US20140079883A1 - Device housing and method for making the device housing - Google Patents
Device housing and method for making the device housing Download PDFInfo
- Publication number
- US20140079883A1 US20140079883A1 US14/085,807 US201314085807A US2014079883A1 US 20140079883 A1 US20140079883 A1 US 20140079883A1 US 201314085807 A US201314085807 A US 201314085807A US 2014079883 A1 US2014079883 A1 US 2014079883A1
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- Prior art keywords
- water solution
- concentration
- base paint
- layer
- paint layer
- 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.)
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Links
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000010410 layer Substances 0.000 claims abstract description 71
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 51
- 239000003973 paint Substances 0.000 claims abstract description 32
- 238000005507 spraying Methods 0.000 claims abstract description 28
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 23
- 229910052709 silver Inorganic materials 0.000 claims abstract description 23
- 239000004332 silver Substances 0.000 claims abstract description 23
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 21
- 239000000758 substrate Substances 0.000 claims abstract description 21
- 230000001235 sensitizing effect Effects 0.000 claims abstract description 18
- 230000003213 activating effect Effects 0.000 claims abstract description 14
- 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 abstract description 14
- 229940074439 potassium sodium tartrate Drugs 0.000 claims abstract description 14
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims abstract description 14
- 235000011006 sodium potassium tartrate Nutrition 0.000 claims abstract description 14
- 239000011241 protective layer Substances 0.000 claims abstract description 11
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims abstract description 7
- 235000011114 ammonium hydroxide Nutrition 0.000 claims abstract description 7
- 229910001961 silver nitrate Inorganic materials 0.000 claims abstract description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 20
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims description 6
- 235000011150 stannous chloride Nutrition 0.000 claims description 6
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 claims description 6
- 238000007598 dipping method Methods 0.000 claims description 5
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 claims description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229910052755 nonmetal Inorganic materials 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- 229910000838 Al alloy Inorganic materials 0.000 claims description 3
- 229910000861 Mg alloy Inorganic materials 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 230000004913 activation Effects 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- 206010070834 Sensitisation Diseases 0.000 description 6
- 230000008313 sensitization Effects 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 238000004381 surface treatment Methods 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- FZUBLAIFQOTUPQ-UHFFFAOYSA-F [OH-].[Sn+4].[Sn+4].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-] Chemical compound [OH-].[Sn+4].[Sn+4].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-] FZUBLAIFQOTUPQ-UHFFFAOYSA-F 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/50—Multilayers
- B05D7/56—Three layers or more
-
- 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
- C23C28/30—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
-
- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04M—TELEPHONIC COMMUNICATION
- H04M1/00—Substation equipment, e.g. for use by subscribers
- H04M1/02—Constructional features of telephone sets
- H04M1/0202—Portable telephone sets, e.g. cordless phones, mobile phones or bar type handsets
- H04M1/0279—Improving the user comfort or ergonomics
- H04M1/0283—Improving the user comfort or ergonomics for providing a decorative aspect, e.g. customization of casings, exchangeable faceplate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
- Y10T428/1393—Multilayer [continuous layer]
Definitions
- the present disclosure relates to device housing and a method for making the device housing.
- Housings of electronic devices are commonly decorated with decorative layers formed by surface treatments.
- the surface treatments may be anodizing, electrophoresis, and painting.
- the decorative layers formed by the mentioned surface treatments are not always aesthetically pleasing.
- FIGURE The components in the FIGURE are not necessarily drawn to scale, the emphasis instead being placed upon clearly illustrating the principles of the disclosure.
- the FIGURE is a cross-sectional view of an exemplary embodiment of a device housing.
- the device housing 100 includes a substrate 10 , a base paint layer 20 directly formed on the substrate 10 .
- a sensitization layer 21 directly formed on the base pain layer 20 an activation layer 23 directly formed on the sensitization layer 21 , a silver layer 30 directly formed on the activation layer 23 , and a protective layer 40 directly formed on the silver layer 30 .
- the substrate 10 may be made of metal or non-metal.
- the metal may be aluminum, aluminum alloy, magnesium, or magnesium alloy, for example.
- the non-metal may be plastic, for example.
- the base paint layer 20 contains mainly acrylic acid epoxy resin.
