[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

EP0000697B1 - A lubricating composition in the form of a gel consisting of an oil and polymethylpentene - Google Patents

A lubricating composition in the form of a gel consisting of an oil and polymethylpentene Download PDF

Info

Publication number
EP0000697B1
EP0000697B1 EP78100269A EP78100269A EP0000697B1 EP 0000697 B1 EP0000697 B1 EP 0000697B1 EP 78100269 A EP78100269 A EP 78100269A EP 78100269 A EP78100269 A EP 78100269A EP 0000697 B1 EP0000697 B1 EP 0000697B1
Authority
EP
European Patent Office
Prior art keywords
oil
temperature
lubricating
pmp
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
EP78100269A
Other languages
German (de)
French (fr)
Other versions
EP0000697A1 (en
Inventor
John Ronald Rumiers
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SKF Industries Inc
Original Assignee
SKF Industries Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SKF Industries Inc filed Critical SKF Industries Inc
Publication of EP0000697A1 publication Critical patent/EP0000697A1/en
Application granted granted Critical
Publication of EP0000697B1 publication Critical patent/EP0000697B1/en
Expired legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/02Parts of sliding-contact bearings
    • F16C33/04Brasses; Bushes; Linings
    • F16C33/06Sliding surface mainly made of metal
    • F16C33/10Construction relative to lubrication
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • C10M111/04Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M143/00Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
    • C10M143/08Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation containing aliphatic monomer having more than 4 carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • Scott and Swartz U.S. Patent 3,913,992 issued October 21, 1975, discloses a method and apparatus employing a mass of grease placed on a dispensing surface on a rotating member in such a way that the centrifugal force of the grease against the dispensing surface causes oil to be released from the grease under use conditions.
  • the DOS 1,900,168 teaches a process for thickening oil by heating a specified dispersion of a polymer in oil to a temperature of 130-170°C.
  • the size of the particles dispersed shall be in the range 0,02-0,5 microns. This process does not give any solid gel, but results in a highly viscous grease.
  • a process for the production of a solid lubricating gel which is characterized in blending 50-10% by weight of a polymethylpentene having an average molecular weight of 3.5 millions and a particle size of 105-250 microns with 50-90% by weight and an oil of lubricating viscosity, heating said blend at a temperature in the range of 10-50°C above the initial softening temperature of the polymer until the blend becomes transparent and sticky, and cooling the blend.
  • the oil is preferably a synthetic hydrocarbon oil with a viscosity of 15 to 300 mm 2 /s at 38°C.
  • the oil content is preferably in the range of 65-75% by weight, and the polymethylpentene content is in the range of 35-25% by weight.
  • the most preferred ratio on the components is an oil content of 70% by weight and a polymethylpentene content of 30% by weight.
  • the oil shall then have a viscosity of 30-170 mm 2 /s at 38°C and the polymethylpentene an average molecular weight of 4 millions.
  • compositions obtained through the process according to the invention are provided in the form of firm, tough, solid gels having an oily surface provided by the exudation of oil from the gels.
  • compositions of the invention are made from synthetic hydrocarbon oils having a viscosity in the range from about 20 to about 260 mm 2 /s measured at a temperature of 38°C (100°F).
  • Other known lubricating oils of comparable viscosity may also be employed including the diester oils described in Military Specifications MIL-L-23699B and MIL-L-7808G. These refer to aircraft turbine engine lubricants. Products qualified under these specifications are (respectively) Exxon ETO 2380 and Exxon ETO 2389.
  • Naturally occurring mineral oils may also be employed, but less desirably, since they tend to deteriorate at the high temperatures employed in the preparation of the new lubricating compositions.
  • Especially preferred compositions are obtained from synthetic hydrocarbon oils having a viscosity in the range from about 30 to about 170 mm 2 /s.
  • the polymeric component of the new compositions is known in commerce as polymethylpentene (hereinafter PMP) and generally has an average molecular weight in the range from about 3 to about 5 million; polymer having an average molecular weight of about 4 million having been found to provide excellent products.
  • PMP polymethylpentene
  • This material is available and useful in finely particulate form, i.e. about 105 to 250 microns.
  • the PMP is simply blended with the oil in a conventional blender to form a physical mixture.
  • this mixture may contain about 50 to about 90% oil and about 50 to about 10% PMP, based on the weight of the total mixture.
  • Preferred proportions are about 65 to about 75% oil and about 35 to about 25% PMP; especially desirable products contain about 70% oil and about 30% PMP in the mixture and in the final product.
  • the physical mixture of oil and PMP is then introduced to a mold or into the cavity of a bearing or other article in which it is desired to produce a lubricating mass in situ.
  • the mixture is then cured by heating it to a temperature in the range from about 220°C (428°F) to about 260°C (500°F); the exact temperature in the range from about 10°C (18°F) to about 50°C (90°F) above the initial softening temperature of the particular PMP polymer in the mixture, depending on the liquid phase used.
  • This curing temperature is maintained for about 45 to about 75 minutes until the mixture becomes transparent and sticky. This end point may be determined visually, by trial and error, or by testing the mixture with a metal rod to which the mixture will adhere when properly cured.
  • the final product is then obtained by allowing the cured mixture to cool whereupon it forms a firm, tough, solid gel conforming in shape to the mold or cavity of a bearing or other article in which it was heated.
  • the shaped lubricating mass is formed in situ in a bearing, for example, it is used in that form.
  • Molded shaped articles may be shaped further, if desired, by conventional cutting, abrading or other procedures.
  • the resulting composition or article has an oily surface provided by the exudation of oil from the gel. This exudation of oil continues until the oil supply is exhausted, thus providing prolonged lubrication of any surface in contact with the gel.
  • the new compositions have been found capable of withstanding prolonged use at operating temperatures of up to 145°C (293°F) and, for shorter periods, at up to 160°C (320°F).
