US3629103A - Plastic antifriction material - Google Patents
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- US3629103A US3629103A US835785A US3629103DA US3629103A US 3629103 A US3629103 A US 3629103A US 835785 A US835785 A US 835785A US 3629103D A US3629103D A US 3629103DA US 3629103 A US3629103 A US 3629103A
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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
- C10M7/00—Solid or semi-solid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single solid or semi-solid substances
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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
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08L79/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
- C10M2201/042—Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/05—Metals; Alloys
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/06—Metal compounds
- C10M2201/065—Sulfides; Selenides; Tellurides
- C10M2201/066—Molybdenum sulfide
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/102—Polyesters
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/024—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/042—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds between the nitrogen-containing monomer and an aldehyde or ketone
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/043—Mannich bases
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/044—Polyamides
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/045—Polyureas; Polyurethanes
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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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
- C10N2040/02—Bearings
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/08—Solids
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Definitions
- Plastic antifriction materials derived from polyimide In order to prepare an aljltifriction "i i noted for its plastics filled with solid lubricants, e.g., graphite or molybenhanced thermal and electrical conduiuvlty metal P denum disulfide are known e.g., powdered copper or silver, are incorporated into the blend of the aforesaid components at the mixing step.
- solid lubricants e.g., graphite or molybenhanced thermal and electrical conduiuvlty metal
- P denum disulfide e.g., powdered copper or silver
- blies such as bearing cages, sliding bearing bushings, and geared transmission components.
- this known antifric- Th 1 tion material exhibits a marked increase of its friction coeffie Y tam mouldmg composition winch consists of a cient with the increase of the working temperatures up to finely dlvlded hpmogeneous powder Subjected to ugh-tem- 70l20f C., whiehprecludes the employment of the material perature mouldmg' under the aforesaid conditions, despite its good mechanical above PmFedure ylelds an annfncuonmatenal exhlbn' characteristics mg high mechanical strength, good workability, a stable coef- It an object of the present mvenuon to ehmmate the ficlent of friction over awide temperature range, and superior aforementioned disadvantage. wear reslstanc-e' For a better understanding of the present invention, given hereinbelow are the following examples of preparing the antifriction material.
- the resultant polyamidoacid is precipitated mides, exhibit superior performance characteristics due to with a benzene-acetone mixture taken in a five-fold excess and their less pronounced authohesion properties.
- the incorporation of rigid-chain polyarylates or aromatic polyamido acid thus obtained is then polycyclized in vacuo (1 polyamides into a polyimide resin-based antifriction material mm. Hg) at a temperature of 100 C. for 2 hours, at 200 C. exerts a stabilizing effect on the coefficient of friction over a for 3 hours, and at 300 C. for 1.5 hours. wide temperature range.
- Polycyclization yields a polyimide having the following It is expedient to employ an antifriction material of the folstructural formula 0 0 II II 0. N O r C O u lowing composition, percent by weight: polyimide, 4-78; filler I (solid lubricants), 2-95, and polyarylates or aromatic polya-
- polyimide, 4-78 polyimide, 4-78; filler I (solid lubricants), 2-95, and polyarylates or aromatic polya-
- the Polylmlde l5 tl'llulated oblaln a homogeneous mides, 1-20. powder.
- solid lubricants 2-75
- polyarylates or aromatic polyamides 1-20
- metal powders 20-40.
- the antifriction material is prepared as follows.
- H H V C C() C -O- be of the following composition, percent by weight: polyimide
- the polyimide obtained in the form of a fused mass is The polyarylate having the aforespecified structure is thoroughly ground to prepare a homogeneous powder which prepared from terephthaloyl chloride and phenolphthalein by is then mixed in a vibrating mill with powdered polyarylate or the high-temperature polycondensation technique.
- the aromatic polyamide and powdered filler solid lubricant, e.g., process is conducted at a temperature of 220 C. for a period molybdenum disulfide or graphite).
