GB1589628A - Abradable materials and method for making such materials - Google Patents
Abradable materials and method for making such materials Download PDFInfo
- Publication number
- GB1589628A GB1589628A GB47721/77A GB4772177A GB1589628A GB 1589628 A GB1589628 A GB 1589628A GB 47721/77 A GB47721/77 A GB 47721/77A GB 4772177 A GB4772177 A GB 4772177A GB 1589628 A GB1589628 A GB 1589628A
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- preform
- mold
- blend
- weight
- rotary
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/565—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide
- C04B35/573—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide obtained by reaction sintering or recrystallisation
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/62204—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products using waste materials or refuse
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/71—Ceramic products containing macroscopic reinforcing agents
- C04B35/78—Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
- C04B35/80—Fibres, filaments, whiskers, platelets, or the like
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- C04B37/00—Joining burned ceramic articles with other burned ceramic articles or other articles by heating
- C04B37/003—Joining burned ceramic articles with other burned ceramic articles or other articles by heating by means of an interlayer consisting of a combination of materials selected from glass, or ceramic material with metals, metal oxides or metal salts
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
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- G—PHYSICS
- G04—HOROLOGY
- G04G—ELECTRONIC TIME-PIECES
- G04G15/00—Time-pieces comprising means to be operated at preselected times or after preselected time intervals
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- G—PHYSICS
- G04—HOROLOGY
- G04G—ELECTRONIC TIME-PIECES
- G04G5/00—Setting, i.e. correcting or changing, the time-indication
- G04G5/02—Setting, i.e. correcting or changing, the time-indication by temporarily changing the number of pulses per unit time, e.g. quick-feed method
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/42—Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
- C04B2235/422—Carbon
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- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/42—Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
- C04B2235/428—Silicon
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- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/5216—Inorganic
- C04B2235/524—Non-oxidic, e.g. borides, carbides, silicides or nitrides
- C04B2235/5248—Carbon, e.g. graphite
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- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5296—Constituents or additives characterised by their shapes with a defined aspect ratio, e.g. indicating sphericity
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- C04B2235/5427—Particle size related information expressed by the size of the particles or aggregates thereof millimeter or submillimeter sized, i.e. larger than 0,1 mm
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- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
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- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5436—Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/658—Atmosphere during thermal treatment
- C04B2235/6581—Total pressure below 1 atmosphere, e.g. vacuum
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- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
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- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/02—Aspects relating to interlayers, e.g. used to join ceramic articles with other articles by heating
- C04B2237/16—Silicon interlayers
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- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
- C04B2237/32—Ceramic
- C04B2237/36—Non-oxidic
- C04B2237/365—Silicon carbide
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- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
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- C04B2237/61—Joining two substrates of which at least one is porous by infiltrating the porous substrate with a liquid, such as a molten metal, causing bonding of the two substrates, e.g. joining two porous carbon substrates by infiltrating with molten silicon
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Description
(54) IMPROVEMENTS IN ABRADABLE MATERIALS AND
METHOD FOR MAKING SUCH MATERIALS
(71) We, GENERAL ELECTRIC
COMPANY, a corporation organized and existing under the laws of the State of New
York, United States of America, of 1 River
Road, Schenectady 12305, State of New York,
United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: The present invention relates to a method for making abradable material useful as rotary sealant in turbine buckets and aircraft engines.
More particularly, the present invention relates to a method of making rotary sealant by heating a shaped blend of carbon fibre and silicon powder under reduced pressure to a temperature sufficient to convert the silicon powder to the molten state.
Prior to the present invention, rotary seals used in various parts of power producing apparatus, such as gas turbines, were made by various procedures, such as shown by Butts
U.S. patent 3,383,207 and Daunt U.S. patent 3,547,445. An abradable material was used to provide a seal between a rotating member and a stationary member to inhibit fluid flow between such members. Some of the abradable materials were based on the use of an epoxy resin and certain hollow organic particles having a bulk density of 3-5 pounds per cubic foot and an outside diameter of up to 0.02 inch. Other types of abradable materials are shown by the aforementioned U.S. patent of
Butts, based on the use of a plurality of hollow substantially spherical powder particles and more particularly the use of substantially spherical coated aluminum powder.
In our Patent Application No. 3805/77 (Serial No. 1,556,881) certain machinable castings are described and a method for making such materials. The castings can be employed as contiguous layers on shaped ceramic substrates, such as silicon carbide-silicon composites which may be in the form of a gas turbine shroud section. As described therein the aforementioned contiguous layers or composites having such contiguous layer integrally bonded to a ceramic base can be made by the infiltration of molten silicon into a mold containing a uniform mixture of particulated carbon and a particulated inorganic material, such as boron nitride, which can be in contact with either a shaped mass of silicon carbide or a composite of silicon and silicon carbide or a carbon fibre preform. Although the aforementioned procedure in our cop enduing application provides for valuable machinable castings or composites consisting of a ceramic base and an abradable surface layer, it requires the incorporation of a shaped part to mold and the infiltration of molten silicon from the outside into the mold to provide for the in situ formation of the machinable casting or composite having the machinable casting as an abradable layer. As a result, the resulting molten silicon infiltration reaction product contains nibs which must be machined off before the finished part can be used. It would be desirable therefore to produce an abradable material which can be used as rotary sealant to prevent fluids at different pressures from mixing in a gas turbine engine and aircraft engine applications without requiring molten silicon infiltration into a confined cavity resulting in the production of shaped reaction products requiring machining.
The present invention is based on the discovery that blends of silicon powder and carbon fibre containing up to 10% by weight of a binder can be shaped under heat and pressure to produce a preform and thereafter molded at temperatures of up to 1600 C, preferably in non-oxidising atmosphere, and under reduced pressure to produce abradable rotary seals useful in a variety of applications.
There is provided by the present invention, a method for making a shaped abradable mass useful as a rotary sealant comprising
(1) mixing together from 60% to 80% by weight of silicon powder having an average particle size in the range of from 25 microns to 200 microns, with 20% to 40% by weight of carbon fibre having a length to diameter ratio with average value of from 1 to 20 and with from 5% to 20% by weight of organic binder,
(2) shaping the mixture of (1) at a temperature of up to 100"C and a pressure of up to 3000 psig to produce a preform and
(3) molding the preform of (2) under reduced pressure at a temperature of up to 1600 C.
Included by the organic resin binders which can be used in the practice of the method of the present invention to produce the rotary seals are, for example, epoxy resin, paraffin wax, acrylic ester resins, polystyrenes, etc.
Included by the carbon fibers which can be employed in the practice of the present invention are, for example, crushed WDF graphite felt and crushed WCA graphite cloth, manufactured by Union Carbide Corporation.
In the practice of the invention the abradable sealant compositions can be made by initially blending together the silicon powder, the carbon fiber and the binder. The dry blend can then be processed to activate the binder before it is converted to the preform. The preform can then be placed in a mold treated with a release agent and designed to accommodate the preform. The preform can then be heated under reduced pressure while in the mold to a temperature sufficient to convert the powdered silicon to the molten state to provide for in situ interaction between the carbon fiber and the molten silicon, preferably in a substantially non-oxidizing atmosphere.
Depending upon the nature of the binder employed in the blend of silicon powder and carbon fiber, the formation of the preform can vary. Experience has shown that in most instances the preform can be made by placing the blend in a mold and pressing it to the desired shape. Accordingly, the mold cavity used to make the preform is generally the same shape as the mold cavity used to produce the final machinable shaped rotary sealant material.
A suitable release agent which can be used to treat the inside surface of the mold employed to convert the preform to the machinable rotary sealant material is boron nitride.
It has been found that the preform can be con verted to the machinable rotary sealant material in as little as 5 minutes or less to as long as 30 minutes or more, depending upon the rate which the mold is heated. Temperatures in the range of from 1500"C to 1600 C can be used. Effective results can be achieved at reduced pressures of from .01 torr to 2000 torr and preferably from 1 to 100 torr.
Depending upon the composition of the preform the resulting machinable rotary sealant can have a density in the range of from 1 to 2.
