The invention relates to home care formulations comprising a dicarboxy functionalized polyorganosiloxane; they can be used for the treatment of hard surfaces, as well as textile article surfaces.
Organofunctional silicones are well-known in the art. The siloxane units may be functionalized with substituents such as carboxyalkyl (EP-A-196 169; U.S. Pat. No. 5,702,490), carboxyalkylaminoalkyl (U.S. Pat. No. 5,516,869), carboxyetheralkyl (U.S. Pat. No. 4,658,049), with radicals derived from alkenyl succinic anhydride (U.S. Pat. No. 4,876,152) optionally amidated (U.S. Pat. No. 6,007,801) and can be used for the treatment of surfaces in various type of industries, such as metal, leather, personal care, plastics, masonry
It has now been found that dicarboxy functionalized polyorganosiloxanes can be used in home care formulations, particularly in cleaning, rinsing or care compositions for the treatment of industrial, domestic or communal hard surfaces, as well as textile article surfaces, targeted at conferring on the above surfaces benefits such as water repellency, soil release, stain resistance, anti-fogging, surface repair, anti-wrinkling, shine, lubrication and/or at improving the residuality, impact and or efficacy of active materials comprised in said compositions on the surfaces treated therewith.
While the specification concludes with claims, which particularly point out and distinctly claim the invention, it is believed the present invention will be better understood from the following description.
All percentages and ratios used herein are by weight of the total composition unless otherwise specified. All measurements are made at 25° C., unless otherwise specified.
Herein, “comprising” means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the terms “consisting of” and “consisting essentially of”.
The home care formulation according to the invention comprises at least one dicarboxy functionalized polyorganosiloxane having the formula (I)
X(R4R5 Si O)p(R6 A Si O)q Y (I)
wherein
The ratio of the number of Z and W end groups to the total number of end groups X and Y ranges from 0/100 to 75/100, preferably from 0/100 to 30/100. The products where Z is —OH and/or Y is —H, are by-products.
The salts of the dicarboxy radical can be alkali metal (sodium, potassium, lithium) salts, alkaline earth metal (calcium, barium) salts, non substituted or substituted ammonium (methyl-, dimethyl-, trimethyl-, or tetramethylammonium, dimethylpiperidinium) salts or can derive from an alkanolamine (monoethanolamine, diethanolamine, triethanolamine).
In a preferred embodiment, the p/q ratio is from 1/3 to 99/1 (corresponding to 1-75% of pendant diacid groups relative to the siloxyl units), preferably from 1/1 to 10/1.
In addition to the mono- or diester derivatives of the dicarboxy radical, (M=alkyl), the present invention includes the amide and diamide derivatives.
The present dicarboxy functionalized siloxane polymers are generally prepared by a hydrosilylation reaction of a polyalkylhydrogensiloxane and an alpha-olefinic anhydride, the precursor of the dicarboxy A groups, with the aid of an effective amount of a hydrosilylation metal catalyst (platinum), as described for example, in U.S. Pat. Nos. 3,159,601; 3,159,662; and 3,814,730, followed by hydrolysis of the anhydride groups.
The hydrosilylation reaction can be carried out at a temperature from 20 to 200° C., preferably from 60 to 120° C., preferably with the aid of a platinum KARSTEDT catalyst (from 1 to 300 ppm, preferably from 5 to 50 ppm by weight of Pt). The relative quantities of polyalkylhydrogensiloxane and alpha alkenyl anhydride corresponds to a stoichiometric excess of alpha alkenyl anhydride (at most 5 moles of alpha alkenyl anhydride per mole of polyalkylhydrogensiloxane, preferably at most 2 moles of alpha alkenyl anhydride per mole of polyalkylhydrogensiloxane.
The hydrolysis reaction can be carried out with water at a temperature ranging from room temperature to 150° C., preferably from 40 to 120° C., with or without catalysts. Suitable catalysts for the reaction can be Lewis acids such as TiCl4, ZnCl2, MgCl2, or Bronstedt acids or bases such as CH3COOH, H2SO4, HCl, KOH, NaHCO3, in an amount ranging from 0.05 to 5%.
