provide a built liquid detergent formulation and a method of making same which contains optimal concentrations of the foregoing ingredients. Furthermore, it is another object of this invention to provide a method of mixing and diluting storage components of this detergent in such a manner as to provide an automobile detergent capable of adequately cleaning automobiles at a low consumer cost.
3,823,094 Patented July 9, 1974 According to the invention the detergent concentrate is stored in two moieties which are mixed and diluted shortly before use. One of the said moieties is a liquid solution containing tetrapotassium pyrophosphate and nitrilotriacetic acid sodium salt in a combined amount of 30-60 weight percent. The other part contains an ethoxylated nonionic surfactant and a hydrotrope (sufficient in amount to solublize the ingredients of both parts when mixed with water to form a stock solution). Also present are viscosity controlling agents and monoethanolamine, the latter being present in order to stabilize the pH of this part.
DETAILED DESCRIPTION OF THE INVENTION Part I of the two part liquid car wash formulation contains two builders, the trisodium salt of nitrilotriacetic acid (triglycollamic acid) and tetrapotassium pyrophosphate. Both builders possess water softening properties. NTANa (nitrilotriacetic acid trisodium salt) should be present in Part I in a concentration of between 0 and 50 percent by weight and K4P207 should comprise between 0 and 60 percent by weight. However, the total of these two ingredients should remain between 30 and 60 percent by weight the remainder being water. For commercial purposes, a small amount of dye will normally be added to such an aqueous solution.
These ingredients are uniquely compatible with Part II of the car wash product in terms of proper buffering and the stability and detergency of a stock solution of the two parts.
Part II of the car wash formulation contains a nonionic detergent as its primary active ingredient. Nonionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group and a hydrophilic group which is a reaction product of a solubilizing group such as carboxylate, hydroxyl,
amido or amino with an alkylene oxide, e.g., ethylene oxide or with the polyhydration product thereof, e.g., polyethylene glycol.
As examples of such nonionic surface active agents there may be noted the condensation products of alkyl phenols with ethylene oxide, e.g., the reaction product of isooctyl phenol with about 6 to 30 ethylene oxide units; condensation products of alkyl thiophenols with 10 to 15 ethylene oxide units; condensation products of higher fatty alcohols such as tridecyl alcohol with ethylene oxide; ethylene oxide addends of monoesters of hexahydric alcohols and inner ethers thereof such a sorbitan monolaurate, sorbitol monooleate and mannitant mono palmitate, and the condensation products of polypropylene glycol with ethylene oxide.
Other nonionics include the alkylolamine condensates of higher fatty acids such as lauric and myristic monoand di-ethanolamide; the higher alkyl amine oxides such as lauryl dirnethylamine oxide, lauryl bis (hydroxyethyl) amine oxide; higher alkyl monoand di-sulfoxides, phosphine oxides and the like.
Pursuant to the invention, the nonionic component of Part II is preferably a polyalkylene oxide ether of higher aliphatic alcohols. Suitable fatty alcohols having a hydrophobic character, preferably 8 to 22 carbons, are lauryl, myristic, cetyl, stearyl and oleyl alcohols which may be condensed with an appropriate amount of ethylene oxide, such as at least about 3 and, preferably, about 6 to 12 moles. Preferred in the practice of this invention is an cthoxylated (6.5 moles) (I -C fatty alcohol such as Neodol 23-65. Another typical product usable in this invention is oleyl alcohol condensed with 6 moles of ethylene oxide. The nonionic component should be at least 10 per-cent by weight of Part II and can vary up to nearly percent.
solubilize Part I and Part II ingredients in the stock A solution. The formulation of this invention permits the use of very small amounts of the hydrotrope component (not more than about 10 percent in any case). In any event, the concentration of hydrotrope can be as little as about 0.1 percent by weight. A water-soluble alkali metal sulfonated hydrotropic salt is effective in promoting the compatibility of the ingredients. Suitable materials are the alkali metal or ammonium organic sulfonated salts having a lower alkyl group up to about 6 carbons, such as the sodium and potassium xylene, toluene, ethylbenzene and isopropylbenzene sulfonates. Any suitable isomeric mixture may be employed. Such hydrotropes should be present under 10 percent by weight. Alternatively, polyethoxylated tertiary aliphatic amines possessing one alkyl group ranging from (l -C in chain length and two polyoxyethylene groups are suitable. These, as commercial formulations are, for example, available under the trademark Ethomeen. Such hydrotropes should be present in a concentration of less than 1 percent by weight.
