US3427185A - Composite structural material incorporating metallic filaments in a matrix,and method of manufacture - Google Patents
Composite structural material incorporating metallic filaments in a matrix,and method of manufacture Download PDFInfo
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- US3427185A US3427185A US346388A US3427185DA US3427185A US 3427185 A US3427185 A US 3427185A US 346388 A US346388 A US 346388A US 3427185D A US3427185D A US 3427185DA US 3427185 A US3427185 A US 3427185A
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- matrix
- mat
- filamentary
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- composite structural
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Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/08—Metallic material containing only metal elements
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- 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
- C04B35/74—Ceramic products containing macroscopic reinforcing agents containing shaped metallic materials
- C04B35/76—Fibres, filaments, whiskers, platelets, or the like
-
- 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
- C22C47/16—Making alloys containing metallic or non-metallic fibres or filaments by thermal spraying of the metal, e.g. plasma spraying
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/137—Spraying in vacuum or in an inert atmosphere
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/902—High modulus filament or fiber
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/934—Electrical process
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9335—Product by special process
- Y10S428/937—Sprayed metal
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49801—Shaping fiber or fibered material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12014—All metal or with adjacent metals having metal particles
- Y10T428/1216—Continuous interengaged phases of plural metals, or oriented fiber containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12444—Embodying fibers interengaged or between layers [e.g., paper, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/10—Scrim [e.g., open net or mesh, gauze, loose or open weave or knit, etc.]
- Y10T442/102—Woven scrim
- Y10T442/109—Metal or metal-coated fiber-containing scrim
Definitions
- This invention relates to composite structural materials, and more particularly to an improved composite structural material incorporating metallic filaments in a matrix, which is characterized by a high strength-to-weight ratio and resistance to deterioration in high-temperature atmosphere, and a novel method of manufacture thereof.
- the present application is a continuation-in-part of our copending application S.N. 93,941, filed Mar. 7, 1961, now abandoned.
- the tensile strength of whisker crystals may approximate the atomic cohesion strength of the metal; in the case of iron whiskers, strengths of 1,900,000 p.s.i. have been shown, and in the case of copper crystals, 430,000 p.s.i., each exceeding the tensile strength of large sections of the same metals by a factor of more than ten. The reason for this great strength is not clearly understood, but may be based upon the low incidence of edge dislocations which can exist within the small diameter of whiskers.
- fine metallic filamentary materials in the form of fine wires or whisker crystals may be embedded in a coalescent matrix of further material to form a composite material which exhibits improved characteristics.
- the tensile strength of the metallic filamentary material remains unimpaired by the process of encasing it in the matrix, so that an extremely favorable strengthto-weight ratio is obtained.
- the matrix material is deposited by a process which protects it from oxidation or other deleterious chemical action;
- the resulting composite shows exceptional resistance to erosion and cracking and high dimensional stability, when exposed to high temperature atmospheres.
- the composite material is therefore particularly useful in rocket nozzles and casings, and in other structures subjected to such atmospheres.
- the matrix material may be ceramic or metallic, and is preferably of a type having substantial resistance to erosion by chemical, thermal, or abrasive action.
- the method of this invention permits utilization of desirable combinations of matrix and filamentary materials in which the melting point of the former is higher than the recrystallization temperature of the latter.
- the matrix material In order to form a satisfactory structural material, it is necessary that the matrix material be caused to fully coalesce. However, if the matrix material is deposited en masse in a molten coalescing condition upon the filamentary material, and the recrystallization temperature of the latter is exceeded, the consequent grain growth of the filamentary material results in a substantial loss of the tensile strength of the filaments. The high strength characteristic which forms the principal advantage of such com posite materials is thereby lost.
- we carry out the method of our invention by first forming a plurality of fine elongated metallic filaments in a manner to develop a relatively high tensile strength therein, either by cold-drawing or by suitably heat-treating wire, or by utilizing whiskers in the asformed condition.
- the filaments may have a random orientation or may be arranged in a systematic orientation, either in a parallel linear form, or in a woven or transversely oriented relationship.
- Plasma-arc spraying techniques are preferably used, in which the matrix material is sprayed in line particles, by a stream of inert gas such as nitrogen, through an electric are which heats the particles at least to their melting point, and thence onto the mat.
- the particles coalesce upon the mat to form a dense solid matrix.
- the mass-rate of flow of the particles is held to a sulficiently small value to permit the average temperature of the filaments in the local area of deposition to remain below their recrystallization point.
- the mat may be placed or wound upon a chill block to assist in the dissipation of heat therefrom.
- the matrix material may be vaporized and deposited upon the mat in the presence of a vacuum or an inert atmosphere, although this is a relatively slow method.
- the composite material may be desirable to subject the composite material to a slight reduction in thickness by a rolling operation subsequent to the formation of the matrix, for the compaction of the latter.
- the material may then be subjected to heat treatment to render the matrix more malleable, a a temperature below the recrystallization temperature of the mat material.
- the composite structural material formed by our improved method exhibits a high strength to weight ratio corresponding to the original tensile strength of the fila ments; and affords unitary structures having excellent specific strength and specific modulus, resistance to thermal shock, heat transfer rate, impact strength, erosion and crack resistance, and ease of fabrication.
- the matrix material serves not only to resist erosion, but also to bond the filaments for transmission of shear stresses therebetween. If desired, a number of layers of filamentary mats and matrix material may be formed in subsequent steps to afford a structure of increased thickness.
- FIG. 1 is a view showing an illustrative method of winding a cylindrical mat of filamentary material in parallel orientation upon a mandrel;
- FIG. 2 is a plan view of a woven mat of filaments
- FIG. 3 is a plan view of a mat of filaments having a random orientation
- FIG. 4 is a schematic view showing a first technique for depositing matrix material upon a filamentary mat.
