Highly shock-resistant ceramic material
Ceramic material of high impact strength, in particular based on Si 3 N 4 or ZrO 2 , having an HV10 hardness of not more than 15.5 GPa and an E modulus at room temperature of less than 330 GPa, wherein the material contains 0.2 to 5 wt. % of carbon particles which have a maximum particle size of 5 μm, a process for the preparation of the ceramic material and the use thereof, in particular as roller bodies in bearings.
1 . A ceramic material comprising,
0.2 to 5 wt. % of carbon particles having a maximum particle size of 5 μm, wherein said ceramic material has,
an HV10 hardness of not more than 15.5 GPa, and
an E modulus at room temperature of less than 330 GPa.
2 . The ceramic material of claim 1 wherein said ceramic material comprises 0.2 to 3 wt. % of carbon particles.
3 . The ceramic material of claim 1 wherein said ceramic material has a density corresponding to at least 98.5% of theoretical density.
4 . The ceramic material of claim 1 where said ceramic material has:
an RT flexural strength of at least 750 MPa,
a fracture toughness of at least 5.5 Mpa m 1/2 , and
a Poisson ratio or transverse contraction coefficient at 25° C. of ≦0.3.
5 . The ceramic material of claim 1 wherein said ceramic material is free of at least one of macroscopic defects larger than 20 μm and optical heterogeneities larger than 50 μm.
6 . The ceramic material of claim 1 wherein said ceramic material is selected from the group consisting of silicon nitride ceramic material and zirconium dioxide ceramic material.
7 . The ceramic material of claim 6 wherein said ceramic material is silicon nitride ceramic material and the ceramic material further comprises particles of at least one of carbide, nitride, carbonitride, boride and silicide compounds
of elements of groups IVB, VB and VIB of the periodic table, or
of silicon, or
of iron,
further wherein said particles have a maximum size that does not exceed 10 μm, and the maximum concentration of said particles is <50 vol. %.
8 . A process of preparing a ceramic material comprising
0.2 to 5 wt. % of carbon particles having a maximum particle size of 5 μm,
wherein said ceramic material has, an HV10 hardness of not more than 15.5 GPa, and an E modulus at room temperature of less than 330 GPa, said process comprising the steps of:
providing raw materials;
subjecting the raw materials to wet grinding thereby forming wet around raw materials;
adding one or more organic additives to said wet ground raw materials, thereby forming intermediate wet around materials;
drying and granulating the intermediate wet around materials; and
shaping the dried and granulated intermediate wet around materials by means of heating and heating of the organic additives,
wherein process conditions are selected such that carbon particles are separated out, and said ceramic material is free of at least one of macroscopic defects larger than 20 μm and optical heterogeneities larger than 50 μm.
9 . The process of claim 8 further comprising sieving a suspension, formed during wet grinding, over a magnetic separator and a fine filter having a maximum filter pore size of 50 μm.
10 . The process of claim 9 wherein said raw materials comprise Si 3 N 4 powder, sintering auxiliaries and optionally a dispersing auxiliary, and said organic additives are selected from at least one member of the group consisting of polyacrylates, polyvinyl alcohols, polyglycols and polyvinylpyrrolidone,
said process further comprising,
forming said raw materials into a slip,
wet grinding the slip,
adding said organic additives to the slip, thereby forming a mixture
drying the mixture at temperatures below 200° C.,
granulating the dried mixture,
shaping the granulated and dried mixture by heating thoroughly at temperatures of between 100 and 400° C. for a duration of 0.5 to 4 h in air, or between 100 and 800° C. for a duration of 0.5 to 4 h in an inert atmosphere or in vacuo, thereby forming a shaped body, and
sintering the shaped body by means of a two-stage process comprising a first stage and a second stage wherein
in the first stage the shaped body is treated for 0.5 to 5 h at a temperature of up to 2,000° C. under an N 2 or inert gas pressure of 1 to 50 bar, and
in the second stage the shaped body is treated for 0.5 to 2.5 h at a temperature of up to 2,000° C. under an N 2 or inert gas pressure of 50 to 2,500 bar.
11 . The process of claim 9 wherein said raw materials comprise ZrO 2 powder, sintering auxiliaries, and optionally a dispersing auxiliary, and said organic additives comprise at least one member of the group consisting of polyacrylates, polyvinyl alcohols, polyglycols and/or polyvinylpyrrolidone,
said process further comprising,
processing said raw materials into a slip,
wet grinding the slip, adding said organic additives to the slip, thereby forming a mixture,
drying the mixture at temperatures below 250° C.,
granulating the dried mixture,
shaping the dried and granulated mixture by heating thoroughly at temperatures of between 100 and 400° C. for a duration of 0.5 to 4 h in air, or between 100 and 800° C. for a duration of 0.5 to 4 h in an inert atmosphere or in vacuo, thereby forming a shaped body, and
sintering the shaped body in a two-stage process comprising a first stage and a second stage, wherein
in the first stage the shaped body is treated for 0.5 to 5 h at a temperature of up to 1,700° C. under an N 2 or inert gas pressure of 1 to 50 bar, and
in the second stage it the shaped body is treated for 0.5 to 2.5 h at a temperature of up to 1,700° C. under an N 2 or inert gas pressure of 50 to 2,500 bar.
12 . An article of manufacture comprising the ceramic material of claim 1 wherein said article of manufacture is selected from the group consisting of bearing roller bodies, engine valves and tool inserts.