- the sensitization layer 21 is a thin gel layer containing hydroxide di-tin chloride (Sn 2 (OH) 3 Cl).
- Sn 2 (OH) 3 Cl has reducibility.
- the activation layer 23 contains palladium (Pd) ions.
- the activation layer 23 is evenly dispersed on the sensitization layer 21 .
- the protective layer 40 is a transparent or translucent resin layer and is for protecting the silver layer 30 from being scratched.
- a method for making the device housing 100 may include the following steps.
- the substrate 10 is provided and surface treated.
- the surface treatments for the substrate 10 may be degreasing first and then polishing.
- the base paint layer 20 is sprayed on the substrate 10 .
- the paint or coating used for forming the base paint layer 20 may contain mainly acrylic acid epoxy resin.
- the spraying pressure of the paint or coating for the base paint layer 20 is about 1200 Pa.
- the spraying of the base paint layer 20 lasts for about 2.4 seconds.
- the distance between the substrate 10 and the spray gun (not shown) for spraying the base paint layer 20 is about 20 mm.
- the base paint layer 20 smoothens the substrate 10 .
- the substrate 10 having the base paint layer 20 is baked in an oven (not shown) having an internal temperature of about 88° C. for about 30 minutes.
- the base paint layer 20 is sensitizing treated to form the sensitization layer 21 .
- the sensitizing treatment is carried out by spraying sensitizing water solution to the base paint layer 20 .
- the sensitizing water solution contains hydrochloric acid having a concentration of about 250 g/L to about 400 g/L, tin dichloride having a concentration of about 50 g/L to about 100 g/L, and potassium sodium tartrate having a concentration of about 80 g/L to about 160 g/L.
- the components contained in the sensitizing water solution react to generate the Sn 2 (OH) 3 Cl gel.
- the potassium sodium tartrate acts as a complexant to prevent the bivalent tin of the tin dichloride from oxidizing to tetravalent tin.
- the base paint layer 20 is activating treated to form the activation layer 23 .
- the activating treatment is carried out by dipping the base paint layer 20 having the sensitization layer 21 in an activating water solution for about 5 seconds to about 20 seconds.
- the activating water solution contains hydrochloric acid having a concentration of about 20 g/L to about 50 g/L, and palladium chloride having a concentration of about 0.1 g/L to about 0.5 g/L.
- the Pd ions contained in the activation layer 23 act as a catalyst which accelerate the subsequent silver mirror reaction.
- the substrate 10 having the activation layer 23 is washed and then baked in the oven (not shown) having an internal temperature of about 88° C. for about 30 minutes.
- the silver layer 30 is formed on the activation layer 23 .
- a first water solution and a second water solution are provided.
- the first water solution contains silver nitrate having a concentration of about 20 g/L to about 40 g/L, and ammonia water having a concentration of about 30 g/L to about 50 g/L.
- the second water solution contains potassium sodium tartrate having a concentration of about 80 g/L to about 100 g/L, and sodium hydroxide having a concentration of about 10 g/L to about 20 g/L.
- the first water solution and the second water solution are heated from about 90° C. to about 110° C. and then simultaneously sprayed to the activation layer 23 .
- the spraying process may last for about 10 seconds to about 20 seconds.
- the spraying pressure of the first and second water solution is about 1000 Pa to about 1500 Pa.
- the potassium sodium tartrate of the second water solution acts as a reductant during the silver mirror reaction.
- the substrate 10 having the silver layer 30 is washed and then baked in an oven (not shown) having an internal temperature of about 60° C. for about 30 minutes.
- the protective layer 40 is sprayed on the silver layer 30 using transparent or translucent coating, such as acrylic acid epoxy resin coating.
- the spraying pressure of the coating for the protective layer 40 is about 1200 Pa.
- the spraying of the protective layer 40 lasts for about 2.4 seconds.
- the distance between the substrate 10 and the spray gun (not shown) for spraying the protective layer 40 is about 20 mm.
- the substrate 10 having the protective layer 40 is then baked in the oven (not shown) having an internal temperature of about 88° C. for about 30 minutes to finish the device housing 100 .
- the substrate 10 was made of magnesium alloy.
- Sensitizing treatment the hydrochloric acid of the sensitizing water solution had a concentration of 250 g/L, tin dichloride had a concentration of 55 g/L, and potassium sodium tartrate had a concentration of 80 g/L.
