Carbon-graphite/silicon carbide composite article

Information

  • Patent Grant
  • 5968653
  • Patent Number
    5,968,653
  • Date Filed
    Thursday, January 11, 1996
    28 years ago
  • Date Issued
    Tuesday, October 19, 1999
    24 years ago
Abstract
A carbon-graphite/silicon carbide composite article is provided. The composite article includes a carbon-graphite body intimately bonded to a dense silicon carbide body by a transition/bonding region which links the two bodies. The transition/bonding region between the carbon-graphite body and the silicon carbide body typically includes a layer rich in silicon metal and a small silicon carbide/silicon metal/carbon graphite area where some of the carbon-graphite from the carbon-graphite body has been converted to silicon carbide. The carbon-graphite body may also include a variety of impregnants.
Description

FIELD OF THE INVENTION
This invention relates to the field of carbon-graphite/silicon carbide composite articles and more particularly to composite articles comprised of carbon-graphite bodies bonded to silicon carbide bodies.
BACKGROUND OF THE INVENTION
In the area of friction and seal components for demanding applications, seal designs are often compromised by the need to choose among materials which have exclusive and independent benefits, and sometimes conflicting characteristics. The seal designs are often compromised in material selection because, while some materials have beneficial properties in certain respects, the materials may have disadvantages, or less desirable characteristics, in other respects. For example, some seal materials (i.e. carbon/graphites) have self-lubricating properties, and therefore perform very well in dry run and process upset conditions. Typically, such materials also have a low modulus of elasticity, which allows the materials to deflect against the mating face of a seal (which is usually a high modulus ceramic). However, because of the low modulus, such materials lack strength and stiffness. Further, the materials also lack high oxidation resistance.
Other seal materials (e.g. self-sintered silicon carbides) have superior strength and a high modulus of elasticity, which provides the stiffness necessary to give the entire seal assembly stability and strength, and have high oxidation resistance. However, such materials are not self-lubricating. Therefore, the materials have poor dry running and/or process upset response characteristics.
SUMMARY OF THE INVENTION
The present invention includes a carbon-graphite/silicon carbide composite article. The composite article includes a carbon-graphite body intimately bonded to a dense silicon carbide body by a transition/bonding region which links the two bodies. The transition/bonding region between the carbon-graphite body and the silicon carbide body typically includes a layer rich in silicon metal and a small silicon carbide/silicon metal/carbon graphite region where some of the carbon-graphite from the carbon-graphite body has been converted to silicon carbide. The carbon-graphite body, which typically would be used as a tribological material in a seal or bearing application, may also include a variety of impregnants to further enhance the tribological, physical or chemical characteristics of the body, or to eliminate the porosity of the body for seal applications.
In the production of the composite article of the present invention, the carbon-graphite body and the silicon carbide body are first manufactured separately. The two materials are then assembled and reacted to convert the silicon carbide body into a dense body and to produce the transition/bonding region which provides intimate adhesion between the previously separate bodies. Some overlap of part of the cross sections of the bodies is provided (i.e. so that one of the bodies is partially embedded in, or is keyed into, the other) to allow sufficient adhesion and shear strength to withstand application forces. The overlap may, for example, be provided by fitting part of one body into a race or groove formed in the other. After reaction of the bodies and formation of the composite article, the carbon-graphite body, which is porous, can then be impregnated with an impregnant to further enhance the tribological, physical or chemical characteristics of the body, or to eliminate the porosity of the body.
The resultant composite article of the present invention is a stiff, strong and self-lubricating article particularly suitable for seal and bearing members. The unique characteristics of the composite article combine the superior strength, high modulus of elasticity and high oxidation resistance of silicon carbide with the lower modulus and self-lubricating characteristics of mechanical carbon-graphite. Further, in seal applications, because the silicon carbide body is separated from the rubbing surface of the material by the carbon-graphite body, the running temperature of the composite article is reduced in both normal and adverse conditions from that of a plain, e.g. reaction bonded, silicon carbide body. Thus, the opportunity for thermal shock, as well as catastrophic failure of seal/bearing assemblies, is reduced.
