USRE21737E - Resin bonded abrasive article - Google Patents
Resin bonded abrasive article Download PDFInfo
- Publication number
- USRE21737E USRE21737E US21737DE USRE21737E US RE21737 E USRE21737 E US RE21737E US 21737D E US21737D E US 21737DE US RE21737 E USRE21737 E US RE21737E
- Authority
- US
- United States
- Prior art keywords
- acrylic acid
- abrasive
- bonded
- acid
- alpha
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000005296 abrasive Methods 0.000 title description 11
- 239000011347 resin Substances 0.000 title description 11
- 229920005989 resin Polymers 0.000 title description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 15
- 239000000203 mixture Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 9
- VVQNEPGJFQJSBK-UHFFFAOYSA-N 2-methyl-2-propenoic acid methyl ester Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
- 239000006061 abrasive grain Substances 0.000 description 8
- 229940063559 methacrylic acid Drugs 0.000 description 8
- 238000006467 substitution reaction Methods 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- VZGDMQKNWNREIO-UHFFFAOYSA-N Carbon tetrachloride Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 229920003002 synthetic resin Polymers 0.000 description 5
- 239000000057 synthetic resin Substances 0.000 description 5
- 239000004342 Benzoyl peroxide Substances 0.000 description 4
- OMPJBNCRMGITSC-UHFFFAOYSA-N Incidol Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 4
- 235000019400 benzoyl peroxide Nutrition 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 125000005395 methacrylic acid group Chemical group 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 229920001800 Shellac Polymers 0.000 description 2
- 150000001253 acrylic acids Chemical class 0.000 description 2
- -1 allyl ester Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- HTEAGOMAXMOFFS-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C HTEAGOMAXMOFFS-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000004208 shellac Substances 0.000 description 2
- 229940113147 shellac Drugs 0.000 description 2
- 235000013874 shellac Nutrition 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- RWHRFHQRVDUPIK-UHFFFAOYSA-N 50867-57-7 Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O RWHRFHQRVDUPIK-UHFFFAOYSA-N 0.000 description 1
- XXROGKLTLUQVRX-UHFFFAOYSA-N Allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N Boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KAZBKCHUSA-N D-Mannitol Natural products OC[C@@H](O)[C@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KAZBKCHUSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N Silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N Tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N Triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N Trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N Tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- BHBPJIPGXGQMTE-UHFFFAOYSA-N ethane-1,2-diol;2-methylprop-2-enoic acid Chemical compound OCCO.CC(=C)C(O)=O.CC(=C)C(O)=O BHBPJIPGXGQMTE-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000002223 garnet Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 125000005468 isobutylenyl group Chemical group 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229910052904 quartz Inorganic materials 0.000 description 1
- 230000001105 regulatory Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B35/00—Machines or devices designed for superfinishing surfaces on work, i.e. by means of abrading blocks reciprocating with high frequency
Definitions
- the invention relates to abrasive articles bonded ,with modified polymers of acrylic acid and substituted acrylic acids in which the substituent is either methyl or chlorine and their derivatives.
- One object of the invention is to provide an abrasive article bonded with a hard resin of the class indicated. Another object of the invention is to provide an abrasive article bonded with a heat resistant resin of the class indicated, preferably softening above 100 C. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having some of the characteristics of shellacv bonded grinding wheels. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin, having some of the characteristics of rubber. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having characteristics superior to either those of shellac or rubber for certain purposes and capable of substantial duplication in its physical properties. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having definite characteristics advantageous for the manufacture of grinding wheels.
- Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having one or more of the following characteristics: Soft as compared with phenol-formaldehyde, readily controllable, resistant to heat as compared with shellac and rubber, and capable of being made in different degrees of hardness.
- esters of acrylic acid and substituted acrylic acids for example alpha methyl acrylic acid and alpha chloro acrylic acid
- polyhydric alcohols we mention ethylene glycol, diethylene glycol, triethylene glycol, glycerol, Pentaglycerol, trimethyleneglycol, pentaerythritol, and mannitol.
- Another suitable substance which contains more than one unsaturated group per molecule is an allyl ester of acrylic or the alpha substituted acrylic acid.
- a grinding wheel consists of abrasive grain bonded with a given bond which holds the individual grains together in the form of an integral wheel.
- Other abrasive bodies such as bricks, segments and the like are to be deemed included within the following description and the methods and substances indicated may be used for the manufacture of other abrasive wheels, such as lapping wheels, regulating wheels and the like.
- abrasive we may use any of the usual or known types, such as any yariety of alumina, e. g., fused alumina, emery and corundum, and we may also use silicon carbide or diamonds.
- abrasives such as garnet, quartz, and any of the hard carbides, for example boron carbide or tungsten carbide, might be employed.
- resins may be produced as the copolymers of methyl methacrylate with methacrylic acid and one or more of the esters of methacrylic acid and a'polyhydric alcohol or allyl alcohol, as hereinbefore set forth.
- Our novel resin constitutes on the one hand the copolymerization product of acrylic acid or its alpha substitution products in which the substituent is either methyl or chlorine with monohydric alcohol esters of acrylic acid or the alpha substitution products and, on the other hand, the copolymerization product of acrylic acid or the alpha substitution products with monohydric alcohol esters of acrylic acid or'the alpha substitution products combined with polyhydric alcohol esters of acrylic acid or the alpha substitution products or other polymerizable compound containing more than one independently polymerizable group per molecule.
- EXAMPLE II We mix sixteen hundred and fifty-six grams of suitable abrasive with three hundred and sixtyfive cubic centimeters of monomeric methyl methacrylate, one hundred and twenty-five cubic centimeters of monomeric methacrylic acid, and
- EXAMPLE IV For the manufacture of grinding wheels, we may prefer under some circumstances to produce first a powdered polymer, then, proceed to add the powder to the abrasive grains and mix thoroughly.
- the abrasive may be wet with a suitable liquid before adding the powder.
- a grinding wheel according to this example and procedure may be made of suitable abrasive grains, the powder having been first produced as follows: To one hundred and fifty cubic centimeters of methacrylic acid and four hundred and fifty cubic centimeters of methyl methacrylate is added six-tenths gram of benzoyl peroxide.
- Example- IV we may make a powder from methyl methacrylate, methacrylic .acid and one of the esters containing more than one polymeri zable unsatu-' rated group per molecule.
- esters of alpha chloro acrylic acid may be used within the scope of this invention.
- methyl esterof methacrylic-acid is most commonly referred to, other monohydric alcohol esters,- such as isopropyl, isobutyl or phenyl esters could equally well 'have been While we have described 1 the production of grinding wheel's made from abrasive grains and resin alone, it is .to be understood-that we may the novel resin composition of matter are claimed.
- abrasive grains bonded with a copolymer of compounds comprising methyl methacrylate and methacrylic acid.
- abrasive grains bonded with a copolymer of compounds comprising an acid selected-from the group consisting of acrylic acid and its alpha substitution products in which the substitutent is selected from the group consisting of methyl and chlorine, and a vmonohydric alcohol ester of an acid selected from the-aforesaid group.
Description
Reissued Mar. 4, 1941 .RESIN BONDED ABRASIVE ARTICLE Samuel S. Kistler, West Boylston, and Carl E. Barnes, Worcester, Mass., assignors to Norton Company, Worcester, Mass, a. corporation of Massachusetts No Drawing. Original No. 2,189,734, dated February 6, 1940, Serial No. 187,551, January 28,
1938. Renewed October 31, 1939. Application for reissue September 3, 1940, Serial No. 355,211
2 Claims.
The invention relates to abrasive articles bonded ,with modified polymers of acrylic acid and substituted acrylic acids in which the substituent is either methyl or chlorine and their derivatives.
One object of the invention is to provide an abrasive article bonded with a hard resin of the class indicated. Another object of the invention is to provide an abrasive article bonded with a heat resistant resin of the class indicated, preferably softening above 100 C. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having some of the characteristics of shellacv bonded grinding wheels. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin, having some of the characteristics of rubber. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having characteristics superior to either those of shellac or rubber for certain purposes and capable of substantial duplication in its physical properties. Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having definite characteristics advantageous for the manufacture of grinding wheels.
Another object of the invention is to provide a grinding wheel bonded with a synthetic resin having one or more of the following characteristics: Soft as compared with phenol-formaldehyde, readily controllable, resistant to heat as compared with shellac and rubber, and capable of being made in different degrees of hardness.
Other objects will be in part obvious or in part pointed out hereinafter.
The invention accordingly consists in the combinations of elements and arrangements of parts as will be illustratively described herein, and the scope of the application of which will be indicated in the following claims.
It is known that the esters of acrylic acid and substituted acrylic acids, for example alpha methyl acrylic acid and alpha chloro acrylic acid,
We accordingly propose to copolymerize a suitable ester of acrylic acid or an alpha substituted acrylic acid in which the substituent is either methyl or chlorine with a compatible polymerizable hardening agent comprising acrylic acid. or an alpha substituted acid of the class indicated. We may use the ester and acrylic acidor its alpha substitution products indicated alone or in combination with a third substance containing more than one unsaturated group per molecule, each unsaturated group being capable of independent polymerization. Such substances containing more than one unsaturated group per molecule may be any of the polyhydric alcohol esters of acrylic acid or the indicated alpha substitution products. As examples of the polyhydric alcohols, we mention ethylene glycol, diethylene glycol, triethylene glycol, glycerol, Pentaglycerol, trimethyleneglycol, pentaerythritol, and mannitol. Another suitable substance which contains more than one unsaturated group per molecule is an allyl ester of acrylic or the alpha substituted acrylic acid.
As an example of making a heat resistant resin 25 using methyl methacrylate and methacrylic acid (alpha methyl acrylic acid) we give the following:
EXAMPLE I To seventy-five cubic centimeters of methyl methacrylate and twenty-five cubic centimeters of methacrylic acid, one-hundredth gram of benzoyl peroxide is added. This mixture is heated.
at a temperature of 60 C. for a period of twentyis x TABLE I Tensile strength of resin at 160 C.
Percentage of methacrylic Breaking Tensile acid by volume l Dunne, Area point strength Pounds Lba/i'n.
3. 7 298 4.1 315 4. 1 289 3. 7 303 2. 8 248 3.4 366 3. (i 415 4.9 306 3. 8 392 3.6 410 5. 3 395 5. 416 5.3 395 as 353 5.3 395 6.0 455 6,0 455 6. l 455 5.9 440 6.2 463 Tensile strength of resm at 130 C.
Percentage of methacrylic Diame- Area Breaking Tensile acid by volume ter point strength Pounds Lila/in.
We will now give several examples ofthe manufacture of grinding wheels bonded with the novel resin hereinbefore indicated. A grinding wheel consists of abrasive grain bonded with a given bond which holds the individual grains together in the form of an integral wheel. Other abrasive bodies such as bricks, segments and the like are to be deemed included within the following description and the methods and substances indicated may be used for the manufacture of other abrasive wheels, such as lapping wheels, regulating wheels and the like. For the abrasive we may use any of the usual or known types, such as any yariety of alumina, e. g., fused alumina, emery and corundum, and we may also use silicon carbide or diamonds. Other abrasives such as garnet, quartz, and any of the hard carbides, for example boron carbide or tungsten carbide, might be employed. Among the following examples, we will show how resins may be produced as the copolymers of methyl methacrylate with methacrylic acid and one or more of the esters of methacrylic acid and a'polyhydric alcohol or allyl alcohol, as hereinbefore set forth.
Our novel resin, so far as certain broad aspects are concerned, constitutes on the one hand the copolymerization product of acrylic acid or its alpha substitution products in which the substituent is either methyl or chlorine with monohydric alcohol esters of acrylic acid or the alpha substitution products and, on the other hand, the copolymerization product of acrylic acid or the alpha substitution products with monohydric alcohol esters of acrylic acid or'the alpha substitution products combined with polyhydric alcohol esters of acrylic acid or the alpha substitution products or other polymerizable compound containing more than one independently polymerizable group per molecule.
As examples of the manufacture of grinding wheels according to and illustrating the foregoing, we give the following:
EXAMPLE II We mix sixteen hundred and fifty-six grams of suitable abrasive with three hundred and sixtyfive cubic centimeters of monomeric methyl methacrylate, one hundred and twenty-five cubic centimeters of monomeric methacrylic acid, and
ten cubic centimeters of methyl methacrylate containing one per cent benzoyl peroxide catalyst.
-.The mixture is placed in an aluminum mold consisting of a cylindrical dish having slightly taper-' EXAMPLE III I Proceeding as specified in Example II so far as the various steps including the heat and use of the mold are concerned, we may make .a grinding wheel with sixteen hundred and fifty-six grams of suitable abrasive and the following bond mixture: three hundred and thirty cubic centimeters of methyl methacrylate, one hundred cubic centimeters of methacrylic acid, fifty cubic centimeters of ethylene glycol dimethacrylate, one huntimed and twenty cubic centimeters of methyl methacrylate containing one per cent benzoyl peroxide catalyst.
EXAMPLE IV For the manufacture of grinding wheels, we may prefer under some circumstances to produce first a powdered polymer, then, proceed to add the powder to the abrasive grains and mix thoroughly. The abrasive may be wet with a suitable liquid before adding the powder. A grinding wheel according to this example and procedure may be made of suitable abrasive grains, the powder having been first produced as follows: To one hundred and fifty cubic centimeters of methacrylic acid and four hundred and fifty cubic centimeters of methyl methacrylate is added six-tenths gram of benzoyl peroxide. This mixture is then added to fourteen hundred cubic centimeters of carbon tetrachloride in' which it is completely miscible, and placed in a constant temperature bath maintained at C. After an induction period of about five hours the copolymer, being insoluble in the carbon tetrachloride, begins to precipitate as a fine powder'and'isfiltered off, washed with carbon tetrachloride and dried.
We mix sixteen hundred, and fifty-six grams of abrasive grain with five hundred grams of the above described powder and place in a mold. We press the mixture for thirty minutes in an hydraulic press with platens heated to one hundred and sixty degrees Centigrade, then strip from the mold. The wheel isthen complete, the heat and pressure having softened and coalesced the resin so that it forms with the abrasive grain an integral piece. Y
Proceeding as heretofore outlined in Example- IV, we may make a powder from methyl methacrylate, methacrylic .acid and one of the esters containing more than one polymeri zable unsatu-' rated group per molecule.
In the examples given, we have used only the esters of methacrylic acid. It is tobe understood,
however, that the esters of alpha chloro acrylic acid may be used within the scope of this invention. Also, whereas the methyl esterof methacrylic-acid is most commonly referred to, other monohydric alcohol esters,- such as isopropyl, isobutyl or phenyl esters could equally well 'have been While we have described 1 the production of grinding wheel's made from abrasive grains and resin alone, it is .to be understood-that we may the novel resin composition of matter are claimed.
in separate copending applications Serial Nos. 187,549 and 187,547, filed on January 28, 1938, and in Serial No. 311,934 which is a. continuation of Serial NO. 187,547;
It will thus be seen thatthere has been provided by this invention a composition of matter and article of manufacture in which the various objects hereinabove set forthtogether with many thoroughly practical advantages are successfully achieved. As many possible embodiments may be made of the above invention and as many changes might be made in the embodiments above set forth, it is to be understood that all matter hereinbefore set forth is. to 'be interpreted as illustrative and not in a limiting sense.
We claim:
1. As an article of manufacture, abrasive grains bonded with a copolymer of compounds comprising methyl methacrylate and methacrylic acid.
2. As anarticle of manufacture, abrasive grains bonded with a copolymer of compounds comprising an acid selected-from the group consisting of acrylic acid and its alpha substitution products in which the substitutent is selected from the group consisting of methyl and chlorine, and a vmonohydric alcohol ester of an acid selected from the-aforesaid group.
SAMUEL S. KISTLER.
CARL E. BARNES.
Publications (1)
Publication Number | Publication Date |
---|---|
USRE21737E true USRE21737E (en) | 1941-03-04 |
Family
ID=2087724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US21737D Expired USRE21737E (en) | Resin bonded abrasive article |
Country Status (1)
Country | Link |
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US (1) | USRE21737E (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2426441A (en) * | 1944-01-01 | 1947-08-26 | Dronsfield Samuel Wilkinson | Manufacture of abrasive materials |
US5919603A (en) | 1992-08-28 | 1999-07-06 | Hitachi, Ltd. | Process for producing printed wiring board |
-
0
- US US21737D patent/USRE21737E/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2426441A (en) * | 1944-01-01 | 1947-08-26 | Dronsfield Samuel Wilkinson | Manufacture of abrasive materials |
US5919603A (en) | 1992-08-28 | 1999-07-06 | Hitachi, Ltd. | Process for producing printed wiring board |
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