US20080156652A1 - Cyanide-free pre-treating solution for electroplating copper coating layer on zinc alloy surface and a pre-treating method thereof - Google Patents
Cyanide-free pre-treating solution for electroplating copper coating layer on zinc alloy surface and a pre-treating method thereof Download PDFInfo
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- US20080156652A1 US20080156652A1 US11/646,976 US64697606A US2008156652A1 US 20080156652 A1 US20080156652 A1 US 20080156652A1 US 64697606 A US64697606 A US 64697606A US 2008156652 A1 US2008156652 A1 US 2008156652A1
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- copper
- treating solution
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- zinc alloy
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- 229910001297 Zn alloy Inorganic materials 0.000 title claims abstract description 43
- 238000009713 electroplating Methods 0.000 title claims abstract description 38
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 33
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 33
- 239000010949 copper Substances 0.000 title claims abstract description 33
- 239000011247 coating layer Substances 0.000 title claims abstract description 18
- 238000000034 method Methods 0.000 title claims description 31
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000000654 additive Substances 0.000 claims abstract description 17
- 230000000996 additive effect Effects 0.000 claims abstract description 17
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910001431 copper ion Inorganic materials 0.000 claims abstract description 15
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 13
- 150000003839 salts Chemical class 0.000 claims abstract description 12
- 239000008139 complexing agent Substances 0.000 claims abstract description 11
- -1 hydroxyl ions Chemical class 0.000 claims abstract description 10
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910001379 sodium hypophosphite Inorganic materials 0.000 claims abstract description 7
- 239000001488 sodium phosphate Substances 0.000 claims abstract description 7
- 229910000162 sodium phosphate Inorganic materials 0.000 claims abstract description 7
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical group [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims abstract description 7
- 229910000365 copper sulfate Inorganic materials 0.000 claims abstract description 6
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims abstract description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 239000013527 degreasing agent Substances 0.000 claims description 6
- 238000005237 degreasing agent Methods 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims description 5
- 235000011006 sodium potassium tartrate Nutrition 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 229940074439 potassium sodium tartrate Drugs 0.000 claims description 4
- 235000002906 tartaric acid Nutrition 0.000 claims description 4
- 239000011975 tartaric acid Substances 0.000 claims description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 3
- 239000000908 ammonium hydroxide Substances 0.000 claims description 3
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 3
- 238000005238 degreasing Methods 0.000 claims description 3
- PEVJCYPAFCUXEZ-UHFFFAOYSA-J dicopper;phosphonato phosphate Chemical compound [Cu+2].[Cu+2].[O-]P([O-])(=O)OP([O-])([O-])=O PEVJCYPAFCUXEZ-UHFFFAOYSA-J 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- AVTYONGGKAJVTE-OLXYHTOASA-L potassium L-tartrate Chemical compound [K+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O AVTYONGGKAJVTE-OLXYHTOASA-L 0.000 claims description 3
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 claims description 3
- 229940111695 potassium tartrate Drugs 0.000 claims description 3
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 claims description 3
- 239000001433 sodium tartrate Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- 229910002804 graphite Inorganic materials 0.000 claims description 2
- 239000010439 graphite Substances 0.000 claims description 2
- 150000004677 hydrates Chemical class 0.000 claims description 2
- 239000001472 potassium tartrate Substances 0.000 claims description 2
- 235000011005 potassium tartrates Nutrition 0.000 claims description 2
- 229960002167 sodium tartrate Drugs 0.000 claims description 2
- 235000011004 sodium tartrates Nutrition 0.000 claims description 2
- 229910001220 stainless steel Inorganic materials 0.000 claims description 2
- 239000010935 stainless steel Substances 0.000 claims description 2
- 229960001367 tartaric acid Drugs 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 abstract description 14
- 239000010410 layer Substances 0.000 abstract description 12
- 231100000331 toxic Toxicity 0.000 abstract description 8
- 230000002588 toxic effect Effects 0.000 abstract description 8
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002966 varnish Substances 0.000 abstract description 5
- 229910052751 metal Inorganic materials 0.000 abstract description 3
- 239000002184 metal Substances 0.000 abstract description 3
- 230000008719 thickening Effects 0.000 abstract description 3
- 238000007599 discharging Methods 0.000 abstract description 2
- 238000011282 treatment Methods 0.000 description 10
- 238000002203 pretreatment Methods 0.000 description 7
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 4
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000007772 electroless plating Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 2
- 229940117975 chromium trioxide Drugs 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 238000000386 microscopy Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- QPJSUIGXIBEQAC-UHFFFAOYSA-N n-(2,4-dichloro-5-propan-2-yloxyphenyl)acetamide Chemical compound CC(C)OC1=CC(NC(C)=O)=C(Cl)C=C1Cl QPJSUIGXIBEQAC-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000001476 sodium potassium tartrate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/10—Electroplating with more than one layer of the same or of different metals
- C25D5/12—Electroplating with more than one layer of the same or of different metals at least one layer being of nickel or chromium
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/34—Pretreatment of metallic surfaces to be electroplated
Definitions
- the present invention relates to a pre-treating solution, and more particularly to a pre-treating solution without toxic materials.
