CA2287233A1 - Abrasive cleaning composition - Google Patents
Abrasive cleaning composition Download PDFInfo
- Publication number
- CA2287233A1 CA2287233A1 CA002287233A CA2287233A CA2287233A1 CA 2287233 A1 CA2287233 A1 CA 2287233A1 CA 002287233 A CA002287233 A CA 002287233A CA 2287233 A CA2287233 A CA 2287233A CA 2287233 A1 CA2287233 A1 CA 2287233A1
- Authority
- CA
- Canada
- Prior art keywords
- abrasive
- composition according
- mixtures
- solvent
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- 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
- C11D17/0013—Liquid compositions with insoluble particles in suspension
-
- 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
- C11D3/18—Hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
The invention provides a liquid abrasive cleaning composition of pH 7-13 which comprises: a) 0.1-20 wt.% of one or more surfactants forming a suspending system, b) 2-80 wt.% one or more suspended abrasives, c) 0.5-10 wt.% of a C2-C6 alkanolamine, and, d) 0.25-10 wt.% of a hydrocarbon co-solvent. The alkanolamine acts both as a base and a solvent which improves cleaning and so allows the level of suspended abrasive to be reduced so as to reduce the possibility of damage to surfaces and improve rinsing performance. It is believed that the presence of the hydrocarbon co-solvent is required to maintain the stability of the compositions at extremes of temperature.
Description
ABRASIVE CLEANING COMPOSITION
Technical Field The invention relates to pourable, homogenous, abrasive, aqueous liquid detergent compositions containing a particulate abrasive which are suited to the cleaning of hard surfaces.
Background to the Invention Hard surface cleaners containing abrasive particles are well known. Typical compositions comprise one or more surfactants in solution and a plurality of abrasive particles dispersed therein. Typical abrasive materials include minerals such as calcite or dolomite and other materials of relatively high density. In this art it is generally considered necessary to ensure that the abrasive particles remain in suspension in the composition in order that the composition need not be vigorously shaken before use and that sedimentation, or even cementing of precipitated particles, is prevented.
In one sub-class of compositions, one or more surfactant components act as a suspending agent, usually in combination with a dissolved electrolyte. The presence of the electrolyte causes the surfactant components) to thicken by the establishment of a lamellar phase. These compositions are generally formulated at a pH above 9.0 especially where calcite is used as the abrasive.
Technical Field The invention relates to pourable, homogenous, abrasive, aqueous liquid detergent compositions containing a particulate abrasive which are suited to the cleaning of hard surfaces.
Background to the Invention Hard surface cleaners containing abrasive particles are well known. Typical compositions comprise one or more surfactants in solution and a plurality of abrasive particles dispersed therein. Typical abrasive materials include minerals such as calcite or dolomite and other materials of relatively high density. In this art it is generally considered necessary to ensure that the abrasive particles remain in suspension in the composition in order that the composition need not be vigorously shaken before use and that sedimentation, or even cementing of precipitated particles, is prevented.
In one sub-class of compositions, one or more surfactant components act as a suspending agent, usually in combination with a dissolved electrolyte. The presence of the electrolyte causes the surfactant components) to thicken by the establishment of a lamellar phase. These compositions are generally formulated at a pH above 9.0 especially where calcite is used as the abrasive.
Surfactants employed as suspending agents in liquid abrasive cleaners have included, alkyl benzene sulphonates, alcohol sulphates, alcohol ethoxylates, alkyl amido ethoxylates, fatty acid soaps and secondary alkyl sulphonates. Combinations of these surfactants, together with electrolytes are used to form a suspending system as is well known in the art.
The fine structure of these suspending systems generally consists of spherical structures ranging from 0.05 to about 10 microns in diameter. These structures are believed to comprise concentric shells of alternating bilayers of surfactant molecules spaced apart by thin water layers. The suspending system is not the only structure which surfactants can form in the presence of water. The above-mentioned surfactants can also form micellar structures which are viscous but are not capable of suspending particles. In addition, compositions of surfactant and water may separate into two or more mixed phases with different physical properties. Exactly which structure is adopted by a particular surfactant mix is strongly influenced by the ionic strength of electrolyte in the composition and some surfactant systems can be exceptionally sensitive to changes in ionic strength of the electrolyte.
It is also known to use mixed suspending systems in which polymers are present. It is believed that in such compositions a part of the suspending activity of the products arises due to the presence of the polymers.
It is essential, in any commercially practical liquid abrasive cleaner which employs surfactants as the suspending system, that the suspending system is stable over the full range of temperatures encountered in use and sufficiently suspending to C3779 (C) maintain the abrasive particles in suspension for the shelf life of the product. Where the ionic strength of the composition changes with temperature, it is difficult to predict whether a given additive will disturb the suspending system in such a way that it ceases to suspend particles in some portion of the range of temperatures to which the product will be exposed. WO 94/05757 (Unilever) relates to stable liquid abrasive cleaners containing mixtures of primary alcohol sulphate and alkoxylated nonionic surfactant in a specific ratio range, which compositions also contain 1-20% of a dissolved electrolyte.
A further problem with liquid abrasive cleaners is their tendency to leave residues which are difficult to rinse away.
This is a particular problem with compositions which contain insoluble abrasives. There is therefore a need to improve the performance of abrasive compositions in such as manner that the overall level of abrasive can be reduced so as to improve rinsing performance and reduce the possibility of surface damage by the abrasive.
Solvents are well known components of non-abrasive cleaning compositions. Typical solvents used in cleaning compositions include, alcohols (such as ethanol), ethers (such as Butyl Cellosolve [TM]), paraffins (such as Isopar L [TM]), esters and terpenes (such as d-limonene). Another known class of solvents are the alkanolamines. EP503219A (P&G) relates to a cleaning composition containing 0.1 - 10~ of an alkanolamine.
From EP-A-0269178 (P&G) it is known to use hydrocarbon solvents in liquid abrasive cleaners, These solvents are optionally combined with polar solvents such as low water pN;tvDED SHEEj C3779 (C) 3a ' soluble alcohols and diols and highly water soluble diethylene glycol ether type solvents.
We have determined that it is difficult to include an alkanolamine solvent at significant levels in a liquid abrasive cleaner. It is believed that alkanolamines have both electrolyte and solvent properties and can influence the structure of the suspending phase. Consequently, as the temperature of the composition changes, on storage or during transportation, the level of effective electrolyte in the composition will also change and this can result in the p"'v~t~DED S~EE~
The fine structure of these suspending systems generally consists of spherical structures ranging from 0.05 to about 10 microns in diameter. These structures are believed to comprise concentric shells of alternating bilayers of surfactant molecules spaced apart by thin water layers. The suspending system is not the only structure which surfactants can form in the presence of water. The above-mentioned surfactants can also form micellar structures which are viscous but are not capable of suspending particles. In addition, compositions of surfactant and water may separate into two or more mixed phases with different physical properties. Exactly which structure is adopted by a particular surfactant mix is strongly influenced by the ionic strength of electrolyte in the composition and some surfactant systems can be exceptionally sensitive to changes in ionic strength of the electrolyte.
It is also known to use mixed suspending systems in which polymers are present. It is believed that in such compositions a part of the suspending activity of the products arises due to the presence of the polymers.
It is essential, in any commercially practical liquid abrasive cleaner which employs surfactants as the suspending system, that the suspending system is stable over the full range of temperatures encountered in use and sufficiently suspending to C3779 (C) maintain the abrasive particles in suspension for the shelf life of the product. Where the ionic strength of the composition changes with temperature, it is difficult to predict whether a given additive will disturb the suspending system in such a way that it ceases to suspend particles in some portion of the range of temperatures to which the product will be exposed. WO 94/05757 (Unilever) relates to stable liquid abrasive cleaners containing mixtures of primary alcohol sulphate and alkoxylated nonionic surfactant in a specific ratio range, which compositions also contain 1-20% of a dissolved electrolyte.
A further problem with liquid abrasive cleaners is their tendency to leave residues which are difficult to rinse away.
This is a particular problem with compositions which contain insoluble abrasives. There is therefore a need to improve the performance of abrasive compositions in such as manner that the overall level of abrasive can be reduced so as to improve rinsing performance and reduce the possibility of surface damage by the abrasive.
Solvents are well known components of non-abrasive cleaning compositions. Typical solvents used in cleaning compositions include, alcohols (such as ethanol), ethers (such as Butyl Cellosolve [TM]), paraffins (such as Isopar L [TM]), esters and terpenes (such as d-limonene). Another known class of solvents are the alkanolamines. EP503219A (P&G) relates to a cleaning composition containing 0.1 - 10~ of an alkanolamine.
From EP-A-0269178 (P&G) it is known to use hydrocarbon solvents in liquid abrasive cleaners, These solvents are optionally combined with polar solvents such as low water pN;tvDED SHEEj C3779 (C) 3a ' soluble alcohols and diols and highly water soluble diethylene glycol ether type solvents.
We have determined that it is difficult to include an alkanolamine solvent at significant levels in a liquid abrasive cleaner. It is believed that alkanolamines have both electrolyte and solvent properties and can influence the structure of the suspending phase. Consequently, as the temperature of the composition changes, on storage or during transportation, the level of effective electrolyte in the composition will also change and this can result in the p"'v~t~DED S~EE~
breakdown of the suspending phase and precipitation of abrasive particles or even phase-separation of the composition.
Brief Description of the Invention We have now determined that improved liquid abrasive cleaners of pH 7-13 can be formulated with significant levels of a CZ-C6 alkanolamine, provided that a hydrocarbon co-solvent is present. The presence of alkanolamines is desirable at the alkanolamine can act as both a solvent and as a base to assist in the removal of difficult soils.
Accordingly, the present invention provides a liquid abrasive cleaning composition of pH 7-13 which comprises:
a) 0.1-20owt of one or more surfactants forming a suspending sy s t em, b) 2-80%wt one or more suspended abrasives, c) 0.5-10%wt of a Cz-C6 alkanolamine, and, d) 0.25-10°swt of a hydrocarbon co-solvent It is believed that the alkanolamine acts both as a base and a solvent which improves cleaning and so allows the level of suspended abrasive to be reduced. In turn this is believed to reduce the possibility of abrasive damage to surfaces and improve rinsing performance. It is believed that the presence of the hydrocarbon co-solvent is required to maintain the stability of the alkanolamine based composition when it is .r.; .. ~~..:r.'..:,..,....
_T.
WO 98!49261 PCT/EP98/02276 _ 5 _ subjected to temperature cycling or storage at extremes of temperature.
Detailed Description of the Invention In order that the invention may be further understood various preferred and/or optional features of the embodiments of the invention are described below.
Alkanolamines:
Alkanolamines for use in the compositions of the present invention can be mono- or poly-functional as regards the amine and hydroxy moieties. Preferred alkanolamines are generally of the formulation H2N-R1-OH where R1 is a linear or branched alkyl chain having 2-6 carbons. Suitable alkanolamines include:
2-amino-2-methyl-1-propanol, mono- di- and tri- ethanolamine, mono-, di- and tri -isopropanolamine, and, dimethyl-, diethyl or dibutyl ethanolamine, It is envisaged that cyclic alkanolamines such as morpholine can also be employed.
Particularly suitable alkanolamines include: 2-amino-2-methyl-1-propanol, mono-ethanolamine and di-ethanolamine. These . materials are believed to give improved cleaning on tough or aged soils. Of these materials 2-amino-2-methyl-1-propanol (AMP) is particularly preferred.
WO 98/492b1 PCT/EP98/02276 Typical levels of alkanolamine in the compositions of the invention range from 1-5%wt. Higher levels of solvent are less desirable as these may attack certain plastics materials.
It is particularly preferred to use 2-amino-2-methyl-1-propanol at a level of 1-3%wt.
Co-solvents:
Suitable co-solvent include saturated and unsaturated, linear or branched hydrocarbons. Preferred materials include:
CloHl~ terpenes, and, Clo-C1~ straight chain paraffins Particularly suitable terpenes include d-limonene.
Particularly preferred paraffins include the material available in the marketplace as 'Shellsol-T' [TM].
Typical levels of co-solvent range from 0.5-5%wt. It is particularly preferred to use terpines at levels 1-3%wt. Some of these terpene materials, such as limonene, have the further advantage that they, or impurities present in them, exhibit insect-repellency. We have determined that the terpene materials give better performance at pH's below 11. The straight chain paraffins can be used at higher levels than the terpenes as these materials are less aggressive to plastics.
The paraffins are believed to give better performance at pH's above 11.
It is preferred that the ratio of the alkanolamine to the hydrocarbon co-solvent falls in the range 3:1-1:3, with ratios of 3:1 to 1:1 being particularly preferred.
_. T
Advantageously, a portion of the co-solvent can be introduced as a perfume component, although the levels of co-solvent required will generally require the addition of higher levels of this component that would normally be present as a perfume ingredient in cleaning compositions. Preferably the terpenes are used in this manner as selected terpenes, such as limonene, have a pleasant citrus smell, whereas paraffins are generally odourless.
Abrasives:
A dispersed, suspended particulate phase is an essential ingredient of compositions according to the present invention.
Preferably, the dispersed suspended particulate phase comprises a particulate abrasive which is insoluble in the aqueous phase. In the alternative, the abrasive may be soluble and present in such excess that the solubility of the abrasive in the aqueous phase is exceeded and consequently solid abrasive exists in the composition.
Preferred abrasives for use in general purpose compositions have a Moh hardness below 6 although higher hardness abrasives can be employed for specialist applications. Lower hardness materials generally give less surface damage.
Suitable abrasives can be selected from, particulate zeolites, calcites, silicas, silicates, carbonates, aluminas, bicarbonates, borates, sulphates, and, polymeric materials such as polyethylene.
_ g _ Preferred average (weight average) particle sizes for the abrasive fall in the range 0.5-200 microns, with values of around 10-100 microns being preferred. In this range an acceptable compromise between good cleaning behaviour and low S substrate damage is achieved.
Preferred levels of abrasive range from 5-70wt~ on product, preferably in the range 20-40wto, most preferably >30wt~.
Such levels of abrasive give effective cleaning and good rinsing.
The most preferred abrasives are calcium carbonate (as calcite), mixtures of calcium and magnesium carbonates (as dolomite), sodium hydrogen carbonate, potassium sulphate, zeolite, alumina, hydrated alumina, feldspar, talc and silica.
Calcite and dolomite are particularly preferred due to their low cost, suitable hardness and colour.
Surfactants:
The composition according to the invention will comprise detergent actives which are generally chosen from both anionic and nonionic detergent actives.
Suitable anionic detergent active compounds are water-soluble salts of organic sulphuric reaction products having in the molecular structure an alkyl radical containing from 8 to 22 carbon atoms, and a radical chosen from sulphonic acid or sulphur acid ester radicals and mixtures thereof.
_ ~ __ ___.._ __ T_.___._. .._ _ g _ Examples of suitable anionic detergents are sodium and potassium alcohol sulphates, especially those obtained by sulphating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; sodium and potassium alkyl benzene sulphonates such as those in which the alkyl group contains from 9 to 15 carbon atoms; sodium and potassium secondary alkanesulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulphates; sodium and potassium salts of sulphuric acid esters of the reaction product of one mole of a higher fatty alcohol and from 1 to 6 moles of ethylene oxide;
sodium and potassium salts of alkyl phenol ethylene oxide ether sulphate with from 1 to 8 units of ethylene oxide molecule and in which the alkyl radicals contain from 4 to 14 carbon atoms; the reaction product of fatty acids esterified with isethionic acid and neutralised with sodium hydroxide where, for example, the fatty acids are derived from coconut oil and mixtures thereof.
The preferred water-soluble synthetic anionic detergent active compounds are the alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and magnesium) salts of higher alkyl benzene sulphonates and mixtures with olefinsulphonates and higher alkyl sulphates, and the higher fatty acid monoglyceride sulphates. The most preferred anionic detergent active compounds are higher alkyl aromatic sulphonates such as higher alkyl benzene sulphonates containing from 6 to 20 carbon atoms in the alkyl group in a straight or branched chain, particular examples of which are sodium salts of higher alkyl benzene sulphonates or of higher-alkyl toluene, xylene or phenol sulphonates, alkyl naphthalene sulphonates, ammonium diamyl naphthalene sulphonate, and sodium dinonyl naphthalene sulphonate.
The amount of synthetic anionic detergent active to be employed in the detergent composition of this invention will generally be from 1 to 250, preferably from 2 to 200, and most preferably from 2 to 15o by weight.
Suitable nonionic detergent active compounds can be broadly described as compounds produced by the condensation of alkylene oxide groups, which are hydrophilic in nature, with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature. The length of the hydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
Particular examples include the condensation product of aliphatic alcohols having from 8 to 22 carbon atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut oil ethylene oxide condensate having from 2 to 15 moles of ethylene oxide per mole of coconut alcohol;
condensates of alkylphenols whose alkyl group contains from 6 to 12 carbon atoms with 5 to 25 moles of ethylene oxide per mole of alkylphenol; condensates of the reaction product of ethylenediamine and propylene oxide with ethylene oxide, the condensates containing from 40 to 80% of polyoxyethylene radicals by weight and having a molecular weight of from 5,000 to 11,000; tertiary amine oxides of structure R3N0, where one group R is an alkyl group of 8 to 18 carbon atoms and the others are each methyl, ethyl or hydroxyethyl groups, for instance dimethyldodecylamine oxide; tertiary phosphine oxides r. _.r -____ WO 98/49261 PC'f/EP98/02276 of structure R3P0, where one group R is an alkyl group of from to 18 carbon atoms, and the others are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, for instance dimethyldodecylphosphine oxide; and dialkyl sulphoxides of 5 structure 8250 where the group R is an alkyl group of from 10 to 18 carbon atoms and the other is methyl or ethyl, for instance methyltetradecyl sulphoxide; fatty acid alkylolamides; alkylene oxide condensates of fatty acid alkylolamides and alkyl mercaptans.
The amount of nonionic detergent active to be employed in the detergent composition of the invention will generally be from 0.5 to 150, preferably from 1 to 10%, and most preferably from 1 to 8o by weight.
Preferably, the compositions contain an amount of both the anionic and the nonionic detergent active which is chosen, bearing in mind the level of electrolyte present, so as to provide a structured liquid detergent composition, ie. one which is 'self' thickened without necessarily employing any other thickening agent.
The weight ratio of anionic detergent to nonionic detergent active may vary and will depend on their nature but is preferably in the range of from 1:9 to 9:1, ideally from 1:4 to 4:1.
According to a preferred embodiment illustrating this aspect of the invention, the detergent compositions will comprise from 2 to 10o by weight of a water-soluble, synthetic anionic sulphated or sulphonated detergent salt containing an alkyl radical having from 8 to 22 carbon atoms in the molecule, and from 0.5 to 8% by weight of an alkyleneoxylated nonionic detergent derived from the condensation of an aliphatic alcohol having from 8 to 22 carbon atoms in the molecule with ethylene oxide, such that the condensate has from 2 to 15 moles of ethylene oxide per mole of aliphatic alcohol.
It is also possible optionally to include amphoteric, cationic or zwitterionic detergent actives in the compositions according to the invention.
Suitable amphoteric detergent-active compounds that optionally can be employed are derivatives of aliphatic secondary and tertiary amines containing an alkyl group of 8 to 18 carbon atoms and an aliphatic radical substituted by an anionic water-solubilising group, for instance sodium 3-dodecylamino-propionate, sodium 3-dodecylaminopropane sulphonate and sodium N-2-hydroxydodecyl-N-methyl taurate.
Suitable cationic detergent-active compounds are quaternary ammonium salts having an aliphatic radical of from 8 to 18 carbon atoms, for instance cetyltrimethyl ammonium bromide.
Suitable zwitterionic detergent-active compounds that optionally can be employed are derivatives of aliphatic quaternary ammonium, sulphonium and phosphonium compounds having an aliphatic radical of from 8 to 18 carbon atoms and an aliphatic radical substituted by an anionic water-solubilising group, for instance 3-(N,N-dimethyl-N-hexadecylammonium)propane-1-sulphonate betaine, 3-(dodecyl methyl sulphonium) propane-1-sulphonate betaine and 3-(cetylmethyl phosphonium) ethane sulphonate betaine.
Further examples of suitable detergent-active compounds are compounds commonly used as surface-active agents given in the T__ _r __ _ well-known textbooks "Surface Active Agents", Volume I by Schwartz and Perry and "Surface Active Agents and Detergents", Volume II by Schwartz, Perry and Berch.
The total amount of detergent active compound to be employed in the detergent composition of the invention will generally be from 1.5 to 30%, preferably from 2 to 15o by weight.
It is an important feature of the invention that the composition will be capable of stably suspending the particles of abrasive, so that the consumer does not need to agitate the composition, for example by shaking it, in order to re-suspend and re-distribute sedimented particles prior to use. For this purpose, the composition should have a viscosity at 200C of at least 5000 Pas at a shear rate of 3 x 10-5 sec.-1 (as determined by Stokes Law). This viscosity is generally sufficient to ensure that the particles of abrasive do not sediment on standing at 200C by more than 1 cm in one month.
The composition according to the invention should also remain sufficiently fluid, so that it can readily be poured from a bottle or other container when required for use. For this purpose, the composition should preferably have a viscosity at 200C, measured using a rotational viscometer which does not exceed 10 Pas at a shear rate of 21 sec.-1. Preferably, the viscosity at 200C is no greater than 5 Pas at a shear rate of 21 sec-' .
Suitable rheological conditions to suit these criteria can be provided by judicial choice of anionic and nonionic detergent to provide a structured liquid having the requisite suspending properties, and/or by use of an appropriate amount of an alternative structuring agent such as is well known in the art.
Polymers:
The compositions according to the invention may optionally contain polymeric structuring agents to aid in providing appropriate rheological properties to maintain the undissolved salt or salts uniformly distributed in the composition and in enhancing their distribution and adherence of the composition to the hard surface to be cleaned.
Preferred structuring agents include polysaccharides, such as sodium carboxymethyl cellulose and other chemically modified cellulose materials, xanthan gum and other non-flocculating structuring agents such as Biopolymer PS87 referred to in US
Patent No. 4 329 448. Certain polymers such as a polymer of acrylic acid cross-linked with a poly functional agent, for example CARBOPOLR, can also be used as structuring agents. The amount of such structuring agents, when employed, to be used in compositions according to the invention can be as little as 0.001%, preferably at least 0.01% by weight of the composition.
In general, the composition of the invention can optionally comprise from 0.1-1% of polymer.
Optional Ingredients:
The composition according to the invention can contain other ingredients which aid in their cleaning performance. For _. .-T__.__.__ ~ .._......._ ___..__ __ example, the composition can contain detergent builders other than the special water-soluble salts, as defined herein, such as nitrilotriacetates, polycarboxylates, citrates, dicarboxylic acids, water-soluble phosphates especially polyphosphates, mixtures of ortho- and pyrophosphate, zeolites and mixtures thereof. Such builders can additionally function as abrasives if present in an amount in excess of their solubility in water. In general, the builder, other than the special water-soluble salts when employed, preferably will form from 0.1 to 25% by weight of the composition.
