EP1599568B1 - Objets en mousse de polyurethane hydrophile comprenant un compose antimicrobien - Google Patents

Objets en mousse de polyurethane hydrophile comprenant un compose antimicrobien Download PDF

Info

Publication number
EP1599568B1
EP1599568B1 EP04715941A EP04715941A EP1599568B1 EP 1599568 B1 EP1599568 B1 EP 1599568B1 EP 04715941 A EP04715941 A EP 04715941A EP 04715941 A EP04715941 A EP 04715941A EP 1599568 B1 EP1599568 B1 EP 1599568B1
Authority
EP
European Patent Office
Prior art keywords
cleaning article
article
cleaning
quaternary ammonium
polyurethane composition
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.)
Expired - Lifetime
Application number
EP04715941A
Other languages
German (de)
English (en)
Other versions
EP1599568A1 (fr
Inventor
Farid Ahmad Reckitt Benckiser Inc. NEKMARD
Diane Joyce Burt
James Chi-Cheng Feng
Paul Hermann
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.)
Reckitt Benckiser LLC
HH Brown Shoe Technologies Inc
Original Assignee
Reckitt Benckiser LLC
HH Brown Shoe Technologies Inc
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
Priority claimed from GB0317198A external-priority patent/GB0317198D0/en
Priority claimed from GB0321869A external-priority patent/GB2406099A/en
Application filed by Reckitt Benckiser LLC, HH Brown Shoe Technologies Inc filed Critical Reckitt Benckiser LLC
Publication of EP1599568A1 publication Critical patent/EP1599568A1/fr
Application granted granted Critical
Publication of EP1599568B1 publication Critical patent/EP1599568B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial 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
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • 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
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/049Cleaning or scouring pads; Wipes
    • 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
    • C11D3/3726Polyurethanes

