EP0447261A1 - Bleaching composition - Google Patents

Bleaching composition Download PDF

Info

Publication number
EP0447261A1
EP0447261A1 EP19910302262 EP91302262A EP0447261A1 EP 0447261 A1 EP0447261 A1 EP 0447261A1 EP 19910302262 EP19910302262 EP 19910302262 EP 91302262 A EP91302262 A EP 91302262A EP 0447261 A1 EP0447261 A1 EP 0447261A1
Authority
EP
European Patent Office
Prior art keywords
amount
soap
carbon atoms
composition
solution according
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.)
Granted
Application number
EP19910302262
Other languages
German (de)
French (fr)
Other versions
EP0447261B1 (en
Inventor
Christophe Joyeux
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.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10672693&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0447261(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Publication of EP0447261A1 publication Critical patent/EP0447261A1/en
Application granted granted Critical
Publication of EP0447261B1 publication Critical patent/EP0447261B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C11D3/395Bleaching agents
    • C11D3/3956Liquid compositions
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/37Mixtures of compounds all of which are anionic
    • 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • C11D10/042Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on anionic surface-active compounds and soap
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides

Definitions

  • This invention relates to hypochlorite-based aqueous liquid bleaching compositions.
  • hypochlorite bleach It is well known to include both hypochlorite bleach and surfactant in the same compositions.
  • alkyl ether sulphate and/or soap in surfactants present enhances the ability of the composition to dissolve perfume.
  • the incorporation of perfume is generally desired for compositions intended for domestic use.
  • incorporation of some alkyl ether sulphate can improve the ability of the composition to remove a number of stains.
  • a perfumed aqueous liquid solution of alkali metal hypochlorite also containing a surfactant mixture comprising
  • alkali metal hypochlorite solution contains varying amounts of sodium chloride. We prefer to use hypochlorite solution which has a fairly low content of sodium chloride. We have then found it possible to prepare compositions which contain a substantial proportion of surfactant.
  • compositions of the invention are devoid of hydrotropes such as urea, alcohols with up to four carbon atoms, or short chain alkylaryl sulphonates, e.g.
  • the proportion by weight of it may be less than the amount of surfactants (other than amine oxide, if any) present, better less than half the amount of surfactants other than amine oxide. In any case, it is desirable to exclude urea and primary or secondary alcohols because these are not stable in the presence of hypochlorite.
  • the alkane sulphonate used in this invention has the formula: R - SO3M where R is an alkyl group of 8 to 22.
  • R has 12 to 22, carbon atoms and the solubilising cation M is preferably alkali metal.
  • R is a secondary alkyl group. It may be branched but preferably is unbranched.
  • the amount of the alkane sulphonate lies in the range from 1 to 10% by weight of the composition.
  • the amount may possibly be not more than 8%, e.g. 2% to 6%.
  • Alkyl ether sulphate useful in this invention has the formula: R1 - (OC2H4) n OSO3M where M is a solubilising cation, especially alkali metal, R1 is an alkyl group of 8 to 20, preferably 10 to 16, carbon atoms and n has an average value in the range from 0.5 to 12, better 1 to 6, even better 2 to 5. R1 may be primary or secondary, and preferably is unbranched.
  • Soap useful in this invention has the formula: R2CO2M where M is a solubilising cation, especially alkali metal and R2 is an alkyl group of 7 to 19, preferably 9 to 15, carbon atoms. Olefinic unsaturation should desirably be absent, for the sake of stability in the presence of hypochlorite.
  • the total amount of soap and alkyl ether sulphate lies in the range from 0.1, preferably 0.2, to 4% by weight of the composition. If alkyl ether sulphate is present, the amount will generally be at least 0.1% by weight. Similarly, if soap is present, the amount will generally be at least 0.1%.
  • the weight ratio of alkane sulphonate to the total of alkyl ether sulphate and soap is preferably from 1:1 to 10:1 better 2:1 to 6:1.
  • R, R1 and R2 can, but do not need to be, the same, but preferably R1 and R2CO2 both have an average carbon chain length of 10 to 16 carbon atoms and may be predominantly of 12 carbon length.
