EP0451924A2 - Enzym-stabilisierende Zusammensetzung und stabilisiertes Enzym enthaltende verstärkte Waschmittelzusammensetzungen - Google Patents

Enzym-stabilisierende Zusammensetzung und stabilisiertes Enzym enthaltende verstärkte Waschmittelzusammensetzungen Download PDF

Info

Publication number
EP0451924A2
EP0451924A2 EP91200871A EP91200871A EP0451924A2 EP 0451924 A2 EP0451924 A2 EP 0451924A2 EP 91200871 A EP91200871 A EP 91200871A EP 91200871 A EP91200871 A EP 91200871A EP 0451924 A2 EP0451924 A2 EP 0451924A2
Authority
EP
European Patent Office
Prior art keywords
enzyme
weight
composition
acid
detergent 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.)
Granted
Application number
EP91200871A
Other languages
English (en)
French (fr)
Other versions
EP0451924B1 (de
EP0451924A3 (en
Inventor
Hoai-Chau Cao
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.)
Colgate Palmolive Co
Original Assignee
Colgate Palmolive 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=24027097&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0451924(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of EP0451924A2 publication Critical patent/EP0451924A2/de
Publication of EP0451924A3 publication Critical patent/EP0451924A3/en
Application granted granted Critical
Publication of EP0451924B1 publication Critical patent/EP0451924B1/de
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38663—Stabilised liquid enzyme compositions

