Silicon nitride ceramic material for mobile phone rear cover and preparation method therefor

1. A preparation method of silicon nitride ceramic for a mobile phone rear cover, comprising:

(1) dispersing a mixture containing a silicon source, an oxide of a transition metal, a first sintering aid and an oxide of rare earth metal in an organic solvent to obtain a mixture of raw materials;

(2) adding a dispersant to the mixture of raw materials and then adding a binder and/or a plasticizer and mixing evenly to obtain a mixture to be shaped; and

(3) shaping the mixture to be shaped into a green body, and sintering the green body to obtain the silicon nitride ceramic,

wherein the oxide of the transition metal is chromic oxide or hafnium oxide and serves as a first colorant,

wherein the first sintering aid is selected from the group consisting of Al 2 O 3 , AlN, CaO, MgO, and SiO 2 ,

wherein the oxide of the rare earth metal is selected from the group consisting of yttrium oxide, europium oxide, and erbium oxide and serves both as a second sintering aid and a second colorant,

wherein a mass ratio of the first sintering aid and the second sintering aid is 3:(5 to 8),

wherein the silicon source is a silicon nitride powder and/or a silicon powder, and the mass ratio of the silicon source, the first colorant, and the mixture of the first and the second sintering aid is 160:2:15, and the mass of the silicon source is converted into that of silicon nitride for calculation, and

wherein the silicon nitride ceramic has the following characteristics:

a density of 3.2 to 3.4 g/cm 3 ;

a toughness of more than 12 MPa·m 1/2 ;

a strength of 500 MPa to 1,100 MPa;

a thermal conductivity of 40 W/m·K to 70 w/m·K;

a dielectric constant of 7.4 to 9.4;

a dielectric loss of 10×10 −4 to 15×10 −4 ; and

a relative density of 95.0% to 99.5%.

2. The preparation method of claim 1 , wherein

the particle size of the silicon nitride powder ranges from 0.5 μm to 20 μm, and/or the particle size of the silicon powder ranges from 0.2 μm to 30 μm.

3. The preparation method of claim 1 , wherein

the organic solvent is selected from the group consisting of ethanol, butanone, toluene, n-hexane, methanol, xylene, n-propanol, and n-butanol,

an addition amount of the organic solvent is 14% to 50% of the total mass of the silicon source, the first colorant, and the sintering aid,

the dispersant is selected from the group consisting of glycerol trioleate, phosphate, castor oil, herring oil, ascorbic acid, and terpineol, and

an addition amount of the dispersant is 0.5% to 4% of the total mass of the silicon source, the first colorant, and the sintering aid.

4. The preparation method of claim 1 , wherein

the binder is polyvinyl butyral and/or polymethylmethacrylate, and an addition amount of the binder is 0.5% to 10% of the silicon source, the first colorant, and the sintering aid; and/or

the plasticizer is dibutyl phthalate and/or butyl benzyl phthalate, and an addition amount of the plasticizer is 0.5 to 10% of the total mass of the silicon source, the first colorant, and the sintering aid.

5. The preparation method of claim 3 , wherein the organic solvent is a binary mixed solvent of ethanol/butanone, ethanol/toluene, ethanol/n-hexane, butanone/methanol, xylene/n-propanol, or xylene/n-butanol, with a mass ratio of 1:(0.2 to 8).

6. The preparation method of claim 1 , wherein

the shaping is injection molding, dry pressing, or tape casting,

the sintering is pressureless sintering, gas pressure sintering, or high temperature isostatic pressing sintering, the sintering temperature is 1,600° C. to 1,950° C., the sintering time is 1 hour to 12 hours, the sintering pressure is 0.1 MPa to 10 MPa, and the heating rate is 1° C./min to 10° C./min during a heating stage of the sintering, and/or

the mixing in step (2) and/or step (3) is performed by ball milling.

7. The preparation method of claim 1 , wherein

the silicon source is the silicon powder, and

the preparation method further comprises a step of nitriding the silicon powder, the nitriding temperature being 1,300° C. to 1,500° C., the nitriding time being 6 hours to 10 hours, and a nitrogen source for nitridation being nitrogen or a mixture of nitrogen and hydrogen with a volume ratio of (90 to 95):(10 to 5).

8. The preparation method of claim 1 , wherein

the preparation method further comprises a step of defoaming the material to be shaped before forming; and/or

the green body is formed into a mobile phone rear cover in step (3).