EP1155109B1 - Desinfectant hypochloreux a couleur stable et procedes associes - Google Patents

Desinfectant hypochloreux a couleur stable et procedes associes Download PDF

Info

Publication number
EP1155109B1
EP1155109B1 EP00915847A EP00915847A EP1155109B1 EP 1155109 B1 EP1155109 B1 EP 1155109B1 EP 00915847 A EP00915847 A EP 00915847A EP 00915847 A EP00915847 A EP 00915847A EP 1155109 B1 EP1155109 B1 EP 1155109B1
Authority
EP
European Patent Office
Prior art keywords
dye
chlorine
solution
aqueous
source
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
EP00915847A
Other languages
German (de)
English (en)
Other versions
EP1155109A1 (fr
Inventor
Eddie D. Sowle
Darryl C. Bowling
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.)
Kay Chemical Co
Original Assignee
Kay Chemical Co
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 US09/501,876 external-priority patent/US20030059483A1/en
Application filed by Kay Chemical Co filed Critical Kay Chemical Co
Publication of EP1155109A1 publication Critical patent/EP1155109A1/fr
Application granted granted Critical
Publication of EP1155109B1 publication Critical patent/EP1155109B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047—Detergents in the form of bars or tablets
    • 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
    • C11D3/3955—Organic 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
    • C11D3/395—Bleaching agents
    • C11D3/3956—Liquid compositions
    • 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
    • C11D3/40—Dyes ; Pigments
    • 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
    • C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • 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
    • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02—Inorganic compounds
    • C11D7/04—Water-soluble compounds
    • C11D7/08—Acids
    • 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
    • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22—Organic compounds
    • C11D7/26—Organic compounds containing oxygen
    • C11D7/265—Carboxylic acids or salts thereof

