EP0462829A2 - Composition détergente pour lave-vaisselle automatique - Google Patents

Composition détergente pour lave-vaisselle automatique Download PDF

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Publication number
EP0462829A2
EP0462829A2 EP91305574A EP91305574A EP0462829A2 EP 0462829 A2 EP0462829 A2 EP 0462829A2 EP 91305574 A EP91305574 A EP 91305574A EP 91305574 A EP91305574 A EP 91305574A EP 0462829 A2 EP0462829 A2 EP 0462829A2
Authority
EP
European Patent Office
Prior art keywords
percent
weight
composition
copolymer
detergent
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.)
Withdrawn
Application number
EP91305574A
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German (de)
English (en)
Other versions
EP0462829A3 (en
Inventor
Charles Elwood Jones
George Max Lein
Andrea Claudette Keenan
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas 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
Application filed by Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of EP0462829A2 publication Critical patent/EP0462829A2/fr
Publication of EP0462829A3 publication Critical patent/EP0462829A3/en
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and 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
    • C11D9/00—Compositions of detergents based essentially on soap
    • C11D9/04—Compositions of detergents based essentially on soap containing compounding ingredients other than soaps

Definitions

  • the present invention is concerned with chlorine-free machine dishwashing detergent compositions which provide cleaning as effective as conventional chlorine-containing machine dishwashing compositions. More specifically, the present invention is concerned with dishwashing detergent compositions containing copolymers formed from maleic acid, maleic anhydride, or salts thereof, and a copolymerizable hydrophobic monomer, oligomer or polymer, containing from 4 to 20 carbon atoms. In one embodiment of the invention the machine dishwashing detergent contains low levels of, or no, phosphate.
  • Conventional machine dishwashing detergents generally contain an available chlorine releasing agent and a polyphosphate builder as critical components.
  • the chlorine agent such as 2 to 3% sodium dichloroisocyanurate, has generally been found to be necessary to achieve spot-free glassware.
  • the polyphosphate typically sodium tripolyphosphate, seemed vitally important to provide adequate soil removal, inhibit soil redeposition and prevent hard water salt deposits on glassware and other utensils.
  • the presence of a low-foaming surfactant is desirable because it can add significantly to the performance of the detergent by providing increased cleaning action and preventing soil redeposition. Even more importantly, when soil loads are high, some low-foam surfactants will defoam the protein food soil stabilized foam which markedly reduces the mechanical efficiency of the wash spray.
  • the reactions of oxidizing chlorine agent and the surfactant will be evidenced by an increased rate of loss of available chlorine and a gradual loss of surfactant performance, particularly in food soil defoaming capability.
  • U.S.-A-3,764,559 teaches the use of detergent compositions containing maleic anhydride polymers as a means to eliminate phosphates.
  • the polymers used in this patent are maleic anhydride copolymerized with vinyl acetate, utilized at a broad level of 5% to 65%, and a more preferred range of 20% to 50%, by weight of the copolymer.
  • U.S.-A-4,102,799 teaches the use of detergents essentially free of inorganic phosphates.
  • the detergents were shown to have improved effects on overglaze through the use of citrate substitution.
  • these detergents also contain organic phosphorus compounds in the form of phosphonates, so the compositions are not truly phosphorus free.
  • the detergent compositions of U.S.-A- 4,102,799 contain from about 0.5 to 5 percent by weight of a bleaching agent.
  • U.S.-A-4,182,684 teaches phosphate-free machine dishwashing detergent compositions by using from 5 to 90 percent by weight of a polymeric compound.
  • the detergent composition disclosed in U.S.-A-4,182,684 also contains a chlorine-containing compound, providing from 0.5 to 2 percent by weight available chlorine.
  • EP-B-0,132,792 teaches certain cleaning compositions for washing dishes in automatic dishwashers.
  • the compositions contain from 1 to 8 weight percent of a polycarboxylic acid having molecular weight of 12,000 to 40,000.
  • the detergent contains alkaline surfactants and standard additives such as bleaching agents, biocides, perfumes, foaming-inhibitors, and/or solubilizers.
