WO2012146464A1 - Composition de traitement de surface dure - Google Patents
Composition de traitement de surface dure Download PDFInfo
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- WO2012146464A1 WO2012146464A1 PCT/EP2012/056036 EP2012056036W WO2012146464A1 WO 2012146464 A1 WO2012146464 A1 WO 2012146464A1 EP 2012056036 W EP2012056036 W EP 2012056036W WO 2012146464 A1 WO2012146464 A1 WO 2012146464A1
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- pac
- surfactant
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Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/045—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on non-ionic surface-active compounds and soap
-
- 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/047—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on cationic surface-active compounds and soap
-
- 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
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
-
- 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
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3753—Polyvinylalcohol; Ethers or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Definitions
- the present invention is in the field of hard surface treatment compositions.
- the invention particularly relates to hard surface treatment compositions that provide easier cleaning upon the subsequent cleaning.
- Hard surfaces in the home or office are usually cleaned using liquid compositions which comprise one or more surfactants and possibly also pH adjusters like citric acid or sodium salts of citrate.
- the cleaning compositions can be applied in diluted (in water) or undiluted form, in a spray, or rubbed using a cloth or any other convenient way.
- the cleaning composition may be rinsed from the surface after the cleaning. It would be advantageous if the hard surface to be cleaned could be treated with a material which would assist in easier removal of soil and/or stains during subsequent cleaning. This is referred to as the next time cleaning benefit.
- Soils on hard surfaces can become more difficult to remove when not cleaned soon after deposition. When not cleaned promptly, soils can become more adherent to surfaces, more viscous and generally tougher, and require more effort to clean. While not being bound by a theory, this more difficult removal of soils can arise from the effects of drying out of soils, from chemical changes in soils, from reactions of soils with environmental agents such as oxygen, etc. Some soils are more susceptible than others to toughening reactions and processes. Soils comprising or containing chemically unsaturated oils and fats can become very tough and difficult to clean over time, especially when exposed to elevated temperatures. Even light can cause such fatty soils to toughen over time.
- WO 02/18531 discloses a method for cleaning hard surfaces, wherein the surface is treated with an antioxidant, followed by allowing the surface to become dirty, and subsequently cleaning the surface.
- the treatment of the surface with the antioxidant prior to the soiling leads to easier removal of the soil during the subsequent cleaning step.
- the antioxidant may be present in a cleaning composition, or in a rinse composition that is applied after the cleaning.
- cleaning compositions comprising antioxidants, preferably at a concentration of 0.1-10 % by weight, are disclosed. Tannic acid was exemplified to be notably efficient.
- WO 2006/108475 A1 discloses a method for removing fatty soil from a hard surface, the process comprising the sequential steps of (a) treating the hard surface with a liquid cleaning composition; (b) allowing the fatty soil to deposit; and (c) cleaning the surface to remove the fatty soil.
- WO 2010/069731 A1 discloses a method and a composition for treating a fabric substrate to render the substrate repellent to various soils and stains and also hydrophobic. There is disclosed a method of treating the substrate by using a composition of soap and a water soluble trivalent or tetravalent metal and which composition has a pH of less than 6 maintained by the addition of a pH modifying agent.
- Self cleaning surfaces are disclosed in WO04037944 A1 , wherein a process and a composition are disclosed for producing surfaces that are self-cleaning by water, and in particular, there is disclosed an aqueous system for forming transparent self-cleaning surfaces.
- an aqueous mixture comprising nano particles having a particle size of less than 300 nanometers and a surface modifier selected from the group consisting of water-soluble hydrophobic surface modifiers and water-dispersible hydrophobic surface modifiers capable of forming a continuous film from an aqueous solution is provided.
- the aqueous mixture is applied to a surface, and a self-cleaning transparent coating is formed on the surface upon water evaporation.
- the aqueous mixture is essentially free of organic solvents other than coalescing solvents.