- a pre-treating method of the pre-treating solution is also disclosed.
- Zinc alloy is composed of zinc in majority and other additive elements and is active in chemical reacting property so that its application can not extended. Because the zinc alloy is insufficient in anti-corrosion capability, surface treatment of the zinc alloy is particularly important.
- Conventional surface treatment of zinc alloy includes anodic treatment, synthesizing treatment and metal-coating treatment (e.g. nickel-coating treatment) etc.
- anodic treatment and synthesizing treatment are to create an anti-corrosion oxide layer on surface of the zinc alloy but the oxide layer has insufficient corrosion resistance and needs further processes such as paint-spraying to achieve anti-corrosion purposes.
- the metal-coating treatment not only significantly improves corrosion resistance of the zinc alloy but also increases hardness, abrasion resistance and appearance varnish.
- the metal-coating treatment on the zinc alloy is carried out by electroless plating method that is time-consuming and has complex pre-treatments.
- solvents used in the pre-treatments mostly contain toxic acidic materials such as hydrofluoric acid (HF) and chromium trioxide (CrO 3 ) and cyanide.
- HF hydrofluoric acid
- CrO 3 chromium trioxide
- the complex pre-treatments cause cost increment and the toxic materials may cause damage to environments and human being.
- another optional electroplating method can save more time than the electroless plating method, the electroplating method on the zinc alloy is at a developing stage and not matured enough so that yield is poor.
- a critical disadvantage of the electroplating method is that corrosion happens easily on surface of the zinc alloy no matter in acid or alkaline electroplating solutions.
- the market-available electroplating solution can not directly use in the electroplating method of zinc alloy.
- the electroless plating method generates a non-conductive layer on the surface of the zinc alloy and thus can not be applied as a pre-treatment of the electroplating method.
- the present invention has arisen to mitigate and/or obviate the drawbacks of the conventional electroplating solutions and methods for electroplating the zinc alloy.
- the main objective of the present invention is to provide a cyanide-free pre-treating solution for electroplating zinc alloy surface, wherein the pre-treating solution is non-toxic and enables its operational methods to be simplified.
- Another main objection of the present invention is to provide operational methods that make use of the above pre-treating solution for electroplating zinc alloy surface.
- the cyanide-free pre-treating solution comprises an aqua solution added with copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from the group consisting of sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid or hypophosphite acid.
- the operational method comprises steps of:
- the pre-treating solution contains no toxic materials such as cyanide etc.
- the pre-treating solution is safe and environmental during treatment of the zinc alloy surface.
- the pre-treating method using the pre-treating solution facilitates the further nickel-coating treatment of the zinc alloy.
- FIG. 1 is a flow chart of a pre-treatment of zinc alloy using a cyanide-free pre-treating solution in accordance with the present invention
- FIG. 2 is a SEM (Scanning Electronic Microscopy) picture showing a first copper coating layer on surface of the zinc alloy
- FIG. 3 is a SEM (Scanning Electronic Microscopy) picture further showing a second copper coating layer laminated on the first copper layer in FIG. 2 .
- a pre-treating solution for electroplating zinc alloy surface in accordance with the present invention contains copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid or hypophosphite acid.
