AU625056B2 - Safe acidic hard surface cleaner - Google Patents
Safe acidic hard surface cleaner Download PDFInfo
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- AU625056B2 AU625056B2 AU29874/89A AU2987489A AU625056B2 AU 625056 B2 AU625056 B2 AU 625056B2 AU 29874/89 A AU29874/89 A AU 29874/89A AU 2987489 A AU2987489 A AU 2987489A AU 625056 B2 AU625056 B2 AU 625056B2
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- Prior art keywords
- acid
- cleaner
- detergent
- carbon atoms
- aminoalkylenephosphonic
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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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0017—Multi-phase liquid compositions
- C11D17/0021—Aqueous microemulsions
-
- 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
-
- 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
- C11D3/36—Organic compounds containing phosphorus
- C11D3/364—Organic compounds containing phosphorus containing nitrogen
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- 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)
Description
r;i o COMMONWEALTH OF AUST L Patent Act 195j 5 6 CO M P L E T E S P E C IF I C A TIO N
(ORIGINAL)
Class Int. Class Application Number Lodged Complete Specification Lodged Accepted Published t I SPriority 10 February 1988 Related Art Name of Applicant COLGATE-PALMOLIVE COMPANY S300 Park Avenue, New York New York 10022 United States of America Address of Applicant Actual Inventor/s Address for Service Michel Thomas, Baudouin Valange Genevieve Blandiaux F.B. RICE CO., Patent Attorneys, 28A Montague Street, BALMAIN 2041.
Complete Specification for the invention entitled: SAFE ACIDIC HARD SURFACE CLEANER The following statement is a full description of this invention including the best method of performing it known to us/ fe.i i; :i r a
I
h i:l
-R
I:
L
-2 This invention relates to a cleaner for hard surfaces, such as bathtubs, sinks, tiles, porcelain and enamelware, which removes soap scum, lime scale and grease from such surfaces without harming them. More particularly, the invention relates to an acidic microemulsion that can be sprayed onto the surface to be cleaned, and wiped off without usual rinsing, and still leave the cleaned surface bright and shiny. The invention also relates to a method for using such compositions.
Hard surface cleaners, such as bathroom cleaners and scouring cleansers, have been known for many years.
Scouring cleansers normally include a soap or synthetic organic detergent or surface active agent, and an abrasive. Such products can scratch relatively soft surfaces and can eventually cause them to appear dull.
Also, they are often ineffective to remove lime scale (usually encrusted calcium and magnesium carbonates) in normal use. Because lime scale can be removed by chemical reactions with acidic media various acidic cleaners have S" 20 been produced, and have met with various degrees of success. In some instances such cleaners have been Il failures because the acid employed was too strong and damaged the surfaces being cleaned. At oter times, the acidic component of the cleaner reacted objectionably with other components of the product, adversely affecting the detergent or perfume, for example. Some cleaners required 4 rinsing afterward to avoid leaving objectionable deposits4 on the cleaned surfaces. As a result of research performed in efforts to overcome the mentioned 30 disadvantages there has recently been made an improved liquid cleaning composition in stable microemulsion form which is an effective cleaner to remove soap scum, lime scale and greasy soils from hard surfaces, such as bathroom surfaces, and which does not require rinsing after use. Such a product is described in 1 'j I1l I -3- Australian Patent Application No 25062/88 entitled STABLE MICROEMULsION CLEANING COMPOSITION, which application is hereby incorporated by reference.
In particular, Example 3 nf that application discloses an acidic, clear, oil-in-water microemulsion which is therein described as being successfully employed to clean shower wall tiles of lime scale and soap scum that had adhered to them. Such cleaning was effected by applying the cleaner to the walls, followed by wiping or minimal rinsing, after which the walls were allowed to dry to a good shine.
The described microemulsion cleaner of the patent application is effective in removing lime scale and soap scum from hard surfaces, and is easy to use, but it has 15 been found that its mixture of acidic agents (succinic, glutaric and adipic acids) could damage the surfaces of some hard fixtures, such as those of materials which are not acid resistant. One of such materials is an enamel that has been extensively employed in Europe as a coating 20 for bathtubs, herein referred to as European enamel. It has been described as zirconium white enamel or zirconium white powder enamel, and has the advantage of being resistant to detergents, which makes it suitable for use on tubs, sinks, shower tiles and bathroom enamelware.
25 However, such enamel is sensitive to acids and is severely damaged by use of the microemulsion acidic cleaner based on the three organic carboxylic acids previously mentioned. That problem has been solved by the present invention, in which additional acidic materials are incorporated in the cleaner with the organic acids, and rather than exacerbating the problem, they prevent harm to such European enamel surfaces by such organic acids.
Also, a mixture of such additional acids, phosphonic and phosphoric acids, surprisingly further improves the safety of the aqueous cleaner for use on such European enamel L a I ^,1 -4surfaces and decreases the cost of the cleaner. Thus, the present invention allows the cleaning by the invented emulsion of European enamel surfaces, as well as any other acid resistant surfaces of bathtubs and other bathroom surfaces. However, the product should not be used on various other materials that are especially susceptible to attack by acidic media, such as marble.
In accordance with the present invention an acidic aqueous cleaner for bathtubs and other hard surfaced items, which are acid resistant or are of zirconium white enamel, which cleaner is of a pH in the range of 1 to 4, and which removes lime scale, soap scum and greasy soil from surfaces of such items without damaging such surfaces, comprises: a detersive proportion of synthetic organic detergent, which is capable of removing greasy soil from such surfaces; a lime scale and soap scum removing proportion of dicarboxylic acid(s) having 2 to carbon atoms therein; an aminoalkylene-phosphonic acid in such proportion as to prevent damage to zirconium white 20 enamel surfaces of items to be cleaned by the dicarboxylic 94 acid(s) when the cleaner is employed to clean such surfaces; and an aqueous medium for the detergent, dicarboxylic acid(s) and aminoalkylenephosphonic acid.
In the present compositions the synthetic organic detergent may be any suitable anionic, nonionic, amphoteric, ampholytic, zwitterionic or cationic detergent or mixture thereof, but the anionic and nonionic detergents are preferred, as are mixtures thereof. Of the anionics the more preferred are water soluble salts of t *30 lipophilic sulfonic and sulfuric acids, the lipophilic moeities of which include long chain aliphatic groups, preferably lomg chain alkyls, of 8 to 20 carbon atoms, more preferably of 12 to 18 carbon atoms. Although several different types of solubilizing cations may be present in the detergents it will usually be preferred i
'I
5 that they be alkali metal, sodium or potassium or a mixture thereof, ammonium, or lower alkanolamine, of 2 or 3 carbon atoms per alkanol moiety. It is a desirable feature of the present invention that sodium may be the alkali metal employed, and the emulsions resulting will be stable and effective.
Much preferred salts of lipophilic sulfonic acids are paraffin sulfonates, wherein the paraffin group is of 12 to 18 carbon atoms, preferably 14 to 17 carbon atoms.
