JPH02225655A - Gold alloy that is colored shiny black and its coloring method - Google Patents
Gold alloy that is colored shiny black and its coloring methodInfo
- Publication number
- JPH02225655A JPH02225655A JP1045420A JP4542089A JPH02225655A JP H02225655 A JPH02225655 A JP H02225655A JP 1045420 A JP1045420 A JP 1045420A JP 4542089 A JP4542089 A JP 4542089A JP H02225655 A JPH02225655 A JP H02225655A
- Authority
- JP
- Japan
- Prior art keywords
- gold
- alloy
- weight
- atmosphere
- pure
- 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.)
- Pending
Links
- 229910001020 Au alloy Inorganic materials 0.000 title claims abstract description 80
- 239000003353 gold alloy Substances 0.000 title claims abstract description 46
- 238000004040 coloring Methods 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims abstract description 12
- 239000010931 gold Substances 0.000 claims abstract description 92
- 229910052737 gold Inorganic materials 0.000 claims abstract description 48
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims abstract description 45
- 238000002844 melting Methods 0.000 claims abstract description 43
- 230000008018 melting Effects 0.000 claims abstract description 43
- 238000010438 heat treatment Methods 0.000 claims abstract description 27
- 229910052802 copper Inorganic materials 0.000 claims abstract description 13
- 239000002344 surface layer Substances 0.000 claims abstract description 13
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000001301 oxygen Substances 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
- 230000001590 oxidative effect Effects 0.000 claims abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims abstract 5
- 239000010949 copper Substances 0.000 claims description 33
- 239000010936 titanium Substances 0.000 claims description 30
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 29
- 229910045601 alloy Inorganic materials 0.000 claims description 29
- 239000000956 alloy Substances 0.000 claims description 29
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 19
- 229910017052 cobalt Inorganic materials 0.000 claims description 12
- 239000010941 cobalt Substances 0.000 claims description 12
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 12
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 10
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 9
- 229910052709 silver Inorganic materials 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 239000003086 colorant Substances 0.000 claims description 6
- 239000004332 silver Substances 0.000 claims description 6
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 abstract description 44
- 238000005266 casting Methods 0.000 abstract description 30
- 229910052742 iron Inorganic materials 0.000 abstract description 5
- 238000009750 centrifugal casting Methods 0.000 abstract description 3
- 229910000510 noble metal Inorganic materials 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 54
- 238000002791 soaking Methods 0.000 description 8
- 239000002131 composite material Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000005498 polishing Methods 0.000 description 5
- 239000010970 precious metal Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 229910000881 Cu alloy Inorganic materials 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 229910017398 Au—Ni Inorganic materials 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910000925 Cd alloy Inorganic materials 0.000 description 1
- 229910002482 Cu–Ni Inorganic materials 0.000 description 1
- 229910000979 O alloy Inorganic materials 0.000 description 1
- 229910003087 TiOx Inorganic materials 0.000 description 1
- 241000665112 Zonitoides nitidus Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- HLLICFJUWSZHRJ-UHFFFAOYSA-N tioxidazole Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)SC2=C1 HLLICFJUWSZHRJ-UHFFFAOYSA-N 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A44—HABERDASHERY; JEWELLERY
- A44C—PERSONAL ADORNMENTS, e.g. JEWELLERY; COINS
- A44C27/00—Making jewellery or other personal adornments
- A44C27/001—Materials for manufacturing jewellery
- A44C27/002—Metallic materials
- A44C27/003—Metallic alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C5/00—Alloys based on noble metals
- C22C5/02—Alloys based on gold
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Adornments (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Contacts (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、貴金属装飾品製造に関連する光沢のある黒色
に着色する金合金とその着色法に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a gold alloy that is colored shiny black and a method for coloring the gold alloy, which is related to the production of precious metal ornaments.
(従来の技術〉
貴金属装飾品分野においては、金製品はカラブト法によ
り定められ、我が国では金含有量が75重量%の18力
ラツト加工品が流通している商品の90%以上を占めて
いる。これは、18カラツト金が機鍼的、物理的、化学
的性質が最も安定して加工性がよく、さらに色相の変化
等への応用がしやすいため定着したものと認められる。(Conventional technology) In the field of precious metal accessories, gold products are defined by the Karabut Law, and in Japan, 18-strength processed products with a gold content of 75% by weight account for more than 90% of the products in circulation. This is because 18 karat gold has become popular because it has the most stable mechanical, physical, and chemical properties, is easy to process, and is easy to apply to changes in hue.
そして、18カラツト金の色相は黄金色という概念が長
く固定化していたが、近年になって消費者の金合金によ
る貴金属装飾品のニーズが多様化し、多色化してデザイ
ンを生かす工夫がされるようになってきた。The concept that the hue of 18 karat gold is golden has long been fixed, but in recent years consumers' needs for precious metal ornaments made from gold alloys have diversified, and efforts have been made to utilize multi-colored designs. It's starting to look like this.
現在、金合金の製品に用いられている色相は、Au−へ
g合金の淡緑黄色、Au−^g−Cu合金の黄色、Au
−Cu合金の赤色、Au −Cu −Ni合金の淡黄白
色があり、これらの色を組み合せることによってカラフ
ルな加工品としていた。なお、極く最近になって、 A
u−^1金合金紫、Au−Cd合金の黄緑色が加わって
色彩に変化をもたらせることが可能となった。Currently, the hues used for gold alloy products are pale green-yellow for Au-heg alloy, yellow for Au-^g-Cu alloy, and yellow for Au-^g-Cu alloy.
-Cu alloy is red, and Au-Cu-Ni alloy is pale yellow-white, and by combining these colors, colorful processed products have been created. Furthermore, very recently, A.
It became possible to bring about a change in color by adding purple of the u-^1 gold alloy and yellow-green of the Au-Cd alloy.
〈発明が解決しようとする課題)
しかし、上記のように白、黄、赤、紫、黄緑の三色では
、装飾品としての多色デザイン化を図る上で限界があり
、上記以外の有色Au合金、特に消費量の多い黄金色に
対してコントラストが極めて良い黒色化した金合金の開
発が要望されているのが現状である。(Problem to be solved by the invention) However, as mentioned above, using the three colors of white, yellow, red, purple, and yellow-green has a limit in creating a multicolor design as an ornament. Currently, there is a demand for the development of a black gold alloy that has an extremely good contrast with the gold color of Au alloys, which is consumed in large quantities.
