Patent Application
20060205624
The present invention relates to a composition comprising at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff, which produces in the CIElab colour coordinate system a relative hue angle of 220-320°, to a detergent composition, to a fabric softener composition as well as to a shading process using such a mixture.
A frequently employed method in bleaching and whitening is to use violet or blue dyes concurrently in order to improve the bleaching and whitening effect. If such a dye is used in conjunction with a fluorescent whitening agent, this can serve two different purposes. On the one hand, it is possible to try to achieve an increase in the degree of whiteness by compensating for the yellow of the fabric, in which case the white shade produced by the fluorescent whitening agent on the fabric is largely retained. On the other hand, the object can be to effect with the dye in question a change in the shade of the white effect produced by the fluorescent whitening agent on the fabric, in which case too an attempt is made additionally to achieve an increase in the degree of whiteness. It is thus possible to adjust the desired shade of the white effect.
Shading processes of materials such as paper and textile fabrics are known from e.g. DE 3125495.
These disclosed shading processes, respectively the disclosed mixtures of photocatalyst and dyestuff are not suitable for a regular use, such as in detergent or softener formulations, because the dyestuffs do accumulate with every use and after a few uses the fabrics are coloured.
Therefore, the goal of the present invention was to find a mixture of at least one photocatalyst and at least one azo and/or triphenylmethane dyestuff, which does not lead to a colouration of the fabric.
This problem was solved by a composition comprising at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff, which produces a relative hue angle of 220-320°, which is not light stable. That means that the components of the mixture, when applied to the fabric are destroyed by light.
Surprisingly, when the dyestuff as such (without the photocatalyst) is applied to the fabric, it is not destroyed (or destroyed much slower).
Therefore the present invention relates to a composition comprising at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff, which produce a relative hue angle of 220-320° and wherein the dyestuff component is degraded when the composition is exposed to light.
Colour coordinates and colour differences are expressed using the internationally standardized CIELAB tristimulus values:
This internationally accepted system has been developed by CIE (“Commission Internationale de I'Éclairage”). It is for example part of DIN 6174: 1979-01 as well as DIN 5033-3:1992-07.
Preferably the present invention relates to a composition comprising at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff, which produce a relative hue angle of 220-320° and wherein the dyestuff component is degraded when the composition is exposed to sunlight.
More preferably the present invention relates to a composition comprising at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff, which produce a relative hue angle of 220-320° and wherein the decrease rate of the azo dyestuff(s) and/or the triphenylmethane dyestuff(s) is at least 1% per 2 hours, preferably at least 2% when the composition is exposed to sunlight.
The degradation of the components can be determined spectrophotometrically.
Preferably, the photocatalyst is a phthalocyanine.
More preferably, the photocatalyst is a water-soluble phthalocyanine of Zn, Fe(II), Ca, Mg, Na, K, Al, Si(IV), P(V), Ti(IV), Ge(IV), Cr(VI), Ga(III), Zr(IV), In(III), Sn(IV) or Hf(VI);
Most preferably, the photocatalyst is a water-soluble phthalocyanine of the formula
or
in which
The number of substituents Q1 and Q2 in the formula (1a) and (1b) respectively, which may be identical or different, is between 1 and 8, and it is not imperative, as is generally the case with phthalocyanines, for it to be an integer (degree of substitution). If other noncationic substituents are present, the sum of the latter and the cationic substituents is between 1 and 4. The minimum number of substituents which must be present in the molecule is governed by the solubility of the resulting molecule in water. It is sufficiently soluble in water when enough of the phthalocyanine compound dissolves to effect a photodynamically catalysed oxidation on the fibre. A solubility as low as 0.01 mg/l may suffice, although one of from 0.001 to 1 g/l is generally advantageous.
Halogen means fluorine, bromine or, in particular, chlorine.
Especially suitable groups
are:
Preference is given to the group
Suitable heterocyclic rings in the group
are likewise the groups listed above, the bond to the other substituents merely being via a carbon atom.
In all of these substituents, phenyl, naphthyl and aromatic hetero rings may be substituted by one or two further radicals, for example by C1-C6alkyl, C1-C6alkoxy, halogen, carboxyl, carb-C1-C6alkoxy, hydroxyl, amino, cyano, sulfo, sulfonamido, etc.
Preference is given to a substituent from the group C1-C6alkyl, C1-C6alkoxy, halogen, carboxyl, carb-C1-C6alkoxy or hydroxyl.
Particularly suitable groups
are:
etc, wherein
All of the aforementioned nitrogen heterocycles can also be substituted by alkyl groups, either on a carbon atom or on another nitrogen atom in the ring. The alkyl group is preferably the methyl group.
A−s in formula (1a) is, as a counterion to the positive charge on the remainder of the molecule, any anion. In general, it is introduced by the preparation process (quaternization).
It is then preferably a halogen ion, an alkylsulfate or an arylsulfate ion. Arylsulfate ions which may be mentioned are the phenylsulfonate, p-tolylsulfonate and the p-chlorophenylsulfonate ion. The anion can however also be any other anion since the anions can be readily exchanged in a known manner; As− can thus also be a sulfate, sulfite, carbonate, phosphate, nitrate, acetate, oxalate, citrate, lactate ion or another anion of an organic carboxylic acid. The index s is the same as r for monovalent anions. For polyvalent anions, s has a value ≦r, in which case it must be chosen, depending on the conditions, such that it exactly balances the positive charge on the remainder of the molecule.
C1-C6alkyl and C1-C6alkoxy are straight-chain or branched alkyl or alkoxy radicals, such as, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, amyl, isoamyl, tert-amyl or hexyl or methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, amyloxy, isoamyloxy, tert-amyloxy or hexyloxy.
C2-C22alkenyl is, for example, allyl, methallyl, isopropenyl, 2-butenyl, 3-butenyl, isobutenyl, n-penta-2,4-dienyl, 3-methyl-but-2-enyl, n-oct-2-enyl, n-dodec-2-enyl, iso-dodecenyl, n-dodec-2-enyl or n-octadec-4-enyl.
Preferred photobleaching agents of the formula (1a) have the formula
in which
Other photobleaching agents which can be used according to the invention have the formula
in which
Very particularly preferred phthalocyanine compounds have the formula (4a),
in which
Other interesting phthalocyanine compounds which can be used according to the invention have the formula
in which
Further interesting phthalocyanine compounds which can be used according to the invention have the formula
in which
If the central atom Me in the phthalocyanine ring is Si(IV), the phthalocyanines used according to the invention may also have axial substituents (═R19) in addition to the substituents on the phenyl ring of the phthalocyanine ring. Such phthalocyanines have, for example, the formula
in which
Especially preferred phthalocyanine compounds are such compounds which are commercially available and used in washing agent compositions. Usually, the anionic phthalocyanine compounds are in the form of alkali metal salts, especially sodium salts.
Suitable azo dyes are for example such as described in U.S. Pat. No. 5,211,719 of formulae
wherein
Preferably, the azo dyestuffs are compounds of the following formulae
Preferably, the triphenylmethane dyestuffs are compounds of the following formulae:
A preferred embodiment of the present invention is a composition comprising
A more preferred embodiment of the present invention is a composition comprising at least one phthalocyanine compound of formula (1a), (1b), (2a), (3), (4), (4a), (5), (6) and/or (7), and
The composition, which comprises at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff, can be used in solid or liquid formulation.