Metal ion sequestrants such as ethylenediaminetetraacetates, amino-polyphosphonates (DEQUEST~) and phosphates and a wide variety of other poly-functional organic acids and salts, can also optionally be employed provided they are compatible with the abrasive material.
A further optional ingredient for compositions according to the invention is a suds regulating material, which can be employed in compositions according to the invention which have a tendency to produce excessive suds in use. One example of a suds regulating material is soap. Soaps are salts of fatty acids and include alkali metal soaps such as the sodium, potassium and ammonium salts of higher fatty acids containing from about 8 to about 24 carbon atoms, and preferably from about 10 to about 20 carbon atoms. Particularly useful are the sodium and potassium and mono-, di- and triethanolamine salts of the mixtures of fatty acids derived from coconut oil and ground nut oil. When employed, the amount of soap can form at least 0.005%, preferably 0.5% to 2% by weight of the composition. Fatty acid soaps such as Prifac 7901 [TM] have been found to be suitable for this purpose.
A further example of a suds regulating material is an silica or a silicone oil. Where the hydrocarbons according to the present invention are present at sufficiently high levels these may themselves provide some or all of the required antifoaming activity.
Compositions according to the invention can also contain, in addition to the ingredients already mentioned, various other optional ingredients such as Colourants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly hypohalites), gel-control agents, further freeze-thaw stabilisers, bactericides, preservatives (for example 1,2, benzisothiazolin-3-one), and hydrotropes.
pH:
Compositions according to the invention are formulated in the alkaline pH range, and will generally have a pH of from 9.5 to 12.5, preferably about 10 to 12 when calcite is used as the abrasive. When other abrasives are used the pH can be lower, but the pH should generally be above the (pKa of the alkanolamine)-1 and preferably be above the pKa of the alkanolamine.
Alkalising agents such as sodium hydroxide and sodium carbonate and acids such as hydrochloric acid can be used to adjust and buffer the pH as desired.
_ T _ _. T_ Preferred Compositions:
Preferred compositions according to the present invention - comprise:
a) 1-5%wt alkali metal carbonate and/or bicarbonate, b) 1-5%wt alkyl benzene sulphonate, c) 0-1%wt fatty acid, d) 1-3%wt ethoxylated alcohol nonionic surfactant, e) 0.5-2.0%wt of an alkanolamines selected from the group comprising: 2-amino-2-methyl-1-propanol, mono- di- and tri- ethanolamine, mono-, di- and tri- isopropanolamine, dimethyl-, diethyl- or dibutyl- ethanolamine, and mixtures thereof, f) 0.5-2.0%wt of a co-solvent selected from the group comprising: CloHm terpenes, Clo-C,n straight chain paraffins and mixtures thereof, g) 20-40% of an abrasive selected from the group comprising:
calcium carbonate, magnesium carbonates, zeolite, alumina, hydrated alumina, feldspar, talc, silica and mixtures thereof, and, h) 0.1-2%wt perfume components other than terpenes, with the balance comprising minors and water.
In order that the invention may be further understood it will be described hereinafter with reference to the following non-limiting examples:
EXAMPLES
Examples were performed using the following base compositions (as given in table 1) with varying levels of solvents as indicated in table 2. Compositions were prepared at pH 10 and pH 12 as indicated in table 1.
'Base Compositions pHlO pHl2 Sodium carbonate 3.130 3.130 Sodium 0.53% 0.53%
bicarbonate I
~Calcite 35.0% 35.0% [OMY Acarb 30-AV: TM
ex. OMYA]
Alkyl Benzene 3.OOo 3.OOo [Petrelab 550: TM
Sulphonate ex. Petresa]
Coconut fatty 0.480 0.480 [Prifac 7901: TM
acid ex. Unichema]
Nonionic 7E0 1.50% 1.500 [Dobanol 23-6.5E0:
TM ex. Shell]
Hydrochloric acid 0.26% - [2M ex. Fisons]
Sodium Hydroxide - 0.420 1,2,Benzisothiazo .016% .0160 [Proxel GXL: TM ex.
lin-3-one ICI]
Perfume 0.50% 0.50% [CL0318A: TM ex.
Quest]
Water to 100% to 100%
r _-____ _.__T _ ____. _.__ Using the compositions of table 1, the examples of table 2 below were made up adding a total of 2% solvent which was either 2% amino-methyl propanol (AMP) or 1% amino methyl propanol plus a co-solvent. The stability of the compositions was determined during five weeks storage under ambient conditions and under various modified temperature conditions.
The modified temperature conditions were:
a) Ten freeze-thaw cycles with sixteen hours at below -15 Celsius and 8 hours at 25 Celsius.
b) Five weeks storage at 4 degrees Celsius.
c) Five weeks storage at 37 degrees Celsius.
Failure marked in the columns headed 'temp' in table 2 indicates that the samples separated into two or more phases when stored under at least one of the modified temperature conditions. Failure marked in the column headed 'ambi' in table 2 indicates that the samples separated into two or more phases when stored under ambient conditions. The examples with Shellsol T and limonene are embodiments of the invention the examples with benzyl alcohol, Butyl Digol [TM] (diethylene glycol mono n-butyl ether) and Dowanol PnB [TM] (propylene glycol mono n-butyl ether) are comparatives which show that not all solvents are suitable for use in the practice of the invention.
TABLE 2: Storacre Results Composition pHlO pHlO pHl2 pHl2 Ambi Temp Ambi Temp Base 2%AMP pass fail pass fail +
Base 1oAMP to She11So1 T pass pass fail fail + +
Base 1%AMP 1% limonene fail fail pass pass + +
Base 1%AMP 1% Dowanol PnB pass fail fail fail + +
Base 1%AMP 1% Benzyl fail fail pass fail + +
alcohol Base 1%AMP 1o Butyl Digol fail fail fail fail + +
From the above results it can be seen that stable compositions at pH 10 could be made using paraffin (Shellsol T) as the co-solvent. At higher pH limonene was effective as a co-solvent.
The compositions with ShellSoL-T and limonene both showed acceptable cleaning performance on tough soils. The compositions prepared with the Dowanol PnB, benzyl alcohol and Butyl Digol all showed instability under one or more conditions of storage at other than ambient temperature.
T _.__-.~.~~ ~
Brief Description of the Invention We have now determined that improved liquid abrasive cleaners of pH 7-13 can be formulated with significant levels of a CZ-C6 alkanolamine, provided that a hydrocarbon co-solvent is present. The presence of alkanolamines is desirable at the alkanolamine can act as both a solvent and as a base to assist in the removal of difficult soils.
Accordingly, the present invention provides a liquid abrasive cleaning composition of pH 7-13 which comprises:
a) 0.1-20owt of one or more surfactants forming a suspending sy s t em, b) 2-80%wt one or more suspended abrasives, c) 0.5-10%wt of a Cz-C6 alkanolamine, and, d) 0.25-10°swt of a hydrocarbon co-solvent It is believed that the alkanolamine acts both as a base and a solvent which improves cleaning and so allows the level of suspended abrasive to be reduced. In turn this is believed to reduce the possibility of abrasive damage to surfaces and improve rinsing performance. It is believed that the presence of the hydrocarbon co-solvent is required to maintain the stability of the alkanolamine based composition when it is .r.; .. ~~..:r.'..:,..,....
_T.
WO 98!49261 PCT/EP98/02276 _ 5 _ subjected to temperature cycling or storage at extremes of temperature.
Detailed Description of the Invention In order that the invention may be further understood various preferred and/or optional features of the embodiments of the invention are described below.
