JPS5891145A - Titanium oxide-base colored sintered alloy - Google Patents
Titanium oxide-base colored sintered alloyInfo
- Publication number
- JPS5891145A JPS5891145A JP18822081A JP18822081A JPS5891145A JP S5891145 A JPS5891145 A JP S5891145A JP 18822081 A JP18822081 A JP 18822081A JP 18822081 A JP18822081 A JP 18822081A JP S5891145 A JPS5891145 A JP S5891145A
- Authority
- JP
- Japan
- Prior art keywords
- phase
- sintered alloy
- titanium oxide
- colored sintered
- based colored
- 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.)
- Granted
Links
- 229910045601 alloy Inorganic materials 0.000 title claims abstract description 24
- 239000000956 alloy Substances 0.000 title claims abstract description 24
- 229910052719 titanium Inorganic materials 0.000 title claims abstract description 7
- 239000010936 titanium Substances 0.000 title claims description 8
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title claims description 4
- 238000005245 sintering Methods 0.000 claims abstract description 6
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 6
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 5
- 239000012535 impurity Substances 0.000 claims abstract description 5
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 5
- 229910052796 boron Inorganic materials 0.000 claims abstract description 4
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 4
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 4
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 4
- 229910052715 tantalum Inorganic materials 0.000 claims abstract description 3
- 229910052802 copper Inorganic materials 0.000 claims abstract 3
- 239000011230 binding agent Substances 0.000 claims description 17
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 11
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 239000010953 base metal Substances 0.000 claims description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052737 gold Inorganic materials 0.000 claims description 3
- 239000010931 gold Substances 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 206010011224 Cough Diseases 0.000 claims 1
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical group [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 claims 1
- 238000005260 corrosion Methods 0.000 abstract description 7
- 230000007797 corrosion Effects 0.000 abstract description 7
- 229910052751 metal Inorganic materials 0.000 abstract description 7
- 239000002184 metal Substances 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 6
- 229910052742 iron Inorganic materials 0.000 abstract description 3
- 150000002739 metals Chemical group 0.000 abstract description 3
- 229910052750 molybdenum Inorganic materials 0.000 abstract description 3
- 229910052758 niobium Inorganic materials 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 239000012071 phase Substances 0.000 description 31
- 239000000463 material Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000005728 strengthening Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 241000951471 Citrus junos Species 0.000 description 1
- 229910001347 Stellite Inorganic materials 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- AHICWQREWHDHHF-UHFFFAOYSA-N chromium;cobalt;iron;manganese;methane;molybdenum;nickel;silicon;tungsten Chemical compound C.[Si].[Cr].[Mn].[Fe].[Co].[Ni].[Mo].[W] AHICWQREWHDHHF-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
本発明は、腕峙計ケース、ネクタイピン、ブローチ等の
装飾品用部材に適し7’jal化チタン基有色焼結合金
に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a 7'jalized titanium-based colored sintered alloy suitable for ornamental parts such as watch cases, tie clips, and brooches.
従来、装飾品用部材には、ステンレス−、ステライト、
黄銅、アルミ合金等の表面を鏡面光沢の状態にして用い
られていたがこれらはいずれもビッカース硬度で200
以下と表面硬度が低く他の無機物又は硬質金属等で容易
に傷が付き装飾的価値が低下すると云う欠点があつ友。Conventionally, materials for decorative items include stainless steel, stellite,
Brass, aluminum alloy, and other materials were used with mirror-glossy surfaces, all of which have a Vickers hardness of 200.
It has the disadvantage that its surface hardness is low and it is easily scratched by other inorganic substances or hard metals, reducing its decorative value.
