US2013496A - Abradant - Google Patents
Abradant Download PDFInfo
- Publication number
- US2013496A US2013496A US605113A US60511332A US2013496A US 2013496 A US2013496 A US 2013496A US 605113 A US605113 A US 605113A US 60511332 A US60511332 A US 60511332A US 2013496 A US2013496 A US 2013496A
- Authority
- US
- United States
- Prior art keywords
- acid
- paper
- layer
- condensation product
- abrasive particles
- 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 - Lifetime
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 24
- 239000007859 condensation product Substances 0.000 description 15
- 239000010410 layer Substances 0.000 description 14
- 239000002245 particle Substances 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 13
- 235000011187 glycerol Nutrition 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 9
- 230000001070 adhesive effect Effects 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 8
- 229940106681 chloroacetic acid Drugs 0.000 description 8
- 229910001651 emery Inorganic materials 0.000 description 8
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 229920003002 synthetic resin Polymers 0.000 description 7
- 239000000057 synthetic resin Substances 0.000 description 7
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 230000001427 coherent effect Effects 0.000 description 6
- -1 halogen fatty acid Chemical class 0.000 description 6
- 150000005846 sugar alcohols Polymers 0.000 description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 5
- 229910010271 silicon carbide Inorganic materials 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000003082 abrasive agent Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 150000007519 polyprotic acids Polymers 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 239000008098 formaldehyde solution Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
- 229960003656 ricinoleic acid Drugs 0.000 description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000012237 artificial material Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polishing Bodies And Polishing Tools (AREA)
Description
Patented Sept. 3, 1935 UNITED STATES ABRADANT Georg Krtinzlein,
Frankfort on the Main- Hochst, and Richard Karl Miiller, Bad Sodenon-the-Taunus, Germany, assignors to I. G. Farbenindustrie Aktiengesellschaft, Frankforton-the-Main, Germany No Drawing. Application April 13, 1932, Serial No. 605,113. In Germany October 18, 1930 8 Claims.
The present invention relates to new abradants.
We have found that abradants such as emery paper or whet stones show particularly good properties if they contain as a binding agent a hardened condensation product of a polyhydric alcohol with a mixture of an organic polybasic acid and a fatty acid of at least 10 carbon atoms in the molecule. These condensation products known in the varnish industry as rezyles are mixed esters; they are prepared for instance by esterifying the hydroxyl groups of a polyhydric alcohol in part with a fatty acid and in part with a polyvalent carboxylic acid (see British Patent No. 284,349 and U. S. Patent No. 1,667,189). As polybasic organic acids there may be used for instance: phthalic acid, maleic acid, malonic acid, succinic acid, ether-diglycollic acid of the formula HOOC.CHz.O.CH2.COOH,
furthermore polybasic synthetic resin acids obtainable in known manner by reacting with a halogen fatty acid, particularly with chloroacetic acid upon phenol aldehyde resins, particularly upon phenolformaldehyde resins, being in the A-state; as fatty acids having at least 10 carbon atoms in the molecule there may be used capric acid, laurio acid, palmitic acid, stearic acid, oleic acid, ricinoleic acid. As polyhydric alcohols there may be used for instance glycol, glycerine, polyglycerine, pentaerythrite, mannite -or nitrogen containing polyhydric alcohols such as tri-ethanolamine. As abrasive material there are used all known abrasives that is materials of natural origin such as quartz, sandstone, pumice stone, emery or artificial material such as silicon carbide, electro-corundum or the like. in every desired sizeof grains.
For the preparation of abradants the above mentioned binding agents may be used in form of a solution (dissolved by means of an organic solvent) or in form of an aqueous suspension. As, in contrast to the hitherto used. adhesive substances, thesebinding agents are distinguished by a particularly good adhesive power, there are obtained abradants, for instance, emery papers having an excellent grinding effect and wearing out slowly. Owing to the water-proofing pr perty of the binding agents in question, it is possible to prepare water-proof emery papers in one operation by means of these binding agents. It is unnecessary to add to the binding agents a special additional substance, such as oil, caoutchouc or the like for the purpose of imparting to the abradant the required strength and elasticity.
' of 16 per cent. strength. ened by drying it for 4 hours at C. and for 1 hour at C. In order to further increase the 50 Even if thin paper and a coarse grain abrasive are used the emery papers are very resistant to creasing. I
Instead'of paper there maybe used with the same advantage cloth or paper having, linen threads and the like. Emery papers are made in the usual manner. It may be useful subsequently-to harden the papers at an elevated temperature with or without application of pressure. Furthermore, it may be advantageous to pass the emery papers to which the binding agent and the abrasivehave been applied between rollers which may be heated, thus causing the grains firmly to set in the binding agent.
The adhesive layer may be applied by passing the strips through a bath or by coating the strips, carried on the running band, on one side or on both sides with the adhesive material. The bind- 2o ing agent may be embedded in the paper with the aid of suction and pressure in the manner applied for impregnating wood.
Owing to the extremely high degree ofelasticity of the abradants made according to the present process, it is possible to apply the abrasive on both sides of the paper.
whet-stones can be made by directly moulding the mixture of abrasive material and binding agent so as to form discs which are then hardened. The mixture may also be passed through an extrusion press so as to obtain a more or less thick or broad strip; the discs are then stamped out of this strip and hardened, if desired, by subjecting them simultaneously to heat and pressure.
The following examples serve to illustrate the invention, but they are not intended to limit it thereto:
(1) Glycerine mixed ester from linseed oil and phthalic acid is diluted with twice the quantity 40 by weight of acetone and applied on one side of a strip of paper. The paper strips are passed through a doctor device, then sprinkled with silicon carbide, and rendered smooth by means of a roller. The side which has not been covered 45 with silicon carbide is coated with the same binding agent dissolved in acetone to form a solution The abradant is hardadhesion of the abrasive material, the abradants may be subsequently sized in the usual manner with the same or any other usual binding agent. (2) Glycerine mixed ester from ricinoleic fatty acid and phthalic acid is diluted with methyl- I 55 cyclohexanone until the desired consistency is obtained. A strip of paper is coated on one side with this mixture and then sprinkled with silicon carbide which is pressed into the adhesive layer by application of a slight pressure. After drying the resin has completely and uniformly penetrated the paper; a coating of the other side of the paper can thus be dispensed with. Instead of glycerine there may be used with the same advantage glycol for the preparation of the mixed ester used.
(3) Glycerine mixed ester from linseed oil and phthalic acid is diluted with twice the quantity by weight of acetone and mixed with such a quantity of finely ground silicon powder as will make a suspension which is a very thin liquid lacquer. A band made of asbestos fiber and having a length of 100 cm., a breadth .of cm. and a thickness of 6 mm. is impregnated with this suspension. The band is then dried by exposure to air and dried and hardened for 2 hours at 100 C. and 2 hours at 150 C. to 180 C. The band retains a good elasticity and can be used for abrading purposes and among other applications as a brake band.
(4) A glycerine mixed ester obtained by esterifying in known manner one part of glycerine with 1 part of ricinoleic fatty acid and 2 parts of a synthetic resin acid from cresolformaldehyde and chloroacetic acid. is diluted with methylcyclohex anone in a quantity sufficient to obtain the desired viscosity. This solution is applied on one side of a strip of paper. The paper thus treated is sprinkled with silicon carbide and dried in a drying oven for removing the solvent. The abradants thus prepared can subsequently be coated with the same or any other suitable binding agent.
The above mentioned synthetic resin acid can be prepared by reacting with 60 parts of chloroacetic acid upon the liquid initial condensation product from 100 parts of cresol and 90 parts of a formaldehyde solution of 30% strength.
(5) A glycerine mixed ester obtained by esterifying one part of glycerine with2 parts of linoleic acid and 1 part of a synthetic resin acid from phenolformaldehyde and chloroacetic acid are dissolved in twice the quantity of acetone and applied upon a strip of paper. Afterpassing the paper through a doctor device, they are sprinkled with silicon and rendered smooth by means of a roller.
The rear side of the paper is coated with a 16 per cent. solution of the same binding agent. The abradant is hardened by drying it for 4 hours at 100 C. and for 4 hours at 130 C. The paper can be treated again with the same binding agent.
The synthetic acid in question can be prepared by reacting with 90 parts of chloroacetic acid upon the still soluble and fusible initial condensation product from 90 parts of phenol and 100 parts of a. 30 per cent. formaldehyde solution.
(6) 1 part of a resin consisting of equal parts of the resins'used in Examples 2 and 5 is dissolved in 1 part of acetone and 1 part of methylcyclohexanone. The solution thus obtained is used for preparing emery papers as described in Example 5.
This application contains subject matter in common with our application Serial No. 567,978, filed on October 9, 1931.
We claim:
1. The article of manufacture comprising a grit or layer of abrasive particles and an adhesive bond' for uniting the abrasive particles to form a coherent mass or layer, said bond including a hardened resinous condensation product of a polyhy dric alchohol with a mixture of a polybasic acid from a fusible synthetic resin and a fatty acid of at least 10 carbon atoms.
2. The article of manufacture comprising a grit or layer of abrasive particles and an abrasive bond for uniting the abrasive particles to form a coherent mass or layer, said bond including a harddened resinous condensation product of a polyhydric alcohol with a mixture of a polybasic acid from a fusible synthetic resin and an unsaturated fatty acid of at least 10 carbon atoms.
3. The article of manufacture comprising a grit or layer of abrasive particles and an adhesive bond for uniting the abrasive particles to form a coherent mass or layer, said bond including a hardened condensation product of glycerine with a mixture of a polybasic acid from a fusible synthetic resin and a fatty acid of at least 10 carbon atoms.
4. The article of manufacture comprising a grit or layer of abrasive particles and an adhesive bond. for uniting the abrasive particles to iorm a coherent mass or layer, said bond including a hardened condensation product of a polyhydric alcoformaldehyde condensation product and chloroacetic acid.
6. The article of manufacture comprising a grit or layer of abrasive particles and an adhesive bond for uniting the abrasive particles to form a coherent mass or layer, said bond including a hardened condensation product of glycerine with a mixture of linoleic acid and a polybasic resin acid from a still fusible phenolformaldehyde condensation product and chloroacetic acid.
7. The article of manufacture comprising a grit or layer of abrasive particles and an adhesive bond for uniting the abrasive particles to form a coherentmass or layer, said bond including a hardened condensation product of glycerine with a mixture of ricinoleic acid and a polybasic resin acid from a still fusible phenolformaldehyde condensation product and chloroacetic acid.
8. The article of manufacture comprising a grit or layer of abrasive particles and an adhesive bond for uniting said abrasive particles to form a coherent mass or layer, said bond including a hardened resinous condensation product of a polyhydric alcohol with a mixture of an unsaturated fatty acid of at 'least 10 carbon atoms and a polybasic resin acid from a'still-fusible phenol aldehyde condensation product and a halogen fatty acid.
GEORG RANZL'EIN. RICHARD KARL MULLER.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2013496X | 1930-10-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2013496A true US2013496A (en) | 1935-09-03 |
Family
ID=7965893
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US605113A Expired - Lifetime US2013496A (en) | 1930-10-18 | 1932-04-13 | Abradant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2013496A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2542941A (en) * | 1947-11-04 | 1951-02-20 | Jordan A Post | Wall bracket |
| US2981710A (en) * | 1955-11-22 | 1961-04-25 | Vianova Kunstharz Ag | Water soluble hardenable resinous compositions |
-
1932
- 1932-04-13 US US605113A patent/US2013496A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2542941A (en) * | 1947-11-04 | 1951-02-20 | Jordan A Post | Wall bracket |
| US2981710A (en) * | 1955-11-22 | 1961-04-25 | Vianova Kunstharz Ag | Water soluble hardenable resinous compositions |
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