Other useful sulfonates are olefin sulfonates wherein the olefin starting material is of 12 to 18 carbon atoms, 12 to 15, and linear alkylbenzene sulfonates wherein the alkyl is of 12 to 18 carbon atoms, preferably of 12 to 16 carbon atoms, 12 or 13. All such sulfonates will preferably be employed as their sodium salts, but other salts are also operative.
Much preferred salts of lipophilic sulfuric acids are of higher alkyl ethoxylate sulfuric acids, which may also o 2 be designated as higher alkyl ethyl sulfuric acids. The 0""20 higher alkyls of such compounds are of the chain lengths Sogiven above for this class of anionic detergents, 10 to 18 .6 oY carbon atoms, and preferably are of 10 to 14 carbon atoms, o 12 or about 12 carbon atoms. Such compounds should include from 1 to 10 ethylene oxide groups per mole, preferably 3 to 7 ethylene oxide groups per mole, e.g., A preferred cation is sodium but the cations mentioned S* above for solubilizing functions may be employed in o suitable circumstances.
The nonionic detergents that are useful in this 30 invention may be any of the nonionic detergents known to the art (as may be the anionic detergents that satisfy the conditions set in this specification). Many such o 0 detergents are described in the text Surface Active Agents (Their Chemistry and Technology) by Schwartz and Perry, and in the various annual editions of John W. McCutcheon's t -6- Detergents and Emulsifiers. However, they will usually be condensation products of a lipophilic moiety, such as a higher alcohol or phenol, or a propylene glycol or propylene oxide polymer, with ethylene oxide or ethylene glycol. In some of the condensation products of ethylene oxide and higher fatty alcohol or alkyl substituted phenol (in which the alkyl on the phenol nucleus is usually of 7 to 12 carbon atoms, preferably some propylene oxide may be blended with the ethylene oxide so that the lower alkylene oxide moiety in the nonionic detergent is mixed, whereby the hydrophilic-lipophilic balance (HLB) may be controlled.
Much preferred nonionic detergents present in the invented emulsions will be condensation products of a fatty alcohol of 8 to 20 carbon atoms with from 3 to moles of ethylene oxide, preferably of a linear alcohol of 9 to 15 carbon atoms, such as 9-11 or 11-13 carbon atoms or averaging about 10 or 12 carbons, with 3 to 15 moles of 20 ethylene oxide, such as 3-7 or 5-9 moles of ethylene Se 20 oxide, about 5 or 7 moles thereof. In place of the higher fatty alcohol one may use an alkylphenol, such as one of 8 to 10 carbon atoms in a linear alkyl, e.g., aoo nonylphenol, and the phenol may be condensed with from 3 to 20 ethylene oxide groups, preferably 8 to Similarly functioning nonionic detergents that are polymers of mixed ethylene oxide and propylene oxide may be substituted, at least in part,; for the other nonionics. Among such are those sold under the trademark Plurafac, such as Plurafac RA-30 and Plurafac LF-400, o* 30 available from BASF. Preferred such nonionics contain 3 to 10 ehtoxies, more preferably about 7, and 2 to 7 Y propoxy groups, more preferably about 4, and such are condensed with a higher fatty alcohol of 12-16, more preferably 13-15 carbon atoms to make a mole of nonionic detergent.
14k 7 The various nonionic detergents, and the anionic detergents are often mixtures, which are within singular designations herein.
The active acidic component of the emulsions is a carboxylic acid which is strong enough to lower the pH of the emulsion to one in the range of one to four. Various such carboxylic acids can perform this function but those which have been found effectively to remove soap scum and lime scale from bathroom surfaces best, while still not destabilizing the emulsion, are polycarboxylic acids, and of these the dicarboxylic acids are preferred. Of the dicarboxylic acids group, which includes those of 2 to carbon atoms, from oxalic acid through sebacic acid, suberic, azelaic and sebacic acids are of lower solubilities and therefore are not as useful in the present emulsions as the other diabesic aliphatic fatty acids, all of which are preferably saturated and straight chained. Oxalic and malonic acids, although useful as 0. reducing agents too, may be too strong for delicate hard 20 surface cleanings. Preferred such dibasic acids are those of the middle portion of the 2 to 10 carbon atom acid range, succinic, glutaric, adipic and pimelic acids, 0 especially the first three thereof, which fortunately are available commercially, in mixture. The diacids, after being incorporated in the invented emulsion, may be partially neutralized to produce the desired pH in the emulsion, for greatest functional effectiveness, with safety.
Phosphoric acid is one of the additional acids that 30 helps to protect acid-sensitive surfaces being cleaned with the present emulsion cleaner. Being a tribasic acid, it too may be pctially neutralized to obtain an emulsion *bo pH in the desired range. For example, it may be partially I. neutralized to the biphosphate, NaH 2
PO
4 or
NH
4
H
2
PO
4 8 Phosphonic acid, the other of the two additional acids for protecting acid-sensitive surfaces from the dissolving action of the dicarboxylic acids of the present emulsions, apparently exists only theoretically, but its derivatives are stable and are useful in the practice of the present invention. Such are considered to be phosphonic acids, as that term is used in this specification. The phosphonic acids are of the structure
OH
Y P 0, wherein Y is any suitable
OH
substituent, but preferably Y is alkylamino or N-substituted alkylamino. For example, a preferred phosphonic acid component of the present emulsions is aminotris-)methylenephosphonic) acid, which is of the formula N(CH 2 PH20 3 Among other useful phosphonic acids are ethylenediamine tetra-(methylenephosphonic) acid, and hexamethylenediamine tetra-(methylenephosphonic) acid, and diethylenetriamine penta-(methylenephosphonic) acid. Such class of compounds may be described as aminoalkylenephosphonic acids containing in the ranges of 1 to 3 amino nitrogens, 3 or 4 lower alkylenephosphonic acid groups in which the lower alkylene is of 1 or 2 carbon atoms, and 0 to 2 alkylene groups of 2 to 6 carbon atoms each, which alkylene(s) is/are present and join amino nitrogens when a plurality of such amino nitrogens i is present in the aminoalkylenephosphonic acid. It has been found that such aminoalkylenephosphonic acids, which also may be partially neutralized at the desired pH of the microemulsion cleaner, are of desired stabilizing and protecting effect in the invented cleaner, especially when present with phosphoric acid, preventing harmful attacks .o on European enamel surfaces by the diacid(s) components of the cleaner. Usually the phosphorus acid salts, if present, will be mono-salts of each of the phosphoric 9 9and/or phosphonic acid groups present.
The water that is used in making the present micro-emulsions may be tap water but is preferably of low hardness, normally being less than 150 parts per million of hardness, as calcium carbonate. Still, useful cleaners can be made from tap waters that are higher in hardness, up to 300 as CaCO 3 Most preferably the water employed will be distilled or deionized water, in which the content of hardness ions is less than usually being nil. Employment of such deionized water allows for the manufacture of a product of consistently good qualities, independent of hardness variations in the aqueous medium.
