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
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/83—Mixtures of non-ionic with anionic 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
  • C11D1/825—Mixtures of compounds all of which are non-ionic
• • 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
  • C11D3/40—Dyes ; Pigments
  • C11D3/42—Brightening agents ; Blueing agents
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/60—Optical bleaching or brightening
  • D06L4/614—Optical bleaching or brightening in aqueous solvents
  • D06L4/621—Optical bleaching or brightening in aqueous solvents with anionic brighteners
• • 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
  • C11D1/02—Anionic compounds
  • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
  • C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
  • C11D1/146—Sulfuric acid esters
• • 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 relates to cleaning compositions. More particularly, the cleaning compositions according to the present invention are stable aqueous emulsions particularly suitable to be used in laundry applications for example as detergent compositions or as pre-wash treating compositions or as laundry additives to be used together with detergents.
• a great variety of cleaning compositions have been described in the art.
• a problem associated with common cleaning compositions is that they do not allow to deliver whitening performance which satisfactorily meet consumer's needs, when used in laundry application to treat different kind of fabrics, especially when used to treat synthetic fabrics such as polyesters, polyamides and the like.
• compositions suitable for use in laundry application whereby the whiteness to synthetic fabrics is improved. It is a further object of the present invention to provide such compositions which can be satisfactorily used for treating various types of fabrics and clean various types of stains while providing at the same time also good fabric safety to the fabrics treated therewith. Also said compositions should provide improved whitening performance to synthetic fabrics under most common wash conditions including conditions under which the wash temperature is low, i.e. below 60° C.
• aqueous compositions comprising a hydrophobic brightener wherein said hydrophobic brightener is emulsified in said compositions by a surfactant system comprising at least a hydrophobic surfactant having an HLB (Hydrophilic lipophilic balance) up to 9 and at least a hydrophilic surfactant having an HLB above 10.
• HLB Hydrophilic lipophilic balance
• compositions of the present invention allow to incorporate and to deliver hydrophobic brighteners into the wash solution, this under the most common wash conditions, e.g. below 60°C. Formulating such hydrophobic brighteners through liquid compositions being not emulsions or even through powder formulations does not allow to obtain the outstanding whitening performance associated with the present invention.
• hydrophobic brighteners also contribute to the multi-cycle whitening of cotton fabrics. Indeed, after several wash cycles cotton fibers assume a partially hydrophobic character due for example of deposition of organic species on the fabric surface, i.e. a hydrophobic layer of soils tend to form onto aged fabrics, and thus they become sensitive to hydrophobic brighteners.
• the hydrophobic brighteners may thus absorb onto said cotton fibers, adsorb UV light and retransmit visible blue light so providing superior whiteness.
• compositions of the present invention are that in addition to their outstanding whitening action said compositions allow also good stain removal.
• hydrophobic surfactants to emulsify said hydrophobic brighteners provides excellent hydrophobic soil removal and good grease cutting properties.
• a further advantage of the present invention is that it allows for great flexibility in formulating and provides compositions being chemically and physically stable and suitable to be used in the most efficient manner by the consumer.
• the preferred compositions therein comprise hydrogen peroxide.
• compositions provide a means to formulate ingredients with very low water solubility, without the need for using alcoholic or solvent mixtures, which are usually undesirable for aesthetic (odor) and toxicity reasons.
• Yet another advantage of the present invention is that hydrophobic brighteners, such as Tinopal SOP ® give to said compositions a perleascent color that improves the product aesthetics.
• EP-A-598973 discloses a composition comprising hydrogen peroxide and as a surfactant, a fully nonionic system, i.e. at least one nonionic with an HLB above 15, at least one nonionic with an HLB of from 13 to 15, at least one nonionic with an HLB of from 9 to 13 and at least one nonionic with an HLB below 9.
• This patent application further discloses the use of Tinopal CBS X® (4-4'-bis (2-2' styryl sulfonate) biphenyl) as an optical brightener.
