US3527574A - Growth of sapphire filaments - Google Patents

Growth of sapphire filaments Download PDF

Info

Publication number
US3527574A
US3527574A US582420A US3527574DA US3527574A US 3527574 A US3527574 A US 3527574A US 582420 A US582420 A US 582420A US 3527574D A US3527574D A US 3527574DA US 3527574 A US3527574 A US 3527574A
Authority
US
United States
Prior art keywords
melt
growth
alumina
seed
filaments
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US582420A
Inventor
Harold E La Belle Jr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Saint Gobain Ceramics and Plastics Inc
Original Assignee
Tyco Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tyco Laboratories Inc filed Critical Tyco Laboratories Inc
Application granted granted Critical
Publication of US3527574A publication Critical patent/US3527574A/en
Assigned to INDIAN HEAD NATIONAL BANK reassignment INDIAN HEAD NATIONAL BANK SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SAPHIKON, INC.
Assigned to SAPHIKON, INC., A CORP. OF NEW HAMPSHIRE reassignment SAPHIKON, INC., A CORP. OF NEW HAMPSHIRE ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: TYCO LABORATORIES, INC., A CORP. OF MA.
Assigned to SAPHIKON, INC., A COMPANY OF NH reassignment SAPHIKON, INC., A COMPANY OF NH RELEASED BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: INDIAN HEAD NATIONAL BANK
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B15/00Single-crystal growth by pulling from a melt, e.g. Czochralski method
    • C30B15/20Controlling or regulating
    • C30B15/22Stabilisation or shape controlling of the molten zone near the pulled crystal; Controlling the section of the crystal
    • C30B15/24Stabilisation or shape controlling of the molten zone near the pulled crystal; Controlling the section of the crystal using mechanical means, e.g. shaping guides
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B15/00Single-crystal growth by pulling from a melt, e.g. Czochralski method
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B15/00Single-crystal growth by pulling from a melt, e.g. Czochralski method
    • C30B15/14Heating of the melt or the crystallised materials
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B15/00Single-crystal growth by pulling from a melt, e.g. Czochralski method
    • C30B15/34Edge-defined film-fed crystal-growth using dies or slits
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/16Oxides
    • C30B29/20Aluminium oxides
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S117/00Single-crystal, oriented-crystal, and epitaxy growth processes; non-coating apparatus therefor
    • Y10S117/90Apparatus characterized by composition or treatment thereof, e.g. surface finish, surface coating
    • 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
    • Y10T117/00Single-crystal, oriented-crystal, and epitaxy growth processes; non-coating apparatus therefor
    • Y10T117/10Apparatus
    • Y10T117/1024Apparatus for crystallization from liquid or supercritical state
    • Y10T117/1032Seed pulling
    • Y10T117/1036Seed pulling including solid member shaping means other than seed or product [e.g., EDFG die]