A further embodiment is a solid formulation comprising a composition, which comprises at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff.
A preferred embodiment of the present invention is a solid formulation comprising at least one composition, which comprises
A more preferred embodiment of the present invention is a solid formulation comprising at least one composition, which comprises
A preferred embodiment of the present invention is a solid formulation comprising a composition, which comprises
Granulates are preferred as solid formulation.
The present invention also relates to granulates comprising
The sum of the wt-% of components a)-c) is always 100%.
The preferences for the phthalocyanines, for the azo and triphenylmethane dyestuffs as defined above also apply for the solid and/or granular formulation.
A preferred embodiment of the present invention relates to granulates comprising
A more preferred embodiment of the present invention relates to granulates comprising
The granulates according to the invention can be encapsulated or not
Encapsulating materials include especially water-soluble and water-dispersible polymers and waxes. Of those materials, preference is given to polyethylene glycols, polyamides, polyacrylamides, polyvinyl alcohols, polyvinylpyrrolidones, gelatin, hydrolysed polyvinyl acetates, copolymers of vinylpyrrolidone and vinyl acetate, and also polyacrylates, paraffins, fatty acids, copolymers of ethyl acrylate with methacrylate and methacrylic acid, and polymethacrylates.
The granulates according to the invention contain from 2 to 75 wt-%, preferably from 2 to 60 wt-%, especially from 5 to 55 wt-%, of component a), based on the total weight of the granulate.
The granulates in the formulations according to the invention contain from 10 to 95 wt-%, preferably from 10 to 85 wt-%, especially from 10 to 80 wt-%, of at least one further additive (component c)), based on the total weight of the granulate.
Such further additives may be anionic or non-ionic dispersing agents; water-soluble organic polymers; inorganic salt; low-molecular-weight organic acid or a salt thereof; wetting agents; disintegrants such as, for example, powdered or fibrous cellulose, microcrystalline cellulose; fillers such as, for example, dextrin; water-insoluble or water-soluble dyes or pigments; and also dissolution accelerators and optical brighteners. Aluminium silicates such as zeolites, and also compounds such as talc, kaolin, TiO2, SiO2 or magnesium trisilicate may also be used in small amounts.
The anionic dispersing agents used are, for example, the commercially available water-soluble anionic dispersing agents for dyes, pigments etc.
The following products, especially, come into consideration: condensation products of aromatic sulfonic acids and formaldehyde, condensation products of aromatic sulfonic acids with unsubstituted or chlorinated biphenyls or biphenyl oxides and optionally formaldehyde, (mono-/di-)alkylnaphthalenesulfonates, sodium salts of polymerised organic sulfonic acids, sodium salts of polymerised alkylnaphthalenesulfonic acids, sodium salts of polymerised alkylbenzenesulfonic acids, alkylarylsulfonates, sodium salts of alkyl polyglycol ether sulfates, polyalkylated polynuclear arylsulfonates, methylene-linked condensation products of arylsulfonic acids and hydroxyarylsulfonic acids, sodium salts of dialkylsulfosuccinic acids, sodium salts of alkyl diglycol ether sulfates, sodium salts of polynaphthalene-methanesulfonates, ligno- or oxyligno-sulfonates or heterocyclic polysulfonic acids.
Especially suitable anionic dispersing agents are condensation products of naphthalene-sulfonic acids with formaldehyde, sodium salts of polymerised organic sulfonic acids, (mono-/di-)alkylnaphthalenesulfonates, polyalkylated polynuclear arylsulfonates, sodium salts of polymerised alkylbenzenesulfonic acid, lignosulfonates, oxylignosulfonates and condensation products of naphthalenesulfonic acid with a polychloromethylbiphenyl.
Suitable non-ionic dispersants are especially compounds having a melting point of, preferably, at least 35° C. that are emulsifiable, dispersible or soluble, for example the following compounds:
Especially suitable non-ionic dispersants are surfactants of formula
R20—O-(alkylene-O)n—R21 (8),
wherein
The substituents R20 and R21, in formula (8) are advantageously each the hydrocarbon radical of an unsaturated or, preferably, saturated aliphatic monoalcohol having from 8 to 22 carbon atoms. The hydrocarbon radical may be straight-chain or branched. R20 and R21 are preferably each independently of the other an alkyl radical having from 9 to 14 carbon atoms.
Aliphatic saturated monoalcohols that come into consideration include natural alcohols, e.g. lauryl alcohol, myristyl alcohol, cetyl alcohol or stearyl alcohol, and also synthetic alcohols, e.g. 2-ethylhexanol, 1,1,3,3-tetramethylbutanol, octan-2-ol, isononyl alcohol, trimethylhexanol, trimethylnonyl alcohol, decanol, C9-C11oxo-alcohol, tridecyl alcohol, isotridecyl alcohol and linear primary alcohols (Alfols) having from 8 to 22 carbon atoms. Some examples of such Alfols are Alfol (8-10), Alfol (9-11), Alfol (10-14), Alfol (12-13) and Alfol (16-18). (“Alfol” is a registered trade mark).
Unsaturated aliphatic monoalcohols are, for example, dodecenyl alcohol, hexadecenyl alcohol and oleyl alcohol.
The alcohol radicals may be present singly or in the form of mixtures of two or more components, e.g. mixtures of alkyl and/or alkenyl groups that are derived from soybean fatty acids, palm kernel fatty acids or tallow oils.
(Alkylene-O) chains are preferably divalent radicals of the formulae
and
Examples of a cycloaliphatic radical are cycloheptyl, cyclooctyl and preferably cyclohexyl. As non-ionic dispersants there come into consideration preferably surfactants of formula
wherein
Further important non-ionic dispersants correspond to formula
wherein
The non-ionic dispersants of formulae (8) to (10) can also be used in the form of mixtures.
For example, as surfactant mixtures there come into consideration non-end-group-terminated fatty alcohol ethoxylates of formula (8), e.g. compounds of formula (8) wherein
Examples of non-ionic dispersants of formulae (8), (9) and (10) include reaction products of a C10-C13fatty alcohol, e.g. a C13oxo-alcohol, with from 3 to 10 mol of ethylene oxide, propylene oxide and/or butylene oxide or the reaction product of one mol of a C13fatty alcohol with 6 mol of ethylene oxide and 1 mol of butylene oxide, it being possible for the addition products each to be end-group-terminated with C1-C4alkyl, preferably methyl or butyl.
Such dispersants can be used singly or in the form of mixtures of two or more dispersants.