  • the oil-polyethylene gel lubricating compositions of the prior art are inoperable at such elevated temperatures, since they become sticky and are discharged from bearings, leaving a dry bearing, at operating temperatures of only about 105°C (221°F) to 110°C (230°F). It will be apparent to those skilled in the art, therefore, that the new PMP containing lubricant compositions and articles constitute a distinct improvement over the prior art for use at operating temperatures above 105°C (221°F).
  • the physical characteristics of the gels of the present invention vary somewhat depending upon the average molecular weight of the PMP and the proportion of that material in the final lubricating composition. Increasing the molecular weight and concentration of PMP in the composition increases the firmness, toughness and rigidity of the gel. These characteristics are correspondingly decreased by decreasing the molecular weight and concentration of the PMP in the composition. It will be seen, therefore, that by varying the molecular weight and concentration of the PMP, lubricating compositions can be produced which are especially adapted for use in particular application.
  • a shaped mass of lubricating gel was prepared containing 70% oil and 30% PMP by weight of the total composition. More specifically 40 grams of PMP was mixed with 93 grams of lubricating oil in a conventional blender for about one minute until a homogeneous mixture was obtained.
  • the PMP was in the form of a 105-215 microns powder which is commercially available under the trade name "TPX Polymer” from Mitsui Petrochemical Inudstries, Mitsui Et Company Incorporated. This PMP has an average molecular weight of 4 million.
  • the oil was a synthetic hydrocarbon oil available from Mobil Oil Corporation under the trade name "SHC624" and had a viscosity of 33 m 2 /s at 38°C (100°F).
  • the oil-PMP mixture was charged to suitable mold with provision for heating, heated to 218°C (425°F) and maintained at that temperature for 60 minutes. The end is reached when the mixture becomes transparent and self-cohesive.
  • Example 1 The general procedure of Example 1 was repeated with the exception that 10% PMP was mixed with 90% Mobil SHC624. The resulting shaped lubricating gel mass was similar to that obtained in Example 1 but was much more flexible due to the decreased percentage of polymer present.
  • Example 2 The general procedure of Example 2 was repeated with the exception that 50% PMP was mixed with 50% Mobil SHC624. The cure temperature was again 218°C (425°F). However, the end point was not obtained until 180 minutes of cure, the resulting shaped lubricating gel mass was similar to that obtained in Example 1 but was much harder and less oil exuding. These effects are attributable to the increase in polymer content.
  • Example 3A The general procedure of Example 3A was repeated with the exception that the cure was 232°C (450°F) for one hour. A similar lubricating gel mass was obtained. The reduction in curing time was related to the increase in curing temperature.
  • Example 1 The general procedure of Example 1 was repeated using the same PMP but substituting Mobil "SHC 629" for the oil used previously. This oil differs primarily in having a viscosity of 160 mm 2 /s at 38°C (100°F). No end point of the cure cycle was reached after 240 minutes using a 218°C (425°F) cure temperature. No shaped mass was formed. This is attributable to the greatly increased viscosity of the lubricant which hinders intimate mixing during the cure cycle at 218°C (425°F).
  • Example 4 The general procedure of Example 4 was repeated except a cure temperature of 254°C (490 0 F) was employed. An end point was reached in 45-50 minutes. The resulting shaped lubricating gel was similar to that obtained in Example 1.
  • Example 1 The general procedure of Example 1 was repeated with the exception that diester lubricant Exxon 2380 was substituted for the previously used oil.
  • the cure cycle was 252°C (485°F) for 60 minutes.
  • the resultant shaped mass was obtained in the form of a tough, resilient solid gel with an oily surface caused by the exudation of oil from the gel.
  • Example 2 The general procedure of Example 1 was repeated with the exception that Mobil DTE XH, a mineral oil based lubricant, with a viscosity of 138 mm 2 /s at 38°C (100°F) was substituted for the previously used oil.
  • Mobil DTE XH a mineral oil based lubricant, with a viscosity of 138 mm 2 /s at 38°C (100°F) was substituted for the previously used oil.
  • the resultant shaped mass was grainy and discolored due to substantial oxidation of the Mobil DTE XH.
  • the speed of rotation of the inner ring of the bearing was increased step-wise in 3600 rpm increments, allowing the apparatus to run until the operating temperature had stabilized at each step. No extraneous heat was supplied, i.e. the test was run under ambient temperature conditions.
  • the bearing speed reached 7200 rpm at which speed the oil-polyethylene gel lubricant failed by the lubricant mass being expelled from the bearing.
  • the bearing temperature was 49°C (120°F) at 7200 rpm.
  • oils of lubricating viscosity in the range of 15 to 300 mm 2 /s or more can be employed in the compositions of the present invention.
  • the invention is operable with lubricants having a mineral oil base, diester oil base, or synthetic hydrocarbon oil base and all three types are represented in the examples.
  • the PMP-oil mixtures can be stabilized so that they may be shipped in that form prior to being fully gelled by the purchaser or final user. This is done by partially curing the PMP-oil mixture by heating to a temperature of about 28° to 42°C (50° to 75°F) below the curing temperature of the particular mixture and maintaining this temperature for a period of about 15 to 20 minutes to form a partially gelled and stabilized product of grease-like consistency. After shipping and/or storage such stabilized products are curable in the usual way to provide the shaped relatively rigid gels of the invention.
  • the PMP oil mixture of Example 5, containing Mobil SHC 629 which cured at 254°C (490°F) would be heated to about 224°C (435°F) for 15 to 20 minutes to obtain a stabilized mixture for shipping.
  • the curing temperature of the PMP-oil mixtures varies somewhat depending on the identity of the particular oil and its viscosity. In general the higher the viscosity of the oil, the higher the temperature required to achieve an adequate cure.
  • the optimum curing temperature for any particular PMP-oil mixture can of course, be determined by trial and error or by experience. Inasmuch as the compositions of the present invention are curable at temperatures within the range of about 220°C (428°F) to about 260°C (500°F), they may be stabilized by heating for 15 to 20 minutes at temperature within the range from about 178°C (353°F) to about 218°C (425°F).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Lubricants (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

