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Title:
A GRINDING TOOL FOR MACHINING BRITTLE MATERIALS AND A METHOD OF MAKING A GRINDING TOOL
Document Type and Number:
WIPO Patent Application WO/2013/015737
Kind Code:
A1
Abstract:
The invention relates to a grinding tool 1 for machining brittle materials. The grinding tool 1 has a core 2 and an abrasive rim 4. The abrasive rim 4 comprises abrasive particles 5 embedded in a matrix 6. The matrix 6 comprises a metallic bonding agent and possibly also a polymeric bonding agent. The metallic bonding agent contains silicon nitride in an amount that constitutes 0.02% -5.0 % by volume of the metallic bonding agent. The invention also relates to a method of manufacturing the grinding tool. In the method, abrasive particles are mixed with metal powder and silicon nitride and the mixture is sintered. Polymeric powder may also be added before sintering.

Inventors:
THOLIN MICHAEL (SE)
WESTBERG FREDRIK (SE)
BERGH STEFAN (SE)
JOHANSSON IDA (SE)
Application Number:
PCT/SE2012/050842
Publication Date:
January 31, 2013
Filing Date:
July 18, 2012
Export Citation:
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Assignee:
SLIPNAXOS AKTIEBOLAG (SE)
THOLIN MICHAEL (SE)
WESTBERG FREDRIK (SE)
BERGH STEFAN (SE)
JOHANSSON IDA (SE)
International Classes:
B24D3/34; B22F1/18; B22F3/16; B22F7/06; B24D3/06
Foreign References:
JP2002001668A2002-01-08
JP2009241157A2009-10-22
US6063148A2000-05-16
JPS61100374A1986-05-19
Other References:
E. D. KIZIKOV ET AL.: "Microadditions to alloys of the system Cu-Sn-Ti, Institute of Superhard Materials, Academy of Science of the Ukrainian SSR, Kiev", TRANSLATED FROM METALLOVEDENIE I TERMICHESKAYA OBRABOTKA METALLOV, no. 1, January 1987 (1987-01-01), pages 50 - 53, XP055141240
See also references of EP 2734334A4
Attorney, Agent or Firm:
HYNELL PATENTTJÄNST AB (Hagfors, SE)
Download PDF:
Claims:
CLAIMS

1. A grinding tool (1) for machining hard and/or brittle materials whicl grinding tool (1) comprises a core (2) and an abrasive rim (4), the abrasive rim (4 comprising abrasive particles (5) embedded in a matrix (6), the matrix (6) compri metallic bonding agent which is a sintered bronze alloy, the metallic bonding agei constituting 50 % - 100 % by volume of the matrix, the metallic bonding agent containing silicon nitride in an amount that constitutes 0.02 % - 5.0 % by volume metallic bonding agent characterized in that the silicon nitride is present in the sh< grains having an average grain size which is less than ΙΟμιη and above 0. Ι μπι. 2. A grinding tool (1) according to claim 1, wherein the matrix (6) furt comprises a polymeric bonding agent that has been sintered together with the met bonding agent such that the polymeric bonding agent and the metallic bonding ag form a connected network.

3. A grinding tool (1) according to claim 1 or claim 2, wherein the sili< nitride constitutes 0.3 % - 5.0 % by volume of the metallic bonding agent, prefera

0.5 % - 3 % by volume and even more preferred 0.5 % - 2 % by volume.

4. A grinding tool according to claim 2, wherein the polymeric bondin agent comprises polyimide.

5. A grinding tool according to claim 1 or claim 2, wherein the matrix additionally comprises filler materials such as graphite.

6. A grinding tool according to any of claims 1 - 5, wherein the metall bonding agent is a bronze alloy that comprises copper, tin and silver.

7. A grinding tool according to any of claims 1 - 6, wherein the abrasi particles (5) are diamond particles or cubic boron nitride particles. 8. A grinding tool according to claim 7, wherein the abrasive particles have a mean particle size in the range of 4μπι - 181 μπι and preferably in the rang( 46μπι - 91 μπι.

9. A grinding tool according to claim 8, wherein the abrasive particles have a coating of copper or nickel. 10. A method of making a grinding tool (1) which method comprises sii abrasive particles together with metallic powder that comprises copper and tin su< the sintering results in a matrix (6) in which the abrasive narticles (6) are embedd matrix comprising a metallic bonding agent which is a sintered bronze alloy, characterized in that silicon nitride in the form of a powder is added to the metalli powder before sintering and to such an extent that the silicon nitride will constitui % - 5.0% by volume of the metallic bonding agent and wherein the silicon nitride is added is in the shape of grains having an average grain size which is less than 1 and above 0.1 μιη.

11. A method according to claim 10, wherein the metallic powder addit comprises silver.

12. A method according to claim 10 or claim 11, wherein a polymer is to the metallic powder before sintering, preferably in the form of polyimide powd such that also a polymeric bonding agent is formed which is a part of the matrix (

13. A method according to any of claims 10 - 12, wherein the method comprises; mixing the powder material for the bonding agents of the matrix (6) w abrasive particles (5); compacting the mixture in a cold press; curing the compact mixture in a kiln at a temperature in the range of 380°C - 520°C, preferably 400°( 500°C, for a period of 120 - 150 minutes; thereafter placing the compacted and ci mixture in a press and subjecting it to a pressure of 1500 - 2000 kg/cm2; and hole the pressure until the mixture has reached a temperature below 300°C.

14. A method according to any of claims 10 - 13, wherein filler materia added to the mixture of metallic powder and abrasive particles (5) before the sinti operation and wherein the filler material comprises graphite.

Description:
A GRINDING TOOL FOR MACHINING BRITTLE MATERIALS AND A METHOD OF MAKING A GRINDING TOOL

FIELD OF THE INVENTION

The invention relates to a grinding tool, in particular a grinding tool for grinding hard and/or brittle materials such as tungsten carbide. The grinding tool may in particular be a grinding wheel. The invention also relates to a method of making such a grinding tool. BACKGROUND OF THE INVENTION

Grinding tools such as grinding wheels are used for machining of brittle materials. One area where such grinding tools are used is machining of tools that are made of hard metal (tungsten carbide). For example, grinding tools may be used for machining operations in which drills or milling tools are shaped by grinding. If the work piece which is to be shaped is made of a hard material such as tungsten carbide, the abrasive tool must have abrasive particles of a very hard material. In practice, this normally means that the abrasive particles are diamond particles or grains of cubic boron nitride. Diamonds or cubic boron nitride grains for this purpose are commercially available and can be considered as standard components. Diamonds for this purpose may typically have an average or mean particle size of 50μιη (the size of the particles is of course varying) and have a plurality of sharp edges that can cut hard materials such as tungsten carbide.

A known type of grinding tool for this purpose is a grinding wheel with a core which may be made of, for example, a metallic material such as steel or aluminum. The core may also be made of a non-metallic material such as a polymeric material. The core can be shaped as a disc which can be mounted on a tool spindle for rotation about the axis of the disc-shaped metal core. An abrasive rim surrounds the core and is joined to the core. The abrasive rim may comprise abrasive particles embedded in a matrix with one or more bonding agents. The material used in the abrasive rim is normally more expensive than the material of the core. For this reason, the abrasive rim has a smaller extension in the radial direction than the core (i.e. the abrasive rim is normally a smaller part of the grinding wheel since it is more expensive). During grinding, the abrasive rim is gradually worn down until it is consumed and the grinding wheel can no longer be used. Known bonding agents for abrasive rims of grinding wheels include polymeric b agents such as, for example, Bakelite. Alternatively, the bonding agent may be a ceramic bonding agent. It is also known to use metallic bonding agents, in particu bonding agents of bronze that have been made by sintering. In such sintering opei metal powder containing copper and tin is sintered together with abrasive particle as diamond particles or grains of cubic boron nitride. Sometimes, silver can be ad such that the bronze contains copper (Cu), tin (Sn) and silver (Ag). In the past, pr; experience has showed that Cu/Sn/Ag alloys function well as bonding agents for abrasives and that such bonding agents function well during grinding. Although tl precise reason for this is not entirely understood, it is believed by the inventors th improved thermal conductivity caused by the addition of silver may explain why alloys comprising silver function well as bonding agents for abrasives. However, silver is expensive, other bronze alloys may be used in order to reduce the cost an present invention is applicable also to bronze alloys without silver.

Other known bronze compositions for this purpose include copper/tin/cobalt (Cu/ and copper/tin/nickel (Cu/Sn/Ni). It has also been suggested that bronze composit for this purpose may include copper/tin/titanium (Cu/Sn/Ti). Yet another known system includes hybrids of polymeric and metallic bonding a£ in which metallic powder is sintered together with polymeric material such that a is formed in which the polymeric bonding agent and the metallic bonding agent (typically a bronze alloy as described above) are closely intertwined with each otl a microscopic level. In such hybrids, the metal bonding agent and the polymeric bonding agent each forms a network and the respective networks of the bonding a penetrate each other. Such a hybrid matrix that comprises both a metal bonding a\ and a polymeric bonding agent is disclosed in for example US patent No. 606314

In addition to metallic and polymeric bonding agents, such hybrids normally inch one or several fillers. One such filler may be graphite which is used for its lubrica properties.

The abrasive particles used may have different properties. For example, the brittk of diamonds may vary depending on the purpose for which the grinding tool is to used. The properties of different diamonds may be matched to meet the properties different bonding agents (or hybrids of bonding agents). In a good grinding tool, the abrasive particles should be bonded in its matrix in su way that the grinding tool functions as desired. It is desirable that the grinding toe a good resistance to wear such that it can be used over an extended period. Howe 1 good wear resistance is not the only desired property and the grinding tool with tt highest resistance to wear is not necessarily the best choice. Other desirable propt include low energy consumption (i.e. that the power required to drive the grinding is not excessively high) and constant or at least predictable performance propertie the grinding effect of the abrasive rim varies too much over time, this causes prob This is especially the case if the performance of the grinding tool varies in a way unpredictable.

The extent of wear of the grinding tool under given circumstances depends to a v< high degree on the properties of the matrix in which the abrasive particles are embedded. Therefore, the composition of the matrix is important.

When a grinding tool is used for machining a work piece, sharp corners and edge: the abrasive particles act on the work piece. Thereby, force is exerted on abrasive particles embedded in the matrix. During the grinding, the abrasive particles are damaged. Gradually, small pieces break loose from the abrasive particles such th abrasive particles are gradually worn down. When the abrasive particles in one ar the abrasive rim have been completely worn down, the work piece meets the mati directly. The matrix as such is less hard than the work piece and it is quickly won down. As a result, fresh abrasive particles come to the surface of the abrasive rim can start to act on the work piece.

However, if the matrix that holds the abrasive particles is too weak, abrasive parti may be torn away from the matrix before they have been worn down. When this happens in part of the surface of the abrasive rim, the work piece will come into c contact with the relatively brittle matrix and wear down the matrix prematurely. this happens, power consumption drops momentarily until so much of the matrix been worn down that fresh abrasive particles come to the surface. As a result, the abrasive rim of the grinding tool is worn out faster than it would otherwise have b the operation of the grinding tool has been programmed in advance, the conseque thereof may be that the grinding operation does not function properly since the gr tool is set to operate based on an assumption of tool diameter that is now incorrec problem becomes more serious if the abrasive rim is worn out in a way that is difi to predict, for example if wear occurs in sudden stens that come in irreeular inten It is also desirable that the required power for the grinding operation can be kept 1 such that the energy consumption during grinding can be minimized. Another desirable property of grinding tools is a high G-ratio. The G-ratio expres; ratio between the volume of the material removed by the grinding tool from a wo: piece and the volume lost by the grinding tool (the wear on the tool). A good grin tool has a high G-ratio. Therefore, it is an object of the present invention to provide a grinding tool that h; good resistance to wear. Further objects of the invention are to provide a tool that worn out in a regular and predictable way, which has a low power requirement an high G-ratio. These objects are achieved by means of the present invention as wil explained in the following.

SUMMARY OF THE INVENTION

The invention relates to a grinding tool. The grinding tool is especially intended a grinding tool for machining hard and/or brittle materials, such as tungsten carbide the inventive grinding tool could also be used for grinding other materials. The gr tool comprises a core and an abrasive rim. The abrasive rim comprises abrasive p embedded in a matrix and the matrix comprises a metallic bonding agent which is sintered bronze alloy. The metallic bonding agent constitutes 50 % - 100 % by vo of the matrix. According to the invention, the metallic bonding agent contains sili nitride in an amount that constitutes 0.02 % - 5.0 % by volume of the metallic bot agent or optionally 0.1 % by volume - 5.0 % by volume of the metallic bonding a

In embodiments of the invention, the matrix may further optionally comprise a polymeric bonding agent that has been sintered together with the metallic bondinj such that the polymeric bonding agent and the metallic bonding agent form a com network.

In embodiments of the invention, the silicon nitride constitutes 0.3 % - 5.0 % by -\ of the metallic bonding agent. For example, it may constitute 0.5 % - 5.0 % by vo of the metallic bonding agent, 1.0 % - 5.0 % by volume of the metallic bonding a or 0.5 % - 3.0 % by volume or 0.5 % - 2.0 % by volume. The silicon nitride may be present in the shape of grains having an average grain which is preferably less than ΙΟμιη but also preferably above Ο. ΐμιη. Such particli be 1250 Tyler mesh particles. The particles may thus include particles up to ΙΟμη though average grain size is smaller.

When a polymeric bonding agent is part of the matrix, the polymeric bonding age comprise polyimide or be made entirely or almost entirely of polyimide.

The matrix may optionally additionally comprise filler materials such as graphite. Graphite has lubricating properties which may be desirable during grinding.

The metallic bonding agent is preferably a bronze alloy that comprises copper, tin silver. The abrasive particles may be, for example, diamond particles or cubic boron nitr particles. For both diamonds and cubic boron nitride, the abrasive particles may h mean particle size in the range of 4μπι - 18 Ιμπι. In many realistic embodiments, abrasive particles may have a size in the range of 46μπι - 91μπι. In embodiments invention, the abrasive particles may have a coating of copper or nickel.

The invention also relates to a method of making the inventive grinding tool. The method comprises sintering abrasive particles together with metallic powder such the sintering results in a matrix in which the abrasive particles are embedded. The matrix will thereby comprise a metallic bonding agent. The metallic powder com] copper and tin such that the metallic bonding agent will be a sintered bronze allo According to the invention, silicon nitride in the form of a powder is added to the metallic powder before sintering and to such an extent that the silicon nitride will constitute 0.02 % - 5.0 % by volume of the metallic bonding agent and preferably - 5.0% by volume of the metallic bonding agent.

In embodiments of the inventive method, the metallic powder may additionally comprise silver.

When reference is made to the relative proportion of silicon nitride in the metal bi agent, it should be understood that this refers to the volume proportion of the pow used in the manufacturing process. In other words, the method of manufacturing i that, in the powder added before sinterine. silicon nitride will constitute 0.02 % - by volume of the metallic bonding agent (the silicon nitride being counted as part metal bonding agent). It is assumed that the silicon carbide particles will retain th relative proportion of total volume also after sintering. Optionally, a polymer is added to the metallic powder before sintering, preferabl} form of polyimide powder, such that also a polymeric bonding agent is formed wl a part of the matrix.

The method may be carried out in such a way that the powder material for the bot agents of the matrix is mixed with the abrasive particles to form a mixture. The m is then compacted in a cold press. The compacted mixture is then cured in a kiln∑ temperature in the range of 380°C - 520°C, preferably 400°C - 500°C, for a perio 120 - 150 minutes. Thereafter, the compacted and cured mixture is placed in a pri subjected to a pressure of 1500 - 2000 kg/cm 2 . The pressure is then held until the mixture has reached a temperature below 300°C.

Optionally, filler material is added to the mixture of metallic powder and abrasive particles before the sintering operation. The filler material may optionally compri graphite.

The matrix of the inventive grinding tool may advantageously be a matrix which : hybrid, i.e. a matrix having both a metal bonding agent and a polymeric bonding ; Hybrid bonding solutions can combine the best properties of metal bonding agent the best properties of polymeric bonding agents. If re-sharpening by a sharpening needed, a grinding tool with a hybrid matrix can be re-sharpened easier than a pui metal matrix. At the same time, a grinding tool with a hybrid matrix has better resistance to wear than a matrix using only a polymeric bonding agent.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 is a schematic representation of a grinding tool.

Figure 2 is a schematic cross sectional representation of abrasive particles embedded in the abrasive rim of a grinding tool.

Figure 3 is a schematic cross sectional representation of a grinding tool that z

a work piece.

Figure 4 is a diagram that represents the power consumption for two differen grinding tools. Figure 5 is a schematic cross sectional representation of a first embodiment c inventive grinding tool.

Figure 6 is a schematic cross sectional representation of a second embodimer the inventive grinding tool.

Figure 7 is a diagram that shows wear of a grinding tool as a function of silic nitride content.

Figure 8 is a diagram that shows the G-ration of a grinding tool as a function silicon nitride content. DETAILED DESCRIPTION OF THE INVENTION

With reference to Figure 1, a grinding tool 1 is shown. The grinding tool may in particular be a grinding wheel which is intended for machining hard and/or brittle materials such as tungsten carbide. Such materials may be present in work pieces tools such as for example drills or milling tools and the grinding tool 1 of the pres invention may be a grinding wheel that is used for shaping such tools. The grindii 1 comprises a core 2 and an abrasive rim 4. The core 2 may be made of a less exp material such as steel or some other metal. Alternatively, the core could be made example, a polymeric material. The core could also comprise more than one mate For example, it could be made partially by metal such as steel or aluminum and p be a polymeric material. The core 2 may be provided with a through-hole or cavit such that the grinding tool 1 may be mounted on a spindle (not shown) for rotary movement. With reference to Figure 2, the abrasive rim 4 comprises abrasive pari embedded in a matrix 6. The matrix 6 in turn comprises a metallic bonding agent is a sintered bronze alloy. The metallic bonding agent constitutes 50 % - 100 % b; volume of the matrix 6 and embodiments are thus conceivable in which the entire matrix 6 is made up of the metallic bonding agent. However, the matrix 6 normal! comprises at least some other component. For example, it may comprise filler sue graphite that has lubricating properties. In most embodiments, the matrix 6 would comprise a polymeric bonding agent that may be formed by polyimide.

If the matrix 6 holds the abrasive particles 5 well, the abrasive particles 5 will em small fragments and be worn down gradually. As a result, the wear on the abrasiv 4 will be relatively slow such that the diameter of the grinding tool 1 can be kept substantially constant during a longer period. Moreover, wear on the abrasive rim be kept at an even pace and the power during operation will not vary so much. If the matrix 6 is instead incapable of holding the abrasive particles 5 firmly, it mi happen that abrasive particles come loose well before they have been fragmented, consequence, they will be lost before their entire abrasive potential has been used abrasive tool 1 will be worn out faster and the diameter of the grinding tool (such grinding wheel) will decrease faster. A smaller diameter of the grinding tool 1 ma result in a less accurate machining of the work pieces.

With reference to Figure 3, a grinding tool 1 acts on a work piece 7. The work pie may be, for example, a work piece that shall be shaped to a drill. The grinding toe rotated by means of a power source acting through for example a spindle (not sho Thereby, the abrasive rim 4 of the grinding tool acts on the work piece 7 to cut a \ in the work piece. In Figure 3, the work piece has a core diameter CD which is determined by the action of the grinding tool 1. If the grinding tool 1 is worn dow that its diameter decreases, the core diameter CD will grow unless the wear is compensated (for example by repositioning of the grinding tool 1 in relation to th piece 7). It is therefore very desirable that the wear can be kept low and that the w that does take place does not come in sudden unpredictable leaps.

It can be added that, when the abrasive particles 5 are properly fragmented piece 1 piece, this is good for the free-cutting properties of the grinding tool 1, i.e. the abi the grinding tool to re-sharpen itself. When the abrasive particles 5 become fragm step by step, the wear on the matrix 6 can occur smoothly and the surface of the abrasive rim 4 does not become clogged so easily. If abrasive particles are insteac away suddenly before they have been properly fragmented, this tends to lead to increased clogging of the surface; the surface of the abrasive rim 4 may become c to a greater extent by small particles 5 from the work piece 7. This may necessital temporary removal of the grinding tool 1 from operation such that the grinding to may be re-sharpened. If the abrasive particles 5 are gradually fragmented, the risk such clogging is smaller. When abrasive particles have been completely worn out abrasive particles 5 may come to surface in a smoother process which in itself contributes to re-sharpening of the grinding tool (or rather the abrasive rim 4 of tt grinding tool 1).

When abrasive particles are torn away from the abrasive rim before they have bee completely fragmented, this tends to show itself in the power consumption of the grinding tool; the power suddenly drops and then starts to rise again after a while, abrasive particles are held nronerlv bv the matrix so that thev are allowed to fragr they should, also this can be seen on the power consumption. In such a case, the p tends to remain relatively constant over time (it should be noted, however, that tfr normally always a gradual increase in the power requirement from the first work such that less power is required for the very first work pieces).

It has been suggested in an article by E. D. Kizikov and P. Kebko ("Microadditio, alloys of the system Cu-Sn-Tf Institute of Superhard Materials, Academy of Sck the Ukrainian SSR, Kiev, in translation from Metallovedenie I Termicheskaya Obrabotka Metallov, No. 1, pp 50 - 53, January 1987) that an alloy of Cu/Sn/Ti v is to be used as binder for diamond-abrasive tools be reinforced with 0.01% silicc nitride (S1 3 N 4 ). According to the authors of that article, this addition resulted in improved yield strength.

The inventors of the present invention have considered what steps can be taken tc improve the ability of the matrix to hold the abrasive particles. Without wishing fc bound by theory, the inventors believe that one reason that metal bonding agents 1 the abrasive particles embedded therein may be that dislocations inside the metal bonding agent weaken the metallic bonding agent. Assuming this theory to be coi the inventors first speculated that it should be possible to improve the matrix by reinforcing it with particles blocking dislocations in the metal bonding agent.

Consequently, the inventors tried different additions to the metal powder that was for sintering the metal bonding agent. One additive that was tried was aluminum < which was added to an extent corresponding to 1.0 % by volume of the metal bon agent. This resulted in a certain improvement but the improvement was not as goc the inventors had hoped. The inventors also tried addition of 0.01 % by volume oi silicon nitride. The improvement of that addition was even less than the improver achieved by the aluminum oxide.

The inventors then investigated whether increased amounts of silicon nitride wou produce better results. This was confirmed in testes carried out by the inventors. silicon nitride was added in quantities significantly larger than 0.01 % by volume metal bonding agent, it was discovered that a very substantial improvement was obtained. For example, the inventors tested a composition in which the metal bonding agen contained 1.0 % by volume of silicon nitride (S1 3 N 4 ). A grinding tool with this composition was then comnared to a standard erindine tool usine a hvbrid matrix which did not contain silicon nitride (Si 3 N 4 ). The grinding tools were both grindii wheels in which the abrasive rim 4 was shaped as a ring surrounding the core 2. 1 comparable conditions, the diameter of the standard tool was worn down by 136μ while the diameter of the grinding tool with the experimental composition was w( down by only 58μιη. The G-ratio for the tool with 1.0 % silicon nitride was 2335. comparison, a tool using 0.01 % by volume of silicon nitride was worn down 94μ while a tool using 1.0 % by volume aluminum oxide was worn down 84μιη.

A test was made with a composition where silicon nitride constituted 5 % by volu the metal bonding agent. The resistance to wear was still good but not quite as go for the grinding tool with 1.0% by volume silicon nitride. Moreover, the tool with silicon nitride had higher power consumption. The G-ratio was good but not quite good as for the tools with 1.0% and 0.1 % by volume. The inventors have also tested a grinding wheel which had a shape and a composi similar to the other tools tested but in which the silicon nitride constituted 0.1 % 1 volume of the metal bonding agent. It was found that, under the same test conditi< the other tools that were tested, the wear of the tool with 0.1 % by volume silicon was 62μιη and the G-ration was 2084. While this was inferior to the results obtair 1 % by volume, it was still a very substantial improvement compared to the stand grinding tool.

The inventors have also tested a grinding wheel which had a silicon nitride conter 0.02 % by volume of the metal bonding agent but which was otherwise similar to other grinding wheels tested. Under similar test conditions, the grinding wheel wi % by volume of silicon nitride has a wear (diameter reduction) of 58μιη and a G-i 2283. The results were thus slightly better than the results obtained at a ratio of 0. by volume. The results lead to the conclusion that significantly better results are obtained in tl range of 0.02 % - 5.0 % by volume silicon nitride (S1 3 N 4 ). In this range, both G-n and resistance to wear has been found to be significantly better than at 0% or 0.01

Tests of resistance to wear and test of G-ratio have been carried out at 0 % by vol 0.01 % by volume, 0.02 % by volume, 1.0 % by volume and 5.0 % by volume sili nitride. The tools that were tested were grinding wheels of substantially the kind shown ii Figure 5, i.e. grinding tools with an abrasive rim 4 that surrounds a core 2 and wh grinding tool 1 rotates about the axis A during operation. Resistance to wear as a function of silicon nitride content can be seen in Figure 7. The resistance to wear expressed in Figure 7 as diameter reduction. As can be seen in Figure 7, resistanc wear increased significantly when the content of silicon nitride was increased froi % to 0.02 %. The wear resistance continued to be high up to a silicon nitride cont 5.0 % by volume of the metallic bonding agent. However, at 5.0 % by volume sili nitride, the resistance to wear was somewhat lower compared to the resistance ob; at a content of 0.02 % - 1.0 %. The inventors have therefore concluded that the be wear resistance is obtained in the range of 0.02 % - 5.0 % by volume.

The G-ratio as a function of silicon nitride content can be seen in Figure 8. As cai seen in the figure, the best values are obtained at a silicon nitride content in the ra 0.02 % - 5.0%. From Figure 8, it can also be derived that the G-ratio is sinking to the right in the figure even though the G-ratio at 5.0% by volume is still good.

Therefore, the inventors have concluded that the metallic bonding agent may conl silicon nitride in an amount that constitutes 0.02 % - 5.0 % by volume of the mete bonding agent. Since power consumption was higher at 5.0 % by volume, the inv have concluded that values lower than 5.0% will have good resistance to wear bui power consumption compared to tools with a silicon nitride content of 5% by voli Therefore, a preferred range may be 0.02 % by volume to 3.0% by volume, 0.5 % % by volume, 0.5 % - 2.0 % by volume or 1.0 % - 2.0 % by volume of the metalli bonding agent.

At 0.1 % by volume, power consumption was generally lower than at 0.02 % by volume. At a silicon nitride of 5.0 % by volume, power consumption was higher 1 a content of 0.02 % but the power consumption at 5.0 % by volume was more eve power consumption was more predictable than at 0.02 % by volume.

The silicon nitride particles should preferably have a size up to ΙΟμπι (1250 Tylei mesh). For sieved particles, this will normally mean that average grain size is less ΙΟμπι. The average particle size (D50) of the silicon nitride particles may then be 2μπι - 3μπι (depending on how average particle size is measured). The specific su area of the silicon nitride particles may advantageously be in the range of 5 m 2 /g - m 2 /g. If the particles used are too small, this mav result in cloeeine and difficultie during manufacturing. Moreover, for giving optimized strength to the metal bond agent, it is believed by the inventors that particles up to ΙΟμιη should preferably b included. Normally, the matrix 6 should further comprise a polymeric bonding agent that h< sintered together with the metallic bonding agent such that the polymeric bonding and the metallic bonding agent form a connected network (even though such a polymeric bonding agent is optional). The use of a polymeric agent makes it poss fine tune the properties of the matrix and adapt it to different kinds of abrasive pa The polymeric bonding agent may suitably be polyimide or comprise polyimide. ' reason for this is that polyimide is heat resistant and can withstand the high temperatures during sintering. If a polymeric bonding agent is used, the polymerii bonding agent may be present in an amount of up to 50% by volume of the matri? the amount of polymeric bonding agent is in the range of 0% - 50% by volume of matrix). For example, the polymeric bonding agent may represent 10 % - 40 % oi 30% by volume of the matrix.

Possibly, the polymeric bonding agent could be formed by some other polymeric material. For example, it could be formed by polyamide-imide which is also capa withstanding high temperatures. However, polyimide is preferred since it has bett grinding properties than polyamide-imide.

The metallic bonding agent is a preferably a bronze alloy that comprises copper, t silver. Silver improves the desirable properties of the metal bonding agent.

The abrasive particles 5 may be either diamond particles or cubic boron nitride p∑ Diamonds are harder and have better abrasive properties but cubic boron nitride i: temperature resistant. Moreover, diamonds may react chemically with certain ma1 The abrasive particles 5 may be are diamond particles or particles of cubic boron nitride. The particles may be in the range of 4μπι - 18 Ιμτη even though particles c this range may be considered depending on the requirements in each specific case many realistic embodiments, the abrasive particles 5 may have a mean particle si the range of 46μπι - 91 μπι which is a range that is suitable for many grinding operations. The abrasive particles 5 may optionally have a coating of copper or nickel. A coa copper or nickel can improve the bond between the abrasive particles 5 and the m 6. However, the abrasive properties of the particles 5 will be somewhat reduced ii particles have such a coating.

The relative proportion of abrasive particles 5 in relation to the bonding agents an fillers in the matrix 6 may vary depending on the requirements in each case. In mi realistic embodiments, the amount of abrasive particles may represent a 10 % - 5( the total volume of the abrasive rim (i.e. the total volume of the abrasive particles the matrix). If the relative proportion of abrasive particles is higher than 50 %, tt substantial danger that the matrix will no longer be able to hold the abrasive partii the relative proportion of abrasive particles is less than 10 %, the grinding effect r become too small. The relative proportion of abrasive particles may preferably be range of 15 % - 30 % and a suitable value may be 25 %.

Preferably, the silicon nitride is present in the shape of grains having an average £ size which is equal to or less than ΙΟμπι but above 0.1 μπι. For example, they may a mean size in the range of Ι μτη - ΙΟμπι or 2μπι - 9μπι . It is believed by the inver that silicon nitride particles smaller than 0.1 μπι may result in clogging of the silic nitride particles which reduces their reinforcing effect.

The silicon nitride particles may have three different crystallographic structures designated as α, β and γ phases (also known as trigonal phase, hexagonal phase ai cubic phase). The a and β phases are the most common. The γ phase can only be synthesized under high pressure and high temperature. Any of these phases can b< Preferably, the phase used is the a phase. The silicon nitride particles added may ; a mixture of particles of different phases.

With reference to Figure 4, a grinding tool according to the invention is comparec a standard grinding tool. The vertical axis represents power consumption while th horizontal axis represents number of work pieces upon which the respective grind tool has acted. In Figure 4, B5 represents a grinding tool according to the inventic while EZ represents a standard grinding tool. As can be seen in Figure 4, the tool represented as B5 has a power consumption that first rises steeply and thereafter remains substantially constant. The conventional tool as represented by EZ has a consumption that rises steeply and then suddenly drops before it rises again. This indicates that the abrasive narticles of the B5 tool are slowlv fragmented while Έ/ represents a grinding tool where the abrasive particles are suddenly torn away. Tr on the tool will therefore be faster.

It can be added that B5 represents a tool with both a metal bonding agent and a polymeric bonding agent. The metal bonding agent is a bronze that has copper, til silver. It has been sintered using a metal powder that contains 45 % by volume co 45 % by volume tin and 10 % by volume silver. In the tool according to B5, the polymeric bonding agent constitutes 1.0 % by volume of the total amount of bone agent.

The grinding tool of Figure 1 may have a cross section as shown in Figure 5. In si embodiment, the abrasive rim 4 is placed radially outside the core 2 such that the completely surrounds the core 2. The tests explained with reference to Figure 4, 1 7 and Figure 8 have been carried out on such a grinding tool. However, the invenl not limited to such an embodiment. With reference to Figure 6, it should be undei that the core 2 may extend at least as much in the radial direction as the abrasive i In Figure 6, the grinding tool has an abrasive rim 4 that does not extend beyond tl 2 in the radial direction. Instead, the abrasive rim 4 has an extension in the axial direction that is different from that of the core 2 (the axial direction being the axis rotation A of the grinding tool 1 when it is driven by a spindle, see Figure 5 and F 6). It should also be understood that the grinding tool 1 is not necessarily designei rotation. Instead, it could act on work pieces in a reciprocating movement. In the context of the claims, the term "core" should thus be understood broadly as any k carrier body for the abrasive rim. Likewise, the term "rim" should also be underst broadly as any kind of layer secured to the core 2 such that abrasive particles can a work piece.

The invention further comprises a method of making the inventive grinding tool, method comprises sintering abrasive particles together with metallic powder that comprises copper and tin such that the sintering results in a matrix in which the al particles 5 are embedded. The matrix comprises a metallic bonding agent which i; sintered bronze alloy. According to the invention, silicon nitride in the form of a j is added to the metallic powder before sintering to such an extent that the silicon i will constitute 0.1% - 5.0% by volume of the metallic bonding agent.

The metal powder used is preferably metal powder with particles that are smaller 44μπι but they should nreferablv be lareer than the silicon nitride narticles. Prefer they should be at least twice as large. An average size in the range of 15μιη - 44μ be suitable.

The metallic powder may optionally also comprise silver.

The metal powder may come in the shape of pre-alloyed particles or as particles c copper, pure tin, pure silver etc.

A polymer may be added to the metallic powder before sintering, preferably in th of polyimide powder, such that also a polymeric bonding agent is formed which i part of the matrix 6.

The sintering method may be carried out such that the powder material for the boi agents of the matrix 6 is mixed with the abrasive particles 5. The mixture is comp in a cold press. Thereafter the compacted is mixture is cured in a kiln at a tempen the range of 380°C - 520°C, preferably 400°C - 500°C or 440°C - 460°C, for a pe 120 - 150 minutes. The time required depends on size. In a larger press form, mo is required. Thereafter (preferably immediately thereafter) the compacted and cur mixture is placed in a press and subjected to a pressure of 1500 - 2000 kg/cm 2 Tt pressure is then maintained until the mixture has reached a temperature below 30<

For example, the inventors have made grinding tools according to this method in process where the temperature in the kiln was 450°C. The abrasive rim 4 may also be manufactured by means of spark plasma sintering (SPS). By this technique, the abrasive rim 4 may be manufactured very fast.

The rim with the matrix containing abrasive particles may be sintered separately∑ subsequently fastened (e.g. glued) onto the core 2. Alternatively, the abrasive rim be sintered directly onto the core 2 such that it is bonded to the core as it is forme Before sintering, the core 2 may be electrolytically plated with copper on at least surface of the core which will meet the abrasive rim 4. The abrasive rim 4 can the sintered onto the copper-plated surface such that a seam is formed. Filler material may optionally be added to the mixture of metallic powder and abi particles 5 before the sintering operation. As previously explained, the filler mate: may comprise graphite. Other possible filler materials may include, for example, spheres of aluminum oxide.

Preferably, the bronze used in the metal bonding agent is selected from the group including copper - tin (Cu/Sn), copper - tin - cobalt (Cu/Sn/Co), copper - tin - r (Cu/Sn/Ni) or copper - tin - silver (Cu/Sn/ Ag). Even more preferred, the bronze i copper - tin - silver bronze. Other bronze alloys can also be considered.

The inventive grinding tool can be used for machining hard and/or brittle material This does not exclude the possibility that the grinding tool can be used also for ot materials.

In embodiments of the invention, the matrix 6 may optionally also comprise at le∑ ceramic component in the shape of ceramic particles. The ceramic component ma for example, frit and contain Si0 2 . Ceramic particles for the matrix may be frit in shape of spherical particles having a particle size of 50μπι - 500μπι depending on size of the abrasive particles. For larger abrasive particles, larger ceramic particle; be used. The abrasive particles may be embedded in the ceramic particles while tl ceramic particles are embedded in a hybrid matrix with a metallic bonding agent < polymeric bonding agent. The ceramic particles may be held stronger by the matr the abrasive particles would be held. The free-cutting properties of the abrasive ri thus improved. The ceramic component does not have such a good resistance to v the metallic bonding agent. By combining ceramics, metal and polymeric bonding agents, it is possible to combine the best properties of these bonding agents.