  • the polymer can be polyacrylic or polymethacrylic acid or polymers of maleic acid or fumaric acid and ethylene or propylene.
  • DE-A-3627773 teaches a phosphate-free detergent composition utilizing a crystalline alkali layered silicate with a polymeric material.
  • the composition also makes use of a defoaming surfactant and an available chlorine source.
  • GB-A-2203163 teaches the use of a polyacrylic acid and a polyhydroxy acrylic acid in a liquid dishwashing composition.
  • this dishwashing detergent composition also requires the use of 3 to 15% by weight sodium hypochlorite and 0.4 to 6 percent by weight of a chlorine-resistant phosphonate or organic phosphate.
  • phosphate-free detergent compositions which are liquids or pastes, such as CA-A-1,158,522, GB-A-2,210,055 and CA-A-1,058,040.
  • CA-A-1,1 58,522 describes phosphate-free liquid dishwashing compositions containing a partially neutralized aminocarboxylic acid, a water-soluble salt of a nitrogen-free linear polymer containing carboxyl groups and a low-foaming nonionic surfactant.
  • CA-A-1,158,522 utilizes environmentally unacceptable nitrogen-containing aminocarboxylic salts, such as nitrilotriacetic acid or ethylene diamine tetraacetic acid.
  • GB-A-2,210,055 describes the use of polymer (polyacrylate) with zeolite to achieve performance. This composition also contains a chlorine source. Since the normal stabilizers are not chlorine stable, the composition of the GB-A-2,210,055 tends to stratify on standing. CA-A-1,058,040 also teaches the use of water-insoluble zeolites for the builder. When used as dishwashing detergents, because the zeolite is insoluble, deposits form on the glasses in the course of the cleaning operation.
  • chlorine-sensitive materials may now be added to the detergent compositions.
  • the object of the present invention is to provide a chlorine-free dishwashing detergent. It is a further object of the invention to provide such a dishwasher detergent which is also phosphate-free.
  • the objects of this invention may be accomplished by including, in a detergent composition, a copolymer containing, as polymerized units, maleic and, maleic anhydride, or salt thereof, and a hydrophobe, wherein the hydrophobe is a compound containing at least 4 carbon atoms, and preferably from 4 to 20 carbon atoms.
  • a chlorine-free, machine dishwashing detergent composition characterized in that it comprises from about 0.5 to 10 percent by weight of copolymer, or water-soluble salt thereof, containing, as polymerized units, from 20 to 75% by weight of the copolymer of maleic acid, maleic anhydride, or salt thereof, and from 25 to 80 % by weight of the copolymer of hydrophobe, wherein the hydrophobe is at least one compound selected from alkanes, alkenes, dienes, alkynes or aromatic compounds, and wherein said hydrophobe has at least 4 carbon atoms.
  • Chlorine-free as used herein in connection with the detergent composition of the present invention, means that the composition is free, or substantially free, of chlorine-releasing agents.
  • Hydrophobe refers to a monomer, oligomer, or polymer, the hydrophobe being copolymerized with monomers, oligomers, or polymers of maleic acid, maleic anhydride, or salts thereof, and being more hydrophobic than maleic acid, maleic anhydride, or the salts thereof.
  • the hydrophobe contains at least 4 carbon atoms and preferably from 4 to 20 carbon atoms.
  • the hydrophobe can be at least one monomer selected from alkanes, alkenes dienes, alkines or aromatic compounds. Examples of suitable hydrophobes include isobutylene, diisobutylene, styrene, decene and eicosene. The most preferred hydrophobe is diisobutylene.
  • the water-soluble salts of the copolymers for example the alkali metal salts or the ammonium or substituted ammonium salts thereof, can also be used.
  • the copolymers can be prepared by conventional methods of polymerization well known to those skilled in the art.
  • the amount of maleic acid, maleic anhydride, or salt thereof, contained in the copolymer is from about 20 to 75 percent, preferably from about 25 to 70 percent, based on the weight of the copolymer.
  • the amount of hydrophobe contained in the copolymer is about 25 to 80 percent, preferably from about 30 to 75 percent, based on the weight of the copolymer. Since the copolymer must be water-soluble, the amount of hydrophobe contained in the copolymer is dependent upon the hydrophobe selected and the water solubility of the resultant copolymer.
  • the concentration of copolymer in a detergent composition is from about 0.5 to 10 percent by weight of the detergent composition, and preferably from about 2 to 7 percent by weight.
  • the concentration of the copolymer in the detergent composition is dependent on the amount of other additives in the detergent composition which have an impact on the desired performance characteristics. For example, if a phosphate-containing compound is present in the detergent composition, the effective amount of copolymer necessary to achieve the desired performance may be lower than if no phosphate containing compound is present.
  • the detergent composition of this invention can be in the form of either a powder or liquid.
  • liquid also refers to a gel or a slurry.
  • the detergent composition of this invention may include conventional machine dishwashing detergent additives well known to those skilled in the art, except for chlorine releasing agents, in conventional use amounts.
  • the detergent composition of this invention may contain an alkali metal silicate at a concentration of from 0 to about 50 percent, preferably from about 1 to 10 percent, by weight of the detergent composition.
  • the alkali metal silicates which may be used in the composition of the present invention, can be metasilicates, designated as 1:1 M2o:SiO2 silicates to low M2O:SiO2 silicates such as 3.2:1 silicates, where M2O represents the alkali metal oxide portion of the silicate.
  • the more preferred alkali metal silicates are the sodium silicates.
  • alkali metal silicates are an optional component of the present invention
  • highly alkaline dishwashing detergents containing no silicates may attack aluminum pots and pans and other metal utensils. Therefore, silicates are beneficial when corrosion inhibition of metal parts is desired.
  • the detergent composition of this invention may optionally include a builder.
  • the level of builder can be from 0 to about 90 percent, and preferably from 20 to 90 percent, by weight of the detergent composition.
  • the builder concentration is dependent on whether the detergent is a liquid or a powder. Generally, a liquid composition will require less builder than a powder composition.
  • builders which may be employed in combination with the copolymers of the present invention include water-soluble inorganic builder salts such as alkali metal polphosphates, i.e., the tripolyphosphates and pyrophosphates, alkali metal carbonates, borates, bicarbonates, and hydroxides and water-soluble organic builders such as citrates, polycarboxylates and carboxylates.
  • zeolite may be added as a builder in amounts from 0 to about 40 percent, and preferably from about 20 to 40 percent by weight.
  • Inert diluents such as alkali metal chlorides, sulfates, nitrates, nitrites and the like, may also be used in the detergent composition.
  • examples of such diluents are sodium or potassium chloride, sodium or potassium sulfate, sodium or potassium nitrite, and the like.
  • water can be used as a diluent.
  • the amount of diluent used is generally an amount to bring the total amount of the additives in the detergent composition up to 100% by weight.
  • the detergent composition of this invention will generally contain a water-soluble detergent surfactant. Any water soluble anionic, nonionic, zwitterionic, amphoteric surfactant or combination thereof can be employed.
  • the quantity of surfactant used in the detergent formulation will depend on the surfactant chosen and will generally be from about 0 to about 10 percent, and preferably from about 1 to about 5 percent, by weight of the detergent composition.
  • Suitable anionic surfactants include soaps such as the salts of fatty acids containing about 9 to 20 carbon atoms, e.g. salts of fatty acids derived from coconut oil and tallow; alkyl benzene sulfonates - particularly linear alkyl benzene sulfonates in which the alkyl group contains from 10 to 16 carbon atoms; alcohol sulfates; ethoxylated alcohol sulfates; hydroxy alkyl sulfonates; alkenyl and alkyl sulfates and sulfonates; monoglyceride sulfates; acid condensates of fatty acid chlorides with hydroxy alkyl sulfonates and the like.
  • soaps such as the salts of fatty acids containing about 9 to 20 carbon atoms, e.g. salts of fatty acids derived from coconut oil and tallow; alkyl benzene sulfonates - particularly linear alkyl
  • nonionic surfactants include alkylene oxide (e.g. ethylene oxide) condensates of mono and polyhydroxy alcohols, alkyl phenols, fatty acid amides, and fatty amines; amine oxides; sugar derivatives such as sucrose monopalmitate; long chain tertiary phosphine oxides; dialkyl sulfoxides; fatty acid amides, (e.g., mono or diethanol amides of fatty acids containing 10 to 18 carbon atoms), and the like.
