HU198519B - Self-lubricating anti-friction mixture - Google Patents
Self-lubricating anti-friction mixture Download PDFInfo
- Publication number
- HU198519B HU198519B HU853699A HU369985A HU198519B HU 198519 B HU198519 B HU 198519B HU 853699 A HU853699 A HU 853699A HU 369985 A HU369985 A HU 369985A HU 198519 B HU198519 B HU 198519B
- Authority
- HU
- Hungary
- Prior art keywords
- density
- weight
- viscosity
- polyamide
- lubricating
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 55
- 238000005260 corrosion Methods 0.000 claims abstract description 35
- 230000007797 corrosion Effects 0.000 claims abstract description 34
- 239000003112 inhibitor Substances 0.000 claims abstract description 30
- 229920002647 polyamide Polymers 0.000 claims abstract description 24
- 239000004952 Polyamide Substances 0.000 claims abstract description 23
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000010687 lubricating oil Substances 0.000 claims abstract description 16
- 239000010439 graphite Substances 0.000 claims abstract description 11
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 11
- -1 alkenyl butanedioic anhydride Chemical compound 0.000 claims description 14
- 230000001603 reducing effect Effects 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- 239000002480 mineral oil Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 239000000314 lubricant Substances 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 235000010446 mineral oil Nutrition 0.000 claims description 6
- 239000003208 petroleum Substances 0.000 claims description 6
- 239000003365 glass fiber Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 4
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000007859 condensation product Substances 0.000 claims description 3
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical class C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 claims description 2
- 239000005642 Oleic acid Substances 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 abstract description 16
- 239000007788 liquid Substances 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- 239000007791 liquid phase Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000003792 electrolyte Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920002545 silicone oil Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 230000008014 freezing Effects 0.000 description 3
- 229920002959 polymer blend Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000010962 carbon steel Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- BDDLHHRCDSJVKV-UHFFFAOYSA-N 7028-40-2 Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O BDDLHHRCDSJVKV-UHFFFAOYSA-N 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical group [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000008430 aromatic amides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- FHYCJCVXLROHOO-UHFFFAOYSA-N diethyl(dihexadecyl)azanium;nitrate Chemical compound [O-][N+]([O-])=O.CCCCCCCCCCCCCCCC[N+](CC)(CC)CCCCCCCCCCCCCCCC FHYCJCVXLROHOO-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical class NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229940023462 paste product Drugs 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229940058401 polytetrafluoroethylene Drugs 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 150000003346 selenoethers Chemical class 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/048—Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution, non-macromolecular and macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/40—Lubricating compositions characterised by the base-material being a macromolecular compound containing nitrogen
- C10M107/44—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C10M125/02—Carbon; Graphite
-
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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
- 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
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- 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
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M133/10—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms cycloaliphatic
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- 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
- C10M133/16—Amides; Imides
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- 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
- C10M133/16—Amides; Imides
- C10M133/18—Amides; Imides of carbonic or haloformic acids
- C10M133/20—Ureas; Semicarbazides; Allophanates
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- 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
- C10M133/30—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms containing a nitrogen-to-oxygen bond
- C10M133/32—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms containing a nitrogen-to-oxygen bond containing a nitro group
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- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/02—Polyethene
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- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
- C10M143/04—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing propene
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- C10M147/00—Lubricating compositions characterised by the additive being a macromolecular compound containing halogen
- C10M147/02—Monomer containing carbon, hydrogen and halogen only
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/02—Natural products
- C10M159/04—Petroleum fractions, e.g. tars, solvents
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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- 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
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
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- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
- C10M2201/042—Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/104—Aromatic fractions
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/106—Naphthenic fractions
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
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Abstract
Description
A találmány tárgya önkenő súrlódáscsökkentő keverék.The present invention relates to a self-lubricating friction reducing composition.
A találmány tárgya közelebbről polimer keverék, önkenő súrlódáscsökkentő készítmény céljából. A találmány szerinti készítmények kenés nélkül csúszóalkatrészek, például csúszó csapágyak előállításánál, valamint ezek korlátozott (időszakos), szereléskor egyszeri, illetve javításkor periodikus használatánál alkalmazható.More particularly, the present invention relates to a polymer blend for self-lubricating friction reducing composition. The compositions of the invention can be used in the manufacture of non-lubricated sliding components such as sliding bearings, as well as in their limited (intermittent), one-off assembly or periodic use during repair.
Polimerek tiszta formában nem alkalmazhatók csúszóalkatrészek előállításához, mivel nem elégítik ki a csúszócsapágyak, mozgó tömítések és más alkatrészek megbízhatóságával és élettartamával szemben támasztott követelményeket. Ez a polimerek atmoszférikus körülmények között mutatott, relatív alacsony kopásállóságának és stabilitásának tudható be. A csúszóalkatrészek gyakran korrozív közegben dolgoznak, ami károsítja a fémalkatrészek, valamint a megnövekedett kopás következtében a polimerből készült összekapcsolt súrlódó helyek felszínét. Hasonló károsodásjelentkezik összekapcsolt polimer alkatrészekből és femalkatrészekből álló gépek és berendezések hosszabb időn keresztül történő tárolásánál is. Ebben az esetben a korrózió feszültségeket okoz az alkatrészben, amely üzem közben roncsolódáshoz vezethet.Polymers in pure form cannot be used for the manufacture of sliding parts because they do not meet the requirements for the reliability and service life of sliding bearings, moving seals and other parts. This is due to the relatively low abrasion resistance and stability of the polymers under atmospheric conditions. The sliding parts often work in corrosive media, which damages the surface of the metal parts and, due to the increased wear, the friction points of the polymer. Similar damage occurs when storing machines and equipment consisting of interconnected polymer parts and metal parts over an extended period of time. In this case, the corrosion will cause tension in the component, which can lead to failure during operation.
