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WO1999061545A1 - Diesel engine antifreeze composition - Google Patents

Diesel engine antifreeze composition Download PDF

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Publication number
WO1999061545A1
WO1999061545A1 PCT/US1999/011324 US9911324W WO9961545A1 WO 1999061545 A1 WO1999061545 A1 WO 1999061545A1 US 9911324 W US9911324 W US 9911324W WO 9961545 A1 WO9961545 A1 WO 9961545A1
Authority
WO
WIPO (PCT)
Prior art keywords
antifreeze
sodium
weight
salt
coolant
Prior art date
Application number
PCT/US1999/011324
Other languages
French (fr)
Inventor
David E. Turcotte
Frances E. Lockwood
Original Assignee
Ashland Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ashland Inc. filed Critical Ashland Inc.
Priority to AU40943/99A priority Critical patent/AU743301B2/en
Priority to CA002333046A priority patent/CA2333046C/en
Publication of WO1999061545A1 publication Critical patent/WO1999061545A1/en
Priority to AU35029/00A priority patent/AU772428B2/en
Priority to BRPI0010276-8B1A priority patent/BR0010276B1/en
Priority to CA002363660A priority patent/CA2363660C/en
Priority to CNB008059918A priority patent/CN1200990C/en
Priority to EP00913616A priority patent/EP1159372B1/en
Priority to MXPA01008616A priority patent/MXPA01008616A/en
Priority to DE60045442T priority patent/DE60045442D1/en
Priority to PCT/US2000/004850 priority patent/WO2000050532A1/en
Priority to DK00913616.9T priority patent/DK1159372T3/en
Priority to AT00913616T priority patent/ATE493481T1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C—CHEMISTRY; METALLURGY
    • C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
    • C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
    • C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/20—Antifreeze additives therefor, e.g. for radiator liquids

Definitions

  • This invention relates to extending diesel engine coolant lifetime through polymeric polycarboxylate secondary silicate stabilization. More particulary, this invention relates to an antifreeze formulation for inhibition and prevention erosion and corrosion of aluminum and the corrosion of other metals exposed to an aqueous liquid in automotive coolant systems. The formulation further inhibits mineral scale.
  • the novel antifreeze formulation comprises a mixture of polymeric polycarboxylates, azoles, nitrate and nitrite salts, phosphates, siloxane stabilized silicates and transition metal compounds which provide a synergistic protective effect against the cavitation corrosion of aluminum in aqueous liquids reducing the corrosion rate and is effective at relatively low concentrations and varying pH ranges .
  • selected polymeric polycarboxylates not only significantly reduces glycol based coolant cavitation erosion-corrosion, heat rejecting aluminum corrosion, and hard water precipitates and scale, it has been discovered that selected polymeric polycarboxylates in combination with siloxane stabilized silicates enhance secondary silicate stabilization leading to improvement in aluminum corrosion protection and coolant life when utilized with selected amounts of the above- identified additives.
  • the formulations are particularly suitable for automotive applications .
  • silicate as a corrosion inhibitor.
  • Silicates are particularly useful in protecting aluminum automotive cooling system components.
  • the silicate corrosion inhibitors generally also use a phosphate, usually in the form of an alkali metal salt, to help protect metal cooling system parts and also as a buffer to control the pH of the coolant.
  • phosphate salts are used to help maintain a stable alkaline environment from which multiple corrosion inhibitors can most effectively function.
  • antifreeze/coolant is sold at nearly one-hundred percent glycol content. This concentrated packaging allows for flexibility so that the user can dilute the antifreeze/coolant, as needed, with available water to obtain the required freeze/boil protection.
  • corrosion protection is needed over the entire dilution range.
  • Engine coolants primarily ethylene glycol or propylene glycol based solutions, must transfer heat from operating aluminum engines while inhibiting corrosion. Older automotive engines did not have aluminum components and thus, the traditional antifreeze/coolant compositions may produce corrosion in heat rejecting aluminum or aluminum alloy components.
  • the cavitation erosion-corrosion of aluminum water pumps upon exposure to aqueous systems such as water-cooled internal combustion engine coolants is a relatively new development.
  • U.S. Patent 4,717,495 by Hercamp et al . teaches a sodium-free buffer solution.
  • U.S. Patent No. 4,548,787 discloses the use of a combination water soluble phosphate with tungstae, selenate and molybdate for protection against cavitation erosion-corrosion on aluminum.
  • U.S. Patent No. 4,404113 discloses the use of polyhydric alcohols as corrosion inhibiting and cavitation reducing additives for coolants.
  • U.S. Patent No 4,487,712 discloses the use of polyacrylic acid as a silicate stabilizer to inhibit gelation which is a silicate depletion mechanism which can occur separately from hard water precipitates.
  • polymeric polycarboxylates has been shown to significantly reduce glycol based coolant cavitation erosion- corrosion as set forth in U.S. Patent Nos. 5,288,419 and 5,290,469; to reduce heat rejecting aluminum corrosion as set forth in U.S. Patent Nos. 5,320,670 and 5,290,467; and to reduce hard water precipitates and scale as set forth in U.S. Patent Nos. 5,330,670 and 5,290,468; all of which are hereby incorporated by reference.
  • U.S. Patent No. 4,440,721 discloses the combination of a water-soluble phosphate with a water soluble molybdate, tungstate, or selenate for providing a protective effect against the cavitation corrosion of aluminum in aqueous liquids. While alkali metal molybdates and the soluble salts of tungstic and selenic acids have been used in antifreeze compositions to prevent the corrosion of metals, particularly cast iron, soluble salts of molybdic, tungstic and selenic acids act to retard the corrosion of aluminum, particularly the cavitation erosion-corrosion of aluminum water pumps .
  • such a formulation would be designed for modern aluminum engine based passenger car cooling systems.
  • the formulation must be liquid, easily miscible with diluted antifreeze in the cooling system, protect all cooling system metals, have a useful shelf life, not harm automotive finishes or paint and not promote excessive cooling system foam.
  • the present invention has met the above-described need by providing an antifreeze/coolant composition using selected polymeric polycarboxylate additives which reduce corrosion over the entire dilution range without creating precipitates.
  • This composition is soluble in water, alcohol, and alcohol/water mixtures, is compatible with other commonly used antifreeze/coolant components, does not corrode or damage automotive cooling systems and is effective at relatively low concentrations.
  • the present corrosion inhibition formulations are effective in reducing corrosion in the entire range of cooling system metals, including heat rejecting aluminum, aluminum alloys, copper, steel, cast iron, brass, solder and the like.
  • water-soluble salts of an acid elected from the group consisting or molybdic, tungstic and selenic acids or salts thereof, in combination with a water-soluble phosphate and a polymeric polycarboxylate provide a synergistic improvement in the retardation or the cavitation erosion- corrosion of aluminum water pumps and other metal engine components when used in contact with aqueous liquids, particularly aqueous antifreeze compositions containing a water-soluble alcohol freezing point depressant.
  • the present invention provides long life corrosion inhibition antifreeze/coolant compositions by using certain polymeric polycarboxylate additives in a synergistic combination with stabilized silicate
  • siloxane and other selected compounds, primarily the combination of nitrates and nitrates and an increased amount of molybdate which reduces coolant cavitation erosion-corrosion, heat rejecting aluminum corrosion, and hard water precipitates and scale.
  • polymeric polycarboxylates enhance secondary silicate stabilization leading to improvement in aluminum corrosion protection and prolonged coolant life as compared to conventional silicon based coolants.
  • the present corrosion inhibition formulations are effective in reducing corrosion in the entire range of cooling system metals, including heat rejecting aluminum, aluminum alloys, copper, steel, cast iron, brass, solder and the like. This formulation is soluble in alcohol, alcohol/water mixtures and in water alone and exhibits excellent stability characteristics.
  • the most preferred antifreeze/coolant composition is a silicate-phosphate type having a pH of about 10.5 and having about 94% antifreeze grade glycols and about 3% corrosion inhibitors, with the balance being water.
  • the freezing point depressant utilized in the antifreeze compositions of the invention can be any suitable water-soluble liquid alcohol used heretofore in formulating antifreeze compositions.
  • the water-soluble alcohol contains 1 to about 4 carbon atoms and 1 to about 3 hydroxy groups .
  • Ethylene glycol is preferred as the freezing point depressant and especially the commercially available mixtures containing largely ethylene glycol and a small amount of diethylene glycol .
  • the commercial mixture generally contains at least 85 to 95 percent by weight of ethylene glycol with the remainder being diethylene glycol and small amounts of substances which are incidentally present such as water.
  • Other water- soluble liquid alcohol can be admixed with ethylene glycol but such mixtures usually are not preferred.
  • Inexpensive commercially available water soluble alcohols can also be used such as methyl, ethyl, propyl, and isopropyl alcohol alone or in mixtures .
  • the concentrated corrosion inhibitor formulations of the present invention is a water-based mixture of polymeric polycarboxylates, nitrate and nitrite salts, molybdates, phosphate, azoles, stabilized silicates and transition metal compounds .
  • other components including defoamers, dyes, buffering agents, biocides, detergents, and the like may be added to the present formulation.
  • a water soluble phosphate level is given on the basis of hydrogen phosphate, alkali metal salts are typically used. Alkaline earth or ammonium slats are also possible alone or in combination therewith.
  • Nitrates and nitrites are typically introduced as an alkali salt although acid, alkaline earth or ammonium salts could be utilized including potassium, sodium or salts alone or in combinations therewith.
  • the azoles include tolytriazole, benzotriazole, mercaptobenzothizole including mixtures and other substituted azoles.
  • Stabilized silicate typically referred to as siloxane compounds, are of the type described in U.S. Patent Nos. 4,354,002, 4,362,644, and/or 4,370,255, hereby incorporated by reference.
  • Suitable defoamers include PLURONIC ® L-61, PATCOTE ® 415 and other surfactants including silicone types. The synergistic combination of phosphate, molybdate and stabilized silicate is described in U.S. Patent Nos. 4,548,787, 4,707,286, and 4 , 440 , 721 , hereby incorporated by reference.
  • silicate-phosphate type coolants these additives are useful in silicate-borax, silicate phosphate and borax coolants, organic acid, and organic acid silicate hybrid type coolants, and the like.