Various other components may desirably be present in the invented cleaners, including preservatives, antioxidants or corrosion inhibitors, cosolvents, cosurfactants, multivalent metal ion, perfumes, colorants and terpenes (and terpineols), but various other adjuvants conventionally employed in liquid detergents and hard surface cleaners may also be present provided that they do not interfere with the cleaning and scum- and scaleremoval functions of the cleaner. Of the various adjuvants (which are so identified because they are not necessary for the production of an operative cleaner, although they may be very desirable components of the cleaner) the most important are considered to be the St perfumes, which, with terpenes, terpineols and hydrocarbons (which may be substituted for the perfumes or added to them) function as especially effective solvents S 30 for greasy soils on hard surfaces being cleaned, and form the dispersed phases of oil-in-water (o/w) microemulsions. Also of functional importance are the L ii 0co-surfactant and polyvalent metal ions, with the former helping to stabilize the microemulsion and the latter aiding in improving detergency, especially for more dilute l ;i 1 i I 0 cleaners, and when the polyvalent salts of the anionic detergent employed are more effective detergents against the greasy soil encountered in use.
The various perfumes that have been found to be useful in forming the dispersed phase of the o/w microemulsion cleaners may be those normally employed in cleaning products, and preferably are normally in liquid state. They include esters, ethers, aldehydes, alcohols and alkanes employed in perfumery but of most importance are the essential oils that are high in terpene content.
It appears that the terpenes (and terpineols) coact with the detersive components of microemulsions to improve detergency of the invented compositions, in addition to forming the stable dispersed phase of the microemulsions.
In the present invention it has been found that especially when a piney perfume is being employed, one can decrease the proportion of comparatively expensive such perfume and P" can compensate for it with alpha-terpineol, and in some instances with other terpenes. For example, for every 1% S, 20 of perfume one can substitute from 60 to 90% of it, e.g., S" about 80%, with alpha-terpineol, and obtain essentially 0° 0 the same piney scent, with good cleaning and microemulsion S'o stability. Similarly, terpenes and other terpene-like compounds and derivatives may be employed, but alpha-terpineol is considered to be the best.
The polyvalent metal ion present in the invented cleaners may be any suitable such ion, including magnesium ,o (usually preferred), aluminum, copper, nickel, iron or calcium, and the ion or mixture thereof may be added in 30 any suitable form, sometimes as an oxide or hydroxide, but usually as a water soluble salt. It appears that the polyvalent metal ion reacts with the anion of the anionic detergent (or replaces the detergent cation, or makes an equivalent solution in the emulsion), which improves detergency and generally improves other properties of the j' 11 product, too, If the polyvalent metal ion reacts with the detergent anion to form an insoluble product such polyvalent ion should be avoided. For example, calcium reacts with paraffin sulfonate anion to form an insoluble salt, so calcium ions, such as might be obtained from calcium chloride, will be omitted from any emulsion cleaners of this invention that contain paraffin sulfonate detergent. Similarly, those polyvalent ions or other components of the invented compositions that will react adversely with other components will also be omitted. As was mentioned previously, the polyvalent metal ion will preferably be magnesium, and such will be added to the other emulsion components as a water soluble salt. A preferred such salt is magnesium sulfate, usually employed as itE heptahydrate (Epsom salts), but other hydrates thereof or the anhydride may be used too. Generally, the sulfates of the polyvalent metals will be used because the sulfate anion thereof is also the anion of some of the anionic detergents and is found in some such detergents as 20 a byproduct of neutralization.
The cosurfactant component(s) of the microemulsion cleaners reduce the interfacial tension or surface tension S' between the lipophilic droplets and the continuous aqueous -3 medium to a value that is often close to 10 dynes/cm., which results in spontaneous disintegrations of the dispersed phase globules until they become so small as to be invisible to the human eye, forming a clear microemulsion. In such a microemulsion the surface area of the dispersed phase increases greatly and its solvent power and grease removing capability are also increased, so that the microemulsion is significantly more effective as a cleaner for removing greasy soils than when the dispersed phase globules are of ordinary emulsion size.
S Among the cosurfactants that are useful in the invented cleaners are: water soluble lower alkanols of 2 to 4
I?
I:
Par 12 faa, a Ir a r a S ar o S a, carbon atoms per molecule (sometimes preferably 3 or 4); polypropylene glycols of 2 to 18 propoxy units; monoalkyl lower glycol ethers of the formula RO(X)nH, wherein R is
C
1 -4 alkyl, X is CH 2 CH20, CH 2
CH
2 CH20 or
CH(CH
3 )CH20, and n is from 1 to 4; monoalkyl esters of the formula R10(X)nH wherein R 1 is C2_ 4 acyl and X and n are as immediately previously described; aryl substituted alkanols of 1 to 4 carbon atoms; propylene carbonate; aliphatic mono-, di- and tricarboxylc acids of 3 to 6 carbon atoms; mono-, di- and tri hydroxy substituted aliphatic mono-, di- and tricarboxylic acids of 3 to 6 carbon atoms; higher alkyl ether poly-lower alkoxy carboxylic acids; lower alkyl mono-, di- and triesters of phosphoric acid wherein the lower alkyl is of 1 to 4 carbon atoms; and mixtures thereof.
Representative of such cosurfactants are succinic, glutaric and adipic acids, diethylene glycol monobutyl ether, dipropylene glycol monobutyl ether and diethylene glycol monoisobutyl ether, which are considered to be the most effective.
From the foregoing discussion of useful cosurfactants in the present cleaners it is apparent that succinic, glutaric and adipic acids, and a mixture of such components, are useful for lowering the pH of the product so that it removes soap scum and lime scale easily from surfaces to be cleaned, and at the same time they function as cosurfactants, improving the appearance of the product and making it more effective for removing grease from such surfaces. Similar dual effects may be obtained by use of others of the named acidic materials that have cosurfactant activities in the described cleaners.
Although it is highly preferred that the present cleaning compositions be in the form of aqueous microemulsions it is within the invention to utilize less preferred emulsions (wherein the dispersed phase globules 1 13 are larger in sizes), but in such cases the cleaning power of the product will be less because there will not be as good contact of the cleaner with the surface being treated. Also, although mocroemulsions are highly preferred embodiments of the invention, other emulsions and other forms of the composition may be used, such as gels, pastes, solutions, foams, and "aerosols", which include aqueous media.
