GB1589628A - Abradable materials and method for making such materials - Google Patents

Abradable materials and method for making such materials Download PDF

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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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General Electric Co
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General Electric Co
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Priority claimed from JP10863576A external-priority patent/JPS5334575A/en
Priority claimed from US05/748,931 external-priority patent/US4150998A/en
Application filed by General Electric Co filed Critical General Electric Co
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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)

**WARNING** start of CLMS field may overlap end of DESC **. 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
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.
GB47721/77A 1976-09-10 1977-11-16 Abradable materials and method for making such materials Expired GB1589628A (en)

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

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GB1589628A true GB1589628A (en) 1981-05-13

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GB (1) GB1589628A (en)

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PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19931116