  • the corrosion inhibitor formulations are compatible with other commonly used antifreeze/coolant components and are effective at relatively low concentrations.
  • Each of the preferred ingredients of the synergistic antifreeze formulation, whether mandatory or optional, is discussed below:
  • the preferred class of stabilizing polymeric polycarboxylates are based on polyacrylic acid (PAA) and/or polymaleic acid (PMA) . These polymeric polycarboxylates are compatible with other components in the typical antifreeze/coolant composition, and present no additional toxicity or disposal concerns .
  • the molecular weight distribution of useful materials may average about one hundred grams/mole to about three million grams/mole. Chemically, the materials should be based on polymers and copolymers of acrylic acid and/or maleic acid, including any modifiers, such as alcohols.
  • the polycarboxylates used in the present invention have a molecular weight range of from about 1,200 to about 250,000, with a preferred range of from 500 to 12,000. More specifically, the most preferred additives have average molecular weights in the range of about 500 to about 4,000, and more specifically about 1300 to about 1800 and about 300 to about 4600.
  • polycarboxylates within the context of the present invention it is understood to encompass those watersoluble homo- and copolymers having at least one monomeric unit containing C 3-6 monoethylenically unsaturated mono- or dicarboxylic acids or their salts.
  • Suitable monocarboxylic acids of this type are for example, acrylic acid, methacrylic acid, ethacrylic acid, vinylacetic acid, allylacetic acid, and crotonic acid.
  • the preferable monocarboxylic acids from this group are acrylic acid and methacrylic acid.
  • a further component of the polycarboxylate comprises monoethylenically unsaturated C 4-s dicarboxylic acids, for example, maleic acid, itaconic acid, citraconic acid, mesaconic acid, fumaric acid, or methylenemalonic acid.
  • the preferred acid is maleic acid.
  • a secondary alcohol such as isopropanol
  • X COOH, COONa ⁇ , ethylvinylether, isobutylene, vinyl acetate, acrylamide, or styrene
  • the preferred polycarboxylates are a copolymer of acrylic acid and maleic acid, or their sodium salts, said copolymer having a molecular weight of 3000, and a sodium salt of polyacrylic acid modified with a secondary alcohol such as isopropanol, said polymer having a molecular weight of 4000.
  • the polycarboxylates used in the present invention are obtained by methods well known to those skilled in the art.
  • the general method of synthesis is via free acid radical polymerization.
  • the polymerization may be carried out in an aqueous medium, in the presence of polymerization initiators, with or without regulants.
  • the polymerization can take various forms,- for example, the monomer (s) can be polymerized batchwise in the form of aqueous solutions. It is also possible to introduce into the polymerization reactor a portion of the monomer (s) and a portion of the initiator, to heat the mixture in an inert atmosphere to the polymerization temperature and then to add the remaining monomer (s) and initiator to the reactor at the rate of polymerization.
  • Polymerization temperatures range from 20°C to 200°C. At temperatures above 100°C, pressure vessels are employed.
  • the carboxyl containing monomers can be polymerized in the free carboxylic acid form, in the partial neutralized form, or completely neutralized.
  • the neutralization is preferably effected with alkali metal or ammonium base .
  • the polymerization initiators used are preferably water soluble free radical formers such as hydrogen peroxide, peroxodisulfates and mixtures of the two.
  • the polymerization may also be started with water insoluble initiators such as dibenzoyl peroxide, dilaurylperoxide, or azodiisobutyronitrile .
  • the polymerization may be carried out in the presence of regulants .
  • regulants include water soluble mercaptans, ammonium formate, and hydroxylammonium sulfate.
  • Polymeric polycarboxylate materials which are useful in the present invention include Belclene water treatment additives from CIBA-GEIGY ® , Colloid additives from COLLOIDS ® , Inc., GOOD-RITE ® polyacrylates and CARBOPOL ® resins from BF GOODRICH ® and the like.
  • Examples of the polycarboxylates which may be used in the present invention are those marketed by BASF ® under the trademark SOKALAN ® polycarboxylates, which are available in aqueous polymer solutions . More particularly, the SOKALAN ® polyacrylic dispersants are copolymer carboxylate dispersants.
  • SOKALAN ® polycarboxylates are acrylic/maleic copolymers and other copolymers of either maleic or acrylic acid. These polycarboxylates are generally fully neutralized.
  • the suffix "S" is a designation used to indicate free acids in the SOKALAN ® range.
  • SOKALAN ® CP10, CPlOs, or CP12s has been shown to be particularly effective at about 0.05 to about 0.20 weight percent in one inhibitor concentrate, other levels of additive and different polycarboxylates may also be used.
  • SOKALAN ® 10 has an average relative molecular weight of about 4,000, and comprises a secondary alcohol modified polyacrylic acids; whereas SOKALAN ® 12 has an average relative molecular weight of about 3,000 and comprises a sodium salt of a copolymer of acrylic acid and maleic acid.
  • the polymeric polycarboxylate is preferably present in the formulation in an amount of about 0.001 to about 10.0 percent by weight, and more preferably in an amount of about 0.01 to about 0.1 percent by weight.
  • the polymeric polycarboxylate is effective at enhancing stability at relatively low concentrations, generally about 100 to about 1000 ppm per total volume of inhibitor concentrate.
  • the most preferred polycarboxylates are the K-700 polyacrylate polymers from BF GOODRICH ® which include the GOOD-RITE ® K-732 AND GOOD-RITE ® K-752 polyacrylate polymers . Both are mixtures of sodium polyacrylate and polyacrylic acid in water as set forth and described in the copies of the Material Safety Data sheets as set forth in the Information Disclosure Document and incorporated by reference herewith. These polymers are similar, while differentiated by their molecular weight.
  • the GOOD-RITE ® K-752 polyacrylate is a water soluble acrylic acid polymer supplied as a clear to hazy, colorless to amber colored, and ranging from about 62% to about 64% total solids solution in water averaging about 63%, with the active solids being about 62.5% having a specific gravity of about 1.23.
  • the molecular weight (GPC M ⁇ ) is about 2100.
  • the pH ranges from about 2.2 to 3.0 and averages about 2.6.
  • Viscosity (CP at 25°C) ranges from between about 400 to about 1,400, and averages about 950.
  • the GOOD-RITE ® K-732 polyacrylate is a water soluble acrylic acid polymer supplied as a clear to hazy, colorless to amber colored, and ranging from about 49% to about 51% total solids solution in water and averaging about 50%, with the active solids being about 49.5% having a specific gravity of about 1.2.
  • the molecular weight (GPC M w ) is about 5,100.
  • the pH ranges from about 2.2 to 3.0 and averages about 2.6.
  • Viscosity (CP at 25°C) ranges from between about 250 to about 500, and averages about 350.
  • Combinations of the polycarboxylates may also be utilized in the present invention such as a mixture of a secondary alcohol modified polyacrylic acid, a sodium salt of a copolymer of acrylic acid and maleic acid and/or mixtures of sodium polyacrylate and polyacrylic acid in water. These combinations having a molecular weight of less than 10,000 are deemed to be suitable polycarboxylate additives .
  • metal salt corrosion inhibitors preferably alkali metal salts known in the prior art can be usefully added to the aqueous liquids or the invention.
  • metal salt corrosion inhibitors include the water-soluble: nitrates, nitrites, silicates, carbonates, sodium silicate, sodium nitrate, potassium carbonate, ammonium silicate.
  • a nitrate in combination with a nitrite is used in the preferred composition in a higher concentration for heavy duty applications in diesel engines than typically used in gasoline engines.
  • the source of the nitrate and nitrite ions can be any water- soluble nitrate or nitrite such as the alkali metal nitrates and nitrites .
  • Nitrate salts suitable in the present invention include, sodium nitrate, potassium nitrate, magnesium nitrate, calcium nitrate, lithium nitrate, mixtures thereof and the like.
  • Nitrite salts suitable in the present invention include, sodium nitrite, potassium nitrite, magnesium nitrite, calcium nitrite, lithium nitrite, mixtures thereof and the like. Any compatible salt may be used including sodium, potassium, lithium, magnesium, calcium and the like.
  • the most preferred nitrate salt is sodium nitrate and the preferred nitrite is sodium nitrite.
  • nitrate salts may be supplied.
  • the pH of the total composition may be adjusted by addition of nitric acid ions.
  • the reaction of nitrate acid and basic salts contained in the composition will result in liberation of free carboxylic acid and the formation of nitrate salts .
  • Nitrate salts serve to inhibit corrosion in the formulations of the present invention and aids in the protection of aluminum.
  • the nitrate salt is preferably present in the formulation in an amount of about 0.01 to about 10.0 percent by weight, more preferably in an amount of about 0.1 to about 3.0 percent by weight, and most preferably in an amount of about 0.1 to about 1.0 percent by weight .
  • Nitrite salts are especially good for preventing heavy duty cylinder linings from pitting. They are good oxidizers when used with ferrous metals for protecting surfaces such as cylinder liner sleeves and other ferrous components of diesel engines.
  • the nitrites have a higher oxidation state than the nitrates and are ions are depleted at a higher rate making them more expensive than the nitrate salts,- however, the nitrites are especially good in reducing pitting by forming a coating on the ferrous surface.
  • the nitrates form nitrites upon oxidation.
  • the nitrite salt is preferably present in the formulation in an amount of about 0.01 to about 10.0 percent by weight, more preferably in an amount of about 0.1 to about 3.0 percent by weight, and more preferably in an amount of about 0.1 to about 1.0 percent by weight.
  • the preferred embodiment of the present formulation utilizes a greater amount of water soluble nitrite than water soluble nitrates. More specifically, one preferred formula utilizes water soluble nitrates in a range of from about 0.05 to about 0.30 percent by weight, and water soluble nitrites in a range of from about 0.30 to about 0.60 percent by weight, representing about a 2:1 ratio.
  • Azoles are present in the formulation to inhibit corrosion of yellow metal like copper and brass. Brass thermostats and radiator caps are common as well as copper and brass radiators.
  • the azole compound providing protection for copper and brass from corrosion is selected from among the water- soluble triazoles, pyrazoles, imidazoles, isooxazoles, isothiazoles, thiazoles, thiadiazole salts, and the like. Generally, the alkali metal salts are used.
  • Specific preferred azole compounds include 1, 2, 3 -benzotriazole; 1, 2, 3 -tolyltriazole,- sodium 2 -mercaptobenzothiazole; and sodium 2-mercaptobenzimidazole .
  • Azole compounds suitable in the present invention include, salts of mercaptobenzothiazole, salts of tolytriazole, benzotriazole, mixtures thereof and the like. Typically, these azoles are preferably present in a fifty percent concentration. However, one preferred azole compound consists of the salts of mercaptobenzothiazole and salts of tolytriazole. More particularly, one preferred azole compound is a mixture of sodium mercaptobenzothiazole and sodium tolytriazole which may be used in about a 3 to 1 ratio.
  • the azoles are preferably present in the ormulation in an amount of about 0.01 to about 10.0 percent by weight, and more preferably in an amount of about 0.05 to about 1.0 percent by weight.
  • the azole compound is used in amounts of about 0.1 parts to about 0.5 parts by weight, preferably about 0.1 to about 0.4 parts by weight, based on 100 parts by weight of the aqueous liquid.
  • the water-soluble molybdate which is preferred for use in the aqueous systems of the present invention can be any salt of molybdic acid which is readily soluble in water.
  • These include both alkali metal and alkaline earth metal molybdates as well as ammonium molybdate, the term "alkali molybdate" being used in a broad sense so as to include alkali metal, alkaline earth metal and ammonium molybdates .
  • Examples of useful molybdates are sodium molybdate . potassium molybdate, lithium molybdate and ammonium molybdates including ammonium dimolybdate and ammonium heptamolybdate .
  • Alkali molybdate compounds, sodium molybdate and potassium molybdate are preferred because of their availability and compatibility with the aqueous system as well as for economic reasons .
  • concentration of the molybdate ion will vary depending upon the degree of hardness of the aqueous system, the temperature, and the amount of dissolved oxygen in the aqueous system. While concentrations of the molybdate ion above about 0.5 parts by weight per 100 parts by weight of aqueous liquid can be employed, in most instances concentrations of molybdate ion above this limit normally do not provide significant improvements in the inhibitive characteristics or the aqueous system and are undesirable for economic reasons.
  • Transition metal compounds suitable for use in the present invention include, disodium salt dehydrate of molybdic acid, sodium molybdate 2H 2 0, molybdenum trioxide, silicoheteropolymolybdates, phosphoroheteropolymolybdates, mixtures thereof and the like. Any compatible transition metal may be used, including for example, molybdate, cobalt, cerium, mixtures thereof and the like. In addition, any acid salt may be used including sodium, potassium, lithium, calcium, magnesium and the like. The most preferred transition metal compound is the disodium salt dehydrate of molybdic acid or sodium molybdate 2H 2 0.
  • Transition metal acids are used to inhibit corrosion in formulations of the present invention.
  • the transition metal compound is preferably present in the formulation in an amount of about 0.001 to about 10.0 percent by weight, and more preferably in an amount of about 0.1 to about 0.5 percent by weight.
  • the molybdate ion is employed in amounts so as to provide a concentration in the aqueous system of at least about 0.01 parts by weight per 100 parts by weight of aqueous liquid. Preferably about 0.15 to about 0.2 parts by weight per 100 parts by weight of molybdate based upon said aqueous liquid are employed. More molybdate is utilized in the present diesel engine formulation than typically used in automotive engine coolants.
  • Both inorganic and organic water-soluble phosphorus compounds are useful in inhibiting the cavitation erosion corrosion of aluminum in contact with aqueous liquids.
  • the water-soluble phosphates are used generally in amounts so as to provide a concentration of about 0.5 to about 2 parts by weight per 100 parts by weight of the aqueous liquid.
  • These compounds include the preferred water-soluble alkali metal salts of orthophosphoric acid, pyrophosphoric acid, and metaphosphoric acid.
  • Orthophosphoric acid being tri-basic forms three series of salts, potassium dihydrogen phosphate, disodium hydrogen phosphate, and trisodium phosphate.
  • Useful organic phosphates include the oxyesters of phosphoric acid, as well as the amides and triesters thereof.
  • the most common phosphorus acid esters which are useful are the mono-, di-, and tri-esters of orthophosphoric acid. These can be alkyl phosphates , aryl phosphates and mixed alkyl-aryl phosphates.
  • Representative alkyl groups having 1 to about 18 carbon atoms which can be present in the alkyl phosphates include methyl, ethyl, propyl, isopropyl and n-butyl, isobutyl, etc.
  • Representative substituted alkyl groups which can be present in the phosphorus esters include said alkyl groups substituted with halogen, especially chlorine and fluorine, and with alkoxy groups.
  • substituted alkyl groups include butoxyethyl, 2-chloroethyl, 2-nuoroethyl, etc.
  • groups which can be present in the phosphorus esters include alkyl groups substituted with halogen, especially chlorine and fluorine, and with alkoxy groups.
  • substituted alkyl groups include butyoxycthyl, 2-chloroethyl. 2-fluoroethyl, etc.
  • aryl groups which can be present in the phosphorus esters include phenyl, xylyl, cresyl and halogenated phenyl .
  • Phosphates suitable in the present invention include, dipotassium phosphate, disodium phosphate, monopotassium phosphate, tripotassium phosphate, monosodium phosphate, trisodium phosphate, mixtures thereof and the like. Any compatible salt may be used including sodium, potassium, lithium, and the like.
  • the most preferred phosphate is a dipotassium phosphate.
  • the phosphates are preferably present in a fifty percent solution.
  • Phosphates serve to buffer and inhibit corrosion in the formulations of the present invention.
  • the phosphate is preferably present in the formulation as fifty percent dipotassium phosphate in an amount of about 0.1 to about 10.0 percent by weight, and more preferably in an amount of about 1.0 to about 4.0 percent by weight.
  • the phosphonate and sulfonate siloxane-silicate copolymers can be formed in situ upon combination of a water-soluble silicate and a water-soluble siloxane.
  • the silicone-silicate copolymer is selected from the group comprising alkali siliconate silylalkylphosphonates and salts thereof, arylalkyl silicone sulfonate-silicates and salts thereof, and sulfosiloxane-silicates and salts thereof and/or mixtures thereof. These copolymers are believed to provide improved metal corrosion inhibition over the use of the water-soluble silicates.
  • the stabilized silicate is selected from the group comprising alkali siliconate silylalkylphosphonates and salts thereof, arylalkyl silicone sulfonate-silicates and salts thereof, and sulfosiloxane-silicates and salts thereof and/or mixtures thereof.
  • siloxane copolymers substantially inhibit the gelation tendency of a water-soluble silicate at a pH of about 7 to about 11.
  • the anticorrosive activity of the soluble silicate is maintained in the copolymer as compared to an ordinary unstabilized soluble silicate such as sodium silicate.
  • the stabilized silicone/silicate technology is disclosed in U.S. Patents 4,370,255; 4,362,644; and 4,354,002, all hereby incorporated by reference.
  • Other siloxane-silicate copolymers can be utilized in combination with the water- soluble molybdates and the water-soluble salts and esters of phosphorus acids. These are disclosed in U.S. Patent Nos. 3,341,469; 3,337,496; 3,312,622; 3,198,820; 3,203,969; 3,248,329; and 4,093,641 all incorporated herein by reference.
  • Silicone/silicates are used to inhibit corrosion in the formulation of the present invention.
  • the silicone silicates are preferably present in the formulation in an amount of about 0.1 to about 10.0 percent by weight, and more preferably in an amount of about 0.2 to about 1.0 percent by weight .
  • Suitable defoamers include, for example, PLURONIC ® L-61 non-ionic surfactant (commercially available from BASF ®
  • the defoamer may be present in an amount up to about 10.0 percent by weight and more preferably present in an amount of about
  • additives such as bittering agents, dyes, buffering agents, or biocides may be added to the antifreeze/coolant solution.
  • siloxane selected polycarboxylates and stabilized silicates
  • inhibitors are particularly suited for the corrosion protection of aluminum in contact with an aqueous system so as to provide protection against cavitation-erosion corrosion or aluminum water pumps in a long life antifreeze composition providing additional protection as compared to other silicate and stabilized silicate based compositions without the addition of polycarboxylates .
  • Other corrosion inhibitors are optionally added to the aqueous liquid exhibiting synergy together and in combination with the siloxane polycarboxylate components.
  • the synergistic combination of corrosion inhibitors useful in inhibiting the cavitation-erosion corrosion of aluminum water pumps is generally effective in a basic aqueous corrosive media.
  • the corrosion inhibitors of the invention are useful in aqueous alcohol based antifreeze compositions which are generally maintained at a pH of at least 6, and preferably about 7 to about 11.
  • the corrosion inhibitors of the invention are also useful in best transfer media utilized in cooling towers.
  • the antifreeze concentrates of the invention are prepared by first dissolving in a water-alcohol blend
  • an alkali metal azole such as potassium mercaptobenozthiozole or sodium tolyltriazole is then generally added as a 50 percent aqueous solution.
  • an antifoam agent which can be a low-foaming polyoxyethylene adduct of a polyoxypropylene hydrophobic base having a molecular weight of about 1750 wherein the oxycthylene content is about 10 weight percent of the molecule.
  • Additional low- foaming nonionic surface active agents can be used which are disclosed in U.S. Pat. Nos. 3,340,309; 3,504,041; 3,770,701; and 2.425,755. The disclosures of low-foaming nonionic surface active agents in the above-mentioned U.S. patents are incorporated herein by reference.
  • the resultant antifreeze concentrate composition can be diluted with water in accordance with prior a practice to produce an antifreeze fluid or heat transfer medium having be desired freezing point.
  • the antifreeze concentrate used to prepare the coolant can be diluted with about 1 to about 3 volume of water to arrive at the coolant fluid which is circulated in the engine cooling system or in a cooling tower. Smaller or larger quantities of water can be added as necessary to void the freezing of the coolant.
  • ASTM D-1384-87 test was used to evaluate the corrosion inhibitor formulations of the present invention.
  • ASTM D-1384-87 is the standard test method for corrosion testing of engine coolants in glassware and simulates the some world operating conditions of cooling systems.
  • the ASTM D-2570 test was used to evaluate the corrosion inhibitor formulations of the present invention.
  • ASTM D-2570 is the standard test method for simulated service testing of engine coolants in glassware and better simulates the real world operating conditions of cooling systems than the D-1384-87 test.
  • composition A without polycarboxylate
  • Composition B with GOOD-RITE ® K752 polycarboxylate
  • the temperature, test duration, and metal specimen cleaning procedures were all conducted according to ASTM D-1384-87 specifications. All weight changes are in milligrams per specimen (mg/specimen) . A negative weight loss is a weight gain. The passing specification refers to weight loss.
  • compositions A and B were tested which showed the corrosion rate of compositions A and B in mg/cm-cm/week as follows
  • Tables 1-4 show the percent silicate in solution for Composition A (without the polycarboxylate) vs Composition B (with GOOD-RITE ® 752 polycarboxylate) as a function of the addition of the polycarboxylate, specifically the GOOD-RITE ® K752 in combination with the stabilized siloxane silicate and other synergistically acting components including the water soluble nitrate and nitrites, water soluble phosphates, azole compound, water soluble molybdate, sodiu hydroxide in the glycol solution
  • the silicate level drops precipitously for Composition A without the selected polycarboxylate additive
  • composition B containing the selected GOOD RITE ® K752 polycarboxylate and stabilized silicate "siloxane” compound would show a relatively constant rate of depletion for silicate, yet a sufficient amount of silicate s maintained in solution for the duration of the test

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Abstract

The present invention provides heavy duty long life corrosion inhibition formulations and compositions for inhibiting mineral scale and the corrosion of metals particularly the cavitation corrosion of aluminum in the presence of aqueous liquids. The combination of a mixture of polymeric polycarboxylates, azoles, a combination of nitrite and nitrate salts, phosphates, stabilized silicates and transition metal compounds provide a synergistic protective effect against the cavitation corrosion of aluminum in aqueous liquids reducing the corrosion rate and is effective at relatively low concentrations and varying pH ranges. The addition of selected polymeric polycarboxylates not only significantly reduces glycol based coolant cavitation erosion-corrosion, heat rejecting aluminum corrosion, and hard water precipitates and scale, it has been discovered that polymeric polycarboxylates in combination with siloxane stabilized silicates enhance secondary silicate stabilization leading to improvement in an aluminum corrosion protection and coolant life when utilized with selected amounts of the above-identified additives. The formulations are particularly suitable for automotive applications.

Description

TITLE: DIESEL ENGINE ANTIFREEZE COMPOSITION
TECHNICAL FIELD
This invention relates to extending diesel engine coolant lifetime through polymeric polycarboxylate secondary silicate stabilization. More particulary, this invention relates to an antifreeze formulation for inhibition and prevention erosion and corrosion of aluminum and the corrosion of other metals exposed to an aqueous liquid in automotive coolant systems. The formulation further inhibits mineral scale.
The novel antifreeze formulation comprises a mixture of polymeric polycarboxylates, azoles, nitrate and nitrite salts, phosphates, siloxane stabilized silicates and transition metal compounds which provide a synergistic protective effect against the cavitation corrosion of aluminum in aqueous liquids reducing the corrosion rate and is effective at relatively low concentrations and varying pH ranges . The addition of selected polymeric polycarboxylates not only significantly reduces glycol based coolant cavitation erosion-corrosion, heat rejecting aluminum corrosion, and hard water precipitates and scale, it has been discovered that selected polymeric polycarboxylates in combination with siloxane stabilized silicates enhance secondary silicate stabilization leading to improvement in aluminum corrosion protection and coolant life when utilized with selected amounts of the above- identified additives. The formulations are particularly suitable for automotive applications .
DESCRIPTION OF THE PRIOR ART
Antifreeze/coolant technology traditionally use silicate as a corrosion inhibitor. Silicates are particularly useful in protecting aluminum automotive cooling system components. The silicate corrosion inhibitors generally also use a phosphate, usually in the form of an alkali metal salt, to help protect metal cooling system parts and also as a buffer to control the pH of the coolant. Often phosphate salts are used to help maintain a stable alkaline environment from which multiple corrosion inhibitors can most effectively function.
Traditionally antifreeze/coolant is sold at nearly one-hundred percent glycol content. This concentrated packaging allows for flexibility so that the user can dilute the antifreeze/coolant, as needed, with available water to obtain the required freeze/boil protection. However, corrosion protection is needed over the entire dilution range. In modern automotive engineering, many engine components are fabricated from aluminum. Engine coolants, primarily ethylene glycol or propylene glycol based solutions, must transfer heat from operating aluminum engines while inhibiting corrosion. Older automotive engines did not have aluminum components and thus, the traditional antifreeze/coolant compositions may produce corrosion in heat rejecting aluminum or aluminum alloy components. The cavitation erosion-corrosion of aluminum water pumps upon exposure to aqueous systems such as water-cooled internal combustion engine coolants is a relatively new development.
U.S. Patent 4,717,495 by Hercamp et al . , hereby incorporated by reference, teaches a sodium-free buffer solution. U.S. Patent No. 4,548,787 discloses the use of a combination water soluble phosphate with tungstae, selenate and molybdate for protection against cavitation erosion-corrosion on aluminum. U.S. Patent No. 4,404113 discloses the use of polyhydric alcohols as corrosion inhibiting and cavitation reducing additives for coolants.
Certain polycarboxylate type materials have been disclosed for prevention of precipitates in antifreeze/coolant compositions. for example, U.S. Patent No. 3,663,448 discloses scale inhibition for industrial cooling waters using amino phosphonate and polyacrylic acid compounds, U.S. Patent No. 3,948,792 discloses an aqueous additive mixture to reduce and modify the amount of silicate scale formed in automotive cooling systems.
U.S. Patent No 4,487,712 discloses the use of polyacrylic acid as a silicate stabilizer to inhibit gelation which is a silicate depletion mechanism which can occur separately from hard water precipitates.
The addition of polymeric polycarboxylates has been shown to significantly reduce glycol based coolant cavitation erosion- corrosion as set forth in U.S. Patent Nos. 5,288,419 and 5,290,469; to reduce heat rejecting aluminum corrosion as set forth in U.S. Patent Nos. 5,320,670 and 5,290,467; and to reduce hard water precipitates and scale as set forth in U.S. Patent Nos. 5,330,670 and 5,290,468; all of which are hereby incorporated by reference.
U.S. Patent No. 4,440,721, hereby incorporated by reference, discloses the combination of a water-soluble phosphate with a water soluble molybdate, tungstate, or selenate for providing a protective effect against the cavitation corrosion of aluminum in aqueous liquids. While alkali metal molybdates and the soluble salts of tungstic and selenic acids have been used in antifreeze compositions to prevent the corrosion of metals, particularly cast iron, soluble salts of molybdic, tungstic and selenic acids act to retard the corrosion of aluminum, particularly the cavitation erosion-corrosion of aluminum water pumps .
None of the above references provide a means for obtaining a long life silicate based antifreeze composition as does Applicant's present invention. The combination of a selected polymeric polycarboxylates, azoles, nitrate and nitrite salts, molybdates, phosphates, stabilized silicates and transition metal compounds provide a synergistic protective effect against the cavitation corrosion of aluminum in aqueous liquids reducing the corrosion rate and is effective at relatively low concentrations and varying pH ranges. The addition of selected polymeric polycarboxylates not only significantly reduces glycol based coolant cavitation erosion-corrosion, heat rejecting aluminum corrosion, and hard water precipitates and scale, it has been discovered that utilization of selected polymeric polycarboxylates in combination with certain additives enhance secondary silicate stabilization leading to improvement in aluminum corrosion protection and coolant life.
Moreover, such a formulation would be designed for modern aluminum engine based passenger car cooling systems. The formulation must be liquid, easily miscible with diluted antifreeze in the cooling system, protect all cooling system metals, have a useful shelf life, not harm automotive finishes or paint and not promote excessive cooling system foam.
SUMMARY OF THE INVENTION
The present invention has met the above-described need by providing an antifreeze/coolant composition using selected polymeric polycarboxylate additives which reduce corrosion over the entire dilution range without creating precipitates. This composition is soluble in water, alcohol, and alcohol/water mixtures, is compatible with other commonly used antifreeze/coolant components, does not corrode or damage automotive cooling systems and is effective at relatively low concentrations. In addition, the present corrosion inhibition formulations are effective in reducing corrosion in the entire range of cooling system metals, including heat rejecting aluminum, aluminum alloys, copper, steel, cast iron, brass, solder and the like. It his been found that water-soluble salts of an acid elected from the group consisting or molybdic, tungstic and selenic acids or salts thereof, in combination with a water-soluble phosphate and a polymeric polycarboxylate provide a synergistic improvement in the retardation or the cavitation erosion- corrosion of aluminum water pumps and other metal engine components when used in contact with aqueous liquids, particularly aqueous antifreeze compositions containing a water-soluble alcohol freezing point depressant.
It is an object of the present invention to provide corrosion inhibition formulations for antifreeze/coolant compositions with selected polymeric polycarboxylate additives for reducing glycol based coolant cavitation erosion-corrosion.
It is another object of the present invention to provide corrosion inhibition formulations for antifreeze/coolant compositions with selected polymeric polycarboxylate additives for enhancing silicate stability providing an improvement in coolant life.
It is another object of the present invention to provide corrosion inhibition formulations which reduce corrosion over the entire dilution range of antifreeze/coolant compositions without creating precipitates.
It is an additional object of the present invention to provide corrosion inhibition formulations which are effective in reducing corrosion in the entire range of cooling system metals. It is an additional object of the present invention to provide corrosion inhibition formulations which are effective in reducing heat rejecting aluminum corrosion.
It is an additional object of the present invention to provide corrosion inhibition formulations which are effective in reducing hard water precipitates and scale. It is a further object of the present invention to provide corrosion inhibition formulations which are soluble in alcohol, alcohol/water mixtures and water alone. It is an object of the present invention to provide corrosion inhibition formulations which are compatible with commonly used antifreeze/coolant components.
It is another object of the present invention to provide corrosion inhibition formulations which are effective at relatively low concentrations.
It is an additional object of the present invention to use polymeric polycarboxylates in the corrosion inhibition formulations to reduce the corrosion.
It is a further object of the present invention to utilize a combination of nitrites and nitrates to maximize the protection of ferrous metals and minimize pitting thereof .
It is a further object of the present invention to utilize molybdate to protect against erosion and cavitation of aluminum.
These and other objects of the present invention will be more fully understood from the following description of the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The present invention provides long life corrosion inhibition antifreeze/coolant compositions by using certain polymeric polycarboxylate additives in a synergistic combination with stabilized silicate
("siloxane") , and other selected compounds, primarily the combination of nitrates and nitrates and an increased amount of molybdate which reduces coolant cavitation erosion-corrosion, heat rejecting aluminum corrosion, and hard water precipitates and scale. Moreover, it has been discovered that polymeric polycarboxylates enhance secondary silicate stabilization leading to improvement in aluminum corrosion protection and prolonged coolant life as compared to conventional silicon based coolants. In addition, the present corrosion inhibition formulations are effective in reducing corrosion in the entire range of cooling system metals, including heat rejecting aluminum, aluminum alloys, copper, steel, cast iron, brass, solder and the like. This formulation is soluble in alcohol, alcohol/water mixtures and in water alone and exhibits excellent stability characteristics. The most preferred antifreeze/coolant composition is a silicate-phosphate type having a pH of about 10.5 and having about 94% antifreeze grade glycols and about 3% corrosion inhibitors, with the balance being water.
The freezing point depressant utilized in the antifreeze compositions of the invention can be any suitable water-soluble liquid alcohol used heretofore in formulating antifreeze compositions. The water-soluble alcohol contains 1 to about 4 carbon atoms and 1 to about 3 hydroxy groups . Ethylene glycol is preferred as the freezing point depressant and especially the commercially available mixtures containing largely ethylene glycol and a small amount of diethylene glycol . The commercial mixture generally contains at least 85 to 95 percent by weight of ethylene glycol with the remainder being diethylene glycol and small amounts of substances which are incidentally present such as water. Other water- soluble liquid alcohol can be admixed with ethylene glycol but such mixtures usually are not preferred. Inexpensive commercially available water soluble alcohols can also be used such as methyl, ethyl, propyl, and isopropyl alcohol alone or in mixtures .
The concentrated corrosion inhibitor formulations of the present invention is a water-based mixture of polymeric polycarboxylates, nitrate and nitrite salts, molybdates, phosphate, azoles, stabilized silicates and transition metal compounds . Optionally, other components including defoamers, dyes, buffering agents, biocides, detergents, and the like may be added to the present formulation. Although a water soluble phosphate level is given on the basis of hydrogen phosphate, alkali metal salts are typically used. Alkaline earth or ammonium slats are also possible alone or in combination therewith. Nitrates and nitrites are typically introduced as an alkali salt although acid, alkaline earth or ammonium salts could be utilized including potassium, sodium or salts alone or in combinations therewith. The azoles include tolytriazole, benzotriazole, mercaptobenzothizole including mixtures and other substituted azoles. Stabilized silicate, typically referred to as siloxane compounds, are of the type described in U.S. Patent Nos. 4,354,002, 4,362,644, and/or 4,370,255, hereby incorporated by reference. Suitable defoamers include PLURONIC® L-61, PATCOTE® 415 and other surfactants including silicone types. The synergistic combination of phosphate, molybdate and stabilized silicate is described in U.S. Patent Nos. 4,548,787, 4,707,286, and 4 , 440 , 721 , hereby incorporated by reference.
It is contemplated that in addition to silicate- phosphate type coolants, these additives are useful in silicate-borax, silicate phosphate and borax coolants, organic acid, and organic acid silicate hybrid type coolants, and the like. The corrosion inhibitor formulations are compatible with other commonly used antifreeze/coolant components and are effective at relatively low concentrations. Each of the preferred ingredients of the synergistic antifreeze formulation, whether mandatory or optional, is discussed below:
POLYCARBOXYLATES
The preferred class of stabilizing polymeric polycarboxylates are based on polyacrylic acid (PAA) and/or polymaleic acid (PMA) . These polymeric polycarboxylates are compatible with other components in the typical antifreeze/coolant composition, and present no additional toxicity or disposal concerns . The molecular weight distribution of useful materials may average about one hundred grams/mole to about three million grams/mole. Chemically, the materials should be based on polymers and copolymers of acrylic acid and/or maleic acid, including any modifiers, such as alcohols. The polycarboxylates used in the present invention have a molecular weight range of from about 1,200 to about 250,000, with a preferred range of from 500 to 12,000. More specifically, the most preferred additives have average molecular weights in the range of about 500 to about 4,000, and more specifically about 1300 to about 1800 and about 300 to about 4600.
When reference is made to polycarboxylates within the context of the present invention it is understood to encompass those watersoluble homo- and copolymers having at least one monomeric unit containing C3-6 monoethylenically unsaturated mono- or dicarboxylic acids or their salts. Suitable monocarboxylic acids of this type are for example, acrylic acid, methacrylic acid, ethacrylic acid, vinylacetic acid, allylacetic acid, and crotonic acid. The preferable monocarboxylic acids from this group are acrylic acid and methacrylic acid. A further component of the polycarboxylate comprises monoethylenically unsaturated C4-s dicarboxylic acids, for example, maleic acid, itaconic acid, citraconic acid, mesaconic acid, fumaric acid, or methylenemalonic acid. The preferred acid is maleic acid.
Other organic substituents may be used as co- monomers or as modifiers added along the polymer chain. Examples of such are shown as Formula I . H R
C-C (I)
H X n where R=H or a secondary alcohol such as isopropanol, X=COOH, COONa÷, ethylvinylether, isobutylene, vinyl acetate, acrylamide, or styrene, with the proviso that when R= a secondary alcohol, X=COOH or COO-Na+, and when X= any other above referenced group, R=H. The preferred polycarboxylates are a copolymer of acrylic acid and maleic acid, or their sodium salts, said copolymer having a molecular weight of 3000, and a sodium salt of polyacrylic acid modified with a secondary alcohol such as isopropanol, said polymer having a molecular weight of 4000.
The polycarboxylates used in the present invention are obtained by methods well known to those skilled in the art. The general method of synthesis is via free acid radical polymerization. The polymerization may be carried out in an aqueous medium, in the presence of polymerization initiators, with or without regulants. The polymerization can take various forms,- for example, the monomer (s) can be polymerized batchwise in the form of aqueous solutions. It is also possible to introduce into the polymerization reactor a portion of the monomer (s) and a portion of the initiator, to heat the mixture in an inert atmosphere to the polymerization temperature and then to add the remaining monomer (s) and initiator to the reactor at the rate of polymerization.
Polymerization temperatures range from 20°C to 200°C. At temperatures above 100°C, pressure vessels are employed.
The carboxyl containing monomers can be polymerized in the free carboxylic acid form, in the partial neutralized form, or completely neutralized. The neutralization is preferably effected with alkali metal or ammonium base .
The polymerization initiators used are preferably water soluble free radical formers such as hydrogen peroxide, peroxodisulfates and mixtures of the two. The polymerization may also be started with water insoluble initiators such as dibenzoyl peroxide, dilaurylperoxide, or azodiisobutyronitrile . The polymerization may be carried out in the presence of regulants . Examples of such regulants include water soluble mercaptans, ammonium formate, and hydroxylammonium sulfate. Polymeric polycarboxylate materials which are useful in the present invention include Belclene water treatment additives from CIBA-GEIGY®, Colloid additives from COLLOIDS®, Inc., GOOD-RITE® polyacrylates and CARBOPOL® resins from BF GOODRICH® and the like. Examples of the polycarboxylates which may be used in the present invention are those marketed by BASF® under the trademark SOKALAN® polycarboxylates, which are available in aqueous polymer solutions . More particularly, the SOKALAN® polyacrylic dispersants are copolymer carboxylate dispersants. These SOKALAN® polycarboxylates are acrylic/maleic copolymers and other copolymers of either maleic or acrylic acid. These polycarboxylates are generally fully neutralized. The suffix "S" is a designation used to indicate free acids in the SOKALAN® range.
While particularly preferred additive, SOKALAN® CP10, CPlOs, or CP12s, has been shown to be particularly effective at about 0.05 to about 0.20 weight percent in one inhibitor concentrate, other levels of additive and different polycarboxylates may also be used. SOKALAN® 10 has an average relative molecular weight of about 4,000, and comprises a secondary alcohol modified polyacrylic acids; whereas SOKALAN® 12 has an average relative molecular weight of about 3,000 and comprises a sodium salt of a copolymer of acrylic acid and maleic acid. The polymeric polycarboxylate is preferably present in the formulation in an amount of about 0.001 to about 10.0 percent by weight, and more preferably in an amount of about 0.01 to about 0.1 percent by weight. The polymeric polycarboxylate is effective at enhancing stability at relatively low concentrations, generally about 100 to about 1000 ppm per total volume of inhibitor concentrate. The most preferred polycarboxylates are the K-700 polyacrylate polymers from BF GOODRICH® which include the GOOD-RITE® K-732 AND GOOD-RITE® K-752 polyacrylate polymers . Both are mixtures of sodium polyacrylate and polyacrylic acid in water as set forth and described in the copies of the Material Safety Data sheets as set forth in the Information Disclosure Document and incorporated by reference herewith. These polymers are similar, while differentiated by their molecular weight.
The GOOD-RITE® K-752 polyacrylate is a water soluble acrylic acid polymer supplied as a clear to hazy, colorless to amber colored, and ranging from about 62% to about 64% total solids solution in water averaging about 63%, with the active solids being about 62.5% having a specific gravity of about 1.23. The molecular weight (GPC Mκ) is about 2100. The pH ranges from about 2.2 to 3.0 and averages about 2.6. Viscosity (CP at 25°C) ranges from between about 400 to about 1,400, and averages about 950. The GOOD-RITE® K-732 polyacrylate is a water soluble acrylic acid polymer supplied as a clear to hazy, colorless to amber colored, and ranging from about 49% to about 51% total solids solution in water and averaging about 50%, with the active solids being about 49.5% having a specific gravity of about 1.2. The molecular weight (GPC Mw) is about 5,100. The pH ranges from about 2.2 to 3.0 and averages about 2.6. Viscosity (CP at 25°C) ranges from between about 250 to about 500, and averages about 350. Combinations of the polycarboxylates may also be utilized in the present invention such as a mixture of a secondary alcohol modified polyacrylic acid, a sodium salt of a copolymer of acrylic acid and maleic acid and/or mixtures of sodium polyacrylate and polyacrylic acid in water. These combinations having a molecular weight of less than 10,000 are deemed to be suitable polycarboxylate additives .
SALT CORROSION INHIBITORS (Nitrates and Nitrites)
Where the aqueous liquids contact other metals in addition to aluminum, including aluminum water pumps, metal salt corrosion inhibitors, preferably alkali metal salts known in the prior art can be usefully added to the aqueous liquids or the invention. Such known corrosion inhibitors include the water-soluble: nitrates, nitrites, silicates, carbonates, sodium silicate, sodium nitrate, potassium carbonate, ammonium silicate.
Preferably, a nitrate in combination with a nitrite is used in the preferred composition in a higher concentration for heavy duty applications in diesel engines than typically used in gasoline engines. The source of the nitrate and nitrite ions can be any water- soluble nitrate or nitrite such as the alkali metal nitrates and nitrites . Nitrate salts suitable in the present invention include, sodium nitrate, potassium nitrate, magnesium nitrate, calcium nitrate, lithium nitrate, mixtures thereof and the like. Nitrite salts suitable in the present invention include, sodium nitrite, potassium nitrite, magnesium nitrite, calcium nitrite, lithium nitrite, mixtures thereof and the like. Any compatible salt may be used including sodium, potassium, lithium, magnesium, calcium and the like. The most preferred nitrate salt is sodium nitrate and the preferred nitrite is sodium nitrite.
Other equivalent methods of supplying nitrate may be used. For example, the pH of the total composition may be adjusted by addition of nitric acid ions. The reaction of nitrate acid and basic salts contained in the composition will result in liberation of free carboxylic acid and the formation of nitrate salts .
Nitrate salts serve to inhibit corrosion in the formulations of the present invention and aids in the protection of aluminum. The nitrate salt is preferably present in the formulation in an amount of about 0.01 to about 10.0 percent by weight, more preferably in an amount of about 0.1 to about 3.0 percent by weight, and most preferably in an amount of about 0.1 to about 1.0 percent by weight . Nitrite salts are especially good for preventing heavy duty cylinder linings from pitting. They are good oxidizers when used with ferrous metals for protecting surfaces such as cylinder liner sleeves and other ferrous components of diesel engines. The nitrites have a higher oxidation state than the nitrates and are ions are depleted at a higher rate making them more expensive than the nitrate salts,- however, the nitrites are especially good in reducing pitting by forming a coating on the ferrous surface. Of course, the nitrates form nitrites upon oxidation. The nitrite salt is preferably present in the formulation in an amount of about 0.01 to about 10.0 percent by weight, more preferably in an amount of about 0.1 to about 3.0 percent by weight, and more preferably in an amount of about 0.1 to about 1.0 percent by weight.
The preferred embodiment of the present formulation utilizes a greater amount of water soluble nitrite than water soluble nitrates. More specifically, one preferred formula utilizes water soluble nitrates in a range of from about 0.05 to about 0.30 percent by weight, and water soluble nitrites in a range of from about 0.30 to about 0.60 percent by weight, representing about a 2:1 ratio. AZOLE ADDITIVES
Azoles are present in the formulation to inhibit corrosion of yellow metal like copper and brass. Brass thermostats and radiator caps are common as well as copper and brass radiators. The azole compound providing protection for copper and brass from corrosion is selected from among the water- soluble triazoles, pyrazoles, imidazoles, isooxazoles, isothiazoles, thiazoles, thiadiazole salts, and the like. Generally, the alkali metal salts are used. Specific preferred azole compounds include 1, 2, 3 -benzotriazole; 1, 2, 3 -tolyltriazole,- sodium 2 -mercaptobenzothiazole; and sodium 2-mercaptobenzimidazole . Azole compounds suitable in the present invention include, salts of mercaptobenzothiazole, salts of tolytriazole, benzotriazole, mixtures thereof and the like. Typically, these azoles are preferably present in a fifty percent concentration. However, one preferred azole compound consists of the salts of mercaptobenzothiazole and salts of tolytriazole. More particularly, one preferred azole compound is a mixture of sodium mercaptobenzothiazole and sodium tolytriazole which may be used in about a 3 to 1 ratio.
The azoles are preferably present in the ormulation in an amount of about 0.01 to about 10.0 percent by weight, and more preferably in an amount of about 0.05 to about 1.0 percent by weight. Generally, the azole compound is used in amounts of about 0.1 parts to about 0.5 parts by weight, preferably about 0.1 to about 0.4 parts by weight, based on 100 parts by weight of the aqueous liquid. MOLYBDATE ADDITIVES
The water-soluble molybdate which is preferred for use in the aqueous systems of the present invention can be any salt of molybdic acid which is readily soluble in water. These include both alkali metal and alkaline earth metal molybdates as well as ammonium molybdate, the term "alkali molybdate" being used in a broad sense so as to include alkali metal, alkaline earth metal and ammonium molybdates . Examples of useful molybdates are sodium molybdate . potassium molybdate, lithium molybdate and ammonium molybdates including ammonium dimolybdate and ammonium heptamolybdate . Alkali molybdate compounds, sodium molybdate and potassium molybdate are preferred because of their availability and compatibility with the aqueous system as well as for economic reasons . The specific concentration of the molybdate ion will vary depending upon the degree of hardness of the aqueous system, the temperature, and the amount of dissolved oxygen in the aqueous system. While concentrations of the molybdate ion above about 0.5 parts by weight per 100 parts by weight of aqueous liquid can be employed, in most instances concentrations of molybdate ion above this limit normally do not provide significant improvements in the inhibitive characteristics or the aqueous system and are undesirable for economic reasons.
Transition metal compounds suitable for use in the present invention include, disodium salt dehydrate of molybdic acid, sodium molybdate 2H20, molybdenum trioxide, silicoheteropolymolybdates, phosphoroheteropolymolybdates, mixtures thereof and the like. Any compatible transition metal may be used, including for example, molybdate, cobalt, cerium, mixtures thereof and the like. In addition, any acid salt may be used including sodium, potassium, lithium, calcium, magnesium and the like. The most preferred transition metal compound is the disodium salt dehydrate of molybdic acid or sodium molybdate 2H20.
Transition metal acids are used to inhibit corrosion in formulations of the present invention. The transition metal compound is preferably present in the formulation in an amount of about 0.001 to about 10.0 percent by weight, and more preferably in an amount of about 0.1 to about 0.5 percent by weight. The molybdate ion is employed in amounts so as to provide a concentration in the aqueous system of at least about 0.01 parts by weight per 100 parts by weight of aqueous liquid. Preferably about 0.15 to about 0.2 parts by weight per 100 parts by weight of molybdate based upon said aqueous liquid are employed. More molybdate is utilized in the present diesel engine formulation than typically used in automotive engine coolants.
PHOSPHORUS ADDITIVES
Both inorganic and organic water-soluble phosphorus compounds are useful in inhibiting the cavitation erosion corrosion of aluminum in contact with aqueous liquids. The water-soluble phosphates are used generally in amounts so as to provide a concentration of about 0.5 to about 2 parts by weight per 100 parts by weight of the aqueous liquid. These compounds include the preferred water-soluble alkali metal salts of orthophosphoric acid, pyrophosphoric acid, and metaphosphoric acid. Orthophosphoric acid being tri-basic forms three series of salts, potassium dihydrogen phosphate, disodium hydrogen phosphate, and trisodium phosphate. Useful organic phosphates include the oxyesters of phosphoric acid, as well as the amides and triesters thereof. The most common phosphorus acid esters which are useful are the mono-, di-, and tri-esters of orthophosphoric acid. These can be alkyl phosphates , aryl phosphates and mixed alkyl-aryl phosphates. Representative alkyl groups having 1 to about 18 carbon atoms which can be present in the alkyl phosphates include methyl, ethyl, propyl, isopropyl and n-butyl, isobutyl, etc. Representative substituted alkyl groups which can be present in the phosphorus esters include said alkyl groups substituted with halogen, especially chlorine and fluorine, and with alkoxy groups. Examples of substituted alkyl groups include butoxyethyl, 2-chloroethyl, 2-nuoroethyl, etc. Examples or other groups which can be present in the phosphorus esters include alkyl groups substituted with halogen, especially chlorine and fluorine, and with alkoxy groups. Examples of substituted alkyl groups include butyoxycthyl, 2-chloroethyl. 2-fluoroethyl, etc. Examples of aryl groups which can be present in the phosphorus esters include phenyl, xylyl, cresyl and halogenated phenyl .
Phosphates suitable in the present invention include, dipotassium phosphate, disodium phosphate, monopotassium phosphate, tripotassium phosphate, monosodium phosphate, trisodium phosphate, mixtures thereof and the like. Any compatible salt may be used including sodium, potassium, lithium, and the like. The most preferred phosphate is a dipotassium phosphate. The phosphates are preferably present in a fifty percent solution.
Phosphates serve to buffer and inhibit corrosion in the formulations of the present invention. The phosphate is preferably present in the formulation as fifty percent dipotassium phosphate in an amount of about 0.1 to about 10.0 percent by weight, and more preferably in an amount of about 1.0 to about 4.0 percent by weight.
SILOXANE-SILICATE COPOLYMERS
The phosphonate and sulfonate siloxane-silicate copolymers can be formed in situ upon combination of a water-soluble silicate and a water-soluble siloxane. In the preferred composition, the silicone-silicate copolymer is selected from the group comprising alkali siliconate silylalkylphosphonates and salts thereof, arylalkyl silicone sulfonate-silicates and salts thereof, and sulfosiloxane-silicates and salts thereof and/or mixtures thereof. These copolymers are believed to provide improved metal corrosion inhibition over the use of the water-soluble silicates. The stabilized silicate,
("siloxane copolymers"), substantially inhibit the gelation tendency of a water-soluble silicate at a pH of about 7 to about 11. The anticorrosive activity of the soluble silicate is maintained in the copolymer as compared to an ordinary unstabilized soluble silicate such as sodium silicate. The stabilized silicone/silicate technology is disclosed in U.S. Patents 4,370,255; 4,362,644; and 4,354,002, all hereby incorporated by reference. Other siloxane-silicate copolymers can be utilized in combination with the water- soluble molybdates and the water-soluble salts and esters of phosphorus acids. These are disclosed in U.S. Patent Nos. 3,341,469; 3,337,496; 3,312,622; 3,198,820; 3,203,969; 3,248,329; and 4,093,641 all incorporated herein by reference.
Silicone/silicates are used to inhibit corrosion in the formulation of the present invention. The silicone silicates are preferably present in the formulation in an amount of about 0.1 to about 10.0 percent by weight, and more preferably in an amount of about 0.2 to about 1.0 percent by weight .
DEFOAMERS
Any suitable defoamer, well known in the art, is suitable for the present formulations . Suitable defoamers include, for example, PLURONIC® L-61 non-ionic surfactant (commercially available from BASF®
Corporation) or PATCOTE® 415 liquid defoamer
(commercially available from Patco Specialty Chemicals Division, American Ingredients Company) . The defoamer may be present in an amount up to about 10.0 percent by weight and more preferably present in an amount of about
0.001 to about 10.0 percent by weight, and most preferably, in an amount of about 0.01 to about 0.05 percent by weight.
ADDITIVES
Other additives such as bittering agents, dyes, buffering agents, or biocides may be added to the antifreeze/coolant solution.
Synergistic Effect
The above synergistic combination of selected polycarboxylates and stabilized silicates ("siloxane"), in combination with inhibitors is particularly suited for the corrosion protection of aluminum in contact with an aqueous system so as to provide protection against cavitation-erosion corrosion or aluminum water pumps in a long life antifreeze composition providing additional protection as compared to other silicate and stabilized silicate based compositions without the addition of polycarboxylates . Other corrosion inhibitors are optionally added to the aqueous liquid exhibiting synergy together and in combination with the siloxane polycarboxylate components.
The synergistic combination of corrosion inhibitors useful in inhibiting the cavitation-erosion corrosion of aluminum water pumps is generally effective in a basic aqueous corrosive media. For instance, the corrosion inhibitors of the invention are useful in aqueous alcohol based antifreeze compositions which are generally maintained at a pH of at least 6, and preferably about 7 to about 11. The corrosion inhibitors of the invention are also useful in best transfer media utilized in cooling towers.
The antifreeze concentrates of the invention are prepared by first dissolving in a water-alcohol blend
(preferably ethylene glycol in combination with diethylene glycol) a water-soluble silicate, an organosiloxane, preferably a phosphonate siloxane, or a sulfonate siloxane, and an alkali metal molybdate, tungstate or selenate. Subsequently the composition is rendered basic by the addition of sodium or potassium hydroxide. Where protection against the corrosion of copper and copper-containing alloys is also required in addition to aluminum in contact with the aqueous antifreeze concentrates of the invention, an alkali metal azole such as potassium mercaptobenozthiozole or sodium tolyltriazole is then generally added as a 50 percent aqueous solution. Optionally, an antifoam agent is used which can be a low-foaming polyoxyethylene adduct of a polyoxypropylene hydrophobic base having a molecular weight of about 1750 wherein the oxycthylene content is about 10 weight percent of the molecule. Additional low- foaming nonionic surface active agents can be used which are disclosed in U.S. Pat. Nos. 3,340,309; 3,504,041; 3,770,701; and 2.425,755. The disclosures of low-foaming nonionic surface active agents in the above-mentioned U.S. patents are incorporated herein by reference. The resultant antifreeze concentrate composition can be diluted with water in accordance with prior a practice to produce an antifreeze fluid or heat transfer medium having be desired freezing point. As a general rule, the antifreeze concentrate used to prepare the coolant can be diluted with about 1 to about 3 volume of water to arrive at the coolant fluid which is circulated in the engine cooling system or in a cooling tower. Smaller or larger quantities of water can be added as necessary to void the freezing of the coolant.
In order to obtain the desired resistance to cavitation erosion corrosion of aluminum water pumps in contact with aqueous liquids containing a siloxane- silicate co-polymer metal corrosion inhibitor, it is necessary to provide the required amounts of phosphate and at least one of a molybdate, tungstate, or selenate in the amounts specified above.
EXPERIMENTAL EVALUATION
The ASTM D-1384-87 test was used to evaluate the corrosion inhibitor formulations of the present invention. ASTM D-1384-87 is the standard test method for corrosion testing of engine coolants in glassware and simulates the some world operating conditions of cooling systems. The ASTM D-2570 test was used to evaluate the corrosion inhibitor formulations of the present invention. ASTM D-2570 is the standard test method for simulated service testing of engine coolants in glassware and better simulates the real world operating conditions of cooling systems than the D-1384-87 test.
A typical formulation utilizing GOODRITE K-752® polycarboxylate as compared to a conventional formula are presented in Table 1. Similar results would be expected substituting SOKALAN® CP-12s polycarboxylate for the GOODRITE K-752®.
TABLE 1
(Formulations)
Composition A (without polycarboxylate) Composition B (with GOOD-RITE® K752 polycarboxylate)
Figure imgf000026_0001
The temperature, test duration, and metal specimen cleaning procedures were all conducted according to ASTM D-1384-87 specifications. All weight changes are in milligrams per specimen (mg/specimen) . A negative weight loss is a weight gain. The passing specification refers to weight loss.
TABLE 2
(ASTM D-1384 Weight Loss in Mg/Specimen)
Figure imgf000027_0001
The results from Table 2 show that Formulations A and B passed the ASTM D-1384 weight loss tests. TABLE 3
Figure imgf000028_0001
The results from Table 3 show that Formulations A and B passed the ASTM D-2570 simulated service weight loss tests
Moreover, an ASTM D-4340 test was conducted which showed the corrosion rate of compositions A and B in mg/cm-cm/week as follows
TABLE 4
Figure imgf000028_0002
Tables 1-4 show the percent silicate in solution for Composition A (without the polycarboxylate) vs Composition B (with GOOD-RITE® 752 polycarboxylate) as a function of the addition of the polycarboxylate, specifically the GOOD-RITE® K752 in combination with the stabilized siloxane silicate and other synergistically acting components including the water soluble nitrate and nitrites, water soluble phosphates, azole compound, water soluble molybdate, sodiu hydroxide in the glycol solution The silicate level drops precipitously for Composition A without the selected polycarboxylate additive
It is expected that Composition B containing the selected GOOD RITE® K752 polycarboxylate and stabilized silicate "siloxane" compound would show a relatively constant rate of depletion for silicate, yet a sufficient amount of silicate s maintained in solution for the duration of the test
The foregoing detailed description is given primarily for clearness of understanding and no unnecessary limitations are to be understood therefrom, for modification will become obvious to those skilled in the art upon reading this disclosure and may be made upon departing from the spirit of the invention and scope of the appended claims Accordingly, this invention is not intended to be limited by the specific exemplifications presented hereinabove Rather, what is intended to be covered is within the spirit and scope of the appended claims

Claims

We claim:
Claim 1 An antifreeze/coolant solution for inhibiting the corrosion of metals and inhibiting mineral scale based on 100 parts by weight of said glycol -based solution, comprising: a polymeric polycarboxylate in the amount of from about 0001 to about 10.0 percent by weight, a salt which is at least one selected from the group consisting of sodium nitrate, potassium nitrate, magnesium nitrate, calcium nitrate, lithium nitrate and combinations thereof in an amount of about 0.01 to about 100 percent by weight; a salt which is at least one selected from the group consisting of sodium nitrite, potassium nitrite, magnesium nitrite, calcium nitrite, lithium nitrite and combinations thereof in an amount of about 0.01 to about 100 percent by weight; an azole compound which is selected from the group consisting essentially of sodium mercaptobenzoth azole, sodium tolytriazole, water-soluble tπ azoles, pyrazoles, imidazoles, isooxazoles, isothiazoles, thiazoles, thiadiazole, 1, 2, 3-benzotπazole, 1,2,3- tolyltπazole, sodium -mercaptobenzothiazole, and sodium 2- mercaptobenzimidazole in an amount of about 0.01 to about 10.0 percent by weight, a silicone-silicate copolymer in an amount of about 0.1 to about 100 percent by weight,; a phosphate compound which is selected from the group consisting essentially of dipotassium phosphate, disodium phosphate, monopotassium phosphate, tπpotassium phosphate, monosodium phosphate, trisodium phosphate, and mixtures thereof in an amount of about 0.1 to about 10.0 percent by weight; a transition metal compound selected from the group consisting essentially of disodium salt dihydrate of molybdic acid, molybdenum trioxide, silicoheteropolymolybdates and/or phosphoroheteropolymolybdates, sodium molybdate, potassium molybdate, lithium molybdate, ammonium molybdate, ammonium dimolybdate, and ammonium heptamolybdate in an amount of about 0.001 to about 10.0 percent by weight; and a glycol compound selected from the group consisting essentially of ethylene glycol , diethylene glycol , propylene glycol , methyl alcohol, ethyl alcohol, propyl alcohol, isopropyl alcohol and combinations thereof making up the balance of the solution.
2. The antifreeze/coolant solution of claim 1, wherein said polymeric polycarboxylate has a molecular weight in a range of between about 500 to 12,000.
3. The antifreeze/coolant solution of claim 1, wherein said polymeric polycarboxylate has a molecular weight in a range of between about 500 to 4,000.
4. The antifreeze/coolant solution of claim 1, wherein said polymeric polycarboxylate has a molecular weight in a range of between about 500 to 1,800.
5. The antifreeze/coolant solution of claim 1, wherein said azole compound is a mixture of sodium mercaptobenzothiazole and sodium tolytriazole.
6. The antifreeze/coolant solution of claim 5, wherein said sodium mercaptobenzothiazole and sodium tolytriazole are present in a about a 3 to 1 ratio.
7. The antifreeze/coolant solution of claim 1, wherein said azole compound is present in a about a 50% concentration.
8. The antifreeze/coolant solution of claim 1, wherein said nitrate salt is sodium nitrate.
9. The antifreeze/coolant solution of claim 8, wherein said nitrate salt is present in an amount between about 1 wtt to about 3 wtr
10. The antifreeze/coolant solution of claim 1, wherein said phosphate salt is a dipotassium phosphate.
11. The antifreeze/coolant solution of claim 1, wherein said phosphate salt is present in about a 50% solution.
12. The antifreeze/coolant solution of claim 1, wherein said transition metal compound is the disodium salt dihydrate of molybdic acid.
13. The antifreeze/coolant solution of claim 1, including a defoamer.
14. The antifreeze/coolant solution of claim 13, wherein said defoamer is present in an amount between about 0.001 to about 10.0 wt.r
15. The antifreeze/coolant solution of claim 1 , including a bittering agent .
16. The antifreeze/coolant sol ution of cl aim 1 , incl uding a dye.
17. The antifreeze/coolant solution of claim 1 , including a biocide.
18. The antifreeze/coolant solution of claim 1 , wherein said silicone-silicate copolymer is present in an amount between about 0.1 to about 6.0 wt.r
19. The antifreeze/coolant solution of claim 1 , wherein said si l icone-silicate copolymer is selected from the group consi sting of alkali siliconate silylalkylphosphonates and salts thereof, aryl alkyl sil icone sulfonate-silicates and salts thereof, and sulfosiloxane-silicates and salts thereof.
Claim 20. The antifreeze/coolant solution of claim 1, wherein said polymeric polycarboxylate is selected from the group consisting of a secondary alcohol modified polyacrylic acid, a sodium salt of a copolymer of acrylic acid and maleic acid , a polyacryl ic acid or sodium salt thereof having a molecular weight (GPC M of about 2100 and a viscosity (CP at 25°C) ranging from between about 400 to about 1,400, a polyacrylic acid or sodium salt thereof having a molecular weight (GPC M of about 5,100 and a viscosity (CP at 25°C) ranging from between about 250 to about 500, and combinations thereof.
Claim 21. The antifreeze/coolant solution of claim 20, wherein said polyacrylic acid or sodium salt thereof having a molecular weight (GPC M of about 2100 and a viscosity (CP at 25°C) ranging from between about 400 to about 1,400 is GOODRITE® K-752.
Claim 22. The antifreeze/coolant solution of claim 20, wherein said polyacrylic acid or sodium salt thereof having a molecular weight (GPC of about 5,100 and a viscosity (CP at 25°C) ranging from between about 250 to about 500 is GOODRITE® K-732.
Claim 23. An antifreeze/coolant solution for inhibiting the corrosion of metals and inhibiting mineral scale said solution comprising a corrosion inhibiting effective amount of: a polymeric polycarboxylate; a salt which is at least one selected from the group consisting of sodium nitrate, potassium nitrate, magnesium nitrate, calcium nitrate, lithium nitrate and combinations thereof; a salt selected from the group consisting of sodium nitrite, potassium nitrite, magnesium nitrite, calcium nitrite, lithium nitrite and combinations thereof; an azole compound which is selected from the group consisting of sodium mercaptobenzothiazole, sodium tolytriazole, water-soluble triazoles, pyrazoles, imidazoles, isooxazoles, isothiazoles, thiazoles, thiadiazole, 1, 2, 3-benzotriazole, 1,2,3-tolyltriazole, sodium 2-mercaptobenzothiazole, and sodium 2-mercaptobenzimidazole; a silicone-silicate copolymer; a phosphate compound which is selected from the group consisting of dipotassium phosphate, disodium phosphate, monopotassium phosphate, tripotassium phosphate, monosodium phosphate, trisodium phosphate, and mixtures thereof; a transition metal compound selected from the group consisting of disodium salt dihydrate of molybdic acid, molybdenum trioxide, silicoheteropolymolybdates and/or phosphoroheteropolymolybdates, sodium molybdate, potassium molybdate, lithium molybdate, ammonium molybdate, ammonium dimolybdate, and ammonium heptaolybdate; and a glycol compound selected from the group consisting of ethylene glycol, diethylene glycol, propylene glycol, methyl alcohol, ethyl alcohol, propyl alcohol, isopropyl alcohol and combinations thereof making up the balance of the solution.
Claim 24. The antifreeze/coolant solution of claim 23, wherein said polymeric polycarboxylate is selected from the group consisting of a secondary alcohol modified polyacrylic acid, a sodium salt of a copolymer of acrylic acid and maleic acid, a polyacrylic acid or sodium salt thereof having a molecular weight (GPC Mw) of about 2100 and a viscosity (CP at 25°C) ranging from between about 400 to about 1,400, a polyacrylic acid or sodium salt thereof having a molecular weight (GPC M„) of about 5,100 and a viscosity (CP at 25°C) ranging from between about 250 to about 500, and combinations thereof.
Claim 25. The antifreeze/coolant solution of claim 24, wherein said polyacryl ic acid or sodi um salt thereof having a molecular weight (GPC M„) of about 2100 and a viscosity (CP at 25°C) ranging from between about 400 to about 1,400 is GOODRITE® K-752.
Claim 26. The antifreeze/cool ant sol ution of cl aim 24, wherein said polyacrylic acid or sodium salt thereof having a molecular weight (GPC
Figure imgf000036_0001
of about 5, 100 and a vi scosity (CP at 25°C) ranging from between about 250 to about 500 i s GOODRITE® K-732
Claim 27. The antifreeze/coolant solution of claim 23, wherein said polymeric polycarboxylate comprises from about 0.001 to about 10 0 percent by weight.
Claim 28. The antifreeze/coolant sol ution of claim 23, wherein said nitrate salt compri ses an amount of about 0.1 to about 10 0 percent by weight.
Claim 29. The antifreeze/cool ant sol ution of claim 23, wherein said nitrate salt comprises an amount of about 0.01 to about 1.0 percent by weight
Claim 30. The antifreeze/coolant sol ution of claim 23, wherein said nitrite salt comprises an amount of about 0.01 to about 10.0 percent by weight.
Claim 31. The antifreeze/coolant sol ution of claim 23, wherein said nitrite salt comprises an amount of about 0.1 to about
1.0 percent by weight.
Claim 32. The antifreeze/coolant solution of claim 23, wherein said azole compound comprises an amount of about 0.01 to about 1.0 percent by weight.
Claim 33. The antifreeze/coolant solution of claim 23, wherein said silicone-silicate copolymer comprises an amount of about 0.1 to about 10.0 percent by weight.
Claim 34. The antifreeze/coolant solution of claim 23, wherein said phosphate salt comprises an amount providing a concentration of about 0.5 to about 2 parts by weight per 100 parts by weight.
Claim 35. The antifreeze/coolant solution of claim 23, wherein said transition metal compound an amount of from about 0.001 to about 10.0 percent by weight.
PCT/US1999/011324 1998-05-22 1999-05-21 Diesel engine antifreeze composition WO1999061545A1 (en)

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AU40943/99A AU743301B2 (en) 1998-05-22 1999-05-21 Diesel engine antifreeze composition
CA002333046A CA2333046C (en) 1998-05-22 1999-05-21 Diesel engine antifreeze composition
AT00913616T ATE493481T1 (en) 1999-02-26 2000-02-25 ANTIFREEZE FOR DIESEL ENGINES BASED ON MONOCARBOXYLIC ACIDS
CA002363660A CA2363660C (en) 1999-02-26 2000-02-25 Monocarboxylic acid based antifreeze composition for diesel engines
BRPI0010276-8B1A BR0010276B1 (en) 1999-02-26 2000-02-25 antifreeze composition based on monocarboxylic acid
AU35029/00A AU772428B2 (en) 1999-02-26 2000-02-25 Monocarboxylic acid based antifreeze composition for diesel engines
CNB008059918A CN1200990C (en) 1999-02-26 2000-02-25 Monocarboxylic acid based antifreeze composition for diesel engines
EP00913616A EP1159372B1 (en) 1999-02-26 2000-02-25 Monocarboxylic acid based antifreeze composition for diesel engines
MXPA01008616A MXPA01008616A (en) 1999-02-26 2000-02-25 Monocarboxylic acid based antifreeze composition for diesel engines.
DE60045442T DE60045442D1 (en) 1999-02-26 2000-02-25 ANTIFREEZE FOR DIESEL ENGINES BASED ON MONOCARBONIC ACIDS
PCT/US2000/004850 WO2000050532A1 (en) 1999-02-26 2000-02-25 Monocarboxylic acid based antifreeze composition for diesel engines
DK00913616.9T DK1159372T3 (en) 1999-02-26 2000-02-25 Monocarboxylic acid-based coolant composition for diesel engines

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CN103694966B (en) * 2013-09-30 2016-08-24 安阳化学工业集团有限责任公司 Process units and the technique thereof of engine coolant is prepared with coal-ethylene glycol waste material
CN103666389B (en) * 2013-09-30 2016-08-24 安阳化学工业集团有限责任公司 The engine coolant prepared with coal-ethylene glycol waste material
CN104893687A (en) * 2015-06-03 2015-09-09 辽宁石油化工大学 Method for directly preparing anti-freezing solution by quickly treating coal-to-ethylene glycol technology waste liquid by inorganic base
CN104893687B (en) * 2015-06-03 2018-05-29 辽宁石油化工大学 A kind of method that coal-ethylene glycol process waste liquor anti-icing fluid directly processed is quickly handled using inorganic base
US10307344B2 (en) * 2016-02-15 2019-06-04 Shofu Inc. Two-paste type sealer composition for root canal filling
CN113930221A (en) * 2021-10-27 2022-01-14 常州市鑫光化工科技有限公司 Special cooling liquid for diesel locomotive
CN113930221B (en) * 2021-10-27 2023-12-26 常州市鑫光新材料科技有限公司 Special coolant for diesel locomotive
CN114672287A (en) * 2022-04-01 2022-06-28 陶普斯化学科技(北京)有限公司 High-corrosion-inhibition low-conductivity heat transfer medium and preparation method and application thereof
CN114672287B (en) * 2022-04-01 2023-08-18 陶普斯化学科技(北京)有限公司 High corrosion inhibition low conductivity heat transfer medium and preparation method and application thereof
CN116463632A (en) * 2023-04-28 2023-07-21 营口星火新材料有限公司 Corrosion inhibition complexing agent for hydrogen fuel cell cooling liquid and preparation method and application thereof

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AU743301B2 (en) 2002-01-24
CN1246415C (en) 2006-03-22
AU4094399A (en) 1999-12-13
CA2333046A1 (en) 1999-12-02
CA2333046C (en) 2007-02-06
CN1308663A (en) 2001-08-15

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