In the invented cleaners it is important that the proportions of the components are in certain ranges so that the product may be most effective in removing greasy soils, lime scale and soap scum, and other deposits from the hard surfaces subjected to treatment, and so as to protect such surfaces during such treatment. As was previously referred to, the detergent should be present in detersive proportion, sufficient to remove greasy and oily soils; the proportion(s) of carboxylic acid(s) should be sufficient to remove soap scum and lime scale; the phosphonic acid or phosphoric and phosphonic acids mixture 20 should be enough to prevent damage of acid sensitive 0* surfaces by the carboxylic acid(s); and the aqueous medium Sshould be a solvent and suspending medium for the required °components and for any adjuvants that may be present, too. Normally, such percentages of components will be 2 to 8% of synthetic anionic organic detergent(s), 1 to 6% of synthetic organic nonionic detergent(s), 2 to 64% of aliphatic carboxylic acids (preferably diacids), 0.05 to of phosphoric acid or mono-salt thereof, and 0.005 to 2% of phosphonic acid(s), aminoalkylene-phosphonic acid(s), or mono-phosphonic salt(s) thereof; and the balance water and adjuvant(s), if any are present. Of the carboxylic acids it is preferred that a mixture of succinic, glutaric and adipic acids be employed, and the o0oo0 ratio thereof will most preferably be in the range of 1-3:1-6:1-2, with 1:1:1 and about 2:5:1 ratios being most L i i -13a preferred. The ratios of phosphonic acid (preferably aminoalkylenephosphonic acid) to phosphoric acid to aliphatic carboxylic diacids (or carboxylic acids) are usually about 1:1-20 20-500, preferably being 1:2-10 10-200, and more preferably being about 1 4 1 7 170 and 1 3 25, in three representative formulas. However, one may have ranges as wide as 1: 1-2,000 10-4,000 and sometimes the preferred range of dicarboxylic acid to phosphonic acid is 5:1 to 250:1.
Similarly, a mixture of succinic, glutaric and adipic acids may be of ratio of 0.8-4 0.8 10 1, and the ratio of dicarboxylic acid to phosphoric acid may be 5:2 to 25:1.
o ai
CI
o tt e I 4
I
0 01 t h i L nn n II '1 I I I f 14 Usually there will be present in the cleaner, especially when paraffin sulfonate is the detergent, 0.05 to and preferably 0.1 to 0.3% of polyvalent ion, preferably magnesium or aluminum, and more preferably magnesium. Also, the percentage of perfume will normally be in the 0.2 to 2% range, preferably being in the 0.5 to range, of which perfume at least 0.1% is terpene or terpineol. The terpineol is alpha-terpineol and is preferably added to allow a reduction in the amount of perfume, with the total perfume (including the alpha-terpineol) being 50 to 90% of terpineol, preferably about 80% thereof.
For preferred formulas of the present cleaners, which are different in that one contains two anionic detergents S" 15 and the other only one, the latter will contain 3 to 5% of
S.
1 sodium paraffin sulfonate wherein the paraffin is C 14 17 2 to 4% of nonionic detergent which is a condensation product of a fatty alcohol of 9 to 15 carbon atoms with 3 to 15 moles of ethylene oxide per mole of higher fatty alcohol, 3 to 7% of a 1:1:1 or 2:5:1 mixture of succinic, glutaric and adipic acids, 0.1 to 0.3% of phosphoric acid, 0.03 to 0.1% of aminotris-(methylenephosphonic acid), 0.1 to 0.2% of magnesium ion, 0.5 to 2% of perfume, of which 50 to S 4 Z) I
FA
II
thereof is alpha-terpineol, 0 to 5% of adjuvants and 75 to of water. More preferably, such cleaner will comprise or consist essentially of about 4% of sodium paraffin
(C
14 17 sulfonate, about 3% of the nonionic detergent, about 5% of 2:5:1 mix of the dicarboxylic acids, about 0.2% of phosphoric acid, about 0.05% of aminotris-(methylene-phosphonic acid), about 1% of perfume, which includes about 0.8% of alpha-terpineol, about 0.7% of magnesium sulfate (anhydrous), about 3% of adjuvants and about 83% of water.
The other preferred formula comprises 0.5 to 2% of sodium paraffin sulfonate wherein the araffin is C 14 17 2 to 4% of sodium ethoxylated higher fatty alcohol sulfate wherein the higher fatty alcohol is of 10 to 14 carbon atoms and which contains 1 to 3 ethylene oxide groups per mole, 2 to 4% of nonionic detergent which is a condensation product of fatty alcohol of 9 to 15 carbon atoms with 3 to 15 moles of ethylene oxide per mole of fatty alcohol, 3 to 7% of a 1:1:1 mixture of succinic, glutaric and adipic acids, 0.1 to 0.3% of phosphoric acid, 0.01 to 0.05% of aminotris-(methylenephosphonic acid), 0.09 to 0.17% of magnesium ion, 0.5 to 2% of perfume, of which at least 10% is terpene(s) and/or terpineol, 0 to of adjuvant(s) and 75 to 90% of water. More preferably, such cleaner, with two anionic detergents, will comprise or consist essentially of about 1% of sodium paraffin
(C
14 1 7 sulfonate, about 3% of sodium ethoxylated higher fatty alcohol sulfate wherein the higher fatty alcohol is lauryl alcohol and the degree of ethoxylation is 2 moles of ethylene oxide per mole, about 3% of nonionic detergent which is a condensation product of a
C
9 linear alcohol and 5 moles of ethylene oxide, about 5% of a 1:1:1 mixture of succinic, glutaric and adipic acids, about 0.2% of phosphoric acid, about 0.03% of aminotris-(methylenephosphonic acid), about 0.7% of (I S16 magnesium sulfate (anhydrous), about 2% of adjuvants and about 84% of water.
The pH of the various preferred microemulsion cleaners is usually 1-4, preferabyl 1.5-3.5, e.g. 3. The water content of the microemulsions will usually be in the range of 75 to 90%, preferably 80 to 85%, and the adjuvant content will be from 0 to usually 1 to If the pH is not in the desired range it will usually be adjusted with either sodium hydroxide or suitable acid, e.g., sulfuric acid, solutions, but normally the pH will be raised, not lowered, and if it is to be lowered more of the dicarboxylic acid mixture can be used, instead.
The cleaners of the invention, in microemulsion form, are clear o/w emulsions and exhibit stability at room temperature and at elevated and reduced temperatures, from 100 to 50 C. They are readily pourable and exhibit a viscosity in the range of 2 to 150 or 200 centipoises, 5 to 40 cp., as may be desired, with the viscosity being controllable, in part, by addition to the formula of 20 a thickener, such as lower alkyl celluloses, methyl cellulose, hydroxypropyl methyl cellulose, or water 0 soluble resin, polyacrylamide, polyvinyl alcohol.
Any tendency of the product to foam objectionably can be counteracted by incorporating in the formula free fatty acid or soap, in minor proportion, as is known in the .°0o detergent art (at low pH the soap turns to acid).
The liquid cleaners can be manufactured by mere 4 04 mixing of the various components thereof, with orders of additions not being critical. However, it is desirable for the various water soluble components to be mixed together, the oil soluble components to be mixed together in a separate operation, and the two mixes to be admixed, with the oil soluble portion being added to the water soluble portion (in the water) with stirring or other agitation. In some instances such procedure may be varied L: i i l
L
17 to prevent any undesirable reactions between components.
