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
  • C11D3/39—Organic or inorganic per-compounds
  • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
  • C11D3/3905—Bleach activators or bleach catalysts
  • C11D3/3907—Organic compounds
  • C11D3/3915—Sulfur-containing 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
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
  • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
• • 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
  • C11D3/39—Organic or inorganic per-compounds
  • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
  • C11D3/3905—Bleach activators or bleach catalysts
  • C11D3/3907—Organic compounds
  • C11D3/391—Oxygen-containing 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
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/39—Organic or inorganic per-compounds
  • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
  • C11D3/3905—Bleach activators or bleach catalysts
  • C11D3/3907—Organic compounds
  • C11D3/3917—Nitrogen-containing compounds
  • C11D3/3927—Quarternary 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
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/39—Organic or inorganic per-compounds
  • C11D3/3947—Liquid compositions

Definitions

• the present invention relates to liquid aqueous stable monopersulfate-containing compositions packaged in a UV resistant container.
• Liquid aqueous bleaching compositions suitable for example laundry applications are well known in the art. It is also known that bleaching compositions relying on hypochlorite as the bleaching agent can be preferred over oxygen beaches like hydrogen peroxide, mainly for performance reasons, especially at lower temperatures.
• hypochlorite bleaches there are some limitations to the convenience of hypochlorite bleaches.
• hypochlorite bleaching may cause yellowing and/or damage of the fabrics which are being bleached. This holds particularly true for synthetic fabrics and indeed there is a standing prejudice against using hypochlorite beaches on synthetic fibers, as evidenced by warnings on labels of commercially available hypochlorite bleaches.
• a variety of fabrics made of or containing synthetic fibers are labelled by their manufacturers as non-bleachable.
• Another drawback associated to hypochlorite based bleaching compositions is that undesirable typical chlorine odor may be perceived by the consumer during and after use, e.g., on the hands of the user or fabrics that have been bleached with such compositions.
• compositions according to the present invention being packaged in a UV light resistant container upon ageing of the composition, when used in various applications, e.g. in a laundry operation at a conventional dilution level of for example 100 ml/L to 1 ml/L (composition:water), as compared to the bleaching performance delivered by the same composition not packaged in a UV light resistant container.
• the present invention delivers a liquid aqueous bleaching composition which exhibits a great flexibility in the surfaces and soils it may bleach.
• the compositions according to the present invention are particularly suitable in any laundry application, e.g., as a laundry detergent or a laundry additive, and when used as a laundry pretreater or in other household applications like in hard surface cleaning applications.
• compositions of the present invention are suitable for the bleaching of different types of fabrics including natural fabrics, (e.g., fabrics made of cotton, and linen), synthetic fabrics such as those made of polymeric fibres of synthetic origin (e.g., polyamide-elasthane) as well as those made of both natural and synthetic fibres.
• synthetic fabrics such as those made of polymeric fibres of synthetic origin (e.g., polyamide-elasthane) as well as those made of both natural and synthetic fibres.
• the bleaching compositions of the present invention based on monopersulfate salt and optionally the activator compound described herein may be used on synthetic fabrics despite a standing prejudice against using bleaches on synthetic fabrics, as evidenced by warnings on labels of clothes and commercially available bleaching compositions like hypochlorite-containing compositions.
• compositions according to the present invention are able to perform in a variety of conditions, i.e., in hard and soft water as well as when used neat or diluted. More particularly, it has been found that the preferred liquid aqueous compositions of the present invention comprising a monopersulfate salt and a bleach activator as described herein, find a preferred application when used in their diluted form in any application and especially in any conventional laundry application. Indeed, upon dilution (typically at a dilution level of 20ml/L or more (composition:water)) the compositions of the present invention become less acidic, e.g., from a pH of about 1.5 to about 6.5 or more.
• compositions according to the present invention although delivering effective bleaching performance in their neat form surprisingly exhibit further enhanced bleaching performance in their diluted form.
• this pH jump effect allows to formulate acidic liquid aqueous compositions (i.e. pH below 7, preferably below 3 and more preferably below 2) which are physically and chemically stable upon prolonged periods of storage and which deliver outstanding bleaching performance under diluted usage conditions.
• compositions of the present invention exhibit also effective stain removal performance on various stains including enzymatic stains and/or greasy stains. Furthermore, when used in any hard-surface application these compositions have been found to deliver excellent limescale removal performance and to leave less streaking/filming on the surface treated as compared for example to hypochlorite based compositions. Thus, an advantage of the compositions herein is that it may not be necessary to rinse the surface with water after having treated it with a composition of the present invention, this especially when used in its diluted form.
• the present invention encompasses a liquid aqueous composition having a pH from 0.6 to 7 and comprising a monopersulfate salt and optionally a bleach activator selected from the group consisting of an aldehyde activator compound, a ketone activator compound, a halide activator compound and a mixture thereof, said composition being packaged in a UV light resistant container.
• the present invention further encompasses processes of treating a surface, e.g. a fabric or a hard-surface, starting from a liquid composition as defined herein packaged in a UV light resistant container.
• the processes of treating, especially bleaching fabrics include the steps of contacting said fabrics with the liquid composition according to the present invention packaged in a UV light resistant container, in its neat or diluted form, allowing said fabrics to remain in contact with said bleaching composition for a period of time sufficient to bleach said fabrics, and subsequently rinsing said fabrics with water.
• the processes of treating hard-surfaces herein include the steps of applying the compositions herein, packaged in a UV light resistant container to said hard-surfaces in their neat or diluted form, and optionally rinsing said hard-surfaces.
• the liquid bleaching composition is a liquid bleaching composition
• compositions according to the present invention are liquid compositions as opposed to a solid or a gas.
• liquid includes “pasty” compositions.
• the liquid compositions herein are aqueous compositions.
• the liquid compositions according to the present invention have a pH from 0.6 to 7.
• the pH of the compositions herein is from 0.6 to 6, more preferably from 0.8 to 4, even more preferably from 1 to 3 and most preferably from 1 to 2.
• Formulating the compositions according to the present invention in the acidic pH range is critical to the chemical stability of the compositions according to the present invention.
• the acidic pH controls/limits the formation of highly reactive species which are unstable in acidic medium like dioxirane upon storage, and thus contributes to the stability of the compositions for prolonged periods of storage.
• dioxirane may result from the reaction between the monopersulphate salt and the activator (aldehyde and/or ketone activator compound as described herein after).
• the pH of the compositions may be adjusted by any acidifying or alkalinizing agents known to those skilled in the art.
