US3177084A - Method of making carbide-coated graphite dies and coated article - Google Patents

Method of making carbide-coated graphite dies and coated article Download PDF

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US3177084A
US3177084A US104466A US10446661A US3177084A US 3177084 A US3177084 A US 3177084A US 104466 A US104466 A US 104466A US 10446661 A US10446661 A US 10446661A US 3177084 A US3177084 A US 3177084A
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die
carbide
titanium
film
hydrogen
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Amstein Edmund Hollis
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British Aluminum Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/52Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbon, e.g. graphite
    • C04B35/522Graphite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21JFORGING; HAMMERING; PRESSING METAL; RIVETING; FORGE FURNACES
    • B21J13/00Details of machines for forging, pressing, or hammering
    • B21J13/02Dies or mountings therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C3/00Selection of compositions for coating the surfaces of moulds, cores, or patterns
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/58Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
    • C04B35/5805Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on borides
    • C04B35/58064Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on borides based on refractory borides
    • C04B35/58071Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on borides based on refractory borides based on titanium borides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • C04B35/645Pressure sintering
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/50Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
    • C04B41/5053Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials non-oxide ceramics
    • C04B41/5057Carbides
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/30Self-sustaining carbon mass or layer with impregnant or other layer

Definitions

  • This invention relates to improvements in dies and is particularly concerned with improvements in graphite dies for use in high temperature hot pressing processes which are performed at temperatures above 1000 C., e.g., up to about 2300 C., and in a method of producing same.
  • Dies for use in high temperature hot pressing processes which are performed at temperatures above 1000 C. are commonly made of graphite in view of the resistance of this material to the high temperatures and pressures involved.
  • the material to be hot pressed may be one which either reacts with or is mutually soluble in the material of the die at the pressing temperature and in these cases there is a tendency for the hot pressed body to stick to the die. Where such sticking occurs the least harmful result is that a new die has to be used for each pressing operation thereby adding considerably to the cost. It is quite possible, however, that sticking may cause the die to break before the pressing operation is completed, or it may result in the pressed body breaking during cooling as a result of the differential contraction of the die and the body.
  • the surface or surfaces of the wall or walls defining the cavity in a graphite die for use in a high temperature hot pressing process is or are coated with a film of a carbide of one of the transition elements in Groups IV, V and VI of the Periodic System.
  • the carbide is preferably titanium carbide.
  • a method of manufacturing a graphite die for use in a high temperature hot pressing process comprises the step of coating the surface or surfaces of the wall or walls defining the die cavity with a film of a carbide of one of the transition elements in Groups IV, V and VI of the Perodic System.
  • the carbide is preferably titanium carbide and it may be applied to the surface or surfaces in the form of a suspension of titanium carbide in butyl titanate paint medium and subsequently fired on to said surface or surfaces.
  • the film of titanium carbide may be produced by heating the die, which is of graphite, and passing a mixture of vaporised titanium chloride and hydrogen over the surface or surfaces to form the film of titanium carbide thereon.
  • the film of titanium carbide is fired on to the surface or surfaces e.g., by heating the die to a temperature of the order of 2,000 C. in an atmosphere of hydrogen.
  • the carbide coating is applied to the graphite die surface in a moistened condition either by contacting the die cavity or bore surface or surfaces with an aqueous slurry of the carbide, or by sprinkling carbide dust onto the previously wetted die cavity surface.
  • the carbide is applied in a moistened condition the coating is fired in situ; that is, the coating is fired onto the die surface during the hot pressing operation.
  • the powder or material to be hot pressed is loaded into the die after coating the die cavity surface as above described, and the loaded die is then placed into a hot pressing assembly. As the assembly is brought up to the hot pressing temperature, the moisture is removed from the carbide coating, and the coating is fired onto the die cavity surface.
  • FIGURE 1 illustrates diagrammatically one way of carrying the invention into effect
  • FIGURE 2 is a view similar to FIGURE 1 illustrating a modification
  • FIGURE 3 is a view similar to FIGURE 1 illustrating a further modification
  • FIGURE 4 is a sectional view taken on the line IV- IV 'of FIGURE 5 of a cylindrical die according to the invention.
  • FIGURE 5 is a section taken on the line VV of FIGURE 4.
  • the surface or surfaces of the wall or walls defining the cavity of a graphite die may be coated with a film of a carbide of one of the transition elements in Groups IV, V and VI of the Periodic System by coating the surface or surfaces with a paint composed of the carbide of the transition element suspended in a suitable medium, the film so produced being allowed to dry and being fired on to the surface at an appropriate temperature in a protective atmosphere.
  • a film of the carbide of one of the transition elements in Group IV or V may be produced by vaporizing or subliming, as the case may be, the tetrachloride of the transition element and passing it in admixture with hydrogen over the surface or surfaces of the die whilst the latter is heated to a temperature sufiicient to cause the graphite of the die to react with the tetrachloride of the transition element to produce the carbide of the latter with the formation of hydrogen chloride due to the hydrogen present in the gaseous mixture, the carbide being deposited as a film of substantially uniform thickness on the surface or surfaces and desirably being subsequently fired thereon at an appropriate temperature in a protective atmosphere.
