GB2173218A - A metal-made article for personal ornament having coloured surface - Google Patents
A metal-made article for personal ornament having coloured surface Download PDFInfo
- Publication number
- GB2173218A GB2173218A GB08606672A GB8606672A GB2173218A GB 2173218 A GB2173218 A GB 2173218A GB 08606672 A GB08606672 A GB 08606672A GB 8606672 A GB8606672 A GB 8606672A GB 2173218 A GB2173218 A GB 2173218A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nickel
- layer
- palladium
- plating
- alloy
- 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
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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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/0015—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterized by the colour of the layer
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/0635—Carbides
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/0641—Nitrides
-
- 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/08—Oxides
- C23C14/083—Oxides of refractory metals or yttrium
-
- 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
- C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Electroplating Methods And Accessories (AREA)
Abstract
A coloured, strongly corrosion-resistant personal ornamental article of a copper alloy-made substrate body is prepared by providing the substrate surface with a triple coating composed of a first plating layer of nickel, then an intermediate plating layer of an alloy of palladium and nickel in a specific weight proportion and finally a coloured finish layer of a nitride, carbide or oxide selected from titanium, tantalum, zirconium, hafnium, chromium, molybdenum, niobium and vanadium.
Description
SPECIFICATION
A Metal-made Article for Personal Ornament Having Coloured Surface
The present invention relates to a metal-made article for personal ornament having an aesthetically acceptable and durably coloured surface. More particularly, the invention relates to a metal-made article of a copper alloy for personal ornament having a coloured surface by providing a multi-layered plating formed by utilizing the techniques of ion plating or sputtering.
As is known, various kinds of metal-made articles of copper alloys for personal ornament use are
provided with a coloured surface with an object to increase the aesthetic value thereof. For example, an article of a copper alloy is first provided with an underlying plating layer of nickel followed by a treatment of ion plating to form an overcoating layer of titanium nitride. An improvement for the above mentioned nickel- and titanium nitride-plated article of a copper alloy is proposed in Japanese Patent Kokai 60-70171, according to which an ornamental article of a copper alloy is first plated with nickel as an undercoating layer on which an intermediate plating layer is formed of palladium or rhodium and finally an overcoating finish
layer of titanium nitride is formed bythe method of ion plating or sputtering.
When comparison is made between an ornamental article of a copper-based alloy by the above described coating method of ion plating or sputtering to form a coloured layer of titanium nitride on the undercoating layer of nickel and a gold-plated article by the traditional plating method, the former is inferior to the latter in the following respects. Namely, the former article provided with the bilayer plating of nickel
and titanium nitride cannot have sufficient corrosion resistance and durability of colour since the coloured
layer of titanium nitride is usually so thin that no sufficient protection is provided to the underlying nickel
layer which is not free from pin holes susceptible to corrosion therethrough unless the nickel layer has a thickness of 10 um or larger.Such a large thickness of the nickel plating to achieve corrosion resistance is
necessarily accompanied by a problem in the appearance of finished articles since the aesthetic value of
decorative delicate patterns formed on the base article is greatly reduced with obscureness and dullness by the thick plating layer of nickel so that the method of increased thickness of the nickel layer cannot be applied to articles of high precision works.
The above mentioned improvement by forming an intermediate layer of palladium or rhodium to
provide a triply plated coating is indeed advantageous in respect of the corrosion resistance when the
intermediate layer has a considerably large thickness in comparison with the doubly plated coating of nickel
and titanium nitride. Ornamental articles triply plated with nickel, palladium or rhodium and titanium
nitride, however, are not without problems and disadvantages to be improved. For example, the corrosion
resistance of the article is still not quite satisfactory, in particular, when the thickness of the intermediate
layer is small. In addition, palladium metal, in particular, has a relatively low hardness of, for example, 300 to 400 HV so that the article is not free from a problem in the abrasion resistance required for articles of exterior ornament.The plating layer of palladium or rhodium is not sufficiently resistant against galvanic
corrosion due to the large potential difference thereof from nickel. Moreover, the rate of electrolytic
deposition of the plating layer of palladium or rhodium is relatively low and deposition of a palladium layer
of 1 pm thickness usually takes 7 to 10 minutes so that the intermediate layer of palladium or rhodium is
disadvantageous in respect of productivity even by setting aside the expensiveness of palladium or, in
particular, rhodium.