この欠点を補うものとして、近年WC,TaO又はTi
e 基硬質合金あるいはTiN被覆又は’ric被蝋t
−施した47N横合金を装飾品用部材に用いられるよう
になってきた。これら硬質合金又は植機合金を用いたも
のは、耐食性及び耐スクラッチ性の改良と云う点に於て
は充分に目的を達成したが尚、次のような欠点を克服す
るまでには到っていない。In order to compensate for this drawback, in recent years WC, TaO or Ti
e Base hard alloy or TiN coating or 'ric brazing t
-The processed 47N horizontal alloy has come to be used for decorative parts. Although these hard alloys or implant alloys have fully achieved their objectives in terms of improving corrosion resistance and scratch resistance, they have not yet overcome the following drawbacks. do not have.
即ち、WC及びTaO基硬質台金は、高価である上に比
重が大きく携帯用装飾品としては不向きでめりwe及び
TiC基硬質合金並びK TiC被榎被合合金黒灰色の
単調な色彩で装飾効果に対する要求を完全に満していな
い。又、被覆台金では、台表面に色調むらが生じ装飾品
としての価値がなくなると云う欠点が有る。That is, WC and TaO-based hard base metals are expensive and have a large specific gravity, making them unsuitable for use as portable accessories. Does not fully meet the requirements for decorative effects. In addition, coated base metals have the disadvantage that color tone unevenness occurs on the base surface, rendering them useless as decorative items.
本発明の焼結合金は、上述したような欠点を解決したも
のて、軽量で安価な酸化チタンの中で4低級酸化物であ
るTiOに着目し、丁10の美麗な黄金色と高硬度性を
生かすと共に緻密で装飾品用部材としての合金特性を完
成したものである。The sintered alloy of the present invention solves the above-mentioned drawbacks, and focuses on TiO, which is a lower oxide of titanium oxide, which is lightweight and inexpensive, and has a beautiful golden color and high hardness. It is a material that takes full advantage of the properties of the alloy and has perfected the properties of the alloy as a dense material for decorative items.
即ち、本発明の焼結合金は、美麗な黄金色と高硬度な特
性【有する丁10から成る硬質相とこのTiOとの濡れ
性、強度、焼結性及び緻密性の向上に優れたFe、N1
、COの中から選dれficll[以上の結合相2〜6
0重tsと不可避不純物とから成る焼結合金でおる。又
、必要ならは、上記結合相の1部に焼結性、耐食性及び
結合相の1溶強化を目的にしてTi、Zr、 If、
V、 Nb、 Ta、 W。That is, the sintered alloy of the present invention has a beautiful golden color and high hardness properties. N1
, CO [bonded phase 2 to 6]
It is made of a sintered alloy consisting of zero weight ts and inevitable impurities. If necessary, Ti, Zr, If,
V, Nb, Ta, W.
Or%Mo、 At、 81、Mn%Ou、B の中か
ら選ばれた1z以上から成る金lI4ヲ結合相に対して
0.5〜40重1ll−置換しても良く、史に必要なら
は上記結合相の1%に耐食性及び結合相O分散強化を目
的にしてAt203、Y2O3,ZrO2、MPOの中
から選ばれた1種以上から成る酸化物を結合相に対して
0.5〜25重量−置換して鴨よい。これら結合相の1
部に置換するT1、Zr、 Hf、 V。Or%Mo, At, 81, Mn%Ou, B may be substituted 0.5 to 40 times with respect to the gold lI4 bonded phase consisting of 1z or more selected from 81, Mn%Ou, B, if necessary for the history. To 1% of the binder phase, an oxide consisting of one or more selected from At203, Y2O3, ZrO2, and MPO is added to 1% of the binder phase by weight of 0.5 to 25% for the purpose of strengthening corrosion resistance and O dispersion in the binder phase. - It's good to replace it. One of these bonded phases
T1, Zr, Hf, V.
M b、 Ta、 W、 Or、 Mo、ムj、 81
、Mn%Ou。Mb, Ta, W, Or, Mo, Muj, 81
, Mn%Ou.