  • a film of the carbide of a transition element in Group VI may be produced on the surface or surfaces of the wall or walls defining the die cavity by exposing the surface or surfaces to a gaseous mixture of hydrogen and the carbonyl of the transition element at a reduced pressure of from 0.1 to 10 mm. of mercury and heating the die to a temperature sufiicient to cause the hydrogen to reduce the carbonyl to produce the carbide of the transition element which carbide is deposited as a film of substantially uniform thickness on the surface or surfaces, the carbide film being subsequently fired on to the surface or surfaces at a temperature between 2000 C.-2l00 C. in a protective atmosphere e.g., hydrogen.
  • the firing may alternatively be effected after the powder to be pressed is loaded into the die and during the high temperature hot pressing operation.
  • a paint composed of titanium carbide suspended in butyl titanate paint medium is prepared by ball-milling the titanium carbide in the butyl titanate for some hours, e.g., 8 hours.
  • the surface or surfaces of the wall or walls defining the die cavity is or are then painted with the suspension and the film so produced is allowed to dry for one or more hours.
  • the film is then fired on to the surface or surfaces by heating the die to a temperature of the order of 2000 C. in an atmosphere of hydrogen.
  • Butyl titanate is preferred as the paint medium because its ultimate decomposition product is titanium dioxide which is reduced to give titanium carbide during the high temperature firing operation.
  • An example of coating the surface or surfaces of the wall or walls of a graphite die with titanium carbide by this method is as follows: Liquid titanium tetrachloride 1 (FIGURE 1), contained in a suitable glass vessel 2, is heated to a temperature of 100 C.
  • the glass vessel 2 is closed by a glass plug '7 through which extends a tube 8 opening into the space above the liquid titanium tetrachloride in the vessel 2 and communicating with the interior of a cylindrical graphite die 9.
  • a branch tube 10 connects the tube 8 to the hydrogen source 4 and a tap 11 is connected in the tube 10.
  • the hydrogen source 4 is connected to both the tubes 5 and 10 by a common tube 12 in which there is provided a further tap 13 whereby the hydrogen source may be isolated from the rest of the system.
  • the die 9 is heated in any suitable manner, for example, by the electric heating coil 14 shown in FIGURE 1 which is connected by way of terminals 14a to a suitable source of supply.
  • the water-bath 3 vaporizes the titanium tetrachloride and, with the taps 6 and 13 open and the tap 11 closed, a mixture of vaporized titanium chloride and hydrogen flows into the cavity or interior of the die 9 so that the surface of the wall thereof is exposed to this mixture.
  • the die 9 is heated by the coil 14 to a temperature of from 1500 C.1600 C., e.g., 1550 C. and the mixture of vaporized titanium chloride and hydrogen is caused to flow through the die 9 for a period of one to two hours, e.g., one hour.
  • the end of the die 9 remote from the tube 8 is restricted by a plug and the gases issue from this end as a jet which is ignited.
  • the carbon of the die reacts with the titanium tetrachloride to form a film of titanium carbide on the internal wall of the die 9 and at the end of this period the tap 6 is closed and the tap 11 is opened so that the supply of vaporized titanium tetrachloride is discontinued and hydrogen only passes to the interior of the die 9, the latter now being heated by the coil 14 to a temperature of about 2050 C. for a short period of the order of 15 minutes and then being allowed to cool, the hydrogen atmosphere being mamtained during the cooling of the die.
  • This high temperature heating improves the adherence of the titanium carbide to the die and removes any free titanium metal which might be present in the film by converting it to the carbide.
  • the procedure described above may be used to coat the interior of the die 9 with vanadium carbide by substituting vanadium tetrachloride for the titanium tetrachloride in the vessel 2.
  • the procedure described above is modified as shown in FIGURE 2 by substituting a copper tube 15 for the vessel 2 and water bath 3.
  • a copper tube 15 for the vessel 2 and water bath 3.
  • the zirconium tetrachloride is disposed in the copper tube 15 and is heated by any suitable means such as, for example,
  • a tubular wire wound resistance furnace indicated very diagrammatically by the heating coil 16, to a temperature of from 250 C.300 C., e.g., 270 C. and hydrogen gas is passed through the tube 15 from the source 4 for a period of one to two hours as before and the mixture of hydrogen and zirconium tetrachloride passed into the die 9, which latter is in this case maintained at a temperature of between 1700 C. and 1900" C.
  • the Zirconium tetrachloride reacts with the carbon of the die to form zirconium carbide as a film on the interior of the die 9 and at the end of the period the tap 6 is closed and the tap 11 is opened so that hydrogen is supplied to the interior of the die 9 whilst the latter is now heated by the coil 14 to a temperature of at least 2,100 C. for a short period of the order of 15 minutes after which it is allowed to cool whilst maintaining the atmosphere of hydrogen.
  • the method of producing a film of the carbide of a transition element in Group VI using the carbonyl of the transition element is as follows:
  • the die 9 (FIG. 3) is disposed in a vacuum furnace 17 the interior of which is connected by a pipe 18 through a tap 19 to a vacuum pump 20.
  • the interior of the furnace 17 is also connected by a pipe 21 through a tap 22 to a container 23 containing the carbonyl of the transition element, e.g., molybdenum carbonyl (Mo(CO) which is a solid at normal temperature and pressure.
  • the interior of the container 23 is connected by a pipe 24 and a tap 25 to a source 26 of hydrogen under pressure.
  • the die 9 is heated to a temperature of about 500 C.
  • the tap 19 is opened and the pump 20 operated to reduce the pressure in the furnace 17 to below 0.1 mm. of mercury.
