CN102557664A - Pressureless sintering production process of thulium oxide-samarium oxide ceramic - Google Patents
Pressureless sintering production process of thulium oxide-samarium oxide ceramic Download PDFInfo
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- CN102557664A CN102557664A CN2010106208912A CN201010620891A CN102557664A CN 102557664 A CN102557664 A CN 102557664A CN 2010106208912 A CN2010106208912 A CN 2010106208912A CN 201010620891 A CN201010620891 A CN 201010620891A CN 102557664 A CN102557664 A CN 102557664A
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- trioxide
- samarium
- silicon nitride
- pressureless sintering
- production technique
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Abstract
The invention relates to the technical field of ceramic material, particularly to a pressureless sintering production process of high-performance silicon nitride (Si3N4) ceramic by using thulium oxide and samarium oxide as additives. The silicon nitride ceramic comprises the following components in percentage by mass: 3-7% of thulium oxide, 5-8% of samarium oxide, and 85-92% of silicon nitride. For overcoming the shortages in the prior art, the invention provides a pressureless sintering production process of high-performance silicon nitride ceramic by using thulium oxide and samarium oxide as additives, and the method can be widely used for preparing components and parts in the fields of chemical industry, machinery, metallurgy, aerospace, etc.
Description
[technical field]
The present invention relates to a kind of technical field of ceramic material, specifically is the method for a kind of trioxide Samarium trioxide as additive pressureless sintering production high-performance silicon nitride ceramics.
[background technology]
Silicon nitride ceramics has excellent mechanical behavior under high temperature, is acknowledged as one of the most rising high temperature resistant structure ceramics.Silicon nitride is as a kind of covalent linkage platform thing, and spread coefficient is little, does not have fusing point, decomposes ammonification and silicon about 2173K, is difficult to sintering.Common silicon nitride ceramics respond sintering and hot pressed sintering, the reaction sintering density is poor, poor mechanical property, though hot pressed sintering density is high, mechanical property is good, cost is higher, is difficult to scale operation.And pressureless sintering falls between, because silicon nitride ceramics is the covalent linkage compound, and the pressureless sintering difficulty, the density that improves the pressureless sintering silicon nitride ceramics becomes the research focus, adds rare earth oxide usually as sintering aid, like iridium oxide.But the cost of iridium oxide is higher, and is unfavorable for the application of silicon nitride.We select for use the trioxide Samarium trioxide as sintered density and the mechanical property of additive to improve silicon nitride for this reason.
[summary of the invention]
The objective of the invention is to overcome the deficiency of prior art, the method for a kind of trioxide Samarium trioxide as additive pressureless sintering production high-performance silicon nitride ceramics is provided.Working method of the present invention is simple, and cost is low, is prone to realize industrialization production; The silicon nitride ceramics that trioxide Samarium trioxide of the present invention is produced as additive pressureless sintering has the density height, the characteristics that mechanical property is good.
The present invention realizes through following technical scheme:
The silicon nitride ceramics that trioxide Samarium trioxide involved in the present invention is produced as additive pressureless sintering, component and mass percentage content are: trioxide 3%～7%, Samarium trioxide 5%～8%, silicon nitride 85%～92%.
3～6 microns of described trioxide granularities, 5～7 microns of Samarium trioxide granularities, 0.4～0.7 micron of silicon nitride granularity.
The silicon nitride ceramics method that trioxide Samarium trioxide involved in the present invention is produced as additive pressureless sintering comprises the steps:
Step 1; Take by weighing trioxide Samarium trioxide and silicon nitride ceramics powder respectively; In planetary ball mill, change mixing 2 hours with PM 270～330, dispersion medium is an absolute ethyl alcohol, subsequently 60 ℃ of oven dry; Time is 2～3 hours, trioxide Samarium trioxide that obtains mixing and silicon nitride ceramics mixed powder;
Step 2 at 75～100Mpa forming under the pressure, forms biscuit with the mixed powder of step 1;
Step 3, with the biscuit in the step 2 in vacuum carbon tube furnace under nitrogen protection, under 1400～1550 ℃ of temperature, be incubated 12～18 hours.
Step 4 is taken out the silicon nitride ceramics that burns till in the step 3 detection volume density and mechanical property.
In the step 1, the weight percent of said trioxide is 3%～7%, and the weight percent of Samarium trioxide is 5%～8%, and the weight percent of silicon nitride is 85%～92%.
In the step 1, α-Si in the said silicon nitride
3N
4Content is greater than 90%.
In the step 1, said trioxide Samarium trioxide content is all greater than 98%.
In the step 3, said nitrogen gas pressure is 1～2 normal atmosphere.
In the step 4, said mechanical property is a folding strength.
Among the present invention, described trioxide Samarium trioxide plays the effect of sintering aid, under 1400～1550 ℃ of high temperature sintering conditions, forms liquid phase, makes the silicon nitride ceramics densification.
The present invention has following beneficial effect: the silicon nitride ceramics compactness extent is high, and mechanical property is good, satisfies the actual needs that use.This preparation method is simple, and cost is low, is prone to realize industrialization production.
[embodiment]
Below in conjunction with embodiment the present invention is described further.Production technology of the present invention is to implement easily to this professional people.Present embodiment provided detailed embodiment and process, but protection scope of the present invention is not limited to following embodiment being to implement under the prerequisite with technical scheme of the present invention.The experimental technique of unreceipted actual conditions in the following example, usually according to normal condition, or the condition of advising according to manufacturer.
Embodiment
The trioxide Samarium trioxide is Ganzhou Jiarun novel material ltd, and silicon nitride powder is the M11 powder that German Starck company produces.Take by weighing 3% trioxide, 5% Samarium trioxide and 92% silicon nitride powder respectively according to weight percent.
Above-mentioned two kinds of powder (QM-3SP2 of Nanjing Univ. Instrument Factory type) in planetary ball mill are mixed, and rotating speed 300 changes 1.5 hours time.With the forming under the pressure of powder mix, biscuit (the flourish electric furnace ZT-40-20 of ltd of Shanghai occasion type) 1450 ℃ in vacuum carbon tube furnace is incubated 16 hours at 80Mpa.
The volume density of the silicon nitride ceramics that present embodiment obtains is 3.41g/cm
3, folding strength is 623Mpa.
Claims (7)
1. the silicon nitride ceramics produced as additive pressureless sintering of the related trioxide Samarium trioxide of the production technique of trioxide Samarium trioxide pottery pressureless sintering; Component and mass percentage content are: trioxide 3%～7%; Samarium trioxide 5%～8%, silicon nitride 85%～92%.3～6 microns of described trioxide granularities, 5～7 microns of Samarium trioxide granularities, 0.4～0.7 micron of silicon nitride granularity.
2. the silicon nitride ceramics method that the related trioxide Samarium trioxide of production technique of a kind of trioxide Samarium trioxide pottery according to claim 1 pressureless sintering is produced as additive pressureless sintering comprises the steps:
Step 1; Take by weighing trioxide Samarium trioxide and silicon nitride ceramics powder respectively; In planetary ball mill, change mixing 2 hours with PM 270～330, dispersion medium is an absolute ethyl alcohol, subsequently 60 ℃ of oven dry; Time is 2～3 hours, trioxide Samarium trioxide that obtains mixing and silicon nitride ceramics mixed powder;
Step 2 at 75～100Mpa forming under the pressure, forms biscuit with the mixed powder of step 1;
Step 3, with the biscuit in the step 2 in vacuum carbon tube furnace under nitrogen protection, under 1400～1550 ℃ of temperature, be incubated 12～18 hours.
Step 4 is taken out the silicon nitride ceramics that burns till in the step 3 detection volume density and mechanical property.
3. the production technique of a kind of trioxide Samarium trioxide pottery according to claim 2 pressureless sintering; The weight percent that it is characterized in that trioxide described in the step 1 is 3%～7%; The weight percent of Samarium trioxide is 5%～8%, and the weight percent of silicon nitride is 85%～92%.
4. the production technique of a kind of trioxide Samarium trioxide pottery according to claim 2 pressureless sintering is characterized in that in the step 1 α-Si in the said silicon nitride
3N
4Content is greater than 90%.
5. the production technique of a kind of trioxide Samarium trioxide pottery according to claim 2 pressureless sintering is characterized in that in the step 1 that content is all greater than 98% in the said trioxide Samarium trioxide.
6. the production technique of a kind of trioxide Samarium trioxide pottery according to claim 2 pressureless sintering is characterized in that in the step 3 that said nitrogen gas pressure is 1～2 normal atmosphere.
7. the production technique of a kind of trioxide Samarium trioxide pottery according to claim 2 pressureless sintering is characterized in that in the step 4 that said mechanical property is a folding strength.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010106208912A CN102557664A (en) | 2010-12-29 | 2010-12-29 | Pressureless sintering production process of thulium oxide-samarium oxide ceramic |
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| CN2010106208912A CN102557664A (en) | 2010-12-29 | 2010-12-29 | Pressureless sintering production process of thulium oxide-samarium oxide ceramic |
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| CN102557664A true CN102557664A (en) | 2012-07-11 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116283291A (en) * | 2023-03-20 | 2023-06-23 | 中国矿业大学(北京) | Insulation tube preparation method |
-
2010
- 2010-12-29 CN CN2010106208912A patent/CN102557664A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116283291A (en) * | 2023-03-20 | 2023-06-23 | 中国矿业大学(北京) | Insulation tube preparation method |
| CN116283291B (en) * | 2023-03-20 | 2024-02-23 | 中国矿业大学(北京) | Insulation tube preparation method |
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Application publication date: 20120711 |