Definitions

  • the invention relates to a solid concentrate composition which is shelf stable for a minimum of two years.
  • the invention also relates to a liquid or solid composition that combine a dye and a chlorine source resulting in unique cleaning or sanitizing properties with controlled, measured, acceptable and useful chlorine stability.
  • the invention also relates to methods for cleaning or sanitizing hard surfaces and for hand washing ware in a multibasin sink using at least a washing step involving an aqueous detergent solution followed by a sanitizing step involving an aqueous chlorine based sanitizer solution.
  • the composition may be used in a spray bottle for sanitizing hard surfaces.
  • Active halogen e.g. chlorine
  • materials have been available for bleaching, sanitizing and cleaning purposes for many years.
  • Such materials in the form of hypochlorite (NaOCI), chlorinated isocyanurate compounds, encapsulated chlorine sources, chlorinated tripolyphosphate, etc. have been used in single solutions or more commonly in alkaline, aqueous, powdered or solid materials to form active concentration of chlorine.
  • Such materials are commonly used to bleach clothing, clean or sanitize hard surfaces, and other generic destaining, antimicrobial or soil removing processes.
  • Such hard surfaces include ceramic, metal, plastic composite, surfaces that can be walls, floors, countertops, tables, chairs, food surface apparatus, etc. Such surfaces come into contact with a variety of soils and can also promote the growth of large populations of microorganisms. The removal of such soils and the reduction of microbial populations is an important goal in maintaining a high quality food service operation.
  • dishware tableware and kitchenware Another important type of hard surface is the surface of ware including dishware tableware and kitchenware.
  • the hand washing of dish and kitchenware is commonly achieved in a multibasin sink by first contacting soiled ware in an aqueous detergent solution with hand or mechanical agitation for the purpose of removing soil from the ware.
  • Such processes can also include other steps such as a prescraping step, a deliming step, a stain bleaching step or other conventional operations.
  • the ware is thoroughly rinsed typically with potable water.
  • the ware is then submerged in a sanitizing bath in a third basin and allowed to drain and permitted to dry.
  • a sanitizing step ensures that microbial populations are substantially reduced.
  • Oxidizing solutions are used until depleted of an effective chlorine content and are replaced when the concentration of the oxidizing species drops below a certain concentration typically below about 50 ppm active chlorine. Maintaining an effective concentration of the oxidizing species in the final sanitizing solution is important to maintain cleanliness, sanitization and a stain free condition in the ware. Active chlorine or OCl -1 concentration is typically monitored using indicator strips or test kits. Oxidizing solutions are highly active and can oxidize and decolorize a dye, used at conventional concentration, contained in the solution, rapidly often in an amount of time less than about 15 minutes.
  • a granular liquid or gelled warewashing detergent comprising a source of alkalinity such as a silicate, a builder, a surfactant and other warewashing components can be made stable in the presence of 0.01 to about 5 % of available chlorine from a chlorine bleach and a specifically disclosed yellow colorant or dye.
  • Choy et al. U.S. Patent No. 5,376,297 disclose thickened aqueous hard surface cleaning compositions containing a colloidal alumina thickener in combination with hard surface cleaner compositions such as a surfactant, a buffer, solvents, etc.
  • the thixotropic hard surface cleaner contains a source of oxidative chlorine and can contain a dispersible pigment. Wise, U.S. Patent No.
  • 5,384,061 discloses an aqueous thickened liquid or gel typically automatic warewashing detergent composition and can contain a dye in the presence of sodium hypochlorite.
  • Choy and Wise fail to disclose the sanitizing of ware in a third sink basin.
  • Kitko U.S. Patent No. 4,248,827, discloses a toilet sanitizing composition which produces hypochlorite ion in solution and contains a water soluble bleachable dye that provides a transitory visual signal. The dye is oxidized to a colorless state within 5 seconds to 15 minutes.
  • Cosentino et al. U.S. Patent No. 5,279,735, discloses a stable colored peracetic acid solution which contains a dye indicating its presence.
  • Sumi et al., JP-A-5140590 disclose a detergent composition that cleans and sanitizes in a single step and develops color upon dilution. Color duration is controlled by dye concentration, which results in solution color lasting from 2 to 12 minutes depending on solution temperature.
  • the stable dye may act as an indicator of active halogen concentration or content.
  • the formulation, dye type and constituent concentrations can be adjusted such that the presence of color is indicative of a proper sanitizing solution.
  • the bleaching, sanitizing, cleaning properties of the sanitizer use solution is consumed over a useful period of time, the solution loses color indicating the possible consumption of active chlorine and the need for a new sanitizer use solution.
  • a further need for acid powdered materials having a chlorine source in a stable dye that can be diluted into a use solution having the unique chlorine indicator is a long term goal of the industry.
  • Restaurant personnel need to know when a reasonable time has elapsed, indicating that a new solution is needed in order to maintain proper sanitization.
  • Such a time period to be useful is no less than 15 to 30 minutes and is typically greater than 2 but less than 24 hours, preferably greater than 2 but less than 6 hours.
  • a unique liquid, solid unit or powdered composition comprising an encapsulated source of halogen, preferably chlorine, and an indicator dye formulated such that a use solution made by diluting the liquid or powdered composition results in an aqueous composition containing an active concentration of a halogen source that can be gauged, estimated or monitored by the depth of color in the solution.
  • a unique liquid, solid unit or powdered composition comprising a source of acid, an encapsulated source of halogen, preferably chlorine, and an indicator dye formulated such that a use solution made by diluting the liquid or powdered composition results in an acidic aqueous composition containing an active concentration of a halogen source that can be monitored by the depth of color in the solution.
  • this composition is shelf or storage stable for a minimum of two years.
  • the depth of color in such aqueous solutions can be used as an indicator of concentration of the active halogen species.
  • a hard surface cleaning or a hand warewashing method or process including a sanitizing step in which a chlorine based sanitizing solution with a dye used in the sanitizing step.
  • the sanitizer can be formulated with an active chlorine source and sufficient dye to survive a predetermined period.
  • the sanitizing solution made from the composition of the invention can also be stabilized using a near neutral or an acid pH in such a way that a soluble dye added to the sanitizer solution can survive and provide color to the sanitizing solution for a predetermined period of time.
  • Such a period of time is an amount of time sufficient to deplete greater than 50%, 60%, 75%, 90% or other predetermined depletion target for the chlorine based oxidant in the sanitizer solution.
  • a replenishment of the active chlorine or a new sanitizer use solution is required.
  • the loss or change in color indicates that the concentration of halogen has been reduced significantly and can be reduced to near ineffective levels. This indicates the need for a fresh solution.
  • Monitoring the solution color will allow the personnel to know at all times that a proper sanitizing solution is present. In the sink sanitizer basin, two to six hours is adequate and is a reasonable predetermined period of time.
  • the aqueous chlorine containing solutions of the invention can be prepared in two specific embodiments.
  • the active chlorine solution can be prepared with any arbitrary pH. Often such pH's are mildly or strongly alkaline. In such a case, an amount of dye is used such that the color of the solution is maintained, even in the presence of the active chlorine sanitizer for a predetermined period.
  • the rates of reaction between the dye and the chlorine based sanitizer can be easily measured at a defined alkaline pH and an amount of dye is added to the composition to ensure that the dye survives to the end of the predetermined period. Once the dye in the solution is depleted, then the solution can be replaced or refreshed with additional chlorine source and dye.
  • an alternate mode that if used at an an acid pH (pH less than 7) that the dyes are unusually stable. In such a mode, a substantially reduced dye concentration can be used while maintaining an effective color in the sanitizing solutions for the predetermined period of time.
  • active pH that the active chlorine species possess enhanced antimicrobial activity or sanitizing capacity. Whereas, in alkaline chlorine species, an effective killing of microorganisms can exist at concentrations of between 100 and 1000 ppm, at acid pH's the concentration of the material can be reduced as low as 50 ppm with maintaining effective antimicrobial action.
  • Such materials can be used in a variety of useful processes that use the unique qualities of the halogen source. Generally such processes involve removing stains, removing soil, or killing microbial populations on surfaces that require cleaning.
  • ware is commonly washed in a first sink with aqueous detergent and exposed to mechanical action to remove soil resulting in cleaned ware. After the first sink the ware can optionally be treated in subsequent sinks for a variety of purposes. Then the cleaned ware is rinsed in a potable water rinse and is contacted with the dye containing chlorine sanitizer in a subsequent sink or basin for sanitizing purposes.
  • the hard surface is contacted with the oxidative halogen bleach composition in an overall cleaning method.
  • the hard surface can be scraped, washed with a detergent solution, rinsed and sanitized with the solutions of the invention.
  • the solutions are diluted and placed into an applicator bottle having the dye visible through a translucent or transparent bottle.