Definitions

  • This invention relates to stable, built, enzyme-containing liquid detergent compositions suitable for laundry or pre-soak formulations. More particularly, the invention relates to aqueous enzyme-containing liquid detergent compositions which contain one or more detergent builders and which are characterized by being physically stable, homogeneous liquid compositions, having improved enzyme stability. The invention also relates to the novel stabilized enzyme preparation useful a laundry additive, as well as to the novel enzyme stabilization system, per se.
  • the formulation of stabilized enzyme-containing liquid detergent compositions has been the focus of much attention in the prior art.
  • the desirability of incorporating enzymes into detergent compositions is primarily due to the effectiveness of proteolytic and amylolytic enzymes in decomposing proteinaceous and starch materials found on soiled fabrics, thereby facilitating the removal of stains, such as, gravy stains, blood stains, chocolate stains and the like during laundering.
  • enzymatic materials suitable for laundry compositions, particularly proteolytic enzymes are relatively expensive. Indeed, they generally are among the most expensive ingredients in a typical commercial liquid detergent composition, even though they are present in relatively minor amounts.
  • enzymes are known to be unstable in aqueous compositions.
  • liquid detergent compositions containing a builder In the case of liquid detergent compositions containing a builder, the problem of enzyme instability is particularly acute. Primarily this is because detergent builders have a destabilizing effect on enzymes, even in compositions containing enzyme stabilizers which are otherwise effective in unbuilt formulations. Moreover, the incorporation of a builder into a liquid detergent composition poses an additional problem, namely, the ability to form a stable single-phase composition; the solubility of sodium tripolyphosphate, for example, being relatively limited in aqueous compositions, and especially in the presence of anionic and nonionic detergents.
  • a polyacid capable of forming water-soluble Ca-complexes such as citric acid
  • calcium ion in an amount of from 0.5 to 15 millimoles per liter as an enzyme stabilizer.
  • U.S. Patent 4,287,082 to Tolfo, et al. discloses homogeneous enzyme-containing liquid detergents characterized by the presence of a C10-C16 saturated fatty acid, calcium ion and a C1-C3 short chain monocarboxylic acid or salt thereof.
  • U.S. Patent 4,318,818 to Letton, et al. also describes an enzyme composition which is stabilized by calcium ion and a short chain length carboxylic acid salt.
  • a polyacid may also be present in the compositions of Letton, et al. as well as those of Tolfo, et al.
  • an aqueous enzyme-containing liquid detergent composition containing an enzyme stabilizing mixture consisting of certain dicarboxylic acids and borax.
  • such dicarboxylic acid-borax mixtures in common with the aforementioned mixtures of glycerine and borax provide only a modest stabilizing effect in unbuilt liquid detergent compositions, especially under freeze-thaw conditions.
  • U.S. Patent 4,529,525 to Dormal, et al. discloses an unbuilt stabilized enzyme-containing liquid detergent composition
  • an unbuilt stabilized enzyme-containing liquid detergent composition comprising: (a) from about 5 to about 75%, by weight, of one or more non-soap detergent surface active agents selected from the group consisting of anionic, nonionic, cationic, ampholytic and zwitterionic detergent compounds; (b) from about 0.1 to about 20 millimoles of calcium ion per liter of composition; (c) from about 0.05 to about 5%, by weight, of an enzyme selected from the group consisting of proteases, amylases and mixtures thereof; (d) from about 0.1 to about 10%, by weight, of a stabilizing agent comprising (i) at least one water-soluble salt of a dicarboxylic acid represented by the formula (CH2)n(COOH)2 wherein n is an integer from 1 to 6; and/or (ii) at least one water-soluble salt of an unsatur
  • U.S. Patent 4,842,769 to Shulman, et al. discloses a stabilized fabric softening built, enzyme-containing liquid detergent composition comprising:
  • the enzyme stabilizer system includes 0.5 to 5% of a mixture of dibasic acid of 4 to 6 carbon atoms each, 1 to 3% of boric acid and 0.1 to 0.5% of a source of calcium ion.
  • the stabilizing power of this stabilization system is less efficient than the stabilization system according to this invention.
  • the present invention provides a built liquid detergent composition which contains, on a weight basis,
  • the built enzyme-containing liquid composition includes
  • laundering of stained and/or soiled materials is affected by contacting such materials with an aqueous solution of the above-defined liquid detergent compositions.
  • the described liquid detergent is a commercially acceptable heavy duty laundry detergent, capable of satisfactorily cleaning laundry items containing both oily and particulate soils. Additionally, the described compositions may be employed for the pre-treatment of badly soiled areas, such as collars and cuffs, of items to be laundered.
  • the three components of the enzyme stabilization system are typically separately added to the aqueous built laundry detergent composition during the manufacture of the detergent composition, it is also possible to separately formulate a stabilized dry or aqueous enzyme preparation which can be added as such during detergent manufacture or can be added directly by the end user to the washing machine or to soiled fabrics.
  • the three-component stabilization system can be separately prepared in either dry form, e.g. powder or granules or as an aqueous solution and added directly during the manufacture of the laundry detergent composition prior to the addition thereto of the enzyme(s).
  • the present invention also provides a stabilized enzyme preparation useful as a laundry additive containing either or both of protease and amylase enzyme, and an enzyme stabilizing effective amount of an enzyme stabilization system consisting essentially of (i) from about 0.25 to about 10 parts by weight of boric acid, boron oxide or alkali metal borate; (ii) from about 1 to about 3 parts by weight of an hydroxypolycarboxylic acid having 2 or 3 carboxylic acid groups and 1 to 4 hydroxyl groups and containing from 4 to 8 carbon atoms and (iii) a water-soluble calcium salt in an amount to provide from about 18 to about 50 millimoles calcium ion per liter.
  • the present invention also provides an enzyme stabilization system with the three components (i), (ii) and (iii) as defined immediately above.
  • the present invention is predicated upon the discovery of a three component enzyme stabilizing system as herein defined which provides an enzyme stabilizing effect to aqueous liquid detergent compositions superior to that which can be achieved with conventional enzyme stabilizers.
  • the enzyme stabilizing effect thus achieved reflects a synergy among the three components as most clearly manifested by the results in accelerated aging tests, including repetitive freeze-thaw cycles as described hereinafter.
  • the enzyme stabilizing system of the invention is a mixture of (i) a boron compound selected from among boric acid, boric oxide and an alkali metal borate, particularly sodium borate, especially sodium tetraborate, e.g. borax (Na2BrO7 ⁇ 10H2O), (ii) an hydroxypolycarboxylic acid having from 4 to 8 carbon atoms, preferably 4, 5 or 6 carbon atoms, two or three carboxyl (-COOH) groups and 1 to 4, preferably 2 or 3 hydroxyl (-OH) groups, and (iii) a water-soluble calcium salt capable of providing calcium (Ca++) ions in aqueous media.
  • a boron compound selected from among boric acid, boric oxide and an alkali metal borate, particularly sodium borate, especially sodium tetraborate, e.g. borax (Na2BrO7 ⁇ 10H2O), (ii) an hydroxypolycarboxylic acid having from 4 to 8 carbon
  • the boron compound (i) is boric acid or a compound capable of producing boric acid, such as boric oxide or a salt, such as sodium borate.
  • Borax is readily available and is preferred.
  • the boric acid compound is used in an amount of from about 0.25% to about 10%, preferably from about 0.5% to about 8%, more preferably from about 1% to about 5%, such as 2%, 3% or 4%, by weight, of the total detergent composition.
  • Citric acid is the preferred hydroxypolycarboxylic acid, especially in view of its ready availability and its contribution to improving the overall physical stability of the composition, i.e, prevent phase separation.
  • hydroxycarboxylic acids such as malic acid, tartaric acid, isocitric acid, tricarballylic acid, trihydroxyglutaric acid and mucic acid, may also be used.
  • Lactic acid which has only 3 carbon atoms, will also provide enzyme stabilization; however, replacing e.g. citric acid with an equal weight of lactic results in compositions which are physically unstable - i.e. undergo phase separation.
  • the acid is usually incorporated into the composition as the free acid (or hydrated free acid), but may also be added in the form of its salt, especially alkali metal salt. In fact, it is thought that under the preferred alkaline pH conditions for the detergent compositions, the hydroxypolycarboxylic acid will be present in its ionized (salt) state.
  • the hydroxypolycarboxylic acid is used in an amount of from about 1% to about 3%, preferably from about 1.2 to 2.6%, by weight of the total detergent composition.
  • the level of calcium ion as component (iii) in the detergent composition is from about 18 to about 50 millimoles, preferably from about 22 to about 36 millimoles, per liter of the composition.
  • Suitable water-soluble calcium salts which can be used as a source of calcium ion include both inorganic and organic salts, such as calcium chloride, calcium acetate and calcium formate. Calcium chloride is preferred. About 0.2% CaCl2 corresponds to about 18 millimoles Ca++ per liter.
  • a small amount of calcium ion generally from about 0.05 to about 0.4 millimole per liter, is often also present due to calcium in the enzyme preparation or water, but any such naturally present calcium ion will generally be insignificant to the added calcium ion.