- the resultant polyarylate is dissolved in chloroform to obprocessed. tain a 5 percent solution and thereafter precipitated with a
- the polyarylates employed as an antifriction material comfive-fold excess of methyl alcohol, filtered off and dried at a ponent are prepared from aromatic dicarboxylic acid tempe ature of 12 C- for 6 h urs.
- the components are mixed in a vibrating mill to give a equilibrium high-temperature polycondensation method.
- the moulding composition, which is thereafter moulded at a tempolyarylates thus obtained are precipitated with an excess of perature of 390-4 10 C. and a specific pressure of 1,000 to solvent, filtered off and dried to constant weight. 1,200 kg./cm.”.
- EXAMPLE 2 A Polymide of the general formula derived from diphenyl oxide 3,3',4,4'-tetracarboxylic acid dianhydride and m-phenylene diamine, and a polyarylate of the general formula V M I derived from terephthaloyl dichloride and dihydroxydiphenylfluorene are prepared as disclosed in example 1.
- the moulding composition thus prepared is subjected to moulding at a temperature of 490500 C. and a specific pressure of 1.000 to 1,200 kg./cm.
- EXAMPLE 3 Fifty grams of powdered a polyimide prepared as disclosed in example 1 is mixed in a vibrating mill with 420 g. of graphite powder and 20 g. of polymetaphenylene isophthalamide ofthe structural formula Intensity oflinear wear 0.9x 10' Coefficicnt of friction 0.1 Maximum working temperature. C. 250
- EXAMPLE 4 37.5 g. of powdered polyimide prepared as disclosed in example 2 is mixed in a vibrating mill for a period of 2 minutes with 450 g. of graphite powder and 12.5 g. of polyamide havl0 ing the structural formula II 0 h 20 the polyamide being synthesized from anilinephthalein and isophthalic acid by the method disclosed in example 3.
- the moulding powder thus obtained is moulded at a temperature of 490-500 C. and under a specific pressure of 1,000 to 1,200 kg./cm.
- EXAMPLE 5 37.5 g. of powdered polyimide and 12.5 g. of polyarylate prepared as disclosed in example 1, 325 g. of molybdenum disulftde powder (particle size, l-2y.), and 125 g. of copper powder are blended in a vibrating mill for a period of 2 minutes.
- the moulding composition thus obtained is moulded at a temperature of 3904l0 C. and under specific pressure of 1,000 to 1.200 kg./cm.
- EXAMPLE 6 37.5 g. of powdered polyimide prepared as disclosed in example 1. 12.5 g. of polyamide prepared by the procedure of example 3, 325 g. of molybdenum disulfide powder (particle size. 1-2u), and 125 g. of silver powder are mixed in a vibrating mill for a period of 2 minutes.
- the moulding composition thus obtained is subjected to compression moulding at a temperature of 3904l0 C. and under specific pressure of 1,000 to 1,200 kg./cm.
- An antifriction material having a stable coefficient of friction over a wide temperature range comprising 1. 4 to 78 percent by weight of one or more aromatic polyimide resins prepared by polycondensation of an aromatic diamine with an aromatic tetracarboxylic acid dianhydride to yield a polyamido carboxylic acid which after being subjected to polycyclization gives a polyimide,
- rigid-chain polymers selected from the group consisting of a) polyarylates prepared by polycondensation of aromatic dicarboxylic acid chlorides and bisphenols and (b) aromatic polyamides prepared by polycondensation of aromatic diamines and aromatic dicarboxylic acids or their chlorides.
- An antifriction material as in claim 1 which further comprises a powdered metal filler.
- An antifriction material as in claim 2 which comprises 4 to 78 percent of polyimide resin, 2 to 78 percent by weight of solid lubricants, 20 to 40 percent by weight of powdered metal filler, and l to 20 percent by weight of the polyarylate or aro- 6 matic polyamide polymer.
- polyimide is prepared from diphenyl oxide 3,3, 4, 4-tetracarbox' ylic dianhydride and a diamine selected from the group consisting of 4,4-diaminodiphenyl ether and m-phenylenediamine.
- An antifriction material as in claim 1 wherein the polyarylate is prepared from terephthaloyl chloride and a bisphenol selected from the group consisting of phenolphthalein and dihydroxydiphenyl fluorene.
- An antifriction material as in claim 1 wherein the polyamide is prepared from isophthaloyl dichloride and an amine selected from the group consisting of m-phenylenediamine and anilinephthalein.
- An antifriction material as in claim 1 wherein the solid lubricant is selected from the group consisting of molybdenum disulfide and graphite.
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Abstract
A plastic antifriction material containing a polyimide resin, powdered solid lubricants as fillers, and also polyarylates or aromatic polyamides.
Description
United States Patent [72] Inventors Vasily Vladimirovich Korshak ulitsa Gubkina, 4, kv. 81; Irina Alexandrovna Gribova, ulitsa Vavilova, l2, kv. 31; Alexandr Petrovich Krasnov, prospekt Kalinina, 31, kv. 28; Alla Nikolaevna Chumaevskaya, Leninsky prospekt, 101, korpus 163, kv. 86; Olga Svyatoslavovna Natsarenus, ulitsa Grimau, 13, korpus 2, kv. l5; Svellana Vasilievna Vinogradova, Belyaevo-Bogorodskoe, Kvartal 48-a, korpus 6a, kv. 63; Yakov Semenovich Vygodsky, Leninsky prospekt, 101, korpus 135, kv. 38; Vyacheslav Alexandrovich Pankratov, ulitsa Usievicha, 25, kv. 135; Grigory Lvovich Slonimsky, ulitsa Chkalova, l/4, kv. 16, all 01' Moscow, U.S.S.R.
[21] Appl. No. 835,785
[22] Filed June 23, 1969 [45] Patented Dec. 21, 1971 [54] PLASTIC ANTlFRlCTlON MATERIAL 8 Claims, No Drawings [52] U.S.Cl 252/12 [51] lm. Cl C10m 7/34 [50] Field of Search 252/12, 12.2, 12.4, 12.6
[56] References Cited UNITED STATES PATENTS 2,698,966 1/1955 Stott et al. 252/12 3,122,505 2/1964 Rulon-Miller et al 252/12 3,287,288 11/1966 Reiling 252/12 Primary Examiner--Daniel E. Wyman Assistant Examiner-l. Vaughn Attorney-Waters, Roditi, Schwartz & Nissen ABSTRACT: A plastic antifriction material containing a polyimide resin, powdered solid lubricants as fillers, and also polyarylates or aromatic polyam ides.
PLASTIC ANTIFRlCTlO N MATERIAL V 4 To preparethe aromatic polyamides used as an antifriction This invention relates to plastic antifriction materials inmaterlal f i afomanc dmmlnes and aromatic dwarf tended for the fabrication of elements of dry-friction assemboxyhc acld chlorides m a etrahydmfuran'wateSoda medlum are subjected to low-temperature olycondensation, fol- 5 lowed by filtering off and drying the resultant polymers.
Plastic antifriction materials derived from polyimide In order to prepare an aljltifriction "i i noted for its plastics filled with solid lubricants, e.g., graphite or molybenhanced thermal and electrical conduiuvlty metal P denum disulfide are known e.g., powdered copper or silver, are incorporated into the blend of the aforesaid components at the mixing step.
blies, such as bearing cages, sliding bearing bushings, and geared transmission components.
When used in dry friction assemblies, this known antifric- Th 1 tion material exhibits a marked increase of its friction coeffie Y tam mouldmg composition winch consists of a cient with the increase of the working temperatures up to finely dlvlded hpmogeneous powder Subjected to ugh-tem- 70l20f C., whiehprecludes the employment of the material perature mouldmg' under the aforesaid conditions, despite its good mechanical above PmFedure ylelds an annfncuonmatenal exhlbn' characteristics mg high mechanical strength, good workability, a stable coef- It an object of the present mvenuon to ehmmate the ficlent of friction over awide temperature range, and superior aforementioned disadvantage. wear reslstanc-e' For a better understanding of the present invention, given hereinbelow are the following examples of preparing the antifriction material.
It is a further and more specific object of the present invention to provide an antifriction material noted for its stable coefficient of friction over'a wide temperature range.
' This object is accomplished by the provision of a plastic an- EXAMPLE 1 tlfriction material derived from a polyimide resin filled with powdered solid lubricants and also containing, according to Dianhydride f diphenyl oxide-3.3. .4-tetracarboxylic the invention, polyarylates or aromatic polyamides. acid and diaminodiphenyl ether taken in a molar ratio of 1:1 Under dry friction conditions when polymer molecules are are subjected to polycondensation in dimethylformamide at a subjected to both thermal effects and mechanical cracking, temperature of 10-25 C. for a period of 4 hours, with conrigid-chain polymers, such as polyarylates or aromatic polyatinuous stirring. The resultant polyamidoacid is precipitated mides, exhibit superior performance characteristics due to with a benzene-acetone mixture taken in a five-fold excess and their less pronounced authohesion properties. dried in a vacuum cabinet at 80 C. for 2 hours. The dry The incorporation of rigid-chain polyarylates or aromatic polyamido acid thus obtained is then polycyclized in vacuo (1 polyamides into a polyimide resin-based antifriction material mm. Hg) at a temperature of 100 C. for 2 hours, at 200 C. exerts a stabilizing effect on the coefficient of friction over a for 3 hours, and at 300 C. for 1.5 hours. wide temperature range. Polycyclization yields a polyimide having the following It is expedient to employ an antifriction material of the folstructural formula 0 0 II II 0. N O r C O u lowing composition, percent by weight: polyimide, 4-78; filler I (solid lubricants), 2-95, and polyarylates or aromatic polya- The Polylmlde l5 tl'llulated oblaln a homogeneous mides, 1-20. powder.
in order to enhance the thermal and electrical conductivity 8- of the Powdered Polylmlde, 450 of Powdered of the present antifriction material, to improve its moldability molybdenum dlsulfide (parlklle Size and 8- of and also to raise its hardness and wear resistance, it is good p l f l' p y y ofthe following Structural formula practice to additionally incorporate thereinto metal powders as fillers.
-78; solid lubricants, 2-75; polyarylates or aromatic polyamides, 1-20, and metal powders, 20-40.
The antifriction material, according to the present invention, is prepared as follows.
Polycondensation of an aromatic diamine with an aromatic O tetracarboxylic acid dianhydride yields a polyamido carboxyli id, hi h, on b i ubj t d t olycyclization gives a are mixed in a vibrating mill for 2 minutes until a homogeneo v 0 7 1n the latter case, the antifriction material should preferably H H V C C() C -O- be of the following composition, percent by weight: polyimide,
polyimide. ous mass is obtained.
The polyimide obtained in the form of a fused mass is The polyarylate having the aforespecified structure is thoroughly ground to prepare a homogeneous powder which prepared from terephthaloyl chloride and phenolphthalein by is then mixed in a vibrating mill with powdered polyarylate or the high-temperature polycondensation technique. The aromatic polyamide and powdered filler (solid lubricant, e.g., process is conducted at a temperature of 220 C. for a period molybdenum disulfide or graphite). The polyarylate o amof 12 hours and comprises stirring, in a stream of argon, a mix matic polyamide used as a component of the antifriction ture of equimolar amounts of the starting compounds dismaterial should have a softening or melting point that lies solved in Sovol(chlorinated biphenyl). close to the temperature at. which the polyimide is being The resultant polyarylate is dissolved in chloroform to obprocessed. tain a 5 percent solution and thereafter precipitated with a The polyarylates employed as an antifriction material comfive-fold excess of methyl alcohol, filtered off and dried at a ponent are prepared from aromatic dicarboxylic acid tempe ature of 12 C- for 6 h urs. chlorides and bisphenols in a high-boiling solvent by the The components are mixed in a vibrating mill to give a equilibrium high-temperature polycondensation method. The moulding composition, which is thereafter moulded at a tempolyarylates thus obtained are precipitated with an excess of perature of 390-4 10 C. and a specific pressure of 1,000 to solvent, filtered off and dried to constant weight. 1,200 kg./cm.".
