Abrasive particles and abrasive articles made from the abrasive particles are useful for abrading, finishing, or grinding a wide variety of materials and surfaces in the manufacturing of goods. For example, finishing of welding beads, flash, gates, and risers off castings by off-hand abrading with a handheld right-angle grinder is an important application for coated abrasive discs. There continues to be a need for improving the cost, performance and other features of the abrasive articles.
The drawings illustrate generally, by way of example, but not by way of limitation, various embodiments discussed in the present document.
Reference will now be made in detail to certain embodiments of the disclosed subject matter, examples of which are illustrated in part in the accompanying drawings. While the disclosed subject matter will be described in conjunction with the enumerated claims, it will be understood that the exemplified subject matter is not intended to limit the claims to the disclosed subject matter.
Throughout this document, values expressed in a range format should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. For example, a range of “about 0.1% to about 5%” or “about 0.1% to 5%” should be interpreted to include not just about 0.1% to about 5%, but also the individual values (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.1% to 0.5%, 1.1% to 2.2%, 3.3% to 4.4%) within the indicated range. The statement “about X to Y” has the same meaning as “about X to about Y,” unless indicated otherwise. Likewise, the statement “about X, Y, or about Z” has the same meaning as “about X, about Y, or about Z,” unless indicated otherwise.
In this document, the terms “a,” “an,” or “the” are used to include one or more than one unless the context clearly dictates otherwise. The term “or” is used to refer to a nonexclusive “or” unless otherwise indicated. The statement “at least one of A and B” has the same meaning as “A, B, or A and B.” In addition, it is to be understood that the phraseology or terminology employed herein, and not otherwise defined, is for the purpose of description only and not of limitation. Any use of section headings is intended to aid reading of the document and is not to be interpreted as limiting; information that is relevant to a section heading may occur within or outside of that particular section.
In the methods described herein, the acts can be carried out in any order without departing from the principles of the disclosure, except when a temporal or operational sequence is explicitly recited. Furthermore, specified acts can be carried out concurrently unless explicit claim language recites that they be carried out separately. For example, a claimed act of doing X and a claimed act of doing Y can be conducted simultaneously within a single operation, and the resulting process will fall within the literal scope of the claimed process.
The term “about” as used herein can allow for a degree of variability in a value or range, for example, within 10%, within 5%, or within 1% of a stated value or of a stated limit of a range, and includes the exact stated value or range.
The term “substantially” as used herein refers to a majority of, or mostly, as in at least about 50%, 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99%, 99.5%, 99.9%, 99.99%, or at least about 99.999% or more, or 100%.
As used herein “shaped abrasive particle” means an abrasive particle having a predetermined or non-random shape. One process to make a shaped abrasive particle such as a shaped ceramic abrasive particle includes shaping the precursor ceramic abrasive particle in a mold having a predetermined shape to make ceramic shaped abrasive particles. Ceramic shaped abrasive particles, formed in a mold, are one species in the genus of shaped ceramic abrasive particles. Other processes to make other species of shaped ceramic abrasive particles include extruding the precursor ceramic abrasive particle through an orifice having a predetermined shape, printing the precursor ceramic abrasive particle though an opening in a printing screen having a predetermined shape, or embossing the precursor ceramic abrasive particle into a predetermined shape or pattern. In other examples, the shaped ceramic abrasive particles can be cut from a sheet into individual particles. Examples of suitable cutting methods include mechanical cutting, laser cutting, or water jet cutting. Non-limiting examples of shaped ceramic abrasive particles include shaped abrasive particles, such as triangular plates, or elongated ceramic rods/filaments. Shaped ceramic abrasive particles are generally homogenous or substantially uniform and maintain their sintered shape without the use of a binder such as an organic or inorganic binder that bonds smaller abrasive particles into an agglomerated structure and excludes abrasive particles obtained by a crushing or comminution process that produces abrasive particles of random size and shape. In many embodiments, the shaped ceramic abrasive particles comprise a homogeneous structure of sintered alpha alumina or consist essentially of sintered alpha alumina.
The present application discloses abrasive articles that include shaped abrasive particles, non-shaped abrasive particles or a combination thereof. The abrasive articles can include one or more camouflaging layers that can be uniformly or randomly applied to the abrasive article. The one or more camouflaging or masking layers can minimize or mask any imperfections on the abrasive article in terms of particle placement or voids on the abrasive article where particles are not present, such as a splice. The camouflaging layer can be applied as a discontinuous layer to a portion of a size coat layer of the abrasive article and the discontinuous layer can have a color that is markedly different than a color of the size coat. The discontinuous colored layer can be applied as a repeating pattern on the abrasive article or randomly on the abrasive article. Such design having a discontinuous colored layer can be applicable to abrasive articles in the form of sheets, discs, belts, pads, or rolls. As described further below, such design may provide one or more possible advantages.
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In any of shaped abrasive particles 200A-200E, the edges can have the same length or different lengths. The length of any of the edges can be any suitable length. As an example, the length of the edges can be in a range of from about 0.5 μm to about 2000 μm, about 150 μm to about 200 μm, or less than, equal to, or greater than about 0.5 μm, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, 1500, 1550, 1600, 1650, 1700, 1750, 1800, 1850, 1900, 1950, or about 2000 μm. shaped abrasive particles 200A-200E can be the same size or different sizes.
Any of shaped abrasive particles 100 or 200 can include any number of shape features. The shape features can help to improve the cutting performance of any of shaped abrasive particles 100 or 200. Examples of suitable shape features include an opening, a concave surface, a convex surface, a groove, a ridge, a fractured surface, a low roundness factor, or a perimeter comprising one or more corner points having a sharp tip. Individual shaped abrasive particles can include any one or more of these features.
In addition to the materials already described, at least one magnetic material may be included within or coated to shaped abrasive particle 100 or 200. Examples of magnetic materials include iron; cobalt; nickel; various alloys of nickel and iron marketed as Permalloy in various grades; various alloys of iron, nickel and cobalt marketed as Fernico, Kovar, FerNiCo I, or FerNiCo II; various alloys of iron, aluminum, nickel, cobalt, and sometimes also copper and/or titanium marketed as Alnico in various grades; alloys of iron, silicon, and aluminum (about 85:9:6 by weight) marketed as Sendust alloy; Heusler alloys (e.g., Cu2MnSn); manganese bismuthide (also known as Bismanol); rare earth magnetizable materials such as gadolinium, dysprosium, holmium, europium oxide, alloys of neodymium, iron and boron (e.g., Nd2Fe14B), and alloys of samarium and cobalt (e.g., SmCo5); MnSb; MnOFe2O3; Y3Fe5O12; CrO2; MnAs; ferrites such as ferrite, magnetite, zinc ferrite; nickel ferrite; cobalt ferrite, magnesium ferrite, barium ferrite, and strontium ferrite; yttrium iron garnet; and combinations of the foregoing. In some embodiments, the magnetizable material is an alloy containing 8 to 12 weight percent aluminum, 15 to 26 wt % nickel, 5 to 24 wt % cobalt, up to 6 wt % copper, up to 1% titanium, wherein the balance of material to add up to 100 wt % is iron. In some other embodiments, a magnetizable coating can be deposited on an abrasive particle 100 using a vapor deposition technique such as, for example, physical vapor deposition (PVD) including magnetron sputtering.
Including these magnetizable materials can allow shaped abrasive particle 100 or 200 to be responsive a magnetic field. Any of shaped abrasive particles 100 or 200 can include the same material or include different materials.
Shaped abrasive particle 100 or 200 can be formed in many suitable manners for example, the shaped abrasive particle 100 or 200 can be made according to a multi-operation process. The process can be carried out using any material or precursor dispersion material. Briefly, for embodiments where shaped abrasive particles 100 or 200 are monolithic ceramic particles, the process can include the operations of making either a seeded or non-seeded precursor dispersion that can be converted into a corresponding (e.g., a boehmite sol-gel that can be converted to alpha alumina); filling one or more mold cavities having the desired outer shape of shaped abrasive particle 100 with a precursor dispersion; drying the precursor dispersion to form precursor shaped abrasive particle; removing the precursor shaped abrasive particle 100 from the mold cavities; calcining the precursor shaped abrasive particle 100 to form calcined, precursor shaped abrasive particle 100 or 200; and then sintering the calcined, precursor shaped abrasive particle 100 or 200 to form shaped abrasive particle 100 or 200. The process will now be described in greater detail in the context of alpha-alumina-containing shaped abrasive particle 100 or 200. In other embodiments, the mold cavities may be filled with a melamine to form melamine shaped abrasive particles.
The process can include the operation of providing either a seeded or non-seeded dispersion of a precursor that can be converted into ceramic. In examples where the precursor is seeded, the precursor can be seeded with an oxide of an iron (e.g., FeO). The precursor dispersion can include a liquid that is a volatile component. In one example, the volatile component is water. The dispersion can include a sufficient amount of liquid for the viscosity of the dispersion to be sufficiently low to allow filling mold cavities and replicating the mold surfaces, but not so much liquid as to cause subsequent removal of the liquid from the mold cavity to be prohibitively expensive. In one example, the precursor dispersion includes from 2 percent to 90 percent by weight of the particles that can be converted into ceramic, such as particles of aluminum oxide monohydrate (boehmite), and at least 10 percent by weight, or from 50 percent to 70 percent, or 50 percent to 60 percent, by weight, of the volatile component such as water. Conversely, the precursor dispersion in some embodiments contains from 30 percent to 50 percent, or 40 percent to 50 percent solids by weight.
Examples of suitable precursor dispersions include zirconium oxide sols, vanadium oxide sols, cerium oxide sols, aluminum oxide sols, and combinations thereof. Suitable aluminum oxide dispersions include, for example, boehmite dispersions and other aluminum oxide hydrates dispersions. Boehmite can be prepared by known techniques or can be obtained commercially. Examples of commercially available boehmite include products having the trade designations “DISPERAL” and “DISPAL”, both available from Sasol North America, Inc., or “HIQ-40” available from BASF Corporation. These aluminum oxide monohydrates are relatively pure; that is, they include relatively little, if any, hydrate phases other than monohydrates, and have a high surface area.
The physical properties of the resulting shaped abrasive particle 100 or 200 can generally depend upon the type of material used in the precursor dispersion. As used herein, a “gel” is a three-dimensional network of solids dispersed in a liquid.
The precursor dispersion can contain a modifying additive or precursor of a modifying additive. The modifying additive can function to enhance some desirable property of the abrasive particles or increase the effectiveness of the subsequent sintering step. Modifying additives or precursors of modifying additives can be in the form of soluble salts, such as water-soluble salts. They can include a metal-containing compound and can be a precursor of an oxide of magnesium, zinc, iron, silicon, cobalt, nickel, zirconium, hafnium, chromium, yttrium, praseodymium, samarium, ytterbium, neodymium, lanthanum, gadolinium, cerium, dysprosium, erbium, titanium, and mixtures thereof. The particular concentrations of these additives that can be present in the precursor dispersion can be varied.
The introduction of a modifying additive or precursor of a modifying additive can cause the precursor dispersion to gel. The precursor dispersion can also be induced to gel by application of heat over a period of time to reduce the liquid content in the dispersion through evaporation. The precursor dispersion can also contain a nucleating agent. Nucleating agents suitable for this disclosure can include fine particles of alpha alumina, alpha ferric oxide or its precursor, titanium oxides and titanates, chrome oxides, or any other material that will nucleate the transformation. The amount of nucleating agent, if used, should be sufficient to effect the transformation of alpha alumina.
A peptizing agent can be added to the precursor dispersion to produce a more stable hydrosol or colloidal precursor dispersion. Suitable peptizing agents are monoprotic acids or acid compounds such as acetic acid, hydrochloric acid, formic acid, and nitric acid. Multiprotic acids can also be used, but they can rapidly gel the precursor dispersion, making it difficult to handle or to introduce additional components. Some commercial sources of boehmite contain an acid titer (such as absorbed formic or nitric acid) that will assist in forming a stable precursor dispersion.
The precursor dispersion can be formed by any suitable means; for example, in the case of a sol-gel alumina precursor, it can be formed by simply mixing aluminum oxide monohydrate with water containing a peptizing agent or by forming an aluminum oxide monohydrate slurry to which the peptizing agent is added.
Defoamers or other suitable chemicals can be added to reduce the tendency to form bubbles or entrain air while mixing. Additional chemicals such as wetting agents, alcohols, or coupling agents can be added if desired.
A further operation can include providing a mold having at least one mold cavity, or a plurality of cavities formed in at least one major surface of the mold. In some examples, the mold is formed as a production tool, which can be, for example, a belt, a sheet, a continuous web, a coating roll such as a rotogravure roll, a sleeve mounted on a coating roll, or a die. In one example, the production tool can include polymeric material. Examples of suitable polymeric materials include thermoplastics such as polyesters, polycarbonates, poly(ether sulfone), poly(methyl methacrylate), polyurethanes, polyvinylchloride, polyolefin, polystyrene, polypropylene, polyethylene or combinations thereof, or thermosetting materials. In one example, the entire tooling is made from a polymeric or thermoplastic material. In another example, the surfaces of the tooling in contact with the precursor dispersion while the precursor dispersion is drying, such as the surfaces of the plurality of cavities, include polymeric or thermoplastic materials, and other portions of the tooling can be made from other materials. A suitable polymeric coating can be applied to a metal tooling to change its surface tension properties, by way of example.
A polymeric or thermoplastic production tool can be replicated off a metal master tool. The master tool can have the inverse pattern of that desired for the production tool. The master tool can be made in the same manner as the production tool. In one example, the master tool is made out of metal (e.g., nickel) and is diamond-turned. In one example, the master tool is at least partially formed using stereolithography. The polymeric sheet material can be heated along with the master tool such that the polymeric material is embossed with the master tool pattern by pressing the two together. A polymeric or thermoplastic material can also be extruded or cast onto the master tool and then pressed. The thermoplastic material is cooled to solidify and produce the production tool. If a thermoplastic production tool is utilized, then care should be taken not to generate excessive heat that can distort the thermoplastic production tool, limiting its life.
Access to cavities can be from an opening in the top surface or bottom surface of the mold. In some examples, the cavities can extend for the entire thickness of the mold. Alternatively, the cavities can extend only for a portion of the thickness of the mold. In one example, the top surface is substantially parallel to the bottom surface of the mold with the cavities having a substantially uniform depth. At least one side of the mold, the side in which the cavities are formed, can remain exposed to the surrounding atmosphere during the step in which the volatile component is removed.
The cavities have a specified three-dimensional shape to make shaped abrasive particle 100. The depth dimension is equal to the perpendicular distance from the top surface to the lowermost point on the bottom surface. The depth of a given cavity can be uniform or can vary along its length and/or width. The cavities of a given mold can be of the same shape or of different shapes.
A further operation involves filling the cavities in the mold with the precursor dispersion (e.g., by a conventional technique). In some examples, a knife roll coater or vacuum slot die coater can be used. A mold release agent can be used to aid in removing the particles from the mold if desired. Examples of mold release agents include oils such as peanut oil or mineral oil, fish oil, silicones, polytetrafluoroethylene, zinc stearate, and graphite. In general, a mold release agent such as peanut oil, in a liquid, such as water or alcohol, is applied to the surfaces of the production tooling in contact with the precursor dispersion such that from about 0.1 mg/in2 (0.6 mg/cm2) to about 3.0 mg/in2 (20 mg/cm2), or from about 0.1 mg/in2 (0.6 mg/cm2) to about 5.0 mg/in2 (30 mg/cm2), of the mold release agent is present per unit area of the mold when a mold release is desired. In some embodiments, the top surface of the mold is coated with the precursor dispersion. The precursor dispersion can be pumped onto the top surface.
In a further operation, a scraper or leveler bar can be used to force the precursor dispersion fully into the cavity of the mold. The remaining portion of the precursor dispersion that does not enter the cavity can be removed from the top surface of the mold and recycled. In some examples, a small portion of the precursor dispersion can remain on the top surface, and in other examples the top surface is substantially free of the dispersion. The pressure applied by the scraper or leveler bar can be less than 100 psi (0.6 MPa), or less than 50 psi (0.3 MPa), or even less than 10 psi (60 kPa). In some examples, no exposed surface of the precursor dispersion extends substantially beyond the top surface.
In those examples where it is desired to have the exposed surfaces of the cavities result in planar faces of the shaped abrasive particles, it can be desirable to overfill the cavities (e.g., using a micronozzle array) and slowly dry the precursor dispersion.
A further operation involves removing the volatile component to dry the dispersion. The volatile component can be removed by fast evaporation rates. In some examples, removal of the volatile component by evaporation occurs at temperatures above the boiling point of the volatile component. An upper limit to the drying temperature often depends on the material the mold is made from. For polypropylene tooling, the temperature should be less than the melting point of the plastic. In one example, for a water dispersion of from about 40 to 50 percent solids and a polypropylene mold, the drying temperatures can be from about 90° C. to about 165° C., or from about 105° C. to about 150° C., or from about 105° C. to about 120° C. Higher temperatures can lead to improved production speeds but can also lead to degradation of the polypropylene tooling, limiting its useful life as a mold.
During drying, the precursor dispersion shrinks, often causing retraction from the cavity walls. For example, if the cavities have planar walls, then the resulting shaped abrasive particle 100 can tend to have at least three concave major sides. It is presently discovered that by making the cavity walls concave (whereby the cavity volume is increased) it is possible to obtain shaped abrasive particle 100 that have at least three substantially planar major sides. The degree of concavity generally depends on the solids content of the precursor dispersion.
A further operation involves removing resultant precursor shaped abrasive particle 100 from the mold cavities. The precursor shaped abrasive particle 100 or 200 can be removed from the cavities by using the following processes alone or in combination on the mold: gravity, vibration, ultrasonic vibration, vacuum, or pressurized air to remove the particles from the mold cavities.
The precursor shaped abrasive particle 100 or 200 can be further dried outside of the mold. If the precursor dispersion is dried to the desired level in the mold, this additional drying step is not necessary. However, in some instances it can be economical to employ this additional drying step to minimize the time that the precursor dispersion resides in the mold. The precursor shaped abrasive particle 100 or 200 will be dried from 10 to 480 minutes, or from 120 to 400 minutes, at a temperature from 50° C. to 160° C., or 120° C. to 150° C.
A further operation involves calcining the precursor shaped abrasive particle 100 or 200. During calcining, essentially all the volatile material is removed, and the various components that were present in the precursor dispersion are transformed into metal oxides. The precursor shaped abrasive particle 100 or 200 is generally heated to a temperature from 400° C. to 800° C. and maintained within this temperature range until the free water and over 90 percent by weight of any bound volatile material are removed. In an optional step, it can be desirable to introduce the modifying additive by an impregnation process. A water-soluble salt can be introduced by impregnation into the pores of the calcined, precursor shaped abrasive particle 100. Then the precursor shaped abrasive particle 100 are pre-fired again.
A further operation can involve sintering the calcined, precursor shaped abrasive particle 100 or 200 to form particles 100 or 200. In some examples where the precursor includes rare earth metals, however, sintering may not be necessary. Prior to sintering, the calcined, precursor shaped abrasive particle 100 or 200 are not completely densified and thus lack the desired hardness to be used as shaped abrasive particle 100 or 200. Sintering takes place by heating the calcined, precursor shaped abrasive particle 100 or 200 to a temperature of from 1000° C. to 1650° C. The length of time for which the calcined, precursor shaped abrasive particle 100 or 200 can be exposed to the sintering temperature to achieve this level of conversion depends upon various factors, but from five seconds to 48 hours is possible.
In another embodiment, the duration of the sintering step ranges from one minute to 90 minutes. After sintering, the shaped abrasive particle 14 can have a Vickers hardness of 10 GPa (gigaPascals), 16 GPa, 18 GPa, 20 GPa, or greater.
Additional operations can be used to modify the described process, such as, for example, rapidly heating the material from the calcining temperature to the sintering temperature, and centrifuging the precursor dispersion to remove sludge and/or waste. Moreover, the process can be modified by combining two or more of the process steps if desired.
Backing 302 can be flexible or rigid. Examples of suitable materials for forming a flexible backing include a polymeric film, a metal foil, a woven fabric, a knitted fabric, paper, vulcanized fiber, a staple fiber, a continuous fiber, a nonwoven, a foam, a screen, a laminate, and combinations thereof. Backing 302 can be shaped to allow coated abrasive article 300 to be in the form of sheets, discs, belts, pads, or rolls. In some embodiments, backing 302 can be sufficiently flexible to allow coated abrasive article 300 to be formed into a loop to make an abrasive belt that can be run on suitable grinding equipment.
Make coat 304 secures shaped abrasive particles 200A to backing 302, and size coat 306 can help to reinforce shaped abrasive particles 200A. Make coat 304 and/or size coat 306 can include a resinous adhesive. The resinous adhesive can include one or more resins chosen from a phenolic resin, an epoxy resin, a urea-formaldehyde resin, an acrylate resin, an aminoplast resin, a melamine resin, an acrylated epoxy resin, a urethane resin, a polyester resin, a dying oil, and mixtures thereof.
Abrasive article 300 can also include conventional (e.g., crushed) abrasive particles. Examples of useful abrasive particles include fused aluminum oxide-based materials such as aluminum oxide, ceramic aluminum oxide (which can include one or more metal oxide modifiers and/or seeding or nucleating agents), and heat-treated aluminum oxide, silicon carbide, co-fused alumina-zirconia, diamond, ceria, titanium diboride, cubic boron nitride, boron carbide, garnet, flint, emery, sol-gel derived abrasive particles, and mixtures thereof.
The conventional abrasive particles can, for example, have an average diameter ranging from about 10 μm to about 2000 μm, about 20 μm to about 1300 μm, about 50 μm to about 1000 μm, less than, equal to, or greater than about 10 μm, 20, 30, 40, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, 1500, 1550, 1650, 1700, 1750, 1800, 1850, 1900, 1950, or 2000 μm. For example, the conventional abrasive particles can have an abrasives industry-specified nominal grade. Such abrasives industry-accepted grading standards include those known as the American National Standards Institute, Inc. (ANSI) standards, Federation of European Producers of Abrasive Products (FEPA) standards, and Japanese Industrial Standard (HS) standards. Exemplary ANSI grade designations (e.g., specified nominal grades) include: ANSI 12 (1842 μm), ANSI 16 (1320 μm), ANSI 20 (905 μm), ANSI 24 (728 μm), ANSI 36 (530 μm), ANSI 40 (420 μm), ANSI 50 (351 μm), ANSI 60 (264 μm), ANSI 80 (195 μm), ANSI 100 (141 μm), ANSI 120 (116 μm), ANSI 150 (93 μm), ANSI 180 (78 μm), ANSI 220 (66 μm), ANSI 240 (53 μm), ANSI 280 (44 μm), ANSI 320 (46 μm), ANSI 360 (30 μm), ANSI 400 (24 μm), and ANSI 600 (16 μm). Exemplary FEPA grade designations include P12 (1746 μm), P16 (1320 μm), P20 (984 μm), P24 (728 μm), P30 (630 μm), P36 (530 μm), P40 (420 μm), P50 (326 μm), P60 (264 μm), P80 (195 μm), P100 (156 μm), P120 (127 μm), P120 (127 μm), P150 (97 μm), P180 (78 μm), P220 (66 μm), P240 (60 μm), P280 (53 μm), P320 (46 μm), P360 (41 μm), P400 (36 μm), P500 (30 μm), P600 (26 μm), and P800 (22 μm). An approximate average particles size of reach grade is listed in parenthesis following each grade designation.
Shaped abrasive particles 100 or 200 or crushed abrasive particles can include any suitable material or mixture of materials. For example, shaped abrasive particles 100 can include a material chosen from an alpha-alumina, a fused aluminum oxide, a heat-treated aluminum oxide, a ceramic aluminum oxide, a sintered aluminum oxide, a silicon carbide, a titanium diboride, a boron carbide, a tungsten carbide, a titanium carbide, a diamond, a cubic boron nitride, a garnet, a fused alumina-zirconia, a sol-gel derived abrasive particle, a cerium oxide, a zirconium oxide, a titanium oxide, and combinations thereof. In some embodiments, shaped abrasive particles 100 or 200 and crushed abrasive particles can include the same materials. In further embodiments, shaped abrasive particles 100 or 200 and crushed abrasive particles can include different materials.
Filler particles can also be included in abrasive articles 200 or 300. Examples of useful fillers include metal carbonates (such as calcium carbonate, calcium magnesium carbonate, sodium carbonate, magnesium carbonate), silica (such as quartz, glass beads, glass bubbles and glass fibers), silicates (such as talc, clays, montmorillonite, feldspar, mica, calcium silicate, calcium metasilicate, sodium aluminosilicate, sodium silicate), metal sulfates (such as calcium sulfate, barium sulfate, sodium sulfate, aluminum sodium sulfate, aluminum sulfate), gypsum, vermiculite, sugar, wood flour, a hydrated aluminum compound, carbon black, metal oxides (such as calcium oxide, aluminum oxide, tin oxide, titanium dioxide), metal sulfites (such as calcium sulfite), thermoplastic particles (such as polycarbonate, polyetherimide, polyester, polyethylene, poly(vinylchloride), polysulfone, polystyrene, acrylonitrile-butadiene-styrene block copolymer, polypropylene, acetal polymers, polyurethanes, nylon particles) and thermosetting particles (such as phenolic bubbles, phenolic beads, polyurethane foam particles and the like). The filler may also be a salt such as a halide salt. Examples of halide salts include sodium chloride, potassium cryolite, sodium cryolite, ammonium cryolite, potassium tetrafluoroborate, sodium tetrafluoroborate, silicon fluorides, potassium chloride, magnesium chloride. Examples of metal fillers include, tin, lead, bismuth, cobalt, antimony, cadmium, iron and titanium. Other miscellaneous fillers include sulfur, organic sulfur compounds, graphite, lithium stearate and metallic sulfides. In some embodiments, individual shaped abrasive particles 100 or individual crushed abrasive particles can be at least partially coated with an amorphous, ceramic, or organic coating. Examples of suitable components of the coatings include, a silane, glass, iron oxide, aluminum oxide, or combinations thereof. Coatings such as these can aid in processability and bonding of the particles to a resin of a binder.
Some shaped abrasive particles 100 or 200 can include a polymeric material and can be characterized as soft abrasive particles. The soft shaped abrasive particles described herein can independently include any suitable material or combination of materials. For example, the soft shaped abrasive particles can include a reaction product of a polymerizable mixture including one or more polymerizable resins. The one or more polymerizable resins such as a hydrocarbyl polymerizable resin. Examples of such resins include those chosen from a phenolic resin, a urea formaldehyde resin, a urethane resin, a melamine resin, an epoxy resin, a bismaleimide resin, a vinyl ether resin, an aminoplast resin (which may include pendant alpha, beta unsaturated carbonyl groups), an acrylate resin, an acrylated isocyanurate resin, an isocyanurate resin, an acrylated urethane resin, an acrylated epoxy resin, an alkyl resin, a polyester resin, a drying oil, or mixtures thereof. The polymerizable mixture can include additional components such as a plasticizer, an acid catalyst, a cross-linker, a surfactant, a mild-abrasive, a pigment, a catalyst and an antibacterial agent.
Where multiple components are present in the polymerizable mixture, those components can account for any suitable weight percentage of the mixture. For example, the polymerizable resin or resins, may be in a range of from about 35 wt % to about 99.9 wt % of the polymerizable mixture, about 40 wt % to about 95 wt %, or less than, equal to, or greater than about 35 wt %, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, or about 99.9 wt %.
If present, the cross-linker may be in a range of from about 2 wt % to about 60 wt % of the polymerizable mixture, from about 5 wt % to about 10 wt %, or less than, equal to, or greater than about 2 wt %, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or about 15 wt %. Examples of suitable cross-linkers include a cross-linker available under the trade designation CYMEL 303 LF, of Annex USA Inc., Alpharetta, Ga., USA; or a cross-linker available under the trade designation CYMEL 385, of Allnex USA Inc., Alpharetta, Ga., USA.
If present, the mild-abrasive may be in a range of from about 5 wt % to about 65 wt % of the polymerizable mixture, about 10 wt % to about 20 wt %, or less than, equal to, or greater than about 5 wt %, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, or about 65 wt %. Examples of suitable mild-abrasives include a mild-abrasive available under the trade designation MINSTRON 353 TALC, of Imerys Talc America, Inc., Three Forks, Mont., USA; a mild-abrasive available under the trade designation USG TERRA ALBA NO. 1 CALCIUM SULFATE, of USG Corporation, Chicago, Ill., USA; Recycled Glass (40-70 Grit) available from ESCA Industries, Ltd., Hatfield, Pa., USA, silica, calcite, nepheline, syenite, calcium carbonate, or mixtures thereof.
If present, the plasticizer may be in a range of from about 5 wt % to about 40 wt % of the polymerizable mixture, about 10 wt % to about 15 wt %, or less than, equal to, or greater than about 5 wt %, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, or about 40 wt %. Examples of suitable plasticizers include acrylic resins or styrene butadiene resins. Examples of acrylic resins include an acrylic resin available under the trade designation RHOPLEX GL-618, of DOW Chemical Company, Midland, Mich., USA; an acrylic resin available under the trade designation HYCAR 2679, of the Lubrizol Corporation, Wickliffe, Ohio, USA; an acrylic resin available under the trade designation HYCAR 26796, of the Lubrizol Corporation, Wickliffe, Ohio, USA; a polyether polyol available under the trade designation ARCOL LG-650, of DOW Chemical Company, Midland, Mich., USA; or an acrylic resin available under the trade designation HYCAR 26315, of the Lubrizol Corporation, Wickliffe, Ohio, USA. An example of a styrene butadiene resin includes a resin available under the trade designation ROVENE 5900, of Mallard Creek Polymers, Inc., Charlotte, N.C., USA.
If present, the acid catalyst may be in a range of from 0.5 wt % to about 20 wt % of the polymerizable mixture, about 5 wt % to about 10 wt %, or less than, equal to, or greater than about 1 wt %, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or about 20 wt %. Examples of suitable acid catalysts include a solution of aluminum chloride or a solution of ammonium chloride.
If present, the surfactant can be in a range of from about 0.001 wt % to about 15 wt % of the polymerizable mixture about 5 wt % to about 10 wt %, less than, equal to, or greater than about 0.001 wt %, 0.01, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or about 15 wt %. Examples of suitable surfactants include a surfactant available under the trade designation GEMTEX SC-85-P, of Innospec Performance Chemicals, Salisbury, N.C., USA; a surfactant available under the trade designation DYNOL 604, of Air Products and Chemicals, Inc., Allentown, Pa., USA; a surfactant available under the trade designation ACRYSOL RM-8W, of DOW Chemical Company, Midland, Mich., USA; or a surfactant available under the trade designation XIAMETER AFE 1520, of DOW Chemical Company, Midland, Mich., USA.
If present, the antimicrobial agent may be in a range of from 0.5 wt % to about 20 wt % of the polymerizable mixture, about 10 wt % to about 15 wt %, or less than, equal to, or greater than about 0.5 wt %, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or about 20 wt %. An example of a suitable antimicrobial agent includes zinc pyrithione.
If present, the pigment may be in a range of from about 0.1 wt % to about 10 wt % of the polymerizable mixture, about 3 wt % to about 5 wt %, less than, equal to, or greater than about 0.1 wt %, 0.2, 0.4, 0.6, 0.8, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, or about 10 wt %. Examples of suitable pigments include a pigment dispersion available under the trade designation SUNSPERSE BLUE 15, of Sun Chemical Corporation, Parsippany, N.J., USA; a pigment dispersion available under the trade designation SUNSPERSE VIOLET 23, of Sun Chemical Corporation, Parsippany, N.J., USA; a pigment dispersion available under the trade designation SUN BLACK, of Sun Chemical Corporation, Parsippany, N.J., USA; or a pigment dispersion available under the trade designation BLUE PIGMENT B2G, of Clariant Ltd., Charlotte, N.C., USA. The mixture of components can be polymerized by curing.
As shown in
The specific z-direction rotational orientation of formed abrasive particles can be achieved through use of a precision apertured screen that positions shaped abrasive particles 100 or 200 into a specific z-direction rotational orientation such that shaped abrasive particle 100 or 200 can only fit into the precision apertured screen in a few specific orientations such as less than or equal to 4, 3, 2, or 1 orientations. For example, a rectangular opening just slightly bigger than the cross section of shaped abrasive particle 100 or 200 comprising a rectangular plate will orient shaped abrasive particle 100 or 200 in one of two possible 180 degree opposed z-direction rotational orientations. The precision apertured screen can be designed such that shaped abrasive particles 100 or 200, while positioned in the screen's apertures, can rotate about their z-axis (normal to the screen's surface when the formed abrasive particles are positioned in the aperture) less than or equal to about 30, 20, 10, 5, 2, or 1 angular degrees.
The precision apertured screen having a plurality of apertures selected to z-directionally orient shaped abrasive particles 100 and 200 into a pattern, can have a retaining member such as adhesive tape on a second precision apertured screen with a matching aperture pattern, an electrostatic field used to hold the particles in the first precision screen or a mechanical lock such as two precision apertured screens with matching aperture patterns twisted in opposite directions to pinch particles 100 and 200 within the apertures. The first precision aperture screen is filled with shaped abrasive particles 100 and 200, and the retaining member is used to hold shaped abrasive particles 100 in place in the apertures. In one embodiment, adhesive tape on the surface of a second precision aperture screen aligned in a stack with the first precision aperture screen causes shaped abrasive particles 100 to stay in the apertures of the first precision screen stuck to the surface of the tape exposed in the second precision aperture screen's apertures.
Following positioning in apertures, coated backing 302 having make layer 304 is positioned parallel to the first precision aperture screen surface containing the shaped abrasive particles 100 or 200 with make layer 304 facing shaped abrasive particles 100 or 200 in the apertures. Thereafter, coated backing 302 and the first precision aperture screen are brought into contact to adhere shaped abrasive particles 100 or 200 to the make layer. The retaining member is released such as removing the second precision aperture screen with taped surface, untwisting the two precision aperture screens, or eliminating the electrostatic field. Then the first precision aperture screen is then removed leaving the shaped abrasive particles 100 or 200 having a specified z-directional rotational orientation on the coated abrasive article 300 for further conventional processing such as applying a size coat and curing the make and size coats.
In the case of a coated abrasive article, the curable binder precursor comprises a make layer precursor, and the magnetizable particles comprise magnetizable abrasive particles. A size layer precursor may be applied over the at least partially cured make layer precursor and the magnetizable abrasive particles, although this is not a requirement. If present, the size layer precursor is then at least partially cured at a second curing station, optionally with further curing of the at least partially cured make layer precursor. In some embodiments, a supersize layer is disposed on the at least partially cured size layer precursor.
Another tool and method to form abrasive article 300 in which shaped abrasive particles 100 or 200 have a specified z-direction rotational angle is to use the system shown in
As shown in
Optionally, filling assist system 1330 is provided after shaped abrasive particle feeder 1320 to move shaped abrasive particles 1302 around on the surface of production tool 1350 and to help orientate or slide shaped abrasive particles 1302 into the cavities 1402. Filling assist system 1330 can be, for example, a doctor blade, a felt wiper, a brush having a plurality of bristles, a vibration system, a blower or air knife, a vacuum box, or combinations thereof. Filling assist system 1330 moves, translates, sucks, or agitates shaped abrasive particles 1302 on dispensing surface 1404 (top or upper surface of production tool 1350 in
After leaving the shaped abrasive particle filling and excess removal section of system 1300, shaped abrasive particles 1302 in production tool 1350 travel towards resin coated backing 1314. Shaped abrasive particle transfer roll 1308 is provided and production tooling 1350 can wrap at least a portion of the roll's circumference. In some embodiments, production tool 1350 wraps between 30 to 180 degrees, or between 90 to 180 degrees of the outer circumference of shaped abrasive particle transfer roll 1308. In some embodiments, the speed of the dispensing surface 1404 and the speed of the resin layer of resin coated backing 1314 are speed matched to each other within ±10 percent, ±5 percent, or ±1 percent, for example.
Various methods can be employed to transfer shaped abrasive particles 1302 from cavities 1402 of production tool 1350 to resin coated hacking 1314. One method includes a pressure assist method where each cavity 1402 in production tooling 1350 has two open ends or the hack surface or the entire production tooling 1350 is suitably porous and shaped abrasive particle transfer roll 1308 has a plurality of apertures and an internal pressurized source of air. With pressure assist, production tooling 1350 does not need to be inverted but it still may be inverted. Shaped abrasive particle transfer roll 1308 can also have movable internal dividers such that the pressurized air can be supplied to a specific arc segment or circumference of the roll to blow shaped abrasive particles 1302 out of the cavities and onto resin coated backing 1314 at a specific location. In some embodiments, shaped abrasive particle transfer roll 1308 may also be provided with an internal source of vacuum without a corresponding pressurized region or in combination with the pressurized region typically prior to the pressurized region as shaped abrasive particle transfer roll 1308 rotates. The vacuum source or region can have movable dividers to direct it to a specific region or are segment of shaped abrasive particle transfer roll 1308. The vacuum can suck shaped abrasive particles 1302 firmly into cavities 1402 as the production tooling 1350 wraps shaped abrasive particle transfer roll 1308 before subjecting shaped abrasive particles 1302 to the pressurized region of shaped abrasive particle transfer roll 1308. This vacuum region be used, for example, with shaped abrasive particle removal member to remove excess shaped abrasive particles 1302 from dispensing surface 1404 or may he used to simply ensure shaped abrasive particles 1302 do not leave cavities 1402 before reaching a specific position along the outer circumference of the shaped abrasive particle transfer roil 1308.
After separating from shaped abrasive particle transfer roll 1308, production tooling 1350 travels along first web path 1304 back towards the shaped abrasive particle filling and excess removal section of the apparatus with the assistance of idler rolls 1310 as necessary. An optional production tool cleaner can be provided to remove stuck shaped abrasive particles still residing in cavities 1402 and/or to remove make coat resin transferred to dispensing surface 1404. Choice of the production tool cleaner can depend on the configuration of the production tooling and could be either alone or in combination, an additional air blast, solvent or water spray, solvent or water bath, an ultrasonic horn, or an idler roil the production tooling wraps to use push assist to farce shaped abrasive particles 1302 out of the cavities 1402. Thereafter production tooling 1350 or belt advances to a shaped abrasive particle filling and excess removal section to he filled with new shaped abrasive particles 1302.
Various idler rolls 1310 can be used to guide the shaped abrasive particle coated backing 1314 having a predetermined, reproducible, non-random pattern of shaped abrasive particles 1302 on the first major surface that were applied by shaped abrasive particle transfer roll 1308 and held onto the first major surface by the make coat resin along second web path 1306 into an oven for curing the make coat resin. Optionally, a second shaped abrasive particle coater can be provided to place additional abrasive particles, such as another type of abrasive particle or diluents, onto the make coat resin prior to entry in an oven. The second abrasive particle coater can be a drop coater, spray coater, or an electrostatic coater as known to those of skill in the art. Thereafter a cured backing with shaped abrasive particles 1302 can enter into an optional festoon along second web path 1306 prior to further processing such as the addition of a size coat, curing of the size coat. and other processing steps known to those of skill in the art of making coated abrasive articles.
Although system 1300 is shown as including production tool 1350 as a belt, it is possible in some alternative embodiments for system 1300 to include production tool 1350 on vacuum pull roll 1308. For example, vacuum pull roll 1308 may include a plurality of cavities 1402 to which shaped abrasive particles 1302 are directly fed. Shaped abrasive particles 1302 can be selectively held in place with a vacuum, which can be disengaged to release shaped abrasive particles 1302 on backing 1314. Further details on system 1300 and suitable alternative may be found at US 2016/0311081, to 3M Company, St. Paul Minn., the contents of which are hereby incorporated by reference.
Although shaped abrasive particles are used as an example, the system 1300 described above may also be used to accurately place non-shaped particles. Due to the configuration of the production tool 1350 placement of particles is very specifically controlled, and may be used to form patterns of a first level, second level, and higher despite the particles themselves not having any pre-determined shape. In one example, a blend of shaped and non-shaped particles may also be used. In selected examples, relatively precise placement of non-shaped particles, using methods and equipment described above may be used to form one or more patterns, in a similar manner to patterns formed through placement of shaped particles of the abrasive article, etc. It is recognized that the example abrasive articles described herein can include precisely-shaped particles, non-shaped particles or a combination thereof.
One or more camouflaging or masking layers can be created on the abrasive article using at least one colored layer to cover a portion of the size coat layer. The at least one colored layer can include one or more colors that are markedly different from a color of the size coat layer. The camouflaging layer can be discontinuous on the abrasive article since it does not cover all of the size coat layer. For purposes herein, the size coat layer can refer to an outermost layer of the abrasive article before the camouflaging layer is applied. In some examples, the abrasive article includes one size coat layer that provides functional grinding properties to the article. In other examples, the abrasive article includes more than one size coat layer that provides functional properties to the article; and in such examples, a second size coat layer can also be referred to as a supersize coat. For purposes herein, the term “size coat” or “size coat layer” can refer to both a single size coat layer and one or more size coat layers.
In some examples, the camouflaging layer can be applied as a repeating pattern of one or more colors on the abrasive article. In some examples, the camouflaging layer can be applied randomly to the abrasive article. The camouflaging layer can be used to mask or minimize an appearance of any imperfections on the abrasive article, such as unfilled or mis-filled particle positions, or to otherwise mask or minimize portions of the abrasive article that are without any particles, such as for example, one or more splices on an abrasive belt. Such design of abrasive articles having a camouflaging or masking layer can be applicable to abrasive articles in the form of sheets, discs, belts, pads, or rolls. Such design can be applicable to coated abrasive articles and non-woven abrasive articles.
In describing a position of the particles relative to other particles, for purposes herein, the term “adjacent” refers to particles that are next to each other in different rows, and the term “neighboring” or “neighbor” refers to particles that are next to each other in the same row. Each particle can be described as having a unique lateral, longitudinal position on the abrasive article. The figures described below include examples of an abrasive article in the form of a disc and a belt. In an example in which the abrasive article is a belt or a sheet, the article can be defined as having one or more longitudinal axes or longitudinal positions, which can be defined relative to a length of the article, and one or more lateral axes or lateral positions, which can be defined relative to a width of the article. In an example, in which the abrasive article is a disc, the disc can similarly be defined for purposes herein as having longitudinal positions that extend radially from a center point of the disc and lateral positions that can be formed by concentric circles formed around the center point of the disc. Concentric circles on the disc can have shared longitudinal positions that create longitudinal rows on the disc.
As shown and described above in reference to
The pattern created by the plurality of particles 1502 on the backing substrate 1504 can comprise a plurality of parallel lines that can be described as longitudinal rows of particles that are generally parallel to the longitudinal axis 1506. The pattern of particles 1502 can also comprise a plurality of parallel lines that can be described as lateral rows of particles that are generally parallel to a lateral axis 1507. In
As shown in
A camouflaging layer or layers, when applied to the abrasive article, may guide or draw the eye away from the micro pattern of the particles 1502. Through use of a camouflaging pattern, the unintended gaps in particle placement and the void 1510 can be masked or downplayed, or otherwise minimized, when the user looks at the belt 1500 as a whole. Examples of different types of camouflaging layers for a coated abrasive article are described below and shown in
The belt 1600 can include a discontinuous layer applied over the size coat layer in a repeating pattern to form a macro pattern on the belt 1600. The discontinuous layer can include a second color that is different than the first color of the size coat layer. The second color can be in high contrast to the first color. In an example, as it is shown in
The diagonal lines 1612 can be oriented on the backing substrate 1604 such that one of the diagonal lines 1612 can overlay a void 1610 on the backing substrate 1604 caused by a splice during processing. The diagonal line 1612 over the void 1610 can mask the absence of particles on the substrate 1604 in the area of the void 1610. Similarly, the other occurrences of the diagonal line 1612 can guide the eye away from the micro pattern of the particles 1602 and mask any unfilled or mis-filled positions on the substrate 1604.
In an example, the discontinuous layer 1612 can be a second size coat layer and provide functional properties to the abrasive article 1600. In other examples, the discontinuous layer 1612 can be a functional or non-functional layer in terms of the abrasive properties (grinding) and abrading performance of the article 1600. Various examples of the discontinuous layer 1612 can provide combinations of functional and non-functional properties, depending on the particle material and how it is applied to the abrasive article 1600. Regardless of whether the discontinuous layer 1612 is functional or not in terms of grinding, the discontinuous layer can provide an aesthetic function to the article 1600. The discontinuous layer 1612 can be applied to the article 1600 using various methods, including those methods used for applying the continuous size coat layer 1608 over the particles 1602. A thickness of the discontinuous layer 1612 on the article 1600 can be generally uniform or vary. The thickness can be such that it provides the above described masking effect, but not too thick that it disrupts the abrading process. In an example, the thickness can be less than 10 centimeters. In an example, the discontinuous layer 1612 can initially be formed as a slurry and then sprayed over the size coat 1608 using a spray coating process. In an example, the discontinuous layer can be applied using lasers and various types of printing (ink-jet, laser-jet, screen printing, etc.).
For the discontinuous layer 1612 to be effective at drawing the eye away from the void 1610 or any unfilled/mis-filled particle positions on the substrate 1604, the discontinuous layer 1612 can be a markedly different color than the first color of the continuous size coat layer. The second color can be described herein as being in high contrast to the first color such that the human eye can register and detect the color difference easily. In an example in which the first color is a drab color, such as a brown or rust color, the second color can be bright in contrast, such as white or silver, for example. In an example in which the first color is black, the second color can be a light or bright color, such as yellow or green.
The first and second color can also be described herein in terms of their respective wavelength on a visible color spectrum. The color spectrum is a portion of the electromagnetic spectrum that is visible to the human eye. Typically, the human eye can see color over wavelengths ranging from about 400 nanometers to 700 nanometers, or alternatively from about 380 nanometers to 800 nanometers. The wavelengths of visible light can be categorized into the following colors—red, orange, yellow, green, blue, indigo and violet. Although different technical sources provide some variability in the wavelength range for each color, an example is included in Table 1 below, as provided from: https://sciencestruck.com/wavelength-of-visible-light-spectrum.
In an example, the first and second colors can be described herein as being separated by a wavelength of at least 100 nm on the visible light spectrum. In other examples, the first and second colors can be separated by a wavelength of at least 150 nm, and in yet other examples, at least 200 nm. In other examples, the colors can be formed by any combination of wavelengths. For purposes herein, when describing the colors of the continuous size coat layer and the discontinuous layer applied to a portion thereof, white and black are also colors.
The belt 1700 can include a discontinuous layer applied over the size coat layer in a repeating pattern to form a macro pattern on the belt 1700. The discontinuous layer can be applied as one or more waves 1712 that can each extend laterally across the belt 1700. The one or more waves 1712 can be formed of a second color that is different than the first color of the size coat layer. Although a void 1710 on the backing substrate 1704 is not completely covered by the waves 1712, the waves 1712 can create a larger pattern on the backing substrate 1704 that can draw the eye away from the void 1710. The waves 1712 can also draw the eye away from any missing particles in the micro pattern of the particles 1702. In other examples, more or less waves 1712 can be included as compared to the two waves 1712 shown in
In another example, the belt can include a discontinuous layer having a second color and a third color. The second color can be applied to the continuous size coat layer as described above. The third color can be applied to the portions of the second color or the third color can be directly applied to the continuous size coat layer. The second and third colors can be applied in the same pattern or in different patterns. For example, referring back to
The discontinuous layer 1812 can be thinly or sparingly applied to the article 1800 such that the discontinuous layer 1812 does not saturate the surface and instead provides partial coverage of the discontinuous layer 1812 on the size coat layer. The specific coverage of the discontinuous layer can vary across the article 1800 such that the color of the size coat is more visible on particular areas of the article 1800 compared to other areas. In an example, a slurry can be created of the material used to form the discontinuous layer 1812 and the slurry can be applied via a spray coat process. Void 1810 is labeled in
In another example, instead of applying the discontinuous layer directly to the size coat layer, the size coat layer (a first continuous layer) can be covered with another continuous, but not necessarily functional layer (a second continuous layer) in terms of grinding. The discontinuous layer can then be applied over a portion of the second continuous layer. In an example, the second continuous layer can be a bright color (such as white) and the discontinuous layer can include one or more colors in high contrast to the color of the second continuous layer. In another example, the size coat layer can include two layers—a first size coat layer and a second size coat layer, which can be also be referred to as a supersize coat layer. The non-functional continuous layer can be applied over the second size coat layer and then the discontinuous layer can be applied over a portion of the non-functional continuous layer.
It is recognized that the abrasive articles described herein, having one or more camouflaging layers, can include any type of pattern or random application of the one or more camouflaging layers to the abrasive article. The one or more camouflaging layers can include a single color that can be in high contrast to the color of the size coat layer. In an example, the camouflaging layers can include two different colors, both of which can be in high contrast to the color of the size coat layer. The second and third colors can also be in high contrast to one another.
The one or more camouflaging layers described herein can be used to mask any imperfections in the particle placement on the backing substrate of an abrasive article. In
The plurality of particles 1902 can be arranged on the disc 1900 such that at least a portion of the particles in the plurality of particles 1902 are aligned longitudinally and laterally relative to other particles 1902 on the disc 1900. The particles 1902 can be attached to the backing substrate 1904 using a continuous size coat layer 1908. A color of the size coat layer 1908 can thus form the color of the disc 1900, at least on the side of the disc 1900 containing the particles 1902. As similar described above in reference to the belt of
The one or more camouflaging layers are described above for use in abrasive articles having particles arranged in patterns. It is recognized that the micro pattern of the particles can extend across some or all of the abrasive article. It is recognized that the one or more camouflaging layers described above can also be used on coated abrasive articles in which some or all of the particles are randomly placed on the abrasive article and the particles are not arranged to form a micro pattern.
It is recognized that
In addition to a coated abrasive article, the one or more camouflaging layers described herein can be applied to a non-woven abrasive article.
In an example, abrasive articles having a camouflaging layer can include precisely-shaped particles, non-shaped particles, or a combination thereof. In an example, the abrasive articles can include coated, shaped abrasive particles and at least a portion of the shaped abrasive articles can have a similar size and geometry. In an example, the shaped abrasive particles can include triangular-shaped particles (described above in detail as an equilateral triangle conforming to a truncated pyramid), tetrahedral-shaped particles or a combination thereof. In an example, the abrasive articles can include non-woven fibers that form a non-woven abrasive article. It is recognized that the camouflaging layer described herein can extend across some or all of the abrasive article.
It is recognized that the one or more camouflaging layers can be applied over particles that can be arranged randomly or in any number of patterns. The particles can be arranged on the backing substrate in lateral alignment, longitudinal alignment or both. The particles can be arranged in a staggered linear pattern. The particles can be arranged in a macro pattern created by one or more micro patterns of the particles and the one or more camouflaging layers can be applied over the macro pattern. Reference is made to co-pending provisional application Ser. No. 62/780,988 filed Dec. 18, 2018, titled “MACRO PATTERN FOR ABRASIVE ARTICLES.”
Various embodiments of the present disclosure can be better understood by reference to the following Examples which are offered by way of illustration. The present disclosure is not limited to the Examples given herein.
Example 1 provides an abrasive article comprising an abrasive material, a continuous size coat layer applied to the abrasive material and covering essentially all of a first side of the abrasive article, and a discontinuous layer applied to a portion of the first side of the abrasive material and covering a corresponding portion of the continuous size coat layer. The continuous size coat layer can comprise a first color. The discontinuous layer can comprise a second color different than the first color.
Example 2 provides the abrasive article of Example 1 optionally configured wherein the discontinuous layer is applied as a repeating pattern on the portion of the abrasive material.
Example 3 provides the abrasive article of Example 1 optionally configured wherein the discontinuous layer is applied randomly on the abrasive material.
Example 4 provides the abrasive article of any one of Examples 1-3 optionally configured wherein the abrasive material comprises a plurality of abrasive particles attached to a backing substrate with an adhesive.
Example 5 provides the abrasive article of Example 4 optionally configured wherein the plurality of abrasive particles are arranged in one or more patterns on the backing substrate, the one or more patterns comprising at least one of longitudinally aligned particles or laterally aligned particles.
Example 6 provides the abrasive article of any one of Examples 1-5 optionally configured wherein the discontinuous layer is a second size coat layer applied over a portion of the continuous size coat layer.
Example 7 provides the abrasive article of any one of Examples 1-6 optionally configured wherein the discontinuous layer comprises a third color different than the first and second colors.
Example 8 provides the abrasive article of any one of Examples 1-3 optionally configured wherein the abrasive material comprises non-woven fibers bonded together with a resin.
Example 9 provides the abrasive article of any one of Examples 1-8 optionally further comprising a continuous intermediate layer applied over the continuous size coat layer, and the discontinuous layer is applied directly over a portion of the continuous intermediate layer.
Example 10 provides the abrasive article of Example 9 optionally configured wherein the continuous intermediate layer comprises a third color different from the first and second colors.
Example 11 provides the abrasive article of any one of Examples 9 or 10 optionally configured wherein the continuous intermediate layer is white.
Example 12 provides the abrasive article of any one of Examples 9-11 optionally configured wherein the second color is a color on a visible light spectrum.
Example 13 provides the abrasive article of any one of Examples 1-2 optionally configured wherein the second color is a high contrast color relative to the first color.
Example 14 provides the abrasive article of Example 13 optionally configured wherein the first color and second color are separated by a wavelength of at least 150 nm on a visible light spectrum.
Example 15 provides an abrasive article comprising a backing substrate, a plurality of particles attached to the backing substrate, an adhesive for attaching the particles to the backing substrate, a continuous size coat layer applied to the plurality of particles and covering essentially all of a first side of the backing substrate, the continuous size coat layer comprising a first color, and a discontinuous layer applied to less than an entirety of the first side of the backing substrate to cover a portion of the size coat layer. The discontinuous layer can comprise a second color different from the first color, and the second color is in high contrast to the first color.
Example 16 provides the abrasive article of Example 15 optionally configured wherein the discontinuous layer is a second size coat layer applied over a portion of the continuous size coat layer.
Example 17 provides the abrasive article of any one of Example 15 or 16 optionally configured wherein the discontinuous layer comprises a third color different from the first and second colors, the third color in high contrast to at least one of the first and second colors.
Example 18 provides the abrasive article of any one of Examples 15-17 optionally configured wherein the discontinuous layer is applied to the first side of the backing substrate in a repeating pattern, and the repeating pattern forms a macro pattern on the abrasive article.
Example 19 provides the abrasive article of any one of Examples 15-18 optionally configured wherein the continuous size coat layer includes a first size coat layer and a second size coat layer applied over the first size coat layer.
Example 20 provides the abrasive article of any one of Examples 15-19 optionally configured wherein the first color is black or white.
Example 21 provides the abrasive article of any one of Examples 15-20 optionally configured wherein the second color is a color on a visible light spectrum.
Example 22 provides the abrasive article of any one of Examples 15-21 optionally configured wherein the first and second colors are colors visible on a visible light spectrum and separated by at least 200 nm on the visible light spectrum.
Example 23 provides the abrasive article of any one of Examples 15-22 optionally configured wherein the plurality of particles are arranged in a repeating pattern on the backing substrate.
Example 24 provides the abrasive article of Example 23 optionally configured wherein the plurality of particles are arranged in longitudinal rows on the backing substrate.
Example 25 provides the abrasive article of Example 24 optionally configured wherein the discontinuous layer comprises a pattern repeating laterally on the backing substrate.
Example 26 provides the abrasive article of any one of Examples 15-22 optionally configured wherein the discontinuous layer is randomly applied to the first side of the backing substrate.
Example 27 provides the abrasive article of any one of Examples 15-26 optionally configured wherein the plurality of particles comprises crushed particles without a precise shape, precisely-shaped particles, and a combination thereof.
Example 28 provides the abrasive article of Example 27 optionally configured wherein at least one of the precisely-shaped particles comprises a first side and a second side separated by a thickness t, the first side comprises a first face having a triangular perimeter and the second side comprises a second face having a triangular perimeter, wherein the thickness t is equal to or smaller than the length of the shortest side-related dimension of the particle.
Example 29 provides the abrasive article of Example 28 optionally further comprising at least one sidewall connecting the first side and the second side.
Example 30 provides the abrasive article of Example 29 optionally configured wherein the at least one sidewall is a sloping sidewall.
Example 31 provides the abrasive article of Example 27 optionally configured wherein at least one of the precisely-shaped particles is tetrahedral and comprises four faces joined by six edges terminating at four tips, each one of the four faces contacting three of the four faces.
Example 32 provides the abrasive article of Example 31 optionally configured wherein at least one of the four faces is substantially planar.
Example 33 provides the abrasive article of any one of Example 31 or 32 optionally configured wherein at least one of the four faces is concave.
Example 34 provides the abrasive article of any one of Examples 31-33 optionally configured wherein at least one of the four faces is convex.
Example 35 provides the abrasive article of any one of Examples 15-34 optionally configured wherein a z-direction rotational angle about a line perpendicular to a major surface of the backing substrate and passing through individual particles of the plurality of particles is substantially the same for a portion of the plurality of particles.
Example 36 provides the abrasive article of any one of Examples 15-35 optionally configured wherein the backing substrate is a belt.
Example 37 provides the abrasive article of any one of Examples 15-35 optionally configured wherein the backing substrate is a disc.
Example 38 provides a method of forming an abrasive article with a camouflaging layer, the method comprising: forming an abrasive article having an abrasive material, applying a continuous size layer to the abrasive material and covering essentially all of a first side of the abrasive article, and applying a discontinuous layer to a portion of the first side of the abrasive article and covering a corresponding portion of the continuous size coat layer. The continuous size coat layer can comprise a first color and the discontinuous layer comprises a second color different than the first color, the second color in high contrast to the first color.
Example 39 provides the method of Example 38 optionally configured wherein forming the abrasive article comprises aligning a plurality of particles in one or more patterns, transferring the one or more patterns to a backing substrate containing a layer of adhesive, and curing the adhesive to attach the plurality of particles to the backing substrate in the one or more patterns.
Example 40 provides the method of Example 39 optionally configured wherein aligning the plurality of particles in one or more patterns comprises aligning the plurality of particles into one or more longitudinal rows and one or more lateral rows.
Example 41 provides the method of any one of Examples 38-40 optionally configured wherein forming the abrasive article comprises bonding a plurality of non-woven fibers together with a resin to form a non-woven abrasive article.
Example 42 provides the method of any one of Examples 38-41 optionally configured wherein applying the discontinuous layer to a portion of the first side of the abrasive article comprises applying the discontinuous layer in a repeating pattern, and the repeating pattern forms a macro pattern on the abrasive article.
Example 43 provides the method of any one of Example 38-41 optionally configured wherein applying the discontinuous layer to a portion of the first side of the abrasive article comprises randomly applying the discontinuous layer to the abrasive article.
Example 44 provides an article or method of any one or any combination of Examples 1-43, which can be optionally configured such that all steps or elements recited are available to use or select from.
The terms and expressions that have been employed are used as terms of description and not of limitation, and there is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the embodiments of the present disclosure. Thus, it should be understood that although the present disclosure has been specifically disclosed by specific embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those of ordinary skill in the art, and that such modifications and variations are considered to be within the scope of embodiments of the present disclosure.
Various aspects of the disclosure have been described. These and other aspects are within the scope of the following claims.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2019/060954 | 12/17/2019 | WO | 00 |
Number | Date | Country | |
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62781108 | Dec 2018 | US |