In most instances, optimum abradable characteristics can be achieved while providing satisfactory sealant properties if the density of the rotary sealant is in the range of from 1.1 to 1.3 based on the use of an initial blend having from 72 to 70 percent by weight silicon powder and 28 to 30 percent by weight of carbon fiber.
In order that those skilled in the art will be better able to practise the invention, the following examples are given by way of illustration and not by way limitation. All parts are by weight.
Example 1.
A blend of 0.5 part of WDF felt, a product of the Union Carbide Corporation, which had been crushed at 3000 psi, 1 part of 80 mesh powder silicon and 0.1 part paraffin wax was mixed dry then heated to 100"C for 10 minutes and mixed again. A preform was made by placing the blend in a mold having a 7/8 in.
X 1/8 in. cavity and pressed to 3000 psi. The resulting disc was then placed in a boron nitride treated mold having a cavity approximately 7/8 in. X 1/8 in. The preform was heated to a temperature of 1500 C for 20 minutes while it was maintained at a pressure of 0.5 torr.
The mold was then allowed to cool and the 7/8 in. X 1/8 in. disc was removed from the mold. The disc was found to be rigid and porous and easily cut with a hack saw blade.
Example 2.
A blend of 1.8 WCA cloth, a product of the
Union Carbide Corporation, which had been crushed at 15,000 psi, 4.7 parts of 200 mesh silicon powder and 6 part epoxy resin was mixed. A preform was made by placing the blend in a mold having a 1.5 in. X 1.7 in.
X .125 in. cavity and pressed to 3000 psi at 100"C for 30 minutes. The resulting sheet was removed from the mold and then placed on a previously machined SiC rotary seal backing with .1 part epoxy resin used to fix the preform to the SiC surface. This assembly was then placed in a boron nitride treated mold and blended to a temperature of 15500C for 20 minutes while it was maintained at a pressure of 100 torr.
The mold was then allowed to cool and the
SiC backing with the 1.5 in. X 1.7 in. X 125 in. sheet attached was removed from the mold. The sheet was found to be rigid, firmly attached to the SiC backing with a Si bond, porous and easily cut with a hack saw blade.
WHAT WE CLAIM IS: - 1. A method for making a shaped abradable mass useful as a rotary sealant comprising
1) mixing together from 60% to 80% by
weight of silicon powder having an average
particle size in the range of from 25 microns
to 200 microns with 20% to 40% by weight
of carbon fibre having a length to diameter
ratio with average value of from 1 to 20
and with from 5% to 20% by weight of an
organic binder,
2) shaping the mixture of (1) at a tem
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (6)
1. A method for making a shaped abradable mass useful as a rotary sealant comprising
1) mixing together from 60% to 80% by
weight of silicon powder having an average
particle size in the range of from 25 microns
to 200 microns with 20% to 40% by weight
of carbon fibre having a length to diameter
ratio with average value of from 1 to 20
and with from 5% to 20% by weight of an
organic binder,
2) shaping the mixture of (1) at a tem
perature of up to 100"C and a pressure of
up to 3000 psig to produce a preform and
3) moulding the preform of (2) under re
duced pressure at a temperature of up to 16000 C.
2. A method in accordance with Claim 1, where the binder is paraffin wax.
3. A method in accordance with Claim 1 or
Claim 2 where the carbon fibre is obtained from a carbon felt cloth.
4. A method according to any one of Claims 1 to 3 in which the Si-C mixture is a blend of 70 to 72',t, Si and 28 to 30t,', C.
5. A method according to Claim 1 and substantially as herein described with reference to any one of the examples.
6. A rotary sealant when produced by a method as claimed in any one of the Claims 1 to 5.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10863576A JPS5334575A (en) | 1976-09-10 | 1976-09-10 | Time adjusting device for electronic clock |
US05/748,931 US4150998A (en) | 1976-12-09 | 1976-12-09 | Rotary sealant abradable material and method for making |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1589628A true GB1589628A (en) | 1981-05-13 |
Family
ID=26448467
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB47721/77A Expired GB1589628A (en) | 1976-09-10 | 1977-11-16 | Abradable materials and method for making such materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1589628A (en) |
-
1977
- 1977-11-16 GB GB47721/77A patent/GB1589628A/en not_active Expired
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PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19931116 |