  • alkylene oxide e.g. ethylene oxide
  • fatty acid amides e.g., mono or diethanol amides of fatty acids containing 10 to 18 carbon atoms
  • Suitable zwitterionic surfactants include derivatives of aliphatic quaternary ammonium compounds such as 3-(N,N-dimethyl-N-hexadecyl ammonio) propane-1-sulfonate and 3-(N,N-dimethyl-N-hexadecyl ammonio)-2-hydroxy propane-1-sulfonate.
  • amphoteric surfactants examples include betaines, sulfobetaines and fatty acid imidazole carboxylates and sulfonates.
  • chlorine sensitive surfactants such as defoaming alkoxylated surfactants, may be used in the detergent compositions of the present invention. These surfactants not only offer the defoaming feature, but also enhance the sheeting action of the water from the ware.
  • the detergent may also contain up to about 5 percent by weight of conventional adjuvants such as perfumes, colorants and bacterial agents.
  • conventional adjuvants such as perfumes, colorants and bacterial agents.
  • stabilizers or viscosity modifiers such as clays and polymeric thickeners
  • the addition of polymeric or organic stabilizers and thickeners in a liquid composition was difficult because of the interaction between the stabilizers and thickeners and the chlorine. Generally, no stabilizer or thickener was used to disperse the solid phase, leading to stratification or settling of the solids to produce a hard pack at the bottom of the container. Because of the effective performance of the detergent compositions of this invention in the absence of chlorine, stabilizers or viscosity modifiers may be used effectively.
  • the detergent composition of this invention can be used in machine dishwashers as an aqueous solution at a concentration of about 0.2 to 1.5 percent, preferably from about 0.4 to 1 percent, by weight of the detergent.
  • the water temperature during the washing process should be about 26.7°C (80°F) to 60°C (140°F), and preferably from about 37.8°C (100°F) to 51.7°C (125°F).
  • the dishwashing tests were performed using a modified version of A.S.T.M. method D 3556-85, Standard Test Method for Deposition on Glassware During Mechanical Dishwashing .
  • This test method covers a procedure for measuring performance of household automatic dishwashing detergents in terms of the buildup of spots and film on glassware. Glass tumblers were given multiple cycles in a dishwasher, in the presence of food soils, and the levels of spotting and filming allowed by the detergents under test were compared visually.
  • a Kenmore dishwashing machine was used to perform the washing tests.
  • the bottom rack of the dishwasher was randomly loaded with 10-12 dinner plates and the top rack was randomly loaded with several beakers and cups.
  • Four new 283.5g (10 ounce) tumblers were placed randomly on the top racks as the test glasses.
  • Soil used in the test was a mixture of 80% Parkay Margarine and 20% Carnation Non-fat Dry milk. The amount of soil used for each test varied, but was usually 40 to 60 grams for the first wash.
  • the dishwashing machines had a short and a long cycle.
  • the long cycle, or normal wash consisted of a wash , a rinse, a second wash, two more rinses, and then a drying cycle.
  • the short cycle, or light wash consisted of a wash, two rinses and the drying cycle.
  • the machine was occasionally opened and a second detergent aliquot added. This was not always the case. Soil was not added when a second detergent dose was added. The machine was then allowed to run the full cycle including the drying time.
  • the test glasses were evaluated by placing them in light box equipped with a fluorescence light. The glasses were ranked according to the following scale:
  • the water hardness conditions for the supply water to the dishwasher could be varied, as could the detergent formulation and dosage.
  • the temperature of the supply water was maintained at 48.9°C (120° F).
  • Tables 3 to 13 show the performance results of detergent composition A
  • Tables 6 to 8 show the performance results of detergent composition B
  • Tables 9 to 11 show the performance results of detergent composition C
  • Tables 12 and 13 show the performance results of detergent composition D.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP19910305574 1990-06-20 1991-06-19 Machine dishwashing detergent composition Withdrawn EP0462829A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US541239 1983-10-12
US54123990A 1990-06-20 1990-06-20

Publications (2)

Publication Number Publication Date
EP0462829A2 true EP0462829A2 (fr) 1991-12-27
EP0462829A3 EP0462829A3 (en) 1993-07-07

Family

ID=24158755

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19910305574 Withdrawn EP0462829A3 (en) 1990-06-20 1991-06-19 Machine dishwashing detergent composition

Country Status (7)

Country Link
EP (1) EP0462829A3 (fr)
JP (1) JP3383669B2 (fr)
KR (1) KR920000913A (fr)
AU (1) AU657266B2 (fr)
CA (1) CA2044093A1 (fr)
NZ (1) NZ238581A (fr)
PL (1) PL290740A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995004804A1 (fr) * 1993-08-06 1995-02-16 La Marina Patent Holding S.A. Detergent sans phosphate ni chlore
EP0768370A3 (fr) * 1995-10-13 1999-07-07 Rohm And Haas Company Compositions de nettoyage contenant un dispersant de savon de chaux et son procédé de fabrication
WO2002064720A1 (fr) * 2001-02-01 2002-08-22 Basf Aktiengesellschaft Formulations de nettoyants pour empecher la decoloration d'articles en matiere plastique
WO2002064719A1 (fr) * 2001-02-01 2002-08-22 Basf Aktiengesellschaft Copolymeres pour empecher la corrosion du verre
WO2015000744A1 (fr) * 2013-07-04 2015-01-08 Basf Se Procédé de nettoyage de vaisselle

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5784730A (en) * 1980-11-13 1982-05-27 Nippon Oil & Fats Co Ltd Aqueous dispersion of metal soap
DE3744592C2 (de) * 1987-12-31 1996-04-18 Basf Ag Wasserlösliche Polymerisate enthaltende Geschirrspülmittel

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995004804A1 (fr) * 1993-08-06 1995-02-16 La Marina Patent Holding S.A. Detergent sans phosphate ni chlore
EP0768370A3 (fr) * 1995-10-13 1999-07-07 Rohm And Haas Company Compositions de nettoyage contenant un dispersant de savon de chaux et son procédé de fabrication
WO2002064720A1 (fr) * 2001-02-01 2002-08-22 Basf Aktiengesellschaft Formulations de nettoyants pour empecher la decoloration d'articles en matiere plastique
WO2002064719A1 (fr) * 2001-02-01 2002-08-22 Basf Aktiengesellschaft Copolymeres pour empecher la corrosion du verre
WO2015000744A1 (fr) * 2013-07-04 2015-01-08 Basf Se Procédé de nettoyage de vaisselle
US9938489B2 (en) 2013-07-04 2018-04-10 Basf Se Process for cleaning dishware

Also Published As

Publication number Publication date
JPH04226200A (ja) 1992-08-14
PL290740A1 (en) 1992-02-24
AU657266B2 (en) 1995-03-09
KR920000913A (ko) 1992-01-29
NZ238581A (en) 1993-09-27
AU7911791A (en) 1992-01-02
EP0462829A3 (en) 1993-07-07
JP3383669B2 (ja) 2003-03-04
CA2044093A1 (fr) 1991-12-21

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