Bの中から選はれた1種以上から成る金属とムt203
、Y2O1、Zr0z、MfOの中から選ばれた1種以
上から成る酸化@は同時に置換しても焼結性、耐食性及
び結合相強化に対する効果がある。Metal made of one or more types selected from B and Mut203
, Y2O1, Zr0z, and MfO, even when substituted at the same time, it has effects on sinterability, corrosion resistance, and strengthening of the binder phase.
上記T10から成る硬質相の換りにTiO1〜99に蓋
−とこのTiOの黄金色ヲ振わずに結合相との薗れ性、
焼結性及びwL缶性に役立つ’riN、 ZrN。Instead of the hard phase consisting of T10, TiO1 to 99 is used as a cover, and the golden color of this TiO is not shaken and the bonding phase is melted.
'riN, ZrN useful for sintering properties and wL can properties.
HfN、 Tag、 Tag、 1Jbcの中から選ば
れた1種以上99〜1重iisとから成る硬質相が40
〜98重量−とFe、Ni、CaO中から選はれた1種
以上の結合相が2〜604:Atチと不可避不純物とか
ら成る焼結合金にすると黄金色の色調のコントロールが
一層容易になる。又硬質相中にTiM、 ZrM。A hard phase consisting of one or more selected from HfN, Tag, Tag, 1 Jbc and 99 to 1 IIS is 40
If the sintered alloy is made of ~98% by weight and one or more binder phases selected from Fe, Ni, and CaO consisting of 2~604:At and unavoidable impurities, the golden color tone can be more easily controlled. Become. Also, TiM and ZrM are included in the hard phase.
HfN、 Tag、 Tag、 NbOの中から選はれ
た1種以上のものが含有していると必要ならば結合相の
1部Mft”、zrSHfs V% NbX”% Ws
C1Mo%*z、 +31、Mn、 C!u、 Bの
中から選ばれた1柚以上および/またはhtzos、l
og、 ZrCHl[0の中から選ばれた1株以上によ
って置換すると効果がよ抄強く出てくるので望ましい。If necessary, a part of the bonded phase may contain one or more selected from HfN, Tag, Tag, NbO.
C1Mo%*z, +31, Mn, C! One or more yuzu selected from u, B and/or htzos, l
It is preferable to replace it with one or more strains selected from ZrCHl[0, as the effect will be stronger.
本発明の焼結合金に含有する硬質相の主成分であるTi
Oは、T1元素と0元素の比率が1:lでなくても良く
、低級順化チタンとして安定な範囲内で0元素が増減し
て微妙な色調の変化があってもO元素鍾のコントロール
及び結合相蓋及び種類のコントロールによって一定の色
調が5T能であり、更に〒iN、 ZrN、 HfN、
TaNSTag、 N’bOの中から選ばれた1糧以
上が含有していると一層色調のコントロールがeF易で
ある。Ti, which is the main component of the hard phase contained in the sintered alloy of the present invention
For O, the ratio of T1 element to 0 element does not have to be 1:l, and even if there is a slight change in color tone due to increase or decrease of 0 element, the O element can be controlled within a stable range as low grade acclimatized titanium. A constant color tone can be obtained by controlling the bonding phase cover and type, and furthermore, 〒iN, ZrN, HfN,
If one or more selected from TaNSTag and N'bO is contained, the color tone can be controlled even more easily.
本発明の焼結合金の硬質相中に窪化物、縦化物が含有し
ているときは、TiOがTiN、 ZrN、 HfM。When the hard phase of the sintered alloy of the present invention contains indentations or verticalizations, TiO is TiN, ZrN, or HfM.
TaN%Tag、 NbCの中から選ばれた1種以上と
のは窟化物、酸炭化物、酸炭窒化物の固溶体としてもお
よび/また1jTioと窒化匍、炭化物又は炭窒化物と
の混合物として存在しても良い。TaN%Tag, NbC may exist as a solid solution of oxides, oxycarbides, oxycarbonitrides, and/or as a mixture of 1jTio and nitrides, carbides, or carbonitrides. It's okay.
