EP0536596B1 - Schleifmittel - Google Patents

Schleifmittel Download PDF

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Publication number
EP0536596B1
EP0536596B1 EP92116325A EP92116325A EP0536596B1 EP 0536596 B1 EP0536596 B1 EP 0536596B1 EP 92116325 A EP92116325 A EP 92116325A EP 92116325 A EP92116325 A EP 92116325A EP 0536596 B1 EP0536596 B1 EP 0536596B1
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EP
European Patent Office
Prior art keywords
weight
monomers
binder
carbon atoms
acid
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Expired - Lifetime
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EP92116325A
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German (de)
English (en)
French (fr)
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EP0536596A1 (de
Inventor
Thomas Dr. Schwerzel
Kurt Dr. Wendel
Hermann Rockstroh
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BASF SE
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BASF SE
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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B24—GRINDING; POLISHING
    • B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/20—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic

Definitions

  • the present invention relates to abrasives based on finely divided abrasive particles bonded to one another and / or on a carrier, the binder being the solids content of an aqueous polymer dispersion which can be obtained by free-radically polymerizable unsaturated monomers in the presence of an aqueous phase
  • Monosaccharides, oligosaccharides, polysaccharides, oxidatively, hydrolytically and / or enzymatically degraded polysaccharides, chemically modified mono-, oligo- or polysaccharides or mixtures of the compounds mentioned are polymerized by the process of free-radical aqueous emulsion polymerization.
  • abrasives are known whose abrasive particles are bonded with a radiation-curable polymeric binder to achieve satisfactory properties.
  • the disadvantage of radiation curing is disadvantageous.
  • the object of the present invention was therefore to provide fully satisfactory abrasives based on polymeric binders which do not require radiation curing. Accordingly, the abrasives defined at the outset were found.
  • abrasive particles fused or sintered corundum, zirconium corundum, silicon carbide and emery.
  • Flexible substrates such as e.g. Paper, vulcanized fiber, woven fabrics, knitted fabrics, nonwovens based on natural and / or synthetic fibers, plastic films or metal foils.
  • Radically polymerizable monomers include, in particular, monoethylenically unsaturated monomers such as olefins, for example ethylene, vinylaromatic monomers such as styrene, ⁇ -methylstyrene, o-chlorostyrene or vinyltoluenes, vinyl and vinylidene halides such as vinyl and vinylidene chloride, esters of vinyl alcohol and 1 to 18 C Monocarboxylic acids containing atoms, such as vinyl acetate, vinyl propionate, vinyl n-butyrate, Vinyl laurate and vinyl stearate, esters of preferably 3 to 6 carbon atoms have ⁇ , ⁇ -monoethylenically unsaturated mono- and dicarboxylic acids, such as in particular acrylic acid, methacrylic acid, maleic acid, fumaric acid and itaconic acid, with generally 1 to 12, preferably 1 to 8 and in particular Alkanols containing 1 to 4 carbon atoms, such as,
  • the monomers mentioned are essentially insoluble in an aqueous medium and generally form the main monomers which, based on the total amount of the monomers to be polymerized, normally account for more than 50% by weight.
  • Monomers which, when polymerized on their own, usually give homopolymers which have an increased solubility in water, are normally only used as modifying monomers in amounts, based on the total amount of the monomers to be polymerized, of less than 50% by weight, generally 0.5 up to 20, preferably 1 to 10 wt .-%, co-polymerized.
  • Examples of such monomers are ⁇ , ⁇ -monoethylenically unsaturated mono- and dicarboxylic acids and their amides such as, for example, acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, acrylamide and methacrylamide, also vinyl sulfonic acid and its water-soluble salts and N- Vinyl pyrrolidone.
  • Monomers which usually increase the internal strength of the films in the aqueous polymer dispersion, are also generally copolymerized only in minor amounts, usually 0.5 to 10% by weight, based on the total amount of the monomers to be polymerized.
  • Such monomers normally have an epoxy, hydroxy, N-methylol, carbonyl or at least two non-conjugated ethylenically unsaturated double bonds.