- the zinc alloy is dipped in the pre-treating solution and electroplated with a first copper coating layer. Then, the zinc alloy is further dipped in a market-available copper sulfate solution for thickening the copper coating layer (performing a second copper coating layer) and lastly coated with an anti-corrosion metal layer.
- the pre-treating solution contains no cyanide and thus is low toxic and safe to operator during electroplating and to environment after discharging.
- the pre-treating solution for electroplating zinc alloy surface comprises: 3 to 50 g/L of copper ions obtained from copper chloride, copper sulfate, or copper pyrophosphate; 5 to 30 g/L of hydroxyl ions obtained from sodium hydroxide, potassium hydroxide, or ammonium hydroxide; 25 to 150 g/L of the complexing agent selected from the group consisting of potassium sodium tartrate, potassium tartrate and sodium tartrate; and 5 to 50 g/L of the additive selected from the group consisting of sodium phosphate, sodium hypophosphite and phosphoric acid.
- the pre-treating solution can be modified to have different preferred compositions as shown in following table:
- Copper ion Hydroxyl ion agent additive 1 3.5 g/L 5 g/L 57 g/L 15 g/L 2 5.7 g/L 9.1 g/L 27.3 g/L 2 g/L 3 3.2 g/L 17.3 g/L 66.9 g/L 5 g/L 4 6.2 g/L 8 g/L 27.9 g/L 1.7 g/L 5 5.4 g/L 30 g/L 65 g/L 14.7 g/L 6 6.4 g/L 8.6 g/L 30.9 g/L 1 g/L 7 5.9 g/L 7.7 g/L 26.4 g/L 1.8 g/L 8 13.7 g/L 22.3 g/L 67.8 g/L 3.3 g/L 9 14.6 g/L 25.8 g/L 45.3 g/L 3.2 g/L 10 15.1 g/L 27.4 g/L
- compositions of the pre-treating solution in serial number of 2, 4, 6, 7, 11, 13, 17 and 20 in the table are mostly preferred.
- a pre-treating operation to the zinc alloy is shown and is adapted to form a first copper coating layer on a prepared workpiece made of the zinc alloy by using the pre-treating solution in the present invention.
- the pre-treating operation comprises steps of:
- the prepared workpiece is degreased with a degreasing agent to remove oil and dirt from its surface.
- the prepared workpiece is washed to remove the degreasing agent and to keep the surface clean.
- the workpiece is dipped into the pre-treating solution with auxiliary electrodes and electroplated to obtain a copper coating layer (the first copper coating layer) thereon by applying a fixed current from an additional power supplier.
- a washing step is added into the pre-treating method after the (c) step of copper electroplating.
- the surface temperature of the workpiece in (c) step of copper electroplating is about 10 to 90° C.
- the fixed current provided by the additional power supplier has a range from 0.002 to 0.02 ampere per square decimeter.
- the auxiliary electrodes are made of material selected from the group comprising titanium core coated with platinum, titanium, platinum, graphite and stainless steel.
- a preferred embodiment of a pre-treating operation is shown.
- the workpiece is prepared ( 10 ), degreased ( 11 ) and washed ( 12 ) to make its surface clean.
- the workpiece, auxiliary electrodes, and the pre-treating solution are inputted into a tank to carry out electroplating ( 13 ) with mechanically stir.
- the copper ions in the pre-treating solution obtain electrons to reduce and deposit on the surface of the workpiece so that the workpiece obtains a uniform copper coating layer, i.e. the first copper coating layer.
- the workpiece is washed ( 14 ) again and dried ( 15 ) to obtain the final product.
- the workpiece with the first copper coating layer is further treated with a conventional electroplating process to form a second copper coating layer on the first copper coating layer to obtain the final product.
- the workpiece is further coated with an anti-corrosion metal layer to have excellent anti-corrosion and anti-wearing efficiency and varnish appearance.
- the substrate ( 20 ) of the zinc alloy is coated with a uniform first copper layer ( 21 ) after inputting the substrate ( 20 ), the auxiliary electrodes and the pre-treating solution into the tank and carrying out electroplating with mechanically stir by applying a fixed current from the additional power supplier. Thereby, the surface of the zinc alloy substrate ( 20 ) becomes brownish in appearance.
