EP0437988A2 - Waschmittelzusatz auf der Basis eines Polyphosphats und eines optisch aktiven Mittels, Verfahren zu dessen Herstellung und seine Verwendung als Waschmittel - Google Patents

Waschmittelzusatz auf der Basis eines Polyphosphats und eines optisch aktiven Mittels, Verfahren zu dessen Herstellung und seine Verwendung als Waschmittel Download PDF

Info

Publication number
EP0437988A2
EP0437988A2 EP90403320A EP90403320A EP0437988A2 EP 0437988 A2 EP0437988 A2 EP 0437988A2 EP 90403320 A EP90403320 A EP 90403320A EP 90403320 A EP90403320 A EP 90403320A EP 0437988 A2 EP0437988 A2 EP 0437988A2
Authority
EP
European Patent Office
Prior art keywords
polyphosphate
compound according
detergent
substance
detergent compound
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
EP90403320A
Other languages
English (en)
French (fr)
Other versions
EP0437988B1 (de
EP0437988A3 (en
Inventor
Daniel Joubert
Jean Csomo
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.)
Rhodia Chimie SAS
Original Assignee
Rhone Poulenc Chimie SA
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 Rhone Poulenc Chimie SA filed Critical Rhone Poulenc Chimie SA
Publication of EP0437988A2 publication Critical patent/EP0437988A2/de
Publication of EP0437988A3 publication Critical patent/EP0437988A3/fr
Application granted granted Critical
Publication of EP0437988B1 publication Critical patent/EP0437988B1/de
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
    • C11D3/16Organic compounds
    • C11D3/162Organic compounds containing Si
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0034Fixed on a solid conventional detergent ingredient
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0063Photo- activating compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
    • 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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • C11D3/42Brightening agents ; Blueing agents