Preferred polymers comprise one or a combination of the following dicarboxy acid pendant groups:
—(CH2)n—CH(COOM)2
—(CH2)n—CH(COOM)—CH2COOM
In a preferred embodiment, the diacid pendant group A in the functionalized polyorganosiloxane is —(CH2)3—CH(COOM)—CH2COOM, the polymer prepared by a hydrosilylation reaction of a polyalkylhydrogensiloxane and allyl succinic anhydride followed by hydrolysis of the anhydride groups. Preferably, the polyalkylhydrogensiloxane is polydimethylhydrogensiloxane and the polymer is terminated with trimethylsilyl groups.
Said home care formulations can be used particularly for cleaning, rinsing, care or treatment of industrial, domestic or communal hard surfaces, as well as textile article surfaces; they are targeted at conferring on the latter benefits such as water repellency, soil release, stain resistance, anti-fogging, surface repair, anti-wrinkling, shine, lubrication and/or at improving the residuality, impact and or efficacy of active materials comprised in said compositions on the surfaces treated therewith.
The term “hard surfaces” more particularly means surfaces such as glass, windowpanes, ceramic, tiling, walls, floors, dishwares, stainless steel, hard organic polymer, wood; most particularly it means inorganic surfaces.
The dicarboxy functionalized polyorganosiloxane of formula (I) can be present in said formulations at a concentration of from about 0.005% to 10% by weight, preferably from about 0.05% to 5% by weight.
The home care formulation according to the invention can be applied to the surface to be treated in an amount such that it allows, after rinsing if necessary, and after drying, a deposit of dicarboxy functionalized polyorganosiloxane of from 0.0001 to 10 g/m2, preferably from 0.001 to 1 g/m2, of surface to be treated.
The home care formulation according to the invention preferably comprises at least one surfactant and/or at least one additive or active component.
Except when otherwise indicated, the proportions are shown in % by weight (in dry matter) based on the total weight of the home care formulation.
The surfactant is advantageously anionic and/or nonionic. It can also be cationic, amphoteric or zwitterionic.
Among the anionic surfactants which may be mentioned in particular are soaps such as salts of C8-C24 fatty acids, for example the salts of fatty acids derived from copra and from tallow; alkylbenzenesulphonates, in particular alkyl-benzenesulphonates of linear C8-C,3 alkyl, in which the alkyl group comprises from 10 to 16 carbon atoms, alcohol-sulphates, ethoxylated alcohol-sulphates, hydroxyalkyl sulphonates; alkylsulphates and sulphonates, in particular of C12-C16, monoglyceride sulphates and condensates of fatty acid chlorides with hydroxyalkyl sulphonates.
Advantageous anionic surfactants are, in particular:
Additional examples of suitable surfactants are compounds generally used as surfactants denoted in the renowned texts Surface Active Agents, volume I by Schwartz and Perry, and Surface Active Agents and Detergents, volume II by Schwartz, Perry and Berch. The surfactants can be present in a proportion of from about 0.005% to about 60% by weight, in particular from about 0.5% to about 40% by weight, more preferably from about 0.1% to about 25% by weight, depending on the nature of the surfactant(s) and the destination of the home care formulation.
Mention may be made, among the other common additives and/or active agents which are part of the formulation of cleaning, rinsing or care compositions, of:
The composition of the invention is particularly suitable for cleaning ceramic surfaces (floor tiles, baths, sinks, etc.).
The cleaning formulation advantageously comprises from about 0.02% to about 5% by weight of dicarboxy functionalized polyorganosiloxane of formula (I) relative to the total weight of said formulation, as well as at least one surfactant, preferably a nonionic surfactant. The amount of nonionic surfactants is generally from 0 to about 30% by, weight, preferably from 0 to about 20% by weight. An anionic surfactant can optionally be present in an amount of from 0 to about 30% by weight, advantageously from 0 to about 20% by weight. The total amount of surfactants used in this type of composition is generally between about 1.5% and about 50% by weight, preferably between about 5% and about 30% by weight and more particularly between about 10% and about 20% by weight.
The formulation can also contain organic or inorganic detergent adjuvants (“builders”) as mentioned above; in general, the detergent adjuvant is used in an amount of between about 0.1 and about 25% by weight.
