Patent Application
20140284115
This disclosure relates to a polycrystalline diamond construction formed of polycrystalline diamond (PCD) material, a method for making the same and tools comprising the same, particularly but not exclusively for use in boring into the earth.
Polycrystalline diamond (PCD) material comprises a mass of inter-bonded diamond grains and interstices between the diamond grains. A body of PCD material may be made by subjecting an aggregated mass of diamond grains to a high pressure and temperature in the presence of a sintering aid which is typically a metal such as cobalt, nickel, iron or an alloy containing one or more such metals and which may promote the inter-bonding of diamond grains. The sintering aid may also be referred to as a catalyst material for diamond and/or a binder material. Interstices within the sintered PCD material may be wholly or partially filled with residual catalyst material. PCD may be formed on a substrate, such as a cobalt-cemented tungsten carbide substrate, which may provide a source of cobalt catalyst material for the PCD.
PCD material may be used as an abrasive compact in a wide variety of tools for cutting, machining, milling, grinding, drilling or degrading hard or abrasive materials such as rock, metal, ceramics, composites and wood-containing materials. For example, tool inserts comprising PCD material are widely used within drill bits which are used for boring into the earth in the oil and gas drilling industry.
In many of these applications, the temperature of the PCD material may become elevated as it engages rock or other workpieces or bodies. Mechanical properties of PCD material such as abrasion resistance, hardness and strength tend to deteriorate at elevated temperatures, which may be promoted by the residual catalyst material within the body of PCD material.
It is desirable to improve the abrasion resistance of a body of PCD material when used as an abrasive compact in tools such as those mentioned above, as this allows extended use of the cutter, drill or machine in which the abrasive compact is located. This is typically achieved by manipulating variables such as average diamond particle/grain size, overall binder content, particle density and the like.
For example, it is well known in the art to increase the abrasion resistance of an ultrahard composite by reducing the overall grain size of the component ultrahard particles. Typically, however, as these materials are made more wear resistant they become more brittle or prone to fracture.
Abrasive compacts designed for improved wear performance will therefore tend to have poor impact strength or reduced resistance to spalling. This trade-off between the properties of impact resistance and wear resistance makes designing optimised abrasive compact structures, particularly for demanding applications, inherently self-limiting.
Additionally, because finer grained structures will typically contain more solvent/catalyst or metal binder, they tend to exhibit reduced thermal stability when compared to coarser grained structures. This reduction in optimal behaviour for finer grained structures can cause substantial problems in practical applications where the increased wear resistance is nonetheless required for optimal performance.
Prior art methods to solve this problem have typically involved attempting to achieve a compromise by combining the properties of both finer and coarser ultrahard particle grades in various manners within the ultrahard abrasive body.
Another conventional solution is to remove, for example by acid leaching, the catalyst/solvent or binder phase from the PCD material. However, it is typically extremely difficult and time consuming to remove the bulk of a metallic catalyst/solvent effectively from a PCD table, particularly from the thicker PCD tables required by current applications. Achieving appreciable leaching depths can take so long as to be commercially unfeasible or require undesirable interventions such as extreme acid treatment or physical drilling of the PCD tables.
The development of an abrasive compact that may achieve improved properties of impact and fatigue resistance consistent with coarser grained materials, whilst still retaining good wear resistance and reduced incidence of cracking is highly desirable.
Viewed from a first aspect there is provided a polycrystalline diamond construction comprising a body of polycrystalline diamond material formed of:
Viewed from a second aspect there is provided a polycrystalline diamond construction comprising a body of polycrystalline diamond material formed of:
Viewed from a third aspect there is provided a polycrystalline diamond construction comprising a body of polycrystalline diamond material formed of:
Viewed from a fourth aspect there is provided a polycrystalline diamond construction comprising a body of polycrystalline diamond material formed of:
Viewed from a fifth aspect there is provided a method for making a polycrystalline diamond construction as described above, the method comprising:
Non-limiting embodiments will now be described by way of example and with reference to the accompanying drawings in which:
a and 10b are schematic diagrams of processed images (shown in negative) of a micrograph of a polished section of an embodiment of a body of PCD material at different diamond densities.
As used herein, “polycrystalline diamond” (PCD) material comprises a mass of diamond grains, a substantial portion of which are directly inter-bonded with each other and in which the content of diamond is at least about 80 volume percent of the material. As used herein, “interstices” or “interstitial regions” are regions between the diamond grains of PCD material. In some embodiments, the interstices or interstitial regions in the PCD material may be substantially or partially filled with a material other than diamond such as a binder material comprising a catalyst for diamond, or they may be substantially empty. The PCD material may comprise one or more regions from which catalyst material has been removed from the interstices, leaving interstitial voids between the diamond grains.
As used herein, a “PCD structure” comprises a body of PCD material.
As used herein, a “metallic” material is understood to comprise a metal in unalloyed or alloyed form and which has characteristic properties of a metal, such as high electrical conductivity.
As used herein, “catalyst material” for diamond, which may also be referred to as solvent/catalyst material for diamond, means a material that is capable of promoting the growth of diamond or direct diamond-to-diamond inter-growth between diamond grains at a pressure and temperature condition at which diamond is thermodynamically stable.
