WO2006128554A1 - Incorporation of antioxidant in detergent composition - Google Patents

Incorporation of antioxidant in detergent composition Download PDF

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Publication number
WO2006128554A1
WO2006128554A1 PCT/EP2006/004345 EP2006004345W WO2006128554A1 WO 2006128554 A1 WO2006128554 A1 WO 2006128554A1 EP 2006004345 W EP2006004345 W EP 2006004345W WO 2006128554 A1 WO2006128554 A1 WO 2006128554A1
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WIPO (PCT)
Prior art keywords
antioxidant
surfactant
bht
organic
organic surfactant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2006/004345
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French (fr)
Inventor
Renee Boerefijn
Andrew Paul Chapple
Bastiaan Domburg
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hindustan Unilever Ltd
Unilever NV
Original Assignee
Hindustan Lever Ltd
Hindustan Unilever Ltd
Unilever NV
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Application filed by Hindustan Lever Ltd, Hindustan Unilever Ltd, Unilever NV filed Critical Hindustan Lever Ltd
Priority to EP06742850A priority Critical patent/EP1885832B1/en
Priority to AT06742850T priority patent/ATE450594T1/en
Priority to MX2007015239A priority patent/MX2007015239A/en
Priority to BRPI0610944A priority patent/BRPI0610944B8/en
Priority to US11/921,379 priority patent/US20080318828A1/en
Priority to CN2006800190936A priority patent/CN101184833B/en
Priority to DE602006010851T priority patent/DE602006010851D1/en
Publication of WO2006128554A1 publication Critical patent/WO2006128554A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0084—Antioxidants; Free-radical scavengers
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/825—Mixtures of compounds all of which are non-ionic
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/83—Mixtures of non-ionic with anionic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2003—Alcohols; Phenols
    • C11D3/2006—Monohydric alcohols
    • C11D3/2034—Monohydric alcohols aromatic
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2093—Esters; Carbonates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/10—Objects to be cleaned
    • C11D2111/12—Soft surfaces, e.g. textile