A 3 726 945. számú USA-beli szabadalmi leírásból ismert egy önkenő súrlódáscsökkentő keverék, amely 70-99,9 t% poliamidból és 0,1 - 30 tömeg% polioleflnből áll. Súrlódás hatására az alkatrész felületén a keverékből poliolefin-olvadék film keletkezik, amely csökkenti a súrlódási együtthatót és növeli a kopásállóságot. Ez a hatás azonban csak nagy igénybevételeknél és sebességeknél lép fel. A keverék ezenkívül nem biztosítja a korrózióelleni védelmet, ha az alkatrészt agresszív közegben kell alkalmazni.U.S. Pat. No. 3,726,945 discloses a self-lubricating friction reducing composition comprising 70-99.9% by weight of polyamide and 0.1-30% by weight of polyolefin. Friction results in the formation of a polyolefin melt film on the surface of the component, which reduces the coefficient of friction and increases wear resistance. However, this effect occurs only at high loads and speeds. In addition, the mixture does not provide anti-corrosion protection when the component is to be used in an aggressive medium.
Az 531 831. számú szovjet szabadalmi leírás olyan önkenő súrlódáscsökkentő keveréket ismertet, amely 100 tömegrész poliamidból áll. Ez a keverék alkalmas olyan súrlódó alkatrészek előállítására, amelyek védve vannak a környezet behatásai (nedvesség, napsugár, stb.) ellen, és viszonylag alacsony hőmérsékleten (legfeljebb 100 °C)' dolgoznak. Túlterhelések és nem stabilizált súrlódási körülmények következtében helyi túlmelegedések jelentkezhetnek, amely aktiválja a polimer anyagok lebomlását és oxidációját, amely az alkatrész gyorsított elöregedéséhez és idő előtti széteséshez vezet.U.S. Patent No. 531,831 discloses a self-lubricating friction reducing composition comprising 100 parts by weight of polyamide. This mixture is suitable for the production of frictional components which are protected against environmental influences (humidity, sunlight, etc.) and operate at relatively low temperatures (up to 100 ° C). Overloads and unstabilized friction conditions can result in local overheating, which activates the degradation and oxidation of polymeric materials, leading to accelerated component aging and premature disintegration.
A 704 958. számú szovjet szabadalmi leírás poliamid alapú önkenő súrlóaáscsökkentő készítményt ismertet, amely 10—15 tömeg% kenőolajból, 10—15 tömegé politetra fluor-etilén száraz kenőanyagból és 0,5-0,7 tömeg% etilénamin-tetraecetsavból áll. A keverék magas fizikai-mechanikai jellemzőkkel, magas kopásállósággal és alacsony súrlódási együtthatóval rendelkezik. Magas hőmérsékletek (100 *C felett) hatására azonban hosszabb idő után romlanak a fizikal-mechanikai jellemzők. A keverék ezenkívül nem képes a korróziós folyamatok gátlására, amelyek a fémpolimer alkatrész üzeme és tárolása során a fém ellentest felületén jelentkeznek. ’U.S. Patent No. 704,958 discloses a polyamide-based self-lubricating anti-friction lubricant composition comprising 10-15% by weight lubricating oil, 10-15% by weight polytetra fluoroethylene dry lubricant and 0.5-0.7% ethyleneamine tetraacetic acid. The mixture has high physical-mechanical properties, high abrasion resistance and low friction coefficient. High temperatures (above 100 ° C), however, cause the physical-mechanical properties to deteriorate over time. In addition, the mixture is not capable of inhibiting corrosion processes that occur on the metal counter surface during operation and storage of the metal polymer component. '
A találmány feladata, hogy olyan önkenő súrlódáscsökkentő keveréket dolgozzunk ki, amelyek magas fizikai-mechanikai tulajdonságokkal és kopásállósággal rendelkező alkatrészek előállítását teszi lehetővé, amelyek hosszabb időn keresztül magas hőmérséklétén és agresszív közegben is alkalmazhatók.SUMMARY OF THE INVENTION It is an object of the present invention to provide a self-lubricating anti-friction compound that enables the production of components with high physical-mechanical properties and abrasion resistance, which can be used for extended periods in high temperatures and in aggressive media.
A találmány tárgya tehát önkenő súrlódáscsökkentő készítmény, amely pollamidot, kenőolajat és száraz kenőanyagot tartalmaz. A találmány szerinti készítmény jellemző vonása, hogy poliamidként polikaproamidot, önthető poliamidot vagy üvegszállal erősített poliamidot, kenőolajként 0,85—10 g/cm3 sűrűségű ásványi olajat vagy 0,9-1,3 g/cm3 sűrűségű szilikon olajat száraz kenőanyagként grafitot, valamint korróziós inhibitorként — nitrált, parafinnel sűrített ásványolaj rafflnátumot, vagyAccordingly, the present invention relates to a self-lubricating friction reducing composition comprising pollamide, lubricating oil and dry lubricant. The composition aspect of this invention to polyamide polikaproamidot flowable polyamide or glass fiber reinforced polyamide, a lubricating oil 0.85 to 10 g / cm 3 density or mineral oil is from 0.9 to 1.3 g / cm 3 density of silicone oil as a dry lubricant graphite, and, as corrosion inhibitor, nitrated, paraffinic concentrated mineral oil raffinate, or
- dietil-dihexadecil-ammóniumnitrátot vagy- diethyl dihexadecyl ammonium nitrate, or
- etilén-diamin-oleinsav-monoamidot vagy — díciklohexilaminsó és 10—20 szánatomszámú szintetikus zsírsav elegyét vagy- ethylene diamine oleic acid monoamide, or - a mixture of dicyclohexylamine salts and a synthetic fatty acid of 10 to 20 carbon atoms, or
- ciklohexilamin és 7-11 szénatomszámú szintetikus zsírsav sóját vagy — alkenil-butándi-anhidrid és karbamid kondenzációs termékét és poliolefinként nagynyomású polietilént vagy polipropilént tartalmaz, ahol a komponensek aránya noliolefin 5-l5tömeg% kenőolaj 3-l0tömeg% grafit 5-l0tömeg% korróziós Inhibitor l--5tömeg% poliamid 60-86 tömeg%- containing a salt of cyclohexylamine and a C7-C11 synthetic fatty acid, or - a condensation product of alkenyl butanedioic anhydride and urea and polyolefin as a high pressure polyethylene or polypropylene, wherein the proportion of the components is noliolefin 5 to 15% by weight graphite 1-5 wt% polyamide 60-86 wt%
A találmány szerinti önkenő súrlódáscsökkentő készítményt stabil fizikai-mechanikai és súrlódáscsökkentő tulajdonsággal rendelkezik magas hőmérsékleten is (150 °C-ig), csökkenti a folyamatos vagy szakaszos üzemmódban dolgozó súrlódó alkatrészek hasadási korrózióját és konzerváló hatása segítségével csökkenti az összekapcsolt fémalkatrészek mechanikai kopásának intenzitását.The self-lubricating friction reducing composition of the present invention exhibits stable physical-mechanical and friction-reducing properties at high temperatures (up to 150 ° C), reduces frictional corrosion of friction components in continuous or batch mode, and reduces its mechanical wear intensity through its preservative effect.