- the palladium chloride had a concentration of 0.15 g/L, and the hydrochloric acid had a concentration of 20 g/L; the dipping process lasted for 5 seconds.
- Spraying the silver layer 30 in the first water solution, the silver nitrate had a concentration of 25 g/L, and the ammonia water had a concentration of 35 g/L; in the second water solution, the potassium sodium tartrate had a concentration of 85 g/L, and the sodium hydroxide had a concentration of 12 g/L; the first and the second water solution was heated to 100° C.; the spraying pressure of the first and the second water solution was 1100 Pa; the spraying process lasted for 15 seconds; the silver layer 30 was baked at an internal oven temperature of about 60° C. for about 30 minutes.
- the substrate 10 was made of aluminum alloy.
- Sensitizing treatment the hydrochloric acid of the sensitizing water solution had a concentration of 300 g/L, tin dichloride had a concentration of 80 g/L, and potassium sodium tartrate had a concentration of 120 g/L.
- the palladium chloride had a concentration of 0.30 g/L, and the hydrochloric acid had a concentration of 35 g/L; the dipping process lasted for 8 seconds.
- Spraying the silver layer 30 in the first water solution, the silver nitrate had a concentration of 30 g/L, and the ammonia water had a concentration of 40 g/L; in the second water solution, the potassium sodium tartrate had a concentration of 95 g/L, and the sodium hydroxide had a concentration of 10 g/L; the first and the second water solution was heated to 95° C.; the spraying pressure of the first and the second water solution was 1200 Pa; the spraying process lasted for 10 seconds; the silver layer 30 was baked at an internal oven temperature of about 60° C. for about 30 minutes.
- the substrate 10 was made of plastic.
- Sensitizing treatment the hydrochloric acid of the sensitizing water solution had a concentration of 400 g/L, tin dichloride had a concentration of 100 g/L, and potassium sodium tartrate had a concentration of 160 g/L.
- the palladium chloride had a concentration of 0.40 g/L, and the hydrochloric acid had a concentration of 50 g/L; the dipping process lasted for 10 seconds.
- Spraying the silver layer 30 in the first water solution, the silver nitrate had a concentration of 35 g/L, and the ammonia water had a concentration of 45 g/L; in the second water solution, the potassium sodium tartrate had a concentration of 90 g/L, and the sodium hydroxide had a concentration of 15 g/L; the first and the second water solution was heated to 105° C.; the spraying pressure of the first and the second water solution was 1400 Pa; the spraying process lasted for 20 seconds; the silver layer 30 was baked at an internal oven temperature of about 60° C. for about 30 minutes.
- the device housing 100 of the exemplary embodiments define a silver layer 30 to provide the device housing 100 a silvery white and metallic appearance. Furthermore, the silver layer 30 can highly reflect light, which renders the device housing 100 high gloss.
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- Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemically Coating (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
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- Chemical Treatment Of Metals (AREA)
Abstract
A method for making a device housing includes the steps of: providing a substrate; forming a base paint layer on the substrate by spraying; sensitizing a surface of the base paint layer; activating the surface of the base paint layer; providing a first water solution and a second water solution, the first water solution containing silver nitrate and ammonia water, the second water solution containing potassium sodium tartrate and sodium hydroxide; forming a silver layer on the sensitized and activated surface of the base paint layer by simultaneously spraying the first water solution and the second water solution on the sensitized and activated surface of the base paint layer; and forming a protective layer on the silver layer.
Description
- This application is a divisional application of U.S. Ser. No. 13/593,621, filed Aug. 24, 2012, the contents of which are hereby incorporated by reference. The patent application Ser. No. 13/593,621 in turn claims the benefit of priority under 35 USC 119 from Chinese Patent Application 201110359319.X, filed on Nov. 14, 2011.
- 1. Technical Field
- The present disclosure relates to device housing and a method for making the device housing.
- 2. Description of Related Art
- Housings of electronic devices, such as mobile phones, are commonly decorated with decorative layers formed by surface treatments. The surface treatments may be anodizing, electrophoresis, and painting. However, the decorative layers formed by the mentioned surface treatments are not always aesthetically pleasing.
