JPS622031B2 - - Google Patents
Info
- Publication number
- JPS622031B2 JPS622031B2 JP58217471A JP21747183A JPS622031B2 JP S622031 B2 JPS622031 B2 JP S622031B2 JP 58217471 A JP58217471 A JP 58217471A JP 21747183 A JP21747183 A JP 21747183A JP S622031 B2 JPS622031 B2 JP S622031B2
- Authority
- JP
- Japan
- Prior art keywords
- alloy member
- alloy
- hardness
- hardened
- rare earth
- 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
Links
- 229910001020 Au alloy Inorganic materials 0.000 claims description 24
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 9
- 229910052802 copper Inorganic materials 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 229910052726 zirconium Inorganic materials 0.000 claims description 6
- 239000012535 impurity Substances 0.000 claims description 5
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910052737 gold Inorganic materials 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 229910052748 manganese Inorganic materials 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 235000019646 color tone Nutrition 0.000 description 12
- 230000000694 effects Effects 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 239000010949 copper Substances 0.000 description 4
- 239000010931 gold Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000006104 solid solution Substances 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 1
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910004835 Na2B4O7 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 238000005885 boration reaction Methods 0.000 description 1
- 238000005271 boronizing Methods 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/60—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using solids, e.g. powders, pastes
- C23C8/62—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using solids, e.g. powders, pastes only one element being applied
- C23C8/68—Boronising
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/40—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions
- C23C8/42—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using liquids, e.g. salt baths, liquid suspensions only one element being applied
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Adornments (AREA)
Description
この発明は、著しく高い表面硬さを有し、した
がつて実用に際してはすぐれた耐摩耗性および耐
擦傷性を示し、かつ各種の色調を得ることができ
る表面硬化層を形成してなる表面硬化Au合金部
材に関するものである。
一般に、純金はきわめて軟かく、強度も低いこ
とから、これにAgやCuなどの成分を添加含有さ
せて適度の強度をもたせた、いわゆる18Kや14K
などのAu合金がある。
しかし、これらのAu合金を、指輪やネツクレ
スなどの装飾部品の製造に用いた場合、未だ十分
な硬さをもたないため、傷がつきやすく、また前
記装飾部品にダイヤカツト法により鮮明な模様を
施しても、エツジの摩耗が激しく、模様が不鮮明
になるものであり、さらにこれらのAu合金を、
接点や軸受、あるいは集電部材などの工業部品の
製造に用いた場合、硬さ不足が原因で、比較的短
かい使用寿命しか示さないものである。さらに、
また、その色調も黄金色から白色、および赤色を
呈する程度で、色調の種類に乏しく、色調変化を
楽しむには至つていないのが現状である。
そこで、本発明者等は、上述のような観点か
ら、色調はともかく、特に耐摩耗性および耐擦傷
性にすぐれたAu合金部材を開発すべく研究を行
なつた結果、重量%で(以下%はすべて重量%を
示す)、
Yおよび希土類元素のうちの1種または2種以
上:0.3〜15%、
ZrおよびAlのうちの1種または2種:0.1〜5
%、を含有し、さらに必要に応じて、
(A) Ni、Co、Cr、Fe、Mn、およびVのうちの
1種または2種以上:0.1〜20%、
(B) Cu、Ag、およびPdのうちの1種または2種
以上:1〜30%、
以上(A)〜(B)のうちの1種または2種を含有し、
残りがAuと不可避不純物からなる組成を有する
Au合金部材の表面にほう化処理を施すと、表面
より拡散侵入したBと合金成分として含有するY
および希土類元素とのほう化物を主体とした表面
硬化層が形成されるようになり、この表面硬化層
は、ビツカース硬さで500以上の高硬度を有する
ほか、その色調もほう化物の種類によつて紫紅
色、青紫色、および青色を示すことから、実用に
際してはすぐれた耐摩耗性および耐擦傷性を示
し、かつ色調が多様化するようになるという知見