Further, the resultant article of the present invention is unique in that it does not compromise the structure of the silicon carbide by introducing flaws, such as graphite inclusions, into the silicon carbide which would weaken the structure of the silicon carbide body and lower its modulus of elasticity and strength.





BRIEF DESCRIPTION OF THE DRAWINGS
The present invention will be more fully understood from the following detailed description considered in conjunction with the accompanying drawings, in which:
FIG. 1 is a detailed cross-sectional schematic representation of a carbon-graphite/silicon carbide composite article of the present invention;
FIGS. 2A, 2B, and 2C are photomicrographs, taken at 50.times., 100.times., and 400.times., respectively, of the composite article of FIG. 1;
FIG. 3 is a schematic illustration of the process for producing the composite article of FIG. 1.
FIG. 4A is an orthogonal top view of an exemplary composition of the composite article of FIG. 1; and
FIG. 4B is an orthogonal side sectional view of the composite article of FIG. 4A.





DETAILED DESCRIPTION
The present invention includes a carbon-graphite/silicon carbide composite article. In the preferred embodiment, the composite article comprises a dense silicon carbide body; two interstitial regions: (1) a dense layer rich in silicon metal and (2) a small silicon carbide/silicon metal/carbon-graphite layer; and a carbon-graphite body. The microstructure of the carbon-graphite body is porous and can be impregnated with a variety of impregnants to further enhance the tribological-physical-chemical characteristics of the carbon-graphite body, or to eliminate the porosity for seal applications.
As can best be seen in FIGS. 1 and 2A-C, in the preferred embodiment the composite article of the present invention comprises a carbon-graphite body 10 bonded to a dense silicon carbide body 12. A transition/bonding region 14 joins the carbon-graphite body 10 to the silicon-carbide body 12. The transition/bonding region 14 comprises a layer of silicon metal 16 and an area 18 which includes inclusions of silicon carbide 20, silicon metal 22, and carbon-graphite 24. The silicon carbide 20 results from conversion of carbon-graphite and silicon metal during the bonding process. The carbon-graphite body 10 may also include a variety of impregnants, such as resins/polymers, metals, glasses or other inorganic moieties or materials to improve the tribological or other characteristics of the body, or to eliminate porosity in the carbon-graphite body.
The process for producing the composite article of the present invention is shown schematically in FIG. 3. Manufacture of the composite article begins with separate production of the two individual bodies, the carbon-graphite body and the silicon carbide body, e.g. a reaction bonded silicon carbide body. The carbon-graphite body is manufactured in known manner by mixing fillers, such as carbons, graphites, inorganic additives and binders, having a particle size distribution that yields a moldable powder and a desired microstructure. The binders include coal tar pitch, petroleum pitch and/or resins. The mixture is then molded or compacted into a green body. After compaction, the green body is heated at an elevated temperature sufficient to carbonize the binder to yield a carbon-graphite body. The peak temperature must also be high enough to stabilize the body to minimize size changes during the subsequent bonding process. Any size change in the bonding process will cause deformation in the final product and possible weakening of the bond. The carbon-graphite body is then heat treated. The peak temperature can either be realized in the primary carbonization operation or in a subsequent heat treating process. Typically, the carbon-graphite body is then machined to produce a body with a desired size within allowable tolerances.
The silicon carbide body is manufactured in known manner. A reaction bonded silicon carbide body could, for example, be manufactured by mixing fillers (carbons, graphites, silicon carbide and temporary binders) having a particle size distribution that yields a moldable powder and desired microstructure. The body is then molded or compacted into a green body, which is then heated to carbonize the temporary binder to provide an intermediate strength to the body as well as to provide carbon for the subsequent bonding process. If necessary, the body can then be machined to a desired size within a desired tolerance.
The carbon-graphite body and the silicon carbide body are then assembled and reacted to intimately bond the carbon-graphite body to the silicon carbide body and to fully densify the silicon carbide body. The reaction process involves placing the assembled bodies onto a tray fitted with rails, together with elemental silicon metal which can rest between the rails, and heating the assembled bodies until the silicon becomes molten and wicks up the rails to infiltrate the assembly. While the silicon metal infiltrates the assembly, it reacts with the silicon carbide body. The metal also fills the interstitial space between the silicon carbide body and the carbon-graphite body and reacts slightly with the carbon-graphite body surface. This reaction forms a silicon carbide layer, with residual silicon metal existing between the bodies to bond them together after cooling.