く課題を解決するための手段〉
本発明は上記に鑑み提案されたもので、純金(Au)に
、銅(Cu)、鉄(Fe)、コバルト(CO)もしくは
チタン(Titのうち1種が5〜65重量%含有する金
合金、
金(Au)の含有量が38重量%以上の金(Au)−銀
(八g)合金、もしくは金(Au)の含有量が38重量
%以上の金(Aul−ニッケル(Ni)合金に、銅(C
u) 、鉄(Fe) 、 コバルト(CO)もしくは
チタン(Ti、)のうち1種が5〜65重量%含有し、
金以外の元素の総量が65重量%を越えない金合金、
純金(Au)、もしくは金(Aulの含有量が38重量
%以上の金(Au)−銀(Ag1合金、もしくは金(A
ulの含有量が38重量%以上の金(Au)−ニッケル
(Ni)合金に55〜40重量%のIII (Cu)、
3〜40重量%の鉄(Fe)、 3〜40重量%のコ
バルト(Co) 。Means for Solving the Problems> The present invention was proposed in view of the above, and includes pure gold (Au) and one of copper (Cu), iron (Fe), cobalt (CO), or titanium (Tit). Gold alloy containing 5 to 65% by weight, gold (Au)-silver (8g) alloy containing 38% by weight or more of gold (Au), or gold containing 38% by weight or more of gold (Au) (Aul-nickel (Ni) alloy, copper (C)
u) Contains 5 to 65% by weight of one of iron (Fe), cobalt (CO), or titanium (Ti),
Gold alloy, pure gold (Au), or gold (gold (Au)-silver (Ag1 alloy) in which the total content of elements other than gold does not exceed 65% by weight, or gold (Au) with a content of 38% or more by weight)
Gold (Au)-nickel (Ni) alloy with an ul content of 38% by weight or more, 55 to 40% by weight of III (Cu),
3-40% by weight iron (Fe), 3-40% by weight cobalt (Co).
1〜10重量%のチタン(TL)もしくは0.5〜10
重量%の亜鉛(Zn)のうち2種以上を含有し、全以外
の元素の総量が5〜65重量%の金合金を、金合金の融
点以下の温度において大気中もしくは大気の酸素分圧よ
り高いかもしくは低い酸化雰囲気中で加熱処理を施した
後、空冷、水冷もしくは油冷して金合金の加工品の表層
部の全体もしくは一部を光沢のある黒色に着色する金合
金とその着色法に関するものである。1-10% by weight of titanium (TL) or 0.5-10
A gold alloy containing two or more types of zinc (Zn) with a total content of 5 to 65% by weight of all other elements is heated in the atmosphere or at the atmospheric oxygen partial pressure at a temperature below the melting point of the gold alloy. A gold alloy and its coloring method in which the whole or part of the surface layer of a processed gold alloy product is colored glossy black by heat treatment in a high or low oxidation atmosphere and then air-cooled, water-cooled, or oil-cooled. It is related to.
上記した各種の元素から構成される金合金は、上記した
各々の組成物を真空または、不活性ガス雰囲気中におい
て水冷銅ルツボを備久たアーク溶解炉或いは高周波溶解
炉等により溶製することにより得られる。Gold alloys composed of the various elements described above are produced by melting each of the above-mentioned compositions in a water-cooled copper crucible in a vacuum or in an inert gas atmosphere using a built-in arc melting furnace or high-frequency melting furnace. can get.
また、通常、−回の溶解量は50〜IQOgはどである
。Moreover, the amount of dissolution for - times is usually 50 to IQOg.
上記のように溶製した各合金のインゴットを真空もしく
は不活性ガス、例えばアルゴンガス雰囲気中において溶
解し、マグネシア、ジルコン、アルミナ、ムライト、シ
リカ等で作られた鋳型へ鋳造する。この場合、鋳造時に
不活性ガスによる加圧もしくは遠心力を利用して鋳型内
の空洞(キャビティ)への充填性を良好にすることが望
ましい。The ingots of each alloy produced as described above are melted in vacuum or in an inert gas atmosphere, such as argon gas, and cast into a mold made of magnesia, zircon, alumina, mullite, silica, or the like. In this case, it is desirable to use pressurization with an inert gas or centrifugal force during casting to improve filling of the cavity in the mold.
上記のように鋳造して得られた金合金の製品には、ヤス
リかけ、キサゲ、砥石研磨、パフ研磨を施した後、大気
中もしくは大気の酸素分圧より高いかまたは低い酸化雰
囲気中で、通常は850〜950℃で2〜3分はど加熱
した後、空冷、油冷もしくは水冷する。The gold alloy product obtained by casting as described above is subjected to sanding, scraping, whetstone polishing, and puff polishing, and then is heated in the atmosphere or in an oxidizing atmosphere higher or lower than the oxygen partial pressure of the atmosphere. Usually, it is heated at 850 to 950°C for 2 to 3 minutes, and then cooled in air, oil, or water.
上記した金合金の加熱工程は、大気中において行うもの
でもよく、また、加熱温度は各合金の融点以下の温度な
らば任意に2加熱時間についても任意に変えることがで
きる。The heating process for the gold alloy described above may be carried out in the atmosphere, and the heating temperature can be arbitrarily changed for two heating times as long as it is below the melting point of each alloy.
尚、上記した黒色化処理が終了した時点で1表面に形成
された黒色の光沢が不十分であれば、再度、軽(パフ研
磨を行った後、都市ガス、プロパンガス等によるガスバ
ーナーの炎を製品の表面に短時間あてて、パフ研磨によ
りつや出しすると十分な光沢を発生することができる。If the black gloss formed on the surface is insufficient after the above-mentioned blackening process is completed, perform light (puff polishing) again, and then burn the flame of a gas burner using city gas, propane gas, etc. A sufficient gloss can be generated by applying the product to the surface of the product for a short time and polishing it with a puff polish.
ところで、本発明の加熱1こよる黒色の発色処理は、加
工品の大きさにより異なるが、かなり広い範囲にとるこ
とが可能であり、加熱温度は大気雰囲気下では800〜
1000℃(らいで、加熱時間を長くするほど黒色化層
が厚くなるので、より黒色化度は増すが、指輪、ブロー
チ等の小物では2〜3分、少し大物でも3〜5分で十分
のようである。By the way, the black coloring process by heating 1 of the present invention varies depending on the size of the processed product, but it can be applied over a fairly wide range, and the heating temperature can be 800 - 800℃ in an atmospheric environment.
The longer the heating time, the thicker the blackening layer and therefore the degree of blackening. It seems so.
〈実施例)
最も一般的なAu品位の18カラツト(Au=75重量
%)の合金について実施した例を以下に示す。<Example> An example carried out using an alloy of 18 carats (Au = 75% by weight), which is the most common Au grade, is shown below.