- the zinc alloy having the first copper layer ( 21 ) is further treated with conventional electroplating by use of market-available copper sulfate solution to form a second copper layer ( 22 ) for thickening.
- the zinc alloy is further treated with an anti-corrosion electroplating to perform a nickel coating (not shown) thereon so that the surface of the zinc alloy is corrosion-resistant and wearing-resistant and has a varnish appearance.
- the cyanide-free pre-treating solution for zinc alloy surface contains an aqua solution added with copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid and hypophosphite acid.
- the copper ions are obtained from copper chloride, copper sulfate, copper pyrophosphate or hydrates of foregoing mentioned salts.
- concentration of the copper ion is 3 to 50 g/L.
- the complexing agent is selected from potassium sodium tartrate, potassium tartrate, sodium tartrate, tartaric acid, and dissolvable salts derivative from tartaric acid.
- concentration of the complexing agent is 10 to 150 g/L.
- concentration of the additive is 1 to 50 g/L.
- hydroxyl ions are obtained from sodium hydroxide, potassium hydroxide, ammonium hydroxide or dissolvable salts of alkaline.
- concentration of the hydroxyl ion is 5 to 30 g/L.
- the cyanide-free pre-treating solution for zinc alloy surface in accordance with the present invention and its operational method has the following advantages:
- the conventional electroless method is troublesome in pre-treatment.
- the pre-treating solution with copper ions to carry the pre-treatment out, the following nickel layer can be efficiently applied onto the copper layer so that the active zinc alloy surface is completely treated with rapidly and simply two-step electroplating procedures.
- the pre-treating solution in the present invention is alkaline in particular and contains no toxic cyanide, hydrofluoric acid (HF) and chromium trioxide (CrO 3 ) so that it is safe to human being and environment and causes no pollution during electroplating procedures.
- HF hydrofluoric acid
- CrO 3 chromium trioxide
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemically Coating (AREA)
Abstract
A pre-treating solution for electroplating zinc alloy surface contains copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts of phosphoric acid. The zinc alloy is dipped in the pre-treating solution and electroplated with a copper coating layer. Then, the zinc alloy is further dipped in a copper sulfate solution for thickening the copper coating layer and lastly coated with an anti-corrosion metal layer. Thereby, zinc alloy has excellent anti-corrosion and anti-wearing efficiency and varnish appearance. Moreover, the pre-treating solution contains no cyanide and thus is low toxic and safe to operator during electroplating and to environment after discharging.
Description
- 1. Field of the Invention
- The present invention relates to a pre-treating solution, and more particularly to a pre-treating solution without toxic materials. A pre-treating method of the pre-treating solution is also disclosed.
- 2. Description of Related Art
- Zinc alloy is composed of zinc in majority and other additive elements and is active in chemical reacting property so that its application can not extended. Because the zinc alloy is insufficient in anti-corrosion capability, surface treatment of the zinc alloy is particularly important. Conventional surface treatment of zinc alloy includes anodic treatment, synthesizing treatment and metal-coating treatment (e.g. nickel-coating treatment) etc. Wherein, anodic treatment and synthesizing treatment are to create an anti-corrosion oxide layer on surface of the zinc alloy but the oxide layer has insufficient corrosion resistance and needs further processes such as paint-spraying to achieve anti-corrosion purposes. The metal-coating treatment not only significantly improves corrosion resistance of the zinc alloy but also increases hardness, abrasion resistance and appearance varnish.
- The metal-coating treatment on the zinc alloy is carried out by electroless plating method that is time-consuming and has complex pre-treatments. Moreover, solvents used in the pre-treatments mostly contain toxic acidic materials such as hydrofluoric acid (HF) and chromium trioxide (CrO3) and cyanide. The complex pre-treatments cause cost increment and the toxic materials may cause damage to environments and human being. Although another optional electroplating method can save more time than the electroless plating method, the electroplating method on the zinc alloy is at a developing stage and not matured enough so that yield is poor. A critical disadvantage of the electroplating method is that corrosion happens easily on surface of the zinc alloy no matter in acid or alkaline electroplating solutions. Therefore, the market-available electroplating solution can not directly use in the electroplating method of zinc alloy. Moreover, the electroless plating method generates a non-conductive layer on the surface of the zinc alloy and thus can not be applied as a pre-treatment of the electroplating method.