We have now found it possible to provide a copper alloy-made personal ornamental article provided with a coloured coating having high corrosion resistance equatable with that of gold plating without the above described problems and disadvantages in the prior art articles finished by ion plating or sputtering to form a layer of titanium nitride or other coloured finishing layer.
Thus, the personal ornamental article of the present invention provided with a coloured coating thereon comprises:
(a) a substrate made of a copper alloy;
(b) a first plating layer of nickel formed on the substrate and having a thickness in the range, preferably, from 1 to 10 pm; (c) an intermediate plating layer of an alloy of nickel and palladium in a weight proportion of palladium to nickel in the range from 50:50 to 90:10 or, preferably, from 55:45 to 65::35 formed on the first layer of
nickel and having a thickness in the range, preferably, from 0.5 to 5 pm; and
(d) a finish layer of a nitride, carbide or oxide of a metal or a mixture thereof having a thickness in the
range, preferably, from 0.1 to 2.0 lim formed on the intermediate layer of nickel-palladium alloy by the
method of ion plating or sputtering, the metal being selected from the group consisting of titanium, tantalum, zirconium, chromium, hafnium, molybdenum, niobium and vanadium.
As is understood from the above given summarizing description, the personal ornamental article of the
invention has a triple-layered coating on the surface composed of a first layer of nickel, an intermediate
layer of a nickel-palladium alloy and a finish layer of the above mentioned nitride, carbide and/or oxide of a
metal such us titanium nitride. The most characteristic feature of the invention is in the intermediate layer which is, different from the conver,;ional intermediate plating layer of palladium or rhodium alone, made of
an alloy of nickel and palladium in a specific alloying proportion.
By virtue of this unique feature in the coating, the ornamental article of the invention has several
advantages over conventional ones including the high abrasion resistance suitable as an exterior ornament with only a tenth or less of wearing in comparison with the articles provided with an intermediate layer of palladium alone as a result of the high hardness of the nickel-palladium alloy in the range from 500 to 600
HV, high resistance against galvanic corrosion as a result of the proximity in the potential difference, outstandingly high rate of electrolytic deposition of the alloy taking, usually, only 4 minutes for the deposition of a 1 pm thick layer.
The figure in the accompanying drawing schematically illustrates a partial cross section of the inventive article as cut perpendicularly to the surface, in which the substrate body 1 of the ornamental article made of a copper alloy is coated with a first plating layer 2 of nickel, then an intermediate layer 3 of an alloy of palladium and nickel and finally a finish layer 4 of a nitride, carbide and/or oxide of the above specified metal or a mixture thereof, each layer preferably having a specified thickness.
The substrate body of the inventive ornamental article should be made of a copper alloy although any body made of other materials can be used provided that a substrate base coating or plating layer of a copper alloy is formed beforehand on the surface. The copper alloy here implied is not particularly limitative and includes brass, bronze, German silver and the like provided that the major constituent thereof is copper.
The substrate body of copper alloy is pretreated in a conventional manner by washing with an organic solvent, e.g. trichloroethylene, degreasing with an alkali and neutralization with an acid followed by thorough rinse with water prior to nickel plating. The nickel plating is performed, preferably, eiectrolytically according to a known procedure. The formulation of the electrolytic plating bath and the electrolytic conditions are well known in the art. Following are the typical bath formulation and electrolytic conditions used in an example.
