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WO1998058045A1 - Composition de nettoyage abrasive - Google Patents

Composition de nettoyage abrasive Download PDF

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Publication number
WO1998058045A1
WO1998058045A1 PCT/EP1998/002986 EP9802986W WO9858045A1 WO 1998058045 A1 WO1998058045 A1 WO 1998058045A1 EP 9802986 W EP9802986 W EP 9802986W WO 9858045 A1 WO9858045 A1 WO 9858045A1
Authority
WO
WIPO (PCT)
Prior art keywords
abrasive
water
composition according
alkanolamine
mixtures
Prior art date
Application number
PCT/EP1998/002986
Other languages
English (en)
Inventor
George Kerr Rennie
Patricia Revell
Original Assignee
Unilever Plc
Unilever Nv
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Unilever Plc, Unilever Nv filed Critical Unilever Plc
Priority to JP50364199A priority Critical patent/JP2002510346A/ja
Priority to IL13356798A priority patent/IL133567A0/xx
Priority to PL98337460A priority patent/PL337460A1/xx
Priority to SK1790-99A priority patent/SK179099A3/sk
Priority to CA002294204A priority patent/CA2294204A1/fr
Priority to BR9810178-1A priority patent/BR9810178A/pt
Priority to AU80194/98A priority patent/AU8019498A/en
Priority to EP98928304A priority patent/EP0991744A1/fr
Publication of WO1998058045A1 publication Critical patent/WO1998058045A1/fr

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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
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2068—Ethers
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/044—Hydroxides or bases
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/10—Carbonates ; Bicarbonates
    • 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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/14—Fillers; Abrasives ; Abrasive compositions; Suspending or absorbing agents not provided for in one single group of C11D3/12; Specific features concerning abrasives, e.g. granulometry or mixtures
    • 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