Definitions

  • refractory materials exhibit improved mechanical properties when produced in fiber or filament form and that composite materials consisting of :solid matrices reinforced by such fibers have enormous potential usefulness in the fabrication of strong heat resistant components for turbines, jet engines, missiles, rockets and other high performance equipment.
  • a number of different refractory materials have been suggested for use as a reinforcing or strengthening elements, including boron, borides, carbides, nitrides and oxides, such as SiC, Zr O B C, MgO, BeO and A1 0 a-Alumina is of particular interest because of its high melting point, high modulus of elasticity and tensile strength.
  • Another object of this invention is to grow a-alumina filaments from the melt.
  • Growth of crystalline material from an open melt customarily occurs in one of two dif ferent ways. In one case growth occurs above the surface of the melt, typically according to the Czochralski technique. In the other case growth occurs below the surface of the melt. The latter method is known as dendritic growth and occurs only in a supercooled melt. As a :seed grows down into the body of the melt, it is withdrawn at a rate sufficient to keep the growth section below the melt surface.
  • Typical of the successful prior art processes involving dendritic growth from the melt are those developed for growing silicon and germanium.
  • a more specific object is to provide a method and apparatus adapted to produce u-alumina in filaments of extended length by continuous dendritic growth from the melt.
  • a further specific object is to produce sapphire and ruby filaments by continuous dendritic growth from the melt.
  • Sapphire is pure a-alurnina in single crystal form whereas ruby is a-alumina with some of the aluminum atoms in its crystal lattice replaced by chromium.
  • a melt of tat-alumina establishing a thermal distribution within the melt conducive to dendritic propagation vertically in the melt, introducing a seed into a supercooled region of the melt for a period suflicient for dendritic growth to be initiated, and then withdrawing the seed at a rate approximately equal to the rate at which a-alumina dendrite grows downward into the melt.
  • Proper thermal distribution within the melt is achieved by novel means located on top of the melt but designed so as not to interfere with withdrawal of the seed and the a-alumina filament grown thereon.
  • FIG. 1 is an elevational sectional view, partly in schematic form, of a preferred apparatus for carrying out the process of this invention.
  • FIG. 2 is a magnified sectional view of part of the apparatus of FIG. 1.
  • a-alumina dendrites can be made to propagate vertically into the melt and that aalumina can be pulled from the melt as a continuous filament by providing a plate of selected material that floats on the surface of the melt and has an orifice through which the grown crystal can be pulled.
  • This orifice plate does not function as a die, i.e., the melt is not extruded through its orifice; instead the floating orifice plate appears to function as a heat shield in that it modifies the thermal distribution within the melt in a manner conducive to vertical rather than horizontal propagation of dendrites.
  • the illustrated apparatus comprises a vertically moveable horizontal bed 2 on which is supported a furnace enclosure consisting of two ooncentric-spaced quartz tubes 4 and 6. At its bottom end the inner tube 4 is positioned in an L-gasket 5 in the bed. Surrounding tube 4 is a sleeve '8 that screws into collar 10. Between sleeve 8 and collar 10 is an O-ring 12 and a spacer 13. The O-ring 12 is compressed against tube '4 to form a seal. The upper end of sleeve 8 is spaced from tube 4 so as to accommodate the bottom end of tube 6.
  • Tube 6 is secured in place by an O-ring 14 and a spacer 15 compressed between a collar 16 that screws onto sleeve 8.
  • Sleeve 8 is provided with an inlet port fitted with a flexible pipe 20.
  • the upper ends of tubes 4 and 6 are secured in a head 22 so that they remain stationary when the bed is lowered.
  • Head 22 has an outlet port with a flexible pipe 24.
  • head 22 includes means similar to sleeve 8, O-rings 12 and 14, and collars 10 and 16 for holding the two tubes in concentric sealed relation. Pipes and 24 are connected to a pump (not shown) that continuously circulates cooling water through the space between the two quartz tubes.
  • the interior of the furnace enclosure is connected by a pipe 28 to a vacuum pump or to a regulated source of inert gas such as argon or helium.
  • the furnace enclosure also is surrounded by an RF. heating coil 30 that is coupled to a controllable 500 kc. power supply (not shown) of conventional construction.
  • the heating coil may be moved up or down along the length of the furnace enclosure and means (not shown) are provided for supporting the coil in any selected elevation.
  • the circulating water not only keeps the inner quartz tube at a safe temperature but also absorbs most of the infrared energy and thereby makes visual observation of crystal growth more comfortable to the observer.
  • the head 22 is adapted to provide entry into the furnace enclosure of an elongate pulling rod 32 that is connected to and forms part of a conventional crystal pulling mechanism represented schematically at 34.
  • the pulling mechanism 34 is adapted to move pulling rod 32 axially and also to rotate it on its axis, both at controlled rates.
  • Pulling rod 32 is disposed coaxially with the quartz tubes 4 and 6 and its lower end has an extension in the form of a metal rod 36 that is adapted to function as a holder for a seed crystal 38.
  • a cylindrical heat susceptor 40 made of carbon.
  • the top end of susceptor 40 is open but its bottom end is closed off by an end wall.
  • the susceptor is supported on a tungsten rod 42 that is mounted in bed 2.
  • Supported within susceptor 40 on a short tungsten rod 44 is a crucible 46 adapted to contain a suitable supply of alumina 48.
  • the crucible is made of a material that will withstand the operating temperatures and will not react with or dissolve in the molten alumina. In the illustrated embodiment the crucible is made of molybdenum, but it also may be made of iridium or some other material with similar properties with respect to molten alumina.
  • the molybdenum crucible must be spaced from the susceptor since there is a eutectic reaction between carbon and molybdenum at about 2200 C.
  • the inside of the crucible is of constant diameter and may have a hemispherical bottom.
  • a cylindrical radiation shield 50 made of carbon cloth is wrapped around the carbon susceptor. The carbon cloth does not appear to couple directly to the RF. field but greatly reduces the heat loss from the carbon susceptor. At a given RF. power setting the shield 50 increases the susceptor temperature by as much as 500" C.
  • the crucible contains a heat shield in the form of an orifice plate 52 that is made of molybdenum and floats on the surface of the melt.
  • the orifice plate is made with smooth polished surfaces and preferably has a thickness in the range of 0.25 to 1 mm.
  • the plate is shaped to conform to the interior of the crucible and as shown in FIG. 2 is sized so as to provide clearance suflicient for it to float evenly on the melt and to move down in the crucible as the melt is depleted. A clearance of about 0.010 inch suffices.
  • the orifice plate has a centrally located circular orifice 54.
  • the orifice has a diameter of about inch, but equally satisfactory results have been obtained with orifices measuring & inch.
  • An orifice larger than A inch also may be used provided its crosssectional area is not so large with respect to the overall size of the plate to prevent the latter from establishing the proper thermal distribution in the melt.
  • tit-alumina seed crystal 38 is mounted in holder 36 with its C-axis aligned parallel to the holders path of movement.
  • a quantity of substantially pure a-alumina is placed in crucible 46, orifice plate 52 is placed on top of the alumina, and then the crucible is placed within susceptor 40 on tungsten rod 44.
  • Access to the seed holder and the susceptor is achieved by lowering bed 2 away from the furnace enclosure and lowering the seed holder to below the bottom end of tube 4. With the bed restored to the position of FIG.
