[0001] The present disclosure relates to a surface treatment method for housings, especially
to an electroplating method for metal housings.
[0002] A typical surface treatment method now for portable electronic devices' housings
is electroplating. Commonly, the housing is electroplated to form a trivalent chromium
coating on its surface to present high gloss appearance and enhance abrasion resistance.
To enhance the bonding between the trivalent chromium coating and the housing, the
housing is electroplated with a nickel coating prior to the forming of the chromium
coating. However, the nickel coating and the whole process of electroplating with
nickel are not environmentally friendly because the nickel or nickel iron contained
in the electrolyte is toxic.
[0003] Therefore, there is room for improvement within the art.
BRIEF DESCRIPTION OF THE DRAWING
[0004] Many aspects of the surface treatment method for housing can be better understood
with reference to Figure 1. The emphasis of Figure 1 is placed upon clearly illustrating
the principles of the surface treatment for housing.
[0005] Figure 1 is a flow chart of an exemplary embodiment of a surface treatment method
for a housing.
DETAILED DESCRIPTION
[0006] Referring to Figure 1, a surface treatment method for a housing may include the steps
S10 to S50.
[0007] In step S10, a metal housing is provided. The metal housing may be made of, e.g.,
stainless steel or copper. The metal housing may be a mobile phone, a digital camera,
a personal digital assistant, or a note book computer's housing. The metal housing
may also be a housing of a container.
[0008] In step S20, the metal housing is pretreated. The pre-treating step may comprise
one or more of the following: degreasing, electrochemical cleaning, and acid treating
the housing.
[0009] The degreasing process may be carried out by dipping the housing in a degreasing
solution for about 5-15 minutes. The mass concentration of the degreasing agent is
about 150-200 grams per liter (g/L). The temperature of the degreasing solution is
about 55-65 °C.
[0010] After the degreasing process, the housing is removed from the degreasing solution
to be electrochemically cleaned. Electrochemical cleaning the housing may be carried
out in a first electrolyte. The first electrolyte may contain a sodium hydroxide component
in a mass concentration of about 100-200 g/L and an activating agent(s) component
in a mass concentration of about 40-80 g/L. The activating agent(s) may be dodecyl
sulfonic acid sodium salt. The temperature of the first electrolyte is about 55-65
°C. The electric current density through the first electrolyte is about 1-5 A/dm
2. Electrochemically cleaning the housing may last for about 4-10 minutes. The electrochemical
cleaning step can further remove lipids adhering to the housing and smudges.
[0011] After the electrochemical cleaning process, the housing is dipped in a sulfuric acid
solution for about 1-5 minutes to remove the residual basic liquid adhering to the
housing's surface. The concentration by volume of the sulfuric acid in the solution
is about 50-80 ml/L. The temperature of the sulfuric acid solution is about 20-30
°C. After the acid treatment, the housing is water washed; in this embodiment the
housing is water washed three times.
[0012] In step S30, the housing is electroplated to form a hexavalent chromium coating on
its surface. Electroplating the housing to form the hexavalent chromium coating may
be carried out in a second electrolyte, with the metalized surface of the housing
being a cathode, and a stannum (Sn) plumbum (Pb) alloy anode being provided and immersed
in the second electrolyte. The second electrolyte may contain a chromium acid (H
2CrO
4) component in a mass concentration of about 240-350 g/L and a sulfuric acid component
in a mass concentration of about 2-4 g/L. The second electrolyte may further contain
additive agent(s), such as fluoride. The additive agent(s) may improve the forming
of the hexavalent chromium coating on the surface of the housing. The mass concentration
of the additive agent(s) in the second electrolyte is about 5-10 g/L. The electric
current density through the second electrolyte is about 10-30 A/dm
2. Electroplating the housing with the hexavalent chromium coating may last for about
1-15 minutes. The hexavalent chromium coating bonds well with the housing because
of having similar properties as copper or stainless steel. After the electroplating,
the housing is bathed in water.