  • hypochlorite is desirably included in a quantity to provide from 0.1 to 8%, better 0.5 to 3% or 5% of available chlorine, by weight based on the whole composition. It is desirable to use hypochlorite in which the amount of available chlorine is at least twice the amount of any sodium chloride present.
  • One supplier of suitable hypochlorite is Tahn and Mulhouse.
  • the composition will generally be alkaline.
  • alkali metal hydroxide may be included in a quantity between 0.1 and 1.5% by weight of the composition.
  • the amount of perfume dissolved in the composition, made soluble by the presence of alkyl ether sulphate and/or soap may lie in the range from 0.1 to 1.0% by weight of the composition.
  • the amount of perfume is up to 0.6 or 0.7%.
  • a preferred composition according to this invention may have constituents and quantities as set out below.
  • alkali metal silicate a constituent that is possible. Notable is 0.1 to 0.5% of alkali metal silicate.
  • the pH of the composition is, suitably, greater than 11. This will give a lesser alkaline pH on dilution, especially when dilution is with hard tap water.
  • compositions were prepared using the following constituents: Secondary alkane sulphonate (SAS) with average 16-18 carbon atoms Linear alkyl ether sulphate (LES) in which the alkyl group has average 12-13 carbon atoms and the average degree of ethoxylation is 3 Lauric soap Sodium hydroxide Perfume
  • compositions were made up in distilled water. All compositions contained sufficient hypochlorite to yield 1% available chlorine. It was noted whether the compositions were cloudy or clear. Compositions and results are set out in the following Tables 1 and 2:
  • compositions 2, 3 and 4 show that increasing the amount of SAS from 2.0 to 2.8% was not sufficient to render the perfume soluble but addition of 0.26% soap did bring about solution of the perfume.
  • Composition 12 shows that addition of 0.26% LES also brought about solution of the perfume.
  • Compositions 5, 6 and 7 show the same effect at higher concentrations. Increasing the SAS level to 2.0 to 3.9% was not enough to bring about solution of 0.3% perfume but addition of 0.58% soap did cause the perfume to dissolve.
  • compositions 8 and 9 show that increasing the level of SAS to 5% was not enough to bring about the solution of perfume. Comparison also with compositions 10 and 11 shows that addition of 0.5% LES or 0.5% soap did dissolve the perfume.
  • compositions were prepared using the same constituents as in Example 1, although in addition all compositions included 0.2% sodium silicate. Compositions and results are set out in the following Table 3.
  • compositions 15, 16, 18 and 20 demonstrate that soap and LES can be used together to bring about the solubilisation of perfume.
  • compositions were prepared using the same materials as in Example 1, without sodium silicate, and with the amounts of the materials as set out in the following Table 4.
  • compositions were prepared in distilled water using the same materials as in Example 1 without sodium silicate, and with the amounts of the materials as set out in the following Table 5.
  • compositions were used to remove various stains by a standard procedure. 1 ml of the composition was applied to a plastic tile bearing the stain. The tile was rubbed with the composition 200 times, using a machine to rub the tile. Each composition was used to clean three tiles bearing each stain. After the tiles had been cleaned in this way the effectiveness of cleaning was assessed by a panel of five evaluators whose assessments were averaged.
  • Composition D was found to be more effective than C on stains which were oil, two types of glue, vegetable fat and red pencil.
  • compositions of Example 2 were diluted with distilled water and used to wash a plastic tile. This was allowed to dry and the presence of streaks on the tile was assessed by the panel of evaluators.
  • the amounts of composition diluted to one litre with water were 20, 25 and 50 grams. At each dilution composition D gave less streaking than composition C.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Fats And Perfumes (AREA)

Abstract

A bleaching composition is a perfumed aqueous solution of alkali metal hypochlorite containing alkane sulphonate with alkyl ether sulphate and/or soap. Amine oxide and hydrotropes are unnecessary and the amount of amine oxide (if any) is limited to half the amount of other surfactants.

Description

  • This invention relates to hypochlorite-based aqueous liquid bleaching compositions.
  • It is well known to include both hypochlorite bleach and surfactant in the same compositions.
  • We have now found that useful properties, in particular useful combinations of properties, can be obtained using a mixture of specified anionic surfactants.
  • We have found that including alkyl ether sulphate and/or soap in surfactants present enhances the ability of the composition to dissolve perfume. Of course the incorporation of perfume is generally desired for compositions intended for domestic use. We have also found that incorporation of some alkyl ether sulphate can improve the ability of the composition to remove a number of stains.
  • According to this invention there is provided a perfumed aqueous liquid solution of alkali metal hypochlorite, also containing a surfactant mixture comprising
    • (i) an alkane sulphonate of formula R-SO₃M in which R is an alkyl group with 8 to 22 carbon atoms and either
    • (ii) an alkyl ether sulphate of formula R¹-(OC₂H₄)n SO₄M in which R¹ is an alkyl group with 8 to 20 carbon atoms and n has a value in the range from 0.5 to 12, and/or
    • (iii) soap of formula R²CO₂M where R² is an alkyl or alkenyl group of 7 to 19 carbon atoms,
         each M denoting a solubilising cation;
         the amounts of the said surfactants, by weight based on the whole composition, being
    • i) alkane sulphonate   1 to 10%
    • ii) alkyl ether sulphate   0 to 3%
    • iii) soap   0 to 3%
         but the total of (ii) and (iii) being 0.1 to 4%, the amount of amine oxide (if any) in the composition being less than half the content of other surfactants.
  • Commercial supplies of alkali metal hypochlorite solution contain varying amounts of sodium chloride. We prefer to use hypochlorite solution which has a fairly low content of sodium chloride. We have then found it possible to prepare compositions which contain a substantial proportion of surfactant.
  • One category of surfactant which has been used extensively for (thickened) hypochlorite compositions is the amine oxides. The use of these is discussed in our UK patent 1329086 which explains that the amine oxides can function like a hydrotrope (although they are normally regarded as surfactants). We have found it unnecessary to include amine oxide or hydrotrope. It is a feature of this invention that the proportion by weight of any amine oxide is less than half the amount of other surfactant. Preferably amine oxide is entirely absent. It is also preferred that compositions of the invention are devoid of hydrotropes such as urea, alcohols with up to four carbon atoms, or short chain alkylaryl sulphonates, e.g. with no more than four carbon atoms in the alkyl group(s). If any such hydrotrope is present, the proportion by weight of it may be less than the amount of surfactants (other than amine oxide, if any) present, better less than half the amount of surfactants other than amine oxide. In any case, it is desirable to exclude urea and primary or secondary alcohols because these are not stable in the presence of hypochlorite.
  • The alkane sulphonate used in this invention has the formula: R - SO₃M
    Figure imgb0001
    where R is an alkyl group of 8 to 22. Preferably R has 12 to 22, carbon atoms and the solubilising cation M is preferably alkali metal. Preferably R is a secondary alkyl group. It may be branched but preferably is unbranched.
  • The amount of the alkane sulphonate lies in the range from 1 to 10% by weight of the composition. The amount may possibly be not more than 8%, e.g. 2% to 6%.
  • Alkyl ether sulphate useful in this invention has the formula: R¹ - (OC₂H₄) n OSO₃M
    Figure imgb0002
    where M is a solubilising cation, especially alkali metal, R¹ is an alkyl group of 8 to 20, preferably 10 to 16, carbon atoms and n has an average value in the range from 0.5 to 12, better 1 to 6, even better 2 to 5. R¹ may be primary or secondary, and preferably is unbranched.
  • Soap useful in this invention has the formula: R²CO₂M
    Figure imgb0003
    where M is a solubilising cation, especially alkali metal and R² is an alkyl group of 7 to 19, preferably 9 to 15, carbon atoms. Olefinic unsaturation should desirably be absent, for the sake of stability in the presence of hypochlorite.
  • The total amount of soap and alkyl ether sulphate lies in the range from 0.1, preferably 0.2, to 4% by weight of the composition. If alkyl ether sulphate is present, the amount will generally be at least 0.1% by weight. Similarly, if soap is present, the amount will generally be at least 0.1%. The weight ratio of alkane sulphonate to the total of alkyl ether sulphate and soap is preferably from 1:1 to 10:1 better 2:1 to 6:1.
  • R, R¹ and R² can, but do not need to be, the same, but preferably R¹ and R²CO₂ both have an average carbon chain length of 10 to 16 carbon atoms and may be predominantly of 12 carbon length.
  • The hypochlorite is desirably included in a quantity to provide from 0.1 to 8%, better 0.5 to 3% or 5% of available chlorine, by weight based on the whole composition. It is desirable to use hypochlorite in which the amount of available chlorine is at least twice the amount of any sodium chloride present. One supplier of suitable hypochlorite is Tahn and Mulhouse.
  • The composition will generally be alkaline. For this purpose alkali metal hydroxide may be included in a quantity between 0.1 and 1.5% by weight of the composition.
  • The amount of perfume dissolved in the composition, made soluble by the presence of alkyl ether sulphate and/or soap may lie in the range from 0.1 to 1.0% by weight of the composition. Preferably the amount of perfume is up to 0.6 or 0.7%.
  • A preferred composition according to this invention may have constituents and quantities as set out below.
    Figure imgb0004
  • Various other constituents are possible. Notable is 0.1 to 0.5% of alkali metal silicate. The pH of the composition is, suitably, greater than 11. This will give a lesser alkaline pH on dilution, especially when dilution is with hard tap water.
  • The invention is illustrated by the following Examples in which percentages are by weight based on the whole composition unless otherwise stated.
  • Example 1
  • A number of compositions were prepared using the following constituents:
       Secondary alkane sulphonate (SAS) with average 16-18 carbon atoms
       Linear alkyl ether sulphate (LES) in which the alkyl group has average 12-13 carbon atoms and the average degree of ethoxylation is 3
       Lauric soap
       Sodium hydroxide
       Perfume
  • A sodium hypochlorite solution which had the following characteristics as supplied:
  • Available chlorine
    over 315 g/litre
    NaOH
    10-20 g/litre
    Specific gravity
    1-315 to 1-320
    NaCl
    80 to 120 g/litre
  • The various compositions were made up in distilled water. All compositions contained sufficient hypochlorite to yield 1% available chlorine. It was noted whether the compositions were cloudy or clear. Compositions and results are set out in the following Tables 1 and 2:
    Figure imgb0005
    Figure imgb0006
  • Comparison of compositions 2, 3 and 4 show that increasing the amount of SAS from 2.0 to 2.8% was not sufficient to render the perfume soluble but addition of 0.26% soap did bring about solution of the perfume. Composition 12 shows that addition of 0.26% LES also brought about solution of the perfume. Compositions 5, 6 and 7 show the same effect at higher concentrations. Increasing the SAS level to 2.0 to 3.9% was not enough to bring about solution of 0.3% perfume but addition of 0.58% soap did cause the perfume to dissolve.
  • The solubility of perfume is low when sodium hydroxide has been added as shown by composition 1. Comparison of compositions 8 and 9 shows that increasing the level of SAS to 5% was not enough to bring about the solution of perfume. Comparison also with compositions 10 and 11 shows that addition of 0.5% LES or 0.5% soap did dissolve the perfume.
  • Example 2
  • A number of compositions were prepared using the same constituents as in Example 1, although in addition all compositions included 0.2% sodium silicate. Compositions and results are set out in the following Table 3.
    Figure imgb0007
  • Compositions 15, 16, 18 and 20 demonstrate that soap and LES can be used together to bring about the solubilisation of perfume.
  • Example 3
  • Compositions were prepared using the same materials as in Example 1, without sodium silicate, and with the amounts of the materials as set out in the following Table 4.
    Figure imgb0008
  • All of these compositions were clear solutions.
  • Example 4
  • Compositions were prepared in distilled water using the same materials as in Example 1 without sodium silicate, and with the amounts of the materials as set out in the following Table 5.
    Figure imgb0009
  • The compositions were used to remove various stains by a standard procedure. 1 ml of the composition was applied to a plastic tile bearing the stain. The tile was rubbed with the composition 200 times, using a machine to rub the tile. Each composition was used to clean three tiles bearing each stain. After the tiles had been cleaned in this way the effectiveness of cleaning was assessed by a panel of five evaluators whose assessments were averaged.
  • Composition D was found to be more effective than C on stains which were oil, two types of glue, vegetable fat and red pencil.
    Figure imgb0010
  • Example 5
  • The compositions of Example 2 were diluted with distilled water and used to wash a plastic tile. This was allowed to dry and the presence of streaks on the tile was assessed by the panel of evaluators. The amounts of composition diluted to one litre with water were 20, 25 and 50 grams. At each dilution composition D gave less streaking than composition C.

Claims (7)

  1. A perfumed aqueous liquid solution of alkali metal hypochlorite, also containing a surfactant mixture comprising
    (i) an alkane sulphonate of formula R-SO₃M in which R is an alkyl group with 8 to 22 carbon atoms and either
    (ii) an alkyl ether sulphate of formula R¹-(OC₂H₄)n SO₄M in which R¹ is an alkyl group with 8 to 20 carbon atoms and n has a value in the range from 0.5 to 12, and/or
    (iii) soap of formula R²CO₂M where R² is an alkyl or alkenyl group of 7 to 19 carbon atoms,
       each M denoting a solubilising cation;
       the amounts of the said surfactants, by weight based on the whole composition, being
    i) alkane sulphonate   1 to 10%
    ii) alkyl ether sulphate   0 to 3%
    iii) soap   0 to 3%
       but the total of (ii) and (iii) being 0.1 to 4%, the amount of amine oxide (if any) in the composition being less than half the content of other surfactants.
  2. A solution according to Claim 1 in which R¹ and R²CO₂- each have an average of 10 to 16 carbon atoms.
  3. A solution according to Claim 1 or Claim 2 wherein the content of sodium chloride is not more than half the amount of available chlorine by weight.
  4. A solution according to Claim 1 or Claim 2 containing, by weight based on the whole composition:
    i) alkane sulphonate   1 to 6%
    ii) alkyl ether sulphate   0 to 2%
    iii) soap   0 to 2%
    Total of (ii) and (iii)   0.2 to 3%.
  5. A solution according to Claim 4 wherein the content of sodium chloride is not more than half the amount of available chlorine by weight.
  6. A solution according to any one of Claims 1 to 5 containing 0.1 to 0.6% by weight perfume.
  7. A solution according to any one of the preceding claims wherein the content of hydrotrope is less than half the content of surfactant other than amine oxide (if any).
EP91302262A 1990-03-15 1991-03-15 Bleaching composition Expired - Lifetime EP0447261B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB909005873A GB9005873D0 (en) 1990-03-15 1990-03-15 Bleaching composition
GB9005873 1990-03-15

Publications (2)

Publication Number Publication Date
EP0447261A1 true EP0447261A1 (en) 1991-09-18
EP0447261B1 EP0447261B1 (en) 1995-01-25

Family

ID=10672693

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91302262A Expired - Lifetime EP0447261B1 (en) 1990-03-15 1991-03-15 Bleaching composition

Country Status (10)

Country Link
EP (1) EP0447261B1 (en)
JP (1) JPH0762154B2 (en)
AU (1) AU661269B2 (en)
BR (1) BR9106150A (en)
CA (1) CA2038189C (en)
DE (1) DE69106908T2 (en)
ES (1) ES2069200T3 (en)
GB (1) GB9005873D0 (en)
WO (1) WO1991013964A1 (en)
ZA (1) ZA911937B (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0478086A3 (en) * 1990-09-25 1993-06-16 Colgate-Palmolive Company Stable microemulsion disinfecting detergent composition
WO1994000549A1 (en) * 1992-06-26 1994-01-06 Unilever Plc Improvements to bleaching compositions
DE4333100C1 (en) * 1993-09-29 1994-10-06 Henkel Kgaa Bleaching and disinfecting compositions
WO1994024259A1 (en) * 1993-04-15 1994-10-27 Unilever Plc Hygienic cleaning composition and apparatus for spraying said composition
NL9401510A (en) * 1994-09-16 1996-05-01 Chem Y Surfactant composition, surfactant concentrate in liquid form, and aqueous bleaching agent having increased viscosity and cleaning activity
WO1999003960A2 (en) 1997-07-17 1999-01-28 Henkel Kommanditgesellschaft Auf Aktien Use of polyelectrolytes as sequestering agents
FR2773168A1 (en) * 1997-12-31 1999-07-02 Jeyes Group Plc LIQUID BLEACHING COMPOSITION
US6221827B1 (en) * 1998-12-17 2001-04-24 Henkel Kommanditgesellschaft Auf Aktien Viscoelastic bleaching and disinfecting compostions
WO2007025642A1 (en) * 2005-08-31 2007-03-08 Henkel Kommanditgesellschaft Auf Aktien Liquid hypohalite bleach
EP3078731A1 (en) * 2015-04-10 2016-10-12 Henkel AG & Co. KGaA Cleaning composition comprising bleach
US20220325205A1 (en) * 2018-01-16 2022-10-13 Tokuyama Corporation Treatment Liquid for Semiconductor Wafers, Which Contains Hypochlorite Ions
US12612580B2 (en) * 2018-01-16 2026-04-28 Tokuyama Corporation Treatment liquid for semiconductor wafers, which contains hypochlorite ions

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4131715A1 (en) * 1991-09-24 1993-03-25 Henkel Kgaa AQUEOUS CLEAR LIQUID CONCENTRATES OF ALKYL SULFATES
US8426349B2 (en) * 2009-05-26 2013-04-23 Delaval Holding Ab Chlorinated alkaline pipeline cleaner with methane sulfonic acid

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2094708A5 (en) * 1970-06-30 1972-02-04 Moreau Francis Foamed javel water-contg a detergent
FR2147081A1 (en) * 1971-07-23 1973-03-09 Basf Ag
EP0137551A1 (en) * 1983-09-23 1985-04-17 Unilever N.V. Liquid thickened bleaching composition
WO1986001823A1 (en) * 1984-09-21 1986-03-27 Lesieur-Cotelle Aqueous thickened cleaning compositions
EP0206534A1 (en) * 1985-05-30 1986-12-30 The Clorox Company Thickened aqueous cleanser
EP0304328A2 (en) * 1987-08-21 1989-02-22 Unilever Plc Machine dishwashing compositions
US4842757A (en) * 1988-01-21 1989-06-27 The Clorox Company Thickened liquid, improved stability abrasive cleanser

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ224700A (en) * 1987-05-26 1991-09-25 Bristol Myers Co Aqueous cleaner comprising alkali metal halogenite, perfume and an anionic surfactant stabiliser
CA2003857C (en) * 1988-12-15 1995-07-18 Lisa Michele Finley Stable thickened aqueous bleach compositions

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2094708A5 (en) * 1970-06-30 1972-02-04 Moreau Francis Foamed javel water-contg a detergent
FR2147081A1 (en) * 1971-07-23 1973-03-09 Basf Ag
EP0137551A1 (en) * 1983-09-23 1985-04-17 Unilever N.V. Liquid thickened bleaching composition
WO1986001823A1 (en) * 1984-09-21 1986-03-27 Lesieur-Cotelle Aqueous thickened cleaning compositions
EP0206534A1 (en) * 1985-05-30 1986-12-30 The Clorox Company Thickened aqueous cleanser
EP0304328A2 (en) * 1987-08-21 1989-02-22 Unilever Plc Machine dishwashing compositions
US4842757A (en) * 1988-01-21 1989-06-27 The Clorox Company Thickened liquid, improved stability abrasive cleanser

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0478086A3 (en) * 1990-09-25 1993-06-16 Colgate-Palmolive Company Stable microemulsion disinfecting detergent composition
GR1001316B (en) * 1990-09-25 1993-08-31 Colgate Palmolive Co Stable detergent disinfecting composition in a micro-emulsion
WO1994000549A1 (en) * 1992-06-26 1994-01-06 Unilever Plc Improvements to bleaching compositions
WO1994024259A1 (en) * 1993-04-15 1994-10-27 Unilever Plc Hygienic cleaning composition and apparatus for spraying said composition
DE4333100C1 (en) * 1993-09-29 1994-10-06 Henkel Kgaa Bleaching and disinfecting compositions
NL9401510A (en) * 1994-09-16 1996-05-01 Chem Y Surfactant composition, surfactant concentrate in liquid form, and aqueous bleaching agent having increased viscosity and cleaning activity
WO1999003960A2 (en) 1997-07-17 1999-01-28 Henkel Kommanditgesellschaft Auf Aktien Use of polyelectrolytes as sequestering agents
FR2773168A1 (en) * 1997-12-31 1999-07-02 Jeyes Group Plc LIQUID BLEACHING COMPOSITION
US6221827B1 (en) * 1998-12-17 2001-04-24 Henkel Kommanditgesellschaft Auf Aktien Viscoelastic bleaching and disinfecting compostions
WO2007025642A1 (en) * 2005-08-31 2007-03-08 Henkel Kommanditgesellschaft Auf Aktien Liquid hypohalite bleach
EP3078731A1 (en) * 2015-04-10 2016-10-12 Henkel AG & Co. KGaA Cleaning composition comprising bleach
WO2016162190A1 (en) * 2015-04-10 2016-10-13 Henkel Ag & Co. Kgaa Cleaning composition comprising bleach
US20220325205A1 (en) * 2018-01-16 2022-10-13 Tokuyama Corporation Treatment Liquid for Semiconductor Wafers, Which Contains Hypochlorite Ions
US12612580B2 (en) * 2018-01-16 2026-04-28 Tokuyama Corporation Treatment liquid for semiconductor wafers, which contains hypochlorite ions

Also Published As

Publication number Publication date
DE69106908T2 (en) 1995-07-13
JPH05505207A (en) 1993-08-05
ES2069200T3 (en) 1995-05-01
DE69106908D1 (en) 1995-03-09
BR9106150A (en) 1993-03-09
JPH0762154B2 (en) 1995-07-05
GB9005873D0 (en) 1990-05-09
ZA911937B (en) 1992-11-25
AU661269B2 (en) 1995-07-20
CA2038189A1 (en) 1991-09-16
EP0447261B1 (en) 1995-01-25
WO1991013964A1 (en) 1991-09-19
AU7448591A (en) 1991-10-10
CA2038189C (en) 1999-02-09

Similar Documents

Publication Publication Date Title
CA1189656A (en) Thickened alkali metal hypochlorite compositions
US4671895A (en) Liquid detergent compositions
EP0737242B1 (en) Thickened alkaly metal hypochlorite compositions
EP0667892B1 (en) Cleaning with short-chain surfactants
KR920006491A (en) Stable Microemulsion Detergent Compositions, Methods of Making the Same, and Methods for Cleaning and Sterilizing Stained Surfaces
AU661269B2 (en) Perfumed aqueous liquid bleaching composition
CA2191343C (en) Cleaning compositions thickened with n-alkyl-n-acyl amino acids and myristyl/cetyl dimethyl amine oxides
KR940010121B1 (en) Detergent composition
US4596672A (en) Detergent compositions
US4298492A (en) Built liquid detergent composition
EP0147943B1 (en) Bleaching compositions
US4288225A (en) Fluid, cold-stable, two-component washing compositions and method of washing textiles
EP0720642A1 (en) Thickneded aqueous detergent compositions with improved cleaning performance
US5403515A (en) Liquid cleaning compositions comprising primary alkyl sulphate and non-ionic surfactants
EP0971022B1 (en) Transparent liquid detergent containing alkylbenzenesulfonate anionic surfactant and sodium silicate
EP0110544A1 (en) Bleaching compositions
US5703036A (en) Thickened aqueous detergent compositions with improved cleaning performance
KR930003244B1 (en) Thickening Aqueous Composition
US5804545A (en) Stable alkaline chlorine compositions
US4986926A (en) Thickened alkali metal hypochlorite compositions
AU592843B2 (en) Thickened alkali metal hypochlorite compositions
US4286956A (en) Fluid, cold-stable, two-component washing compositions
RU2360955C2 (en) Hypochlorite bleaching composition
AU9411998A (en) Detergents, cleaning compositions and disinfectants comprising chlorine-active substances and fattyacid alkyl ester ethoxylates
WO1999031210A1 (en) Transparent liquid detergent containing sodium silicate

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): CH DE ES FR GB IT LI NL SE

17P Request for examination filed

Effective date: 19920220

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UNILEVER N.V.

Owner name: UNILEVER PLC

17Q First examination report despatched

Effective date: 19930810

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): CH DE ES FR GB IT LI NL SE

REF Corresponds to:

Ref document number: 69106908

Country of ref document: DE

Date of ref document: 19950309

ITF It: translation for a ep patent filed
ET Fr: translation filed
REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2069200

Country of ref document: ES

Kind code of ref document: T3

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

26 Opposition filed

Opponent name: JEYES GROUP LIMITED

Effective date: 19951024

NLR1 Nl: opposition has been filed with the epo

Opponent name: JEYES GROUP LIMITED

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLBO Opposition rejected

Free format text: ORIGINAL CODE: EPIDOS REJO

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19970228

Year of fee payment: 7

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 19970130

NLR2 Nl: decision of opposition
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980331

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980331

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20000214

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20000221

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20000225

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20000228

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20000314

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20000320

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20010315

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20010316

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20010316

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20011001

EUG Se: european patent has lapsed

Ref document number: 91302262.0

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20010315

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20011130

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20011001

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020101

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20030303

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20050315