  • the individual ingredients (i), (ii) and (iii) are usually separately added in any convenient order during the manufacture of the aqueous built laundry detergent compositions. However, it may also be convenient in some cases to separately prepare a stabilized enzyme preparation which can then be directly added to the other ingredients of the laundry detergent composition.
  • the stabilized enzyme composition may be formulated as a free flowing dry mix, such as powder or granules, containing up to about 20% by weight of water, or may be formulated as a concentrated aqueous solution.
  • aqueous stabilized enzyme preparation with or without any additional surface active agent, as required for stabilizing the composition can also be used directly to assist in the laundering process, for example, as a separate additive for use in combination with an enzyme-free laundry detergent composition.
  • the enzyme preparation may be added directly to the washing machine, before, after, or simultaneously with a separately prepared laundry detergent composition, or it may be used as a presoak by using it directly on soiled laundry.
  • the three components (i), (ii) and (iii) in this embodiment of the invention will generally comprise from about 5 to 75% of the total composition, preferably 10 to 60% of the total composition, the balance being the enzyme and aqueous carrier, usually water which may contain a small amount of surface active agent, such as the anionic, nonionic or amphoteric surface active agents to be described below, for example, up to about 20%, preferably up to about 10% of the stabilized aqueous enzyme composition.
  • aqueous carrier usually water which may contain a small amount of surface active agent, such as the anionic, nonionic or amphoteric surface active agents to be described below, for example, up to about 20%, preferably up to about 10% of the stabilized aqueous enzyme composition.
  • the three component stabilizing system may also be separately prepared without the enzyme and added as such to the remaining ingredients of the aqueous built laundry detergent composition at any time prior to the addition of the enzyme(s).
  • alkaline proteolytic enzymes suitable for the present compositions include the various commercial liquid enzyme preparations which have been adapted for use in detergent compositions. Enzyme preparations in powdered form are also useful although, as a general rule, less convenient for incorporation into the built liquid detergent compositions.
  • suitable liquid enzyme preparations include "Alcalase,” “Savinase,”, and “Esperase”, all trademarked products sold by Novo Industries, Copenhagen, Denmark, and "Maxatase,” “Maxacal,” and “AZ-Protease” sold by Gist-Brocades, Delft, The Netherlands.
  • alpha-amylase liquid enzyme preparations are those sold by Novo Industries and Gist-Brocades under the tradenames "Termamyl” and “Maxamyl,” respectively.
  • “Esperase” is particularly preferred for the present compositions because of its optimized activity at the higher pH values corresponding to the built detergent compositions.
  • Mixtures of proteolytic and amylase enzymes can and often are used to assist in removal of different types of stains.
  • the proteolytic enzyme and/or amylase enzyme will normally be present in the compositions in an effective amount in the range of from about 0.01% to about 5%, preferably from about 0.05% to about 2%, by weight of the composition.
  • the suitable amounts will generally provide from about 0.005 to about 0.1, more preferably from about 0.01 to about 0.07 Anson units per gram of composition, depending on the use to which the composition will be applied. Generally, lower levels of amylase are required.
  • Lipolytic, cellulytic and carbohydroxylytic enzymes are also commercially available may also be employed.
  • the preferred detergents for use in the present liquid compositions are the synthetic anionic detergent compounds, and particularly alkyl polyethoxy sulfate.
  • Other water soluble anionic detergent compound such as higher alkylbenzene sulfonates may also be present in the instant formulas, such as potassium salts and in some instances the ammonium or alkanolamine salts, however, it has been found that the sodium salt is highly preferred, which is also the case with respect to the alkyl polyethoxy sulfate detergent component.
  • the alkylbenzene sulfonate is one wherein the higher alkyl is of 12 to 15 carbon atoms, preferably 13 carbon atoms.
  • the alkyl polyethoxy sulfate which also may be referred to as a sulfated polyethoxylated higher linear alcohol or the sulfated condensation product of a higher fatty alcohol and ethylene oxide or polyethoxylene glycol, is one wherein the alkyl is of 10 to 18 carbon atoms, preferably 12 to 15 carbon atoms, e.g. about 13 carbon atoms, and which includes 3 to 11 ethylene oxide groups, preferably 3 to 7, more preferably 3 to 5 and most preferably 3, or about 3 ethylene oxide groups on average.
  • alkyl polyethoxy sulfate and alkylbenzene sulfonate are often advantageous and can be used at a ratio of alkylbenzene sulfonate to polyethoxy sulfate in the detergent mixture of from about 1:6 to 6:1 and most preferably from about 1:4 to 4:1, by weight. At ratios above 5:1, the physical stability of the product may be adversely affected.
  • anionic detergents such as fatty alcohol sulfates, paraffin sulfonates, olefin sulfonates, monoglyceride sulfates, sarcosinates and similarly functioning detergents, preferably as the alkali metal, e.g. sodium salts, can be present, sometimes in partial replacement of the previously mentioned synthetic organic detergents but usually, if present, in addition to such detergents.
  • the supplementing detergents will be sulfated or sulfonated products (usually as the sodium salts) and will contain long chain (e.g. 8 to 20 carbon atoms) linear or fatty alkyl groups.
  • nonionic and amphoteric materials like the Neodols ® sold by Shell Chemical Company, which are condensation products of ethylene oxide and higher fatty alcohols, e.g. Neodol ® 23-6.5, which is a condensation product of a higher fatty alcohol of about 12 to 13 carbon atoms with about 6.5 moles of ethylene oxide. Illustrations of the various detergents and classes of detergents mentioned may be found in the text Surface Active Agents , Vol. II, by Schwartz, Perry and Berch (Interscience Publishers, 1958), the descriptions of which are incorporated herein by reference.
  • the nonionic detergents also include the polyethylene oxide condensate of 1 mole of alkyl phenol containing in the alkyl group from about 6 to 12 carbon atoms in a straight or branched chain configuration with about 5 to 30 moles of ethylene oxide, for example, nonyl phenol condensed with 9 moles of ethylene oxide; dodecyl phenol condensed with 15 moles of ethylene oxide; and dinonyl phenol condensed with 15 moles of ethylene oxide.
  • Condensation products of the corresponding alkyl thiophenols with 5 to 30 moles of ethylene oxide are also suitable.
  • nonionic surfactants those of the ethoxylated and mixed ethoxylated propyloxylated fatty alcohol type are preferred.
  • preferred nonionic surfactants include the condensation product of coconut fatty alcohol with about 6 moles of ethylene oxide per mole of coconut fatty alcohol; the condensation product of tallow fatty alcohol with about 11 moles of ethylene oxide per mole of tallow fatty alcohol; the condensation product of a secondary fatty alcohol containing about 11-15 carbon atoms with about 9 moles of ethylene oxide per mole of fatty alcohol and condensation products of more or less branched primary alcohols, whose branching is predominantly 2-methyl, with from about 4 to 12 moles of ethylene oxide.
  • nonionics are represented by the commercially well-known class of nonionics which are the reaction product of a higher linear alcohol and a mixture of ethylene and propylene oxides, containing a mixed chain of ethylene oxide and propylene oxide, terminated by a hydroxyl group.
  • examples include the nonionics such as a C13-C15 fatty alcohol condensed with 7 moles propylene oxide and 4 moles ethylene oxide, a C13-C15 fatty alcohol condensed with 5 moles propylene oxide and 10 moles ethylene oxide, a C13-C15 fatty alcohol condensed with 6 moles ethylene oxide and 3 moles propylene oxide, etc.
  • the mixed ethylene oxide-propylene oxide fatty alcohol condensation products represented by the general formula RO(C3H6O) p (C2H4O) q H, wherein R is a hydrocarbyl group, such as straight or branched, primary or secondary aliphatic hydrocarbon, preferably alkyl or alkenyl, especially preferably alkyl, of from 8 to 20, preferably 10 to 18, especially preferably 12 to 18 carbon atoms, p is a number of from 2 to 8 on average, preferably 3 to 6, and q is a number of from 2 to 12 on average, preferably 4 to 10, can be advantageously used where low foaming characteristics are desired.
  • these surfactants have the advantage of low gelling temperatures.
  • Mixtures of two or more of the mixed ethylene oxide-propylene oxide fatty alcohol condensation product can be used as can mixtures of the mixed ethylene oxide-propylene oxide condensation products with any of the above alkoxylated nonionics, or mixtures of the ethoxylated nonionics can also be used.
  • Ampholytic detergents are also suitable for the invention.
  • Ampholytic detergents are well known in the art and many operable detergents of this class are disclosed by A. M. Schwartz, J.W. Perry and J. Berch in "Surface Active Agents and Detergents,” Interscience Publishers, New York, 1958, Vol. 2.
  • amphoteric detergents include: alkyl betaiminodipropionates, RN(C2H4COOM)2; alkyl beta-aminopropionates, RN(H)C2H4COOM; and long chain imidazole derivatives having the general formula: wherein in each of the above formulae, R is a hydrophobic hydrocarbyl group, preferably an aliphatic group, containing from about 8 to 20 carbon atoms, especially 10 to 18 carbon atoms, and M is a cation, e.g. alkali metal, ammonium salt, amine, alkanol amine, etc., to neutralize the charge of the anion.
