JPH0723530B2 - Decorative Au alloy member having surface hardened layer - Google Patents

Decorative Au alloy member having surface hardened layer

Info

Publication number
JPH0723530B2
JPH0723530B2 JP16661886A JP16661886A JPH0723530B2 JP H0723530 B2 JPH0723530 B2 JP H0723530B2 JP 16661886 A JP16661886 A JP 16661886A JP 16661886 A JP16661886 A JP 16661886A JP H0723530 B2 JPH0723530 B2 JP H0723530B2
Authority
JP
Japan
Prior art keywords
alloy
hardened layer
decorative
alloy member
hardened
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
Application number
JP16661886A
Other languages
Japanese (ja)
Other versions
JPS6324051A (en
Inventor
秀昭 吉田
正樹 森川
利玄 臂
福久 松田
一博 中田
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.)
Mitsubishi Materials Corp
Original Assignee
Mitsubishi Materials Corp
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 Mitsubishi Materials Corp filed Critical Mitsubishi Materials Corp
Priority to JP16661886A priority Critical patent/JPH0723530B2/en
Publication of JPS6324051A publication Critical patent/JPS6324051A/en
Publication of JPH0723530B2 publication Critical patent/JPH0723530B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、すぐれた表面硬さを有し、特に指輪、ネッ
クレス等の装飾品として用いるのに適した、窒化処理に
よる表面硬化層を有するAu合金部材に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention has a surface hardened layer by nitriding treatment, which has excellent surface hardness and is particularly suitable for use as a decorative article such as a ring or a necklace. It relates to an Au alloy member.

〔従来の技術〕[Conventional technology]

周知のように、金はすべての金属中化学的に最も安定し
た金属で、永く美麗な黄金色を保持できる上に、物理的
にはきわめて柔軟で、あらゆる金属中展延性にもっとも
すぐれ、細工が容易であるところから、金ならびにAu合
金は古来より装飾用材料として広く利用されてきた。
As is well known, gold is the most chemically stable metal of all metals, retains a beautiful golden color for a long time, is physically very flexible, and has the best malleability in all metals Since it is easy, gold and Au alloys have been widely used as decorative materials since ancient times.

純金はきわめて軟かくて傷つきやすいため、これにAg,C
u等を添加して適度の硬さをもたせた、いわゆる18K、14
K等のAu合金が一般に装飾用材料として利用されている
が、このようなAu合金でも装飾品として身につけたとき
にはなお傷がつきやすいという欠点を有する。
Pure gold is extremely soft and easily damaged, so Ag, C
So-called 18K, 14 with appropriate hardness by adding u, etc.
Au alloys such as K are generally used as a decorative material, but even such an Au alloy has a drawback that it is still easily scratched when worn as a decorative article.

また、近年ダイヤカット法といわれる鋭い切込みによる
鮮明な模様をほどこしたAu合金の指輪、ネックレス等が
普及してきたが、従来のAu合金では軟質のためエッジが
摩耗し、模様が不鮮明になることが屡々問題となってお
り、このような問題を克服するためにAu合金を硬くする
工夫が種々試みられている。
In recent years, Au alloy rings, necklaces, etc. that have a sharp pattern called a diamond cut method with a sharp cut have become popular, but in conventional Au alloy, the edge is worn and the pattern becomes unclear due to its softness. This is often a problem, and various attempts have been made to harden the Au alloy in order to overcome such problems.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

一方、Au合金を装飾品として身につけたとき、その表面
に傷がつかないためには、通常Au合金部材の硬さがHv
(ビッカース硬さ):350以上、好ましくはHv:500以上が
よいとされており、例えば腕時計の文字盤ガラスの硬さ
はおよそHv:500であるから、Hv:500以上のAu合金ができ
れば、この文字盤ガラスでも傷がつかない硬い装飾用の
Au合金部材が提供できることになる。
On the other hand, when the Au alloy is worn as a decorative item, the hardness of the Au alloy member is usually Hv so that the surface is not scratched.
(Vickers hardness): 350 or more, preferably Hv: 500 or more is said to be good, for example, the hardness of the watch face glass is about Hv: 500, so if Hv: 500 or more Au alloy can be made, A hard decorative piece that won't get scratched even with this dial glass
Au alloy members can be provided.