For example, one would not add concentrated phosphoric acid directly to magnesium sulfate or to a dye, but such additions would be of aqueous solutions, preferably dilute, of the components.
The cleaner may desirably be packed in manually operated spray dispensing containers, which are usually and preferably made of synthetic organic polymeric plastic material, such as poly-ethylene, polypropylene or polyvinyl chloride (PVC). Such containers also preferably include nylon or other non-reactive plastic closure, spray nozzle, dip tube and associated dispenser parts, and the resulting packaged cleaner is ideally suited for use in "spray and wipe" applications. However, in some instances, as when lime scale and soap scum deposits are heavy, the cleaner may be left on until it has dissolved or loosened the deposits, and may then be wiped off, or may be rinsed off, or multiple applications may be made, followed by multiple removals, until the deposits are gone. For spray applications the viscosity of the microemulsion (or ordinary emulsion, of that is used instead) will desirably be increased so that the liquid adheres to the surface to be cleaned, which is especially important when such surface is vertical, to prevent immediate run-off of the cleaner and consequent loss of effectiveness. Sometimes, the product may be formulated as an "aerosol spray type", so that its foam discharged from the aerosol container will adhere to the surface to be cleaned. At other times the aqueous medium may be such as to result in a gel or paste, which is deposited on the surface by hand application, preferably with a sponge or L cloth, and is removed by a combination of rinsing and wiping, preferably with a sponge, after which it may be t left to dry to a shine, or may be dried with a cloth. Of course, when feasible, the cleaned surface may be rinsed 1- -I 18 to remove all traces of acid from it.
The following examples illustrate but do not limit the invention. All parts, proportions and percentages in the examples, the specification and claims are by weight and all temperatures are in 0 C. unless otherwise indicated.
EXAMPLE 1 Component (by weight) Sodium paraffin sulfonate (paraffin of
C
14 17 Sodium lauryl ether sulfate (2 moles of ethylene oxide [EtO] per mole)
C
9 11 linear alcohol ethoxylate nonionic detergent (5 moles of EtO per mole) Magnesium sulfate heptahydrate (Epson salts) Succinic Acid Glutaric Acid Adipic Acid Aminotris (methylenephosphonic acid) Phosphoric acid Perfume (contains about 40% terpenes) Dye aqueous solution of blue dye) Sodium hydroxide (50% aqueous solution; decrease water amount by amount of NaOH solution used) Water (deionized) 1.00 3.00 3.00 1.35 1.67 1.67 1.67 0.03 0.20 1.00 0.10 q.s.
85.31
I,
I I c r re c ((tTL( I L 100.00 The microemulsion cleaner is made by dissolving the detergents in the water, after which the rest of the water soluble materials are added to the detergent solution, with stirring, except for the perfume and the pH adjusting agent (sodium hydroxide solution). The pH is adjusted to ;i -19 and then the perfume is stirred into the aqueous solution, instantaneously generating the desired microemulsion, which is clear blue, and of a viscosity in the range of 2-20 cp. If the viscosity is lower or if it is considered desirable for it to be increased there may be incorporated in the formula about 0.1 to 1% of a suitable gum or resin, such as sodium carboxymethyl cellulose or hydroxypropylmethyl cellulose, or polyacrylamide or polyvinyl aclohol, or a suitable mixture thereof.
The acid cleaner is packed in polyethytlene squeeze bottles equipped with polypropylene spray nozzles, which are adjustable to closed, spray and stream positions. In use, the microemulsion is sprayed onto "bathtub ring" on a bathtub, which also includes lime scale, in addition to soap scum and greasy soil. The rate of application is about 5 ml. per 5 meters of ring (which is about 3 cm.
r. wide). After application and a wait of about two minutes A the ring is wiped off with a sponge and is sponged off 20 with water. It is found that the greasy soil, soap scum, and even the lime scale, have been removed effectively.
In those cases where the line scale is particularly thick or adherent a second application may be desirable, but that is not considered to be the norm.
The tub surface may be rinsed because it is so easy to rinse a bathtub (or a shower) but such rinsing is not necessary. Sometimes dry wiping will be sufficient but if it is desired to remove any acidic residue the surface may be sponged with water or wiped with a wet cloth but in such case it is not necessary to use more than ten times the weight of cleaner applied. In other words, the I. surface does not need to be thoroughly doused or rinsed 4 with water, and it still will be clean and shiny (providing that it was originally shiny). In other uses of the cleaner, it may be employed to clean shower tiles, L 1 1 20 bathroom floor tiles, kitchen tiles, sinks and enamelware, generally, without harming the surfaces thereof. It is recognized that many of such surfaces are acid-resistant but a commercial product must be capable of being used without harm on even less resistant surfaces, such as European white enamel (often on a cast iron or sheet steel base), which is sometimes referred to as zirconium white powder enamel. It is a feature of the cleaner described above (and other cleaners of this invention) that they clean hard surfaces effectively, but they do contain ionizable acids and therefore should not be applied to acid-sensitive surfaces. Nevertheless, it has been found that they do not harm European white enamel bathtubs, in this example, which are seriously affected by cleaning with preparations exactly like that of this example except for the omission from them of the phosphonic acid or the phosphonic-phosphoric acid mixture.
The major component of the formulation that protects the European enamels is the phosphonic acid, and in the 20 formula the amount of such acid has been reduced below the mnimum normally required at a pH of 3. Yet, although is the minimum normally, when the phosphoric acid is 1 present, which is ineffective in itself at such pH, it increases the effect of the phosphonic acid, allowing a reduction in the proportion of the more expensive phosphonic acid In variations of the described formula, all components are kept the same and in the same proportions except for water, and phosphonic and phosphoric acids. In Experiment la, 0.05% of aminotris-(methylene-phosphonic acid) is employed and the phosphoric acid is omitted; in Experiment ib, 0.5% of ethylene diamine tetra-(methylenephosphonic acid) is employed, with no phosphoric acid; in Experiment ic, 0.5% of hexamethylene diamine tetra-(methylene-phosphonic acid) is used, with no i -21phosphoric acid, in Experiment Id, 0.4% of diethylene triamine penta-(methylenephosphonic acid) is present, without phosphoric acid; and in Experiment le, 0.10% of diethylene triamine penta-(methylenephosphonic acid) is employed, with 0.60% of phosphoric acid. The cleaning powers of formulas Id and le are about equivalent, showing that the presence of the phosphoric acid, essentially inactive as a protector of surfaces against the effects of the carboxylic acids present in the formula, decreases the proportion of phosphonic acid to protect the surfaces to 1/4 of that previously necessary. Similar effects are obtainable when phosphoric acid is used in the lb and lc formulas in about the same proportions as in Example 1 and Example le. If excessive foaming is encountered in use of the cleaner one may add an anti-foaming agent such as a silicone or a coco fatty acid. Alternatively, coco-diethanolamide may be added to increase foaming.
