US 5,043,303 AGrant
Filament-Containing Composite
Issue Date:1991-08-27
•44 Claims
Abstract
Boron nitride is coated on filaments of elemental carbon and/or silicon carbide, the coated filaments are contacted with an infiltration-promoting material containing elemental carbon to produce a preform wherein the filaments are substantially parallel and each filament is enveloped with infiltration-promoting material, and the preform is infiltrated with a molten solution of boron and silicon producing a composite containing boron nitride coated filaments.
Metadata
Assignee
- General Electric Company
Inventors
- Raj N. Singh
- William A. Morrison
Application Information
Application Number:US 216471&
Filing Date:1988-07-08
Priority Date:1987-09-28
Art Unit:224
Classifications
IPC:
C04G 3552
Field of Search:
50126442892;96;99;154;9060361;366;374;446;498;704
Patent Drawings
This patent does not have any drawings.
Description
Example 1
This example illustrates coating of the filaments with boron nitride.
Continuous silicon carbide filaments having a length of about 1.75 inches were placed on a molybdenum screen and coated with boron nitride by the following low pressure chemical vapor deposition process utilizing the reaction B.sub.3 N.sub.3 H.sub.3 Cl.sub.3 .fwdarw.3BN+3HCl.
The molybdenum screen containing the filaments was positioned at about the midpoint of the hot zone of a pyrex/quartz/pyrex furnace tube.
Commercial trichloroborazine (B.sub.3 N.sub.3 H.sub.3 Cl.sub.3) was used. A 1.00 gram sample of this solid was transferred in an argon-filled glove box to a pyrex end-section which contained a thermocouple vacuum gauge, a cold trap and a vacuum stopcock.
The closed pyrex end-section was then taken out of the glove box and attached to an end of the furnace tube and to a vacuum system. The end-section containing the trichloroborazine was then cooled using liquid nitrogen and the furnace tube was opened to the vacuum system via the stopcock of the pyrex end-section. After the system reached a pressure lower than 0.020 torr, the furnace was heated to about 1050.degree. C. When the pressure had again dropped below 0.020 torr and the furnace temperature had stabilized, the end-section containing the trichloroborazene was warmed by an oil bath maintained at 60.degree. C., whereupon the solid began to vaporize, depositing BN and liberating gaseous HCl in the hot zone of the furnace tube and producing an increase in pressure.
The pressure was observed to reach as high as about 200 torr before stabilizing at about 50 torr. After two hours, the pressure was found to have decreased to about 0.020 torr, whereupon the furnace was shut down and the system allowed to cool to room temperature before opening the tube and removing the sample.
Identification of the chemically vapor deposited layer as BN was accomplished by means of electrical resistance measurement and a quantitative ESCA analysis of a film deposited in substantially the same manner on a SiC disk surface. This film was amorphous to x-rays in the as-deposited condition and appeared fully dense and smooth at high magnification in the SEM.
Scanning electron microscopy observation of the ends of coated and broken filaments revealed that the coating was continuous and smooth and about 1.5 microns thick on the filament and left no significant portion of the filament exposed.
Example 2
The boron nitride-coated filaments produced in Example 1 were uniaxially aligned by placing them in a device for aligning filaments and maintaining the required spacing between them. This device was made from a copper foil laminated on a printed circuit board which was etched by the photolithographic technique in such a way as to produce parallel grooves about 0.006 inch diameter, 0.004 inch deep and 0.008 inch inch apart (center-to-center). The coated silicon carbide filaments were placed on this device and a simple scoop of the filaments using a straight edge led to filling of each of the grooves with a filament. This resulted in a single layer of uniformly spaced filaments which were lifted off the board by putting adhesive tapes across each end portion of the filament layer. The adhesive tapes were sufficient to maintain the alignment and spacing between the filaments. Several such pre-formed layers of filaments were produced in which the filaments were parallel and spaced about 100 microns from each other. A suspension comprised of 1 part (by weight) crushed carbon felt, 1 part of binder, and 1 part xylene was poured into a casting mold. Four layers of filaments were dropped into the mold, one at a time, and pushed toward the bottom of the mold with a straight edge. The house vacuum was then applied to the mold to produce a vacuum-cast preform containing coated filaments submerged in a slurry of crushed carbon fibers and binder. This preform was cured overnight in the mold at room temperature and subsequently for an hour at about 100.degree. C. At this point the preform had sufficient strength and could be shaped by machining. The crushed carbon in the preform provided the channels and optimum pore size for rapid infiltration of molten silicon by way of Si-C reaction and wicking. The preform was in the shape of a bar about 2.5 inches .times.0.5 inches .times.0.070 inches and had an open porosity of at least about 50% by volume.