• Tinopal CBS X® also named Brightener 49®
• Brightener 49® is a hydrophilic brightener having a solubility of 30 grams per liter at 25°C in deionized water.
• EP-A-598170 discloses emulsions of at least one hydrophobic nonionic surfactant and at least one hydrophilic nonionic surfactant, said emulsions further comprise hydrogen peroxide, or a source thereof.
• the invention disclosed in the '170 patent application allows to formulate compositions comprising H2O2 and a hydrophobic bleach activator (ATC), wherein said bleach activator is kept separate from H2O2.
• the pH of said emulsions is from 1 to 5.
• This patent application further discloses the use of optical brighteners as optional ingredients and mentions Brightener 49® in an example. Brightener 49® is not a brightener being almost insoluble in water, i.e. a hydrophobic brightener whose solubility in water is lower than 5 grams per liter at 25°C.
• the present invention is an aqueous emulsion comprising at least a hydrophilic surfactant having an HLB above 10 and at least a hydrophobic surfactant having an HLB up to 9, said aqueous emulsion further comprises a hydrophobic brightener whose solubility in water is lower than 5 grams per liter at 25 °C, or mixtures thereof.
• the present invention also encompasses a method of bleaching or washing fabrics, especially fabrics having a hydrophobic character such as synthetic fabrics to improve fabrics whiteness.
• the present invention also encompasses a process for the manufacture of said emulsions.
• compositions according to the present invention are stable aqueous emulsions of surfactants which further comprise a hydrophobic brightener whose solubility in water is lower than 5 grams per liter at 25°C.
• stable emulsion it is meant an emulsion which does not substantially separate into distinct layers, upon standing for at least two weeks at 50 °C.
• compositions of the present invention comprise a surfactant system of at least two different surfactants, i.e. at least a hydrophobic surfactant having an HLB up to 9 and at least a hydrophilic surfactant having an HLB above 10 in order to emulsify the hydrophobic brightener.
• said two different surfactants in order to form emulsions which are stable must have different HLB values (hydrophilic lipophilic balance), and preferably the difference in value of the HLBs of said two surfactants is at least 1, preferably at least 3.
• HLB values hydrophilic lipophilic balance
• Said surfactant system makes the compositions able to incorporate a hydrophobic brightener, i.e. a compound being almost insoluble in water medium, and to delivery it into the wash solution as a finely dispersed liquid.
• a hydrophobic brightener i.e. a compound being almost insoluble in water medium
• the present invention allows to exploit the benefits associated with a hydrophobic brightener otherwise not exploitable under common wash conditions, i.e. below 60°C, either through liquid or powder formulation.
• compositions according to the present invention comprise from 2% to 50% by weight of the total composition of said hydrophilic and hydrophobic surfactants, preferably from 5% to 40% and more preferably from 8% to 30%.
• compositions according to the present invention comprise at least from 0.1% by weight of the total composition of said hydrophobic surfactant, or mixtures thereof, preferably at least 3% and more preferably at least 5% and at least from 0.1% by weight of the total composition of said hydrophilic surfactant, or mixtures thereof, preferably at least 3% and more preferably at least 6%.
• hydrophobic nonionic surfactants and hydrophilic nonionic surfactants are the hydrophobic nonionic surfactants and hydrophilic nonionic surfactants.
• Said hydrophobic nonionic surfactants to be used herein have an HLB up to 9, preferably below 9, more preferably below 8 and said hydrophilic surfactants have an HLB above 10, preferably above 11, more preferably above 12.
• the hydrophobic nonionic surfactants to be used herein have excellent grease cutting properties, i.e. they have a solvent effect which contributes to hydrophobic soils removal.
• the hydrophobic surfactants act as carrier of the hydrophobic brighteners onto the fabrics allowing thereby said brighteners to work in close proximity with the fabrics surface since the beginning of the wash.