Electrolytic Plating Bath:
Nickel sulphate 250 g/litre
Nickel chloride 50 g/litre
Boric acid 40 g/litre
Non-leveling agent (Hi-nickel i200, a trade name by Shimizu Shoji Co.) 15 ml/litre
Electrolytic Conditions:
Current density 5Aldm2 Bath temperature 45"C Length oftime 3 minutes
When the electrolytic nickel plating is performed in the plating bath and under the conditions specified above, a nickel plating layer having a thickness of about 3 pm is obtained although the thickness thereof can be in the range from 1 to 10 pm. When the thickness of the nickel plating is smaller than 1 pm, no satisfactory corrosion resistance can be obtained while a nickel plating layer having a thickness larger than 10 lim is undesirable in respect of the decreased productivity and loss of decorativeness in fine and delicately designed patterns.
When the first electrolytic plating procedure is completed in the above described manner, the nickel-plated substrate body is thoroughly rinsed with water and transferred into a second electrolytic plating bath for the intermediate layer of a palladium-nickel alloy. Typical formulation of the electrolytic bath and the electrolytic conditions are as follows.
Electrolytic Plating Bath:
Palladium ammine complex (as Pd) 8 g/litre
Nickel chloride (as Ni) 8 g/litre
Ammonium chloride 100 g/litre
Brightening agents (Udylites
610, 62 and 63, trade names) each 1-20 ml/litre
pH 7.8
Electrolytic Conditions:
Current density 1.0 A/dm2
Bath temperature room temperature
Length of time 12 minutes
When the electrolytic plating is performed in the bath and under the conditions specified above, a coating layer of a palladium-nickel alloy composed of about 80% by weight of palladium and about 20% by weight of nickel having a thickness of about 3 pn ì is formed on the surface of the underlying nickel plating although the alloy composition and the thickness of the plating layer are not particularly limited to the above.For example, the thickness of the palladium-nickel alloy should be in the range from 0.5 to 5 pm.
When the thickness is smaller than 0.5 pom, no satisfactory corrosion resistance can be obtained while a thickness largerthan 5pm is undesirable mainlyforan economical reason.
The final step to prepare the inventive ornamental article is the ion plating or sputtering to form a
coloured finish layer of a nitride, carbide or oxide of a metal or a mixture thereof on the intermediate layer
of the palladium-nickel alloy, which can be performed according to a known procedure. In the case of ion
plating, for example, the ornamental article after completion of the second electrolytic plating to form the
intermediate layer of a palladium-nickel alloy is placed in a bell jar of an apparatus for ion plating and
cleaned by ion bombardment in low-pressure argon.Thereafter, a gaseous mixture of argon as an inert
carrier gas and, assuming that the desired finish layer is of a metal nitride, nitrogen as a reactive gas is
introduced into the bell jar under continuous evacuation to control and maintain the pressure inside at about 2.0x10-3 Torr and an electric power of 3.0 kV is impressed between the electrodes to generate
plasma inside the bell jar so that the metal, e.g. titanium, tantalum, niobium and the like, in a boat below is
vapourized so as to deposit the metal vapor on the surface of the palladium-nickel alloy layer on the
substrate body in the form of the metal nitride. In this manner, a beautiful golden-brig ht yellow finish is
obtained on the substrate body when the finish layer is of titanium nitride.The techniques of sputtering are
also well known in the art so that no detailed description is given here. The colour can be modified by
suitably selecting the kinds of the metal and the reactive gas as is mentioned below.
When the nitrogen as the reactive gas is replaced with a carbon-containing gas such as acetylene,
ethylene, methane and the like or an oxygen or oxygen-containing gas, the layer of the finish coating
formed by the ion plating can be of a carbide or oxide of the metal having an aesthetically acceptable colour
other than golden-bright yellow. It is of course that use of a gaseous mixture of two types of reactive gases
may result in the formation of a finish coating made of a mixture of nitride, carbide and oxide by the ion
plating or sputtering.
EXAMPLE 1
With an object to make a comparison of the corrosion resistance between the articles according to the
invention and those according to conventional methods, brass-made substrate bodies were provided first
with a layer of nickel plating having a varied thickness of 1 to 10 pm and then with an intermediate layer of a
palladium-nickel alloy having a thickness of 0.5 or 3 um according to the typical bath formulations and
electrolytic conditions shown before followed by finishing in an ion plating procedure to form a finish layer
of titanium nitride having a thickness of 0.5 pm. Comparative test specimens finished by ion plating to form
a titanium nitride layer were prepared by omitting the intermediate layer or by providing an intermediate
layer of palladium alone instead of the palladium-nickel alloy. In addition, further comparative specimens
were prepared by gold plating according to the GP3 p specification of a 1 pm layer of 18K Au/Ag plus 2 pm layer of 22K Au/Ni on an underlying nickel plating of 3 pm thickness. The number of the test specimens
prepared for each combination of the types of the layers and the values of thickness thereof was 100.