  • the taps 22 and 25 are opened to cause a gaseous mixture of hydrogen and the carbonyl to flow into the furnace 17, the taps 19 and 22 being adjusted to control the rate of flow of this gaseous mixture and the pressure within the furnace 1'7, this pressure being maintained at about 5 mm. of mercury and the rate of flow of the gaseous mixture being about /2 litre/min.
  • the carbonyls of the transition elements in Group VI are solids at N.T.P. their vapor pressure is suflicient to provide the required quantity of gaseous carbonyl at the reduced pressure existing in the furnace 17.
  • the gaseous mixture is allowed to flow into and through the furnace 17 for a period of at least 2 hours during which period the hydrogen reduces the carbonyl to the carbide which is deposited on the surface or surfaces of the die.
  • the die 9 is cooled in a vacuum, and is subsequently removed from the furnace 17 and transferred to a high temperature furnace where it is heated to a temperature of 2000 C.2l00 C. in a protective atmosphere, e.g., hydrogen, for a period of about 15 minutes and allowed to cool whilst the protective atmosphere is maintained in order to tire the carbide film on to the surface or surfaces of the die.
  • a protective atmosphere e.g., hydrogen
  • a mixture of finely ground carbide powder and water is first prepared. Upon agitation the fine powder will be suspended within the aqueous medium.
  • the coating is applied by temporarily sealing the lower end of the die in such a manner as to plug the cavity or bore.
  • the aqueous slurry is then introduced into the die cavity and agitated.
  • the slurry may be additionally agitated prior to introduction to the die cavity in order to ensure a suitable suspension of the carbide powder.
  • the carbide particles will come out of the slurry and adhere to the surface or surfaces of the die cavity forming the desired film.
  • Excess water and the temporary seal or plug are removed from the die cavity and the die is then loaded with the powder to be pressed.
  • Protective gas such as argon, nitrogen, or hydrogen is introduced to the die cavity at the beginning of the pressing operation.
  • the hot pressing die assembly is brought up to the temperature for hot pressing the moisture is removed, and the carbide film is subjected to a temperature of at least about 2000 C. to fire the coating onto the said surface or surfaces.
  • the contacting of the surface or surfaces of the die cavity with the aqueous-carbide mixture or slurry may be accomplished by painting or brushing the slurry on to the said surface or surfaces.
  • the desired carbide coating may be applied by first wetting the surface or surfaces of the die cavity with water in any convenient manner. Finely ground carbide powder is then dusted onto the wet surface. The so treated die is installed in the furnace, and the powder to be pressed is loaded into the die and subjected to the hot pressing operation.
  • the aqueous medium in these methods acts as an adhesive enabling the carbide to remain on the die until the powder to be pressed is introduced into the die.
  • the powder when in the die supports the carbide material on the die wall and prevents it from flaking off as would occur when the aqueous mixture is dried.
  • the firing of the carbide coating can be accomplished either prior to the addition of the powder to the die or after the powder is introduced and during the hot pressing thereof.
  • FIGURES 4 and 5 illustrate a cylindrical graphite die 9 having a coating 27 of carbide in accordance with this invention, the thickness of this coating being exaggerated for the purpose of illustration.
  • FIGURE 4 also shows two plungers 28 which may be hydraulically operated for the purpose of exerting a pressure on any powdered material placed in the die 9 for hot pressing to the shape of a rod.
  • a graphite die 9 having a carbide coating 27 in accordance with this invention is of particular, but not exclusive, application in the hot pressing of the diborides of titanium and zirconium.
  • titanium diboride is hot pressed in a graphite die at a temperature of the order of 2000 C.
  • the titanium diboride to stick to the die with the result that the latter breaks before the pressing operation is completed, or the pressed body of titanium diboride breaks during cooling as a result of the differential contraction of the die and the pressed body.
  • These difliculties are not encountered when the hot pressing operation is performed at a temperature below 1700 C. but it is not possible to produce a satisfactory strong and dense body at such low temperatures.
  • titanium diboride and carbon have some mutual solubility at temperatures of the order of 2000 C. or above or that the effect may be due to small amounts of impurity, such as boric oxide (B 0 which it is not economic to remove from the titanium diboride powder.
  • impurity such as boric oxide (B 0 which it is not economic to remove from the titanium diboride powder.
  • B 0 boric oxide
  • titanium diboride may be satisfactorily hot pressed at temperatures of the order of 2000 C. and above in a graphite die when the surface or surfaces of the wall or walls defining the cavity in the die is or are coated with a film of the carbide of one of the transition elements in Groups IV, V and VI of the Periodic System, e.g., titanium carbide.
  • Reasonable hot pressed bodies of titanium diboride may be produced in graphite dies treated by the first method described above, i.e., by painting and firing, but it is extremely desirable, if not essential, that the painting and firing be repeated after each pressing operation.
  • Titanium diboride can be hot pressed at the highest temperatures normally used (about 2050 C.) in a die treated by any of the other methods described above without sticking occurring and a number of pressings (at least six) can be obtained from a given die without further treatment.
  • a powder of titanium diboride was hot-pressed in a cylindrical graphite die 9 such as illustrated in FIGURE 4 at a maximum temperature of 2050 C. and a maximum pressure of 1 ton/sq. in. on the plungers 28.
  • the surface of the die 9 defining the cavity was coated with titanium carbide by the tetrachloride method described above.
