[Technical Field of the Invention]
[0001] The present invention relates to a chemical treatment steel sheet and a method for
manufacturing a chemical treatment steel sheet.
[Background Art]
[0002] Corrosion is occurred when metals are continuously used in some cases. Various techniques
have been proposed to prevent corrosion of metals. Examples of the proposed techniques
include a technique of applying plating to a metal plate or a technique of performing
various surface treatments on the surface of a metal plate of a plated surface.
[0003] For example, Patent Document 1 describes a technique of forming an organic resin
film including a vanadium compound or at least one of a phosphate and phosphate-based
compound, a silane compound having at least one of an epoxy group and an amino group,
and an organic resin including at least one of a water-soluble organic resin and a
water-dispersible organic resin as main components on a surface of an Al-Zn-based
alloy plated steel sheet used for building materials and home appliances.
[0004] On the other hand, when metal containers for the purpose of preserving beverages
or foods are manufactured, Ni-plated steel sheets, Sn-plated steel sheets, Sn-based
alloy plated steel sheets, or the like have been used. The Al-Zn-based alloy plated
steel sheet described in Patent Document 1 is a so-called sacrificial protection steel
sheet, whereas a Ni-plated steel sheet, a Sn-plated steel sheet, or a Sn-based alloy
plated steel sheet is a so-called barrier plated steel sheet.
[0005] When a Ni-plated steel sheet, a Sn-plated steel sheet, or a Sn-based alloy plated
steel sheet is used as a steel sheet for a metal container for the purpose of preserving
beverages or foods (hereinafter referred to as a "steel sheet for containers"), the
surface of the plated steel sheet is subjected to a chemical treatment using hexavalent
chromium to secure adhesiveness and corrosion resistance between the steel sheet and
a coating or a film in many cases. A chemical treatment using a solution containing
a hexavalent chromium is referred to as a chromate treatment.
[0006] However, since hexavalent chromium used in a chromate treatment is harmful to the
environment, a chemical treatment film such as a Zr-phosphate film has been developed
as a replacement for the chromate treatment applied to a steel sheet for containers
in the related art. For example, Patent Document 2 describes a steel sheet for containers
having a chemical treatment film including Zr, a phosphate, a phenolic resin, and
the like.
[0007] Examples of foods preserved in a metal container using a steel sheet for containers
include meat, vegetables, and the like. Meat and vegetables contain various proteins,
but these proteins contain amino acids containing sulfur (sulfur-containing amino
acids represented by L-cysteine, L-methionine, and L-(-)-cystine) in some cases. When
foods containing sulfur-containing amino acids is heated during sterilization, S in
the sulfur-containing amino acids binds to Sn, Fe, or the like in a steel sheet for
containers, resulting in black discoloration. This phenomenon is referred to as "sulfide
stain." Since the appearance of the inner surface of a metal container deteriorates
when sulfide stain occurs, countermeasures have been sought to prevent the occurrence
of sulfide stain.
[0008] In addition, Patent Document 3 describes a method for manufacturing a steel sheet
for containers in which a Zr-containing film is formed on a surface of a steel sheet
by immersing the steel sheet or performing an electrolytic treatment on the steel
sheet in a solution containing Zr ions, F ions, and at least one reaction accelerating
component selected from the group consisting of Al ions, boric acid ions, Cu ions,
Ca ions, Al metal, and Cu metal.
[Citation List]
[Patent Documents]
[0009]
[Patent Document 1]
Japanese Unexamined Patent Application, First Publication No. 2005-290535
[Patent Document 2]
Japanese Unexamined Patent Application, First Publication No. 2007-284789
[Patent Document 3]
Japanese Unexamined Patent Application, First Publication No. 2012-62521
[Summary of Invention]
[Problems to be Solved by the Invention]
[0010] Since a film formed through a chromate treatment (hereinafter referred to as a "chromate
film") is dense even when an adhered amount of film is small, a steel sheet for containers
having a chromate film formed on its surface has excellent corrosion resistance and
sulfide stain resistance. However, since hexavalent chromium is harmful to the environment
as described above, a steel sheet for containers should preferably not contain hexavalent
chromium as far as possible.
[0011] On the other hand, the organic resin film described in Patent Document 1 and the
chemical treatment film described in Patent Document 2 do not contain hexavalent chromium
and thus are appropriate for the environment. However, in the organic resin film described
in Patent Document 1 and the chemical treatment film described in Patent Document
2, it is necessary to increase an adhered amount of film to form a dense film which
can obtain appropriate sulfide stain resistance. An increase in adhered amount of
film is not preferable because, when an adhered amount of film is increased, the adhesion
between the film and a plated layer under the film decreases and the weldability of
the chemical treatment steel sheet decreases, which is not preferable. Furthermore,
an increase in adhered amount of film is not economically preferable.
[0012] In the method for manufacturing a steel sheet for containers described in Patent
Document 3, the Al content in the chemical treatment film is small. Thus, it is difficult
to obtain an appropriate sulfide stain resistance in some cases.
[0013] The present invention was made in view of the above-described circumstances and an
objective of the present invention is to provide a chemical treatment steel sheet
which has excellent corrosion resistance and sulfide stain resistance even when an
amount of chemical treatment layer adhered is small and a method for manufacturing
the same.
[Means for Solving the Problem]
[0014] The present invention employs the following means to solve the above-described problems
and achieve the above objective.
- (1) A chemical treatment steel sheet according to an aspect of the present invention
includes a steel sheet, an Fe-Sn alloy layer which is formed on at least one surface
of the steel sheet, a Sn layer which is formed on the Fe-Sn alloy layer and contains
Sn in which an total amount of Sn contained in the Fe-Sn alloy layer and the Sn layer
is 0.10 to 30.0 g/m2, and a chemical treatment layer which is formed on the Sn layer and contains a Zr
compound in which an amount of Zr contained therein is 1.0 to 150 mg/m2, a phosphate compound in which an amount of P contained therein is 1.0 to 100 mg/m2 and an Al compound in which an amount of Al contained therein is 0.10 to 30.0 mg/m2.
- (2) In the chemical treatment steel sheet according to (1) above, the chemical treatment
layer may contain Al2O3 in which an amount of Al contained therein is 0.10 to 30.0 mg/m2.
- (3) In the chemical treatment steel sheet according to (1) or (2) above, the chemical
treatment layer may contain the Zr compound in which an amount of Zr contained therein
is 1.0 to 120 mg/m2, the phosphate compound in which an amount of P contained therein is 2.0 to 70.0
mg/m2, and the Al compound in which an amount of Al contained therein may be 0.20 to 20.0
mg/m2.
- (4) In the chemical treatment steel sheet described according to any aspect of (1)
to (3), the total amount of Sn contained in the Fe-Sn alloy layer and the Sn layer
may be 0.30 to 20.0 g/m2.
- (5) In the chemical treatment steel sheet described according to any aspect of (1)
to (4), a surface of the chemical treatment layer may not be covered with a film or
a coating material.
- (6) A method for manufacturing a chemical treatment steel sheet according to an aspect
of the present invention includes a plating process of forming a Sn-plated layer containing
Sn in which an amount of Sn contained therein is 0.10 to 30.0 g/m2 on a surface of a steel sheet, a reflow treatment process of forming an Fe-Sn alloy
layer and a Sn layer by performing reflow treatment on the Sn-plated layer, and an
electrolytic treatment process of forming a chemical treatment layer on the Sn layer
by performing electrolytic treatment under conditions of a current density of 1.0
to 100 A/dm2 and an electrolytic treatment time of 0.20 to 150 seconds using a chemical treatment
solution having a temperature of 5°C or higher and lower than 90°C. The chemical treatment
solution contains 10 to 20,000 ppm of Zr ions, 10 to 20,000 ppm of F ions, 10 to 3000
ppm of phosphate ions, 100 to 30,000 ppm of nitrate ions and sulfate ions in total,
and 500 to 5,000 ppm of Al ions, and may be used (NH4)3AlF6 as a supply source of Al ions.
- (7) In the method for manufacturing a chemical treatment steel sheet according to
(6) above, the chemical treatment solution may contain 200 to 17,000 ppm of the Zr
ions, 200 to 17,000 ppm of the F ions, 100 to 2.000 ppm of the phosphate ions, 1000
to 23,000 ppm of the nitrate ions and the sulfate ions in total, and 500 to 3,000
ppm of the Al ions.