- Additionally, two conventional electroplating methods for zinc alloy are also concerned, one is chemical electroplating that takes formaldehyde as catalyst and the other is current electroplating that applies current to reduce copper ions, wherein the copper cyanide is toxic and acidic.
- Therefore, the present invention has arisen to mitigate and/or obviate the drawbacks of the conventional electroplating solutions and methods for electroplating the zinc alloy.
- The main objective of the present invention is to provide a cyanide-free pre-treating solution for electroplating zinc alloy surface, wherein the pre-treating solution is non-toxic and enables its operational methods to be simplified.
- Another main objection of the present invention is to provide operational methods that make use of the above pre-treating solution for electroplating zinc alloy surface.
- To achieve foregoing main objectives, the cyanide-free pre-treating solution comprises an aqua solution added with copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from the group consisting of sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid or hypophosphite acid.
- The operational method comprises steps of:
- (a) degreasing: a prepared workpiece made of zinc alloy is degreased with a degreasing agent to remove oil and dirt from surface of the prepared workpiece;
- (b) washing: the prepared workpiece is washed to remove the degreasing agent and to keep the surface of the prepared workpiece clean;
- (c) copper electroplating: the prepared workpiece is dipped into the pre-treating solution with auxiliary electrodes and electroplated to obtain a copper coating layer by applying a fixed current from an additional power supplier; and
- (d) drying: the pre-treating solution residual on the prepared workpiece is removed from the surface of the workpiece to make the surface dry rapidly.
- Because the pre-treating solution contains no toxic materials such as cyanide etc., the pre-treating solution is safe and environmental during treatment of the zinc alloy surface. Moreover, the pre-treating method using the pre-treating solution facilitates the further nickel-coating treatment of the zinc alloy.
- Further benefits and advantages of the present invention will become apparent after a careful reading of the detailed description with appropriate reference to the accompanying drawings.
-
FIG. 1 is a flow chart of a pre-treatment of zinc alloy using a cyanide-free pre-treating solution in accordance with the present invention; -
FIG. 2 is a SEM (Scanning Electronic Microscopy) picture showing a first copper coating layer on surface of the zinc alloy; and -
FIG. 3 is a SEM (Scanning Electronic Microscopy) picture further showing a second copper coating layer laminated on the first copper layer inFIG. 2 . - A pre-treating solution for electroplating zinc alloy surface in accordance with the present invention contains copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid or hypophosphite acid. The zinc alloy is dipped in the pre-treating solution and electroplated with a first copper coating layer. Then, the zinc alloy is further dipped in a market-available copper sulfate solution for thickening the copper coating layer (performing a second copper coating layer) and lastly coated with an anti-corrosion metal layer. Thereby, zinc alloy has excellent anti-corrosion and anti-wearing efficiency and varnish appearance. Moreover, the pre-treating solution contains no cyanide and thus is low toxic and safe to operator during electroplating and to environment after discharging.
- The pre-treating solution for electroplating zinc alloy surface comprises: 3 to 50 g/L of copper ions obtained from copper chloride, copper sulfate, or copper pyrophosphate; 5 to 30 g/L of hydroxyl ions obtained from sodium hydroxide, potassium hydroxide, or ammonium hydroxide; 25 to 150 g/L of the complexing agent selected from the group consisting of potassium sodium tartrate, potassium tartrate and sodium tartrate; and 5 to 50 g/L of the additive selected from the group consisting of sodium phosphate, sodium hypophosphite and phosphoric acid. Reasonably, the pre-treating solution can be modified to have different preferred compositions as shown in following table:
-
components complexing Num. Copper ion Hydroxyl ion agent additive 1 3.5 g/L 5 g/L 57 g/L 15 g/ L 2 5.7 g/L 9.1 g/L 27.3 g/L 2 g/ L 3 3.2 g/L 17.3 g/L 66.9 g/L 5 g/L 4 6.2 g/L 8 g/L 27.9 g/L 1.7 g/L 5 5.4 g/L 30 g/L 65 g/L 14.7 g/L 6 6.4 g/L 8.6 g/L 30.9 g/L 1 g/L 7 5.9 g/L 7.7 g/L 26.4 g/L 1.8 g/L 8 13.7 g/L 22.3 g/L 67.8 g/L 3.3 g/L 9 14.6 g/L 25.8 g/L 45.3 g/L 3.2 g/ L 10 15.1 g/L 27.4 g/L 32.4 g/L 5 g/L 11 7.2 g/L 7.9 g/L 21.6 g/L 4.1 g/L 12 17.4 g/L 19.5 g/L 12.7 g/L 3.8 g/ L 13 7.1 g/L 8.5 g/L 33 g/L 3 g/ L 14 22.2 g/L 7.3 g/L 25 g/L 5 g/ L 15 21.6 g/L 17.9 g/L 53 g/L 2.4 g/L 16 24.3 g/L 24.7 g/L 55 g/L 3.5 g/L 17 6.4 g/L 9 g/L 25.8 g/L 2.3 g/L 18 23.8 g/L 6.8 g/L 45 g/L 4.8 g/L 19 25 g/L 19.3 g/L 14.2 g/L 9.7 g/ L 20 7.3 g/L 8.7 g/L 24.9 g/L 2.1 g/ L 21 8.4 g/L 5.5 g/L 66.9 g/L 13.2 g/ L 22 24.1 g/L 6.2 g/L 15.8 g/L 1.7 g/L 23 21. g/L 7.9 g/L 32.3 g/L 11.3 g/L 24 24.8 g/L 9.1 g/L 25 g/L 12.7 g/L - Compositions of the pre-treating solution in serial number of 2, 4, 6, 7, 11, 13, 17 and 20 in the table are mostly preferred.
- With reference to
FIG. 1 , a pre-treating operation to the zinc alloy is shown and is adapted to form a first copper coating layer on a prepared workpiece made of the zinc alloy by using the pre-treating solution in the present invention. The pre-treating operation comprises steps of: - (a). Degreasing:
- The prepared workpiece is degreased with a degreasing agent to remove oil and dirt from its surface.
- (b). Washing:
- The prepared workpiece is washed to remove the degreasing agent and to keep the surface clean.
- (c) Copper Electroplating:
- The workpiece is dipped into the pre-treating solution with auxiliary electrodes and electroplated to obtain a copper coating layer (the first copper coating layer) thereon by applying a fixed current from an additional power supplier.
- (d) Drying:
- After electroplating, residual solution is removed from the surface of the workpiece to make the surface dry rapidly.
- Moreover, a washing step is added into the pre-treating method after the (c) step of copper electroplating.
- Wherein, the surface temperature of the workpiece in (c) step of copper electroplating is about 10 to 90° C.
- Wherein, the fixed current provided by the additional power supplier has a range from 0.002 to 0.02 ampere per square decimeter.
- Wherein, the auxiliary electrodes are made of material selected from the group comprising titanium core coated with platinum, titanium, platinum, graphite and stainless steel.
- With further reference to
FIG. 1 , a preferred embodiment of a pre-treating operation is shown. Before copper electroplating, the workpiece is prepared (10), degreased (11) and washed (12) to make its surface clean. Then, the workpiece, auxiliary electrodes, and the pre-treating solution are inputted into a tank to carry out electroplating (13) with mechanically stir. By applying a fixed current from an additional power supplier, the copper ions in the pre-treating solution obtain electrons to reduce and deposit on the surface of the workpiece so that the workpiece obtains a uniform copper coating layer, i.e. the first copper coating layer. After copper electroplating, the workpiece is washed (14) again and dried (15) to obtain the final product. The workpiece with the first copper coating layer is further treated with a conventional electroplating process to form a second copper coating layer on the first copper coating layer to obtain the final product. Lastly, the workpiece is further coated with an anti-corrosion metal layer to have excellent anti-corrosion and anti-wearing efficiency and varnish appearance. - With reference to
FIG. 2 , the substrate (20) of the zinc alloy is coated with a uniform first copper layer (21) after inputting the substrate (20), the auxiliary electrodes and the pre-treating solution into the tank and carrying out electroplating with mechanically stir by applying a fixed current from the additional power supplier. Thereby, the surface of the zinc alloy substrate (20) becomes brownish in appearance. - With reference to
FIG. 3 , the zinc alloy having the first copper layer (21) is further treated with conventional electroplating by use of market-available copper sulfate solution to form a second copper layer (22) for thickening. - Lastly, the zinc alloy is further treated with an anti-corrosion electroplating to perform a nickel coating (not shown) thereon so that the surface of the zinc alloy is corrosion-resistant and wearing-resistant and has a varnish appearance.
