IE65120B1 - Coated superabrasive grit and use of same - Google Patents

Description

COATED SUPERABRASIVE GRIT AND USE OF SAME The present invention relates to a coated superabrasive grit which is useful for producing improved abrasive or cutting tools. The present invention also includes within its scope the tools thus produced embodying the coated grit.

Superabrasives grit such as diamond and CBN, attached to a supporting body, is widely used for removing materials. Typical applications include, for example, sawing, drilling, dressing, grinding, lapping and poli shing.

In typical applications, the grit is held in a suitable matrix and attached to a tool body. The retention of the grit is primarily accomplished by mechanical means, such as by surrounding the grit with the matrix material. This method of attachment, although simple and practical, has limitations because the exposure of the grit must be limited so as not to weaken the mechanical grip of the surrounding matrix. As a result, the cutting rate is limited by the small grit exposure. Further, as the matrix is worn down, the retention becomes insufficient so the grit can be pulled out and lost. For example, in a typical saw blade application, the average exposure of the diamond grit is less than 20% of the total grit height, and the grit is often lost due to the pull-out when it is worn down to about 1/3 of its original size. After using this saw blade for some time, typically about 1/3 of the original grit is lost as evidenced by the empty pockets on the blade. 651 20 - 2 In order to overcome this problem, a coating of grit has been attempted to improve the bonding strength. U.S. Patent No. 3,650,714 to Farkas describes a process for applying such coating on a diamond grit. Typical commercially available coated superabrasives products include DeBeer Co.'s titanized products for saw grit and General Electric Co.'s titanized products for CBN grit. For all metal matrix superabrasives tools the only commercially available coating for grit is titanized products.

However, it has been found that titanized products, particularly for diamond grit, are not effective in improving the attachment strength. The performance evaluation i.e. life and cutting rate of titanized grit in saw blade applications did not show noticeable improvements. One problem encountered by the titanized product is its lack of resistance against oxidation. It is well known that Ti or TiC can be oxidized in most saw blade manufacturing conditions. The oxidation can destroy the bonding between the grit and coating material, and between the coating material and the matrix. The other problem titanized products faced is the thinness of the coating. Titanized products typically contain less than 1 yum thick of Ti or TiC. Such a thin coating can not prevent the dissolution or removal of the coating from the grit surface by the matrix material during the manufacturing process for tools. U.S. Patents 3,757,878 and 3,757,879 to Wilder describe an encapsulation method for diamond particles. However, this is directed to produce a mechanical envelope for the grit and no chemical bonding is achieved.

In Patent Abstract of Japan, Vol. 13, No. 331, an alloy-coated superabrasive grain is disclosed which consists of diamond or boron nitride and which is coated with a Ni-W alloy.

The grain is used to obtain a whetstone of long working life.

The invention. solves the above problem by providing the coated superabrasive grit according to independent claim 1 and a process of independent claim 9. The invention further provides a tool making use of the grit according to independent claim 7 and a cutting tool making use of this grit according to independent claim 13. Further advantageous objects, aspects and features of the invention are evident from the dependent claims, the description and the examples.

According to a further aspect, the invention provides a coated superabrasvie grit comprising superabrasive grit particles, a carbide former coating which is relatively oxidation resistant, said coating being substantially continuous on the grit with a thickness of at least 1 yum and being chemically bonded thereto. Advantageously, this grit coating is a member selected from the group consisting of W, Mo, Ta, Nb and alloys thereof and/or tungsten. According to a further aspect this grit is a member selected from the group consisting of diamond and CBN. The aforementioned grit may include a second coating over said coating. According to a further aspect the surface of the aforementioned superabrasive grit particles is roughened.

This invention provides a chemically coated superabrasive grit.

This invention further achieves a firm attachment of the grit in the matrix body of a tool.

This invention also provides a continuous thick coating of at least 1 ^um on the superabrasives grit so the integrity of coating can be maintained after tool manufacturing process.

According to another aspect, this invention provides a coating material which is substantially inert to oxidation during tool manufacturing processes.

Yet another aspect is to provide abrasive or cutting tools embodying such chemically bonded coating superabrasive for imciroved material removal performance.

A further aspect is to provide tools with the chemically coated abrasive grit exhibiting better grit retention, larger grit protrusion, and freer cutting action. These tools include, for example saw blades, grinding wheels, dressing tools, drill bits, and lappina tools.

The term superabrasive used in tte fecripticn end in the claims means natural, as well as synthetic diamond and cubic boron nitride (CBN).' The term “chemical bonding as used herein is distinguishable from mechanical bonding. In the latter case, there is no reaction between the two joining members.

In the case of chemical bonding, there is a reaction on the interface between the two joining members. The reaction may be, for example, a carbide formation, a boride formation, a nitride formation, or a solution formed by inter-diffusion between the two joining members.

The teem drill bit used hereinafter and in the claims comtemplates not only machine tool type drill bits but also includes drill bits and core bits such as those commonly employed in the mining and petroleum industry for earth boring.

According to the present invention, there is provided a superabrasive grit which is coated with a relatively non-oxidizable metal of at least one μη thickness that is strongly bonded to the surface of the grit by a chemical bond. Briefly, the grit is coated with a metal which is not readily oxidizable selected from W, Ta, « Mo, Nb or alloys thereof. The coated grit is then thermally treated either before or during the manufacturing process for tools to form a strong chemical bond between the coating* - 5 and the grit such as a carbide layer in the case or a diamond grit. Tungsten is the preferred metal for the coating. The surface of the grit can optionally be roughened by either chemical or mechanical means before being coated to enhance subsequent bcncing. The composition of the matrix must be compatible with the coating materials selected for the grit so that under the processing conditions for tool manufacturing, the matrix will be chemically bonded to the coating material. The result, is a firmly attached chemically bonded coated superabrasive grit in a tool matrix.

The interfaces between the superabrasive grit and the coating, and between the coating and the matrix are formed by strong chemical bonds. This is distinguished from prior art practices where the attachment of grit is primarily achieved mechanically by the surrounding matrix material. The coated superabrasive grit when embodied in a tool in accordance with this invention has the following advantage s: 1. longer life due to less grit pull-outs; 2. higher cutting rate due to larger grit protrusion; and 3. freer cutting with lower force, lower power, less heat generation due to larger grit protrusion .

The coated superabrasive according to this invention is particularly suitable for grit in drill bits such as, for example, a sub-component of a cutter having a particular physical form such as circle, oval, blade anc the like; or as an actual cutting component itself, as when the grit is incorporated in the actual matrix of the bic protruding from the surface thereof, wearing away, and exposing other pieces of grit bonded to the matrix. This is particularly suitable for core bits, although other bits for hard formations can be similarly manufactured. g rit Accord surface is ing to this invention, the superabrasives first roughened by mechanical or chemical - 6 means. The roughening produces ar. uneven surface which improves the adherence of the grit to the coating material to be applied later. This improvement of aaherence is the result of increased chemical reactivity of the grit surfaces due to much higher amount of surface imperfections. The number of unbonded electrons of carbon on the surface will also increase, thereby enhancing the reaction between the grit and the coating material. The unevenness of the surface can also strengthen the mechanical attachment of the grit to the coating material due to the larger surface area of close contact.

In the practice of this invention, the grits are optionally roughened at first. A preferred roughening is to form a uniformly distributed frosted surface. This roughening is accomplished by either mechanical means, such as by milling with other superabrasive powders, or chemical means such as by oxidation or etching. For example, a grit can be tumbled in air or enriched oxygen atmosphere at high temperature to allow even oxidation on all surfaces. A fluidized bed chemical vapor deposition (CVD) system or a rotary furnace can both be advantageously employed to produce the desired results. For chemical etching processes, oxidants such as potassium dichromate or potassium nitrate may be optionally used. Employing either method, the weight loss of the grit during the surface roughening treatment should be controlled to be less than 5% w/w.

Although the surface roughening is an important step according to this invention, it may not be necessary for some applications. For example, for smaller sized grit applications, such as for polishing cloths using micron powders, the roughening step may be eliminated.

After the surface roughening treatment, the grit is washed and chemically cleaned to remove surface contaminants by methods known in the art. For example, washing the grit in mineral acids such as with a solution of nitric or hydrochloric acid, or heating the grit under hydrogen atmosphere can eliminate most surface contaminants. least 1 pm pm pm. to about 50 pm to about 30 pm.

After surface cleaning, the grit is coated with a material which is relatively oxidation resistant, and which is a carbide former such as W, Ta, Mo, and Nb, or an alloy thereof forming a continuous layer having a thickness of at The coating thickness can vary from aoout 1 and preferably from about 1 Such a coating is readily distinguishable from coatings known in the art. See for example, the coating obtained in accordance with the description in Farkas U.S. Patent 3,650,714 which is much thinner than 1 pm. This distinction is also applicable for other commercially available titanized products.

In the case where diamond grit is used, a carbide is formed between the grit and the coating material by heating the coated grit to carbide forming temperatures. Where CBN is used a nitride bond is formed. As a suitable alloy coating there may be mentioned for example, W-Ni3.

After the first coating material is applied to the grit, a second coating or any additional layers of coating can be optionally applied over the first layer. The purpose of the multi-layers is to provide additional protection of the first coating layer from oxidation in the air or from dissolution into the matrix material during the manufacturing process of the tool, and/or during the cutting action of the tool. The outer coating can also provide a better metallurgical joint with the matrix bond material so as to form a diffusion bonded interface. For most applications, the outer coating layer need not contain a carbide former. For example, an electroless outer coating of copper can be used to bond with certain matrix materials .

The coating is typically applied by known methods such as chemical vapor deposition described by Wilder in U.S. Patent 3,757,878. These methods are used to apply these mechanical layers which do not normally contain oxidation resistant carbide formers.

The chemical bonding between the grit and the coating is achieved by a way depending upon the desired final product. Thus for example, if the grit is to be embodied in a saw blade, the processing conditions to form the blade, especially the temperature required to form the blade, will be sufficient to cause the formation of the chemical bonding. On the other hand, if the desired end product is formed at different process conditions which will not induce sufficient chemically bonding, the coated grit is pre-treated under conditions such as in a furnace for example at an effective carbide forming temperature such as about 850°C to cause the formation chemical bonding before using the grit in the end product.

After the coating is applied to the grit, the coated grit can be used like an uncoated one for the subsequent processing for making tools. In the case of making a saw blade for example, the grit is mixed with a well blended matrix metal powder and then either hot pressed at about 800°C to 1000°C to shape, or infiltrated with a binder alloy. The result is a saw blade with grit chemically bonded by the coating material and coating material chemically bonded to the matrix material. Simply put, all the interfaces are joined by chemical bonds.

In another embodiment of this invention, the coated grit is packed to form a very high density mass. For example, by means of vibrational packing, monosized grit (500 pm in size) can reach a packing efficiency of about 55% (the rest, 45%, is porosity). By adding a second sized grit (70 pm .), which is about 1/7 of the first sized grit, the packing efficiency can be increased to about 77%.

A further addition of the third sized grit which is again about 1/7 in size of the second one, the whole mass can achieve a packing efficiency of over 83%. After the grit is packed, the mass is infiltrated by an alloy which has a melting point below the degradation temperature of the superabrasives grit. If a diamond grit is used, the temperature limit is less than about 1100°C for synthetic - 9 grit depending on quality, and for about 1300°C for nacural grit. Because of the presence of the coating, the binder alloy infiltrates the highly packed mass of superabrasives grit relatively easily. Without the coating, most binder alloys can not infiltrate such a mass.

Following this embodiment we obtain a superabrasive-metal composite material, such as diamond-metal composite which we call Diamet. This composite material possesses higher impact resistance than a typical polycrystalline superabrasives aggregate because of the presence of the metal binder. For example, we have obtained a Diamet mass which is tougher than a polycrystalline diamond (PCD) ma'terial when these products are subjected to impact testing.

The Diamet material is readily bondable onto a cemented WC substrate to form, for example, cutters useful for drill bits for earth boring applications. Such cutters with backing have been tested in a laboratory and the cutting results are comparable to those cutters made of compacts such as Geoset.

The method, according to this invention, offers many advantages. For example, it does not involve using very high pressure which is required for making a polycrystalline superabrasives aggregate such as a PCD; therefore, the cost for making this composite material can be much less than the prior art methods. The size and shape of this material can also be more flexible without being restricted by the high pressure chamber.

In order to further illustrate the practice of this invention, the following examples are included: EXAMPLE I A natural diamond grit available under the trade name of EMBS supplied by DeBeers Co. with a size (30/40 U.S. mesh) having a F.E.P.A. designation of D602 was coated by a tungsten layer using fluidized bed CVD method. Thus, the diamond grits were dipped in an acid solution comprising -1 0of hydroflouric and nitric acid for about 1 minute. They were rinsed in deionized water for 15 minutes followed by washing in dilute NaOH solution for 2 minutes and a further rinsing in deionized water. The cleaned grits were dried in an oven. The dried diamond grits were loaded in a chemical vapor deposition (CVD) reactor comprising a graphite tube. ( After the diamond grits were loaded in the reactor, argon was introduced into the reaction chamber at a pressure of about 667 Pa (5 torr) for about 30 mins. Thereafter, the pressure was changed to 66.7 Pa (0.5 torr) to allow water to evaporate. Then a gas comprising Ar, He, H2 at 1:1:1 ratio was introduced into the chamber at a pressure of 667 Pa (5 torr) and at a flow rate of 0.21 liter per minute while the reactor was heated up to 900°C in 16 minutes and held at θΟΟ’ϋ for 30 minutes. The temperature was lowered to 700°C in 3 minutes and then the pressure was raised to 1.6 kPa (12 torr). The flow rate of the gas was increased to fluidize the diamond grits in the reactor WF6 simultaneously (tungsten hex fluoride) was introduced to effect the deposition of tungsten on the diamond reaching 11 pm in about 75 minutes. Finally, a flow of argon only was introduced to allow the reactor to cool down to room temperature. The tungsten coating thickness on the product was 7.7 5 pm The coated grit was made into saw segments by hot pressing with a matrix material made of 80% Cu-Sn alloy and 20% cemented tungsten carbide grit. These segments were used to cut an abrasive concrete sample containing chert grains. The results indicated that the pull-out loss of the grit was reduced to less than 10% on the cutting surface after testing. This low pull-out loss is in sharp contrast with 40% from a parallel test using uncoated grit under identical conditions.

EXAMPLE II A synthetic diamond grit available under the trade name SDA100 also supplied by DeSeers Co. with a size having a F.E.P.A. designation of D602 was coated with a tungsten layer of about 10 pm thickness as in Example I. The -11 coated grit was spread out to form a plane of tightly packed monolayer in a matrix powder body made of tungsten carbide The assembly was pre-pressed into shape and later hot pressed at a temperature of 815°C and at a pressure of 24 rtPa (3,500 psi) The hot pressed mass was in a dog-bone shape. The tensile test specimen was then subject to a pulling test (uniaxial tensile test,. The results indicated the coated grit in such a geometry can support a tensile strength of 2.3 kg/cm’ (15 KSI). Uncoated grit under the identical testing condition showed virtually no tensile strength.

The above coated grit was also overcoated by an electroless deposited nickel boron layer of about 30 pm thick by a procedure supplied by Allied-Kelite division of Witco Corp. A solution comprising of nickel-boron, available from Witco Corp., was employed. In the first step of coating, the tungsten surface was cleansed using a solution such as Niklad Alprep 230 solution from Witco by heating the solution to 65.5°C and the diamond grits were dipped in for 5 minutes. Then the diamond grits were rinsed in tap water until the foam was gone. A sensitizer available as Niklad 261, from Witco, was applied to the diamond grit surfaces by dipping the grit's therein at 224eC for 2 minutes. Then the diamond grits were rinsed in deionized water. A catalyst available under the trademark Niklad 262 was then applied to the diamond grit surface by dipping the diamond grits therein at 43°C for 4 minutes at a PH of 1.9 to 3. Then the diamond grits were rinsed in deionized water. The treated diamond grits were dried and dipped in a Ni-B solution available as Niklad 752 solution at a PH of about 6 and at a temperature of 80°C. The nickel layer contained about 3% of boron. Under the same testing condition the tensile strength was 3.1 kg/cm2 (20KSI).

In a parallel test, a same type grit was first roughened on surfaces and then coated by the same double layers. The surface roughening was done by a milling action against diamond micron powders in a water medium. The -1 2milling lasted for 24 hours and the grit had a final weight loss of about 0.7%. Under the above test conditions, the tensile strength was increased to 5.4 kg/cm’ (35 KSI).

EXAMPLE III Tungsten coated diamond micron powders produced by ' the method described in Example I with size of 500 um & pm were packed by vibration to form an uniformly * distributed mass of 80% packing efficiency. The mass was then infiltrated by an alloy composed of copper, manganese and titanium under vacuum at 1050°C for 20 minutes. The Diamet was made into a cutter and used to cut a granite log wi.th coolant. The wear resistance was measured ar.d compared with other commercially available PCD materials tested under the same conditions. The results indicated that the wear resistance of Diamet is comparable to Geoset-type PCD supplied by General Electric Company. The latter product is made under high pressure conditions in diamond stability region. The same Diamet sample was also subject to an erosion test by injecting an abrasive containing mud. The erosion resistance was found to be comparable to infiltrated tungsten carbide slug which is typically used as the -face of a matrix bit body. The Diamet material with such high wear resistance and erosion resistance is useful to form cutters in drill bits for rock drilling. The drill bits known in the art typically used PCD (such as Geoset) or tungsten carbide inserts.

EXAMPLE IV Diamet cutters made according to Example III were brazed into a bit body by a typical brazing procedure known in the art employing a 19.05 cm (8-1/2) bit body.

Claims (15)

Claims:

1. A coated superabrasive grit, which can support a tensile strength of 2.3 kg/cm 2 (15 KSI) comprising superabrasive grit particles, selected from the group consisting of diamond and CBN, said grit particles being surface cleaned and covered with a substantially continuous metal coating selected from the group consisting of W, Mo, Ta, Nb and alloys thereof, said coating having a thickness of 1 gm to 50 gm and being chemically bonded to the grit particles.

2. The coated superabrasive grit of claim 1, further comprising superabrasive grit particles having roughened surfaces.

3. The coated superabrasive grit of any one of the preceding claims, further comprising a second substantially continuous metallic coating on top of said first metallic coating, said second metallic coating comprising nickel or copper, said first and second metallic coatings having a total thickness in the range of about 1 to 50 gm.

4. A coated superabrasive grit as defined in claim 3, wherein said first metallic coating is tungsten.

5. A coated superabrasive grit as defined in claim 3 or 4, wherein said second metallic coating comprises nickel.

6. A coated superabrasive grit as defined in one of claims 2 to 5, wherein said second metallic coating oanprises NiB.

7. A coated superabrasive grit as defined in claims 2 to 6, wherein said first metallic coating is tungsten and said second metallic coating comprises NiB. -1 4g_ A coated superabrasive grit as defined in one of claims 2 to 7, wherein said first metallic coating is about 10 μιη thick and said second metallic coating is about 30 μπι thick.

8. 9. A process for making a coated superabrasive grit comprising superabrasive grit particles selected from the group consisting of diamond and CBN comprising the steps of: surface cleaning the grit which step includes rinsing the grit in deionized water and coating the cleaned grit with a metal which is not readily oxidizable, selected from W, Ta, Mo, Nb or alloys thereof in a thickness of 1 μπι to 50 μπι and thermally treating the coated grit to form a strong chemical bond between the coating and the grit.

9. 10. A tool which comprising a coated superabrasive grit according to one of claims 1 to 8 which is in contact with a matrix and said matrix being bonded to a tool body.

10. 11. A tool according to claim 10, in which the tool body is metallic.

11. 12. A tool according to claim 10, in which the tool body is nonmetallic.

12. 13. A tool according to claim 10 which is a saw blade.

13. 14. A tool according to claim 10 which is a drill bit.

14. 15. A tool according to one of claims 11 to 14 in which the grit has a packing efficiency of more than 70% by volume.

15. 16. 5 17. 18. 1 Ο 19. -1 5A cutting tool which comprises as cutting members, a coated superabrasive grit according to one of claims 1 to 8, and said grit being an integral part of a tool. A coated superabrasive grit according to claim 1 , substantially as herein described. A tool according to claim 10 or claim 16, substantially as herein described. A process for making a coated superabrasive grit according to claim 9, substantially as herein described.