Abstract: The present invention relates to a method of producing a sulfur-containing transparent polymer by polymerizing a composition containing a (metha)acrylate monomer having sulfur in its molecule, characterized by radical polymerization of a composition containing at least one compound selected from radical chain transfer compounds and radical trapping compounds in an amount of 0.1 to 7.0% by weight of the total amount of the composition. The polymer obtained by polymerization is less colored. The method can provide a polymer having a high total light transmittance, a high refractive index and a light weight and is hardly yellowed during use.

Abstract: The invention relates to a multi-component dental cement which contains as a first component an ethylenically unsaturated polymerisable compound, as a second component calcium hydroxide, calcium oxide or a precursor thereof and also a polymerisation initiator, the constituents of which can be contained in one or more cement components, which is characterized in that the ethylenically unsaturated polymerisable compound has both at least one .beta.-dicarbonyl group and also at least one acrylic, alkacrylic or vinyl aromatic group. Also included are a process for the production of a multi-component dental cement and the use of the described polymerisable .beta.-dicarbonyl compounds in calcium hydroxide dental cements.

Abstract: A functional group-containing porous resin prepared by polymerization of a monomer mixture of, based on 100% by weight of the total amount of the monomers, 15 to 97% by weight of divinylbenzene, 0 to 82% by weight of at least one aromatic monovinyl monomer selected from the group consisting of styrene, methylstyrene and ethylvinylbenzene and 3 to 30% by weight of a vinylbenzyloxyalkyl derivative represented by the formula ##STR1## wherein n is an integer of 2 to 16 and A represents a hydroxyl group or a halogen atom, and a process for preparing the same. The above-mentioned porous resin of the invention can fully exhibit its function due to the marked presence of a functional group on the surface of the resin and/or in the neighborhood thereof.

Abstract: A process is provided for preparing a high-quality methyl methacrylate polymer by polymerizing a monomer comprising methyl methacrylate as a main component in the presence of a radical polymerization initiator, a chain transfer agent, and 5 to less than 10 wt. % methanol. The polymerization is carried out in a uniform solution. According to this process, a methyl methacrylate polymer is obtained which reduces the generation of silver streaks, voids, coloring, odor and the like at the time of thermal molding.

Abstract: High temperature polymerization process and products obtained therefrom are provided. The polymerization is conducted at above 225.degree. C. to produce polymers having a degree of polymerization below 50. The products are useful as detergent additives and for subsequent polymerization.

Abstract: An immobilized Lewis Acid catalyst system for the carbocationic polymerization of olefin monomer is provided. The catalyst comprises a porous polymer support having catalytically active Lewis Acid residue bonded to the surface of the support including the pore surfaces.

Abstract: Living random (meth)acrylic copolymers, facilely converted into random co(meth)acrylates and block copolymers thereof, comprise the anionic copolymerizates of at least one comonomer A with at least one comonomer B selected from among the (meth)acrylates and maleimides, at least one of the comonomers A and B comprising a (meth)acrylate, in the presence of (i) at least one alkali or alkaline earth metal, mono- or difunctional initiator and (ii) at least one ligand, for example a nonnitrogenous macrocyclic complexant, e.g., a crown ether, or an alkali metal alcoholate.

Abstract: Polyisoolefins are obtained using the process according to the invention by polymerising isoolefins, optionally with conjugated or unconjugated dienes and/or cationically polymerisable, mono- or polyunsaturated compounds at temperatures of -100.degree. C. to +100.degree. C. and pressures of 0.1 to 100 bar in solution, in suspension or in the gas phase in the presence of initiator systems consisting of certain hydrocarbons and open-chain and/or cyclic aluminoxane compounds.

Abstract: A method for the production of a microsphere without use of a dispersion stabilizer is disclosed which permits the microsphere to be produced in the form of discrete particles readily treatable for purification. The method which produces this microsphere comprises the steps of dissolving in an organic solvent such as an alcohol a monomer mixture including an ethylenically unsaturated amide and 10 to 70% by weight, based on 100% by weight of said monomer mixture, of a cross-linking agent thereby preparing a mixed solution, keeping said mixed solution at a temperature in the range of from 30.degree. to 95.degree. C., and adding thereto at least one initiator selected from the group consisting of peroxide type initiators and azo type initiators in an amount such as to be contained therein at a final concentration in the range of from 1.times.10.sup.-5 to 8.times.10.sup.-2 mol/liter thereby inducing polymerization of said monomer mixture.

Abstract: A polymerization process comprising: heating a mixture comprised of a free radical initiator, a stable free radical agent, at least one polymerizable monomer compound, and optionally a solvent, to form a polymer with a high monomer to polymer conversion and a narrow polydispersity, wherein said polymer is comprised of a covalently bound free radical initiator fragment at one end and a covalently bound stable free radical compound at the other end of the polymer, and wherein said stable free radical agent has high thermal, acidic, and photochemical stability.

Abstract: The present invention provides a method for producing a perfluorocarbon copolymer containing functional groups, which comprises:emulsifying a perfluorocarbon monomer containing a functional group represented by the following general formula (1) into fine dispersions having an average diameter of 2 .mu.m or less in water:CF.sub.2 .dbd.CF--O--(CF.sub.2 CF(CF.sub.3)--O)n--(CF.sub.2)m--Z(1)wherein m is an integer of 2 to 4; Z is CO.sub.2 R (where R represents an alkyl group having 1 to 3 carbon atoms) or SO.sub.2 F; n is 1 or 2 when Z is CO.sub.2 R and n is an integer of 0 to 2 when Z is SO.sub.2 F,adding at least one water-soluble organic chain transfer agent selected from the group consisting of aliphatic alcohols having 1 to 6 carbon atoms and ethers having 2 to 6 carbon atoms andpolymerizing the perfluorocarbon monomer (1) containing a functional group with tetrafluoroethylene represented by the following formula (2):CF.sub.2 .dbd.CF.sub.2 (2).

Abstract: A process is provided for preparing a high-quality methyl methacrylate polymer by polymerizing a monomer comprising methyl methacrylate as a main component in the presence of a radical polymerization initiator, a chain transfer agent, and a small amount of methanol as a solvent. The polymerization is carried out in a uniform solution at a temperature of 90.degree. to 180.degree. C. so that a monomer conversion of 40 to 90 mol % is attained. According to this process, a methyl methacrylate polymer is obtained which reduces the generation of silver streaks, voids, coloring, odor and the like at the time of thermal molding.

Abstract: Epoxy-containing compounds which are essentially free of organic halides are prepared by (I) reacting an allyl derivative of an active hydrogen-containing compound with (II) a peroxygen-containing compound. The epoxy-containing compounds are useful in coatings, castings, laminates etc.

Abstract: A process for preparing a poly(hydroxystyrene) which comprises the steps of (a) heating a carbinol under decomposition conditions in the presence of a solvent for a sufficient period of time to form hydroxystyrene, said solvent having a boiling point in substantially the same range as said hydroxystyrene; and (b) polymerizing said hydroxystyrene under suitable polymerization conditions of pressure and temperature and for a sufficient period of time to form poly(hydroxystyrene).

Abstract: In a process for the homogeneous polymerization of water insoluble polymers containing greater than 50% by weight of monomers selected from the group consisting of C.sub.1 -C.sub.18 acrylate or methacrylate esters, N-substituted acryl or methacrylamides and mixtures thereof in substantially non-aqueous organic solutions, the improvement which comprises using as the polymerization initiator a water soluble initiator dissolved in sufficient amount of water to dissolve the initiator whereby the resultant polymer is characterized by lower residual monomer levels than are obtained using equivalent amounts of water-insoluble initiators.