本発明の焼結合金は、真空中又は不活性気流中で常圧の
普通焼結によっても得られるし1.ポットプレス法によ
っても得られる。更に必要ならは、緻密性を高めるため
に■工P処理を行なうことも装飾品用部材としての効果
が有る。The sintered alloy of the present invention can also be obtained by ordinary sintering in vacuum or in an inert gas flow at normal pressure.1. It can also be obtained by the pot press method. Furthermore, if necessary, it is also effective as a member for decorative articles to perform a P treatment to increase the density.
次に本発明の焼結合金に於て数値限定した理由について
述べる。Next, the reason for numerically limiting the sintered alloy of the present invention will be described.
(1)結合相の含有量
結合相含有量が2重重チ禾満では、相対的に@II!質
相量が98重量−を越えて多くなり、硬質相蓋が多いと
焼結性及び緻密性が低下する。又、結合相量が60重量
−を越えて多くなると、相対的に硬質相が40重it−
未満となり、焼結中の変形が大きくなり後工程の作業4
間が多くなるために結合相量は、2重を一〜60重量−
と決めた。(1) Binding phase content If the binding phase content is double-layered, it is relatively @II! If the amount of solid phase exceeds 98% by weight and the amount of hard phase is large, sinterability and compactness will decrease. Furthermore, when the amount of binder phase increases beyond 60% by weight, the hard phase becomes relatively 40% by weight.
As a result, deformation during sintering becomes large and post-process work 4 is required.
Since the space between the layers increases, the amount of binder phase should be 1 to 60% by weight.
I decided.
(2)結合相と置換する金属の量
Ti、Zr、 Hf、 V、Nb%Ta、 W、 Or
。(2) Amount of metal replacing binder phase Ti, Zr, Hf, V, Nb%Ta, W, Or
.
Mo、 At、 81、Mn、Ou、Bの中から選ばれ
たl種以上の金属と結合相と置換す、るのが結合相に対
して0.5重量−未満では、耐食性及び同浴強度の効果
が弱く、40重量−を越えて多くなると焼結性及び緻密
性が低下する几めに結合相と置換する一金属の量は結合
相に対゛してα5〜40重量−と決めた。If the binder phase is replaced with one or more metals selected from Mo, At, 81, Mn, Ou, and B, if the amount is less than 0.5% by weight relative to the binder phase, the corrosion resistance and bath strength will be reduced. The effect is weak, and if the amount exceeds 40% by weight, the sinterability and compactness will deteriorate, so the amount of one metal to be substituted for the binder phase was determined to be α5 to 40% by weight relative to the binder phase. .
(3)結合相と置換する酸化物
Altoz、 YzOs、Zr01、MfOの中から選
ばれた1棟以上の酸化物を、結合相と置換するのが結合
相に対してα5重量−未満では、分散強化及び耐食性の
効果が弱く、25重*S+越えて多くなると焼結性及び
緻密性が低下するために結合相と置換する酸化物量は結
合相に対して0.5〜25重itチと決めた。(3) Oxide to replace the binder phase If the binder phase is replaced with one or more oxides selected from Altoz, YzOs, Zr01, and MfO, if the binder phase is less than α5 weight, the dispersion The effect of strengthening and corrosion resistance is weak, and if the amount exceeds 25*S+, the sinterability and compactness will decrease, so the amount of oxide to be replaced with the binder phase is determined to be 0.5 to 25*S+. Ta.
以下に本発明〇−帖金合金実施例に従って具体的に説明
する。The present invention will be specifically explained below according to examples of the present invention.
