A plastics alloy for a bearing material comprising polyphenylene sulphide and polyether ether ketone. The alloy is formed by powder mixing, melt blending or solvent blending and applied to a metal backing either as a sheet, or in solution or in powder form. The alloy is heated and roll bonded to the backing.

Patent
   RE32595
Priority
Oct 22 1981
Filed
Feb 05 1986
Issued
Feb 09 1988
Expiry
Feb 05 2006
Assg.orig
Entity
Large
17
5
all paid
1. A method of making a plain bearing comprising a plastics alloy bearing layer and a metal backing, the method including the steps of mixing together a polyarylene sulphide and a polyether ketone to form an alloy, applying said alloy to said metal backing and bonding said alloy to said backing.
2. A method according to claim 1 wherein said alloy is formed by solvent blending.
3. A method according to claim 2 wherein said solvent is a benzyl benzoate.
4. A method according to claim 1 wherein said alloy is formed by melt blending.
5. A method according to any one of claims 1 or 4 wherein said alloy is applied to said backing as a sheet and roll bonded.
6. A method according to claim 1 wherein said alloy is formed by powder mixing.
7. A method according to any one of claims 1 or 4 or claim 6 wherein said alloy is applied to said backing in powder form and heated to bond it to said backing.
8. A plastics alloy comprising a polyarylene sulphide and an aromatic polyether ketone.
9. An alloy according to claim 8 wherein said polyarylene sulphide is polyphenylene sulphide.
10. An alloy as claimed in claim 9 in which the polyphenylene sulphide comprises from 20 to 50% by weight of the alloy.
11. An alloy according to any one of claims 8, 9 and 10 wherein said polyether ketone is polyether ether
ketone. 12. A laminated bearing comprising a metal backing member and a plastics alloy bearing member of a polyarylene sulphide and an aromatic polyether ketone bonded to said backing member. 13. A laminated bearing according to claim 12 wherein said polyarylene sulphide is polyphenylene sulphide. 14. A laminated bearing as claimed in claim 13 in which polyphenylene sulphide comprises from 20 to 50% by weight of the alloy forming the bearing member. 15. A laminated bearing according to any one of claims 12, 13 or 14 wherein said polyether ketone is polyether ether ketone. 16. A laminated bearing as claimed in claim 12 wherein the plastics alloy is one formed by solvent blending.
17. A laminated bearing as claimed in claim 16 wherein the solvent is benzyl benzoate. 18. A laminated bearing as claimed in claim 12 wherein the plastics alloy is one formed by powder mixing or melt blending.

The present invention relates to plastics alloy compositions for example for use as a bearing material, either as a lining or as an overlay. The invention is particularly concerned with lubricated plastics bearing materials.

Plastics bearing materials are known in themselves, however, some suffer from poor fatigue strength and so are unsuitable under certain conditions, while others suffer from overheating sometimes due to an inability to form an effective lubricant film.

It is an object of the present invention to provide a plastics bearing material which exhibits high fatigue strength and which does not suffer excessively from overheating.

According to the present invention, there is provided a plastics alloy, for example, for use as a bearing material, the alloy comprising a polyarylene sulphide and an aromatic polyether ketone.

The polyarylene sulphide is preferably polyphenylene sulphide and may be present in an amount of from 5 to 95% by weight, preferably, 20 to 50% by weight. The polyether ketone is preferably polyether ether ketone but may be a copolymer of an aromatic polyetherketone with an aromatic polysulphone or sulphide. Thus, the second polymeric component of the alloy is preferably a linear, semi-crystalline polymer containing the repeating units: ##STR1##

The morphology of the alloy can be semi-cyrstalline or amorphous, and it may be a single phase material or a fine dispersed polyphenylene sulphide phase in a matrix of the semi-crystalline second phase.

The alloy may be produced in a number of ways. One such way is solvent blending. In this method, hot solutions of the two polymers in the same solvent are mixed and the solvent is subsequently removed. This may be carried out by distillation or solvent extraction, thus leaving the polymer alloy. A preferred solvent is benzyl benzoate.

Another production method is melt blending. In this case the two polymers are melted and thoroughly mixed together in an internal mixing machine. Reactive additions (e.g. sulphur) can be made to promote some graft co-polymerisation by a free-radical mechanism between the component polymers to aid compatibility.