A filler or binder material is understood to mean a material that wholly or partially fills pores, interstices or interstitial regions within a polycrystalline structure.
A multi-modal size distribution of a mass of grains is understood to mean that the grains have a size distribution with more than one peak, each peak corresponding to a respective “mode”. Multimodal polycrystalline bodies may be made by providing more than one source of a plurality of grains, each source comprising grains having a substantially different average size, and blending together the grains or particles from the sources. In some embodiments, the PCD structure may comprise diamond grains having a multimodal distribution.
As used herein, the term ‘total binder area’ is expressed as the percentage of non-diamond phase(s) in the total cross-sectional area of a polished cross section of the body of PCD material being analysed.
As used herein, the nearest neighbour distance between non-diamond phase grains/particles is considered to be the distance from one grain or particle to the closest non-diamond phase grain or particle.
With reference to
An example of a method for producing the PCD compact 20 comprising the body of PCD material 22, as shown in
With further reference to
In some examples, a pre-sinter assembly for making a PCD or PCBN construction, for example, may be prepared and provided in situ at the first pressure P1 as follows. A cup may be provided into which an aggregation comprising a plurality of diamond or CBN grains and a substrate may be assembled, the interior shape of the cup being generally that of the desired shape of the PCD or PCBN structure (having regard to likely distortion during the sintering step). The aggregation may comprise substantially loose diamond or CBN grains or diamond- or CBN-containing pre-cursor structures such as granules, discs, wafers or sheets. The aggregation may also include catalyst material for diamond, matrix material for PCBN, or pre-cursor material for catalyst or matrix material, which may be admixed with the diamond or CBN grains and or deposited on the surfaces of the diamond or CBN grains. The diamond or CBN grains may have a mean size of at least about 0.1 micron and or at most about 75 microns and may be substantially mono-modal or multi-modal. The aggregation may also contain additives for reducing abnormal diamond or CBN grain growth or the aggregation may be substantially free of catalyst material or additives. Alternatively or additionally, another source of catalyst or matrix material such as cobalt may be provided, such as the binder material in a cemented carbide substrate. A sufficient quantity of the aggregation may be placed into the cup and then the substrate may inserted into the cup with a proximate end pushed against the aggregation. The pre-sinter assembly comprising the aggregation and the substrate may be encased within a metal jacket comprising the cup, subjected to a heat treatment to burn off organic binder that may be comprised in the aggregation, and encapsulated within a housing (which may be referred to as a capsule) suitable for an ultra-high pressure press. The housing may be placed in a suitable ultra-high pressure press apparatus and subjected to a sinter pressure and sinter temperature to form the assembly comprising a PCD or PCBN structure adjacent the substrate, connected by a thin film of molten binder comprising cobalt. In examples such as these, the sinter pressure may be regarded as the first pressure P1.
In an example arrangement, a pre-sinter assembly for making a PCD or PCBN construction may be prepared and provided in a press apparatus at the first pressure P1 as follows. A PCD or PCBN structure may be provided pre-sintered in a previous ultra-high pressure, high temperature process. The PCD or PCBN structure may contain binder or matrix material comprising cobalt, located in interstitial regions between the diamond or CBN grains comprised in the PCD or PCBN material. In the case of PCD material, the PCD structure may have at least a region substantially free of binder material. For example, the PCD structure may have been treated in acid to remove binder material from the interstices at least adjacent a surface of the PCD structure or throughout substantially the entire volume of the PCD structure (or variations between these possibilities), leaving at least a region that may contain pores or voids. In some examples, voids thus created may be filled with a filler material that may or may not comprise binder material. The PCD or PCBN structure may be placed against a substrate and the resulting pre-construction assembly may be encased within a housing suitable for an ultra-high pressure press. The housing may be placed in a suitable ultra-high pressure press apparatus and the subjected to the first pressure P1 at a temperature at which the binder material is in the liquid state (at a condition in region D of
Example methods for making an example PCD construction will be described below with reference to
In some examples, a pre-sinter assembly may be provided, comprising an aggregation of a plurality of diamond grains located adjacent a surface of a substrate comprising cobalt-cemented tungsten carbide. The diamond grains may have a mean size in the range of about 0.1 to about 40 microns. The pre-sinter assembly may be encapsulated within a capsule for an ultra-high pressure press apparatus, into which the capsule may be loaded. The capsule may be pressurised at ambient temperature to a pressure of at least about 6.5 gigapascals and heated to a temperature in the range of about 1,500 to about 1,600 degrees Celsius, substantially greater than the melting point (at the pressure) of the cobalt-based binder material comprised in the substrate and causing the cobalt material to melt. At this temperature the pre-sinter assembly may be at a first pressure P1 in the range from about 7.5 to about 10 gigapascals (P1 may be somewhat higher than 7 gigapascals at least partly as a result of the increase in temperature). The first pressure P1 and the temperature may be substantially maintained for at least about 1 minute, or in any event sufficiently long to sinter together the diamond grains (in these examples, the sinter pressure will be substantially P1). The pressure may then be reduced from first pressure P1 through a second pressure P2 in the range from about 5.5 to about 8.5 gigapascals. The second pressure may be the pressure at which the binder material begins to solidify as the temperature is reduced through its solidification temperature.
The temperature of the pre-sinter assembly may be reduced simultaneously with pressure, provided that it remains greater than the temperature at which the cobalt-based binder material will have completely solidified. As the pressure is reduced from P2, the temperature may also be reduced through the solidification line of the cobalt-based binder material, resulting in the solidification of the binder material. In these particular examples, the pressure is substantially continuously reduced from the first pressure P1, through the second pressure P2 and through the pressure(s) at which the binder material solidifies, without substantial pause. The rate of reduction of the pressure and or temperature may be varied or the rate of the reduction of either or both may be substantially constant, at least until the cobalt-based binder material has solidified. The temperature may also be reduced substantially continuously at least until it is sufficiently low for substantially all the cobalt-based binder material to have solidified. The temperature and pressure may then be reduced to ambient conditions, the capsule removed from the ultra-high pressure press apparatus and the construction removed from the capsule. The construction may comprise a sintered PCD structure formed joined to the substrate, the PCD structure having become joined to the substrate in the same general step in which the PCD material was formed by the sintering together of the plurality of diamond grains. A thin layer rich in cobalt will be present between the PCD structure and the substrate, joining together these structures.
In a particular example method illustrated in
In a particular example method illustrated in
In a particular example method illustrated in
In a particular example method illustrated in
In the example method illustrated in
Note that the line S-L in
The method used to measure the pressure and temperature cycles as illustrated in
In some embodiments, the binder material may include one or more of phase(s) containing aluminium, silicon, cobalt, molybdenum, tantalum, niobium, nickel, titanium, chromium, tungsten, yttrium, carbon and iron. The binder material may include powder with uniform solid solution of more than one of aluminium, silicon, cobalt, nickel, titanium, chromium, tungsten, yttrium, molybdenum, niobium, tantalum, carbon and iron.
Various kinds of ultra-high pressure presses may be used, including belt-type, tetrahedral multi-anvil, cubic multi-anvil, walker-type or torroidal presses. The choice of press type is likely to depend on the volume of the super-hard construction to be made and the pressure and temperature desired for sintering the super-hard material. For example, tetrahedral and cubic presses may be suitable for sintering commercially viable volumes of PCD and PCBN material at pressures of at least about 7 gigapascals or at least about 7.7 gigapascals.
Some example methods may include subjecting a PCD construction to a heat treatment at a temperature of at least about 500 degrees Celsius, at least about 600 degrees Celsius or at least about 650 degrees Celsius for at least about 5 minutes, at least about 15 minutes or at least about 30 minutes. In some embodiments, the temperature may be at most about 850 degrees Celsius, at most about 800 degrees Celsius or at most about 750 degrees Celsius. In some embodiments, the PCD structure may be subjected to the heat treatment for at most about 120 minutes or at most about 60 minutes. In one embodiment, the PCD structure may be subjected to the heat treatment in a vacuum. For example, U.S. Pat. No. 6,517,902 discloses a form of heat treatment for pre-form elements having a facing table of PCD bonded to a substrate of cemented tungsten carbide with a cobalt binder. The substrate includes an interface zone with at least 30 percent by volume of the cobalt binder in a hexagonal close packed crystal structure.
As used herein, the thickness of the PCD structure 22, 200 or the substrate 30, 300 or some part of the PCD structure or the substrate is the thickness measured substantially perpendicularly to the interface 24. In some embodiments, the PCD structure, or body of PCD material 22, 200 may have a generally wafer, disc or disc-like shape, or be in the general form of a layer. In some embodiments, the PCD structure 22, 200 may have a thickness of at least about 0.3 mm, at least about 0.5 mm, at least about 0.7 mm, at least about 1 mm, at least about 1.3 mm or at least about 2 mm. In one embodiment, the PCD structure 22, 200 may have a thickness in the range from about 2 mm to about 3 mm.
In some embodiments, the substrate 30, 300 may have the general shape of a wafer, disc or post, and may be generally cylindrical in shape. The substrate 30, 300 may have, for example, an axial thickness at least equal to or greater than the axial thickness of the body of PCD material 22, 200 and may be for example at least about 1 mm, at least about 2.5 mm, at least about 3 mm, at least about 5 mm or even at least about 10 mm in thickness. In one embodiment, the substrate 30, 300 may have a thickness of at least 2 cm.
The PCD structure 22, 200 may be joined to the substrate 30, 300 for example only on one side thereof, the opposite side of the PCD structure not being bonded to the substrate 30, 300.
In some embodiments, the largest dimension of the body of PCD material 22, 200 is around 6 mm or greater, for example in embodiments where the body of PCD material is cylindrical in shape, the diameter of the body is around 6 mm or greater.
In some versions of the method, prior to sintering, the aggregated mass of diamond particles/grains may be disposed against the surface of the substrate generally in the form of a layer having a thickness of least about 0.6 mm, at least about 1 mm, at least about 1.5 mm or even at least about 2 mm. The thickness of the mass of diamond grains may reduce significantly when the grains are sintered at an ultra-high pressure.
Whilst not wishing to be bound by a particular theory, the method may result in a reduced likelihood or frequency of cracking of super-hard constructions because the residual stress within the construction is reduced by sufficiently reducing the applied pressure before reducing the temperature of the construction to solidify the binder material.
Non-limiting examples are described in more detail below.
A PCD insert for a rock-boring drill bit was made as described below.
A pre-sinter assembly was prepared, comprising an aggregation of a plurality of diamond grains disposed against a proximate end of a generally cylindrical cemented carbide substrate. The aggregation comprised a plurality of wafers comprising diamond grains dispersed within an organic binder material, the diamond grains having a mean size of at least about 15 microns and at most about 30 microns. The substrate comprised about 90 weight percent WC grains cemented together by a binder material comprising Co. The pre-sinter assembly was enclosed in a metal jacket and heated to burn off the organic binder comprised in the wafers, and the jacketed, pre-sinter assembly was encapsulated in a capsule for an ultra-high pressure, high temperature multi-anvil press apparatus.
The pre-sinter assembly was subjected to a pressure of about 7.7 gigapascals and a temperature of about 1,550 degrees Celsius to sinter the diamond grains directly to each other to form a layer of PCD material connected to the proximate end of the substrate by a film of molten binder material comprising cobalt from the substrate. The pressure was reduced to about 5.5 gigapascals and the temperature was reduced to about 1,450 degrees Celsius, maintaining conditions at which the diamond comprised in the PCD is thermodynamically stable (in relation to graphite, a softer allotrope of carbon) and at which the binder material is in the liquid phase. The temperature was then reduced to about 1,000 degrees Celsius to solidify the binder material and form a construction comprising the layer of PCD bonded to the substrate by the solidified binder material, and the pressure and temperature were then reduced to ambient conditions.
The construction was subjected to a heat treatment at 660 degrees Celsius for about 2 hours at substantially ambient pressure in a substantially non-oxidising atmosphere, and then cooled to ambient temperature. No cracks were evident in the PCD layer after the heat treatment.
The construction was processed by grinding and polishing to provide an insert for a rock-boring drill bit.
For comparison, a reference construction was made as follows. A pre-sinter assembly was prepared as described above in relation to the example pre-sinter assembly. The pre-sinter assembly was subjected to a pressure of about 7.7 gigapascal and a temperature of about 1,550 degrees Celsius to sinter the diamond grains directly to each other to form a layer of PCD material connected to the proximate end of the substrate by a film of molten binder material comprising cobalt from the substrate. The temperature was reduced to about 1,000 degrees Celsius to solidify the binder material and form a construction comprising the layer of PCD bonded to the substrate by the solidified binder material, and then the pressure and temperature were reduced to ambient conditions. The construction was subjected to a heat treatment at 660 degrees Celsius for about 2 hours at substantially ambient pressure in a substantially non-oxidising atmosphere, and then cooled to ambient temperature. Severe cracks were evident at the side of the PCD layer after the heat treatment.
A PCD insert for a rock-boring drill bit was made as described below.
A pre-sinter assembly was prepared, comprising a PCD structure having a generally disc-like shape disposed against a proximate end of a generally cylindrical cemented carbide substrate. PCD structure had been made in a previous step involving sintering together an aggregation of a plurality of diamond grains at an ultra-high pressure of less than about 7 gigapascals and a high temperature (at which the diamond was thermodynamically more stable than graphite). The substrate comprised about 90 weight percent WC grains cemented together by a binder material comprising Co. The pre-sinter assembly was enclosed in a metal jacket and heated to burn off the organic binder comprised in the wafers, and the jacketed, pre-sinter assembly was encapsulated in a capsule for an ultra-high pressure, high temperature multi-anvil press apparatus.
The pre-sinter assembly was subjected to a pressure of about 7.7 gigapascals and a temperature of about 1,550 degrees Celsius to modify the microstructure of the PCD structure. The pressure was reduced to about 5.5 gigapascals and the temperature was reduced to about 1,450 degrees Celsius, maintaining conditions at which the diamond comprised in the PCD is thermodynamically stable (in relation to graphite, a softer allotrope of carbon) and at which the binder material is in the liquid phase. The temperature was then reduced to about 1,000 degrees Celsius to solidify the binder material and form a construction comprising the layer of PCD bonded to the substrate by the solidified binder material, and the pressure and temperature were then reduced to ambient conditions.
The construction was subjected to a heat treatment at 660 degrees Celsius for about 2 hours at substantially ambient pressure in a substantially non-oxidising atmosphere, and then cooled to ambient temperature. No cracks were evident in the PCD layer after the heat treatment.
The construction was processed by grinding and polishing to provide an insert for a rock-boring drill bit.
Certain terms and concepts as used herein will be briefly explained.
As used herein, “super-hard” means a Vickers hardness of at least 25 gigapascal. Synthetic and natural diamond, polycrystalline diamond (PCD), cubic boron nitride (cBN) and polycrystalline cBN (PCBN) material are examples of super-hard materials. Synthetic diamond, which is also called man-made diamond, is diamond material that has been manufactured.
As used herein, PCBN material comprises grains of cubic boron nitride (cBN) dispersed within a matrix comprising metal and or ceramic material.
PCD material comprises a mass (an aggregation of a plurality) of diamond grains, a substantial portion of which are directly inter-bonded with each other and in which the content of diamond is at least about 80 volume percent of the material. Interstices between the diamond grains may be at least partly filled with a binder material comprising a catalyst material for synthetic diamond, or they may be substantially empty. Catalyst material (which may also be referred to as solvent/catalyst material, reflecting the understanding that the material may perform a catalytic and or solvent function in promoting the growth of diamond grains and the sintering of diamond grains) for synthetic diamond is capable of promoting the growth of synthetic diamond grains and or the direct inter-growth of synthetic or natural diamond grains at a temperature and pressure at which synthetic or natural diamond is thermodynamically more stable than graphite. Examples of catalyst materials for diamond are Fe, Ni, Co and Mn, and certain alloys including these. Bodies comprising PCD material may comprise at least a region from which catalyst material has been removed from the interstices, leaving interstitial voids between the diamond grains. Various grades of PCD material may be made. As used herein, a PCD grade is a variant of PCD material characterised in terms of the volume content and size of diamond grains, the volume content of interstitial regions between the diamond grains and composition of material that may be present within the interstitial regions. Different PCD grades may have different microstructure and different mechanical properties, such as elastic (or Young's) modulus E, modulus of elasticity, transverse rupture strength (TRS), toughness (such as so-called K1C toughness), hardness, density and coefficient of thermal expansion (CTE). Different PCD grades may also perform differently in use. For example, the wear rate and fracture resistance of different PCD grades may be different.
Thermally stable PCD material comprises at least a part or volume of which exhibits no substantial structural degradation or deterioration of hardness or abrasion resistance after exposure to a temperature above about 400 degrees Celsius, or even above about 700 degrees Celsius. For example, PCD material containing less than about 2 weight percent of catalyst metal for diamond such as Co, Fe, Ni, Mn in catalytically active form (e.g. in elemental form) may be thermally stable. PCD material that is substantially free of catalyst material in catalytically active form is an example of thermally stable PCD. PCD material in which the interstices are substantially voids or at least partly filled with ceramic material such as SiC or salt material such as carbonate compounds may be thermally stable, for example. PCD structures having at least a significant region from which catalyst material for diamond has been depleted, or in which catalyst material is in a form that is relatively less active as a catalyst, may be described as thermally stable PCD.
Other examples of superhard materials include certain composite materials comprising diamond or cBN grains held together by a matrix comprising ceramic material, such as silicon carbide (SiC), or cemented carbide material, such as Co-bonded WC material (for example, as described in U.S. Pat. No. 5,453,105 or 6,919,040). For example, certain SiC-bonded diamond materials may comprise at least about 30 volume percent diamond grains dispersed in a SiC matrix (which may contain a minor amount of Si in a form other than SiC). Examples of SiC-bonded diamond materials are described in U.S. Pat. Nos. 7,008,672; 6,709,747; 6,179,886; 6,447,852; and International Application publication number WO2009/013713).
Young's modulus is a type of elastic modulus and is a measure of the uni-axial strain in response to a uni-axial stress, within the range of stress for which the material behaves elastically. A method of measuring the Young's modulus E is by means of measuring the transverse and longitudinal components of the speed of sound through the material using ultrasonic waves.
Various grades of PCD material may be made. As used herein, a PCD grade is a variant of PCD material characterised in terms of the volume content and size of diamond grains, the volume content of interstitial regions between the diamond grains and composition of material that may be present within the interstitial regions. Different PCD grades may have different microstructure and different mechanical properties, such as elastic (or Young's) modulus E, modulus of elasticity, transverse rupture strength (TRS), toughness (such as so-called K1C toughness), hardness, density and coefficient of thermal expansion (CTE). Different PCD grades may also perform differently in use. For example, the wear rate and fracture resistance of different PCD grades may be different.
The ultrahard particles used in the present process may be of natural or synthetic origin. The mixture of ultrahard particles may be multimodal, that it is may comprise a mixture of fractions of diamond particles or grains that differ from one another discernibly in their average particle size. Typically the number of fractions may be:
By “average particle/grain size” it is meant that the individual particles/grains have a range of sizes with the mean particle/grain size representing the “average”. Hence the major amount of the particles/grains will be close to the average size, although there will be a limited number of particles/grains above and below the specified size. The peak in the distribution of the particles will therefore be at the specified size. The size distribution for each ultrahard particle/grain size fraction is typically itself monomodal, but may in certain circumstances be multimodal. In the sintered compact, the term “average particle grain size” is to be interpreted in a similar manner.
As shown in
During the high pressure, high temperature treatment, the catalyst/solvent material melts and migrates through the compact layer, acting as a catalyst/solvent and causing the ultrahard particles to bond to one another. Once manufactured, the PCD construction therefore comprises a coherent matrix of ultrahard (diamond) particles bonded to one another, thereby forming an ultrahard polycrystalline composite material with many interstices or pools containing binder material as described above. In essence, the final PCD construction therefore comprises a two-phase composite, where the ultrahard abrasive diamond material comprises one phase and the binder (non-diamond phase), the other.
In one form, the ultrahard phase, which is typically diamond, constitutes between 80% and 95% by volume and the solvent/catalyst material the other 5% to 20%.
The relative distribution of the binder phase, and the number of voids or pools filled with this phase, is largely defined by the size and shape of the diamond grains.
The binder (non-diamond) phase can help to improve the impact resistance of the more brittle abrasive phase, but as the binder phase typically represents a far weaker and less abrasion resistant fraction of the structure, high quantities will tend to adversely affect wear resistance. Additionally, where the binder phase is also an active solvent/catalyst material, its increased presence in the structure can compromise the thermal stability of the compact.
a and 10b are schematic examples of a processed SEM image of a polished section of a PCD material, shown in negative, for a diamond intensity of 0 (
As a non-limiting example, the cross section shown in
The magnification selected for the microstructural analysis has a significant effect on the accuracy of the data obtained. Imaging at lower magnifications offers an opportunity to sample, representatively, larger particles or features in a microstructure but may tend to under-represent smaller particles or features as they are not necessarily sufficiently resolved at that magnification. By contrast, higher magnifications allow resolution and hence detailed measurement of fine-scale features but can tend to sample larger features such that they intersect the boundaries of the images and hence are not adequately measured. It has been appreciated that it is therefore important to select an appropriate magnification for any quantitative microstructural analysis technique. The appropriateness is therefore determined by the size of the features that are being characterised. The magnifications selected for the various measurements described herein are discussed in more detail below.
Unless otherwise stated herein, dimensions of total binder area, nearest neighbour distance and individual binder area within the body of PCD material refer to the dimensions as measured on a surface of, or a section through, a body comprising PCD material and no stereographic correction has been applied. For example, the measurements are made by means of image analysis carried out on a polished surface, and a Saltykov correction has not been applied in the data stated herein.
In measuring the average or mean value of a quantity or other statistical parameter measured by means of image analysis, several images of different parts of a surface or section (hereinafter referred to as samples) are used to enhance the reliability and accuracy of the statistics. The number of images used to measure a given quantity or parameter may be, for example between 10 to 30. If the analysed sample is uniform, which is the case for PCD, depending on magnification, 10 to 20 images may be considered to represent that sample sufficiently well.
The resolution of the images needs to be sufficiently high for the inter-grain and inter-phase boundaries to be clearly made out and, for the measurements stated herein an image area of 1280 by 960 pixels was used.
In the statistical analysis, 15 images were taken of different areas on a surface of a body comprising the PCD material, and statistical analysis was carried out on each image.
Images used for the image analysis were obtained by means of scanning electron micrographs (SEM) taken using a backscattered electron signal. The back-scatter mode was chosen so as to provide high contrast based on different atomic numbers and to reduce sensitivity to surface damage (as compared with the secondary electron imaging mode).
A number of factors have been identified as being important for image capturing. These are:
Given the above conditions, the image analysis software used was able to separate distinguishably the diamond and binder phases and the back-scatter images were taken at approximately 45° to the edge of the samples.
The magnification used in the image analysis should be selected in such a way that the feature of interest is adequately resolved and described by the available number of pixels. In PCD image analysis various features of different size and distribution are measured simultaneously and it is not practical to use a separate magnification for each feature of interest.
It is difficult to identify the optimum magnification for each feature measurement in the absence of a reference measurement result. It could vary from one operator to another. Therefore, a procedure is proposed for the selection of the magnification.
The size of a statistically significant number of diamond grains in the microstructure is measured and the average value taken.
As used herein in relation to grains or particles and unless otherwise stated or implied, the term “size” refers to the length of the grain viewed from the side or in cross section using image analysis techniques.
The number of pixels that describe this average length is determined and a range of pixel values are established to fix the magnification.
In the image analysis technique, the original image was converted to a greyscale image. The image contrast level was set by ensuring the diamond peak intensity in the grey scale histogram image occurred between 15 and 20.
As mentioned above, several images of different parts of a surface or section were taken to enhance the reliability and accuracy of the statistics. For measurements of total binder area, the greater the number of images, the more accurate the results are perceived to be. For example, about 15000 measurements were taken, 1000 per image with 15 images.
The steps taken by the image analysis programme may be summarised in general as follows:
If appropriate thresholding is used, the image analysis technique is unlikely to introduce further errors in measurements which would have a practical effect on the accuracy of those measurements, with the exception of small errors related to the rounding of numbers. In the current analysis, the statistical mean values of the total binder area and individual binder areas were used as, according to the Central Limitation Theorem, the distribution of an average tends to be normal as the sample size increases, regardless of the distribution from which the average is taken except when the moments of the parent distribution do not exist. All practical distributions in statistical engineering have defined moments, and thus the Central Limitation Theorem applies in the present case. It was therefore deemed appropriate to use the statistical mean values.
The individual non-diamond (eg binder or catalyst/solvent) phase areas or pools, which are easily distinguishable from that of the ultrahard phase using electron microscopy, were identified using the above-mentioned standard image analysis tools. The total non-diamond phase areas (in square microns) in the analysed cross-sectional images were determined by summing the individual binder pool areas within the entire microstructural image area that was analysed, as were the distances between nearest neighbouring grains/particles of the non-diamond phase.
The collected distributions of this data were then evaluated statistically and an arithmetic average was then determined for each property being considered. Hence the mean total binder pool area in the surface of the microstructure being analysed was calculated as was the average of nearest neighbour distances between non-diamond phase grains/particles.
It is anticipated that microstructural parameters may alter slightly from one area of an abrasive compact to another, depending on formation conditions. Hence the microstructural imaging is carried out so as to representatively sample the bulk of the ultrahard composite portion of the compact.
Non-limiting examples are now described. Three sets of samples were produced as follows: a multimodal (trimodal) diamond powder mix with average diamond grain size of approximately 13 μm and 1 weight percent cobalt admix was prepared, in sufficient quantity to provide approximately 2 g admix per sample. The admix for each sample was then poured into or otherwise arranged in a Niobium inner cup. A cemented carbide substrate of approximately 13 weight percent cobalt content and having a non-planar interface was placed in each inner cup on the powder mix. A titanium cup was placed in turn over this structure and the assembly sealed to produce a canister. The canisters were pre-treated by vacuum outgassing at approximately 1050° C., and divided into three sets which were sintered at three distinct ultrahigh pressure and temperature conditions in the diamond-stable region, namely at approximately 5.5 GPa (Set 1), 6.8 GPa (Set 2), and 7.7 GPa (Set 3). Specifically the canisters were sintered at temperatures sufficient to melt the cobalt so as to produce PCD constructions with well-sintered PCD tables and well-bonded substrates. The technique described above in connection with
Image analysis was then conducted on each of these superhard constructions using the techniques described above and in particular the determination of appropriate magnification described above to determine the mean total binder area in a polished cross-section, the mean cross-sectional binder area for each sample and the average nearest neighbour distance between non-diamond phase particles/grains.
The experiments may be repeated for different diamond grain size compositions and the results for mean total binder area in a polished cross-section and the mean cross-sectional binder area for each sample are set out in Table 1.
Whilst wishing not to be bound by theory, it is believed that the above described method steps enable the formation of polycrystalline diamond constructions in which it was determined from the above experiments that, for a total non-diamond phase area (for example binder area) in the range of around 0 to 5%, it is possible to achieve an average nearest neighbour distance between the particles/grains of the non-diamond phase of less than around 1.3 microns. It was also determined that, for a total non-diamond phase area (for example binder area) in the range of around 0 to 5%, it is possible to achieve an associated individual non-diamond area of less than 0.7 micron2. These values were determined using an image analysis technique applying a magnification of around 1000 and analysing an image area of 1280×960 pixels, with the largest dimension of the body of PCD material being around 6 mm or greater. The thickness of the body of PCD material in these embodiments may be, for example, around 0.3 mm or greater.
Furthermore, for a total non-diamond phase area (for example binder area) in the range of around 5 to 10%, it is possible to achieve an average nearest neighbour distance between the particles/grains of the non-diamond phase of less than around 1.04 microns. It was also determined that, for a total non-diamond phase area (for example binder area) in the range of around 5 to 10%, it is possible to achieve an associated cross-sectional individual non-diamond phase area of less than 0.340 micron2. These values were determined using an image analysis technique applying a magnification of around 1000 and analysing an image area of 1280×960 pixels, with the largest dimension of the body of PCD material being around 6 mm or greater. The thickness of the body of PCD material in these embodiments may be, for example, around 0.3 mm or greater.
Also, for a total non-diamond phase area (for example binder area) in the range of around 10 to 15%, it is possible to achieve an average nearest neighbour distance between the particles/grains of the non-diamond phase of less than around 1.04 microns. It was also determined that, for a total non-diamond phase area (for example binder area) in the range of between around 10 to 15%, it is possible to achieve an associated cross-sectional individual non-diamond phase area of less than 0.340 micron2. These values were determined using an image analysis technique applying a magnification of around 3000 and analysing an image area of 1280×960 pixels, with the largest dimension of the body of PCD material being around 6 mm or greater. The thickness of the body of PCD material in these embodiments may be, for example, around 0.3 mm or greater.
For a total non-diamond phase area (for example binder area) in the range of around 15 to 30%, it is possible to achieve an average nearest neighbour distance between the particles/grains of the non-diamond phase of less than around 0.8 microns. It was also determined that, for a total non-diamond phase area (for example binder area) in the range of between around 15 to 30%, it is possible to achieve an associated cross-sectional individual non-diamond phase area in the range 0.005 to 0.340 micron2. These values were determined using an image analysis technique applying a magnification of around 10000 and analysing an image area of 1280×960 pixels, with the largest dimension of the body of PCD material being around 6 mm or greater.
The thickness of the body of PCD material in these embodiments may be, for example, around 0.3 mm or greater.
Whilst not wishing to be bound by a particular theory, using the conditions described herein it was determined possible to achieve an average nearest neighbour distance between the particles/grains of the non-diamond phase and total binder areas in the ranges specified above together with the above-mentioned ranges of associated individual binder areas. It is believed these may assist in generating a more wear-resistant body of PCD material which, when used as a cutter, may significantly enhance the durability of the cutter produced according to some embodiments described herein.
In addition, various arrangements and combinations are envisaged for the method by the disclosure, and examples of the method may further include one or more of the following non-exhaustive and non-limiting aspects in various combinations.
There may be provided a method for making a super-hard construction comprising:
In some embodiments, the CTE of one of the first or second materials is at least about 2.5×10−6 per degree Celsius and at most about 5.0×10−6 per degree Celsius and the CTE of the other of the first or second materials is at least about 3.5×10−6 per degree Celsius and at most about 6.5×10−6 per degree Celsius, at about 25 degrees Celsius.
In some embodiments, the Young's modulus of one of the first or second materials is at least about 500 gigapascals and at most about 1,300 gigapascals and the Young's modulus of the other of the first and second materials is at least about 800 gigapascals and at most about 1,600 gigapascals.
In some embodiments, the Young's moduli of the first and second materials differ by at least about 10% and in some embodiments, the CTE of the first and second materials may differ by at least about 10%.
The method may include sintering an aggregation of a plurality of grains of the super-hard material in the presence of sinter catalyst material at a sinter pressure and a sinter temperature to form the second structure.
In some embodiments, the method may include disposing an aggregation of grains of super-hard material adjacent the first structure and in the presence of the binder material to form a pre-sinter assembly; subjecting the pre-sinter assembly to a sinter pressure and a sinter temperature to melt the binder material and sinter the grains of super-hard materials and form the second structure comprising polycrystalline super-hard material connected to the first structure by the binder material in the molten state.
In some embodiments, the first pressure is substantially the sinter pressure.
The method may include providing the first structure, providing the second structure comprising polycrystalline super-hard material, disposing the first structure adjacent the second structure and forming a pre-construction assembly, and applying a pressure to the pre-construction assembly, increasing the pressure from ambient pressure to the first pressure.
In some embodiments, the method may include subjecting an aggregation of a plurality of grains of super-hard material to a sinter pressure and a sinter temperature at which the super-hard material is capable of being sintered to form the second material, and reducing the pressure and temperature to an ambient condition to provide the second structure; the first pressure being substantially greater then the sinter pressure.
The second structure may, for example, comprise diamond material and the binder material comprises catalyst material for diamond. In some embodiments, the first and second structures each comprise diamond material and the binder material comprises catalyst material for diamond.
In some embodiments, the difference between the second pressure and the first pressure is at least about 0.5 gigapascal.
The method may include subjecting the super-hard construction to further heat treatment at a treatment temperature and a treatment pressure at which the super-hard material is thermodynamically meta-stable.
In some embodiments, the super-hard material comprises diamond material and the treatment temperature is at least about 500 degrees Celsius and the treatment pressure is less than about 1 gigapascal.
The method may include reducing the pressure from the first pressure to an intermediate pressure for a holding period, and then further reducing the pressure from the intermediate pressure to the second pressure.
In some embodiments, the first pressure is at least about 7 gigapascal, the intermediate pressure is at least about 5.5 gigapascals and less than about 10 gigapascals, the holding period is at least about 1 minute and the second pressure is at least about 5.5 gigapascals and at most about 7 gigapascals.
The method may include processing the super-hard construction to provide a tool element.
In some embodiments, the super-hard construction is configured for a tool element for a rock-boring drill bit. In other embodiments, the super-hard construction is configured for an impact tool for degrading rock or pavement.
In some embodiments, the pressure at which the binder material begins to solidify responsive to the reduction in temperature is substantially equal to the second pressure.
In some embodiments, the pressure at which the binder material begins to solidify responsive to the reduction in temperature is substantially less than the second pressure.
In some embodiments, the first structure comprises cobalt-cemented tungsten carbide material and the second material comprises PCD material, the CTE of the cemented carbide material being in the range of about 4.5×10−6 to about 6.5×10−6 per degree Celsius, the CTE of the PCD material being in the range of about 3.0×10−6 to about 5.0×10−6 per degree Celsius; the Young's modulus of the cemented carbide material being in the range of about 500 to about 1,000 gigapascals, and the Young's modulus of the PCD material being in the range of about 800 to about 1,600 gigapascals; the first pressure being in the range of about 6 to about 10 gigapascals, and the second pressure being in the range of about 5.5 to about 8 gigapascals.
The pressure at which the cobalt-based binder material comprised in the cemented carbide material begins to solidify may, in some embodiments, be equal to the second pressure.
In some embodiments, the second pressure is in the range of about 6.5 to about 7.5 gigapascals.
In some embodiments, the second structure comprises PCD material and the method includes subjecting the super-hard construction to further heat treatment for a treatment period in the range of about 30 to about 90 minutes at a treatment temperature in the range of about 550 to about 650 degrees Celsius.
Disclosed methods have the aspect of reducing the likelihood or frequency of cracking of super-hard constructions, particularly when subjected to heating in subsequent manufacturing steps or to elevated temperatures in use.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1118776.2 | Oct 2011 | GB | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2012/071295 | 10/26/2012 | WO | 00 | 4/28/2014 |
| Number | Date | Country | |
|---|---|---|---|
| 61553646 | Oct 2011 | US |