  • the resultant titanium diboride bar had a low porosity of the order of 6% by volume and a transverse rupture modulus of about 15 tons per sq. in. No sticking of the titanium diboride to the die 9 occurred and the surface of the die 9 defining the cavity was unimpaired and the die 9 was suitable for further operations.
  • a film of titanium carbide on the surface or surfaces of the wall or walls defining the die cavity is beneficial not only in the hot pressing of titanium diboride and the borides or diborides of the other transition elements in Groups IV, V and VI of the Periodic System but is also beneficial for the hot pressing of the carbides of such elements.
  • the soft graphite dies do score in use and often have to be discarded for this reason alone.
  • the treated dies show no signs of scoring since the film is both hard and durable. This film is also helpful in minimizing die reaction in cases where the material being hot pressed reacts with the material of the die.
  • oxide ceramics tend to react with the graphite of the die during pressing, but oxides are in general much less reactive towards titanium carbide.
  • titanium carbide, vanadium carbide, zirconium carbide or molybdenum carbide on the surface or surfaces of the wall or walls of the die cavity it is not limited to the film being of one of these carbides as it is within the scope of the invention to provide such a film of a carbide of any one of the transition elements of Groups 1V, V and VI of the Periodic System, namely, titanium, zirconium and hafnium, vanadium, niobium and tantalum and chromium, molybdenum and tungsten.
  • titanium tetrachloride is both the cheapest and most freely available material for producing a suitable film on the surface or surfaces of the wall or Walls of the die cavity so that it is most economic to form the film from titanium carbide.
  • a graphite die for use in a high temperature hot pressing process having disposed on the surfaces defining a die cavity a fired coating comprising a film of a carbide of a metal selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum and tungsten, said film containing no free metal.
  • a graphite die as in claim 1 wherein the fired coating is titanium carbide.
  • a graphite die as in claim 1 wherein the fired coating is zirconium carbide.
  • a graphite die as in claim 1 wherein the fired coating is molybdenum carbide.

Description

Apnl 6, 1965 E. H. AMSTEIN 3,177,084
METHOD OF MAKING CARBIDE-COATED GRAPHITE DIES AND COATED ARTICLE Filed April 20. 1961 INVENTOR EDMUND HOLLIS AMSTEIN ATTORNEY United States Patent 3,177,084 METHOD OF MAKING CIDE-COATED GRAPH- ITE DIES AND COATED ARTICLE Edmund Hollis Amstein, Chester, England, assignor to The British Aluminium Company Limited, London, England, a company of Great Britain Filed Apr. 20, 11961, Ser. No. 104,466 Claims priority, application Great Britain, Aug. 23, 1956, 25,822/ 56 5 Claims. (Cl. 1175.1)
This invention relates to improvements in dies and is particularly concerned with improvements in graphite dies for use in high temperature hot pressing processes which are performed at temperatures above 1000 C., e.g., up to about 2300 C., and in a method of producing same.
This application is a continuation-in-part of copending application, S.N. 679,387, entitled Method of Making Carbide Coated Graphite Dies and Coated Article, filed August 21, 1957, now abandoned.
Dies for use in high temperature hot pressing processes which are performed at temperatures above 1000 C. are commonly made of graphite in view of the resistance of this material to the high temperatures and pressures involved. In some cases, however, the material to be hot pressed may be one which either reacts with or is mutually soluble in the material of the die at the pressing temperature and in these cases there is a tendency for the hot pressed body to stick to the die. Where such sticking occurs the least harmful result is that a new die has to be used for each pressing operation thereby adding considerably to the cost. It is quite possible, however, that sticking may cause the die to break before the pressing operation is completed, or it may result in the pressed body breaking during cooling as a result of the differential contraction of the die and the body.
It is an object of the present invention to provide an improved die for use in high temperature hot pressing processes which shall not be subject to the disadvantages referred to.
According to one feature of the present invention the surface or surfaces of the wall or walls defining the cavity in a graphite die for use in a high temperature hot pressing process is or are coated with a film of a carbide of one of the transition elements in Groups IV, V and VI of the Periodic System.
The carbide is preferably titanium carbide.
According to another feature of the present invention, a method of manufacturing a graphite die for use in a high temperature hot pressing process comprises the step of coating the surface or surfaces of the wall or walls defining the die cavity with a film of a carbide of one of the transition elements in Groups IV, V and VI of the Perodic System.
The carbide is preferably titanium carbide and it may be applied to the surface or surfaces in the form of a suspension of titanium carbide in butyl titanate paint medium and subsequently fired on to said surface or surfaces. Alternatively the film of titanium carbide may be produced by heating the die, which is of graphite, and passing a mixture of vaporised titanium chloride and hydrogen over the surface or surfaces to form the film of titanium carbide thereon. Preferably the film of titanium carbide is fired on to the surface or surfaces e.g., by heating the die to a temperature of the order of 2,000 C. in an atmosphere of hydrogen.
In another embodiment of the invention, the carbide coating is applied to the graphite die surface in a moistened condition either by contacting the die cavity or bore surface or surfaces with an aqueous slurry of the carbide, or by sprinkling carbide dust onto the previously wetted die cavity surface. When the carbide is applied in a moistened condition the coating is fired in situ; that is, the coating is fired onto the die surface during the hot pressing operation. The powder or material to be hot pressed is loaded into the die after coating the die cavity surface as above described, and the loaded die is then placed into a hot pressing assembly. As the assembly is brought up to the hot pressing temperature, the moisture is removed from the carbide coating, and the coating is fired onto the die cavity surface. I
The invention will now be described by way of example, reference being made to the accompanying drawings in which:
FIGURE 1 illustrates diagrammatically one way of carrying the invention into effect,
FIGURE 2 is a view similar to FIGURE 1 illustrating a modification,
FIGURE 3 is a view similar to FIGURE 1 illustrating a further modification,
FIGURE 4 is a sectional view taken on the line IV- IV 'of FIGURE 5 of a cylindrical die according to the invention, and
FIGURE 5 is a section taken on the line VV of FIGURE 4.
