US20040072702A1 - Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax - Google Patents

Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax Download PDF

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Publication number
US20040072702A1
US20040072702A1 US10/467,151 US46715103A US2004072702A1 US 20040072702 A1 US20040072702 A1 US 20040072702A1 US 46715103 A US46715103 A US 46715103A US 2004072702 A1 US2004072702 A1 US 2004072702A1
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radicals
carbon atoms
lubricant
mixture
phosphate ester
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Dominique Raison
Jean-Guy Le Helloco
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Rhodia Chimie SAS
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Rhodia Chimie SAS
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Assigned to CHIMIE, RHODIA reassignment CHIMIE, RHODIA ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LE HELLOCO, JEAN-GUY, RAISON, DOMINIQUE
Publication of US20040072702A1 publication Critical patent/US20040072702A1/en
Priority to US11/866,850 priority Critical patent/US7776799B2/en
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/06Particles of special shape or size
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty oils
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/08Inorganic acids or salts thereof
    • C10M2201/084Inorganic acids or salts thereof containing sulfur, selenium or tellurium
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/18Ammonia
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/18Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/127Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids polycarboxylic
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
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    • C10N2010/04Groups 2 or 12
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    • C10N2010/12Groups 6 or 16
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    • C10N2010/14Group 7
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    • C10N2010/16Groups 8, 9, or 10
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    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/055Particles related characteristics
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/243Cold working
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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    • C10N2040/244Metal working of specific metals
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/245Soft metals, e.g. aluminum
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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    • C10N2040/244Metal working of specific metals
    • C10N2040/246Iron or steel
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    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/247Stainless steel

Definitions

  • the subject of the present invention is a cold rolling process for metals using an aqueous lubricant comprising a mixture based on at least one carboxylic acid, on at least one phosphate ester and including at least one wax.
  • lubricants such as for example whole oils and aqueous lubricants.
  • the other additives used are based on sulfur (sulfur-containing esters, sulfur-containing oils) or based on phosphorus (phosphate esters) or mixtures thereof. They result in the formation of a metal sulfide or a metal phosphate.
  • the object of the present invention is to propose a cold rolling process for metals that does not have the drawbacks of the usual processes.
  • the process according to the invention makes it possible to work under very severe conditions, representative of high-productivity conditions, while still maintaining the surface finish (coloration, brightness) of the deformed metal.
  • a cold rolling process for metals using an aqueous lubricant comprising (1) at least one mixture based on at least one acid chosen from saturated or unsaturated, monocarboxylic or polycarboxylic acids containing 5 to 40 carbon atoms; on at least one acid phosphate ester of formula (RO) x —P( ⁇ O) (OH) x′ , in which formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3; the carboxylic acid and/or the acid phosphate ester being optionally neutralized by an organic or mineral base; and (2) at least one natural or synthetic wax having a melting point not less than 50° C. and having a mean particle size ranging between 0.5-10 ⁇ m.
  • formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3
  • the size measurements are carried out either by laser diffraction or by light scattering. There is no difficulty for those skilled in the art to choose one of these two methods depending on the size of the objects.
  • conventional lubricant is understood to mean either a whole oil containing one or more extreme-pressure additives, or an aqueous lubricant also containing one or more extreme-pressure additives. It should be noted that conventional extreme-pressure additives are compounds containing phosphorus (such as for example phosphates) or sulfur (such as especially sulfonates).
  • an aqueous lubricant according to the invention allows the productivity of cold rolling operations to be significantly improved.
  • this lubricant it is possible to increase the thickness reduction ratio of the rolled metal by at least 15%, more particularly by at least 20% and highly advantageously by at least 30%, compared with the maximum reduction ratio achievable by a rolling mill using a conventional lubricant, whether a whole oil containing one or more extreme-pressure additives or an aqueous lubricant containing one or more extreme-pressure additives.
  • the aqueous lubricant comprises at least one mixture based on at least one acid chosen from saturated or unsaturated, monocarboxylic or polycarboxylic acids containing 5 to 40 carbon atoms; on at least one acid phosphate ester of formula (RO) x —P( ⁇ O) (OH) x′ , in which formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3, the carboxylic acid and/or the acid phosphate ester being optionally neutralized by an organic or mineral base.
  • formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3, the carboxylic acid and/or the acid phosphate ester being optionally neutralized by an organic or mineral base.
  • the mixture (1) may be an aqueous solution or an aqueous dispersion.
  • the term “dispersion” denotes a dispersion of vesicles, droplets or micelles in an aqueous medium.
  • the carboxylic acid used possesses one or more carboxylic functional groups and at least one radical containing 5 to 40 carbon atoms, said radical being a linear or branched, alkyl or alkenyl radical having one or more ethylenically unsaturated groups (carbon-carbon double bonds) and optionally being substituted with one or more hydroxyl radicals.
  • the acid possesses one or more carboxylic functional groups and a radical containing 7 to 30 carbon atoms, optionally substituted with one or more hydroxyl radicals and optionally having one or more ethylenically unsaturated groups.
  • said acid possesses one carboxylic functional group or two.
  • this second functional group may or may not be at the end of the chain.
  • the carboxylic acid is a saturated or unsaturated fatty acid, more particularly comprising a single carboxylic functional group, or a mixture of several fatty acids.
  • saturated fatty acids mention may be made of caproic, caprylic, capric, lauric, myristic, stearic, isostearic, palmitic, behenic and lignoceric acids.
  • unsaturated fatty acids examples include the unsaturated fatty acids having a single ethylenically unsaturated group, such as linderic, myristoleic, palmitoleic, oleic and erucic acids; unsaturated fatty acids having two ethylenically unsaturated groups, such as linoleic acid; unsaturated fatty acids having three ethylenically unsaturated groups, such as linolenic acid; and unsaturated fatty acids carrying a hydroxyl group, such as ricinoleic acid, as well as mixtures thereof.
  • unsaturated fatty acids having a single ethylenically unsaturated group such as linderic, myristoleic, palmitoleic, oleic and erucic acids
  • unsaturated fatty acids having two ethylenically unsaturated groups such as linoleic acid
  • R is a hydrocarbon radical containing 1 to 30 carbon atoms, said radical being a saturated or unsaturated, aliphatic or cycloaliphatic radical or an aromatic radical.
  • the radicals R which are identical or different, are linear or branched radicals containing 8 to 26 carbon atoms, these being alkyl radicals or alkenyl radicals carrying one or more ethylenically unsaturated groups.
  • radicals R which may or may not be identical, may be aromatic radicals carrying alkyl, arylalkyl or alkylaryl substituents, these radicals containing 6 to 30 carbon atoms.
  • aromatic radicals carrying alkyl, arylalkyl or alkylaryl substituents, these radicals containing 6 to 30 carbon atoms.
  • the OA groups which may or may not be identical, correspond to an oxyethylene, oxypropylene or oxybutylene radical, or mixtures thereof.
  • said group corresponds to an oxyethylene and/or oxypropylene radical.
  • this is preferably between 0 and 80.
  • the acid phosphate ester forming part of the composition of the mixture (1) may be formed from a combination of several of them.
  • carboxylic acid and/or the acid phosphate ester may be in a form neutralized by a mineral or organic base.
  • bases used are preferably water-soluble.
  • water-soluble bases is understood to mean compounds soluble in an aqueous medium, at 20° C., with a concentration of from 3 to 7% by weight.
  • the bases employed are organic bases but are more particularly chosen from primary, secondary or tertiary amines or polyamines comprising at least one linear, branched or cyclic hydrocarbon radical having 1 to 40 carbon atoms, said radical being optionally substituted with one or more hydroxyl radicals and/or one or more alkoxylated groups.
  • the said alkoxylated groups are preferably ethoxylated units.
  • the number of alkoxylated units, if present, is less than or equal to 100.
  • the amines when the amines have at least two amine functional groups, said functional groups are separated in pairs by a number of carbon atoms ranging between 2 and 5.
  • Suitable amines mention may be made of monoethanolamine, diethanolamine, ethylenediamine, aminoethylethanolamine and aminomethylpropanolamine.
  • Polyalkoxylated fatty amines may also be used as organic base, such as for example those sold by Rhodia Chimie under the name RHODAMEEN® CS20.
  • At least the carboxylic acid is neutralized by an organic base, the amount of the latter being such that the total number of moles of amine functional groups is at least equal to the total number of moles of carboxylic acid functional groups, and preferably at least twice as large.
  • the mixture (1) may optionally furthermore include at least one nonionic surfactant.
  • the use of this type of compound may be desired when the mixture (1) is in the form of a dispersion.
  • polyalkoxylated alkylphenols in particular those in which the alkyl substituent is a C 6 -C 12 one;
  • polyalkoxylated mono-, di- or tri-(alkylaryl)phenol preferably chosen from those in which the alkyl substituent is a C 1 -C 6 one;
  • polyalkoxylated aliphatics more particularly C 8 -C 22 alcohols
  • polyalkoxylated units if present, of these nonionic surfactants usually varies from 2 to 100. It should be noted that the term “polyalkoxylated units” is understood to mean ethoxylated units, propoxylated units or mixtures thereof.
  • the amount of surfactant usually varies, if it is present, between 1 and 30% by total weight of the mixture (1).
  • the contents of carboxylic acid, of acid phosphate ester, optionally of base, preferably an organic base, and optionally of nonionic surfactant are such that the solids content of the aqueous medium is at least 10% by weight. More precisely, the solids content is between 10 and 70% by weight. Preferably, the solids content varies between 10 and 40% by weight.
  • the pH of the mixture (1) ranges between 7 and 9. This pH range may inter alia be achieved by the addition of a buffer agent to said mixture.
  • said mixture (1) is combined with at least one metal in the form of a multivalent ion. More particularly, said metal may be in the form of a divalent ion or a trivalent ion. Likewise, it would not be excluded to use several metals, in identical or different oxidation states.
  • said metal is chosen from columns IIA, VIII, IB, IIB and VIB, with the exception of cobalt and nickel.
  • the metals are chosen from calcium, magnesium, copper, zinc, iron, aluminum and chromium, by themselves or as mixtures.
  • the mixture (1) associated with the metal is more precisely in the form of a dispersion comprising lamellar crystallites having a length ranging between 0.1 and 100 ⁇ m, a width ranging between 0.5 and 30 ⁇ m and a thickness ranging between 5 and 200 nm.
  • These crystallites comprise a stack of organic phases (O) and of aqueous solutions (A) in the sequence O/[A/O]n, n being an integer different from 0 and such that a stack has a thickness of 5 to 200 nm. More particularly, n is between 1 and 20.
  • the size of the crystallites their length is advantageously between 0.5 and 20 ⁇ m.
  • the width of the lamellar crystallites is more particularly between 0.5 and 10 ⁇ m.
  • the thickness of the lamellar crystallites is preferably between 10 and 100 nm.
  • the abovementioned dimensions of the lamellar crystallites correspond to average values. In other words, there is a distribution in the sizes of the lamellar crystallites, the average of which lies within the above ranges.
  • the measurements of the dimensions of the lamellar crystallites are carried out using transmission electron microscopy on a specimen vitrified cryogenically (Cryo-Met—see O. Aguerre-Chariol, M. Deruelle, T.
  • the crystallites are advantageously used in the presence of at least one nonionic surfactant.
  • the crystallites may be obtained by bringing a solution or dispersion containing the acid phosphate ester and the optionally neutralized carboxylic acid into contact with the metal in ionic and/or metallic form.
  • this may equally well be in its metallic form or in the form of a multivalent cation.
  • Said cation may itself be in the form of a solid, a solution or a dispersion.
  • the metal is used in the form of a solution, preferably an aqueous solution
  • a solution preferably an aqueous solution
  • salts of mineral acids such as halides, with chlorides for example, or nitrates
  • salts or organic acids such as, among others, formates and acetates.
  • metal in an oxide, hydroxide or carbonate form, or the metal itself.
  • the contacting is carried out in the presence of at least one compound having the effect of buffering the pH. More particularly, one or more compounds are chosen such that the pH of the medium is between 7 and 9.
  • the contacting takes place with stirring.
  • the metal in the chosen form is introduced into the mixture (1), the carboxylic acid preferably being neutralized by an organic base.
  • the operation advantageously takes place at a temperature below 100° C. and preferably at a temperature ranging between 20 and 60° C.
  • the aqueous lubricant used in the cold rolling process according to the invention furthermore includes at least one natural or synthetic wax, having a melting point not less than 50° C. and having a mean particle size ranging between 0.5-10 ⁇ m.
  • the wax or waxes are dispersed within the mixture (1) in a homogeneous and stable manner.
  • these waxes are chosen from natural waxes of the type consisting of paraffin waxes or synthetic waxes having ester and/or amide functional groups.
  • the waxes used are those having amide functional groups.
  • Said waxes may be obtained, for example, by a condensation reaction, and more particularly by a reaction of an ester or acid functional group with an amine functional group.
  • these waxes have a degree of polymerization of at most 10 and advantageously at most 3.
  • the aforementioned waxes correspond to the following formula: R′—CO-A-(CR′′ 2 ) n′′ A-CO′R′, in which formula the radicals R′, which may or may not be identical, represent an aliphatic radical containing 5 to 22 carbon atoms, said radical being saturated or having one or more conjugated or nonconjugated carbon-carbon double bonds; the radicals R′′, which may or may not be identical, represent a hydrogen atom or an alkyl radical containing 1 to 4 carbon atoms; n represents an integer between 2 and 12; and the radicals A, which may or may not be identical, represent —O— or —NH—. It should be noted that the radicals A are preferably of the same type.
  • the melting point of the waxes is not less than 80° C.
  • the wax content in the aqueous lubricant during its use is between 0.05 and 10% by weight of the lubricant, preferably between 0.05 and 5% by weight of the lubricant.
  • the wax may be introduced into the mixture either by incorporating the wax particles, the size of which lies within the abovementioned range, into said mixture. It is also possible to introduce the wax by adding the latter in molten form to the mixture, and to precipitate it in the mixture, the operation advantageously taking place by carrying out a grinding operation so as to obtain the appropriate size of particles.
  • the aqueous lubricants according to the invention may also include additives that are conventional in this field, such as preservatives, anticorrosion agents, antifoams and stabilizers.
  • the metals on which such treatments may be carried out are especially, and mainly, steels, stainless steels, aluminum, copper, zinc, tin, copper-based alloys (bronze, brass), etc.
  • the present invention is most particularly applicable to the cold rolling of stainless steel.
  • the rolled metal was coiled stainless steel, 10 mm in width and about 0.4 mm in thickness.
  • the applied force on the rolls varied from 200 metric tonnes/m to 1200 metric tonnes/m, so as to obtain a sheet reduction ratio varying from 20 to 55%.
  • the lubricant according to the invention made it possible to obtain, for a linear speed of the rolls of 5 m/s, reduction ratios of at least 55% without having reached the clamping limit of the rolling mill.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
US10/467,151 2001-02-05 2002-02-05 Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax Abandoned US20040072702A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/866,850 US7776799B2 (en) 2001-02-05 2007-10-03 Cold rolling process for metals using an aqueous lubricant comprising at least one carboxylic acid, one phosphate ester and one wax

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR01/01566 2001-02-05
FR0101566A FR2820431B1 (fr) 2001-02-06 2001-02-06 Procede de deformation de metaux mettant en oeuvre un lubrifiant aqueux additive permettant d'augmenter la productivite
PCT/FR2002/000436 WO2002062931A1 (fr) 2001-02-05 2002-02-05 Procede de laminage a froid de metaux utilisant un lubrifiant aqueux comprenant au moins un acide carboxylique, un ester phosphate et une cire

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US10/467,151 Abandoned US20040072702A1 (en) 2001-02-05 2002-02-05 Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax
US11/866,850 Expired - Fee Related US7776799B2 (en) 2001-02-05 2007-10-03 Cold rolling process for metals using an aqueous lubricant comprising at least one carboxylic acid, one phosphate ester and one wax

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US (2) US20040072702A1 (fr)
EP (1) EP1358305A1 (fr)
JP (1) JP4017523B2 (fr)
KR (1) KR100512088B1 (fr)
CN (1) CN1272416C (fr)
AU (1) AU2002235983B2 (fr)
BR (1) BR0206983A (fr)
CA (1) CA2437601C (fr)
FR (1) FR2820431B1 (fr)
MX (1) MXPA03006878A (fr)
RU (1) RU2265645C2 (fr)
WO (1) WO2002062931A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2913355A1 (fr) * 2007-03-08 2008-09-12 Michelin Soc Tech Procece de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques
FR2913356A1 (fr) * 2007-03-08 2008-09-12 Rhodia Recherches & Tech Lubrification par des dispersions dans des procedes de deformation des metaux

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010129953A1 (fr) * 2009-05-08 2010-11-11 Quaker Chemical Corporation Lubrifiant à solution aqueuse pour laminage à froid de l'acier
CA2835019C (fr) * 2011-05-06 2018-04-10 Chemetall Gmbh Fluide de travail de metal sans cov sans amine
JP5890152B2 (ja) * 2011-11-17 2016-03-22 出光興産株式会社 水溶性金属加工油剤、金属加工液、及び金属加工方法
KR102075213B1 (ko) * 2017-12-21 2020-02-07 주식회사 포스코 열연강판 냉각용 조성물 및 이를 이용한 열연 강판의 냉각 방법
EP4006184A4 (fr) 2019-07-31 2022-08-31 JFE Steel Corporation Tôle d'acier électromagnétique non orienté et procédé pour sa fabrication
CN113462448A (zh) * 2021-06-08 2021-10-01 青岛华瑞泰格工贸有限公司 一种可生物降解的低发烟型金属挤压攻丝油

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3928401A (en) * 1974-01-31 1975-12-23 Emery Industries Inc Water soluble triglyceride compositions and method for their preparation
US3966619A (en) * 1974-11-04 1976-06-29 Alcan Research And Development Limited Lubricants for cold working of aluminium
US4462920A (en) * 1983-06-06 1984-07-31 The Dow Chemical Company Water-based hydraulic fluids
US4481038A (en) * 1983-06-29 1984-11-06 Glyco Inc. Water dispersible fatty acid bis-amides
US4612127A (en) * 1983-09-28 1986-09-16 Hitachi, Ltd. Lubricant for metal forming and process for metal forming
US5076339A (en) * 1990-02-08 1991-12-31 Smith John J Solid lubricant for die casting process
US6806238B1 (en) * 1999-10-21 2004-10-19 Rhodia Chimie Use of lamellar crystallites as extreme pressure additives in aqueous lubricants, lamellar crystallites and method for obtaining same

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB358202A (en) * 1930-08-14 1931-10-08 Chem Ind Basel Manufacture of disperse systems
GB361860A (en) * 1930-08-19 1931-11-19 Wilfred William Groves Manufacture of disperse systems
NL80211C (fr) * 1950-05-24
US3522177A (en) * 1967-12-26 1970-07-28 Standard Pressed Steel Co Aqueous lubricant composition
US3637498A (en) * 1968-04-29 1972-01-25 Aluminum Co Of America Extrusion lubricant
US3551335A (en) * 1969-02-14 1970-12-29 Pennwalt Corp Metal working lubricants
DE2046727B2 (de) * 1970-09-22 1973-04-19 Dow Corning GmbH, 8000 München Hochtemperaturschmiermittel fuer die spanlose metallumformung
FR2130981A5 (fr) * 1971-03-29 1972-11-10 Rhone Poulenc Sa
US4362634A (en) * 1980-03-19 1982-12-07 Stauffer Chemical Company Metal working lubricant and lubricant emulsion
US4474669A (en) * 1980-06-02 1984-10-02 United States Steel Corporation Can-making lubricant
JPS59227986A (ja) * 1983-06-10 1984-12-21 Kao Corp 金属加工油組成物
JPS62192496A (ja) * 1986-02-19 1987-08-24 Kao Corp アルミ用冷間圧延油組成物
US4743388A (en) * 1986-07-21 1988-05-10 Westvaco Corporation Complex amide carboxylate lubricant rust inhibitor additive for metal working fluids
US4758359A (en) * 1987-03-16 1988-07-19 Reynolds Metals Company Aqueous metal working lubricant containing a complex phosphate ester
JPH07112564B2 (ja) * 1987-09-28 1995-12-06 日新製鋼株式会社 ステンレス鋼の熱間圧延用潤滑剤
US5211861A (en) * 1988-09-19 1993-05-18 Ausimont S.R.L. Liquid aqueous compositions comprising perfluoropolyethereal compounds suitable as lubricants in the plastic processing of metals
GB8926885D0 (en) * 1989-11-28 1990-01-17 Albright & Wilson Drilling fluids
TW296990B (fr) * 1994-03-25 1997-02-01 Nissin Seiko Kk
PY970104A (es) * 1996-08-30 2001-12-03 Monsanto Co Nuevos fluidos solubles en agua para trabajar metales
FR2758561B1 (fr) * 1996-11-25 1999-04-23 Rhodia Chimie Sa Compositions d'orthophosphates soufres, leur procede de preparation et leur utilisation
US5837658A (en) * 1997-03-26 1998-11-17 Stork; David J. Metal forming lubricant with differential solid lubricants
DE19852203A1 (de) * 1998-11-12 2000-05-18 Henkel Kgaa Schmiermittel mit Feststoffpartikeln einer Teilchengröße unter 500 nm
EP1123965A1 (fr) * 2000-02-08 2001-08-16 Mobil Oil Francaise Composition d'huile pour le laminage à froid d'acier et d'acier inoxydable

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3928401A (en) * 1974-01-31 1975-12-23 Emery Industries Inc Water soluble triglyceride compositions and method for their preparation
US3966619A (en) * 1974-11-04 1976-06-29 Alcan Research And Development Limited Lubricants for cold working of aluminium
US4462920A (en) * 1983-06-06 1984-07-31 The Dow Chemical Company Water-based hydraulic fluids
US4481038A (en) * 1983-06-29 1984-11-06 Glyco Inc. Water dispersible fatty acid bis-amides
US4612127A (en) * 1983-09-28 1986-09-16 Hitachi, Ltd. Lubricant for metal forming and process for metal forming
US5076339A (en) * 1990-02-08 1991-12-31 Smith John J Solid lubricant for die casting process
US5076339B1 (en) * 1990-02-08 1998-06-09 J & S Chemical Corp Solid lubricant for die-casting process
US6806238B1 (en) * 1999-10-21 2004-10-19 Rhodia Chimie Use of lamellar crystallites as extreme pressure additives in aqueous lubricants, lamellar crystallites and method for obtaining same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2913355A1 (fr) * 2007-03-08 2008-09-12 Michelin Soc Tech Procece de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques
FR2913356A1 (fr) * 2007-03-08 2008-09-12 Rhodia Recherches & Tech Lubrification par des dispersions dans des procedes de deformation des metaux
WO2008110493A1 (fr) * 2007-03-08 2008-09-18 Rhodia Operations Lubrification par des dispersions dans des procédés de déformation des métaux
WO2008113481A1 (fr) * 2007-03-08 2008-09-25 Societe De Technologie Michelin Procede de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques
US20100170624A1 (en) * 2007-03-08 2010-07-08 Societe De Technologie Michelin Method for the Wet Drawing of Steel Cables for Reinforcing Tires
US8555689B2 (en) * 2007-03-08 2013-10-15 Michelin Recherche Et Technique S.A. Method for the wet drawing of steel cables for reinforcing tires

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KR20030082584A (ko) 2003-10-22
KR100512088B1 (ko) 2005-09-02
RU2003127020A (ru) 2005-02-27
US7776799B2 (en) 2010-08-17
CA2437601A1 (fr) 2002-08-15
AU2002235983B9 (en) 2002-08-19
FR2820431A1 (fr) 2002-08-09
FR2820431B1 (fr) 2007-04-27
EP1358305A1 (fr) 2003-11-05
CN1494584A (zh) 2004-05-05
US20080028812A1 (en) 2008-02-07
AU2002235983B2 (en) 2004-10-14
RU2265645C2 (ru) 2005-12-10
CA2437601C (fr) 2011-01-11
CN1272416C (zh) 2006-08-30
BR0206983A (pt) 2004-02-10
JP4017523B2 (ja) 2007-12-05
MXPA03006878A (es) 2005-04-11
WO2002062931A1 (fr) 2002-08-15
JP2004527598A (ja) 2004-09-09

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