    Background of the invention
  • It has long been recognized that it would be desirable in many industries and arts to provide a lubricating product which would be capable of releasing lubricant over a prolonged period of time under use conditions. For example, self- lubricating bearings are of great value in the automotive, aviation and other industries. It has also been recognized that it would be highly desirable for such lubricants to be self-supporting, i.e. to have sufficient inherent mechanical strength to actually constitute or at least form a sort of the lubricating structure.
  • The prior art
  • Self-supporting lubricating compositions and articles and methods for producing them have been described in the prior art. For example, Davis and Gilles U.S. Patents: 3,729,415, issued April 24, 1973; 3,547,819, issued December 15, 1970; and 3,541,011, issued November 17, 1970; all disclose lubricating compositions comprising a hydrocarbon oil and polyethylene in various forms, including self-supporting gels which exude oil and thus have an oily lubricating surface. British Patent 1,173,123 published September 4, 1969, is based on the foregoing Davis and Gilles U.S. Patents, but suggests that polyolefins other than polyethylene, such as polypropylene and polybutylene may be used in such compositions, although all of the working examples actually employ only polyethylene.
  • Agens U.S. Patent 3,135,564, issued June 2, 1964, discloses an anti-friction bearing and a method of making it which contains a formed- in-place, unitary, solid, plastisol containing a lubricant completely filling an annular space to provide lubrication.
  • Scott and Swartz U.S. Patent 3,913,992, issued October 21, 1975, discloses a method and apparatus employing a mass of grease placed on a dispensing surface on a rotating member in such a way that the centrifugal force of the grease against the dispensing surface causes oil to be released from the grease under use conditions.
  • The DOS 1,900,168 teaches a process for thickening oil by heating a specified dispersion of a polymer in oil to a temperature of 130-170°C. The size of the particles dispersed shall be in the range 0,02-0,5 microns. This process does not give any solid gel, but results in a highly viscous grease.
  • It will be ssen from the foregoing that self-supporting lubricating compositions and articles such as bearings containing them have been developed previously. However, the existing compositions of this type have been found to be useful only at operating temperatures no higher than about 105°C (221 °F), since they become tacky, lose their lubricity and are discharged leaving a dry bearing at temperatures of about 110°C (230°F) or higher.
  • It is a primary object of the present invention to provide a process for the production of improved lubricating compositions capable of providing lubrication for prolonged periods of time at operating temperatures above 105°C (221 °F).
  • Brief description of the invention
  • According to the present invention one has brought about a process for the production of a solid lubricating gel which is characterized in blending 50-10% by weight of a polymethylpentene having an average molecular weight of 3.5 millions and a particle size of 105-250 microns with 50-90% by weight and an oil of lubricating viscosity, heating said blend at a temperature in the range of 10-50°C above the initial softening temperature of the polymer until the blend becomes transparent and sticky, and cooling the blend.
  • It is advantageous to heat the blend at a temperature of 220-260°C in a period of 45 to 75 minutes.
  • The oil is preferably a synthetic hydrocarbon oil with a viscosity of 15 to 300 mm2/s at 38°C.
  • The oil content is preferably in the range of 65-75% by weight, and the polymethylpentene content is in the range of 35-25% by weight.
  • The most preferred ratio on the components is an oil content of 70% by weight and a polymethylpentene content of 30% by weight. The oil shall then have a viscosity of 30-170 mm2/s at 38°C and the polymethylpentene an average molecular weight of 4 millions.
  • The compositions obtained through the process according to the invention are provided in the form of firm, tough, solid gels having an oily surface provided by the exudation of oil from the gels.
  • The preferred compositions of the invention are made from synthetic hydrocarbon oils having a viscosity in the range from about 20 to about 260 mm2/s measured at a temperature of 38°C (100°F). Other known lubricating oils of comparable viscosity may also be employed including the diester oils described in Military Specifications MIL-L-23699B and MIL-L-7808G. These refer to aircraft turbine engine lubricants. Products qualified under these specifications are (respectively) Exxon ETO 2380 and Exxon ETO 2389.
  • Naturally occurring mineral oils may also be employed, but less desirably, since they tend to deteriorate at the high temperatures employed in the preparation of the new lubricating compositions. Especially preferred compositions are obtained from synthetic hydrocarbon oils having a viscosity in the range from about 30 to about 170 mm2/s.
  • The polymeric component of the new compositions is known in commerce as polymethylpentene (hereinafter PMP) and generally has an average molecular weight in the range from about 3 to about 5 million; polymer having an average molecular weight of about 4 million having been found to provide excellent products. This material is available and useful in finely particulate form, i.e. about 105 to 250 microns.
  • In preparing the new compositions, the PMP is simply blended with the oil in a conventional blender to form a physical mixture. As noted above, this mixture may contain about 50 to about 90% oil and about 50 to about 10% PMP, based on the weight of the total mixture. Preferred proportions are about 65 to about 75% oil and about 35 to about 25% PMP; especially desirable products contain about 70% oil and about 30% PMP in the mixture and in the final product.