Definitions

  • the present invention relates to a detergent compound based on polyphosphate, of a product chosen from the group comprising siliconates, siliconate derivatives and silicone resins and of a substance intended to be distributed uniformly over a washing room as well as its preparation. It also relates to the detergent use of this compound.
  • Detergent compositions in the form of powder in particular contain in addition to their usual constituents of the builders or surfactants type, many additives such as dyes, optical brighteners, photobleaching agents, softening agents, antiseptic agents, etc.
  • the main object of the invention is therefore a means or a system making possible the homogeneous distribution of a detergent additive on the article to be washed, this whatever the type of washing used.
  • a second object of the invention is the preparation of such a system.
  • the detergent compound according to the invention is characterized in that it comprises an at least partially hydrated polyphosphate, this polyphosphate incorporating or supporting at least one substance intended to be distributed uniformly over the part to be washed and a product chosen from the group comprising siliconates, siliconate derivatives and silicone resins.
  • the process for preparing the detergent compound consists in mixing with the anhydrous or partially hydrated polyphosphate an aqueous solution comprising the substance and the aforementioned product.
  • the invention relates to a detergent composition which is characterized in that it comprises a detergent compound of the above type or prepared by the process described above.
  • the detergent compound defined above ensures a delayed release of the additive, and thus makes it possible to reduce the risks of additive - laundry contact. It therefore provides a completely homogeneous distribution of this additive on the laundry and this even for hand washing in a bowl. In addition, this presentation of the additive makes it possible to impart a visual effect to the washing powder if necessary.
  • the detergent compound according to the invention therefore consists of three types of elements, namely an at least partially hydrated polyphosphate incorporating or supporting on the one hand, at least one substance intended to be uniformly distributed over a part to be washed (called in the rest of the description "the substance”), and on the other hand a product chosen from siliconates, siliconate derivatives and silicone resins, (called in the rest of the description "the product”).
  • the detergent compound has the following particular structure:
  • the aforementioned substance is located at least partly inside or at the heart of the polyphosphate-based support grain.
  • the aforementioned product is located at least partially on the surface of said support or is adsorbed thereon.
  • the optimum embodiment is that for which all of the above substance is placed inside the polyphosphate grain and all of the above product on the surface thereof or adsorbed thereon.
  • any intermediate configuration can be envisaged without departing from the scope of the present invention, in which a part of the substance would be present on the surface of the polyphosphate and a part of the product would be located inside of it.
  • the support based on polyphosphate can be composed of pyrophosphate or tripolyphosphate.
  • TPP tripolyphosphate
  • polyphosphate of the compound according to the invention is at least partially hydrated, that is to say that it has a hydration rate of at least 8% by weight.
  • this hydration rate is at least 10%, preferably at least 15% and in particular between 15 and 18%.
  • This hydration results from the process for preparing the compound. As will be described later, it is this water of hydration which makes it possible to introduce the substance into the heart of the support.
  • the support must have a density of between 0.4 and 0.8 and preferably between 0.6 and 0.8.
  • polyphosphate and in particular TPP in the form of particles, very difficultly absorbs water, which consequently hinders the introduction via water, substance at the heart of the particles, and that in sufficient quantity.
  • the density of the support is less than 0.4, the compound is difficult to handle.
  • particles are generally used whose average size is between 200 ⁇ m and 800 ⁇ m, and preferably between 600 ⁇ m and 700 ⁇ m. This particle size is recommended to obtain the optical effect described above, when the aforementioned substance is colored.
  • TPP support Another preferred characteristic of the invention in the case of a TPP support is that it is in the form of phase 1.
  • an alkaline polyphosphate More particularly, the sodium TPP is retained as a support according to the invention.
  • the polyphosphate content is between 78 and 91.8% by weight, expressed as anhydrous polyphosphate and relative to the total weight of the detergent compound.
  • Another constituent of the detergent compound according to the present invention is the substance intended to be distributed uniformly over a room to be washed. It is understood that the compound of the invention can comprise several substances of this type at the same time. Said substance can in particular be an optically active agent. This agent can be chosen from the group of optical brighteners, photobleaching agents, and dyes.
  • compositions of stilbene, triazole and benzidine-sulfone in particular sulfonated substituted triazinyl-stilbene, naphthotriazole- sulfonated stilbene, benzidine-sulfone, etc., the most preferred being combinations of stilbene and triazole.
  • porphine derivatives As photobleaching agents, mention may be made, inter alia, of porphine derivatives, but also the compounds described in French patent application FR-A- 2,564,481 in the name of RHONE-POULENC CHEMISTRY, the teaching of which is incorporated here in the present description and corresponding to the water-soluble salts or disels of the acid corresponding to the following general formula (1): and whose hydrogen atoms carried by the carbons marked 1 to 8 can be substituted in particular by atoms of Cl, Br and I.
  • eosin "Yellow” but also 1,2-dibromo fluorescein, that is to say the dibromo salt or disel of formula (1), dibromo-3, 4 fluorescein, phloxin i.e. 1,2,3,4 tetrabromo-5,6,7,8 fluorescein, 1,2-diodo fluorescein, 3,4-diodo fluorescein and tétraiodo-1,2,3,4 tétrachloro-5,6,7,8 fluoresceine or "Rose Bengal”.
  • 1,2-dibromo fluorescein that is to say the dibromo salt or disel of formula (1), dibromo-3, 4 fluorescein, phloxin i.e. 1,2,3,4 tetrabromo-5,6,7,8 fluorescein, 1,2-diodo fluorescein, 3,4-diodo fluorescein and tétraiodo
  • E 100 curcumin
  • E 102 thyroidrazine
  • E 120 cochineal
  • E 123 asmaranth
  • E 127 erythrosine
  • E 131 patternent blue
  • E 132 indigotine
  • E 140 chlororophylls
  • a substance according to the invention belonging to the group of photobleaching agents, it is possible to choose a derivative of tetrabenzo-tetraazoporphine.
  • TINOLUX BBS As a derivative of this type which can also be used in the context of the invention, mention may be made of TINOLUX BBS from the company CIBA-GEIGY.
  • the content of substance intended to be distributed uniformly of the aforementioned type for example is generally 0.1 to 2% by weight relative to the total weight of the detergent compound.
  • the detergent compound comprises a product chosen from siliconates, siliconate derivatives and silicone resins.
  • Siliconates are well known products, they are salts of siliconic acid or its derivatives.
  • R is a hydrocarbon residue generally of 1 to 18 carbon atoms, optionally substituted by a halogen atom, an amino group, ether, ester, epoxy, mercapto, cyano, (poly) glycol;
  • n is an integer or fractional number varying between 0.1 and 3;
  • M is an alkali metal or an ammonium or phosphonium group.
  • R is a hydrocarbon residue of 1 to 10 carbon atoms and more particularly of 1 to 6 atoms.
  • R can be an alkyl radical, for example methyl, ethyl, propyl, butyl, isobutyl; an alkenyl radical such as for example vinyl, an aryl radical, for example phenyl or naphthyl, an arylalkyl radical such as for example benzyl or phenyl-ethyl, alkylaryl such as for example tolyl, xylyl, or an araryl radical such as biphenylyl.
  • alkyl radical for example methyl, ethyl, propyl, butyl, isobutyl
  • an alkenyl radical such as for example vinyl
  • an aryl radical for example phenyl or naphthyl
  • an arylalkyl radical such as for example benzyl or phenyl-ethyl
  • alkylaryl such as for example tolyl, xylyl, or an araryl radical such as biphenylyl.
  • M there may be mentioned more particularly sodium or potassium as well as the groups N+R'4, P+R'4 in which R 'are identical or different and are hydrocarbon residues of 1 to 6 carbon atoms.
  • alkaline siliconates are used.
  • Alkaline earth siliconates can also be used.
  • alkylsiliconates and in particular alkaline alkylsiliconates such as, for example, sodium or potassium methylsiliconates.
  • alkali or alkaline earth siliconates are products, most of which are commercially available.
  • silanes having 3 hydrolyzable groups such as halogen atoms, alkoxy radicals, followed by dissolution of the product obtained in a solution of a strong inorganic base in proportions such as there is at least one equivalent in base per atom of silicon (see for example US-A-2,441,422, US-A-2,441,423).
  • hydrophobing agent can also be chosen from siliconate derivatives.
  • derivative products is meant here the condensation products of the products corresponding in particular to formula (2) described above, or those resulting from the at least partial polymerization into silicone compounds or polymers.
  • a third type of supported products which can be used in the context of the present invention is that of silicone resins.
  • silicone resins are well-known branched organopolysiloxane polymers which are commercially available. They have, per molecule, at least two different units chosen from those of formula R3SiO0 , 5 (unit M), R2SiO (unit D), RSiO1 , 5 (unit T) and SiO2 (unit Q).
  • radicals R are identical or different and are chosen from linear or branched alkyl radicals, vinyl, phenyl, trifluoro-3,3,3 propyl radicals.
  • the alkyl radicals have 1 to 6 carbon atoms inclusive.
  • alkyl radicals R of methyl, ethyl, isopropyl, tert-butyl and n-hexyl radicals.
  • These resins are preferably hydroxylated and in this case have a weight content of hydroxyl group of between 0.1 and 10%.
  • resins examples include MQ resins, MDQ resins, TD resins and MDT resins.
  • Resins having a molecular mass of less than 25,000 can be used more particularly.
  • the content of supported product and in particular of siliconate is generally from 0.1 to 2% by weight relative to the total weight of the detergent compound.
  • the polyphosphate, and in particular the TPP, anhydrous or partially hydrated can be mixed in a single step with the aforementioned substance and product, at least one of these being provided in the form of an aqueous solution.
  • Another variant of the process according to the invention consists in preparing the detergent compound in two mainly stages.
  • the polyphosphate and in particular the TPP, anhydrous or partially hydrated, is mixed with the aforementioned substance and water is brought to this mixture for the hydration of the polyphosphate. You can do it by different methods.
  • the polyphosphate, the water and the substance are mixed at the same time.
  • the substance can be brought in the form of an aqueous solution and it is this solution which at least partially provides the necessary water.
  • the water brought in at this stage penetrates into the polyphosphate grain and at the same time allows the introduction of the substance inside the grain itself.
  • the second step consists in adding the above-mentioned product to the mixture obtained previously.
  • the amount of water used in the first step represents at least 50% of the water used entirely in the process for the desired hydration rate of the polyphosphate.
  • a maturing of each of the resulting mixtures is carried out.
  • Such an operation ensures better diffusion of the water and of the constituents of the compound and promotes the crystallization of the water in the TPP particles thus treated.
  • Ripening allows each mixture to cool because the hydration of TPP is an exothermic reaction. It is carried out by stirring each mixture obtained for a period of approximately 20 minutes in an atmosphere having a non-saturated vapor pressure.
  • the detergent compound according to the invention finds its application as a constituent in any detergent application, in particular compositions of the powder type.
  • these compositions can comprise a builder of the phosphate, polyphosphate, zeolite, silicate or carbonate type. They can also include surfactants, anionic, nonionic, cationic, amphoteric. They can also include bleaching agents of the perborate type, foam control agents, anti-deposition agents, fluorescent agents and all additives of the perfume, enzymes, sequestering, soluble polymers, dyes type for example.
  • the content of detergent compound in a detergent composition is generally between 1 and 10% by weight.
  • the mixing of the constituent elements of the compound was carried out thanks to the use of a laboratory mixer of 5 liters of useful capacity of LODIGE brand and of a laboratory sprayer.
  • the detergent powder was obtained by mixing 5% by weight of the compound according to the invention with a detergent reconstituted in the laboratory according to French standard NF C73171.
  • washing powder containing 5% of the compound according to the invention are spread over the surface of the liquid.
  • the tissue is taken out of the basin, rinsed for 30 seconds under the tap with tap water, then wrung out.
  • a white cotton sample is brought into contact on the one hand with an aqueous solution of TINOLUX BBS alone and on the other hand, with an aqueous solution of the detergent compound according to the invention, for 20 minutes at 35 ° C.
  • the difference between the measurements carried out gives the quantity of TINOLUX BBS absorbed on the tissue, in% compared to the quantity fixed in the case of the Tinolux solution alone, which serves as a reference.
  • a maturing step is then carried out with stirring for 20 minutes in an unsaturated atmosphere.
  • spectrophotometric measurements indicate that TINOLUX BBS is well fixed on cotton, and this at 85%.

