Background of the Invention
Field of the Invention:
[0001] The present invention relates to a seamless can obtained by deeply drawing a steel
plate having an organic coating and to a method of producing the same. More particularly,
the present invention relates to a deeply drawn corrosion-resistant can made of a
laminated material of a metal substrate having a tin-containing metal that is coated
at a rate that lies within a predetermined range and an organic coating layer, the
can being suited for containing acidic beverages and sport beverages, and to a method
of producing the same can.
Prior Art:
[0002] Side-seamless can have heretofore been produced by subjecting a metal material such
as an aluminum plate, a tin plate or a tin-free steel plate to the drawing of at least
one stage between a drawing die and a punch to form a cup which consists of a drum
portion with no seam on the side surface thereof and a bottom portion connected integrally
to the drum portion without forming seam, and then, as required, squeezing the drum
portion between a drawing punch and a squeezing die in order to reduce the thickness
of the drum portion of the can. It has also been known to produce the side-seamless
cans by using a material obtained by laminating a thermoplastic resin film such as
a polypropylene of a thermoplastic polyester on the metal material.
[0003] Japanese Patent Publication Laid-Open No. 258822/1989 filed by the present inventors
discloses a method of reducing the thickness of side walls of cans by effecting the
bend-stretching at the time of the deep drawing, i.e., discloses a redrawing method
wherein a predrawn cup of a coated metal plate is held by an annular holding member
inserted in the cup and a redrawing die, a redrawing punch and the redrawing die are
moved relative to each other in mesh with each other, the redrawing punch and the
redrawing die being provided in concentric with the holding member and the redrawing
die so as to be inserted in or come out from the holding member, thereby to form a
deeply drawn cup having a diameter smaller than that of the predrawn cup, and wherein
the radium curvature (RD) of the action corner of the redrawing die is 1 to 2.9 times
as great as the thickness (tB) of the metal plate, the radius of curvature (RD) of
the holding corner of the holding member is 4.1 to 12 times as great as the thickness
(tB) of the metal plate, the plane engaging portions of the holding member and the
redrawing die that engage with the predrawn cup have a dynamic coefficient of friction
of 0.001 to 0.2, at least one stage of drawing is effected so that the redrawing ration
defined as a ratio of the diameter of a shallowly drawn cup to the diameter of a deeply
drawn cup lies over a range of 1.1 to 1.5, the whole side wall of the cup is uniformly
bent in the direction of the height in order to reduce the thickness. It has also
been proposed to use a tin-free steel (TFS: steel plate electrolytically treated with
chromic acid) as a coated metal plate.
[0004] A material of cans consisting of TFS as a base material coated with an organic resin
allows a resin coating layer to be intimately adhered thereto, and does not develop
such a problem that the resin coating material is peeled off during the deep drawing
or while the thickness is being as a result of drawing, during the neck-in treatment,
double seaming relative to the cover, heat-sterilization treatment, or while the contents
are being preserved. Therefore, the deeply drawn can made of such a material exhibit
excellent processing properties.
[0005] In mass-producing the cans, however, defects and damages by the treatment may often
develop in the organic resin coating material at a predetermined frequency permitting,
sometimes, the underlying metal to be exposed. The coating on the TFS surface has
a limited resistance against corrosion. Therefore, if the underlying metal is exposed,
iron is abnormally eluted out or holes are formed resulting in the leakage when there
are contained acidic beverages and spots beverages that cause the steel plate to be
vigorously corroded.
[0006] In order to cope with the above problem, it can be contrived to treat the surface
of the steel plate with tin or a tin alloy which exhibits corrosion-preventing effect
that stems from the sacrificial dissolution of tin in order to impart corrosion-resistant
property to the surface coating of the steel plate.
[0007] With the presently available tin-plated steel plates, however, intimacy or adhesiveness
to the organic resin coating material is exhibited to a degree which is just enough
to withstand a light degree of processing such as shallow drawing, but is not exhibited
to a degree large enough to withsand the deep drawing and the subsequent neck-in processing
and double lap-seaming.
Summary of the Invention
[0008] The object of the present invention therefore is to provide a deeply drawn can having
excellent corrosion resistance which is capable of containing acidic beverages or
sports beverages having large corrosion-promoting property and which can be deeply
drawn or can be subjected to the treatment for reducing the thickness.
[0009] According to the present invention, there is provided a deeply drawn can having excellent
corrosion resistance made of a laminated material which comprises:
a metal substrate having a steel plate, a tin-containing metal applied thereon
at a coating rate defined by the formula,

wherein VFe represents a photoelectric intensity of iron at a moment when the
photoelectric intensity of iron (Fe) and the photoelectric intensity of tin (Sn) have
entered into nearly a steady state while subjecting the surface of the steel plate
to be coated an X-ray photoelectric spectroscopic method to etch the surface of said
steel plate, and VFeo represents a photoelectric intensity of iron at a moment when
the etching is further carried out and the photoelectric intensity of tin (Sn) becomes
substantially zero,
of 20 to 80%, metal chromium and a hydrated chromium oxide which are applied onto
the whole surface of the steel plate coated with the tin-containing metal; and
an organic resin coating applied onto the surface of said metal substrate.
[0010] In the material of cans used in the present invention, the tin-containing metal layer
should be homogeneously and uniformed distributed on the steel plate substrate as
a plated layer having a sea-island relationship with an average size in the plane
direction of from 0.1 to 10 µm and, particularly, 0.2 to 5 µm. Further, the tin-containing
metal layer should contain tin in an amount of greater than 20%, and should be in
the form of a tin-plated layer, a tin-iron alloy layer, or a tin nickel-plated layer.
[0011] According to the present invention, furthermore, there is provided a redrawing method
wherein the laminated member is drawn into a shallow predrawn cup, said predrawn cup
is held by an annular holding member inserted in said cup and by a redrawing die,
a redrawing punch and the redrawing die are moved relative to each other and in mesh
with each other, said redrawing punch and said redrawing die being provided in concentric
with said holding member and said redrawing die so as to move into and come out of
the holding member, in order to form a deeply drawn cup having a diameter smaller
than that of said predrawn cup, and the whole side wall of the cup is uniformly bent
in the direction of the height to decrease the thickness of the side wall of the cup.
[0012] According to the method of the present invention, the radius of curvature (RD) of
the action corner of the redrawing die is 1 to 2.9 times as great as the thickness
(tB) of the metal plate, the radius of curvature (RD) of the holding corner of the
holding member is 4.1 to 12 times as great as the thickness (tB) of the metal plate,
the plane engaging portions of the holding member and the redrawing die that engage
with the predrawn cup have a dynamic coefficient of friction of 0.001 to 0.2, and
at least one stage of draw-molding is effected so that a redrawing ratio defined as
a ratio of the diameter of the shallowly drawn cup to the diameter of the deeply drawn
cup lies over a range of from 1.1 to 1.5.
[0013] A distinguished feature of the present invention is that the tin-containing metal
is not applied as a completely continuous coating onto the steel plate substrate,
but is applied in such a manner that the surfaces of the tin-containing metal and
the steel surfaces exist being mixed together on the surface of the steel plate substrate,
and that metal chromium and a surface-treated layer of a chromium oxide are formed
on the above surface that is incompletely coated with the tin-containing metal. This
makes it possible to greatly increase the corrosion resistance of the metal substrate
itself as well as to greatly improve the adhesiveness between the metal substrate
and the organic resin coating material to be capable of withstanding severe deep drawing
and the reduction of thickness by bending and stretching the side walls.
[0014] Usually, the distribution of atoms on the metal substrate and the chemical composition
can be measured by the X-ray photoelectric spectroscopic method. In the present invention,
satisfactory results are obtained when the coating rate of the above-mentioned equation
(1) lies from 20 to 80% and, preferably, from 30 to 60% as measured by the photoelectric
spectroscopic method.
[0015] Fig. 1 shows the measure results of the metal substrate used in the present invention
by the X-ray photoelectric spectroscopic method, wherein the abscissa represents the
treatment time of when the steel plate is sputtered with argon ions. The sputtering
for about 20 minutes corresponds to the etching quantity of about 300 angstroms. The
ordinate represents the photoelectric intensities of the elements emitted by the irradiation
with X-rays, i.e., represents the kinds and compositions of the metal exposed on the
surface of the metal substrate. In the initial stage of etching as shown in Fig. 1,
the electrons that are emitted are mostly those of chromium and chromium oxide, from
which it is recognized that the outermost surface of the steel plate has been completely
coated with chromium and chromium oxide. Then, as the etching proceeds, the emission
of electrons from chromium and chromium oxide decreases, and the emission of electrons
from tin and iron increase. That is, when the coating of the tin-containing metal
is complete and is continuous, no electron is emitted from iron. However, the fact
that the electrons are emitted from both tin and iron indicates that the iron-phase
and the tin-phase exist being mixed together in the steel plate which is coated with
the tin-containing metal but which is not coated with chromium yet. As the sputtering
proceeds, the photoelectric intensity of tin and the photoelectric intensity of iron
becomes nearly horizontal (steady state). In this case, it can be regarded that the
intensities are related to a ration of areas of the two metals on the reference surface
(before being plated) of the steel plate. In the measurement of the present invention,
the photoelectric intensity of iron at this moment is denoted by VFe. As the sputtering
is further carried out, tin is removed by etching and the photoelectric intensity
of tin becomes almost zero. At this moment, the surface of the steel plate consists
almost all of iron. If the photoelectric intensity of iron at this moment is denoted
by VFeo, then the ratio VFe/VFe represents the ration of exposed areas of the steel
plate. Therefore, a value obtained by subtracting the above ratio from 1 represents
a coating factor of tin.
[0016] In the steel plate coated with the tin-containing metal used in the present invention,
the steel plate assumes the sea-like distribution and the tin-containing metal layer
assumes the island like-distribution. In additions, the tin-containing metal layer
exists in a homogeneous and minute condition. Fig. 3 is a microphotograph of a tin
plate having a coating rate PSn of a tin containing metal of 47% at a magnification
of 400 times, wherein black portions are seas of the steel and white portions are
islands of the tin-containing metal layer. The steel portions help increase the adhesive
force of the organic resin coating layer via a metal chromium-chromium oxide layer,
and the tin-containing metal layer portions elute out to prevent the underlying steel
from corroding and to prevent the metal from eluting out. Therefore, even when the
above can material is subjected to the deep drawing or to the treatment for reducing
the thickness, the organic resin coating material does not at all peel off. Moreover,
even when the organic resin coating material is partly damaged by the treatment, the
damaged portions are not corroded by the acidic beverages or sports beverages.
[0017] Fig. 4 is a diagram of characteristic showing a change in the corrosion resistance
(discoloration evaluation) when the coating rate PSn of the tin-containing metal is
changed and a change in the adhesive force of the organic resin and chromium coating.
It will be understood from Fig. 4 that the corrosion resistance suddenly increases
as the coating rate PSn exceeds 20% and that the corrosion resistance decreases as
the coating rate PSn exceeds 80% to make it difficult to perform the deep drawing.
When the coating rate PSn is 100%, the adhesive force so decreases that the deep drawing
can no longer be carried out even though the tin and metal chromium coatings are perfect
(point P in Fig. 4).
Brief description of the Drawings
[0018]
Fig. 1 is a graph showing the measured results of a surface-treated can material used
in the present invention as measured by the X-ray photoelectric spectroscopic method;
Fig. 2 is a schematic diagram of the can material in cross section;
Fig. 3 is a microphotograph showing a particulate structure on the surface of the
steel plate coated with the tin-containing metal that is used in the present invention;
Fig. 4 is a diagram showing correlations among the coating rate of tin on the can
material, adhesive force of the organic coating material, and the corrosion resistance;
and
Fig. 5 is a diagram of steps for drawing the can material.
Description of a Preferred Embodiment
[0019] A preferred embodiment of a deeply drawn can according to the present invention will
now be described in conjunction with the accompanying drawings.
[0020] Fig. 2(A) is a schematic sectional view of the can material used in the present invention,
wherein a surface-treatment layer 4 of a tin-containing metal is formed on the surface
of a steel plate 2, and a surface-treatment layer 6 of metal chromium and a hydrated
chromium oxide is further formed thereon. The layer 6 of metal chromium and hydrated
chromium oxide is formed to completely cover the surface of the steel plate 2 and
the surface of the tin-containing metal layer 4, and an organic resin layer 8 is further
formed on the surface of the layer 6 of metal chromium and hydrated chromium oxide.
The layer of chromium and hydrated chromium oxide and the organic resin layer 8 are
drawn in Fig. 2(A) exaggerating the thickness. In the present invention, furthermore,
the surface treatment layer 4 of the tin-containing metal is applied onto the surface
of the steel plate 2 at a coating rate PSn over a range of from 20 to 80% as shown
in Fig. 3.
[0021] Fig. 2(B) schematically illustrates the state in which the photoelectric intensities
of tin and iron remain constant as measured by the X-ray photoelectric spectroscopic
method mentioned earlier and wherein islands 9 of the tin-containing metal are floating
on the sea of steel.
[0022] The steel plate substrate should generally be a rolled steel plate such as the one
that has heretofore been used for producing cans. The steel plate should have a thickness
of, usually, from 0.05 to 0.35 mm, and particularly from 0.07 to 0.30 mm though it
varies depending upon the size of the final cans.
[0023] It is desired that the tin-containing metal is applied to the steel plate in an amount
of 100 to 5000 mg/m⁻² and, particularly, in an amount of 100 to 4000 mg/m⁻². When
the coating amount becomes smaller than the above range, the tin-containing metal
layer 4 shown in Fig. 2(A) is not sufficiently formed, and the coating rate PSn may
often become smaller than 20%. When the coating amount exceeds the above range, on
the other hand, the coating rate PSn becomes too great and the adhesive force decreases.
[0024] The tin-containing metal may be an alloy with iron, nickel or any other metal, but
its content should at least be greater than 20%. When the content of tin is smaller
than the above-mentioned range, the corrosion resistance of the deeply drawn can is
not sufficiently enhanced.
[0025] In order to form the tin-containing metal layer maintaining the sea-island relationship
according to the present invention, the plated layer is precipitated in a granular
form, and the plated steel plate is not subjected to the reflow processing but is
washed with, for example, hydrochloric acid or a like acid of 1 to 7 N, so that the
coating rate PSn lies within a range specified by the present invention.
[0026] In general, the coating rate PSn decreases with an increase in the degree of washing
with acid. Therefore, the hydrochloric acid concentration, temperature of processing
and the processing time should be suitably set on this basis.
Coating layer of metal chromium and hydrated chromium oxide.
[0027] The coating layer of chromium and a hydrated chromium oxide should be so provided
as to sufficiently cover the surface of the steel plate and the surface of the tin-containing
coating layer. A preferred example of the surface treatment is the electrolytic treatment
with chromic acid to provide a metal chromium layer in an amount of 10 to 200 mg/m⁻²
and a chromium oxide layer in an amount of 1 to 50 mg/m⁻² (reckoned as metal chromium).
This layer is excellent in both organic film adhesion and corrosion resistance.
Organic resin coating layer.
[0028] Examples of the organic resin coating include a variety of thermoplastic resin films
and thermosetting or thermoplastic resin films. Furthermore, preferred examples of
the crystalline thermoplastic resin film include olefin-type resin films such as of
polyethylene, polypropylene, ethylene-propylene copolymer, ethylene-vinyl acetate
copolymer, ethylene-acrylic ester copolymer and ionomer; polyester films such as of
polyethylene terephtalate, polybutylene terephtalate, ethylene terephtalate/isophthalate
copolymer, ethylene terephthalate/adipate copolymer, ethylene terephthalate/sebacate
copolymer, and butylene terephthalate/isophthalate copolymer; polyamide films such
as nylon 6, nylon 6,6, nylon 11 and nylon 12; polyvinyl chloride films; and polyvinylidene
chloride films. These films may be unstretched or may be biaxially stretched. Their
thickness should generally be from 3 to 50 µm and, particularly, from 5 to 40 µm.
[0029] The film is laminated on the metal plate by the heat-melting method, the dry lamination
or the extrusion coating method. When the adhesiveness (melt-adhering property) is
poor, there can be interposed, for example, an urethane-type adhesive, an epoxy-type
adhesive, an adhesive of the type of an acid-modified olefin resin, a copolyamide-type
adhesive, a copolyester-type adhesive or an adhesive primer that is described below
between the film and the metal plate. As the adhesive primer, there can be used a
coating material that exhibits excellent adhesiveness to the metal plate, excellent
anti-corrosing property, and excellent adhesiveness to the resin film. As the adhesive
primer, there can be used an epoxy resin and a curing resin for the epoxy resin, such
as a coating material consisting of a combination of a phenol resin, an amino resin,
an acrylic resin and a vinyl resin, and particularly an epoxy-phenol coating material,
or an organosol-type coating material composed of a vinyl chloride copolymer resin
and an epoxy resin-type coating material. The adhesive primer or the adhesive agent
should have a thickness of from 0.1 to 5 µm.
[0030] To effect the lamination, the adhesive primer or the adhesive agent is applied to
either one or both of the metal and the film followed, as required, by drying or partial
curing. Then, the two are pressed and adhered together into a unitary form under the
application of heat. During the step of lamination, the biaxial molecular orientation
in the film may slightly be loosened which, however, does not at all affect the drawing
or the redrawing and may often turn out to be desirable from the standpoint of drawing
operation.
Other compositions.
[0031] An inorganic filler (pigment) can be contained in the film for outer surface for
the purpose of concealing the metal plate and assisting the transmission of wrinkle-suppressing
force to the metal plate at the time of drawing and redrawing. Examples of the inorganic
filler include inorganic white pigments such as rutile-type or anatase-type titanium
dioxide, zinc flower, gloss white and the like; white body pigments such as barite,
sedimenting barite sulfate, calcium carbonate, gypsum, sedimenting silica, aerosil,
talc, sintered or unsintered cray, barium carbonate, alumina white, synthetic or natural
mica, synthetic calcium silicate, and magnesium carbonate; black pigments such as
carbon black, magnetite, and the like; red pigments such as red iron oxide, yellow
pigments such as sienna, and the like; and blue pigments such as ultramarine, cobalt
blue, and the like. These inorganic fillers can be blended in an amount of 10 to 500%
by weight and, particularly, in an amount of 10 to 300% by weight with respect to
the resin.
[0032] A protective coating material that can be used instead of, or together with, the
film may be any protective coating material comprising thermosetting and thermoplastic
resins. Examples include modified epoxy coating materials such as phenol-epoxy coating
material, amino-epoxy coating material; vinyl or modified vinyl coating materials
such as vinyl chloride-vinyl acetate copolymer, partially saponified product of vinyl
chloride-vinyl acetate copolymer, vinyl chloride-vinyl acetate-maleic anhydride copolymer,
epoxy-modified, epoxyamino-modified, or epoxyphenol-modified vinyl coating material;
acrylic resin-type coating material; and synthetic rubber-type coating material such
as styrene-butadiene-type copolymer, and the like, which can be used alone or in a
combination of two or more kinds.
[0033] These coating materials are applied to the metal material in the form of an inorganic
solvent solution such as enamel, lacquer or the like, in the form of an aqueous dispersion
or aqueous solution, or by the roller coating, spray coating, immersion coating, electrostatic
coating, or electrophoretic coating. The above resin coating material is baked, as
required as a matter of course, when it has a thermosetting property. From the standpoint
of corrosion resistance and processability, it is desired that the protective coating
material has a thickness (dry state) which is usually from 2 to 30 µm and, particularly,
from 3 to 20 µm. In order to improve the drawing-redrawing property, furthermore,
a variety of lubricating agents may be contained in the coated film.
Drawing.
[0034] In the steps of drawing and redrawing as shown in Fig. 5, a coated metal plate 10
is punched into a disc, a predrawn cup 13 having a bottom portion 11 and a side wall
12 is formed in a predrawing step using a predrawing punch of a large diameter and
a die, the predrawn cup 13 is held by an annular holding member which is inserted
in the cup and a redrawing die (not shown), a deeply drawn cup 16 having a diameter
smaller than that of the predrawn cup is formed by moving a redrawing punch and the
redrawing die in mesh with each other and relative to each other, the redrawing punch
and the redrawing dies being provided in concentric with the holding member and the
redrawing die so as to go into and come out from the holding member, and a cup 19
having a smaller diameter is formed by similarly effecting the drawing.
[0035] Reference numerals 14 and 17 denote bottom portions of the cups 16 and 19, and reference
numerals 15 and 18 denote side walls of the cups 16 and 19. In carrying out the redrawing,
it is desired to bend and stretch the coated metal plate by the action corner of the
redrawing die in order to reduce the thickness, or to slightly squeeze the coated
metal plate between the redrawing punch and the redrawing die during the redrawing
steps in order to reduce the thickness.
[0036] In Fig. 5, the side walls of the cups usually have a relationship,

[0037] It is desired that the drawing ratio defined by an equation,

usually lies within a range of from 1.2 to 2.0 and, particularly, from 1.3 to 1.9.
It is further desired that the redrawing ratio defined by an equation,

usually lies within a range of from 1.1 to 1.6 and, particularly, from 1.15 to 1.5.
[0038] Furthermore, the degree of reduction of thickness of the side wall should usually
be about 5 to 45 % and, particularly, about 5 to 40% of the thickness of the material
plate (thickness of the bottom portion). It is desired that the drawing and redrawing
are carried out under the conditions where molecular orientation takes place in the
resin layer. For this purpose, the drawing and redrawing should be carried out at
a stretching temperature of the resin layer, such as at a temperature of 20° to 200°C
in the case of the PET.
[0039] In carrying out the drawing and redrawing, it is desired that the coated metal plate
or the cup is further coated with various lubricants such as liquid paraffin, synthetic
paraffin, edible oil, hydrogenated edible oil, palm oil, various natural waxes or
polyethylene wax. The lubricant should be applied in an amount of usually from 0.1
to 10 mg/dm⁻² and, particularly, in an amount of 0.2 to 5 mg/dm⁻² though it may vary
depending on the kind thereof. The lubricant is applied to the surface in a molten
state by spray coating. The deeply drawn can that is obtained is them subjected to
the after-treatment such as washing with water and drying, and is further subjected
to the doming, trimming, neck-in treatment, bead treatment and flange treatment, in
order to obtain a final barrel of can. Even in the above treatment steps, the organic
resin coating material excellently follows the steel plate.
Examples and comparative Examples
Example 1:
[0040] A cold-rolled steel plate having a thickness of 0.15 mm and a tempering degree of
DR-9 was washed with an acid and on which tin was plated using an ordinary stannous
phenol sulphonate bath at a current density of 0.5 A/m⁻² followed by washing with
hydrochloric acid in order to obtain a tin-plated steel plate having a tin amount
of 1.2 g/m⁻² and a tin coating rate of 50%.
[0041] The tin-plated steel plate was then subjected to the ordinary electrolytic treatment
with chromic acid to plate metal chromic in an amount of 120 mg/m⁻² and to plate a
hydrated chromium oxide in an amount of 15 mg/m⁻² in a laminated form. The tin coating
rate was calculated from the formula (1) by effecting the analysis based on the XPS
(X-ray photoelectric spectroscopic) method.
[0042] A biaxially stretched polyethylene terephthalate film (melting point, 230°C) having
a thickness of 20 µm to which has been applied an epoxyphenol-type adhesive primer
was thermally adhered to a surface of the thus obtained steel plate that would become
the inner surface of the can and, at the same time, a titanium dioxide-containing
biaxially stretched polyethylene terephthalate/isophthalate film (melting point, 230°C)
having a thickness of 15 µm to which has been applied a similar adhesive primer was
thermally adhered to the surface of the steel plate that would become the outer surface
of the can, in order to obtain a metal plate coated with resin. The palm oil was applied
to the thus coated metal plate which was then punched into a disk having a diameter
of 187 mm to form a shallowly drawn cup in accordance with the customary method. In
the above drawing step, the drawing ratio was 1.4.
[0043] In the subsequent first, second and third redrawing steps, the cup was preheated
at 80°C, and the redrawing was carried out. In the first to third redrawing steps,
the redrawing conditions were as follows:

[0044] In order to reduce the thickness of the drum of can, the redrawing was effected by
bending. The drawing and redrawing thus effected developed no problem in the processability,
and the deeply drawn cup exhibited the following properties.
- Diameter of the cup
- 66 mm
- Height of the cup
- 140 mm
- Rate of change in the thickness of side wall
- -20%
[0045] Thereafter, the doming was effected according to a customary method, the palm oil
was removed by washing with water and, then, the trimming was effected. Next, in the
step of printing, printing was effected to the outer surface using an ordinary ink
and a finishing varnish, followed by baking and neck-in/flange treatment, in order
to obtain a deeply drawn coated can having a reduced thickness.
[0046] In this case, the rate of metal tin in the tin layer was 70% as measured by an electrochemical
method (supplement to JIS-G3303) by using the bottom portion of the deeply drawn coated
can as a sample and after the organic resin coating material was removed by being
immersed in an aqueous solution of peroxide at 90°C.
[0047] The thus obtained deeply drawn coated can could be treated without permitting the
coating material to be peeled off during the step of treatment. Thereafter, an orange
juice was contained therein being heated at 95°C while permitting liquid nitrogen
to drop thereon, and the cover was seamed. The orange juice was preserved fro extended
periods of time at 37°C to observe the corroding condition on the inner surface of
the can pit corrosion and the leakage through the pore. No abnormal condition, however,
was recognized . The results were as shown in Table 1.
Example 2:
[0048] A deeply drawn can was obtained by effecting the coating and treatment in the same
manner as in Example 1 but plating tin in an amount of 3.2 g/m⁻² and changing the
tin coating rate into 76%. The results were as shown in Table 1.
Example 3:
[0049] A deeply drawn can was obtained by effecting the coating and treatment in the same
manner as in Example 1 but plating tin in an amount of 520 mg/m⁻² and changing the
tin coating rate into 26%. The results were as shown in Table 1.
Example 4:
[0050] A deeply drawn can was obtained by effecting the coating and treatment in the same
manner as in Example 1 except that an alloy layer was formed on the interface between
the tin layer and the steel and the ratio of metal tin in the tin layer was 45% since
the biaxially stretched polyethylene terephthalate/isophthalate film was heat-adhered
onto the plated steel plate at a temperature that was as high as nearly the melting
point of the film. The results were as shown in Table 1.
Example 5:
[0052] A deeply drawn can was obtained by effecting the coating and treatment in the same
manner as in Example 1 except that an epoxyphenol resin coating material was so applied
and baked on the surface of the plated steel plate that would become the inner surface
of the can that the thickness of the coated film after drying was 15 µm and the epoxyphenol
resin coating material was so applied and baked on the surface that would become the
outer surface of the can that the thickness of the coated film after drying was 15
µm, the ratio of metal tin in the tin layer being 55%. The results were as shown in
Table 1.
Comparative Example 1:
[0053] The coating and treatment were carried out in the same manner as in Example 1 except
that the cold-rolled steel plate having a thickness of 0.15 mm and a tempering degree
of DR-9 was washed with an acid an on which tin was plated using an ordinary stannous
phenol sulphonate bath at a current density of 1.5 A/m⁻² to obtain a tin-plated steel
plate having a tin amount of 3.7 g/m⁻² and a tin coating rate of 100%, and then the
tin-plated steel plate was subjected to the ordinary electrolytic treatment with chromic
acid to plate metal chromium in an amount of 120 mg/m⁻² and to plate a hydrated chromium
oxide in an amount of 15 mg/m⁻² in a laminated form. After the redrawing of the third
time, however, the resin coating layer was partly peeled off on the drum portion of
the cup, and the subsequent treatment could not be carried out.
Comparative Example 2:
[0054] A deeply drawn can was obtained by effecting the coating and treatment in the same
manner as in Example 1 with the exception of using a so-called steel plate without
tin that was obtained by washing the cold-rolled steel plate having a thickness of
0.15 mm and a tempering degree of DR-9 with an acid and subjecting the steel plate
to an ordinary electrolytic treatment with chromic acid to plate metal chromium in
an amount of 120 mg/m⁻² and a hydrated chromium oxide in an amount of 15 mg/m⁻² in
a laminated form. The results were as shown in Table 1.
Comparative Example 3:
[0055] A deeeply drawn can was obtained by effecting the coating and treatment in the same
manner as in Example 1 except that tin was plated in an amount of 400 mg/m⁻² and tin
coating rate was 15%. The results were as shown in Table 1.
Comparative Example 4:
[0056] A deeply drawn coated can was obtained by effecting the coating and treatment in
the same manner as in Example 1 except that in was plated in an amount of 3.8 g/m⁻²
and a tin coating rate was 85%. At the time of deep drawing, neck-in treatment and
seaming, however, it was observed that the resin coating had been partly peeled off.
The results obtained were as shown in Table 1.

[0057] According to the present invention, a tin-containing metal is applied onto the surface
of the steel plate at a coating rate of 20 to 80%, and then metal chromium and a hydrated
chromium oxide are applied thereon, in order to form an organic resin coating layer
on the steel plate which is then deeply drawn to obtain a can. Therefore, the organic
resin coating layer of the deeply drawn can remains sufficiently adhered to the surface
of the steel plate despite the presence of the tin-containing metal layer, and is
not peeled off at all even after the aforementioned deep drawing, doming, trimming,
neck-in treatment, beading and flange treatment. Moreover, since the tin-containing
metal exists in an amount larger than a required amount, there takes place sacrificial
dissolution of tin lending the cans well suited for storing even acidic beverages
that have highly corrosive properties.
1. A deeply drawn can having excellent corrosion resistance made of a laminated material
which comprises:
a metal substrate having a steel plate, a tin-containing metal applied thereon
at a coating rate defined by the formula,

wherein VFe represents a photoelectric intensity of iron at a moment when the
photoelectric intensity of iron (Fe) and the photoelectric intensity of tin (Sn) have
entered into nearly a steady state while subjecting the surface of the steel plate
to be coated to an X-ray photoelectric spectroscopy, at the etching treatment of the
surface of said steel plate, and VFeo represents a photoelectric intensity of iron
at a moment when the etching is further carried out and the photoelectric intensity
of tin (Sn) becomes substantially zero,
of 20 to 80%, metal chromium and a hydrated chromium oxide which are applied onto
the whole surface of the steel plate coated with the tin-containing metal; and
an organic resin coating applied onto the surface of said metal substrate.
2. A deeply drawn can according to claim 1, wherein the tin-containing metal layer consists
of a tin layer, a tin-iron alloy layer, or a tin-nickel alloy layer.
3. A deeply drawn can according to claim 1, wherein the organic resin coating layer consists
of a film layer of a biaxially stretched polyester or copolyester that is thermally
adhered via an epoxy-phenol resin-type primer.
4. A deeply drawn can according to claim 1, wherein the metal chromium layer is provide
in a coating amount of 10 to 200 mg/m² and the hydrated chromium oxide layer is provided
in a coating amount of 1 to 50 mg/m² reckoned as a metal.
5. A deeply drawn can according to claim 1, wherein the tin-containing metal layer is
homogeneously and uniformly distributed on the steel plate substrate as a plated layer
having a sea-island relationship of an average size in the plane direction of 0.1
to 10 µm.
6. A redrawing method wherein a shallowly predrawn cup is formed by drawing a laminated
material which comprises:
a metal substrate having a steel plate, a tin-containing metal applied thereon
at a coating rate defined by the formula,

wherein VFe represents a photoelectric intensity of iron at a moment when the
photoelectric intensity of iron (Fe) and the photoelectric intensity of tin (Sn) have
entered into nearly a steady state while subjecting the surface of the steel plate
to be coated to an X-ray photoelectric spectroscopy, at the etching treatment of the
surface of said steel plate, and VFeo represents a photoelectric intensity of iron
at a moment when the etching is further carried out and the photoelectric intensity
of tin (Sn) becomes substantially zero,
of 20 to 80%, metal chromium and a hydrated chromium oxide which are applied onto
the whole surface of the steel plate coated with the tin-containing metal; and
an organic resin coating applied onto the surface of said metal substrate;
and wherein said predrawn cup is held by an annular holding member inserted in
said cup and by a redrawing die, a deeply drawn cup having a diameter smaller that
of said predrawn cup is formed by moving a redrawing punch and the redrawing die relative
to each other in mesh with each other, said redrawing punch and said redrawing die
being provided in concentric with the holding member and the redrawing die so as to
go into and come out from the holding member, and the whole side wall of the cup is
uniformly bent in the direction of the height to reduce the thickness of the side
wall of the cup.
7. A method according to claim 6, wherein the radius of curvature (RD) of the action
corner of the redrawing dies is 1 to 2.9 times as great as the thickness (tB) of the
metal plate, the radius of curvature (RD) of the holding corner of the holding member
is 4.1 to 12 times as great as the thickness (tB) of said metal plate, the plane engaging
portions of the holding member and the redrawing die that engage with the predrawn
cup have a dynamic coefficient friction of 0.001 to 0.2, and at least one stage of
drawing is effected so that a redrawing ratio defined as a ratio of the diameter of
the shallowly drawn cup to the diameter of the deeply drawn cup lies within a range
of 1.1 to 1.5.