- FIG. 5 is a schematic view illustrating a technique for applying matrix material to a filamentary mat by vapor deposition.
- a selected material is first formed into filaments and treated to secure a high degree of tensile strength.
- cold-drawn or suitably heat-treated wire, or whisker crystals may be utilized in the as-formed condition.
- the filamentary material is then formed into a mat of any desired configuration and filament orientation.
- the filament is drawn from a supply reel 4 rotatably mounted upon a second shaft 5, and is subjected to a suitable winding tension by friction means (not shown).
- a guiding thimble 6 moves axially of the mandrel, being fed by means (not shown) drivingly connected with the shaft 3 to wind the mat in closely laid helical convolutions as the shaft rotates in the direction shown by the arrow.
- the mandrel 2 need not be cylindrical in form, but may for example comprise a fiat block to form a planar mat on either side thereof.
- the wire is initially secured upon a pin 7 fixed to the mandrel. Upon completion of the winding, the filament is broken and temporarily secured about a pin 8 fixed to the mandrel, or in any other suitable fashion.
- preferred means are shown for depositing a matrix 10 upon the mat to form a composite structure in accordance with our improved method.
- These means include a plasma-arc spray gun 11 of a wellknown type, in which an arc is generated between suitable electrodes (not shown) by an electric current supplied thereto by external electrical leads 12.
- a stream of inert gas such as nitrogen is supplied to the gun from a tank 14 through a conduit 15 having a pressure regulating valve 16, and issued at high velocity and high temperature from a spray nozzle 17 after passing through the aforementioned are and being ionized therein.
- a supply 18 of a selected finely particulated matrix material is placed in a hopper 19 and is fed at a desired rate to the nozzle 16 by a suitable aspirator comprising a branch conduit 20 and a feed screw 21.
- the feed screw is rotated at a preselected feed rate by a variable-speed motor 22 to feed the particles into the conduit, in which the particles are entrained by a flow of gas controlled by a pressure regulating valve 23.
- the flow of matrix material is entrained in the stream of inert gas flowing from the nozzle, and is heated thereby to a coalescible condition.
- a stream of the particles impinges with the gas stream upon the surface of the mat 1, coalescing thereon to form a rather dense matrix intimately bonded to the surface of the filament.
- a jet of cool inert gas may be caused to impinge upon the mat surface at an angle to the stream of hot gas carrying the matrix particles, to minimize oxidation of the matrix material and to aid in cooling the mat surface by sweeping away hot gases.
- the presence of oxides in the matrix tends to detract from crack resistance.
- the mass-flow rate of the particulated material to the mat is held to a sufficiently low value to permit the mat to dissipate heat from the coalescing particles rapidly enough to maintain the average temperature of the local area of deposition upon the mat below the recrystallization point of the filamentary material.
- the specific mass-flow rate varies widely and depends upon the size, melting point, and thermal capacity of the particles, the recrystallization point and thermal capacity of the filamentary material, and the rate of heat transfer to and heat dissipation from the mat and mandrel. However, an appropriate rate may readily be determined by experiment for a specific application, as will be apparent to those skilled in the art.
- the mandrel 2 is Continually rotated on the shaft 3 during the deposition step.
- the mandrel additionally serves as a chill block for the removal of heat from the mat by conduction.
- the filamentary material is not recrystallized, but substantially maintains its initially high tensile strength.
- the resulting composite structure therefore exhibits very high strength characteristics.
- the pins 7 and 8 are removed from the mandrel and from the composite structure. If desired, additional matrix material may be deposited upon the internal surface of the structure, but the external application results in a matrix of substantial thickness being formed on the internal surface by penetration of the particles between adjacent windings.
- filamentary material in the mat may be used, and a woven arrangement of filaments 24 is shown in FIG. 3.
- the filaments may be randomly oriented as illustrated by the loosely intertwined fibers 25 shown in FIG. 4.
- FIG. 5 there is shown an alternative method of deposition of the matrix material.
- a planar woven mat 27 is shown supported by a clamp 29 upon a stand 30, and is placed within a gas-tight container 31 upon a supporting surface 32.
- the container is evacuated by any suitable means (not shown) to afford an inert atmosphere, or filled with a suitable inert gas such as nitrogen.
- a crucible 34 containing a supply of the selected matrix material is placed in the container, and a pair of electrodes 35 are inserted in the matrix material.
- An electrical current is supplied by means of leads 37 to the electrodes, of a value suflicient to heat the matrix material to the point of vaporization.
- the vapor condenses upon the lower surface of the mat 27 at a low mass-rate to form extremely fine particles, which coalesce thereon to form a rather dense and well-bonded matrix.
- This method deposits the encasing matrix at a relatively slow rate, however.
- cold rolling may be utilized if desired, to further compact the matrix for the elimination of any minute voids therein. Only a small reduction in thickness is required for this purpose.
- the material may be heat-treated according to conventional techniques at a temperature lower than the recrystallization point of the filamentary material, to improve the malleability of the matrix.
- a filamentary mat of cold-drawn high-carbon steel wire having a diameter of .004 inch and an as-drawn tensile strength of 550,000 p.s.i. was prepared by winding the wire in parallel helical convolutions about a flat chill block.
- a matrix of aluminum particles having an average diameter of approximately 90 microns was deposited upon one exposed major surface of the mat by the plasma-arc spraying process to form a composite sheet having a total thickness of .006 inch. Additional layers of filamentary winding and matrix were applied to a total thickness of .035.045 inch.
- the sheet of composite material formed upon one surface of the chill block was then removed by cutting the filament about the edges of the block, and coldrolled to achieve a 5% reduction in thickness.
- the sheet was subjected to heat treatment at 500 F. for one-half hour to malleabilize the matrix.
- the filamentary material comprised 20% by volume of the composite sheet, which demonstrated a tensile strength, measured longitudinally of the wires, of 80,000 p.s.i.