  • cooling water is introduced between the Walls of the two quartz tubes, and the enclosure is evacuated and then filled with helium. The latter is kept at a pressure of about 1 atmosphere thereafter. Then the RF. coil is energized and operated so that the u-alumina is brought to a molten condition. It is to be noted that the orifice plate does not sink into the melt but floats at its surface, even though the plates density is greater than that of the melt. The reason for this is that the melt does not wet molybdenum.
  • the a-alumina is brought to a temperature slightly above its melting point which is in the range of 2040 to 2050 C.
  • the height of the meniscus 56 of the alumina in orifice 54 is an inverse function of the diameter of the orifice and typically is almost flush with the top surface of the orifice plate.
  • the temperature of the melt is adjusted accordingly and the seed again is brought into contact with the melt. At the proper melt temperature, dendritic growth will occur on the end of the seed. Thereafter the seed is withdrawn at a speed corresponding to the rate at which the dendrite growth propagates down into the melt. If the seed continues to be withdrawn at the proper speed, the growth will be continuous until the melt is depleted. The orifice plate will settle within the crucible as the alumnia is depleted. The maximum length has been limited only by the maximum pulling distance afforded by pulling mechanism 34.
  • the habit of thefilament-like crystals produced according to the foregoing method has shown variations that can be generalized into four different types, all of which have been grown using a sapphire seed crystal oriented with its C-axis parallel to the axis of the seed holder.
  • One habit is characterized by a rather uniform outer surface and a circular cross-section.
  • the other habits all have more or less rectangular cross-sections, but the outer surface of one has irregular undulations, another is stepped longitudinally, and the third appears to be twisted longitudinally. All of these different habits have easily discernible features.
  • the filaments appear to be single crystals, some samples show evidence of a twin morphology.
  • Laue X-ray back reflection photographs of some sample filaments reveal certain interesting facts.
  • One Laue back reflection photograph of a filament grown on a C-axis oriented sapphire seed revealed three-fold symmetry except that each reflection was split into three or four spots. This suggests the presence of three or four crystals with their C-axis approximately parallel to the filament axis but slightly misoriented with respect to each other. Other filaments give still more complex patterns but generally still with the features of three-fold symmetry.
  • a Laue back reflection of a sapphire filament grown onto a tungsten seed did not display any apparent three-fold symmetry along the filament axis.
  • a further interesting phenomenon is that the crosssectional shape and sizes of the filaments do not conform to the shape and size of the orifice through which they are pulled. This is different from what occurs in other crystal growing processes where a melt is extruded through a die.
  • the germanium ribbon pulled from the melt through a carbon die has a cross-section of the same shape and substantially the same area as the die passage exit.
  • the difference is attributable to the fact that in my process the crystal grows dendritically down into the melt, i.e., the solid/liquid interface of the fila ment is below the melt surface, while in the process of Vogel et al., the molten material solidifies within or above the die passage.
  • the orifice plate used in my process does not shape the filament, except insofar as the plate shapes the temperature gradients.
  • the filament shape appears to be affected by the temperature gradients, the average temperature of the melt, and the orientation of the seed crystal.
  • the rate of pull appears to affect the size of the filament and to some extent its shape.
  • the molybdenum orifice plate has a lower total emissivity than alumina at temperatures in the order of 2000 C. Accordingly it is believed that this property enables the floating plate to act as a heat shield which limits the heat loss from the melt surface and thereby controls the radial and longitudinal temperature gradients in the immediate vicinity of the small surface of the melt exposed within the orifice.
  • the heat shielding effect of the floating plate not only establishes the correct temperature distribution required to promote propagation vertically but also permits the melt to be supercooled in the region where the seed is introduced, an essential condition for dendritic growth.
  • the floating molybdenum plate serves the dual function of providing an effective heat shield and an exposed central growth orifice of any chosen diameter.
  • a definite indication of the fact that growth is dendritic is the speed at which the filament may be pulled from the melt.
  • I have pulled filaments at speeds up to about mm./min. using a floating plate with an orifice having a diameter of inch. This is substantially in excess of the one inch/min. speed employed in growing germanium strip crystal using the process of Vogel et al., cited above. It is believed that growth rates substantially faster than 150 mm./min. can be achieved if the heat loss from the filament (primarily radiative in the apparatus and process described above) is augmented by forced convection. It also is to be appreciated that with proper control, simultaneous growth of a plurality of filaments from a common melt may be achieved using an orifice plate with a number of orifices located so that each meniscus is at approximately the same temperature.
  • the seed crystal may also be mounted so that its C-axis is at an angle to the axis of the crystal holder.
  • a twinned seed may be used. It also is to be understood that the process need not be carried out in a helium or argon atmosphere; instead the furnace enclosure may be evacuated to a suitable level.
  • the invention has several other advantages.
  • the apparatus for producing the thermal conditions essential to dendritic growth is simple and the floating orifice plate is not restricted to use with the particular furnace design illustrated in the drawings but may be employed in other apparatus adapted to pull crystals from a melt.
  • Another advantage is that the process may be used to grow ruby filaments.
  • the most important advantage is that it provides a new and useful form of [Jr-alumina, i.e., extended filaments.
  • I have grown sapphire filaments measuring 6 inches in length and 0.13 to 0.50 mm. in diameter at pulling rates up to 150 mm./min.
  • sample sapphire filaments produced in the manner described above have been found to have an elastic modulus of 3050 10 p.s.i. (as measured by the vibrating Reed technique), a flexure modulus of 25x10 p.s.i., and a tensile strength of at least 125,000 p.s.i.
  • filament is not limited to a crystalline product of circular cross-section but also embraces polygonal cross-sections.
  • Apparatus for producing a filament of crystalline alpha-alumina comprising a furnace enclosure, a crucible in said enclosure adapted to contain a supply of alumina, means for heating said crucible to melt said alumina and hold it at a selected temperature above its melting point, said crucible including a plate with an orifice that is adapted to float on the surface of said melt and to reduce radiative heat loss from said melt so as to produce in said melt a thermal distribution conducive to crystal growth propagated vertically in a region of said melt exposed by said orifice, said crucible and plate being made of molybdenum or iridium, and means for positioning a seed crystal in said orifice so that crystal growth can occur thereon and for withdrawing said seed with its grown crystal at a rate consistent with the rate of crystal growth propagated.
  • a method of producing a filment of crystalline alphaalumina comprising providing in a crucible made of molybdenum or iridium a melt of alumina and a plate floating in said melt at the surface thereof, said plate having an aperture and being made of molybdenum or iridium, adjusting the temperature of said melt so that crystal growth propagating vertically will occur on a seed introduced into a region of said melt exposed by said aperture inserting a seed crystal into said region by way of said aperture for a period of time sufiicient for crystal growth to occur thereon, and pulling said seed upwardly away from said melt at a speed not exceeding the rate at which said crystal growth propagates vertically so that successive accretions of grown crystal form an extended filament.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Description