  • the material is applied preferably with a spray device uniformly contacting the hard surface with 50 to 200 ppm of the active halogen sanitizer material.
  • the sanitizer can be wiped from the surface or simply allowed to dry.
  • the preferred oxidative halogen chlorine-based sanitizing solution comprises a major proportion of an aqueous medium, a soluble oxidative active chlorine or chlorine based sanitizer, and a soluble organic dye.
  • said solution is maintained at a pH less than 7, preferably between a pH of 2 to 6.5.
  • One solution that maximizes chlorine activity and user comfort obtains about 90 to 200 ppm active Cl 2 at a pH of about 5.5 to 7.
  • the concentration of hypochlorous acid (HOCI) is maximized while the concentration of hypochlorite (OCl -1 , usually NaOCl) is minimized.
  • Such a solution can be made from a powdered or solid concentrate or liquid co-systems comprising a diluent, a dye, a chlorine source and other ingredients including an acid or acid salt.
  • hypochlorite not hypochlorous acid is the major oxidative species that decolorizes dye in hypochlorite based sanitizers.
  • the change in pH permits the dye to survive a substantial period since the oxidative (OCl -1 ) species is at reduced concentrations when compared to alkaline (pH>8) solutions. While the strength or capacity for the solution to remove surface stains in the ware is somewhat reduced, the ability to sanitize ware surfaces is substantially increased.
  • the dye can survive an extended period of time in the sanitizing solution.
  • the dye can be selected and matched with an appropriate pH such that the dye is depleted of color after a reasonable amount of time, roughly simultaneously with the sanitizing solution being substantially depleted of oxidizing chlorine species.
  • the sanitizing solution remains at least some detectable color until the oxidative chlorine species is depleted or consumed by bleaching or sanitizing processes.
  • the term “ware” indicates dishware, pots and pans, flatware, glassware, metallic and plastic utensils, and other tools and containers common in institutional or commercial kitchen or restaurant environments.
  • the term “solid unit” refers to a circular, cylindrical, pyramidal, rectangular, octangular or other geometrically shaped solid block or object having a mass of greater than 2 grams, preferably 5-25 grams.
  • the term “solid unit” does not refer to a particulate or granulated solid or simple high viscosity liquids that retain some shape.
  • subsequent basin means that the basin follows the previous basin.
  • one or more basins can come between the first basin and a subsequent basin to provide other method steps prior to the sanitizing step.
  • the sanitizing basin is the last basin in the process. After ware contact with the sanitizing solution, the ware is typically not further contacted with an aqueous solution because even service water can contain some level of a microbial population that can contaminate the sanitized surface.
  • One aspect of the invention is a method of using a color stable hypochlorous acid sanitizer material in a mode that permits the operator to gauge the bleaching or sanitizing capacity of a hypochlorous acid sink contents using a dyestuff.
  • the quantity of dye combined with the active chlorine material in the claimed compositions is matched to the pH and chlorine concentration to give apparent or detectable dye color to the hypochlorite solution for a predetermined time. After the dye color disappears or is depleted, the active chlorine can be replaced or augmented with an added active chlorine and dye composition.
  • a second aspect of the invention is a chemical composition that can be used to form the color stable hypochlorous acid sanitizer materials used in the method discussed above.
  • Such compositions comprise an active chlorine source and a dye in an amount that can give apparent or detectable dye color to the hypochlorite solution for a predetermined time, such time selected to ensure at least 50 ppm active chlorine is present in the solution. After the dye color disappears or is depleted, the active chlorine can be replaced or augmented with added chlorine composition.
  • a third aspect of the invention is a is a solid unit in the form, for example, of a tablet or pellet composition that can be manufactured and used to form the aqueous color stable hypochlorous acid sanitizer materials of the compositions and in the methods set forth above.
  • Simple solid units such as tablets or pellets can be formulated to contain the active ingredients of the stable system.
  • one or more pellets or tablets of the active materials can be introduced into the appropriate sink or container to create the active materials.
  • certain forms of preferred dyes are compatible in long term storage in the presence of highly active chlorine based oxidizing agents or sanitizers. After the dye color disappears or is depleted, the active chlorine can be replaced or augmented with added chlorine composition.
  • the invention resides in a solid unit, liquid or powdered and solid compositions comprising a source of halogen and a dye.
  • the composition can contain an acid source to maintain the pH ⁇ 7.
  • the invention also resides a method for hand washing or cleaning ware in a step-wise fashion with a sanitizing step as a last step in the method.
  • the first step in such a method involves contacting ware with an aqueous solution of a detergent composition for the purpose of removing soil from the surface of the ware.
  • the invention also resides in a method for cleaning hard surfaces. The cleaning step reduces microbial population substantially in a sanitizing fashion.
  • the first step in such a method involves rinsing or scraping the hard surface followed by an application of the sanitizing material.
  • the sanitizing material can be left in place to dry or can be rinsed or wiped from the surface.
  • the sanitizing solution can contain an effective concentration of one or more active and inactive ingredients that interacts with the ware and soil to enhance the ability of the aqueous medium to remove soil species.
  • the ware can be exposed to mechanical action by dishwashing personnel who use pads, brushes, scrapers, etc. to remove soil.
  • the aqueous detergent solution can be maintained at a high temperature (40-80°C) to promote the cleaning action of the aqueous detergent. Such solutions are often replaced periodically when the detergent action is depleted by the presence of substantial quantities of proteinaceous and oily or fatty soils.
  • the ware Prior to contacting the ware in such an aqueous detergent step, the ware is often scraped, rinsed or pretreated to promote soil removal in the detergent step. Following the initial cleaning step, the ware can be rinsed in a potable water rinse to remove the remaining aqueous detergent solution that can contain some small proportion of soil.
  • the ware can be contacted with a variety of different compositions in subsequent sinks or basins.
  • One common step is a deliming step for the purpose of removing hard inorganic calcium or magnesium based coatings from the ware comprising hardness, cations and other materials in a film or coating.
  • Such a step is often an acid deliming step that can substantially brighten and clarify the appearance of glassware.
  • the ware can also be contacted in an aqueous rinse composition in a rinse station.
  • Such rinse compositions contain organic polymeric agents that promote rinsing of the ware.
  • a variety of other stations or steps can be used in the method for the purpose of providing enhanced cleaning, brightening the appearance of the glass or metal ware, preserving the color or appearance of plates and cups, destaining tea stains or coffee stains from coffee mugs or cups or a variety of other operational steps.
  • the hard surface or the ware is contacted with a sanitizing solution commonly comprising an active halogen or chlorine, based sanitizer composition.
  • the sanitizing solution is typically made from a solid unit, solid, powdered or liquid concentrate of a chlorine containing product by dissolving the material in water.
  • One preferred solid chlorine concentrate of the invention contains a powdered or granular dye, a particulate encapsulated chlorine source, an acid or acid salt dispersed in a substantially neutral alkali metal salt acting as a diluent or extender.
  • Useful salts include sodium sulfate, sodium phosphate, sodium chloride, and other similar available extender salt materials.
  • Sources of halogen, chlorine, used in the methods of the invention include oxidizing compositions capable of liberating an active halogen species, typically Cl 2 or OCl -1 or equivalent materials.
  • Suitable agents for use in the present methods include both liquids and solid forms of halogen preferably chlorine sources, for example, chlorine containing compounds such as solutions of chlorine, hypochlorite, chloramine, etc.
  • Preferred halogen releasing compounds include the alkali metal hypochlorite, alkali metal dichloroisocyanurate, chlorinated trisodium phosphate, monochloramine and dichloramine and the like.
  • Encapsulated chlorine sources may also be used having at least one encapsulating layer surrounding a core of a chlorine source. Such encapsulated chlorine sources have multiple encapsulating layers. Encapsulated chlorine source are disclosed in U.S. Pat. No. 4,681,914 and 5,213,705.
  • the most common chlorine based sanitizer composition comprises sodium hypochlorite derived form an encapsulated source or from aqueous hypochlorite or other liquid and powdered or solid chlorine sources.
  • Aqueous hypochlorite is typically sold in the form of an aqueous solution containing approximately 5-10 wt-% sodium hypochlorate.
  • Solid sources of chlorine include chlorinated isocyanurate powder or encapsulate.
  • Such materials having a high pH, can be diluted with water to form an oxidizing aqueous solution containing an oxidative species at a concentration of about 50 to about 300 ppm, preferably about 60 to 200 ppm most preferably 70 to 150 ppm of the oxidative species.
  • the method of the invention uses an aqueous sanitizing composition containing an oxidative chlorine bleach.
  • the aqueous rinse used in the method can be manufactured by diluting a liquid co-system, powdered, pelletized or solid chlorine bleach containing composition.
  • the composition contains a chlorine source, the soluble dye, optionally an acid source that is typically diluted by a liquid or solid diluent or stabilizer.
