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JPS5891145A - Titanium oxide-base colored sintered alloy - Google Patents

Titanium oxide-base colored sintered alloy

Info

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
Application number
JP18822081A
Other languages
Japanese (ja)
Other versions
JPH0258335B2 (en
Inventor
Mikio Fukuhara
幹夫 福原
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tungaloy Corp
Original Assignee
Toshiba Tungaloy Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toshiba Tungaloy Co Ltd filed Critical Toshiba Tungaloy Co Ltd
Priority to JP18822081A priority Critical patent/JPS5891145A/en
Publication of JPS5891145A publication Critical patent/JPS5891145A/en
Publication of JPH0258335B2 publication Critical patent/JPH0258335B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a colored sintered alloy for decorative articles having a light weight, a beautiful golden color and high hardness by consisting the same of specific ratios of a bound phase of Fe, Ni, Co and a hard phase of TiO. CONSTITUTION:A sintered alloy consisting of a hard phase of TiO having a beautiful golden color and characteristics of high hardness 2-60wt% a bound phase of >=1 kind among Fe, Ni, Co which are effective in improving wettability with said phase, strength, sinterability and compactness, and unavoidable impurities. If necessary, a part of said bound phase may be substituted with about 0.5-40wt% >=1 kind among Ti, Zr, Hf, V, Nb, Ta, W, Cr, Mo, Al, Si, Mn, Cu, B in order to improve sinterability, corrosion resistance and the solid soln. of the bound phase. If the bound phase is below the lower limit, sinterability compactness degrade and in excess of the upper limit, the deformation during sintering increases and the working time in pose stages increases. If the substituting metals such as Ti are below the lower limit, the effect of the corrosion resistance and the strength of the solid soln. is weak and in excess of the upper limit, the sinterability and compactness degrade.

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)

【特許請求の範囲】 (11Fe、Ni、COの中から選ばれた1種以上の結
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.
JP18822081A 1981-11-24 1981-11-24 Titanium oxide-base colored sintered alloy Granted JPS5891145A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS501008A (en) * 1973-05-09 1975-01-08

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS501008A (en) * 1973-05-09 1975-01-08

Cited By (4)

* Cited by examiner, † Cited by third party
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

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