Definitions

  • the invention relates to non-liquid, abrasive, compositions containing a particulate abrasive which are suited to the cleaning of hard surfaces.
  • 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.
  • Surfactants employed 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 generally used to form a suspending system as is well known in the art.
  • Solvents are well known components of non-abrasive cleaning compositions. Typical solvents used in cleaning compositions include, alcohols (such as ethanol) , ethers,
  • EP503219A (P&G) relates to a cleaning composition containing 0.1 - 10% of an alkanolamine.
  • Non-liquid abrasive compositions are also known. These take the form of pastes, gels and powders. These may contain surfactants and may contain relatively low levels of water. Typical abrasives used in these compositions include, calcites and dolomites.
  • abrasive cleaners can be formulated with significant levels of a C 2 -C 6 alkanolamine and an electrolyte base other than alkanolamine.
  • the presence of alkanolamines is desirable as at elevated pH due to the base the alkanolamine can act as both a solvent and as a further base to assist in the removal of difficult soils.
  • the present invention provides a abrasive cleaner which effectively cleans and is stable on storage.
  • the present invention provides a non-liquid abrasive cleaning composition which comprises
  • e optionally, 0.1-20%wt of a solvent other than water or alkanolamine It is believed that, in the presence of water, i.e. during use, the combination of the base and the alkanolamine improves cleaning.
  • the invention also extends to a method of light duty cleaning (i.e. dishwashing) which comprises the step of treating the articles being cleaned with a composition as disclosed herein.
  • a method of light duty cleaning i.e. dishwashing
  • non-liquid abrasive relates to products in the form of a paste, gel or powder.
  • a particulate abrasive phase is an essential ingredient of compositions according to the present invention.
  • the particulate phase comprises a particulate abrasive which is insoluble in water.
  • the abrasive may be soluble and present in such excess to any water present in the composition that the solubility of the abrasive in the aqueous phase is exceeded and consequently solid abrasive exists in the composition.
  • Suitable abrasives can be selected from, particulate zeolites, calcites, dolomites, feldspar, silicas, silicates, other carbonates, aluminas, bicarbonates, borates, sulphates, and, polymeric materials such as polyethylene.
  • Preferred abrasives for use in general purpose compositions have a Moh hardness of 2-6 although higher hardness abrasives can be employed for specialist applications.
  • Preferred average (weight average) particle sizes for the abrasive fall in the range 0.5-400 microns, with values of around 10-200 microns being preferred. In this range an acceptable compromise between good cleaning behaviour and low substrate damage is achieved.
  • Preferred levels of abrasive range from 60-95wt% on product, preferably in the range 65-90wt%.
  • the physical form of the product will be influenced by the level of abrasive present.
  • compositions with higher levels of abrasive will be powders whereas those with lower levels will be pastes.
  • Exactly where a particular abrasive product changes from powder to paste with a particular abrasive present at decreasing levels is influenced by the other components present. From the preferred embodiments of the invention described below it can be seen that the compositions become a paste if the level of abrasive falls below 80-90%wt.
  • the physical stability of a paste may be improved by having a high level of abrasive present.
  • a high level of abrasive is greater than 80% by weight of the total composition.
  • 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, feldspar and dolomite and mixtures thereof are particularly preferred due to their low cost, suitable hardness and colour.
  • 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 H 2 N-R ⁇ -OH where R ⁇ is a linear or branched alkyl chain having 2-6 carbons.
  • Preferred alkanolamines include:
  • 2-amino-2-methyl-l-propanol mono- di- and tri- ethanolamine, mono-, di- and tri -isopropanolamine, dimethyl-, diethyl or dibutyl ethanolamine, and mixtures thereof.
  • cyclic alkanolamines such as morpholine can also be employed.
  • 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.
  • AMP 2-amino-2-methyl-1- propanol
  • Typical levels of alkanolamine in the compositions of the invention range from l-10%wt. Higher levels are less desirable due to cost and as these may attack certain plastics materials. It is particularly preferred to use 2- amino-2-methyl-l-propanol at a level of 2-6%wt.
  • Suitable electrolyte bases include soluble carbonates and bicarbonates, although the use of hydroxides and other alkaline salts is not excluded. Alkali metal carbonates are particularly preferred, with potassium carbonate being the most preferred. Typical levels of electrolytes range from 0.5-5%wt, with 1- 2.5%wt being particularly preferred.
  • the level of the electrolyte should be such that in use the pH of the composition is raised above the pKa of the alkanolamine, and preferably to a pH at least one unit above the pKa of the alkanolamine. Whether the pH reaches the desired level can be tested by forming a 50%wt slurry of the composition with water and measuring the pH.
  • Electrolyte can serve a further function in compositions which contain relatively low levels of abrasive, in particular when the abrasive level is below 75% on product and/or where the product is in the form of a paste. It is believed that as a abrasive level in the compositions is lowered the compositions become progressively more unstable and the tendency for the compositions to separate into two phases increases. This can be overcome by the use of potassium carbonate as the electrolyte and the addition of water to the composition.
  • compositions which contain potassium carbonate and water it is preferable that the abrasive material is feldspar. It is believed that ion-exchange between the potassium carbonate and the other preferred abrasive materials (particularly dolomite) leads to a progressive buffering of the composition which lowers the pH and eventually reduces the effectiveness of the composition.
  • composition according to the invention will preferably comprise detergent actives which are generally chosen from both anionic and nonionic detergent actives.
  • Surfactant is not a necessary component of the compositions, but provides some foaming which is generally expected by the user and can provide an additional cleaning benefit on certain soils. In some circumstances the presence of surfactant may assist in structuring the product.
  • 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.
  • 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
  • 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.
  • 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
  • the amount of synthetic anionic detergent active to be employed in the detergent composition of this invention will generally be up to 20%, and most preferably from 2 to 15% by weight.
  • Suitable nonionic detergent active compounds can be broadly described as compounds produced by the condensation of alkylene oxide groups, which are hydrophillic in nature, with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature.