しかしながら、今のところ、種々のAu合金に熱処理を施
し、あるいはさらに加工硬化を利用しても、その硬さは
精々Hv:300どまりであって、上記のような要求を満たす
Au合金の開発には成功していないのが現状である。
However, at present, even if various Au alloys are subjected to heat treatment or further work hardening, the hardness is at most Hv: 300, which satisfies the above requirements.
At present, the development of Au alloys has not been successful.

〔問題点を解決するための手段〕[Means for solving problems]

そこで、本発明者等は、上述のような観点から、硬質、
特に高い表面硬さを有するAu合金部材を得べく研究を行
なった結果、重量%で、 Mn:5〜25%、 を含有し、さらに必要に応じて、 Ni,Co,およびFe(以下、これらを総称して鉄族金属とい
う)のうちの1種または2種以上:0.5〜20%と、 Ag,Cu,およびPdのうちの1種または2種以上:3〜35%、 のうちのいずれか、または両方を含有し、残りがAuと不
可避不純物からなる組成を有するAu合金を基体部材と
し、これの表面に窒化処理を施すと、表面より拡散侵入
したNが、合金成分としてのMnと窒化マンガン、さらに
Mnおよび鉄族金属と複合窒化物を形成して、ビッカース
硬さで500上を有する表面硬化層が形成されるようにな
るという知見を得たのである。
Therefore, the present inventors, from the above viewpoint, hard,
As a result of research to obtain an Au alloy member having a particularly high surface hardness, as a result, it contains Mn in an amount of 5 to 25% by weight and, if necessary, Ni, Co, and Fe (hereinafter, these Are collectively referred to as iron group metals), 0.5 to 20%, and 1 or 2 or more of Ag, Cu, and Pd: 3 to 35%. Or both are contained and the rest is made of an Au alloy having a composition of Au and inevitable impurities, and when the surface of the base member is subjected to nitriding treatment, N diffused and infiltrated from the surface becomes Mn as an alloy component. Manganese nitride,
They have found that a complex nitride is formed with Mn and an iron group metal to form a surface hardened layer having a Vickers hardness of 500 or more.

この発明は、上記知見にもとづいてなされたものであっ
て、以下にAu合金基体の成分組成範囲を上記の通りに限
定した理由を説明する。
The present invention has been made based on the above findings, and the reason why the component composition range of the Au alloy substrate is limited as described above will be described below.

(a)Mn Mn成分は、窒化処理に際して、窒化マンガン、さらに同
じく必要により合金成分として含有させた鉄族金属と共
に、複合窒化物を形成し、もってAu合金基体の表面に、
ビッカース硬さで500以上の高硬度を有する窒化処理表
面硬化層を形成するのに不可欠な成分であるが、その含
有量が5%未満では所望の高硬度をもった表面硬化層を
形成することができず、一方25%を越えて含有させる
と、窒化処理表面硬化層に剥離現象が現われるようにな
ることから、その含有量を5〜25%と定めた。
(A) Mn Mn component forms a composite nitride together with manganese nitride and an iron group metal which is also contained as an alloy component if necessary during the nitriding treatment, and thus, on the surface of the Au alloy substrate,
It is an essential component for forming a nitriding surface-hardened layer with a Vickers hardness of 500 or higher, but if the content is less than 5%, a surface-hardened layer with the desired high hardness should be formed. However, if the content exceeds 25%, a peeling phenomenon will appear in the nitriding surface-hardened layer, so the content was defined as 5 to 25%.