• Suitable nonionic surfactants for use herein include alkoxylated fatty alcohols preferably, fatty alcohol ethoxylates and/or propoxylates. Indeed, a great variety of such alkoxylated fatty alcohols are commercially available which have very different HLB values (hydrophilic lipophilic balance).
• HLB values of such alkoxylated nonionic surfactants depend essentially on the chain length of the fatty alcohol, the nature of the alkoxylation and the degree of alkoxylation. Hydrophilic nonionic surfactants tend to have a high degree of alkoxylation and a short chain fatty alcohol, while hydrophobic surfactants tend to have a low degree of alkoxylation and a long chain fatty alcohol.
• Surfactants catalogues are available which list a number of surfactants including nonionics, together with their respective HLB values.
• Suitable chemical processes for preparing the nonionic surfactants for use herein include condensation of corresponding alcohols with alkylene oxide, in the desired proportions. Such processes are well known to the man skilled in the art and have been extensively described in the art. As an alternative, a great variety of alkoxylated alcohols suitable for use herein is commercially available from various suppliers.
• Preferred hydrophobic nonionic surfactants to be used in the compositions according to the present invention are surfactants having an HLB up to 9 and being according to the formula RO-(C2H4O) n( C3H6O) m H, wherein R is a C6 to C22 alkyl chain or a C6 to C28 alkyl benzene chain, and wherein n+m is from 0.5 to 5 and n is from 0 to 5 and m is from 0 to 5 and preferably n+m is from 0.5 to 4 and, n and m are from 0 to 4.
• the preferred R chains for use herein are the C8 to C22 alkyl chains.
• Dobanol R 23-3 or Dobanol R 23-2, Lutensol R TO3, or mixtures thereof.
• These Dobanol R surfactants are commercially available from SHELL.
• These Lutensol R surfactants are commercially available from BASF and these Tergitol R surfactants are commercially available from UNION CARBIDE.
• hydrophobic nonionic surfactants to be used herein are non alkoxylated surfactants.
• An example is Dobanol 23 (HLB ⁇ 3 ).
• Preferred hydrophilic nonionic surfactants to be used in the compositions according to the present invention are surfactants having an HLB above 10 and being according to the formula RO-(C2H4O) n( C3H6O) m H, wherein R is a C6 to C22 alkyl chain or a C6 to C28 alkyl benzene chain, and wherein n+m is from 5 to 11 and n is from 0 to 11 and m is from 0 to 11, preferably n+m is from 6 to 10 and, n and m are from 0 to 10.
• n and m refer to the average degree of the ethoxylation/propoxylation.
• the preferred R chains for use herein are the C8 to C22 alkyl chains.
• hydrophilic surfactants may further be used in the present invention such as anionic surfactants, in particular sulfonate and sulfate surfactants.
• anionic surfactants are well-known in the art and have found wide application in commercial detergents.
• anionic surfactants include C8-C22 alkyl benzene sulfonates (LAS), C8-C22 alkyl sulfates (AS), unsaturated sulfates such as oleyl sulfate, C10-C18 alkyl alkoxy sulfates (AES) and C10-C18 alkyl alkoxy carboxylates.
• LAS C8-C22 alkyl benzene sulfonates
• AS C8-C22 alkyl sulfates
• unsaturated sulfates such as oleyl sulfate, C10-C18 alkyl alkoxy sulfates (AES) and C10-C18 alky
• the neutralizing cation for the anionic synthetic sulfonates and/or sulfates is represented by conventional cations which are widely used in detergent technology such as sodium, potassium or alkanolammonium.
• Preferred herein are the alkyl sulphate, or mixtures thereof, especially sodium alkyl sulphate having from 10 to 16 carbon atoms in the alkyl chain, preferably from 12 to 14.
• compositions according to the present invention may further comprise other surfactants which should however not significantly alter the weighted average HLB value of the overall composition.
• compositions according to the present invention comprise a hydrophobic brightener, or mixtures thereof.
• Brighteners are compounds which have the ability to fluorescent by absorbing ultraviolet wave-lengths of light and re-emitting visible light.
• Brighteners also referred to as fluorescent whitening agent (FWA)
• FWA fluorescent whitening agent
• Said brighteners are substituted stilbenes and biphenyls such as but not limited to polycyclic oxazole derivatives, styryl stilbene derivatives, aryltriazole derivatives, or mixtures thereof.
• hydrophobic brightener it is to be understood herein any brightener whose solubility in water is lower than 5 grams per liter at 25°C.
• Said hydrophobic brighteners to be used herein preferably have a solubility in water being lower than 3 and more preferably being lower than 1.
• solubility of a given compound it is to be understood herein the amount of said compound solubilized in deionized water at 25°C.
• a compound having a solubility being lower than 5 grams per liter means that when less than 5 grams of said given compound is incorporated in deionized water at 25°C said compound is entirely dissolved in said water, i.e. a clear and stable solution is obtained.
• incorporating 5 grams per liter or more of said given compound in water will result in a precipitation of said compound in said medium.
• compositions according to the present invention comprise from 0.02% to 1% by weight of the total composition of said hydrophobic brightener, preferably from 0.05% to 0.5% and more preferably from 0.05% to 0.2%.
• Preferred hydrophobic brighteners for use herein are styryl stilbene derivatives, or aryltriazole derivatives, or polycyclic oxazole derivatives such as benzo-oxazole derivatives, or mixtures thereof and particularly preferred herein are benzo-oxazole derivatives.
• An example of such a brightener is benzoxazole,2,2'- (thiophenaldyl)bis having the following formula C18H10N2O2S, commercially available from Ciba-Geigy under the trade name Tinopal SOP®. This brightener is almost insoluble in water, i.e. it has a solubility being lower than 1 gram per liter.
• compositions herein further comprise a hydrophilic brightener, or mixtures thereof.
• hydrophilic brightener it is to be understood herein any brightener whose solubility in water is higher than 10 grams per liter at 25°C.
• Said hydrophilic brighteners to be used herein preferably have a solubility in water being higher than 15 and more preferably being higher than 20.
• the compositions according to the present invention comprise from 0% to 1% by weight of the total composition of said hydrophilic brightener, preferably from 0% to 0.5% and more preferably from 0% to 0.2%.
• Such hydrophilic brighteners for use herein are the substituted stilbenes and biphenyls in general such as substituted stilbene 2,2'-disulfonic acid derivatives having a solubility in water higher than 10 grams per liter at 25°C.
• An example of such a brightener is 4-4'-bis (2-2' styryl sulfonate) biphenyl, commercially available from Ciba-Geigy under the trade name Brightener 49®.
• Other hydrophilic brighteners suitable to be used herein are for example Brightener 3® or Brightener 47®, also commercially available from Ciba-Geigy.
• compositions according to the present invention are aqueous. Accordingly, the compositions according to the present invention comprise from 10% to 95% by weight of the total composition of water, preferably from 30% to 90%, most preferably from 60% to 80%. Deionized water is preferably used.
• the pH of the formulation influences its stability.
• bleaching ingredients being optional but preferred ingredients of the compositions herein, it is of course necessary, for chemical stability purpose to formulate the compositions herein with bleaches at a pH as is of from 0 to 6, preferably of from 0.5 to 5 and more preferably from 0.5 to 4.
• the pH of the composition can be trimmed by all means available to the man skilled in the art.
• compositions according to the present invention comprise bleaches, i.e. hydrogen peroxide or a water-soluble source thereof.
• Suitable water-soluble sources of hydrogen peroxide include perborate, percarbonate, persilicate and persulphate salts.
• Hydrogen peroxide is most preferred to be used in the compositions according to the present invention.
• the compositions according to the present invention comprise from 0.5% to 20% by weight of the total composition of hydrogen peroxide, preferably from 2% to 15%, most preferably from 3% to 10%.
• compositions according to the present invention may further comprise a bleach activator.
• bleach activator it is meant herein any compound which reacts with hydrogen peroxide to form a peracid.
• hydrophobic bleach activators typically belong to the class of esters, amides, imides, or anhydrides.
• a particular family of bleach activators of interest in the present invention were disclosed in applicant's co-pending European patent application No 91870207.7. Particularly preferred in that family is acetyl triethyl citrate which was also disclosed in the context of bar soaps in FR 2 362 210. Acetyl triethyl citrate has the advantages that it is environmentally friendly as it eventually degrades into citric acid and alcohol.
• acetyl triethyl citrate has a good hydrolytical stability in the product upon storage and it is an efficient bleach activator.
• Other bleach activators to be used in the present invention are lactam derivatives. As used herein and unless otherwise specified, the term bleach activator includes mixtures of bleach activators.
• compositions according to the present invention may further comprise the usual optional ingredients such as perfumes, dyes, builders, chelants, pigments, enzymes, dye transfer inhibitors, solvents, buffering agents and the like.
• compositions comprise a hydrophobic brightener having a solubility in water being lower than 5 grams per liter, i.e. being almost insoluble in water
• the surfactant system to be chosen to emulsify said hydrophobic brightener depends on the HLB value of said brightener.
• a suitable way to proceed is to determine the HLB value of the hydrophobic ingredient (brightener), then select both the hydrophobic surfactants which have HLB values below said HLB value of said hydrophobic ingredient and the hydrophilic surfactants which have HLB values above said HLB value of said hydrophobic ingredient, wherein the difference in the HLB values of said hydrophobic and hydrophilic nonionic surfactants is at least 1, preferably at least 3.
• the emulsifying system meets the equation: where X refers to the hydrophobic ingredient to emulsify if several hydrophobic ingredients are present X refers to all of them, A refers to one of said nonionic surfactants (hydrophilic or hydrophobic), and B refers to the other said nonionic surfactant (hydrophilic or hydrophobic).
• an adequate nonionic surfactant system would comprise a hydrophobic nonionic surfactant with for instance an HLB of 6, such as a Dobanol R 23-2 and a hydrophilic nonionic surfactant with for instance an HLB of 15, such as a Dobanol R 91-10.
• compositions of the present invention allow to achieve improved whitening performance on hydrophobic-type of fabrics, i.e. synthetic fabrics such as polyesters, polyamides and the like.
• improved whitening performance it is meant herein that the whiteness on fabrics (synthetic) achieved by using a composition comprising a hydrophobic brightener emulsified by a surfactant system of at least one hydrophobic surfactant and at least one hydrophilic surfactant is improved, as compared to the whiteness obtained by using the same composition with a hydrophilic brightener instead of said hydrophobic one as herein defined.
• the hydrophobic brightener is delivered into the wash as a finely dispersed liquid and thus is active at low temperature used in common wash conditions (below 60°C).
• compositions of the present invention which further comprise a hydrophilic brightener as defined herein allow to achieve improved whitening performance on all kinds of fabrics (cotton natural fibers as well as synthetic and mixed fabrics) as compared to the same compositions comprising only said hydrophilic brightener as the brightener.
• compositions of the present invention comprising a hydrophobic brightener emulsified in a surfactant system as described herein is that said hydrophobic brightener may contribute to the multi-cycle whitening of cotton fibers even in absence of any hydrophilic brightener which are known to be particularly effective on cotton fabrics.
• Aged cotton fabrics become partially hydrophobic, i.e. they are covered by thin hydrophobic layers of soils such as deposition of organic materials thus becoming sensitive to hydrophobic brighteners.
• the present invention further encompasses a process for the manufacture of the composition described herein.
• the process according to the present invention comprises at least three steps: In the first step, a hydrophobic mixture is prepared which comprises at least said hydrophobic nonionic surfactant and hydrophobic brightener. Said hydrophobic mixture may further comprises other hydrophobic ingredients which are to be formulated in the composition, such as perfumes, solvents, enzymes, bleach activators and polymers.
• a hydrophilic mixture which comprises at least said water, and said hydrophilic nonionic surfactant.
• Said hydrophilic mixture preferably further comprises other hydrophilic ingredients which are to be formulated in the composition such as dyes, hydrophilic optical brighteners, builders, chelants, hydrogen peroxide and buffering agents.
• hydrogen peroxide when present is preferably added last, after said buffering agent has been added.
• said first and said second steps can be performed in any order, i.e. second step first is also suitable.
• said hydrophobic mixture and said hydrophilic mixture are mixed together.
• compositions according to the present invention are particularly useful as laundry detergent or as laundry pretreaters, i.e. compositions which are dispensed and left to act onto fabrics before they are washed, or as laundry additives to be used together with detergents to boost their performance.
• the compositions of the present invention may be incorporated per se in any type of detergents including detergents being in a liquid or a granular form.
• the technologies used to incorporate the compositions of the present invention in a detergent being in a granular form are those commonly known to those skilled in the art like spraying and/or encapsulation.
• the present invention further encompasses a method of bleaching and/or washing fabrics wherein a composition as defined hereinbefore is contacted with said fabrics. More specifically, in the preferred embodiment of the present invention where the compositions of the present invention comprise bleaches, the method of bleaching fabrics to improve fabric whiteness comprises the steps of first contacting said fabrics with a composition of the present invention, then allowing said fabrics to remain in contact with said composition, for a period of time sufficient to bleach said fabrics, typically 2 to 60 minutes, preferably 5 to 30 minutes, then rinsing said fabrics in water to remove said composition. If said fabrics are to be washed, i.e. with a conventional composition comprising at least one surface active agent, it is preferred to perform the method herein before said fabrics are washed.
• said method according to the present invention further comprises a subsequent step where said fabrics are washed with a detergent composition comprising at least one surface active agent.
• compositions are made which comprise the listed ingredients in the listed proportions (weight %).
• Compositions I II III IV Dobanol R 45-7 6 6 6 6
• Dobanol R 23-2 6 6 6 Hydrogen peroxide 7.5 7.5 7.5 7.5 Acetyl triethyl citrate 7.0 7.0 7.0 7.0 Brightener R 49 ---- ---- 0.1 0.1 Tinopal SOP R ---- 0.1 ---- 0.1 S,S-ethylene diamino disuccinic acid 0.1 0.1 0.1 0.1 0.1 0.1 Poly(4-vinylpyridine- N-oxyde) 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 Poly(4-vinylpyridine- N-oxyde) 0.1 0.1 0.1 0.1 0.1 HOES R 3639 0.2 0.2 0.2 0.2 0.2 Silicon 0.2 0.2 0.2 0.2 0.2 Deionized water --------------balance--------
• Composition I is an emulsion taken as reference in the following test and comprises no brighteners at all.
• compositions II and IV are representative of the present invention.
• Composition II is an emulsion of nonionic surfactants comprising among other hydrogen peroxide, a bleach activator (ATC) and a hydrophobic brightener, Tinopal SOP®.
• Composition IV differs from composition II in that it further comprises a hydrophilic brightener, Brightener 49®.
• Composition III is a composition representative of the prior art, i.e. an emulsion of nonionic surfactants comprising hydrogen peroxide and a bleach activator (ATC) and as a brightener a hydrophilic brightener.
• ATC bleach activator
• a single tracer launderometer test was carried out by using said bleaching compositions mentioned above followed by the use of a detergent composition.
• the test was performed in a stainless steel vessel. First 2 ml of each of the above bleaching compositions I to IV were diluted in 0.5 liters of tap water. The test was carried out at 18°C. The tracers, i.e. fabrics such as clothes, towels and the like, with standardized stains were added into the prepared solutions. The vessel was then kept under agitation for 20 minutes. At the end of the washing cycle the tracers were rinsed with water. Then, a detergent commercially available on the market (Dash Ultra®) was used to wash the tracers. 5g of the detergent were diluted into 0.5 liter of tap water. This solution was heated at 40°C. The vessel was then kept under agitation for 20 minutes with the tracers. At the end of the washing cycle the tracers were rinsed and dried. Then the tracers were evaluated by visual grading.
• the tracers i.e. fabrics such as clothes, towels and the like, with standardized stains were added into the prepared solutions. The vessel was then kept under
• compositions II and IV a hydrophobic brightener emulsified in a nonionic surfactant system
• composition III a composition available on the market comprising only a hydrophilic brightener as the brightener
• composition I* a hydrophilic brightener
• composition IV shows that the emulsions of the present invention comprising a hydrophobic and a hydrophilic brightener provide fabric whiteness improvement on various types of fabrics, polyester alone, cotton alone or mixtures thereof as compared to the compositions available on the market (see composition IV versus composition III).
• compositions according to the present invention are the following. These compositions are made comprising the listed ingredients in the listed proportions (weight %): Compositions I II III Dobanol R 45-7 6.7 6.0 6.0 Lutensol T03 8.3 --- ---- Na alkyl sulphate 2.0 --- ---- Dobanol R 23-2 ---- 6.0 6.0 Dobanol R 91-10 ---- 3.0 3.0 Hydrogen peroxide 7.5 7.5 7.5 Acetyl triethyl citrate 7.0 7.0 7.0 Brightener R 49 0.2 ---- ---- Brightener R 3 ---- 0.2 ---- Brightener R 47 ---- ---- 0.1 Tinopal SOP R 0.1 0.05 0.08 S,S-ethylene diamino disuccinic acid ---- 0.1 0.1 Diethylene triamine penta methylene phosphonic acid 1.0 --- ---- Poly(4-vinylpyridine-N-oxyde) 0.1 0.1 0.1 HOES R
• compositions I to III are each made by preparing two mixtures.
• a hydrophilic mixture is prepared which comprises the hydrophilic ingredients such as water, hydrophilic brightener, S,S-EDDS, poly(4-vinylpyridine-N-oxide), Dobanol R 45-7, Dobanol R 91-10, diethylene triamine penta methylene phosphonic acid or Na alkyl sulphate. Hydrogen peroxide is added in said hydrophilic mixture as last step.
• a hydrophobic mixture is prepared which comprises acetyl triethyl citrate, Dobanol R 23-2, Lutensol T03, hydrophobic brightener, silicone or Hoes R 3639. Then said hydrophobic mixture is poured into said hydrophilic mixture, while mixing.
• compositions according to the examples above are stable and provide excellent whitening performance and safety to the fabrics treated with them while being also efficient in removing stains. These advantages are observed when using said compositions as a laundry composition or as an additive or as a pre-bleach associated with a detergent composition.

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• Chemical & Material Sciences (AREA)
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• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Wood Science & Technology (AREA)
• Organic Chemistry (AREA)
• Textile Engineering (AREA)
• Detergent Compositions (AREA)
• Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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• 1994
  • 1994-06-10 DE DE69427905T patent/DE69427905T2/de not_active Expired - Fee Related
  • 1994-06-10 ES ES94201667T patent/ES2158878T3/es not_active Expired - Lifetime
  • 1994-06-10 EP EP94201667A patent/EP0686691B1/fr not_active Expired - Lifetime
• 1995
  • 1995-05-23 AU AU25551/95A patent/AU704895B2/en not_active Ceased
  • 1995-05-23 JP JP8502184A patent/JPH10501296A/ja active Pending
  • 1995-05-23 CA CA002191569A patent/CA2191569A1/fr not_active Abandoned
  • 1995-05-23 WO PCT/US1995/006482 patent/WO1995034621A1/fr active Application Filing
• 2001
  • 2001-08-09 GR GR20010401214T patent/GR3036360T3/el not_active IP Right Cessation

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