(A)、純金にCu、 Fe、 Co、 Tiのうち1
種を添加した合金系の場合。(A) Pure gold with one of Cu, Fe, Co, and Ti
For alloy systems with added seeds.
実施例1
へ〇合金の配合
純^u 75g
電解Fe 25 g
上記配合のものをアルゴンガス雰囲気中において、アー
ク溶解により溶製した0本合金を真空下でロストワック
ス法により作製した鋳型を用い、遠心鋳造を行って得ら
れた鋳造品(指til)にヤスリがけ、研磨をして表面
を仕上げた後、大気中で900℃で2分間均熱して発色
処理した後、水冷した。その後、製品に再度パフ研磨を
施したところ、美麗で、光輝ある黒色製品が得られた0
発色処理により形成された黒色化層の厚さは、3〜4μ
mはどで、黒色化層を形成する組成物はAuを含むFe
5O4の酸化物であった。Example 1 〇 Alloy blend pure^u 75 g Electrolytic Fe 25 g The above-mentioned alloy was melted by arc melting in an argon gas atmosphere, using a mold made by the lost wax method under vacuum. The surface of the cast product (finger tiled) obtained by centrifugal casting was finished by filing and polishing, and then soaked in the air at 900° C. for 2 minutes to develop a color, and then cooled with water. After that, the product was puff-polished again, and a beautiful, shiny black product was obtained.
The thickness of the blackening layer formed by coloring treatment is 3 to 4 μm.
At m, the composition forming the blackening layer is Fe containing Au.
It was an oxide of 5O4.
実施例2
Au合金の配合
純Au 75 g
純Ti 25 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(詣輸)を大気中で850℃で2分間均熱した後、空
冷して、製品の表層郡全体を黒色化させた。黒色層は2
〜3μmはどで、黒色化層の組成物はAuを含むT +
、 Ozの低次酸化物であった。Example 2 Au alloy composition Pure Au 75 g Pure Ti 25 g The cast product (transportation) obtained by melting and casting in the same manner as in Example 1 was soaked in the atmosphere at 850°C for 2 minutes. After that, the product was air cooled to blacken the entire surface layer of the product. The black layer is 2
~3 μm, the composition of the blackening layer is T + containing Au
, Oz was a lower oxide.
実施例3
Au合金の配合
純Au 75 g
電解Co 25 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で950℃で3分間均熱した後、空
冷して、製品の浅層部全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物はAuを含むCoOで
あった。Example 3 Blend of Au alloy Pure Au 75 g Electrolytic Co 25 g The cast product (ring) obtained by melting and casting in the same manner as in Example 1 was soaked at 950°C for 3 minutes in the air. After that, the product was air cooled to blacken the entire shallow layer of the product. The black layer is 3
~4 μm, and the composition of the black layer was CoO containing Au.
実施例4
Au合金の配合
純^u 75g
無酸素Cu 25 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で800℃で2分間均熱した後、空
冷して、製品の浅層部全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物はAuを含むCuOで
あ7た。Example 4 Mixture of Au alloy Pure^u 75g Oxygen-free Cu 25g The cast product (ring) obtained by melting and casting in the same manner as in Example 1 was soaked in the atmosphere at 800°C for 2 minutes. After that, the product was air cooled to blacken the entire shallow layer of the product. The black layer is 3
The thickness was ~4 μm, and the composition of the black layer was CuO containing Au.
(B)、Au−Ag合金(Au含有量38重量%以上)
もしくはAu−Ni合金(Au含有量38重量%以上)
にCu、 Fe、 Go、 Tiのうち1種を添加した
合金系の場合。(B), Au-Ag alloy (Au content 38% by weight or more)
Or Au-Ni alloy (Au content 38% by weight or more)
In the case of an alloy system in which one of Cu, Fe, Go, and Ti is added.
実施例5
Au合金の配合
純Au 75 g
純AI! 10g
電解Fe l 5 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中でsoo℃で2分間均熱した後、空
冷して、製品の浅層部全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物の多(はAu、Agを
含むFe5OaであったがAg!。Example 5 Au alloy composition Pure Au 75 g Pure AI! 10 g Electrolytic Fe l 5 g The cast product (ring) obtained by melting and casting in the same manner as in Example 1 was soaked in the air at soo Celsius for 2 minutes, then air cooled, and the product was shallowly heated. The entire layer was blackened. The black layer is 3
~4 μm, and the composition of the black layer was Fe5Oa containing Au and Ag, but Ag!
がわずかに含まれていた。contained a small amount.
実施例6
Au合金の配合
純Au 75 g
純Ag l Og
電解Go 15 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で1150’cで3分間均熱した後
、空冷して、製品の浅層部全体を黒色化させた。黒色層
は2〜3μmはどで、黒色層の組成物の多くはAu、
Agを含むCooであったが八g、oがわずかに含まれ
ていた。Example 6 Au alloy composition Pure Au 75 g Pure Ag l Og Electrolytic Go 15 g A cast product (ring) obtained by melting and casting in the same manner as in Example 1 was heated at 1150'c in the atmosphere. After soaking for 3 minutes, the product was air cooled to blacken the entire shallow layer of the product. The black layer has a thickness of 2 to 3 μm, and most of the composition of the black layer is Au,
Although Coo contained Ag, it contained a small amount of 8g and o.
実施例7
Au合金の配合
純Au 75 g
純Ag 17g
純Ti 8g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で850℃で3分間均熱した後、空
冷して、製品の浅層部全体を黒色化させた。黒色層は2
〜3μmはどで、黒色層の組成物はAu、 Agを含む
TiOxの低次酸化物であった。Example 7 Combination of Au alloy Pure Au 75 g Pure Ag 17 g Pure Ti 8 g The cast product (ring) obtained by melting and casting in the same manner as in Example 1 was equalized in the air at 850°C for 3 minutes. After heating, the product was air cooled to blacken the entire shallow layer of the product. The black layer is 2
The thickness was ~3 μm, and the composition of the black layer was a low-order oxide of TiOx containing Au and Ag.
実施例8
Au合金の配合
純Au 75 g
電解Ni 10 g
無fII素Cu 15g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で800℃で2分間均熱した後、空
冷して、製品の浅層部全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物はAu、 NiOを含
むCuOであった。Example 8 Blend of Au alloy Pure Au 75 g Electrolytic Ni 10 g FII-free Cu 15 g A cast product (ring) obtained by melting and casting in the same manner as in Example 1 was heated at 800°C in the atmosphere. After soaking for 2 minutes, the product was air cooled to blacken the entire shallow layer of the product. The black layer is 3
~4 μm, and the composition of the black layer was CuO containing Au and NiO.
