US2426441A - Manufacture of abrasive materials - Google Patents
Manufacture of abrasive materials Download PDFInfo
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- US2426441A US2426441A US567119A US56711944A US2426441A US 2426441 A US2426441 A US 2426441A US 567119 A US567119 A US 567119A US 56711944 A US56711944 A US 56711944A US 2426441 A US2426441 A US 2426441A
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- emery
- resin
- fillet
- coating
- fabric
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D11/00—Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
- B24D11/001—Manufacture of flexible abrasive materials
- B24D11/005—Making abrasive webs
Definitions
- This invention relates to improvements in the- -manufacture of emery fillet, especially grooved emery fillet.
- Emery'fillet consisting of narrow fabric coated on one side with an abrasive such as emery, garnet or corundum, is employed ,for winding on cylinders or rollers to serve for the grinding of card clothing on cylinders and dofiers, carding machines or the like.
- Card clothing which is'used on cylinders, doffers, carding machines and the like in the textile industry is customarily subjected to what is termed "grinding after manufacture and at intervals during its use.
- grinding the tips of the wires are brought into light contact with an abrasive material, such as emery, secured to the face of a roller or cylinder which is rotated and may be traversed over the work.
- One method of making such a card grinding cylinder or roller consists in winding the material known as emery fillet around the roller and securing it in position so as to provide a substantially unbroken area of abrasive material on the surface of the roller.
- One method of'manufacturing emery fillet is to take a narrow woven fabric. of cotton, linen, or cotton and linen, apply to one face a preparation of animal glue and cause emery powder to be adhered to the glue and then allow it to dry.
- Such longitudinal grooving is known to be valuable in emery fillet but its best eflect is exhibited on double coated fillet.
- a further layer of animal glue is applied to the first layer before'grooving and a further coating of emery powder caused to adhere thereto whereafter the double coating is grooved and allowed to dry.
- plastic or plasticised synthetic resin as the adhesive for the abrasive powder, a plastic or plasticised synthetic resin.
- plasticised ureaformaldehyde resins especially combinations .of urea-formaldehyde resins, and alkyd resins are particularly useful for this purpose.
- the synthetic resin composition chosen must be such that it does not undergo any undesirable alteration in hardness or adhesive properties under any atmospheric conditions likely to be encountered during storage. Synthetic resins are in general unaffected by moisture and in order to avoid embrittlement at low temperatures it is necessary either to employ a thermoplastic resin which has a high degree of flexibility at low temperatures or to employ a plasticised resin which may be of the thermoplastic or thermosetting type. I
- the synthetic resin composition Whether the synthetic resin composition penetrates the composition or not, it must be sufflciently flexible to enable the coating to bend without detachment from the support and without breaking away of the adhesive when the fillet is wound on a cylinder or roller and to enable it to stand the grooving operation. 4
- thermo-hardening resins tend to suffer less change in plasticity under changes of atmospherical temperature. It is preferred, however, to use a preparation which can be cured at a fairly low temperature, i. e. below 212 F. and preferably at or only a little above atmospheric temperature.
- thermo-hardening resin it is essential to avoid the use of such long times and/or high temperatures of heating that brittleness develops. If this occurs, the emery fillet may. crack when wound on the cylinders and/or the abrasive may easily rub off. The time,
- urea-formaldehyde resins suitable for use in practicing the present invention especially when piasticised with allwd resins.
- the invention is not limited to these since other resins may be used, for example, melamine formaldehyde products.
- I use the expression synthetic" resin in a broad sense as including artificialcondensation products such as phenol formaldehyde products, urea and thiourea formaldehyde products, po1ybasic-acid-polyhydric-alcohol condensation products, amine formaldehyde condensation products and the like, polymerisation products such as polyvinyl halides, polyvinyl esters, polystyrene derivatives, polymerised acrylic acid esters, and the like, as well as plastic materials of the type of cellulose esters such as cellulose acetate and cellulose nitrate.
- artificialcondensation products such as phenol formaldehyde products, urea and thiourea formaldehyde products, po1ybasic-acid-polyhydric-alcohol condensation products, amine formaldehyde condensation products and the like
- polymerisation products such as polyvinyl halides, polyvinyl esters, polystyrene derivatives, polymerised acrylic acid
- thermoplastic material especially cellulose acetate and polyvinyl esters
- thermoplastic material do not readily wet the particles of emery and satisfactory adhe sion of the emery can be secured only by mixing it with the thermoplastic material before coating. This involves difilculties in spreading the material on the narrow fabric base, which are particularly noticeable with the extremely coarse abrasives I used in emery fillet, and accordingly mixing of the abrasive with the adhesive before coating is less preferable.
- One suitable composition which can be used consists of a mixture of urea-formaldehyde resin such as that sold under the trade name of Resin U. G., and of alkyd resin such as that sold under the trade name of Resin R. P. 8 in the proportion of one part of the former to two of the latter.
- a known acidic hardening agent By the incorporation of a known acidic hardening agent into this mixture hardening can be effected at temperatures below 212 F. and even below 100 F., e. g. at room temperatures.
- the alkyd resin serves as a plasticiser for the ureaformaldehyde resin and gives a bonding agent which is sufllciently flexible to furnish an emery fillet of the same degree offlexlbility as that obtained with the customary animal glue preparations.
- Suitable resin compositions are (a) that sold by British Resin Products under the trade name Epok, which is an oil-modified phenolic resin dissolved in xylol (70% resin), (b) a mixture of equal proportions of the resins sold by I. C. I. under the trade names "Paralac 100,” and "Paralac 2851!.” These are Glyptal resins. (c) That sold by British Resin Products under the trade name Distrene. This is a polystyrene resin.
- Fig. 1 shows an elevation of a roll of emery fillet made in accordance with this invention
- Fig. 2 shows on a larger scale a plan view of the coated side of a part of the emery fillet shown in Fig. 1,
- Fig. 3 is a side sectional elevation on a. still larger scale of the emery fillet shown in Fig, 1.
- the narrow textile fabric support i carries a flexible coating 2 composed of an alkyd resin piasticised ureaformaldehyde resin adhered to which are coarse emery particles 3.
- the coating 2 is formed of ms separately applied layers In. and 2b identical in composition. They are shown, for convenience,
- Example 1 An etherified urea-formaldehyde resin plasticised with an alkyd resin dissolved in butyl alcohoi.
- the urea-formaldehyde resin is one made by condensing one molecular proportion of urea with three molecular proportions of formaldehyde in the presence of butyl alcohol, the mixture being on the alkaline side of neutrality and heated under reflux at 100 C. for one hour. At the end of this time the mixture is acidified and the water boiled oil. as an azeotropic mixture with butyl alcohol, leaving the etherified resin in butyl alcohol solution.
- the alkyd resin is made by heating a. mixture of 148 parts by weight of phthalic anhydride, 47 parts by weight of glycerol, 15 parts by weight of glycol and 152 parts by weight of castor oil, under reflux allowing escape of water in an inert atmosphere at 420 F. for 6 to 8 hours until a suitable acid value and viscosity are obtained.
- the narrow fabric is wound spirally on to a cylinder so as to cover the surface thereof. It is then painted by brushing or spraying with a solution of resinous material in a solvent. Then a coating of emery particles of any suitable fineness is dusted on. While the coating is still plastic the cylinder is revolved in contact with a ribbed roller having, for example, twelve ribs to the inch, each rib about one-sixteenth of an inch deep. This produces grooves in the coating along the length of the fabric. The coating is then allowed to dry with heating if necessary (e. g. to about 100 F.) preferably with warm air, in order to dry oil the solvent and harden the resin it this is of the thermo-hardening or polymerisable type. Finally, the emery fillet is unwound from the cylinder and made up into rolls. I
- Example 2 An ammonia catalysed cresol-iforrnaldehyde resin made by condensing 1 molecular proportion of 60% metacresol with 1.4 molecular proportions of formaldehyde using 0.05% by weight of 0.880 ammonia (calculated on the cresol) as catalyst.
- Example 3 Parts by weight Phthalic anhydride 15o Glycerol Castor i Example 4.
- Polystyrene Purified monomeric styrene is polymerised alone or in aqueous emulsion by heating at 100- 160 C. in the presence of 0.1 to 1% of an oxidation catalyst such as benzoyl peroxide. The molecularweight of the product obtained is higher or lower according to whether the concentration of catalyst and/or the temperature is higher or lower.
- an oxidation catalyst such as benzoyl peroxide
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Polishing Bodies And Polishing Tools (AREA)
Description
1947- s. w. DRONSFIELD 2,426,441
' MANUFACTURE OF ABRASIVE MATER IALS Filed Dec. 7, 1944 INVENTOR. bYZuavI /EZ I store it under conditions Patented Aug. 26, 1947 MANUFACTURE OF ABBASIVE MATERIALS Samuel Wilkinson Dronsfield, Wilmslow, England Application December 7, 1944, Serial No.
In Great Britain January 1, 194 4 1 Claim. (01. 51-185) This invention relates to improvements in the- -manufacture of emery fillet, especially grooved emery fillet.
Emery'fillet, consisting of narrow fabric coated on one side with an abrasive such as emery, garnet or corundum, is employed ,for winding on cylinders or rollers to serve for the grinding of card clothing on cylinders and dofiers, carding machines or the like.
Card clothing which is'used on cylinders, doffers, carding machines and the like in the textile industry is customarily subjected to what is termed "grinding after manufacture and at intervals during its use. In such grinding the tips of the wires are brought into light contact with an abrasive material, such as emery, secured to the face of a roller or cylinder which is rotated and may be traversed over the work.
One method of making such a card grinding cylinder or roller consists in winding the material known as emery fillet around the roller and securing it in position so as to provide a substantially unbroken area of abrasive material on the surface of the roller.
One method of'manufacturing emery fillet is to take a narrow woven fabric. of cotton, linen, or cotton and linen, apply to one face a preparation of animal glue and cause emery powder to be adhered to the glue and then allow it to dry. This gives a fillet having a thin coating of abrasive which can be wound on cylinders and rollers and gives useful results in many cases. It is better, however, before allowing the coating to dry, to provide the material with longitudinal grooves, for example by passing it into contact with the face of a'grooved roller. Such longitudinal grooving is known to be valuable in emery fillet but its best eflect is exhibited on double coated fillet. In the case of such double coated fillet, a further layer of animal glue is applied to the first layer before'grooving and a further coating of emery powder caused to adhere thereto whereafter the double coating is grooved and allowed to dry.
Although preparations of animal glue are satisfactory as adhesives when the material is in use, there is a risk of double coated grooved emery fillet becoming too hard or too soft during storage owing to changes in atmospheric conditions. Frequently it is necessary to store such emery-fillet under conditions of high temperature and humidity, as for example in India, or 'to of low temperature and/or'low humidity. If the maerial becomes unduly softened it may be spoiled and if it be- 2 comes unduly hard it may crack or break when an attempt is made to wind it on the card grinding rollers or cylinders.
I have found that these difliculties can be overcome by employing as the adhesive for the abrasive powder, a plastic or plasticised synthetic resin. I have further found that plasticised ureaformaldehyde resins, especially combinations .of urea-formaldehyde resins, and alkyd resins are particularly useful for this purpose.
Certain precautionshave to be observed, how'- ever, when using plasticised synthetic resins as adhesives for the abrasive powder in making grooved emery fillet, especially double coated,
grooved emery fillet.
1. The synthetic resin composition chosen must be such that it does not undergo any undesirable alteration in hardness or adhesive properties under any atmospheric conditions likely to be encountered during storage. Synthetic resins are in general unaffected by moisture and in order to avoid embrittlement at low temperatures it is necessary either to employ a thermoplastic resin which has a high degree of flexibility at low temperatures or to employ a plasticised resin which may be of the thermoplastic or thermosetting type. I
2. It is important to avoid stiffening of the fabric. This involves the use of a resin composition which, if it penetrates the fabric, is highly flexible. I
3. Whether the synthetic resin composition penetrates the composition or not, it must be sufflciently flexible to enable the coating to bend without detachment from the support and without breaking away of the adhesive when the fillet is wound on a cylinder or roller and to enable it to stand the grooving operation. 4
In the practice of the present invention it is preferred to employ a plasticised thermo-hardening resin since thermo-hardening resins tend to suffer less change in plasticity under changes of atmospherical temperature. It is preferred, however, to use a preparation which can be cured at a fairly low temperature, i. e. below 212 F. and preferably at or only a little above atmospheric temperature. When using thermo-hardening resin it is essential to avoid the use of such long times and/or high temperatures of heating that brittleness develops. If this occurs, the emery fillet may. crack when wound on the cylinders and/or the abrasive may easily rub off. The time,
and temperature of heating must be such that the synthetic. resin is no longer sticky but is quite firm, flexible and water-resistant. 1
As already stated, I have found urea-formaldehyde resins suitable for use in practicing the present invention especially when piasticised with allwd resins. The invention, however, is not limited to these since other resins may be used, for example, melamine formaldehyde products. I use the expression synthetic" resin, however, in a broad sense as including artificialcondensation products such as phenol formaldehyde products, urea and thiourea formaldehyde products, po1ybasic-acid-polyhydric-alcohol condensation products, amine formaldehyde condensation products and the like, polymerisation products such as polyvinyl halides, polyvinyl esters, polystyrene derivatives, polymerised acrylic acid esters, and the like, as well as plastic materials of the type of cellulose esters such as cellulose acetate and cellulose nitrate. It has been found, however, that most of the thermoplastic material, especially cellulose acetate and polyvinyl esters, do not readily wet the particles of emery and satisfactory adhe sion of the emery can be secured only by mixing it with the thermoplastic material before coating. This involves difilculties in spreading the material on the narrow fabric base, which are particularly noticeable with the extremely coarse abrasives I used in emery fillet, and accordingly mixing of the abrasive with the adhesive before coating is less preferable.
One suitable composition which can be used consists of a mixture of urea-formaldehyde resin such as that sold under the trade name of Resin U. G., and of alkyd resin such as that sold under the trade name of Resin R. P. 8 in the proportion of one part of the former to two of the latter. By the incorporation of a known acidic hardening agent into this mixture hardening can be effected at temperatures below 212 F. and even below 100 F., e. g. at room temperatures. The alkyd resin serves as a plasticiser for the ureaformaldehyde resin and gives a bonding agent which is sufllciently flexible to furnish an emery fillet of the same degree offlexlbility as that obtained with the customary animal glue preparations.
Other suitable resin compositions are (a) that sold by British Resin Products under the trade name Epok, which is an oil-modified phenolic resin dissolved in xylol (70% resin), (b) a mixture of equal proportions of the resins sold by I. C. I. under the trade names "Paralac 100," and "Paralac 2851!." These are Glyptal resins. (c) That sold by British Resin Products under the trade name Distrene. This is a polystyrene resin.
The general procedure in making emery fillet material is applied over the emery treated covering before grooving and a further quantity of emery particles applied.
In the accompanying drawings:
Fig. 1 shows an elevation of a roll of emery fillet made in accordance with this invention,
Fig. 2 shows on a larger scale a plan view of the coated side of a part of the emery fillet shown in Fig. 1,
Fig. 3 is a side sectional elevation on a. still larger scale of the emery fillet shown in Fig, 1.
As shown in the drawings, the narrow textile fabric support i carries a flexible coating 2 composed of an alkyd resin piasticised ureaformaldehyde resin adhered to which are coarse emery particles 3.
As efio wn in Fig. 3, the coating 2 is formed of ms separately applied layers In. and 2b identical in composition. They are shown, for convenience,
as separated by a line but they form together a unitary coating which is longitudinally grooved as shown at inFig. 2.
Examples of resinous compositions which may be used will now be given.
Example 1 An etherified urea-formaldehyde resin plasticised with an alkyd resin dissolved in butyl alcohoi.
The urea-formaldehyde resin is one made by condensing one molecular proportion of urea with three molecular proportions of formaldehyde in the presence of butyl alcohol, the mixture being on the alkaline side of neutrality and heated under reflux at 100 C. for one hour. At the end of this time the mixture is acidified and the water boiled oil. as an azeotropic mixture with butyl alcohol, leaving the etherified resin in butyl alcohol solution.
The alkyd resin is made by heating a. mixture of 148 parts by weight of phthalic anhydride, 47 parts by weight of glycerol, 15 parts by weight of glycol and 152 parts by weight of castor oil, under reflux allowing escape of water in an inert atmosphere at 420 F. for 6 to 8 hours until a suitable acid value and viscosity are obtained.
'1 parts by weight of each of the above resins is dissolved in 5 parts by weight of xylene and 1 according to the present invention is as follows:
The narrow fabric is wound spirally on to a cylinder so as to cover the surface thereof. It is then painted by brushing or spraying with a solution of resinous material in a solvent. Then a coating of emery particles of any suitable fineness is dusted on. While the coating is still plastic the cylinder is revolved in contact with a ribbed roller having, for example, twelve ribs to the inch, each rib about one-sixteenth of an inch deep. This produces grooves in the coating along the length of the fabric. The coating is then allowed to dry with heating if necessary (e. g. to about 100 F.) preferably with warm air, in order to dry oil the solvent and harden the resin it this is of the thermo-hardening or polymerisable type. Finally, the emery fillet is unwound from the cylinder and made up into rolls. I
If desired, a further coating of the resinous part by weight of an acid organic ester of phcs-- phoric acid is added to accelerate the hardening.
Example 2 An ammonia catalysed cresol-iforrnaldehyde resin made by condensing 1 molecular proportion of 60% metacresol with 1.4 molecular proportions of formaldehyde using 0.05% by weight of 0.880 ammonia (calculated on the cresol) as catalyst.
Example 3 Parts by weight Phthalic anhydride 15o Glycerol Castor i Example 4. Polystyrene Purified monomeric styrene is polymerised alone or in aqueous emulsion by heating at 100- 160 C. in the presence of 0.1 to 1% of an oxidation catalyst such as benzoyl peroxide. The molecularweight of the product obtained is higher or lower according to whether the concentration of catalyst and/or the temperature is higher or lower.
I declare that what I claim is:
The method of making a flexible, substantially longitudinally grooved emery fillet capable of being wound around a cylindrical roller to provide a substantially unbroken circumferentially grooved area of abrasive material on the surface thereof which will serve for the grinding of card clothing, which consists in wrapping a narrow textile fabric around a. cylinder to cover the surface thereof, applying to the exposed face of said fabric a first solution in volatile solvent of an alkyd resin plasticised urea formaldehyde resin capable of'being cured at a temperature below 212 F.,
dusting coarse emery particles on the coating formed by said first solution, applying to said coating 9. second solution in volatile solvent of an alkyd resin plasticlsed urea formaldehyde resin capable of being cured at a temperature below 212 F. dusting further coarse emery particles on the combined coating of saidflrst and second solutions, revolving the cylinder carrying said cure the resin and finally removing the coate fabric'with the coated surface of said contact with a ribbed roller to produce complementary grooving in the combined coating on' said fabric, bringing the coated fabric into contact with warm air to remove all solvent and fabric from said cylinder.
SAMUEL WILKINSON DRONSFIELD.
REFERENCES crrEn UNITED STATES PATENTS Number Name Date 875,936 Landis Jan. 7, 1908 1,414,447 Tone May 2, 1922 1,657,784 Bergstrom Jan. 31, 1928 328,004 Church Oct, 13, 1885 592,992 Lowry et a1 Nov. 2, 1897 804,514 Wysong Nov. 14, 1905 1,194,494 Freeman Aug. 15, 1916 942,808 Baekeland Dec; 7, 1909 1,537,454 Brock May 12, 1925 1,576,122 Webster Mar. 9, 1926 1,900,386 Kuzmick Mar. 7, 1933 1,901,325 Novotny Mar, 14, 1933 Re. 21,737 Kistler i Mar. 4, 1941 Re.21,738 Kistler Mar. 4, 1941 1,775,631 Carlton Sept. 16, 1930 2,078,831 Benner et al Apr. 27, 1937 2,230,934 Carlton etal. Feb. 4, 1941 604,569 Ringstrom May 24, 1898 302,652 Decker July 29, 1884 2,268,663 Kuzmi'ck Jan. 6, 1942 2,184,293 Edgar et al. Dec. 26, 1939 2,242,877 Albertson May 20, 1941 FOREIGN PATENTS Number Country Date Sweden Apr. 30, 1941 fabric in
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GB2426441X | 1944-01-01 |
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US2426441A true US2426441A (en) | 1947-08-26 |
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US567119A Expired - Lifetime US2426441A (en) | 1944-01-01 | 1944-12-07 | Manufacture of abrasive materials |
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US (1) | US2426441A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2609642A (en) * | 1947-07-14 | 1952-09-09 | Osborn Mfg Co | Brush and brush material |
US2755607A (en) * | 1953-06-01 | 1956-07-24 | Norton Co | Coated abrasives |
US2860960A (en) * | 1953-11-10 | 1958-11-18 | Abrasive And Metal Products Co | Abrasive articles and method for making the same |
US3073716A (en) * | 1957-11-08 | 1963-01-15 | Truly Magic Products Inc | Method of making a cleaning pad |
US3353308A (en) * | 1963-06-04 | 1967-11-21 | Zane Riccardo | Flexible abrasive disc |
Citations (23)
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US302652A (en) * | 1884-07-29 | Wilhelm deckeb | ||
US328004A (en) * | 1885-10-13 | Polishing or emery cord | ||
US592992A (en) * | 1897-11-02 | Sandpapering-machine | ||
US604569A (en) * | 1898-05-24 | Strom | ||
US804514A (en) * | 1904-11-05 | 1905-11-14 | Olmedo Cortez Wysong | Abrasive apparatus. |
US875936A (en) * | 1907-07-30 | 1908-01-07 | Ezra F Landis | Abrading material. |
US942808A (en) * | 1907-10-26 | 1909-12-07 | Leo H Baekeland | Abrasive composition and method of making same. |
US1194494A (en) * | 1916-08-15 | Assigwqb to lottis g | ||
US1414447A (en) * | 1920-05-20 | 1922-05-02 | Carborundum Co | Abrasive coated sheet and method of making the same |
US1537454A (en) * | 1922-12-11 | 1925-05-12 | Bakelite Corp | Abrasive implement and method of making same |
US1576122A (en) * | 1924-02-04 | 1926-03-09 | Norton Co | Abrasive article |
US1657784A (en) * | 1925-11-23 | 1928-01-31 | Gustave A Bergstrom | Abrasive-covered material and the like |
US1775631A (en) * | 1926-03-13 | 1930-09-16 | Minnesota Mining & Mfg | Abrasive article and method of making the same |
US1900386A (en) * | 1929-06-24 | 1933-03-07 | Manhattan Rubber Mfg Division | Abrasive product and method of making the same |
US1901325A (en) * | 1929-09-06 | 1933-03-14 | John Stogdell Stokes | Abrasive body and method of making the same |
US2078831A (en) * | 1935-12-30 | 1937-04-27 | Carborundum Co | Production of abrasive material |
US2184293A (en) * | 1936-10-08 | 1939-12-26 | Du Pont | Abrasive |
US2230934A (en) * | 1934-01-27 | 1941-02-04 | Minnesota Mining & Mfg | Waterproof sandpaper |
USRE21738E (en) * | 1941-03-04 | Resin bonded abrasive article | ||
USRE21737E (en) * | 1941-03-04 | Resin bonded abrasive article | ||
US2242877A (en) * | 1939-03-15 | 1941-05-20 | Albertson & Co Inc | Abrasive disk and method of making the same |
SE101940C1 (en) * | 1939-07-26 | 1941-07-01 | ||
US2268663A (en) * | 1939-09-19 | 1942-01-06 | J K Smit & Sons Inc | Abrasive tool |
-
1944
- 1944-12-07 US US567119A patent/US2426441A/en not_active Expired - Lifetime
Patent Citations (23)
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---|---|---|---|---|
USRE21738E (en) * | 1941-03-04 | Resin bonded abrasive article | ||
US328004A (en) * | 1885-10-13 | Polishing or emery cord | ||
US592992A (en) * | 1897-11-02 | Sandpapering-machine | ||
US604569A (en) * | 1898-05-24 | Strom | ||
US1194494A (en) * | 1916-08-15 | Assigwqb to lottis g | ||
US302652A (en) * | 1884-07-29 | Wilhelm deckeb | ||
USRE21737E (en) * | 1941-03-04 | Resin bonded abrasive article | ||
US804514A (en) * | 1904-11-05 | 1905-11-14 | Olmedo Cortez Wysong | Abrasive apparatus. |
US875936A (en) * | 1907-07-30 | 1908-01-07 | Ezra F Landis | Abrading material. |
US942808A (en) * | 1907-10-26 | 1909-12-07 | Leo H Baekeland | Abrasive composition and method of making same. |
US1414447A (en) * | 1920-05-20 | 1922-05-02 | Carborundum Co | Abrasive coated sheet and method of making the same |
US1537454A (en) * | 1922-12-11 | 1925-05-12 | Bakelite Corp | Abrasive implement and method of making same |
US1576122A (en) * | 1924-02-04 | 1926-03-09 | Norton Co | Abrasive article |
US1657784A (en) * | 1925-11-23 | 1928-01-31 | Gustave A Bergstrom | Abrasive-covered material and the like |
US1775631A (en) * | 1926-03-13 | 1930-09-16 | Minnesota Mining & Mfg | Abrasive article and method of making the same |
US1900386A (en) * | 1929-06-24 | 1933-03-07 | Manhattan Rubber Mfg Division | Abrasive product and method of making the same |
US1901325A (en) * | 1929-09-06 | 1933-03-14 | John Stogdell Stokes | Abrasive body and method of making the same |
US2230934A (en) * | 1934-01-27 | 1941-02-04 | Minnesota Mining & Mfg | Waterproof sandpaper |
US2078831A (en) * | 1935-12-30 | 1937-04-27 | Carborundum Co | Production of abrasive material |
US2184293A (en) * | 1936-10-08 | 1939-12-26 | Du Pont | Abrasive |
US2242877A (en) * | 1939-03-15 | 1941-05-20 | Albertson & Co Inc | Abrasive disk and method of making the same |
SE101940C1 (en) * | 1939-07-26 | 1941-07-01 | ||
US2268663A (en) * | 1939-09-19 | 1942-01-06 | J K Smit & Sons Inc | Abrasive tool |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2609642A (en) * | 1947-07-14 | 1952-09-09 | Osborn Mfg Co | Brush and brush material |
US2755607A (en) * | 1953-06-01 | 1956-07-24 | Norton Co | Coated abrasives |
US2860960A (en) * | 1953-11-10 | 1958-11-18 | Abrasive And Metal Products Co | Abrasive articles and method for making the same |
US3073716A (en) * | 1957-11-08 | 1963-01-15 | Truly Magic Products Inc | Method of making a cleaning pad |
US3353308A (en) * | 1963-06-04 | 1967-11-21 | Zane Riccardo | Flexible abrasive disc |
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