- The cyanide-free pre-treating solution for zinc alloy surface contains an aqua solution added with copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid and hypophosphite acid.
- Wherein, the copper ions are obtained from copper chloride, copper sulfate, copper pyrophosphate or hydrates of foregoing mentioned salts.
- Wherein, concentration of the copper ion is 3 to 50 g/L.
- Wherein, the complexing agent is selected from potassium sodium tartrate, potassium tartrate, sodium tartrate, tartaric acid, and dissolvable salts derivative from tartaric acid.
- Wherein, concentration of the complexing agent is 10 to 150 g/L.
- Wherein, concentration of the additive is 1 to 50 g/L.
- Wherein the hydroxyl ions are obtained from sodium hydroxide, potassium hydroxide, ammonium hydroxide or dissolvable salts of alkaline.
- Wherein, concentration of the hydroxyl ion is 5 to 30 g/L.
- According to above description, the cyanide-free pre-treating solution for zinc alloy surface in accordance with the present invention and its operational method has the following advantages:
- 1. The conventional electroless method is troublesome in pre-treatment. By using the pre-treating solution with copper ions to carry the pre-treatment out, the following nickel layer can be efficiently applied onto the copper layer so that the active zinc alloy surface is completely treated with rapidly and simply two-step electroplating procedures.
- 2. The pre-treating solution in the present invention is alkaline in particular and contains no toxic cyanide, hydrofluoric acid (HF) and chromium trioxide (CrO3) so that it is safe to human being and environment and causes no pollution during electroplating procedures.
- Although the invention has been explained in relation to its preferred embodiment, it is to be understood that many other possible modifications and variations can be made without departing from the spirit and scope of the invention as hereinafter claimed.
Claims (15)
1. A cyanide-free pre-treating solution for zinc alloy surface, the pre-treating solution comprising an aqua solution added with copper ions, hydroxyl ions, a complexing agent and an additive, wherein the additive is selected from the group consisting of sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid or hypophosphite acid.
2. The pre-treating solution as claimed in claim 1 , wherein the additive is 1 to 50 g/L in concentration.
3. The pre-treating solution as claimed in claim 1 , wherein the hydroxyl ions are obtained from the group consisting of sodium hydroxide, potassium hydroxide, ammonium hydroxide and dissolvable salts of alkaline.
4. The pre-treating solution as claimed in claim 1 , wherein the hydroxyl ions are 5 to 30 g/L in concentration.
5. The pre-treating solution as claimed in claim 1 , wherein the complexing agent is selected from the group consisting of potassium sodium tartrate, potassium tartrate, sodium tartrate, tartaric acid, and dissolvable salts derivative from tartaric acid.
6. The pre-treating solution as claimed in claim 5 , wherein the complexing agent is 10 to 150 g/L in concentration.
7. The pre-treating solution as claimed in claim 1 , wherein the copper ions are obtained from the group consisting of copper chloride, copper sulfate, copper pyrophosphate and hydrates of foregoing motioned salts.
8. The pre-treating solution as claimed in claim 7 , wherein the copper ions are 3 to 50 g/L in concentration.
9. A pre-treating method for zinc alloy surface comprising steps of:
(a) degreasing: a prepared workpiece made of zinc alloy is degreased with a degreasing agent to remove oil and dirt from surface of the prepared workpiece;
(b) washing: the prepared workpiece is washed to remove the degreasing agent and to keep the surface of the prepared workpiece clean;
(c) copper electroplating: the prepared workpiece is dipped into the pre-treating solution with auxiliary electrodes and electroplated to obtain a copper coating layer by applying a fixed current from an additional power supplier; and
(d) drying: the pre-treating solution residual on the prepared workpiece is removed from the surface of the workpiece to make the surface dry rapidly.