Definitions

  • the present invention relates to articles having an antimicrobial benefit. More particularly the present invention relates to hydrophilic foam articles having an antimicrobial benefit.
  • cleaning articles which are used a number of times are used a breeding ground for undesirable bacteria and other microorganisms. Such include gram positive microorganisms as well as gram negative microorganisms.
  • the cleaning article indeed may be an incubator for such undesired microorganisms.
  • such cleaning articles are maintained in a moist state at a generally room temperature (approx. 20°C) environment, such typically are also suitable conditions for maintaining the viability of such microorganism.
  • room temperature approximately 20°C
  • the growth of the undesired micro-organisms increases the amount of these microorganisms which may come into contact with both the user, and with the surface to be treated upon the next use of the cleaning article.
  • US Patent 5091102 describes a substantially flexible dry matrix and the result and article capable of cleaning a surface by removing dust and/or organic film and rendering the surface substantially static-free, suitable for use as a garment, air filter or mat, wherein the dry matrix is uniformly coated with an amount of treatment solution sufficient to allow the matrix to retain its substantially dry characteristics, said treatment solution comprising between about 25% and 75% of at least one glycol compound, between about 0.2% and 60% of a cationic surfactant, an antimicrobial compound and optionally up to about 45% of a nonionic surfactant.
  • the foamed polyurethane composition may be used solely as hydrophilic foams providing an antimicrobial benefit, as well as in forming cleaning articles which may consist wholly of, or only partially of the foamed polyurethane composition which exhibits an antimicrobial benefit.
  • the polyurethane foam compositions of the invention is hydrophilic, and is capable of absorbing water, as well as containing and releasing a quaternary ammonium compound having germicidal properties.
  • the foamed polyurethane composition are advantageously formed of a polyurethane prepolymer composition which is used to form a foamed article, especially a foamed article having hydrophilic properties.
  • the selection of the polyurethane prepolymer is not critical and it is expected that any of a variety of known and commercially available polyurethane prepolymers may be used.
  • the hydrophilic polyurethane foam compositions of the present invention are prepared using an isocyanate-capped polyether prepolymer. Isocyanate-capped polyether prepolymers such as those disclosed in U.S. Pat. No. 4,137,200 are suitable for use in the present invention. These prepolymers have a defined average isocyanate functionality greater than 2.
  • the polyurethane prepolymer is foamed in the presence of an aqueous component, preferably water, in the conventional manner known in the art.
  • the aqueous component may also be a water slurry or suspension, a water emulsion, or a water solution having water soluble materials disposed therein.
  • the reaction mixture which contains at least the polyurethane prepolymer, and a quaternary ammonium compound having germicidal properties.
  • the reaction mixture typically contains further constituents which take part in reaction whereby the polyurethane foams which exhibit an antimicrobial benefit are formed.
  • the alkyl substituents may be long-chain alkyl, long-chain alkoxyaryl, long-chain alkylaryl, halogen-substituted long-chain alkylaryl, long-chain alkylphenoxyalkyl, arylalkyl, etc.
  • the remaining substituents on the nitrogen atoms other than the abovementioned alkyl substituents are hydrocarbons usually containing no more than 12 carbon atoms.
  • the substituents R 1 , R 2 , R 3 and R 4 may be straight-chained or may be branched, but are preferably straight-chained, and may include one or more amide, ether or ester linkages.
  • the counterion X may be any salt-forming anion which permits water solubility of the quaternary ammonium complex.
  • Exemplary quaternary ammonium salts within the above description include the alkyl ammonium halides such as cetyl trimethyl ammonium bromide, alkyl aryl ammonium halides such as octadecyl dimethyl benzyl ammonium bromide, N-alkyl pyridinium halides such as N-cetyl pyridinium bromide, and the like.
  • Particularly useful quaternary germicides include compositions which include a single quaternary compound, as well as mixtures of two or more different quaternary compounds.
  • Such useful quaternary compounds are available under the BARDAC®, BARQUAT®, HYAMINE®, LONZABAC®, and ONYXIDE® trademarks, which are more fully described in, for example, McCutcheon's Functional Materials (Vol. 2), North American Edition, 1998 , as well as the respective product literature from the suppliers identified below.
  • BTC® 65 is a commercially available preparation which is described to contain in 50%wt, of a C 12 -C 16 alkyl dimethyl benzyl ammonium chlorideprovided in an aqueous alcoholic carrier wherein water comprises 46%wt, of the commercial preparation, and ethanol comprises the remaining 4%wt, of the commercial preparation.
  • BTC® 2125M90 is a commercial available preparation which is described to contain 45%wt, of a C 12 -C 16 dimethyl benzyl ammonium chloride, 45%wt. of a C 12 -C 18 alkyldimethyl(ethylbenzyl) ammonium chloride, 4%wt. water, 3%wt. ethanol, and the remaining balance of 3%wt.
  • a further class of nonionic surfactants are primary and secondary linear and branched alcohol ethoxylates, such as those based on C 6 -C 18 alcohols which further include an average of from 2 to 80 moles of ethoxylation per mol of alcohol.
  • These examples include the Genapol® UD (ex.
  • nonionic surfactant constituent when present, may comprise two or more nonionic surfactants.
  • the nonionic surfactant is present in the compositions of the present invention in an amount of from about 0.1 % to about 10% by weight, more preferably is present in an amount of from about 1 -5%wt., and most preferably in an amount of from about 1-3.5%wt.
  • the lower alkanol of such alkanotammonium will normally be of 2 to 4 carbon atoms and is preferably ethanol.
  • R 1 is a C 12 - C 15 alkyl
  • n is from about 7 to about 13
  • M is an alkali metal counterion.
  • exemplary amphoteric surfactants include one or more water-soluble betaine surfactants which may be represented by the general formula: wherein: R 1 is an alkyl group containing from 8 to 18 carbon atoms, or the amido radical which may be represented by the following general formula: wherein R is an alkyl group having from 8 to 18 carbon atoms, a is an integer having a value of from 1 to 4 inclusive, and R 2 is a C 1 -C 4 alkylene group.
  • water-soluble betaine surfactants include dodecyl dimethyl betaine, as well as cocoamidopropylbetaine.
  • a further constituent which is optionally, but in certain cases desirably included in the foamed polyurethane compositions of the invention are one or more organic solvents which provides both a solvency function, as well as an anti-foaming function.
  • organic solvents can be virtually any organic solvent material.
  • silane compund also be included in the reaction mixture containing the polymer precursor.
  • the silanes are useful as coupling agents for the bulking agents, particularly where such bulking agents are minerals and thereby facilitate the incorporation of the bulking agents into the three dimensional structure of the polyurethane foams.
  • a cleaning article which exhibits an antimicrobial benefit
  • the foamed polyurethane article comprises at least one layer of a fibrous substrate bonded to a sponge formed from the foamed polyurethane composition, and preferably comprises a foamed polyurethane composition layer layered in register and between two fibrous substrate layers.
  • Nonwoven fibrous substrates may be a combination of wood pulp fibers and textile length synthetic fibers formed by well known dry-form or wet-lay processes. Synthetic fibers such as rayon, nylon, orlon and polyester as well as blends thereof can be employed, with or without fibers obtained from naturally occurring sources, e.g., wood pulp fibers, cellulose and the like. In certain embodiments, the wood pulp fibers should comprise about 30 to about 60 percent by weight of the nonwoven fabric, preferably about 55 to about 60 percent by weight, the remainder being synthetic fibers. The wood pulp fibers provide for absorbency, abrasion and soil retention whereas the synthetic fibers provide for substrate strength and resiliency.
  • Synthetic fibers such as rayon, nylon, orlon and polyester as well as blends thereof can be employed, with or without fibers obtained from naturally occurring sources, e.g., wood pulp fibers, cellulose and the like.
  • the wood pulp fibers should comprise about 30 to about 60 percent by weight of the nonwoven fabric, preferably about 55 to about 60 percent by weight
  • a particularly preferred embodiment of a cleaning article according to the invention is a multilayered cleaning article which comprises a layer of the foamed polyurethane composition providing an antimicrobial benefit layered in register and between two fibrous substrate layers, particularly where one of said fibrous substrate layers is constructed to provide an abrasive effect, while the other said fibrous substrate layer includes a quilted pattern.
  • Such an embodiment provides dual-function in that the abrasive layer may be used to improve the removal of soils or other materials on hard surfaces, while the opposite layer provides good water absorption and an attractive appearance. While any bonding means can be used, inter alia, stitching, adhesive, and the like, conveniently the two fibrous substrate layers are bonded to the intermediate polyurethane foam layer during the in-situ polymerization of the polyurethane foam.
  • the cleaning article would first be moistened with water or with any other cleaning composition and used to wipe the cutting board or cutting surface, thereafter it is contemplated that it would be rinsed in water, wrung to remove a majority of the water entrained within the sponge, and thereafter used to manually wash the dishes. Due to the rapid contact kill, most, if not all of the undesired micro-organisms which may come into contact from the cutting board or cutting surface and into the cleaning article would be destroyed or deactivated prior to coming into contact with the dishes to be manually washed particularly when the protocol of an intermediate rinsing step is practiced as outlined above.
