CS219105B1 - Lubricant with anticorrosion effects for electromechanical products - Google Patents
Lubricant with anticorrosion effects for electromechanical products Download PDFInfo
- Publication number
- CS219105B1 CS219105B1 CS807351A CS735180A CS219105B1 CS 219105 B1 CS219105 B1 CS 219105B1 CS 807351 A CS807351 A CS 807351A CS 735180 A CS735180 A CS 735180A CS 219105 B1 CS219105 B1 CS 219105B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- lubricant
- corrosion
- additive
- weight
- electromechanical components
- Prior art date
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- 239000000314 lubricant Substances 0.000 title claims abstract description 21
- 230000000694 effects Effects 0.000 title claims description 9
- 238000005260 corrosion Methods 0.000 claims abstract description 18
- 230000007797 corrosion Effects 0.000 claims abstract description 17
- 150000002148 esters Chemical class 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 13
- 239000012188 paraffin wax Substances 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 6
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 5
- 239000012964 benzotriazole Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 claims description 3
- -1 dicarboxylic acid ester Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical group O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 claims 1
- 238000000576 coating method Methods 0.000 abstract description 2
- 239000010970 precious metal Substances 0.000 abstract description 2
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 abstract description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000002704 decyl group Chemical group [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])* 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 10
- 230000001052 transient effect Effects 0.000 description 6
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 229940067597 azelate Drugs 0.000 description 4
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229950000688 phenothiazine Drugs 0.000 description 2
- GDWJVBGOLAZFIF-UHFFFAOYSA-N 1-phenylpyrazolidin-4-one Chemical compound C1C(=O)CNN1C1=CC=CC=C1 GDWJVBGOLAZFIF-UHFFFAOYSA-N 0.000 description 1
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 1
- WYVJDRGXWOXCCH-UHFFFAOYSA-N 5-methylpyrazolidin-3-one Chemical compound CC1CC(=O)NN1 WYVJDRGXWOXCCH-UHFFFAOYSA-N 0.000 description 1
- 101001109792 Homo sapiens Pro-neuregulin-2, membrane-bound isoform Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 102100022668 Pro-neuregulin-2, membrane-bound isoform Human genes 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 230000005226 mechanical processes and functions Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
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- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon only
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/30—Heterocyclic compounds
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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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/108—Phenothiazine
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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
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/32—Wires, ropes or cables 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/34—Lubricating-sealants
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
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- 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
- C10N2040/38—Conveyors or chain belts
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/40—Generators or electric motors in oil or gas winning field
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/42—Flashing oils or marking oils
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—Super vacuum or supercritical use
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- 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
- C10N2040/50—Medical uses
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Description
Vynález se týká . složení · lubrikantu pro elektromechanické součástky s antikorozními účinky, který umožňuje snížení tloušťky povlaku drahého kovu na . kontaktních plochách, značně zvyšuje korozní odolnost těchto součástek a prodlužuje jejich ' životnost tím, že omezuje mechanické opotřebení.The invention relates. the composition of a lubricant for electromechanical components with anticorrosive effects, which allows reducing the coating thickness of the precious metal to. contact surfaces greatly increases the corrosion resistance of these components and extends their service life by reducing mechanical wear.
Za elektromechanickou součástku je zde považována součástka využívaná pro spínání, spojování & rozpojování elektrického obvodu. Vykonává tedy vždy jistou mechanickou funkci a přenáší přitom elektrický proud, například konektor nebo přepínač.An electromechanical component here is considered to be a component used for switching, connecting & disconnecting an electrical circuit. Thus, it always performs a mechanical function and transmits electrical current, for example a connector or a switch.
