IP Library Granted Patent US 8,657,893
Granted Patent B2
US 8,657,893 · App. 13/022,834 · Granted Feb 25, 2014

Method for producing sintered cubic boron nitride compact

Inventors: Akhmadi Eko Wardoyo (Naka-gun, JP); Itsurou Tajima (Naka-gun, JP); Minoru Akaishi (Kumagaya, JP)
Assignee: Mitsubishi Materials Corporation
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Quick Facts
Patent No.
US 8,657,893
App. No.
13/022,834
Granted
Feb 25, 2014
Kind
B2
Abstract

A method for producing a highly uniform and highly dense sintered cubic boron nitride compact having high hardness by sintering at a milder condition without a binder, is provided. The method includes deflocculating secondary particles in cubic boron nitride starting powders by dispersing the starting powders in a solution of a deflocculant; molding the green compact after removing the solution of the deflocculant from the starting powders; and then sintering the green compact in the presence of a supercritical fluid source in a supercritical state by pressing and heating the green compact together with the supercritical fluid source. The supercritical fluid source can be one or more selected from a group consisted of polyvinylidene chloride, polyvinyl chloride, polyethylene, polypropylene, polystyrene, a polyester and an ABS resin. In the sintering, the pressure is 5 GPa or higher, and the temperature is 1400° C. or higher. According to the method, a highly uniform and highly dense sintered cubic boron nitride sintered compact having high hardness, can be obtained.

Claims (27)

1. A method for producing a sintered cubic boron nitride compact, the method comprising:

a step of deflocculating, in which secondary particles in boron nitride starting powders are deflocculated by dispersing the boron nitride starting powders in a solution of a deflocculant to be a dispersion liquid;

a step of removing, in which the solution of deflocculant is removed from the dispersion liquid after the step of deflocculating;

a step of molding, in which the boron nitride starting powders, which have been deflocculated, are molded to form a green compact after the step of removing; and

a step of sintering, in which the green compact is pressurized at 5 GPa or higher and heated at 1400° C. or higher in the presence of a supercritical fluid source, the supercritical fluid source is put into a supercritical state, and the green compact is sintered, after the step of molding,

wherein a content ratio of the deflocculant in the dispersion liquid ranges from 0.1 to 5 wt % of a sum of the deflocculant and the cubic boron nitride starting powders as a weight.

2. A method for producing a sintered cubic boron nitride compact according to claim 1 ,

wherein the deflocculant is one or more selected from a group consisting of an alkali metal phosphate salt, an alkali metal carbonate salt, an alkali metal silicate salt, an alkali metal aluminate salt, and an alkali metal hydroxide.

3. A method for producing a sintered cubic boron nitride compact according to claim 2 ,

wherein, the deflocculant is one or more selected from a group consisting of sodium phosphate, sodium polyphosphate, sodium metaphosphate, sodium carbonate, sodium silicate, sodium aluminate and sodium hydroxide.

4. A method for producing a sintered cubic boron nitride compact according to claim 3 ,

wherein the deflocculant is sodium metaphosphate.

5. A method for producing a sintered cubic boron nitride compact according to claim 1 ,

wherein the supercritical fluid source is one or more selected from a group consisting of polyvinylidene chloride, polyvinyl chloride, polyethylene, polypropylene, polystyrene, a polyester and an ABS resin.

6. A method for producing a sintered cubic boron nitride compact according to claim 2 ,

wherein the supercritical fluid source is one or more selected from a group consisting of polyvinylidene chloride, polyvinyl chloride, polyethylene, polypropylene, polystyrene, a polyester and an ABS resin.

7. A method for producing a sintered cubic boron nitride compact according to claim 3 ,

wherein the supercritical fluid source is one or more selected from a group consisting of polyvinylidene chloride, polyvinyl chloride, polyethylene, polypropylene, polystyrene, a polyester and an ABS resin.

8. A method for producing a sintered cubic boron nitride compact according to claim 4 ,

wherein the supercritical fluid source is one or more selected from a group consisted of polyvinylidene chloride, polyvinyl chloride, polyethylene, polypropylene, polystyrene, a polyester and an ABS resin.

9. A method for producing a sintered cubic boron nitride compact according to claim 1 , further comprising:

a step of eliminating by vacuuming and heating, in which the deflocculant remaining in the green compact is eliminated by heating the green compact under a vacuum, after the step of molding and before the step of sintering.

10. A method for producing a sintered cubic boron nitride compact according to claim 1 ,

wherein the green compact, a metal foil, and the supercritical fluid source are stacked in a capsule after the step of molding and before the step of sintering, and

the metal foil is made of one or more selected from a group consisting of Zr, Nb, Mo, and Ta.

11. A method for producing a sintered cubic boron nitride compact according to claim 1 ,

wherein a mass ratio of the supercritical fluid source to the cubic boron nitride starting powder ranges from 0.02 to 0.2 wt %.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2011
From: WARDOYO, AKHMADI EKO; TAJIMA, ITSUROU; AKAISHI, MINORU
To: MITSUBISHI MATERIALS CORPORATION
Reel/Frame 025911/0615 →
Priority Claims (1)
JP 2010-026539 · Feb 9, 2010 · national
Continuity (1)
Related Publication 20110192093A1 · Aug 11, 2011