The preform and solid pieces of infiltrant were placed on a woven carbon fabric which was contained in a BN-sprayed graphite tray. This tray was then placed in a carbon resistance heated belljar furnace and slowly heated at a rate of about 10.degree. C. per minute to about 400.degree. C. in a vacuum of about 0.05 torr. The slow heating at this stage assured slow decomposition of the epoxy binder which otherwise may lead to disintegration of the preform. Subsequent to this, the preform was rapidly heated to 1420.degree. C. at which point the infiltrant was fluid and reacted with the carbon cloth and got wicked into the preform. A considerable amount of heat which was detected by a thermocouple placed on top of the preform was generated due to the exothermic reaction of the infiltrant with carbon fibers in the matrix. The preform was held for 5 minutes under these conditions and then slowly cooled below the melting point of the infiltrant after which the furnace power was turned off and the infiltrated sample was cooled to room temperature in the vacuum of the belljar.
The resulting composite had a porosity of less than about 1% by volume. It was estimated to be comprised of, based on the volume of the composite, of about 70% by volume of silicon carbide phase and/or boron-containing silicon carbide phase formed in situ, about 10% by volume of a phase comprised of a solution of elemental boron and elemental silicon wherein boron was present in an amount of about 1.6% by weight of silicon, a minor amount of a compound of boron and silicon, and about 20% by volume of boron nitride coated filaments of silicon carbide of which the silicon carbide filament component comprised about 18% by volume.
The composite was broken in a three-point-bend flexure mode to determine the load-deflection behavior. The three-point-bend test results are illustrated in FIG. 1. From the graph in FIG. 1, it can be seen that this composite showed toughened-ceramic-like behavior. The load-deflection curve for this sample shows the onset of matrix cracking followed by a significant rise in the load carrying capability of the composite. An ultimate load was reached beyond which the composite showed graceful failure i.e., gradual decrease in the load on extensive failure of the composite.
A number of additional composites were prepared in substantially the same manner. The composites made in this way showed an ultimate strength between 45,000 psi and 72,000 psi.
Examination of the fractured cross-section in a Scanning Electron Microscope revealed fiber pullout which is consistent with the observed load-deflection behavior. Also, the boron nitride coating appeared intact around the filaments. All of the components of the composite were distributed through the composite. The filaments were substantially parallel to each other and there was no contact between filaments.
This composite would be useful as a high temperature structural material in an aircraft engine.
Example 3
This example was carried out in substantially the same manner as that disclosed in Example 2 except that the silicon carbide filaments were not coated with boron nitride.
The load-deflection behavior of this composite is shown in FIG. 1. From FIG. 1 it can be seen that this composite displayed brittle-ceramic-like behavior. The composite also showed a low strength (less than 30,000 psi).
Examination of the fractured cross-section in a Scanning Electron Microscope revealed no fiber pullout which is consistent with the observed load-deflection behavior.
Example 4
This example was carried out in substantially the same manner as disclosed in Example 3 except that no filaments were used.
The load-deflection behavior of this composite is shown in FIG. 1 and is the same as that produced by the composite of Example 3.
Claims
What is claimed is:
1. A process for producing a composite with a porosity of less than about 10% by volume comprised of boron nitride-coated filaments and a matrix phase, said filament component of said coated filaments comprising at least about 10% by volume of the composite, said matrix phase containing silicon carbide and/or boron-containing silicon carbide formed in situ in an amount of at least about 5% by volume of the composite and a solution of elemental boron and elemental silicon in an amount of at least about 1% by volume of the composite, which comprises the following steps: (a) providing a carbon-containing filament having a diameter of at least about 50 microns; (b) depositing a coating of boron nitride on said filament leaving no significant portion thereof exposed; (c) providing infiltration-promoting material in the form of particulates and/or fibers, said infiltration-promoting material containing elemental carbon; (d) contacting a plurality of said boron nitride-coated filaments with said infiltration-promoting material to produce a preform wherein said infiltration-promoting material envelops each coated filament preventing contact therebetween and wherein said coated filaments are at least substantially parallel to each other, said preform having an open porosity ranging from about 25% by volume to about 85% by volume of the preform; (e) providing an infiltrant comprised of boron and silicon containing elemental boron in solution in silicon in an amount of at least about 0.1% by weight of elemental silicon; (f) contacting said preform with infiltrant-associated infiltrating means whereby said infiltrant is infiltrated into said preform; (g) heating the resulting structure to a temperature at which said infiltrant is molten and infiltrating said molten infiltrant into said preform to produce an infiltrated product having the composition of said composite, said preform containing sufficient elemental carbon to react with said infiltrant to form said composite; and (h) cooling said product to produce said composite, said boron nitride-coated filaments being enveloped by said infiltration-promoting material to enable said infiltration by molten infiltrant.
