C09J175/02

FLEXIBLE POLYUREAS FOR FLEXIBLE PACKAGING ADHESIVE WITHOUT AROMATIC AMINE MIGRATION
20210040362 · 2021-02-11 ·

Provided is an adhesive comprising a reaction product of (A) an aliphatic polyisocyanate having a molecular weight of from 132 to 700; and (B) a polyaspartate comprising a reaction product of (B1) a polyamine having a molecular weight of at least 240, and (B2) a Michael addition receptor, wherein viscosity @23 C. according to ASTM D1084-16, remains below 150 cps after four hours, and wherein the adhesive develops an acceptable bond strength to a substrate, defined as having a minimum of 150 g/in. measured @23 C. according to ASTM D 1876-01 or substrate tear, in less than five days after the substrate is laminated with the adhesive. The inventive flexible packaging adhesives are free of aromatic amines and may find use in multilayer laminates for a variety of industries, including the food processing, cosmetics, and detergents industries.

FLEXIBLE POLYUREAS FOR FLEXIBLE PACKAGING ADHESIVE WITHOUT AROMATIC AMINE MIGRATION
20210040362 · 2021-02-11 ·

Provided is an adhesive comprising a reaction product of (A) an aliphatic polyisocyanate having a molecular weight of from 132 to 700; and (B) a polyaspartate comprising a reaction product of (B1) a polyamine having a molecular weight of at least 240, and (B2) a Michael addition receptor, wherein viscosity @23 C. according to ASTM D1084-16, remains below 150 cps after four hours, and wherein the adhesive develops an acceptable bond strength to a substrate, defined as having a minimum of 150 g/in. measured @23 C. according to ASTM D 1876-01 or substrate tear, in less than five days after the substrate is laminated with the adhesive. The inventive flexible packaging adhesives are free of aromatic amines and may find use in multilayer laminates for a variety of industries, including the food processing, cosmetics, and detergents industries.

WORK TIME TO WALK-ON TIME RATIO BY ADDING A PHENOLIC CATALYST TO POLYASPARTIC FLOORING FORMULATIONS
20210032407 · 2021-02-04 · ·

The present invention provides a polyaspartic composition comprising a reaction product of a polyamine and a Michael addition receptor reacted in the presence of a catalyst comprising a phenolic compound, with the proviso that the phenolic compound is not a phenol which is substituted with tert-butyl groups in both ortho positions to the oxygen. Suitable phenolic compounds include phenols, phenolic aldehydes, alkylphenols, benzenediols, cashew nut oil, and combinations thereof. Coatings, adhesives, sealants, composites, castings, and films comprising a polyurea composition may be made by reacting a polyisocyanate with the inventive polyaspartic composition. In particular, floor coatings made with the inventive polyaspartic composition have an elongated work time and a short walk-on time compared to current floor coatings.

AQUEOUS URETDIONE GROUP-CONTAINING COMPOSITIONS AND METHOD FOR PRODUCING SAME

The invention relates to aqueous uretdione group-containing compositions comprising or consisting of (A) at least one uretdione group-containing curing agent based on aliphatic, cycloaliphatic, araliphatic, and/or aromatic polyisocyanates which do not contain chemically bonded hydrophilating groups; (B) at least one hydroxy group-containing polyol which contains at least one chemically bonded carboxylic acid group; (C) optionally solvents; and (D) optionally auxiliary agents and additives; wherein the quantity ratio of the components (A) and (B) is measured such that the molar ratio of the NCO groups of the curing agent (A), said groups being provided in the form of uretdione, to the NCO reactive groups of the polyol (B) equals 3.0:0.5 to 0.5:3.0, and A and B are provided as a physical mixture. The invention additionally relates to a method for producing a polyurethane layer using the aqueous uretdione group-containing composition according to the invention, to the polyurethane layer obtained therefrom, and to a substrate which is coated with or adhered to the polyurethane layer.

CATALYST SYSTEM FOR URETDIONE DISPERSIONS

The present invention relates to a catalyst system comprising: A) at least one compound selected from azoles, oxazoles, thiazoles, benzotriazole, benzimidazole, benzoxazole and salts thereof; B) at least one acid catcher, which contains at least one epoxy group; and C) at least one catalyst containing an N,N,N-trisubstituted amidine structure with an amidine group content of from 12.0 to 47.0 wt %, calculated as CN2 with molecular weight=40. The invention also relates to a kit which comprises the catalyst system of the present invention and an aqueous uretdione dispersion having an acid number of from 1 to 100 KOH/g and additionally at least one carboxyl group. The invention further relates to a method for producing a polyurethane layer using the catalyst system of the present invention and said uretdione dispersion, and to the obtained polyurethane layer, and to the use of the catalyst system for curing aqueous acidic uretdione dispersions and/or for the production of paints or coatings.

URETDIONE-CONTAINING POLYURETHANE-DISPERSIONS COMPRISING HYDROPHILIC GROUPS

The present invention relates to a specific uretdione prepolymer, and an aqueous curable composition based on the specific uretdione prepolymer. Furthermore, it pertains to a process for curing said aqueous curable composition, the cured article obtained by this process and additionally to the use of said aqueous composition for coatings, adhesives and/or sealants.

AQUEOUS URETDIONE GROUP-CONTAINING COMPOSITIONS AND METHOD FOR PRODUCING SAME

The invention relates to aqueous uretdione group-containing compositions comprising or consisting of (A) at least one uretdione group-containing curing agent based on aliphatic, cycloaliphatic, aliphatic and/or aromatic polyisocyanates which do not contain chemically bonded hydrophilating groups; (B) at least one polyacrylate copolymer; (C) optionally solvents; and (D) optionally auxiliary agents and additives; wherein the quantity ratio of the components (A) and (B) is measured such that the molar ratio of the NCO groups of the curing agent (A), said groups being provided in the form of uretdione, to the NCO reactive groups of the polyacrylate copolymer (B) equals 3.0:0.5 to 0.5:3.0, and A and B are provided as a physical mixture. The invention additionally relates to a method for producing a polyurethane layer using the aqueous uretdione group-containing composition according to the invention, to the polyurethane layer obtained therefrom, and to a substrate which is coated with or adhered to the polyurethane layer.

ADMIXED MODIFIERS FOR ADHESIVES

Disclosed is a method for improving interfacial adhesion of an adhesive to unprimed substrates and an improved adhesive composition, involving admixing an adhesive with an adhesive modifier, where the modifier is at least partially soluble in the at least one adhesive and includes either a non-aromatic polyol or a molecule having at least one ortho-hydroxyl substitution on a benzene ring.

ADMIXED MODIFIERS FOR ADHESIVES

Disclosed is a method for improving interfacial adhesion of an adhesive to unprimed substrates and an improved adhesive composition, involving admixing an adhesive with an adhesive modifier, where the modifier is at least partially soluble in the at least one adhesive and includes either a non-aromatic polyol or a molecule having at least one ortho-hydroxyl substitution on a benzene ring.

Adhesive based on a special polyurethaneurea with adjustable bonding force, and production and use thereof

The present invention relates to an adhesive producible from an aqueous polyurethaneurea dispersion comprising an amorphous polyurethaneurea (V1) obtainable by reacting at least A) one aliphatic, cycloaliphatic or araliphatic polyisocyanate component having an average isocyanate functionality of 1.8 and 2.6, B) one polyetherpolyol component, C) one amino-functional chain extender component having at least 2 isocyanate-reactive amino groups, containing at least one amino-functional compound C1) that does not have any ionic or ionogenic groups and/or an amino-functional compound C2) that has ionic or ionogenic groups, D) optionally further hydrophilizing components different than C2), E) optionally hydroxy-functional compounds having a molecular weight of 62 to 399 mol/g, F) optionally further polymeric polyols that are different than B), G) optionally one compound having exactly one isocyanate-reactive group or one compound having more than one isocyanate-reactive group, where only one of the isocyanate-reactive groups reacts with the isocyanate groups present in the reaction mixture under the reaction conditions chosen, and H) optionally one aliphatic, cycloaliphatic or araliphatic polyisocyanate component having an average isocyanate functionality of >2.6 and 4, where components B) and F) together contain 30% by weight of component F), based on the total mass of components B) and F) and a hydrophilic polyisocyanate (V2) preparable at least from the components of I) an aliphatic, cycloaliphatic or araliphatic polyisocyanate component having an average isocyanate functionality of preferably 2.0 and 3.6, J) a polymeric, hydrophilic and monofunctional polyalkylene oxide component, K) optionally further hydrophilizing components different than J), L) optionally admixtures and auxiliaries. The invention likewise provides an adhesive layer and a product including the adhesive, a process for producing the adhesive layer, a specific polyurethaneurea, and the use of the adhesive and a kit having components (V1) and (V2).