Any silicon metal that wicks to the exterior of the carbon-graphite body can easily be removed later via machining. After removal of any such silicon carbide skin, the composite article may then be impregnated (using techniques common for porous carbon-graphite materials) either to eliminate the porosity in the carbon-graphite body or to improve the tribological or other characteristics of the body (or both). The composite body can then be further machined if necessary.
FIGS. 4A-B show an exemplary composite article in which a groove or race 28 has been machined in silicon carbide body 12 to accommodate carbon-graphite body 10. Carbon-graphite body 10 may be inserted into race 28 after both bodies 10 and 12 have been individually baked, heat treated, and machined as necessary. After assembly, bodies 10 and 12 may be reacted together and bonded with a layer of silicon metal as described above. As shown in FIGS. 2A-C and 4A-B, it is important that the carbon-graphite body and the silicon carbide body overlap in cross-section to ensure adequate bonding and bond shear strength.
The following examples illustrate the invention using a reaction bonded silicon carbide body. It would be clear to a person skilled in the art that a pressureless sintered silicon carbide body could be used in like manner, providing that the pressureless sintered silicon carbide has sufficient porosity to wick up silicon metal as described above.
EXAMPLE I
A composite article of the present invention as shown in FIGS. 4A-B was prepared from a reaction bonded silicon carbide body having the properties summarized in Table I (after being reacted) and a carbon-graphite body having the properties summarized in Table II (after being baked).
TABLE I______________________________________Apparent Density, gm/cm.sup.3 3.1 Flexural Strength, psi 40,000-4 pt. Compressive Strength, psi 400,000 Modulus of Elasticity, psi 56 .times. 10.sup.6 Porosity, % Volume 0.1 Permeability Nil Hardness, HK200 2300 Temperature Limit: Oxidizing Atmosphere, .degree. F. 2500 Neutral Atmosphere, .degree. F. 2500 Coefficient of Thermal Conductivity, 85 BTU/hr. ft.sup.2 - .degree. F./ft. (at 70.degree. F.) Coefficient of Thermal Expansion, 2.5 .mu.-in/in .degree. F. (70 to 1500.degree. F.)______________________________________
TABLE II______________________________________Apparent Density, gm/cm.sup.3 1.75 Flexural Strength, psi 9000 Hardness, Scleroscope 85 Specific Resistance, ohm/inch cube 0.0018 Ash, % Weight 8______________________________________
After reaction as described earlier, a composite article of the present invention was produced.
EXAMPLE II
Another example of a composite article of the present invention as shown in FIGS. 4A-B was produced from a body of the reaction-bonded silicon carbide described in Table I (after being reacted) and a carbon-graphite body having the properties summarized in Table III (after being baked).
TABLE III______________________________________Apparent Density, gm/cm.sup.3 1.76 Flexural Strength, psi 7000 Hardness, Scleroscope 71 Specific Resistance, ohm/inch cube 0.0012 Ash, % Weight 4.6______________________________________
EXAMPLE III
Another sample of a composite article of the present invention as shown in FIGS. 4A-B was prepared from a reaction-bonded silicon carbide body having the properties summarized in Table I (after being reacted) and a carbon-graphite body having the characteristics summarized in Table IV (after being baked).
TABLE IV______________________________________Apparent Density, gm/cm.sup.3 1.65 Flexural Strength, psi 5000 Hardness, Scleroscope 55 Specific Resistance, ohm/inch cube 0.0015 Ash, % Weight approx. 5______________________________________
The above description is not intended to limit the present invention. Alternative embodiments are possible. Accordingly, the scope of the invention should be determined by the appended claims and their legal equivalence, not by the embodiments described and shown above.
Claims
  • 1. A composite article comprising:
  • a. a first body comprising reaction bonded silicon carbide;
  • b. a second body of carbon-graphite; and
  • c. a transition region joining the first and second bodies, comprising a layer of silicon metal.
  • 2. A composite article according to claim 1 in which the transition region includes an area comprising inclusions of carbon-graphite, silicon metal, and silicon carbide.
  • 3. A composite article according to claim 1 in which the second body includes at least one impregnant.
  • 4. A composite article according to claim 1 in which the transition region further includes an area comprising inclusions of carbon-graphite and silicon carbide.
  • 5. A composite article according to claim 1 in which the second body includes at least one impregnant.
  • 6. A composite article according to claim 2 in which the second body includes at least one impregnant.
  • 7. A composite article according to claim 3 in which the second body includes at least one impregnant.
  • 8. A composite article consisting essentially of:
  • a. a first body of reaction bonded silicon carbide;
  • b. a second body of carbon-graphite; and
  • c. a transition region joining the first and second bodies comprising a layer comprising silicon metal and a layer comprising silicon carbide, silicon metal, and carbon graphite.
  • 9. A composite article consisting essentially of:
  • a. a first body of silicon carbide;
  • b. a second body of carbon-graphite;
  • c. a transition region joining the first and second bodies comprising a layer comprising silicon metal and a layer comprising silicon carbide, silicon metal, and carbon graphite; and
  • d. at least one inorganic impregnant.
  • 10. A composite article comprising a carbon-graphite body partially embedded in a silicon carbide body and adhered thereto by a transition layer comprising silicon metal.
  • 11. A composite article as claimed in claim 10 in which the transition layer further comprises a layer between the silicon metal and carbon-graphite, the layer being formed by reaction therebetween.
  • 12. A composite article comprising a silicon carbide body partially embedded in a carbon-graphite body and adhered thereto by a transition layer comprising silicon metal.
  • 13. A composite article as claimed in claim 12 in which the transition layer further comprises a layer between the silicon metal and carbon-graphite, the layer being formed by reaction therebetween.
  • 14. A composite article comprising:
  • a. a first body comprising silicon carbide;
  • b. a second body of carbon-graphite; .
  • c. a transition region joining the first and second bodies comprising a layer comprising silicon metal and a layer comprising silicon carbide, silicon metal, and carbon graphite.
  • 15. The composite article according to claim 14, wherein the silicon carbide of the first body is reaction bonded silicon carbide.
  • 16. The composite article according to claim 14, wherein the second body further comprises at least one impregnant.
  • 17. The composite article according to claim 14, wherein the transition region further comprises an area comprising inclusions of carbon-graphite and silicon carbide.
US Referenced Citations (109)
Number Name Date Kind
RE30286 Coppola et al. May 1980
2609318 Swentzel Sep 1952
2614946 Proudfoot Oct 1952
2614947 Heyroth Oct 1952
2636826 Nicholson Apr 1953
2691605 Hediger Oct 1954
2784112 Nicholson Mar 1957
2887393 Taylor May 1959
2897572 Hansen Aug 1959
2907972 Schildhauer et al. Oct 1959
2916460 Van Der Beck, Jr. Dec 1959
2938807 Anderson et al. May 1960
2941962 Van Der Bock, Jr. Jun 1960
3035325 Nicholson et al. May 1962
3051564 Dremming Aug 1962
3094679 O'Connor et al. Jun 1963
3108887 Lenie et al. Oct 1963
3166380 Kuhn Jan 1965
3175884 Kuhn Mar 1965
3189472 Taylor Jun 1965
3189477 Shaffer Jun 1965
