Adhesive Composition and Method to Join Non-Oxide Silicon Based Ceramic Parts

• US 20150247077A1
• Filed: 07/14/2014
• Published: 09/03/2015
• Est. Priority Date: 01/26/2011
• Status: Abandoned Application

• Current Assignee: Thor Technologies, Inc. (Oracle Corporation)
• Original Assignee: Thor Technologies, Inc. (Oracle Corporation)
• Inventors: Kepley, Larry J., Jacobsen, George M.
• Application Number:
  US14/331,121
• Publication Number:
  US 20150247077A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: C08G 77/60 in which all the silicon atoms are connected by linkages other than oxygen atoms
• CPC Class Codes: C08G 77/62 Nitrogen atoms
• CPC Class Codes: C08K 3/10 Metal compounds
• CPC Class Codes: C08K 3/38 Boron-containing compounds
• CPC Class Codes: C09D 183/14 in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms C09D183/10 takes precedence
• CPC Class Codes: C09D 183/16 in which all the silicon atoms are connected by linkages other than oxygen atoms
• CPC Class Codes: C09J 183/14 in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms C09J183/10 takes precedence
• CPC Class Codes: C09J 183/16 in which all the silicon atoms are connected by linkages other than oxygen atoms

Abstract

The present invention comprises an adhesive composition and a method of using the composition to join non-oxide, silicon-based ceramic parts. The composition is a non-aqueous paste comprising high levels of non-oxide powders, silicon carbide or silicon nitride powder blended with a mixture of polymeric precursors to silicon carbide and zirconium boride. The resulting blend of the present invention is capable of decomposing on heating (in an inert or reducing atmosphere) into Si-based ceramic phases. The powder is fully suspended and dispersed in the polymer such that pockets of dry powder are not present. Although the polymer penetrates between particles and wets the surfaces to be joined, it does not prevent some contact between particles and the surface. Because the paste contains only low levels of volatile solvents and it converts into Si-based ceramics upon pyrolysis, it provides strong chemical bonding to Si-based ceramics.

Claims

1. A nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance, the composition comprising a uniformly-mixed and blended mixture of:

a. a liquid polymer precursor to a transition metal boride ceramic phase MB_x wherein M is selected from the group consisting of Zr and Hf, and x ranges from 1 to 2, the precursor comprising a polymeric composition represented by the formula [MB_xH_y]_n wherein x is in the range 1 to 2, y ranges from 0 to 9 and n is a least 4, the precursor being capable of being converted into an amorphous or microcrystalline ceramic phase by being heated in an atmosphere selected from the group consisting of inert, reducing and vacuum, the precursor being derived from reacting an amine with M(BH₄)₄, where M is Zr or Hf, the precursor being present in the range 5% to 62% by weight of the composition;

b. a polymeric precursor to silicon carbide-based ceramic phase selected from the group consisting of a polysilazane and a polycarbosilane, the precursor being capable of mixing with the MB_x precursor, the precursor being present in the range 5% to 62% by weight of the composition; and

c. a non-oxide ceramic powder having a grain size of less than 5 μ

m, the powder being selected from the group consisting of silicon nitride and silicon carbide, the powder blending with and suspending in the ceramic precursors at a level in the range 33% to 80% by weight of the composition without sieving the mixture, with the non-oxide ceramic powder to polymeric precursor ratio ranging from 0.5;

1 to 4;

1.

2. The nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance of claim 1 wherein heat treatment yields ZrB_x ceramic phases with domain sizes less than 0.5 μ

m.

3. The nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance of claim 1 wherein the paste is capable of being used to infiltrate and modify porous materials, the porous materials selected from the group consisting of powder compacts, wood, minerals, ceramic matrix composites, graphite, carbon foams, ceramic materials, metallic foams, textiles and paper.

4. The nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance of claim 1 wherein the paste is capable of being used as a high temperature adhesive, as a precursor to ceramic coatings, as a sealant or coating of silicon, ceramic matrix composites, or ceramic materials, including packages of electronic components or microelectronic machined micromechanical devices (MEMs), as sealant or coating of nuclear fuel rods, or as a material for fabrication of ceramic materials and composites, such as by extrusion or molding of ceramic parts or materials.

5. The nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance of claim 1 wherein the paste is capable of being used for sealing of, bonding to, or joining of ceramic, ceramic composite, metallic, or carbon-based materials, parts, sensors, electronics, or feed-throughs, and to protect the integrity of those materials.

6. The nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance of claim 1 wherein the paste is capable of being used to form ceramic coatings for high-temperature thermal protection, oxidation resistance, wear resistance, printing, jewelry, heating elements, ceramic matrix composites, glow plugs, gas-turbine components, filters, catalyst supports, glasses, armor, combustion chambers, prosthesis, or decorative coatings.

7. A nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance, the composition comprising a uniformly-mixed and blended mixture of:

a. a liquid polymer precursor to a transition metal boride ceramic phase MB_x wherein M is selected from the group consisting of Zr and Hf, and x ranges from 1 to 2, the precursor comprising a polymeric composition represented by the formula [MB_xH_y]_n wherein x is in the range 1 to 2, y ranges from 0 to 9 and n is a least 4, the precursor being capable of being converted into an amorphous or microcrystalline ceramic phase by being heated in an atmosphere selected from the group consisting of inert, reducing and vacuum, the precursor being derived from reacting an amine with M(BH₄)₄, where M is Zr or Hf, the precursor being present in the range 5% to 62% by weight of the composition;

b. a polymeric precursor to silicon carbide-based ceramic phase selected from the group consisting of a polysilazane and a polycarbosilane, the precursor being capable of mixing with the MB_x precursor, the precursor being present in the range 5% to 62% by weight of the composition; and

c. a non-oxide ceramic powder having a grain size of less than 5 μ

m, the powder being selected from the group consisting of silicon nitride and silicon carbide, the powder being doped less than 5% by weight with powder selected from the group consisting of lithium, aluminum hydride, zirconium hydride, iron oxide, rare earth oxide, and hafnium carbide, the powder blending with and suspending in the ceramic precursors at a level in the range 33% to 80% by weight of the composition without sieving the mixture, with the non-oxide ceramic powder to polymeric precursor ratio ranging from 0.5;

1 to 4;

1.

8. The nonaqueous, nonvolatile pre-ceramic paste composition useful for applications requiring high temperature strength and oxidation resistance of claim 7 wherein heat treatment yields ZrB_x ceramic phases with domain sizes less than 0.5 μ

m.