を得たのである。
この発明は、上記知見にもとづいてなされたも
のであつて、以下にAu合金部材の成分組成を上
記の通りに限定した理由を説明する。
(a) Yおよび希土類元素
これらの成分は、素地に固溶するが、ほう化
処理に際しては表面より拡散したBと結合し、
ほう化物を主体とした表面硬化層を形成し、も
つてAu合金部材にすぐれた耐摩耗性と耐擦傷
性を付与すると共に、ほう化物の種類によつて
色調変化を付与せしめる作用があるが、その含
有量が0.3%以下では前記作用に所望の効果が
得られず、一方15%を越えて含有させると、
Auとの金属間化合物が多量に形成されるよう
になつてAu合金部材自体が脆化するようにな
ることから、その含有量を0.3〜15%と定め
た。
(b) ZrおよびAl
これらの成分には、脱酸作用があるほか、ほ
う化物を微細化し、かつ表面硬化層の素地に対
する密着性を向上させる作用があるが、その含
有量が0.1%未満では前記作用に所望の効果が
得られず、一方5%を越えて含有させると、部
材の加工性が劣化するようになることから、そ
の含有量を0.1〜5%と定めた。なお、これら
を総称して密着性向上成分という。
(c) Ni、Co、Cr、Fe、Mn、およびV
これらの成分は、いずれも素地に固溶し、こ
れを固溶強化すると共に、自身もほう化処理に
際して、ほう化物を形成し、表面硬化層の硬さ
をより一層向上させる作用があるので、部材の
強度並びに表面硬化層の硬さをさらに一段と向
上させる必要がある場合に選択的に含有される
が、その含有量が0.1%未満では前記作用に所
望の効果が得られず、一方20%を越えて含有さ
せると、Yおよび希土類元素のほう化物により
付与される色調が損なわれ、銀白色化するよう
になることから、その含有量を0.1〜20%と定
めた。なお、これらの成分を総称して強度・表
面硬さ向上成分という。
(d) Cu、Ag、およびPd
これらの成分には、素地に固溶して、これを
固溶強化すると作用があるので、部材の強度に
より一段の向上が必要とされる場合に選択的に
含有されるが、その含有量が1%未満では所望
の強度向上効果が得られず、一方30%を越えて
含有させると耐食性が劣化するようになること
から、その含有量を1〜30%と定めた。なお、
これらを総称して強度向上成分という。
なお、この発明のAu合金部材の溶解に際し
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、前記部
材の特性が何ら損なわれるものではない。
つぎに、この発明の表面硬化Au合金部材を実
施例により具体的に説明する。
実施例
TIGアークを用い、銅製水冷るつぼ内で、必要
な合金化金属と電解Auを配合し、溶解して、そ
れぞれ第1表に示される成分組成をもつたAu合
金溶湯:10gづつを調製した後、金型に鋳造して
ボタン状鋳片とし、ついでこの鋳片に表面研磨を
施して直経:10mmφ×厚さ:1mmの寸法を有する
チツプ材とし、このチツプ材に、予め黒鉛るつぼ
内で加熱溶融して750℃に保持してある溶融フラ
ツクス(B4C:80%、H3PO3:10%、Na2B4O7:
10%からなる組成を有する)中に24時間浸漬のほ
う化処理を施し、大気中に取出すことによつて本
発明表面硬化Au合金チツプ材1〜22をそれぞれ
製造した。
また、比較の目的で、成分組成を第1表に示さ
This invention has a surface hardening layer that has extremely high surface hardness, and therefore exhibits excellent abrasion resistance and scratch resistance in practical use, and is capable of obtaining various color tones. This relates to Au alloy members. In general, pure gold is extremely soft and has low strength, so it is made by adding ingredients such as Ag and Cu to give it a suitable strength, so-called 18K and 14K.
There are Au alloys such as However, when these Au alloys are used to manufacture decorative parts such as rings and necklaces, they are easily scratched because they do not yet have sufficient hardness, and it is difficult to create clear patterns on the decorative parts using the diamond cutting method. Even if these Au alloys are used, the edges will be severely worn and the pattern will become unclear.
When used in the manufacture of industrial parts such as contacts, bearings, or current collecting members, they have a relatively short service life due to their lack of hardness. moreover,
In addition, the color tones range from golden yellow to white to red, and there is a lack of variety in color tones, making it difficult to enjoy color tone changes. Therefore, from the above-mentioned viewpoint, the present inventors conducted research to develop an Au alloy member with particularly excellent wear resistance and scratch resistance, regardless of color tone. (all indicate weight%), one or more of Y and rare earth elements: 0.3 to 15%, one or two of Zr and Al: 0.1 to 5
%, and if necessary, (A) one or more of Ni, Co, Cr, Fe, Mn, and V: 0.1 to 20%, (B) Cu, Ag, and Contains one or more of Pd: 1 to 30%, one or two of the above (A) to (B),
The remainder consists of Au and unavoidable impurities.
