AU2019380489B2 - Binder redistribution within a cemented carbide mining insert - Google Patents
Binder redistribution within a cemented carbide mining insert Download PDFInfo
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- AU2019380489B2 AU2019380489B2 AU2019380489A AU2019380489A AU2019380489B2 AU 2019380489 B2 AU2019380489 B2 AU 2019380489B2 AU 2019380489 A AU2019380489 A AU 2019380489A AU 2019380489 A AU2019380489 A AU 2019380489A AU 2019380489 B2 AU2019380489 B2 AU 2019380489B2
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/24—After-treatment of workpieces or articles
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/08—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F5/00—Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product
- B22F2005/001—Cutting tools, earth boring or grinding tool other than table ware
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2207/00—Aspects of the compositions, gradients
- B22F2207/01—Composition gradients
- B22F2207/03—Composition gradients of the metallic binder phase in cermets
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B10/00—Drill bits
- E21B10/46—Drill bits characterised by wear resisting parts, e.g. diamond inserts
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Powder Metallurgy (AREA)
- Earth Drilling (AREA)
- Cutting Tools, Boring Holders, And Turrets (AREA)
Abstract
A method of redistributing the binder phase of a cemented carbide mining insert comprising one or more hard-phase components and a binder comprising the steps of: a) providing a green cemented carbide mining insert; b) applying at least one binder puller selected from a metal oxide or a metal carbonate to the surface of the green cemented carbide mining insert; and c) sintering the green cemented carbide mining insert characterized in that the metal oxide or metal carbonate is only applied to at least one local area on the surface of the green cemented carbide mining insert, also a cemented carbide having a hardness gradient and the use thereof.
Description
The present disclosure relates to a method of redistributing the binder within a cemented
carbide mining insert, a cemented carbide mining insert with a hardness gradient and the use
thereof.
The discussion of the background to the invention that follows is intended to facilitate an understanding of the invention. However, it should be appreciated that the discussion is not an acknowledgement or admission that any aspect of the discussion was part of the common general
knowledge as at the priority date of the application.
Cemented carbide has a unique combination of high elastic modulus, high hardness, high
compressive strength, high wear and abrasion resistance with a good level of toughness. Therefore,
cemented carbide is commonly used in products such as mining tools. In general, the hardness and
toughness of cemented carbide can be altered by changing the binder content and grain size of the hard phase. Typically, a higher binder content will increase the toughness of the cemented carbide but will decrease its hardness and wear resistance. A finer hard phase grain size will result in cemented carbide with a higher hardness which is more wear resistant, whereas a coarser hard
phase grain size will not be as hard but will have higher impact resistance.
For maximised efficiency of cemented carbides mining inserts, a combination of these
properties is desired and there are different demands on the material in different parts of the
product. For example, in inserts for rock drilling and mineral cutting, it is desirable to have a tougher interior to minimize the risk of failure and a harder exterior to optimise wear resistance.
WO 2010/056191 discloses a method of forming a cemented carbide body comprising a
hard phase and a binder phase, wherein at least one part of the intermediate surface zone has
lower average binder content than a part further into the body.
There is however still a need for a method which is able to create even greater hardness gradients, able to tailor the gradient to a specific application and which could be applied even to
non-symmetrical cemented carbide mining inserts. There is also a need to for a method which can
redistribute the binder phase starting with a standard carbide powder which is stoichiometrically
balanced with respect to carbon content.
Thus, the present disclosure therefore provides a method of redistributing the binder phase of a cemented carbide mining insert comprising a WC hard-phase component, optionally one or
more further hard-phase components and a binder comprising the steps of: a) providing a green cemented carbide mining insert; b) applying at least one binder puller selected from a metal oxide or a metal carbonate to the surface of the green cemented carbide mining insert; and c) sintering the green cemented carbide mining insert; wherein the metal oxide or metal carbonate is applied
to a local area on the surface of the green cemented carbide at the top of mining insert in the form
of a liquid dispersion or a slurry; and wherein post sintering the cemented carbide mining insert is
treated with a "High Energy Tumbling" process, wherein post tumbling a homogenous cemented
carbide mining insert has been deformation hardened such that AHV3% 9.72 - 0.00543*HV3bulk.
This method allows the binder to be re-distributed in a tailored and most favourable manner to provide optimal functionality to the cemented carbide mining insert. For examples,
specific hardness profiles can be created for different application.
Additionally, the present disclosure relates to a cemented carbide mining insert comprising
one or more hard-phase components and a binder wherein there is a hardness gradient from a first
part of the surface to a second part of the surface of the cemented carbide mining insert, wherein the first part of the surface is substantially opposing the second part of the surface, such that post sintering: - the first part of the surface is between 30HV3 softer and 80HV3 harder than the second
part of the surface; and - the first part of the surface is between 5 and 120 HV3 harder than the
bulk; and - the second part of the surface is between 20HV3 and 70HV3 harder than the bulk; and
wherein there is a minimum concentration (%binder-min) within the cemented carbide mining
insert at a depth, in percentage of the total height of the sintered cemented carbide mining insert,
of between 0.5-10 mm from the first part of the surface.
Where any or all of the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification (including the claims) they are to be interpreted as specifying the presence of the stated features, integers, steps or components, but not precluding the presence of one or more other features, integers, steps or components.
Figure 1: Schematic drawing of an insert showing the binder puller and binder pusher applied
symmetrically to opposing sides.Figure 2: Schematic drawing of an insert showing the binder puller
and binder pusher applied asymmetrically to opposing sides.
Figure 3: HV3 iso-hardness plots for sample A disclosed in example 1.
Figure 4: HV3 iso-hardness plots for sample B disclosed in example 1.
Figure 5: HV3 iso-hardness plots for sample C disclosed in example 1.
Figure 6: HV3 iso-hardness plots for sample D disclosed in example 1.
Figure 7: HV3 iso-hardness plots for sample E disclosed in example 1.
Figure 8: HV3 iso-hardness plots for sample F disclosed in example 1.
Figure 9: HV3 iso-hardness plots for sample G disclosed in example 1.
Figure 10: HV3 iso-hardness plots for sample H disclosed in example 1.
Figure 11: HV3 iso-hardness plots for sample I disclosed in example 1.
Figure 12: HV3 iso-hardness plots for sample J disclosed in example 1.
Figure 13: HV3 iso-hardness plots for sample K disclosed in example 1.
Figure 14: Schematic drawing of an insert showing where the binder puller was applied in example 1.
Figure 15: HV3 centre line hardness profiles for samples A, B and C disclosed in example 1.
Figure 16: HV3 centre line hardness profiles for samples D, E and F disclosed in example 1.
Figure 17: HV3 centre line hardness profiles for samples G, H and I disclosed in example 1.
Figure 18: HV3 centre line hardness profiles for samples J and K disclosed in example 1.
Figure 19: HV5 iso-hardness plots for example 2 wherein the binder puller and binder pusher are applied asymmetrically.
Figure 20: Schematic drawing of the set up for the pendulum hammer test.
Figure 21: Cobalt concentration profiles as discussed in example 5 for samples D and G.