Alkanolamines:
Alkanolamines for use in the compositions of the present invention can be mono- or poly-functional as regards the amine and hydroxy moieties. Preferred alkanolamines are generally of the formulation H2N-R1-OH where R1 is a linear or branched alkyl chain having 2-6 carbons. Suitable alkanolamines include:
2-amino-2-methyl-1-propanol, mono- di- and tri- ethanolamine, mono-, di- and tri -isopropanolamine, and, dimethyl-, diethyl or dibutyl ethanolamine, It is envisaged that cyclic alkanolamines such as morpholine can also be employed.
Particularly suitable alkanolamines include: 2-amino-2-methyl-1-propanol, mono-ethanolamine and di-ethanolamine. These . materials are believed to give improved cleaning on tough or aged soils. Of these materials 2-amino-2-methyl-1-propanol (AMP) is particularly preferred.
WO 98/492b1 PCT/EP98/02276 Typical levels of alkanolamine in the compositions of the invention range from 1-5%wt. Higher levels of solvent are less desirable as these may attack certain plastics materials.
It is particularly preferred to use 2-amino-2-methyl-1-propanol at a level of 1-3%wt.
Co-solvents:
Suitable co-solvent include saturated and unsaturated, linear or branched hydrocarbons. Preferred materials include:
CloHl~ terpenes, and, Clo-C1~ straight chain paraffins Particularly suitable terpenes include d-limonene.
Particularly preferred paraffins include the material available in the marketplace as 'Shellsol-T' [TM].
Typical levels of co-solvent range from 0.5-5%wt. It is particularly preferred to use terpines at levels 1-3%wt. Some of these terpene materials, such as limonene, have the further advantage that they, or impurities present in them, exhibit insect-repellency. We have determined that the terpene materials give better performance at pH's below 11. The straight chain paraffins can be used at higher levels than the terpenes as these materials are less aggressive to plastics.
The paraffins are believed to give better performance at pH's above 11.
It is preferred that the ratio of the alkanolamine to the hydrocarbon co-solvent falls in the range 3:1-1:3, with ratios of 3:1 to 1:1 being particularly preferred.
_. T
Advantageously, a portion of the co-solvent can be introduced as a perfume component, although the levels of co-solvent required will generally require the addition of higher levels of this component that would normally be present as a perfume ingredient in cleaning compositions. Preferably the terpenes are used in this manner as selected terpenes, such as limonene, have a pleasant citrus smell, whereas paraffins are generally odourless.
Abrasives:
A dispersed, suspended particulate phase is an essential ingredient of compositions according to the present invention.
Preferably, the dispersed suspended particulate phase comprises a particulate abrasive which is insoluble in the aqueous phase. In the alternative, the abrasive may be soluble and present in such excess that the solubility of the abrasive in the aqueous phase is exceeded and consequently solid abrasive exists in the composition.
Preferred abrasives for use in general purpose compositions have a Moh hardness below 6 although higher hardness abrasives can be employed for specialist applications. Lower hardness materials generally give less surface damage.
Suitable abrasives can be selected from, particulate zeolites, calcites, silicas, silicates, carbonates, aluminas, bicarbonates, borates, sulphates, and, polymeric materials such as polyethylene.
_ g _ Preferred average (weight average) particle sizes for the abrasive fall in the range 0.5-200 microns, with values of around 10-100 microns being preferred. In this range an acceptable compromise between good cleaning behaviour and low S substrate damage is achieved.
Preferred levels of abrasive range from 5-70wt~ on product, preferably in the range 20-40wto, most preferably >30wt~.
Such levels of abrasive give effective cleaning and good rinsing.
The most preferred abrasives are calcium carbonate (as calcite), mixtures of calcium and magnesium carbonates (as dolomite), sodium hydrogen carbonate, potassium sulphate, zeolite, alumina, hydrated alumina, feldspar, talc and silica.
Calcite and dolomite are particularly preferred due to their low cost, suitable hardness and colour.
Surfactants:
The composition according to the invention will comprise detergent actives which are generally chosen from both anionic and nonionic detergent actives.
Suitable anionic detergent active compounds are water-soluble salts of organic sulphuric reaction products having in the molecular structure an alkyl radical containing from 8 to 22 carbon atoms, and a radical chosen from sulphonic acid or sulphur acid ester radicals and mixtures thereof.
_ ~ __ ___.._ __ T_.___._. .._ _ g _ Examples of suitable anionic detergents are sodium and potassium alcohol sulphates, especially those obtained by sulphating the higher alcohols produced by reducing the glycerides of tallow or coconut oil; sodium and potassium alkyl benzene sulphonates such as those in which the alkyl group contains from 9 to 15 carbon atoms; sodium and potassium secondary alkanesulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulphates; sodium and potassium salts of sulphuric acid esters of the reaction product of one mole of a higher fatty alcohol and from 1 to 6 moles of ethylene oxide;
sodium and potassium salts of alkyl phenol ethylene oxide ether sulphate with from 1 to 8 units of ethylene oxide molecule and in which the alkyl radicals contain from 4 to 14 carbon atoms; the reaction product of fatty acids esterified with isethionic acid and neutralised with sodium hydroxide where, for example, the fatty acids are derived from coconut oil and mixtures thereof.
The preferred water-soluble synthetic anionic detergent active compounds are the alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and magnesium) salts of higher alkyl benzene sulphonates and mixtures with olefinsulphonates and higher alkyl sulphates, and the higher fatty acid monoglyceride sulphates. The most preferred anionic detergent active compounds are higher alkyl aromatic sulphonates such as higher alkyl benzene sulphonates containing from 6 to 20 carbon atoms in the alkyl group in a straight or branched chain, particular examples of which are sodium salts of higher alkyl benzene sulphonates or of higher-alkyl toluene, xylene or phenol sulphonates, alkyl naphthalene sulphonates, ammonium diamyl naphthalene sulphonate, and sodium dinonyl naphthalene sulphonate.
The amount of synthetic anionic detergent active to be employed in the detergent composition of this invention will generally be from 1 to 250, preferably from 2 to 200, and most preferably from 2 to 15o by weight.
Suitable nonionic detergent active compounds can be broadly described as compounds produced by the condensation of alkylene oxide groups, which are hydrophilic in nature, with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature. The length of the hydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
Particular examples include the condensation product of aliphatic alcohols having from 8 to 22 carbon atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut oil ethylene oxide condensate having from 2 to 15 moles of ethylene oxide per mole of coconut alcohol;
condensates of alkylphenols whose alkyl group contains from 6 to 12 carbon atoms with 5 to 25 moles of ethylene oxide per mole of alkylphenol; condensates of the reaction product of ethylenediamine and propylene oxide with ethylene oxide, the condensates containing from 40 to 80% of polyoxyethylene radicals by weight and having a molecular weight of from 5,000 to 11,000; tertiary amine oxides of structure R3N0, where one group R is an alkyl group of 8 to 18 carbon atoms and the others are each methyl, ethyl or hydroxyethyl groups, for instance dimethyldodecylamine oxide; tertiary phosphine oxides r. _.r -____ WO 98/49261 PC'f/EP98/02276 of structure R3P0, where one group R is an alkyl group of from to 18 carbon atoms, and the others are each alkyl or hydroxyalkyl groups of 1 to 3 carbon atoms, for instance dimethyldodecylphosphine oxide; and dialkyl sulphoxides of 5 structure 8250 where the group R is an alkyl group of from 10 to 18 carbon atoms and the other is methyl or ethyl, for instance methyltetradecyl sulphoxide; fatty acid alkylolamides; alkylene oxide condensates of fatty acid alkylolamides and alkyl mercaptans.
The amount of nonionic detergent active to be employed in the detergent composition of the invention will generally be from 0.5 to 150, preferably from 1 to 10%, and most preferably from 1 to 8o by weight.
Preferably, the compositions contain an amount of both the anionic and the nonionic detergent active which is chosen, bearing in mind the level of electrolyte present, so as to provide a structured liquid detergent composition, ie. one which is 'self' thickened without necessarily employing any other thickening agent.