The antifriction material prepared as disclosed hereinbefore exhibits the following physical and mechanical characteristics:
Brincll hardness. kgjmm. 20 Impact strength. kg./cm./cm. 3 intensity of linear wear IXIO Coefficient of friction 0.12 Maximum working temperature. C. 240
EXAMPLE 2 A Polymide of the general formula derived from diphenyl oxide 3,3',4,4'-tetracarboxylic acid dianhydride and m-phenylene diamine, and a polyarylate of the general formula V M I derived from terephthaloyl dichloride and dihydroxydiphenylfluorene are prepared as disclosed in example 1.
37.5 g. of the powdered polyimide, 12.5 g. of the powdered polyarylate and 450 g. of powdered molybdenum disulfide (particle size, 1-2,u) are mixed in a vibrating mill for a period of 2 minutes to obtain a homogeneous mass.
The moulding composition thus prepared is subjected to moulding at a temperature of 490500 C. and a specific pressure of 1.000 to 1,200 kg./cm.
The antifriction material exhibits the following physical and mechanical characteristics:
Brinell hardness, kg/mm. 21 Impact strength. kg.cm./cm.' 2 Intensity of linear wear 1.3Xl()" Coefficient of linear wear 0.12 Maximum working temperature. C. 260
EXAMPLE 3 Fifty grams of powdered a polyimide prepared as disclosed in example 1 is mixed in a vibrating mill with 420 g. of graphite powder and 20 g. of polymetaphenylene isophthalamide ofthe structural formula Intensity oflinear wear 0.9x 10' Coefficicnt of friction 0.1 Maximum working temperature. C. 250
EXAMPLE 4 37.5 g. of powdered polyimide prepared as disclosed in example 2 is mixed in a vibrating mill for a period of 2 minutes with 450 g. of graphite powder and 12.5 g. of polyamide havl0 ing the structural formula II 0 h 20 the polyamide being synthesized from anilinephthalein and isophthalic acid by the method disclosed in example 3.
The moulding powder thus obtained is moulded at a temperature of 490-500 C. and under a specific pressure of 1,000 to 1,200 kg./cm.
The antifriction material exhibits the following physical and mechanical characteristics:
Intensity oflincar wear 0.9Xl0 Coefficicnt of friction 0.1 Maximum working temperature. C. 270
EXAMPLE 5 37.5 g. of powdered polyimide and 12.5 g. of polyarylate prepared as disclosed in example 1, 325 g. of molybdenum disulftde powder (particle size, l-2y.), and 125 g. of copper powder are blended in a vibrating mill for a period of 2 minutes.
The moulding composition thus obtained is moulded at a temperature of 3904l0 C. and under specific pressure of 1,000 to 1.200 kg./cm.
The antifriction material exhibits the following physical and mechanical characteristics:
Brinell hardness. kgjmm. 24 Impact strength. kg.cm./em. 2.5 Coefficient of friction 0.1 N Maximum working temperature, C. 250
EXAMPLE 6 37.5 g. of powdered polyimide prepared as disclosed in example 1. 12.5 g. of polyamide prepared by the procedure of example 3, 325 g. of molybdenum disulfide powder (particle size. 1-2u), and 125 g. of silver powder are mixed in a vibrating mill for a period of 2 minutes.
The moulding composition thus obtained is subjected to compression moulding at a temperature of 3904l0 C. and under specific pressure of 1,000 to 1,200 kg./cm.
The antifriction material exhibits the following physical and mechanical characteristics:
Brinell hardness. kgJmm. Z2 Intensity of linear wcar (1.7X10 Maximum working temperature. "C. 250
Although the present invention has been described with reference to the preferred embodiment thereof, it will be readily understood by those skilled in the art that various changes and modifications can be practised without departing from the spirit and scope of the invention as disclosed in the description and appended claims.
We claim:
1. An antifriction material having a stable coefficient of friction over a wide temperature range comprising 1. 4 to 78 percent by weight of one or more aromatic polyimide resins prepared by polycondensation of an aromatic diamine with an aromatic tetracarboxylic acid dianhydride to yield a polyamido carboxylic acid which after being subjected to polycyclization gives a polyimide,
2. 2 to 75 percent by weight of one or more solid inorganic lubricants, and
3. l to percent by weight of one or more rigid-chain polymers selected from the group consisting of a) polyarylates prepared by polycondensation of aromatic dicarboxylic acid chlorides and bisphenols and (b) aromatic polyamides prepared by polycondensation of aromatic diamines and aromatic dicarboxylic acids or their chlorides.
2. An antifriction material as in claim 1 which further comprises a powdered metal filler.
3. An antifriction material as in claim 2 which comprises 4 to 78 percent of polyimide resin, 2 to 78 percent by weight of solid lubricants, 20 to 40 percent by weight of powdered metal filler, and l to 20 percent by weight of the polyarylate or aro- 6 matic polyamide polymer.
4. An antifriction material as in claim 1 wherein the polyimide is prepared from diphenyl oxide 3,3, 4, 4-tetracarbox' ylic dianhydride and a diamine selected from the group consisting of 4,4-diaminodiphenyl ether and m-phenylenediamine.
5. An antifriction material as in claim 1 wherein the polyarylate is prepared from terephthaloyl chloride and a bisphenol selected from the group consisting of phenolphthalein and dihydroxydiphenyl fluorene.
6. An antifriction material as in claim 1 wherein the polyamide is prepared from isophthaloyl dichloride and an amine selected from the group consisting of m-phenylenediamine and anilinephthalein.
7. An antifriction material as in claim 1 wherein the solid lubricant is selected from the group consisting of molybdenum disulfide and graphite.
8. An antifriction material as in claim 2 wherein the metal is copper or silver.
Claims (9)
- 2. 2 to 75 percent by weight of one or more solid inorganic lubricants, and
- 2. An antifriction material as in claim 1 which further comprises a powdered metal filler.
- 3. 1 to 20 percent by weight of one or more rigid-chain polymers selected from the group consisting of (a) polyarylates prepared by polycondensation of aromatic dicarboxylic acid chlorides and bisphenols and (b) aromatic polyamides prepared by polycondensation of aromatic diamines and aromatic dicarboxylic acids or their chlorides.
- 3. An antifriction material as in claim 2 which comprises 4 to 78 percent of polyimide resin, 2 to 78 percent by weight of solid lubricants, 20 to 40 percent by weight of powdered metal filler, and 1 to 20 percent by weight of the polyarylate or aromatic polyamide polymer.
- 4. An antifriction material as in claim 1 wherein the polyimide is prepared from diphenyl oxide 3,3'', 4, 4'' -tetracarboxylic dianhydride and a diamine selected from the group consisting of 4,4''-diaminodiphenyl ether and m-phenylenediamine.
- 5. An antifriction material as in claim 1 wherein the polyarylate is prepared from terephthaloyl chloride and a bisphenol selected from the group consisting of phenolphthalein and dihydroxydiphenyl fluorene.
- 6. An antifriction material as in claim 1 wherein the polyamide is prepared from isophthaloyl dichloride and an amine selected from the group consisting of m-phenylenediamine and anilinephthalein.
- 7. An antifriction material as in claim 1 wherein the solid lubricant is selected from the group consisting of molybdenum disulfide and graphite.
- 8. An antifriction material as in claim 2 wherein the metal is copper or silver.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83578569A | 1969-06-23 | 1969-06-23 | |
GB33616/69A GB1244427A (en) | 1969-06-23 | 1969-07-03 | Antifriction material |
Publications (1)
Publication Number | Publication Date |
---|---|
US3629103A true US3629103A (en) | 1971-12-21 |
Family
ID=26261943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US835785A Expired - Lifetime US3629103A (en) | 1969-06-23 | 1969-06-23 | Plastic antifriction material |
Country Status (2)
Country | Link |
---|---|
US (1) | US3629103A (en) |
GB (1) | GB1244427A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3928673A (en) * | 1973-08-16 | 1975-12-23 | Ball Brothers Res Corp | Release and lubricating composition for glass molds and method and apparatus utilizing such composition |
US4075111A (en) * | 1976-04-19 | 1978-02-21 | Hughes Aircraft Company | Heavy metal chalcogenide-polyimide lubricative composites |
US4076634A (en) * | 1974-10-28 | 1978-02-28 | Vasily Vladimirovich Korshak | Composition for antifriction material |
US4371445A (en) * | 1979-03-14 | 1983-02-01 | Heinz Faigle Kg | Arrangement in pairs of plastic sliding on plastic in tribologic systems |
FR2537990A1 (en) * | 1982-12-17 | 1984-06-22 | Kobe Steel Ltd | Film of lubricant and process for preventing chafing of sliding metal surfaces |
US4532054A (en) * | 1982-12-28 | 1985-07-30 | General Electric Company | Polyetherimide bearing compositions |
WO1998007785A1 (en) * | 1996-08-19 | 1998-02-26 | E.I. Du Pont De Nemours And Company | Polyimide polymeric blends |
US10711526B2 (en) | 2017-02-01 | 2020-07-14 | Baker Hughes, A Ge Company, Llc | Methods for forming or servicing a wellbore, and methods of coating surfaces of tools |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0122305A1 (en) * | 1983-04-15 | 1984-10-24 | General Electric Company | Polyetherimide-polyamide blends |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2698966A (en) * | 1951-09-27 | 1955-01-11 | Polymer Corp | Process for producing shaped articles from mixtures of polyamides |
US3122505A (en) * | 1961-04-11 | 1964-02-25 | Dixon Corp | Bearing composition |
US3287288A (en) * | 1964-09-21 | 1966-11-22 | Duriron Co | Low friction composition containing a resinous binder and degraded polytetrafluoroethylene particles |
-
1969
- 1969-06-23 US US835785A patent/US3629103A/en not_active Expired - Lifetime
- 1969-07-03 GB GB33616/69A patent/GB1244427A/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2698966A (en) * | 1951-09-27 | 1955-01-11 | Polymer Corp | Process for producing shaped articles from mixtures of polyamides |
US3122505A (en) * | 1961-04-11 | 1964-02-25 | Dixon Corp | Bearing composition |
US3287288A (en) * | 1964-09-21 | 1966-11-22 | Duriron Co | Low friction composition containing a resinous binder and degraded polytetrafluoroethylene particles |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3928673A (en) * | 1973-08-16 | 1975-12-23 | Ball Brothers Res Corp | Release and lubricating composition for glass molds and method and apparatus utilizing such composition |
US4076634A (en) * | 1974-10-28 | 1978-02-28 | Vasily Vladimirovich Korshak | Composition for antifriction material |
US4075111A (en) * | 1976-04-19 | 1978-02-21 | Hughes Aircraft Company | Heavy metal chalcogenide-polyimide lubricative composites |
US4371445A (en) * | 1979-03-14 | 1983-02-01 | Heinz Faigle Kg | Arrangement in pairs of plastic sliding on plastic in tribologic systems |
FR2537990A1 (en) * | 1982-12-17 | 1984-06-22 | Kobe Steel Ltd | Film of lubricant and process for preventing chafing of sliding metal surfaces |
US4532054A (en) * | 1982-12-28 | 1985-07-30 | General Electric Company | Polyetherimide bearing compositions |
WO1998007785A1 (en) * | 1996-08-19 | 1998-02-26 | E.I. Du Pont De Nemours And Company | Polyimide polymeric blends |
CN1098310C (en) * | 1996-08-19 | 2003-01-08 | 纳幕尔杜邦公司 | Polyimide polymeric blends |
US10711526B2 (en) | 2017-02-01 | 2020-07-14 | Baker Hughes, A Ge Company, Llc | Methods for forming or servicing a wellbore, and methods of coating surfaces of tools |
Also Published As
Publication number | Publication date |
---|---|
GB1244427A (en) | 1971-09-02 |
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