  • The physical mixture of oil and PMP is then introduced to a mold or into the cavity of a bearing or other article in which it is desired to produce a lubricating mass in situ. The mixture is then cured by heating it to a temperature in the range from about 220°C (428°F) to about 260°C (500°F); the exact temperature in the range from about 10°C (18°F) to about 50°C (90°F) above the initial softening temperature of the particular PMP polymer in the mixture, depending on the liquid phase used. This curing temperature is maintained for about 45 to about 75 minutes until the mixture becomes transparent and sticky. This end point may be determined visually, by trial and error, or by testing the mixture with a metal rod to which the mixture will adhere when properly cured. The final product is then obtained by allowing the cured mixture to cool whereupon it forms a firm, tough, solid gel conforming in shape to the mold or cavity of a bearing or other article in which it was heated. Where the shaped lubricating mass is formed in situ in a bearing, for example, it is used in that form. Molded shaped articles may be shaped further, if desired, by conventional cutting, abrading or other procedures. The resulting composition or article has an oily surface provided by the exudation of oil from the gel. This exudation of oil continues until the oil supply is exhausted, thus providing prolonged lubrication of any surface in contact with the gel. The new compositions have been found capable of withstanding prolonged use at operating temperatures of up to 145°C (293°F) and, for shorter periods, at up to 160°C (320°F). The oil-polyethylene gel lubricating compositions of the prior art, on the other hand, are inoperable at such elevated temperatures, since they become sticky and are discharged from bearings, leaving a dry bearing, at operating temperatures of only about 105°C (221°F) to 110°C (230°F). It will be apparent to those skilled in the art, therefore, that the new PMP containing lubricant compositions and articles constitute a distinct improvement over the prior art for use at operating temperatures above 105°C (221°F).
  • The physical characteristics of the gels of the present invention vary somewhat depending upon the average molecular weight of the PMP and the proportion of that material in the final lubricating composition. Increasing the molecular weight and concentration of PMP in the composition increases the firmness, toughness and rigidity of the gel. These characteristics are correspondingly decreased by decreasing the molecular weight and concentration of the PMP in the composition. It will be seen, therefore, that by varying the molecular weight and concentration of the PMP, lubricating compositions can be produced which are especially adapted for use in particular application.
  • Detailed description of the invention Example 1
  • To illustrate the preferred practice of the invention a shaped mass of lubricating gel was prepared containing 70% oil and 30% PMP by weight of the total composition. More specifically 40 grams of PMP was mixed with 93 grams of lubricating oil in a conventional blender for about one minute until a homogeneous mixture was obtained. The PMP was in the form of a 105-215 microns powder which is commercially available under the trade name "TPX Polymer" from Mitsui Petrochemical Inudstries, Mitsui Et Company Incorporated. This PMP has an average molecular weight of 4 million. The oil was a synthetic hydrocarbon oil available from Mobil Oil Corporation under the trade name "SHC624" and had a viscosity of 33 m2/s at 38°C (100°F).
  • After blending, the oil-PMP mixture was charged to suitable mold with provision for heating, heated to 218°C (425°F) and maintained at that temperature for 60 minutes. The end is reached when the mixture becomes transparent and self-cohesive.
  • Heating was then discontinued and the mold and its contents allowed to cool to ambient temperature. When the mold was opened, a self-supporting, shaped mass of lubricating composition was obtained in the form of a firm, tough, solid gel having an oily surface caused by exudation of oil from the gel.
  • Example 2
  • The general procedure of Example 1 was repeated with the exception that 10% PMP was mixed with 90% Mobil SHC624. The resulting shaped lubricating gel mass was similar to that obtained in Example 1 but was much more flexible due to the decreased percentage of polymer present.
  • Example 3A
  • The general procedure of Example 2 was repeated with the exception that 50% PMP was mixed with 50% Mobil SHC624. The cure temperature was again 218°C (425°F). However, the end point was not obtained until 180 minutes of cure, the resulting shaped lubricating gel mass was similar to that obtained in Example 1 but was much harder and less oil exuding. These effects are attributable to the increase in polymer content.
  • Example 3B
  • The general procedure of Example 3A was repeated with the exception that the cure was 232°C (450°F) for one hour. A similar lubricating gel mass was obtained. The reduction in curing time was related to the increase in curing temperature.
  • Example 4
  • The general procedure of Example 1 was repeated using the same PMP but substituting Mobil "SHC 629" for the oil used previously. This oil differs primarily in having a viscosity of 160 mm2/s at 38°C (100°F). No end point of the cure cycle was reached after 240 minutes using a 218°C (425°F) cure temperature. No shaped mass was formed. This is attributable to the greatly increased viscosity of the lubricant which hinders intimate mixing during the cure cycle at 218°C (425°F).
  • Example 5
  • The general procedure of Example 4 was repeated except a cure temperature of 254°C (4900F) was employed. An end point was reached in 45-50 minutes. The resulting shaped lubricating gel was similar to that obtained in Example 1.
