Dispersion for silicon carbide sintered body, green sheet for silicon carbide sintered body and prepreg material for silicon carbide sintered body using the same, and manufacturing method thereof

Patent metadata

Field	Value
Publication number	US-11760697-B2
Application number	US-201917042404-A
Country	US
Kind code	B2
Filing date	Mar 26, 2019
Priority date	Mar 30, 2018
Publication date	Sep 19, 2023
Grant date	Sep 19, 2023

Abstract

Provided are a dispersion for a silicon carbide sintered body having a small environmental load, high dispersibility, and excellent temporal stability, and a manufacturing method thereof.
The dispersion is a dispersion for a silicon carbide sintered body, containing: silicon carbide particles; boron nitride particles; a resin having a hydroxyl group; and water, wherein the dispersion has a pH at 25° C. of less than or equal to 7.0, and the silicon carbide particles and the boron nitride particles have charges of the same sign. The dispersion is manufactured by a manufacturing method of a dispersion for a silicon carbide sintered body, including a mixing step of mixing a water dispersion containing silicon carbide particles, a water dispersion containing boron nitride particles, and an aqueous solution containing a resin having a hydroxyl group.

First claim

The invention claimed is:

1. A dispersion for a silicon carbide sintered body, comprising:
silicon carbide particles;
boron nitride particles;
a resin having a hydroxyl group; and
water,
wherein the dispersion has a pH at 25° C. of less than or equal to 7.0;
wherein the silicon carbide particles are subjected to charge control by aluminum hydroxide coating; and
wherein the silicon carbide particles and the boron nitride particles have charges of the same sign.

2. The dispersion according to claim 1 , wherein the boron nitride particles are subjected to charge control.

3. The dispersion according to claim 1 , wherein the boron nitride particles are subjected to charge control by a cationic polymer.

4. The dispersion according to claim 1 , wherein the resin having a hydroxyl group is selected from the group consisting of polyvinyl alcohol (PVA), polyvinyl butyral (PVB), a glyoxal resin, an acrylic resin, a phenol resin, hydroxyl group-containing polyvinyl pyrrolidone (PVP), hydroxyl group-containing polyester, hydroxyl group-containing silicone, and a hydroxyl group-containing polycarboxylic acid.

5. The dispersion according to claim 3 , wherein the cationic polymer is poly(diallyl dimethyl ammonium chloride), poly(methacryloyloxyethyl trimethyl ammonium chloride), poly(acryl amide-co-diallyl dimethyl ammonium chloride), poly(dimethyl amine-co-epichlorohydrin-co-ethylene diamine), polyethylene imine, ethoxylated polyethylene imine, poly(amidoamine), poly(methacryloyloxyethyl dimethyl ammonium chloride), poly(vinyl pyrrolidone), poly(vinyl imidazole), poly(vinyl pyridine), or poly(vinyl amine).

6. The dispersion according to claim 1 , wherein an average secondary particle size of the coated silicon carbide particles coated with aluminum hydroxide is less than or equal to 2 μm.

7. A green sheet for a silicon carbide sintered body, formed from the dispersion set forth in claim 1 .

8. A prepreg material for a silicon carbide sintered body, formed from the green sheet for a silicon carbide sintered body set forth in claim 7 .

9. A manufacturing method of a dispersion for a silicon carbide sintered body, comprising a mixing step of mixing:
a water dispersion containing silicon carbide particles,
a water dispersion containing boron nitride particles, and
an aqueous solution containing a resin having a hydroxyl group,
wherein the silicon carbide particles and the boron nitride particles have charges of the same sign, and a pH of the dispersion for a silicon carbide sintered body at 25° C. is less than or equal to 7.0,
wherein the method further comprises, before the mixing step:
a preparing step for a water dispersion containing silicon carbide particles of adding a charge control agent and an acid to a raw dispersion containing silicon carbide particles such that pH is in a range of greater than or equal to 9.0 and less than or equal to 12.0, thereby forming coated silicon carbide particles including a coating layer containing a charge control component on a surface of the silicon carbide particles to prepare a water dispersion containing silicon carbide particles; and
in the preparing step for a water dispersion containing silicon carbide particles, the charge control agent is sodium aluminate.

10. The manufacturing method according to claim 9 , further comprising, before the mixing step:
a preparing step for a water dispersion containing boron nitride particles of adding a solution containing a functional polymer to a raw dispersion containing boron nitride particles, thereby forming coated boron nitride particles including a coating layer containing the functional polymer on a surface of the boron nitride particles to prepare a water dispersion containing boron nitride particles.

11. The manufacturing method according to claim 10 , wherein in the preparing step for a water dispersion containing boron nitride particles, the functional polymer is a cationic polymer.

12. The manufacturing method according to claim 11 , wherein the cationic polymer is poly(diallyl dimethyl ammonium chloride), poly(methacryloyloxyethyl trimethyl ammonium chloride), poly(acryl amide-co-diallyl dimethyl ammonium chloride), poly(dimethyl amine-co-epichlorohydrin-co-ethylene diamine), polyethylene imine, ethoxylated polyethylene imine, poly(amidoamine), poly(methacryloyloxyethyl dimethyl ammonium chloride), poly(vinyl pyrrolidone), poly(vinyl imidazole), poly(vinyl pyridine), or poly(vinyl amine).

13. The manufacturing method according to claim 9 , wherein the resin having a hydroxyl group is selected from the group consisting of polyvinyl alcohol (PVA), polyvinyl butyral (PVB), a glyoxal resin, an acrylic resin, a phenol resin, hydroxyl group-containing polyvinyl pyrrolidone (PVP), hydroxyl group-containing polyester, hydroxyl group-containing silicone, and a hydroxyl group-containing polycarboxylic acid.

14. The manufacturing method according to claim 9 , wherein an average secondary particle size of the coated silicon carbide particles is less than or equal to 2 μm.

15. A manufacturing method of a green sheet for a silicon carbide sintered body, comprising a step of obtaining a dispersion for a silicon carbide sintered body by the manufacturing method set forth in claim 9 , and applying the dispersion for a silicon carbide sintered body to a base material.

16. A manufacturing method of a prepreg material for a silicon carbide sintered body, comprising a step of obtaining a green sheet for a silicon carbide sintered body by the manufacturing method set forth in claim 15 , and laminating the green sheet for a silicon carbide sintered body on a fiber base material.

Assignees

• Fujimi Inc

Inventors

• Kamoshida Keigo
• Taguchi Souma
• Ashitaka Keiji
• Miwa Naoya

Classifications

• C04B35/62625 Primary

  Wet mixtures · CPC title

• C04B35/80 Primary

  Fibres, filaments, whiskers, platelets, or the like · CPC title

• C08K3/14

  Carbides · CPC title

• C08L101/06

  containing oxygen atoms {(C08L101/025 takes precedence)} · CPC title

• C01B21/064

  with boron · CPC title