• acidifying agents are organic acids such as citric acid and inorganic acids such as sulphuric acid, sulphonic acid and/or metanesulphonic acid.
• alkalinizing agents are sodium hydroxide, potassium hydroxide and/or sodium carbonate.
• compositions according to the present invention comprise a monopersulfate salt or a mixture thereof.
• Suitable monopersulfate salts include any alkali metal monopersulfate salt including sodium monopersulfate salts and/or potassium monopersulfate salts.
• Examples of monomonopersulfate salts commercially available are those commercialised by Interox under the trade name Curox®, by Degussa under the trade name Caroat® or by DuPont under the trade name Oxone®. It is to understand herein that when the commercially available Curox®, Caroat® and/or Oxone® are used, the % weights of monopersulfate salts mentioned herein, refer to the total weight of said Curox®, Caroat® and/or Oxone®. The active concentration is approximately 1/2 of the total weight.
• compositions herein comprise from 0.01% to 50% by weight of the total composition of said monopersulfate salt or mixtures thereof, preferably from 0.5% to 20%, more preferably from 1% to 15% and most preferably from 2% to 10%.
• compositions of the present invention are physically and chemically stable upon prolonged periods of storage.
• compositions herein may be evaluated by measuring the concentration of available oxygen at given storage time after having manufactured the compositions.
• chemically stable it is meant herein that the compositions of the present invention comprising a monopersulfate salt or mixtures thereof and optionally the activator compound do not undergo more than 15% AvO loss, in one month at 25°C and preferably not more than 10%.
• AvO loss of a monopersulfate containing composition can be measured by titration with potassium permanganate after reduction with a solution containing ammonium ferrous sulphate. Said stability test method is well known in the art and is reported, for example, on the technical information sheet of Curox R commercially available from Interox. Alternatively monopersulfate concentration can also be measured using a chromatography method described in the literature for peracids (F. Di Furia et al., Gas-liquid Chromatography Method for Determination of Peracids, Analyst, Vol 113, May 1988, p 793-795).
• compositions of the present invention are packaged in a UV light resistant container.
• UV light resistant container it is meant any container that has a transmittance of UV-light (i.e., for the wavelengths from 400 nm to 200 nm) of less than 50%, preferably less than 30%, more preferably less than 10%, even more preferably less than 5% and most preferably of 0%.
• this container also has a transmittance of less than 70%, preferably less than 50%, more preferably less than 20% in the visible light (i.e., with wavelength from 700 nm to 401 nm). Transmittance can be measured by any spectrophotometric common test method.
• the UV light resistant containers for use herein can be made of any material known to those in the art provided it comprises a UV stabilizer (also called UV absorber ).
• the containers can be made of thermoplastic resins.
• the container may be made from a single material but also from a blend, a co-extruded or from a laminated material. It may be more or less rigid or may have parts which are more rigid than others, by modifying the thickness of the material used for example.
• Such resins may be made using various methods, including Ziegler Natta or Metallocene catalysis.
• Suitable thermoplastic resins for use herein include polyolefin resins preferably polyethylene and/or polypropylene.
• polyolefin resins preferably polyethylene and/or polypropylene.
• low density polyethylene high pressure branched homopolyethylene, LDPE
• linear low density polyethylene low pressure or modified high pressure ethylene- a- olefin copolymer, L-LDPE
• high density polyethylene high density polyethylene
• HDPE high density polyethylene
• EVA ethylene-vinyl acetate copolymer
• EVA ethylene-vinyl acetate copolymer
• PVC polypropylene
• PVDC vinylidene chloride-vinyl chloride copolymer
• EVOH ethylene-vinyl alcohol copolymer
• PVA polystyrene
• PS polystyrene
• the UV light resistant container herein contains more than 50% by weight of a thermoplastic resin or a mixture thereof, preferably more than 85% and more preferably more than 90%.
• the UV light resistant container herein comprises as an essential material a UV stabilizer or a mixture thereof. All the UV stabilizers currently used in the packaging field are suitable herein. Suitable UV stabilizers include oxides like silica, diatomaceous earth, aluminia, titanium dioxide, iron oxide, zinc oxide, magnesium oxide, antimony oxide, barium ferrite, strontium ferrite, beryllium oxide, pumice, pumice balloon, alumina fiber and the like, hydroxides like aluminium hydroxides, magnesium hydroxides, basic magnesium carbonate and the like, carbonates like calcium carbonate, magnesium carbonate, dolomite, sulphate, sulphites like calcium sulphate, barium sulphate, ammonium sulphate, calcium sulphite, silicates like talc, clay mica, asbestos, glass fiber, glass balloon, glass bead, calcium silicare, montmorillonite, bentonite, carbons like carbon black, graphite, carbon fiber, carbon hollow bead, as
• the UV light resistant container herein comprises from 0.01% to 30% by weight of the total container of a UV stabilizer or mixture thereof, preferably from 0.1% to 15% more preferably from 0.5% to 10%.
• the containers herein essential those made of thermoplastic resins may also include additional materials that do not affect its essential character, for instance stabilizers, pigments, processing aids such as waxes, deodorizing agents, anti-static agents, anti-blocking agents, plasticizers and the like.
• glass material modified with UV stabilizers may also be used.
• these containers include conventional bottles, bottles equipped with roll-on, sponge, brusher or sprayer, pouches, bags, gusset bags or plastified carboards (e.g. tetrapack®).
• Preferred containers for use herein are bottles made of thermoplastic resins comprising a UV stabiliser. Such bottles may be made by conventional manufacturing methods include blow moulding, extrusion and injection.
• compositions of the present invention being packaged in a UV light resistant container deliver effective stain removal performance and bleaching performance when used to bleach a surface, preferably in any laundry application, even upon ageing of the compositions, i.e. after prolonged periods of storage (typically up to 12 months at room temperature (about 20°C)).
• packing the compositions herein in such UV light resistant containers maintains the properties associated to these compositions upon prolonged periods of time after their manufacturing.
• liquid aqueous compositions of the present invention are particularly safe to both the fabrics bleached therewith and colours in a typical laundry soaking operation, as compared to a soaking operation with solid (granular) monopersulfate salt-containing compositions.
• compositions according to the present invention may comprise an aldehyde activator compound, a ketone activator compound, a halide activator compound or a mixture thereof.
• aldehyde it is meant herein any compound which contains at least one carbonyl group and has two hydrogen atoms or carbon atom and a hydrogen atom attached directly to at least one of the carbonyl carbon atoms.