Abstract: Gel-free ethylene/vinyl acetate copolymers with a high content of copolymerized vinyl acetate and a high Mooney viscosity are produced by carrying out the polymerization in solution in the presence of 20 to 45% by weight tert.butanol, based on the reaction solution, at temperatures of 50.degree. to 80.degree. C. and under pressures of 300 to 450 bar using azo compounds in a cascade of stirred reactors with an average residence time of the reaction solution in the reactor cascade of 5 to 9 hours and a conversion of 50 to 70% by weight, based on the vinyl acetate used. The ethylene/vinyl acetate copolymers produced by the process according to the invention may be used for the production of vulcanizates having improved mechanical properties.

Abstract: A propylene, .alpha.-olefin copolymer, where the .alpha.-olefin has 5 or more carbon atoms made with a metallocene catalyst system provides substantially higher cold flow resistance from when the propylene copolymer is made with an .alpha.-olefin having 4 or less carbon atoms. Other properties such as ultimate tensile strength and impact strength are substantially higher as well. Such polymers can be used to advantage in fibers, fabrics, and oriented films.

Abstract: Polymers that can be obtained by suspension polymerization of 50 to 100% by weight of at least one compound selected from the group comprising C.sub.1 -C.sub.18 -alkyl esters of acrylic acid and methacrylic acid, and 0 to 50% by weight of further, free radical-polymerizable monomers in the presence of a buffer selected from the group comprising citric acid, alkali metal citrates, alkaline earth metal citrates and ammonium citrates, and also a process for preparing these polymers and their use in the production of molded articles.

Abstract: Living random (meth)acrylic copolymers, facilely converted into random co(meth)acrylates and block copolymers thereof, comprise the anionic copolymerizates of at least one comonomer A with at least one comonomer B selected from among the (meth)acrylates and maleimides, at least one of the comonomers A and B comprising a (meth)acrylate, in the presence of (i) at least one alkali or alkaline earth metal, mono- or difunctional initiator and (ii) at least one ligand, for example a nonnitrogenous macrocyclic complexant, e.g., a crown ether, or an alkali metal alcoholate.

Abstract: Chlorine-free, non-drying copolymer of isobutene with C.sub.4 -C.sub.10 -dienes having isolated or conjugated double bonds and containing at least 60 mol % of terminal double bonds, and a process for their preparation.

Abstract: Suspension-polymerized, crosslinked copolymers of methacrylic anhydride yield beads suitable as precursors for weak-acid and other ion exchange resins, affinity chromatography materials and other materials which require spherical polymers having reactive anhydride groups for their preparation. Both gel and macroporous beads of these copolymers may be made by the process of the invention.

Abstract: A polymerization process comprising: heating a mixture comprised of a free radical initiator, a stable free radical agent, at least one polymerizable monomer compound, and optionally a solvent, to form a polymer with a high monomer to polymer conversion and a narrow polydispersity, wherein said polymer is comprised of a covalently bound free radical initiator fragment at one end and a covalently bound stable free radical compound at the other end of the polymer, and wherein said stable free radical agent has high thermal, acidic, and photochemical stability.

Abstract: Radical (co)polymerization process of fluorinated olefinic monomers, optionally in association with one or more non-fluorinated olefins, in which the monomers are (co)polymerized in aqueous emulsion, in the presence of a hydrogenated chain transfer agent selected from hydrogen, aliphatic hydrocarbons and fluorohydrocarbons C.sub.1 -C.sub.20 and of a branched chain aliphatic alcohol C.sub.3 -C.sub.12 characterized by a ratio between the number of hydroxyl groups and the number of methyl groups lower than or equal to 0.5.

Abstract: A process is disclosed for the continuous production, with reduced gel formation, of free radical addition polymers from ethylenically unsaturated monomers containing at least one free hydroxyl group such as 2-hydroxyethyl methacrylate, from about 0 to about 5% by weight of an alpha-beta unsaturated carboxylic acid such as acrylic acid or methacrylic acid, and the remainder of the monomers used are free radical addition copolymerizable compounds such as styrene, methyl methacrylate and butyl acrylate. The free radical addition polymerization is conducted at from about 150.degree. C. to about 310.degree. C. under superatmospheric pressure in the presence of one or more solvents. The solvent or the volume average of the solvent mixture has an overall calculated root mean square value of the hydrogen bonding and polar contributions of each solvent's solubility parameters in the range of from about 6 to about 15.

Abstract: An improved process for the continuous copolymerization of ethylene with certain polar comohomers having reactive double bonds is disclosed wherein reactor fouling is significantly reduced or eliminated by use of surfactants.

Abstract: A process for forming dielectric particles includes admixing a vinyl halide monomer and a crosslinker in a liquid dispersion medium to form a first mixture. A second mixture of an initiator and a stabilizer is prepared and added to the first mixture to form a third mixture in which the monomer polymerizes to form white crystalline polymer particles which are sonified for uniformity. The particles may be stained by exposure to a dehydrohalegenation reagent and dispersed in an electrophoretic fluid for use in an electrophoretic display.

Abstract: Polysuccinimide is prepared by reacting an unsaturated C.sub.2 dicarboxylic acid or anhydride thereof, e.g., maleic acid, fumaric acid, and maleic anhydride, with a particulate ammonium salt that is thermally decomposable to liberate ammonia. The reaction is carried out at a temperature which is above the thermal decomposition temperature of the ammonium salt and for a time period which is sufficient for the acid or anhydride to react with the ammonia liberated from the ammonium salt and for polymerization to occur. The present method avoids the prior art problems of controlling ammonia losses and water removal. The product polysuccinimide can be readily hydrolyzed to polyaspartic acid or a salt thereof, if desired.

Abstract: Novel hydroxy peroxides of the Structure AHO--R.sub.11 --X--OO--R (A)[wherein R--, --R.sub.11 -- and --X-- are as defined in the Summary of the Invention Section], having 10 hour half-life temperatures of 85.degree.-100.degree. C., the processes for their preparation, and the use of these novel compositions in curing of unsaturated polyester resins and in initiating polymerization of ethylenically unsaturated monomers.

Abstract: Spherical monodispersed polymeric particles are prepared from vinyl monomers and crosslinking polymerizable polyvinyl monomers. More particularly, a novel process for producing spherical monodispersed gel particles that are about 1-6 .mu.m in size and contain at least about 0.5 to about 3 weight percent (based on polymerizable vinyl monomer/vinyl polymer) of a polymerizable polyvinyl monomer is disclosed. The process comprises the steps of combining an isoalkanol solvent, a polymerizable vinyl monomer and a crosslinking polymerizable polyvinyl monomer under timed and monitored conditions.

Abstract: A process for preparing highly reactive polyisobutenes with a content of terminal vinylidene groups of more than 80 mol % and an average molecular weight of 500-5000 Dalton by the cationic polymerization of isobutene or isobutene-containing hydrocarbon feeds in liquid phase with the aid of boron trifluoride as catalyst and at from 0.degree. C. to -60.degree. C., comprises polymerizing in the presence of secondary alcohols with 3-20 carbon atoms and/or ethers with 2-20 carbon atoms.

Abstract: Described are preferred processes for producing linear polyvinylpyridines. The processes involve the use of hydrogen peroxide to initiate polymerization of vinylpyridine monomers in an alcohol/water solvent. Processes of the invention provide good reaction rates and conversions, and are particularly advantageous in achieving control of the M.sub.w 's of the final product polymers.

Abstract: Process for producing polyvinyl ester having a high degree of polymerization and an intrinsic viscosity of from 15 dl g.sup.-1 to 3.2 dl g.sup.-1, and a polyvinyl ester obtained thereby. The process comprises subjecting a vinyl ester monomer to emulsion polymerization using nonionic emulsifiers nonionic-anionic emulsifiers, or anionic emulsifiers and a redox initiator at a temperature of -60.degree. to 15.degree. C.

Abstract: The present invention discloses an alkylidenenorbornene polymer comprising as the essential constituent at least one kind of the structural unit represented by the formula ##STR1## wherein R.sub.1 denotes an alkyl group of 1-4 carbon atoms and R.sub.2 denotes a hydrogen atom or an alkyl group of 1-5 carbon atoms, and a process for producing the same.According to the present invention, an alkylidenenorbornene polymer is obtained which is excellent in light resistance, transparency, heat resistance and moisture resistance and is useful as an optical polymeric material.

Abstract: A process for the polymerization of polymers of itaconic acid and vinyl acetate comprising the step of polymerizing(i) from 10 to 95 mole percent of monomer units of the formula I: ##STR1## wherein each of R.sub.1 and R.sub.2, which may be the same or different, represents a hydrogen atom, a methyl group or an ethyl group, and M is a hydrogen atom or an alkyl (C.sub.1 to C.sub.18) chain or an organic group such as an amino containing functionality;(ii) from 5 to 90 mole percent of monomer units of the formula II: ##STR2## wherein R.sub.3 represents a hydrogen atom or the group --COCH.sub.3 ; and(iii) from 0 to 45 mole percent of a ethylenically unsaturated copolymerizable comonomer, said polymerization being carried out using semi-batch polymerization procedures at a temperature of 60.degree. to 200.degree. C. in the presence of a substantially anhydrous alcoholic solvent.

Abstract: A method for producing polysuccinimide is provided. Thermal polymerization of maleamic acid at a temperature of from about 160.degree. C. to about 330.degree. C. produces polysuccinimide. The reaction is optionally conducted in the presence of one or more processing aids, solvents or diluents. The polysuccinimide is particularly useful as a detergent additive.

Abstract: A homogeneous, random interpolymer of ethylene and an alpha-olefinically unsaturated carboxylic acid or ester having a melt flow rate in the range of about 0.1 to about 300 g/10 minutes, as determined by ASTM D-1238 (190.degree. C./2160 g), is improved during its manufacture when made in a substantially constant environment in a stirred autoclave under substantially steady-state conditions of temperature, pressure, and flow rates, said temperature and pressure being sufficient to produce a single phase reaction, using a free-radical initiator, said improvement being obtained by the use of a minor amount of a telogenic modifier in the reaction mixture, the process being further characterized by the use of either, or both, of (a) a temperature which is lower than that which would be required without the presence of the telogen, or (b) a pressure which is higher than that which would be required without the presence of the modifier.

Abstract: Paste-forming polymers of vinyl chloride are produced by discontinuous polymerization in the presence of a conventional predispersion of emulsifier, dispersion acid, water and optional monomer-soluble catalyst. The predispersion is prepared only with 30-80% by weight of the amount of emulsifier required in total. The remainder of the emulsifier, or a component forming the emulsifier, is added in metered amounts as an aqueous solution batchwise or continously to the polymerization mixture after a conversion of 10-60% by weight.The thus-obtained polymers lead to pastes of an especially low viscosity, even under high shear stress, and result in open-cell plasticized foam materials having a good elastic memory capacity.

Abstract: An improved solution polymerization process is provided wherein vinyl monomers are polymerized in the presence of at least one reactive modifier which is a substituted alpha-olefin that incorporates at least three ether groups, is hydrophilic, and has a molecular weight of at least about 200. The modified vinyl polymers so produced are characterized by various improved physical properties including, in particular, electrical characteristics such as antistatic capacity.

Abstract: Aqueous emulsions of a polymerization initiator are used for suspension (co)polymerization reactions. The aqueous emulsions contain: (a) an organic peroxide which is liquid at -5.degree. C.; (b) an aliphatic monohydric alcohol having 1-4 carbon atoms and/or aliphatic glycol having 2-4 carbon atoms; (c) a surfactant and/or a protective colloid; and (d) water. The emulsions may be transported while in a liquid state at a temperature of -10.degree. C. to -25.degree. C. with minimal decrease in active oxygen content.

Abstract: A process for making a solution of PVP K-90 polymer having a weight average molecular weight, Mw, of about 630,000 to 750,000 and a molecular weight distribution, Mw/Mn, where Mn is the number average molecular weight of the polymer, of 5 or less, which comprises free radical polymerizing about 5-30% by weight vinylpyrrolidone, preferably 10-20%, at about 40.degree.-100.degree. C., preferably 60.degree.-75.degree. C., in an aqueous-alcohol solvent selected from the group consisting of about (a) 5% isopropanol-95% water, (b) 10% ethanol-90% water and (c) 20% methanol-80% water.

Abstract: A water-dispersible, inherently tacky pressure-sensitive adhesive comprising a tacky emulsion polymer formed of from about 80% to 90% by weight of monomers comprising a major portion of at least alkyl acrylate containing from 4 to about 8 carbon atoms in the alkyl group and from about 20% to 10% by weight hydroxyethyl methacrylate, said emulsion polymer formed in the presence of anionic and nonionic surfactants to provide a polymer having a glass transition temperature of -15.degree. to -50.degree. C. A sufficient amount of chain transfer agent is employed to provide an emulsion polymer which when coated on a repulpable paper substrate enables recovery of paper fibers substantially free of adhesive under conditions of TAPPI Useful 204, and is resistant to loss of adhesive properties on exposure to high humidity.

Abstract: A finishing process for a polymer containing an active catalyst residue. Starting polymer has a crystallinity of less than 10 percent by weight and is maintained in an essentially oxygen free reaction zone at a temperature less than polymer sticking temperature. The polymer is stabilized and acids neutralized by adding 2, 6-di-tert-butyl-4-alkyl phenol and/or alkyl -3-(3-5 -di-tert-butyl-4-hydroxy phenyl)- propionate and zinc oxide, hydrotalcite, or a zeolite. Resulting polymer is then treated with catalyst deactivators including water, and then mixed with photo-oxidative stabilizers.

Abstract: This invention relates to an improved process for producing a clear solution of vinylpyrrolidone (VP) and vinyl acetate (VA) monomers which comprises, in an anhydrous system,(a) reacting a C.sub.2 to C.sub.3 alcoholic solution containing said VA monomer and between about 60 and about 80 wt. % portion of total VP monomer in the presence of between about 0.05 and about 0.3 wt. % of a free radical initiator selected from the group consisting of tertamylperoxy pivalate and 2,2-azobis(2-methylbutyronitrile) or a mixture thereof for a period of from about 5 to about 10 hours, at a temperature between about 60.degree. and about 110.degree. C.;(b) gradually adding the remaining VP monomer in C.sub.2 to C.sub.3 alcohol solution at reaction temperature after the addition of the VA monomer is complete;(c) raising the temperature of the resulting reaction mixture to between about 110.degree. and about 150.degree. C.;(d) continuing the polymerization reaction at said higher temperature in the presence of from about 0.

Abstract: Improved monodisperse spheroidal particle latices of vinyl chloride polymers, e.g., having particle sizes ranging from 0.17 to 0.8 .mu.m or from 0.5 to 1.2 .mu.m, are produced by aqueous emulsion polymerization of vinyl chloride monomer, whether in a single stage or in two stages, in the absence of surface-active agent, in the presence of at least 0.2% by weight of at least one water-soluble alkali metal or ammonium persulfate initiator, and also in the presence of at least one water-soluble auxiliary compound that is a solvent for vinyl chloride, in such amount that the solubility of vinyl chloride in the aqueous phase at 25.degree. C. at atmospheric pressure is at least 1.5 g/l.

Abstract: A process for preparing highly reactive polyisobutenes with a content of terminal vinylidene groups of more than 80 mol % and an average molecular weight of 500-5000 Dalton by the cationic polymerization of isobutene or isobutene-containing hydrocarbon feeds in liquid phase with the aid of boron trifluoride as catalyst and at from 0.degree. C. to -60.degree. C., comprises polymerizing in the presence of secondary alcohols with 3-20 carbon atoms and/or ethers with 2-20 carbon atoms.

Abstract: A process for making a biodegradable aliphatic polyester and the polyester so formed is disclosed. The process comprises copolymerizing a cyclic ketene acetal having the structural formula ##STR1## where R is a bivalent moiety, and an olefin. This copolymerization occurs in a solution of a tertiary alcohol and in the presence of a free radical initiating effective amount of a compound having the structural formula ##STR2## where R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 are the same or different and are C.sub.1 -C.sub.20 hydrocarbyl, C.sub.1 -C.sub.20 hydrocarbyloxy, cyano, halogen, carboxy, carboalkoxy, carbonyl or formyl. The copolymerization occurs at a temperature in the range of between in excess of ambient temperature and less than 100.degree. C. and at a pressure in excess of about 2,000 psi.

Abstract: Copolymers suitable for use as temporary surface protection for two- or three-dimensional structures and as sizing agents are based on C.sub.1 -C.sub.8 -alkyl acrylates and/or methacrylates and are obtainable by free radical emulsion or solution polymerization ofA) from 50 to 95% by weight of a C.sub.1 -C.sub.8 -alkyl acrylate or methacrylate,B) from 5 to 20% by weight of an unsaturated carboxylic acid or anhydride,C) from 0 to 20% by weight of further water-soluble comonomer, andD) from 0 to 10% by weight of other comonomer in the presence ofE) from 2 to 60 parts by weight of a polyvinyl alcohol per 100 parts by weight of the monomer mixture of A) to D).

Abstract: An accelerator composition for the curing of unsaturated maleic, allylic, vinylic and epoxy-type polyester resins is disclosed. The accelerator composition includes a complex of a salt of a metal selected from lithium, copper, manganese, magnesium, vanadium, iron and cobalt, with an oxygen-containing compound which is capable of forming a complex with the metal salt and includes at least one functional group selected from aldehyde, ketone, ether, ester and alcohol. Also disclosed are a curable resin composition including the foregoing accelerators and a curing process employing these accelerators.

Abstract: Copolymers suitable for use as temporary surface protection for two- or three-dimensional structures and as sizing agents are based on C.sub.1 -C.sub.8 -alkyl acrylates and/or methacrylates and are obtainable by free radical emulsion or solution polymerization ofA) from 50 to 95% by weight of a C.sub.1 -C.sub.8 -alkyl acrylate or methacrylate,B) from 5 to 20% by weight of an unsaturated carboxylic acid or anhydride,C) from 0 to 20% by weight of further water-soluble comonomer, andD) from 0 to 10% by weight of other comonomer in the presence ofE) from 2 to 60 parts by weight of a polyvinyl alcohol per 100 parts by weight of the monomer mixture of A) to D).

Abstract: A hardenable copolymer containing copolymerization molecular constituents from a fluorinated monomer and an allylic compound, characterized in that:(a) the fluorinated monomer molecular constituents originate from the combination of tetrafluoroethylene and chlorotrifluoretyhylene,(b) the molecular constituents from the allylic compound originate from an allylic polyol of formula: ##STR1## in which R.sub.1 is H or CH.sub.2 OH, R.sub.2 is OH or CH.sub.2 OH, R.sub.3 is CH.sub.3 or OH, with the condition that R.sub.1 and R.sub.3 cannot be simultaneously H and CH.sub.3, and that it also contains (c) copolymerization molecular constituents from a vinylic ether of formula:CH.sub.2 .dbd.CH--O--Rin which R is a linear or branched chain alkyl radical with 2 to 13 carbon atoms, and the process of making such copolymers and paints and varnishes containing the same.