2. The process according to claim 1 wherein said preform has an open porosity ranging from about 35% by volume to about 80% by volume.
3. The process according to claim 1 wherein said infiltration-promoting material is comprised of elemental carbon.
4. The process according to claim 1 wherein said filament is comprised of elemental carbon.
5. The process according to claim 1 wherein said filament is comprised of silicon carbide.
6. The process according to claim 1 wherein said matrix phase is comprised of said silicon carbide formed in situ and said elemental silicon.
7. The process according to claim 1 wherein said infiltration-promoting material is formed into a suspension in a liquid vehicle, wherein a layer of said boron nitride-coated filaments is pre-formed in which said filaments are spaced and substantially parallel, and wherein said layer of filaments is immersed in said suspension and said liquid vehicle is extracted therefrom to produce said preform.
8. The process according to claim 1 wherein said infiltration-promoting material is formed into a suspension, a part of said suspension is slip cast until a pliable mass of said infiltration-promoting material is formed, said boron nitride-coated filaments are pressed into said mass and additional suspension is slip cast on at least the exposed portions of said filaments to produce said preform.
9. A composite comprised of boron nitride-coated carbon-containing filaments and a matrix phase, said matrix phase containing silicon carbide phase and/or boron-containing silicon carbide phase and a solution phase comprised of a solution of boron and silicon wherein boron is present in an amount of at least about 0.1% by weight of silicon, said carbide phase being present in an amount of at least about 5% by volume of said composite, said solution phase being present in an amount of at least about 1% by volume of said composite, said filament component of said boron nitride-coated filaments being present in an amount of at least about 10% by volume of said composite, said boron nitride coating being at least detectable by scanning electron microscopy, said boron nitride-coated filaments being at least substantially parallel to each other and spaced from each other, said filament component of said boron nitride-coated filaments having a diameter of at least about 50 microns, said boron nitride-coated filaments being spaced from each other by at least about 50 microns, said matrix phase being continuous, interconnecting and enveloping each of said boron nitride-coated filaments, said composite having a porosity of less than about 10% by volume.
10. The composite according to claim 9 wherein a compound of boron and silicon is present ranging up to about 10% by volume of said composite.
11. The composite according to claim 9 wherein said filament component is comprised of elemental carbon.
12. The composite according to claim 9 wherein said filament component is comprised of silicon carbide.
13. The composite according to claim 9 wherein said matrix phase is comprised of said silicon carbide phase and said solution phase.
14. The composite according to claim 9 wherein said filament component is present in an amount of at least about 50% by volume of said composite.
15. A composite comprised of at least a layer of boron nitride-coated filaments and a matrix phase, said filament component of said boron nitride-coated filaments ranging from about 10% by volume to about 70% by volume of the composite and being selected from the group consisting of elemental carbon, a SiC-containing material containing by weight of the SiC-containing material at least about 50% by weight of silicon and at least about 25% by weight of carbon, and a combination thereof, said boron nitride coating being at least detectable by scanning electron microscopy, said boron nitride-coated filaments being at least substantially parallel to each other and spaced from each other, said filament component of said boron nitride-coated filaments having a diameter of at least about 50 microns, said boron nitride-coated filaments being spaced from each other by at least about 50 microns, said matrix phase being continuous, interconnecting and enveloping each of said boron nitride-coated filaments, said coated filaments being distributed through said composite, said matrix phase being comprised of a phase of silicon carbide and/or boron-containing silicon carbide and a solution phase, said solution phase being comprised of a solution of boron and silicon wherein boron is present in an amount of at least about 1% by weight of silicon, said carbide phase being present in an amount of at least about 10% by volume of said composite, said solution phase being present in an amount of at least about 1% by volume of said composite, said matrix phase enveloping each of said boron nitride-coated filaments, said composite having a porosity of less than about 10% by volume.
16. The composite according to claim 15 wherein a compound of boron and silicon is present ranging up to about 10% by volume of said composite.