• ketone it is meant herein any compound which contains at least one carbonyl group and has two carbon atoms attached directly to at least one of the carbonyl carbon atoms.
• These compounds can be aliphatic or aromatic substituted or unsubstituted, saturated or unsaturated, or acyclic, carbocyclic or heterocyclic.
• halide it is meant chloride, bromide and/or iodide.
• activator it is meant herein ketone, aldehyde and halide compounds and mixtures thereof that react with monopersulfate salt to form an activated bleaching specie, i.e. a dioxirane (when the activator compound is ketone or aldehyde) or a hypohalogenite (when the activator compound is a halide).
• activated bleaching specie i.e. a dioxirane (when the activator compound is ketone or aldehyde) or a hypohalogenite (when the activator compound is a halide).
• activated species i.e. dioxirane and hypohalogenite
• dioxirane and hypohalogenite which are thought to greatly enhance the bleaching in the present invention over monopersulfate alone or over other activated bleaching system, e.g. hydrogen peroxide and acetyl triethyl citrate.
• activated bleaching system e.g. hydrogen peroxide and acetyl triethyl citrate.
• These activation mechanisms mainly occur upon dilution of the compositions herein with water and are emphased with the pH jump in the neutral to alkaline pH range (i.e. around 6 and higher) associated to this dilution. It is at those pHs that more dioxiranes and/or hypohalogenites are generated thereby outstandingly improving the bleaching performance of the compositions of the present invention.
• Suitable aldehyde activator compounds for use herein include chloral-hydrate, acetaldehyde, butyraldehyde, benzaldehyde, and/or 4-trimethylammonio benzaldehyde methyl sulfate.
• Particularly preferred aldehyde activator compounds for use herein are acetaldehyde, butyraldehyde and/or, benzaldehyde and most preferred is acetaldehyde.
• Aldehyde activator compounds are in general less preferred than the ketone activators compounds as they may be oxidised during prolonged storage periods.
• acetaldehyde may be commercially available from Aldrich.
• Suitable aliphatic ketone activator compounds for use herein include acetacetone, 2,3-hexanedione, trimethylammonio acetone nitrate, 5-diethylbenzylammonio 2-pentanone nitrate, 5-diethylmethylammonio 2-pentanone nitrate, methyl pyruvate, diethyl keto malonate, 3-hydroxy-2-butanone, acetol, hexachloracetone, 2,5-hexanedione, phenylacetone, ethyl levulinate, 3-hydroxy-2-pentanone, acetone, 3-penten-2-one, methyl ethyl ketone, 4-hydroxy-3-methyl-2-butanone, 3-pentanone, and/or 2-heptanone.
• acetacetone may be commercially available from Aldrich under its chemical name.
• Suitable aromatic ketone activator compounds for use herein include hydroxyquinoline, 4-acetyl-1-methylpyridinium nitrate, di-2-pyridyl ketone N-oxide, 2-acetylquinoxaline, 2-acetyl-3-methylquinoxaline oxaline, di-2- pyridyl ketone, 6-acetyl-1,2,4-trimethyl quinolinium nitrate, 8-hydroxyquinoline N-oxide, methyl phenyl glyoxalate, N-methyl-p-morpholinio acetophenone methyl sulfate, 3-acetyl pyridine N-oxide, p-nitroacetophenone, m-nitroacetophenone, sodium p-acetyl benzene sulfonate, p-acetylbenzonitrile, 3,5-dinitroacetophenone, 4-trimethylammonioacetophenone nitrate, 4-methoxy-3-
• Suitable cyclic ketone activator compounds for use herein include cyclohexanone, 2-methylcyclohexanone, 2,6-dimethyl cyclohexanone, 3-methyl cyclohexanone, 4-ethyl cyclohexanone, 4-t-butyl cyclohexanone, 4,4-dimethyl cyclohexanone, methyl 4-oxo-cyclohexanone carboxylate, sodium 4-oxo-cyclohexanone carboxylate, 2-trimethylammoniocyclohexanone nitrate, 4-trimethylammonio cyclohexanone nitrate, 3 oxo-cyclohexyl acetic acid, cycloheptanone, 1,4-cyclohexadione, dehydrochloric acid, tropinone methonitrate, N-methyl-3-oxoquinuclidinium nitrate, cyclooctanone and/or cyclopentan
• cyclohexanone may be commercially available from Aldrich under its chemical name.
• Suitable heterocyclic ketone activator compounds for use herein include, 2,2,6,6-tetramethyl-4-piperidone hydrate, 1-methyl-4-piperidone N-oxide, N-carbethoxy 4-piperidone, tetrahydrothiopyran-4-one methonitrate, tetrahydrothiopyran-4-one S,S- dioxide, tetrahydrothiopyran-3-one,S,S,-dioxide, and/or 4-oxacyclohexanone.
• Particularly preferred bleach activators for use herein are the ketone activator compounds and highly preferred are the ketones activator compounds bearing a positive charge.
• oxopiperidinium salts particularly suitable for use herein include 1,1-dimethyl-3-oxopiperidinium nitrate, 1,1-dimethyl-4-oxopiperidinium triflate, 1,1-dimethyl-3-oxopiperidinium triflate, 1,1-dimethyl-4-oxopiperidinium nitrate, 1-benzyl-4-piperidone methonitrate, 1-t-butyl-1-methyl-4-oxopiperidinium nitrate, 1-(4-dodecylbenzyl) 1-methyl-4 oxopiperidinium chloride, 3-(N-methyl-4 oxopiperidinium)-propane sulfonate, 1-allyl-1-methyl-4- oxopiperidinium chloride, 1-methyl-1-(1-naphthyl-methyl)-4- oxopiperidinium chloride, 1-methyl-1-pentamethylbenzyl- 4-oxopiperidinium chloride, N,N'-
• ketone activator compounds bearing a positive charge suitable for use herein are for example the ammonium acetophenone salts according to the following formula: wherein the ammonium group can be either at the 2 , at the 3 position or at the 4 position ;
• R1, R2 and R3 are each independently a substituted or unsubstituted hydrocarbon group having from 1 to 20 carbon atoms, preferably a substituted or unsubstituted alkyl, or alkenyl or alkinyl group containing from 1 to 20 carbon atoms, preferably from 1 to 12 carbon atoms, or a substituted or unsubstituted aryl group containing from 6 to 10 atoms or a C1-C20 alkyl aryl group wherein the aryl group contains from 6 to 10 carbon atoms;
• R4 is a substituted or nonsubstituted halogenate alkyl group having from 1 to 20 carbon atoms, preferably from 1 to 12 carbon atoms and more preferably is
• ammonium acetophenone salts for use herein include 4-trimethylammonium acetophenone nitrate, 2-trimethylammoniumacetophenone nitrate, 4-triethylammoniumacetophenone mesilate, 3-trimethylammoniumacetophenone mesilate, trihalogenatedmethylphenyl ketone like trifluoromethylphenylketone, trichloromethylphenylketone, tribromomethylphenylketone or a mixture thereof.
