NZ620302B2 - A grinding tool for machining brittle materials and a method of making a grinding tool - Google Patents
A grinding tool for machining brittle materials and a method of making a grinding tool Download PDFInfo
- Publication number
- NZ620302B2 NZ620302B2 NZ620302A NZ62030212A NZ620302B2 NZ 620302 B2 NZ620302 B2 NZ 620302B2 NZ 620302 A NZ620302 A NZ 620302A NZ 62030212 A NZ62030212 A NZ 62030212A NZ 620302 B2 NZ620302 B2 NZ 620302B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- grinding tool
- bonding agent
- matrix
- volume
- silicon nitride
- Prior art date
Links
- 238000000227 grinding Methods 0.000 title claims abstract description 131
- 239000000463 material Substances 0.000 title claims abstract description 37
- 238000003754 machining Methods 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 239000002245 particle Substances 0.000 claims abstract description 121
- 239000011159 matrix material Substances 0.000 claims abstract description 73
- 229910052581 Si3N4 Inorganic materials 0.000 claims abstract description 54
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical group N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims abstract description 54
- 239000000843 powder Substances 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 24
- 229910000906 Bronze Inorganic materials 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 21
- 239000007767 bonding agent Substances 0.000 claims description 102
- 239000010949 copper Substances 0.000 claims description 26
- 239000011135 tin Substances 0.000 claims description 23
- 238000005245 sintering Methods 0.000 claims description 21
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 17
- 229910052802 copper Inorganic materials 0.000 claims description 17
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 15
- 229910052709 silver Inorganic materials 0.000 claims description 15
- 239000004332 silver Substances 0.000 claims description 15
- 229910052718 tin Inorganic materials 0.000 claims description 14
- 239000010432 diamond Substances 0.000 claims description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 11
- 239000000945 filler Substances 0.000 claims description 11
- 229910052582 BN Inorganic materials 0.000 claims description 9
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 9
- 239000004642 Polyimide Substances 0.000 claims description 9
- 229920001721 polyimide Polymers 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 229910002804 graphite Inorganic materials 0.000 claims description 8
- 239000010439 graphite Substances 0.000 claims description 8
- 229910003460 diamond Inorganic materials 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 abstract description 35
- 239000002184 metal Substances 0.000 abstract description 35
- 229910045601 alloy Inorganic materials 0.000 abstract description 5
- 239000000956 alloy Substances 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 description 14
- 239000000919 ceramic Substances 0.000 description 9
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 9
- 239000010974 bronze Substances 0.000 description 8
- 150000002500 ions Chemical class 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 150000004767 nitrides Chemical class 0.000 description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 239000004962 Polyamide-imide Substances 0.000 description 2
- PQIJHIWFHSVPMH-UHFFFAOYSA-N [Cu].[Ag].[Sn] Chemical compound [Cu].[Ag].[Sn] PQIJHIWFHSVPMH-UHFFFAOYSA-N 0.000 description 2
- 239000003082 abrasive agent Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 229910001128 Sn alloy Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- ZJHIEQGQFJJLBM-UHFFFAOYSA-N [Co].[Sn].[Cu] Chemical compound [Co].[Sn].[Cu] ZJHIEQGQFJJLBM-UHFFFAOYSA-N 0.000 description 1
- VRUVRQYVUDCDMT-UHFFFAOYSA-N [Sn].[Ni].[Cu] Chemical compound [Sn].[Ni].[Cu] VRUVRQYVUDCDMT-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- -1 for example Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000002490 spark plasma sintering Methods 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
Classifications
-
- B22F1/025—
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/02—Compacting only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D18/00—Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for
- B24D18/0009—Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for using moulds or presses
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
- B24D3/02—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
- B24D3/04—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic
- B24D3/06—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic metallic or mixture of metals with ceramic materials, e.g. hard metals, "cermets", cements
- B24D3/08—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic metallic or mixture of metals with ceramic materials, e.g. hard metals, "cermets", cements for close-grained structure, e.g. using metal with low melting point
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
- B24D3/02—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
- B24D3/20—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic
- B24D3/28—Resins or natural or synthetic macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
- B24D3/34—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties
- B24D3/342—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties incorporated in the bonding agent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D5/00—Bonded abrasive wheels, or wheels with inserted abrasive blocks, designed for acting only by their periphery; Bushings or mountings therefor
- B24D5/02—Wheels in one piece
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D5/00—Bonded abrasive wheels, or wheels with inserted abrasive blocks, designed for acting only by their periphery; Bushings or mountings therefor
- B24D5/06—Bonded abrasive wheels, or wheels with inserted abrasive blocks, designed for acting only by their periphery; Bushings or mountings therefor with inserted abrasive blocks, e.g. segmental
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D7/00—Bonded abrasive wheels, or wheels with inserted abrasive blocks, designed for acting otherwise than only by their periphery, e.g. by the front face; Bushings or mountings therefor
- B24D7/06—Bonded abrasive wheels, or wheels with inserted abrasive blocks, designed for acting otherwise than only by their periphery, e.g. by the front face; Bushings or mountings therefor with inserted abrasive blocks, e.g. segmental
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D99/00—Subject matter not provided for in other groups of this subclass
- B24D99/005—Segments of abrasive wheels
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/05—Mixtures of metal powder with non-metallic powder
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
- C22C32/0047—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
- C22C32/0068—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only nitrides
Abstract
The specification 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 sintered bronze alloy. The alloy comprises 50 to 100% of the volume of the matrix. 0.02% -5.0 % by volume of the alloy is silicon nitride in the shape of grains having an average grain size which is between 1 ?m and 10?m. 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. me of the matrix. 0.02% -5.0 % by volume of the alloy is silicon nitride in the shape of grains having an average grain size which is between 1 ?m and 10?m. 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.
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 ng tool, in particular a grinding tool for grinding hard
and/or brittle materials such as tungsten carbide. The grinding tool may in ular 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
ions 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 ve
tool must have abrasive particles of a very hard material. In practice, this normally
means that the abrasive particles are diamond les or grains of cubic boron nitride.
Diamonds or cubic boron nitride grains for this purpose are commercially available and
can be considered as rd components. Diamonds for this purpose may typically
have an average or mean particle size of 50pm (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 ric 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 se abrasive particles embedded in a matrix with one
or more bonding agents. The material used in the abrasive rim is normally more
ive 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 r
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 bonding
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 particular
g agents of bronze that have been made by sintering. In such sintering operations,
metal powder containing copper and tin is sintered er with abrasive particles such
as diamond particles or grains of cubic boron nitride. Sometimes, silver can be added
such that the bronze contains copper (Cu), tin (Sn) and silver (Ag). In the past, cal
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 the
precise reason for this is not entirely understood, it is believed by the ors that
improved thermal conductivity caused by the addition of silver may explain why bronze
alloys sing silver function well as bonding agents for abrasives. However, since
silver is expensive, other bronze alloys may be used in order to reduce the cost and the
present invention is applicable also to bronze alloys without silver.
Other known bronze compositions for this purpose e copper/tin/cobalt (Cu/Sn/Co)
and /tin/nickel (Cu/Sn/Ni). It has also been suggested that bronze compositions
for this purpose may include /tin/titanium (Cu/Sn/Ti).
Yet another known system includes hybrids of polymeric and metallic bonding agents
in which metallic powder is sintered together with polymeric material such that a matrix
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 other on
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 agents
penetrate each other. Such a hybrid matrix that comprises both a metal g agent
and a polymeric bonding agent is disclosed in for example US patent No. 6063148.
In addition to metallic and polymeric bonding agents, such hybrids normally include
one or several flllers. One such flller may be graphite which is used for its lubricating
properties.
The abrasive particles used may have ent ties. For example, the eness
of diamonds may vary depending on the purpose for which the grinding tool is to be
used. The properties of different diamonds may be matched to meet the properties of
different g agents (or hybrids of bonding agents).
In a good grinding tool, the abrasive particles should be bonded in its matrix in such a
way that the ng tool fiinctions as desired. It is desirable that the grinding tool have
a good resistance to wear such that it can be used over an extended period. However,
good wear resistance is not the only desired property and the grinding tool with the
highest resistance to wear is not necessarily the best choice. Other desirable properties
include low energy consumption (i.e. that the power required to drive the grinding tool
is not excessively high) and constant or at least predictable mance properties. If
the grinding effect of the abrasive rim varies too much over time, this causes problems.
This is especially the case if the performance of the ng tool varies in a way that is
unpredictable.
The extent of wear of the grinding tool under given circumstances depends to a very
high degree on the properties of the matrix in which the abrasive particles are
embedded. Therefore, the ition of the matrix is important.
When a grinding tool is used for machining a work piece, sharp corners and edges on
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 that the
abrasive particles are gradually worn down. When the abrasive particles in one area of
the ve rim have been completely worn down, the work piece meets the matrix
directly. The matrix as such is less hard than the work piece and it is quickly worn
down. As a result, fresh abrasive particles come to the surface of the abrasive rim and
can start to act on the work piece.
However, if the matrix that holds the ve particles is too weak, ve particles
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 direct
contact with the relatively brittle matrix and wear down the matrix prematurely. When
this happens, power ption drops momentarily until so much of the matrix has
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 been. If
the ion of the grinding tool has been programmed in advance, the consequence
thereof may be that the grinding operation does not function properly since the grinding
tool is set to operate based on an tion of tool diameter that is now incorrect. This
m becomes more serious if the abrasive rim is worn out in a way that is difficult
to predict, for example if wear occurs in sudden steps that come in irregular intervals.
WO 15737
It is also desirable that the required power for the grinding operation can be kept low
such that the energy consumption during grinding can be minimized.
Another desirable property of grinding tools is a high G—ratio. The G—ratio expresses the
ratio between the volume of the al removed by the grinding tool from a work
piece and the volume lost by the grinding tool (the wear on the tool). A good grinding
tool has a high G—ratio.
Therefore, it is an object of the t invention to provide a grinding tool that has a
good resistance to wear. Further objects of the invention are to provide a tool that is
worn out in a r and predictable way, which has a low power requirement and a
high G—ratio. These objects are ed by means of the present ion as will be
explained in the following.
SUMIVIARY OF THE ION
The invention relates to a grinding tool. The grinding tool is especially intended as a
grinding tool for machining hard and/or brittle materials, such as tungsten carbide but
the inventive grinding tool could also be used for grinding other materials. The grinding
tool comprises a core and an abrasive rim. The abrasive rim comprises abrasive particles
embedded in a matrix and the matrix comprises a metallic bonding agent which is a
sintered bronze alloy. The metallic bonding agent constitutes 50 % - 100 % by volume
of the matrix. According to the invention, the metallic bonding agent contains silicon
nitride in an amount that constitutes 0.02 % - 5.0 % by volume of the ic bonding
agent or optionally 0.1 % by volume — 5.0 % by volume of the metallic g agent.
In embodiments of the invention, the matrix may further optionally comprise a
polymeric bonding agent that has been ed together with the metallic bonding agent
such that the polymeric bonding agent and the metallic bonding agent form a connected
network.
In embodiments of the invention, the silicon nitride constitutes 0.3 % - 5.0 % by volume
of the ic bonding agent. For e, it may constitute 0.5 % - 5.0 % by volume
of the metallic bonding agent, 1.0 % - 5.0 % by volume of the metallic bonding agent,
or 0.5 % - 3.0 % by volume or 0.5 % - 2.0 % by volume.
The silicon e is present in the shape of grains having an average grain size which
is less than 10μm but also above 1μm. Such particles may be 1250 Tyler mesh particles.
The particles may thus include particles up to 10μm even though average grain size is
smaller.
When a polymeric bonding agent is part of the matrix, the polymeric bonding agent may
comprise polyimide or be made entirely or almost entirely of ide.
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 and
silver.
The abrasive particles may be, for example, diamond particles or cubic boron nitride
particles. For both diamonds and cubic boron nitride, the abrasive particles may have a
mean particle size in the range of 4μm – 181μm. In many realistic embodiments, the
ve particles may have a size in the range of 46μm – 91μm. In ments of the
invention, the abrasive particles may have a coating of copper or nickel.
The invention also s to a method of making the inventive grinding tool comprising
a core and an abrasive rim. The method comprises sintering ve particles together
with metallic powder such that the sintering results in a matrix in which the abrasive
particles are embedded. The matrix will thereby comprise a ic bonding agent. The
metallic powder comprises copper and tin such that the metallic bonding agent will be a
sintered bronze alloy. According to the invention, silicon nitride in the form of a powder
is added to the ic powder before sintering and to such an extent that the silicon
nitride will tute 0.02 % - 5.0 % by volume of the metallic bonding agent and
preferably 0.1% - 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 g
agent, it should be understood that this refers to the volume proportion of the powder
used in the manufacturing process. In other words, the method of manufacturing is such
that, in the powder added before sintering, silicon e will constitute 0.02 % - 5.0%
by volume of the metallic bonding agent (the n nitride being counted as part of the
metal bonding . It is d that the silicon carbide particles will retain the same
relative proportion of total volume also after sintering.
ally, a polymer is added to the metallic powder before sintering, preferably in the
form of polyimide powder, such that also a polymeric bonding agent is formed which is
a part of the matrix.
The method may be carried out in such a way that the powder material for the bonding
agents of the matrix is mixed with the abrasive les to form a mixture. The mixture
is then compacted in a cold press. The compacted e is then cured in a kiln at a
temperature in the range of380°C - 520°C, preferably 400°C - 500°C, for a period of
120 — 150 minutes. Thereafter, the compacted and cured mixture is placed in a press and
subjected to a pressure of 1500 — 2000 kg/cmz. 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 ve
particles before the ing operation. The filler material may optionally comprise
graphite.
The matrix of the inventive grinding tool may advantageously be a matrix which is a
hybrid, i.e. a matrix having both a metal g agent and a polymeric bonding agent.
Hybrid bonding solutions can combine the best properties of metal bonding agents with
the best properties of polymeric bonding agents. If re-sharpening by a sharpening tool is
needed, a grinding tool with a hybrid matrix can be re-sharpened easier than a pure
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 g agent.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure l 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 acts on
a work piece.
Figure 4 is a diagram that represents the power consumption for two different
grinding tools.
Figure 5 is a schematic cross sectional representation of a first embodiment of the
inventive grinding tool.
Figure 6 is a schematic cross nal representation of a second embodiment of
the inventive ng tool.
Figure 7 is a diagram that shows wear of a grinding tool as a function of n
nitride content.
Figure 8 is a diagram that shows the G—ration of a grinding tool as a function of
silicon nitride content.
DETAILED DESCRIPTION OF THE INVENTION
With reference to Figure l, 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
als such as tungsten carbide. Such materials may be present in work pieces for
tools such as for e drills or milling tools and the grinding tool 1 of the present
invention may be a grinding wheel that is used for shaping such tools. The grinding tool
1 comprises a core 2 and an abrasive rim 4. The core 2 may be made of a less expensive
material such as steel or some other metal. Alternatively, the core could be made of, for
example, a polymeric material. The core could also comprise more than one material.
For example, it could be made partially by metal such as steel or aluminum and partially
be a polymeric material. The core 2 may be provided with a through-hole or cavity 3
such that the grinding tool 1 may be mounted on a spindle (not shown) for rotary
movement. With nce to Figure 2, the abrasive rim 4 comprises abrasive particles 5
embedded in a matrix 6. The matrix 6 in turn comprises a ic bonding agent which
is a sintered bronze alloy. The metallic bonding agent constitutes 50 % - lOO % by
volume of the matrix 6 and embodiments are thus conceivable in which the entire
matrix 6 is made up of the metallic bonding agent. r, the matrix 6 normally
ses at least some other component. For example, it may comprise flller such as
graphite that has lubricating properties. In most embodiments, the matrix 6 would also
comprise a polymeric g agent that may be formed by polyimide.
If the matrix 6 holds the abrasive particles 5 well, the abrasive particles 5 will emit
small fragments and be worn down gradually. As a , the wear on the abrasive rim
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 4 will
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 may
happen that abrasive particles come loose well before they have been fragmented. As a
consequence, they will be lost before their entire abrasive potential has been used. The
abrasive tool 1 will be worn out faster and the diameter of the grinding tool (such as a
grinding wheel) will decrease faster. A smaller diameter of the grinding tool 1 may
result in a less accurate machining of the work pieces.
With nce to Figure 3, a grinding tool 1 acts on a work piece 7. The work piece 7
may be, for example, a work piece that shall be shaped to a drill. The grinding tool 1 is
rotated by means of a power source acting through for example a spindle (not shown).
y, the abrasive rim 4 of the grinding tool acts on the work piece 7 to cut a groove
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 down such
that its diameter decreases, the core diameter CD will grow unless the wear is
compensated (for e by repositioning of the grinding tool 1 in relation to the work
piece 7). It is ore very desirable that the wear can be kept low and that the wear
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 by
piece, this is good for the free-cutting properties of the grinding tool 1, i.e. the ability of
the grinding tool to re-sharpen itself. When the ve particles 5 become nted
step by step, the wear on the matrix 6 can occur smoothly and the surface of the
ve rim 4 does not become clogged so easily. If abrasive particles are instead torn
away suddenly before they have been properly fragmented, this tends to lead to
increased ng of the surface, the surface of the abrasive rim 4 may become clogged
to a greater extent by small particles 5 from the work piece 7. This may necessitate
temporary removal of the grinding tool 1 from operation such that the grinding tool 1
may be re-sharpened. If the ve particles 5 are gradually fragmented, the risk of
such clogging is r. When abrasive particles have been completely worn out, new
abrasive particles 5 may come to surface in a smoother process which in itself
contributes to rpening of the grinding tool (or rather the abrasive rim 4 of the
grinding tool 1).
When abrasive particles are torn away from the abrasive rim before they have been
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. If the
abrasive les are held properly by the matrix so that they are allowed to fragment as
they should, also this can be seen on the power consumption. In such a case, the power
tends to remain relatively nt over time (it should be noted, however, that there is
normally always a gradual increase in the power requirement from the first work pieces
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 (“Microaddilions l0
alloys ofthe system T1'”, Institute of Superhard Materials, Academy of Science of
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 which
is to be used as binder for diamond-abrasive tools be reinforced with 0.01% silicon
nitride (Si3N4). 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 to
e the ability of the matrix to hold the abrasive particles. Without g to be
bound by theory, the inventors e that one reason that metal bonding agents e
the abrasive particles embedded n may be that dislocations inside the metal
g agent weaken the metallic bonding agent. Assuming this theory to be correct,
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 used
for sintering the metal bonding agent. One additive that was tried was aluminum oxide
which was added to an extent corresponding to 1.0 % by volume of the metal bonding
agent. This resulted in a certain ement but the improvement was not as good as
the inventors had hoped. The inventors also tried addition of 0.01 % by volume of
silicon nitride. The improvement of that addition was even less than the ement
achieved by the aluminum oxide.
The inventors then investigated whether increased amounts of silicon nitride would
produce better results. This was confirmed in testes carried out by the inventors. When
silicon nitride was added in quantities significantly larger than 0.01 % by volume of the
metal g agent, it was discovered that a very substantial improvement was
obtained.
For example, the inventors tested a composition in which the metal bonding agent
ned 1.0 % by volume of silicon nitride (Si3N4). A grinding tool with this
ition was then compared to a standard grinding tool using a hybrid matrix and
2012/050842
which did not contain n nitride (Si3N4). The grinding tools were both grinding
wheels in which the abrasive rim 4 was shaped as a ring surrounding the core 2. Under
comparable conditions, the diameter of the standard tool was worn down by 136um
while the diameter of the ng tool with the experimental composition was worn
down by only 58um. The G—ratio for the tool with 1.0 % silicon nitride was 2335. By
ison, a tool using 0.01 % by volume of silicon nitride was worn down 94pm
while a tool using 1.0 % by volume aluminum oxide was worn down 84pm.
A test was made with a composition where silicon nitride constituted 5 % by volume of
the metal bonding agent. The resistance to wear was still good but not quite as good as
for the ng tool with 1.0% by volume silicon nitride. Moreover, the tool with 5.0 %
silicon nitride had higher power consumption. The G—ratio was good but not quite as
good as for the tools with 1.0% and 0.1 % by volume.
The ors have also tested a grinding wheel which had a shape and a composition
similar to the other tools tested but in which the silicon nitride tuted 0.1 % by
volume of the metal bonding agent. It was found that, under the same test conditions as
the other tools that were tested, the wear of the tool with 0.1 % by volume silicon nitride
was 62pm and the G—ration was 2084. While this was inferior to the results obtained at
1 % by volume, it was still a very substantial improvement compared to the standard
grinding tool.
The inventors have also tested a grinding wheel which had a silicon nitride content of
0.02 % by volume of the metal bonding agent but which was otherwise similar to the
other grinding wheels tested. Under similar test conditions, the grinding wheel with 0.02
% by volume of silicon e has a wear (diameter ion) of 58um and a G—ratio of
2283. The results were thus slightly better than the results obtained at a ratio of 0.1 %
by volume.
The results lead to the conclusion that significantly better results are obtained in the
range of 0.02 % - 5.0 % by volume silicon nitride ). In this range, both G—ratio
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 volume,
0.01 % by volume, 0.02 % by volume, 1.0 % by volume and 5.0 % by volume silicon
nitride.
The tools that were tested were grinding wheels of substantially the kind shown in
Figure 5, i.e. grinding tools with an abrasive rim 4 that surrounds a core 2 and where the
grinding tool 1 rotates about the axis A during ion. Resistance to wear as a
function of n nitride content can be seen in Figure 7. The resistance to wear is
expressed in Figure 7 as a resistance to diameter reduction. As can be seen in Figure 7,
resistance to wear increased significantly when the content of silicon nitride was
increased from 0.01 % to 0.02 %. The wear ance continued to be high up to a
silicon nitride content of 5.0 % by volume of the metallic bonding agent. However, at
.0 % by volume silicon nitride, the resistance to wear was somewhat lower compared
to the ance observed at a content of 0.02 % - 1.0 %. The inventors have therefore
concluded that the best wear resistance is obtained in the range of 0.02 % - 5.0 % by
volume.
The G-ratio as a on of silicon nitride content can be seen in Figure 8. As can be
seen in the figure, the best values are ed at a silicon nitride content in the range of
0.02 % - 5.0%. From Figure 8, it can also be derived that the G-ratio is sinking towards
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 contain
silicon e in an amount that constitutes 0.02 % - 5.0 % by volume of the metallic
bonding agent. Since power ption was higher at 5.0 % by volume, the inventors
have concluded that values lower than 5.0% will have good resistance to wear but lower
power consumption compared to tools with a silicon nitride content of 5% by volume.
Therefore, a preferred range may be 0.02 % by volume to 3.0% by volume, 0.5 % - 3.0
% by volume, 0.5 % - 2.0 % by volume or 1.0 % - 2.0 % by volume of the metallic
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 than at
a content of 0.02 % but the power consumption at 5.0 % by volume was more even, the
power consumption was more predictable than at 0.02 % by volume.
The silicon nitride particles should preferably have a size up to 10μm (1250 Tyler
mesh). For sieved particles, this will normally mean that e grain size is less than
10μm. The average le size (D50) of the silicon nitride particles may then be about
2μm - 3μm (depending on how average particle size is measured). The ic e
area of the silicon nitride particles may advantageously be in the range of 5 m2/g – 6
m2/g. If the particles used are too small, this may result in clogging and difficulties
2012/050842
during manufacturing. Moreover, for giving zed strength to the metal bonding
agent, it is believed by the inventors that particles up to lOum should preferably be
included.
Normally, the matrix 6 should further se a polymeric g agent that has been
sintered er with the metallic bonding agent such that the polymeric bonding agent
and the metallic bonding agent form a connected k (even though such a
polymeric bonding agent is optional). The use of a polymeric agent makes it possible to
fine tune the ties of the matrix and adapt it to different kinds of abrasive particles.
The polymeric bonding agent may suitably be polyimide or comprise polyimide. The
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 ric
bonding agent may be present in an amount of up to 50% by volume of the matrix (i.e.
the amount of polymeric bonding agent is in the range of 0% - 50% by volume of the
matrix). For example, the polymeric bonding agent may represent 10 % - 40 % or 10% -
% by volume of the .
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 capable of
withstanding high atures. However, polyimide is preferred since it has better
grinding ties than polyamide-imide.
The metallic bonding agent is a preferably a bronze alloy that comprises copper, tin and
silver. Silver improves the desirable properties of the metal bonding agent.
The abrasive particles 5 may be either diamond particles or cubic boron nitride particles.
Diamonds are harder and have better abrasive properties but cubic boron nitride is more
temperature resistant. Moreover, diamonds may react chemically with certain materials.
The abrasive particles 5 may be are diamond particles or particles of cubic boron
nitride. The particles may be in the range of 4pm - 181 um even though particles outside
this range may be considered depending on the requirements in each specific case. In
many realistic embodiments, the abrasive les 5 may have a mean particle size in
the range of 46pm — 91 um which is a range that is suitable for many grinding
operations.
The abrasive les 5 may optionally have a coating of copper or nickel. A coating of
copper or nickel can improve the bond between the abrasive particles 5 and the matrix
6. However, the abrasive properties of the particles 5 will be somewhat reduced if the
particles have such a coating.
The relative proportion of abrasive particles 5 in relation to the bonding agents and
fillers in the matrix 6 may vary depending on the requirements in each case. In many
realistic embodiments, the amount of abrasive particles may represent a 10 % - 50 % of
the total volume of the abrasive rim (i.e. the total volume of the abrasive particles and
the ). If the relative proportion of ve particles is higher than 50 %, there is a
substantial danger that the matrix will no longer be able to hold the ve particles. If
the relative proportion of abrasive particles is less than 10 %, the grinding effect may
become too small. The relative proportion of abrasive particles may ably be in the
range of 15 % - 30 % and a suitable value may be 25 %.
The silicon nitride is present in the shape of grains having an average grain size which
is equal to or less than 10μm but above 1 μm. For example, they may have a mean size
in the range of 1μm - 10μm or 2μm - 9μm. It is ed by the inventors that n
nitride particles smaller than 0.1μm may result in clogging of the silicon nitride particles
which reduces their reinforcing effect.
The silicon nitride particles may have three different crystallographic ures
designated as α, β and γ phases (also known as trigonal phase, hexagonal phase and
cubic phase). The α 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 be used.
Preferably, the phase used is the α phase. The silicon nitride particles added may also be
a mixture of particles of different .
With reference to Figure 4, a grinding tool according to the invention is compared with
a standard grinding tool. The vertical axis represents power consumption while the
horizontal axis ents number of work pieces upon which the respective grinding
tool has acted. In Figure 4, B5 ents a grinding tool according to the invention
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 nt. The conventional tool as represented by EZ has a power
consumption that rises steeply and then ly drops before it rises again. This
indicates that the abrasive particles of the B5 tool are slowly fragmented while EZ
represents a grinding tool where the abrasive les are suddenly torn away. The wear
on the tool will therefore be faster.
It can be added that B5 represents a tool with both a metal g agent and a
polymeric bonding agent. The metal bonding agent is a bronze that has copper, tin and
silver. It has been sintered using a metal powder that ns 45 % by volume copper,
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 bonding
agent.
The grinding tool of Figure 1 may have a cross section as shown in Figure 5. In such an
embodiment, the abrasive rim 4 is placed radially outside the core 2 such that the rim 4
completely surrounds the core 2. The tests explained with reference to Figure 4, Figure
7 and Figure 8 have been d out on such a grinding tool. However, the invention is
not limited to such an embodiment. With reference to Figure 6, it should be understood
that the core 2 may extend at least as much in the radial direction as the abrasive rim 4.
In Figure 6, the grinding tool has an abrasive rim 4 that does not extend beyond the core
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 of
rotation A of the grinding tool 1 when it is driven by a spindle, see Figure 5 and Figure
6). It should also be understood that the grinding tool 1 is not arily ed for
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 kind of
carrier body for the ve rim. Likewise, the term “rim” should also be understood
broadly as any kind of layer secured to the core 2 such that abrasive particles can act on
a work piece.
The invention further comprises a method of making the ive grinding tool. The
method comprises sintering abrasive les together with metallic powder that
comprises copper and tin such that the sintering results in a matrix in which the abrasive
particles 5 are embedded. The matrix comprises a metallic bonding agent which is a
sintered bronze alloy. According to the invention, silicon nitride in the form of a powder
is added to the metallic powder before sintering to such an extent that the silicon nitride
will constitute 0.1% - 5.0% by volume of the metallic bonding agent.
The metal powder used is preferably metal powder with les that are smaller than
44pm but they should preferably be larger than the silicon nitride particles. Preferably
2012/050842
they should be at least twice as large. An average size in the range of 15um — 44um may
be suitable.
The metallic powder may optionally also comprise silver.
The metal powder may come in the shape of loyed particles or as particles of pure
copper, pure tin, pure silver etc.
A polymer may be added to the metallic powder before sintering, preferably in the form
of polyimide powder, such that also a polymeric bonding agent is formed which is a
part of the matrix 6.
The sintering method may be carried out such that the powder material for the bonding
agents of the matrix 6 is mixed with the abrasive particles 5. The mixture is compacted
in a cold press. Thereafter the compacted is mixture is cured in a kiln at a temperature in
the range of380°C - 520°C, preferably 400°C - 500°C or 440°C - 460°C, for a period of
120 — 150 s. The time required depends on size. In a larger press form, more time
is required. Thereafter (preferably immediately thereafter) the compacted and cured
mixture is placed in a press and subjected to a pressure of 1500 — 2000 kg/cmz‘ The
pressure is then maintained until the mixture has reached a temperature below 300°C.
For example, the ors have made ng tools according to this method in a
process where the ature in the kiln was 450°C.
The ve 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 ve particles may be sintered separately and
subsequently fastened (e. g. glued) onto the core 2. Alternatively, the abrasive rim 5 may
be sintered directly onto the core 2 such that it is bonded to the core as it is formed.
Before sintering, the core 2 may be electrolytically plated with copper on at least one
surface of the core which will meet the abrasive rim 4. The abrasive rim 4 can then be
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 abrasive
particles 5 before the sintering operation. As previously explained, the filler material
may comprise graphite. Other possible filler als 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 /Co), copper — tin — nickel
(Cu/Sn/Ni) or copper — tin — silver (Cu/Sn/Ag). Even more preferred, the bronze is a
copper — tin — silver bronze. Other bronze alloys can also be considered.
The inventive grinding tool can be used for machining hard and/or brittle materials.
This does not exclude the ility that the grinding tool can be used also for other
materials.
In embodiments of the ion, the matrix 6 may optionally also comprise at least one
ceramic component in the shape of ceramic particles. The c component may be,
for example, frit and contain SlOz. c particles for the matrix may be frit in the
shape of cal particles having a particle size of 50pm - SOOum depending on the
size of the abrasive particles. For larger abrasive particles, larger ceramic particles will
be used. The abrasive particles may be embedded in the ceramic particles while the
ceramic particles are embedded in a hybrid matrix with a ic bonding agent and a
polymeric bonding agent. The ceramic particles may be held stronger by the matrix than
the abrasive particles would be held. The free-cutting properties of the abrasive rim are
thus improved. The ceramic component does not have such a good resistance to wear as
the metallic g agent. By combining ceramics, metal and polymeric bonding
agents, it is possible to combine the best properties of these bonding agents.
Claims (24)
1. A grinding tool for machining hard and/or brittle materials which grinding tool comprises a core and an abrasive rim, the abrasive rim comprising ve les embedded in a matrix, the matrix comprising a metallic bonding agent which is 5 a sintered bronze alloy, the metallic bonding agent tuting 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 of the metallic bonding agent characterized in that the silicon nitride is present in the shape of grains having an average grain size which is n 1 µm and 10μm. 10
2. A grinding tool according to claim 1, wherein the silicon nitride is crystalline.
3. A grinding tool according to claim 1 or claim 2, wherein the matrix further comprises a polymeric bonding agent that has been sintered together with the metallic bonding agent such that the polymeric bonding agent and the metallic bonding agent 15 form a connected network.
4. A grinding tool according to any one of claims 1 – 3, wherein the silicon e constitutes 0.3 % - 5.0 % by volume of the metallic bonding agent.
5. A ng tool according to any one of claims 1 – 4, wherein the silicon nitride constitutes 0.5 % - 3 % by volume of the metallic bonding agent. 20
6. A grinding tool according to any one of claims 1 – 5, wherein the silicon nitride constitutes 0.5 % - 2 % by volume of the ic bonding agent.
7. A ng tool according to claim 3, wherein the polymeric bonding agent comprises polyimide.
8. A grinding tool according to any one of claims 1 – 3, wherein the matrix 25 additionally comprises filler materials.
9. A grinding tool according to claim 8, n the filler material is graphite.
10. A grinding tool according to any one of claims 1 – 9, wherein the ic bonding agent is a bronze alloy that comprises copper, tin and silver. 30
11. A grinding tool according to any one of claims 1 – 10, wherein the abrasive particles are diamond particles or cubic boron nitride particles.
12. A grinding tool according to claim 11, wherein the abrasive particles have a mean particle size in the range of 4μm - 181μm.
13. A grinding tool ing to claim 11 or 12, wherein the abrasive particles have a mean particle size in the range of 46μm – 91μm. 5
14. A grinding tool according to claim 12 or claim 13, wherein the ve particles have a coating of copper or nickel.
15. A method of making a grinding tool comprising a core and an abrasive rim, which method comprises ing abrasive particles together with metallic powder that comprises copper and tin such that the sintering results in a matrix in which the 10 abrasive particles are embedded, the 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 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 wherein the silicon nitride which is added is in the shape of grains having an average 15 grain size which is between 1 µm and 10μm.
16. A method ing to claim 15, n the silicon nitride is crystalline.
17. A method according to claim 15 or claim 16, wherein the metallic powder additionally comprises silver.
18. A method according to any one of claims 15 – 17, wherein a polymer is 20 added to the metallic powder before sintering.
19. A method ing to claim 18, wherein the polymer is in the form of ide powder, such that also a polymeric bonding agent is formed which is a part of the matrix.
20. A method ing to any one of claims 15 – 19, wherein the method 25 comprises; mixing the powder material for the bonding agents of the matrix with the abrasive particles; compacting the mixture in a cold press; curing the compacted mixture in a kiln at a temperature in the range of 380°C - 520°C, for a period of 120 – 150 minutes; thereafter placing the compacted and cured e in a press and subjecting it to a pressure of 1500 – 2000 kg/cm2; and holding the pressure until the 30 mixture has reached a temperature below 300°C.
21. A method according to claim 20, n the compacted mixture is cured at a temperature in the range of 400°C - 500°C.
22. A method according to any one of claims 15 – 21, n filler material is added to the mixture of metallic powder and abrasive particles before the sintering operation and wherein the filler material comprises graphite.
23. A grinding tool substantially as herein described or exemplified, with 5 reference to the accompanying gs.
24. A method according to claim 15, substantially as herein described or exemplified.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE1150720A SE537723C2 (en) | 2011-07-22 | 2011-07-22 | A grinding tool for machining brittle materials and a process for making a grinding tool |
| SE1150720-9 | 2011-07-22 | ||
| PCT/SE2012/050842 WO2013015737A1 (en) | 2011-07-22 | 2012-07-18 | A grinding tool for machining brittle materials and a method of making a grinding tool |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ620302A NZ620302A (en) | 2015-12-24 |
| NZ620302B2 true NZ620302B2 (en) | 2016-03-30 |
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