Figure 22: Chromium concentration profiles as discussed in example 5 for samples D and G.
Figure 23: Cr/Co concentration profiles as discussed in example 5 for samples D and G.
Figure 24: Cobalt concentration profiles as discussed in example 5 for sample K.
Figure 25: Chromium concentration profiles as discussed in example 5 for sample K.
Figure 26: Plot showing change in insert diameter as a function of drilling depth for samples C, F and I measured during a field trial.DETAILED DESCRIPTION
According to one aspect, the present disclosure relates to a method of redistributing the
binder phase of a cemented carbide mining insert comprising a WC hard-phase, optionally one or
more further hard-phase components and a binder comprising the steps of:
a) providing a green cemented carbide mining insert;
b) applying at least one binder puller selected from a metal oxide or a metal carbonate to
the surface of the green cemented carbide mining insert; and
c) sintering the green cemented carbide mining insert;
characterized in that the metal oxide or metal carbonate is only applied to at least one local area on
the surface of the green cemented carbide mining insert.
The one or more further hard-phase components may be selected from TaC, TiC, TiN, TiCN,
NbC, CrC. The binder phase may be selected from Co, Ni, Fe or a mixture thereof, preferably Co and/
or Ni, most preferable Co. The carbide mining insert has a suitable binder content of from about 4 to
about 30 wt%, preferably from about 5 to about 15 wt%. The carbide mining insert may optionally
also comprise a grain refiner compound in an amount of 20 wt% of the binder content. The grain
refiner compound is suitably selected from the group of carbides, mixed carbides, carbonitrides or nitrides of vanadium, chromium, tantalum and niobium. With the remainder of the carbide mining
insert being made up of the one or more hard-phase components.
In one embodiment of the method, the cemented carbide mining insert contains a hard
phase comprising at least 80 wt% WC, preferably at least 90 wt%.
In the present disclosure, the term "green" refers to a cemented carbide mining insert
produced by milling the hard phase component(s) and the binder together and then pressing the
milled powder to form a compact cemented carbide mining insert, which has not yet been sintered.
The term "binder puller" refers to a substance which when applied to the surface of the cemented
carbide mining insert will cause the binder to migrate towards that surface during the sintering step,
i.e. the binder is pulled in the direction towards the surface where the "binder puller" has been
applied. The binder puller works by locally consuming carbon which causes the binder to flow from
the areas having normal carbon levels to the local area where the carbon level has been depleted.
The inventors have found that applying the binder puller, which is selected from a metal
oxide or a metal carbonate, to the surface of the green cemented carbide mining insert in at least
one local area, that carbon is locally consumed in this area during sintering which causes the having normal or higher levels of carbon to the local area which has a depleted carbon level. This will therefore form a binder rich region on a local area of the surface of the cemented carbide mining insert. The surface of the green cemented carbide mining insert where the binder puller is applied is referred to as the "oxide / carbonate doped" surface. It is well known that binder rich regions and binder depleted regions will be in tensile stress and compressive stress respectively after sintering. It would normally not be favourable to introduce tensile stresses. However, the inventors have found that after a treatment, such as centrifugal tumbling, high levels of compressive stress, down to at least 1mm depth below tumbled surface, can be introduced to counteract the tensile stresses present. Therefore, the benefit of applying the binder puller can be gained without the detrimental effect of introducing tensile stresses.
The "at least one local area on the surface of the green cemented carbide mining insert"
could be at any position on the surface, for example the tip, the base or the side depending on
where the requirement to create an increase in binder content is. The binder puller may be applied
to one or more local areas on the surface of the cemented carbide mining insert depending on
whether the desired effect is to create a local increase in toughness or wear resistance. Each "local
area" may be 0.5-85% of the total surface area of the cemented carbide mining insert, preferably 3
75%.
The sintering temperature is suitably from about 1000°C to about 1700°C, preferably from
about 1200°C to about 1600°C, most preferably from about 1300°C to about 1550°C. The sintering
time is suitably from about 15 minutes to about 5 hours, preferably from about 30 minutes to about
2 hours.
In one embodiment of the method, the binder puller, being a metal oxide or metal
carbonate is selected from Cr 20 3 , MnO, MnO 2 , MoO 2, Fe-oxides, NiO, Nb 2 , V 02 3 , MnCO 3, FeCO 3 ,
CoCO 3, NiCO 3, CuCO 3 or Ag 2 CO 3 . It would also be possible to alternatively apply a metal to the
surface of the green cemented carbide mining insert which upon heating, during the sintering step,
would form an oxide. The selection of the metal oxide or metal carbonate will influence the
properties of the cemented carbide post sintering e.g. deformation hardening, heat resistance and/
or corrosion resistance and the selection can be made to be best suited to the required application.
Metal carbonates would be selected if the equivalent metal oxide is toxic and the metal carbonate is
not. In this method, there is a high degree of freedom as to where the binder puller is applied, for
example it could be applied in or away from the wear zones of the carbide tool, depending on
whether the metal in the oxide or carbonate improves the wear resistance of the cemented carbide
or not.
In one embodiment of the method, the binder puller is Cr 20 3. Using Cr 203 as the binder
puller has the advantage that a chromium alloy rich surface layer will form, which has an enhanced
response to a tumbling treatment. Therefore, higher compressive stresses will be introduced, and
the wear properties of the cemented carbide mining insert will be improved. The Cr 3 02 contributes
towards grain refinement and hence, a reduced grain size is measured on the side of the insert
where the Cr 302 has been applied.
The metal oxide or metal carbonate is suitably provided onto the surface or surfaces in an
amount of from about 0.1 to about 100mg/cm 2, preferably in an amount of from about 1 to about
50 mg/cm 2. The starting cemented carbide powder blend should suitably have a carbon balance
equivalent to 0.95<Com/%Co<1 or have an excess of carbon that would compensate for the carbon
reduction from the application of the oxide or carbonate. Com is 100*SInsert/ S, Cobalt wherein as is
the weight specific saturation magnetization measured in Tm 3/kg and s, Cobalt = 2.01E-4 Tm 3/kg. Com
is measured in a Foerster Koerzimat CS.1097 unit.
In one embodiment of the method, the binder puller is applied to the top of the cemented
carbide mining insert. In another embodiment of the method, the binder puller is applied to the side of the cemented carbide mining insert. Therefore, the properties of the cemented carbide mining
insert can be tailored to be suited to the application. The binder puller is likely chosen to be applied
to the position on the surface of the cemented carbide mining insert that is exposed to the highest
wear.
In one embodiment, the method further comprises the step between steps a) and b) of
applying at least one binder pusher to at least one different local area on the surface of the green
cemented carbide mining insert. In the present disclosure, the term "binder pusher" refers to a
substance, which when is applied to the surface of the carbide mining insert, will cause the binder to migrate away from that surface during the sintering step, i.e. the binder is pushed in the direction
away from the surface where the "binder pusher" has been applied. The combined application of a
binder puller applied to at least one local area on the surface and a binder pusher to the at least one
different local area on the surface of the cemented carbide mining insert would mean that the green
cemented carbide mining insert could be made having a carbon content within the standardly used
ranges, such as 0.95<Com/%Co<1, and using standard processes therefore allowing for efficiency in
the production. Preferably the migration takes places through the depth of the insert, rather than
along the surface of the insert.
