The present application is relates to a pressure-sensitive adhesive composition. The pressure-sensitive adhesive composition of the present application may form a pressure-sensitive adhesive having excellent durability and reliability, stress relaxation and reworkability. In addition, when the pressure-sensitive adhesive composition is used collaterally, for example, a coating process may be efficiently performed even when a coating solid content is high, thereby maintaining excellent productivity and forming a pressure-sensitive adhesive having excellent uniformity in thickness. The pressure-sensitive adhesive composition may be used for an optical film such as a polarizing plate.

A molded product with excellent transparency can be obtained by using a polymer (D) obtained by suspension polymerization of a monomer mixture (1) containing (a) to (c) below: (a) 5-60 mass % of a specific macromonomer; (b) 5-60 mass % of the raw material monomer of a homopolymer (B) that has a solubility parameter that is different by 0.25 or more from the solubility parameter of the macromonomer (a); and (c) 10-80 mass % of the raw material monomer of a homopolymer (C) that has a solubility parameter that is different by less than 0.25 from the solubility parameter of macromonomer (a).

A molded product with excellent transparency can be obtained by using a polymer (D) obtained by suspension polymerization of a monomer mixture (1) containing (a) to (c) below: (a) 5-60 mass % of a specific macromonomer; (b) 5-60 mass % of the raw material monomer of a homopolymer (B) that has a solubility parameter that is different by 0.25 or more from the solubility parameter of the macromonomer (a); and (c) 10-80 mass % of the raw material monomer of a homopolymer (C) that has a solubility parameter that is different by less than 0.25 from the solubility parameter of macromonomer (a).

A modified acrylic block copolymer is obtained by a method comprising subjecting a block copolymer (C) to a reaction with an amine compound, wherein the block copolymer comprises a polymer block (A) comprising a (meth)acrylic acid ester unit (a) and a polymer block (B′) comprising a (meth)acrylic acid ester unit (b′), the (meth)acrylic acid ester unit (a) is structurally different from the (meth)acrylic acid ester unit (b′), thereby partly or entirely converting the (meth)acrylic acid ester unit (b′) into at least one selected from the group consisting of an N-substituted (meth)acrylamide unit (d), a (meth)acrylic acid unit (c), and an N-substituted bis((meth)acryl)amide unit (e).

A modified acrylic block copolymer is obtained by a method comprising subjecting a block copolymer (C) to a reaction with an amine compound, wherein the block copolymer comprises a polymer block (A) comprising a (meth)acrylic acid ester unit (a) and a polymer block (B′) comprising a (meth)acrylic acid ester unit (b′), the (meth)acrylic acid ester unit (a) is structurally different from the (meth)acrylic acid ester unit (b′), thereby partly or entirely converting the (meth)acrylic acid ester unit (b′) into at least one selected from the group consisting of an N-substituted (meth)acrylamide unit (d), a (meth)acrylic acid unit (c), and an N-substituted bis((meth)acryl)amide unit (e).

Methods are generally provided for preparing a polymeric composition that includes a grafted block copolymer. Methods are also generally provided for preparing a polymeric composition that includes a star block copolymer prepared from a central core molecule that includes a plurality of attachment moieties. Methods are also generally provided for preparing a polymeric composition that includes a linear block copolymer. Block copolymers are also generally provided. Multi-segmented linear block copolymers are also generally provided.

There is provided a method of manufacturing an electrophoretic particle, in which the electrophoretic particle includes a mother particle and a block copolymer, including: a step of polymerizing a monomer M having a site contributing to dispersibility into a dispersion medium, a monomer M including a second functional group having reactivity with the first functional group, a charged monomer M by living polymerization without random copolymerizing the monomer M1 and the monomer M2 so as to obtain the block copolymer; and a step of reacting the first functional group and the second functional group to a bonding section to a mother particle so as to connect the block copolymer to the mother particle.

An example block copolymer may include at least one poly(glucose-6-acrylate) (G6A) block. An example technique may include treating glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) monomer and n-butyl acrylate (nBA) monomer with a free radical initiator in the presence of a chain transfer agent (CTA).

Described are block copolymers which have been prepared by controlled free radical polymerization. Also described is the use of said block copolymers as soil release agents in laundry processes and a process to produce said block copolymers. Further described is a method for easier releasing soil from textiles in laundry processes and a detergent containing said block copolymers.

Graft copolymer polyelectrolyte complexes are disclosed for the efficient delivery of anionic, cationic or polyelectrolyte therapeutic agents into biological cells, and for maintaining the biological activity of these molecules while in serum and other aqueous environments are provided. Such complexes comprise (1) an anionic graft copolymer containing an anionic polymer backbone, with pendent carboxylic acid groups and pendant chains containing amphipathic or hydrophilic polymers covalently bonded to a portion of the pendant carboxylic acid groups, (2) one or more anionic, cationic or polyelectrolyte therapeutic agents, and (3) optionally a liposome optionally containing an additional therapeutic agent. Also disclosed are functional nanoparticles containing the complexes.