In addition to the ingredients mentioned above, the formulation can also contain other optional ingredients such as pH modifiers, foam modifiers (soaps), dyes, optical brighteners, soiling-suspension agents, detergent enzymes, compatible bleaching agents, agents for controlling gel formation, freezing-thawing stabilizers, bactericides, preserving agents, solvents, fungicides, insect repellents, hydrotropic agents, fragrances, opacifiers or pearlescent agents.
The pH of the composition is advantageously between about 3 and about 11.
The composition of the invention can also be used for cleaning toilet bowls. The cleaning formulation advantageously comprises from about 0.05% to about 5% by weight of dicarboxy functionalized polyorganosiloxane of formula (I) relative to the total weight of said formulation. The composition for cleaning toilet bowls also comprises from about 0.5% to about 10% by weight of a surfactant so as to contribute towards removing soiling or so as to give foaming or wetting properties, or alternatively in order to increase the cleaning efficacy of the composition. The surfactant is preferably an anionic or nonionic surfactant. Cationic surfactants can also be added in order to provide germicidal properties.
The composition for cleaning toilet bowls can also comprise an acidic cleaning agent which can consist of an inorganic acid such as phosphoric acid, sulphamic acid, hydrochloric acid, hydrofluoric acid, sulphuric acid, nitric acid or chromic acid and mixtures thereof or an organic acid, in particular acetic acid, hydroxyacetic acid, adipic acid, citric acid, formic acid, fumaric acid, gluconic acid, glutaric acid, glycolic acid, malic acid, maleic acid, lactic acid, malonic acid, oxalic acid, succinic acid or tartaric acid and mixtures thereof, acid salts such as sodium bisulphate, and mixtures thereof. The amount of acid ingredients is preferably between about 0.1% and about 40% by weight, and preferably between about 0.5% and about 15% by weight.
The composition for cleaning toilet bowls can also comprise a thickener such as a gum, in particular a xanthan gum, added at a concentration of from about 0.1% to about 3%, as well as one or more of the following minor ingredients (a preserving agent intended to prevent the growth of microorganisms in the product, a dye, a fragrance and/or an abrasive agent).
The pH of the composition is from about 0.5 to about 12.
The composition according to the invention is also suitable for rinsing shower walls.
The rinsing formulation advantageously comprises from about 0.02% to about 5% by weight of dicarboxy functionalized polyorganosiloxane of formula (I) relative to the total weight of said formulation. The other main active components of the aqueous compositions for rinsing showers are at least one surfactant (polyethoxylated fatty esters, alkylpolyglucosides) present in an amount ranging from about 0.5 to about 5% by weight and optionally a metal-chelating agent present in an amount ranging from about 0.01 to about 5% by weight. The preferred metal-chelating agents are ethylenediaminetetraacetic acid (EDTA) and analogues thereof.
The aqueous compositions for rinsing showers advantageously contain water with, optionally, at least one lower alcohol in major proportion and additives in minor proportion (between about 0.1% and about 5% by weight, more advantageously between about 0.5% and about 3% by weight and even more preferably between about 1% and about 2% by weight).
The pH of the composition is advantageously between about 7 and about 11.
The composition according to the invention can also be used for cleaning glass-ceramic plates.
The formulation for cleaning glass-ceramic plates advantageously comprises from about 0.1% to about 5% by weight of dicarboxy functionalized polyorganosiloxane of formula (I) relative to the total weight of said formulation. Advantageously, the formulations for cleaning glass-ceramic plates comprise a thickener such as a xanthan gum (from about 0.1 to about 1%), an abrasive agent such as calcium carbonate or silica (from about 10% to about 40%), a glycol such as butyldiglycol (from 0 to about 7%), a nonionic surfactant (from about 1% to about 10%) and optionally basifying agents or sequestering agents.
The pH of the composition is advantageously between about 7 and about 12.
The composition of the invention is also advantageous for cleaning dishes by hand or in an automatic device.
The formulation for hand cleaning dishes advantageously comprises from about 0.05% to about 5% by weight of dicarboxy functionalized polyorganosiloxane of formula (I) relative to the total weight of said formulation.
In the case of cleaning dishes in an automatic device, said dicarboxy functionalized silicone can be present either in the detergent formula used in the washing cycle or in the rinsing liquid.
