EP1987122B1 - Shading dye granule its use in a detergent formulation and process to make it - Google Patents

Shading dye granule its use in a detergent formulation and process to make it Download PDF

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Publication number
EP1987122B1
EP1987122B1 EP07703298A EP07703298A EP1987122B1 EP 1987122 B1 EP1987122 B1 EP 1987122B1 EP 07703298 A EP07703298 A EP 07703298A EP 07703298 A EP07703298 A EP 07703298A EP 1987122 B1 EP1987122 B1 EP 1987122B1
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EP
European Patent Office
Prior art keywords
shading dye
granule
dye
shading
water
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Not-in-force
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EP07703298A
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German (de)
French (fr)
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EP1987122A1 (en
Inventor
Janette Cutrona
Tiago Ruiz Muniz
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Unilever PLC
Unilever NV
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Unilever PLC
Unilever NV
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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/046Salts
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0034Fixed on a solid conventional detergent ingredient
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/10Carbonates ; Bicarbonates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/10Salts
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/10Salts
    • C11D7/12Carbonates bicarbonates

Definitions

  • This invention relates to powdered laundry detergent compositions that include a shading dye or fabric substantive dye, it relates particularly to inclusion of a shading dye granule into an essentially uncoloured detergent composition.
  • White fabrics may be treated with dye in order to enhance whiteness.
  • the dye used is typically blue or violet. When these treated fabrics have been repeatedly washed with a detergent composition the dye may be removed from the fabric, leading to yellowing of the fabric.
  • WO 2005/003274 describes a laundry treatment composition which comprises a surfactant and from 0.0001 to 0.1 wt% of a combination of dyes which together have a visual effect on the human eye as a single dye having a peak absorption wavelength on cotton of from 540 nm to 650 nm, preferably from 570 nm to 630 nm, the combination comprising a photostable dye which is substantive to cotton.
  • a dye or combination of dyes may be referred to as a shading dye.
  • WO 2005/003275 teaches that such a shading dye may be incorporated into a treatment composition in a variety of ways. For example, dyes that are not sensitive to heat may be included in a slurry and spray dried. Alternatively the dye may be incorporated into granules that are post-dosed to a detergent powder. However, it has been found at higher concentrations of shading dye in the granules of this type that there could be a danger of spotting and dye damage on the clothes. WO 2005/003275 suggests that these problems may be avoided if the concentration of dye in the granules is less than 0.1 wt%.
  • Granules may be formed by loading an inorganic salt with soluble dye solution.
  • a problem with this is that the solution may leak from the granule when it is mixed with the remainder of the laundry detergent composition. This is especially likely if the composition is moist and/or warm: for example, during storage. The phenomenon of leaking of the dye into the surrounding composition is termed bleeding. It is a particularly significant problem for pale coloured or uncoloured detergent powder compositions.
  • Coloured granules containing a dye have also been used in detergent powder formulations as coloured speckles to provide visual cues. These granules or particles are large and contain as little dye as possible due to its non-functional nature. The dye is not fabric substantive and a shading dye is therefore unsuitable for this purpose.
  • EP 0336 635 describes a process for preparing a coloured granular alkali metal silicate. This is a visual cue type of speckle and uses a non-substantive dye. Non- substantive dyes may be incorporated at a higher level without fear of spotting damage if the dye granule comes into direct contact with a fabric.
  • the amount of colorant in the speckle granule should be low, so as not to interfere with the washing process.
  • the process involves spraying the inorganic material with dye or pigment and a solvent.
  • the silicate may be mixed with other inorganic materials such as zeolite, sodium sulphate or sodium phosphate.
  • the preferred particle size of the coloured granules is 0.8 to 1.6 mm.
  • the dye is suggested to be incorporated at a low level: 0.1 to 2 wt% of the granules and it is said to be present as a coating on the silicate.
  • WO 2000/27980 also relates to visible speckles.
  • the particle size being preferably 500 to 1440 mu m.
  • the speckle comprises a dye on a crystalline material that can be a hydrated salt, such as crystalline silicate.
  • the preferred level of dyestuff may be below 0.1 wt% of the speckle particle.
  • US 5073295 relates to coated granules containing, for example, soluble dyestuff.
  • the coatings provide excellent protection against decomposition and separation from other components., for example in detergent compositions.
  • the preferred particle size of the dye granules is 200 to 700 microns.
  • a granule for use as an additive in a laundry powder composition having a particle size distribution such that 90 wt% of the particles are less than 250 microns in diameter, the granule comprising 0.05 to 0.5 wt% shading dye solids absorbed into at least 80 wt% hydratable salt comprising light soda ash.
  • the salt may be used in admixture with zeolite in an amount of 0 to 20 wt%.
  • shading dye means one, or a combination of, water-soluble, photostable dyes, substantive to cotton, which, on cotton has a peak absorption wavelength of from 540nm to 650nm, preferably from 570nm to 630nm.