• Suitable halide activator compounds for use herein include chloride, bromide, iodide and mixtures thereof. Particularly preferred halide activator compounds for use herein is an alkali metal of chloride. For example sodium chloride may be commercially available from Aldrich under its chemical name.
• compositions herein may comprise from 0.01% to 10% by weight of the total composition of said ketone, aldehyde and/or halide activator compound, preferably from 0.05% to 5%, more preferably from 0.1% to 2% and most preferably from 0.2% to 1.5%.
• this activated bleaching system provides effective bleaching performance on a variety of soils, from hydrophobic to hydrophilic soils under any household application and especially laundry application on both hydrophilic and hydrophobic fabrics.
• the present invention provides not only effective bleaching performance but also good stain removal performance of various types of stains including greasy stains (e.g., lipstick, tomato, make-up) and/or enzymatic stains (e.g. blood, choco pudding), as compared to the same formulation without said activator compounds as described herein.
• greasy stains e.g., lipstick, tomato, make-up
• enzymatic stains e.g. blood, choco pudding
• the bleaching performance may be evaluated by the following test methods on various type of bleachable stains.
• a suitable test method for evaluating the bleaching performance on a soiled fabric under diluted conditions is the following: A composition according to the present invention packaged in a UV light resistant container, is diluted after for example 6 months storage time at 20°C, with water typically at a dilution level of 1 to 100 ml/L, preferably 20 ml/L (composition :water), then the soiled fabrics are soaked in it for 20 minutes to 6 hours and then rinsed.
• the bleaching composition can be used in a washing machine at a dilution level of typically at a dilution level of 1 to 100 ml/L (composition :water).
• the soiled fabrics are washed at a temperature of from 30° to 70°C for 10 to 100 minutes and then rinsed.
• the reference composition i.e., same composition at same storage time but not packaged in an UV light resistant container
• Soiled fabrics/swatches with for example tea, coffee and the like may be commercially available from E.M.C. Co. Inc..
• the bleaching performance is then evaluated by comparing side by side the soiled fabrics treated with the composition of the present invention with those treated with the reference.
• a visual grading may be used to assign difference in panel units (psu) in a range from 0 to 4.
• compositions herein may further comprise a variety of other optional ingredients such as surfactants, chelating agents, radical scavengers, antioxidants, other stabilisers, builders, soil suspenders, polymeric soil release agents, catalysts, dye transfer agents, solvents, suds controlling agents, brighteners, perfumes, pigments, dyes and the like.
• surfactants such as surfactants, chelating agents, radical scavengers, antioxidants, other stabilisers, builders, soil suspenders, polymeric soil release agents, catalysts, dye transfer agents, solvents, suds controlling agents, brighteners, perfumes, pigments, dyes and the like.
• compositions of the present invention may comprise a surfactant or a mixture thereof including nonionic surfactants, anionic surfactants, cationic surfactants, zwitterionic surfactants and/or amphoteric surfactants.
• these surfactants do not contain functional groups that can be oxidised by the monopersulphate salt, or that can substantially hydrolize at a low pH.
• compositions according to the present invention may comprise from 0.01% to 50% by weight of the total composition of a surfactant or a mixture thereof, preferably from 0.1% to 30 % and more preferably from 0.2% to 10%.
• Suitable anionic surfactants for use in the compositions herein include water-soluble salts or acids of the formula ROSO 3 M wherein R preferably is a C 10 -C 24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C 10 -C 20 alkyl component, more preferably a C 12 -C 18 alkyl or hydroxyalkyl, and M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium), or ammonium or substituted ammonium (e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethylammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
• alkyl chains
• Suitable anionic surfactants for use herein are water-soluble salts or acids of the formula RO(A) m SO 3 M wherein R is an unsubstituted C 10 -C 24 alkyl or hydroxyalkyl group having a C 10 -C 24 alkyl component, preferably a C 12 -C 20 alkyl or hydroxyalkyl, more preferably C 12 -C 18 alkyl or hydroxyalkyl, A is an ethoxy or propoxy unit, m is greater than zero, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3, and M is H or a cation which can be, for example, a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium, etc.), ammonium or substituted-ammonium cation.
• R is an unsubstituted C 10 -C 24 alkyl or hydroxyalkyl group having a C 10 -C 24 alkyl component, preferably a C 12 -C
• Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
• Specific examples of substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium and quaternary ammonium cations, such as tetramethyl-ammonium, dimethyl piperdinium and cations derived from alkanolamines such as ethylamine, diethylamine, triethylamine, mixtures thereof, and the like.
• Exemplary surfactants are C 12 -C 18 alkyl polyethoxylate (1.0) sulfate, C 12 -C 18 E(1.0)M), C 12 -C 18 alkyl polyethoxylate (2.25) sulfate, C 12 -C 18 E(2.25)M), C 12 -C 18 alkyl polyethoxylate (3.0) sulfate C 12 -C 18 E(3.0), and C 12 -C 18 alkyl polyethoxylate (4.0) sulfate C 12 -C 18 E(4.0)M), wherein M is conveniently selected from sodium and potassium.
• alkyl sulphonates including water-soluble salts or acids of the formula RSO 3 M wherein R is a C 6 -C 22 linear or branched, saturated or unsaturated alkyl group, preferably a C 12 -C 18 alkyl group and more preferably a C 14 -C 16 alkyl group, and M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium), or ammonium or substituted ammonium (e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethyl-ammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
• R is a C 6 -C 22 linear or branched, saturated
• Suitable alkyl aryl sulphonates for use herein include water- soluble salts or acids of the formula RSO 3 M wherein R is an aryl, preferably a benzyl, substituted by a C 6 -C 22 linear or branched saturated or unsaturated alkyl group, preferably a C 12 -C 18 alkyl group and more preferably a C 14 -C 16 alkyl group, and M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium, calcium, magnesium etc) or ammonium or substituted ammonium (e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethyl-ammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethy
• alkylsulfonates and alkyl aryl sulphonates for use herein include primary and secondary alkylsulfonates and primary and secondary alkyl aryl sulphonates.