[Effects of the Invention]
[0015] According to each aspect described above, a chemical treatment steel sheet having
an excellent corrosion resistance and sulfide stain resistance even in a case in which
an adhered amount of a chemical treatment layer is small and a method for manufacturing
the chemical treatment steel sheet can be provided.
[Brief Description of the Drawing(s)]
[0016]
Fig. 1A is a schematic diagram showing a chemical treatment steel sheet in which a
Fe-Sn alloy layer, a Sn layer, and a chemical treatment layer are formed on one surface
of a steel sheet.
Fig. 1B is a schematic diagram showing a chemical treatment steel sheet in which Fe-Sn
alloy layers, Sn layers, and chemical treatment layers are formed on both surfaces
of a steel sheet.
Fig. 2 is a flowchart showing an example of a flow of a method for manufacturing a
chemical treatment steel sheet.
Fig. 3 is a graph showing results of Example 1.
[Embodiments of the Invention]
[0017] Exemplary embodiments of the present invention will be described in detail below
with reference to the appended drawings. Note that, in the present embodiments, repeated
description will be omitted by giving the same reference symbols to constituent elements
having similar configurations.
<Regarding configuration of chemical treatment steel sheet>
[0018] First, a configuration of a chemical treatment steel sheet according to an embodiment
will be described in detail with reference to Fig. 1A and Fig. 1B. Fig. 1A and Fig.
1B are explanatory diagrams schematically showing layer structures of the chemical
treatment steel sheet according to the present embodiment.
[0019] The chemical treatment steel sheet 10 according to the present embodiment has steel
sheets 103, Fe-Sn alloy layers 105a, Sn layers 105b, and chemical treatment layers
107 as shown in Fig. 1A and Fig. 1B.
(Regarding steel sheet 103)
[0020] The steel sheet 103 is used as a base material for the chemical treatment steel sheet
10 according to the present embodiment. The steel sheet 103 used in the present embodiment
is not particularly limited, and a known steel sheet 103 that is used as a steel sheet
for containers can be used. A method for manufacturing the steel sheet 103 and a material
thereof are not particularly limited either, and a steel sheet 103 produced through,
beginning from a general steel piece production process, a known process such as hot
rolling, pickling, cold rolling, annealing, or temper rolling can be used.
[0021] A thickness of the steel sheet 103 is preferably 0.05 to 1 mm in consideration of
practicability and economic efficiency when it is used as a steel sheet for containers.
[Regarding Fe-Sn alloy layer 105a and Sn layer 105b]
[0022] The Fe-Sn alloy layer 105a and the Sn layer 105b containing Sn are formed on a surface
of the steel sheet 103. The Fe-Sn alloy layer 105a and the Sn layer 105b are barrier
plated layers. A barrier plated layer is a plated layer in which the corrosion of
the steel sheet 103 is suppressed by preventing a cause of corrosion from acting on
the base material by means of forming a metal film of Sn on the surface of the steel
sheet 103 using Sn which are metals more electrochemically noble than Fe constituting
the steel sheet 103 which is the base material.
[0023] On the other hand, a sacrificial protection layer has a function opposite to that
of a barrier plated layer. In a sacrificial protection layer, the corrosion of the
steel sheet 103 is suppressed by corroding a metal such as Zn constituting the plated
layer earlier than Fe constituting the steel sheet 103 by mean of forming a metal
film on the surface of the steel sheet 103 using a metal less electrochemically noble
than Fe constituting the steel sheet 103 serving as the base material (for example
Zn as in Patent Document 1). The interaction between the barrier plated layer and
the chemical treatment layer 107 is different from that between the sacrificial protection
layer and the chemical treatment layer 107.
[0024] Specific examples of the Fe-Sn alloy layer 105a and the Sn layer 105b according to
the present embodiment will be described below with reference to Fig. 1A and Fig.
1B.
[0025] Note that the Fe-Sn alloy layer 105a, the Sn layer 105b, and the chemical treatment
layer 107 may be formed on one surface of the steel sheet 103 as shown in Fig. 1A,
and the Fe-Sn alloy layers 105a, the Sn layers 105b, and the chemical treatment layer
107 may be formed on both surfaces of the steel sheet 103 as shown in Fig. 1B.
[0026] The Fe-Sn alloy layer 105a is formed on the surface of the steel sheet 103, and the
Sn layer 105b is formed on the Fe-Sn alloy layer 105a as shown in Fig. 1A and Fig.
1B. Although details will be described below, the Fe-Sn alloy layer 105a and the Sn
layer 105b are formed by forming a Sn-plated layer (not shown) on the surface of the
steel sheet 103 and then performing reflow treatment (reflow treatment) thereon.
[0027] The Sn-plated layer (not shown) is formed to secure corrosion resistance and weldability
of the chemical treatment steel sheet 10. Regarding Sn, not only does Sn itself having
high corrosion resistance, but Fe-Sn alloys contained in the Fe-Sn alloy layer 105a
also have excellent corrosion resistance and weldability.
[0028] Although both the Fe-Sn alloy layer 105a and the Sn layer 105b according to the present
embodiment contain Sn, the total amount of Sn contained in the Fe-Sn alloy layer 105a
and the Sn layer 105b is 0.10 to 30.0 g/m
2 per one surface.
[0029] Sn has excellent processability, weldability, and corrosion resistance, and by performing
the reflow treatment after Sn plating, corrosion resistance of the chemical treatment
steel sheet 10 can be further improved, and a surface appearance (mirror appearance)
of the chemical treatment steel sheet 10 can be made more preferable. In order to
obtain the above-described effects, it is necessary for the total amount of Sn contained
in the Fe-Sn alloy layer 105a and the Sn layer 105b be 0.10 g/m
2 per one surface.
[0030] In addition, when the amount of Sn increases further, processability, weldability,
and corrosion resistance of the chemical treatment steel sheet 10 are improved, but
if the total amount of Sn in the Fe-Sn alloy layer 105a and the Sn layer 105b exceeds
30.0 g/m
2 per one surface, the above-described effects from Sn are saturated. In addition,
if the total amount of Sn in the Fe-Sn alloy layer 105a and the Sn layer 105b exceeds
30 g/m
2 per one surface, it is not economically preferable. For the above-described reasons,
the total amount of Sn contained in the Fe-Sn alloy layer 105a and the Sn layer 105b
is set to be 30.0 g/m
2 or less per one surface.
[0031] It is preferable for the total amount of Sn in the Fe-Sn alloy layer 105a and the
Sn layer 105b be 0.30 g/m
2 to 20.0 g/m
2 per one surface. When the total amount of Sn in the Fe-Sn alloy layer 105a and the
Sn layer 105b is 0.30 g/m
2 or more per one surface, the above-described effects from Sn can be obtained more
reliably. In addition, when the total amount of Sn in the Fe-Sn alloy layer 105a and
the Sn layer 105b is 20.0 g/m
2 or less per one surface, production costs can be reduced further.
[0032] The Fe-Sn alloy layer 105a contains Fe in which an amount of Fe contained therein
is 0.0010 to 100 g/m
2. In addition, the Fe-Sn alloy layer 105a may contain trace elements and inevitable
impurities that are incorporated thereinto during a production process or the like,
in addition to Sn and Fe.
[0033] In the Fe-Sn alloy layer 105a, a total amount of Fe metal and Sn metal contained
is 50 mass% or more. In the Fe-Sn alloy layer 105a, a total amount of Fe metal and
Sn metal to be contained is preferably 70 mass% or more.
[0034] The Sn layer 105b may contain only Sn, or may contain Fe in which an amount of Fe
contained therein is 0.0010 to 6.0 g/m
2. In addition, the Sn layer 105b may contain trace elements and inevitable impurities
that are incorporated thereinto during a production process or the like.
[0035] In addition, the amount of Sn contained in the Sn layer 105b is 50 mass% or higher.
The amount of Sn contained in the Sn layer 105b is preferably 70 mass% or higher.
[0036] A ratio between thicknesses of the Fe-Sn alloy layer 105a and the Sn layer 105b is
not particularly limited, and any ratio is possible as long as the above-described
amount of Sn is secured.
[0037] However, when the steel sheet 103 having the surface on which the Fe-Sn alloy layer
105a and the Sn layer 105b are formed is used as a steel sheet for containers, it
is difficult to prevent sulfide stain even if a film is laminated on a surface of
the Sn layer 105b or a coating material is applied thereon. It is thought that S contained
in contents such as beverages and foods binds to Sn and that black SnS, SnS
2 or the like is formed.
[0038] Note that S is contained in beverages and food as a constituent element of S-containing
amino acids such as L-cysteine, L-(-)-cystine, and L-methionine.
[0039] In addition, in a case where the Fe-Sn alloy layer 105a and the Sn layer 105b are
formed not to be dense, part of the steel sheet 103 as a base material is exposed.
In such a case, there are cases in which Fe contained in the steel sheet 103 bonds
with S contained in a beverage, food, or the like, and black FeS, Fe
2S
3, and Fe
2S are formed.
[0040] In order to reduce the blackening caused by SnS, SnS
2, FeS, Fe
2S
3, Fe
2S, or the like, a chromate film has previously mainly been formed on the surfaces
of the Fe-Sn alloy layer 105a and the Sn layer 105b.
[0041] In order to improve sulfide stain resistance, the chemical treatment layer 107 containing
a Zr compound, a phosphate compound, and an Al compound is formed on the surfaces
of the Fe-Sn alloy layer 105a and the Sn layer 105b as a substitute for the conventional
chromate film in the chemical treatment steel sheet 10 according to the present embodiment.
[Regarding chemical treatment layer 107]
[0042] The chemical treatment layers 107 are formed on the surfaces of the Sn layer 105b
as shown in Fig. 1A and Fig. 1B. The chemical treatment layer 107 is a composite film
layer having the Zr compound as a main component, containing the Zr compound in which
an amount of Zr contained therein is 1.0 to 150 mg/m
2 per one surface, the phosphate compound in which an amount of P contained therein
is 1.0 to 100 mg/m
2 per one surface, and the Al compound in which an amount of Al contained therein is
0.10 to 30.0 mg/m
2 per one surface.
[0043] Note that, in the present embodiment, a composite film layer indicates a film layer
in which a Zr compound, a phosphate compound, and an Al compound are in a partially
mixed state without being fully mixed.
[0044] In a case where three films such as a Zr film containing the Zr compound, a phosphate
film containing the phosphate compound, and an Al film containing the Al compound
are formed to be stacked on the Sn layer 105b, although a certain degree of effects
relating to corrosion resistance and adhesiveness is obtained, they are practically
insufficient. However, if the Zr compound, the phosphate compound, and the Al compound
are partially mixed in the chemical treatment layer 107 as described in the present
embodiment, better corrosion resistance and adhesiveness can be obtained than in the
case in which the three films are formed to be stacked as described above.
[0045] The Zr compound contained in the chemical treatment layer 107 according to the present
embodiment has a function of improving corrosion resistance, adhesiveness, and process
adhesiveness. As the Zr compound according to the present embodiment, a Zr oxide,
a Zr phosphate, a Zr hydroxide, a Zr fluoride, and the like are exemplary examples,
and the chemical treatment layer 107 may contain multiple above-described Zr compounds.
A preferable combination with the Zr compound is a Zr oxide, a Zr phosphate, and a
Zr fluoride.
[0046] In a case where the amount of Zr contained in the chemical treatment layer 107 is
1.0 mg/m
2 or more per one surface, practically preferable corrosion resistance, adhesiveness,
and process adhesiveness are secured.
[0047] Meanwhile, as the amount of Zr in the Zr compound increases, corrosion resistance,
adhesiveness, and process adhesiveness are improved accordingly. However, if the amount
of Zr contained in the Zr compound exceeds 150 mg/m
2 per one surface, the chemical treatment layer 107 becomes excessively thick, and
due to the main cause of a cohesive fracture, adhesiveness of the chemical treatment
layer 107 to the Sn layer 105b deteriorates, electrical resistance increases, and
weldability is degraded. In addition, if the amount of Zr contained in the Zr compound
exceeds 150 mg/m
2, adhesion of the chemical treatment layer 107 becomes uneven, which may cause an
irregular appearance.
[0048] Thus, the amount of Zr contained in the Zr compound (i.e., the amount of Zr) of the
chemical treatment layer 107 according to the present embodiment is set to 1.0 mg/m
2 to 150 mg/m
2 per one surface. The amount of Zr contained in the Zr compound is preferably 1.0
mg/m
2 to 120 mg/m
2 per one surface. By setting the amount to 120 g/m
2 per one surface, the production costs of the chemical treatment layer 107 can be
reduced further.
[0049] The chemical treatment layer 107 further contains one or more types of phosphate
compounds in addition to the above-described Zr compounds.
[0050] A phosphate compound according to the present embodiment has a function of improving
corrosion resistance, adhesiveness, and process adhesiveness. As the phosphate compound
according to the present embodiment, Fe phosphate, Ni phosphate, Sn phosphate, Zr
phosphate, Al phosphate, and the like which are formed when phosphate ions react with
compounds contained in the steel sheet 103, the Fe-Sn alloy layer 105a, the Sn layer
105b, and the chemical treatment layer 107 are exemplary examples. The chemical treatment
layer 107 may contain one or more types of the above-described phosphate compounds.
[0051] When the amount of phosphate compounds contained in the chemical treatment layer
107 is greater, corrosion resistance, adhesiveness, and process adhesiveness of the
chemical treatment steel sheet 10 are improved. Specifically, in a case where the
amount of P contained in the phosphate compound contained in the chemical treatment
layer 107 is 1.0 mg/m
2 or more, practically preferable corrosion resistance, adhesiveness, and process adhesiveness
are secured.
[0052] Although corrosion resistance, adhesiveness, and process adhesiveness are improved
as the amount of phosphate compound increases, if the amount of P contained in the
phosphate compound exceeds 100 mg/m
2 per one surface, the chemical treatment layer 107 becomes excessively thick, and
thus mainly due to a cohesive fracture, adhesiveness of the chemical treatment layer
107 to the Sn layer 105b deteriorates, electrical resistance increases, and thus weldability
is degraded. In addition, if the amount of P contained in the phosphate compound exceeds
100 mg/m
2, adhesion of the chemical treatment layer 107 becomes uneven, which may cause an
irregular appearance.
[0053] Thus, the amount of P contained in the phosphate compound in the chemical treatment
layer 107 according to the present embodiment is set to 1.0 to 100 mg/m
2 per one surface.
[0054] The amount of P contained in the phosphate compound in the chemical treatment layer
107 is preferably 2.0 to 70.0 mg/m
2 per one surface. By setting the amount of P contained in the phosphate compound in
the chemical treatment layer 107 to 2.0 mg/m
2 or more per one surface, more preferable sulfide stain resistance can be obtained.
In addition, by setting the amount of P contained in the phosphate compound of the
chemical treatment layer 107 to 70.0 mg/m
2 or less per one surface, the production costs of the chemical treatment layer 107
can be reduced further.
[0055] The chemical treatment layer 107 further contains the Al compound in addition to
the above-described Zr compound and phosphate compound. The Al compound of the chemical
treatment layer 107 exists mainly as Al oxide in the chemical treatment layer 107.
By reinforcing a film defect of the chemical treatment layer 107 having Zr as a main
component with the Al oxide, the chemical treatment steel sheet 10 can have excellent
sulfide stain resistance.
[0056] Since the chemical treatment layer 107 having Zr as a main component is inherently
a very uniform film, the amount of Al contained in the Al compound added to the chemical
treatment layer 107 to reinforce the film defect may be 0.10 mg/m
2 or more per one surface. By setting the amount of Al contained in the Al compound
to 0.10 mg/m
2 or more per one surface, sulfide stain resistance of the chemical treatment steel
sheet 10 can be satisfactorily improved.
[0057] Meanwhile, although sulfide stain resistance is improved when the amount of Al compound
in the chemical treatment layer 107 increases, if the amount of Al contained in the
Al compound exceeds 30.0 mg/m
2 per one surface, sulfide stain resistance is saturated, which is not economically
preferable. Thus, the amount of Al contained in the Al compound contained in the chemical
treatment layer 107 is set to 30.0 mg/m
2 or less per one surface.
[0058] The amount of Al contained in the Al compound in the chemical treatment layer 107
is more preferably 0.20 to 20.0 mg/m
2 per one surface. By setting the amount of Al containd in the Al compound to 0.20
mg/m
2 or more per one surface, sulfide stain resistance can be satisfactorily improved.
In addition, by setting the amount of Al contained in the Al compound to 20.0 mg/m
2 or less per one surface, the production costs of the chemical treatment layer 107
can be reduced further.
[0059] The amount of Al contained in the Al oxide (Al
2O
3) contained in the chemical treatment layer 107 is preferably 0.10 to 30.0 mg/m
2. When the amount of Al oxide contained in the chemical treatment layer 107 is within
the above-described range, a film defect of the chemical treatment layer 107 can be
satisfactorily reinforced and excellent sulfide stain resistance can be obtained.
[0060] In addition, by causing the Al compound to be contained in the chemical treatment
layer 107, the amount of phosphate compound for improving sulfide stain resistance,
like Al, can be reduced.
[0061] Phosphoric acid Zr included in the phosphate compound contained in the chemical treatment
layer 107, which is generated from reaction of phosphoric acid ions with Zr ions,
is precipitated when it exists in a large amount in a chemical treatment solution
for forming the chemical treatment layer 107, and the chemical treatment solution
becomes clouded.
[0062] Here, the Al compound contributes to improvement of sulfide stain resistance more
than the phosphate compound. Thus, since the chemical treatment layer 107 contains
the Al compound, the amount of phosphate compound, which is the cause of cloudiness
of the chemical conversion solution, can be reduced while satisfactorily improving
the sulfide stain resistance.
[0063] In addition, when the amount of phosphate compound is reduced, it is possible to
reduce an amount of F ions which inhibit the binding between Zr and phosphates and
the binding between Al and phosphates. As a result, since Zr is precipitated more
easily, it is possible to improve the electrolysis efficiency for forming the chemical
treatment layer 107.
[0064] Note that the chemical treatment layer 107 may contain inevitable impurities that
are incorporated thereinto during the production process or the like, in addition
to the above-described Zr compound, phosphate compound, and Al compound. In addition,
in a case where the chemical treatment layer 107 contains Cr, the upper limit of the
amount of Cr is 2 mg/m
2.
[0065] The chemical treatment steel sheet 10 according to the present embodiment exhibits
excellent sulfide stain resistance even if the adhered amount of the chemical treatment
layer 107 is reduced.
[0066] For example, a coating material may be applied to a surface of the chemical treatment
steel sheet 10, which is then baked, which results in forming a coating film. The
chemical treatment steel sheet 10 having the coating film formed on the surface is
placed to be fixed to the mouth of a heat resistant bottle holding 0.6 mass% of an
L-cysteine solution that has been boiled for one hour as a lid, and is subjected to
a heat treatment using a soaking furnace at 110°C for 30 minutes or the like. When
the appearance of the portion of the above-described heat-treated chemical treatment
steel sheet 10 in contact with the heat resistance bottle is observed, blackening
does not occur in 50% or more of the area of the contact portion in a case where the
chemical treatment steel sheet 10 according to the present embodiment is used.
[0067] As described above, the chemical treatment steel sheet 10 according to the present
embodiment has excellent corrosion resistance and sulfide stain resistance. Thus,
even in a case where the surface of the chemical treatment layer 107 is not covered
with a film or a coating material, the chemical treatment steel sheet 10 can be used
as a steel sheet for containers.
<Regarding layer structure of chemical treatment steel sheet 10>
[0068] The chemical treatment steel sheet 10 has the Fe-Sn alloy layer 105a, the Sn layer
105b, and the chemical treatment layer 107 on the steel sheet 103 as described above.
That is, in the chemical treatment steel sheet 10, the steel sheet 103 is in contact
with the Fe-Sn alloy layer 105a, and there is no other layer between the steel sheet
103 and the Fe-Sn alloy layer 105a. Likewise, the Fe-Sn alloy layer 105a is in contact
with the Sn layer 105b, and there is no other layer between the Fe-Sn alloy layer
105a and the Sn layer 105b. Furthermore, the Sn layer 105b is in contact with chemical
treatment layer 107, and there is no other layer between the Sn layer 105b and the
chemical treatment layer 107.
<Regarding measurement method for amount of component>
[0069] The amount of Sn and the amount of Fe contained in the Fe-Sn alloy layer 105a and
the Sn layer 105b can be measured using, for example, a fluorescent X-ray method.
In this case, using known samples for the amount of Sn or the amount of Fe, a calibration
curve for the amount of Sn or the amount of Fe is created in advance, and the amount
of Sn or the amount of Fe is determined relatively using the created calibration curve.
[0070] The amount of Zr, the amount of P, and the amount of Al contained in the chemical
treatment layer 107 can be measured using a quantitative analysis method, for example,
fluorescent X-ray analysis, or the like. In addition, which compounds exist in the
chemical treatment layer 107 can be specified by performing analysis using X-ray photoelectron
spectroscopy (XPS).
[0071] In addition, with regard to the amount of Al
2O
3 contained in the chemical treatment layer 107, a peak intensity ratio of Al
2O
3, Al metal, and other Al compound is first obtained using X-ray photoelectron spectroscopy
(XPS). Further, the amount of Al
2O
3 contained in the chemical treatment layer 107 is calculated on the basis of the total
Al metal amount obtained using the quantitative analysis method such as fluorescent
X-ray analysis and the peak intensity ratio obtained using XPS as described above.
[0072] Note that a measurement method for each component is not limited to the above-described
methods, and a known measurement method can be applied.
<Regarding method for manufacturing chemical treatment steel sheet>
[0073] Next, a method for manufacturing the chemical treatment steel sheet 10 according
to the present embodiment will be described in detail with reference to Fig. 2. Fig.
2 is a flowchart for describing an example of a flow of a method for manufacturing
the chemical treatment steel sheet 10 according to the present embodiment.
[Pre-treatment process]
[0074] In the method for manufacturing the chemical treatment steel sheet 10 according to
the present embodiment, first, known pre-treatment is performed on the steel sheet
103 if necessary (Step S101).
[Plating process]
[0075] Then, a Sn-plated layer (not shown) is formed on a surface of the steel sheet 103
(Step S103). A method for forming the Sn-plated layer (not shown) is not particularly
limited, and a known electroplating method, a method of immersing the steel sheet
103 in molten Sn, or the like can be used.
[Reflow treatment (reflow treatment process) process]
[0076] After the Sn-plated layer (not shown) is formed, reflow treatment (reflow treatment)
is performed (Step S104). Accordingly, the Fe-Sn alloy layer 105a and the Sn layer
105b are formed on the surface of the steel sheet 103.
[0077] The reflow treatment is performed by forming the Sn-plated layer (not shown) on the
steel sheet 103, then heating the steel sheet to a temperature of 200°C or higher
to melt the Sn-plated layer (not shown) temporarily, and then quenching the steel
sheet. Sn in the Sn-plated layer (not shown) located on the steel sheet 103 side is
alloyed with Fe contained in the steel sheet 103 through the reflow treatment, whereby
the Fe-Sn alloy layer 105a is formed, and the remaining Sn forms the Sn layer 105b.
[Electrolytic treatment process]
[0078] Then, the chemical treatment layer 107 is formed through cathodic electrolytic treatment
(Step S105).
[0079] The chemical treatment layer 107 is formed through electrolytic treatment (e.g.,
cathodic electrolytic treatment). A chemical treatment solution used to form the chemical
treatment layer 107 through electrolytic treatment contains 10 ppm or more and 20,000
ppm or less of Zr ions, 10 ppm or more and 20,000 ppm or less of F ions, 10 ppm or
more and 3,000 ppm or less of phosphate ions, 100 ppm or more and 30,000 ppm or less
of nitrate ions and sulfate ions in total, and 500 ppm or more and 5,000 ppm or less
of Al ions. In addition, (NH
4)
3AlF
6 is used as a supply source of Al ions in the chemical treatment solution.
[0080] Note that nitrate ions and sulfate ions may be contained at 10 ppm or more and 3,000
ppm or less in total of both ions in the chemical treatment solution, both ions of
nitrate ions and sulfate ions may be contained in the chemical treatment solution,
and only one of nitrate ions and sulfate ions may be contained in the chemical treatment
solution.
[0081] It is preferable for the chemical treatment solution to contain 200 ppm or more and
17,000 ppm or less of Zr ions, 200 ppm or more and 17,000 ppm or less of F ions, 100
ppm or more and 2,000 ppm or less of phosphate ions, 1,000 ppm or more and 23,000
ppm or less of nitrate ions and sulfate ions in total, and 500 ppm or more and 3,000
ppm or less of Al ions.
[0082] By setting the concentration of Zr ions to 200 ppm or more, it is possible to reliably
prevent a Zr adhered amount from decreasing. In addition, by setting the concentration
of F ions to 200 ppm or more, it is possible to more reliably prevent cloudiness of
the chemical treatment layer 107 accompanying with precipitation of phosphate.
[0083] Likewise, by setting the concentration of phosphate ions to 100 ppm or more, it is
possible to more reliably prevent cloudiness of the chemical treatment layer 107 accompanied
by precipitation of phosphate. In addition, by setting the concentration of nitrate
ions, or sulfate ions, or combination thereof to 1000 ppm or more, it is possible
to more reliably prevent adhesion efficiency of the chemical treatment layer 107 from
decreasing. In addition, by setting the concentration of Al ions to 500 ppm or more,
it is possible to realize the effect of improvement in sulfide stain resistance more
reliably.
[0084] Note that, by setting the upper limit value of each component of the chemical treatment
solution to the above-described values, the production costs of the chemical treatment
layer 107 can be reduced more reliably.
[0085] The temperature of the chemical treatment solution is preferably 5°C or higher and
lower than 90°C. In a case where the temperature of the chemical treatment solution
is lower than 5°C, it is not preferable because formation efficiency of the chemical
treatment layer 107 becomes poor, which is not economically efficient. In addition,
in a case where the temperature of the chemical treatment solution is 90°C or higher,
it is not preferable because a formed structure of the chemical treatment layer 107
becomes inhomogeneous and cracks, and defects such as micro cracks occur, and such
defects become a starting point of corrosion or the like.
[0086] Note that, when the temperature of the chemical treatment solution is higher than
the surface temperature of the steel sheet 103 on which the Fe-Sn alloy layer 105a
and the Sn layer 105b have been formed, reactivity of the chemical treatment solution
on the interface becomes higher, and thus adhesion efficiency of the chemical treatment
layer 107 is improved. Thus, it is preferable for the temperature of the chemical
treatment solution to be higher than the surface temperature of the steel sheet 103
on which the Fe-Sn alloy layer 105a and the Sn layer 105b have been formed.
[0087] The current density when electrolytic treatment is performed is preferably 1.0 A/dm
2 or higher and 100 A/dm
2 or lower. In a case where the current density is lower than 1.0 A/dm
2, the adhered amount of the chemical treatment layer 107 decreases, and an electrolytic
treatment time becomes long, which is not preferable. In addition, in a case where
the current density exceeds 100 A/dm
2, the adhered amount of the chemical treatment layer 107 becomes excessive, and it
is likely that a chemical treatment layer 107 with insufficient adhesion of the formed
chemical treatment layer 107 will be washed away (peeled off) in a cleaning process
by water-washing or the like after electrolytic treatment, which is not preferable.
[0088] A time for which electrolytic treatment is performed (electrolytic treatment time)
is preferably 0.20 seconds or longer and 150 seconds or shorter. In a case where the
electrolytic treatment time is shorter than 0.20 seconds, the adhered amount of the
chemical treatment layer 107 decreases and thus desired performance is not obtained,
which is not preferable. On the other hand, in a case where the electrolytic treatment
time exceeds 150 seconds, the adhered amount of the chemical treatment layer 107 becomes
excessive, and thus it is likely that a chemical treatment layer 107 with insufficient
adhesion of the formed chemical treatment layer 107 is washed away (peeled off) in
the cleaning process by water-washing or the like after electrolytic treatment, which
is not preferable.
[0089] The pH of the chemical treatment solution is preferably in the range of 3.1 to 3.7,
and more preferably about 3.5. Nitric acid, ammonia, or the like may be added to adjust
the pH of the chemical treatment solution if necessary.
[0090] By performing electrolytic treatment under the above-described conditions, the chemical
treatment layer 107 according to the present embodiment can be formed on a surface
of the Sn layer 105b.
[0091] In forming the chemical treatment layer 107 according to the present embodiment,
tannic acid may be further added to the chemical treatment solution to be used in
electrolytic treatment. By adding tannic acid to the chemical treatment solution,
tannic acid reacts with Fe contained in the steel sheet 103, and a film of iron tannate
is formed on the surface of the steel sheet 103. The film of iron tannate is preferable
because it improves corrosion resistance and adhesiveness.
[0092] As a solvent of the chemical treatment solution, for example, deionized water, distilled
water, or the like can be used. A preferable electric conductivity of the solvent
of the chemical treatment solution is 10 µS/cm or lower, more preferably 5 µS/cm or
lower, and more preferably 3 µS/cm or lower. However, a solvent of the chemical treatment
solution is not limited thereto, and one can be appropriately selected depending on
materials to be dissolved, formation methods, formation conditions of the chemical
treatment layer 107, and the like. However, it is preferable to use deionized water
or distilled water in light of industrial productivity, costs, and the environment
based on stability of the adhered amount of each stable component.
[0093] As a supply source of Zr, for example, a Zr complex such as H
2ZrF
6 can be used. Zr in the above-described Zr complex exists as Zr
4+ in the chemical treatment solution due to a hydrolysis reaction accompanying with
an increase of the pH on a cathode electrode interface. Zr ions thereof is subjected
to a dehydration condensation reaction with hydroxyl groups (-OH) existing on a metal
surface in the chemical treatment solution, and thereby a compound such as ZrO
2 or Zr
3(PO
4)
4 is formed.
[0094] In addition, in the chemical treatment solution, (NH
4)
3AlF
6 is used as a supply source of Al. By using (NH
4)
3AlF
6 as a supply source of Al, Al exists in the chemical treatment solution in a state
in which Al forms a complex with F (which will be referred to as an AlF complex).
Since Al included in the AlF complex is precipitated together with Zr in the electrolytic
treatment process and is included in the chemical treatment layer 107, it contributes
to sulfide stain resistance as described above.
[0095] In addition, Al exists in the chemical treatment solution as cations, like Zr. Thus,
by using (NH
4)
3AlF
6 as a supply source of Al, Al can be supplied to the chemical treatment solution,
without increasing the concentration of phosphate ions.
[0096] Meanwhile, in a case where Al
2(SO
4)
3 or the like is used as a supply source of Al as disclosed in Patent Document 3, no
AlF complex is formed, thus Al is not satisfactorily precipitated in the electrolytic
treatment process, and the amount of Al contained in the chemical treatment layer
107 becomes very small. In this case, the chemical treatment layer 107 does not have
satisfactory sulfide stain resistance, which is not preferable.
[Post-treatment process]
[0097] Then, known post-treatment is performed on the steel sheet 103 on which the Fe-Sn
alloy layer 105a, the Sn layer 105b, and the chemical treatment layer 107 have been
formed, if necessary (Step S107).
[0098] By performing the treatment in the above-described flow, the chemical treatment steel
sheet 10 according to the present embodiment is produced.
[0099] Note that, although the case where the chemical treatment layer 107 is formed through
electrolytic treatment has been described above, in a case where a sufficient time
can be allowed to form a chemical conversion coated film, the chemical treatment layer
107 may be formed through immersion treatment, rather than electrolytic treatment.
[Examples]
[0100] The chemical treatment steel sheet and the method for manufacturing a chemical treatment
steel sheet according to an embodiment of the present invention will be described
in detail below with introduction of examples. Note that the examples introduced below
are merely examples of the chemical treatment steel sheet and the method for manufacturing
a chemical treatment steel sheet according to an embodiment of the present invention,
and the chemical treatment steel sheet and the method for manufacturing a chemical
treatment steel sheet according to an embodiment of the present invention are not
limited to the following examples.
(Example 1)
[0101] In Example 1, how sulfide stain resistance changes was examined by changing the amount
of Al compound, without changing the amounts of Zr compound and phosphate compound
in chemical treatment layers.
[0102] In Example 1, steel sheets that are generally used as steel sheets for containers
were used as a base material. Fe-Sn alloy layers and Sn layers were formed on the
steel sheets by performing reflow treatment in a state in which Sn-plated layers were
formed on the steel sheets. The total amount of Sn contained in the Fe-Sn alloy layer
and the Sn layer was set to 2.8 g/m
2 per one surface for all samples.
[0103] Further, chemical treatment layers were formed by changing the concentration of Al
compounds in the chemical treatment layers of each sample, and thereby a plurality
of samples were produced. Here, the amount of Zr contained in the Zr compound in each
sample was 8 mg/m
2 per one surface, and the amount of P contained in the phosphate compound was 3 mg/m
2 per one surface.
[0104] Evaluation of sulfide stain resistance was made as follows. First, 0.6 mass% of L-cysteine
solution that has been boiled for one hour was put into heat resistant bottles, and
the above-described samples (ϕ40 mm) were placed on and fixed to the mouths of the
heat resistant bottles as lids. Next, the heat resistant bottles with the lids placed
thereon as described above were subjected to heat treatment (retort treatment) in
soaking furnace at 110°C for 15 minutes. Thereafter, for each sample, the appearance
of the portion in contact with the heat-resistant bottle was observed and evaluated
according to 10 levels based on the following criteria. In the following evaluation
criteria, actual use could be withstood if a score was 5 points or more.
<Evaluation criteria for sulfide stain resistance>
[0105] Ratios of the areas that did not change to black to the contact areas of the samples
with the 0.6 mass% of L-cysteine solution were graded by scores from 1 point to 10
points.
10 points: 90% or higher and less than or equal to 100%
9 points: 80% or higher and less than 90%
8 points: 70% or higher and less than 80%
7 points: 60% or higher and less than 70%
6 points: 50% or higher and less than 60%
5 points: 40% or higher and less than 50%
4 points: 30% or higher and less than 40%
3 points: 20% or higher and less than 30%
2 points: 10% or higher and less than 20%
1 point: 0% or higher and less than 10%
[0106] The obtained evaluation results are shown in Fig. 3. In Fig. 3, the horizontal axis
represents the amount of Al compound (amount of Al metal) in the chemical treatment
layer included in each sample, and the vertical axis represents the evaluation results
of sulfide stain resistance.
[0107] As shown in Fig. 3, the score of the evaluation result of sulfide stain resistance
was 1 point in the case where the amount of Al contained in the Al compound was less
than 0.10 mg/m
2 per one surface. On the other hand, the score of the evaluation result of sulfide
stain resistance was 7 points or higher in the case where the amount of Al contained
in the Al compound was 0.10 mg/m
2 or more per one surface, and therefore it was clarified that the samples had extremely
excellent sulfide stain resistance.
[0108] The results demonstrate that sulfide stain resistance of the chemical treatment steel
sheet having the chemical treatment film is dramatically improved by causing the chemical
treatment layer to contain a predetermined amount of Al compound.
(Example 2)
[0109] Next, how sulfide stain resistance changes while the amount of each component contained
in each chemical treatment layer 107 is changed was examined.
[0110] More specifically, chemical treatment layers were formed on Sn layers using steel
sheets on which Fe-Sn alloy layers and the Sn layers had been formed.
[0111] In addition, chemical treatment layers were formed using Al
2(SO
4)
3 as a supply source of Al ions in Comparative Examples a5 and a6 while (NH
4)
3AlF
6 was used as a supply source of Al ions in Invention Examples A1 to A18 and Comparative
Examples a1 to a4.
[0112] With respect to the chemical treatment steel sheets of Al to A18 and a1 to a6, the
amounts of Zr, P, and Al contained in the chemical treatment layers were measured
using a fluorescent X-ray adhesion meter, and then corrosion resistance and sulfide
stain resistance thereof were evaluated.
[0113] In addition, for the amount of Al
2O
3 contained in the chemical treatment layers, peak intensity ratios of Al
2O
3, Al metal, and other Al compounds were first obtained using X-ray photoelectron spectroscopy
(XPS). Further, the amount of Al
2O
3 contained in the chemical treatment layers was calculated using the total amount
of Al metal obtained using a quantitative analysis method such as fluorescent X-ray
analysis and the peak intensity ratios obtained through XPS as described above.
<Evaluation of corrosion resistance>
[0114] 3% acetic acid was used as a corrosion resistance test solution. The chemical treatment
steel sheets serving as samples were cut out to ϕ35 mm, and then placed on and fixed
to the mouths of heat resistant bottles each containing the corrosion resistance test
solutions. After having the samples subjected to heat treatment at 121°C for 60 minutes,
the portions of the samples in contact with the corrosion resistance test solutions
were observed to evaluate the degrees of corrosion of the samples. Specifically, evaluation
was made in 10 levels as follows for ratios of the areas with no corrosion to the
contact areas of the samples with the corrosion resistance test solutions. Note that,
if the score is 5 points or higher, the samples can be used as steel sheets for containers.
[0115]
10 points: 90% or higher and less than or equal to 100%
9 points: 80% or higher and less than 90%
8 points: 70% or higher and less than 80%
7 points: 60% or higher and less than 70%
6 points: 50% or higher and less than 60%
5 points: 40% or higher and less than 50%
4 points: 30% or higher and less than 40%
3 points: 20% or higher and less than 30%
2 points: 10% or higher and less than 20%
1 point: 0% or higher and less than 10%
[0116] For the items of corrosion resistance evaluation, 10 points to 9 points are marked
as "very good," 8 points to 5 points are marked as "good," and 4 points or lower are
marked as "not good."
<Evaluation of sulfide stain resistance>
[0117] Evaluation of sulfide stain resistance was made as follows. 0.6 mass% of L-cysteine
solution that had been boiled for one hour was put into heat resistant bottles, and
the above-described samples (ϕ40 mm) were placed on and fixed to the mouths of the
heat resistant bottles as lids. The heat resistant bottles with the lids placed thereon
as described above underwent heat treatment (retort treatment) in a soaking furnace
at 110°C for 15 minutes. Then, the appearances of the portions of the respective samples
in contact with the heat resistant bottles were observed, and evaluation was made
in 10 levels on the basis of the same criteria as above. In Table 1 shown below, 10
points to 8 points are marked as "very good," 7 points to 5 points are marked as "good,"
and 4 points and lower are marked as "not good."
[0118] The obtained results are shown in the following Table 1.
[Table 1]
|
Symbol |
Chemical Treatment Steel Sheet |
Corrosion Resistance |
Sulfur Stain Resistance |
Plated layer |
Chemical treatment layer |
Amount of Sn as Sn metal (g/m2) |
Amount of Zr as Zr metal (mg/m2) |
Amount of P (mg/m2) |
Total amount of Al (mg/m2) |
Amount of Al in Al2O3 (mg/m2) |
|
A1 |
0.12 |
143 |
77 |
5.2 |
3.0 |
Good |
Very Good |
|
A2 |
29 |
128 |
9.1 |
16 |
8.0 |
Very Good |
Very Good |
|
A3 |
15 |
1.2 |
29 |
29 |
13 |
Very Good |
Good |
|
A4 |
26 |
149 |
2.4 |
2.8 |
1.7 |
Very Good |
Very Good |
|
A5 |
21 |
23 |
1.1 |
25 |
22 |
Very Good |
Good |
|
A6 |
27 |
7.1 |
98 |
2.3 |
1.0 |
Very Good |
Very Good |
|
A7 |
14 |
66 |
54 |
0.12 |
0.11 |
Very Good |
Good |
|
A8 |
10 |
108 |
59 |
29 |
28 |
Very Good |
Very Good |
Invention |
A9 |
27 |
1.2 |
59 |
26 |
14 |
Very Good |
Very Good |
Example |
A10 |
6.6 |
118 |
72 |
25 |
14 |
Very Good |
Very Good |
|
A11 |
7.7 |
112 |
2.3 |
2.5 |
2.1 |
Very Good |
Very Good |
|
A12 |
0.3 |
33 |
68 |
13 |
10 |
Very Good |
Very Good |
|
A13 |
23 |
36 |
79 |
0.2 |
0.13 |
Very Good |
Very Good |
|
A14 |
15 |
142 |
92 |
19 |
18 |
Very Good |
Very Good |
|
A15 |
0.3 |
80 |
90 |
0.6 |
0.3 |
Very Good |
Very Good |
|
A16 |
18 |
2.9 |
68 |
27 |
17 |
Very Good |
Very Good |
|
A17 |
2.6 |
14 |
5.3 |
3.2 |
2.3 |
Very Good |
Very Good |
|
A18 |
5.2 |
23 |
8.3 |
2.1 |
1.5 |
Very Good |
Very Good |
Comparative Example |
a1 |
0.05 |
143 |
142 |
10 |
4.9 |
Not Good |
Very Good |
|
a2 |
12 |
0.04 |
53 |
35 |
17 |
Not Good |
Very Good |
a3 |
35 |
138 |
0.3 |
5.8 |
3.4 |
Very Good |
Not Good |
a4 |
12 |
182 |
35 |
0.06 |
0.03 |
Very Good |
Not Good |
a5 |
23 |
2 |
3 |
0.03 |
0.02 |
Very Good |
Not Good |
a6 |
0.5 |
43 |
12 |
0.04 |
0.03 |
Very Good |
Not Good |
[0119] As is obvious from Table 1, Examples A1 to A18 all had excellent corrosion resistance
and excellent sulfide stain resistance. On the other hand, Comparative Examples a1
to a6 exhibited either of inferior corrosion resistance or inferior sulfide stain
resistance. Note that, in Comparative Examples a5 and a6 in which Al
2(SO
4)
3 was used as a supply source of Al ions, the amounts of Al and Al
2O
3 were significantly small, and sulfide stain resistance was "not good."
(Example 3)
[0120] Next, how sulfide stain resistance changes according to the amount of Sn and the
amount of each component contained in chemical treatment layers was examined.
[0121] The amount of S in each of the samples is shown in Table 2, and conditions for chemical
treatment (conditions for chemical treatment solutions and conditions for electrolytic
treatment) are shown in Table 3. The amounts of Zr, P, Al, and Al
2O
3 contained in the chemical treatment layers formed in each of the samples are shown
in Table 4.
[0122] In addition, corrosion resistance and sulfide stain resistance were evaluated for
each of the samples as in Example 2. The results are shown in Table 4.
[0123] Note that the chemical treatment layers were formed using Al
2(SO
4)
3 as a supply source of Al ions in Comparative Examples b9 and b10 while (NH
4)
3AlF
6 was used as a supply source of Al ions in Invention Examples B1 to B31 and Comparative
Examples b1 to b8.
[Table 2]
|
Symbol |
Plated Layer |
|
|
Amount of Sn as Sn metal (g/m2) |
|
B1 |
17 |
|
B2 |
21 |
|
B3 |
14 |
|
B4 |
10 |
|
B5 |
13 |
|
B6 |
21 |
|
B7 |
9.2 |
|
B8 |
27 |
|
B9 |
5.0 |
|
B10 |
12 |
|
B11 |
28 |
|
B12 |
10 |
|
B13 |
24 |
|
B14 |
19 |
|
B15 |
27 |
Invention Example |
B16 |
4.3 |
|
B17 |
3.8 |
|
B18 |
27 |
|
B19 |
22 |
|
B20 |
1.7 |
|
B21 |
22 |
|
B22 |
11 |
|
B23 |
18 |
|
B24 |
26 |
|
B25 |
8.1 |
|
B26 |
28 |
|
B27 |
24 |
|
B28 |
12 |
|
B29 |
3.4 |
|
B30 |
0.8 |
|
B31 |
19 |
Comparative Example |
b1 |
5.1 |
b2 |
0.6 |
b3 |
21 |
b4 |
7.1 |
b5 |
21 |
b6 |
8.4 |
b7 |
11 |
b8 |
17 |
b9 |
21 |
b10 |
17 |
[Table 3]
|
Symbol |
Chemical treatment |
Chemical treatment bath |
Electrolytic treatment |
Zr ions (ppm) |
F ions (ppm) |
Phosphate ions (ppm) |
Nitrate ions (ppm) |
Sulfate ions (ppm) |
Al ions (ppm) |
Supply source of Al ions |
Bath temperature (°C) |
Current (A/dm2) |
Time (sec) |
|
B1 |
12 |
19683 |
1596 |
5328 |
11630 |
4447 |
(NH4)3AlF6 |
25 |
7 |
115 |
|
B2 |
19857 |
16417 |
2085 |
2638 |
12852 |
699 |
(NH4)3AlF6 |
22 |
67 |
72 |
|
B3 |
5092 |
11 |
535 |
6859 |
18519 |
4925 |
(NH4)3AlF6 |
82 |
28 |
47 |
|
B4 |
704 |
19347 |
514 |
9817 |
4173 |
4451 |
(NH4)3AlF6 |
40 |
15 |
24 |
|
B5 |
2341 |
5154 |
12 |
14898 |
5773 |
4354 |
(NH4)3AlF6 |
77 |
73 |
96 |
|
B6 |
13494 |
16380 |
2945 |
21524 |
1923 |
4802 |
(NH4)3AlF6 |
19 |
22 |
124 |
|
B7 |
6419 |
8852 |
2058 |
111 |
- |
2949 |
(NH4)3AlF6 |
67 |
11 |
134 |
|
B8 |
7489 |
15872 |
1548 |
26374 |
- |
2328 |
(NH4)3AlF6 |
21 |
24 |
127 |
|
B9 |
16214 |
9235 |
1369 |
- |
103 |
2334 |
(NH4)3AlF6 |
45 |
82 |
2 |
Invention |
B10 |
1348 |
13442 |
1592 |
- |
29834 |
3564 |
(NH4)3AlF6 |
67 |
16 |
47 |
Example |
B11 |
4254 |
4545 |
2124 |
17330 |
8589 |
512 |
(NH4)3AlF6 |
28 |
67 |
32 |
|
B12 |
8364 |
19302 |
1584 |
7806 |
21587 |
4983 |
(NH4)3AlF6 |
44 |
54 |
114 |
|
B13 |
3600 |
17014 |
2229 |
244 |
22137 |
2573 |
(NH4)3AlF6 |
5.2 |
82 |
66 |
|
B14 |
3567 |
2061 |
1208 |
9103 |
5683 |
4094 |
(NH4)3AlF6 |
89 |
64 |
51 |
|
B15 |
5914 |
15314 |
2055 |
3400 |
8852 |
3626 |
(NH4)3AlF6 |
19 |
1.2 |
130 |
|
B16 |
12026 |
17033 |
2493 |
18941 |
2356 |
2356 |
(NH4)3AlF6 |
46 |
97 |
144 |
|
B17 |
12626 |
5608 |
1146 |
3103 |
23543 |
612 |
(NH4)3AlF6 |
66 |
72 |
0.3 |
|
B18 |
14698 |
10301 |
1237 |
766 |
18229 |
4209 |
(NH4)3AlF6 |
17 |
22 |
148 |
|
B19 |
211 |
6192 |
2522 |
9202 |
4542 |
2679 |
(NH4)3AlF6 |
85 |
99 |
21 |
|
B20 |
16834 |
12796 |
1552 |
18544 |
7240 |
866 |
(NH4)3AlF6 |
82 |
18 |
122 |
|
B21 |
18497 |
204 |
292 |
14641 |
7805 |
1490 |
(NH4)3AlF6 |
10 |
52 |
96 |
B22 |
19980 |
16732 |
879 |
10894 |
18808 |
3949 |
(NH4)3AlF6 |
50 |
67 |
15 |
B23 |
7370 |
14400 |
104 |
18583 |
5778 |
951 |
(NH4)3AlF6 |
85 |
51 |
41 |
B24 |
14865 |
19570 |
2780 |
4729 |
9162 |
2954 |
(NH4)3AlF6 |
49 |
75 |
31 |
B25 |
13324 |
5902 |
755 |
973 |
72 |
1525 |
(NH4)3AlF6 |
14 |
16 |
63 |
B26 |
2470 |
8351 |
240 |
22873 |
56 |
3618 |
(NH4)3AlF6 |
41 |
46 |
107 |
B27 |
1111 |
178 |
2985 |
91 |
983 |
562 |
(NH4)3AlF6 |
47 |
96 |
81 |
B28 |
6655 |
9712 |
2770 |
115 |
22384 |
554 |
(NH4)3AlF6 |
68 |
4 |
50 |
B29 |
4205 |
192 |
2849 |
4072 |
812 |
2984 |
(NH4)3AlF6 |
78 |
67 |
133 |
B30 |
8136 |
17766 |
2984 |
2420 |
15290 |
4618 |
(NH4)3AlF6 |
78 |
34 |
87 |
B31 |
9377 |
16433 |
136 |
5889 |
6644 |
4129 |
(NH4)3AlF6 |
32 |
83 |
103 |
Comparative Example |
b1 |
2 |
4 |
2315 |
30392 |
30302 |
4646 |
(NH4)3AlF6 |
7 |
39 |
31 |
b2 |
39584 |
35393 |
6843 |
2467 |
4417 |
833 |
(NH4)3AlF6 |
36 |
100 |
68 |
b3 |
18608 |
4938 |
4 |
9843 |
9868 |
3837 |
(NH4)3AlF6 |
14 |
70 |
94 |
b4 |
11174 |
9218 |
2538 |
69 |
12 |
2734 |
(NH4)3AlF6 |
38 |
89 |
57 |
b5 |
11586 |
16949 |
716 |
2018 |
6326 |
120 |
(NH4)3AlF6 |
98 |
71 |
103 |
b6 |
12729 |
227 |
2910 |
17217 |
276 |
2456 |
(NH4)3AlF6 |
3 |
129 |
130 |
b7 |
15053 |
19771 |
1546 |
6903 |
20580 |
848 |
(NH4)3AlF6 |
19 |
0.7 |
187 |
b8 |
12839 |
13209 |
2905 |
539 |
4706 |
4177 |
(NH4)3AlF6 |
36 |
6 |
0.1 |
b9 |
19283 |
2004 |
1837 |
2932 |
523 |
3465 |
Al2(SO4)3 |
15 |
12 |
34 |
b10 |
3829 |
3283 |
1232 |
23533 |
6545 |
624 |
Al2(SO4)3 |
25 |
2 |
24 |
[Table 4]
|
Symbol |
Chemical treatment layer |
Corrosion Resistance |
Sulfur Stain Resistance |
Amount of Zr as Zr metal (mg/m2) |
Amount of P (mg/m2) |
Total amount of Al (mg/m2) |
Amount of Al in Al2O3 (mg/m2) |
Invention |
B1 |
8.1 |
3.5 |
1.5 |
0.9 |
Very Good |
Good |
Example |
B2 |
48 |
18 |
8.1 |
7.0 |
Very Good |
Very Good |
|
B3 |
13 |
5.6 |
2.4 |
1.2 |
Very Good |
Very Good |
|
B4 |
3.6 |
1.4 |
0.6 |
0.3 |
Very Good |
Good |
|
B5 |
59 |
27 |
13 |
10 |
Very Good |
Good |
|
B6 |
23 |
11 |
4.9 |
3.9 |
Very Good |
Very Good |
|
B7 |
15 |
6.2 |
2.5 |
1.8 |
Very Good |
Good |
|
B8 |
29 |
11 |
4.8 |
2.1 |
Very Good |
Very Good |
|
B9 |
1.1 |
1.2 |
0.6 |
0.2 |
Very Good |
Good |
|
B10 |
6.2 |
2.9 |
1.2 |
1.1 |
Very Good |
Very Good |
|
B11 |
19 |
8.4 |
3.5 |
2.8 |
Very Good |
Good |
|
B12 |
53 |
22 |
12 |
5.1 |
Very Good |
Very Good |
|
B13 |
49 |
23 |
9.4 |
7.8 |
Very Good |
Good |
|
B14 |
30 |
14 |
6.6 |
4.8 |
Very Good |
Very Good |
|
B15 |
1.4 |
1.4 |
0.3 |
0.12 |
Very Good |
Good |
|
B16 |
132 |
53 |
26 |
21 |
Very Good |
Very Good |
|
B17 |
1.2 |
3.2 |
0.3 |
0.2 |
Very Good |
Good |
|
B18 |
27 |
14 |
5.4 |
4.6 |
Very Good |
Very Good |
|
B19 |
20 |
8.1 |
3.8 |
2.8 |
Very Good |
Very Good |
|
B20 |
20 |
8.3 |
3.6 |
2.9 |
Very Good |
Very Good |
|
B21 |
40 |
21 |
8.3 |
5.1 |
Very Good |
Very Good |
|
B22 |
10 |
3.9 |
1.8 |
1.2 |
Very Good |
Very Good |
|
B23 |
18 |
7.5 |
4.0 |
2.0 |
Very Good |
Very Good |
|
B24 |
21 |
10 |
3.9 |
2.0 |
Very Good |
Very Good |
|
B25 |
9.1 |
3.7 |
1.8 |
1.3 |
Very Good |
Very Good |
|
B26 |
48 |
21 |
8.9 |
4.3 |
Very Good |
Very Good |
|
B27 |
76 |
31 |
15 |
12 |
Very Good |
Very Good |
|
B28 |
1.7 |
2.1 |
0.3 |
0.2 |
Very Good |
Very Good |
|
B29 |
77 |
33 |
16 |
11 |
Very Good |
Very Good |
|
B30 |
27 |
11 |
5.3 |
2.6 |
Very Good |
Very Good |
|
B31 |
74 |
33 |
16 |
7.8 |
Very Good |
Very Good |
Comparative Example |
b1 |
0.6 |
6.7 |
2.3 |
2.1 |
Very Good |
Not Good |
b2 |
0.3 |
14 |
13 |
8.7 |
Very Good |
Not Good |
b3 |
56 |
0.6 |
12 |
9.9 |
Very Good |
Not Good |
b4 |
0.3 |
33 |
8.1 |
5.9 |
Very Good |
Not Good |
b5 |
59 |
2.1 |
0.03 |
0.02 |
Very Good |
Not Good |
b6 |
0.4 |
3.2 |
4.7 |
3.1 |
Very Good |
Not Good |
b7 |
0.4 |
1.2 |
0.2 |
0.15 |
Very Good |
Not Good |
b8 |
0.1 |
1.5 |
0.4 |
0.2 |
Very Good |
Not Good |
b9 |
12 |
1.3 |
0.03 |
0.02 |
Very Good |
Not Good |
|
13 |
1.3 |
0.04 |
0.03 |
Very Good |
Not Good |
[0124] As shown in Table 4, the present invention examples B1 to B31 produced in the method
for manufacturing the chemical treatment steel sheets according to the present embodiment
all had excellent corrosion resistance and sulfide stain resistance. Meanwhile, while
Comparative Examples b1 to b10 all exhibited excellent corrosion resistance, sulfide
stain resistance was poor. Note that, in Comparative Examples b9 and b10 in which
Al
2(SO
4)
3 was used as a supply source of Al ions, the amounts of Al and Al
2O
3 were significantly small, and sulfide stain resistance was also "not good."
[0125] Although exemplary embodiments of the present invention have been described above
in detail with reference to the appended drawings, the present invention is not limited
thereto. It is obvious that a person having general knowledge in the field of the
technology to which the present invention belongs can conceive various modified examples
or corrected examples in the scope of the technical gist described in the claims,
and it is of course understood that the examples belong to the technical scope of
the present invention.
[Field of Industrial Application]
[0126] According to an embodiment described above, even in a case where an adhered amount
of a chemical treatment layer is small, a chemical treatment steel sheet having excellent
corrosion resistance and sulfide stain resistance and a method for manufacturing a
chemical treatment steel sheet can be provided.
[Brief Description of the Reference Symbols]
[0127]
10 chemical treatment steel sheet
103 Steel sheet
105a Fe-Sn alloy layer
105b Sn layer
107 chemical treatment layer