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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP90403320A 1989-12-08 1990-11-23 Waschmittelzusatz auf der Basis eines Polyphosphats und eines optisch aktiven Mittels, Verfahren zu dessen Herstellung und seine Verwendung als Waschmittel Expired - Lifetime EP0437988B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8916242 1989-12-08
FR8916242A FR2655658B1 (fr) 1989-12-08 1989-12-08 Compose lessiviel a base d'un polyphosphate et notamment d'un agent optiquement actif, son procede de preparation et son utilisation en detergence.

Publications (3)

Publication Number Publication Date
EP0437988A2 true EP0437988A2 (de) 1991-07-24
EP0437988A3 EP0437988A3 (en) 1991-08-14
EP0437988B1 EP0437988B1 (de) 1996-06-19

Family

ID=9388286

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90403320A Expired - Lifetime EP0437988B1 (de) 1989-12-08 1990-11-23 Waschmittelzusatz auf der Basis eines Polyphosphats und eines optisch aktiven Mittels, Verfahren zu dessen Herstellung und seine Verwendung als Waschmittel

Country Status (3)

Country Link
EP (1) EP0437988B1 (de)
DE (1) DE69027523D1 (de)
FR (1) FR2655658B1 (de)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0637626A1 (de) * 1993-08-06 1995-02-08 Rhone-Poulenc Chimie Verwendung von Silikonaten in Maschinengeschirrspülmittelzusammensetzungen
FR2728583A1 (fr) * 1994-12-23 1996-06-28 Rhone Poulenc Chimie Compositions detergentes a base d'un copolymere silicate organomineral, utilisation dudit copolymere comme agent alcalin non corrosif et protecteur du verre et de la vaisselle
WO2002088292A1 (en) * 2001-04-27 2002-11-07 Unilever Plc Radical initiator composition
WO2005003277A1 (en) * 2003-06-18 2005-01-13 Unilever Plc Blue and red bleaching compositions
WO2011137440A1 (en) * 2010-04-30 2011-11-03 Battelle Memorial Institute Composition for easy to clean surfaces
WO2023076192A1 (en) * 2021-10-28 2023-05-04 Dow Silicones Corporation Solid laundry drainage aid composition