実施例9
Au合金の配合
純^u 75g
電解Ni 15g
電解Fs 10 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で850℃で2分間均熱した後、空
冷して、製品の浅層部全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物の多くはAu、 Ni
を含むFe50*であった。Example 9 Mixture of Au alloy Purity^u 75g Electrolytic Ni 15g Electrolytic Fs 10g A cast product (ring) obtained by melting and casting in the same manner as in Example 1 was heated at 850°C for 2 minutes in the atmosphere. After soaking, the product was air cooled to blacken the entire shallow layer of the product. The black layer is 3
~ 4 μm, and most of the composition of the black layer is Au, Ni
It was Fe50* containing.
(C)、純金、もしくは^U−八gへ金(Au含有量3
8重量%以上)、もしくはAu−Ni合金(Au含有量
38重量%以上)にCu、 Fe、 Go、 Ti、Z
nのうち2種以上を添加した合金系の場合。(C), pure gold or ^U-8g gold (Au content 3
8% by weight or more) or Au-Ni alloy (Au content 38% by weight or more) with Cu, Fe, Go, Ti, Z
In the case of an alloy system in which two or more types of n are added.
実施例10
Au合金の配合
純^u 75g
電解Go 18 g
電解Fe 7g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で900℃で2分間均熱した後、空
冷して、製品の表層郡全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物はAuを含むFflt
OnとCoOの複合酸化物であった。Example 10 Mixture of Au alloy Purity^u 75g Electrolytic Go 18g Electrolytic Fe 7g A cast product (ring) obtained by melting and casting in the same manner as Example 1 was heated at 900°C for 2 minutes in the atmosphere. After soaking, the product was air cooled to blacken the entire surface layer of the product. The black layer is 3
~4μm, the composition of the black layer is Fflt containing Au
It was a composite oxide of On and CoO.
実施例11
Au合金の配合
純Au 75 g
電解Co 20 g
純Ti 5g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で90O℃で3分間均熱した後、空
冷して、製品の表り部全体を黒色化させた。黒色層は2
〜3μmはどで、黒色層の組成物はAuを含むCooと
Ti0mの低次酸化物との複合酸化物であった。Example 11 Mixture of Au alloy Pure Au 75 g Electrolytic Co 20 g Pure Ti 5 g The cast product (ring) obtained by melting and casting in the same manner as in Example 1 was heated at 900°C for 3 minutes in the atmosphere. After soaking, the product was air-cooled to turn the entire surface of the product black. The black layer is 2
The thickness was ~3 μm, and the composition of the black layer was a composite oxide of Coo containing Au and a lower oxide of Ti0m.
実施例12
Au合金の配合
純Au 75 g
電解Co 20 g
無酸素Cu 5g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で800℃で2分間均熱した後、空
冷して、製品の表層郡全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物はAuを含むCoOと
CuOの複合酸化物であった。Example 12 Blend of Au alloy Pure Au 75 g Electrolytic Co 20 g Oxygen-free Cu 5 g A cast product (ring) obtained by melting and casting in the same manner as in Example 1 was heated at 800°C in the atmosphere for 2 hours. After soaking for a minute, the product was air cooled to blacken the entire surface layer of the product. The black layer is 3
The thickness was ~4 μm, and the composition of the black layer was a composite oxide of CoO and CuO containing Au.
実施例13
Au合金の配合
純^u 75g
電解Fe 24g
純Zn 1 g
実施例1と同一の方法で溶製し、鋳造して得られた鋳造
品(指輪)を大気中で800℃で2分間均熱した後、空
冷して、製品の表層郡全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物は^Uを含むFe5O
4に極く僅少量のZnOが含まれていた。Example 13 Mixture of Au alloy Pure^u 75g Electrolytic Fe 24g Pure Zn 1g A cast product (ring) obtained by melting and casting in the same manner as Example 1 was heated at 800°C for 2 minutes in the atmosphere. After soaking, the product was air cooled to blacken the entire surface layer of the product. The black layer is 3
~4 μm, the composition of the black layer is Fe5O containing ^U
4 contained a very small amount of ZnO.
実施例14
Au合金の配合
純^u 75g
電解Fe 10 g
無酸素Cu 15 g
実施例1と同一の方法で浩製し、鋳造して得られた鋳造
品(指輪)を大気中で850℃で2分間均熱した後、空
冷して、製品の表層郡全体を黒色化させた。黒色層は3
〜4μmはどで、黒色層の組成物はAuを含むFe5O
aとCuOの複合酸化物であった。Example 14 Mixture of Au alloy Pure^u 75 g Electrolytic Fe 10 g Oxygen-free Cu 15 g A cast product (ring) was produced and cast in the same manner as in Example 1 at 850°C in the atmosphere. After soaking for 2 minutes, the product was air cooled to blacken the entire surface layer of the product. The black layer is 3
~4 μm, and the composition of the black layer is Fe5O containing Au.
It was a composite oxide of a and CuO.
実施例15
Au合金の配合
純Au 75g
電解Co 10 g
電解Fe l 3 g
純11 2g
実施例1と同様の溶製方法によりAu−Go−Fe−T
i合金を得た。その後、この合金を用いて遠心鋳造を行
って得られた鋳造品(指輪)に大気中で900℃で3分
の余熱処理を行なって黒色に発色させ、水冷した。黒色
化層の厚さは3〜4Iimはどで、美麗であった。Example 15 Combination of Au alloy Pure Au 75 g Electrolytic Co 10 g Electrolytic Fe 3 g Pure 11 2 g Au-Go-Fe-T was prepared by the same melting method as in Example 1.
i alloy was obtained. Thereafter, a cast product (ring) obtained by performing centrifugal casting using this alloy was preheated in the atmosphere at 900° C. for 3 minutes to develop a black color, and then cooled in water. The thickness of the blackened layer was 3 to 4 Im and was beautiful.
実施例16
Au合金の配合
純^u 75g
純へg log
電解Co 5g
電解Fe 9g
純Tt 1 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った。黒色化層の厚さは3〜4μmはどで、黒色化層は
、Auを含むAg、 Co、 Fe、 Tiの複合酸化
物であった。Example 16 Mixture of Au alloy Pure^u 75g Pure Heg log Electrolytic Co 5g Electrolytic Fe 9g Pure Tt 1g The same coloring treatment as in Example 1 was performed by melting, casting, and heating. The thickness of the blackening layer was 3 to 4 μm, and the blackening layer was a composite oxide of Ag, Co, Fe, and Ti containing Au.