  • sufficient amount of a liquid or powdered concentrate is added to the sanitizing process basin. The material dissolves in the aqueous liquid, creating an effective concentration of HOCl and dye at an appropriate pH. The aqueous solution is used until the color is depleted and is replaced when needed.
  • the oxidative chlorine concentrate of the invention can contain either a liquid or solid source of halogen, liquid sources of halogen, bleach commonly comprise alkali metal such as sodium hypochlorite bleach. These materials are commonly available in aqueous solution in a variety of concentrations.
  • a variety of solid chlorine sources are also available such as chlorinated sodium tripolyphosphate, solid dichloroisocyanurate, calcium hypochlorite and others.
  • Such oxidizing agents are disclosed in Kirk-Othmer, Encyclopedia of Chemical Technology , Second Edition, Volume III, pp. 550-566.
  • a preferred source of chlorine comprises an encapsulated chlorine source. Such chlorine sources are shown in Olson et al., U.S. Patent Nos. 4,681,914 and 5,358,653.
  • the chlorine releasing substances suitable as the core material of the encapsulated active chlorine compound include chlorine components capable of liberating active chlorine species such as a free elemental chlorine or OCl - , under conditions normally used in warewashing processes.
  • Useful inorganic sources of chlorine include solid materials that yield hypochlorite in aqueous environments including lithium hypochlorite, calcium hypochlorite, etc.
  • Useful organic chlorine releasing compounds must be sufficiently soluble in water to have a hydrolysis constant (K) of about 10 -4 or greater. Those with K values below 10 -4 do not produce sufficiently high concentration of free available chlorine or other active chlorine species for effective bleaching.
  • hydrolysis constants of the N-chloro compounds range from 10 -10 to approximately 10 -3 .
  • the principle N-chloro compounds used in bleaching are the chlorinated isocyanurates, which are chlorimides.
  • Sodium dichloroisocyanurate dihydrate a preferred chlorine releasing substance suitable as the core substance of the present encapsulated active chlorine compound, is commercially available from Olin Chemicals, Stamford, Conn., as CDB-56TM; or as ACL-56TM; Monsanto Company, St. Louis, MO.
  • the chemical structure of this compound is represented by the formula (II) below: MCl 2 (NCO) 3 ⁇ 2H 2 O (II) wherein M is an alkali metal such as Na + , K + , etc.
  • the encapsulate typically has one, two or more coatings sufficient to reduce chlorine loss.
  • the innermost, chlorine releasing core of the encapsulated active chlorine compound of the present rinse aid concentrate is surrounded by an intermediate coating or spacer layer.
  • This intermediate coating is preferably inorganic and can comprise a filler or builder compound (or mixtures thereof) and provides a protective barrier or spacing between the innermost chlorine core and the organic or inorganic outer layer(s).
  • the outer layer can comprise inorganic builders or organic surfactants.
  • the encapsulated halogen source is present in the concentrate at a concentration of about 1 to 90 wt-%, preferably about 5 to 70 wt-%.
  • the chlorine concentrate compositions of the invention are typically combined with an acid source to provide in the final sanitizing solution a pH of less than about 7 to control and minimize the concentration of OCl -1 and maximize the concentration of HOCl.
  • an acid source to provide in the final sanitizing solution a pH of less than about 7 to control and minimize the concentration of OCl -1 and maximize the concentration of HOCl.
  • any normally liquid or normally solid acid source which will facilitate the formation of such low pH may be used in the composition of the invention.
  • a liquid aqueous material can contain either solid or liquid acid. Both organic and inorganic acids have been found to be generally useful in the present composition.
  • Organic acids useful in accordance with the invention include hydroxyacetic (glycolic) acid, citric acid, formic acid acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, gluconic acid, and itaconic acid, trichloroacetic acid, benzoic acid, among others.
  • Organic dicarboxylic acids such as oxalic acid, malonic acid succinic acid, glutaric acid, maleic acid, fumaric acid, adipic acid, terephthalic acid among others are also useful in accordance with the invention. Any combination of these organic acids may also be used intermixed or with other organic acids which allow adequate formation of the composition of the invention.
  • Inorganic acids useful in accordance with the invention include phosphoric acid, sulfuric acid, sulfamic acid, methylsulfamic acid, hydrochloric acid, hydrobromic acid, and nitric acid among others.
  • Powdered acid salts can also comprise a source of acid for the invention.
  • Such acid salts can comprise sodium hydrogen sulfate, sodium dihydrogen phosphate, monosodium citrate, monosodium tartrate, monosodium succinate and other similar powdered acid salt compositions.
  • These acids may also be used in combination with other inorganic acids or with those organic acids mentioned above.
  • Preferred acids for a powdered composition are solid or powdered inorganic or organic acid.
  • the acid source is present in the concentrate at a concentration of about 0 to 30 wt-%, preferably about 0.5 to 30 wt-%, most preferably 5 to 15 wt-%.
  • the chlorine concentrate of the invention can also contain common builders in an acid form such as sodium sulfate (Na 2 SO 4 ), sodium carbonate (Na 2 CO 3 ), trisodium phosphate, sodium bicarbonate (NaHCO 3 ) and other acid builder salts such as sodium dihydrogen phosphate, disodium hydrogen phosphate, potassium hydrogen tartrate, monosodium nitrilo triacetic acid and other such acid salts that can aid in forming an appropriate acid pH, provide mild buffering action and aid in sanitization.
  • the acid builder salts are present in the concentrate at a concentration of about 0 to 90 wt-%, preferably about 5 to 75 wt-%.
  • the sanitizing solution and the chlorine containing concentrate of the invention include a dye.
  • Such dyes can comprise common ordinary dyes or can also include indicator dye materials.
  • Dyes are typically intensely colored substances used at low concentration with a coloration of various substances. The visual properties of dyes are determined by their electronic transitions within the dye molecule. The shade or hue of the dye is determined by energy differences between states in the molecular orbitals. A large number of dyes of varying properties are known.
  • Dyes useful in this invention are typically acid compatible dyes that are stable in the presence of HOCI at the pH disclosed in the invention. Dyes that may have utility in the invention include anthraquinone dyes.
  • Useful dyes include such species as blue tetrazolium dye, brilliant blue G, brilliant blue R, brilliant cresol blue, brilliant sulfone red, brilliant yellow, bromcresol green, reactive blue No. 2, reactive red No. 2, reactive yellow No. 2, FD&C No. 40, FD&C No. 3, etc.
  • the dye is selected for ease in blending with the powdered chlorine source, the acid salts and the diluent or extender of the invention.
  • the dye should be used at a concentration such that the dye begins to fade as the concentration of the OCl -1 begins to be depleted from the sanitizing solution, while the HOC1 concentration remains.
  • the particle size of the dye material is important to maintain dye stability in the tablet or solid concentrates of the invention.
  • the dye particle having a particle size greater than 200 ⁇ m, preferably greater than about 400 ⁇ m, most preferably greater than 600 ⁇ m can be made in the form of a solid, powder or a solid unit concentrate and is stabilized to contact with the encapsulated chlorine source. Such a result is surprising in light of the highly active oxidizing capacity of the chlorine source and the sensitive nature of typical organic dye molecules.
  • the sanitizing solution can contain an organic indicator dye.
  • organic indicator dye Such substances reveal through color changes the degree of acidity or basicity of a solution.
  • Most indicators are weak organic acids or bases which exist in one or more structural form (tautomers) of which at least one form is colored.
  • the indicator dye has two colored species, the colors are substantially different and can be detected in solution. Intense colors are desirable so that the minimum concentration of indicator can be used.
  • the color can occur at a characteristic pH for each indicator. Care must be taken to use an indicator having an appropriate pH change.
  • Indicator dyes that can be used in the context of this invention include methyl violet, metacresol purple, thimole blue, tropeoline 00 (orange roman IV), bromphenol blue, methyl orange, bromcresol green, methyl red, orthophenol red, bromcresol purple and others that have substantial color within the pH of about 3 to about 7.
  • the sanitizing solution is free of any component that can react with the oxidizing species.
  • the sanitizing solution can contain other materials that can enhance the antimicrobial properties or the bleaching properties of the sanitizing solution. Such materials include other oxidative species, oxidation promoters, etc.
  • the dye is present in the concentrate at a concentration of about 0.001 to 0.5 wt-%, preferably about 0.05 to 0.3 wt-%.
  • the amount of dye is selected to ensure that the dye provides detectable color for the predetermined period, which period typically ensures that the solution contain at least 50 ppm active chlorine or, depending on circumstances, greater than about 100 ppm active chlorine.
  • One of ordinary skill in the art will have no trouble in formulating these materials with the appropriate amount of dye since the rate of reaction of dye with the chlorine species selected can be easily determined for the purpose of selecting dye concentrations for the concentrate materials.
  • the amount of dye needed for acid based sanitizer materials is roughly 10% of the amount required to maintain color in neutral or alkaline systems.
  • the ware is contacted, in the method of the invention, in a first basin or sink containing an aqueous detergent composition.
  • the aqueous detergent solution can comprise a variety of ingredients including anionic, nonionic or cationic surfactant materials, other ingredients, etc.
  • anionic surfactant useful for detersive purposes can also be included in the compositions hereof.