• secondary C6-C22 alkyl or C6-C22 alkyl aryl sulphonates it is meant herein that in the formula as defined above, the SO3M or aryl-SO3M group is linked to a carbon atom of the alkyl chain being placed between two other carbons of the said alkyl chain (secondary carbon atom).
• C14-C16 alkyl sulphonate salt is commercially available under the name Hostapur ® SAS from Hoechst and C8-alkylsulphonate sodium salt is commercially available under the name Witconate NAS 8® from Witco SA.
• An example of commercially available alkyl aryl sulphonate is Lauryl aryl sulphonate from Su.Ma.
• Particularly preferred alkyl aryl sulphonates are alkyl benzene sulphonates commercially available under trade name Nansa® available from Albright&Wilson.
• anionic surfactants useful for detersive purposes can also be used herein. These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, C 8 -C 24 olefinsulfonates, sulfonated polycarboxylic acids prepared by sulfonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British patent specification No.
• alkylpolyglycolethersulfates (containing up to 10 moles of ethylene oxide); alkyl ester sulfonates such as C 14 - 16 methyl ester sulfonates; acyl glycerol sulfonates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates, isethionates such as the acyl isethionates, N-acyl taurates, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C 12 -C 18 monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C 6 -C 14 diesters), sulfates of alkylpolysaccharides such as the sulfates
• Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil. Further examples are given in "Surface Active Agents and Detergents" (Vol. I and II by Schwartz, Perry and Berch). A variety of such surfactants are also generally disclosed in U.S. Patent 3,929,678, issued December 30, 1975, to Laughlin, et al. at Column 23, line 58 through Column 29, line 23 (herein incorporated by reference).
• alkyl carboxylates and alkyl alkoxycarboxylates having from 4 to 24 carbon atoms in the alkyl chain, preferably from 8 to 18 and more preferably from 8 to 16, wherein the alkoxy is propoxy and/or ethoxy and preferably is ethoxy at an alkoxylation degree of from 0.5 to 20, preferably from 5 to 15.
• Suitable amphoteric surfactants for use herein include amine oxides having the following formula R 1 R 2 R 3 NO wherein each of R1, R2 and R3 is independently a saturated substituted or unsubstituted, linear or branched hydrocarbon chains of from 1 to 30 carbon atoms.
• Preferred amine oxide surfactants to be used according to the present invention are amine oxides having the following formula R 1 R 2 R 3 NO wherein R1 is an hydrocarbon chain comprising from 1 to 30 carbon atoms, preferably from 6 to 20, more preferably from 8 to 16, most preferably from 8 to 12, and wherein R2 and R3 are independently substituted or unsubstituted, linear or branched hydrocarbon chains comprising from 1 to 4 carbon atoms, preferably from 1 to 3 carbon atoms, and more preferably are methyl groups.
• R1 may be a saturated substituted or unsubstituted linear or branched hydrocarbon chain.
• Suitable amine oxides for use herein are for instance natural blend C8-C10 amine oxides as well as C12-C16 amine oxides commercially available from Hoechst.
• Suitable zwitterionic surfactants for use herein contain both a cationic hydrophilic group, i.e., a quaternary ammonium group, and anionic hydrophilic group on the same molecule at a relatively wide range of pH's.
• the typical anionic hydrophilic groups are carboxylates and sulfonates, although other groups like sulfates, phosphonates, and the like can be used.
• R 1 -N + (R 2 )(R 3 )R 4 X - wherein R 1 is a hydrophobic group; R 2 is hydrogen, C 1 -C 6 alkyl, hydroxy alkyl or other substituted C 1 -C 6 alkyl group; R 3 is C 1 -C 6 alkyl, hydroxy alkyl or other substituted C 1 -C 6 alkyl group which can also be joined to R 2 to form ring structures with the N, or a C 1 -C 6 carboxylic acid group or a C 1 -C 6 sulfonate group; R 4 is a moiety joining the cationic nitrogen atom to the hydrophilic group and is typically an alkylene, hydroxy alkylene, or polyalkoxy group containing from 1 to 10 carbon atoms; and X is the hydrophilic group which is a carboxylate or sulfonate group.
• R 1 are aliphatic or aromatic, saturated or unsaturated, substituted or unsubstituted hydrocarbon chains that can contain linking groups such as amido groups, ester groups. More preferred R 1 is an alkyl group containing from 1 to 24 carbon atoms, preferably from 8 to 18, and more preferably from 10 to 16. These simple alkyl groups are preferred for cost and stability reasons.
• the hydrophobic group R 1 can also be an amido radical of the formula R a -C(O)-NH-(C(R b ) 2 ) m , wherein R a is an aliphatic or aromatic, saturated or unsaturated, substituted or unsubstituted hydrocarbon chain, preferably an alkyl group containing from 8 up to 20 carbon atoms, preferably up to 18, more preferably up to 16, R b is selected from the group consisting of hydrogen and hydroxy groups, and m is from 1 to 4, preferably from 2 to 3, more preferably 3, with no more than one hydroxy group in any (C(R b ) 2 ) moiety.
• Preferred R 2 is hydrogen, or a C 1 -C 3 alkyl and more preferably methyl.
• Preferred R 3 is a C 1 -C 4 carboxylic acid group or C1-C4 sulfonate group, or a C 1 -C 3 alkyl and more preferably methyl.
• Preferred R 4 is (CH2) n wherein n is an integer from 1 to 10, preferably from 1 to 6, more preferably is from 1 to 3.
• betaine/sulphobetaine Some common examples of betaine/sulphobetaine are described in U.S. Pat. Nos. 2,082,275, 2,702,279 and 2,255,082, incorporated herein by reference.
• alkyldimethyl betaines examples include coconut-dimethyl betaine, lauryl dimethyl betaine, decyl dimethyl betaine, 2-(N-decyl-N, N-dimethyl-ammonia)acetate, 2-(N-coco N, N-dimethylammonio) acetate, myristyl dimethyl betaine, palmityl dimethyl betaine, cetyl dimethyl betaine, stearyl dimethyl betaine.
• coconut dimethyl betaine is commercially available from Seppic under the trade name of Amonyl 265®.
• Lauryl betaine is commercially available from Albright & Wilson under the trade name Empigen BB/L®.