  • the length of the hydrophillic 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 hydrophillic 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 R 3 N0, 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 di ethyldodecylamine oxide; tertiary phosphine
  • 10 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 structure R 2 S0 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 15%wt, preferably from 5 to 10% by weight.
  • 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-methyltaurate.
  • 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- (dodecylmethyl sulphonium) propane-1-sulphonate betaine and 3- ( cetyl ethy1phosphonium) ethane sulphonate betaine.
  • detergent-active compounds are compounds commonly used as surface-active agents given in the 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 20%, preferably from 2 to 15% by weight.
  • Solvents other than AMP can be present in the compositions of the invention and their presence is preferred for this reason.
  • Suitable solvents include saturated and unsaturated, linear or branched hydrocarbons, and/or materials of the general formula:
  • R ⁇ and R 2 are independently Cl-7 alkyl or H, but not both hydrogen, m and n are independently 0-5.
  • Preferred solvents are selected from the group comprising C 10 H 16 terpenes, C 10 -C 16 straight chain paraffins, and the glycol ethers.
  • Suitable glycol ethers include di-ethylene glycol mono n- butyl ether, mono-ethylene glycol mono n-butyl ether, propylene glycol n-butyl ether and mixtures thereof.
  • Suitable terpenes include d-limonene.
  • Preferred paraffins include the material available in the marketplace as ' Shellsol-T" [TM] .
  • Typical levels of solvent range from l-15%wt. It is particularly preferred to use terpines at levels l-3%wt. Some of these terpene materials, such as limonene, have the further advantage that the exhibit insect-repellency . We have determined that the terpene materials give better performance at in use 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 in use pH's above 11.
  • glycol ethers are preferred over the other solvents, at typical levels of 5-10%wt on product with di-ethylene glycol mono n-butyl ether being particularly preferred.
  • the ratio of the alkanolamine to the solvent falls in the range 3:1-1:3, with ratios of 1:1 to 1:3 being particularly preferred.
  • a portion of the solvent can be introduced as a perfume component, although the levels of 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.
  • the terpenes are used in this manner as selected terpenes, such as limonene, have a pleasant citrus smell, whereas paraffins and glycol ethers are generally odourless.
  • compositions of the invention can be pastes, gels or powders.
  • Suitable rheological control agents can be present especially when the compositions contain significant amounts of water or low viscosity surfactants. These control agents include fumed silicas and clays .
  • Aerosil 380 (TM) is a suitable structuring agent.
  • compositions which contain mixed surfactant systems are also believed to be stable against phase separation.
  • a composition which contains both an ethoxylated alcohol nonionic surfactant and a nonionic alkyl polyglucoside (APG) surfactant is stable against phase separation.
  • compositions according to the invention may optionally contain polymeric structuring agents to aid in providing appropriate rheological properties 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 CARBOPO , 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.
  • composition of the invention can optionally comprise from 0.1-1% of polymer.
  • composition according to the invention can contain other ingredients which aid in their cleaning performance.
  • 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.
  • 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,
  • R ammo-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.
  • 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) , bactericides, and preservatives (for example 1,2, benzisothiazolin-3-one) .
  • various other optional ingredients such as colourants, whiteners, optical brighteners, soil suspending agents, detersive enzymes, compatible bleaching agents (particularly hypohalites) , bactericides, and preservatives (for example 1,2, benzisothiazolin-3-one) .
  • compositions according to the present invention comprise:
  • l-6%wt preferably 2-6%wt of an alkanolamine selected from the group comprising: 2-amino-2-methyl-l-propanol, mono- di- and tri- ethanolamine, mono, di- and tri- isopropanolamine, dimethyl-, diethyl- or dibutyl- ethanolamine, and mixtures thereof,
  • Imbentin 91 3.5 OFA is a fatty alcohol having an average carbon chain length of C--C 11 and an average degree of ethoxylation at 5 mol EO (ex Libran Chemicals Ltd) .
  • Glucopan 600 CS/UP HH is an alkyl polyglycoside with an average carbon chain length of C 12 -C 14 (ex Henkel) .
  • AMP is 2-amino 2-methyl-l-propanol .
  • Dolomite is a magnesium carbonate/calcium carbonate mix.
  • compositions P1-P3 were prepared as in Table 1 below.
  • Sample preparation entailed pre-mixing the liquid ingredients, then adding the K 2 C0 3 to the dolomite followed by the pre-mixed liquid.
  • Example PI was a powder Pi showed no separation of ingredients.
  • Example P3 was a paste, Example P2 was also a paste.
  • Example 2 use of fumed silica.
  • Example 3 Use water to achieve stability
  • the preferred electrolyte is a soluble carbonate.
  • P2i potassium sulphate
  • P2j potassium iodide
  • Potassium carbonate is a hydratable salt. Potassium sulphate and potassium iodide are non-hydratable. The experiment was repeated replacing the anhydrous potassium carbonate with other anhydrous but hydratable salts, namely sodium carbonate (P2k) and sodium sulphate (P21) . Table 5
  • the sodium carbonate samples with water added showed reduction in the amount of clear layer separation compared to the original sample, but were not as thick as the potassium carbonate.
  • the physical stability of the sodium sulphate sample was not improved by water addition.
  • Example 5 Use of different abrasives
  • Example P2 The pH of 50% slurries of Example P2 and with 2% water was measured initially, and then over a couple of weeks, the slurries being made fresh each time the pH was measured. It was determined that the pH of the water containing samples drops over a couple of weeks.
  • the abrasive of P2 was changed to feldspar (potassium aluminosilicate) .
  • feldspar potassium aluminosilicate
  • 2% water was added to one sample and the pH was monitored as above. Initially the pH of both samples was 11.9. After 10 days the pH of the water free sample was 11.7, whereas the sample with water was 11.8. Thus no pH drop occurred.
  • AOS is Alkyl Olefin Sulphonate
  • LAS is Sodium Alkyl Benzene Sulphonate
  • samples to be tested were diluted to 0.04% active with a 1:4 mixture of Prenton water : demineralised water, giving a final water hardness of ⁇ 5°FH.
  • the diluted samples were thermostatted at 45°C. 100ml of the sample was put in the plunger cylinder, and 0.2ml aliquots of the standard soil added until the foam died. The number of aliquots required to just N kill' the foam was determined. Each sample was tested four times, and the mean and standard deviation calculated.