The test specimens prepared in the above described manner were subjected to the test of corrosion
resistance by dipping in a simulated perspiration according to the specification of ISO 3160/2 7-4 for 24 hours to give the results shown in Table 1 below, in which the corrosion resistance was given by 4 ratings of
A, B, C and D according to the number of etched spots on the surface, the grades A and D corresponding to absolute absence of any changes and unacceptably poor corrosion resistance, respectively.
EXAMPLE 2
To make a further comparison, the same experimental procedure as above was repeated except that
the finish layeroftitanium nitride was replaced with a layeroftitanium carbide formed by the techniques of
ion plating in which the reactive gas was ethylene in place of nitrogen and the gaseous pressure was kept at
3.5x 10-3 Torr and the voltage of the electric power was 7.0 kV. The finished test specimens were each
coloured in beautiful grey.The test specimens including those of the present invention and of the prior art
as well as the gold-plated ones were subjected to the test of corrosion resistance in the same manner as
above to give substantially the same conclusion that the coated ornamental articles according to the
invention are much superior to those of the prior art and comparable to those of the gold-plated ones in
respect of the corrosion resistance.
TABLE 1
Thickness of Corrosion Resistance,
Layers, pm Number of Test Pieces
Overall
Nickel Plating Intermediate Layer A B C D Evaluation 0.5 (Pd/Ni) 99 1 0 0 Good
1 3(Pd/Ni) 100 0 0 0 Good
3 0.5 (Pd/Ni) 97 3 0 o Good
Present
invention 3 3 (Pd/Ni) 100 0 0 0 Good
5 0.5 (Pd/Ni) 99 1 0 0 Good
5 3 (Pd/Ni) 100 0 0 0 Good
10 0.5 (Pd/Ni) 99 1 0 0 Good
1 - 77 9 9 5 Poor
3 - 84 8 5 3 Poor
5 - 90 6 3 1 Poor
Prior art
10 - 95 4 1 0 Poor 3 0.3 (Pd) 93 .5 5 2 0 Fair 6 0.3 (Pd) 96 3 1 0 Fair
Gold 3 3 (GP3,u) 100 0 0 0 Good
plating
EXAMPLE 3
The nickel plating for the underlying layer and plating of a palladium-nickel alloy as the intermediate layer was performed in substantially the same manner as in Example 1 and a finish layer of a hafnium nitride was provided thereon by placing the substrate article in the bell jar of the ion-plating apparatus and cleaned by ion bombardment in an atmosphere of argon followed by introducing nitrogen gas at a rate of 20 ml/minute to maintain the pressure inside at lx 10-3 Torr and impression of a direct current voltage of 500 V between the substrate and the hafnium metal in a boat placed below while the hafnium metal was evaporated with electron beams.The hafnium nitride layer thus formed had a thickness of about 1.0 m pm and the article was coloured in beautiful blue. The corrosion resistance of the thus treated articles was as good as the articles prepared in Example 1 according to the invention.
EXAMPLE 4
The experimental procedure was substantially the same as in Example 1 except that the finish layer of titanium nitride was formed by the method of sputtering. Thus, the substrate article of a copper alloy provided with the first plating layer of nickel and the intermediate plating layer of the palladium-nickel alloy was placed in a bell jar into which, after ion bombardment of the article in an argon atmosphere, nitrogen gas was introduced at a rate of 20 ml/minute to keep the pressure inside at 5x 10-3 Torr, and a direct current voltage of 500 V was impressed between the article and the titanium metal in a boat below by the direct-current magnetron method. The thus prepared article provided with a finish layer of titanium nitride was golden yellow in colour and the corrosion resistance thereof was as good as those prepared in Example 1 according to the invention.
Claims (4)
1. A coloured personal ornamental article which comprises:
(a) a substrate made of a copper alloy;
(b) a first plating layer of nickel formed on the surface of the substrate and having a thickness in the range from 1 to 10pom; (c) an intermediate plating layer of an alloy of nickel and palladium in a weight proportion of palladium to nickel in the range from 50:50 to 90:10 formed on the first plating layer of nickel and having a thickness in the range from 0.5 to 5 pm; and
(d) a finish layer of a coloured nitride, carbide or oxide of a metal or a mixture thereof having a
thickness in the range from 0.1 to 2.0 pm formed on the intermediate plating layer of the palladium-nickel
alloy by the method of ion plating or sputtering, the metal being selected from the group consisting of
titanium, tantalum, zirconium, chromium, hafnium, molybdenum, niobium and vanadium.
2. The coloured personal ornamental article according to claim 1 wherein the intermediate plating layer
is formed of an alloy of palladium and nickel in a weight ratio in the range from 55:45 to 65:35.
3. An article according to claim 1 substantially as herein described.
4. Each and every novel product, process, method, apparatus, feature and combination substantially as
herein disclosed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7221085A JPH062935B2 (en) | 1985-04-05 | 1985-04-05 | Jewelry that has a colored surface |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8606672D0 GB8606672D0 (en) | 1986-04-23 |
GB2173218A true GB2173218A (en) | 1986-10-08 |
GB2173218B GB2173218B (en) | 1989-01-18 |
Family
ID=13482648
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08606672A Expired GB2173218B (en) | 1985-04-05 | 1986-03-18 | Personal ornamental article |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPH062935B2 (en) |
GB (1) | GB2173218B (en) |
HK (1) | HK37190A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0322812A2 (en) * | 1987-12-31 | 1989-07-05 | Air Products And Chemicals, Inc. | Hard outer coatings deposited on titanium or titanium alloys |
GB2226334A (en) * | 1988-11-25 | 1990-06-27 | Atomic Energy Authority Uk | Multilayer coatings |
EP0875601A1 (en) * | 1997-04-30 | 1998-11-04 | Masco Corporation | Coated article |
EP0875599A1 (en) * | 1997-04-30 | 1998-11-04 | Masco Corporation | Coated article |
EP0875600A1 (en) * | 1997-04-30 | 1998-11-04 | Masco Corporation | Coated article |
FR2762852A1 (en) * | 1997-04-30 | 1998-11-06 | Masco Corp | ARTICLE COATED WITH POLISHED BRASS COLORED MULTI-LAYER COATING FOR PROTECTION AGAINST ABRASION AND CORROSION |
US5868912A (en) * | 1993-11-22 | 1999-02-09 | E. I. Du Pont De Nemours And Company | Electrochemical cell having an oxide growth resistant current distributor |
DE19809408A1 (en) * | 1998-03-05 | 1999-09-09 | Leybold Systems Gmbh | Brass-colored coating with a coloring nitridic layer |
EP1033416A1 (en) * | 1999-03-01 | 2000-09-06 | Moen Incorporated | Decorative corrosion and abrasion resistant coating |
US6413653B1 (en) | 1998-08-03 | 2002-07-02 | Citizen Watch Co., Ltd. | Personal ornament covered with colored coating and process for producing the same |
US7396595B2 (en) | 2001-09-19 | 2008-07-08 | Citizen Holdings Co., Ltd. | Soft metal and method for preparation thereof, and exterior part of watch and method for preparation thereof |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61176256U (en) * | 1985-04-19 | 1986-11-04 | ||
US6106958A (en) * | 1997-04-30 | 2000-08-22 | Masco Corporation | Article having a coating |