10. The pre-treating method as claimed in claim 9 further comprising a washing step after (c) step of copper electroplating.
11. The pre-treating method as claimed in claim 9 , wherein the fixed current provided by the additional power supplier has a range from 0.002 to 0.02 ampere per square decimeter.
12. The pre-treating method as claimed in claim 9 , wherein the auxiliary electrodes are made of material selected from the group comprising titanium core coated with platinum, titanium, platinum, graphite and stainless steel.
13. The pre-treating method as claimed in claim 9 , wherein surface temperature of the prepared workpiece in (c) step of copper electroplating is 10 to 90° C.
14. The pre-treating method as claimed in claim 9 , wherein the workpiece is further treated with another copper electroplating process and a nickel coating process after the step of drying.
15. The pre-treating method as claimed in claim 10 , wherein, wherein the pre-treating solution comprises an aqua solution added with copper ions, hydroxyl ions, a complexing agent and an additive;
wherein the additive is selected from the group consisting of sodium phosphate, sodium hypophosphite, phosphoric acid and dissolvable salts derivative from phosphoric acid or hypophosphite acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/646,976 US20080156652A1 (en) | 2006-12-28 | 2006-12-28 | Cyanide-free pre-treating solution for electroplating copper coating layer on zinc alloy surface and a pre-treating method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/646,976 US20080156652A1 (en) | 2006-12-28 | 2006-12-28 | Cyanide-free pre-treating solution for electroplating copper coating layer on zinc alloy surface and a pre-treating method thereof |
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| US20080156652A1 true US20080156652A1 (en) | 2008-07-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/646,976 Abandoned US20080156652A1 (en) | 2006-12-28 | 2006-12-28 | Cyanide-free pre-treating solution for electroplating copper coating layer on zinc alloy surface and a pre-treating method thereof |
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| US (1) | US20080156652A1 (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US20080156653A1 (en) * | 2006-12-28 | 2008-07-03 | Chang Gung University | Cyanide-free pre-treating solution for electroplating copper coating layer on magnesium alloy surface and a pre-treating method thereof |
| US20100084278A1 (en) * | 2008-10-02 | 2010-04-08 | Rowan Anthony J | Novel Cyanide-Free Electroplating Process for Zinc and Zinc Alloy Die-Cast Components |
| US20120217166A1 (en) * | 2009-09-11 | 2012-08-30 | Umicore Galvanotechnik Gmbh | Process for the electrolytic copper plating of zinc diecasting having a reduced tendency to blister formation |
| CN105671600A (en) * | 2016-03-16 | 2016-06-15 | 武汉奥邦表面技术有限公司 | Cyanogen-free alkaline copper electroplating solution |
| CN107435158A (en) * | 2016-05-30 | 2017-12-05 | 建业(惠州)电路版有限公司 | Circuit board electroplating production line capable of plating copper and tin and electroplating method |
| CN114231891A (en) * | 2021-11-23 | 2022-03-25 | 煤炭科学研究总院 | Surface treatment process for coal mine machinery |
| CN114657611A (en) * | 2022-04-20 | 2022-06-24 | 佛山市诺诚科技有限公司 | Alkaline copper electroplating solution and electroplating method thereof |
| CN115881880A (en) * | 2021-08-27 | 2023-03-31 | 北京理工大学 | Method for preparing metal nanocrystalline modified zinc metal negative electrode and application thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US20080156653A1 (en) * | 2006-12-28 | 2008-07-03 | Chang Gung University | Cyanide-free pre-treating solution for electroplating copper coating layer on magnesium alloy surface and a pre-treating method thereof |
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| CN115881880A (en) * | 2021-08-27 | 2023-03-31 | 北京理工大学 | Method for preparing metal nanocrystalline modified zinc metal negative electrode and application thereof |
| CN114231891A (en) * | 2021-11-23 | 2022-03-25 | 煤炭科学研究总院 | Surface treatment process for coal mine machinery |
| CN114657611A (en) * | 2022-04-20 | 2022-06-24 | 佛山市诺诚科技有限公司 | Alkaline copper electroplating solution and electroplating method thereof |
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