実施例17
Au合金の配合
純^u 75g
純へg 10[
無酸素Cu 5g
電解Co 10 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 17 Mixture of Au alloy Pure^u 75g Pureheg 10 [Oxygen-free Cu 5g Electrolytic Co 10g The same coloring treatment as in Example 1 was performed by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. And it was beautiful.
実施例18
Au合金の配合
純Au 75 g
純へg 10g
無酸素Cu 5g
電解Fe 10 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った。黒色化層は3〜4μmであり、美麗であった。Example 18 Composition of Au alloy Pure Au 75 g Pure Au 10 g Oxygen-free Cu 5 g Electrolytic Fe 10 g The same coloring treatment as in Example 1 was performed by melting, casting, and heating. The blackened layer had a thickness of 3 to 4 μm and was beautiful.
実施例19
Au合金の配合
純^u 75g
純Ag 10 g
無酸素Cu 10 g
純Ti 5g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 19 Mixture of Au alloy Pure^u 75g Pure Ag 10g Oxygen-free Cu 10g Pure Ti 5g The same coloring treatment as in Example 1 was performed by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. Yes, it was beautiful.
実施例20
Au合金の配合
純Au 75 g
純Ag 10g
無酸素Cu 5g
電解Co 5g
電解Fe 5g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 20 Combination of Au alloy Pure Au 75 g Pure Ag 10 g Oxygen-free Cu 5 g Electrolytic Co 5 g Electrolytic Fe 5 g The same coloring treatment as in Example 1 was performed by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. And it was beautiful.
実施例21
Au合金の配合
純Au 75 g
純へg 10g
無酸素Cu 5g
電解Go 8g
純Ti 2g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 21 Mixture of Au alloy Pure Au 75 g Pure Au 10 g Oxygen-free Cu 5 g Electrolytic Go 8 g Pure Ti 2 g The same coloring treatment as in Example 1 was carried out by melting, casting, and heating, and the blackening layer was 3~ It was 4 μm and beautiful.
実施例22
Au合金の配合
純^u 75g
純Ag log
無酸素Cu 5g
電解Fe 8g
純Ti 2g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 22 Mixture of Au alloy Purity^u 75g Pure Ag log Oxygen-free Cu 5g Electrolytic Fe 8g Pure Ti 2g The same coloring treatment as in Example 1 was performed by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. And it was beautiful.
実施例23
Au合金の配合
純Au 75 g
無酸素Cu 5g
電解Go 10 g
電解Fe 10 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 23 Composition of Au alloy Pure Au 75 g Oxygen-free Cu 5 g Electrolytic Go 10 g Electrolytic Fe 10 g The same coloring treatment as in Example 1 was carried out by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. Yes, it was beautiful.
実施例24
Au合金の配合
純Au 75 g
無酸素Cu 3g
電解Co 20 g
純Ti 2g実施例1と同様
の溶製、鋳造、加熱による発色処理を行った、黒色化層
は3〜4μmであり、美麗であった。Example 24 Combination of Au alloy Pure Au 75 g Oxygen-free Cu 3 g Electrolytic Co 20 g Pure Ti 2 g The same coloring treatment as in Example 1 was carried out by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. , it was beautiful.
実施例25
Au合金の配合
純^u 75g
無酸素Cu 2g
電解Go 15g
電解Fe 7 g
純Ti l g
実施例1と同様の溶製、uI造、加熱による発色処理を
行った、黒色化層は3〜4μmであり、美麗であった。Example 25 Mixture of Au alloy Pure^u 75g Oxygen-free Cu 2g Electrolytic Go 15g Electrolytic Fe 7g Pure Ti lg The blackening layer was subjected to the same coloring treatment as in Example 1 by melting, ul-forming, and heating. It was 3 to 4 μm and beautiful.
実施例26
Au合金の配合
純Au 75 g
純Ag 10 g
電解Ni 5g
電解Go 10 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った。黒色化層は3〜4μmであり、美麗であった。Example 26 Composition of Au alloy Pure Au 75 g Pure Ag 10 g Electrolytic Ni 5 g Electrolytic Go 10 g The same coloring treatment as in Example 1 was performed by melting, casting, and heating. The blackened layer had a thickness of 3 to 4 μm and was beautiful.
実施例27
Au合金の配合
純^u 75に
純へg Log
電解Ni 5g
電解Fe 9g
純Ti 1 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った。黒色化層は3〜4μmであり、美麗であった。Example 27 Mixture of Au alloy Pure^u 75 to pure g Log Electrolytic Ni 5g Electrolytic Fe 9g Pure Ti 1g The same coloring treatment as in Example 1 was performed by melting, casting, and heating. The blackened layer had a thickness of 3 to 4 μm and was beautiful.
実施例28
Au合金の配合
純^u 75g
純Ag 15 g
電解Ml 5g
純Ti 5g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 28 Mixture of Au alloy Pure^u 75g Pure Ag 15g Electrolytic Ml 5g Pure Ti 5g The same coloring treatment as in Example 1 was performed by melting, casting, and heating, and the blackening layer was 3 to 4 μm thick. It was beautiful.
実施例29
Au合金の配合
純Au 75 g
純へg log
電解Nl 2g
電解Co 6g
電解Fe 6g
純Zn 1 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 29 Mixture of Au alloy Pure Au 75 g Pure heg log Electrolytic Nl 2 g Electrolytic Co 6 g Electrolytic Fe 6 g Pure Zn 1 g Blackened layer subjected to coloring treatment by melting, casting, and heating in the same manner as in Example 1 It was 3 to 4 μm and beautiful.
実施例30
Au合金の配合
純^、 75g
純へg 10g
電解Ni 3g
電解Co 10 g
純Ti l g
純Zn 1 g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 30 Mixture of Au alloy Pure ^, 75 g Pure Heg 10 g Electrolytic Ni 3 g Electrolytic Co 10 g Pure Ti l g Pure Zn 1 g Black color obtained by coloring treatment by melting, casting, and heating in the same manner as in Example 1 The layer was 3 to 4 μm thick and beautiful.
実施例31
^1金合金配合
純Au
純Ag
電解Ni
電解Fe
電解CO
純Ti
純Zn
5g
5g
3g
3g
3g
3g
3g
実施例1と同様の溶製、鋳造、加熱による発色処理を行
った、黒色化層は3〜4μmであり、美麗であった。Example 31 ^1 Gold alloy blend Pure Au Pure Ag Electrolytic Ni Electrolytic Fe Electrolytic CO Pure Ti Pure Zn 5g 5g 3g 3g 3g 3g 3g Blackened by coloring treatment by melting, casting, and heating similar to Example 1 The layer was 3-4 μm thick and beautiful.