  • Such shading dyes are solid at room temperatures and are typically made into processable liquids by dissolving or dispersing in an aqueous medium.
  • quantities of shading dye mean the amount of shading dye solids and not the amount of shading dye solution or dispersion.
  • a method of manufacturing such a shading dye granule comprising the steps of dry mixing inorganic carrier materials comprising light soda ash and then spraying onto the mixture a liquid comprising shading dye and water.
  • Shading dye may be supplied as a dispersion or solution in water. It can be used as supplied or it can be further diluted by adding water. If it is used undiluted, care must be taken about the rate of addition of dye to the inorganic material. If it is used further diluted then the ratio of added water to shading dye solution should preferably be at least 2:1. Dilution of the shading dye with water enables a better control of the amount being added and aids dispersion of the dye over the inorganic solids.
  • the mixing and spraying preferably takes place in a drum mixer.
  • the amount of liquid sprayed on should be less than that which would lead to agglomeration of the inorganic carrier materials. This allows the retention of spare liquid carrying capacity in the inorganic.material. It has been found that by retaining at least 10% of the total liquid carrying capacity of the inorganic material the bleeding performance of the granule may be significantly improved.
  • zeolite is added after the initial mixing of the aqueous dye liquid and the inorganic carrier materials comprising light soda ash. It is also possible to spray the dye onto the zeolite and then dilute this mixture with inorganic salt.
  • a second problem with use of a highly loaded shading dye granule (or adjunct) is that it becomes visible against an uncoloured detergent powder, due to its contrasting colour. In this invention this is mitigated by preventing the agglomeration of shading dye containing particles during the manufacturing process. This is done by limiting the total amount of water and shading dye liquid to 15 wt%, preferably 10 wt%, of the amount of the inorganic salt carrier materials comprising light soda ash. As mentioned above, such a limitation also has the advantage that the salt is not fully loaded with diluted shading dye. This means that the bleeding problem is reduced. This is thought to be due to the ability of the shading dye liquid to expand on heating without being forced out of the shading dye granule. Use of these levels of liquid loading also avoids caking problems.
  • the concentration of shading dye (on a solids basis) in the liquid,sprayed on should not be greater than 25%, preferably not greater than 10%, most preferably not greater than 2.5%.
  • a typical range of shading dye concentration (solids basis) in the shading dye granule will be 0.05 to 0.4 wt% of the shading dye granule, preferably 0.07 to 0.27 wt%. It has been found that higher levels of shading dye lead to spotting damage if a fabric is left in contact with the powder.
  • lower concentrations of shading dye mean that too high a proportion of shading dye granules need to be added to a powder formulation to obtain the required level of shading dye inclusion in the total formulation. This, in turn, leads to bleeding of the shading dye into the formulation over time.
  • Typical levels of the shading dye granule in the powder formulation are in the range 0.1 to 2.0 wt%.
  • the granule can be used in conjunction with any laundry detergent powder formulations. It is especially useful for use with formulations that are white, or relatively lightly shaded, as these would have suffered particularly from any bleeding that occurs over time.
  • This test is designed to check if a powder containing a shading dye granule gives rise to staining and/or spotting of test fabrics.
  • This test checks shade colour change in finished powders containing shading dye granules.
  • a quantity of shading dye granules is incorporated into a standard detergent powder by mixing in a plastic bag. 30 grams of this product and a reference powder without any shading dye granules are stored in open petri dishes at 37°C/70%r.h. for 4 weeks.
  • a visual comparison against the reference is done weekly to check if any shade colour change is observed. Evaluation is carried out in a visual cabinet under daylight. The classification is: (Good): No, or very slight, bleeding observed. (Acceptable): Slight bleeding observed, but the shade colour change is still ok. (Rejected): Severe bleeding with clear shade colour change.
  • the shading dye used was an aqueous dispersion of the trisethoxy tripropanol-amine salt of Direct Violet 9. The salt was present at a concentration of about 10 wt% and was stabilised at this level in aqueous dispersion/solution by surfactant and other minor ingredients.
  • the water and dye were mixed together and sprayed onto the light soda ash in a low/medium shear batch mixer, with subsequent addition of zeolite towards the end of the batch.cycle. Except where specified otherwise the light soda ash used had 100wt% particles below 250 microns.
  • the shading dye granule of example 1 was added to a detergent powder, built with phosphate, at a level of 0.15 wt%. The appearance of the powder was not affected adversely by the incorporation of the shading dye granule.
  • the shading dye granule of example 2 was added to a zeolite built detergent powder formulation at a level of 0.5 wt%. The appearance of the powder was not affected adversely by the incorporation of the shading dye granule.
  • a shading dye granule was produced like example 1, except that a light soda ash with the following particle size was used:
  • a shading dye granule was produced like example 1, except that a light soda ash with the following particle size was used:
  • a shading dye granule was produced like example 1, except that a light soda ash with the following particle size was used:

Abstract

A shading dye granule for use as an additive in a laundry powder composition, the granule having a particle size distribution such that 90 wt% of the particles are less than 300 microns, preferably 250 microns, in diameter, the granule comprising: 0.05 to 0.5 wt% water soluble fabric substantive shading dye (solids) absorbed into at least 80 wt% hydratable salt.

Description

  • This invention relates to powdered laundry detergent compositions that include a shading dye or fabric substantive dye, it relates particularly to inclusion of a shading dye granule into an essentially uncoloured detergent composition.
  • White fabrics may be treated with dye in order to enhance whiteness. The dye used is typically blue or violet. When these treated fabrics have been repeatedly washed with a detergent composition the dye may be removed from the fabric, leading to yellowing of the fabric.
  • The prior art has suggested remedying this effect by delivering shading dye to the fabric during the laundry washing process. For example WO 2005/003274 describes a laundry treatment composition which comprises a surfactant and from 0.0001 to 0.1 wt% of a combination of dyes which together have a visual effect on the human eye as a single dye having a peak absorption wavelength on cotton of from 540 nm to 650 nm, preferably from 570 nm to 630 nm, the combination comprising a photostable dye which is substantive to cotton. Such a dye or combination of dyes may be referred to as a shading dye.
  • WO 2005/003275 teaches that such a shading dye may be incorporated into a treatment composition in a variety of ways. For example, dyes that are not sensitive to heat may be included in a slurry and spray dried. Alternatively the dye may be incorporated into granules that are post-dosed to a detergent powder. However, it has been found at higher concentrations of shading dye in the granules of this type that there could be a danger of spotting and dye damage on the clothes. WO 2005/003275 suggests that these problems may be avoided if the concentration of dye in the granules is less than 0.1 wt%.
  • Granules may be formed by loading an inorganic salt with soluble dye solution. A problem with this is that the solution may leak from the granule when it is mixed with the remainder of the laundry detergent composition. This is especially likely if the composition is moist and/or warm: for example, during storage. The phenomenon of leaking of the dye into the surrounding composition is termed bleeding. It is a particularly significant problem for pale coloured or uncoloured detergent powder compositions.
  • Coloured granules containing a dye have also been used in detergent powder formulations as coloured speckles to provide visual cues. These granules or particles are large and contain as little dye as possible due to its non-functional nature. The dye is not fabric substantive and a shading dye is therefore unsuitable for this purpose.
    EP 0336 635 describes a process for preparing a coloured granular alkali metal silicate. This is a visual cue type of speckle and uses a non-substantive dye. Non- substantive dyes may be incorporated at a higher level without fear of spotting damage if the dye granule comes into direct contact with a fabric. It is stated in this document that the amount of colorant in the speckle granule should be low, so as not to interfere with the washing process. The process involves spraying the inorganic material with dye or pigment and a solvent. It is taught that the silicate may be mixed with other inorganic materials such as zeolite, sodium sulphate or sodium phosphate. The preferred particle size of the coloured granules is 0.8 to 1.6 mm. The dye is suggested to be incorporated at a low level: 0.1 to 2 wt% of the granules and it is said to be present as a coating on the silicate.
  • WO 2000/27980 also relates to visible speckles. The particle size being preferably 500 to 1440 mu m. The speckle comprises a dye on a crystalline material that can be a hydrated salt, such as crystalline silicate. The preferred level of dyestuff may be below 0.1 wt% of the speckle particle.
  • US 5073295 relates to coated granules containing, for example, soluble dyestuff. The coatings provide excellent protection against decomposition and separation from other components., for example in detergent compositions. The preferred particle size of the dye granules is 200 to 700 microns.
  • According to the present invention there is provided a granule for use as an additive in a laundry powder composition, the granule having a particle size distribution such that 90 wt% of the particles are less than 250 microns in diameter, the granule comprising 0.05 to 0.5 wt% shading dye solids absorbed into at least 80 wt% hydratable salt comprising light soda ash.
  • The salt may be used in admixture with zeolite in an amount of 0 to 20 wt%.