  • These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, C 9 -C 20 linear alkylbenzenesulfonates, C 8 -C 22 primary or secondary alkanesulfonates, C 8 -C 24 olefinsulfonates, sulfonated polycarboxylic acids prepared by sulfonation of the pyrolyzed product of alkaline earth metal citrates.
  • salts including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts
  • C 9 -C 20 linear alkylbenzenesulfonates C 8 -C 22 primary or secondary alkanesulfonates
  • C 8 -C 24 olefinsulfonates C 8 -
  • alkylpolyglycolethersulfates (containing up to 10 moles of ethylene oxide); alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleyl glycerols sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates, isethionates such as the acyl isethionates, acyl laurates, fatty acid amides of methyl tauride, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinates (especially saturated and unsaturated C 12 -C 18 monoesters) and diesters of sulfosuccinates (especially saturated and unsaturated C 6 -C 12 diesters), acyl sarcosinates; sulfates of alkylpolysacc
  • alkyl ester sulfonates Another type of anionic surfactant which can be utilized encompasses alkyl ester sulfonates.
  • Alkyl ester sulfonate surfactants hereof include linear esters of C 8- C 20 carboxylic acids (i.e., fatty acids) which are sulfonated with gaseous SO 3 according to "The Journal of the American Oil Chemists Society" 52 (1975), pp. 323-329.
  • Suitable starting materials would include natural fatty substances as derived from tallow, palm oil, etc.
  • Alkyl sulfate surfactants hereof are water soluble salts or acids of the formula ROSO 3 M wherein R preferably is a C 10 -C 24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C 10 -C- 20 alkyl component, more preferably a C 12 -C 18 alkyl or hydroxyalkyl, and M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium), or ammonium or substituted ammonium (e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations such as tetramethylammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
  • R preferably is a
  • Alkyl alkoxylated sulfate surfactants hereof are water soluble salts or acids of the formula RO(A) m SO 3 -M + wherein R is an unsubstituted C 10 -C 24 alkyl or hydroxy alkyl group having a C 10 -C 24 alkyl component, preferably C 12 -C 20 alkyl or hydroxyalkyl, more preferably C 12 -C 18 alkyl or hydroxyalkyl, A is an ethoxy or propoxy unit, m is greater than zero, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3, and M is H or a cation which can be, for example, a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium, etc.).
  • R is an unsubstituted C 10 -C 24 alkyl or hydroxy alkyl group having a C 10 -C 24 alkyl component, preferably C 12 -C 20 alkyl or hydroxyal
  • ammonium or substituted-ammonium cation Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
  • substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium cations and quaternary ammonium cations such as tetramethyl-ammonium and dimethyl piperdinium cations and those derived from alkylamines such as ethylamine, diethylamine, triethyl-amine, mixtures thereof, and the like.
  • nonionic detersive surfactants for purposes of this invention include the polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols.
  • the polyethylene oxide condensates are preferred. These compounds include the condensation products of alkyl phenols having an alkyl group containing from about 6 to about 12 carbon atoms in either a straight chain or branched chain configuration with the alkylene oxide.
  • the ethylene oxide is present in an amount equal to from about 5 to about 25 moles of ethylene oxide per mole of alkyl phenol.
  • Nonionic surfactants of this type include IgepalTM CO-630, marketed by the GAF Corporation; and TritonTM X-45, X-114, X-100, and X-102, all marketed by the Rohm & Haas Company.
  • Nonionic surfactants also include the condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide.
  • the alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms.
  • Particularly preferred are the condensation products of alcohols having an alkyl group containing from about 10 to about 20 carbon atoms with from about 2 to about 10 moles of ethylene oxide per mole of alcohol.
  • nonionic surfactants of this type include TergitolTM 15 ⁇ 5 ⁇ 9 (the condensation product of C 11 -C 15 linear alcohol with 9 moles ethylene oxide), TergitolTM 24-L-6 NMW (the condensation product of C 12 -C 14 primary alcohol with 6 moles ethylene oxide with a narrow molecular weight distribution), both marketed by Union Carbide Corporation; NeodolTM 45-9 (the condensation product of C 14 -C 15 linear alcohol with 9 moles of ethylene oxide), NeodolTM 23-6.5 (the condensation product of C 12 -C 13 linear alcohol with 6.5 moles of ethylene oxide), NeodolTM 45.7 (the condensation product of C 14 -C 15 linear alcohol with 7 moles of ethylene oxide), NeodolTM 45.4 (the condensation product of C 14 -C 15 linear alcohol with 4 moles of ethylene oxide), marketed by Shell Chemical Company, and KyroTM EOB (the condensation product of C 13 -C 15 alcohol with 9 moles ethylene oxide), marketed by The Procter
  • the condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol can also be used.
  • the hydrophobic portion of these compounds preferably has a molecular weight of from about 1500 to about 1800 and exhibits water insolubility.
  • the addition ofpolyoxyethylene moieties to this hydrophobic portion tends to increase the water solubility of the molecule as a whole, and the liquid character of the product is retained up to the point where the polyoxyethylene content is about 50% of the total weight of the condensation product, which corresponds to condensation with up to about 40 moles of ethylene oxide.
  • Examples of compounds of this type include certain of the commercially available PluronicTM surfactants, marketed by BASF.
  • Cationic detersive surfactants can also be included in detergent compositions of the present invention.
  • Cationic surfactants include the ammonium surfactants such as alkyldimethylammonium halogenides, and those surfactants having the formula: [R 2 (OR 3 ) y ][R 4 (OR 3 ) x ] 3 R 3 N + X - ; wherein R 2 is an alkyl or alkyl benzyl group having from about 8 to about 18 carbon atoms in the alkyl chain, each R 3 is selected from the group consisting of: -CH 3 CH 2 -, -CH 2 CH(CH 3 )-, -CHCH(CH 2 OH)-, -CH 2 CH 2 CH 2 - and mixtures thereof; each R 4 is selected from the group consisting of C 1 -C 4 alkyl, C 1 -C 4 hydroxylalkyl, benzyl ring structures formed by joining the two R 4 groups, - CH 2 CHOH--CHOHC
  • the detergent compositions of the present invention comprises a liquid carrier, e.g., water, preferably a mixture of water and a C 1 -C 4 monohydric alcohol (e.g., ethanol, propanol, isopropanol, butanol, and mixtures thereof), with ethanol being the preferred alcohol.
  • a liquid carrier e.g., water, preferably a mixture of water and a C 1 -C 4 monohydric alcohol (e.g., ethanol, propanol, isopropanol, butanol, and mixtures thereof), with ethanol being the preferred alcohol.
  • compositions hereof A wide variety of other ingredients useful in detergent compositions can be included in the compositions hereof, including other active ingredients, carriers, processing aids, dyes or pigments, perfumes, solvents for liquid formulations, hydrotropes (as described below), etc.
  • Liquid detergent compositions can contain water and other solvents.
  • Low molecular weight primary or secondary alcohols exemplified by methanol, ethanol, propanol, and isopropanol are suitable.
  • Monohydric alcohols are preferred for solubilizing surfactant, but polyols such as those containing from about 2 to about 6 carbon atoms and from about 2 to about 6 hydroxy groups (e.g., propylene glycol, ethylene glycol, glycerin, and 1,2-propanediol) can also be used.
  • the detergent compositions hereof will preferably be formulated such that during use in aqueous cleaning operations the wash water will have a pH of between about 6.5 and about 11, preferably between about 7.5 and about 10.5.
  • Liquid product formulations preferably have a (10% dilution) pH between about 7.5 and about 10.0, more preferably between about 7.5 and about 9.0 Techniques for controlling pH at recommended usage levels include the use of buffers, alkali, acids, etc:, and are well known to those skilled in the art.
  • a chlorine containing bath having an indicator dye can be made by introducing into water, a solid unit such as a tablet, a pellet or other small compressed solid cast unit or extruded material.
  • the unit containing a chlorine is formulated to contain solid active chlorine material and the indicator dye.
  • the solid unit can be configured with sufficient material to treat an appropriate amount of water to form the indicated chlorine containing aqueous solution.
  • the size of the tablet, pellet or solid unit can range from greater than 2 grams to include sizes that can be as much as 100 grams depending on the amount of water.
  • the materials are used such that a unit has about 2 to 50 grams preferably 2 to 20, typically 4 to 8 grams of material in a single unit and can be used to treat about 1 liter of water or more, a typical sink volume of 1 to 100 preferably 10 to 50 liters.
  • the preferred solid units of the invention typically contain a solid chlorine source and a dye.
  • Typical solid chlorine sources include sodium dichloroisocyanurate dihydrate, chlorinated sodium phosphate, calcium hypochlorite, chloramines and other well known and available sources of chlorine and solid particulate or granular form.
  • Useful dyes include those set forth above in the application.
  • the solid pellets of the invention can also contain solid organic or inorganic components that can control pH of the chlorine solution.
  • the physical form of the dye is important to the stability of the dye in contact with the chlorine source.
  • Most dyes comprise complex organic molecules that are easily oxidized by compounds such as active chlorine sources.
  • a dye composition in the form of a particle or granule, having a particle size greater than 200 ⁇ M, preferably greater than about 500 ⁇ M, most preferably greater than about 700 ⁇ M can be used in the solid unit and remain stable for indefinite periods.
  • the particle size of a granular dye reduces the tendency of the dye to react with the active chlorine material in the solid unit. This is particularly true in the dry systems made in this invention.
