EP1230331B1 - Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention - Google Patents
Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention Download PDFInfo
- Publication number
- EP1230331B1 EP1230331B1 EP00971481A EP00971481A EP1230331B1 EP 1230331 B1 EP1230331 B1 EP 1230331B1 EP 00971481 A EP00971481 A EP 00971481A EP 00971481 A EP00971481 A EP 00971481A EP 1230331 B1 EP1230331 B1 EP 1230331B1
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- EP
- European Patent Office
- Prior art keywords
- lamellar crystallites
- range
- carbon atoms
- lamellar
- use according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000314 lubricant Substances 0.000 title claims abstract description 23
- 239000005069 Extreme pressure additive Substances 0.000 title claims abstract description 7
- 238000000034 method Methods 0.000 title claims abstract description 5
- 229910052751 metal Inorganic materials 0.000 claims abstract description 40
- 239000002184 metal Substances 0.000 claims abstract description 40
- 239000002253 acid Substances 0.000 claims abstract description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 26
- 239000012074 organic phase Substances 0.000 claims abstract description 22
- 150000002739 metals Chemical class 0.000 claims abstract description 12
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 10
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 10
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 9
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 8
- 239000011707 mineral Substances 0.000 claims abstract description 8
- 239000007864 aqueous solution Substances 0.000 claims abstract description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract 8
- 230000001131 transforming effect Effects 0.000 claims abstract 2
- -1 phosphate ester Chemical class 0.000 claims description 18
- 150000007513 acids Chemical class 0.000 claims description 15
- 239000006185 dispersion Substances 0.000 claims description 14
- 229910019142 PO4 Inorganic materials 0.000 claims description 10
- 239000010452 phosphate Substances 0.000 claims description 10
- 239000002585 base Substances 0.000 claims description 9
- 150000002500 ions Chemical class 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- 150000007530 organic bases Chemical class 0.000 claims description 5
- 229910001369 Brass Inorganic materials 0.000 claims description 4
- 229910000831 Steel Inorganic materials 0.000 claims description 4
- 239000010951 brass Substances 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 239000010959 steel Substances 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 239000012736 aqueous medium Substances 0.000 claims description 3
- 150000007514 bases Chemical class 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 238000011282 treatment Methods 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 2
- 229910000906 Bronze Inorganic materials 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 239000010974 bronze Substances 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000003141 primary amines Chemical group 0.000 claims description 2
- 229910001220 stainless steel Inorganic materials 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 239000011135 tin Substances 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 239000004411 aluminium Substances 0.000 claims 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 claims 1
- 150000003014 phosphoric acid esters Chemical class 0.000 abstract description 2
- 229920001281 polyalkylene Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 11
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 150000001735 carboxylic acids Chemical class 0.000 description 5
- 230000009466 transformation Effects 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 3
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000004627 transmission electron microscopy Methods 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- MUBKMWFYVHYZAI-UHFFFAOYSA-N [Al].[Cu].[Zn] Chemical compound [Al].[Cu].[Zn] MUBKMWFYVHYZAI-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 125000005645 linoleyl group Chemical group 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating 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
- C10M171/06—Particles of special shape or size
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/055—Particles related characteristics
- C10N2020/06—Particles of special shape or size
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
Definitions
- the present invention relates to the use, as extreme pressure additives in aqueous lubricants, lamellar crystallites. It also concerns these lamellar crystallites and their production.
- the subject of the present invention is the use in aqueous lubricants, as as extreme pressure additives of lamellar crystallites, of micron size, and comprising a stack of organic phases and aqueous solutions; said crystallites being dispersed within the aqueous lubricant.
- these lamellar crystallites whose length is less than or equal to 100 ⁇ m, the width less than or equal to 30 ⁇ m and the thickness less than or equal to 200 nm, come into contact with the surface of the metal to be transformed, and that they favor the lubrication, by a slip of the lamellar crystallites the in relation to each other, during the transformation / deformation operation.
- the attached figure represents a photograph taken by transmission electron microscopy (Cryo-MET, full scale of photography: 2 ⁇ m). It represents lamellar crystallites according to the invention.
- a second subject of the invention consists of such lamellar crystallites.
- Another object of the invention consists in obtaining crystallites lamellar.
- the method comprises contacting a solution or a dispersion comprising the optionally neutralized acid, with the metal occurring under a ionic and / or metallic form.
- said lamellar crystallites present a length of between 0.1 and 100 ⁇ m.
- the length of the crystallites lamellar is between 0.5 and 20 ⁇ m.
- the lamellar crystallites moreover have a width varying between 0.5 and 30 .mu.m. More particularly, the width of the lamellar crystallites is between 0.5 and 10 ⁇ m.
- the thickness of the lamellar crystallites is between 5 and 200 nm, preferably between 10 and 100 nm.
- the dimensions of the lamellar crystallites which have just been indicated correspond to average values. In other words, there is a distribution of sizes of lamellar crystallites whose average is in the ranges above.
- the lamellar crystallites are more particularly constituted of a stack organic phases (O) and aqueous solutions (A) according to the sequence O / [A / O] n, n being an integer different from 0 and such that the stack has a thickness from 5 to 200 nm.
- n is a positive integer that can be at most 100. preferably, n is an integer between 1 and 20.
- said acids are optionally in a form neutralized by a organic or mineral base.
- the carboxylic acids likely to enter the composition of the organic phases of the lamellar crystallites according to the invention are selected from saturated or unsaturated mono- or polycarboxylic acids comprising from 5 to 40 carbon atoms.
- R 1 - COOH corresponds to the following formula: R 1 - COOH; formula in which R 1 represents an alkyl, alkenyl radical having one or more ethylenic unsaturations, linear or branched, having from 5 to 40 carbon atoms (the carbon atom of the carboxylic group being included), optionally substituted by one or more radicals; hydroxyls and / or at least one carboxylic function.
- the acid corresponds to the above formula, in which R 1 represents an alkyl radical comprising 7 to 30 carbon atoms, optionally substituted by one or more hydroxyl radicals and / or one or more preferably a carboxylic function.
- the second carboxylic function if present, can be find end of chain or not.
- the organic phase i) is derived from at least one fatty acid, comprising more particularly a single carboxylic function.
- saturated fatty acids mention may be made of stearic acids, palmitic, behenic.
- unsaturated fatty acids include unsaturated fatty acids having a single double bond such as linderic, myristoleic, palmitoleic, oleic, petroselenic, doeglic, gadoleic, erucic; fatty acids unsaturated having two double bonds such as linoleic acid; fatty acids unsaturated having 3 double bonds such as linolenic acid; fatty acids unsaturated having more than 4 double bonds such as isanic acids, stearodonic, arachidonic, cypranodonic; unsaturated fatty acids carrying hydroxyl group such as ricinoleic acid and mixtures thereof.
- the acids are preferably used. palmitic, behenic, stearic, palmitoleic, oleic, petroselenic, erucic, linoleic, linolenic, ricinoleic.
- (RO) x -P ( O) (OH) x ' formula, in which R, identical or not, represent a hydrocarbon radical, optionally polyalkoxylated, x and x 'being equal to 1 or 2, provided that the sum of x and x' is equal to 3.
- R is an aliphatic, cycloaliphatic hydrocarbon radical or aromatic, saturated or unsaturated, containing 1 to 30 carbon atoms.
- the radicals R which are identical or different, are alkyl or alkenyl radicals carrying one or more linear or branched ethylenic unsaturations containing 8 to 26 carbon atoms.
- the radicals R may be aromatic radicals bearing alkyl, arylalkyl substituents, or alkylaryl; these radicals comprising 6 to 30 carbon atoms.
- such radicals include, inter alia, nonylphenyl, mono-, di- and tristyrylphenyl radicals.
- the OA group corresponds to an oxyethylenated radical, oxypropylene, oxybutylenated, or mixtures thereof.
- said grouping corresponds to an oxyethylenated and / or oxypropylenated radical.
- y average, it is preferably between 0 and 80.
- the acid used in the composition of organic phases of the lamellar crystallites may be in a form neutralized by a mineral or organic base.
- the bases that can be used to neutralize the acid, the basic compounds which create monovalent species are suitable.
- bases used are preferably water-soluble.
- alkali metal hydroxides hydroxycarbonates, carbonates, bicarbonates, ammonia.
- Suitable organic bases include, but are not limited to, primary, secondary or tertiary amines comprising 1 to 40 carbon atoms, optionally substituted with one or more hydroxyl radicals, and / or one or several oxyalkylenated groups.
- Said alkylenated groups are preferably oxyethylenated units.
- the number of oxyalkylenated units, are present is less than or equal to 100.
- Suitable amines mention may be made of monoethanolamine, diethanolamine, ethylenediamine, aminoethylethanolamine, aminomethylpropanolamine.
- Polyoxyalkylenated fatty amines can also be used in as an organic basis, such as those marketed by Rhodia Chemistry under the name Rhodameene® CS20.
- the lamellar crystallites further comprise at least one metal in the form of a multivalent ion. More particularly, said metal can be in the form of a divalent ion or a trivalent ion. It is likewise not excluded to implement several metals, with identical or different degrees of oxidation.
- said metal is chosen from columns IIA, VIII, IB, IIB, with the exception of cobalt and nickel.
- the metals are chosen from calcium, magnesium, copper, zinc, iron, aluminum.
- the lamellar crystallites may comprise a mixture of at least two metals.
- the lamellar crystallites comprise a mixture of two metals, which preferably are zinc and copper.
- the quantity of lamellar crystallites dispersed in the aqueous lubricant during its use usually represents 0.1 to 5% by weight relative to the total weight lubricant when in use.
- the amount of lamellar crystallites is between 0.1 and 1% by weight relative to the same reference.
- the lamellar crystallites according to the invention can be used in presence of at least one nonionic surfactant.
- the number of polyoxyalkylene units, if present, of these nonionic surfactants usually varies from 2 to 100. It should be noted that, by polyoxyalkylenated units, the oxyethylenes, oxypropylene, or mixtures thereof.
- the surfactant content usually varies between 0 and 5% by weight total amount of lubricant when used.
- Lamellar crystallites can be obtained by contacting a solution or a dispersion comprising the acids possibly neutralized with the metal presenting in ionic and / or metallic form.
- dispersion we mean a dispersion of vesicles, droplets or micelles in an aqueous medium.
- a dispersion comprising at least one nonionic surfactant, such as in particular chosen from the list indicated previously.
- the surfactant content usually varies, in the case where it is present, between 1 and 30% by total weight of the concentrated dispersion.
- the latter may indifferently be under its metal form or in the form of a multivalent cation.
- Said cation can itself be find in the form of a solid, a solution or a dispersion.
- salts of mineral acids such as halides, with chlorides for example; nitrates, as well as salts organic acids such as formate, acetate, among others.
- metal in a form oxide, hydroxide, carbonate, or the metal itself.
- the contacting is carried out in the presence of at least one compound having the effect of buffering the pH.
- at least one compound having the effect of buffering the pH we choose one or several compounds such that the pH of the medium is between 7 and 9, preferably between 8 and 8.5.
- the contacting takes place with stirring.
- the metal under the chosen form in the solution or dispersion of the acids possibly neutralized by the aforementioned mineral or organic base.
- the operation is advantageously carried out at a temperature below 100 ° C., and preferably at a temperature between 20 and 60 ° C.
- the lamellar crystallites according to the invention are therefore used, and this constitutes a another object of the present invention, as an extreme-pressure additive in aqueous lubricants used for the deformation or transformation of metals.
- deformation is understood to mean in particular the drawing, rolling operations. Processing operations refer more specifically to cutting of metals.
- the metals which can be the subject of such treatments are in particular, and mainly, steels, stainless steels, aluminum, copper, zinc, tin, alloys based on copper (bronze, brass), etc.
- lubricants aqueous phase comprising the lamellar phases according to the invention are used in the drawing operations of brass-plated steel wires.
- Aqueous lubricants are generally colloidal dispersions in water. he It should be noted that the dispersions may be emulsions or dispersions solid particles or phases organized in an aqueous medium.
- Aqueous lubricants generally have a pH of between 7 and 9.
- They may further include conventional additives in this field, such as preservatives, anti-corrosion agents, anti-foam agents, stabilizing agents.
- the lamellar crystallites according to the invention can be indifferently introduced in a bath treatment or deformation of the metal, new or worn.
- the lamellar crystallites according to the invention can be introduced into the bath in the form of precursors. So we can add to the bath, on the one hand the solution of the possibly neutralized acids, and on the other hand, the metal in the form required.
- the resulting mixture is then diluted 10 times.
- Brass powder (15 g / l) was then added with stirring at 40 ° C.
- the mixture is left stirring for 5 days at the temperature indicated above.
- the figure shows indeed lamellar crystallites of section between 50 and 100 nm and longer than 2-3 ⁇ m (full scale of the figure: 2 ⁇ m).
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9913139 | 1999-10-21 | ||
| FR9913139A FR2800091B1 (fr) | 1999-10-21 | 1999-10-21 | Utilisation de micro-lamelles en tant qu'additifs extreme-pression dans des lubrifiants aqueux, micro-lamelles et leur obtention |
| PCT/FR2000/002944 WO2001029159A1 (fr) | 1999-10-21 | 2000-10-23 | Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1230331A1 EP1230331A1 (fr) | 2002-08-14 |
| EP1230331B1 true EP1230331B1 (fr) | 2005-04-06 |
Family
ID=9551181
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00971481A Expired - Lifetime EP1230331B1 (fr) | 1999-10-21 | 2000-10-23 | Utilisation de cristallites lamellaires en tant qu'additifs extreme-pression dans des lubrifiants aqueux, cristallites lamellaires et leur obtention |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6806238B1 (pt) |
| EP (1) | EP1230331B1 (pt) |
| JP (2) | JP2003528940A (pt) |
| KR (1) | KR100523717B1 (pt) |
| CN (1) | CN100345950C (pt) |
| AT (1) | ATE292668T1 (pt) |
| AU (1) | AU772577B2 (pt) |
| BR (1) | BR0014935B1 (pt) |
| CA (1) | CA2387820C (pt) |
| DE (1) | DE60019327T2 (pt) |
| ES (1) | ES2235968T3 (pt) |
| FR (1) | FR2800091B1 (pt) |
| MX (1) | MXPA02003685A (pt) |
| WO (1) | WO2001029159A1 (pt) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2820431B1 (fr) | 2001-02-06 | 2007-04-27 | Rhodia Chimie Sa | Procede de deformation de metaux mettant en oeuvre un lubrifiant aqueux additive permettant d'augmenter la productivite |
| KR100591778B1 (ko) * | 2005-01-19 | 2006-06-26 | 몽 필 김 | 곡물 분쇄기 |
| AT502630B1 (de) * | 2005-10-21 | 2008-01-15 | Miba Sinter Austria Gmbh | Bauelement, insbesondere formteil, mit einer beschichtung |
| US7449432B2 (en) * | 2006-03-07 | 2008-11-11 | Ashland Licensing And Intellectual Property, Llc (Alip) | Gear oil composition containing nanomaterial |
| GB201503566D0 (en) | 2015-03-03 | 2015-04-15 | Spheritech Ltd | Microparticles |
| CN106350190B (zh) * | 2016-08-19 | 2019-04-30 | 湖北省化学工业研究设计院 | 一种高强镀黄铜钢丝拉拔润滑剂及其制备方法 |
| WO2022099300A1 (en) | 2020-11-05 | 2022-05-12 | Ardagh Metal Beverage USA Inc. | Metalworking formulations with corrosion inhibitor formulations |
| KR102477036B1 (ko) | 2022-05-26 | 2022-12-19 | 주식회사 에스에이치엘 | 습식윤활액 조성물 |
| WO2026077848A1 (en) | 2024-10-10 | 2026-04-16 | Specialty Operations France | Lubricant composition |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3036118A (en) * | 1957-09-11 | 1962-05-22 | Wyandotte Chemicals Corp | Mixtures of novel conjugated polyoxyethylene-polyoxypropylene compounds |
| US4452711A (en) * | 1983-01-20 | 1984-06-05 | Aluminum Company Of America | Aqueous metalworking lubricant containing polyoxypropylene-polyoxyethylene-polyoxypropylene block copolymers |
| US5807810A (en) * | 1989-08-24 | 1998-09-15 | Albright & Wilson Limited | Functional fluids and liquid cleaning compositions and suspending media |
| GB8926885D0 (en) * | 1989-11-28 | 1990-01-17 | Albright & Wilson | Drilling fluids |
| US5964692A (en) * | 1989-08-24 | 1999-10-12 | Albright & Wilson Limited | Functional fluids and liquid cleaning compositions and suspending media |
| US6166095A (en) * | 1993-12-15 | 2000-12-26 | Albright & Wilson Uk Limited | Method of preparing a drilling fluid comprising structured surfactants |
| WO1995034694A1 (en) * | 1994-06-13 | 1995-12-21 | E.I. Du Pont De Nemours And Company | Corrosion inhibitor composition for steel |
| FR2758561B1 (fr) * | 1996-11-25 | 1999-04-23 | Rhodia Chimie Sa | Compositions d'orthophosphates soufres, leur procede de preparation et leur utilisation |
| JPH11279581A (ja) * | 1998-03-26 | 1999-10-12 | Kyodo Yushi Co Ltd | 金属加工用水溶性油剤 |
| FR2777902B1 (fr) * | 1998-04-28 | 2002-03-15 | Rhodia Chimie Sa | Utilisation dans un lubrifiant de trefilage,d'une suspension d'un sel de cobalt comme agent d'adherence,suspension et son obtention |
-
1999
- 1999-10-21 FR FR9913139A patent/FR2800091B1/fr not_active Expired - Fee Related
-
2000
- 2000-10-23 EP EP00971481A patent/EP1230331B1/fr not_active Expired - Lifetime
- 2000-10-23 CA CA002387820A patent/CA2387820C/fr not_active Expired - Fee Related
- 2000-10-23 DE DE60019327T patent/DE60019327T2/de not_active Expired - Lifetime
- 2000-10-23 MX MXPA02003685A patent/MXPA02003685A/es active IP Right Grant
- 2000-10-23 WO PCT/FR2000/002944 patent/WO2001029159A1/fr not_active Ceased
- 2000-10-23 AT AT00971481T patent/ATE292668T1/de not_active IP Right Cessation
- 2000-10-23 BR BRPI0014935-7A patent/BR0014935B1/pt not_active IP Right Cessation
- 2000-10-23 KR KR10-2002-7005010A patent/KR100523717B1/ko not_active Expired - Fee Related
- 2000-10-23 AU AU10330/01A patent/AU772577B2/en not_active Ceased
- 2000-10-23 US US10/111,002 patent/US6806238B1/en not_active Expired - Lifetime
- 2000-10-23 CN CNB008145687A patent/CN100345950C/zh not_active Expired - Lifetime
- 2000-10-23 ES ES00971481T patent/ES2235968T3/es not_active Expired - Lifetime
- 2000-10-23 JP JP2001531946A patent/JP2003528940A/ja active Pending
-
2009
- 2009-08-07 JP JP2009184750A patent/JP2009287030A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE60019327D1 (de) | 2005-05-12 |
| DE60019327T2 (de) | 2006-05-04 |
| BR0014935A (pt) | 2002-06-11 |
| KR20020052192A (ko) | 2002-07-02 |
| EP1230331A1 (fr) | 2002-08-14 |
| CN100345950C (zh) | 2007-10-31 |
| FR2800091B1 (fr) | 2005-01-28 |
| FR2800091A1 (fr) | 2001-04-27 |
| US6806238B1 (en) | 2004-10-19 |
| JP2003528940A (ja) | 2003-09-30 |
| BR0014935B1 (pt) | 2011-03-22 |
| CA2387820A1 (fr) | 2001-04-26 |
| AU772577B2 (en) | 2004-04-29 |
| JP2009287030A (ja) | 2009-12-10 |
| AU1033001A (en) | 2001-04-30 |
| MXPA02003685A (es) | 2003-10-14 |
| CA2387820C (fr) | 2007-05-01 |
| KR100523717B1 (ko) | 2005-10-26 |
| ATE292668T1 (de) | 2005-04-15 |
| CN1382203A (zh) | 2002-11-27 |
| ES2235968T3 (es) | 2005-07-16 |
| WO2001029159A1 (fr) | 2001-04-26 |
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