実施例
原料粉末として、T10、TiOと他化合物との固溶体
、炭化物、雪化物、酸化物及び各樺金属粉末を準備し、
これらの原料粉末全使用して第1表のような割合に各試
料を配合し、これにパラフィンとア七トンを加えてボー
ルミルにより粉砕混合した後乾燥した。この混合粉末を
2 t/ad の加圧力で成形し、10−1〜1O−
4關Hf真空中1250〜1500℃の各温度又はポッ
トプレスによって焼結し、更に、必要に応じてHIP処
理を行つ比。焼結体は、ダイヤモンド砥石により鏡面研
摩し、色調及び硬度を調べてその結果′Ik:第1表に
示した。As example raw material powders, T10, a solid solution of TiO and other compounds, carbide, snowride, oxide, and each birch metal powder were prepared,
All of these raw material powders were used to formulate each sample in the proportions shown in Table 1, and paraffin and amethane were added thereto, pulverized and mixed in a ball mill, and then dried. This mixed powder was molded with a pressure of 2 t/ad to form a powder of 10-1 to 1O-
Sintering is performed at various temperatures of 1250 to 1500°C in a 4-Hf vacuum or by a pot press, and further subjected to HIP treatment if necessary. The sintered body was mirror-polished using a diamond grindstone, and its color tone and hardness were examined and the results are shown in Table 1: 'Ik'.
\
\
\
ゝ゛\
第1表
本発明の焼結合金は、第1表に示した色調及び硬度から
装飾品用部材とし・ての優れた%性の有ることが確認で
き念。更に、第1表の硬さ%性から切削工具、耐摩耗工
具等の工具としても使用可能であることが推測できる。\ \ \ ゝ゛\ Table 1 From the color tone and hardness shown in Table 1, it can be confirmed that the sintered alloy of the present invention has excellent percent properties as a member for decorative articles. Furthermore, from the hardness percentage shown in Table 1, it can be inferred that it can be used as a cutting tool, a wear-resistant tool, etc.
Claims (1)
合相2〜60重tSと残りTiOから成る硬質相と不可
避不純物であることt−特徴とする酸化チタン基有色焼
結合金。 (2)上記結合相の1i′t−咳結合相に対してT1、
Zr%Hf、 V、 Wb、 Ta、 W、 Or%M
o、Aj。 Sl、Mn、Cu、Bの中から選ばれた1種以上の金@
0.5〜40ムjllIlチによって置換したことt
%像とする臀許縛求の範1第1項記載の酸化チタン基有
色焼g式釜。 (3)上記結合相の1部を該結合相に対してムt203
、yzos、ZrO2、MfO17)中から選ばれたI
Ir[以上の酸化物0.5〜25重量−によって置換し
たこと1に特徴とする脣許請求の範囲第1項又は第2項
記載の酸化チタン基有色焼結合金。 [41Fe、N1、coの中から遍はれfc1棟以上の
結合相2〜60重aSとTiO1〜99]ll[菫−と
Tin、ZrN、HfM、Tag%TaC,)JbCO
中から選ばれたls以上99〜IJHt−とから成る硬
質相40〜98′N菫−と不可避不純物であること1部
黴とする酸化チタン基有色焼結合金。 (5) 上記結合相の1mを該結合相に対してT1、
Zr、 Hf、 V、IN bSTa、 W%C!r、
Mo、ムt181、Mn、Cu、Bの中から選はれた
111以上の金Jg 0.5〜4・0夏it−によって
置換したことを特徴とする特許結末の範咄#!4項記載
の酸化チタン基有色焼結合金。 (6)上記結合相の1部を#結合相に対してムt201
、Y2O3、ZrO2、MOの中から適はれた1種以上
の酸化物0.5〜25重量−によって置換したこと1部
黴とする特許蹟求のafl第4項又は第5項記載の酸化
チタン基有色焼結台金。[Claims] (11) A hard phase consisting of a binder phase of 2 to 60 tS selected from 11Fe, Ni, and CO and the remainder TiO, and a titanium oxide group characterized by unavoidable impurities. Colored sintered alloy. (2) T1 for the 1i't-cough bonding phase of the above bonding phase,
Zr%Hf, V, Wb, Ta, W, Or%M
o, Aj. One or more types of gold selected from Sl, Mn, Cu, and B@
It was replaced by 0.5 to 40 mm.