A találmány szerinti készítményben a poliolefln biztosítja az önkenő hatást nagy sebességeknél és magas igénybevételnél (magas hőmérséklet). A kenőolaj biztosija az önkenő hatást alacsony hőmérsékleteknél (legfeljebb 80-100 °C). A grafit biztosítja az alacsony súrlódási együtthatót és növeli a keverék kopásállóságát.In the composition of the invention, the polyolefin provides a self-lubricating effect at high speeds and high stress (high temperature). The lubricating oil provides a self-lubricating effect at low temperatures (up to 80-100 ° C). Graphite provides a low coefficient of friction and increases the abrasion resistance of the blend.
Olajban oldódó korróziós inhibitor alkalmazása csökkenti az összekapcsolt fémalkatrészek agresszív közegben (elektrolitok, savas és lúgok vizes oldata) történő alkalmazás esetén fellépő korróziós folyamatok intenzitását. Az alkalmazott korróziós inhibitor ezenkívül antloxldáns hatást fejt ki a keverék polimer alapját képező poliamiddal szemben, ami lehetővé teszi, hogy egy komponens segítségével egyidejűleg csökkentsük a polimer keverék hőbomlását, valamint korróziós folyamatokat, amelyek a polimer keverék és a fémalkatrész határán lépnek fel.,The use of an oil-soluble corrosion inhibitor reduces the intensity of the corrosion processes of the metal components bonded together when used in aggressive media (electrolytes, acidic and alkaline aqueous solutions). The corrosion inhibitor used also exhibits an anthloxantant effect on the polymer-based polyamide of the blend, which allows the use of a component to simultaneously reduce the thermal decomposition of the polymer blend and corrosion processes that occur at the boundary between the polymer blend and the metal part.
A poliolefln és a folyékony fázisú komponens (kenőolaj + korróziós inhibitor) tömegaránya ΙΌ,8-1:1. Ezt az arányt az alábbi meggondolások határozzák meg. Ismert, hogy ha poliolefint folyékony fázisú plasztiflkátorral töltünk meg (40-50 tömeg%), majd a keveréket megolvasztjuk, kolloid oldat keletkezik, amely lehűlés közben géllé, vagyis befejezetlen fázisszétválást mutató rendszerré alakul. A keletkező polimerváz egymással kapcsolatban lévő sejteket (pórus) tartalmaz, amelynek mérete 10—30 μιη, amelyekben folyadék (polisztifikátor) található. Színerézissel biztosíthatjuk a folyadék egyenletes eloszlását a gél pórusaiban. A találmány szerinti készítményben a kenő-21 olajból és olajban oldódó korróziós inhibitorból álló folyadék fázis a poliolefin plasztifikátoraként működik. A polimer gél egyenletesen oszlik el a találmány szerinti keverék térfogatában, és ennek következtében az említett folyékony fázisú komponens egyenletesen válik ki a találmány szerinti keverékből előállított termék felületén. A fém ellentest által kiváltott súrlódás hatására a folyékony fázisú komponens elhasználódik, ennek ütemében azonban megismétlődik az inhibitort tartalmazó kenőolajnak az alkatrész belsejéből a súrlódási felületre történő transzportja. Ez biztosítja a keverék súrlódáscsökkentő és korróziós viselkedésének önszabályozását.The weight ratio of polyolefin to liquid phase component (lubricating oil + corrosion inhibitor) is ΙΌ, 8-1: 1. This ratio is determined by the considerations below. It is known that when a polyolefin is filled with a liquid phase plasticizer (40-50% by weight) and the mixture is thawed, a colloidal solution is formed which, upon cooling, becomes a gel, i.e. an unfinished phase separation system. The resulting polymer backbone contains interconnected cells (pores) of 10-30 µιη in which a liquid (polystyrene) is present. The color distribution can ensure a uniform distribution of the liquid in the pores of the gel. In the composition of the present invention, the liquid phase consisting of lubricating oil 21 and an oil soluble corrosion inhibitor acts as a plasticizer for the polyolefin. The polymer gel is evenly distributed in the volume of the mixture according to the invention, and as a result, said liquid phase component is uniformly deposited on the surface of the product obtained from the mixture according to the invention. The friction caused by the metal counterbody causes the liquid phase component to wear out, but at this rate, the transport of the inhibitor-containing lubricating oil from the inside of the component to the friction surface is repeated. This provides self-regulation of the mixture's anti-friction and corrosion behavior.
Ha a keverék poliolefin tartalma 5 törne g% alá csökken, romlanak az önkenő tulajdonságok. Ezzel szemben a 11 tömeg%-nál több poliolefin tartalom rontja a fizikai-mechanikai jellemzőket. Ugyanilyen hatások határozzák meg a folyékony komponens (kenőolaj + korróziós inhibitor) mennyiségét. Mint már említettük, a folyékony fázisú kötőanyag bizonyos arányban áll a poliolefinnel. Egy tömeg%-nál kevesebb mennyiségű korróziós inhibitor esetén romlik a keverék korróziós viselkedése, míg egy tönieg%-nál több inhibitor alkalmazása felesleges, mivel nem jár a korróziós tulajdonságok javulásával.If the polyolefin content of the blend falls below 5% by weight, the self-lubricating properties deteriorate. In contrast, more than 11% by weight polyolefin content impairs physical-mechanical properties. The same effects determine the amount of liquid component (lubricating oil + corrosion inhibitor). As mentioned above, the liquid phase binder has a certain proportion to the polyolefin. With less than 1% by weight of corrosion inhibitor, the corrosion behavior of the mixture deteriorates, while using more than 1% by weight of the inhibitor is unnecessary as it does not improve the corrosion properties.
tömeg%-nál kevesebb grafit alkalmazása csökkenti a keverék súrlódáscsökkentő hatását (ami növeli a súrlódási együtthatót és a kopást), míg 10 tömeg%-nál több grafit csökkenti a fizikai-mechanikai tulajdonságokat.Use of less than 10% by weight of graphite reduces the friction reducing effect of the mixture (which increases the coefficient of friction and wear), and more than 10% by weight of graphite reduces the physical-mechanical properties.
A találmány szerinti önkenő súrlódáscsökkentő készítmény előállításához a poliamid granulátumot 100-110 °C hőmérsékleten mennyisége nem lépheti túl a 0,1 -0,15 tömeg%-ot), majd a poliolefin-granulátumot és a grafitport hozzáadjuk és a keveréket óvatosan elkeverjük. Ezután hozzáadjuk a kenőolajat, amelyben előzőleg feloldottuk a korróziós inhibitort. A kapott keveréket tetszőleges típusú keverőberendezésben, például dobmalomban homogén összetétel eléréséig keverjük. A keveréket nagyteljesítményű szalagsajtoló eljárással vagy 220-270 °C hőmérsékleten végrehajtott öntéssel (a poliamid típusától függően) kívánt termékké dolgozzuk fel.In order to prepare the self-lubricating friction reducing composition of the present invention, the amount of polyamide granulate at 100-110 ° C should not exceed 0.1-0.15% by weight), then the polyolefin granulate and the graphite powder are added and the mixture is mixed gently. The lubricating oil in which the corrosion inhibitor has previously been dissolved is then added. The resulting mixture is blended in any type of mixer such as a drum mill until a homogeneous composition is obtained. The mixture is processed by a high-performance belt extrusion process or by casting at 220-270 ° C (depending on the type of polyamide) to the desired product.
Ha a termék felhasználási területek következtében nincs szükség arra, hogy a folyékony fázisú komponenst a termék teljes térfogatából a felületre transzformáljuk, úgy a termék előállítása során eljárhatunk úgy is, hogy a szilárd fázisú komponensekből (poliamid, poliolefin és grafit keveréke) a kívánt munkadarabot például öntési eljárással formáljuk, majd egy tartóba helyezzük, amelyet folyékony fázisú komponensekkel töltöttünk meg, ahol a folyékony fázis kenőolaj és olajban oldódó korróziós inhibitor 2:1-3:1 tömegarányú keverékéből áll. A folyadékfázis hőmérséklete a poliolefin olvadáspontja felett legyen, de 80-90%-nál jobban ne közelítse meg a keverék alapját képező poliamid olvadáspontját. A tartózkodási idő az inhibitort tartalmazó kenőolaj behatolásának kívánt mélységétől függ. Az átitatás sebessége 500 pm mélységig 8-10 gm/perc. Az átitatás után a termék felületi rétegének összetétele azonos a találmány szerinti készítmény összetételével. ’If, due to the application of the product, it is not necessary to transform the liquid phase component from the total volume of the product to the surface, the product may be manufactured by preparing the desired workpiece from the solid phase components (polyamide, polyolefin and graphite) The liquid phase consists of a 2: 1 to 3: 1 by weight mixture of a lubricating oil and an oil soluble corrosion inhibitor. The temperature of the liquid phase should be above the melting point of the polyolefin, but should not be closer to 80-90% of the melting point of the polyamide on which the mixture is based. The residence time depends on the desired depth of penetration of the lubricating oil containing the inhibitor. The impregnation rate is 500 to 10 µm / min up to 500 µm. After impregnation, the composition of the surface layer of the product is the same as that of the composition of the invention. '
A találmány szerinti készítményben poliamidként a következők használhatók:The following polyamides can be used in the composition according to the invention:
- pollakroamid (önthető gyanta), e-kaprolaktám katalizátor jelenlétében végrehajtott hidrolitikus polimerizációjának terméke, granulátum, 1—5 mm átmérővel, sűrűsége: 1130 kg/m3, olvadáspont 215 °C,húzási szilárdság 55-77 MPa, nyomószilárság 100-150 MPa, móltömeg 1000-3500, — önthető poliamid, hexametilén-diamin-só és szebadnsav polikondenzádós terméke, 3—55 mm átmérőjű granulátum, sűrűség: 1140 kg/m3, olvadáspont 252-260 °C, húzási szilárdság 80 MPa, móltömeg 2000, — üvegszállal erősített poliamid, polikaproamid-gyanta, amely 9-11 pm átmérőjű üvegszálakat tartalmaz 30 tömeg% mennyiségben 3-9 mm átmérőjű granulátum, sűrűség: 1360 kg/m3, olvadáspont: 217 °C, húzószilárdság: 115 MPa, nyomószilárdság: 180 MPa, móltömeg 10000—3500.- Pollacroamide (pourable resin), product of hydrolytic polymerization in the presence of e-caprolactam catalyst, granules, 1-5 mm in diameter, density: 1130 kg / m 3 , melting point 215 ° C, tensile strength 55-77 MPa, compressive strength 100-150 MPa , polycondensed product of pourable polyamide, hexamethylenediamine salt and sebadic acid, granules having a diameter of 3 to 55 mm, density: 1140 kg / m 3 , melting point 252-260 ° C, tensile strength 80 MPa, molecular weight 2000, - glass fiber reinforced polyamide, polycaproamide resin, containing 30% by weight of glass fibers 9 to 11 µm in diameter, granules having a diameter of 3 to 9 mm, density: 1360 kg / m 3 , melting point: 217 ° C, tensile strength: 115 MPa, compressive strength: 180 MPa, molecular weight 10000-3500.
Poliolefinként előnyösen alkalmazható a nagynyomású polietilén (sűrűség: 900—939 kg/m3), valamint polipropilén (sűrűség: 900-910 kg/m3).Preferred polyolefins are high pressure polyethylene (density: 900-939 kg / m 3 ) and polypropylene (density: 900-910 kg / m 3 ).
Kenőanyagként például ásványi olajokat alkalmazunk:Examples of lubricants are mineral oils:
a) ötvözetlen ásványolaj rafinátum, édesjiaraffinos és paraffinszegény kőolajból, sűrűség 20 dC hőmérsékleten 0,89 g/cm3, viszkozitás: 20 °C hőmérsékleten 1,4 x IO'5 m2/s hamutartalom legfeljebb 0,003%, savszám 0,25 mg KOH/g, dermedéspont: -30 °C, lobbanáspont zárt tégelyben: 200 °C,a) the alloy petroleum raffinate, and édesjiaraffinos paraffinszegény petroleum oil, density at 20 C, d 0.89 g / cm 3, viscosity at 20 ° C, 1.4 x IO "5 m 2 / s ash content is up to 0.003%, acid number 0.25 mg KOH / g, freezing point: -30 ° C, flash point: 200 ° C,
b) ötvözetlen ásványolaj rafinátum, kénszegény kőolaj fajtákból sűrűség: 20 °C hőmérsékleten 0,987 g/cm , viszkozitás: 20 °C hőmérsékleten 2,05 x 10'5 m2/s, hamutartalom: legfeljebb 0,003%, savszám: 0,03 mg KOH/g, dermedéspont: 018 fc, lobbanáspont zárt tégelyben: 250 °C,(b) Unrefined petroleum refined coal, of low sulfur petroleum species, density at 20 ° C: 0,987 g / cm, viscosity at 20 ° C: 2,05 x 10 5 m 2 / s, ash content: not more than 0,003%, acid value: 0,03 mg KOH / g, pour point: 018 fc, flash point: 250 ° C,
c) tiszta ásványolaj, sűrűség: 20 °C hőmérsékleten 0,894 a/cm3, viszkozitás: 20 v hőmérsékleten 4,9 x x 10'y m’/s 50 °C hőmérsékleten 2,0 x 10'5 m2/s dermedéspont: 045 °C, lobbanáspont nyitott tégelyben: 163 bC.c) Pure mineral oil, density: 0.894 a / cm 3 at 20 ° C, viscosity: 20 v 4.9 xx 10 ' y m' / s at 50 ° C 2.0 x 10 ' 5 m 2 / s freezing point: 045 ° C, flash point in open jar: 163 b C.
Kenőolajként felhasználhatók még szilikonolajok (folyékony, szerves szilíciumvegyületek), valamint kis móltömegű szerves sziloxán poúmerek, amelyek széles hőmérséklethatáron belül képesek egy folyadék tulajdonságait megtartani, kémiailag inertek, korrózióállóak, aromás és klórozott alifás szénhidrogénekben oldódnak, és kőolajbázisú kenőolajokkal összeférhetők. A szilikonolajok közül példaként említhetők a következők:Other lubricating oils are silicone oils (liquid organic silicon compounds) and low molecular weight organic siloxane polymers which are capable of maintaining the properties of a liquid over a wide range of temperatures, chemically inert, corrosive, soluble in aromatic and chlorinated aliphatic hydrocarbons and. Examples of silicone oils include:
d) poHetil-sziloxán folyadék, sűrűség: 20 °C hőmérsékleten 0,97 g/cm3, viszkozitás: 20 °C hőmérsékleten 4,2 x 10 5 m2s forráspont: 250 °C, lobbanáspont nyitott tégelyben: 170 °C, spedfikus hőkapacitás: 20 °C hőmérsékleten 1,863 x 103 J/kg.fok,d) Polyethylsiloxane liquid, density: 0.97 g / cm 3 at 20 ° C, 4.2 x 10 5 m 2 at 20 ° C, boiling point: 250 ° C, flash point: 170 ° C, specific heat capacity: 1,863 x 10 3 J / kg degree at 20 ° C,
e) polimetil-sziloxán folyadék, sűrűség: 20 °C hőmérsékleten 1,08 g/cm3, viszkozitás: 20 °C hőmérsékleten 2,0 χθΙΟ5 m2/s dermedéspont: -60 °C, forráspont: 250 °C, lobbanáspont nyitott tégelyben: 265e) Polymethylsiloxane liquid, density: 1.08 g / cm 3 at 20 ° C, viscosity: 2.0 χθΙΟ 5 m 2 / s at 20 ° C freezing point: -60 ° C, boiling point: 250 ° C, flash point in open jar: 265
C, spedfikus hőkapadtás: 20 °C hőmérsékleten 1,641 x 103 J/kgfok,C, spedical heat capture: 1,641 x 10 3 J / kg at 20 ° C,
f) polimetil-fenikziloxán folyadék, sűrűség: 20 eC hőmérsékleten 1,18 g/cm3, viszkozitás: 20 °Chőmérsékleten 5,4 x IO'5 m2/s dermedéspont: 036 °C, forráspont: 360 °C, spedfikus hőkapadtás: 20 °C hőmérsékleten 1,423 x 103 J/kg.fok.f) polymethyl fenikziloxán liquid density at 20 C E 1.18 g / cm 3, viscosity: 5.4 x 20 ° Chőmérsékleten IO '5 m 2 / s, pour point: 036 ° C, boiling point: 360 ° C, spedfikus heat capture: 1.423 x 10 3 J / kg at 20 ° C.