  • a reaction mixture is formed from two components, the first component being the polyurethane prepolymer composition, e.g., HYPOL JT6000, and the second component being a premixture of the remaining constituents.
  • the second component was conveniently formed by combining its constituent in appropriate measured amounts in a standard laboratory glass beaker using conventional laboratory stirrer to ensure homogeneity of the second component.
  • test sponge was used to wipe the inoculated bottom of Plate I (Petri dish) for 2-3 seconds. This step represented a periodic challenge with a microbiological bioburden (viable test bacteria dried onto surfaces/carriers which are wiped.)
  • This sequence was repeated several times utilizing the same test sponge, so that the performance of a test sponge over a sequence of days, with 10 rinse/squeeze cycles performed on each assay day, could be evaluated.
  • the sequence was performed on sequential calendar days, as well as non-sequential calendar days where days were omitted, e.g., wherein the testing was not performed over two weekend days, but resumed during the following work week.
  • the number of survivors present on the plates were quantitated and the resulted recorded.
  • the results indicated below indicate the averaged results for the 3 replicates of the test sponges.
  • the sequence of the days is indicated in order of calendar days, which may not be sequential.
  • the results in the column indicated as "L” indicated the number of colonies of surviving Enterobacter aerogenes present on the plate (Plate 2) onto which the liquid was eluted from the test sponge
  • the results in the column indicated as "W” indicated the number of survivors present on the plate (Plate 3) which was wiped with the test sponge
  • the results in the column indicated as "R” indicated the number of survivors present on the plate (Plate R) which was wiped in order to assay the redeposition of Enterobacter aerogenes.
  • test sponges As can be seen from the foregoing, the tested cleaning articles (test sponges) produced according to the inventive teaching exhibited a good residual antimicrobial benefit is retained even after the cleaning article has been rinse/squeeze cycled a large number of times.
  • a multilayered cleaning article as depicted on Figures 2A and 2B comprising a layer of a foamed polyurethane composition according to the invention layered in register with a first abrasive fibrous substrate layer was produced.
  • the second component was conveniently formed by combining its constituents in appropriate measured amounts in a standard laboratory glass beaker using conventional laboratory stirrer to ensure homogeneity of the second component.
  • the second component is first formed by first providing the water to a suitable vessel, using a laboratory stirrer the Wollastonite 325 is added until a suspension is formed, followed by the Silquest 1120 which is allowed to mix approximately 10-20 minutes a homogenous mixture is attained, followed by the Tomadol 91-6, then Pluronic F88, then fragrance, then dye, followed by the Dowanol DPnB, and ultimately the BTC 65 and following the addition of the final constituent mixing is allowed to continue for further 20 minutes.
  • the quantity of eluted germicidal quaternary ammonium compounds were evaluated by a standard analytical technique via titration utilizing a tetraphenylborate solution. Of course other analytical techniques may be used and are expected to provide comparable results.
  • a sheet of a non-woven fibrous substrate material (Dexter® 10494 having a "quilted” surface) was applied to a flat laboratory benchtop. Subsequently a reaction mixture was formed from two components, the first component being the polyurethane prepolymer composition, e.g., HYPOL JT6000, and the second component being a premixture of the remaining constituents all of which are identified on Table 4, following.
  • the second component was conveniently formed by combining its constituents in appropriate measured amounts in a standard laboratory glass beaker using conventional laboratory stirrer to ensure homogeneity of the second component.
  • FIG. 3A , 3B and 3C A further embodiment of tri-layered cleaning article 30 is depicted on Figures 3A , 3B and 3C .
  • a foamed polyurethane layer 32 layered in register and between a first abrasive fibrous substrate layer 34 and a second fibrous substrate layer 36 comprising a quilted pattern having raised regions 38 bounded by recessed regions 40 which recessed regions are bonded to the foamed polyurethane layer 32 while the raised regions 38 are not.
  • Such a construction defines cavities 42 between the surface of the foamed polyurethane layer 32 and the raised regions 38, as bounded by the portion of the recessed regions 40 of the fibrous layer 36 not adhered to the foamed polyurethane layer.
  • the resultant tri-layered cleaning article formed was cut into a hexagonal shape measuring 5 inches in maximum width, and 6 inches in maximum height, and the ultimate thickness of the flexible wiping article was approximately 2-8 millimeter, as depicted on Figures 3A , 3B and 3C .

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Detergent Compositions (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Medicinal Preparation (AREA)
  • Materials For Medical Uses (AREA)

Claims (11)

  1. Composition de mousse de polyuréthanne hydrophile comprenant :
    0,001 à 10 % en poids d'un ou plusieurs composés d'ammonium quaternaire ayant des propriétés germicides, généralement répartis dans l'ensemble de la composition,
    un constituant tensio-actif détersif consistant en ou plusieurs agents tensio-actifs non ioniques, cationiques, zwitterioniques et amphotères en une quantité qui ne dépasse pas environ 10 % en poids,
    dans laquelle l'agent tensio-actif non ionique est choisi parmi les produits de condensation de poly(oxyde d'alkylène) d'alkylphénols, les produits de condensation d'alcools aliphatiques avec 1 à environ 60 moles d'un oxyde d'alkylène, les éthoxylates d'alcools linéaires et ramifiés primaires et secondaires, les copolymères à blocs alkoxy, les alkylmonoglycosides, les alkylpolyglycosides et les oxydes d'amine,
    la composition de mousse de polyuréthanne hydrophile présentant une masse volumique d'au moins 0,25 g/cm3,
    formée par un procédé comprenant les étapes opératoires suivantes :
    fournir un mélange réactionnel comprenant au moins un prépolymère de polyuréthanne, ledit composé d'ammonium quaternaire ayant des propriétés germicides, et ledit constituant tensio-actif détersif consistant en un ou plusieurs agents tensio-actifs non ioniques, cationiques, zwitterioniques et amphotères ; et former ensuite la composition de mousse de polyuréthanne hydrophile qui, après au moins vingt-cinq (25) cycles de rinçage/essorage, présente une élution d'au moins environ 100 parties par million, de préférence d'au moins environ 150 parties par million, de composés d'ammonium quaternaire germicides dans le fluide exprimé de l'article par pressage ou torsion.
  2. Composition de mousse de polyuréthanne hydrophile selon la revendication 1, qui, après au moins cinquante (50) cycles de rinçage/essorage, présente une élution d'au moins environ 200 parties par million de composés d'ammonium quaternaire germicides dans le fluide exprimé de l'article par pressage ou torsion.
  3. Composition de mousse de polyuréthanne hydrophile selon la revendication 1, qui, après au moins quarante (40) cycles de rinçage/essorage, présente une élution d'au moins environ 300 parties par million de composés d'ammonium quaternaire germicides dans le fluide exprimé de l'article par pressage ou torsion.
  4. Article de nettoyage comprenant une composition de mousse de polyuréthanne hydrophile selon l'une quelconque des revendications précédentes.
  5. Article de nettoyage selon la revendication 4, dans lequel l'article de nettoyage comprend au moins une couche d'un substrat fibreux liée à une éponge formée à partir de la composition de mousse de polyuréthanne hydrophile.
  6. Article de nettoyage selon la revendication 4, dans lequel l'article de nettoyage comprend au moins deux couches d'un substrat fibreux liées à une éponge formée à partir de la composition de mousse de polyuréthanne hydrophile.
  7. Article de nettoyage selon l'une quelconque des revendications 4, 5 ou 6, qui présente, après au moins cinquante (50) cycles de rinçage/essorage, une élution d'au moins environ 200 parties par million des composés d'ammonium quaternaires germicides dans l'eau exprimée de l'article par pressage ou torsion.
  8. Article de nettoyage selon l'une quelconque des revendications 4 à 7, dans lequel l'épaisseur maximale de la couche de mousse de polyuréthanne présente dans un article de nettoyage a une épaisseur maximale ne dépassant pas environ 10 millimètres, lequel article de nettoyage présente, après au moins dix (10) cycles de rinçage/essorage, de préférence au moins vingt-cinq (25) cycles de rinçage/essorage, une élution d'au moins environ 200 parties par million de composés d'ammonium quaternaire germicides dans le fluide exprimé de l'article par pressage ou torsion.
  9. Procédé pour nettoyer et/ou assainir une surface nécessitant un traitement, lequel procédé comprend les étapes suivantes :
    fournir un article en mousse de polyuréthanne selon l'une quelconque des revendications 1 à 3 ou un article de nettoyage selon l'une quelconque des revendications 4 à 8, et mettre en contact ladite surface avec ledit article en mousse de polyuréthanne hydrophile pour y exercer un effet de nettoyage et/ou d'assainissement.
  10. Procédé pour la fabrication d'un article de nettoyage selon l'une quelconque des revendications 4 à 8, lequel procédé comprend les étapes opératoires suivantes :
    fournir un mélange réactionnel comprenant au moins un prépolymère de polyuréthanne, un ammonium quaternaire ayant des propriétés germicides et un constituant tensio-actif détersif, et
    former ensuite la composition de mousse de polyuréthanne hydrophile utilisée dans l'article de nettoyage.
  11. Article de nettoyage formé par le procédé selon la revendication 10.
EP04715941A 2003-03-05 2004-03-01 Objets en mousse de polyurethane hydrophile comprenant un compose antimicrobien Expired - Lifetime EP1599568B1 (fr)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US45215003P 2003-03-05 2003-03-05
US452150P 2003-03-05
GB0317198 2003-07-23
GB0317198A GB0317198D0 (en) 2003-07-23 2003-07-23 Foam articles having an antimicrobial benefit
GB0321869A GB2406099A (en) 2003-09-18 2003-09-18 Foam articles having an antimicrobial benefit
GB0321869 2003-09-18
PCT/GB2004/000843 WO2004078900A1 (fr) 2003-03-05 2004-03-01 Objets en mousse de polyurethane hydrophile comprenant un compose antimicrobien

Publications (2)

Publication Number Publication Date
EP1599568A1 EP1599568A1 (fr) 2005-11-30
EP1599568B1 true EP1599568B1 (fr) 2009-01-21

Family

ID=32966159

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04715941A Expired - Lifetime EP1599568B1 (fr) 2003-03-05 2004-03-01 Objets en mousse de polyurethane hydrophile comprenant un compose antimicrobien

Country Status (5)

Country Link
EP (1) EP1599568B1 (fr)
AT (1) ATE421569T1 (fr)
DE (1) DE602004019192D1 (fr)
ES (1) ES2320766T3 (fr)
WO (1) WO2004078900A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007296934B2 (en) * 2006-09-16 2013-09-19 Bayer Intellectual Property Gmbh Alkylpolyglycosides as stabilizers for pu foams

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006012149A2 (fr) 2004-06-24 2006-02-02 Century-Board Usa, Llc Installation de fabrication en continu d'articles tridimensionnels en mousse
US7794224B2 (en) 2004-09-28 2010-09-14 Woodbridge Corporation Apparatus for the continuous production of plastic composites
WO2007112104A2 (fr) 2006-03-24 2007-10-04 Century-Board Usa, Llc Matériaux composites en polyuréthanne
DE102006033934B4 (de) * 2006-07-21 2009-09-10 Smart Fiber Ag Selbstdesinfizierendes Haushaltstuch
RU2429285C2 (ru) * 2007-02-12 2011-09-20 ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи Композит с высокой мягкостью и большой толщиной изолирующего слоя для салфеток
DE102007016684A1 (de) * 2007-04-04 2008-10-09 Dr. Schumacher Gmbh Biologisch abbaubares Mehrschichtsystem
US8846776B2 (en) 2009-08-14 2014-09-30 Boral Ip Holdings Llc Filled polyurethane composites and methods of making same
US9481759B2 (en) 2009-08-14 2016-11-01 Boral Ip Holdings Llc Polyurethanes derived from highly reactive reactants and coal ash
AU2012318528A1 (en) 2011-10-07 2014-05-22 Boral Ip Holdings (Australia) Pty Limited Inorganic polymer/organic polymer composites and methods of making same
US9932457B2 (en) 2013-04-12 2018-04-03 Boral Ip Holdings (Australia) Pty Limited Composites formed from an absorptive filler and a polyurethane
WO2016018226A1 (fr) 2014-07-28 2016-02-04 Crocco Guy Utilisation d'agents réfrigérants évaporatifs pour fabriquer des composites de polyuréthane chargés
US9752015B2 (en) 2014-08-05 2017-09-05 Boral Ip Holdings (Australia) Pty Limited Filled polymeric composites including short length fibers
WO2016118141A1 (fr) 2015-01-22 2016-07-28 Boral Ip Holdings (Australia) Pty Limited Composites de polyuréthanne hautement chargés
WO2016195717A1 (fr) 2015-06-05 2016-12-08 Boral Ip Holdings (Australia) Pty Limited Composites de polyuréthane chargés à charges légères
US20170267585A1 (en) 2015-11-12 2017-09-21 Amitabha Kumar Filled polyurethane composites with size-graded fillers

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2974134A (en) 1957-12-02 1961-03-07 Universal Oil Prod Co Surface active glucose ethers
US3219656A (en) 1963-08-12 1965-11-23 Rohm & Haas Alkylpolyalkoxyalkyl glucosides and process of preparation therefor
US3283357A (en) * 1964-10-06 1966-11-08 Michigan Tool Co Disinfecting cleansing pad
US3598865A (en) 1968-02-07 1971-08-10 Atlas Chem Ind Polyglycosides and process of preparing mono and polyglycosides
US3640998A (en) 1969-06-18 1972-02-08 Richard C Mansfield Alkylene oxide adducts of alkyloligosaccharides and their mixtures with alkylene oxide adducts of bord alkyl glucosides and alkanols
US3707535A (en) 1969-07-24 1972-12-26 Atlas Chem Ind Process for preparing mono- and polyglycosides
US3772269A (en) 1969-07-24 1973-11-13 Ici America Inc Glycoside compositions and process for the preparation thereof
US3839318A (en) 1970-09-27 1974-10-01 Rohm & Haas Process for preparation of alkyl glucosides and alkyl oligosaccharides
US3974138A (en) 1972-12-15 1976-08-10 Ici United States Inc. Method of preparing butyl polyglycosides
US4137200A (en) 1973-10-09 1979-01-30 W. R. Grace & Co. Crosslinked hydrophilic foams and method
US4223129A (en) 1978-09-01 1980-09-16 A. E. Staley Manufacturing Company Continuous process for making alkyl aldosides from starch or other carbohydrates
US4389448A (en) 1980-11-21 1983-06-21 Beecham Products Patterned dryer added fabric conditioning articles
US4476251A (en) 1983-11-01 1984-10-09 Olin Corporation Polyurethane foam having cleaning and germicidal activities
US4528106A (en) 1983-11-14 1985-07-09 Olin Corporation Glucoside surfactants
US4847089A (en) * 1986-07-16 1989-07-11 David N. Kramer Cleansing and distinfecting compositions, including bleaching agents, and sponges and other applicators incorporating the same
US5091102A (en) 1988-11-15 1992-02-25 Nordico, Inc. Method of making a dry antimicrobial fabric
JPH0940906A (ja) * 1995-07-28 1997-02-10 Toyoda Gosei Co Ltd インテグラルスキンフォーム成形品
GB9706714D0 (en) 1997-04-02 1997-05-21 Reckitt & Colman Inc Improvements in or relating to organic compositions
GB9706713D0 (en) 1997-04-02 1997-05-21 Reckitt & Colman Inc Improvements in or relating to organic compositions
GB9713023D0 (en) 1997-06-20 1997-08-27 Reckitt & Colmann Prod Ltd Improvements in or relating to the cleansing of surfaces

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007296934B2 (en) * 2006-09-16 2013-09-19 Bayer Intellectual Property Gmbh Alkylpolyglycosides as stabilizers for pu foams

Also Published As

Publication number Publication date
WO2004078900A1 (fr) 2004-09-16
ES2320766T3 (es) 2009-05-28
EP1599568A1 (fr) 2005-11-30
DE602004019192D1 (de) 2009-03-12
ATE421569T1 (de) 2009-02-15

Similar Documents

Publication Publication Date Title
US8188029B2 (en) Hydrophilic polyurethane foam articles comprising an antimicrobial compound
EP1599568B1 (fr) Objets en mousse de polyurethane hydrophile comprenant un compose antimicrobien
US6306810B1 (en) Hard surface cleaning and disinfecting compositions comprising fluorosurfactants
EP1788070B1 (fr) Compositions de nettoyage et de désinfection de surface dure
US7189686B2 (en) Water soluble sachet containing hard surface cleaner
CA2362219C (fr) Compositions nettoyantes et desinfectantes pour surfaces dures
US20100206328A1 (en) Alkaline Hard Surface Cleaning Composition
EP1523545B1 (fr) Nettoyants pour surfaces dures
EP3783089B1 (fr) Composition antimicrobienne comprenant un polymère de polyvinylpyrrolidone alkylé
US7030078B2 (en) Hard surface cleaning and disinfecting compositions comprising a tristyrylphenolethoxylate
GB2406099A (en) Foam articles having an antimicrobial benefit
EP1963472B1 (fr) Améliorations de, ou liées à des, préparations organiques
EP1812541B1 (fr) Ameliorations apportees a des compositions organiques ou relatives a ces dernieres

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

17P Request for examination filed

Effective date: 20050926

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL LT LV MK

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20051223

17Q First examination report despatched

Effective date: 20051223

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

RIN1 Information on inventor provided before grant (corrected)

Inventor name: NEKMARD, FARID AHMADRECKITT BENCKISER INC.

Inventor name: HERMANN, PAUL

Inventor name: BURT, DIANE JOYCE

Inventor name: FENG, JAMES CHI-CHENG

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 602004019192

Country of ref document: DE

Date of ref document: 20090312

Kind code of ref document: P

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2320766

Country of ref document: ES

Kind code of ref document: T3

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 FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20090121

NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

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: 20090121

Ref country code: FI

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: 20090121

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

Ref country code: AT

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: 20090121

Ref country code: PL

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: 20090121

Ref country code: SE

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: 20090421

Ref country code: PT

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: 20090622

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

Ref country code: BE

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: 20090121

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

Ref country code: DK

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: 20090121

Ref country code: CZ

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: 20090121

Ref country code: EE

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: 20090121

Ref country code: MC

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

Effective date: 20090331

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

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

Ref country code: RO

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: 20090121

Ref country code: SK

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: 20090121

26N No opposition filed

Effective date: 20091022

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

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

Ref country code: CH

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

Effective date: 20090331

Ref country code: BG

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: 20090421

Ref country code: IE

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

Effective date: 20090301

Ref country code: LI

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

Effective date: 20090331

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

Ref country code: GR

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: 20090422

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

Ref country code: LU

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

Effective date: 20090301

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

Ref country code: HU

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: 20090722

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

Ref country code: TR

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: 20090121

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

Ref country code: CY

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: 20090121

REG Reference to a national code

Ref country code: FR

Ref legal event code: CD

Owner name: RECKITT BENCKISER LLC

Effective date: 20111129

REG Reference to a national code

Ref country code: ES

Ref legal event code: PC2A

Owner name: RECKITT BENCKISER LLC.

Effective date: 20120210

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

Ref country code: ES

Payment date: 20130326

Year of fee payment: 10

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20150424

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

Ref country code: ES

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

Effective date: 20140302

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 13

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 14

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602004019192

Country of ref document: DE

Representative=s name: BARDEHLE PAGENBERG PARTNERSCHAFT MBB PATENTANW, DE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602004019192

Country of ref document: DE

Owner name: RECKITT BENCKISER LLC (N.D.GES.D. STAATES DELA, US

Free format text: FORMER OWNERS: RECKITT BENCKISER INC., PARSIPPANY, N.J., US; H.H. BROWN SHOE TECHNOLOGIES, INC., GREENWICH, CONN., US

Ref country code: DE

Ref legal event code: R081

Ref document number: 602004019192

Country of ref document: DE

Owner name: H.H. BROWN SHOE TECHNOLOGIES, INC., GREENWICH, US

Free format text: FORMER OWNERS: RECKITT BENCKISER INC., PARSIPPANY, N.J., US; H.H. BROWN SHOE TECHNOLOGIES, INC., GREENWICH, CONN., US

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 15

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

Ref country code: FR

Payment date: 20210112

Year of fee payment: 18

Ref country code: IT

Payment date: 20210211

Year of fee payment: 18

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

Ref country code: DE

Payment date: 20210216

Year of fee payment: 18

Ref country code: GB

Payment date: 20210217

Year of fee payment: 18

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602004019192

Country of ref document: DE

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

Effective date: 20220301

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: 20220301

Ref country code: FR

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

Effective date: 20220331

Ref country code: DE

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

Effective date: 20221001

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

Effective date: 20220301