Fabric softener composition

Description

The present invention relates to a fabric softener composition and to a process for the bleaching of textile fibre materials using this fabric softener composition.

In customary household washing processes for whites, such as bed linen, table linen and white cotton fabrics, the laundry items to be treated are normally subjected to a combined washing and bleaching process in which the items of laundry are treated in an aqueous bath comprising, as active substance, an organic detergent and a bleach. Processes for bleaching or removing stains from textiles using water-soluble phthalocyanine compounds are known, for example, from U.S. Pat. Nos. 3,927,967, 4,094,806 and 4,033,718.

The object of the present invention is to use water-soluble phthalocyanine compounds as photobleaching agents in certain fabric softener compositions comprising, as active substance, ester quats, which are quaternary ammonium compounds having at least one long-chain hydrophobic alkyl or alkenyl group interrupted by carboxyl groups. Fabric softeners containing ester quats are described, for example, in EP-A-0 239 910 or WO 95/24460.

Surprisingly, it has now been found that fabric softener compositions comprising water-soluble phthalocyanine compounds of a cationic, neutral or anionic nature bring about particularly good bleaching effects if textiles are treated in an aqueous fabric softener bath comprising these compositions, the textiles being irradiated with light in the visible and/or infrared region or in the daylight in the fabric softener bath itself or subsequently in the damp state.

The present invention thus relates to a fabric softener composition comprising

(a) 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); and

(b) a quaternary ammonium compound of the formula

in which

R

1

and R

2

independently of one another are C

1

-C

5

alkyl; or hydroxy-C

1

-C

5

alkyl;

A is the radical of the formula

or the radical of the formula

B is C

1

-C

5

alkyl; a C

8

-C

20

fatty acid radical; the radical of the formula (1a) or the, radical of the formula (1b);

R

3,

R

4

and R

5

independently of one another are a C

8

-C

20

fatty acid radical;

X

1

−

is a softener-compatible anion; and

m, n and p are numbers from 0 to 5.

The novel composition advantageously comprises, as photobleaching agent, a compound of the formula

in which

PC is the phthalocyanine ring system;

Me is Zn, Fe(II), Ca, Mg, Na, K, Al—Z

1

, Si(IV), P(V), Ti(IV), Ge(IV), Cr(VI), Ga(III), Zr(IV), In(III), Sn(IV) or Hf(VI);

Z

1

is a halide, sulfate, nitrate, carboxylate, alkanolate, or hydroxyl ion;

q is 0, 1 or 2;

r is 1 to 4;

Q

1

is a sulfo or carboxyl group; or a radical of the formula

—SO

2

X

2

—R

6

—X

3

+

, —O—R

6

—X

3

+

; or —(CH

2

)

t

—Y

1

+

;

in which

R

6

is a branched or unbranched C

1

-C

8

alkylene; or 1,3- or 1,4-phenylene;

X

2

is —NH—; or —N—C

1

-C

5

alkyl;

X

3

+

is a group of the formula

or, in the case where R

6

=C

1

-C

8

alkylene, also a group of the formula

Y

1

+

is a group of the formula

t is 0 or 1;

where in the above formulae

R

7

and R

8

independently of one another are C

1

-C

6

alkyl;

R

9

is C

1

-C

6

alkyl; C

5

-C

7

cycloalkyl; or NR

11

R

12

;

R

10

and R

11

independently of one another are C

1

-C

5

alkyl;

R

12

and R

13

independently of one another are hydrogen or C

1

-C

5

alkyl;

R

14

and R

15

independently of one another are unsubstituted C

1

-C

6

alkyl or C

1

-C

6

alkyl substituted by hydroxyl, cyano, carboxyl, carb-C

1

-C

6

alkoxy, C

1

-C

6

alkoxy, phenyl, naphthyl or pyridyl;

u is from 1 to 6;

A

1

is a unit which completes an aromatic 5- to 7-membered nitrogen heterocycle, which may where appropriate also contain one or two further nitrogen atoms as ring members, and

B

1

is a unit which completes a saturated 5- to 7-membered nitrogen heterocycle, which may where appropriate also contain 1 to 2 nitrogen, oxygen and/or sulfur atoms as ring members;

Q

2

is hydroxyl; C

1

-C

22

alkyl; branched C

4

-C

22

alkyl; C

2

-C

22

alkenyl; branched C

4

-C

22

alkenyl and mixtures thereof; C

1

-C

22

alkoxy; a sulfo or carboxyl radical; a radical of the formula

a branched alkoxy radical of the formula

an alkylethyleneoxy unit of the formula —(T

1

)

d

—(CH

2

)

b

(OCH

2

CH

2

)

a

—B

3

or an ester of the formula COOR

23

in which

B

2

is hydrogen; hydroxyl; C

1

-C

30

alkyl; C

1

-C

30

alkoxy; —CO

2

H; —CH

2

COOH; SO

3

−

M

1

+

; —OSO

3

−

M

1

+

; —PO

3

2−

M

1

; —OPO

3

2−

M

1

; and mixtures thereof;

B

3

is hydrogen; hydroxyl; —COOH; —SO

3

−

M

1

+

; —OSO

3

−

M

1

+

; C

1

-C

6

alkoxy;

M

1

is a water-soluble cation;

T

1

is —O—; or —NH—;

X

1

and X

4

independently of one another are —O—; —NH—; or —N—C

1

-C

5

alkyl;

R

16

and R

17

independently of one another are hydrogen, a sulfo group and salts thereof, a carboxyl group and salts thereof or a hydroxyl group, at least one of the radicals R

16

and R

17

being a sulfo or carboxyl group or salts thereof,

Y

2

is —O—, —S—, —NH—or —N—C

1

-C

5

alkyl;

R

18

and R

19

independently of one another are hydrogen, C

1

-C

6

alkyl, hydroxy-C

1

-C

6

alkyl, cyano-C

1

-C

6

alkyl, sulfo-C

1

-C

6

alkyl, carboxy or halogen-C

1

-C

6

alkyl; unsubstituted phenyl or phenyl substituted by halogen, C

1

-C

4

alkyl or C

1

-C

4

alkoxy, sulfo or carboxyl or R

18

and R

19

together with the nitrogen atom to which they are bonded are a saturated 5- or 6-membered heterocyclic ring which may additionally also contain a nitrogen or oxygen atom as a ring member;

R

20

and R

21

independently of one another are C

1

-C

6

alkyl or aryl-C

1

-C

6

alkyl radicals;

R

22

is hydrogen; an unsubstituted C

1

-C

6

alkyl or C

1

-C

6

alkyl substituted by halogen, hydroxyl, cyano, phenyl, carboxyl, carb-C

1

-C

6

alkoxy or C

1

-C

6

alkoxy;

R

23

is C

1

-C

22

alkyl, branched C

4

-C

22

alkyl, C

1

-C

22

alkenyl or branched C

4

-C

22

alkenyl; C

3

-C

22

glycol; C

1

-C

22

alkoxy; branched C

4

-C

22

alkoxy; and mixtures thereof;

M is hydrogen; or an alkali metal ion or ammonium ion,

Z

2

is a chlorine, bromine, alkylsulfate or aralkylsulfate ion;

a is 0 or 1;

b is from 0 to 6;

c is from 0 to 100;

d is 0; or 1;

e is from 0 to 22;

v is an integer from 2 to 12;

w is 0 or 1; and

A is an organic or inorganic anion, and

s is equal to r in cases of monovalent anions A

−

and is ≦r in cases of polyvalent anions, it being necessary for A

s

−

to compensate the positive charge; where, when r≠1, the radicals Q

1

can be identical or different,

and where the phthalocyanine ring system may also comprise further solublising groups.

The number of substituents Q

1

and Q

2

in the formula (2a) and (2b) 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 C

1

-C

6

alkyl, C

1

-C

6

alkoxy, halogen, carboxyl, carb-C

1

-C

6

alkoxy, hydroxyl, amino, cyano, sulfo, sulfonamido, etc.

Preference is given to a substituent from the group C

1

-C

6

alkyl, C

1

-C

6

alkoxy, halogen, carboxyl, carb-C

1

-C

6

alkoxy or hydroxyl.

Particularly suitable groups

are:

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 (2a) 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; A

s

−

can thus also be a sulfate, sulfite, carbonate, phosphate, nitrate, acetate, oxalate, citrate, lactate ion or another anion of an organic carboxylic add. 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.

C

1

-C

6

alkyl and C

1

-C

6

alkoxy 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.

C

2

-C

22

alkenyl 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.

The C

8

-C

20

fatty acid radicals defined for the quaternary ammonium compounds of the formula (1) are derived from saturated or unsaturated fatty acids, such as, for example, from capric, lauric, myristic, palmitic, stearic, dodecyl; pentadecyl; hexadecyl or oleyl acid; or decanoic, dodecanoic, tetradecanoic, hexadecanoic, oleic, linoleic, linolenic, ricinoleic acid, coconut fatty acid, or preferably tallow fatty acid.

Preferred photobleaching agents of the formula (2a) of the novel composition have the formula

in which

PC, X

2

, X

3

, and R

6

are as defined above;

M is hydrogen, an alkali metal ion, ammonium ion or amine salt ion; and the sum of the numbers r

1

and r

2

is from 1 to 4 and

A

s

balances exactly the positive charge on the remainder of the molecule, and in particular the formula

in which

PC is as defined in formula (2a),

R

6

′ is C

2

-C

6

alkylene;

r

1

is a number from 1 to 4;

X

3

′ is a group of the formula

in which

R

7

and R

8

independently of one another are unsubstituted C

1

-C

4

alkyl or C

1

-C

4

alkyl substituted by hydroxyl, cyano, halogen or phenyl;

R

9

is R

7

; cyclohexyl or amino;

R

11

is C

1

-C

4

alkyl;

R

21

is C

1

-C

4

alkyl; C

1

-C

4

alkoxy; halogen, carboxyl, carb-C

1

-C

4

alkoxy or hydroxyl; and

A″ is a halide, alkylsulfate or arylsulfate ion;

it being possible for the radicals —SO

2

NHR′

6

—X

3

′

+

A

−

to be identical or different.

Other photobleaching agents which can be used according to the invention have the formula

in which

PC is the phthalocyanine ring system;

Me is Zn, Fe(II), Ca, Mg, Na, K, Al—Z

1

, Si(IV), P(V), Ti(IV), Ge(IV), Cr(VI), Ga(III), Zr(IV), In(III), Sn(IV) or Hf(VI);

Z

1

is a halide, sulfate, nitrate, carboxylate, alkanolate, or hydroxyl ion;

q is 0; 1; or 2;

Y

3

′ is hydrogen, an alkali metal ion or ammonium ion; and

r is any number from 1 to 4.

Very particularly preferred phthalocyanine compounds have the formula (5), in which

Me is Zn or Al—Z

1

; and

Z

1

is a halide, sulfate, nitrate, carboxylate, alkanolate, or hydroxyl ion.

Other interesting phthalocyanine compounds which can be used according to the invention have the formula

in which

PC, Me and q are as defined in formula (5);

R

17

′ and R

18

′ independently of one another are hydrogen, phenyl, sulfophenyl, carboxyphenyl, C

1

-C

6

alkyl, hydroxy-C

1

-C

6

alkyl, cyano-C

1

-C

6

alkyl, sulfo-C

1

-C

6

alkyl, carboxy-C

1

-C

6

alkyl or halogen-C

1

-C

6

alkyl or together with the nitrogen atom form the morpholine ring;

q′ is an integer from 2 to 6; and

r is a number from 1 to 4;

where, if r is >1, the radicals

present in the molecule may be identical or different.

Further interesting phthalocyanine compounds which can be used according to the invention have the formula

in which

PC, Me and q are as defined in formula (5),

Y′

3

is hydrogen, an alkali metal ion or ammonium ion,

q′ is an integer from 2 to 6;

R

17

′ and R

18

′ independently of one another are hydrogen, phenyl, sulfophenyl, carboxyphenyl, C

1

-C

6

alkyl, hydroxy-C

1

-C

6

alkyl, cyano-C

1

-C

6

alkyl, sulfo-C

1

-C

6

alkyl, carboxy-C

1

-C

6

alkyl or halogen-C

1

-C

6

alkyl or together with the nitrogen atom form the morpholine ring;

m′ is 0 or 1; and

r and r

1

independently of one another are any number from 0.5 to 3, the sum r+r

1

being

at least 1, but no more than 4.

If the central atom Me in the phthalocyanine ring is Si(IV), the phthalocyanines used according to the invention may also have axial substituents (=R

24

) in addition to the substituents on the phenyl ring of the phthalocyanine ring. Such phthalocyanines have, for example, the formula

in which

R

24

is hydroxyl; C

1

-C

22

alkyl; branched C

4

-C

22

alkyl; C

1

-C

22

alkenyl; branched C

4

-C

22

alkenyl and mixtures thereof; C

1

-C

22

alkoxy; a sulfo or carboxyl radical; a radical of the formula

a branched alkoxy radical of the formula

an alkylethyleneoxy unit of the formula —(T

1

)

d

—(CH

2

)

b

(OCH

2

CH

2

)

a

—B

3

or an ester of the formula COOR

23

; and

U is [Q

1

]

r

+

A

s

−

; or Q

2

.

R

16

, R

17

, R

18

, R

19

, R

20

, R

21

, R

22

, R

23

, B

2

, B

3

, M, M

1

, Q

1

, Q

2

, A

s

, T

1

, X

1

, Y

2

, Z

2

, a, b, c, d, e, r, v, w are as defined in the formulae (2a) and (2b).

Quaternary ammonium compounds of the component (b) preferably used according to the invention are compounds of the formula (1) in which

X

1

is a halogen atom; —CH

3

SO

4

−

; —C

2

H

5

SO

4

−

; or —NO

3

−

.

Quaternary ammonium compounds which are particularly preferably used according to the invention are those of the formula (1) in which

A and B independently of one another are the radical of the formula (1a) or (1b), or those compounds of the formula (1) in which A and B are the radical of the formula (1b).

Very particularly preferred quaternary ammonium compounds have the formula

in which

R

1

, R

2

and B are C

1

-C

5

alkyl;

R

3

is the aliphatic radical of tallow fatty acid; and

X

3

−

is a halogen atom.

Further interesting quaternary ammonium compounds have the formula

in which

R

1

and R

2

are C

1

-C

5

alkyl;

R

3

is the aliphatic radical of tallow fatty acid and

X

3

−

is a halogen atom.

Preference is given to using fabric softener compositions comprising

(a) a water-soluble phthalocyanine of the formula (5); and

(b) a quaternary ammonium compound of the formula (8).

Preference is also given to using fabric softener compositions comprising

(a) a water-soluble phthalocyanine of the formula (10) and

(b) a quaternary ammonium compound of the formula (8).

The photobleaching agents used according to the invention are used in the fabric softener composition only in small amounts and thus have a catalytic effect.

The novel fabric softener compositions preferably comprise from 0.0001 to 0.05% by weight, preferably from 0.001 to 0.005% by weight, of component (a) and from 1 to 20% by weight, preferably from 5 to 20% by weight, of component (b).

The novel fabric softener composition may also comprise additives customary for standard commercial fabric softeners, such as alcohols, such as, for example, ethanol, n-propanol, i-propanol, polyhydric alcohols, such as, for example, glycerol and propylene glycol; amphoteric and nonionic surfactants, such as, for example, carboxyl derivatives of imidazole, oxethylated fatty alcohols, hydrogenated and ethoxylated castor oil, alkyl polyglycosides, for example decylpolyglucose and dodecylpolyglucose, fatty alcohols, fatty acid esters, fatty acids, ethoxylated fatty acid glycerides or fatty acid partial glycerides; also relatively small amounts of dyes, perfumes, buffer substances, inorganic or organic salts, such as, for example, water-soluble potassium, sodium or magnesium salts, non-aqueous solvents, pH buffers, hydrotropic agents, antifoams, corrosion inhibitors, antiredeposition agents, viscosity regulators, in particular polymeric or other thickeners, stabilisers, enzymes, optical brighteners, antishrink agents, stain removers, antimicrobial agents, germicides, fungicides, antioxidants, and anticrease agents.

The novel fabric softener composition is usually liquid. The active ingredients present therein are preferably emulsified in water. Preparation usually involves firstly stirring the active substance, i.e. the quaternary ammonium compound of the formula (1) in the molten state into water, then, where required, adding further desired additives and, finally, after cooling, adding the phthalocyanine compound as a diluted stock solution.

Another subject-matter of the invention is a process for the bleaching of textiles using a photobleaching agent, which comprises treating soiled textiles in a bath of a fabric softener composition comprising

(a) 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), Sn(III), Sn(IV) or Hf(VI) phthalocyanine; and

(b) a quaternary ammonium compound of the formula (1),

with irradiation with visible and/or infrared light or daylight, either on the fabric softener bath directly or on the damp textiles outside the fabric softener bath, and in the presence of oxygen.

The novel composition is used in the manner customary for known fabric softeners, the photobleaching agent only becoming effective upon irradiation with light, as described, for example, in U.S. Pat. No. 4,166,718. For example, textiles washed in a customary washing cycle are post-treated in a liquor comprising a novel fabric softener composition in a rinsing operation. Irradiation with visible and/or infrared light can be carried out directly in the fabric softener liquor, for example using a suitable artificial light source in the washing machine. Irradiation can, however, also be preferably carried out after the textiles have been removed from the rinsing bath in the damp state, the light source used preferably being sunlight. In this case, exposure can suitably be carried out while the textiles are drying. If the textiles are not dried on a line, but, for example, in a tumbledryer, exposure may also take place during this drying process, for example using a suitable artificial light source, fixed to or in the tumbledryer. For the photobleaching agent to be effective, the presence of oxygen is also required. The oxygen present (dissolved) in the wash liquor (the liquor should as far as possible contain no reducing agent) or the (dissolved) oxygen which is present in the liquor or atmospheric oxygen when exposure takes place outside the bath is sufficient.