V praxi je znáimo použití různých látek snižujících tření a omezujících korozi elektromechanických součástek. Využívá se k tomu obvykle minerálních olejů, solí a esterů mastných kyselin a dikariboxylových kyselin atd. Tyto· látky se obvykle kombinují s látkami slabil· ziačními, případně· s látkami! s antikorozním působením. Ke stabilizaci se používá obvykle látek typu fencthiazinu nebo substituovaného fenolu. Tyto směsi však většinou působí pouze mechanicky a nemají antikorozní účinky za' podmínek zkoušení elektromechanických součástek. To platí i o radě látek, které se v jiných oblastech . . úspěšně. · používají Jako .. .inhibitory koroze.In practice, it is known to use a variety of friction reducing and corrosion reducing agents for electromechanical components. Usually mineral oils, salts and esters of fatty acids and dicariboxylic acids, etc. are used for this purpose. These substances are usually combined with weakening substances or substances! with anticorrosive effect. Usually, the phenothiazine or substituted phenol type is used for stabilization. However, these mixtures generally act only mechanically and do not have corrosion effects under the test conditions of electromechanical components. This also applies to a number of substances that are in other areas. . successfully. Use as corrosion inhibitors.
Měření ukázala, že látky obvykle používané ke stabilizaci lubrikantů ' ' i · některé látky všeobecně používané jako inhibitory koroze naopak korozi silně urychlují, zejména při provádění korozních zkoušek s čistými látkami bez přítomnosti vlastních lubrlikantů, které jejich korozní působení do značné míry překrývají a to se potom projeví až za extrémních podmínek. Dobrou stabilitu lubrikantu je dle tohoto vynálezu zabezpečit i ve směsích obsahujících pouze látky, které mají za podmínek zkoušení a použití elektromechanických součástek výrazně inhťbiční účinky na korozi.Measurements have shown that substances commonly used to stabilize lubricants and some substances commonly used as corrosion inhibitors, on the contrary, strongly accelerate corrosion, especially when conducting corrosion tests with pure substances without the presence of intrinsic lubricants which largely overlap their corrosion action, then manifest under extreme conditions. According to the invention, good lubricant stability is also assured in mixtures containing only substances which, under the conditions of testing and use of electromechanical components, have markedly inhibitory corrosion effects.
Nevýhody dříve používaných lubrikantů jsou odstraněny směsí podle vynálezu obsahující pouze látky s význačným antikorozním působením, která míi přitom dobrou stabilitu a je zvláště vhodná pro elektromechanické součástky pokryté zcela nebo zčásti povlakem kovu ušlechtilejšího, než je základní materiál součástky, nebo 'materiál použité mezivrstvy. Měření prokázala, že zejména kombinací dvou inhibitorů koroze různých typů se podstatně zvyšuje antikorozní působení.The disadvantages of the lubricants previously used are eliminated by the composition according to the invention containing only substances with a significant anti-corrosion effect, which at the same time has good stability and is particularly suitable for electromechanical parts covered wholly or partially with a nobler metal than the base material or interlayer material. Measurements have shown that especially by combining two corrosion inhibitors of different types, the anticorrosive effect is substantially increased.
Lubrikainit je·v podstatě tvořen esterem dikarboxylové kyseliny, která má 5 až 12 atomů uhlíku v molekule -a · její ester celkem 20 až 28 atomů uhlíku v molekule, s přídavkem látky. . ze skupiny . pyrazolidcnu . v . .koncentraci 0,01 až 1 % hmot., která vyhovuje jedné ze tří možných struktur:Lubricinite consists essentially of a dicarboxylic acid ester having 5 to 12 carbon atoms in the molecule and its ester having a total of 20 to 28 carbon atoms in the molecule, with the addition of a substance. . from the group. pyrazolidine. v. a concentration of 0,01 to 1% by weight, which satisfies one of the three possible structures:
kde Ri až Rs je metyl nebo fenyl, nebo H.wherein R 1 to R 5 is methyl or phenyl, or H.
Směs může .dále obsahovat přísadu parafinu, který mění mechanické vlastnosti lubrikaintu a. přísadu benzotriazolu nebo tolyltriazolu.The composition may further comprise an additive of paraffin which alters the mechanical properties of the lubricant and an additive of benzotriazole or tolyltriazole.
K praktickému odzkoušení lubrikantů podle vynálezu byly připraveny směsi o složení uvedeném v příkladech 1 až 9. Píro porovnání antikorozních účinků byly připraveny další směsi obsahující často používané antloxidanty (příklad 10 .až 11), v dalších směsích . jsou tyto látky v kombinaci s jinými látkami často používanými jako inhibitory koroze (příklad 12 až 13).For practical testing of the lubricants of the invention, compositions having the compositions shown in Examples 1 to 9 were prepared. Further compositions containing frequently used antloxidants (Examples 10-11) were prepared for comparing the anticorrosive effects, in other compositions. they are in combination with other agents frequently used as corrosion inhibitors (Examples 12-13).