- Another sheet was similarly prepared, but the steel wire comprised 3638% of the volume of the composite structure; a tensile strength ranging between 160,000 and 200,000 p.s.i. was demonstrated, again measured longitudinally of the wires.
- the composite material is useful in many applications, such as rocket nozzles and casings, for example, in which high strength-to-weight ratio, resistance to erosion and cracking, and dimensional stability in high temperature or erosive atmospheres, are of particular importance.
- a combination of tungsten wire matting with a tungsten matrix has been used to form a rocket nozzle throat and test-fired with highly satisfactory results.
- a throat having an initial diameter of 1.201 inches was fired for about 130 seconds at 5500 F., and showed a final diameter of 1.200 inches, the reduction being occasioned by a deposit of alumina from the propellant. There was no observable cracking or erosion after this firing.
- the metals suitable for use as the filamentary material include, without being limited to, iron, molybdenum, tungsten, tantalum, chromium, nickel, beryllium, columbium, rhenium, boron, cobalt, titanium, aluminum, and vanadium and their alloys.
- Suitable matrix materials include,
- whisker crystals as filamentary materials, it is to be noted that the ultimate tensile strength of all such materials is a relatively constant fraction of their respective moduli of elasticity. Therefore, the ratio of density to modulus of elasticity may be used as a convenient criterion for the choice of whisker materials to secure an optimum strength-to-weight ratio.
- suitable metallic whisker materials the following exhibit particularly low ratios of density to modulus of elasticity (figures are in units of IO- inches): beryllium-1.5; chromium5.8; molybdenum7.l; vanadium9.0; iron9.8.
- our improved method provides for the formation of composite structural materials having improved specific strength and specific modulus, resistance to thermal shock or other deterioration in high temperature atmospheres, heat transfer rate, impact strength, erosion and crack resistance, and ease of fabrication.
- the filamentary material affords a high overall tensile strength
- the matrix material may, if desired, be selected to afford low overall density and improved resistance to erosion by chemical, thermal, or abrasive action.
- rigid structures of any desired configuration may be prepared.
- the method of forming a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmosspheres which comprises the steps of: forming and treating fine elongated metallic filamentary material to obtain a crystal structure characterized by relatively high tensile strength which crystal structure tends to change to a crystal structure characterized by a lower tensile strength when said filamentary material is heated to the recrystallization temperature thereof; forming said filamentary material into a mat of a selected configuration; and encasing said mat in a substantially continuous coalescent matrix of a further material characterized by erosion resistance to high temperature atmospheres and having a melting point higher than the recrystallization temperature of said filamentary material, by depositing said further material by plasma arc spraying in an inert atmosphere upon said mat in fine coalescing particles at a mass-rate to maintain the average temperature of the area of deposition on said mat at a value less than the recrystallization temperature of said filamentary material.
- said matrix material is substantially free of oxides and is selected from the group consisting of metals, metal carbides, metal nitrides, metal bOtldES, metal silicides and graphite.
- the method of forming a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres which comprises the steps of: forming and treating fine elongated metallic filamentary material to obtain a crystal structure characterized by relatively high tensile strength which crystal structure tends to change to a crystal structure characterized by a lower tensile strength when said filamentary material is heated to the recrystallization temperature thereof; forming said filamentary material into a mat of a selected configuration; and encasing said mat in a substantially continuous coalescent matrix of metallic material having a melting point higher than the recrystallization temperature of said filamentary material, by depositing said matrix material by plasma arc spraying in an inert atmosphere upon said mat in fine coalescing particles at a mass-rate to maintain the average temperature of the area of deposition on said mat at a value less than the recrystallization temperature of said filamentary material.
- the method of forming a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres which comprises the steps of: forming a plurality of filamentary metal whisker crystals into a mat of a selected configuration, said whisker crystals being characterized by relatively high tensile strength Which strength tends to decrease when said whisker crystals are heated to the recrystallization temperature thereof; and encasing said mat in a substantially continuous coalescent matrix of material characterized by erosion resistance to high temperature atmospheres and having a melting point higher than the recrystallization temperature of said whisker crystals, by depositing said material by plasma arc spraying in an inert atmosphere upon said mat in fine coalescing particles at a mass-rate to maintain the average temperature of the area of deposition on said mat at a value less than the recrystallization temperature of said whisker crystals.
- a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 1.
- a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 3.
- a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 4.
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Description
Feb. 11, 1969 TH M ETAL 3,427,185
COMPOSITE STRUCTURAL MATERIAL INCORPORATING METALLIC FILAHENTS IN A MATRIX, AND METHOD OF MANUFACTURE Filed Feb. 19, 1964 i 'l 34 32 INVENTORS ROBERT G.CHEATHAM JOSEPH F. CHEATHAM FIGS MTW ATTORNEYS United States Patent Oflice 3,427,185 Patented Feb. 11, 1969 Claims ABSTRACT OF THE DISCLOSURE A high strength composite structural material resistant to high temperature atmospheres consisting of high tensile strength metallic filaments within a high temperature resistant matrix. The matrix material has a melting point higher than the recrystallization temperature of the filamentary material and is deposited onto a mat of filamentary material by plasma arc spraying in an inert atmosphere. In order to maintain the high tensile strength of the filamentary material, the rate of deposition of the matrix is controlled so that the filamentary material is maintained below its recrystallization temperature.
This invention relates to composite structural materials, and more particularly to an improved composite structural material incorporating metallic filaments in a matrix, which is characterized by a high strength-to-weight ratio and resistance to deterioration in high-temperature atmosphere, and a novel method of manufacture thereof. The present application is a continuation-in-part of our copending application S.N. 93,941, filed Mar. 7, 1961, now abandoned.