The cleaning formulation for autodishwashers also comprise:
The pH of the formulation is advantageously between about 8 and about 12.
Formulations for rinsing dishes in an automatic dishwasher advantageously also comprise from about 0.2 to about 20%, preferably from about 0.5 to about 15%, of a surfactant, preferably a nonionic surfactant or a mixture of nonionic and anionic surfactant.They also comprise from 0 to about 10%, preferably from about 0.5 to about 5% of a calcium-sequestering organic acid, preferably citric acid. They can also comprise an auxiliary agent of copolymer of acrylic acid and of maleic anhydride or acrylic acid homopolymers type, in an amount of from 0 to about 15%, preferably from 0.5 to about 10%.
The pH of the formulation is advantageously between about 4 and about 7.
The composition of the invention is also advantageous for washing up dishes by hand.
Preferred liquid detergent formulations of this type also comprise from about 3 to about 50, preferably from about 10 to about 40, parts by weight of at least one surfactant, preferably an anionic surfactant, chosen in particular from sulfates of saturated C5-C24, preferably C10-C16, aliphatic alcohols, optionally condensed with approximately from about 0.5 to about 30, preferably from about 0.5 to about 5, particularly from about 0.5 to about 3, mol of ethylene oxide, in acid form or in the form of a salt, nonionic surfactants, such as amine oxides, alkylglucamides, oxyalkylenated fatty alcohol derivatives, alkylamides or alkanolamides, amphoteric surfactants or zwitterionic surfactants, bactericides or disinfectants, such as triclosan, synthetic cationic polymers, polymers for controlling the viscosity of the mixture and/or the stability of the foams formed during use, hydrotropic agents, hydrating or moisturizing agents or agents for protecting the skin, dyes, fragrances, preservatives, and the like.
The pH of the formulation is advantageously between about 6 and about 8.
The formulation of the invention can also be used for the treatment of glass surfaces, in particular window panes.
The formulation for cleaning window panes comprises:
The formulations for cleaning window panes can also contain:
The pH of the composition is advantageously between about 6 and about 11.
The composition of the invention can also be used for the external cleaning of motor vehicles, more particularly, the bodywork thereof. In this case also, the dicarboxy functionalized silicone according to the invention can be present either in a detergent formula used for the washing operation or in a rinsing product.
The formulation for external cleaning of of motor vehicles comprises from about 0.05% to about 5% by weight of at least one dicarboxy functionalized polyorganosiloxane of formula (I). The cleaning composition for motor vehicles advantageously comprises nonionic surfactants (in an amount of from 0 to about 30%, preferably from of about 0.5 to about 15%), amphoteric and/or zwitterionic surfactants (in an amount of from 0 to about 30%, preferably from of about 0.5 to about 15%), cationic surfactants (in an amount of from 0 to about 30%, preferably from about 0.5 to about 15%), anionic surfactants (in an amount of from 0 to about 30%, preferably from about 0.5 to about 15%), organic or inorganic detergency adjuvants (builders), hydrotropic agents, fillers, pH modifiers, and the like. The minimum amount of surfactant present in this type of composition is at least about 1% of the formulation.
The pH is avantageously between about 8 and about 12.
The composition of the invention can also be used for washing laundry, particularly polyamide, silk, cotton or wool fabrics.
The formulation for washing laundry comprises from about 0.01% to about 3% by weight of at least one dicarboxy functionalized polyorganosiloxane of formula (I). The other active component of the composition for washing laundry is at least one surfactant (in an amount of from about 5 to about 70%, preferably from about 5 to about 50%); said composition can also comprise at least an inorganic or organic detergent adjuvant (builder in an amount of from about 5 to about 50%), chelating agents, enzymes (proteases, amylases, lipases, peroxidases, up to about 5 mg by weight of active enzyme/g of composition), softeners such as clay (about 0.5- about 10%), fragrance, foam suppressants (up to about 5%), soil release polymers such as cellulose derivatives, ethyleneglycol terephthalate/polyethylene glycol copolymers, ethyleneglycol terephthalate/polyethylene glycol/polyisophthalate copolymers (about 0.01- about 10%), anti-redeposition agents such as carboxymethylcellulose (about 0.01- about 10%), anti-color transfert polymers such as polyvinylpyrrolidones (about 0.05- about 5%).
