A sulfur-modified chloroprene polymer latex includes an emulsifier and a sulfur-modified chloroprene polymer obtained by modifying a chloroprene polymer (A) with sulfur (B), wherein the sulfur amount Y in the sulfur-modified chloroprene polymer and the z-average particle size X of the sulfur-modified chloroprene polymer satisfy formulae (1) to (3) (formula (1): 0.10<Y<0.60; formula (2): 120<X<320; and formula (3): Y<0.0025X−0.20), the total amount of a chloroprene monomer (A-1) and a monomer (A-2) copolymerizable with the chloroprene monomer which constitute the chloroprene polymer is 100 parts by mass, the amount of sulfur (B) contained in the sulfur-modified chloroprene polymer is Y parts by mass, and the z-average particle size of the sulfur-modified chloroprene polymer is X nm. The sulfur-modified chloroprene polymer latex composition can also include a metal oxide (C), a cross-linking accelerator (D), and an antioxidant (E).

The invention relates to the composition of core-shell impact modifiers, in particular those with a high T.sub.g core, a low T.sub.g inner shell and a high T.sub.g outer shell, synthesized in such a way to have a unique concentric morphology and/or a combination of high rubber loading and low particle size and/or require only a low surfactant level. The incorporation of these impact modifiers into polymeric compositions allows for a novel combination of high impact while retaining high gloss or a combination of high impact while retaining low haze in the presence of water at elevated temperatures. These impact modifiers also allow excellent efficiency in their use- allowing for excellent impact to be achieved at low loadings.

Aqueous inkjet ink compositions are provided. In an embodiment, such a composition comprises water; resin particles; and a colorant; wherein the resin particles comprise a polymerization product of reactants comprising a monomer, an acidic monomer, a multifunctional monomer, and a reactive surfactant, the resin particles having a D.sub.(z, ave) of no greater than about 150 nm, a D.sub.(v,90) of less than about 200 nm, and a polydispersity index (PDI) of no greater than about 0.050. Methods of forming and using the aqueous inkjet ink compositions are also provided.

Aqueous inkjet ink compositions are provided. In an embodiment, such an aqueous inkjet ink composition comprises water; a high viscosity latex; a colorant; and optionally, a wax. The high viscosity latex comprises water and resin particles comprising a polymerization product of a monomer, an acidic monomer, a hydrophilic monomer, a difunctional monomer, and a reactive surfactant. The high viscosity latex is characterized by a viscosity in a range of from 10 cP to 100 cP as measured at a solid content of 30% and at room temperature. The aqueous inkjet ink composition is free of a water-soluble binder. Methods of forming and using the aqueous inkjet ink compositions are also provided.

An essentially solvent free emulsion is described comprising about 10 parts to about 80 parts of a silicone gum; about 1 part to about 20 parts of an amino-functionalized organopolysiloxane; about 1 part to about 20 parts of a nonionic surfactant; about 0.01 to about 5 parts acid; optionally, a silicone polyether; and optionally, an aqueous solution to equal 100 parts.

The present invention provides a coating composition capable of forming a coating film having a good appearance and design of a coating film and having coating film properties such as scratch resistance with a good balance. Furthermore, the present invention provides a method for forming a multilayer coating film including forming a coating film using the coating composition of the present invention.

An elastomeric article is formed from a blend of nitrile rubber and polychloroprene rubber. The elastomeric article can be a glove, such as a medical exam glove. The elastomeric article is softer than a conventional nitrile elastomeric article. The elastomeric article is formed from a blended rubber latex emulsion of nitrile and polychloroprene. The blended rubber latex emulsion may be free of sulfur and vulcanization accelerators.

Provided is a cellulose derivative composition for a secondary battery binder, a method of preparing a composition for a secondary battery electrode, including the same, and a secondary battery including the same. According to the inventive concept, the cellulose derivative composition for a secondary battery binder may include a compound represented by Formula 1 below.

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The current invention relates to a process for preparing an aqueous binder composition, the process comprising at least the following steps A) and B): A) preparing carboxylic acid-functional vinyl polymer (Polymer A) by emulsion polymerisation of a monomer composition A comprising the following monomers: Ai) at least one carboxylic acid functional olefinically unsaturated monomer; and Aii) at least one olefinically unsaturated monomer different than Ai); B) preparing vinyl polymer (Polymer B) by emulsion polymerization of a monomer composition B in the presence of Polymer A where the monomer composition B comprises the following monomer(s): Bi) at least one olefinically unsaturated monomer; Bii) optionally carboxylic acid functional olefinically unsaturated monomer different than Bi); where at least part of the carboxylic acid groups of Polymer A are deprotonated to obtain ionic or potentially ionic water-dispersing groups; where the acid value of Polymer B is lower than the acid value of Polymer A; where the weight average molecular weight (Mw) of Polymer B is higher than the weight average molecular weight (Mw) of Polymer A; where the glass transition temperature of Polymer B is equal to or lower than that of Polymer A; where the weight ratio of Polymer A to Polymer B is in the range of from 5:95 to 95:5; and whereby step A) comprises at least a first polymerisation stage of a monomer composition A1 effected in the presence of a chain transfer agent C1 having a water solubility of at least 5 g/L and a subsequent second polymerisation stage of a monomer composition A2 effected in the presence of a chain transfer agent C2 having a water solubility of at most 0.5 g/L, and whereby the second polymerisation stage of step A) is effected in the optional further presence of chain transfer agent C1 having a water solubility of at least 5 g/L whereby the concentration of chain transfer agent C1 having a water solubility of at least 5 g/L in the second polymerisation stage of step A) is at most 35 mole-%, relative to the total molar concentration of chain transfer agent C1 and chain transfer agent C2 present in the second polymerisation stage of step A).

A preparation method of calcium peroxide-mediated in situ crosslinkable hydrogel as a sustained oxygen-generating matrix, includes: a) reacting a natural or a synthetic polymer with Traut's reagent (TR) in a solvent, and synthesizing a polymer derivative having thiol group in backbone of the polymer derivative; and b) mixing and reacting a solution of the polymer derivative having thiol group with calcium peroxide (CaO.sub.2), and thereby forming a hydrogel, wherein in the step b), disulfide bonds (—S—S) are induced between backbones of the polymer derivative having thiol group attached by decomposition of calcium peroxide (CaO.sub.2), and thereby in situ crosslinking is formed.