  • R is a hydrophobic hydrocarbyl group, preferably an aliphatic group, containing from about 8 to 20 carbon atoms, especially 10 to 18 carbon atoms
  • M is a cation, e.g. alkali metal, ammonium salt, amine, alkanol amine, etc.
  • Specific operable amphoteric detergents include, for example, the disodium salt of undecylcycloimidiniumethoxyethionic acid-2-ethionic acid, dodecyl beta alanine, and the inner salt of 2-trimethylamino lauric acid.
  • amphoteric surfactants are the glycinate derivatives of the formula: wherein R is a hydrocarbyl group, prefferably aliphatic, of 8 to 20 carbon atoms, R1 is hydrogen or alkyl of 1 to 6 carbon atoms, preferably hydrogen, R2 is alkylene of 1 to 6 carbon atoms, preferably methylene, T is hydrogen or W, preferably W, W is R2COOM, M is hydrogen, alkali metal, alkaline earth metal, ammonium or substituted ammonium, such as lowre alkanolammonium, e.g., triethanol-ammonium, x is 2 to 3 and y is 2 to 4.
  • R is a hydrocarbyl group, prefferably aliphatic, of 8 to 20 carbon atoms
  • R1 is hydrogen or alkyl of 1 to 6 carbon atoms, preferably hydrogen
  • R2 is alkylene of 1 to 6 carbon atoms, preferably methylene
  • T is hydrogen or W, preferably W
  • a preferred amphoteric surfactant is of the formula wherein R is an aliphatic hydrocarbyl, preferably fatty alkyl or fatty alkylene, of 16 6o 18 carbon atoms, M is alkali metal, and y is 3 to 4. More preferably R is tallowalkyl (which is a mixture of stearyl, palmityl and oleyl in the proportions in which they occur in tallow), M is sodium and y is about 3.5, representing a mixture of about equal parts of the amphoteric surfactant wherein y is 3 and such amphoteric surfactant wherein y is 4.
  • AmpholakTM 7TX which is obtainable from Kenobel AB, a unit of Nobel Industries, Sweden.
  • the amount of the detergent active compound(s) will generally range from about 5% to about 75%, more usually from about 5% to about 30%, especially from about 8% to about 15%, by weight of the composition.
  • the preferred anionic surfactant is usually present in amounts of from about 1 to 25%, preferably from about 4 to 20%, especially preferably from about 5 to 15% by weight of the composition.
  • the nonionic surfactant when present, is usually contained in amounts of from about 1 to 10%, preferably from about 2 to 8%, by weight and the amphoteric, when present, may comprise from about 0.3 to 15%, preferably 1 to 10%, especially preferably from about 2 to 8% by weight, based on the total composition.
  • any of the conventional inorganic or organic water-soluble or water dispersible detergency builders can be used in the compositions of this invention.
  • the alkali metal polyphosphates and alkali metal carbonates or bicarbonates are preferred.
  • Sodium tripolyphosphate is especially preferred but other phosphate builders, such as tetrasodium pyrophosphate, tetrapotassium pyrophosphate, sodium metaphosphate, and the like, can also be used. Mixtures of sodium tripolyphosphate and sodium carbonate, as disclosed in U.S. Patent 4,842,769, incorporated herein by reference, may also be useful.
  • Suitable builders of the organic type include, for example, polycarboxylate builders, such as aminopolycarboxylates, for example, sodium and potassium ethylene-diamine tetraacetate; sodium and potassium nitrotriacetate; and the polyacetal polycarboxylates, such as those described, for example, in U.S. Patents 4,144,226 and 4,315,092.
  • Other organic builders of the polycarboxylate type include the water-soluble salts, especially sodium and potassium salts, of mellitic acid, citric acid, pyromellitic acid, benzene polycarboxylic acids, carboxymethyloxy succinic acid, cis-cyclohexane hexacarboxylic acid, and the like.
  • Citric acid salts e.g. sodium citrate
  • Citric acid salts is often a preferred builder in non-phosphate or low phosphate formulations, and may also be used in this capacity in the detergent-enzyme compositions of this invention, in addition to any citrate which may be used in the enzyme stabilizing system of this invention.
  • Polyphosphonate salts represent another useful class of detergency builders, for example, sodium and potassium salts of ethylene diphosphonic acid, ethane-1-hydroxy-1,1-diphosphonic acid, and ethane-1,1,2-triphosphonic acid.
  • Aminopolyphosphonate compounds are also useful builders and may also be advantageously used as sequestrants. Suitable examples include soluble salts, e.g. sodium or potassium salts, of diethylene triamine pentamethylene phosphonic acid, ethylene diamine tetramethylene phosphonic acid, and hexamethylenediamine tetramethylene phosphonic acid.
  • soluble salts e.g. sodium or potassium salts, of diethylene triamine pentamethylene phosphonic acid, ethylene diamine tetramethylene phosphonic acid, and hexamethylenediamine tetramethylene phosphonic acid.
  • compositions may also incorporate a water soluble acrylic polymer which function as viscosity stabilizers, and in some cases can act to enhance cleaning performance under actual use conditions and may also be useful as deflocculents.
  • a water soluble acrylic polymer which function as viscosity stabilizers, and in some cases can act to enhance cleaning performance under actual use conditions and may also be useful as deflocculents.
  • Such polymers include polyacrylic acid, polymethacrylic acid, acrylic acid-methacrylic acid copolymers, hydrolyzed polyacrylamide, hydrolyzed polymethacrylamide, hydrolyzed acrylamidemethacrylamide copolymers, hydrolyzed polyacrylonitrile, hydrolyzed polymethacrylonitrile, hydrolized acrylonitrilemethacrylonitrile copolymers, or mixtures thereof.
  • Water soluble salts or partial salts of these polymers such as the respective alkali metal (e.g.
  • the weight average molecular weight of the polymers is from about 500 to about 15,000 and is preferably within the range of from 750 to 10,000.
  • Preferred polymers include polyacrylic acid, the partial sodium salt of polyacrylic acid or sodium polyacrylate having weight average molecular weights within the range of 1,000 to 5,000 or 6,000. These polymers are commercially available, and methods for their preparation are well-known in the art.
  • polyacrylate solutions useful in the present cleaning compositions include the sodium polyacrylate solution, Colloid ® 207 (Colloids, Inc., Newark, N.J.); the polyacrylic acid solution, Aquatreat ® AR-602-A (Alco Chemical Corp., Chattanooga, Tenn); the polyacrylic acid solutions (50-65% solids) and the sodium polyacrylate powders (M.W. 2,100 and 6,000) and solutions (45% solids) available as the Goodrite ® K-700 series from B. F. Goodrich Co.; and the sodium- or partial sodium salts of polyacrylic acid solutions (M.W. 1000 to 4500) available as the Acrysol ® series from Rohm and Haas.
  • thickening agents include, for example, methyl cellulose, carboxymethylcellulose (CMC), starch, polyvinyl pyrrolidone (PVP), gelatin, colloidal silica, natural or synthetic clays and the like.
  • CMC carboxymethylcellulose
  • PVP polyvinyl pyrrolidone
  • colloidal silica natural or synthetic clays and the like.
  • the detergent builder may also include water insoluble-type, especially the aluminosilicate type, particularly the zeolites, such as Zeolite A, usually in the form of its crystalline hydrate, although amorphous zeolites may also be useful.
  • zeolites such as Zeolite A
  • the amount of detergent builder may range from about 5% to about 30%, especially from about 5% to about 25%, more preferably from about 10 to 20%, by weight, based on the total composition.
  • the polyacrylate When the polyacrylate is used it is usually present in only minor amounts, such as from about 0.05 to 3%, preferably from about 0.1 to 1%, by weight of the composition.
  • liquid detergent compositions of the invention may also be present in the liquid detergent compositions of the invention, for example, soil-suspending agents, hydrotropes, corrosion inhibitors, dyes, perfumes, silicates, optical brighteners, suds boosters, suds depressants, e.g. silicone antifoaming agents, germicides, e.g. quaternary ammonium salts, preservatives, e.g. quaternium 15, anti-tarnishing agents, opacifiers, fabric-softening agents, oxygen-liberating bleaches such as sodium perborate or percarbonate with or without bleach precursors, buffers and the like.
  • soil-suspending agents e.g. silicone antifoaming agents, germicides, e.g. quaternary ammonium salts, preservatives, e.g. quaternium 15, anti-tarnishing agents, opacifiers, fabric-softening agents, oxygen-liberating bleaches such as sodium perborate or percarbon
  • a preferred fabric-softening agent is a smectite clay, such as sodium and calcium montmorillonites, sodium saponites, and sodium hectorites.
  • the sodium and calcium bentonites which are colloidal clay containing montmorillonites, such as the swelling bentonites wherein the predominant cation is sodium or calcium, are preferred.
  • the Western or Wyoming bentonites are especially preferred.
  • the calcium clays often provide superior softening performance than the sodium clays.
  • the swelling capacity of bentonite is generally associated with its fabric softening properties.
  • the swelling capacity of sodium bentonite is in the range of 3 to 20 milliliters/gram, preferably 7 to 15 ml/gram, and its viscosity, at 6% concentration in water, is usually in the range of 3 to 30 centipoises, preferably 8 to 30 centipoises.
  • Preferred swelling bentonites are solid under the trademark HI-JEL by Georgia Kaolin Co. These materials are the same as bentonites which were formerly sold under the trademarks MINERAL COLLOID and THIXO-JEL. They are selectively mined and beneficiated bentonites, and those considered to be most useful are available as HI-JEL Nos. 1, 2, 3, etc., corresponding to THIXO-JEL's Nos. 1, 2, 3, and 4. Such materials have a maximum free moisture content (before addition to the liquid medium) of 4% to 8% and specific gravities of about 26.
  • the bentonite is preferably one which will pass through a 200 mesh U.S. Sieve Series sieve, and most preferably at least 90% of the particles will pass through a No. 325 sieve, so that the equivalent diameter of the bentonite may be considered to be less than 74 microns, and more preferably less than about 44 microns.