• amidobetaines include cocoamidoethylbetaine, cocoamidopropyl betaine or C10-C14 fatty acylamidopropylene(hydropropylene)sulfobetaine.
• C10-C14 fatty acylamidopropylene(hydropropylene)sulfobetaine is commercially available from Sherex Company under the trade name "Varion CAS® sulfobetaine".
• betaine is Lauryl-immino-dipropionate commercially available from Rhone-Poulenc under the trade name Mirataine H2C-HA ®.
• Suitable cationic surfactants for use herein include derivatives of quaternary ammonium, phosphonium, imidazolium and sulfonium compounds.
• Preferred cationic surfactants for use herein are quaternary ammonium compounds wherein one or two of the hydrocarbon groups linked to nitrogen are a saturated, linear or branched alkyl group of 6 to 30 carbon atoms, preferably of 10 to 25 carbon atoms, and more preferably of 12 to 20 carbon atoms, and wherein the other hydrocarbon groups (i.e.
• quaternary ammonium compounds suitable for use herein are non-chloride/non halogen quaternary ammonium compounds.
• the counterion used in said quaternary ammonium compounds are compatible with any monopersulfate salt and are selected from the group of methyl sulfate, or methylsulfonate, and the like.
• compositions of the present invention are trimethyl quaternary ammonium compounds like myristyl trimethylsulfate, cetyl trimethylsulfate and/or tailow trimethylsulfate.
• trimethyl quaternary ammonium compounds are commercially available from Hoechst, or from Albright & Wilson under the trade name EMPIGEN CM®.
• alkoxylated nonionic surfactants and especially ethoxylated nonionic surfactants are suitable for use herein.
• Capped alkoxylated nonionic surfactants are particularly suitable for use herein as they have improved stability to the monopersulfate salts.
• Suitable capped alkoxylated nonionic surfactants for use herein are according to the formula: R 1 (O-CH 2 -CH 2 ) n -(OR 2 ) m -O-R 3 wherein R 1 is a C 8 -C 24 linear or branched alkyl or alkenyl group, aryl group, alkaryl group, preferably R 1 is a C 8 -C 18 alkyl or alkenyl group, more preferably a C 10 -C 15 alkyl or alkenyl group, even more preferably a C 10 -C 15 alkyl group; wherein R 2 is a C 1 -C 10 linear or branched alkyl group, preferably a C 2 -C 10 linear or branched alkyl group; wherein R 3 is a C 1 -C 10 alkyl or alkenyl group, preferably a C 1 -C 5 alkyl group, more preferably methyl; and wherein n and m are integers independently
• surfactants are commercially available from BASF under the trade name Plurafac®, from HOECHST under the trade name Genapol® or from ICI under the trade name Symperonic®.
• Preferred capped nonionic alkoxylated surfactants of the above formula are those commercially available under the tradename Genapol® L 2.5 NR from Hoechst, and Plurafac® from BASF.
• compositions of the present invention may comprise a cheating agent as a preferred optional ingredient.
• Suitable chelating agents may be any of those known to those skilled in the art such as the ones selected from the group comprising phosphonate chelating agents, amino carboxylate chelating agents, other carboxylate chelating agents, polyfunctionally-substituted aromatic chelating agents, ethylenediamine N,N'- disuccinic acids, or mixtures thereof.
• chelating agents contribute to further enhance the chemical stability of the compositions.
• a chelating agent may be also desired in the compositions of the present invention as it allows to increase the ionic strength of the compositions herein and thus their stain removal and bleaching performance on various surfaces.
• Suitable phosphonate chelating agents for use herein may include alkali metal ethane 1-hydroxy diphosphonates (HEDP), alkylene poly (alkylene phosphonate), as well as amino phosphonate compounds, including amino aminotri(methylene phosphonic acid) (ATMP), nitrilo trimethylene phosphonates (NTP), ethylene diamine tetra methylene phosphonates, and diethylene triamine penta methylene phosphonates (DTPMP).
• the phosphonate compounds may be present either in their acid form or as salts of different cations on some or all of their acid functionalities.
• Preferred phosphonate chelating agents to be used herein are diethylene triamine penta methylene phosphonate (DTPMP) and ethane 1-hydroxy diphosphonate (HEDP). Such phosphonate chelating agents are commercially available from Monsanto under the trade name DEQUEST®.
• Polyfunctionally-substituted aromatic chelating agents may also be useful in the compositions herein. See U.S. patent 3,812,044, issued May 21, 1974, to Connor et al.
• Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as 1,2-dihydroxy -3,5-disulfobenzene.
• a preferred biodegradable chelating agent for use herein is ethylene diamine N,N'- disuccinic acid, or alkali metal, or alkaline earth, ammonium or substitutes ammonium salts thereof or mixtures thereof.
• Ethylenediamine N,N'- disuccinic acids, especially the (S,S) isomer have been extensively described in US patent 4, 704, 233, November 3, 1987, to Hartman and Perkins.
• Ethylenediamine N,N'- disuccinic acids is, for instance, commercially available under the tradename ssEDDS® from Palmer Research Laboratories.
• Suitable amino carboxylates to be used herein include ethylene diamine tetra acetates, diethylene triamine pentaacetates, diethylene triamine pentaacetate (DTPA),N- hydroxyethylethylenediamine triacetates, nitrilotri-acetates, ethylenediamine tetrapropionates, triethylenetetraaminehexa-acetates, ethanoldiglycines, propylene diamine tetracetic acid (PDTA) and methyl glycine di-acetic acid (MGDA), both in their acid form, or in their alkali metal, ammonium, and substituted ammonium salt forms.
• PDTA propylene diamine tetracetic acid
• MGDA methyl glycine di-acetic acid
• Particularly suitable amino carboxylates to be used herein are diethylene triamine penta acetic acid, propylene diamine tetracetic acid (PDTA) which is, for instance, commercially available from BASF under the trade name Trilon FS® and methyl glycine di-acetic acid (MGDA).
• PDTA propylene diamine tetracetic acid
• MGDA methyl glycine di-acetic acid
• carboxylate chelating agents to be used herein include salicylic acid, aspartic acid, glutamic acid, glycine, malonic acid or mixtures thereof.
• R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of -H, alkyl, alkoxy, aryl, aryloxy, -Cl, -Br, -NO 2 , -C(O)R', and - SO 2 R''; wherein R' is selected from the group consisting of -H, -OH, alkyl, alkoxy, aryl, and aryloxy; R'' is selected from the group consisting of alkyl, alkoxy, aryl, and aryloxy; and R 5 , R 6 , R 7 , and R 8 are independently selected from the group consisting of -H and alkyl.