17. The composite according to claim 15 wherein said silicon carbide phase ranges from about 10% by volume to less than about 79% by volume of said composite.
18. The composite according to claim 15 wherein said filament component is comprised of elemental carbon.
19. The composite according to claim 15 wherein said filament component is comprised of silicon carbide.
20. The process according to claim 1, wherein said infiltration-promoting material in step (c) contains molybdenum in an amount of at least about 1% by volume of said infiltration-promoting material.
21. The composite according to claim 9, wherein said matrix phase contains molybdenum silicide ranging up to about 50% by volume of the composite.
22. The composite according to claim 15, wherein said matrix phase contains molybdenum silicide ranging up to about 50% by volume of the composite.
23. A composite comprised of boron nitride-coated carbon-containing filaments and a matrix phase, said matrix phase containing silicon carbide phase and/or boron-containing silicon carbide phase and a solution phase comprised of a solution of boron and silicon wherein boron is present in an amount of at least about 0.1% by weight of silicon, said carbide phase being present in an amount of at least about 5% by volume of said composite, said solution phase being present in an amount of at least about 1% by volume of said composite, said filament component of said boron nitride-coated filaments being present in an amount of at least about 10% by volume of said composite, said boron nitride coating being at least detectable by scanning electron microscopy, said boron nitride-coated filaments being at least substantially parallel to each other and spaced from each other, said filament component of said boron nitride-coated filaments having a diameter of at least about 50 microns, said matrix phase being continuous, interconnecting and enveloping each of said boron nitride-coated filaments, said composite having a porosity of less than about 10% by volume.
24. The composite according to claim 23, wherein said filament component is comprised of elemental carbon.
25. The composite according to claim 23, wherein said filament component is comprised of silicon carbide.
26. The composite according to claim 23, wherein said matrix phase contains molybdenum silicide ranging up to about 50% by volume of the composite.
27. A process for producing a composite with a porosity of less than about 10% by volume comprised of boron nitride-coated filaments and a matrix phase, said filament component of said coated filaments comprising at least about 10% by volume of the composite, said matrix phase containing silicon carbide and/or boron-containing silicon carbide formed in situ in an amount of at least about 5% by volume of the composite and a solution of elemental boron and elemental silicon in an amount of at least about 1% by volume of the composite, which comprises the following steps: (a) providing a carbon-containing filament having a diameter of at least about 50 microns; (b) depositing a coating of boron nitride on said filament leaving no significant portion thereof exposed; (c) providing infiltration-promoting material in the form of particulates and/or fibers, said infiltration-promoting material containing elemental carbon; (d) contacting a plurality of said boron nitride-coated filaments with said infiltration-promoting material to produce a preform wherein said infiltration-promoting material envelops each coated filament preventing contact therebetween and wherein said coated filaments are at least substantially parallel to each other, said preform having an open porosity ranging from about 25% by volume to about 85% by volume of the preform; (e) providing an infiltrant composition comprised of boron and silicon wherein boron ranges from about 0.1% by weight to about 10% by weight of elemental silicon; (f) contacting said preform and said infiltrant composition with infiltrating means whereby molten infiltrant is infiltrated into said preform; (g) heating the resulting structure to a temperature at which said infiltrant composition is molten resulting in a molten infiltrant containing elemental boron in solution in silicon in an amount ranging from about 0.1% by weight of silicon to an amount which forms a saturated solution with silicon and infiltrating said molten infiltrant into said preform to produce an infiltrated product having the composition of said composite, said preform containing sufficient elemental carbon to react with said infiltrant to form said composite; and (h) cooling said product to produce said composite, said boron nitride-coated filaments being enveloped by said infiltration-promoting material to enable said infiltration by molten infiltrant.
28. The process according to claim 27, wherein said filament is comprised of elemental carbon.
29. The process according to claim 27, wherein said filament is comprised of silicon carbide.
30. The process according to claim 27, wherein said infiltration-promoting material in step (c) contains molybdenum in an amount of at least about 1% by volume of said infiltration-promoting material.