3205043 Taylor Sep 1965
3252827 Rose et al. May 1966
3305372 Taylor Feb 1967
3372305 Mikulec Mar 1968
3459566 Wilson, Jr. et al. Aug 1969
3480395 McMullen et al. Nov 1969
3513019 Miller et al. May 1970
3520667 Taylor Jul 1970
3765300 Taylor et al. Oct 1973
3796564 Taylor et al. Mar 1974
3808012 Bailey et al. Apr 1974
3852099 Prochazka Dec 1974
3853566 Prochazka Dec 1974
3859399 Bailey et al. Jan 1975
3924034 Olcott Dec 1975
3925133 Olcott Dec 1975
3925577 Fatzer et al. Dec 1975
3954483 Prochazka May 1976
3960577 Prochazka Jun 1976
3968194 Prochazka Jul 1976
3969124 Stewart Jul 1976
3993602 Prochazka Nov 1976
4004934 Prochazka Jan 1977
4017319 Greskovich et al. Apr 1977
4023975 Prochazka May 1977
4031178 Johnson et al. Jun 1977
4041117 Prochazka Aug 1977
4080415 Coppola et al. Mar 1978
4081284 Prochazka et al. Mar 1978
4108929 Prochazka et al. Aug 1978
4109050 Mehan et al. Aug 1978
4119475 Prochazka et al. Oct 1978
4119689 Prochazka et al. Oct 1978
4119690 Prochazka et al. Oct 1978
4120731 Hillig et al. Oct 1978
4120827 Boos et al. Oct 1978
4122140 Greskovich et al. Oct 1978
4122155 Prochazka et al. Oct 1978
4123286 Coppola et al. Oct 1978
4124402 Greskovich et al. Nov 1978
4124403 Greskovich et al. Nov 1978
4124667 Coppola et al. Nov 1978
4135937 Murata et al. Jan 1979
4135938 Murata et al. Jan 1979
4141948 Laskow et al. Feb 1979
4144207 Ohnsorg Mar 1979
4148894 Hillig et al. Apr 1979
4150998 Morelock Apr 1979
4179299 Coppola et al. Dec 1979
4207226 Storm Jun 1980
4209474 Prochazka Jun 1980
4225356 Prochazka et al. Sep 1980
4233256 Ohnsorg Nov 1980
4237085 Smoak Dec 1980
4238433 Hillig et al. Dec 1980
4240835 Laskow et al. Dec 1980
4279656 Greskovich et al. Jul 1981
4294788 Laskow et al. Oct 1981
4312954 Coppola et al. Jan 1982
4327186 Murata et al. Apr 1982
4332755 Murata Jun 1982
4346049 Coppola et al. Aug 1982
4374792 Prochazka et al. Feb 1983
4379110 Greskovich et al. Apr 1983
4385020 Morelock May 1983
4419161 Hailey Dec 1983
4455385 Prochazka Jun 1984
4524138 Schwetz et al. Jun 1985
4525461 Boecker et al. Jun 1985
4530808 Renlund et al. Jul 1985
4551436 Johnson et al. Nov 1985
4551496 Renlund et al. Nov 1985
4554717 Vig et al. Nov 1985
4571414 Renlund et al. Feb 1986
4649022 Tischer et al. Mar 1987
4659002 Wallgren et al. Apr 1987
4666775 Kim et al. May 1987
4676940 Kim et al. Jun 1987
4690909 Okuno et al. Sep 1987
4692418 Boecker et al. Sep 1987
4693988 Boecker et al. Sep 1987
4701426 Okuno et al. Oct 1987
4908340 Frechette et al. Mar 1990
4932438 Kitmura et al. Jun 1990
5114886 Taukada May 1992
5135893 Dohi et al. Aug 1992
5422322 Chen et al. Jun 1995
5580834 Pfaff Dec 1996
Foreign Referenced Citations (27)
Number Date Country
0 145 496 Jun 1985 EPX
0 486 336 May 1992 EPX
0 500 447 Aug 1992 EPX
0 522 945 Jan 1993 EPX
22 34 924 Jan 1974 DEX
33 29 225 Feb 1984 DEX
62-82047 Apr 1987 JPX
62-138377 Jun 1987 JPX
62-132785 Jun 1987 JPX
63-011559 Jan 1988 JPX
63-9781 Jan 1988 JPX
63-26421 Feb 1988 JPX
63-92915 Apr 1988 JPX
63-163026 Jul 1988 JPX
63-186076 Aug 1988 JPX
63-260861 Oct 1988 JPX
63-265850 Nov 1988 JPX
64-37468 Feb 1989 JPX
11 72290 Jul 1989 JPX
21 50024 Jun 1990 JPX
21 92464 Jul 1990 JPX
22 55581 Oct 1990 JPX
365577 Mar 1991 JPX
32 15374 Sep 1991 JPX
32 15375 Sep 1991 JPX
WO 9418141 Aug 1994 WOX
WO 9523122 Aug 1995 WOX
Non-Patent Literature Citations (21)
Entry
Pure Industries, Inc., Pure Carbon Co., Brochure entitled "The Carbon Component Specialist".
Pure Industries, Inc., Pure Carbon Co., Brochure entitled "Rubbing Components for Mechanical Seals".
Pure Industries, Inc., Pure Carbon Co., Brochure entitled "Bearings for Difficult Applications".
Pure Industries, Inc., Pure Carbon Co., Brochure entitled "Purebide Components for Demanding Applications".
Investigation of Ceramics for High Temperature Turbine Vanes Final Report, Mar. 1972, by Svante Prochazka, prepared under Contract N00019-71-C-0290 for Department of Navy.
"Investigation of Ceramics for High Temperature Turbine Vanes" Final Report, Dec. 1972, by Svante Prochzka, prepared under Contract N00019-72-C-0129 for Department of Navy.
"Investigation of Ceramics for High Temperature Turbine Vanes"' Final Report, Mar. 20, 1973-Dec. 19, 1973, by Svante Prochazka & Peter C. Smith, prepared under Contract N62269-73-C-0356 for Department of Navy.
"Investigation of Ceramics for High Temperature Turbine Vanes"' Final Report, Jan. 23, 1974-Oct. 23, 1974, by Svante Prochazka et al., prepared under Contract N62269-74-C-0255 for Department of Navy.
Investigation of Ceramics for High Temperature Turbine Components-Final Report, Dec. 1975, by Svante Prochazka et al., prepared under Contract N62269-75-C-0122 for Department of Navy.
Investigation of Ceramics for High Temperature Turbine Components-Final Report, Mar. 25, 1976-Mar. 25, 1977, by Curtis A. Johnson et a., prepared under Contract N62269-76-C-0243 for Department of Navy.
"Substitution of Ceramics for Ductile Materials in Design" Report by J.A. Coppola et al., presented at National Symposium on "Ceramics in the Service of Man", Jun. 7, 1976.
"Beta Silicon Carbide" Report by Peter T. B. Shaffer, Materials Research Bulletin, vol. 4, pp. S97-S106, 1969, proceedings of Silicon Carbide International Conference, University Park, PA, Oct. 20-23, 1968.
"Problems in Silicon Carbide Device Development" Report by Peter T.B. Staffer, Materials Research Bulletin, vol. 4. pp. S13-S24, 1969, proceedings of Silicon Carbide International Conference, University Park, PA, Oct. 20-23, 1968.
"Phase Stability of Silicon Carbide in the Temary System Si-C-N" Report by A.R. Kieffer et al. Material Research Bulletin, vol. 4, pp. S153-S166, 1969, proceedings of Silicon Carbide International Conference, University Park, PA, Oct. 20-23, 1968.
"5.2.3 Silicon Carbide." pp. 5.2.3-1-.5.2.3-11.
Silicon Carbide-1973, edited by R.C. Marshall et al., pp. 343-402 420-426, University of Smith Carolina Press, 1974.
"Sintered Alpha Silicon Carbide Pump Bearings-Tribological Materials Optimization to Improve Reliability", by Heinrich Knoch, Joseph Kracker and William D. Long, Proceedings of the Tenth International Pump Users Symposium, Mar. 1993.
"Sintered Silicon Carbides with Controlled Porosity for Mechanical Face Seal Applications" by R. Divakar, STLE Lubrication, Journal of the Society of Tribologists and Lubrication Engineers, vol. 50, pp. 75-80, Presented at 48; Annual Meeting in Calgary, Alberta, Canada May 17-20, 1993.
Quarterly Progress Report No. 1, Report No. SRD-74-057, of contract N62269-74-C-0255, entitled "Investigation of Ceramics for High-Temperature Turbine Vanes," covering work performed from Jan. 25, 1974 to Apr. 23, 1974.
Semi-Annual Technical Report No. SRD-75-047 of contract N00014-74-C-0331, entitled "Ceramic Sintering," dated Apr. 1975.
Quarterly Progress Report No. 2, Report No. SRD-75-042, of contract N62269-75-C-0122, entitled "Investigation of Ceramics for High-Temperature Turbine Vanes," covering work performed from Jan. 19, 1975 to Apr. 18, 1975.