The present invention provides a graft copolymer comprising: (a) a hydrophobic functional polymeric backbone, wherein the backbone comprises (i) an acrylate polymer, an alkylacrylate polymer, or both an acrylate polymer and an alkylacrylate polymer, wherein the backbone has an average molecular weight (M) of from about 3,000 to about 100,000; and (b) a plurality of hydrophilic polymeric side chains attached to the hydrophobic functional polymeric backbone, wherein the hydrophilic polymeric side chains comprise a polymerization product of at least one polymerizable unsaturated monomer and a polymerizable amine-containing unsaturated monomer.

Functionalized zwitterionic and mixed charge polymers and copolymers, methods for making the polymers and copolymers, hydrogels prepared from the functionalized zwitterionic and mixed charge polymers and copolymers, methods for making and using the hydrogels, and zwitterionic and mixed charge polymers and copolymers for administration for therapeutic agents.

The invention relates to a process for preparing a graft copolymer comprising polyethylene, comprising the steps of: A) providing an ethylene copolymer comprising side chains having CC bond and B) reacting the ethylene copolymer of step A) with an azide compound in the presence of a catalyst, a free radical initiator or diphenylamine to obtain the graft copolymer, wherein the azide compound is an azide compound having a functional group or a polymer having an azide group.

Directed self-assembly (DSA) using block copolymers (BCPs) is emerging as a viable alternative to photolithography for creating features 10 nm and smaller. Block copolymers with balanced surface energy between the polymer blocks, tunable , and tunable glass transition temperatures (T.sub.g) have been formulated. The block copolymers can achieve perpendicular orientation by simple thermal annealing due to the surface energy balance between the polymer blocks, which allows avoiding solvent annealing or top-coat. The value can be tuned up to achieve L.sub.0 as low as 12 nm for lamellar-structured BCPs and hole/pillar size as small as 6 nm for cylinder-structured BCPs. The Tg of the BCPs can also be tuned to lower than those of PS-b-PMMA standards. The enhanced polymer chain mobility resulting from the decreased Tg of the block copolymer may help with improving the kinetics of BCP self-assembly during the thermal annealing.

Crosslinkable interpolymer blends comprising ethylene monomer residues, residues of comonomers having carboxylic acid and/or carboxylic acid anhydride functionality, and residues of comonomers having epoxide functionality, a peroxide initiator, and optionally a crosslinking catalyst, which, in embodiments, cure to a gel content of greater than (>) 50 wt % within less than 1.5 minutes at 200C, and require little or no degassing after crosslinking.

The present invention relates generally to polyelectrolyte-layer forming block copolymers adsorbed at colloid interfaces in aqua solution and compositions and uses thereof. In particular, the present invention relates to agricultural material compositions comprising particles of at least one agricultural material and a polyelectrolyte-layer forming block copolymer. The present invention also relates to non-agricultural material compositions comprising particles of at least one non-agricultural material and a polyelectrolyte-layer forming block co-polymer.

A method of producing a structure containing a phase-separated structure, the method including: applying a brush composition to a substrate to form a brush layer; forming a layer containing a block copolymer on the brush layer; and phase-separating the layer containing the block copolymer, the brush composition including a resin component (A), the resin component (A) containing a polymeric compound (A1) in which a first polymer block and a second polymer block are bonded to each other through a linking group containing a substrate adhering group.

A water-absorbing resin having a high swollen gel elastic modulus, a high swelling capacity and a method for producing the same are provided where the water-absorbing resin includes a water soluble unsaturated monomer having a dissociable group, an internal crosslinked structure index expressed by the following numerical formula of 14 or more, a weight average molecular weight (Mw) after a hydrolysis treatment of 220,000 or less, and a molecular weight distribution (Mw/Mn) after a hydrolysis treatment of 3.40 or less: Crosslinked structure index=(Equilibrium swelling capacity with respect to 0.9 wt % physiological saline solution.sup.1/3/(Weight average molecular weight (Mw) after hydrolysis treatment)1000000; where the hydrolysis treatment leaves 50 mg of the water-absorbing resin as a solids content to stand still in 10 g of a 0.1 mol/l aqueous sodium hydroxide solution for 3 weeks at 80 C., and the weight average molecular weight (Mw) is measured after the treatment.

A polyacrylate-polyolefin copolymer and composition for volatile solvent-free coating comprising such compounds having the following structure: ##STR00001##
wherein PO is a polyolefin having a number average molecular weight of at least 300 g/mole, and Ar is selected from the group consisting of C6 to C20 aryls, a C7 to C32 alkylaryls, a C6 to C20 aryloxys, and halogen substituted C6 to C20 aryls and C7 to C32 alkylaryls, while the other variables are as described herein. The copolymers can be produced in an alkylation reaction between the desired polyacrylate and a vinyl/vinylidene-terminated polyolefin.

The present application may provide a block copolymer and a use thereof. The present application may provide a block copolymer and a use thereof. The block copolymer of the present application may have excellent self-assembly properties or phase separation characteristics and simultaneously have characteristics capable of changing the self-assembly structure formed once, or provide a block copolymer capable of forming a pattern of phase separation structures in a polymer membrane.