When the surface of an Au alloy member is subjected to boriding treatment, the B diffused in from the surface and the Y contained as an alloy component.
A hardened surface layer consisting mainly of borides and rare earth elements is formed, and this hardened surface layer has a hardness of more than 500 on the Vickers hardness scale, and its color varies depending on the type of boride. Since it exhibits purple-red, bluish-purple, and blue colors, it has been found that in practical use, it exhibits excellent abrasion resistance and scratch resistance, and that it comes in a variety of color tones. This invention has been made based on the above findings, and the reason why the composition of the Au alloy member is limited as described above will be explained below. (a) Y and rare earth elements These components form a solid solution in the base material, but during boration treatment, they combine with B diffused from the surface,
It forms a surface hardening layer mainly composed of boride, which gives the Au alloy member excellent wear resistance and scratch resistance, and also has the effect of imparting a change in color tone depending on the type of boride. If the content is less than 0.3%, the desired effect cannot be obtained, while if the content exceeds 15%,
Since a large amount of intermetallic compounds with Au are formed and the Au alloy member itself becomes brittle, its content is set at 0.3 to 15%. (b) Zr and Al In addition to having a deoxidizing effect, these components have the effect of making borides finer and improving the adhesion of the hardened surface layer to the substrate, but if their content is less than 0.1%, The desired effect cannot be obtained in the above action, and on the other hand, if the content exceeds 5%, the workability of the member will deteriorate, so the content was set at 0.1 to 5%. Note that these are collectively referred to as adhesion improving components. (c) Ni, Co, Cr, Fe, Mn, and V All of these components form a solid solution in the base material and strengthen it as a solid solution. Since it has the effect of further improving the hardness of the hardened layer, it is selectively included when it is necessary to further improve the strength of the member and the hardness of the surface hardened layer, but its content is less than 0.1%. However, if the content exceeds 20%, the color tone imparted by the boride of Y and rare earth elements will be impaired and the color will become silvery white. The amount was determined to be 0.1-20%. Note that these components are collectively referred to as strength/surface hardness improving components. (d) Cu, Ag, and Pd These components have the effect of solid solution strengthening in the base material, so they can be used selectively when further improvement in the strength of the component is required. However, if the content is less than 1%, the desired strength improvement effect cannot be obtained, while if the content exceeds 30%, corrosion resistance will deteriorate, so the content should be reduced from 1 to 30%. It was determined that In addition,
These are collectively called strength-enhancing components. Incidentally, when melting the Au alloy member of the present invention, Cd, Zn, etc. may be used as a deoxidizing agent, but if each is contained in an amount of 3% or less, the properties of the member will not be impaired in any way. Next, the surface-hardened Au alloy member of the present invention will be specifically explained using examples. Example Using a TIG arc, necessary alloying metals and electrolytic Au were mixed and melted in a water-cooled copper crucible to prepare 10 g each of molten Au alloys having the compositions shown in Table 1. After that, it is cast into a mold to make a button-shaped slab, and then the surface of this slab is polished to make a chip material with dimensions of diameter: 10 mmφ x thickness: 1 mm, and this chip material is placed in a graphite crucible in advance. Molten flux ( B4C : 80 %, H3PO3 : 10 %, Na2B4O7 :
The surface-hardened Au alloy chips 1 to 22 of the present invention were manufactured by subjecting the chips to a boronizing treatment by immersing them in a solution containing 10% (having a composition of 10%) for 24 hours, and then taking them out into the atmosphere. In addition, for the purpose of comparison, the component composition is shown in Table 1.
