An object of the present invention is to provide a curable resin composition having a low viscosity and capable of obtaining a cured material having excellent compression set. The curable resin composition of the present invention contains the following components (A) to (C): component (A): an oligomer having one or more (meth)acryloyl groups and a polyisobutylene skeleton containing a —[CH2C(CH3)2]—unit, component (B): a monofunctional monomer having a (meth)acryloyloxy group and a saturated heterocycle with a 4 or more membered ring, component (C): a radical polymerization initiator.

This invention relates to a graft copolymer comprising: a) a macromonomer, wherein the macromonomer comprises in polymerized form a first monoethylenically unsaturated monomer selected from a group consisting of esters of methacrylic acid and acrylic acid with straight or branched alcohols having 1 to 3 carbon atoms and no more than 5 mole % an addition fragmentation chain transfer agent; and b) at least one side chain on the macromonomer, wherein the at least one side chain comprises at least 95 wt.-% of acrylic acid in polymerized form,
and its use for improving the dirt pick-up resistance of a paint or coating.

Selected comb polymers include specified amounts of macromonomer and imide functionalization. Further, a method is useful for the preparation of such comb polymers. Lubricant compositions including such comb polymers are useful for reducing wear and fuel consumption of lubricant compositions, especially of engine oil (EO) compositions.

A comb copolymer viscosity modifier may be made by polymerization comprising at least, or consisting essentially of, the following monomers: (a) a hydrogenated polybutadiene-based (alk)acrylate ester macromonomer (which repeat units may comprise from 7.0 wt % to 18 wt % of the repeat units of the comb copolymer viscosity modifier); (b) a C.sub.3-C.sub.8 alkyl (alk)acrylate ester monomer (which repeat units may comprise from 40 wt % to 71 wt % or from 45 wt % to 64 wt % of the repeat units of the comb copolymer viscosity modifier); and (c) a C.sub.12-C.sub.24 alkyl (alk)acrylate ester monomer, wherein repeat units based on the C.sub.12-C.sub.24 alkyl (alk)acrylate ester monomer comprise at least 21.0 wt % (and optionally up to 35.0 wt %) of repeat units of the comb copolymer viscosity modifier. Lubricant compositions comprising the comb copolymer viscosity modifier, as well as uses thereof and methods for modifying viscosity, are also contemplated herein.

A comb copolymer viscosity modifier may be made by polymerization comprising at least, or consisting essentially of, the following monomers: (a) (optionally from 7.0 wt % to 18 wt %, by repeat units, of) a hydrogenated polybutadiene-based (alk)acrylate ester macromonomer; (b) (optionally from 33 wt % to 64 wt %, by repeat units, of) a C.sub.3-C.sub.8 alkyl (alk)acrylate ester monomer; (c) a C.sub.12-C.sub.24 alkyl (alk)acrylate ester monomer; and (d) (optionally from 3.0 wt % to 25 wt %, by repeat units, of) H-endcapped, C.sub.1-C.sub.18 alkyl-endcapped, or C.sub.6-C.sub.20 aryl-, aralkyl-, or alkaryl-endcapped C.sub.2-C.sub.6 oxyalkyl or C.sub.2-C.sub.6 oligo(alkylene glycol)-based (alk)acrylate ester monomer, wherein repeat units based on monomer (c) and/or monomer (d) comprise at least 21.0 wt % (and optionally up to 35.0 wt %) of repeat units of the comb copolymer viscosity modifier. Lubricant compositions comprising the comb copolymer viscosity modifier, as well as uses thereof and methods for modifying viscosity and dispersancy, are also contemplated.

A comb polymer can be used for reducing a Noack evaporation loss of a lubricant composition, especially of an engine oil composition. Application of the comb polymer to the lubricant composition can bring about the desired reduction. The comb polymer can include specified amounts of macromonomer and alkyl acrylates. Resulting lubricant compositions can include the comb polymer.

A composition comprising vinyl-terminated polyethylene having an Mn from about 200 g/mol to about 10,000 g/mol; and a comb polyolefin having polyethylene arms attached to a random copolymer backbone, said backbone including units derived from an alpha-olefin having 3 or more carbon atoms, where the polyethylene arms have an Mn from about 200 g/mol to about 10,000 g/mol, and where the comb polyolefin has an Mp from about 7,500 to about 400,000 g/mol.

An additive manufacturing composition for powder bed processes is described. The composition includes at least a first type of impact modified polymer beads. The polymer beads include a) an acrylic or vinyl (co)polymer matrix, and b) an impact modifier in which at least 85% w/w of the first type of impact modified polymer beads have a particle size of between ≥20 μm and ≤200 μm and/or on average the impact modified polymer beads have greater than 5% w/w impact modifier. Also disclosed is an additive manufacturing process for a production of a three dimensional product comprising fused impact modified polymer particles. The use of a composition in additive manufacturing, an additive manufacturing cartridge or replacement hopper and a process for the production of impact modified polymer beads by a suspension polymerization process is also disclosed.

Thermoplastic elastomer compositions comprising acrylic multigraft copolymers are described. The multigraft copolymers comprise a rubbery polyacrylate backbone and a plurality of randomly spaced glassy polyacrylate side chains. The multigraft copolymers can be prepared using a facile grafting through method that can provide copolymers with enhanced purity. The acrylic multigraft copolymers exhibit microphase separated morphologies and “superelastomeric” properties, including an elongation at break, strain at break, and/or strain recovery behavior that exceeds that of conventional triblock copolymer polyacrylate thermoplastic elastomers.

An example of a bottlebrush polymer has a polymer backbone and a plurality of individual brush moieties bonded to the polymer backbone. The individual brush moieties include a ketone, a hydrophilic segment, and a surface adhesive terminal group. The brush moieties can be functionalized and/or cross-linked.