以上、18K (カラット)のAu合金についての実施
例を記したが、IgK以上の例えば20K、22に等及
びL8に以下のAu合金においても、前記した本発明の
構成に示した範囲において添加元素と添加量の調整をし
たAu合金の貴金属製品に対し、加熱処理を施すことに
より黒色化した製品とすることができる。Above, examples have been described for Au alloys of 18K (carats), but in Au alloys of IgK or higher, such as 20K, 22, etc., and L8 or less, additive elements can be added within the range shown in the constitution of the present invention described above. A blackened product can be obtained by heat-treating a precious metal product made of an Au alloy with an adjusted amount of addition.
(発明の効果〉
以上説明したように、本発明の金合金は、従来、赤、黄
、黄緑、白、紫の5色であったAu合金に、黒色を加え
ることになり、貴金属装飾品としてより多彩なデザイン
が可能になるとともに、装飾品の高付加価値化につなが
る。(Effects of the Invention) As explained above, the gold alloy of the present invention adds black to the conventional Au alloy, which has five colors of red, yellow, yellow-green, white, and purple, and can be used for precious metal ornaments. This not only makes it possible to create a wider variety of designs, but also leads to higher added value for decorative items.
また、本発明の光沢のある黒色に着色する金合金の製造
法は、特殊な原材料及び処理装置を必要としないので、
適用性は極めて高い。In addition, the method for producing a gold alloy that is colored shiny black according to the present invention does not require special raw materials or processing equipment.
The applicability is extremely high.
手続補正書(1劃 平成2年4月27日Procedural amendment (part 1) April 27, 1990
Claims (6)
ルト(Co)もしくはチタン(Ti)のうち1種が5〜
65重量%含有する金合金を、金合金の融点以下の温度
において大気中もしくは大気の酸素分圧より高いかもし
くは低い酸化雰囲気中で加熱処理を施した後、空冷、水
冷もしくは油冷し、金合金の加工品の表層部の全体もし
くは一部を光沢のある黒色に着色する金合金。(1) One of copper (Cu), iron (Fe), cobalt (Co), or titanium (Ti) is added to pure gold (Au) from 5 to 50%.
A gold alloy containing 65% by weight is heat treated in the atmosphere or in an oxidizing atmosphere higher or lower than the oxygen partial pressure of the atmosphere at a temperature below the melting point of the gold alloy, and then air-cooled, water-cooled, or oil-cooled to form a gold alloy. A gold alloy that colors the entire or part of the surface layer of processed alloy products a glossy black color.
ルト(Co)もしくはチタン(Ti)のうち1種が5〜
65重量%含有する金合金を、金合金の融点以下の温度
において大気中もしくは大気の酸素分圧より高いかもし
くは低い酸化雰囲気中で加熱処理を施した後、空冷、水
冷もしくは油冷して金合金の加工品の表層部の全体もし
くは一部を光沢のある黒色に着色する金合金の着色法。(2) One of copper (Cu), iron (Fe), cobalt (Co), or titanium (Ti) is added to pure gold (Au) from 5 to 50%.
A gold alloy containing 65% by weight is heat treated in the atmosphere or in an oxidizing atmosphere higher or lower than the oxygen partial pressure of the atmosphere at a temperature below the melting point of the gold alloy, and then air-cooled, water-cooled, or oil-cooled to produce gold. A gold alloy coloring method that colors all or part of the surface layer of a processed alloy product a glossy black color.
)−銀(Ag)合金、もしくは金(Au)の含有量が3
8重量%以上の金(Au)−ニッケル(Ni)合金に、
銅(Cu)、鉄(Fe)、コバルト(Co)もしくはチ
タン(Ti)のうち1種が5〜65重量%含有し、金以
外の元素の総量が65重量%を越えない金合金を、金合
金の融点以下の温度において大気中もしくは大気の酸素
分圧より高いかもしくは低い酸化雰囲気中で加熱処理を
施した後、空冷、水冷もしくは油冷し、金合金の加工品
の表層部の全体もしくは一部を光沢のある黒色に着色す
る金合金。(3) Gold (Au) with a gold (Au) content of 38% by weight or more
) - Silver (Ag) alloy or gold (Au) content of 3
8% by weight or more of gold (Au)-nickel (Ni) alloy,
A gold alloy containing 5 to 65% by weight of one of copper (Cu), iron (Fe), cobalt (Co), or titanium (Ti), and in which the total amount of elements other than gold does not exceed 65% by weight, is After heat treatment in the atmosphere or in an oxidizing atmosphere higher or lower than the atmospheric oxygen partial pressure at a temperature below the melting point of the alloy, the entire surface layer of the gold alloy processed product or A gold alloy that is partially colored a glossy black color.
)−銀(Ag)合金、もしくは金(Au)の含有量が3
8重量%以上の金(Au)−ニッケル(Ni)合金に、
銅(Cu)、鉄(Fe)、コバルト(Co)もしくはチ
タン(Ti)のうち1種が5〜65重量%含有し、金以
外の元素の総量が65重量%を越えない金合金を、金合
金の融点以下の温度において大気中もしくは大気の酸素
分圧より高いかもしくは低い酸化雰囲気中で加熱処理を
施した後、空冷、水冷もしくは油冷して金合金の加工品
の表層部の全体もしくは一部を光沢のある黒色に着色す
る金合金の着色法。(4) Gold (Au) with a gold (Au) content of 38% by weight or more
) - Silver (Ag) alloy or gold (Au) content of 3
8% by weight or more of gold (Au)-nickel (Ni) alloy,
A gold alloy containing 5 to 65% by weight of one of copper (Cu), iron (Fe), cobalt (Co), or titanium (Ti), and in which the total amount of elements other than gold does not exceed 65% by weight, is After heat treatment in the atmosphere or in an oxidizing atmosphere higher or lower than the oxygen partial pressure of the atmosphere at a temperature below the melting point of the alloy, the whole or surface layer of the gold alloy processed product is cooled by air, water or oil cooling. A method of coloring gold alloys that partially colors them a glossy black color.