- the antioxidants as disclosed by the prior art also may suffer from disadvantages. Consumers may regard residues of antioxidants and/or nano particles on the hard surfaces in e.g. kitchen and bathroom to be harmful and undesired.
- Microemulsion based cleaners comprising metal soaps and silicon material are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (e.g. US 5,759,983 and US 5,741 ,760). However, these are disclosed in the art (
- compositions do not provide the required stain repellence due to lack of hydrophobicity of the surface when the composition is applied.
- surfactants render surfaces hydrophilic, which make them more susceptible to aqueous stain deposition, rather than aqueous stain repellence.
- poly aluminium chloride and a soap in combination with a poly vinyl alcohol and non-ionic or cationic surfactant provides both good cleaning and good stain/soil repellence.
- the present invention provides a hard surface treatment composition
- a hard surface treatment composition comprising 0.01-1 %w of poly-aluminium-chloride (PAC), 0.01 -1 %w of soap of C8-C18 fatty acid, 0.05-1 %w of a surfactant selected from non-ionic surfactants or quaternary ammonium cationic surfactants, 0.05-1 %w ofpoly vinyl alcohol(PVA), and 0.1-1 %w of a quaternary silicon oil, wherein the composition has a pH of between 3 and 5, and the ratio of PAC: soap is between 3:2 and 2:3.
- PAC poly-aluminium-chloride
- soap of C8-C18 fatty acid
- PVA quaternary ammonium cationic surfactants
- PVA poly vinyl alcohol
- 0.1-1 %w of a quaternary silicon oil wherein the composition has a pH of between 3 and 5, and the ratio of PAC: soap is between 3:2 and 2:3.
- the invention provides a process for treating a substrate, comprising the steps in sequence of applying the composition according to the invention to a hard surface and leaving the surface to dry wherein the surface is not rinsed between these steps.
- the invention provides a bottled cleaning composition comprising the compositions according to the invention.
- the invention comprises Poly-aluminium-chloride (PAC), soap of C8-C18 fatty acid, a surfactant selected from non-ionic surfactants or quaternary ammonium cationic surfactants, PVA (poly vinyl alcohol) and a poly siloxane.
- PAC Poly-aluminium-chloride
- soap of C8-C18 fatty acid a surfactant selected from non-ionic surfactants or quaternary ammonium cationic surfactants
- PVA poly vinyl alcohol
- the cleaning compositions according to the invention are preferably for neat application.
- the pH is between 3 and 5.
- Poly aluminium chloride is a known polyelectrolyte.
- the aluminium content is typically 12-20%.
- PAC may have small amount of impurities including traces of S0 4 2" , C0 3 2"; N0 3 “ , Br “ , HC0 3 “ , and HS0 4 " ; but such impurities are typically present in a concentration of less than 2%, more preferably less than 1 %, still more preferably less than 0.5% or even less than 0.1 % by weight of the PAC.
- the PAC is present in the composition in a concentration of between 0.01 - 1 % by weight, preferably at least 0.1 %, more preferably at least 0.25%, or even 0.5% by weight. Additionally it is considered in the context of the present invention to have a mixed metal system, comprising the Aluminium (from PAC) and 0.01 to 1 % by weight of a second metal salt.
- Said second metal salt is selected from bivalent and trivalent metal salts, preferably selected from calcium, zinc and Iron (III).
- the ratio of the PAC to the second metal salt is in the range of 9: 1 to 3:2.
- the soap according to the invention is an alkali metal salt of C8-C18 fatty acid.
- fatty acids are saturated fatty acids selected from Laurie acid, Myristic acid, Palmitic acid, Stearic acid, and combinations thereof; and unsaturated fatty acids, such as Myristoleic acid, Palmitoleic acid, Sapienic acid, Oleic acid, Elaidic acid, Vaccenic acid, Linoleic acid, Linoelaidic acid and a-Linolenic acid, and combinations thereof.
- the alkali metals are sodium, potassium, lithium or their mixtures. Salts of combinations of saturated and unsaturated fatty acids are also contemplated.
- Naturally occurring mixtures predominantly comprising of one or more C8-C18 soap, preferably one or more of the fatty acids as listed above are also included in the scope of the invention.
- Examples of such mixtures are salts of coconut fatty acid and palm kernel fatty acid.
- Soap is present in the composition in a concentration of between 0.01 - 1 % by weight, preferably at least 0.1 %, more preferably atleast 0.25%, or even 0.5% by weight.
- the ratio of PAC to soap is between 3:2 and 2:3, preferably between 4:3 and 3:4, or even between 5:4 and 4:5 for the best results.
- Suitable surfactants in the context of the present invention are nonionic surfactants and quaternary ammonium cationic surfactants. A combination of both quaternary cationic surfactant and nonionic surfactant is also contemplated.
- Non-ionic surfactants are also well- known in the art. They normally consist of a water-solubilising polyalkoxylene
- alkylphenols preferably from 12 to 20 carbon atoms
- dialkylphenols in which each alkyl group contains from 6 to 12 carbon atoms
- primary, secondary or tertiary aliphatic alcohols or alkyl-capped derivatives thereof
- monocarboxylic acids having from 10 to about 24 carbon atoms in the alkyl group and polyoxypropylenes.
- Fatty acid mono- and dialkanolamides in which the alkyl group of the fatty acid radical contains from 10 to about 20 carbon atoms and the alkyloyl group having from 1 to 3 carbon atoms are also common.
- polyalkoxylene moiety usually consists of an average of from 2 to 20 groups of ethylene oxide, propylene oxide groups or mixtures thereof.
- the latter class includes those described in European Patent Specification EP-A-0,225,654, especially for use as all or part of the liquid phase.
- ethoxylated non-ionics which are condensation products of fatty alcohols with from 9 to 15 carbon atoms condensed with 3 to 12 moles of ethylene oxide (generally understood to be an average value).
- condensation products of C 9 to Ci 5 alcohols with 3 or 7 moles of ethylene oxide, or mixtures thereof may be used as the sole non-ionic surfactant or in combination with those described in EP-A-0 225 654.
- the cationic surfactant according to the invention is a quaternary ammonium salt surfactant, characterised in that the ammonium salt has the general formula:
- R1 R2R3R4N+ X- wherein R1 to R4 are alkyl or aryl groups, and X " is an inorganic anion.
- At least one, but typically not more than two, of the alkyl or aryl groups R1- R4 is an alkyl group having a C12-C18 alkyl chain length, or an aryl group, while the remaining alkyl groups are C1-C3 alkyl.
- R1 is preferably a C14-C16 straight chain alkyl group, while R2-R4 are preferably methyl groups.
- quaternary ammonium cationic surfactant are benzalkonium chloride (alkyldimethylbenzylammonium chloride) and cetylpyridinium chloride (CPC).
- the surfactant, non-ionic or cationic or mixtures thereof, is present in the composition in a concentration of 0.05 - 1 % by weight.
- concentration is preferably between 0.1 and 0.8%, more preferably not more than 0.5%, or even at most 0.4% by weight.
- Polyvinyl alcohol (PVOH, PVA, or PVAI) is a water-soluble synthetic polymer.
- PVA Polyvinyl alcohol
- PVAI Polyvinyl alcohol
- homopolymers are the most preferred.
- Homopolymers or copolymers of vinyl alcohol preferably have a molecular mass of between 10 3 and 10 7 u (u is atomic mass unit (SI), also known as “amu”, or “Dalton", “D” or “Da”), more preferably from 10 4 to 10 6 u and most preferably from 30,000 to 500,000 u.
- SI atomic mass unit
- the PVA is present in the composition in a concentration of 0.05 - 1 % by weight.
- the ratio of PVA:surfactant is preferably at least 1 : 1 , more preferably between 1 :1 and 15: 1 , still more preferably between 2: 1 and 15:1. In these ratios the PVA polymer is found to improve the cleaning effect of the surfactant, without rendering the surface hydrophilic.
- the composition further comprises a quaternary silicone oil.
- the preferred quaternary silicon oils are poly siloxanes. Typical examples of such preferred polysiloxanes are siloxanes selected from classes A, B and C below: A. Cyclomethicones
- Cyclomethicones are defined by the general formula I below, m is an integer of greater or equal to 3, and R is a straight or branched alkyl, cycloalkyl, polycycloalkyl, heterocycloalkyl, alkaryl, alkoxy, aryl, aralkyl, alkenyl or alkynyl moiety. More preferred are cyclomethicones wherein m is 3, 4 or 5 as shown in Formulae I la, lib and lie. Especially preferred are low viscosity Cyclomethicones, including hexamethylcyclotrisiloxanes; octamethylcyclotetrasiloxanes and
- Dimethicones are defined by the General formula III below
- R or R1 is typically selected from a straight or branched alkyl, cycloalkyi, polycycloalkyi, heterocycloalkyi, alkaryl, alkoxy, aryl, aralkyi, alkenyl or alkynyl moiety, -H, -OH.
- R and R1 may be the same or different.
- a table exemplifying this is given below.
- Silicone elastomers are defined by the General formula IV below
- R or R1 is typically selected from a straight or branched alkyl, cycloalkyl, polycycloalkyi, heterocycloalkyi, alkaryl, alkoxy, aryl, aralkyi, alkenyl or alkynyl moiety, -H, -OH.
- R and R1 may be the same or different.
- the quaternary silicone oil may be present in the compositions in a concentration of less than 1 % by weight.
- the composition preferably comprises less than 0.5% by weight, but preferably more than 0,1 % by weight.
- composition according to the invention may also comprise an abrasive material.
- the abrasive particles are used in an amount of at least 0.1 %, preferably 0.5%. In order to retain the transparent character of the total composition the maximum amount of particles is 20%, preferably 10%, more preferably 5%.
- the particles may be made of abrasive materials known in the art. Thus, they may consist of granules of one or more of the well known inorganic abrasives such as silica, silicates, calcite and the like. They may consist of polymer granules, such as polyethylene, polypropylene, polycarbonate and the like. Particularly suitable are granules of a biodegradable polymer, such as the starch-derived plastics known in the art. Alternatively, the abrasive particles may be made of softer materials such as hard waxes and fats, hard fatty acids, hard fatty acid soaps and the like. Such materials may also be mixed with fine particles of any of the known abrasives or with other materials, preferably solid materials, suitable for improving the cleaning process and thereafter formed into granules of the required size.
- the particles are preferred to be macroscopic, i.e. clearly visible separately to the naked eye. This is in contrast to most abrasive powder particles which generally have average particle size well below 0.3mm and in the vast majority of cases at most 0.1 mm (100 ⁇ ), or even less than 0.05mm, which are also contemplated in the context of the invention for opaque compositions.
- the particles according to the invention have an average particle size between 0.3 and 2.5mm, preferably more than 0.5 and at most 1.5mm, while for opaque compositions a particles size below 0.3 mm is preferred.
- the visual appeal of the compositions is considerably enhanced if the particles are of fairly uniform particle size i.e. they all have a particle size within the range of plus or minus 70% of the average particle size, preferably within a range of plus or minus 50%, more preferably plus or minus 30%.
- the visual appeal of the particles, and therefore the total composition, is further enhanced if the particles have a certain minimum sphericity, such that the ratio between the longest and the shortest diameter of a particle in any one direction is at most 3:1 , preferably at most 2:1 or even 1.5: 1.
- Particularly preferred are particles with a round, preferably a smooth round shape.
- Such particles may be made by prilling processes involving making a melt of the particle material, converting it into droplets, which are thereafter cooled in a gas (air) flow.
- Various processes and suitable equipment therefore are known in the art and may be applied to the organic abrasives, provided they are sufficiently low melting.
- High melting powders such as inorganic abrasive powders may be made into suitably shaped particles by various
- the cleaning compositions according to the invention may consist of a colourless liquid and solid particles having their natural colour (in many cases white), the compositions are considerably more attractive to the consumer if the liquid and the particles have clearly different colours. They may have different shades of the same colour, e.g. dark blue particles in a light blue liquid, or preferably, the liquid and the particles have contrasting colours e.g. white particles in a blue, green or yellow liquid or vice versa, or coloured particles in a differently coloured liquid.
- composition may further comprise perfumes, bleaches, anti bacterial agents, fluoro-polymers and insect repellent materials.
- the perfume may be any commercially available water soluble or miscible perfume composition.
- gloss and cleaning improving aids as known in the are, such as 2-phenoxy ethanol (commercially available as Dowanol ex Dow) may be added in a concentration of 0.05 - 0.5% by weight of the composition,
- the pH of the composition according to the invention is between 3 and 5.
- Aluminum salts form different positively charged hydrated species in water in acidic pH eg: Al 2 (OH) 2 4+ and Al 3 (OH) 4 5+ .
- Polyaluminum chloride may also form Ali3 0 4 (OH) 24 7+ in solution, while the fatty acid has a pK a of 4.5, yielding a pH range of 3-5 in the mixture. This is thought to cause the precipitation of the hydrophobic compound onto the surface.
- composition is preferably an aqueous liquid, however the formulations made in mixed solvents comprising alcohols, including methanol, ethanol and/or isopropanol, where the water to solvent ratio is 20:1 to 99: 1 are also contemplated.
- alcohols including methanol, ethanol and/or isopropanol, where the water to solvent ratio is 20:1 to 99: 1 are also contemplated.
- the invention provides a process for treating a substrate, comprising the steps in sequence of applying the composition according to the invention to a hard surface and leaving the surface to dry wherein the surface is not rinsed between these steps.
- the surface is subject to the deposition of dirt after treatment.
- the surface is found to be more repellent to aqueous stains when treated with the composition of the invention.
- the surface may be cleaned again with the treatment composition according to the invention or another composition, preferably with the treatment composition according to the invention.
- composition may be packaged in the form of any commercially available liquid composition, typically in the form of a bottle containing the liquid.
- the composition is preferably applied using a trigger spray applicator.
- a trigger spray application enables fast and easy use for the consumer and additionally it brings a suitable amount of air into the composition, which aides in the foam formation.
- compositions of the invention may be stored in and dispensed by any suitable means, but spray applicators are particularly preferred. Pump dispensers (whether spray or non-spray pumps) are also possible.
- the present invention provides a container for a liquid hard surface cleaner, the container comprising a reservoir containing the hard surface cleaning composition of the invention, and spray dispenser for dispensing the composition in the form of a spray.
- the spray dispenser is preferably a trigger spray but may be any mechanical means for ejecting the liquid in spray or aerosol form.
- DCFA Na-salt of distilled coco-fatty acid, ex Godrej Industries Ltd, India
- CPC Cetylpyridinium chloride
- the contact angle of the sessile droplet was measured using a Kruss goniometer by placing a 10 microlitre of distilled water droplet on the glass slide. The angle was analyzed by the image J software using the Drop snake plug-in.
- Example 1 Effect on contact angle and oily soil cleaning of glass slides.
- Example 2 Effect of the type of nonionic EO on the stain repellence and cleaning:
- the type of EO does not have any effect on the performance, while the table above indicates that different concentrations of PAC and Soap varies the performance on stain repellence (contact angle).
- Example 3 Effect of the amount of nonionic EO on stain repellence and cleaning
- the amount of nonionic should be more than 0.05% in examples Ex5-Ex8 compared to comparative example J.
- Nonionic surfactant variation shows that the the best cleaning is obtained at at least 0.05% surfactant, while the best stain repellence is obtained between 0.05 - 0.5% surfactant, although acceptable results are still obtained at higher surfactant concentrations.
- nonionic (ex 9) and cationic (Ex 10) are compared to anionic surfactant (comparative M).
- Example 5 Effect of pH of the treatment formulation on stain repellence and cleaning:
- compositions with in the pH range according to the invention (Ex 10 and 11), compared to comparative examples N, O and P, outside the claimed range.
- Stain repellence decreases at high pH and so the preferred pH is ⁇ 6.
- Example 6 Effect of PVA and EO combination on stain repellence and cleaning In this example different ratios of surfactant and PVA are compared.
- Example 9 mixed metal example (Calcium)
- compositions are given below. All composition contained 0.55% PVA, 0.1 % PDMS, 0.1 % of abrasive particles, and 0.25% Nonionic (1 : 1 ⁇ 03 ⁇ 07)
- compositions are given below. All composition contained 0.55% PVA, 0.1 % PDMS, 0.1 % of abrasive particles, and 0.25% Nonionic (1 : 1 ⁇ 03 ⁇ 07)
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Abstract
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP20120711656 EP2702129B1 (fr) | 2011-04-25 | 2012-04-03 | Composition de traitement de surface dure |
CN201280020247.9A CN103492544B (zh) | 2011-04-25 | 2012-04-03 | 硬质表面处理组合物 |
PL12711656T PL2702129T3 (pl) | 2011-04-25 | 2012-04-03 | Kompozycja do traktowania twardych powierzchni |
BR112013027410A BR112013027410A2 (pt) | 2011-04-25 | 2012-04-03 | composição de tratamento de superfícies duras, processo de tratamento de substratos, composição de limpeza engarrafada e garrafa |
EA201301192A EA024738B1 (ru) | 2011-04-25 | 2012-04-03 | Композиция для обработки твердой поверхности и способ ее использования |
ES12711656.4T ES2535020T3 (es) | 2011-04-25 | 2012-04-03 | Composición para el tratamiento de superficies duras |
ZA2013/07836A ZA201307836B (en) | 2011-04-25 | 2013-10-21 | Hard surface treatment composition |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1293MU2011 | 2011-04-25 | ||
IN1293/MUM/2011 | 2011-04-25 | ||
EP11170338.5 | 2011-06-17 | ||
EP11170338 | 2011-06-17 | ||
IN3274/MUM/2011 | 2011-11-22 | ||
IN3274MU2011 | 2011-11-22 |
Publications (1)
Publication Number | Publication Date |
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WO2012146464A1 true WO2012146464A1 (fr) | 2012-11-01 |
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ID=45926577
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP2012/056036 WO2012146464A1 (fr) | 2011-04-25 | 2012-04-03 | Composition de traitement de surface dure |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP2702129B1 (fr) |
CN (1) | CN103492544B (fr) |
AR (1) | AR086479A1 (fr) |
EA (1) | EA024738B1 (fr) |
ES (1) | ES2535020T3 (fr) |
PL (1) | PL2702129T3 (fr) |
WO (1) | WO2012146464A1 (fr) |
ZA (1) | ZA201307836B (fr) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0225654A1 (fr) | 1985-11-11 | 1987-06-16 | Unilever N.V. | Composition détergente liquide non aqueuse à adjuvant actif |
US5741760A (en) | 1993-08-04 | 1998-04-21 | Colgate-Palmolive Company | Aqueous cleaning composition which may be in microemulsion form comprising polyalkylene oxide-polydimethyl siloxane |
US5759983A (en) | 1993-08-04 | 1998-06-02 | Colgate-Palmolive Co. | Aqueous cleaning composition which may be in microemulsion form comprising polyalkylene oxide -polydimethyl siloxane and ethoxylated secondary alcohol |
WO2002018531A1 (fr) | 2000-08-29 | 2002-03-07 | Unilever N.V. | Assistance au nettoyage |
WO2004037944A1 (fr) | 2002-10-23 | 2004-05-06 | S. C. Johnson & Son, Inc. | Procede et composition permettant de produire des surfaces autonettoyantes a partir de systemes aqueux |
WO2006083813A2 (fr) * | 2005-01-31 | 2006-08-10 | The Procter & Gamble Company | Composition d'agent de rinçage |
WO2006108475A1 (fr) | 2005-04-13 | 2006-10-19 | Unilever N.V. | Composition de nettoyage liquide destinee a une surface dure |
WO2010069731A1 (fr) | 2008-12-16 | 2010-06-24 | Unilever Nv | Procédé et composition pour le traitement d'un substrat |
-
2012
- 2012-04-03 ES ES12711656.4T patent/ES2535020T3/es active Active
- 2012-04-03 CN CN201280020247.9A patent/CN103492544B/zh not_active Expired - Fee Related
- 2012-04-03 EA EA201301192A patent/EA024738B1/ru not_active IP Right Cessation
- 2012-04-03 PL PL12711656T patent/PL2702129T3/pl unknown
- 2012-04-03 EP EP20120711656 patent/EP2702129B1/fr not_active Not-in-force
- 2012-04-03 WO PCT/EP2012/056036 patent/WO2012146464A1/fr active Application Filing
- 2012-04-23 AR ARP120101387 patent/AR086479A1/es unknown
-
2013
- 2013-10-21 ZA ZA2013/07836A patent/ZA201307836B/en unknown
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0225654A1 (fr) | 1985-11-11 | 1987-06-16 | Unilever N.V. | Composition détergente liquide non aqueuse à adjuvant actif |
US5741760A (en) | 1993-08-04 | 1998-04-21 | Colgate-Palmolive Company | Aqueous cleaning composition which may be in microemulsion form comprising polyalkylene oxide-polydimethyl siloxane |
US5759983A (en) | 1993-08-04 | 1998-06-02 | Colgate-Palmolive Co. | Aqueous cleaning composition which may be in microemulsion form comprising polyalkylene oxide -polydimethyl siloxane and ethoxylated secondary alcohol |
WO2002018531A1 (fr) | 2000-08-29 | 2002-03-07 | Unilever N.V. | Assistance au nettoyage |
WO2004037944A1 (fr) | 2002-10-23 | 2004-05-06 | S. C. Johnson & Son, Inc. | Procede et composition permettant de produire des surfaces autonettoyantes a partir de systemes aqueux |
WO2006083813A2 (fr) * | 2005-01-31 | 2006-08-10 | The Procter & Gamble Company | Composition d'agent de rinçage |
WO2006108475A1 (fr) | 2005-04-13 | 2006-10-19 | Unilever N.V. | Composition de nettoyage liquide destinee a une surface dure |
WO2010069731A1 (fr) | 2008-12-16 | 2010-06-24 | Unilever Nv | Procédé et composition pour le traitement d'un substrat |
Non-Patent Citations (4)
Title |
---|
"McCutcheon's Emulsifiers and Detergents", MANUFACTURING CONFECTIONERS COMPANY |
H. STACHE: "Tenside-Taschenbuch", 1981, CARL HAUSER VERLAG |
SCHWARTZ; PERRY: "Surface Active Agents", vol. 1, 1949, INTERSCIENCE |
SCHWARTZ; PERRY; BERCH: "SURFACE ACTIVE AGENTS", vol. 2, 1958, INTERSCIENCE |
Also Published As
Publication number | Publication date |
---|---|
EP2702129B1 (fr) | 2015-01-07 |
ZA201307836B (en) | 2015-01-28 |
PL2702129T3 (pl) | 2015-06-30 |
CN103492544B (zh) | 2015-05-27 |
CN103492544A (zh) | 2014-01-01 |
EA201301192A1 (ru) | 2014-06-30 |
AR086479A1 (es) | 2013-12-18 |
EP2702129A1 (fr) | 2014-03-05 |
ES2535020T3 (es) | 2015-05-04 |
EA024738B1 (ru) | 2016-10-31 |
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