Instead of or in addition to the dispersing agent or agents, the granulates according to the invention may comprise a water-soluble organic polymer, which may also have dispersing properties. Such polymers may be used singly or as mixtures of two or more polymers. As water-soluble polymers (which may, but need not, have film-forming properties), there come into consideration, for example, gelatins, polyacrylates, polymethacrylates, copolymers of ethyl acrylate, methyl methacrylate and methacrylic acid (ammonium salt), polyvinylpyrrolidones, vinylpyrrolidones, vinyl acetates, copolymers of vinylpyrrolidone with long-chain olefins, poly(vinylpyrrolidone/dimethylaminoethyl methacrylates), copolymers of vinylpyrrolidone/dimethylaminopropyl methacrylamides, copolymers of vinylpyrrolidone/dimethylaminopropyl acrylamides, quaternised copolymers of vinylpyrrolidones and dimethylaminoethyl methacrylates, terpolymers of vinylcaprolactam/vinylpyrrolidone/dimethylaminoethyl methacrylates, copolymers of vinylpyrrolidone and methacrylamidopropyltrimethylammonium chloride, terpolymers of caprolactam/vinylpyrrolidone/dimethylaminoethyl methacrylates, copolymers of styrene and acrylic acid, polycarboxylic acids, polyacrylamides, carboxymethyl cellulose, hydroxymethyl cellulose, polyvinyl alcohols, hydrolysed and non-hydrolysed polyvinyl acetate, copolymers of maleic add with unsaturated hydrocarbons and also mixed polymerisation products of the mentioned polymers. Further suitable substances are polyethylene glycol (MW=2000-20 000), copolymers of ethylene oxide with propylene oxide (MW>3500), condensation products (block polymerisation products) of alkylene oxide, especially propylene oxide, copolymers of vinylpyrrolidone with vinyl acetate, ethylene oxide-propylene oxide addition products with diamines, especially ethylenediamine, polystyrenesulfonic acid, polyethylenesulfonic acid, copolymers of acrylic acid with sulfonated styrenes, gum arabic, hydroxypropyl methylcellulose, sodium carboxymethyl cellulose, hydroxypropyl methylcellulose phthalate, maltodextrin, starch, sucrose, lactose, enzymatically modified and subsequently hydrated sugars, as are obtainable under the name “Isomalt”, cane sugar, polyaspartic acid and tragacanth.
Among those water-soluble organic polymers, special preference is given to carboxymethyl cellulose, polyacrylamides, polyvinyl alcohols, polyvinylpyrrolidones, gelatins, hydrolysed polyvinyl acetates, copolymers of vinylpyrrolidone and vinyl acetate, maltodextrins, polyaspartic acid and also polyacrylates and polymethacrylates.
For use as inorganic salts there come into consideration carbonates, hydrogen carbonates, phosphates, polyphosphates, sulfates, silicates, sulfites, borates, halides and pyrophosphates, preferably in the form of alkali metal salts. Preference is given to water-soluble salts such as, for example, alkali metal chlorides, alkali phosphates, alkali carbonates, alkali polyphosphates and alkali sulfates and water-soluble salts used in washing agent and/or washing agent additive formulations.
There come into consideration as low-molecular-weight acids, for example, mono- or polycarboxylic acids. Of special interest are aliphatic carboxylic acids, especially those having a total number of from 1 to 12 carbon atoms. Preferred acids are aliphatic C1-C12-mono- or -poly-carboxylic acids, the monocarboxylic acids being especially those having at least 3 carbon atoms in total. As substituents of the carboxylic acids there come into consideration, for example, hydroxy and amino, especially hydroxy. Special preference is given to aliphatic C2-C12polycarboxylic acids, especially aliphatic C2-C6polycarboxylic acids. Very special preference is given to hydroxy-substituted aliphatic C2-C6polycarboxylic acids. These compounds may be used in the form of the free acid or a salt, especially an alkali salt.
There may also be used aminopolycarboxylates (e.g. sodium ethylenediaminetetraacetate), phytates, phosphonates, aminopolyphosphonates (e.g. sodium ethylenediaminetetraphosphonate), aminoalkylenepoly(alkylenephosphonates), polyphosphonates, polycarboxylates or water-soluble polysiloxanes.
As examples of low-molecular-weight organic acids and salts thereof there may be mentioned oxalic acid, tartaric acid, acetic acid, propionic acid, succinic acid, maleic acid, citric acid, formic acid, gluconic acid, p-toluenesulfonic acid, terephthalic acid, benzoic acid, phthalic acid, acrylic acid and polyacrylic acid.
The optical brighteners may be selected from a wide range of chemical types such as 4,4′-bis-(triazinylamino)-stilbene-2,2′-disulfonic acids, 4,4′-bis-(triazol-2-yl)stilbene-2,2′-disulfonic acids, 4,4′-(diphenyl)-stilbenes, 4,4′-distyryl-biphenyls, 4-phenyl-4′-benzoxazolyl-stilbenes, stilbenyl-naphthotriazoles, 4-styryl-stilbenes, bis-(benzoxazol-2-yl) derivatives, bis-(benzimidazol-2-yl) derivatives, coumarines, pyrazolines, naphthalimides, triazinyl-pyrenes, 2-styryl-benzoxazole- or -naphthoxazole derivatives, benzimidazole-benzofuran derivatives or oxanilide derivatives.
With particular reference to the use of a composition, which is an aqueous textile finishing composition, preferred 4,4′-bis-(triazinylamino)-stilbene-2,2′-disulfonic acids are those having the formula (11):
in which
Especially preferred compounds of formula (11) are those in which each R26 is 2,5-disulfophenyl and each R27 is morpholino; or each R26 is 2,5-disulfophenyl and each R27 is N(C2H5)2; or each R26 is 3-sulfophenyl and each R27 is NH(CH2CH2OH) or N(CH2CH2OH)2; or each R26 is 4-sulfophenyl and each R27 is N(CH2CH2OH)2; and, in each case, the sulfo group is SO3M in which M is sodium.
Preferred 4,4′-bis-(triazol-2-yl)stilbene-2,2′-disulfonic acids are those having the formula (12):
in which
Especially preferred compounds of formula (12) are those in which R28 is phenyl, R29 is H and M is sodium.
One preferred 4,4′-(diphenyl)-stilbene is that having the formula (13):
Preferably, 4,4′-distyryl-biphenyls used are those of formula (14):
in which
Especially preferred compounds of formula (14) are those in which n is 1 and each R30 is a 2-SO3M group in which M is sodium and each R31 is H, or each R31 is —O(CH2)3N(+)(CH3)2An(−) in which An(−) is acetate.
Preferred 4-phenyl-4′-benzoxazolyl-stilbenes have the formula (15):
in which
An especially preferred compound of formula (15) is that in which R32 is 4-CH3 and R33 is 2-CH3.
Preferably, stilbenyl-naphthotriazoles used are those of formula (16):
in which
Especially preferred compounds of formula (16) are those in which R34 and R35 are H and R36 is 2-SO3M in which M is Na.
Preferably, 4-styryl-stilbenes used are those of formula:
in which
Especially preferred compounds of formula (17) are those in which each of R37 and R38 is 2-cyano; 2-SO3M in which M is sodium or O(CH2)3N(+)(CH3)2An(−) in which An(−) is acetate.
Preferred bis-(benzoxazol-2-yl) derivatives are those of formula (18):
in which
Especially preferred compounds of formula (18) are those in which each R39 is H and X is
or one group R39 in each ring is 2-methyl and the other R39 is H and X is —CH═CH—; or one group R39 in each ring is 2-C(CH3)3 and the other R39 is H and X is
Preferred bis-(benzimidazol-2-yl) derivatives are those of formula (19):
in which
Especially preferred compounds of formula (19) are those in which R40 and R41, are each H, R42 is SO3M in which M is sodium and X1 is —CH═CH—.