• Particularly preferred chelating agents to be used herein are amino aminotri(methylene phosphonic acid), di-ethylene-triamino-pentaacetic acid, diethylene triamine penta methylene phosphonate, 1-hydroxy ethane diphosphonate, ethylenediamine N, N'-disuccinic acid, and mixtures thereof.
• compositions according to the present invention comprise up to 5% by weight of the total composition of a chelating agent, or mixtures thereof, preferably from 0.01% to 1.5% by weight and more preferably from 0.01% to 0.5%.
• compositions of the present invention may comprise a radical scavenger or a mixture thereof.
• Suitable radical scavengers for use herein include the well-known substituted mono and dihydroxy benzenes and their analogs, alkyl and aryl carboxylates and mixtures thereof.
• Preferred such radical scavengers for use herein include di-tert-butyl hydroxy toluene (BHT), hydroquinone, di-tert-butyl hydroquinone, mono-tert-butyl hydroquinone, tert-butyl-hydroxy anysole, benzoic acid, toluic acid, catechol, t-butyl catechol, benzylamine, 1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenyl) butane, n-propyl-gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene.
• Such radical scavengers like N-propyl-gallate may be commercially available from Nipa Laboratories under the trade name Nip
• Radical scavengers when used are typically present herein in amounts up to 10% by weight of the total composition and preferably from 0.001% to 0.5% by weight.
• radical scavengers may contribute to the chemical stability of the bleaching compositions of the present invention as well as to the safety profile of the compositions of the present invention.
• compositions according to the present invention may further comprise a suds controlling agent such as 2-alkyl alkanol, or mixtures thereof, as a preferred optional ingredient.
• a suds controlling agent such as 2-alkyl alkanol, or mixtures thereof, as a preferred optional ingredient.
• Particularly suitable to be used in the present invention are the 2-alkyl alkanols having an alkyl chain comprising from 6 to 16 carbon atoms, preferably from 8 to 12 and a terminal hydroxy group, said alkyl chain being substituted in the ⁇ position by an alkyl chain comprising from 1 to 10 carbon atoms, preferably from 2 to 8 and more preferably 3 to 6.
• Such suitable compounds are commercially available, for instance, in the Isofol® series such as Isofol® 12 (2-butyl octanol) or Isofol® 16 (2-hexyl decanol).
• suds controlling agents may include alkali metal (e.g., sodium or potassium) fatty acids, or soaps thereof, containing from about 8 to about 24, preferably from about 10 to about 20 carbon atoms.
• alkali metal e.g., sodium or potassium
• soaps thereof containing from about 8 to about 24, preferably from about 10 to about 20 carbon atoms.
• the fatty acids including those used in making the soaps can be obtained from natural sources such as, for instance, plant or animal-derived glycerides (e.g., palm oil, coconut oil, babassu oil, soybean oil, castor oil, tallow, whale oil, fish oil, tallow, grease, lard and mixtures thereof).
• plant or animal-derived glycerides e.g., palm oil, coconut oil, babassu oil, soybean oil, castor oil, tallow, whale oil, fish oil, tallow, grease, lard and mixtures thereof.
• the fatty acids can also be synthetically prepared (e.g., by oxidation of petroleum stocks or by the Fischer-Tropsch process).
• Alkali metal soaps can be made by direct saponification of fats and oils or by the neutralization of the free fatty acids which are prepared in a separate manufacturing process. Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium and potassium tallow and coconut soaps.
• tallow is used herein in connection with fatty acid mixtures which typically have an approximate carbon chain length distribution of 2.5% C14, 29% C16, 23% C18, 2% palmitoleic, 41.5% oleic and 3% linoleic (the first three fatty acids listed are saturated). Other mixtures with similar distribution, such as the fatty acids derived from various animal tallows and lard, are also included within the term tallow.
• the tallow can also be hardened (i.e., hydrogenated) to convert part or all of the unsaturated fatty acid moieties to saturated fatty acid moieties.
• coconut refers to fatty acid mixtures which typically have an approximate carbon chain length distribution of about 8% C8, 7% C10, 48% C12, 17% C14, 9% C16, 2% C18, 7% oleic, and 2% linoleic (the first six fatty acids listed being saturated).
• Other sources having similar carbon chain length distribution such as palm kernel oil and babassu oil are included with the term coconut oil.
• Suitable suds controlling agents are exemplified by silicones, and silica-silicone mixtures.
• Silicones can be generally represented by alkylated polysiloxane materials while silica is normally used in finely divided forms exemplified by silica aerogels and xerogels and hydrophobic silicas of various types. These materials can be incorporated as particulates in which the suds controlling agent is advantageously releasably incorporated in a water-soluble or water-dispersible, substantially non-surface-active detergent impermeable carrier.
• the suds controlling agent can be dissolved or dispersed in a liquid carrier and applied by spraying on to one or more of the other components.
• a preferred silicone suds controlling agent is disclosed in Bartollota et al. U.S. Patent 3 933 672.
• Other particularly useful suds controlling agents are the self-emulsifying silicone suds controlling agents, described in German Patent Application DTOS 2 646 126 published April 28, 1977.
• An example of such a compound is DC-544, commercially available from Dow Corning, which is a siloxane-glycol copolymer.
• compositions can comprise a silicone/silica mixture in combination with fumed nonporous silica such as Aerosil R .
• Especially preferred suds controlling agent are the suds controlling agent system comprising a mixture of silicone oils and the 2-alkyl-alcanols.
• compositions herein may comprise up to 4% by weight of the total composition of a suds controlling agent, or mixtures thereof, preferably from 0.1% to 1.5% and most preferably from 0.1% to 0.8%.
• liquid aqueous composition of the present invention packaged in a UV light resistant container needs to be contacted with the surface to treat.
• surfaces any inanimate surface.
• inanimate surfaces include, but are not limited to, hard-surfaces typically found in houses like kitchens, bathrooms, or in car interiors, e.g., tiles, walls, floors, chrome, glass, smooth vinyl, any plastic, plastified wood, table top, sinks, cooker tops, dishes, sanitary fittings such as sinks, showers, shower curtains, wash basins, WCs and the like, as well as fabrics including clothes, curtains, drapes, bed linens, bath linens, table cloths, sleeping bags, tents, upholstered furniture and the like, and carpets.
• Inanimate surfaces also include household appliances including, but not limited to, refrigerators, freezers, washing machines, automatic dryers, ovens, microwave ovens, dishwashers and so on.