Sept. 8, 1970 H. E. LA BELLE, JR
GROWTH OF SAPPHIRE FILAMENTS Filed Sept. 27, 1966 PULLING MECHANISM MOL. YEDENUM 0/? INVENTOR.
HAROLD E. LABELLE JR.
ATTORNEY United States Patent 3,527,574 GROWTH OF SAPPHIRE FILAMENTS Harold E. La Belle, Jr., Billerica, Mass., assiguor to Tyco Laboratories, Inc., Waltham, Mass., a corporation of Massachusetts Filed Sept. 27, 1966, Ser. No. 582,420 Int. Cl. B01j 17/18 US. Cl. 23--273 12 Claims ABSTRACT OF THE DISCLOSURE This invention relates to production of filaments of refractory materials and more particularly to filaments of a-alumina.
This invention is related to the inventions disclosed and claimed in the following co-pending applications of Abraham I. Mlavsky and Harold E. La Belle, Jr.: Ser. No. 621,731, filed Feb. 14, 1967, now abandoned, for Method And Apparatus For Growing Inorganic Filaments; and Ser. No. 666,304, filed Sept. 8, 1967, for Method And Apparatus For Growing Inorganic Filaments, Ribbon From The Melt.
It is recognized that certain refractory materials exhibit improved mechanical properties when produced in fiber or filament form and that composite materials consisting of :solid matrices reinforced by such fibers have enormous potential usefulness in the fabrication of strong heat resistant components for turbines, jet engines, missiles, rockets and other high performance equipment. A number of different refractory materials have been suggested for use as a reinforcing or strengthening elements, including boron, borides, carbides, nitrides and oxides, such as SiC, Zr O B C, MgO, BeO and A1 0 a-Alumina is of particular interest because of its high melting point, high modulus of elasticity and tensile strength. However, while various methods have been developed for growing single crystal fibers of a-alumina, the fibers are almost always of short length and small diameter, typically no longer than 6-7 mm. long and 0.01 mm. thickness. Attempts to produce longer fibers have been fruitless or only partially successful and it has not been possible to grow extended filaments. While small single crystal fibers (also called whiskers) exhibit very large tensile strengths and, therefore, have utility as reinforcing elements in composite materials, they are difficult to handle.
Accordingly it is an object of this invention to provide m-alumina in extended filament form.
Another object of this invention is to grow a-alumina filaments from the melt. Growth of crystalline material from an open melt customarily occurs in one of two dif ferent ways. In one case growth occurs above the surface of the melt, typically according to the Czochralski technique. In the other case growth occurs below the surface of the melt. The latter method is known as dendritic growth and occurs only in a supercooled melt. As a :seed grows down into the body of the melt, it is withdrawn at a rate sufficient to keep the growth section below the melt surface. Typical of the successful prior art processes involving dendritic growth from the melt are those developed for growing silicon and germanium.
Patented Sept. 8, 1970 "ice Each of these materials is characterized by a discrete twin morphology so that dendritic growth is easily possible. So-called web silicon used in semiconductor applications is sheet silicon pulled from the melt as the connecting member between two parallel dendrites. Relatively few other crystalline materials have been grown dendritically from the melt in extended ribbon or filament form.
Accordingly it is a further object of this invention to apply the concept of dendritic growth to produce aalumina in extended filament form from the melt.
A more specific object is to provide a method and apparatus adapted to produce u-alumina in filaments of extended length by continuous dendritic growth from the melt.
A further specific object is to produce sapphire and ruby filaments by continuous dendritic growth from the melt. Sapphire is pure a-alurnina in single crystal form whereas ruby is a-alumina with some of the aluminum atoms in its crystal lattice replaced by chromium.
The foregoing and other objects are attained by providing a melt of tat-alumina, establishing a thermal distribution within the melt conducive to dendritic propagation vertically in the melt, introducing a seed into a supercooled region of the melt for a period suflicient for dendritic growth to be initiated, and then withdrawing the seed at a rate approximately equal to the rate at which a-alumina dendrite grows downward into the melt. Proper thermal distribution within the melt is achieved by novel means located on top of the melt but designed so as not to interfere with withdrawal of the seed and the a-alumina filament grown thereon.
Objects and many of the attendant advantages of my invention are believed to be apparent from the following detailed description which is to be considered together with the accompanying drawings, wherein:
FIG. 1 is an elevational sectional view, partly in schematic form, of a preferred apparatus for carrying out the process of this invention; and
FIG. 2 is a magnified sectional view of part of the apparatus of FIG. 1.
Experiments have demonstrated that from an open melt, a-alumina tends to grow circumferentially, i.e., radially from the seed, rather than propagate down into the melt. Dendritic growth when it occurs is parallel to the surface of the melt and often is characterized by branching of the dendrites. Variations in pulling speed do not change the direction of dendritic propagation. Further experiments have indicated that the thermal distribution within the melt is an extremely important parameter affecting continuous dendrite propagation in a vertical direction.
I have discovered that a-alumina dendrites can be made to propagate vertically into the melt and that aalumina can be pulled from the melt as a continuous filament by providing a plate of selected material that floats on the surface of the melt and has an orifice through which the grown crystal can be pulled. This orifice plate does not function as a die, i.e., the melt is not extruded through its orifice; instead the floating orifice plate appears to function as a heat shield in that it modifies the thermal distribution within the melt in a manner conducive to vertical rather than horizontal propagation of dendrites.
Referring now to FIG. 1, the illustrated apparatus provided in accordance with thhe present invention comprises a vertically moveable horizontal bed 2 on which is supported a furnace enclosure consisting of two ooncentric-spaced quartz tubes 4 and 6. At its bottom end the inner tube 4 is positioned in an L-gasket 5 in the bed. Surrounding tube 4 is a sleeve '8 that screws into collar 10. Between sleeve 8 and collar 10 is an O-ring 12 and a spacer 13. The O-ring 12 is compressed against tube '4 to form a seal. The upper end of sleeve 8 is spaced from tube 4 so as to accommodate the bottom end of tube 6. The bottom end of tube 6 is secured in place by an O-ring 14 and a spacer 15 compressed between a collar 16 that screws onto sleeve 8. Sleeve 8 is provided with an inlet port fitted with a flexible pipe 20. The upper ends of tubes 4 and 6 are secured in a head 22 so that they remain stationary when the bed is lowered. Head 22 has an outlet port with a flexible pipe 24. Although not shown, it is to be understood that head 22 includes means similar to sleeve 8, O- rings 12 and 14, and collars 10 and 16 for holding the two tubes in concentric sealed relation. Pipes and 24 are connected to a pump (not shown) that continuously circulates cooling water through the space between the two quartz tubes. The interior of the furnace enclosure is connected by a pipe 28 to a vacuum pump or to a regulated source of inert gas such as argon or helium. The furnace enclosure also is surrounded by an RF. heating coil 30 that is coupled to a controllable 500 kc. power supply (not shown) of conventional construction. The heating coil may be moved up or down along the length of the furnace enclosure and means (not shown) are provided for supporting the coil in any selected elevation. At this point it is to be noted that the circulating water not only keeps the inner quartz tube at a safe temperature but also absorbs most of the infrared energy and thereby makes visual observation of crystal growth more comfortable to the observer.
The head 22 is adapted to provide entry into the furnace enclosure of an elongate pulling rod 32 that is connected to and forms part of a conventional crystal pulling mechanism represented schematically at 34. Although not described in detail it is to be understood that the pulling mechanism 34 is adapted to move pulling rod 32 axially and also to rotate it on its axis, both at controlled rates. Pulling rod 32 is disposed coaxially with the quartz tubes 4 and 6 and its lower end has an extension in the form of a metal rod 36 that is adapted to function as a holder for a seed crystal 38.