A titanium oxide-based colored sintering kettle according to item 1 of category 1 for determining the butt tolerance as a percentage image. (3) Mut203 a part of the above bonded phase to the bonded phase.
, yzos, ZrO2, MfO17)
A titanium oxide-based colored sintered alloy according to claim 1 or 2, characterized in that the titanium oxide-based colored sintered alloy is substituted with 0.5 to 25% by weight of an oxide of Ir. [41Fe, N1, co, fc1 or more bonded phase 2-60 aS and TiO1-99]ll [violet and Tin, ZrN, HfM, Tag% TaC,) JbCO
A titanium oxide-based colored sintered alloy comprising a hard phase of 40 to 98'N violet selected from the group consisting of ls or more of 99 to IJHt and partly mold as an inevitable impurity. (5) 1 m of the above bonded phase is T1 to the bonded phase,
Zr, Hf, V, IN bSTa, W%C! r,
Patent ending range # that is characterized by being replaced by 111 or more gold Jg 0.5 to 4.0 summer it- selected from Mo, Mut181, Mn, Cu, and B! 4. The titanium oxide-based colored sintered alloy according to item 4. (6) Add a part of the above bonded phase to the #bond phase.
, Y2O3, ZrO2, MO, the oxidation described in the AFL paragraph 4 or 5 of the patent application, in which 1 part mold is substituted with 0.5 to 25% by weight of one or more oxides selected from among , Y2O3, ZrO2, MO. Titanium-based colored sintered base metal.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18822081A JPS5891145A (en) | 1981-11-24 | 1981-11-24 | Titanium oxide-base colored sintered alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18822081A JPS5891145A (en) | 1981-11-24 | 1981-11-24 | Titanium oxide-base colored sintered alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5891145A true JPS5891145A (en) | 1983-05-31 |
JPH0258335B2 JPH0258335B2 (en) | 1990-12-07 |
Family
ID=16219863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18822081A Granted JPS5891145A (en) | 1981-11-24 | 1981-11-24 | Titanium oxide-base colored sintered alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5891145A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007039752A (en) * | 2005-08-04 | 2007-02-15 | National Institute Of Advanced Industrial & Technology | Tool or mold material in which a hard film is formed on a hard alloy for forming a high-hardness film, and a method for producing the same |
JP2007524758A (en) * | 2003-05-20 | 2007-08-30 | エクソンモービル リサーチ アンド エンジニアリング カンパニー | High performance corrosion resistant-corrosive boride cermet |
CN104233282A (en) * | 2013-06-20 | 2014-12-24 | 沈阳大陆激光技术有限公司 | Nickel base alloy powder for repairing turbocharger wheel disc of internal combustion engine |
CN113416862A (en) * | 2021-06-04 | 2021-09-21 | 合肥工业大学 | Preparation method of hard alloy and hard alloy prepared by adopting same |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS501008A (en) * | 1973-05-09 | 1975-01-08 |
-
1981
- 1981-11-24 JP JP18822081A patent/JPS5891145A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS501008A (en) * | 1973-05-09 | 1975-01-08 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007524758A (en) * | 2003-05-20 | 2007-08-30 | エクソンモービル リサーチ アンド エンジニアリング カンパニー | High performance corrosion resistant-corrosive boride cermet |
JP2007039752A (en) * | 2005-08-04 | 2007-02-15 | National Institute Of Advanced Industrial & Technology | Tool or mold material in which a hard film is formed on a hard alloy for forming a high-hardness film, and a method for producing the same |
CN104233282A (en) * | 2013-06-20 | 2014-12-24 | 沈阳大陆激光技术有限公司 | Nickel base alloy powder for repairing turbocharger wheel disc of internal combustion engine |
CN113416862A (en) * | 2021-06-04 | 2021-09-21 | 合肥工业大学 | Preparation method of hard alloy and hard alloy prepared by adopting same |
Also Published As
Publication number | Publication date |
---|---|
JPH0258335B2 (en) | 1990-12-07 |
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