  • In this specification "shading dye" means one, or a combination of, water-soluble, photostable dyes, substantive to cotton, which, on cotton has a peak absorption wavelength of from 540nm to 650nm, preferably from 570nm to 630nm. Such shading dyes are solid at room temperatures and are typically made into processable liquids by dissolving or dispersing in an aqueous medium. In this specification except in the examples references to quantities of shading dye mean the amount of shading dye solids and not the amount of shading dye solution or dispersion.
  • Also according to a second aspect of the present invention there is provided a method of manufacturing such a shading dye granule comprising the steps of dry mixing inorganic carrier materials comprising light soda ash and then spraying onto the mixture a liquid comprising shading dye and water. Shading dye may be supplied as a dispersion or solution in water. It can be used as supplied or it can be further diluted by adding water. If it is used undiluted, care must be taken about the rate of addition of dye to the inorganic material. If it is used further diluted then the ratio of added water to shading dye solution should preferably be at least 2:1. Dilution of the shading dye with water enables a better control of the amount being added and aids dispersion of the dye over the inorganic solids. The mixing and spraying preferably takes place in a drum mixer. The amount of liquid sprayed on should be less than that which would lead to agglomeration of the inorganic carrier materials. This allows the retention of spare liquid carrying capacity in the inorganic.material. It has been found that by retaining at least 10% of the total liquid carrying capacity of the inorganic material the bleeding performance of the granule may be significantly improved.
  • Advantageously zeolite is added after the initial mixing of the aqueous dye liquid and the inorganic carrier materials comprising light soda ash. It is also possible to spray the dye onto the zeolite and then dilute this mixture with inorganic salt.
  • A second problem with use of a highly loaded shading dye granule (or adjunct) is that it becomes visible against an uncoloured detergent powder, due to its contrasting colour. In this invention this is mitigated by preventing the agglomeration of shading dye containing particles during the manufacturing process. This is done by limiting the total amount of water and shading dye liquid to 15 wt%, preferably 10 wt%, of the amount of the inorganic salt carrier materials comprising light soda ash. As mentioned above, such a limitation also has the advantage that the salt is not fully loaded with diluted shading dye. This means that the bleeding problem is reduced. This is thought to be due to the ability of the shading dye liquid to expand on heating without being forced out of the shading dye granule. Use of these levels of liquid loading also avoids caking problems.
  • The concentration of shading dye (on a solids basis) in the liquid,sprayed on should not be greater than 25%, preferably not greater than 10%, most preferably not greater than 2.5%. Thus, a typical range of shading dye concentration (solids basis) in the shading dye granule will be 0.05 to 0.4 wt% of the shading dye granule, preferably 0.07 to 0.27 wt%. It has been found that higher levels of shading dye lead to spotting damage if a fabric is left in contact with the powder. On the other hand, lower concentrations of shading dye mean that too high a proportion of shading dye granules need to be added to a powder formulation to obtain the required level of shading dye inclusion in the total formulation. This, in turn, leads to bleeding of the shading dye into the formulation over time.
  • Typical levels of the shading dye granule in the powder formulation are in the range 0.1 to 2.0 wt%. The granule can be used in conjunction with any laundry detergent powder formulations. It is especially useful for use with formulations that are white, or relatively lightly shaded, as these would have suffered particularly from any bleeding that occurs over time.
  • It has also been found that the selection of the inorganic salt has an effect on the bleeding and spotting performance of the shading dye granules. Light soda ash is found to give the best results and has the required low particle size - less than about 10% above 250 microns. However; it would also be possible to.use magnesium sulphate, sodium tripolyphosphate, and zeolite in combination with sodium carbonate.
  • The invention will now be further described with reference to the following non-limiting examples. Two standard tests are carried out on the examples they are the Spotting test and the Bleeding test.
  • Spotting Test
  • This test is designed to check if a powder containing a shading dye granule gives rise to staining and/or spotting of test fabrics.
  • A load of a half T-shirts 100% Cotton (= 73 g) is added to a three litre bucket containing one litre of water. Three replicates of one monitor (15 x 15 cm) are placed in the bucket and 10 g of the test powder is spread over them. After 2 hours the monitors are removed and assessed visually for spotting damage. The damage is classified according to the following ranking scale:
    1. (1) - Very low damage
    2. (2) - Low damage
    3. (3) - Medium damage
    4. (4) - High damage
    5. (5) - Very high damage
    Bleeding Test