Free-radical initiating compounds can also be added to the mixed solutions in a solvent blending process. Such materials include those capable of producing thiyl free radicals, for example phenyl disulphide, ##STR2## in order to initiate some graft co-polymerisation between the component polymers and so enhance compatibility.

The alloy may be applied as an overlay by any known suitable method but is preferably applied by a solvent coating method. When used as an overlay, the alloy is preferably applied to an existing layer of bearing material.

When intended for use as a bearing lining, the alloy may be applied to a plain metal e.g. an aluminium alloy backing or a steel backing with an aluminium alloy bonding layer or a sintered (e.g. bronze) backing. The alloy may be applied in sheet form, as a powder or in solution.

When applied as a sheet, the polymer may be extruded and bonded to the backing simultaneously or may be extruded as a sheet and subsequently pressure bonded or roll bonded to a heated backing.

When used as a powder, either for direct application or for forming into a sheet, the alloy is preferably pre-dried,; when applied as a powder to a backing, the alloy may be spread on the backing using a vibrating feed hopper. The backing is preferably heated until the alloy melts and the alloy may then be roll bonded to the backing.

The alloy may be pressure bonded either as a sheet or when in powder form. In this method the backing may be formed into the desired shape and placed in a mould. The alloy is then placed on top of the backing, either as a sheet of the correct shape, or as a powder in the desired quantity, and subsequently pressure bonded. This method is particularly suitable for forming flat bearings such as thrust pads or washers.

When the alloy is applied in solution, this may be carried out by any suitable method, for example, dipping, spraying, roller coating or spreading.

Further components may be added to the two component alloys though preferably such an addition is a co-polymer of the two main components.

The alloy may be used for bearing bushes half-bearings, thrust pads, pads for journal bearings, slides for machine tools and marine stern bearings. The alloy may also be applicable generally to any two relatively sliding surfaces such as pistons operating in cylinders and most applications in internal combustion engines. The use of the alloy, however, is not intended to be limited to bearings.

The invention may be carried into practice in various ways and will now be illustrated in the following non-limiting examples.

Alloy compositions were made by solution blending PPS and PEEK using diphenyl sulphone as a mutual solvent with a small reactive addition of diphenyl disulphide. A glass reaction vessel equipped with a nitrogen inlet, a condenser column and a stirring device was charged with 500 grams of melted diphenyl sulphone and held at 300°C 100 grams of powdered PPS made as described in U.S. Pat. No. 3,919,177 of inherent viscosity of at least 0.20, and 100 grams of PEEK (ICI grade 45P) were slowly added while the mixture was stirred vigorously under a blanket of nitrogen. When all of the solid was in solution 2 grams of diphenyl disulphide powder was added and the temperature was raised to 320° C. for 15 minutes, then the mixture was cooled, the diphenyl sulphone was removed by washing with acetone (twice) the resulting solid was milled to pass a BS 44 mesh sieve then washed again with acetone (twice) and dried at 150°C under vacuum. The polymer alloy powder was fabricated into a test bearing lining in the following manner. The backing used was a 11/2 mm steel strip having a 5 micron copper plated overlayer and a porous layer of 11% tin/bronze (BS 60-100 mesh sieve) 1/2 mm thick sintered to the copper. The predried polymer powder was spread to a thickness of 11/2 mm by means of a vibrating feed hopper onto the substrate and then heated by induction heating to a temperature of between 360°C and 370°C The blank was rolled to consolidate the powder into a continuous coherent lining. The coated blank was then rapidly cooled and formed into a bearing.

Alloy compositions were prepared by melt extrusion of PPS and PEEK with small reactive additions of elemental sulphur and diphenyl disulphide. 5 kg. of PEEK (ICI grade 45P) and PPS powder (high molecular weight grade, of inherent viscosity at least 0.2 prepared as described in U.S. Pat. No. 3,919,177) were ball milled together with 100 grams of flowers of sulphur and 100 grams of diphenyl disulphide powder.

The mixture then was compounded together in the melt phase using a conventional melt extrusion apparatus. The resulting blend was extruded into the form of a strand which upon solidification was broken up into granules. The granules were then extruded again into continuous tape 15 cm wide 500 microns thick. The backing used was continuous copper plated steel strip with bronze powder sintered onto one side as described in Example 1. This backing strip was preheated to 360°C to 380°C by passing it through an induction heating coil, and with the polymer tape on top of it, passed into a rolling mill. The roll bonded strip was then rapidly water quenched and coiled. Bearing components were formed from the steel backed polymer alloy.