Preferred coumarines are those of formula:
in which
Especially preferred compounds of formula (20) are those having the formula (21) and (22):
Preferably, pyrazolines used are those having the formula (23):
in which
Preferred naphthalimides are those of formula (26):
in which R52 is C1-C4-alkyl or —CH2CH2CH2N(+)(CH3)3;
Especially preferred compounds of formula (26) are those having the formula (27) and (28):
Preferred triazinyl-pyrenes used are those of formula (29):
in which
Especially preferred compounds of formula (29) are those in which each R55 is methoxy.
Preferred 2-styryl-benzoxazole- or -naphthoxazole derivatives are those having the formula (30):
in which
Especially preferred compounds of formula (30) are those in which R56 is a 4-phenyl group and each of R57 to R60 is H.
Preferred benzimidazole-benzofuran derivatives are those having the formula (31):
in which
A particularly preferred compound of formula (31) is that in which R61 is methoxy, R62 and R63 are each methyl and An(−) is methane sulfonate.
Preferred oxanilide derivatives include those having the formula (32):
in which
Preferred FWA are those having one of the formulae:
in which
In the compounds of formulae (33) to (40), C1-C4-alkyl groups are, e.g., methyl, ethyl, n-propyl, isopropyl and n-butyl, especially methyl. Aryl groups are naphthyl or, especially, phenyl.
Specific examples of preferred compounds of formula (33) are those having the formulae:
Specific preferred examples of compounds of formula (34) are those of formulae:
in which n has its previous significance.
Preferred examples of compounds of formula (36) are those having the formulae:
Preferred examples of compounds of formula (37) are those of formulae:
A preferred example of a compound of formula (40) is that having the formula (57):
The compounds of formulae (23) to (57) are known and may be obtained by known methods.
Further preferred FWA's are those of the class of cationic bistyrylphenyl fluorescent whitening agent having the formula (58):
in which
Preferred compounds of formula (58) are those in which Y is 1,4-phenylene or 4,4′-diphenylene; R80 is hydrogen; methyl or cyano; R81 and R82 are each methyl or cyano; and R83 and An(−) have their previously indicated preferred meanings.
One particularly preferred compound of formula (58) is that having the formula (59):
The compounds of formula (58) and their production are described in U.S. Pat. No. 4,009,193.
A further preferred class of cationic bistyrylphenyl fluorescent whitening agent is that having the formula (60):
in which
Preferred compounds of formula (60) are those in which q is 1; R80 is hydrogen, chlorine, C1-C4-alkyl or C1-C4-alkoxy; Y1 is (CH2)2; R84 and R85 are the same and each is methyl or ethyl; R86 is methyl or ethyl; p is 1; and An(−) is CH3OSO3 or C2H5OSO3.
The compounds of formula (60) and their production are described in U.S. Pat. No. 4,339,393.
A further preferred class of cationic bistyrylphenyl fluorescent whitening agent is that having the formula (61):
in which R80, Y1, An(−), p and q have their previous significance,
Preferred compounds of formula (61) are those in which R80 is hydrogen; chloro; C1-C4-alkyl or C1-C4-alkoxy; R87 and R88, independently of one another, are C1-C4-alkyl or, together with the nitrogen atom to which they are attached, form a pyrrolidine, piperidine or morpholine ring; R89 is hydrogen; C1-C4-alkyl or C3-C4-alkenyl or R87, R88 and R89, together with the nitrogen atom to which they are attached, form a pyridine ring; and Z is sulfur, —SO2— or —SO2NH—.
The compounds of formula (61) and their production are described in U.S. Pat. No. 4,486,352.
A further preferred class of cationic bistyrylphenyl fluorescent whitening agent is that having the formula (62):
in which R80, R87, R88, R89, Y1, An(−), p and q have their previous significance.
Preferred compounds of formula (62) are those in which q is 1; R80 is hydrogen; chloro; C1-C4-alkyl or C1-C4-alkoxy; R87 and R88, independently of one another, are C1-C4-alkyl or R87 and R88 together with the nitrogen atom to which they are attached, form a pyrrolidine; piperidine or morpholine ring; R89 is hydrogen; C1-C4-alkyl or C3-C4-alkenyl or R87, R88 and R89, together with the nitrogen atom to which they are attached, form a pyridine ring.
The compounds of formula (62) and their production are described in U.S. Pat. No. 4,602,087.
One preferred class of amphoteric styrene fluorescent whitening agent is that having the formula (63):
in which R80, R87, R88, Y1 and q have their previous significance and
Preferred compounds of formula (63) are those in which Z1 is oxygen; a direct bond; —CONH—; —SO2NH— or —COO—; especially oxygen; q is 1; R80 is hydrogen; C1-C4-alkyl; methoxy or chlorine; and R87, R88, Y1 and Q have their previous significance.
The compounds of formula (63) and their production are described in U.S. Pat. No. 4,478,598.
One preferred class of amine oxide fluorescent whitening agent is that having the formula:
in which
Preferred brightener radicals B are those having the formula:
in which
Preferably Z2 is oxygen; —SO2— or —SO2N(R94)— in which R94 is hydrogen or C1-C4-alkyl optionally substituted by hydroxyl, halogen or cyano; and R91 and R92, independently of one another, are C1-C4-alkyl optionally substituted by halogen, cyano, hydroxyl, C1-C4-alkoxy, phenyl, chlorophenyl, methylphenyl, methoxyphenyl or C2-C5-alkoxycarbonyl. Other preferred compounds of formula (62) are those in which Z2 is oxygen; sulfur, —SO2—; —CON(R94)— or —SO2N(R94)— in which R94 is hydrogen or C1-C4-alkyl optionally substituted by hydroxyl, halogen or cyano; and Y2 is C1-C4-alkylene.
The compounds of formula (64) and their production are described in U.S. Pat. No. 4,539,161.
One preferred class of cationic phosphinic acid salt fluorescent whitening agent is that having the formula (65):
in which
Preferably, brightener radical B1 has the formula:
or the formula:
each optionally substituted by one to four substituents selected from halogen, C1-C4-alkyl, C1-C4-hydroxyalkyl, C1-C4-halogenoalkyl, C1-C4-cyanoalkyl, C1-C4-alkoxy-C1-C4-alkyl, phenyl-C1-C4-alkyl, carboxy-C1-C4-alkyl, carb-C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkenyl, C5-C8-cycloalkyl, C1-C4-alkoxy, C1-C4-alkenoxy, C1-C4-alkoxycarbonyl, carbamoyl, cyano, C1-C4-alkyl-sulfonyl, phenylsulfonyl, C1-C4-alkoxysulfonyl, sulfamoyl, hydroxyl, carboxyl, sulfo and trifluoromethyl.
The compounds of formula (65) and their production are described in GB-A-2 023 605.
Preferred bis(triazinyl)diaminostilbene anionic fluorescent whitening agents for use in the present invention are those having the formula (66):
Preferred dibenzofuranylbiphenyl anionic fluorescent whitening agents for use in the present invention are those having the formula (67):
Preferred anionic bistyrylphenyl fluorescent whitening agents for use in the present invention are those having the formula (68):
In the formulae (66) to (68),
The compounds of formulae (66) to (68) are known and may be obtained by known methods.