- Therefore, there is room for improvement within the art.
- Many aspects of the disclosure can be better understood with reference to the following FIGURE. The components in the FIGURE are not necessarily drawn to scale, the emphasis instead being placed upon clearly illustrating the principles of the disclosure.
- The FIGURE is a cross-sectional view of an exemplary embodiment of a device housing.
- Referring to the FIGURE, a device housing 100 according to an exemplary embodiment is shown. The
device housing 100 includes asubstrate 10, abase paint layer 20 directly formed on thesubstrate 10. Asensitization layer 21 directly formed on thebase pain layer 20, anactivation layer 23 directly formed on thesensitization layer 21, a silver layer 30 directly formed on theactivation layer 23, and aprotective layer 40 directly formed on the silver layer 30. - The
substrate 10 may be made of metal or non-metal. The metal may be aluminum, aluminum alloy, magnesium, or magnesium alloy, for example. The non-metal may be plastic, for example. - The
base paint layer 20 contains mainly acrylic acid epoxy resin. - The
sensitization layer 21 is a thin gel layer containing hydroxide di-tin chloride (Sn2(OH)3Cl). The Sn2(OH)3Cl has reducibility. - The
activation layer 23 contains palladium (Pd) ions. Theactivation layer 23 is evenly dispersed on thesensitization layer 21. - The
protective layer 40 is a transparent or translucent resin layer and is for protecting the silver layer 30 from being scratched. - A method for making the
device housing 100 may include the following steps. - The
substrate 10 is provided and surface treated. The surface treatments for thesubstrate 10 may be degreasing first and then polishing. - The
base paint layer 20 is sprayed on thesubstrate 10. The paint or coating used for forming thebase paint layer 20 may contain mainly acrylic acid epoxy resin. The spraying pressure of the paint or coating for thebase paint layer 20 is about 1200 Pa. The spraying of thebase paint layer 20 lasts for about 2.4 seconds. During the spraying, the distance between thesubstrate 10 and the spray gun (not shown) for spraying thebase paint layer 20 is about 20 mm. Thebase paint layer 20 smoothens thesubstrate 10. - The
substrate 10 having thebase paint layer 20 is baked in an oven (not shown) having an internal temperature of about 88° C. for about 30 minutes. - The
base paint layer 20 is sensitizing treated to form thesensitization layer 21. The sensitizing treatment is carried out by spraying sensitizing water solution to thebase paint layer 20. The sensitizing water solution contains hydrochloric acid having a concentration of about 250 g/L to about 400 g/L, tin dichloride having a concentration of about 50 g/L to about 100 g/L, and potassium sodium tartrate having a concentration of about 80 g/L to about 160 g/L. The components contained in the sensitizing water solution react to generate the Sn2(OH)3Cl gel. In the sensitizing water solution, the potassium sodium tartrate acts as a complexant to prevent the bivalent tin of the tin dichloride from oxidizing to tetravalent tin. - The
base paint layer 20 is activating treated to form theactivation layer 23. The activating treatment is carried out by dipping thebase paint layer 20 having thesensitization layer 21 in an activating water solution for about 5 seconds to about 20 seconds. The activating water solution contains hydrochloric acid having a concentration of about 20 g/L to about 50 g/L, and palladium chloride having a concentration of about 0.1 g/L to about 0.5 g/L. The Pd ions contained in theactivation layer 23 act as a catalyst which accelerate the subsequent silver mirror reaction. - The
substrate 10 having theactivation layer 23 is washed and then baked in the oven (not shown) having an internal temperature of about 88° C. for about 30 minutes. - The silver layer 30 is formed on the
activation layer 23. A first water solution and a second water solution are provided. The first water solution contains silver nitrate having a concentration of about 20 g/L to about 40 g/L, and ammonia water having a concentration of about 30 g/L to about 50 g/L. The second water solution contains potassium sodium tartrate having a concentration of about 80 g/L to about 100 g/L, and sodium hydroxide having a concentration of about 10 g/L to about 20 g/L. The first water solution and the second water solution are heated from about 90° C. to about 110° C. and then simultaneously sprayed to theactivation layer 23. Then a silver mirror reaction is generated between the components of the first and second water solutions, thereby forming the silver layer 30 on theactivation layer 23. The spraying process may last for about 10 seconds to about 20 seconds. The spraying pressure of the first and second water solution is about 1000 Pa to about 1500 Pa. The potassium sodium tartrate of the second water solution acts as a reductant during the silver mirror reaction. - The
substrate 10 having the silver layer 30 is washed and then baked in an oven (not shown) having an internal temperature of about 60° C. for about 30 minutes. - The
protective layer 40 is sprayed on the silver layer 30 using transparent or translucent coating, such as acrylic acid epoxy resin coating. The spraying pressure of the coating for theprotective layer 40 is about 1200 Pa. The spraying of theprotective layer 40 lasts for about 2.4 seconds. During the spraying, the distance between thesubstrate 10 and the spray gun (not shown) for spraying theprotective layer 40 is about 20 mm. Thesubstrate 10 having theprotective layer 40 is then baked in the oven (not shown) having an internal temperature of about 88° C. for about 30 minutes to finish thedevice housing 100. - Specific examples of making the
device housing 100 are described below. The forming and baking of thebase paint layer 20 and theprotective layer 40 in these specific examples may be substantially the same as described above so it is not described here again The specific examples mainly emphasize the specific concentrations of the water solutions and different process parameters for the sensitizing treatment, the activating treatment, and the spraying of the silver layer 30. - The
substrate 10 was made of magnesium alloy. - Sensitizing treatment: the hydrochloric acid of the sensitizing water solution had a concentration of 250 g/L, tin dichloride had a concentration of 55 g/L, and potassium sodium tartrate had a concentration of 80 g/L.
- Activating treatment: in the activating water solution, the palladium chloride had a concentration of 0.15 g/L, and the hydrochloric acid had a concentration of 20 g/L; the dipping process lasted for 5 seconds.
- Spraying the silver layer 30: in the first water solution, the silver nitrate had a concentration of 25 g/L, and the ammonia water had a concentration of 35 g/L; in the second water solution, the potassium sodium tartrate had a concentration of 85 g/L, and the sodium hydroxide had a concentration of 12 g/L; the first and the second water solution was heated to 100° C.; the spraying pressure of the first and the second water solution was 1100 Pa; the spraying process lasted for 15 seconds; the silver layer 30 was baked at an internal oven temperature of about 60° C. for about 30 minutes.
- The
substrate 10 was made of aluminum alloy. - Sensitizing treatment: the hydrochloric acid of the sensitizing water solution had a concentration of 300 g/L, tin dichloride had a concentration of 80 g/L, and potassium sodium tartrate had a concentration of 120 g/L.
- Activating treatment: in the activated water solution, the palladium chloride had a concentration of 0.30 g/L, and the hydrochloric acid had a concentration of 35 g/L; the dipping process lasted for 8 seconds.
- Spraying the silver layer 30: in the first water solution, the silver nitrate had a concentration of 30 g/L, and the ammonia water had a concentration of 40 g/L; in the second water solution, the potassium sodium tartrate had a concentration of 95 g/L, and the sodium hydroxide had a concentration of 10 g/L; the first and the second water solution was heated to 95° C.; the spraying pressure of the first and the second water solution was 1200 Pa; the spraying process lasted for 10 seconds; the silver layer 30 was baked at an internal oven temperature of about 60° C. for about 30 minutes.
- The
substrate 10 was made of plastic. - Sensitizing treatment: the hydrochloric acid of the sensitizing water solution had a concentration of 400 g/L, tin dichloride had a concentration of 100 g/L, and potassium sodium tartrate had a concentration of 160 g/L.
- Activating treatment: in the activated water solution, the palladium chloride had a concentration of 0.40 g/L, and the hydrochloric acid had a concentration of 50 g/L; the dipping process lasted for 10 seconds.
- Spraying the silver layer 30: in the first water solution, the silver nitrate had a concentration of 35 g/L, and the ammonia water had a concentration of 45 g/L; in the second water solution, the potassium sodium tartrate had a concentration of 90 g/L, and the sodium hydroxide had a concentration of 15 g/L; the first and the second water solution was heated to 105° C.; the spraying pressure of the first and the second water solution was 1400 Pa; the spraying process lasted for 20 seconds; the silver layer 30 was baked at an internal oven temperature of about 60° C. for about 30 minutes.