Davies, Glyndwr J.

Patent Priority Assignee Title
4835013, Feb 25 1987 Miba Sintermetall Aktiengesellschaft Process of manufacturing a substrate provided with a synthetic resin-bonded friction coating
5041335, May 02 1988 Sekisui Kagaku Kogyo Kabushiki Kaisha Undercoat composition and a metal substrate coated with a resin composition
5095078, Dec 16 1987 Kureha Kagaku Kogyo K. K. Heat-resistant film and production process thereof
5120808, Oct 25 1988 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
5139244, Sep 29 1989 BTR ANTIVIBRATION SYSTEMS, INC Slipper bushing assembly
5153264, Oct 25 1988 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
5153278, Oct 25 1988 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
5153279, Oct 25 1988 Kureha Kagaku Kogyo K.K. Poly(arylene thioether) block copolymer and production process thereof
5247052, Dec 31 1988 PEMEAS GmbH Fine-grained polyether-ketone powder, process for the manufacture thereof, and the use thereof
5328541, Dec 11 1991 Kureha Kagaku Kogyo Kabushiki Kaisha Method of welding tubular products of polyarylene sulfide and welded tubular structure
5395171, Sep 30 1992 The Torrington Company Polymer bearing housing
5433530, Sep 30 1992 The Torrington Company Polymer bearing housing
5998339, Jan 22 1997 Daido Metal Company Ltd. Wet type sliding apparatus comprising radial bearing
6012900, Sep 23 1998 Submergible pumping system with thermal sprayed polymeric wear surfaces
6565257, Sep 23 1998 Submergible pumping system with thermal sprayed polymeric wear surfaces
7001077, Nov 04 2003 Bearing or drive assembly with coated elements
D376160, Jun 29 1994 The Torrington Company Pillow block bearing housing
Patent Priority Assignee Title
2789957,
4017555, Jun 21 1976 FURON COMPANY, A CORP OF CA Polyalloy of polyphenylene sulfide and polyimide
4021596, Apr 22 1975 Phillips Petroleum Company Polyarylene sulfide resin alloys
4193645, Jun 13 1973 Glacier Metal Company, Limited Plain bearings
4386118, Jul 16 1975 Plastic bearing materials
///////
Executed onAssignorAssigneeConveyanceFrameReelDoc
Feb 05 1986AEPLC(assignment on the face of the patent)
Dec 18 1998A E PLC AN ENGLAND AND WALES CORPORATIONDana CorporationASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0111110362 pdf
Dec 18 1998A E PLC AN ENGLAND AND WALES CORPORATIONDANA CORPORATION A VIRGINIA COMMONWEALTH CORPORATIONCORRECTION OF DOCUMENT IDENTIFICATION NUMBER 101470113690938 pdf
Sep 01 2001Dana CorporationGIB HOLDINGS INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0126310492 pdf
Oct 26 2001GIB HOLDINGS INC GLACIER GARLOCK BEARINGS, INC ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0125810231 pdf
May 31 2002GLACIER GARLOCK BEARINGS, INC BANK OF AMERICA, N A , AS AGENTSECURITY AGREEMENT0132690866 pdf
Nov 04 2022BANK OF AMERICA, N A , AS AGENTGGB, INC F K A GLACIER GARLOCK BEARINGS INC , N K A GGB U S HOLDCO LLC TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS0618820313 pdf
Date Maintenance Fee Events
May 16 1991M174: Payment of Maintenance Fee, 8th Year, PL 97-247.
May 08 1995M185: Payment of Maintenance Fee, 12th Year, Large Entity.
Feb 01 1996ASPN: Payor Number Assigned.


Date Maintenance Schedule
Feb 09 19914 years fee payment window open
Aug 09 19916 months grace period start (w surcharge)
Feb 09 1992patent expiry (for year 4)
Feb 09 19942 years to revive unintentionally abandoned end. (for year 4)
Feb 09 19958 years fee payment window open
Aug 09 19956 months grace period start (w surcharge)
Feb 09 1996patent expiry (for year 8)
Feb 09 19982 years to revive unintentionally abandoned end. (for year 8)
Feb 09 199912 years fee payment window open
Aug 09 19996 months grace period start (w surcharge)
Feb 09 2000patent expiry (for year 12)
Feb 09 20022 years to revive unintentionally abandoned end. (for year 12)