8重量%以上の金(Au)−銀(Ag)合金、もしくは
金(Au)の含有量が38重量%以上の金(Au)−ニ
ッケル(Ni)合金に、5〜40重量%の銅(Cu)、
3〜40重量%の鉄(Fe)、3〜40重量%のコバル
ト(Co)、1〜10重量%のチタン(Ti)もしくは
0.5〜10重量%の亜鉛(Zn)のうち2種以上を含
有し、金以外の元素の総量が5〜65重量%の金合金を
、金合金の融点以下の温度において大気中もしくは大気
の酸素分圧より高いかもしくは低い酸化雰囲気中で加熱
処理を施した後、空冷、水冷もしくは油冷し、金合金の
加工品の表層部の全体もしくは一部を光沢のある黒色に
着色する金合金。(5) Pure gold (Au) or gold (Au) content of 3
A gold (Au)-silver (Ag) alloy containing 8% by weight or more, or a gold (Au)-nickel (Ni) alloy containing 38% by weight or more of gold (Au), and 5 to 40% by weight copper ( Cu),
Two or more of 3-40% by weight of iron (Fe), 3-40% by weight of cobalt (Co), 1-10% by weight of titanium (Ti), or 0.5-10% by weight of zinc (Zn) A gold alloy containing 5 to 65% by weight of elements other than gold is heat-treated in the atmosphere or in an oxidizing atmosphere higher or lower than the oxygen partial pressure of the atmosphere at a temperature below the melting point of the gold alloy. After that, the gold alloy is air-cooled, water-cooled, or oil-cooled to color the whole or part of the surface layer of the gold alloy processed product a glossy black color.
8重量%以上の金(Au)−銀(Ag)合金、もしくは
金(Au)の含有量が38重量%以上の金(Au)−ニ
ッケル(Ni)合金に、5〜40重量%の銅(Cu)、
3〜40重量%の鉄(Fe)、3〜40重量%のコバル
ト(Co)、1〜10重量%のチタン(Ti)もしくは
0.5〜10重量%の亜鉛(Zn)のうち2種以上を含
有し、金以外の元素の総量が5〜65重量%の金合金を
、金合金の融点以下の温度において大気中もしくは大気
の酸素分圧より高いかもしくは低い酸化雰囲気中で加熱
処理を施した後、空冷、水冷もしくは油冷して金合金の
加工品の表層部の全体もしくは一部を光沢のある黒色に
着色する金合金の着色法。(6) Pure gold (Au) or gold (Au) content of 3
A gold (Au)-silver (Ag) alloy containing 8% by weight or more, or a gold (Au)-nickel (Ni) alloy containing 38% by weight or more of gold (Au), and 5 to 40% by weight copper ( Cu),
Two or more of 3-40% by weight of iron (Fe), 3-40% by weight of cobalt (Co), 1-10% by weight of titanium (Ti), or 0.5-10% by weight of zinc (Zn) A gold alloy containing 5 to 65% by weight of elements other than gold is heat-treated in the atmosphere or in an oxidizing atmosphere higher or lower than the oxygen partial pressure of the atmosphere at a temperature below the melting point of the gold alloy. A gold alloy coloring method in which the gold alloy is then air-cooled, water-cooled, or oil-cooled to color all or part of the surface layer of the processed gold alloy product a glossy black color.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1045420A JPH02225655A (en) | 1989-02-28 | 1989-02-28 | Gold alloy that is colored shiny black and its coloring method |
| CH4326/89A CH680735A5 (en) | 1989-02-28 | 1989-12-04 | |
| IT67023A IT1240937B (en) | 1989-02-28 | 1990-01-12 | GOLD ALLOY FOR COLORING IN BLACK, ARTICLE WORKED IN GOLD ALLOY COLORED IN BLACK AND METHOD FOR THE PRODUCTION OF THE ARTICLE WORKED |
| FR9000981A FR2643649B1 (en) | 1989-02-28 | 1990-01-29 | GOLD ALLOY FOR BLACK COLORING, TREATED BLACK COLORED GOLD ALLOY ARTICLE AND PROCESS FOR PRODUCING THE TREATED ARTICLE |
| DE4020329A DE4020329A1 (en) | 1989-02-28 | 1990-06-26 | GOLD ALLOY FOR BLACK COLORING, TREATED OR WORKED ARTICLES MADE OF BLACK-DYED GOLD ALLOY AND METHOD FOR THE PRODUCTION OF THE TREATED OR. EDITED ITEM |
| GB9014240A GB2245590A (en) | 1989-02-28 | 1990-06-26 | Gold alloy for black coloring, processed article of black colored gold alloy and method for production of the processed article |
| US07/682,898 US5139739A (en) | 1989-02-28 | 1991-04-09 | Gold alloy for black coloring, processed article of black colored gold alloy and method for production of the processed article |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1045420A JPH02225655A (en) | 1989-02-28 | 1989-02-28 | Gold alloy that is colored shiny black and its coloring method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02225655A true JPH02225655A (en) | 1990-09-07 |
Family
ID=12718777
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1045420A Pending JPH02225655A (en) | 1989-02-28 | 1989-02-28 | Gold alloy that is colored shiny black and its coloring method |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JPH02225655A (en) |
| CH (1) | CH680735A5 (en) |
| DE (1) | DE4020329A1 (en) |
| FR (1) | FR2643649B1 (en) |
| GB (1) | GB2245590A (en) |
| IT (1) | IT1240937B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04183836A (en) * | 1990-11-19 | 1992-06-30 | Seiko Instr Inc | Surface hardened colored gold alloy |
| JPH0657356A (en) * | 1991-11-14 | 1994-03-01 | Nippon Kogyo Ginkou:Kk | Gold alloy for decoration |
| JP2017518442A (en) * | 2014-12-29 | 2017-07-06 | モントレー ブレゲ・エス アー | Gold and titanium light noble metal alloys, and timer or jewelry parts made of such gold and titanium light noble metal alloys |
| CN112251625A (en) * | 2020-10-15 | 2021-01-22 | 深圳市宝瑞莱珠宝首饰有限公司 | Fading-resistant 18K black gold for jewelry and processing technology thereof |
| IT202200010889A1 (en) * | 2022-05-25 | 2023-11-25 | Patros S R L | Method for obtaining an object comprising titanium for jewellery, goldsmithing or costume jewelery and object thus obtained. |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02197539A (en) * | 1989-01-26 | 1990-08-06 | Tanaka Kikinzoku Kogyo Kk | Co-containing noble metallic material for ornaments |
| US5853661A (en) * | 1994-07-05 | 1998-12-29 | Cendres Et Metaux Sa | High gold content bio--compatible dental alloy |
| IT1280528B1 (en) * | 1995-06-27 | 1998-01-22 | Silmar Spa | GOLD-BASED ALLOYS |
| WO2006111178A1 (en) * | 2005-04-19 | 2006-10-26 | Ludwig Müller S.A. | Precious metal alloy |
| CH697875B1 (en) * | 2005-07-16 | 2009-03-13 | Ludwig Mueller | precious metal alloy. |
| SG160266A1 (en) * | 2008-09-08 | 2010-04-29 | Autium Pte Ltd | Coloured gold alloy and method for forming the same |
| RU2625199C1 (en) * | 2016-07-11 | 2017-07-12 | Юлия Алексеевна Щепочкина | Gold-based alloy |
| EP3553192B1 (en) * | 2018-04-12 | 2021-07-14 | Argor-Heraeus S.A. | Tarnishing resistant gold alloy at 14k and method of production thereof |
| IT201800004444A1 (en) * | 2018-04-12 | 2019-10-12 | 14K GOLD ALLOY RESISTANT TO TARNISHING AND PRODUCTION METHOD OF THE SAME | |
| EP4249149A1 (en) | 2022-03-24 | 2023-09-27 | Richemont International S.A. | Composite gold material for dark colouring and method for manufacturing same |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5288236A (en) * | 1976-01-19 | 1977-07-23 | Seiko Instr & Electronics | Ornamental coloring process |
| JPS6067694A (en) * | 1983-09-20 | 1985-04-18 | Katsusato Fujiyoshi | Color forming method of sintered noble metal |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH207103A (en) * | 1937-04-23 | 1939-09-30 | Heraeus Gmbh W C | Gold alloy, in particular for jewelry and rings. |
| US2141157A (en) * | 1938-08-23 | 1938-12-20 | Metals & Controls Corp | Alloy |
| US2164938A (en) * | 1938-08-23 | 1939-07-04 | Metals & Controls Corp | Alloy |
| US2229463A (en) * | 1939-10-21 | 1941-01-21 | Handy & Harman | Alloy |
| DE752627C (en) * | 1942-10-24 | 1951-08-06 | Degussa | Payable gold-platinum alloy |
| DE1121339B (en) * | 1957-07-12 | 1962-01-04 | Degussa | Deformable gold alloys for electrical conductors with high specific resistance |
| US3189482A (en) * | 1961-03-09 | 1965-06-15 | Gen Mills Inc | Metal film resistor and method of its formation |
| US3769006A (en) * | 1972-01-27 | 1973-10-30 | Gold Refining W Co | Bright cast alloy, and composition |
| US4012228A (en) * | 1976-05-14 | 1977-03-15 | Howmedica, Inc. | Low intrinsic value alloys |
| AU523626B2 (en) * | 1979-01-18 | 1982-08-05 | Murao Shoten K.K. | (au + cu) base-ag-zn alloy |
| GB2066291B (en) * | 1979-12-14 | 1984-01-25 | Atomic Energy Authority Uk | Ternary alloys |
| JPS575833A (en) * | 1980-06-11 | 1982-01-12 | Ishifuku Kinzoku Kogyo Kk | Gold permanent magnet alloy |
| JPS57120644A (en) * | 1981-01-16 | 1982-07-27 | Citizen Watch Co Ltd | Gold alloy with pinkish color tone |
| DE3142541C2 (en) * | 1981-10-27 | 1986-07-31 | Demetron Gesellschaft für Elektronik-Werkstoffe mbH, 6540 Hanau | Multi-component alloy for targets in cathode sputtering systems |
| JPS5923835A (en) * | 1982-07-28 | 1984-02-07 | Toyota Central Res & Dev Lab Inc | Method for manufacturing boride dispersed alloy |
| GB2138027B (en) * | 1983-04-12 | 1986-09-10 | Citizen Watch Co Ltd | A process for plating an article with a gold-based alloy and an alloy therefor |
| DE3406711C1 (en) * | 1984-02-24 | 1985-04-25 | Degussa Ag, 6000 Frankfurt | Low gold dental alloys |
| DE3502460A1 (en) * | 1985-01-25 | 1986-07-31 | C. Hafner GmbH + Co., 7530 Pforzheim | Process for generating dark surfaces on gold alloys |
| DE3502914A1 (en) * | 1985-01-29 | 1986-07-31 | International Gold Corp. Ltd., Johannesburg | USE OF TITANIUM GOLD ALLOYS |
| GB2184457B (en) * | 1985-12-06 | 1989-03-30 | Vittorio Antoniazzi | Gold alloy |
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| DE3835593C1 (en) * | 1988-10-19 | 1989-11-16 | Degussa Ag, 6000 Frankfurt, De |
-
1989
- 1989-02-28 JP JP1045420A patent/JPH02225655A/en active Pending
- 1989-12-04 CH CH4326/89A patent/CH680735A5/de not_active IP Right Cessation
-
1990
- 1990-01-12 IT IT67023A patent/IT1240937B/en active IP Right Grant
- 1990-01-29 FR FR9000981A patent/FR2643649B1/en not_active Expired - Fee Related
- 1990-06-26 DE DE4020329A patent/DE4020329A1/en not_active Ceased
- 1990-06-26 GB GB9014240A patent/GB2245590A/en not_active Withdrawn
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5288236A (en) * | 1976-01-19 | 1977-07-23 | Seiko Instr & Electronics | Ornamental coloring process |
| JPS6067694A (en) * | 1983-09-20 | 1985-04-18 | Katsusato Fujiyoshi | Color forming method of sintered noble metal |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04183836A (en) * | 1990-11-19 | 1992-06-30 | Seiko Instr Inc | Surface hardened colored gold alloy |
| JPH0657356A (en) * | 1991-11-14 | 1994-03-01 | Nippon Kogyo Ginkou:Kk | Gold alloy for decoration |
| JP2017518442A (en) * | 2014-12-29 | 2017-07-06 | モントレー ブレゲ・エス アー | Gold and titanium light noble metal alloys, and timer or jewelry parts made of such gold and titanium light noble metal alloys |
| CN112251625A (en) * | 2020-10-15 | 2021-01-22 | 深圳市宝瑞莱珠宝首饰有限公司 | Fading-resistant 18K black gold for jewelry and processing technology thereof |
| CN112251625B (en) * | 2020-10-15 | 2022-04-15 | 深圳市宝瑞莱珠宝首饰有限公司 | Fading-resistant 18K black gold processing technology for jewelry |
| IT202200010889A1 (en) * | 2022-05-25 | 2023-11-25 | Patros S R L | Method for obtaining an object comprising titanium for jewellery, goldsmithing or costume jewelery and object thus obtained. |
Also Published As
| Publication number | Publication date |
|---|---|
| IT1240937B (en) | 1993-12-27 |
| IT9067023A1 (en) | 1991-07-12 |
| GB9014240D0 (en) | 1990-08-15 |
| GB2245590A (en) | 1992-01-08 |
| DE4020329A1 (en) | 1992-01-02 |
| FR2643649A1 (en) | 1990-08-31 |
| FR2643649B1 (en) | 1994-05-13 |
| CH680735A5 (en) | 1992-10-30 |
| IT9067023A0 (en) | 1990-01-12 |
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