In one embodiment of the method the binder pusher is selected from a metal carbide, a
carbon powder, such as graphite, or a mixture thereof. The application of the metal carbide, the
carbon powder or the mixture thereof will create a carbon gradient, which will result in the cobalt
migrating away from the surface to which it was applied, i.e. the binder is pushed away from that
surface of the carbide towards the inner bulk in this local area(s). Selection of a metal carbide will
have the additional effect of grain refinement in the applied local area whereas the selection of a
carbon powder will have the effect of promoting grain growth in the applied local area(s). The
resulting difference in the grain growth gradient created is not as significant as the effect that the
binder gradient has on the hardness gradient.
In one embodiment, the binder pusher is a combination of a metal carbide and a carbon
powder. The weight ratio of the metal carbide to the carbon powder is suitable from about 0.05 to
about 50, preferably from about 0.1 to about 25, more preferably from about 0.2 to about 15 and
even more preferably from about 0.3 to about 12 and most preferably from about 0.5 to 8. The
metal carbide is suitably provided onto the surface or surfaces in an amount of from about 0.1 to
about 100 mg/cm 2, preferably in an amount of from about 1 to about 50 mg/cm2 . The carbon
powder is suitably provided onto the surface or surfaces in an amount of from about 0.1 to about
100 mg/cm 2, preferably in an amount of from about 0.5 to about 50mg/cm . 2
If only a carbon powder, such as graphite, is selected as the binder pusher this would lead to
a coarsening of the hard phase grains in the area where it has been applied. This would result in
being able to achieve a combination of high wear resistance and improved thermal conductivity in
the zones on the mining button exposed to the rock being worked and high toughness behind these
zones.
In one embodiment of the method the metal carbide is selected from a carbide of chromium, vanadium, magnesium, iron or nickel, preferably a carbide of chromium, such as Cr 3 C 2 ,
Cr 2 3C6, Cr7 C 3 .
Selection of a metal carbide, such as Cr 3 C2 , in combination with a carbon powder is
advantageous as this combination will cause the binder to migrate from the doped surface and the
addition of the carbon prevents the grain refining effect of the Cr3C 2 .
During sintering any metal carbide applied to the surface of the green cemented carbide
mining insert should substantially dissolve.
In one embodiment of the method, the binder puller and the binder pusher are applied to puller and binder pusher to different local areas a binder gradient between the two surfaces is created. This gradient in binder will mean that a hardness gradient is created, with a harder, binder depleted surface formed where the binder pusher has been applied and a tougher, binder rich surface formed where the binder puller has been applied. The combined application of a binder puller and binder pusher to different local areas of the surface of the cemented carbide mining insert is particularly useful in creating a hardness gradient in larger carbide bodies where previously known methods would not create a sufficiently deep gradient. The binder puller may be applied to a selected area on the surface of the green cemented carbide mining insert and the binder pusher may be applied to a different selected area on the surface of the green cemented carbide mining insert. The binder pusher could be placed in the wear zone to reduce the binder content and therefore improve wear resistance in that area or where it is favourable to have higher thermal conductivity. The local application of the binder puller and the binder pusher presents unique possibilities to create carbide bodies with tailor made properties.
Another benefit of using this method is that self-sharpening zones can be created if the wear
rates on different areas of the surface are uneven. The contact pressure between a worn insert and
the rock increases with a sharper tip as there is a reduced area of contact. With a homogenous
material, the wear causes the formation of a wear flat that often needs re-sharping using diamond
grinding tools. Re-sharpening by grinding is costly and requires that the drill bits are unmounted. By
having non-homogeneous material properties, it is possible to have zones that wear faster and zones that wear slower. If the material properties of the mining inserts are tailored to having a wear
surface that has areas with different wear rates, the formation of wear flats are avoided, and
consequently sharper wear surfaces are created in comparison to using homogeneous materials.
In one embodiment of the method, the binder puller and the binder pusher are applied to
substantially opposing local areas of the surface of the cemented carbide mining insert.
In one embodiment, the method of applying the binder puller and the binder pusher is
selected from pressing, dipping, painting, spraying (air brushing), stamping or 3D printing. Dipping
could be done with or without masking. The binder puller and binder pusher may be applied to the
surface of green cemented carbide mining insert in the form of liquid dispersions or a slurry. In such
as case, the liquid phase is suitably water, an alcohol or a polymer such as polyethylene glycol. The
concentration of the slurry is suitably 5-50 wt% of the powder in the liquid phase, such as 15-40
wt%. This range is advantageous so that a sufficient effect of the binder puller or pusher is realised.
If the powder content is too high, then there may be issues with clogging and lumping within the
liquid dispersion or slurry. Alternatively, they could be introduced as a solid substance, for example by adding the powder into the pressing mould in a suitable position. The powder could be mixed with a hard-phase powder, for example a WC-based powder. The binder puller and the binder pusher could also be applied to the cemented carbide mining insert in any other suitable way. The compositions and concentration of the slurry and the way it is applied influences the control of the redistribution of the binder and therefore allows the hardness profile of the cemented carbide mining insert to be controlled.
In one embodiment of the method, the binder puller is applied to a first part of the surface
(10) and the binder pusher is applied to a second part of the surface (20) rotationally symmetrically
as shown in Figure 1.
In one embodiment of the method, the binder puller is applied to a first part of the surface
(10) and the binder pusher is applied to a second part of the surface (20) rotationally asymmetrically
as shown in Figure 2.
As there is flexibility in where the binder puller and binder pusher are applied, this allows
tailoring of the position of the "wear zone", i.e. the position on the surface having the most
enhanced wear properties. For example, the wear zone could be on either the top or the side of the
insert depending where the interaction between the cemented carbide mining insert and rock being
drilled is the highest. This will vary depending on the application it is being used for and the position
of the cemented carbide mining insert on the rock drill bit.
Cemented carbide mining inserts are subjected to high compressive loading. Consequently, surface cracking caused by small cracks growing to a critical size through repeated intermittent high
loading is a common cause of insert failure. It is known that introducing compressive stress into the
surface of the insert can reduce this problem as the presence of the compressive stress can prevent
crack growth and wear of the material. Known methods of introducing compressive stress into
surfaces of a cemented carbide mining insert include shot peening, vibration tumbling and
centrifugal tumbling. These methods are all based on mechanical impact or deformation of the outer
surface of the body and will increase the lifetime of the cemented carbide mining inserts.
In one embodiment of the method, post sintering the cemented carbide mining insert is
treated with a tumbling process. The cemented carbide mining inserts are subjected to a post
treatment surface hardening which introduces high levels of compressive stress into the inserts. For
mining inserts, this would normally be a tumbling treatment, which could be centrifugal or
vibrational. However, other post-treatments surface hardening methods, e.g. shot peening, could be
used. Following tumbling, normally an increase in magnetic coercivity (kA/m) is measured.
A "standard" tumbling process would typically be done using a vibrational tumbler, such as a
Reni Cirillo RC 650, where about 30 kg inserts would be tumbled at 50 Hz for about 40 minutes. An
alternative typical "standard" tumbling process would be using a centrifugal tumbler such as the
ERBA-120 having a closed lid at the top and has a rotating disc at the bottom. Cooling water with
antioxidants is continuously fed with 5 liters per minute when the disc (0600mm) rotates. Tungsten
carbide media can also be added to increase the load in the tumbler. The rotation causes the inserts
to collide with other inserts or with any media added. The collision and sliding removes sharp edges
and causes strain hardening. For "standard" tumbling using a centrifugal tumbler the tumbling
operation would typically be run from 120 RPM for at least 20 minutes.
In one embodiment of the method, the tumbling process is a "High Energy Tumbling" (HET)
method. To introduce higher levels of compressive stresses into the cemented carbide mining insert
a high energy tumbling process may be used. There are many different possible process set ups that
could be used to introduce HET, including the type of tumbler, the volume of media added (if any),
the treatment time and the process set up, e.g. RPM for a centrifugal tumbler etc. Therefore, the
most appropriate way to define HET is in terms of "any process set up that introduces a specific
degree of deformation hardening in a homogenous cemented carbide mining insert consisting of
WC-CO, having a mass of about 20g". In the present disclosure, HET is defined as a tumbling
treatment that would introduce a hardness change, measured using HV3, after tumbling (AHV3%) of
at least:
AHV3%= 9.72- 0.00543*HV3uIk (equation1)
Wherein:
AHV3%= 100*(HV3 0 .3 mm- HV3buIk)/HV3buk (equation2)
HV3buk is an average of at least 30 indentations points measured in the innermost (centre) of
the cemented carbide mining insert and HV 3 .3mm is an average of at least 30 indentation points at
0.3mm below the tumbled surface of the cemented carbide mining insert. This is based on the
measurements being made on a cemented carbide mining insert having homogenous properties. By
"homogeneous properties" we mean that post sintering the hardness different is no more than 1%
from the surface zone to the bulk zone. The tumbling parameters used to achieve the deformation
hardening described in equations (1) and (2) on a homogenous cemented carbide mining insert
would be applied to cemented carbide bodies having a gradient property.
HET tumbling may typically be performed using an ERBA 120, having a disc size of about 600 media that is larger in size than the inserts being tumbled, or at about 200 RPM if the media used is smaller in size than the inserts being tumbled; Using a R6sler tumbler, having a disc size of about 350 mm, at about 200 RPM if the tumbling operation is either performed without media or with media that is larger in size than the inserts being tumbled, or at about 280 RPM if the media used is smaller in size than the inserts being tumbled. Typically, the parts are tumbled for at least 40-60 minutes.
HET enables use of binder enriched surface zones as the compressive stresses introduced from the
HET counteract the tensile stresses formed by the higher thermal expansion coefficient in the binder
enriched zones adjacent to binder depleted zones.
Another aspect of the present invention relates to a cemented carbide mining insert
comprising one or more hard-phase components and a binder wherein there is a hardness gradient
from a first part of the surface to a second part of the surface of the cemented carbide mining insert,
wherein the first part of the surface is substantially opposing the second part of the surface, such
that post sintering:
- the first part of the surface is between 30HV3 softer and 80HV3 harder than the second part of the
surface; and
- the first part of the surface is between 5 and 120 HV3 harder than the bulk; and
- the second part of the surface is between 20HV3 and 70HV3 harder than the bulk.
The hardness measurements are post sintering and prior to any post sintering treatment,
such as tumbling.
In one embodiment, the hardness gradient is such that:
- the first part of the surface is between 2% softer and +6% harder than the second part of the
surface; and
- the first part of the surface is between +0.5 and +10% harder than the bulk; and - the second part of the surface is between +0.3% and 6% harder than the bulk.
The first part of the surface is the surface where the binder puller has been applied to form
an oxide / carbonate doped surface. The second part of the surface is the surface opposing where
the binder puller has been applied (the side opposing the oxide / carbonate doped surface).
Optionally, the second part of the surface could be a surface where a binder pusher has been
applied to form a carbide doped surface.
This is also shown in table 1 below:
Hardness difference HV3 Hardness difference (%)
First part of the surface (oxide First part of the surface (the First part of the surface (the
/ carbonate doped surface) vs oxide / carbonate doped oxide / carbonate doped
second part of the surface surface) is between 30HV3 surface) is between 2% softer
(side opposing oxide / softer and 80HV3 harder. and 6% harder.
carbonate doped surface)
First part of the surface (oxide First part of the surface (the First part of the surface (the
/ carbonate doped surface) vs oxide / carbonate doped oxide / carbonate doped
bulk surface) is between 5HV3 and surface) is between 0.5% and
120HV3 harder than the bulk. 10% harder than the bulk.
Second part of the surface Second part of the surface (the Second part of the surface (the
(side opposing oxide / side opposing the oxide / side opposing the oxide
/ carbonate doped surface) vs carbonate doped surface) is carbonate doped surface) is
bulk between 20HV3 and 70HV3 between 0.3% and 6% harder
harder than the bulk. than the bulk.
Table 1: Hardness differences
By the term "bulk" is herein meant the cemented carbide of the innermost part (centre) of
the rock drill insert and for this disclosure is the zone having the lowest hardness.
The hardness of the cemented carbide inserts is measured using Vickers hardness mapping.
The cemented carbide bodies, are sectioned along the longitudinal axis and polished using standard procedures. Vickers indentations at a 3 kg load are then symmetrically distributed over the polished
section. The rhombuses in figures 3-13 and 16 show the locations of the HV3 indentations. The
hardness measurements are performed using a programmable hardness tester, KB30S by KB
PrOftechnik GmbH calibrated against HV3 test blocks issued by Euro Products Calibration Laboratory,
UK. Hardness is measured according to ISO EN6507.
HV3 measurements were done in the following way:
- Scanning the edge of the sample.
- Programming the hardness tester to make indentations at specified distances from the edge
of the sample.
- Indentation with 3 kg load at all programmed co-ordinates. - The computer moves the stage to each co-ordinate with an indentation and runs auto adjust
light, auto focus and the automatically measures the size of each indentation.
- The user inspects all the photos of the indentations for focus and other matters that disturb
the result.
The HV3 measurements for the oxide / carbonate doped surface and side opposing the
oxide / carbonate doped surface were measured at a distance between 0.3 and 0.8 mm below the surface, with 10-40 indentations being made and then the average HV3 measurement calculated.
The HV3 measurement for the bulk is measured in near the centre of the polished section at the position having the lowest hardness, over an area of about 1.5-2mm 2, taking the average from
about 15-20 indentations.
In one embodiment, the maximum concentration (%binder-max) is less than 20% higher
than the minimum concentration (%binder-min) within the cemented carbide mining insert.
In one embodiment, the %binder-min (e.g. minimum Co concentration / %Co-min) is at a
depth, in percentage of the total height of the sintered cemented carbide mining insert, of
between 1-50% from the first part of the surface, preferably between 5-40%. The %binder-min is
typically at a depth of 0.5-10 mm, preferably 0.8-7 mm from the first part of the surface.
In one embodiment, there are two peaks in binder concentration, one near the surface and
one in the bulk of the cemented carbide mining insert. There is a first maximum binder
concentration (%binder-max) (e.g. %Co-max) at the first part of the surface (e.g. at the oxide/
carbonate doped surface) and a second maximum binder concentration (%binder-max2) (e.g. %Co
max2) at a depth, in percentage of the total height of the cemented carbide mining insert, of between 15-75% from the first part of the surface (e.g. from the oxide / carbonate doped surface),
preferably between 20-65%. In one embodiment, %binder-maxl> %binder-max2. In an alternative
embodiment, %binder-maxl %binder-max2. The %binder-max2 is typically 2-15 mm from the
first part of the surface, preferably between 4 -12 mm. The difference in the height of the %binder
min and %binder-max2 is typically between 1.5-12 mm, preferably between 2.5-10 mm.
In one embodiment, there is a first chromium concentration maximum (%Cr-maxl) at the
first part of the surface (e.g. at the oxide/carbonate doped surface). In one embodiment, there is
additionally a second chromium concentration maximum (%Cr-max2) at the surface second part of
the surface (e.g. the surface opposing to oxide/carbonate doped surface), wherein %Cr-max>%Cr
max2. The chromium concentration minimum (%Cr-min) is located between %Cr-maxl and %Cr
max2, in the bulk of the cemented carbide mining insert. The %Cr-min is preferably at a depth, in
percentage of total height of the sintered cemented carbide mining insert, of 40-99%, more preferably at a depth of 50-98% from the first part of the surface. "At the surface" is defined as up to 0.3 mm from the surface.
The chemical concentrations within the cemented carbide mining insert are measured using
wavelength dispersive spectroscopy (WDS) along the centreline of a cross sectioned cemented carbide mining insert.
Another aspect of the present disclosure relates to the use of the cemented carbide mining
insert as described hereinbefore or hereinafter for rock drilling or oil and gas drilling.
The following examples are illustrative, non-limiting examples.
Example 1- only binder puller applied
Table 2 shows a summary of the samples analysed:
Sample Powder blend Slurry applied to surface Tumbling treatment
A 94 wt% WC + 6 wt% Co None None
B 94 wt% WC + 6 wt% Co None Standard
C 94 wt% WC + 6 wt% Co None HET
D 94 wt% WC + 6 wt% Co Carbide doped slurry None
E 94 wt% WC + 6 wt% Co Carbide doped slurry Standard
F 94 wt% WC + 6 wt% Co Carbide doped slurry HET
G (invention) 94 wt% WC + 6 wt% Co Oxide doped slurry None
H (invention) 94 wt% WC + 6 wt% Co Oxide doped slurry Standard
I (invention) 94 wt% WC + 6 wt% Co Oxide doped slurry HET
J (invention) 89 wt% WC + 11 wt% Co Oxide doped slurry None
K (invention) 89 wt% WC + 11 wt% Co Oxide doped slurry HET
Table 2: Summary of samples measured
For sample A to I in Table 2 the cemented carbide inserts were produced using a powder
blend having a composition of 94 wt% WC and 6 wt% Co. The WC powder grain size measured as
FSSS was before milling between 5 and 7 pm. The WC and Co powders were milled in a ball mill in
wet conditions, using ethanol, with an addition of 2 wt% polyethylene glycol (PEG 8000) as organic
binder (pressing agent) and cemented carbide milling bodies. After milling, the slurry was spray dried in N 2 -atmosphere and then uniaxially pressed into mining inserts having a size of about 12 mm in outer diameter (OD) and about 17-20 mm in height (sample B = 18.7mm height; sample C =
17.4mm height; sample D = 18.7mm height; sample E and F =17.4mm height; samples G, H and I=
20.2mm height) with a weight of approximately 14-17g each with a spherical dome ("cutting edge")
on the top. The inserts were ground on the negative part but leaving the dome and bottom part in
an as-sintered condition.
Samples A, B and C had no slurry applied. Samples D, E and F are examples are comparative examples where only a binder pusher, in the form of a "carbon doped slurry", was applied, using a
dipping technique, to the top, domed surface of the cemented carbide mining inserts. The carbon
doped slurry consisted of 25 wt% Cr 3 C 2 and 5 wt% graphite dispersed in water and was applied to
the cemented carbide insert so that about 60% of the total insert length was exposed to the carbide
doped slurry. Samples F, G and H are examples of the invention where only a binder puller is applied,
the samples were treated by applying an "oxide doped slurry", comprising 30 wt% Cr 3 02 and 70 wt%
PEG300, to the domed surface of the cemented carbide insert in an amount of between 0.25 -0.28
mg/mm 2 with about 60% of the total insert length exposed to the oxide slurry. All the samples were
sintered using Sinter-HIP in 55 bar Ar-pressure at 1410°C for 1 hour. For these examples, the slurry
was applied symmetrically, i.e. applied to the domed surface extending an equal distance down the
each of the sides of the insert.
Samples B, E and H were tumbled using "standard tumbling", using an ERBA-120 centrifugal
tumbler at 120 RPM for 30 minutes. Samples C, F and I were tumbled using "High energy tumbling
(HET)", using an ERBA-120 centrifugal tumbler 170 RPM or 40 minutes.
Samples J and K are examples of the invention where the cemented carbide inserts have a
higher binder content. The cemented carbide inserts were produced using a powder blend having a
composition of 89 wt% WC and 11 wt% Co. The WC powder grain size measured as FSSS was before milling between 8 and 12 pm. The WC and Co powders were milled in a ball mill in wet conditions,
using ethanol, with an addition of 2 wt% polyethylene glycol (PEG 8000) as organic binder (pressing
agent) and cemented carbide milling bodies. After milling, the slurry was spray-dried in N 2
atmosphere and then uniaxially pressed into mining inserts having a size of about 17 mm in outer
diameter (OD) and about 22 mm in height, with a weight of approximately 31 g each with a conical
tip ("cutting edge") on the top. The inserts were ground on the cylindrical part but leaving the
conical tip and the bottom part in an as-sintered condition.
Samples J and K are examples of the invention where only a binder puller is applied, the
samples were treated by applying an "oxide doped slurry", using a dipping technique, comprising 30 wt% Cr 3 02 and 70 wt% PEG300, covering the conical tip and part of the cylindrical section in an amount of between 0.25-0.35 mg/mm 2 so that approximately 75% of the total length of the insert was exposed to the oxide doped slurry. The samples were sintered using Sinter-HIP in 55 bar AR pressure at 1410°C for 1 hour. For these examples, the slurry was applied symmetrically, i.e. applied to the domed surface extending an equal distance down the each of the sides of the insert.
Samples K was tumbled using "High energy tumbling (HET)", in a R6sler model FKS 04.1 E-SA centrifugal tumbler at 250 RPM for 60 minutes with 50kg of media in the form of carbide balls of
7mm in diameter.
Figures 3-13 show the HV3 iso-hardness maps for samples A - I respectively and Figures 15
18 shows the centre lines plots for samples A-K from Table 2. The hardness profiles of the cemented
carbide inserts are as described Table 1. The binder puller was applied to the tip (30) of the
cemented carbide mining insert, as shown in figure 14.
It can be seen that the hardness profiles of the present invention are very different to the
prior art and show that there is a softer core zone in the bulk and higher hardness at both the top
and the bottom of the cemented carbide mining insert.
Example 2 - binder puller and binder pusher applied
Cemented carbide inserts were formed using the same starting material as samples J and K
(89 wt% WC + 11 wt% Co) and method as described in table 2 / example 1. Mining inserts were
formed by uni-axial pressing having a length of 24 mm and a cylindrical base of 19 mm diameter and
a spherical (half dome) tip. Two PEG slurries were made up, the first a "binder puller", which
consisted of 30%Cr 2 3+PEG and the second a "binder pusher", which consisted of
25%Cr 3C 2+5%C+PEG. The slurries were then applied to the surface of the inserts by dipping the
inserts into the slurry. The inserts were then sintered at 1410°C, 50 bar pressure in an argon
atmosphere. In this example, the two slurries were applied asymmetrically to opposing sides i.e. the
binder puller was applied to the side of the insert (10) and the binder pusher was applied opposite
(20) to this as shown in figure 2. The HV5 iso-hardness map is shown in figure 19. It can be seen that
a softer core is produced using this method, this hardness profile has been shown to provide
efficient drilling behavior. The two slurries could have alternatively been applied symmetrically as
shown in figure 1. By controlling the concentration and positioning of the application of the two
slurries this facilitates the ability to be able to tailor the redistribution of the binder phase to meet
the needs of the application.
Example 3 - Insert compression test
The toughness of drill bit inserts of samples B, C, E, F, H and I described in table 2 / example
1 were characterized using an insert compression (IC) test. The IC test method involves compressing
a drill bit insert between two plane-parallel hard counter surfaces, at a constant displacement rate,
until the failure of the insert. A test fixture based on the ISO 4506:2017 (E) standard "Hardmetals
Compression test" was used, with cemented carbide anvils of hardness exceeding 2000 HV, while the test method itself was adapted to toughness testing of rock drill inserts. The fixture was fitted
onto an Instron 5989 test frame.
The loading axis was identical with the axis of rotational symmetry of the inserts. The
counter surfaces of the fixture fulfilled the degree of parallelism required in the ISO 4506:2017 (E)
standard, i.e. a maximum deviation of 0.5 pm / mm. The tested inserts were loaded at a constant
rate of crosshead displacement equal to 0.6 mm / min until failure, while recording the load
displacement curve. The compliance of the test rig and test fixture was subtracted from the
measured load-displacement curve before test evaluation. Three inserts were tested per sample
type. The counter surfaces were inspected for damage before each test. Insert failure was defined to take place when the measured load suddenly dropped by at least 1000 N. Subsequent inspection of
tested inserts confirmed that this in all cases this coincided with the occurrence of a macroscopically
visible crack. The material toughness was characterized by means of the total absorbed deformation
energy until fracture. The results of the insert compression test are shown in Table 3:
Sample Deformation energy until fracture (J)
B 7.37
C 8.87
E 7.27
F 9.96
H (invention) 9.75
I (invention) 12.50
Table 3: Summary of Insert compression test results
The toughness of the samples treated according to the method the present invention is
higher than samples known in the prior art according to the IC test results when comparing samples
that were tumbled in the same way.
Example 4 - Pendulum Hammer
For the Pendulum Hammer test cemented carbide mining inserts with a dome shaped tip of
5.0 mm radius and a diameter of 10.0 mm were produced and treated in the same way samples B, C,
E, F, H and I as described in example 1. A schematic drawing of the pendulum hammer test set-up is
shown in figure 20. The inserts were firmly mounted into a holder (30) with only the dome section
protruding. On the pendulum (40) a hard-counter surface is mounted (50) on the pendulum hammer head. The counter surface used was a polished plate (h = 5.00 mm, I = 19.40 mm, w = 19.40 mm) of a
hard, fine grained hard metal grade having a Vickers hardness of approx. 1900 HV30. When the
pendulum is released, the counter surface hits the sample tip. If the sample fails, the impact energy
(E) absorbed by the sample measured in Joules (J) is not recorded. For a given initial pendulum
angle, the impact energy is calculated using equation 3 where m is the total mass of the pendulum
hammer 4.22 kg, g is the gravitational constant 9.81 m/s2, L is the pendulum hammer length 0.231
m and a is the angle in radians.
E= (mtot x g x L x (1-cos (a)) (equation 3)
To determine the energy needed to fracture the sample, it is first impacted by the pendulum
released from a suitable low angle. The angle is then increased step-wise with a 5 degree step until
the sample fails. Following this, inserts from the same sample are impacted at a 3 degree lower
angle than the impact angle that caused the failure and the test is repeated with smaller incremental
increases in the impact angle. The angle where the insert does not break is recorded and the
corresponding impact energy calculated. In these tests, the counter surface was exchanged every 5
10 impacts. The results are shown in table 4 below:
Sample Impact energy (J)
B 6.9
C 10.3
E 6.0
F 8.3
H (invention) 7.7
I (invention) 15.0
Table 4: Summary of Pendulum Hammer test results
The results show that there is a significant increase in the impact resistance for the sample
produced using the method of the current invention when comparing samples tumbled in the
equivalent way.
Example 5 - Chemical analysis
The chemical gradient of the sample was investigated by means of wavelength dispersive
spectroscopy (WDS) analysis using a Jeol JXA-8530F microprobe. Line scans along the centre line
were done on cross sections of the sintered materials, prior to tumbling for samples D (comparison)
and G (invention) as described in table 2 / example 1. Samples were prepared by precision cutter,
followed by mechanical grinding and polishing. The final step of the sample preparation was carried out by polishing with 1 m diamond paste on a soft cloth. An acceleration voltage of 15kV was used
to perform line scans with a step size of 100pm and a probe diameter of 100pm. Three line scans per
sample were carried out and the average is reported. The cobalt concentration profiles are
compared in figure 21, the chromium concentration profiles are compared in figure 22 and the Cr/Co
concentration profiles are compared in figure 23.
For comparison with a cemented carbide mining insert having a higher binder concentration,
line scans along the centre line were done on cross sections of sample K post tumbling. Tumbling is
assumed not to affect the chemical composition nor the WDS analysis. The lines scans for the Co
concentration and the Cr concentration are shown respectively in figures 24 and 25.
It can be seen that for the samples produced according to the method of this invention that
the highest Co concentration can be found in the tip and the bulk of the cemented carbide insert;
and the lowest Cr concentration and lowest Cr/Co concentration is found in the bulk of the
cemented carbide insert.
Example 6 - Field trial
Cemented carbide inserts C (comparison), F (comparison) and I (invention) were tested in a
field trail at the Sandvik test mine in Tampere, Finland drilling granodiorite (granite with quartsite).
Drill bits were made using six gage inserts and three front inserts per bit. The gauge inserts had a sintered diameter of 10 mm and a height of 16.6 mm. The front inserts had a sintered
diameter of 9 mm and a height of 13.8. All the inserts had a spherical dome tip. In the test, the wear
on the gauge inserts was compared as this is the most crucial part of the bit in terms of bit lifetime.
Therefore, the front inserts for all bits were made using a standard cemented carbide according to
example 1 sample C and the gauge inserts were varied in their composition to assess the effect of
composition on wear.
The test was performed using a hydraulic HFX5 top hammer drill rig from Sandvik Tamrock
with a working pressure of 210 bar, a feed pressure of 90 bar, a rotation of 230 rpm with a rotation
pressure of 70 bar.
The diameters of the gauge inserts were measured using a sliding caliper as function of
drilled depth, measured approximately every 50 m. Two bits with C inserts, one bit with F inserts and
three bits with I inserts were recovered. The greater change in diameter is an indication of greater wear. The change in diameter as a function of drilling depth is shown in figure 26 and a summary of
meters drilled as a function of diameter loss is shown in table 5 below:
Sample Initial bit diameter Meters Final bit Meters drilled per
(mm) drilled diameter (mm) diameter loss (m/mm)
C -5 49.7 387 47.9 215
C -6 49.7 354 48.2 236
F-4 49.8 239 49.0 299
1- 1 49.6 389 48.5 354
(invention)
1-2 49.6 352 48.6 352
(invention)
1-3 49.6 450 48.3 346
(invention)
Table 5: Summary of field trial results showing change in diameter as a function of drilling depth
It can clearly be seen that meters drilled per mm of diameter change is greater for the
inventive inserts (I) compared to the comparative inserts (C and F), with the inventive inserts (1)
having a 55% increase in wear resistance compared to comparative inserts (C) and a 32% increase in
wear resistance compared to comparative inserts (F).
Claims (10)
1. A method of redistributing the binder phase of a cemented carbide mining insert comprising a
WC hard-phase component, optionally one or more further hard-phase components and a binder comprising the steps of:
a) providing a green cemented carbide mining insert;
b) applying at least one binder puller selected from a metal oxide or a metal carbonate to the surface of the green cemented carbide mining insert; and
c) sintering the green carbide mining insert;
wherein the metal oxide or metal carbonate is applied to a local area on the surface of the green
cemented carbide at the top of mining insert in the form of a liquid dispersion or a slurry; and
wherein post sintering the cemented carbide mining insert is treated with a "High Energy
Tumbling" process, wherein post tumbling a homogenous cemented carbide mining insert has been deformation hardened such that AHV3%> 9.72 - 0.00543*HV3buk.
2. The method according to claim 1 wherein the binder puller is Cr 20 3 .
3. The method according to claim 1 or claim 2 further comprising the step between steps b) and c) of:
applying at least one binder pusher, selected from a metal carbide, a carbon powder or a
mixture thereof, to at least one different local area on the surface of the cemented carbide mining
insert.
4. The method according to any one of the previous claims, wherein the binder puller and the
binder pusher are applied to substantially opposing local areas of the surface of the green
cemented carbide mining insert.
5. The method according to any one of the previous claims, wherein the binder puller and the
binder pusher are applied symmetrically.
6. The method according to any one of the previous claims, wherein the binder puller and binder
pusher are applied asymmetrically.
7. A cemented carbide mining insert comprising one or more hard-phase components and a binder wherein there is a hardness gradient from a first part of the surface to a second part of the surface of the cemented carbide mining insert, wherein the first part of the surface is substantially opposing the second part of the surface, such that post sintering:
- the first part of the surface is between 30HV3 softer and 80HV3 harder than the second part of the surface; and
- the first part of the surface is between 5 and 120 HV3 harder than the bulk; and
- the second part of the surface is between 20HV3 and 70HV3 harder than the bulk;
and wherein there is a minimum concentration (%binder-min) within the cemented carbide mining insert at a depth, in percentage of the total height of the sintered cemented carbide mining insert, of between 0.5-10 mm from the first part of the surface.
8. A cemented carbide mining insert according to claim 7, wherein
the maximum binder concentration (%binder-max) is less than 20% higher than the minimum concentration (%binder-min) within the cemented carbide mining insert.
9. A cemented carbide mining insert according to claim 7 or claim 8, wherein the %binder-min is at a depth, in percentage of the total height of the sintered cemented carbide mining insert, of between 1-50% from the first part of the surface.
10. A cemented carbide mining insert according to any one of claims 7-9, wherein:
- there is a first binder concentration maximum (%binder-max) at the first part of the surface; and
- there is a second binder concentration maximum (%binder-max2) at a depth, in percentage of the total height of the sintered cemented carbide mining insert, of between 15-75% from the first part of the surface.
11. A cemented carbide mining insert according to any one of claims 7-10, wherein there is a first chromium concentration maximum (%Cr-max) at the first part of the surface.
12. A cemented carbide mining insert according to claim 11, wherein there is additionally a second chromium concentration maximum (%Cr-max2) at the second part of the surface;
- %Cr-max1>%Cr-max2; and
- there is a chromium concentration minimum (%Cr-min) located between %Cr-maxl and %Cr max2.
13. A cemented carbide mining insert according to claim 12, wherein the %Cr-min is at depth, in
percentage of the total height of the sintered cemented carbide mining insert, of between 40-99%, from first part of the surface.
Figure 1 20
10
20
Figure 2
1/13
A 1440
10
1440 1440 5
0
-10 -5 0 5 Figure 3
(mm)
B
10
1430 5
0
-10 -5 0 5 Figure 4 (mm)
2/13
C 10 1450
1440 1420 5 1430 1430 1450
0
-5 0 5 Figure 5 (mm)
D 10 1490
1450 1390 1350 5 1430
1.490
0
-5 0 5
(mm) Figure 6
3/13
E
10
1480 1440 5 1400
0
-5 0 5 Figure 7 (mm)
F
10 1500 1380
5 1460 1420
0
-5 0 5 Figure 8 (mm)
4/13
G 10
1490
1450 1490 5
1490 1530 0
-5 0 5 Figure 9
(mm)
H 10
1550 1510
5 1450
1510 0
-5 0 5 Figure 10 (mm) 5/13
-5 0 5 Figure 11 (mm)
15 J
1120 1120
1110 10
1110 1090 1100 5 100
1090 1110
1120 0
-10 -5 0 5 Figure 12 (mm) 6/13
K
1.120
10 1.130 1.100
5
1130
0
-10 -5 0 5
(mm) Figure 13
30
Figure 14
7/13
A B 1500 C
1450
1400
1350
0 5 10 15 Depth below tip (mm) Figure 15
1550
D E 1500 F
1450
1400
1350
0 5 10 15 Depth below tip (mm) Figure 16
8/13
G H 1500
1450
1400
1350
0 5 10 15
Depth below tip (mm) Figure 17
1140 J K
1120
1100
1080 0 5 10 15
Depth below tip (mm) Figure 18
9/13
(mm)
19
a B A
Figure 20
10/13
7,5
D 7,0 G 6,5
6,0
5,5
5,0
4,5 0 5 10 15 Depth below tip (mm) Figure 21
0,25
D G 0,20
0,15
0,10
0,05 0 5 10 15
Depth below tip (mm) Figure 22
11/13
0,05
G D 0,04
0,03
0,02
0,01
0 5 10 15 Depth below tip (mm) Figure 23
13
K
12
11
10 0 5 10 15 Depth below tip (mm) Figure 24
12/13
0,20
K 0,15
0,10
0,05
0,00 0 5 10 15 Depth below tip (mm) Figure 25
0,0
+ + -0,5
Data Linear Bit -1,0 points fit
C-5 C-6 *
F-4 -1,5 I-1
I-2
I-3
0 100 200 300 400 Drilled meters (m) Figure 26
13/13
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP18206093.9A EP3653743A1 (en) | 2018-11-14 | 2018-11-14 | Binder redistribution within a cemented carbide mining insert |
| EP18206093.9 | 2018-11-14 | ||
| PCT/EP2019/080305 WO2020099197A1 (en) | 2018-11-14 | 2019-11-06 | Binder redistribution within a cemented carbide mining insert |
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| EP3909707B1 (en) * | 2020-05-14 | 2024-11-06 | Sandvik Mining and Construction Tools AB | Method of treating a cemented carbide mining insert |
| CN113549800A (en) * | 2021-05-13 | 2021-10-26 | 厦门大鸿翰金属材料科技有限公司 | High-performance superfine hard alloy and preparation method thereof |
| EP4104952A1 (en) * | 2021-06-16 | 2022-12-21 | Sandvik Mining and Construction Tools AB | Cemented carbide insert with eta-phase core |
| JP2024527394A (en) * | 2021-07-14 | 2024-07-24 | サンドヴィック マイニング アンド コンストラクション ツールズ アクティエボラーグ | Cemented carbide inserts for mining or cutting applications containing gamma phase carbides |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS52110209A (en) * | 1976-03-15 | 1977-09-16 | Mitsubishi Metal Corp | Coated hard alloy tool |
| JP2757469B2 (en) * | 1989-07-06 | 1998-05-25 | 三菱マテリアル株式会社 | Tungsten carbide based cemented carbide end mill |
| JP2762745B2 (en) * | 1989-12-27 | 1998-06-04 | 住友電気工業株式会社 | Coated cemented carbide and its manufacturing method |
| JP3366659B2 (en) * | 1991-12-16 | 2003-01-14 | 東芝タンガロイ株式会社 | Heterogeneous layer surface-finished sintered alloy and method for producing the same |
| DE69310568T2 (en) * | 1992-02-20 | 1998-01-22 | Mitsubishi Materials Corp | Carbide alloy |
| US5623723A (en) * | 1995-08-11 | 1997-04-22 | Greenfield; Mark S. | Hard composite and method of making the same |
| AT5837U1 (en) * | 2002-04-17 | 2002-12-27 | Plansee Tizit Ag | HARD METAL COMPONENT WITH GRADED STRUCTURE |
| US7258833B2 (en) * | 2003-09-09 | 2007-08-21 | Varel International Ind., L.P. | High-energy cascading of abrasive wear components |
| SE526601C2 (en) * | 2003-12-15 | 2005-10-18 | Sandvik Intellectual Property | Cemented carbide tool for metal cutting or metal forming, has main body with surface portion having smaller Wc grain size than interior portion and lower binder phase content than interior portion |
| JP5448300B2 (en) * | 2003-12-15 | 2014-03-19 | サンドビック インテレクチュアル プロパティー アクティエボラーグ | Cemented carbide tool for mining and construction, and manufacturing method thereof |
| DE602004012521T8 (en) * | 2003-12-15 | 2009-08-13 | Sandvik Intellectual Property Ab | Cemented carbide insert and method for its production |
| SE532704C2 (en) * | 2008-03-31 | 2010-03-23 | Atlas Copco Secoroc Ab | Procedure for increasing the toughness of pins for a rock drill tool. |
| FR2936817B1 (en) * | 2008-10-07 | 2013-07-19 | Varel Europ | PROCESS FOR MANUFACTURING A WORKPIECE COMPRISING A BLOCK OF DENSE MATERIAL OF THE CEMENT CARBIDE TYPE, HAVING A LARGE NUMBER OF PROPERTIES AND PIECE OBTAINED |
| AU2013273604B2 (en) * | 2008-11-11 | 2015-12-03 | Sandvik Intellectual Property Ab | Cemented carbide body and method |
| EP2184122A1 (en) * | 2008-11-11 | 2010-05-12 | Sandvik Intellectual Property AB | Cemented carbide body and method |
| US9234391B2 (en) * | 2011-11-29 | 2016-01-12 | Smith International, Inc. | Shear cutter with improved wear resistance of WC-CO substrate |
| AU2016265198A1 (en) * | 2015-05-21 | 2017-11-09 | Sandvik Intellectual Property Ab | A method of producing a tool for cutting, drilling or crushing of solid material, and such a tool |
| EP3423221B1 (en) * | 2016-02-29 | 2024-08-07 | Sandvik Intellectual Property AB | Cemented carbide with alternative binder |
| KR102457545B1 (en) * | 2016-09-28 | 2022-10-20 | 산드빅 인터렉츄얼 프로퍼티 에이비 | rock drilling insert |
-
2018
- 2018-11-14 EP EP18206093.9A patent/EP3653743A1/en not_active Withdrawn
-
2019
- 2019-11-06 MX MX2021005689A patent/MX2021005689A/en unknown
- 2019-11-06 US US17/293,572 patent/US20220001445A1/en not_active Abandoned
- 2019-11-06 PE PE2021000520A patent/PE20210941A1/en unknown
- 2019-11-06 WO PCT/EP2019/080305 patent/WO2020099197A1/en not_active Ceased
- 2019-11-06 EP EP19798621.9A patent/EP3880858A1/en active Pending
- 2019-11-06 AU AU2019380489A patent/AU2019380489B2/en active Active
- 2019-11-06 JP JP2021524270A patent/JP7532357B2/en active Active
- 2019-11-06 CA CA3115189A patent/CA3115189A1/en active Pending
- 2019-11-06 CN CN201980071987.7A patent/CN113039304A/en active Pending
-
2021
- 2021-05-06 CL CL2021001197A patent/CL2021001197A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX2021005689A (en) | 2021-09-28 |
| AU2019380489A1 (en) | 2021-05-27 |
| EP3880858A1 (en) | 2021-09-22 |
| WO2020099197A1 (en) | 2020-05-22 |
| PE20210941A1 (en) | 2021-05-21 |
| US20220001445A1 (en) | 2022-01-06 |
| JP7532357B2 (en) | 2024-08-13 |
| CA3115189A1 (en) | 2020-05-22 |
| JP2022512933A (en) | 2022-02-07 |
| CL2021001197A1 (en) | 2021-10-22 |
| BR112021009272A2 (en) | 2021-08-10 |
| CN113039304A (en) | 2021-06-25 |
| EP3653743A1 (en) | 2020-05-20 |
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