TECHNICAL FIELD
[0001] The present invention relates to a composite material based on reinforced manganese
steel, a wear part made thereof and a method for making the same.
BACKGROUND
[0002] A particular category of wear resistant steels are typically referred to as manganese
steel or Hatfield steel. These materials are suitable for applications where a high
toughness and a moderate abrasion resistance are required including for example use
as wear parts for crushers that are subjected to strong abrasion and dynamic surface
pressures due to the rock crushing action. Abrasion results when the rock material
contacts the wear part and strips-off material from the wear part surface. Additionally,
the surface of the wear part is subjected to significantly high surface pressures
that cause wear part fatigue and breakage.
[0003] Manganese or Hadfield steel is typically characterised by having an amount of manganese,
usually above 11% by weight. However, the problem with manganese steel is that it
is typically too ductile for wear parts in modern crushers that are subject to extreme
operating conditions, meaning the at the lifetime of the wear parts is reduced and
the maintenance costs are increased. Therefore, the problem to be solved is to provide
a manganese steel with enhanced wear resistance.
[0004] A known solution is to reinforce at least part of the manganese steel with particles
having an increased hardness.
WO20200222662 discloses a composite material, however the problem with this material is that is
not provide an optimal balance between wear resistance and impact resistance and an
even more significant problem is that there is poor bonding between the reinforcing
particle and the manganese steel matrix and poor bonding between reinforced and non-reinforced
zones, which leads reduced wear resistance and premature failure of the wear parts.
[0005] Therefore, the problem to be solved to provide a composite material that can be used
for wear parts having an optimal balance between wear resistance and impact resistance,
wherein there is improved bonding between the reinforcing particles and the manganese
matrix and the bonding between the reinforced and non-reinforced zones in order to
reduce defects and cracking that would lead to premature failure of the wear parts.
DEFINITIONS
[0006] A "catalysis" is a metal powder or mixture of metal powders which during the reaction
in the self-propagating high temperature synthesis (SHS) undergo melting and form
a matrix of the composite zone. The fundamental role of catalysis is to reduce the
amount of dissipated energy in the SHS process.
[0007] A "compact" is a densified powder composition.
SUMMARY OF INVENTION
[0008] It is an objective of this invention to provide a novel and improved composite material
for wear parts. The objective is achieved by providing a composite material comprising:
at least one reinforcing zone comprising Niobium carbide (NbC) and a manganese steel
matrix; a manganese steel zone that surrounds each of the reinforcing zones; and an
interface layer positioned between each of the reinforcing zones and the manganese
steel zone; characterized in that: the average grain size of the NbC particles in
each of the reinforcing zone(s) is between 2-5 µm, preferably between 2-4 µm.
[0009] Advantageously, this produces a composite material that has both increased wear resistance
and structural integrity. Therefore, when the material is used on areas of wear parts
that are highly exposed to wear the lifetime of the parts is increased. If the average
grain size of the NbC grains is too large, then the composite material will be too
brittle. If the average grain size of the NbC grains in too small the wear resistance
will be reduced.
[0010] Preferably, the composite material comprises between 60-90 wt% of NbC in each of
the reinforcing zones. Preferably between 70-90 wt%, even more preferably between
80-90 wt%. Advantageously, this provides the optimal balance between wear resistance
and impact resistance. If the wt% of NbC in each of the reinforcing zones in too high
the composite material will be too brittle and more prone to failure. If the wt% of
the NbC in each of the reinforcing zones is too low, then composite material will
have low hardness and therefore it will not have sufficient wear resistance.
[0011] Preferably, the composition of the manganese steel in manganese steel zone has the
chemical composition by weight of: carbon: 0.5 to 2.0%; manganese: 11 to 22%; silicon:
0.2 to 1.0%; chromium: 1 to 2%; nickel: up to 0.6%; molybdenum: up to 0.5%; and a
balance of Iron. Advantageously, this steel composition is characterized by the addition
of micro-alloying elements such as chromium, nickel and molybdenum in good amounts
which induce high yield strength and high hardness resulting in increase in wear resistance
of manganese steel.
[0012] Preferably, the Vickers hardness of the reinforcing zones is between 600-1000 HV1
and the hardness of the manganese steel zone is between 200 - 300 HV1 before work
hardening. Advantageously, the increased hardness in the reinforcing zones leads to
a more wear resistant material.
[0013] Preferably, the thickness of each of the interface layer is between 90-300 µm, preferably
between 130-200, even more preferably between 250-300 µm. Advantageously, this thickness
of interface layer or thickness of contact area between manganese and composite zone
is an indication of an increase in the reaction propagation rate and the amount of
heat generated due to the high combustion temperature taking place at the contact
between the molten manganese steel and the insert. A high combustion temperature leads
to the precipitation of large grains at the interface. If the thickness is too large
the heat conductivity increases in the composite zone which results in a faster heat
dissipation towards the inside of the composite zone resulting in high nucleation
rate of NbC particles. If the thickness is too small the heat conductivity is less
which favours growth, consequently less nucleation of NbC particles.
[0014] Preferably, the interface layer is free of defects. Advantageously, the absence of
any defects in the interface layer means that there is good bonding between the manganese
steel zone and each of the reinforcing zones and consequently the structural integrity
of the composite material is improved, meaning that the lifetime of the wear parts
that the materials is used in is increased. Further, the absence of the presence of
any pores is an indication that the composition has the ability to absorb the excess
heat and gases from the SHS process and so therefore signifies that the synthesis
reaction has been successful.
[0015] Preferably, the wettability between the NbC grains and the manganese steel in the
reinforcing zone (s ) is >99%, preferably >99.5%, even more preferably >99.9%. Advantageously,
good wettability induces an excellent bonding between the composite zone and manganese
steel preventing defects such as pores and cracks to form and consequently the wear
resistance increases.
[0016] Preferably, the each of the reinforcing zones has a volume of between 30-75 cm
3. Advantageously, this size provides the optimal balance between wear resistance and
impact resistance.
[0017] Preferably, at least 90% of the NbC grains in the reinforcing zones have a square
prismatic shape. Advantageously, the square prismatic shape of NbC will contribute
to crack deflection and stop crack propagation increasing the ductility and high wear
resistance of the reinforcing zone.
[0018] Preferably, the distance between two neighbouring reinforcing zones is between 1-5
mm, preferably between 1-3 mm, more preferably between 1-2 mm. Advantageously, this
provides the optimal balance between wear resistance and impact resistance. If the
reinforcing zones are spaced too far apart then the wear resistance will not be high
enough. If the reinforcing zones are spaced to close together then the impact resistance
will not be high enough.
[0019] Another aspect of the present invention relates to a wear part comprising the composite
material as described hereinbefore or hereinafter. Advantageously, the presence of
the reinforcing zones within the manganese zone will improve the wear resistance and
therefore the lifetime of the wear parts which in turn increases profitability.
[0020] Another aspect of the present invention relates to a method of producing the composite
material as described hereinbefore or hereinafter comprising the steps of: a) mixing
together 50-90 wt% niobium, 6-20t% carbon and 0-40 % catalysis powders; b) compacting
the mixed powders together to form at least one compact; c) positioning and optionally
fixing at least one compact into the interior of a mold; d) pouring molten casting
manganese steel into the mold to surround the at least one compact to initiate a self-propagating
high temperature synthesis (SHS) reaction to produce a cast; e) heat treating the
cast; f) quenching the cast; characterized in that: in step b) the powders are compacting
with a pressure of between 450-700 MPa, preferably between 500-650 MPa, more preferably
between 550-650 MPa.
[0021] Advantageously, if this pressing pressure is used the compacts have a low density
which enables the manganese steel to more easily infiltrate between the NbC grains
and consequently results in improved bonding between the NbC grains and the manganese
steel. Further it avoids the creation of defects which would lead to premature failure
of the wear parts that the composite material is used in.
[0022] Preferably, the catalysis is selected from Fe, Mn, Ni, Mo, Cr, W, Al, or a mixture
thereof. Advantageously, he addition of a catalysis in a specific amount will contribute
to a strong stabilization to austenite phase within the microstructure in addition
to good mechanical properties and high wear resistance. The catalysis addition will
also act as a grain growth inhibitor which results in a fine microstructure.
BRIEF DECRSIPTION OF DRAWINGS
[0023]
Figure 1: Shows a line drawing of the composition of the composite material.
Figure 2: Shows an SEM image taken of the reinforced zone with low magnification on
the left and high magnification on the right.
Figure 3: Shows an SEM image taken of the interface layer with low magnification on
the left and high magnification on the right.
Figure 4: Shows an SEM image of the composite material.
Figure 5: Shows a perspective drawing of a wear part.
Figure 6: Shows an SEM image of a comparative sample having pores in the interface
layer (left picture) and reinforced zone (right picture).
DETAILED DESCRIPTION
[0024] Figure 1 shows a composite material 2 comprising at least one reinforcing zone 4
comprising niobium carbide (NbC) and a manganese steel matrix; a manganese steel zone
6 that surrounds each of the reinforcing zones 4 ; and an interface layer 8 positioned
between each of the reinforcing zones 4 and the manganese steel zone 6. In each of
the reinforcing zones, the NbC acts to reinforce the manganese steel matrix.
[0025] The average grain size of the NbC particles in each of the reinforcing zone(s) (4)
is between 2-5 µm, preferably between 2-4 µm, most preferably between 2-3µm.
[0026] The average grain size of the NbC grains is measured by Scanning Electron Microscopy
(SEM) analysis where several and different areas from the samples were analysed and
particle sizes were measured. Then, the average particle size was calculated.
[0027] Each interface layer 8 comprises NbC and manganese steel and can be distinguished
from the reinforcing zones 4 as the shape and size of the NbC grains are different.
The interface layer(s) 8 can be distinguished from the reinforcing zone(s) 4 can either:
comparing the geometry and / or comparing the average grain size. If the geometry
is being compared, the reinforcing zone(s) 4 comprise >90% NbC grains having a square
prismatic geometry whereas the interface layer(s) 8 comprise <5% NbC grains having
a square prismatic geometry. A NbC grain is considered to have square prismatic geometry
if the grains have 4 sharp edges. If the grain size is being compared the average
NbC grain size of in the interface layer(s) 8 is at least 5% less than the average
NbC grain size on the reinforcing zone(s) 4.
[0028] Figure 2 shows a Scanning Electron microscope image using MIRA3 TESCAN equipment.
A secondary electron detector (SE) with a high voltage of 15 KV and a working distance
of 9 mm configuration were used. SEM image of the NbC grains in the reinforcing zone
4. Figure 3 shows an SEM image of the NbC grains in the interface layer 8. The different
NbC grain geometry and size can be clearly be seen when comparing these two figures.
[0029] In one embodiment the wt% of NbC in each of the reinforcing zones 4 is between 60-90
%, more preferably between 80-91 %, even more preferably between 80-90%.
[0030] In one embodiment, the composition of the manganese steel in manganese steel zone
6 has the chemical composition by weight of: carbon: 0.5 to 2.0%; manganese: 11 to
22%; silicon: 0.2 to 1.0% ; chromium: 1 to 2%; nickel: up to 0.6%, molybdenum: up
to 0.5% and a balance of Fe.
[0031] In one embodiment, the chemical composition of the manganese steel in each of the
reinforcing zones 4 has the chemical composition by weight of: 1-1.5 % C, 11-14 %
Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % P.
[0032] In one embodiment, the hardness of the reinforcing zones 4 is between 600-1000HV1,
preferably between 750-1000. The hardness of the manganese steel zone 6 is between
200 - 300 HV1.
[0033] Hardness is measured using Vickers hardness mapping on polished samples using a 1
kg. and a holding time of 15 seconds. A micro-hardness tester, Matsuzawa, model MXT
was used. Hardness measurement profiles are performed starting from the non-reinforce
zone, moving to the interface layer and then to the reinforced zone.
[0034] In one embodiment, the interface layer 6 is between 90-300 µm wide, preferably between
130-200. Figure 4 shows an SEM image taken at 15.0 kV, 563 magnification of the reinforced
zone 4, the manganese steel zone 6 and the interface layer 8. The width of the interface
layer 6 is measured from a start point 10, which is defined as being adjacent to the
manganese steel zone 6 and the point at where the NbC grains are present. The end
point 12 for measuring where the interface layer 8 ends, and therefore where the reinforcing
zone 8 starts is considered to be where the average grain size of the NbC grains has
increased by 20% compared average NbC grains measured at the start point 10 and /
or where the percentage of NbC grains having a square prismatic shape increases above
90%.
[0035] In one embodiment, the interface layer 8 is free of defects. Defects are considered
to be cracks or pores.
[0036] In one embodiment, the wettability between the NbC grains and the manganese steel
in the reinforcing zones 4 is >99%, preferably >99.5%, more preferably >99.9%, most
preferably 100%. Wettability is measured by a Scanning Electron Microscope where the
contact area and the bonding between the NbC grains and the manganese steel have been
evaluated.
[0037] In one embodiment each of the reinforcing zones 4 has a volume of between 30-75 cm
3. For example, but not limited to the reinforcing zone(s) 4 could have a length of
between 100-200 mm, preferably between 100-150 mm, a width of between 20-30 mm, preferably
between 20-25 mm and a thickness between 15-30 mm, preferably between 15-25 mm.
[0038] In one embodiment >95%, preferably >98%, more preferably >99% of the NbC grains in
the reinforcing zones 4 have a square prismatic shape. Preferably, the NbC grains
are uniformly distributed in the manganese steel in the reinforcing zone(s).
[0039] In one embodiment, there are a plurality of reinforcing zones 4 with its interface
zone 8 and the distance between two neighbouring reinforcing zones 4 with its interface
layer 8 is between 1-5 mm, preferably between 1-3 mm, more preferably between 1-2
mm.
[0040] Figure 5 shows an example of a wear part 14 comprising the composite material 2 as
described hereinabove or hereinafter. For example, the wear part 2 could be, but not
limited to, a cone crusher or a stationary jaw crusher or a mobile jaw crusher that
is configured to crush material or other material/rock processing unit. The reinforcing
zone(s) 4 are positions on the wear parts 14 in the locations that are most subjected
to high wear, for example on a crushing zone 18 of a cone crusher 16.
[0041] The method for producing the composite material 2 as described hereinbefore or hereinafter
comprising the steps of: a) Mixing together 50-90 wt%, preferably 77-90 niobium; 6-20
wt%, preferably 10-20 wt% carbon and 0-40 wt%, preferably 0-10 wt% catalysis powders;
b) compacting the mixed powders together to form at least one compact using a compacting
pressure of between 450-700 MPa, preferably 500-650 MPa more preferably 550-650 MPa
; c) positioning and optionally fixing at least one compact into the interior of a
mold; d) pouring molten casting manganese steel into the mold to surround the at least
one compact to initiate a self-propagating high temperature synthesis (SHS) reaction
to produce a cast; e) heat treating the cast; and then f) quenching the cast.
[0042] Preferably, the cast is treated at a temperature of between 1400-1500°C, the cast
is quenched using water. Preferably, the catalysis is selected from Fe, Co, Ni, Mo,
Cr, W, Al, or a mixture thereof. Carbon could be added in the form of graphite, amorphous
graphite, a carbonaceous material or mixtures thereof. The compacts could for example
be held in place using me a metallic fixation system to hold them in place during
casting.
EXAMPLES
Example 1 - Samples
[0043] Sample A is a comparative sample of non-reinforced manganese steel having the composition
1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % P.
[0044] Samples B-H are samples of composite materials produced by mixing together powders
of niobium, carbon and a catalysis powder. The compacting the mixed powders to form
compacts which were then positioned in a mold and then molten manganese steel having
a composition of 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065
% was poured into the mold to surround the compacts which initiated a SHS reaction,
the cast was then heat treated at a temperature of 1450 °C and then quenching with
water. Table 1 shows a summary of the reinforced samples:
Table 1: Summary of samples
Sample |
Compacting pressure used (MPa) |
Average NbC grain size in reinforced zone (µm) |
NbC content in reinforced zone (wt%) |
Wettability (%) |
A (comparative) |
- |
- |
- |
- |
B (inventive) |
620 |
2 |
90 |
100 |
C (inventive) |
600 |
2 |
85 |
100 |
D (inventive) |
600 |
2 |
80 |
100 |
E (inventive) |
650 |
2.5 |
90 |
100 |
F (comparative) |
550 |
1 |
50 |
5 |
G (inventive) |
600 |
2 |
87 |
100 |
H (inventive) |
600 |
3 |
70 |
100 |
[0045] It can be seen if the compacting pressure is not high enough then the wettability
is reduced.
Example 2 - Hardness
[0046] Vickers hardness was measured by a micro-hardness tester, Matsuzawa, model MXT using
1 kgf and a holding time of 15 seconds. Hardness measurement profiles are performed
starting from the non-reinforce zone, moving to the interface layer and then to the
reinforced zone.
[0047] The hardness measurement results are shown in Table 2 below:
Table 2: Hardness measurement
Sample |
Hardness in manganese steel zone (HV1) |
Hardness in Interface layer |
Hardness in reinforced zone |
A (comparative) |
300 |
- |
- |
B (inventive) |
254 |
614 |
757 |
C (inventive) |
249 |
663 |
738 |
D (inventive) |
257 |
596 |
724 |
E (inventive) |
238 |
673 |
820 |
F (comparative) |
270 |
630 |
670 |
G (inventive) |
300 |
643 |
834 |
H (inventive) |
250 |
655 |
963 |
[0048] It can be seen that the inventive samples have an increased hardness in reinforced
zones compared to the comparative samples.
Example 3 - Wear test
[0049] Wear was tested using a standard wear test using a lab jaw crusher. The wear test
procedure consists on using fixed amount of rocks from 1 Ton up to 4 Ton of rocks.
Four plates, two stationary and two moving, were placed inside the jaw crusher. Reference
plates were also mounted in both positions. The reference plates are based on Weldox
type of material.
[0050] The calculation of wear is based on the difference in volume loss of the test plates
compared to the reference plates. All plates were weighed before and after wear test.
Then volume loss is calculated using the density of 7.85 g/cm
3 and 7.6 g/cm
3 for the reference and test plates respectively. The total wear ratio (WR) is calculated
according to ASTM G81-97a(2013).
[0051] The wear test results are shown in table 3 below:
Table 3: Wear test results
Sample |
Wear ratio rate |
E |
0.23 |
B |
0.24 |
[0052] It can be seen that the wear rate for the inventive samples is low.
Example 4 - Defects
[0053]
Table 4: Defects
Sample |
Defects in the reinforced zone |
Defects in the interface layer |
A (comparative) |
- |
|
B (inventive) |
none |
none |
C (inventive) |
none |
none |
D (inventive) |
none |
none |
E (inventive) |
none |
none |
F (comparative) |
pores |
pores |
G (inventive) |
none |
none |
H (inventive) |
none |
none |
[0054] Defects were assessed by using Scanning Electron microscopy analysis where cracks
and pores are identified. It can be seen that the inventive samples are free of defects.
It can be seen that the comparative sample contains pores, whereas the inventive samples
do not. Figure 6 shows the pores in sample F, whereas figure 4 shows the absence of
any pores from sample B.
1. A composite material (2) comprising:
at least one reinforcing zone (4) comprising niobium carbide (NbC) and a manganese
steel matrix;
a manganese steel zone (6) that surrounds each of the reinforcing zones (4); and
an interface layer (8) positioned between each of the reinforcing zones (4) and the
manganese steel zone (6);
characterized in that:
the average grain size of the NbC particles in each of the reinforcing zone(s) (4)
is between 2-5 µm.
2. The composite material (2) according to claim 1 wherein the wt% of NbC in each of
the reinforcing zones (4) is between 60-98.
3. The composite material (2) according to claim 1 or claim 2 wherein the composition
of the manganese steel in manganese steel zone (6) has the chemical composition by
weight of:
carbon: 0.5 to 2.0%;
manganese: 11 to 22%;
silicon: 0.2 to 1.0% ;
chromium: 1 to 2%;
nickel: up to 0.6%
molybdenum: up to 0.5%
and a balance of iron.
4. The composite material (2) according to any of the previous claims wherein the hardness
of the reinforcing zones (4) is between 600-1000 HV1 and the hardness of the manganese
steel zone (6) is between 200 - 300 HV1 before work hardening.
5. The composite material (2) according to any of the previous claims wherein the thickness
of each of the interface layer (6) is between 90-295 µm.
6. The composite material (2) according to any of the previous claims wherein the interface
layer 8 is free of defects.
7. The composite material (2) according to any of the previous claims wherein wettability
between the NbC grains and the manganese steel in the reinforcing zones (4) is >99%.
8. The composite material (2) according to any of the previous claims wherein each of
the reinforcing zones has a volume of between 30-75 cm3.
9. The composite material (2) according to any of the previous claims wherein at least
90% of the NbC grains in the reinforcing zones (4) have a square prismatic shape.
10. The composite material (2) according to any of the previous claims wherein there are
a plurality of reinforcing zones (4) and the distance between two neighbouring reinforcing
zones is between 1-5 mm.
11. A wear part (14) comprising the composite material (2) according to any of claims
1-10.
12. A method of producing the composite material (2) according to any of claims 1-10 comprising
the steps of:
a) mixing together 50-90 wt% niobium, 6-20 wt% carbon and 0-40 wt% catalysis powders;
b) compacting the mixed powders together to form at least one compacts (20);
c) positioning and optionally fixing at least one compact (20) into the interior of
a mold (22);
d) pouring molten casting manganese steel (24) into the mold (22) to surround the
at least one compact (20) to initiate a self-propagating high temperature synthesis
(SHS) reaction to produce a cast (26);
e) heat treating the cast (26)
f) quenching the cast (26)
characterized in that:
in step b) the powders are compacting with a pressure of between 450-700 MPa.
13. The method according to claim 12 wherein the catalysis is selected from iron, cobalt,
nickel, molybdenum, chromium, tungsten, aluminum, or a mixture thereof.