- The
device housing 100 of the exemplary embodiments define a silver layer 30 to provide the device housing 100 a silvery white and metallic appearance. Furthermore, the silver layer 30 can highly reflect light, which renders thedevice housing 100 high gloss. - It is believed that the exemplary embodiment and its advantages will be understood from the foregoing description, and it will be apparent that various changes may be made thereto without departing from the spirit and scope of the disclosure or sacrificing all of its advantages, the examples hereinbefore described merely being preferred or exemplary embodiment of the disclosure.
Claims (9)
1. A method for making a device housing, comprising:
providing a substrate;
forming a base paint layer on the substrate by spraying;
sensitizing a surface of the base paint layer;
activating the surface of the base paint layer;
providing a first water solution and a second water solution, the first water solution containing silver nitrate and ammonia water, the second water solution containing potassium sodium tartrate and sodium hydroxide;
forming a silver layer on the sensitized and activated surface of the base paint layer by simultaneously spraying the first water solution and the second water solution on the sensitized and activated surface of the base paint layer;
forming a protective layer on the silver layer.
2. The method as claimed in claim 1 , wherein the silver nitrate has a concentration of about 20 g/L to about 40 g/L, the ammonia water has a concentration of about 30 g/L to about 50 g/L, the potassium sodium tartrate has a concentration of about 80 g/L to about 100 g/L, and the sodium hydroxide has a concentration of about 10 g/L to about 20 g/L.
3. The method as claimed in claim 2 , wherein the first and second water solutions have a temperature of about 90° C. to about 110° C., and have a spraying pressure of about 1000 Pa to about 1500 Pa.
4. The method as claimed in claim 1 , wherein sensitizing the surface of the base paint layer is carried out by spraying sensitizing water solution to the base paint layer, the sensitizing water solution contains hydrochloric acid having a concentration of about 250 g/L to about 400 g/L, tin dichloride having a concentration of about 50 g/L to about 100 g/L, and potassium sodium tartrate having a concentration of about 80 g/L to about 160 g/L.
5. The method as claimed in claim 1 , wherein activating the surface of the base paint layer is carried out by dipping the base paint layer in an activating water solution for about 5 seconds to about 20 seconds, the activating water solution contains hydrochloric acid having a concentration of about 20 g/L to about 50 g/L, and palladium chloride having a concentration of about 0.1 g/L to about 0.5 g/L.
6. The method as claimed in claim 1 , wherein the base paint layer comprises acrylic acid epoxy resin.
7. The method as claimed in claim 1 , wherein the protective layer is a paint layer comprising transparent or translucent resin formed by spraying.
8. The method as claimed in claim 1 , wherein the substrate is made of metal or non-metal.
9. The method as claimed in claim 8 , wherein the metal is aluminum, aluminum alloy, magnesium, or magnesium alloy, the non-metal is plastic.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14/085,807 US20140079883A1 (en) | 2011-11-14 | 2013-11-21 | Device housing and method for making the device housing |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110359319XA CN103108507A (en) | 2011-11-14 | 2011-11-14 | Shell body of electronic device and manufacturing method thereof |
| CN201110359319.X | 2011-11-14 | ||
| US13/593,621 US8617682B2 (en) | 2011-11-14 | 2012-08-24 | Device housing and method for making the device housing |
| US14/085,807 US20140079883A1 (en) | 2011-11-14 | 2013-11-21 | Device housing and method for making the device housing |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/593,621 Division US8617682B2 (en) | 2011-11-14 | 2012-08-24 | Device housing and method for making the device housing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20140079883A1 true US20140079883A1 (en) | 2014-03-20 |
Family
ID=48280908
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/593,621 Expired - Fee Related US8617682B2 (en) | 2011-11-14 | 2012-08-24 | Device housing and method for making the device housing |
| US14/085,807 Abandoned US20140079883A1 (en) | 2011-11-14 | 2013-11-21 | Device housing and method for making the device housing |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/593,621 Expired - Fee Related US8617682B2 (en) | 2011-11-14 | 2012-08-24 | Device housing and method for making the device housing |
Country Status (3)
| Country | Link |
|---|---|
| US (2) | US8617682B2 (en) |
| CN (1) | CN103108507A (en) |
| TW (1) | TW201319309A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104320507A (en) * | 2014-10-22 | 2015-01-28 | 深圳市杰美特科技股份有限公司 | Non-flip visible protective jacket and manufacture method thereof |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103108507A (en) * | 2011-11-14 | 2013-05-15 | 深圳富泰宏精密工业有限公司 | Shell body of electronic device and manufacturing method thereof |
| CN104411136B (en) * | 2014-10-28 | 2018-07-06 | 广东欧珀移动通信有限公司 | The manufacturing method of mobile terminal shell, mobile terminal and mobile terminal shell |
| CN107548255A (en) * | 2017-08-07 | 2018-01-05 | 维沃移动通信有限公司 | A kind of terminal shell and preparation method thereof |
| CN113498285B (en) * | 2020-04-08 | 2023-02-17 | Oppo广东移动通信有限公司 | Housing assembly, manufacturing method thereof, and electronic device |
| CN111763930B (en) * | 2020-07-14 | 2022-04-19 | 赤壁市聚茂新材料科技有限公司 | Non-palladium activated copper plating process and sensitizer and activator thereof |
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| US4042730A (en) * | 1976-03-29 | 1977-08-16 | Bell Telephone Laboratories, Incorporated | Process for electroless plating using separate sensitization and activation steps |
| US20020094433A1 (en) * | 2001-01-17 | 2002-07-18 | Kevin Hug | Electrically conductive foam and method of preparation thereof |
| US6979478B1 (en) * | 2002-08-01 | 2005-12-27 | Hilemn, Llc | Paint for silver film protection and method |
| US20060035018A1 (en) * | 2002-11-01 | 2006-02-16 | Advance Company, Ltd. | Method for forming a thin film silver mirror and method for forming coated film comprising thin silver mirror film |
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| CN101096769A (en) * | 2006-06-26 | 2008-01-02 | 比亚迪股份有限公司 | A method of electroplating |
| CN100494489C (en) * | 2006-10-11 | 2009-06-03 | 方宏亮 | Nano mirror spraying |
| CN101431873A (en) * | 2007-11-09 | 2009-05-13 | 深圳富泰宏精密工业有限公司 | Metal case and manufacturing method thereof |
| CN101200350B (en) * | 2007-12-18 | 2012-08-22 | 张家港雅博纳米材料科技有限公司 | Method for processing silver mirror coating |
| CN101765344B (en) * | 2008-12-26 | 2013-01-30 | 比亚迪股份有限公司 | Display case, preparation method thereof, and electronic product including the display case |
| CN101773904B (en) * | 2010-02-09 | 2012-05-02 | 林文友 | Mirror surface nano spraying method |
| CN103108507A (en) * | 2011-11-14 | 2013-05-15 | 深圳富泰宏精密工业有限公司 | Shell body of electronic device and manufacturing method thereof |
-
2011
- 2011-11-14 CN CN201110359319XA patent/CN103108507A/en active Pending
- 2011-11-18 TW TW100142300A patent/TW201319309A/en unknown
-
2012
- 2012-08-24 US US13/593,621 patent/US8617682B2/en not_active Expired - Fee Related
-
2013
- 2013-11-21 US US14/085,807 patent/US20140079883A1/en not_active Abandoned
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4042730A (en) * | 1976-03-29 | 1977-08-16 | Bell Telephone Laboratories, Incorporated | Process for electroless plating using separate sensitization and activation steps |
| US20020094433A1 (en) * | 2001-01-17 | 2002-07-18 | Kevin Hug | Electrically conductive foam and method of preparation thereof |
| US6979478B1 (en) * | 2002-08-01 | 2005-12-27 | Hilemn, Llc | Paint for silver film protection and method |
| US20060035018A1 (en) * | 2002-11-01 | 2006-02-16 | Advance Company, Ltd. | Method for forming a thin film silver mirror and method for forming coated film comprising thin silver mirror film |
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| CN104320507A (en) * | 2014-10-22 | 2015-01-28 | 深圳市杰美特科技股份有限公司 | Non-flip visible protective jacket and manufacture method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| US8617682B2 (en) | 2013-12-31 |
| CN103108507A (en) | 2013-05-15 |
| TW201319309A (en) | 2013-05-16 |
| US20130122224A1 (en) | 2013-05-16 |
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