  • Example 6
  • The general procedure of Example 1 was repeated with the exception that diester lubricant Exxon 2380 was substituted for the previously used oil. The cure cycle was 252°C (485°F) for 60 minutes. The resultant shaped mass was obtained in the form of a tough, resilient solid gel with an oily surface caused by the exudation of oil from the gel.
  • Example 7
  • The general procedure of Example 1 was repeated with the exception that Mobil DTE XH, a mineral oil based lubricant, with a viscosity of 138 mm2/s at 38°C (100°F) was substituted for the previously used oil. The resultant shaped mass was grainy and discolored due to substantial oxidation of the Mobil DTE XH.
  • Example 8
  • A functional test was designed in order to assess the relative merits of the new lubricating compositions and similar oil-polyethylene lubricating gels of the prior art. A standard 6205 Ball bearing having a fixed outer ring and a rotatable inner ring was provided with an intermediate lubricant mass to be tested having a surface in contact with the rotating inner ring. This apparatus was then used in a series of tests as follows:
    • (a) The bearing was loaded with a lubricating mass consisting of an oil-polyethylene gel of the prior art such as those described in Davis and Gillies U.S. Patent 3,541,011. The exact composition of the gel was 30% polyethylene (Hercules UHMW 1900) and 70% Mobil DTE XH oil.
  • The speed of rotation of the inner ring of the bearing was increased step-wise in 3600 rpm increments, allowing the apparatus to run until the operating temperature had stabilized at each step. No extraneous heat was supplied, i.e. the test was run under ambient temperature conditions.
  • The bearing speed reached 7200 rpm at which speed the oil-polyethylene gel lubricant failed by the lubricant mass being expelled from the bearing. The bearing temperature was 49°C (120°F) at 7200 rpm.
    • (b) The foregoing procedure was repeated after substituting an oil-PMP lubricant gel of Example 5 in the bearing. The bearing was run at 3600 rpm, 7200 rpm, and 8500 rpm with the bearing temperature allowed to stabilize at each step. Lubricant failure occurred after 1,5 hours running at 8500 rpm and a bearing temperature of 110°C (230°F), indicating that the oil-PMP lubricating compositions are as good as or better than, the oil-polyethylene gels of the prior art under ambient conditions.
    • (c) The same standard 6205 ball bearing was charged with an oil-polyethylene lubricating mass of 30% polyethylene and 70% Mobil DTE XH oil and a test was conducted at a constant bearing speed of 3600 rpm under a thrust load of 665 newton (150 lbs). In this test, however, the operating temperature was increased in discrete steps after ambient running for 72 hours. The extraneous heat was supplied by mounting the bearing in a housing containing electrical cartridge heaters which riased the temperature of the bearing outer ring.
  • Under these conditions the oil-polyethylene lubricant composition of the prior art failed upon reaching a temperature of 100°C (212°F).
    • (d) The procedure of Example 8(c) was repeated substituting an oil-PMP lubricating mass according to Example 5. In this test the bearing was run at ambient temperature for 140 hours. Then the temperature was raised in controlled increments over a period of four hours until an operating temperature of 149°C (300°F) was reached. The bearing was permitted to run for an additional 670 hours at a speed of 3600 rpm and 149°C (300°F) operating temperature before terminating the test, without failure.
  • It is clear from the foregoing that the oil-PMP lubricating compositions of the present invention are markedly superior to the oil-polyethylene compositions of the prior art at operating temperatures above 93°C (200°F).
  • It will be apparent to those skilled in the art that a wide variety of oils of lubricating viscosity in the range of 15 to 300 mm2/s or more can be employed in the compositions of the present invention. The invention is operable with lubricants having a mineral oil base, diester oil base, or synthetic hydrocarbon oil base and all three types are represented in the examples.
  • One of the advantages of the present invention is that the PMP-oil mixtures can be stabilized so that they may be shipped in that form prior to being fully gelled by the purchaser or final user. This is done by partially curing the PMP-oil mixture by heating to a temperature of about 28° to 42°C (50° to 75°F) below the curing temperature of the particular mixture and maintaining this temperature for a period of about 15 to 20 minutes to form a partially gelled and stabilized product of grease-like consistency. After shipping and/or storage such stabilized products are curable in the usual way to provide the shaped relatively rigid gels of the invention. For example, the PMP oil mixture of Example 5, containing Mobil SHC 629 which cured at 254°C (490°F) would be heated to about 224°C (435°F) for 15 to 20 minutes to obtain a stabilized mixture for shipping.
  • The curing temperature of the PMP-oil mixtures varies somewhat depending on the identity of the particular oil and its viscosity. In general the higher the viscosity of the oil, the higher the temperature required to achieve an adequate cure. The optimum curing temperature for any particular PMP-oil mixture can of course, be determined by trial and error or by experience. Inasmuch as the compositions of the present invention are curable at temperatures within the range of about 220°C (428°F) to about 260°C (500°F), they may be stabilized by heating for 15 to 20 minutes at temperature within the range from about 178°C (353°F) to about 218°C (425°F).
  • It should be understood that all proportions herein are expressed in percentages based on the total oil and PMP content, not including any additives which may be present.

