US20090036335A1 - Process for obtaining an intermetallic compound and use thereof in lubricating oils - Google Patents
Process for obtaining an intermetallic compound and use thereof in lubricating oils Download PDFInfo
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- US20090036335A1 US20090036335A1 US12/179,973 US17997308A US2009036335A1 US 20090036335 A1 US20090036335 A1 US 20090036335A1 US 17997308 A US17997308 A US 17997308A US 2009036335 A1 US2009036335 A1 US 2009036335A1
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- intermetallic compound
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- 239000010687 lubricating oil Substances 0.000 title claims abstract description 54
- 229910000765 intermetallic Inorganic materials 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims abstract description 44
- 230000008569 process Effects 0.000 title claims abstract description 30
- 239000000654 additive Substances 0.000 claims abstract description 23
- 229910052751 metal Inorganic materials 0.000 claims abstract description 21
- 239000002184 metal Substances 0.000 claims abstract description 21
- 230000000996 additive effect Effects 0.000 claims abstract description 16
- 230000001464 adherent effect Effects 0.000 claims abstract description 4
- 239000012798 spherical particle Substances 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 27
- 230000009467 reduction Effects 0.000 claims description 14
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical group [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 10
- 229910001337 iron nitride Inorganic materials 0.000 claims description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000002243 precursor Substances 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 239000000047 product Substances 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000012467 final product Substances 0.000 claims 1
- 239000000314 lubricant Substances 0.000 abstract description 24
- 239000003921 oil Substances 0.000 abstract description 14
- 230000005291 magnetic effect Effects 0.000 abstract description 5
- 150000002739 metals Chemical class 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 description 37
- 238000012360 testing method Methods 0.000 description 19
- 238000009472 formulation Methods 0.000 description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 238000006722 reduction reaction Methods 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 12
- 239000010439 graphite Substances 0.000 description 11
- 229910002804 graphite Inorganic materials 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 239000002270 dispersing agent Substances 0.000 description 8
- 238000012512 characterization method Methods 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 239000002199 base oil Substances 0.000 description 6
- 238000005461 lubrication Methods 0.000 description 6
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000012544 monitoring process Methods 0.000 description 4
- 238000011002 quantification Methods 0.000 description 4
- 239000002174 Styrene-butadiene Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- -1 for example Chemical class 0.000 description 3
- 238000000265 homogenisation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002086 nanomaterial Substances 0.000 description 3
- 239000002105 nanoparticle Substances 0.000 description 3
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- 208000032544 Cicatrix Diseases 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical group [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000010835 comparative analysis Methods 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 230000005294 ferromagnetic effect Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000386 microscopy Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 231100000241 scar Toxicity 0.000 description 2
- 230000037387 scars Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XAQHXGSHRMHVMU-UHFFFAOYSA-N [S].[S] Chemical compound [S].[S] XAQHXGSHRMHVMU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000016571 aggressive behavior Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 230000005293 ferrimagnetic effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000002751 molybdenum Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000010405 reoxidation reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Images
Classifications
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- 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
- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/20—Compounds containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/06—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron
- C01B21/0615—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron with transition metals other than titanium, zirconium or hafnium
- C01B21/0625—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron with transition metals other than titanium, zirconium or hafnium with copper
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/0828—Carbonitrides or oxycarbonitrides of metals, boron or silicon
-
- 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
- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/08—Metal carbides or hydrides
-
- 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
- C10M177/00—Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/44—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of magnetic liquids, e.g. ferrofluids
- H01F1/445—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of magnetic liquids, e.g. ferrofluids the magnetic component being a compound, e.g. Fe3O4
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/30—Particle morphology extending in three dimensions
- C01P2004/32—Spheres
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/12—Surface area
- C01P2006/13—Surface area thermal stability thereof at high temperatures
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- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/061—Carbides; Hydrides; Nitrides
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
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- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
- C10M2209/062—Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
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- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
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- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/16—Groups 8, 9, or 10
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- 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
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- 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
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- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
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- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/34—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials non-metallic substances, e.g. ferrites
Definitions
- the present invention relates to a process for obtaining an intermetallic compound having magnetic properties, utilised in the formulation of a finished lubricant and contributing to reduction in friction between metal surfaces of diverse dynamic systems. More particularly the compound of the present invention is formed by substantially-spherical nanoparticles having an extremely-active contact surface capable of forming a lubricating film on surfaces in contact in dynamic systems.
- Lubricating oils are fluid substances basically obtained by means of crude oil distillation. Lubricating oils may be classified as base lubricating oils or finished lubricating oils.
- Base lubricating oils may be of animal or vegetable origin, fatty oils group; derivatives of crude oil, mineral oils group; or be laboratory-produced, synthetic oils group.
- Mineral oils possess a chemical composition basically comprising paraffinic and naphthenic hydrocarbons. In some oils it is even possible to find traces of aromatic hydrocarbons, however traces of olefinic hydrocarbons are rarely found. Synthetic oils may also be composed of a mixture of two or more organic compounds such as, for example, polyalphaolefins, polyglycols, esters, silicones, among others, characterising the group of compound synthetic oils.
- Finished lubricating oils comprise products formulated commencing from base lubricating oils.
- the characteristic factor of a finished lubricant is the addition of a group of substances to the base lubricant permitting improvement of the quality of such base lubricating oil. Said substances are the so-called additives and may be solid or liquid.
- lubricating oil The function of lubricating oil is to reduce friction and wear of metal surfaces of equipment, and assist in cooling by heat exchange to protect dynamic systems against corrosion arising from oxidative processes.
- a film When lubricating oil is applied to a metal surface a very thin layer is formed, usually called a film. Said film is responsible for protecting moving surfaces of dynamic systems, acting in reducing friction and wear of said surfaces. The efficacy of protection is a factor dependent on the lubrication regime employed.
- a reactive film may be formed, formation whereof being due to action of the additives.
