[0001] This invention relates to a plating method for steel sheet. More particularly, it
relates to an electroplating method of hot-galvanized steel sheet. It also relates
to a plating line in which a steel sheet is continuously subjected to hot-galvanizing
and then electroplating. The resulting plated steel sheet has an electroplated top
coating with excellent covering power and adhesion to the underlying hot-galvanized
coating.
[0002] In the automotive and construction industries, there is always a great demand for
materials having good corrosion resistance and a long life span. In particular, the
corrosion resistance demanded of rust-preventive steel sheets for automobile bodies
has become extreme.
[0003] In order to meet these demands, various new types of electroplated steel sheets have
been proposed, such as steel sheets electroplated with a Zn-Ni, Zn-Fe, or Zn-Mn alloy,
steel sheets hot-dip plated with a Zn-Fe, Zn-Al-Si, or Zn-Al-Mg alloy. Steel sheet
having multiple plated layers in which the top layer is an Fe-rich (Fe ≧ 60%) Fe-Zn
alloy plated coating has also been developed with the intention to improve the coatability
of the plated steel sheet by cationic electrodeposition performed thereon and to increase
the adhesion of the electrodeposited coating in water (see Japanese published Unexamined
Patent Application No. 56-133488).
[0004] Steel sheet with a plurality of layers of plated coating (hereinafter referred to
as multi-layer plated steel sheet) is highly suitable for use in automobiles and as
a construction material not only on account of its coatability but also because of
its excellent press forming characteristics (sliding properties), weldability, and
various other properties.
[0005] The multi-layer electroplating that have been proposed in the prior art include a
Zn-Ni/Fe or Fe-Zn coating (Japanese published Examined Patent Application No. 60-57518),
a Zn-Ni/Zn or Zn-Ni or Zn-Fe/Cr(Cr-oxide) coating (Japanese Published Unexamined Patent
Application No. 60-197893), a Zn-Mn/Zn-Fe coating (Japanese Publised Unexamined Patent
Application No. 58-42787), and a Zn or Zn alloy/minute particle-dispersed Zn or Zn
alloy coating (Japanese Publised Unexamined Patent Application No. 62-230999).
[0006] Recently, it has also been proposed to perform electroplating on an alloyed hot-galvanized
steel sheet (Japanese Publised Unexamined Patent Applications Nos. 56-133488 and 61-253397).
[0007] When forming multi-layer electroplated coating using a single electroplating line,
normally, plating baths for different types of coatings are arranged in series along
the line. Equipment for dip water rinsing and, if necessary, equipment for rinsing
with hot water or with brushes is installed between successive baths. However, no
treatment other than rinsing or scrubbing is performed on the steel sheet as it is
passed from one bath to another.
[0008] Similarly, when a steel sheet is hot-galvanized and then electroplated in a continuous
process, equipment for continuous electroplating is simply connected in series with
equipment for continuous hot-galvanizing, and no special treatments are performed
on the steel sheet as it travels between the two sets of equipment.
[0009] For example, Japanese Published Unexamined Patent Application No. 60-224791 discloses
a continuous plating apparatus in which a pretreatment apparatus, a hot-galvanizing
bath, an alloying furnace, and an electroplating apparatus are connected in series.
A skin-pass rolling mill and, if necessary, a water rinse tank may be disposed between
the hot-galvanizing bath and the electroplating apparatus.
[0010] Japanese Published Unexamined Patent Application No. 62-17200 discloses a continuous
one-sided plating apparatus in which a pretreatment apparatus, a hot-galvanizing bath
for plating one side of a steel sheet, an alloying furnace, a cleaning apparatus for
cleaning the unplated side of the sheet, and an electroplating apparatus are connected
in series.
[0011] In these continuous plating apparatuses, no special chemical treatment is performed
on the hot-dipped coating of the sheet before electroplating.
[0012] However, the present inventors' research has shown that when two different processes,
such as hot-galvanizing and electroplating, are arranged in sequence, the following
problems occur.
(1) If continuous electroplating is performed after hot-galvanizing of a steel sheet,
electroplated coatings such as a Fe or Fe-based alloy (Fe-Zn, etc.), Cr(Cr-oxide),
Ni, and Zn-Ni alloy coatings have poor adhesion to the galvanized coating, and these
coatings tend to readily peel off either while the coated sheet is still flat or after
it has been subjected to working (bending, drawing, etc.).
(2) If a hot-galvanized steel sheet is heated to perform alloying of the galvanized
coating prior to electroplating, the resulting alloyed galvanized coating has microscopic
surface irregularities, i.e., bumps and depressions, which are inherent in an alloyed
galvanized steel sheet (usually called GA steel sheet). The irregularities include
those which are caused by the crystalline form of the Zn-Fe alloy and microscopic
depressions which are formed during alloying. They generally have a size of 3 - 20
micrometers.
[0013] Such microscopic surface irregularities, and particularly the depressions, cannot
be adequately covered by the overlaid electroplated coating. When the electroplated
coating is one such as an Fe coating which is intended to increase the coatability
of the plated steel sheet by cationic electrodeposition, the electroplated coating
cannot adequately perform its intended function.
[0014] The covering power of an electroplated coating with respect to microscopic irregularities
will hereunder be referred to as its microcovering power.
[0015] Thus, it is not possible to achieve a hot-galvanized electroplated steel sheet of
high quality simply by connecting a continuous hot-galvanizing apparatus and a continuous
electroplating apparatus in sequence.
[0016] Accordingly, it is an object of the present invention to provide a plating line for
performing continuous galvanizing and electroplating of steel sheet which can form
an electroplated coating having excellent microcovering power.
[0017] It is another object of the present invention to provide a continuous plating line
of steel sheet in which conventional hot-galvanizing and electroplating equipment
is used.
[0018] It is a further object of the present invention to provide a method for electroplating
a galvanized steel sheet to form an electroplated coating having excellent microcovering
power.
[0019] It is a still further object of the present invention to provide a continuous galvanizing
and electroplating method which can be performed in a single plating line to form
a hot-galvanized electroplated steel sheet of high quality.
[0020] According to the method of the present invention, a hot-galvanized steel sheet is
subjected to post-galvanizing surface treatment prior to electroplating in order to
remove oxide and other surface contaminants (hereinafter collectively referred to
as surface oxide contaminants) and activate the surface of the galvanized coating.
[0021] The post-galvanizing surface treatment employed in the present invention greatly
increases the adhesion and covering power of an electroplated coating. The reasons
for these improvements are not yet clear. However, it is thought that the surface
treatment improves properties by dissolving away aluminum oxide and an Zn-containing
aluminum oxide which are formed on the surface of a galvanized coating of a steel
sheet by the heat applied by hot-galvanizing or alloying and which have poor electrical
conductivity. Furthermore, it can remove Al and other metallic contaminants which
segregates on the surface and which are thought to influence electro-deposition of
an electroplated coating.
[0022] The post-galvanizing surface treatment can be any form of treatment which can remove
surface oxide contaminants which adversely affect the microcovering power of an electroplated
coating. The surface treatment may be carried out by applying a strong alkali solution
or an acid which can dissolve aluminum oxide to the surface of the galvanized coating.
Alternatively, it can be performed by electrolysis such as cathodic or anodic electrolysis
in an alkaline solution (alkali electrolysis) or cathodic electrolysis in a neutral
solution. The post-galvanizing surface treatment can also be performed by skin-pass
rolling using a strong alkali solution or an acid which can dissolve aluminum oxide
as a skin-pass rolling liquid or by cooling a hot galvanized or alloyed steel sheet
with an alkali solution as a cooling medium before skin-pass rolling.
[0023] A continuous plating line according to the present invention comprises a continuous
hot-galvanizing apparatus for forming a galvanized coating on a steel strip which
is optionally equipped with an alloying apparatus, a continuous electroplating apparatus
connected in series with the hot-galvanizing apparatus for forming an electroplated
coating on the galvanized coating, and at least one post-galvanizing surface treatment
apparatus disposed between the hot-galvanizing apparatus and the electroplating apparatus
for removing surface oxide contaminants and activating the surface of the galvanized
coating.
[0024] For example, the post-galvanizing surface treatment apparatus can be a device for
spraying a steel strip with a surface treatment solution such as a strong alkali solution
or an acid which can dissolve aluminum oxide, an immersion bath using such a surface
treatment solution, an electrolytic cell, a cooling tank using an alkali solution
as a cooling medium which is disposed before a skin-pass rolling mill, or a skin-pass
rolling mill employing a strong alkali solution or an acid which can dissolve aluminum
oxide as a skin-pass rolling liquid.
Figure 1 is a schematic illustration of an embodiment of a continuous plating line
according to the present invention;
Figures 2a and 2b are schematic cross-sectional views of a multi-layer plated steel
sheet manufactured by the method of the present invention and by a conventional method,
respectively;
Figure 3 is a schematic illustration of another embodiment of a continuous plating
line according to the present invention;
Figure 4 is a graph of the relationship between the microcovering power of an electroplated
coating, the temperature of a post-galvanizing surface treatment solution, and the
temperature of a steel sheet during post-galvanizing surface treatment; and
Figure 5 is a schematic illustration of yet another embodiment of a continuous plating
line according to the present invention.
