Patent classifications
C08F118/02
Acrylic resins and powder coating compositions and powder coated substrates including the same
An epoxy functional acrylic resin having a T.sub.g of greater than 85° C. and a calculated solubility parameter from about 9.20 to about 9.30 (cal/cm.sup.3).sup.1/2, powder coating compositions including the same and coated substrates coated with the powder coating composition is described. The resin includes, as copolymerized monomers, from about 10 wt. % to about 40 wt. % of one or more epoxy functional unsaturated monomers; from about 10 wt. % to about 20 wt. % of one or more hydrophobic acrylic monomers, and from greater than 50 wt. % to about 75 wt. % of at least one nonionic copolymer that is different from the hydrophobic acrylic monomers ii), each monomer wt. % based on the total weight of copolymerized monomers in the resin.
Fluorine-containing polymer microsphere
Disclosed in the invention is a fluorine-containing polymer microsphere. A polymerization monomer, a photoinitiator and a stable dispersant are added into a reaction kettle, carbon dioxide gas is introduced for emptying air therein, then liquid carbon dioxide is injected, an initiating light source is used for irradiating in the reaction kettle after the temperature and pressure of the reaction kettle are constant, the reaction is performed under the conditions of −20-30° C. and 20-70 bar, wherein the concentration of the polymerization monomer accounting for the total volume of the reactants is 0.02-2 g/ml, and the weight ratio of the photoinitiator, stable dispersant and polymerization monomer is (0.3-10):(2-20):100; after the reaction is finished, the temperature returns to room temperature, and the precipitate is washed with liquid carbon dioxide, so as to obtain the polymer microspheres. The fluorine-containing polymer which covers the surface of the microspheres in the present invention can reduce the surface energy thereof, and can benefit the timely migration of the microspheres to the coating surface; a tertiary amine group is introduced into the fluorine-containing polymer to firmly bond the microspheres into a cross-linked network, and thus benefits the tight integration of the microspheres and the coating; a RAFT active group is introduced to firmly anchor the microspheres onto the coating film; thus ensuring the stability of the cured coating.
Water absorbent polymers and a process for their preparation
Water absorbent polymers and a process for their preparation are disclosed. The process for preparing water absorbent polymers comprises preparing a slurry with relatively high amounts of polymer particles (in the range of 40 to 55 wt % of the total mass of the slurry) having water absorbed therein. The slurry is then directly spray dried to obtain water absorbent polymers.
Methods for converting glycerol to allyl compounds
The present disclosure is directed towards methods of converting glycerol to an allyl compound, involving deoxydehydrating glycerol with formic acid and heat to form allyl alcohol; and esterifying the allyl alcohol with formic acid and/or phthalic anhydride and heat to form allyl formate and diallyl phthalate. In some instances, the heat is generated by a microwave. In further instances, the methods involve polymerizing the allyl alcohol, allyl formate and/or diallyl phthalate to form poly(allyl alcohol) or poly(allyl formate) or poly (diallyl phthalate). In some instances, the allyl polymers were used for the consolidation of oil sands tailings.
METHODS FOR CONVERTING GLYCEROL TO ALLYL COMPOUNDS
The present disclosure is directed towards methods of converting glycerol to an allyl compound, involving deoxydehydrating glycerol with formic acid and heat to form allyl alcohol; and esterifying the allyl alcohol with formic acid and/or phthalic anhydride and heat to form allyl formate and diallyl phthalate. In some instances, the heat is generated by a microwave. In further instances, the methods involve polymerizing the allyl alcohol, allyl formate and/or diallyl phthalate to form poly(allyl alcohol) or poly(allyl formate) or poly (diallyl phthalate). In some instances, the allyl polymers were used for the consolidation of oil sands tailings.
Ester-based compound, composition comprising the same, method for preparing the same and resin composition comprising the same
The present invention relates to an ester-based plasticizer composition, a method for preparing the same and a resin composition comprising the same. The ester-based plasticizer composition according to one embodiment of the present invention is a novel terephthalate-based ester compound for a plasticizer prepared through transesterification. When the ester-based plasticizer composition is used in a resin composition, it is capable of providing excellent resistance for stress, and excellent physical properties such as migration resistance and volatility resistance as well as tensile strength and elongation rate.
Anaerobic curable compositions containing blocked (meth)acrylic acid compounds
The present invention relates to anaerobic curable compositions, such as adhesives and sealants, containing blocked acrylic acid compounds. The blocked acrylic acid compounds are labile (meth)acrylic acid compounds having an acetal linkage, which cleaves to release (meth)acrylic acid during anaerobic cure. In this way, the block acrylic acid compounds acts as an adhesion promoter thereby promoting adhesion to various substrates.
Method for polymerising ethylenically unsaturated monomers
The invention relates to a method for polymerizing ethylenically unsaturated monomers by free-radical initiated emulsion polymerization in an aqueous medium in a polymerization reactor, wherein the inside walls and optionally also the fittings in the reactor are coated by applying a deposit-inhibiting product before the reactor is filled, characterized in that the surfaces that are to be coated with deposit-inhibiting product are treated with an acid solution.
Cure accelerators for anaerobic curable compositions
Cure accelerators for anaerobic curable compositions, such as adhesives and sealants, are provided, and which are defined with reference to the compounds shown in structure I ##STR00001##
where A is CH.sub.2 or benzyl, R is C.sub.1-10 alkyl, R is H or C.sub.1-10 alkyl, or R and R taken together may form a four to seven membered ring fused to the benzene ring, R is optional, but when R is present, R is halogen, alkyl, alkenyl, cycloalkyl, hydroxyalkyl, hydroxyalkenyl, alkoxy, amino, alkylene- or alkenylene-ether, alkylene (meth)acrylate, carbonyl, carboxyl, nitroso, sulfonate, hydroxyl or haloalkyl, and EWG is as shown, an electron withdrawing group, such as nitro, nitrile, carboxylate or trihaloalkyl.
Flame-retardant polyhydroxyalkanoate materials
A flame-retardant polyhydroxyalkanoate (PHA) material having a phosphate-terminated side-chain is disclosed.