- Such reactive film formed improves even further the efficacy of the lubricant; there is an increase in resistance to wear and in reduction of friction occasioned by contact between moving metal surfaces of a dynamic system.
- solid additives may be added directly to the base lubricant.
- the best-known solid additives are: graphite, molybdenum disulphide (MoS 2 ) and polytetrafluoroethylene (TEFLON), whilst mica and talc may also be utilised as solid additives. These additives improve frictional efficacy between metal surfaces, particularly in situations of high load and impact.
- Graphite is usually utilised being an excellent lubricant due to its superlubrication effect. Said fact demonstrates that through the use of graphite as lubricant the frictional force of the material on which the graphite is applied practically disappears at a given moment.
- Graphite consists of carbon atoms disposed in superimposed layers forming an undulating crystalline structure.
- the lubricant action of graphite occurs due to sliding of the basal planes comprising the crystalline structure thereof.
- Molybdenum disulphide possesses characteristics appropriate for use in areas of extreme aggression such as, for example, deep water, military and aeronautical materials, chemical, petrochemical and petroleum-producing industries.
- This additive has a crystalline structure formed of extensive flat layers of molybdenum atoms disposed between layers of sulphur. Interactions between sulphur-sulphur planes are weak, leading to said layers sliding easily over one another.
- Molybdenum disulphide has good surface adherence due to the dry film formed thereon, excellent resistance to washout by water, excellent protection against corrosion, high resistance to continuous and intermittent extreme loads, and extended durability, permitting a longer working life for dynamic systems. These characteristics render this type of additive an excellent lubricant, principally at high temperatures.
- Polytetrafluoroethylene a product manufactured by the company DuPont and marketed under the brand TEFLON, is a material also usually utilised as an additive, the low shear force thereof giving rise to its lubricating activity. Its utilisation is limited due to the high cost of application thereof, in addition to the fact of solely being capable of utilisation within a specific band of temperature and load values, which fact limits its use.
- United States patent document US 2006094605 describes a process of obtaining a compound of molybdenum with sulphur and use of said compound as an additive for lubricants to reduce the coefficient of friction.
- nanoparticles of thiomolybdenum are produced by reacting acid salts in the presence of two modifying substances. Said process comprises homogenised heat treatment of the polar solvent of the mixture of molybdenum salt and one of such modifying substances. The mixture produced is cooled and then the second modifying substance is added.
- patent document WO 0127226 Another technology relating to lubricants is described in patent document WO 0127226. It describes a base lubricating oil for metals comprising 0.1 to 5% by weight of ferromagnetic or ferrimagnetic particles to subsequently be used having a volume weighted average crystallisation size ranging from 2 to 80 nm. The size of the nanoparticles formed determines a reduced contact surface area, limiting the efficacy of such lubricating oil.
- United States patent document US 2005124504 describes a lubricant composition comprising a nanomaterial and a dispersant of surfactant agent to promote stabilisation of the nanomaterial.
- the nanomaterial utilised in the lubricant composition described in said United States document is graphite.
- Graphite has high thermal conductivity, exceeding 80 W/m.
- Said lubricant composition is a fluid having unique properties, high heat conductivity, high viscosity index and small particles in suspension.
- the present invention comprises a process of obtaining an intermetallic compound having magnetic properties.
- Said intermetallic compound is a new additive for addition to a base lubricating oil, conferring high performance on said oil.
- the efficacy of the additive of the present invention consists in the reduction of friction between metal surfaces and reduction of wear of diverse types of dynamic system prolonging the working life thereof.
- the intermetallic compound of the present invention is formed of pulverised nanometric substantially-spherical particles having a high contact surface area, consequently being very active.
- the greater contact surface area of the substances forming part of the lubricant confers on said lubricant the capacity to accelerate the process of formation of a lubricant film.
- the lubricant formulated with this type of additive compound is capable of forming a thin layer, that is to say an adherent film, when applied to a metal surface, conferring thereon protection against friction and against wear.
- FIG. 1 shows a schematic drawing of the contact between the four spheres during the sliding test.
- FIG. 2 shows graphs of load against rotation obtained during the execution of the load cycles.
- the present invention relates to a process of obtaining an intermetallic compound having magnetic properties.
- Said compound acts as a solid additive and may be added to a base lubricating oil, creating a new finished lubricating oil.
- Such intermetallic compound of the present invention is capable of conferring high performance on the finished lubricating oil.
- the intermetallic compound herein disclosed contains within the molecular structure thereof species of the iron nitride and carbonitride type.
- the crystalline structure thereof is hexagonal, similar to the crystalline structure of graphite and of MoS 2 .
- Said compound is produced in pulverised form and the particles thereof are substantially spherical and nanometric.
- phase ⁇ is the crystalline phase which most contributes towards reduction of friction and of wear of metal surfaces of dynamic systems.
- the process of obtaining the intermetallic compound of the present invention comprises a first stage, consisting of a reduction reaction, followed by a second stage, consisting of a nitridation/carbonitridation reaction of a reaction precursor such as, for example, iron oxide, wherein the phenomenon of nucleation and formation of crystals of iron nitride and carbonitrides will occur.
- a reaction precursor such as, for example, iron oxide
- the iron oxide reduction reaction is realised in the presence of a reducing gas such as, for example, hydrogen, at high temperatures in a rotating-chamber reactor.
- a reducing gas such as, for example, hydrogen
- the temperature of the reaction system lies at approximately 800° C., at a reference rate of 30° C./min, preferentially the reaction temperature lies within a band from 300-800° C.
- the period of realisation of the reaction may subsist for up to approximately 10 hours, preferentially the reaction is realised within a range of 5-10 hours.
- the reaction system is subjected to the second stage of the process consisting in the nitridation/carbonitridation reaction, providing the system with nitrogen and carbon and the consequent formation of the crystals.
