Example compliant hydrophilic coatings including a base coat and a lubricious top coat for coating a medical device including a flexible substrate. The coatings exhibit reduced cracking and peeling in response to deformation or expansion of the flexible substrate. Example techniques for coating a medical device including a flexible substrate with compliant hydrophilic coatings.

Example compliant hydrophilic coatings including a base coat and a lubricious top coat for coating a medical device including a flexible substrate. The coatings exhibit reduced cracking and peeling in response to deformation or expansion of the flexible substrate. Example techniques for coating a medical device including a flexible substrate with compliant hydrophilic coatings.

An object of the present invention is to provide an antistatic agent which imparts excellent antistatic properties to thermoplastic resins. The antistatic agent of the present invention contains a block polymer (A) having a block of a polyamide (a) and a block of a hydrophilic polymer (b) as structure units; and an amide-forming monomer (c), wherein a weight ratio of the amide-forming monomer (c) to the block polymer (A), i.e., amide-forming monomer (c)/block polymer (A), is 2/98 to 12/88.

The present invention describes compounds and uses thereof in applications relating to absorption of electromagnetic energy. Preferred compounds are double bond-containing compounds capable of absorbing electromagnetic radiation energy and having improved properties.

The present invention describes compounds and uses thereof in applications relating to absorption of electromagnetic energy. Preferred compounds are double bond-containing compounds capable of absorbing electromagnetic radiation energy and having improved properties.

The present invention relates to a multi-aziridine compound having: a) at least 2 of the following structural units (A) whereby R.sub.1 is H; R.sub.2 and R.sub.4 are independently chosen from H, a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; R.sub.3 is chosen from a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; or R.sub.2 and R.sub.3 (in case R.sub.2 is different than H) may be part of the same cyclic group containing from 3 to 8 carbon atoms; R′ and R″ are independently H or an aliphatic hydrocarbon group containing from 1 to 12 carbon atoms; and b) a molecular weight of at least 600 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry according to the description.

The present invention relates to a multi-aziridine compound having: a) at least 2 of the following structural units (A) whereby R.sub.1 is H; R.sub.2 and R.sub.4 are independently chosen from H, a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; R.sub.3 is chosen from a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; or R.sub.2 and R.sub.3 (in case R.sub.2 is different than H) may be part of the same cyclic group containing from 3 to 8 carbon atoms; R′ and R″ are independently H or an aliphatic hydrocarbon group containing from 1 to 12 carbon atoms; and b) a molecular weight of at least 600 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry according to the description.

The present disclosure relates to a precursor composition of a pressure sensitive adhesive comprising: a) a (co)polymeric base component having a weight-average molecular weight (M.sub.w) no greater than 500,000 g/mol and comprising at least one reactive functional group (X); and b) a multi-functional oligomeric branching compound comprising an oligomer backbone and having a weight-average molecular weight (M.sub.w) greater than 250 g/mol, wherein the multi-functional oligomeric branching compound comprises at least two complementary reactive functional groups (Y) which are capable of chemically reacting with the at least one reactive functional group (X) of the (co)polymeric base component.

The present disclosure relates to a precursor composition of a pressure sensitive adhesive comprising: a) a (co)polymeric base component having a weight-average molecular weight (M.sub.w) no greater than 500,000 g/mol and comprising at least one reactive functional group (X); and b) a multi-functional oligomeric branching compound comprising an oligomer backbone and having a weight-average molecular weight (M.sub.w) greater than 250 g/mol, wherein the multi-functional oligomeric branching compound comprises at least two complementary reactive functional groups (Y) which are capable of chemically reacting with the at least one reactive functional group (X) of the (co)polymeric base component.

The present invention relates to aqueous acrylic polymer latexes, which are suitable as binders in coating compositions for providing flexible roofing. The present invention also relates to coating compositions containing such binders, which are suitable for providing flexible roofing. The aqueous acrylic polymer latexes have a glass transition temperature T.sub.g of at most from −10° C., in particular at most −20° C., or, in case of a multi-stage polymer latex a weight average glass transition temperature T.sub.g of at most from −10° C., where the polymer of the acrylic polymer latex has a carbon polymer backbone formed by polymerized ethylenically unsaturated monomers M comprising acrylic monomers, and where the carbon polymer backbone bears functional groups of the formula (I) attached to carbon atoms of the polymer backbone *—C(═O)—O-[A-NH].sub.nH (I) where the asterisk indicates the atom attached to a carbon atom of the polymer backbone, n is an integer, the number average of n in all functional groups of the formula (I) being >1, in particular at least 1.1 or at least 1.2 or at least 1.3, and A is selected from the group consisting of 1,2-ethandiyl or 1,2-propandiyl, where the functional groups of the formula (I) contribute to the total weight of the polymer in the acrylic polymer latex by 0.1 to 10% by weight.