I I t I I ii .4
I
s 22 EXAMPLE 2 Component Sodium paraffin sulfonate
(C
14 17 paraffin) Nonionic detergent (condensation product of one mole of fatty
C
9 11 alcohol and 5 moles EtO) Magnesium sulfate heptahydrate Mixed succinic, glutaric and adipic acids (1:1:1) Aminotris-(methylenephosphonic acid) Phosphoric acid Perfume Dye aqueous solution of blue dye) Sodium hydroxide (50% aqueous solution; decrease water amount by amount of NaOH solution used) Water, deionized (by weight) 4.00 3.00 1.50 5.00 0.03 0.20 1.00 0.05 q.s.
85.22 100.00 eii S St S I S I U I i It S~ U US U I 1. i 1 r "s
*A,
4 0 23 The compositions of this example are made in the same manner as those of Example 1 and are tested in the same way, too, with similar good results. The microemulsions are a clear lighter blue and the pH thereof is adjusted to 3.0. The cleaners easily remove soap scum and greasy soils from hard surfaces and loosen and facilitate removal of lime scale, too, with minimal rinsing or spongeing, as reported in Example 1. The presence of the aminotris-(methylenephosphonic acid) prevents harm to the acid sensitive surfaces by the carboxylic acids, and the presence of the phosphoric acid allows reduction in the proportion of aminotris-(methylenephosphonic acid) used.
For example, in Example 2a, without any phosphoric acid present, it takes 0.10% of the aminotris-(methylenephosphonic acid) to prevent harm to European enamel by the cleaning composition. Similarly, in Example lb, wherein the forriuila is the same except that the phosphonic and phosphoric acids are replaced by 0.20% of phosphopnic acid (diethylene traimine penta-(methylenephosphonic acid) and 0.6% of phosphoric acid, European enamel is unharmed, whereas to obtain the same desirable effect without the phosphoric acid present requires 0.50% of the phosphonic acid. Similar results are obtained when the 0.5% of the phosphonic acid is replaced by the same proportion of ethylene diamine tetra-(methylenephosphonic acid) or hexamethylene diamine tetra-(methylenephosphonic acid), with and without supplemental phosphoric acid.
Thus, from this example (and Example 1) it is seen Sthat phosphoric acid, which is essentially ineffective to protect acid-sensitive surfaces against actions of carboxylic acids in the present cleaners, improves the protective effects of phosphonic acids, and does so significantly for European bathtub enamel.
tc
I
I :Rj! wi.,.til~ ai: U.r: 24 EXAMPLE 3 Component Deionized water
C
14 17 paraffin sodium sulfonate active, Hostapur SAS) *Mixture of Glutaric, succinic and adipic acids (mf'd. by GAF Corp).
Nonionic detergent (Plurafac ethoxypropoxy higher fatty alcohol, mf'd. by BASF-Wyandotte) Epsom salts Aminotris-(methylenephosphonic acid) Phosphoric acid (85%) Perfume (pine scent type, containing terpenes) Alpha-terpineol (perfume substitute) Formalin (preservative) 2,6-Di-tert-butyl-para-cresol (antioxidant) CI Acid Blue 104 dye *57.5% glutaric acid, 27% succinic acid and 12% of adipic acid (by weight) 82.339 6.670 5.000 3.000 1.500 0.050 0.230 0.200 0.800 0.200 0.010 0.001 100.000 4 i 4 4$ i 4 I 4 4* 4 4.
i u 4 44 4 €4 ii 1 ii ii l i 44 44 4 44 4 m 25 The above formula is made in the manner previously described and is similarly tested and found satisfactorily to clean acid sensitive hard surfaced items, such as tubs and sinks of cast iron or sheet steel coated with European enamel, of greasy soils on them, and to facilitate removals of soap scums and lime scales from such surface.
When the phosphonic and phosphoric acids are omitted from the formula, or when only the phosphonic acid is omitted, the cleaner attacks such surfaces and dissolves them.
The presence of the phosphoric acid allows a reduction in the proportion of the phosphonic acid that is required to inhibit the cleaner so that it will not attack the European enamels, and that reduction is significant, especially for economic reasons, but also functionally.
The alpha-terpineol replaces some of the perfume and helps in the formation of the microemulsion, while not destroying the pleasant scent that the perfume imparts to the product, and such results are obtainable with other pine-type perfumes. The alpha-terpineol, like the torpene components of a pine-type perfume, facilitates Smicroemulsion formation, but the terpineol is even more active because it is essentially 100% of terpene type t compound, whereas the perfumes are usually less than of terpenes.
EXAMPLE 4 When variations are made in the formulas given above, by substituting different anionic and nonionic detergents, S of types described herein, by utilizing other polyvalent salts (or omitting them), by employing"other phosphonic Si 30 acids, with or without phosphoric acid, and by varying the proportions of components 10%, 20% and 30%, within the ranges given in the specification, ;useful microemulsion 'I cleaners are obtainable that will satisfactorily clean hard surfaces and remove soap scum and lime scale from them, without damaging them, even when they are of I I 26 European enamel. The products preferably contain phosphoric acid, which improves the protective action of the phosphonic acid component, but it is within the invention to omit the phosphoric acid, if that is considered to be desirable and feasible. The cleaners are preferably in microemulsion form but even if the microemulsion should "break" to an ordinary emulsion the product will be useful as an effective cleaner, so such emulsions are also within the invention. It may be preferred to dispense the cleaner from a spray bottle but it can be packaged in conventional bottleg, also. It may be made in paste or gel form so as to make it more adherent to surfaces to which it is applied, so that it will remain on them, working to attack the lime scale, rather than running down off the surface. Furthermore, while mixtures have been mentioned in this specification, even where they were not specifically referred to it should be considered that mention of a single component 2 includes reference to mixtures of such components in the invented cleaners.
This invention has been described wth respect to illustrations and embodiments thereof but it is not to be a limited to them because one of ordinary skill in the art will be able, with the benefit of applicants' teaching before him/her, to utilize substitutes and equivalents without departing from the invention.
I t S•t I 4
C.
Claims (12)
1. An acidic aqueous cleaner for bathtubs and other hard surfaced items, which are acid resistant or are of zirconium white enamel, which cleaner is of a pH in the range of 1 to 4, and which removes lime scale, soap scum and greasy soil from surfaces of such items without damaging such surfaces, which comprises: a detersive proportion of synthetic organic detergent, which is capable of removing greasy soil from such surfaces; a lime scale and soap scum removing proportion of dicarboxylic acid(s) having 2 to 10 carbon atoms therein; an aminoalkylenephosphonic acid in such proportion as to prevent damage to zirconium white enamel surfaces of items to be cleaned by the dicarboxylic acid(s) when the cleaner is employed to clean such surfaces; and an aqueous medium for the detergent, dicarboxylic acid(s) and aminoalkylenephosphonic acid.
2. An acidic aqueous cleaner according to claim 1 f, wherein the dicarboxylic acid(s) is/are aliphatic and of carbon atoms content in the range of 3 to 8, the aminoalkylenephosphonic acid contains 1 to 3 amino nitrogen(s), 3 or 4 lower alkylene phosphonic acid groups and 0 to 2 lower alkylene groups of 2 to 6 carbon atoms each, which alkylene(s) is/are present and connect(s) amino nitrogens when a plurality of such nitrogens is present in the aminoalkylenephosphonic acid.
3. An acidic aqueousimmin cleaner according to claim 2, which is in liquid emulsion form and in which the ratio Sof dicarboxylic acid to aminoalkylenephosphonic acid is in the range of 5:1 to 250:1.
4. An acidic aqueous emulsion cleaner according to claim 3 wherein the synthetic organic detergent is a mixture of i ,anionic and nonionic detergents, wherein the anionic i detergent(s) is/are water soluble salt(s) of lipophilic organic sulfonic acid(s) and/or water soluble salt(s) of 28 lipophilic organic sulfuric acid(s), wherein the nonionic detergent is a condensation product of a lipophilic alcohol or phenol with lower alkylene oxide, and wherein the aminoalkylenephosphonic acid is selected from the group consisting of aminotris-(methylenephosphonic acid), ethylenediamine tetra-(methylenephosphonic acid), hexamethylene diamine tetra-(methylenephosphonic acid), and diethylene-triamine penta-(methylenephosphonic acid), and mixtures thereof. An acidic aqueous emulsion liquid cleaner in which there is also present phosphoric acid, which improves the action of the aminoalkylenephosphonic acid in protecting zirconium white enamel surfaces of items being cleaned against the action of the dicarboxylic acid(s), and in which the proportion of phosphoric acid is in the range of 2:1 to 10:1 with respect to the aminoalkylenephosphonic acid and the ratio of dicarboxylic acid to phosphoric acid is in the range of 5:2 to 25:1.
6. An acidic liquid emulsion cleaner according to claim which comprises 2 to 8% of synthetic organic anionic detergent(s), 1 to 6% of synthetic organic nonionic detergent(s), 2 to 10% of aliphatic carboxylic diacid(s), 0.05 to 5% of phosphoric acid and O.Oo-to Z.0% of aminoalkylenephosphonic acid(s).
7. An acidic liquid emulsion cleaner according to claim 6 wherein the synthetic organic anionic detergent is I r selected from the group consisting of water soluble higher i' paraffin sulfonate and water soluble ethoxylated higher fatty alcohol sulfate having 1 to 10 ethylene oxide groups per mole, and mixtures thereof, the nonionic detergent is a condensation product of a fatty alcohol of 9 to carbon atoms with from 3 to 15 moles of lower alkylene ,I oxide per mole of higher fatty alcohol, the mixture of succinic, glutaric and adipic acids is one of proportions of 0.8 4 0.8 10 1, the aminoalkylenephosphonic 1 I 1 1 1 U n9r -29 acid is amino-tris-(methylenephosphonic acid) and there are present in the cleaner 0.05 to 0.5% of magnesium and/or aluminium ion and 0.2 to 2% of perfume material, containing at least 0.1% of terpene and/or terpineol, which cleaner is in microemulsion form.
8. An acidic liquid microemulsion cleaner according to claim 7 which is of a pH in the range of 2.5 to 3.5 and which comprises 3 to 5% of sodium paraffin sulfonate wherein the paraffin is C 14 17 2 to 4% of nonionic detergent which is a condensation product of a fatty alcohol of 9 to 15 carbon atoms with 3 to 15 moles of lower alkylene oxide per mole of higher fatty alcohol, 3 to 7% of the mixture of succinic, glutaric and adipic acids, 0.1 to 0.3% of phosphoric acid, 0.03 to 0.1% of aminotris-(methylenephosphonic acid), 0.1 to 0.2% of magnesium ion, 0.5 to 2% of perfume, of which 50 to thereof is alpha-terpineol, 0 to 5% of adjuvants and 75 to 90% of water.
9. An acidic liquid microemulsion cleaner according to t claim 8 which comprises about 4% of sodium paraffin sulfonate, about 3% of nonionic detergent, about 5% of S-aeof a 2:5:1 mixture of succinic, glutaric and adipic acids, about 0.2% of phosphoric acid, about 0.05% of aminotris-(methylenephosphoni acid), about 1% of perfume, about 0.7% of magnesium sulfate, anhyd., about 1% of adjuvants and about 81% of water. An acidic liquid microemulsion cleaner according to Sclaim 7 which comprises 0.5 to 2% of sodium paraffin sulfonate wherein the paraffin is C 14 17 2 to 4% of sodium ethoxylated higher fatty alcohol sulfate wherein the higher fatty alcohol is of 10 to 14 carbon atoms and which contains from 1 to 3 ethylene oxide groups per mole, 2 to 4% of nonionic detergent which is a condensation product of fatty alcohol of 9 to 15 carbon atoms with 3 to moles of ethylene oxide per mole of higher fatty ;E 0piLAS ©i -4 I 4 i 30 alcohol, 3 to 7% of an about 1:1:1 mixture of succinic, glutaric and adipic acids, 0.1 to 0.3% of phosphoric acid, 0.01 to 0.05% of aminotris-(methylenephosphonic acid), 0.09 to 0.17% of magnesium ion, 0.5 to 2% of perfume, of which at least 10% is terpene(s) and/or terpineol, 0 to of adjuvant(s) and 75 to 90% of water.
11. An acidic liquid microemulsion cleaner according to claim 10 which comprises about 1% of sodium paraffin sulfonate, about 3% of sodium ethoxylated higher fatty alcohol sulfate, about 3% of nonionic detergent, about of 1:1:1 mixture of succinic, glutaric and adipic acids, about 0.2% of phosphoric acid, about 0.03% of aminotris-(methylene phosphonic acid), about 0.7% of magnesium sulfate, about 1% of perfume, about 1% of adjuvants and about 85% of water.
12. A process for removing any one or more of lime scale, soap scum, and greasy soil from bathtubs or other hard surfaced items, which are acid resistant or are of zirconium white enamel, which comprises applying to such a surface a composition in accordance with claim 1, and removing such composition and the lime scale and/or soap scum and/or greasy soil from such surface.
13. A process for removing any one or more of lime scale, soap scum, and greasy soil from bathtubs or other hard surfaced items, which are acid resistant or are of zirconium white enamel, which comprises applying to such surface a composition in accordance with claim 7, and removing such composition and the lime scale and/or soap scum and/or greasy soil from such surface.
44..' '4 t V 4 I 'f 4 r 4, V( 4 t( 4 Vi I. i- r DATED this 10th day of February 1989 4 '4 I~ 0 COLGATE-PALMOLIVE COMPANY Patent Attorneys for the Applicant: F.B. RICE CO. A
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15483788A | 1988-02-10 | 1988-02-10 | |
US154837 | 1988-02-10 |
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Publication Number | Publication Date |
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AU2987489A AU2987489A (en) | 1989-08-10 |
AU625056B2 true AU625056B2 (en) | 1992-07-02 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU29874/89A Ceased AU625056B2 (en) | 1988-02-10 | 1989-02-10 | Safe acidic hard surface cleaner |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0336878B1 (en) |
AR (1) | AR242256A1 (en) |
AT (1) | ATE122383T1 (en) |
AU (1) | AU625056B2 (en) |
BR (1) | BR8900594A (en) |
CA (1) | CA1332338C (en) |
DE (1) | DE68922522T2 (en) |
DK (1) | DK175385B1 (en) |
MX (1) | MX170213B (en) |
NO (1) | NO174430C (en) |
PT (1) | PT89679B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU668201B2 (en) * | 1992-09-24 | 1996-04-26 | Colgate-Palmolive Company, The | Thickened acid microemulsion composition |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5294364A (en) * | 1988-02-10 | 1994-03-15 | Colgate Palmolive | Safe acidic hard surface cleaner |
US5192460A (en) * | 1988-02-10 | 1993-03-09 | Colgate-Palmolive Company | Safe acidic hard surface cleaner |
US5279758A (en) * | 1991-10-22 | 1994-01-18 | The Clorox Company | Thickened aqueous cleaning compositions |
AU685758B2 (en) † | 1992-10-16 | 1998-01-29 | Unilever Plc | Improvements in general purpose cleaning compositions |
TR27813A (en) * | 1993-09-23 | 1995-08-29 | Colgate Palmolive Co | Stained acid microemulsion composition. |
CA2177063A1 (en) * | 1993-11-22 | 1995-06-01 | Anne-Marie Misselyn | Liquid cleaning compositions |
US5415813A (en) * | 1993-11-22 | 1995-05-16 | Colgate-Palmolive Company | Liquid hard surface cleaning composition with grease release agent |
AU1608695A (en) * | 1994-02-02 | 1995-08-21 | Colgate-Palmolive Company, The | Liquid cleaning compositions |
US5409630A (en) * | 1994-02-03 | 1995-04-25 | Colgate Palmolive Co. | Thickened stable acidic microemulsion cleaning composition |
ES2151538T3 (en) * | 1994-02-03 | 2001-01-01 | Procter & Gamble | ACID CLEANING COMPOSITIONS. |
WO1996003491A1 (en) * | 1994-07-21 | 1996-02-08 | Colgate-Palmolive Company | Liquid cleaning compositions |
AR006129A1 (en) * | 1996-03-06 | 1999-08-11 | Colgate Palmolive Co | A ACIDIC LIQUID CRYSTAL DETERGENT COMPOSITION AND A PROCESS TO REMOVE SOAP SLAG, LIME CRUSH AND FATTY DIRT SURFACES WITH SUCH COMPOSITION. |
US5707952A (en) * | 1996-04-24 | 1998-01-13 | Colgate-Palmolive Company | Thickened acid composition |
US7605114B2 (en) | 2005-05-03 | 2009-10-20 | Claudia Rushlow | Multi-purpose cleaner comprising blue iron powder |
WO2024031507A1 (en) * | 2022-08-11 | 2024-02-15 | Ecolab Usa Inc. | Detergent compositions with enhanced anti-scaling efficacy |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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US4501680A (en) * | 1983-11-09 | 1985-02-26 | Colgate-Palmolive Company | Acidic liquid detergent composition for cleaning ceramic tiles without eroding grout |
US4502986A (en) * | 1980-05-10 | 1985-03-05 | The Procter & Gamble Company | Stain removal method using granular detergent composition comprising magnesium salt |
AU5892590A (en) * | 1989-07-31 | 1991-01-31 | Colgate-Palmolive Company, The | Safe acidic hard surface cleaner |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1529466A (en) * | 1966-07-01 | 1968-06-14 | Monsanto Co | Washing compositions comprising a synthetic detergent and cycloalkanepolycarboxylic acids |
IT951279B (en) * | 1971-07-01 | 1973-06-30 | Benckiser Gmbh Joh A | PROCESS TO PREVENT THE FORMATION OF DEPOSITS THAT PRODUCE CROSSING IN AQUEOUS SYSTEMS |
ZA826902B (en) * | 1981-10-01 | 1984-04-25 | Colgate Palmolive Co | Safe liquid toilet bowl cleaner |
-
1989
- 1989-02-07 EP EP89730026A patent/EP0336878B1/en not_active Expired - Lifetime
- 1989-02-07 DE DE68922522T patent/DE68922522T2/en not_active Expired - Lifetime
- 1989-02-07 AT AT89730026T patent/ATE122383T1/en not_active IP Right Cessation
- 1989-02-09 CA CA000590542A patent/CA1332338C/en not_active Expired - Fee Related
- 1989-02-09 NO NO890559A patent/NO174430C/en unknown
- 1989-02-09 MX MX014866A patent/MX170213B/en unknown
- 1989-02-10 AU AU29874/89A patent/AU625056B2/en not_active Ceased
- 1989-02-10 AR AR89313196A patent/AR242256A1/en active
- 1989-02-10 PT PT89679A patent/PT89679B/en active IP Right Grant
- 1989-02-10 BR BR898900594A patent/BR8900594A/en not_active Application Discontinuation
- 1989-02-10 DK DK198900652A patent/DK175385B1/en not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4502986A (en) * | 1980-05-10 | 1985-03-05 | The Procter & Gamble Company | Stain removal method using granular detergent composition comprising magnesium salt |
US4501680A (en) * | 1983-11-09 | 1985-02-26 | Colgate-Palmolive Company | Acidic liquid detergent composition for cleaning ceramic tiles without eroding grout |
AU5892590A (en) * | 1989-07-31 | 1991-01-31 | Colgate-Palmolive Company, The | Safe acidic hard surface cleaner |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU668201B2 (en) * | 1992-09-24 | 1996-04-26 | Colgate-Palmolive Company, The | Thickened acid microemulsion composition |
Also Published As
Publication number | Publication date |
---|---|
AR242256A1 (en) | 1993-03-31 |
DE68922522D1 (en) | 1995-06-14 |
DE68922522T2 (en) | 1995-09-14 |
MX170213B (en) | 1993-08-11 |
ATE122383T1 (en) | 1995-05-15 |
DK65289A (en) | 1989-08-11 |
NO890559L (en) | 1989-08-11 |
NO174430B (en) | 1994-01-24 |
NO890559D0 (en) | 1989-02-09 |
NO174430C (en) | 1994-05-04 |
PT89679A (en) | 1989-10-04 |
BR8900594A (en) | 1989-10-10 |
EP0336878B1 (en) | 1995-05-10 |
EP0336878A3 (en) | 1990-09-19 |
EP0336878A2 (en) | 1989-10-11 |
DK65289D0 (en) | 1989-02-10 |
AU2987489A (en) | 1989-08-10 |
PT89679B (en) | 1994-04-29 |
DK175385B1 (en) | 2004-09-20 |
CA1332338C (en) | 1994-10-11 |
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