Located within the furnace enclosure is a cylindrical heat susceptor 40 made of carbon. The top end of susceptor 40 is open but its bottom end is closed off by an end wall. The susceptor is supported on a tungsten rod 42 that is mounted in bed 2. Supported within susceptor 40 on a short tungsten rod 44 is a crucible 46 adapted to contain a suitable supply of alumina 48. The crucible is made of a material that will withstand the operating temperatures and will not react with or dissolve in the molten alumina. In the illustrated embodiment the crucible is made of molybdenum, but it also may be made of iridium or some other material with similar properties with respect to molten alumina. The molybdenum crucible must be spaced from the susceptor since there is a eutectic reaction between carbon and molybdenum at about 2200 C. The inside of the crucible is of constant diameter and may have a hemispherical bottom. In order to obtain the high operating temperatures necessary for the process, a cylindrical radiation shield 50 made of carbon cloth is wrapped around the carbon susceptor. The carbon cloth does not appear to couple directly to the RF. field but greatly reduces the heat loss from the carbon susceptor. At a given RF. power setting the shield 50 increases the susceptor temperature by as much as 500" C.
In addition to the supply of alumina, the crucible contains a heat shield in the form of an orifice plate 52 that is made of molybdenum and floats on the surface of the melt. The orifice plate is made with smooth polished surfaces and preferably has a thickness in the range of 0.25 to 1 mm. The plate is shaped to conform to the interior of the crucible and as shown in FIG. 2 is sized so as to provide clearance suflicient for it to float evenly on the melt and to move down in the crucible as the melt is depleted. A clearance of about 0.010 inch suffices. As illustrated in FIG. 2, the orifice plate has a centrally located circular orifice 54. Preferably the orifice has a diameter of about inch, but equally satisfactory results have been obtained with orifices measuring & inch. An orifice larger than A inch also may be used provided its crosssectional area is not so large with respect to the overall size of the plate to prevent the latter from establishing the proper thermal distribution in the melt.
The effect of the orifice plate on the growth process is confirmed by experiments to propagate A1 0 filaments continuously using the apparatus of FIG. 1 in the manner described below but with the plate omitted from the crucible. In these experiments a mass of alumina was melted, slowly cooled until solidification proceeded (this is to establish the melting point), remelted, and slowly cooled again to within a few degrees above the melting point. A seed with its C-axis parallel to the axis of the crystal holder was then inserted into the melt and rapidly withdrawn at a predetermined rate. These experiments succeeded in propagating dendrites parallel to the surface of the melt but failed to grow any dendrites down into the melt. This propagation behavior suggested an improper thermal distribution within the melt. Accordingly additional experiments were conducted using the same procedure but supplying more heat to the bottom of the crucible (relative to its sides). This was achieved by shifting the relative positions of the susceptor and the RP. coil. These additional experiments succeeded in dendritic growth clearly propagated vertically into the melt, but the propagation was not continuous. Dendrites grown in this manner always grew downward from a much larger mass of solidified lit-A1203, and would stop growing vertically as the larger mass was withdrawn. This behavior suggested that although the increased heat applied to the bottom of the crucible appeared to improve the thermal distribution within the melt enough to promote vertical dendritic growth, removal of the larger mass of solidified a-alumina from the melt caused a thermal fluctuation sufficiently larger to prevent further vertical propagation.
Introduction of the orifice plate onto the surface of the melt solved the problem of continuous growth of aalumina and confirmed that in order to obtain continuous dendritic propagation vertically into the melt, it is necessary not only to establish a critical thermal distribution but also to maintain this distribution as the dendrite is withdrawn from the melt.
Operation of the above-described apparatus and an example of the method of growing u-alumina filaments according to my invention will now be described. An tit-alumina seed crystal 38 is mounted in holder 36 with its C-axis aligned parallel to the holders path of movement. At the same time a quantity of substantially pure a-alumina is placed in crucible 46, orifice plate 52 is placed on top of the alumina, and then the crucible is placed within susceptor 40 on tungsten rod 44. Access to the seed holder and the susceptor is achieved by lowering bed 2 away from the furnace enclosure and lowering the seed holder to below the bottom end of tube 4. With the bed restored to the position of FIG. 1, cooling water is introduced between the Walls of the two quartz tubes, and the enclosure is evacuated and then filled with helium. The latter is kept at a pressure of about 1 atmosphere thereafter. Then the RF. coil is energized and operated so that the u-alumina is brought to a molten condition. It is to be noted that the orifice plate does not sink into the melt but floats at its surface, even though the plates density is greater than that of the melt. The reason for this is that the melt does not wet molybdenum. The a-alumina is brought to a temperature slightly above its melting point which is in the range of 2040 to 2050 C. In this molten condition the height of the meniscus 56 of the alumina in orifice 54 is an inverse function of the diameter of the orifice and typically is almost flush with the top surface of the orifice plate. Once temperature equilibrium is established, the pulling mechanism is actuated and operated so as to bring the seed crystal 38 into contact with the meniscus. Almost immediately thereafter the pulling mechanism is operated so as to pull the crystal at a predetermined rate of speed. The melt temperature is critical and in the usual case initial withdrawal of the seed is unaccompanied by continuous growth. At this point it is to be appreciated that if the surface of the melt is too cold, nothing will happen when the seed touches the meniscus; on the other hand, if the surface of the melt is too hot, the seed will melt. The temperature of the melt is adjusted accordingly and the seed again is brought into contact with the melt. At the proper melt temperature, dendritic growth will occur on the end of the seed. Thereafter the seed is withdrawn at a speed corresponding to the rate at which the dendrite growth propagates down into the melt. If the seed continues to be withdrawn at the proper speed, the growth will be continuous until the melt is depleted. The orifice plate will settle within the crucible as the alumnia is depleted. The maximum length has been limited only by the maximum pulling distance afforded by pulling mechanism 34.
The habit of thefilament-like crystals produced according to the foregoing method has shown variations that can be generalized into four different types, all of which have been grown using a sapphire seed crystal oriented with its C-axis parallel to the axis of the seed holder. One habit is characterized by a rather uniform outer surface and a circular cross-section. The other habits all have more or less rectangular cross-sections, but the outer surface of one has irregular undulations, another is stepped longitudinally, and the third appears to be twisted longitudinally. All of these different habits have easily discernible features. Although the filaments appear to be single crystals, some samples show evidence of a twin morphology. Thus those filaments that appear to be twisted longitudinally may in fact be twinned since the crystal ends often are characterized by two discrete points. In this connection reference is had to Dana, System of Minerology, 7 ed., p. 522, John Wiley & Sons, Inc., 1963, which discloses that walumina (also known as corundum) belongs to the hexagonal group and forms a lamella structure in the (1011) plane and also a less common twin on (0001). An additional feature is that it is subject to pressure twinning, i.e., twinning can be caused in a seed crystal by application of appropriate shear pressure.