In the development of composite structural materials, intensive efforts are being made to discover structures and combinations of materials which will afford improvement in such characteristics as specific strength, specific modulus, resistance to thermal shock, heat transfer rate, impact strength, erosion and corrosion resistance, and ease of fabrication. It has been found that fine elongated filaments of metallic materials exhibit extraordinarily high tensile strengths. For example, while the tensile strength of steel in ordinary structural forms may fall in a range below 100,000 p.s.i., a cold-drawn steel wire .004 inch in diameter may exhibit a tensile strength in the range of 500,000 p.s.i. Even greater tensile strengths are found in whisker crystals, which may be defined as single crystals having screw dislocations but very few edge dislocations. The tensile strength of whisker crystals may approximate the atomic cohesion strength of the metal; in the case of iron whiskers, strengths of 1,900,000 p.s.i. have been shown, and in the case of copper crystals, 430,000 p.s.i., each exceeding the tensile strength of large sections of the same metals by a factor of more than ten. The reason for this great strength is not clearly understood, but may be based upon the low incidence of edge dislocations which can exist within the small diameter of whiskers.
We have found that, by our improved method, fine metallic filamentary materials in the form of fine wires or whisker crystals may be embedded in a coalescent matrix of further material to form a composite material which exhibits improved characteristics. The tensile strength of the metallic filamentary material remains unimpaired by the process of encasing it in the matrix, so that an extremely favorable strengthto-weight ratio is obtained. The matrix material is deposited by a process which protects it from oxidation or other deleterious chemical action; and
the resulting composite shows exceptional resistance to erosion and cracking and high dimensional stability, when exposed to high temperature atmospheres. The composite material is therefore particularly useful in rocket nozzles and casings, and in other structures subjected to such atmospheres. The matrix material may be ceramic or metallic, and is preferably of a type having substantial resistance to erosion by chemical, thermal, or abrasive action.
The method of this invention permits utilization of desirable combinations of matrix and filamentary materials in which the melting point of the former is higher than the recrystallization temperature of the latter. In order to form a satisfactory structural material, it is necessary that the matrix material be caused to fully coalesce. However, if the matrix material is deposited en masse in a molten coalescing condition upon the filamentary material, and the recrystallization temperature of the latter is exceeded, the consequent grain growth of the filamentary material results in a substantial loss of the tensile strength of the filaments. The high strength characteristic which forms the principal advantage of such com posite materials is thereby lost.
It is the primary object of the present invention to provide an improved method for forming a composite structural material having a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres. It is a further object to form an improved composite material from high tensile strength filaments and a coalescent matrix of a material whose melting point is higher than the recrystallization temperature of the filaments, without detracting from the tensile strength of the filaments. It is a further object of the invention to provide an improved method for forming a composite structural material through the practice of which improved physical characteristics may be achieved, particularly resistance to erosion and cracking, and dimensional stability when exposed to high temperature atmospheres. Further objects and advantages of the invention will become apparent as the following description proceeds.
Briefly stated, we carry out the method of our invention by first forming a plurality of fine elongated metallic filaments in a manner to develop a relatively high tensile strength therein, either by cold-drawing or by suitably heat-treating wire, or by utilizing whiskers in the asformed condition. We then form a plurality of the filaments into a mat of any desired structural form. The filaments may have a random orientation or may be arranged in a systematic orientation, either in a parallel linear form, or in a woven or transversely oriented relationship.
We then select a matrix material having resistance to erosion by high temperature atmospheres, and a melting point higher than the recrystallization temperature of the filaments. This material is deposited in an inert atmosphere upon the mat of filaments in fine coalescing particles, at such a mass-rate that heat dissipation by the mat is sufiiciently rapid to maintain the average temperature of the local area of deposition at a value less than the recrystallization temperature of the filaments. While the temperature in the immediate vicinity of impact of a particle may exceed the recrystallization temperature for a very brief interval, cooling occurs too rapidly to permit any deleterious grain modification to occur in the filaments.
Plasma-arc spraying techniques are preferably used, in which the matrix material is sprayed in line particles, by a stream of inert gas such as nitrogen, through an electric are which heats the particles at least to their melting point, and thence onto the mat. The particles coalesce upon the mat to form a dense solid matrix. The mass-rate of flow of the particles is held to a sulficiently small value to permit the average temperature of the filaments in the local area of deposition to remain below their recrystallization point. To this end, the mat may be placed or wound upon a chill block to assist in the dissipation of heat therefrom. Alternatively, the matrix material may be vaporized and deposited upon the mat in the presence of a vacuum or an inert atmosphere, although this is a relatively slow method.
In some instances it may be desirable to subject the composite material to a slight reduction in thickness by a rolling operation subsequent to the formation of the matrix, for the compaction of the latter. The material may then be subjected to heat treatment to render the matrix more malleable, a a temperature below the recrystallization temperature of the mat material.
The composite structural material formed by our improved method exhibits a high strength to weight ratio corresponding to the original tensile strength of the fila ments; and affords unitary structures having excellent specific strength and specific modulus, resistance to thermal shock, heat transfer rate, impact strength, erosion and crack resistance, and ease of fabrication. The matrix material serves not only to resist erosion, but also to bond the filaments for transmission of shear stresses therebetween. If desired, a number of layers of filamentary mats and matrix material may be formed in subsequent steps to afford a structure of increased thickness.
While the specification concludes with claims particularly pointing out the subject matter which we regard as our invention, it is believed that the invention will be more clearly understood from the following detailed description of preferred embodiments thereof, referring to the accompanying drawings, in which:
FIG. 1 is a view showing an illustrative method of winding a cylindrical mat of filamentary material in parallel orientation upon a mandrel;
FIG. 2 is a plan view of a woven mat of filaments;
FIG. 3 is a plan view of a mat of filaments having a random orientation;
FIG. 4 is a schematic view showing a first technique for depositing matrix material upon a filamentary mat; and
FIG. 5 is a schematic view illustrating a technique for applying matrix material to a filamentary mat by vapor deposition.
