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
  • C11D3/395—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
  • C11D3/16—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
  • C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions

Definitions

• the present invention is concerned with alkaline, aqueous cleaning concentrates and cleaning solutions comprising such concentrate. These cleaning concentrates/solutions are useful for the cleaning of food soils, and more specifically, are useful for the removal of milk soils from cold and hot surfaces without the use of phosphate builders.
• Dairy soils are composed of two components, the soil left behind from the milk processing operation and the soil left behind at the end of the cleaning operation.
• the soil resulting from the milk processing operation can vary widely in composition depending on, for example, the breed of cows, the time of year and the cow's food source. Additionally, if the surface contacting the milk is a heated surface, as used in pasteurization, it may be soiled with certain components in the milk which can be denatured, degraded, caramelized, or concentrated, thereby making soil removal even more difficult.
• the second soil results from the interaction between the milk soil residues and the chemicals in the cleaning solution.
• the problem can be compounded by poor rinsing and poor cleaning of the equipment, resulting in a substantial buildup of residual soil on the surfaces. This can lead to bacterial growth capable of causing a serious health risk when additional milk is processed through the equipment.
• hardness ions naturally present in the water source used for rinsing or for preparing the concentrate or cleaning solution can further compound the cleaning problem because of their tendency to react with the cleaning solution and inactivate the builder components of the cleaning solution.
• Sodium polyphosphates have been used as the builder of choice in previous aqueous cleaning solutions, but because of the increased use of liquid detergents, where sodium tripolyphosphate has a limited solubility, and increased environmental concerns on the use of phosphorous containing builders, alternative compositions have been investigated. However, with the decrease in phosphate use, performance of the cleaners has also decreased.
• US-A-4,579,676 claims a composition which purportedly avoids a decrease in the cleaning performance of phosphate free cleaning compositions through the use of a polyacrylic acid in combination with a soil-dispersing amount of a phosphinopolycarboxylic acid.
• the wash solutions are disclosed to be useful in the cleaning of cleaned-in-place food-processing equipment fouled with greasy or oily soils.
• the composition disclosed in US-A-4,579,676 continues to use the ecologically undesirable phosphorus in the form of phosphinopolycarboxylic acid.
• Belgium Patent 762,816 also discloses the use of a reduced amount of phosphorus in a cleaning solution.
• the solution described contains from 0 to 0.4 wt. % of a low level of alkali metal hydroxide, a sequestering agent containing amino and carboxyl groups, from 0.02 to 1 wt. % of condensed phosphate, from 0 to 0.3 wt. % alkali metal silicate and from 0.001 to 0.05 wt. % nonionic surfactant.
• This composition is supposedly useful for cleaning, with high efficiency and less susceptibility to contamination, heat exchangers used for pasteurizing milk and other dairy and food industry equipment.
• a third patent, EP-B-0,268,873, discloses a cleaning composition based on a quaternary ammonium compound, an alkyl ether carboxylic acid, an alkali metal hydroxide, and a complex-forming amino-polycarboxylic acid.
• This cleaning composition is purportedly useful for the food industry, especially dairies, does not foam, and also has some disinfectant properties.
• the present invention is directed to an aqueous cleaning concentrate, formulated as a water-dilutable aqueous concentrate, comprising (i) an alkali metal hydroxide, (ii) an active chlorine source, (iii) a water-soluble copolymer comprising units of a monoethylenically unsaturated dicarboxylic acid and at least one comonomer selected from monoethylenically unsaturated monocarboxylic acids and carboxyl-free monoethylenically unsaturated monomers and, optionally, (iv) an alkali metal silicate.
• the present invention is also directed to aqueous cleaning solutions that do not contain any phosphorus, are suitable for the removal of food soils, and perform effectively at high water hardness levels.
• a cleaning concentrate which comprises:
• the present invention enables the provision of cleaning concentrates/solutions that do not contain any phosphorus, are suitable for the removal of food soils, and perform effectively at high water hardness levels, this being achieved by the use of the stated copolymers in an alkaline, chlorine-containing composition, with said copolymer aiding in the complete removal of residual fatty and oily soil.
• the copolymers used in this invention have a greater affinity for calcium as compared to previously described acrylic homopolymers. Furthermore, since there is not enough polymer in the detergent bath to sequester all the hardness ions, especially at high hardnesses, the polymer must be interacting with the calcium at a specific location, such as the substrate surface, and not improving the cleaning by dispersing more soil or by interacting with the calcium in the aqueous media.
• the theory of this invention is presented here as a possible explanation of the surprising results obtained, and in no way is intended to limit the scope of this invention.
• copolymers used in this invention, to available chlorine, these copolymers could be applicable to any situation where a soil removal aid in an alkaline, chlorinated liquid is needed.
• the copolymer used in this invention contains, as copolymerized monomer units, from 5 to 70% by weight of the monoethylenically unsaturated dicarboxylic acid or salt or anhydride thereof, and from 95 to 30% by weight of the comonomer(s), e.g. the monoethylenically unsaturated monocarboxylic acid.
• the preferable range is from 10 to 30% by weight of the monoethylenically unsaturated dicarboxylic acid or salt or anhydride thereof and from 90 to 70% by weight of the comonomer(s), e.g.
• the monoethylenically unsaturated monocarboxylic acid and the more preferable range is from 15 to 25% by weight of the monoethylenically unsaturated dicarboxylic acid or salt or anhydride thereof and from 85 to 75% by weight of the comonomer(s), e.g. the monoethylenically unsaturated monocarboxylic acid.
• Suitable monoethylenically unsaturated dicarboxylic acids include those containing from 4 to 6 carbon atoms per molecule, their salts, e.g. their alkali metal and ammonium salts, and the anhydrides of the cis dicarboxylic acids.
• suitable monomers include maleic acid, itaconic acid, mesaconic acid, fumaric acid, citraconic acid and the anhydrides of cis dicarboxylic acids, such as maleic anhydride.
• Maleic anhydride is the more preferred of these monomers.
• Suitable monoethylenically unsaturated monocarboxylic acids contain from 3 to 6 carbon atoms per molecule and include acrylic acid, methacrylic acid, vinyl acetic acid, crotonic acid and acryloxypropionic acid.
• the more preferred monoethylenically unsaturated monocarboxylic acid is acrylic acid.
• Suitable carboxyl-free monoethylenically unsaturated monomers include alkyl esters of acrylic or methacrylic acids such as methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate and isobutyl methacrylate; hydroxyalkyl esters of acrylic or methacrylic acids such as hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, and hydroxypropyl methacrylate; acrylamide; methacrylamide; N-tertiary butyl acrylamide; N-methyl acrylamide; N,N-dimethyl acrylamide; acrylonitrile; methacrylonitrile; allyl alcohol; allyl sulfonic acid; allyl phosphonic acid; vinylphosphonic acid; dimethylaminoethyl acrylate; dimethylaminoethyl me
• the concentration of carboxyl-free monoethylenically unsaturated monomers can be from 0 to about 80% by weight of the total monomer concentration.
• the concentration is typically up to 35% by weight and is dependent upon the solubility of the particular monomer in the reaction mixture.
• copolymers may be made by a heel charge process whereby the monoethylenically unsaturated dicarboxylic acid is placed in a reactor, to which a feed of initiator and comonomer(s), e.g. monoethylenically unsaturated monocarboxylic acid, is added, or a co-feed process, whereby the monoethylenically unsaturated dicarboxylic acid is fed into the reactor concurrently with the comonomer(s), e.g. the monoethylenically unsaturated monocarboxylic acid.
• This co-feed process is disclosed in European Patent Application No. 90305346.0.
• the range of molecular weights, Mw, for the copolymer, as measured by aqueous gel permeation chromatography (GPC), is from about 4,000 to 100,000, preferably from about 10,000 to 30,000, and more preferably from about 10,000 to 25,000.
• the alkali metal hydroxide can be any type commonly used in the art such as sodium hydroxide, potassium hydroxide or mixtures thereof.
• the chlorine source can be either organic or inorganic including alkali metal and alkaline earth metal hypochlorites, hypochlorite addition products, chloramines and chlorimines, chloramides and chlorimides.
• these compounds include sodium hypochlorite, potassium hypochlorite, monobasic calcium hypochlorite, dibasic magnesium hypochlorite, chlorinated trisodium phosphate dodecahydrate, potassium dichloroisocyanurate, trichlorocyanuric acid, sodium dichloroisocyanurate dihydrate, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfamide, Chloramine T, Dichloramine T, Chloramine B, Dichloramine B, chlorine gas or mixtures thereof.
• the more preferred source of chlorine is sodium hypochlorite.
• the cleaning concentrate of the present invention contains: from 2.5 to 35% alkali metal hydroxide, preferably from 5 to 15%, and more preferably 10%; from 1 to 5% available chlorine, preferably from 2 to 4%, and more preferably 3%; from 0.25 to 20% polymer solids, preferably from 3 to 15%, and more preferably 5.1%; and the remainder is water or other components commonly known to those skilled in the art.
• alkali metal silicate e.g. sodium silicate
• alkali metal silicate e.g. sodium silicate
• the cleaning concentrate and/or cleaning solution of the present invention are any of the usual adjuvants found in detergents of this type such as inorganic phosphates, citrates, ethylenediaminetetraacetic acid, nitrilotriacetic acid, carboxyalkylamines, surfactants, and homopolymers of polyacrylic acid.
• the cleaning concentrate may be diluted to about 0.1 to 10% with water.
• Example provides a representative procedure for the synthesis of the polymers used in the formulations of the present invention and all percentages recited are percentages by weight unless specified otherwise.
• the resultant pH 6.7 polymer solution had a solids content of 46.0%. Based on gel permeation chromatography (GPC), the weight average molecular weight (Mw) was 15,200 and the number average molecular weight (Mn) was 7440. Residual maleic acid content was 0.2% by weight and residual acrylic acid content was 0.01% by weight, the percentages being based on the total theoretical weight of solids.
• GPC gel permeation chromatography
• a detergent formulation utilized for the testing of this invention had the following composition: 10% sodium hydroxide, 3% available chlorine, and 5.1% polymer solids. Sodium hydroxide levels of 14% were also employed in some tests to assess the effect of higher levels of alkali on the cleaning performance as compared to the use of the polymer to boost cleaning. Sodium silicate was also used in some of the testing at a level of 4.7% sodium silicate solids, which is equivalent to approximately 3.3% silicate solids (SiO2). The performances of these detergent compositions were compared to a typical commercial product, Interest (trademark of the Diversey-Wyandotte Corporation) detergent, which is a phosphate-based composition.
• the detergents both those of this invention and the Interest detergent, were tested at concentrations of from about 0.1% use level (on an as is basis) to about 2% detergent concentration in the bath.
• the detergents were tested predominately against a multicycle-deposited cold milk soil.
• the substrates soiled in the testing were 304 stainless steel panels measuring 2.54 cm x 7.62 cm x 0.094 cm (1" x 3" x 0.037").
• the water used for dilution of the detergent and cleaning of the panels contained from 100 ppm to 600 ppm hardness as CaCO3 and 225 ppm sodium bicarbonate, regardless of the water hardness.
• the cold milk soiled panels were prepared by precleaning them with methanol, immersing them in a 1% solution of Interest detergent for 15 minutes, rinsing them with deionized water and then drying them.
• the chemically cleaned panels (6 at a time) were then immersed in fresh whole milk (Vitamin A&D - not skim or low fat) to about 7/8ths of their total length and agitated for exactly 15 minutes. This was the soiling portion of the test.
• the panels were removed, rinsed in 48.9 °C (120°F) running tap water with a hardness of 200 ppm as CaCO3.
• Each test panel was then cleaned in detergent solution maintained at 60°C in a shaker bath.
• the detergent solution contained the water hardness and detergent concentrations listed in the Tests.
• the detergent solution also contained two drops of milk added as an additional stress to the test.
• the test panels were removed and rinsed in 48.9°C (120°F) running tap water. This constituted one cycle.
• the panels were rinsed in tap water for the final time, they were immersed in a 1% protein dye solution for 2 to 3 minutes (the protein dye used was Safranine O).
• the dye solution immediately attached to any milk soil present that had not been removed by the detergent solutions.
• varying degrees of red stain resulted, the darker the red stain the more milk soil left on the panels.
• the stained panels were then dried with forced hot air and graded using the following scale: are useful for the removal of milk soils.
• the results also show that the copolymers in accordance with this invention are superior to previously described acrylic homopolymers, even at equivalent molecular weights, when higher (>300 ppm) water hardnesses are used.

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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)

Applications Claiming Priority (2)

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Citations (4)

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• 1990
  • 1990-07-30 IE IE275990A patent/IE902759A1/en unknown
  • 1990-07-31 NZ NZ234721A patent/NZ234721A/en unknown
  • 1990-07-31 DD DD90343178A patent/DD298422A5/de not_active IP Right Cessation
  • 1990-07-31 AU AU60047/90A patent/AU639007B2/en not_active Ceased
  • 1990-07-31 EP EP90308404A patent/EP0442191A1/fr not_active Withdrawn
  • 1990-08-02 CA CA002022555A patent/CA2022555C/fr not_active Expired - Fee Related
  • 1990-08-02 ZA ZA906079A patent/ZA906079B/xx unknown
  • 1990-08-13 PT PT94977A patent/PT94977A/pt not_active Application Discontinuation
  • 1990-10-04 JP JP2267525A patent/JP2877933B2/ja not_active Expired - Lifetime

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