• bleaching and/or disinfecting said surfaces as the compositions of the present invention comprise a bleaching system based of monopersulfate salt and optionally a ketone, aldehyde or halide activator compound or a mixture thereof and optionally cleaning as said compositions may comprise a surfactant or any other conventional cleaning agents.
• the present invention also encompasses a process of treating, especially bleaching a fabric, as the inanimate surface.
• a composition according to the present invention packaged in a UV light resistant container, is contacted with the fabrics to be treated.
• pretreatment mode where a liquid bleaching composition, as defined herein, is applied neat onto said fabrics before the fabrics are rinsed, or washed then rinsed, or in a "soaking mode” where a liquid bleaching composition, as defined herein, is first diluted in an aqueous bath and the fabrics are immersed and soaked in the bath, before they are rinsed, or in a "through the wash mode", where a liquid bleaching composition, as defined herein, is added on top of a wash liquor formed by dissolution or dispersion of a typical laundry detergent. It is also essential in both cases, that the fabrics be rinsed after they have been contacted with said composition, before said composition has completely dried off.
• the processes of bleaching surfaces according to the present invention delivers effective whiteness performance as well as effective stain removal performance.
• compositions according to the present invention are preferably contacted to fabrics in a liquid form. Indeed, by "in a liquid form”, it is meant herein the liquid compositions according to the present invention per se in neat or in their diluted form.
• compositions according to the present invention are typically used in diluted form in a laundry operation.
• in diluted form it is meant herein that the compositions for the bleaching of fabrics according to the present invention may be diluted by the user, preferably with water. Such dilution may occur for instance in hand laundry applications as well as by other means such as in a washing machine.
• Said compositions can be diluted up to 500 times, preferably from 5 to 200 times and more preferably from 10 to 80 times.
• the process of bleaching fabrics according to the present invention comprises the steps of first contacting said fabrics with a bleaching composition according to the present invention, packaged in a UV light resistant container, in its diluted form, then allowing said fabrics to remain in contact with said composition, for a period of time sufficient to bleach said fabrics, typically 1 to 60 minutes, preferably 5 to 30 minutes, then rinsing said fabrics with water. If said fabrics are to be washed, i.e., with a conventional composition comprising at least one surface active agent, said washing may be conducted together with the bleaching of said fabrics by contacting said fabrics at the same time with a bleaching composition according to the present invention and said detergent composition, or said washing may be conducted before or after that said fabrics have been bleached.
• said process according to the present invention allows to bleach fabrics and optionally to wash fabrics with a detergent composition comprising at least one surface active agent before the step of contacting said fabrics with said bleaching composition and/or in the step where said fabrics are contacted with said bleaching composition and/or after the step where said fabrics are contacted with said bleaching composition and before the rinsing step and/or after the rinsing step.
• the process of bleaching fabrics comprises the step of contacting fabrics with a liquid bleaching composition according to the present invention, packaged in a UV light resistant container, in its neat form, of allowing said fabrics to remain in contact with said bleaching composition for a period of time sufficient to bleach said fabrics, typically 5 seconds to 30 minutes, preferably 1 minute to 10 minutes and then rinsing said fabrics with water. If said fabrics are to be washed, i.e., with a conventional composition comprising at least one surface active agent, said washing may be conducted before or after that said fabrics have been bleached.
• the present invention provides liquid bleaching compositions that may be applied neat onto a fabric to bleach, despite a standing prejudice against using bleach-containing compositions neat on fabrics while being safe to colors and fabrics perse.
• the bleaching pre-treatment operation may also be followed by the diluted bleaching process as described herein before either in bucket (hand operation) or in a washing machine.
• bleaching processes herein after said fabrics have been washed with a convention laundry detergent composition. Indeed, it has been observed that bleaching said fabrics with the compositions according to the present invention (typically diluted bleaching methods) after to washing them with a detergent composition provides superior whiteness and stain removal with less energy and detergent than if said fabrics are bleached first then washed.
• the present invention also encompasses a process of treating a hard-surface, as the inanimate surface.
• a composition, as defined herein, packaged in a UV light resistant container is contacted with the hard-surfaces to be treated.
• the present invention also encompasses a process of treating a hard-surface with a composition, as defined herein, wherein said process comprises the step of applying said composition to said hard-surface, preferably only soiled portions thereof, and optionally rinsing said hard-surface.
• composition as defined herein, may be applied to the surface to be treated in its neat form or in its diluted form typically up to 200 times their weight of water, preferably into 80 to 2 times their weight of water, and more preferably 60 to 2 times.
• compositions of the present invention are easy to rinse and provide good shine characteristics on the treated surfaces.
• hard-surfaces it is understood any hard-surfaces as mentioned herein before as well as dishes.
• compositions were made by mixing the listed ingredients in the listed proportions (weight % unless otherwise specified).
• Compositions (% weight) I II III IV V Akyposoft 100 NV® 0.5 0.5 - 0.3 0.4 Curox® 6 4 4 4.3 10 Trifluoromethylphenylketone 0.5 - - 0.3 - Acetoacetone - 0.4 - - 0.4 HEDP 0.1 0.05 0.16 0.1 - BHT 0.05 - - - 0.1 Propyl gallate - 0.1 - 0.05 - NaCl - - 0.1 0.5 - NaBr - - - - 1.0 Water and minors up to 100% Alkanizing agent up to pH 2 2.5 4 4 1.5
• Compositions (% weight) VI VII VIII IX X XI Akyposoft 100 NV® 0.5 0.5 0.5 0.2 0.2 - Curox® 5 7 10 10 6 9.5 Acetylacetone 0.5 0.5 0.5 - - - N,N
• compositions were packaged in a UV light resistant container, e.g., a white opaque thermoplastic bottle, like the package of Ace Candeggina® commercially available for instance in Italy. These compositions exhibit excellent bleaching performance as well as good stain removal performance when used to bleach fabrics or to treat a hard-surface, this both under neat and especially diluted conditions, even upon ageing of the composition, e.g. when used after 12 months storage at 20°C.

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• 1997
  • 1997-10-31 EP EP97870175A patent/EP0913462A1/de not_active Withdrawn
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  • 1998-10-30 AR ARP980105471 patent/AR012530A1/es unknown
  • 1998-11-02 WO PCT/US1998/023376 patent/WO1999023196A1/en active Application Filing
  • 1998-11-02 JP JP2000519056A patent/JP2001521982A/ja not_active Withdrawn
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