Definitions

  • the present invention relates to a process for the incorporation of an antioxidant in a granular detergent composition, especially to the incorporation of BHT in a granular laundry detergent composition.
  • BHT 2,6 ditert-butyl-4-methyl phenol
  • Anti -oxidants such as BHT or propyl gallate are added to laundry detergent formulations to reduce or prevent the effects of oxidation processes. These effects can manifest themselves during storage or during use of the formulation.
  • Examples of the unwanted effects of oxidation processes are: malodour, discoloration, perfume degradation, deactivation of ingredients such as organic surfactants, bleach, enzymes and change in properties of rubber based materials.
  • Antioxidants are usually provided as water insoluble, non- dispersible solids. This poses a problem if they are to be dispersed efficiently in wash liquor in order to protect fabrics from oxidative effects.
  • BHT is soluble in ethanol . Use of ethanol in a detergent formulation is not ideal because of the volatility of ethanol.
  • One process used to incorporate BHT in laundry detergent compositions is by co- formulating it with a perfume.
  • this is a manufacturing constraint due to the fixed ratio of anti-oxidant -to perfume in such -a component-, which makes it difficult to vary the level of one ingredient independently of the other.
  • This fixed ratio results either in overdosing of one of the ingredients or in a larger number of the mixed ingredient raw materials having different ratios needing to be stocked.
  • It also has an impact on the types of perfume that may be used to avoid possible interaction of the perfume with the antioxidant; for example, BHT gives unwanted discoloration with some perfumes on storage. Combining antioxidant and perfume in this way may also cause problems for obtaining new sources of perfume. It is therefore desirable to seek other ways to incorporate antioxidants, especially BHT, in laundry detergent formulations.
  • Tinogard® (a BHT derivative) is incorporated into a detergent formation to reduce malodour.
  • the Tinogard® is added to the formulation by premixing it with zeolite.
  • BHT was added to a PAS formulation by two alternative processes.
  • the BHT was added to the base powder in the high-speed mixer/ granulator as a non-ionic surfactant/soap/BHT mixture.
  • the second alternative method it was post dosed in powder form. It was also suggested to add a dispersion or solution of antioxidant to the base powder by dissolving or dispersing it into a nonionic surfactant .
  • the postdosed method may be adapted to form granules on a carrier material with a binder. There is no suggestion to postdose the nonionic variant. This patent application is concerned with the problem of preventing oxidation of PAS at high temperatures during production.
  • a liquid detergent composition containing hydrogen peroxide is stabilised by addition of sterically hindered amines.
  • the compositions may contain surfactant and, in a comparative example, BHT is used. It is added to the liquid composition dissolved in nonionic surfactant (a Ci 3 -i 5 fatty alcohol ethoxylated with an average of 7 moles of ethylene oxide) .
  • nonionic surfactant a Ci 3 -i 5 fatty alcohol ethoxylated with an average of 7 moles of ethylene oxide
  • the amount of nonionic surfactant added is 0.5wt% of the full composition to deliver 0.02wt% BHT.
  • the loading of BHT in the nonionic surfactant is 4wt%.
  • a process for incorporation of up to 2% antioxidant into a granular detergent formulation comprising at least 5% organic surfactant includes the steps of
  • step a) dissolving the antioxidant in an organic surfactant selected from the group comprising anionic surfactant, nonionic surfactant and mixtures thereof, provided that the organic surfactant contains less than 5% by weight, preferably less than 3% by weight soap and most preferably is soap free; and b) adding the solution formed in step a) to the detergent formulation.
  • organic surfactant selected from the group comprising anionic surfactant, nonionic surfactant and mixtures thereof, provided that the organic surfactant contains less than 5% by weight, preferably less than 3% by weight soap and most preferably is soap free
  • the organic surfactant is preferably water free and highly saturated.
  • the organic surfactant used in step a) advantageously comprises less than 1% free water and furthermore it desirably " contains no ethylenic unsaturati-on-.
  • the surfactant is anionic or nonionic.
  • Nonionic surfactants are the most preferred due to these surfactants being commonly available in a water-free form.
  • Ethoxylated fatty alcohols are the preferred class of nonionic surfactants because of their ability to dissolve up to 40wt% of the antioxidant, particularly BHT. It is advantageous to dissolve at least 20wt% antioxidant into the surfactant so that to get a typical loading of 0.02wt% antioxidant into the granular detergent composition it is necessary to add as little as 0.05 and typically about 0. lwt%. of organic surfactant to the powder in the incorporation step.
  • the nonionic surfactant preferably has from 5 to 40 ethylene oxide units. It also preferably has from 8 to 45 carbon atoms in its backbone.
  • the ratio of surfactant to antioxidant in step a) is in the range 1000:1 to 1:1, preferably 10:1 to 2:1.
  • the antioxidant is preferably selected from the group comprising BHT and propyl gallate, most preferably BHT.