- Nitrogen and carbon are supplied to the reaction system through the addition of ammonia (NH 3 ) and methane (CH 4 ) to the reactor. This stage occurs at temperatures of approximately 800° C., preferentially in a band from 300-800° C. with a period of realisation which subsist for up to approximately 10 hours, preferentially the reaction is realised in a band of 1 to 6 hours.
- NH 3 ammonia
- CH 4 methane
- reaction system Following the period of realisation of the nitridation/carbonitridation reaction the reaction system must be cooled; cooling of the reaction system takes place to below a preferential temperature of approximately 25° C. The gas flow must be maintained during the cooling process to prevent oxidative degradation of the product, i.e. of the intermetallic compound.
- intermetallic compound formed of iron nitrides and carbonitrides it is subjected to characterisation by an appropriate characterisation technique.
- the characterisation technique utilised was scanning electronic microscopy showing that the intermetallic compound obtained is formed of substantially-spherical pulverised nanometric particles having a diameter of up to approximately 500 nm.
- the procedure of obtaining a finished lubricating oil containing the intermetallic product object of the present invention comprises the addition of said intermetallic compound to a solution composed of a base oil and a mixture of preferentially polymeric dispersants such as, for example, sulphonated dispersants or succimide dispersants.
- the dispersant acts on the mixture to prevent precipitation of said intermetallic compound or separation of the oil.
- Such tribological test comprised submitting said selected formulation to wear conditions by a suitable technique such as, for example, the sliding technique.
- Other types of lubricating oil were also submitted to the same test conditions.
- the lubricating oils utilised in said tribological test were: a base oil, the formulation of finished lubricating oil obtained by the present invention, a commercial finished lubricating oil and a mixture of a commercial lubricating oil with the metallic compound obtained in the present invention.
- the sliding technique realised in such tribological test comprises application of the diverse types of lubricating oils to suitable equipment such as, for example, equipment having four spheres operating under specific conditions developed during a load cycle.
- FIG. 1 shows the contact configuration for such spheres, that is to say the test specimens, disposed in equipment having four spheres.
- the equipment having four spheres operates with the three lower spheres affixed to a suitable device which also serves as a reservoir for the lubricating oil under evaluation.
- Said device may be, for example, a device of the sample-holder type.
- the fourth sphere is located in an upper position connected to a chuck disposed on a drive shaft which realises a rotational movement in a band from 150 to 1500 rpm, according to the phases realised during the load cycle.
- Said load cycle applied during the tribological test consists of three phases which, combined with the rotational movement of such driven shaft, cause wear of the spheres, in this manner permitting evaluation of the performance of the finished lubricating oil obtained in the present invention under different forms of lubrication.
- the temperature of the load cycle is controlled such that the formulation does not experience changes in regard to its degree of viscosity. Temperature control maintains the operation of the load cycle at approximately 90° C. The period of each load cycle realised in the sliding test is of approximately 60 minutes.
- Said evaluation consists of an average value obtained from the values of measurement of wear on such three spheres. Said average value is the final result of the tribological test of the different types of lubricating oil tested.
- reaction system was subjected to nitridation/carbonitridation reaction by the addition of a flow comprising NH 3 plus up to 20% by volume of CH 4 .
- said nitridation/carbonitridation reaction was processed at a preferential temperature of approximately 570° C. for a preferential period of approximately 5 hours.
- the reaction system was gradually cooled until the temperature reached room temperature.
- the procedure of cooling the reaction system occurred under an inert atmosphere to prevent reoxidation of the iron.
- Crystals of iron nitrides and carbonitrides comprise the solid additive, that is to say the intermetallic compound object of the present invention.
- the compound was subjected to characterisation by an appropriate characterisation technique.
- the characterisation technique utilised was scanning electronic microscopy, showing that the intermetallic compound obtained is formed of substantially-spherical pulverised nanometric particles having a preferential diameter lying in a band from 300 to 500 nm.
- Example 1 Approximately 10% of the intermetallic compound obtained in accordance with the procedure described in Example 1 was added to a solution comprising a base oil, in different concentrations, and a mixture of dispersants, preferably polymeric such as, for example, ethylene vinyl acetate (EVA) and styrene-butadiene (SBR) to prevent precipitation or separation of the oil.
- a mixture of polymeric dispersants comprised approximately 20% (EVA) and 20% (SBR).
- the concentration of said intermetallic compound in the diverse formulations obtained ranged from zero to 0.5%.
- the formulation containing the intermetallic compound at a concentration of 0.1% by weight was that yielding the best result in terms of power loss, being consequently selected for realisation of the tribological test.
- Said mixture of commercial finished oil with the intermetallic compound herein disclosed was obtained in a manner similar to the obtainment of the mixture of base oil with the intermetallic compound.
- the dispersant substances and the intermetallic compound were added to the commercial finished oil, subsequently being homogenised in a manner analogous to the mixture of base oil with the said compound.
- the different types of oil were applied separately to equipment having four spheres realising a rotational movement in a band from 150 to 15 000 rpm, according to the phases carried out during the load cycle.
- the lubricating oils analysed were subjected to a single load cycle.
- the load cycle applied during the tribological test consists of three phases which, combined with said rotational movement of the driving shaft, cause wear of said spheres and, consequently, evaluation of the performance of a lubricating oil under different forms of lubrication.
- the duration of the load cycle applied to the lubricating oils analysed is approximately 60 minutes and the temperature of the oil bath is controlled at a value of approximately 90° C.
- the first phase of said cycle occurs during a period of approximately 30 minutes.
- Such first phase of said load cycle operates under a hydrodynamic lubrication regime having a preferential rotational movement of 1500 rpm and a torque of approximately 98 N.
- the second phase of said load cycle occurs during a period of approximately 15 minutes.
- Such second phase of said load cycle operates under a mixed lubrication regime, that is to say the lubricant film may not permit contact between metal surfaces or sporadically permit contact between metal surfaces.
- Such second phase of said load cycle operates having a preferential rotational movement of 1500 rpm and a torque of approximately 1471 N.
- the conditions of the third phase of said load cycle are similar to those of the first phase, however the sole difference between said two phases relates to the level of torque applied.
- the torque applied is 147 N and the duration of such cycle is approximately 15 minutes.
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Abstract
The present invention relates to a process for obtaining an intermetallic compound having magnetic properties, added to a base lubricant to reduce friction between metal surfaces and reduce wear of diverse types of equipment prolonging the working life thereof. The intermetallic compound of the present invention is formed by pulverised nanometric substantially-spherical particles having an extremely active surface, capable of forming a thin adherent film when applied to a metal surface, conferring protection against frictional movements produced by contact between metals.
Said intermetallic compound is a new additive for addition to a base lubricating oil, conferring high performance on such oil.
Description
- The present invention relates to a process for obtaining an intermetallic compound having magnetic properties, utilised in the formulation of a finished lubricant and contributing to reduction in friction between metal surfaces of diverse dynamic systems. More particularly the compound of the present invention is formed by substantially-spherical nanoparticles having an extremely-active contact surface capable of forming a lubricating film on surfaces in contact in dynamic systems.
- Lubricating oils are fluid substances basically obtained by means of crude oil distillation. Lubricating oils may be classified as base lubricating oils or finished lubricating oils.
- Base lubricating oils may be of animal or vegetable origin, fatty oils group; derivatives of crude oil, mineral oils group; or be laboratory-produced, synthetic oils group.
- Mineral oils possess a chemical composition basically comprising paraffinic and naphthenic hydrocarbons. In some oils it is even possible to find traces of aromatic hydrocarbons, however traces of olefinic hydrocarbons are rarely found. Synthetic oils may also be composed of a mixture of two or more organic compounds such as, for example, polyalphaolefins, polyglycols, esters, silicones, among others, characterising the group of compound synthetic oils.
- Finished lubricating oils comprise products formulated commencing from base lubricating oils. The characteristic factor of a finished lubricant is the addition of a group of substances to the base lubricant permitting improvement of the quality of such base lubricating oil. Said substances are the so-called additives and may be solid or liquid.
- The function of lubricating oil is to reduce friction and wear of metal surfaces of equipment, and assist in cooling by heat exchange to protect dynamic systems against corrosion arising from oxidative processes.
- When lubricating oil is applied to a metal surface a very thin layer is formed, usually called a film. Said film is responsible for protecting moving surfaces of dynamic systems, acting in reducing friction and wear of said surfaces. The efficacy of protection is a factor dependent on the lubrication regime employed.
- According to the lubrication regime employed a reactive film may be formed, formation whereof being due to action of the additives. Such reactive film formed improves even further the efficacy of the lubricant; there is an increase in resistance to wear and in reduction of friction occasioned by contact between moving metal surfaces of a dynamic system.
- To obtain the finished lubricant solid additives may be added directly to the base lubricant. The best-known solid additives are: graphite, molybdenum disulphide (MoS2) and polytetrafluoroethylene (TEFLON), whilst mica and talc may also be utilised as solid additives. These additives improve frictional efficacy between metal surfaces, particularly in situations of high load and impact.
- Graphite is usually utilised being an excellent lubricant due to its superlubrication effect. Said fact demonstrates that through the use of graphite as lubricant the frictional force of the material on which the graphite is applied practically disappears at a given moment.
- Graphite consists of carbon atoms disposed in superimposed layers forming an undulating crystalline structure. The lubricant action of graphite occurs due to sliding of the basal planes comprising the crystalline structure thereof.
- However efficacy of the sliding process may be compromised due to resistance occasioned by coincidence of peaks of one layer with valleys of the adjacent layer occasioning perfect locking together of such superimposed layers, rendering the sliding thereof impossible.
- One manner of preventing resistance to the layers sliding is should two layers and be rotated one in relation to the other, in this manner there will be occasions wherein peaks of one layer touch the peaks of another layer. This fact prevents the two layers locking together such that sliding resistance practically disappears.
- The disadvantage of the use of graphite as lubricant stems from the greatest benefit from graphite occurring in humid atmospheres, which condition is not expected in the case of mediums with lubricating oils.
- Molybdenum disulphide possesses characteristics appropriate for use in areas of extreme aggression such as, for example, deep water, military and aeronautical materials, chemical, petrochemical and petroleum-producing industries. This additive has a crystalline structure formed of extensive flat layers of molybdenum atoms disposed between layers of sulphur. Interactions between sulphur-sulphur planes are weak, leading to said layers sliding easily over one another.
- Molybdenum disulphide has good surface adherence due to the dry film formed thereon, excellent resistance to washout by water, excellent protection against corrosion, high resistance to continuous and intermittent extreme loads, and extended durability, permitting a longer working life for dynamic systems. These characteristics render this type of additive an excellent lubricant, principally at high temperatures.
- However the negative aspects of the use of molybdenum disulphide consist in the fact that commercially this additive has been quoted at high prices, it has a high density, in addition it being a substance which it is difficult to stabilise in liquid mediums.
- Polytetrafluoroethylene, a product manufactured by the company DuPont and marketed under the brand TEFLON, is a material also usually utilised as an additive, the low shear force thereof giving rise to its lubricating activity. Its utilisation is limited due to the high cost of application thereof, in addition to the fact of solely being capable of utilisation within a specific band of temperature and load values, which fact limits its use.
- Finished lubricating oils together with additives added to a base lubricating oil for better performance thereof are topics extensively discussed in the literature.
- United States patent document US 2006094605 describes a process of obtaining a compound of molybdenum with sulphur and use of said compound as an additive for lubricants to reduce the coefficient of friction. In the process described in document US 2006094605 nanoparticles of thiomolybdenum are produced by reacting acid salts in the presence of two modifying substances. Said process comprises homogenised heat treatment of the polar solvent of the mixture of molybdenum salt and one of such modifying substances. The mixture produced is cooled and then the second modifying substance is added.
- Another technology relating to lubricants is described in patent document WO 0127226. It describes a base lubricating oil for metals comprising 0.1 to 5% by weight of ferromagnetic or ferrimagnetic particles to subsequently be used having a volume weighted average crystallisation size ranging from 2 to 80 nm. The size of the nanoparticles formed determines a reduced contact surface area, limiting the efficacy of such lubricating oil.
- Also comprising the state of the art, United States patent document US 2005124504 describes a lubricant composition comprising a nanomaterial and a dispersant of surfactant agent to promote stabilisation of the nanomaterial. The nanomaterial utilised in the lubricant composition described in said United States document is graphite. Graphite has high thermal conductivity, exceeding 80 W/m. Said lubricant composition is a fluid having unique properties, high heat conductivity, high viscosity index and small particles in suspension.
- The principal sectors of application of lubricating oil or lubricant compositions are the automotive, industrial, maritime and railway sectors.
- Consequently there is still not to be found described in the literature a finished lubricating oil composition having an additive providing efficient physicochemical properties making possible the high performance of such lubricating oil composition in the efficient reduction of friction and wear of metal surfaces of dynamic systems when in movement.
- The present invention comprises a process of obtaining an intermetallic compound having magnetic properties. Said intermetallic compound is a new additive for addition to a base lubricating oil, conferring high performance on said oil. The efficacy of the additive of the present invention consists in the reduction of friction between metal surfaces and reduction of wear of diverse types of dynamic system prolonging the working life thereof. More particularly the intermetallic compound of the present invention is formed of pulverised nanometric substantially-spherical particles having a high contact surface area, consequently being very active. The greater contact surface area of the substances forming part of the lubricant confers on said lubricant the capacity to accelerate the process of formation of a lubricant film. The lubricant formulated with this type of additive compound is capable of forming a thin layer, that is to say an adherent film, when applied to a metal surface, conferring thereon protection against friction and against wear.
-
FIG. 1 shows a schematic drawing of the contact between the four spheres during the sliding test. -
FIG. 2 shows graphs of load against rotation obtained during the execution of the load cycles. -
FIG. 3 shows the result of the tribological wear test on the lubricating oils tested. - The present invention relates to a process of obtaining an intermetallic compound having magnetic properties. Said compound acts as a solid additive and may be added to a base lubricating oil, creating a new finished lubricating oil. Such intermetallic compound of the present invention is capable of conferring high performance on the finished lubricating oil.
- The physicochemical properties of such intermetallic compound endow on the finished lubricant efficient performance in the reduction of friction between metal surfaces and in the reduction of wear in diverse types of dynamic systems prolonging the working life of equipments constituting said systems.
- The intermetallic compound herein disclosed contains within the molecular structure thereof species of the iron nitride and carbonitride type. The crystalline structure thereof is hexagonal, similar to the crystalline structure of graphite and of MoS2. Said compound is produced in pulverised form and the particles thereof are substantially spherical and nanometric.
- From among the crystalline phases constituting nitrides and carbonitrides, phase ε is the crystalline phase which most contributes towards reduction of friction and of wear of metal surfaces of dynamic systems. A further characteristic related to said phase ε, conferring efficacy on nitrides and carbonitrides, is the excellent corrosion resistance which this phase presents.
- The efficacy of the intermetallic compound obtained by the process of the present invention is also related with the magnetic properties of said compound. The intrinsic ferromagnetic property of the new intermetallic compound endows on the lubricating oil the capacity to form a thin adherent film when applied on a metal surface, conferring on said surface protection against frictional movements caused by contact between metals.
- The process of obtaining the intermetallic compound of the present invention comprises a first stage, consisting of a reduction reaction, followed by a second stage, consisting of a nitridation/carbonitridation reaction of a reaction precursor such as, for example, iron oxide, wherein the phenomenon of nucleation and formation of crystals of iron nitride and carbonitrides will occur.
- The iron oxide reduction reaction is realised in the presence of a reducing gas such as, for example, hydrogen, at high temperatures in a rotating-chamber reactor. During realisation of the reaction the temperature of the reaction system lies at approximately 800° C., at a reference rate of 30° C./min, preferentially the reaction temperature lies within a band from 300-800° C. The period of realisation of the reaction may subsist for up to approximately 10 hours, preferentially the reaction is realised within a range of 5-10 hours.
- Use of a rotating-chamber reactor for such reduction reaction promotes a high yield in terms of obtaining the product, this not being the case when carrying out said reaction in static-bed reactors.
- Following completion of the iron oxide reduction stage, the reaction system is subjected to the second stage of the process consisting in the nitridation/carbonitridation reaction, providing the system with nitrogen and carbon and the consequent formation of the crystals.
- Nitrogen and carbon are supplied to the reaction system through the addition of ammonia (NH3) and methane (CH4) to the reactor. This stage occurs at temperatures of approximately 800° C., preferentially in a band from 300-800° C. with a period of realisation which subsist for up to approximately 10 hours, preferentially the reaction is realised in a band of 1 to 6 hours.
- Following the period of realisation of the nitridation/carbonitridation reaction the reaction system must be cooled; cooling of the reaction system takes place to below a preferential temperature of approximately 25° C. The gas flow must be maintained during the cooling process to prevent oxidative degradation of the product, i.e. of the intermetallic compound.
- Having obtained said intermetallic compound formed of iron nitrides and carbonitrides it is subjected to characterisation by an appropriate characterisation technique. In the present embodiment the characterisation technique utilised was scanning electronic microscopy showing that the intermetallic compound obtained is formed of substantially-spherical pulverised nanometric particles having a diameter of up to approximately 500 nm.
- Following the obtaining and characterisation of such intermetallic compound, said compound was added to a base lubricating oil to then realise the tribological friction and wear evaluation test, the same showing the efficacy of the new additive herein proposed.
- The procedure of obtaining a finished lubricating oil containing the intermetallic product object of the present invention comprises the addition of said intermetallic compound to a solution composed of a base oil and a mixture of preferentially polymeric dispersants such as, for example, sulphonated dispersants or succimide dispersants. The dispersant acts on the mixture to prevent precipitation of said intermetallic compound or separation of the oil.
- Following addition of said intermetallic compound to said solution the mixture is subjected to homogenisation by a process of mechanical stirring in suitable equipment such as, for example, a Turrax-type mixer. With this type of stirring the particles experience strong collision. Such collision will promote controlled cavitation such that the size of the particles is reduced and they are dispersed and better distributed in solution. Stirring occurs within a preferential rotational band from 5000 to 25 000 rpm for a period preferentially lying within a band from 5 to 30 minutes. In this manner diverse formulations of the finished lubricating oil were obtained.
- Following obtaining such finished lubricating oil formulations, said formulations were initially analysed in respect of the frictional energy thereof and, in accordance with such initial results, one of said formulations was selected for realisation of the tribological test to evaluate the effect of addition of such new compound produced to a base lubricating oil.
- Such tribological test comprised submitting said selected formulation to wear conditions by a suitable technique such as, for example, the sliding technique. Other types of lubricating oil were also submitted to the same test conditions. The lubricating oils utilised in said tribological test were: a base oil, the formulation of finished lubricating oil obtained by the present invention, a commercial finished lubricating oil and a mixture of a commercial lubricating oil with the metallic compound obtained in the present invention.
- The sliding technique realised in such tribological test comprises application of the diverse types of lubricating oils to suitable equipment such as, for example, equipment having four spheres operating under specific conditions developed during a load cycle.
-
FIG. 1 shows the contact configuration for such spheres, that is to say the test specimens, disposed in equipment having four spheres. - The equipment having four spheres operates with the three lower spheres affixed to a suitable device which also serves as a reservoir for the lubricating oil under evaluation. Said device may be, for example, a device of the sample-holder type.
- The fourth sphere is located in an upper position connected to a chuck disposed on a drive shaft which realises a rotational movement in a band from 150 to 1500 rpm, according to the phases realised during the load cycle.
- Said load cycle applied during the tribological test consists of three phases which, combined with the rotational movement of such driven shaft, cause wear of the spheres, in this manner permitting evaluation of the performance of the finished lubricating oil obtained in the present invention under different forms of lubrication.
- The temperature of the load cycle is controlled such that the formulation does not experience changes in regard to its degree of viscosity. Temperature control maintains the operation of the load cycle at approximately 90° C. The period of each load cycle realised in the sliding test is of approximately 60 minutes.
- During realisation of each load cycle electronic files are generated by the data acquisition system of the equipment, permitting monitoring of frictional torque and quantification of frictional energy to which such spheres are subjected.
- On completion of such load cycle the lower spheres are evaluated. Said evaluation consists of an average value obtained from the values of measurement of wear on such three spheres. Said average value is the final result of the tribological test of the different types of lubricating oil tested.
- For the purpose of the present invention being better understood, the invention will be particularised hereinafter in the form of examples. However such examples herein described are of a purely illustrative nature and are not limitative of the invention.
- Obtaining the intermetallic compound.
- In a reactor provided with a rotating chamber there was added approximately 100 g of iron oxide in the form of powder in a hydrogen atmosphere. The average size of the particles of iron oxide added to such reactor ranged from 1 to 15 μm. The reaction was processed at a preferential temperature of approximately 700° C. for a preferential period of 7 hours.
- Following completion of the period of realisation of the reduction reaction, the reaction system was subjected to nitridation/carbonitridation reaction by the addition of a flow comprising NH3 plus up to 20% by volume of CH4.
- Following addition of NH3 and CH4, said nitridation/carbonitridation reaction was processed at a preferential temperature of approximately 570° C. for a preferential period of approximately 5 hours.
- Following completion of the period of realisation of the nitridation/carbonitridation reaction, the reaction system was gradually cooled until the temperature reached room temperature. The procedure of cooling the reaction system occurred under an inert atmosphere to prevent reoxidation of the iron. Crystals of iron nitrides and carbonitrides comprise the solid additive, that is to say the intermetallic compound object of the present invention.
- Having obtained said intermetallic compound formed of iron nitrides and carbonitrides, the compound was subjected to characterisation by an appropriate characterisation technique. In the present embodiment the characterisation technique utilised was scanning electronic microscopy, showing that the intermetallic compound obtained is formed of substantially-spherical pulverised nanometric particles having a preferential diameter lying in a band from 300 to 500 nm.
- Obtaining the finished lubricating oil containing the intermetallic compound of iron nitride and carbonitride herein produced.
- Approximately 10% of the intermetallic compound obtained in accordance with the procedure described in Example 1 was added to a solution comprising a base oil, in different concentrations, and a mixture of dispersants, preferably polymeric such as, for example, ethylene vinyl acetate (EVA) and styrene-butadiene (SBR) to prevent precipitation or separation of the oil. The mixture of polymeric dispersants comprised approximately 20% (EVA) and 20% (SBR). The concentration of said intermetallic compound in the diverse formulations obtained ranged from zero to 0.5%.
- Following addition of such intermetallic compound to said solution the mixture was subjected to homogenisation in a Turrax-type mixer at a preferential rotational speed of 15 000 rpm for a preferential period of 20 minutes.
- On completion of the period of homogenisation of such mixtures diverse formulations of finished lubricating oil were obtained. Said formulations were initially analysed in respect of the frictional energy thereof and in accordance with such initial results one of said formulations was selected for realisation of the tribological test for the evaluation of the effect of addition of such new additive produced to a base lubricating oil.
- Among such diverse formulations the formulation containing the intermetallic compound at a concentration of 0.1% by weight was that yielding the best result in terms of power loss, being consequently selected for realisation of the tribological test.
- Tribological test on the finished lubricating oil.
- Said tribological test consisted in the comparative analysis of diverse types of lubricating oil. Comparative analysis was carried out on a base oil, the formulation of finished lubricating oil obtained in accordance with the procedure described under Example 2, a commercial finished oil and a mixture of a commercial finished oil with the intermetallic compound obtained by means of the procedure described under Example 1.
- Said mixture of commercial finished oil with the intermetallic compound herein disclosed was obtained in a manner similar to the obtainment of the mixture of base oil with the intermetallic compound. The dispersant substances and the intermetallic compound were added to the commercial finished oil, subsequently being homogenised in a manner analogous to the mixture of base oil with the said compound.
- The different types of lubricating oils were subjected to conditions of wear by an appropriate technique such as, for example, the sliding technique. Such tribological test was realised in duplicate on all types of lubricating oil analysed.
- The different types of oil were applied separately to equipment having four spheres realising a rotational movement in a band from 150 to 15 000 rpm, according to the phases carried out during the load cycle. The lubricating oils analysed were subjected to a single load cycle.
- The load cycle applied during the tribological test consists of three phases which, combined with said rotational movement of the driving shaft, cause wear of said spheres and, consequently, evaluation of the performance of a lubricating oil under different forms of lubrication. The duration of the load cycle applied to the lubricating oils analysed is approximately 60 minutes and the temperature of the oil bath is controlled at a value of approximately 90° C.
- The first phase of said cycle occurs during a period of approximately 30 minutes. Such first phase of said load cycle operates under a hydrodynamic lubrication regime having a preferential rotational movement of 1500 rpm and a torque of approximately 98 N.
- The second phase of said load cycle occurs during a period of approximately 15 minutes. Such second phase of said load cycle operates under a mixed lubrication regime, that is to say the lubricant film may not permit contact between metal surfaces or sporadically permit contact between metal surfaces. Such second phase of said load cycle operates having a preferential rotational movement of 1500 rpm and a torque of approximately 1471 N.
- The conditions of the third phase of said load cycle are similar to those of the first phase, however the sole difference between said two phases relates to the level of torque applied. In the third phase of the load cycle the torque applied is 147 N and the duration of such cycle is approximately 15 minutes.
- During realisation of each load cycle electronic files are generated by the data acquisition system of the equipment to permit the monitoring of frictional torque and quantification of frictional energy to which such spheres were subjected. Said monitoring and quantification were accomplished by a spreadsheet produced in an operational program such as, for example, Excel. The graph generated for such monitoring and quantification is shown in
FIG. 2 . - On completion of each load cycle the lower spheres, being worn arising from contact with the upper sphere, were evaluated.
- Evaluation of said spheres was carried out by observing the presence of the wear mark on the external surface of the spheres. Said marks are called wear scars. The wear scars of each sphere were measured utilising an optical microscope and the average of said measurements performed on the three spheres yielded the final result of the tribological test on the lubricating oils tested, as shown in
FIG. 3 . - The invention herein described is not limited to this embodiment and those having ability in the art will perceive that any particular characteristic introduced therein shall solely be understood as something described to facilitate comprehension and cannot be realised without departing from the inventive concept described. The characteristics limiting the object of the present invention are listed in the claims forming part of this specification.
Claims (13)
1. Process for obtaining an intermetallic compound for reduction of friction on metal surfaces characterised in that the final product is an additive formed of pulverised nanometric substantially-spherical particles of iron nitrides and carbonitrides, having hexagonal crystalline structure, for addition to a base lubricating oil to provide efficacious performance in reduction of friction between metal surfaces and reduction of wear of diverse types of equipment, prolonging the working life thereof.
2. Process for obtaining an intermetallic compound according to claim 1 characterised in that the particles of such additive form an extremely-active surface, stable at high temperatures and forming a thin adherent film when applied to a metal surface.
3. Process for obtaining an intermetallic compound according to claim 1 characterised in that said process consists of a reaction of reduction and of formation of the product.
4. Process for obtaining an intermetallic compound according to claim 1 , characterised in that such reaction of reduction comprises a precursor and a reducing gas.
5. Process for obtaining an intermetallic compound according to claim 1 , characterised in that such precursor is iron oxide and the reducing gas is hydrogen.
6. Process for obtaining an intermetallic compound according to claim 1 , characterised in that said reaction occurs at temperatures of approximately 800° C., preferably in a temperature band from 300-800° C., in a rotating-chamber reactor for a period of up to 10 hours, preferentially in a period from 5-10 hours.
7. Process for obtaining an intermetallic compound according to claim 1 , characterised in that said reaction preferentially occurs at a temperature of 700° C. over a preferential period of 7 hours.
8. Process for obtaining an intermetallic compound according to claim 1 , characterised in that removal of oxygen occurs by addition of ammonia and methane to such reactor at temperatures of approximately 800° C., preferentially in a temperature band from 300-800° c., for a period of up to 10 hours, preferentially in a period from 1-6 hours.
9. Process for obtaining an intermetallic compound according to claim 1 , characterised in that such removal of oxygen occurs preferentially at a temperature of 570° C. over a preferential period of realisation of 5 hours.
10. Process for obtaining an intermetallic compound according to claim 1 characterised in that the reaction system is cooled to a preferential temperature of 25° C. and the flow of hydrogen gas is maintained constant.
11. Process for obtaining an intermetallic compound according to claim 1 , characterised in that the product obtained possesses a diameter of up to 500 nm.
12. Process for obtaining an intermetallic compound according to claim 1 , characterised in that such product obtained possesses a preferential diameter in a band from 300 to 500 nm.
13. Lubricating oil characterised in that it contains nanometric particles formed of iron nitrides and carbonitrides obtained by the process claimed in claim 1 .
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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BRPI0703141-6 | 2007-08-02 | ||
BRPI0703141A BRPI0703141B1 (en) | 2007-08-02 | 2007-08-02 | process of obtaining an intermetallic compound. |
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US20090036335A1 true US20090036335A1 (en) | 2009-02-05 |
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US12/179,973 Abandoned US20090036335A1 (en) | 2007-08-02 | 2008-07-25 | Process for obtaining an intermetallic compound and use thereof in lubricating oils |
Country Status (7)
Country | Link |
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US (1) | US20090036335A1 (en) |
EP (1) | EP2028255B1 (en) |
AR (1) | AR068312A1 (en) |
BR (1) | BRPI0703141B1 (en) |
CO (1) | CO6120164A1 (en) |
ES (1) | ES2734121T3 (en) |
PT (1) | PT2028255T (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2311926A1 (en) * | 2009-10-09 | 2011-04-20 | Rhein Chemie Rheinau GmbH | Additive for lubricant for improving the tribologic properties, a method for its production and application |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
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US5443662A (en) * | 1990-08-10 | 1995-08-22 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Method of forming a nitride or carbonitride layer |
US5985168A (en) * | 1997-09-29 | 1999-11-16 | University Of Pittsburgh Of The Commonwealth System Of Higher Education | Magnetorheological fluid |
US5998340A (en) * | 1997-03-07 | 1999-12-07 | Hitachi Maxell, Ltd. | Lubricant and magnetic recording medium using the same |
US20050124504A1 (en) * | 2002-07-26 | 2005-06-09 | Ashland Inc. | Lubricant and additive formulation |
US20050208320A1 (en) * | 2004-03-17 | 2005-09-22 | Kenji Masada | Iron nitride magnetic powder and method of producing the powder |
US20060094605A1 (en) * | 2002-10-23 | 2006-05-04 | Institut Neftekhimicheskogo Sinteza Ran Im. A.V. Topchieva (Inkhs Ran) | Method for producing lubricant additive (variants) |
US20100051850A1 (en) * | 2006-11-30 | 2010-03-04 | Petroleo Brasileiro S.A. - Petrobras | All in one magnetized intermetallic compound and lubricating oil |
Family Cites Families (8)
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GB1135812A (en) * | 1966-02-08 | 1968-12-04 | Ici Ltd | Production of iron nitride |
GB1499711A (en) * | 1976-12-10 | 1978-02-01 | Gkn Group Services Ltd | Nitriding |
JPS604901B2 (en) * | 1978-09-14 | 1985-02-07 | 日本スピンドル製造株式会社 | spinning ring |
DE19949032A1 (en) | 1999-10-12 | 2001-04-19 | Cognis Deutschland Gmbh | Lubricant for metal processing with ferromagnetic or ferrimagnetic nanoparticles |
NO20010929D0 (en) * | 2001-02-23 | 2001-02-23 | Norsk Hydro As | A method for conducting thermal reactions between reactants and an oven for the same |
JP3886968B2 (en) * | 2002-03-18 | 2007-02-28 | 日立マクセル株式会社 | Magnetic recording medium and magnetic recording cartridge |
EP1548760A3 (en) * | 2003-11-27 | 2007-12-26 | DOWA Electronics Materials Co., Ltd. | Iron nitride magnetic powder and method of producing the powder |
ES2403780T3 (en) * | 2003-11-28 | 2013-05-21 | Chevron Oronite S.A. | Composition of additive for transmission oil |
-
2007
- 2007-08-02 BR BRPI0703141A patent/BRPI0703141B1/en active IP Right Grant
-
2008
- 2008-05-15 AR ARP080102061A patent/AR068312A1/en unknown
- 2008-07-25 US US12/179,973 patent/US20090036335A1/en not_active Abandoned
- 2008-07-30 ES ES08252587T patent/ES2734121T3/en active Active
- 2008-07-30 PT PT08252587T patent/PT2028255T/en unknown
- 2008-07-30 CO CO08079291A patent/CO6120164A1/en not_active Application Discontinuation
- 2008-07-30 EP EP08252587.4A patent/EP2028255B1/en active Active
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5443662A (en) * | 1990-08-10 | 1995-08-22 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Method of forming a nitride or carbonitride layer |
US5998340A (en) * | 1997-03-07 | 1999-12-07 | Hitachi Maxell, Ltd. | Lubricant and magnetic recording medium using the same |
US5985168A (en) * | 1997-09-29 | 1999-11-16 | University Of Pittsburgh Of The Commonwealth System Of Higher Education | Magnetorheological fluid |
US20050124504A1 (en) * | 2002-07-26 | 2005-06-09 | Ashland Inc. | Lubricant and additive formulation |
US20060094605A1 (en) * | 2002-10-23 | 2006-05-04 | Institut Neftekhimicheskogo Sinteza Ran Im. A.V. Topchieva (Inkhs Ran) | Method for producing lubricant additive (variants) |
US20050208320A1 (en) * | 2004-03-17 | 2005-09-22 | Kenji Masada | Iron nitride magnetic powder and method of producing the powder |
US20100051850A1 (en) * | 2006-11-30 | 2010-03-04 | Petroleo Brasileiro S.A. - Petrobras | All in one magnetized intermetallic compound and lubricating oil |
Also Published As
Publication number | Publication date |
---|---|
BRPI0703141B1 (en) | 2018-10-16 |
PT2028255T (en) | 2019-08-01 |
EP2028255A1 (en) | 2009-02-25 |
EP2028255B1 (en) | 2019-06-12 |
BRPI0703141A2 (en) | 2009-03-17 |
AR068312A1 (en) | 2009-11-11 |
CO6120164A1 (en) | 2010-01-29 |
ES2734121T3 (en) | 2019-12-04 |
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