  • these are N-alkylolamides of ⁇ , ⁇ -monoethylenically unsaturated carboxylic acids having 3 to 10 C atoms and their esters with alcohols having 1 to 4 C atoms, among which the N-methylolacrylamide and the N-methylolmethacrylamide are very particularly preferred, two monomers containing vinyl residues, two monomers having vinylidene residues and two alkenyl residues Monomers.
  • the di-esters of dihydric alcohol with ⁇ , ⁇ -monoethylenically unsaturated monocarboxylic acids are particularly suitable, among which in turn acrylic and methacrylic acid are preferably used.
  • monomers having two non-conjugated ethylenically unsaturated double bonds are alkylene glycol diacrylates and dimethacrylates such as ethylene glycol diacrylate, 1,3-butylene glycol diacrylate, 1,4-butylene glycol diacrylate as well as propylene glycol diacrylate, dicinylbenzene, alla methacrylate, methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, methacrylate, methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, vinyl methacrylate, allyl methacrylate
  • the following monomer compositions are of particular interest: 90 to 99% by weight of n-butyl acrylate and / or styrene 1 to 10 wt .-% acrylic acid and / or methacrylic acid.
  • the monomers mentioned are polymerized by the process of free-radical aqueous emulsion polymerization in the presence of polysaccharides, oligosaccharides, monosaccharides and / or their derivatives. They can be of vegetable or animal origin, soluble in water or only dispersible therein.
  • the so-called swelling starches are suitable, which are obtainable, for example, by hydrothermal treatment of native starch.
  • Thin-boiling starches are also suitable. These are starches that are slightly degraded with acids or enzymes or oxidized with mild oxidizing agents, which, even in higher concentrations when cooking with water, do not produce viscous paste but rather relatively thin liquids.
  • acid-modified starches are suitable, which are obtained by heating an aqueous starch suspension below the gelatinization temperature in the presence of small amounts of acid.
  • Oxidatively modified starches are also suitable.
  • Chromic acid, permanganate, hydrogen peroxide, nitrogen dioxide, hypochlorite or periodic acid can be used as the oxidizing agent.
  • all native starches such as cereal starches (e.g. corn, wheat, rice or millet), tuber and root starches (e.g. potatoes, tapioca roots or arrowroot) or sago starches are suitable as starting starches.
  • the use of roasted dextrins as described, for example, in EP-A 408 099 and in EP-A 334 515 is particularly advantageous.
  • dextrins can be obtained by heating moist, dry starch, usually in the presence of small amounts of acid.
  • Typical roasted dextrins are, for example, commercially available white and yellow dextrins; it also includes dextrins that are sold under the trademark Noredux® and Tackidex® are sold.
  • dextrin is used here generally for starch breakdown products.
  • radical emulsion polymerization in the presence of saccharified starches is recommended with particular advantage.
  • This is a starch degradation product obtainable by hydrolysis in the aqueous phase, which preferably has a weight-average molecular weight M w of 2500 to 25,000. More detailed information on the production of the starches and starch derivatives mentioned can be found in G. Tegge, Starch and Starch Derivatives, Behr's Verlag, Hamburg 1984.
  • the starches and starch derivatives mentioned can be used according to the invention in, for example, etherification or esterification in a chemically modified form.
  • This chemical modification can be carried out on the starch before it is broken down or afterwards. Esterifications are possible with both inorganic and organic acids, their ahydrides or chlorides. Phosphated and acetylated derivatives are of particular interest.
  • the most common etherification method is treatment with organic halogen compounds, epoxides or sulfates in aqueous alkaline solution.
  • Particularly suitable ethers are alkyl ethers, hydroxyalkyl ethers, carboxyalkyl ethers and allyl ethers. Cyanoalkylated derivatives and reaction products with 2,3-epoxypropyltrimethylammonium chloride are also suitable. Products that are not chemically modified are preferred.
  • mono- and oligosaccharides as well as cellulose degradation products, for example cellobiose and its oligomers, are also suitable.
  • the saccharified starches of a weight average molecular weight of 2500 to 25,000 to be used with particular preference according to the invention are commercially available as such (for example the C * PUR products 01906, 01908, 01910, 01912, 01915, 01921, 01924, 01932 or 01934 from Cerestar GmbH , D-1150 Krefeld 12).
  • Such saccharified starches are chemically different from roasted dextrins in that hydrolytic degradation in an aqueous medium (usually suspensions or solutions), which is generally carried out at solids contents of 10 to 30% by weight and preferably acid or enzyme-catalyzed, is carried out
  • Possibility of recombination and branching essentially is not given, which is not least expressed in other molecular weight distributions.
  • saccharified starches which have a bimodal molecular weight distribution have proven to be particularly advantageous according to the invention.
  • the production of saccharified starches is generally known and, inter alia, in G. Tegge, Starch and Starch Derivatives, Behr's Verlag, Hamburg 1984, pp. 173 u. Pp. 220 ff and described in EP-A 441 197.
  • the saccharified starches to be used according to the invention are preferably those whose weight-average molecular weight M w is in the range from 4000 to 16,000, particularly preferably in the range from 6500 to 13,000.
  • the saccharified starches to be used according to the invention are normally completely soluble in water at room temperature, the solubility limit generally being above 50% by weight, which proves to be particularly advantageous for the preparation of the aqueous polymer dispersions according to the invention.
  • the saccharified starches to be used according to the invention have an unevenness U (defined as the ratio of weight-average molecular weight M w to number-average molecular weight M n ; U characterizes the molecular weight distribution) in the range from 6 to 12.
  • U is particularly advantageously 7 to 11 and a U of 8 to 10 is very particularly favorable.
  • the proportion by weight of the saccharified starches to be used according to the invention which has a molecular weight below 1000, is at least 10% by weight, but not more than 70% by weight.
  • This weight fraction is particularly preferably in the range from 20 to 40% by weight.
  • the dextrose equivalent DE of which is 5 to 40, preferably 10 to 30 and particularly preferably 10 to 20.
  • the DE value characterizes the reducing power in relation to the reducing power of anhydrous dextrose and is determined according to DIN 10308 edition 5.71, of the standards committee for food and agricultural products (see also Günther Tegge, Starch and starch derivatives, Behr's Verlag, Hamburg 1984, p. 305).
  • aqueous polymer dispersions are obtained in their property profile when using saccharified starches to be used according to the invention
  • the 40 wt .-% aqueous solutions at 25 ° C and a shear rate of 75 s ⁇ 1 one after DIN 53 019 determined dynamic viscosity ⁇ 40 [Pa ⁇ s] from 0.01 to 0.06, preferably from 0.015 to 0.04 and particularly preferably from 0.02 to 0.035.
  • the mono-, oligo-, polysaccharides and / or their derivatives which are present according to the invention during the free radical aqueous emulsion polymerization can nevertheless be present as the only dispersants and also in a mixture with other surface-active substances. If they are used as the sole dispersant, they are normally present in the aqueous polymer dispersions according to the invention in amounts of 1 to 120% by weight, based on the amount of monomers to be polymerized.
  • the protective colloids and emulsifiers normally used as dispersants come into consideration as accompanying surface-active substances.
  • a detailed description of suitable protective colloids can be found in Houben-Weyl, Methods of Organic Chemistry, Volume XIV / 1, Macromolecular Substances, Georg-Thieme-Verlag, Stuttgart, 1961, pp. 411 to 420. Both anionic, cationic and nonionic emulsifiers are also considered.
  • only accompanying emulsifiers are used as accompanying surface-active substances, the relative molecular weights of which, in contrast to the protective colloids, are usually below 2000.
  • emulsifiers are, for example, ethoxylated fatty alcohols (EO degree: 3 to 50, alkyl radical: C8 to C36), ethoxylated mono-, di- and tri-alkylphenols (EO degree: 3 to 50, alkyl radical: C4 to C9), alkali metal salts of dialkyl esters of sulfosuccinic acid and alkali and ammonium salts of alkyl sulfates (alkyl radical: C8 to C12), of ethoxylated alkanols (EO degree: 4 to 30, alkyl radical: C12 to C18), of ethoxylated alkylphenols (EO degree: 3 to 50, Alkyl radical: C4 to C9), of alkyl sulfonic acids (alkyl radical: C12 to C18) and of alkylarylsulfonic acids (alkyl radical: C9 to C18).
  • EO degree: 3 to 50 alkyl radical: C8
  • emulsifiers can be found in Houben-Weyl, Methods of Organic Chemistry, Volume XIV / 1, Macromolecular Substances, Georg Thieme Verlag, Stuttgart, 1961, pages 192 to 208.
  • Accompanying surface-active substances are usually in amounts of up to 5% by weight, based on the amount of the monomers to be polymerized, also used.
  • the emulsion polymerization temperature is usually 30 to 95, preferably 75 to 90 ° C.
  • the polymerization medium can consist only of water, as well as mixtures of water and thus miscible liquids such as methanol. Preferably only water is used.
  • the emulsion polymerization can be carried out either as a batch process or in the form of a feed process, including a step or gradient procedure.
  • the feed process in which part of the polymerization batch is initially charged, heated to the polymerization temperature, polymerized and then the rest of the polymerization batch, usually via a plurality of spatially separate feeds, one or more of which contain the monomers in pure or in emulsified form , gradually or with superposition of a concentration gradient while maintaining the polymerization of the polymerization zone.
  • the initial charge and / or the monomer feed contains small amounts of emulsifiers, based on the total amount of the monomers to be polymerized, as a rule less than 0.5% by weight, in order to reduce the surface tension of the dispersing medium and thus to stir it in facilitate.
  • the monomers are therefore frequently fed to the polymerization zone in a manner pre-emulsified with these auxiliary emulsifiers.
  • the total amount of the mono-, oligo-, polysaccharide and / or their derivatives to be used is advantageously contained in an aqueous receiver.
  • Free radical polymerization initiators are all those which are capable of initiating a free radical aqueous emulsion polymerization. Both peroxides, e.g. Alkali metal peroxidisulfates or H2O2, as well as azo compounds.
  • Combined systems which are composed of at least one organic reducing agent and at least one peroxide and / or hydroperoxide, for example tert-butyl hydroperoxide and the sodium metal salt of hydroxymethanesulfinic acid or hydrogen peroxide and ascorbic acid, are also suitable.
  • Combined systems are also suitable also contain a small amount of a metal compound soluble in the polymerization medium, the metallic component of which can occur in several valence stages, for example ascorbic acid / iron (II) sulfate / hydrogen peroxide, with the sodium metal salt of hydroxymethanesulfinic acid, sodium sulfite, sodium hydrogen sulfite or sodium metal bisulfite and often instead of ascorbic acid of hydrogen peroxide, tert-butyl hydroperoxide or alkali metal peroxydisulfates and / or ammonium peroxydisulfates can be used.
  • a metal compound soluble in the polymerization medium the metallic component of which can occur in several valence stages
  • a metal compound soluble in the polymerization medium for example ascorbic acid / iron (II) sulfate / hydrogen peroxide
  • sodium metal salt of hydroxymethanesulfinic acid sodium sulfite, sodium hydrogen sulfite or
  • the amount of free-radical initiator systems used is 0.1 to 2% by weight, based on the total amount of the monomers to be polymerized.
  • Ammonium and / or alkali metal peroxydisulfates are particularly preferably used by themselves or as a component of combined systems as initiators.
  • Sodium peroxydisulfate is particularly preferably used.
  • the manner in which the free radical initiator system is added to the polymerization vessel in the course of the free radical aqueous emulsion polymerization according to the invention is of minor importance. It can either be completely introduced into the polymerization vessel or used continuously or in stages in the course of the free-radical aqueous emulsion polymerization, depending on its consumption. Specifically, this depends on the chemical nature of the initiator system and on the polymerization temperature in a manner known per se to the person skilled in the art. A portion is preferably introduced and the remainder is fed to the polymerization zone in accordance with the consumption.
  • the free radical aqueous emulsion polymerization according to the invention can of course also be carried out under elevated or reduced pressure.
  • the aqueous polymer dispersions according to the invention are generally prepared with a total solids content of 15 to 65% by weight, those from 10 to 75, very particularly preferably 20 to 60% by weight, based on those to be polymerized, being particularly preferred in terms of application technology Monomers containing mono-, oligo-, polysaccharides and / or their derivatives to be used according to the invention.
  • Suitable binders for abrasive particles for the production of abrasives are, in a very particularly advantageous manner, aqueous polymer dispersions according to the invention, the polymers of which can be obtained by radical polymerisation of monomer mixtures, the following monomer composition consisting of 39 to 69% by weight of at least one ester of 3 to 6 carbon atoms containing ⁇ , ⁇ -monoethylenically unsaturated mono- and dicarboxylic acids and 1 to 6 carbon atoms with alkanols (monomers a), 30 to 60% by weight of styrene (monomer b), 1 to 10 wt .-% of at least one monomer from the group comprising 3 to 6 carbon atoms containing ⁇ , ⁇ -monoethylenically unsaturated carboxylic acids, their amides and nitriles (monomers c) and 0 to 10% by weight of one or more monomers from the group comprising N-alkylol
  • the transfer of the abrasive particles into abrasives can e.g. in such a way that the finely divided abrasive particles are mixed with the aqueous polymer dispersions to be used according to the invention while adjusting the desired binder content, usually (calculated dry) 0.1 to 10% by weight, based on the amount of finely divided starting material, the mixture optionally forms after the addition of known aids, optionally compressed by applying pressure, and then hardens.
  • a so-called base binder layer is preferably first applied to a carrier, into which the abrasive particles are introduced when wet.
  • a second, so-called cover binder layer is generally applied for better embedding and fastening of the grain.
  • the base and cover binder layers can consist of different binders.
  • at least one of the two, preferably the top layer and particularly preferably both, consists of the aqueous polymer dispersions according to the invention.
  • the curing process does not necessarily require the use of elevated temperatures (normally 50 to 250 ° C.), but also left to harden at a satisfactory rate by leaving it at room temperature.
  • elevated temperatures normally 50 to 250 ° C.
  • through-hardening can also be achieved by exposing the mass to be hardened to the action of microwaves.
  • aqueous polymer dispersions according to the invention which are obtainable by free radical aqueous emulsion polymerization of mixtures of monomers a, b, c and d, the monomer composition of which is selected such that a polymer composed only of monomers a, b and c have a glass transition temperature, are recommended with particular advantage in this regard would have in the range of 0 to 40 ° C.
  • aqueous polymer dispersions according to the invention meet these requirements in a completely satisfactory manner.
  • Hardening does not necessarily require elevated temperatures when used, but can be carried out at room temperature and particularly advantageously under the influence of microwaves. This is particularly gentle on the carrier material and avoids extreme water removal, making complicated regeneration of the carrier material in climate zones unnecessary.
  • the binders according to the invention are particularly characterized by increased heat resistance, so that the abrasive grains remain fixed in their position even under the elevated temperatures (150 ° C. and more) that occur during the grinding process. This prevents suppression of the abrasive grains (which reduces the grinding effect) or even chipping.
  • the base layer is applied in dry layer thicknesses of 10 to 100 ⁇ m and the top layer in dry layer thicknesses of 20 to 103 ⁇ m.
  • condensation products based on formaldehyde, melamine, phenol and / or urea for example Urecoll® 118.
  • the amounts to be used can be up to 250% by weight, based on the solids content, determined less the saccharified starch, of the aqueous polymer dispersions according to the invention.
  • the last-mentioned additives only have an advantageous effect in the manner described if curing takes place at elevated temperature, generally 100 to 250 ° C., or in the presence of acid.
  • the latter can be achieved in a simple manner by adjusting the pH of the dispersion medium of the aqueous polymer dispersions to be used according to the invention to 1 to 5, preferably 2 to 3. If heat resistance in the usual range is required, it is preferable to work without additives.
  • the sugared starches mentioned can be characterized as follows: Type M w U % By weight ⁇ 1000 DE ⁇ 40 [Pa ⁇ s] 01906 20080 10.9 12.2 2-5 - 01908 19290 10.0 15.9 8-10 0.056 01910 10540-12640 8.5-9.9 24.7-26.4 11-14 0.030 01915 6680-8350 6.8-8.4 32.9-34.7 17-19 0.021 01921 6700 7.4 39.1 20-23 0.017 01924 4730 6.8 53.6 26-30 0.014 01932 4500 7.9 63.2 33-35 0.011 01934 3000 6.0 68.4 36-39 0.009

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Graft Or Block Polymers (AREA)
  • Polymerisation Methods In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Colloid Chemistry (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
EP92116325A 1991-10-07 1992-09-24 Schleifmittel Expired - Lifetime EP0536596B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4133191A DE4133191A1 (de) 1991-10-07 1991-10-07 Schleifmittel
DE4133191 1991-10-07

Publications (2)

Publication Number Publication Date
EP0536596A1 EP0536596A1 (de) 1993-04-14
EP0536596B1 true EP0536596B1 (de) 1995-09-06

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ID=6442195

Family Applications (1)

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EP92116325A Expired - Lifetime EP0536596B1 (de) 1991-10-07 1992-09-24 Schleifmittel

Country Status (7)

Country Link
US (1) US5221296A (ja)
EP (1) EP0536596B1 (ja)
JP (1) JPH05209167A (ja)
CA (1) CA2079861A1 (ja)
DE (2) DE4133191A1 (ja)
DK (1) DK0536596T3 (ja)
ES (1) ES2075991T3 (ja)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4133193A1 (de) * 1991-10-07 1993-04-08 Basf Ag Waessrige polymerisatdispersionen
US5378252A (en) * 1993-09-03 1995-01-03 Minnesota Mining And Manufacturing Company Abrasive articles
CA2134156A1 (en) * 1993-11-22 1995-05-23 Thomas P. Klun Coatable compositions, abrasive articles made therefrom, and methods of making and using same
DE9419573U1 (de) * 1994-12-07 1995-02-02 Jöst, Peter, 69483 Wald-Michelbach Schleifmittel auf Unterlage
US5618876A (en) * 1995-06-05 1997-04-08 National Starch And Chemical Investment Holding Corporation Latex binders and coatings containing polymers derived from polymerizable saccharide monomers
US5780619A (en) * 1996-06-26 1998-07-14 U.S. Technology Corporation Starch graft poly(meth)acrylate blast media
US6197951B1 (en) * 1996-06-26 2001-03-06 Archer Daniels Midland Company Starch graft copolymer blast media
US6251353B1 (en) * 1996-08-26 2001-06-26 Bridgestone Corporation Production method of silicon carbide particles
AUPO216396A0 (en) 1996-09-06 1996-10-03 Ici Australia Operations Proprietary Limited Stain resistant water-borne paint
US6162268A (en) * 1999-05-03 2000-12-19 Praxair S. T. Technology, Inc. Polishing slurry
US6569214B2 (en) * 2000-06-01 2003-05-27 U.S. Technology Corporation Composite polymer blast media
CN1318485C (zh) * 2004-02-24 2007-05-30 中国科学院化学研究所 改变聚合物材料表面浸润性的方法
DE102007030102B4 (de) * 2007-06-28 2019-10-31 Schoeller Technocell Gmbh & Co. Kg Vorimprägnat
EP2540445B1 (de) * 2011-06-29 2013-09-18 Hermes Schleifkörper GmbH Verfahren zur Herstellung eines Werkzeugs aus gebundenem Schleifmittel
FR2983758B1 (fr) * 2011-12-13 2015-11-27 Saint Gobain Abrasives Inc Composition resinique aqueuse pour articles abrasifs et articles resultants.
FR2983759B1 (fr) * 2011-12-13 2014-08-01 Saint Gobain Abrasives Inc Composition resinique aqueuse pour articles abrasifs et articles resultants.
EP3166978B1 (de) * 2014-07-10 2018-05-16 Basf Se Verfahren zur herstellung gefrier-auftau-stabiler, waessriger dispersionen

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4690692A (en) * 1977-08-25 1987-09-01 Hoechst Aktiengesellschaft Synthetic resin binders and their use for the manufacture of abrasives
DE3046696C2 (de) * 1980-12-11 1984-11-22 Rex Patent Graf von Rex GmbH & Co KG, 7170 Schwäbisch Hall Verfahren zur Herstellung von Reibbelägen sowie Reibbeläge
US4350498A (en) * 1980-12-24 1982-09-21 Norton Company Dampening agent for resin bonded grinding wheels
DE3323804A1 (de) * 1983-07-01 1985-01-03 Wacker-Chemie GmbH, 8000 München Verfahren zur herstellung waessriger polymerdispersionen und ihre verwendung
US4652274A (en) * 1985-08-07 1987-03-24 Minnesota Mining And Manufacturing Company Coated abrasive product having radiation curable binder
US4773920B1 (en) * 1985-12-16 1995-05-02 Minnesota Mining & Mfg Coated abrasive suitable for use as a lapping material.
AT389883B (de) * 1986-08-21 1990-02-12 Igel Schleifmittel Schleifmittelzusammensetzung bzw. schleifmittel und verfahren zu deren herstellung
US5055113A (en) * 1988-11-23 1991-10-08 Minnesota Mining And Manufacturing Company Abrasive product having binder comprising an aminoplast resin

Also Published As

Publication number Publication date
EP0536596A1 (de) 1993-04-14
US5221296A (en) 1993-06-22
DE4133191A1 (de) 1993-04-08
DK0536596T3 (da) 1995-10-23
JPH05209167A (ja) 1993-08-20
CA2079861A1 (en) 1993-04-08
DE59203558D1 (de) 1995-10-12
ES2075991T3 (es) 1995-10-16

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