  • the organic surfactant may be pre-heated to assist in the dissolution of the antioxidant.
  • antioxidants also include free radical scavengers, except where the context would make this impossible.
  • Suitable free radical scavengers for use herein include the well-known " substituted mono ⁇ and drhydroxy benzenes -and- their analogs, alkyl and aryl carboxylates and mixtures thereof.
  • Preferred such radical scavengers for use herein include di- tert-butyl hydroxy toluene (BHT) , hydroquinone, ditert -butyl hydroquinone , mono-tert -butyl hydroquinone, tert-butyl- hydroxy anysole, benzoic acid, toluic acid, catechol, t- butyl catechol, benzylamine, 1 , 1 , 3-tris (2-methyl-4-hydrox-5- t-butylphenyl) butane, n-proyl-gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene.
  • BHT di- tert-butyl hydroxy to
  • radical scavengers like N-propyl-gallate may be commercially available from Nipa Laboratories under the trade name Nipanox SI®. Radical scavengers when used, are typically present herein in amounts ranging from up to 10% and preferably from 0.001% to 0.5% by weight of the total composition.
  • compositions made according to the invention may comprise further antioxidant or mixtures thereof.
  • Suitable further antioxidants to be used herein include organic acids like citric acid, ascorbic acid, tartaric acid, adipic acid and sorbic acid, or amines like lecithin, or amino acids like glutamine, methionine and cysteine, or esters like ascorbil palmitate, ascorbil stearate and triethylcitrate, or mixtures thereof.
  • Preferred antioxidants for use herein are citric acid, ascorbic acid, ascorbil palmitate, lecithin or mixtures thereof.
  • This manufacturing process has been shown to have the benefit of improving the efficacy of the anti-oxidant .
  • it can be used at a lower level to obtain the same efficacy or it can be used " at the " same level " to obtain even better protection of detergent ingredients and laundry.
  • the antioxidant can be dissolved into the surfactant easily during the detergent formulation manufacturing process, there is no longer the restriction of having to have two components like perfume and anti-oxidant in a fixed ratio. The only restriction is that there should be enough surfactant in the formulation to dissolve all the antioxidant.
  • the minimum level is a 2:1 weight excess over the antioxidant although it is possible to dissolve up to 40wt% BHT in some surfactants.
  • surfactant it is preferred for the surfactant to be selected from those already present in the formulation. However, an additional surfactant may also be employed. Incorporation of BHT by dissolution in nonionic has been found to give particularly good protection of rubber based materials from catalysed oxidation systems during the wash.
  • a granular laundry detergent comprising an antioxidant dissolved in ethoxylated nonionic surfactant to confer improved deposition of the antioxidant onto rubber during a wash process.
  • a preferred process for manufacture of a powdered detergent formulation is to add the antioxidant in a nonionic surfactant by spraying this mixture onto the powder whilst the powder is being mixed.
  • a drum mixer or other suitable process may be used to perform this method of incorporation.
  • Suitable alternative mixers- include f-lu-idised beds and double cone mixers.
  • the granular laundry detergent formulation, or powder is not limited: provided it contains organic surfactant. It may comprise mixtures of organic surfactants such as anionic and nonionic surfactant. It may comprise builders and other ingredients commonly found in detergent powder formulations.
  • the composition may be low medium or high bulk density and may be produced by any of the processes known in the art .
  • BHT was dissolved in a C12-15 fatty alcohol nonionic surfactant ethoxylated with an average of 7 moles of ethylene oxide. It was found possible to dissolve up to 40wt% of BHT in the organic surfactant. In a variant of this procedure it was found easily possible to dissolve 30 wt% of the antioxidant in Synperonic A05 nonionic surfactant.
  • Example 3 A 30wt% solution of BHT in nonionic organic surfactant as described in example 1 was sprayed in a drum mixer onto a phosphate built granular detergent composition containing LAS as anionic surfactant in an amount so as to give 0.02wt% of -BHT in the finished granular detergent. Because so little nonionic surfactant was added in this way there was no need for any further process operation.
  • Example 3 A 30wt% solution of BHT in nonionic organic surfactant as described in example 1 was sprayed in a drum mixer onto a phosphate built granular detergent composition containing LAS as anionic surfactant in an amount so as to give 0.02wt% of -BHT in the finished granular detergent. Because so little nonionic surfactant was added in this way there was no need for any further process operation.
  • Example 3 A 30wt% solution of BHT in nonionic organic surfactant as described in example 1 was sprayed in a drum mixer onto a phosphate built gran
  • Control A Laundry powder without BHT
  • Control B Laundry powder with 0.02% BHT added in perfume
  • Example 4 Laundry powder with 0.02% BHT added in nonionic surfactant as described in example 2.
  • the BHT was supplied by Fluka .
  • Test 1 the formulations used for Test 1 were used to wash rubber-based materials eight times each. BHT was then extracted from the material to see how much had been absorbed or deposited during the 8 washes, using the value for Example A as the base line. The results are given in Table 2.