  • Typical chemical analyses of some bentonites that are useful for making the present liquid detergents show that they contain from 64.8 to 73.0% of SiO2, 14 to 18% of Al2O3, 1.6 to 2.7% of MgO, 1.3 to 3.1% of CaO, 2.3 to 3.4% of Fe2O3, 0.8 to 2.8% of Na2O and 0.4 to 7.0% of K2O.
  • the Western bentonites are preferred, it is also possible to utilize other bentonites, such as those which may be made by treating Italian or similar bentonites containing relatively small proportions of exchangeable monovalent metals (sodium and potassium) with alkaline materials, such as sodium carbonate or calcium chloride, to increase the cation exchange capacities of such products.
  • the Na2O content of the bentonite should be at least about 0.5%, preferably at least 1% and more preferably at least 2% so that the clay will be satisfactorily swelling, with good softening and dispersing properties in aqueous suspension.
  • Preferred swelling bentonites of the types described above are sold under the trade names Laviosa and Winkelmann, e.g. Laviosa AGB and Winkelmann G-13.
  • bentonites which are particularly useful in the present liquid detergent compositions because of their white or very light color include American Colloid Company's Polarite KB 325, a California bentonite, and Georgia Kaolin's GK 129, a Mexican bentonite.
  • the amount of the clay softening agent will usually be within the range of from about 5 to about 20% by weight, preferably from about 6 to 15% by weight, based on the total composition
  • Another optional, but often preferred additive, in minor amounts is a higher fatty acid, which may be saturated or unsaturated, and may contain from about 10 to about 22 carbon atoms, preferably from about 16 to 20 carbon atoms.
  • Oleic acid is especially preferred in amounts of from about 0.1 to about 5%, preferably from about 0.5 to 2.5%, by weight of the composition.
  • fatty acids function in the invention compositions as anti-foaming agents. They may be used alone for this function but are often used in combination with the polysiloxane (silicone) anti-foaming agents.
  • the silicone anti-foaming agents will generally be present in minor amounts compared to the fatty acid. Suitable ratios (by weight) of the fatty acid anti-foaming agent to silicone anti-foaming agent may range from about 100:1 to 1:10, preferably 50:1 to 1:1, especially 30:1 to 2:1.
  • the liquid carrier for the liquid compositions of this invention is preferably water alone but an aqueous carrier containing minor amounts of a lower alcohol, such as ethanol or isopropanol, may also be used in some cases.
  • a lower alcohol such as ethanol or isopropanol
  • water levels may be up to about 70% by weight of the composition, for example, from about 20 to about 70%, preferably from about 30% to 60%, by weight.
  • the water may be deionized, but usually tap water is sufficient.
  • the viscosity of the present liquid detergent is normally in the range of about 1000 to 10,000 centipoises, preferably 2000-7000 centipoises, but products of other suitable viscosities may also be useful. At the viscosities mentioned, the liquid detergent is pourable, stable, nonseparating and uniform.
  • the pH of the liquid detergent suspension usually in the range of 7 to 11.5, preferably 8 to 10.5, appears to help to maintain product stability and pourability.
  • pH modifiers such as water soluble bases, e.g. caustic, amines, or ammonia, or acids, preferably mineral acids, e.g. HCl, will be added to obtain the desired pH level.
  • the ingredients can often be added in any desired order usually the enzyme will be the last added ingredient and will always follow the addition of the enzyme stabilizing additives.
  • a portion of the aqueous medium may be added to a mixing vessel and the surfactant components may be mixed therewith in any suitable order, such as anionic, nonionic and amphoteric detergents, followed by higher fatty acid and hydroxypolycarboxylic acid and neutralizing agent, such as sodium hydroxide solution. Then sodium tripolyphosphate and/or other builders may be added, followed by polyacrylate, enzyme and boric acid and calcium ion source.
  • Bentonite may be pre-mixed with another portion of the water or may be added directly to the composition, sometimes with additional water, after which the balance of the water, brightener, dye and perfume may be admixed.
  • other components of the detergent composition may be added to the mixer at appropriate times and the various orders of addition may be modified to make them appropriate to the types of products being made and to the types of equipment being used.
  • premixture of the calcium compound with some or all of the surface active compounds and with some or all of the hydroxypolycarboxylic acid.
  • the premix is prepared as a homogeneous aqueous mixture wherein the aqueous media (e.g. water) may be added as such or as a carrier for one of the other ingredients in the premix.
  • Anti-foaming agent may be included in the premix or in the main batch or both.
  • Thickening or viscosity modifiers and clay softener are preferably added to the main mixing batch, the viscosity modifiers generally being added at or near the beginning of the mixing sequence and clay added near the end of the mixing sequence before or after the premix.
  • a convenient order for addition of the ingredients is water, thickener, coloring agents and/or brighteners, borax and builder followed by the clay and premix and anti-foaming agent.
  • Final pH adjustment is usually made right before the enzyme component(s). The precise order of addition will depend on the specific ingredients, type of mixing apparatus and desired characteristics in the final product.
  • a liquid enzyme containing composition is prepared by first thoroughly mixing the following ingredients in the recited order until each ingredient is completely dissolved or uniformly dispersed to form a premix.
  • the enzyme stabilization system of borax/citric acid/calcium chloride is present at a mixing ratio of 3/2/0.4.
  • the enzyme stability is measured after being stored for four weeks at each of the following temperatures: 4°C, room temperature (20°C), 35°C and 43°C. The results are shown in Table 1. Also shown in Table 1 is the enzyme stability of the same composition except that the enzyme stabilization system (CaCl2, borax and citric acid) is omitted.
  • the enzyme stabilization system CaCl2, borax and citric acid
  • composition shown below is prepared similarly to the composition of Example 1
  • composition is subjected to an accelerated aging test ("freeze and thaw”) to predict the stability of enzyme activity under long term storage conditions.
  • the accelerated aging test is carried out in an automatic computer controlled double boiler. During each test cycle, the temperature is first decreased at 1°C/min. to 28°F (-2°C) and maintained at this temperature for 2 hours, then the temperature is increased at 1°C/min. to 122°F (50°C), and maintained at this elevated temperature for 2 hours. After 8, 24, 40, 72 and 80 cycles, the remaining enzyme activity is measured. The results are shown in Table 1. For comparison, the same test is run on compositions identical to that of example 1 but in which the amounts of borax, CaCl2 or citric acid are varied as also shown in Table 1 along with the results of the accelerated aging tests on these comparative compositions. As a further comparison, citric acid in the above example is replaced by an equal weight of Sokolan ® DCS, a mixture of succinic acid, glutaric acid and adipic acid (1:1.6:1). The results are also shown in Table 2.
  • Example 2 and the Sokolan R DCS control are also compared for long term storage (aging) characteristics by measuring the remaining enzyme activity (as a percent of the original activity) at 4°C, room temperature, 35°C and 43°C.
  • the enzyme stability in terms of remaining activity (percent of original activity) is measured at the end of 2 weeks, 4 weeks and 8 weeks at each temperature. The results are shown in Table 3.
  • composition shown above is prepared by the following procedure: 30.0 parts of deionized water at 40°F. are added to a suitable mixing apparatus such as a vertical cylindrical tank equipped with a stirrer. With the stirrer adjusted for medium agitation, a mixture consisting of 2.0 parts anhydrous soda ash, 2.0 parts sodium sesquicarbonate, and 0.2 parts sodium carboxymethyl cellulose is incorporated into the water. The stirrer speed is then increased to maximum agitation and a mixture comprised of 11.0 parts pentasodium tripolyphosphate and 12.0 parts bentonite is slowly added to the mixing apparatus over a period of 10-15 minutes to form an off-white suspension.
  • a suitable mixing apparatus such as a vertical cylindrical tank equipped with a stirrer. With the stirrer adjusted for medium agitation, a mixture consisting of 2.0 parts anhydrous soda ash, 2.0 parts sodium sesquicarbonate, and 0.2 parts sodium carboxymethyl cellulose is incorporated into the water. The stirrer speed is then increased to maximum agitation and a mixture
  • the agitation speed is then decreased to a slow/medium setting while 8.64 parts of high AI (about 55%) LTBS slurry is added. Thereafter the optical brightener/color solution is added consisting of 0.3 parts Tinopal LMS-X (CIBA-GEIGY), 0.909 parts colorant, and 4.02 parts deionized water. Once a uniform blueish green colored solution is obtained, 0.4 parts of perfume is added to the mixture under agitation. This is followed by the slow addition of 0.6 parts CaC12 and 2.5 parts borax as a two component slurry. Stirring is continued until the mixture is uniform in appearance and then 2.0 parts of citric acid and 9.0 parts water are slowly added.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP91200871A 1990-04-13 1991-04-12 Enzym-stabilisierende Zusammensetzung und deren Verwendung in stabilisierten Enzym enthaltenden verstärkten Waschmittelzusammensetzungen Revoked EP0451924B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US50954990A 1990-04-13 1990-04-13
US509549 1990-04-13

Publications (3)

Publication Number Publication Date
EP0451924A2 true EP0451924A2 (de) 1991-10-16
EP0451924A3 EP0451924A3 (en) 1992-03-11
EP0451924B1 EP0451924B1 (de) 1999-02-10

Family

ID=24027097

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91200871A Revoked EP0451924B1 (de) 1990-04-13 1991-04-12 Enzym-stabilisierende Zusammensetzung und deren Verwendung in stabilisierten Enzym enthaltenden verstärkten Waschmittelzusammensetzungen

Country Status (19)

Country Link
EP (1) EP0451924B1 (de)
AT (1) ATE176682T1 (de)
AU (1) AU651090B2 (de)
BR (1) BR9101486A (de)
CA (1) CA2040202A1 (de)
DE (1) DE69130880D1 (de)
DK (1) DK0451924T3 (de)
ES (1) ES2130131T3 (de)
FI (1) FI911800A (de)
GR (1) GR1001040B (de)
HK (1) HK1014026A1 (de)
IE (1) IE911245A1 (de)
MX (1) MX173751B (de)
MY (1) MY105503A (de)
NO (1) NO911448L (de)
NZ (1) NZ237570A (de)
PT (1) PT97325A (de)
TR (1) TR25788A (de)
ZA (1) ZA912598B (de)

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0580245A2 (de) * 1992-07-20 1994-01-26 Colgate-Palmolive Company Stabilisierte, wässrig-flüssige, verstärkte, Weichmacher enthaltende Waschmittelzusammensetzung
EP0583420B1 (de) * 1991-04-30 1996-03-27 The Procter & Gamble Company Gerüstsubstanzhaltige flüssigwaschmittel mit borsäure-polyolkomplex zur ptoteolytischen enzyminhibierung
WO1996021716A1 (en) * 1995-01-09 1996-07-18 Novo Nordisk A/S Stabilization of liquid enzyme compositions
US5904736A (en) * 1995-04-28 1999-05-18 Henkel Kommanditgesellschaft Auf Aktien Cellulase-containing washing agents
US6153576A (en) * 1996-02-16 2000-11-28 Henkel Kommanditgesellschaft Auf Aktien Transition-metal complexes used as activators for peroxy compounds
WO2002002727A1 (en) * 2000-06-29 2002-01-10 Ecolab Inc. Stable liquid enzyme compositions with enhanced activity
WO2002024851A1 (en) * 2000-09-20 2002-03-28 Reckitt Benckiser Inc. Aqueous compositions comprising protease and/or amylase
US6537958B1 (en) 1999-11-10 2003-03-25 The Procter & Gamble Company Bleaching compositions
EP1585817A2 (de) * 2002-02-20 2005-10-19 The General Hospital Corporation Konjugate mit biologisch abbaubarem polymer und verwendung dafür
DE102007011236A1 (de) 2007-03-06 2008-09-11 Henkel Ag & Co. Kgaa Carboxylgruppen tragende Benzophenon-oderBenzoesäureanilid-Derivate als Enzymstabilisatoren
DE102007041754A1 (de) 2007-09-04 2009-03-05 Henkel Ag & Co. Kgaa Polycyclische Verbindungen als Enzymstabilisatoren
DE102008010429A1 (de) 2008-02-21 2009-08-27 Henkel Ag & Co. Kgaa Harnstoff-Derivate als Enzymstabilisatoren
DE102008014760A1 (de) 2008-03-18 2009-09-24 Henkel Ag & Co. Kgaa Imidazolium-Salze als Enzymstabilisatoren
US7795199B2 (en) 2000-06-29 2010-09-14 Ecolab Inc. Stable antimicrobial compositions including spore, bacteria, fungi, and/or enzyme
EP2430195A2 (de) * 2009-05-11 2012-03-21 Biomatrica, INC. Zusammensetzungen und verfahren zur lagerung biologischer proben
DE102014218507A1 (de) 2014-09-16 2016-03-17 Henkel Ag & Co. Kgaa Spinnenseidenproteine als Enzymstabilisatoren
US9725703B2 (en) 2012-12-20 2017-08-08 Biomatrica, Inc. Formulations and methods for stabilizing PCR reagents
US9845489B2 (en) 2010-07-26 2017-12-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA and proteins in saliva and other biological samples during shipping and storage at ambient temperatures
US9999217B2 (en) 2010-07-26 2018-06-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA, and proteins in blood and other biological samples during shipping and storage at ambient temperatures
US10064404B2 (en) 2014-06-10 2018-09-04 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
US10568317B2 (en) 2015-12-08 2020-02-25 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
US12121022B2 (en) 2023-05-26 2024-10-22 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4037764A1 (de) * 1990-11-28 1992-06-04 Behringwerke Ag Waschloesung fuer festphasen-immunometrische verfahren, die stabilisatoren fuer das markierungssystem enthaelt und ihre verwendung
CA2560513A1 (en) 2004-04-08 2005-12-01 Biomatrica, Inc. Integration of sample storage and sample management for life science
US7723281B1 (en) 2009-01-20 2010-05-25 Ecolab Inc. Stable aqueous antimicrobial enzyme compositions comprising a tertiary amine antimicrobial
US7964548B2 (en) 2009-01-20 2011-06-21 Ecolab Usa Inc. Stable aqueous antimicrobial enzyme compositions
US9133424B2 (en) 2011-12-16 2015-09-15 Ecolab Usa Inc. Stabilization and activation of protease for use at high temperature