Příklad 1 di-3,5,5 triímetyl azelát 84% hmot.EXAMPLE 1 Di-3,5,5 Triethyl Azelate 84 wt.
(1 -fenyl^-pyrazolidon 1 % hmot parafin 15 % hmot.(1-phenyl-4-pyrazolidone 1 wt.% Paraffin 15 wt.
dioktylsebakát 98,9 % --metyl^-pyrazolidon 1 · % tolyKriazol 0,1 %dioctyl sebacate 98.9% - methyl-4-pyrazolidone 1 ·% tolyCriazole 0.1%
Příklad 3Example 3
Bis-2~-eh'ylliexyladipát 93,9 % l-fenyl-5-;metyl-3-pyrazxlidon 1 % benzotriazol 0,1 % parafin . 5 %Bis-2-methylhexyl adipate 93.9% 1-phenyl-5-methyl-3-pyrazxlidone 1% benzotriazole 0.1% paraffin. 5%
P r í k 1 a! -1 4 d1-3,5,5-trimethylhexyl azelát 99 % l-fenyl-S-imetyl^-pyrazolidon 1 % benzotriazol 10_4 одExample 1! -1 4 d -1-3,5,5-trimethylhexyl azelate 99% 1-phenyl-S-imethyl-4-pyrazolidone 1% benzotriazole 10 _ 4 од
Příklad 5 dioktylsebakát 99,5 %Example 5 Dioctyl sebacate 99.5%
5-metyl-3-pyrazo>lidoin 0,5 %5-methyl-3-pyrazole lidoin 0.5%
Příklad 6 dioktylsebakát 99,99 °/oExample 6 Dioctyl sebacate 99.99%
5-'mietyl-3-pyrazolidon 0,01 °/o5-Methyl-3-pyrazolidone 0.01%
Příklad 7 di-3,5,5-trimethylhexyl azelát 99,49 % l-feinyl-3-pyrazolidon 0,01 % tolyiltriazol 0,5 %Example 7 di-3,5,5-trimethylhexyl azelate 99.49% 1-phenynyl-3-pyrazolidone 0.01% tolyiltriazole 0.5%
Příklad 8 •di-3,5,5 tirimiethythexyl azelát 99 % 5-Tnietyl-3-py>r>a!ZOlidon 1 % bcinizo.rjazol 10r 4 %EXAMPLE 8 • Di-3,5,5-thiimethylethexyl azelate 99% 5-Triethyl-3-pyrazolone 1% bcinisoljazol 10% 4 %
P ř í к 1 a d 9 ,ďoktyl dcdekandiát 59 % l-fenyl-3-pyrazolidon 1 % parafin 40 %EXAMPLE 1, Doctyl dcdecandiate 59% 1-Phenyl-3-pyrazolidone 1% Paraffin 40%
Příklad 10 dibktyliadipált 58 %Example 10 dibktyliadipalt 58%
2,6i-dite'rc.butyl-4-'meitylfenol 1 % l-fenyl-3-pyrazolidoin 1 % parafin 40 °/o2,6-Di-tert-butyl-4-methyl-phenol 1% 1-phenyl-3-pyrazolidoin 1% paraffin 40%
Příklad 11 dioktyladipát 93 %Example 11 dioctyl adipate 93%
2.6- dite|rc.butyl-4-metylfenol 1 °/o l-fenyl-3-py'razol:don 1 % parafin 5 %2.6- child | tert-butyl-4-methylphenol 1% -1-phenyl-3-pyrazole: don 1% paraffin 5%
Příklad 12 dioktylsebakát 98 %Example 12 Dioctyl sebacate 98%
2.6- diiterc.butyl-4metyIfenol .1 % oktadecylamin 1 °/o2,6-di-tert-butyl-4-methylphenol. 1% octadecylamine 1% w / w
Příklad 13 di-3,5,5-tirii'met|liylhexyl.azelát 98 % fcnothiazin 1 % trietanioilamin 1 %Example 13 di-3,5,5-tirii'met | liylhexyl azlate 98% Phenothiazine 1% triethanioilamin 1%
Ve všech uvedených příkladech bylo složení zaokrouhlováno na setiny procenta.In all the examples, the composition was rounded to hundredths of a percent.
Všechny připravené směsi byly zkoušeny za stejných podmínek. Jako kritérium korozní lodoiinosti bylo použdo .měření přechodového odporu kontaktů po zkoušce v sirovodíkové atmosféře, která je obvyklou zkouškou píro tento druh součástek. Lubrikanty byly na kontakty naneseny ze 4% roztoku v xylenu. Pro zkoušky bylo použito kontaktů s vnější kontaktní plochou nepřímého řadového konektoru s kruhovými kontakty s přibližně 0,,25 mikrometry zlata v kontaktní části. Kontakty byly po usušení při teplotě 60 °C namontovány do příslušných tělísek. Odpovídající zásuvky se zlacenými kontakty byly použity pouze pro měření .a nebyly podrobeny korozní zkoušce. Po změření počátečního· přechodového odporu byly vdlice vlaženy do sirovodíku o koncentraci 1 % objemové při relativní vlhkosti 95 % o tepjoíš 25 °C na dobu 48 hodin a opět byl změřen přechodový odpor.All prepared mixtures were tested under the same conditions. As a corrosion test, a contact resistance measurement after the test in a hydrogen sulphide atmosphere, which is the usual test for this kind of components, was used. Lubricants were applied to the contacts from a 4% solution in xylene. Contacts with an outer contact surface of an indirect row connector with circular contacts with approximately 0.25 micrometers of gold in the contact portion were used for the tests. The contacts were mounted in the appropriate bodies after drying at 60 ° C. Corresponding gold-plated contact sockets were used for measurements only and were not subjected to corrosion testing. After measuring the initial transient resistance, the wells were pulled into 1% by volume hydrogen sulfide at 95% relative humidity at 25 ° C for 48 hours and the transient resistance was again measured.
.Pro každý vzorek by i o použito 30 kontaktů a z průměrných naměřených hodnot bylo vypočteno procentické zvýšení přechodového odporu po korozní zkoušce. Každý kontakt byl měřen 5krát. Výsledky jsou obsaženy v tabulce 1. Z výsledků je patrno, že lubrikanty dle vynálezu (1 až 9) poskytují nejlepší výsledky. Pro srovnání byla provedena stejná zkouška i s kontakty 'bez lubrikantu, v tabulce je tato skupina označena jako „0“’.30 contacts would be used for each sample and the percent increase in transient resistance after the corrosion test was calculated from the average values measured. Each contact was measured 5 times. The results are shown in Table 1. The results show that the lubricants of the invention (1 to 9) provide the best results. For comparison, the same test was performed with 'no lubricant contacts', in the table, this group is marked '0'.
К demonstraci dlouhodobé stability lubrikiantu dle tohoto vynálezu byla stejná zkouška provedena i po dlouhodobém zahřívání (56 dní) kontaktů opatřených lubrikanty na teplotu 100 °C. Výsledky jsou rovněž v tabulce a jsou v dobré shodě s předešlými, lubrikanty podle vynálezu opět poskytují nejlepší antikorozní ochranu. Hodnoty zvýšení přechodového odporu jsou ve všech případech poněkud vyšší vlivem vyšší náročnosti provedené zkoušky.To demonstrate the long-term stability of the lubricant of the present invention, the same test was performed after long-term heating (56 days) of the lubricated contacts to 100 ° C. The results are also in the table and are in good agreement with the foregoing, the lubricants of the invention again provide the best corrosion protection. The values of increase of the transient resistance are in all cases somewhat higher due to higher demands of the performed test.
Lubrikant 0Lubricant 0
Tabulka 1Table 1
5 6 7 ld 11.5 6 7 ld
1313
Ki (%) 84 27 18 11 15 42 51 38 38 25 128 68 92 140Ki% 84 27 18 11 15 42 51 38 38 25 128 68 92 140
K2 ('%) 121 35 23 20 23 54 62 48 51 31 181 111 Ϊ51 158K 2 ('%) 121 35 23 20 23 54 62 48 51 31 181 111 51 51 158
Ki je zvýšení přechodového odporu v pro- Кг je zvýšení přechodového odporu po centech po 48 hodinách v sirovodíkové at- 56 dnech zahřívání na 100 °C a 48 hodinách mosféře v sirovodíkové atmosféře vyjádřené v procentech.Ki is the increase in transient resistance in pro- cog is the increase in transient resistance in cents after 48 hours in hydrogen sulphide and 56 days of heating to 100 ° C and 48 hours in hydrogen sulphide atmosphere expressed as a percentage.
Claims (3)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS807351A CS219105B1 (en) | 1980-10-30 | 1980-10-30 | Lubricant with anticorrosion effects for electromechanical products |
| DD81233448A DD210549A3 (en) | 1980-10-30 | 1981-09-21 | FAT FOR ELECTROMECHANIC PARTS WITH ANTI-STRENGTH EFFECT |
| FR8118343A FR2493335A1 (en) | 1980-10-30 | 1981-09-29 | LUBRICANT FOR ELECTROMECHANICAL ELEMENTS WITH ANTI-CORROSION ACTION |
| GB8131872A GB2086418B (en) | 1980-10-30 | 1981-10-22 | Lubricant having anticorrosive properties for electro-mechanical components |
| CH6893/81A CH648589A5 (en) | 1980-10-30 | 1981-10-28 | LUBRICANTS FOR ELECTROMECHANICAL COMPONENTS WITH ANTICORROSIVE EFFECT. |
| DE19813143185 DE3143185A1 (en) | 1980-10-30 | 1981-10-30 | LUBRICANTS WITH ANTICORROSIVE EFFECT FOR ELECTROMECHANICAL COMPONENTS |
| HU359081A HU188558B (en) | 1980-10-30 | 1981-11-30 | Composition of protection of corrosion for sparing electric contacts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS807351A CS219105B1 (en) | 1980-10-30 | 1980-10-30 | Lubricant with anticorrosion effects for electromechanical products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS219105B1 true CS219105B1 (en) | 1983-02-25 |
Family
ID=5422494
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS807351A CS219105B1 (en) | 1980-10-30 | 1980-10-30 | Lubricant with anticorrosion effects for electromechanical products |
Country Status (6)
| Country | Link |
|---|---|
| CH (1) | CH648589A5 (en) |
| CS (1) | CS219105B1 (en) |
| DD (1) | DD210549A3 (en) |
| DE (1) | DE3143185A1 (en) |
| FR (1) | FR2493335A1 (en) |
| GB (1) | GB2086418B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4529531A (en) * | 1984-02-22 | 1985-07-16 | Stauffer Chemical Company | Electrical contact lubricant composition and method of lubrication |
| EP1574546A3 (en) * | 1996-05-10 | 2006-03-01 | Shishiai-Kabushikigaisha | Energy conversion composition |
| US10998730B1 (en) | 2019-04-26 | 2021-05-04 | NeoVolta, Inc. | Adaptive solar power battery storage system |
-
1980
- 1980-10-30 CS CS807351A patent/CS219105B1/en unknown
-
1981
- 1981-09-21 DD DD81233448A patent/DD210549A3/en not_active IP Right Cessation
- 1981-09-29 FR FR8118343A patent/FR2493335A1/en active Pending
- 1981-10-22 GB GB8131872A patent/GB2086418B/en not_active Expired
- 1981-10-28 CH CH6893/81A patent/CH648589A5/en not_active IP Right Cessation
- 1981-10-30 DE DE19813143185 patent/DE3143185A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| DE3143185A1 (en) | 1982-06-16 |
| FR2493335A1 (en) | 1982-05-07 |
| GB2086418B (en) | 1984-03-21 |
| DD210549A3 (en) | 1984-06-13 |
| CH648589A5 (en) | 1985-03-29 |
| GB2086418A (en) | 1982-05-12 |
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