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Abstract

L'invention concerne une composition de nettoyage abrasive et non liquide comprenant: a) 50 à 99,5 % en poids d'un ou de plusieurs abrasifs particulaires, b) 0,5 à 15 % en poids d'une alcanolamine C2-C6, c) au moins 0,1 % en poids d'une base électrolyte différente d'une alcanolamine, d) éventuellement 0,1 à 20 % en poids d'un ou plusieurs tensioactifs, et e) éventuellement 0,1 à 20 % en poids d'un solvant autre que de l'eau.
PCT/EP1998/002986 1997-06-17 1998-05-11 Composition de nettoyage abrasive WO1998058045A1 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP50364199A JP2002510346A (ja) 1997-06-17 1998-05-11 研磨洗浄組成物
IL13356798A IL133567A0 (en) 1997-06-17 1998-05-11 Abrasive cleaning composition
PL98337460A PL337460A1 (en) 1997-06-17 1998-05-11 Abrasive cleaning composition
SK1790-99A SK179099A3 (en) 1997-06-17 1998-05-11 Abrasive cleaning composition
CA002294204A CA2294204A1 (fr) 1997-06-17 1998-05-11 Composition de nettoyage abrasive
BR9810178-1A BR9810178A (pt) 1997-06-17 1998-05-11 Composição de limpeza não-lìquida abrasiva, e, processo para limpeza de serviço leve
AU80194/98A AU8019498A (en) 1997-06-17 1998-05-11 Abrasive cleaning composition
EP98928304A EP0991744A1 (fr) 1997-06-17 1998-05-11 Composition de nettoyage abrasive

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9712774.0 1997-06-17
GBGB9712774.0A GB9712774D0 (en) 1997-06-17 1997-06-17 Abrasive cleaning composition

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WO1998058045A1 true WO1998058045A1 (fr) 1998-12-23

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EP (1) EP0991744A1 (fr)
JP (1) JP2002510346A (fr)
KR (1) KR20010013911A (fr)
CN (1) CN1267325A (fr)
AU (1) AU8019498A (fr)
BR (1) BR9810178A (fr)
CA (1) CA2294204A1 (fr)
GB (1) GB9712774D0 (fr)
HU (1) HUP0002981A3 (fr)
ID (1) ID24132A (fr)
IL (1) IL133567A0 (fr)
IN (1) IN190659B (fr)
PL (1) PL337460A1 (fr)
SK (1) SK179099A3 (fr)
TR (1) TR200000112T2 (fr)
TW (1) TW440608B (fr)
WO (1) WO1998058045A1 (fr)
ZA (1) ZA984686B (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000020544A1 (fr) * 1998-10-06 2000-04-13 Unilever Plc Composition abrasive non liquide
WO2021041894A1 (fr) * 2019-08-28 2021-03-04 ZestBio, Inc. Composition pour la séquestration de métal à base de galactarate
US11851632B2 (en) 2020-05-14 2023-12-26 Reckitt Benckiser Finish B.V. Solid composition comprising an ethoxylated alcohol with from 30 to 40 ethoxy groups

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101255381B (zh) * 2007-02-27 2012-03-21 3M创新有限公司 清洁方法和组合物
CN102021089A (zh) * 2010-04-19 2011-04-20 铜陵洁雅生物科技股份有限公司 水基汽车柏油清洗剂及其制备方法

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SU883169A1 (ru) * 1980-01-04 1981-11-23 Уральский филиал Всесоюзного научно-исследовательского и проектного института химической промышленности Состав дл чистки твердой поверхности "чистота
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Publication number Priority date Publication date Assignee Title
WO2000020544A1 (fr) * 1998-10-06 2000-04-13 Unilever Plc Composition abrasive non liquide
WO2021041894A1 (fr) * 2019-08-28 2021-03-04 ZestBio, Inc. Composition pour la séquestration de métal à base de galactarate
US11560529B2 (en) 2019-08-28 2023-01-24 ZestBio, Inc. Galactarate based metal sequestration composition
US12065626B2 (en) 2019-08-28 2024-08-20 ZestBio, Inc. Galactarate based metal sequestration composition
US11851632B2 (en) 2020-05-14 2023-12-26 Reckitt Benckiser Finish B.V. Solid composition comprising an ethoxylated alcohol with from 30 to 40 ethoxy groups

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EP0991744A1 (fr) 2000-04-12
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SK179099A3 (en) 2000-07-11
HUP0002981A3 (en) 2001-02-28
TR200000112T2 (tr) 2000-05-22
ID24132A (id) 2000-07-06
CA2294204A1 (fr) 1998-12-23
CN1267325A (zh) 2000-09-20
PL337460A1 (en) 2000-08-14
JP2002510346A (ja) 2002-04-02
IL133567A0 (en) 2001-04-30
GB9712774D0 (en) 1997-08-20
IN190659B (fr) 2003-08-16
ZA984686B (en) 1999-12-01
AU8019498A (en) 1999-01-04
TW440608B (en) 2001-06-16
KR20010013911A (ko) 2001-02-26

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