  • the solid units of the invention are typically made with little or no free water or water added. Free water within the solid unit can provide a medium for reaction between the chlorine source and the dye material, even if formulated or formed from a granular dye. Accordingly, the solid units of the invention have little or no free water present. Water can be present in the solid unit in the form of water of hydration as long as such water is not released from the hydration location into the solid unit for the purpose of providing a medium for reaction. Water of hydration, for example, of the sodium dichloroisocyanurate dihydrate remains securely bonded to the chlorinated molecule and does not typically act to reduce compatibility. Other hydrated materials can be used in the solid unit of the invention. For example, extender salt hydrates may be present in the solid unit for the purpose of diluting the chlorine source, modifying dissolution rates, changing the size of the solid unit for the purpose of acting as a binder for the solid unit or further purposes.
  • the weight ratio between the chlorine source and the dye will be typically about 10 to about 200 grams of chlorine source per gram of dye.
  • the solid units of the invention can be made using a variety of solids forming technology. The only limitation on such technology is the need to avoid forming substantial quantities of free water remaining in the solid unit. Accordingly, preferred modes for forming the solid unit of the invention include casting the solid units from a castable, typically non-aqueous liquid, or by forming pellets or tablets by compressing powder mixture in tablet or pelletizing equipment under sufficient pressure and in the pressure of optional binders to form a useful solid unit. In forming the solid units of the invention, a mold, a tablet or pellet press equipment can be used to form a tablet having dimensions of about 2 to 50 millimeters in diameter, preferably 5 to 25 millimeters in diameter. Tablet thicknesses can range from about 2 to 20 millimeters. Most preferred diameters range from about 10 to 25 millimeters. In a preferred embodiment the solid unit comprises a spheroid having a major dimension of about 5 to about 60 millimeters and one perpendicular dimension of about 1 to 50 millimeters.
  • a useful 20 millimeter tablet can be made using a tablet press that can exert 2 tons force to particulates in a tableting dye.
  • a quantity of a mixture of the solid chlorine source and granular dye can be placed manually or in an automated mode into the tablet dye and compressed for dwell time of 1 to 30 seconds to a pressure of 0,68948 ⁇ 10 7 to 20,68425 ⁇ 10 7 Pa (1/2 to 15 tons per square inch).
  • the tableting dyes can be entirely cylindrical or can have a concave or opaque top or bottom surface to obtain a desired tablet shape. Sufficient pressure is placed on the particulate to achieve a hardness of greater than about 344 738 Pa (50 psi), typically 413685,6 to 689476 Pa (60 to 100 psi).
  • the tablets of the invention can be made using conventional tableting technology.
  • dry, granular or powder material are combined in typical powder blending equipment to ensure any uniform mixture of ingredients that typically include the granular dichlorodiisocyanurate chlorine source, the dye in a granular form and often a processing aid or dye release material.
  • Any conventional tableter can be used that can form a table of the appropriate dimensions.
  • the preferred tablet dimensions is about 1.5 to 2.5 centimeters in diameter with a thickness of about 1 to 2 centimeters.
  • Typical processing conditions involve a tableting pressure of at least 5 tons or more, tablet formation occurring in 1 to 5 seconds, typically 2 to 3 seconds.
  • compositions and tablets of the invention can be used in a variety of ways.
  • the material can simply be added directly to a sink when the color is depleted.
  • the materials can be added from a dispenser that can dispense either a measured portion of the powdered material or a single tablet of the tableted materials.
  • the tablets can be shaped to fit in a tablet dispenser with a lock-out feature.
  • the shape of the tablets can be such that only the tablet shapes can fit the dispenser profile. In such a way, only the appropriate tablets can be placed into the dispenser to avoid either waste of material or hazardous combinations of ingredients.
  • Component #1 (wt-%) #2 (wt-%) #3 (wt-%) #4 (wt-%) #5 (wt-%) #6 (wt-%)
  • ACP 1 33.60 34.90 9.50 0 67.20 27.57 SAPP 2 14.10 56.40 25.70 14.1 28.24 0 anhydrous citric acid 2.11 8.40 0 26.6 4.20 5.97 FD&C Dye 3 0.14 0.20 0.04 0.07 0.28 0.20 propylene glycol 0.17 0.10 1.00 0.11 0.08 0.10 sodium sulfate 49.88 0 46.46 9.12 0 0 MSP 4 0 0 17.30 0 0 66.16 chlorinated TSP 5 0 0 0 50.0 0 0 1.
  • Encapsulated sodium dichloro-s-triazinetrione dihydrate 2. Sodium acid pyrophosphate. 3. FD&C red #40, FD&C blue #1, etc. 4. Monosodium phosphate. 5. Chlorinated trisodium phosphate.
  • Formulations 1 and 3 listed above were made and placed into a 120°F (49°C) oven for long term stability testing. The formulations were monitored weekly for available chlorine levels and for color stability. Duplicates were made of formulations and 3 which differed only in using non-encapsulated sodium dichloro-s-triazinetrione as the chlorine source. After 8 weeks, all of the formulations having encapsulated chlorine sources retained acceptable active levels. The two formulations lacking an encapsulated chlorine source lost their efficacy after only 1 week. The active chlorine source bleached the dye.
  • Example II Using Example II, a sanitizing solution containing 30 ppm chlorine and 10 ppm dye at pH about 7 provided active sanitizing with solution color lasting about two hours. At a lower pH, between 5 and 6, a sanitizing solution containing 30 ppm chlorine and 10 ppm dye lasted approximately four hours. In both cases, substantial sanitizing activity was observed without corrosion or chlorine gassing.
  • a sanitizing solution can be made visible based on the composition of the concentrate.
  • the length of time that the visibility or color of the solution lasts can be controlled by varying the percentages of the dye, the level of active and the pH/buffer component.
  • the pH/buffer component has the greatest effect, while the dye and active can be used for fine-tuning.
  • Example V involves a liquid co-system. This is a two-part system.
  • the first solution contains sufficient NaOCl into the sink to produce 100 ppm available chlorine and sufficient H 3 PO 4 to produce a pH between 5 and 6, 1.0% of FD&C RED Dye #40 and color lasting between 2 and 6 hours.
  • the second solution contains sufficient NaOCl in the sink to produce 100 ppm available chlorine, 20.0% of a 75% active aqueous H 3 P0 4 , 1.0% of FD&C RED Dye #40 and 79.0% of water. The color lasts for at least one hour.
  • a dye typically considered to be unstable in the presence of strong oxidants such as halogen bleaches, can remain stable for a sufficient period of time to be used as an indicator of an oxidative quality of the solution and/or the efficacy of a sanitizer solution.
  • the use of an encapsulated chlorine source in a powdered concentrate appears to be important in maintaining and extending the stability.
  • the stability permits the use of such a dye with such an oxidative halogen bleach in a hard surface sanitizing method and a hand warewashing method.
  • the ware In hand ware washing, the ware is first washed with a typical surfactant system and then sanitized in the dye containing halogen solution.
  • the indicator can be used to show the effective concentration of the chlorine source and can suggest the appropriate time for replacing the chlorine bleach solution at intervals which results in the efficient use of the sanitizer solution. If the solutions were replaced too early, the chlorine bleach materials can be wasted. If the solutions were replaced after too long an interval, solutions would be depleted of active chlorine species and would not bleach or sanitize the ware.
  • the overall process of the invention produces clean bleached and sanitized ware in a handwashing system without wasted chlorine bleach materials.
  • the bacterial efficacy of a sample must be equivalent to, or greater than, the 50 ppm chlorine standard to be certified by the USDA. Equivalency is met when the sample tubes have an absence in growth in as many tubes as the chlorine standard.
  • the five experimental sanitizers exhibited bactericidal efficacy approximating the expected results from chlorine standards prepared at those concentrations. Thus, while passing the Available Chlorine test against S. aureus , the sanitizer formulations showed no enhancement of antibacterial properties over those of our current formula as expected with this test.
  • Chlorine Based Sanitizer Chlorine ppm Source of Chlorine % Reduction pH Chlorine (ppm) Conc. 0 Time Chlorine (ppm) Conc. 4 Hours Chlorine (ppm) Conc. 24 Hours 10 CDB Chlorinated Isocyanurate 100.0000 4.55 9.9 8.5 5.67 10 CDB Chlorinated Isocyanurate 99.9999 4.55 9.9 8.5 5.67 30 CDB Chlorinated Isocyanurate 100.0000 4.78 26.9 22.69 19.85 30 CDB Chlorinated Isocyanurate 100.0000 4.78 26.9 22.69 19.85 12 Chlorinated TSP 100.0000 5.13 12.7 9.93 5.67 12 Chlorinated TSP 100.0000 5.13 12.7 9.93 5.67 Inoculum 2.2E+9 Control 21.8E+6
  • the tableted product produced in the Example was used in forming an active chlorine containing aqueous solution in a sink.
  • the solution is used over a period of 4 hours.
  • the solution is discarded after the dye disappears indicating that the typical lifetime of the solution has ended.
  • Example XVII Using the procedure of Example XVII, a 10 gram tablet was made using the following formulas. Ingredients A (wt%) B (wt%) Granular sodium dichloroisocyanurate dihydrate 99.56 97.57 FD&C #40 (Granular) 0.44 1.43 Sodium Stearate 0.0 1.0
  • Example XVII Using the procedure of Example XVII, a 6.8 gram tablet was made using the following formulas. Ingredients A (wt%) B (wt%) Granular sodium dichloroisocyanurate dihydrate 99.56 97.57 FD&C #40 (Granular) 0.44 1.43 Sodium Stearate 0.0 1.0
  • the tableted products of Example XVIII and XIX were used in a sanitizing solution at a ratio of one tablet in a 37,85 L (10 gallon) volume of water. The pH was about 6.0 and produced at least 100 ppm of active chlorine in the water until the dye color was depleted. The tablet was also tested for stability.
  • the materials lost no chlorine or dye activity over a six month period of storage at typical ambient conditions at ambient temperature of about 21-24°C (70-75°F) with ambient relative humidity.
  • the tablets had no substantial loss of chlorine or dye activity over five months held at a temperature between 44-53°C (112°-127°F).

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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Dans les entreprises de restauration, la plonge manuelle est généralement effectuée dans un évier à plusieurs compartiments. Dans un bassin la vaisselle est mise en contact avec une solution aqueuse d'un agent tensioactif. La vaisselle est rincée dans un autre bassin, puis désinfectée dans un troisième bassin au moyen d'une solution désinfectante. Des décolorants à base d'hypochlorite fortement oxydant, permettent, lorsque le pH est ajusté à une valeur convenable, de maintenir une capacité sensiblement désinfectante tout en ne décolorant pas des colorants sensibles à l'oxydation. Dans le procédé de l'invention, la solution désinfectante, ajustée à un pH inférieur à environ 7, contenant un colorant, permet de garder une coloration stable durant une période supérieure à la durée requise pour épuiser 90 % ou plus d'ion OCl-1 en solution. Il en résulte une indication satisfaisante de la présence de désinfectant actif sur la base de la couleur de la solution désinfectante.

Claims (41)

  1. Unité solide contenant du chlore actif, contenant une source de chlore et une source de colorant stable, l'unité solide comprenant :
    (a) de 10 à 200 parties en poids d'une source de chlore actif solide pour chaque partie de colorant ; et
    (b) une source de colorant, le colorant comprenant un colorant particulaire ayant une taille de particule minimale de 200 µm, l'unité solide ayant une plus grande dimension supérieure à 2 millimètres et un poids supérieur à 2 grammes, l'unité solide étant essentiellement exempte d'une quantité d'eau libre suffisante pour agir comme milieu réactionnel entre la source de chlore solide et le colorant.
  2. Unité solide selon la revendication 1, dans laquelle le colorant comprend un colorant ayant une taille de particule minimale de 500 microns environ et une densité inférieure à 0,9 g cm-3.
  3. Unité solide selon la revendication 1, dans laquelle l'unité solide comprend un comprimé cylindrique ayant un diamètre de 4 à 75 millimètres environ et une épaisseur de 1 à 25 millimètres environ.
  4. Unité solide selon la revendication 1, dans laquelle la source de chlore solide comprend un dichloroisocyanurate de métal alcalin dihydraté.
  5. Unité solide selon la revendication 1, dans laquelle l'unité solide comprend un sphéroïde ayant une plus grande dimension de 5 à 60 millimètres environ et une dimension perpendiculaire de 1 à 50 millimètres environ.
  6. Unité solide selon la revendication 4, dans laquelle la source de chlore solide comprend un dichloroisocyanurate de métal alcalin dihydraté encapsulé.
  7. Unité solide selon la revendication 1, dans laquelle le colorant comprend un colorant granulaire ayant une taille de particule supérieure à 600 µm environ et une densité inférieure à 0,85 g cm-3 environ.
  8. Procédé d'utilisation de l'unité solide selon la revendication 1 dans une opération de nettoyage ou d'assainissement, le procédé comprenant les étapes consistant à :
    (a) placer une unité solide dans un volume d'un liquide aqueux dans un récipient, le ratio en poids du solide sur la solution aqueuse étant de 0,1 à 20 grammes par litre d'eau, afin de former une solution de chlore actif colorée par un colorant ; et
    (b) mettre de la vaisselle en contact avec la solution aqueuse à base de chlore actif au cours des opérations de nettoyage ou d'assainissement pendant une durée allant jusqu'à 4 heures et, après la détection d'un changement de couleur, remplacer la solution aqueuse ou bien compléter la solution aqueuse avec une source de chlore supplémentaire.
  9. Composition particulaire formant une solution aqueuse contenant une source de chlore actif et un colorant, le concentré en poudre comprenant :
    (a) environ 1 à 90% en poids d'une source d'halogène encapsulée ; et
    (b) une quantité efficace de colorant ;
    (c) une source d'acide pour obtenir un pH inférieur à 7 dans la solution aqueuse,
    dans laquelle le concentré ne contient essentiellement pas d'eau libre, a une longue durée de conservation supérieure à un mois et, lorsqu'il est ajouté à un diluant aqueux, donne un colorant qui indique la présence d'une concentration en halogène actif pendant une durée prédéterminée.
  10. Composition selon la revendication 9, contenant un sel adjuvant acide qui est le cas échéant le sulfate de sodium, le carbonate de sodium, le phosphate trisodique, le bicarbonate de sodium ou des mélanges de ceux-ci.
  11. Composition selon la revendication 9, dans laquelle la concentration en colorant dans le concentré est ajustée de telle façon que la couleur du colorant change ou est appauvrie pendant une durée utile prédéterminée pendant laquelle la solution d'assainissement peut être utilisée pour son but prévu et maintient au moins 50 ppm de chlore actif.
  12. Composition de nettoyage ou d'assainissement liquide aqueuse contenant un colorant, dans laquelle la perte ou le changement de couleur indique une réduction de la concentration en chlore, le liquide comprenant une proportion majeure d'un diluent aqueux, et
    (a) une source d'acide ;
    (b) une quantité efficace d'un colorant pour obtenir une solution colorée pendant une durée prédéterminée ;
    (c) une quantité d'un agent de blanchiment halogéné efficace pour le nettoyage ou l'assainissement ;
    dans laquelle la solution aqueuse a un pH inférieur à 7 et la couleur du colorant est appauvrie ou modifiée avant que la concentration en halogène soit appauvrie à moins de 50 ppm de la solution.
  13. Composition selon la revendication 9 ou la revendication 12, dans laquelle la source d'halogène comprend une source de chlore.
  14. Composition selon la revendication 13, dans laquelle la source de chlore comprend un composé chloroisocyanurate.
  15. Composition selon la revendication 12, qui comprend également un sel adjuvant.
  16. Composition selon la revendication 14, dans laquelle la source de chlore comprend un dichloroisocyanurate de métal alcalin dihydraté encapsulé.
  17. Composition selon la revendication 9 ou la revendication 12, dans laquelle la source d'acide comprend un acide solide.
  18. Composition selon la revendication 9 et la revendication 12, dans laquelle le sel d'acide comprend le dihydrogénophosphate de sodium, l'hydrogénotartrate de sodium, l'hydrogénosulfate de sodium ou des mélanges de ceux-ci.
  19. Composition selon la revendication 12, dans laquelle le sel adjuvant comprend le sulfate de sodium, le carbonate de sodium, le phosphate trisodique, le bicarbonate de sodium ou des mélanges de ceux-ci.
  20. Composition selon la revendication 12, dans laquelle la concentration en colorant dans le concentré est ajustée de telle façon que la couleur du colorant change ou est appauvrie au cours d'une durée utile pendant laquelle la solution d'assainissement peut être utilisée pour son but prévu.
  21. Procédé de nettoyage ou d'assainissement de surfaces dures comprenant les étapes consistant à :
    a) mettre la surface dure en contact avec une solution aqueuse comprenant la composition de la revendication 9, afin de former une surface ayant le liquide aqueux comprenant une source d'halogène ; et
    (b) éliminer la source d'halogène liquide aqueuse.
  22. Procédé de lavage à la main de vaisselle dans un évier ayant deux ou plusieurs bacs en utilisant un colorant stable dans une composition aqueuse de nettoyage ou d'assainissement à base de chlore oxydant, le procédé comprenant les étapes consistant à :
    (a) mettre la vaisselle en contact avec un détergent aqueux dans un premier bac afin d'éliminer les salissures et produire de la vaisselle nettoyée ; et
    (b) mettre la vaisselle nettoyée en contact dans un autre bac avec une solution d'assainissement aqueuse comprenant une quantité efficace d'une source de chlore, la solution d'assainissement comprenant en plus un colorant qui est suffisamment stable dans la solution aqueuse pour maintenir au moins un peu de couleur détectable dans la solution d'assainissement après que plus de 90% des espèces oxydantes aient été consommées et, lorsque la solution devient claire ou change de couleur, un complément de chlore actif ou une nouvelle solution d'assainissement est nécessaire.
  23. Procédé selon la revendication 22, dans lequel la source de chlore comprend un hypochlorite de métal alcalin.
  24. Procédé selon la revendication 23, dans lequel l'agent d'assainissement à base d'hypochlorite comprend de l'hypochlorite de sodium.
  25. Procédé selon la revendication 22, dans lequel la source de chlore comprend un composé isocyanurate chloré qui génère un acide hypochloreux au pH.
  26. Procédé selon la revendication 22, dans lequel la vaisselle nettoyée est mise en contact avec un rinçage à l'eau potable afin de former une vaisselle nettoyée rincée avant de mettre la vaisselle nettoyée rincée en contact avec la solution d'assainissement.
  27. Procédé selon la revendication 22, dans lequel la solution d'assainissement aqueuse a un pH inférieur à environ 7, le pH étant choisi de telle façon que la concentration en OCl-1 est minimisée et la concentration en HOCl maximisée.
  28. Procédé selon la revendication 26, dans lequel la vaisselle nettoyée est mise en contact avec le rinçage aqueux pendant environ 1 à environ 30 secondes et la vaisselle nettoyée rincée est mise en contact avec la solution d'assainissement aqueuse pendant environ 1 à 30 secondes.
  29. Procédé selon la revendication 22, dans lequel la vaisselle est mise en contact avec une action mécanique dans le premier bac avec le détergent aqueux pendant une durée suffisante pour éliminer la majorité des débris d'aliments et la vaisselle nettoyée est mise en contact avec la solution d'assainissement aqueuse pendant environ 1 à environ 30 secondes.
  30. Procédé selon la revendication 22, dans lequel la concentration de la source de chlore est de 1 à 100 parties par million environ dans la solution.
  31. Procédé selon la revendication 22 et compositions selon les revendications 9 et 12, dans lesquels l'indicateur comprend un colorant FD & C n° 40.
  32. Procédé selon la revendication 22 et composition selon la revendication 9, dans lesquels l'indicateur comprend un colorant FD & C n° 3.
  33. Procédé selon la revendication 22, dans lequel, après l'étape d'assainissement, la vaisselle est laissée à sécher sans contact avec une action mécanique ou avec une solution aqueuse.
  34. Procédé selon la revendication 22, dans lequel la solution d'assainissement est préparée en diluant un solide en poudre comprenant :
    (a) de 1 à 90% en poids environ d'une source de chlore encapsulée ;
    (b) de 0,01 à 1,0% en poids environ d'un colorant ;
    (c) de 0,5 à 20% en poids environ d'une source d'acide ; et
    (d) une portion majeure d'un sel adjuvant.
  35. Procédé selon la revendication 34, dans lequel la source de chlore encapsulée comprend un composé chloroisocyanurate encapsulé.
  36. Procédé selon la revendication 34, dans lequel le chlore encapsulé comprend une source de particules de chlore, une première couche inorganique et une deuxième couche organique.
  37. Procédé selon la revendication 34, dans lequel le colorant comprend un colorant FD & C n° 40.
  38. Procédé selon la revendication 34, dans lequel le sel d'acide comprend le dihydrogénophosphate de potassium, l'hydrogénotartrate de sodium ou des mélanges de ceux-ci.
  39. Procédé selon la revendication 34, dans lequel le sel adjuvant comprend le sulfate de sodium.
  40. Procédé selon la revendication 34, dans lequel le pH de la solution d'assainissement aqueuse est ajusté à un pH inférieur à 7 et à un pH auquel plus de 80% environ des espèces oxydantes se présentent sous forme de HOCl et moins de 20% environ des espèces oxydantes se présentent sous forme d'OCl-1.
  41. Procédé selon la revendication 34, dans lequel la couleur du colorant est maintenue dans la solution d'assainissement aqueuse pendant une durée allant de 3 à 6 heures environ.
EP00915847A 1999-02-24 2000-02-23 Desinfectant hypochloreux a couleur stable et procedes associes Expired - Lifetime EP1155109B1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US257086 1981-04-24
US501876 1990-03-30
US25708699A 1999-02-24 1999-02-24
US09/501,876 US20030059483A1 (en) 1999-02-24 2000-02-10 Color stable hypochlorous sanitizer and methods
PCT/US2000/004595 WO2000050554A1 (fr) 1999-02-24 2000-02-23 Desinfectant hypochloreux a couleur stable et procedes associes

Publications (2)

Publication Number Publication Date
EP1155109A1 EP1155109A1 (fr) 2001-11-21
EP1155109B1 true EP1155109B1 (fr) 2006-04-26

Family

ID=26945792

Family Applications (1)

Application Number Title Priority Date Filing Date
EP00915847A Expired - Lifetime EP1155109B1 (fr) 1999-02-24 2000-02-23 Desinfectant hypochloreux a couleur stable et procedes associes

Country Status (9)

Country Link
EP (1) EP1155109B1 (fr)
JP (1) JP2002537405A (fr)
CN (1) CN1230510C (fr)
AU (1) AU763904B2 (fr)
BR (1) BR0008287A (fr)
CA (1) CA2363741A1 (fr)
DE (1) DE60027550T2 (fr)
MX (1) MXPA01008617A (fr)
WO (1) WO2000050554A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11610467B2 (en) 2020-10-08 2023-03-21 Ecolab Usa Inc. System and technique for detecting cleaning chemical usage to control cleaning efficacy

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2835702A1 (fr) * 2002-02-12 2003-08-15 Dominique Mercier Composition desinfectante caracterisee en ce qu'elle consiste de ou comprend un melange d'eau de javel et de monophosphate de sodium
US7875359B2 (en) 2005-01-13 2011-01-25 Akzo Nobel N.V. Opacifying polymers
US8048837B2 (en) 2005-01-13 2011-11-01 The Clorox Company Stable bleaches with coloring agents
US8642527B2 (en) 2007-06-18 2014-02-04 The Clorox Company Oxidizing bleach composition
GB2488838A (en) * 2011-03-11 2012-09-12 Biomimetics Health Ind Ltd A stable antimicrobial aqueous hypochlorous acid solution
CN103388257A (zh) * 2013-08-05 2013-11-13 天津成育庭科技有限公司 浅色重渍公共纺织品洗涤方法
CN109576088A (zh) * 2018-12-21 2019-04-05 上海应用技术大学 一种变色水垢清洗剂的制备方法
TWI727680B (zh) * 2020-02-27 2021-05-11 超水國際股份有限公司 次氯酸消毒劑及其生產方法
JP6871663B1 (ja) * 2020-05-27 2021-05-12 和日庵株式会社 次亜塩素酸水、次亜塩素酸水を調製するための組成物、及び次亜塩素酸水の判定用の試験紙
CA3173149A1 (fr) * 2021-04-27 2023-10-26 Kara NG Colorants a protection reversible et methodes d'utilisation

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE630391A (fr) * 1962-04-06
GB1049051A (en) * 1964-01-17 1966-11-23 Jeyes Group Ltd Improvements in and relating to cleaning preparations
DK536585A (da) * 1985-04-30 1986-10-31 Economics Lab Indkapslede halogene blegemidler samt fremgangsmaade til fremstillingog anvendelse heraf
AU2627388A (en) * 1987-11-28 1989-07-05 Fibre Treatments (Holdings) Limited A wiping product
US5089162A (en) * 1989-05-08 1992-02-18 Lever Brothers Company, Division Of Conopco, Inc. Cleaning compositions with bleach-stable colorant
US5358653A (en) * 1990-06-25 1994-10-25 Ecolab, Inc. Chlorinated solid rinse aid
GB9712680D0 (en) * 1997-06-18 1997-08-20 Reckitt & Colmann Prod Ltd Improvements in or relating to disinfecting materials
AU3907697A (en) * 1997-08-05 1999-03-01 Procter & Gamble Company, The Decolorizing compositions
ID26651A (id) * 1998-02-04 2001-01-25 Unilever Nv Komposisi pembersihan toilet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11610467B2 (en) 2020-10-08 2023-03-21 Ecolab Usa Inc. System and technique for detecting cleaning chemical usage to control cleaning efficacy
US12100285B2 (en) 2020-10-08 2024-09-24 Ecolab Usa Inc. System and technique for detecting cleaning chemical usage to control cleaning efficacy

Also Published As

Publication number Publication date
WO2000050554A1 (fr) 2000-08-31
BR0008287A (pt) 2001-11-06
AU3705100A (en) 2000-09-14
DE60027550D1 (de) 2006-06-01
DE60027550T2 (de) 2007-04-26
CA2363741A1 (fr) 2000-08-31
CN1230510C (zh) 2005-12-07
CN1341145A (zh) 2002-03-20
EP1155109A1 (fr) 2001-11-21
MXPA01008617A (es) 2002-07-30
WO2000050554B1 (fr) 2001-01-18
JP2002537405A (ja) 2002-11-05
AU763904B2 (en) 2003-08-07

Similar Documents

Publication Publication Date Title
US20030059483A1 (en) Color stable hypochlorous sanitizer and methods
US4452713A (en) Inhibition of the staining of porcelain surfaces by manganese
JP3566454B2 (ja) 製品の消毒および漂白方法およびそれらに用いられる組成物
US4049467A (en) Method and compositions for removal of hard surface manganese ion-derived discolorations
CN100487099C (zh) 增稠的抽水马桶清洁剂
US4512908A (en) Highly alkaline liquid warewashing emulsion stabilized by clay thickener
EP1155109B1 (fr) Desinfectant hypochloreux a couleur stable et procedes associes
HU218008B (hu) Ezüst korróziója ellen védő szerek (I) és ezeket tartalmazó gépi tisztítószerek
JPH09512040A (ja) ペルカルボン酸によるすすぎ方法
JP2008050410A (ja) 自動食器洗浄機用粒状洗浄剤組成物およびその製法、並びにその使用方法
JP2013528679A (ja) 器物洗浄用の高濃縮苛性ブロック
WO2000050554A9 (fr) Desinfectant hypochloreux a couleur stable et procedes associes
CA1148057A (fr) Methode et composition pour prevenir la formation de taches de manganese a la surface d'articles vitrifies
US20090082245A1 (en) Method for formulating a branded cleaning product
CA1148058A (fr) Methode et composition pour prevenir la formation de taches de manganese a la surface d'articles vitrifies
JP4335514B2 (ja) 自動洗浄機用粉粒状洗浄剤組成物
US20090099054A1 (en) Method for formulating a reduced phosphorus branded cleaning product or cleaning system
EP0018344B1 (fr) Procédé et composition pour inhiber l'encrassement des surfaces de porcelaine par le manganèse, et appareil doseur pour chasse d'eau utilisant ladite composition
NZ233357A (en) Automatic dishwashing detergent composition comprising a dual bleach system of a hypochlorite and a bromide compound
DE4338724A1 (de) Silberkorrosionsschutzmittel II
JP2983761B2 (ja) 着色液体洗浄漂白剤組成物
EP1799804B1 (fr) Composition de blanchiment aqueuse
JPH0827488A (ja) 液体硬表面洗浄剤組成物
EP3244733B1 (fr) Composition antimicrobienne pour le nettoyage d'une surface dure
CA1148056A (fr) Methode et composition pour prevenir la formation de taches de manganese a la surface d'articles vitrifies

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: 20010720

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

17Q First examination report despatched

Effective date: 20040402

RBV Designated contracting states (corrected)

Designated state(s): DE FR GB NL

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

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB NL

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 60027550

Country of ref document: DE

Date of ref document: 20060601

Kind code of ref document: P

ET Fr: translation filed
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

26N No opposition filed

Effective date: 20070129

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

Ref country code: FR

Payment date: 20070201

Year of fee payment: 8

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20081031

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

Ref country code: FR

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

Effective date: 20080229

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

Ref country code: NL

Payment date: 20190214

Year of fee payment: 20

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

Ref country code: DE

Payment date: 20190212

Year of fee payment: 20

Ref country code: GB

Payment date: 20190220

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 60027550

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MK

Effective date: 20200222

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20200222

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 EXPIRATION OF PROTECTION

Effective date: 20200222