In order to insure fluidity of the organic concentrate (Part II), it is desirable to incorporate compatible organic solvents. Examples of such are lower aliphatic monohydric alcohols such as ethanol, propanol and isopropanol, glycols, glycol ether and esters. A mixture of isopropanol and ethylene glycol alkyl ethers such as ethylene glycol monoethyl ether and glycol monobutyl ether are preferred. In any event, the solvent should be present in a concentration ranging from about 4 to about 20 percent and preferably from 8 to 12 percent by weight.
The compositions of the present invention may include ethanolamine in amounts ranging from percent to about 1 percent. The monoethanolamine may contain trace amounts of NaOH (0.004 percent by weight). It has been found that this inclusion prevents a large pH draft. For example, inclusion of this in a concentration of 0.1 percent by weight lowered the change in pH to 0.35 pH units in one week after preparation of Part II from a pH drop of 2.8 pH units in one week found in a similar formula without the monoethanolamine. Less than 1 percent by weight of monoethanolamine is sufficient. Less than 1 percent by weight of monoethanolamine is sufficient and as will be seen in the examples can be used satisfactorily in extremely small concentrations (e.g., 0.1 percent by weight). The saline requirement with regard to monoethanolamine concentration is that such ingredient be present in amounts sufficient to stabilize the pH of the composition.
As in Part I, a suitable dye is commercially advantageous. The invention, as set forth above and in the examples, does not preclude the use of other known ingredients which may be desirable in certain situations such as compatible perfumes and corrosion inhibitors.
In accordance with the method of the invention, Part I and Part II formulations are separately prepared and subsequently mixed with a predetermined amount of water to form a stock solution. Parts I and II can be added to water in a ratio by volume of from about 1:2 to about 2:1, to form a stock solution, that contains up to 15 volume percent of the combined Parts I and II, preferably between 5 and 15 volume percent. The stock solution is diluted further by the car wash operator by water for direct use on automotive surfaces.
The liquid detergent and builder moieties are prepared in any suitable manner. In preparing the concentrates of the examples, the components were added and mixed inthe order shown. No unusual procedural steps were required.
The following examples are further illustrative of the nature of the present invention, and it will be understood that the invention is not limited thereto. All amounts indicated arejn approximate percent by weight.
4: EXAMPLE 1 Part I Ingredients: Percent by weight Deionized water 11.44 1% D-&C Green No. 8 dye 0.06 v 5 60% K P O solution 73.50
40% Nitrilotriacetic acid trisodium salt (NTA-Na solution 15.00
10 Part II Ingredients: Percent by Weight Deionized water 30.60 Ethylene glycol monoethyl ether 8.00 Isopropanol 2.00 Monoethanolamine 0.10 Polyoxyethylene (15) cocoamine". 0.30 =C -C fatty alcohol (PEO 6.5) c 55.00 0.1% Thymol Blue solution 4.00
Available under the mark Cellosolve. Available under the mark Ethomeen C/25. Ethomeen (3/25 is derived from cocoamine and has the chemical structure:
Avai1ab1e under the mark Neodol 23-65. 1 Composed of Thymol Blue (Thymolsulphonp-hthalein) indicator 0.10 50% NaOH 0.02 Deionized water 99.88
Part I has a pH of 11. 8201, a fluorescent green color and a specific gravity of about 1.5 grams/cc. at 80 F. Part II has a maximum pH of 9.8 (a very small'downward drift occurs even using monoeth-anolamine with a trace of 'NaOI-I), an amber color, a viscosity of less than 40 200 centipoises at 80 F., and a specific gravity of about 1.0 grams/cc. at 80 F.
Although particular dyes are included in this example, it should be understood that other dyes are useful. The dyes may be completely left out of such a formula and the same functional results are obtained.
A stock solution suficient to wash at least 85 cars can be formed by mixing 3.5 gallons each of Parts I and II-with 43 gallons of water. The resulting 14 volume percent stock solution has a pH of 10.8 and is a blue color (in contradistinction to Parts I and II which are green and amber, respectively). Seventy-five ounces of this stock solution mixed in twenty gallons of Water during the washing operation is adequate for cleaning one car.
Both parts are quite stable. No change occurs within on?) week (minimum) at temperatures of 30 F. and
EXAMPLES 2-10 These examples are formulations of Part I which are compatible, albeit in varying degrees, with the Part II of Example 1 or with those of Examples 11-17 herein- The formulation of Example 1 (44 percent K -P O and 6 percent NTA-Na is the preferred embodiment. HOW- ever, all these variations are compatible with the Part II 7 composition of the invention in terms of pH and stability.
. Clou fatty alcohol 5 EXAMPLES 11-11 These are Part II formulations which are compatible, albeit in varying degrees, with the Part I compositions of Examples 1 to 10.
Ingredient 11 12 13 14 15 16 17 EGME 5.00 8.00 .00 Iso roEanol 2. l. 50 2. 00 00 10.
D M 5.) 1.00 2.00 10.00 Ethanol 2. 00 1. 00 Monoethanolamlne 1. kg
0.1% Thymol Blue I 4. 00 3.00 3. 00 1% Cnlcodur Turquoise GT .00 Delonized water 29.33 32. 00 29.00 22. 00 57. 90 68.40 19. 90 Oleyl alcohol 11 50. 00
l Ethyl glycol monoethyl ether available under the name "Cellosolve". b Dlethylene glycol monobutyl other. Pol'yoxyethylene (l) cocoamlne. S um xylene sultonate. I C r-Cu fatty alcohol I Thymol Blue indicator, 0.1 percent by weight; 50% NaOH, 0.02 percent by weight; deionized water, 99.88.
B Condensed with 6 moles 0t ethylene oxide.
In Examples 11 to 17, Ethomeen 0/25 is preferred over sodium xylene sulfonate on the basis that it sol-ubilizes the concentrates in water more efiiciently (on a weight basis) and cheaply. Although not necessary to the invention, .004 percent by weight of Thymol Blue is preferred. This indicator changes color in the same pH range as phenolphthalein. Its acid form is yellow and its alkaline form is blue. I As stated previously, monoethanolamine with just a trace of NaOl-I drastically reduces (almost a fold decrease in pH units) the loss in alkalinity of compositions not incorporating this. For this reason, a composition such as that of Example 11 is not desirable.
Although the present invention has been described with reference to particular embodiments and examples, it will be apparent to those skilled in the art that variations and modifications can be substituted therefor without departing from the principles and true spirit of the invention.
I claim:
1. Method of formulating a stock solution suitable for washing automobiles comprising the steps of (a) separately preparing a builder solution and a detergent solution by mixing predetermined ingredients;
(b) said predetermined. ingredients of said builder solution consisting essentially of from 0 to 60 per- 3 cent by weight K3 0; and from 0 to 40 percent by weight of the trisodium salt of nitrilotriacetic acid, the total quantity of these two materials being between about 30 and 60 percent by weight and the remainder water;
(c) said predetermined ingredients of said detergent solution consisting essentially of 10 percent to percent by weight of an ethoxylated C -C fatty alcohol containing from 3 to 12 moles of ethylene oxide, from 0.1 to 10 percent by weight of at least one hydrotrope selected from the groups consisting essentially of alkali metal and ammonium sulfonates of xylene, toluene, ethylbenzene and isopropyl benzene and polyethoxylated tertiary aliphatic amines containing one C -C alkyl group and two polyoxyethylene groups having a total of 15 ethylene oxide units, 0 to 1 percent by weight of ethanolamine, and from about 4 to about 20 percent by weight of a water-miscible organic solvent selected from the group consisting of lower monohydrie alkanols, lower alkyl ethers of ethylene glycol, and mixtures thereof;
(d) storing said builder and detergent solutions separately before use; and
(e) mixing said builder solution and said detergent solution in a volume ratio of from about 1:2 to about 2:1 with a quantity of water to produce a stock solution containing from about 5 to about 15 volume percent of said combined detergent and builder solutions.
2. The method of claim 1 wherein about 3.5 parts by volume of said builder solution and about 3.5 parts by volume of said detergent solution are mixed with about 43 parts by volume of water to form said stock solution.
References Cited OTHER REFERENCES,"
Amino Acid Chelating Agents in Detergent Applications" by R. R. Pollard, Soap and Chemical Specialties, September 1966, pp. 58-62, and -135.
LEON D. ROSDOL, Primary Examiner D. L. ALBRECHT, Assistant Examiner US. Cl. X.R. 25290, 139, 153, 529, 540, 546, Dig. 1, 14
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3953359A (en) * 1974-04-23 1976-04-27 Pierce Chemical Company Determination of phosphorus
FR2474526A1 (en) * 1980-01-24 1981-07-31 Sandoz Sa NEW BIODEGRADABLE DETERGENT COMPOSITIONS
US4675124A (en) * 1985-04-20 1987-06-23 Henkel Kommanditgesellschaft Auf Aktien Granular detergent of improved detergency containing 2 ethoxylated alcohols, an ethoxylated amine and an anionic
US4695396A (en) * 1985-02-07 1987-09-22 Henkel Kommanditgesellschaft Auf Aktien Two-component alkaline cleaning compositions and methods of preparing and using same
US4731194A (en) * 1982-12-13 1988-03-15 Henkel Kommanditgesellschaft Auf Aktien Silica-containing alkaline dispersions and their use in cleaning solid surfaces
US4806263A (en) * 1986-01-02 1989-02-21 Ppg Industries, Inc. Fungicidal and algicidal detergent compositions
US5145608A (en) * 1986-02-06 1992-09-08 Ecolab Inc. Ethoxylated amines as solution promoters
US5932023A (en) * 1997-02-25 1999-08-03 Ward; Glen Douglas Method of washing a vehicle using a two-part washing composition
US20050286963A1 (en) * 2004-06-28 2005-12-29 Water Works I, Inc. Cleaning tool

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3953359A (en) * 1974-04-23 1976-04-27 Pierce Chemical Company Determination of phosphorus
FR2474526A1 (en) * 1980-01-24 1981-07-31 Sandoz Sa NEW BIODEGRADABLE DETERGENT COMPOSITIONS
US4731194A (en) * 1982-12-13 1988-03-15 Henkel Kommanditgesellschaft Auf Aktien Silica-containing alkaline dispersions and their use in cleaning solid surfaces
US4695396A (en) * 1985-02-07 1987-09-22 Henkel Kommanditgesellschaft Auf Aktien Two-component alkaline cleaning compositions and methods of preparing and using same
US4675124A (en) * 1985-04-20 1987-06-23 Henkel Kommanditgesellschaft Auf Aktien Granular detergent of improved detergency containing 2 ethoxylated alcohols, an ethoxylated amine and an anionic
US4806263A (en) * 1986-01-02 1989-02-21 Ppg Industries, Inc. Fungicidal and algicidal detergent compositions
US5145608A (en) * 1986-02-06 1992-09-08 Ecolab Inc. Ethoxylated amines as solution promoters
US5932023A (en) * 1997-02-25 1999-08-03 Ward; Glen Douglas Method of washing a vehicle using a two-part washing composition
US20050286963A1 (en) * 2004-06-28 2005-12-29 Water Works I, Inc. Cleaning tool

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