After a particular habit has been nucleated and propagated, it is possible to separate the grown filament from the melt by fast retraction, reinsert it into the melt and then resume normal growth procedure. The dendrite filament that grows afterward will be the same crystal type as that originally propagated before separation from the melt. Laue X-ray back reflection photographs of some sample filaments reveal certain interesting facts. One Laue back reflection photograph of a filament grown on a C-axis oriented sapphire seed revealed three-fold symmetry except that each reflection was split into three or four spots. This suggests the presence of three or four crystals with their C-axis approximately parallel to the filament axis but slightly misoriented with respect to each other. Other filaments give still more complex patterns but generally still with the features of three-fold symmetry. By contrast a Laue back reflection of a sapphire filament grown onto a tungsten seed did not display any apparent three-fold symmetry along the filament axis.
A further interesting phenomenon is that the crosssectional shape and sizes of the filaments do not conform to the shape and size of the orifice through which they are pulled. This is different from what occurs in other crystal growing processes where a melt is extruded through a die. Thus, for example, in the process disclosed in U.S. Pat. No. 3,124,489, issured Mar. 10, '1964, to F. F. Vogel, Jr. et al., for Method of Continuously Growing Thin Strip Crystals, the germanium ribbon pulled from the melt through a carbon die has a cross-section of the same shape and substantially the same area as the die passage exit. The difference is attributable to the fact that in my process the crystal grows dendritically down into the melt, i.e., the solid/liquid interface of the fila ment is below the melt surface, while in the process of Vogel et al., the molten material solidifies within or above the die passage. The orifice plate used in my process does not shape the filament, except insofar as the plate shapes the temperature gradients. The filament shape appears to be affected by the temperature gradients, the average temperature of the melt, and the orientation of the seed crystal. The rate of pull appears to affect the size of the filament and to some extent its shape.
In this connection it appears from observation that the molybdenum orifice plate has a lower total emissivity than alumina at temperatures in the order of 2000 C. Accordingly it is believed that this property enables the floating plate to act as a heat shield which limits the heat loss from the melt surface and thereby controls the radial and longitudinal temperature gradients in the immediate vicinity of the small surface of the melt exposed within the orifice. The heat shielding effect of the floating plate not only establishes the correct temperature distribution required to promote propagation vertically but also permits the melt to be supercooled in the region where the seed is introduced, an essential condition for dendritic growth. In summary the floating molybdenum plate serves the dual function of providing an effective heat shield and an exposed central growth orifice of any chosen diameter.
A definite indication of the fact that growth is dendritic is the speed at which the filament may be pulled from the melt. In practice I have pulled filaments at speeds up to about mm./min. using a floating plate with an orifice having a diameter of inch. This is substantially in excess of the one inch/min. speed employed in growing germanium strip crystal using the process of Vogel et al., cited above. It is believed that growth rates substantially faster than 150 mm./min. can be achieved if the heat loss from the filament (primarily radiative in the apparatus and process described above) is augmented by forced convection. It also is to be appreciated that with proper control, simultaneous growth of a plurality of filaments from a common melt may be achieved using an orifice plate with a number of orifices located so that each meniscus is at approximately the same temperature.
Although I prefer to mount the seed crystal so that growth occurs along its C-axis OO01 it may also be mounted so that its C-axis is at an angle to the axis of the crystal holder. Moreover a twinned seed may be used. It also is to be understood that the process need not be carried out in a helium or argon atmosphere; instead the furnace enclosure may be evacuated to a suitable level.
In addition to the fact that it permits growth of alumina in filament form, the invention has several other advantages. For one thing the apparatus for producing the thermal conditions essential to dendritic growth is simple and the floating orifice plate is not restricted to use with the particular furnace design illustrated in the drawings but may be employed in other apparatus adapted to pull crystals from a melt. Another advantage is that the process may be used to grow ruby filaments. Perhaps the most important advantage is that it provides a new and useful form of [Jr-alumina, i.e., extended filaments. In this connection it is to be noted that I have grown sapphire filaments measuring 6 inches in length and 0.13 to 0.50 mm. in diameter at pulling rates up to 150 mm./min. It is to be appreciated that the length of these filaments was not limited by the process per se but only by the capability of pulling mechanism 34, and production of filaments with lengths in the order of tens of feet and higher is contingent only upon provision of apparatus of greater pulling capacity. Sample sapphire filaments produced in the manner described above have been found to have an elastic modulus of 3050 10 p.s.i. (as measured by the vibrating Reed technique), a flexure modulus of 25x10 p.s.i., and a tensile strength of at least 125,000 p.s.i.
As used herein the term filament is not limited to a crystalline product of circular cross-section but also embraces polygonal cross-sections.
It is to be understood that the invention is not limited in its application to the details of construction and arrangement of parts specifically described or illustrated, and that within the scope of the appended claims, it may be practiced otherwise than as specifically described or illustrated.
I claim:
1. Apparatus for producing a filament of crystalline alpha-alumina comprising a furnace enclosure, a crucible in said enclosure adapted to contain a supply of alumina, means for heating said crucible to melt said alumina and hold it at a selected temperature above its melting point, said crucible including a plate with an orifice that is adapted to float on the surface of said melt and to reduce radiative heat loss from said melt so as to produce in said melt a thermal distribution conducive to crystal growth propagated vertically in a region of said melt exposed by said orifice, said crucible and plate being made of molybdenum or iridium, and means for positioning a seed crystal in said orifice so that crystal growth can occur thereon and for withdrawing said seed with its grown crystal at a rate consistent with the rate of crystal growth propagated.
2. Apparatus as defined by claim 1 wherein said crucible is made of molybdenum.
3. Apparatus as defined by claim 2 wherein said plate is made of molybdenum.
4. Apparatus as defined by claim 1 wherein said crucible is made of iridium.
5. Apparatus as defined by claim 1 wherein said plate is made of iridium.
6. A method of producing a filment of crystalline alphaalumina comprising providing in a crucible made of molybdenum or iridium a melt of alumina and a plate floating in said melt at the surface thereof, said plate having an aperture and being made of molybdenum or iridium, adjusting the temperature of said melt so that crystal growth propagating vertically will occur on a seed introduced into a region of said melt exposed by said aperture inserting a seed crystal into said region by way of said aperture for a period of time sufiicient for crystal growth to occur thereon, and pulling said seed upwardly away from said melt at a speed not exceeding the rate at which said crystal growth propagates vertically so that successive accretions of grown crystal form an extended filament.
7. Method of claim 6 wherein said crucible is made of molybdenum.
8. Method of claim 7 wherein said plate is made of molybdenum.
9. Method of claim 6 wherein said crucible is made of iridium.
10. Method of claim 6 wherein said plate made of iridium.
11. Method of claim 6 wherein said seed is withdrawn at a speed in the order of mm./min.
12. Method of claim 6 wherein said seed is a single crystal having a C-axis and is oriented so that said C-axis extends substantially vertically.
References Cited UNITED STATES PATENTS 3,002,82A 10/ 1961 Francois. 3,124,489 3/1964 Vogel et al. 3,224,840 12/ 1965 Lefever. 3,291,571 12/ 1966 Dohmen et a1. 3,291,574 12/1966 Pierson. 3,291,650 12/1966 Dohmen et al. 3,298,795 1/ 1967 Hamilton.
FOREIGN PATENTS 1,293,744 5/1961 France.
NORMAN YUDKOFF, Primary Examiner C. P. RIBANDO, Assistant Examiner U.S. C1. X.R. 23-30l, 305
US582420A 1966-09-27 1966-09-27 Growth of sapphire filaments Expired - Lifetime US3527574A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US58242066A 1966-09-27 1966-09-27

Publications (1)

Publication Number Publication Date
US3527574A true US3527574A (en) 1970-09-08

Family

ID=24329079

Family Applications (1)

Application Number Title Priority Date Filing Date
US582420A Expired - Lifetime US3527574A (en) 1966-09-27 1966-09-27 Growth of sapphire filaments

Country Status (1)

Country Link
US (1) US3527574A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3655415A (en) * 1968-12-31 1972-04-11 Union Carbide Corp Asteriated synthetic corundum gem stones and method and apparatus for their production
US3939003A (en) * 1972-09-07 1976-02-17 The United States Of America As Represented By The Secretary Of The Army Fabrication of metal-ceramic composites
US4025386A (en) * 1974-12-20 1977-05-24 Union Carbide Corporation Method for producing r-plane single crystal alpha alumina in massive form having substantially circular cross-section
US4096025A (en) * 1974-02-21 1978-06-20 The United States Of America As Represented By The Secretary Of The Army Method of orienting seed crystals in a melt, and product obtained thereby
US4224099A (en) * 1978-08-10 1980-09-23 Union Carbide Corporation Method for producing R-plane single crystal alpha alumina
US4286025A (en) * 1979-03-12 1981-08-25 Grant Zigurd A Detector for thermoluminescence dosimetry
US5114528A (en) * 1990-08-07 1992-05-19 Wisconsin Alumni Research Foundation Edge-defined contact heater apparatus and method for floating zone crystal growth
US5370078A (en) * 1992-12-01 1994-12-06 Wisconsin Alumni Research Foundation Method and apparatus for crystal growth with shape and segregation control
US5458083A (en) * 1992-05-29 1995-10-17 Chichibu Cement Co., Ltd. Growth method for a rod form of single oxide crystal
US20070056508A1 (en) * 2003-04-23 2007-03-15 Tsuguo Fukuda Apparatus for producing fluoride crystal

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3002824A (en) * 1956-11-28 1961-10-03 Philips Corp Method and apparatus for the manufacture of crystalline semiconductors
FR1293744A (en) * 1961-05-24 1962-05-18 Western Electric Co Process for the growth of single crystals of corundum and gallium oxide
US3124489A (en) * 1960-05-02 1964-03-10 Method of continuously growing thin strip crystals
US3224840A (en) * 1962-11-16 1965-12-21 Gen Telephone & Elect Methods and apparatus for producing crystalline materials
US3291650A (en) * 1963-12-23 1966-12-13 Gen Motors Corp Control of crystal size
US3291571A (en) * 1963-12-23 1966-12-13 Gen Motors Corp Crystal growth
US3291574A (en) * 1963-12-23 1966-12-13 Gen Motors Corp Semiconductor crystal growth from a domical projection
US3298795A (en) * 1964-03-23 1967-01-17 Westinghouse Electric Corp Process for controlling dendritic crystal growth

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3002824A (en) * 1956-11-28 1961-10-03 Philips Corp Method and apparatus for the manufacture of crystalline semiconductors
US3124489A (en) * 1960-05-02 1964-03-10 Method of continuously growing thin strip crystals
FR1293744A (en) * 1961-05-24 1962-05-18 Western Electric Co Process for the growth of single crystals of corundum and gallium oxide
US3224840A (en) * 1962-11-16 1965-12-21 Gen Telephone & Elect Methods and apparatus for producing crystalline materials
US3291650A (en) * 1963-12-23 1966-12-13 Gen Motors Corp Control of crystal size
US3291571A (en) * 1963-12-23 1966-12-13 Gen Motors Corp Crystal growth
US3291574A (en) * 1963-12-23 1966-12-13 Gen Motors Corp Semiconductor crystal growth from a domical projection
US3298795A (en) * 1964-03-23 1967-01-17 Westinghouse Electric Corp Process for controlling dendritic crystal growth

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3655415A (en) * 1968-12-31 1972-04-11 Union Carbide Corp Asteriated synthetic corundum gem stones and method and apparatus for their production
US3939003A (en) * 1972-09-07 1976-02-17 The United States Of America As Represented By The Secretary Of The Army Fabrication of metal-ceramic composites
US4096025A (en) * 1974-02-21 1978-06-20 The United States Of America As Represented By The Secretary Of The Army Method of orienting seed crystals in a melt, and product obtained thereby
US4025386A (en) * 1974-12-20 1977-05-24 Union Carbide Corporation Method for producing r-plane single crystal alpha alumina in massive form having substantially circular cross-section
US4224099A (en) * 1978-08-10 1980-09-23 Union Carbide Corporation Method for producing R-plane single crystal alpha alumina
US4286025A (en) * 1979-03-12 1981-08-25 Grant Zigurd A Detector for thermoluminescence dosimetry
US5114528A (en) * 1990-08-07 1992-05-19 Wisconsin Alumni Research Foundation Edge-defined contact heater apparatus and method for floating zone crystal growth
US5458083A (en) * 1992-05-29 1995-10-17 Chichibu Cement Co., Ltd. Growth method for a rod form of single oxide crystal
US5370078A (en) * 1992-12-01 1994-12-06 Wisconsin Alumni Research Foundation Method and apparatus for crystal growth with shape and segregation control
US20070056508A1 (en) * 2003-04-23 2007-03-15 Tsuguo Fukuda Apparatus for producing fluoride crystal
US20110000423A1 (en) * 2003-04-23 2011-01-06 Stella Chemifa Corporation Method for producing fluoride crystal
US8333838B2 (en) 2003-04-23 2012-12-18 Stella Chemifa Corporation Method for producing fluoride crystal

Similar Documents

Publication Publication Date Title
US3471266A (en) Growth of inorganic filaments
US3650703A (en) Method and apparatus for growing inorganic filaments, ribbon from the melt
US3591348A (en) Method of growing crystalline materials
LaBelle Jr et al. Growth of controlled profile crystals from the melt: Part I-Sapphire filaments
LaBelle Jr EFG, the invention and application to sapphire growth
Rudolph et al. Fiber crystal growth from the melt
US3608050A (en) Production of single crystal sapphire by carefully controlled cooling from a melt of alumina
Dash Growth of silicon crystals free from dislocations
US4329195A (en) Lateral pulling growth of crystal ribbons
US3265469A (en) Crystal growing apparatus
US3527574A (en) Growth of sapphire filaments
Bleay et al. The growth of single crystals of some organic compounds by the Czochralski technique and the assessment of their perfection
US3031275A (en) Process for growing single crystals
US3453352A (en) Method and apparatus for producing crystalline semiconductor ribbon
Pollock Filamentary sapphire: Part 1 Growth and microstructural characterisation
US3701636A (en) Crystal growing apparatus
US3870477A (en) Optical control of crystal growth
GB1572355A (en) Silicon crystal growing
EP0141495B1 (en) A method for pulling a single crystal
US4565600A (en) Processes for the continuous preparation of single crystals
JPH04231338A (en) Stretching of slender glass article and its device
US3977934A (en) Silicon manufacture
US5879449A (en) Crystal growth
EP0144512A1 (en) Semiconductor boule pulling rod
Sworn et al. The growth of dislocation-free copper crystals

Legal Events

Date Code Title Description
AS Assignment

Owner name: INDIAN HEAD NATIONAL BANK, NEW HAMPSHIRE

Free format text: SECURITY INTEREST;ASSIGNOR:SAPHIKON, INC.;REEL/FRAME:004637/0019

Effective date: 19860530

Owner name: INDIAN HEAD NATIONAL BANK, ONE INDIAN HEAD PLAZA,

Free format text: SECURITY INTEREST;ASSIGNOR:SAPHIKON, INC.;REEL/FRAME:004637/0019

Effective date: 19860530

AS Assignment

Owner name: SAPHIKON, INC., A CORP. OF NEW HAMPSHIRE, NEW HAMP

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:TYCO LABORATORIES, INC., A CORP. OF MA.;REEL/FRAME:004634/0027

Effective date: 19860530

Owner name: SAPHIKON, INC., 51 POWERS STREET, MILFORD, NEW HAM

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:TYCO LABORATORIES, INC., A CORP. OF MA.;REEL/FRAME:004634/0027

Effective date: 19860530

AS Assignment

Owner name: SAPHIKON, INC., A COMPANY OF NH,NEW HAMPSHIRE

Free format text: RELEASED BY SECURED PARTY;ASSIGNOR:INDIAN HEAD NATIONAL BANK;REEL/FRAME:004702/0047

Effective date: 19870327

Owner name: SAPHIKON, INC., 51 POWERS STREET, MILFORD, HILLSBO

Free format text: RELEASED BY SECURED PARTY;ASSIGNOR:INDIAN HEAD NATIONAL BANK;REEL/FRAME:004702/0047

Effective date: 19870327