US6004684A (en) * | 1997-04-30 | 1999-12-21 | Masco Corporation | Article having a protective and decorative multilayer coating |
JP2007270276A (en) * | 2006-03-31 | 2007-10-18 | Shimano Inc | Parts for outdoor use |
JP6046406B2 (en) * | 2011-07-26 | 2016-12-14 | ローム アンド ハース エレクトロニック マテリアルズ エルエルシーRohm and Haas Electronic Materials LLC | High temperature resistant silver coated substrate |
CN109652838B (en) * | 2018-12-27 | 2021-05-18 | 浙江工业大学 | Titanium-niobium alloy surface anodic oxidation coloring method |
-
1985
- 1985-04-05 JP JP7221085A patent/JPH062935B2/en not_active Expired - Fee Related
-
1986
- 1986-03-18 GB GB08606672A patent/GB2173218B/en not_active Expired
-
1990
- 1990-05-17 HK HK37190A patent/HK37190A/en not_active IP Right Cessation
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0322812A2 (en) * | 1987-12-31 | 1989-07-05 | Air Products And Chemicals, Inc. | Hard outer coatings deposited on titanium or titanium alloys |
EP0322812A3 (en) * | 1987-12-31 | 1989-11-08 | Air Products And Chemicals, Inc. | Hard outer coatings deposited on titanium or titanium alloys |
GB2226334A (en) * | 1988-11-25 | 1990-06-27 | Atomic Energy Authority Uk | Multilayer coatings |
US5868912A (en) * | 1993-11-22 | 1999-02-09 | E. I. Du Pont De Nemours And Company | Electrochemical cell having an oxide growth resistant current distributor |
FR2762856A1 (en) * | 1997-04-30 | 1998-11-06 | Masco Corp | ARTICLE HAVING A DECORATIVE AND PROTECTIVE COATING |
EP0875600A1 (en) * | 1997-04-30 | 1998-11-04 | Masco Corporation | Coated article |
FR2762854A1 (en) * | 1997-04-30 | 1998-11-06 | Masco Corp | ARTICLE COATED WITH A COLORED MULTI-LAYER COATING OF POLISHED BRASS, PROVIDING PROTECTION AGAINST ABRASION AND CORROSION |
FR2762852A1 (en) * | 1997-04-30 | 1998-11-06 | Masco Corp | ARTICLE COATED WITH POLISHED BRASS COLORED MULTI-LAYER COATING FOR PROTECTION AGAINST ABRASION AND CORROSION |
EP0875599A1 (en) * | 1997-04-30 | 1998-11-04 | Masco Corporation | Coated article |
FR2762858A1 (en) * | 1997-04-30 | 1998-11-06 | Masco Corp | ARTICLE HAVING A DECORATIVE AND PROTECTIVE COATING |
EP0875601A1 (en) * | 1997-04-30 | 1998-11-04 | Masco Corporation | Coated article |
DE19809408A1 (en) * | 1998-03-05 | 1999-09-09 | Leybold Systems Gmbh | Brass-colored coating with a coloring nitridic layer |
US6413653B1 (en) | 1998-08-03 | 2002-07-02 | Citizen Watch Co., Ltd. | Personal ornament covered with colored coating and process for producing the same |
EP1033416A1 (en) * | 1999-03-01 | 2000-09-06 | Moen Incorporated | Decorative corrosion and abrasion resistant coating |
US6245435B1 (en) | 1999-03-01 | 2001-06-12 | Moen Incorporated | Decorative corrosion and abrasion resistant coating |
US7396595B2 (en) | 2001-09-19 | 2008-07-08 | Citizen Holdings Co., Ltd. | Soft metal and method for preparation thereof, and exterior part of watch and method for preparation thereof |
CN100503891C (en) * | 2001-09-19 | 2009-06-24 | 西铁城控股株式会社 | Soft metal and method for preparation thereof, and exterior part of watch and method for preparation thereof |
Also Published As
Publication number | Publication date |
---|---|
GB2173218B (en) | 1989-01-18 |
HK37190A (en) | 1990-05-25 |
GB8606672D0 (en) | 1986-04-23 |
JPH062935B2 (en) | 1994-01-12 |
JPS61231164A (en) | 1986-10-15 |
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Legal Events
Date | Code | Title | Description |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20010318 |