Another subject-matter of the invention is an aqueous biocidal home care formulation which contains
If desired, a solubilizing agent can be present in said composition in order to facilitate the solubilization of said biocide. As examples of solubilizing agents, mention may be made of alcohols such as ethanol, isopropanol, propylene glycol or other solvents. Said formulation can be a detergent composition, in particular for washing up dishes by hand, for cleaning and disinfecting hard industrial, domestic or community surfaces.
The aqueous biocidal formulation may also comprise additives such as chelating agents [such as aminocarboxylates (ethylenediaminetetraacetates, nitrilotriacetates, N,N-bis(carboxymethyl)glutamates, citrates)], alcohols (ethanol, isopropanol, glycols), detergent adjuvants (phosphates, silicates), surfactants, dyes, fragrances or the like.
Compositions for washing up dishes by hand can also contain surfactants, viscosity-modifying agents, hydrotropic agents, fragrances, dyes or the like.
The cleaning or disinfection operation consists in applying or placing said aqueous biocidal formulation, optionally diluted from about 1 to about 1000 times, preferably from about 1 to about 100 times, in contact with the surface to be treated.
The amount of aqueous biocidal formulation which can favourably be used is that corresponding to a deposition of from about 0.01 to about 10 g, preferably from about 0.1 to about 1 g, of biocide per m2 of surface and to a deposition of from about 0.001 to about 2 g, preferably from about 0.01 to about 0.5 g, of dicarboxy functionalized silicone per m2 of surface.
Among the microorganisms whose proliferation can be controlled using the biocidal formulation of the invention, mention may be made of
Further, the present aqueous biocidal compositions can be incorporated into an insoluble substrate for application to a surface such as in the form of a treated wipe. Suitable water insoluble substrate materials and methods of manufacture are described in Riedel, “Nonwoven Bonding Methods and Materials,” Nonwoven World (1987); The Encyclopedia Americana, vol. 11, pp. 147-153, vol. 21, pp. 376-383, and vol. 26, pp. 566-581 (1984); U.S. Pat. No. 3,485,786 to Evans, issued Dec. 23, 1969; U.S. Pat. No. 2,862,251, to Kalwarres; U.S. Pat. No. 3,025,585, Kalwarres; U.S. Pat. No. 4,891,227, to Thaman et al., issued Jan. 2, 1990; and U.S. Pat. No. 4,891,228 and U.S. Pat. No. 5,686,088 to Mitra et al., issued Nov. 11, 1997; U.S. Pat. No. 5,674,591; James et al; issued Oct. 7, 1997.
Nonwoven substrates made from synthetic materials useful in the present invention can also be obtained from a wide variety of commercial sources. Nonlimiting examples of suitable nonwoven layer materials useful herein include PGI Miratec Herringbone, a patterned hydroentangled material containing about 30% rayon and 70% polyester, and having a basis weight of about 56 grams per square yard (gsy), available from PGI/Chicopee, Dayton N.J.; PGI Miratec Starburst, a patterned hydroentangled material containing about 30% rayon and 70% polyester, and having a basis weight of about 56 grams per square yard (gsy), available from PGI/Chicopee, Dayton N.J.; NovonetR 149-616, a thermo-bonded grid patterned material containing about 100% polypropylene, and having a basis weight of about 50 gsy, available from Veratec, Inc., Walpole, Mass.;
NovonetR 149-801, a thermo-bonded grid patterned material containing about 69% rayon, about 25% polypropylene, and about 6% cotton, and having a basis weight of about 75 gsy, available from Veratec, Inc. Walpole, Mass.; NovonetR 149-191, a thermo-bonded grid patterned material containing about 69% rayon, about 25% polypropylene, and about 6% cotton, and having a basis weight of about 100 gsy, available from Veratec, Inc. Walpole, Mass.; HEF NubtexR 149-801, a nubbed, apertured hydroentangled material, containing about 100% polyester, and having a basis weight of about 70 gsy, available from Veratec, Inc. Walpole, Mass.; KeybakR 951V, a dry formed apertured material, containing about 75% rayon, about 25% acrylic fibers, and having a basis weight of about 43 gsy, available from