According to the invention, a selected material is first formed into filaments and treated to secure a high degree of tensile strength. For this purpose, cold-drawn or suitably heat-treated wire, or whisker crystals, may be utilized in the as-formed condition. The filamentary material is then formed into a mat of any desired configuration and filament orientation.
Referring to FIG. 1, there is shown an illustrative method for forming the mat. A cylindrical mat 1 of a selected continuous filamentary material, such as colddrawn wire, is wound about a mandrel 2 rotatably supported on a shaft 3 of a conventional winding lathe (not shown). The filament is drawn from a supply reel 4 rotatably mounted upon a second shaft 5, and is subjected to a suitable winding tension by friction means (not shown). A guiding thimble 6 moves axially of the mandrel, being fed by means (not shown) drivingly connected with the shaft 3 to wind the mat in closely laid helical convolutions as the shaft rotates in the direction shown by the arrow. The mandrel 2 need not be cylindrical in form, but may for example comprise a fiat block to form a planar mat on either side thereof. The wire is initially secured upon a pin 7 fixed to the mandrel. Upon completion of the winding, the filament is broken and temporarily secured about a pin 8 fixed to the mandrel, or in any other suitable fashion.
Referring now to FIG. 2, preferred means are shown for depositing a matrix 10 upon the mat to form a composite structure in accordance with our improved method. These means include a plasma-arc spray gun 11 of a wellknown type, in which an arc is generated between suitable electrodes (not shown) by an electric current supplied thereto by external electrical leads 12. A stream of inert gas such as nitrogen is supplied to the gun from a tank 14 through a conduit 15 having a pressure regulating valve 16, and issued at high velocity and high temperature from a spray nozzle 17 after passing through the aforementioned are and being ionized therein. A supply 18 of a selected finely particulated matrix material is placed in a hopper 19 and is fed at a desired rate to the nozzle 16 by a suitable aspirator comprising a branch conduit 20 and a feed screw 21. The feed screw is rotated at a preselected feed rate by a variable-speed motor 22 to feed the particles into the conduit, in which the particles are entrained by a flow of gas controlled by a pressure regulating valve 23. The flow of matrix material is entrained in the stream of inert gas flowing from the nozzle, and is heated thereby to a coalescible condition. A stream of the particles impinges with the gas stream upon the surface of the mat 1, coalescing thereon to form a rather dense matrix intimately bonded to the surface of the filament.
It may be found desirable to enclose the apparatus and the mat in a container and to establish an inert atmosphere therein, for preventing oxidation of the matrix material during the deposition step. Again, a jet of cool inert gas may be caused to impinge upon the mat surface at an angle to the stream of hot gas carrying the matrix particles, to minimize oxidation of the matrix material and to aid in cooling the mat surface by sweeping away hot gases. The presence of oxides in the matrix tends to detract from crack resistance.
The mass-flow rate of the particulated material to the mat is held to a sufficiently low value to permit the mat to dissipate heat from the coalescing particles rapidly enough to maintain the average temperature of the local area of deposition upon the mat below the recrystallization point of the filamentary material. The specific mass-flow rate varies widely and depends upon the size, melting point, and thermal capacity of the particles, the recrystallization point and thermal capacity of the filamentary material, and the rate of heat transfer to and heat dissipation from the mat and mandrel. However, an appropriate rate may readily be determined by experiment for a specific application, as will be apparent to those skilled in the art.
In order to assist in the rapid dissipation of heat, as well as to establish a uniform matrix thickness over the entire surface of the mat, the mandrel 2 is Continually rotated on the shaft 3 during the deposition step. The mandrel additionally serves as a chill block for the removal of heat from the mat by conduction. In consequence of the local mode of deposition of the matrix, and the relatively low mass-fiow rate of the matrix material onto the mat, the filamentary material is not recrystallized, but substantially maintains its initially high tensile strength. The resulting composite structure therefore exhibits very high strength characteristics. Following the deposition of the matrix, the pins 7 and 8 are removed from the mandrel and from the composite structure. If desired, additional matrix material may be deposited upon the internal surface of the structure, but the external application results in a matrix of substantial thickness being formed on the internal surface by penetration of the particles between adjacent windings.
Many alternative systematic orientations of the filamentary material in the mat may be used, and a woven arrangement of filaments 24 is shown in FIG. 3. Alternatively, the filaments may be randomly oriented as illustrated by the loosely intertwined fibers 25 shown in FIG. 4.
It will be apparent that a wide variety of structural forms may be produced by conforming a flexible mat of filamentary material to a mold of the desired configuration, and then depositing the matrix material upon the mat to produce a permanently formed composite structure. In some instances, it may be preferable to form the desired structural configuration from the finished composite material.
Referring now to FIG. 5, there is shown an alternative method of deposition of the matrix material. A planar woven mat 27 is shown supported by a clamp 29 upon a stand 30, and is placed within a gas-tight container 31 upon a supporting surface 32. The container is evacuated by any suitable means (not shown) to afford an inert atmosphere, or filled with a suitable inert gas such as nitrogen. A crucible 34 containing a supply of the selected matrix material is placed in the container, and a pair of electrodes 35 are inserted in the matrix material. An electrical current is supplied by means of leads 37 to the electrodes, of a value suflicient to heat the matrix material to the point of vaporization. The vapor condenses upon the lower surface of the mat 27 at a low mass-rate to form extremely fine particles, which coalesce thereon to form a rather dense and well-bonded matrix. This method deposits the encasing matrix at a relatively slow rate, however.
Following the deposition of the matrix upon the mat, cold rolling may be utilized if desired, to further compact the matrix for the elimination of any minute voids therein. Only a small reduction in thickness is required for this purpose. Following the cold-rolling operation, the material may be heat-treated according to conventional techniques at a temperature lower than the recrystallization point of the filamentary material, to improve the malleability of the matrix.
