FIELD OF THE INVENTION
[0001] The present invention relates to a green sand mold suitable for producing a cast
stainless steel article known as a particularly hard-to-cut material, and its production
method, and a method for producing a cast steel article using such a green sand mold.
BACKGROUND OF THE INVENTION
[0002] Casting sand constituting green sand molds for producing cast steel articles generally
comprises aggregates (sand), a binder such as bentonite, etc., carbonaceous components
(coal, starch, etc.) as secondary additives, and water. The ratios of aggregates,
a binder, etc. in the casting sand are properly determined to provide the green sand
molds with desired properties [air permeability, strength, the stability of cavity
surfaces, and compactability (CB), etc.]. Carbonaceous components such as coal powder,
coke powder, graphite powder, pitch powder, etc. added to the casting sand prevent
the sticking of aggregates (sand) to castings (sand seizure), thereby stabilizing
the as-cast surface quality of cast steel articles. Technologies concerning coal are
disclosed in
JP 63-177939 A and
JP 2009-291801 A.
[0003] JP 63-177939 A discloses a method for producing a casting green sand mold by blending 1-2 parts
of an additive for a casting sand mold, which comprises 10-90% by weight of a mineral
oil and 90-10% by weight of a carbonaceous material; 100 parts of aggregate, 10 parts
of bentonite (binder), 1 part of starch, and 3 parts of water; and forming the resultant
casting sand into the green sand mold.
JP 2009-291801 A discloses casting sand for a green sand mold, which comprises a carbonaceous additive
comprising as a main component an edible vegetable oil containing glycerin, bentonite
(binder), and if necessary, additives such as starch, etc., and a predetermined amount
of water.
[0004] However, when cast steel articles having hypo-eutectoid compositions containing about
0.05-0.60% by mass of carbon are produced by green sand molds formed by casting sand
containing the additives disclosed in
JP 63-177939 A and
JP 2009-291801 A, which include mineral oils, carbonaceous materials or vegetable oils, the cast steel
articles may have as-cast surfaces carburized by carbonaceous components contained
in the green sand molds. With the carburized as-cast surface layers, cast steel articles
are not easily machined. This problem is particularly serious in cast stainless steel
articles needing high heat resistance and corrosion resistance, which are used, for
example, as exhaust members for internal combustion engines.
OBJECT OF THE INVENTION
[0005] Accordingly, an object of the present invention is to provide a green sand mold for
producing a cast steel article with suppressed sand seizure and carburization on an
as-cast surface layer while keeping as good as-cast surface quality as conventional
one, and its production method, and a method for producing a cast steel article using
such a green sand mold.
DISCLOSURE OF THE INVENTION
[0006] As a result of intensive research to satisfy two contradicting objects of suppressing
the carburization of an as-cast surface layer while keeping as good as-cast surface
quality (sand seizure) as conventional one, it has been found that (1) by reducing
the ratio of a carbonaceous component in casting sand constituting a green sand mold
to such a level as not generating carburization, and (2) by setting the thickness
of a coating layer of a thermosetting resin formed on a recess of a green sand mold,
to such a level that (a) a cavity surface is covered with a gas generated by the decomposition
of the thermosetting resin until a melt introduced into the cavity starts to be solidified,
thereby preventing sand seizure, and that (b) the decomposition gas disappears immediately
after the solidification of the melt, the as-cast surface quality can be kept while
suppressing the carburization of an as-cast surface layer. The present invention has
been completed based on such finding.
[0007] Thus, the green sand mold of the present invention for producing a cast steel article
is formed by casting sand comprising sand, a binder, and 3 parts or less by mass of
a carbonaceous component per 100 parts by mass of the sand;
at least a recess including a cavity for forming the cast steel article being provided
with a coating layer of a thermosetting resin; and
the coating layer having average hardness (measured by a self-hardening hardness meter)
of 50-95 and a thickness of 0.5-2.5 mm.
[0008] The amount of the thermosetting resin forming the coating layer is preferably 100-500
g/m
2 on a solid basis.
[0009] The amount of carbon remaining in a unit volume of the coating layer is preferably
20-200 mg/cm
3 after heated to 800°C at a speed of 10°C/minute in the air.
[0010] The method of the present invention for producing the above green sand mold comprises
forming casting sand comprising sand, a binder, and 3 parts or less by mass of a carbonaceous
component per 100 parts by mass of sand, into at least a pair of green sand mold parts
(for example, upper and lower mold parts), which comprises a recess including a cavity
for forming the cast steel article;
coating at least the recess with a coating solution comprising a thermosetting resin
and an organic solvent; and
thermally curing the thermosetting resin coated on the recess, to form a coating layer
having average hardness (measured by a self-hardening hardness meter) of 50-95.
[0011] The thermosetting resin may be thermally cured before and/or after combining the
green sand mold parts. In the first embodiment, at least a pair of green sand mold
parts are combined after thermally curing the thermosetting resin. In the second embodiment,
the hardening of a coating layer obtained by drying the coating solution is carried
out by a first hardening step of heating to average hardness (measured by a self-hardening
hardness meter) of 30-45, and a second hardening step of further heating the primarily
hardened coating layer to average hardness (measured by a self-hardening mold hardness
tester) of 50-95.
[0012] The coating solution preferably has a viscosity of 15-100 mPa·s.
[0013] The method of the present invention for producing a cast steel article uses the above
green sand mold.
EFFECTS OF THE INVENTION
[0014] Because the green sand mold of the present invention formed by casting sand containing
3 parts or less by mass of a carbonaceous component per 100 parts by mass of sand
comprises a recess, on which a coating layer of a thermosetting resin having average
hardness (measured by a self-hardening hardness meter) of 50-95 and a thickness of
0.5-2.5 mm is formed, a cast steel article having less carburized as-cast surface
layer can be produced while keeping as good as-cast surface quality as conventional
one.
BRIEF DESCRIPTION OF THE DRAWINGS
[0015]
Fig. 1 is a cross-sectional view showing the structure of the green sand mold of the
present invention.
Fig. 2 is an enlarged partial cross-sectional view showing a portion A in Fig. 1.
Fig. 3(a) is a cross-sectional view showing a mold-forming step in the first example
of the production processes of the green sand mold shown in Fig. 1.
Fig. 3(b) is a cross-sectional view showing a
coating-solution-applying step in the first example of the production processes of
the green sand mold shown in Fig. 1.
Fig. 3(c) is a cross-sectional view showing a
thermosetting-resin-curing step in the first example of the production processes of
the green sand mold shown in Fig. 1.
Fig. 3(d) is a cross-sectional view showing a molds-combining step in the first example
of the production processes of the green sand mold shown in Fig. 1.
Fig. 4(a) is a cross-sectional view showing a mold-forming step in the second example
of the production processes of the green sand mold shown in Fig. 1.
Fig. 4(b) is a cross-sectional view showing a
coating-solution-applying step in the second example of the production processes of
the green sand mold shown in Fig. 1.
Fig. 4(c) is a cross-sectional view showing a first thermosetting-resin-curing step
in the second example of the production processes of the green sand mold shown in
Fig. 1.
Fig. 4(d) is a cross-sectional view showing a molds-combining step in the second example
of the production processes of the green sand mold shown in Fig. 1.
Fig. 4(e) is a cross-sectional view showing a second thermosetting-resin-curing step
in the second example of the production processes of the green sand mold shown in
Fig. 1.
Fig. 5(a) is an enlarged schematic view showing casting sand (before coated with a
thermosetting resin) constituting the green sand mold.
Fig. 5(b) is an enlarged schematic view showing
thermosetting-resin-coated casting sand constituting the green sand mold.
Fig. 6 is a cross-sectional view showing the production method of a cast steel article
using the green sand mold shown in Fig. 1.
Fig. 7 is an enlarged partial cross-sectional view showing a portion B in Fig. 6.
Fig. 8(a) is a SEM photograph (100 times) showing casting sand constituting the green
sand mold of Example 1.
Fig. 8(b) is a SEM photograph (100 times) showing phenol-resin-coated casting sand
constituting the green sand mold of Example 1.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0016] The embodiments of the present invention will be explained in detail below referring
to the attached drawings, without intention of restricting the present invention thereto.
Explanations of each embodiment will be applicable to other embodiments unless otherwise
mentioned.
[0017] Fig. 1 shows the structure of the green sand mold of the present invention, Fig.
2 enlargedly shows a portion A in Fig. 1, Figs. 3 and 4 show the production steps
of the green sand mold shown in Fig. 1, and Fig. 6 shows a production step of a cast
steel article using the green sand mold of Fig. 1. The term "cast steel article" used
herein means a casting having a hypo-eutectoid composition comprising 0.05-0.6% by
mass of C and other elements (Ni, Cr, Si, W, Mo, Nb, etc.), the balance being Fe and
inevitable impurities, though not restrictive.
[1] Structure of green sand mold
[0018] As shown in Fig. 1, a green sand mold 1 formed by casting sand containing substantially
no carbonaceous component is constituted by an upper mold part 1a and a lower mold
part 1b combined along a parting surface 1e. The green sand mold 1 obtained by combining
the upper mold part 1a and the lower mold part 1b comprises a cavity (article-forming
cavity) 1c for forming an article, and a runner 1d. The article-forming cavity 1c
and the runner 1d are formed by recesses in the upper mold part 1a and the lower mold
part 1b. Of course, the green sand mold 1 may be encircled by a flask. In addition
to the article-forming cavity 1c and the runner 1d, the green sand mold 1 may comprise
a riser, a gate, a sprue, etc.
(A) Casting sand
[0019] The casting sand comprises sand, a binder, and a carbonaceous component.
(1) Sand
[0020] As aggregate constituting the casting sand, sand per se may be usual one, which may
be, for example, mountain sand, semi-synthesized sand or synthesized sand. The mountain
sand may be natural sand containing at least 2% of clay, for example, Noma sand in
Aichi Prefecture, Kawachi sand in Osaka, Shima sand in Mie Prefecture, Matsue sand
in Shimane Prefecture, Ohta sand in Fukushima Prefecture, etc. as well as Enshu sand,
Genkai sand, etc. The semi-synthesized sand may be mountain sand properly blended
with silica sand, a binder and additives. The synthesized sand may be silica sand,
etc. blended with a binder and additives without using mountain sand at all. Sand
for the synthesized sand may be natural silica sand such as Gairome silica sand, beach
sand and river sand, artificial silica sand, zirconium silicate, olivine sand, chromite
sand, etc.
(2) Binder
[0021] The binder may be bentonite, clay, montmorillonite, kaolin, etc. The amount of the
binder is generally 5-12 parts by mass per 100 parts by mass of sand, though properly
adjustable depending on the characteristics of the green sand mold.
(3) Carbonaceous component
[0022] The carbonaceous component may be a carbonaceous material such as coal, graphite,
cokes, pitch cokes, asphalt, etc.; a starch-type additive such as dextrin, starch,
etc.; a liquid oil such as mineral oil, vegetable oil, etc. The carbonaceous component
does not include a carbon compound contained in sand or a binder. The carbonaceous
components may be used alone or combined.
[0023] To prevent the carburization of a cast steel article, the carbonaceous component
is 3 parts or less by mass per 100 parts by mass of sand in the present invention.
When casting is conducted using a green sand mold in which the carbonaceous component
is more than 3 parts by mass of the casting sand, a cast surface layer is carburized.
The amount of the carbonaceous component is more preferably 1 part by mass, most preferably
0.7 parts or less by mass.
(B) Coating layer
[0024] As shown in Figs. 1 and 2, at least a surface layer of the article-forming cavity
1c is provided with a coating layer 1f made of a thermosetting resin having average
hardness of 50-95 (measured by a self-hardening hardness meter). To achieve the object
of the present invention of suppressing the carburization of a cast surface layer
while keeping a conventional level of as-cast surface quality, the coating layer 1f
need only be formed on the article-forming cavity 1c, though carburization can be
suppressed more effectively when a coating layer 1f is also formed on a runner 1d
through which a melt passes. Accordingly, the coating layer 1f is formed on at least
a recess including the cavity 1c and the runner 1d in the present invention. Further,
when a coating layer 1f is also formed on parting surfaces 1e, the parting surfaces
1e can have increased strength, suppressing the breakage of the mold, etc. when the
melt is supplied.
[0025] The thermosetting resin is not particularly restricted, as long as it is a high-strength,
high-hardness thermosetting resin, which is not broken when combining the mold parts,
and easily gasified by decomposition by contact with a steel melt. It includes, for
example, phenol resins, epoxy resins, melamine resins, urea resins, unsaturated polyester
resins, alkyd resins, polyurethanes, thermally curable polyimides, etc. The thermoset
resin coating layer 1f has average hardness in a range of 50-95. The hardness of the
coating layer 1f is measured by a self-hardening mold hardness tester (NK-009 available
from Nakayama Co., Ltd.). The coating layer 1f cannot suppress sand seizure when having
too low average hardness. On the other hand, it cannot hold enough air permeability,
likely suffering gas defects, when having too high average hardness.
[0026] The thermosetting resin forming the coating layer 1f is gasified and partially carbonized
by contact with a high-temperature melt, leaving a carbonaceous component in a surface
layer of the article-forming cavity 1c. To prevent the carburization of an as-cast
surface layer effectively, the amount of residual carbon per a unit volume of the
coating layer 1f is preferably 200 mg/cm
3 or less, when heated from room temperature to 800°C at a speed of 10°C/minute in
the air. When the amount of residual carbon is too small, sand seizure likely occurs
because too little gas is generated. Accordingly, the amount of residual carbon is
preferably 20 mg/cm
3 or more. When the amount of residual carbon is too much, the carburization of an
as-cast surface layer cannot be prevented sufficiently. Accordingly, the upper limit
of the amount of residual carbon is preferably 200 mg/cm
3. The amount of residual carbon is more preferably 20-100 mg/cm
3. The amount of residual carbon is determined by the thermogravimetric analysis (TGA)
of a thermosetting resin.
[0027] As shown in Fig. 2, the green sand mold 1 formed by sand particles 1j and a binder
(not shown), etc. has a lot of voids (pores) 1i between sand particles 1j for enough
gas permeability. Because the coating solution containing a thermosetting resin in
an organic solvent intrudes into pores 1i in the surface layer of the article-forming
cavity 1c, the thermosetting resin remains on sand particles 1j in the surface layer,
after the coating solution is dried. As a result, a region comprising sand particles
1j covered with the thermosetting resin is formed in the surface layer of the article-forming
cavity 1c. This region is called "coating layer 1f." In the coating layer If, sand
particles 1j are covered with the thermosetting resin, leaving voids (pores) 1i. The
thickness T of the coating layer 1f is expressed by an average value, because the
thermosetting resin does not have uniform depth as shown in Fig. 2. The thickness
T of the coating layer 1f is measured at plural points (for example, 3 points) in
a cross section of the article-forming cavity 1c provided with the coating layer 1f,
and averaged.
[0028] When the coating layer 1f has too large thickness T, the undecomposed thermosetting
resin is carbonized, leaving a carbonaceous component by which the as-cast surface
layer is likely carburized. To prevent the carburization of an as-cast surface layer
effectively, the thickness T of the coating layer 1f is preferably 2.5 mm or less,
more preferably 2.0 mm or less, most preferably 1.5 mm or less. When the coating layer
1f has too small thickness T, the coating layer 1f easily peels during a casting operation,
so that a melt intruding into portions exposed by peeling of the coating layer 1f
comes into direct contact with sand in the green sand mold, resulting in sand seizure.
Accordingly, the thickness T of the coating layer 1f is preferably 0.5 mm or more.
[0029] What are important in the coating layer 1f are not only its thickness T but also
the amount of the coated thermosetting resin. The amount of the coated thermosetting
resin is expressed by the dry weight (g/m
2) of a thermosetting resin per a unit area. The amount of the coated thermosetting
resin is preferably 100-500 g/m
2. When the amount of the coated thermosetting resin is less than 100 g/m
2, sand seizure cannot be prevented. On the other hand, when the amount of the coated
thermosetting resin is more than 500 g/m
2, the green sand mold has too low air permeability. As a result, gas defects likely
occur, and the undecomposed thermosetting resin is carbonized, leaving a carbonaceous
component by which the as-cast surface layer is likely carburized. To prevent the
carburization of an as-cast surface layer effectively while keeping good as-cast surface
quality, the amount of the curable resin in the coating layer 1f is more preferably
220-380 g/m
2. The amount of the coated thermosetting resin can be determined by dividing the weight
increment ΔD (g) of the green sand mold after drying the coating solution by the coating
area (m
2) of the thermosetting resin.
[0030] The coating layer 1f preferably has air permeability of 70-150. When the coating
layer 1f has too low air permeability, the generated gas is trapped by a melt, likely
resulting in a cast steel article having defects such as pinholes, etc. When the coating
layer 1f has too high air permeability, the coating layer 1f peels, resulting in a
cast steel article having poor appearance and sand detachability. The air permeability
can be measured by a rapid method described in Attachment 3 of JIS Z 2601.
[2] Production method of green sand mold
(A) First example
(1) Mold-forming step
[0031] As shown in Fig. 3(a), casting sand obtained by blending predetermined amounts of
sand, a binder, a carbonaceous component and water is formed into an upper mold part
1a and a lower mold part 1b having recesses 1g-1, 1g-2 for an article-forming cavity
1c and a runner 1d. To provide a green sand mold with enough strength with easy forming,
the amounts of a binder and water added to the casting sand are generally 5-12 parts
by mass of a binder and 1-5 parts by mass of water per 100 parts by mass of sand,
though properly adjustable depending on the characteristics of a green sand mold.
[0032] The upper mold part 1a and the lower mold part 1b are formed, for example, by charging
the casting sand into each flask in which a casting model for an article-forming cavity,
a runner, etc. is placed, compressing the casting sand by a jolt squeeze method, etc.,
and finally removing the casting model.
(2) Coating step
[0033] In the upper mold part 1a and the lower mold part 1b, as shown in Fig. 3(b), surfaces
of the recesses 1g-1, 1g-2 for a cavity 1c and a runner 1d, and parting surfaces 1e
are coated with a coating solution 1k comprising a thermosetting resin and an organic
solvent to form coating layers 1f. Though not only the recesses 1g-1, 1g-2 but also
the parting surfaces 1e are coated with a coating solution 1k in the depicted example,
coating need only be conducted at least on the recesses 1g-1, 1g-2. To stabilize the
amount of coating to provide the coating layer 1f with uniform thickness, the coating
solution 1k is preferably sprayed by a horizontally moving nozzle 10 as shown in Fig.
3(b).
[0034] In order that a proper amount of a coating solution 1k intrudes into voids 1i between
sand particles 1j from the surfaces of the recesses 1g-1, 1g-2, the coating solution
1k preferably has viscosity (measured by a Brookfield viscometer according to JIS
K6910) of 15-100 mPa·s. As a result, a coating layer 1f having a thickness T of 0.5-2.5
mm is formed in surface layers of the recesses 1g-1, 1g-2. With too large viscosity,
the coating solution 1k does not easily intrude into the surface layers of the recesses
1g-1, 1g-2, resulting in a coating layer 1f formed only near the surfaces of the recesses
1g-1, 1g-2. Accordingly, the coating layer 1f easily peels, resulting in a cast steel
article having poor appearance and sand detachability. With too small viscosity, the
coating solution 1k intrudes excessively, resulting in too thick a coating layer 1f.
Though variable depending on the concentration of a thermosetting resin, the amount
of a coating solution 1k applied is preferably set such that the amount of a thermosetting
resin coated on the recesses 1g-1, 1g-2 is 100-500 g/m
2 on a solid basis as described above.
(3) Coating-layer-forming step
[0035] As shown in Fig. 3(c), the coating solution applied to the recesses 1g-1, 1g-2 of
the upper mold part 1a and the lower mold part 1b is heated to cure the thermosetting
resin. Heating may be conducted during or after evaporating the organic solvent. Thus
formed is a coating layer 1f having average hardness (measured by a self-hardening
hardness meter) in a range of 50-95. Though not particularly restrictive, the coating
solution 1k can be heated, for example, by hot air supplied from a horizontally moving
blower 11 as shown in Fig. 3(c), or by heaters arranged on a horizontal plane.
(4) Molds-combining step
[0036] As shown in Fig. 3(d), the upper mold part 1a and the lower mold part 1b each having
a coating layer 1f on each recess 1g-1, 1g-2 are combined, to form an integral green
sand mold 1 shown in Fig. 1.
(B) Second example
[0037] The second example of the production methods of a green sand mold 1 is explained
referring to Fig. 4. In Fig. 4, the same reference numerals are assigned to the same
portions as in Fig. 3, with their detailed explanations omitted. The second example
of the production methods of a green sand mold 1 is the same as the first example,
except for having the first and second hardening steps shown in Figs. 4(c) and 4(e).
[0038] In the second example, the recesses 1g-1, 1g-2 of the upper mold part 1a and the
lower mold part 1b formed in the mold-forming step shown in Fig. 4(a) are coated with
a coating solution 1k in the coating step shown in Fig. 4(b), and hot air is supplied
from a blower 11 to heat the coating solution 1k, thereby forming a semi-hardened
layer 1L, in the first hardening step shown in Fig. 4(c). After the upper mold part
1a and the lower mold part 1b each provided with a semi-hardened layer 1L are combined
in the molds-combining step shown in Fig. 4(d), hot air supplied from a blower 12
is introduced into a cavity 1c through a runner 1d, to thermally harden the semi-hardened
layer 1L to form a coating layer 1f, in the second hardening step shown in Fig. 4(e).
[0039] Before the second hardening step for forming a coating layer If, the semi-hardened
layer 1L is formed by pre-hardening in the first hardening step, to prevent the cracking,
etc. of the coating layer 1f by rapid hardening, thereby avoiding the cast steel article
from having poor appearance. From this aspect, the average hardness of the semi-hardened
layer 1L measured by a self-hardening hardness meter is preferably 30-45. In the second
example, too, the average hardness (measured by a self-hardening hardness meter) of
the coating layer 1f is preferably in a range of 50-95.
[0040] By the method of the present invention, a thin thermosetting resin layer is formed
on binder-bonded sand particles 1j [Fig. 5(a)]. As a result, a coating layer 1f having
voids 1i [Fig. 5(b)] is formed at least on the recesses 1g-1, 1g-2 of the green sand
mold 1.
[3] Production method of cast steel article
[0041] As shown in Fig. 6, a melt is introduced into the article-forming cavity 1c of the
green sand mold 1 constituted by the upper mold part 1a and the lower mold part 1b
each having a coating layer 1f through the runner 1d, thereby producing a cast steel
article with reduced carburization in an as-cast surface layer, while keeping as good
surface quality as conventional one with respect to sand seizure. The reasons therefor
are not necessarily clear, but may be presumed as follows: (a) When the coating layer
1f of the article-forming cavity 1c comes into contact with a high-temperature melt
M as shown in Fig. 7, the thermosetting resin in the coating layer 1f is substantially
completely gasified, thereby suppressing sand seizure by a gas (shown by arrows) generated
by the decomposition of the thermosetting resin; and (b) because as relatively thin
a coating layer 1f as 0.5-2.5 mm disappears immediately after coming into contact
with the melt M, and because the amount of a carbonaceous component in the casting
sand constituting the green sand mold 1 is as small as 3 parts or less by mass, the
solidifying melt M is in contact with carbon only in a short period of time, resulting
in the suppressed carburization of the as-cast surface layer. Cast steel articles
suffering less carburization have excellent machinability. A thermosetting resin,
which is gasified slightly later in a deep region of the coating layer 1f than in
a shallow region, contributes to prevent direct contact of the melt M with the casting
sand of the article-forming cavity 1c until the melt M is solidified.
[0042] The present invention will be explained in more detail with Examples below, without
intention of restricting the present invention thereto.
Example 1
(1) Sand-preparing step
[0043] 100 parts by mass of silica sand was mixed with 8.1 parts by mass of bentonite, 3.0
parts by mass of water, and 3 parts by mass of carbon powder, to prepare casting sand.
(2) Mold-forming step
[0044] Casting sand was charged into flasks in each of which a casting design model was
set, and compressed by a jolt-squeeze method to form upper and lower mold parts. Measurement
at five points by a self-hardening mold hardness tester (NK-009 available from Nakayama
Co., Ltd.) revealed that the average hardness of each recess of the upper and lower
mold parts was 20. Fig. 8(a) is a SEM photograph (100 times) showing a recess surface
of the formed green sand mold. As is clear from Fig. 8(a), there were a lot of voids
between binder-covered sand particles.
(3) Coating step
[0045] As shown in Table 2, a coating solution (viscosity: 20 mPa·s) comprising 40% by mass
of a phenol resin and 60% by mass of ethanol was applied to the recesses and parting
surfaces of the upper and lower mold parts. The amount of the coating solution applied
was 300 g/m
2 on a solid basis.
(4) Coating layer-forming step
[0046] The coating solution applied to the recesses and parting surfaces of the upper and
lower mold parts was thermally cured by an incandescent lamp, to form a coating layer.
Fig. 8(b) is a SEM photograph (100 times) showing a recess surface of the green sand
mold provided with the coating layer. As is clear from Fig. 8(b), there are sufficient
voids remaining between sand particles covered with the coating layer, making it possible
to sufficiently discharge a gas generated by the decomposition of the thermosetting
resin.
(a) Measurement of thickness T
[0047] Five blocks of 3 cm x 3 cm x 3 cm were cut out of recess surfaces of the upper and
lower mold parts provided with the coating layer by a spoon, and the casting sand
was removed from each block by a brush without destroying the coating layer. The thickness
of each sample consisting only of a hardened coating layer was measured by a venier
caliper. The thickness T of the hardened coating layer, which was determined by averaging
the measured thickness values of all blocks, was 1.1 mm.
(b) Measurement of amount of residual carbon
[0048] After thickness measurement of the coating layer, each sample, whose coating layer
had a volume of 3 x 3 x T cm
3, with a surface area of 3 x 3 cm
2 and a thickness T, was subjected to thermogravimetric analysis (TGA) by heating from
room temperature to 800°C at a speed of 10°C/minute in the air, to determine the amount
of residual carbon per a unit volume. As a result, the amount of carbon remaining
in the coating layer was 100 mg/cm
3.
(c) Measurement of hardness
[0049] The hardness of the coating layer was measured by a self-hardening mold hardness
tester (NK-009 available from Nakayama Co., Ltd.) at five points, and averaged. As
a result, the hardness of the coating layer on the recess was 67.
(5) Mold-combining step
[0050] The upper and lower mold parts provided with coating layers on recesses and parting
surfaces were combined by a usual method to obtain a green sand mold.
[0051] A melt having a composition comprising 0.45% by mass of C, 1.30% by mass of Si, 1.02%
by mass of Mn, 10.1% by mass of Ni, 19.9% by mass of Cr, 10.0% by mass ofNb, 0.15%
by mass of S, and 0.18% by mass ofN, the balance being Fe and inevitable impurities,
was poured at 1620-1630°C into a cavity of the above green sand mold. After the solidification
of the melt, the green sand mold was broken to take a cast steel article, from which
casting sand attached to its as-cast surface was removed by shot-blasting for 15 minutes
using steel balls of 2.4 mm in average diameter. Likewise, totally 100 cast steel
articles were produced.
(a) Measurement of sand seizure ratio
[0052] Sand seizure on the shot-blasted as-cast surface was observed with the naked eye,
and the number of cast steel articles suffering sand seizure was divided by the total
number (100) of cast steel articles to determine the sand seizure ratio (%). As a
result, the sand seizure ratio was 1%.
(b) Measurement of surface defect ratio
[0053] The surface defects of the cast steel article, such as pinholes generated by insufficient
gas evacuation, burr generated by the cracking and breakage of the coating layer on
the recess, etc., were observed with the naked eye. The number of cast steel articles
suffering surface defects was divided by the total number (100) of cast steel articles,
to determine the surface defect ratio (%). As a result, the surface defect ratio was
2%.
(c) Evaluation of machinability
[0054] To evaluate the machinability of an as-cast surface of a cast steel article, a surface
layer (depth range: 1.0 mm including the as-cast surface) of the cast steel article
was cut by milling with a cemented carbide insert PVD-coated with TiAlN, under the
following conditions:
Cutting speed: 150m/minute,
Cutting depth: 1.0 mm,
Feed per blade: 0.2 mm/blade,
Feed speed: 381 mm/minute,
Rotation speed: 76 rpm, and
Cutting liquid: No (dry).
[0055] A cutting time until the wear of a cemented carbide insert flank became 0.2 mm or
more was judged as a tool life, as a parameter of machinability. With the tool life
(machinability) in Comparative Example 1 being 100, the machinability in Example 1
was 126.
Example 2
[0056] 100 cast steel articles were produced in the same manner as in Example 1, except
for changing (a) the ratio of a phenol in the coating solution to 30% by mass, (b)
the viscosity and amount of the coating solution to 17 mPa·s and 100 g/m
2, respectively, and (c) the coating-layer-forming conditions, to form a coating layer
having hardness of 50 and a thickness T of 2.3 mm, the amount of residual carbon being
22 mg/cm
3, on the recess. The same measurements of machinability, a sand seizure ratio and
a surface defect ratio as in Example 1 revealed that the machinability was 133, the
sand seizure ratio was 3%, and the surface defect ratio was 3%.
Example 3
[0057] 100 cast steel articles were produced in the same manner as in Example 1, except
for forming a coating layer having hardness of 50 and a thickness T of 1.7 mm, the
amount of residual carbon being 50 mg/cm
3, on the recess by (a) a phenol ratio of 20% by mass in the coating solution, (b)
a coating solution viscosity of 13 mPa·s, and (c) the two-step hardening of the coating
layer. The two-step hardening comprised a first hardening step of forming a semi-hardened
layer having hardness of 36, the combining of the mold parts, and a second hardening
step of further heating to completely harden the semi-hardened layer. The same measurements
of machinability, a sand seizure ratio and a surface defect ratio as in Example 1
revealed that the machinability was 130, the sand seizure ratio was 2%, and the surface
defect ratio was 4%.
Examples 4-6
[0058] 100 cast steel articles were produced in the same manner as in Example 1, except
for changing the ratio of a phenol in the coating solution and the amount of the coating
solution applied as shown in Table 2. The machinability, sand seizure ratio and surface
defect ratio of the cast steel article of each Example were measured in the same manner
as in Example 1. In Example 4, the machinability was 113, the sand seizure ratio was
1%, and the surface defect ratio was 4%. In Example 5, the machinability was 109,
the sand seizure ratio was 1%, and the surface defect ratio was 3%. In Example 6,
the machinability was 118, the sand seizure ratio was 2%, and the surface defect ratio
was 2%.
Comparative Example 1
[0059] 100 cast steel articles were produced in the same manner as in Example 1, except
for changing the ratio of carbon powder in the casting sand to 4.0 parts by mass.
The same measurements of machinability, a sand seizure ratio and a surface defect
ratio as in Example 1 revealed that the machinability was 100, the sand seizure ratio
was 3%, and the surface defect ratio was 11%.
Comparative Example 2
[0060] 100 cast steel articles were produced in the same manner as in Comparative Example
1, except for changing the ratio of a phenol in the coating solution and the amount
of the coating solution applied as shown in Table 2. The same measurements of machinability,
a sand seizure ratio and a surface defect ratio as in Example 1 revealed that the
machinability was 92, the sand seizure ratio was 1%, and the surface defect ratio
was 35%.
Comparative Example 3
[0061] 100 cast steel articles were produced in the same manner as in Example 1, except
for changing the ratio of a phenol in the coating solution and the amount of the coating
solution applied as shown in Table 2. The same measurement of machinability, a sand
seizure ratio and a surface defect ratio as in Example 1 revealed that the machinability
was 72, the sand seizure ratio was 23%, and the surface defect ratio was 10%. The
deterioration of machinability appears to be due to the sand seizure of an as-cast
surface.
[0062] With respect to Examples 1-6 and Comparative Examples 1-3, the production conditions
of green sand molds are shown in Table 1, and the composition, viscosity and amount
of a coating solution applied to each green sand mold, as well as the hardness, thickness
and residual carbon content of each coating layer are shown in Table 2. Also, the
evaluations of machinability, sand seizure ratio and surface defect ratio of their
cast steel articles, and their overall evaluations are shown by three grades in Table
3.
Machinability (expressed by a relative value to 100 in Comparative Example 1)
[0063]
Excellent: 120 or more.
Good: more than 100 and less than 120.
Poor: 100 or less.
Sand seizure ratio
[0064]
Excellent: 2% or less.
Good: more than 2% and less than 10%.
Poor: 10% or more.
Surface defect ratio
[0065]
Excellent: 2% or less.
Good: more than 2% and less than 10%.
Poor: 10% or more.
Overall evaluation
[0066]
Excellent: All evaluations of machinability, sand seizure ratio and surface defect
ratio were excellent.
Good: Any one of evaluations of machinability, sand seizure ratio and surface defect
ratio was good.
Poor: Any one of evaluations of machinability, sand seizure ratio and surface defect
ratio was poor.
Table 1
No. |
Production conditions of Green Sand Mold |
Casting Sand |
Hardness(1) of Formed Recesses |
Bentonite |
Water |
Carbonaceous Component |
Type |
Ratio |
Example 1 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Example 2 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Example 3 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Example 4 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Example 5 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Example 6 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Com. Ex. 1 |
8.1 |
3 |
Carbon Powder |
4 |
20 |
Com. Ex. 2 |
8.1 |
3 |
Carbon Powder |
4 |
20 |
Com. Ex. 3 |
8.1 |
3 |
Carbon Powder |
3 |
20 |
Note: (1) Average hardness of recesses (with no coating) of the formed upper and lower
mold parts. |
Table 2-1
No. |
Thermosetting Resin |
Coating Solution |
Number of Hardening Steps |
Type |
% by mass |
Viscosity (mPa·s) |
Applied Amount (g/m2) |
Example 1 |
Ph(1) |
40 |
20 |
300 |
1 |
Example 2 |
Ph(1) |
30 |
17 |
100 |
1 |
Example 3 |
Ph(1) |
20 |
13 |
300 |
2(2) |
Example 4 |
Ph(1) |
70 |
100 |
340 |
1 |
Example 5 |
Ph(1) |
50 |
45 |
500 |
1 |
Example 6 |
Ph(1) |
22 |
15 |
500 |
1 |
Com. Ex. 1 |
Ph(1) |
40 |
20 |
300 |
1 |
Com. Ex. 2 |
Ph(1) |
80 |
140 |
550 |
1 |
Com. Ex. 3 |
Ph(1) |
5 |
10 |
200 |
1 |
Note: (1) Phenol.
(2) The thermosetting resin was thermally cured by the first and second hardening
steps, and the surface hardness of the recess after the first hardening step was 36. |
Table 2-2
No. |
Coating Layer |
Surface Hardness(1) |
Thickness T (mm) |
Residual Carbon (mg/cm3) |
Example 1 |
67 |
1.1 |
100 |
Example 2 |
50 |
2.3 |
22 |
Example 3 |
50 |
1.7 |
50 |
Example 4 |
80 |
0.5 |
198 |
Example 5 |
95 |
0.9 |
208 |
Example 6 |
69 |
2.3 |
92 |
Com. Ex. 1 |
67 |
1.1 |
100 |
Com. Ex. 2 |
98 |
0.4 |
360 |
Com. Ex. 3 |
36 |
2.8 |
8 |
Note: (1) Surface hardness of recesses. |
Table 3
No. |
Properties of Products |
Machinability |
Sand Seizure Ratio |
Surface Defect Ratio |
Overall Evaluation |
Example 1 |
Excellent |
Excellent |
Excellent |
Excellent |
Example 2 |
Excellent |
Good |
Good |
Good |
Example 3 |
Excellent |
Excellent |
Good |
Good |
Example 4 |
Good |
Excellent |
Good |
Good |
Example 5 |
Good |
Excellent |
Good |
Good |
Example 6 |
Good |
Excellent |
Excellent |
Good |
Com. Ex. 1 |
Poor |
Good |
Poor |
Poor |
Com. Ex. 2 |
Poor |
Excellent |
Poor |
Poor |
Com. Ex. 3 |
Poor |
Poor |
Poor |
Poor |
[0067] In Examples 1-6, with the ratio of a carbonaceous component in the green sand mold,
and the surface hardness of the coating layer adjusted as described above, cast steel
articles with good or excellent machinability, and good or excellent sand seizure
ratios and surface defect ratios as shown in Table 3 were obtained. On the other hand,
in Comparative Examples 1-3, in which the ratio of a carbonaceous component in the
green sand mold and the surface hardness of the coating layer were outside the ranges
of the present invention, the resultant cast steel articles were poor in one or more
of machinability, a sand seizure ratio and a surface defect ratio.
DESCRIPTION OF REFERENCE NUMERALS
[0068]
1: Green sand mold
1a: Upper mold part
1b: Lower mold part
1c: Article-forming cavity
1d: Runner
1e: Parting surface
1f: Coating layer
1g-1, 1g-2: Recess
1i: Void
1j: Sand particle
1k: Coating solution
1L: Semi-hardened layer
M: Melt