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2343805A1 (fr) * 1976-03-08 1977-10-07 Procter & Gamble Europ Composition detergente liquide contenant une enzyme
EP0199405A2 (de) * 1985-04-15 1986-10-29 The Procter & Gamble Company Flüssige Reinigungsmittel mit einer oberflächenaktiven Verbindung, einem proteolytischen Enzym und Borsäure
GB2178055A (en) * 1985-07-26 1987-02-04 Colgate Palmolive Co Stabilized built liquid detergent composition containing enzymes
FR2606028A1 (fr) * 1986-10-31 1988-05-06 Colgate Palmolive Co Systeme a enzyme stabilisee, procede pour le preparer, compositions detergentes le contenant et leurs procedes d'utilisation pour nettoyer des tissus salis

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2343805A1 (fr) * 1976-03-08 1977-10-07 Procter & Gamble Europ Composition detergente liquide contenant une enzyme
EP0199405A2 (de) * 1985-04-15 1986-10-29 The Procter & Gamble Company Flüssige Reinigungsmittel mit einer oberflächenaktiven Verbindung, einem proteolytischen Enzym und Borsäure
GB2178055A (en) * 1985-07-26 1987-02-04 Colgate Palmolive Co Stabilized built liquid detergent composition containing enzymes
FR2606028A1 (fr) * 1986-10-31 1988-05-06 Colgate Palmolive Co Systeme a enzyme stabilisee, procede pour le preparer, compositions detergentes le contenant et leurs procedes d'utilisation pour nettoyer des tissus salis

Cited By (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0583420B1 (de) * 1991-04-30 1996-03-27 The Procter & Gamble Company Gerüstsubstanzhaltige flüssigwaschmittel mit borsäure-polyolkomplex zur ptoteolytischen enzyminhibierung
EP0580245A3 (en) * 1992-07-20 1996-05-15 Colgate Palmolive Co Stabilized built aqueous liquid softergent compositions
TR28471A (tr) * 1992-07-20 1996-07-24 Colgate Palmolive Co Stabilize, kurulmus suda sivi softerjan bilesimleri.
EP0580245A2 (de) * 1992-07-20 1994-01-26 Colgate-Palmolive Company Stabilisierte, wässrig-flüssige, verstärkte, Weichmacher enthaltende Waschmittelzusammensetzung
WO1996021716A1 (en) * 1995-01-09 1996-07-18 Novo Nordisk A/S Stabilization of liquid enzyme compositions
US5904736A (en) * 1995-04-28 1999-05-18 Henkel Kommanditgesellschaft Auf Aktien Cellulase-containing washing agents
US6153576A (en) * 1996-02-16 2000-11-28 Henkel Kommanditgesellschaft Auf Aktien Transition-metal complexes used as activators for peroxy compounds
US6537958B1 (en) 1999-11-10 2003-03-25 The Procter & Gamble Company Bleaching compositions
US6624132B1 (en) 2000-06-29 2003-09-23 Ecolab Inc. Stable liquid enzyme compositions with enhanced activity
US7553806B2 (en) 2000-06-29 2009-06-30 Ecolab Inc. Stable liquid enzyme compositions with enhanced activity
US8211849B2 (en) 2000-06-29 2012-07-03 Ecolabb USA Inc. Stable antimicrobial compositions including spore, bacteria, fungi and/or enzyme
US7951767B2 (en) 2000-06-29 2011-05-31 Ecolab Usa Inc. Stable antimicrobial compositions including spore, bacteria, fungi and/or enzyme
US7795199B2 (en) 2000-06-29 2010-09-14 Ecolab Inc. Stable antimicrobial compositions including spore, bacteria, fungi, and/or enzyme
WO2002002727A1 (en) * 2000-06-29 2002-01-10 Ecolab Inc. Stable liquid enzyme compositions with enhanced activity
WO2002024851A1 (en) * 2000-09-20 2002-03-28 Reckitt Benckiser Inc. Aqueous compositions comprising protease and/or amylase
US7119054B2 (en) 2000-09-20 2006-10-10 Reckitt Benckiser Inc Aqueous compositions comprising protease and/or amylase
EP1585817A4 (de) * 2002-02-20 2005-12-28 Gen Hospital Corp Konjugate mit biologisch abbaubarem polymer und verwendung dafür
US7785618B2 (en) 2002-02-20 2010-08-31 Elmaleh David R Conjugates comprising a biodegradable polymer and uses therefor
EP1585817A2 (de) * 2002-02-20 2005-10-19 The General Hospital Corporation Konjugate mit biologisch abbaubarem polymer und verwendung dafür
DE102007011236A1 (de) 2007-03-06 2008-09-11 Henkel Ag & Co. Kgaa Carboxylgruppen tragende Benzophenon-oderBenzoesäureanilid-Derivate als Enzymstabilisatoren
DE102007041754A1 (de) 2007-09-04 2009-03-05 Henkel Ag & Co. Kgaa Polycyclische Verbindungen als Enzymstabilisatoren
DE102008010429A1 (de) 2008-02-21 2009-08-27 Henkel Ag & Co. Kgaa Harnstoff-Derivate als Enzymstabilisatoren
DE102008014760A1 (de) 2008-03-18 2009-09-24 Henkel Ag & Co. Kgaa Imidazolium-Salze als Enzymstabilisatoren
EP2430195A4 (de) * 2009-05-11 2014-02-19 Biomatrica Inc Zusammensetzungen und verfahren zur lagerung biologischer proben
EP2430195A2 (de) * 2009-05-11 2012-03-21 Biomatrica, INC. Zusammensetzungen und verfahren zur lagerung biologischer proben
US9999217B2 (en) 2010-07-26 2018-06-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA, and proteins in blood and other biological samples during shipping and storage at ambient temperatures
US9845489B2 (en) 2010-07-26 2017-12-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA and proteins in saliva and other biological samples during shipping and storage at ambient temperatures
US9725703B2 (en) 2012-12-20 2017-08-08 Biomatrica, Inc. Formulations and methods for stabilizing PCR reagents
US10064404B2 (en) 2014-06-10 2018-09-04 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
US10772319B2 (en) 2014-06-10 2020-09-15 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
US11672247B2 (en) 2014-06-10 2023-06-13 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures
DE102014218507A1 (de) 2014-09-16 2016-03-17 Henkel Ag & Co. Kgaa Spinnenseidenproteine als Enzymstabilisatoren
US10568317B2 (en) 2015-12-08 2020-02-25 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
US11116205B2 (en) 2015-12-08 2021-09-14 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
US12089588B2 (en) 2015-12-08 2024-09-17 Biomatrica, Inc. Reduction of erythrocyte sedimentation rate
US12121022B2 (en) 2023-05-26 2024-10-22 Biomatrica, Inc. Stabilization of thrombocytes at ambient temperatures

Also Published As

Publication number Publication date
CA2040202A1 (en) 1991-10-14
ZA912598B (en) 1992-12-30
FI911800A0 (fi) 1991-04-12
NO911448L (no) 1991-10-14
IE911245A1 (en) 1991-10-23
HK1014026A1 (en) 1999-09-17
PT97325A (pt) 1992-01-31
DK0451924T3 (da) 1999-09-20
MY105503A (en) 1994-10-31
GR1001040B (el) 1993-03-31
EP0451924B1 (de) 1999-02-10
ES2130131T3 (es) 1999-07-01
AU7400791A (en) 1991-10-17
NZ237570A (en) 1993-09-27
TR25788A (tr) 1993-09-01
AU651090B2 (en) 1994-07-14
MX173751B (es) 1994-03-25
FI911800A (fi) 1991-10-14
GR910100154A (en) 1992-07-30
DE69130880D1 (de) 1999-03-25
NO911448D0 (no) 1991-04-12
BR9101486A (pt) 1991-12-03
ATE176682T1 (de) 1999-02-15
EP0451924A3 (en) 1992-03-11

Similar Documents

Publication Publication Date Title
US5221495A (en) Enzyme stabilizing composition and stabilized enzyme containing built detergent compositions
EP0451924B1 (de) Enzym-stabilisierende Zusammensetzung und deren Verwendung in stabilisierten Enzym enthaltenden verstärkten Waschmittelzusammensetzungen
US5364553A (en) Stabilized built aqueous liquid softergent compositions
US4842758A (en) Stabilized enzyme system for use in aqueous liquid built detergent compositions
AU669900B2 (en) Stabilized built aqueous liquid softergent compositions
USH1776H (en) Enzyme-containing heavy duty liquid detergent
US5587356A (en) Thickened, highly aqueous, cost effective liquid detergent compositions
US5039446A (en) Liquid detergent with stabilized enzyme
US4900475A (en) Stabilized built liquid detergent composition containing enzyme
FI88726C (fi) Mjukgoerande tvaettmedelskomposition innehaollande amidmjukgoeringsmedel
US4842769A (en) Stabilized fabric softening built detergent composition containing enzymes
US5500151A (en) Heavy duty fabric softening laundry detergent composition
GB2144764A (en) Liquid detergent compositions
GB2168376A (en) Stabilized enzyme-containing detergent compositions
JPS6116796B2 (de)
CA1109757A (en) Low phosphate laundry detergent compositions
CA1297440C (en) Fabric softening liquid detergent
AU618036B2 (en) Machine dishwashing compositions
JP2749415B2 (ja) 酵素と酵素安定化系を含む液体洗剤組成物
JP3810854B2 (ja) 高密度粉末洗剤組成物
US6025316A (en) Detergent composition having improved cleaning power
GB2178054A (en) Stabilized built liquid detergent composition containing enzymes
US5565135A (en) Highly aqueous, cost effective liquid detergent compositions
US5948745A (en) Detergent composition having improved cleaning power
GB1577140A (en) Liquid detergent compositions

Legal Events

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

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH DE DK ES FR GB IT LI LU NL SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH DE DK ES FR GB IT LI LU NL SE

17P Request for examination filed

Effective date: 19920909

17Q First examination report despatched

Effective date: 19950720

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE DK ES FR GB IT LI LU NL SE

REF Corresponds to:

Ref document number: 176682

Country of ref document: AT

Date of ref document: 19990215

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 69130880

Country of ref document: DE

Date of ref document: 19990325

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: 19990412

ITF It: translation for a ep patent filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

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

Effective date: 19990511

ET Fr: translation filed
REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: E. BLUM & CO. PATENTANWAELTE

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2130131

Country of ref document: ES

Kind code of ref document: T3

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

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

Free format text: ORIGINAL CODE: EPIDOS OBSO

26 Opposition filed

Opponent name: UNILEVER N.V.

Effective date: 19991109

NLR1 Nl: opposition has been filed with the epo

Opponent name: UNILEVER N.V.

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

Ref country code: GB

Payment date: 20000306

Year of fee payment: 10

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

Ref country code: NL

Payment date: 20000320

Year of fee payment: 10

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

Ref country code: ES

Payment date: 20000411

Year of fee payment: 10

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

Free format text: ORIGINAL CODE: EPIDOS OBSO

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

Ref country code: DK

Payment date: 20000427

Year of fee payment: 10

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

Ref country code: SE

Payment date: 20000428

Year of fee payment: 10

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

Ref country code: AT

Payment date: 20000430

Year of fee payment: 10

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

Ref country code: BE

Payment date: 20000512

Year of fee payment: 10

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

Ref country code: CH

Payment date: 20000621

Year of fee payment: 10

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

Ref country code: GB

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

Effective date: 20010412

Ref country code: DK

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

Effective date: 20010412

Ref country code: AT

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

Effective date: 20010412

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

Ref country code: SE

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

Effective date: 20010413

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: 20010414

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 NON-PAYMENT OF DUE FEES

Effective date: 20010430

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

Ref country code: LI

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

Effective date: 20010511

Ref country code: CH

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

Effective date: 20010511

BERE Be: lapsed

Owner name: COLGATE-PALMOLIVE CY (A DELAWARE CORP.)

Effective date: 20010430

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

Ref country code: NL

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

Effective date: 20011101

PLBO Opposition rejected

Free format text: ORIGINAL CODE: EPIDOS REJO

EUG Se: european patent has lapsed

Ref document number: 91200871.1

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

Effective date: 20010412

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

APAE Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOS REFNO

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Effective date: 20011101

RTI2 Title (correction)

Free format text: ENZYME STABILIZING COMPOSITION AND THE USE THEREOF IN STABILIZED ENZYME CONTAINING BUILT DETERGENT COMPOSITIONS

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

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

Ref country code: FR

Payment date: 20020404

Year of fee payment: 12

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20030203

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: 20031231

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

APBU Appeal procedure closed

Free format text: ORIGINAL CODE: EPIDOSNNOA9O

RDAF Communication despatched that patent is revoked

Free format text: ORIGINAL CODE: EPIDOSNREV1

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

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

Free format text: STATUS: PATENT REVOKED

27W Patent revoked

Effective date: 20040324

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO