JPH0336780B2 - - Google Patents
Info
- Publication number
- JPH0336780B2 JPH0336780B2 JP60109924A JP10992485A JPH0336780B2 JP H0336780 B2 JPH0336780 B2 JP H0336780B2 JP 60109924 A JP60109924 A JP 60109924A JP 10992485 A JP10992485 A JP 10992485A JP H0336780 B2 JPH0336780 B2 JP H0336780B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- strength
- ceramic material
- powder
- carbonitride
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 8
- 229910021332 silicide Inorganic materials 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910052735 hafnium Inorganic materials 0.000 claims description 4
- 150000002736 metal compounds Chemical class 0.000 claims description 4
- 229910052758 niobium Inorganic materials 0.000 claims description 4
- 229910052715 tantalum Inorganic materials 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- 239000000919 ceramic Substances 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000003779 heat-resistant material Substances 0.000 claims 1
- 229910010293 ceramic material Inorganic materials 0.000 description 13
- 239000010936 titanium Substances 0.000 description 6
- 239000011812 mixed powder Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 150000004767 nitrides Chemical class 0.000 description 4
- 150000001247 metal acetylides Chemical class 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
Landscapes
- Ceramic Products (AREA)
Description
(産業上の利用分野)
本発明は、高温においても室温下と同様の物性
を示す高強度構造材として利用しうる新規な高強
度耐熱セラミツクス材料に関するものである。
(従来の技術)
周期表〜族の遷移金属の炭化物、窒化物、
ホウ化物及びケイ化物は、一般に融点が高く、硬
度その他の機械的特性が優れているため、高強度
構造材として好適なことはよく知られている。な
かでも、炭化物、窒化物は硬度が高く、超硬合金
に代表されるように従来から、その高硬度性を活
かして切削工具材等に利用されてきた。それに対
し、ホウ化物はこれまであまり利用されていな
い。またケイ化物は、わずかに抵抗発熱体として
実用化されている例があるにすぎない。
炭窒化物は焼結性はよいが、粒成長が著しく粗
大組織となるため、その単味焼結体は強度が低
い。またホウ化物は、単味では焼結性が極めて悪
く、焼結させるためには、高温、高圧を必要とす
る。先に本発明者らが提案した炭窒化チタン−ホ
ウ化金属化合物系(特公昭59−18349号)は、炭
窒化物とホウ化物を組み合わせることにより、炭
窒化チタンの粒成長を抑制し、かつホウ化物の焼
結性を改善した高密度かつ、高強度のセラミツク
ス材料である。
しかしながら、このセラミツクス材料は、それ
を製造するのに高温での加熱が必要である上に、
高温化での耐酸化性が不十分である。
他方、ケイ化物については良好な焼結性、耐酸
化性を有することが知られているが、その単味焼
結体は室温において極めて脆いという欠点があ
る。
(発明が解決しようとする課題)
本発明は、従来の炭窒化物−ホウ化物系焼結体
やケイ化物系焼結体がもつ欠点を克服し、高温下
においても室温下におけると同様な優れた機械的
特性を示す、耐熱性高強度構造材として有用な新
規なセラミツクス材料を提供することを目的とし
てなされたものである。
(課題を解決するための手段)
本発明者らは、高強度耐熱セラミツクス材料に
ついて種々研究を重ねた結果、炭窒化物−ホウ化
物系にケイ化物系を複合させた系が、それぞれの
長所を合わせ有すると共に、それぞれの短所を補
つた優れた特性を示すことを見い出し、この知見
に基づいて本発明をなすに至つた。
すなわち、本発明は(A)Ti、Zr、Hf、V、Nb、
Ta、Cr、Mo又はWの炭窒化物及びホウ化物の
中から選ばれた少なくとも1種の金属化合物の粉
末20〜90重量%と、(B)Ti、Zr、Hf、V、Nb、
Ta、Cr又はWのケイ化物の中から選ばれた少な
くとも1種の金属化合物の粉末80〜10重量%の混
合物の焼結体から成る高強度耐熱セラミツクス材
料を提供するものである。
本発明のセラミツクス材料の(A)成分の炭窒化物
は、炭化物、窒化物を個別に用いず原料の段階で
固溶させて用いる。この炭窒化物は、Mを金属と
してM(CαNβ)と表わされるもので、固溶効果
により炭化物、窒化物に比べ機械特性が優れてい
る。原子割合α:βは、10:90〜90:10のものが
好ましい。
また、焼結性をよくし、かつ焼結体組織を微細
化するため、(A)成分及び(B)成分は、平均粒径2μ
m以下の粉末として用いるのが好ましい。
(A)成分と(B)成分の混合割合は、混合粉末全重量
に基づき、(A)成分20〜90重量%、(B)成分80〜10重
量%、好ましくは(A)成分40〜80重量%、(B)成分60
〜20重量%の範囲内で選ばれる。この範囲を逸脱
すると焼結性が悪化するとともに強度が著しく低
下する。特に炭窒化物の場合は、これが多くなる
と焼結体組織が粗大化する傾向にあるので、60重
量%以下にするのが望ましい。他方、ホウ化物の
場合は、これが多すぎると焼結性の低下を生じ空
隙が残るようになる。また、ケイ化物の場合は、
これが多くなりすぎると、硬度が低下し、脆弱に
なる。
(A)成分と(B)成分の混合粉末は、易焼結性であ
り、通常のホツトプレス法や普通焼結法などによ
り容易に焼結し、所望のセラミツクス材料を形成
することができる。
(発明の効果)
本発明のセラミツクス材料は、高融点であり、
また常温においてと同様、高温においても高強
度、高硬度、高靭性という高温構造材として極め
て好適の特性を備えている。また、易焼結性であ
るので製造も容易である。しかも、炭窒化物が少
ない場合は、耐酸化性をも有するという利点もあ
る。このように極めて優れた特性を有する材料で
あり、構造材、耐摩性材料、切削工具材等の他、
耐熱性、高強度、高硬度等が要求される多くの分
野において利用が可能である。
(実施例)
次に、実施例により本発明をさらに詳細に説明
する。
実施例 1
Ti(C50N50)粉末を40重量部、TiB2粉末を20重
量部及びNbSi2粉末を40重量部の割合で秤量し、
均一に混合して混合粉末組成物を調整した。次い
でこの混合粉末組成物を黒鉛型に充填し、真空
中、20MPaの一軸加圧のもと、1600℃において、
30分間加圧焼成し、セラミツクス材料を製造し
た。得られたセラミツクス材料の抗折力
1100MN/m2、硬度は1680Kg/mm2、破壊靭性値は
4.7MN/m3/2であり、空〓はなかつた。
実施例2〜19、比較例1〜10
原料の混合粉末組成物の組成を変え、次表に示
す焼結条件を用いて、セラミツクス材料を製造し
た。このようにして得たセラミツクス材料の特性
を次表に示す。なお、表中TiCNはTi(C50N50)
の略である。
(Field of Industrial Application) The present invention relates to a novel high-strength heat-resistant ceramic material that can be used as a high-strength structural material that exhibits physical properties similar to those at room temperature even at high temperatures. (Prior art) Carbides, nitrides, etc. of transition metals from groups of the periodic table.
It is well known that borides and silicides are suitable as high-strength structural materials because they generally have high melting points and excellent hardness and other mechanical properties. Among these, carbides and nitrides have high hardness, and have traditionally been used in cutting tool materials and the like by taking advantage of their high hardness, as typified by cemented carbide. In contrast, borides have not been widely used so far. Furthermore, there are only a few examples of silicides being put to practical use as resistance heating elements. Although carbonitrides have good sinterability, their grains grow significantly and form a coarse structure, so their simple sintered bodies have low strength. In addition, borides have extremely poor sinterability when used alone, and require high temperature and pressure to sinter. The titanium carbonitride-metal boride compound system (Japanese Patent Publication No. 59-18349) proposed by the present inventors suppresses the grain growth of titanium carbonitride by combining carbonitride and boride, and It is a high-density and high-strength ceramic material with improved sinterability of boride. However, this ceramic material requires heating at high temperatures to manufacture it, and
Oxidation resistance at high temperatures is insufficient. On the other hand, although silicides are known to have good sinterability and oxidation resistance, they have the disadvantage that their simple sintered bodies are extremely brittle at room temperature. (Problems to be Solved by the Invention) The present invention overcomes the drawbacks of conventional carbonitride-boride-based sintered bodies and silicide-based sintered bodies, and has the same superiority at high temperatures as at room temperature. The purpose of this work was to provide a new ceramic material useful as a heat-resistant, high-strength structural material that exhibits excellent mechanical properties. (Means for Solving the Problems) As a result of various studies on high-strength heat-resistant ceramic materials, the present inventors found that a system that combines a carbonitride-boride system with a silicide system has the advantages of each. The present inventors have discovered that they exhibit excellent characteristics that compensate for the shortcomings of each, and have accomplished the present invention based on this knowledge. That is, the present invention provides (A) Ti, Zr, Hf, V, Nb,
20 to 90% by weight of powder of at least one metal compound selected from carbonitrides and borides of Ta, Cr, Mo or W; (B) Ti, Zr, Hf, V, Nb,
The present invention provides a high-strength, heat-resistant ceramic material comprising a sintered body of a mixture of 80 to 10% by weight of powder of at least one metal compound selected from silicides of Ta, Cr, or W. In the carbonitride component (A) of the ceramic material of the present invention, carbide and nitride are not used individually, but are used as a solid solution in the raw material stage. This carbonitride is expressed as M(CαNβ), where M is a metal, and has superior mechanical properties compared to carbides and nitrides due to the solid solution effect. The atomic ratio α:β is preferably 10:90 to 90:10. In addition, in order to improve sinterability and refine the structure of the sintered body, components (A) and (B) have an average particle size of 2 μm.
It is preferable to use it as a powder with a particle size of m or less. The mixing ratio of component (A) and component (B) is 20 to 90% by weight of component (A) and 80 to 10% by weight of component (B), preferably 40 to 80% of component (A), based on the total weight of the mixed powder. Weight%, component (B) 60
Selected within the range of ~20% by weight. Outside this range, the sinterability deteriorates and the strength significantly decreases. Particularly in the case of carbonitrides, if the carbonitride content increases, the structure of the sintered body tends to become coarse, so it is desirable to keep the content to 60% by weight or less. On the other hand, in the case of boride, if the content is too large, the sinterability deteriorates and voids remain. Also, in the case of silicides,
If this amount increases too much, the hardness decreases and the material becomes brittle. The mixed powder of components (A) and (B) is easily sinterable, and can be easily sintered by a normal hot pressing method or ordinary sintering method to form a desired ceramic material. (Effect of the invention) The ceramic material of the invention has a high melting point,
Furthermore, it has properties that are extremely suitable as a high-temperature structural material, such as high strength, high hardness, and high toughness at high temperatures as well as at room temperature. Moreover, since it is easy to sinter, it is easy to manufacture. Moreover, when the carbonitride content is small, it also has the advantage of having oxidation resistance. In this way, it is a material with extremely excellent properties, and is used as a structural material, wear-resistant material, cutting tool material, etc.
It can be used in many fields that require heat resistance, high strength, high hardness, etc. (Example) Next, the present invention will be explained in more detail with reference to Examples. Example 1 40 parts by weight of Ti(C 50 N 50 ) powder, 20 parts by weight of TiB 2 powder, and 40 parts by weight of NbSi 2 powder were weighed,
A mixed powder composition was prepared by uniformly mixing. Next, this mixed powder composition was filled into a graphite mold, and heated at 1600°C under uniaxial pressure of 20 MPa in a vacuum.
Pressure firing was performed for 30 minutes to produce a ceramic material. Transverse rupture strength of the obtained ceramic material
1100MN/m 2 , hardness 1680Kg/mm 2 , fracture toughness value
It was 4.7MN/m 3/2 , and there was no empty space. Examples 2 to 19, Comparative Examples 1 to 10 Ceramic materials were manufactured by changing the composition of the raw material mixed powder composition and using the sintering conditions shown in the following table. The properties of the ceramic material thus obtained are shown in the table below. In addition, TiCN in the table is Ti(C 50 N 50 )
It is an abbreviation of
【表】【table】
【表】
なお、上記の表中の実施例15で得たセラミツク
スについて、1000℃における酸化試験を行つたと
ころ、表面にガラス相が形成され、酸化は進行し
なかつた。[Table] Note that when an oxidation test was conducted at 1000°C on the ceramics obtained in Example 15 in the above table, a glass phase was formed on the surface and oxidation did not proceed.
Claims (1)
Wの炭窒化物及びホウ化物の中から選ばれた少な
くとも1種の金属化合物の粉末20〜90重量%と、
(B)Ti、Zr、Hf、V、Nb、Ta、Cr又はWのケイ
化物の中から選ばれた少なくとも1種の金属化合
物の粉末80〜10重量%の混合物の焼成体から成る
高強度耐熱セラミツクス材料。1 (A) 20 to 90% by weight of powder of at least one metal compound selected from carbonitrides and borides of Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, or W;
(B) High-strength, heat-resistant material made of a sintered body of a mixture of 80 to 10% by weight of powder of at least one metal compound selected from silicides of Ti, Zr, Hf, V, Nb, Ta, Cr, or W. Ceramics materials.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60109924A JPS61266361A (en) | 1985-05-21 | 1985-05-21 | High strength heat insulating ceramic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60109924A JPS61266361A (en) | 1985-05-21 | 1985-05-21 | High strength heat insulating ceramic material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61266361A JPS61266361A (en) | 1986-11-26 |
| JPH0336780B2 true JPH0336780B2 (en) | 1991-06-03 |
Family
ID=14522568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60109924A Granted JPS61266361A (en) | 1985-05-21 | 1985-05-21 | High strength heat insulating ceramic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61266361A (en) |
-
1985
- 1985-05-21 JP JP60109924A patent/JPS61266361A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61266361A (en) | 1986-11-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |