CA2227518A1 - Method for making a spliceless coated abrasive belt - Google Patents

Method for making a spliceless coated abrasive belt Download PDF

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Publication number
CA2227518A1
CA2227518A1 CA002227518A CA2227518A CA2227518A1 CA 2227518 A1 CA2227518 A1 CA 2227518A1 CA 002227518 A CA002227518 A CA 002227518A CA 2227518 A CA2227518 A CA 2227518A CA 2227518 A1 CA2227518 A1 CA 2227518A1
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CA
Canada
Prior art keywords
backing
front surface
spliceless
coating
abrasive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002227518A
Other languages
French (fr)
Inventor
Todd J. Christianson
Harold W. Benedict
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Co
Original Assignee
Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2227518A1 publication Critical patent/CA2227518A1/en
Abandoned legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical 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
    • B24D3/20Physical 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
    • B24D3/28Resins or natural or synthetic macromolecular compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • B24D11/02Backings, e.g. foils, webs, mesh fabrics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • B24D11/06Connecting the ends of materials, e.g. for making abrasive belts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D18/00Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for
    • B24D18/0036Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for by winding up abrasive bands

Abstract

A method of making a flexible coated abrasive belt comprising the steps of: mounting an endless, spliceless backing loop substrate having an exposed front surface and a back surface tautly on a peripheral surface of a temporary support structure; applying a continuous fibrous reinforcing material onto said front surface in a plurality of revolutions; applying a coating of a first binder precursor onto said front surface; exposing said coating to conditions effective to solidify said first binder precursor and bond said fibrous reinforcing material to said front surface to form an endless spliceless reinforced backing; and applying an abrasive coating comprising abrasive particles and adhesive over said back surface or said front surface of said endless spliceless reinforced backing.

Description

CA 02227~18 1998-01-21 w o 97/05990 PCTAUS96/12791 M E T H O D F O R M A KIN G- A ~P LIC E L ESS C O AlrE D ~IBI~SI~E B E L T

Baclkground of the Inventio l. Field of the Invention The present invention yertains to a method for making a spliceless coated 10 abrasive belt reinforced by a continuous elongate fibrous material, and the product of this method.
2. Re1ated Art Coated abrasive articles generally contain an abrasive material, typically in 15 the form of abrasive grains, bonded to a backing by means of one or more adhesive layers. Such articles usually take the form of substrates, discs, belts, bands, and the like, which can be adapted to be mounted on pulleys, wheels, or drums. Abrasive articles can be used for sanding, grinding, or polishing various surfaces of, for example, steel and other metals, wood, wood-like l~min~te~s, plastic, fiberglass, 2 0 leather, or ceramics.
The backings used in coated abrasive articles are typically made of paper, polymeric m~teri~l.c, cloth, nonwoven m~teri~l~, vulcanized fiber, or combinations of these materials. Many of these m~t.o.ri~l~ alone provide lln~cceptable b~ ingc for certain applications because they are not of sufficient strength, flexibility, or 2 5 impact resistance. As a result, early failure and poor functioning can occur, at least in certain applications of these backing materials in a nonreinforced state.
In a typical m~n11f~ft 1ring process, a coated abrasive article, including the b~ ing and abrasive coating, almong other things, is made in a continuous web form and thereafter converted into a desired construction, such as a substrate, disc, 3 0 belt, or the like. One of the most useful constructions of a coated abrasive article is an endless coated abrasive belt, i.e., a continuous loop of coated abrasive material.
In order to form such an endless belt, the web form is typically cut into an elongate CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 strip of a desired width and length. The ends of the elongate strip of the plcro~ ed substrate of coated abrasive article are then joined together to create a "joint" or a "splice".
There are two commons ways to join the free ends of an elongate strip to make a spliced endless belt. These are respectively referred to as a "lap" splice or a "butt" splice. In a "lap" splice, the two free ends of the elongate strip are respectively beveled to have a top end and a bottom end which can be superposed to form a joint without causing a significant change in the overall thickness of the belt. The beveling on what will become the bottom end is typically accomplished by removing abrasive grains and m~teri~l from the abrasive surface of one end ofthe strip and removing part of the material from the backing or underside of theother end of the strip to provide what will become the top end of the splice. The beveled ends are then overlapped and joined adhesively or mechanically.
For the "butt" splice, the two free mating ends of the elongate strip are brought into a juxtaposed relationship at a juncture line. The bottom surface of the backing at each end of the elongate strip, such as a preformed substrate of coated abrasive article, typically is then coated with an adhesive, me(~h~nic~lly secured, or otherwise attached, and maybe overlaid with a strong, thin, tear-recict~nt, splicing media in the joint area.
2 0 Lap and butt splices, while providing a satisfactory belt for many applications, may be undesirable for other applications because they typically create a disco~l~inuily in the abrasive coating layer at the outer surface, i.e., the abrasive coating surface, of the splice site. This type of splice is generally exemplified in U.S. Patent Nos. 2,391,731 (Miller), 3,333,372 (Gianatsio) and 2 5 4,736,549 (Toillie). A discontinuity in a coated abrasive can cause an undesirable mark in the surface of a workpiece being finished. These marks are often referred to as "chatter".
Other background art includes:
U.S. Patent No. 289,879 (Almond) pertains to a polishing tool comprising 3 0 abrasive grains adhered to a tubular backing.

CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 U.S. Patent No. 2,012,356 (Ellis) discloses a coated abrasive having a seamless tubular fabric backing.
U.S. Patent No, 2,404,207 (Ball) pertains to a seamless coated abrasive article having a fibrous 5 nonwoven backing. The fibrous nonwoven backing can be saturated with an adhesive and contain other reinforcing fibers.
U.S. Patent No. 2,41 1,724 (Hill) teaches a method for making an endless tubular coated abrasive, wherein a thermoplastic or thermosetting adhesive is extruded to form a b~ckin~, in which abrasive grains are embedded while the 10 backing is molten. In another embodiment of that invention, the b~rkin~ can comprise a liner of reinforcing strands over which is coated the thermoplastic adhesive.
French Patent Application lPublication No. 2,396,625 published 2 February 1979 teaches a seamless endless coated abrasive belt that is made by the 15 continuous weaving of a cloth b~çking This reference also describes a spliced backing having a sinusoidal splice.
French Patent Publication 2,095,185 published 2 November 1972 (Ponthelet) discloses an abrasive product having a nonwoven backing which may be reinforced with filaments placed in either the transversal direction, longit~ in~l 2 0 direction or as a grid form. Where the filaments are arranged only in one direction, the fil~mPnt~ are said to be m~;nt~ined in a parallel arrangement as held down by a veil made of natural, artificial or synthetic fibers.
PCT Published Patent Application No. WO 93/12911 (Benedict et al.) published 8 July 1993 and owned by the present ~cignt?e, pertains to a method of2 5 making a spliceless coated abrasive belt having a backing which includes between about 40 to 99% by weight of an organic polymeric binder and an effective amountof a fibrous reinforcing m~t~ri~l engulfed within the organic polymeric binder material. This reference described ~lcp~;llg a loop of liquid binder material having fibrous reinforcing m:~teri5ll therein around the periphery of a drum~ and 3 0 then solidifying the binder m~t~n~l to forrn the endless, spliceless belt.

CA 02227~18 1998-01-21 In many abrading applications, it is desired to use an endless coated abrasive belt t-h-at has a bzleking with certain desired physical properties. These plopt;~lies include relatively low stretch, relatively high tensile skength value and relatively high adhesion between the backing and the abrasive coating. Although Benedict et al. l~r~;selll a significant advance in the art of making coated abrasive belts, alternate approaches to improve the physical properties of the backing continue to be sought.
PCT Published Patent Application No. WO 95/00294 published 5 January 1995 (Schneider et al.) and owned by the present assignee, pertains to a method of 1 0 making an endless, spliceless belt. A flowable organic material is spin casted to form an uncured endless loop of organic m~t~ri~k Abrasive particles are then inserted into the spin caster, spun therein until they are engulfed into the organic material which is then solidified to forrn an endless, spliceless abrasive belt.U.S. Patent 2,349,365 (Martin et al.) involves a flexible coated abrasive 1 5 article in which the backing comprises a substrate of plastic m~teri~l reinforced with a subskate of cloth or paper.
PCT Published Patent Application No. WO 86/02306 publication published 24 April 1986 (Hansen et al.) pertains to an improved coated abrasive b~ckinf~
having a flexible substrate and a multiplicity of weft free, closely spaced, sketch 2 0 rçci~t~nt, longitl-~lin~lly aligned, coplanar, continuous filarnent reinforcing yarns bonded to one surface of the flexible substrate before the backing is seamed into an endless belt. Each fil~ment of the plurality of yarns would have ends which mustbe joined to provide the backing subskate, providing a discolllhluily and probable weak area in the b~ king U.S. Application USSN 08/199,835 (Chri~ti~n~on et al.) filed 22 February 1994 and assigned to the present assignee, pertains to a endless, spliced abrasive b~king having reinforcing fibers.
PCT Published Patent Application No. WO 93/02837 (Luedeke et al.) published 18 February 1993 and assigned to the present assignee teaches the 3 0 dressing and truing of coated abrasive belts.

CA 02227~18 1998-01-21 W 097/05990 PCT~US96/12791 U.S. Application USSN 0~/199,679 (Benedict et al.) filed 22 February 1994 and assigned to the present assignee teaches a method of making an endless reinforced abrasive article comprising a sheet substrate, reinforcing fibrous mzlteri;ll, and a binder which bonds the fibrous m~t~ri~l to the substrate which also 5 doubles as a make coat for adhering abrasive grain to the substrate.
Users of spliceless coated abrasive belts continue to seek stronger, more durable coated abrasive belts which are substantially free of surface and/or thickness irregularities.

Sumnnaly of the Inventio~
The present invention pertains to a method for making a spliceless coated abrasive belt having a backing loop substrate reinforced by a continuous unspliced fibrous strand or strip materia], and the product of this method.
In one embodiment, the invention pertains to a method of making a flexible 15 coated abrasive belt comprising the steps of:
(a) mounting an ~nltlles~, spliceless backing loop substrate having an exposed front surface and a back surface tautly on a peripheral surface of a temporarv support structure;
(b) applying a continuous fibrous reinforcing material onto said front 2 0 surface in a plurality of revolutions;
(c) applying a coating of a first binder precursor onto the front surface;
(d) exposing said coating to conditions effective to solidify said first binder precursor and bond said fibrous reinforcing ~ .n~l to said front surface to form an endless spliceless reinforced b~king; and 2 5 (e) applying an abrasive coating comprising abrasive particles and adhesive over said back surface or said front surface of said endless splicelessreinforced backing.
The various steps shown in the method described above need not follow the sequence shown. It is to be understood that the application of the abrasive coating 3 0 to a surface of the backing substrate may precede the step of applying the fibrous CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 reinforcing material to the opposite surface of the backing substrate. Also, the step of applying the abrasive coating may be accomplished by applying a ~lefolll.ed abrasive coating which is formed in situ on either of the fiber reinforcing layer or the exposed surface backing substrate, or the abrasive coating may be applied by5 l~mins~ting a preform thereof on either one of such ~lrf~es It is also within the scope of this invention to apply the binder precursor to the fibrous reinforcing material before, simultaneous to, or after the applying of the fibrous reinforcing material to a surface of the spliceless loop of backing substrate.
It further is within the scope of the invention to use more than one binder 10 precursor to apply the fibrous reinforcing m~t-?ri~l to the b~c~ing substrate, such as by applying binder to the fibrous reinforcing m:~t~?ri~l and the surface of the backing substrate to be contacted with same.
It is further within the scope of this invention to apply several layers of fibrous reinforcing material to the spliceless backing substrate. These layers may 15 be formed of the same or dirr~lc;nt reinforcing m~teri~l~ Additionally, a single reinforcing layer may comprise several dirr~lell~ reinforcing m~t~ri~l~
For purposes of this invention, the term "endless, spliceless" in describing the b~ckinF subskate means that the backing substrate used in the belt has no free ends along its length direction, i.e., it is a closed loop. The endless spliceless 2 o backing loop substrate is preferably formed prior to in~ tion on the support structure.
For purposes of this invention, the fibrous reinforcing m~t~ri~l is applied to the spliceless backing loop substrate in a "continuous" manner in the sense that it is constituted by at least one individual fibrous skand or narrow fibrous strip wrapped 2 5 around the endless spliceless backing loop substrate more than one complete revolution of the fibrous .eillrolcillg material along the entire machine direction length of the loop.
The coated abrasive belts of the present invention are characterized by having one or more of the following improved properties. The endless spliceless 3 0 substrate loop provides a backing which is free of any high areas or splice marks.
The fiber reinforcement of the abrasive belt endows the abrasive belts of the CA 02227~18 1998-01-21 WO 97/O~99O PCT/US96/12791 invention with a greater resistance to stretch and an increased tensile strength and improved useful life. Obviously, the actual m~gnitu(le of improvement of these properties will depend in large part of the selection of the particular raw materials employed to make the abrasive belt, such a selection being within the capability of 5 ome skilled in the art who is aware of the present disclosure.
The method of the invention, in one embodiment, also provides a spliceless endless fiber reinforced backi;ng that then can be continuously coated with an abrasive coating along a surface thereof; thereby preventing the formation of discontinuities in the coated abrasive surface.
The fiber reinforcing layer of the invention can be subst~nti~lly completely surrounded by (i.e., engulfed within) the organic polymeric binder material. A
reinforcing layer is characterized by the presence of reinforcing fibers adjacent to t_e front surface of the substrate surface to which it is ~tt~rhecl and the absence of reinforcing fibers adjacent to its exposed surface. This provides a smooth, urliform exposed surface to the backing without any protruding fibrous reinforcing m~teri~l Furthermore, the surface topology is preferably prepared so that it is free of any waviness reflecting surface irregularities of fibrous reinforcing m~t~
Alttorn~tively, the reinforcing material can be wound with a wetting but not nPcec~rily engulfing amount of resin in an amount sufficient to immobilize the 2 0 fiber in place on the backing substrate after drying or curing.
In a more specific embodiment of the method of the invention, the applying of the lehlf~lcillg fiber onto the spiLiceless backing loop substrate provides aspacing of about 2-50 strands per cm of lateral width of the endless backing loop substrate.
2 5 An abrasive layer is applied to the surface of the fiber reinforced b~king loop described above to prepare an abrasive belt. The abrasive layer is typically applied to the back surface of the backing loop, i.e., the surface opposite the fiber reinforcement, but the abrasive layer may also be applied to the reinforced surface.
Conventional techniques are used to apply or create the abrasive layer.
3 o In a preferred embodiment of making the coated abrasive belt of the invention, abrasive particles are embedded in the second binder precursor layer CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 coated over the backing surface on which the abrasive layer will be applied. Such a coating is typically called a make coat. The abrasive particles are applied to the coating of second binder precursor by a coating technique selected from the group con~i~ting of electrostatic coating, drop coating, and magnetic coating.
The above method of making the abrasive coating further typically includes the step of applying a third binder precursor layer, as a so-called size coat, onto the embedded abrasive particles and then solidifying the binder precursor layers.
In one particular embodiment of the above-mentioned method, the manner of applying the fibrous reinforcing material comprises winding one individual fibrous reinforcing strand or narrow fibrous strip as a continuous element onto the spliceless backing loop substrate around the periphery of the front surface of the backing substrate in the form of a helix exten(ling longit~ in~lly to form the fiber reinforcing layer in a manner which covers substantially the entire lateral width of said front surface, and preferably covers the entire width thereof. The fibrous strand or narrow strip windings can be applied as a spiral winding side-by-side along the length of the surface of the backing substrate with their lateral edges in close ~ hllily to provide a substz-nti~lly continuous layer. This spiral winding of the reinforcing strand or strip on the preformed spliceless backing imparts increased strength and decreased stretchability to the backing.
2 0 The strand material can comprise any of a number of dirr~ types of nonmetallic or metallic fibrous m~teri~l, such as glass, steel, carbon, ceramic,wool, silk, cotton, cellulose, polyvinyl alcohol, polyamide, polyester, rayon, acrylic, polypropylene, aramid, and ultrahigh molecular weight polyethylenes.
In a pl~erel~,d embodiment of the method of the invention, the manner of 2 5 applying the fibrous reinforcing m~t~ri~l comprises separately winding each of at least a first individual reinforcing fibrous strand and a second individual reinforcing fibrous strand onto a spliceless backing loop substrate onto the front surface of the endless spliceless backing loop substrate in the form of a helix ext~n~ling longitudinally to form the fiber reinforcing layer that spans subst~nti~lly 3 0 the entire lateral width of the front surface of the endless backing substrate.
~lt~rn~t.-ly, the first and second individual reinforcing fibrous strands can be , CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 wound ~imlllt~nPously. The selection of diîr~elll types of wound fiber strands can be used to provide an improved balance of physical properties. For instance, in a combination of glass and polyarnide fiber strands, the glass strands impart low stretch p~Op~l ly while the polyamide strands offer strength to the fiber reinforcing 5 layer. As another example, a combination of aramid and polyester strands provides a balance of strength/low stretch and resilience7 respectively, in the fiber reinforcing layer. The reinforcing fiber m~t~ l also can be a narrow fibrous strip, such as a strip of woven or knitted fabric, nonwoven mat, or a tow, having a lateral width less than the lateral width of the backing ~ub~lldl~ to enable helical winding 10 thereon. Further, the reinforcing fiber can be applied in separate subsets across the lateral width of the spliceless lb~cking loop substrate. For example, continuous~hlfol~cillg fiber can be wound in multiple windings at lateral sides of the spliceless backing loop substrate and/or over a central area spaced from the side edges thereof.
In a further embodiment of the invention, the endless spliceless b~cl~ing loop substrate is particularly selected from the group con~i~ting of a polymeric film (including primed polymeric film)~ a woven cloth, a knitted cloth, paper, a vulcanized fiber substrate, a nonwoven, including combinations and treated versions thereof. For instance~ in a preferred embodiment, the endless spliceless 2 0 backing loop substrate can be xelected to be a cloth structure, such as a woven or knitted cloth.
In another further embodiment of the invention, the temporary support structure is a cylindrical surface. For example, a drum which is rotatable about its central axis by a motor drive and a drum which has an exp~ntl~ble and/or 2 5 collapsible periphery to permit adjustrnent of its circumference to accommodate and correspond to the particular length of the spliceless backing loop substrate is r~ d.
Similar methods can also be used in preparing a coated abrasive backing using a support structure, such as a conveyor system. Such a system would 3 0 typically use, for example, a stainless steel sleeve, in the form of a conveyor belt.

CA 02227~18 1998-01-21 W O 97/05990 PCTrUS96/12791 In this embodiment, the step of ~Icp~illg a fiber reinforced spliceless backing includes preparing the backing around the conveyor belt.
Other constructions, embo-1imen~, and features of the invention will become ~p~ellL from the following description of the drawings and p~r~.r~d embodiments.

Brief Description of the Drawing Figure 1 is a perspective view of an enlarged fragment of a coated abrasive backing made by the method of the invention with edge surfaces revealing cross-sectional detail.
Figure 2 is an enlarged fr~gment~ry cross-sectional view of a coated abrasive article made by the method of the invention.
Figure 3 is a perspective view of the major elements (without showing supporting structures) of an apparatus to practice a plerelled process for making an endless spliceless reinforced backing structure according to the present invention.

Detailed Description of the Invention Detailed descriptions of the present invention are provided herein.
Therefore, the invention is not limited to the specific formulations, arrangements, 2 0 and methods identified and described, except as limited by the claims.
Referring to Figure 1, a reinforced spliceless backing 10 is made by the method of the invention. In Figure l, backing 10 comprises an endless splicelessb~ ing loop substrate 11 to which is adherently bonded a fiber reinforcing layer14 which comprises reinforcing fibers lS which are saturated with binder 16.
2 5 Binder 16 adheres fibers l S within fiber reinforcing layer 14 and to backing substrate 11. Abrasive particles are then adhered by methods, such as described herein, to at least one of the exposed surfaces, front surface 17 or back surface 18, of backing 10, either on the side of fibers l S or spliceless backing loop substrate 11.
3 0 Binder 16 is applied to fibers lS in a liquid or flowable state and solidified after fibers l S are applied to backing substrate 1 I by techniques described in CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/lZ791 greater detail hereinafter. Alternately, binder 16 may be applied to b;~kinp substrate 1 1 and then fibers 15 are applied over binder 16. Herein, the term "liquid" refers to a material that is flowable or flowing, whereas the term "solid" or "solidified" refers to a m~t~ri 1I that does not readily flow under ambient 5 te~ .d~ lres and pleS:juleS.
Referring to Figure 2, the coated abrasive article, a ~egment of which is shown, comprises a b~rkinp; 20 having an endless spliceless b~rkin~ loop substrate 21. In this embodiment, reinforcing fibers 25 which are saturated with binder 26are placed adjacent the backing substrate 21. Over the reinforcing fibers 25, a 10 make coat 27 is first applied, then abrasive particles 28 are embedded therein. A
size coat 29 is then applied over abrasive particles 28. Figure 2 depicts the abrasive coating on the side of the baclcing having the reinforcing fibers; although it is to be understood that the abrasive coating alternatively, and preferably, can be provided on the side of backing substrate 21 opposite to the reinforcing fibers.
The length, width, and thickness of the reinforced backing can vary in imen~ion depending on the int~n~ecl end use. For example, the length of the coated abrasive belt (measured on the periphery of the belt) can be any desired length although typically the length is about 40-1000 centimeters (cm).
The tllickness of the endless spliceless ~ rolced backing 10 including 2 0 spliceless backing loop substrate 11 and reinforcing fiber layer 14, is typically between about 0.07 millimeter (mm) and about 1 cm for optimum flexibility, strength, and material conserv~tion. Further, the thickness of lehlrolced backing 10 preferably is consistent and uni:form, i.e., it should not vary by more than about +15% around the entire length of tlhe b~lckin~ 10, preferably not more than about 2 5 +5%. Although this variance refers to a variance along the thickness of the backing 10, it generally is reflected in coated abrasive material, i.e., the coated abrasive belt. A preferred method of in~l-ring minim~l variance of the backing m~t~ri~l, is to skive or lightly grind the exposed surface of binder layer 16 toprovide a smooth, flat surface by removing any high spots which may eventually 3 0 tend to reflect as imperfections in the final coated abrasive product. Preferably, care should be taken not to grind so deeply as to weaken or damage reinforcing CA 02227~18 1998-01-21 fibers or remove too much binder m~t~ri~l or else the strength of the b<qcking may be affected.
Other aspects of the invention will become more ~pa~ from the following more detailed description of the method of the invention.
In this regard, Figure 3 illustrates key components of an a~alaL,ls used in the process for making a coated abrasive backing according to the method of the invention. The fiber reinforced backing of the invention is made on an a~dlus 30. An endless spliceless backing loop substrate 3 l is applied to a temporary support structure 36 which has a cylindrical surface which col,~ onds to the circumference of the desired reinforced b~cking Typically, the circumference of the temporary support structure 36 (e.g., drum 36) is between about 25-350 cm, and the width is between about l 5- l 00 cm.
Reinforcing material, in this case in the form of fibers 37, leave an unwind station 38 and are wetted with liquid binder precursor m~t~ri~l at level winder station 39. These saturated fibers are then applied onto the spliceless b~ckin~ loop substrate 3 l . The winding procedure involves the use of a strand guide system 40 with level winder 39. In this method, drum 36 is rotated (typically 25-75 rpm) while the reinforcing fibers 37 are initially attached to the spliceless backing loop ~ulJ~Ilal~ 3 l (i.e., backing substrate 3 l) fitted to drum 36, and are pulled through the level winder 39, and are wound around the drum 36 helically or spirally across the width of the drum, such that the applied layer of the strand 4 l, upon completion of winding, is no wider than backing substrate 3 l .
It is ~l~fclled that the level winder 39 move across the width ofthe drum such that the contimlQus reinforcing fibers 37 are uniformly applied in a layer 2 5 across the width of the spliceless substrate 3 l . Thus, fiber 37 is in a helically wound pattern of a plurality of wraps in a layer within the organic polymeric binder mzltt~ri~ll, with each wrap of the strand parallel to the previous wrap of the strand. Furthermore, the individual wraps of the fiber 37 are at a constant nonzero angle relative to the parallel side edges of the backing substrate 3 l . The 3 0 reinforcing fibers are wound onto endless spliceless backing substrate 3 l with a spacing of about 2-50 strands per cm of width; although it is to be understood that CA 02227~18 1998-01-21 Wo 97/05990 PCT/US96/12791 a broader range of strand spac ing is contemplated within the scope of the invention. The spacing selected can depend on a nurnber of variables, such as the strand material(s), reinforcing strength needed as a function of the type of b~qc kin~
m~t~,ri~l selected and type of service intt?nclerl for the coated abrasive articles, 5 among others.
It is possible that several strands may be used to cover the entire width of the web backing in case that the strands have sufficient length to revolve more than once around the circumference of the b~C~ing web but are not sufficiently long to traverse the entire lateral widt]~ of the backing web.
Sufficient uncured resin is applied to the backing substrate 31 to provide a layer of resin at least above and below the reinforcing fiber material therein, i.e., on the outer surfaces and sometimes even the interior of the reinforcing m~t~rial The binder precursor material not only can be applied to the fibers before winding, but, ~ltt?rn~tively, it can be applied directly on backing substrate 31 after disposition on 15 drum 36 and before winding over the backing substrate 31 over the previously wound strands, or in any combinations of these coating procedures to provide adhesion of the reinforcing fibers 37 to the backing substrate 31.
It is preferred that the binder precursor used to coat the strands is exposed to an energy source (not shown), either thermal energy or radiation energy, to cure 2 0 of polymerize the binder precursor. Further processing may then occur such as additional curing, flexing and/or hllmi~lification. After this optional further processing, the endless spliceless backing can be converted or slit into the desired form or shape in preparation fc,r use as an abrasive article backing.
The temporary support structure 36 used in such a method is preferably a 2 5 drum, which can be made from a rigid material such as steel, metal, ceramic, a strong plastic material, or any combination thereof. The material of which the drum is made should have enough integrity such that repeated endless b~kingc canbe made without any damage to thc drum. The drum is placed on a mandrel so that it can be rotated at a controlled rate by a motor. This rotation can range anywhere 3 0 from 1 to 100 revolutions per minute (rpm) depending on the application. Thedrum is usually a rotatable one in the practice of the invention. Although, it is also CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 contemplated that the drum could be nolllol~ldble where the strand applying means is capable of traveling around the ch.;u l,re.cllce of the drum The drum can be unitary or created of segmen~.~ or pieces that collapse for easy removal of the endless, spliceless b~ckin,~
The circumference of the drum will generally correspond to the inner length (circumference) of the endless, spliceless backing loop substrate. The width of the endless, spliceless backing loop substrate can be of any value less than the width of the drum. A single endless, spliceless backing can be made on the drum, removed from the drum, and the sides can be trimmed. Additionally, the reinforced backing can be slit longitudinally into multiple reinforced b~king~ with each having a width substantially less than the original backing.
In many instances, it is pler~,lled that a release coating be applied to the periphery of the drum before the binder precursor or spliceless backing loop ~ub~lldle or any of the other components are applied. This provides for easy release of the endless, spliceless backing after the binder is solidified. In most instances, this release coating will not become part of the ~ontll~?s~, spliceless backing. If a collapsible drum is used in the preparation of a large endless, spliceless b~cking, such a release liner helps to prevent, or at least reduce, the formation of ridges in the inner surface of the reinforced backing, caused by seams 2 0 or welds in the drum surface. Examples of such release coatings include, but are not limited to, waxes, silicone waxes or fluorochemicals, or polymeric films coated with silicone waxes or fluorochemicals. It is also within the scope of this invention to use a second release coating which is placed over the final or top coating of the binder. This second release coating is typically present during the solidification of 2 5 the binder, and can be removed an~l ~ds.
Alternatively, in the ~lel~alation of a coated abrasive article of the present invention, the reinforcing fiber layer can be applied to the spliceless backing loop substrate supported around two drum rollers, which are connected to a motor for driving at least one of rollers to rotate the ~ kin~ Alternatively, the backing can 3 0 be installed around one drum roller, which is connected to a motor for rotating the backing. As the backing rotates, the a&esive layers or abrasive slurry are applied CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 by any conventional coating technique such as knife coating, die coating, roll coating, spray coating, or curtain coating. Spray coating is preferred for certain applications.
After applying the fibrous reinforcing material to the spliceless backing 5 loop substrate and curin~ the binder precursor, in this embodiment, the rçslllting backing is removed from the temporary drum, optionally ground to remove any high spots, and then the abrasive coating is applied to either of the fiber reinforcing layer or the opposite side of the spliceless backing substrate. The fiber reinforced backing should be turned inside out (everted) to expose the opposite surface of the 10 spliceless backing substrate, i.e., the side of the backing substrate opposite to the fiber reinforcing layer, if the abrasive coating is to be applied to that surface.
Either way, the fiber reinforced backing is again temporarily ~U~)Ol Led on any convenient support means such as either a drum or at least two cantilevered idler rolls for application of an abrasive slurry or abrasive coating (sequential coating of 15 make coat and abrasive particles).
If an abrasive slurry is not used, i.e., if the abrasive material is applied after a second or make adhesive la~er is applied, the abrasive grains can be electrostatically deposited onto the adhesive layer by an electrostatic coater. The drum roller acts as the ground plate for the electrostatic coater. ~ It~ tively, the 2 0 abrasive grains can be applied by mineral drop coating or magnetic coating.
Preferably, the make coat layer is solidified, or at least partially solidified,after embedding the abrasive particles, and then a size coat layer (and optionally a supersize coat) is applied. The size coat adhesive layer can be applied by any conventional method, such as roll coating, spray coating, or curtain coating. The 2 5 size coat is preferably applied by spray coating. The make and size coats layer(s) can then be fully solidified while the backing is still on the drum rollers.
Alternatively, the resulting product can be removed from the drum rollers prior to solidification of the adhesive layer(s).
Examples of the specific m~t~ employed in the method and coated 3 0 abrasive product of the invention are described in greater detail hereillarLel.

CA 02227~18 1998-01-21 The coated abrasive articles of the present invention include a fiber reinforced backing with the following properties. The reinforced backing is sufficiently heat resistant under grin~1ing conditions for which the abrasive article is int~n~led to be used such that the backing does not significantly fli~inte~rate, i.e., 5 split, break, del~min~te, tear, or a combination of these, as a result of the heat generated during a grinding, sanding, or polishing operation. The reinforced backing is also sufficiently tough such that it will not ~ignific~ntly crack or shatter from the forces encountered under grinding conditions for which the abrasive article is intended to be used. That is, it is sufficiently stiff to withstand typical 10 grinding conditions encountered by coated abrasive belts, but not undesirably brittle.
Preferably, the reinforced backings, and spliceless endless coated abrasive belts incorporating same, of the present invention are sufficiently flexible to with~t~n~l grinding conditions. By "sufficient flexibility" and variants thereof in 15 this context, it is meant that the reinforced b~kin~, and spliceless endless coated abrasive belts, will flex or bend under typical grinding conditions and return to their original shape without significant perm~nent deformation. Furthermore, forp~ d grinding applications, the reinforced backing (and the endless abrasive belt incorporating same) is capable of flexing and adapting to the contour of 2 0 workpiece being abraded, yet is sufficiently strong to transmit an effective ~rin-lin~
force when pressed against the workpiece.
Preferred reinforced backings of the present invention possess a generally uniform tensile strength in the longit~ in~l, i.e., m~hin~ direction. This is typically because the fibrous reinforcing material extends along the entire length of 2 5 the b~ in~ and there is no seam in the continuous fibrous reinforcing m~tt-.ri~l More preferably, the tensile strength for any portion of a reinforced backing tested does not vary by more than about 20% from that of any other portion of the reinforced backing structure. Tensile strength is generally a measure of the m~xil"l"" stress a material subjected to a stretching load can withstand without3 o tearing.

-W O 97/05990 PCT~US96/12791 Preferred leil~rced b~çkin~s of the present invention also exhibit d~lo~liate shape control and are sufficiently insensitive to ellviro~ ental conditions, such as humidity and temperature. By this it is meant t_at preferredleiLIrorced backings of the present invention possess the above-listed pr~ ies 5 under a wide range of environ~n~l conditions. Preferably, the reinforced b~-~king.~ possess the above-listed properties within a t~ p~,~dLul~ range of about 10-30~C, and a humidity range of about 30-90% relative hl-mi(li~y (RH). More preferably, the reinforced b7lcking.~ possess the above-listed properties under a wide range of temperatures, i.e., from below 0~C to above 1 00~C, and a wide range of humidity values, from below 10% RH to 100% RH.
The reinforced h~king~ should also be able to with.ctsln~l the grinding conditions and environments to which the coated abrasive article product is intended.

15 Backin~ Substrate The preferred backing substrate material used in coated abrasive ba~ inp.
of the present invention is generally chosen such that there will be compatibility with, and good adhesion to, the adhesive layers, particularly to the make coat.
Good adhesion is determined by the amount of ".~helling" of the abrasive m~t~.ri~l 2 0 Shelling is a term used in the abrasive industry to describe the undesired, premature release of a significant amount of the abrasive m~t~ri~l from the backing. Although the choice of backing substrate m~tçri~l is important, the amount of ~hçlling typically depends to a greater extent on the choice of adhesive and the comp~tihility of the backin~: substrate and adhesive layers and grinding2 5 conditions.
The backing substrate is comprised of an endless, spliceless (tube-like) backing substrate. The backing substrate is then reinforced by continuously wound fibrous material, such as yarn, to provide the backing described herein.
The endless spliceless backing loop ,ubslldle is generally selected from the 3 0 group con.~i~ting of a polymeric film (including primed polymeric film), a woven CA 02227~18 1998-01-21 cloth, a knitted cloth, paper, a vulcanized fiber substrate, a nonwoven, including combinations and treated versions thereof.
The plc;re~led endless backing substrate is a cloth backing, either woven or knitted. Examples of materials useful as endless spliceless backing loop substrates in this inventio n include polyester, nylon, rayon, cotton, jute, and other m~tP.ri~7l.c know as cloth b~ckin~ The cloth is composed of yarns in the warp direction, i.e., the m~7~hine direction, and yarns in the fill direction, i.e. the cross direction. The cloth backing substrate can be a woven backing, a stitchbonded b~c7~in~ or a weft insertion b~cking Examples of woven constructions include sateen weaves of 4 over one weave of the warp yarns over the fill yearns; twill weave of 2 or 3 over one weave; plain weave of one over one weave, and a drill weave of two over two weave. In a stitchbonded fabric or weft insertion backing, the warp and fill yarns are not interwoven, but are oriented in two distinct directions from one another.
The warp yarns are laid on top of the fill yarns and secured to another by a stitch yarn or by an adhesive. The endless spliceless backing is generally a tubular backing, me~ning there can be found no appreciable beginning or end.
Endless spliceless backing loop substrates are available from suppliers such as, for example, Advanced Belt Technology (of Middletown, CT) under the ~lç~ign~ti(7ns "WT3" and "WT4", and other various cloth m~nl7f~cturers.
2 0 The yarns in the cloth backing substrate can be natura., synthetic or combinations thereof. Examples of natural yarns include cellulosic yarns such ascotton, hemp, kapok, flax, sisal, jute, carbon, manila, and combinations thereof.
Examples of synthetic yarns include polyester yarns, polypropylene yarns, glass yarns, polyvinyl alcohol yarns, polyimide yarns, aromatic polyamide yarns, rayon2 5 yarns, nylon yarns, polyethylene yarns and combinations thereof. The p~ ed yarns of this invention are polyester yarns, nylon yarns, a mixture of polyester and cotton, rayon yarns, and aromatic polyamide yarns.
The cloth backing substrate can be dyed and/or stretched, (~e~i7.e-l, washed, or heat stretched. Additionally the yarns in the cloth backing can contain primers, 3 0 dyes, pigments or weKing agents. The yarns can be twisted or text7~red.

-:
CA 02227~18 1998-01-21 W 097/05990 PCTrUS96/12791 Polyester yarns are ffilme~ from a long chain polymer made fTom the reaction of an ester of dihydric alcohol and terephthalic acid; preferably this polymer is a linear polymer of poly(ethylene terephth~l~t~?). There are three main types of polyester yarns: ring spuln, open end and filament. A ring spun yarn is5 made by continuously drafting a polyester yarn, twisting the yarn and winding the yarn on a bobbin. An open end yarn is made directly fTom a sliver or roving. A
series of polyester rovings are opened and then all of the rovings are continuously brought together in a spinning ~pal~Lus to form a continuous yarn. A filament yarn is a long continuous fiber; a fil~ment yarn typically has a very low or non-10 existent twist to the polyester fiber.
The denier of the fibers should be less than about 5000, preferably betweenabout lO0 to lS00. The yarn size should range fTom about lS00 to 12,000 meters,~kilogram. For a coated abrasive cloth backing, the weight of the greige cloth, i.e., the untTeated cloth, will range fTom about O.lS to l kg,'m2, preferably between about 0.15 to 0.75 kg,tm2.
The backing substrate may have an optional s~ l resin coat, presize coat and,~or backsize coat. If the backing substrate is a cloth backing ~ul~ dl~, at least one of these coats is required. The purpose of these coats is to seal the backing substTate and,~or protect the yarns or fibers in the backing substTate. The addition 2 0 of the presize coat or b~ckci7~ coat may additionally result in a "smoother" surface on either the fTont or back side of the backing substTate. The presize or b~ i7~coat may penetTate through the entire thickness of the backing substTate, or may be applied so that the coating only penetrates half of the substrate thickness. Thedepth of penetTation can be controlled by the viscosity of the various coatings.2 5 Viscosity can be altered, for exarnple, by silica or clay additions.
After any one of the sdluld~ll coat, backsize coat or presize coat is applied tothe backing substrate, the resulting backing substrate can be heat tTeated or calendered. The heat treating can be done as the binder precursor is at least partially solidified by placing the backing substTate in a tenter fTame which is in an 3 0 oven. Additionally the backing substrate can be processed through heated hot CA 02227~18 1998-01-21 cans. The calendering step will remove some surface roughn~ss and typically increase the surface smoothness.
Fx~mples of latex resins that can be mixed with the phenolic resin to treat the cloth backing include acrylonitrile butadiene emulsions, acrylic emulsions, 5 butadiene emulsions, butadiene styrene emulsions and combinations thereof.
These latex resins are commercially available under various tr~(1en~nnes from a variety of different sources including: "RHOPLEX" and "ACRYLSOL"
commercially available from Rohm and Haas Company, "FLEXCRYL" and "VALTAC" commercially available from Air Products & Chemicals Inc., 10 "SYNTHEMUL" and "TYLAC" commercially available from Reichold Chemical Co., "HYCAR" and "GOODRITE" commercially available from B.F. Goodrich, "CHEMIGUM" commercially available from Goodyear Tire and Rubber co., "NEOCRYL" commercially available from ICI, "BUTAFON" commercially available from BASF, and "RES" commercially available from Union Carbide.
The b~cking substrate may additionally comprise other optional m~t~?ri~
such as additives selected from the group consisting of fillers, fibers, ~ntiet~tic agents, lubricants, wetting agents, sllrf~ct~nt~, pigments, dyes, coupling agents, plasticizers, and suspending agents, such as those described for ba(~lfinF~ in PCT
Published Application No. WO 93/12911 published 8 July 1993 (Benedict et al.).
2 0 The amounts of these m~tt-ri~l~ are selected to provide the properties desired.

Fibrous Reinforcin~ Material The fibrous reinforcing material used in the invention to reinforce the spliceless backing loop substrate preferably is in the form of individual f1brous 2 5 strands. Alternatively, the material can be a narrow fibrous strip having a lateral width less than that of the backing substrate, such as in a preferred ratio of 1/100 to 10/100.
Suitable fibrous strands for this invention are commercially available as threads, cords, yarns, rovings, and fil~nnent~ Threads and cords are typically 3 0 assemblages of yarns. A thread has a very high degree of twist with a low friction surface. A cord can be assembled by braiding or twisting yarns and is generally CA 02227~18 1998-01-21 larger than a thread. A yarn i,s a plurality of fibers or fil~ment.s either twisted together or entangled. A roving is a plurality of fibers or filaments pulled together either without a twist or with minim~l twist. A filament is a continuous fiber.
Both roving and yarns are composed on individual fil~rnent.~ A fiber mat or web 5 consists of a matrix of fibers, i.e., fine thread like pieces with an aspect ration of at least about 100:1. The aspect ratio of a fiber is the ratio of the longer tlimen~ion of the fiber to the shorter ~limen~ion.
In general, the fibrous reinforcing material can be composed of any m~t~ri~l that increases the strength of the backing and/or prevents stretch. Examples of 10 useful reinforcing fibrous m~teri~l in applications of the present invention include metallic or nonmetallic fibrous m~teri~l, with the ~ler."led being nonmetallic. The nonmetallic fibrous materials xnay be m~f~ri~l~ made of glass including "FIBERGLAS", carbon minerals, synthetic or natural heat resistant organic reinforcing materials, or ceramic m~t~ri~l~ Prefenred fibrous lehlrolcil~g m~tt-ri~lc 15 for the present invention are organic m~teri~l~, glass, and ceramic fibrous mzlt~ri~l Useful natural organic fibrous materials include wool, silk, cotton, or cellulose.
Examples of useful synthetic organic fibrous materials are made from polyvinyl alcohol, nylon, polypropylene, polyester, rayon, polyamide, acrylic, polyolefin,ararnid, or phenol. The prefened organic fibrous m~teri~l for applications of the 2 0 present invention is aramid fibrous m~teri~l; such a material is commercially available fron1 DuPont Co. under tlle trade names of "KEVLAR" and "NOMEX".
It is also possible to have more than one type of reinforcing fiber in the backing construction. Generally, any ceramic fibrous reinforcing material is useful in applications of the present invention. An example of a ceramic fibrous reinforcing 2 5 material suitable for the present invention is "NEXTEL" is commercially available from The 3M Company.
It is possible to use mo]re than one type of reinforcing fiber in this construction. Dirrel~l-t fibers, such as "FIBERGLAS" and nylon, or "FIBERGLAS" and polyester, or aramid and nylon, or aramid and polyester, can 3 0 be used in combination as the types of strand material by alternate winding of each type across the width of the preformed spliceless b~cking, either in the same CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 winding direction or in a criss-cross type winding. The dirr~ ll fibers used should be chosen for their desirable properties, such as low stretch for fiberglass and high strength for nylon. It is also possible to co-twist 2 or more strands together, the strands being the same or different in any of composition, denier, twist and so forth, and then apply the resulting yarn to the spliceless backing as a single strand.
The dirr~ strands can be selected to contribute dirr~ l desired physical properties to the composite co-twisted fiber to provide a balance of plo~,l lies.
The reinforcing fibers may contain a pretreatment of some kind, prior to being incorporated into the backing. This ~leLle;.~ ent may be an adhesion promoter or a sl~hing compound. For example, the fiberglass reinforcing fibers may contain a surface tre~tment, such as an epoxy or urethane compatible fiberglass yarn to promote adhesion to the make coat. Examples of such fiberglass yarns are "930" fiberglass yarns from PPG, Pi~lsl)ul~,ll, PA, and "603" fiberglass yarns from Owens-Corning. Useful grades of such glass yarns and rovings are in the range of about 150 to 32,000 meters/kg, which are also preferred.
If glass fibrous reinforcing material is used, it is ~ler~ d that the glass fibrous material be accompanied by an interfacial binding agent, i.e., a coupling agent, such as a silane coupling agent, to improve a&esion to the organic bindermslteri~l, particularly if a thermoplastic binder material is used. Examples of silane 2 0 coupling agents include "Z-6020" or "Z-6040" both available from Dow Corning Corp.
It is required that the fibrous reinforcing material is of a length sufficient to extend around the length, i.e., circumference, of the coated abrasive loop a plurality of times and provide at least one distinct layer of fibrous lchlrorcillg m~tPri~l In 2 5 other words, the fibrous reinforcing m~teri~l is of a length sufficient to place the strand in a helically wound pattern of a plurality of wraps in a layer within the organic polymeric binder material, with each wrap of the strand parallel to and in contact with the previous wrap of the strand. This helix generally and preferably extends longitudinally along the entire length of the backing loop. That is, each 3 0 wrap of the strand approaches a parallel position relative to the side edges of the loop, although no individual wrap exactly parallels the side edges. Rather, the CA 02227~18 1998-01-21 W O 97/O~99O PCT~US96/12791 wraps are preferably at a constant, substantially nonzero angle relative to the parallel side edges of the spliceless backing substrate or web.
The Leinrolcillg fiber dlenier, i.e., degree of fineness, for pl~rell~d fibrous reinforcing m~teri~l ranges from about S to about 5000 denier, typically betweenabout 50 and about 2000 denier. More preferably, the fiber denier will be bGLwGell about 100 and about 1500. It is understood that the denier is strongly influenced by the particular type of fibrous reinforcing material employed.
It is possible in this invention that there are provided distinct regions of thebacking (spliceless backing loop substrate/reinforcing layer) that do not have fibrous reinforcing material therein. This results in one area of the backing having a greater ratio of fibrous reinforcing material to organic polymeric binder m~t~ri~
than another area. For example, the fibrous reinforcing material can be entirelylocated within a region in the lateral sides and/or the central area of the backing layer such that some outer edges thereofwould be subst~nti~lly uncovered by fibrous reinforcing m~teri~l I'his embodiment may not be acceptable in all casesas it may create an uneven surface on the b~r.kin~
In reinforcing the backing substrate, the fibrous reinforcing material is applied onto the spliceless backing loop substrate which is temporarily held on a support structure described herein, such as a drum structure. The binder precursor 2 0 can be applied first to the spliceless backing loop substrate, followed by winding of the reinforcing material. Alternatively, the reinforcing material can be applied first to the spliceless backing loop substrate, followed by the binder precursor. In athird embodiment, the reinforcing material can be first saturated with the binder precursor and then applied to the spliceless backing loop substrate. Thus, the 2 5 binder precursor can be applied sequentially or .simlllt~neously with the reinforcing m~teri~l. It is also within the scope of this invention to use a combination of any of these three previous methods.
It is also within the scope of the invention to use a nonwoven substrate in combination with the reinforcing fibers. The nonwoven substrate, in some 3 o instances, can increase the tear strength of the resulting backing. It is collL~ lated for instance, that a nonwoven substrate is first saturated with a first binder CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 precursor and applied over the second surface of the backing substrate. Next, the reinforcing yarns are applied on top of the saturated nonwoven substrate. The first binder precursor will wet the reinforcing yarns and bond the reinforcing yarns to the backing substrate.
In one aspect of the invention, the reinforcing fibers are applied to an endless spliceless backing loop substrate already Cont~ining an abrasive coating.
In this aspect, the backing substrate is turned inside out, i.e., the abrasive coating faces the support drum and the reinforcing fibers are applied to the backing substrate surface opposite the abrasive coating. After the reinforcing fibers are applied and the binder precursor is solidified, the resulting endless belt is essentially turned inside out to form the endless coated abrasive article.
The resulting endless abrasive belt article of the invention comprises a backing having a spliceless backing loop substrate and a plurality of reinforcing fibers continuously present over the surface area. It is generally pl~re.l~d that the reinforcing fibers be parallel and non-interlacing as applied upon the backing substrate. It is also within the scope of this invention that the reinforcing fibers are continuous over the entire lateral width of the spliceless backing loop substrate, i.e., there is no substantial break or gap in the spacing of the reinforcing fibers across the width of the backing substrate. It is understood that the reinforcing fiber 2 0 will have a starting end and a tail end with the intervening length of the fiber continuous in at least more than one revolution around the spliceless backing loop substrate.
While the use of pl~ro,l"ed fibers are preferred as the fibrous reinforcing m~t~ri~l, the use of monofilament thermoplastic and thermoelastic beads extruded2 5 and cooled in-situ as helical windings over the spliceless backing substrate are also contemplated.

Binder Precursor Material for Reinforcin~ Fibers The binder precursor material used for securing the fibrous reinforcing 3 0 material strands or narrow strips can be selected from a wide variety of binder materials which can be applied in liquid form and later solidified. Typically, the CA 02227~18 1998-01-21 W 097/05990 PCT~US96/12791 amount of binder precursor, which is an organic polymeric binder m~tt-ri~l, used to saturate the reinforcing fibers is within a range of about 40-99 wt%, more preferably within a range of about 65-92 wt%, and most preferably within a rangeof about 70-85 wt%, based on the total weight of the fiber reinforcing layer alone.
The binder m:~t~ri~l used to secure the reinforcing m~t~ 1 in the fiber reinforcing layer is an organic polymeric binder m5lt~ri~1 It can be a cured or solidified thermosetting resin, therrnoplastic material, or elastomeric m~t~risll Preferably, the organic polymeric binder material is a cured or solidified thermosetting resin. It is preferred that the binder material is a thermosetting resin, at least because such resins can be provided in a very fluid (low viscosity) flowable form when uncured, even under ambient conditions. Herein, the phrase "ambient conditions" and variants thereof refer to room temperature, i.e., 1 ~-30~C, generally about 20-25~C, and 30-50% relati~e humidity, generally about 35-45% relative humidity.
If the organic polymeric binder material of the backing includes a curable thermosetting resin, prior to the m~nllf~cture of the backing, such as for wetting the reinforcing fibers 15 and/or for imprçgn~ting a cloth backing web 11 with a binder precursor, the thermosetting resin is in a nonpolymerized state, typically in a liquid or semiliquid state. During the m~nllf~turing process, the thermosetting resin is 2 0 cured or polymerized to a solid state. Depending upon the particular thermosetting resin employcd, the thermosetting resin can use a curing agent or catalyst. Whenthis curing agent is exposed to an al,~Lopliate energy source (such as thermal energy or radiation energy) the curing agent will initiate the polymçri7~fion of the thermosetting resin.
2 5 Examples of thermosetting resins from which the backing can be pL~cd include phenolic resins, amino resins, polyester resins, aminoplast resins, urethane resins, melamine-formaldehyde resins, epoxy resins, acrylated iso~;y~l~dte resins, urea-formaldehyde resins, acrylate resins and mixtures of isocyanurate resins, acrylated urethane resins, acry]ated epoxy resins, or mixtures thereof. The 3 0 preferred thermosetting resins are urethane resins, acrylate resins, epoxy resins, acrylated urethane resins, polyester resins, or flexible phenolic resins, and lni~ S

CA 02227~18 1998-01-21 WO 97/05990 PCT~US96/12791 thereof. The most l~rert;llcd resins are urethane resins, acrylate resins, epoxyresins, acrylated urethane resins, and mixtures thereof, because they exhibit anacceptable cure rate, flexibility, good thermal stability, strength, and water resistance.
One ~ler~ d class of binder m~teri~l is polyul~lhalle elastomer, in particular a polyether based polyul~Lhane. Examples of such polyurethane m~tçri~ls are commercially available from Uniroyal Chemical under the trade ~lc~ign~tion "VIBRATHANE" and "ADIPRENE". These polyurethane elastomers are formed from prepolymers that can be a polyether based upon toluene diioscyanate termin~tPd prepolymer or a polyether based upon diphenylmethane diisocyanate. These prepolymers can be crosslinked with 4,4'-methylene-bis-(ortho-chloroaniline) or a diamine curative. The polyurethane binders are also e.l~d, because during thermal curing the polyurethane resins do not appreciably reduce their viscosity and thus do not appreciably flow during curing.
It is also within the scope of this invention to blend polyul~lh~le resins with epoxy resins and acrylate resins.
Phenolic resins are usually categorized as resole or novolac phenolic resins.
Examples of useful commercially available phenolic resins are "VARCUM" from BTL Specialty Resins Corporation; "AROFENE" from Ashland Chemie~l 2 0 Company; "BAKELITE" from Union Carbide; and "RESINOX" from Monsanto Chemical Company.
Resole phenolic resins are characterized by being :~lk~line catalyzed and having a molar ratio of formaldehyde to phenol of greater than or equal to 1:1.
Typically, the ratio of formaldehyde to phenol is within a range of about 1:1 to2 5 about 3 :1. Examples of ~Ik~line catalysts useable to prepare resole phenolic resins include sodium hydroxide, potassium hydroxide, organic amines, or sodium carbonate.
Novolac phenolic resins are characterized by being acid catalyzed and having a molar ratio of form~l~lehyde to phenol of less than 1:1. Typically, the3 0 ratio of formaldehyde to phenol is within a range of about 0.5 :1 to about 0.8:1.
Examples of the acid catalysts used to prepare novolac phenolic resins include sulfuric, hydrochloric, phosphoric, oxalic, or p-tohl~n~slllfonic acids. Although novolac phenolic resins are typically considered to be thermoplastic resins rather than thermosetting resins, they can react with other chemicals (e.g., he~methylenetetraamine) to form a cured thermosetting resin.
Epoxy resins useful in the polymeri7~ble mixture used to prepare b~rlrin of this invention include monomcric or polymeric epoxides. Useful epoxy mzlt~ri~l.s, i.e., epoxides, can vary greatly in the nature of their backbones and s~lbstit~7ent groups. Representative examples of acceptable substituent groups include halogens, ester groups, ether groups, sulfonate groups, siloxane groups,nitro groups, or phosphate groups. The weight average molecular weight of the epoxy-cf nt~inin~ polymeric materials can vary from about 60 to about 4000, and are preferably within a range of about l 00 to about 600. Mixtures of various epoxy-c~-nt~inin~ mzt(~riz~l~ can be used in the compositions of this invention.Examples of commercially available epoxy resins include "EPON" from Shell Chemical Co.; and "DER" from Dow Chemical Company.
Examples of commercially available urea-fonn~kl~hyde resins include "UFORMITE" from Reichold Chemic~l, Inc.; "DURITE" from Borden Chemic~l Co.; and "RESIMENE" from Monsanto. Examples of commercially available mel~mine-formaldehyde resins include "UFORMITE" from Reichhold Ch~mic~l, 2 0 Inc. NC; and "RESIMENE" from Monsanto. "RESIMENE" is used to refer to both urea-formaldehyde and melarnine-formaldehyde resins.
Examples of aminoplast resins useful in applications according to the present invention are those having at least one pendant alpha, beta-ull~dluldledcarbonyl groups per molecule, which are disclosed, for example, in U.S. Patent 2 5 Nos. 4,903,440 (Larson et al.) and 5,236,472 (Kirk et al.).
Useable acrylated iso~.y~~ resins are those prepared from a mixture of:
at least one monomer selected from the group c~ n~icting of iso~;y~luldle derivatives having at least one t~nin~l or pendant acrylate group and isocyanatederivatives having at least one terminal or pendant acrylate group; and at least one 3 0 aliphatic or cyclo~lirh~tic monomer having at least one terminz~l or pendant CA 02227~18 1998-01-21 acrylate group. These acrylated isocy~wale resins are described, for example, inU.S. Patent No. 4,652,274 (Boettcher et al.).
Ethylenically unsaturated resins include both monomeric and polymeric compounds that contain atoms of carbon, hydrogen and oxygen, and optionally, nitrogen and the halogens. Oxygen or nitrogen atoms or both are generally present in ether, ester, urethane, amide, and urea groups. Ethylenically unsaturated compounds preferably have a molecular weight of less than about 4,000 and are preferably esters made from the reaction of compounds cont~ining aliphatic monohydlo~y groups or aliphatic polyhydroxy groups and unsaLul~ed carboxylic 1 0 acids, such as acrylic acid, methacrylic acid, itaconic acid, crotonic acid, isocrotonic acid, maleic acid, and the like. Representative examples of acrylateresins include methyl methacrylate, ethyl methacrylate styrene, divinylbenzene, vinyl toluene, ethylene glycol diacrylate, ethylene glycol methacrylate, hexslnerliol diacrylate, triethylene glycol diacrylate, propyleneglycol diacrylate, trimethylolpropane triacrylate, glycerol triacrylate pentac~yLlllilol triacrylate, pentae~yLllliLol methacrylate, tetraacrylate. Other ethylenically unsaturated resins include monoallyl, polyallyl, and polymethallyl esters and diallyl ~f1ip~t~, and N,N-diallyl~lip~mide. Still other nitrogen co-,L~ g compounds include tris(2-acryloyl-oxyethyl) isoey~lwdLe, 1,3,5-tri(2-methylacryloxyethyl)-s-tri~7int?, 2 0 acrylamide, methlacrylamide, N-methylacrylamide, N-N-dimethylacrylamide, N- vinylpyrrolidone, and N-vinylpiperidone.
Acrylate urethanes are diacrylate esters of hydroxy t~rrnin~te.d NCO
çxt~nded polyesters or polyethers. Fx~rnples of commercially available acrylatedurethanes include "WITHANE 782", available from Morton Thiokol Chl~n ic~l, and "CMD 6600", "CMD 8400", and "CMD 8805", available from Radcure Specialties.
The acrylated epoxies are diacrylate esters, such as the diacrylate esters of bisphenol A epoxy resin. Examples of commercially available acrylated epoxies include those having the trade names "EBECRYL 3500", "EBECRYL 3600", and 3 0 "EBECRYL 8805", available from Radcure Specialties.

CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 Suitable thermosetting polyester resins are available as "E-737" or "E-650"
from Owens-Corning Fiberglass Corp. Suitable polyulcLllalles also are available as "VIBRATHANE" B-8 13 preplolymer or "ADIPRENE" BL-16 prepolymer used with "CAYTUR"-3 1 curative. All are available from Uniroyal Chemi~ ~l As indicated previously, in some applications of the present invention, a thermoplastic binder material can be used to bond the reinforcing fibers wound to the backing substrate, as opposed to the pler~ ed thermosetting resins discussedabove. A thermoplastic binder m~teri~l is a polymeric m~ten~l that softens when exposed to elevated temperatures and generally returns to its original physical state when cooled to ambient temperatures. During the m~nnf~cturing process, the thermoplastic binder is heated above its softening temperature, and often above its melting temperature, to be in a flowable state. After the reinforced fibers are bonded to the backing substrate, the thermoplastic binder is cooled and solidified.
Preferred thermoplastic ma~erials of the invention are those having a high melting temperature and/or good heat resistant properties. That is, ~rt;r~,.lGd thermoplastic m~t.?ri~l~ have a melting point of at least about 1 00~C, preferably at least about 150~C. Additional]y, the melting point ofthe ~l~r~ d thermoplastic m~t~ri~l~ is sufficiently lower, i.e., at least about 25~C lower, than the melting L~ ldlule of the reinforcing m aterial. In this way, the reinforcing m~t~ l is not 2 0 adversely effected during the meltil1g process of the thermoplastic binder.Examples of thermoplastic m~teri~l~ suitable for ~i~aldlions of b~cking~
in articles according to the present invention include polyca In~lldles, polyetherimides, polyesters, polysulfones, poly~Lylenes, acrylonitrilebutadiene-styrene block copolymers, polypropylenes, acetal polymers, poly~mi~1ec, polyvinyl 2 5 chlorides, polyethylenes, polyurethanes, or combinations thereof. Of this list, polyamides, polyurethanes, and polyvinyl chlorides are ~ler~lled, with polyurethanes and polyvinyl chlorides being most pl~r~ d.
If the thermoplastic material from which the backing is formed is a polycarbonate, polyeth~rimicle, polyester, polysulfone, or polystyrene material, a 3 0 primer can be used to enhance the adhesion between the fiber l~h-folcillg layer and the make coat, if the make coat is chosen to be applied on that side of the backing.

CA 02227~18 1998-01-21 The terrn "primer" is meant to include both mechanical and ch-omi~l type primersor priming processes. This is not meant to include a layer of cloth or fabric attached to the surface of the backing. Examples of mechanical primers include, but are not limited to, corona treatment and scuffing, both of which increase the 5 surface area of the surface. An example of a chemical primer is a colloidal dispersion of, for example, polyurethane, acetone, a colloidal oxide of silicon,is~ pallol, and water, as disclosed, for example, by U.S. Patent No. 4,906,523 (Bilkadi et al.).
Although priming of a surface can involve scuffing, i.e., ronghening up to 10 increase the surface area of the surface, the surface of the backing is still relatively "smooth" as defined above. That is, the surface topology is generally smooth andflat such that there is little, if any, exposed, i.e., protruding, fibrous reinforcing material. Preferably, the surface topology is generally not effected by the fibrous reinforcing m~teri~l within the organic polymeric binder material such that it 15 would mirror the underlying topology of the fibrous reinforcing mz~terizll A third type of binder useful in the 7~ Lillg the reinforcing fibers of the present invention is an elastomeric m~t~ri~l An elastomeric m~teri~l, i.e., elastomer, is defined as a material that can be stretched to at least twice its original length and then retract very rapidly to approximately its original length, when 2 0 released. Examples of elastomeric materials useful in applications of the present invention include styrene-bllt~liene copolymers, polychloroprene (neoprene), nitrile rubber, butyl rubber, polysulfide rubber, bis- 1 ,4-polyisoprene, ethylene-propylene terpolymers, silicon rubber, or polyurethane rubber. In some in~t~n~e~, the el~tomeric materials can be crosslinked with sulfur, peroxides, or similar 2 5 curing agents to form cured therrnosetting resins.
Care should be taken to monitor the viscosity of the binder m~t~ri~l during its application to the reinforcing fiber strands. If the viscosity of the binderprecursor is too low, then during further processing of the abrasive article, the binder precursor will tend to flow or "run". This flow is undesirable and may cause 3 0 the placement and orientation of the reinforcing fibers to shift. On the other hand, if the viscosity of the binder precursor is too high, then the binder precursor may CA 02227~18 1998-01-21 not adequately wet the reinforcin~ fibers. A pler~lled viscosity range is between about S00 to 20,000 centipoise, more preferably between 1,000 and lS,000 and nnost preferred between 2,000 to 10,000 centipoises. These viscosity measurements are taken at room temperature. The viscosity may be adjusted by 5 the amount of solvent (the % solids of the resin) and/or the ch~mi~t y of the starting resin.
Heat may additionally be applied during the applying of the l~h,roicillg strands to the spliceless b~-~kin~ substrate on the t~ pOl~l y support to effect better wetting of the binder precursor onto the reinforcing fibers. However, the arnount 10 of heat should be controlled such that there is not premature solidification of the binder precursor.
The binder preferably should substantially engulf or encase the ~ roLeillg fibers. The binder precursor will ~vet the majority of the reinforcing fibers, however there may be a minor, preferably a very minor amount of reinforcing 15 fibers that are not engulfed by the binder precursor. There should be sufficient binder to substantially fill in any gaps or spaces between the reinforcing fibers, although at times it may be desired that some texture remains. The term "sufficient" means that there is enough binder precursor to provide an abrasive backing that has the desired properties for the intt?ntled application. These 2 0 properties include tensile strength, heat resistance, tear resistance, stretch, and the like. There rnay be sufficient binder within a backing, and still have some in~rn~l porosity. Again, however, it is preferred that this internal porosity be minimi7~r1 Additionally, the binder will typically seal the back side of the backing to provide an continuous layer or coating on the back side of the spliceless backing substrate.
2 5 The term seal means that a liquid, such as water, cannot penetrate into the backing through the back side of the backing.
Typically, the binder precursor is solidified by exposure to an energy source, such as thermal energy or radiation energy. The fiber reinforced backingstructure can be rotated on the drum during thermal curing. This rotation can 3 o minimi7~ the binder precursor fron[l flowing during its curing to form a nonsmooth CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 contour, and thus ultimately minimi7~s the shifting of abrasive particles if later applied to the fiber reinforcing layer during a curing of a make coat.
One preferred method of making the l~hl~lced backing structure of the invention is to first provide an endless spliceless backing loop substrate which has the length of the final desired belt length; this backing is then removably applied to a support structure or drum. Alt~rn~ting yarns or strands of nylon and fiberglass then are applied over the spliceless backing substrate by winding techniques described hereinabove. Alternatively, the two different types of fibers can be polyester and ararnid. As the yarns are applied, the tension should be set such that the yarns are pulled down onto the spliceless backing substrate. This tension will also help promote wetting of the binder precursor onto the reinforcing yarns.
There is sufficient binder precursor used to at least wet the reinforcing yarns before, during or after their application to the surface of the b~c~ing substrate.
In some instances, to make a uniform backing, the fibrous l~hlfolcillg material is applied in two wound layers, these two layers having windings which cross in inclination. It is preferred that after the first winding is applied, the binder precursor is at least partially cured before a second winding (including additional binder precursor) is applied.
In one further optional embodiment of the invention, garnet, silica, polymer 2 o particles, or coke particles, and the like, can be dispersed, such as by electrostatic coating, slurry coating, drop coating, or spray coating, in a resin akin to that used to wet the fibrous reinforcing strands. This dispersion can be coated onto either the exposed side of the backing substrate or the fiber reinforcing layer, whichever side is opposite to the side l1ltim~tely bearing the abrasive co~ting, to impart texture to 2 5 provide a frictional grip coat or traction coat. This traction coat can facilitate the driving of the belt. The traction coat also could be formed of a binder precursor with mineral particles or fibers dispersed therein, or woven or nonwoven webs.

Abrasive Coatin~
3 0 The reinforced backing structure, comprising a spliceless backing loopsubstrate and the fibrous reinforcing material applied thereover as described herein, CA 02227~18 1998-01-21 is then used as a coated abrasive backing. The abrasive m~t~ri~l can be applied by any known means, i.e., drop coating, slurry coating, electrostatic coating, rollco~tin~, etc. The abrasive coating is preferably applied to the side of the b~cking having the spliceless conventi- n~l backing due to the increased adhesion to ffle 5 conventional backing over the fibers.
Once the fiber reinforced backing is formed, the introduction of abrasive particles and several adhesive layers, which are typically also applied in binder precursor form, is contemplated in the context of forming the abrasive coating surface of the article.

Make Coat A make coat, or second adhesive layer, can be applied to either side of the ba~ ing, the spliceless backing substrate side or the reinforcing fiber layer side, however the spliceless backing substrate side is ~L~r~ d. The make coat binder 15 precursor can be coated by any conventional technique, such as knife co~ting~ spray coating, roll coating, rotogravure coating, and the like.
The composition of the adhesive layers which relate to the make coat and the size and supersize coats mentioned below, can be the following mzlt~
The adhesive layers in the coated abrasive articles of the present invention 2 0 used variously as make, size and ~u~ ize coats, typically are formed from a resinous adhesive. Each of the layers can be formed from the same or dirr~le~l~
resinous adhesives. Useful resinous adhesives are those that are compatible withthe organic polymeric binder rn~teri~l of the backing. Cured resinous adhesives are also tolerant of grin(1ing condiitions such that the adhesive layers do not deteriorate 2 5 and prematurely release the abrasive m~t~ri~l The resinous adhesive is preferably a layer of a thermosetting resin.
Examples of useable thermosetting resinous adhesives suitable for this inventioninclude, without limitation, phenolic resins, aminoplast resins, urethane resins, epoxy resins, acrylate resins, acrylated isocyanurate resins, urea-formaldehyde 3 o resins, isocy~lul~Le resins, acrylated urethane resins, acrylated epoxy resins, or ~ Lules thereof.

CA 02227~18 1998-01-21 Preferably, the therrnosetting resin adhesive layers contain a phenolic resin, an aminoplast resin, or combinations thereof. The phenolic resin is preferably aresole phenolic resin. Fx~mrles of commercially available phenolic resins include "VARCUM" from OXY Chem Corporation, Dallas, TX; "AROFENE" from 5 Ashland Chemical Co~ any, Columbus, OH; and "BAKELITE" from Union Carbide, Danbury, CT. A pl~ef~.led atninoplast resin is one having at least one pendant alpha, beta-unsaturated carbonyl groups per molecule, which is made according to the disclosure of U.S. Patent No. 4,903,440 (Larson et al.) or 5,236,472 (Kirk et al.).
The make and size coats, layers 27 and 29 respectively in Figure 2, can preferably contain other m~teri~l~ that are commonly utilized in abrasive articles.
These materials, referred to as additives, include grinding aids, fillers, coupling agents, wetting agents, dyes, pigment~, plasticizers, release agents, or combinations thereof. One would not typically use more of these materials than needed for 15 desired results. Fillers are typically present in no more than an arnount of about 90 wt%, for either the make or size coat, based upon the weight of the adhesive.
Examples of useful fillers include calcium salts, such as calcium carbonate and calcium metasilicate, silica, metals, carbon, or glass.
Preferably, the adhesive layers, at least the make and size coat, the second 2 0 and third adhesive layers, respectively, are formed from a calciutn met~ilicate filled resin treated with a silane coupling agent, such as resole phenolic resin, for example. Resole phenolic resins are preferred at least because of their heat tolerance, tollghn~ss, high hardness, and low cost. More preferably, the a&esivelayers include about 50-90 wt% silane treated calcium metasilicate in a resole 2 5 phenolic resin.

Abrasive Particles The abrasive particles suitable for this invention include fused al..,..i~.l....oxide, heat treated alllmin~lm oxide, cerarnic alllminllm oxide, silicon carbide, 3 0 alumina zirconia, garnet, diarnond, cubic boron nitride, lil~iulll diboride, or Lules thereof. The abrasive particles can be either shaped (e.g., rod, triangle, o , CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 pyramid) or unshaped (i.e., irregular). The term "abrasive particle" encomp~.cesabrasive grains, agglomerates, or multi-grain abrasive granules. Exarnples of such agglomerates are described in U.S. Patent No. 4,652,275 (Bloecher et al.) and U.S.
Application No. 08/316,259 (Chr~ti~n~on) filed 30 September 1994 and ~ign~l to the assignee of the present invention. The agglomerates can be irregularly shaped or have a precise shape associated with them, for example, a cube, pyramid, truncated pyramid, or a spher,e. A~ agglomerate comprises abr~ive particles or grains and a bonding agent. The bonding agent can be organic or inorganic.
Examples of organic binders iinclude phenolic resins, urea-fonn~ yde resins, 1 0 and epoxy resins. Example of inorganic binders include metals (such as nickel), and metal oxides. Metal oxides are usually classified as either a glass (vitrified), ceramic (crystalline), or glass-ceramic. Further information on ceramic agglomerates is disclosed in U.S. ~pplication No. 08/316,259 (Christianson) filed 30 September 1994, assigned to the assignee ofthe present invention.
1 5 Useful al-lmimlm oxide grains for applications of the present invention include fused alllrninum oxides, heat treated aluminum oxides, and ceramic alllmimlm oxides. Examples of such ceramic alllmimlrn oxides are disclosed in U.S. Patent Nos. 4,314,827 (Leitheiser et al.), 4,744,802 (Schwabel), 4,770,671 (Monroe et al.), and 4,881,951 (Wood et al.).
2 0 The average particle size of the abrasive particle for advantageous applications of the present invention is at least about 0.1 micrometers, preferably at least about 100 micrometers. A grain size of about 100 micrometers corresponds approximately to a coated abrasive grade 120 abrasive grain, according to Arnerican National Standards Institute (ANSI) Standard B74.18- 1984. The 2 5 abrasive grain can be oriented, or it can be applied to the backing withoutorientation, depending upon thle desired end use of the coated abrasive backing.The abrasive particles can be embedded into the make coat precursor by any conventional technique such as electrostatic coating, drop coating, or magnetic coating. During electrostatic coatimg, eleckostatic charges are applied to the 3 0 abrasive particles and this propels the abrasive particles upward. Electrostatic coating tends to orient the abrasive particle, which generally leads to better CA 02227~18 1998-01-21 WO 97/05990 PCT~US96/12791 abrading performance. In drop coating, the abrasive particles are forced from a feed station and fall into the binder precursor by gravity. It is also wit_in the scope of this invention to propel the abrasive particles upward by a mech~niç~l force into the binder precursor. Magnetic coating involves using m~neti~ forces to coat theabrasive particles.
If the abrasive particles are applied by eleckostatic coating, then it is erell~d that the backing be placed on a drum. This drum can be the original support structure or a different drum. The drum serves as a ground for the electrostatic coating process. The proper amount of abrasive particles is then placed on a plate underneath the drum. Next, the drum is rotated and the electrostatic field is turned on. As the drum rotates, the abrasive particles are embedded into the make coat. The drum is rotated until the desired arnount of abrasive particles is coated. The resulting construction is exposed to conditions sufficient to solidify the make coat.
Alternately, a charged plate can be used as the ground for the electrostatic process instead of the drum.
Size Coat A size coat, or third a&esive layer, may be applied over the abrasive particles and the make coat such as by roll coating or spray coating. The plc;r..led 2 0 size coat is a resole phenolic resin filled with a silane treated calcium met~iliç~t~.
After the size coat is applied, the size coat is solidified, typically upon exposure to an energy source. These energy sources include both thermal and radiation energy.

Su~cl~ Coat 2 5 In some instances it may be preferred to apply a supersize coat, or fourth adhesive layer, over the size coat. The optional supersize coat can preferably include a grinding aid, to çnh~nce the abrading characteristics of the coated abrasive. Examples of grinding aids include potassiurn tetrafluoroborate, cryolite, ammonium cryolite, or sulfur. One would not typically use more of a grinding aid3 0 than needed for desired results. The supersize coat may comprise a binder and a grin~ling aid.

The abrasive material can also be applied using a prefolmed abrasive coated l~min~te. This l~min~te consists of a substrate of material coated with abrasive grains. The substrate of m~teri~l can be a piece of cloth, polymeric film, vulcanized fiber paper, and the like. The l~min~t~ can be applied to the outer 5 surface of the b~cking of the present invention using; any of the a&esives discussed above; thermobonding; a ~l~a~ul~ sensitive adhesive; or mechar~ical fastening means, such as a hook and loop means, such as disclosed, for example, in U.S. Patent No. 4,609,58 l (Ott). This could include a method of att~çhment by which the l~min~te is applied to a liquid loop of bac~ing binder and }einforcing10 fiber such that the Iz~nnin~te is att~hPd by curing or solidifying the liquid backing loop. This embodiment of the coated abrasive article of the present invention isadvantageous at least because of the potential for removing the l~min~t~ once the abrasive material is exhausted and replacing it with another such l~nnin:~te In this way the backing of the present invention can be recycled and reused.
The following non-limiting exarnples will further illustrate the invention.
All parts, percentages, ratios, etc.~ in the exarnples are by weight unless otherwise indicated.
EXAMPLES
The following 11eci~n,ltions are used throughout the exarnples.
DW: deionized water;
SCA: silane coupling agent, commercially available from OSi Specialties (Danbury, CT)Iunder the trade deci~n~tion "A-l lO0";
ASC: arnorphous silica clay, commercially available from DeGussa 2 5 GMBH (Germany) under the trade clesign~tion "Peerless #4";
RPR: resole phenolic resin, cont~ininp between 0.75 to 1.4% free formaldehyde and 6 to 8% free phenol, percent solids about 78%
with the rem~in~1er being water, pH about 8.5, and viscosity between about 2400 and 2800 centipoise;
3 0 ASF: arnorphous silica filler, commercially available from DeGussa GMBH (Germany) under the trade designation "Aerosil R-972";

W O 97/05990 PCT~US96/12791 HLR: latex resin, commercially available from B.F. Goodrich (Cleveland, OH) under the trade designation "Hycar 1581";
SWAl: wetting agent, commercially available from Akzo Chemie America (Chicago, IL) under the trade ~leeign~tion "Interwet 33";
SWA2: wetting agent, commercially available from Union Carbide Corp.
(Danbury, CT) under the trade ~leeign~tion "Silwet L-7604";
ERH: epoxy resin, commercially available from Shell Chemical Co.
(Houston, TX) under the trade ~lçeign~tion "Epon 828";
POPDA: polyoxypropylene~ mine commercially available from H-lntem~n Corp. (Salt Lake City, UT) under the trade clesign~tion "Jçff~mine D-230";
UR1: a polyether based polyurethane resin commercially available from Uniroyal Chemical Corp. (Middlebury, CT) under the trade ~leei~n~tion "Adiprene L-167";
DMTA: di(methylthio)toluenef~i~mine commercially available from Albemarle Corporation (Baton Rouge, LA) under the trade deci~n~tion "Ethacure 300";
TPGA: ~ o~yleneglycoldiacrylate commercially available from Sartomer (West Chester, PA) under the trade deei~n~tion "SR-306";
2 0 PH2: 2-benzyl-2-N,N-dimethylamino-1 -(4-morpholinophenyl)-1-butanone, commercially available from Ciba Geigy Corp.
(Hawthorn, NY) under the trade d~sign~tion "Irgacure 369";
CMSK: calcium met~eilic~lte, commercially available from NYCO
(Willsboro, NY) under the trade cl~signzltion "400 Woll~etokl-p";
IO: iron oxide pigment, commercially available from Harcros Pigments, Inc. (Fairview Heights, IL) under the trade designation "Kroma Red Iron Oxide";
GBF: glass bubbles, commercially available from Minnesota Mining and M:~nllf~ctl-rin~: Co. (St. Paul, MN) under the trade design~tion "Scotchlite H50/10,000 EPX".

-WO 97/05990 PCT~US96/12791 Example 1 An endless spliceless polyester/cotton backing substrate available from Advanced Belt Technology (Middletown, CT) under the ~lesi~tion "WT-3", was provided. The weave was a 2 cotton over 1 polyester weave, with cotton in the 5 warp (machine) direction and polyester in the weft (fill) direction. The polyester was about 11 threads/cm, and the cotton was about 45 threads/cm. The polyester was in belt circumference and the cotton was in the cross direction. The length of thesplicelessbackingwas335.3 cm(132inches)andthewidthwas30.5cm(12 inches).
The spliceless backing loop substrate was rinsed in tap water and placed over an all-minl~m hub which had a circumference of 335.3 cm, a width of 38.1 cm, and a wall thickness of 0.64 cm. The hub was installed on a 7.6 cm mandrel that rotated by a DC motor and was capable of rotating from 1 to 45 revolutions per minute (rpms).
A backing S~ L was applied to the spliceless backing once it was on the hub. A layer of resin, having lhe following formulation, was coated onto the spliceless backing loop substr~lte: 25 parts DW, 0.5 part SCA, 14 parts ASC, 21.5 parts RPR, 2.5 parts ASF, 36 parts HLR, 0.25 part SWAl, and 0.25 part SWA2.
The viscosity of this ~lu~ l resin was 310 cps when measured at 34~ C with a 2 0 Brookfield Viscometer, spindle 2, at 60 rpm. The wet weight of the ~a~u~
coating was approximately 0.0325 gram per square cm (0.21 gram per inch) and soaked approximately half the thickness of the backing loop. After coating, the drum was rotated at 3 rpm and the saturant coating was dried and partially curedusing infrared heaters.
2 5 An epoxy resin coating, referred to as a 'pre-size", having the following formulation, was coated onto t~he saturated spliceless backing: 73 parts ERH, 24.35 parts POPDA, 2.4 parts ASF, and 0.25 part SWA2. The wet weight of this epoxy coating was approximately 0.009 gram per square cm (0.06 grarn per square inch).After coating, the drum was rotated at 3 rpm and the coating was partially cured3 0 using the infrared heaters as above.

CA 02227~18 1998-01-21 W 097/05990 PCTrUS96/12791 A urethane resin fonn~ tion, known as the "winding" resin, having the following formulation, was coated onto the cured pre-size coating to form a "base layer": 50 parts URl, 23 parts DMTA, 26 parts TPGA, 0.5 part PH2, and 0.5 part SWA2. The wet weight of this coating was ~ o~i"~ately 0.0325 gram per square cm (0.21 gram per square inch). After coating, a doctor blade was used to smooththe winding resin. The smoothed resin then cured for 60 seconds with a (600 watt/inch) "V" bulb from Fusion Systems.
A second layer of winding resin was coated on top of the cured base layer, by the methods described above. After smoothing, 800 denier "KEVLAR 49" fiber 1 0 available from Synthetic Thread Co. Inc., Bethlehem, PA, was wound onto andinto the smoothed resin at about 16.5 threads per cm (42 threads per inch) of belt width. The fibers were essentially engulfed by the resin. The "KEVLAR" fibers strengthen the final backing and minimi7:~? stretch. The strands were first run through a tensioner and then wound through a comb, two at a time. The 1 5 ,~;nfolcillg fibrous strands were wrapped over the spliceless backing loop ~ub~lla~
by means of a yarn guide system with a level winder that moved across the face of the hub at a rate of 10 cm per minute. During this process, the hub rotated at 45 rpm. After Wl~illg, the resin and fibers were smoothed with a doctor blade, and cured for 60 seconds with the same "V" lamp.
2 0 Another layer of winding resin was coated at the same resin weight directly ontop of the previously cured resin. This was then cured for 60 seconds with thesame "V" bulb.
The fiber reinforced backing structure was removed from the hub and turned inside out, i.e. everted, so that the reinforcing fibers were located on the 2 5 inside of the loop.

Exam~le 2 Example 2 was prepared in the same manner as Example 1, except that after the layers of winding resin were coated and cured, approximately 0.12-0.25 mm (5-3 0 10 mils) of cured resin was ground off with a Doall D- 10 grinder (The Doall Company, Des Plaines, IL) using 180 micron Imperial Microfini~hing Film (from W O 97/05990 PCT~US96/12791 Mirmesota Mining and ~slnllf~chlring Co.). This act of grinding the back aided in smoothing the backing further and providing an even caliper.

Example 3 Example 3 was ~cpal~d in the same manner as Exarnple 1, except that after applying and smoothing the second layer of winding resin, a third layer of winding resin was coated and smoothed. A second layer of fiber was wound into and onto the smoothed resin. The resin was cured, and a fourth layer of resin was coated and cured. The resulting belt was everted.

Example 4 Example 4 was prepared in the sarne manner as Example 3, except that after the final cure, the belt was removed from the hub, and slit to 7.62 cm (3 inches).
These slit strips were moved to a mandrel (reinforcing fibers out), and approximately 0.12-0.25 mm (5-10 mils) of cured resin was ground off with a Doall D-10 grinder using 180 micron Imperial Microfini~hin~ Film (from Minnesota M[ining and Manufacturing Co.). This act of grintling the back aided in smoothing the backing further and providing an even caliper.
The following designations are used throughout the examples, particularly 2 0 for the making of the abrasive agglomerates.

SAG: cubic boron nitride grain, 140/170 mesh, ERH: epoxy resin, commercially available from Shell Chemical Co.
(Houston, TX) under the trade designation "Epon 828";
2 5 DW: deionized water;
EGME: ethylene glycol monobutyl ether, also known as polysolve, commercially available from Olin Co,l,~,y (Stamford, CT);
PS100: aromatic solvent, commercially available from Exxon Chemical Co.
(Houston, TX) under the trade ~esi~n~tions "WC-100";
3 0 EPH: epoxy hardener, cornmercially available from Henkel Corporation (Minneapolis, MN) under the trade ~leci~n~1ion "Versamid 125";

CA 02227~18 1998-01-21 GPM: glass powder, SiO2 51.5%, B2~2 27.0%, A1203 8.7%, MgO 7.5%, ZnO 2.0%, CaO 1.1%, Na2O 1.0%, K2O 1.0%, Li2O 0.5%, ground to finer than 325 mesh.

Example Example S was a coated abrasive belt made using the backing of F~mple 1 which had been slit to 7.6 cm (3 inches).
The fiber reinforced backing structure, Example I, was turned inside out, i.e., everted, so that the reinforcing fibers were on the inside, and placed under 1 0 tension on a pair of idler rolls with one roll drivable by motor to rotate the b~ n~
All resin coatings were on the polyester/cotton side of the backing.
A saturant resin, having the following formulation, was roll coated on the exposed side of spliceless backing substrate opposite the fiber reinforcing layer:
31.6 parts DW, 0.4 part SCA, 13.3 parts ASC, 20 parts RPR, 1.8 parts ASF, 32.4 parts HLR, 0.25 part SWAl, and 0.25 part SWA2. The wet weight ofthis ~Lu~
coating was appro2~im~tely 0.019 grams per square cm (0.12 gram per square inch).
The saturated backing was placed on a round hub and dried in an oven for 30 minl-tes at 90~C.
An epoxy pre-size resin, having the following formulation, was knife 2 0 coated onto the dried backing: 73 parts ERH, 24.35 parts POPDA, 2.4 parts ASF, and 0.25 part SWA2. The wet weight of this size coating was approximately 0.011 grams per square cm (0.07 gram per square inch). The coated backing was placed on a round hub and cured in an oven for 30 mim~te~ at 90~C.
A phenolic make resin, having the following formulation, was knife coated 2 5 in a 5.7 cm (2.25 inch) wide path on the 7.6 cm (3 inch) wide backing: 34.29 parts RPR, 12.46 parts DW, 51.85 parts CMSK, 0.75 part ASF, 0.19 part ASC, 0.23 part SWAl, and 0.23 part SWA2. The knife setting (gap) was set at 0.3 mm (0.013 inch).
Vitrified agglomerates were prepared according to the method described 3 0 below. A glass binder, GPM, was form~ ted so that its coefficient of th.orm~l CA 02227~18 1998-01-21 W O 97/05990 PCT~US96/12791 expansion was approximately the sarne as the coefficient of thermal expansion of the superabrasive grains used in the exarnples (3.5 x 10-6 / ~C).
Vitrified agglomerates were formed by mixing the following formulation to forrn a slurry: 47.2 parts SAG, 17.7 parts GP, 6.8 parts ERH, 3 parts ERH, 3 parts PS100, and 22.3 parts 85/15 EGME/DW. The slurry was knife coated into a silicone mold with holes approximate 1016 micrometers deep, long, and wide (0.040 inch). The slurry was dried and cured in the mold at 90~C for 30 minllt~s The resulting cubes were removed from the mold. To prevent the agglomerates from sticking together during the firing process, the dried agglomerates were placed in a bed of 220/230 mesh SAG in an alumina sagger. The sagger was placed in a small furnace that was open to the air. The furnace temperature was increased from 25~C to 900~C over a four hour period, after which it was held at 900~C for 3 hours, and then turned off and allowed tocool to room temperature overnight. The fired, vitrified agglomerates were screened through a 16 mesh screen to separate them from each other and also remove any fine SAG.
The vitrified agglomerates, prepared above, were drop coated at a weight of 0.093 gram per square cm (0.60 gram per square inch) onto and into the phenolic make resin described above. The belts were placed on a nearly 2 0 circular hub and in an oven at 90~C for 90 minlltes and at 1 55~C for 30 minutes.
A phenolic size resin, having the following formulation, was roll coated onto the agglomerates: 30.06 parts RPR, 28.48 parts DW, 0.37 part SCA, 37.34 parts CMSK, 0.19 part IO, 1.21 parts GBF, 0.23 part SWA1, and 0.23 part 2 5 SWA2. The wet weight of the size coat was approximately 0.033 grams per square cm (0.21 gram per square inch). The belts were placed in an oven at 90~C for 90 minntes7 105~C for 10 hours, and at 130~C for 3 hours.

WO 97/05990 PCT~US96/12791 .
Example 6 Example 6 was prepared in the same manner as Example 5, except the backing used was that of F~mple4.
The invention has been described with reference to various specific and 5 ~l~fclled embodiments and techniques. It should be understood, however, that many variations and modifications can be made while rem~inin~ within the spirit and scope of the invention.

Claims (14)

1. A method of making a flexible coated abrasive belt comprising the steps of:
(a) mounting an endless, spliceless backing loop substrate having an exposed front surface and a back surface tautly on a peripheral surface of a temporary support structure;
(b) applying a continuous fibrous reinforcing material onto said front surface in a plurality of revolutions;
(c) applying a coating of a first binder precursor onto said front surface;
(d) exposing said coating to conditions effective to solidify said first binder precursor and bond said fibrous reinforcing material to said front surface to form an endless spliceless reinforced backing; and (e) applying an abrasive coating comprising abrasive particles and adhesive over said back surface or said front surface of said endless spliceless reinforced backing.
2. The method of claim 1, wherein step (c) is conducted before step (b).
3. The method of claim 1, wherein step (e) is conducted before step (a).
4. A method of making a flexible coated abrasive belt comprising the steps of:
(a) mounting an endless, spliceless backing loop substrate having an exposed front surface and a back surface tautly on a peripheral surface of a temporary support structure;
(b) at least partially saturating said substrate with a saturant resin precursor;
(c) at least partially curing said saturant resin precursor;
(d) applying a coating of a pre-size precursor onto said front surface;
(e) at least partially curing said pre-size precursor;
(f) applying a continuous fibrous reinforcing material onto said front surface in a plurality of revolutions;
(g) applying a coating of a first binder precursor onto said front surface;
(h) exposing said coating to conditions effective to solidify said first binder precursor and bond said fibrous reinforcing material to said front surface to form an endless spliceless reinforced backing; and (i) applying an abrasive coating comprising abrasive particles and adhesive over said back surface or said front surface of said endless spliceless reinforced backing.
5. A method of making a flexible coated abrasive belt comprising the steps of:
(a) mounting an endless, spliceless backing loop substrate having an exposed front surface and back surface tautly on a peripheral surface of a temporary support structure;
(b) at least partially saturating said substrate with a saturant resin precursor;
(c) at least partially curing said saturant resin precursor;
(d) applying a coating of a pre-size precursor onto said front surface;
(e) at least partially curing said pre-size precursor;
(f) applying a fibrous reinforcing layer comprising continuous fibrous reinforcing material and binder material onto said front surface in a plurality of revolutions;
(g) applying an abrasive coating comprising abrasive particles and adhesive over said back surface or said front surface of said endless spliceless reinforced backing.
6. The method of any one of claims 1-5, wherein said fibrous reinforcing material is metallic.
7. The method of any one of claims 1-6, wherein said continuous fibrous reinforcing material is a strand.
8. The method of claim 7, wherein said fibrous reinforcing material is applied by helically winding said fibrous strand onto said front surface.
9. The method of claim 8, wherein said fibrous reinforcing strand is wound with a strand spacing of about 2 to 50 strands per cm of lateral width of said front surface.
10. The method of claim 8, wherein said helically wound strand substantiallycovers the entire lateral width of said front surface.
11. The method of any one of claims 1-6, wherein said endless spliceless backing loop substrate is selected from the group consisting of woven cloth, knitted cloth, paper, nonwoven mat, vulcanized fiber sheet, primed and unprimed polymeric film, treated versions thereof, and combinations thereof.
12. The method of any one of claims 1-6, wherein said endless spliceless backing loop is selected from the group consisting of cotton, polyester, and combinations thereof.
13. The method of any one of claims 1-6, wherein said temporary support structure is a cylinder.
14. The method of any one of claims 1-5, wherein said continuous fibrous reinforcing material is selected from the group consisting of glass, carbon, ceramic, wool, silk, cotton, cellulose, polyvinyl alcohol, polyamide, polyester,rayon, acrylic, polypropylene, aramid, ultrahigh molecular weight polyethylenes,and combinations thereof.
CA002227518A 1995-08-10 1996-08-01 Method for making a spliceless coated abrasive belt Abandoned CA2227518A1 (en)

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US08/513,325 US5578096A (en) 1995-08-10 1995-08-10 Method for making a spliceless coated abrasive belt and the product thereof
US08/513,325 1995-08-10
PCT/US1996/012791 WO1997005990A1 (en) 1995-08-10 1996-08-01 Method for making a spliceless coated abrasive belt

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Families Citing this family (90)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE176883T1 (en) * 1991-12-20 1999-03-15 Minnesota Mining & Mfg COVERED ABRASIVE BELT WITH ENDLESS, BAND-FREE BACKING AND MANUFACTURING METHOD
US5681612A (en) * 1993-06-17 1997-10-28 Minnesota Mining And Manufacturing Company Coated abrasives and methods of preparation
US5578096A (en) * 1995-08-10 1996-11-26 Minnesota Mining And Manufacturing Company Method for making a spliceless coated abrasive belt and the product thereof
FR2753766B1 (en) * 1996-09-20 1998-11-27 RIBBED BELT, ITS MANUFACTURING PROCESS AND TRANSMISSION DEVICE INCLUDING IT
JP3634952B2 (en) * 1997-11-18 2005-03-30 株式会社金陽社 Manufacturing method of transfer belt for electronic equipment
US6354929B1 (en) 1998-02-19 2002-03-12 3M Innovative Properties Company Abrasive article and method of grinding glass
US6465076B2 (en) 1998-09-15 2002-10-15 3M Innovative Properties Company Abrasive article with seamless backing
US6672952B1 (en) 1998-12-23 2004-01-06 3M Innovative Properties Company Tearable abrasive article
US6179887B1 (en) 1999-02-17 2001-01-30 3M Innovative Properties Company Method for making an abrasive article and abrasive articles thereof
US6458018B1 (en) 1999-04-23 2002-10-01 3M Innovative Properties Company Abrasive article suitable for abrading glass and glass ceramic workpieces
US6164702A (en) * 1999-06-07 2000-12-26 Adc Acquisition Company Reinforced thermoplastic pipe couping
US6919122B2 (en) 1999-07-08 2005-07-19 Saint-Gobain Performance Plastics Corporation Flexible composites with integral flights for use in high-temperature food processing equipment and methods for producing the same
US6406363B1 (en) * 1999-08-31 2002-06-18 Lam Research Corporation Unsupported chemical mechanical polishing belt
KR100564558B1 (en) * 1999-10-11 2006-03-28 삼성전자주식회사 Polishing pad using for polishing wafer surface
US6835447B2 (en) * 1999-12-15 2004-12-28 Toray Industries, Inc. Rubber reinforcing cord and fiber reinforced rubber material
US6500375B1 (en) * 2000-03-06 2002-12-31 Lexmark International Inc. Fabrication of seamless tube
US7111882B2 (en) * 2002-03-08 2006-09-26 N. V. Bekaert S.A. Reinforced impact beam with woven fabric
EP1342623A1 (en) * 2002-03-08 2003-09-10 N.V. Bekaert S.A. Reinforced impact beam
US6979713B2 (en) * 2002-11-25 2005-12-27 3M Innovative Properties Company Curable compositions and abrasive articles therefrom
US7169199B2 (en) * 2002-11-25 2007-01-30 3M Innovative Properties Company Curable emulsions and abrasive articles therefrom
US7549938B2 (en) * 2003-01-07 2009-06-23 Forbo Financial Services Ag Treadmill belt
US6951504B2 (en) * 2003-03-20 2005-10-04 3M Innovative Properties Company Abrasive article with agglomerates and method of use
WO2004101225A1 (en) * 2003-05-09 2004-11-25 Diamond Innovations, Inc. Abrasive particles having coatings with tortuous surface topography
AU2005202973A1 (en) * 2004-07-06 2006-02-02 Stephen Arthur Dickins Improvements in or Relating to Reinforced Means
US7371718B2 (en) * 2005-04-22 2008-05-13 The Dial Corporation Liquid fabric softener
US20060265967A1 (en) * 2005-05-24 2006-11-30 3M Innovative Properties Company Abrasive articles and methods of making and using the same
US20060265966A1 (en) * 2005-05-24 2006-11-30 Rostal William J Abrasive articles and methods of making and using the same
JP2006334696A (en) * 2005-05-31 2006-12-14 Sankyo Rikagaku Co Ltd Polishing belt
EP1795303B1 (en) * 2005-12-07 2010-11-17 sia Abrasives Industries AG Abrasive tool
US20070193028A1 (en) * 2006-02-17 2007-08-23 Luc Brandt Method for winding a strand of material around a substrate and products formed thereby
US20080125263A1 (en) * 2006-11-03 2008-05-29 Donald Ray Belik Spliceless baler belt
US20080105517A1 (en) * 2006-11-08 2008-05-08 Donald Ray Belik Spliceless, corded baler belt
US7931554B2 (en) * 2006-12-26 2011-04-26 Tri Corp. Endless belt
CA2696428C (en) * 2007-08-03 2015-11-24 Saint-Gobain Abrasives, Inc. Abrasive article with adhesion promoting layer
FR2924041B1 (en) * 2007-11-26 2010-04-30 Arjowiggins Licensing Sas PROCESS FOR PRODUCING A REINFORCED APPLIED ABRASIVE PRODUCT AND PRODUCT OBTAINED
US20090227188A1 (en) * 2008-03-07 2009-09-10 Ross Karl A Vacuum Sander Having a Porous Pad
US8157685B2 (en) * 2009-04-01 2012-04-17 Apache Hose & Belting Co., Inc. Endless belt with binder for carcass stability
FR2954723B1 (en) * 2009-12-29 2012-04-20 Saint Gobain Abrasives Inc ABRASIVE ARTICLE COMPRISING A HOLLOW SPACE BETWEEN ITS FRONT AND REAR FACES AND METHOD OF MANUFACTURE
US8551577B2 (en) * 2010-05-25 2013-10-08 3M Innovative Properties Company Layered particle electrostatic deposition process for making a coated abrasive article
EP2576142A4 (en) * 2010-05-28 2017-09-20 Saint-Gobain Abrasives, Inc. Non-abrasive back coat for coated abrasives
PT2588275T (en) * 2010-07-02 2018-03-13 3M Innovative Properties Co Coated abrasive articles
DE102010036554A1 (en) * 2010-07-21 2012-01-26 Bamberger Kaliko Gmbh Composite material for further processing into flat abrasive products and process for its production
CN103189163B (en) * 2010-11-18 2016-06-08 3M创新有限公司 Convolution emery wheel and manufacture method
CN103370174B (en) 2010-12-31 2017-03-29 圣戈本陶瓷及塑料股份有限公司 The forming method of the abrasive grains with given shape and such particle
DE202011001416U1 (en) 2011-01-12 2011-03-24 Lohmann Gmbh & Co. Kg Heat-activated, fiber-reinforced structural adhesive
DE102011008430A1 (en) 2011-01-12 2012-07-12 Lohmann Gmbh & Co Kg Heat-activable, fiber-reinforced structural adhesive, useful as a splicing band for abrasive belts, comprises a carrier film, a fixing adhesive layer applied with reinforcing fiber, and a heat-activatable adhesive layer
US8840694B2 (en) 2011-06-30 2014-09-23 Saint-Gobain Ceramics & Plastics, Inc. Liquid phase sintered silicon carbide abrasive particles
WO2013003830A2 (en) 2011-06-30 2013-01-03 Saint-Gobain Ceramics & Plastics, Inc. Abrasive articles including abrasive particles of silicon nitride
JP5802336B2 (en) 2011-09-26 2015-10-28 サン−ゴバン セラミックス アンド プラスティクス,インコーポレイティド Abrasive product comprising abrasive particle material, abrasive cloth paper using the abrasive particle material, and forming method
KR101681526B1 (en) 2011-12-30 2016-12-01 생-고뱅 세라믹스 앤드 플라스틱스, 인코포레이티드 Composite shaped abrasive particles and method of forming same
JP6033886B2 (en) 2011-12-30 2016-11-30 サン−ゴバン セラミックス アンド プラスティクス,インコーポレイティド Shaped abrasive particles and method for forming the same
CA2862453A1 (en) 2011-12-30 2013-07-04 Saint-Gobain Ceramics & Plastics, Inc. Forming shaped abrasive particles
BR112014017050B1 (en) 2012-01-10 2021-05-11 Saint-Gobain Ceramics & Plastics, Inc. molded abrasive particle
US8840696B2 (en) 2012-01-10 2014-09-23 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
WO2013149209A1 (en) 2012-03-30 2013-10-03 Saint-Gobain Abrasives, Inc. Abrasive products having fibrillated fibers
US9200187B2 (en) 2012-05-23 2015-12-01 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
EP2866977B8 (en) 2012-06-29 2023-01-18 Saint-Gobain Ceramics & Plastics, Inc. Abrasive particles having particular shapes and methods of forming such particles
EP2906392A4 (en) 2012-10-15 2016-07-13 Saint Gobain Abrasives Inc Abrasive particles having particular shapes and methods of forming such particles
EP2938459B1 (en) 2012-12-31 2021-06-16 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
EP2978566A4 (en) 2013-03-29 2017-01-25 Saint-Gobain Abrasives, Inc. Abrasive particles having particular shapes and methods of forming such particles
TW201502263A (en) 2013-06-28 2015-01-16 Saint Gobain Ceramics Abrasive article including shaped abrasive particles
AU2014324453B2 (en) 2013-09-30 2017-08-03 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and methods of forming same
DE102013224549A1 (en) 2013-11-29 2015-06-03 Neenah Gessner Gmbh Abrasive carrier, abrasive article comprising the abrasive carrier and its manufacturing process
JP6290428B2 (en) 2013-12-31 2018-03-07 サンーゴバン アブレイシブズ,インコーポレイティド Abrasive articles containing shaped abrasive particles
US9771507B2 (en) 2014-01-31 2017-09-26 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle including dopant material and method of forming same
CN111331524B (en) 2014-04-14 2022-04-29 圣戈本陶瓷及塑料股份有限公司 Abrasive article including shaped abrasive particles
KR101884178B1 (en) 2014-04-14 2018-08-02 생-고뱅 세라믹스 앤드 플라스틱스, 인코포레이티드 Abrasive article including shaped abrasive particles
DE102014006822B4 (en) * 2014-05-08 2016-03-03 Neenah Gessner Gmbh Abrasive carrier and abrasive carrier having at least two layers of a carrier material and abrasive articles made therefrom
WO2015184355A1 (en) 2014-05-30 2015-12-03 Saint-Gobain Abrasives, Inc. Method of using an abrasive article including shaped abrasive particles
US9707529B2 (en) 2014-12-23 2017-07-18 Saint-Gobain Ceramics & Plastics, Inc. Composite shaped abrasive particles and method of forming same
US9914864B2 (en) 2014-12-23 2018-03-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particles and method of forming same
US9676981B2 (en) 2014-12-24 2017-06-13 Saint-Gobain Ceramics & Plastics, Inc. Shaped abrasive particle fractions and method of forming same
CN107636109A (en) 2015-03-31 2018-01-26 圣戈班磨料磨具有限公司 Fixed abrasive articles and its forming method
TWI634200B (en) 2015-03-31 2018-09-01 聖高拜磨料有限公司 Fixed abrasive articles and methods of forming same
PL3307483T3 (en) 2015-06-11 2020-11-16 Saint-Gobain Ceramics&Plastics, Inc. Abrasive article including shaped abrasive particles
EP3455321B1 (en) 2016-05-10 2022-04-20 Saint-Gobain Ceramics&Plastics, Inc. Methods of forming abrasive particles
WO2018063902A1 (en) 2016-09-27 2018-04-05 3M Innovative Properties Company Open coat abrasive article and method of abrading
WO2018064642A1 (en) 2016-09-29 2018-04-05 Saint-Gobain Abrasives, Inc. Fixed abrasive articles and methods of forming same
WO2018102166A1 (en) 2016-11-29 2018-06-07 Saint-Gobain Performance Plastics Corporation Composite belt profile
CN106695588B (en) * 2016-11-30 2019-03-12 淄博理研泰山涂附磨具有限公司 A kind of preparation method of magnetism tray pad
CN108217385B (en) 2016-12-12 2021-03-12 奥的斯电梯公司 Hybrid fabric laminated belt for elevator system
US10759024B2 (en) 2017-01-31 2020-09-01 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10563105B2 (en) 2017-01-31 2020-02-18 Saint-Gobain Ceramics & Plastics, Inc. Abrasive article including shaped abrasive particles
US10865148B2 (en) 2017-06-21 2020-12-15 Saint-Gobain Ceramics & Plastics, Inc. Particulate materials and methods of forming same
DE102017126627A1 (en) * 2017-11-13 2019-05-16 Cordier Spezialpapier Gmbh abrasive
WO2020099969A1 (en) 2018-11-15 2020-05-22 3M Innovative Properties Company Coated abrasive belt and methods of making and using the same
CN113039044A (en) 2018-11-15 2021-06-25 3M创新有限公司 Coated abrasive tape and methods of making and using same
CN114867582A (en) 2019-12-27 2022-08-05 圣戈本陶瓷及塑料股份有限公司 Abrasive article and method of forming the same
KR102239369B1 (en) * 2020-08-24 2021-04-09 (주)서봉텍스 Abbrasive article and method for making the same
CN114774009A (en) * 2022-05-07 2022-07-22 程伯强 Abrasive belt butt joint adhesive tape and preparation method thereof

Family Cites Families (106)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE25587E (en) * 1964-06-02 Method and apparatus for forming fiber reinforced tubes
US289879A (en) * 1883-12-11 Thomas e
US1412309A (en) * 1918-06-04 1922-04-11 Lambert Tire & Rubber Company Method of manufacturing stretchless belting
US1676845A (en) * 1925-03-21 1928-07-10 Goodyear Tire & Rubber Belt and method of making the same
US1924355A (en) * 1931-04-16 1933-08-29 Abraham L Freedlander Belt
US2032356A (en) * 1934-02-28 1936-03-03 William J Ellis Abrasive element
US2349365A (en) * 1936-07-09 1944-05-23 Carborundum Co Flexible abrasive article
US2333035A (en) * 1937-02-06 1943-10-26 Behr Manning Corp Coated abrasive
US2209074A (en) * 1938-03-28 1940-07-23 Carborundum Co Wide abrasive belt
US2404207A (en) * 1940-06-29 1946-07-16 United Cotton Products Company Abrasive belt
US2356249A (en) * 1941-04-12 1944-08-22 Dayton Rubber Mfg Co Method of making belts
US2356866A (en) * 1941-10-06 1944-08-29 Carborundum Co Manufacture of abrasive disk materials
US2391731A (en) * 1943-05-17 1945-12-25 Minnesota Mining & Mfg Spliced abrasive belt, band, and the like
US2411724A (en) * 1943-11-12 1946-11-26 Western Electric Co Method of making tubular abrasive bodies
US2468853A (en) * 1944-09-15 1949-05-03 Carborundum Co Abrasive web material
US2590697A (en) * 1949-04-08 1952-03-25 Don S Grove Endless abrasive belt and method of manufacturing same
US2682733A (en) * 1950-08-16 1954-07-06 Bay State Abrasive Products Co Flexible abrasive band
US2712987A (en) * 1951-10-09 1955-07-12 Hartford Special Machinery Co Abrading belt and method of making it
US2704735A (en) * 1951-11-05 1955-03-22 Columbus Coated Fabrics Corp Method and apparatus for casting vinyl film continuously
US2785442A (en) * 1952-01-04 1957-03-19 H D Boggs Company Ltd Method of making a reinforced hollow cylindrical article
NL88412C (en) * 1952-12-23
US2743559A (en) * 1953-04-10 1956-05-01 Bay State Abrasive Products Co Abrasive bands
US2999780A (en) * 1953-11-13 1961-09-12 H D Boggs Company Ltd Method of casting tubular articles
US2995176A (en) * 1956-11-28 1961-08-08 Dayco Corp V-belt construction
US3030743A (en) * 1958-08-06 1962-04-24 Minnesota Mining & Mfg Reinforced rotative abrasive structures
US2983637A (en) * 1958-12-23 1961-05-09 Russell Mfg Co Gear belt
GB900867A (en) * 1959-07-27 1962-07-11 George Conrad Riegger Sandpaper
US3276852A (en) * 1962-11-20 1966-10-04 Jerome H Lemelson Filament-reinforced composite abrasive articles
US3333372A (en) * 1964-12-03 1967-08-01 Pres Ou Abrasives Inc Abrasive belt
JPS49319B1 (en) * 1967-10-25 1974-01-07
US3561938A (en) * 1968-02-05 1971-02-09 Merit Products Inc Abrasive disk
US3607502A (en) * 1969-02-27 1971-09-21 Owens Corning Fiberglass Corp Industrial belt construction and method of manufacturing same
US3562968A (en) * 1969-03-12 1971-02-16 Minnesota Mining & Mfg Surface treating tool
US3577872A (en) * 1969-06-02 1971-05-11 Ppg Industries Inc Method and apparatus for coating textile material
FR2095185A2 (en) * 1970-07-13 1972-02-11 Norton Co Abrasive sheet
SE338933B (en) * 1970-01-20 1971-09-20 Fab Ab Eka
US4018574A (en) * 1970-12-16 1977-04-19 Norton Compay Process for the manufacture of endless coated abrasive articles
US4163647A (en) * 1971-06-23 1979-08-07 Norton Company Method for producing coated abrasives
GB1375571A (en) * 1971-07-27 1974-11-27
IT976997B (en) * 1972-04-15 1974-09-10 Hitachi Shipbuilding Eng Co IMPROVEMENT IN PROCEDURES AND DEVICES FOR THE MANUFACTURE OF TUBULAR ELEMENTS IN SYNTHETIC MATERIAL WITH INTERNAL REINFORCEMENT IN GLASS FIBER
CA1031967A (en) * 1973-11-07 1978-05-30 Jarvis M. Mcgarvey Endless abrasive belt, and laminated patch splice therefor
GB1445520A (en) * 1974-03-01 1976-08-11 Sankyo Rikagaku Co Tubular abrasive member
GB1475986A (en) * 1974-05-30 1977-06-10 Siaco Ltd Belts
US4049767A (en) * 1974-10-04 1977-09-20 Vaidya Deepak V Rotational molding process for forming a closed hollow toroidal article
DE2657881A1 (en) * 1976-12-21 1978-06-22 Sia Schweizer Schmirgel & Schl ABRASIVES
CA1023563A (en) * 1977-01-10 1978-01-03 James K. Cooper Method of securing an abrasive surface to an endless belt
CH610801A5 (en) * 1977-07-05 1979-05-15 Rene Crevoisier Method for manufacturing endless abrasive belts and abrasive belts obtained by this method
FR2436666A1 (en) * 1978-09-22 1980-04-18 Aerospatiale PROCESS FOR PRODUCING RESIN IMPREGNATED FABRIC CONDUITS
DE2966035D1 (en) * 1978-12-12 1983-09-08 Interface Dev Ltd Flexible abrasive member and method of making same
US4215516A (en) * 1979-04-18 1980-08-05 Sheldahl, Inc. Unidirectional tape
US4314827A (en) * 1979-06-29 1982-02-09 Minnesota Mining And Manufacturing Company Non-fused aluminum oxide-based abrasive mineral
US4253836A (en) * 1979-09-14 1981-03-03 Dayco Corporation Mobius belt and method of making the same
US4282011A (en) * 1980-05-30 1981-08-04 Dan River Incorporated Woven fabrics containing glass fibers and abrasive belts made from same
US4867760A (en) * 1980-07-31 1989-09-19 Norton Company Coated abrasive
US4588419A (en) * 1980-10-08 1986-05-13 Carborundum Abrasives Company Resin systems for high energy electron curable resin coated webs
JPS6015454B2 (en) * 1980-10-29 1985-04-19 北辰工業株式会社 Manufacturing method of thin endless belt
US4455343A (en) * 1980-12-29 1984-06-19 Ppg Industries, Inc. Aqueous treating composition for glass fiber strands used to produce mats for thermoplastics
US4373933A (en) * 1981-05-15 1983-02-15 Grazen Alfred E Method of producing precision abrasive tools
DE3219567A1 (en) * 1982-05-25 1983-12-01 SEA Schleifmittel Entwicklung Anwendung GmbH, 7530 Pforzheim ELASTIC GRINDING BODY AND METHOD FOR THE PRODUCTION THEREOF
US4554765A (en) * 1983-03-03 1985-11-26 Grimes Philip M Coated abrasive disc
US4525177A (en) * 1983-03-03 1985-06-25 Grimes Philip M Method of making coated abrasive disc
EP0142140A3 (en) * 1983-11-09 1985-06-19 Norddeutsche Schleifmittel-Industrie Christiansen &amp; Co. (GmbH &amp; Co.) Abrasive belt with a junction reinforced with a synthetic resin strip
US4653236A (en) * 1984-03-12 1987-03-31 Grimes Philip M Coated abrasive disc
CA1266569A (en) * 1984-05-09 1990-03-13 Minnesota Mining And Manufacturing Company Coated abrasive product incorporating selective mineral substitution
WO1986002306A1 (en) * 1984-10-09 1986-04-24 Minnesota Mining And Manufacturing Company Coated abrasive sheet material with improved backing
US4609581A (en) * 1985-04-15 1986-09-02 Minnesota Mining And Manufacturing Company Coated abrasive sheet material with loop attachment means
US4681558A (en) * 1985-04-18 1987-07-21 National Standard Company Reinforced polymeric component and method of manufacture
CA1254238A (en) * 1985-04-30 1989-05-16 Alvin P. Gerk Process for durable sol-gel produced alumina-based ceramics, abrasive grain and abrasive products
DE3526502A1 (en) * 1985-07-24 1987-01-29 Norddeutsche Schleifmittel Ind GRINDING BELT WITH A CONNECTING JOINT THROUGH ITS LONGITUDE
US4652275A (en) * 1985-08-07 1987-03-24 Minnesota Mining And Manufacturing Company Erodable agglomerates and abrasive products containing the same
US4652274A (en) * 1985-08-07 1987-03-24 Minnesota Mining And Manufacturing Company Coated abrasive product having radiation curable binder
US4770671A (en) * 1985-12-30 1988-09-13 Minnesota Mining And Manufacturing Company Abrasive grits formed of ceramic containing oxides of aluminum and yttrium, method of making and using the same and products made therewith
US4751138A (en) * 1986-08-11 1988-06-14 Minnesota Mining And Manufacturing Company Coated abrasive having radiation curable binder
US4799939A (en) * 1987-02-26 1989-01-24 Minnesota Mining And Manufacturing Company Erodable agglomerates and abrasive products containing the same
US4881951A (en) * 1987-05-27 1989-11-21 Minnesota Mining And Manufacturing Co. Abrasive grits formed of ceramic containing oxides of aluminum and rare earth metal, method of making and products made therewith
US4906523A (en) * 1987-09-24 1990-03-06 Minnesota Mining And Manufacturing Company Primer for surfaces containing inorganic oxide
US4894280A (en) * 1987-12-21 1990-01-16 Kimberly-Clark Corporation Flexible, tear resistant composite sheet material and a method for producing the same
DE3808426C2 (en) * 1988-03-14 1995-01-26 Hermes Schleifmittel Gmbh & Co Flexible grinding tool and process for its manufacture
DE3809513A1 (en) * 1988-03-22 1989-10-05 Olbo Textilwerke Gmbh VAPOR-PERMEABLE CONVEYOR BELT
US5082720A (en) * 1988-05-06 1992-01-21 Minnesota Mining And Manufacturing Company Melt-bondable fibers for use in nonwoven web
ES2007915A6 (en) * 1988-06-10 1989-07-01 Coteron Uriarte Jose Ramon Improvements in the manufacturing of transmission belts.
US5011508A (en) * 1988-10-14 1991-04-30 Minnesota Mining And Manufacturing Company Shelling-resistant abrasive grain, a method of making the same, and abrasive products
US4903440A (en) * 1988-11-23 1990-02-27 Minnesota Mining And Manufacturing Company Abrasive product having binder comprising an aminoplast resin
US5109638A (en) * 1989-03-13 1992-05-05 Microsurface Finishing Products, Inc. Abrasive sheet material with non-slip backing
GB8911872D0 (en) 1989-05-24 1989-07-12 Halliwell Hiram H Belt joints
JP2978180B2 (en) * 1989-07-23 1999-11-15 北村 篤識 Polishing belt and polishing machine
US5108463B1 (en) * 1989-08-21 1996-08-13 Minnesota Mining & Mfg Conductive coated abrasives
US5155945A (en) * 1990-01-29 1992-10-20 Jason, Inc. Abrasive finishing elements, tools made from such elements, and methods of making such tools
CA2036247A1 (en) * 1990-03-29 1991-09-30 Jeffrey L. Berger Nonwoven surface finishing articles reinforced with a polymer backing layer and method of making same
DE4016902A1 (en) * 1990-05-25 1991-11-28 Balatros Gmbh METHOD AND DEVICE FOR MANUFACTURING AN ENDLESS, FLAT AND FLEXIBLE TAPE FROM POWDERABLE PLASTIC
US5137542A (en) * 1990-08-08 1992-08-11 Minnesota Mining And Manufacturing Company Abrasive printed with an electrically conductive ink
US5078753A (en) * 1990-10-09 1992-01-07 Minnesota Mining And Manufacturing Company Coated abrasive containing erodable agglomerates
US5108462A (en) * 1990-12-27 1992-04-28 Exxon Research And Engineering Company Smoke reducing additive for two-cycle engine lubricant-fuel mixture
US5341609A (en) * 1992-01-28 1994-08-30 Minnesota Mining And Manufacturing Company Abrasive belts and their manufacture
US5236472A (en) * 1991-02-22 1993-08-17 Minnesota Mining And Manufacturing Company Abrasive product having a binder comprising an aminoplast binder
JPH06509519A (en) * 1991-07-30 1994-10-27 ミネソタ・マイニング・アンド・マニュファクチュアリング・カンパニー Coated abrasive tool dressed with multi-point cutting tool
JPH05208422A (en) * 1991-09-17 1993-08-20 Xerox Corp Manufacture of image forming member
US5316812A (en) * 1991-12-20 1994-05-31 Minnesota Mining And Manufacturing Company Coated abrasive backing
ATE176883T1 (en) * 1991-12-20 1999-03-15 Minnesota Mining & Mfg COVERED ABRASIVE BELT WITH ENDLESS, BAND-FREE BACKING AND MANUFACTURING METHOD
US5203884A (en) * 1992-06-04 1993-04-20 Minnesota Mining And Manufacturing Company Abrasive article having vanadium oxide incorporated therein
US5344688A (en) * 1992-08-19 1994-09-06 Minnesota Mining And Manufacturing Company Coated abrasive article and a method of making same
CA2088866C (en) * 1993-02-05 2004-07-20 Daniel W. Wuerch Non-spotting overspray masking composition
US5436063A (en) * 1993-04-15 1995-07-25 Minnesota Mining And Manufacturing Company Coated abrasive article incorporating an energy cured hot melt make coat
GB9310398D0 (en) * 1993-05-20 1993-07-07 Minnisota Mining And Manufactu Process for the manufacture of endless coated abrasive articles
AU1735295A (en) * 1994-02-22 1995-09-04 Minnesota Mining And Manufacturing Company Method for making an endless coated abrasive article and the product thereof
US5578096A (en) * 1995-08-10 1996-11-26 Minnesota Mining And Manufacturing Company Method for making a spliceless coated abrasive belt and the product thereof

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EP0843611B1 (en) 2000-12-27
CN1192712A (en) 1998-09-09
JPH11510438A (en) 1999-09-14
WO1997005990A1 (en) 1997-02-20
EP0843611A1 (en) 1998-05-27
DE69611372T2 (en) 2001-05-23
US5830248A (en) 1998-11-03
MX9800994A (en) 1998-04-30
KR19990036316A (en) 1999-05-25
US5578096A (en) 1996-11-26
BR9609906A (en) 1999-06-15
AU6718796A (en) 1997-03-05
DE69611372D1 (en) 2001-02-01

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