31. A process for producing a composite with a porosity of less than about 10% by volume comprised of boron nitride-coated filaments and a matrix phase, said filament component of said coated filaments comprising at least about 10% by volume of the composite, said matrix phase containing silicon carbide and/or boron-containing silicon carbide formed in situ in an amount of at least about 5% by volume of the composite and a solution of elemental boron and elemental silicon in an amount of at least about 1% by volume of the composite, which comprises the following steps: (a) providing a carbon-containing filament having a diameter of at least about 50 microns; (b) depositing a coating of boron nitride on said filament leaving no significant portion thereof exposed; (c) forming a preform comprised of infiltration-promoting material and a plurality of said boron nitride-coated filaments wherein said infiltration-promoting material envelops each coated filament preventing contact therebetween and wherein said coated filaments are at least substantially parallel to each other, said preform having an open porosity ranging from about 25% by volume to about 85% by volume of the preform, said infiltration-promoting material being in the form of particulates and/or fibers, said infiltration-promoting material containing elemental carbon; (d) providing an infiltrant comprised of boron and silicon containing elemental boron in solution in silicon in an amount of at least about 0.1% by weight of elemental silicon; (e) contacting said preform with infiltrant-associated infiltrating means whereby said infiltrant is infiltrated into said preform; (f) heating the resulting structure to a temperature at which said infiltrant is molten and infiltrating said molten infiltrant into said preform to produce an infiltrated product having the composition of said composite, said preform containing sufficient elemental carbon to react with said infiltrant to form said composite; and (g) cooling said product to produce said composite, said boron nitride-coated filaments being enveloped by said infiltration-promoting material to enable said infiltration by molten infiltrant.
32. The process according to claim 31, wherein said preform has an open porosity ranging from about 35% by volume to about 80% by volume.
33. The process according to claim 31, wherein said infiltration-promoting material in step (c) is comprised of elemental carbon.
34. The process according to claim 31, wherein said filament is comprised of elemental carbon.
35. The process according to claim 31, wherein said filament is comprised of silicon carbide.
36. The process according to claim 31, wherein said infiltration-promoting material in step (c) contains molybdenum in an amount of at least about 1% by volume of said infiltration-promoting material.
37. A process for producing a composite with a porosity of less than about 10% by volume comprised of boron nitride-coated filaments and a matrix phase, said filament component of said coated filaments comprising at least about 10% by volume of the composite, said matrix phase containing silicon carbide and/or boron-containing silicon carbide formed in situ in an amount of at least about 5% by volume of the composite and a solution of elemental boron and elemental silicon in an amount of at least about 1% by volume of the composite, which comprises the following steps: (a) providing a carbon-containing filament having a diameter of at least about 50 microns; (b) depositing a coating of boron nitride on said filament leaving no significant portion thereof exposed; (c) forming a preform comprised of infiltration-promoting material and a plurality of said boron nitride-coated filaments wherein said infiltration-promoting material envelops each coated filament preventing contact therebetween and wherein said coated filaments are at least substantially parallel to each other, said preform having an open porosity ranging from about 25% by volume to about 85% by volume of the preform, said infiltration-promoting material being in the form of particulates and/or fibers, said infiltration-promoting material containing elemental carbon; (d) providing an infiltrant composition comprised of boron and silicon wherein boron ranges from about 0.1% by weight to about 10% by weight of elemental silicon; (e) contacting said preform and said infiltrant composition with infiltrating means whereby molten infiltrant is infiltrated into said preform; (f) heating the resulting structure to a temperature at which said infiltrant composition is molten resulting in a molten infiltrant containing elemental boron in solution in silicon in an amount ranging from about 0.1% by weight of silicon to an amount which forms a saturated solution with silicon and infiltrating said molten infiltrant into said preform to produce an infiltrated produce having the composition of said composite, said preform containing sufficient elemental carbon to react with said infiltrant to form said composite; and (g) cooling said product to produce said composite, said boron nitride-coated filaments being enveloped by said infiltration-promoting material to enable said infiltration by molten infiltrant.
38. The process according to claim 37, wherein said filament is comprised of elemental carbon.
39. The process according to claim 37, wherein said filament is comprised of silicon carbide.
40. The process according to claim 37, wherein said infiltration-promoting material in step (c) contains molybdenum in an amount of at least about 1% by volume of said infiltration-promoting material.
41. The process according to claim 1, wherein said infiltration-promoting material in step (c) contains molybdenum carbide in an amount of at least about 1% by volume of said infiltration-promoting material.
42. The process according to claim 27, wherein said infiltration-promoting material in step (c) contains molybdenum carbide in an amount of at least about 1% by volume of said infiltration-promoting material.
43. The composite according to claim 9, wherein said matrix phase contains molybdenum carbide ranging up to about 50% by volume of the composite.
44. The composite according to claim 23, wherein said matrix phase contains molybdenum carbide ranging up to about 50% by volume of the composite.