The weight ratio of anionic detergent to nonionic detergent active may vary and will depend on their nature but is preferably in the range of from 1:9 to 9:1, ideally from 1:4 to 4:1.
According to a preferred embodiment illustrating this aspect of the invention, the detergent compositions will comprise from 2 to 10o by weight of a water-soluble, synthetic anionic sulphated or sulphonated detergent salt containing an alkyl radical having from 8 to 22 carbon atoms in the molecule, and from 0.5 to 8% by weight of an alkyleneoxylated nonionic detergent derived from the condensation of an aliphatic alcohol having from 8 to 22 carbon atoms in the molecule with ethylene oxide, such that the condensate has from 2 to 15 moles of ethylene oxide per mole of aliphatic alcohol.
It is also possible optionally to include amphoteric, cationic or zwitterionic detergent actives in the compositions according to the invention.
Suitable amphoteric detergent-active compounds that optionally can be employed are derivatives of aliphatic secondary and tertiary amines containing an alkyl group of 8 to 18 carbon atoms and an aliphatic radical substituted by an anionic water-solubilising group, for instance sodium 3-dodecylamino-propionate, sodium 3-dodecylaminopropane sulphonate and sodium N-2-hydroxydodecyl-N-methyl taurate.
Suitable cationic detergent-active compounds are quaternary ammonium salts having an aliphatic radical of from 8 to 18 carbon atoms, for instance cetyltrimethyl ammonium bromide.
Suitable zwitterionic detergent-active compounds that optionally can be employed are derivatives of aliphatic quaternary ammonium, sulphonium and phosphonium compounds having an aliphatic radical of from 8 to 18 carbon atoms and an aliphatic radical substituted by an anionic water-solubilising group, for instance 3-(N,N-dimethyl-N-hexadecylammonium)propane-1-sulphonate betaine, 3-(dodecyl methyl sulphonium) propane-1-sulphonate betaine and 3-(cetylmethyl phosphonium) ethane sulphonate betaine.
Further examples of suitable detergent-active compounds are compounds commonly used as surface-active agents given in the T__ _r __ _ well-known textbooks "Surface Active Agents", Volume I by Schwartz and Perry and "Surface Active Agents and Detergents", Volume II by Schwartz, Perry and Berch.
The total amount of detergent active compound to be employed in the detergent composition of the invention will generally be from 1.5 to 30%, preferably from 2 to 15o by weight.
It is an important feature of the invention that the composition will be capable of stably suspending the particles of abrasive, so that the consumer does not need to agitate the composition, for example by shaking it, in order to re-suspend and re-distribute sedimented particles prior to use. For this purpose, the composition should have a viscosity at 200C of at least 5000 Pas at a shear rate of 3 x 10-5 sec.-1 (as determined by Stokes Law). This viscosity is generally sufficient to ensure that the particles of abrasive do not sediment on standing at 200C by more than 1 cm in one month.
The composition according to the invention should also remain sufficiently fluid, so that it can readily be poured from a bottle or other container when required for use. For this purpose, the composition should preferably have a viscosity at 200C, measured using a rotational viscometer which does not exceed 10 Pas at a shear rate of 21 sec.-1. Preferably, the viscosity at 200C is no greater than 5 Pas at a shear rate of 21 sec-' .
Suitable rheological conditions to suit these criteria can be provided by judicial choice of anionic and nonionic detergent to provide a structured liquid having the requisite suspending properties, and/or by use of an appropriate amount of an alternative structuring agent such as is well known in the art.
Polymers:
The compositions according to the invention may optionally contain polymeric structuring agents to aid in providing appropriate rheological properties to maintain the undissolved salt or salts uniformly distributed in the composition and in enhancing their distribution and adherence of the composition to the hard surface to be cleaned.
Preferred structuring agents include polysaccharides, such as sodium carboxymethyl cellulose and other chemically modified cellulose materials, xanthan gum and other non-flocculating structuring agents such as Biopolymer PS87 referred to in US
Patent No. 4 329 448. Certain polymers such as a polymer of acrylic acid cross-linked with a poly functional agent, for example CARBOPOLR, can also be used as structuring agents. The amount of such structuring agents, when employed, to be used in compositions according to the invention can be as little as 0.001%, preferably at least 0.01% by weight of the composition.
In general, the composition of the invention can optionally comprise from 0.1-1% of polymer.
Optional Ingredients:
The composition according to the invention can contain other ingredients which aid in their cleaning performance. For _. .-T__.__.__ ~ .._......._ ___..__ __ example, the composition can contain detergent builders other than the special water-soluble salts, as defined herein, such as nitrilotriacetates, polycarboxylates, citrates, dicarboxylic acids, water-soluble phosphates especially polyphosphates, mixtures of ortho- and pyrophosphate, zeolites and mixtures thereof. Such builders can additionally function as abrasives if present in an amount in excess of their solubility in water. In general, the builder, other than the special water-soluble salts when employed, preferably will form from 0.1 to 25% by weight of the composition.
Metal ion sequestrants such as ethylenediaminetetraacetates, amino-polyphosphonates (DEQUEST~) and phosphates and a wide variety of other poly-functional organic acids and salts, can also optionally be employed provided they are compatible with the abrasive material.
A further optional ingredient for compositions according to the invention is a suds regulating material, which can be employed in compositions according to the invention which have a tendency to produce excessive suds in use. One example of a suds regulating material is soap. Soaps are salts of fatty acids and include alkali metal soaps such as the sodium, potassium and ammonium salts of higher fatty acids containing from about 8 to about 24 carbon atoms, and preferably from about 10 to about 20 carbon atoms. Particularly useful are the sodium and potassium and mono-, di- and triethanolamine salts of the mixtures of fatty acids derived from coconut oil and ground nut oil. When employed, the amount of soap can form at least 0.005%, preferably 0.5% to 2% by weight of the composition. Fatty acid soaps such as Prifac 7901 [TM] have been found to be suitable for this purpose.
A further example of a suds regulating material is an silica or a silicone oil. Where the hydrocarbons according to the present invention are present at sufficiently high levels these may themselves provide some or all of the required antifoaming activity.
Compositions according to the invention can also contain, in addition to the ingredients already mentioned, various other optional ingredients such as Colourants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly hypohalites), gel-control agents, further freeze-thaw stabilisers, bactericides, preservatives (for example 1,2, benzisothiazolin-3-one), and hydrotropes.
pH:
Compositions according to the invention are formulated in the alkaline pH range, and will generally have a pH of from 9.5 to 12.5, preferably about 10 to 12 when calcite is used as the abrasive. When other abrasives are used the pH can be lower, but the pH should generally be above the (pKa of the alkanolamine)-1 and preferably be above the pKa of the alkanolamine.
Alkalising agents such as sodium hydroxide and sodium carbonate and acids such as hydrochloric acid can be used to adjust and buffer the pH as desired.
_ T _ _. T_ Preferred Compositions:
Preferred compositions according to the present invention - comprise:
a) 1-5%wt alkali metal carbonate and/or bicarbonate, b) 1-5%wt alkyl benzene sulphonate, c) 0-1%wt fatty acid, d) 1-3%wt ethoxylated alcohol nonionic surfactant, e) 0.5-2.0%wt of an alkanolamines selected from the group comprising: 2-amino-2-methyl-1-propanol, mono- di- and tri- ethanolamine, mono-, di- and tri- isopropanolamine, dimethyl-, diethyl- or dibutyl- ethanolamine, and mixtures thereof, f) 0.5-2.0%wt of a co-solvent selected from the group comprising: CloHm terpenes, Clo-C,n straight chain paraffins and mixtures thereof, g) 20-40% of an abrasive selected from the group comprising:
calcium carbonate, magnesium carbonates, zeolite, alumina, hydrated alumina, feldspar, talc, silica and mixtures thereof, and, h) 0.1-2%wt perfume components other than terpenes, with the balance comprising minors and water.
In order that the invention may be further understood it will be described hereinafter with reference to the following non-limiting examples:
EXAMPLES
Examples were performed using the following base compositions (as given in table 1) with varying levels of solvents as indicated in table 2. Compositions were prepared at pH 10 and pH 12 as indicated in table 1.
'Base Compositions pHlO pHl2 Sodium carbonate 3.130 3.130 Sodium 0.53% 0.53%
bicarbonate I
~Calcite 35.0% 35.0% [OMY Acarb 30-AV: TM
ex. OMYA]
Alkyl Benzene 3.OOo 3.OOo [Petrelab 550: TM
Sulphonate ex. Petresa]
Coconut fatty 0.480 0.480 [Prifac 7901: TM
acid ex. Unichema]
Nonionic 7E0 1.50% 1.500 [Dobanol 23-6.5E0:
TM ex. Shell]
Hydrochloric acid 0.26% - [2M ex. Fisons]
Sodium Hydroxide - 0.420 1,2,Benzisothiazo .016% .0160 [Proxel GXL: TM ex.
lin-3-one ICI]
Perfume 0.50% 0.50% [CL0318A: TM ex.
Quest]
Water to 100% to 100%
r _-____ _.__T _ ____. _.__ Using the compositions of table 1, the examples of table 2 below were made up adding a total of 2% solvent which was either 2% amino-methyl propanol (AMP) or 1% amino methyl propanol plus a co-solvent. The stability of the compositions was determined during five weeks storage under ambient conditions and under various modified temperature conditions.
The modified temperature conditions were:
a) Ten freeze-thaw cycles with sixteen hours at below -15 Celsius and 8 hours at 25 Celsius.
b) Five weeks storage at 4 degrees Celsius.
c) Five weeks storage at 37 degrees Celsius.
Failure marked in the columns headed 'temp' in table 2 indicates that the samples separated into two or more phases when stored under at least one of the modified temperature conditions. Failure marked in the column headed 'ambi' in table 2 indicates that the samples separated into two or more phases when stored under ambient conditions. The examples with Shellsol T and limonene are embodiments of the invention the examples with benzyl alcohol, Butyl Digol [TM] (diethylene glycol mono n-butyl ether) and Dowanol PnB [TM] (propylene glycol mono n-butyl ether) are comparatives which show that not all solvents are suitable for use in the practice of the invention.
TABLE 2: Storacre Results Composition pHlO pHlO pHl2 pHl2 Ambi Temp Ambi Temp Base 2%AMP pass fail pass fail +
Base 1oAMP to She11So1 T pass pass fail fail + +
Base 1%AMP 1% limonene fail fail pass pass + +
Base 1%AMP 1% Dowanol PnB pass fail fail fail + +
Base 1%AMP 1% Benzyl fail fail pass fail + +
alcohol Base 1%AMP 1o Butyl Digol fail fail fail fail + +
From the above results it can be seen that stable compositions at pH 10 could be made using paraffin (Shellsol T) as the co-solvent. At higher pH limonene was effective as a co-solvent.
The compositions with ShellSoL-T and limonene both showed acceptable cleaning performance on tough soils. The compositions prepared with the Dowanol PnB, benzyl alcohol and Butyl Digol all showed instability under one or more conditions of storage at other than ambient temperature.
T _.__-.~.~~ ~
Claims (9)
1. A liquid abrasive cleaning composition of pH 7-13 which comprises:
a) 0.1-20%wt of one or more surfactants forming a suspending system, b) 2-80%wt one or more suspended abrasives, c) 0.5-10%wt of a C2-C6 alkanolamine, and, d) 0.25-10%wt of a hydrocarbon co-solvent
a) 0.1-20%wt of one or more surfactants forming a suspending system, b) 2-80%wt one or more suspended abrasives, c) 0.5-10%wt of a C2-C6 alkanolamine, and, d) 0.25-10%wt of a hydrocarbon co-solvent
2. A composition according to claim 1 wherein the alkanolamine is selected from the group comprising:
2-amino-2-methyl-1-propanol, mono- di- and tri-ethanolamine, mono-, di- and tri- isopropanolamine, dimethyl-, diethyl- or dibutyl- ethanolamine, and mixtures thereof.
2-amino-2-methyl-1-propanol, mono- di- and tri-ethanolamine, mono-, di- and tri- isopropanolamine, dimethyl-, diethyl- or dibutyl- ethanolamine, and mixtures thereof.
3. A composition according to claim 1 wherein the co-solvent is selected from the group comprising: C10H16 terpenes, C10-C16 straight chain paraffins and mixtures thereof.
4. A composition according to claim 1 wherein the abrasive is selected from the group comprising: calcium carbonate, magnesium carbonates, zeolite, alumina, hydrated alumina, feldspar, talc, silica and mixtures thereof.
5. A composition according to claim 1 wherein the ratio of the alkanolamine to the hydrocarbon co-solvent falls in the range 3:1-1:3.
6. A composition according to claim 1 wherein the level of abrasive is 20-40wt% on product.
7. A composition according to claim 1 which has a viscosity at 200C of at least 5000 Pas at a shear rate of 3 x 10-5 sec.-1 as determined by Stokes Law and a viscosity at 200C, measured using a rotational viscometer which does not exceed 10 Pas at a shear rate of 21 sec.-1.
8. A composition according to claim 1 having a pH of from 9.5 to 12.5.
9. A composition according to claim 1 which comprises:
a) 1-5%wt alkali metal carbonate and/or bicarbonate, b) 1-5%wt alkyl benzene sulphonate, c) 0-1%wt fatty acid, d) 1-3%wt ethoxylated alcohol nonionic surfactant, e) 0.5-2.0%wt of an alkanolamines selected from the group comprising: 2-amino-2-methyl-1-propanol, mono- di- and tri- ethanolamine, mono-, di- and tri-isopropanolamine, dimethyl-, diethyl- or dibutyl-ethanolamine, and mixtures thereof, f) 0.5-2.0%wt of a co-solvent selected from the group comprising: C10H16 terpenes, C10-C16 straight chain paraffins and mixtures thereof, g) 20-40% of an abrasive selected from the group comprising: calcium carbonate, magnesium carbonates, zeolite, alumina, hydrated alumina, feldspar, talc, silica and mixtures thereof, and, h) 0.1-2%wt perfume components other than terpenes, with the balance comprising minors and water.
a) 1-5%wt alkali metal carbonate and/or bicarbonate, b) 1-5%wt alkyl benzene sulphonate, c) 0-1%wt fatty acid, d) 1-3%wt ethoxylated alcohol nonionic surfactant, e) 0.5-2.0%wt of an alkanolamines selected from the group comprising: 2-amino-2-methyl-1-propanol, mono- di- and tri- ethanolamine, mono-, di- and tri-isopropanolamine, dimethyl-, diethyl- or dibutyl-ethanolamine, and mixtures thereof, f) 0.5-2.0%wt of a co-solvent selected from the group comprising: C10H16 terpenes, C10-C16 straight chain paraffins and mixtures thereof, g) 20-40% of an abrasive selected from the group comprising: calcium carbonate, magnesium carbonates, zeolite, alumina, hydrated alumina, feldspar, talc, silica and mixtures thereof, and, h) 0.1-2%wt perfume components other than terpenes, with the balance comprising minors and water.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9708500.5 | 1997-04-23 | ||
| GBGB9708500.5A GB9708500D0 (en) | 1997-04-25 | 1997-04-25 | Abrasive cleaning composition |
| PCT/EP1998/002276 WO1998049261A1 (en) | 1997-04-25 | 1998-04-17 | Abrasive cleaning composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2287233A1 true CA2287233A1 (en) | 1998-11-05 |
Family
ID=10811419
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002287233A Abandoned CA2287233A1 (en) | 1997-04-23 | 1998-04-17 | Abrasive cleaning composition |
Country Status (18)
| Country | Link |
|---|---|
| EP (1) | EP0977826A1 (en) |
| JP (1) | JP2001522393A (en) |
| KR (1) | KR20010012114A (en) |
| CN (1) | CN1261399A (en) |
| AR (1) | AR015597A1 (en) |
| AU (1) | AU7644898A (en) |
| BR (1) | BR9808969A (en) |
| CA (1) | CA2287233A1 (en) |
| GB (1) | GB9708500D0 (en) |
| HU (1) | HUP0004833A2 (en) |
| ID (1) | ID23146A (en) |
| IL (1) | IL132536A0 (en) |
| PL (1) | PL336419A1 (en) |
| SK (1) | SK145799A3 (en) |
| TR (1) | TR199902656T2 (en) |
| TW (1) | TW517084B (en) |
| WO (1) | WO1998049261A1 (en) |
| ZA (1) | ZA983392B (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9821784D0 (en) * | 1998-10-06 | 1998-12-02 | Unilever Plc | Non-liquid abrasive composition |
| CN1218026C (en) * | 2000-04-05 | 2005-09-07 | 荷兰联合利华有限公司 | Solid dispersible abrasive compositions |
| ES2261737T3 (en) * | 2001-10-05 | 2006-11-16 | Unilever N.V. | ABRASIVE CLEANING LIQUID COMPOSITIONS. |
| KR20030039714A (en) * | 2001-11-14 | 2003-05-22 | 김원진 | Washing lotion for spectacle lenses that are manufactured using high polymer resin and manufacture mold |
| DK2281853T3 (en) * | 2009-08-05 | 2012-07-23 | Omya Development Ag | Use of 2-amino-2-methyl-1-propanol as an additive in aqueous suspensions of materials containing calcium carbonate |
| SI2354191T1 (en) * | 2010-01-25 | 2013-08-30 | Omya Development Ag | Use of 2-((1-methylpropyl)amino)ethanol as additive in aqueous suspensions of calcium carbonate-comprising materials |
| ES2411109T3 (en) * | 2010-06-07 | 2013-07-04 | Omya Development Ag | Use of 2-aminoethanol as an additive in aqueous suspensions of materials comprising calcium carbonate |
| SI2402167T1 (en) | 2010-07-02 | 2014-01-31 | Omya International Ag | Paper for inkjet recording |
| JP5544256B2 (en) * | 2010-09-21 | 2014-07-09 | 花王株式会社 | Hard surface cleaning method |
| GB201300584D0 (en) | 2013-01-14 | 2013-02-27 | Reckitt Benckiser Brands Ltd | Antimicrobial abrasive cream type cleaning compositions for inanimate hard surfaces |
| EP3116985B1 (en) | 2014-03-12 | 2018-07-25 | The Procter and Gamble Company | Detergent composition |
| CN104120044A (en) * | 2014-06-27 | 2014-10-29 | 滁州斯迈特复合材料有限公司 | Detergent for face cream box |
| CN107287040A (en) * | 2016-03-31 | 2017-10-24 | 比亚迪股份有限公司 | A kind of radiator cleaning agent and preparation method thereof |
| WO2023041471A1 (en) * | 2021-09-14 | 2023-03-23 | Unilever Ip Holdings B.V. | An alkaline hard surface cleaning composition |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1109892A (en) * | 1965-03-12 | 1968-04-18 | Marshall Wolverhampton | A new or improved metal polishing composition |
| CH642104A5 (en) * | 1979-06-27 | 1984-03-30 | Sandoz Ag | PASTE CLEANER. |
| GB8628200D0 (en) * | 1986-11-26 | 1986-12-31 | Procter & Gamble | Creamy scouring compositions |
| IN185580B (en) * | 1991-08-30 | 2001-03-03 | Albright & Wilson Uk Ltd | |
| DE69320355T2 (en) * | 1992-09-09 | 1999-02-11 | Unilever Nv | IMPROVING CLEANERS FOR HARD SURFACES |
-
1997
- 1997-04-25 GB GBGB9708500.5A patent/GB9708500D0/en active Pending
-
1998
- 1998-04-14 IL IL13253698A patent/IL132536A0/en unknown
- 1998-04-17 HU HU0004833A patent/HUP0004833A2/en unknown
- 1998-04-17 KR KR1019997009858A patent/KR20010012114A/en not_active Application Discontinuation
- 1998-04-17 ID IDW991265A patent/ID23146A/en unknown
- 1998-04-17 EP EP98924136A patent/EP0977826A1/en not_active Withdrawn
- 1998-04-17 BR BR9808969-2A patent/BR9808969A/en not_active Application Discontinuation
- 1998-04-17 CN CN98806384A patent/CN1261399A/en active Pending
- 1998-04-17 PL PL98336419A patent/PL336419A1/en unknown
- 1998-04-17 SK SK1457-99A patent/SK145799A3/en unknown
- 1998-04-17 JP JP54654898A patent/JP2001522393A/en active Pending
- 1998-04-17 CA CA002287233A patent/CA2287233A1/en not_active Abandoned
- 1998-04-17 AU AU76448/98A patent/AU7644898A/en not_active Abandoned
- 1998-04-17 TR TR1999/02656T patent/TR199902656T2/en unknown
- 1998-04-17 WO PCT/EP1998/002276 patent/WO1998049261A1/en not_active Application Discontinuation
- 1998-04-22 ZA ZA9803392A patent/ZA983392B/en unknown
- 1998-04-24 AR ARP980101901A patent/AR015597A1/en unknown
- 1998-05-15 TW TW087107565A patent/TW517084B/en active
Also Published As
| Publication number | Publication date |
|---|---|
| JP2001522393A (en) | 2001-11-13 |
| TW517084B (en) | 2003-01-11 |
| AR015597A1 (en) | 2001-05-16 |
| EP0977826A1 (en) | 2000-02-09 |
| IL132536A0 (en) | 2001-03-19 |
| ZA983392B (en) | 1999-10-22 |
| TR199902656T2 (en) | 2000-06-21 |
| KR20010012114A (en) | 2001-02-15 |
| AU7644898A (en) | 1998-11-24 |
| WO1998049261A1 (en) | 1998-11-05 |
| PL336419A1 (en) | 2000-06-19 |
| GB9708500D0 (en) | 1997-06-18 |
| CN1261399A (en) | 2000-07-26 |
| HUP0004833A2 (en) | 2001-05-28 |
| BR9808969A (en) | 2000-08-01 |
| ID23146A (en) | 2000-03-23 |
| SK145799A3 (en) | 2000-05-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU601067B2 (en) | Liquid detergent compositions | |
| AU701587B2 (en) | Detergent composition | |
| CA2287233A1 (en) | Abrasive cleaning composition | |
| AU2002220627B2 (en) | Composition for cleaning hard surfaces | |
| CA1286188C (en) | Liquid detergent composition | |
| AU698794B2 (en) | Hard surface cleaning compositions comprising polymers | |
| AU635092B2 (en) | Cleaning composition | |
| CA1332908C (en) | Creamy scouring compositions | |
| CN1354784A (en) | Detergent composition | |
| AU688033B2 (en) | Aqueous liquid detergent compositions containing deflocculating polymers | |
| WO1998058045A1 (en) | Abrasive cleaning composition | |
| WO2000020545A1 (en) | Hard surface cleaning bar | |
| CA2073829A1 (en) | Cleaning composition | |
| CA2291002A1 (en) | Polymeric materials | |
| CZ9903785A3 (en) | Liquid abrasive cleansing agent | |
| WO2016209784A1 (en) | Low solvent liquid detergent compositions | |
| WO2000020544A1 (en) | Non-liquid abrasive composition | |
| CA2064900C (en) | Liquid detergents | |
| MXPA99011652A (en) | Granular detergent compositions and their production |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |