[0001] The object of the present invention is powder composition for the manufacture of
casting inserts used in the fabrication of wear-resistant local composite zones; another
object of the present invention is casting insert, the use of which allows increasing
the resistance to abrasive wear in cast parts of machines operating under conditions
of heavy mechanical loads. The present invention also provides a method for the fabrication
of local composite zones in castings, wherein said local composite zones increase
the resistance of castings to the degradation process and the resistance to abrasive
wear of machinery operating under conditions of heavy mechanical loads.
[0002] In the technology of making castings, which in selected areas are characterized by
increased resistance to shock and abrasion, the process of
in situ synthesis of the silicon carbide SiC uses the method of Self-Propagating High Temperature
Synthesis (SHS). The process of the synthesis of titanium carbide TiC is well known
in the field of classical powder metallurgy. Equally well known are the problems concerning
the control of the SHS reaction, wherein said reaction once initiated is a self-sustained
process, which means that the amount of heat generated by the reaction can further
spread out this reaction. Fading of the reaction can occur only then, when the heat
volume dissipated by the system is larger than the heat volume generated during the
reaction.
[0003] As regards casting processes, well-known is the method disclosed in U.S. Patent
US2011/0226882A1, by means of which local composite reinforcements are fabricated in the cast parts
of machines and equipment. The disclosed method involves placing in mould cavity the
shaped inserts or granules of reactants responsible for the formation of titanium
carbide TiC, which are next poured with molten iron-based alloy. The heat supplied
by molten alloy initiates the reaction of the synthesis of titanium carbide TiC. The
in situ process of the synthesis taking place in molten alloy is governed by the physical
phenomena occurring in liquids. This applies, in particular, to the reactive infiltration
assisted by capillary phenomena, intensified by a high temperature of the alloy cast
and by a high value of the heat generated during the reaction of the synthesis of
titanium carbide TiC. After initiation of the reaction of synthesis, the crystals
of titanium carbide TiC nucleating and growing in molten alloy can build bridges and
undergo coalescence. However, said reactive infiltration results in spreading of molten
alloy between the nucleating and growing crystals or coagulated particles of TiC.
As a consequence, particles or crystals of titanium carbide TiC are separated by the
liquid. Since the crystals or particles of titanium carbide TiC are exposed to the
effect of the force of buoyancy caused by different densities of the molten iron-based
alloy and titanium carbide, the result is an uneven distribution of said elements
in casting. This can lead to fragmentation of the composite zone, which is an obstacle
to the formation of an effective local composite reinforcement in the casting. Particularly
undesirable in castings is the devastating effect of crack propagation. Cracks in
the cast material are initiated by microcracks, which can occur in those areas of
the casting where the most brittle phase of the material is located, said phase being
in this case composed of the particles of titanium carbide TiC. It is therefore advantageous
and desirable that the brittle areas composed of titanium carbide TiC were thoroughly
separated from each other by a metallic matrix material, since any larger amount of
the metallic matrix material present between the particles of titanium carbide TiC
will arrest further propagation of these brittle areas.
[0004] U.S. Patent
US 20110303778A1 discloses a process which reduces the phenomenon of crack propagation. The aim has
been achieved through the use of material characterized by a hierarchical structure,
wherein the reinforced phase comprises, spread in a ferrous alloy, millimetric granules
containing micrometric coagulated particles of titanium carbide TiC, and wherein the
areas between the particles of titanium carbide TiC are also filled with a ferrous
alloy. In order to achieve the structure shown, previously prepared granules of compressed
powders of Ti and C are placed in selected areas of casting mould, and are prevented
from being dispersed by separating means, and then the mould is poured with a ferrous
alloy. The granulated composite structure allows controlling the size of the areas
with clusters of titanium carbide TiC and partial control of the distance between
these clusters. Additionally, it also facilitates the removal of gases formed during
the SHS synthesis, which reduces the number of pores in casting. On the other hand,
the granular structure does not provide sufficient resistance of the material to abrasive
wear. Large distances between the granules with particles of titanium carbide TiC
are not preferred, since they facilitate the erosion process in the infiltrating material,
and this, in turn, promotes chipping of the agglomerates of titanium carbide TiC.
Hence the target is to develop a composite structure that will resist the effect of
crack propagation and also the effect of erosion.
[0005] In the manufacture of modern parts of machines and equipment made by the technique
of casting, the target is to seek new simplified methods for the fabrication of local
zones of increased strength and resistance to abrasive wear, thus improving further
the durability of cast parts of said machines and equipment, allowing simultaneously
for a convenient and easy application of these methods without the need to use any
additional devices. The essence of the present invention is a powder composition for
the fabrication of casting inserts designed to produce local composite zones resistant
to abrasive wear, wherein said composite zones are reinforced with carbides and borides
formed
in situ in castings, and wherein said powder composition is characterized in that it comprises
powder reactants of the formation of carbides and/or borides selected from the group
of TiC, WC, ZrC, NbC, TaC, TiB
2, ZrB
2, or mixtures thereof, said carbides and/or borides forming after crystallization
particles reinforcing the composite zones in castings, and wherein said powder composition
further comprises moderator powders in the form of a mixture of metal powders which
after crystallization form matrix of the composite zone in casting.
[0006] Preferably, the amount of powder reactants of the titanium carbide TiC formation
in the composition according to the invention is from 3 to 40wt% and the amount of
moderator powders is from 60 to 97wt%.
[0007] Also preferably, the amount of powder reactants of the tungsten carbide WC formation
in the composition according to the invention is from 40 to 99wt% and the amount of
moderator powders is from 1 to 60wt%.
[0008] Also preferably, the amount of the mixture of powder reactants of the coupled reaction
of the formation of titanium carbide TiC and tungsten carbide WC in the composition
according to the invention is from 10 to 70wt% and the amount of moderator powders
is from 30 to 90wt%.
[0009] Also preferably, the powder reactants of the formation of carbides and/or borides
have particles of the size of up to 100 □m, but preferably not larger than 45 □m.
[0010] Preferably, the moderator powders additionally comprise a non-metal in the form of
C.
[0011] Preferably, carbon as a reactant powder takes the form of graphite, amorphous graphite,
a carbonaceous material or mixtures thereof, and in the case of Ti, W, Zr, Nb, Ta
these are powders of pure metals or powders of alloys of these metals with other elements,
or mixtures thereof.
[0012] Preferably, moderator powders from the group of metals consist of a powder selected
from the group of Fe, Co, Ni, Mo, Cr, W, Al, or of a mixture of said powders. In particular,
preferably, the moderator powders further comprise at least one powder selected from
the group of Mn, Si, Cu, B, or a mixture thereof.
[0013] Also preferably, the moderator powders have the chemical composition of an alloy
selected from the group comprising grey cast iron, white cast iron, chromium cast
iron, cast chromium steel, cast unalloyed steel, cast low-alloy steel, cast Hadfield
manganese steel or Ni-Hard4 chromium cast iron containing Ni.
[0014] In another embodiment of the composition according to the invention, the moderator
powder is a mixture of powders selected from the group of: (a) Fe, Cr, Mn, Si, Mo,
C; (b) Fe, Cr, Mn, Si, C; (c) Co, Cr, W, C; (d) Co, Fe, Ni, Mo, Cr, C; (e) Ni, Cr,
Mo, Nb, Al, Ti, Fe, Mn, Si; (f) Ni, Cr, Co, W, Nb, Al, Ti, C, B, Zr; (g) Co, Ni, Fe.
[0015] Preferably, the moderator powders also include powders of ceramic phases increasing
the resistance to wear, in particular powders selected from the group of ZrO
2, stabilized ZrO
2, Al
2O
3, or a mixture thereof, and/or a reducing component in the form of Al and/or Si, wherein
the amount of the reducing component in the powder composition is maximum 5wt%.
[0016] The essence of the present invention is also a casting insert to produce wear-resistant
local composite zones in castings, wherein said casting insert comprises the reactants
of the carbide and/or boride formation, and wherein said casting insert is in the
form of shapes, solids, preforms or granules, and is characterized in that it comprises
a compacted powder composition according to the invention.
[0017] In yet another embodiment, the invention also relates to a method for producing local
composite zones in castings, involving the reaction of self-propagating high temperature
synthesis (SHS), wherein a powder mixture comprising the reactants of the carbide
and/or boride formation is prepared, said powder mixture being next subjected to compaction,
conferring to the compacted powder mixture the form of particular shapes, solids,
preforms or granules which serve as casting inserts, placing next at least one casting
insert in the interior of the mould, and pouring next said mould with molten casting
alloy in an amount sufficient to initiate the SHS reaction, and wherein said invention
is characterized in that a powder mixture comprising the reactants of the carbide
and\or boride formation is prepared, said powder mixture making powder composition
according to the invention.
[0018] Preferably, the prepared powder mixture is dried, preferably at a temperature of
200°C until the content of moisture is maximum 2%.
[0019] Preferably, the operation of compaction is performed under a pressure ranging from
450 MPa to 650 MPa.
[0020] Preferably, the casting insert is placed in the mould cavity in a predetermined position
and is fixed to the mould with bolts or is placed on a steel frame, said frame being
placed inside the mould cavity, wherein preferably the steel frame consists of rods
onto which the compacts having the holes are threaded.
[0021] Owing to the use of moderator, the composite zones produced
in situ in castings are characterized by stable and predictable size, and crystals of titanium
carbide TiC have similar submicron dimensions. The presence of a large number of the
fine crystals of titanium carbide TiC of a relatively uniform distribution imparts
to the composite zone an improved abrasive wear resistance and also an improved impact
strength, as in the vicinity of fine crystals the mechanical stress is reduced, while
smaller distances between these crystals increase the resistance of the composite
zone to erosion.
[0022] The method according to the present invention provides a much more precise control
of the SHS process during casting. As already mentioned, the typical SHS process is
a self-sustained reaction, which once initiated proceeds rapidly until all the input
material is reacted. Since the reaction is highly exothermic and results in a rapid
increase of temperature combined with the emission of gases, there is an imminent
risk of the formation of cavities and pores. In an embodiment according to the present
invention, through careful selection of the composition of the moderator, wherein
said moderator composition not only has the ability to effectively absorb the excess
heat but has also the ability to increase hardness and wear resistance of the composite
matrix, and additionally has the ability to absorb gases, the aforementioned drawbacks
have been minimized.
[0023] The invention also relates to a casting insert fabrication method using a composition
of powders designed to produce local composite zones resistant to abrasive wear, wherein
said composite zones reinforced with carbides and borides, or with mixtures thereof,
are formed in situ in castings, and wherein said composition of powders comprises
powder reactants of the formation of carbides selected from the group of TiC, WC,
or mixtures thereof, wherein said carbides or borides after crystallization form particles
reinforcing the composite zones in castings, and moderator powders forming a mixture
of metal powders, wherein said metal powders after crystallization form matrix of
the composite zone in casting, wherein the amount of powder reactants for the formation
of TiC carbide is from 3 to 40wt% and the amount of moderator powders is from 60 to
97wt%, the amount of powder reactants for the formation of WC carbide is from 40 to
99wt% and the amount of moderator powders is from 1 to 60wt%, or the amount of the
mixture of powders for the reactants of the coupled reaction of the synthesis of TiC
and WC carbides is from 10 to 70wt% and the amount of moderator powders is from 30
to 90wt%.
[0024] Preferably, the powders of the reactants of the formation of carbides have particles
of the size of up to 100 µm, but preferably not larger than 45 µm.
[0025] Preferably, the carbon as a powder reactant is in the form of graphite, amorphous
graphite, a carbonaceous material or a mixture thereof, and in the case of Ti, or
W, these are the powders of pure metals or alloys of said metals with other elements,
or mixtures thereof.
[0026] Preferably, the moderator powders additionally comprise a non-metal in the form of
carbon.
[0027] Preferably, the moderator powders from the group of metals comprise any powder selected
from the group of Fe, Co, Ni, Mo, Cr, W, Al, or comprise a mixture of said powders.
[0028] Preferably, the moderator powders further comprise at least one powder selected from
the group of Mn, Si, Cu, B, or a mixture of said powders.
[0029] Preferably, the moderator powders have the chemical composition of an alloy selected
from the group of grey cast iron, white cast iron, chromium cast iron, cast chromium
steel, cast unalloyed steel, cast low-alloy steel, cast Hadfield manganese steel,
or Ni-Hard4 chromium cast iron containing Ni.
[0030] Preferably, the moderator powder is a mixture of powders selected from the group
of: (a) Fe, Cr, Mn, Si, Mo, C; (b) Fe, Cr, Mn, Si, C; (c) Co, Cr, W, C; (d) Co, Fe,
Ni, Mo, Cr, C; (e) Ni, Cr, Mo, Nb, Al, Ti, Fe, Mn, Si; (f) Ni, Cr, Co, W, Nb, Al,
Ti, C, B, Zr; (g) Co, Ni, Fe.
[0031] Preferably, the moderator powders also include phases of ceramic powders increasing
the resistance to wear, in particular the phases of ceramic powders selected from
the group of ZrO
2, stabilized ZrO
2, Al
2O
3or a mixture thereof; and/or a reducing component in the form of Al and/or Si, wherein
the amount of the reducing component is maximum 5wt% of the powder composition.
[0032] According to another aspect of the invention, there is provided a casting insert
for the fabrication of local composite zones resistant to wear, comprising reactants
of the carbide formation, wherein said insert in the form of shapes, solids, preforms
or granules wherein in it is fabricated by a casting insert fabrication method according
to any one of the aspects detailed above.
[0033] According to another aspect of the invention, there is provided a method for the
fabrication of local composite zones in castings, which uses the reaction of self
-propagating high-temperature synthesis (SHS), said method comprising a preparation
of a powder mixture, wherein said mixture comprises reactants of carbide formation,
and wherein said mixture is next compacted conferring to the compacted powder composition
a particular form, especially of shapes, solids, preforms or granules forming a casting
insert, and wherein at least one casting insert is next placed in an interior of a
mould, and said mould is poured with molten casting alloy in an amount sufficient
to initiate the SHS reaction, and wherein said method is further characterized in
that the casting insert is fabricated by a method according to any one of aspects
detailed above.
[0034] Preferably, after preparing the powder mixture, said mixture is dried, preferably
at 200°C, until the moisture content is maximum 2%.
[0035] Preferably, the operation of compaction is performed under a pressure ranging from
450 MPa to 650 MPa.
[0036] Preferably, the casting insert is placed in a mould cavity in a predetermined position
and is fixed to the mould with bolts or is placed on a steel frame, said frame being
placed inside the mould cavity, wherein preferably the steel frame consists of rods
on which compacts having holes are threaded
[0037] Within the description of the invention and patent claims, the following terms shall
be construed as defined below:
The term "
metal powder" is intended to mean any metal in any form disintegrated to powder by any arbitrary
method.
[0038] The term "m
oderator" is intended to mean a mixture of metal powders, said mixture optionally containing
also non-metals, wherein said metal powders during the reaction of the SHS synthesis
of selected carbide or of a mixture of carbides undergo melting and form a matrix
of the composite zone. The fundamental role of moderator introduced to the reactants
of the formation of a compound undergoing the SHS reaction is to reduce the amount
of dissipated energy, which is possible due to the replacement of a part by weight
of the reactants with said moderator. The task of the moderator is therefore to reduce
the reactive infiltration, which occurs during the highly exothermic SHS synthesis
of selected ceramic phase, and along with the reactive infiltration to reduce also
the adverse phenomenon known as destructive fragmentation of the
in situ generated composite zones. An additional task of the moderator is to reduce the size
of particles formed as a result of the reaction of the SHS synthesis, which is achieved
through the moderator impact on the crystallization process of the particles. The
presence of the moderator also results in a relatively uniform distribution of particles
within the composite zones and increases hardness and wear resistance of these zones.
[0039] The term "
ceramic moderator" is intended to mean a ceramic powder, preferably of ZrO
2 and/or Al
2O
3, which is incorporated to increase the abrasive wear resistance of composite zones,
to control the phenomenon of reactive infiltration and to reduce the adverse effect
of total fragmentation.
[0040] The term "r
educing component" is intended to mean an addition of powder, preferably of Al and/or Si, incorporated
in order to bind the atoms of gas released during the reaction of the SHS synthesis
proceeding in casting within the
in situ generated composite zones and also to reduce or eliminate the defects in the form
of porosity.
[0041] The term "c
asting insert " is intended to mean a densified powder composition, incorporated in order to produce
in situ in casting the composite zones reinforced with carbides and/or oxides, a key element
in said casting insert being the addition of a moderator. The moderator present in
the casting insert prevents the occurrence of an adverse phenomenon of the fragmentation
of composite zones, resulting in that said zones are broken into pieces and can move
in molten alloy poured into the mould cavity. The casting insert can assume the shape
of any arbitrary solid body or preform, or it can be used in the form of granules.
It is placed in mould cavity and should be fixed therein in such a way as to prevent
its movement in the casting during pouring of the mould cavity.
[0042] The term "
base alloy" is intended to mean a casting alloy which is poured into the mould cavity with the
casting insert disposed in the interior of said mould cavity to produce the composite
zones in casting.
[0043] The object of the present invention is now explained in the embodiments that do not
limit its scope and in the drawings, wherein:
Fig. 1 shows the sequential steps of a method for producing composite zones in castings,
including a mould cavity wherein the casting inserts are placed (a), a method for
fixing said casting inserts in position (b), composite zones visible in the milled
cross-section of the bottom part of casting (c), and in the milled cross-section of
the upper part of casting, the latter one showing scattered fragments of said composite
zones produced from casting inserts containing the reactants of titanium carbide (TiC)
formation and less than 50wt% of a moderator powder in the form of cast Hadfield high-manganese
steel with 21wt% Mn (d);
Fig. 2 shows a mould cavity wherein the casting inserts are placed (a), and a polished
cross-section of the casting (b), when the composite zones are fabricated from materials
containing the reactants of titanium carbide (TiC) formation and a moderator powder
in the form of pure iron;
Fig. 3 shows a mould cavity wherein the casting inserts are placed (a), a milled cross-section
of the casting (b), and a polished cross-section of the casting (c), when the composite
zones are fabricated from materials containing the reactants of titanium carbide (TiC)
formation and a moderator powder in the form of cast Hadfield high-manganese steel
with 21wt% Mn;
Fig. 4 shows a mould cavity wherein the casting inserts are placed (a), a milled cross-section
of the casting (b), and a polished cross-section of the casting (c), when the composite
zones are fabricated from materials containing the reactants of titanium carbide (TiC)
formation and a moderator powder in the form of Ni-Hard4 chromium cast iron containing
Ni;
Figure 5 shows a mould cavity wherein the casting inserts are placed (a), and a polished
cross-section of the casting (b), when the composite zones are fabricated from materials
containing the reactants of tungsten carbide (WC) formation and a moderator powder
in the form of Ni-Hard4 chromium cast iron containing Ni;
Fig. 6 shows a mould cavity wherein the casting inserts are placed (a), and polished
cross-sections of the casting (b-c), when the composite zones are fabricated from
materials containing the reactants of the coupled formation of titanium carbide and
tungsten carbide (TiC, WC) and a moderator powder in the form of Ni-Hard4 chromium
cast iron containing Ni;
Fig. 7-9 show microstructure in a cross-section of the transition region located between
the composite zone and the rest of casting and microstructure of the composite zone,
wherein said microstructure depends on the composition of a powder mixture used for
the fabrication of casting inserts, including the amount of moderator;
Fig. 10 shows a general flow chart of a method for producing local composite zones
in castings according to the invention;
Fig. 11-16 show the relationship between changes in the hardness of composite zones
produced in situ in the casting and composition of the powder mixture used for the manufacture of
casting inserts, including the weight content of moderator incorporated in said powder
mixture used for the manufacture of said inserts.
[0044] The present invention is now illustrated by the following examples of its embodiments.
Example 1
[0045] In Example 1, the mould cavity and casting inserts were prepared for the fabrication
of composite zones reinforced with TiC carbide (Fig. 1a), including the operation
of fixing said casting inserts by means of an assembly system in said mould cavity
(Fig. 1b). The casting inserts were made from a powder mixture comprising the reactants
of TiC formation and a moderator having the composition of cast high-manganese steel
containing 21% Mn. The composition of the powder mixture used for the fabrication
of casting inserts and the obtained results are included in Table 1. Symbols "+" and
"-" in Tables 1-6 stand for the answers "yes" and "no", respectively, in a schematic
description of the results of examinations of the polished cross-section of a casting
with the composite zones fabricated by an
in situ method. The chemical composition of a moderator in the form of cast Hadfield high-manganese
steel is given in Table 8.
Table 1
Sample No. |
A1 |
A2 |
A3 |
A4 |
A5 |
A6 |
Reactants of TiC formation [wt%] |
100 |
90 |
70 |
50 |
30 |
10 |
Moderator having the composition of cast Hadfield high-manganese steel with 21% Mn
[wt%] |
0 |
10 |
30 |
50 |
70 |
90 |
The visibility of composite zones |
- |
- |
- |
+ |
+ |
+ |
Total fragmentation of composite zone |
+ |
+ |
+ |
- |
- |
- |
Partial fragmentation of composite zone |
- |
- |
- |
+ |
- |
- |
The content of macroporosity and fragments of composite zone in the upper part of
casting |
+ |
+ |
+ |
- |
- |
- |
[0046] In the first experiment, casting inserts were fixed in the mould cavity to produce
composite zones reinforced with titanium carbide TiC, as shown in Figures 1a and 1b.
The inserts contained various amounts of the moderator in the form of a powder mixture
having the composition of cast Hadfield high-manganese steel with 21wt% Mn and reactants
of the titanium carbide TiC formation. The atomic ratio of the reactants was 50at%
Ti : 50 at% C. The inserts were made by compaction under a pressure of 600 MPa and
had dimensions of 20 ×100 × X mm, where X for individual inserts was from 8 to 15
mm, respectively. Next, a 6 kg weighing casting measuring 70 × 150 × 150 mm was made
from the L35GSM steel and had the composite zones visible in Figure 1c formed
in situ from the casting inserts containing 50wt%, 70wt% and 90wt% of the moderator addition
in zones A4 to A6, respectively, whereas the composite zones formed
in situ from the casting inserts containing 0wt%, 10wt% and 30wt% of the moderator addition
were scattered and invisible (the area marked with symbols A1 to A3 in Figure 1c).
Fragments of the scattered composite zones are visible in the milled upper casting
surface shown in Figure 1d.
[0047] The composite zones produced without the addition of moderator and with the addition
of moderator in an amount of 10wt% and 30wt% (compacts A1, A2 and A3, respectively,
Table 1) have undergone the process of fragmentation (Fig. 1c) with a significant
share of macroporosity and fragments of composite layer present in the upper part
of casting (Fig. 1d). This macrostructure was the result of intense infiltration induced
by a significant increase in temperature during the reaction of the SHS synthesis
of titanium carbide TiC caused by the absence of moderator. Since the reaction of
synthesis is highly exothermic, the significant increase in temperature promotes the
process of infiltration as well as the production and dissolution of gases. As a result,
stable composite zones are not obtained in the casting; instead only randomly distributed
fragments of these zones containing TiC carbide are present. With the growing percent
content of moderator addition having the composition of cast high-manganese steel
with 21% Mn, the tendency towards dimensional stabilization starts prevailing and
macroporosity defects disappear in respective zones. As shown in Figures 1 and 2,
at 70wt% content of the moderator, the macroscopically optimal dimensional stability
and the lowest fraction of macroporosity are obtained in castings. Using this moderator,
the relative dimensional stability is obtained only in those zones in which the percent
content of the moderator powder exceeds 50wt%. The, visible in Figure 1d, top surface
of the casting shows fragments of composite zones obtained with the moderator addition
of 0wt%, 10wt%, 30wt%, wherein said composite zones during the
in situ reaction of TiC synthesis in molten alloy have undergone the process of fragmentation
and floated to the top. This effect was observed in a series of 15 tests. The results
of experimental studies have also indicated that when the casting inserts for the
in situ fabrication of composite zones in castings contain only powder reactants of the TiC
synthesis, local composite zones are not formed due to the disadvantageous phenomenon
of the fragmentation of these zones.
[0048] In the second experiment, the mould cavity and casting inserts were prepared for
the fabrication of composite zones reinforced with TiC carbide (Fig. 2a), including
the operation of fixing said casting inserts by means of an assembly system in said
mould cavity. The casting inserts were made from a powder mixture comprising the reactants
of TiC formation and a moderator having the composition of pure Fe powder added in
the amounts as indicated in Table 2. The composition of the powder mixture used for
the fabrication of casting inserts and the obtained results are included in Table
2. The atomic ratio of the reactants was 55at% Ti : 45at% C. The inserts were made
by compaction under a pressure of 500 MPa and had dimensions of 20 × 50× X mm, where
X for individual inserts was from 15 to 25 mm, respectively.
Table 2
Sample No. |
B1 |
B2 |
B3 |
B4 |
B5 |
B6 |
B7 |
B8 |
B9 |
Reactants of TiC formation [wt%] |
100 |
90 |
70 |
50 |
40 |
30 |
20 |
10 |
3 |
Moderator having the composition of pure Fe powder [wt%] |
0 |
10 |
30 |
50 |
60 |
70 |
80 |
90 |
97 |
The visibility of composite zones |
- |
- |
- |
+ |
+ |
+ |
+ |
+ |
+ |
Total fragmentation of composite zone |
+ |
+ |
+ |
- |
- |
- |
- |
- |
- |
Partial fragmentation of composite zone |
- |
- |
- |
+ |
- |
- |
- |
- |
- |
The content of macroporosity and fragments of composite zone in the upper part of
casting |
+ |
+ |
+ |
- |
- |
- |
- |
- |
- |
[0049] In the third experiment, casting inserts to produce the composite zones reinforced
with TiC carbide were fixed in the mould cavity, as shown in Figure 3a. The inserts
contained various amounts of the moderator powder having the composition of cast high-manganese
steel with 21wt% Mn. The composition of the powder mixture used for the fabrication
of casting inserts and the obtained results are included in Table 3. The atomic ratio
of the reactants was 55at% Ti : 45at% C. The inserts were made by compaction under
a pressure of 500 MPa and had dimensions of 20 × 50 × X mm, where X for individual
inserts was from 15 to 25 mm, respectively. Then, in a 7 kg weighing casting made
from the L450 steel with dimensions of 43 × 70 × 250 mm and a wall thickness of 48
mm, two cross-sections were prepared by milling (Fig. 3b) and polishing (Fig. 3c).
In both cross-sectional areas are visible the composite zones fabricated
in situ from the casting inserts containing 50wt%, 60wt%, 70wt% A, 70wt% B, 80wt%, 90wt%
and 97wt% of the moderator addition in samples C3-C8, respectively, whereas composite
zones containing10wt% and 30wt% of the moderator addition in samples C1-C2, respectively,
are dispersed and invisible because of the total fragmentation effect taking place
in casting. The zone produced with 50wt% of the moderator addition has undergone partial
fragmentation, as proved by the presence of molten alloy penetrating into the zone
and splitting it into smaller fragments.
Table 3
Sample No. |
C1 |
C2 |
C3 |
C4 |
C5 |
C6 |
C7 |
C8 |
C9 |
Reactants of TiC formation [wt%] |
90 |
70 |
50 |
40 |
30A |
30B |
20 |
10 |
3 |
Moderator having the composition of cast Hadfield high-manganese steel with 21% Mn
[wt%] |
10 |
30 |
50 |
60 |
70A |
70B |
80 |
90 |
97 |
The visibility of composite zones |
- |
- |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
Total fragmentation of composite zone |
+ |
+ |
- |
- |
- |
- |
- |
- |
- |
Partial fragmentation of composite zone |
- |
- |
+ |
- |
- |
- |
- |
- |
- |
The content of macroporosity and fragments of composite zone in the upper part of
casting |
+ |
+ |
- |
- |
- |
- |
- |
- |
- |
[0050] In the fourth experiment, the powder compositions were tested for the fabrication
of local composite zones reinforced with TiC carbide, which contained the addition
of moderator in the form of a powder mixture having the composition of Ni-Hard4 chromium
cast iron containing Ni. The composition of the powder mixture used for the fabrication
of casting inserts and the obtained results are included in Table 4. The atomic ratio
of the reactants was 55wt%Ti : 45at%C. The inserts were made by compaction under a
pressure of 500 MPa and had dimensions of 20 × 50 × X mm, where X for individual inserts
was from 15 to 25 mm, respectively. The casting inserts were fixed in the mould cavity
as shown in Figure 4a. The mould cavity with the casting inserts fixed therein was
poured with the L450 alloy having the composition as shown in Table 8. In this way,
a 7 kg weighing casting measuring 43 × 70 × 250 mm with a wall thickness of 48 mm
and with the composite zones present therein was produced. Then, two cross-sections
of the L450 steel casting were prepared by milling (Fig. 4b) and polishing (Fig. 4c).
In both cross-sectional areas are visible the composite zones fabricated
in situ from the casting inserts containing 50wt%, 60wt%, 70wt%, 80wt%, 90wt% and 97wt% of
the moderator addition in samples C3-C8, respectively, whereas composite zones containing
0wt%, 10wt% and 30wt% of the moderator addition in samples C1-C2, respectively, are
dispersed and invisible because of the total fragmentation effect taking place in
casting. The zone produced with 50wt% of the moderator addition has undergone partial
fragmentation, as proved by the presence of molten alloy penetrating into the zone
and splitting it into smaller fragments.
Table 4
Sample No. |
D1 |
D2 |
D3 |
D4 |
D5 |
D6 |
D7 |
D8 |
D9 |
Reactants of TiC formation [wt%] |
100 |
90 |
70 |
50 |
40 |
30 |
20 |
10 |
3 |
Moderator having the composition of Ni-Hard4 chromium cast iron containing Ni [wt%] |
0 |
10 |
30 |
50 |
60 |
70 |
80 |
90 |
97 |
The visibility of composite zones |
- |
- |
- |
+ |
+ |
+ |
+ |
+ |
+ |
Total fragmentation of composite zone |
+ |
+ |
+ |
- |
- |
- |
- |
- |
- |
Partial fragmentation of composite zone |
- |
- |
- |
+ |
- |
- |
- |
- |
- |
The content of macroporosity and fragments of composite zone in the upper part of
casting |
+ |
+ |
+ |
- |
- |
- |
- |
- |
- |
[0051] In the implementation of experimental studies, the casting wall thickness was set
in the range of 50 to 150 mm, which is a typical value for a number of cast structural
components used in the conical, jaw, hammer and impact crushers, and also for the
rolls or balls of ball or roller mills. In the aforementioned range of values, the
composite zones produced with the moderator content exceeding 60wt% were stable and
did not undergo fragmentation. For heavier casting walls, powder compositions with
higher content of the moderator can be used to reduce infiltration and produce stable
composite zones in such castings.
Example 2
[0052] In Example 2, casting inserts were fixed in the mould cavity to produce composite
zones reinforced with WC carbide as shown in Figure 5a. The casting inserts contained
the reactants of WC carbide formation and varying amounts of the powder moderator
having the composition of NiHard 4 white cast iron containing Ni. The composition
of the powder mixture used for the fabrication of casting inserts and the obtained
results are included in Table 5. The atomic ratio of the reactants to form WC carbide
was 94.93% W: 5.07% C. The moderator used for the manufacture of casting inserts E2-E9
contained the addition of a deoxidizer in the form of Al powder introduced in an amount
of 2wt%. The inserts were made by compaction under a pressure of 500 MPa and had dimensions
of 20 ×50 × X mm, where the value of dimension X depended on the compactability of
individual powder compositions. Compacts E1-E8 were made from samples of powder compositions
weighing 100 g each, whereas compact E9 was made from a sample weighing 150 g. Then,
polished cross-section was made (Fig. 5b) in a 7 kg weighing L450 steel casting measuring
43 × 70 × 250 mm and with a wall thickness of 48 mm. The polished cross-sectional
area shows the presence of composite zones formed
in situ from the casting inserts E1-E5, wherein said inserts have produced the dimensionally
stable zones reinforced with WC carbide, whereas zones E6-E9 have defects resulting
from the incomplete reaction taking place in compacts with a higher content of the
moderator. This points out to a different nature of the reaction of the SHS synthesis
of the formation of titanium carbide TiC and tungsten carbide WC. In the case of TiC,
high energy accompanying the reaction of synthesis and a relatively low activation
energy result in the fragmentation of the composite zone, and therefore preferably
the addition of moderator should be used in amounts exceeding 60wt%, whereas in the
case of WC carbide, said moderator should preferably be used in amounts not exceeding
60wt%, since higher content of this moderator tends to suppress the reaction and make
it inefficient. This causes defects in the area of the composite zone. The energy
associated with the reaction of the SHS synthesis and the activation energy are different
for TiC carbides and WC carbides, and therefore the formation of composite zones in
castings proceeds in a different way and depends on the type of the carbide used,
thus requiring different ranges of the content of moderator addition. In the composite
zones based on WC carbide, the phenomenon of fragmentation does not occur and these
zones can be produced with a low content of the moderator.
Table 5
Sample No. |
E1 |
E2 |
E3 |
E4 |
E5 |
E6 |
E7 |
E8 |
E9 |
Reactants of TiC formation [wt%] |
100 |
90 |
70 |
50 |
40 |
30 |
20 |
10 |
3 |
Moderator having the composition of Ni-Hard4 chromium cast iron containing Ni [wt%] |
0 |
10 |
30 |
50 |
60 |
70 |
80 |
90 |
97 |
The visibility of composite zones |
+ |
+ |
+ |
+ |
+ |
- |
- |
- |
- |
Total fragmentation of composite zone |
- |
- |
- |
- |
- |
- |
- |
- |
- |
Partial fragmentation of composite zone |
- |
- |
- |
- |
- |
- |
- |
- |
- |
The presence of macroporosity and absence of reaction |
- |
- |
- |
- |
- |
+ |
+ |
+ |
+ |
Example 3
[0053] In Example 3, casting inserts were fixed in the mould cavity to initiate the coupled
reaction of the SHS synthesis and produce the (Ti, W)C carbide as shown in Figure
6a. The casting inserts contained the TiC and WC reactants of the coupled SHS synthesis
of the (Ti, W)C carbide and varying amounts of the moderator in the form of a powder
mixture having the composition of NiHard4 white cast iron containing Ni. The composition
of the powder mixture used for the fabrication of casting inserts and the obtained
results are included in Table 6. The weight fraction of the reactants was 50% TiC
(where 55at% Ti : 45at% C) and 50wt% WC (where 94.93 at% W: 5.07 at% C). The moderator
used for the manufacture of casting inserts F1-F4 contained the addition of a deoxidizer
in the form of Al powder introduced in an amount of 5%, whereas in the case of inserts
F5-F8, the amount of the deoxidizer was reduced to 0.1%. The inserts were made by
compaction under a pressure of 500 MPa and had dimensions of 20 × 60 × X mm, where
the value of dimension X depended on the compactability of individual powder compositions.
Then polished cross-section was made (Fig. 5b) in a 7 kg weighing LGS30 steel casting
measuring 43 × 70 × 250 mm and with a wall thickness of 48 mm, said polished cross-section
being made on the top surface (Fig. 6b) of the casting and on the lateral surface
(Fig. 6c) of the casting. Both cross-sectional areas showed the presence of composite
zones formed
in situ from the casting inserts. The use of the coupled reaction of the SHS synthesis of
the TiC and WC carbides produced the dimensionally stable and fragmentation-resistant
composite zones reinforced with (Ti, W)C carbide with the moderator content of from
55 to 89.9wt%. Macroscopic observations revealed the presence of gas defects in zones
F6-F8 produced with a low content of the Al deoxidizer added in an amount of 0.1wt%,
whereas zones produced with the addition of 5wt% Al were free from the porosity defects.
Table 6
Sample No. |
F1 |
F2 |
F3 |
F4 |
F5 |
F6 |
F7 |
F8 |
Reactants of (Ti,W)C carbide formation [wt%] |
40 |
30 |
20 |
10 |
40 |
30 |
20 |
10 |
The amount of deoxidizer in the form of pure Al powder [wt%] |
5 |
5 |
5 |
5 |
0,1 |
0,1 |
0,1 |
0,1 |
Moderator having the composition of Ni-Hard4 chromium cast iron containing Ni [wt%] |
55 |
65 |
75 |
85 |
59, 9 |
69, 9 |
79, 9 |
89, 9 |
The visibility of composite zones |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
+ |
Total fragmentation of composite zone |
- |
- |
- |
- |
- |
- |
- |
- |
Partial fragmentation of composite zone |
- |
- |
- |
- |
- |
- |
- |
- |
The content of macroporosity and defects in the form of blowholes |
- |
- |
- |
- |
- |
+ |
+ |
+ |
[0054] For selected materials used in the fabrication of local composite zones according
to the present invention, microstructure was examined in a cross-section of the transition
region located between the composite zone and the remaining part of the steel casting
and also in a cross-section of the composite zone. Tests were performed on experimental
models included in Table 7.
Table 7
Sample No. |
D1 |
D2 |
D9 |
Matrix |
cast L35GSM steel |
cast L35GSM steel |
cast L450 steel |
Moderator type |
Cast high-manganese steel with 21wt% Mn |
Ni-Hard4 chromium cast iron |
Moderator content |
70wt% |
90wt% |
97wt % |
Results |
Fig. 5 |
Fig. 6 |
Fig. 7 |
Comments |
in each of Figures 7-9, photo (a) shows the cross-sectional view of transition region
between the composite zone and the matrix, whereas Figures 7-9 (b) - (d) or (b) -
(f) show magnified views of the composite zone |
Effects observed |
continuous phase boundary, absence of cracks and porosity, very good bond produced
by infiltration |
visible are submicron and nanometric particles of TiC |
visible are submicron and nanometric particles of TiC |
Table 8. Chemical composition of moderators used in the examples of embodiments
Composition of moderator |
Chemical composition [wt% ] |
C |
Mn |
Si |
Ni |
Cr |
Mo |
Fe |
Cast Hadfield high-manganese steel with 21% Mn |
1.2 |
21 |
0.5 |
- |
- |
- |
rest |
NiHard 4 chromium cast iron containing Ni |
3.6 |
0.8 |
2.2 |
5.5 |
10 |
0.5 |
rest |
High-chromium cast iron |
3.31 |
0.69 |
0.87 |
- |
26.6 |
1.25 |
rest |
[0055] Figures 7 and 8 show the images of microstructures of the composite zones produced
in cast L35GSM steel. The composite zones were made from the casting inserts containing
70wt% of moderator addition having the composition of cast Hadfield high-manganese
steel with 21wt% Mn, said moderator being a mixture of powders of Fe, FeMn, C, FeSi,
Al. The transition region between the composite zone and the rest of casting visible
in Figure 7a is characterized by a strong bond obtained in the controlled process
of infiltration and diffusion occurring in the liquid state between the area of the
in situ reaction zone and liquid alloy poured into the mould cavity. The phase boundary between
the composite zone and the rest of casting forms a straight line and is characterized
by continuity and dimensional stability. The fabricated composite zone contains mainly
the submicron-sized TiC carbides uniformly distributed within the area of the zone.
The visible effect of fragmentation enhances surface development of the TiC carbide
and its even distribution within the area of the zone, as observed in Figure 7 c-d.
Figure 8 shows that with a high content of the moderator added in an amount of 90wt%,
the distribution of the crystals of titanium carbide TiC in the composite zone is
less uniform, while clusters of the TiC crystals assume a specific shape of self-organizing
structures in the form of rings and chains visible in Figure 8f. The rings of these
chains are of a submicron and nanometric thickness.
[0056] The use of moderator in powdered form favourably affects the nucleation kinetics
and crystal growth in alloy melt during the reaction of the synthesis of carbides,
such as, for example, TiC, WC, (W, Ti) C, and other carbides undergoing the SHS reaction
that occurs between powder reactants of carbide formation contained in the powder
mixture, said powder mixture forming after compaction a casting insert. Particularly
preferred is the excellent dispersion of the crystals of, for example, TiC in a matrix
of the composite zone. It allows obtaining favourable operating parameters of the
composite zone at a relatively low percent content of carbides such as, for example,
titanium carbide TiC. The addition of moderator, introduced as a mixture of metal
and non-metal powders, significantly improves both hardness and wear resistance of
the composite zones obtained
in situ in castings.
[0057] Hardness testing was performed in local composite zones fabricated by the method
according to the present invention from materials of different compositions with different
content of the moderator according to the present invention. The results are shown
in Figures 10-13. Hardness of composite zones was tested in 7 kg weighing castings
measuring 43 × 70 × 250 mm with a wall thickness of 48mm, wherein said composite zones
were fabricated by the
in situ method.
[0058] The results of Vickers hardness measurements shown in Figures 11-14 were obtained
using samples of the size of 30 pieces each. Symbols used in the graphs denote: dot
- the average value; dash - the 50% median; frame - confidence limits for the deviation
2σ; x, x - extreme values. Hardness was measured under a load of 9,807 N (HV1) (a)
and 294,2N (HV30) (b).
[0059] In contrast to prior methods, the matrix of the composite zone according to the present
invention can be made from materials of the chemical composition characterized by
properties substantially different from the properties of the base casting alloy poured
into the mould cavity. This allows careful selection of the alloy providing the predictable
mechanical and functional properties, a repeatable process of synthesis and reproducible
distribution of the crystals of carbides such as, for example, titanium carbide TiC
in local composite zones.
[0060] The preferred features of the new method are confirmed by the results of comparative
hardness tests shown in Figures 11 and 12, wherein Figure 11 shows the relationship
between hardness of composite zones obtained
in situ in a casting made from the L450 steel and the amount of moderator in the form of
pure iron powder having properties close to the properties of the base casting alloy,
whereas Figure 12 shows the relationship between hardness of composite zones obtained
in situ in a casting made from the L35GSM steel and the amount of moderator, wherein the
applied reactants of the formation of titanium carbide TiC are mixed with moderator
powders, which by the reaction of the SHS synthesis form chromium cast iron having
properties substantially different from the properties of the base casting alloy.
[0061] The results of experimental studies indicate two important parameters influencing
the course of hardness changes. The first is the effect of moderator, which by stabilizing
the reactive infiltration process controls the dimensional stability of composite
zones. The dimensional stability ensures the maximum volume fraction of carbides in
the zone at a given content of the reactants of the formation of these carbides, and
hardness of the composite zone corresponding to this fraction. In addition to the
volume fraction of the obtained carbides, of some importance is also their morphology
and interconnections between the bridges formed. As can be seen in Figures 11-14,
the highest hardness is obtained in the zones reinforced with TiC carbide, when the
moderator content is 60÷70wt% of the powder composition used for the fabrication of
casting insert. This range of the moderator percent content in the composite zone
is optimal for moderators in the form of pure iron powders, a powder mixture having
the composition of chromium cast iron, a powder mixture having the composition of
cast Hadfield high-manganese steel with 21% Mn and a powder mixture having the composition
of Ni-Hard4 chromium cast iron containing Ni. The moderator having the composition
of Ni-Hard4 chromium cast iron (70wt%) was chosen as an optimal one to increase the
hardness of composite zones fabricated in a relatively soft cast L450 steel. The resulting
high value of hardness (1400HV1, Fig. 13) was due to a synergy between moderator powders
used in an amount of 70wt% to produce phases typical of Ni-Hard4 chromium cast iron
and reactants of the formation of titanium carbide TiC.
[0062] In a similar way, the moderator having the composition of cast manganese steel (Fig.
14) added in an amount of 70wt% produces high hardness values in the composite zone
(1200HV1) at a relatively low hardness of the base cast L450 steel (550HV1).
[0063] Optionally, the moderator composition may be supplemented with ceramic phases such
as aluminium oxide Al
2O
3 or zirconium oxide ZrO
2, including its stabilized varieties. The introduction of ceramic phases to the composite
zones can increase, through limited infiltration, the percent content of the reactants
of the formation of titanium carbide and thus significantly improve the resistance
to abrasion. The ceramic phases in the form of oxides introduced by themselves can
also increase the wear resistance of the composite zones and are less expensive than,
for example, titanium Ti used for the formation of TiC carbide. In this particular
case, the high percent content of the reactants of the formation of titanium carbide
TiC does not result in the composite zone fragmentation, since ceramic phases, especially
aluminium oxide, by having a high specific heat, absorb the heat formed during the
SHS synthesis, thus exerting control over the SHS process. The use of aluminium oxide
Al
2O
3 or zirconium oxide ZrO
2 in the moderator composition produces composite zones characterized by very high
resistance to abrasive wear, but practical use of such inserts is limited to those
applications where high impact resistance is not required.
[0064] In the composite zones reinforced with WC carbide, the highest hardness shown in
Figure 15 is obtained with a low content of the moderator. In this particular case,
however, hardness does not decrease with the increasing addition of the moderator.
As a consequence, preferably, using the addition of moderator, it is possible to produce
a reinforcement in the casting with a reduced amount of the expensive tungsten W.
Composite zones reinforced with the (Ti, W)C carbide, formed as a result of the coupled
reaction of synthesis, have preferable hardness values shown in Figure 16 at a 55%
level of the moderator addition.
[0065] In addition to the results of hardness measurements obtained for individual composite
zones and shown in Figures 11-14, Table 9 compares the results of abrasion resistance
testing carried out in selected composite zones. The measurements of the wear index
of the composite zones and of the cast L35GSM steel were taken by a Ball-on-Disc method
according to ISO 20808: 2004. The test results disclosed in the table below confirm
that the composite zones with high hardness are characterized by a low wear index.
For example, the composite zone based on a matrix made from the Ni-Hard4 chromium
cast iron has the hardness of 1400HV1 and, at the same time, the lowest wear index
of 7.07 * 10
-6 [mm
3/Nm].
Table 9
Description of composite zone |
Chemical composition of moderator |
Modera tor content |
Reactant s of TiC formatio n |
Disc wear index, W*10-6 |
|
wt % |
wt% |
wt% |
[mm3/N*m] |
Composite zone based on Ni-Hard4 chromium cast iron |
3.6-C; 2.2-Si; 0.8-Mn; 5.5-Ni; 10-Cr; 0.5-Mo; Fe - rest; |
70 |
30 |
7.07 |
Composite zone based on cast Hadfield steel |
12-Mn; 0.4-Si; 0.32-C; Fe- rest |
70 |
30 |
14.11 |
Composite zone based on cast Hadfield steel with the addition of Al2O3 and ZrO2-Y2O3
moderators |
70 % (12-Mn; 0.4-Si; 0.32-C; Fe- rest); 15 % (Al2O3 - 7.5; ZrO2-Y2O3 - 7.5) |
85 |
15 |
17.80 |
Composite zone based on high-chromium cast iron |
3.31-C; 0.87-Si; 0.69-Mn; 26.6-Cr; Fe rest |
70 |
30 |
21.95 |
Composite zone based on pure iron |
100-Fe |
70 |
30 |
137.23 |
Cast L35GSM steel |
- |
- |
- |
860 |
[0066] The method for producing local composite zones in castings according to the present
invention is illustrated in Figure 11 and described in Examples 4-7.
Example 4
[0067] Composite casting for use in an environment of high abrasive wear and low dynamic
loads. A mixture of titanium powders with the average diameter of less than 44.5 µm
and carbon powders with the average diameter of less than 3 µm was prepared, maintaining
the mutual atomic ratio of 1: 1. To 40wt% of the powder mixture of reactants of the
formation of titanium carbide TiC, the addition of 59wt% of a moderator was introduced,
said moderator being a powder mixture having the composition of Ni-Hard4 chromium
cast iron comprising Fe, Cr, Ni, Mn, Si, Mo and C, some of which were introduced in
the form of ferroalloys. Additionally, to the powder mixture, the addition of 1wt%
of a reducing component in the form of Al powder was introduced. Then all the powders
were mixed, dried and compressed under a pressure of 500 MPa. Thirty four casting
inserts of 10×20×100 mm dimensions were obtained, and said casting inserts were fixed
by means of assembly tools in the mould cavity in the area of the estimated highest
wear occurring in a 17 kg weighing casting. To remove moisture, mould with the fixed
set of casting inserts was dried with a gas burner. Said mould was next poured with
molten casting alloy having the composition of chromium cast iron. As a result, a
casting was obtained, reinforced with the composite zones containing mainly submicron
oval particles of the TiC carbide disposed in an austenitic matrix and containing
also particles of the Cr
7C
3 carbide.
Example 5
[0068] Composite casting for use in an environment of high abrasive wear and high dynamic
loads. A mixture of titanium powders with the average diameter of less than 44.5 µm
and carbon powders with the average diameter of less than 3 µm was prepared, maintaining
the mutual atomic ratio of 1: 1. To 30wt% of the powder mixture of reactants of the
formation of titanium carbide TiC, the addition of 69wt% of a moderator was introduced,
said moderator being a powder mixture having the composition of cast high-manganese
steel with 21wt% Mn comprising Fe, Mn, Si, C, some of which were introduced in the
form of ferroalloys, introducing also minor additions of other elements. Additionally,
to the powder mixture, the addition of 1wt% of a reducing component in the form of
Al powder was introduced. The reducing component was introduced in order to bind the
gases present in the compact. Then all the powders were mixed, dried and compressed
under a pressure of 500MPa. The obtained casting inserts of 15×20×100mm dimensions
produced in an amount of 100 pieces were placed in the area of the estimated highest
wear occurring in a 200 kg weighing casting. To remove moisture, mould with the fixed
set of casting inserts was dried with a gas burner. Said mould was next poured with
molten casting alloy having the composition of manganese steel containing 18wt% Mn.
As a result, a casting was obtained, reinforced with the composite zones containing
mainly submicron particles of the TiC carbide disposed in an austenitic matrix.
Example 6
[0069] Ultra-high abrasive wear resistant casting for use in an environment free from high
dynamic loads. A mixture of titanium powders with the average diameter of less than
44.5 µm and carbon powders with the average diameter of less than 3 µm was prepared,
maintaining the mutual atomic ratio of 1: 1. To 50wt% of the powder mixture of reactants
of the formation of TiC carbide, the addition of the following moderators was introduced:
10wt% of ZrO
2-Y
2O
3, 10wt% of Al
2O
3 and 29wt% of a powder mixture having the composition of cast high-manganese steel
containing 21wt% Mn. Additionally, to the powder mixture, the addition of 1wt% of
a reducing component in the form of Al powder was introduced in order to bind the
gases present in the compact. Then all the powders were mixed, dried and compressed
under a pressure of 500 MPa. As a result, casting inserts of 10 × 20 × 100 mm dimensions
were obtained and were next fixed by means of assembly tools in the mould cavity.
To remove moisture, mould with the fixed set of casting inserts was dried with a gas
burner. Said mould was next poured with molten casting alloy having the composition
of high-manganese steel containing 18wt% Mn. As a result, a 40 kg weighing casting
was obtained, reinforced with the zones comprising a hybrid composite of the TiC/Al
2O
3/ZrO
2-Y
2O
3/matrix type, consisting mainly of submicron and micron particles of the TiC carbide,
and of micron and millimeter particles of the Al
2O
3 and ZrO
2-Y
2O
3 oxides.
Example 7
[0070] Ultra-high abrasive wear resistant casting for use in an environment free from high
dynamic loads. A mixture of titanium powders with the average diameter of less than
44.5 µm and carbon powders with the average diameter of less than 3 µm was prepared,
maintaining the mutual atomic ratio of 1: 1. To 30wt% of the powder mixture of reactants
of the formation of titanium carbide TiC, the addition of 39wt% of a moderator was
introduced, said moderator being a powder mixture having the composition of cast high-manganese
steel containing 21% Mn, said mixture comprising Fe, Mn, Si, C, some of which were
introduced in the form of ferroalloys, introducing also minor additions of other elements
with the average diameter of less than 44.5 µm, and 30wt% of a ceramic moderator in
the form of Y
2O
3-stabilized ZrO
2 powder with the average diameter of less than 1 mm. Additionally, to the powder mixture,
1wt% of a reducing component in the form of Al powder was introduced. The reducing
component was introduced in order to bind the gases present in the compact. Then all
the powders were mixed, dried and compressed under a pressure of 500 MPa.
Example 8a
[0071] Casting inserts of 15 × 20 × 100 mm dimensions based on the powder mixture according
to Example 7 were produced and in an amount of 5 pieces were next fixed in a 7 kg
weighing casting in the area of the expected highest wear. To remove absorbed moisture,
mould with the set of casting inserts fixed inside was dried with a gas burner. Said
mould was next poured with molten casting alloy having the composition of L35GSM steel.
As a result, a casting was obtained, reinforced with the zones comprising a hybrid
composite of the TiC/ZrO
2-Y
2O
3/matrix type consisting mainly of submicron and micron particles of the TiC carbide,
and of micron and millimeter particles of the ZrO
2-Y
2O
3 oxide.
Example 8b
[0072] Casting insert in a first variant of the second embodiment. A mixture of titanium
powders with the average diameter of less than 44.5 µm and carbon powders with the
average diameter of less than 3 µm was prepared, maintaining the mutual atomic ratio
of 1: 1. To 45wt% of the powder mixture of reactants of the formation of titanium
carbide TiC, the addition of 10wt% of a moderator was introduced, said moderator being
a powder mixture having the composition of chromium cast iron comprising Fe, Cr, Mn,
Mo, Si, C, some of which were introduced in the form of ferroalloys, introducing also
minor additions of other elements with the average diameter of less than 44.5 µm,
and the addition of 45wt% of a ceramic moderator composed in 5wt% of the Y
2O
3-stabilized ZrO
2 powder with the average diameter of less than 100 µm and in 40wt% of the Al
2O
3 powder with the average diameter of less than 130 µm. Additionally, to the powder
mixture, 1wt% of a reducing component in the form of Al powder was introduced. Then
all the powders were mixed, dried and compressed under a pressure of 500 MPa to form
casting inserts of 15 × 20 × 100 mm dimensions.
Example 8c
[0073] Casting insert in a second variant of the second embodiment. A mixture of titanium
powders with the average diameter of less than 44.5 µm and carbon powders with the
average diameter of less than 3 µm was prepared, maintaining the mutual atomic ratio
of 1: 1. To 20wt% of the powder mixture of reactants of the formation of titanium
carbide TiC, the addition of 19wt% of a moderator was introduced, said moderator being
a powder mixture having the composition of chromium cast iron comprising Fe, Cr, Mn,
Si, C, some of which were introduced in the form of ferroalloys, and the addition
of 60wt% of a ceramic moderator composed of the Y
2O
3-stabilized ZrO
2 powder with the average diameter of less than 0.5 mm. Additionally, to the powder
mixture, 1wt% of a reducing component in the form of Al powder was introduced. Then
all the powders were mixed, dried and compressed under a pressure of 500MPa to produce
casting inserts of 15 × 20 × 100 mm dimensions.
[0074] Local composite zones are produced by placing casting inserts in the mould cavity,
said inserts being obtained by compacting a powder mixture comprising the reactants
of the formation of carbides undergoing the SHS synthesis, for example TiC carbides,
and a mixture of selected powders of metals and non-metals, which after casting solidification
form a composite matrix, said matrix being a casting iron-based alloy. The moderator
introduced in an amount of from 60 to 97wt% stabilizes the geometric dimensions of
the composite zones and prevents fragmentation of said zones in the course of reactive
infiltration that takes place during the synthesis of titanium carbide TiC in castings
with the wall thickness of from 10 to 150 mm. The minimum amount of the reactants
of the formation of titanium carbide TiC providing the
in situ formation of a composite matrix is 3wt%. Reducing the amount of the reactants of
the formation of titanium carbide TiC is not effective and does not lead to the formation
of designed structure of the composite matrix in the composite zone. The use of ceramic
structures based on aluminium oxide and zirconium oxide can increase the percent content
of TiC crystals (> 30%) in the composite zone, thereby producing a significant increase
in both hardness and abrasion resistance.
[0075] For the synthesis of composite zones reinforced with WC carbide, the moderator may
be used in amounts of up to 60wt%, as above this level the reaction is inefficient
and suppressed. Using the reactants of WC carbide formation with the addition of moderator
in an amount of up to 60wt% it is possible to obtain dimensionally stable composite
zones, as illustrated in Figure 5.
[0076] It is also possible to produce the composite zones according to the present invention
using mixtures of the reactants of the formation of, for example, TiC carbide and
WC carbide, as depicted in Figure 6. Then, as a result of the coupled reaction of
synthesis proceeding in the casting, carbides of the (W, Ti) C or (Ti, W)C type with
a core - ring structure are formed. Owing to the coupled reaction of synthesis, it
is possible to use a higher content of the moderator and control the mechanical properties
of the composite zone.
[0077] The powder compositions and casting inserts for the
in situ fabrication of composite zones in castings according to the present invention allow
an extensive use of different types of carbides and borides undergoing the reaction
of the SHS synthesis. Examples of the fabrication of composite zones in castings comprise
two extreme cases of the use of carbides and mixtures thereof; these are the TiC and
WC carbides, and a (W, Ti) C carbide, respectively.
1. A casting insert fabrication method using a composition of powders for the fabrication
of casting inserts designed to produce local composite zones resistant to abrasive
wear, wherein said composite zones reinforced with carbides and borides, or with mixtures
thereof, are formed in situ in castings, and wherein said composition of powders comprises:
powder reactants of the formation of carbides selected from the group of TiC, WC,
or mixtures thereof, wherein said carbides or borides after crystallization form particles
reinforcing the composite zones in castings, and moderator powders forming a mixture
of metal powders, wherein said metal powders after crystallization form matrix of
the composite zone in casting,
characterized in that
the amount of powder reactants for the formation of TiC carbide is from 3 to 40wt%
and the amount of moderator powders is from 60 to 97wt%,
the amount of powder reactants for the formation of WC carbide is from 40 to 99wt%
and the amount of moderator powders is from 1 to 60wt%, or
the amount of the mixture of powders for the reactants of the coupled reaction of
the synthesis of TiC and WC carbides is from 10 to 70wt% and the amount of moderator
powders is from 30 to 90wt%.
2. A casting insert fabrication method according to claim 1, characterized in that the powders of the reactants of the formation of carbides have particles of the size
of up to 100 µm, but preferably not larger than 45 µm.
3. A casting insert fabrication method according to claim 1, characterized in that carbon as a powder reactant is in the form of graphite, amorphous graphite, a carbonaceous
material or a mixture thereof, and in the case of Ti or, W these are the powders of
pure metals or alloys of said metals with other elements, or mixtures thereof.
4. A casting insert fabrication method according to claim 1, characterized in that the moderator powders additionally comprise a non-metal in the form of carbon.
5. A casting insert fabrication method according to claim 1 or 4, characterized in that the moderator powders from the group of metals comprise any powder selected from
the group of Fe, Co, Ni, Mo, Cr, W, Al, or comprise a mixture of said powders.
6. A casting insert fabrication method according to claim 5, characterized in that the moderator powders further comprise at least one powder selected from the group
of Mn, Si, Cu, B, or a mixture of said powders.
7. A casting insert fabrication method according to claim 1, characterized in that the moderator powders have the chemical composition of an alloy selected from the
group of grey cast iron, white cast iron, chromium cast iron, cast chromium steel,
cast unalloyed steel, cast low-alloy steel, cast Hadfield manganese steel, or Ni-Hard4
chromium cast iron containing Ni.
8. A casting insert fabrication method according to claim 1, characterized in that the moderator powder is a mixture of powders selected from the group of: (a) Fe,
Cr, Mn, Si, Mo, C; (b) Fe, Cr, Mn, Si, C; (c) Co, Cr, W, C; (d) Co, Fe, Ni, Mo, Cr,
C; (e) Ni, Cr, Mo, Nb, Al, Ti, Fe, Mn, Si; (f) Ni, Cr, Co, W, Nb, Al, Ti, C, B, Zr;
(g) Co, Ni, Fe.
9. A casting insert fabrication method according to claim 1, characterized in that the moderator powders also include phases of ceramic powders increasing the resistance
to wear, in particular the phases of ceramic powders selected from the group of ZrO2, stabilized ZrO2, Al2O3or a mixture thereof; and/or a reducing component in the form of Al and/or Si, wherein
the amount of the reducing component is maximum 5wt% of the powder composition.
10. A casting insert for the fabrication of local composite zones resistant to wear, comprising
reactants of the carbide formation, wherein said insert in the form of shapes, solids,
preforms or granules is characterized in that it is fabricated by a method according to any one of claims 1 to 9.
11. A method for the fabrication of local composite zones in castings, which uses the
reaction of self -propagating high-temperature synthesis (SHS), said method comprising
a preparation of a powder mixture, wherein said mixture comprises reactants of carbide
formation, and wherein said mixture is next compacted conferring to the compacted
powder composition a particular form, especially of shapes, solids, preforms or granules
forming a casting insert, and wherein at least one casting insert is next placed in
an interior of a mould, and said mould is poured with molten casting alloy in an amount
sufficient to initiate the SHS reaction, and wherein said method is further characterized in that the casting insert is fabricated by a method according to any one of claims 1 to
11.
12. The method according to claim 11, characterized in that after preparing the powder mixture, said mixture is dried, preferably at 200°C, until
the moisture content is maximum 2%.
13. The method according to claim 11, characterized in that the operation of compaction is performed under a pressure ranging from 450 MPa to
650 MPa.
14. The method according to claim 11, characterized in that the casting insert is placed in a mould cavity in a predetermined position and is
fixed to the mould with bolts or is placed on a steel frame, said frame being placed
inside the mould cavity, wherein preferably the steel frame consists of rods on which
compacts having holes are threaded.