(b)鉄族金属 これらの成分には、Mnと複合窒化物を形成して高硬度の
窒化処理表面硬化層を形成するほか、Au合金基体の強度
を向上させる作用があるので、これらの特性が要求され
る場合に必要に応じて含有されるが、その含有量が0.5
%未満では、所望の高強度を確保することができないば
かりでなく、所望の硬さ向上効果が得られず、一方20%
を越えて含有させると、Auのもつすぐれた特性を十分に
発揮することができなくなることから、その含有量を0.
5〜20%と定めた。
(B) Iron group metal These components have the function of forming a composite nitride with Mn to form a high-hardness nitriding surface-hardened layer and also improving the strength of the Au alloy substrate. If required, it is contained as necessary, but the content is 0.5
If it is less than 20%, not only the desired high strength cannot be secured, but also the desired hardness improvement effect cannot be obtained, while 20%
If it is contained in excess of 10%, it will not be possible to fully exhibit the excellent properties of Au, so its content should be 0.
It was set at 5 to 20%.

(c)Ag,Cu,およびPd これらの成分には、素地に固溶して、これを固溶強化す
る作用があるので、さらに一段の強度が要求される場合
に必要に応じて含有されるが、その含有量が3%未満で
は所望の強度向上効果が得られず、一方35%を越えて含
有させると、Auのもつ特性を十分に発揮することができ
なくなることから、その含有量を3〜35%と定めた。
(C) Ag, Cu, and Pd These components have the action of forming a solid solution in the base material and strengthening the solid solution, so if further strength is required, they are contained as necessary. However, if the content is less than 3%, the desired strength-improving effect cannot be obtained. On the other hand, if the content exceeds 35%, the characteristics possessed by Au cannot be fully exhibited, so the content is It was set at 3 to 35%.

なお、この発明のAu合金基体の溶解に際して、脱酸剤と
してCdやZnなどを使用する場合があるが、それぞれ3%
以下の含有ならば、前記基体の特性が何ら損なわれるも
のではない。
When melting the Au alloy substrate of the present invention, Cd, Zn or the like may be used as a deoxidizing agent.
The following contents do not impair the characteristics of the substrate.

この発明のAu合金部材の製造に際して適用される窒化処
理、特にイオン窒化処理は次のようにして実施される。
すなわち、 0.5〜10Torrの内部圧力となるように、H2とN2との混
合ガスまたはNH3ガスを導入した密閉容器内に、窒化処
理を施すべきAu合金基体を陰極として封入し、この陰極
と、別に封入された陽極との間に100〜1500Vの電圧を印
加してグロー放電を発生させることによって行なわれ、
この結果前記放電によってイオン化された雰囲気中の窒
素がAu合金基体(陰極)に衝突して、そのイオンのもつ
高い運動エネルギーによりAu合金基体が加熱され、その
表面のイオン窒化処理が達成されるようになるのであ
る。
The nitriding treatment applied in the production of the Au alloy member of the present invention, particularly the ion nitriding treatment, is carried out as follows.
That is, an Au alloy substrate to be subjected to nitriding treatment is enclosed as a cathode in a closed container into which a mixed gas of H 2 and N 2 or NH 3 gas is introduced so that the internal pressure is 0.5 to 10 Torr. By applying a voltage of 100 to 1500 V between the separately enclosed anode and the anode, a glow discharge is generated,
As a result, the nitrogen in the atmosphere ionized by the discharge collides with the Au alloy substrate (cathode), and the high kinetic energy of the ions heats the Au alloy substrate so that the surface is ion-nitrided. It becomes.

〔実施例〕〔Example〕

つぎに、この発明のAu合金部材を実施例により説明す
る。
Next, the Au alloy member of the present invention will be described with reference to examples.

TIGアークを用い、銅製水冷るつぼ内で、必要な添加金
属と電解Auを溶解して、それぞれ第1表に示される成分
組成をもったAu合金溶湯:10gを調製した後、ボタン・イ
ンゴットに金型鋳造し、このインゴットを表面研磨して
寸法: 10mm×1mmを有する試験片(Au合金基体)とし、この
試験片の一部を用いて強度を評価する目的で抗折力を測
定すると共に、マイクロビッカース硬さを測定した後、
さらに、5Torrの圧力を有するN2とH2との混合ガス
(混合比1:1)雰囲気中、温度:830℃で5時間の条件に
てイオン窒化処理を施すことによって、本発明Au合金部
材1〜16、および基体の組成が従来Au合金に相当する組
成を有する比較Au合金部材1〜3をそれぞれ製造した。
Using a TIG arc, in a copper water-cooled crucible, the required additional metals and electrolytic Au are melted to prepare 10 g of Au alloy melt having the composition shown in Table 1, respectively, and then gold is placed on the button ingot. Die casting, surface polishing this ingot and dimensions: As a test piece (Au alloy substrate) having a size of 10 mm × 1 mm, after measuring the transverse rupture force for the purpose of evaluating the strength using a part of this test piece, after measuring the micro Vickers hardness,
Furthermore, the Au alloy member of the present invention is subjected to an ion nitriding treatment in a mixed gas atmosphere (mixing ratio 1: 1) of N 2 and H 2 having a pressure of 5 Torr at a temperature of 830 ° C. for 5 hours. 1 to 16 and comparative Au alloy members 1 to 3 each having a composition of the substrate corresponding to that of the conventional Au alloy were manufactured.

ついで、この結果得られた各種の部材について、その表
面最高硬さを、マイクロビッカースにより測定した。こ
れらの測定結果を第1表に合わせて示した。
Then, the maximum surface hardness of each of the various members obtained as a result was measured by micro-Vickers. The results of these measurements are also shown in Table 1.

〔発明の効果〕 第1表に示される結果から、本発明のAu合金部材1〜16
は、いずれも窒化処理により表面硬さの格段の向上が得
られたのに対し、比較Au合金部材1,2(18K合金および14
K合金)では、窒化処理によっても、その表面硬さは殆
んど変らず、さらに硬質Au合金で構成された比較Au合金
部材3においても殆ど硬さの向上が得られないことが明
らかである。
[Effects of the Invention] From the results shown in Table 1, the Au alloy members 1 to 16 of the present invention were obtained.
In both cases, the surface hardness was significantly improved by nitriding treatment, while the comparative Au alloy members 1, 2 (18K alloy and 14K alloy
It is clear that the surface hardness of (K alloy) is hardly changed by the nitriding treatment, and that the hardness of the comparative Au alloy member 3 made of the hard Au alloy is hardly improved. .

上述のように、この発明のAu合金部材は、特に窒化処理
により形成された著しく硬い表面硬化層を有するので、
これらの特性が要求される装飾用部材として使用した場
合にきわめて長期に亘ってすぐれた性能を発揮するもの
である。
As described above, since the Au alloy member of the present invention has a remarkably hard surface-hardened layer formed by the nitriding treatment,
When used as a decorative member that requires these properties, it exhibits excellent performance for an extremely long period of time.

フロントページの続き (72)発明者 中田 一博 大阪府大阪市阿倍野区阪南町1−35−16Continued Front Page (72) Inventor Kazuhiro Nakata 1-35-16 Hannan-cho, Abeno-ku, Osaka-shi, Osaka

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】Mu:5〜25%、 を含有し、残りがAuと不可避不純物からなる組成(以上
重量%)を有するAu合金基体の表面に、窒化マンガンに
よって硬化された窒化処理表面硬化層を形成してなる装
飾用Au合金部材。
1. A nitriding surface-hardened layer which is hardened by manganese nitride on the surface of an Au alloy substrate containing Mu: 5 to 25%, and the balance of which is a composition of Au and unavoidable impurities (above wt%). A decorative Au alloy member formed by forming.
【請求項2】Mu:5〜25%、 Ni,Co,およびFe(以下鉄族金属という)のうちの1種ま
たは2種以上:0.5〜20%、 を含有し、残りがAuと不可避不純物からなる組成(以上
重量%)を有するAu合金基体の表面に、Muと、鉄族金属
の複合窒素化物によって硬化された窒化処理表面硬化層
を形成してなる装飾用Au合金部材。
2. Mu: 5 to 25%, one or more of Ni, Co, and Fe (hereinafter referred to as iron group metals): 0.5 to 20%, with the balance being Au and inevitable impurities. An Au alloy member for decoration, which is formed by forming a nitriding surface hardened layer which is hardened by a composite nitride of an iron group metal and Mu on the surface of an Au alloy substrate having a composition (at least by weight).
【請求項3】Mu:5〜25%、 を含有し、さらに、 Ag,Cu,およびPdのうちの1種または2種以上:3〜35%、 を含有し、残りがAuと不可避不純物からなる組成(以上
重量%)を有するAu合金基体の表面に、窒化マンガンに
よって硬化された窒化処理表面硬化層を形成してなる装
飾用Au合金部材。
3. A glass containing Mu: 5 to 25%, further containing one or more of Ag, Cu, and Pd: 3 to 35%, and the rest containing Au and inevitable impurities. An Au alloy member for decoration, comprising a surface of an Au alloy substrate having the following composition (at least by weight) and a nitriding surface hardened layer hardened by manganese nitride.
【請求項4】Mu:5〜25%、 Ni,Co,およびFe(以下鉄族金属という)のうちの1種ま
たは2種以上:0.5〜20%、 を含有し、さらに、 Ag,Cu,およびPdのうちの1種または2種以上:3〜35%、 を含有し、残りがAuと不可避不純物からなる組成(以上
重量%)を有するAu合金基体の表面に、Muと鉄族金属の
複合窒化物によって硬化された窒化処理表面硬化層を形
成してなる装飾用Au合金部材。
4. Mu: 5 to 25%, one or more of Ni, Co, and Fe (hereinafter referred to as iron group metal): 0.5 to 20%, further containing Ag, Cu, One or more of Pd and Pd: 3 to 35%, and the balance of Au and unavoidable impurities in the composition of the Au alloy substrate. A decorative Au alloy member formed by forming a nitriding surface-hardened layer hardened by a composite nitride.
JP16661886A 1986-07-17 1986-07-17 Decorative Au alloy member having surface hardened layer Expired - Lifetime JPH0723530B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16661886A JPH0723530B2 (en) 1986-07-17 1986-07-17 Decorative Au alloy member having surface hardened layer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16661886A JPH0723530B2 (en) 1986-07-17 1986-07-17 Decorative Au alloy member having surface hardened layer

Publications (2)

Publication Number Publication Date
JPS6324051A JPS6324051A (en) 1988-02-01
JPH0723530B2 true JPH0723530B2 (en) 1995-03-15

Family

ID=15834641

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16661886A Expired - Lifetime JPH0723530B2 (en) 1986-07-17 1986-07-17 Decorative Au alloy member having surface hardened layer

Country Status (1)

Country Link
JP (1) JPH0723530B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2614780B2 (en) * 1990-08-03 1997-05-28 富士電気化学 株式会社 Manufacturing method of optical isolator
JP2001335861A (en) * 2000-05-26 2001-12-04 Tokuriki Honten Co Ltd Gold alloy for ornament
JP2001335860A (en) * 2000-05-26 2001-12-04 Tokuriki Honten Co Ltd Gold alloy for ornament
FR2815044B1 (en) * 2000-10-06 2003-03-21 Cookson Metaux Precieux Sa 18K GRAY GOLD ALLOY FOR JEWELERY, NICKEL FREE AND PALLADIUM FREE
CN109811176A (en) * 2019-03-25 2019-05-28 杭州辰卓科技有限公司 A kind of electron device package high-damping bonding line billon and its technique

Also Published As

Publication number Publication date
JPS6324051A (en) 1988-02-01

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