US2783137A - Grinding compositions and making of same - Google Patents
Grinding compositions and making of same Download PDFInfo
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- US2783137A US2783137A US230693A US23069351A US2783137A US 2783137 A US2783137 A US 2783137A US 230693 A US230693 A US 230693A US 23069351 A US23069351 A US 23069351A US 2783137 A US2783137 A US 2783137A
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- 239000000203 mixture Substances 0.000 title claims description 84
- 238000000227 grinding Methods 0.000 title claims description 63
- 239000002245 particle Substances 0.000 claims description 27
- 239000011347 resin Substances 0.000 claims description 25
- 229920005989 resin Polymers 0.000 claims description 24
- 238000005498 polishing Methods 0.000 claims description 14
- 150000005846 sugar alcohols Polymers 0.000 claims description 14
- 239000000725 suspension Substances 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 11
- 150000001447 alkali salts Chemical class 0.000 claims description 3
- 230000009969 flowable effect Effects 0.000 claims description 3
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 36
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 18
- 239000004793 Polystyrene Substances 0.000 description 17
- 229920002223 polystyrene Polymers 0.000 description 17
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- -1 ar-ethylstyrene Chemical compound 0.000 description 11
- 239000003082 abrasive agent Substances 0.000 description 10
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 10
- 229910000831 Steel Inorganic materials 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- 239000010959 steel Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 125000001931 aliphatic group Chemical group 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- 235000011187 glycerol Nutrition 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 159000000000 sodium salts Chemical class 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000006748 scratching Methods 0.000 description 5
- 230000002393 scratching effect Effects 0.000 description 5
- 230000008719 thickening Effects 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 4
- 229910010271 silicon carbide Inorganic materials 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 3
- 238000009834 vaporization Methods 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- WAEOXIOXMKNFLQ-UHFFFAOYSA-N 1-methyl-4-prop-2-enylbenzene Chemical group CC1=CC=C(CC=C)C=C1 WAEOXIOXMKNFLQ-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 229940093932 potassium hydroxide Drugs 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1454—Abrasive powders, suspensions and pastes for polishing
- C09K3/1463—Aqueous liquid suspensions
Definitions
- compositions provided by the invention are of the type comprising a suspension or dispersion of abrasive particles in a liquid to gelatinous, or grease-like, medium. They are of liquid to gelatinous consistency and are adapted for use in grinding or polishing surfaces of hard, solid materials such as metals, glass, or ceramic materials, etc. For instance, they may be used in grinding valves, glassjoints, or bearings to obtain a tight fit between the complementary parts thereof. They may be applied between surfaces, e. g. of a valve and its seat, which are to be fitted together and the grinding be accomplished by rubbing the composition between such surfaces.
- the grinding maybe done slowly by hand or rapidly in a power driven manner.
- the compositions of the invention differ from conventional grinding compositions as regards the kind of medium in which the abrasive particles are suspended, v p It is well known to admix finely divided abrasives with liquids such as water, mineral lubricating oil, or petroleum jell, etc, and to employ the resultant mixtures, or suspensions, as grinding compositions.
- the eifectiveness of such composition for grinding purposes is dependent to a large extent upon the kind of medium employed and, in part, on the conditions under which the composition is used.
- During use of most such known compositions in grinding operations there is a tendency toward formation of agglomerates of solid particles in the composition which frequently cause scratching or scoring of the surface being ground.
- Such agglomerates are composedeither of abrasive particles coagulated from v the composition, or of particles'ground from the surface of the material under treatment, and in most instances of both such materials. Formation of such agglomerates is usually not of serious consequences when the grinding is performed by hand, since any tendency toward seizure or scoring of the parts being ground may then readily be detected and the grinding composition be removed and replaced with fresh material.
- the known grin-ding compositions comprising suspensions of abrasive particles in liquids, are usually employed in grinding or polishing operations that are to be performed slowly, e. g. by hand; especially when the mate rial .to be gl'oundisfairly soft e. g. .of copper, brass, bronze, nickel, or nick-eLalloy steel, etc.- i
- kenyl aromatic compounds constitute excellent media for use in grinding compositions such as those discussed above. These thickened media have desirable properties of wetting and forming continuous lubricating films over surfaces of solid parts to be ground, of maintaining in dispersed condition both the abrasive particles and particles formed by grinding of the material under treatment, and of rapidly absorbing and dissipating heat generated by the grinding operation.
- the sulphonated alkenyl aromatic resin ingredient appears to perform a number of useful functions, i.
- e thickens and contributes to the lubricating action of the liquid; it reduces the rate of vaporization of the liquid at a given temperature and thus prevents rapid drying of the grinding composition during use; and it serves as a dispersing agent, or a protective colloid, so as to maintain the abrasive particles in suspension and cause dispersion of particles formed firom a material, e. g. a valve, subjected to grinding by the composition.
- a material e. g. a valve
- the sulphonated alkenyl aromatic res-ins which maybe employed as ingredients of the compositions are obtained by the nuclear sulphonati-on of solid polymers and co polymers of monalkenyl aromatic hydrocarbons having the general formula:
- Ar represents an aryl radical and R represents hydrogen or a methyl radical.
- alkenyl aromatic resins are polystyrene, solid polymers of vinyltoluene, vinylxylene, ar-ethylstyrene, alpha-methylstyrene, or ar-methyl-alpha-methylstyrene, etc, and solid .copolymers of such alkenyl aromatic compounds with one another, e. g. copolymers of styrene and alpha-methylstyrene, or of styrene and vinyltoluene, etc.
- any such solid, resinous polymer or copolymer may be sulphonated for use in the compositions of the invention, the polymers and copolymers which, when dissolved in nine times their weight of toluene, form solutions having viscosities of firom 4 to 800 centipoises at 25 C. are most satisfactory.
- Polystyrene is preferably employed.
- the alkenyl aromatic resin is sulphonated in known manner, e. g. using a sulphonat-ing agent such as concentrated or fuming sulphuric acid, chlorosulphonic acid, or sulphur t-riozi-de, etc, to a point at which it'contains an average of from 0.55 to 0.95 sulphonic acid radical per aromatic nucleus.
- a sulphonat-ing agent such as concentrated or fuming sulphuric acid, chlorosulphonic acid, or sulphur t-riozi-de, etc, to a point at which it'contains an average of from 0.55 to 0.95 sulphonic acid radical per aromatic nucleus.
- the mixture is then neutralized by treatment with an alkali such as sodium hydroxide, potas sium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, or ammonia, etc.
- the alkenyl aromatic resin sulphonates thus prepared have a property, when added to water or liquid aliphatic polyhydric alcohols, of dissolving, or-swelling to a sub stantially uniform gel, with resultant increase ii -viscosity of the liquid.
- addition of the resin sulphonates to a monohydric alcohol such as methyl or ethyl alcohol causes relatively little, if any, increase in viscosity of the alcohol.
- the extent to which the viscosity of water or a polyhydric alcohol is increased by addition of such resin sulphonate thereto is dependent upon a number of factors such as the kind of liquid employed, the kind and molecular weight of the alkenyl aromatic resin from which the sulphonate was prepared,gthe extent of sulphonation of such resin, and the proportion of sulphonated resin added to the liquid. Thickening becomes greater as the proportionof an added resin sulphonate is increased.
- an alkenyl aromatic resin sulphonate is added to the water, of aliphatic polyhydric alcohol, in a proportion such that the thickened liquid has a viscosityof from 1,000 to 50,000,preferably from 5,000 to 40,000, I
- any liquid saturated aliphatic polyhydric alcohol may be used in the compositions, but those containing not more than six carbon atoms and having an average of three or less carbon atoms per hydroxyl group in the molecule are preferred.
- abrasive material in the form of fine grains or particles, is added to the liquid thus thickened with the alkenyl aromatic resin sulphonate and the mixture is stirred to form a suspension of the abrasive particles in the liquid.
- Any of the usual abrasives such as silicon carbide, aluminum oxide, silicon dioxide, ferric oxide, or powdered glass, etc., may be used in the composition.
- the abrasive is usually in the form of particles or granules of between 100 and 360 mesh size on the Tyler standard screen scale, but smaller or larger particles can be used.
- the choices as to kind and grain size of abrasive to be employed are dependent in part on the kind of material to be ground and the fineness of grinding desired.
- the abrasive should be a material harder than that to be ground, but where polishing is the principal objective, the abrasive may be as soft, or softer, than the material to be polished. In general, the coarseness of grinding increases with increase in size of the abrasive particles in the composition.
- the proportion of abrasive material added in forming the composition may be varied widely, e. g. from that forming a mobile, or flownble, composition to that forming a fairly stiff, non-flowable paste.
- the composition should contain sufficient liquid to serve as a medium in which the abrasive particles are suspended.
- the abrasive is added in amount corresponding to from 0.5 to 50, preferably from to 30, percent of the weight of the composition, but it may be employed in smaller or larger proportions.
- compositions prepared as just described are suitable for direct employment as grinding or polishing compositions.
- other usual ingredients such as dyes,
- pigments, waxes, perfumes, or essential oils, etc. may be added, if desired, to give such composition a pleasing appearance, or fragrance, or to otherwise modify .its properties.
- compositions prepared in accordance with the invention are suitable for the grinding or polishing of corrosion-resistant materials such as glass, or stainless steel, etc.
- the compositions comprising water as the liquid vehicle cause rusting of iron or steel if retained thereon, whereas those containing a polyhydric alcohol as the liquid vehicle do not have appreciable effect in accelerating the rusting of iron or steel.
- the polyhydric alcohols in the latter compositions need not be entirely anhydrous, e. g. the alcohol ingredient may contain up to about 10 percent by weight of water without greatly accelerating rusting of iron or steel contacted with the compositions.
- compositions comprising polyhydric alcohols of 90 percent concentration or higher constitute a preferred embodiment of the invention.
- compositions may be employed in ways customary with other grinding and polishing compositions, e. g. where polishing is desired they may be applied and rubbed over a surface with a cloth, or a butiing wheel, etc.
- polishing For purpose of grinding valves, or joints of glass or a metal, they are usually applied between surfaces of the parts which are to be fitted by grinding and the parts are rotated or oscillated while being pressed together. It is an advantage of the compositions of the invention that they permit grinding at high speeds in a motor driven manner without excessive danger of irregularly scratching or scoring the surfaces being ground.
- the alkenyl aromatic resin sulphonate ingredient of the composition causes rapid dispersement, throughout the liquid vehicle, of particles formed by the grinding and thus prevents formation of solid agglomerates of the particles such as would cause scratching.
- the thickened liquid vehicle also serves as a lubricant to prevent binding of the parts being ground.
- Example 1 Approximately 2 parts by weight of a sodium salt of sulphonated polystyrene was admixed with 98 parts of water to form a substantially uniform, viscous liquid medium.
- the sulphonated polystyrene salt contained an average of about 0.7 of a sulphonate radical per benzene nucleus thereof. It was prepared from ordinary polystyrene of a molding quality, i. e. from solid polystyrene having a molecular weight of between 75,000 and 150,000 as determined by the well known Staudinger viscosity method.
- the sodium polystyrene sulphonate appeared to dissolve when admixed with the water, presumably with formation of a colloidal solution of the sulphonate.
- the solution had a viscosity of 378 centistokes at 25 C.
- the resultant composition was applied to the contacting surfaces of a roughly formed glass joint and was used in grinding the joint to obtain a tight fit. It was found to be highly satisfactory for the purpose and did not cause scratching or scoring of the parts being ground. The experiment was repeated in grinding other glass joints.
- Example 2 To 98 parts by weight of an aqueous glycerine solution, containing 10 percent by weight of glycerine, there was added 2 parts of a sodium salt of sulphonated polystyrene.
- the sulphonated polystyrene salt was obtained by sulphonating polystyrene to a stage at which it contained an average of approximately 0.7 sulphonic acid radical per aromatic nucleus, neutralizing the sulphonated polystyrene to form a sodium salt thereof, and separating the salt as a substantially dry powder.
- Example 3 A grinding composition was prepared and tested, as in Example 2, except that the liquid medium in the composition was an aqueous glycerine solution containing 50 percent by weight of glycerine. During grinding of a steel plug cock with this composition, the latter did not thicken greatly, i. e. the grinding did not cause a pronounced loss of the liquid medium by vaporization. The composition proved satisfactory from a viewpoint of effecting a uniform grinding without scoring of the parts being ground. Also, the composition was readily wiped from the ground parts to leave the latter apparently clean. However, the ground plug cock parts were permitted to stand While coated with the grinding composition for purpose of determining whether the latter would cause rusting. After one day of standing, the parts were noticeably rusted, but the rusting was not as extensive as that reported in Example 2.
- Example 4 Approximately 98 parts by weight of propylene glycol was thickened with 2 parts of a sodium salt of sulphonated polystyrene. The latter contained an average of about 0.7 sulphonate radical per aromatic nucleus.
- the polystyrene from which the salt was derived was of a molecular weight such that a percent by weight solution thereof in toluene had a viscosity of centistokes at 25 C.
- the mixture was stirred to form a suspension of the particles in the thickened propylene glycol and the resultant composition was employed to grind steel plug cocks at a rapid rate with power driving of the parts being ground.
- the grinding operations were carried out without seizure or scoring of the parts being ground and without noticeable thickening of, or loss of liquid from, the grinding composition used.
- the ground parts fitted well. After completing the grinding operations, the composition was readily wiped from the ground parts to leave the latter apparently clean.
- the ground parts of a steel plug cock were permitted to stand, under ordinary room conditions, while coated with the grinding composition to determine whether rusting would occur.
- the plug cock parts were not rusted after 48 hours of standing under the conditions just stated. Accordingly, the grinding composition of this example is suitable for the grinding of iron or steel parts.
- composition, as claimed in claim 1, wherein the salt of the sulphonated alkenyl aromatic resin is one containing an average of from 0.55 to 0.95 sulphonate radical per aromatic nucleus thereof.
- composition, as claimed in claim 2, wherein the salt of the sulphonated alkenyl aromatic resin is an alkali metal salt of sulphonated polystyrene.
- a method of making grinding and polishing compositions which comprises, as the essential steps thereof, thickening a liquid of the group consisting of water, aliphatic polyhydric alcohols, and mixtures thereof, by adding to the same a minor amount of an alkali salt of a sulphonated alkenyl aromatic resin, thereafter adding to the thickened liquid a finely divided abrasive material,
- a method, as claimed in claim 4, wherein the salt of the sulphonated alkenyl aromatic resin is one con taining an average of from 0.55 to 0.95 sulphonate radical per aromatic nucleus thereof.
- a method, as claimed in claim 5, wherein the salt of the sulphonated alkenyl aromatic resin is an alkali metal salt of sulphonated polystyrene.
- a composition adapted for use in grinding and polishing operations, consisting essentially of a suspension of solid abrasive particles in a fiowable medium consisting essentially of at least one aliphatic polyhydric alcohol, containing not more than six carbon atoms and having an average of not more than three carbon atoms per hydroxyl group in the molecule, thickened with a small amount of an alkali metal salt of a sulfonated alkenyl aromatic resin.
- a composition adapted for use in grinding and polishing operations, consisting essentially of a suspension of solid abrasive particles in a flowable medium consisting essentially of propylene glycol thickened with a small amount of a sodium salt of sulfonated polystryrene.
- a method of making grinding and polishing compositions which comprises, as the essential steps thereof, thickening a liquid consisting essentially of at least one aliphatic polyhydric alcohol, containing not more than six carbon atoms and having an average of not more than three carbon atoms per hydroxyl group in the molecule, by adding to the liquid a minor amount of an alkali salt of a sulfonated alkenyl aromatic resin, thereafter adding to the thickened liquid a finely divided abrasive material, and agitating the mixture to form a suspension of the abrasive material in the thickened liquid.
- a method of making grinding and polishing compositions which comprises, as the essential steps thereof, thickening propylene glycol by adding thereto a minor amount of a sodium salt of sulfonated polystyrene, thereafter adding to the thickened liquid a finely divided abrasive material, and agitating the mixture to form a suspension of the abrasive material in the thickened liquid.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
Description
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United States Patent GRINDING COMPOSITIONS AND MAKING OF SAME NoDrawing. Application June 8 .1951, Serial N0. 230,693
10 Claims. (Cl. 51-402) This invention concerns certain new grinding compositions and a method of making the same -The compositions provided by the invention are of the type comprising a suspension or dispersion of abrasive particles in a liquid to gelatinous, or grease-like, medium. They are of liquid to gelatinous consistency and are adapted for use in grinding or polishing surfaces of hard, solid materials such as metals, glass, or ceramic materials, etc. For instance, they may be used in grinding valves, glassjoints, or bearings to obtain a tight fit between the complementary parts thereof. They may be applied between surfaces, e. g. of a valve and its seat, which are to be fitted together and the grinding be accomplished by rubbing the composition between such surfaces. The grinding maybe done slowly by hand or rapidly in a power driven manner. The compositions of the invention differ from conventional grinding compositions as regards the kind of medium in which the abrasive particles are suspended, v p It is well known to admix finely divided abrasives with liquids such as water, mineral lubricating oil, or petroleum jell, etc, and to employ the resultant mixtures, or suspensions, as grinding compositions. The eifectiveness of such composition for grinding purposes is dependent to a large extent upon the kind of medium employed and, in part, on the conditions under which the composition is used. During use of most such known compositions in grinding operations there is a tendency toward formation of agglomerates of solid particles in the composition which frequently cause scratching or scoring of the surface being ground. Such agglomerates are composedeither of abrasive particles coagulated from v the composition, or of particles'ground from the surface of the material under treatment, and in most instances of both such materials. Formation of such agglomerates is usually not of serious consequences when the grinding is performed by hand, since any tendency toward seizure or scoring of the parts being ground may then readily be detected and the grinding composition be removed and replaced with fresh material. However, heat generated in a rapid powerdriven grinding operation appears to induce formation of agglomerates and the tendency toward seizure during such operation cannot readily be detected until the parts being ground have been severely scratched or scored; For these reasons, the known grin-ding compositions, comprising suspensions of abrasive particles in liquids, are usually employed in grinding or polishing operations that are to be performed slowly, e. g. by hand; especially when the mate rial .to be gl'oundisfairly soft e. g. .of copper, brass, bronze, nickel, or nick-eLalloy steel, etc.- i
it isan object of this invention toiprovide certain new grinding compositions which are adapted for use either in hand grinding or polishing operations, or where the parts to be ground are-powerdriven. Other andrelated objects will be evident from the following description of the invention.
,, 'lihavej-found that polyhydric ened by addition of salts of 'sulphonatcd'polymers 'of a1- all) "ice
kenyl aromatic compounds, constitute excellent media for use in grinding compositions such as those discussed above. These thickened media have desirable properties of wetting and forming continuous lubricating films over surfaces of solid parts to be ground, of maintaining in dispersed condition both the abrasive particles and particles formed by grinding of the material under treatment, and of rapidly absorbing and dissipating heat generated by the grinding operation. The sulphonated alkenyl aromatic resin ingredient appears to perform a number of useful functions, i. e, it thickens and contributes to the lubricating action of the liquid; it reduces the rate of vaporization of the liquid at a given temperature and thus prevents rapid drying of the grinding composition during use; and it serves asa dispersing agent, or a protective colloid, so as to maintain the abrasive particles in suspension and cause dispersion of particles formed firom a material, e. g. a valve, subjected to grinding by the composition. I
The sulphonated alkenyl aromatic res-ins which maybe employed as ingredients of the compositions are obtained by the nuclear sulphonati-on of solid polymers and co polymers of monalkenyl aromatic hydrocarbons having the general formula:
wherein Ar represents an aryl radical and R represents hydrogen or a methyl radical. Examples of such alkenyl aromatic resins are polystyrene, solid polymers of vinyltoluene, vinylxylene, ar-ethylstyrene, alpha-methylstyrene, or ar-methyl-alpha-methylstyrene, etc, and solid .copolymers of such alkenyl aromatic compounds with one another, e. g. copolymers of styrene and alpha-methylstyrene, or of styrene and vinyltoluene, etc. Although any such solid, resinous polymer or copolymer may be sulphonated for use in the compositions of the invention, the polymers and copolymers which, when dissolved in nine times their weight of toluene, form solutions having viscosities of firom 4 to 800 centipoises at 25 C. are most satisfactory. Polystyrene is preferably employed.
The alkenyl aromatic resin is sulphonated in known manner, e. g. using a sulphonat-ing agent such as concentrated or fuming sulphuric acid, chlorosulphonic acid, or sulphur t-riozi-de, etc, to a point at which it'contains an average of from 0.55 to 0.95 sulphonic acid radical per aromatic nucleus. The mixture is then neutralized by treatment with an alkali such as sodium hydroxide, potas sium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, or ammonia, etc. The resultant alkenyl aromatic resin sulphonate is separated, preferably in dry form. Procedures for carrying out these operations are known in the art.
The alkenyl aromatic resin sulphonates thus prepared have a property, when added to water or liquid aliphatic polyhydric alcohols, of dissolving, or-swelling to a sub stantially uniform gel, with resultant increase ii -viscosity of the liquid. Peculiarly, addition of the resin sulphonates to a monohydric alcohol such as methyl or ethyl alcohol causes relatively little, if any, increase in viscosity of the alcohol. The extent to which the viscosity of water or a polyhydric alcohol is increased by addition of such resin sulphonate thereto is dependent upon a number of factors such as the kind of liquid employed, the kind and molecular weight of the alkenyl aromatic resin from which the sulphonate was prepared,gthe extent of sulphonation of such resin, and the proportion of sulphonated resin added to the liquid. Thickening becomes greater as the proportionof an added resin sulphonate is increased. For the purpose of this inventiom an alkenyl aromatic resin sulphonate is added to the water, of aliphatic polyhydric alcohol, in a proportion such that the thickened liquid has a viscosityof from 1,000 to 50,000,preferably from 5,000 to 40,000, I
centistokes at 25 C.
Examples of aliphatic polyhydric alcohols which may be thickened with alkenyl aromatic resin sulphonates and be employed in the compositions of the invention are ethylene glycol, propylene glycol, butylene glycol, glycerine, diethylene glycol, and dipropylene glycol, etc. Apparently, any liquid saturated aliphatic polyhydric alcohol may be used in the compositions, but those containing not more than six carbon atoms and having an average of three or less carbon atoms per hydroxyl group in the molecule are preferred.
An abrasive material, in the form of fine grains or particles, is added to the liquid thus thickened with the alkenyl aromatic resin sulphonate and the mixture is stirred to form a suspension of the abrasive particles in the liquid. Any of the usual abrasives, such as silicon carbide, aluminum oxide, silicon dioxide, ferric oxide, or powdered glass, etc., may be used in the composition. The abrasive is usually in the form of particles or granules of between 100 and 360 mesh size on the Tyler standard screen scale, but smaller or larger particles can be used. The choices as to kind and grain size of abrasive to be employed are dependent in part on the kind of material to be ground and the fineness of grinding desired. Where considerable cutting away of material is desired during grinding, the abrasive should be a material harder than that to be ground, but where polishing is the principal objective, the abrasive may be as soft, or softer, than the material to be polished. In general, the coarseness of grinding increases with increase in size of the abrasive particles in the composition.
The proportion of abrasive material added in forming the composition may be varied widely, e. g. from that forming a mobile, or flownble, composition to that forming a fairly stiff, non-flowable paste. The composition should contain sufficient liquid to serve as a medium in which the abrasive particles are suspended. In most instances, the abrasive is added in amount corresponding to from 0.5 to 50, preferably from to 30, percent of the weight of the composition, but it may be employed in smaller or larger proportions.
The compositions prepared as just described are suitable for direct employment as grinding or polishing compositions. However, other usual ingredients such as dyes,
pigments, waxes, perfumes, or essential oils, etc., may be added, if desired, to give such composition a pleasing appearance, or fragrance, or to otherwise modify .its properties.
All of the compositions prepared in accordance with the invention are suitable for the grinding or polishing of corrosion-resistant materials such as glass, or stainless steel, etc. However, the compositions comprising water as the liquid vehicle cause rusting of iron or steel if retained thereon, whereas those containing a polyhydric alcohol as the liquid vehicle do not have appreciable effect in accelerating the rusting of iron or steel. The polyhydric alcohols in the latter compositions need not be entirely anhydrous, e. g. the alcohol ingredient may contain up to about 10 percent by weight of water without greatly accelerating rusting of iron or steel contacted with the compositions. In instances in which corrosive-resistant materials are to be ground, mixtures of water with one or more of the polyhydric alcohols in any desired proportions may be used as vehicles for the compositions. The polyhydric alcohols of 90 percent concentration or higher, preferably anhydrous, possess a further advantage of being far less volatile, i. e. of higher boiling point, than water so that the compositions containing them as vehicles have less tendency to undergo drying during use, and may be employed at higher temperatures, than the compositions containing water as the vehicle. For these reasons, the compositions comprising polyhydric alcohols of 90 percent concentration or higher constitute a preferred embodiment of the invention.
The compositions may be employed in ways customary with other grinding and polishing compositions, e. g. where polishing is desired they may be applied and rubbed over a surface with a cloth, or a butiing wheel, etc. For purpose of grinding valves, or joints of glass or a metal, they are usually applied between surfaces of the parts which are to be fitted by grinding and the parts are rotated or oscillated while being pressed together. It is an advantage of the compositions of the invention that they permit grinding at high speeds in a motor driven manner without excessive danger of irregularly scratching or scoring the surfaces being ground. Apparently, the alkenyl aromatic resin sulphonate ingredient of the composition causes rapid dispersement, throughout the liquid vehicle, of particles formed by the grinding and thus prevents formation of solid agglomerates of the particles such as would cause scratching. The thickened liquid vehicle also serves as a lubricant to prevent binding of the parts being ground.
The following examples describe a number of ways in which the invention has been applied and illustrate certain of its advantages, but are not to be construed as limiting the invention.
Example 1 Approximately 2 parts by weight of a sodium salt of sulphonated polystyrene was admixed with 98 parts of water to form a substantially uniform, viscous liquid medium. The sulphonated polystyrene salt contained an average of about 0.7 of a sulphonate radical per benzene nucleus thereof. It was prepared from ordinary polystyrene of a molding quality, i. e. from solid polystyrene having a molecular weight of between 75,000 and 150,000 as determined by the well known Staudinger viscosity method. The sodium polystyrene sulphonate appeared to dissolve when admixed with the water, presumably with formation of a colloidal solution of the sulphonate. The solution had a viscosity of 378 centistokes at 25 C. Approximately 30 parts by weight of finely divided silicon carbide, in the form of particles of from to 200 mesh size, was added to the solution and the mixture was stirred to form a suspension of the particles in the thickened liquid. The resultant composition was applied to the contacting surfaces of a roughly formed glass joint and was used in grinding the joint to obtain a tight fit. It was found to be highly satisfactory for the purpose and did not cause scratching or scoring of the parts being ground. The experiment was repeated in grinding other glass joints. Certain of the grinding operations were carried out by hand and others were carried out at high speed using a motor to turn the parts being ground. In all instances, the grinding was accomplished satisfactorily without seizure, scoring, or other damage to the parts being ground. It was observed that the grinding composition adheres well to the parts being ground and that the grinding could be accomplished while holding the surfaces under treatment in either vertical, or horizontal, positions, i. e. the composition did not flow away from the surfaces under treatment. The composition was also applied satisfactorily in grinding glass to form spherical balls of from A inch to 4: inch diameter.
Example 2 To 98 parts by weight of an aqueous glycerine solution, containing 10 percent by weight of glycerine, there was added 2 parts of a sodium salt of sulphonated polystyrene. The sulphonated polystyrene salt was obtained by sulphonating polystyrene to a stage at which it contained an average of approximately 0.7 sulphonic acid radical per aromatic nucleus, neutralizing the sulphonated polystyrene to form a sodium salt thereof, and separating the salt as a substantially dry powder. On adding anddissolving the sodium polystyrene sulphonate in the aqueous glycerine,--the viscosity of the liquid; increased greatly. To'73'partsby weight of the thickened aqueous glycerine solution there wasadded 27 parts of silicon carbide in the form of particles of from 250 to 329 mesh size. The mixture was stirred to form a suspension of the particles in the liquid and the resultant composition was applied to the plug of a steel plug cock and used in grinding the plug and its seat to obtain a close fit. The grinding was accomplished by rapid twisting, with a motor, of the plug in its seat. The grinding occurred satisfactorily without uneven scratching or scoring of the parts. However, it was noted that the grinding composition thickened materially, during the grinding operation, due to vaporization of a portion of the liquid medium therefrom. The residual composition adhered tightly to the ground plug cock parts, i. e. it was difiicult to wipe all traces of the composition from the parts with a cloth. It was noted that the ground plug cock parts became rusted after standing in the room for a day. Apparently, traces of the grinding composition which were retained on the parts promoted rusting of the latter.
Example 3 A grinding composition was prepared and tested, as in Example 2, except that the liquid medium in the composition was an aqueous glycerine solution containing 50 percent by weight of glycerine. During grinding of a steel plug cock with this composition, the latter did not thicken greatly, i. e. the grinding did not cause a pronounced loss of the liquid medium by vaporization. The composition proved satisfactory from a viewpoint of effecting a uniform grinding without scoring of the parts being ground. Also, the composition was readily wiped from the ground parts to leave the latter apparently clean. However, the ground plug cock parts were permitted to stand While coated with the grinding composition for purpose of determining whether the latter would cause rusting. After one day of standing, the parts were noticeably rusted, but the rusting was not as extensive as that reported in Example 2.
Example 4 Approximately 98 parts by weight of propylene glycol was thickened with 2 parts of a sodium salt of sulphonated polystyrene. The latter contained an average of about 0.7 sulphonate radical per aromatic nucleus. The polystyrene from which the salt was derived was of a molecular weight such that a percent by weight solution thereof in toluene had a viscosity of centistokes at 25 C. To 70 parts by weight of the solution of the sodium salt of sulphonated polystyrene in the propylene glycol there was added 30 parts of silicon carbide in the form of particles of from 250 to 320 mesh size. The mixture was stirred to form a suspension of the particles in the thickened propylene glycol and the resultant composition was employed to grind steel plug cocks at a rapid rate with power driving of the parts being ground. The grinding operations were carried out without seizure or scoring of the parts being ground and without noticeable thickening of, or loss of liquid from, the grinding composition used. The ground parts fitted well. After completing the grinding operations, the composition was readily wiped from the ground parts to leave the latter apparently clean. However, the ground parts of a steel plug cock were permitted to stand, under ordinary room conditions, while coated with the grinding composition to determine whether rusting would occur. The plug cock parts were not rusted after 48 hours of standing under the conditions just stated. Accordingly, the grinding composition of this example is suitable for the grinding of iron or steel parts.
Other modes of applying the principle of the invention may be employed instead of those explained, change being made as regards the method or compositions herein disclosed, provided the steps or ingredients stated by any of the following claims or the equivalent of such stated 7 steps or ingredients be employed.
r a sulphonated alkenyl aromatic resin.
2. A composition, as claimed in claim 1, wherein the salt of the sulphonated alkenyl aromatic resin is one containing an average of from 0.55 to 0.95 sulphonate radical per aromatic nucleus thereof.
3. A composition, as claimed in claim 2, wherein the salt of the sulphonated alkenyl aromatic resin is an alkali metal salt of sulphonated polystyrene.
4. A method of making grinding and polishing compositions which comprises, as the essential steps thereof, thickening a liquid of the group consisting of water, aliphatic polyhydric alcohols, and mixtures thereof, by adding to the same a minor amount of an alkali salt of a sulphonated alkenyl aromatic resin, thereafter adding to the thickened liquid a finely divided abrasive material,
and agitating the mixture to form a suspension of the abrasive material in the thickened liquid.
5. A method, as claimed in claim 4, wherein the salt of the sulphonated alkenyl aromatic resin is one con taining an average of from 0.55 to 0.95 sulphonate radical per aromatic nucleus thereof.
6. A method, as claimed in claim 5, wherein the salt of the sulphonated alkenyl aromatic resin is an alkali metal salt of sulphonated polystyrene.
7. A composition, adapted for use in grinding and polishing operations, consisting essentially of a suspension of solid abrasive particles in a fiowable medium consisting essentially of at least one aliphatic polyhydric alcohol, containing not more than six carbon atoms and having an average of not more than three carbon atoms per hydroxyl group in the molecule, thickened with a small amount of an alkali metal salt of a sulfonated alkenyl aromatic resin.
8. A composition, adapted for use in grinding and polishing operations, consisting essentially of a suspension of solid abrasive particles in a flowable medium consisting essentially of propylene glycol thickened with a small amount of a sodium salt of sulfonated polystryrene.
9. A method of making grinding and polishing compositions which comprises, as the essential steps thereof, thickening a liquid consisting essentially of at least one aliphatic polyhydric alcohol, containing not more than six carbon atoms and having an average of not more than three carbon atoms per hydroxyl group in the molecule, by adding to the liquid a minor amount of an alkali salt of a sulfonated alkenyl aromatic resin, thereafter adding to the thickened liquid a finely divided abrasive material, and agitating the mixture to form a suspension of the abrasive material in the thickened liquid.
10. A method of making grinding and polishing compositions which comprises, as the essential steps thereof, thickening propylene glycol by adding thereto a minor amount of a sodium salt of sulfonated polystyrene, thereafter adding to the thickened liquid a finely divided abrasive material, and agitating the mixture to form a suspension of the abrasive material in the thickened liquid.
References Cited in the file of this patent UNITED STATES PATENTS Holmes Jan. 7, 1921 Glenning May 31, 1938 UNITED STATES PATENTS Brown Iunc 1.8, 11940 Kistler 1- Nov. 26, 1940 Dec. 21, 1950 Roth July 22, 1952 Bear et a1. Sept. 30, 1952 8 FOREIGN PATENTS Germany July 13, 1933 Italy Aug. 27, 1948 Great Britain Aug. 30, 1928
Claims (1)
1. A COMPOSITION, ADAPTD FOR USE IN GRINDING AND POLISHING OPERATIONS, CONSISTING ESSENTIALLY OF A SUSPENSION OF SOLID ABRASIVE PARTICLES IN A FLOWABLE MEDIUM CONSISTING ESSENTIALLY OF A LIQUED, OF THE GROUP CONSISTING OF WATER, ALIPHATIC POLYHYDRIC ALCOHOLS, AND MIXTURES THEREOF, THICKENED WITH A SMALL AMOUNT OF AN ALKALI SALT OF A SULPHONATED ALKENYL AROMATIC RESIN.
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US230693A US2783137A (en) | 1951-06-08 | 1951-06-08 | Grinding compositions and making of same |
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US230693A US2783137A (en) | 1951-06-08 | 1951-06-08 | Grinding compositions and making of same |
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US2783137A true US2783137A (en) | 1957-02-26 |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3020140A (en) * | 1959-01-19 | 1962-02-06 | John M Bluth | Compositions for metal surface reformation |
US3053646A (en) * | 1960-07-15 | 1962-09-11 | Dow Chemical Co | Grinding and polishing compositions and method of making same |
US3607350A (en) * | 1967-12-05 | 1971-09-21 | Dow Chemical Co | Electroless plating of plastics |
FR2176798A1 (en) * | 1972-03-17 | 1973-11-02 | Union Carbide Corp | |
US4038048A (en) * | 1975-02-14 | 1977-07-26 | Thrower Jr Herbert T | Lapping composition containing a carboxy vinyl polymer |
US4126277A (en) * | 1976-05-19 | 1978-11-21 | The Dow Chemical Company | Process for grinding coal or ores in a liquid medium |
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US1380382A (en) * | 1920-09-27 | 1921-06-07 | Harold S Holmes | Grinding compound |
GB296195A (en) * | 1927-08-30 | 1928-08-30 | Henry Robert Power Chemist | Improvements in abrasive compositions |
DE580366C (en) * | 1930-09-05 | 1933-07-13 | I G Farbenindustrie Akt Ges | Process for the preparation of sulfuric acid derivatives of polymeric compounds |
US2119159A (en) * | 1937-01-21 | 1938-05-31 | Du Pont | Buffing compositions |
US2205115A (en) * | 1937-04-27 | 1940-06-18 | Standard Oil Dev Co | Silver polish |
US2222969A (en) * | 1938-01-05 | 1940-11-26 | Monsanto Chemicals | Buffing and polishing composition |
US2533211A (en) * | 1950-12-12 | Process for stjlfonating | ||
US2604461A (en) * | 1950-07-22 | 1952-07-22 | Dow Chemical Co | Production of sulfonated alkenyl aromatic resins |
US2612485A (en) * | 1949-08-11 | 1952-09-30 | Monsanto Chemicals | Aqueous dispersions containing a water-soluble sulfonated polystyrene |
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1951
- 1951-06-08 US US230693A patent/US2783137A/en not_active Expired - Lifetime
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2533211A (en) * | 1950-12-12 | Process for stjlfonating | ||
US1380382A (en) * | 1920-09-27 | 1921-06-07 | Harold S Holmes | Grinding compound |
GB296195A (en) * | 1927-08-30 | 1928-08-30 | Henry Robert Power Chemist | Improvements in abrasive compositions |
DE580366C (en) * | 1930-09-05 | 1933-07-13 | I G Farbenindustrie Akt Ges | Process for the preparation of sulfuric acid derivatives of polymeric compounds |
US2119159A (en) * | 1937-01-21 | 1938-05-31 | Du Pont | Buffing compositions |
US2205115A (en) * | 1937-04-27 | 1940-06-18 | Standard Oil Dev Co | Silver polish |
US2222969A (en) * | 1938-01-05 | 1940-11-26 | Monsanto Chemicals | Buffing and polishing composition |
US2612485A (en) * | 1949-08-11 | 1952-09-30 | Monsanto Chemicals | Aqueous dispersions containing a water-soluble sulfonated polystyrene |
US2604461A (en) * | 1950-07-22 | 1952-07-22 | Dow Chemical Co | Production of sulfonated alkenyl aromatic resins |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3020140A (en) * | 1959-01-19 | 1962-02-06 | John M Bluth | Compositions for metal surface reformation |
US3053646A (en) * | 1960-07-15 | 1962-09-11 | Dow Chemical Co | Grinding and polishing compositions and method of making same |
US3607350A (en) * | 1967-12-05 | 1971-09-21 | Dow Chemical Co | Electroless plating of plastics |
FR2176798A1 (en) * | 1972-03-17 | 1973-11-02 | Union Carbide Corp | |
US4038048A (en) * | 1975-02-14 | 1977-07-26 | Thrower Jr Herbert T | Lapping composition containing a carboxy vinyl polymer |
US4126277A (en) * | 1976-05-19 | 1978-11-21 | The Dow Chemical Company | Process for grinding coal or ores in a liquid medium |
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