The following example is given to illustrate the advantages of a composite material prepared by our improved method. A filamentary mat of cold-drawn high-carbon steel wire having a diameter of .004 inch and an as-drawn tensile strength of 550,000 p.s.i. was prepared by winding the wire in parallel helical convolutions about a flat chill block. A matrix of aluminum particles having an average diameter of approximately 90 microns was deposited upon one exposed major surface of the mat by the plasma-arc spraying process to form a composite sheet having a total thickness of .006 inch. Additional layers of filamentary winding and matrix were applied to a total thickness of .035.045 inch. The sheet of composite material formed upon one surface of the chill block was then removed by cutting the filament about the edges of the block, and coldrolled to achieve a 5% reduction in thickness. The sheet was subjected to heat treatment at 500 F. for one-half hour to malleabilize the matrix. In this case, the filamentary material comprised 20% by volume of the composite sheet, which demonstrated a tensile strength, measured longitudinally of the wires, of 80,000 p.s.i. Another sheet was similarly prepared, but the steel wire comprised 3638% of the volume of the composite structure; a tensile strength ranging between 160,000 and 200,000 p.s.i. was demonstrated, again measured longitudinally of the wires.
The composite material is useful in many applications, such as rocket nozzles and casings, for example, in which high strength-to-weight ratio, resistance to erosion and cracking, and dimensional stability in high temperature or erosive atmospheres, are of particular importance. A combination of tungsten wire matting with a tungsten matrix has been used to form a rocket nozzle throat and test-fired with highly satisfactory results. A throat having an initial diameter of 1.201 inches was fired for about 130 seconds at 5500 F., and showed a final diameter of 1.200 inches, the reduction being occasioned by a deposit of alumina from the propellant. There was no observable cracking or erosion after this firing.
The metals suitable for use as the filamentary material include, without being limited to, iron, molybdenum, tungsten, tantalum, chromium, nickel, beryllium, columbium, rhenium, boron, cobalt, titanium, aluminum, and vanadium and their alloys. Suitable matrix materials include,
without being limited to, aluminum, titanium, magnesium,
and their alloys, cermets and certain ceramics such as carbides, nitrides, borides, silicides, aluminides, oxides and forms of graphite. To illustrate the selection of appropriate combinations of filamentary material and matrix material, the following table is given for comparison of the recrystallization temperatures of a variety of suitable filamentary materials with the melting points of various matrix materials:
F ILAMENTARY MATERIAL Minimum recrystallization temperature, deg. F. (approx) It will be understood that the foregoing list of materials is given purely for purposes of illustration, and it is not intended to limit the range of materials which may be selected in practicing the invention. The invention is particularly concerned with those combinations in which the melting point of the matrix material exceeds the recrystallization temperature of the filamentary material.
In the selection of whisker crystals as filamentary materials, it is to be noted that the ultimate tensile strength of all such materials is a relatively constant fraction of their respective moduli of elasticity. Therefore, the ratio of density to modulus of elasticity may be used as a convenient criterion for the choice of whisker materials to secure an optimum strength-to-weight ratio. Among suitable metallic whisker materials, the following exhibit particularly low ratios of density to modulus of elasticity (figures are in units of IO- inches): beryllium-1.5; chromium5.8; molybdenum7.l; vanadium9.0; iron9.8.
It will be apparent from the foregoing description that our improved method provides for the formation of composite structural materials having improved specific strength and specific modulus, resistance to thermal shock or other deterioration in high temperature atmospheres, heat transfer rate, impact strength, erosion and crack resistance, and ease of fabrication. In these structures, the filamentary material affords a high overall tensile strength, while the matrix material may, if desired, be selected to afford low overall density and improved resistance to erosion by chemical, thermal, or abrasive action. It will be apparent that by appropriate forming of a mat of filamentary material prior to the deposition of the matrix, rigid structures of any desired configuration may be prepared. Various changes and modifications will occur to those skilled in the art without departing from the true spirit and scope of the invention; we therefore intend to define the invention in the appended claims without limitation to specific illustrative embodiments herein described.
What we claim and desire to secure by Letters Patent of the United States is:
l. The method of forming a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmosspheres, which comprises the steps of: forming and treating fine elongated metallic filamentary material to obtain a crystal structure characterized by relatively high tensile strength which crystal structure tends to change to a crystal structure characterized by a lower tensile strength when said filamentary material is heated to the recrystallization temperature thereof; forming said filamentary material into a mat of a selected configuration; and encasing said mat in a substantially continuous coalescent matrix of a further material characterized by erosion resistance to high temperature atmospheres and having a melting point higher than the recrystallization temperature of said filamentary material, by depositing said further material by plasma arc spraying in an inert atmosphere upon said mat in fine coalescing particles at a mass-rate to maintain the average temperature of the area of deposition on said mat at a value less than the recrystallization temperature of said filamentary material.
2. The method of claim 1 wherein said matrix material is substantially free of oxides and is selected from the group consisting of metals, metal carbides, metal nitrides, metal bOtldES, metal silicides and graphite.
3. The method of claim 2 wherein said filamentary material is tungsten and said matrix material is tungsten.
4. The method of forming a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres, which comprises the steps of: forming and treating fine elongated metallic filamentary material to obtain a crystal structure characterized by relatively high tensile strength which crystal structure tends to change to a crystal structure characterized by a lower tensile strength when said filamentary material is heated to the recrystallization temperature thereof; forming said filamentary material into a mat of a selected configuration; and encasing said mat in a substantially continuous coalescent matrix of metallic material having a melting point higher than the recrystallization temperature of said filamentary material, by depositing said matrix material by plasma arc spraying in an inert atmosphere upon said mat in fine coalescing particles at a mass-rate to maintain the average temperature of the area of deposition on said mat at a value less than the recrystallization temperature of said filamentary material.
5. The method of forming a composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres, which comprises the steps of: forming a plurality of filamentary metal whisker crystals into a mat of a selected configuration, said whisker crystals being characterized by relatively high tensile strength Which strength tends to decrease when said whisker crystals are heated to the recrystallization temperature thereof; and encasing said mat in a substantially continuous coalescent matrix of material characterized by erosion resistance to high temperature atmospheres and having a melting point higher than the recrystallization temperature of said whisker crystals, by depositing said material by plasma arc spraying in an inert atmosphere upon said mat in fine coalescing particles at a mass-rate to maintain the average temperature of the area of deposition on said mat at a value less than the recrystallization temperature of said whisker crystals.
6. A composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 1.
7. A composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 2.
8. A composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 3.
9. A composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 4.
10. A composite structural material characterized by a high strength-to-weight ratio and resistance to deterioration in high temperature atmospheres produced by the process of claim 5.
References Cited UNITED STATES PATENTS 1,243,654 10/1917 Clark.
2,455,804 12/1948 Ransley et a]. 29-191.4 X 2,466,890 4/ 1949 Gilbertson.
2,924,004 2/1960 Wehrmann et al. 29-191.2 X 3,017,492 1/1962 Jepson 29-191.4 X 3,098,723 7/1963 Micks 29191.6 X 3,153,279 10/1964 Chessin 29-198 X 3,157,722 11/1964 Moore 29266 3,161,478 12/1964 Chessin 29191.2 3,156,040 11/1964 Drexhage.
3,257,803 6/1966 Reid 29-193 X OTHER REFERENCES Journal of Metals: January 1959, pp. 40-42, TN1J6 11793.1.
Metcalfe et al.: Metal Progress, March 1955, pp. 8185.
RALPH S. KENDALL, Primary Examiner.
US. Cl. X.R.
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US4782884A (en) * | 1987-02-04 | 1988-11-08 | General Electric Company | Method for continuous fabrication of fiber reinforced titanium-based composites |
US4786566A (en) * | 1987-02-04 | 1988-11-22 | General Electric Company | Silicon-carbide reinforced composites of titanium aluminide |
US4805294A (en) * | 1987-02-04 | 1989-02-21 | General Electric Company | Method for finishing the surface of plasma sprayed TI-alloy foils |
US4805833A (en) * | 1987-02-25 | 1989-02-21 | General Electric Company | Method of forming compacts with integral consolidation containers |
US4849152A (en) * | 1983-08-09 | 1989-07-18 | The Boeing Company | Cone control method for fabricating composite shafts |
US4865933A (en) * | 1984-08-22 | 1989-09-12 | Blanyer Richard J | Battery grid structure made of composite wire |
US4886202A (en) * | 1988-11-07 | 1989-12-12 | Westinghouse Electric Corp. | Method of making metal matrix monotape ribbon and composite components of irregular shape |
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EP0375914A1 (en) * | 1988-12-30 | 1990-07-04 | URANIT GmbH | Process for coating fibre-reinforced composites |
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US20210210220A1 (en) * | 2016-06-10 | 2021-07-08 | Westinghouse Electric Company Llc | Zirconium-coated silicon carbide fuel cladding for accident tolerant fuel application |
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US3889348A (en) * | 1969-03-27 | 1975-06-17 | Jerome H Lemelson | Fiber reinforced composite material and method of making same |
US3615277A (en) * | 1969-05-02 | 1971-10-26 | United Aircraft Corp | Method of fabricating fiber-reinforced articles and products produced thereby |
USRE28983E (en) * | 1970-02-23 | 1976-09-28 | Association Pour La Recherche Et Le Developpement Des Methodes Et Processus Industriels A.R.M.I.N.E.S. | Resistance and modulus reinforcing materials |
US3936277A (en) * | 1970-04-09 | 1976-02-03 | Mcdonnell Douglas Corporation | Aluminum alloy-boron fiber composite |
US3902864A (en) * | 1970-06-03 | 1975-09-02 | Gen Dynamics Corp | Composite material for making cutting and abrading tools |
US3876389A (en) * | 1970-06-30 | 1975-04-08 | Ibm | Composite material, inclusions thereof, and method therefor |
US3849080A (en) * | 1971-04-19 | 1974-11-19 | Maschf Augsburg Nuernberg Ag | Rotationally symmetrical hollow compound body |
US3994428A (en) * | 1972-05-04 | 1976-11-30 | Li Chou H | Apparatus for making reinforced metal-matrix composites |
US3900626A (en) * | 1973-09-04 | 1975-08-19 | United Aircraft Corp | Tantalum wire reinforced silicon nitride articles and method for making the same |
US3914500A (en) * | 1973-09-04 | 1975-10-21 | United Aircraft Corp | Tungsten wire reinforced silicon nitride articles and method for making the same |
US3953647A (en) * | 1973-10-05 | 1976-04-27 | United Technologies Corporation | Graphite fiber reinforced metal matrix composite |
US4091061A (en) * | 1974-07-05 | 1978-05-23 | Engins Matra | Method for the production of mouldings containing reinforcing fibre type filler |
US4300951A (en) * | 1978-02-24 | 1981-11-17 | Kabushiki Kaisha Fujikoshi | Liquid phase sintered dense composite bodies and method for producing the same |
US4239833A (en) * | 1978-12-28 | 1980-12-16 | Mennica Panstwowa | Grid of precious metals for the recovery of platinum metals escaping from a catalyst during the reaction, and especially of platinum during oxidation of ammonia |
US5404639A (en) * | 1980-07-02 | 1995-04-11 | Dana Corporation | Composite insulation for engine components |
US4412859A (en) * | 1981-08-12 | 1983-11-01 | Engelhard Corporation | Method for recovering platinum in a nitric acid plant |
WO1983001751A1 (en) * | 1981-11-17 | 1983-05-26 | United Technologies Corp | Plasma coatings comprised of sprayed fibers |
EP0093779A1 (en) * | 1981-11-17 | 1983-11-16 | United Technologies Corp | Plasma coatings comprised of sprayed fibers. |
EP0093779A4 (en) * | 1981-11-17 | 1984-06-29 | United Technologies Corp | Plasma coatings comprised of sprayed fibers. |
US4595637A (en) * | 1981-11-17 | 1986-06-17 | United Technologies Corporation | Plasma coatings comprised of sprayed fibers |
FR2538507A1 (en) * | 1982-12-22 | 1984-06-29 | Messerschmitt Boelkow Blohm | Ablation lining for combustion chamber walls |
US4849152A (en) * | 1983-08-09 | 1989-07-18 | The Boeing Company | Cone control method for fabricating composite shafts |
US4631793A (en) * | 1984-01-27 | 1986-12-30 | Chugai Ro Co., Ltd. | Fiber reinforced metal alloy and method for the manufacture thereof |
WO1985005173A1 (en) * | 1984-05-02 | 1985-11-21 | General Electric Company | Wear resistant gun barrel and method of forming |
US4577431A (en) * | 1984-05-02 | 1986-03-25 | General Electric Company | Wear resistant gun barrel and method of forming |
EP0339692A3 (en) * | 1984-05-02 | 1990-01-31 | General Electric Company | Method of forming a wear resistant gun barrel |
EP0339692A2 (en) * | 1984-05-02 | 1989-11-02 | General Electric Company | Method of forming a wear resistant gun barrel |
US4865933A (en) * | 1984-08-22 | 1989-09-12 | Blanyer Richard J | Battery grid structure made of composite wire |
DE3638088A1 (en) * | 1986-11-07 | 1988-05-19 | Bernd Retter | Process and apparatus for coating wearing surfaces and wearing surfaces produced by the process |
US4805294A (en) * | 1987-02-04 | 1989-02-21 | General Electric Company | Method for finishing the surface of plasma sprayed TI-alloy foils |
US4782884A (en) * | 1987-02-04 | 1988-11-08 | General Electric Company | Method for continuous fabrication of fiber reinforced titanium-based composites |
EP0358800A1 (en) * | 1987-02-04 | 1990-03-21 | General Electric Company | Method for finishing the surface of plasma sprayed titanium-based alloy foils |
EP0358802A1 (en) * | 1987-02-04 | 1990-03-21 | General Electric Company | Method for fabricating titanium alloys in foil form |
EP0358801A1 (en) * | 1987-02-04 | 1990-03-21 | General Electric Company | Method for continuous fabrication of fiber reinforced titanium-based composites |
EP0358799A1 (en) * | 1987-02-04 | 1990-03-21 | General Electric Company | Silicon-carbide reinforced composites of titanium aluminide |
US4786566A (en) * | 1987-02-04 | 1988-11-22 | General Electric Company | Silicon-carbide reinforced composites of titanium aluminide |
US4805833A (en) * | 1987-02-25 | 1989-02-21 | General Electric Company | Method of forming compacts with integral consolidation containers |
EP0363655A1 (en) * | 1988-10-14 | 1990-04-18 | Westinghouse Electric Corporation | Use of ac power in arc spray process |
US4886202A (en) * | 1988-11-07 | 1989-12-12 | Westinghouse Electric Corp. | Method of making metal matrix monotape ribbon and composite components of irregular shape |
EP0375914A1 (en) * | 1988-12-30 | 1990-07-04 | URANIT GmbH | Process for coating fibre-reinforced composites |
US5211776A (en) * | 1989-07-17 | 1993-05-18 | General Dynamics Corp., Air Defense Systems Division | Fabrication of metal and ceramic matrix composites |
US6592965B1 (en) | 1990-07-06 | 2003-07-15 | Igr Enterprises, Inc. | Ductile ceramic composite electrolyte |
US5332483A (en) * | 1990-07-06 | 1994-07-26 | Igr Enterprises, Inc. | Gas separation system |
WO1992000934A3 (en) * | 1990-07-06 | 1992-09-03 | Igr Ets Inc | Ductile ceramic composites |
WO1992000934A2 (en) * | 1990-07-06 | 1992-01-23 | Igr Enterprises, Inc. | Ductile ceramic composites |
US5440806A (en) * | 1992-03-13 | 1995-08-15 | Mtu Motoren- Und Turbinen-Union Muenchen Gmbh | Method of making blank for the manufacturing of fiber-reinforced coatings or metal components |
US5557846A (en) * | 1992-03-13 | 1996-09-24 | Mtu Motoren- Und Turbinen-Union Muenchen Gmbh | Blank for the manufacturing of fiber reinforced coatings or metal components |
US5338497A (en) * | 1992-04-03 | 1994-08-16 | Ford Motor Company | Induction heating method for forming composite articles |
FR2761619A1 (en) * | 1997-04-07 | 1998-10-09 | Ca Nat Research Council | METHOD FOR PRODUCING REINFORCED COMPOSITE PROFILES WITH METAL MATRIX AND AXIAL SYMMETRY |
US20060210819A1 (en) * | 2005-03-15 | 2006-09-21 | Dueber Thomas E | Polyimide composite coverlays and methods and compositions relating thereto |
US20210210220A1 (en) * | 2016-06-10 | 2021-07-08 | Westinghouse Electric Company Llc | Zirconium-coated silicon carbide fuel cladding for accident tolerant fuel application |
US11862351B2 (en) * | 2016-06-10 | 2024-01-02 | Westinghouse Electric Company Llc | Zirconium-coated silicon carbide fuel cladding for accident tolerant fuel application |
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