[0013] In step S40, the housing is electroplated to form a trivalent chromium coating on
the hexavalent chromium coating. Electroplating the housing to form the trivalent
chromium coating may be carried out in a third electrolyte, with the metalized surface
of the housing being a cathode, and a iridium (Ir) tantalum (Ta) alloy anode being
provided and immersed in the third electrolyte. The third electrolyte may contain
a chromium sulphate (Cr
2(SO
4)
3) component in a mass concentration of about 240-300 g/L, and a boric acid component
in a mass concentration of about 70-90 g/L. The third electrolyte may further contain
additive agent(s) such as bromide and formate. The mass concentration of the bromide
in the third electrolyte is about 15-20 g/L, and the mass concentration of the formate
is about 70-90 g/L. The mass concentration of the trivalent chromium iron in the third
electrolyte is about 3-10 g/L. The electric current density through the third electrolyte
is about 5-15 A/dm
2. Electroplating the housing with the trivalent chromium coating may last for about
1-15 minutes. The trivalent chromium coating bond well with the hexavalent chromium
coating for the two coatings are all contain the chromium element. The trivalent chromium
coating being formed on the hexavalent chromium coating prevents the problem that
the trivalent chromium coating is tend to split for directly formed on the surface
of the housing.
[0014] After electroplating, the housing is again bathed in water.
[0015] In step S50, the housing is subjected to neutralization treatment. The neutralization
treatment is carried out by dipping the housing in a neutralization solution for about
1-3 minutes to remove any residual electrolyte adhering to the housing. The neutralization
solution includes a sulfuric acid component in a concentration by volume of about
20-50 ml/L, and an oxydol component in a concentration by volume of about 50-100 ml/L.
The temperature of the neutralization solution is about 20-30 °C. After receiving
neutralization treatment, the housing is bathed once more in water.
[0016] The surface treatment method for housing described above forms a hexavalent chromium
coating on the surface of the housing prior to forming the trivalent chromium coating,
which prevents the tendency of the trivalent chromium coating to split when directly
formed on the surface of the housing, and enhances the bonding between the trivalent
chromium and the housing. The two chromium coatings can further enhance the rigidity
of the housing and make the housing present more glossy appearance, thus producing
better protected parts of the housing. Moreover, the two coatings do not contain nickel
and so are more environmentally friendly.
[0017] It is believed that the present 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.
1. A surface treatment method for a housing, comprising:
providing a metal housing and pre-treating it to be cleaned;
electroplating the housing to form a hexavalent chromium coating on a surface of the
housing; and
electroplating the housing to form a trivalent chromium coating on the hexavalent
chromium coating.
2. The surface treatment method as claimed in claim 1, wherein the metal housing is made
of stainless steel or copper.
3. The surface treatment method as claimed in claim 1, wherein electroplating the housing
to form the hexavalent chromium coating is carried out in a second electrolyte containing
a chromium acid component in a mass concentration of about 240-350 g/L and a sulfuric
acid component in a mass concentration of about 2-4 g/L.
4. The surface treatment method as claimed in claim 3, wherein the second electrolyte
further contains fluoride additive agent(s) in a mass concentration of about 5-10
g/L.
5. The surface treatment method as claimed in claim 4, wherein the electric current density
through the second electrolyte is about 10-30 A/dm2, and the electroplating last for about 1-15 minutes.
6. The surface treatment method as claimed in claim 1, wherein electroplating the housing
to form the trivalent chromium coating is carried out in a third electrolyte containing
a chromium sulphate component and a boric acid component, the mass concentration of
the trivalent chromium iron in the third electrolyte is about 3-10 g/L.
7. The surface treatment method as claimed in claim 6, wherein the electric current density
through the third electrolyte is about 5-15 A/dm2, and the electroplating last for about 1-15 minutes.
8. The surface treatment method as claimed in claim 1, wherein the housing is subjected
to neutralization treatment after the electroplating process in a neutralization solution
including a sulfuric acid component and an oxydol component.
9. The surface treatment method as claimed in claim 1, wherein pre-treating the housing
includes degreasing, electrochemical cleaning and acid treating the housing.
10. The surface treatment method as claimed in claim 9, wherein electrochemical cleaning
the housing is carried out in a first electrolyte containing a sodium hydroxide component,
the temperature of the first electrolyte is about 55-65 °C, the electric current density
through the first electrolyte is about 1-5 A/dm2, and the electrochemical cleaning last for about 4-10 minutes.