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Abstract

A process for incorporation of up to 2% antioxidant into a granular detergent formulation comprising at least 5% organic surfactant, including the steps of: a) dissolving the antioxidant in an organic surfactant selected from the group comprising anionic surfactant, nonionic surfactant and mixtures thereof, provided that the organic surfactant contains less than 5% by weight, preferably less than 3% by weight soap and most preferably is soap free; and b) adding the solution formed in step a) to the detergent formulation and use of the granular laundry detergent composition to confer improved deposition of the antioxidant onto rubber during a wash process.

Description

INCORPORATION OF ANTIOXIDANT IN DETERGENT COMPOSITION
The present invention relates to a process for the incorporation of an antioxidant in a granular detergent composition, especially to the incorporation of BHT in a granular laundry detergent composition.
BHT (2,6 ditert-butyl-4-methyl phenol) is an antioxidant.
Anti -oxidants such as BHT or propyl gallate are added to laundry detergent formulations to reduce or prevent the effects of oxidation processes. These effects can manifest themselves during storage or during use of the formulation.
Examples of the unwanted effects of oxidation processes are: malodour, discoloration, perfume degradation, deactivation of ingredients such as organic surfactants, bleach, enzymes and change in properties of rubber based materials.
Antioxidants are usually provided as water insoluble, non- dispersible solids. This poses a problem if they are to be dispersed efficiently in wash liquor in order to protect fabrics from oxidative effects. BHT is soluble in ethanol . Use of ethanol in a detergent formulation is not ideal because of the volatility of ethanol.
One process used to incorporate BHT in laundry detergent compositions is by co- formulating it with a perfume. However, this is a manufacturing constraint due to the fixed ratio of anti-oxidant -to perfume in such -a component-, which makes it difficult to vary the level of one ingredient independently of the other. This fixed ratio results either in overdosing of one of the ingredients or in a larger number of the mixed ingredient raw materials having different ratios needing to be stocked. It also has an impact on the types of perfume that may be used to avoid possible interaction of the perfume with the antioxidant; for example, BHT gives unwanted discoloration with some perfumes on storage. Combining antioxidant and perfume in this way may also cause problems for obtaining new sources of perfume. It is therefore desirable to seek other ways to incorporate antioxidants, especially BHT, in laundry detergent formulations.
In WO2005054422 Tinogard® (a BHT derivative) is incorporated into a detergent formation to reduce malodour. The Tinogard® is added to the formulation by premixing it with zeolite.
In WO9606151 BHT was added to a PAS formulation by two alternative processes. In the preferred process, the BHT was added to the base powder in the high-speed mixer/ granulator as a non-ionic surfactant/soap/BHT mixture. In the second alternative method it was post dosed in powder form. It was also suggested to add a dispersion or solution of antioxidant to the base powder by dissolving or dispersing it into a nonionic surfactant . Alternatively, the postdosed method may be adapted to form granules on a carrier material with a binder. There is no suggestion to postdose the nonionic variant. This patent application is concerned with the problem of preventing oxidation of PAS at high temperatures during production. Hence, the preference to add the antioxidant to the base powder and to post dose after the antioxidant is present. In EP 1302 442 a liquid detergent composition containing hydrogen peroxide is stabilised by addition of sterically hindered amines. The compositions may contain surfactant and, in a comparative example, BHT is used. It is added to the liquid composition dissolved in nonionic surfactant (a Ci3-i5 fatty alcohol ethoxylated with an average of 7 moles of ethylene oxide) . The amount of nonionic surfactant added is 0.5wt% of the full composition to deliver 0.02wt% BHT. Thus, the loading of BHT in the nonionic surfactant is 4wt%.
