WO1998046718A1 - Hypochlorite bleaching compositions and delivery systems therefor - Google Patents

Hypochlorite bleaching compositions and delivery systems therefor Download PDF

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Publication number
WO1998046718A1
WO1998046718A1 PCT/EP1998/001897 EP9801897W WO9846718A1 WO 1998046718 A1 WO1998046718 A1 WO 1998046718A1 EP 9801897 W EP9801897 W EP 9801897W WO 9846718 A1 WO9846718 A1 WO 9846718A1
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WO
WIPO (PCT)
Prior art keywords
hypochlorite
oxygen transfer
transfer agent
bleaching
bleaching composition
Prior art date
Application number
PCT/EP1998/001897
Other languages
English (en)
French (fr)
Inventor
Jayne Elisabeth Nation
Katherine Mary Thompson
David William Thornthwaite
Original Assignee
Unilever Plc
Unilever N.V.
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
Application filed by Unilever Plc, Unilever N.V. filed Critical Unilever Plc
Priority to JP54342098A priority Critical patent/JP4302191B2/ja
Priority to EP98922632A priority patent/EP0975730B1/en
Priority to CA002286731A priority patent/CA2286731C/en
Priority to PL336264A priority patent/PL192418B1/pl
Priority to HU0001681A priority patent/HUP0001681A3/hu
Priority to AU75214/98A priority patent/AU734077B2/en
Priority to BR9808568-9A priority patent/BR9808568A/pt
Priority to DE69808069T priority patent/DE69808069T2/de
Publication of WO1998046718A1 publication Critical patent/WO1998046718A1/en

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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
    • C11D3/395—Bleaching agents
    • 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
    • C11D3/26—Organic compounds containing nitrogen
    • 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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • 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
    • C11D3/26—Organic compounds containing nitrogen
    • C11D3/28—Heterocyclic compounds containing nitrogen in the ring
    • 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
    • C11D3/395—Bleaching agents
    • C11D3/3951—Bleaching agents combined with specific additives
    • 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
    • C11D3/395—Bleaching agents
    • C11D3/3956—Liquid compositions

Definitions

  • the present invention relates to hypochlorite bleaching compositions.
  • hypochlorite is a powerful oxidising agent, which can decolourise a very large number of coloured compounds found in soils but which has significant limitations when used to bleach certain fatty and pyrolised soils. There is a need to provide bleaching compositions which can attack these soils. There is also a need to reduce the usage of hypochlorite.
  • oxygen transfer agents such as ' imine quat ' compounds to promote the bleaching activity of peroxygen compounds.
  • an oxygen transfer agent is a species which reacts with a peroxygen compound such as hydrogen peroxide to form an oxidative bleaching species which oxidative bleaching species, subsequently reacts with a substrate to regenerate the oxygen transfer agent.
  • oxygen transfer agents include N-methyl- 3.4-dihydroisoquinolinium salts.
  • US 5360569 discloses that imine quat molecules can be used to promote the activity of TAED/perborate bleaching compositions. These systems are believed to work by generating per-acetic acid in situ. This organic peroxide is believed to interact with the i ine quat. to bring about the bleaching activity.
  • US 5360568 discloses that imine quat molecules can be used to promote the activity of monopersulphate (an inorganic peroxygen compound) and peroxy-adipyl-phthalimide (PAP) (an the organic peracid) .
  • monopersulphate an inorganic peroxygen compound
  • PAP peroxy-adipyl-phthalimide
  • imine quat compounds can significantly boost the bleaching effect of hypochlorite.
  • the present invention provides a bleaching composition of pH 8-14 which comprises an oxygen transfer agent and hypochlorite or a source thereof.
  • a further aspect of the present invention provides a method for bleaching a stained substrate which comprises the step of treating the substrate with a bleaching composition of pH 8-14 which bleaching composition comprises an oxygen transfer agent and hypochlorite or a source thereof.
  • a further aspect of the present invention comprises a delivery- system comprising a first reservoir for liquid and a second reservoir for liquid, and means to dispense at least a part of the content of each said reservoir to a common point, wherein the first said reservoir for liquid contains a hypochlorite or source thereof and the second said reservoir for liquid contains an oxygen transfer agent.
  • hypochlorite or at least a source of it, which may preferably be in the form of a so-called chlorine release agent is an essential component of the compositions according to the present invention.
  • hypochlorite is a reactive species, this will place some limitations on the other components which can be present. These are described in greater detail below.
  • Hypochlorite is preferably present at a level of 0.1-10%wt on product, more preferably l-5%wt on product.
  • the weight ratio of the hypochlorite to the oxygen transfer agent falls in the range 5:1 to 20:1.
  • Suitable water-soluble, chlorine release agents useful in accordance with the invention include chlorinated cyanurates, phthalimides, p-toluene sulphonamides, azodicarbonamides, hydantoins, glycoluracils, amines and melamines.
  • a particularly preferred chlorine release agent for use in toilet blocks is sodium dichlorocyanurate (NaDCCA) .
  • NaDCCA sodium dichlorocyanurate
  • the chlorine release agent is typically present in an amount of 10-30% and most preferably at around 25%.
  • Oxidan DCN/WSG (TM) ex Sigma is envisaged as a suitable bleaching agent .
  • Oxygen transfer agents for use in the present invention include, but are not limited to, the imine quat. N-methyl-3.4- dihydroisoquinolinium salts. Where these salts are used, suitable counter-ions include halides, sulphate, methosulphate, sulphonate, p-toluene sulphonate and phosphate. Oxygen transfer agents which comprise a quaternary nitrogen atom are preferred. In the alternative, the oxygen transfer agent can be a sulphonimine .
  • R x and R 4 are in a cis- relation and are substituted or unsubstituted moieties selected from the group consisting of hydrogen, phenyl, aryl, heterocyclic ring, alkyl and cycloalkyl radicles:
  • R 2 is a substituted or unsubstituted moiety selected from the group consisting of hydrogen, phenyl, aryl, heterocyclic ring, alkyl, cycloalkyl, nitro, halo, cyano, alkoxy, keto, carboxylic acid and carboalkoxy groups:
  • R 3 is a substituted or unsubstituted moiety selected from the group consisting of hydrogen, phenyl, aryl, heterocyclic ring, alkyl, cycloalkyl, nitro, halo and cyano groups:
  • R x with R 2 and R 3 respectively together form a moiety selected from the group consisting of cycloalkyl, polycyclo, heterocyclic and aromatic ring systems.
  • Heterocyclic rings include cycloaliphatic and cycloaromatic type radicals incorporating an oxygen, sulphur and/or nitrogen atom within the ring system.
  • Representative nitrogen heterocycles include pyridine, pyrrole, imidazole, triazole, tetrazole, morpholine, pyrrolidone, piperidene and piperazine.
  • Suitable oxygen heterocycles include furan, tetrahydrofuran and dioxane.
  • Sulphur heterocycles may include thiophene and tetrahydrothiophene .
  • R 1# R 2 , R 3 and R 4 includes a substituent which is nitro, ⁇ halo, cyano, C1-C20 alkyl, amino, aminoalkyl, thioalkyl, sulphoalkyl, carboxyester, hydroxy, C1-C20 alkoxy, polyalkoxy, or C1-C40 quaternary di- or tri-alkyl ammonium.
  • Preferred oxygen transfer agents are quaternary imine salts, particularly those set forth in US patent specification 5,360,568 (Madison and Coope) , more particularly the substituted or unsubstituted isoquinolinium salts, preferably the 3,4 di-hydro isoquinolinium salts and more preferably the N-methyl 3,4 di-hydro-isoquinolinium salts.
  • N-methyl-3, 4- dihydro-6 , 7-dimethoxyisoquinolinium tosylate gives a performance benefit over that observed for hypochlorite.
  • N-methyl 3,4 di-hydro-isoquinolinium p-toluene sulphonate is a particularly preferred oxygen transfer agent.
  • the oxygen transfer agents are present of levels of 0.001-10%wt on product.
  • the oxygen transfer agents are present at levels of 0.01-l%wt on product, more preferably 0.1-0.5%wt on product.
  • compositions according to the invention further comprise one or more surfactant species.
  • surfactants can be nonionic, anionic, cationic, amphoteric or zwitterionic provided that they, and where appropriate their counter-ions, do not react substantially with the oxygen transfer agent or the hypochlorite.
  • Suitable nonionic detergent active compounds are alkoxylated alkanols. These can be broadly described as compounds produced by the condensation of alkylene oxide groups, which are hydrophilic in nature, with an organic hydrophobic compound which may be aliphatic or alkyl aromatic in nature. The length of the hydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
  • Particular examples include the condensation product of aliphatic alcohols having from 8 to 22 carbon atoms in either straight or branched chain configuration with ethylene oxide, such as a coconut oil ethylene oxide condensate having from 3 to 10 moles of ethylene oxide per mole of coconut alcohol; condensates of alkylphenols whose alkyl group contains from 6 to 12 carbon atoms with 3 to 10 moles of ethylene oxide per mole of alkylphenol .
  • the preferred alkoxylated alcohol nonionic surfactants are ethoxylated alcohols having a chain length of C9-C11 and an EO value of at least 3 but less than 10.
  • Particularly preferred nonionic surfactants include the condensation products of C 10 alcohols with 3-8 moles of ethylene oxide.
  • the preferred ethoxylated alcohols have a calculated HLB of 10-16.
  • An example of a suitable surfactant is ' IMBENTIN 91-35 OFA' (TM, ex. Kolb AG) a C 9 . u alcohol with five moles of ethoxylation.
  • Alternative surfactants include a ine oxides, amines and/or ethoxylates thereof. Amine oxides with a carbon chain length of C8-C14 are particularly preferred.
  • Combinations of surfactants can be chosen to give appropriate thickening of the composition.
  • Combinations of amine oxides and anionic surfactants, including fatty acids (soaps) and anionic hydrotropes, are known to thicken.
  • the amount of nonionic detergent active to be employed in the composition of the invention will generally be from 0.01 to 30%wt, preferably from 0.1 to 20%wt, and most preferably from 3 to 10%wt for non-concentrated products. Concentrated products will have 10-20%wt nonionic surfactant present, whereas dilute products suitable for spraying will have 0.1-5%wt nonionic surfactant present.
  • pH of compositions according to the present invention falls in the range 8-14. pH of compositions is preferably 9-12, more preferably 10-11. At these higher pH's we have found that the composition penetrates more readily into the soils.
  • compositions according to the present invention include those typically present in bleaching and/or cleaning compositions.
  • compositions which contain hypochlorite it is useful to include a metal ion complexing agent to retard decomposition of the hypochlorite by any metal ions which may be present as contaminants or such as are introduced during processing. Again, these components should be selected such that they do not react do not react substantially with the oxygen transfer agent or the hypochlorite.
  • cleaning and/or disinfecting compositions according to the invention will further comprise at least 1% of a solvent of the form R ⁇ O- (EO) m - (PO) n -R 2 , wherein R x and R 2 are independently C2-6 alkyl or H, but not both hydrogen, m and n are independently 0-5.
  • the solvent is selected from the group comprising di-ethylene glycol mono n- butyl ether, mono-ethylene glycol mono n-butyl ether, propylene glycol n-butyl ether, isopropanol, ethanol, butanol and mixtures thereof.
  • the level of solvent in cleaning and disinfecting compositions is 1-10%, with a solvent: nonionic ratio of 1:3-3:1 being particularly preferred.
  • compositions according to the present invention are liquids, they can be water-thin or thickened. Thickened compositions are advantageous in that they cling to sloping surfaces and find particular utility in toilet cleaners.
  • Suitable thickening agents include amine oxide and soap as mentioned above and systems based on nonionic surfactants.
  • compositions according to the invention can also contain, in addition to the ingredients already mentioned, various other optional ingredients such as, colourants, optical brighteners, soil suspending agents, gel-control agents, freeze-thaw stabilisers, perfumes and opacifiers.
  • various other optional ingredients such as, colourants, optical brighteners, soil suspending agents, gel-control agents, freeze-thaw stabilisers, perfumes and opacifiers.
  • a particularly preferred compositions according to the present invention comprises a bleaching composition having a pH of 9- 12, said composition being an aqueous liquid and comprising:
  • hypochlorite at a level of 0.1-10%wt on product
  • Products according to the present invention are generally liquids and preferably aqueous. However, other product forms including pastes and solids are also envisaged. As will be appreciated, the product form is largely determined by the end use and consequently liquids are generally suitable for use as hard surface cleaners, including cleaners for industrial, institutional and domestic cleaning and/or disinfection of hard surfaces including metal, plastics materials or other polymers, ceramic, and glass surfaces.
  • the method of the present invention can be applied in the cleaning of surfaces used for the preparation of food and beverages (e.g. worktops, conveyor systems and utensils) or other industrial, institutional and domestic surfaces such as sanitary ware, industrial, institutional and domestic fluid supply applications, for disinfection of medical, surgical or dental apparatus, equipment, facilities or supplies, catheters, contact lens', surgical dressings or surgical instruments, in horticultural applications, e.g. for sterilising the surfaces of greenhouses, for soft surfaces including fabrics (including in dressings, wipes and cloths), and non-living materials of biological origin (such as wood) .
  • Solid product forms are suitable for use as toilet and urinal, rim or cistern blocks and other uses where slow or delayed release of the components is required.
  • a further aspect of the present invention comprises a delivery system comprising a first reservoir for liquid and a second reservoir for liquid, and means to dispense at least a part of the content of each said reservoir to a common point, wherein the first said reservoir for liquid contains a hypochlorite or source thereof and the second said reservoir for liquid contains an oxygen transfer agent.
  • the oxygen transfer agent is iiranine quat as hypochlorite and imine quat are not mutually stable and for long term storage. Consequently it is advantageous that the materials are delivered from a dual-compartment system with mixing occurring as, or shortly before, the product is applied to the surface. Mixing of the components produces a composition according to invention as described above.
  • a sodium hypochlorite/Imine Quat system may be delivered from such a dual-compartment spray pack, by separating the components as follows :
  • Solution A sodium hypochlorite (2% w/w) , pH adjusted to 11.0.
  • Solution B Imine Quat (2% w/w) , pH adjusted to a figure in the range 5.0 - 6.0.
  • Solutions (A & B) are stable for > 2 weeks and when dispensed from a suitable pack in equal proportions produce a hypochlorite/Imine Quat solution with a pH of 10.5.
  • the bleaching efficacy of this solution when appraised against the curcumin/oil model soil, is equal to that produced from a freshly prepared 'one-pot' reaction mixture.
  • the precise levels of alkali necessary to achieve the final desired pH on mixing will vary depending on the initial alkalinity of the sodium hypochlorite solution. It is preferred that suitable levels of surfactants, perfume etc are added to solutions of type B, but not to solutions of type A. The levels of these components will vary, depending on the mixing ratio of the solutions, so as to achieve the preferred levels of components in the final product as described above.
  • the curcumin/oil stain is prepared by mixing 19 g of vegetable oil and 180 g of ethanol and then adding 1 g of pure curcumin (a pigment found in curry powder) . After thorough stirring, the resulting solution is sprayed onto the tiles using two different methods to give two different soiling characteristics.
  • a first method used a spray gun driven by an airbrush propellent canister so as to give a uniform surface coverage.
  • a second method used a compressor driven spray gun to give a higher soil loading that in the first method.
  • the oxygen transfer agent was N- ethyl 3,4 di-hydro isoquinolinium p-toluene sulphonate.
  • the preparation of this material is described in US 5360569 and US 5360568 which are incorporated herein by reference. The material is referred to below as the ' imine quat ' .
  • Examples were performed at room temperature.
  • a glass ring of diameter 50 mm and height 15 mm, is placed over the centre of the stained tile and 5 cm 3 of the aqueous bleach or surfactant solution is pipetted within the annulus of the ring.
  • the solution is allowed to remain in contact with the stained tile surface for 30 seconds, after which the glass ring is removed and the solution poured away.
  • the tile is immediately rinsed with demineralised water for a further 30 seconds and then allowed to dry. Each solution is used to treat two tiles.
  • the extent of stain removal is assessed visually by a panel of at least 15 people, using a standard scale. Tiles are graded on an integer scale ranging from 0 to 5, where 0 denotes no visible soil removal and 5 corresponds to total removal. A minimum of two stained tiles are treated with each bleach solution and mean scores for each system are calculated by averaging the scores from both tiles.
  • the method of soil preparation is as described before, except that the soil is sprayed onto the Decamel surface using a air compressor. Systems are scored for soil removal as described previously.
  • sodium hypochlorite and Imine Quat are not mutually stable for long term storage it is preferable that they are delivered from a dual-compartment system with mixing occurring as the product is applied to the surface.
  • the sodium hypochlorite (1% w/w) /Imine Quat (1% w/w) system were delivered from a dual-compartment spray pack, by separating the components as follows:
  • Solution A sodium hypochlorite (2% w/w) , pH adjusted to 11.0.
  • Solution B Imine Quat (2% w/w) , pH adjusted to a figure in the range 5.0 - 6.0. Solutions (A & B) were found to be stable for > 2 weeks and when dispensed from a suitable pack produce a hypochlorite/Imine Quat solution with a pH of 10.5. The bleaching efficacy of this solution, when appraised against the curcu in/oil model soil, is equal to that produced from a freshly prepared 'one-pot' reaction mixture.

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  • 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)
  • Treatment Of Water By Oxidation Or Reduction (AREA)
PCT/EP1998/001897 1997-04-16 1998-03-23 Hypochlorite bleaching compositions and delivery systems therefor WO1998046718A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP54342098A JP4302191B2 (ja) 1997-04-16 1998-03-23 次亜塩素酸塩漂白組成物およびその送出システム
EP98922632A EP0975730B1 (en) 1997-04-16 1998-03-23 Hypochlorite bleaching compositions and delivery systems therefor
CA002286731A CA2286731C (en) 1997-04-16 1998-03-23 Hypochlorite bleaching compositions and delivery systems therefor
PL336264A PL192418B1 (pl) 1997-04-16 1998-03-23 Kompozycja bieląca
HU0001681A HUP0001681A3 (en) 1997-04-16 1998-03-23 Hypochlorite bleaching composition, method for bleaching and delivery systems therefor
AU75214/98A AU734077B2 (en) 1997-04-16 1998-03-23 Hypochlorite bleaching compositions and delivery systems therefor
BR9808568-9A BR9808568A (pt) 1997-04-16 1998-03-23 Composição alvejante, processo para alvejar um substrato manchado, e, sistema de distribuição.
DE69808069T DE69808069T2 (de) 1997-04-16 1998-03-23 Hypochlorithaltige bleichmittelzusammensetzungen und freisetzungssysteme dafür

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9707719.2A GB9707719D0 (en) 1997-04-16 1997-04-16 Improvements relating to bleaching compositions comprising hypochlorite
GB9707719.2 1997-04-16

Publications (1)

Publication Number Publication Date
WO1998046718A1 true WO1998046718A1 (en) 1998-10-22

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PCT/EP1998/001897 WO1998046718A1 (en) 1997-04-16 1998-03-23 Hypochlorite bleaching compositions and delivery systems therefor

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US (1) US6042744A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
EP (1) EP0975730B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
JP (1) JP4302191B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
KR (1) KR20010006407A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
CN (1) CN1252834A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
AR (1) AR012406A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
AU (1) AU734077B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
BR (1) BR9808568A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
CA (1) CA2286731C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
DE (1) DE69808069T2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
ES (1) ES2183363T3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
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HU (1) HUP0001681A3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
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PL (1) PL192418B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html)
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US6165448A (en) * 1998-09-25 2000-12-26 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Oral composition with an improved teeth whitening effect
DE102007047688A1 (de) 2007-10-04 2009-04-09 Henkel Ag & Co. Kgaa Aufhellmittel mit kationischen 3,4-Dihydroisochinoliniumderivaten und Wasserstoffperoxid
WO2018103973A1 (en) * 2016-12-09 2018-06-14 Unilever N.V. Sanitising system

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BR9803631A (pt) * 1998-05-27 2000-02-22 Lazaro Sebastiao Roberto Processo de preparação de agente biocatalisante; agente biocatalisante assim obtido; processo para preparação de fertilizante ornanomineral a partir de uma ampla série de resìduos orgânicos; fertilizante organomineral obtido; composição fertilizante organomineral; processo de aplicação da ciomposição fertilizante organomineral a saber do fertilizante organomineral na agricultura.
US20050282722A1 (en) * 2004-06-16 2005-12-22 Mcreynolds Kent B Two part cleaning composition
EP1811014B1 (en) 2006-01-23 2010-04-21 The Procter and Gamble Company A composition comprising a pre-formed peroxyacid and a bleach catalyst
CA2635927A1 (en) * 2006-01-23 2007-08-02 The Procter And Gamble Company A composition comprising a lipase and a bleach catalyst
EP1979457A2 (en) 2006-01-23 2008-10-15 The Procter and Gamble Company A composition comprising a lipase and a bleach catalyst
EP2038395B1 (en) 2006-07-07 2013-01-02 The Procter & Gamble Company A composition comprising a cellulase and a bleach catalyst
CN106426667B (zh) * 2016-11-18 2018-11-09 青岛双星橡塑机械有限公司 自动换模装置
KR101877168B1 (ko) * 2017-03-28 2018-07-10 김현서 부착형 오염물 제거제

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ES2183363T3 (es) 2003-03-16
IN190055B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) 2003-06-07
KR20010006407A (ko) 2001-01-26
CN1252834A (zh) 2000-05-10
MY120735A (en) 2005-11-30
CA2286731C (en) 2007-09-11
HUP0001681A2 (hu) 2000-09-28
HUP0001681A3 (en) 2003-02-28
EP0975730A1 (en) 2000-02-02
EP0975730B1 (en) 2002-09-18
PL336264A1 (en) 2000-06-19
AU734077B2 (en) 2001-05-31
PL192418B1 (pl) 2006-10-31
ZA982061B (en) 1999-09-13
DE69808069T2 (de) 2003-06-05
JP2001519848A (ja) 2001-10-23
AR012406A1 (es) 2000-10-18
GB9707719D0 (en) 1997-06-04
JP4302191B2 (ja) 2009-07-22
TR199902395T2 (xx) 2000-05-22
US6042744A (en) 2000-03-28
DE69808069D1 (de) 2002-10-24
AU7521498A (en) 1998-11-11
CA2286731A1 (en) 1998-10-22

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