【表】【table】
【表】
れるものとし、かつほう化処理を施さない以外は
同一の条件にて従来Ag合金チツプ材1〜3をそ
れぞれ製造した。
この結果得られた本発明表面硬化Au合金チツ
プ材1〜22および従来Au合金チツプ材1〜3に
ついて、湯洗およびバフ研磨後、マイクロビツカ
ース計(荷重:100g)により表面硬さを測定す
ると共に、その表面色調を観察し、さらに耐食性
を評価する目的で、100時間の人工汗試験を行な
い、変色の有無を観察した。これらの結果を第1
表に示した。また、第1表には、本発明表面硬化
Au合金チツプ材1〜22のほう化処理前のビツカ
ース硬さも示した。
第1表に示される結果から、本発明表面硬化
Au合金チツプ材1〜22は、いずれもほう化処理
によつて表面硬さが著しく向上するようになり、
ビツカース硬さ(Hv)で500以上の著しく高い表
面硬さをもつようになるほか、すぐれた耐食性を
示し、かつきれいな色調を有するのに対して、合
金成分としてYおよび希土類元素を含有せず、か
つほう化処理を行なわない従来Au合金チツプ材
1〜3は表面硬さおよび耐食性とも低く、かつ装
飾的に劣る色調しか有さないことが明らかであ
る。
上述のように、この発明の表面硬化Au合金部
材は、高硬度を有するので、これを装飾部品や工
業部品などとして用いた場合には、すぐれた耐摩
耗性と耐擦傷性を示し、さらに色調に富むほか、
耐食性にもすぐれているので、装飾的価値が大き
いなど工業上有用な特性を有するのである。[Table] Conventional Ag alloy chip materials 1 to 3 were manufactured under the same conditions except that no boriding treatment was performed. After washing with hot water and buffing, the surface hardness of the surface hardened Au alloy chips 1 to 22 of the present invention and conventional Au alloy chips 1 to 3 obtained as a result is measured using a micro-Vickers meter (load: 100 g). At the same time, in order to observe the surface color tone and further evaluate the corrosion resistance, a 100-hour artificial sweat test was conducted to observe the presence or absence of discoloration. These results are the first
Shown in the table. Table 1 also shows surface hardening according to the present invention.
The Vickers hardness of Au alloy chips 1 to 22 before boriding treatment is also shown. From the results shown in Table 1, it can be seen that the surface hardening of the present invention
All of Au alloy chip materials 1 to 22 have significantly improved surface hardness through boriding treatment.
In addition to having a significantly high surface hardness of over 500 on the Vickers hardness (Hv), it also exhibits excellent corrosion resistance and a beautiful color tone, while it does not contain Y or rare earth elements as alloying components. It is clear that the conventional Au alloy chip materials 1 to 3, which were not subjected to the boriding treatment, had low surface hardness and low corrosion resistance, and had only an inferior decorative color tone. As mentioned above, the surface-hardened Au alloy member of the present invention has high hardness, so when used as decorative parts or industrial parts, it exhibits excellent wear resistance and scratch resistance, and also has a good color tone. In addition to being rich in
Since it has excellent corrosion resistance, it has industrially useful properties such as great decorative value.
Claims (1)
以上:0.3〜15%、 ZrおよびAlのうちの1種または2種:0.1〜5
%、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合金部材の表
面に、ほう化処理により形成された表面硬化層を
有してなる表面硬化Au合金部材。 2 Yおよび希土類元素のうちの1種または2種
以上:0.3〜15%、 ZrおよびAlのうちの1種または2種:0.1〜5
%、を含有し、さらに、 Ni、Co、Cr、Fe、Mn、およびVのうちの1
種または2種以上:0.1〜20%、 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合金部材の表面
に、ほう化処理により形成された表面硬化層を有
してなる表面硬化Au合金部材。 3 Yおよび希土類元素のうちの1種または2種
以上:0.3〜15%、 ZrおよびAlのうちの1種または2種:0.1〜5
%、を含有し、さらに、 Cu、Ag、およびPdのうちの1種または2種以
上:1〜30%、 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合金部材の表面
に、ほう化処理により形成された表面硬化層を有
してなる表面硬化Au合金部材。 4 Yおよび希土類元素のうちの1種または2種
以上:0.3〜15%、 ZrおよびAlのうちの1種または2種:0.1〜5
%、を含有し、さらに Ni、Co、Cr、Fe、Mn、およびVのうちの1
種または2種以上:0.1〜20%、 Cu、Ag、およびPdのうちの1種または2種以
上:1〜30%、 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合金部材の表面
に、ほう化処理により形成された表面硬化層を有
してなる表面硬化Au合金部材。[Claims] 1 One or more of Y and rare earth elements: 0.3 to 15%, One or two of Zr and Al: 0.1 to 5
%, with the remainder consisting of Au and unavoidable impurities (weight %). 2 One or more of Y and rare earth elements: 0.3 to 15%, One or two of Zr and Al: 0.1 to 5
%, and further contains one of Ni, Co, Cr, Fe, Mn, and V
A surface hardened layer formed by boriding on the surface of an Au alloy member having a composition (by weight %) containing one or more species: 0.1 to 20%, and the remainder consisting of Au and unavoidable impurities. A surface-hardened Au alloy member. 3 One or more of Y and rare earth elements: 0.3 to 15%, One or two of Zr and Al: 0.1 to 5
%, and further contains one or more of Cu, Ag, and Pd: 1 to 30%, and the remainder is Au and unavoidable impurities (weight %). A surface hardened Au alloy member having a surface hardened layer formed by boriding treatment on the surface of the alloy member. 4 One or more of Y and rare earth elements: 0.3 to 15%, One or two of Zr and Al: 0.1 to 5
%, and further contains one of Ni, Co, Cr, Fe, Mn, and V.