Especially preferred are the non-ionic or the anionic FWA's.
The granulates in the formulations according to the invention may contain from 0 to 15 wt-% water (component c), based on the total weight of the granulate.
The granulates in the formulations according to the invention preferably have an average particle size of <500 μm. Greater preference is given to the particle size of the granulates being from 40 to 400 μm.
A preferred embodiment of the present invention relates to granulates comprising
A more preferred embodiment of the present invention relates to granulates comprising
A further embodiment is a liquid formulation comprising a composition comprising at least one photocatalyst and at least one azo dyestuff and/or at least one triphenylmethane dyestuff.
Preferably a liquid formulation comprising
More preferably a liquid formulation comprising
Especially preferred is a liquid formulation comprising
The preferences for the phthalocyanines, for the azo and triphenylmethane dyestuffs as defined above also apply for the liquid formulation.
As organic solvents, polar solvents are preferred. Especially preferred are C1-C4-alcohols or water.
If appropriate, the liquid formulation according to the invention can further comprise optional additives; examples are preservatives or mixtures of preservatives, such as chloroacetamide, triazine derivates, benzoisothiazolines, 2-methyl-2H-isothiazol-3on, 2-octyl-2H-isothiazol-3on, 2-brom-2-nitropropan-1,3-diol or aqueous formaldehyde solution; Mg/Al silicates or mixtures of Mg/Al silicates, such as bentonite, montmorillonite, zeolites or highly disperse silicic acids; odour improvers and perfuming agent or mixtures thereof, antifoam agents or mixtures thereof; builders or mixtures thereof; protective colloids or mixtures thereof; stabilizers or mixtures thereof; sequestering agents and antifreeze agents or mixtures thereof, such as propylene glycol.
A preferred embodiment of the present invention related to a liquid formulation comprising
A more preferred embodiment of the present invention related to a liquid formulation comprising
The composition according to the invention is used especially in a washing or softener formulation. Such a washing or softener formulation may be in solid, liquid, gel-like or paste-like form, for example in the form of a liquid, non-aqueous washing agent composition containing not more than 5 wt-%, preferably from 0 to 1 wt-%, water and based on a suspension of a builder substance in a non-ionic surfactant, for example as described in GB-A-2 158 454.
The washing formulations may also be in the form of powders or (super-)compact powders, in the form of single- or multi-layer tablets (tabs), in the form of washing agent bars, washing agent blocks, washing agent sheets, washing agent pastes or washing agent gels, or in the form of powders, pastes, gels or liquids used in capsules or in pouches (sachets).
However, the washing agent compositions are preferably in the form of non-aqueous formulations, powders, tabs or granules.
The present invention accordingly relates also to washing agent formulations containing
The sum of the wt-% of components I)-VI) in a formulation is always 100%.
All the preferences mentioned hereinbefore apply to the granulate E).
The present invention accordingly relates also to washing agent formulations containing
The percentages of components I) to VI) in the washing agent formulations herein below are in all cases based on the total weight of the washing agent formulation.
The anionic surfactant A) can be, for example, a sulfate, sulfonate or carboxylate surfactant or a mixture thereof. Preferred sulfates are those having from 12 to 22 carbon atoms in the alkyl radical, optionally in combination with alkyl ethoxysulfates in which the alkyl radical has from 10 to 20 carbon atoms.
Preferred sulfonates are e.g. alkylbenzenesulfonates having from 9 to 15 carbon atoms in the alkyl radical. The cation in the case of anionic surfactants is preferably an alkali metal cation, especially sodium.
The anionic surfactant component may be, e.g., an alkylbenzenesulfonate, an alkylsulfate, an alkylethersulfate, an olefinsulfonate, an alkanesulfonate, a fatty acid salt, an alkyl or alkenyl ether carboxylate or an a-sulfofatty acid salt or an ester thereof. Preferred are alkylbenzenesulfonates having 10 to 20 carbon atoms in the alkyl group, alkylsulfates having 8 to 18 carbon atoms, alkylethersulfates having 8 to 22 carbon atoms, and fatty acid salts being derived from palm oil or tallow and having 8 to 22 carbon atoms. The average molar number of ethylene oxide added in the alkylethersulfate is preferably 1 to 22, preferably 1 to 10. The salts are preferably derived from an alkaline metal like sodium and potassium, especially sodium. Highly preferred carboxylates are alkali metal sarcosinates of formula
R—CO(R1)CH2COOM1 in which R is alkyl or alkenyl having 8-20 carbon atoms in the alkyl or alkenyl radical, R1 is C1-C4 alkyl and M1 is an alkali metal, especially sodium.
The nonionic surfactant component may be, e.g., primary and secondary alcohol ethoxylates, especially the C8-C20 aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol, and more especially the C10-C15 primary and secondary aliphatic alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol. Non-ethoxylated nonionic surfactants include alkylpolyglycosides, glycerol monoethers, and polyhydroxyamides (glucamide).
The total amount of anionic surfactant and nonionic surfactant is preferably 5-50 wt-%, preferably 5-40 wt-% and more preferably 5-30 wt-%. As to these surfactants it is preferred that the lower limit is 10 wt-%.
Preferred carboxylates are alkali metal sarcosinates of formula R19—CO—N(R20)—CH2COOM′1 wherein R19 is alkyl or alkenyl having from 8 to 20 carbon atoms in the alkyl or alkenyl radical, R20 is C1-C4alkyl and M′1 is an alkali metal.
The non-ionic surfactant B) can be, for example, a condensation product of from 3 to 8 mol of ethylene oxide with 1 mol of a primary alcohol having from 9 to 15 carbon atoms.
As builder substance C) there come into consideration, for example, alkali metal phosphates, especially tripolyphosphates, carbonates or hydrogen carbonates, especially their sodium salts, silicates, aluminosilicates, polycarboxylates, polycarboxylic acids, organic phosphonates, aminoalkylenepoly(alkylenephosphonates) or mixtures of those compounds.
Especially suitable silicates are sodium salts of crystalline layered silicates of the formula NaHSitO2t+1.pH2O or Na2SitO2t+1.pH2O wherein t is a number from 1.9 to 4 and p is a number from 0 to 20.
Among the aluminosilicates, preference is given to those commercially available under the names zeolithe A, B, X and HS, and also to mixtures comprising two or more of those components. Zeolithe A is preferred.
Among the polycarboxylates, preference is given to polyhydroxycarboxylates, especially citrates, and acrylates and also copolymers thereof with maleic anhydride. Preferred polycarboxylic acids are nitrilotriacetic acid, ethylenediaminetetraacetic acid and ethylenediamine disuccinate either in racemic form or in the enantiomerically pure (S,S) form.
Phosphonates or aminoalkylenepoly(alkylenephosphonates) that are especially suitable are alkali metal salts of 1-hydroxyethane-1,1-diphosphonic acid, nitrilotris(methylenephosphonic acid), ethylenediaminetetramethylenephosphonic acid, hexamethylenediamin N,N,N′,N′ tetrakis methanphosphonic acid and diethylenetriaminepentamethylenephosphonic acid, as well as the salts therefrom.
Suitable peroxide components include, for example, the organic and inorganic peroxides (like sodium peroxides) known in the literature and available commercially that bleach textile materials at conventional washing temperatures, for example at from 5 to 95° C.
In particular, the organic peroxides are, for example, monoperoxides or polyperoxides having alkyl chains of at least 3, preferably 6 to 20, carbon atoms; in particular diperoxydicarboxylates having 6 to 12 C atoms, such as diperoxyperacetates, diperoxypersebacates, diperoxyphthalates and/or diperoxydodecanedioates, especially their corresponding free acids, are of interest
Especially preferred are mono- oder polyperoxide, especially organic peracids or their salts such as phthalimidoperoxycapronic acid, peroxybenzoic acid, diperoxydodecandiacid, diperoxynonandiacid, diperoxydecandiacid, diperoxyphthalic acid or their salts.
The amount of peroxide is preferably 0.5-30 wt-%, preferably 1-20 wt-% and more preferably 1-15 wt-%. In case a peroxide is used, the lower limit is preferably 2 wt-%, especially 5 wt-%.
Preferably, however, inorganic peroxides are used, for example persulfates, perborates, percarbonates and/or persilicates. It will be understood that mixtures of inorganic and/or organic peroxides can also be used. The peroxides may be in a variety of crystalline forms and have different water contents, and they may also be used together with other inorganic or organic compounds in order to improve their storage stability.
The peroxides are added to the agent preferably by mixing the components, for example using a screw metering system and/or a fluidised bed mixer.
The agents may comprise, in addition to the combination according to the invention, one or more optical brighteners, for example from the class bis-triazinylamino-stilbenedisulfonic acid, bis-triazolyl-stilbenedisulfonic acid, bis-styryl-biphenyl or bis-benzofuranylbiphenyl, a bis-benzoxalyl derivative, bis-benzimidazolyl derivative or coumarin derivative or a pyrazoline derivative.
The detergents used will usually contain one or more auxiliaries such as soil suspending agents, for example sodium carboxymethylcellulose; salts for adjusting the pH, for example alkali or alkaline earth metal silicates; foam regulators, for example soap; salts for adjusting the spray drying and granulating properties, for example sodium sulphate; perfumes; and also, if appropriate, antistatic and softening agents; such as smectite clays; photobleaching agents; pigments; and/or shading agents. These constituents should, of course, be stable to any bleaching system employed. Such auxiliaries can be present in an amount of, for example, 0.1 to 20 wt-%, preferably 0.5 to 10 wt-%, especially 0.5 to 5 wt-%, based on the total weight of the detergent
Furthermore, the detergent can optionally contain enzymes. Enzymes can be added to detergents for stain removal. The enzymes usually improve the performance on stains that are either protein- or starch-based, such as those caused by blood, milk, grass or fruit juices. Preferred enzymes are cellulases, proteases, amylases and lipases. Preferred enzymes are cellulases and proteases, especially proteases. Cellulases are enzymes which act on cellulose and its derivatives and hydrolyze them into glucose, cellobiose, cellooligosaccharide. Cellulases remove dirt and have the effect of mitigating the roughness to the touch. Examples of enzymes to be used include, but are by no means limited to, the following:
The enzymes can optionally be present in the detergent. When used, the enzymes are usually present in an amount of 0.01-5 wt-%, preferably 0.05-5 wt-% and more preferably 0.1-4 wt-%, based on the total weight of the detergent.
In addition to the bleach catalyst according to formula (1) it is also possible to use further transition metal salts or complexes known as bleach-activating active ingredients and/or conventional bleach activators, that is to say compounds that, under perhydrolysis conditions, yield unsubstituted or substituted perbenzo- and/or peroxo-carboxylic acids having from 1 to 10 carbon atoms, especially from 2 to 4 carbon atoms. Suitable bleach activators include the customary bleach activators, mentioned at the beginning, that carry O- and/or N-acyl groups having the indicated number of carbon atoms and/or unsubstituted or substituted benzoyl groups. Preference is given to polyacylated alkylenediamines, especially tetraacetylethylenediamine (TAED), acylated glycolurils, especially tetraacetylglycoluril (TAGU), N,N-diacetyl-N,N-dimethylurea (DDU), acylated triazine derivatives, especially 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), compounds of formula:
wherein R26 is a sulfonate group, a carboxylic acid group or a carboxylate group, and wherein R27 is linear or branched (C7-C15)alkyl, especially activators known under the names SNOBS, SLOBS and DOBA, acylated polyhydric alcohols, especially triacetin, ethylene glycol diacetate and 2,5-diacetoxy-2,5-dihydrofuran, and also acetylated sorbitol and mannitol and acylated sugar derivatives, especially pentaacetylglucose (PAG), sucrose polyacetate (SUPA), pentaacetylfructose, tetraacetylxylose and octaacetyllactose as well as acetylated, optionally N-alkylated glucamine and gluconolactone. It is also possible to use the combinations of conventional bleach activators known from German Patent Application DE-A-44 43 177. Nitrile compounds that form perimine acids with peroxides also come into consideration as bleach activators.
Further preferred additives to the agents according to the invention are dye fixing agents and/or polymers which, during the washing of textiles, prevent staining caused by dyes in the washing liquor that have been released from the textiles under the washing conditions.
Such polymers are preferably polyvinylpyrrolidones, polyvinylimidazole or polyvinylpyridine-N-oxides which may have been modified by the incorporation of anionic or cationic substituents, especially those having a molecular weight in the range of from 5000 to 60000, more especially from 5000 to 50000. Such polymers are usually used in an amount of from 0.01 to 5 wt-%, preferably 0.05 to 5 wt-%, especially 0.1 to 2 wt-%, based on the total weight of the detergent. Preferred polymers are those given in WO-A-02/02865 (see especially page 1, last paragraph and page 2, first paragraph).
A preferred washing agent formulation according to the invention consists of
A more preferred washing agent formulation according to the invention consists of
An especially preferred washing agent formulation according to the invention consists of
The granulates E) are prepared according to known methods. Any known method is suitable to produce granules comprising the inventive mixture. Continuous or discontinuous methods are suitable, Continuous methods, such as spray drying or fluidised bed granulation processes are preferred.
Especially suitable are spray-drying processes in which the active ingredient solution is sprayed into a chamber with circulating hot air. The atomisation of the solution is carried out using single or binary nozzles or is brought about by the spinning effect of a rapidly rotating disc. In order to increase the particle size, the spray-drying process may be combined with additional agglomeration of the liquid particles with solid nuclei in a fluidised bed that forms an integral part of the chamber (so-called fluidised spray). The fine particles (<100 μm) obtained by a conventional spray-drying process may, if necessary after being separated from the exhaust gas flow, be fed as nuclei, without being further treated, directly into the spray cone of the atomiser of the spray-dryer, for the purpose of agglomeration with the liquid droplets of the active ingredient. During the granulation step, the water can be rapidly removed from the solutions comprising phthalocyanine compound, and, where appropriate, further additives, and it is expressly intended that agglomeration of the droplets forming in the spray cone, i.e. the agglomeration of droplets with solid particles, will take place. Preference is given to the use of agglomeration processes to produce the granulates according to the invention because such processes usually yield a higher bulk weight so that the granulates have better compatibility with washing agent formulations.
A further embodiment of the present invention comprises using, for preparation of the granulates, phthalocyanine solutions that have been purified by membrane separation procedures.
If necessary, the granules formed in the spray-dryer are removed in a continuous process, for example by a sieving operation. The fines and the oversize particles are either recycled directly to the process (without being redissolved) or are dissolved in the liquid active ingredient formulation and subsequently granulated again.
The granulates are resistant to abrasion, low in dust, free-flowing and can be readily metered. They are distinguished especially by very rapid solubility in water.
The granulates E) preferably have a density in the range from 500 to 900 g/l, dissolve rapidly in water and do not float on the surface of the washing agent solution. They may be added in the desired concentration of the phthalocyanine compound directly to the washing agent formulation.
The content of granulates E) in accordance with the invention in the formulations according to the invention is from to 0.001 to 1 wt-%, preferably from 0.001 to 0.05 wt-% and very especially from 0.005 to 0.03 wt-%.
The washing agent formulation according to the invention can be prepared in a generally known manner.
A formulation in powder form can be prepared, for example, by first preparing an initial powder by spray-drying an aqueous slurry comprising all of the afore-mentioned components except for components D) and E) and then adding the dry components D) and E) and mixing all of them together. It is also possible to start from an aqueous slurry which, although comprising components A) and C), does not comprise component B) or comprises only a portion of component B). The slurry is spray-dried; component E) is then mixed with component B) and added; and then component D) is mixed in dry. The components are preferably mixed with one another in such amounts that a solid compact washing agent composition in granule form is obtained, having a specific weight of at least 500 g/l.
In another preferred embodiment, the production of the washing agent composition is carried out in three steps. In the first step a mixture of anionic surfactant (and, where appropriate, a small amount of non-ionic surfactant) and builder substance is prepared. In the second step that mixture is sprayed with the major portion of the non-ionic surfactant and then, in the third step, peroxide and, where appropriate, catalyst, and the granulate according to the invention are added. That method is usually carried out in a fluidised bed. In a further preferred embodiment, the individual steps are not carried out completely separately, so that there is a certain amount of overlap between them. Such a method is usually carried out in an extruder, in order to obtain granulates in the form of “megapearls”.
As an alternative thereto, the granulates according to the invention can, for the purpose of admixture with a washing agent in a post-dosing step, be mixed with other washing agent components such as phosphates, zeolites, brighteners or enzymes.
A mixture of that kind for post-dosing of the granulates is distinguished by a homogeneous distribution of the granulates according to the invention in the mixture and can consist of, for example, from 5 to 50% granulates and from 95 to 50% sodium tripolyphosphate. Where the dark appearance of the granulate in the washing agent composition is to be suppressed, this can be achieved, for example, by embedding the granules in droplets of a whitish meltable substance (“water-soluble wax”) or, preferably, by encapsulating the granules in a melt consisting of, for example, a water-soluble wax, as described in EP-B-0 323 407 B1, a white solid (e.g. titanium dioxide) being added to the melt in order to reinforce the masking effect of the capsule.
The detergent may also be formulated as an aqueous liquid comprising 5-50, preferably 10-35 wt-% of water or as a non-aqueous liquid detergent, containing not more than 5, preferably 0-1 wt-% of water. Non-aqueous liquid detergent compositions can contain other solvents as carriers. Low molecular weight primary or secondary alcohols exemplified by methanol, ethanol, propanol, and isopropanol are suitable. Monohydric alcohols are preferred for solubilizing surfactant, but polyols such as those containing from 2 to about 6 carbon atoms and from 2 to about 6 hydroxy groups (e.g., 1,3-propanediol, ethylene glycol, glycerine, and 1,2-propanediol) can also be used. The compositions may contain from 5 wt-% to 90 wt-%, typically 10 wt-% to 50 wt-% of such carriers. The detergents can also be present as the so-called “unit liquid dose” form.
A further embodiment of the present invention is a fabric softener formulation comprising
A preferred embodiment of the present invention is a fabric softener formulation comprising
An especially preferred embodiment of the present invention is a fabric softener formulation comprising
The preferences for the photocatalyst and the azo dyestuff as defined above also applies for the use in a fabric softener.
Fabric softeners, especially hydrocarbon fabric softeners, suitable for use herein are selected from the following classes of compounds:
Examples of cationic quatemary ammonium salts include but are not limited to:
(1) Acyclic quatemary ammonium salts having at least two C8 to C30, preferably C12 to C22 alkyl or alkenyl chains, such as: ditallowdimethyl ammonium methylsulfate, di(hydrogenated tallow)dimethyl ammonium methylsulfate, di(hydrogenated tallow)dimethyl ammonium methylchloride, distearyldimethyl ammonium methyl-sulfate, dicocodimethyl ammonium methylsulfate and the like. It is especially preferred if the fabric softening compound is a water insoluble quatemary ammonium material which comprises a compound having two C12 to C18 alkyl or alkenyl groups connected to the molecule via at least one ester link. It is more preferred if the quaternary ammonium material has two ester links present. An especially preferred ester-linked quaternary ammonium material for use in the invention can be represented by the formula:
wherein each R28 group is independently selected from C1 to C4 alkyl, hydroxyalkyl or C2 to C4 alkenyl groups; T is either —O—C(O)— or —C(O)—O—, and wherein each R29 group is independently selected from C8 to C28 alkyl or alkenyl groups; and e is an integer from 0 to 5.
A second preferred type of quatemary ammonium material can be represented by the formula:
wherein R14, e and R15 are as defined above.
(2) Cyclic quaternary ammonium salts of the imidazolinium type such as di(hydrogenated tallow)dimethyl imidazolinium methylsulfate, 1-ethylene-bis(2-tallow-1-methyl) imidazolinium methylsulfate and the like;
(3) Diamido quatemary ammonium salts such as: methyl-bis(hydrogenated tallow amidoethyl)-2-hydroxethyl ammonium methyl sulfate, methyl bi(tallowamidoethyl)2-hydroxypropyl ammonium methylsulfate and the like;
(4) Biodegradable quaternary ammonium salts such as N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium methyl sulfate and N,N-di(tallowoyl-oxy-propyl)-N,N-dimethyl ammonium methyl sulfate. Biodegradable quaternary ammonium salts are described, for example, in U.S. Pat. Nos. 4,137,180, 4,767,547 and 4,789,491 incorporated by reference herein.
Preferred biodegradable quaternary ammonium salts include the biodegradable cationic diester compounds as described in U.S. Pat. No. 4,137,180, herein incorporated by reference.
(ii) Tertiary fatty amines having at least one and preferably two C8 to C30, preferably C12 to C22 alkyl chains. Examples include hardened tallow-di-methylamine and cyclic amines such as 1-(hydrogenated tallow)amidoethyl-2-(hydrogenated tallow) imidazoline. Cyclic amines, which may be employed for the compositions herein, are described in U.S. Pat. No. 4,806,255 incorporated by reference herein.
(iii) Carboxylic acids having 8 to 30 carbons atoms and one carboxylic group per molecule. The alkyl portion has 8 to 30, preferably 12 to 22 carbon atoms. The alkyl portion may be linear or branched, saturated or unsaturated, with linear saturated alkyl preferred. Stearic acid is a preferred fatty acid for use in the composition herein. Examples of these carboxylic acids are commercial grades of stearic acid and palmitic acid, and mixtures thereof, which may contain small amounts of other acids.
(iv) Esters of polyhydric alcohols such as sorbitan esters or glycerol stearate. Sorbitan esters are the condensation products of sorbitol or iso-sorbitol with fatty acids such as stearic acid. Preferred sorbitan esters are monoalkyl. A common example of sorbitan ester is SPAN® 60 (ICI) which is a mixture of sorbitan and isosorbide stearates.
(v) Fatty alcohols, ethoxylated fatty alcohols, alkylphenols, ethoxylated alkylphenols, ethoxylated fatty amines, ethoxylated monoglycerides and ethoxylated diglycerides.
(vi) Mineral oils, and polyols such as polyethylene glycol.
These softeners are more definitively described in U.S. Pat. No. 4,134,838 the disclosure of which is incorporated by reference herein. Preferred fabric softeners for use herein are acyclic quatemary ammonium salts. Mixtures of the above mentioned fabric softeners may also be used.
The fabric softener formulation according to this invention comprises about 0.001-5 wt-%, preferably 0.001-3 wt-%, of at least one composition, which comprises at least one phthalocyanine compound of formula (1a), (1b), (2a), (3), (4), (4a), (5), (6) and/or (7), and at least one azo dyestuff of formulae
wherein
A preferred fabric softener formulation according to this invention comprises about 0.001-5 wt-%, preferably 0.001-3 wt-%, of at least one composition, which comprises at least one phthalocyanine compound of formula (1 a), (1b), (2a), (3), (4), (4a), (5), (6) and/or (7), and
at least one azo dyestuff of formula (A), (B), and/or (C) and/or
at least one triphenylmethane dyestuff of formula (D), (E), (F), (G), (H) and/or (I) as defined above, based on the total weight of the fabric softener formulation.
The fabric softener formulation employed in the present invention preferably contains about 0.1 to about 95 wt-%, based on the total weight of the fabric softening composition, of the fabric softener formulation. Preferred is an amount of 0.5 to 50 wt-%, especially an amount of 2 to 50 wt-% and most preferably an amount of 2 to 30 wt-%.
The fabric softening composition may also comprise additves which are customary for standard commercial fabric softening compositions, for example alcohols, such as ethanol, n-propanol, i-propanol, polyhydric alcohols, for example glycerol and propylene glycol; amphoteric and nonionic surfactants, for example carboxyl derivatives of imidazole, oxyethylated fatty alcohols, hydrogenated and ethoxylated castor oil, alkyl polyglycosides, for example decyl polyglucose and dodecylpolyglucose, fatty alcohols, fatty acid esters, fatty acids, ethoxylated fatty acid glycerides or fatty acid partial glycerides; also inorganic or organic salts, for example water-soluble potassium, sodium or magnesium salts, non-aqueous solvents, pH buffers, perfumes, dyes, hydrotropic agents, antifoams, anti redeposition agents, enzymes, optical brighteners, antishrink agents, stain removers, germicides, fungicides, dye fixing agents or dye transfer inhibitors (as described in WO-A-02/02865), antioxidants, corrosion inhibitors, wrinkle recovery or wet soiling reduction agent, such as polyorganosiloxanes. The latter two additives are described in WO0125385.
Such additives are preferably used in an amount of 0 to 30 wt-%, based on the total weight of the fabric softening composition. Preferred is an amount of 0 to 20 wt-%, especially an amount of 0 to 10 wt-% and most preferably an amount of 0 to 5 wt-%, based on the total weight of the fabric softening composition.
The fabric softener compositions are preferably in liquid aqueous form. The fabric softener compositions preferably contain a water content of 25 to 90 wt-%, based on the total weight of the composition. More preferably the water content is 50 to 90 wt-%, especially 60 to 90 wt-%.
A preferred embodiment of the present invention is a fabric softener formulation comprising
A more preferred embodiment of the present invention is a fabric softener formulation comprising
The fabric softener compositions preferably have a pH value from 2.0 to 9.0, especially 2.0 to 5.0.
The fabric softener compositions can, for example, be prepared as follows:
Firstly, an aqueous formulation of the cationic polymer is prepared as described above. The fabric softener composition according to the invention is usually, but not exclusively, prepared by firstly stirring the active substance, i.e. the hydrocarbon based fabric softening component, in the molten state into water, then, where required, adding further desired additives and, finally, adding the formulation of the cationic polymer. The fabric softener composition can, for example, also be prepared by mixing a preformulated fabric softener with the cationic polymer.
These fabric softener compositions are traditionally prepared as dispersions containing for example up to 30 wt-% of active material in water. They usually have a turbid appearance. However, alternative formulations usually containing actives at levels of 5 to 40 wt-% along with solvents can be prepared as microemulsions, which have a clear appearance (as to the solvents and the formulations see for example U.S. Pat. No. 5,543,067 und WO-A-98/17757).
Examples of suitable textile fibre materials which can be treated with the liquid rinse conditioner composition are materials made of silk, wool, polyamide, acrylics or polyurethanes, and, in particular, cellulosic fibre materials and blends of all types. Such fibre materials are, for example, natural cellulose fibres, such as cotton, linen, jute and hemp, and regenerated cellulose. Preference is given to textile fibre materials made of cotton. The fabric softener compositions are also suitable for hydroxyl-containing fibres which are present in mixed fabrics, for example mixtures of cotton with polyester fibres or polyamide fibres. The following Examples serve to illustrate the invention without the invention being limited thereto. Parts and percentages are by weight unless specified otherwise. Temperature is given in degree Celsius unless specified otherwise.
Degradation Experiments
The aqueous mixture of the photocatalyst and the dyestuff or the components alone were exposed in the given concenctration in a closed 250 ml glass bottle, containing 125 ml of the mixture to sunlight. The intensity measured with a Roline RO-1322 Digital Lux meter in front of the bottles was within the range of 4500-6000 Lux.
The degradation of the components was determined from spectrophotometric data gained HP 8452 Diode array spectrophotometer. The absorption of the mixtures was measured at the respective absorption maximum of the components. (Photocatalyst 670 nm, Dyestuff 550 nm). While there is only a small overlap of the two absorption spectrum at the maximum absorption of the photocatalyst at 670 nm, there may be an appreciable overlap at the absorption maximum of the dyestuff. The absorption was determined at the start and then every 2 hours. The loss after two hours is given in percentage of the initial concentration and is corrected where the overlap is considerable.
The used photocatalysts are
The results are summarized in Table 1.
Determination of Hue Angle
The hue angle was determined from the experimental spectra of the starting mixture collected in the transmission mode, using the ordinary calculation modulus for the chosen light source (D 65 or A) and 10° observer. The mixtures are prepared in analogy to the Degradation Examples 1-17.
The results are summarized in Table 2
| Number | Date | Country | Kind |
|---|---|---|---|
| 03102447.4 | Aug 2003 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP04/51627 | 7/28/2004 | WO | 2/3/2006 |