The surface or surfaces of the wall or walls defining the cavity of a graphite die may be coated with a film of a carbide of one of the transition elements in Groups IV, V and VI of the Periodic System by coating the surface or surfaces with a paint composed of the carbide of the transition element suspended in a suitable medium, the film so produced being allowed to dry and being fired on to the surface at an appropriate temperature in a protective atmosphere. Alternatively a film of the carbide of one of the transition elements in Group IV or V may be produced by vaporizing or subliming, as the case may be, the tetrachloride of the transition element and passing it in admixture with hydrogen over the surface or surfaces of the die whilst the latter is heated to a temperature sufiicient to cause the graphite of the die to react with the tetrachloride of the transition element to produce the carbide of the latter with the formation of hydrogen chloride due to the hydrogen present in the gaseous mixture, the carbide being deposited as a film of substantially uniform thickness on the surface or surfaces and desirably being subsequently fired thereon at an appropriate temperature in a protective atmosphere. A film of the carbide of a transition element in Group VI may be produced on the surface or surfaces of the wall or walls defining the die cavity by exposing the surface or surfaces to a gaseous mixture of hydrogen and the carbonyl of the transition element at a reduced pressure of from 0.1 to 10 mm. of mercury and heating the die to a temperature sufiicient to cause the hydrogen to reduce the carbonyl to produce the carbide of the transition element which carbide is deposited as a film of substantially uniform thickness on the surface or surfaces, the carbide film being subsequently fired on to the surface or surfaces at a temperature between 2000 C.-2l00 C. in a protective atmosphere e.g., hydrogen. When the carbide coating is applied by contacting the die surface with an aqueous slurry of the carbide or by dusting onto a previously wetted die surface, the firing may alternatively be effected after the powder to be pressed is loaded into the die and during the high temperature hot pressing operation.
An example of the first of these methods is as follows: a paint composed of titanium carbide suspended in butyl titanate paint medium is prepared by ball-milling the titanium carbide in the butyl titanate for some hours, e.g., 8 hours. The surface or surfaces of the wall or walls defining the die cavity is or are then painted with the suspension and the film so produced is allowed to dry for one or more hours. The film is then fired on to the surface or surfaces by heating the die to a temperature of the order of 2000 C. in an atmosphere of hydrogen. Butyl titanate is preferred as the paint medium because its ultimate decomposition product is titanium dioxide which is reduced to give titanium carbide during the high temperature firing operation.
The method of producing a film of the carbide of a transition element in Group IV or V using the tetrachloride of the transition element is based on the reaction MCl +C+2H =MC+4HCl (where M is the transition element) which can, under suitable conditions, produce a film of the carbide of the transition element on carbon. An example of coating the surface or surfaces of the wall or walls of a graphite die with titanium carbide by this method is as follows: Liquid titanium tetrachloride 1 (FIGURE 1), contained in a suitable glass vessel 2, is heated to a temperature of 100 C. in a water bath 3 and hydrogen is passed through it at about 4 litres per minute from a source 4 of hydrogen under pressure by way of a tube 5 one end of which is immersed in the liquid titanium tetrachloride. A tap 6 is connected in the tube 5. The glass vessel 2 is closed by a glass plug '7 through which extends a tube 8 opening into the space above the liquid titanium tetrachloride in the vessel 2 and communicating with the interior of a cylindrical graphite die 9. A branch tube 10 connects the tube 8 to the hydrogen source 4 and a tap 11 is connected in the tube 10. The hydrogen source 4 is connected to both the tubes 5 and 10 by a common tube 12 in which there is provided a further tap 13 whereby the hydrogen source may be isolated from the rest of the system. The die 9 is heated in any suitable manner, for example, by the electric heating coil 14 shown in FIGURE 1 which is connected by way of terminals 14a to a suitable source of supply.
The water-bath 3 vaporizes the titanium tetrachloride and, with the taps 6 and 13 open and the tap 11 closed, a mixture of vaporized titanium chloride and hydrogen flows into the cavity or interior of the die 9 so that the surface of the wall thereof is exposed to this mixture. The die 9 is heated by the coil 14 to a temperature of from 1500 C.1600 C., e.g., 1550 C. and the mixture of vaporized titanium chloride and hydrogen is caused to flow through the die 9 for a period of one to two hours, e.g., one hour. The end of the die 9 remote from the tube 8 is restricted by a plug and the gases issue from this end as a jet which is ignited. During the period referred to the carbon of the die reacts with the titanium tetrachloride to form a film of titanium carbide on the internal wall of the die 9 and at the end of this period the tap 6 is closed and the tap 11 is opened so that the supply of vaporized titanium tetrachloride is discontinued and hydrogen only passes to the interior of the die 9, the latter now being heated by the coil 14 to a temperature of about 2050 C. for a short period of the order of 15 minutes and then being allowed to cool, the hydrogen atmosphere being mamtained during the cooling of the die. This high temperature heating improves the adherence of the titanium carbide to the die and removes any free titanium metal which might be present in the film by converting it to the carbide.
The procedure described above may be used to coat the interior of the die 9 with vanadium carbide by substituting vanadium tetrachloride for the titanium tetrachloride in the vessel 2.
Where the tetrachloride of the transition element is a solid which sublimes such as in the case of zirconium tetrachloride the procedure described above is modified as shown in FIGURE 2 by substituting a copper tube 15 for the vessel 2 and water bath 3. Like reference numerals are used to indicate like parts in FIGURES 1 and 2. The zirconium tetrachloride is disposed in the copper tube 15 and is heated by any suitable means such as, for example,
a tubular wire wound resistance furnace indicated very diagrammatically by the heating coil 16, to a temperature of from 250 C.300 C., e.g., 270 C. and hydrogen gas is passed through the tube 15 from the source 4 for a period of one to two hours as before and the mixture of hydrogen and zirconium tetrachloride passed into the die 9, which latter is in this case maintained at a temperature of between 1700 C. and 1900" C. During this period the Zirconium tetrachloride reacts with the carbon of the die to form zirconium carbide as a film on the interior of the die 9 and at the end of the period the tap 6 is closed and the tap 11 is opened so that hydrogen is supplied to the interior of the die 9 whilst the latter is now heated by the coil 14 to a temperature of at least 2,100 C. for a short period of the order of 15 minutes after which it is allowed to cool whilst maintaining the atmosphere of hydrogen.
The method of producing a film of the carbide of a transition element in Group VI using the carbonyl of the transition element is as follows: The die 9 (FIG. 3) is disposed in a vacuum furnace 17 the interior of which is connected by a pipe 18 through a tap 19 to a vacuum pump 20. The interior of the furnace 17 is also connected by a pipe 21 through a tap 22 to a container 23 containing the carbonyl of the transition element, e.g., molybdenum carbonyl (Mo(CO) which is a solid at normal temperature and pressure. The interior of the container 23 is connected by a pipe 24 and a tap 25 to a source 26 of hydrogen under pressure. The die 9 is heated to a temperature of about 500 C. and the tap 19 is opened and the pump 20 operated to reduce the pressure in the furnace 17 to below 0.1 mm. of mercury. The taps 22 and 25 are opened to cause a gaseous mixture of hydrogen and the carbonyl to flow into the furnace 17, the taps 19 and 22 being adjusted to control the rate of flow of this gaseous mixture and the pressure within the furnace 1'7, this pressure being maintained at about 5 mm. of mercury and the rate of flow of the gaseous mixture being about /2 litre/min. It will be understood that although the carbonyls of the transition elements in Group VI are solids at N.T.P. their vapor pressure is suflicient to provide the required quantity of gaseous carbonyl at the reduced pressure existing in the furnace 17. The gaseous mixture is allowed to flow into and through the furnace 17 for a period of at least 2 hours during which period the hydrogen reduces the carbonyl to the carbide which is deposited on the surface or surfaces of the die. After this the die 9 is cooled in a vacuum, and is subsequently removed from the furnace 17 and transferred to a high temperature furnace where it is heated to a temperature of 2000 C.2l00 C. in a protective atmosphere, e.g., hydrogen, for a period of about 15 minutes and allowed to cool whilst the protective atmosphere is maintained in order to tire the carbide film on to the surface or surfaces of the die.
In the method of applying the carbide coating to the die cavity surface or surfaces by contacting the said surface or surfaces with a slurry of the metal carbide, a mixture of finely ground carbide powder and water is first prepared. Upon agitation the fine powder will be suspended within the aqueous medium. The coating is applied by temporarily sealing the lower end of the die in such a manner as to plug the cavity or bore. The aqueous slurry is then introduced into the die cavity and agitated. The slurry may be additionally agitated prior to introduction to the die cavity in order to ensure a suitable suspension of the carbide powder. The carbide particles will come out of the slurry and adhere to the surface or surfaces of the die cavity forming the desired film. Excess water and the temporary seal or plug are removed from the die cavity and the die is then loaded with the powder to be pressed. Protective gas such as argon, nitrogen, or hydrogen is introduced to the die cavity at the beginning of the pressing operation. As the hot pressing die assembly is brought up to the temperature for hot pressing the moisture is removed, and the carbide film is subjected to a temperature of at least about 2000 C. to fire the coating onto the said surface or surfaces.
Alternatively, the contacting of the surface or surfaces of the die cavity with the aqueous-carbide mixture or slurry may be accomplished by painting or brushing the slurry on to the said surface or surfaces. Also, the desired carbide coating may be applied by first wetting the surface or surfaces of the die cavity with water in any convenient manner. Finely ground carbide powder is then dusted onto the wet surface. The so treated die is installed in the furnace, and the powder to be pressed is loaded into the die and subjected to the hot pressing operation.
The aqueous medium in these methods acts as an adhesive enabling the carbide to remain on the die until the powder to be pressed is introduced into the die. The powder when in the die suports the carbide material on the die wall and prevents it from flaking off as would occur when the aqueous mixture is dried. Thus, it is ap parent that the firing of the carbide coating can be accomplished either prior to the addition of the powder to the die or after the powder is introduced and during the hot pressing thereof.
FIGURES 4 and 5 illustrate a cylindrical graphite die 9 having a coating 27 of carbide in accordance with this invention, the thickness of this coating being exaggerated for the purpose of illustration. FIGURE 4 also shows two plungers 28 which may be hydraulically operated for the purpose of exerting a pressure on any powdered material placed in the die 9 for hot pressing to the shape of a rod.
A graphite die 9 having a carbide coating 27 in accordance with this invention is of particular, but not exclusive, application in the hot pressing of the diborides of titanium and zirconium. For example, when titanium diboride is hot pressed in a graphite die at a temperature of the order of 2000 C. there is a marked tendency for the titanium diboride to stick to the die with the result that the latter breaks before the pressing operation is completed, or the pressed body of titanium diboride breaks during cooling as a result of the differential contraction of the die and the pressed body. These difliculties are not encountered when the hot pressing operation is performed at a temperature below 1700 C. but it is not possible to produce a satisfactory strong and dense body at such low temperatures. It is thought that titanium diboride and carbon have some mutual solubility at temperatures of the order of 2000 C. or above or that the effect may be due to small amounts of impurity, such as boric oxide (B 0 which it is not economic to remove from the titanium diboride powder. Whatever the reason for the sticking effect we have found that titanium diboride may be satisfactorily hot pressed at temperatures of the order of 2000 C. and above in a graphite die when the surface or surfaces of the wall or walls defining the cavity in the die is or are coated with a film of the carbide of one of the transition elements in Groups IV, V and VI of the Periodic System, e.g., titanium carbide.
Reasonable hot pressed bodies of titanium diboride may be produced in graphite dies treated by the first method described above, i.e., by painting and firing, but it is extremely desirable, if not essential, that the painting and firing be repeated after each pressing operation.
Titanium diboride can be hot pressed at the highest temperatures normally used (about 2050 C.) in a die treated by any of the other methods described above without sticking occurring and a number of pressings (at least six) can be obtained from a given die without further treatment. As an example a powder of titanium diboride was hot-pressed in a cylindrical graphite die 9 such as illustrated in FIGURE 4 at a maximum temperature of 2050 C. and a maximum pressure of 1 ton/sq. in. on the plungers 28. The surface of the die 9 defining the cavity was coated with titanium carbide by the tetrachloride method described above. The resultant titanium diboride bar had a low porosity of the order of 6% by volume and a transverse rupture modulus of about 15 tons per sq. in. No sticking of the titanium diboride to the die 9 occurred and the surface of the die 9 defining the cavity was unimpaired and the die 9 was suitable for further operations.
The provision of a film of titanium carbide on the surface or surfaces of the wall or walls defining the die cavity is beneficial not only in the hot pressing of titanium diboride and the borides or diborides of the other transition elements in Groups IV, V and VI of the Periodic System but is also beneficial for the hot pressing of the carbides of such elements. For example, although sticking does not occur appreciably in the hot pressing of titanium carbide, the soft graphite dies do score in use and often have to be discarded for this reason alone. The treated dies, however, show no signs of scoring since the film is both hard and durable. This film is also helpful in minimizing die reaction in cases where the material being hot pressed reacts with the material of the die.
For example, oxide ceramics tend to react with the graphite of the die during pressing, but oxides are in general much less reactive towards titanium carbide.
It will be appreciated that although the invention has been specifically described with reference to producing a film of titanium carbide, vanadium carbide, zirconium carbide or molybdenum carbide on the surface or surfaces of the wall or walls of the die cavity it is not limited to the film being of one of these carbides as it is within the scope of the invention to provide such a film of a carbide of any one of the transition elements of Groups 1V, V and VI of the Periodic System, namely, titanium, zirconium and hafnium, vanadium, niobium and tantalum and chromium, molybdenum and tungsten. At present, however, titanium tetrachloride is both the cheapest and most freely available material for producing a suitable film on the surface or surfaces of the wall or Walls of the die cavity so that it is most economic to form the film from titanium carbide.
What I claim is:
1. A graphite die for use in a high temperature hot pressing process having disposed on the surfaces defining a die cavity a fired coating comprising a film of a carbide of a metal selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum and tungsten, said film containing no free metal.
2. A graphite die as in claim 1 wherein the fired coating is titanium carbide.
3. A graphite die as in claim 1 wherein the fired coating is zirconium carbide.
4. A graphite die as in claim 1 wherein the fired coating is molybdenum carbide.
5. A graphite die as in claim 1 wherein the fire coating is vanadium carbide.
References Cited by the Examiner UNITED STATES PATENTS 2,860,075 11/58 Alexander et a1. 117-228 X OTHER REFERENCES Powell: Vapor Plating (1955), Wiley, New York, pages 73-79 relied on.
RICHARD D. NEVIUS, Primary Examiner.

Claims (1)

1. A GRAPHITE DIE FOR USE IN A HIGH TEMPERATURE HOT PRESSING PROCESS HAVING DISPOSED ON THE SURFACES DEFINING A DIE CAVITY A FIRED COATING COMPRISING A FILM OF A CARBIDE OF A METAL SELECTED FROM THE GROUP CONSISTING OF TITANIUM, ZIRCONIUM, HAFNIUM, VANADIUM, NIOBIUM, TANTALUM, CHRO-
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Cited By (15)

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US3264135A (en) * 1962-11-28 1966-08-02 Noel T Wakelyn Method of coating carbonaceous base to prevent oxidation destruction and coated base
US3271181A (en) * 1963-05-29 1966-09-06 Robert A Jewell Method of coating carbonaceous base to prevent oxidation destruction and coated base
US3389743A (en) * 1965-07-12 1968-06-25 Morozov Evgeny Ilich Method of making resinous shell molds
US3416944A (en) * 1964-10-26 1968-12-17 Air Force Usa Ablative product and method for its manufactur
US3498359A (en) * 1966-03-09 1970-03-03 Imp Metal Ind Kynoch Ltd Moulds for use in metal casting
US3642522A (en) * 1969-07-15 1972-02-15 Suisse Horlogerie Rech Lab Method for producing hard coatings on a surface
US4095449A (en) * 1975-06-09 1978-06-20 The Valeron Corporation Coated punch
US4135030A (en) * 1977-12-23 1979-01-16 United Technologies Corporation Tungsten impregnated casting mold
US20090224443A1 (en) * 2008-03-05 2009-09-10 Rundquist Victor F Niobium as a protective barrier in molten metals
US20110052180A1 (en) * 2009-08-31 2011-03-03 Hon Hai Precision Industry Co., Ltd. Light blocking plate, camera module having same, and method for making same
US8574336B2 (en) 2010-04-09 2013-11-05 Southwire Company Ultrasonic degassing of molten metals
US8652397B2 (en) 2010-04-09 2014-02-18 Southwire Company Ultrasonic device with integrated gas delivery system
US9528167B2 (en) 2013-11-18 2016-12-27 Southwire Company, Llc Ultrasonic probes with gas outlets for degassing of molten metals
US10233515B1 (en) 2015-08-14 2019-03-19 Southwire Company, Llc Metal treatment station for use with ultrasonic degassing system
US11107675B2 (en) 2016-07-14 2021-08-31 Entegris, Inc. CVD Mo deposition by using MoOCl4

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US2860075A (en) * 1951-01-27 1958-11-11 Continental Can Co Method of making a heater for vacuum deposition

Patent Citations (1)

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US2860075A (en) * 1951-01-27 1958-11-11 Continental Can Co Method of making a heater for vacuum deposition

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3264135A (en) * 1962-11-28 1966-08-02 Noel T Wakelyn Method of coating carbonaceous base to prevent oxidation destruction and coated base
US3271181A (en) * 1963-05-29 1966-09-06 Robert A Jewell Method of coating carbonaceous base to prevent oxidation destruction and coated base
US3416944A (en) * 1964-10-26 1968-12-17 Air Force Usa Ablative product and method for its manufactur
US3389743A (en) * 1965-07-12 1968-06-25 Morozov Evgeny Ilich Method of making resinous shell molds
US3498359A (en) * 1966-03-09 1970-03-03 Imp Metal Ind Kynoch Ltd Moulds for use in metal casting
US3642522A (en) * 1969-07-15 1972-02-15 Suisse Horlogerie Rech Lab Method for producing hard coatings on a surface
US4095449A (en) * 1975-06-09 1978-06-20 The Valeron Corporation Coated punch
US4135030A (en) * 1977-12-23 1979-01-16 United Technologies Corporation Tungsten impregnated casting mold
CN103056318A (en) * 2008-03-05 2013-04-24 南线公司 Niobium as a protective barrier in molten metals
US9327347B2 (en) 2008-03-05 2016-05-03 Southwire Company, Llc Niobium as a protective barrier in molten metals
EP2452763A1 (en) * 2008-03-05 2012-05-16 Southwire Company Graphite die with protective niobium layer and associated die-casting method
US20090224443A1 (en) * 2008-03-05 2009-09-10 Rundquist Victor F Niobium as a protective barrier in molten metals
CN103056318B (en) * 2008-03-05 2017-06-09 南线有限责任公司 As the niobium of the protective wall in motlten metal
US8844897B2 (en) * 2008-03-05 2014-09-30 Southwire Company, Llc Niobium as a protective barrier in molten metals
US8009980B2 (en) * 2009-08-31 2011-08-30 Hon Hai Precision Industry Co., Ltd. Light blocking plate, camera module having same, and method for making same
US20110052180A1 (en) * 2009-08-31 2011-03-03 Hon Hai Precision Industry Co., Ltd. Light blocking plate, camera module having same, and method for making same
US9382598B2 (en) 2010-04-09 2016-07-05 Southwire Company, Llc Ultrasonic device with integrated gas delivery system
US8652397B2 (en) 2010-04-09 2014-02-18 Southwire Company Ultrasonic device with integrated gas delivery system
US9617617B2 (en) 2010-04-09 2017-04-11 Southwire Company, Llc Ultrasonic degassing of molten metals
US8574336B2 (en) 2010-04-09 2013-11-05 Southwire Company Ultrasonic degassing of molten metals
US10640846B2 (en) 2010-04-09 2020-05-05 Southwire Company, Llc Ultrasonic degassing of molten metals
US9528167B2 (en) 2013-11-18 2016-12-27 Southwire Company, Llc Ultrasonic probes with gas outlets for degassing of molten metals
US10316387B2 (en) 2013-11-18 2019-06-11 Southwire Company, Llc Ultrasonic probes with gas outlets for degassing of molten metals
US10233515B1 (en) 2015-08-14 2019-03-19 Southwire Company, Llc Metal treatment station for use with ultrasonic degassing system
US11107675B2 (en) 2016-07-14 2021-08-31 Entegris, Inc. CVD Mo deposition by using MoOCl4

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