According to the present invention a process for incorporation of up to 2% antioxidant into a granular detergent formulation comprising at least 5% organic surfactant, includes the steps of
a) dissolving the antioxidant in an organic surfactant selected from the group comprising anionic surfactant, nonionic surfactant and mixtures thereof, provided that the organic surfactant contains less than 5% by weight, preferably less than 3% by weight soap and most preferably is soap free; and b) adding the solution formed in step a) to the detergent formulation.
The organic surfactant is preferably water free and highly saturated. The organic surfactant used in step a) advantageously comprises less than 1% free water and furthermore it desirably" contains no ethylenic unsaturati-on-.
More preferably, the surfactant is anionic or nonionic. Nonionic surfactants are the most preferred due to these surfactants being commonly available in a water-free form. Ethoxylated fatty alcohols are the preferred class of nonionic surfactants because of their ability to dissolve up to 40wt% of the antioxidant, particularly BHT. It is advantageous to dissolve at least 20wt% antioxidant into the surfactant so that to get a typical loading of 0.02wt% antioxidant into the granular detergent composition it is necessary to add as little as 0.05 and typically about 0. lwt%. of organic surfactant to the powder in the incorporation step. The nonionic surfactant preferably has from 5 to 40 ethylene oxide units. It also preferably has from 8 to 45 carbon atoms in its backbone.
The ratio of surfactant to antioxidant in step a) is in the range 1000:1 to 1:1, preferably 10:1 to 2:1.
The antioxidant is preferably selected from the group comprising BHT and propyl gallate, most preferably BHT.
The organic surfactant may be pre-heated to assist in the dissolution of the antioxidant.
Throughout this specification references to antioxidants also include free radical scavengers, except where the context would make this impossible.
Suitable free radical scavengers for use herein include the well-known"substituted mono^ and drhydroxy benzenes -and- their analogs, alkyl and aryl carboxylates and mixtures thereof. Preferred such radical scavengers for use herein include di- tert-butyl hydroxy toluene (BHT) , hydroquinone, ditert -butyl hydroquinone , mono-tert -butyl hydroquinone, tert-butyl- hydroxy anysole, benzoic acid, toluic acid, catechol, t- butyl catechol, benzylamine, 1 , 1 , 3-tris (2-methyl-4-hydrox-5- t-butylphenyl) butane, n-proyl-gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene. Such radical scavengers like N-propyl-gallate may be commercially available from Nipa Laboratories under the trade name Nipanox SI®. Radical scavengers when used, are typically present herein in amounts ranging from up to 10% and preferably from 0.001% to 0.5% by weight of the total composition.
The compositions made according to the invention may comprise further antioxidant or mixtures thereof.
Suitable further antioxidants to be used herein include organic acids like citric acid, ascorbic acid, tartaric acid, adipic acid and sorbic acid, or amines like lecithin, or amino acids like glutamine, methionine and cysteine, or esters like ascorbil palmitate, ascorbil stearate and triethylcitrate, or mixtures thereof. Preferred antioxidants for use herein are citric acid, ascorbic acid, ascorbil palmitate, lecithin or mixtures thereof.