[0025] The present invention will be described in greater detail while referring to the
accompanying drawings. The drawings illustrate embodiments of the plating line of
the present invention having an alloying furnace after the hot-galvanizing bath. However,
an alloying step is optional and the present invention is not limited to such embodiments.
[0026] Figure 1 schematically illustrates a continuous plating line according to the present
invention.
[0027] As shown in this figure, a steel strip 2 is unwound from a pay-off reel 1 and passed
through a prewashing apparatus 3 and then through a pretreatment apparatus comprising
a rapid heating furnace 4, a reduction furnace 5, and a cooling furnace 6 in which
the surface of the steel strip is cleaned. If necessary, the strip 2 can be annealed.
It is then passed through a hot-galvanizing bath 7 where hot galvanizing is carried
out and a galvanizing coating is formed on one side or both sides of the strip. Then,
if necessary, the strip 2 is passed through an alloying furnace 8 in which Fe in the
steel strip 2 and Zn in the hot-galvanized coating are alloyed.
[0028] The hot-galvanizing bath 7 can be a bath of either zinc or a zinc alloy such as GALFAN
[5% Al, 0.1% (La + Ce), the remainder Zn], GALVALUME (55% Al, 1.5% Si, the remainder
Zn), or the like.
[0029] The optionally alloyed galvanized steel strip 2 is then passed through a post-galvanizing
surface treatment apparatus 9, which removes surface oxide contaminants and activates
the surface of the galvanized coating. In the present embodiment, the surface treatment
apparatus comprises a tank containing a strong alkali solution (pH at least 12) in
which the strip 2 is immersed. The strip 2 is then washed with a water scrubber 10
or similar water rinsing apparatus and passed through bridle rolls 19, a skin-pass
rolling mill 11, and a leveller 12 to flatten the surface and remove strains. The
strip 2 is then passed through a pretreatment tank 13 and an electroplating cell 14,
in which electroplating is performed on the galvanized coating. It is next rinsed
with water in a water scrubber 15 and then dried in a drier 16. Then, if necessary,
finishing treatment such as chromate treatment can be performed in a finishing surface
treatment apparatus 17, and the treated steel strip 2 is wound onto a tension roll
18.
[0030] The location of the post-galvanizing surface treatment apparatus 9 (and the water
scrubber 10) in the plating line is not critical. For example, it can be disposed
between the leveller 12 and the bridle rolls 19, in which case the post-galvanizing
surface treatment is performed after skin-pass rolling instead of before.
[0031] Furthermore, more than one post-galvanizing surface treatment apparatus 9 can be
employed. For example, an additional post-galvanizing surface treatment apparatus
9 and water scrubber 10 can be disposed between the leveller 12 and the bridle rolls
19, in which case the post-galvanizing surface treatment is performed both before
and after skin pass rolling.
[0032] The position of the skin-pass rolling mill 11 is also not critical. For example,
the skin-pass rolling mill 11 and the leveller 12 can be disposed between the drier
16 and the surface treatment apparatus 17, in which case skin-pass rolling is performed
subsequent to electroplating.
[0033] Furthermore, as mentioned previously, the post-galvanizing surface treatment apparatus
9 is not limited to an immersion tank, and it can be any device which is capable of
removing oxide contaminants from the surface of the galvanized coating of the steel
strip 2 and improving the adhesion of an electroplated coating deposited thereon.
For example, it can be a spraying apparatus, an electrolytic cell, or a skin-pass
rolling mill using a suitable post-galvanizing surface treatment solution as a skin-pass
rolling liquid.
[0034] The operation of the embodiment illustrated in Figure 1 will now be described.
[0035] First, if necessary, a steel strip 2 is washed in the prewashing apparatus 3 using
an alkali solution or other suitable rinse solution. It is then subjected to surface
cleaning and, if necessary, annealing in the pretreatment apparatus which consists
of the rapid heating furnace 4, the reduction furnace 5, and the cooling furnace 6.
[0036] In the cooling furnace 6, the temperature of the cleaned and optionally annealed
steel strip 2 is adjusted to a level suitable for hot-galvanizing, after which one
or both sides of the strip 2 are galvanized in a hot-galvanizing bath 7 containing
molten Zn or a molten Zn alloy to form a galvanized coating. The coating weight is
adjusted to a prescribed level by a gas wiping device disposed directly above the
galvanizing bath 7. The galvanized coating is then alloyed by heating in the alloying
furnace 8. Any type of alloying furnace 8 can be employed, such as a gas-heated furnace,
an electromagnetic induction furnace, or a laser heating furnace. The degree of alloying
is controlled by adjusting the temperature and the heating time.
[0037] In the manufacture of rust-preventive steel sheet for automobiles, the galvanized
coating typically has a Zn coating weight of 30 - 80 g/m² and it can be alloyed into
a Zn-Fe alloy containing 7 - 12% Fe. When alloying is not performed, the steel strip
2 can be simply passed through the alloying furnace without alloying treatment.
[0038] The surface of the resulting galvanized steel strip 2 is then subjected to post-galvanizing
surface treatment in the treatment apparatus 9. According to one form of the present
invention, the post-galvanizing surface treatment is performed with a strong alkali
solution by immersion or spraying.
[0039] Useful alkali solutions include sodium hydroxide, sodium silicate (ortho or meta),
sodium phosphate, and sodium bicarbonate solutions. When the post-galvanizing surface
treatment is performed by immersion or spraying, in order to achieve the desired effect
in a limited space and treating time, a strong alkali solution having a pH of at least
12, e.g., a 1M NaOH solution, is used preferably at a temperature of at least 50°C
and more preferably at least 60°C.
[0040] Post-galvanizing surface treatment can also be performed by electrolysis. The electrolysis
may be either in the form of cathodic or anodic electrolysis in a strong alkali solution
or a weak alkali solution (such as a sodium phosphate or sodium bicarbonate solution),
or cathodic electrolysis in a neutral solution (such as a sodium sulfate solution).
When performing electrolysis, a current can be directly applied between an electrode
and the strip, or an alternating current can be indirectly applied to the strip. The
temperature of the electrolytic solution is preferably at least 40 °C and more preferably
at least 50°C.
[0041] Post-galvanizing surface treatment of the galvanized steel strip can also be performed
by immersion or spraying with an acid which can dissolve aluminum oxide. Examples
of useful acids include hydrofluoric acid, phosphoric acid, and oxalic acid. Sulfuric
acid, hydrochloric acid, nitric acid, and the like have little ability to dissolve
aluminum oxide, while they can dissolve the galvanized coating on the steel strip
very rapidly, so they are not suitable. The acid preferably has a pH of 1 - 4 and
a temperature of at least 40 °C and more preferalby at least 50°C . If the pH is greater
than 4, treatment requires a long time, while if the pH is less than 1, the dissolution
of the galvanized coating is promoted, which is not desirable.
[0042] After the post-galvanizing surface treatment, the steel strip is rinsed with hot
or cold water in a rinse tank 10 which may be a water scrubber or a dip tank. The
remaining water can be removed from the surface of the strip using a ringer roll or
an air blower. The galvanized steel strip can then be subjected to coventional skin-pass
rolling by passing through a skin-pass rolling mill 11 and a leveller 12.
[0043] Temper rolling prevents buckling of a hot-galvanized steel strip and removes strains
caused by heating in the hot-galvanizing and alloying steps, and it flattens the surface
of the galvanized coating. It can be performed with a reduction of 0.1 - 2.0%, for
example. However, skin-pass rolling is not mandatory, and it can be omitted with certain
types of steel strips, such as with Ti-containing steel strip. With normal steel strip,
it is also possible to perform skin-pass rolling before the post-galvanizing surface
treatment or subsequent to electroplating, as described above.
[0044] When a skin-pass rolling mill 11 is employed in a continuous plating line according
to the present invention, the post-galvanizing surface treatment can be performed
during the water cooling stage prior to skin-pass rolling using an alkali solution
as a cooling medium.
[0045] After a steel strip is hot-galvanized and optionally alloyed, it is at a high temperature.
On the other hand, from the standpoint of the mechanical properties of the steel strip,
it is desirable that skin-pass rolling be performed in the vicinity of room temperature.
Therefore, the galvanized steel strip is normally cooled to room temperature by water
cooling prior to skin-pass rolling.
[0046] In one form of the present invention, an alkali solution is used as a cooling medium
to perform cooling prior to skin-pass rolling, whereby the galvanized steel strip
is cooled and simultaneously surface cleaning and activation of the galvanized coating
can be performed. For this purpose, at least two cooling tanks are disposed before
the skin-pass rolling mill. The cooling medium used in the last tank is water, but
in at least one of the other tanks an alkaline solution is employed as a cooling medium
and the galvanized steel strip is treated with the solution in that tank, thereby
improving the microcovering power of the subsequent electroplating.
[0047] Figure 5 illustrates an embodiment of a continuous plating line according to this
form of the present invention in which the post-galvanizing surface treatment apparatus
comprises an alkali solution cooling tank 9' which is followed by a water cooling
tank 10'. The structure of the plating line of this embodiment is otherwise the same
as that of the embodiment of Figure 1.
[0048] In the plating line of Figure 5, a steel strip 2 which has been hot-galvanized and
optionally alloyed and which is still hot is passed through the alkali solution cooling
tank 9' in which the surface of the galvanized coating of the strip 2 is cooled and
simultaneously cleaned and activated by immersing in or spraying with an alkali solution.
The strip 2 is then passed through the water cooling tank 10' for rinsing and further
cooling. The water rinsing in the final cooling tank 10' has no effect on the microcovering
power of an electroplated coating, but it is merely to remove the alkali component
adhering to the steel strip, thereby preventing the rolls and other equipment downstream
of this tank from contamination and corrosion.
[0049] The alkali solution is typically formed from sodium hydroxide or potassium hydroxide,
but other alkali compounds such as sodium carbonate, sodium bicarbonate, and sodium
orthosilicate can also be employed. The alkali solution may also contain a surfactant.
The pH of the alkali cooling solution is at least 10 in order to achieve the desired
effect.
[0050] The temperature of the steel strip 2 at the entrance to the alkali solution cooling
tank 9' is preferably at least 80 °C. If the strip temperature falls below 80°C ,
it is necessary for the pH of the solution to be 12 or higher. Thus, by performing
the post-galvanizing surface treatment during cooling of a hot alloyed or galvanized
steel strip, the surface cleaning and activation of a galvanized coating is promoted
due to the heat of the steel strip and can be accomplished in a short period with
an alkali solution of a lower pH.
[0051] Figure 4 shows the microcovering power of an electroplated coating when a hot-galvanized
steel strip is treated with a sodium hydroxide solution of pH 10 for 1 second with
different temperatures of the steel strip and the alkali solution. As can be seen
from this figure, the microcovering power greatly depends on the strip temperature
rather than the solution temperature. Accordingly, when the post-galvanizing surface
treatment is performed in the cooling stage by using an alkali solution as a cooling
medium immediately after the hot-galvanizing or alloying, the steel strip is still
hot, usually at a temperature above 80 °C , and the microcoverig power of an electroplated
coating can be improved by treatment with an alkali solution having a lower pH of
10 or above.
[0052] When the post-galvanizing treatment with an alkali solution is performed after the
galvanized steel strip has been cooled, it is undesirable to reheat the galvanized
steel strip, particularly after skin-pass rolling, from the standpoint of maintaining
the mechanical properties of the steel strip. Therefore, the alkali solution instead
of the steel strip is heated. However, as mentioned above, the rise in solution temperature
is less effective than that in strip temperature and it is preferable to use an alkali
solution having a higher pH of at least 12.
[0053] According to another form of the present invention, the post-galvanizing surface
treatment is performed during skin-pass rolling, using a strong alkali solution with
a pH of at least 12 or an acid which can dissolve aluminum oxide as a skin-pass rolling
liquid (lubricant).
[0054] Figure 3 schematically illustrates an embodiment of a continuous plating line according
to this form of the present invention in which the post-galvanizing surface treatment
apparatus is in the form of a skin-pass rolling mill 11. If necessary, this embodiment
can be further equipped with a water cooling tank (not shown) for cooling the steel
strip 2 to a suitable temperature for skin-pass rolling.
[0055] An example of a strong alkali solution which can be used as a skin-pass rolling liquid
is a 1M sodium hydroxide solution. However, any alkali solution can be used which
does not adversely affect the subsequent electroplating when a minor amount thereof
is introduced into the electroplating solution. A pH of at least 12 is effective,
but when performing mass production, the pH is preferably at least 12.5.
[0056] Examples of acids which can dissolve aluminum oxide and which can be used as a skin-pass
rolling liquid are as mentioned above and include hydrofluoric acid, phosphoric acid,
and oxalic acid having a pH of 1 - 4.
[0057] The skin-pass rolling liquid formed from a strong alkali solution or an acid can
be used by spraying onto the strip 2 or the work rolls of the skin-pass rolling mill.
The treating time may be varied by the distance between the skin-pass rolling mill
11 and ringer rolls (not shown) downstream of the mill. The effectiveness of post-galvanizing
surface treatment during skin-pass rolling is not significantly affected by manufacturing
conditions such as the travelling speed of the steel strip or the roughness of skin-pass
rolls. The temperature of the skin-pass rolling liquid is preferably at least 50 °C
.
[0058] It is known that an inhibitor may be added to water which is used as a skin-pass
rolling liquid during temper rollling after hot galvanizing of a steel strip. However,
the addition of an inhibitor is performed for the purpose of removing greases from
the steel strip and for preventing corrosion. It has no effect on the microcovering
power of an electroplated coating, and is thus totally different from the skin-pass
rolling liquid which can be employed in the present invention.
[0059] A skin-pass rolling liquid in the form of a strong alkali with a pH of at least 12
or an acid which can dissolve aluminum oxide chemically removes surface oxide contaminants
deposited on the galvanized coating which deteriorate the microcovering power of an
electroplated coating formed thereon. At the same time, these contaminants are mechanically
removed by the skin-pass rolling.
[0060] By performing the post-galvanizing surface treatment in one of the various above-mentioned
methods prior to electroplating, the adhesion and covering power of the electroplated
coating are greatly increased.
[0061] After the post-galvanizing surface treatment, the steel strip 2 is passed through
an electroplating apparatus to deposite an electroplated coating on the galvanized
coating. When both sides of the steel strip are galvanized, electroplating can be
applied to either one or both sides. When galvanizing is performed on one side of
the strip, usually electroplating is applied to the same side, i.e., on the galvanized
coating, although there is no limitation in this respect.
[0062] The electroplating apparatus includes the pretreatment tank 13, the electroplating
cell 14, and the washing tank 15 (a water scrubber). In the pretreatment tank 13,
the galvanized steel strip 2 is washed with water which may contain a certain additive
which improves the surface condition of the steel strip. In the electroplating cell
14, various types of electroplating can be performed. In the washing tank 15, the
electroplated steel strip is rinsed with water. If necessary, the steel strip 2 can
be dried with hot air or by electric heating in the drier 16.
[0063] The electroplated coating is not restricted to any particular type. For example,
it can be one which improves coatability of the galvanized coating by cationic electrodeposition
overlaid thereon such as a pure Fe or Fe-X coating (wherein X is Zn, P, Ni, B, Sn,
Ti or the like), a coating which improves the sliding properties of the galvanized
coating such as a Cr (Cr-oxide), Ni, Ni-Zn coating, or various dispersion-type coatings
such as a Ni-SiC, Zn-SiO₂, Ni-Zn-SiO₂, or a Zn-Al₂O₃ coating. Depending on the desired
coating weight, a plurality of electroplating cells can be used.
[0064] Next, if necessary, finishing surface treatment such as chromate treatment, zinc
phosphate treatment, or resin coating using a roll coater can be performed in the
finishing surface treatment apparatus 17 to obtain a finished product.
[0065] Normally, in an electroplating line, an alkali degreasing apparatus is installed
as a pre-treatment apparatus. Such an apparatus is used merely for the purpose of
removing dirt and grease (oil and fat) adhering to the steel strip, and its operation
and effects are totally different from those of The post-galvanizing surface treatment
employed in the present. invention.
[0066] A hot-galvanized coating sometimes contains elements such as Al, Mg, and Mn. The
post-galvanizing surface treatment of the present invention activates only the surface
of the galvanized coating and does not reach the inside of the coating, so there is
no adverse effect on these elements.
[0067] Figures 2a and 2b schematically illustrate the structure of a multi-layer coating
according to the present invention and the prior art, respectively. In the example
of the present invention (Figure 2a), minute irregularities 24 and 26 can be observed
in the alloyed hot-galvanized coating layer 22 formed on a steel strip 20, but an
electroplated coating 28 is uniformly formed over the irregularities. Surface contaminants
which obstruct electrodeposition are previously removed.
[0068] In contrast, in the example of the prior art (Figure 2b), the electroplated coating
layer 28 is able to cover the protrusions of the underlying alloyed galvanized coating
22, but the coating 22 is exposed where it contains depressions. Therefore, the coatability
and workability of the resulting steel strip are not adequately improved by the electroplated
coating.
(Examples)
[0069] The present invention will now be described in further detail by the following examples.
Example 1
[0070] Continuous hot-galvanizing and electroplating were carried out using a continuous
plating line like that illustrated in Figure 1. The plating line was equipped with
an additional post-galvanizing surface treatment apparatus between the leveller 12
and the bridle rolls 19 such that post-galvanizing surface treatment could be performed
either before or after skin-pass rolling. Both sides of a steel strip were hot-galvanized
with a coating weight of 45 g/m² for each side and then alloyed. Post-galvanizing
surface treatment was performed under the conditions given in Table 1 and after or
before that the galvanized strip was temper-rolled using water which might contain
a conventional inhibitor as a skin-pass rolling liquid. Electroplating was performed
on both sides of the galvanized coating with a coating weight of 4 g/m² for each side.
The plating conditions were otherwise normal ones.
[0071] In Table 1, A - F indicate the following treatment conditions.
(A) Immersion in an Alkaline Solution
alkali solution used: 2M NaOH solution
temperature: 70 °C
treatment time: 2 seconds
(B) Alkali Electrolysis
alkali electrolytic solution: 1M NaOH solution
temperature: 70 °C
cathodic electrolysis: 20 A/dm²
treatment time: 2 seconds
(C) Neutral Cathodic Electrolysis
neutral electrolytic solution: 0.5M Na₂SO₄ solution
temperature: 70 °C
cathodic electrolysis: 60 A/dm²
treatment time: 5 seconds
(D) Spraying with an Alkaline Solution
spray solution: 1M NaOH solution
temperature: 70 °C
spray header pressure: 0.5 kg/cm²
treatment time: 2 seconds
(E) Immersion in an Acid
acid solution: 0.5M phosphoric acid solution
temperaturep: 70°C
treatment time: 3 seconds
(F) Spraying with an Acid
acid solution: 0.5M oxalic acid solution
temperature: 60 °C
treatment time: 3 seconds
If necessary, chromate treatment was performed in a finishing surface treatment
apparatus 17 after electroplating to obtain a finished product.
[0072] The adhesion and microcovering power of the electroplated coating are shown in Table
1.
[0073] The adhesion of the electroplated coating was measured by an adhesive tape peel test
after the test piece was subjected to 0T 180° bending. The microcovering power of
the electroplated coating was evaluated by microscopic observation of a cross section
and an EPMA (electron probe microanalyzer). The rating in these tests are as follows:
adhesion |
microcovering power |
⃝ (good) no peeling |
complete covering over irregular surfaces |
△ (fair) slight peeling |
small uncovered areas |
X (poor) peeling |
large uncovered areas |

[0074] As is clear from Table 1, the electroplated coating of the resulting multi-layer
plated steel strip according to the present invention had excellent adhesion and microcovering
power. The microcovering power in particular was far superior to that of a conventional
coating.
Example 2
[0075] A 0.8 mm-thick GA (alloyed galvanized) steel strip having a galvanized coating of
45 g/m² on both sides which was manufactured by a commercial galvanizing line and
which had not been treated with an oil or a chromate or other surface treatment solution
was subjected to post-galvanizing surface treatment by immersion in various solutions
shown in Table 2. Thereafter, Fe-Zn electroplating was performed on both sides under
the following conditions. The microcovering power of the resulting electroplated coating
was evaluated by microscopic observation of a cross section and an EPMA. The results
are shown in Table 2. In Table 2, an ⃝ indicates that the plating was able to cover
the irregularities in the GA layer as shown in Figure 2a, while an X indicates that
the electroplated layer was discontinuous as shown in Figure 2b.
Electroplating conditions:
[0076]
Sulfate bath |
Total Fe |
80 g/l, |
current density: |
60 A/dm² |
Fe³⁺ |
1000 ppm, |
plating weight: |
5 g/m² |
Zn²⁺ |
2 g/l, |
pH: |
1.6 |
Na⁺ |
25 g/l |
Temperature: |
50°C |
TABLE 2
No. |
Immersion solution |
pH |
Temp. (°C) |
Treating time (sec.) |
Microcovering power |
1 |
NaOH |
13.5 |
60 |
1 |
⃝ |
2 |
NaOH |
12.5 |
60 |
1 |
⃝ |
3 |
NaOH |
12.0 |
60 |
2 |
⃝ |
4 |
NaOH |
11.0 |
60 |
2 |
X |
5 |
NaOH |
11.0 |
60 |
4 |
X |
6 |
HF |
3.0 |
60 |
2 |
⃝ |
7 |
H₃PO₄ |
4.0 |
60 |
2 |
⃝ |
8 |
Oxalic acid |
3.0 |
60 |
2 |
⃝ |
9 |
H₂SO₄ |
3.0 |
60 |
2 |
X |
10 |
HCl |
3.0 |
60 |
2 |
X |
11 |
Thinner |
― |
20 |
10 |
X |
12 |
Water |
― |
60 |
4 |
X |
13 |
Water + Inhibitor |
― |
60 |
4 |
X |
[0077] For samples No. 4 and No. 5, the weak alkali treatment was carried out with a pH
of less than 12, and samples No. 9 and 10 used an acid which could not dissolve aluminum
oxide. Samples Nos. 11 - 13 illustrate conventional methods. In each of these samples,
the aluminum oxide on the surface of the GA layer could not be dissolved and therefore
the microcovering power was poor. In contrast, in samples Nos. 1 - 3 and 6 - 8 of
the present invention, post-galvanizing surface treatment was able to dissolve the
aluminum oxide on the surface of the GA coating without dissolving the GA coating
itself, so the microcovering power was excellent.
Example 3
[0078] Hot-galvanizing followed by electroplating was performed on both sides of a steel
strip using an apparatus like that illustrated in Figure 3. The coating weight of
the galvanized Zn layer was 45 g/m² for each side. A 1M NaOH solution at a temperature
of 50 °C with a pH of 13.5 was used as a skin-pass rolling liquid during skin-pass
rolling of the alloyed galvanized strip which was performed with a reduction of 0.6%.
Continuous electroplating was carried out under the same conditions as for Example
2. The resulting plating had good microcovering power.
[0079] In contrast, when water (or water + an inhibitor) at 50°C or when an NaOH solution
with a pH of 11.0 was used as a skin-pass rolling liquid, the electroplated layer
formed atop the GA coating had poor microcovering power.
Example 4
[0080] An alloyed galvanized steel strip similar to that used in Example 2 was heated to
various temperatures and treated for 1.0 second with an NaOH solution with a pH of
10.0 heated at various temperatures. The strip was then washed with water, after which
it was electroplated under the following conditions. The effects of the temperatures
of the alkali solution and the steel strip on the microcovering power of the resulting
electroplated layer are shown in Figure 4.
Electroplating conditions
[0081]
Total Fe |
70 g/l |
Current density |
50 A/dm² |
Fe³⁺ |
2 g/l |
Plating weight |
5 g/m² |
Zn²⁺ |
1.5 g/l |
Temperature |
50 °C |
pH |
1.8 |
|
|
[0082] It was confirmed that the temperature of the steel strip more greatly affect the
microcovering power than the temperature of the alkali solution. The higher the temperature
of the steel strip the better. Satisfactory results were obtained when the strip temperature
is higher than 80°C .
Example 5
[0083] An alloyed galvanized steel strip similar to that used in Example 2 was treated under
the conditions shown in Table 3 and then washed with water. It was then electroplated
under the same conditions as in Example 4.
[0084] The results are shown in Table 3.
TABLE 3
No. |
Immersion solution |
pH |
Solution temp. (°C) |
Strip temp. (°C) |
Treating time (sec.) |
Microcovering power |
1 |
NaOH |
10 |
80 |
80 |
1.0 |
⃝ |
2 |
NaOH |
10 |
80 |
100 |
0.5 |
⃝ |
3 |
NaOH |
10 |
80 |
150 |
0.5 |
⃝ |
4 |
NaOH |
10 |
80 |
200 |
0.5 |
⃝ |
5 |
NaOH |
12 |
80 |
100 |
0.5 |
⃝ |
6 |
NaOH |
9 |
80 |
100 |
1.0 |
X |
7 |
Na₄SiO₄ |
10 |
80 |
100 |
1.0 |
⃝ |
8 |
Water |
― |
80 |
150 |
1.0 |
X |
[0085] The electroplated layer of the resulting multi-layer plated steel strip obtained
by the method of the present invention had excellent microcovering power.
Example 6
[0086] Using the apparatus shown in Figure 5, an alloyed hot-galvanized steel strip was
subjected to cooling using a NaOH solution with a pH of 10.0 as a cooling medium in
an alkali solution cooling tank 9' and then washed with water in a water cooling tank
10'. It was then electroplated under the same conditions as in Example 4. The alkali
solution cooling conditions were as follows:
Strip temperature upon entry: |
90 °C |
Alkali solution temperature: |
85 °C |
Treatment time: |
0.6 seconds |
[0087] The electroplated layer of the resulting multi-layer plated steel strip had good
microcovering power.
[0088] For comparison, plating was carried out in the same manner as above except that alkali
solution cooling was not performed. The resulting electroplated layer had poor microcovering
power.
Example 7
[0089] The procedure described in Example 2 was repeated except that the post-galvanizing
surface treatment of a GA steel strip was performed by cathodic or anodic electrolysis
under the conditions shown in Table 4. The electrolytic solutions used were a 1M sodium
sulfate solution, a 1M ammonium chloride solution, both neutral, and a 1M sodium sulfate
solution which had been adjusted to pH 11. The results are shown in Table 4.
TABLE 4
|
Electrolytic solution |
Electrolysis conditions |
Treating time |
Microcoverring power |
1 |
1M Na₂SO₄ (neutral, 50°C) |
Cathodic, 40 A/dm² |
2 sec |
⃝ |
2 |
1M NH₄Cl (neutral, 50°C |
Cathodic, 40 A/dm² |
2 sec |
⃝ |
3 |
1M Na₂SO₄ (pH 11, 50°C) |
Cathodic, 40 A/dm² |
2 sec |
⃝ |
4 |
1M Na₂SO₄ (pH 11, 50°C) |
Anodic, 40 A/dm² |
2 sec |
⃝ |
5 |
1M Na₂SO₄ (neutral, 50°C) |
Anodic, 40 A/dm² |
2 sec |
X |
[0090] From the preceding examples, it can be seen that by performing post-galvanizing surface
treatment on a galvanized steel strip before electroplating according to the present
invention, an electroplated coating having excellent adhesion and microcovering power
can be obtained.