. A találmány szerinti készítményekben olajba oldódó korróziós inhibitorként hatásosan alkalmazhatók az -NO2, = 0 csoportokat tartalmazó donor típusú inhibitorok, és az -NH2, -OH csoportokat tartalma-31. Oil-soluble corrosion inhibitors useful in the compositions of the present invention include donor-type inhibitors having -NO 2 , = O groups and containing -NH 2 , -OH groups.
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Zó akceptor típusú Inhibitorok.Zon acceptor type Inhibitors.
Donor típusú korróziós inhibitorokra példaként említhetők:Examples of donor-type corrosion inhibitors include:
A) nitrált, paraffinnal (10 tömeg%) sűrített ásványolaj raffinátum, olajszerű folyadék, sötétbarna szín sűrűség: 0 96 g/cm3 (20 °C), viszkozitás: 1,00 x 10'4 m2/s (20 °C) és 3,0 x 10‘5 m2/s (100 °C), hamutartalom: 3,5%, ásványi olajokban és szerves oldószerekben oldódik, -NO2 csoportot tartalmaz,A) Nitrated paraffin (10 wt.%) Concentrated mineral oil raffinate, oily liquid, dark brown color density: 0 96 g / cm 3 (20 ° C), viscosity: 1.00 x 10 4 m 2 / s (20 ° C) ) and 3.0 x 10 5 m 2 / s (100 ° C), ash content: 3.5%, soluble in mineral oils and organic solvents, contains -NO 2 ,
B) [(C2H5)2 N (C14H33)] NO2 képletű dietil-dihexadecil-ammóniumnitrát,B) [(C 2 H 5 ) 2 N (C 14 H 33 )] NO 2 diethyl dihexadecyl ammonium nitrate,
C) NH2CH2CH2NHCO-C)7H33 képletű etilén-diamin-oleinsav-monoamld.C) NH 2 CH 2 CH 2 NHCO-C) 7 H-oleic acid-ethylenediamine monoamld formula 33rd
Akceptor típusú korróziós inhibitorként előnyösen alkalmazhatók a következők:Preferred acceptor type corrosion inhibitors include:
D) dlciklohexilaminsó (43 tömeg%) és 10-20 szénatomos szintetikus zsírsav (57 tömeg%) (C*Hu)2'NHC Hn^jCOOH általános képletű elegye, pasztaszeru termek, sűrűség: 0,92 g/cnr (20 °C), olvadáspont: 15—20 °C, olajban és szerves oldószerekben oldódik,D) Mixture of dlcyclohexylamine salt (43% w / w) and C 10-20 synthetic fatty acid (57% w / w) (C * Hu) 2 'NHC Hn 1 / COOH, paste, density: 0.92 g / cnr (20 ° C) ), melting point: 15-20 ° C, soluble in oil and in organic solvents,
E) ciklohexllamin és 7-11 szénatomszámú szintetikus zsírsav sója, (CnH2p+jCOOHC#H, ,NH2 általános képlet), pasztaszeru termék, sötétbarna szín, dermedéspont -12 °C, alkoholban, olajba, benzinben és acetonban oldódik, sűrűség 0,92 g/cm3,E) Salt of Cyclohexyllamine and C 7-11 Synthetic Fatty Acid (Formula C n H2 p + jCOOHC # H, NH 2 ), paste product, dark brown color, melting point -12 ° C, soluble in alcohol, oil, gasoline and acetone 0.92 g / cm 3 ,
F) alkenil-butándi-anhidrid és karbamid kondenzációs terméke, világosbarna folyadék, sűrűség: 0,89 g/cm3 (20 °C), viszkozitás: 2,5 x 10-5 m2/s (50 °C), olajban és szerves oldódik, -NH2 csoportot tartalmaz.F) a condensation product of an alkenyl-butanediyl anhydride and urea, light brown liquid, density: 0.89 g / cm 3 (20 ° C), viscosity: 2.5 x 10- 5 m 2 / s (50 ° C) oil and organic soluble, containing -NH 2 .
Az Inhibitorok hatásmechanizmusa a következő: A súrlódási felületre érve a donor típusú inhibitorok felesleges elektronokat a fém ellentestnek leadják és annak felületén kemoszorpciós vegyületet képeznek.The mechanism of action of Inhibitors is as follows: Upon reaching the friction surface, donor-type inhibitors release excess electrons into the metal counterpart and form a chemosorption compound on the surface.
’υ Az akceptor típusú inhibitorok felfogják a fém elektronjait és kemoszorpciós réteget képeznek, amely a fém ellentest felületét védi a korróziótól. A kiválasztott Inhibitor típusok ezenkívül antioxidációs szert, valamint olyan anyagokat tartalmaznak, amelyek gá1 g tolják a polimerek hőoxidációs roncsolását. Az donor típusú korróziós inhibitorok antioxidáns szert és redukálószert tartalmaznak, például szerves szulfidokat, szelenldeket, vagy zsíraromás fcszfltokat, amelyek a poliamid hiperoxid csoportjával szabad csoportok képződése nélkül reagálnak. Az akceptor inhibitorok aromás amidokat és alkilezett fenolokat tartalmaznak, amelyek blokkolják a poliamid oxidációját, vagyis a szabad aktív csoportokkal reagálnak. 'Υ The acceptor-type inhibitors absorb electrons and form metal kemoszorpciós layer which protects the metal against the body surface from corrosion. The selected Inhibitor types also contain an antioxidant as well as substances that inhibit the thermal oxidation degradation of the polymers. The donor-type corrosion inhibitors contain an antioxidant agent and a reducing agent, such as organic sulfides, selenides, or fatty aromatic fatty acids, which react with the hyperoxide group of the polyamide without forming free groups. Acceptor inhibitors contain aromatic amides and alkylated phenols which block the oxidation of the polyamide, i.e., react with free active groups.
Néhány találmány szerinti összetételt, valamint a 704 958, számú szovjet szerzői tanúsítványban ismertetett készítmény összetételét az 1. táblázat mutatja.Some of the compositions of the invention as well as the composition of the composition disclosed in US Patent No. 704,958 are shown in Table 1.
1. táblázatTable 1
198.519198 519
A 2, táblázat az 1. táblázatban szereplő összetételek fizikai-mechanikai tulajdonságait (húzószilárdság és nyomószilárdság), súrlódási tulajdonságait (súrlódási együttható és kopáslntenzltás), valamint korróziós viselkedését mutatják.Table 2 shows the physical-mechanical properties (tensile strength and compressive strength), frictional properties (friction coefficient and abrasion resistance), and corrosion behavior of the compositions in Table 1.
A találmány szerinti önkenő súrlódáscsökkentő keverék fizikai-mechanikai tulajdonságait szakítógép segítségével állapítottuk meg 50 mm/perc sebesség mellett.The physical-mechanical properties of the self-lubricating anti-friction mixture of the present invention were determined using a tensile machine at 50 mm / min.
A súrlódási vizsgálatokat tengely-betét sémával dörzsgépen végeztük. Ellentestként szénacélt alkalmaztunk, amely 0,42—0,50 tömeg% szenet tartalmaz, HRC keménysége: 40-45, durvasága (R ) = 0,8—1 jum. Az önkenő súrlódáscsökkentő készítményből előállított munkadarab felülete 2 cm1. A lineáris sebesség 0,1-1,0 m/sec, terhelés: 2,5, illetve 0,5 PMa. A kopásintenzitás (I) az alábbi képlet alapján számolható ki;Friction tests were performed on a shaft-insert scheme on a friction machine. Carbon steel containing 0.42-0.50% carbon by weight, HRC hardness 40-45, and coarseness (R) = 0.8-1 µm was used as the counterpart. The workpiece made of the self-lubricating anti-friction composition has a surface of 2 cm 1 . The linear velocity is 0.1-1.0 m / sec and the load is 2.5 and 0.5 PMa, respectively. The wear intensity (I) can be calculated using the formula below;
AGBRANCH
J,------JO-·,J · ------ Jo,
p.A.S a képletbenp.A.S in the formula
ÁG = tömegre vonatkoztatott kopás, mg, δ = a mintadarab sűrűsége 20 °C hőmérsékleten, g/cm3,ÁG = mass weight wear, mg, δ = density of the sample at 20 ° C, g / cm 3 ,
A =a munkadarab felülete, cm1,A = workpiece surface, cm 1 ,
S = súrlódási út, km. ’S = friction distance, km. '
A korróziós vizsgálatokat gyorsított eljárással végeztük, amelynek során elektrolitba merített és a vizsgálandó anyagból készített mintadarabbal kapcsolódó két elektróda polarizációs ellenállását (Rp) mértük. Ehhez 0,09-15 tömeg% szenet tartalmazó szénacél•jq ból készült elektródákat alkalmaztuk. A hatásos elektróda fel ületet Ra = 0,4-0,5 μπι durvaságig csiszoltuk, és az üzemen kívüli felületet paraffinnal szigeteltük. Elektrolitként 0,ln HCl oldatot és In NajSO4 oldatot alkalmaztunk.Corrosion tests were carried out by an accelerated method, which measured the polarization resistance (Rp) of two electrodes immersed in an electrolyte and connected to a sample of the material to be tested. Electrodes made of carbon steel containing 0.09 to 15% by weight of carbon were used. The effective electrode tip overlay was polished to a roughness R a = 0.4-0.5 μπι and the inactive surface was sealed with paraffin. The electrolyte used was 0.1 l HCl and In NajSO 4 .
A korrózió sebességét (, g/m1 óra) az alábbi kép15 lettelszámoltuk:The corrosion rate (, g / m 1 h) was calculated as follows:
2K2K
I»------,I »------,
S.Rp a képletbenS.Rp in the formula
K = korrózió tömegegyütthatója, amely az elektrolit fajtájától és koncentrációjától függ, ohm g/óra (0,ln HG oldatban K = 20,1, In NajSO* oldatban K = “0,032),K = weighting factor of corrosion, depending on the type and concentration of the electrolyte, ohm g / h (0, ln in HG solution K = 20,1, in In NajSO * solution K = '0,032),
Rp - polarizációs ellenállás, ohm, λ- S = elektródafelület, m1.Rp - polarization resistance, ohm, λ- S = electrode surface, m 1 .
(Zaschita Metallov, 6. szám. Verlag Nauka, Moszkva, 1982.946-949. oldal)(Zaschita Metallov, No. 6, Verlag Nauka, Moscow, 1982, pp. 946-949)
198.519 b-b1 °sss198,519 b-b1 ° sss
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A 2. táblázat eredményeiből látható, hogy a korróziós Ihhibitor jelentős mértékben növeli a találmány szerinti készítményből előállított munkadarabok hőjtabilitását, vagy a hőoxidációval szemben ellenállást, így a húzószilárdság 150 °C hőmérsékleten 100 órán keresztül végzett höoxidálás után a találmány szerinti keveréknél mindössze 5- 20%-kal csökken, míg a 704958. számú szovjet szerzői tanúsítvány szerinti készítménynél a húzószilárdság kevesebb, mint felére csökken. Korróziós inhibitorok alkalmazásával a szénalkatrész korróziójának sebességét 50 100-ad részére lehet csökkenteni. Ezzel egyidőben a találmány szerinti készítmény súrlódási tulajdonságai azonosak a 704958. számú szovjet szerzői tanúsítvány szerinti készítmények tulajdonságaival.The results of Table 2 show that the corrosive Ihhibitor significantly increases the thermal stability or the resistance to heat oxidation of the workpieces of the present invention, so that after tensile oxidation at 150 ° C for 100 hours, the tensile strength of the composition according to the invention is only 5-20%. , while the tensile strength is less than half that of the composition according to Soviet Authorization No. 704958. By using corrosion inhibitors, the rate of corrosion of the carbon moiety can be reduced by 50 to 100. At the same time, the frictional properties of the composition according to the invention are the same as those of the composition according to the US Patent No. 704958.
A találmány szerinti készítményből előállított termékeket súrlódó alkatrészként alkalmaztuk gépjárműveknél, mezőgazdasági gépeknél, kőolaj- és gázberendezéseknél. A vizsgálatok eredményei alapján a találmány szerinti készítményből előállított alkatrészek lényegesen jobban alkalmazhatók, mint a súrlódásellenes öntöttvas, a babbit, valamint a réz, alumínium és cink tartalmú ötvözetek.The products of the present invention have been used as friction components in motor vehicles, agricultural machinery, and oil and gas installations. According to the results of the tests, the components of the composition according to the invention are significantly better used than anti-friction cast iron, babbit and alloys containing copper, aluminum and zinc.
A találmány szerinti önkenő súrlódáscsökkenő készítmény magas fizikai-mechanikai és súrlódáscsökkentő tulajdonságokkal rendelkezik, és lehetővé teszi a súrlódó alkatrészek hasadási korróziójának gátlását és ezáltal az alkatrészek mechanikai korróziós kopásának csökkentését. Stabilizálják az alkatrészek fizikai-mechanikai tulajdonságait magas hőmérsékleten és technológiailag könnyen feldolgozhatok.The self-lubricating anti-friction composition of the present invention has high physico-mechanical and anti-friction properties and allows the inhibition of frictional corrosion of frictional components and thereby the reduction of mechanical corrosion wear of the components. They stabilize the physical-mechanical properties of components at high temperatures and are easy to process technologically.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/SU1985/000043 WO1986007074A1 (en) | 1985-05-23 | 1985-05-23 | Self-lubricating antifriction composition |
Publications (2)
Publication Number | Publication Date |
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HUT43332A HUT43332A (en) | 1987-10-28 |
HU198519B true HU198519B (en) | 1989-10-30 |
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HU853699A HU198519B (en) | 1985-05-23 | 1985-05-23 | Self-lubricating anti-friction mixture |
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CH (1) | CH668774A5 (en) |
DE (1) | DE3600021A1 (en) |
DK (1) | DK31587A (en) |
FI (1) | FI870271A (en) |
FR (1) | FR2592654B1 (en) |
GB (1) | GB2186882B (en) |
HU (1) | HU198519B (en) |
NL (1) | NL8520248A (en) |
SE (1) | SE462654B (en) |
WO (1) | WO1986007074A1 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
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US4915856A (en) * | 1987-07-10 | 1990-04-10 | Durafilm Corporation | Solid lubricant composition |
GB2207146B (en) * | 1987-07-10 | 1991-07-24 | Durafilm Materials Corp | Solid lubricant composition |
US5227080A (en) * | 1990-10-10 | 1993-07-13 | Integral Corporation | Intrinsically lubricated material compositions and products thereof |
WO1995013341A1 (en) * | 1993-11-12 | 1995-05-18 | Aktsionernoe Obschestvo Zakrytogo Tipa 'amtek' | Anti-friction modifying compound |
CN114606041B (en) * | 2022-03-16 | 2023-01-24 | 四川大学 | Wear-resistant lubricant based on modified halloysite and preparation method thereof |
Family Cites Families (7)
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DE2526194A1 (en) * | 1974-06-12 | 1976-01-02 | Asahi Chemical Ind | Thermoplastic moulding materials with high lubricity - contg base resin, lubricating oil, high density polyethylene and filler |
US4001124A (en) * | 1975-03-17 | 1977-01-04 | The Polymer Corporation | Long-wearing plastic bearings |
SU660986A1 (en) * | 1977-12-13 | 1979-05-05 | Институт Механики Металлополимерных Систем Ан Белорусской Сср | Polymer antifriction self-lubricating composition |
SU704958A1 (en) * | 1978-02-22 | 1979-12-25 | Институт Механики Металлополимерных Систем Ан Белорусской Сср | Antifrictional polymeric founding composition |
DE2849617A1 (en) * | 1978-11-15 | 1980-05-29 | Dow Corning Gmbh | AQUEOUS LUBRICANT |
SU1660986A1 (en) * | 1987-10-28 | 1991-07-07 | Предприятие П/Я Р-6594 | Method for manufacturing articles of polymeric thermal reactive materials |
SU1704958A1 (en) * | 1990-01-23 | 1992-01-15 | Ленинградское конструкторское бюро технологического оснащения | Shell-type face mill |
-
1985
- 1985-05-23 NL NL8520248A patent/NL8520248A/en not_active Application Discontinuation
- 1985-05-23 WO PCT/SU1985/000043 patent/WO1986007074A1/en active Application Filing
- 1985-05-23 HU HU853699A patent/HU198519B/en not_active IP Right Cessation
- 1985-05-23 GB GB8700300A patent/GB2186882B/en not_active Expired
- 1985-12-18 CH CH5389/85A patent/CH668774A5/en not_active IP Right Cessation
-
1986
- 1986-01-02 DE DE19863600021 patent/DE3600021A1/en active Granted
- 1986-01-07 FR FR8600128A patent/FR2592654B1/en not_active Expired
-
1987
- 1987-01-13 SE SE8700097A patent/SE462654B/en not_active IP Right Cessation
- 1987-01-21 DK DK031587A patent/DK31587A/en not_active Application Discontinuation
- 1987-01-22 FI FI870271A patent/FI870271A/en not_active Application Discontinuation
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GB8700300D0 (en) | 1987-02-11 |
FI870271A0 (en) | 1987-01-22 |
DE3600021A1 (en) | 1987-07-09 |
GB2186882A (en) | 1987-08-26 |
SE8700097L (en) | 1987-01-13 |
NL8520248A (en) | 1987-04-01 |
DK31587D0 (en) | 1987-01-21 |
SE8700097D0 (en) | 1987-01-13 |
GB2186882B (en) | 1989-07-12 |
DK31587A (en) | 1987-03-20 |
SE462654B (en) | 1990-08-06 |
FR2592654B1 (en) | 1988-09-16 |
WO1986007074A1 (en) | 1986-12-04 |
FI870271A (en) | 1987-01-22 |
CH668774A5 (en) | 1989-01-31 |
FR2592654A1 (en) | 1987-07-10 |
HUT43332A (en) | 1987-10-28 |
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