A composition containing one or more species: 0.1 to 20%, one or more of Cu, Ag, and Pd: 1 to 30%, and the remainder consisting of Au and unavoidable impurities (wt%) A surface hardened Au alloy member comprising a surface hardened layer formed by boriding on the surface of the Au alloy member.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21747183A JPS60110868A (en) | 1983-11-18 | 1983-11-18 | Surface hardened au alloy member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21747183A JPS60110868A (en) | 1983-11-18 | 1983-11-18 | Surface hardened au alloy member |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60110868A JPS60110868A (en) | 1985-06-17 |
JPS622031B2 true JPS622031B2 (en) | 1987-01-17 |
Family
ID=16704750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21747183A Granted JPS60110868A (en) | 1983-11-18 | 1983-11-18 | Surface hardened au alloy member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60110868A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03166327A (en) * | 1989-11-22 | 1991-07-18 | Seiko Instr Inc | Hard-facing colored gold alloy |
US6455937B1 (en) | 1998-03-20 | 2002-09-24 | James A. Cunningham | Arrangement and method for improved downward scaling of higher conductivity metal-based interconnects |
US6551872B1 (en) | 1999-07-22 | 2003-04-22 | James A. Cunningham | Method for making integrated circuit including interconnects with enhanced electromigration resistance using doped seed layer and integrated circuits produced thereby |
US6521532B1 (en) | 1999-07-22 | 2003-02-18 | James A. Cunningham | Method for making integrated circuit including interconnects with enhanced electromigration resistance |
US6441492B1 (en) | 1999-09-10 | 2002-08-27 | James A. Cunningham | Diffusion barriers for copper interconnect systems |
JP6206872B2 (en) * | 2013-08-30 | 2017-10-04 | 国立大学法人東京工業大学 | Super elastic alloy |
CN105177340B (en) * | 2014-05-16 | 2018-10-16 | 周大福珠宝金行有限公司 | microalloyed gold |
CN109234564A (en) * | 2018-10-12 | 2019-01-18 | 佛山科学技术学院 | A kind of wear-resisting rose gold plate and its preparation process |
US20240158890A1 (en) * | 2021-03-29 | 2024-05-16 | Tokyo University Of Science Foundation | Gold Alloy and Method for Producing Gold Alloy |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51139522A (en) * | 1975-05-28 | 1976-12-01 | Ishifuku Kinzoku Kogyo Kk | Au-alloy |
JPS5271330A (en) * | 1975-12-11 | 1977-06-14 | Sankin Ind Co | Goldd silverr palladium alloy having refined grains by addition of small amount of rhenium for dental castings |
JPS52115724A (en) * | 1976-03-25 | 1977-09-28 | Ishifuku Metal Ind | Gold alloy |
JPS58126946A (en) * | 1982-01-25 | 1983-07-28 | Toyota Central Res & Dev Lab Inc | Manufacture of copper alloy containing dispersed boride |
-
1983
- 1983-11-18 JP JP21747183A patent/JPS60110868A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51139522A (en) * | 1975-05-28 | 1976-12-01 | Ishifuku Kinzoku Kogyo Kk | Au-alloy |
JPS5271330A (en) * | 1975-12-11 | 1977-06-14 | Sankin Ind Co | Goldd silverr palladium alloy having refined grains by addition of small amount of rhenium for dental castings |
JPS52115724A (en) * | 1976-03-25 | 1977-09-28 | Ishifuku Metal Ind | Gold alloy |
JPS58126946A (en) * | 1982-01-25 | 1983-07-28 | Toyota Central Res & Dev Lab Inc | Manufacture of copper alloy containing dispersed boride |
Also Published As
Publication number | Publication date |
---|---|
JPS60110868A (en) | 1985-06-17 |
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