  • This test checks shade colour change in finished powders containing shading dye granules.
  • A quantity of shading dye granules is incorporated into a standard detergent powder by mixing in a plastic bag. 30 grams of this product and a reference powder without any shading dye granules are stored in open petri dishes at 37°C/70%r.h. for 4 weeks.
  • A visual comparison against the reference is done weekly to check if any shade colour change is observed. Evaluation is carried out in a visual cabinet under daylight. The classification is:
    (Good): No, or very slight, bleeding observed.
    (Acceptable): Slight bleeding observed, but the shade colour
    change is still ok.
    (Rejected): Severe bleeding with clear shade colour
    change.
  • Examples Example 1
  • A shading dye granule was manufactured with the ingredients shown below:
    Light soda ash = 89.0
    Zeolite 4A = 2.1
    Water = 8.15
    Shading dye = 0.75 (0.075 shading dye solids+water and stabilisers)
    The shading dye used was an aqueous dispersion of the trisethoxy tripropanol-amine salt of Direct Violet 9. The salt was present at a concentration of about 10 wt% and was stabilised at this level in aqueous dispersion/solution by surfactant and other minor ingredients. The water and dye were mixed together and sprayed onto the light soda ash in a low/medium shear batch mixer, with subsequent addition of zeolite towards the end of the batch.cycle. Except where specified otherwise the light soda ash used had 100wt% particles below 250 microns.
  • Example 2
  • A'shading dye granule was manufactured using a similar process to that used for example 1 with the ingredients shown below:
    Light soda ash = 53.1
    Sodium sulphate = 38.6
    Zeolite 4A = 1.2
    Water = 7.1
    Shading dye = 0.75 (0.075 shading dye solids + water + stabilisers)
    The shading dye was that same as that used in example 1. The water and dye were mixed together and sprayed onto the soda ash in a low/medium shear batch mixer, with subsequent addition of zeolite and then dilution with sodium sulphate towards the end of the batch cycle.
  • Example 3 (comparative)
  • A shading dye granule was manufactured in a high shear batch mixer using a similar process to that used for example 1, with the ingredients shown below:
    STPP anhydrous = 50.0
    Sodium sulphate = 47.0
    Water = 1.5
    Shading dye = 1.5 (0.15 shading dye solids + water + stabilisers)
    The shading dye was that same as that used in example 1. The water and dye were mixed together and sprayed onto STPP in a high shear batch mixer, with subsequent addition of sodium sulphate towards the end of the batch cycle.
  • Example 4 (comparative)
  • A shading dye granule was manufactured in a high shear batch mixer using a similar process used for example 3, with the ingredients shown below:
    Magnesium Sulphate = 85.0
    Water = 14.0
    Shading dye = 1.0 (0.1 shading dye solids + water + stabilisers)
  • Example 5
  • A shading dye granule was manufactured in a high shear batch mixer using a similar process to that used for example 1, with the ingredients shown below:
    Light soda ash = 76.0
    Zeolite 4A = 20.0
    Water = 3.0
    Shading dye = 1.0 (0.1 shading dye solids + water + stabilisers)
    The shading dye was the same as that used in example 1. The water and dye were mixed together and sprayed onto zeolite in a high shear batch mixer, with subsequent addition of light soda ash towards the end of the batch cycle.
  • Example 6
  • The shading dye granule of example 1 was added to a detergent powder, built with phosphate, at a level of 0.15 wt%. The appearance of the powder was not affected adversely by the incorporation of the shading dye granule.
  • Example 7
  • The shading dye granule of example 2 was added to a zeolite built detergent powder formulation at a level of 0.5 wt%. The appearance of the powder was not affected adversely by the incorporation of the shading dye granule.
  • Example 8
  • A shading dye granule was produced like example 1, except that a light soda ash with the following particle size was used:
    • 90 wt% below 250 microns
    • 10 wt% between 250-500 microns.
    Example 9 (comparative)
  • A shading dye granule was produced like example 1, except that a light soda ash with the following particle size was used:
    • 75 wt% below 250 microns
    • 25 wt% between 250-500 microns
    Example 10 (comparative)
  • A shading dye granule was produced like example 1, except that a light soda ash with the following particle size was used:
    • 40 wt% below 250 microns
    • 40 wt% between 250-500 microns
    • 20 wt% above 500 microns
  • The granules of examples 1, 2, 3, 4, 5, 8, 9 and 10 were assessed for spotting and bleeding. The results are given in table 1. Table 1
    Dye granule type Bleeding Spotting Ranking (1 to 5)
    Example 1 good 1
    Example 2 good 1
    Example 3 good 4
    Example 4 good 3
    Example 5 acceptable 1
    Example 8 good 2
    Example 9 good 3
    Example 10 good 5
    As can be seen from table 1 the use of the coarser grades of soda ash in comparative examples 9 and 10 leads to poorer spotting rankings.

Claims (4)

  1. A granule for use as an additive in a laundry powder composition, the granule having a particle size distribution such that 90 wt% of the particles are less than 250 microns, in diameter, the granule comprising: 0.05 to 0.5 wt% shading dye solids absorbed into at least 80 wt% hydratable salt wherein the hydratable salt comprises light soda ash and wherein shading dye is one or more water- soluble photostable dyes, substantive to cotton, and having a peak absorption wavelength on cotton of from 540 nm to 650 nm, preferably from 570 to 630 nm.
  2. A shading dye granule according to claim 1 wherein the granule further comprises sodium sulphate as hydratable salt.
  3. A detergent powder composition comprising 0.1 to 2.5 wt% of a shading dye granule according to any one of claims 1 or 2
  4. A process to manufacture a shading dye granule according to any one of claims 1 or 2 including the steps of:
    adding light soda ash to a low/medium shear mixer,
    optionally mixing aqueous shading dye solution with further water the ratio of water to shading dye solution being at least 2:1, and
    spraying the aqueous shading dye solution and optional further water mixture over the light soda ash while mixing, optionally adding further inorganic material with liquid carrying capacity, which may include further hydratable salt or zeolite, wherein agglomeration of the shading dye granules is prevented by using a total amount of water and shading dye solution of less than 15 wt%, preferably less than 10 wt%, of the weight of the granule produced.
EP07703298A 2006-02-25 2007-02-02 Shading dye granule its use in a detergent formulation and process to make it Not-in-force EP1987122B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP07703298A EP1987122B1 (en) 2006-02-25 2007-02-02 Shading dye granule its use in a detergent formulation and process to make it

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP06251020 2006-02-25
PCT/EP2007/000989 WO2007096052A1 (en) 2006-02-25 2007-02-02 Shading dye granule its use in a detergent formulation and process to make it
EP07703298A EP1987122B1 (en) 2006-02-25 2007-02-02 Shading dye granule its use in a detergent formulation and process to make it

Publications (2)

Publication Number Publication Date
EP1987122A1 EP1987122A1 (en) 2008-11-05
EP1987122B1 true EP1987122B1 (en) 2009-08-26

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EP07703298A Not-in-force EP1987122B1 (en) 2006-02-25 2007-02-02 Shading dye granule its use in a detergent formulation and process to make it

Country Status (7)

Country Link
EP (1) EP1987122B1 (en)
CN (1) CN101389742B (en)
AT (1) ATE440939T1 (en)
BR (1) BRPI0708269A2 (en)
DE (1) DE602007002165D1 (en)
WO (1) WO2007096052A1 (en)
ZA (1) ZA200807030B (en)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2084256B2 (en) * 2006-11-10 2017-03-29 The Procter and Gamble Company Fabric treatment composition with a fabric substantive dye
BRPI0821868A2 (en) * 2008-01-10 2015-07-28 Unilever Nv Granule
EP2206765A1 (en) 2009-01-08 2010-07-14 Unilever N.V. Detergent composition
EP2228429A1 (en) 2009-03-13 2010-09-15 Unilever PLC Shading dye and catalyst combination
US8318652B2 (en) 2009-08-25 2012-11-27 Milliken & Company Colored speckles comprising a porous carrier and a releasing agent layer
US8470760B2 (en) * 2010-05-28 2013-06-25 Milliken 7 Company Colored speckles for use in granular detergents
US20140371435A9 (en) 2011-06-03 2014-12-18 Eduardo Torres Laundry Care Compositions Containing Thiophene Azo Dyes
CA2867361C (en) 2012-03-19 2017-07-25 Milliken & Company Carboxylate dyes
EP3699256A1 (en) 2013-05-28 2020-08-26 The Procter & Gamble Company Surface treatment compositions comprising photochromic dyes
CN105555935A (en) 2013-09-18 2016-05-04 宝洁公司 Laundry care composition comprising carboxylate dye
JP6185182B2 (en) 2013-09-18 2017-08-23 ザ プロクター アンド ギャンブル カンパニー Laundry care composition containing a thiophene azocarboxylate dye
US9834682B2 (en) 2013-09-18 2017-12-05 Milliken & Company Laundry care composition comprising carboxylate dye
CN105555936A (en) 2013-09-18 2016-05-04 宝洁公司 Laundry care composition comprising carboxylate dye
EP3097172A1 (en) 2014-01-22 2016-11-30 The Procter & Gamble Company Method of treating textile fabrics
EP3097175B1 (en) 2014-01-22 2018-10-17 The Procter and Gamble Company Fabric treatment composition
WO2015112339A1 (en) 2014-01-22 2015-07-30 The Procter & Gamble Company Fabric treatment composition
EP3097174A1 (en) 2014-01-22 2016-11-30 The Procter & Gamble Company Method of treating textile fabrics
EP3140384B1 (en) 2014-05-06 2024-02-14 Milliken & Company Laundry care compositions
JP6866302B2 (en) 2015-05-04 2021-04-28 ミリケン・アンド・カンパニーMilliken & Company Leukotriphenylmethane dye as a bluish agent in laundry care compositions
US10308900B2 (en) * 2015-12-22 2019-06-04 Milliken & Company Occult particles for use in granular laundry care compositions
US20180119056A1 (en) 2016-11-03 2018-05-03 Milliken & Company Leuco Triphenylmethane Colorants As Bluing Agents in Laundry Care Compositions

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4961755A (en) * 1987-12-29 1990-10-09 Ciba-Geigy Corporation Coated active substances: dye coated with polyethylene oxide-propylene oxide or with ethoxylated stearyldi phenyloxyethyl diethylenetriamine
JPH01299898A (en) * 1988-03-30 1989-12-04 Unilever Nv Component for detergent composition
DE69914582T2 (en) * 1998-02-10 2004-08-05 Unilever N.V. TABLET DETERGENT
GB2343456A (en) * 1998-11-06 2000-05-10 Procter & Gamble Speckle particles and compositions containing the speckle particles
GB0314210D0 (en) * 2003-06-18 2003-07-23 Unilever Plc Laundry treatment compositions

Also Published As

Publication number Publication date
CN101389742A (en) 2009-03-18
WO2007096052A1 (en) 2007-08-30
ATE440939T1 (en) 2009-09-15
ZA200807030B (en) 2009-11-25
EP1987122A1 (en) 2008-11-05
CN101389742B (en) 2013-05-29
DE602007002165D1 (en) 2009-10-08
BRPI0708269A2 (en) 2011-06-07

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