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9323250D0 (en) * 1993-11-11 1994-01-05 Unilever Plc Process for the production of a detergent composition

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2354381A1 (fr) * 1976-06-12 1978-01-06 Dow Corning Ltd Compositions detergentes contenant une substance antimousse
EP0018039A1 (de) * 1979-04-21 1980-10-29 THE PROCTER & GAMBLE COMPANY Gewebeweichmacherzusammensetzung
EP0057088A1 (de) * 1981-01-24 1982-08-04 THE PROCTER & GAMBLE COMPANY Detergenszusammensetzungen
EP0082456A2 (de) * 1981-12-18 1983-06-29 Hoechst Aktiengesellschaft Konzentrierte Vormischungen von Wäscheweichspülmitteln
EP0210114A1 (de) * 1985-07-15 1987-01-28 Rhone-Poulenc Chimie Träger für flüssige Komponenten, Antischaummittel und diese enthaltende Reinigungsmittel
EP0210731A2 (de) * 1985-07-25 1987-02-04 Dow Corning Limited Schaumkontrollmittel für Reinigungsmittel

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2354381A1 (fr) * 1976-06-12 1978-01-06 Dow Corning Ltd Compositions detergentes contenant une substance antimousse
EP0018039A1 (de) * 1979-04-21 1980-10-29 THE PROCTER & GAMBLE COMPANY Gewebeweichmacherzusammensetzung
EP0057088A1 (de) * 1981-01-24 1982-08-04 THE PROCTER & GAMBLE COMPANY Detergenszusammensetzungen
EP0082456A2 (de) * 1981-12-18 1983-06-29 Hoechst Aktiengesellschaft Konzentrierte Vormischungen von Wäscheweichspülmitteln
EP0210114A1 (de) * 1985-07-15 1987-01-28 Rhone-Poulenc Chimie Träger für flüssige Komponenten, Antischaummittel und diese enthaltende Reinigungsmittel
EP0210731A2 (de) * 1985-07-25 1987-02-04 Dow Corning Limited Schaumkontrollmittel für Reinigungsmittel

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0637626A1 (de) * 1993-08-06 1995-02-08 Rhone-Poulenc Chimie Verwendung von Silikonaten in Maschinengeschirrspülmittelzusammensetzungen
FR2708620A1 (fr) * 1993-08-06 1995-02-10 Rhone Poulenc Chimie Utilisation de siliconate dans des compositions détergentes pour le lavage automatique de la vaisselle.
FR2728583A1 (fr) * 1994-12-23 1996-06-28 Rhone Poulenc Chimie Compositions detergentes a base d'un copolymere silicate organomineral, utilisation dudit copolymere comme agent alcalin non corrosif et protecteur du verre et de la vaisselle
WO1996020268A1 (fr) * 1994-12-23 1996-07-04 Rhone-Poulenc Chimie Agent alcalin non corrosif protecteur du verre et de la vaisselle et composition detergente contenant ledit agent alcalin
WO2002088292A1 (en) * 2001-04-27 2002-11-07 Unilever Plc Radical initiator composition
WO2005003277A1 (en) * 2003-06-18 2005-01-13 Unilever Plc Blue and red bleaching compositions
WO2011137440A1 (en) * 2010-04-30 2011-11-03 Battelle Memorial Institute Composition for easy to clean surfaces
US8871845B2 (en) 2010-04-30 2014-10-28 Battelle Memorial Institute Composition for easy to clean surfaces
WO2023076192A1 (en) * 2021-10-28 2023-05-04 Dow Silicones Corporation Solid laundry drainage aid composition

Also Published As

Publication number Publication date
FR2655658A1 (fr) 1991-06-14
DE69027523D1 (de) 1996-07-25
EP0437988B1 (de) 1996-06-19
FR2655658B1 (fr) 1994-11-18
EP0437988A3 (en) 1991-08-14

Similar Documents

Publication Publication Date Title
FR2479256A1 (fr) Composition de blanchiment aqueuse
CN1060108A (zh) 稳定的消毒去污微滴乳状液组合物
FR2619575A1 (fr) Compositions thixotropes aqueuses a base d'argile, leur procede d'utilisation pour nettoyer de la vaisselle, et procede pour ameliorer la stabilite de telles compositions
FR2537596A1 (fr) Detergent liquide puissant assouplissant les textiles
FR2574424A1 (fr) Procede d'activation du peroxyde d'hydrogene dans des bains de lavage ou de desinfection, compositions solides de lavage et de desinfection et utilisation de telles compositions dans des bains pour le lavage ou la desinfection des textiles
EP0437988B1 (de) Waschmittelzusatz auf der Basis eines Polyphosphats und eines optisch aktiven Mittels, Verfahren zu dessen Herstellung und seine Verwendung als Waschmittel
EP0425369B1 (de) Waschmittelzusammensetzung, Verfahren zu deren Herstellung und diese enthaltendes Waschmittel
FR2524902A1 (fr) Composition detergente adoucissante pour le linge, particules destinees a la fabrication de ces compositions et procede de fabrication de ces compositions
LU86731A1 (fr) Composition nettoyante liquide aqueuse thixotrope analogue a un gel et procede l'utilisant pour laver de la vaisselle en lave-vaisselle automatique
LU86227A1 (fr) Detergent et composition detergente liquides assouplissant les tissus pour gros lavages contenant de la bentonite
EP0165115A1 (de) Reinigungsmittelzusammensetzung zum Bleichen durch Photoaktivierung und deren Anwendungsverfahren
EP0414581B1 (de) Bei niedrigen Temperaturen wirksame Bleichmittelzusammensetzungen für Textilien
CA2261090C (fr) Composition detergente pour lave-vaisselle contenant un agent anti-corrosif
EP0063512B2 (de) Bleichmittelaktivatorgranulate, deren Herstellung und Verwendung in Reinigungs- und Bleichmittelzusammensetzungen
EP0210114B1 (de) Träger für flüssige Komponenten, Antischaummittel und diese enthaltende Reinigungsmittel
BE787276A (fr) Procede d'activation du blanchiment et compositions y relatives
EP0139547B1 (de) Granulierte Reinigungsmittel mit geringem Phosphatgehalt und Verfahren zu deren Herstellung
JPH10279411A (ja) カビ取り剤組成物
JPH0959675A (ja) 液体漂白剤組成物
EP1741451B1 (de) Verwendung zur Reinigung und zur Desinfizierung im Bereich der Milchherstellungshygiene
JP3410880B2 (ja) 液体漂白剤組成物
FR2542757A1 (fr) Composition de blanchiment et de lavage sans silicates hydrosolubles et procede utilisant cette composition
FR2720074A1 (fr) Composition détergente en poudre à base de percarbonate stabilisée par ajout de cogranulés silicate/carbonate.
EP0637626B1 (de) Verwendung von Silikonaten in Maschinengeschirrspülmittelzusammensetzungen
WO1996020268A1 (fr) Agent alcalin non corrosif protecteur du verre et de la vaisselle et composition detergente contenant ledit agent alcalin

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

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A2

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

AK Designated contracting states

Kind code of ref document: A3

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

17P Request for examination filed

Effective date: 19910906

17Q First examination report despatched

Effective date: 19940805

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

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

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 FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRE;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.SCRIBED TIME-LIMIT

Effective date: 19960619

Ref country code: ES

Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY

Effective date: 19960619

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19960619

Ref country code: GB

Effective date: 19960619

REF Corresponds to:

Ref document number: 69027523

Country of ref document: DE

Date of ref document: 19960725

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

Ref country code: SE

Effective date: 19960919

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

Ref country code: DE

Effective date: 19960920

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

Ref country code: BE

Effective date: 19961130

NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
GBV Gb: ep patent (uk) treated as always having been void in accordance with gb section 77(7)/1977 [no translation filed]

Effective date: 19960619

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

BERE Be: lapsed

Owner name: RHONE-POULENC CHIMIE

Effective date: 19961130

26N No opposition filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19970731

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST