A clear homogenous, efficient, MEKO-free anti-skinning composition, for use in alkyd-based coating materials containing metal carboxylate driers, contains a mixture of cyclohexanone oxime and/or a petroleum distillate soluble zinc carboxylate dissolved in methyl propyl ketoxmine.

A clear homogenous, efficient, MEKO-free anti-skinning composition, for use in alkyd-based coating materials containing metal carboxylate driers, contains a mixture of cyclohexanone oxime and/or a petroleum distillate soluble zinc carboxylate dissolved in methyl propyl ketoxmine.

Fluoroelastomer compositions comprising fluoroelastomers having copolymerized units of a nitrile-containing cure site monomer are cured with certain hydrazone or oxime curatives.

Fluoroelastomer compositions comprising fluoroelastomers having copolymerized units of a nitrile-containing cure site monomer are cured with certain hydrazone or oxime curatives.

The invention relates to a coating composition comprising an oxidatively drying binder and an anti-skinning agent, the anti-skinning agent comprising: a) a diketone of formula (I) (b) an aldoxime or ketoxime of formula (II) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and n have the same meaning as that defined by the present application. ##STR00001##

The invention relates to a coating composition comprising an oxidatively drying binder and an anti-skinning agent, the anti-skinning agent comprising: a) a diketone of formula (I) (b) an aldoxime or ketoxime of formula (II) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and n have the same meaning as that defined by the present application. ##STR00001##

The invention pertains to a (per)fluoroelastomer composition comprising: a (per)fluoroelastomer [fluoroelastomer (A)]; and at least one (per)fluoropolyether additive [polymer (E)] comprising a (per)fluoropolyether chain comprising recurring units having at least one catenary ether bond and at least one fluorocarbon moiety, and comprising at least one chain end comprising at least one per(halo)fluorinated aromatic group [group (AO], said polymer (E) being comprised in the composition in an amount of 0.5 to 30 phr, with respect to fluoroelastomer (A).

The invention pertains to a (per)fluoroelastomer composition comprising: a (per)fluoroelastomer [fluoroelastomer (A)]; and at least one (per)fluoropolyether additive [polymer (E)] comprising a (per)fluoropolyether chain comprising recurring units having at least one catenary ether bond and at least one fluorocarbon moiety, and comprising at least one chain end comprising at least one per(halo)fluorinated aromatic group [group (AO], said polymer (E) being comprised in the composition in an amount of 0.5 to 30 phr, with respect to fluoroelastomer (A).

Method for preparation of 5-alkylsalicylaldoximes with formula 1, where R is a C6-C16 alkyl group, consisting in that into a water-alcohol solvent system, p-alkylphenol, sodium hydroxide, chloroform and hydroxylamine are introduced, while in relation to the alkylphenol used, sodium hydroxide and chloroform are used in amounts from the stoichiometric amount to a 100% excess, and hydroxylamine is used in amounts from the stoichiometric amount to a 60% excess, and the reaction is carried out at a temperature of 60-75? C. for 1.5-4 h, and then, at a temperature of 20-30? C., the post-reaction mixture is acidified till the pH of the aqueous phase <7.0 is obtained, and next, an alcohol-water azeotrope is distilled off with an admixture of unreacted chloroform, the residue is mixed with a neutral C5-C10 hydrocarbon solvent, the layers are separated, and the solvent is distilled off from the organic phase.

Method for preparation of 5-alkylsalicylaldoximes with formula 1, where R is a C6-C16 alkyl group, consisting in that into a water-alcohol solvent system, p-alkylphenol, sodium hydroxide, chloroform and hydroxylamine are introduced, while in relation to the alkylphenol used, sodium hydroxide and chloroform are used in amounts from the stoichiometric amount to a 100% excess, and hydroxylamine is used in amounts from the stoichiometric amount to a 60% excess, and the reaction is carried out at a temperature of 60-75? C. for 1.5-4 h, and then, at a temperature of 20-30? C., the post-reaction mixture is acidified till the pH of the aqueous phase <7.0 is obtained, and next, an alcohol-water azeotrope is distilled off with an admixture of unreacted chloroform, the residue is mixed with a neutral C5-C10 hydrocarbon solvent, the layers are separated, and the solvent is distilled off from the organic phase.