This manufacturing process has been shown to have the benefit of improving the efficacy of the anti-oxidant . Thus it can be used at a lower level to obtain the same efficacy or it can be used" at the "same level" to obtain even better protection of detergent ingredients and laundry. Furthermore, because the antioxidant can be dissolved into the surfactant easily during the detergent formulation manufacturing process, there is no longer the restriction of having to have two components like perfume and anti-oxidant in a fixed ratio. The only restriction is that there should be enough surfactant in the formulation to dissolve all the antioxidant. Typically, for nonionic surfactant, the minimum level is a 2:1 weight excess over the antioxidant although it is possible to dissolve up to 40wt% BHT in some surfactants. It is preferred for the surfactant to be selected from those already present in the formulation. However, an additional surfactant may also be employed. Incorporation of BHT by dissolution in nonionic has been found to give particularly good protection of rubber based materials from catalysed oxidation systems during the wash.
According to a second aspect of the invention there is provided the use of a granular laundry detergent comprising an antioxidant dissolved in ethoxylated nonionic surfactant to confer improved deposition of the antioxidant onto rubber during a wash process.
A preferred process for manufacture of a powdered detergent formulation is to add the antioxidant in a nonionic surfactant by spraying this mixture onto the powder whilst the powder is being mixed. A drum mixer or other suitable process may be used to perform this method of incorporation. Suitable alternative mixers- include f-lu-idised beds and double cone mixers. The granular laundry detergent formulation, or powder, is not limited: provided it contains organic surfactant. It may comprise mixtures of organic surfactants such as anionic and nonionic surfactant. It may comprise builders and other ingredients commonly found in detergent powder formulations. The composition may be low medium or high bulk density and may be produced by any of the processes known in the art .
The invention will now be further described with reference to the following non-limiting examples.
Example 1
BHT was dissolved in a C12-15 fatty alcohol nonionic surfactant ethoxylated with an average of 7 moles of ethylene oxide. It was found possible to dissolve up to 40wt% of BHT in the organic surfactant. In a variant of this procedure it was found easily possible to dissolve 30 wt% of the antioxidant in Synperonic A05 nonionic surfactant.
Example 2
A 30wt% solution of BHT in nonionic organic surfactant as described in example 1 was sprayed in a drum mixer onto a phosphate built granular detergent composition containing LAS as anionic surfactant in an amount so as to give 0.02wt% of -BHT in the finished granular detergent. Because so little nonionic surfactant was added in this way there was no need for any further process operation. Example 3
Control A: Laundry powder without BHT
Control B: Laundry powder with 0.02% BHT added in perfume
Example 4: Laundry powder with 0.02% BHT added in nonionic surfactant as described in example 2. The BHT was supplied by Fluka .
Two tests were carried out.
Test 1
In this test, we investigated the effect of the method of incorporation of the BHT on the quantity of BHT found in the wash liquor. This test indicates how well the composition stores and then disperses the BHT into solution. Analysis is done by means of ABTS. In each case, the wash liquor is made up using 6FH water. ABTS reaction times of 15 mins on solutions were used.
The results are shown in table 1 below:
Table 1
Figure imgf000009_0001
Comparison of the perfume route (B) with the nonionic route (4) shows much better availability of the BHT in the wash when added via the nonionic. NB that due to solubility constraints the wt% BHT in the perfume could only be about 6 wt% maximum. Thus, the amount of spray on needed to be much larger for example B than for example 4.
Test 2
For this test, the formulations used for Test 1 were used to wash rubber-based materials eight times each. BHT was then extracted from the material to see how much had been absorbed or deposited during the 8 washes, using the value for Example A as the base line. The results are given in Table 2.
Table 2
Figure imgf000010_0001
It can be seen that the most effective process for incorporation is the process according to the invention - example 4. The use of the perfume process is clearly not as effective as the use of non-ionic surfactant .

Claims

1. A process for incorporation of up to 2% antioxidant into a granular detergent formulation comprising at least 5% organic surfactant, including the steps of
c) dissolving the antioxidant in an organic surfactant selected from the group comprising anionic surfactant, nonionic surfactant and mixtures thereof, provided that the organic surfactant contains less than 5% by weight, preferably less than 3% by weight soap and most preferably is soap free; and d) adding the solution formed in step a) to the detergent formulation.
2. A process as claimed in claim 1 wherein the organic surfactant used in step a) comprises less than 1% free water.
3. A process as claimed in claim 1 or claim 2 wherein the organic surfactant used in step a) contains no ethylenic unsaturation.
4. A process as claimed in claim 3 wherein the organic surfactant is a nonionic surfactant.
5". A" process as claimed in -claim- 4 wherein the- non-ionie- surfactant has from 5 to 40 ethylene oxide units.
6. A process as claimed in claim 5 wherein the nonionic surfactant has from 8 to 45 carbon atoms in its backbone .
7. A process as claimed in any preceding claim in which the organic surfactant is heated to dissolve the antioxidant .
8. A process as claimed in any preceding claim in which the antioxidant is selected from the group comprising
BHT and propyl gallate, preferably BHT.
9. A process as claimed in any preceding claim in which the ratio of surfactant to antioxidant in step a) is in the range 1000:1 to 1:1, preferably 10:1 to 2:1.
10. Use of a granular laundry detergent composition comprising an antioxidant dissolved in ethoxylated nonionic surfactant to confer improved deposition of the antioxidant onto rubber during a wash process.
PCT/EP2006/004345 2005-06-03 2006-05-01 Incorporation of antioxidant in detergent composition Ceased WO2006128554A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP06742850A EP1885832B1 (en) 2005-06-03 2006-05-01 Incorporation of antioxidant in detergent composition
AT06742850T ATE450594T1 (en) 2005-06-03 2006-05-01 ADDITION OF ANTIOXIDANT TO DETERGENT
MX2007015239A MX2007015239A (en) 2005-06-03 2006-05-01 Incorporation of antioxidant in detergent composition.
BRPI0610944A BRPI0610944B8 (en) 2005-06-03 2006-05-01 process for incorporating antioxidant into a granular detergent composition and the use
US11/921,379 US20080318828A1 (en) 2005-06-03 2006-05-01 Incorporation of Antioxidant in Detergent Composition
CN2006800190936A CN101184833B (en) 2005-06-03 2006-05-01 Incorporation of antioxidant in detergent composition
DE602006010851T DE602006010851D1 (en) 2005-06-03 2006-05-01 ADDITION OF ANTIOXIDANT TO DETERGENT

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GBGB0511313.9A GB0511313D0 (en) 2005-06-03 2005-06-03 Incorporation of antioxidant in detergent composition
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DE102009028891A1 (en) 2009-08-26 2011-03-03 Henkel Ag & Co. Kgaa Improved washing performance by free radical scavengers
CN105018246A (en) * 2015-07-10 2015-11-04 山东妙凌生物药业有限公司 Mildewproof oxidation-resistant laundry detergent

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CA3106528A1 (en) 2018-07-27 2020-01-30 The Procter & Gamble Company Leuco colorants as bluing agents in laundry care compositions
CN110452790A (en) * 2019-08-27 2019-11-15 如皋市涤诺皂业有限公司 A kind of Thief zone high activity object liquid detergent and preparation method thereof
US11802259B2 (en) * 2019-11-08 2023-10-31 The Procter & Gamble Company Process of reducing malodors on fabrics
WO2025064739A1 (en) * 2023-09-22 2025-03-27 The Procter & Gamble Company Water-soluble unit dose article comprising a phosphonate-free chelating agent

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WO1996006151A1 (en) * 1994-08-24 1996-02-29 Unilever Plc Detergent compositions

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DE102009028891A1 (en) 2009-08-26 2011-03-03 Henkel Ag & Co. Kgaa Improved washing performance by free radical scavengers
WO2011023716A1 (en) 2009-08-26 2011-03-03 Henkel Ag & Co. Kgaa Improved washing performance using radical traps
CN105018246A (en) * 2015-07-10 2015-11-04 山东妙凌生物药业有限公司 Mildewproof oxidation-resistant laundry detergent
CN105018246B (en) * 2015-07-10 2018-11-02 山东妙凌生物药业有限公司 A kind of mold-proof oxidation-resistant liquid detergent

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DE602006010851D1 (en) 2010-01-14
ATE450594T1 (en) 2009-12-15
US20080318828A1 (en) 2008-12-25
ZA200709685B (en) 2009-04-29
CN101184833A (en) 2008-05-21
EP1885832B1 (en) 2009-12-02
BRPI0610944B1 (en) 2016-10-25
CN101184833B (en) 2011-11-09
GB0511313D0 (en) 2005-07-13
EP1885832A1 (en) 2008-02-13
BRPI0610944A2 (en) 2010-08-03
MX2007015239A (en) 2008-02-22

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