Examples of suitable textile fibre materials which may be treated with the novel fabric softener composition are materials made of silk, wool, polyamide or polyurethanes, and in particular cellulosic fibre materials of all types. Examples of such fibre materials are the natural cellulose fibres, such as cotton, linen, jute and hemp, and also pulp and regenerated cellulose. Preference is given to textile fibre materials made of cotton. The novel fabric softener compositions are also suitable for hydroxyl group-containing fibres which are present in mixed fibres, for example mixtures of cotton with polyester fibres or polyamide fibres.

The effect of the photobleaching agent considerably improves removal of stains from the treated fabric. In addition, colour transfer between individual fabric articles can be prevented or reduced.

Furthermore, the novel composition has the advantage that the effect of the essential components is not mutually influenced, so that the bleaching effect of the photobleaching agent is not impaired by the quaternary ammonium compound and vice versa.

The examples below serve to illustrate the invention without limiting it thereto.

EXAMPLES 1 TO 4

Preparation of the Fabric Softener Formulations

TABLE 1

Compound of

Concentration

Amount of

the formula

of the

Amount of the

amount of

compound of

(102) based on

formulation

formulation

water used

the formula

fabric softener

Example

(102) [%]

(102) used [g]

[g]

(102) [mg]

formulation [%]

1

0

0.0

0.9

0.0

0.0

2

0.0038

0.9

0.0

0.345

0.00115

3

0.23

0.45

0.45

1.035

0.00345

4

0.23

0.9

0.0

2.074

0.00690

29.1 g of a fabric softener comprising, as active substance 4.5 g (15% with respect to the fabric softener formulation), of the compound of the formula

are introduced initially into a 50 ml bottle. 0.9 g of water or a mixture of water and the given amount of the formulation comprising as active substance a compound of the formula

AlClPC(SO

3

H)

3-4

(102)

are added thereto. The bottle is then screwed tightly shut and vigorously shaken several times.

A viscous homogeneous liquid is formed.

EXAMPLE 5

a) A 250 g cotton fabric soiled with red wine and 750 g of bleached cotton fabric used as ballast are washed at 30° C. in 10 l of water using a commercially available detergent in a washing machine for 15 minutes.

After the washing operation, the washed cotton fabric is rinsed under running water.

b) A second rinsing operation is carried out using the formulations from Examples 1 to 4. For this purpose, the two laundry articles washed and rinsed under a) are washed with 6 l of water and 30 g of each of the formulations from Examples 1 to 4 for 5 minutes at 30° C. in a washing machine. The items of laundry are then spun dry.

1 part of the items of laundry treated in this way is subsequently ironed dry, and the other part is exposed in the damp state under Osram lamps for 2 hours and subsequently ironed dry.

The degree of bleaching of the test fabric is then measured using a photometer in the form of brightness values (=Y), expressed in %, based on the absolute whiteness in accordance with the CIE recommendation of 1.1.1969. The results obtained are summarised in Table 2.

TABLE 2

Formulation from

without exposure

with exposure for 2 hours

Example

Y [%]

ΔY

Y [%]

ΔY

1

68.1

71.1

2

67.9

−0.2

74

2.9

3

67.3

−0.8

75.9

4.8

4

67.6

−0.5

77.8

6.7

The results show that significantly higher brightness values are achieved using the novel fabric softener composition after exposure for two hours.

EXAMPLE 6

The procedure is as described in Example 5, with the difference that cotton with tea is used.

The results are given in Table 3:

TABLE 3

Formulation from

without exposure

with exposure for 2 hours

Example

Y [%]

ΔY

Y [%]

ΔY

1

58.1

59.1

2

58.2

0.1

60.5

1.4

3

58

−0.1

61.2

2.1

4

57.9

−0.2

63.3

4.2

The results show that significantly higher brightness values are achieved using the novel fabric softener composition after exposure for two hours.

EXAMPLE 7

The procedure is as described in Example 5, with the difference that cotton fabric soiled with coffee is used.

The results are given in Table 4:

TABLE 4

without

with exposure for

with exposure for

Formulation from

exposure

2 hours

4 hours

Example

Y [%]

ΔY

Y [%]

ΔY

Y [%]

ΔY

1

79.4

81.2

83.4

2

78.6

−0.8

84.5

3.3

87

3.6

3

78.6

−0.8

86.3

5.1

88.7

5.3

4

78.7

−0.7

86.5

5.3

89

5.6

The results show that significantly higher brightness values are achieved using the novel fabric softener composition after exposure for 2 and 4 hours.

EXAMPLE 8

Preparation of a Fabric Softener Formulation

7.5 g of the compound of the formula

are diluted with water to 40 g and stirred at 50-60° C. in a water bath to give a homogeneous paste, giving a 18.75% strength aqueous formulation of the compound of the formula (103) (=formulation 8a).

0.15 g of a 2% strength solution of the compound of the formula (102) and 1.85 g of water are added to 8.0 g of this paste, and the whole mixture is stirred at 50-60° C. in a water bath to give a homogeneous paste.

The resulting fabric softener formulation comprises

15% of the compound of the formula (103) and

0.00345% of the compound of the formula (102)

(=formulation 8b).

EXAMPLE 9

Washing Test

a. Washing with Test Detergent

1 kg of fabric, consisting of 250 g of cotton fabric soiled with red wine, coffee and tea, and

750 g of bleached cotton fabric as ballast are washed with

10 litres of water and

40 g of a 16% alkylarylsulfonate, 40% of sodium triphosphate, 4% of fatty alcohol sulfate,

4% of sodium silicate, 2% of magnesium silicate and 3% of syndet soap comprising coconut

acid ethanolamine (serves as test detergent)

for 15 minutes at 30° C. in a Linitest laboratory washing machine.

After the wash, the fabric is rinsed under running water.

b. Rinsing with the Formulation from Example 8

1000 g of the cotton fabric washed in a. are rinsed with 6 litres of water and 30 g of the rinse formulations 8a and 8b for 5 minutes at 30° C. in a washing machine and subsequently spun dry.

1 part of the fabric is ironed dry.

1 part of the fabric soiled with wine and coffee is exposed in the damp state to Osram lamps

for 4 hours and subsequently ironed dry.

The fabric soiled with tea is exposed in the damp state using Osram lamps for 2 hours and subsequently ironed dry.

Furthermore, the rinsing and exposure process in the case of the fabric soiled with tea is repeated three times and five times (1, 3 or 5 cycles). The results are given in Table 5.

TABLE 5

Results of the washing test of the fabric soiled with red wine or coffee

fabric soiled with red wine

fabric soiled with coffee

Y(Start) = 52.3

Y(Start) = 73.7

without

with exposure

without

with exposure

exposure

for 4 hours

exposure

for 4 hours

Y

ΔY

Y

ΔY

Y

ΔY

Y

ΔY

Formulation

66.1

66.2

77.9

80.2

8a)

Formulation

65.0

1.1

71.5

5.3

79.4

1.5

86.9

6.7

8b)

The results show that significantly higher brightness values are achieved with the novel fabric softener composition after exposure for 4 hours.

TABLE 6

Results of the washing test of the fabric soiled with tea

fabric soiled with tea

Y(Start) = 35.5

after 1 washing cycle

after 3 washing cycles

after 5 washing cycles

none

2 hours

none

2 hours

none

2 hours

Exposure

Y

ΔY

Y

ΔY

Y

ΔY

Y

ΔY

Y

ΔY

Y

ΔY

Formulation

40.6

40.7

41.2

44.7

41.3

49.9

8a)

Formulation

40.2

−0.4

43.4

2.7

41.6

0.4

53.4

8.7

41.6

0.3

63.5

13.6

8b)

The results show that significantly higher brightness values are achieved using the novel fabric softener composition.

Claims

1. A rinse-added fabric softener composition comprising(a) 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); and (b) a quaternary ammonium compound of the formula in which R1 and R2 independently of one another are C1-C5alkyl; or hydroxy-C1-C5alkyl; A is the radical of the formula or the radical of the formula B is C1-C5alkyl; a C8-C20 fatty acid radical; the radical of the formula (1a) or the radical of the formula (1b); R3, R4 and R5 independently of one another are a C8-C20 fatty acid radical; X1− is a softener-compatible anion; and m, n and p are numbers from 0 to 5.
2. A composition according to claim 1, which comprises a phthalocyanine of the formula in whichPC is the phthalocyanine ring system; Me is Zn, Fe(II), Ca, Mg, Na, K, Al—Z1, Si(IV), P(V), Ti(IV), Ge(IV), Cr(VI), Ga(III), Zr(IV), In(III), Sn(IV) or Hf(VI); Z1 is a halide, sulfate, nitrate, carboxylate, alkanolate, or hydroxyl ion; q is 0, 1 or 2; r is 1 to 4; Q1 is a sulfo or carboxyl group; or a radical of the formula —SO2X2—R6—X3+, —O—R6—X3+; or —(CH2)t—Y1+; in which R6 is a branched or unbranched C1-C8alkylene; or 1,3- or 1,4-phenylene;X2 is —NH—; or —N—C1-C5alkyl; X3+ is a group of the formula or, in the case where R6=C1-C8alkylene, also a group of the formula Y1+ is a group of the formula t is 0 or 1; where in the above formulae R7 and R8 independently of one another are C1-C6alkyl; R9 is C1-C6alkyl; C5-C7cycloalkyl; or NR11R12; R10 and R11 independently of one another are C1-C5alkyl; R12 and R13 independently of one another are hydrogen or C1-C5alkyl; R14 and R15 independently of one another are unsubstituted C1-C6alkyl or C1-C6alkyl substituted by hydroxyl, cyano, carboxyl, carb-C1-C6alkoxy, C1-C6alkoxy, phenyl, naphthyl or pyridyl; u is from 1 to 6; A1 is a unit which completes an aromatic 5- to 7-membered nitrogen heterocycle, which may also contain one or two further nitrogen atoms as ring members, and B1 is a unit which completes a saturated 5- to 7-membered nitrogen heterocycle, which may also contain 1 to 2 nitrogen, oxygen and/or sulfur atoms as ring members; Q2 is hydroxyl; C1-C22alkyl; branched C4-C22alkyl; C2-C22alkenyl; branched C4-C22alkenyl and mixtures thereof; C1-C22alkoxy; a sulfo or carboxyl radical; a radical of the formula a branched alkoxy radical of the formula an alkylethyleneoxy unit of the formula —(T1)d—(CH2)b(OCH2CH2)a—B3 or an ester of the formula COOR23 in which B2 is hydrogen; hydroxyl; C1-C30alkyl; C1-C30alkoxy; —CO2H; —CH2COOH; SO3−M1+; —OSO3−M1+; —PO32−; M1; —OPO32−M1; and mixtures thereof; B3 is hydrogen; hydroxyl; —COOH; —SO3−M1+; —OSO3−M1+; C1-C6alkoxy; M1 is a water-soluble cation; T1 is —O—; or —NH—; X1 and X4 independently of one another are —O—; —NH—; or —N—C1-C5alkyl; R16 and R17 independently of one another are hydrogen, a sulfo group and salts thereof, a carboxyl group and salts thereof or a hydroxyl group, at least one of the radicals R16 and R17 being a sulfo or carboxyl group or salts thereof, Y2 is —O—, —S—, —NH— or —N—C1-C5alkyl; R18 and R19 independently of one another are hydrogen, C1-C6alkyl, hydroxy-C1-C6alkyl, cyano-C1-C6alkyl, sulfo-C1-C6alkyl, carboxyl or halogen-C1-C6alkyl; unsubstituted phenyl or phenyl substituted by halogen, C1-C4alkyl or C1-C4alkoxy, sulfo or carboxyl or R18 and R19 together with the nitrogen atom to which they are bonded are a saturated 5- or 6-membered heterocyclic ring which may additionally also contain a nitrogen or oxygen atom as a ring member; R20 and R21 independently of one another are C1-C6alkyl or aryl-C1-C6alkyl radicals; R22 is hydrogen; or unsubstituted C1-C6alkyl or C1-C6alkyl substituted by halogen, hydroxyl, cyano, phenyl, carboxyl, carb-C1-C6alkoxy or C1-C6alkoxy; R23 is C1-C22alkyl, branched C4-C22alkyl, C1-C22alkenyl or branched C4-C22alkenyl; C3-C22glycol; C1-C22alkoxy; branched C4-C22alkoxy; and mixtures thereof; M is hydrogen; or an alkali metal ion or ammonium ion, Z2 is a chlorine, bromine, alkylsulfate or aralkylsulfate ion; a is 0 or 1; b is from 0 to 6; c is from 0 to 100; d is 0; or 1; e is from 0 to 22; v is an integer from 2 to 12; w is 0 or 1; and A is an organic or inorganic anion, and s is equal to r in cases of monovalent anions A− and is ≦r in cases of polyvalent anions; it being necessary for As− to compensate the positive charge; where, when r≠1, the radicals Q1 can be identical or different, and where the phthalocyanine ring system may also comprise further solublising groups.
3. A composition according to claim 1, which comprises a phthalocyanine of the formula in whichPC is the phthalocyanine ring system R6′ is C2-C6alkylene; r is a number from 1 to 4; X3′+ is a group of the formula in which R7 and R8 independently of one another are unsubstituted C1-C4alkyl or C1-C4alkyl substituted by hydroxyl, cyano, halogen or phenyl; R9 is R7; cyclohexyl or amino; R11 is C1-C4alkyl; R21 is C1-C4alkyl; C1-C4alkoxy; halogen, carboxyl, carb-C1-C4alkoxy or hydroxyl; and A′ is a halide, alkylsulfate or arylsulfate ion; it being possible for the radicals —SO2NHR′6—X3′+A− to be identical or different.
4. A composition according to claim 1, which comprises phthalocyanines of the formula in whichPC is the phthalocyanine ring system; Me is Zn, Fe(II), Ca, Mg, Na, K, Al—Z1, Si(IV), P(V), Ti(IV), Ge(IV), Cr(VI), Ga(III), Zr(IV), In(III), Sn(IV) or Hf(VI); Z1 is a halide, sulfate, nitrate, carboxylate, alkanolate, or hydroxyl ion; q is 0; 1; or 2; Y3′ is hydrogen; an alkali metal ion or ammonium ion; and r is any number from 1 to 4.
5. A composition according to claim 4, wherein in formula (5)Me is Zn or Al—Z1; and Z1 is a halide, sulfate, nitrate, carboxylate, alkanolate, or hydroxyl ion.
6. A composition according to claim 1, which comprises a phthalocyanine of the formula in whichR24 is hydroxyl; C1-C22alkyl; branched C4-C22alkyl; C1-C22alkenyl; branched C4-C22alkenyl and mixtures thereof; C1-C22alkoxy; a sulfo or carboxyl radical; a radical of the formula radical of the formula an alkylethyleneoxy unit of the formula —(T1)d—(CH2)b(OCH2CH2)a—B3 or an ester of the formula COOR23; and U is [Q1]r+As−; or Q2; and R16, R17, R18, R19, R20, R21, R22, R23, B2, B3, M, M1, Q1, Q2, As, T1, X1, Y2, Z2, a, b, c, d, e, r, v, w are as defined in the formulae (2a) and (2b).
7. A composition according to claim 1, wherein the quaternary ammonium compound has the formula (1), in whichX1 is a halogen atom; —CH3SO4−; —C2H5SO4−; or —NO3−.
8. A composition according to claim 1, wherein in formula (1) A and B independently of one another are the radical of the formula (1a) or (1b).
9. A composition according to claim 8, wherein A and B are the radical of the formula (1b).
10. A composition according to claim 1, wherein the quaternary ammonium compound has the formula in whichR1, R2 and B are C1-C5alkyl; R3 is the aliphatic radical of tallow fatty acid; and X3− is a halogen atom.
11. A composition according to claim 1 comprising(a) a water-soluble phthalocyanine of the formula (b) a quaternary ammonium compound of the formula (8)
12. A composition according to claim 1 comprising(a) a water-soluble phthalocyanine of the formula (b) a quaternary ammonium compound of the formula
13. A composition according to claim 1, which comprisesfrom 0.0001 to 0.05% by weight of component (a) and from 1 to 20% by weight of component (b).
14. A process for the bleaching of textile fibre materials using a photobleaching agent, which comprises treating soiled textiles, after washing in a bath of a rinse-added fabric softener composition comprising(a) 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) phthalocyanine; and (b) a quaternary ammonium compound of the formula (1) as defined in claim 1, with irradiation with visible and/or infrared light or daylight, either in the fabric softener bath directly or on the damp textiles outside the fabric softener bath, and in the presence of oxygen.
15. A composition according to claim 1 which comprises a phthalocyanine of the formula in whichPC is the phthalocyanine ring system; R6 is a branched or unbranched C1-C8alkylene; or 1,3- or 1,4-phenylene; X2 is —NH—; or —N—C1-C5alkyl; X3+ is a group of the formula or, in the case where R6=C1-C8alkylene, also a group of the formula M is hydrogen, an alkali metal ion, ammonium ion or amine salt ion; and the sum of the numbers r1 and r2 is from 1 to 4 and As balances exactly the positive charge on the remainder of the molecule.

Priority Claims (1)

Number	Date	Country	Kind
97810573	Aug 1997	EP

Parent Case Info

This is a continuation of application Ser. No. 09/134,552, filed on Aug. 14, 1998, now abandoned.

US Referenced Citations (11)

Number	Name	Date	Kind
3927967	Speakman	Dec 1975	A
4033718	Holcombe et al.	Jul 1977	A
4094806	Wiers	Jun 1978	A
4166718	Reinert et al.	Sep 1979	A
4240920	de Luque	Dec 1980	A
4255273	Sakkab	Mar 1981	A
4368053	Eckhardt et al.	Jan 1983	A
4400173	Beavan	Aug 1983	A
5679661	Willey	Oct 1997	A
5744435	Hartman et al.	Apr 1998	A
5916481	Willey	Jun 1999	A

Foreign Referenced Citations (9)

Number	Date	Country
003371	Aug 1979	EP
3861	Sep 1979	EP
484027	Dec 1996	EP
4-108172	Apr 1992	JP
7-82591	Mar 1995	JP
9621714	Jul 1996	WO
WO 9621714	Jul 1996	WO
9705202	Feb 1997	WO
9705203	Feb 1997	WO

Continuations (1)

	Number	Date	Country
Parent	09/134552	Aug 1998	US
Child	09/618870		US

Fabric softener composition

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