PGI/Chicopee, Dayton, N.J.; KeybakR 1368, an apertured material, containing about 75% rayon, about 25% polyester, and having a basis weight of about 39 gsy, available from PGI/Chicopee, Dayton, N.J.; DuralaceR 1236, an apertured, hydroentangled material, containing about 100% rayon, and having a basis weight from about 40 gsy to about 115 gsy, available from PGI/Chicopee, Dayton, N.J.; DuralaceR 5904, an apertured, hydroentangled material, containing about 100% polyester, and having a basis weight from about 40 gsy to about 115 gsy, available from PGI/Chicopee, Dayton, N.J.; Sontara 8877, an apertured hydroentangled material, containing about 50% Nylon and about 50% Pulp, and having a basis weight of about 68 gsm, available from Dupont Chemical Corp. Alternatively, the water insoluble substrate can be a polymeric mesh sponge as described in U.S. Pat. No. 5,650,384. The polymeric sponge comprises a plurality of plies of an extruded tubular netting mesh prepared from a strong flexible polymer, such as addition polymers of olefin monomers and polyamides of polycarboxylic acids. Although these polymeric sponges are designed to be used in conjunction with a liquid cleanser, these types of sponges can be used as the water insoluble substrate in the present invention.
The following examples further describe and demonstrate embodiments within the scope of the present invention. These examples are given solely for the purpose of illustration and are not to be construed as limitations of the present invention as many variations thereof are possible without departing from the spirit and scope. All percentages used herein are by weight of the composition unless otherwise indicated.
93.7 g (i-e 0.67 mol) of allyl succinic anhydride, 52 g of toluene and 1.01 g of a Kardtedt catalyst solution (0.1% of Pt in hexamethyldisiloxane) are added into a 500 ml reactor. The reaction mass is heated at 90° C.; 120 g (i.e., 0.45 mol of SiH) of a polydimethylhydrogenosiloxane having the formula
Me3SiO(SiMe2O)9(SiMeHO)4SiMe3
and containing 3.75 mol of SiH/kg, are added over 3 hours. The SiH amount (determined by gazometry) transformed at the end of the addition is of 96.1%; it is of 100% 2 hours after the end of the addition. The volatiles are eliminated by evaporation under vacuum (3 mbar) over 10 hours at 150° C. 15 g of demineralized water are then added in order to hydrolyze the succinic anhydride functions. The hydrolysis reaction is followed by infrared analysis (acid band at 1714 cm−1, anhydride band at 1863 and 1782 cm−1). When the hydrolysis reaction is complete (48 hours), 100 g of toluene are added in order to azeotropically eliminate water. 133.5 g (corresponding to a yield of 82%) of a viscous oil are recovered.
NMR analysis confirmed the following general structure of the product obtained:
Me3SiO(SiMe2O)9(SiMeAO)4SiMe3
in which A represents —(CH2)3—CH(COOH)—CH2COOH Said product can be heated up to 60° C. and then dispersed by homogenization in a surfactant, if it is applied in a home care composition having an acid pH. Said product is water dispersible if the pH is above 10.
49.8 g (i-e 0.36 mol) of allyl succinic anhydride, 44 g of toluene and 1.139 g of a Kardtedt catalyst solution (0.1% of Pt in hexamethyldisiloxane) are added into a 500 ml reactor. The reaction mass is heated at 90° C.; 150.3 g (i.e., 0.266 mol of SiH) of a polydimethylhydrogenosiloxane having the formula
Me3SiO(SiMe2O)100(SiMeHO)15SiMe3
and containing 1.77 mol of SiH/kg, are added over 1 hour. The SiH amount (determined by gazometry) transformed at the end of the addition is of 86%; it is of 100% 16 hours after the end of the addition. The volatiles are eliminated by evaporation under vacuum (6 mbar) over 10 hours at 150° C. 101 g of toluene are added; the reaction mass is filtered. 6.7 g of demineralized water are then added in order to hydrolyze the succinic anhydride functions. The hydrolysis reaction is followed by infrared analysis (acid band at 1714 cm−1, anhydride band at 1866 and 1788 cm−1). When the hydrolysis reaction is complete (6 days), water is azeotropically eliminated. 146.3 g (corresponding to a yield of 80%) of a viscous oil are recovered.
NMR analysis confirmed the following general structure of the product obtained:
Me3SiO(SiMe2O)100(SiMeAO)15SiMe3
in which A represents —(CH2)3—CH(COOH)—CH2COOH
Glass cleaning formulations are recorded in the table below:
Evaluation Method
Glass slides (GS) of Obertrager type are treated by spraying the F1-F4 above formulations thereon. Then, they are either rinsed (R) with pure water or not rinsed (NR). The following treated glass slides are thus prepared:
A measurement of contact angle between water and the surface of each slide is carried out on a Ramé-Hart assembly. Then, each treated glass slide is stained by coating with a model stain formulation made of:
After a drying period of 15 minutes, each slide is rinsed with pure water. The amount of residual stain at the surface is evaluated through image analysis. The results are given in terms of amount of residual stain after rinsing as compared to the whole treated surface. 100% means that none of the stain is removed; the higher the amount of residual stain, the lower the performance of the product.
These results show that the product of Example 1 provides soil-release properties and prevents soil adhesion onto glass surfaces, eventhough hydrophilisation is not achieved. An anti-fogging benefit is also noted.
The above formulations F3 and F4 (or the same formulations with product of Example 2) can be used as an all purpose cleaner, particularly for cleaning windows or rinsing shower walls. They are used as is by spraying at the surfaces of the windows or the shower walls (3 to 5 g of formulation per m2 of surface). The products of example 1 or 2 confer on the surface efficient anti-fogging and soil repellency benefits.
Formulations C1-C4 recorded in the table below are tested with the same methodology as in example 3 on ceramic tiles (CT) (instead of glass slides). The results of stain removability on ceramic tiles are given in the table below
The above compositions C2-C4 (or the same compositions with the product of Example 2) can be used as rinse aid in automatic dishwashing or as toilet bowls cleaner.
Detergent formulations D1 and D2 recorded in the table below are tested on ceramic tiles with the classical soap scum test.
The stain composition is as follows:
Testing Procedure
The formulation is prepared from the components given in the table below.
The formulations of Examples 6 and 7 are used as is or they can be diluted before use, to a rate of 10 g of formulation in 1 litre of water.
They confer on the surface efficient soil repellency, shine, surface repair and next step easy cleaning benefit.
A base detergent formulation is prepared from the compounds given in the table below:
These formulations confer on the surface soil repellency, shine, surface repair and next step easy cleaning benefit.
The formulation is prepared from the components given in the table below.
The formulation is prepared from the components given in the table below.
Product of Example 1 is also found efficient in substantiating a peroxide containing formulation next to the toilet bowl surface. A bleach effect is sustainable up to a few hours after application of the product.
The formulation is prepared from the components given in the table below.
The formulation is prepared from the components given in the table below.
Aqueous biocidal compositions for hand dishwashing are prepared by using:
All documents cited in the Detailed Description of the Invention are, in relevant part, incorporated herein by reference; the citation of any document is not to be construed as an admission that it is prior art with respect to the present invention.
While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.
This application claims the benefit of U.S. Provisional Application No. 60/378,998, filed May 9, 2002.
Number | Name | Date | Kind |
---|---|---|---|
4405469 | Hafner et al. | Sep 1983 | A |
4658049 | Nakano et al. | Apr 1987 | A |
4859359 | DeMatteo et al. | Aug 1989 | A |
4876152 | Kang | Oct 1989 | A |
5063052 | Grollier et al. | Nov 1991 | A |
5087443 | Chizat et al. | Feb 1992 | A |
5516869 | Lucarelli et al. | May 1996 | A |
5702490 | Kneip et al. | Dec 1997 | A |
6007801 | Hossel et al. | Dec 1999 | A |
20030212231 | Olier | Nov 2003 | A1 |
Number | Date | Country |
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196 169 | Apr 1986 | EP |
Number | Date | Country | |
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20030212232 A1 | Nov 2003 | US |
Number | Date | Country | |
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60378998 | May 2002 | US |