BACKGROUND
[0001] Bonded abrasive articles have abrasive particles bonded together by a bonding medium.
There is an increasing demand for high-performance abrasive articles such as grinding
wheels that abrade material faster while meeting tight tolerances without damaging
workpieces.
[0002] Abrasive articles such as stones, hones and wheels may be driven by a stationary-mounted
motor such as, for example, a bench grinder, or attached and driven by a hand-operated
portable grinder. Hand-operated portable grinders are typically held at a slight angle
relative to the surface of the workpiece, and may be used to grind, for example, welding
beads, flash, gates, and risers off castings.
WO 2009/039381 A1 describes abrasive products, which in one form are bonded abrasive products that
include a plurality of abrasive powders bonded together by a resin binder.
SUMMARY
[0003] Disposing a grinding layer at a surface of or within the interior of a bonded abrasive
article was found to surprisingly enhance cutting and grinding performance compared
to conventional bonded discs. In particular, among other advantages, the total cut
surprisingly increased.
[0004] In one aspect, the present disclosure provides a bonded abrasive article comprising
a matrix and a grinding layer. The matrix comprises matrix abrasive particles and
a matrix binder. The grinding layer comprises erectly-oriented abrasive particles
and a grinding layer binder. The grinding layer is disposed on an exterior surface
of the bonded abrasive article or is disposed at least partly within the interior
of the bonded abrasive article. In another aspect, the present disclosure provides
a method of forming a bonded abrasive article, the method comprising: applying a matrix
mixture to a grinding layer, the matrix mixture comprising a curable matrix binder
and matrix abrasive particles, the grinding layer comprising erectly-oriented grinding
abrasive particles; and curing the matrix binder (14).
[0005] In yet another aspect, the present disclosure provides a method of forming a bonded
abrasive article, the method comprising applying a grinding layer precursor to a first
major surface of a matrix, the matrix comprising matrix abrasive particles and a matrix
binder; depositing erectly-oriented particles on the grinding layer precursor, applying
a sizing layer on the erectly-oriented particles, and curing the grinding layer precursor
to form a grinding layer attached to the first major surface.
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] Repeated use of reference characters in the specification and drawings is intended
to represent the same or analogous features or elements of the disclosure.
FIG. 1A is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment.
FIG. 1B is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment.
FIG. 2 is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment.
FIG. 3 is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment.
FIG. 4A is a schematic view of apparatus for erectly orienting abrasive particles.
FIG. 4B is a schematic cross-sectional view of an abrasive article with erectly-oriented
abrasive particles.
FIG. 5A is a schematic top view of an article with erectly-oriented abrasive particles.
FIG. 5B is a schematic method of forming a bonded abrasive article according to an embodiment.
FIG. 5C is a perspective view of a bonded abrasive article according to an embodiment.
FIG. 5D is a perspective view of a bonded abrasive article according to an embodiment.
DEFINITIONS
[0007] "Bonded abrasive articles" are abrasive articles having bonded abrasives, including,
without limitation, grinding wheels, grinding discs, grinding cylinders or abrasive
articles in any other forms.
[0008] While the above-identified drawing figures set forth several embodiments of the present
disclosure, other embodiments are also contemplated, as noted in the discussion. The
figures may not be drawn to scale. Like reference numbers may have been used throughout
the figures to denote like parts.
DETAILED DESCRIPTION
[0009] Referring now to
FIG. 1A, an exemplary bonded abrasive article
10 according to one embodiment has a matrix
13 and a grinding layer
16. The matrix
13 has two major opposing surfaces: a first major surface
21, and a second major surface
23. The grinding layer
16 has two opposing faces, a grinding face
19 and a back face
17. The grinding face
19 comprises the distal tips of the erectly-oriented abrasive particles
18 and may be uneven or undulating depending on the abrasive particles employed. The
back face
17 is typically substantially planar replicating, in one embodiment, the planar support
surface the erectly-oriented abrasive particles are applied to. In an embodiment,
the grinding layer
16 is disposed on the first major surface
21 or the second major surface
23 such that the back face
17 is proximal to the matrix
13 while the grinding face
19 is distal to the matrix
13.
[0010] The matrix
13 includes matrix abrasive particles
12 and a matrix binder
14. The matrix
13 may be shaped like a disc, a wheel, a cylinder or any other suitable shape known
in the art. The matrix
13 may have openings, including central openings, such as central holes. The matrix
13 may have a depressed center with a central hole. The matrix
13 may have a backing, including paper, fabric, or film backings, or any other backing
known in the art or described below or combinations thereof.
[0011] The matrix binder
14 holds the matrix abrasive particles
13 in a fixed configuration within the matrix
13 and provides a rigid structure to the matrix
13. The matrix binder
14 may contain any suitable organic, resin, metallic, vitrified or any other binder
known in the art such as binders described below or combinations thereof.
[0012] The matrix abrasive particles
12 may be any abrasive particles known in the art, including conventional crushed abrasive
particles, shaped abrasive particles, or any abrasive particles described below or
their combinations thereof. The matrix abrasive particles
12 may be randomly dispersed within the matrix
14, or may be dispersed in a predetermined pattern within the matrix
14. The matrix abrasive particles
12 may be randomly oriented within the matrix
14, or may be oriented in predetermined orientations within the matrix
14. Some, all or none of the matrix abrasive particles
12 may be oriented in substantially similar or parallel orientations within the matrix
13. Some, all, or none of the matrix abrasive particles
12 may be of substantially same, similar or different sizes. Some, all, or none of the
matrix abrasive particles
12 may have substantially same, similar or different shapes. The matrix abrasive particles
12 can contain abrasive particles of the same or different chemical compositions, with
the same, similar, dissimilar or different chemical and physical properties such as
electrostatic attraction, hardness, and fracture toughness. Some, all or none of the
matrix abrasive particles
12 may be completely immersed within the matrix
14. Some or all of the matrix abrasive particles
12 may be incompletely immersed within the matrix
14. The matrix abrasive particles
12 abrade surfaces to a varying extent, such as low abrasion, medium abrasion, high
abrasion or any other known abrasive extent, depending on factors such as size, geometry,
orientation and material of the matrix abrasive particles
12, and factors such as the pressure and speed at which surfaces are exposed to the matrix
13.
[0013] The grinding layer
16 contains erectly-oriented abrasive particles
18 bonded and held in an erectly-oriented configuration by a grinding layer binder
20. In an embodiment, the grinding layer
16 also contains abrasive particles that are not erectly-oriented. In an embodiment,
the grinding layer
16 has a thickness that is less than the thickness of the matrix
13. In an embodiment, the grinding layer
16 has a thickness that is 95%, or 90%, or 85%, or 80%, or 75%, or 70%, or 65% or 60%
or 55% or 50% or any other percentage that is less than 100% but greater than 0% of
the thickness of the matrix
13. In another embodiment, the grinding layer binder
20 is sufficiently thick that all the erectly-oriented particles are immersed within
the grinding layer
16. In yet another embodiment, the grinding layer binder
20 has a thickness that is less than the height of the erectly-oriented particles
18 such that the erectly-oriented particles
18 at least partially protrude from the exposed surface of the grinding layer binder
20.
[0014] The grinding layer
16 may optionally be bonded to the matrix
13 by an adhesive. The grinding layer
16 may optionally be bonded to the matrix
13 by the grinding layer binder
20. The grinding layer
16 may be optionally bonded to the matrix
13 by an additional binder layer containing any suitable binder known in the art, including
any one or more suitable binders described below, including organic, resin, metallic,
or vitrified binders.
[0015] The grinding layer binder
20 holds the erectly-oriented abrasive particles
18 in a fixed configuration within the grinding layer
16. The grinding layer binder
20 may contain any suitable organic, resin, metallic, vitrified or any other binder
known in the art such as binders described below or those used in make coats or combinations
thereof. The grinding layer binder
20 can be formed by coating a curable grinding layer precursor onto a major surface
of the matrix
13. The grinding layer precursor refers to coatable materials applied to the matrix
13 which can be hardened, for instance, by curing, to form the grinding layer
16. The grinding layer binder
20 can also be formed by coating a grinding layer precursor onto any other suitable
holding surface that can be used to assemble the grinding layer
16. The grinding layer precursor or the grinding layer binder
20 may comprise, for example, glue, phenolic resin, aminoplast resin, urea-formaldehyde
resin, melamine-formaldehyde resin, urethane resin, free-radically polymerizable polyfunctional
(meth)acrylate (e.g., aminoplast resin having pendant alpha,beta-unsaturated groups,
acrylated urethane, acrylated epoxy, acrylated isocyanurate), epoxy resin (including
bis-maleimide and fluorene-modified epoxy resins), isocyanurate resin, and any binder
described below or mixtures thereof.
[0016] Erectly-oriented abrasive particles
18 are abrasive particles having a predetermined axis that is erectly-oriented with
respect to the grinding layer
16. The predetermined axis can be any geometric axis passing through the article. In
an embodiment, the predetermined axis is the longest axis passing through each of
the erectly-oriented abrasive particles
18. In another embodiment, the predetermined axis is the shortest axis passing through
each of the erectly-oriented abrasive particles
18. In yet another embodiment, the predetermined axis is the axis that passes through
a sharp abrasive vertex of each of the erectly-oriented abrasive particles
18. In a further embodiment, the predetermined axis passes through the center of mass
of each of the erectly-oriented abrasive particles
18. In still other embodiments, the predetermined axis is any other geometric axis.
[0017] Erectly-oriented abrasive particles
18 include particles with a predetermined axis that can assume any suitable angle ranging
from, without limitation, 30° to 90° with respect to the grinding layer
16. For instance, in an embodiment, the predetermined axis is substantially normal to
the grinding layer
16. A substantially perpendicular or normal predetermined axis has an angle that is close
to 90° or is a right angle within a predetermined tolerance with respect to the grinding
layer
16. In another embodiment, the predetermined axis assumes non-perpendicular angles that
are less than 90°, for instance, any angle within the range of, without limitation,
30° to 89°.
[0018] In an embodiment, erectly-oriented abrasive particles
18 include abrasive particles that have at least one vertex that is elevated with respect
to the grinding layer erectly-oriented abrasive particles
18 include abrasive particles. In another embodiment, erectly-oriented abrasive particles
18 include abrasive particles that have at least one vertex that protrudes from the
grinding layer
16. A vertex is any geometric vertex such as a tip, an end, a point, a protrusion or
any other geometric vertex of an abrasive particle.
[0019] In an embodiment, all of the abrasive particles in the grinding layer
16 are erectly-oriented abrasive particles
18. In another embodiment, at least 10% by weight of the abrasive particles in the grinding
layer are erectly-oriented abrasive particles
18. In yet another embodiment, at least 20% by weight, or at least 30% by weight, or
at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at
least 70% by weight, or at least 80% by weight, or at least 90% by weight of the abrasive
particles are erectly-oriented abrasive particles. In other embodiments, the abrasive
particles in the grinding layer contain any amount, ranging from 10% to 100% by weight,
of erectly-oriented abrasive particles
18.
[0020] The erectly-oriented particles
18 can comprise shaped abrasive particles or formed abrasive particles. In an embodiment,
the shaped abrasive particles have polygonal faces and a polygonal base. In another
embodiment, the shaped abrasive particles have a triangular face and a trapezoidal
base. In other embodiments, the erectly-oriented abrasive particles
18 contain other abrasive particles known in the art, including conventional crushed
abrasive particles, shaped abrasive particles, or any abrasive particles described
below or their combinations thereof, disposed in the grinding layer
16 such that a predetermined axis of the particles is erectly-oriented. In one embodiment,
the predetermined axis is perpendicular to one side of a triangular shaped abrasive
particle and extends through the opposing vertex or tip of the triangular shaped abrasive
particle such that the erectly-orientated abrasive particles are positioned as shown
in
FIG. 1A.
[0021] Abrasive particles can include shaped, fractured abrasive particles, as disclosed
in
U.S. Pat. No. 8,034,137; abrasive shards, shaped abrasive particles with openings, or dish shaped abrasive
articles as disclosed in
U.S. Pat. No. 8,123,828; dish-shaped abrasive particles with a recessed surface as disclosed in
U.S. Pat. No. 8,142,891; shaped abrasive particles with an opening as disclosed in
U.S. Pat. No. 8,142,532; shaped abrasive particles with grooves as disclosed in published
U.S. Pat. Application No. 2010/0146867; shaped abrasive particles with a sloping sidewall as disclosed in
U.S. Pat. No. 8,142,531; shaped abrasive particles with low roundness factor as disclosed in published
U.S. Pat. Application No. 2010/0319269; dual tapered shaped abrasive particles as disclosed in P.C.T. Application No.
PCT/US2010/057713; and shaped abrasive particles disclosed in published
U.S. Pat. Application No. 2011/0146509.
[0022] The erectly-oriented abrasive particles
18 may be randomly dispersed across the grinding layer
16, or may be dispersed in a predetermined pattern across the grinding layer
16. The erectly-oriented particles
18 may be oriented in different orientations across the grinding layer
16 such that even though each of the erectly-oriented particles
18 is substantially erectly-oriented, each of the erectly-oriented particles
18 assumes different orientations. Some, all or none of the erectly-oriented abrasive
particles
16 may be oriented in a substantially similar or parallel orientation across the grinding
layer
16. Some, all, or none of the erectly-oriented abrasive particles
18 may be of substantially the same, similar or different sizes. Some, all, or none
of the erectly-oriented abrasive particles
18 may have substantially same, similar or different shapes. The erectly-oriented abrasive
particles
18 can contain abrasive particles of the same or different chemical compositions, with
the same, similar, dissimilar or different chemical and physical properties such as
electrostatic attraction, hardness, and fracture toughness. The erectly-oriented abrasive
particles
18 may abrade surfaces to varying extents, such as low abrasion, medium abrasion, high
abrasion or any other known abrasive extent, depending on factors such as size, geometry,
orientation and composition of the erectly-oriented abrasive particles
18, and factors such as the pressure and speed at which surfaces are exposed to the
grinding layer
16 containing the erectly-oriented abrasive particles
18.
[0023] The matrix binder
14 and the grinding layer binder
20 may be the same or different (chemically or physically different). For example, the
matrix binder
14 can be a first phenolic binder and the grinding layer binder
20 can be a second phenolic binder that is different from the first phenolic binder.
[0024] In an embodiment, an optional size layer
22 is optionally coated over the erectly-oriented particles
18 at the surface of the grinding layer
16. The size layer
22 may be coated by any conventional technique, such as knife coating, spray coating,
roll coating, curtain coating, rotogravure coating, and the like. The size layer
22 maintains the integrity of the grinding layer 16, including the erectly-oriented
abrasive particles
18. The size layer
22 may contain any suitable organic, resin, metallic, vitrified or any other sizing
agent or binder known in the art such as binders described below or those used in
sizing coats or combinations thereof. The size layer
22 can be formed by coating a curable size layer precursor onto the exposed surface
of the grinding layer
16. The size layer precursor refers to coatable materials applied to the grinding layer
16, for example, over the top of the erectly-oriented abrasive particles
18. The size layer precursor can be hardened, for instance, by curing, to form the size
layer
22. The size layer precursor or the size layer binder
20 may comprise, for example, glue, phenolic resin, aminoplast resin, urea-formaldehyde
resin, melamine-formaldehyde resin, urethane resin, free-radically polymerizable polyfunctional
(meth)acrylate (e.g., aminoplast resin having pendant alpha,beta-unsaturated groups,
acrylated urethane, acrylated epoxy, acrylated isocyanurate), epoxy resin (including
bis-maleimide and fluorene-modified epoxy resins), isocyanurate resin, or any binder
described below or mixtures thereof.
[0025] The matrix binder
14, the grinding layer binder
20, or the size layer
22 can each further comprise additives known in the art, such as, for example, fillers,
grinding aids, wetting agents, surfactants, dyes, pigments, coupling agents, or any
other additives described herein and combinations thereof.
[0026] In an embodiment, the matrix
13 is a disc having a diameter of 7 inches with a central hole of diameter 7/8 inch.
The grinding layer
16 is disposed on one of the major surfaces of the matrix
13. The combined thickness of the matrix
13 and the grinding layer
16 is 1/8 inch. Thus the bonded abrasive article is of diameter 7 inches, with a central
hole of diameter 7/8 inch. The bonded abrasive article can have a depressed central
region, for instance, as in a type 27 disc.
[0027] FIG. 1B is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment. The bonded abrasive article comprises a matrix
14 and a grinding layer
16. The matrix
14 is described above. Though
FIG. 1B represents an embodiment in which the grinding layer
16 comprises erectly-oriented abrasive particles
18 comprising crushed abrasive particles, the erectly-oriented abrasive particles
18 can be any erectly-oriented abrasive particles
18 as described herein.
[0028] In an embodiment, the grinding layer
16 further optionally comprises a backing
24. The backing
24 may be disposed at the back face
17 of the grinding layer
16, such that the backing
24 is disposed between the matrix
13 and the back face
17. The backing
24 may be continuous, for instance, extending continuously across the bottom unexposed
surface between the grinding layer
16 and the matrix
13. The backing
24 may be discontinuous, for instance, extending in regular or irregular patterns or
patches across the bottom unexposed surface between the grinding layer
16 and the matrix
13. The backing
24 helps in retaining the configuration of the grinding layer
16, the grinding layer binder
18, and the erectly-oriented abrasive particles
18. The backing
24 may comprise any backing known in the art, including paper, fabric, or film backings,
or any other backing known in the art or described below or combinations thereof.
In another embodiment, the backing
24 can comprise a scrim material such as an open weave woven or knitted material to
which the erectly-oriented abrasive particles are applied. The scrim backing for the
grinding layer
16 can also be used to reinforce the matrix
14; especially, when the grinding layer
16 is primarily disposed within the matrix
14.
[0029] In an embodiment, the grinding layer
16 comprises the backing
24, the grinding layer binder
20, erectly-oriented abrasive particles
18, and the size layer
22. In another embodiment, the grinding layer
16 comprises a coated abrasive article comprising the backing
24, the grinding layer binder
20, erectly-oriented abrasive particles
18, and the size layer
22.
[0030] The grinding layer
16 is optionally attached to the matrix by an adhesive layer
26. In an embodiment, the grinding layer
16 comprises the adhesive layer
26. In another embodiment, the grinding layer
16 comprises both the backing 24 and the adhesive layer
26. In yet another embodiment, the grinding layer
16 comprises an abrasive article and the adhesive layer
26, the abrasive article comprising the backing
24, the grinding layer binder
20, erectly-oriented abrasive particles
18, and the size layer
22, wherein the adhesive layer
26 is disposed between the backing
24 and the matrix
13.
[0031] The adhesive layer
26 can comprise any adhesive known in the art, including but not limited to pressure
sensitive adhesives, curable epoxies, phenolics, resins, silicones, acrylics, and
styrene-butadiene copolymers or combinations thereof.
[0032] FIG. 2 is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment. The grinding layer
16 is disposed on a second major surface
23 of the matrix
13, such that the matrix covers the grinding layer
16. The grinding face
19 is proximal to the matrix
13 while the back face
17 of the grinding layer
16 is distal to the matrix
13. In an embodiment, the grinding layer
16 comprises the optional sizing layer
22 described herein. In another embodiment, the grinding layer
16 comprises the optional backing
24 described herein.
[0033] In an embodiment, the grinding layer
16 is disposed partly within the interior of the matrix
13, such that the matrix
13 covers at least a portion of the grinding face
19. In another embodiment, the grinding layer
16 is disposed completely within the interior of the matrix
13 such that the matrix
13 substantially covers the grinding face
19.
[0034] FIG. 3 is a schematic cross-sectional view of a bonded abrasive article according to an
embodiment. In an embodiment, the bonded abrasive article comprises a matrix 13, a
first grinding layer
16' and a second grinding layer
16" The first grinding layer
16' comprises erectly-oriented abrasive particles
18' and a grinding layer binder
20'. The second grinding layer
16" comprises erectly-oriented abrasive particles
18" and a grinding layer binder
20". The first grinding layer
16' has a grinding face
19' and a back face
17'. The second grinding layer
16" has a grinding face
19" and a back face
17". The first grinding layer
16' is disposed at a first major surface
21 of the matrix such that the back face
17' of the first grinding layer
16' is proximal to the matrix
13 and the grinding face
19' is distal to the matrix
13. The second grinding layer
16" is disposed at a second major surface
23 of the matrix such that the back face
17" of the second grinding layer
16" is distal to the matrix
13 and the grinding face
19" is proximal to the matrix
13. The matrix
13 covers the grinding face
19" of the second grinding layer
16". The second grinding layer
16" comprises the backing
24".
[0035] In an embodiment, the back face
17' of the first grinding layer
16' is bonded to the matrix
13. In another embodiment, the first grinding layer
16' comprises a backing
24 and the matrix
13 is bonded to the backing
24. In yet another embodiment, the first grinding layer
16' comprises a backing
24 and an adhesive layer
26 and the matrix
13 is bonded to the backing
24 by the adhesive layer
26.
[0036] In an embodiment, multiple grinding layers
16 are disposed such that some, all or none of the multiple grinding layers
16 are disposed at the surface of matrix
13, some, all or none of the multiple grinding layers
16 are disposed partly within the interior of matrix
13, and some, all or none of the multiple grinding layers
16 are disposed completely within the interior of matrix
13.
[0037] FIG. 4A is a schematic view of apparatus for erectly-orienting abrasive particles. In an
embodiment, a method of forming a bonded abrasive articles comprises electrostatically
erectly-orienting the abrasive particles
18'. Abrasive particles
18' are distributed on a first support
28. A grinding layer binder precursor
20' is coated on the first major surface
21 of the matrix
13. In an embodiment, the grinding layer binder precursor
20' is coated on the second major surface
23 of the matrix
13. The coated major surface is maintained proximal to the abrasive particles
18'. An electrostatic field is applied between the first support
28 and the matrix
13. The electrostatic field erectly-orients the abrasive particles
18' and causes them to be attracted towards the matrix
13 such that the abrasive particles
18' attach to the coating of the grinding layer binder precursor
20' while maintaining an erectly-oriented configuration.
[0038] The electrostatic field can be generated using any known electrostatic field generating
apparatus known in the art. For example, a useful electrostatic field generating apparatus
includes electrodes having an electrical potential applied between them with one electrode
placed above the matrix
13 and the opposing electrode placed below the first support
28. The electrical potential can be supplied by a suitable A.C. or D.C. power supply.
In an embodiment, shaped electrodes are used to apply the abrasive grains
18' in a predetermined pattern, for example, as disclosed in
U.S. Pat. No. 6,511,713.
[0039] In an embodiment, the first support
28 is stationary. In another embodiment, the first support
28 comprises a moving belt or surface. In an embodiment, the matrix
13 is stationary. In another embodiment, the matrix
13 is moved as the abrasive particles
18' are electrostatically attracted towards the matrix
13. In various embodiments, at least some, or a majority, or substantially all, of the
abrasive particles
18' are attracted to the matrix
13 and attach to the coating of the grinding layer precursor
20'.
[0040] FIG. 4B is a schematic cross-sectional view of an abrasive article with erectly-oriented
abrasive particles. The abrasive particles
18', having being attracted to the matrix
13 by the electrostatic field, form erectly-oriented abrasive particles
18 on the coating of the grinding layer binder precursor
20' on one of the major surfaces
21 and
23 of the matrix
13.
[0041] In an embodiment, the grinding layer binder precursor
20' is hardened, for example, by curing, after the abrasive particles
18' have been attached, while retaining their erectly-oriented configuration, to form
the cured grinding layer binder
20 with erectly-oriented abrasive particles
18. In another embodiment, the grinding layer binder precursor
20' is partially cured before abrasive particles
18' are attached to it, and completely cured after the abrasive particles
18' are attached.
[0042] FIGS. 5A, 5B, 5C and
5D show a method for preparing a bonded abrasive article according to an embodiment.
FIG. 5A is a schematic perspective view of an abrasive article
32 prior to the application of a matrix
13. The abrasive article
32 comprises a grinding layer
16, and erectly-oriented abrasive particles
18. The abrasive article
32 is shaped in the form of a disc, and has a mounting hole
30. In an embodiment, the abrasive article
32 is shaped to conform to the shape of a type
27 grinding wheel. In another embodiment, the abrasive article
32 is shaped in the form of a disc with a diameter of 7 inches and a central hole of
diameter 7/8 inch. In an embodiment, the abrasive article comprises optional backing
24. In another embodiment, the abrasive article comprises optional sizing layer
22.
[0043] FIG. 5B is a cross-sectional view of matrix precursor
13' being applied to the abrasive article
32. The abrasive article
32 comprises a grinding layer
16. The grinding layer
16 comprises a grinding layer binder
20. Matrix precursor
13' is applied to the grinding face of the abrasive article
32. Matrix precursor
13' comprises curable matrix binder
14' and matrix abrasive particles
12. A predetermined amount of the matrix precursor
13' can be applied to the surface of the abrasive article
32 by any method known in the art, including, without limitation, spreading, coating,
dispersing or combinations thereof.
[0044] FIG. 5C is a cross-sectional view of matrix precursor
13' being applied to the abrasive article
32. The abrasive article
32 comprises a grinding layer
16. The grinding layer
16 comprises a grinding layer binder
20. Applied matrix precursor
13' is settling and the curable matrix binder
14' is being cured to form the matrix binder
14. Matrix precursor
13' comprises curable matrix binder
14' and matrix abrasive particles
12. In an embodiment, the matrix precursor
13' condenses slightly on curing, so that the thickness of the matrix precursor
13' comprising curable matrix binder
14' is greater than the thickness of the matrix
13 comprising cured matrix binder
14.
[0045] FIG. 5D is a perspective view of a bonded abrasive article according to an embodiment, after
applying and curing a matrix precursor. Abrasive article
32 comprises a grinding layer
16, erectly-oriented abrasive particles
18, and a matrix
13. Matrix
13 is formed on the grinding face of the abrasive article
32 by curing the curable matrix binder
14' in the matrix precursor
13'. The erectly-oriented abrasive particles
18 retain their original configuration. The matrix
13 is bonded to the grinding face
19 of the grinding layer
16 in the abrasive article
32.
[0046] Abrasive particles, binders, fillers, backings, grinding aids and other additives
that can be used in various embodiments are described below.
Abrasive Particles
[0047] Useful abrasive particles include conventional abrasive particles including any abrasive
particles known in the abrasive art. Exemplary useful abrasive particles include fused
aluminum oxide based materials such as aluminum oxide, ceramic aluminum oxide (which
may include one or more metal oxide modifiers and/or seeding or nucleating agents),
and heat-treated aluminum oxide, silicon carbide, black silicon carbide, green silicon
carbide, co-fused alumina-zirconia, diamond, ceria, titanium diboride, cubic boron
nitride, boron carbide, garnet, flint, emery, sol-gel derived abrasive particles,
and mixtures thereof. The abrasive particles may be in the form of, for example, individual
particles, agglomerates, composite particles, and mixtures thereof.
[0048] Useful crushed abrasive particles include, for example, crushed particles of fused
aluminum oxide, white fused aluminum oxide, ceramic aluminum oxide materials such
as those commercially available under the trade designation 3M CERAMIC ABRASIVE GRAIN
from 3M Company of St. Paul, Minnesota, titanium diboride, tungsten carbide, titanium
carbide, sol-gel derived abrasive particles, iron oxide, chromia, zirconia, titania,
silicates, tin oxide, silica (such as quartz, glass beads, glass bubbles and glass
fibers) silicates (such as talc, clays (e.g., montmorillonite), feldspar, mica, calcium
silicate, calcium metasilicate, sodium aluminosilicate, sodium silicate). Examples
of sol-gel derived abrasive particles can be found in
U.S. Patent Nos. 4,314,827 (Leitheiser et al),
4,623,364 (Cottringer et al);
4,744,802 (Schwabel),
4,770,671 (Monroe et al.); and
4,881,951 (Monroe et al.). It is also contemplated that the abrasive particles could comprise abrasive agglomerates
such, for example, as those described in
U.S. Patent Nos. 4,652,275 (Bloecher et al.) or
4,799,939 (Bloecher et al).
[0049] The abrasive particles may, for example, have an average diameter of at least about
0.1 micrometer, at least about 1 micrometer, or at least about 10 micrometers, and
less than about 10,000 micrometers, or less than about 8,000 micrometers, or less
than about 5,000 micrometers, although larger and smaller abrasive particles may also
be used. For example, the conventional abrasive particles may have an abrasives industry
specified nominal grade. Such abrasives industry accepted grading standards include
those known as the American National Standards Institute, Inc. (ANSI) standards, Federation
of European Producers of Abrasive Products (FEPA) standards, and Japanese Industrial
Standard (JIS) standards. Exemplary ANSI grade designations (i.e., specified nominal
grades) include: ANSI 12 (1842 µm), ANSI 16 (1320 µm), ANSI 20 (905 µm), ANSI 24 (728
µm), ANSI 36 (530 µm), ANSI 40 (420 µm), ANSI 50 (351 µm), ANSI 60 (264 µm), ANSI
80 (195 µm), ANSI 100 (141 µm), ANSI 120 (116 µm), ANSI 150 (93 µm), ANSI 180 (78
µm), ANSI 220 (66 µm), ANSI 240 (53 µm), ANSI 280 (44 µm), ANSI 320 (46 µm), ANSI
360 (30 µm), ANSI 400 (24 µm), and ANSI 600 (16 µm). Exemplary FEPA grade designations
include P12 (1746 µm), P16 (1320 µm), P20 (984 µm), P24 (728 µm), P30 (630 µm), P36
(530 µm), P40 (420 µm), P50 (326 µm), P60 (264 µm), P80 (195 µm), P100 (156 µm), P120
(127 µm), P120 (127 µm), P150 (97 µm), P180 (78 µm), P220 (66 µm), P240 (60 µm), P280
(53 µm), P320 (46 µm), P360 (41 µm), P400 (36 µm), P500 (30 µm), P600 (26 µm), and
P800 (22 µm). An approximate average particles size of reach grade is listed in parenthesis
following each grade designation.
[0050] Useful abrasive particles also include formed ceramic abrasive particles and, in
particular, shaped abrasive particles. Shaped abrasive particles can be prepared according
to the disclosures of
U.S. 8,142,531. The shaped abrasive particles were prepared by shaping alumina sol gel from, for
example, equilateral triangle-shaped polypropylene mold cavities of side length 0.031
inch (0.79 mm) and a mold depth of 0.008 inch (0.2 mm). After drying and firing, such
resulting shaped abrasive particles comprised triangular plates that were about 280
micrometers (longest dimension) and would pass through a 50-mesh sieve and be retained
upon a 60-mesh sieve. In one embodiment, the triangular shaped abrasive particles
comprise a first face, an opposing second face connected to the first face by a sidewall
where the perimeter of each face is a triangular and desirably an equilateral triangle.
In some embodiments, the sidewall, instead of having a 90 degree angle to both faces,
is a sloping sidewall as disclosed in
US 8,142,531 having a draft angle α between the second face and the sloping sidewall between about
95 degrees to about 130 degrees, which has been determined to greater enhance the
cut rate of the triangular shaped abrasive particles.
[0051] As used herein "formed ceramic abrasive particle" means an abrasive particle having
at least a partially replicated shape. One process to make a formed ceramic abrasive
particle includes shaping the precursor ceramic abrasive particle in a mold having
a predetermined shape to make ceramic shaped abrasive particles. Ceramic shaped abrasive
particles, formed in a mold, are one species in the genus of formed ceramic abrasive
particles. Other processes to make other species of formed ceramic abrasive particles
include extruding the precursor ceramic abrasive particle through an orifice having
a predetermined shape, printing the precursor ceramic abrasive particle though an
opening in a printing screen having a predetermined shape, or embossing the precursor
ceramic abrasive particle into a predetermined shape or pattern. Non-limiting examples
of formed ceramic abrasive particles include shaped abrasive particles, such as triangular
plates as disclosed in
U.S. patents RE 35,570;
5,201,916;
5,984,998;
8,034,137;
8,123,828;
8,142,531;
8,142,532; and
8,142,891; and in
U.S. patent publications 2009/0169816,
2010/0146867, and
2010/0319269 or elongated ceramic rods/filaments often having a circular cross section produced
by Saint-Gobain Abrasives an example of which is disclosed in
U.S. patent number 5,372,620. Formed ceramic abrasive particles are generally homogenous or substantially uniform
and maintain their sintered shape without the use of a binder such an organic or inorganic
binder that bond smaller abrasive particles into an agglomerated structure and excludes
abrasive particles obtained by a crushing or comminution process that produces abrasive
particles of random size and shape. In many embodiments, the formed ceramic abrasive
particles comprise a homogeneous structure of sintered alpha alumina or consist essentially
of sintered alpha alumina.
[0052] The formed ceramic abrasive particles can be graded to a nominal screened grade using
U.S.A. Standard Test Sieves conforming to ASTM E-11 "Standard Specification for Wire
Cloth and Sieves for Testing Purposes." ASTM E-11 proscribes the requirements for
the design and construction of testing sieves using a medium of woven wire cloth mounted
in a frame for the classification of materials according to a designated particle
size. A typical designation may be represented as -18+20 meaning that the formed ceramic
abrasive particles pass through a test sieve meeting ASTM E-11 specifications for
the number 18 sieve and are retained on a test sieve meeting ASTM E-11 specifications
for the number 20 sieve. In one embodiment, the formed ceramic abrasive particles
have a particle size such that most of the formed ceramic abrasive particles pass
through an 18 mesh test sieve and can be retained on a 20, 25, 30, 35, 40, 45, or
50 mesh test sieve. In various embodiments of the invention, the formed ceramic abrasive
particles can have a nominal screened grade comprising: -18+20 (925 µm), -20+25 (780
µm), -25+30 (655 µm), -30+35 (550 µm), -35+40 (463 µm), -40+45 (390 µm), -45+50 (328
µm), -50+60 ( 275 µm), -60+70 (231 µm), -70+80 (196 µm), -80+100 (165 µm), -100+120
(138 µm), -120+140 (116 µm), -140+170 (98 µm), -170+200 (83 µm), -200+230 (69 µm),
- 230+270 (58 µm), -270+325 (49 µm), -325+400 (42 µm), -400+450 (35 µm), -450+500
(29 µm), or -500+635 (23 µm).
[0053] The average particle size is the expected average size of abrasive particles conforming
to the industry specified grade or in the case of sieves, the average between the
size of the screen opening the particle passed through and the size of the screen
opening the particle was retained on. The number in parenthesis following the grade
or screen designation is the average abrasive particle size in µm.
Filler particles
[0054] Filler particles may be blended with abrasive particles in the abrasive article.
Examples of useful fillers include metal carbonates (such as calcium carbonate, calcium
magnesium carbonate, sodium carbonate, magnesium carbonate), silica (such as quartz,
glass beads, glass bubbles and glass fibers), silicates (such as talc, clays, montmorillonite,
feldspar, mica, calcium silicate, calcium metasilicate, sodium aluminosilicate, sodium
silicate), metal sulfates (such as calcium sulfate, barium sulfate, sodium sulfate,
aluminum sodium sulfate, aluminum sulfate), gypsum, vermiculite, sugar, wood flour,
aluminum trihydrate, carbon black, metal oxides (such as calcium oxide, aluminum oxide,
tin oxide, titanium dioxide), metal sulfites (such as calcium sulfite), thermoplastic
particles (such as polycarbonate, polyetherimide, polyester, polyethylene, poly(vinylchloride),
polysulfone, polystyrene, acrylonitrile-butadiene-styrene block copolymer, polypropylene,
acetal polymers, polyurethanes, nylon particles) and thermosetting particles (such
as phenolic bubbles, phenolic beads, polyurethane foam particles and the like). The
filler may also be a salt such as a halide salt. Examples of halide salts include
sodium chloride, potassium cryolite, sodium cryolite, ammonium cryolite, potassium
tetrafluoroborate, sodium tetrafluoroborate, silicon fluorides, potassium chloride,
magnesium chloride. Examples of metal fillers include, tin, lead, bismuth, cobalt,
antimony, cadmium, iron and titanium. Other miscellaneous fillers include sulfur,
organic sulfur compounds, graphite, lithium stearate and metallic sulfides.
[0055] In some embodiments, the abrasive particles are treated with a coupling agent (e.g.,
an organosilane coupling agent) to enhance adhesion of the abrasive particles to the
binder. The abrasive particles may be treated before combining them with the binder
material, or they may be surface treated in situ by including a coupling agent to
the binder material.
Grinding Aids
[0056] In some embodiments, bonded abrasive wheels according to the present disclosure contain
additional grinding aids such as, for example, polytetrafluoroethylene particles,
cryolite, sodium chloride, FeS2 (iron disulfide), or KBF4; typically in amounts of
from 1 to 25 percent by weight, more typically 10 to 20 percent by weight, subject
to weight range requirements of the other constituents being met. Grinding aids are
added to improve the cutting characteristics of the cut-off wheel, generally by reducing
the temperature of the cutting interface. The grinding aid may be in the form of single
particles or an agglomerate of grinding aid particles. Examples of precisely shaped
grinding aid particles are taught in U.S. Patent Publ. No.
2002/0026752 A1 (Culler et al).
Backings
[0057] Useful backings include, for example, paper, fabric, scrim or open weave backings,
or film backings. Suitable film backings include polymeric films and primed polymeric
films, especially those used in the abrasive arts. Useful polymeric films include,
for example, polyester films (e.g., an ethylene-acrylic acid copolymer primed polyethylene
terephthalate), polyolefin films (e.g., polyethylene or polypropylene films), and
elastic polyurethane films. The film backing may be a laminate of two polymeric films.
Examples of elastomeric polyurethanes that may be used to form films include those
available under the trade designation ESTANE from B.F. Goodrich and Co. of Cleveland,
OH and those described in
U.S. Pat. Nos. 2,871,218 (Schollenberger);
3,645,835 (Hodgson);
4,595,001 (Potter et al.);
5,088,483 (Heinecke);
6,838,589 (Liedtke et al.); and
RE 33,353 (Heinecke). Pressure-sensitive adhesive-coated polyurethane elastomer films are commercially
available from 3M Company under the trade designation TEGADERM Useful polymeric films
are generally from about 0.02 to about 0.5 millimeters in thickness, for example,
from 0.02 millimeter to 0.1 millimeter in thickness; however, this is not a requirement.
Binder
[0058] The binder material typically comprises a glassy inorganic material (e.g., as in
the case of vitrified abrasive wheels), metal, or an organic resin (e.g., as in the
case of resin-bonded abrasive wheels).
[0059] Glassy inorganic binders may be made from a mixture of different metal oxides. Examples
of these metal oxide vitreous binders include silica, alumina, calcia, iron oxide,
titania, magnesia, sodium oxide, potassium oxide, lithium oxide, manganese oxide,
boron oxide, phosphorous oxide, and the like. Specific examples of vitreous binders
based upon weight include, for example, 47.61 percent S1O2, 16.65 percent AI2O3, 0.38
percent Fe2 O3, 0.35 percent T1O2, 1.58 percent CaO, 0.10 percent MgO, 9,63 percent
Na20, 2.86 percent]¾0, 1.77 percent L12O, 19.03 percent B2O3, 0.02 percent Mn02, and
0.22 percent P2O5 ; and 63 percent S1O2, 12 percent AI2O3, 1.2 percent CaO, 6.3 percent
Na20, 7.5 percent]¾0, and 10 percent B2O3. During manufacture of a vitreous bonded
abrasive wheel, the vitreous binder, in a powder form, may be mixed with a temporary
binder, typically an organic binder. The vitrified binders may also be formed from
a frit, for example anywhere from about one to 100 percent frit, but generally 20
to 100 percent frit. Some examples of common materials used in frit binders include
feldspar, borax, quartz, soda ash, zinc oxide, whiting, antimony trioxide, titanium
dioxide, sodium silicofluoride, flint, cryolite, boric acid, and combinations thereof.
These materials are usually mixed together as powders, fired to fuse the mixture and
then the fused mixture is cooled. The cooled mixture is crushed and screened to a
very fine powder to then be used as a frit binder. The temperature at which these
frit bonds are matured is dependent upon its chemistry, but may range from anywhere
from about 600° C to about 1800° C.
[0060] Examples of metal binders include tin, copper, aluminum, nickel, and combinations
thereof.
[0061] Organic binder materials are typically included in an amount of from 5 to 30 percent,
more typically 10 to 25, and more typically 15 to 24 percent by weight, based on the
total weight of the bonded abrasive wheel. Phenolic resin is the most commonly used
organic binder material, and may be used in both the powder form and liquid state.
Although phenolic resins are widely used, it is within the scope of this disclosure
to use other organic binder materials including, for example, epoxy resins, urea-
formaldehyde resins, rubbers, shellacs, and acrylic binders. The organic binder material
may also be modified with other binder materials to improve or alter the properties
of the binder material. Useful phenolic resins include novolac and resole phenolic
resins. Novolac phenolic resins are characterized by being acid-catalyzed and having
a ratio of formaldehyde to phenol of less than one, typically between 0.5: 1 and 0.8:1.
Resole phenolic resins are characterized by being alkaline catalyzed and having a
ratio of formaldehyde to phenol of greater than or equal to one, typically from 1
: 1 to 3 : 1. Novolac and resole phenolic resins may be chemically modified (e.g.,
by reaction with epoxy compounds), or they may be unmodified. Exemplary acidic catalysts
suitable for curing phenolic resins include sulfuric, hydrochloric, phosphoric, oxalic,
and p-toluenesulfonic acids. Alkaline catalysts suitable for curing phenolic resins
include sodium hydroxide, barium hydroxide, potassium hydroxide, calcium hydroxide,
organic amines, or sodium carbonate.
[0062] Phenolic resins are well-known and readily available from commercial sources. Examples
of commercially available novolac resins include DUREZ 1364, a two-step, powdered
phenolic resin (marketed by Durez Corporation of Addison, Texas under the trade designation
VARCUM (e.g., 29302), or HEXION AD5534 RESIN (marketed by Hexion Specialty Chemicals,
Inc. of Louisville, Kentucky). Examples of commercially available resole phenolic
resins useful in practice of the present disclosure include those marketed by Durez
Corporation under the trade designation VARCUM (e.g., 29217, 29306, 29318, 29338,
29353); those marketed by Ashland Chemical Co. of Bartow, Florida under the trade
designation AEROFENE (e.g., AEROFENE 295); and those marketed by Kangnam Chemical
Company Ltd. of Seoul, South Korea under the trade designation "PHENOLITE" (e.g.,
PHENOLITE TD-2207).
[0063] Curing temperatures of organic binder material precursors will vary with the material
chosen and wheel design. Selection of suitable conditions is within the capability
of one of ordinary skill in the art. Exemplary conditions for a phenolic binder may
include an applied pressure of about 20 tons per 4 inches diameter (224 kg/cm^) at
room temperature followed by heating at temperatures up to about 185°C for sufficient
time to cure the organic binder material precursor.
[0064] Bonded abrasive articles according to various embodiments may take any of a variety
of conventional forms. Preferred abrasive articles are in the form of wheels. Abrasive
wheels are typically in the form of a disc or right cylinder having dimensions that
may be very small, e.g., a cylinder height on the order of a few millimeters or very
large, e.g., a meter or more, and a diameter which may be very small, e.g., on the
order of a few centimeters, or very large, e.g., tens of centimeters. Wheels typically
have a central opening for support by an appropriate arbor or other mechanical holding
means to enable the wheels to be rotated during use. Wheel dimensions, configurations,
means of support, and means of rotation are all well known in the art.
[0065] The abrasive particles may, for example, be uniformly or non-uniformly distributed
throughout the bonded abrasive article. For example, if the bonded abrasive article
is a grinding wheel or a cut-off wheel, the abrasive particles may be concentrated
toward the middle (e.g., located away from the outer faces of a grinding or cut-off
wheel), or only in the outer edge, i.e., the periphery, of a grinding or cut-off wheel.
The depressed-center portion may contain a lesser amount of abrasive particles. In
another variation, first abrasive particles may be in one side of the wheel with different
abrasive particles on the opposite side. However, typically all the abrasive particles
are homogenously distributed among each other, because the manufacture of the wheels
is easier, and the cutting effect is optimized when the two types of abrasive particles
are closely positioned to each other.
[0066] Optionally, bonded abrasive articles according to various embodiments may further
comprise a scrim that reinforces the bonded abrasive article; for example, disposed
on one or two major surfaces of the bonded abrasive article, or disposed within the
bonded abrasive article. Examples of scrims include a woven or a knitted cloth. The
fibers in the scrim may be made from glass fibers (e.g., fiberglass), organic fibers
such as polyamide, polyester, or polyimide. In some instances, it may be desirable
to include reinforcing staple fibers within the bonding medium, so that the fibers
are homogeneously dispersed throughout the bonded abrasive article.
EXAMPLES
[0067] Objects and advantages of this disclosure are further illustrated by the following
non-limiting examples. The particular materials and amounts thereof recited in these
examples as well as other conditions and details, should not be construed to unduly
limit this disclosure. Unless otherwise noted, all parts, percentages, ratios, etc.
in the Examples and the rest of the specification are by weight.
Materials
[0068]
| ABBREVIATION |
DESCRIPTION |
| AP1 |
alumina abrasive particle, TREIBACHER 36 BFRPL, obtained from Treibacher Schleifmettel,
AG, Villach, Austria |
| AP2 |
ceramic alumina abrasive particle, 3M™ CERAMIC ABRASIVE GRAIN 321, GRADE 36, from
3M, Saint Paul, Minnesota |
| PR1 |
liquid phenolic resin, DUREZ 8121, obtained from Sumitomo Bakelite North America,
Manchester Connecticut |
| PR2 |
powder phenolic resin, VARCUM 29302, obtained from Sumitomo Bakelite North America |
| CRY1 |
sodium hexafluoroaluminate (cryolite), obtained from FREEBEE A/S, Farum, Denmark |
| PR3 |
resole phenolic resin, 70% solids condensate of a 1.96:1 formaldehyde:phenol mixture
with 2% potassium hydroxide catalyst (on weight of phenol) in water |
| SCRIM |
fiberglass mesh, obtained as STYLE 4400 from Industrial Polymers and Chemicals, Inc.,
Shrewsbury, Massachusetts |
| SAP1 |
Grade 36+ shaped abrasive particles prepared according to the disclosure of U.S. Pat. No. 8,142,531 having a side length of about 0.8mm and about 0.2 mm thick, and a sidewall angle
of 98 degrees. |
| AP3 |
abrasive particles, available as ESK, RBT9 BROWN CORUNDUM # 30 from Treibacher Schleifmettel
AG |
| AP4 |
abrasive particles, available as FRSK SEMI-FRIABLE CORUNDUM #36 from Treibacher Schleifmettel
AG |
| AP5 |
abrasive particles, available as WHITE ALUMINUM OXIDE FEPA grade 800 from Stanchem
Sp. Zo.o., Lublin, Poland |
| PR1 |
liquid phenolic resin, available as PA 5614G from PA Resins AB, Stockholm, Sweden |
| PR2 |
phenolic resin powder available as DYNEA 8551G from Dynea Oy Corp. |
| PR4 |
phenolic resin powder available as DYNEA 8126G from Dynea Oy Corp. |
| CRY2 |
Sodium hexafluoroaluminate, obtained as Cryolite from Solvay Fluor GmbH, Hannover,
Germany |
| CACO |
calcium carbonate, obtained as HUBERCARB Q4 from Huber Engineered Materials, Quincy
Illinois |
| CRY3 |
potassium fluoroaluminate, particle size distribution d10 = 2.58 micrometers, d50=11.5 micrometers, d90=36.6 micrometers, from KBM Afflips B.V., Oss, The Netherlands. |
| CB |
carbon black pigment, available as CORAX N339 from Carbon Black Polska Sp. Z o.o.,
Jaslo, Poland |
| silane |
adhesion promoter, DYANSYLAN from Evonik Industries AG, Hanau-Wolfgang, Germany. |
| solvent |
furfuryl alcohol |
| oil |
paraffin oil |
| water |
tap water |
| SURF |
ethoxylated oleic acid surfactant, obtained as EMULAN A from BASF, Ludwigshafen, Germany |
Abrasive Article Preparation
Examples 1 - 8
[0069] Abrasive articles of Example 1 through Example 8 were prepared using conventional
and shaped abrasive particles of various sizes.
Example 1
[0070] An abrasive article was prepared in the form of a depressed-center grinding wheel
(a type-27 grinding wheel) as follows.
Mix 1 was formed by mixing 860 grams of AP1 and 55 grams of PR1 using an air mixer.
Mix 2 was prepared by mixing 155 grams PR2, 155 grams CRY1 for 1 minute in a paddle
type mixer.
Mix 3 was prepared by mixing Mix 1 and Mix 2 in a paddle type mixer for 10 minutes.
Mix 4 was prepared by mixing 860 grams SAP1 and 55 grams of PR1 with a high shear
air mixer.
Mix 5 was prepared by combining Mix 2 and Mix 4 and mixing in a paddle type mixer
for 10 minutes.
Mix 6 was prepared by combining 700g of Mix 3 and 300g of Mix 5 and mixing in a paddle
type mixer for 10 minutes.
[0071] A 6.75 in. (17.1 cm) diameter disc of SCRIM was placed in a 7" (18 cm) cavity die.
250 grams of Mix 6 was spread out evenly on the scrim and a second 6.75 in. SCRIM
was placed on top of the mixture. The filled cavity mold was then pressed at 40 ton/38
sq. inch (14.51 MPa) to form a disc.
[0072] Multiple resulting discs were then placed on a spindle between depressed center aluminum
plates in order to be pressed into type 27 depressed-center grinding wheels. The discs
were compressed at 5 ton/38 sq. inch (1.81 MPa). The compressed discs were cured in
an oven by heating for 7 hours at 79° C, 3 hours at 107° C, 18 hours at 185° C, and
followed by a ramp down over 4 hours to 27° C to form cured discs. The cured discs
had a diameter of 180mm and a thickness of 4 mm, with a central hole of diameter 7/8"
(2,22 cm)
[0073] The cured discs were spray coated with 15 grams of a make resin mix consisting of
51 parts PR3, 42 parts CACO, 6 parts water, and 1 part SURF to be ready for electrostatic
mineral coat. A layer of about 47 grams of SAP1 was deposited on top of the sample.
Then the discs were cured at 226° F (108 °C) for 90 minutes.
[0074] The mineral coated discs were then sized by spraying the size resin mix consisting
of 45 parts PR3, 53 parts CRY2, and 2 parts CB, followed by curing at 190° F (88 °C)
for 80 minutes. Finally, the dried discs were cured for 12 hours at 212° F (100 °C)
to form grinding wheels.
[0075] The grinding wheels were tested by grinding by hand for ten 1- minute cycles on a
mild steel bar 0.5" (1,27 cm) thick and 18" (45,72 cm) long using a 6000 RPM air grinder
(Ingersoll-Rand) The grinder weight resulted in an applied load of 13 lbs. (5.9 kg)
The weight of the steel bar was measured before and after each cycle to measure the
cut. The grinding was repeated 16 times from end to end per cycle, approximately 1
minute each. The weight lost from the grinding disc was recorded after each test.
The grinding test results are summarized in Table 1.
Example 2
[0076] Grinding wheels were prepared as in Example I, with additional spray coating with
15 grams of the make resin mix of Example 1, in preparation for electrostatic mineral
coat after the first curing. A second layer of SAP1 was deposited on top of the first
layer of SAP1, weighing about 47 g. Then the sample was cured at 226° F (108 C) for
90 minutes.
[0077] The mineral coated discs were then sized by spraying the size resin mix of Example
1, followed by curing at 190° F (88 C) for 80 minutes.
[0078] Finally, the dried discs were cured for 12 hours at 212° F(100 C) to form grinding
wheels. The grinding test results are summarized in Table 1.
Example 3
[0079] Grinding wheels were prepared as in Example 1, substituting the electrostatic mineral
coated SAP1 with AP2. The grinding test results are summarized in Table 1.
Example 4
[0080] Grinding wheels were prepared as in Example 1, but Mix 6 was substituted by Mix 7
(40 parts Mix3 and 60 parts Mix4). The grinding test results are summarized in Table
1.
Example 5
[0081] Grinding wheels were prepared as in Example 4, substituting the electrostatic mineral
coated precision shaped grain mineral layer with AP2. The grinding test results are
summarized in Table 1.
Example 6
[0082] A depressed-center grinding wheel was prepared according to the following procedure.
[0083] Mix 8 was prepared by mixing 430 grams of SAP1, 430 grams of AP1, 72 grams of PR1,
and 2 grams of CB for 1 minute using a high shear air mixer
[0084] Mix 9 was prepared by mixing 175 grams of PR2 and 151 grams CRY1 for 1 minute in
a paddle type mixer.
[0085] Mix 10 was prepared by combining Mix 8 and Mix 9 and mixing in a paddle type mixer
for 10 minutes.
[0086] Mix 10 was then screened through a screen with 2x2 mm openings to remove agglomerates.
This screened mixture was then pressed in 178 mm diameter dies. SCRIM was placed in
the die, 200 grams of Mix 10 was spread out evenly and a second fiberglass mesh was
placed on top of the mix. A metal center hole bushing was added. This mix was then
pressed at 40 ton/ 38 sq. inch (14.5 MPa) to form discs.
[0087] These discs were placed on a spindle between depressed center aluminum plates in
order to be pressed to form type 27 depressed-center grinding wheels. A stack of 5
plates and pressed discs were compressed at 5 ton/38 sq.inch (1.8 MPa). The discs
were cured in an oven for 7 hours at 79° C, 3 hours at 107° C, 18 hours at 185° C,
and ramp down over 4 hours to 27° C. The cured discs had a diameter of 180mm and a
thickness of 4 mm, with a central hole of diameter 22,32 mm.
[0088] The working surface of the disc was coated SAP1 by the following procedure. The discs
were spray coated with 15 gm of the make resin mix of Example 1. A layer of SAP1 weighing
about 42 grams was deposited on top of the disc. Then the disc was cured at 226° F
(108 C) for 75 minutes. Next, in order to have the sized sample, the mineral coated
disc was sprayed with the size resin mix of Example 1. Then, it was cured at 190°
F (88 C) for 80 minutes.
[0089] Finally, the dried discs were cured for 12 hours at 212° F (100 C) to produce grinding
wheels for testing.
[0090] The grinding wheels were tested by grinding by hand for ten 1- minute cycles on a
mild steel bar 0.5" (1,27 cm) thick and 18" (45,72 cm) long using a 6000 RPM air grinder
(Ingersoll-Rand) The grinder weight resulted in an applied pressure of 13 lbs (5,9
kg). The weight of the steel bar was measured before and after each cycle to measure
the cut. The grinding was repeated 16 times from end to end per cycle, approximately
1 minute each. The weight lost from the grinding disc was recorded after each test.
The grinding test results are summarized in Table 2.
Example 7
[0091] Commercially available depressed center grinding wheels (92309, 7"x1/8"x7/8", (17,8
cm x 0,3 cm x 2,2 cm) 3M Company, Thailand) were coated using the method of Example
6. The grinding test results are summarized in Table 2.
Example 8
[0092] 7" x 1/8" x 7/8" (17,8 cm x 0,3 cm x 2,2 cm) discs were prepared by mixing 23 parts
AP3, 38 parts SAP1, 15 parts AP4, 4 parts PR1, 6 parts PR2, 4 parts PR4, 3 parts CRY3,
2 parts AP5, 4 parts CRY2, 0.1 part CB, 0.2 parts silane, 0.3 parts solvent, and 0.4
parts oil. The components were mixed for 10 minutes. The prepared discs were compressed,
coated and cured into grinding wheels as in Example 6. The grinding test results are
summarized in Table 2.
Comparative Example 1
[0093] Grinding wheels were prepared as Example 1, without the grinding layer. The grinding
test results are summarized in Table 1.
Comparative Example 2
[0094] Grinding wheels were prepared as in Example 4, without the grinding layer. The grinding
test results are summarized in Table 1.
Comparative Example 3
[0095] 7"x1/8"x7/8" (17,8 cm x 0,3 cm x 2,2 cm) depressed center grinding wheels were prepared
as in Example 6, without the additional coated abrasive layer. The grinding test results
are summarized in Table 2.
Comparative Example 4
[0096] Commercially available depressed center grinding wheels (92309, 7"x1/8"x7/8", (17,8
cm x 0,3 cm x 2,2 cm) 3M Company, Thailand) without the added grinding layer of Example
6. The grinding test results are summarized in Table 2.
Comparative Example 5
[0097] 7"x1/8"x7/8" (17,8 cm x 0,3 cm x 2,2 cm) depressed center grinding wheels were prepared
as in Example 8, but without the coated abrasive layer. The grinding test results
are summarized in Table 2.
Table 1
| |
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Comparative Example 1 |
Comparative Example 2 |
| Disc Wear (grams) |
14.3 |
19.6 |
18.6 |
12.5 |
18.3 |
10.1 |
10.3 |
| Cut cycle 1 |
43.2 |
48.7 |
37.6 |
53 |
33.2 |
39.9 |
53.3 |
| Cut cycle 2 |
35 |
42.3 |
42.2 |
48.2 |
31.9 |
29.1 |
37.9 |
| Cut cycle 3 |
36.3 |
45 |
32.5 |
49.2 |
34.2 |
27.6 |
30.4 |
| Cut cycle 4 |
32 |
42.2 |
27 |
48.2 |
37.1 |
24.7 |
27 |
| Cut cycle 5 |
28 |
43.5 |
28.2 |
40.1 |
30.8 |
21.6 |
28.3 |
| Cut cycle 6 |
28.4 |
43.5 |
30.6 |
36.3 |
33.4 |
25.3 |
25.1 |
| Cut cycle 7 |
28.8 |
37.8 |
28.3 |
38.7 |
30.5 |
23.7 |
26.2 |
| Cut cycle 8 |
26.3 |
39.1 |
28.9 |
36 |
27 |
23.2 |
28.6 |
| Cut cycle 9 |
26.3 |
31.9 |
25.9 |
35.2 |
33.7 |
26.5 |
28.9 |
| Cut cycle 10 |
28.7 |
31.5 |
25.1 |
33.4 |
33.3 |
24.7 |
30.2 |
| Total Cut (gms) |
313 |
405.5 |
306.3 |
418.3 |
325.1 |
266.3 |
315.9 |
| G Ratio |
22 |
21 |
16 |
33 |
18 |
26 |
30 |
Table 2
| |
Example 6 |
Example 7 |
Example 8 |
Comparative Example 3 |
Comparative Example 4 |
Comparative Example 5 |
| Disc Wear, grams |
14.14 |
15 |
16.1 |
8.57 |
9 |
7.1 |
| Cut cycle 1 |
57.7 |
70.4 |
74.6 |
36.6 |
32 |
26.6 |
| Cut cycle 2 |
56.3 |
57.2 |
66.5 |
27 |
21.5 |
25.8 |
| Cut cycle 3 |
48 |
50 |
51.9 |
35.1 |
19.6 |
21.8 |
| Cut cycle 4 |
45.2 |
42.2 |
38.1 |
30 |
13.3 |
16 |
| Cut cycle 5 |
41.2 |
32.1 |
37.9 |
28.1 |
18.1 |
13.2 |
| Cut cycle 6 |
42.7 |
26.1 |
46.6 |
29.6 |
15.1 |
24.7 |
| Cut cycle 7 |
42 |
27.1 |
34.2 |
28.5 |
15.4 |
29 |
| Cut cycle 8 |
36.3 |
29.8 |
28.5 |
26.4 |
12.9 |
19.1 |
| Cut cycle 9 |
36.4 |
21.3 |
32 |
25.4 |
15.1 |
17.3 |
| Cut cycle 10 |
33.2 |
25.5 |
28.9 |
22.1 |
18.8 |
15.4 |
| Total Cut, grams |
439 |
382 |
439 |
289 |
182 |
209 |
| G Ratio |
31 |
25 |
27 |
34 |
20 |
29 |
| Comparison of Examples |
% Total Cut Improvement |
| Example 1 compared to Comparative Example 1 |
18 % |
| Example 2 compared to Comparative Example 1 |
52 % |
| Example 3 compared to Comparative Example 1 |
15 % |
| Example 4 compared to Comparative Example 2 |
32 % |
| Example 5 compared to Comparative Example 2 |
3 % |
Discussion of Test Results
[0098] Table 3 presents a comparative analysis of the grinding performance of grinding wheels
according to Examples 1 through 5 and Comparative Examples 1 through 2.
Table 3
| Comparison of Examples |
% Total Cut Improvement |
| Example 1 compared to Comparative Example 1 |
18 % |
| Example 2 compared to Comparative Example 1 |
52 % |
| Example 3 compared to Comparative Example 1 |
15 % |
| Example 4 compared to Comparative Example 2 |
32 % |
| Example 5 compared to Comparative Example 2 |
3 % |
[0099] As can be seen in Table 3, grinding wheels according to various embodiments exhibit
significantly improved total cut and grinding performance.
[0100] Other modifications and variations to the present disclosure may be practiced by
those of ordinary skill in the art, without departing from the scope of the present
disclosure, which is more particularly set forth in the appended claims. The preceding
description, given in order to enable one of ordinary skill in the art to practice
the claimed disclosure, is not to be construed as limiting the scope of the disclosure,
which is defined by the appended claims.