Claims (7)

1. A process for the production of a solid lubricating gel characterized in blending 50-10% by weight of a polymethylpentene having an average molecular weight of 3-5 millions and a particle size of 105-250 microns with 50-90% by weight of an oil of lubricating viscosity, heating said blend at a temperature in the range of 10-50°C above the initial softening temperature of the polymer until the blend becomes transparent and sticky, and cooling the blend.
2. A process according to claim 1 characterized in that the blend is heated at a temperature of 220-260°C in a period of 45-75 minutes.
3. A process according to claim 1, characterized in that the oil is a synthetic hydrocarbon oil.
4. A process according to claim 3, characterized in that the oil has a viscosity of 15-300 mm2/s at 38°C.
5. A process according to claim 4 characterized in that the oil content is 65-75% by weight and the polymethylpentene is 35-25% by weight.
6. A process according to claim 4, characterized in that the oil content is 70% by weight and the polymethylpentene is 30% by weight.
7. A process according to claim 4, characterized in that the oil has a viscosity of 30-170 mm2/s and the polymethylpentene has an average molecular weight of 4 millions.
EP78100269A 1977-07-20 1978-06-29 A lubricating composition in the form of a gel consisting of an oil and polymethylpentene Expired EP0000697B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US817147 1977-07-20
US05/817,147 US4146487A (en) 1977-07-20 1977-07-20 Lubricating composition

Publications (2)

Publication Number Publication Date
EP0000697A1 EP0000697A1 (en) 1979-02-21
EP0000697B1 true EP0000697B1 (en) 1984-11-14

Family

ID=25222434

Family Applications (1)

Application Number Title Priority Date Filing Date
EP78100269A Expired EP0000697B1 (en) 1977-07-20 1978-06-29 A lubricating composition in the form of a gel consisting of an oil and polymethylpentene

Country Status (10)

Country Link
US (1) US4146487A (en)
EP (1) EP0000697B1 (en)
JP (1) JPS5422415A (en)
AU (1) AU515161B2 (en)
CA (1) CA1096367A (en)
DE (1) DE2830136A1 (en)
DK (1) DK153085C (en)
IT (1) IT1112280B (en)
NL (1) NL7806999A (en)
SE (1) SE442872B (en)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4239632A (en) * 1979-03-14 1980-12-16 Skf Industries, Inc. Lubricant composition
JPS55137198A (en) * 1979-04-13 1980-10-25 Ntn Toyo Bearing Co Ltd Lubricating composition for ball-and-roller bearing
US4534871A (en) * 1980-03-24 1985-08-13 Skf Industries, Inc. Lubricant insert for rolling bearings
EP0036692A1 (en) * 1980-03-24 1981-09-30 SKF Industrial Trading & Development Company B.V. Lubricant insert for rolling bearings
JPS57160595A (en) * 1981-03-31 1982-10-02 Nippon Radiator Co Ltd Manufacture of heat exchanger made of aluminum material
JPS5813930A (en) * 1981-07-20 1983-01-26 Matsushita Electric Ind Co Ltd Heating cooking device
US4492415A (en) * 1982-03-03 1985-01-08 Skf Industries, Inc. Unitary full complement bearing components containing rolling elements in a self-supporting lubricating matrix
US4915856A (en) * 1987-07-10 1990-04-10 Durafilm Corporation Solid lubricant composition
JP2846398B2 (en) * 1990-03-15 1999-01-13 古河電気工業株式会社 Method of manufacturing brazing sheet coil for vacuum brazing
US5415791A (en) * 1990-08-02 1995-05-16 Oiles Corporation Lubricating composition and a sliding member comprising the composition
JP2866457B2 (en) * 1990-08-02 1999-03-08 オイレス工業株式会社 Solid lubricant and sliding member embedded with the solid lubricant
JP3489586B2 (en) * 1991-10-25 2004-01-19 オイレス工業株式会社 Solid lubricant and sliding member embedded with the solid lubricant
US6228813B1 (en) 1993-04-30 2001-05-08 Nsk Ltd. Rolling bearing filled with a lubricant-containing polymer and process of the same
JPH07238940A (en) * 1994-02-28 1995-09-12 Ntn Corp Roller bearing
US5591808A (en) * 1994-10-03 1997-01-07 E/M Corporation Acetal-based self lubricating compositions
JP3925579B2 (en) 1998-02-03 2007-06-06 日本精工株式会社 Lubricant supply body, rolling bearing including the lubricant supply body, linear guide device, and ball screw device
US6062271A (en) * 1998-05-22 2000-05-16 Markel Corporation Polymethylpentene cable liner
JP2002212581A (en) * 2001-01-23 2002-07-31 Koyo Seiko Co Ltd Solid lubricating composition and polymer lubricant- sealed rolling bearing
US7683014B2 (en) * 2001-04-13 2010-03-23 Mitrovich Michael J Process for making a two-part solid lubricant stick
FR2913740B1 (en) * 2007-03-14 2009-09-04 Cie Engrenages Et Reducteurs M FLEXIBLE COUPLING DEVICE
FR2913742B1 (en) * 2007-03-14 2009-10-30 Cie Engrenages Et Reducteurs M CONNECTING SPRING FOR A FLEXIBLE COUPLING DEVICE
DE102007013934A1 (en) 2007-03-23 2008-09-25 Schaeffler Kg Transporting and mounting device for sets of rolling bodies arranged next to each has space between two adjacently arranged rolling bodies both inside and outside pitch circle filled with a material
DE102007041549A1 (en) 2007-08-31 2009-03-05 Schaeffler Kg roller bearing
US20140087980A1 (en) 2012-09-21 2014-03-27 Mpl Technology, Inc. Lubricant compositions
GB2551712A (en) * 2016-06-24 2018-01-03 Titus D O O Dekani Improvements in movement control devices
US10849192B2 (en) * 2017-04-26 2020-11-24 Agc Automotive Americas R&D, Inc. Enclosure assembly for window electrical connections

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT513721A (en) * 1953-01-27 1900-01-01
US3076764A (en) * 1960-09-30 1963-02-05 California Research Corp Isotactic polymers of 4-methyl-1-pentene as grease thickeners
US3541011A (en) * 1964-04-28 1970-11-17 Joseph E Ferri Lubricating composition
US3729415A (en) * 1964-04-28 1973-04-24 Ferri J Lubricating composition
US3547819A (en) * 1964-04-28 1970-12-15 Joseph E Ferri Lubricating composition
FR1604349A (en) * 1968-01-02 1971-10-11 Alkene polymer particles as thickening agents for ointments
JPS4833004A (en) * 1971-08-27 1973-05-07

Also Published As

Publication number Publication date
AU3745578A (en) 1980-01-03
US4146487A (en) 1979-03-27
SE442872B (en) 1986-02-03
DK153085B (en) 1988-06-13
CA1096367A (en) 1981-02-24
IT7825740A0 (en) 1978-07-17
DK322578A (en) 1979-01-21
JPS5625480B2 (en) 1981-06-12
JPS5422415A (en) 1979-02-20
AU515161B2 (en) 1981-03-19
EP0000697A1 (en) 1979-02-21
SE7807345L (en) 1979-01-21
IT1112280B (en) 1986-01-13
NL7806999A (en) 1979-01-23
DE2830136A1 (en) 1979-02-01
DK153085C (en) 1988-11-07

Similar Documents

Publication Publication Date Title
EP0000697B1 (en) A lubricating composition in the form of a gel consisting of an oil and polymethylpentene
US4239632A (en) Lubricant composition
US4357249A (en) Self-lubricating bearing and the like, and method of making same
US3541011A (en) Lubricating composition
US3729415A (en) Lubricating composition
US4041002A (en) Thermoplastic resin composition
JPS6014795B2 (en) Lithium complex grease and its manufacturing method
US2606153A (en) Silicone greases
JPH08170091A (en) Grease suitable for use at high temperature
US3194762A (en) Extreme pressure lubricant and method for making the same
US3247116A (en) Lubricants containing degraded polytetrafluoroethylene
US3432511A (en) Processing of plastic materials
CA1148926A (en) Lubricating composition
EP0395875A1 (en) Lubrication blends
US3839209A (en) Organometallic anti-friction compositions and their method of manufacture
GB2249811A (en) High temperature sliding bearing
US3852203A (en) Sliding bearing member
US2679480A (en) Indogen thickened grease composition
US4294712A (en) Self-lubricating bearing
US3630901A (en) Grease compositions
US3110669A (en) High temperature lubricants
JPH0575797B2 (en)
US2457582A (en) Grease composition
EP0108172B1 (en) Dimensionally stable structural members having a low coefficient of friction, and a composition and method of making them
JPH0762184A (en) Slidable sealing composition

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): BE CH FR GB LU

17P Request for examination filed
GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Designated state(s): BE CH FR GB LU

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: LU

Payment date: 19910508

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19910520

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19910523

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19910527

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19910530

Year of fee payment: 14

EPTA Lu: last paid annual fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19920629

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19920629

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Effective date: 19920630

Ref country code: CH

Effective date: 19920630

BERE Be: lapsed

Owner name: SKF INDUSTRIES INC.

Effective date: 19920630

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19920629

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19930226

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST